Preliminary Report on U-Th-Pb Isotope Systematics of the Olivine-Phyric Shergottite Tissint

NASA Technical Reports Server (NTRS)

Moriwaki, R.; Usui, T.; Yokoyama, T.; Simon, J. I.; Jones, J. H.

2014-01-01

Geochemical studies of shergottites suggest that their parental magmas reflect mixtures between at least two distinct geochemical source reservoirs, producing correlations between radiogenic isotope compositions, and trace element abundances.. These correlations have been interpreted as indicating the presence of a reduced, incompatible-element- depleted reservoir and an oxidized, incompatible-element-rich reservoir. The former is clearly a depleted mantle source, but there has been a long debate regarding the origin of the enriched reservoir. Two contrasting models have been proposed regarding the location and mixing process of the two geochemical source reservoirs: (1) assimilation of oxidized crust by mantle derived, reduced magmas, or (2) mixing of two distinct mantle reservoirs during melting. The former clearly requires the ancient martian crust to be the enriched source (crustal assimilation), whereas the latter requires a long-lived enriched mantle domain that probably originated from residual melts formed during solidification of a magma ocean (heterogeneous mantle model). This study conducts Pb isotope and U-Th-Pb concentration analyses of the olivine-phyric shergottite Tissint because U-Th-Pb isotope systematics have been intensively used as a powerful radiogenic tracer to characterize old crust/sediment components in mantle- derived, terrestrial oceanic island basalts. The U-Th-Pb analyses are applied to sequential acid leaching fractions obtained from Tissint whole-rock powder in order to search for Pb isotopic source components in Tissint magma. Here we report preliminary results of the U-Th-Pb analyses of acid leachates and a residue, and propose the possibility that Tissint would have experienced minor assimilation of old martian crust.

Two-component mantle melting-mixing model for the generation of mid-ocean ridge basalts: Implications for the volatile content of the Pacific upper mantle

NASA Astrophysics Data System (ADS)

Shimizu, Kei; Saal, Alberto E.; Myers, Corinne E.; Nagle, Ashley N.; Hauri, Erik H.; Forsyth, Donald W.; Kamenetsky, Vadim S.; Niu, Yaoling

2016-03-01

We report major, trace, and volatile element (CO2, H2O, F, Cl, S) contents and Sr, Nd, and Pb isotopes of mid-ocean ridge basalt (MORB) glasses from the Northern East Pacific Rise (NEPR) off-axis seamounts, the Quebrada-Discovery-GoFar (QDG) transform fault system, and the Macquarie Island. The incompatible trace element (ITE) contents of the samples range from highly depleted (DMORB, Th/La ⩽ 0.035) to enriched (EMORB, Th/La ⩾ 0.07), and the isotopic composition spans the entire range observed in EPR MORB. Our data suggest that at the time of melt generation, the source that generated the EMORB was essentially peridotitic, and that the composition of NMORB might not represent melting of a single upper mantle source (DMM), but rather mixing of melts from a two-component mantle (depleted and enriched DMM or D-DMM and E-DMM, respectively). After filtering the volatile element data for secondary processes (degassing, sulfide saturation, assimilation of seawater-derived component, and fractional crystallization), we use the volatiles to ITE ratios of our samples and a two-component mantle melting-mixing model to estimate the volatile content of the D-DMM (CO2 = 22 ppm, H2O = 59 ppm, F = 8 ppm, Cl = 0.4 ppm, and S = 100 ppm) and the E-DMM (CO2 = 990 ppm, H2O = 660 ppm, F = 31 ppm, Cl = 22 ppm, and S = 165 ppm). Our two-component mantle melting-mixing model reproduces the kernel density estimates (KDE) of Th/La and 143Nd/144Nd ratios for our samples and for EPR axial MORB compiled from the literature. This model suggests that: (1) 78% of the Pacific upper mantle is highly depleted (D-DMM) while 22% is enriched (E-DMM) in volatile and refractory ITE, (2) the melts produced during variable degrees of melting of the E-DMM controls most of the MORB geochemical variation, and (3) a fraction (∼65% to 80%) of the low degree EMORB melts (produced by ∼1.3% melting) may escape melt aggregation by freezing at the base of the oceanic lithosphere, significantly enriching it in volatile and trace element contents. Our results are consistent with previously proposed geodynamical processes acting at mid-ocean ridges and with the generation of the E-DMM. Our observations indicate that the D-DMM and E-DMM have (1) a relatively constant CO2/Cl ratio of ∼57 ± 8, and (2) volatile and ITE element abundance patterns that can be related by a simple melting event, supporting the hypothesis that the E-DMM is a recycled oceanic lithosphere mantle metasomatized by low degree melts. Our calculation and model give rise to a Pacific upper mantle with volatile content of CO2 = 235 ppm, H2O = 191 ppm, F = 13 ppm, Cl = 5 ppm, and S = 114 ppm.

The role of water in the petrogenesis of Marina trough magmas

NASA Astrophysics Data System (ADS)

Stolper, Edward; Newman, Sally

1994-02-01

Most variations in composition among primitive basalts from the Mariana back-arc trough can be explained by melting mixtures of an N-type mid-ocean ridge basalt (NMORB) mantle source and an H2O rich component, provided the degree of melting is positively and approximately linearly correlated with the proportion of the H2O-rich component in the mixture. We conclude that the degrees of melting by which Mariana trough magmas are generated increase from magmas similar to NMORB, through more H2O-enriched basalts, to 'arc-like' basalts, and that this increase is due to the lowering of the solidus of mantle peridotite that accompanies addition of the H2O-rich component. The H2O-rich component is likely to be ultimately derived from fluid from a subducting slab, but we propose that by the time fluids reach the source regions of Mariana trough basalts, they have interacted with sufficient mantle material that for all but the most incompatible of elements (with respect to fluid-mantle interaction), they are in equilibrium with the mantle. In contrast, fluids added to the source regions of Mariana island-arc magmas have typically interacted with less mantle and thus retain the signature of slab-derived fluids to varying degrees for all but the most compatible elements. Primitive Mariana arc basalts can be generated by melting mixtures of such incompletely exchanged slab-derived fluids and sources similar to NMORB-type mantle sources, but the degrees of melting are typically higher than those of Mariana trough NMORB and the sources have been variably depleted relative to the back-arc sources by previous melt extraction. This depletion may be related to earlier extraction of back-arc basin magmas or may evolve by repeated fluxing of the sources as fluid is continually added to them in the regions of arc magma generation. If fluid with partitioning behavior relative to the solid mantle similar to that deduced for the H2O-rich component involved in the generation of Mariana trough basalts were extracted from primitive mantle, the residual mantle would have many of the minor and trace element characteristics of typical oceanic upper mantle; primitive mantle enriched in such fluid would be a satisfactory source for the continental crust in terms of its trace and minor element chemical composition.

The importance of mantle wedge heterogeneity to subduction zone magmatism and the origin of EM1

NASA Astrophysics Data System (ADS)

Turner, Stephen J.; Langmuir, Charles H.; Dungan, Michael A.; Escrig, Stephane

2017-08-01

The composition of the convecting asthenospheric mantle that feeds the mantle wedge can be investigated via rear-arc lavas that have minimal slab influence. This "ambient mantle wedge" composition (the composition of the wedge prior to the addition of a slab component) varies substantially both worldwide and within individual arcs. 143Nd/144Nd measurements of rear-arc samples that have minimal slab influence are similar to 143Nd/144Nd in the stratovolcanoes of the adjacent volcanic fronts, suggesting that 143Nd/144Nd of arc-front volcanics are largely inherited from the ambient mantle composition. 143Nd/144Nd correlates with ratios such as Th/U, Zr/Nb, and La/Sm, indicating that these ratios also are strongly influenced by ambient wedge heterogeneity. The same phenomenon is observed among individual volcanoes from the Chilean Southern Volcanic Zone (SVZ), where along-strike variability of the volcanic front tracks that of rear-arc monogenetic volcanics. Depleted mantle wedges are more strongly influenced by slab-derived components than are enriched wedges. This leads to surprising trace element correlations in the global dataset, such as between Pb/Nb and Zr/Nb, which are not explicable by variable compositions or fluxes of slab components. Depleted ambient mantle is present beneath arcs with back-arc spreading; relatively enriched mantle is present adjacent to continents. Ambient mantle wedge heterogeneity both globally and regionally forms isotope mixing trajectories for Sr, Nd and Hf between depleted mantle and EM1-type enriched compositions as represented by Gough Island basalts. Making use of this relationship permits a quantitative match with the SVZ data. It has been suggested that EM1-type mantle reservoirs are the result of recycled lower continental crust, though such models do not account for certain trace element ratios such as Ce/Pb and Nb/U or the surprisingly homogeneous trace element compositions of EM1 volcanics. A model in which the EM1 end-member found in continental arcs is produced by low-degree melt-metasomatism of the sub-continental lithospheric mantle may be more plausible. The 143Nd/144Nd maximum along the SVZ may be a consequence of either rifting and collision of two ancient lithospheric domains or a slab tear. The correspondence of mantle wedge variations with EM1 suggests a potential role for metasomatized sub-continental lithosphere in creating EM1 sources globally.

Volatile element content of the heterogeneous upper mantle

NASA Astrophysics Data System (ADS)

Shimizu, K.; Saal, A. E.; Hauri, E. H.; Forsyth, D. W.; Kamenetsky, V. S.; Niu, Y.

2014-12-01

The physical properties of the asthenosphere (e.g., seismic velocity, viscosity, electrical conductivity) have been attributed to either mineral properties at relevant temperature, pressure, and water content or to the presence of a low melt fraction. We resort to the geochemical studies of MORB to unravel the composition of the asthenosphere. It is important to determine to what extent the geochemical variations in axial MORB do represent a homogeneous mantle composition and variations in the physical conditions of magma generation and transport; or alternatively, they represent mixing of melts from a heterogeneous upper mantle. Lavas from intra-transform faults and off-axis seamounts share a common mantle source with axial MORB, but experience less differentiation and homogenization. Therefore they provide better estimates for the end-member volatile budget of the heterogeneous upper mantle. We present major, trace, and volatile element data (H2O, CO2, Cl, F, S) as well as Sr, Nd, and Pb isotopic compositions [1, 2] of basaltic glasses (MgO > 6.0 wt%) from the NEPR seamounts, Quebrada-Discovery-Gofar transform fault system, and Macquarie Island. The samples range from incompatible trace element (ITE) depleted (DMORB: Th/La<0.035) to enriched (EMORB: Th/La>0.07) spanning the entire range of EPR MORB. The isotopic composition of the samples correlates with the degree of trace element enrichment indicating long-lived mantle heterogeneity. Once shallow-level processes (degassing, crystallization, and crustal assimilation) have been considered, we conducted a two-component (DMORB- and EMORB-) mantle melting-mixing model. Our model reproduces the major, trace and volatile element contents and isotopic composition of our samples and suggests that (1) 90% of the upper mantle is highly depleted in ITE (DMORB source) with only 10% of an enriched component (EMORB source), (2) the EMORB source is peridotitic rather than pyroxenitic, and (3) NMORB do not represent an actual mantle source, but the product of magma mixing between D- and E-MORB. Finally we use the volatile to trace element ratios of our samples to estimate the volatile element budget of the end-member components of the upper mantle. [1] Niu, Y. et al. (2002) EPSL, 199, 327-345. [2] Kamenetsky, V. S. et al. (2000) J. Petrology, 41, 411-430.

HIMU-type Mid-Ocean Ridge Basalts Incorporate a Primitive Component

NASA Astrophysics Data System (ADS)

Tucker, J.; Mukhopadhyay, S.; Schilling, J. E.

2011-12-01

Samples from 5°N to 7°S along the MAR axis span a range of compositions from depleted MORB (La/SmN ~0.5, 206Pb/204Pb ~18) to very enriched MORB (La/SmN ~3, 206Pb/204Pb ~20). The measured 206Pb/204Pb in the enriched samples are among the highest measured MORB values and are thought to represent a HIMU type mantle (high μ where μ is the U/Pb ratio). Therefore, the enriched samples provide a unique opportunity to characterize the heavy noble gas composition of the HIMU mantle. If HIMU mantle is related to recycled crust, then the noble gas measurements can also provide insights into recycling of atmospheric noble gases back into the mantle. Additionally, the depleted equatorial samples provide an opportunity to characterize the Ar and Xe composition of the N-MORB source for comparison to the 14°N E-MORB popping rock. Finally, the large variations in lithophile isotopes over a geographically short distance affords the opportunity to study the nature of coupling between the noble gases and lithophile tracers, and understand the origin of the heterogeneities in the MORB source. Stepwise crushing and rare gas analysis (He, Ne, Ar, Xe) was undertaken for both enriched and depleted samples. Many of the crushing steps yielded 20Ne/22Ne > 12, and good correlations between Ne, Ar, and Xe isotopes allow for mantle source compositions of Ar and Xe to be determined by extrapolating the measured values to a mantle 20Ne/22Ne of 12.5. The highest measured values of Ar and Xe in a depleted N-MORB are comparable to measured values of the E-MORB popping rock (40Ar/36Ar ~28,000, 129Xe/130Xe ~7.7). When extrapolated to a mantle 20Ne/22Ne of 12.5, the depleted MORB sample indicates a 40Ar/36Ar of ~43,000 (higher than popping rock) and 129Xe/130Xe of ~7.8. Enriched MORB samples from this suite, thought to represent the HIMU mantle, have the same He and Ne characteristics as HIMU basalts from the Cook and Austral Islands; more radiogenic He than MORBs is accompanied by less nucleogenic Ne than MORBs. Additionally, the enriched MORB samples also constrain the HIMU mantle 40Ar/36Ar to ~20,000 and 129Xe/130Xe ~7.3-7.5, significantly lower than the depleted MORBs. Like the HIMU basalts from the Cook and Austral Islands, a less degassed reservoir than the MORB source must be invoked to explain the He and Ne systematics in the HIMU-type MORBs. If HIMU represents recycled crust, then it must have entrained or been entrained by a less degassed mantle from the deep interior. This less degassed reservoir would also explain the good correspondence between low 21Ne/22Ne, low 40Ar/36Ar and low 129Xe/130Xe in the HIMU-type samples. While we cannot rule out recycling of atmospheric noble gases to explain the low 40Ar/36Ar and 129Xe/130Xe, involvement of a source less degassed in He and Ne would also be accompanied by a less degassed Ar and Xe isotopic signature. Therefore the simplest explanation of the covariation between the noble gases and lithophile isotopes involves a mixture of a less processed and hence more primitive component, a degassed recycled component, and depleted MORB mantle beneath the equatorial Mid-Atlantic Ridge.

Geochemical Characterization of Endmember Mantle Components

DTIC Science & Technology

2005-06-01

from the oceanic crust and volcanic edifice beneath Gran Canaria (Canary Islands); consequences for crustal contamination of ascending magmas, Chemical...Enriched Mantle II (EM2) Endmember: Evidence from the Samoan Volcanic Chain .................................................... 19 Abstract...DMM). On the other hand, ocean island basalts (OIBs), erupted by hotspot volcanism , are isotopically heterogeneous in terms of most radiogenic

Constraints on lithosphere-asthenosphere melt mixing in basaltic intraplate volcanism from olivine melt inclusions from southern Payenia, Argentina

NASA Astrophysics Data System (ADS)

Søager, Nina; Portnyagin, Maxim; Hoernle, Kaj; Holm, Paul Martin; Garbe-Schönberg, Dieter

2018-06-01

We present major and trace element compositions of melt inclusions from three alkali basalts from the Río Colorado volcanic field in the Payenia backarc province, Argentina. Modeling of diffusion profiles around the inclusions showed that most inclusions equilibrated <14 days after formation, indicating a short crustal residence time for the magmas and nearly direct ascent through the crust. Despite overlapping host rock isotopic compositions, the inclusions show a large variation in their degree of enrichment, and display trends that we interpret as mixing between asthenospheric OIB-type low K2O-high Nb/U melts and enriched high K2O-low Nb/U lithospheric mantle melts similar in composition to alkaline lamprophyres. The low Nb/U magmas are excessively enriched in the elements Cs, Rb, Ba, Th, U, K, Pb and Cl relative to Nb, Ta and REEs. The enriched low Nb/U components are interpreted to have formed by percolative fractional crystallization of asthenospheric high Nb/U melts in the lithospheric mantle involving crystallization of clinopyroxene, apatite and rutile. The residual fluid-rich melts either mixed directly with new batches of high Nb/U melts or metasomatized and veined the lithospheric mantle which later re-melted during continued volcanism. The major element compositions of the high K2O-low Nb/U components are distinct for the whole rocks and melt inclusions, and most enriched inclusions have lower SiO2 and higher TiO2 contents indicating derivation by melting of amphibole-bearing veins. In contrast, most whole rock low Nb/U basalts have higher SiO2 and lower TiO2 and were most likely formed by melting of pyroxenitic veins or peridotitic metasomatized lithospheric mantle.

Geochemical and petrological evidence of the subduction of delaminated Adriatic continental lithosphere in the genesis of the Neogene-Quaternary magmatism of central Italy

NASA Astrophysics Data System (ADS)

Serri, G.; Innocenti, F.; Manetti, P.

1993-07-01

Serri, G., Innocenti, F. and Manetti, P., 1993. Geochemical and petrological evidence of the subduction of delaminated Adriatic continental lithosphere in the genesis of the Neogene-Quaternary magmatism of central Italy. In: M.J.R. Wortel, U. Hansen and R. Sabadini (Editors), Relationships between Mantle Processes and Geological Processes at or near The Earth's Surface. Tectonophysics, 223: 117-147. The Neogene-Quaternary magmatism of the northern Apenninic arc took place in four phases separated in space and time which become progressively younger from west to east: Phase I, 14 Ma; Phase II, 7.3-6.0 Ma; Phase III, 5.1-2.2 Ma; Phase IV, 1.3-0.1 Ma. This magmatism is the result of the activation of three physically separate sources: (1) the Adriatic continental crust, extracted from the mantle in the late Proterozoic; (2) a strongly refractory, recently K-enriched harzburgitic mantle located in the mechanical boundary layer (MBL) of the lithosphere; and (3) a recently metasomatized, cpx-rich mantle, compositionally variable from Iherzolite to wehrlite-clinopyroxenite, interpreted as an ephemerally K-enriched asthenosphere. The Adriatic continental crust is the dominant source of the acid plutonic and volcanic rocks of the Tuscan region. The acid magmatism is mostly found inside an ellipsoidal area (about 150 × 300 km) centred on Giglio Island, here defined as the Tuscan Crustal Dome. Within this area, mantle-derived magmas unaffected by important crustal contamination processes and mixing with crustal anatectic melts have so far not been found. Pure crustal magmas are rare but are represented, for example by some of the San Vincenzo and Roccastrada rhyolites. Virtually all the Tuscan acid centres show evidence of mixing with potassic mantle-derived magmas. Major and trace elements, as well as {87Sr }/{86Sr } and {143Nd }/{144Nd } data, on primitive rocks (Mg# > 65) reveal two groups of mantle-derived magmas. These define two distinct mantle enrichment trends, both essentially due to the additions of K-rich components which metasomatized separate, compositionally diverse, upper mantle sectors. In both cases the most remarkable mineralogical effect of these enrichment processes is the production of variable amount of phlogopite through reaction between fluids and/or melts with the mantle. The rocks of group I (ol-hy and Q-normative, lamproites, ultrapotassic high-Mg latites, ultrapotassic shoshonites and shoshonites: saturated trend) are considered to be derived by partial melting at low pressure (< 50 km) of strongly (lamproites) to moderately depleted phlogopite harzburgitic sources produced by reaction of residual peridotites with a K-Si-rich, Ca-Sr-poor melt with high ratios of {87Sr }/{86Sr (> 0.717) }, Ce/Sr (> 0.3) and {K 2O }/{Na 2O (> 6-7) }, and low ratios of {143Nd }/{144Nd ( 0.5121-0.5120) } and Ba/La (< 20) ratios; it is proposed that this component was formed by partial melting of subducted carbonate-free material of the upper crustal reservoir (e.g., non-restitic felsic granulites). This material is very common in the central Mediterranean region either as granitoid plutons/terrigenous sediments or as metasedimentary, non-restitic lower crust. The primitive rocks of group II are critically undersaturated, mostly leucitites, tephritic leucitites, leucite basanites, melilitites (undersaturated trend). Experimental petrology suggests that these rocks were formed by partial melting of a variably enriched phlogopite, clinopyroxene-rich mantle at higher pressure than group I primitive magmas. Trace-element modelling indicates that three components were involved in the genesis of group II mantle source: (a) a typical MORB-OIB-like mantle; (b) a component with very high Sr, Ca and Sr/Ce values and very low silica and sodium content, probably carried by a carbonatite melt somehow related to subducted marine carbonates; and (c) a recently added K-rich, Ca-Sr-poor crustal component, relatively well constrained to high {87Sr }/{86Sr (> 0.712) } and {K 2O }/{Na 2O (> 8-9) } values, and low {143Nd }/{144Nd (< 0.51205) }, Ba/La (< 20) and Ce/Sr (> 0.10) ratios. These constraints do not allow to exclude a complete identity between the K-rich components which metasomatized the mantle sources of the saturated and undersaturated trend magmas. The geochemical and isotopic features of the components that metasomatized the mantle sources of the northern Apenninic arc magmatism can be explained by a geodynamic process which causes a large amount of crustal materials to be incorporated within the upper mantle. We propose that the delamination and subduction of the Adriatic continental lithosphere related to the still ongoing northern Apennine continental collision provide a viable mechanism to explain the genesis and eastward discontinuous migration of the magmatism in central Italy. The subduction of delaminated lithospheric mantle with lower crustal slivers would have exposed uppermost mantle (Adriatic MBL) and crustal units previously imbricated in the Apennine chain to the heating advected by the upwelling of a recently and ephemerally K-enriched asthenospheric mantle wedge and by the underplating of magmas derived from it. We consider that the diapiric uprising of a hot, crustally contaminated asthenosphere occurs in the wake left above the sinking of the Adriatic delaminated/subducting continental lithosphere. The delamination/subduction process of the Adriatic lithosphere has probably started in the Early-Middle Miocene, but earlier than 15-14 Ma ago, as indicated by the age and petrologic characteristics of the first magmatic episode (Sisco lamproite) of the northern Apennine orogenesis.

Geochemistry of oceanic carbonatites compared with continental carbonatites: mantle recycling of oceanic crustal carbonate

NASA Astrophysics Data System (ADS)

Hoernle, Kaj; Tilton, George; Le Bas, Mike; Duggen, Svend; Garbe-Schönberg, Dieter

Major and trace element and Sr-Nd-Pb-O-C isotopic compositions are presented for carbonatites from the Cape Verde (Brava, Fogo, Sáo Tiago, Maio and Sáo Vicente) and Canary (Fuerteventura) Islands. Carbonatites show pronounced enrichment in Ba, Th, REE, Sr and Pb in comparison to most silicate volcanic rocks and relative depletion in Ti, Zr, Hf, K and Rb. Calcio (calcitic)-carbonatites have primary (mantle-like) stable isotopic compositions and radiogenic isotopic compositions similar to HIMU-type ocean island basalts. Cape Verde carbonatites, however, have more radiogenic Pb isotope ratios (e.g. 206Pb/204Pb=19.3-20.4) than reported for silicate volcanic rocks from these islands (18.7-19.9 Gerlach et al. 1988; Kokfelt 1998). We interpret calcio-carbonatites to be derived from the melting of recycled carbonated oceanic crust (eclogite) with a recycling age of 1.6 Ga. Because of the degree of recrystallization, replacement of calcite by secondary dolomite and elevated ∂13C and ∂18O, the major and trace element compositions of the magnesio (dolomitic)-carbonatites are likely to reflect secondary processes. Compared with Cape Verde calcio-carbonatites, the less radiogenic Nd and Pb isotopic ratios and the negative Δ7/4 of the magnesio-carbonatites (also observed in silicate volcanic rocks from the Canary and Cape Verde Islands) cannot be explained through secondary processes or through the assimilation of Cape Verde crust. These isotopic characteristics require the involvement of a mantle component that has thus far only been found in the Smoky Butte lamproites from Montana, which are believed to be derived from subcontinental lithospheric sources. Continental carbonatites show much greater variation in radiogenic isotopic composition than oceanic carbonatites, requiring a HIMU-like component similar to that observed in the oceanic carbonatites and enriched components. We interpret the enriched components to be Phanerozoic through Proterozoic marine carbonate (e.g. limestone) recycled through shallow, subcontinental-lithospheric-mantle and deep, lower-mantle sources.

Geochemistry of oceanic carbonatites compared with continental carbonatites: mantle recycling of oceanic crustal carbonate

NASA Astrophysics Data System (ADS)

Hoernle, Kaj; Tilton, George; Le Bas, Mike; Duggen, Svend; Garbe-Schönberg, Dieter

2001-11-01

Major and trace element and Sr-Nd-Pb-O-C isotopic compositions are presented for carbonatites from the Cape Verde (Brava, Fogo, Sáo Tiago, Maio and Sáo Vicente) and Canary (Fuerteventura) Islands. Carbonatites show pronounced enrichment in Ba, Th, REE, Sr and Pb in comparison to most silicate volcanic rocks and relative depletion in Ti, Zr, Hf, K and Rb. Calcio (calcitic)-carbonatites have primary (mantle-like) stable isotopic compositions and radiogenic isotopic compositions similar to HIMU-type ocean island basalts. Cape Verde carbonatites, however, have more radiogenic Pb isotope ratios (e.g. 206Pb/204Pb=19.3-20.4) than reported for silicate volcanic rocks from these islands (18.7-19.9 Gerlach et al. 1988; Kokfelt 1998). We interpret calcio-carbonatites to be derived from the melting of recycled carbonated oceanic crust (eclogite) with a recycling age of 1.6 Ga. Because of the degree of recrystallization, replacement of calcite by secondary dolomite and elevated ∂13C and ∂18O, the major and trace element compositions of the magnesio (dolomitic)-carbonatites are likely to reflect secondary processes. Compared with Cape Verde calcio-carbonatites, the less radiogenic Nd and Pb isotopic ratios and the negative Δ7/4 of the magnesio-carbonatites (also observed in silicate volcanic rocks from the Canary and Cape Verde Islands) cannot be explained through secondary processes or through the assimilation of Cape Verde crust. These isotopic characteristics require the involvement of a mantle component that has thus far only been found in the Smoky Butte lamproites from Montana, which are believed to be derived from subcontinental lithospheric sources. Continental carbonatites show much greater variation in radiogenic isotopic composition than oceanic carbonatites, requiring a HIMU-like component similar to that observed in the oceanic carbonatites and enriched components. We interpret the enriched components to be Phanerozoic through Proterozoic marine carbonate (e.g. limestone) recycled through shallow, subcontinental-lithospheric-mantle and deep, lower-mantle sources.

Origin of geochemical mantle components: Role of spreading ridges and thermal evolution of mantle

NASA Astrophysics Data System (ADS)

Kimura, Jun-Ichi; Gill, James B.; van Keken, Peter E.; Kawabata, Hiroshi; Skora, Susanne

2017-02-01

We explore the element redistribution at mid-ocean ridges (MOR) using a numerical model to evaluate the role of decompression melting of the mantle in Earth's geochemical cycle, with focus on the formation of the depleted mantle component. Our model uses a trace element mass balance based on an internally consistent thermodynamic-petrologic computation to explain the composition of MOR basalt (MORB) and residual peridotite. Model results for MORB-like basalts from 3.5 to 0 Ga indicate a high mantle potential temperature (Tp) of 1650-1500°C during 3.5-1.5 Ga before decreasing gradually to ˜1300°C today. The source mantle composition changed from primitive (PM) to depleted as Tp decreased, but this source mantle is variable with an early depleted reservoir (EDR) mantle periodically present. We examine a two-stage Sr-Nd-Hf-Pb isotopic evolution of mantle residues from melting of PM or EDR at MORs. At high-Tp (3.5-1.5 Ga), the MOR process formed extremely depleted DMM. This coincided with formation of the majority of the continental crust, the subcontinental lithospheric mantle, and the enriched mantle components formed at subduction zones and now found in OIB. During cooler mantle conditions (1.5-0 Ga), the MOR process formed most of the modern ocean basin DMM. Changes in the mode of mantle convection from vigorous deep mantle recharge before ˜1.5 Ga to less vigorous afterward is suggested to explain the thermochemical mantle evolution.

Linking Serpentinite Geochemistry with Possible Alteration and Evolution of Supra-Subduction Wedge Mantle

NASA Astrophysics Data System (ADS)

Scambelluri, M.; Cannaò, E.; Agostini, S.; Gilio, M.

2016-12-01

Serpentinites are able to transport and release volatiles and fluid-mobile elements (FME) found in arc magmas. Constraining the trace element compositions of these rocks and of fluids released by de-serpentinization improves our knowledge of mass transfer from subduction zones to volcanic arcs, and of the role of slab and wedge mantle in this global process. Studies of high-pressure ultramafic rocks exhumed from plate interface settings reveal the fluid/rock interactions atop the slab and the processes that can affect the mantle wedge. Alpine eclogite-facies antigorite serpentinite (Voltri Massif) and fully de-serpentinized meta-peridotite (Cima di Gagnone) are enriched in sediment-derived As, Sb, U, Pb before peak dehydration. Their Sr, Pb and B isotopic compositions are reset during prograde (forearc) interaction with slab fluids. The eclogitic garnet and olivine from the Cima di Gagnone metaperidotite trap primary inclusions of the fluid released during breakdown of antigorite and chlorite. The inclusions display FME enrichments (high Cl, S; variable Cs, Rb, Ba, B, Pb, As, Sb) indicating element release from rocks to fluids during dehydration under subarc conditions. Our studies show that serpentinized mantle rocks from subduction zones sequester FME from slab fluids and convey these components and radiogenic isotopes into the mantle wedge upon dehydration. The geochemical processes revealed by such plate-interface rocks can apply to the supra-subduction mantle. Shallow element release from slabs to mantle wedge, downdrag of this altered mantle and its subsequent (subarc) dehydration transfers crust-derived FMEs to the arc magma sources without the need of concomitant subarc dehydration/melting of metasedimentary slab components. The slab signature detected in arc lavas can thus result from geochemical mixing of sediment, oceanic crust and ultramafic reservoirs into altered wedge-mantle rocks, rather than being attributed to multiple fluids.

Volatile Content of the Mid-ocean Ridge Mantle Inferred from Off-axis Seamounts and Intra-transform Lavas

NASA Astrophysics Data System (ADS)

Shimizu, K.; Saal, A. E.; Hauri, E. H.; Nagle, A.; Forsyth, D. W.; Niu, Y.

2011-12-01

Off-axis seamounts and intra-transform lavas provide more direct geochemical information of the mantle than axial lavas. These smaller volumes of melts undergo lower extent of crystal fractionation and mixing compared to basalts erupting within the ridge axis due to a lack of long-lived magma chambers or along axis melt migration. Therefore, their study provide not only a more reliable approach to determine the volatile content of the intrinsic components forming the Earth's upper mantle, but also help constrain mantle convection, heterogeneity, and crustal recycling. Samples from the Quebrada-Discovery-Gofar (QDG) transform fault system (EPR 3°-5°S) and from northern EPR seamounts (5°-15° N) were collected during KN182-13 (R/V Knorr) and RAIT 02 (R/V Thomas Washington) expeditions, respectively. 159 submarine glasses were analyzed for major elements, trace elements, and volatile elements by triplicate analyses, as well as for Sr and Nd isotopes in a subset of samples. The QDG and northern EPR seamounts have similar trace element and isotopic composition that is consistent with melting of two-component mantle common to both regions. The degree of trace element enrichment (e.g. Th/La), isotopic composition, and depth of melt segregation (e.g. Sm/Yb) have a positive correlation and range from ultra depleted to relatively enriched compositions. In order to investigate the primary volatile content of submarine glasses we first considered shallow level processes, such as volatile degassing, sulfide saturation and interaction of melt with hydrothermally altered material. The vapor-melt equilibrium pressure (Dixon et al., 1995) indicates that the majority of the samples were super-saturated in CO2-H2O vapor at the pressure of eruption, which implies rapid magma ascent rate that prevented complete CO2 degassing. Samples that were sulfide saturated (Liu et al., 2007) and contaminated by seawater or seawater derived material (high Cl/K) were filtered out. F/Nd, Cl/K, and H2O/Ce ratios in our samples positively correlate with Th/La, Sm/Yb, and isotope ratios suggesting that the enriched mantle component is also enriched in volatile contents. S/Dy ratios are the exception, with relatively constant values in both enriched, and depleted basalts. Although it has been argued that correlation between Sr, Nd and Pb isotope ratios and fractionation corrected major element in seamount samples indicate different mantle lithologies under the mid-ocean ridges, we will show that such correlation might be an artifact of ignoring the effect of water during the correction for fractional crystallization. [1] Dixon et al. (1995) J. Pet., 36, 1607-1631. [2] Liu et al. (2007) Geochim Cosmochim Ac., 71, 1783-1799.

Origin of low δ26Mg basalts with EM-I component: Evidence for interaction between enriched lithosphere and carbonated asthenosphere

NASA Astrophysics Data System (ADS)

Tian, H.; Yang, W.; Li, S. G.; Ke, S.; Chu, Z. Y.

2016-12-01

Many studies have focused on the interactions between recycled materials and depleted mantle to explain the origins of EM and HIMU components (e.g., Cohen and O'Nions, 1982; White and Hofmann, 1982). However, little is known about the interactions between recycled materials and enriched mantle and the associated consequences, e.g., late recycled crustal material overprints mantle previously enriched by earlier recycling events of the crust. Recently, light Mg isotopic composition of the basalts from North China Craton (NCC) and South China Block (SCB) has been attributed to recycled carbonate metasomatism from subducted Pacific slab (Yang et al., 2012; Huang et al., 2015). If this explanation is correct, the Cenozoic basalts from Northeast (NE) China should also contain light Mg isotopic compositions. The basalts from NE China have EMI Sr-Nd-Pb isotopic features that are distinct from the NCC and SCB basalts, indicating the contribution of an enriched mantle source (Choi et al., 2006; Chu et al., 2013). Therefore, Mg isotopic compositions of the Cenozoic basalts from NE China will help to determine the interaction between recycled sedimentary carbonates and an enriched mantle. Consistent with the hypothesis, our results show that the Cenozoic basalts from Wudalianchi and Erkeshan, NE China, have homogeneous and light Mg isotopic compositions (δ26Mg =-0.57 to -0.46‰). Based on the similarity to the basalts from NCC and SCB, their light Mg isotopic feature should also be derived from carbonate metasomatism (i.e. carbonated asthenosphere). In addition to that, a question arise that why the interaction between carbonated asthenosphere and the EM-I SLCM significantly modify the trace element and Sr-Nd-Pb isotopic composition of the mantle-derived melt, but have little effect on the Mg isotopes? The possible mechanism is the interaction between low SiO2 melt and peridotite, which converts pyroxene to olivine, as reported in previous studies (e.g., Kelemen et al., 1992; Edwards and Malpas, 1996; Zhou et al., 1996, 2014). During the interaction, the trace elements of the EM-I SCLM largely entered the melt, and all Mg was transferred from Opx and Cpx into the newly formed olivine. Consequently, the Wudalianchi and Erkeshan basalts preserve low δ26Mg and obtain EM-I Sr-Nd-Pb isotopic compositions (Fig. 1).

186Os- 187Os systematics of Gorgona Island komatiites: implications for early growth of the inner core

NASA Astrophysics Data System (ADS)

Brandon, Alan D.; Walker, Richard J.; Puchtel, Igor S.; Becker, Harry; Humayun, Munir; Revillon, Sidonie

2003-02-01

The presence of coupled enrichments in 186Os/ 188Os and 187Os/ 188Os in some mantle-derived materials reflects long-term elevation of Pt/Os and Re/Os relative to the primitive upper mantle. New Os data for the 89 Ma Gorgona Island, Colombia komatiites indicate that these lavas are also variably enriched in 186Os and 187Os, with 186Os/ 188Os ranging between 0.1198397±22 and 0.1198470±38, and with γOs correspondingly ranging from +0.15 to +4.4. These data define a linear trend that converges with the previously reported linear trend generated from data for modern Hawaiian picritic lavas and a sample from the ca. 251 Ma Siberian plume, to a common component with a 186Os/ 188Os of approximately 0.119870 and γOs of +17.5. The convergence of these data to this Os isotopic composition may imply a single ubiquitous source in the Earth's interior that mixes with a variety of different mantle compositions distinguished by variations in γOs. The 187Os- and 186Os-enriched component may have been generated via early crystallization of the solid inner core and consequent increases in Pt/Os and Re/Os in the liquid outer core, with time leading to suprachondritic 186Os/ 188Os and γOs in the outer core. The presence of Os from the outer core in certain portions of the mantle would require a mechanism that could transfer Os from the outer core to the lower mantle, and thence to the surface. If this is the process that generated the isotopic enrichments in the mantle sources of these plume-derived systems, then the current understanding of solid metal-liquid metal partitioning of Pt, Re and Os requires that crystallization of the inner core began prior to 3.5 Ga. Thus, the Os isotopic data reported here provide a new source of data to better constrain the timing of inner core formation, complementing magnetic field paleo-intensity measurements as data sources that constrain models based on secular cooling of the Earth.

187Os-186Os and He Isotope Systematics of Iceland Picrites

NASA Astrophysics Data System (ADS)

Brandon, A. D.; Brandon, A. D.; Graham, D.; Gautason, B.

2001-12-01

Iceland is one of the longest-lived modern plumes, and seismic imaging supports a model where the roots of this plume are at the base of the lower mantle. Hence, Os isotopic data for lavas from this plume are ideal for further testing the role of core-mantle chemical exchange at the site of plume generation in the lower mantle, and for addressing the origin of Os-He isotopic variation in plumes. Recent work has shown that lavas from some plume systems (Hawaii, Noril'sk-Siberia, Gorgona) show coupled enrichments in 186Os/188Os and 187Os/188Os, not observed in upper mantle materials including abyssal peridotites. Picrites from Hawaii display a positive correlation between 186Os/188Os and He isotopes (R/Ra), where range in 186Os/188Os of 0.119834+/-28 to 0.1198475+/-29 and corresponding R/Ra from +7 to +25. These systematics are consistent with a lower mantle source for the radiogenic 186Os signal in the Hawaiian plume. The coupled Os enrichments in these plumes has been attributed to core-mantle chemical exchange, consistent with generation of the Hawaiian plume at the base of the lower mantle in D". Other potentially viable models await additional scrutiny. New He isotope and high precision 186Os/188Os and 187Os/188Os measurements for Iceland picrites show unique systematics compared to Hawaii. These picrites have 187Os/188Os ranging from 0.1297 to 0.1381 and R/Ra of +9 to +18, with generally higher R/Ra correlating with higher 187Os/188Os. Unlike the Hawaiian picrites from Hualalai and Loihi, which have coupled enrichments in 186Os/188Os and 187Os/188Os, the Iceland picrites show no enrichment 186Os/188Os - 0.1198363+/-28 (2s, n=14). Such Os-He isotopic variations require one end-member source that has high R/Ra, coupled with a long term elevated Re/Os and Pt/Os similar to that of the upper mantle. These systematics are inconsistent with either known upper mantle materials or those purported for ancient recycled slabs and may be a previously unidentified component in the lower mantle.

The Central Atlantic Magmatic Province (CAMP)

NASA Astrophysics Data System (ADS)

Marzoli, A.; Callegaro, S.; Davies, J.; Chiaradia, M.; Reisberg, L. C.; Merle, R.; Jourdan, F.; Bertrand, H.; Youbi, N.

2017-12-01

Basaltic lava flows, dykes, sills, and layered intrusion of the CAMP (Central Atlantic magmatic province) crop out in Europe, Africa, North and South America over > 10 million square km, making this one of Earth's largest igneous provinces. CAMP is characterized by 100-400 m thick preserved lava piles and by huge shallow intrusions (e.g., > 1.5 million cubic km sills). Magmatism occurred mainly between 201.6 and 201.1 Ma (according to U-Pb and Ar/Ar ages) during the end-Triassic extinction event and a few Ma before break-up of Pangea. Pulsed emplacement seems consistent with high-precision geochronology, but needs further confirmation. All over the province, basalts with quite similar composition reflect a common mantle source. These basalts have low Ti contents (TiO2 ca. 1.0-1.3 wt.%), moderately enriched Sr-Nd-Pb isotopic compositions close to the EM-II mantle end-member, and 187Os/188Os close to 0.130. We attribute these characteristics to a dominant shallow asthenospheric mantle source that was enriched by subduction-related components. Assimilation of crustal rocks generally played a minor role and rarely exceed 5-10%. Instead, assimilation of the sub-continental lithospheric mantle (SCLM) was instead recognized in the high-Ti basalts (TiO2> 2.0 wt.%) that were emplaced in a restricted area around the Man and Amazonian cratons (Sierra Leone, Liberia, Brazil, Guyana). The SCLM-like signature of these basalts suggests assimilation of metasomatically enriched parts of the SCLM. Also early basalts emplaced north of the West African craton (Morocco, Mali) are contaminated by enriched SCLM components even if to a lesser degree, while later basalts from the same African regions have low 187Os/188Os (ca. 0.120) and probably tapped a more depleted cratonic SCLM. Calculated mantle potential temperatures are low (ca. 1450 °C) and geochemical data do not support a significant contribution from mantle-plume material. The only available He isotopic data are just slightly higher than those of MORB. This argues against a substantial contribution from mantle-plume material. The only basalts trending to isotopic compositions similar to those of present-day Atlantic island basalts are quite limited in volume and restricted to a small area of Morocco.

Subduction-modified oceanic crust in the sources of continental picrite dikes from the Karoo LIP?

NASA Astrophysics Data System (ADS)

Heinonen, J. S.; Carlson, R. W.; Riley, T. R.; Luttinen, A. V.; Horan, M. F.

2013-12-01

The Ahlmannryggen mountain range in East Antarctica hosts unusual LILE-depleted, but Fe- and Ti-enriched ultramafic dikes (Group 3) that belong to the Jurassic (~180 Ma) Karoo continental flood basalt (CFB) province. Their high initial ɛNd (+5 to +9) indicates their origin within the sublithospheric mantle beneath the Gondwana supercontinent. Using the new Pb and Os isotopic data and previously published geochemical and mineral chemical data, we try to constrain their mantle sources. The dikes that lack evidence of crustal contamination exhibit very radiogenic ɛNd (+8.6 to +9.0), relatively radiogenic 206Pb/204Pb (18.2-18.4) and 87Sr/86Sr (0.7035-0.7037), and unradiogenic 187Os/188Os (0.124-0.125) at 180 Ma. These isotopic compositions are unlike those typical of MORBs, excluding depleted mantle as the sole source contributor. The Pb isotopic composition of the dikes plots close to the 4.43 Ga geochron and hence is compatible with derivation from an early-depleted reservoir (EDR), recently suggested to be a major source component in CFBs. However, the high ɛNd of the dikes exceeds the ɛNd estimated for EDR (+4.9 to +8.5 at 180 Ma) and the relative Nb, Fe, and Ti enrichment (pyroxenite fingerprint) of the dikes is not readily ascribed to EDR source. Based on our isotopic and trace element modeling, we regard that the mantle source of the picrite dikes contained seawater-altered and subduction-modified MORB with a recycling age of 0.8 Ga. Such a source component would explain the unusual combination of elevated initial 87Sr/86Sr, ɛNd, and 206Pb/204Pb, relative depletion in fluid-mobile LILE, U, Th, Pb, and LREE, and relative enrichment in Nb, Fe, Ti, and other HFSE. Behavior of Re and Os in subduction environments is not well constrained, but loss of Re from recycled MORB, as observed in some subduction-associated eclogites and blueschists, and predominant contribution of Os from depleted peridotite matrix could have produced the observed low 187Os/188Os. Pyroxenite sources also are consistent with mineral chemical data (e.g., high-Ni olivine) for the picrite dikes. Such peculiar sources were likely not a predominant component in Karoo magmatism in general. Nevertheless, less subduction-modified or more enriched (e.g., additional sediment component) recycled crustal signatures would be difficult to distinguish from the 'lithospheric signatures' of many common CFBs. In addition to depleted mantle or EDR components that have been identified in the high-Mg dikes of the adjacent Vestfjella mountain range, a variety of recycled source components could thus be hiding in the geochemical jungle of the Karoo (and other) CFBs.

Isotope and trace element insights into heterogeneity of subridge mantle

NASA Astrophysics Data System (ADS)

Mallick, Soumen; Dick, Henry J. B.; Sachi-Kocher, Afi; Salters, Vincent J. M.

2014-06-01

Geochemical data for abyssal peridotites are used to determine the relationship to mid-ocean ridge basalts from several locations at ridge segments on the SW Indian Ridge (SWIR), the Mid-Cayman-Rise (MCR), and the Mid-Atlantic Ridge (MAR). Based on chemical and petrological criteria peridotites are categorized as being either dominantly impregnated with melt or being residual after recent melting. Those that are considered impregnated with melt also have isotopic compositions similar to the basalts indicating impregnation by an aggregate MORB melt. A SWIR and MCR residual peridotite Nd-isotopic compositions partly overlap the Nd-isotopic compositions of the basalts but extend to more radiogenic compositions. The differences between peridotite and basalt Nd-isotopic compositions can be explained by incorporating a low-solidus component with enriched isotopic signature in the subridge mantle: a component that is preferentially sampled by the basalts. At the MAR, peridotites and associated basalts have overlapping Nd-isotopic compositions, suggesting a more homogeneous MORB mantle. The combined chemistry and petrography indicates a complex history with several depletion and enrichment events. The MCR data indicate that a low-solidus component can be a ubiquitous component of the asthenosphere. Residual abyssal peridotites from limited geographic areas also show significant chemical variations that could be associated with initial mantle heterogeneities related to events predating the ridge-melting event. Sm-Nd model ages for possible earlier depletion events suggest these could be as old as 2.4 Ga. This article was corrected on 9 JULY 2014. See the end of the full text for details.

The Mantle Isotopic Array: A Tale of Two FOZOs

NASA Astrophysics Data System (ADS)

Apen, F. E.; Mukhopadhyay, S.; Williams, C. D.

2017-12-01

Oceanic basalts display isotopic arrays that suggest mixing between a depleted component, several enriched components, and a primitive component. The topology of the arrays provides information on mantle mixing, the distribution of heterogeneities, and information on mantle structure. Here we use a global compilation of mid-ocean ridge basalt (MORB) and ocean island basalt (OIB) He-Sr-Nd-Pb isotopic data to further analyze the topology of these arrays. Previous work indicated that OIB isotopic arrays converge to a common component [1-3] referred to as the focus zone, or FOZO. Our analyses suggest that while all OIBs do point to a common component with unradiogenic 4He/3He ratios relative to MORBs, this component has to be quite variable in its He, Sr, Nd and Pb isotopic compositions. FOZO cannot be a pure component but must represent a heterogeneous mixture of primitive and recycled material. Our analyses of the MORB and OIB isotopic compositions also indicate that while MORBs and OIBs sample the same components, the topology of their mixing arrays are quite distinct. Different MOR segments show quasi-linear isotopic arrays that all converge to a common component. This component is distinctive from the OIB FOZO being more depleted and more restrictive in its He, Sr, Nd and Pb composition. We suggest two common but distinguishable components are present in the mantle arrays: one common to MORBs and the other to OIBs, and we refer to them as MORB-FOZO and OIB-FOZO, respectively. We interpret the two FOZOs to represent the average composition of small-scale heterogeneities that make up the background matrix in the sources of MORBs and OIBs. The depleted and enriched components that are sampled in MORBs and OIBs reflect relatively large-scale heterogeneities distributed within the matrix, material that have yet to be deformed into the smaller length scales of the matrix material. Differences between the two FOZO compositions reflects the inclusion of a component with primitive He in OIBs along with differences in mixing timescales and mantle processing rates for MORBs and OIBs. The two distinct FOZO compositions must also indicate limited direct mixing between the two over Earth's 4.5 Gyr history. References: [1] Hart et al., Science 1992; [2] Farley et al., EPSL 1992; [3] Hanan and Graham, Science 1996.

Pb evolution in the Martian mantle

NASA Astrophysics Data System (ADS)

Bellucci, J. J.; Nemchin, A. A.; Whitehouse, M. J.; Snape, J. F.; Bland, P.; Benedix, G. K.; Roszjar, J.

2018-03-01

The initial Pb compositions of one enriched shergottite, one intermediate shergottite, two depleted shergottites, and Nakhla have been measured by Secondary Ion Mass Spectrometry (SIMS). These values, in addition to data from previous studies using an identical analytical method performed on three enriched shergottites, ALH 84001, and Chassigny, are used to construct a unified and internally consistent model for the differentiation history of the Martian mantle and crystallization ages for Martian meteorites. The differentiation history of the shergottites and Nakhla/Chassigny are fundamentally different, which is in agreement with short-lived radiogenic isotope systematics. The initial Pb compositions of Nakhla/Chassigny are best explained by the late addition of a Pb-enriched component with a primitive, non-radiogenic composition. In contrast, the Pb isotopic compositions of the shergottite group indicate a relatively simple evolutionary history of the Martian mantle that can be modeled based on recent results from the Sm-Nd system. The shergottites have been linked to a single mantle differentiation event at 4504 Ma. Thus, the shergottite Pb isotopic model here reflects a two-stage history 1) pre-silicate differentiation (4504 Ma) and 2) post-silicate differentiation to the age of eruption (as determined by concordant radiogenic isochron ages). The μ-values (238U/204Pb) obtained for these two different stages of Pb growth are μ1 of 1.8 and a range of μ2 from 1.4-4.7, respectively. The μ1-value of 1.8 is in broad agreement with enstatite and ordinary chondrites and that proposed for proto Earth, suggesting this is the initial μ-value for inner Solar System bodies. When plotted against other source radiogenic isotopic variables (Sri, γ187Os, ε143Nd, and ε176Hf), the second stage mantle evolution range in observed mantle μ-values display excellent linear correlations (r2 > 0.85) and represent a spectrum of Martian mantle mixing-end members (depleted, intermediate, enriched).

Solar helium and neon in the Earth

NASA Technical Reports Server (NTRS)

Honda, M.; Mcdougall, I.; Patterson, D. B.

1994-01-01

Neon isotopic compositions in mantle-derived samples commonly are enriched in (20)Ne and (21)Ne relative to (22)Ne compared with atmospheric neon ((20)Ne/(22)Ne and (21)Ne/(22)Ne ratios in atmospheric neon are 9.8 and 0.029, respectively), together with significant primordial (3)He. Such results have been obtained on MORB's, intraplate plume-related oceanic island basalts, backarc basin basalts, mantle xenoliths, ancient diamonds and CO2 well gases (e.g., 1 - 8). The highest (20)Ne/(22)Ne ratio observed in MORB glasses (= 13.6 plus or minus 1.3 is close to the solar value (= 13.6, as observed in solar wind). In order to explain the enrichment of (20)Ne and (21)Ne relative to atmospheric neon for samples derived from the mantle, it is necessary to postulate the presence of at least two distinct non-atmospheric components. The two most likely candidates are solar and nucleogenic ((20)Ne/(22)Ne solar = 13.6 (21)Ne/(22)Ne solar = 0.032, (20)Ne/(22)Ne nucleogenic = 2.5 and (21)Ne/(22)Ne nucleogenic = 32). This is because solar neon is the only known component with a (20)Ne/(22)Ne ratio greater than both the atmospheric value and that observed in samples derived from the mantle. Nucleogenic neon is well known to elevate (21)Ne/(22)Ne ratios. Neon isotopic signatures observed in mantle-derived samples can be accounted for by mixing of the three neon end members: solar, nucleogenic and atmospheric.

Using mineral geochemistry to decipher slab, mantle, and crustal input in the generation of high-Mg andesites and basaltic andesites from the northern Cascade Arc

USGS Publications Warehouse

Sas, May; DeBari, Susan; Clynne, Michael A.; Rusk, Brian G.

2017-01-01

To better understand the role of slab melt in the petrogenesis of North Cascades magmas, this study focuses on petrogenesis of high-Mg lavas from the two northernmost active volcanoes in Washington. High-Mg andesites (HMA) and basaltic andesites (HMBA) in the Cascade Arc have high Mg# [molar Mg/(Mg+Fe2+)] relative to their SiO2 contents, elevated Nd/Yb, and are Ni- and Cr-enriched. The rock units examined here include the Tarn Plateau HMBA (51.8–54.0 wt% SiO2, Mg# 68–70) and Glacier Creek HMA (58.3–58.7 wt% SiO2, Mg# 63–64) from the Mount Baker Volcanic Field, and the Lightning Creek HMBA (54.8–54.6 SiO2, Mg# 69–73) from Glacier Peak. This study combines major and trace element compositions of minerals and whole rocks to test several petrogenetic hypotheses and to determine which, if any, are applicable to North Cascades HMA and HMBA. In the Tarn Plateau HMBA, rare earth element (REE) equilibrium liquids calculated from clinopyroxene compositions have high Nd/Yb that positively correlates with Mg#. This correlation suggests an origin similar to that proposed for Aleutian adakites, where intermediate, high Nd/Yb slab-derived melts interact with the overlying mantle to become Mg-rich, and subsequently mix with low Nd/Yb, mantle-derived mafic magmas with lower Mg#. In the Glacier Creek HMA, elevated whole-rock MgO and SiO2 contents resulted from accumulation of xenocrystic olivine and differentiation processes, respectively, but the cause of high Nd/Yb is less clear. However, high whole-rock Sr/P (fluid mobile/fluid immobile) values indicate a mantle source that was fluxed by an enriched, hydrous slab component, likely producing the observed high Nd/Yb REE signature. The Lightning Creek HMBA is a hybridized rock unit with at least three identifiable magmatic components, but only one of which has HMA characteristics. Cr and Mg contents in Cr-spinel and olivine pairs in this HMA component suggest that its source is a strongly depleted mantle, and high whole-rock Sr/P values indicate mantle melting that was induced through hydration, likely adding the component responsible for the observed high Nd/Yb REE pattern. The elevated SiO2 contents (54.6 wt%) of the HMA component resulted from differentiation or high degrees of partial melting of ultramafic material through the addition of H2O. Therefore the Lightning Creek HMBA is interpreted to have originated from a refractory mantle source that underwent melting through interaction with an enriched slab component. Our results indicate that in addition to slab-derived fluids, slab-derived melts also have an important role in the production of HMA and HMBA in the north Cascade Arc.

Mantle Sulfur Cycle: A Case for Non-Steady State ?

NASA Astrophysics Data System (ADS)

Cartigny, Pierre; Labidi, Jabrane

2016-04-01

Data published over the last 5 years show that the early inference that mantle is isotopically homogeneous is no more valid. Instead, new generation data on lavas range over a significant 34S/32S variability of up to 5‰ with δ 34S values often correlated to Sr- and Nd-isotope compositions. This new set of data also reveals the Earth's mantle to have a sub-chondritic 34S/32S ratio, by about ˜ 1‰. We will present at the conference our published and unpublished data on samples characterizing the different mantle components (i.e. EM1, EM2, HIMU and LOMU). All illustrate 34S-enrichments compared to MORB with Δ 33S and Δ 36S values indistinguishable from CDT or chondrites at the 0.03‰ level. These data are consistent with the recycling of subducted components carrying sulfur with Δ 33S and Δ 36S-values close to zero. Archean rocks commonly display Δ 33S and Δ 36S values deviating from zero by 1 to 10 ‰. The lack of variations for Δ 33S and Δ 36S values in present day lava argue against the sampling of any subducted protolith of Archean age in their mantle source. Instead, our data are consistent with the occurrence of Proterozoic subducted sulfur in the source of the EM1, EM2, LOMU and HIMU endmember at the St-Helena island. This is in agreement with the age of those components early derived through the use of the Pb isotope systematic. Currently, the negative δ 34S-values of the depleted mantle seem to be associated with mostly positive values of enriched components. This would be inconsistent with the concept a steady state of sulfur. Assuming that the overall observations of recycled sulfur are not biased, the origin of such a non-steady state remains unclear. It could be related to the relatively compatible behavior of sulfur during partial melting, as the residue of present-day melting can be shown to always contain significant amounts of sulfide (50{%} of what is observed in a fertile source). This typical behavior likely prevents an efficient extraction of mantle S over time, hence inhibiting quantitative mixing between surface and mantle S. This also allows the preservation of any primitive signature of the deep sulfur cycle to be potentially recorded.

Large volume recycling of oceanic lithosphere over short time scales: geochemical constraints from the Caribbean Large Igneous Province

NASA Astrophysics Data System (ADS)

Hauff, F.; Hoernle, K.; Tilton, G.; Graham, D. W.; Kerr, A. C.

2000-01-01

Oceanic flood basalts are poorly understood, short-term expressions of highly increased heat flux and mass flow within the convecting mantle. The uniqueness of the Caribbean Large Igneous Province (CLIP, 92-74 Ma) with respect to other Cretaceous oceanic plateaus is its extensive sub-aerial exposures, providing an excellent basis to investigate the temporal and compositional relationships within a starting plume head. We present major element, trace element and initial Sr-Nd-Pb isotope composition of 40 extrusive rocks from the Caribbean Plateau, including onland sections in Costa Rica, Colombia and Curaçao as well as DSDP Sites in the Central Caribbean. Even though the lavas were erupted over an area of ˜3×10 6 km 2, the majority have strikingly uniform incompatible element patterns (La/Yb=0.96±0.16, n=64 out of 79 samples, 2σ) and initial Nd-Pb isotopic compositions (e.g. 143Nd/ 144Nd in=0.51291±3, ɛNdi=7.3±0.6, 206Pb/ 204Pb in=18.86±0.12, n=54 out of 66, 2σ). Lavas with endmember compositions have only been sampled at the DSDP Sites, Gorgona Island (Colombia) and the 65-60 Ma accreted Quepos and Osa igneous complexes (Costa Rica) of the subsequent hotspot track. Despite the relatively uniform composition of most lavas, linear correlations exist between isotope ratios and between isotope and highly incompatible trace element ratios. The Sr-Nd-Pb isotope and trace element signatures of the chemically enriched lavas are compatible with derivation from recycled oceanic crust, while the depleted lavas are derived from a highly residual source. This source could represent either oceanic lithospheric mantle left after ocean crust formation or gabbros with interlayered ultramafic cumulates of the lower oceanic crust. High 3He/ 4He in olivines of enriched picrites at Quepos are ˜12 times higher than the atmospheric ratio suggesting that the enriched component may have once resided in the lower mantle. Evaluation of the Sm-Nd and U-Pb isotope systematics on isochron diagrams suggests that the age of separation of enriched and depleted components from the depleted MORB source mantle could have been ≤500 Ma before CLIP formation and interpreted to reflect the recycling time of the CLIP source. Mantle plume heads may provide a mechanism for transporting large volumes of possibly young recycled oceanic lithosphere residing in the lower mantle back into the shallow MORB source mantle.

Evidence for lateral mantle plume flow feeding the Central Indian Ridge

NASA Astrophysics Data System (ADS)

Murton, B. J.; Tindle, A. G.

2003-04-01

The Central Indian Ridge exhibits morphological and geochemical features indicating lateral flow of shallow plume asthenosphere from the Reunion hot-spot to the ridge axis. South of the Marie Celeste fracture zone, at 18.25°S, the Central Indian Ridge is bound by a southward closing, “V”-shaped region of shallow crust that extends for over 800 km. Over this distance, the ridge axis deepens to the south and is also affected by left-stepping offsets that bring it towards the west. The northern end of the ridge, which is closest to the island of La'Réunion, is shallowest and dominated by an inflated segment with associated sheet flows covering over 50 square kilometres. These morphological features are usually associated with ridge-hot-spot interaction. However, the nearest active hot-spot lies over 1100 km to the west beneath the island of La'Réunion. Geochemical trends for basalts erupted along the Central Indian Ridge demonstrate a gradient of northward decreasing MgO and increasing SiO2, indicating a relationship between shallower crust and increased magmatic fractional crystallisation. Superimposed on this gradient is an excess increase in incompatible element ratios, indicative of mantle enrichment to the north. The enrichment correlates with the spreading-parallel distance between the ridge axis and the edge of the "V"-shaped region of anomalously shallow crust. Locally, the enriched mantle component is found preferentially at third-order ridge offsets and adjacent to the rift walls demonstrating melting of a compositionally stratified, spinel-lherzolite mantle. These features are evidence for shallow, lateral flow of enriched hot-spot asthenosphere at a velocity of ~333 mm yr-1 and with a flux of at least 50 m3 s-1, through a mantle 'worm', towards the ridge axis where it migrates south at a rate of 54 - 67 mm per year. The trend of the geochemical enrichment points to mixing between deeper N-MORB and shallower Reunion hot-spot sources beneath the Central Indian Ridge.

Combined Li-He isotopes in Iceland and Jan Mayen basalts and constraints on the nature of the North Atlantic mantle

NASA Astrophysics Data System (ADS)

Magna, T.; Wiechert, U.; Stuart, F. M.; Halliday, A. N.; Harrison, D.

2011-02-01

Lithium (Li) isotopes are thought to provide a powerful proxy for the recycling of crustal material, affected by low temperature alteration, through the mantle. We present Li isotope compositions for basaltic volcanic rocks from Hengill, Iceland, and Jan Mayen in order to examine possible links between ocean island volcanism and recycled oceanic crust and to address recent suggestions that mantle 3He/ 4He is also related to recycling of ancient slabs. Basaltic glasses spanning a range of chemical enrichment from the Hengill fissure system define an inverse correlation between δ 7Li (3.8-6.9‰) and 3He/ 4He (12-20 RA). The high- 3He/ 4He basalts have low δ 18O as well as excess Eu and high Nb/U, but carry no Li isotope evidence of being the product of recycling of altered slab or wedge material. In fact, there is no clear correlation between Li or He isotopes on the one hand and any of the other fingerprints of recycled slab components. The low- 3He/ 4He samples do have elevated Nb/U, Sr/Nd, positive Eu anomalies and high δ 7Li (˜6.9‰), providing evidence of a cumulate-enriched source that could be part of an ancient altered ocean floor slab. Basalts from Jan Mayen are characterized by large degrees of enrichment in incompatible trace elements typical of EM-like basalts but have homogeneous δ 7Li typical of depleted mantle (3.9-4.7‰) providing evidence for a third mantle source in the North Atlantic. It appears that oceanic basalts can display a wide range in isotope and trace element compositions associated with recycled components whilst exhibiting no sign of modern surface-altered slab or wedge material from the Li isotope composition.

Heterogeneous source components of intraplate basalts from NE China induced by the ongoing Pacific slab subduction

NASA Astrophysics Data System (ADS)

Chen, Huan; Xia, Qun-Ke; Ingrin, Jannick; Deloule, Etienne

2016-04-01

In recent few years, the recycled oceanic slab has been increasingly suggested to be the enriched component in the mantle source of widespread intra-plate small-volume basaltic magmatism in eastern China. The recycled oceanic slab is a mixture of sediment, upper oceanic crust and lower gabbro oceanic crust, and will undergo alteration and dehydration during the recycling progress. The influence of these different components on the mantle source needs to be further constrained. The Chaihe-aershan volcanic field in Northeast China is located close to the surface position of the front edge of the subducted Pacific slab and includes more than 35 small-volume Quaternary basaltic volcanoes, which provides an opportunity to study the evolution of mantle source in detail and the small-scale geochemical heterogeneity of the mantle source. We measured the oxygen isotopes and water content of clinopyroxene (cpx) phenocrysts by secondary ion mass spectrometry (SIMS) and Fourier transform infrared spectrometry (FTIR), respectively. The water content of magma was then estimated based on the partition coefficient of H2O between cpx and basaltic melt. The measured δ18O of cpx phenocrysts (4.27 to 8.57) and the calculated H2O content of magmas (0.23-2.70 wt.%) show large variations, reflecting the compositional heterogeneity of the mantle source. The δ18O values within individual samples also display a considerable variation, from 1.28 to 2.31‰ suggesting mixing of magmas or the sustained injection of magmas with different δ18O values during the crystallization. The relationship between the averaged δ18O values of cpx phenocrysts and the H2O/Ce, Ba/Th, Nb/La ratios and Eu anomaly of whole-rocks demonstrates the contribution to three components in the mantle source (hydrothermally altered upper oceanic crust or marine sediments, altered lower gabbroic oceanic crust, ambient mantle). The proportions of these three components varied strongly within a limited period (˜1.27 Ma to ˜0.25 Ma). As only the Pacific slab is constantly subducted to the eastern Asia during that time, we suggested that its ongoing subduction is the only reasonable candidate to result in the compositional heterogeneity and rapid variation of enriched components in such a limited and recent time. Combines with previous studies on other basalt localities of eastern China, these new results confirm that the Pacific slab subduction play a key role in the triggering of the wide spread Cenozoic basaltic volcanism in eastern China.

Contrasting geochemical trends in the fertile and refractory parts of the NE Atlantic mantle source

NASA Astrophysics Data System (ADS)

Tronnes, R. G.; Debaille, V.; Brandon, A. D.; Waight, T. E.; Graham, D. W.; Williams, A.; Lee, C. A.

2008-12-01

Primitive alkaline basalts from the Icelandic off-rift volcanic zones and Jan Mayen represent low-degree melts from the fertile parts of the NE Atlantic mantle. Olivine tholeiites and picrites from the Icelandic rift zones and nearby oceanic spreading ridges are formed by protracted decompressional melting. The V-shaped ridges along the Reykjanes, Kolbeinsey and Aegir ridges indicate that ascending source material is supplied by a pulsating plume and deflected laterally for distances of about 1000 km from Iceland (Jones et al. GGG 2002; Breivik et al. JGR 2006). Plume material deflected in the direction of the rift zones and spreading ridges undergoes extensive melting at shallow level, whereas material deflected in other directions flows laterally at deeper levels and remains largely unmelted and more fertile. The comparison of a sample suite of primitive off-rift basalts from Iceland and Jan Mayen (Debaille et al., in prep.) with olivine tholeiites and picrites from the Icelandic rift zones (mainly Brandon et al. GCA 2007) demonstrate opposing geochemical trends. The degree of source enrichment, expressed by the La/Sm-ratio, is positively and negatively correlated with 87/86Sr and 143/144Nd throughout the entire range of depleted rift zone tholeiites and enriched off-rift basalts. In the rift zone tholeiites the La/Sm-ratio has negative correlations with Mg# and Mg-content and positive correlations with 187/188Os and 3/4He. These four trends have opposite equivalents for the off-rift basalts. The most enriched and alkaline basalts from Jan Mayen and Snæfellsnes have the lowest 3/4He of 6-9*Ra and 187/188Os of 0.12-0.13. The trends seem to require a source component with ancient melt depletion and subsequent enrichment. A subcontinental lithospheric mantle keel (SCLM) is the most likely origin for the enriched component with high LILE, La/Sm and 87/86Sr and low 143/144Nd, 3/4He and 187/188Os. The most enriched alkaline basalts have notably higher Mg# and Mg and lower Fe and Na (but higher Ti, K and P) than the least enriched off-rift basalts. The first order geochemical variation in the off-rift basalts can be modelled by progressive partial melting of a pseudo-binary source mixture of the SCLM- component and a composite component with high 143/144Nd and 3/4He and low 87/86Sr. Depleted MORB- like asthenosphere is required to model the further progressive melting of the rift-related tholeiitic basalts.

Zircon Hf-O isotopic constraints on the origin of Late Mesozoic felsic volcanic rocks from the Great Xing'an Range, NE China

NASA Astrophysics Data System (ADS)

Gong, Mingyue; Tian, Wei; Fu, Bin; Wang, Shuangyue; Dong, Jinlong

2018-05-01

The voluminous Late Mesozoic magmatism was related to extensive re-melting of juvenile materials that were added to the Central East Asia continent in Phanerozoic time. The most favoured magma generation mechanism of Late Mesozoic magmas is partial melting of underplated lower crust that had radiogenic Hf-Nd isotopic characteristics, but this mechanism faces difficulties when interpreting other isotopic data. The tectonic environment controlling the generation of the Late Mesozoic felsic magmas is also in dispute. In this study, we obtained new U-Pb ages, and geochemical and isotopic data of representative Jurassic (154.4 ± 1.5 Ma) and Cretaceous (140.2 ± 1.5 Ma) felsic volcanic samples. The Jurassic sample has inherited zircon cores of Permian age, with depleted mantle-like εHf(t) of +7.4 - +8.5, which is in contrast with those of the magmatic zircons (εHf(t) = +2.4 ± 0.7). Whereas the inherited cores and the magmatic zircons have identical mantle-like δ18O composition ranges (4.25-5.29‰ and 4.69-5.54‰, respectively). These Hf-O isotopic characteristics suggest a mixed source of enriched mantle materials rather than ancient crustal components and a depleted mantle source represented by the inherited Permian zircon core. This mechanism is manifested by the eruption of Jurassic alkaline basalts originated from an enriched mantle source. The Cretaceous sample has high εHf(t) of +7.0 - +10.5, suggesting re-melting of a mafic magma derived from a depleted mantle-source. However, the sub-mantle zircon δ18O values (3.70-4.58‰) suggest the depleted mantle-derived mafic source rocks had experienced high temperature hydrothermal alteration at upper crustal level. Therefore, the Cretaceous felsic magma, if not all, could be generated by re-melting of down-dropped supracrustal volcanic rocks that experienced high temperature oxygen isotope alteration. The two processes, enriched mantle-contribution and supracrustal juvenile material re-melting, are new generation mechanisms of the Late Mesozoic magmas from Central East Asia. Rift settings may have controlled these processes throughout crustal and mantle levels.

South-to-north pyroxenite-peridotite source variation correlated with an OIB-type to arc-type enrichment of magmas from the Payenia backarc of the Andean Southern Volcanic Zone (SVZ)

NASA Astrophysics Data System (ADS)

Brandt, Frederik Ejvang; Holm, Paul Martin; Søager, Nina

2017-01-01

New high-precision minor element analysis of the most magnesian olivine cores (Fo85-88) in fifteen high-MgO (Mg#66-74) alkali basalts or trachybasalts from the Quaternary backarc volcanic province, Payenia, of the Andean Southern Volcanic Zone in Argentina displays a clear north-to-south decrease in Mn/Feol. This is interpreted as the transition from mainly peridotite-derived melts in the north to mainly pyroxenite-derived melts in the south. The peridotite-pyroxenite source variation correlates with a transition of rock compositions from arc-type to OIB-type trace element signatures, where samples from the central part of the province are intermediate. The southernmost rocks have, e.g., relatively low La/Nb, Th/Nb and Th/La ratios as well as high Nb/U, Ce/Pb, Ba/Th and Eu/Eu* = 1.08. The northern samples are characterized by the opposite and have Eu/Eu* down to 0.86. Several incompatible trace element ratios in the rocks correlate with Mn/Feol and also reflect mixing of two geochemically distinct mantle sources. The peridotite melt end-member carries an arc signature that cannot solely be explained by fluid enrichment since these melts have relatively low Eu/Eu*, Ba/Th and high Th/La ratios, which suggest a component of upper continental crust (UCC) in the metasomatizing agent of the northern mantle. However, the addition to the mantle source of crustal materials or varying oxidation state cannot explain the variation in Mn and Mn/Fe of the melts and olivines along Payenia. Instead, the correlation between Mn/Feol and whole-rock (wr) trace element compositions is evidence of two-component mixing of melts derived from peridotite mantle source enriched by slab fluids and UCC melts and a pyroxenite mantle source with an EM1-type trace element signature. Very low Ca/Fe ratios ( 1.1) in the olivines of the peridotite melt component and lower calculated partition coefficients for Ca in olivine for these samples are suggested to be caused by higher H2O contents in the magmas derived from subduction zone enriched mantle. Well-correlated Mn/Fe ratios in the wr and primitive olivines demonstrate that the Mn/Fewr of these basalts that only fractionated olivine and chromite reflects the Mn/Fe of the primitive melts and can be used as a proxy for the amount of pyroxenite melt in the magmas. Using Mn/Fewr for a large dataset of primitive Payenia rocks, we show that decreasing Mn/Fewr is correlated with decreasing Mn and increasing Zn/Mn as expected for pyroxenite melts.

Geodynamic control on melt production in the central Azores : new insights from major and trace elements, Sr, Nd, Pb, Hf isotopic data and K/Ar ages on the islands of Terceira, Sao Jorge and Faial

NASA Astrophysics Data System (ADS)

Hildenbrand, A.; Weis, D. A.; Madureira, P.; Marques, F. O.

2012-12-01

A combined geochronological and geochemical study has been carried out on the volcanic islands of Terceira, São Jorge, and Faial (central Azores) to examine the relationships between mantle dynamics, melt production and regional deformation close to the triple junction between the American, the Eurasian and the Nubian lithospheric plates. The lavas analyzed span the last 1.3 Myr, and have been erupted during two main periods prior to 800 ka and after 750 ka, respectively. They range in composition from alkaline basalts/basanites to trachytes, and overall exhibit a strong enrichment in highly incompatible elements. The whole range of isotopic compositions here reported (87Sr/86Sr: 0.703508-0.703913; 143Nd/144Nd: 0.512882-0.513010; 206Pb/204Pb: 19.0840- 20.0932; 207Pb/204Pb: 15.5388-15.6409; 208Pb/204Pb: 38.7416-39.3921; 176Hf/177Hf: 0.282956-0.283111) suggests the involvement of three components: (1) a weakly radiogenic component reflecting the source of regional MORBs, (2) a main HIMU-type component represented in the three islands, and (3) an additional component in Faial recent lavas, which appears similar to the EM type end-member previously recognized on other Azores eruptive complexes. The geographical distribution of the enriched components and the synchronous construction of various islands at the regional scale rules out a single narrow active plume. They suggest in turn the presence of dispersed residual enriched mantle blobs, interpreted as remnants from a large heterogeneous plume probably responsible for edification of the Azores plateau several Myr ago. The lavas erupted in São Jorge and Faial prior to 800 ka have similar and homogeneous isotopic ratios, which partly overlap the compositional field of MORBs from the adjacent portion of the Mid-Atlantic Ridge (MAR). Their genesis can be explained by the regional development of N150 transtensive tectonic structures, which promoted significant decompression melting of the upper mantle, with correlative dilute expression of the enriched components. In contrast, the youngest lavas (< 750 ka) erupted along the N110 main structural direction on the three islands are significantly enriched in LILE and LREE, and generally have variable but more radiogenic isotopic compositions. Such characteristics suggest low-degree partial melting and greater incorporation of fertile residual mantle anomalies during passive tectonic reactivation of pre-existing transform faults promoted by recent ridge-push at the MAR. We propose that sub-aerial volcanism over the last 1.3 Myr in the central Azores recorded a sudden change in the conditions of melt generation which most probably reveals a major reconfiguration of regional deformation accompanying the recent geodynamic reorganization of the Eurasia-Nubia plate boundary.

Geology, geochronology, and geochemistry of basaltic flows of the Cat Hills, Cat Mesa, Wind Mesa, Cerro Verde, and Mesita Negra, central New Mexico

USGS Publications Warehouse

Maldonado, F.; Budahn, J.R.; Peters, L.; Unruh, D.M.

2006-01-01

The geochronology, geochemistry, and isotopic compositions of basaltic flows erupted from the Cat Hills, Cat Mesa, Wind Mesa, Cerro Verde, and Mesita Negra volcanic centres in central New Mexico indicate that each of these lavas had unique origins and that the predominant mantle involved in their production was an ocean-island basalt type. The basalts from Cat Hills (0.11 Ma) and Cat Mesa (3.0 Ma) are similar in major and trace element composition, but differences in MgO contents and Pb isotopic values are attributed to a small involvement of a lower crustal component in the genesis of the Cat Mesa rocks. The Cerro Verde rock is comparable in age (0.32 Ma) to the Cat Hills lavas, but it is more radiogenic in Sr and Nd, has higher MgO contents, and has a lower La/Yb ratio. This composition is explained by the melting of an enriched mantle source, but the involvement of another crustal component cannot be disregarded. The Wind Mesa rock is characterized by similar age (4.01 Ma) and MgO contents, but it has enriched rare-earth element contents compared with the Cat Mesa samples. These are attributed to a difference in the degree of partial melting of the Cat Mesa source. The Mesita Negra rock (8.11 Ma) has distinctive geochemical and isotopic compositions that suggest a different enriched mantle and that large amounts of a crustal component were involved in generating this magma. These data imply a temporal shift in magma source regions and crustal involvement, and have been previously proposed for Rio Grande rift lavas. ?? 2006 NRC Canada.

Dynamical consequences of mantle heterogeneity in two-phase models of mid-ocean ridges

NASA Astrophysics Data System (ADS)

Katz, R. F.

2010-12-01

The mid-ocean ridge system, over 50,000 km in length, samples the magmatic products of a large swath of the asthenosphere. It provides our best means to assess the heterogeneity structure of the upper mantle. Interpretation of the diverse array of observations of MOR petrology, geochemistry, tomography, etc requires models that can map heterogeneity structure onto predictions testable by comparison with these observations. I report on progress to this end; in particular, I describe numerical models of coupled magma/mantle dynamics at mid-ocean ridges [1,2]. These models incorporate heterogeneity in terms of a simple, two-component thermochemical system with specified amplitude and spatial distribution. They indicate that mantle heterogeneity has significant fluid-dynamical consequences for both mantle and magmatic flow. Models show that the distribution of enrichment can lead to asymmetry in the strength of upwelling across the ridge-axis and channelised magmatic transport to the axis. Furthermore, heterogeneity can cause off-axis upwelling of partially molten diapirs, trapping of enriched melts off-axis, and re-fertilization of the mantle by pooled and refrozen melts. Predicted consequences of geochemical heterogeneity may also be considered. References: [1] Katz, RF, (2008); Magma dynamics with the Enthalpy Method: Benchmark Solutions and Magmatic Focusing at Mid-ocean Ridges. Journal of Petrology, doi: 10.1093/petrology/egn058. [2] Katz RF, (2010); Porosity-driven convection and asymmetry beneath mid-ocean ridges. Submitted to G3.

Within-plate Cenozoic Volcanism and Mantle Sources Within The Western-central Mediterranean Area

NASA Astrophysics Data System (ADS)

Beccaluva, L.; Bianchini, G.; Bonadiman, C.; Coltorti, M.; Siena, F.

An integrated study of anorogenic basic magmas and entrained mantle xenoliths rep- resents a promising approach for a comprehension of the magmatogenic events occur- ring within the lithospheric mantle in the western-central Mediterranean area. In this contribution we review the geochemical characteristics of mafic lavas and associated peridotite xenoliths from three anorogenic volcanic districts: Pliocene-Quaternary vol- canism of Sardinia; Pliocene-Quaternary volcanism of the Iblean area (eastern Sicily); Paleocene-Oligocene Veneto Volcanic Province. Investigations have been focused on 1) petrological features of parental magmas, which may contribute to infer the com- positional characteristics of mantle sources and to constrain the modes of partial melt- ing; 2) modelling the depletion events and metasomatic enrichments in mantle xeno- liths of the three volcanic districts, as well as the nature of their causative agents. Petrological features and Sr-Nd-Pb isotopic data, both of lava and xenoliths, indicate that DM+HIMU components distinguish the lithospheric mantle sections of Iblean and Veneto Volcanic Provinces. On the other hand, lavas and xenoliths from Sardinia display a significant different isotopic signature characterised by DM+EM1. Similar geochemical fingerprints, i.e. the significant presence of EM components are gener- ally recorded by mafic lavas and mantle xenoliths from the European Plate, whereas they are not observed in the stable African lithospheric domain.

Transition From Archean Plume-Arc Orogens to Phanerozoic Style Convergent Margin Orogens, and Changing Mantle Lithosphere

NASA Astrophysics Data System (ADS)

Kerrich, R.; Jia, Y.; Wyman, D.

2001-12-01

Mantle plume activity was more intense in the Archean and komatiite-basalt volcanic sequences are a major component of many Archean greenstone belts. Tholeiitic basalts compositionally resemble Phanerozoic and Recent ocean plateau basalts, such as those of Ontong Java and Iceland. However, komatiite-basalt sequences are tectonically imbricated with bimodal arc lavas and associated trench turbidites. Interfingering of komatiite flows with boninite series flows, and primitive to evolved arc basalts has recently been identified in the 2.7 Ga Abitibi greenstone belt, demonstrating spatially and temporally associated plume and arc magmatism. These observations are consistent with an intra-oceanic arc migrating and capturing an ocean plateau, where the plateau jams the arc and imbricated plateau-arc crust forms a greenstone belt orogen. Melting of shallowly subducted plateau basalt crust (high Ba, Th, LREE) accounts for the areally extensive and voluminous syntectonic tonalite batholiths. In contrast, the adakite-Mg-andesite-Niobium enriched basalt association found in Archean greenstone belts and Cenozoic arcs are melts of LREE depleted MORB slab. Buoyant residue from anomalously hot mantle plume melting at > 100km rises to couple with the composite plume-arc crust to form the distinctively thick and refractory Archean continental lithospheric mantle. New geochemical data for structurally hosted ultramafic units along the N. American Cordillera, from S. California to the Yukon, show that these are obducted slices of sub-arc lithospheric mantle. Negatively fractionated HREE with high Al2O3/TiO2 ratios signify prior melt extraction, and variably enriched Th and LREE with negative Nb anomalies a subduction component in a convergent margin. A secular decrease of mantle plume activity and temperature results in plume-arc dominated geodynamics in the Archean with shallow subduction and thick CLM, whereas Phanerozoic convergent margins are dominated by arc-continent, arc-terrane, and terrane-terrane collision with steep subduction resulting in narrow belts of granitoids and obduction of lithospheric mantle.

Extreme isotopic variations in the upper mantle: evidence from Ronda

NASA Astrophysics Data System (ADS)

Reisberg, Laurie; Zindler, Alan

1986-12-01

The Ronda Ultramafic Complex in southern Spain represents a piece of the Earth's mantle which has been tectonically emplaced into the crust. Nd and Sr isotopic analyses are presented for leached, hand-picked Cr-diopside separates prepared from 15 rock and 18 river sediment samples from Ronda. These results demonstrate that within this small, contiguous body there exists the entire range of Nd isotopic compositions, and much of the range of Sr compositions, found in rocks derived from the sub-oceanic mantle. The sediment cpx samples show that the average isotopic composition of the massif becomes progressively less "depleted" moving from SW to NE along the long axis of the massif. The rock cpx samples document 143Nd/ 144Nd variations from 0.5129 to 0.5126 and 87Sr/ 86Sr variations from 0.7031 to 0.7039 within a uniform outcrop less than 10 m in extent. Thus, extreme isotopic fluctuations exist over a wide range of wavelengths. Sr and Nd isotopes are generally inversely correlated, forming a trend on a Nd-Sr diagram that sharply crosscuts that of the "mantle array". Many of the 143Nd/ 144Nd values, and all of the Sm/Nd values, from one section of the massif are lower than that SCV015SCV0 of the bulk earth, implying that this region existed, or was influenced by a component which existed, in a LREE-enriched environment for a significant period of time. Among the sediment cpxs there is a positive correlation between 143Nd/ 144Nd and 147Sm/ 144Nd. The rock cpx separates display considerably more scatter. A simple, single-stage differentiation event starting with a uniform mantle source cannot explain these results. At least one episode of mixing with a LREE-enriched component is required. If these results from Ronda are typical of the upper mantle, basalts with different isotopic compositions need not derive from spatially separated mantle sources.

Silica-enriched mantle sources of subalkaline picrite-boninite-andesite island arc magmas

NASA Astrophysics Data System (ADS)

Bénard, A.; Arculus, R. J.; Nebel, O.; Ionov, D. A.; McAlpine, S. R. B.

2017-02-01

Primary arc melts may form through fluxed or adiabatic decompression melting in the mantle wedge, or via a combination of both processes. Major limitations to our understanding of the formation of primary arc melts stem from the fact that most arc lavas are aggregated blends of individual magma batches, further modified by differentiation processes in the sub-arc mantle lithosphere and overlying crust. Primary melt generation is thus masked by these types of second-stage processes. Magma-hosted peridotites sampled as xenoliths in subduction zone magmas are possible remnants of sub-arc mantle and magma generation processes, but are rarely sampled in active arcs. Published studies have emphasised the predominantly harzburgitic lithologies with particularly high modal orthopyroxene in these xenoliths; the former characteristic reflects the refractory nature of these materials consequent to extensive melt depletion of a lherzolitic protolith whereas the latter feature requires additional explanation. Here we present major and minor element data for pristine, mantle-derived, lava-hosted spinel-bearing harzburgite and dunite xenoliths and associated primitive melts from the active Kamchatka and Bismarck arcs. We show that these peridotite suites, and other mantle xenoliths sampled in circum-Pacific arcs, are a distinctive peridotite type not found in other tectonic settings, and are melting residues from hydrous melting of silica-enriched mantle sources. We explore the ability of experimental studies allied with mantle melting parameterisations (pMELTS, Petrolog3) to reproduce the compositions of these arc peridotites, and present a protolith ('hybrid mantle wedge') composition that satisfies the available constraints. The composition of peridotite xenoliths recovered from erupted arc magmas plausibly requires their formation initially via interaction of slab-derived components with refractory mantle prior to or during the formation of primary arc melts. The liquid compositions extracted from these hybrid sources are higher in normative quartz and hypersthene (i.e., they have a more silica-saturated character) in comparison with basalts derived from prior melt-depleted asthenospheric mantle beneath ridges. These primary arc melts range from silica-rich picrite to boninite and high-Mg basaltic andesite along a residual spinel harzburgite cotectic. Silica enrichment in the mantle sources of arc-related, subalkaline picrite-boninite-andesite suites coupled with the amount of water and depth of melting, are important for the formation of medium-Fe ('calc-alkaline') andesite-dacite-rhyolite suites, key lithologies forming the continental crust.

Mineralogy and composition of the oceanic mantle

USGS Publications Warehouse

Putirka, Keith; Ryerson, F.J.; Perfit, Michael; Ridley, W. Ian

2011-01-01

The mineralogy of the oceanic basalt source region is examined by testing whether a peridotite mineralogy can yield observed whole-rock and olivine compositions from (1) the Hawaiian Islands, our type example of a mantle plume, and (2) the Siqueiros Transform, which provides primitive samples of normal mid-ocean ridge basalt. New olivine compositional data from phase 2 of the Hawaii Scientific Drilling Project (HSDP2) show that higher Ni-in-olivine at the Hawaiian Islands is due to higher temperatures (T) of melt generation and processing (by c. 300°C) related to the Hawaiian mantle plume. DNi is low at high T, so parental Hawaiian basalts are enriched in NiO. When Hawaiian (picritic) parental magmas are transported to shallow depths, olivine precipitation occurs at lower temperatures, where DNi is high, leading to high Ni-in-olivine. Similarly, variations in Mn and Fe/Mn ratios in olivines are explained by contrasts in the temperatures of magma processing. Using the most mafic rocks to delimit Siqueiros and Hawaiian Co and Ni contents in parental magmas and mantle source compositions also shows that both suites can be derived from natural peridotites, but are inconsistent with partial melting of natural pyroxenites. Whole-rock compositions at Hawaii and Siqueiros are also matched by partial melting experiments conducted on peridotite bulk compositions. Hawaiian whole-rocks have elevated FeO contents compared with Siqueiros, which can be explained if Hawaiian parental magmas are generated from peridotite at 4-5 GPa, in contrast to pressures of slightly greater than 1 GPa for melt generation at Siqueiros; these pressures are consistent with olivine thermometry, as described in an earlier paper. SiO2-enriched Koolau compositions are reproduced if high-Fe Hawaiian parental magmas re-equilibrate at 1-1·5 GPa. Peridotite partial melts from experimental studies also reproduce the CaO and Al2O3 contents of Hawaiian (and Siqueiros) whole-rocks. Hawaiian magmas have TiO2 contents, however, that are enriched compared with melts from natural peridotites and magmas derived from the Siqueiros depleted mantle, and consequently may require an enriched source. TiO2 is not the only element that is enriched relative to melts of natural peridotites. Moderately incompatible elements, such as Ti, Zr, Hf, Y, and Eu, and compatible elements, such as Yb and Lu, are all enriched at the Hawaiian Islands. Such enrichments can be explained by adding 5-10% mid-ocean ridge basalt (crust) to depleted mantle; when the major element composition of such a mixture is recast into mineral components, the result is a fertile peridotite mineralogy.

Recycling of subducted crustal components into carbonatite melts revealed by boron isotopes

NASA Astrophysics Data System (ADS)

Hulett, Samuel R. W.; Simonetti, Antonio; Rasbury, E. Troy; Hemming, N. Gary

2016-12-01

The global boron geochemical cycle is closely linked to recycling of geologic material via subduction processes that have occurred over billions of years of Earth’s history. The origin of carbonatites, unique melts derived from carbon-rich and carbonate-rich regions of the upper mantle, has been linked to a variety of mantle-related processes, including subduction and plume-lithosphere interaction. Here we present boron isotope (δ11B) compositions for carbonatites from locations worldwide that span a wide range of emplacement ages (between ~40 and ~2,600 Ma). Hence, they provide insight into the temporal evolution of their mantle sources for ~2.6 billion years of Earth’s history. Boron isotope values are highly variable and range between -8.6‰ and +5.5‰, with all of the young (<300 Ma) carbonatites characterized by more positive δ11B values (>-4.0‰), whereas most of the older carbonatite samples record lower B isotope values. Given the δ11B value for asthenospheric mantle of -7 +/- 1‰, the B isotope compositions for young carbonatites require the involvement of an enriched (crustal) component. Recycled crustal components may be sampled by carbonatite melts associated with mantle plume activity coincident with major tectonic events, and linked to past episodes of significant subduction associated with supercontinent formation.

Midcontinent rift volcanism in the Lake Superior region: Sr, Nd, and Pb isotopic evidence for a mantle plume origin

USGS Publications Warehouse

Nicholson, S.W.; Shirey, S.B.

1990-01-01

Between 1091 and 1098 Ma, most of a 15- to 20-km thickness of dominantly tholeiitic basalt erupted in the Midcontinent Rift System of the Lake Superior region, North America. The Portage Lake Volcanics in Michigan, which are the younget MRS flood basalts, fall into distinctly high- and low-TiO2 types having different liquid lines of descent. Incompatible trace elements in both types of tholeiites are enriched compared to depleted or primitive mantle and both basalt types are isotopically indistinguishable. The isotopic enrichment of the MRS source compared to depleted mantle is striking and must have occurred at least 700 m.y. before 1100 Ma. There are two likely sources for such magmatism: subcontinental lithospheric mantle enriched during the early Proterozoic or enriched mantle derived from an upwelling plume. Decompression melting of an upwelling enriched mantle plume in a region of lithosphere thinned by extension could have successfully generated the enormous volume (850 ?? 103 km3) of relatively homogeneous magma in a restricted time interval. -from Authors

Radiogenic Ingrowth of 40CA from Decay of 40K Provides a Powerful Tracer for Understanding the Origins of Felsic Magmas

NASA Technical Reports Server (NTRS)

Mills, Ryan D.; Simon, Justin I.; Depaolo, Donald J.; Bachmann, Olivier

2013-01-01

Over time high K/Ca continental crust produces a unique Ca isotopic reservoir, with measurable 40Ca excesses compared to Earth's mantle (?Ca=0). Thus, values of ?Cai > 1 indicate a significant crustal contribution to a magma. Values of ?Cai (<1) indistinguishable from mantle Ca indicate that the Ca in those magmas is either directly from the mantle, or is from partial melting of newly formed crust. So, whereas 40Ca excesses clearly define crustal contributions, mantle-like 40Ca/44Ca ratios are not as definitive. Here we present Ca isotopic measurements of intermediate to felsic igneous rocks from the western United States, and two crustal xenoliths found within the Fish Canyon Tuff (FCT). The two crustal xenoliths found within the 28.2 Ma FCT of the southern Rocky Mountain volcanic field (SRMVF) yield ?Ca values of 4 and 7.5, respectively. The 40Ca excesses of these possible source rocks are due to long-term in situ 40K decay and suggest that they are Precambrian in age. However, the FCT (?Cai 0.3) is within uncertainty of the mantle 40Ca/44Ca. Together, these data indicate that little Precambrian crust was involved in the petrogenesis of the FCT. Nd isotopic analyses of the FCT imply that it was generated from 10- 75% of an enriched component, and the Ca isotopic data appear to restrict that component to newly formed lower crust, or enriched mantle. However, the Ca isotopic data do permit assimilation of some crust with low Ca/Nd; decreasing the 143Nd/144Nd without adding much excess 40Ca to the FCT. Several other large tuffs from the SRMVF and from Yellowstone have ?Cai indistinguishable from the mantle. However, a few large tuffs from the SRMVF show significant 40Ca excesses. These tuffs (Wall Mountain, Blue Mesa, and Grizzly Peak) are likely sourced from near, or within the Colorado Mineral Belt. New isotopic measurements of Mesozoic and Tertiary granites from across the northern Great Basin show a range of ?Cai from 0 to 3. In these samples ?Cai is generally correlated with ?Sri and is broadly negatively correlated with ?Ndi. However, for granites with similar ?Ndi at a given general location ?Cai can vary significantly (1 to 2 epsilon units). In rocks where low ?Ndi could also be due to melting from enriched reservoirs in the mantle lithosphere, the combination of high ?Cai with low ?Ndi clearly identifies crustal melts.

Continental crust beneath southeast Iceland.

PubMed

Torsvik, Trond H; Amundsen, Hans E F; Trønnes, Reidar G; Doubrovine, Pavel V; Gaina, Carmen; Kusznir, Nick J; Steinberger, Bernhard; Corfu, Fernando; Ashwal, Lewis D; Griffin, William L; Werner, Stephanie C; Jamtveit, Bjørn

2015-04-14

The magmatic activity (0-16 Ma) in Iceland is linked to a deep mantle plume that has been active for the past 62 My. Icelandic and northeast Atlantic basalts contain variable proportions of two enriched components, interpreted as recycled oceanic crust supplied by the plume, and subcontinental lithospheric mantle derived from the nearby continental margins. A restricted area in southeast Iceland--and especially the Öræfajökull volcano--is characterized by a unique enriched-mantle component (EM2-like) with elevated (87)Sr/(86)Sr and (207)Pb/(204)Pb. Here, we demonstrate through modeling of Sr-Nd-Pb abundances and isotope ratios that the primitive Öræfajökull melts could have assimilated 2-6% of underlying continental crust before differentiating to more evolved melts. From inversion of gravity anomaly data (crustal thickness), analysis of regional magnetic data, and plate reconstructions, we propose that continental crust beneath southeast Iceland is part of ∼350-km-long and 70-km-wide extension of the Jan Mayen Microcontinent (JMM). The extended JMM was marginal to East Greenland but detached in the Early Eocene (between 52 and 47 Mya); by the Oligocene (27 Mya), all parts of the JMM permanently became part of the Eurasian plate following a westward ridge jump in the direction of the Iceland plume.

Continental crust beneath southeast Iceland

PubMed Central

Torsvik, Trond H.; Amundsen, Hans E. F.; Trønnes, Reidar G.; Doubrovine, Pavel V.; Gaina, Carmen; Kusznir, Nick J.; Steinberger, Bernhard; Corfu, Fernando; Ashwal, Lewis D.; Griffin, William L.; Werner, Stephanie C.; Jamtveit, Bjørn

2015-01-01

The magmatic activity (0–16 Ma) in Iceland is linked to a deep mantle plume that has been active for the past 62 My. Icelandic and northeast Atlantic basalts contain variable proportions of two enriched components, interpreted as recycled oceanic crust supplied by the plume, and subcontinental lithospheric mantle derived from the nearby continental margins. A restricted area in southeast Iceland—and especially the Öræfajökull volcano—is characterized by a unique enriched-mantle component (EM2-like) with elevated 87Sr/86Sr and 207Pb/204Pb. Here, we demonstrate through modeling of Sr–Nd–Pb abundances and isotope ratios that the primitive Öræfajökull melts could have assimilated 2–6% of underlying continental crust before differentiating to more evolved melts. From inversion of gravity anomaly data (crustal thickness), analysis of regional magnetic data, and plate reconstructions, we propose that continental crust beneath southeast Iceland is part of ∼350-km-long and 70-km-wide extension of the Jan Mayen Microcontinent (JMM). The extended JMM was marginal to East Greenland but detached in the Early Eocene (between 52 and 47 Mya); by the Oligocene (27 Mya), all parts of the JMM permanently became part of the Eurasian plate following a westward ridge jump in the direction of the Iceland plume. PMID:25825769

Meteoritic Evidence for Multiple Early Enriched Reservoirs in the Martian Mantle

NASA Astrophysics Data System (ADS)

Armytage, R. M. G.; Debaille, V.; Brandon, A. D.; Agee, C. B.

2018-05-01

From isotopic systematics, the martian crustal reservoir represented by NWA 7034 cannot be the enriched end-member for the shergottites. This suggests multiple enriched reservoirs in the martian mantle formed by several differentiation events.

Dynamical Geochemistry

NASA Astrophysics Data System (ADS)

Davies, G. F.

2009-12-01

Dynamical and chemical interpretations of the mantle have hitherto remained incompatible, despite substantial progress over recent years. It is argued that both the refractory incompatible elements and the noble gases can be reconciled with the dynamical mantle when mantle heterogeneity is more fully accounted for. It is argued that the incompatible-element content of the MORB source is about double recent estimates (U~10 ng/g) because enriched components have been systematically overlooked, for three main reasons. (1) in a heterogeneous MORB source, melts from enriched pods are not expected to equilibrate fully with the peridotite matrix, but recent estimates of MORB-source composition have been tied to residual (relatively infertile) peridotite composition. (2) about 25% of the MORB source comes from plumes, but plume-like components have tended to be excluded. (3) a focus on the most common “normal” MORBs, allegedly representing a “depleted” MORB source, has overlooked the less-common but significant enriched components of MORBs, of various possible origins. Geophysical constraints (seismological and topographic) exclude mantle layering except for the thin D” layer and the “superpiles” under Africa and the Pacific. Numerical models then indicate the MORB source comprises the rest of the mantle. Refractory-element mass balances can then be accommodated by a MORB source depleted by only a factor of 2 from chondritic abundances, rather than a factor of 4-7. A source for the hitherto-enigmatic unradiogenic helium in OIBs also emerges from this picture. Melt from subducted oceanic crust melting under MORs will react with surrounding peridotite to form intemediate compositions here termed hybrid pyroxenite. Only about half of the hybrid pyroxenite will be remelted, extracted and degassed at MORs, and the rest will recirculate within the mantle. Over successive generations starting early in Earth history, volatiles will come to reside mainly in the hybrid pyroxenite. This will be denser than average mantle and will tend to accumulate in D”, like subducted oceanic crust. Because residence times in D” are longer, it will degas more slowly. Thus plumes will tap a mixture of older, less-degassed hybrid pyroxenite, containing less-radiogenic noble gases, and degassed former oceanic crust. Calculations of degassing history confirm that this picture can quantitatively account for He, Ne and Ar in MORBs and OIBs. Geophysically-based dynamical models have been shown over recent years to account quantitatively for the isotopes of refractory incompatible elements. This can now be extended to noble gas isotopes. The remaining significant issue is that thermal evolution calculations require more radiogenic heating than implied by cosmochemical estimates of radioactive heat sources. This may imply that tectonic and thermal evolution have been more episodic in the Phanerozoic than has been generally recognised.

Compositions of HIMU, EM1, and EM2 from Global Trends between Radiogenic Isotopes and Major Elements in Ocean Island Basalts

NASA Astrophysics Data System (ADS)

Jackson, M. G.; Dasgupta, R.

2008-12-01

Sr and Pb isotopes exhibit global trends with the concentrations of major elements (SiO2, TiO2, FeO, Al2O3 and K2O) and major elements ratios (CaO/Al2O3 and K2O/TiO2) in the shield-stage lavas from 18 oceanic hotspots (including Hawaii, Iceland, Galapagos, Cook-Australs, St. Helena, Cape Verde, Cameroon, Canary, Madeira, Comoros, Azores, Samoa, Society, Marquesas, Mascarene, Kerguelen, Pitcairn, and Selvagen). Based on the relationships between major elements and isotopes in ocean island basalts (OIBs), we find that the lavas derived from the mantle end members, HIMU (or high 'ì' = 238U/204Pb), EM1 (enriched mantle 1), EM2 (enriched mantle 2), and DMM (depleted MORB [mid-ocean ridge basalt] mantle) exhibit distinct major element characteristics: When compared to oceanic hotspots globally, the hotspots with a HIMU (radiogenic Pb-isotopes and low 87Sr/86Sr) component, such as St. Helena and Cook-Australs, exhibit high CaO/Al2O3, FeOT, and TiO2 and low SiO2 and Al2O3. EM1 (enriched mantle 1; intermediate 87Sr/86Sr and low 206Pb/204Pb; sampled by hotspots like Pitcairn and Kerguelen) and EM2 (enriched mantle 2; high 87Sr/86Sr and intermediate 206Pb/204Pb; sampled by hotspots like Samoa and Societies) exhibit higher K2O concentrations and K2O/TiO2 weight ratios than HIMU lavas. EM1 lavas exhibit the lowest CaO/Al2O3 in the OIB dataset, and this sets EM1 apart from EM2. A plot of CaO/Al2O3 vs K2O/TiO2 perfectly resolves the four mantle end member lavas. Melting processes (pressure, temperature and degree of melting) fail to provide an explanation for the full spectrum of major element concentrations in OIBs. Such processes also fail to explain the correlations between major elements and radiogenic isotopes. Instead, a long, time integrated history of various parent- daughter elements appears to be coupled to major element and/or volatile heterogeneity in the mantle source. End member lava compositions are compared with experimental partial melt compositions to place constraints on the lithological characteristics of the mantle end members.

Compositions of HIMU, EM1, and EM2 from global trends between radiogenic isotopes and major elements in ocean island basalts

NASA Astrophysics Data System (ADS)

Jackson, Matthew G.; Dasgupta, Rajdeep

2008-11-01

Sr and Pb isotopes exhibit global trends with the concentrations of major elements (SiO 2, TiO 2, FeO, Al 2O 3 and K 2O) and major elements ratios (CaO/Al 2O 3 and K 2O/TiO 2) in the shield-stage lavas from 18 oceanic hotspots (including Hawaii, Iceland, Galapagos, Cook-Australs, St. Helena, Cape Verde, Cameroon, Canary, Madeira, Comoros, Azores, Samoa, Society, Marquesas, Mascarene, Kerguelen, Pitcairn, and Selvagen). Based on the relationships between major elements and isotopes in ocean island basalts (OIBs), we find that the lavas derived from the mantle end members, HIMU (or high 'μ' = 238U/ 204Pb), EM1 (enriched mantle 1), EM2 (enriched mantle 2), and DMM (depleted MORB [mid-ocean ridge basalt] mantle) exhibit distinct major element characteristics: When compared to oceanic hotspots globally, the hotspots with a HIMU (radiogenic Pb-isotopes and low 87Sr/ 86Sr) component, such as St. Helena and Cook-Australs, exhibit high CaO/Al 2O 3, FeO T, and TiO 2 and low SiO 2 and Al 2O 3. EM1 (enriched mantle 1; intermediate 87Sr/ 86Sr and low 206Pb/ 204Pb; sampled by hotspots like Pitcairn and Kerguelen) and EM2 (enriched mantle 2; high 87Sr/ 86Sr and intermediate 206Pb/ 204Pb; sampled by hotspots like Samoa and Societies) exhibit higher K 2O concentrations and K 2O/TiO 2 weight ratios than HIMU lavas. EM1 lavas exhibit the lowest CaO/Al 2O 3 in the OIB dataset, and this sets EM1 apart from EM2. A plot of CaO/Al 2O 3 vs K 2O/TiO 2 perfectly resolves the four mantle end member lavas. Melting processes (pressure, temperature and degree of melting) fail to provide an explanation for the full spectrum of major element concentrations in OIBs. Such processes also fail to explain the correlations between major elements and radiogenic isotopes. Instead, a long, time integrated history of various parent-daughter elements appears to be coupled to major element and/or volatile heterogeneity in the mantle source. End member lava compositions are compared with experimental partial melt compositions to place constraints on the lithological characteristics of the mantle end members.

Slab-derived components in the subcontinental lithospheric mantle beneath Chilean Patagonia: Geochemistry and Sr-Nd-Pb isotopes of mantle xenoliths and host basalt

NASA Astrophysics Data System (ADS)

Jalowitzki, Tiago; Gervasoni, Fernanda; Conceição, Rommulo V.; Orihashi, Yuji; Bertotto, Gustavo W.; Sumino, Hirochika; Schilling, Manuel E.; Nagao, Keisuke; Morata, Diego; Sylvester, Paul

2017-11-01

In subduction zones, ultramafic xenoliths hosted in alkaline basalts can yield significant information about the role of potential slab-derived components in the subcontinental lithospheric mantle (SCLM). Chemical and isotopic heterogeneities in such xenoliths are usually interpreted to reflect melt extraction followed by metasomatic re-enrichment. Here we report new whole-rock major, trace element and isotopic (Sr-Nd-Pb) data for a Proterozoic suite of 17 anhydrous spinel-lherzolites and Eocene (new K-Ar data) host alkaline basalt found near Coyhaique ( 46°S), Aysén Region, Chile. These Patagonian nodules are located in a current back-arc position, 100 km east of the present day volcanic arc and 320 km from the Chile Trench. The mantle xenoliths consist of coarse- to medium-grained spinel-lherzolites with trace element compositions characteristic of a subduction zone setting, such as pronounced negative Nb, Ta and Ti anomalies coupled with significant enrichment of LILEs (e.g., U) and chalcophile elements (W, Pb and Sn). Most of them are characterized by flat to depleted light-rare earth element (LREE) patterns (Ce/YbN = 0.6-1.1) coupled with less radiogenic Sr-Pb (87Sr/86Sr = 0.702422-0.703479; 206Pb/204Pb = 18.212-18.539) and more radiogenic Nd isotopic compositions (143Nd/144Nd = 0.512994-0.513242), similar to the depleted mantle component (DMM or PREMA). In contrast, samples with slight LREE enrichment (Ce/YbN = 1.3-1.8) show more radiogenic Sr-Pb (87Sr/86Sr = 0.703791-0.704239; 206Pb/204Pb = 18.572-18.703) and less radiogenic Nd isotopic compositions (143Nd/144Nd = 0.512859-0.512934), similar to the EM-2 reservoir. These new geochemical and isotope data suggest that the Coyhaique spinel-lherzolites are derived from a heterogeneous SCLM resulting from mixing between a depleted mantle component and up to 10% of slab-derived components. The enriched component added to the SCLM represents variable extents of melts of both subducted Chile Trench sediments and modified oceanic crust throughout the initial stages of the Farallón-Aluk ridge collision during Paleocene to Eocene time. However, based on the tectonic evolution of southern South America, we cannot exclude the influence of long-lived subduction events beneath south Patagonia. Although we believe that the studied samples were brought to the surface in this geodynamic context, there is no evidence that ocean island basalt (OIB)-like melts related to the Farallón-Aluk asthenospheric slab window affected the peridotite composition. The host alkaline basalt is a single unit with a HIMU-like OIB signature characterized by marked positive Nb-Ta anomalies coupled with negative anomalies in highly incompatible and fluid-mobile elements (Rb, K, Pb, and Sr). The compositional similarity between the HIMU-like OIB mantle source and the host basalt is also evident from trace element ratios [(Ba-Th-K-La-Zr)/Nb] as well as by the low 87Sr/86Sri (0.703039-0.703058) and relatively high 143Nd/144Ndi (0.512880-0.512874) and 206Pb/204Pb (19.333-19.389) isotopic ratios. The low 206Pb/204Pb ratios compared to end-member HIMU lavas (e.g., Sta. Helena and the Cook-Austral Islands) suggest that this region was modified by processes associated with a prolonged period of subduction related to the Andean orogenesis and the recycling of several oceanic plates beneath the continent, following the Mesozoic breakup of Gondwana or an even older subduction-related event with young recycling ages (< 2 Ga).

Mixing in heterogeneous internally-heated convection

NASA Astrophysics Data System (ADS)

Limare, A.; Kaminski, E. C.; Jaupart, C. P.; Farnetani, C. G.; Fourel, L.; Froment, M.

2017-12-01

Past laboratory experiments of thermo chemical convection have dealt with systems involving fluids with different intrinsic densities and viscosities in a Rayleigh-Bénard setup. Although these experiments have greatly improved our understanding of the Earth's mantle dynamics, they neglect a fundamental component of planetary convection: internal heat sources. We have developed a microwave-based method in order to study convection and mixing in systems involving two layers of fluid with different densities, viscosities, and internal heat production rates. Our innovative laboratory experiments are appropriate for the early Earth, when the lowermost mantle was likely enriched in incompatible and heat producing elements and when the heat flux from the core probably accounted for a small fraction of the mantle heat budget. They are also relevant to the present-day mantle if one considers that radioactive decay and secular cooling contribute both to internal heating. Our goal is to quantify how two fluid layers mix, which is still very difficult to resolve accurately in 3-D numerical calculations. Viscosities and microwave absorptions are tuned to achieve high values of the Rayleigh-Roberts and Prandtl numbers relevant for planetary convection. We start from a stably stratified system where the lower layer has higher internal heat production and density than the upper layer. Due to mixing, the amount of enriched material gradually decreases to zero over a finite time called the lifetime. Based on more than 30 experiments, we have derived a scaling law that relates the lifetime of an enriched reservoir to the layer thickness ratio, a, to the density and viscosity contrasts between the two layers, and to their two different internal heating rates in the form of an enrichment factor beta=1+2*a*H1/H, where H1 is the heating rate of the lower fluid and H is the average heating rate. We find that the lifetime of the lower enriched reservoir varies as beta**(-7/3) in the low viscosity contrast limit, and as beta**(-4/3) in the large viscosity contrast limit. Our state-of-the-art experimental technique thus provides insights on chemical differentiation processes and on the evolution of mantle heterogeneities on both short and long time-scales.

Elastic Properties of Orthoenstatite at Simultaneous High Pressure-Temperature Conditions and the Implication for the Origin of Low VP/VS Zones in the Mantle Wedge

NASA Astrophysics Data System (ADS)

Qian, W.; Wang, W.; Zou, F.; Wu, Z.

2017-12-01

The compositions of the Earth's interiors are critical in understanding the origin and evolution of the Earth and its geodynamics. Orthopyroxene is an important component for the upper mantle both in pyrolite model and in piclogite model. Furthermore, many evidences suggest the local enrichment of opx in the upper mantle. Therefore, its thermodynamic and elastic properties are fundamental for understanding of chemical compositions and dynamics of the upper mantle. We obtain the elastic properties of orthoenstatite (MgSiO3), Mg end-member orthopyroxene with space group Pbca, up to 20 GPa and 2000 K using first principles calculations with local density approximation (LDA). The calculated results are in good agreement with previous available experimental measurements and theoretical results. Both bulk and shear modulus show noticeable nonlinear pressure dependence, and the softening of shear wave velocities is prominent at high pressure. Meanwhile, orthoenstatite exhibits a negative temperature derivate of VP/VS ratios. This is different from other upper mantle minerals, such as olivine, ringwoodite and garnet, whose VP/VS increase with the increasing of the temperature. Compared to other major minerals in the upper mantle, orthoenstatite shows the lowest compressional velocities, shear velocities, and VP/VS (<1.7) ratio up to the depth of 200 km. Recently, many seismic studies have observed unusual low VP/VS (below 1.72) zones in subduction mantle wedge and orthopyroxene has been proposed to be a possible interpretation of this unusual observed. However, this explanation is still under debate because no experimental or calculated elastic data at the conditions of the upper mantle are available before. Our calculations show that VS and VP/VS ratio of orthoenstatite under the mantle wedge conditions (2-3 GPa and 1073-1723 K) are consistent of the unusual seismic observations of VP/VS in subduction mantle wedge. Therefore, the enrichment of orthopyroxene may potentially account for the observed low VP/VS in the mantle wedge.

Geochemical nature of sub-ridge mantle and opening dynamics of the South China Sea

NASA Astrophysics Data System (ADS)

Zhang, Guo-Liang; Luo, Qing; Zhao, Jian; Jackson, Matthew G.; Guo, Li-Shuang; Zhong, Li-Feng

2018-05-01

The Indian-type mantle (i.e., above the north hemisphere reference line on the plot of 208Pb/204Pb vs. 206Pb/204Pb) has been considered as a "Southern Hemisphere" geochemical signature, whose origin remains enigmatic. The South China Sea is an extensional basin formed after rifting of the Euro-Asia continent in the Northern Hemisphere, however, the geochemical nature of the igneous crust remains unexplored. For the first time, IODP Expedition 349 has recovered seafloor basalts covered by the thick sediments in the Southwest sub-basin (Sites U1433 and U1434) and the East sub-basin (Site U1431). The Southwest sub-basin consists of enriched (E)-MORB type basalts, and the East sub-basin consists of both normal (N)-MORB-type and E-MORB-type basalts based on trace element compositions. The basalts of the two sub-basins are Indian-type MORBs based on Sr-Nd-Pb-Hf isotope compositions, and the Southwest sub-basin basalts show isotopic compositions (i.e., 206Pb/204Pb of 17.59-17.89) distinctly different from the East sub-basin (i.e., 206Pb/204Pb of 18.38-18.57), suggesting a sub-basin scale mantle compositional heterogeneity and different histories of mantle compositional evolution. Two different enriched mantle end-members (EM1 and EM2) are responsible for the genesis of the Indian-type mantle in the South China Sea. We have modeled the influences of Hainan mantle plume and lower continental crust based on Sr-Nd-Pb-Hf isotope compositions. The results indicate that the influence of Hainan plume can explain the elevated 206Pb/204Pb of the East sub-basin basalts, and the recycling of lower continental crust can explain the low 206Pb/204Pb of the Southwest sub-basin basalts. Based on the strong geochemical imprints of Hainan plume in the ridge magmatism, we propose that the Hainan plume might have promoted the opening of the South China Sea, during which the Hainan plume contributed enriched component to the sub-ridge mantle and caused thermal erosion and return of lower continental crust to the convective mantle. These results imply an in situ origin of the Indian-type mantle that can help understand the genesis of the "Southern Hemisphere" geochemical anomaly in the Northern Hemispheric extensional basin.

Valence State Partitioning of Cr and V Between Pyroxene - Melt: Estimates of Oxygen Fugacity for Martian Basalt QUE 94201

NASA Technical Reports Server (NTRS)

Karner, J. M.; Papike, J. J.; Shearer, C. K.; McKay, G.; Le, L.; Burger, P.

2007-01-01

Several studies, using different oxybarometers, have suggested that the variation of fO2 in martian basalts spans about 3 log units from approx. IW-1 to IW+2. The relatively oxidized basalts (e.g., pyroxene-phyric Shergotty) are enriched in incompatible elements, while the relatively reduced basalts (e.g., olivine-phyric Y980459) are depleted in incompatible elements. A popular interpretation of the above observations is that the martian mantle contains two reservoirs; 1) oxidized and enriched, and 2) reduced and depleted. The basalts are thus thought to represent mixing between these two reservoirs. Recently, Shearer et al. determined the fO2 of primitive olivine-phyric basalt Y980459 to be IW+0.9 using the partitioning of V between olivine and melt. In applying this technique to other basalts, Shearer et al. concluded that the martian mantle shergottite source was depleted and varied only slightly in fO2 (IW to IW+1). Thus the more oxidized, enriched basalts had assimilated a crustal component on their path to the martian surface. In this study we attempt to address the above debate on martian mantle fO2 using the partitioning of Cr and V into pyroxene in pyroxene-phyric basalt QUE 94201.

Phase equilibria and geochemical constraints on the petrogenesis of high-Ti picrite from the Paleogene East Greenland flood basalt province

NASA Astrophysics Data System (ADS)

Zhang, Yi-Shen; Hou, Tong; Veksler, Ilya V.; Lesher, Charles E.; Namur, Olivier

2018-02-01

Phase equilibrium experiments have been performed on an extremely high-Ti (5.4 wt.% TiO2) picrite from the base of the Paleogene ( 55 Ma) East Greenland Flood Basalt Province. This sample has a high CaO/Al2O3 ratio (1.14), a steep rare-earth elements (REE) profile, is enriched in incompatible trace elements, and is in chemical equilibrium with highly primitive olivine. This all suggests that the picrite is a near-primary melt that did not suffer major chemical evolution during ascent from the mantle source and through the crust. Near-liquidus phase relations were determined over the pressure range of 1 atm, 1 to 1.5 GPa and at temperatures from 1094 to 1400°C. They provide an important constraint on the petrogenesis of these lavas. The high-Ti picritic melt is multi-saturated with olivine (Ol) + orthopyroxene (Opx) at 1 GPa but has only Ol or Opx on the liquidus at lower and higher pressures, respectively. This indicates the primitive melt was last equilibrated with its mantle source at relatively shallow pressure ( 1 GPa). Melting probably started at 2-3 GPa and the picritic melt was produced by 15-30% melting of the mantle source. Such a degree of partial melting requires a mantle with a high potential temperature (1480-1530˚C). The relatively low CaO content and high FeO/MnO ratios of the most primitive East Greenland picrites, the high Ni content of olivine phenocrysts and the presence of low-Ca pyroxene (i.e., pigeonite) at high pressure in our experiments all suggest that the mantle source contained a major component of garnet pyroxenite. Residual garnet in the source could adequately explain the low Al2O3 content (7.92 wt.%) and steep REE patterns of the picrite sample. However, simple melting of a lherzolitic source, even with a major pyroxenite component, cannot explain the formation of magmas with the very high Ti contents observed in some East Greenland basalts. We therefore propose that magmas highly-enriched in Ti were produced by melting of a metasomatized mantle source containing Ti-enriched amphibole and/or phlogopite.

Silicon Isotope Geochemistry of Ocean Island Basalts: Mantle Heterogeneities and Contribution of Recycled Oceanic Crust and Lithosphere

NASA Astrophysics Data System (ADS)

Pringle, E. A.; Moynier, F.; Savage, P. S.; Jackson, M. G.; Moreira, M. A.; Day, J. M.

2015-12-01

The study of Silicon (Si) isotopes in Ocean Island Basalts (OIB) has the potential to elucidate between possible heterogeneities in the mantle. Relatively large (~several per mil per atomic mass unit) Si isotope fractionation occurs in low-temperature environments during biochemical and geochemical precipitation of dissolved Si, where the precipitate is preferentially enriched in the lighter isotopes [1]. In contrast, only a limited range (~tenths of a per mil) of Si isotope fractionation has been observed in high-temperature igneous processes [2]. Therefore, Si isotopes may be useful as tracers for the presence of crustal material (derived from low-temperature surface processes) in OIB source regions in a manner similar to more conventional stable isotope systems, such as O. Here we present the first comprehensive set of high-precision Si isotope data obtained by MC-ICP-MS for a diverse suite of OIBs, including new data for the Canary Islands. Samples represent the Pacific, Atlantic, and Indian Ocean basins and include representative end-members for the EM-1, EM-2, and HIMU mantle components. Average δ30Si values for OIBs representing the EM-1 (-0.32 ± 0.06‰, 2 sd), EM-2 (-0.30 ± 0.01‰, 2 sd), and HIMU (-0.34 ± 0.09‰, 2 sd) mantle components are all in general agreement with previous estimates for the δ30Si value of Bulk Silicate Earth [3]. However, small systematic variations are present; HIMU (Mangaia, Cape Verde, La Palma) and Iceland OIBs are enriched in the lighter isotopes of Si (δ30Si values lower than MORB). Further, the difference in Si isotope composition between La Palma and El Heirro (Canary Islands) has previously been observed for O isotopes [4], suggesting a relationship between the Si and O isotope mantle systematics. The Si isotope variations among OIBs may be explained by the sampling of a primitive mantle reservoir enriched in the light isotopes of Si, as suggested by [5], but most likely reflects the incorporation of recycled altered oceanic crust and lithosphere in the plume source. References: [1] Ziegler et al., GCA 2005 [2] Savage et al., GCA 2011 [3] Savage et al., EPSL 2010 [4] Day et al., Geology 2009 [5] Huang et al., GCA 2014

Petrological systematics of mid-ocean ridge basalts: Constraints on melt generation beneath ocean ridges

NASA Astrophysics Data System (ADS)

Langmuir, Charles H.; Klein, Emily M.; Plank, Terry

Mid-ocean ridge basalts (MORB) are a consequence of pressure-release melting beneath ocean ridges, and contain much information concerning melt formation, melt migration and heterogeneity within the upper mantle. MORB major element chemical systematics can be divided into global and local aspects, once they have been corrected for low pressure fractionation and interlaboratory biases. Regional average compositions for ridges unaffected by hot spots ("normal" ridges) can be used to define the global correlations among normalized Na2O, FeO, TiO2 and SiO2 contents, CaO/Al2O3 ratios, axial depth and crustal thickness. Back-arc basins show similar correlations, but are offset to lower FeO and TiO2 contents. Some hot spots, such as the Azores and Galapagos, disrupt the systematics of nearby ridges and have the opposite relationships between FeO, Na2O and depth over distances of 1000 km. Local variations in basalt chemistry from slow- and fast-spreading ridges are distinct from one another. On slow-spreading ridges, correlations among the elements cross the global vector of variability at a high angle. On the fast-spreading East Pacific Rise (EPR), correlations among the elements are distinct from both global and slow-spreading compositional vectors, and involve two components of variation. Spreading rate does not control the global correlations, but influences the standard deviations of axial depth, crustal thickness, and MgO contents of basalts. Global correlations are not found in very incompatible trace elements, even for samples far from hot spots. Moderately compatible trace elements for normal ridges, however, correlate with the major elements. Trace element systematics are significantly different for the EPR and the mid-Atlantic Ridge (MAR). Normal portions of the MAR are very depleted in REE, with little variability; hot spots cause large long wavelength variations in REE abundances. Normal EPR basalts are significantly more enriched than MAR basalts from normal ridges, and still more enriched basalts can erupt sporadically along the entire length of the EPR. This leads to very different histograms of distribution for the data sets as a whole, and a very different distribution of chemistry along strike for the two ridges. Despite these differences, the mean Ce/Sm ratios from the two ridges are identical. Existing methods for calculating the major element compositions of mantle melts [Klein and Langmuir, 1987; McKenzie and Bickle, 1988; Niu and Batiza, 1991] are critically examined. New quantitative methods for mantle melting and high pressure fractionation are developed to evaluate the chemical consequences of melting and fractionation processes and mantle heterogeneity. The new methods rely on new equations for partition coefficients for the major elements between mantle minerals and melts. The melting calculations can be used to investigate the chemical compositions produced by small extents of melting or high pressures of melting that cannot yet be determined experimentally. Application of the new models to the observations described above leads to two major conclusions: (1) The global correlations for normal ridges are caused by variations in mantle temperature, as suggested by Klein and Langmuir [1987] and not by mantle heterogeneity. (2) Local variations are caused by melting processes, but are not yet quantitatively accounted for. On slower spreading ridges, local variations are controlled by the melting regime in the mantle. On the EPR, local variations are predominantly controlled by ubiquitous, small scale heterogeneites. Volatile content may be an important and as yet undetermined factor in affecting the observed variations in major elements. We propose a hypothesis, similar to one proposed by Allegre et al [1984] for isotopic data, to explain the differences between the Atlantic and Pacific local trends, and the trace element systematics of the two ocean basins, as consequences of spreading rate and a different distribution of enriched components from hot spots in the two ocean basins. In the Atlantic, the hot spot influence is in discrete areas, and produces clear depth and chemical anomalies. Ridge segments far from hot spots do not contain enriched basalts. Melting processes associated with slow-spreading ridges vary substantially over short distances along strike and lead to the local trends discussed above, irrespective of hot spot influence. In the Pacific, enriched components appear to have been more thoroughly mixed into the mantle, leading to ubiquitous small scale heterogeneities. Melting processes do not vary appreciably along strike, so local chemical variations are dominated by the relative contribution of enriched component on short time and length scales. Thus the extent of mixing and distribution of enriched components influences strongly the contrasting local major element trends. Despite the difference in the distribution of enriched components, the mean compositions of each data set are equivalent. This suggests that the hot spot influence is similar in the two ocean basins, but its distribution in the upper mantle is different. These contrasting relationships between hot spots and ridges may result from differences in both spreading rate and tectonic history. Unrecognized hot spots may play an important role in diverse aspects of EPR volcanism, and in the chemical systematics of the erupted basalts. The observations and successful models have consequences for melt formation and segregation. (1) The melting process must be closer to fractional melting than equilibrium melting. This result is in accord with inferences from abyssal peridotites [Johnson et al., 1990]. (2) Small melt fractions generated over a range of pressures must be extracted rapidly and efficiently from high pressures within the mantle without experiencing low pressure equilibration during ascent. This requires movement in large channels, and possibly more efficient extraction mechanisms than nonnally envisaged in porous flow models with small residual porosity. (3) Diverse melts from the melting regime produce variations in basalts that are observable at the surface. (4) Basalt data can be used to constrain the melting process (e.g. active vs. passive upwelling) and its relationship to segmentation. The data cannot be used to constrain the shape of the melting regime, however, for many shapes lead to similar chemical results. (5) Highly incompatible elements and U-series disequilibria results appear not yet to be explained by melting models, and may require additional processes not yet clearly envisaged.

Pb-isotopic Features of Primitive Rocks from Hess Deep: Distinguishing between EPR and Cocos-Nazca Mantle Source(s)

NASA Astrophysics Data System (ADS)

Jean, M. M.; Falloon, T.; Gillis, K. M.

2014-12-01

We have acquired high-precision Pb-isotopic signatures of primitive lithologies (basalts/gabbros) recovered from IODP Expedition 345.The Hess Deep Rift, located in the vicinity of the Galapagos triple junction (Cocos, Nazca, and Pacific), is viewed as one the best-studied tectonic windows into fast-spreading crust because a relatively young (<1.5 Ma) cross section of oceanic crust. This allows for (1) characterization of the mantle source(s) at Hess Deep, (2) insight into the extent of isotopic homogeneity or heterogeneity in the area, and (3) constrain the relative contributions from the intruding Cocos-Nazca spreading center. The observed Pb-isotopic variation at Hess Deep covers almost the entire range of EPR MORB (10°N to -5°S). Hess Deep samples range from 208Pb (37.3-38.25), 207Pb (15.47-15.58), 206Pb (17.69-18.91). These compositions suggest that this part of Hess Deep mantle is no more isotopically homogeneous than EPR mantle. Two distinct arrays are also observed: 208Pb-enriched (r2=0.985; n=30) and 208Pb-depleted (r2=0.988; n=6). The 208Pb/204Pb isotopes indicates that the Pb-source for some of the samples at Hess Deep had very low Th/U ratios, whereas other areas around the Galapagos microplate seem to have more "normal" ratios. These trends are less apparent when viewed with 207Pb-isotopes. Instead, the majority of basalts and gabbros follow the NHRL, however, at the depleted-end of this array a negative excursion to more enriched compositions is observed. This negative but linear trend could signify an alteration trend or mixing with an EMI-type mantle source, yet this mixing is not observed with 208Pb. This trend is also observed at Pito Deep, which has similar origins to Hess Deep (Barker et al., 2008; Pollack et al., 2009). The Galapagos region has been considered a testing ground for mixing of HIMU, Enriched Mantle, and Depleted Mantle reservoirs (e.g., Schilling et al., 2002). According to our data, however, an EPR-component must also be considered. We model Hess Deep Pb-isotopes as a 4-component system. EPR-DM-EM comprise a 'local' reservoir, but the majority of samples contain a mixture of modified-HIMU-EM-EPR, a product of incoming plume material entrained within the Galapagos Spreading Center.

Global structure of mantle isotopic heterogeneity and its implications for mantle differentiation and convection

NASA Astrophysics Data System (ADS)

Iwamori, Hikaru; Albaréde, Francis; Nakamura, Hitomi

2010-11-01

In order to further our understanding of the global geochemical structure and mantle dynamics, a global isotopic data set of oceanic basalts was analyzed by Independent Component Analysis (ICA), a relatively new method of multivariate analysis. The data set consists of 2773 mid-ocean ridge basalts (MORB) and 1515 ocean island basalts (OIB) with five isotopic ratios of Pb, Nd and Sr. The data set spatially covers the major oceans and enables us to compare the results with global geophysical observations. Three independent components (ICs) have been found, two of which are essentially identical to those previously found for basalts from the Atlantic and Indian Oceans. The two ICs (IC1 and IC2) span a compositional plane that accounts for 95.7% of the sample variance, while the third IC (IC3) accounts for 3.7%. Based on the geochemical nature of ICs and a forward model concerning trace elemental and isotopic compositions, the origin of the ICs is discussed. IC1 discriminates OIB from MORB, and may be related to elemental fractionation associated with melting and the subsequent radiogenic in growth with an average recycling time of 0.8 to 2.4 Ga. IC2 tracks the regional provenance of both MORB and OIB and may be related to aqueous fluid-rock interaction and the subsequent radiogenic ingrowth with an average recycling time of 0.3 to 0.9 Ga. IC3 fingerprints upper continental crustal material and its high value appears in limited geographical and tectonic settings. Variations in the melt component (IC1) and in the aqueous fluid component (IC2) inherited in the mantle most likely reflect mid-ocean ridge and subduction zone processes, respectively. Long-term accumulation of dense materials rich in the IC1 melt component at the base of the convective mantle accounts for its longer recycling time with respect to that for less dense materials rich in the aqueous fluid component (IC2). IC2 broadly correlates with the seismic velocity structures of the lowermost mantle and electric conductivity around the mantle transition zones. We propose that IC2 reflects hydrogen distribution within the mantle and that several global domains enriched in hydrogen could exist as vertical sectors extending all the way down to the core-mantle boundary.

Coupled Hf-Nd-Pb isotope co-variations of HIMU oceanic island basalts from Mangaia, Cook-Austral islands, suggest an Archean source component in the mantle transition zone

NASA Astrophysics Data System (ADS)

Nebel, Oliver; Arculus, Richard J.; van Westrenen, Wim; Woodhead, Jon D.; Jenner, Frances E.; Nebel-Jacobsen, Yona J.; Wille, Martin; Eggins, Stephen M.

2013-07-01

Although it is widely accepted that oceanic island basalts (OIB) sample geochemically distinct mantle reservoirs including recycled oceanic crust, the composition, age, and locus of these reservoirs remain uncertain. OIB with highly radiogenic Pb isotope signatures are grouped as HIMU (high-μ, with μ = 238U/204Pb), and exhibit unique Hf-Nd isotopic characteristics, defined as ΔɛHf, deviant from a terrestrial igneous rock array that includes all other OIB types. Here we combine new Hf isotope data with previous Nd-Pb isotope measurements to assess the coupled, time-integrated Hf-Nd-Pb isotope evolution of the most extreme HIMU location (Mangaia, French Polynesia). In comparison with global MORB and other OIB types, Mangaia samples define a unique trend in coupled Hf-Nd-Pb isotope co-variations (expressed in 207Pb/206Pb vs. ΔɛHf). In a model employing subducted, dehydrated oceanic crust, mixing between present-day depleted MORB mantle (DMM) and small proportions (˜5%) of a HIMU mantle endmember can re-produce the Hf-Nd-Pb isotope systematics of global HIMU basalts (sensu stricto; i.e., without EM-1/EM-2/FOZO components). An age range of 3.5 to <2 Ga is required for HIMU endmember(s) that mix with DMM to account for the observed present-day HIMU isotope compositions, suggesting a range of age distributions rather than a single component in the mantle. Our data suggest that mixing of HIMU mantle endmembers and DMM occurs in the mantle transition zone by entrainment in secondary plumes that rise at the edge of the Pacific Large Low Seismic Velocity Zone (LLSVP). These create either pure HIMU (sensu stricto) or HIMU affected by other enriched mantle endmembers (sensu lato). If correct, this requires isolation of parts of the mantle transition zone for >3 Gyr and implies that OIB chemistry can be used to test geodynamic models.

Chemical provinces and dynamic melting of the NE Atlantic mantle

NASA Astrophysics Data System (ADS)

Tronnes, R. G.

2009-12-01

Low-degree melting of fertile parts of the NE Atlantic mantle yields primitive alkaline basalts in the Icelandic off-rift zones and at Jan Mayen. Olivine tholeiites in the Icelandic rift zones and oceanic spreading ridges are formed by protracted decompressional melting. The V-shaped ridges SW and NE of Iceland indicate that rising, hot material is supplied by a pulsating plume and deflected laterally for distances of about 1000 km from Iceland (Jones et al. GGG 2002; Breivik et al. JGR 2006). Plume material deflected along the rift zones and spreading ridges undergoes mixing with the ambient asthenosphere and extensive melting at shallow level, whereas material deflected in other directions may flow laterally at deeper levels and remain largely unmelted and fertile. A recent investigation of a suite of primitive off-rift basalts from Iceland and Jan Mayen (Debaille et al., 2009, GCA) demonstrated an important source contribution from subcontinental lithospheric mantle (SCLM). Available data on the primitive off-rift basalts and tholeiitic basalts from Iceland and the NE Atlantic ridges indicates the existence of three main composite mantle components, characterized by the following relative isotope ratios (H: high, I: intermediate and L: low ratio) for 87/86Sr, 143/144Nd, 206/204Pb, 187/188Os and 3/4He, respectively: 1. Iceland plume with depleted lower mantle mixed with recycled oceanic crust: I, I, H, H, H 2. Strongly depleted and later re-enriched SCLM: H, L, I, L, L 3. Depleted asthenosphere: L, H, L, I, L The two first composite components contain enriched and depleted subcomponents with distinct isotope signatures. The isotope ratio variations between the fertile components are larger than between the refractory components. The 3/4He ratio, however, is much higher in the depleted plume component than in the depleted SCLM and asthenospheric components. The old SCLM material could in principle be recycled and embedded in the lower mantle and supplied to the melting zone by the Iceland plume. However, a regional isotopic variation pattern indicates that this material originated from the nearby continents and became partially delaminated and embedded in the upper mantle during the recent continental rifting and separation of Greenland the Jan Mayen Ridge and of Greenland and Spitsbergen. The influence of SCLM is most clearly recognized north of central Iceland, in the Northern Rift Zone, along the Kolbeinsey, Mohns, Knipovich and Gakkel Ridges, and especially at Jan Mayen and along the westernmost Gakkel Ridge close to the Yermak Plateau (Goldstein et al. 2008, Nature). The SCLM-signal is weaker for Snæfellsnes, the Mid-Icelandic Belt and the Western and Eastern Rift Zones, and weakest for Vestmannaeyjar, the Southern Volcanic Flank Zone, the Reykjanes Peninsula and the Reykjanes Ridge. The regional geochemical patterns have interesting implications for the probable interaction between lateral plume flow, ridge-focussed asthenospheric flow and delaminated patches of SCLM.

Lithospheric mantle evolution in the Afro-Arabian domain: Insights from Bir Ali mantle xenoliths (Yemen)

NASA Astrophysics Data System (ADS)

Sgualdo, P.; Aviado, K.; Beccaluva, L.; Bianchini, G.; Blichert-Toft, J.; Bryce, J. G.; Graham, D. W.; Natali, C.; Siena, F.

2015-05-01

Detailed petrological and geochemical investigations of an extensive sampling of mantle xenoliths from the Neogene-Quaternary Bir Ali diatreme (southern Yemen) indicate that the underlying lithospheric mantle consists predominantly of medium- to fine-grained (often foliated) spinel-peridotites (85-90%) and spinel-pyroxenites (10-15%) showing thermobarometric estimates in the P-T range of 0.9-2.0 GPa and 900-1150 °C. Peridotites, including lherzolites, harzburgites and dunites delineate continuous chemical, modal and mineralogical variations compatible with large extractions of basic melts occurring since the late Proterozoic (~ 2 Ga, according to Lu-Hf model ages). Pyroxenites may represent intrusions of subalkaline basic melts interacting and equilibrated with the host peridotite. Subsequent metasomatism has led to modal changes, with evidence of reaction patches and clinopyroxene and spinel destabilization, as well as formation of new phases (glass, amphibole and feldspar). These changes are accompanied by enrichment of the most incompatible elements and isotopic compositions. 143Nd/144Nd ranges from 0.51419 to 0.51209 (εNd from + 30.3 to - 10.5), 176Hf/177Hf from 0.28459 to 0.28239 (εHf from + 64.4 to - 13.6), and 208Pb/204Pb from 36.85 to 41.56, thus extending from the depleted mantle (DM) towards the enriched OIB mantle (EM and HIMU) components. 3He/4He (R/RA) ratios vary from 7.2 to 7.9 with He concentrations co-varying with the most incompatible element enrichment, in parallel with metasomatic effects. These metasomatic events, particularly effective in harzburgites and dunites, are attributable to the variable interaction with alkaline basic melts related to the general extensional and rifting regime affecting the East Africa-Arabian domain during the Cenozoic. In this respect, Bir Ali mantle xenoliths resemble those occurring along the Arabian margins and the East Africa Rift system, similarly affected by alkaline metasomatism, whereas they are distinctly different from xenoliths located within the Ethiopian-Yemen continental flood basalt province that are pervasively refertilized by plume-related subalkaline melts.

Volcanology: Petit spots go big

NASA Astrophysics Data System (ADS)

Snow, Jonathan E.

2016-12-01

Mantle enrichment processes were thought to be limited to parts of oceanic plates influenced by plumes and to continental interiors. Analyses of mantle fragments of the Pacific Plate suggest that such enrichment processes may operate everywhere.

Compositional mantle layering revealed by slab stagnation at ~1000-km depth

PubMed Central

Ballmer, Maxim D.; Schmerr, Nicholas C.; Nakagawa, Takashi; Ritsema, Jeroen

2015-01-01

Improved constraints on lower-mantle composition are fundamental to understand the accretion, differentiation, and thermochemical evolution of our planet. Cosmochemical arguments indicate that lower-mantle rocks may be enriched in Si relative to upper-mantle pyrolite, whereas seismic tomography images suggest whole-mantle convection and hence appear to imply efficient mantle mixing. This study reconciles cosmochemical and geophysical constraints using the stagnation of some slab segments at ~1000-km depth as the key observation. Through numerical modeling of subduction, we show that lower-mantle enrichment in intrinsically dense basaltic lithologies can render slabs neutrally buoyant in the uppermost lower mantle. Slab stagnation (at depths of ~660 and ~1000 km) and unimpeded slab sinking to great depths can coexist if the basalt fraction is ~8% higher in the lower mantle than in the upper mantle, equivalent to a lower-mantle Mg/Si of ~1.18. Global-scale geodynamic models demonstrate that such a moderate compositional gradient across the mantle can persist can in the presence of whole-mantle convection. PMID:26824060

Isotopic and trace element geochemistry of the Seligdar magnesiocarbonatites (South Yakutia, Russia): Insights regarding the mantle evolution beneath the Aldan-Stanovoy shield

NASA Astrophysics Data System (ADS)

Doroshkevich, Anna G.; Prokopyev, Ilya R.; Izokh, Andrey E.; Klemd, Reiner; Ponomarchuk, Anton V.; Nikolaeva, Irina V.; Vladykin, Nikolay V.

2018-04-01

The Paleoproterozoic Seligdar magnesiocarbonatite intrusion of the Aldan-Stanovoy shield in Russia underwent extensive postmagmatic hydrothermal alteration and metamorphic events. This study comprises new isotopic (Sr, Nd, C and O) data, whole-rock major and trace element compositions and trace element characteristics of the major minerals to gain a better understanding of the source and the formation process of the carbonatites. The Seligdar carbonatites have high concentrations of P2O5 (up to 18 wt%) and low concentrations of Na, K, Sr and Ba. The chondrite-normalized REE patterns of these carbonatites display significant enrichments of LREE relative to HREE with an average La/Ybcn ratio of 95. Hydrothermal and metamorphic overprints changed the trace element characteristics of the carbonatites and their minerals. These alteration processes were responsible for Sr loss and the shifting of the Sr isotopic compositions towards more radiogenic values. The altered carbonatites are further characterized by distinct 18O- and 13C-enrichments compared to the primary igneous carbonatites. The alteration most likely resulted from both the percolation of crustal-derived hydrothermal fluids and subsequent metamorphic processes accompanied by interaction with limestone-derived CO2. The narrow range of negative εNd(T) values indicates that the Seligdar carbonatites are dominated by a homogenous enriched mantle source component that was separated from the depleted mantle during the Archean.

Tungsten Abundances in Hawaiian Picrites: Implications for the Mantle Sources of Hawaiian Volcanoes

NASA Astrophysics Data System (ADS)

Ireland, T. J.; Arevalo, R. D.; Walker, R. J.; McDonough, W. F.

2008-12-01

Tungsten abundances have been measured in a suite of Hawaiian picrites (MgO >13 wt.%) from nine Hawaiian shield volcanoes (Mauna Kea, Mauna Loa, Hualalai, Loihi, Koolau, Kilauea, Kohala, Lanai and Molokai). Tungsten concentrations in the parental melts for these volcanoes have been estimated via the intersection of linear W-MgO trends with the putative MgO content of the parental melt (~16 wt.%). Tungsten behaves as a highly incompatible trace element in mafic to ultramafic systems; thus, given an independent assessment of the degree of partial melting for each volcanic center, the W abundances in their mantle sources can be determined. The mantle sources for Hualalai, Kilauea, Kohala and Loihi have non- uniform estimated W abundances of 11, 13, 16 and 27 ng/g, respectively, giving an average source abundance of 17±5 ng/g. This average source abundance is nearly six times more enriched than Depleted MORB Mantle (DMM: 3.0±2.3 ng/g) and slightly elevated relative to the Bulk Silicate Earth (BSE: 13±10 ng/g). The relatively high abundances of W in the Hawaiian sources relative to the DMM can potentially be explained as a consequence of crustal recycling. For example, incorporation of 30% oceanic crust (30 ng/g W), including 3% sediment (1500 ng/g W), into a DMM source could create the W enrichment observed in the Loihi source, consistent with estimates from earlier models based on other trace elements and isotope systems. The Hualalai source, however, has also been suggested to contain a substantial recycled component, as implied by similarly radiogenic 187Os/188Os, yet this source has the lowest estimated W abundance among the volcanic centers studied. The conflict between these results may: 1) reflect chemical differences among recycled components, 2) indicate a more complex history for Hualalai samples, e.g. involvement of a melt percolation component, or 3) implicate other sources of W.

Tracking the source of the enriched martian meteorites in olivine-hosted melt inclusions of two depleted shergottites, Yamato 980459 and Tissint

NASA Astrophysics Data System (ADS)

Peters, T. J.; Simon, J. I.; Jones, J. H.; Usui, T.; Moriwaki, R.; Economos, R. C.; Schmitt, A. K.; McKeegan, K. D.

2015-05-01

The apparent lack of plate tectonics on all terrestrial planets other than Earth has been used to support the notion that for most planets, once a primitive crust forms, the crust and mantle evolve geochemically-independent through time. This view has had a particularly large impact on models for the evolution of Mars and its silicate interior. Recent data indicating a greater potential that there may have been exchange between the martian crust and mantle has led to a search for additional geochemical evidence to support the alternative hypothesis, that some mechanism of crustal recycling may have operated early in the history of Mars. In order to study the most juvenile melts available to investigate martian mantle source(s) and melting processes, the trace element compositions of olivine-hosted melt inclusions for two incompatible-element-depleted olivine-phyric shergottites, Yamato 980459 (Y98) and Tissint, and the interstitial glass of Y98, have been measured by Secondary Ionization Mass Spectrometry (SIMS). Chondrite-normalized Rare Earth Element (REE) patterns for both Y98 and Tissint melt inclusions, and the Y98 interstitial glass, are characteristically light-REE depleted and parallel those of their host rock. For Y98, a clear flattening and upward inflection of La and Ce, relative to predictions based on middle and heavier REE, provides evidence for involvement of an enriched component early in their magmatic history; either inherited from a metasomatized mantle or crustal source, early on and prior to extensive host crystallization. Comparing these melt inclusion and interstitial glass analyses to existing melt inclusion and whole-rock data sets for the shergottite meteorite suite, defines mixing relationships between depleted and enriched end members, analogous to mixing relationships between whole rock Sr and Nd isotopic measurements. When considered in light of their petrologic context, the origin of these trace element enriched and isotopically evolved signatures represents either (1) crustal assimilation during the final few km of melt ascent towards the martian surface, or (2) assimilation soon after melt segregation, through melt-rock interaction with a portion of the martian crust recycled back into the mantle.

Stages of weathering mantle formation from carbonate rocks in the light of rare earth elements (REE) and Sr-Nd-Pb isotopes

NASA Astrophysics Data System (ADS)

Hissler, Christophe; Stille, Peter

2015-04-01

Weathering mantles are widespread and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual high content of associated trace elements in weathering mantles originating from carbonate rocks, which have been poorly studied, compared to those developing on magmatic bedrocks. For instance, these enrichments can be up to five times the content of the underlying carbonate rocks. However, these studies also showed that the carbonate bedrock content only partially explains the soil enrichment for all the considered major and trace elements. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources. REE distribution patterns and Sr-Nd-Pb isotope ratios have been used because they are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments have been applied to identify mobile phases in the soil system and to yield information on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. All these geochemical informations indicate that the cambisol developing on such a typical weathering mantle ("terra fusca") has been formed through weathering of a condensed Bajocian limestone-marl facies. This facies shows compared to average world carbonates important trace element enrichments. Their trace element distribution patterns are similar to those of the soil suggesting their close genetic relationships. Sr-Nd-Pb isotope data allow to identify four principal components in the soil: a silicate-rich pool at close to the surface, a leachable REE enriched pool at the bottom of the soil profile, the limestone facies on which the weathering profile developed and an anthropogenic, atmosphere-derived component detected in the soil leachates of the uppermost soil horizon. The leachable phases are mainly secondary carbonate-bearing REE phases such as bastnaesite. The isotope data and trace element distribution patterns indicate that at least four geological and environmental events impacted the chemical and isotopical compositions of the soil system since the Cretaceous.

Geochemistry of NE Atlantic non-rifting zones, Iceland and Jan Mayen

NASA Astrophysics Data System (ADS)

Tronnes, R. G.; Waight, T.

2005-12-01

The fertile components of the NE Atlantic mantle are sampled preferentially by alkaline basalts in the volcanic flank zones of Iceland and in the Jan Mayen and Vesteris seamount areas. Our data from primitive flank zone lavas from Iceland and Jan Mayen demonstrate a HIMU-affinity with enrichment of HFSE, U/Pb, Th/U and Nb/Th. In PM-normalized spider diagrams the least enriched samples have weakly positive Sr-anomalies, whereas the most enriched samples have negative Sr-anomalies. The entire sample suite shows negative Sr-Nd-isotope correlation, whereas the samples of each volcanic system or flank zone generally lack such a correlation. Our data confirm the anomalously high 87/86Sr of the Orafajokull volcanic system in the eastern flank zone. The results are consistent with existing data for other primitive flank zone basalts from Iceland and Jan Mayen. Common geochemical features linking alkaline flank zone basalts and high-degree tholeiitic melts include high 87/86Sr (and probably 176/177Hf) for a given 143/144Nd, negative delta-207Pb (except for Orafajokull) and positive delta-Nb. Alkaline flank zone basalts have generally higher 87/86Sr, 206/204Pb and 18/16O and lower 143/144Nd, 187/188Os and 3/4He than rift zone tholeiites. The different 18/16O ratios in flank and rift zone basalts are consistent with seafloor hydrothermal alteration of the upper and lower parts of recycled oceanic lithosphere, respectively. Olivine-melt fractionation may contribute to the difference. Indications of lower 187/188Os in alkaline basalts compared to nearby rift zone tholeiites could be caused by subduction zone loss of Re from the upper part of recycled slabs. The partial melting and volcanic sampling of the fertile mantle components under Iceland and the NE Atlantic is governed by the crustal structure and geometry of the Icelandic volcanic zones and the lateral deflection of the upwelling heterogeneous mantle source originating under central Iceland. Based on the pattern of V-shaped ridges along the Kolbeinsey ridge, the lateral mantle flow from central Iceland may well extend beyond Jan Mayen. The geochemical similarities between the enriched basalts of the Icelandic flank zones and Jan Mayen support this contention, although a minor separate plume under JM is a possibility.

Implications of Nb/U, Th/U and Sm/Nd in plume magmas for the relationship between continental and oceanic crust formation and the development of the depleted mantle

NASA Astrophysics Data System (ADS)

Campbell, Ian H.

2002-05-01

The Nb/U and Th/U of the primitive mantle are 34 and 4.04 respectively, which compare with 9.7 and 3.96 for the continental crust. Extraction of continental crust from the mantle therefore has a profound influence on its Nb/U but little influence on its Th/U. Conversely, extraction of midocean ridge-type basalts lowers the Th/U of the mantle residue but has little influence on its Nb/U. As a consequence, variations in Th/U and Nb/U with Sm/Nd can be used to evaluate the relative importance of continental and basaltic crust extraction in the formation of the depleted (Sm/Nd enriched) mantle reservoir. This study evaluates Nb/U, Th/U, and Sm/Nd variations in suites of komatiites, picrites, and their associated basalts, of various ages, to determine whether basalt and/or continental crust have been extracted from their source region. Emphasis is placed on komatiites and picrites because they formed at high degrees of partial melting and are expected to have Nb/U, Th/U, and Sm/Nd that are essentially the same as the mantle that melted to produce them. The results show that all of the studied suites, with the exception of the Barberton, have had both continental crust and basaltic crust extracted from their mantle source region. The high Sm/Nd of the Gorgona and Munro komatiites require the elevated ratios seen in these suites to be due primarily to extraction of basaltic crust from their source regions, whereas basaltic and continental crust extraction are of subequal importance in the source regions of the Yilgarn and Belingwe komatiites. The Sm/Nd of modern midocean ridge basalts lies above the crustal extraction curve on a plot of Sm/Nd against Nb/U, which requires the upper mantle to have had both basaltic and continental crust extracted from it. It is suggested that the extraction of the basaltic reservoir from the mantle occurs at midocean ridges and that the basaltic crust, together with its complementary depleted mantle residue, is subducted to the core-mantle boundary. When the two components reach thermal equilibrium with their surroundings, the lighter depleted component separates from the denser basaltic component. Both are eventually returned to the upper mantle, but the lighter depleted component has a shorter residence time in the lower mantle than the denser basaltic component. If the difference in the recycling times for the basaltic and depleted components is ˜1.0 to 1.5 Ga, a basaltic reservoir is created in the lower mantle, equivalent to the amount of basalt that is subducted in 1.0 to 1.5 Ga, and that reservoir is isolated from the upper mantle. It is this reservoir that is responsible for the Sm/Nd ratio of the upper mantle lying above the trend predicted by extraction of continental crust on the plot of Sm/Nd against Nb/U.

Mantle plumes and hotspot geochemistry

NASA Astrophysics Data System (ADS)

Jackson, M. G.; Becker, T. W.; Konter, J.

2017-12-01

Ever improving global seismic models, together with expanding databases of mantle derived hotspot lavas, herald advances that relate the geochemistry of hotspots with low seismic shear-wave velocity conduits (plumes) in the mantle. Early efforts linked hotspot geochemistry with deep mantle large low velocity provinces (LLVPs) [1]. More recently, Konter and Becker (2012) [2] observed that the proportion of the C mantle component (inferred from Sr-Nd-Pb isotopes) in hotspot lavas shows an inverse relationship with seismic S-wave velocity anomalies in the shallow mantle (200 km) beneath each hotspot. They proposed that these correlations should also be made based on 3He/4He. Thus, we compare 3He/4He versus seismic S-wave velocity anomalies at 200 km depth. We find that plume-fed hotspots with the highest maximum 3He/4He (i.e., which host more of the C component) have higher hotspot buoyancy fluxes and overlie regions of lower seismic S-wave velocity (interpreted to relate to hotter mantle temperatures) at 200 km depth than hotspots that have only low 3He/4He [3]. This result complements recent work that shows an inverse relationship between maximum 3He/4He and seismic S-wave velocity anomalies in the mantle beneath the western USA [4]. The relationship between 3He/4He, shallow mantle seismic S-wave velocity anomalies, and buoyancy flux is most easily explained by a model where hotter plumes are more buoyant and entrain more of a deep, dense high 3He/4He reservoir than cooler plumes that underlie low 3He/4He hotspots. If the high 3He/4He domain is denser than other mantle components, it will be entrained only by the hottest, most buoyant plumes [3]. Such a deep, dense reservoir is ideally suited to preserving early-formed Hadean domains sampled in modern plume-fed hotspots. An important question is whether, like 3He/4He, seismic S-wave velocity anomalies in the mantle are associated with distinct heavy radiogenic isotopic compositions. C signatures are related to hot mantle upwellings, but are geochemically enriched (EM) and HIMU mantle signatures observed in oceanic hotspots associated with such upwellings? We will present new constraints on this and similar problems. [1] Castillo (1988) Nature 336. [2] Konter and Becker (2012) G-cubed 13. [3] Jackson et al. (2017), Nature 542. [4] Crossey et al. (2016), EPSL 435.

Partitioning of Large-ion Lithophile Elements Between Aqueous Fluids and Melts: Role of Saline Fluids in Sub-arc Mantle

NASA Astrophysics Data System (ADS)

Kawamoto, T.; Mibe, K.

2014-12-01

Chemical fractionation of slab-derived supercritical fluids can play an important role in elemental transfer from subducting slab to the mantle wedge and arc magmatism [1]. Recent findings of saline fluids from sub-arc mantle peridotite indicate that aqueous fluids in mantle wedge can contain 3.7 wt% NaCl in Ichinomageta, Northeast Japan arc [2] to 5.1 wt% NaCl in Pinatubo, Luzon arc [3]. It is, therefore, important to determine the effect of Cl on the trace element partitioning between aqueous fluids and melts. Synchrotron radiation X-ray fluorescence (XRF) analysis is conducted to know Rb, Sr, and Pb partitioning between aqueous fluids and melts [4]. There is a positive correlation between partition coefficients and pressure, as well as salinity. Two slab-derived components, melt and fluid components, are suggested to explain trace element characteristics of arc-basalts in the Mariana arc [5]. The fluid component is characterized by enrichment of alkali and alkali earth elements. Such features can be explained if the fluid component is a saline fluid, because alkali earth elements and Pb are much less mobile with Cl-free fluids than Cl-rich fluids [4]. We suggest that slab-derived components have compositional features consistent with a saline fluid and a melt, which can be formed through a separation of a slab-derived supercritical fluid [1]. Slab derived supercritical fluids contain Cl, and aqueous fluids inherit much of the Cl and some of the large-ion lithophile elements. [1] Kawamoto et al. 2012, Separation of supercritical slab-fluids to form aqueous fluid and melt components in subduction zone magmatism. PNAS, pnas.org/content/109/46/18695 [2] Kumagai et al. Evolution of carbon dioxide bearing saline fluids in the mantle wedge beneath the Northeast Japan arc, CMP [3] Kawamoto et al. 2013, Mantle wedge infiltrated with saline fluids from dehydration and decarbonation of subducting slab. PNAS, pnas.org/content/110/24/9663 [4] Kawamoto et al. 2014, Large ion lithophile elements delivered by saline fluids to the sub-arc mantle, EPS, earth-planets-space.com/content/66/1/61 [5] Pearce et al. 2005, Geochemical mapping of the Mariana arc-basin system: Implications for the nature and distribution of subduction components. G-cubed, onlinelibrary.wiley.com/doi/10.1029/2004GC000895/full

Evidence for chemically heterogeneous Arctic mantle beneath the Gakkel Ridge

NASA Astrophysics Data System (ADS)

D'Errico, Megan E.; Warren, Jessica M.; Godard, Marguerite

2016-02-01

Ultraslow spreading at mid-ocean ridges limits melting due to on-axis conductive cooling, leading to the prediction that peridotites from these ridges are relatively fertile. To test this, we examined abyssal peridotites from the Gakkel Ridge, the slowest spreading ridge in the global ocean ridge system. Major and trace element concentrations in pyroxene and olivine minerals are reported for 14 dredged abyssal peridotite samples from the Sparsely Magmatic (SMZ) and Eastern Volcanic (EVZ) Zones. We observe large compositional variations among peridotites from the same dredge and among dredges in close proximity to each other. Modeling of lherzolite trace element compositions indicates varying degrees of non-modal fractional mantle melting, whereas most harzburgite samples require open-system melting involving interaction with a percolating melt. All peridotite chemistry suggests significant melting that would generate a thick crust, which is inconsistent with geophysical observations at Gakkel Ridge. The refractory harzburgites and thin overlying oceanic crust are best explained by low present-day melting of a previously melted heterogeneous mantle. Observed peridotite compositional variations and evidence for melt infiltration demonstrates that fertile mantle components are present and co-existing with infertile mantle components. Melt generated in the Gakkel mantle becomes trapped on short length-scales, which produces selective enrichments in very incompatible rare earth elements. Melt migration and extraction may be significantly controlled by the thick lithosphere induced by cooling at such slow spreading rates. We propose the heterogeneous mantle that exists beneath Gakkel Ridge is the consequence of ancient melting, combined with subsequent melt percolation and entrapment.

Refertilization of the Subcontinental Lithospheric Mantle and its link to the formation of Metallogenic Provinces

NASA Astrophysics Data System (ADS)

Tassara, C. S.; González-Jiménez, J. M.; Reich, M.; Morata, D.; Barra, F.; Gregoire, M.; Saunders, J. E.; Cannatelli, C.

2017-12-01

Refertilisation of the subcontinental lithospheric mantle is a key process controlling the noble metal budget of the mantle, and recent views point to anomalously enriched mantle sources as a critical factor in the formation of noble metal (e.g., Au) provinces at a lithospheric scale. Here we test this hypothesis by studying peridotite xenoliths from the mantle beneath the Deseado Massif auriferous province in southern Patagonia, Argentina. Extensive Neogene back-arc plateau magmatism composed of alkaline basalts ( 3.5 Ma) has brought to the surface deep-seated mantle xenoliths from beneath the crust that host the Au mineralization. In the studied xenolith samples we found gold particles enclosed within primary olivine and pyroxene, and embedded in a highly alkaline interstitial glass or sulphides. Detailed inspection of the sulphide hosts using FESEM reveals abundant native Au nanoparticles, which are consistent with the high Au (up to 6 ppm) obtained by LA-ICP-MS analysis of these sulphides. It is relevant to note that these sulphides also contain significant amounts of Ag (up to 163 ppm). Different generations of sulphides were identified on the basis of their chondrite-normalized PGE patterns, and they can be systematically associated with different events of melt depletion and metasomatism in the mantle. Noticeably, Cu-Pd-Pt-Au rich sulfides are associated with clinopyroxene showing typical carbonatite markers (i.e., large LREE/HREE, Zr and Hf negative anomalies) and accessory minerals such as carbonates and apatite. Still, clinopyroxene commonly has high Ti contents suggesting that a "basaltic" component was also present during the metasomatism. These results suggest that overprinting of events of melt depletion and metasomatism lead to the formation of several generations of sulfides. We propose that the Cu-Pd-Pt-Au rich sulfides may be associated with carbonated silicate melts in the mantle. Our results point to 1) a link between an enriched source of gold (and silver) in the mantle and the formation of the Deseado Massif auriferous province; and 2) carbonated silicate melt metasomatism as an important factor in the PPGE + Au refertilisation of the mantle.

Tungsten isotope evidence that mantle plumes contain no contribution from the Earth's core

NASA Astrophysics Data System (ADS)

Scherstén, Anders; Elliott, Tim; Hawkesworth, Chris; Norman, Marc

2004-01-01

Osmium isotope ratios provide important constraints on the sources of ocean-island basalts, but two very different models have been put forward to explain such data. One model interprets 187Os-enrichments in terms of a component of recycled oceanic crust within the source material. The other model infers that interaction of the mantle with the Earth's outer core produces the isotope anomalies and, as a result of coupled 186Os-187Os anomalies, put time constraints on inner-core formation. Like osmium, tungsten is a siderophile (`iron-loving') element that preferentially partitioned into the Earth's core during core formation but is also `incompatible' during mantle melting (it preferentially enters the melt phase), which makes it further depleted in the mantle. Tungsten should therefore be a sensitive tracer of core contributions in the source of mantle melts. Here we present high-precision tungsten isotope data from the same set of Hawaiian rocks used to establish the previously interpreted 186Os-187Os anomalies and on selected South African rocks, which have also been proposed to contain a core contribution. None of the samples that we have analysed have a negative tungsten isotope value, as predicted from the core-contribution model. This rules out a simple core-mantle mixing scenario and suggests that the radiogenic osmium in ocean-island basalts can better be explained by the source of such basalts containing a component of recycled crust.

Sulfide enrichment at an oceanic crust-mantle transition zone: Kane Megamullion (23°N, MAR)

NASA Astrophysics Data System (ADS)

Ciazela, Jakub; Koepke, Juergen; Dick, Henry J. B.; Botcharnikov, Roman; Muszynski, Andrzej; Lazarov, Marina; Schuth, Stephan; Pieterek, Bartosz; Kuhn, Thomas

2018-06-01

The Kane Megamullion oceanic core complex located along the Mid-Atlantic Ridge (23°30‧N, 45°20‧W) exposes lower crust and upper mantle directly on the ocean floor. We studied chalcophile elements and sulfides in the ultramafic and mafic rocks of the crust-mantle transition and the mantle underneath. We determined mineralogical and elemental composition and the Cu isotope composition of the respective sulfides along with the mineralogical and elemental composition of the respective serpentines. The rocks of the crust-mantle transition zone (i.e., plagioclase harzburgite, peridotite-gabbro contacts, and dunite) overlaid by troctolites are by one order of magnitude enriched in several chalcophile elements with respect to the spinel harzburgites of the mantle beneath. Whereas the range of Cu concentrations in spinel harzburgites is 7-69 ppm, the Cu concentrations are highly elevated in plagioclase harzburgites with a range of 90-209 ppm. The zones of the peridotite-gabbro contacts are even more enriched, exhibiting up to 305 ppm Cu and highly elevated concentrations of As, Zn, Ga, Sb and Tl. High Cu concentrations show pronounced correlation with bulk S concentrations at the crust-mantle transition zone implying an enrichment process in this horizon of the oceanic lithosphere. We interpret this enrichment as related to melt-mantle reaction, which is extensive in crust-mantle transition zones. In spite of the ubiquitous serpentinization of primary rocks, we found magmatic chalcopyrites [CuFeS2] as inclusions in plagioclase as well as associated with pentlandite [(Fe,Ni)9S8] and pyrrhotite [Fe1-xS] in polysulfide grains. These chalcopyrites show a primary magmatic δ65Cu signature ranging from -0.04 to +0.29 ‰. Other chalcopyrites have been dissolved during serpentinization. Due to the low temperature (<300 °C) of circulating fluids chalcophile metals from primary sulfides have not been mobilized and transported away but have been trapped in smaller secondary sulfides and hydroxides. Combined with the Cu deposits documented in the crust-mantle transition zones of various ophiolite complexes, our results indicate that the metal enrichment, increased sulfide modes, and potentially formation of small sulfide deposits could be expected globally along the petrological Moho.

Interactions between magma and the lithospheric mantle during Cenozoic rifting in Central Europe

NASA Astrophysics Data System (ADS)

Meyer, Romain; Elkins-Tanton, Linda T.

2010-05-01

During the Cenozoic, extensive intraplate volcanic activity occurred throughout Central Europe. Volcanic eruptions extend over France (the Massif Central), central Germany (Eifel, Vogelsberg, Rhön; Heldburg), the Czech Republic (the Eger graben) and SW Poland (Lower Silesia), a region ~1,200 km wide. The origin of this predominantly alkaline intraplate magmatism is often genetically linked to one or several mantle plumes, but there is no convincing evidence for this. We have measured Pb isotope ratios, together with major and trace elements, in a representative set of mafic to felsic igneous rocks from the intra-plate Cenozoic Rhön Mts. and the Heldburg dike swarm in order to gain insight into the melting source and petrogenetic history of these melts. Three different mafic rock types (tholeiitic basalt, alkali basalt, basanite) were distinguished based on petrography and geochemistry within the investigated areas. Except for the lherzolite-bearing phonolite from the Veste Heldburg all other evolved magmas are trachytes. REE geochemistry and calculated partial melting modeling experiments for the three mafic magma types point to different degrees of partial melting in a garnet-bearing mantle source. In addition a new version of the ternary Th-Hf-Ta diagram is presented in this study as a useful petrological tool. This diagram is not only able to define potentially involved melting source end-members (e.g. asthenosphere, sub-continental lithospheric mantle and continental crust) but also interactions between these members are illustrated. An advantage of this diagram compared to partial melting degree sensitive multi-element diagrams is that a ternary diagram is a closed system. An earlier version of this diagram has been recently used to establish the nature and extent of crust mantle melt interaction of volcanic rifted margins magmas (Meyer et al. 2009). The Th-Hf-Ta geochemistry of the investigated magmas is similar to spinel and garnet xenoliths from different continental intra-plate volcanic fields The in the Rhön Mts. and the Heldburg dike swarm tapped mantle source is characterized by an enriched Pb-isotope geology. The highest HIMU component has been measured in the lherzolite-bearing Veste Heldburg phonolite. This higher enriched Pb isotope signature compared to the mafic magmas cannot be explained by crustal contamination. Assimilation fractionation crystallization (AFC) modeling of the Heldburg phonolite allows us to petrogenetically link this melt with HIMU rich shallow mantle amphibole-bearing xenoliths. These new observations suggest that melting started in more depleted mantle segments. And that these melts interacted with more enriched metasomatic overprinted lithospheric mantle domains.

Interactions between magma and the lithospheric mantle during Cenozoic rifting in Central Europe

NASA Astrophysics Data System (ADS)

Meyer, R.; Song, X.; Elkins-Tanton, L. T.

2009-12-01

During the Cenozoic, extensive intraplate volcanic activity occurred throughout Central Europe. Volcanic eruptions extend over France (the Massif Central), central Germany (Eifel, Vogelsberg, Rhön; Heldburg), the Czech Republic (the Eger graben) and SW Poland (Lower Silesia), a region ~1,200 km wide. The origin of this predominantly alkaline intraplate magmatism is often genetically linked to one or several mantle plumes, but there is no convincing evidence for this. We have measured Pb isotope ratios, together with major and trace elements, in a representative set of mafic to felsic igneous rocks from the intra-plate Cenozoic Rhön Mts. and the Heldburg dike swarm in order to gain insight into the melting source and petrogenetic history of these melts. Three different mafic rock types (tholeiitic basalt, alkali basalt, basanite) were distinguished based on petrography and geochemistry within the investigated areas. Except for the lherzolite-bearing phonolite from the Veste Heldburg all other evolved magmas are trachytes. REE geochemistry and calculated partial melting modeling experiments for the three mafic magma types point to different degrees of partial melting in a garnet-bearing mantle source. In addition a new version of the ternary Th-Hf-Ta diagram is presented in this study as a useful petrological tool. This diagram is not only able to define potentially involved melting source end-members (e.g. asthenosphere, sub-continental lithospheric mantle and continental crust) but also interactions between these members are illustrated. An advantage of this diagram compared to partial melting degree sensitive multi-element diagrams is that a ternary diagram is a closed system. An earlier version of this diagram has been recently used to establish the nature and extent of crust mantle melt interaction of volcanic rifted margins magmas (Meyer et al. 2009). The Th-Hf-Ta geochemistry of the investigated magmas is similar to spinel and garnet xenoliths from different continental intra-plate volcanic fields The in the Rhön Mts. and the Heldburg dike swarm tapped mantle source is characterized by an enriched Pb-isotope geology. The highest HIMU component has been measured in the lherzolite-bearing Veste Heldburg phonolite. This higher enriched Pb isotope signature compared to the mafic magmas cannot be explained by crustal contamination. Assimilation fractionation crystallization (AFC) modeling of the Heldburg phonolite allows us to petrogenetically link this melt with HIMU rich shallow mantle amphibole-bearing xenoliths. These new observations suggest that melting started in more depleted mantle segments. And that these melts interacted with more enriched metasomatic overprinted lithospheric mantle domains.

Geochemical and isotopic investigation of the Laiwu-Zibo carbonatites from western Shandong Province, China, and implications for their petrogenesis and enriched mantle source

NASA Astrophysics Data System (ADS)

Ying, Jifeng; Zhou, Xinhua; Zhang, Hongfu

2004-08-01

Major and trace element and Nd-Sr isotope data of the Mesozoic Laiwu-Zibo carbonatites (LZCs) from western Shandong Province, China, provide clues to the petrogenesis and the nature of their mantle source. The Laiwu-Zibo carbonatites can be petrologically classified as calcio-, magnesio- and ferro-carbonatites. All these carbonatites show a similarity in geochemistry. On the one hand, they are extremely enriched in Ba, Sr and LREE and markedly low in K, Rb and Ti, which are similar to those global carbonatites, on the other hand, they have extremely high initial 87Sr/ 86Sr (0.7095-0.7106) and very low ɛNd (-18.2 to -14.3), a character completely different from those global carbonatites. The small variations in Sr and Nd isotopic ratios suggest that crustal contamination can not modify the primary isotopic compositions of LZC magmas and those values are representatives of their mantle source. The Nd-Sr isotopic compositions of LZCs and their similarity to those of Mesozoic Fangcheng basalts imply that they derived from an enriched lithospheric mantle. The formation of such enriched lithospheric mantle is connected with the major collision between the North China Craton (NCC) and the Yangtze Craton. Crustal materials from the Yangtze Craton were subducted beneath the NCC and melts derived from the subducted crust of the Yangtze Craton produced an enriched Mesozoic mantle, which is the source for the LZCs and Fangcheng basalts. The absence of alkaline silicate rocks, which are usually associated with carbonatites suggest that the LZCs originated from the mantle by directly partial melting.

DUPAL anomaly in the Sea of Japan: Pb, Nd, and Sr isotopic variations at the eastern Eurasian continental margin

USGS Publications Warehouse

Tatsumoto, M.; Nakamura, Y.

1991-01-01

Volcanic rocks from the eastern Eurasian plate margin (southwestern Japan, the Sea of Japan, and northeastern China) show enriched (EMI) component signatures. Volcanic rocks from the Ulreung and Dog Islands in the Sea of Japan show typical DUPAL anomaly characteristics with extremely high ??208/204 Pb (up to 143) and enriched Nd and Sr isotopic compositions (??{lunate}Nd = -3 to -5, 87Sr 86Sr = ~0.705). The ??208/204 Pb values are similar to those associated with the DUPAL anomaly (up to 140) in the southern hemisphere. Because the EMI characteristics of basalts from the Sea of Japan are more extreme than those of southwestern Japan and inland China basalts, we propose that old mantle lithosphere was metasomatized early (prior to the Proterozoic) with subduction-related fluids (not present subduction system) so that it has been slightly enriched in incompatible elements and has had a high Th/U for a long time. The results of this study support the idea that the old subcontinental mantle lithosphere is the source for EMI of oceanic basalts, and that EMI does not need to be stored at the core/ mantle boundary layer for a long time. Dredged samples from seamounts and knolls from the Yamato Basin Ridge in the Sea of Japan show similar isotopic characteristics to basalts from the Mariana arc, supporting the idea that the Yamato Basin Ridge is a spreading center causing separation of the northeast Japan Arc from Eurasia. ?? 1991.

The Isotopic Record From Monogenetic Seamounts: Insights Into Recycling Time Scales In The Upper Mantle

NASA Astrophysics Data System (ADS)

Madrigal Quesada, P.; Gazel, E.

2017-12-01

Monogenetic seamounts related to non-plume intraplate magmatism provide a window into the composition of upper mantle heterogeneities, nevertheless, the origin of these heterogeneities are still not well constrained. Radiogenic isotopes (Sr-Nd-Pb) from present-day ocean island basalts (OIB) produced by this type of magmatism can help establish the source compositions of these chemically and isotopically enriched reservoirs. Here we present evidence that suggests that a highly enriched mantle reservoir can originate from OIB-type subducted material that gets incorporated and stirred throughout the upper mantle. We explore this hypothesis using data from non-plume related OIB volcanism; focusing on isolated monogenetic seamounts with no apparent age progression and interpreted to be related to either plate flexure, shear driven convection and/or edge convection. The isotopic record compiled, added to new results obtained from accreted petit-spot seamounts from Santa Elena Peninsula in Costa Rica, suggest that a highly radiogenic mantle reservoir originated from recycled seamount materials can be formed in a shorter time scale than ancient subducted oceanic crust (>1 Ga), thought to be the forming agent of the HIMU mantle "flavor" found in some of these small-scale seamounts. The implications of these results entail that the recycling of already enriched materials in short time scales and in restricted depths within the Upper Mantle may play an important role in the source of OIBs (plume and non-plume related), as well as, the most enriched suites of EMORBs.

Origin of enormous trace metal enrichments in weathering mantles of Jurassic carbonates: evidence from Sr, Nd and Pb isotopes

NASA Astrophysics Data System (ADS)

Hissler, C.; Stille, P.; Juilleret, J.; Iffly, J.; Perrone, T.; Morvan, G.

2013-12-01

Weathering mantels are widespread worldwide and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved carbonate rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual content of associated trace elements in this type of weathering mantle. For instance, these enrichments can represent about five times the content of the underlying Bajocian to Oxfordian limestone/marl complexes, which have been relatively poorly studied compared to weathering mantle developed on magmatic bedrocks. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources (saprolite, Bajocian silty marls and limestones, atmospheric particles deposition...). Of special interest has also been the origin of trace metals and the processes causing their enrichments. Especially Rare Earth Element (REE) distribution patterns and Sr, Nd and Pb isotope ratios are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments shall help to identify mobile phases in the soil system. This may inform on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. Trace metal migration and enrichments were studied on a cambisol developing on an underlying Jurassic limestone. The base is strongly enriched among others in rare earth elements (ΣREE: 2640ppm) or redox-sensitive elements such as Fe (44 wt.%), V (920ppm), Cr (700ppm), Zn (550ppm), As (260ppm), Co (45ppm) and Cd (2.4ppm). The underlying limestone and marl show, compared to average world carbonates, enrichments in the same elements and trace element distribution patterns similar to the soil suggesting their close genetic relationship. Pb, Sr and Nd isotope data allow to identify three principal components in the soil: a silicate-rich phase at close to the surface, a strongly trace metal enriched component at the bottom of the soil profile and an anthropogenic, atmosphere- derived component detected in the soil leachates. The isotopic mixing curves defined by the soil samples point to the close genetic connection between upper and lowermost soil horizons. The Nd isotopic composition of the leachates of all soil horizons are in contrast to the untreated soil and residual soil samples very homogeneous suggesting that the leachable phases of the upper and lower soil horizons are genetically connected. The downward migration of the trace metals is stopped at this soil level due to the presence of important secondary calcite precipitations, smectite and Fe-oxide accumulations. Mass balance calculations indicate that the enrichment process goes along with a volume increase relative to the bottom soil horizons.

Silicon isotopes reveal recycled altered oceanic crust in the mantle sources of Ocean Island Basalts

NASA Astrophysics Data System (ADS)

Pringle, Emily A.; Moynier, Frédéric; Savage, Paul S.; Jackson, Matthew G.; Moreira, Manuel; Day, James M. D.

2016-09-01

The study of silicon (Si) isotopes in Ocean Island Basalts (OIB) has the potential to discern between different models for the origins of geochemical heterogeneities in the mantle. Relatively large (∼several per mil per atomic mass unit) Si isotope fractionation occurs in low-temperature environments during biochemical and geochemical precipitation of dissolved Si, where the precipitate is preferentially enriched in the lighter isotopes relative to the dissolved Si. In contrast, only a limited range (∼tenths of a per mil) of Si isotope fractionation has been observed from high-temperature igneous processes. Therefore, Si isotopes may be useful as tracers for the presence of crustal material within OIB mantle source regions that experienced relatively low-temperature surface processes in a manner similar to other stable isotope systems, such as oxygen. Characterizing the isotopic composition of the mantle is also of central importance to the use of the Si isotope system as a basis for comparisons with other planetary bodies (e.g., Moon, Mars, asteroids). Here we present the first comprehensive suite of high-precision Si isotope data obtained by MC-ICP-MS for a diverse suite of OIB. Samples originate from ocean islands in the Pacific, Atlantic, and Indian Ocean basins and include representative end-members for the EM-1, EM-2, and HIMU mantle components. On average, δ30Si values for OIB (-0.32 ± 0.09‰, 2 sd) are in general agreement with previous estimates for the δ30Si value of Bulk Silicate Earth (-0.29 ± 0.07‰, 2 sd; Savage et al., 2014). Nonetheless, some small systematic variations are present; specifically, most HIMU-type (Mangaia; Cape Verde; La Palma, Canary Islands) and Iceland OIB are enriched in the lighter isotopes of Si (δ30Si values lower than MORB), consistent with recycled altered oceanic crust and lithospheric mantle in their mantle sources.

Heterogeneous source components of intraplate basalts from NE China induced by the ongoing Pacific slab subduction

NASA Astrophysics Data System (ADS)

Chen, Huan; Xia, Qun-Ke; Ingrin, Jannick; Deloule, Etienne; Bi, Yao

2017-02-01

The subduction of oceanic slabs is widely accepted to be a main reason for chemical heterogeneities in the mantle. However, determining the contributions of slabs in areas that have experienced multiple subduction events is often difficult due to possible overlapping imprints. Understanding the temporal and spatial variations of source components for widespread intraplate small volume basalts in eastern China may be a basis for investigating the influence of the subducted Pacific slab, which has long been postulated but never confirmed. For this purpose, we investigated the Chaihe-aershan volcanic field (including more than 35 small-volume Quaternary basaltic volcanoes) in NE China and measured the oxygen isotopes and water content of clinopyroxene (cpx) phenocrysts using secondary ion mass spectrometry (SIMS) and Fourier transform infrared spectroscopy (FTIR), respectively. The water content of magma was then estimated based on the partition coefficient of H2O between cpx and the basaltic melt. The δ18O of cpx phenocrysts (4.28‰ to 8.57‰) and H2O content of magmas (0.19 wt.%-2.70 wt.%) show large variations, reflecting the compositional heterogeneity of the mantle source. The δ18O values and H2O content within individual samples also display considerable variation, suggesting the mixing of magmas and that the magma mixing occurred shortly before the eruption. The relation between the δ18O values of cpx phenocrysts and the H2O/Ce ratio, Ba/Th ratio and Eu anomaly of whole rocks demonstrates the contributions of three components to the mantle source (hydrothermally altered upper oceanic crust and marine sediments, altered lower gabbroic oceanic crust, and ambient mantle). The proportions of these three components have varied widely over time (∼1.37 Ma to ∼0.25 Ma). The Pacific slab is constantly subducted under eastern Asia and continuously transports recycled materials to the deep mantle. The temporal heterogeneity of the source components may be caused by ongoing Pacific slab subduction. Combined with other basalt localities in eastern China (Shuangliao basalts, Taihang basalts and Shangdong basalts), the contributions of recycled oceanic components in their mantle source are heterogeneous. This spatial heterogeneity of mantle sources may be induced by variable alterations and dehydration during the recycling process of the Pacific slab. Our results show that the source components of Cenozoic intraplate small-volume basalts in eastern China are temporally and spatially heterogeneous, which is likely induced by the ongoing subduction of the Pacific slab. This demonstrates that integrating the temporal variations in geochemical characteristics and tectonic history of a study region can identify the subducted oceanic plate that induced enriched components in the mantle source of intraplate basalts.

Molybdenum mobility and isotopic fractionation during subduction at the Mariana arc

NASA Astrophysics Data System (ADS)

Freymuth, Heye; Vils, Flurin; Willbold, Matthias; Taylor, Rex N.; Elliott, Tim

2015-12-01

The fate of crustal material recycled into the convecting mantle by plate tectonics is important for understanding the chemical and physical evolution of the planet. Marked isotopic variability of Mo at the Earth's surface offers the promise of providing distinctive signatures of such recycled material. However, characterisation of the behaviour of Mo during subduction is needed to assess the potential of Mo isotope ratios as tracers for global geochemical cycles. Here we present Mo isotope data for input and output components of the archetypical Mariana arc: Mariana arc lavas, sediments from ODP Sites 800, 801 and 802 near the Mariana trench and the altered mafic, oceanic crust (AOC), from ODP Site 801, together with samples of the deeper oceanic crust from ODP Site 1256. We also report new high precision Pb isotope data for the Mariana arc lavas and a dataset of Pb isotope ratios from sediments from ODP Sites 800, 801 and 802. The Mariana arc lavas are enriched in Mo compared to elements of similar incompatibility during upper mantle melting, and have distinct, isotopically heavy Mo (high 98Mo/95Mo) relative to the upper mantle, by up to 0.3 parts per thousand. In contrast, the various subducting sediment lithologies dominantly host isotopically light Mo. Coupled Pb and Mo enrichment in the Mariana arc lavas suggests a common source for these elements and we further use Pb isotopes to identify the origin of the isotopically heavy Mo. We infer that an aqueous fluid component with elevated [Mo], [Pb], high 98Mo/95Mo and unradiogenic Pb is derived from the subducting, mafic oceanic crust. Although the top few hundred metres of the subducting, mafic crust have a high 98Mo/95Mo, as a result of seawater alteration, tightly defined Pb isotope arrays of the Mariana arc lavas extrapolate to a fluid component akin to fresh Pacific mid-ocean ridge basalts. This argues against a flux dominantly derived from the highly altered, uppermost mafic crust or indeed from an Indian-like mantle wedge. Thus we infer that the Pb and Mo budgets of the fluid component are dominated by contributions from the deeper, less altered (cooler) portion of the subducting Pacific crust. The high 98Mo/95Mo of this flux is likely caused by isotopic fractionation during dehydration and fluid flow in the slab. As a result, the residual mafic crust becomes isotopically lighter than the upper mantle from which it was derived. Our results suggest that the continental crust produced by arc magmatism should have an isotopically heavy Mo composition compared to the mantle, whilst a contribution of deep recycled oceanic crust to the sources of some ocean island basalts might be evident from an isotopically light Mo signature.

Re — Os isotopic constraints on the origin of volcanic rocks, Gorgona Island, Colombia: Os isotopic evidence for ancient heterogeneities in the mantle

NASA Astrophysics Data System (ADS)

Walker, R. J.; Echeverria, L. M.; Shirey, S. B.; Horan, M. F.

1991-04-01

The Re — Os isotopic systematics of komatiites and spatially associated basalts from Gorgona Island, Colombia, indicate that they were produced at 155±43 Ma. Subsequent episodes of volcanism produced basalts at 88.1±3.8 Ma and picritic and basaltic lavas at ca. 58 Ma. The age for the ultramafic rocks is important because it coincides with the late-Jurassic, early-Cretaceous disassembly of Pangea, when the North- and South-American plates began to pull apart. Deep-seated mantle upwelling possibly precipitated the break-up of these continental plates and caused a tear in the subducting slab west of Gorgona, providing a rare, late-Phanerozoic conduit for the komatiitic melts. Mantle sources for the komatiites were heterogeneous with respect to Os and Pb isotopic compositions, but had homogeneous Nd isotopic compositions (ɛNd+9±1). Initial 187Os/186Os normalized to carbonaceous chondrites at 155 Ma (γOs) ranged from 0 to +22, and model-initial μ values ranged from 8.17 to 8.39. The excess radiogenic Os, compared with an assumed bulk-mantle evolution similar to carbonaceous chondrites, was likely produced in portions of the mantle with long-term elevated Re concentrations. The Os, Pb and Nd isotopic compositions, together with major-element constraints, suggest that the sources of the komatiites were enriched more than 1 Ga ago by low (<20%) and variable amounts of a basalt or komatiite component. This component was added as either subducted oceanic crust or melt derived from greater depths in the mantle. These results suggest that the Re — Os isotope system may be a highly sensitive indicator of the presence of ancient subducted oceanic crust in mantle-source regions.

Re - Os isotopic constraints on the origin of volcanic rocks, Gorgona Island, Colombia: Os isotopic evidence for ancient heterogeneities in the mantle

USGS Publications Warehouse

Walker, R.J.; Echeverria, L.M.; Shirey, S.B.; Horan, M.F.

1991-01-01

The Re - Os isotopic systematics of komatiites and spatially associated basalts from Gorgona Island, Colombia, indicate that they were produced at 155??43 Ma. Subsequent episodes of volcanism produced basalts at 88.1??3.8 Ma and picritic and basaltic lavas at ca. 58 Ma. The age for the ultramafic rocks is important because it coincides with the late-Jurassic, early-Cretaceous disassembly of Pangea, when the North- and South-American plates began to pull apart. Deep-seated mantle upwelling possibly precipitated the break-up of these continental plates and caused a tear in the subducting slab west of Gorgona, providing a rare, late-Phanerozoic conduit for the komatiitic melts. Mantle sources for the komatiites were heterogeneous with respect to Os and Pb isotopic compositions, but had homogeneous Nd isotopic compositions (??Nd+9??1). Initial 187Os/186Os normalized to carbonaceous chondrites at 155 Ma (??Os) ranged from 0 to +22, and model-initial ?? values ranged from 8.17 to 8.39. The excess radiogenic Os, compared with an assumed bulk-mantle evolution similar to carbonaceous chondrites, was likely produced in portions of the mantle with long-term elevated Re concentrations. The Os, Pb and Nd isotopic compositions, together with major-element constraints, suggest that the sources of the komatiites were enriched more than 1 Ga ago by low (<20%) and variable amounts of a basalt or komatiite component. This component was added as either subducted oceanic crust or melt derived from greater depths in the mantle. These results suggest that the Re - Os isotope system may be a highly sensitive indicator of the presence of ancient subducted oceanic crust in mantle-source regions. ?? 1991 Springer-Verlag.

Petrogenesis of a Mesoproterozoic shoshonitic lamprophyre dyke from the Wajrakarur kimberlite field, eastern Dharwar craton, southern India: Geochemical and Sr-Nd isotopic evidence for a modified sub-continental lithospheric mantle source

NASA Astrophysics Data System (ADS)

Pandey, Ashutosh; Chalapathi Rao, N. V.; Chakrabarti, Ramananda; Pandit, Dinesh; Pankaj, Praveer; Kumar, Alok; Sahoo, Samarendra

2017-11-01

Mineralogy and geochemistry of the Udirpikonda lamprophyre, located within the Mesoproterozoic diamondiferous Wajrakarur kimberlite field (WKF), towards the western margin of the Paleo-Mesoproterozoic Cuddapah basin are presented. The lamprophyre is characterised by a panidiomorphic-porphyritic texture imparted by clinopyroxene, olivine and biotite set in a groundmass of feldspar and spinel. Olivine occurs as the microphenocrysts with a composition range of Fo87-78. Clinopyroxenes display reverse as well as oscillatory optical zoning and are diopsidic in nature with a variation in the composition from core (Wo47 En28 Fs20Ac5) to rim (Wo46En41Fs11Ac3). Biotite (Mg# < 0.6) is the only mica present and spinels are titano-magnetites showing ulvospinel- magnetite solid solution. Plagioclase is the dominant feldspar with a variable compositional range of An41-8Ab82-56Or33-3. Based on the mineralogy, the lamprophyre can be classified to be of calc-alkaline variety but its geochemistry display mixed signals of both alkaline and calc-alkaline lamprophyres. K2O/Na2O ranges from 1.49 to 2.79, making it distinctly potassic and highlights its shoshonitic character. Moderate Mg# (60-65), Ni (110-200 ppm) and Cr (110-260 ppm) contents in the bulk-rock indicate substantial fractional crystallization of olivine and clinopyroxene. Fractionated chondrite normalized REE patterns (average (La/Yb)N = 37.56) indicates involvement of an enriched mantle source from within the garnet stability field whereas slightly negative Ta-Nb-Ti and Hf anomalies displayed on the primitive mantle normalized multi-element spider gram highlight involvement of a subducted component in the mantle source. Given the spatial disposition of the studied lamprophyre, the age of the emplacement is considered to be coeval with WKF kimberlites ( 1.1 Ga) and the initial 143Nd/144Nd (0.510065-0.510192) and 87Sr/86Sr (0.705333-0.706223) are strikingly similar to those observed for the Smoky Butte lamproites, Montana, USA. Fluid-related subduction enrichment of the mantle source is apparent from the enriched ratios of La/Nb, Ba/Nb and (Hf/Sm)N, (Ta/La)N < 1. Petrogenetic modelling reveals melt generation from 1 to 2% partial melting of an enriched mantle source that subsequently underwent fractional crystallization. Our study provides geochemical and isotopic evidence for a sub-continental lithospheric mantle (SCLM) modified by subduction and asthenospheric upwelling in the Eastern Dharwar Craton. The partial melting of a resulting heterogeneous Eastern Dharwar Craton SCLM to generate Udiripikonda lamprophyre and Wajrakarur kimberlites has been attributed to the Mesoproterozoic regional lithospheric extension event.

Hf and Nd Isotope Evidence for Production of an Incompatible Trace Element Enriched Crustal Reservoir in Early Earth (Invited)

NASA Astrophysics Data System (ADS)

Brandon, A. D.; Debaille, V.; Lapen, T. J.

2010-12-01

The final significant stage of accretion of the Earth was likely a collision between proto-Earth and a Mars sized impactor that formed the Moon. This event is thought to have produced enough thermal energy to melt all or most of the Earth, with a consequent magma ocean (MO). During subsequent cooling, the Earth would have formed its protocrust and corresponding mantle lithosphere, consisting of solidified basalt-komatiitic melt, in combination with buoyant cumulates and late stage residual melts from the MO. Relative to the convecting mantle, portions of this protolithosphere are likely to have been enriched in incompatible trace elements (ITE) in sufficient quantities to contain a significant amount of the bulk Earth’s budget for rare earth elements, U, Th, and Hf. If the protolithosphere was negatively buoyant, it may have overturned at or near the final stages of MO crystallization and a significant portion of that material may have been transported into the deep mantle where it resided and remixed into the convecting mantle over Earth history [1,2]. If the protolithosphere remained positively buoyant, its crust would have likely begun to erode from surface processes, and subsequently recycled back into the mantle over time as sediment and altered crust, once a subduction mechanism arose. The Nd and Hf isotopic compositions of Earth’s earliest rocks support the idea that an early-formed ITE-enriched reservoir was produced. The maxima in 142Nd/144Nd for 3.85 to 3.64 Ga rocks from Isua, Greenland decreases from +20 ppm to +12 ppm relative to the present day mantle value, respectively [3]. This indicates mixing of an early-formed ITE enriched reservoir back into the convecting mantle. In addition, zircons from the 3.1 Ga Jack Hills conglomerate indicate that material with an enriched 176Lu/177Hf of ~0.02 and an age of 4.4 Ga or greater was present at the Earth’s surface over the first 2 Ga of Earth history, supporting the scenario of a positively buoyant, early-formed ITE-enriched reservoir [4]. This early-formed enriched ITE reservoir is indistinguishable in age and 176Lu/177Hf to those that formed in the Moon and Mars [5,6]. Hence all three terrestrial bodies must have undergone similar early differentiation and each formed and sustained their requisite early-formed ITE-enriched reservoirs at or near their surfaces. For all three terrestrial bodies, their early-formed ITE-enriched reservoirs appear to be the result of solidification of late stage residual liquids from their respective MO’s at or prior to 4.4 Ga. In Earth, mixing of an early-formed ITE-enriched reservoir back into the mantle likely occurred back into the convecting mantle at or before 3.9 Ga. For the Moon and Mars, the lack of plate tectonics preserved their early-formed ITE-enriched lithospheric reservoirs. [1] Tolstikhin and Hofmann, PEPI (2005) 148, 109. [2] Boyet and Carlson, Science (2005) 309, 576. [3] Bennett et al., Science (2007) 218, 1907. [3] Kemp et al., EPSL (2010) 296, 45. [5] Taylor et al. (2009) 279, 157. [6] Lapen et al., Science (2010) 328, 347.

Slab melting and magma formation beneath the southern Cascade arc

USGS Publications Warehouse

Walowski, Kristina J.; Wallace, Paul J.; Clynne, Michael A.; Rasmussen, D.J.; Weis, D.

2016-01-01

The processes that drive magma formation beneath the Cascade arc and other warm-slab subduction zones have been debated because young oceanic crust is predicted to largely dehydrate beneath the forearc during subduction. In addition, geochemical variability along strike in the Cascades has led to contrasting interpretations about the role of volatiles in magma generation. Here, we focus on the Lassen segment of the Cascade arc, where previous work has demonstrated across-arc geochemical variations related to subduction enrichment, and H-isotope data suggest that H2O in basaltic magmas is derived from the final breakdown of chlorite in the mantle portion of the slab. We use naturally glassy, olivine-hosted melt inclusions (MI) from the tephra deposits of eight primitive (MgO>7 wt%) basaltic cinder cones to quantify the pre-eruptive volatile contents of mantle-derived melts in this region. The melt inclusions have B concentrations and isotope ratios that are similar to mid-ocean ridge basalt (MORB), suggesting extensive dehydration of the downgoing plate prior to reaching sub-arc depths and little input of slab-derived B into the mantle wedge. However, correlations of volatile and trace element ratios (H2O/Ce, Cl/Nb, Sr/Nd) in the melt inclusions demonstrate that geochemical variability is the result of variable addition of a hydrous subduction component to the mantle wedge. Furthermore, correlations between subduction component tracers and radiogenic isotope ratios show that the subduction component has less radiogenic Sr and Pb than the Lassen sub-arc mantle, which can be explained by melting of subducted Gorda MORB beneath the arc. Agreement between pMELTS melting models and melt inclusion volatile, major, and trace element data suggests that hydrous slab melt addition to the mantle wedge can produce the range in primitive compositions erupted in the Lassen region. Our results provide further evidence that chlorite-derived fluids from the mantle portion of the slab (∼7–9 km below the slab top) cause flux melting of the subducted oceanic crust, producing hydrous slab melts that migrate into the overlying mantle, where they react with peridotite to induce further melting.

Platinum-group element contents of Karelian kimberlites: Implications for the PGE budget of the sub-continental lithospheric mantle

NASA Astrophysics Data System (ADS)

Maier, W. D.; O'Brien, H.; Peltonen, P.; Barnes, Sarah-Jane

2017-11-01

We present high-precision isotope dilution data for Os, Ir, Ru, Pt, Pd and Re in Group I and Group II kimberlites from the Karelian craton, as well as 2 samples of the Premier Group I kimberlite pipe from the Kaapvaal craton. The samples have, on average, 1.38 ppb Pt and 1.33 ppb Pd, with Pt/Pd around unity. These PGE levels are markedly lower, by as much as 80%, than those reported previously for kimberlites from South Africa, Brazil and India, but overlap with PGE results reported recently from Canadian kimberlites. Primitive-mantle-normalised chalcophile element patterns are relatively flat from Os to Pt, but Cu, Ni and, somewhat less so, Au are enriched relative to the PGE (e.g., Cu/Pd > 25.000). Pd/Ir ratios are 3,6 on average, lower than in most other mantle melts. The PGE systematics can be largely explained by two components, (i) harzburgite/lherzolite detritus of the SCLM with relatively high IPGE (Os-Ir-Ru)/PPGE (Rh-Pt-Pd) ratios, and (ii) a melt component that has high PPGE/IPGE ratios. By using the concentrations of iridium in the kimberlites as a proxy for the proportion of mantle detritus in the magma, we estimate that the analysed kimberlites contain 3-27% entrained and partially dissolved detritus from the sub-continental lithospheric mantle, consistent with previous estimates of kimberlites elsewhere (Tappe S. et al., 2016, Chem. Geol. 10.1016/j.chemgeo.2016.08.019).

Ultramafic xenoliths from the Bearpaw Mountains, Montana, USA: Evidence for multiple metasomatic events in the lithospheric mantle beneath the Wyoming craton

USGS Publications Warehouse

Downes, H.; Macdonald, R.; Upton, B.G.J.; Cox, K.G.; Bodinier, J.-L.; Mason, P.R.D.; James, D.; Hill, P.G.; Hearn, B.C.

2004-01-01

Ultramafic xenoliths in Eocene minettes of the Bearpaw Mountains volcanic field (Montana, USA), derived from the lower lithosphere of the Wyoming craton, can be divided based on textural criteria into tectonite and cumulate groups. The tectonites consist of strongly depleted spinel lherzolites, harzbugites and dunites. Although their mineralogical compositions are generally similar to those of spinel peridotites in off-craton settings, some contain pyroxenes and spinels that have unusually low Al2O3 contents more akin to those found in cratonic spinel peridotites. Furthermore, the tectonite peridotites have whole-rock major element compositions that tend to be significantly more depleted than non-cratonic mantle spinel peridotites (high MgO, low CaO, Al2O3 and TiO2) and resemble those of cratonic mantle. These compositions could have been generated by up to 30% partial melting of an undepleted mantle source. Petrographic evidence suggests that the mantle beneath the Wyoming craton was re-enriched in three ways: (1) by silicate melts that formed mica websterite and clinopyroxenite veins; (2) by growth of phlogopite from K-rich hydrous fluids; (3) by interaction with aqueous fluids to form orthopyroxene porphyroblasts and orthopyroxenite veins. In contrast to their depleted major element compositions, the tectonite peridotites are mostly light rare earth element (LREE)-enriched and show enrichment in fluid-mobile elements such as Cs, Rb, U and Pb on mantle-normalized diagrams. Lack of enrichment in high field strength elements (HFSE; e.g. Nb, Ta, Zr and Hf) suggests that the tectonite peridotites have been metasomatized by a subduction-related fluid. Clinopyroxenes from the tectonite peridotites have distinct U-shaped REE patterns with strong LREE enrichment. They have 143Nd/144Nd values that range from 0??5121 (close to the host minette values) to 0??5107, similar to those of xenoliths from the nearby Highwood Mountains. Foliated mica websterites also have low 143Nd/144Nd values (0??5113) and extremely high 87Sr/86Sr ratios in their constituent phlogopite, indicating an ancient (probably mid-Proterozoic) enrichment. This enriched mantle lithosphere later contributed to the formation of the high-K Eocene host magmas. The cumulate group ranges from clinopyroxene-rich mica peridotites (including abundant mica wehrlites) to mica clinopyroxenites. Most contain >30% phlogopite. Their mineral compositions are similar to those of phenocrysts in the host minettes. Their whole-rock compositions are generally poorer in MgO but richer in incompatible trace elements than those of the tectonite peridotites. Whole-rock trace element patterns are enriched in large ion lithophile elements (LILE; Rb, Cs, U and Pb) and depleted in HFSE (Nb, Ta Zr and Hf as in the host minettes, and their Sr-Nd isotopic compositions are also identical to those of the minettes. Their clinopyroxenes are LREE-enriched and formed in equilibrium with a LREE-enriched melt closely resembling the minettes. The cumulates therefore represent a much younger magmatic event, related to crystallization at mantle depths of minette magmas in Eocene times, that caused further metasomatic enrichment of the lithosphere. ?? Oxford University Press 2004; all rights reserved.

Petrogenesis and tectonic implications of Triassic mafic complexes with MORB/OIB affinities from the western Garzê-Litang ophiolitic mélange, central Tibetan Plateau

NASA Astrophysics Data System (ADS)

Liu, Bin; Ma, Chang-Qian; Guo, Yu-Heng; Xiong, Fu-Hao; Guo, Pan; Zhang, Xin

2016-09-01

Although numerous Paleo-Tethyan ophiolites with mid-oceanic ridge basalts (MORB) and/or oceanic-island basalt (OIB) affinities have been reported in the central Tibetan Plateau (CTP), the origin and tectonic nature of these ophiolites are not well understood. The petrogenesis, mantle sources and geodynamic setting of the mafic rocks from these ophiolites are unclear, which is the main reason for this uncertainty. In this paper, we present new geochronological, mineralogical and Sr-Nd isotopic data for the Chayong and Xiewu mafic complexes in the western Garzê-Litang suture zone (GLS), a typical Paleo-Tethyan suture crossing the CTP. Zircon LA-ICP-MS U-Pb ages of 234 ± 3 Ma and 236 ± 2 Ma can be interpreted as formation times of the Chayong and Xiewu mafic complexes, respectively. The basalts and gabbros of the Chayong complex exhibit enriched MORB (E-MORB) compositional affinities except for a weak depletion of Nb, Ta and Ti relative to the primitive mantle, whereas the basalts and gabbros of the Xiewu complex display distinct E-MORB and OIB affinities. The geochemical features suggest a probable fractionation of olivine ± clinopyroxene ± plagioclase as well as insignificant crustal contamination. The geochemical and Sr-Nd isotopic data reveal that the Chayong mafic rocks may have been derived from depleted MORB-type mantle metasomatized by crustal components and Xiewu mafic rocks from enriched lithospheric mantle metasomatized by OIB-like components. The ratios of Zn/Fet, La/Yb and Sm/Yb indicate that these mafic melts were produced by the partial melting of garnet + minor spinel-bearing peridotite or spinel ± minor garnet-bearing peridotite. We propose that back-arc basin spreading associated with OIB/seamount recycling had occurred in the western GLS at least since the Middle Triassic times, and the decompression melting of the depleted MORB-type asthenosphere mantle and partial melting of sub-continental lithosphere were metasomatized by plume-related melts, such as OIB s, which led to the generation of the Chayong and Xiewu mafic melts.

Stretching and smearing of chemical heterogeneity by melting and melt migration beneath mid-ocean ridges

NASA Astrophysics Data System (ADS)

Liu, B.; Liang, Y.

2017-12-01

The size of mantle source heterogeneity is important to the interpretation of isotopic signals observed in residual peridotites and basalts. During concurrent melting and melt migration beneath a mid-ocean ridge, both porosity and melt velocity increase upward, resulting in an upward increase in the effective transport velocity for a trace element. Hence a chemical heterogeneity of finite size will be stretched during its transport in the upwelling mantle. This melt migration induced chemical deformation can be quantified by a simple stretching factor. During equilibrium melting, the isotope signals of Sr, Nd and Hf in a 1 km size enriched mantle will be stretched to 2 6 km at the top of the melting column, depending on the style of melt migration. A finite rate of diffusive exchange between residual minerals and partial melt will result in smearing of chemical heterogeneity during its transport in the upwelling melting column. A Gaussian-shaped enriched source in depleted background mantle would be gradually deformed its transit through the melting column. The width of the enriched signal spreads out between the fronts of melt and solid while its amplitude decreases. This melt migration induced smearing also cause mixing of nearby heterogeneities or absorption of enriched heterogeneity by the ambient mantle. Smaller heterogeneities in the solid is more efficiently mixed or aborted by the background mantle than larger ones. Mixing of heterogeneities in the melt depends on the size in the same sense although the erupted melt is more homogenized due to melt accumulation and magma chamber process. The mapping of chemical heterogeneities observed in residual peridotites and basalts into their source region is therefore highly nonlinear. We will show that the observed variations in Nd and Hf isotopes in the global MORB and abyssal peridotites are consistent with kilometer-scale enriched heterogeneities embedded in depleted MORB mantle.

Tidal tomography constrains Earth's deep-mantle buoyancy.

PubMed

Lau, Harriet C P; Mitrovica, Jerry X; Davis, James L; Tromp, Jeroen; Yang, Hsin-Ying; Al-Attar, David

2017-11-15

Earth's body tide-also known as the solid Earth tide, the displacement of the solid Earth's surface caused by gravitational forces from the Moon and the Sun-is sensitive to the density of the two Large Low Shear Velocity Provinces (LLSVPs) beneath Africa and the Pacific. These massive regions extend approximately 1,000 kilometres upward from the base of the mantle and their buoyancy remains actively debated within the geophysical community. Here we use tidal tomography to constrain Earth's deep-mantle buoyancy derived from Global Positioning System (GPS)-based measurements of semi-diurnal body tide deformation. Using a probabilistic approach, we show that across the bottom two-thirds of the two LLSVPs the mean density is about 0.5 per cent higher than the average mantle density across this depth range (that is, its mean buoyancy is minus 0.5 per cent), although this anomaly may be concentrated towards the very base of the mantle. We conclude that the buoyancy of these structures is dominated by the enrichment of high-density chemical components, probably related to subducted oceanic plates or primordial material associated with Earth's formation. Because the dynamics of the mantle is driven by density variations, our result has important dynamical implications for the stability of the LLSVPs and the long-term evolution of the Earth system.

Mantle helium in ground waters of eastern North America: Time and space constraints on sources

USGS Publications Warehouse

Torgersen, T.; Drenkard, S.; Stute, M.; Schlosser, P.; Shapiro, A.

1995-01-01

Mantle helium in continental environments is generally considered to be the result of active volcanism and/or active extension. The latest episodes of volcanism in northeastern North America are the track of the New England hotspot (95–190 Ma) and the closure of the Iapetus sea (before 300 Ma). Thus, the identification of mantle helium in young ground waters of central New England is counter to the conventional wisdom. On the basis of evaluation of helium evolution in emplaced magmas, we postulate an “aged” mantle source for the excess helium component in ground waters of central New England that is either (1) a local, near-surface–emplaced, gas-rich magma that has retained significant volatiles (e.g., in fluid inclusions) or (2) a deeply emplaced gas-rich magma with high initial 2He/4He (10−5) and helium transport (with dispersion) through the crust over time. This gas-rich initial condition may support the concept of a volatile-enriched mantle wedge and thus explain the increased buoyancy flux of the New England hotspot as it traversed eastern North America, as has been suggested by others.

187Os-enriched domain in an Archean mantle plume: evidence from 2.8 Ga komatiites of the Kostomuksha greenstone belt, NW Baltic Shield

NASA Astrophysics Data System (ADS)

Puchtel, Igor S.; Brügmann, Gerhard E.; Hofmann, Albrecht W.

2001-04-01

The Re-Os data on Archean komatiites from the Kostomuksha greenstone belt in the Baltic Shield are presented. This greenstone belt has been previously interpreted to represent a former oceanic plateau formed by the emplacement of an ancient plume head [Puchtel et al., Earth Planet. Sci. Lett. 155 (1998) 57-74]. Samples of flowtop breccia, spinifex-textured and cumulate komatiites and a chromite separate, all collected from the core of a 300 m deep diamond drill hole, yielded a Re-Os isochron with an age of 2795±40 Ma and an initial 187Os/188Os of 0.1117±0.0011 (γ187Os=+3.6±1.0). The high positive γ187Os(T) implies that the komatiites were derived from a mantle source with a time-integrated suprachondritic Re/Os ratio. Recycling of oceanic lithosphere to produce the enriched 187Os isotope signature is considered unlikely, as 15-25% crustal component is required to be incorporated into the plume source as early as 3.5-4.3 Ga. Such a substantial proportion of mafic material in the source would likely destroy the major and trace element characteristics of the komatiites. Our tentative interpretation is that the 187Os-enrichment in the Kostomuksha plume represents an outer core signature. If confirmed by the ongoing Pt-Os isotope studies, the results would provide evidence for the existence of whole-mantle convection in the late Archean, and might place constraints on the timing of core differentiation in the early Earth.

The Feedback Between Continents and Compositional Anomalies in the Deep Mantle

NASA Astrophysics Data System (ADS)

Lowman, J. P.; Trim, S. J.

2014-12-01

Findings from global seismic tomography studies suggest that the deep mantle may harbor a pair of broad, steep-sided, relatively dense compositionally anomalous provinces. The longevity and stability of these Large Low Shear-Wave Velocity Provinces (LLSVPs) has received considerable interest but their possible influence on surface motion has drawn lesser attention. Recent work using numerical mantle convection models investigated the feedback between oceanic plate motion and high density compositional anomalies. It was found that surface mobility is affected by the presence of compositional anomalies such that critical density contrasts and volumes of the enriched material produce a transition to stagnant-lid convection. For lesser volumes and density contrast (for example, volumes that are representative of the concentrations in the Earth's mantle) the presence of the compositional anomalies affects mean plate velocity and size when compared to the characteristics of systems in which the enriched material is absent. In addition, numerous studies and lines of evidence in the geologic record suggest that the presence of the density anomalies plays a role in determining the location of mantle upwellings, which in turn influence surface dynamics. In this study, we present the results from a study implementing a two-dimensional mantle convection model featuring an anomalously dense component and distinct continental and oceanic lithosphere. The mass, momentum, and energy conservation equations are solved using a hybrid spectral-finite difference code. Compositional variations are tracked using Lagrangian tracer particles. Mobile tectonic plates are modeled using a force-balance method and plate boundary locations evolve in response to interior stresses, plate velocity, age and lithospheric chemistry (i.e., oceanic versus continental). We examine the influence of continents on compositional anomaly morphology and longevity and the influence of compositional anomalies on continental size, mobility and aggregation. The influence of continents is isolated by comparing our calculations with cases in which continents are absent.

Evolution of the Archean Mohorovičić discontinuity from a synaccretionary 4.5 Ga protocrust

NASA Astrophysics Data System (ADS)

Hamilton, Warren B.

2013-12-01

This review evaluates and rejects the currently dominant dogmas of geodynamics and geochemistry, which are based on 1950s-1970s assumptions of a slowly differentiating Earth. Evidence is presented for evolution of mantle, crust, and early Moho that began with fractionation of most crustal components, synchronously with planetary accretion, into mafic protocrust by ~ 4.5 Ga. We know little about Hadean crustal geology (> 3.9 Ga) except that felsic rocks were then forming, but analogy with Venus, and dating from the Moon, indicate great shallow disruption by large and small impact structures, including huge fractionated impact-melt constructs, throughout that era. The mantle sample and Archean (< 3.9 Ga) crustal geology integrate well. The shallow mantle was extremely depleted by early removal of thick mafic protocrust, which was the primary source of the tonalite, trondhjemite, and granodiorite (TTG) that dominate preserved Archean crust to its base, and of the thick mafic volcanic rocks erupted on that crust. Lower TTG crust, kept mobile by its high radioactivity and by insulating upper crust, rose diapirically into the upper crust as dense volcanic rocks sagged synformally. The mobile lower crust simultaneously flowed laterally to maintain subhorizontal base and surface, and dragged overlying brittler granite-and-greenstone upper crust. Petrologically required garnet-rich residual protocrust incrementally delaminated, sank through low-density high-mantle magnesian dunite, and progressively re-enriched upper mantle, mostly metasomatically. Archean and earliest Proterozoic craton stabilization and development of final Mohos followed regionally complete early delamination of residual protocrust, variously between ~ 2.9 and 2.2 Ga. Where some protocrust remained, Proterozoic basins, filled thickly by sedimentary and volcanic rocks, developed on Archean crust, beneath which delamination of later residual protocrust continued top-down enrichment of upper mantle. That reenrichment enabled modern-style plate tectonics after ~ 600 Ma, with a transition regime beginning ~ 850 Ma.

The role of hydrothermal fluids in the production of subduction zone magmas: Evidence from siderophile and chalcophile trace elements and boron

NASA Astrophysics Data System (ADS)

Noll, P. D.; Newsom, H. E.; Leeman, W. P.; Ryan, J. G.

1996-02-01

In order to evaluate the processes responsible for the enrichments of certain siderophile/ chalcophile trace elements during the production of subduction-related magmas, representative lavas from seven subduction zones have been analyzed for Pb, As, Sb, Sn, W, Mo, Tl, Cu, and Zn by inductively coupled plasma-mass spectrometry (ICP-MS), radiochemical epithermal neutron activation analysis (RENA), and atomic absorption (AA). The siderophile/chalcophile elements are compared to the highly fluid-mobile element B, the light rare earth elements (LREEs), U, and Th in order to place constraints on their behavior in subduction zones. Boron, As, Sb, and Pb are all enriched in arc lavas and continental crustal rocks more so than expected assuming normal magmatic processes (melting and crystallization). Tin, W, and Mo show little evidence of enrichment. Correlations of Pb/Ce, As/Ce, and Sb/Ce with B/La are statistically significant and have high correlation coefficients (and, more importantly, slopes approaching one) suggesting that Pb, As, and Sb behave similarly to B (i.e., that they are fluid-mobile). In addition, across-arc traverses show that B/La, As/Ce, Pb/Ce, and Sb/Ce ratios decrease dramatically with distance towards the back-arc basin. W/Th, Tl/La, Sn/Sm, and Mo/Ce ratios and Cu and Zn concentrations have much less systematic across-arc variations and correlations with B/La are not as strong (and in some cases, not statistically significant) and the regression lines have much lower slopes. Mixing models between upper mantle, slab-derived fluid, and sediment are consistent with a fluid-derived component in the arcs displaying extra enrichments of B, Pb, As, and Sb. These observations imply efficient mobilization of B, Pb, As, Sb, and possibly Tl into arc magma source regions by hydrothermal fluids derived from metamorphic dehydration reactions within the slab. Tin, W, and Mo show little, if any, evidence of hydrothermal mobilization. Copper appears to be slightly enriched in arc lavas relative to mid-ocean ridge basalts (MORBs) whereas Zn contents of arc lavas, MORB, ocean island basalts (OIBs), and continental crustal samples are similar suggesting that the bulk partition coefficient for Zn is approximately equal to one. However, Zn contents of the upper mantle are lower than these reservoirs implying an enrichment of the source region in Zn prior to melting. These nonigneous enrichments have implications not only for arc magma genesis but also for continental crust formation and crust-mantle evolution. The mobility of Pb, As, Sb, and B in hot, reducing, acidic hydrothermal fluids may be greatly enhanced relative to the large-ion lithophile elements (LILEs; including U) as a result of HS -, H 2S, OH -, or other types of complexing. In the case of Pb, continued transport of Pb from subducted slabs into arc magma source regions throughout Earth history coupled with a U fluxing of the mantle a the end of the Archean may account for the depletion of Pb in the upper mantle, the low U/Pb of most arc volcanics and continental crustal rocks, and provide an explanation for the Pb- Paradox (Hofmann et al., 1986;McCulloch, 1993;Miller et al., 1994). Recycled slabs will then retain high U/Pb ratios upon entering the deep mantle and may eventually become incorporated into the source regions of many OIBs; some with HIMU (high 238U/ 204Pb) signatures.

Chemistry of amphiboles and clinopyroxenes from Euganean (NE Italy) cumulitic enclaves: implications for the genesis of melts in an extensional setting

NASA Astrophysics Data System (ADS)

Bartoli, O.; Meli, S.; Sassi, R.; Magaraci, D.

2009-04-01

The magmatism of the Euganean Volcanic District (Veneto Volcanic Province, VVP) developed in the last phases of the Alpine orogenesis; the geochemical and geophysical data are consistent with an extensional geodynamic context (Milani et al., 1999). Cumulitic gabbroic enclaves occur within the Euganean trachytes, and Bartoli et al. (2008) pointed to their cogenetic origin with the Euganean host lavas. Sr isotopic data suggest that these cumulates derived from uncontaminated mantle-derived liquids. We analysed both cumulus and intercumulus amphiboles and clinopyroxenes by electron microprobe and LA-ICP-MS. The cumulus-intercumulus Cpx are diopsides and augites. The Mg#Cpx varies in a wide range (Mg#cumulus-Cpx= 0.74-0.84 and Mg#intercumulus-Cpx= 0.67-0.68). They show a MREE enrichment relative to LREE and HREE (LaN/SmN= 0.46-0.68 and TbN/YbN= 2.18-4.77). No significant Eu anomaly (Eu/Eu* = 0.78-1.23) was observed. On a chondrite-normalized spiderdiagram Cpx exhibits significant Pb and Co negative anomalies, and less evident negative anomalies for Sr and Zr. La, Sm and HREE increase, whereas Ba, Ti, Li and V decrease from core to rim. These Cpx exhibit high Cr contents (701-2958 ppm). Moreover, they display trace element differences when compared to Cpx from MORB gabbros. We analyzed also amphiboles: pargasites, edenites and kaersutites. In the cumulus Amph Mg# varies in the range 0.60-0.69, whereas in the intercumulus assemblage from 0.57 to 0.63. The high K2O and TiO2 contents are distinct from that of amphiboles in MORB gabbros. LREE are enriched relative to HREE (LaN/YbN = 5.07-7.56). Moreover, TbN/YbN = 2.50-4.02 indicates a HREE depletion relative to MREE. REE patterns lack a significant Eu anomaly (Eu/Eu* = 1.06-1.19). From core to rim Th and U decrease in cumulus crystals, but they increase in the intercumulus Amph. Ba (258-282 ppm) is enriched relative to other LILE and Nb-Ta are enriched relative to LREE. Cr varies in the range 423-594 ppm. The similar REE and HFSE content of intercumulus and cumulus Amph may suggest the existence of some post-cumulus processes. We calculated the chemistry of the liquids which should have been in equilibrium with cumulus phases, employing a set of Ds•l. In the liquid in equilibrium with Cpx LREE and MREE are enriched up to 40 and 11 times respectively relative to HREE, which are at about N-MORB concentrations (LaN/YbN = 42.5 and SmN/YbN = 11). Some LILE (i.e., Rb and Ba), Th and U are enriched relative to HFSE and REE. The theoretical composition of the liquid in equilibrium with Amph differs from Cpx-liquid in the marked enrichment of U and Th over LILE and HFSE. A LREE and MREE enrichment is observed (LaN/YbN = 35.4 and SmN/YbN = 3.6). The discrepancies of calculated liquid compositions cannot be ascribed only to the uncertainty in the choice of Ds•l. This may indicate trace element modifications in response to post-cumulus processes involving the amphiboles. The concentrations of HFSE in the calculated liquids (Zr/Hf = 60.2-72.7, Zr/Nb = 1.7-6.5 and Th/Hf = 3.8-6.9) and the incompatible element ratios, (e.g., La/Nb = 0.5-0.7, Pb/Ce = 0.01-0.05, La/Y = 2.3-2.8 and Ce/Nd = 1.9-2.8), are not comparable to those of N-MORB but to those of HIMU-OIB suggesting that typical MORB-type mantle couldn't be the source of these liquids. Nb and Ta are variable, possibly due to an heterogeneity in the lithospheric mantle. The existence of some peculiar trace element signatures of the recalculated liquids (LILE enrichment, high LREE/HREE ratio and abrupt enrichment in U and Th) has been attributed to slab-derived melts/fluids with an abundant sedimentary component. Our estimates are in agreement with the geodynamic scenario proposed by Macera et al. (2007), who explained the occurrence of both HIMU-OIB-type magmatism and subduction-related metasomatism in the VVP mantle lithosphere. According to their model, a mantle plume with HIMU-OIB geochemical signature rose from the deep mantle twice with subsequent partial melting episodes of the plume material: the first time during Paleocene, before the subducted European lithospheric slab (from which the LILE-, U- and Th-enriched fluids/melts derived) intercepted the mantle plume, and the second time during middle Eocene, after slab detachment and opening of a plate window. The liquids we have modeled can derive from partial melting of a subcontinental mantle source percolated by HIMU-OIB- and subduction-related fluids/melts with an abundant sedimentary component. Similarly, our recalculated liquids display some trace element signatures close to those shown by the liquids computed by Tiepolo & Tribuzio (2005) for cumulates of the Adamello batholith during alpine orogeny.

A More Reduced Mantle Source for Enriched Shergottites; Insights from the Olivine-Phyric Shergottite Lar 06319

NASA Technical Reports Server (NTRS)

Peslier, A. H.; Hnatyshin, D.; Herd, C. D. K.; Walton, E. L.; Brandon, A. D.; Lapen, T. J.; Shafer, J.

2010-01-01

A detailed petrographic study of melt inclusions and Cr-Fe-Ti oxides of LAR 06319 leads to two main conclusions: 1) this enriched oxidized olivine- phyric shergottite represents nearly continuous crystallization of a basaltic shergottite melt, 2) the melt became more oxidized during differentiation. The first crystallized mineral assemblages record the oxygen fugacity which is closest to that of the melt s mantle source, and which is lower than generally attributed to the enriched shergottite group.

Barium isotope geochemistry of subduction-zone magmas

NASA Astrophysics Data System (ADS)

Yu, H.; Nan, X.; Huang, J.; Wörner, G.; Huang, F.

2017-12-01

Subduction zones are crucial tectonic setting to study material exchange between crust and mantle, mantle partial melting with fluid addition, and formation of ore-deposits1-3. The geochemical characteristics of arc lavas from subduction zones are different from magmas erupted at mid-ocean ridges4, because there are addition of fluids/melts from subducted AOC and its overlying sediments into their source regions in the sub-arc mantle4. Ba is highly incompatible during mantle melting5, and it is enriched in crust (456 ppm)6 relative to the mantle (7.0 ppm)7. The subducted sediments are also enriched in Ba (776 ppm of GLOSS)8. Moreover, because Ba is fluid soluble during subduction, it has been used to track contributions of subduction-related fluids to arc magmas9 or recycled sediments to the mantle10-11. To study the Ba isotope fractionation behavior during subduction process, we analyzed well-characterized, chemically-diverse arc lavas from Central American, Kamchatka, Central-Eastern Aleutian, and Southern Lesser Antilles. The δ137/134Ba of Central American arc lavas range from -0.13 to 0.24‰, and have larger variation than the arc samples from other locations. Except one sample from Central-Eastern Aleutian arc with obviously heavy δ137/134Ba values (0.27‰), all other samples from Kamchatka, Central-Eastern Aleutian, Southern Lesser Antilles arcs are within the range of OIB. The δ137/134Ba is not correlated with the distance to trench, partial melting degrees (Mg#), or subducting slab-derived components. The samples enriched with heavy Ba isotopes have low Ba contents, indicating that Ba isotopes can be fractionated at the beginning of dehydration process with small amount of Ba releasing to the mantle wedge. With the dehydration degree increasing, more Ba of the subducted slab can be added to the source of arc lavas, likely homogenizing the Ba isotope signatures. 1. Rudnick, R., 1995 Nature; 2. Tatsumi, Y. & Kogiso, T., 2003; 3. Sun, W., et al., 2015 Ore Geol. Rev.; 4. Pearce, J., & Peate, D., 1995 Annu. Rev. Earth Planet. Sci.; 5. Pilet, S., et al., 2011 J. Petrol.; 6. Sun S. & McDonough, W., 1989; 7. Rudnick, R. & Gao, S., 2003 Treatise on geochem.; 8. Plank, T. & Langmuir, C., 1998, CG; 9. Hawkesworth, C. & Norry, M., 1983 Shiva Pub.; 10. Murphy, D., et al., 2002 J. Petrol.; 11. Kuritani, T., et al., 2011 Nat. Geosci.

Reactive Transport of Slab-Derived Carbonatitic Melts in the Deep Upper Mantle and Generation of Kimberlites

NASA Astrophysics Data System (ADS)

Sun, C.; Dasgupta, R.

2017-12-01

Kimberlite is a diamond-bearing CO2-rich ultramafic magma from the mantle at depths of >200 km, featured by enrichment of incompatible elements [1]. It has been considered significant for understanding mantle geochemistry and particularly for providing information of deep carbon cycle. Recent experimental studies suggested that partial melts of carbonated peridotites at high pressures and temperatures could resemble the MgO (>20 wt%) and enriched incompatible elements in kimberlites only when the source experienced refertilization with perhaps prior depletion (e.g., [2]). Although addition of CO2 and incompatible elements in the deep mantle is often linked to subducted components, partial melts directly from carbonated oceanic crusts do not have high enough MgO (e.g., ≤8.2 wt%; [3]). A crucial question is how slab-derived CO2-rich melt evolves in reaction with ambient mantle, which may provide a feasible mechanism for kimberlite generation. To investigate the fate of slab-derived carbonatitic melt in the deep ambient mantle, we have performed multi-anvil experiments at 7-10 GPa and 1400-1450 °C. The starting compositions were synthesized by mixing a fertile peridotite composition, KLB-1, with variable proportions (0-45 wt.%) of Ca-rich carbonatitic melt similar to those derived from a carbonated ocean crust at 13-21 GPa [3]. Experiments were performed in Pt, Pt/Gr, Au-Pd and Au-Pd/Gr capsules, and the experimental phases include olivine ± opx + cpx + majoritic garnet ± carbonated silicate melt. With the increase of melt-rock ratios, experimental melts become progressively enriched in CaO (13.0-23.1 wt%) and CO2 (14.2-38.7 wt%) but depleted in MgO (28.9-19.9 wt%), SiO2 (33.1-7.9 wt%), and Al2O3 (2.7-0.2 wt%). The net flux of melt increases with the increase of infiltrating carbonatitic melt proportion and with the decrease of pressure. Kimberlite melts were produced from experiments with 5-25 wt% infiltrating carbonatitic melts by dissolution of olivine and orthopyroxene and precipitation of clinopyroxene. Thus, a localized influx of slab-derived CO2-rich melts can enlarge the mantle porosity, enhance melt focusing, and initiate a channelized flow of kimberlite melts. [1] Becker & Le Roex (2006) J. Pet. 47: 673-703; [2] Brey et al. (2008) J. Pet. 49: 797-821; [3] Thomson et al. (2016) Nature 529: 76-79.

Deep mantle: Enriched carbon source detected

NASA Astrophysics Data System (ADS)

Barry, Peter H.

2017-09-01

Estimates of carbon in the deep mantle vary by more than an order of magnitude. Coupled volcanic CO2 emission data and magma supply rates reveal a carbon-rich mantle plume source region beneath Hawai'i with 40% more carbon than previous estimates.

Lead Isotope Compositions of Acid Residues from Olivine-Phyric Shergottite Tissint: Implications for Heterogeneous Shergottite Source Reservoirs

NASA Technical Reports Server (NTRS)

Moriwaki, R.; Usui, T.; Yokoyama, T.; Simon, J. I.; Jones, J. H.

2015-01-01

Geochemical studies of shergottites suggest that their parental magmas reflect mixtures between at least two distinct geochemical source reservoirs, producing correlations between radiogenic isotope compositions and trace element abundances. These correlations have been interpreted as indicating the presence of a reduced, incompatible element- depleted reservoir and an oxidized, incompatible- element-enriched reservoir. The former is clearly a depleted mantle source, but there is ongoing debate regarding the origin of the enriched reservoir. Two contrasting models have been proposed regarding the location and mixing process of the two geochemical source reservoirs: (1) assimilation of oxidized crust by mantle derived, reduced magmas, or (2) mixing of two distinct mantle reservoirs during melting. The former requires the ancient Martian crust to be the enriched source (crustal assimilation), whereas the latter requires isolation of a long-lived enriched mantle domain that probably originated from residual melts formed during solidification of a magma ocean (heterogeneous mantle model). This study conducts Pb isotope and trace element concentration analyses of sequential acid-leaching fractions (leachates and the final residues) from the geochemically depleted olivine-phyric shergottite Tissint. The results suggest that the Tissint magma is not isotopically uniform and sampled at least two geochemical source reservoirs, implying that either crustal assimilation or magma mixing would have played a role in the Tissint petrogenesis.

Paleoproterozoic mantle enrichment beneath the Fennoscandian Shield: Isotopic insight from carbonatites and lamprophyres

NASA Astrophysics Data System (ADS)

Woodard, Jeremy; Huhma, Hannu

2015-11-01

The isotope geochemistry of carbonatite from Naantali, southwest Finland as well as lamprophyres from North Savo, eastern Finland and the NW Ladoga region, northwest Russia has been investigated. These Paleoproterozoic dykes represent melting of an enriched mantle source spread over a 96,000 km2 area within the Fennoscandian Shield and intruded during post-collisional extension. The carbonatites have εNd(T) ranging from -0.8 to + 0.4, while lamprophyres have εNd(T) between -0.8 and + 0.3. 87Sr/86Sr ratios from the primary carbonatite samples from Naantali form a tight cluster between 0.70283 and 0.70303. For the lamprophyres, 87Sr/86Sr ratios range from 0.70327-0.70339 from NW Ladoga and 0.70316-0.70327 from North Savo. These characteristics are consistent with derivation from an enriched mantle showing an EMII trend, formed when sediments of mixed Archean and Proterozoic provenance were recycled back into the mantle via subduction during the preceding Svecofennian orogeny. Linear mixing of these subducted sediments and depleted mantle shows that a multistage process of enrichment is required to produce the observed isotope compositions. Batch melting of the subducted sediment first generated hydrous alkaline silicate melt, which crystallised as mica- and amphibole-rich veins in the mantle wedge. Continued melting of the subducted material under higher P-T conditions produced carbonatite melt, which infiltrated preferentially into this vein network. Assuming the silicate melt exerts greater influence on 87Sr/86Sr ratios while the carbonatite more greatly affects 143Nd/144Nd ratios, the model predicts significant regional variation in the silicate metasomatism with more consistent carbonatite metasomatism throughout the Fennoscandian subcontinental lithospheric mantle. The subducted sediments were likely also rich in organic matter, resulting in highly negative δ13C in mantle carbonates. The model predicts a higher content of organic carbon in the sediments in close proximity to the Archean continent, decreasing with distance.

Lithospheric thickness controlled compositional variations in potassic basalts of Northeast China by melt-rock interactions

NASA Astrophysics Data System (ADS)

Liu, Jian-Qiang; Chen, Li-Hui; Zeng, Gang; Wang, Xiao-Jun; Zhong, Yuan; Yu, Xun

2016-03-01

Melt-rock interaction is a common mantle process; however, it remains unclear how this process affects the composition of potassic basalt. Here we present a case study to highlight the link between compositional variations in the potassic basalts and melt-rock interaction in cold lithosphere. Cenozoic potassic basalts in Northeast China are strongly enriched in incompatible elements and show EM1-type Sr-Nd-Pb isotopes, suggesting an enriched mantle source. These rocks show good correlations between 87Sr/86Sr and K2O/Na2O and Rb/Nb. Notably, these ratios decrease with increasing lithospheric thickness, which may reflect melt-lithosphere interaction. Phlogopite precipitated when potassic melts passed through the lithospheric mantle, and K and Rb contents of the residual melts decreased over time. The thicker the lithosphere, the greater the loss of K and Rb from the magma. Therefore, the compositions of potassic basalts were controlled by both their enriched sources and reactions with lithospheric mantle.

Constraints on the coupled thermal evolution of the Earth's core and mantle, the age of the inner core, and the origin of the 186Os/188Os “core signal” in plume-derived lavas

NASA Astrophysics Data System (ADS)

Lassiter, J. C.

2006-10-01

The possibility that some mantle plumes may carry a geochemical signature of core/mantle interaction has rightly generated considerable interest and attention in recent years. Correlated 186Os- 187Os enrichments in some plume-derived lavas (Hawaii, Gorgona, Kostomuksha) have been interpreted as deriving from an outer core with elevated Pt/Os and Re/Os ratios due to the solidification of the Earth's inner core (c.f., [A.D. Brandon, R.J. Walker, The debate over core-mantle interaction, Earth Planet. Sci. Lett. 232 (2005) 211-225.] and references therein). Conclusive identification of a "core signal" in plume-derived lavas would profoundly influence our understanding of mantle convection and evolution. This paper reevaluates the Os-isotope evidence for core/mantle interaction by examining other geochemical constraints on core/mantle interaction, geophysical constraints on the thermal evolution of the outer core, and geochemical and cosmochemical constraints on the abundance of heat-producing elements in the core. Additional study of metal/silicate and sulfide/silicate partitioning of K, Pb, and other trace elements is needed to more tightly constrain the likely starting composition of the Earth's core. However, available data suggest that the observed 186Os enrichments in Hawaiian and other plume-derived lavas are unlikely to derive from core/mantle interaction. 1) Core/mantle interaction sufficient to produce the observed 186Os enrichments would likely have significant effects on other tracers such as Pb- and W-isotopes that are not observed. 2) Significant partitioning of K or other heat-producing elements into the core would produce a "core depletion" pattern in the Silicate Earth very different from that observed. 3) In the absence of heat-producing elements in the core, core/mantle heat flow of ˜ 6-15 TW estimated from several independent geophysical constraints suggests an inner core age (< ˜ 2.5 Ga) too young for the outer core to have developed a significant 186Os enrichment. Core/mantle thermal and chemical interaction remains an important problem that warrants future research. However, Os-isotopes may have only limited utility in this area due to the relatively young age of the Earth's inner core.

Origin and evolution of rare amphibole-bearing mantle peridotites from Wilcza Góra (SW Poland), Central Europe

NASA Astrophysics Data System (ADS)

Matusiak-Małek, Magdalena; Puziewicz, Jacek; Ntaflos, Theodoros; Grégoire, Michel; Kukuła, Anna; Wojtulek, Piotr Marian

2017-08-01

Mantle xenoliths in the 20 Ma Wilcza Góra basanite (Lower Silesia, NE Bohemian Massif) are mostly harzburgites, some with amphibole which is exceptional in the region. Forsterite content in olivine defines two Groups of peridotites: Group A (Fo89.1-91.5) and Group B (Fo84.2-89.2). Hornblende-clinopyroxenite, websterite and one composite xenolith consisting of dunite, olivine-hornblendite and pyroxene-hornblende-peridotite contain olivine with Fo77.3-82.5 and are classified as Group C. Group A xenoliths contain Al-poor orthopyroxene and some contain LREE-enriched clinopyroxene with negative Ti, Zr-Hf and Nb-Ta anomalies. Spinel (Cr# 0.57-0.68) is scarce in Group A, and Cr-rich pargasite occurs in only two xenoliths. Group B xenoliths contain less magnesian orthopyroxene and clinopyroxene. The REE patterns of Group B clinopyroxene are convex downward, less enriched in LREE and have smaller negative Ti, Zr-Hf and Nb-Ta anomalies than those in Group A. The Cr# in Group B spinel is 0.26-0.56, while pargasite is Ti-rich and Cr-poor. Clinopyroxene from Group C is low magnesian, slightly enriched in LREE and has no negative Ti, Zr-Hf and Nb-Ta anomalies. Group C pargasite is rich in Ti and poor in Cr. Equilibration temperatures recorded in all groups vary within the range of 905-970 °C. Xenoliths from Wilcza Góra record a polyphase lithospheric mantle evolution, starting with melting which extracted ca. 30% melt from the protolith and left a harzburgite residuum depleted in Al, lacking clinopyroxene and containing rare Cr-rich spinel. This residuum was later overprinted by chromatographic metasomatism by carbonated hydrous silicate melt related to Cenozoic volcanism. The metasomatic agent was locally hydrous enough to enable amphibole to crystallize. The Group C pyroxenites formed directly from the metasomatic melt or during peridotite-melt reactions at high melt-rock ratio. The melt is inferred to have percolated through the wall-rock peridotite, decreasing its amount and changing composition (and that of the crystallizing clinopyroxene and amphibole) as it differentiated chromatographically from Groups B to A. Enrichment in carbonatite component occurred in the further parts of a chromatographic column. Group B peridotites closest to the source of the metasomatic agent were percolated by an iron-rich melt. The latter, aside from crystallizing clinopyroxene and amphibole, caused Fe-enrichment in the host harzburgite. Such a metasomatic history is typical for the lithospheric mantle located beneath the northern margin of the Bohemian Massif, but Wilcza Góra is the only locality, where activity of a hydrous metasomatic agent is recorded. Thus, the lithospheric mantle in this area was affected by mafic silicate metasomatic agents of variable compositions.

Oceanic magmatic evolution during ocean opening under influence of mantle plume

NASA Astrophysics Data System (ADS)

Sushchevskaya, Nadezhda; Melanholina, Elena; Belyatsky, Boris; Krymsky, Robert; Migdisova, Natalya

2015-04-01

Petrology, geochemistry and geophysics as well as numerical simulation of spreading processes in plume impact environments on examples of Atlantic Ocean Iceland and the Central Atlantic plumes and Kerguelen plume in the Indian Ocean reveal: - under interaction of large plume and continental landmass the plume can contribute to splitting off individual lithosphere blocks, and their subsequent movement into the emergent ocean. At the same time enriched plume components often have geochemical characteristics of the intact continental lithosphere by early plume exposure. This is typical for trap magmatism in Antarctica, and for magmatism of North and Central Atlantic margins; - in the course of the geodynamic reconstruction under the whole region of the South Atlantic was formed (not in one step) metasomatized enriched sub-oceanic mantle with pyroxenite mantle geochemical characteristics and isotopic composition of enriched HIMU and EM-2 sources. That is typical for most of the islands in the West Antarctic. This mantle through spreading axes jumping involved in different proportions in the melting under the influence of higher-temperature rising asthenospheric lherzolite mantle; - CAP activity was brief enough (200 ± 2 Ma), but Karoo-Maud plume worked for a longer time and continued from 180 to 170 Ma ago in the main phase. Plume impact within Antarctica distributed to the South and to the East, leading to the formation of extended igneous provinces along the Transantarctic Mountains and along the east coast (Queen Maud Land province and Schirmacher Oasis). Moreover, this plume activity may be continued later on, after about 40 million years cessation, as Kerguelen plume within the newly-formed Indian Ocean, significantly affects the nature of the rift magmatism; - a large extended uplift in the eastern part of the Indian Ocean - Southeastern Indian Ridge (SEIR) was formed on the ancient spreading Wharton ridge near active Kerguelen plume. The strongest plume influence on the SEIR formation occurred 70-50 mln years ago, when the process of primary magma generation happened at high degrees of melting (up to 30%), which is not typical for spreading ridges of the Atlantic and Pacific Oceans. According to geochemical characteristics of the Kerguelen Plateau and SEIR magma sources close to each other, and have an enriched source of more typical for Kerguelen plume magmas and diluted by depleted substance for SEIR melts. Appearance of magmatism on the Antarctic margin about 56 thousand years ago, in the form of a stratovolcano Gaussberg indicates sublithospheric Kerguelen plume distribution in the south-west direction. The source of primary magmas (lamproite composition) is an ancient Gondwana lithosphere, has undergone repeated changes in the early stages of evolution during which it was significantly enriched in volatile and lithophile elements, and radiogenic Sr and Pb.

Chemical layering in the upper mantle of Mars: Evidence from olivine-hosted melt inclusions in Tissint

NASA Astrophysics Data System (ADS)

Basu Sarbadhikari, A.; Babu, E. V. S. S. K.; Vijaya Kumar, T.

2017-02-01

Melting of Martian mantle, formation, and evolution of primary magma from the depleted mantle were previously modeled from experimental petrology and geochemical studies of Martian meteorites. Based on in situ major and trace element study of a range of olivine-hosted melt inclusions in various stages of crystallization of Tissint, a depleted olivine-phyric shergottite, we further constrain different stages of depletion and enrichment in the depleted mantle source of the shergottite suite. Two types of melt inclusions were petrographically recognized. Type I melt inclusions occur in the megacrystic olivine core (Fo76-70), while type II melt inclusions are hosted by the outer mantle of the olivine (Fo66-55). REE-plot indicates type I melt inclusions, which are unique because they represent the most depleted trace element data from the parent magmas of all the depleted shergottites, are an order of magnitude depleted compared to the type II melt inclusions. The absolute REE content of type II displays parallel trend but somewhat lower value than the Tissint whole-rock. Model calculations indicate two-stage mantle melting events followed by enrichment through mixing with a hypothetical residual melt from solidifying magma ocean. This resulted in 10 times enrichment of incompatible trace elements from parent magma stage to the remaining melt after 45% crystallization, simulating the whole-rock of Tissint. We rule out any assimilation due to crustal recycling into the upper mantle, as proposed by a recent study. Rather, we propose the presence of Al, Ca, Na, P, and REE-rich layer at the shallower upper mantle above the depleted mantle source region during the geologic evolution of Mars.

Back-arc basalts from the Loncopue graben (Province of Neuquen, Argentina)

NASA Astrophysics Data System (ADS)

Varekamp, J. C.; Hesse, A.; Mandeville, C. W.

2010-11-01

Young basaltic back-arc volcanoes occur east of the main Andes chain at about 37.5°-39°S in the Loncopue graben, Province of Neuquen, Argentina. These olivine-rich basalts and trachybasalts have up to 8% MgO, with high Ni and Cr contents, but highly variable incompatible element concentrations. Mafic lava flows and cinder cones at the southern end of the graben lack phenocrystic plagioclase. The northern samples have relative Ta-Nb depletions and K, Pb and LREE enrichment. These samples strongly resemble rocks of the nearby arc volcanoes Copahue and Caviahue, including their Fe-Ti enrichment relative to the main Andes arc rocks. The Sr, Nd and Pb isotope ratios show that the source regions of these back-arc basalts are enriched in subducted components that were depleted in the aqueous mobile elements such as Cs, Sr and Ba as a result of prior extractions from the subducted complex below the main arc. Some mafic flows show slightly low 206Pb/ 204Pb and 143Nd/ 144Nd values as well as incompatible trace element ratios similar to southern Patagonia plateau back-arc basalts, suggesting contributions from an EM1 mantle source. Geothermometry and barometry suggest that the basalts crystallized and fractionated small amounts of olivine and spinel at ˜ 35 km depth at temperatures of 1170-1220 °C, at about QFM + 0.5 to QFM + 1 with 1-2% H 2O, and then rose rapidly to the surface. The Loncopue graben back-arc basalts are transitional in composition between the South Patagonia back-arc plateau basalts and the Caviahue and Copahue arc volcanoes to the northwest. The EM1 source endmember is possibly the subcontinental lithospheric mantle. Strong variations in incompatible element enrichment and isotopic compositions between closely spaced cinder cones and lava flows suggest a heterogeneous mantle source for the Loncopue graben volcanics.

Petrological processes in mantle plume heads: Evidence from study of mantle xenoliths in the late Cenozoic alkali Fe-Ti basalts in Western Syria

NASA Astrophysics Data System (ADS)

Sharkov, Evgenii

2015-04-01

It is consensus now that within-plate magmatism is considered with ascending of mantle plumes and adiabatic melting of their head. At the same time composition of the plumes' matter and conditions of its adiabatic melting are unclear yet. The major source of objective information about it can be mantle xenoliths in alkali basalts and basanites which represent fragments of material of the plume heads above magma-generation zone. They are not represent material in melting zone, however, carry important information about material of modern mantle plumes, its phase composition and components, involved in melting. Populations of mantle xenoliths in basalts are characterized by surprising sameness in the world and represented by two major types: (1) dominated rocks of ``green'' series, and (2) more rare rocks of ``black'' series, which formed veins in the ``green'' series matrix. It can evidence about common composition of plume material in global scale. In other words, the both series of xenoliths represent two types of material of thermochemical mantle plumes, ascended from core-mantle boundary (Maruyama, 1994; Dobretsov et al., 2001). The same types of xenoliths are found in basalts and basanites of Western Syria (Sharkov et al., 1996). Rocks of ``green'' series are represented by Sp peridotites with cataclastic and protogranular structures and vary in composition from dominated spinel lherzolites to spinel harzburgites and rare spinel pyroxenites (websterites). It is probably evidence about incomplete homogenizing of the plume head matter, where material, underwent by partial melting, adjoins with more fertile material. Such heterogeneity was survived due to quick cooling of upper rim of the plume head in contact with relatively cold lithosphere. Essential role among xenoliths of the ``black'' series play Al-Ti-augite and water-bearing phases like hornblende (kaersutute) and Ti-phlogopite. Rocks of this series are represented by wehrlite, clinopyroxenite, amphibole clinopyroxenite, hornbledite, etc. as well as megacrysts of Al-Ti-augite, kaersutite, ilmenite, sanidine, etc. Numerous vesicles often occurred in megacrysts, especially in kaersurtite. Sp peridotites of the matrix are sharply different on their geochemical features from the ``black series'' rocks (in this case, megacrysts of kaersutite) which are the most close to composition of xenoliths-bearing alkali basalts. From this follows that geochemistry of plume-related basalts was determined by mantle fluids which occurred in magma-generation zone. Very likely, that these fluids, enriched in Fe, Ti, LREE, alkalis, and incompatible elements, initially were parts of intergranular material of original mantle plume material and were released due to its decompression. Because their high mobility, the fluids percolated upwards and accumulated in the upper part of the mantle plume head, where promoted its melting by lowering of solidus of the matter. Excess of the fluids gathered beneath the cooled upper rim and penetrated in its rocks which led to appearance of centers of secondary melting (melt-pockets). Very likely, that these secondary melts formed rocks of the ``black series'' (Ismail et al., 2008;Ryabchkov et al., 2011; Ma et al., 2014). According to geobarometric estimations, Sp peridotite xenoliths from Syria derived from depths 24-42 km (0.8-1.4 GPa) under temperatures 896-980oC; formation of melt-pockets, enriched in volatiles, occurred at the depths 21-27 km (0.7-0.9 GPa) under 826-981oC (Sharkov et al., 1996; Ismail et al., 2008; Ma et al., 2014). From this follows that plumeheads reached depths approximately 21-30 km which is in agree with practically absence of lower-crustal xenoliths in the populations. One of the problems of plume-related magmatism is coexisting of alkali and tholeiitic basalts, which origin often considered with different PT conditions. However, these basalt not rarely interlayered, especially at low and middle levels of LIPs or in single volcanoes (Hawaii, Etna, etc.) which is not in a good agreement with such idea. We suggest that the situation can be more likely explained by nonuniform impregnation of peridotite matrix with fluid components which composition and/or quantity can play essential role in composition of smeltings. It is especially important because even small differences in their ñomposition near to plane of SiO2 saturation in ``basalt tetrahedron'' (Yoder and Tilley, 1962) lead to appearance of Ne-normative or Ne-free melts at practically similar PT conditions. Thus, judging on composition of the mantle xenoliths in basalts of all occurrences in the world, quite possible that Sp peridotites (mainly lherzolites) together with intergranular geochemical-enriched fluid components represent the matter of the modern thermochemical mantle plumes. Origin of two major types of the plume-related magmas, probably, considered with fluid regime in the plume head.

Primitive magmas at five Cascade volcanic fields: Melts from hot, heterogeneous sub-arc mantle

USGS Publications Warehouse

Bacon, C.R.; Bruggman, P.E.; Christiansen, R.L.; Clynne, M.A.; Donnelly-Nolan, J. M.; Hildreth, W.

1997-01-01

Major and trace element concentrations, including REE by isotope dilution, and Sr, Nd, Pb, and O isotope ratios have been determined for 38 mafic lavas from the Mount Adams, Crater Lake, Mount Shasta, Medicine Lake, and Lassen volcanic fields, in the Cascade arc, northwestern part of the United States. Many of the samples have a high Mg# [100Mg/(Mg + FeT) > 60] and Ni content (>140 ppm) such that we consider them to be primitive. We recognize three end-member primitive magma groups in the Cascades, characterized mainly by their trace-element and alkali-metal abundances: (1) High-alumina olivine tholeiite (HAOT) has trace element abundances similar to N-MORB, except for slightly elevated LILE, and has Eu/Eu* > 1. (2) Arc basalt and basaltic andesite have notably higher LILE contents, generally have higher SiO2 contents, are more oxidized, and have higher Cr for a given Ni abundance than HAOT. These lavas show relative depletion in HFSE, have lower HREE and higher LREE than HAOT, and have smaller Eu/Eu* (0.94-1.06). (3) Alkali basalt from the Simcoe volcanic field east of Mount Adams represents the third end-member, which contributes an intraplate geochemical signature to magma compositions. Notable geochemical features among the volcanic fields are: (1) Mount Adams rocks are richest in Fe and most incompatible elements including HFSE; (2) the most incompatible-element depleted lavas occur at Medicine Lake; (3) all centers have relatively primitive lavas with high LILE/HFSE ratios but only the Mount Adams, Lassen, and Medicine Lake volcanic fields also have relatively primitive rocks with an intraplate geochemical signature; (4) there is a tendency for increasing 87Sr/86Sr, 207Pb/204Pb, and ??18O and decreasing 206Pb/204Pb and 143Nd/144Nd from north to south. The three end-member Cascade magma types reflect contributions from three mantle components: depleted sub-arc mantle modestly enriched in LILE during ancient subduction; a modern, hydrous subduction component; and OIB-source-like domains. Lavas with arc and intraplate (OIB) geochemical signatures were erupted close to HAOT, and many lavas are blends of two or more magma types. Pre-eruptive H2O contents of HAOT, coupled with phase-equilibrium studies, suggest that these magmas were relatively dry and last equilibrated in the mantle wedge at temperatures of ???1300??C and depths of ???40 km, virtually at the base of the crust. Arc basalt and basaltic andesite represent greater extents of melting than HAOT, presumably in the same general thermal regime but at somewhat lower mantle separation temperatures, of domains of sub-arc mantle that have been enriched by a hydrous subduction component derived from the young, relatively hot Juan de Fuca plate. The primitive magmas originated by partial melting in response to adiabatic upwelling within the mantle wedge. Tectonic extension in this part of the Cascade arc, one characterized by slow oblique convergence, contributes to mantle upwelling and facilitates eruption of primitive magmas.

Geochemical characteristics of the La Réunion mantle plume source inferred from olivine-hosted melt inclusions from the adventive cones of Piton de la Fournaise volcano (La Réunion Island)

NASA Astrophysics Data System (ADS)

Valer, Marina; Schiano, Pierre; Bachèlery, Patrick

2017-09-01

Major and trace element compositions were obtained for bulk rocks and melt inclusions hosted in olivine crystals (Fo > 85) from the adventive cones of the Piton de La Fournaise volcano (La Réunion Island). Ratios of highly incompatible trace elements for these magmas are used to identify the nature of the La Réunion mantle plume source. Although adventive cone lavas display unusual major element compositions compared to the historical lavas of the volcano (e.g., lower CaO/Al2O3), trace element data suggest that the magmas emitted by the adventive cones originate from a common chemical source. This source may correspond to either a homogeneous mixed source of different mantle components or a near-primitive less-differentiated mantle source. The melt inclusions display ratios of highly incompatible elements (e.g., Th/La, Nb/La) which are similar to primitive mantle values, and lower Nb/U ratios compared to most oceanic basalts. These results and previous isotopic and trace element data suggest that La Réunion plume samples a source which is intermediate between a primitive-like mantle domain and a slightly depleted one almost unaffected by the recycling processes. This source could have originated from early depletion of the primitive mantle. Assuming a depletion 4.45 Gyr ago, 10% melting of this slightly depleted source could explain the enriched trace element concentrations of the melt inclusions.

Memory-enriched CAR-T Cells Immunotherapy for B Cell Lymphoma

ClinicalTrials.gov

2016-04-25

Recurrent Adult Diffuse Large Cell Lymphoma; Recurrent Follicular Lymphoma; Recurrent Mantle Cell Lymphoma; Stage III Adult Diffuse Large Cell Lymphoma; Stage III Follicular Lymphoma; Stage III Mantle Cell Lymphoma; Stage IV Adult Diffuse Large Cell Lymphoma; Stage IV Follicular Lymphoma; Stage IV Mantle Cell Lymphoma

The Oxidation State of Fe in Glasses from the Galapagos Archipelago: Variable Oxygen Fugacity as a Function of Mantle Source

NASA Astrophysics Data System (ADS)

Peterson, M. E.; Kelley, K. A.; Cottrell, E.; Saal, A. E.; Kurz, M. D.

2015-12-01

The oxidation state of the mantle plays an intrinsic role in the magmatic evolution of the Earth. Here we present new μ-XANES measurements of Fe3+/ΣFe ratios (a proxy for ƒO2) in a suite of submarine glasses from the Galapagos Archipelago. Using previously presented major, trace, and volatile elements and isotopic data for 4 groups of glass that come from distinct mantle sources (depleted upper mantle, 2 recycled, and a primitive mantle source) we show that Fe3+/ΣFe ratios vary both with the influence of shallow level processes and with variations in mantle source. Fe3+/ΣFe ratios increase with differentiation (i.e. decreasing MgO), but show a large variation at a given MgO. Progressive degassing of sulfur accompanies decreasing Fe3+/ΣFe ratios, while assimilation of hydrothermally altered crust (as indicated by increasing Sr/Sr*) is shown to increase Fe3+/ΣFe ratios. After taking these processes into account, there is still variability in the Fe3+/ΣFe ratios of the isotopically distinct sample suites studied, yielding a magmatic ƒO2 that ranges from ΔQFM = +0.16 to +0.74 (error < 0.5 log units) and showing that oxidation state varies as a function of mantle source composition in the Galapagos hotspot system. After correcting back to a common MgO content = 8.0 wt%, the trace element depleted group similar to MORB (ITD), and the group similar to Pinta (WD = high Th/La, Δ7/4, Δ8/4 ratios) show Fe3+/ΣFe ratios within the range of MORB (average ITD = 0.162 ± 0.003 and WD = 0.164 ± 0.006). Another trace element enriched group similar to Sierra Negra and Cerro Azul (ITE = enriched Sr and Pb isotopes) shows evidence of mixing between oxidized and reduced sources (ITE oxidized end-member = 0.177). This suggests that mantle sources in the Galapagos that are thought to contain recycled components (i.e., WD and ITE groups) have distinct oxidation states. The high 3He/4He Fernandina samples (HHe group) are shown to be the most oxidized (ave. 0.175 ± 0.006). With C/3He ratios an order of magnitude greater than MORB this suggests that the primitive mantle is a more carbonated and oxidized source than the depleted upper mantle.

Formation and Preservation of the Depleted and Enriched Shergottite Isotopic Reservoirs in a Convecting Martian Mantle

NASA Technical Reports Server (NTRS)

Kiefer, Walter S.; Jones, John H.

2015-01-01

There is compelling isotopic and crater density evidence for geologically recent volcanism on Mars, in the last 100-200 million years and possibly in the last 50 million years. This volcanism is due to adiabatic decompression melting and thus requires some type of present-day convective upwelling in the martian mantle. On the other hand, martian meteorites preserve evidence for at least 3 distinct radiogenic isotopic reservoirs. Anomalies in short-lived isotopic systems (Sm-146, Nd-142, Hf-182, W-182) require that these reservoirs must have developed in the first 50 to 100 million years of Solar System history. The long-term preservation of chemically distinct reservoirs has sometimes been interpreted as evidence for the absence of mantle convection and convective mixing on Mars for most of martian history, a conclusion which is at odds with the evidence for young volcanism. This apparent paradox can be resolved by recognizing that a variety of processes, including both inefficient mantle mixing and geographic separation of isotopic reservoirs, may preserve isotopic heterogeneity on Mars in an actively convecting mantle. Here, we focus on the formation and preservation of the depleted and enriched isotopic and trace element reservoirs in the shergottites. In particular, we explore the possible roles of processes such as chemical diffusion and metasomatism in dikes and magma chambers for creating the isotopically enriched shergottites. We also consider processes that may preserve the enriched reservoir against convective mixing for most of martian history.

Chlorine and fluorine partition coefficients and abundances in sub-arc mantle xenoliths (Kamchatka, Russia): Implications for melt generation and volatile recycling processes in subduction zones

NASA Astrophysics Data System (ADS)

Bénard, A.; Koga, K. T.; Shimizu, N.; Kendrick, M. A.; Ionov, D. A.; Nebel, O.; Arculus, R. J.

2017-02-01

We report chlorine (Cl) and fluorine (F) abundances in minerals, interstitial glasses, and melt inclusions in 12 andesite-hosted, spinel harzburgite xenoliths and crosscutting pyroxenite veins exhumed from the sub-arc lithospheric mantle beneath Avacha volcano in the Kamchatka Arc (NE Russia). The data are used to calculate equilibrium mineral-melt partition coefficients (D mineral / melt) for Cl and F relevant to subduction-zone processes and unravel the history of volatile depletion and enrichment mechanisms in an arc setting. Chlorine is ∼100 times more incompatible in pyroxenes (DClmineral/melt = 0.005-0.008 [±0.002-0.003]) than F (DFmineral/melt = 0.50-0.57 [±0.21-0.24]), which indicates that partial melting of mantle sources leads to strong depletions in Cl relative to F in the residues. The data set in this study suggests a strong control of melt composition on DCl,Fpyroxene/melt, in particular H2O contents and Al/(Al + Si), which is in line with recent experiments. Fluorine is compatible in Ca-amphibole in the 'wet' sub-arc mantle (DFamphibole/melt = 3.5-3.7 [±1.5]) but not Cl (DClamphibole/melt = 0.03-0.05 [±0.01-0.03]), indicating that amphibole may fractionate F from Cl in the mantle wedge. The inter-mineral partition coefficients for Cl and F in this study are consistent amongst different harzburgite samples, whether they contain glass or not. In particular, disseminated amphibole hosts much of the Cl and F bulk rock budgets of spinel harzburgites (DClamphibole/pyroxene up to 14 and DFamphibole/pyroxene up to 40). Chlorine and fluorine are variably enriched (up to 1500 ppm Cl and 750 ppm F) in the parental arc picrite and boninite melts of primitive pyroxenite veins (and related melt inclusions) crosscutting spinel harzburgites. Based on the data in this study, the main inferences on the behaviour of Cl and F during melting and metasomatic processes in the sub-arc mantle are as follow: (i) Melting models show that most depleted mantle protoliths of intra-oceanic arc sources can have extremely low Cl/F (0.002-0.007) before being overprinted by subduction-derived components. (ii) Chlorine has a higher percolation distance in the mantle than F. Even for small fluid or melt volumes, Cl and F signatures of partial melting are overprinted by those of pervasive percolation, which increases Cl/F in percolating agents and bulk peridotites during chromatographic interaction and/or amphibole-forming metasomatic reactions. These processes ultimately control the bulk Cl and F compositions of the residual mantle lithosphere beneath arcs, and likely in other tectonic settings. (iii) Fluxed melting models suggest that Cl enrichment in arc picrite and boninite melts in this study, and in many arc melt inclusions reported in the literature, could be related to the infiltration of high Cl/F fluids derived from subducted serpentinite or altered crust in mantle wedge sources. However, these high Cl/F signatures should be re-evaluated with new models in light of the possible overprint of pervasive percolation effects in the mantle. The breakdown of amphibole (and/or mica) in the deep metasomatised mantle at higher pressure and temperature conditions than in the slab may explain, at least in part, the positive correlations between F abundances and Cl/F in primitive arc melt inclusions and slab depth.

Understanding the geodynamic setting of São Miguel, Azores: A peculiar bit of mantle in the Central Atlantic

NASA Astrophysics Data System (ADS)

Wilson, M.; Houlie, N.; Khan, A.; Lithgow-Bertelloni, C. R.

2012-12-01

The Azores Plateau and Archipelago in the Central Atlantic Ocean has traditionally been considered as the surface expression of a deep mantle plume or hotspot that has interacted with a mid-ocean ridge. It is geodynamically associated with the triple junction between the North American, African and Eurasian plates. (Yang et al., 2006) used finite frequency seismic tomography to demonstrate the presence of a zone of low P-wave velocities (peak magnitude -1.5%) in the uppermost 200km of the mantle beneath the plateau. The tomographic model is consistent with SW deflection of a mantle plume by regional upper mantle shear flow driven by absolute plate motions. The volcanic island of Sao Miguel is located within the Terceira Rift, believed to represent the boundary between the African and Eurasian plates; magmatic activity has been characterised by abundant basaltic eruptions in the past 30,000 years. The basalts are distinctive within the spectrum of global ocean island basalts for their wide range in isotopic composition, particularly in 87Sr/86Sr. Their Sr-Nd-Pb isotopic compositions show systematic variations from west to east across the island which can be interpreted in terms of melting of a two-component mantle source. The low melting point (enriched) component in the source has been attributed to recycled ancient (~3 Ga) oceanic crust(Elliott et al., 2007). Using the thermo-barometry approach of (Lee et al., 2009) we demonstrate that the pressure and temperature of magma generation below Sao Miguel increase from west (2 GPa, 1425 °C) to east (3.8 GPa, 1575 °C), consistent with partial melting along a mantle geotherm with a potential temperature of ~ 1500 °C. This is consistent with the magnitude of the thermal anomaly beneath the Azores Plateau (ΔT ~ 150-200 °C) inferred on the basis of the seismic tomography study. The site of primary magma generation extends from the base of the local lithosphere (~ 50 km) to ~ 125 km depth. To understand the geodynamic setting of the Sao Miguel magmatism we combine GPS data and mantle convection models with our interpretation of the geochemistry of the basalts. We demonstrate strong south-westerly and downward flow in the asthenospheric mantle above the Transition Zone (410 km seismic discontinuity), consistent with a zone of upper mantle shearing below the base of the lithosphere. The maximum flow velocity is broadly consistent with the depth of magma generation. The advection of the mantle with respect to the oceanic plate "moves" an isotopically distinct mantle source component beneath the active volcanoes of Sao Miguel and carries its previous melting residues to the south-west. We discuss the nature of this mantle source and its contribution to the mantle velocity anomalies determined by seismic tomography. This study opens-up new perspectives for seismic tomography and potentially new connections between the fields of geophysics and geochemistry in oceanic domains.

Constraining late stage melt-peridotite interaction in the lithospheric mantle of southern Ethiopia: evidence from lithium elemental and isotopic compositions

NASA Astrophysics Data System (ADS)

Alemayehu, Melesse; Zhang, Hong-Fu; Seitz, Hans-Michael

2017-10-01

Lithium (Li) elemental and isotopic compositions for mineral separates of coexisting olivine, orthopyroxene and clinopyroxene of mantle xenoliths from the Quaternary volcanic rocks of southern Ethiopian rift (Dillo and Megado) reveal the influence of late stage melt-peridotite interaction on the early depleted and variably metasomatized lithospheric mantle. Two types of lherzolites are reported (LREE-depleted La/Sm(N) = 0.11-0.37 × Cl and LREE-enriched, La/Sm(N) = 1.88-15.72 × Cl). The depleted lherzolites have variable range in Li concentration (olivine: 2.1-5.4 ppm; opx: 1.1-2.3 ppm; cpx: 1.0-1.8 ppm) and in Li isotopic composition (δ7Li in olivine: -9.4 to 1.5‰; in opx: -4.5 to 3.6‰; in cpx: -17.0 to 4.8‰), indicating strong disequilibrium in Li partitioning and Li isotope fractionation between samples. The enriched lherzolites have limited range in both Li abundances (olivine: 2.7-3.0 ppm; opx: 1.1-3.1 ppm; cpx: 1.1-2.3 ppm) and Li isotopic compositions (δ7Li in olivine: -1.3 to +1.3‰; in opx: -2.0 to +5.0‰; in cpx: -7.5 to +4.8‰), suggest that the earlier metasomatic event which lead to LREE enrichment could also homogenize the Li contents and its isotopes. The enriched harzburgite and clinopyroxenite minerals show limited variation in Li abundances and variable Li isotopic compositions. The Li enrichments of olivine and clinopyroxene correlate neither with the incompatible trace element enrichment nor with the Sr-Nd isotopic compositions of clinopyroxene. These observations indicate that the metasomatic events which are responsible for the LREE enrichment and for the Li addition are distinct, whereby the LREE-enrichment pre-dates the influx of Li. The presence of large Li isotopic disequilibria within and between minerals of depleted and enriched peridotites suggest that the lithospheric mantle beneath the southern Ethiopian rift has experienced recent melt-peridotite interaction. Thus, the Li data set reported in this study offer new additional evidence for the existence of late stage metasomatism, which probably occurred at shallow depth briefly before and/or during entrainment and ascent of mantle xenoliths to the surface.

Osmium-187 enrichment in some plumes: Evidence for core-mantle interaction?

USGS Publications Warehouse

Walker, R.J.; Morgan, J.W.; Horan, M.F.

1995-01-01

Calculations with data for asteroidal cores indicate that Earth's outer core may have a rhenium/osmium ratio at least 20 percent greater than that of the chondritic upper mantle, potentially leading to an outer core with an osmium-187/osmium-188 ratio at least 8 percent greater than that of chondrites. Because of the much greater abundance of osmium in the outer core relative to the mantle, even a small addition of metal to a plume ascending from the D??? layer would transfer the enriched isotopic signature to the mixture. Sources of certain plume-derived systems seem to have osmium-187/osmium-188 ratios 5 to 20 percent greater than that for chondrites, consistent with the ascent of a plume from the core-mantle boundary.

Evaluating Crustal Contamination Effects On The Lithophile Trace Element Budget Of Shergottites, NWA 856 As A Test Case

NASA Technical Reports Server (NTRS)

Brandon, A. D.; Ferdous, J.; Peslier, A. H.

2017-01-01

The issue of whether crustal contamination has affected the lithophile trace element budget of shergottites has been a point of contention for decades. The evaluation has focused on the enriched shergottite compositions as an outcome of crustal contamination of mantle-derived parent magmas or, alternatively, the compositions of these stones reflect an incompatible trace element (ITE) enriched mantle source.

Water Content in the SW USA Mantle Lithosphere: FTIR Analysis of Dish Hill and Kilbourne Hole Pyroxenites

NASA Technical Reports Server (NTRS)

Gibler, Robert; Peslier, Anne H.; Schaffer, Lillian Aurora; Brandon, Alan D.

2014-01-01

Kilbourne Hole (NM, USA) and Dish Hill (CA, USA) mantle xenoliths sample continental mantle in two different tectonic settings. Kilbourne Hole (KH) is located in the Rio Grande rift. Dish Hill (DH) is located in the southern Mojave province, an area potentially affected by subduction of the Farallon plate beneath North America. FTIR analyses were obtained on well characterized pyroxenite, dunite and wehrlite xenoliths, thought to represent crystallized melts at mantle depths. PUM normalized REE patterns of the KH bulk-rocks are slightly LREE enriched and consistent with those of liquids generated by < 5% melting of a spinel peridotite source. Clinopyroxenes contain from 272 to 313 ppm weight H2O similar to the lower limit of KH peridotite clinopyroxenes (250-530 ppm H2O). This is unexpected as crystallized melts like pyroxenites should concentrate water more than residual mantle-like peridotites, given that H is incompatible. PUM normalized bulk REE of the DH pyroxenites are characterized by flat to LREE depleted REE profiles consistent with > 6% melting of a spinel peridotite source. Pyroxenite pyroxenes have no detectable water but one DH wehrlite, which bulk-rock is LREE enriched, has 4 ppm H2O in orthopyroxene and <1ppm in clinopyroxene. The DH pyroxenites may thus come from a dry mantle source, potentially unaffected by the subduction of the Farallon plate. These water-poor melts either originated from shallow oceanic lithosphere overlaying the Farallon slab or from continental mantle formed > 2 Ga. The Farallon subduction appears to have enriched in water the southwestern United States lithospheric mantle further east than DH, beneath the Colorado plateau.

Across-arc geochemical variations in the Southern Volcanic Zone, Chile (34.5-38.0°S): Constraints on mantle wedge and slab input compositions

NASA Astrophysics Data System (ADS)

Jacques, G.; Hoernle, K.; Gill, J.; Hauff, F.; Wehrmann, H.; Garbe-Schönberg, D.; van den Bogaard, P.; Bindeman, I.; Lara, L. E.

2013-12-01

Crustal assimilation (e.g. Hildreth and Moorbath, 1988) and/or subduction erosion (e.g. Stern, 1991; Kay et al., 2005) are believed to control the geochemical variations along the northern portion of the Chilean Southern Volcanic Zone. In order to evaluate these hypotheses, we present a comprehensive geochemical data set (major and trace elements and O-Sr-Nd-Hf-Pb isotopes) from Holocene primarily olivine-bearing volcanic rocks across the arc between 34.5°S and 38.0°S, including volcanic front centers from Tinguiririca to Callaqui, the rear arc centers of Infernillo Volcanic Field, Laguna del Maule and Copahue, and extending 300 km into the backarc. We also present an equivalent data set for Chile trench sediments outboard of this profile. The volcanic arc (including volcanic front and rear arc) samples primarily range from basalt to andesite/trachyandesite, whereas the backarc rocks are low-silica alkali basalts and trachybasalts. All samples show some characteristic subduction zone trace element enrichments and depletions, but the backarc samples show the least. Backarc basalts have higher Ce/Pb, Nb/U, Nb/Zr, and Ta/Hf, and lower Ba/Nb and Ba/La, consistent with less of a slab-derived component in the backarc and, consequently, lower degrees of mantle melting. The mantle-like δ18O in olivine and plagioclase phenocrysts (volcanic arc = 4.9-5.6‰ and backarc = 5.0-5.4‰) and lack of correlation between δ18O and indices of differentiation and other isotope ratios, argue against significant crustal assimilation. Volcanic arc and backarc samples almost completely overlap in Sr and Nd isotopic composition. High precision (double-spike) Pb isotope ratios are tightly correlated, precluding significant assimilation of older sialic crust but indicating mixing between a South Atlantic Mid Ocean-Ridge Basalt (MORB) source and a slab component derived from subducted sediments and altered oceanic crust. Hf-Nd isotope ratios define separate linear arrays for the volcanic arc and backarc, neither of which trend toward subducting sediment, possibly reflecting a primarily asthenospheric mantle array for the volcanic arc and involvement of enriched Proterozoic lithospheric mantle in the backarc. We propose a quantitative mixing model between a mixed-source, slab-derived melt and a heterogeneous mantle beneath the volcanic arc. The model is consistent with local geodynamic parameters, assuming water-saturated conditions within the slab.

Generation of alkaline magmas in subduction zones by melting of mélange diapirs

NASA Astrophysics Data System (ADS)

Cruz-Uribe, A. M.; Marschall, H.; Gaetani, G. A.; Le Roux, V.

2016-12-01

Alkaline lavas occur globally in subduction-related volcanic arcs. Existing explanations for the occurrence of alkaline lavas in volcanic arcs invoke at least one - and in some cases multiple - `metasomatic' events in addition to the traditional three-component mixing of altered oceanic crust (AOC), sediment melt, and depleted mantle, in order to explain the range of rock types found in a given region. These multi-stage models posit the existence of metasomatized mantle wedge peridotite containing phlogopite or amphibole-enriched veins, which partially melt when fluxed by the addition of materials from the subducted slab. The mélange diapir model is informed by observations and modeling of the subduction side of the arc system, and predicts the generation of alkaline arc magmas by advection of buoyant material from the slab-wedge interface into the mantle wedge below arcs. Here we report results from experiments in which natural mélange materials partially melted at upper mantle conditions were found to produce alkaline magmas compositionally similar to those found in arcs worldwide. The starting material for our experiments is a chlorite-omphacite fels (SY400) from the island of Syros, Greece, that is representative of a hybrid rock containing AOC, sediment, and mantle components. Melting experiments were performed using a piston cylinder apparatus at conditions relevant to the heating-decompression path of mélange diapirs (1000-1300 °C, 1.5-2.5 GPa). The compositions of experimentally produced melts range from 51-61 wt% SiO2, and fall within the trachyte and tephrite-phonolite series (7.5-12.9 wt% Na2O+K2O). Restitic phases in equilibrium with melt include clinopyroxene, garnet (at high P), phlogopite (at high P), amphibole, olivine, rutile, and ilmenite. Partial melts produced in our experiments have trace-element abundance patterns that are typical of alkaline arc lavas, such as enrichment in large ion lithophile elements (Cs, Rb, Ba, Pb, Sr) and alkalis (K and Na), and depletion in Nb and Ta. The presence of a light rare earth element (LREE)-bearing accessory phase results in trace element fractionation by a factor of 4.2 for Nd/Hf and 2.6 for Sr/Nd. Melting of mélange diapirs provides a simple, single-stage model for the origin of alkaline magmatism in the arc and backarc regions of subduction zones.

Constraining LLSVP Buoyancy With Tidal Tomography

NASA Astrophysics Data System (ADS)

Lau, H. C. P.; Mitrovica, J. X.; Davis, J. L.; Tromp, J.; Yang, H. Y.; Al-Attar, D.

2017-12-01

Using a global GPS data set of high precision measurements of the Earth's body tide, we perform a tomographic inversion to constrain the integrated buoyancy of the Large Low Shear Velocity Provinces (LLSVPs) at the base of the mantle. As a consequence of the long-wavelength and low frequency nature of the Earth's body tide, these observations are particularly sensitivity to LLSVP buoyancy, a property of Earth's mantle that remains a source of ongoing debate. Using a probabilistic approach we find that the data are best fit when the bottom two thirds ( 700 km) of the LLSVPs have an integrated excess density of 0.60%. The detailed distribution of this buoyancy, for example whether it primarily resides in a thin layer at the base of the mantle, will require further testing and the augmentation of the inversions to include independent data sets (e.g., seismic observations). In any case, our inference of excess density requires the preservation of chemical heterogeneity associated with the enrichment of high-density chemical components, possibly linked to subducted oceanic plates and/or primordial material, in the deep mantle. This conclusion has important implications for the stability of these structures and, in turn, the history and ongoing evolution of the Earth system.

Insights into the petrogenesis of low- and high-Ti basalts: Stratigraphy and geochemistry of four lava sequences from the central Paraná basin

NASA Astrophysics Data System (ADS)

De Min, Angelo; Callegaro, Sara; Marzoli, Andrea; Nardy, Antonio J.; Chiaradia, Massimo; Marques, Leila S.; Gabbarrini, Ilaria

2018-04-01

Lava flow sequences were sampled in the central part of the Paraná basin aiming to verify the time-related evolution of the Paraná basaltic magmatism. It is shown that low- and high-Ti basalts were erupted synchronously. In particular, Esmeralda and Pitanga flows are interlayered, with the former prevailing in the upper part of the sequence. Evidence for synchronously active magma plumbing systems is also supported by mineralogical data, showing signs of mixing between the two groups. Geochemical data, including Sr-Nd-Pb isotopic compositions are furthermore used to define the mantle source of various low- (Esmeralda and Gramado) and high-Ti (Pitanga and Urubici) magma types. Involvement of a carbonatitic component is proposed for the genesis of the basalts (particularly for the Urubici ones) as suggested by trace element enrichments unrelated to significant isotopic variations. This carbonatitic signature of the mantle source may be conveyed by CO2-rich metasomatic fluids or melts percolating upwards within the sub-continental lithospheric mantle (SCLM) leading to rapid and selective enrichment of incompatible trace elements. Metasomatism was probably localized at the outskirts of the basin, were Urubici tholeiites and contemporaneous carbonatites were erupted. Geochemical data also suggest the occurrence of significant amounts of crustal contamination in the LTi magmas (mainly in the Gramado and in the late Esmeralda lavas) while crustal assimilation seems negligible in the HTi samples. Globally, a very complex picture arises for the genesis of the Paraná tholeiites, with near-synchronous and geographically coincident flows undergoing significantly different extents of interaction with the crust and tapping different mantle sources.

Crustal structure and origin of the Eggvin Bank west of Jan Mayen, NE Atlantic

NASA Astrophysics Data System (ADS)

Tan, Pingchuan; Breivik, Asbjørn Johan; Trønnes, Reidar G.; Mjelde, Rolf; Azuma, Ryosuke; Eide, Sigurd

2017-01-01

The Eggvin Bank, located between the Jan Mayen Island and Greenland, is an unusually shallow area containing several submarine volcanic peaks, confined by two transforms on the Northern Kolbeinsey Ridge (NKR). We represent P and S wave velocity models for the Eggvin Bank based on an Ocean Bottom Seismometer profile collected in 2011, showing igneous crustal thickness variations from 8 km to 13 km. A 2-5 km increase is associated with two separate 20-30 km wide segments under the main seamounts. The oceanic crust has three layers: upper crust (L2A: 2.8-4.8 km/s), middle crust (L2B: 5.5-6.5 km/s), and lower crust (L3: 6.7-7.35 km/s). Both the thick layer 2(A/B) and the high ratio of layer 2(A/B) thickness to total crustal thickness indicate that secondary, intraplate magmatism built the seamounts of the Eggvin Bank. The seamount in the north where the crust is thickest has a flat top indicating subaerial exposure but is deeper than those with rounded tops in the south and is therefore probably older. Comparing lower crustal seismic velocity with crustal thickness also indicates that the degree of mantle melting may be higher in the north than in the south. An enriched mantle source presently feeds the NKR magmatism and probably influenced the Eggvin Bank development also at earlier times. To what extent the Eggvin Bank has been influenced by the Iceland plume is uncertain, both an enriched mantle component and elevated mantle temperature may have played a role at different times and locations.

Melt inclusion evidence for a volatile-enriched (H2O, Cl, B) component in parental magmas of Gorgona Island komatiites

NASA Astrophysics Data System (ADS)

Kamenetsky, V.; Sobolev, A.; McDonough, W.

2003-04-01

Late Cretaceous komatiites of Gorgona Island are unambiguous samples of ultra-mafic melts related to a hot and possibly 'wet' mantle plume. Despite significant efforts in studying komatiites, their volatile abundances remain largely unknown because of significant alteration of rocks and lack of fresh glasses. This work presents major, trace and volatile element data for 22 partially homogenised (at 1275oC and 1 bar pressure) melt inclusions in olivine (Fo 90.5-91.5) from a Gorgona Isl. komatiite (# Gor 94-3). Major element compositions (except FeO which is notably lower by up to 5 wt% as a result of post-entrapment re-equilibration) and most lithophile trace elements of melt inclusions are indistinguishable from the whole rock komatiites. With the exception of three inclusions that have low Na, H2O, Cl, F and S (likely compromised and degassed during heating) most compositions are characterised by relatively constant and high volatile abundances (H2O 0.4-0.8 wt%, Cl 0.02-0.03 wt%, B 0.8-1.4 ppm). These are interpreted as representative of original volatiles in parental melts because they correspond to the internal volatile pressure in the closed inclusions significantly exceeding 1 bar pressure of heating experiment. Although H2O is strongly enriched (PM-normalised H2O/Ce 10-17) its concentrations correlate well with many elements (e.g. Yb, Er, Y, Ti, Sr, Be). Other positive anomalies on the overall depleted (La/Sm 0.26-0.33) PM normalized compositional spectra of melt inclusions are shown by B (B/K 2.4-5.4) and Cl (Cl/K 11-16). Compositions of melt inclusions, when corrected for Fe loss and recalculated in equilibrium with host olivine, have high MgO (15.4-16.4 wt%; Mg# of 74) and substantial H2O (0.4-0.6 wt%) contents. This together with the data on other 'enriched' elements argues for the presence of previously unknown volatile-enriched component in the parental melts of Gorgona Isl. komatiites. We discuss contamination of magmas by altered oceanic crust in the plumbing system, the involvement of volatile-rich subduction related component(s) in the mantle source, and the geochemical control from residual garnet during the generation of komatiite primary melts.

Source characteristics and tectonic setting of mafic-ultramafic intrusions in North Xinjiang, NW China: Insights from the petrology and geochemistry of the Lubei mafic-ultramafic intrusion

NASA Astrophysics Data System (ADS)

Chen, Bao-Yun; Yu, Jin-Jie; Liu, Shuai-Jie

2018-05-01

The newly discovered Lubei sulfide-bearing mafic-ultramafic intrusion forms the western extension of the Huangshan-Jin'erquan mafic-ultramafic intrusion belt in East Tianshan, NW China. The Lubei intrusion comprises hornblende peridotite, lherzolite, and harzburgite in its southern portion, gabbro in its middle portion, and hornblende gabbro in its northern portion. Intrusive relationships indicate that three magma pulses were involved in the formation of the intrusion, and that they were likely evolved from a common primitive magma. Estimated compositions of the Lubei primitive magma are similar to those of island arc calc-alkaline basalt except for the low Na2O and CaO contents of the Lubei primitive magma. This paper reports on the mineral compositions, whole-rock major and trace element contents, and Rb-Sr and Sm-Nd isotopic compositions of the Lubei intrusion, and a zircon LA-MC-ICP-MS U-Pb age for hornblende gabbro. The Lubei intrusion is characterized by enrichment in large-ion lithophile elements, depletion in high-field-strength elements, and marked negative Nb and Ta anomalies, with enrichment in chondrite-normalized light rare earth elements. It exhibits low (87Sr/86Sr)i ratios of 0.70333-0.70636 and low (143Nd/144Nd)i ratios of 0.51214-0.51260, with positive εNd values of +4.01 to +6.33. LA-ICP-MS U-Pb zircon ages yielded a weighted-mean age of 287.9 ± 1.6 Ma for the Lubei intrusion. Contemporaneous mafic-ultramafic intrusions in different tectonic domains in North Xinjiang show similar geological and geochemical signatures to the Lubei intrusion, suggesting a source region of metasomatized mantle previously modified by hydrous fluids from the slab subducted beneath the North Xinjiang region in the early Permian. Metasomatism of the mantle was dominated by hydrous fluids and was related to subduction of the Paleo-Asian oceanic lithosphere during the Paleozoic. Sr-Nd-Pb isotopic compositions suggest that the mantle source was a mixture of depleted mid-ocean-ridge-basalt mantle and enriched-mantle I components. The Permian mafic-ultramafic intrusions in North Xinjiang were formed from tholeiitic basaltic magmas derived from decompression partial melting of the metasomatized mantle in a post-collision extensional tectonic setting. The tholeiitic basaltic magmas are equivalent to the voluminous underplated basaltic magmas that formed during vertical crustal growth of the Central Asian Orogenic Belt in the later Paleozoic.

Geodynamic Implications of Himu Mantle In The Source of Tertiary Volcanics From The Veneto Region (south Eastern Alps)

NASA Astrophysics Data System (ADS)

Macera, P.; Gasperini, D.; Blichert-Toft; Bosch, D.; del Moro, A.; Dini, G.; Martin, S.; Piromallo, C.

DuringTertiary times extensive mafic volcanism took place in the South-Eastern Alps, along a half-graben structure bounded by the Schio-Vicenza main fault. This mag- matism gave rise to four main volcanic centers: Lessini, Berici, Euganei, and Maros- tica. The dominating rock types are alkali basalts, basanites and transitional basalts, with hawaiites, trachybasalts, tephrites, basaltic andesites, and differentiated rocks be- ing less common. Major and trace element and Sr-Nd-Hf-Pb isotopic data for the most primitive lavas from each volcanic center show the typical features of HIMU hotspot volcanism, variably diluted by a depleted asthenospheric mantle component (87Sr/86Sr48Ma = 0.70314-0.70321; eNd48Ma = +6.4 to +6.5; eHf48Ma = +6.4 to +8.1, 206Pb/204Pb48Ma = 18.786-19.574). Since the HIMU component is consid- ered to be of deep mantle origin, its presence in a tectonic environment dominated by subduction (the Alpine subduction of the European plate below the Adria plate) has significant geodynamic implications. Slab detachment and ensuing rise of deep man- tle material into the lithospheric gap is proposed to be a viable mechanism of hotspot magmatism in a subduction zone setting. Interaction between deep-seated plume ma- terial and shallow depleted asthenospheric mantle may account for the geochemical features of the Veneto volcanics, as well as those of the so-called enriched astheno- spheric reservoir (EAR) component. Ascending counterflow of deep mantle material through the lithospheric gap to the top of the subducting slab further may induce heat- ing of the overriding plate and trigger it to partially melt. Upwelling of the resulting mafic magmas and their subsequent underplating at the mantle-lower crust bound- ary would favor partial melting of the lower crust, thereby giving rise to the bimodal mafic-felsic magmatism that characterizes the whole Periadriatic province. According to this model, the HIMU-like magmatism of the Alpine foreland is therefore closely related to the calc-alkaline magmatism of the Periadriatic Lineament, and caused by the same mechanism of Tertiary Alpine convergence tectonics.

The isotopic and chemical evolution of Mount St. Helens

USGS Publications Warehouse

Halliday, A.N.; Fallick, A.E.; Dickin, A.P.; Mackenzie, A.B.; Stephens, W.E.; Hildreth, W.

1983-01-01

Isotopic and major and trace element analysis of nine samples of eruptive products spanning the history of the Mt. St. Helens volcano suggest three different episodes; (1) 40,000-2500 years ago: eruptions of dacite with ??{lunate}Nd = +5, ??{lunate}Sr = -10, variable ??18O, 206Pb/204Pb ??? 18.76, Ca/Sr ??? 60, Rb/Ba ??? 0.1, La/Yb ??? 18, (2) 2500-1000 years ago: eruptions of basalt, andesite and dacite with ??{lunate}Nd = +4 to +8, ??{lunate}Sr = -7 to -22, variable ??18O (thought to represent melting of differing mantle-crust reservoirs), 206Pb/204Pb = 18.81-18.87, variable Ca/Sr, Rb/Ba, La/Yb and high Zr, (3) 1000 years ago to present day: eruptions of andesite and dacite with ??{lunate}Nd = +6, ??{lunate}Sr = -13, ??18O ???6???, variable 206Pb/204Pb, Ca/Sr ??? 77, Rb/Ba = 0.1, La/Yb ??? 11. None of the products exhibit Eu anomalies and all are LREE enriched. There is a strong correlation between 87Sr/86Sr and differentiation indices. These data are interpreted in terms of a mantle heat source melting young crust bearing zircon and garnet, but not feldspar, followed by intrusion of this crustal reservoir by mantle-derived magma which caused further crustal melting and contaminated the crustal magma system with mafic components. Since 1000 years ago all the eruptions have been from the same reservoir which has displayed a much more gradual re-equilibration of Pb isotopic compositions than other components suggesting that Pb is being transported via a fluid phase. The Nd and Sr isotopic compositions lie along the mantle array and suggest that the mantle underneath Mt. St. Helens is not as depleted as MORB sources. There is no indication of seawater involvement in the source region. ?? 1983.

The Mineralogical Record of Oxygen Fugacity Variation and Alteration in Northwest Africa 8159: Evidence for Interaction Between a Mantle Derived Martian Basalt and a Crustal Component(s)

NASA Technical Reports Server (NTRS)

Shearer, Charles K.; Burger, Paul V.; Bell, Aaron S.; McCubbin, Francis M.; Agee, Carl; Simon, Justin I.; Papike, James J.

2015-01-01

A prominent geochemical feature of basaltic magmatism on Mars is the large range in initial Sr isotopic ratios (approx. 0.702 - 0.724) and initial epsilon-Nd values (approx. -10 to greater than +50). Within this range, the shergottites fall into three discreet subgroups. These subgroups have distinct bulk rock REE patterns, mineral chemistries (i.e. phosphate REE patterns, Ni, Co, V in olivine), oxygen fugacity of crystallization, and stable isotopes, such as O. In contrast, nakhlites and chassignites have depleted epsilon-Nd values (greater than or equal to +15), have REE patterns that are light REE enriched, and appear to have crystallized near the FMQ buffer. The characteristics of these various martian basalts have been linked to different reservoirs in the martian crust and mantle, and their interactions during the petrogenesis of these magmas. These observations pose interesting interpretive challenges to our understanding of the conditions of the martian mantle (e.g. oxygen fugacity) and the interaction of mantle derived magmas with the martian crust and surface. Martian meteorite NWA 8159 is a unique fine-grained augite basalt derived from a highly depleted mantle source as reflected in its initial epsilon-Nd value, contains a pronounced light REE depleted pattern, and crystallized presumably under very oxidizing conditions. Although considerably older than both shergottites and nahklites, it has been petrogenetically linked to both styles of martian magmatism. These unique characteristics of NWA 8159 may provide an additional perspective for deciphering the petrogenesis of martian basalts and the nature of the crust of Mars.

Plume versus plate origin for the Shatsky Rise oceanic plateau (NW Pacific): Insights from Nd, Pb and Hf isotopes

NASA Astrophysics Data System (ADS)

Heydolph, Ken; Murphy, David T.; Geldmacher, Jörg; Romanova, Irina V.; Greene, Andrew; Hoernle, Kaj; Weis, Dominique; Mahoney, John

2014-07-01

Shatsky Rise, an early Cretaceous igneous oceanic plateau in the NW Pacific, comprises characteristics that could be attributed to either formation by shallow, plate tectonic-controlled processes or to an origin by a mantle plume (head). The plateau was drilled during Integrated Ocean Drilling Program (IODP) Expedition 324. Complementary to a recent trace element study (Sano et al., 2012) this work presents Nd, Pb and Hf isotope data of recovered lava samples cored from the three major volcanic edifices of the Shatsky Rise. Whereas lavas from the oldest edifice yield fairly uniform compositions, a wider isotopic spread is found for lavas erupted on the younger parts of the plateau, suggesting that the Shatsky magma source became more heterogeneous with time. At least three isotopically distinct components can be identified in the magma source: 1) a volumetrically and spatially most common, moderately depleted component of similar composition to modern East Pacific Ridge basalt but with low 3He/4He, 2) an isotopically very depleted component which could represent local, early Cretaceous (entrained) depleted upper mantle, and 3) an isotopically enriched component, indicating the presence of (recycled) continental material in the magma source. The majority of analyzed Shatsky lavas, however, possess Nd-Hf-Pb isotope compositions consistent with a derivation from an early depleted, non-chondritic reservoir. By comparing these results with petrological and trace element data of mafic volcanic rock samples from all three massifs (Tamu, Ori, Shirshov), we discuss the origin of Shatsky Rise magmatism and evaluate the possible involvement of a mantle plume (head).

Silicon Isotope Geochemistry of Ocean Island Basalts: Search for Deep Mantle Heterogeneities and Evidence for Recycled Altered Oceanic Crust

NASA Astrophysics Data System (ADS)

Pringle, E. A.; Savage, P. S.; Jackson, M. G.; Moreira, M. A.; Day, J. M.; Moynier, F.

2014-12-01

Analyses of Ocean Island Basalts (OIB) have shown that the Earth's mantle contains isotopically distinct components, but debate about the degree and cause of variability persists. The study of silicon (Si) isotopes in OIBs has the potential to elucidate mantle heterogeneities. Relatively large (~several per mil) Si isotopic fractionation occurs in low-temperature environments during precipitation from dissolved Si, where the precipitate is preferentially enriched in the lighter isotopes [1], but only a limited range (~tenths of a per mil) of Si isotope fractionation has been observed due to high-temperature igneous processes [2]. Therefore, Si isotopes may be useful as tracers for the presence of crustal material in OIB source regions in a manner similar to more conventional stable isotope systems, such as oxygen. Here we present the first comprehensive suite of high-precision Si isotopic data obtained by MC-ICP-MS for a diverse set of OIBs representing the EM-1, EM-2, and HIMU mantle components. In general, the Si isotopic compositions of OIBs analyzed here are agreement with previous estimates for Bulk Silicate Earth (BSE). However, small systematic variations are present; the HIMU end-member Mangaia and HIMU-type Cape Verde island São Nicolau are enriched in the light isotopes of Si (δ30Si = -0.37 ± 0.06‰ and δ30Si = -0.39 ± 0.04‰, respectively; errors are 2sd), with compositions intermediary between Mid Ocean Ridge Basalts and chondritic values. Additionally, Iceland samples from volcanic complexes in the Northern Rift Zone show similar Si isotope compositions (on average, δ30Si = -0.40 ± 0.06‰). In contrast, the δ30Si averages of the EM-1 end-member Pitcairn (-0.28 ± 0.07‰), the EM-2 end-member Samoa (-0.31 ± 0.07‰) and other OIB localities do not show any significant difference from previous estimates for the δ30Si value of BSE [3]. The Si isotopic variability in some HIMU-type and Icelandic OIBs most likely reflects the incorporation of recycled altered oceanic crust in the plume source. However, the sampling of a primitive reservoir enriched in the light isotopes of Si, as suggested by [4], cannot be ruled out as a potential source of Si isotope variations in OIBs. References: [1] Ziegler et al., GCA 2005 [2] Savage et al., GCA 2011 [3] Savage et al., EPSL 2010 [4] Huang et al., GCA 2014

Titanium Isotopes Link the High 3He/4He Reservoir to Continent Formation

NASA Astrophysics Data System (ADS)

Millet, M. A.; Jackson, M. G.; Dauphas, N.; Burton, K. W.; Williams, H. M.; Kurz, M. D.; Doucelance, R.; Smithies, H.; Champion, D. C.; Nowell, G. M.

2016-12-01

Elevated 3He/4He ratios found in ocean island basalts (OIB) argue for the survival of an early-formed reservoir (>4.5 Ga) in the Earth's mantle [1]. However, its nature remains debated. A characteristic of high 3He/4He OIBs is their anomalous enrichment in Ti abundance relative to elements of similar incompatibility (Sm and Tb). Here we use a new geochemical tool, the stable isotopes of Titanium, to investigate the origin of Ti enrichment of high 3He/4He OIBs. Recent work [2] has shown that Ti isotopes are a powerful tracer of oxide-melt equilibrium in magmatic systems. Results show that primitive OIB samples from localities associated with low 3He/4He ratios (≤15 R/Ra) have δ49Ti values within error of the mantle (δ49Ti=0.005±0.005 [2]) and chondrite values (+0.004±0.010 [3]) regardless of their Ti anomaly (0.93He/4He ratios (>25R/Ra) display δ49Ti values ranging from mantle-like to enriched in light isotopes (up to -0.065‰±0.005) that are negatively correlated with their Ti/Ti* and uncorrelated to indices of magma differentiation. This indicates that i) elevated Ti/Ti* in high 3He/4He OIBs is a mantle source signature and ii) that the high 3He/4He reservoir is enriched in light isotopes of Ti relative to the BSE. This enrichment in light isotopes is balanced by the heavy δ49Ti values and negative Ti/Ti* of Archean Tonalite-Throndhjemite-Granodiorite samples (TTG) from the Pilbara and Yilgarn Craton (+0.20<δ49Ti<+0.40), a proxy for early-formed, juvenile continental crust. Given the chondritic composition of the Earth's mantle and the inability of the typical mantle lithologies to fractionate Ti isotopes, this implies that the Ti enrichment of the high 3He/4He mantle reservoir is linked to the recycling of residues of partial melting events in the presence of rutile (TiO2), a process that drove continent formation in the Archean and possibly earlier. In addition, since these residues cannot display elevated 3He/4He ratios, it requires the Ti-He signature of the high 3He/4He reservoir is due to recycling of entire slab packages. [1] Rizo et al., Science, 2016 [2] Millet et al., EPSL, 2016 [3] Greber et al., LPSC, 2016

Mantle transition zone-derived EM1 component beneath NE China: Geochemical evidence from Cenozoic potassic basalts

NASA Astrophysics Data System (ADS)

Wang, Xiao-Jun; Chen, Li-Hui; Hofmann, Albrecht W.; Mao, Fu-Gen; Liu, Jian-Qiang; Zhong, Yuan; Xie, Lie-Wen; Yang, Yue-Heng

2017-05-01

The isotopic characteristics of the sub-oceanic mantle are well established, but in continental regions these properties are usually obscured, and therefore controversial, because of the potential effects of crustal contamination together with lithospheric mantle metasomatism and melting. The so-called EM1 (Enriched Mantle-1) signature, characterized by low 206Pb/204Pb and 143Nd/144Nd ratios, is particularly problematic in this respect because EM1-type OIB sources are commonly attributed to recycled crust and/or lithospheric mantle. In this paper we show that a suite of Cenozoic potassic basalts from NE China displays many previously unrecognized correlations between chemical and isotopic parameters, which tightly constrain the isotopic characteristics of an extreme EM1-type mantle source located in the asthenosphere. Its radiogenic isotopes are similar to, but even more extreme than, those of the oceanic endmember composition represented by the Pitcairn hotspot, namely 206Pb/204Pb ≤ 16.5, 143Nd/144Nd ≤ 0.5123 (or εNd ≤ - 6.4), 176Hf/177Hf ≤ 0.2825 (or εHf ≤ - 10.1). These characteristics require a source of recycled crustal material of Precambrian age (∼2.2 Ga). An important new constraint is the Mg isotopic composition of δ26 Mg (≤ - 0.6 ‰), which is lower than normal mantle (δ26 Mg = - 0.25 ± 0.07 ‰) and lower crustal values (δ26 Mg = - 0.29 ± 0.15 ‰), but consistent with sedimentary carbonate (δ26 Mg = - 5.57 ‰ to - 0.38 ‰). The endmember EM1 source produced high-SiO2 melts with low MgO, CaO/Al2O3 and δ26 Mg values, exceptionally high K/U ≅ 50,000, Ba/Th ≅ 400, low U/Pb ≅ 0.06, and positive Zr and Hf anomalies. The chemical and isotopic parameters of this potassic basalt suite form binary mixing arrays, one end point of which is the inferred asthenospheric EM1 reservoir, whereas the other is a more ordinary, depleted mantle component, which is also sampled by local lithospheric mantle xenoliths. These binary arrays include well-developed correlations between Sr, Nd, Hf, Pb and Mg isotopes, negative correlations of 206Pb/204Pb with K2 O, K/U, Hf/Hf*, positive correlations of δ26 Mg with MgO, and 143Nd/144Nd with Fe2OT3 and U/Pb. We propose that the EM1 reservoir contains recycled ancient carbonate-bearing sediments, subducted into the mantle transition zone, where K, Rb, Ba and Pb are sequestered by K-hollandite as suggested by Murphy et al. (2002) for the Gaussberg lamproites. Loss of small amounts of carbonate melt extracted Th, U and some of the LREE, while retaining K, Rb, Ba, Pb, Zr and Hf in the residue, thereby generating the observed trace element anomalies. In Cenozoic time, this deep EM1 reservoir ascended into the shallow asthenosphere and underwent low-degree partial melting, at pressures below the stability field of K-hollandite, thereby releasing K, Rb and Ba into the melt. The partial melts ascended through subcontinental lithosphere and were progressively modified by interaction with the lithospheric mantle, thus accounting for the linear chemical and isotopic trends noted above. This interaction imposed a progressively more depleted character on the erupted melt, both in terms of isotopic composition and trace element enrichment.

Picrite "Intelligence" from the Middle-Late Triassic Stikine arc: Composition of mantle wedge asthenosphere

NASA Astrophysics Data System (ADS)

Milidragovic, D.; Zagorevski, A.; Weis, D.; Joyce, N.; Chapman, J. B.

2018-05-01

Primitive, near-primary arc magmas occur as a volumetrically minor ≤100 m thick unit in the Canadian Cordillera of northwestern British Columbia, Canada. These primitive magmas formed an olivine-phyric, picritic tuff near the base of the Middle-Late Triassic Stuhini Group of the Stikine Terrane (Stikinia). A new 40Ar/39Ar age on hornblende from a cross-cutting basaltic dyke constrains the tuff to be older than 221 ± 2 Ma. An 87Sr/86Sr isochron of texturally-unmodified tuff samples yields 212 ± 25 Ma age, which is interpreted to represent syn-depositional equilibration with sea-water. Parental trace element magma composition of the picritic tuff is strongly depleted in most incompatible trace elements relative to MORB and implies a highly depleted ambient arc mantle. High-precision trace element and Hf-Nd-Pb isotopic analyses indicate an origin by mixing of a melt of depleted ambient asthenosphere with ≤2% of subducted sediment melt. Metasomatic addition of non-conservative incompatible elements through melting of subducted Panthalassa Ocean floor sediments accounts for the arc signature of the Stuhini Group picritic tuff, enrichment of light rare earth elements (LREE) relative to heavy rare earth elements (HREE) and high field strength elements (HFSE), and anomalous enrichment in Pb. The inferred Panthalassan sediments are similar in composition to the Neogene-Quaternary sediments of the modern northern Cascadia Basin. The initial Hf isotopic composition of the picritic tuff closely approximates that of the ambient Middle-Late Triassic asthenosphere beneath Stikinia and is notably less radiogenic than the age-corrected Hf isotopic composition of the Depleted (MORB) Mantle reservoir (DM or DMM). This suggests that the ambient asthenospheric mantle end-member experienced melt depletion (F ≤ 0.05) a short time before picrite petrogenesis. The mantle end-member in the source of the Stuhini Group picritic tuff is isotopically similar to the mantle source of enriched mid-ocean ridge basalts (E-MORB) erupted today at the southern end of the Explorer Ridge in northeastern Pacific Ocean. The isotopic similarity between the Middle-Late Triassic ambient mantle under Stikinia, and mantle presently tapped at the southern Explorer Ridge suggests that enriched domains in the northeastern Pacific mantle are long-lived (≥222 million years).

Trace Element Study of MORB Glasses from 14¡ã-16¡ãN along Mid-Atlantic Ridge by LA-ICP- MS

NASA Astrophysics Data System (ADS)

Barzoi, C. A.; Casey, J. F.; Gao, Y.; Lapen, T.

2007-12-01

A comparison of 20 MORB glasses from 14°-16° N along the Mid-Atlantic Ridge using both solution-based and in situ laser ablation-based ICP-MS trace element analyses on the same samples was conducted. Li, Be, Sc, Ti, V, Cr, Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Ba, La, Ce, Pr, Nd, Sm, Eu, Tb, Gd, Dy, Ho, Er, Tm, Yb,Lu, Hf, Ta, Pb, Th, and U were analyzed using the Varian 810 quadrupole ICP-MS. The instrument features a 90 degree ion mirror and low noise double-off-axis quadrupole that allows high sensitivity and low backgrounds. Precision in term of relative standard deviation (RSD) of the measurements for both methods based on repeated analyses of USGS BIR-1G and BHVO-2G glass standards and Max Planck KL-2G glass standard is within 5 % for all trace elements with the exception of Pb, which averaged 12 %. Measured trace element abundances are within 2% of recommended standard values using both solution and laser ablation methods. Comparison between the analyte concentrations obtained by solution-based ICP-MS and in situ microanalysis by laser ablation reveals little systematic differences in abundances(<5% for all elements). The two-method correlation and strong repeatability of the results indicate that rapid in situ trace element analysis by laser ablation ICP-MS is likely to become a preferred method of trace element analysis for MORB glasses. Our geochemical results and previous studies of MORB glasses in the region of the MAR between 14°-16°N show that basalts are characterized isotopic and incompatible element enrichment.The nature of the enrichment has been the topic of significant discussion and speculation because a specific mantle plume is not well defined in the region. Likewise the magma supply is probably small in the region as the magmatic crust is interpreted to be very thin in most of the area studied. Integrated studies of major element, trace element, and isotopic variations among basalts, gabbroic rocks and igneous and residual ultramafic rocks in the region indicate that 1) the enriched basalts have positive Ta-Nb anomalies, enriched relative to U, Th, and La 2) basalts have relatively high SiO2 abundances compared to the global average, 3) basalts show a HIMU isotopic signature, and 4) bulk major element abundances and mineral chemistry in mantle rocks indicate that they are among the most depleted,although variably refertilized, residual mantle assemblages sampled to date along MORs.We suggest that much of the regional variation in major and trace element data, as well as isotopic data and the unusual regional geology (multiple core complexes) can be explained by melting of a sub-axial mantle that contains two end members, one highly depleted and the other enriched. These components appear to involve ancient recycled ocean crust and lithospheric mantle.

Helium in the Archaean komatiites revisited: significantly high 3He/4He ratios revealed by fractional crushing gas extraction

NASA Astrophysics Data System (ADS)

Matsumoto, T.; Seta, A.; Matsuda, J.; Chen, Y.; Arai, S.

2001-12-01

In order to provide constraints on 3He/4He ratios in the Archaean mantle source, we have analysed helium isotopic compositions in 2.7Ga old Archaean komatiites from the Abitibi green stone belt, Ontario, Canada. Two spinifex-textured komatiites yielded significantly high 3He/4He ratios of about 30Ra (where Ra denotes the atmospheric 3He/4He ratio) in fractions released by sequential crushing. These results are the first confirmation of the occurrence of high 3He/4He component in Archaean komatiites after the intriguing finding by [Richard et al., Science 273 (1996) 93-95] in komatiites from a nearby locality, Alexo. We also found that the crystal structure of the komatiites was significantly enriched in a radiogenic component (4He) and that the radiogenic 4He in the crystal structure was actually degassed by a crushing gas extraction, indicating that the nominal 3He/4He ratios measured by crushing are lower limits for the 3He/4He ratio of an intrinsic component. By constraining the release behaviour of radiogenic 4He by crushing, we have estimated the initial 3He/4He ratio of an inclusion-trapped component to be 73 (+7.8/-5.5) Ra. A mantle source with such a high 3He/4He ratio at 2.7Ga would, if evolved in a closed-system, have present-day 3He/4He ratio of 46-60Ra, indicating that the komatiites from Munro had been trapped their helium from a mantle reservoir with very high 3He/4He ratio in the context of the present-day value. However, whether or not such a source can be considered as the one that is equivalent to the primitive mantle source (such that sampled at hotspots) is highly model-dependent. If a closed-system evolution model were assumed, helium in the Munro komatiites is not likely to be derived from the MORB-source-like reservoir. However, the notion that the komatiites may be derived from a depleted reservoir in terms of trace elemental and isotopic geochemistry might requires an alternative view for the evolution of 3He/4He ratio in ancient mantle reservoirs, as has been demonstrated by a recent model calculation by [Seta et al., Earth Planet. Sci. Lett. 188 (2001) 211-219] in which the 3He/4He ratios in the MORB mantle source could have been as high as those in the primitive (less-degassed) mantle source in Archaean.

Assessment of the Interstellar Processes Leading to Deuterium Enrichment in Meteoritic Organics

NASA Technical Reports Server (NTRS)

Sandford, Scott A.; Bernstein, Max P.; Dworkin, Jason P.; DeVincenzi, Donald L. (Technical Monitor)

2001-01-01

The presence of isotopic anomalies is the most unequivocal demonstration that meteoritic material contains circumstellar or interstellar components. In the case of organic compounds in meteorites and interplanetary dust particles (IDPs), the most useful isotopic tracer has been deuterium (D). We discuss four processes that are expected to lead to D enrichment in interstellar materials and describe how their unique characteristics can be used to assess their relative importance for the organics in meteorites. These enrichment processes are low temperature gas phase ion-molecule reactions, low temperature gas-grain reactions, gas phase unimolecular photodissociation, and ultraviolet photolysis in D-enriched ice mantles. Each of these processes is expected to be associated with distinct regiochemical signatures (D placement on the product molecules, correlation with specific chemical functionalities, etc.), especially in the molecular population of polycyclic aromatic hydrocarbons (PAHs). We describe these differences and discuss how they may be used to delineate the various interstellar processes that may have contributed to meteoritic D enrichments. We also briefly discuss how these processes may affect the isotopic distributions in C, 0, and N in the same compounds.

Noble gases in CH 4-rich gas fields, Alberta, Canada

NASA Astrophysics Data System (ADS)

Hiyagon, H.; Kennedy, B. M.

1992-04-01

The elemental and isotopic compositions of helium, neon, argon, and xenon in twenty-one CH 4-rich natural gas samples from Cretaceous and Devonian reservoirs in the Alberta, Canada, sedimentary basin were measured. In all but a few cases, radiogenic ( 4He, 40Ar, and 131-136Xe) and nucleogenic ( 21,22Ne) isotopes dominated. Based solely on the noble gas composition, two types of natural gas reservoirs are identified. One (Group B) is highly enriched in radiogenic-nucleogenic noble gases and varies little in composition: 3He /4He = 1.5 ± 0.5 × 10 -8, 40Ar /36Ar = 5000-6500 , 40∗Ar /4He = 0.10 , 136∗Xe /4He ~ 0.7 × 10 -9, and 21∗Ne /22∗Ne = 0.452 ± 0.041 (∗ denotes radiogenic or nucleogenic origin; all 4He is radiogenic). High nitrogen content with 4He /N 2 ~ 0.06 is also characteristic of Group B samples. The remaining samples (Group A) contain a radiogenic-nucleogenic component with a different composition and, relative to Group B samples, the extent of enrichment in this component is less and more variable: 3He /4He = 10-70 × 10 -8, 40Ar /36Ar < 1550 , and 40∗Ar /4He ~ 0.25 . The composition of Group B radiogenic-nucleogenic noble gases is consistent with production in crust of average composition. Enrichment in Group B noble gases and nitrogen increases with proximity to the underlying Precambrian basement, consistent with a present-day mass flux into the overlying sedimentary basin. Inferred 40∗Ar /136∗Xe 4He ratios imply a basement source enriched in thorium relative to uranium and potassium (Th/U > 20). Combined, the overall lower total radiogenic-nucleogenic content of Group A reservoirs, the greater variability in composition, and the appearance of Group A noble gases in reservoirs higher in the sedimentary sequence relative to the underlying basement implies that the Group A radiogenic-nucleogenic noble gases are indigenous to the sediments. The most interesting aspect of the Group A noble gases are the very high 3He /4He ratios; ~ 10-70 times greater than expected if derived from average crust. The mantle, surface cosmogenic 3He production, cosmic dust, or production in a lithium-enriched environment as potential sources for the 3He excesses are evaluated. The present data set would seem to rule out cosmogenic 3He. The mantle, cosmic dust, or high Li, however, remain viable candidates. The relative abundances of the nonradiogenic, non-nucleogenic noble gases show no correlation with the Group A-B reservoir classification. Compositional variations indicate three-component mixing between air or an air-like component, 10°C air-saturated water, and a third component enriched in xenon. Apparently, the latter cannot be derived from equilibrium solubility degassing of air-saturated water or oil-water mixtures, and may have been derived from devolatilization of C-rich petroleum source sediments.

Geochemistry of continental subduction-zone fluids

NASA Astrophysics Data System (ADS)

Zheng, Yong-Fei; Hermann, Joerg

2014-12-01

The composition of continental subduction-zone fluids varies dramatically from dilute aqueous solutions at subsolidus conditions to hydrous silicate melts at supersolidus conditions, with variable concentrations of fluid-mobile incompatible trace elements. At ultrahigh-pressure (UHP) metamorphic conditions, supercritical fluids may occur with variable compositions. The water component of these fluids primarily derives from structural hydroxyl and molecular water in hydrous and nominally anhydrous minerals at UHP conditions. While the breakdown of hydrous minerals is the predominant water source for fluid activity in the subduction factory, water released from nominally anhydrous minerals provides an additional water source. These different sources of water may accumulate to induce partial melting of UHP metamorphic rocks on and above their wet solidii. Silica is the dominant solute in the deep fluids, followed by aluminum and alkalis. Trace element abundances are low in metamorphic fluids at subsolidus conditions, but become significantly elevated in anatectic melts at supersolidus conditions. The compositions of dissolved and residual minerals are a function of pressure-temperature and whole-rock composition, which exert a strong control on the trace element signature of liberated fluids. The trace element patterns of migmatic leucosomes in UHP rocks and multiphase solid inclusions in UHP minerals exhibit strong enrichment of large ion lithophile elements (LILE) and moderate enrichment of light rare earth elements (LREE) but depletion of high field strength elements (HFSE) and heavy rare earth elements (HREE), demonstrating their crystallization from anatectic melts of crustal protoliths. Interaction of the anatectic melts with the mantle wedge peridotite leads to modal metasomatism with the generation of new mineral phases as well as cryptic metasomatism that is only manifested by the enrichment of fluid-mobile incompatible trace elements in orogenic peridotites. Partial melting of the metasomatic mantle domains gives rise to a variety of mafic igneous rocks in collisional orogens and their adjacent active continental margins. The study of such metasomatic processes and products is of great importance to understanding of the mass transfer at the slab-mantle interface in subduction channels. Therefore, the property and behavior of subduction-zone fluids are a key for understanding of the crust-mantle interaction at convergent plate margins.

Enrichment of trace elements in garnet amphibolites from a paleo-subduction zone: Catalina Schist, southern California

USGS Publications Warehouse

Sorensen, Sorena S.; Grossman, J.N.

1989-01-01

The abundance, P-T stability, solubility, and element-partitioning behavior of minerals such as rutile, garnet, sphene, apatite, zircon, zoisite, and allanite are critical variables in models for mass transfer from the slab to the mantle wedge in deep regions of subduction zones. The influence of these minerals on the composition of subduction-related magmas has been inferred (and disputed) from inverse modelling of the geochemistry of island-arc basalt, or by experiment. Although direct samples of the dehydration + partial-melting region of a mature subduction zone have not been reported from subduction complexes, garnet amphibolites from melanges of circumpacific and Caribbean blueschist terranes reflect high T (>600??C) conditions in shallower regions. Such rocks record geochemical processes that affected deep-seated, high-T portions of paleo-subduction zones. In the Catalina Schist, a subduction-zone metamorphic terrane of southern California, metasomatized and migmatitic garnet amphibolites occur as blocks in a matrix of meta-ultramafic rocks. This mafic and ultramafic complex may represent either slab-derived material accreted to the mantle wedge of a nascent subduction zone or a portion of a shear zone closely related to the slab-mantle wedge contact, or both. The trace-element geochemistry of the complex and the distribution of trace elements among the minerals of garnet amphibolites were studied by INAA, XRF, electron microprobe, and SEM. In order of increasing alteration from a probable metabasalt protolith, three common types of garnet amphibolite blocks in the Catalina Schist are: (1) non-migmatitic, clinopyroxene-bearing blocks, which are compositionally similar to MORB that has lost an albite component; (2) garnet-amphibolite blocks, which have rinds that reflect local interaction between metabasite, metaperidotite, and fluid; and (3) migmatites that are extremely enriched in Th, HFSE, LREE, and other trace elements. These trace-element enrichments are mineralogically controlled by rutile, garnet, sphene, apatite, zircon, zoisite, and allanite. Alkali and alkaline earth elements are much less enriched in the solid assemblage, and thus appear to be decoupled from the other elements in the inferred metasomatic process(es). The compositions of migmatitic garnet amphibolite blocks seem to complement that of "average" island-arc tholeiite. Trace-element metasomatism reflects fluid-solid, rather than melt-solid, interaction. The metasomatic effects indicate that H2O-rich fluid, perhaps with a significant component of Na-Al silicate and alkalis, carried Th, U, Sr, REE, and HFSE. Fractionations of LREE in migmatites resemble those of migmatitic metasedimentary rocks underlying the mafic and ultramafic complex. "Exotic" LREE deposited in allanite in migmatites could have been derived from fluids in equilibrium with subducted sediment. If the paleo-subduction zone represented by the mafic and ultramafic complex of the Catalina Schist had continued its thermal and fluid evolution, a selvage of similarly enriched rocks might have been generated along the slab-mantle wedge contact between ~30 and 85 km depth. Rocks affected by "subduction-zone metasomatism," although rarely recognized at the surface, could be volumetrically significant products of the initiation of subduction and may prove to be geochemical probes of convergent margins that approach the significance of xenoliths in the study of other magmatic environments. ?? 1989.

Mantle helium along the Newport-Inglewood fault zone, Los Angeles basin, California: A leaking paleo-subduction zone

NASA Astrophysics Data System (ADS)

Boles, J. R.; Garven, G.; Camacho, H.; Lupton, J. E.

2015-07-01

Mantle helium is a significant component of the helium gas from deep oil wells along the Newport-Inglewood fault zone (NIFZ) in the Los Angeles (LA) basin. Helium isotope ratios are as high as 5.3 Ra (Ra = 3He/4He ratio of air) indicating 66% mantle contribution (assuming R/Ra = 8 for mantle), and most values are higher than 1.0 Ra. Other samples from basin margin faults and from within the basin have much lower values (R/Ra < 1.0). The 3He enrichment inversely correlates with CO2, a potential magmatic carrier gas. The δ13C of the CO2 in the 3He rich samples is between 0 and -10‰, suggesting a mantle influence. The strong mantle helium signal along the NIFZ is surprising considering that the fault is currently in a transpressional rather than extensional stress regime, lacks either recent magma emplacement or high geothermal gradients, and is modeled as truncated by a proposed major, potentially seismically active, décollement beneath the LA basin. Our results demonstrate that the NIFZ is a deep-seated fault directly or indirectly connected with the mantle. Based on a 1-D model, we calculate a maximum Darcy flow rate q ˜ 2.2 cm/yr and a fault permeability k ˜ 6 × 10-17 m2 (60 microdarcys), but the flow rates are too low to create a geothermal anomaly. The mantle leakage may be a result of the NIFZ being a former Mesozoic subduction zone in spite of being located 70 km west of the current plate boundary at the San Andreas fault.

Fluid-related inclusions in Alpine high-pressure peridotite reveal trace element recycling during subduction-zone dehydration of serpentinized mantle (Cima di Gagnone, Swiss Alps)

NASA Astrophysics Data System (ADS)

Scambelluri, Marco; Pettke, Thomas; Cannaò, Enrico

2015-11-01

Serpentinites release at sub-arc depths volatiles and several fluid-mobile trace elements found in arc magmas. Constraining element uptake in these rocks and defining the trace element composition of fluids released upon serpentinite dehydration can improve our understanding of mass transfer across subduction zones and to volcanic arcs. The eclogite-facies garnet metaperidotite and chlorite harzburgite bodies embedded in paragneiss of the subduction melange from Cima di Gagnone derive from serpentinized peridotite protoliths and are unique examples of ultramafic rocks that experienced subduction metasomatism and devolatilization. In these rocks, metamorphic olivine and garnet trap polyphase inclusions representing the fluid released during high-pressure breakdown of antigorite and chlorite. Combining major element mapping and laser-ablation ICP-MS bulk inclusion analysis, we characterize the mineral content of polyphase inclusions and quantify the fluid composition. Silicates, Cl-bearing phases, sulphides, carbonates, and oxides document post-entrapment mineral growth in the inclusions starting immediately after fluid entrapment. Compositional data reveal the presence of two different fluid types. The first (type A) records a fluid prominently enriched in fluid-mobile elements, with Cl, Cs, Pb, As, Sb concentrations up to 103 PM (primitive mantle), ∼102 PM Tl, Ba, while Rb, B, Sr, Li, U concentrations are of the order of 101 PM, and alkalis are ∼2 PM. The second fluid (type B) has considerably lower fluid-mobile element enrichments, but its enrichment patterns are comparable to type A fluid. Our data reveal multistage fluid uptake in these peridotite bodies, including selective element enrichment during seafloor alteration, followed by fluid-rock interaction along with subduction metamorphism in the plate interface melange. Here, infiltration of sediment-equilibrated fluid produced significant enrichment of the serpentinites in As, Sb, B, Pb, an enriched trace element pattern that was then transferred to the fluid released at greater depth upon serpentine dehydration (type A fluid). The type B fluid hosted by garnet may record the composition of the chlorite breakdown fluid released at even greater depth. The Gagnone study-case demonstrates that serpentinized peridotites acquire water and fluid-mobile elements during ocean floor hydration and through exchange with sediment-equilibrated fluids in the early subduction stages. Subsequent antigorite devolatilization at subarc depths delivers aqueous fluids to the mantle wedge that can be prominently enriched in sediment-derived components, potentially triggering arc magmatism without the need of concomitant dehydration/melting of metasediments or altered oceanic crust.

Alkaline lavas from southern Mendoza, Argentina, extend the Patagonian DUPAL mantle field to the north

NASA Astrophysics Data System (ADS)

Soager, N.; Holm, P. M.; Llambias, E.

2010-12-01

The lavas sampled around Río Colorado ~37°S at the border of Mendoza and Neuquén provinces, Argentina, define an OIB-like end-member composition for the Pleistocene and Holocene activity in the Payún Matrú volcanic field. Although positioned in the far back-arc of the Andes, only a few lavas show signs of involvement of slab fluids or crustal contamination such as relatively high LILEs relative to Nb. The very low La/Nb (~0.66) and Zr/Nb (~5) and high U/Pb (0.3-0.4) of the end-member composition clearly distinguish the source from normal MORB mantle, while high Ba/Nb (~10) and K/Nb (370-400) compared to FOZO and HIMU type OIBs suggest an EM type of mantle. Overall, the trace element patterns of the Río Colorado lavas are similar to the central and north Patagonian intraplate basalts and to South Atlantic E-MORB affected by the Discovery plume and the LOMU component (le Roux et al., 2002, EPSL 203). The isotopic composition of the Río Colorado component has a 206Pb/204Pb = 18.4, 207Pb/204Pb = 15.58, 208Pb/204Pb = 38.3, 87Sr/86Sr = 0.70353 and 143Nd/144Nd = 0.51285. This composition overlaps the central and north Patagonian intraplate basalts in Pb-isotopic space but is slightly less enriched in Sr and Nd-isotopes. It is distinctly different from the FOZO like composition of the south Patagonian intraplate basalts and the nearby Juan Fernandéz plume but similar to the South Atlantic N-MORB and MORB from the southern Chile Ridge segment 4 (Sturm et al., 1999, JGR 104) described as DUPAL type. The DUPAL-MORB type isotopic composition and the plume-like trace element patterns of the Río Colorado lavas suggest the presence of a weak plume beneath the area. The eruption of the large Payún Matrú volcano and the gigantic Pleistocene flood basalts also calls for a thermal anomaly to produce these melts during a weakly compressive tectonic regime with no significant addition of slab fluids. This was supported by Burd et al. (2008, Abstr., 7th Int. Sym. And. Geo.) who recognized a plume-like conductive structure beneath Payún Matrú volcano on an electrical resistivity profile across the Payún Matrú volcanic field. The many Argentine and Chile Ridge EM1 basalts form part of the global DUPAL-anomaly (Hart, 1984, Nature 309) which suggests a common mode of formation of the enriched mantle sources; most likely anciently subducted components in the underlying upper mantle, either in a larger reservoir or as dispersed bodies of material. From there they can rise as small plumes or be entrained in a convecting MORB source mantle.

Implications of 187Os isotopic heterogeneities in a mantle plume: evidence from Gorgona Island and Curaçao

NASA Astrophysics Data System (ADS)

Walker, Richard J.; Storey, Michael; Kerr, Andrew C.; Tarney, John; Arndt, Nicholas T.

1999-03-01

Recent work has suggested that the mafic-ultramafic volcanism in evidence throughout portions of the Caribbean, Central America, and northern South America, including the islands of Gorgona and Curaçao, was generated as part of a middle-Cretaceous, large igneous province. New Re-Os isochron results for tholeiitic basalts from Gorgona and Curaçao indicate crystallization ages of 89.2 ± 5.2 and 85.6 ± 8.1 Ma, respectively, consistent with reported Ar ages. The Gorgona ultramafic suite shows a large range in initial Os isotopic composition, with γ Os values ranging from -0.5 to +12.4. This large range reflects isotopic heterogeneities in the mantle source similar to those observed for modern ocean island basalts. In contrast to ocean island basalts, however, Os isotopic compositions do not correlate with variations in Nd, Sr, or Pb isotopic compositions, which are within the range of depleted mid-ocean ridge basalts. The processes that produced these rocks evidently resulted in the decoupling of Os isotopes from the Nd, Sr, and Pb isotopic systems. Picrites from Curaçao have very uniform, chondritic initial Os isotopic compositions, with initial γ Os values ranging only from -0.4 to ±1.4. Basalts from Curaçao, however, define an isochron with a 187Os-enriched initial isotopic composition (γ Os = +9.5). In contrast to the 187Os-enriched ultramafic rocks from Gorgona, the enrichment in these basalts could have resulted from lithospheric contamination. If the Gorgona and Curaçao rocks were derived from the same plume, Os results, combined with Sr, Nd, and Pb data indicate a heterogeneous plume, with multiple compositionally and isotopically distinct domains. The Os isotopic results require derivation of Os from a minimum of two distinct reservoirs, one with a composition very similar to the chondritic average and one with long-term enriched Re/Os. Oceanic crustal recycling has been invoked to explain most of the 187Os enrichments that have been observed in ocean island basalt sources and could potentially apply to the Gorgona suite. Crustal recycling, however, requires large proportions of very ancient recycled basaltic crust in the sources of the 187Os-enriched ultramafic rocks to explain the magnitude of 187Os enrichments observed. For example, addition of 20% oceanic crust to fertile mantle, and nearly 3 billion years are necessary to generate a reservoir with the Os isotopic composition of the most radiogenic komatiites. If the recycled oceanic crust was added to basalt-depleted mantle, as may be indicated by ɛ Nd values for the komatiites averaging about +10, even larger proportions of older crust are required. Large proportions of oceanic mafic crust in the sources of the 187Os-enriched komatiites, although petrologically conceivable under certain melting conditions, is unlikely here given the limited trace element and lithophile isotope system variations. These results raise questions about the efficacy of using Os isotopes to constrain the proportion of recycled oceanic crust in other plumes. Other possible mechanisms for generating 187Os-enriched mantle include invoking the existence of a 187Os-enriched lower mantle, and minor outer core-lower mantle interactions.

Electrical conductivity of the oceanic asthenosphere and its interpretation based on laboratory measurements

NASA Astrophysics Data System (ADS)

Katsura, Tomoo; Baba, Kiyoshi; Yoshino, Takashi; Kogiso, Tetsu

2017-10-01

We review the currently available results of laboratory experiments, geochemistry and MT observations and attempt to explain the conductivity structures in the oceanic asthenosphere by constructing mineral-physics models for the depleted mid-oceanic ridge basalt (MORB) mantle (DMM) and volatile-enriched plume mantle (EM) along the normal and plume geotherms. The hopping and ionic conductivity of olivine has a large temperature dependence, whereas the proton conductivity has a smaller dependence. The contribution of proton conduction is small in DMM. Melt conductivity is enhanced by the H2O and CO2 components. The effects of incipient melts with high volatile components on bulk conductivity are significant. The low solidus temperatures of the hydrous carbonated peridotite produce incipient melts in the asthenosphere, which strongly increase conductivity around 100 km depth under older plates. DMM has a conductivity of 10- 1.2 - 1.5 S/m at 100-300 km depth, regardless of the plate age. Plume mantle should have much higher conductivity than normal mantle, due to its high volatile content and high temperatures. The MT observations of the oceanic asthenosphere show a relatively uniform conductivity at 200-300 km depth, consistent with the mineral-physics model. On the other hand, the MT observations show large lateral variations in shallow parts of the asthenosphere despite similar tectonic settings and close locations. Such variations are difficult to explain with the mineral-physics model. High conductivity layers (HCL), which are associated with anisotropy in the direction of the plate motion, have only been observed in the asthenosphere under infant or young plates, but they are not ubiquitous in the oceanic asthenosphere. Although the general features of HCL imply their high-temperature melting origin, the mineral-physics model cannot explain them quantitatively. Much lower conductivity under hotspots, compared with the model plume-mantle conductivity suggests the extraction of volatiles from the plume mantle by the ocean island basalt (OIB) magmatism.

Osmium isotopes suggest fast and efficient mixing in the oceanic upper mantle.

NASA Astrophysics Data System (ADS)

Bizimis, Michael; Salters, Vincent

2010-05-01

The depleted upper mantle (DUM; the source of MORB) is thought to represent the complementary reservoir of continental crust extraction. Previous studies have calculated the "average" DUM composition based on the geochemistry of MORB. However the Nd isotope compositions of abyssal peridotites have been shown to extend to more depleted compositions than associated MORB. While this argues for the presence of both relatively depleted and enriched material within the upper mantle, the extent of compositional variability, length scales of heterogeneity and timescales of mixing in the upper mantle are not well constrained. Model calculations show that 2Ga is a reasonable mean age of depletion for DUM while Hf - Nd isotopes show the persistence of a depleted terrestrial reservoir by the early Archean (3.5-3.8Ga). U/Pb zircon ages of crustal rocks show three distinct peaks at 1.2, 1.9, and 2.7Ga and these are thought to represent the ages of three major crustal growth events. A fundamental question therefore is whether the present day upper mantle retains a memory of multiple ancient depletion events, or has been effectively homogenized. This has important implications for the nature of convection and time scales of survival of heterogeneities in the upper mantle. Here we compare published Os isotope data from abyssal peridotites and ophiolitic Os-Ir alloys with new data from Hawaiian spinel peridotite xenoliths. The Re-Os isotope system has been shown to yield useful depletion age information in peridotites, so we use it here to investigate the distribution of Re-depletion ages (TRD) in these mantle samples as a proxy for the variability of DUM. The probability density functions (PDF) of TRD from osmiridiums, abyssal and Hawaiian peridotites are all remarkably similar and show a distinct peak at 1.2-1.3 Ga (errors for TRD are set at 0.2Ga to suppress statistically spurious age peaks). The Hawaiian peridotites further show a distinct peak at 1.9-2Ga, but no oceanic mantle samples with TRD older than 2Ga have been reported. The TRD age peaks overlap with two major crustal building events recorded in the U/Pb crustal zircon ages. Therefore, peridotites from the convecting upper mantle can retain some memory of ancient depletion events, and these depletions are perhaps linked to major crustal building or large-scale mantle melting events. In the case of the Hawaiian peridotites, an ancient depletion event is further supported by some extremely radiogenic Hf isotope compositions. However, the vast majority of oceanic mantle samples show a narrow rage of Os isotope compositions (187Os/188Os = 0.123-0.126) with TRDs at 300-600 Ma. If the upper mantle has been produced continuously (or episodically) since at least the early Archean, it is then surprising that almost all oceanic mantle samples record such young depletion ages. We suggest that convective mixing in the mantle is rigorous enough that effectively re-homogenizes and resets the Os isotope composition of previously depleted peridotites within short time scales (<500Ma). Similarly recent ages have been derived from modeling the Sr, Nd, Hf, Pb isotopic composition of MORBs. This resetting and homogenization can be due to re-equilibration of depleted mantle with enriched components, e.g. recycled basaltic crust or more fertile mantle. Ancient depletion events are only effectively preserved in the sublithospheric mantle samples (e.g. Kaapval, Slave, Wyoming cratons) because they remain isolated from the convective mantle.

Evolving Mantle Sources in Postcollisional Early Permian-Triassic Magmatic Rocks in the Heart of Tianshan Orogen (Western China)

NASA Astrophysics Data System (ADS)

Tang, Gong-Jian; Cawood, Peter A.; Wyman, Derek A.; Wang, Qiang; Zhao, Zhen-Hua

2017-11-01

Magmatism postdating the initiation of continental collision provides insight into the late stage evolution of orogenic belts including the composition of the contemporaneous underlying subcontinental mantle. The Awulale Mountains, in the heart of the Tianshan Orogen, display three types of postcollisional mafic magmatic rocks. (1) A medium to high K calc-alkaline mafic volcanic suite (˜280 Ma), which display low La/Yb ratios (2.2-11.8) and a wide range of ɛNd(t) values from +1.9 to +7.4. This suite of rocks was derived from melting of depleted metasomatized asthenospheric mantle followed by upper crustal contamination. (2) Mafic shoshonitic basalts (˜272 Ma), characterized by high La/Yb ratios (14.4-20.5) and more enriched isotope compositions (ɛNd(t) = +0.2 - +0.8). These rocks are considered to have been generated by melting of lithospheric mantle enriched by melts from the Tarim continental crust that was subducted beneath the Tianshan during final collisional suturing. (3) Mafic dikes (˜240 Ma), with geochemical and isotope compositions similiar to the ˜280 Ma basaltic rocks. This succession of postcollision mafic rock types suggests there were two stages of magma generation involving the sampling of different mantle sources. The first stage, which occurred in the early Permian, involved a shift from depleted asthenospheric sources to enriched lithospheric mantle. It was most likely triggered by the subduction of Tarim continental crust and thickening of the Tianshan lithospheric mantle. During the second stage, in the middle Triassic, there was a reversion to more asthenospheric sources, related to postcollision lithospheric thinning.

Mantle transition zone input to kimberlite magmatism near a subduction zone: Origin of anomalous Nd-Hf isotope systematics at Lac de Gras, Canada

NASA Astrophysics Data System (ADS)

Tappe, Sebastian; Graham Pearson, D.; Kjarsgaard, Bruce A.; Nowell, Geoff; Dowall, David

2013-06-01

Late Cretaceous-Eocene kimberlites from the Lac de Gras area, central Slave craton, show the most extreme Nd-Hf isotope decoupling observed for kimberlites worldwide. They are characterized by a narrow range of moderately enriched Nd isotope compositions (ɛNd(i)=-0.4 to -3.5) that contrasts strongly with their moderately depleted to highly enriched ɛHf(i) values (+3.9 to -9.9). Although digestion of cratonic mantle material in proto-kimberlite melt can theoretically produce steep arrays in Nd-Hf isotope space, the amount of contaminant required to explain the Lac de Gras data is unrealistic. Instead, it is more plausible that mixing of compositionally discrete melt components within an isotopically variable source region is responsible for the steep Nd-Hf isotope array. As development of strongly negative ΔɛHf requires isotopic aging of a precursor material with Sm/Nd≫Lu/Hf for billion-year timescales, a number of models have been proposed where ancient MORB crust trapped in the mantle transition zone is the ultimate source of the extreme Hf isotope signature. However, we provide a conceptual modification and demonstrate that OIB-type domains within ancient subducted oceanic lithosphere can produce much stronger negative ΔɛHf during long-term isolation. Provided that these OIB-type domains have lower melting points compared with associated MORB crust, they are among the first material to melt within the transition zone during thermal perturbations. The resulting hydrous alkali silicate melts react strongly with depleted peridotite at the top of the transition zone and transfer negative ΔɛHf signatures to less dense materials, which can be more easily entrained within upward flowing mantle. Once these entrained refertilized domains rise above 300 km depth, they may become involved in CO2- and H2O-fluxed redox melting of upper mantle peridotite beneath a thick cratonic lid. We argue that incorporation of ancient transition zone material, which includes ultradeep diamonds, into the convecting upper mantle source region of Lac de Gras kimberlites was due to vigorous mantle return flow. This occurred in direct response to fast and complex subduction along the western margin of North America during the Late Cretaceous.

Cenozoic mantle composition evolution of southern Tibet indicated by Paleocene ( 64 Ma) pseudoleucite phonolitic rocks in central Lhasa terrane

NASA Astrophysics Data System (ADS)

Qi, Yue; Gou, Guo-Ning; Wang, Qiang; Wyman, Derek A.; Jiang, Zi-Qi; Li, Qiu-Li; Zhang, Le

2018-03-01

The question of whether continental subduction processes in collisional orogenic belts can trigger wide-spread mantle metesomatism and crustal material recycling remains unresolved. Miocene (25-8 Ma) ultrapotassic rocks in southern Tibet are the only mantle-derived magmatic rocks emplaced after the collision between India and Asia and they have been linked to the onset of east-west extensional stresses as the surface uplift of the Tibetan Plateau reached near-maximum elevation. However, their petrogenesis remains highly controversial, particularly the issue of whether their extremely enriched Sr-Nd isotopic characteristics were related to metasomatism derived from subducted Indian continental materials during the Cenozoic. Here we report on a Paleocene silicate-unsaturated, pseudoleucite phonolitic dike, in the Rongniduo area of central Lhasa terrane. In-situ SIMS (secondary ion mass spectrometry) apatite U-Pb age indicates the dike was generated at 64.1 ± 4.2 Ma, which slightly predates the age of initial India and Asia collision (about 55-50 Ma). This is the oldest age yet reported for ultrapotassic rocks in southern Tibet. Samples from this dike have distinctly more depleted Sr-Nd (whole rock: (87Sr/86Sr)i = 0.7064 to 0.7062, εNd(t) = - 1.5 to 0.4; in situ apitite: (87Sr/86Sr)i = 0.7059 to 0.7060, εNd(t) = - 2.0 to 0.4) isotopic compositions, than those of Miocene (25-8 Ma) ultrapotassic rocks in the central Lhasa terrane ((87Sr/86Sr)i = 0.7106 to 0.7399, εNd(t) = - 10.6 to - 18.5). Our new data provides important constraints on pre-collisional mantle characteristics beneath the Lhasa terrane. We suggest that these 64 Ma pseudoleucite phonolitic rocks were derived from the enriched lithospheric mantle metasomatized by subducted Tethyan oceanic materials in response to Neo-Tethyan slab roll-back. As a consequence, the younger Miocene ultrapotassic rocks, which display different geochemical compositions from the pre-collisional ultrapotassic rocks, were most probably derived from a mantle source metasomatized by subducted Indian continental materials after 64 Ma. Our results indicate that the addition of subducted continental components plays an important role in changing mantle constituents beneath collisional orogenic belts.

Geochemistry of the Seamounts at the Southeast Chatham Rise, New Zealand

NASA Astrophysics Data System (ADS)

Jolis, E. M.; Hoernle, K.; Hauff, F.; Garbe-Schönberg, D.; Werner, R.; Gohl, K.

2017-12-01

The submarine Chatham Rise, east Zealandia, is a key location of the early continental breakup of the eastern Gondwana (< 100 Ma; [1]). It has been suggested that a mantle plume beneath Zealandia and West Antarctica existed and that a slab window formed as a consequence of the collision of the Hikurangi oceanic plateau with the Chatham Rise, allowing deeper mantle material to upwell and hence cause the rifting. However, the exact processes that have led to this rifting and the sequence of reorganization in the upper mantle in course of and after the breakup of Zealandia from West Antarctica are still unclear. We present new major and trace element and Sr-Nd and high-precision Pb isotope data from submarine samples recovered during the R/V Sonne research expedition SO246 at the southeast Chatham Rise, covering the Chatham Rise Terrace and adjacent areas of the margin and the abyssal plain. The samples include alkali and tholeiitic basalts and minor basanite and trachybasalt, all of which have a composition between ocean island basalt (OIB) and mid-ocean-ridge basalt (MORB). Trace element ratios (e.g., Th/Yb, Nb/Yb) indicate that all but one seamount were derived from enriched sources at a low degree of melting, while one of the seamounts close to the abyssal plain was derived from a depleted mantle source at a high degree of melting. Sr-Nd-Pb isotope variations further support contribution of at least three distinct mantle source components, including a HIMU (high time-integrated U/Pb)-type sources, an enriched mantle (EM)-type sources, and a depleted mantle (N-MORB)-type source. These observations appear to be consistent with previous published data and models proposed by [2] and [3]. These sources will be placed in a chronological framework by incorporating further geochemical data and 40Ar-39Ar ages, providing us better insights into the sequence of events and magmatic processes that occurred at this region. References:[1] Davy et al. (2008), Hikurangi Plateau: Crustal structure, rifted formation, and Gondwana subduction history, G3, 9, Q07004. [2] Hoernle et al. (2006), Cenozoic intraplate volcanism on New Zealand: Upwelling induced by lithospheric removal, EPSL, 248, 350-367. [3] Timm et al. (2010), Temporal and geochemical evolution of the Cenozoic intraplate volcanism of Zealandia, Earth-Sci. Rev., 98, 38-64.

Redox Heterogenity in MORB

NASA Astrophysics Data System (ADS)

Cottrell, E.; Kelley, K. A.

2012-12-01

Mantle oxygen fugacity (fO2) has a first-order effect on the petrogenesis of mantle-derived melts and the speciation of mantle fluids. Current debate centers on the spatial uniformity of upper mantle fO2 and its constancy through geologic time. We use iron K-edge X-ray absorption near-edge structure (μXANES) spectroscopy to provide Fe3+ /ΣFe ratios of submarine mantle-derived basalts from mid-ocean ridges (MORB) as a proxy for fO2. A global survey of primitive (>8.75 wt% MgO) MORB glasses at spreading centers, unaffected by plumes, reveals a decrease in Fe3+ /ΣFe ratio of 12% relative with indices of mantle enrichment such as 87/86Sr, 208/204Pb, Ba/La, and Rb/Sr ratios. The strong negative correlation between upper mantle fO2 and enrichment recorded by MORB glasses contrasts with the positive relationship hinted at by abyssal peridotite oxybarometry (e.g. Ballhaus, CMP, 1993) and the general prediction of a positive correlation born of the expectation that Fe3+ can be treated as more incompatible than Fe2+ during mantle melting. These data unequivocally link upper mantle oxidation state to mantle source enrichment. EMORB generation is commonly attributed to subduction-related processes. That EMORB is more reduced than NMORB implies that deeply subducted and recycled lithologies, such as anoxic sediment, may be more reduced than ambient mantle. Negative correlations between traditional tracers of recycled sediment (e.g. +Nb anomaly, high 87/86Sr, high LILE/LREE) and redox support this hypothesis. Preservation of redox signatures on plate-recycling timescales of hundreds of millions to billions of years would require the mantle to be very poorly buffered. Alternatively, MORB Fe3+ /ΣFe ratios may be generated in situ beneath ridges as a function of variable carbon content. The shallow MORB source is too oxidized to stabilize graphite (Cottrell and Kelley, EPSL, 2011) and carbon exists as oxides. Decreasing fO2 with increasing depth eventually stabilizes reduced carbon species (diamond, carbides, alloys), however, and aCO2 may buffer mantle assemblages. Upon ascent, reduced carbon in upwelling mantle must oxidize, reducing Fe in the process such that more carbon-rich mantle would arrive at the surface with a lower Fe3+ /ΣFe ratio. We cannot directly correlate Fe3+ /ΣFe ratios with CO2 concentrations because submarine basalts have variably degassed CO2; however, the unequivocally carbon-rich sample 2πD43 (popping rock) does record a low Fe3+ /ΣFe ratio. CO2 variations on the order of 80 ppm in the mantle source would explain the range of MORB/EMORB Fe3+ /ΣFe ratios we observe, indicating a possible range of carbon concentrations in subduction-related lithologies. The relationships between MORB Fe3+ /ΣFe ratios, trace elements, and isotopes are consistent with modeled mixtures of depleted melts and low-degree carbonatitic melts of ancient subducted igneous crust plus 5-15% sediment (Stracke et al., G3, 2001) using the near-solidus carbonatitic partition coefficients of Dasgupta et al., Chem Geol, (2009). It may be that low degree carbonatitic melts even act through geologic time to scavenge and fractionate trace elements, creating enriched high-carbon reservoirs. Low Fe3+ /ΣFe ratios, and even EMORB itself, may therefore herald greater carbon concentrations, and the influence of low-degree carbonatitic melts, in Earth's mantle.

Evaluating Crustal Contamination Effects on the Lithophile Trace Element Budget of Shergottites

NASA Technical Reports Server (NTRS)

Brandon, A. D.; Ferdous, J.; Peslier, A. H.

2017-01-01

The origin of the incompatible trace element (ITE) enriched compositions of shergottites has been a point of contention for decades [1-2]. Two scenarios have been proposed, the first is that enriched shergottite compositions reflect an ITE-enriched mantle source, whereas in the second, the ITE enrichment reflects crustal contamination of mantle-derived parent magmas. Evidence supporting the first scenario is that the ITE-enriched shergottite compositions are consistent with the outcomes of magma ocean crystallization [3], and that Os-Nd isotope relationships for shergottites cannot be explained by realistic crustal contamination models [4]. In contrast, Cl and S isotopes are consistent with shergottite magmas interacting with Mars crust [5,6], and ITE-enriched olivine-hosted melt inclusions and interstitial glass are found in depleted shergottite Yamato 980459 [7]. These findings indicate that some level of crustal interaction occurred but the question of whether ITE-enrichments in some bulk shergottites reflect crustal contamination remains open. Recently, a Mars crustal breccia meteorite has been found, NWA 7034 and its paired stones, that is our best analogue to an average of Mars ancient crust [8-10]. This allows for better constraints on crustal contamination of shergottite magmas. We modeled magma-crust mixing and assimilation-fractional crystallization (AFC) using ITE-depleted shergottite compositions and bulk NWA 7034 and its clasts as end-members. The results of these models indicate that crustal contamination can only explain the ITE-enriched compositions of some bulk shergottites under unusual circumstances. It is thus likely that the shergottite range of compositions reflects primarily mantle sources.

The peculiar geochemical signatures of São Miguel (Azores) lavas: Metasomatised or recycled mantle sources?

NASA Astrophysics Data System (ADS)

Beier, Christoph; Stracke, Andreas; Haase, Karsten M.

2007-07-01

The island of São Miguel, Azores consists of four large volcanic systems that exhibit a large systematic intra-island Sr-Nd-Pb-Hf isotope and trace element variability. The westernmost Sete Cidades volcano has moderately enriched Sr-Nd-Pb-Hf isotope ratios. In contrast, lavas from the easternmost Nordeste volcano have unusually high Sr and Pb and low Nd and Hf isotope ratios suggesting a long-term evolution with high Rb/Sr, U/Pb, Th/Pb, Th/U and low Sm/Nd and Lu/Hf parent-daughter ratios. They have trace element concentrations similar to those of the HIMU islands, with the exception of notably higher alkali element (Cs, Rb, K, Ba) and Th concentrations. The time-integrated parent-daughter element evolution of both the Sete Cidades and Nordeste source matches the incompatibility sequence commonly observed during mantle melting and consequently suggests that the mantle source enrichment is caused by a basaltic melt, either as a metasomatic agent or as recycled oceanic crust. Our calculations show that a metasomatic model involving a small degree basaltic melt is able to explain the isotopic enrichment but, invariably, produces far too enriched trace element signatures. We therefore favour a simple recycling model. The trace element and isotopic signatures of the Sete Cidades lavas are consistent with the presence of ancient recycled oceanic crust that has experienced some Pb loss during sub-arc alteration. The coherent correlation of the parent-daughter ratios (e.g. Rb/Sr, Th/U, U/Pb) and incompatible element ratios (e.g. Nb/Zr, Ba/Rb, La/Nb) with the isotope ratios in lavas from the entire island suggest that the Sete Cidades and Nordeste source share a similar genetic origin. The more enriched trace element and isotopic variations of Nordeste can be reproduced by recycled oceanic crust in the Nordeste source that contains small amounts of evolved lavas (˜ 1-2%), possibly from a subducted seamount. The rare occurrence of enriched source signatures comparable to Nordeste may be taken as circumstantial evidence that stirring processes in the Earth's mantle are not able to homogenise material within the size of seamounts over timescales of mantle recycling.

Chemical stratification of cratonic lithosphere: constraints from the Northern Slave craton, Canada

NASA Astrophysics Data System (ADS)

Kopylova, Maya G.; Russell, James K.

2000-08-01

We describe the mineralogical and chemical composition of the Northern Slave mantle as deduced from xenoliths of peridotite within the Jericho kimberlite, Northwest Territories. Our data set includes modal, major, trace and rare earth element compositions of bulk samples of spinel peridotite, low-T and high-T garnet peridotite and minor pyroxenite. Compared to primitive upper mantle, Jericho peridotite shows depletion in the major elements and enrichment in incompatible elements (except for HREE). The Slave mantle is also uniquely stratified. Older, depleted spinel peridotite extends to a depth of 80-100 km and is underlain by garnet peridotite which shows a gradual decrease in Mg# with depth to 200 km. The youngest layer of fertile garnet peridotite, enriched in clinopyroxene and garnet, is underlain by a pyroxenite-rich horizon at the base of the petrological lithosphere. The Northern Slave is further distinguished from the Kaapvaal and Siberian upper mantle by a marked vertical stratification in Mg#, lower abundances of orthopyroxene and higher abundances of clinopyroxene. In addition, a deeper layer of garnet peridotite below Jericho shows less depletion than low-T peridotite from other cratons. The Northern Slave peridotite results from a series of chemical events that include: (i) high-degree melting of pyrolite at P>3 Gpa for low-T peridotite and lower pressure melting for high-T peridotite, (ii) enrichment of low-T spinel peridotite in orthopyroxene, and (iii) pervasive metasomatic enrichment in alkali and LREE's by kimberlite-related fluids. The chemical stratification described for two of the three lithospheric domains of the Slave craton makes this craton an exception among cratons with commonly unstratified lithospheres. The gradual increase in fertility with depth below the Slave craton is related to age stratification and may have formed by incremental downward growth of mantle lithosphere with time, and/or later re-fertilization of deeper mantle horizons.

Small scale inhomogeneity in the mantle source of the Cape Verde hotspot is probably related to plume complexity: implications from Sr, Nd and high precision Pb isotopes and geochemistry

NASA Astrophysics Data System (ADS)

Holm, P. M.; Sørensen, R. V.

2009-04-01

The volcanic rocks of one of the major islands of the Cape Verde hotspot have been investigated in order to test mantle plume models. From the centre of the Cape Verde Rise an array of islands trend west, the northern HIMU-type Cape Verde Islands. Of these, São Nicolau (SN) is the easternmost and Santo Antão the westernmost. Sixty samples of primitive (MgO = 9-14 wt%) basanitic composition from SN that represent the four volcanic stages of the 9 - 0.1 Ma evolution of the island have been analysed for Sr, Nd and high precision Pb isotopic composition. Pb ranges to a less radiogenic composition than on SA [1] and has lower 8/4 than the rocks of the southern EM1-type Cape Verde islands. Most SN lavas have a young HIMU character with negative 7/4. The most radiogenic Pb at SN is less thorogenic than Pb at SA. Temporal variation is also evident: An intermediate age group of samples have particularly low La/Nb = 0.4 - 0.5 and the least LREE-enrichment for SN. The youngest group of rocks has the lowest Zr/Nb = 2.5 - 3.0 and the most unradiogenic Sr and radiogenic Nd in the archipelago. At least four of the mantle source components for the SN magmas are different from any found in the SA magmas. High precision Pb data allow identification of parallel trends for northern SN and the southern island Santiago, which therefore must have unrelated source components. For the northern Cape Verde islands source compositions vary from E to W as well as with time. This cannot be explained by stationary enriched lithosphere components. The derivation of melts from a complex plume source is modelled. [1] Holm P.M., Wilson J.R., Christensen B.P., Hansen S.L., Hein K.M., Mortensen A.K., Pedersen R., Plesner S., and Runge M.K. (2006) JPetrol 47, 145-189.

What Factors Control Platinum-Group Element (PGE) Abundances in Basalts From the Ontong Java Plateau?

NASA Astrophysics Data System (ADS)

Chazey, W. J.; Neal, C. R.

2002-12-01

Eleven samples encompassing four sites drilled by Ocean Drilling Program Leg 192 to the Ontong Java Plateau (OJP) were analyzed for major, trace and platinum-group (PGEs: Ir, Ru, Rh, Pt, and Pd) elements. Based on major and trace element chemistry, these are divided into two groups: a primitive group, which was newly discovered on Leg 192, and Kwaimbaita-type basalts, which are ubiquitous on the OJP (cf. Tejada et al., 2002, J. Pet. 43:449). The primitive group is relatively enriched in MgO, Ni, and Cr and relatively depleted in incompatible elements compared to the Kwaimbaita-type basalts. Petrography indicates that the fractionating phases during emplacement of both types of basalts were olivine and Cr-spinel +/- plagioclase +/- cpx. Normalized PGE profiles are fractionated, but exhibit a flattening between Ru and Ir and occasionally an enrichment in Ir. It has been shown that chromite can preferentially incorporate Os and Ru (Kd ?150) over Ir (Kd ?100), which may account for the Ir and Ru systematics. We do not consider sulfide to be a factor in fractionating the PGEs because it is either absent or present as a trace phase in these basalts and the OJP basalts are sulfur undersaturated (Michael and Cornell, 1996, EOS 77:714). Additionally, the primitive samples from the OJP also have Cu/Pd ratios (4500-8000) that are roughly similar to primitive mantle (7300), and have a generally flat transition from Pd to Y on a primitive mantle-normalized plot. It is unlikely that these samples reached sulfur saturation. The Kwaimbaita-type basalts have slightly elevated Cu/Pd ratios (9000-14000). While there are subtle differences between the PGE profiles of basalts from the Leg 192 drill cores compared to OJP basalts from subaerial outcrops in the Solomon Islands (e.g., the former have general lower Pt/Rh and higher Rh/Ru ratios), it is apparent that silicate and oxide phases are controlling the PGE profiles and abundances. For example, the six samples analyzed from Site 1185 demonstrate a positive correlation of Ru and Ir with Cr and Ni, suggesting a close association of these elements with the observed olivine and Cr-spinel phenocrysts. For all OJP basalts for which we have PGE data, there is a general positive correlation using MgO (or Cr or Ni) as a fractionation index and PGE abundance as well as ratios such as Pt/Y. Therefore, fractional crystallization controls the PGE contents of the OJP basalts. However, as noted by Ely and Neal (2002, Chem. Geol., in press) the abundances require a source enriched in the PGEs over upper mantle and, in some cases, primitive mantle. Such sources require a PGE enriched component that could be from the outer core, although as noted by Parkinson et al. (2001, EOS 82:F1398) this component is not always required. Further work is underway to substantiate this.

Geochronological, geochemical, and Sr-Nd-Hf isotopic characteristics of Cretaceous monzonitic plutons in western Zhejiang Province, Southeast China: New insights into the petrogenesis of intermediate rocks

NASA Astrophysics Data System (ADS)

Liu, Liang; Qiu, Jian-Sheng; Zhao, Jiao-Long; Yang, Ze-Li

2014-05-01

We present comprehensive petrological, geochemical, and Sr-Nd-Hf isotopic data for the Matou and Dalai plutons in western Zhejiang Province, Southeast China, with the aim of constraining the petrogenesis of monzonites and to offer new insights into the deep processes of interaction between crustal- and mantle-derived magmas beneath SE China. The Matou pluton comprises quartz monzonite, whereas the Dalai pluton consists of quartz monzodiorite. Zircon U-Pb ages obtained by laser ablation-inductively coupled plasma-mass spectrometry show that both plutons were emplaced at 99-101 Ma. Rocks of both plutons are intermediate to silicic, metaluminous to weakly peraluminous, subalkaline, and K-rich in composition. Samples of the plutons are enriched in large ion lithophile (e.g., Rb, K, and Pb) and light rare earth elements, depleted in high-field strength elements (e.g., Nb, Ta, and Ti), and have small negative or no Eu anomalies. In addition, the rocks have high Mg# values (up to 53.9), high zircon ɛHf(t) values (up to - 1.4), and low Nb/U and Ta/U ratios. Geochemical evidence suggests that both depleted asthenospheric and metasomatically enriched mantle components were involved in the formation of these monzonitic rocks. The presence of inherited zircons with Palaeoproterozoic ages and zircons with unusually low ɛHf(t) values (- 12.9) in the Matou quartz monzonites indicates that ancient crustal materials were also involved in their petrogenesis. In combination with the presence of abundant mafic microgranular enclaves (MMEs) with spheroidal to ellipsoidal-ovoidal shapes and xenocrysts within the more diffused enclaves, and the results of trace element modelling, we suggest that the Matou quartz monzonites were generated by mixing between mantle-derived mafic magmas and crustally derived silicic magmas. The Dalai pluton is relatively homogeneous and contains fewer MMEs than the Matou pluton. Zircons from the Dalai pluton show no inherited components, indicating that crustal materials have played a limited role in the petrogenesis of the quartz monzodiorites. The Dalai quartz monzodiorites have lower SiO2 contents, higher Mg# values, and considerably higher and variable Cr, Co, and Ni concentrations than the Matou quartz monzonites. Zircon Hf isotopic compositions of the Dalai pluton are relatively homogeneous (ɛHf(t) = - 5.2 to - 3.2). The combined petrological, geochemical, and isotopic features indicate that the Dalai monzodiorites were generated by olivine- and pyroxene-dominated fractional crystallisation from basaltic magmas, which were in turn produced by mixing between melts from depleted asthenosphere and subduction-enriched mantle. Our interpretation implies that Late Mesozoic monzonitic rocks in Southeast China require a significant input of mantle melts, and some may have been generated solely by fractionation of basaltic magmas. This petrogenetic model may be applicable to other monzonitic rocks in Southeast China, and to similar tectonic settings and sites of monzonitic magma generation worldwide.

Water content in the SW USA mantle lithosphere: FTIR analysis of Dish Hill and Kilbourne Hole pyroxenites

NASA Astrophysics Data System (ADS)

Gibler, R.; Peslier, A. H.; Schaffer, L. A.; Brandon, A. D.

2014-12-01

Kilbourne Hole (NM, USA) and Dish Hill (CA, USA) mantle xenoliths sample continental mantle in two different tectonic settings. Kilbourne Hole (KH) is located in the Rio Grande rift. Dish Hill (DH) is located in the southern Mojave province, an area potentially affected by subduction of the Farallon plate beneath North America [1]. FTIR analyses were obtained on well characterized pyroxenite, dunite and wehrlite xenoliths, thought to represent crystallized melts at mantle depths. PUM normalized REE patterns of the KH bulk-rocks are slightly LREE enriched and consistent with those of liquids generated by < 5% melting of a spinel peridotite source [2]. Clinopyroxenes contain from 272 to 313 ppm weight H2O similar to the lower limit of KH peridotite clinopyroxenes (250-530 ppm H2O, [3]). This is unexpected as crystallized melts like pyroxenites should concentrate water more than residual mantle-like peridotites, given that H is incompatible. PUM normalized bulk REE of the DH pyroxenites are characterized by flat to LREE depleted REE profiles consistent with > 6% melting of a spinel peridotite source. Pyroxenite pyroxenes have no detectable water but one DH wehrlite, which bulk-rock is LREE enriched, has 4 ppm H2O in orthopyroxene and <1ppm in clinopyroxene. The DH pyroxenites may thus come from a dry mantle source, potentially unaffected by the subduction of the Farallon plate. These water-poor melts either originated from shallow oceanic lithosphere overlaying the Farallon slab [4] or from continental mantle formed > 2 Ga [5]. The Farallon subduction appears to have enriched in water the southwestern United States lithospheric mantle further east than DH, beneath the Colorado plateau [6]. [1] Atwater, 1970 Tectonophysics 31, 145-165. [2] Shaw, 2000 CM 38, 1041-1064. [3] Schaffer et al, 2013 AGU Fall Meeting. [4] Luffi et al, 2009 JGR 114, 1-36. [5] Armytage et al, 2013 GCA 137, 113-133. [6] Li et al, 2008 JGR 113, 1-22.

Tracing the HIMU component within Pan-African lithosphere beneath northeast Africa: Evidence from Late Cretaceous Natash alkaline volcanics, Egypt

NASA Astrophysics Data System (ADS)

Abu El-Rus, M. A.; Chazot, G.; Vannucci, R.; Paquette, J.-L.

2018-02-01

A large late Cretaceous ( 90 Ma) volcanic field (the Natash volcanic province) crops out in southeast Egypt at the northwestern boundary of the Arabian-Nubian shield. The lavas are mainly of alkaline affinity and exhibit a continuous compositional range from alkali olivine basalt (AOB) to trachyte and rhyolite. All basaltic lavas in the province record various extents of fractional crystallization of olivine, clinopyroxene, plagioclase and spinel. The basaltic lavas show variations in Sr-Nd-Pb-Hf isotopic ratios [(87Sr/86Sr)i = 0.7030-0.70286; (143Nd/144Nd)i = 0.512653-0.512761; (206Pb/204Pb)i = 19.28-19.94; (177Hf-176Hf)i = 0.28274-0.28285], that correlate markedly with the major and trace element ratios and abundances. Assimilation of crustal material cannot explain these correlations, and we invoke instead melting of a multicomponent mantle source. We infer the existence of High-μ (HIMU), Enriched mantle type-I (EM-I) and Depleted mantle (DM) domains in the melting source, with a predominant contribution from the HIMU-type. We suggests further that the basaltic lavas originate from low degrees of partial melting (F < 5%) at moderate potential temperatures (TP) 1391-1425 °C and pressures of 2.0-2.6 GPa. The melting pressure estimations imply that melting entirely occurred within lithospheric mantle, most likely in the presence of residual amphibole as presence negative K-anomalies in the primitive mantle-normalized patterns of the fractionation-corrected melts. The presence of amphibole within the lithosphere is a strong evidence that the lithospheric mantle underwent metasomatic enrichment prior to melting in Late Cretaceous. This metasomatic event affected on the Pb isotopic compositions of the Natash volcanics by adding Th and U to the melting source. Time-integrated calculations to remove the decoupling between 206Pb and 207Pb isotopes that most probably resulted from the metasomatic event indicate a tentative link between the metasomatism occurring in the Pan-African lithospheric mantle and the formation of juvenile crust during the Pan-African Orogeny. A two stage evolution model is therefore proposed for volcanism in the Natash area: fluxing of the lithosphere by hydrous fluids during Pan-African Orogeny forming a hybrid lithospheric mantle that in Late Cretaceous underwent thermal erosion and melting in response to upwelling asthenosphere, possibly at the onset of the extensional fracturing preceded the doming of the Afro-Arabian Shield.

Meter-scale Hf isotopic changes in the MORB mantle by interaction with pyroxenite-derived melts: insight from the Ligurian Ophiolites (Italy)

NASA Astrophysics Data System (ADS)

Rampone, E.; Borghini, G.; Class, C.; Goldstein, S. L.; Cai, Y.; Cipriani, A.; Zanetti, A.; Hofmann, A. W.

2017-12-01

Melt percolation and melt-peridotite interaction are efficient processes in creating chemical and isotopic heterogeneity in the upper mantle at variable scale. Such processes can generate a pyroxenite-bearing veined mantle often invoked as source of the oceanic magmatism. Natural examples of such veined mantle are however scarce, as well as studies combining geochemical and isotopic investigations with detailed field control and sampling. Mantle lherzolites in the External Liguride ophiolites (Northern Apennines) contain cm-thick pyroxenite layers that originated by deep infiltration of MORB-type melts (Borghini et al., 2016, J.Petrology 57). In a previous study (Borghini et al, 2013, Geology 41), we showed that geochemical gradients are preserved across the pyroxenite-peridotite contact, and the host peridotites have been modified in terms of modal, chemical and Nd isotopic composition, by reaction with pyroxenite-derived melts. Such interaction caused systematic lowering of the Sm/Nd ratios in clinopyroxene of the host peridotite at >0.1 m scale, and over time this resulted in decimeter-scale Nd isotopic heterogeneity, larger than the Nd isotopic variability of global abyssal peridotites. In this paper, we show the results of Lu-Hf isotopic investigations, performed on the same peridotite-pyroxenite profiles, aimed to test the existence of Hf isotopic changes in mantle peridotite induced by a pyroxenite component. In both peridotites and pyroxenites, initial (160Ma) EpsilonHf versus EpsilonNd values define an overall positive correlation, almost covering the entire MORB variation, and extending beyond the depleted end of the MORB field. As documented for Nd isotopes, the lowest 176Lu/177Hf and 176Hf/177Hf ratios are shown by peridotites adjacent to pyroxenite layers, as a result of reaction with pyroxenite-derived melts. Internal Lu-Hf isochrones on two pyroxenite-peridotite profiles have yielded Ordovician ages of pyroxenite emplacement, consistent with previous Sm-Nd investigations (Borghini et al., 2013). Our results point to predominant coherent behaviour of Hf and Nd isotopes during melt percolation and melt-peridotite interaction, and corroborate the role of such processes in creating the enriched mantle components often invoked to explain the isotopic variability of MORBs.

Oxygen fugacity profile of the oceanic upper mantle and the depth of redox melting beneath ridges

NASA Astrophysics Data System (ADS)

Davis, F. A.; Cottrell, E.

2014-12-01

Oxygen fugacity (fO2) of a mantle mineral assemblage, controlled primarily by Fe redox chemistry, sets the depth of the diamond to carbonated melt reaction (DCO3). Near-surface fO2 recorded by primitive MORB glasses and abyssal peridotites anchor the fO2 profile of the mantle at depth. If the fO2-depth relationship of the mantle is known, then the depth of the DCO3 can be predicted. Alternatively, if the DCO3 can be detected geophysically, then its depth can be used to infer physical and chemical characteristics of upwelling mantle. We present an expanded version of a model of the fO2-depth profile of adiabatically upwelling mantle first presented by Stagno et al. (2013), kindly provided by D. Frost. The model uses a chemical mass balance and empirical fits to experimental data to calculate compositions and modes of mantle minerals at specified P, T, and bulk Fe3+/ƩFe. We added P and T dependences to the partitioning of Al and Ca to better simulate the mineralogical changes in peridotite at depth and included majorite component in garnet to increase the depth range of the model. We calculate fO2 from the mineral assemblages using the grt-ol-opx oxybarometer (Stagno et al., 2013). The onset of carbonated melting occurs at the intersection of a Fe3+/ƩFe isopleth with the DCO3. Upwelling mantle is tied to the DCO3 until all native C is oxidized to form carbonated melts by reduction of Fe3+ to Fe2+. The depth of intersection of a parcel of mantle with the DCO3 is a function of bulk Fe3+/ƩFe, potential temperature, and bulk composition. We predict that fertile mantle (PUM) along a 1400 °C adiabat, with 50 ppm bulk C, and Fe3+/ƩFe = 0.05 after C oxidation begins redox melting at a depth of 250 km. The model contextualizes observations of MORB redox chemistry. Because fertile peridotite is richer in Al2O3, the Fe2O3-bearing components of garnet are diluted leading to lower fO2 at a given depth compared to refractory mantle under the same conditions. This may indicate that the negativecorrelation observed between enrichment and fO2 at ridges (Cottrell and Kelley, 2013) is a consequence of the increased fertility of remixing recycled crust into the mantle. Addition of reduced C to the mantle during subduction can also explain this observation. Geophysical detection of the depth of the DCO3 may resolve these hypotheses.

The oxygen isotope composition of Karoo and Etendeka picrites: High δ18O mantle or crustal contamination?

NASA Astrophysics Data System (ADS)

Harris, Chris; le Roux, Petrus; Cochrane, Ryan; Martin, Laure; Duncan, Andrew R.; Marsh, Julian S.; le Roex, Anton P.; Class, Cornelia

2015-07-01

Oxygen isotope compositions of Karoo and Etendeka large igneous province (LIP) picrites and picrite basalts are presented to constrain the effects of crustal contamination versus mantle source variation. Olivine and orthopyroxene phenocrysts from lavas and dykes (Mg# 64-80) from the Tuli and Mwenezi (Nuanetsi) regions of the ca 180 Ma Karoo LIP have δ18O values that range from 6.0 to 6.7 ‰. They appear to have crystallized from magmas having δ18O values about 1-1.5 ‰ higher than expected in an entirely mantle-derived magma. Olivines from picrite and picrite basalt dykes from the ca 135 Ma Etendeka LIP of Namibia and Karoo-age picrite dykes from Dronning Maud Land, Antarctica, do not have such elevated δ18O values. A range of δ18O values from 4.9 to 6.0 ‰, and good correlations between δ18O value and Sr, Nd and Pb isotope ratios for the Etendeka picrites are consistent with previously proposed models of crustal contamination. Explanations for the high δ18O values in Tuli/Mwenezi picrites are limited to (1) alteration, (2) crustal contamination, and (3) derivation from mantle with an abnormally high δ18O. Previously, a variety of models that range from crustal contamination to derivation from the `enriched' mantle lithosphere have been suggested to explain high concentrations of incompatible elements such as K, and average ɛNd and ɛSr values of -8 and +16 in Mwenezi (Nuanetsi) picrites. However, the primitive character of the magmas (Mg# 73), combined with the lack of correlation between δ18O values and radiogenic isotopic compositions, MgO content, or Mg# is inconsistent with crustal contamination. Thus, an 18O-enriched mantle source having high incompatible trace element concentration and enriched radiogenic isotope composition is indicated. High δ18O values are accompanied by negative Nb and Ta anomalies, consistent with the involvement of the mantle lithosphere, whereas the high δ18O themselves are consistent with an eclogitic source. Magma δ18O values about 1 ‰ higher than expected for mantle-derived magma are also a feature of the Bushveld mafic and ultramafic magmas, and the possibility exists that a long-lived 18O-enriched mantle source has existed beneath southern Africa. A mixed eclogite peridotite source could have developed by emplacement of oceanic lithosphere into the cratonic keel during Archaean subduction.

Differentiation of magma oceans and the thickness of the depleted layer on Venus

NASA Technical Reports Server (NTRS)

Solomatov, V. S.; Stevenson, D. J.

1993-01-01

Various arguments suggest that Venus probably has no asthenosphere, and it is likely that beneath the crust there is a highly depleted and highly viscous mantle layer which was probably formed in the early history of the planet when it was partially or completely molten. Models of crystallization of magma oceans suggest that just after crystallization of a hypothetical magma ocean, the internal structure of Venus consists of a crust up to about 70 km thickness, a depleted layer up to about 500 km, and an enriched lower layer which probably consists of an undepleted 'lower mantle' and heavy enriched accumulates near the core-mantle boundary. Partial or even complete melting of Venus due to large impacts during the formation period eventually results in differentiation. However, the final result of such a differentiation can vary from a completely differentiated mantle to an almost completely preserved homogeneous mantle depending on competition between convection and differentiation: between low viscosity ('liquid') convection and crystal settling at small crystal fractions, or between high viscosity ('solid') convection and percolation at large crystal fractions.

Siderophile element constraints on the origin of the Moon

PubMed Central

Walker, Richard J.

2014-01-01

Discovery of small enrichments in 182W/184W in some Archaean rocks, relative to modern mantle, suggests both exogeneous and endogenous modifications to highly siderophile element (HSE) and moderately siderophile element abundances in the terrestrial mantle. Collectively, these isotopic enrichments suggest the formation of chemically fractionated reservoirs in the terrestrial mantle that survived the putative Moon-forming giant impact, and also provide support for the late accretion hypothesis. The lunar mantle sources of volcanic glasses and basalts were depleted in HSEs relative to the terrestrial mantle by at least a factor of 20. The most likely explanations for the disparity between the Earth and Moon are either that the Moon received a disproportionately lower share of late accreted materials than the Earth, such as may have resulted from stochastic late accretion, or the major phase of late accretion occurred prior to the Moon-forming event, and the putative giant impact led to little drawdown of HSEs to the Earth's core. High precision determination of the 182W isotopic composition of the Moon can help to resolve this issue. PMID:25114313

The effects of magmatic redistribution of heat producing elements on the lunar mantle evolution inferred from numerical models that start from various initial states

NASA Astrophysics Data System (ADS)

Ogawa, Masaki

2018-02-01

To discuss how redistribution of heat producing elements (HPEs) by magmatism affects the lunar mantle evolution depending on the initial condition, I present two-dimensional numerical models of magmatism in convecting mantle internally heated by incompatible HPEs. Mantle convection occurs beneath a stagnant lithosphere that inhibits recycling of the HPE-enriched crustal materials to the mantle. Magmatism is modeled by a permeable flow of magma generated by decompression melting through matrix. Migrating magma transports heat, mass, and HPEs. When the deep mantle is initially hot with the temperature TD around 1800 K at its base, magmatism starts from the beginning of the calculated history to extract HPEs from the mantle. The mantle is monotonously cooled, and magmatism ceases within 2 Gyr, accordingly. When the deep mantle is initially colder with TD around 1100 K, HPEs stay in the deep mantle for a longer time to let the planet be first heated up and then cooled only slightly. If, in addition, there is an HPE-enriched domain in the shallow mantle at the beginning of the calculation, magma continues ascending to the surface through the domain for more than 3 Gyr. The low TD models fit in with the thermal and magmatic history of the Moon inferred from spacecraft observations, although it is not clear if the models are consistent with the current understanding of the origin of the Moon and its magnetic field. Redistribution of HPEs by magmatism is a crucial factor that must be taken into account in future studies of the evolution of the Moon.

An ancient depleted mantle source for Archean crust in Rajasthan, India

NASA Technical Reports Server (NTRS)

Macdougall, J. D.; Gopalan, K.; Lugmair, G. W.; Roy, A. B.

1983-01-01

Data from an initial set of Banded Gneiss Complex (BGC) east of the city of Udaipur are given. In this region the BGC comprises typical grey gneiss with variably abundant granitic and mafic components. Efforts to date were concentrated on the mafic components which, based on chemical data, appear to be metavolcanic. All samples examined were recrystallized under amphibolite or upper amphibolite facies conditions. Pertinent chemical data for a small number of amphibolites analyzed so far are: SiO2: 49-53%; MgO: 5.7-7.3%; K2O: 0.24-0.50%; Ni: 106-140 ppm; Zr: 37-159 ppm. From Sm/Nd data, all amphibolites show small to moderate LREE enrichments.

Gakkel Ridge: A window to ancient asthenosphere

NASA Astrophysics Data System (ADS)

Snow, J.; Hellebrand, E.; Dick, H.; Liu, C.; Stracke, A.

2008-12-01

We are accustomed to thinking of the ambient mantle as being a well-stirred reservoir, which contains at most regions of stored subducted slabs and "plums" containing lithophile trace element enrichments. What is forgotten in all of this is that the main process of formation of heterogeneities is a negative one - generating 10x more depleted mantle at any given moment than it does oceanic crust. Because the volume of lithosphere subducted over Earth history is so large, it has always been assumed that the process of subduction and convective mixing re-homogenizes the depleted and enriched reservoirs about as fast as it produces them. What if it doesn't? Our primary means of studying mantle heterogeneity however is basalts. Direct study of the mantle entails observations on xenoliths, ophiolites and orogenic lherzolites, and abyssal peridotites. The latter have the inherent problems of being melting residues, associated with fracture zones, are highly serpentinized and rare. The arctic ridge system gives us a unique perspective on the mantle, and samples we have recovered there are relatively free from these problems. Due to the slow spreading rate, which apparently severely limits the melt productivity, the thickest crust in the Arctic ridge system is approximately "normal". The most common crust is about half thickness and there are large expanses with no crust at all, in the sense of Hess, 1962, exposing mantle peridotite in the floor of extensive rift zones. We have shown Os isotopic evidence for the survival of ancient depletion signatures in Gakkel abyssal peridotites that apparently were not destroyed by subduction, convective stirring or resetting during magma genesis (Liu, et al., 2008). Additionally, preliminary Nd isotopic evidence suggests at least a 400Ma intact prehistory for these samples. Apparently, the low melt productivity on Gakkel Ridge has allowed the Gakkel mantle rocks to escape significant resetting due to melt interaction. This implies a very different picture of the mantle from the one above, one where nearly every part of the mantle has an ancient history prior to its incorporation into the lithosphere, and the distribution of heterogeneities (enriched and depleted) into small scale regions that only approximate the bulk mantle on average (Meibom and Anderson, 2004). Sampling of that mantle by basalts cannot test this hypothesis. Sampling of mantle directly may do so. What this means is that every region of mantle sampled on magma starved ridges may contain traces of a previous history of depletion going far back in geologic time.

The subcontinental mantle beneath southern New Zealand, characterised by helium isotopes in intraplate basalts and gas-rich springs

NASA Astrophysics Data System (ADS)

Hoke, L.; Poreda, R.; Reay, A.; Weaver, S. D.

2000-07-01

New helium isotope data measured in Cenozoic intraplate basalts and their mantle xenoliths are compared with present-day mantle helium emission on a regional scale from thermal and nonthermal gas discharges on the South Island of New Zealand and the offshore Chatham Islands. Cenozoic intraplate basaltic volcanism in southern New Zealand has ocean island basalt affinities but is restricted to continental areas and absent from adjacent Pacific oceanic crust. Its distribution is diffuse and widespread, it is of intermittent timing and characterised by low magma volumes. Most of the 3He/ 4He ratios measured in fluid inclusions in mantle xenocrysts and basalt phenocrysts such as olivine, garnet, and amphibole fall within the narrow range of 8.5 ± 1.5 Ra (Ra is the atmospheric 3He/ 4He ratio) with a maximum value of 11.5 Ra. This range is characteristic of the relatively homogeneous and degassed upper MORB-mantle helium reservoir. No helium isotope ratios typical of the lower less degassed mantle (>12 Ra), such as exemplified by the modern hot-spot region of Hawaii (with up to 32 Ra) were measured. Helium isotope ratios of less than 8 Ra are interpreted in terms of dilution of upper mantle helium with a radiogenic component, due to either age of crystallisation or small-scale mantle heterogeneities caused by mixing of crustal material into the upper mantle. The crude correlation between age of samples and helium isotopes with generally lower R/Ra values in mantle xenoliths compared with host rock phenocrysts and the in general depleted Nd and Sr isotope ratios and the light rare earth element enrichment of the basalts supports derivation of melts as small melt fractions from a depleted upper mantle, with posteruptive ingrowth of radiogenic helium as a function of lithospheric age. In comparison, the regional helium isotope survey of thermal and nonthermal gas discharges of the South Island of New Zealand shows that mantle 3He anomalies in general do not show an obvious relationship with either age or proximity to the Cenozoic intraplate volcanic centres or with major faults. In general, areas characterised by mantle 3He emission are interpreted to define those regions beneath which mantle melting and basalt magma addition to the crust are recent. The strongest mantle 3He anomaly (equivalent to >80% mantle helium component) is centred over southern Dunedin, measured in magmatic CO 2-rich mineral water springs issuing from crystalline basement rocks which outcrop at the southern extent of Miocene intraplate basaltic volcanism which ceased 9 Ma ago. This mantle helium anomaly overlaps with an area characterised by elevated surface high heat flow, compatible with a long-lived mantle melt/heat input into the crust. In comparison Banks Peninsula, another Miocene intraplate basaltic centre, is characterised by relatively low surface heat flow and a small mantle helium contribution measured in a nitrogen-rich spring. Here the thermal transient induced by the magmatic event has either dissipated or has not reached the surface. In the former case one might be dealing with storage and mixing of magmatic and crustal gases at shallow crustal levels and in the latter with active to recent mantle-melt degassing at depth. Along the most actively deforming part of the plate boundary zone, the transpressional Alpine Fault and Marlborough fault systems, mantle helium is present in gas-rich springs in all those areas underlain by actively subducting oceanic crust (the Australian plate in the south and Pacific plate in the north), whereas the central part of the Alpine transpressional fault is characterised by pure crustal radiogenic helium. Areas where the mantle helium component is negligible are restricted to the centre part of the South Island, extending along its length from Southland to northern Canterbury and Murchison. These areas are interpreted to delineate the extent of thicker and colder lithosphere compared to all other areas where mantle helium release from partial mantle melts at depth is recent to active being added to the lower lithosphere and/or lower crust. Areas characterised by mantle helium anomalies are equated with areas of thermal mantle anomalies, i.e., localised mantle heterogeneities such as upwelling less dense silicate melts in the upper asthenospheric mantle.

Oxygen isotope geochemistry of mafic phenocrysts in primitive mafic lavas from the southernmost Cascade Range, California

USGS Publications Warehouse

Underwood, Sandra J.; Clynne, Michael A.

2017-01-01

Previously reported whole-rock δ18O values (5.6–7.8‰) for primitive quaternary mafic lavas from the southernmost Cascades (SMC) are often elevated (up to 1‰) relative to δ18O values expected for mafic magmas in equilibrium with mantle peridotite. Olivine, clinopyroxene, and plagioclase crystals were separated from 29 geochemically well-characterized mafic lavas for δ18O measurements by laser fluorination to assess modification of the mantle sources by ancient and modern subducted components. Oxygen isotope values of olivine phenocrysts in calc-alkaline lavas and contemporaneous high alumina olivine tholeiitic (HAOT) lavas generally exceed depleted mantle olivine values (~4.9–5.3‰). Modern addition of up to 6 wt% slab-derived fluid from Gorda serpentinized peridotite dehydration (~15‰) or chlorite dehydration (~10‰) within the serpentinized peridotite can provide the 18O enrichment detected in olivine phenocrysts (δ18Oolivine = 5.3–6.3‰) in calc-alkaline mafic lavas, and elevate 18O in overlying mantle lithosphere, as well. Specifically, although HAOT δ18Oolivine values (5.5–5.7‰) may reflect partial melting in heterogeneous 18O enriched mantle source domains that developed during multiple subduction events associated with terrane accretion (e.g., <1 wt% of ~15‰ materials), an additional 18O enrichment of up to 2 wt% of 10–15‰ slab-derived hydrous fluids might be accommodated. The calc-alkaline primitive magmas appear to have experienced a continuous range of open system processes, which operate in the mantle and during rapid magma ascent to eruption, and occasionally post quench. Textural relationships and geochemistry of these lava samples are consistent with blends of mafic phenocrysts and degassed melts in varying states of 18O disequilibrium. In lenses of accumulated melt within peridotite near the base of the crust, coexisting olivine and clinopyroxene δ18O values probably are not at isotopic equilibrium because fluids introduced into the system perturbed the δ18Omelt values. A “sudden” melt extraction event interrupts 18O equilibration in phenocrysts and poorly mixed melt(s). Rapid ascent of volatile oversaturated primitive mafic magma through the crust appears to be accompanied by devolatilization and crystallization of anorthite-rich plagioclase with elevated δ18Oplag values. The (Sr/P)N values for the whole rock geochemistry are consistent with a 87Sr/86Sr ~0.7027 slab-derived fluid addition into the infertile peridotite source of magmas, and melt devolatilization is recorded in the mixture of disequilibrium δ18O values for the constituent phases of lavas. Morbidity of the Gorda Plate as it undergoes intense deformation from the spreading ridge to the trench is likely a key factor to developing the carrying capacity of hydrous fluids and mineral phases in the slab subducting into the SMC mantle.

Geochemistry and petrogenesis of lava flows around Linga, Chhindwara area in the Eastern Deccan Volcanic Province (EDVP), India

NASA Astrophysics Data System (ADS)

Ganguly, Sohini; Ray, Jyotisankar; Koeberl, Christian; Saha, Abhishek; Thöni, Martin; Balaram, V.

2014-09-01

Based on systematic three-tier arrangement of vesicles, entablature and columnar joints, three distinct quartz normative tholeiitic lava flows (I, II and III) were recognized in the area around Linga, in the Eastern Deccan Volcanic Province (EDVP). Each of the flows exhibits intraflow chemical variations marked by high Mg#-low Ti, and low Mg#-high Ti contents. The MgO (4.27-7.74 wt.%), Mg# (23.45-41.89) and Zr (161.5-246.3 ppm) of Linga flows suggest an evolved chemistry marked by fractional crystallization and crustal contamination processes. Positive Rb and Th anomalies, negative Nb anomalies, relative enrichment of LILE-LREE with respect to Nb, Nb/Th:3.71-6.77 indicate crustal contamination of magma by continental materials through magma-crust interaction during melt migration and contributions from sub-continental lithospheric mantle (SCLM). Negative K, Sr and Ti anomalies corroborate an intracontinental, rift-controlled tectonic setting for the genesis and evolution of Linga basalts. Chondrite-normalized REE patterns reflect low HREE abundances and prominent LREE/HREE, MREE/HREE fractionation thereby pointing towards partial melting of garnet peridotite mantle source. Nb, Zr, Y variations suggest 10-15% partial melting of mantle source for the derivation of parent tholeiitic melt that suffered crystal fractionation of phenocrystal phases and subsequent liquid immiscibility. Critical evaluation of Srinitial and Ndinitial (65 Ma) isotopic compositions (87Sr/86Srinitial between 0.705656 and 0.706980 and 143Nd/144Ndinitial between 0.512523 and 0.512598) suggests that these basalts were derived from an enriched mantle (∼EM I-EM II) source. The εSr (21.84-41.27) and εNd (-0.28 to 1.10) isotopic signatures defined by higher εSr and lower εNd fingerprint a plume-related source. Positive and negative values of εNd indicate an isotopically heterogeneous mantle source marked by mixing of depleted (DM) and enriched mantle (EM I-EM II) components at the source region and together with 87Sr/86Srinitial ranging from 0.705656 to 0.706980 suggest two stage contamination of parent magma which is much similar to that of Poladpur, Toranmal, Mhow, Chikaldara flows. Ba/Y versus 87Sr/86Sr and Nb/Y versus Rb/Y variations show an Ambenali-Poladpur contamination trend for the Linga basalts thereby suggesting the role of upper continental granitic crust as the contaminant of these flows through magma-crust interaction during melt migration. The lava flows of Linga are geochemically correlatable with the Poladpur flows of southwestern and Toranmal flows of northern Deccan and show genetic coherence with the basalts of Jabalpur, Seoni, Chakhla-Delakhari of eastern Deccan.

Osmium isotope constraints on ore metal recycling in subduction zones

PubMed

McInnes; McBride; Evans; Lambert; Andrew

1999-10-15

Veined peridotite xenoliths from the mantle beneath the giant Ladolam gold deposit on Lihir Island, Papua New Guinea, are 2 to 800 times more enriched in copper, gold, platinum, and palladium than surrounding depleted arc mantle. Gold ores have osmium isotope compositions similar to those of the underlying subduction-modified mantle peridotite source region, indicating that the primary origin of the metals was the mantle. Because the mantle is relatively depleted in gold, copper, and palladium, tectonic processes that enhance the advective transport and concentration of these fluid soluble metals may be a prerequisite for generating porphyry-epithermal copper-gold deposits.

Mantle-derived trace element variability in olivines and their melt inclusions

NASA Astrophysics Data System (ADS)

Neave, David A.; Shorttle, Oliver; Oeser, Martin; Weyer, Stefan; Kobayashi, Katsura

2018-02-01

Trace element variability in oceanic basalts is commonly used to constrain the physics of mantle melting and the chemistry of Earth's deep interior. However, the geochemical properties of mantle melts are often overprinted by mixing and crystallisation processes during ascent and storage. Studying primitive melt inclusions offers one solution to this problem, but the fidelity of the melt-inclusion archive to bulk magma chemistry has been repeatedly questioned. To provide a novel check of the melt inclusion record, we present new major and trace element analyses from olivine macrocrysts in the products of two geographically proximal, yet compositionally distinct, primitive eruptions from the Reykjanes Peninsula of Iceland. By combining these macrocryst analyses with new and published melt inclusion analyses we demonstrate that olivines have similar patterns of incompatible trace element (ITE) variability to the inclusions they host, capturing chemical systematics on intra- and inter-eruption scales. ITE variability (element concentrations, ratios, variances and variance ratios) in olivines from the ITE-enriched Stapafell eruption is best accounted for by olivine-dominated fractional crystallisation. In contrast, ITE variability in olivines and inclusions from the ITE-depleted Háleyjabunga eruption cannot be explained by crystallisation alone, and must have originated in the mantle. Compatible trace element (CTE) variability is best described by crystallisation processes in both eruptions. Modest correlations between host and inclusion ITE contents in samples from Háleyjabunga suggest that melt inclusions can be faithful archives of melting and magmatic processes. It also indicates that degrees of ITE enrichment can be estimated from olivines directly when melt inclusion and matrix glass records of geochemical variability are poor or absent. Inter-eruption differences in olivine ITE systematics between Stapafell and Háleyjabunga mirror differences in melt inclusion suites, and confirm that the Stapafell eruption was fed by lower degree melts from greater depths within the melting region than the Háleyjabunga eruption. Although olivine macrocrysts from Stapafell are slightly richer in Ni than those from Háleyjabunga, their overall CTE systematics (e.g., Ni/(Mg/Fe), Fe/Mn and Zn/Fe) are inconsistent with being derived from olivine-free pyroxenites. However, the major element systematics of Icelandic basalts require lithological heterogeneity in their mantle source in the form of Fe-rich and hence fusible domains. We thus conclude that enriched heterogeneities in the Icelandic mantle are composed of modally enriched, yet nonetheless olivine-bearing, lithologies and that olivine CTE contents provide an incomplete record of lithological heterogeneity in the mantle. Modally enriched peridotites may therefore play a more important role in oceanic magma genesis than previously inferred.

Petrological constraints on evolution of continental lithospheric mantle beneath the northwestern Ethiopian plateau: Insight from mantle xenoliths from the Gundeweyn area, East Gojam, Ethiopia

NASA Astrophysics Data System (ADS)

Alemayehu, Melesse; Zhang, Hong-Fu; Zhu, Bin; Fentie, Birhanu; Abraham, Samuel; Haji, Muhammed

2016-01-01

Detailed petrographical observations and in-situ major- and trace-element data for minerals from ten spinel peridotite xenoliths from a new locality in Gundeweyn area, East Gojam, have been examined in order to understand the composition, equilibrium temperature and pressure conditions as well as depletion and enrichment processes of continental lithospheric mantle beneath the Ethiopian plateau. The peridotite samples are very fresh and, with the exception of one spinel harzburgite, are all spinel lherzolites. Texturally, the xenoliths can be divided into two groups as primary and secondary textures. Primary textures are protogranular and porphyroclastic while secondary ones include reaction, spongy and lamellae textures. The Fo content of olivine and Cr# of spinel ranges from 86.5 to 90.5 and 7.7 to 14.1 in the lherzolites, respectively and are 89.8 and 49.8, respectively, in the harzburgite. All of the lherzolites fall into the lower Cr# and Fo region in the olivine-spinel mantle array than the harzburgite, which indicates that they are fertile peridotites that experienced low degrees of partial melting and melt extraction. Orthopyroxene and clinopyroxene show variable Cr2O3 and Al2O3 contents regardless of their lithology. The Mg# of orthopyroxene and clinopyroxene are 87.3 to 90.1 and 85.8 to 90.5 for lherzolite and 90.4 and 91.2 for harzburgite, respectively. The peridotites have been equilibrated at a temperature and pressure ranging from 850 to 1100 °C and 10.2 to 30 kbar, respectively, with the highest pressure record from the harzburgite. They record high mantle heat flow between 60 and 150 mW/m2, which is not typical for continental environments (40 mW/m2). Such a high geotherm in continental area shows the presence of active mantle upwelling beneath the Ethiopian plateau, which is consistent with the tectonic setting of nearby area of the Afar plume. Clinopyroxene of five lherzolites and one harzburgite samples have a LREE enriched pattern and the rest exhibit LREE depletion relative to HREE. These suggest that the lithospheric mantle of the Ethiopian plateau has experienced at least two major processes, specifically, partial melting and metasomatism that produce LREE-depleted and -enriched signature of continental lithospheric mantle, respectively. There is also no clear relationship between degree of LREE enrichment and petrography of the studied peridotite. Based on our data, we conclude that the lithospheric mantle beneath Gundeweyn has experienced melt extraction during and/or before pan-African orogeny and then interacted with various degrees of asthenospheric melt. The interaction is probably related to mantle upwelling, which is mainly focused beneath East Africa rift system (EARS).

Rethinking Recycling in Arcs

NASA Astrophysics Data System (ADS)

Kelemen, P.; Behn, M. D.; Jagoutz, O.

2012-12-01

Hacker et al EPSL 2011 and Behn et al Nature Geosci 2011 investigated pathways for return of buoyant, subducted material to arc crust. These include (1) diapirs rising into the hot mantle wedge, with extensive melts adding a component to arc magmas, (2) flow of material back up a relatively cold "subduction channel", adding solids to the lower crust and small-degree partial melts to the upper crust, (3) flow from the forearc along the base of arc crust, and (4) imbrication of forearc material into arc crust. These processes add felsic, incompatible-element-rich components to arc crust. The flux of incompatible elements such as Th in arc lavas, thought to be mainly recycled from subducted sediments, is > sediment subduction flux. There are large uncertainties: arc crustal growth rates are imprecise; young, primitive arc lavas may not be representative of magmatic flux into arc crust; sediment subduction flux may have varied. Nevertheless, this result is found for all arcs examined, using recently published growth rates. Perhaps arc growth rates that include subduction erosion are systematically overestimated. Instead or in addition, maybe significant Th comes from material other than sediments. Here, we consider the implications of pathways 1-4 for arc growth rates and incompatible element enrichment, in the context of subduction erosion and arc-arc collision. Subducting arc lithologies can become separated, with only felsic components returned to arc crust. Buoyant lithologies are mobile in viscous instabilities at > 700-800°C. Whereas thin layers such as sediments may become mobile all at once, instabilities may periodically strip the hottest parts from the top of thick buoyant layers, replacing them with hot mantle. In arc-arc collision, the top of a subducting plate starts at about 0°C on the seafloor, so heating is slow. In subduction erosion, forearc material in the subducting package can be > 200°C before erosion so buoyant lithologies reach 700-800°C faster, and in larger volumes at a given time. Subduction erosion rarely, if ever, transports significant amounts of buoyant material deep into the convecting mantle. Because buoyant material can remain part of the crust, it may often be a mistake to add all of the eroded material to the observed arc volume to derive crustal growth rates. Buoyancy instabilities during subduction erosion or arc-arc collision will accumulate felsic arc crust. For example, > 50% of Aleutian arc lavas and exposed plutons are more buoyant than mantle peridotite at 700-800°C, 3-4 GPa. The buoyant material has an average of 60-62 wt% SiO2, molar Mg/(Mg+Fe) 0.4-0.5, and trace elements identical to bulk continental crust, though western Aleutian lavas have the most depleted Sr, Nd and Pb isotope ratios of all arc lavas worldwide. In general, density sorting of arc lithologies, and subsequent partial melting as buoyant rocks rise through the mantle wedge or along a subduction channel, could lead to a kind of double and triple distillation. Incompatible elements such as Th would be enriched in arc crust, retaining correlations with isotopic indicators of a recycled sediment component, while Th-poor, dense, mafic lavas and lower crustal cumulates return to the convecting mantle.

Mixed fluid sources involved in diamond growth constrained by Sr-Nd-Pb-C-N isotopes and trace elements

NASA Astrophysics Data System (ADS)

Klein-BenDavid, Ofra; Pearson, D. Graham; Nowell, Geoff M.; Ottley, Chris; McNeill, John C. R.; Cartigny, Pierre

2010-01-01

Sub-micrometer inclusions in diamonds carry high-density fluids (HDF) from which the host diamonds have precipitated. The chemistry of these fluids is our best opportunity of characterizing the diamond-forming environment. The trace element patterns of diamond fluids vary within a limited range and are similar to those of carbonatitic/kimberlitic melts that originate from beneath the lithospheric mantle. A convecting mantle origin for the fluid is also implied by C isotopic compositions and by a preliminary Sr isotopic study (Akagi, T., Masuda, A., 1988. Isotopic and elemental evidence for a relationship between kimberlite and Zaire cubic diamonds. Nature 336, 665-667.). Nevertheless, the major element chemistry of HDFs is very different from that of kimberlites and carbonatites, varying widely and being characterized by extreme K enrichment (up to ˜ 39 wt.% on a water and carbonate free basis) and high volatile contents. The broad spectrum of major element compositions in diamond-forming fluids has been related to fluid-rock interaction and to immiscibility processes. Elemental signatures can be easily modified by a variety of mantle processes whereas radiogenic isotopes give a clear fingerprint of the time-integrated evolution of the fluid source region. Here we present the results of the first multi radiogenic-isotope (Sr, Nd, Pb) and trace element study on fluid-rich diamonds, implemented using a newly developed off-line laser sampling technique. The data are combined with N and C isotope analysis of the diamond matrix to better understand the possible sources of fluid involved in the formation of these diamonds. Sr isotope ratios vary significantly within single diamonds. The highly varied but unsupported Sr isotope ratios cannot be explained by immiscibility processes or fluid-mineral elemental fractionations occurring at the time of diamond growth. Our results demonstrate the clear involvement of a mixed fluid, with one component originating from ancient incompatible element-enriched parts of the lithospheric mantle while the trigger for releasing this fluid source was probably carbonatitic/kimberlitic melts derived from greater depths. We suggest that phlogopite mica was an integral part of the enriched lithospheric fluid source and that breakdown of this mica releases K and radiogenic Sr into a fluid phase. The resulting fluids operate as a major metasomatic agent in the sub-continental lithospheric mantle as reflected by the isotopic composition and trace element patterns of G10 garnets.

Magma-derived CO2 emissions in the Tengchong volcanic field, SE Tibet: Implications for deep carbon cycle at intra-continent subduction zone

NASA Astrophysics Data System (ADS)

Zhang, Maoliang; Guo, Zhengfu; Sano, Yuji; Zhang, Lihong; Sun, Yutao; Cheng, Zhihui; Yang, Tsanyao Frank

2016-09-01

Active volcanoes at oceanic subduction zone have long been regard as important pathways for deep carbon degassed from Earth's interior, whereas those at continental subduction zone remain poorly constrained. Large-scale active volcanoes, together with significant modern hydrothermal activities, are widely distributed in the Tengchong volcanic field (TVF) on convergent boundary between the Indian and Eurasian plates. They provide an important opportunity for studying deep carbon cycle at the ongoing intra-continent subduction zone. Soil microseepage survey based on accumulation chamber method reveals an average soil CO2 flux of ca. 280 g m-2 d-1 in wet season for the Rehai geothermal park (RGP). Combined with average soil CO2 flux in dry season (ca. 875 g m-2 d-1), total soil CO2 output of the RGP and adjacent region (ca. 3 km2) would be about 6.30 × 105 t a-1. Additionally, we conclude that total flux of outgassing CO2 from the TVF would range in (4.48-7.05) × 106 t a-1, if CO2 fluxes from hot springs and soil in literature are taken into account. Both hot spring and soil gases from the TVF exhibit enrichment in CO2 (>85%) and remarkable contribution from mantle components, as indicated by their elevated 3He/4He ratios (1.85-5.30 RA) and δ13C-CO2 values (-9.00‰ to -2.07‰). He-C isotope coupling model suggests involvement of recycled organic metasediments and limestones from subducted Indian continental lithosphere in formation of the enriched mantle wedge (EMW), which has been recognized as source region of the TVF parental magmas. Contamination by crustal limestone is the first-order control on variations in He-CO2 systematics of volatiles released by the EMW-derived melts. Depleted mantle and recycled crustal materials from subducted Indian continental lithosphere contribute about 45-85% of the total carbon inventory, while the rest carbon (about 15-55%) is accounted by limestones in continental crust. As indicated by origin and evolution of the TVF volatiles, mantle-derived magmas at continental subduction zone can act as important triggers for liberation of carbon stored in crustal carbonate rocks, which has the potential to be a complement to volatile recycling mechanism at subduction zones. Variations in He-Nd-Sr isotopes of magmas and volatiles from different types of plate boundaries suggest higher amounts of recycled materials for mantle wedge enrichment of continental subduction zone relative to that of oceanic subduction zone.

Cainozoic Orogenic Magmatism In The Western-central Mediterranean Area: Implications For The Subduction-modified Mantle Sources

NASA Astrophysics Data System (ADS)

Beccaluva, L.; Bianchini, G.; Coltorti, M.; Siena, F.; Verde, M.

In this contribution new REE and Sr-Nd isotopic data carried out on Cainozoic subduction-related volcanic rocks from the western-central Mediterranean are dis- cussed within a general review of the Cainozoic orogenic magmatism of the area. These volcanic events are related to subduction processes which occurred along the Paleo-European margin at least since Eocene and migrated (trough passive sinking and slab roll-back) southeastward up to the present in the peri-Tyrrhenian margin of Italy. Orogenic rocks from Provence (34-20 Ma) are characterised by 87Sr/86Sr be- tween 0.70453 and 0.70579, and 143Nd/144Nd between 0.51292 and 0.51265, which are consistent with mantle sources modified by subduction fluids released by altered oceanic crust. Sr-Nd isotopic composition of orogenic rocks from Sardinia (32-13 Ma), show a more complex picture: some compositions with relatively low 87Sr/86Sr (<0.706) and high 143Nd/144Nd (>0.5125), are compatible with the subduction of pure oceanic crust, while compositions with very high 87Sr/86Sr (up to 0.7113) and low 143Nd/144Nd (down to 0.51219) require additional components of continental crust affinity in the mantle wedge (partial fusion of subducted terrigenous sediments?). As concerns the Aeolian volcanics (< 1.3 Ma), compositions are compatible with man- tle sources solely enriched by fluid components from subducted oceanic crust. How- ever, it is interesting to note that shoshonites from the younger series of Stromboli display distinctly higher 87Sr/86Sr (up to 0.7075) and lower 143Nd/144Nd composi- tion (down to 0.51242), thus requiring once again recycle of continental crust materials in their mantle sources. The influence of such continental crust-derived components appear to be even more important in the mantle sources of the Campania volcanics, where extreme Sr-Nd isotopic compositions are recorded (87Sr/86Sr up to 0.7097; 143Nd/144Nd down to 0.5122).

Using mineral geochemistry to decipher slab, mantle, and crustal inputs to the generation of high-Mg andesites from Mount Baker and Glacier Peak, northern Cascade arc

NASA Astrophysics Data System (ADS)

Sas, M.; DeBari, S. M.; Clynne, M. A.; Rusk, B. G.

2015-12-01

A fundamental question in geology is whether subducting plates get hot enough to generate melt that contributes to magmatic output in volcanic arcs. Because the subducting plate beneath the Cascade arc is relatively young and hot, slab melt generation is considered possible. To better understand the role of slab melt in north Cascades magmas, this study focused on petrogenesis of high-Mg andesites (HMA) and basaltic andesites (HMBA) from Mt. Baker and Glacier Peak, Washington. HMA have unusually high Mg# relative to their SiO2 contents, as well as elevated La/Yb and Dy/Yb ratios that are interpreted to result from separation of melt from a garnet-bearing residuum. Debate centers on the garnet's origin as it could be present in mineral assemblages from the subducting slab, deep mantle, thick lower crust, or basalt fractionated at high pressure. Whole rock analyses were combined with major, minor, and trace element analyses to understand the origin of these HMA. In the Tarn Plateau (Mt. Baker) flow unit (51.8-54.0 wt.% SiO2, Mg# 68-70) Mg#s correlate positively with high La/Yb in clinopyroxene equilibrium liquids, suggesting an origin similar to that of Aleutian adakites, where slab-derived melts interact with the overlying mantle to become Mg-rich and subsequently mix with mantle-derived basalts. The source for high La/Yb in the Glacier Creek (Mt. Baker) flow unit (58.3-58.7 wt.% SiO2, Mg# 63-64) is more ambiguous. High whole rock Sr/P imply origin from a mantle that was hydrated by an enriched slab component (fluid ± melt). In the Lightning Creek (Glacier Peak) flow unit (54.8-57.9 SiO2, Mg# 69-72) Cr and Mg contents in Cr-spinel and olivine pairs suggest a depleted mantle source, and high whole rock Sr/P indicate hydration-induced mantle melting. Hence Lightning Creek is interpreted have originated from a refractory mantle source that interacted with a hydrous slab component (fluid ± melt). Our results indicate that in addition to slab-derived fluids, slab-derived melts also have an important role in the production of HMA in the north Cascade arc.

Cobalt and precious metals in sulphides of peridotite xenoliths and inferences concerning their distribution according to geodynamic environment: A case study from the Scottish lithospheric mantle

NASA Astrophysics Data System (ADS)

Hughes, Hannah S. R.; McDonald, Iain; Faithfull, John W.; Upton, Brian G. J.; Loocke, Matthew

2016-01-01

Abundances of precious metals and cobalt in the lithospheric mantle are typically obtained by bulk geochemical analyses of mantle xenoliths. These elements are strongly chalcophile and the mineralogy, texture and trace element composition of sulphide phases in such samples must be considered. In this study we assess the mineralogy, textures and trace element compositions of sulphides in spinel lherzolites from four Scottish lithospheric terranes, which provide an ideal testing ground to examine the variability of sulphides and their precious metal endowments according to terrane age and geodynamic environment. Specifically we test differences in sulphide composition from Archaean-Palaeoproterozoic cratonic sub-continental lithospheric mantle (SCLM) in northern terranes vs. Palaeozoic lithospheric mantle in southern terranes, as divided by the Great Glen Fault (GGF). Cobalt is consistently elevated in sulphides from Palaeozoic terranes (south of the GGF) with Co concentrations > 2.9 wt.% and Co/Ni ratios > 0.048 (chondrite). In contrast, sulphides from Archaean cratonic terranes (north of the GGF) have low abundances of Co (< 3600 ppm) and low Co/Ni ratios (< 0.030). The causes for Co enrichment remain unclear, but we highlight that globally significant Co mineralisation is associated with ophiolites (e.g., Bou Azzer, Morocco and Outokumpu, Finland) or in oceanic peridotite-floored settings at slow-spreading ridges. Thus we suggest an oceanic affinity for the Co enrichment in the southern terranes of Scotland, likely directly related to the subduction of Co-enriched oceanic crust during the Caledonian Orogeny. Further, we identify a distinction between Pt/Pd ratio across the GGF, such that sulphides in the cratonic SCLM have Pt/Pd ≥ chondrite whilst Palaeozoic sulphides have Pt/Pd < chondrite. We observe that Pt-rich sulphides with discrete Pt-minerals (e.g., PtS) are associated with carbonate and phosphates in two xenolith suites north of the GGF. This three-way immiscibility (carbonate-sulphide-phosphate) indicates carbonatitic metasomatism is responsible for Pt-enrichment in this (marginal) cratonic setting. These Co and Pt-enrichments may fundamentally reflect the geodynamic setting of cratonic vs. non-cratonic lithospheric terranes and offer potential tools to facilitate geochemical mapping of the lithospheric mantle.

Regularities of spatial association of major endogenous uranium deposits and kimberlitic dykes in the uranium ore regions of the Ukrainian Shield

NASA Astrophysics Data System (ADS)

Kalashnyk, Anna

2015-04-01

During exploration works we discovered the spatial association and proximity time formation of kimberlite dykes (ages are 1,815 and 1,900 Ga for phlogopite) and major industrial uranium deposits in carbonate-sodium metasomatites (age of the main uranium ore of an albititic formation is 1,85-1,70 Ga according to U-Pb method) in Kirovogradsky, Krivorozhsky and Alekseevsko-Lysogorskiy uranium ore regions of the Ukrainian Shield (UkrSh) [1]. In kimberlites of Kirovogradsky ore region uranium content reaches 18-20 g/t. Carbon dioxide is a major component in the formation of hydrothermal uranium deposits and the formation of the sodium in the process of generating the spectrum of alkaline ultrabasic magmas in the range from picritic to kimberlite and this is the connection between these disparate geochemical processes. For industrial uranium deposits in carbonate-sodium metasomatitics of the Kirovogradsky and Krivorozhsky uranium ore regions are characteristic of uranyl carbonate introduction of uranium, which causes correlation between CO2 content and U in range of "poor - ordinary - rich" uranium ore. In productive areas of uranium-ore fields of the Kirovogradsky ore region for phlogopite-carbonate veinlets of uranium ore albitites deep δ13C values (from -7.9 to -6.9o/oo) are characteristic. Isotope-geochemical investigation of albitites from Novokonstantynovskoe, Dokuchaevskoe, Partyzanskoe uranium deposits allowed obtaining direct evidence of the involvement of mantle material during formation of uranium albitites in Kirovogradsky ore region [2]. Petrological characteristics of kimberlites from uranium ore regions of the UkrSh (presence of nodules of dunite and harzburgite garnet in kimberlites, diamonds of peridotite paragenesis, chemical composition of indicator minerals of kimberlite, in particular Gruzskoy areas pyropes (Cr2O3 = 6,1-7,1%, MgO = 19,33-20,01%, CaO = 4,14-4,38 %, the content of knorringite component of most grains > 50mol%), chromites (Cr2O3 = 45,32-62,17%, MgO = 7,3-12,5%) allow us to estimate the depth of generation of kimberlite magmas more than 170-200 km. Ilmenites show two groups according to MgO, Cr2O3 and TiO2 content. Reconstructions of the mantle sections show also two intervals of pressures divided at 4.5 GPa, the upper part is highly metasomatized This high degree metasomatism is determined for almost all mantle columns. It is suggested that large-scale of uranium-bearing mantle fluids may be associated with the ancient degasation during the subduction which is highly enriched in U component . Analysis of the reasons for the marked association kimberlitic dykes and major industrial uranium deposits in carbonate-sodium metasomatic in the UkrSh led to the conclusion that hydrothermal uranium deposits are confined to the supply mantle fluid systems of mantle fault zones exercising brings sodium carbonate solutions enriched uranium from mantle sources. References: 1. Kalashnik A.A. New prognostic-evaluation criteria in technology prognosis of forming industrial endogenous uranium deposits of the Ukrainian Shield, 2014. Scientific proceedings of UkrSGRI, № 2, p. 27-54 (in Russian) 2. Stepanjuk L.M., Bondarenko S.V., Somka V.O. and other, 2012. Source of uranium and uranium-bearing sodium albitites for example of Dokuchaievskogo field of the Ingulsky megablock of the UkrSh: Abstracts of scientific conference "Theoretical issues and research practice metasomatic rocks and ores" (Kyiv, 14-16 March 2012), IGMOF, p.78-80. (in Ukrainian)

Mantle reservoirs (EM-1, OIB, E-MORB and N-MORB), long duration and polystages history for PGE-bearing paleoproterozoic layered intrusions in the N-E part of Fennoscandian Shield.

NASA Astrophysics Data System (ADS)

Bayanova, Tamara; Nerovich, Ludmila; Serov, Pavel; Kunakkuzin, Evgeniy; Elizarov, Dmitriy

2015-04-01

Paleoproterozoic layered PGE -bearing intrusions located in the N-E part of the Fennoscandian Shield and have a total are about 2000 km2. Long multidisciplinary studies using isotope Nd-Sr, U-Pb and 3He/4He systematics permit create a big bank of geochemistry data for different part of the intrusions: barren and main Cu-Ni-Cr-Ti-V and PGE phases, dykes complexes and host rocks. Based on U-Pb isotope data (on baddeleyite and zircon) and Sm-Nd mineral isochrones (on rock-forming and sulphides minerals) there is distinguished long magmatic duration from 2.53 to 2.40 Ga. Using precise U-Pb and Sm-Nd data for different part of the intrusions there are established four main impulses: 2.53, 2.50, 2.45, and 2.40 Ga of magmatic (LIP) activities for gabbronorite, anothosite et.set. rocks. The primary reservoir for all precious and multimetal massifs are considered as enriched mantle EM-1 using ɛNd- ISr system with negative ɛNd values and low ISr data for whole rocks of the intrusions. Dyke complexes are presented as three groups: high Ti-ferrodolerites, low Ti and low Fe-gabbronorites. Complex isotope (U-Pb, Sm-Nd) and geochemistry (REE, ɛNd, ISr) data investigations reflect OIB, E-MORB and N-MORB reservoirs for its origin (Nerovich et all., 2014). Isotope 3He/4He and 3He concentrations for accessory minerals ( ilmenite, magnetite et. set ) from the layered paleoproterozoic intrusions reflect significant lower mantle component and upper mantle contribution. According to the model of binary mixing (Jahn et all, 2000) there were calculated mantle and core component into plume magmatic reservoir connected with the origin of the PGE paleoproterozoic intrusions. The mantle contributions lie in the interval from 85 to 93% and core component are very less. All investigations are devoted to memory of academician RAS, professor F.Mitrofanov (Russia), he was a leader of scientific school for geology, geochemistry and metallogenesis of ore deposits. The studies are contribution by RFBR OFI-M 13-05-12055, 13-05-00493, Department of Earth Sciences RAS (programs 2 and 4) and IGCP-SIDA 599.

Melt focusing and CO2 extraction at mid-ocean ridges: simulations of reactive two-phase flow

NASA Astrophysics Data System (ADS)

Keller, T.; Katz, R. F.; Hirschmann, M. M.

2016-12-01

The deep CO2 cycle is the result of fluxes between near-surface and mantle reservoirs. Outgassing from mid-ocean ridges is one of the primary fluxes of CO2 from the asthenosphere into the ocean-atmosphere reservoir. Focusing of partial melt to the ridge axis crucially controls this flux. However, the role of volatiles, in particular CO2 and H2O, on melt transport processes beneath ridges remains poorly understood. We investigate this transport using numerical simulations of two-phase, multi-component magma/mantle dynamics. The phases are solid mantle and liquid magma; the components are dunite, MORB, hydrated basalt, and carbonated basalt. These effective components capture accepted features of mantle melting with volatiles. The fluid-dynamical model is McKenzie's formulation [1], while melting and reactive transport use the R_DMC method [2,3]. Our results indicate that volatiles cause channelized melt transport, which leads to significant variability in volume and composition of focused melt. The volatile-induced expansion of the melting regime at depth, however, has no influence on melt focusing; distal volatile-rich melts are not focused to the axis. Up to 50% of these melts are instead emplaced along the oceanic LAB. There, crystallization of accumulated melt leads to enrichment of CO2 and H2O in the deep lithosphere, which has implications for LAB rheology and volatile recycling by subduction. Results from a suite of simulations, constrained by catalogued observational data [4,5,6] enable predictions of global MOR CO2 output. By combining observational constraints with self-consistent numerical simulations we obtain a range of CO2 output from the global ridge system of 28-110 Mt CO2/yr, corresponding to mean CO2 contents of 50-200 ppm in the mantle. REFERENCES[1] McKenzie (1984), doi:10.1093/petrology/25.3.713.[2] Rudge, Bercovici & Spiegelman (2011), doi:10.1111/j.1365-246X.2010.04870.x.[3] Keller & Katz (2016), doi:10.1093/petrology/egw030.[4] Dalton, Langmuir & Gale (2014), doi:10.1126/science.1249466.[5] Gale, Langmuir & Dalton (2014), doi:10.1093/petrology/egu017.[6] White et al. (2001), doi:10.1093/petrology/42.6.1171. Fig: Simulation results of MOR magma/mantle dynamics with H2O and CO2, showing Darcy flux magnitude for half-spreading rates of 1 and 5 cm/yr.

Petrogenesis of metaultramafic rocks from the Quadrilátero Ferrífero and adjacent terrains, Minas Gerais, Brazil: Two events of ultramafic magmatism?

NASA Astrophysics Data System (ADS)

da Fonseca, Gabriela Magalhães; Jordt-Evangelista, Hanna; Queiroga, Gláucia Nascimento

2018-03-01

In the worldwide known Quadrilátero Ferrífero and the adjacent terrains, southeastern Brazil, many serpentinite and soapstone quarries, and some rare bodies of metaultramafic rocks that partially preserve minerals or textures from the original igneous protolith can be found. It is not known if the protoliths and the ages of the metaultramafic rocks found in the Quadrilátero Ferrífero (and its oriental basement) and Mineiro Belt regions are the same or if they represent distinct magmatic episodes. The petrogenetic investigation, specially concerning the REE contents, aimed to gather informations about the type of magmatism and the mantle source in order to compare the metaultramafic rocks of both regions. The interpretation of the data concerning petrography, mineral chemistry and geochemistry shows that the metaultramafic rocks are similar to komatiitic peridotites, with MgO contents > 22 wt % and TiO2 < 0.9 wt %. The plot of the REE for the lithotypes found in the Quadrilátero Ferrífero shows decrease in LREE possibly reflecting the depletion of the mantle source. On the other hand the samples from the Mineiro Belt are enriched in LREE suggesting a mantle source enriched in these elements. This enrichment may have been caused by mantle metassomatism that occurred during accretion of the Paleoproterozoic magmatic arc that generated the Mineiro belt. In this paper, we therefore suggest two periods of ultramafic magmatism. The first one found in the Archean basement of the Quadrilátero Ferrífero, with a depleted mantle source. The second occurred in the Paleoproterozoic basement of the Mineiro belt, having a metassomatized mantle as source.

Os-186 and Os-187 Enrichments and High-He-3/He-4 sources in the Earth's Mantle: Evidence from Icelandic Picrites

NASA Technical Reports Server (NTRS)

Brandon, Alan D.; Graham, David W.; Waight, Tod; Gautason, Bjarni

2007-01-01

Picrites from the neovolcanic zones in Iceland display a range in Os-187/Os-188O from 0.1297 to 0.1381 ((gamma)Os = 0.0 to 6.5) and uniform Os-186/Os-188 of 0.1198375+/-32 (2 (sigma)). The value for Os-186/Os-188 is within uncertainty of the present-day value for the primitive upper mantle of 0.1198398+/-16. These Os isotope systematics are best explained by ancient recycled crust or melt enrichment in the mantle source region. If so, then the coupled enrichments displayed in Os-186/Os-188 and Os-187/Os-188 from lavas of other plume systems must result from an independent process, the most viable candidate at present remains core-mantle interaction. While some plumes with high He-3/He-4, such as Hawaii, appear to have been subjected to detectable addition of Os (and possibly He) from the outer core, others such as Iceland do not. A positive correlation between Os-187/Os-188 and He-3/He-4 from 9.6 to 19 RA in Iceland picrites is best modeled as mixtures of 500 Ma or older ancient recycled crust mixed with primitive mantle, creating a hybrid source region that subsequently mixes with the convecting MORB mantle during ascent and melting. This multistage mechanism to explain these isotope systematics is consistent with ancient recycled crust juxtaposed with more primitive, relatively He-rich mantle, in convective isolation from the upper mantle, most likely in the lowermost mantle. This is inconsistent with models that propose random mixing between heterogeneities in the convecting upper mantle as a mechanism to explain the observed isotopic variation in oceanic lavas or models that produce a high He-3/He-4 signature in melt depleted and strongly outgassed, He-poor mantle. Instead these systematics require a deep mantle source to explain the 3He/4He signature in Iceland lavas. The He-3/He-4 of lavas derived from the Iceland plume changed over time, from a maximum of 50 RA at 60 Ma, to approximately 25-27 RA at present. The changes are coupled with distinct compositional gaps between the different aged lavas when H-3/He-4 is plotted versus various geochemical parameters such as Nd-143/Nd-144 and La/Sm. These relationships can be interpreted as an increase in the proportion of ancient recycled crust in the upwelling plume over this time period.

Plume magmatism and crustal growth at 2.9 to 3.0 Ga in the Steep Rock and Lumby Lake area, Western Superior Province

NASA Astrophysics Data System (ADS)

Tomlinson, K. Y.; Hughes, D. J.; Thurston, P. C.; Hall, R. P.

1999-01-01

The greenstone belts of the western Superior Province are predominantly 2.78 to 2.69 Ga and provide evidence of oceanic and arc volcanism during the accretionary phase of development of the Superior Province. There is also scattered evidence of Meso-Archean crust (predominantly 2.9 to 3.0 Ga) within the western Superior Province. The Meso-Archean greenstone belts commonly contain platformal sediments and unconformably overlie granitoid basement. The platformal sediments occur associated with komatiitic and tholeiitic volcanic rocks that suggest a history of magmatism associated with rifting during the Meso-Archean. The central Wabigoon Subprovince is a key area of Meso-Archean crust and in its southern portion comprises the Steep Rock, Finlayson and Lumby Lake greenstone belts. The Steep Rock greenstone belt unconformably overlies 3 Ga continental basement and contains platformal sediments succeeded by komatiitic and tholeiitic volcanic rocks. The Lumby Lake greenstone belt contains thick sequences of mafic volcanics, a number of komatiite horizons, and thin platformal sedimentary units. The two belts are joined by the predominantly mafic volcanic Finlayson greenstone belt. The volcanics throughout these three greenstone belts may be correlated to some extent and a range of basaltic and komatiite types is present. Al-undepleted komatiites present in the Lumby Lake greenstone belt have an Al 2O 3/TiO 2 ratio ranging from 14 to 27 and (Gd/Yb) N from 0.7 to 1.3. These are divided into basaltic komatiites with generally unfractionated mantle-normalised multi-element profiles, and spinifex-textured high-Mg basalts with slightly light REE enriched multi-element profiles and small negative Nb and Ta anomalies. The unfractionated basaltic komatiites represent high degree partial melts of the upper mantle whereas the spinifex-textured high-Mg basalts represent evolutionary products of the komatiite liquids following olivine and chromite fractionation and crustal contamination. Al-depleted komatiites are present in both the Lumby Lake and Steep Rock belts and have Al 2O 3/TiO 2 ratio ranges from 2.5 to 5. These display strong enrichment in the light REE and Nb and strong depletion in the heavy REE and Y ((Gd/Yb) N=2-4). They represent a deep mantle plume source generated from a high degree of partial melting in the majorite garnet stability field. The basaltic flows in all three greenstone belts are predominantly slightly light REE depleted and represent a slightly depleted upper mantle source. Basalts spatially associated with the unfractionated basaltic komatiites and the slightly light REE enriched spinifex-textured high-Mg basalts are also slightly enriched in light REE and have negative Nb and Ta anomalies. These basalts represent evolved products of the primitive basaltic komatiites and enriched spinifex-textured high-Mg basalts after further crustal contamination and olivine and clinopyroxene fractionation. The geochemical stratigraphy in the Lumby Lake belt is consistent with an ascending mantle plume model. The light REE depleted basalts were derived from upper mantle melted by an ascending mantle plume. These are overlain by the unfractionated basaltic komatiites and their evolutionary products which represent hotter plume head material derived from a mixture of plume mantle and entrained depleted upper mantle. In turn, these are overlain by strongly light REE and HFSE enriched komatiites that represent a deep plume source that has not been mixed with depleted mantle and are, therefore, likely to have been derived from a plume core or tail. Volcanism was protracted in these three greenstone belts lasting ca. 70 Ma and combined stratigraphic evidence from the Lumby Lake and Steep Rock belts suggests that more than one plume may have ascended and tapped the same mantle sources, over time, within the area. Plume magmatism and rifting of continental platforms thus appears to have been an important feature of crustal development in the Meso-Archean.

Melting and Its Influence on the Long-term Evolution of the Lower Mantle Heterogeneities (LLSVP and ULVZ)

NASA Astrophysics Data System (ADS)

Fomin, I.; Tackley, P. J.

2017-12-01

Recent investigations have shown mantle solidus close to the range of proposed core-mantle boundary (CMB) temperatures (e.g. [Andrault et al., 2011, 2014], [de Koker et al., 2013]). Certain fraction of distinct rocks may reduce the effective melting temperature to values below the CMB temperature. It is especially true for iron enriched materials such as MORB [Nomura et al., 2011], BIF [Kato et al., 2016], iron-rich periclase [Boukare et al., 2015] and other rock species used to explain observed seismic anomalies. Computer simulations allow to study evolution and stability for chemically distinct piles proposed from geophysical data. Previous researches (e.g. [Mulyukova et al., 2015]) found those piles stirring in several hundreds of Ma. Our investigation adds influence of melting and following chemical differentiation on preservation of such structures.We present StagYY code [Tackley et al., 2008] with extended set of routines to model melting, melt redistribution and melt-dependent rheology in addition to solid-state mantle convection to reveal fate of chemically distinct piles in long-term (millions of years) perspective. A new point of our approach is usage of chemically independent oxides to describe rock composition and physical properties. Thin layers homogenize in few tens of millions of years despite whether melting happens or not. Thick structures (like periclase piles proposed for ULVZ [Wicks et al., 2010] or MORB-bearing domes for LLSVP [Ohta et al., 2008]) undergo partial melting if CMB temperature is above 3700K. Melt migration results in extraction of fusible components and therefore segregation of iron-enriched material. However, we weren't able to obtain any stabilized layer of iron-rich partially molten material at the CMB, because ongoing interaction and reequilibration of melt and solid results in buoyant liquids spreading to the adjacent mantle. Rheological influence of melt on bulk rock properties reduces time pile can exist.Our modeling puts severe constraints on the presence and fate of chemical heterogeneities in the lowermost mantle. Melting enhances stirring of such heterogeneities and generally no silicate melt can be stabilized at CMB for long time. Only low CMB temperatures (generally lower than 3700 K) allow anomalies to exist for geological periods of time (hundreds of Ma).

Helium in the Archean komatiites revisited: significantly high 3He/ 4He ratios revealed by fractional crushing gas extraction

NASA Astrophysics Data System (ADS)

Matsumoto, Takuya; Seta, Akihiro; Matsuda, Jun-ichi; Takebe, Masamichi; Chen, Yuelong; Arai, Shoji

2002-03-01

In order to provide constraints on 3He/ 4He ratios in the Archean mantle source, we have analyzed helium isotopic compositions in 2.7 Ga old Archean komatiites from the Abitibi green stone belt, Ontario, Canada. Two spinifex-textured komatiites yielded significantly high 3He/ 4He ratios of about 30 Ra (where Ra denotes the atmospheric 3He/ 4He ratio) in fractions released by sequential crushing. These results are the first confirmation of the occurrence of high 3He/ 4He ratios in Archean komatiites after the intriguing finding by Richard et al. [Science 273 (1996) 93-95] in komatiites from a nearby locality, Alexo. We also found that the crystal structure of the komatiites was significantly enriched in a radiogenic component ( 4He) and that this 4He was actually degassed by crushing gas extraction, indicating that the nominal 3He/ 4He ratios measured by crushing are lower limits for the 3He/ 4He ratio of the intrinsic component. By constraining the release behavior of radiogenic 4He by crushing, we have estimated the initial 3He/ 4He ratio of the inclusion-trapped component to be 73.0 +7.8-5.5 Ra. A mantle source with such a high 3He/ 4He ratio at 2.7 Ga, if evolved in a closed system, would have a present-day 3He/ 4He ratio of 46-60 Ra, indicating that the komatiites from Munro have trapped their helium from a mantle reservoir with a very high 3He/ 4He ratio in the context of the present-day value. However, whether or not such a source can be considered as equivalent to the primitive mantle source (such that sampled at hotspots) is highly model-dependent. If a closed system evolution model is assumed, helium in the Munro komatiites is not likely to be derived from the mid-ocean ridge basalt (MORB) source-like reservoir. However, the notion that the komatiites may be derived from a depleted reservoir in terms of trace elemental and isotopic geochemistry might require an alternative view for the 3He/ 4He evolution in ancient mantle reservoirs, as has been demonstrated by a recent model calculation by Seta et al. [Earth Planet. Sci. Lett. 188 (2001) 211-219] in which the 3He/ 4He ratios in the MORB mantle source could have been as high as those in the primitive (less degassed) mantle source in the Archean.

Origin and evolution of the Ilmeny-Vishnevogorsky carbonatites (Urals, Russia): insights from trace-element compositions, and Rb-Sr, Sm-Nd, U-Pb, Lu-Hf isotope data

NASA Astrophysics Data System (ADS)

Nedosekova, I. L.; Belousova, E. A.; Sharygin, V. V.; Belyatsky, B. V.; Bayanova, T. B.

2013-02-01

The carbonatites of the Ilmeny-Vishnevogorsky Alkaline Complex (IVAC) are specific in geological and geochemical aspects and differ by some characteristics from classic carbonatites of the zoned alkaline-ultramafic complexes. Geological, geochemical and isotopic data and comparison with relevant experimental systems show that the IVAC carbonatites are genetically related to miaskites, and seem to be formed as a result of separation of carbonatite liquid from a miaskitic magma. Appreciable role of a carbonate fluid is established at the later stages of carbonatite formation. The trace element contents in the IVAC carbonatites are similar to carbonatites of the ultramafic-alkaline complexes. The characteristic signatures of the IVAC carbonatites are a high Sr content, a slight depletion in Ba, Nb, Та, Ti, Zr, and Hf, and enrichment in HREE in comparison with carbonatites of ultramafic-alkaline complexes. This testifies a specific nature of the IVAC carbonatites related to the fractionation of a miaskitic magma and to further Late Paleozoic metamorphism. Isotope data suggest a mantle source for IVAC carbonatites and indicate that moderately depleted mantle and enriched EMI-type components participated in magma generation. The lower crust could have been involved in the generation of the IVAC magma.

Eruption style at Kīlauea Volcano in Hawai‘i linked to primary melt composition

USGS Publications Warehouse

Sides. I.R.,; Edmonds, M.; Maclennan, J.; Swanson, Don; Houghton, Bruce F.

2014-01-01

Explosive eruptions at basaltic volcanoes have been linked to gas segregation from magmas at shallow depths in the crust. The composition of primary melts formed at greater depths was thought to have little influence on eruptive style. Ocean island basaltic volcanoes are the product of melting of a geochemically heterogeneous mantle plume and are expected to give rise to heterogeneous primary melts. This range in primary melt composition, particularly with respect to the volatile components, will profoundly influence magma buoyancy, storage and eruption style. Here we analyse the geochemistry of a suite of melt inclusions from 25 historical eruptions at the ocean island volcano of Kīlauea, Hawai‘i, over the past 600 years. We find that more explosive styles of eruption at Kīlauea Volcano are associated statistically with more geochemically enriched primary melts that have higher volatile concentrations. These enriched melts ascend faster and retain their primary nature, undergoing little interaction with the magma reservoir at the volcano’s summit. We conclude that the eruption style and magma-supply rate at Kīlauea are fundamentally linked to the geochemistry of the primary melts formed deep below the volcano. Magmas might therefore be predisposed towards explosivity right at the point of formation in their mantle source region.

Geochemical constraints on depth of origin of oceanic carbonatites: The Cape Verde case

NASA Astrophysics Data System (ADS)

Doucelance, Régis; Hammouda, Tahar; Moreira, Manuel; Martins, João C.

2010-12-01

We present new Sr-Nd isotope compositions together with major- and trace element concentrations measured for whole rocks and mineral separate phases (apatite, biotite and calcite) from fifteen Cape Verde oceanic carbonatites (Atlantic Ocean). Trace element patterns of calcio- and magnesio-carbonatites present a strong depletion in K, Hf, Zr and Ti and an overall enrichment in Sr and REE relative to Cape Verde basalts, arguing for distinct source components between carbonatites and basalts. Sr and Nd isotopic ratios show small, but significant variations defining a binary mixing between a depleted end-member with unradiogenic Sr and radiogenic Nd values and a ''enriched'' end-member compatible with old marine carbonates. We interpret the depleted end-member as the Cape Verde oceanic lithosphere by comparison with previous studies on Cape Verde basalts. We thus propose that oceanic carbonatites are resulting from the interaction of a deep rooted mantle plume carrying a lower 4He/ 3He signature from the lower mantle and a carbonated metasomatized lithosphere, which by low degree melting produced carbonatite magmas. Sr-Nd compositions and trace element patterns of carbonatites argue in favor of a metasomatic agent originating from partial melting of recycled, carbonated oceanic crust. We have successfully reproduced the main geochemical features of this model using a Monte-Carlo-type simulation.

Role of melting process and melt-rock reaction in the formation of Jurassic MORB-type basalts (Alpine ophiolites)

NASA Astrophysics Data System (ADS)

Renna, Maria Rosaria; Tribuzio, Riccardo; Sanfilippo, Alessio; Thirlwall, Matthew

2018-04-01

This study reports a geochemical investigation of two thick basalt sequences, exposed in the Bracco-Levanto ophiolite (northern Apennine, Italy) and in the Balagne ophiolite (central-northern Corsica, France). These ophiolites are considered to represent an oceanward and a continent-near paleogeographic domain of the Jurassic Liguria-Piedmont basin. Trace elements and Nd isotopic compositions were examined to obtain information about: (1) mantle source and melting process and (2) melt-rock reactions during basalt ascent. Whole-rock analyses revealed that the Balagne basalts are slightly enriched in LREE, Nb, and Ta with respect to the Bracco-Levanto counterparts. These variations are paralleled by clinopyroxene chemistry. In particular, clinopyroxene from the Balagne basalts has higher CeN/SmN (0.4-0.3 vs. 0.2) and ZrN/YN (0.9-0.6 vs. 0.4-0.3) than that from the Bracco-Levanto basalts. The basalts from the two ophiolites have homogeneous initial Nd isotopic compositions (initial ɛ Nd from + 8.8 to + 8.6), within typical depleted mantle values, thereby excluding an origin from a lithospheric mantle source. These data also reject the involvement of contaminant crustal material, as associated continent-derived clastic sediments and radiolarian cherts have a highly radiogenic Nd isotopic fingerprint ( ɛ Nd at the time of basalt formation = - 5.5 and - 5.2, respectively). We propose that the Bracco-Levanto and the Balagne basalts formed by partial melts of a depleted mantle source, most likely containing a garnet-bearing enriched component. The decoupling between incompatible elements and Nd isotopic signature can be explained either by different degrees of partial melting of a similar asthenospheric source or by reaction of the ascending melts with a lower crustal crystal mush. Both hypotheses are reconcilable with the formation of these two basalt sequences in different domains of a nascent oceanic basin.

Origin and Distribution of Water Contents in Continental and Oceanic Lithospheric Mantle

NASA Technical Reports Server (NTRS)

Peslier, Anne H.

2013-01-01

The water content distribution of the upper mantle will be reviewed as based on the peridotite record. The amount of water in cratonic xenoliths appears controlled by metasomatism while that of the oceanic mantle retains in part the signature of melting events. In both cases, the water distribution is heterogeneous both with depth and laterally, depending on localized water re-enrichments next to melt/fluid channels. The consequence of the water distribution on the rheology of the upper mantle and the location of the lithosphere-asthenosphere boundary will also be discussed.

Characterizing slab inputs in the earliest stages of subduction: Preliminary evidence from fluid-mobile element systematics for IODP Expedition 352 recovered volcanic samples

NASA Astrophysics Data System (ADS)

Sanatan, Keir; Ryan, Jeffrey; Atlas, Zachary; Reagan, Mark

2016-04-01

IODP Expedition 352 recovered ~1.22 km of boninitic and basaltic volcanic rocks from four sites in the Izu-Bonin forearc to examine the volcanic phenomena associated with subduction initiation. While the recovered forearc basalts give little indication for the involvement of slab-derived volatiles, the extensive sequences of boninite series lavas recovered up-section show physical evidence for extensive fluid involvement (heavy vesicularity, explosive eruptive style), along with chemistries indicative of fluid-addition melting of depleted mantle sources. We are attempting to assay the makeup and likely slab provenance of these fluids via their fluid-mobile element (B, As, Cs, Sb, Pb, Li) systematics. Boron abundances measured thus far in fresh boninitic glasses recovered from Holes U1439C and U1442A range from 3-12 ppm, with B/Be and B/La ranging from 7.5-106 and 2-18.5, respectively. While the highest values are comparable to those observed in the most B-enriched Izu-bonin arc rocks, most of the data are at the low end of this range. Cs/Th and Pb/Ce ratios encompass the range of values encountered in IBM boninites in the literature, and are comparable to values for Izu arc lavas, while As/Sm ratios appear to be lower than in arc suites. Li concentrations are elevated relative to basaltic lavas, at 7-17 ppm, and Li/Yb ratios range from 8-22, a factor of four higher than the range encountered in volcanic arc suites. While fluid-mobile element systematics of Izu-Bonin volcanic arc lavas show evidence for inputs of two unique slab components with markedly different fluid-mobile element enrichments, the Izu-Bonin boninites can best be explained as simple mixtures of very depleted mantle and a single slab phase with high abundances of fluid-mobile species, along with elevated K, Ba, and other common subduction indicator species. Volcanic arc lavas globally show evidence for a fluid-mobile element enriched component that appears to be similar to serpentinite. Serpentinites generally show marked enrichments in B, As, and Cs, but lesser enrichments in Pb, Li and other alkaline species (e.g., Savov et al 2005; 2007; Deschamps et al 2011). The pattern of relative fluid-mobile species enrichment in the Exp. 352 boninites differs from that of IBM forearc serpentinites, indicating that either serpentinites are not be the source for the enriching fluids, or if they are that the serpentinites are of shallower or deeper origins than those recovered by ODP drilling, which can result in different elemental enrichment patterns (e.g., Mottl et al 2003; Hattori and Guillot 2007).

Sr, Nd, and Pb isotopes of ultramafic xenoliths in volcanic rocks of Eastern China: enriched components EMI and EMII in subcontinental lithosphere

USGS Publications Warehouse

Tatsumoto, M.; Basu, A.R.; Wankang, H.; Junwen, W.; Guanghong, X.

1992-01-01

The UThPb, SmNd, and RbSr isotopic systematics of mafic and ultramafic xenolithic rocks and associated megacrystic inclusions of aluminous augite and garnet, that occur in three alkalic volcanic suites: Kuandian in eastern Liaoning Province, Hanluoba in Hebei Province, and Minxi in western Fujian Province, China are described. In various isotopic data plots, the inclusion data invariably fall outside the isotopic ranges displayed by the host volcanic rocks, testifying to the true xenolithic nature of the inclusions. The major element partitioning data on Ca, Mg, Fe, and Al among the coexisting silicate minerals of the xenoliths establish their growth at ambient mantle temperatures of 1000-1100??C and possible depths of 70-80 km in the subcontinental lithosphere. Although the partitioning of these elements reflects equilibrium between coexisting minerals, equilibria of the Pb, Nd, and Sr isotopic systems among the minerals were not preserved. The disequilibria are most notable with respect to the 206Pb 204Pb ratios of the minerals. On a NdSr isotopic diagram, the inclusion data plot in a wider area than that for oceanic basalts from a distinctly more depleted component than MORB with higher 143Nd 144Nd and a much broader range of 87Sr 86Sr values, paralleling the theoretical trajectory of a sea-water altered lithosphere in NdSr space. The garnets consistently show lower ?? and ?? values than the pyroxenes and pyroxenites, whereas a phlogopite shows the highest ?? and ?? values among all the minerals and rocks studied. In a plot of ??207 and ??208, the host basalts for all three areas show lower ??207 and higher ??208 values than do the xenoliths, indicating derivation of basalts from Th-rich (relative to U) sources and xenoliths from U-rich sources. The xenolith data trends toward the enriched mantle components, EMI and EMII-like, characterized by high 87Sr 86Sr and ??207 values but with slightly higher 143Nd 144Nd. The EMI trend is shown more distinctly by the host basalts. The EMII mantle domain may be present in the Chinese continental lithosphere just above the EMI domain of the basalt source at the lower part of the lithosphere. We argue that the ancient depleted continental lithosphere was metasomatized, imparting the EMI signature, in earlier times ( > 1000 m.y.), and U migrated upward, resulting in high Th U ratios in the lower portion of the lithosphere. Observed high Th U, Rb Sr, 87Sr 86Sr and ??208, low Sm Nd ratios, and a large negative ??Nd in phlogopite pyroxenite with a depleted mantle model age of 2.9 Ga, support our contention that metasomatized continental lower mantle lithosphere is the source for the EMI component. We also suggest that the EMII signature may have been introduced later (less than ??? 500 Ma) by another metasomatic event during the subduction of an oceanic plate, which was partially responsible for some of the observed inter-mineral isotopic disequilibria. ?? 1992.

Evidence from mantle xenoliths for lithosphere removal beneath the central Rio Grande Rift

NASA Astrophysics Data System (ADS)

Byerly, Benjamin L.; Lassiter, John C.

2012-11-01

Seismic tomography beneath the Central Rio Grande Rift (RGR) at ˜34°N shows a low P and S wave velocity zone in the mantle that extends up the base of the Moho. This low-velocity region has been interpreted by (Gao et al., 2004) to be the result of convective removal of a portion of the once >100 km thick Proterozoic lithosphere. The amount of extension in the central RGR is thought to be low (˜25%) and thus cannot account for the amount of lithosphere thinning suggested by seismic tomography. We measured whole rock and mineral major element, trace element, and isotopic compositions of spinel-peridotite xenoliths erupted along the central axis of the rift (Elephant Butte) and the eastern margin of the Colorado Plateau (Cerro Chato) to determine their depth of origin and mantle provenance and to test the delamination hypothesis. If lithosphere removal has not occurred and the low P and S wave velocities are instead the result of hydration or melt infiltration in the lithosphere, then xenoliths erupted on the rift axis should have geochemical compositions similar to Proterozoic sub-continental lithospheric mantle (SCLM). At Cerro Chato, on the margin of the Colorado Plateau, xenoliths were derived from ˜60 km depth and have geochemical signatures similar to Proterozoic sub-continental lithospheric mantle (e.g. refractory major element compositions, LREE-enrichment, enriched Sr and Nd isotopes, unradiogenic Os isotopes). At Elephant Butte, along the central rift axis, two distinct groups of xenoliths are present. The majority of xenoliths from Elephant Butte are LREE-depleted and have fertile major element compositions. Additionally, these xenoliths have isotopic signatures similar to the range for DMM (e.g. 87Sr/86Sr ranging from 0.7018 to 0.7023, ɛNd ranging from 7 to 21, and 187Os/188Os ranging from 0.122 to 0.130). We interpret this group of xenoliths to be derived from asthenospheric mantle. A less-abundant group of xenoliths at Elephant Butte are LREE enriched, have refractory major element compositions, enriched Sr, Nd, and Pb isotopes, and unradiogenic Os isotopes. These are characteristic of Proterozoic SCLM. Both groups of xenoliths from Elephant Butte are derived from ˜45 km depth. We interpret the suite of xenoliths at Elephant Butte to have sampled what was recently the base of the Proterozoic SCLM. We conclude that a portion of the mantle lithosphere has been removed which allowed modern convecting mantle (DMM) to be emplaced at the base of the pre-existing SCLM.

Evolution of the lithospheric mantle beneath Mt. Baekdu (Changbaishan)

NASA Astrophysics Data System (ADS)

Choi, S. H.; Park, K.; Cho, M.; Lee, D. C.

2017-12-01

Major and trace element compositions of minerals as well as Sr-Nd-Hf isotopic compositions of clinopyroxenes from spinel peridotite xenoliths entrained in Late Cenozoic trachybasalt from Mt. Baekdu (Changbaishan) were used to elucidate lithospheric mantle formation and evolution in the eastern North China Craton (NCC). The analyzed peridotites were mainly spinel lherzolites with rare harzburgites. They consisted of olivine, enstatite, diopside and spinel. Plots of the Cr# in spinel against the Mg# in coexisting olivine or spinel suggested an affinity with abyssal peridotites. Comparisons of Cr# and TiO2 in spinel were also compatible with an abyssal peridotite-like composition; however, harzburgites were slightly enriched in TiO2 because of the reaction with MORB-like melt. Temperatures estimated using two-pyroxene thermometry ranged from 750 to 1,010°C, reflecting their lithospheric mantle origin. The REE patterns in clinopyroxenes of the peridotites varied from LREE-depleted to spoon shaped to LREE-enriched, reflecting secondary overprinting effects of metasomatic melts or fluids on the residues from primordial melting. The calculated trace element pattern of metasomatic melt equilibrated with clinopyroxene in Mt. Baekdu peridotite showed strong enrichment in LILEs, Th and U together with slight fractionation in HREEs and considerable depletion in Nb and Ti. The Sr-Nd-Hf isotopic compositions of clinopyroxenes separated from the peridotites varied from more depleted than present-day MORB to bulk Earth values. However, some clinopyroxene showed a decoupling between Nd and Sr isotopes, deviating from the mantle array with a high 87Sr/86Sr ratio. This sample also showed a significant Nd-Hf isotope decoupling lying well above the mantle array. The Lu-Hf and Sm-Nd model ages of residual clinopyroxenes yielded Early Proterozoic to Phanerozoic ages. No signature of Archean cratonic mantle was present. Therefore, Mt. Baekdu peridotite is residual lithospheric mantle that has undergone variable degrees of diachronous melt extraction and infiltration metasomatism involving subduction-related, fluid-bearing silicate melts. The predominance of Phanerozoic Hf model ages indicates that the lherzolites represent lithospheric mantle fragments newly accreted underneath the eastern NCC.

Isotopic and trace element constraints on the petrogenesis of lavas from the Mount Adams volcanic field, Washington

USGS Publications Warehouse

Jicha, B.R.; Hart, G.L.; Johnson, C.M.; Hildreth, Wes; Beard, B.L.; Shirey, S.B.; Valley, J.W.

2009-01-01

Strontium, Nd, Pb, Hf, Os, and O isotope compositions for 30 Quaternary lava flows from the Mount Adams stratovolcano and its basaltic periphery in the Cascade arc, southern Washington, USA indicate a major component from intraplate mantle sources, a relatively small subduction component, and interaction with young mafic crust at depth. Major- and trace-element patterns for Mount Adams lavas are distinct from the rear-arc Simcoe volcanic field and other nearby volcanic centers in the Cascade arc such as Mount St. Helens. Radiogenic isotope (Sr, Nd, Pb, and Hf) compositions do not correlate with geochemical indicators of slab-fluids such as (Sr/P)n and Ba/Nb. Mass-balance modeling calculations, coupled with trace-element and isotopic data, indicate that although the mantle source for the calc-alkaline Adams basalts has been modified with a fluid derived from subducted sediment, the extent of modification is significantly less than what is documented in the southern Cascades. The isotopic and trace-element compositions of most Mount Adams lavas require the presence of enriched and depleted mantle sources, and based on volume-weighted chemical and isotopic compositions for Mount Adams lavas through time, an intraplate mantle source contributed the major magmatic mass of the system. Generation of basaltic andesites to dacites at Mount Adams occurred by assimilation and fractional crystallization in the lower crust, but wholesale crustal melting did not occur. Most lavas have Tb/Yb ratios that are significantly higher than those of MORB, which is consistent with partial melting of the mantle in the presence of residual garnet. ??18O values for olivine phenocrysts in Mount Adams lavas are within the range of typical upper mantle peridotites, precluding involvement of upper crustal sedimentary material or accreted terrane during magma ascent. The restricted Nd and Hf isotope compositions of Mount Adams lavas indicate that these isotope systems are insensitive to crustal interaction in this juvenile arc, in stark contrast to Os isotopes, which are highly sensitive to interaction with young, mafic material in the lower crust. ?? Springer-Verlag 2008.

Decreasing µ142Nd Variation in the Archean Convecting Mantle from 4.0 to 2.5 Ga: Heterogeneous Domain Mixing or Crustal Recycling?

NASA Astrophysics Data System (ADS)

Brandon, A. D.; Debaille, V.

2014-12-01

The 146Sm-142Nd (t1/2=68 Ma) chronometer can be used to examine silicate differentiation in the first 400 Ma of Earth history. Early fractionation between Sm and Nd is recorded in cratonic Archean rocks in their 142Nd/144Nd ratios that that deviate up to ±20 ppm, or μ142Nd - ppm deviation relative to the present-day convecting mantle at 0. These values likely record early extraction of incompatible trace element (ITE) enriched material with -μ142Nd, either as crust or late stage residual melt from a magma ocean, and resulting in a complimentary ITE depleted residual mantle with +μ142Nd. If this early-formed ITE-enriched material was re-incorporated rapidly back into the convecting mantle, both ITE-enriched and ITE-depleted mantle domains would have been established in the Hadean. Alternatively, if it was early-formed crust that remained stable it could have slowly eroded and progressively remixed into the convecting mantle as subducted sediment during the Archean. Each of these scenarios could potentially explain the decrease in the maximum variation in µ142Nd from ±20 at 4.0 Ga to 0 at 2.5 Ga [1,2,3]. In the scenario where these variations reflect mixing of mantle domains, this implies long mantle mixing times of greater than 1 Ga in the Archean in order to preserve the early-formed heterogeneities. This can be achieved in a stagnant lid tectonic regime in the Archean with sporadic and short subduction cycles [2]. This scenario would also indicate that mixing times in the convecting mantle were much slower than the previously proposed 100 Ma in the Hadean and Archean. In the alternative scenario, sediment with -µ142Nd was progressively mixed into the mantle via subduction in the Archean [3]. This scenario doesn't require slow mantle mixing times or a stagnant-lid regime. It requires crustal resident times of up to 750 Ma to maintain a steady supply of ancient sediment recycling over the Archean. Each of these scenarios evoke very contrasting conditions for early Earth history and additional examination is needed. We will consider the geochemical consequences of crustal sediment subduction in order to test the hypothesis of crustal recycling as well as provide additional evidence to aid in resolving this issue. [1] Bennett et al., Science, 318 (2007), p.1907 [2] Debaille et al., EPSL, 373 (2013), p.83 [3] Roth et al., G3, 2014

Cu refertilization of abyssal harzburgites by melt percolation

NASA Astrophysics Data System (ADS)

Ciazela, Jakub; Dick, Henry; Koepke, Juergen; Botcharnikov, Roman; Muszynski, Andrzej; Kuhn, Thomas

2015-04-01

Primitive mantle is depleted in many elements by partial melting processes, but it can be subsequently refertilized by impregnation with percolating melts. It is known that Cu can be enriched in primitive melts, depleting mantle residue, due to the former process (Patten et al. 2013). However, the behavior of Cu in the processes of mantle-melt interaction is poorly understood. The only comprehensive study is based on compositions of orogenic peridotites, representing the subcontinental mantle (Lorand et al. 1993; 2013), where a moderate enrichment of the mantle in Cu (up to ~50 ppm) has been observed. Here, we present the first results obtained for a suite of rocks from an oceanic core complex (OCC), the Kane Megamullion at 22°30'N at the Mid-Atlantic Ridge (Dick et al. 2008). OCC's provide large exposures of mantle and lower crustal rocks on the seafloor on detachment fault footwalls at slow and ultraslow spreading ridges. The mantle rocks are composed of spinel and plagioclase harzburgites. The spinel harzburgites represent depleted mantle, whereas the plagioclase harzburgites were formed by subsequent late-stage melt impregnation in the depleted mantle (Dick et al. 2010). We have determined Cu concentrations in 22 residual spinel harzburgites and 4 plagioclase harzburgites using total digestion ICP-MS. The average Cu concentration in spinel harzburgites is 35±11 ppm Cu (2σ). The average Cu concentration obtained for plagioclase harzburgites is 131±33 ppm Cu (2σ). Additionally, we have analyzed one 1.5 cm thick contact zone between an oxide gabbro vein and residual peridotite. The contact zone, which has been heavily impregnated by the melt, contains 284 ppm Cu. In contrast, the neighboring oxide gabbro vein and the hosting peridotite contain 147 and 68 ppm Cu, respectively. Furthermore, we have determined the concentration of Cu in a dunite (118 ppm), formed in a reaction between the mantle and melt ascending through the lithosphere (Dick et al. 2010). Magmatic processes in the rocks coming from OCCs can be obscured by deformation and alteration. Plastically deformed rocks are common in the damaged zone related to the detachment fault. Metaperidotites from these zones, which show protomylonitic to ultramylonitic textures, are systematically depleted in Cu (15±5 ppm, 2σ) in comparison to non-deformed spinel harzburgites. We have not included the values obtained from non-deformed harzburgites in the calculation of the averages presented above. Thus, the effect of deformation processes does not influence our results. The relatively narrow 0.95 confidence intervals of the means obtained for non-deformed spinel and plagioclase harzburgite species and a large difference between the two means indicate a relatively low influence of alteration. Therefore, we believe the significant enrichment in Cu exhibited by the refertilized mantle rocks is caused exclusively by mantle impregnation with late-stage melts. Enhanced Cu concentrations indicate that the scale of this enrichment can be significantly underestimated in previous studies (Lorand et al. 2013). Dick, H.J.B., Tivey, M.A. & Tucholke, B.E., 2008. Plutonic foundation of a slow-spreading ridge segment: Oceanic core complex at Kane Megamullion, 23°30'N, 45°20'W. Geochemistry, Geophysics, Geosystems 9, Q05014. Dick, H.J.B., Lissenberg, C.J., & Warren, J.M., 2010. Mantle melting, melt transport, and delivery beneath a slow-spreading ridge: The paleo-MAR from 23°15'N to 23°45'N. Journal of Petrology 51, 425-467. Lorand, J.P., Keays, R.R. & Bodinier, J.L., 1993. Copper and noble metal enrichments across the lithosphere-astenosphere boundary of mantle diapirs: evidence from the Lanzo Lherzolite Massif. Journal of Petrology 34, 1111-1140. Lorand, J.P., Luguet, A. & Alard, O., 2013. Platinum-group element systematics and petrogenetics processing of the upper mantle: A review. Lithos 164-167, 2-21. Patten, C., Barnes, S.-J., Mathez, E.A. & Jenner, F.E., 2013. Partition coefficients of chalcophile elements between sulfide and silicate melts and the early crystallization history of sulfide liquid: LA-ICP-MS analysis of MORB sulfide droplets. Chemical Geology 358, 170-188.

Persistence of fertile and hydrous lithospheric mantle beneath the northwestern Ethiopian plateau: Evidence from modal, trace element and Sr-Nd-Hf isotopic compositions of amphibole-bearing mantle xenoliths

NASA Astrophysics Data System (ADS)

Alemayehu, Melesse; Zhang, Hong-Fu; Aulbach, Sonja

2017-07-01

We present new trace element compositions of amphiboles, Sr-Nd-Hf isotope compositions of clinopyroxenes and mineral modes for spinel peridotite xenoliths that were entrained in a Miocene alkali basalt (Gundeweyn, northwestern Ethiopian plateau), in order to understand the geochemical evolution and variation occurring within the continental lithospheric mantle (CLM) in close proximity to the East African Rift system, and its dynamic implications. With the exception of a single amphibole-bearing sample that is depleted in LREE (La/YbN = 0.45 × Cl), amphiboles in lherzolites and in one harzburgite show variable degrees of LREE enrichment (La/YbN = 2.5-12.1 × Cl) with flat HREE (Dy/YbN = 1.5-2.1 × Cl). Lherzolitic clinoyroxenes have 87Sr/86Sr (0.70227 to 0.70357), 143Nd/144Nd (0.51285 to 0.51346), and 176Hf/177Hf (0.28297 to 0.28360) ranging between depleted lithosphere and enriched mantle. LREE-enriched clinopyroxenes generally have more enriched isotope compositions than depleted ones. While lherzolites with isotope compositions similar to those of the Afar plume result from the most recent metasomatic overprint, isotope compositions more depleted than present-day MORB can be explained by an older melt extraction and/or isotopic rehomogenisation event, possibly related to the Pan-African orogeny. Several generations of amphibole are recognized in accord with this multi-stage evolution. Texturally unequilibrated amphibole occurring within the peridotite matrix and in melt pockets attest to continued hydration and refertilization of the lithospheric mantle subsequent to Oligocene flood basalt magmatism, during which an earlier-emplaced inventory of amphibole was likely largely consumed. However, a single harzburgite contains amphibole with the highest Mg# and lowest TiO2 content, which is interpreted as sampling a volumetrically subordinate mantle region beneath the Ethiopian plateau that was not tapped during flood basalt magmatism. Strikingly, both trace-element enriched and depleted lherzolites have high clinopyroxene and orthopyroxene and low olivine contents (median 15, 24 and 56 vol.%), combined with primitive olivine Mg# (median 89.5), indicating the presence of refertilized mantle beneath Gundeweyn. Despite its fertility and FeO-rich character (hence high inferred density), and impingement by the Afar plume, the CLM beneath the Ethiopian plateau, though apparently thinned through thermochemical erosion, has so far resisted whole-sale delamination or dripping. This is tentatively ascribed to insufficient stress and density contrasts at the periphery of the Afar plume, which reached its greatest thermochemical buoyancy in the Afar region, northeast of Gundeweyn.

Constraints From the Rock Record, and Complementary Speculation, on Subduction and the Evolution of the Mantle

NASA Astrophysics Data System (ADS)

Kelemen, P.

2006-12-01

As time permits, I will cover some of the following: (1) What crustal components are subducted for long term recycling? (a) Revisiting an old approach, relatively new constraints on the "subduction component" in arc magmas can be derived from comparison of primitive MORB with a compilation of primitive arc lavas (Kelemen et al., ToG 03). These provide quantitative estimates for the composition of the "arc residue" in subducting oceanic crust and sediment. (b) It may be that substantial recycling in subduction settings is from the hanging wall, via subdution erosion (von Huene & Scholl, Rev Geophys 91) and "delamination" (Herzberg et al CMP 83; Kay & Kay GCA 88; Arndt & Goldstein T'phys 89). (c) Subducting sediment may migrate into the mantle wedge via buoyancy (Kelemen et al., ToG 03; Gerya & Yuen EPSL 03). (d) New ICPMS data are available on trace element characteristics of arc (Kelemen et al., ToG 03; Greene et al J Pet 06) and oceanic lower crust (not published, sorry!). I will illustrate evolution of radiogenic parent-daughter ratios as constrained by these data. (2) Where do residual peridotites go during subduction? I see three interesting possibilities. (a) Highly depleted cratonic mantle peridotites formed as relatively shallow residues (Bernstein et al EPSL 98), were carried to greater depth to form metamorphic garnet (Kelemen et al EPSL 98), and then were imbricated or rose buoyantly to become a long-lasting part of the cratonic mantle (Oxburgh & Parmentier, JGSL 77), where they have been affected by Arc(hean) processes (Kelemen et al EPSL 98). High light REE contents as well as measured high H2O in cratonic mantle indicate that it is not dry and viscous, so its long term stability is not well understood. There is insufficient work on how compositional buoyancy of highly depleted residues affects cratonic mantle stability. (b) Perhaps some cold, dry residues remain for long periods in the lower mantle. Trace element data suggest that some ubiquitous process igneous or metamorphic enriches ridge and ophiolite peridotites in Pb relative to U and Th (Godard et al Eos 05). Sequestration of such a low U/Pb and Th/Pb component could help explain global Pb isotope systematics. (c) Some residual peridotites recirculate in the mantle washing machine, emerging as depleted peridotites on the seafloor with little igneous crust. (3) What is the fate of partial melts of subducted basaltic eclogite, when they react with mantle peridotite above subduction zones and beneath ocean islands? Variable time scales, permeability and melt viscosity suggest three possible scenarios: (a) much eclogite melt is trapped within a carapace of pyroxenite, and hydrofracture extracts this melt; (b) eclogite melt reacts to form solid pyroxenite, which then re-melts (Sobolev et al Nature 04); (c) eclogite melt reacts to form pyroxene-rich peridotite plus modified melt in equilibrium with olivine (Kelemen et al EPSL 98).

Collision-induced post-plateau volcanism: Evidence from a seamount on Ontong Java Plateau

NASA Astrophysics Data System (ADS)

Hanyu, Takeshi; Tejada, Maria Luisa G.; Shimizu, Kenji; Ishizuka, Osamu; Fujii, Toshiyuki; Kimura, Jun-Ichi; Chang, Qing; Senda, Ryoko; Miyazaki, Takashi; Hirahara, Yuka; Vaglarov, Bogdan S.; Goto, Kosuke T.; Ishikawa, Akira

2017-12-01

Many seamounts on the Ontong Java Plateau (OJP) occur near the Stewart Arch, a topographic high that extends parallel to the North Solomon Trench along the southern margins of the plateau. Despite the thick sediment cover, several volcanic cones with strong acoustic reflection were discovered on the submarine flank of the Nuugurigia Seamount. From such volcanic cones, basalts were successfully sampled by dredging. Radiometric dating of basalts and ferromanganese encrustation indicate eruption age of 20-25 Ma, significantly younger than the 122 Ma main OJP plateau and post-plateau basalts. The age range coincides with the collision of the OJP with the Solomon Arc. The Nuugurigia basalts geochemically differ from any other rocks sampled on the OJP so far. They are alkali basalts with elevated Sr, low Zr and Hf, and Enriched Mantle-I (EMI)-like isotopic composition. Parental magmas of these alkali basalts may have formed by small-degree melting of peridotitic mantle impregnated with recycled pyroxenite material having enriched geochemical composition in the OJP's mantle root. We conclude that small-volume alkali basalts from the enriched mantle root migrated through faults or fractures caused by the collision along the Stewart Arch to form the seamount. Our results suggest that the collision of the OJP with the Solomon arc played an important role in the origin of similar post-plateau seamounts along the Stewart Arch.

Post-collisional alkaline magmatism as gateway for metal and sulfur enrichment of the continental lower crust

NASA Astrophysics Data System (ADS)

Fiorentini, Marco L.; LaFlamme, Crystal; Denyszyn, Steven; Mole, David; Maas, Roland; Locmelis, Marek; Caruso, Stefano; Bui, Thi-Hao

2018-02-01

Mafic and ultramafic magmas that intrude into the lower crust can preserve evidence for metal and sulfur transfer from the lithospheric mantle into the lower continental crust. Here we focus on a series of ultramafic, alkaline pipes in the Ivrea Zone (NW Italy), which exposes deeply buried (6-11 kbar), migmatitic metasedimentary rocks intruded by voluminous basaltic magmas of the Mafic Complex, a major crustal underplating event precisely dated via U/Pb CA-IDTIMS on zircon at 286.8 ± 0.4 Ma. The ultramafic pipes postdate the Mafic Complex and from 100 to 300 m wide cumulate-rich conduits. They are hydrated and carbonated, have unusually high incompatible element concentrations and contain blebby and semi-massive Ni-Cu-PGE sulfide mineralisation. The sulfides occur as coarse intergranular nodules (>10 mm) and as small intragranular blebs (<1 mm) hosted in olivine, and have homogeneous, mantle-like δ34S (+1.35 ± 0.25‰). This homogeneity suggests that the pipes reached sulfide supersaturation without addition of crustal sulfur, and that the δ34S signature is representative of the continental lithospheric mantle. One of the pipes, the 249 Ma Valmaggia pipe, carries a very distinctive Sr-Nd-Hf-Pb isotopic composition in its core (87Sr/86Sr 0.70250, εNd-18, εHf-18, 206Pb/204Pb 16.0, 207Pb/204Pb 15.16, 208Pb/204Pb 35.87), very different from the margin of this pipe and from other pipes that have higher 87Sr/86Sr, εNd and 206Pb/204Pb. The unusual isotopic composition of the Valmaggia pipe requires a source with long-term (2500-1500 million years) U-, Th- and Rb-depletion and LREE enrichment. Such compositions are found in Late Archean/Early Proterozoic granulites and lower crustal xenoliths. We suggest that the unusual isotopic composition of the Valmaggia pipe reflects contamination of the mantle source of the pipe with a crustal component that is neither represented in the local Paleozoic crust nor in the isotopically anomalous hydrated mantle inferred as the source of the large-volume mafic underplate that formed the Mafic Complex. During post-collisional gravitational collapse of the Variscan Orogen, this source produced the alkaline, metal (Ni, Cu, PGE)- and volatile (H2O, CO2, S)-rich mafic-ultramafic magma that formed the deep-crustal intrusion at Valmaggia. U/Pb dating of other chemically and geologically comparable pipes in the area shows that this process was active over at least 40 Ma. The Ivrea pipes illustrate how the lower continental crust can be fertilised with mantle-derived metals and volatiles, which are available for later remobilisation into upper-crustal ore systems. World-class mineral deposits along the margins of lithospheric blocks may thus be the result of both favourable crustal architecture (focussing of magmas and fluids) and localised volatile and metal enrichment of the lower crust related to mantle-derived hydrous metasomatism.

Devonian alkaline magmatic belt along the northern margin of the North China Block: Petrogenesis and tectonic implications

NASA Astrophysics Data System (ADS)

Zhang, Qi-Qi; Zhang, Shuan-Hong; Zhao, Yue; Liu, Jian-Min

2018-03-01

Some Devonian magmatic rocks have been identified from the northern margin of the North China Block (NCB) in recent years. However, their petrogenesis and tectonic setting are still highly controversial. Here we present new geochronological, Sr-Nd-Hf isotopic and whole-rock chemical data on several newly identified and previously reported Devonian alkaline complexes, including mafic-ultramafic rocks (pyroxenites and gabbros), alkaline rocks (syenites, monzonites) and alkaline granites in the northern NCB. We firstly identified some mafic-ultramafic rocks coeval with monzonite and quartz monzonite in the Sandaogou and Wulanhada alkaline intrusions. New zircon U-Pb dating of 16 samples from the Baicaigou, Gaojiacun, Sandaogou, Wulanhada and Chifeng alkaline intrusions combined with previous geochronological results indicate that the Devonian alkaline rocks emplaced during the early-middle Devonian at around 400-380 Ma and constitute an E-W-trending alkaline magmatic belt that extend ca. 900 km long along the northern margin of the NCB. Whole-rock geochemical and Sr-Nd-Hf isotopic data reveal that the Devonian alkaline rocks were mainly originated from partial melting of a variably enriched lithospheric mantle with different involvement of ancient lower crustal component and fractional crystallization. The Devonian alkaline magmatic belt rocks in the northern NCB are characterized by very weak or no deformations and were most likely related to post-collision extension after arc-continent collision between the Bainaimiao island arc and the northern margin of North China Craton during the latest Silurian. Partial melting of subcontinental lithospheric mantle to produce the Devonian alkaline magmatic rocks suggests that the northern North China Craton has an inhomogeneous, variably enriched subcontinental lithospheric mantle and was characterized by significant vertical crustal growth during the Devonian period.

Atmospheric noble gases in Mid-Ocean Ridge Basalts: Identification of atmospheric contamination processes

NASA Astrophysics Data System (ADS)

Roubinet, Claire; Moreira, Manuel A.

2018-02-01

Noble gases in oceanic basalts always show the presence in variable proportions of a component having elemental and isotopic compositions that are similar to those of the atmosphere and distinct from the mantle composition. Although this component could be mantle-derived (e.g. subduction of air or seawater-derived noble gases trapped in altered oceanic crust and sediments), it is most often suggested that this air component is added after sample collection and probably during storage at ambient air, although the mechanism remains unknown. In an attempt to reduce this atmospheric component observed in MORBs, four experimental protocols have been followed in this study. These protocols are based on the hypothesis that air can be removed from the samples, as it appears to be sheltered in distinct vesicles compared to those filled with mantle gases. All of the protocols involve a glove box filled with nitrogen, and in certain cases, the samples are stored under primary vacuum (lower than 10-2 mbar) to pump air out or, alternatively, under high pressure of N2 to expel atmospheric noble gases. In all protocols, three components are observed: atmospheric, fractionated atmospheric and magmatic. The fractionated air component seems to be derived from the non-vitreous part of the pillow-lava, which has cooled more slowly. This component is enriched in Ne relative to Ar, reflecting a diffusive process. This contaminant has already been observed in other studies and thus seems to be relatively common. Although it is less visible, unfractionated air has also been detected in some crushing steps, which tends to indicate that despite the experiments, air is still present in the vesicles. This result is surprising, since studies have demonstrated that atmospheric contamination could be limited if samples were stored under nitrogen quickly after their recovery from the seafloor. Thus, the failure of the protocols could be explained by the insufficient duration of these protocols or by the inaccessibility of vesicles filled with air as assessed by (Ballentine and Barfod, 2000).

Seychelles alkaline suite records the culmination of Deccan Traps continental flood volcanism

NASA Astrophysics Data System (ADS)

Owen-Smith, T. M.; Ashwal, L. D.; Torsvik, T. H.; Ganerød, M.; Nebel, O.; Webb, S. J.; Werner, S. C.

2013-12-01

Silhouette and North Islands in the Seychelles represent an alkaline plutonic-volcanic complex, dated at 63 to 63.5 Ma by U-Pb zircon and 40Ar/39Ar methods. This magmatism coincides with the final stages of the cataclysmic Deccan Traps continental flood volcanism in India (67 to 63 Ma), and thus a causal link has been suggested. Recent reconstructions have placed the Seychelles islands adjacent to the Laxmi Ridge and at the western margin of the Réunion mantle plume at the time of formation of the complex. Here we present geochemical evidence in support of the notion that the Seychelles alkaline magmatism was initiated by the peripheral activity of the Réunion mantle plume and is thus part of the Deccan magmatic event. Positive εNd (0.59 to 3.76) and εHf (0.82 to 6.79) and initial Sr of 0.703507 to 0.705643 at 65 Ma indicate derivation of the Seychelles alkaline magmas from a Réunion-like mantle source with an additional minor enriched component, suggesting entrainment of sub-continental lithospheric mantle. The similarity in trace element composition between the Seychelles suite and Deccan alkaline felsic and mafic rocks provides additional evidence for a common mantle source for the Seychelles and Deccan magmatism. Furthermore, we demonstrate the role of fractional crystallisation in the evolution of the alkaline suite. Modelling using major elements suggests that fractional crystallisation and varying degrees of accumulation of olivine, plagioclase, ilmenite, clinopyroxene, alkali feldspar and apatite can describe the spectrum of rock types, from gabbro, through syenite, to granite.

Sr isotopic composition of Afar volcanics and its implication for mantle evolution

NASA Astrophysics Data System (ADS)

Barberi, F.; Civetta, L.; Varet, J.

1980-10-01

Investigations of Rb-Sr systematics of basalts from the Afar depression (Ethiopia) indicate the presence of a heterogeneous mantle source region. The Sr isotopic compositions of the basalts from the Afar axial and transverse ranges identify source regions which are enriched in LIL elements and radiogenic Sr (axial ranges) and others which are relatively depleted (transverse ranges). Sr isotopic composition of basalts from the Red Sea, Gulf of Aden and Gulf of Tadjoura, which range from 0.70300 to 0.70340 are also reported and compared with the more radiogenic Afar region, which is characterized by 87Sr/ 86Sr ranging from 0.70328 to 0.70410. Available geochemical and isotopic data suggest that a relation exists between magma composition and the advancement of the rifting process through progressive lithosphere attenuation leading to continental break-up. However, the petrogenetic process is not simple and probably implies a vertically zoned mantle beneath the Afar region. Sr isotopic evidence suggests that the vertically zoned mantle is more radiogenic and enriched in LIL elements in its upper part.

Silurian/Ordovician asymmetrical sill-like bodies from La Codosera syncline, W Spain: A case of tholeiitic partial melts emplaced in a single magma pulse and derived from a metasomatized mantle source

NASA Astrophysics Data System (ADS)

López-Moro, F. J.; Murciego, A.; López-Plaza, M.

2007-07-01

A Silurian/Ordovician extensional event in the southernmost sectors of the Central Iberian Zone is inferred from the Sm/Nd isochron obtained (436 ± 17 Ma) after the diabase sills from the La Codosera syncline. From the geochemical and mineralogical points of view, the diabase sills are subalkaline and range between high-Mg tholeiite diabases to tholeiite andesites. LREE enrichment, an Nb negative anomaly, the absence of a Ta trough and a high Nd isotope signature ( ɛNd t = + 6) are the most relevant geochemical features. The diabase bodies are up to 330 m in thickness and were sampled from bottom to top along several different sections, permitting the definition of an accumulation of clinopyroxene, olivine and plagioclase close to chilled margins at the bottom, and abundant pegmatoid layers at the top. Chemical profiles and mass-balance modelling suggest that the bulk rock and chilled margin compositions are not dissimilar, defining an unusual S-type vertical compositional profile for large (> 50 m thick) sills, which in turn strongly suggests a single magma pulse and a probable gravitational settling. Assuming chilled margin samples as the parental magma, as well as Cr-enriched samples as cumulate layers, a two-stage liquid line of descent has been established, the first one consisting of a clinopyroxene-plagioclase-olivine cumulate assemblage. A second stage in relation to the depletion in Ti, Fe and V is accounted for by ilmenite fractionation, along with that of clinopyroxene, plagioclase and olivine fractionation. Thermobarometric estimations reveal that the clinopyroxene (around 1100 °C and 197 MPa) was a late mineral phase, whereas the plagioclase (around 1200 °C) was pre- to syn-emplacement, in agreement with the presence only of plagioclase phenocrysts in the chilled margins and the very abundant positive Eu anomaly. The energy constraint modelling is consistent with the lack of a significant assimilation process owing to the high temperature contrast between the country rock and the magma itself. The compositional characteristics of chilled margins enable them to be ruled out as primary melts in equilibrium with mantle olivine (Fo 91), a certain amount of olivine fractionation being required, which might have occurred in magma conduits en route to shallow emplacement levels in the crust. Spinel lherzolitic xenoliths from the European Cenozoic alkaline magmatism appear to be unsuitable protoliths to account for the chilled margin compositions. Instead, a hybrid mantle source consisting of a small amount of OIB-mantle component (5 wt.%) and a depleted end-member mantle component seems to be a plausible protolith, resulting in a good fit with the fractionation-corrected chilled margin trends for 10% of partial melting.

Silicon and Zinc Isotopes in Ocean Island Basalts

NASA Astrophysics Data System (ADS)

Pringle, E. A.; Savage, P. S.; Jackson, M. G.; Moreira, M. A.; Day, J. M.; Moynier, F.

2013-12-01

Analyses of Ocean Island Basalts (OIB) have shown that the Earth's mantle contains isotopically distinct components, but current debate about the degree and scale of compositional variability persists. Isotopic heterogeneities in OIB for both radiogenic (e.g. Sr, Nd, Pb) and stable (e.g. Li, O, Ca) isotope systems have been attributed to the presence of recycled materials in different mantle reservoirs [1]. The study of both silicon and zinc isotopes in OIB form a complimentary approach to investigate potential heterogeneities in the mantle. Both isotope systems show limited fractionation during igneous process [2,3]. However, both Si and Zn exhibit larger (>1‰) variability in low-temperature environments (e.g. as a result of chemical weathering and biological utilization). Therefore, Si and Zn isotopes may be useful as tracers for the presence of crustal material (derived from low-T surface processes) in OIB source regions. Furthermore, characterizing the isotopic composition of the mantle is of central importance to the use of these isotopic systems as a basis for interplanetary comparisons. Here we present high-precision Si and Zn isotopic data obtained by MC-ICPMS for a diverse suite of OIB representing the EM-1, EM-2, and HIMU mantle components. Samples represent locations in the Pacific, Atlantic, and Indian Oceans. Data are reported as the permil deviation (×2 sd) from NBS28 for Si (δ30Si) and JMC-Lyon for Zn (δ66Zn). Average δ30Si values for OIB from EM-1 (-0.32×0.09‰), EM-2 (-0.30×0.03‰), and HIMU (-0.34×0.12‰) are all in general agreement with previous estimates for the δ30Si value of Bulk Silicate Earth (BSE) [4]. Similarly, the δ66Zn average values for OIB from the EM-1, EM-2, and HIMU components (0.31×0.06‰, 0.31×0.04‰, 0.31×0.05‰, respectively) agree well with previously published data for the δ66Zn value of BSE [3]. At the current levels of precision, both Si and Zn isotopes exhibit little variation in OIB, confirming the large-scale homogeneity of the mantle for these isotopic systems. Furthermore, when averaged according to surface location, neither Si nor Zn shows any variation in isotopic composition according to oceanic basin. However, some small variations in the data may be present; many HIMU samples (Mangaia, Cape Verde) are enriched in the lighter isotopes of Si (δ30Si tending toward chondritic values), which might reflect preservation of isotopic heterogeneity within the mantle, an incorporation of an isotopically light component in the source of these lavas, or isotopic fractionation during magmatic differentiation. References: [1] Hofmann, RiMG 2007 [2] Savage et al., GCA 2011 [3] Chen et al., EPSL 2013 [4] Savage et al., EPSL 2010

Composition of the lithospheric mantle in the northern part of Siberian craton: Constraints from peridotites in the Obnazhennaya kimberlite

NASA Astrophysics Data System (ADS)

Sun, Jing; Liu, Chuan-Zhou; Kostrovisky, Sergey I.; Wu, Fu-Yuan; Yang, Jin-Hui; Chu, Zhu-Yin; Yang, Yue-Heng; Kalashnikova, Tatiana; Fan, Sheng

2017-12-01

The character of the lithospheric mantle of the northern Siberian craton is not well established; nearly all published data are for mantle xenoliths from a single kimberlite in the center of the craton (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma) in the northern part of Siberian craton. The Obnazhennaya mantle xenoliths include spinel harzburgites, spinel dunites, spinel lherzolites and spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt% Al2O3, 0.41-3.11 wt% CaO and 0.00-0.09 wt% TiO2, whereas the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt% Al2O3, 2.91-7.55 wt% CaO and 0.04-0.15 wt% TiO2. The trace element compositions and mineralogical textures of the Obnazhennaya xenoliths indicate the occurrence of metasomatic enrichments, including carbonatite melts, basaltic melts from Siberian Trap and kimberlitic melts. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, both spinel and spinel-garnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. But the higher Al2O3 and Os character of these lherzolites suggest that they were not juvenile mantle but the refertilized ancient mantle. Therefore, our results suggest that the cratonic mantle beneath the northern part of Siberian craton contain both ancient and reworked lithospheric mantle, and the metasomatism may not be effective at overprinting/eroding the pre-existing lithosphere.

The Fine Geochemical Structure of the Hawaiian Mantle Plume: Relation to the Earth's Lowermost Mantle

NASA Astrophysics Data System (ADS)

Weis, D.; Harrison, L.

2017-12-01

The Hawaiian mantle plume has been active for >80 Ma with the highest magmatic flux, also distinctly increasing with time. The identification of two clear geochemical trends (Loa-Kea) among Hawaiian volcanoes in all isotope systems has implications for the dynamics and internal structure of the plume conduit and source in the deep mantle. A compilation of modern isotopic data on Hawaiian shield volcanoes and from the Northwest Hawaiian Ridge (NWHR), focusing specifically on high-precision Pb isotopes integrated with Sr, Nd and Hf isotopes, indicates the presence of source differences for Loa- and Kea-trend volcanoes that are maintained throughout the 1 Ma activity of each volcano. These differences extend back in time on all the Hawaiian Islands ( 5 Ma), and as far back as 47 Ma on the NWHR. In all isotope systems, the Loa-trend basalts are more heterogeneous by a factor of 1.5 than the Kea-trend basalts. The Hawaiian mantle plume overlies the boundary between ambient Pacific lower mantle on the Kea side and the Pacific LLSVP on the Loa side. Geochemical differences between Kea and Loa trends reflect preferential sampling of these two distinct sources of deep mantle material, with additional contribution of ULVZ material sporadically on the Loa side. Plume movement up the gently sloping edge of the LLSVP resulted in entrainment of greater amounts of LLSVP-enriched material over time, and explains why the Hawaiian mantle plume dramatically strengthens over time, contrary to plume models. Similar indications of preferential sampling at the edges of the African LLSVP are found in Kerguelen and Tristan da Cunha basalts in the Indian and Atlantic oceans, respectively. The anomalous low-velocity zones at the core-mantle boundary store geochemical heterogeneities that are enriched in recycled material (EM-I type) with different compositions under the Pacific and under Africa, and that are sampled by strong mantle plumes such as Hawaii and Kerguelen.

Pb, Sr, and Nd isotopic compositions of a suite of Late Archean, igneous rocks, eastern Beartooth Mountains: implications for crust-mantle evolution

USGS Publications Warehouse

Wooden, J.L.; Mueller, P.A.

1988-01-01

A series of compositionally diverse, Late Archean rocks (2.74-2.79 Ga old) from the eastern Beartooth Mountains, Montana and Wyoming, U.S.A., have the same initial Pb, Sr, and Nd isotopic ratios. Lead and Sr initial ratios are higher and Nd initial ratios lower than would be expected for rocks derived from model mantle sources and strongly indicate the involvement of an older crustal reservoir in the genesis of these rocks. Crustal contamination during emplacement can be ruled out for a variety of reasons. Instead a model involving subduction of continental detritus and contamination of the overlying mantle as is often proposed for modern subduction environments is preferred. This contaminated mantle would have all the isotopic characteristics of mantle enriched by internal mantle metasomatism but would require no long-term growth or changes in parent to daughter element ratios. This contaminated mantle would make a good source for some of the Cenozoic mafic volcanics of the Columbia River, Snake River Plain, and Yellowstone volcanic fields that are proposed to come from ancient, enriched lithospheric mantle. The isotopic characteristics of the 2.70 Ga old Stillwater Complex are a perfect match for the proposed contaminated mantle which provides an alternative to crustal contamination during emplacement. The Pb isotopic characteristics of the Late Archean rocks of the eastern Beartooth Mountains are similar to those of other Late Archean rocks of the Wyoming Province and suggest that Early Archean, upper crustal rocks were common in this terrane. The isotopic signatures of Late Archean rocks in the Wyoming Province are distinctive from those of other Archean cratons in North America which are dominated by a MORB-like, Archean mantle source (Superior Province) and/or a long-term depleted crustal source (Greenland). ?? 1988.

Geochemical and NdSr isotopic composition of deep-sea turbidites: Crustal evolution and plate tectonic associations

NASA Astrophysics Data System (ADS)

McLennan, S. M.; Taylor, S. R.; McCulloch, M. T.; Maynard, J. B.

1990-07-01

Petrographic, geochemical, and isotopic data for turbidites from a variety of tectonic settings exhibit considerable variability that is related to tectonic association. Passive margin turbidites (Trailing Edge, Continental Collision) display high framework quartz (Q) content in sands, evolved major element compositions (high Si/Al, K/Na), incompatible element enrichments (high Th/Sc, La/Sc, La/Yb), negative Eu-anomalies and variable Th/U ratios. They have low 143Nd /144Nd and high 87Sr /86Sr ( ɛNd = -26 to -10; 87Sr /86Sr = 0.709 to 0.734 ), indicating a dominance of old upper crustal sources. Active margin settings (Fore Arc, Continental Arc, Back Arc, Strike Slip) commonly exhibit quite different compositions. Th/Sc varies from <0.01 to 1.8, and ɛNd varies from -13.8 to +8.3. Eu-anomalies range from no anomaly ( Eu/Eu ∗ = 1.0 ) to Eu-depletions typical of post-Archean shales ( Eu/Eu ∗ = 0.65 ). Active margin data are explained by mixtures of young arc-derived material, with variable composition and old upper crustal sources. Major element data indicate that passive margin turbidites have experienced more severe weathering histories than those from active settings. Most trace elements are enriched in muds relative to associated sands because of dilution effects from quartz and calcite and concentration of trace elements in clays. Exceptions include Zr, Hf (heavy mineral influence) and Tl (enriched in feldspar) which display enrichments in sands. Active margin sands commonly exhibit higher Eu/Eu ∗ than associated muds, resulting from concentration of plagioclase during sorting. Some associated sands and muds, especially from active settings, have systematic differences in Th/Sc ratios and Nd-isotopic composition, indicating that various provenance components may separate into different grain-size fractions during sedimentary sorting processes. Trace element abundances of modern turbidites, from both active and passive settings, differ from Archean turbidites in several important ways. Modern turbidites have less uniformity, for example, in Th/Sc ratios. On average, modern turbidites have greater depletions in Eu (lower Eu/Eu ∗) than do Archean turbidites, suggesting that the processes of intracrustal differentiation (involving plagioclase fractionation) are of greater importance for crustal evolution at modern continental margins than they were during the Archean. Modern turbidites do not display HREE depletion, a feature commonly seen in Archean data. HREE depletion ( Gd N/Yb N > 2.0 ) in Archean sediments results from incorporation of felsic igneous rocks that were in equilibrium (or their sources were in equilibrium) with garnet sometime in their history. Absence of HREE depletion at modern continental margins suggests that processes of crust formation (or mantle source compositions) may have differed. Differences in trace element abundances for Archean and modern turbidites add support to suggestions that upper continental crust compositions and major processes responsible for continental crust differentiation differed during the Archean. Neodymium model ages, thought to approximate average provenance age, are highly variable ( TDMND = 0-2.6 Ga) in modern turbidites, in contrast with studies that indicate Nd-model ages of lithified Phanerozoic sediment are fairly constant at about 1.5-2.0 Ga. This variability indicates that continental margin sediments incorporate new mantle-derived components, as well as continental crust of widely varying age, during recycling. The apparent dearth of ancient sediments with Nd-model age similar to stratigraphic age supports the suggestion that preservation potential of sediments is related to tectonic setting. Many samples from active settings have isotopic compositions similar to or only slightly evolved from mantle-derived igneous rocks. Subduction of active margin turbidites should be considered in models of crust-mantle recycling. For short-term recycling, such as that postulated for island arc petrogenesis, arc-derived turbidites cannot be easily recognized as a source component because of the lack of time available for isotopic evolution. If turbidites were incorporated into the sources of ocean island volcanics, the isotopic signatures would be considerably more evolved since most models call for long mantle storage times (1.0-2.0 Ga), prior to incorporation. Four provenance components are recognized on the basis of geochemistry and Nd-isotopic composition: (1) Old Upper Continental Crust (old igneous/metamorphic terranes, recycled sediment); (2) Young Undifferentiated Arc (young volcanic/plutonic source that has not experienced plagioclase fractionation); (3) Young Differentiated Arc (young volcanic/plutonic source that has experienced plagioclase fractionation); (4) MORB (minor). Relative proportions of these components are influenced by the plate tectonic association of the provenance and are typically (but not necessarily) reflected in the depositional basin. Provenance of quartzose (mainly passive settings) and non-quartzose (mainly active settings) turbidites can be characterized by bulk composition (e.g., Th/Sc) and Nd-isotopic composition (reflecting age).

Mid Carboniferous lamprophyres, Cobequid Fault Zone, eastern Canada, linked to sodic granites, voluminous gabbro, and albitization

NASA Astrophysics Data System (ADS)

Pe-Piper, Georgia; Piper, David J. W.; Papoutsa, Angeliki

2018-01-01

Major intra-continental shear zones developed during the later stages of continental collision in a back-arc setting are sites of prolonged magmatism. Mantle metasomatism results from both melting of subducted sediments and oceanic crust. In the Cobequid Fault Zone of the northern Appalachians, back-arc A-type granites and gabbros dated ca. 360 Ma are locally intruded by lamprophyric dykes dated ca. 335 Ma. All the lamprophyres are kersantites with biotite and albite, lesser ilmenite, titanite and fluorapatite, and minor magmatic calcite, allanite, pyrite, magnetite, quartz and K-feldspar in some samples. The lamprophyres show enrichment in Rb, Ba, K, Th and REE and classify as calc-alkaline lamprophyre on the basis of biotite and whole rock chemistry. Pb isotopes lie on a mixing line between normal mantle-derived gabbro and OIB magma. Nd isotopes range from 1.3-3.5 εNdt, a little lower than in local gabbro. Most lamprophyres have δ18O = 3.8-4.4‰. Country rock is cut by pyrite-(Mg)-chlorite veins with euhedral allanite crystals that resemble the lamprophyres mineralogically, with the Mg-chlorite representing chloritized glass. Early Carboniferous unenriched mafic dykes and minor volcanic rocks are widespread along the major active strike-slip fault zones. The lamprophyres are geographically restricted to within 10 km of a small granitoid pluton with some sodic amphibole and widespread albitization. This was displaced by early Carboniferous strike-slip faulting from its original position close to the large Wentworth Pluton, the site of mantle-derived sodic amphibole granite, a major late gabbro pluton, and a volcanic carapace several kilometres thick, previously demonstrated to be the site of mantle upwelling and metasomatism. The age of the lamprophyres implies that enriched source material in upper lithospheric mantle or lower crust was displaced 50 km by crustal scale strike-slip faulting after enrichment by the mantle upwelling before lamprophyre emplacement. This indicates a multi-stage process to emplace lamprophyric magma.

Composition of plume-influenced mid-ocean ridge lavas and glasses from the Mid-Atlantic Ridge, East Pacific Rise, Galápagos Spreading Center, and Gulf of Aden

NASA Astrophysics Data System (ADS)

Kelley, Katherine A.; Kingsley, Richard; Schilling, Jean-Guy

2013-01-01

The global mid-ocean ridge system is peppered with localities where mantle plumes impinge on oceanic spreading centers. Here, we present new, high resolution and high precision data for 40 trace elements in 573 samples of variably plume-influenced mid-ocean ridge basalts from the Mid-Atlantic ridge, the Easter Microplate and Salas y Gomez seamounts, the Galápagos spreading center, and the Gulf of Aden, in addition to previously unpublished major element and isotopic data for these regions. Included in the data set are the unconventional trace elements Mo, Cd, Sn, Sb, W, and Tl, which are not commonly reported by most geochemical studies. We show variations in the ratios Mo/Ce, Cd/Dy, Sn/Sm, Sb/Ce, W/U, and Rb/Tl, which are expected not to fractionate significantly during melting or crystallization, as a function of proximity to plume-related features on these ridges. The Cd/Dy and Sn/Sm ratios show little variation with plume proximity, although higher Cd/Dy may signal increases in the role of garnet in the mantle source beneath some plumes. Globally, the Rb/Tl ratio closely approximates the La/SmN ratio, and thus provides a sensitive tracer of enriched mantle domains. The W/U ratio is not elevated at plume centers, but we find significant enrichments in W/U, and to a lesser extent the Mo/Ce and Sb/Ce ratios, at mid-ocean ridges proximal to plumes. Such enrichments may provide evidence of far-field entrainment of lower mantle material that has interacted with the core by deeply-rooted, upwelling mantle plumes.

Osmium Isotope Compositions of Komatiite Sources Through Time

NASA Astrophysics Data System (ADS)

Walker, R. J.

2001-12-01

Extending Os isotopic measurements to ancient plume sources may help to constrain how and when the well-documented isotopic heterogeneities in modern systems were created. Komatiites and picrites associated with plume-related volcanism are valuable tracers of the Os isotopic composition of plumes because of their typically high Os concentrations and relatively low Re/Os. Re-Os data are now available for a variety of Phanerozoic, Proterozoic and Archean komatiites and picrites. As with modern plumes, the sources of Archean and Proterozoic komatiites exhibit a large range of initial 187Os/188Os ratios. Most komatiites are dominated by sources with chondritic Os isotopic compositions (e.g. Song La; Norseman-Wiluna; Pyke Hill; Alexo), though some (e.g. Gorgona) derive from heterogeneous sources. Of note, however, two ca. 2.7 Ga systems, Kostomuksha (Russia) and Belingwe (Zimbabwe), have initial ratios enriched by 2-3% relative to the contemporary convecting upper mantle. These results suggest that if the 187Os enrichment was due to the incorporation of minor amounts of recycled crust into the mantle source of the rocks, the crust formed very early in Earth history. Thus, the Os results could reflect derivation of melt from hybrid mantle whose composition was modified by the addition of mafic crustal material that would most likely have formed between 4.2 and 4.5 Ga. Alternately, the mantle sources of these komatiites may have derived a portion of their Os from the putative 187Os - and 186Os -enriched outer core. For this hypothesis to be applicable to Archean rocks, an inner core of sufficient mass would have to have crystallized sufficiently early in Earth history to generate an outer core with 187Os enriched by at least 3% relative to the chondritic average. Using the Pt-Re-Os partition coefficients espoused by our earlier work, and assuming linear growth of the inner core started at 4.5 Ga and continued to present, would yield an outer core at 2.7 Ga with a gamma Os value of only +1.2 and a 186Os/188Os enrichment relative to the contemporary upper mantle of only +13 ppm. Greater isotopic enrichments could have been achieved by 2.7 Ga if either the inner core comprised >2.8% of the mass of the core by 2.7 Ga, or if Re and Os solid metal-liquid metal D's for core crystallization were greater that those applied in the initial calculation.

Actualistic models of mantle metasomatism documented in a composite xenolith from Dish Hill, California

USGS Publications Warehouse

Nielson, J.E.; Budahn, J.R.; Unruh, D.M.; Wilshire, H.G.

1993-01-01

Major and trace-element whole rock and mineral variations in composite hornblendite-peridotite xenolith Ba-2-1, from Dish Hill, CA, are due to a single event of metasomatism in the mantle. The hornblendite is the crystallized selvage of a dike conduit charged with incompatible-element-enriched hydrous mafic magma. The magma infiltrated the refractory peridotite wallrock, reacted with its constituent minerals, and simultaneously deposited amphibole. The systematic data from this study show considerable variation in isotopic values and trace elements. These data provide insight into a mantle process that was defined previously from samples without context, lacking evidence about the number or source of metasomatic events. In the contact zone of Ba-2-1, peridotite is enriched in Fe, Ti, CO2) and H2O; clinopyroxene and amphibole also are enriched in Fe and Ti, but clinopyroxene appears slightly depleted in CaO. Compared to chondrites, peridotite, clinopyroxene, and probably amphibole are enriched in light rare earth (LREEcn) and other incompatible trace elements. Values of 87Sr 86Sr and 143Nd 144Nd in the contact zone are close to isotopic equilibrium with the dike. Whole rock and constituent clinopyroxene compositions change to those of refractory peridotite with distance from the contact. These compositional variations were modelled using Gresens' equation for whole-rock major and minor elements, and calculations for isotopic ratios and REEs, which emulate the effects of Chromatographic fractionation. The choice of endmembers was restricted to compositions actually present in mantle samples from Dish Hill. Model results indicate that: 1. (1) the variations can be explained as the result of a single metasomatic event, probably a single pulse of previously fractionated liquid; 2. (2) the ratio of total interacting liquid to peridotite was at least 1:3 by weight in the contact zone; and 3. (3) the composition of the metasomatic liquid changed progressively as it infiltrated beyond that zone. The small distance over which variations occur is due to the small amount of liquid that infiltrated. Only in the contact zone was peridotite wallrock saturated by a liquid composition similar to the dike. Comparison of the Ba-2-1 data with those of another xenolith from Dish Hill suggests that the compositional variations of mantle metasomatism result from both the compositional contrast between the metasomatizing liquid and wallrock and the relative abundances of each. Compositional and volumetric variations of mantle partial melts and their fractionates, and repeated events of melting and reaction in contiguous mantle, can create broad ranges of metasomatic "signatures" from the same process. ?? 1993.

Transition Metal Systematics of Opx-Enriched Harzburgites From the Cascades Arc With Implications for the Origin of Cratonic Peridotites

NASA Astrophysics Data System (ADS)

Turner, S. J.

2007-12-01

A number of peridotite xenoliths collected from the Simcoe volcanic field region of the Cascades arc exhibit notable enrichment of modal orthopyroxene. The process driving this enrichment is most likely metasomatism of the mantle wedge by Si-rich fluids derived ultimately from the underlying slab. By investigating the resultant elemental systematics associated with subduction zone metasomatism of this type, we hope to shed light on the origin of other opx-rich peridotites, such as those seen in many cratonic xenolith suites. The xenoliths found in the Simcoe volcanic field provide a rare opportunity to examine the composition of sub arc mantle, as it is unusual to find mantle xenoliths in volcanic arc lavas. The samples were analyzed using laser ablation ICPMS and their bulk compositions were reconstructed from point-counted mineral modes. Two-pyroxene mineral thermometry of the samples yield temperatures of approximately 1000 degrees C, corresponding to a depth of origin at uppermost mantle pressures if typical arc geotherms are assumed. Most of the peridotites are harzburgites or olivine-orthopyroxenites (Mg#s 0.88-0.9; opx mode 0.15-0.9), with small amounts of clinopyroxene (<0.02). Clinopyroxenes are significantly enriched in the light rare earths, consistent with a metasomatic origin for these opx-rich harzburgites. Of note is the counterintuitive systematics of Zn. Whole-rock Zn decreases with opx, but Zn in olivine also decreases with opx mode while Zn in opx increases with opx mode, hence the decrease in whole- rock Zn is not simply due to mechanical segregation of harzburgite into opx- and ol-rich zones. In summary, the REE signatures suggest the subducting slab as the most likely candidate for the source of the fluids that caused the opx enrichment. The opx-enrichment itself and the unusual trends in Zn suggest a reaction between a silicic fluid and normal harzburgite. Moreover, the concomitant decrease in olivine and whole-rock Zn with opx mode suggests significant leaching of Zn from the peridotite during this process. Because the bulk partitioning of Zn in anhydrous peridotite melting is unity, low Zn contents are anomalous. The best explanation for these low values is that Zn partition coefficients decrease in hydrous environments. Many opx-enriched Archean cratonic peridotite xenoliths have anomalously low Zn contents, supporting the suggestion that such peridotites formed in arc environments.

Gas geochemistry of the Valles caldera region, New Mexico and comparisons with gases at Yellowstone, Long Valley and other geothermal systems

USGS Publications Warehouse

Goff, F.; Janik, C.J.

2002-01-01

Noncondensible gases from hot springs, fumaroles, and deep wells within the Valles caldera geothermal system (210-300??C) consist of roughly 98.5 mo1% CO2, 0.5 mol% H2S, and 1 mol% other components. 3He/4He ratios indicate a deep magmatic source (R/Ra up to 6) whereas ??13C-CO2 values (-3 to -5???) do not discriminate between a mantle/magmatic source and a source from subjacent, hydrothermally altered Paleozoic carbonate rocks. Regional gases from sites within a 50-km radius beyond Valles caldera are relatively enriched in CO2 and He, but depleted in H2S compared to Valles gases. Regional gases have R/Ra values ???1.2 due to more interaction with the crust and/or less contribution from the mantle. Carbon sources for regional CO2 are varied. During 1982-1998, repeat analyses of gases from intracaldera sites at Sulphur Springs showed relatively constant CH4, H2, and H2S contents. The only exception was gas from Footbath Spring (1987-1993), which experienced increases in these three components during drilling and testing of scientific wells VC-2a and VC-2b. Present-day Valles gases contain substantially less N2 than fluid inclusion gases trapped in deep, early-stage, post-caldera vein minerals. This suggests that the long-lived Valles hydrothermal system (ca. 1 Myr) has depleted subsurface Paleozoic sedimentary rocks of nitrogen. When compared with gases from many other geothermal systems, Valles caldera gases are relatively enriched in He but depleted in CH4, N2 and Ar. In this respect, Valles gases resemble end-member hydrothermal and magmatic gases discharged at hot spots (Galapagos, Kilauea, and Yellowstone). Published by Elsevier Science B.V.

Influence of the interplanetary magnetic field on the occurrence and thickness of the plasma mantle

NASA Technical Reports Server (NTRS)

Sckopke, N.; Paschmann, G.; Rosenbauer, H.; Fairfield, D. H.

1976-01-01

The response of the plasma mantle to the orientation of the interplanetary magnetic field (IMF) has been studied by correlating Heos 2 plasma and Imp 6 magnetic field data. The mantle is nearly always present when the IMF has a southward component and often also when the field has a weak northward component. In addition, the mantle appears increasingly thicker with greater southward components. On the other hand, the mantle is thin or missing (from the region where it is normally found) when the average IMF has a strong northward component. This result supports the idea that polar cap convection plays a dominant role in the formation of the plasma mantle: mantle plasma originates in the magnetosheath, enters the magnetosphere through the day side polar cusps, and is transported across the cusp to the night side by means of a convection electric field whose magnitude is controlled by the orientation of the IMF.

Parental Sources of High-Alumina Alkaline Melts: Nd, Sr, Pb, and O Isotopic Evidence from the Devonian Kiya-Shaltyr Gabbro-Urtite Intrusion, South Siberia

NASA Astrophysics Data System (ADS)

Vrublevskii, V. V.; Gertner, I. F.; Chugaev, A. V.

2018-04-01

The isotope geochemistry (ɛNd( t) 4.8-5.4, 206Pb/204Pb in 18.05-18.36, 207Pb/204Pbin 15.53-15.57, 208Pb/204Pb in 37.59-37.83, 87Sr/86Sr( t) 0.7048-0.7057, δ18OSMOW 8-10.5‰) and trace element composition of the Kiya-Shaltyr gabbro-urtite pluton allow us to suggest a heterogeneous source and complex geodynamic settings of the Devonian alkali magmatism in the Kuznetsk Alatau. It is assumed that its evolution took place under conditions of partial mingling of matter of the depleted (PREMA) and enriched (EM) mantle with crustal contamination of the evolving melt. Such an interaction could have been a result of superposition of a mantle plume and an active margin (OIB and IAB components). In fold belts this led to the formation of hybrid high-alumina foidoite magmas.

Crustal Heat Production and the Thermal Evolution of Mars. Revision

NASA Technical Reports Server (NTRS)

McLennan, Scott M.

2001-01-01

The chemical compositions of soils and rocks from the Pathfinder site and Phobos-2 orbital gamma-ray spectroscopy indicate that the Martian crust has a bulk composition equivalent to large-ion lithophile (LIL) and heat-producing element (HPE) enriched basalt, with a potassium content of about 0.5%. A variety of radiogenic isotopic data also suggest that separation of LIL-enriched crustal and depleted mantle reservoirs took place very early in Martian history (greater than 4.0 Ga). Accordingly, if the enriched Martian crust is greater than 30km thick it is likely that a large fraction (up to at least 50%) of the heat-producing elements in Mars was transferred into the crust very early in the planet's history. This would greatly diminish the possibility of early widespread melting of the Martian mantle.

Evidence from the lamarck granodiorite for rapid late cretaceous crust formation in California

USGS Publications Warehouse

Coleman, D.S.; Frost, T.P.; Glazner, A.F.

1992-01-01

Strontium and neodymium isotopic data for rocks from the voluminous 90-million-year-old Lamarck intrusive suite in the Sierra Nevada batholith, California, show little variation across a compositional range from gabbro to granite. Data for three different gabbro intrusions within the suite are identical within analytical error and are consistent with derivation from an enriched mantle source. Recognition of local involvement of enriched mantle during generation of the Sierran batholith modifies estimates of crustal growth rates in the United States. These data indicate that parts of the Sierra Nevada batholith may consist almost entirely of juvenile crust added during Cretaceous magmatism.

Mantle melting and melt refertilization beneath the Southwest Indian Ridge: Mineral composition of abyssal peridotites

NASA Astrophysics Data System (ADS)

Chen, Ling; Zhu, Jihao; Chu, Fengyou; Dong, Yan-hui; Liu, Jiqiang; Li, Zhenggang; Zhu, Zhimin; Tang, Limei

2017-04-01

As one of the slowest spreading ridges of the global ocean ridge system, the Southwest Indian Ridge (SWIR) is characterized by discontinued magmatism. The 53°E segment between the Gallieni fracture zone (FZ) (52°20'E) and the Gazelle FZ (53°30'E) is a typical amagmatic segment (crustal thickness <2km) (Zhou and Dick, 2013) that opens a window to the mantle thus provides a chance to detect the mantle composition directly. We examine the mineral compositions of 17 peridotite samples from the 53°E amagmatic segment. The results show that the peridotites can be divided into two groups. The Group 1 peridotites are characterized by clinopyroxenes having LREE depleted patterns that is typical for the abyssal peridotite, thus are thought to be the residue of the mantle melting. The Group 2 peridotites show the lowest HREE content within the SWIR peridotites but are anomaly enriched in LREE, with flat or U-type REE patterns, thus cannot be the pure residue of mantle melting. Mineral compositions of the Group 2 peridotites are more depleted than that of peridotites sampled near the Bouvet hot spot (Johnson et al., 1990), implying that the depleted mantle beneath the 53°E segment may be the residue of ancient melting event. This hypothesis is supported by the the low Ol/Opx ratios, coarse grain sizes (>1cm) Opx, and Mg-rich mineral compositions akin to harzburgite xenoliths that sample old continental lithospheric mantle (Kelemen et al., 1998). Melt refertilization model shows that Group 2 peridotites were affected by an enriched low-degree partial melt from the garnet stability field. These results indicate that depleted mantle which experiences ancient melting event are more sensitive to melt refertilization, thus may reduce the melt flux, leading to extremely thin crust at 53°E segment. This research was granted by the National Basic Research Programme of China (973 programme) (grant No. 2013CB429705) and the Fundamental Research Funds of Second Institute of Oceanography, State Oceanic Administration (JG1603, SZ1507). References: Johnson K T M, Dick H J B, Shimizu N. Melting in the oceanic upper mantle: An ion microprobe study of diopsides in abyssal peridotites[J]. Journal of Geophysical Research, 1990, 95(B3):2661-2678. Kelemen P B, Hart S R, Bernstein S. Silica enrichment in the continental upper mantle via melt/rock reaction[J]. Earth & Planetary Science Letters, 1998, 164(1-2):387-406. Zhou H, Dick H J. Thin crust as evidence for depleted mantle supporting the Marion Rise.[J]. Nature, 2013, 494(7436):195-200.

Mantle sources and magma evolution of the Rooiberg lavas, Bushveld Large Igneous Province, South Africa

NASA Astrophysics Data System (ADS)

Günther, T.; Haase, K. M.; Klemd, R.; Teschner, C.

2018-06-01

We report a new whole-rock dataset of major and trace element abundances and 87Sr/86Sr-143Nd/144Nd isotope ratios for basaltic to rhyolitic lavas from the Rooiberg continental large igneous province (LIP). The formation of the Paleoproterozoic Rooiberg Group is contemporaneous with and spatially related to the layered intrusion of the Bushveld Complex, which stratigraphically separates the volcanic succession. Our new data confirm the presence of low- and high-Ti mafic and intermediate lavas (basaltic—andesitic compositions) with > 4 wt% MgO, as well as evolved rocks (andesitic—rhyolitic compositions), characterized by MgO contents of < 4 wt%. The high- and low-Ti basaltic lavas have different incompatible trace element ratios (e.g. (La/Sm)N, Nb/Y and Ti/Y), indicating a different petrogenesis. MELTS modelling shows that the evolved lavas are formed by fractional crystallization from the mafic low-Ti lavas at low-to-moderate pressures ( 4 kbar). Primitive mantle-normalized trace element patterns of the Rooiberg rocks show an enrichment of large ion lithophile elements (LILE), rare-earth elements (REE) and pronounced negative anomalies of Nb, Ta, P, Ti and a positive Pb anomaly. Unaltered Rooiberg lavas have negative ɛNdi (- 5.2 to - 9.4) and radiogenic ɛSri (6.6 to 105) ratios (at 2061 Ma). These data overlap with isotope and trace element compositions of purported parental melts to the Bushveld Complex, especially for the lower zone. We suggest that the Rooiberg suite originated from a source similar to the composition of the B1-magma suggested as parental to the Bushveld Lower Zone, or that the lavas represent eruptive successions of fractional crystallization products related to the ultramafic cumulates that were forming at depth. The Rooiberg magmas may have formed by 10-20% crustal assimilation by the fractionation of a very primitive mantle-derived melt within the upper crust of the Kaapvaal Craton. Alternatively, the magmas represent mixtures of melts from a primitive, sub-lithospheric mantle plume and an enriched sub-continental lithospheric mantle (SCLM) component with harzburgitic composition. Regardless of which of the two scenarios is invoked, the lavas of the Rooiberg Group show geochemical similarities to the Jurassic Karoo flood basalts, implying that the Archean lithosphere strongly affected both of these large-scale melting events.

Petroleum formation during serpentinization: the evidence of trace elements

NASA Astrophysics Data System (ADS)

Szatmari, P.; Fonseca, T. C.; Miekeley, N. F.

2002-05-01

An organic source of petroleum formation is well attested by many biomarkers. This need not, however, exclude contribution from inorganic sources. During serpentinization, in the absence of free oxygen, oxidation of bivalent Fe to magnetite breaks up the water molecule, generating hydrogen and creating one of the most reducing environments near the Earth's surface (Janecky & Seyfried, 1986). Szatmari (1989) proposed that some petroleum forms at plate boundaries by Fischer-Tropsch-type synthesis over serpentinizing peridotites and suggested that Ni, an element rare in the continental crust but important in both petroleum and the mantle, may be indicative of such a source. Recently, Holm and Charlou (2001) observed hydrocarbon formation by Fischer-Tropsch-type synthesis over serpentinizing peridotites of the Mid-Atlantic Ridge. To test whether the relative amounts of other trace elements in petroleum are in agreement with a serpentinizing source, we analyzed by internally coupled plasma-mass spectroscopy (ICP-MS) 22 trace elements in 68 oils sampled in seven sedimentary basins throughout Brazil. We found that trace elements in the oils correlate well with mantle peridotites and reflects the process of hydrothermal serpentinization during continental breakup. Four groups may be distinguished. In serpentinites, trace elements of the first group, Ti, Cr, Mn, and Fe, are largely retained in low-solubility magnetite and other spinels formed during serpentinization or inherited from the original peridotites. In the oils, when normalized to mantle peridotites, these elements are at relatively low levels, about 10,000 times less than their abundances in mantle peridotites, reflecting their low availability from stable minerals. In contrast, trace elements of the second group, which includes V, Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Ba, La, Ce, and Nd, pass during serpentinization mostly into serpentine minerals or solution. In the oils, when normalized to mantle peridotites, these elements are at higher levels than those of the first group, about 300 times less than their abundances in mantle peridotites, reflecting their higher availability during serpentinization. Within both groups, trace metal ratios and A/(A+B) type proportionalities in the oils are close to mantle peridotites. V behaves somewhat differently: in lacustrine sequences V contents in the oils are low and the ratios of V to other elements of the second group are mantle-like, whereas in marine sequences V and its ratios to other trace elements rise by orders of magnitude. Trace elements commonly enriched in formation fluids and hydrothermal brines (Rb, Sr, Ba, Cu, Zn), when normalized to mantle peridotites, are enriched in the oils by about 0.5 order of magnitude relative to other elements of the second group. The third group of elements includes S, Mo, and As. These elements occur in the oils at abundances similar to sea water and are, when normalized to mantle peridotites and Ni, enriched in the oils by several orders of magnitude, indicating sea water reacting with peridotites during sepentinization as their possible source. Finally trace elements of the fourth group, such as Pb and Ag, are enriched in the oils by several orders of magnitude relative to both mantle peridotites and sea water and were presumably mobilized from shales by hydrothermal fluids. References:Holm, N.G. and Charlou, J.L., 2001, EPSL 191, 1-8. Janecky, D.R. and Seyfried, W.E., 1986, Geochim. Cosmochim. Acta 50, 1357-1378. Szatmari, P., 1989, AAPG Bull. 73, 989-998.

Origin of depleted components in basalt related to the Hawaiian hot spot: Evidence from isotopic and incompatible element ratios

NASA Astrophysics Data System (ADS)

Frey, F. A.; Huang, S.; Blichert-Toft, J.; Regelous, M.; Boyet, M.

2005-02-01

The radiogenic isotopic ratios of Sr, Nd, Hf, and Pb in basaltic lavas associated with major hot spots, such as Hawaii, document the geochemical heterogeneity of their mantle source. What processes created such heterogeneity? For Hawaiian lavas there has been extensive discussion of geochemically enriched source components, but relatively little attention has been given to the origin of depleted source components, that is, components with the lowest 87Sr/86Sr and highest 143Nd/144Nd and 176Hf/177Hf. The surprisingly important role of a depleted component in the source of the incompatible element-enriched, rejuvenated-stage Hawaiian lavas is well known. A depleted component also contributed significantly to the ˜76-81 Ma lavas erupted at Detroit Seamount in the Emperor Seamount Chain. In both cases, major involvement of MORB-related depleted asthenosphere or lithosphere has been proposed. Detroit Seamount and rejuvenated-stage lavas, however, have important isotopic differences from most Pacific MORB. Specifically, they define trends to relatively unradiogenic Pb isotope ratios, and most Emperor Seamount lavas define a steep trend of 176Hf/177Hf versus 143Nd/144Nd. In addition, lavas from Detroit Seamount and recent rejuvenated-stage lavas have relatively high Ba/Th, a characteristic of lavas associated with the Hawaiian hot spot. It is possible that a depleted component, intrinsic to the hot spot, has contributed to these young and old lavas related to the Hawaiian hot spot. The persistence of such a component over 80 Myr is consistent with a long-lived source, i.e., a plume.

Isotopic decoupling during porous melt flow: A case-study in the Lherz peridotite

NASA Astrophysics Data System (ADS)

Le Roux, V.; Bodinier, J.-L.; Alard, O.; O'Reilly, S. Y.; Griffin, W. L.

2009-03-01

Most peridotite massifs and mantle xenoliths show a wide range of isotopic variations, often involving significant decoupling between Hf, Nd and Sr isotopes. These variations are generally ascribed either to mingling of individual components of contrasted isotopic compositions or to time integration of parent-element enrichment by percolating melts/fluids, superimposed onto previous depletion event(s). However, strong isotopic decoupling may also arise during porous flow as a result of daughter-elements fractionation during solid-liquid interaction. Although porous flow is recognized as an important process in mantle rocks, its effects on mantle isotopic variability have been barely investigated so far. The peridotites of the Lherz massif (French Pyrenees) display a frozen melt percolation front separating highly refractory harzburgites from refertilized lherzolites. Isotopic signatures observed at the melt percolation front show a strong decoupling of Hf from Nd and Sr isotopes that cannot be accounted for by simple mixing involving the harzburgite protolith and the percolating melt. Using one dimensional percolation-diffusion and percolation-reaction modeling, we show that these signatures represent transient isotopic compositions generated by porous flow. These signatures are governed by a few critical parameters such as daughter element concentrations in melt and peridotite, element diffusivity, and efficiency of isotopic homogenization rather than by the chromatographic effect of melt transport and the refertilization reaction. Subtle variations in these parameters may generate significant inter-isotopic decoupling and wide isotopic variations in mantle rocks.

Carbon and its isotopes in mid-oceanic basaltic glasses

USGS Publications Warehouse

Des Marais, D.J.; Moore, J.G.

1984-01-01

Three carbon components are evident in eleven analyzed mid-oceanic basalts: carbon on sample surfaces (resembling adsorbed gases, organic matter, or other non-magmatic carbon species acquired by the glasses subsequent to their eruption), mantle carbon dioxide in vesicles, and mantle carbon dissolved in the glasses. The combustion technique employed recovered only reduced sulfur, all of which appears to be indigenous to the glasses. The dissolved carbon concentration (measured in vesicle-free glass) increases with the eruption depth of the spreading ridge, and is consistent with earlier data which show that magma carbon solubility increases with pressure. The total glass carbon content (dissolved plus vesicular carbon) may be controlled by the depth of the shallowest ridge magma chamber. Carbon isotopic fractionation accompanies magma degassing; vesicle CO2 is about 3.8??? enriched in 13C, relative to dissolved carbon. Despite this fractionation, ??13CPDB values for all spreading ridge glasses lie within the range -5.6 and -7.5, and the ??13CPDB of mantle carbon likely lies between -5 and -7. The carbon abundances and ??13CPDB values of Kilauea East Rift glasses apparently are influenced by the differentiation and movement of magma within that Hawaiian volcano. Using 3He and carbon data for submarine hydrothermal fluids, the present-day mid-oceanic ridge mantle carbon flux is estimated very roughly to be about 1.0 ?? 1013 g C/yr. Such a flux requires 8 Gyr to accumulate the earth's present crustal carbon inventory. ?? 1984.

Evolution of the lithospheric mantle beneath Mt. Baekdu (Changbaishan): Constraints from geochemical and Sr-Nd-Hf isotopic studies on peridotite xenoliths in trachybasalt

NASA Astrophysics Data System (ADS)

Park, Keunsu; Choi, Sung Hi; Cho, Moonsup; Lee, Der-Chuen

2017-08-01

Major and trace element compositions of minerals as well as Sr-Nd-Hf isotopic compositions of clinopyroxenes from spinel peridotite xenoliths entrained in Late Cenozoic trachybasalt from Mt. Baekdu (Changbaishan) were used to elucidate lithospheric mantle formation and evolution in the eastern North China Craton (NCC). The analyzed peridotites were mainly spinel lherzolites with rare harzburgites. They consisted of olivine (Fo89.3-91.0), enstatite (Wo1-2En88-90Fs8-11), diopside (Wo45-50En45-51Fs4-6), and spinel (Cr# = 8.8-54.7). The peridotite residues underwent up to 25% partial melting in fertile mid-ocean-ridge basalt (MORB) mantle. Plots of the Cr# in spinel against the Mg# in coexisting olivine or spinel suggested an affinity with abyssal peridotites. Comparisons of Cr# and TiO2 in spinel were also compatible with an abyssal peridotite-like composition; however, harzburgites were slightly enriched in TiO2 because of the reaction with MORB-like melt. Temperatures estimated using two-pyroxene thermometry ranged from 750 to 1010 °C, reflecting their lithospheric mantle origin. The rare earth element (REE) patterns in clinopyroxenes of the peridotites varied from light REE (LREE) depleted to spoon shaped to LREE enriched, reflecting secondary overprinting effects of metasomatic melts or fluids on the residues from primordial melting. The calculated trace element pattern of metasomatic melt equilibrated with clinopyroxene in Mt. Baekdu peridotite showed strong enrichment in large-ion lithophile elements, Th and U together with slight fractionation in heavy REEs (HREEs) and considerable depletion in Nb and Ti. The Sr-Nd-Hf isotopic compositions of clinopyroxenes separated from the peridotites varied from more depleted than present-day MORB to bulk Earth values. However, some clinopyroxene showed a decoupling between Nd and Sr isotopes, deviating from the mantle array with a high 87Sr/86Sr ratio. This sample also showed a significant Nd-Hf isotope decoupling lying well above the mantle array. The Lu-Hf and Sm-Nd model ages of residual clinopyroxenes yielded Early Proterozoic to Phanerozoic ages. No signature of Archean cratonic mantle was present. Therefore, Mt. Baekdu peridotite is residual lithospheric mantle that has undergone variable degrees of diachronous melt extraction and infiltration metasomatism involving subduction-related, fluid-bearing silicate melts. The predominance of Phanerozoic Hf model ages indicates that the lherzolites represent lithospheric mantle fragments newly accreted underneath the eastern NCC.

Mechanisms of formation of mantle section pyroxenites of Voykar Ophiolite, Polar Urals, Russia

NASA Astrophysics Data System (ADS)

Belousov, Ivan; Batanova, Valentina; Sobolev, Alexander; Savelieva, Galina

2010-05-01

Ural Mountains mark a major mid Paleozoic collision event, which resulted in the closure of an ocean basin separating the Siberian and European plates. Voykar Ophiolite is located in the Northern part of Uralian Ophiolite Belt. Ophiolitic sequence rocks of Polar Urals are usually considered as giant fragments of mantle and MORB-type crust formed in back-arc settings (e.g. Savelieva et al., 1987). Mantle section of Voykar Ophiolite comprises most of the ophiolitic sequence. It is up to 8 km thick and consists mostly of spinel harzburgites with multiple dunitic bodies and pyroxenitic veins representing pathways for different melts/fluids. While it is generally accepted that dunites in mantle sections are formed by melt-rock reaction and mark melt pathways (e.g. Kelemen et al., 1995), formation of pyroxenites is a subject of debate. Often pyroxenites from mantle sections of ophiolites (Varfalvy et al., 1997), as well as pyroxenites from mantle wedge xenoliths (Arai et al., 2006, Bali et al., 2007, Gregoire et al., 2008) are interpreted as interaction products between high-SiO2 melts and mantle peridotites. Such melts are believed to be widespread in SSZ mantle: boninites, high-MgO andesites and adakites. However, some researchers (e.g. Berly et al., 2006, Halama et al., 2009) propose pyroxenite formation in metasomatic reaction with fluid from subducting plate. Moreover, some pyroxenites could be formed by the melt crystallization in hydrous conditions (Muntener et al., 2001). We present comprehensive study of mineral major and trace element compositions from the mantle section rocks of Voykar Ophiolite in order to determine mechanism of formation of pyroxenites in ophiolitic mantle sections. Compositions of clinopyroxene and olivine from pyroxenites were compared to their compositions in harzburgites and dunites. Furthermore, compositions of clinopyroxene and magmatic amphibole from mantle section pyroxenites were used to calculate equilibrium melts. Geochemical data (enrichment of clinopyroxenes and amphiboles in LREE and LILE (Rb, Ba, Sr) relative to HFSE (Nb, Zr)) together with structural data suggests that pyroxenites display clear suprasubduction signatures and refer to the last stage of Voykar Ophiolite mantle section formation. All minerals from pyroxenites tend to have lower Mg-numbers and, therefore, high-Si meltsfluids have played major role in their formation. Depletion of clinopyroxenes in HREE and enrichment in Sr and LREE across the harzburgite-pyroxenite contacts suggests that this high-Si melts most probably refer to depleted SSZ melts, such as boninites. One group of magmatic amphibole in pyroxenites refers to such melts. However, another group of magmatic amphiboles probably refers to high-Si fluid depleted in REE and enriched in LILE (Rb, Ba, Sr) and Pb. Therefore, the variety of pyroxenite segregations, veins, and dikes reflects progressive stages of melt/fluid migration through harzburgite and dunite at various P-T conditions. For some pyroxenites (such as zoned websterite dikes) formation by fractional crystallization of hydrous magmas couldn't be excluded.

Elemental and Sr-Nd isotopic geochemistry of the Uradzhongqi magmatic complex in western Inner Mongolia, China: A record of early Permian post-collisional magmatism

NASA Astrophysics Data System (ADS)

Qiao, Xueyuan; Li, Wenbo; Zhong, Richen; Hu, Chuansheng; Zhu, Feng; Li, Zhihua

2017-08-01

The magmatic complex in Uradzhongqi, Inner Mongolia, is located in the western segment of the northern margin of the North China Craton (NCC). The dominant components in the complex include syenogranite, monzogranite, granodiorite, diorite and gabbro. Mafic microgranular enclaves (MMEs) are common in syenogranite and granodiorite. Zircon U-Pb dating shows that the ages of these rocks range from 283 to 270 Ma, suggesting an early Permian emplacement. The syenogranite and monzogranite are peraluminous I-type granites, exhibiting conspicuous negative Eu anomaly, enrichment in large-ion lithophile elements (LILE) and light rare earth elements (LREE), depletion in high field strength elements (HFSE). The granodiorites, diorites and MMEs are metaluminous in composition, show high Al2O3, MgO and Fe2O3T contents and weak negative Eu anomaly, as well as LREE and LILE enrichment and HFSE depletion. The gabbros show weak positive Eu anomaly and slight REE differentiation. The Sr-Nd isotope compositions show that the source of mafic magma was depleted mantle (DM) with possible involvement of enriched mantle II (EM II), whereas the felsic magma was derived from the Archean lower crust. Petrographic observation and analytical results of mineralogy, geochronology, geochemistry and Sr-Nd isotopes indicate that the main petrogenesis of these magmatic rocks is the mixing of underplating mafic magma and felsic magma. Tectonically, the complex pluton was formed within a post-collisional regime, and the underplating in this area provides another piece of evidence for the vertical growth of the western segment of the northern margin of the NCC.

B, Sr and Pb isotope geochemistry of high-pressure Alpine metaperidotites monitors fluid-mediated element recycling during serpentinite dehydration in subduction mélange (Cima di Gagnone, Swiss Central Alps)

NASA Astrophysics Data System (ADS)

Cannaò, E.; Agostini, S.; Scambelluri, M.; Tonarini, S.; Godard, M.

2015-08-01

Tectonic mixing of slab- and mantle-derived materials at the interface between converging plates highly enhances fluid-mediated mass transfer from the slab to the overlying mantle. Subduction mélanges can provide information about the interaction among different slices accreted at plate interface domains, with implications on the tectonic and geochemical evolution of the plate-interface itself. At Cima di Gagnone, pelitic schists and gneiss enclose chlorite harzburgite and garnet peridotite lenses, like in subduction mélanges located in-between downgoing slabs and overlying mantle. These peridotites host MORB-type eclogite and metarodingite, and derive from dehydration of serpentinized mantle protoliths. Their enrichment in fluid-mobile B, As, Sb, U, Th is the result of an early-stage oceanic serpentinization, followed by interaction with host metasediments during subduction burial. Here we define the element exchange process in the Gagnone mélange by means of the B, Sr and Pb isotope analysis of its main lithologies (ultramafic, mafic rocks and paragneiss). The 87Sr/86Sr and 206Pb/204Pb ratios of ultramafic rocks (0.7090-0.7124 and 18.292-18.837, respectively) show enrichments in radiogenic Sr and Pb after exchange with the host paraschist (up to 0.7287 87Sr/86Sr; 18.751 206Pb/204Pb). The δ11B values of peridotites (down to -10‰) point to a combined effect of (1) 11B release to deserpentinization fluids (serpentinized protoliths likely had positive δ11B and lower radiogenic Sr, Pb), and of (2) exchange with fluids from the surrounding metasediments. The whole Gagnone rock-suite is finally overprinted by retrograde fluids that essentially bring to an increase in radiogenic Pb (about 19.0 206Pb/204Pb) and to values of 0.710 87Sr/86Sr and of -10‰ δ11B. The recognition of different stages of interaction between mantle rocks and sedimentary/crustal reservoirs allows us to define the geochemical effects related to the early coupling of such rocks along the plate-interface. Our study shows that ultramafic rocks involved in subduction-zone metamorphism and serpentinization uptake radiogenic Pb and Sr released by associated sedimentary reservoirs. The exchange process envisioned here is not only representative of subduction mélanges: it can also be a proxy of mass transfer between slab and serpentinized supra-subduction mantle, as occurs in forearcs. Dehydration of the Gagnone-type serpentinized mantle releases crust-derived components to arcs, without direct involvement of metasediment dehydration and/or melting in subarc environments. The retention of appreciable amounts of fluid-mobile elements, radiogenic Pb and Sr in dehydrated Gagnone peridotites has implications on element recycling in the deep Earth's mantle.

A Xenolith Perspective on the Composition and Age of the Northern Tanzanian Lithosphere (Invited)

NASA Astrophysics Data System (ADS)

Rudnick, R. L.; Aulbach, S.; Bellucci, J. J.; Blondes, M. S.; Chesley, J.; Lee, C.; Mansur, A. T.; Manya, S.; McDonough, W. F.

2009-12-01

Study of deep crustal and upper mantle xenoliths from rift volcanoes throughout northern Tanzania provides insights into the architecture of the Tanzanian lithosphere, as well as the interaction of this lithosphere with rift magmas. Like the upper crust, the lower crust and mantle lithosphere of the Tanzanian Craton (TC) and Mozambique Belt (MB) are Archean, but the lower crust of the MB has been thermally reactivated during the pan-African Orogeny, whereas that of the craton has not. In addition, both mantle sections have experienced interaction and heating associated with rift magmas. Cratonic lithospheric mantle is compositionally stratified, with highly refractory but strongly LREE-enriched peridotite comprising the bulk of the section (40-130 km depth), underlain by more fertile and deformed peridotites (130-150 km depth), which are also LREE-enriched. Lithospheric mantle of the MB is highly variable in thickness, ranging from a maximum of ˜150 km at Lashaine to <50 km within the Rift axis near the Kenyan border. Like the cratonic lithosphere, this mantle is also refractory and yields Archean Os model ages throughout. Mantle lithospheres of both the TC and MB have interacted with rift magmas, including carbonatites (at Olmani) and alkali basalts (s.l.), which, in some cases, precipitated veins containing phlogopite or amphibole. Late Pleistocene zircons in one of these veins testify to the youth of this interaction. Rift basalt precipitates that formed in the mantle (pyroxenites and glimmerites) and have, thus, never interacted with continental crust, have radiogenic Os isotopic compositions (γOs = +9), providing strong evidence for a plume source of the rift magmas. Sr and Nd isotopes in cpx from peridotites are highly variable: in some they are completely overprinted by rift magmas, whereas others contain Archean components. Granulite-facies xenoliths throughout northern Tanzania are generally mafic (including anorthositic compositions), with a few intermediate compositions; no granulite-facies metapelites have been found. Marbles, schists, quartzites and amphibolites from the MB likely derive from middle-crustal depths. All zircon U-Pb ages are Archean (≥ 2.6 Ga) and many of the samples fall along a 2.6 Ga Sm-Nd reference line. U-Pb thermochronology largely records slow cooling in the MB following the Pan-African Orogeny and is consistent with a present-day conductive geotherm of 47 mW/m2 in a crust with very low heat production (see Blondes et al., this meeting). Despite the fact that ɛNd varies from -4 to -32 in the lower crustal xenoliths, 87Sr/86Sr is much less variable and the data fall along a near-vertical trend in a Sr vs. Nd isotope plot, reflecting ancient Rb depletion relative to Sr. Similarly, the unradiogenic Pb in granulite feldspars from both TC and MB is consistent with ancient U depletion. Collectively, such distinctive radiogenic isotope characteristics can serve as a diagnostic signature of crustal assimilation in rift magmas from northern Tanzania.

Pre-subduction metasomatic enrichment of the oceanic lithosphere induced by plate flexure

NASA Astrophysics Data System (ADS)

Pilet, S.; Abe, N.; Rochat, L.; Kaczmarek, M.-A.; Hirano, N.; Machida, S.; Buchs, D. M.; Baumgartner, P. O.; Müntener, O.

2016-12-01

Oceanic lithospheric mantle is generally interpreted as depleted mantle residue after mid-ocean ridge basalt extraction. Several models have suggested that metasomatic processes can refertilize portions of the lithospheric mantle before subduction. Here, we report mantle xenocrysts and xenoliths in petit-spot lavas that provide direct evidence that the lower oceanic lithosphere is affected by metasomatic processes. We find a chemical similarity between clinopyroxene observed in petit-spot mantle xenoliths and clinopyroxene from melt-metasomatized garnet or spinel peridotites, which are sampled by kimberlites and intracontinental basalts respectively. We suggest that extensional stresses in oceanic lithosphere, such as plate bending in front of subduction zones, allow low-degree melts from the seismic low-velocity zone to percolate, interact and weaken the oceanic lithospheric mantle. Thus, metasomatism is not limited to mantle upwelling zones such as mid-ocean ridges or mantle plumes, but could be initiated by tectonic processes. Since plate flexure is a global mechanism in subduction zones, a significant portion of oceanic lithospheric mantle is likely to be metasomatized. Recycling of metasomatic domains into the convecting mantle is fundamental to understanding the generation of small-scale mantle isotopic and volatile heterogeneities sampled by oceanic island and mid-ocean ridge basalts.

High H2O/Ce of K-rich MORB from Lena Trough and Gakkel Ridge, Arctic Ocean

NASA Astrophysics Data System (ADS)

Snow, J. E.; Feig, S. T.

2014-12-01

Lena Trough in the Arctic ocean is the oblique spreading continuation of Gakkel Ridge through the Fram Strait (eg Snow et al. 2011). Extreme trace element and isotopic compositions seen in Lena Trough basalt appear to be the enriched end member dominating the geochemistry of the Western Volcanic Zone of the Western Gakkel Ridge as traced by Pb isotopes, K2O/TiO2, Ba/Nb and other isotopic, major and trace element indicators of mixing (Nauret et al., 2011). This is in contrast to neighboring Gakkel Ridge which has been spreading for 50-60 million years. Basalts from Lena Trough also show a pure MORB noble gas signature (Nauret et al., 2010) and peridotites show no evidence of ancient components in their Os isotopes (Lassiter, et al., in press). The major and trace element compositions of the basalts, however are very distinct from MORB, being far more potassic than all but a single locality on the SW Indian Ridge. We determined H2O and trace element composiitions of a suite of 17 basalt glasses from the Central Lena Trough (CLT) and the Gakkel Western Volcanic Zone, including many of those previously analyzed by Nauret et al. (2012). The Western Gakkel glasses have high H2O/Ce for MORB (>300) suggesting a water rich source consistent with the idea that the northernmost Atlantic mantle is enriched in water (Michael et al., 1995). They are within the range of Eastern Gakkel host glasses determined by Wanless et al, 2013. The Lena Trough (CLT) glasses are very rich in water for MORB (>1% H2O) and are among the highest H2O/Ce (>400) ever measured in MORB aside from melt inclusions in olivine. Mantle melting dynamics and melt evolution cannot account for the H2O/Ce variations in MORB, as these elements have similar behavior during melting and crustal evolution. Interestingly, the H2O/K2O ratios in the basalts are only around 1. This is because the K2O levels in the CLT glasses are very high as well relative to REE. The absolutely linear relationship between H2O and K2O/TiO2 in Lena and Gakkel basalts shows that water systematics in these rocks are completely governed by source composition, with little or no modification by mantle melting dynamics or crystal fractionation. The geochemical influence of the WVZ enriched mantle source declines with distance from Lena Trough along Gakkel Ridge.

Constraints on Thermochemical Convection of the Mantle from Plume-related Observations

NASA Astrophysics Data System (ADS)

Zhong, S.

2005-05-01

Although geochemical observations have long suggested a layered mantle with more enriched mantle material in the bottom layer to provide a significant amount of heat to the top layer, the nature of such a layering remains unclear. An important observation that has been used to argue against the conventional layered mantle model (i.e., the layering at the 670 km depth) was the plume heat flux [Davies, 1999]. Plume heat flux is estimated as ~ 3.5 TW, or 10% of the surface heat flux [Davies, 1988; Sleep, 1990]. In this study, we demonstrate with 3-D spherical models of mantle convection with depth- and temperature-dependent viscosity that observed plume heat flux, plume excess temperature (<350°C), and upper mantle temperature (~ 1300°C) can pose important constraints on the layered mantle convection. We show that for a purely thermal convection model (i.e., a whole mantle convection), the observations of plume heat flux, plume excess temperature, and upper mantle temperature can be simultaneously explained only when internal heating rate is about 65%. For smaller internal heating rate, plume heat flux and plume excess temperature would be too large, and upper mantle temperature would be too small, compared with the observed. This suggests that for a whole mantle convection the CMB heat flux needs to be > 10 TW. For a core with no significant heat producing elements, such large CMB heat flux may lead to too rapid cooling of the core or a too young inner core. A layered mantle convection may help reduce the CMB heat flux. For layered convection models, we found that the top layer needs to be ~70% internally heated to explain the upper mantle temperature and plume-related observations, and this required internal heating ratio is insensitive to the layer thickness for the bottom layer (we used ~600 km and 1100 km thicknesses). This result suggests that heat generation rate for the bottom layer cannot be significantly larger (< a factor of 2) than that for the top layer. thus challenging the conventional geochemical inference for an significantly enriched bottom layer. However, this is more consistent with recent estimate of the MORB source composition that increases heat producing element concentration by a factor of three compared with the previously proposed.

Linking the tectonic evolution with fluid history in magma-poor rifted margins: tracking mantle- and continental crust-related fluids

NASA Astrophysics Data System (ADS)

Pinto, V. H. G.; Manatschal, G.; Karpoff, A. M.

2014-12-01

The thinning of the crust and the exhumation of subcontinental mantle is accompanied by a series of extensional detachment faults. Exhumation of mantle and crustal rocks is intimately related to percolation of fluids along detachment faults leading to changes in mineralogy and chemistry of the mantle, crustal and sedimentary rocks. Field observation, analytical methods, refraction/reflection and well-core data, allowed us to investigate the role of fluids in the Iberian margin and former Alpine Tethys distal margins and the Pyrenees rifted system. In the continental crust, fluid-rock interaction leads to saussuritization that produces Si and Ca enriched fluids found in forms of veins along the fault zone. In the zone of exhumed mantle, large amounts of water are absorbed in the first 5-6 km of serpentinized mantle, which has the counter-effect of depleting the mantle of elements (e.g., Si, Ca, Mg, Fe, Mn, Ni and Cr) forming mantle-related fluids. Using Cr-Ni-V and Fe-Mn as tracers, we show that in the distal margin, mantle-related fluids used detachment faults as pathways and interacted with the overlying crust, the sedimentary basin and the seawater, while further inward parts of the margin, continental crust-related fluids enriched in Si and Ca impregnated the fault zone and may have affected the sedimentary basin. The overall observations and results enable us to show when, where and how these interactions occurred during the formation of the rifted margin. In a first stage, continental crust-related fluids dominated the rifted systems. During the second stage, mantle-related fluids affected the overlying syn-tectonic sediments through direct migration along detachment faults at the future distal margin. In a third stage, these fluids reached the seafloor, "polluted" the seawater and were absorbed by post-tectonic sediments. We conclude that a significant amount of serpentinization occurred underneath the thinned continental crust, that the mantle-related fluids might have modified the chemical composition of the sediments and seawater. We propose that the chemical signature of serpentinization that occurs during the mantle exhumation is recorded in the sediments and may serve as a proxy to date serpentinization and mantle exhumation in present day magma-poor rifted margins.

Tradeoffs in Chemical and Thermal Variations in the Post-perovskite Phase Transition: Mixed Phase Regions in the Deep Lower Mantle?

NASA Astrophysics Data System (ADS)

Giles, G. F.; Spera, F. J.; Yuen, D. A.

2005-12-01

The recent discovery of a phase-transition in Mg-rich perovskite (Pv) to a post-perovskite (pPv) phase at lower mantle depths and its relationship to D", lower mantle heterogeneity and iron content prompted an investigation of the relative importance of lower mantle (LM) compositional and temperature fluctuations in creating topographic undulations on mixed phase regions. Above the transition, Mg-rich Pv makes up ~70 percent by mass of the LM. Using results from experimental phase equilibria, first-principles computations and thermodynamic relations for Fe2+-Mg mixing in silicates, a preliminary thermodynamic model for the perovskite to post-perovskite phase transition in the divariant system MgSiO3-FeSiO3 is developed. Complexities associated with components Fe2O3 and Al2O3 and other phases (Ca-Pv, magnesiowustite) are neglected. The model predicts phase transition pressures are sensitive to the FeSiO3 content of perovskite (~-1.5 GPa per one mole percent FeSiO3). This leads to considerable topography along the top boundary of the mixed phase region. The Clapeyron slope for the Pv to pPv transition at XFeSiO3=0.1 is +11 MPa/K about 20% higher than for pure Mg-Pv. Increasing bulk concentration of iron elevates the mixed (two-phase) layer above the core-mantle boundary (CMB); increasing temperature acts to push the mixed layer deeper into the LM into the D" thermal boundary layer resting upon the (CMB). For various LM geotherms and CMB temperatures, a single mixed layer of thickness ~300 km lies within the bottom 40% of the lower mantle. For low iron contents (XFeSiO3 ~5 mole percent or less), two perched layers are found. This is the divariant analog to the univariant double-crosser. The hotter the mantle, the deeper the mixed phase layer; the more iron-rich the LM, the higher the mixed phase layer. In a hotter Hadean Earth with interior temperatures everywhere 200-500 K warmer pPv is not stable unless the LM bulk composition is Fe-enriched compared to the present upper mantle.

Quaternary Basanitic Rocks within the Eastern Anatolian Volcanism (Turkey): Petrological and Geochemical Constrains

NASA Astrophysics Data System (ADS)

Özdemir, Yavuz; Mercan, Çaǧrı; Oyan, Vural; Atakul-Özdemir, Ayşe

2017-04-01

The Eastern Anatolian Cenozoic continental intraplate volcanism was initiated in Middle Miocene as a result of the convergence between the Arabian and Anatolian plates. The origin of Eastern Anatolian volcanism has been the focus of many petrological studies that have aimed to resolve the relative contributions of asthenospheric mantle and/or lithospheric mantle with/without subduction component in the genesis of magmas that compositionally have many affinities to ocean island basalts (OIB) and volcanic arcs. Volcanism in the region characterized by mainly stratovolcanoes, basaltic lava plateaus and are dominantly spread at the northern parts of Bitlis Pötürge Massif (BPM). Our study focuses on a small scale Quaternary basaltic system that firstly observed within the BPM. The volcanic rocks of our study located 50 km to the south of Lake Van and are basanitic in composition. They exposed along K-G striking tensional fissures and crosscut the Upper unit of the Bitlis Massif. Initial products of the volcanism are scoria fall deposits. Thick basanitic lava flows overly the pyroclastics and formed columnar structures. The basanites are generally fine-grained with phenocrysts of olivine+clinopyroxene. The groundmass is typically of clinopyroxene, olivine and Ti magnetite and Cr spinel with interstitial nepheline. The olivine phenocrysts are typically euhedral to subhedral with Forsterite contents of Fo73-83. Clinopyroxenes are highly calcic and show modest variations in Wo47-52-En34-42-Fs10-15 and are weakly zoned with mg# 89-87 at cores to 86-84 at rims. Nephelines occur as minor minerals within the networks of other groundmass minerals. Ti rich and Fe-Cr spinels occur as inclusions in olivine and clinopyroxenes as well as within the groundmass. LILE and LREE enrichments over HFSE and HREE suggest similarities with magmas generated from enriched mantle sources. EC-AFC modeling of trace element and isotope compositions indicates that assimilation of crustal lithologies have minor effect on the evolutionary stages of basanitic rocks. Based on LREE/HREE, MREE/HREE ratios and partial melting models, we suggest that basanitic rocks of Çatak are produced from a lower degree melting of a garnet bearing mantle source.

Geochemical constraints on genesis of Paleoproterozoic A-type granite in the south margin of North China Craton

NASA Astrophysics Data System (ADS)

Xue, Shuo; Xu, Yang; Ling, Ming-Xing; Kang, Qing-Qing; Jiang, Xiao-Yan; Sun, Sai-Jun; Wu, Kai; Zhang, Zhe-Kun; Luo, Ze-Bin; Liu, Yu-Long; Sun, Weidong

2018-04-01

Paleoproterozoic A-type granites are widely outcropped in the North China Craton (NCC), particularly in the Trans-North China Orogen. However, their genesis and tectonic significance remain obscure. Here we report systematic studies on geochronology and geochemical characteristics of A-type granite in Huayangchuan, south margin of the NCC. The samples are enriched in total alkali (K2O + Na2O > 8.97 wt%), and depleted in MgO (0.84-0.93 wt%), CaO (1.28-1.90 wt%) and P2O5 (0.18-0.20 wt%), with high FeOT/MgO (5.69-6.67). They are characterized by high Zr + Y + Nb + Ce values (1293-1392 ppm) and 10,000 × Ga/Al ratios (3.14-3.35), which are typical characteristics of A-type granite. The Huayangchuan A-type granite can be further classified as A1-type subgroup based on particular geochemical features, e.g., low Y/Nb (0.87-1.00) and Yb/Ta (0.88-1.10). High precision zircon U-Pb dating of the A-type granite by secondary ion mass spectrometry (SIMS) yields Paleoproterozoic 207Pb/206Pb ages of 1829.5 ± 2.5 Ma. The low zircon ɛHf(t) values (-6.97 to -10.45), along with zircon Hf model age of 2.7-2.9 Ga, indicate that the Huayangchuan A-type granite was derived from partial melting of the ancient continental crust with contribution of enriched mantle components. The low zircon δ18O composition (4.00 to 6.78‰) indicates that the zircons were crystallized from low δ18O magmas, which derived from the crust metasomatized by low δ18O mantle fluids or melts. The E-W trend A1-type granitic plutons in the NCC are generally outcropped in a rift tectonic regime, which is consistent with the development of the mantle plume in the Xiong'er district. The large volume of basaltic magmas, generated by mantle plume head, underplated the lower continental crust and formed the Huayangchuan A-type granite.

The mantle source of island arc magmatism during early subduction: Evidence from Hf isotopes in rutile from the Jijal Complex (Kohistan arc, Pakistan)

NASA Astrophysics Data System (ADS)

Ewing, Tanya A.; Müntener, Othmar

2018-05-01

The Cretaceous-Paleogene Kohistan arc complex, northern Pakistan, is renowned as one of the most complete sections through a preserved paleo-island arc. The Jijal Complex represents a fragment of the plutonic roots of the Kohistan arc, formed during its early intraoceanic history. We present the first Hf isotope determinations for the Jijal Complex, made on rutile from garnet gabbros. These lithologies are zircon-free, but contain rutile that formed as an early phase. Recent developments in analytical capabilities coupled with a careful analytical and data reduction protocol allow the accurate determination of Hf isotope composition for rutile with <30 ppm Hf for the first time. Rutile from the analysed samples contains 5-35 ppm Hf, with sample averages of 13-17 ppm. Rutile from five samples from the Jijal Complex mafic section, sampling 2 km of former crustal thickness, gave indistinguishable Hf isotope compositions with εHf(i) ranging from 11.4 ± 3.2 to 20.1 ± 5.7. These values are within error of or only slightly more enriched than modern depleted mantle. The analysed samples record variable degrees of interaction with late-stage melt segregations, which produced symplectitic overprints on the main mineral assemblage as well as pegmatitic segregations of hydrous minerals. The indistinguishable εHf(i) across this range of lithologies demonstrates the robust preservation of the Hf isotope composition of rutile. The Hf isotope data, combined with previously published Nd isotope data for the Jijal Complex garnet gabbros, favour derivation from an inherently enriched, Indian Ocean type mantle. This implies a smaller contribution from subducted sediments than if the source was a normal (Pacific-type) depleted mantle. The Jijal Complex thus had only a limited recycled continental crustal component in its source, and represents a largely juvenile addition of new continental crust during the early phases of intraoceanic magmatism. The ability to determine the Hf isotope composition of rutile with low Hf contents is an important development for zircon-free mafic lithologies. This study highlights the potential of Hf isotope analysis of rutile to characterise the most juvenile deep arc crust cumulates worldwide.

Mix or un-mix? Trace element segregation from a heterogeneous mantle, simulated.

NASA Astrophysics Data System (ADS)

Katz, R. F.; Keller, T.; Warren, J. M.; Manley, G.

2016-12-01

Incompatible trace-element concentrations vary in mid-ocean ridge lavas and melt inclusions by an order of magnitude or more, even in samples from the same location. This variability has been attributed to channelised melt flow [Spiegelman & Kelemen, 2003], which brings enriched, low-degree melts to the surface in relative isolation from depleted inter-channel melts. We re-examine this hypothesis using a new melting-column model that incorporates mantle volatiles [Keller & Katz 2016]. Volatiles cause a deeper onset of channelisation: their corrosivity is maximum at the base of the silicate melting regime. We consider how source heterogeneity and melt transport shape trace-element concentrations in basaltic lavas. We use both equilibrium and non-equilibrium formulations [Spiegelman 1996]. In particular, we evaluate the effect of melt transport on probability distributions of trace element concentration, comparing the inflow distribution in the mantle with the outflow distribution in the magma. Which features of melt transport preserve, erase or overprint input correlations between elements? To address this we consider various hypotheses about mantle heterogeneity, allowing for spatial structure in major components, volatiles and trace elements. Of interest are the roles of wavelength, amplitude, and correlation of heterogeneity fields. To investigate how different modes of melt transport affect input distributions, we compare melting models that produce either shallow or deep channelisation, or none at all.References:Keller & Katz (2016). The Role of Volatiles in Reactive Melt Transport in the Asthenosphere. Journal of Petrology, http://doi.org/10.1093/petrology/egw030. Spiegelman (1996). Geochemical consequences of melt transport in 2-D: The sensitivity of trace elements to mantle dynamics. Earth and Planetary Science Letters, 139, 115-132. Spiegelman & Kelemen (2003). Extreme chemical variability as a consequence of channelized melt transport. Geochemistry Geophysics Geosystems, http://doi.org/10.1029/2002GC000336

Enriched continental flood basalts from depleted mantle melts: modeling the lithospheric contamination of Karoo lavas from Antarctica

NASA Astrophysics Data System (ADS)

Heinonen, Jussi S.; Luttinen, Arto V.; Bohrson, Wendy A.

2016-01-01

Continental flood basalts (CFBs) represent large-scale melting events in the Earth's upper mantle and show considerable geochemical heterogeneity that is typically linked to substantial contribution from underlying continental lithosphere. Large-scale partial melting of the cold subcontinental lithospheric mantle and the large amounts of crustal contamination suggested by traditional binary mixing or assimilation-fractional crystallization models are difficult to reconcile with the thermal and compositional characteristics of continental lithosphere, however. The well-exposed CFBs of Vestfjella, western Dronning Maud Land, Antarctica, belong to the Jurassic Karoo large igneous province and provide a prime locality to quantify mass contributions of lithospheric and sublithospheric sources for two reasons: (1) recently discovered CFB dikes show isotopic characteristics akin to mid-ocean ridge basalts, and thus help to constrain asthenospheric parental melt compositions and (2) the well-exposed basaltic lavas have been divided into four different geochemical magma types that exhibit considerable trace element and radiogenic isotope heterogeneity (e.g., initial ɛ Nd from -16 to +2 at 180 Ma). We simulate the geochemical evolution of Vestfjella CFBs using (1) energy-constrained assimilation-fractional crystallization equations that account for heating and partial melting of crustal wall rock and (2) assimilation-fractional crystallization equations for lithospheric mantle contamination by using highly alkaline continental volcanic rocks (i.e., partial melts of mantle lithosphere) as contaminants. Calculations indicate that the different magma types can be produced by just minor (1-15 wt%) contamination of asthenospheric parental magmas by melts from variable lithospheric reservoirs. Our models imply that the role of continental lithosphere as a CFB source component or contaminant may have been overestimated in many cases. Thus, CFBs may represent major juvenile crustal growth events rather than just recycling of old lithospheric materials.

Abnormal Elasticity of Single-Crystal Magnesiosiderite across the Spin Transition in Earth's Lower Mantle

NASA Astrophysics Data System (ADS)

Fu, S.; Yang, J.; Lin, J. F.

2016-12-01

Carbon can be transported into deep Earth's interior via subduction of carbonated oceanic crust, hosted as Mg-Fe bearing carbonates. The existence of stable carbonate can significantly affect our understanding on geochemical and geophysical properties of the planet. Early studies have shown that iron spin-pairing transition could occur in the iron-enriched carbonates, generally called magnesiosiderite, under lower mantle conditions. The pressure-induced spin state change is accompanied by a sudden volume collaps. However, the effects of the spin-pairing transition on single-crystal elasticity of magnesiosiderite under high pressure conditions are still unclear. Understanding the elasticity of single-crystal magnesiosiderite at relevant lower mantle conditions plays an important role in better understanding the seismic signatures in the carbon-enriched region, and to constrain carbon storage and recycling in the mantle. In order to solve all individual elastic constants (C11, C22, C33, C44, C55, C66, C12, C23, and C13) of magnesiosiderite at high pressures via Christoffel's equations, we employed Brillouin Light Scattering (BLS) to measure shear wave (Vs) and compressional wave velocities (Vp) as a function of the azimuthal angle under lower mantle pressures, accompanied by Impulsive Stimulate Light Scattering (ISS) to measure the Vp when pressures are too high to measure it by BLS. A general thermoelastic modelling was developed to fit the elastic softening within the spin transition. We will further discuss the effects of pressures, as well as iron spin states, on the single-crystal elasticity and seismic parameters (Vp and Vs anisotropy AVp, AVs, etc) at lower mantle conditions. These results could provide clues in explaining regional seismic heterogeneities in deep mantle.

Subduction-related cryptic metasomatism in fore-arc to nascent fore-arc Neoproterozoic mantle peridotites beneath the Eastern Desert of Egypt: mineral chemical and geochemical evidences

NASA Astrophysics Data System (ADS)

Hamdy, Mohamed; Salam Abu El-Ela, Abdel; Hassan, Adel; Kill, Youngwoo; Gamal El Dien, Hamed

2013-04-01

Mantle spinel peridotites beneath the Arabian Nubian Shield (ANS) in the Eastern Desert (ED) of Egypt were formed in arc stage in different tectonic setting. Thus they might subject to exchange with the crustal material derived from recycling subducting oceanic lithosphere. This caused metasomatism enriching the rocks in incompatible elements and forming non-residual minerals. Herein, we present mineral chemical and geochemical data of four ophiolitic mantle slice serpentinized peridotites (W. Mubarak, G. El-Maiyit, W. Um El Saneyat and W. Atalla) widely distributed in the ED. These rocks are highly serpentinized, except some samples from W. Mubarak and Um El-Saneyat, which contain primary olivine (Fo# = 90-92 mol %) and orthopyroxene (En# = 86-92 mol %) relics. They have harzburgite composition. Based on the Cr# and Mg# of the unaltered spinel cores, all rocks formed in oceanic mantle wedge in the fore-arc setting, except those from W. Atalla formed in nascent fore-arc. This implies that the polarity of the subduction during the arc stage was from the west to the east. These rocks are restites formed after partial melting between 16.58 in W. Atalla to 24 % in G-El Maiyit. Melt extraction occurred under oxidizing conditions in peridotites from W. Mubarak and W. Atalla and under reducing conditions in peridotites from G. El-Maiyit and Um El-Saneyat. Cryptic metasomatism in the studied mantle slice peridotites is evident. This includes enrichment in incompatible elements in minerals and whole rocks if compared with the primitive mantle (PM) composition and the trend of the depletion in melt. In opx the Mg# doesn't correlate with TiO2, CaO, MnO, NiO and Cr2O3concentrations. In addition, in serpentinites from W. Mubarak and W. Atalla, the TiO2spinel is positively correlated with the TiO2 whole-rock, proposing enrichment by the infiltration of Ti-rich melts, while in G. El- Maiyit and Um El-Saneyat serpentinites they are negatively correlated pointing to the reaction with the Ti-rich melts. All rocks are enriched LREE, FMEs and HFSEs. This took place mostly by different agents. As the H2O-rich liquid, which seems to have been produced from the subducting oceanic slab percolating peridotites, gradually loses trace elements, the HFSEs are fractionated from LILEs and REEs. This could explain the high ratios of (Nb/La)N and (Nb/Ba)N of some of the studied rocks. All the studied serpentinized mantle slices have subchonddritic to near chondritic ratios of Nb/Ta (< 13.8) and Zr/ Hf (< 36.09). It is suggested that Nb did not fractionate from Ta and Zr from Hf. There are might be silicate melts enriched the peridotites in Ta rather than Nb causing a much great decrease in the Nb/Ta especially serpentinites from W. Mubarak. This melt/fluid might have been derived from recycled subducted oceanic crust or from hot asthenosphere. Concentrations of U in all the studied samples (except for W. Mubarak serpentinites) are positively correlated with LILEs, Pb and Mo, indicating that the studied serpentinites were enriched in these elements from the same fluids, most probably derived from subducted oceanic lithosphere. Positive anomalies of Li (in W. Mubarak and G. El-Maiyit serpentinites), U (except for W. Mubarak serpentinites), Mo and Pb are characteristics of hydrothermally altered ocean-floor peridotites. High Sr/Nd ratios may be typical of the hydrous metasomatism caused by hydrous melt/fluid.

Stability of iron-rich magnesiowüstite in Earth's lower mantle

NASA Astrophysics Data System (ADS)

Ohta, K.; Fujino, K.; Kuwayama, Y.; Kondo, T.; Shimizu, K.; Ohishi, Y.

2012-12-01

At ambient conditions, MgO periclase and FeO wüstite form a solid solution (Mg1-xFex)O, named ferropericlase (x ≤ 0.5) and magnesiowüstite (x > 0.5). (Mg1-xFex)O ferropericlase is considered to be a major component of Earth's lower mantle, and may play an important role for its structure and dynamics. Iron-rich magnesiowüstite also needs to be considered because of possible iron enrichment at the core-mantle boundary region [e.g., Nomura et al., 2011]. Recent laser-heated diamond anvil cell experiments on FeO revealed that NaCl-type (B1) structured FeO underwent an insulator-metal transition at about 70 GPa and 1800 K without any structural transformation [Fischer et al., 2011; Ohta et al., 2012]. These results imply that the metallic B1 FeO would require a two-phase field for the MgO-FeO binary system due to different chemical bonding between insulating MgO and metallic FeO. We performed simultaneous electrical conductivity and x-ray diffraction measurements on (Mg0.20Fe0.80)O and (Mg0.05Fe0.95)O magnesiowüstite up to 140 GPa and 2100 K, and then examined recovered samples by using analytical transmission electron microprobe. We obtained some evidences for the dissociation of (Mg0.05Fe0.95)O into lighter and heavier phases than starting material occurring above 70 GPa and 1900 K, which is most likely due to the metallization of FeO component. On the other hand, we did not observe such dissociation and metallization in (Mg0.20Fe0.80)O. Observed dissociation in (Mg0.05Fe0.95)O might contribute to the heterogeneity in seismic wave and electrical conductivity at the Earth's core-mantle boundary region.

The geology and geochemistry of Isla Floreana, Galápagos: A different type of late-stage ocean island volcanism: Chapter 6 in The Galápagos: A natural laboratory for the earth sciences

USGS Publications Warehouse

Harpp, Karen S.; Geist, Dennis J.; Koleszar, Alison M.; Christensen, Branden; Lyons, John; Sabga, Melissa; Rollins, Nathan; Harpp, Karen S.; Mittelstaedt, Eric; d'Ozouville, Noémi; Graham, David W

2014-01-01

Isla Floreana, the southernmost volcano in the Galápagos Archipelago, has erupted a diverse suite of alkaline basalts continually since 1.5 Ma. Because these basalts have different compositions than xenoliths and older lavas from the deep submarine sector of the volcano, Floreana is interpreted as being in a rejuvenescent or late-stage phase of volcanism. Most lavas contain xenoliths, or their disaggregated remains. The xenolithic debris and large ranges in composition, including during single eruptions, indicate that the magmas do not reside in crustal magma chambers, unlike magmas in the western Galápagos. Floreana lavas have distinctive trace element compositions that are rich in fluid-immobile elements (e.g., Ta, Nb, Th, Zr) and even richer in fluid-mobile elements (e.g., Ba, Sr, Pb). Rare earth element (REE) patterns are light REE-enriched and distinctively concave-up. Neodymium isotopic ratios are comparable to those from Fernandina, at the core of the Galápagos plume, but Floreana has the most radiogenic Sr and Pb isotopic ratios in the archipelago. These trace element patterns and isotopic ratios are attributed to a mixed source originating within the Galápagos plume, which includes depleted upper mantle, plume material rich in TITAN elements (Ti, Ta, Nb), and recycled oceanic crust that has undergone partial dehydration in an ancient subduction zone. Because Floreana lies at the periphery of the Galápagos plume, melting occurs mostly in the spinel zone, and enriched components dominate; the Floreana recycled mantle component influence is detectable in volcanoes along the entire southern periphery of the archipelago as well. Floreana is the only Galápagos volcano known to have undergone late-stage volcanism. Here, however, the secondary stage activity is more compositionally enriched than the shield-building phase, in contrast to what is observed in Hawai‘i, suggesting that the mechanism driving late-stage volcanism may vary among ocean island provinces.

Trace element distribution in peridotite xenoliths from Tok, SE Siberian craton: A record of pervasive, multi-stage metasomatism in shallow refractory mantle

NASA Astrophysics Data System (ADS)

Ionov, Dmitri A.; Chazot, Gilles; Chauvel, Catherine; Merlet, Claude; Bodinier, Jean-Louis

2006-03-01

Spinel peridotite xenoliths in alkali basalts at Tok, SE Siberian craton range from fertile lherzolites to harzburgites and wehrlites; olivine-rich (70-84%) rocks are dominant. REE patterns in the lherzolites range from nearly flat for fertile rocks (14-17% cpx) to LREE-enriched; the enrichments are positively correlated with modal olivine, consistent with high-permeability of olivine-rich rocks during melt percolation. Clinopyroxene in olivine-rich Tok peridotites typically has convex-upward trace element patterns (La/Nd PM < 1 and Nd/Yb PM ≫ 1), which we consider as evidence for equilibration with evolved silicate liquids (with higher REE and lower Ti contents than in host basalts). Whole-rock patterns of the olivine-rich xenoliths range from convex-upward to LREE-enriched (La/Nd PM > 1); the LREE-enrichments are positively correlated with phosphorus abundances and are mainly hosted by accessory phosphates and P-rich cryptocrystalline materials. In addition to apatite, some Tok xenoliths contain whitlockite (an anhydrous, halogen-poor and Na-Mg-rich phosphate), which is common in meteorites and lunar rocks, but has not been reported from any terrestrial mantle samples. Some olivine-rich peridotites have generations of clinopyroxene with distinct abundances of Na, LREE, Sr and Zr. The mineralogical and trace element data indicate that the lithospheric mantle section represented by the xenoliths experienced a large-scale metasomatic event produced by upward migration of mafic silicate melts followed by percolation of low- T, alkali-rich melts and fluids. Chromatographic fractionation and fractional crystallisation of the melts close to the percolation front produced strong LREE-enrichments, which are most common in the uppermost mantle and are related to carbonate- and P 2O 5-rich derivatives of the initial melt. Reversal and gradual retreat of the percolation front during thermal relaxation to ambient geotherm ("retrograde" metasomatism) caused local migration and entrapment of small-volume residual fluids and precipitation of volatile-rich accessory minerals. A distinct metasomatic episode, which mainly produced "anhydrous" late-stage interstitial materials was concomitant with the alkali basaltic magmatism, which brought the xenoliths to the surface.

Between carbonatite and lamproite—Diamondiferous Torngat ultramafic lamprophyres formed by carbonate-fluxed melting of cratonic MARID-type metasomes

NASA Astrophysics Data System (ADS)

Tappe, Sebastian; Foley, Stephen F.; Kjarsgaard, Bruce A.; Romer, Rolf L.; Heaman, Larry M.; Stracke, Andreas; Jenner, George A.

2008-07-01

New U-Pb perovskite ages reveal that diamondiferous ultramafic lamprophyre magmas erupted through the Archean crust of northern Labrador and Quebec (eastern Canada) between ca. 610 and 565 Ma, a period of strong rifting activity throughout contiguous Laurentia and Baltica. The observed Torngat carbonate-rich aillikite/carbonatite and carbonate-poor mela-aillikite dyke varieties show a large spread in Sr-Nd-Hf-Pb isotope ratios with pronounced correlations between isotope systems. An isotopically depleted component is identified solely within aillikites ( 87Sr/ 86Sr i = 0.70323-0.70377; ɛNd i = +1.2-+1.8; ɛHf i = +1.4-+3.5; 206Pb/ 204Pb i = 18.2-18.5), whereas some aillikites and all mela-aillikites range to more enriched isotope signatures ( 87Sr/ 86Sr i = 0.70388-0.70523; ɛNd i = -0.5 to -3.9; ɛHf i = -0.6 to -6.0; 206Pb/ 204Pb i = 17.8-18.2). These contrasting isotopic characteristics of aillikites/carbonatites and mela-aillikites, along with subtle differences in their modal carbonate, SiO 2, Al 2O 3, Na 2O, Cs-Rb, and Zr-Hf contents, are consistent with two distinctive metasomatic assemblages of different age in the mantle magma source region. Integration of petrologic, geochemical, and isotopic information leads us to propose that the isotopically enriched component originated from a reduced phlogopite-richterite-Ti-oxide dominated source assemblage that is reminiscent of MARID suite xenoliths. In contrast, the isotopically depleted component was derived from a more oxidized phlogopite-carbonate dominated source assemblage. We argue that low-degree CO 2-rich potassic silicate melts from the convective upper mantle were preferentially channelled into an older, pre-existing MARID-type vein network at the base of the North Atlantic craton lithosphere, where they froze to form new phlogopite-carbonate dominated veins. Continued stretching and thinning of the cratonic lithosphere during the Late Neoproterozoic remobilized the carbonate-rich vein material and induced volatile-fluxed fusion of the MARID-type veins and the cold peridotite substrate. Isotopic modelling suggests that only 5-12% trace element contribution from such geochemically extreme MARID-type material is required to produce the observed compositional shift from the isotopically most depleted aillikites/carbonatites towards enriched mela-aillikites. We conclude that cold cratonic mantle lithosphere can host several generations of contrasting vein assemblages, and that each may have formed during past tectonic and magmatic events under distinctively different physicochemical conditions. Although cratonic MARID-type and carbonate-bearing veins in peridotite can be the respective sources for lamproite and carbonatite magmas when present as the sole metasome, their concomitant fusion in a complex source region may give rise to a whole new variety of deep volatile-rich magmas and we suggest that orangeites (formerly Group 2 kimberlites), kamafugites, and certain types of ultramafic lamprophyre are formed in this manner.

Production of mildly alkaline basalts at complex ocean ridge settings: Perspectives from basalts emitted during the 2010 eruption at the Eyjafjallajökull volcano, Iceland

NASA Astrophysics Data System (ADS)

Viccaro, Marco; Nicotra, Eugenio; Urso, Salvatore

2015-11-01

The early phase of the 2010 eruption at the Eyjafjallajökull volcano (Iceland) produced poorly evolved mildly alkaline basalts that have a signature more enriched with respect to the typically depleted basalts emitted at ocean ridges. The whole rock geochemistry of these basaltic magmas offers a great opportunity to investigate the mantle source characteristics and reasons leading to this enriched fingerprint in proximity of the ocean ridge system. Some basaltic products of Katla volcano, ∼25 km east of Eyjafjallajökull, have been chosen from the literature, as they display a similar mildly alkaline signature and can be therefore useful to explore the same target. Major and trace element variations of the whole rock suggest a very limited evolutionary degree for the 2010 Eyjafjallajökull products and the selected Katla magmas, highlighting the minor role played by differentiation processes such as fractional crystallization. Nevertheless, effects of the limited fractionation have been erased through re-equilibration of the major and trace element abundances at primary conditions. Concentrations of Th after re-equilibration have been assumed as indexes of the partial melting degree, given the high incompatibility of the element, and enrichment ratios calculated for each trace element. Especially for LILE (Rb, Ba, K, Sr), the pattern of resulting enrichment ratios well matches that obtained from fractional melting of peridotite bearing hydrous phases (amphibole/phlogopite). This put forward the idea that magmas have been generated through partial melting of enriched mantle domains where hydrous minerals have been stabilized as a consequence of metasomatic processes. Refertilization of the mantle has been attributed to intrusion of hydrous silicate melts and fractional crystallization of hydrous cumulates. These refertilizing melts, inherited from an ancient subducted oceanic crust, intruded into a depleted oceanic lithosphere that remained stored for a long time (hundreds of Ma or Ga) before being re-entrained in partial melting. This means that magmas could have acquired their main geochemical differences in response of the variable depletion/enrichment degree of the heterogeneous mantle portion tapped at rather shallow depth (≤100 km). Our finding is another tessera in the open debate on the plume-related vs. non plume-related origin of Icelandic magmatism.

Les xénolites ultramafiques du volcanisme alcalin quaternaire d'Oranie (Tell, Algérie occidentale), témoins d'une lithosphère cisaillée et enrichieUltramafic xenoliths from Quaternary alkali volcanism from Oranie (Tell, western Algeria): witnesses of a sheared and enriched lithosphere

NASA Astrophysics Data System (ADS)

Zerka, Mohamed; Cottin, Jean-Yves; Grégoire, Michel; Lorand, Jean-Pierre; Megartsi, M'Hamed; Midoun, Mohamed

Numerous ultramafic xenoliths occur within the Aı̈n-Temouchent volcanic complex (Northwestern Oranie, Algeria). Most of them are type I mantle tectonites (lherzolites and harzburgites) and composite xenoliths (harzburgite/clinopyroxenite) are rare. Only a few samples of spinel lherzolites display relatively fertile compositions when the major part of type I xenoliths have refractory major element compositions but enriched LREE contents showing that they have been affected by mantle metasomatism. The composite xenoliths are witnesses of reactions of alkaline magmas with the upper mantle. An asthenospheric rising, in relation with the large strike slip fault affecting the North African plate margin at Trias time is proposed as a possible geodynamical setting. To cite this article: M. Zerka et al., C. R. Geoscience 334 (2002) 387-394.

Sodium Inverse Relationships During Melting in Ultraslow Spreading Regions: Insights from SWIR-Smoothseafloor Peridotites

NASA Astrophysics Data System (ADS)

Cannat, M.; Brunelli, D.; Paquet, M.; Sforna, M. C.; Seyler, M.

2015-12-01

Ultraslow spreading ridges are key regions to unravel mantle processes. Low potential temperatures and reduced melting allow decrypting early melting processes and shad lights on the source short-scale heterogeneities and their interactions with transient melts. Mantle-derived peridotites from the Smoothseafloor region of the eastern Southwest Indian Ridge reveal countertrending Na-Ti relationships. Na apparently behaves as a compatible element during partial melting similarly to light REEs. Heavy REEs, however, follow a normal relationship with the other melting indicators (e.g. Cr#), a behaviour that results in pattern rotation around a pivot element when looking to REE systematic. These relationships can be explained by percolation of relatively enriched, grt-field derived, melts in the spinel-field melting mantle 1. A feature that also explains the inverse Na-Cr# correlation, frequently observed in abyssal mantle rocks. Experimental relationships constraint the grt-field derived melts to be produced by low-melting paragenesis that experience a garnet to spinel phase transition shallower than mantle peridotites for a given temperature. Based on potential mantle temperatures estimated by Cannat et al., 19992, the grt-sp transition can be set at ca. 2.0 and 1.5 GPa for mantle peridotites and Mg pyroxenites respectively with the onset of mantle melting at 1.2 GPa. Mass balance calculations based on the amount of produced melt constrains the pyroxenitic fraction < 10% by mass of the mantle source. The contemporaneous presence of lithologies too depleted with respect to the described process suggests that some portions of the mantle source are inherited from more sustained ancient depletion events not related to present-day processes beneath this ridge portion. PNRA funding : PdR 2013/B1.02 1. Brunelli, D., et al., 2104. Percolation of enriched melts during incremental open-system melting in the spinel field : A REE approach to abyssal peridotites from the Southwest Indian Ridge. Geochim. Cosmochim. Acta 127,190-203. 2. Cannat, M., et al., 1999. Formation of the axial relief at the very slow spreading Southwest Indian Ridge (49° to 69°E). J. Geophys. Res. 104, 22825-22843.

Microscale Variations in the 13C Content of the Murchison Meteorite

NASA Astrophysics Data System (ADS)

Romanek, C.; Gibson, E.; Socki, R.; Burkett, P. J.

1993-07-01

Heretofore unresolved micrometer-scale carbon isotopic zonation in the Murchison meteorite (CM3) is documented using a laser microprobe mass spectrometer. High-resolution isotopic gradients and heterogeneities between high- and low-temperature textural components help to constrain the processes that have shaped the physiochemical character of this carbonaceous chondrite. Previous bulk samples of Murchison yield an average delta ^13C value of - 5.7 +/- 4.3 per mil [1] while individual components such as micrometer-sized mineral separates (e.g., C(sub)graphite , C(sub)diamond, and SiC), acid- soluble extracts (e.g., CaCO3 and polar hydrocarbons), and insoluble residues (e.g., polycyclic aromatic hydrocarbons) are isotopically diverse (delta ^13C of -1000 to 29,000 per mil). While these studies shed light on the origin and occurrence of C-bearing phases, they fail to constrain intrinsic spatial isotopic heterogeneities. The power of the laser microprobe lies in the fact that in situ chemical and isotopic compositions are measured simultaneously for volatiles extracted from extremely small sample volumes (i.e., 0.025 mm^3 for 5 wt% C). Nd-YAG laser irradiation (1.06 micrometers) is directed onto texturally defined targets (>=50 micrometers wide) from which solid material is volatilized. Condensible gaseous phases are collected in a variable-temperature cold trap while the more volatile species (CH4 and CO) are quantified using an ion trap mass spectrometer. All gases are then converted to CO2 in a CuO furnace (containing Pt) held at 600 degrees C and analyzed for carbon and oxygen isotope ratios. The concentration and isotopic composition of condensed species are determined by stepped sublimation of unstable components and conversion to CO2. Preliminary isotopic analyses of the total volatile C content (i.e., bulk microanalysis) from distinct textural components at least 0.05 mm^3 in volume are described below. The most ^13C-depleted components within Murchison reside within the cores of chondrules and/or aggregates. Three typical cores were analyzed, with an average bulk composition of -21.0 +/- 0.5 per mil (n = 7). The bulk ^13C content of C-bearing phases increases monotonically outward in all directions within 100 to 200 micrometers of each core (i.e., within dust mantles) to a constant matrix value of -12.5 +/- 0.5 per mil (n = 40). The most isotopically enriched textural component found in Murchison is a regolith breccia clast without chondrules that has an average bulk delta ^13C value of -10 +/-0.5 per mil (n = 5). The clast was originally detectable only under cathodoluminescence, but with the aid of the laser microprobe it is now characterized by an unusually low volatile content and enriched ^13C composition. In general, the most isotopically enriched components also produce the lowest yield of gas (normalized to sampling volume). This trend of isotopic enrichment from chondrule to matrix has been documented previously for oxygen isotopes in carbonaceous chondrites [2]. Carbon isotopic gradients and heterogeneities within Murchison reflect fundamental changes in the chemical speciation and/or isotopic content of the main C-bearing components (i.e., acid-soluble and insoluble hydrocarbon fractions) within the meteorite. Perhaps core interiors and dust mantles are responding to environmental changes reflected in the speciation of C-bearing species distributed within the solar nebula or the parent body. Inverse correlations between hydrocarbon atomic mass number and ^13C abundance in the acid-soluble [3] and insoluble residues [4] of Murchison have been documented. Alternatively, micrometer-scale isotopic gradients may reflect fundamental changes in the isotopic composition of individual C-bearing species through time. Enrichments may represent kinetically controlled processes related to hydrocarbon formation. In contrast, assuming an equilibrium fractionation mechanism, isotopic enrichments may record a temperature-dependent component to hydrocarbon delta ^13C values. These opposing alternatives will be discussed in light of the isotopic composition of individual C-bearing components volatilized from tightly constrained sample volumes within Murchison. References: [1] Kerridge J. F. (1985) GCA, 49, 1707-1714. [2] Clayton R. N. and Mayeda T. K. (1984) EPSL, 67, 151-161. [3] Yuen G. et al. (1984) Nature, 307, 254. [4] Gilmour I. et al. (1991) Meteoritics, 26, 337-338.

Decoupling of Mg-C and Sr-Nd-O isotopes traces the role of recycled carbon in magnesiocarbonatites from the Tarim Large Igneous Province

NASA Astrophysics Data System (ADS)

Cheng, Zhiguo; Zhang, Zhaochong; Hou, Tong; Santosh, M.; Chen, Lili; Ke, Shan; Xu, Lijuan

2017-04-01

The Tarim Large Igneous Province in NW China hosts numerous magmatic carbonatite dikes along its northern margin. The carbonatites are composed mainly of dolomite (90 vol.%) and minor calcite (5 vol.%), with apatite, barite, celestine, aegirine, monazite and bastnaesite as accessory minerals. The rocks correspond to magnesiocarbonatites with a compositional range of 13.73-19.59 wt.% MgO, and 20.03-30.11 wt.% CaO, along with 1.65-3.31 wt.% total Fe2O3, 0.02-2.39 wt.% SiO2 and other minor elements, such as P2O5, Na2O and K2O. These magnesiocarbonatites are characterized by extreme enrichment in incompatible elements with high total rare earth element (REE) contents of 372-36965 ppm. The strontium [(87Sr/86Sr)i = 0.70378-0.70386], neodymium [εNd(t) = +2.51 - +3.59] and oxygen (δ18OV-SMOW = 5.9‰-8.0‰) isotope values of these rocks are consistent with a mantle origin, whereas the magnesium (δ26Mg = -1.09‰ to -0.85‰) and carbon (δ13CV-PDB = -4.1‰ to -5.9‰) isotopes are decoupled from mantle values and reflect signature of recycled sedimentary carbonates. Global plate tectonic models predict that sedimentary carbonates in convergent margins are subducted to deep domains in the mantle, with phase transitions from calcite/dolomite to magnesite, and eventually to periclase/perovskite. The involvement of a mantle plume enhances the normal mantle geotherms and promotes decomposition reactions of magnesite. The decoupling of Mg-C and Sr-Nd-O isotopes in the mangesiocarbonatites provides insights on the origin of carbonatites, and also illustrates a case of interaction between mantle plume and subduction-related components.

The effects of magmatic processes and crustal recycling on the molybdenum stable isotopic composition of Mid-Ocean Ridge Basalts

NASA Astrophysics Data System (ADS)

Bezard, Rachel; Fischer-Gödde, Mario; Hamelin, Cédric; Brennecka, Gregory A.; Kleine, Thorsten

2016-11-01

Molybdenum (Mo) stable isotopes hold great potential to investigate the processes involved in planetary formation and differentiation. However their use is currently hampered by the lack of understanding of the dominant controls driving mass-dependent fractionations at high temperature. Here we investigate the role of magmatic processes and mantle source heterogeneities on the Mo isotope composition of Mid-Ocean Ridges Basalts (MORBs) using samples from two contrasting ridge segments: (1) the extremely fast spreading Pacific-Antarctic (66-41°S) section devoid of plume influence and; (2) the slow spreading Mohns-Knipovich segment (77-71°N) intercepted by the Jan Mayen Plume (71°N). We show that significant variations in Mo stable isotope composition exist in MORBs with δ98/95Mo ranging from - 0.24 ‰ to + 0.15 ‰ (relative to NIST SRM3134). The absence of correlation between δ98/95Mo and indices of magma differentiation or partial melting suggests a negligible impact of these processes on the isotopic variations observed. On the other hand, the δ98/95Mo variations seem to be associated with changes in radiogenic isotope signatures and rare earth element ratios (e.g., (La/Sm)N), suggesting mantle source heterogeneities as a dominant factor for the δ98/95Mo variations amongst MORBs. The heaviest Mo isotope compositions correspond to the most enriched signatures, suggesting that recycled crustal components are isotopically heavy compared to the uncontaminated depleted mantle. The uncontaminated depleted mantle shows slightly sub-chondritic δ98/95Mo, which cannot be produced by core formation and, therefore, more likely result from extensive anterior partial melting of the mantle. Consequently, the primitive δ98/95Mo composition of the depleted mantle appears overprinted by the effects of both partial melting and crustal recycling.

Food-web dynamics and trophic-level interactions in a multispecies community of freshwater unionids

USGS Publications Warehouse

Nichols, S.J.; Garling, D.

2000-01-01

We compared feeding habits and trophic-level relationships of unionid species in a detritus-dominated river and an alga-dominated lake using biochemical analyses, gut contents, and stable-isotope ratios. The δ13C ratios for algae and other food-web components show that all unionids from both the river and the lake used bacterial carbons, not algal carbons, as their main dietary source, in spite of positive selection and concentration of diatoms and green algae from the water column in the gut and mantle cavity. Algae did provide key nutrients such as vitamins A and D and phytosterols that were bioaccumulated in the tissues of all species. The δ15N ratios for the multispecies unionid community in the Huron River indicated some differences in nitrogen enrichment between species, the greatest enrichment being found in Pyganadon grandis. These δ15N ratios indicate that unionids may not always feed as primary consumers or omnivores. Stable-isotope data were critical for delineating diets and trophic-level interactions of this group of filter-feeders. Further refinements in identifying bacterial and picoplankton components of the fine particulate organic matter are needed to complete our understanding of resource partitioning between multispecies unionid populations.

REE investigation of the Motru Dyke System components from the Danubian basements (South Carpathians, Romania)

NASA Astrophysics Data System (ADS)

Campeanu, Mara; Balica, Constantin; Balintoni, Ioan; Tănăselia, Claudiu; Cadar, Oana

2017-04-01

Dragsan and Lainici-Paius groups represent the basement components of the Danubian Alpine units (South Carpathians, Romania), which consist of medium-grade metamorphic rocks. A subvolcanic system of dykes (i.e. Motru Dyke System - MDS) crosscut mostly the Lainici Paius basement as an effect of a late-Variscan termo-tectonic event. The geochemical features, frame the MDS components within a wide range of petrotypes (basaltic andesites to rhyolites), and define a wide differentiation series. Classically this subvolcanic system was inferred to be in connection to a unique mantle source [1], however, recent studies [2,3] suggest a mixed mantle-crust source, based on the interpretation of the trace elements in conjunction with Sr and Nd isotope data. Aditionally, the presence of relict zircon grains consolidates this assumption. New REE data collected from eight MDS components, generally confirm the mixed mantle-crust source hypothesis. The distribution patterns reveal two groups of samples. The first group (six samples) is moderately enriched in REE and shows moderately fractionated patterns with (La/Yb)N between 7-21 and low Eu/Eu* (0.81-0.9). The second group, strongly enriched in light REE, have high (La/Yb)N and strong negative Eu anomaly (Eu/Eu* of 0.41 and 0.38 respectively). REE vary between 107-147 ppm for the first group and 612 ppm - 907ppm for the second group. We can assume a stronger fractionation of plagioclase as well as of garnet and amphibole for the second group. With a flatter pattern, for the first group of samples, the fractionation of these minerals appears to be moderate. The emplacement age of MDS has been long disputed, since it was supposed as pre-Silurian for a long time. However, newly zircon U/Pb isotopic dating performed on two collected samples indicate a mean age of 300 My [2,3]. Owing to the croscutting relationships with the post-colisional granitoid plutons emplaced in the Danubian basement during the late Variscan, and based on new geochemical data, we consider that MDS was generated from a mixed mantle and crustal source, and emplaced in a post-collisional tectonic setting during the final stages of the Variscan orogeny. Acknowledgements: study supported by PN-II-ID-PCE-2011-3-0100 Grant, UEFIS-CDI and Core Program - ANCS PN 16.40.02.01. References: [1] Féménias, O., Berza, T., Tatu, M., Diot, H., Demaiffe, D., 2008. Nature and signifiance of a Cambro-Ordovician high-K, calc-alkaline sub-volcanic suite: the late- to post-orogenic Motru Dyke Swarm (Southern Carpathians, Romania), Int. J. Earth Sci. [2] Câmpeanu, M., Balica, C., Balintoni, I.C., 2014. Geochronology and emplacement conditions of Motru Dyke System (South Carpathians, Romania), Bul. Shk. Gjeol.2014- Special Issue, Vol 1/2014, Proceedings of XX CBGA Congress, Tirana, Albania, p.198. [3] Câmpeanu, M., Balica, C., Balintoni, I.C., Tanaselia, C., 2015. Motru Dyke Swarm (South Carpathians, Romania): Emplacement age and geotectonic setting (0) Goldschmidt Abstracts, 2015-459.

Elasticity of Orthoenstatite at High Pressure and Temperature: Implications for the Origin of Low VP/VS Zones in the Mantle Wedge

NASA Astrophysics Data System (ADS)

Qian, Wangsheng; Wang, Wenzhong; Zou, Fan; Wu, Zhongqing

2018-01-01

Orthopyroxene (opx) is an important mineral in petrologic models for the upper mantle. Its elastic properties are fundamental for understanding the chemical composition and geodynamics of the upper mantle. Here we calculate the elastic properties of orthoenstatite (MgSiO3), the Mg end-member orthopyroxene under upper mantle pressure and temperature conditions using first principle calculations with local density approximation. Bulk and shear moduli increase nonlinearly with pressure at mantle temperatures, but the shear modulus and VS show very weak pressure dependence in comparison with VP. Compared to other major minerals in the upper mantle, orthoenstatite has the lowest compressional velocities (VP), shear velocities (VS), and VP/VS ratio down to the depth of approximately 300 km. The enrichment of opx in the upper mantle can cause the unusually low VP/VS observed in the mantle wedge.

Petrochemistry of a xenolith-bearing Neogene alkali olivine basalt from northeastern Iran

NASA Astrophysics Data System (ADS)

Saadat, Saeed; Stern, Charles R.

2012-05-01

A small isolated Neogene, possibly Quaternary, monogenetic alkali olivine basalt cone in northeastern Iran contains both mantle peridotite and crustal gabbroic xenoliths, as well as plagioclase megacrysts. The basaltic magma rose to the surface along pathways associated with local extension at the junction between the N-S right-lateral and E-W left-lateral strike slip faults that form the northeastern boundary of the Lut microcontinental block. This basalt is enriched in LREE relative to HREE, and has trace-element ratios similar to that of oceanic island basalts (OIB). Its 87Sr/86Sr (0.705013 to 0.705252), 143Nd/144Nd (0.512735 to 0.512738), and Pb isotopic compositions all fall in the field of OIB derived from enriched (EM-2) mantle. It formed by mixing of small melt fractions from both garnet-bearing asthenospheric and spinel-facies lithospheric mantle. Plagioclase (An26-32) megacrysts, up to 4 cm in length, have euhedral crystal faces and show no evidence of reaction with the host basalt. Their trace-element concentrations suggest that these megacrysts are co-genetic with the basalt host, although their 87Sr/86Sr (0.704796) and 143Nd/144Nd (0.512687) ratios are different than this basalt. Round to angular, medium-grained granoblastic meta-igneous gabbroic xenoliths, ranging from ~ 1 to 6 cm in dimension, are derived from the lower continental crust. Spinel-peridotite xenoliths equilibrated in the subcontinental lithosphere at depths of 30 to 60 km and temperatures of 965 °C to 1065 °C. These xenoliths do not preserve evidence of extensive metasomatic enrichment as has been inferred for the mantle below the Damavand volcano further to the west in north-central Iran, and clinopyroxenes separated from two different mantle xenoliths have 87Sr/86Sr (0.704309 and 0.704593) and 143Nd/144Nd (0.512798) ratios which are less radiogenic than either their host alkali basalt or Damavand basalts, implying significant regional variations in the composition and extent of metasomatism in the sub-Iranian mantle.

Mid-Neoproterozoic intraplate magmatism in the northern margin of the Southern Granulite Terrane, India: Constraints from geochemistry, zircon U-Pb geochronology and Lu-Hf isotopes

NASA Astrophysics Data System (ADS)

Deeju, T. R.; Santosh, M.; Yang, Qiong-Yan; Pradeepkumar, A. P.; Shaji, E.

2016-11-01

The northern margin of the Southern Granulite Terrane in India hosts a number of mafic, felsic and alkaline magmatic suites proximal to major shear/paleo-suture zones and mostly represents magmatism in rift-settings. Here we investigate a suite of gabbros and granite together with intermediate (dioritic) units generated through mixing and mingling of a bimodal magmatic suite. The massive gabbro exposures represent the cumulate fraction of a basic magma whereas the granitoids represent the product of crystallization in felsic magma chambers generated through crustal melting. Diorites and dioritic gabbros mostly occur as enclaves and lenses within host granitoids resembling mafic magmatic enclaves. Geochemistry of the felsic units shows volcanic arc granite and syn-collisional granite affinity. The gabbro samples show mixed E-MORB signature and the magma might have been generated in a rift setting. The trace and REE features of the rocks show variable features of subduction zone enrichment, crustal contamination and within plate enrichment, typical of intraplate magmatism involving the melting of source components derived from both depleted mantle sources and crustal components derived from older subduction events. The zircons in all the rock types show magmatic crystallization features and high Th/U values. Their U-Pb data are concordant with no major Pb loss. The gabbroic suite yields 206Pb/238U weighted mean ages in the range of 715 ± 4-832.5 ± 5 Ma marking a major phase of mid Neoproterozoic magmatism. The diorites crystallized during 206Pb/238U weighted mean age of 724 ± 6-830 ± 2 Ma. Zircons in the granite yield 206Pb/238U weighted mean age of 823 ± 4 Ma. The age data show broadly similar age ranges for the mafic, intermediate and felsic rocks and indicate a major phase of bi-modal magmatism during mid Neoproterozoic. The zircons studied show both positive and negative εHf(t) values for the gabbros (-6.4 to 12.4), and negative values for the diorites (-7.8 to -16.7) and granite (-16.6 to -6.7). Together with the Hf depleted model ages and crustal model ages, we infer that the magma sources involved both juvenile depleted mantle and reworked Mesoproterozoic, Paleoproterozoic and Neoarchean components. The mid Neoproterozoic intraplate magmatism is considered to be a response to mantle upwelling in an aborted rift setting.

Origin of heavy REE mineralisation in carbonatites: Constraints form the Huanglongpu Mo-HREE deposit, Qinling, China.

NASA Astrophysics Data System (ADS)

Smith, Martin; Cheng, Xu; Kynicky, Jindrich; Cangelosi, Delia; Wenlei, Song

2017-04-01

The carbonatite dykes of the Huanglongpu area, Lesser Qinling, China, are unusual in that they are quartz-bearing, Mo-mineralised and enriched in the heavy rare earth elements (HREE) relative to typical carbonatites. Carbonatite monazite (208.9±4.6 Ma to 213.6±4.0; Song et al., 2016) gives a comparable U-Pb radiometric age to molybdenite (220Ma; Stein et al., 1997), confirming interpretations that Mo is derived from the carbonatite, and not a subsequent overprint from regional porphyry-style mineralisation ( 141Ma). The sulphides in the carbonatites have mantle-like 34S ( 1‰) and low δ26Mg values (-1.89 to -1.07‰), similar to sedimentary carbonates, suggesting a recycled sediment contribution in their mantle sources that may be responsible for the Mo and HREE enrichment (Song et al., 2016). The textures of REE minerals indicate crystallisation of monazite-(Ce), bastnäsite-(Ce), parisite-(Ce) and aeschynite-(Ce) as magmatic phases. Monazite-(Ce) was subsequently altered to produce apatite, which was in turn replaced by britholite-(Ce), accompanied by the formation of allanite-(Ce). The REE-fluorcarbonates where replaced by synchysite-(Ce) and röntgenite-(Ce). Aeschynite-(Ce) was altered initially to uranopyrochlore and then pyrochlore with uraninite inclusions. The mineralogical evolution reflects the evolution from magmatic carbonatite, through to more silica-rich conditions during the magmatic-hydrothermal transition, to fully hydrothermal conditions accompanied by the formation of sulphate minerals. Each alteration stage resulted in the preferential leaching of the LREE and enrichment in the HREE. Mass balance considerations indicate that the HREE enrichment could not be a passive process, and that hydrothermal fluids must have contributed HREE to the system. The evolution of the fluorcarbonate mineral assemblage requires an increase in aCa2+ and aCO32- in the metasomatic fluid, and so breakdown of HREE-enriched calcite may have been the HREE source. Solubility products are lower for LREE minerals compared to HREE minerals, so leaching in the presence of strong, LREE-selective ligands (Cl-, CO32-) may account for the depletion in late stage minerals in the LREE, but cannot account for subsequent preferential HREE addition. Fluid inclusion data indicate the presence of sulphate-rich brines during late stage alteration, and hence sulphate complexation may have been important for preferential HREE transport, as sulphate has been shown to be non-LREE selective during the formation of complex ions. The combination of mantle source with a recycled oceanic sediment component, and REE enrichment during magmatic processes, and late stage alteration with non-LREE selective ligands such as sulphate may be critical in forming HREE-enriched carbonatites. Song et al., (2016) Origin of unusual HREE-Mo-rich carbonatites in the Qinling orogen, China. Scientific Reports, 6:37377 | DOI: 10.1038/srep37377. Stein et al. (1997) Highly precise and accurate Re-Os ages for molybdenite from the East Qinling-Dabie molybdenum belt, Shaanxi province, China. Econ. Geol. 92, 827-835 (1997)

How inheritance, geochemical and geophysical properties of the lithospheric mantle influence rift development and subsequent collision

NASA Astrophysics Data System (ADS)

Picazo, Suzanne; Chenin, Pauline; Müntener, Othmar; Manatschal, Gianreto; Karner, Garry; Johnson, Christopher

2017-04-01

In magma-poor rifted margins, the rift structures, width of necking zones and overall geometry are controlled by the heterogeneities of geochemical and geophysical properties of the crust and mantle. In this presentation we focus on the mantle heterogeneities and their major implications on the closure of a hyper-extended rifted system. In our study, we review the clinopyroxene and spinel major element composition from the Liguria-Piemonte domain, the Pyrenean domain, the Dinarides and Hellenides ophiolites and the Iberia-Newfoundland rifted margins (Picazo et al, 2016). It would seem that during an extensional cycle i.e., from post-orogenic collapse to polyphase rifting to seafloor spreading, the mineral compositions of mantle peridotites are systematically modified. The initially heterogeneous subcontinental mantle cpx (inherited mantle type 1) equilibrated in the spinel peridotite field and is too enriched in Na2O and Al2O3 to be a residue of syn-rift melting. The heterogeneous inherited subcontinental mantle becomes progressively homogenized due to impregnation by MORB-type melts (refertilized mantle-type 2) during extensional thinning of the lithosphere. At this stage, cpx equilibrate with plagioclase and display lower Na2O and Al2O3 and high Cr2O3 contents. The system might evolve into breakup and oceanization (mantle type 3) i.e., self-sustained steady-state seafloor spreading. The different mantle-types are present in various reconstructed sections of magma-poor margins and display a systematic spatial distribution from mantle type 1 to 3 going oceanwards in Western and Central Europe. We estimated the density of the three identified mantle types using idealized modal peridotite compositions using the algorithm by Hacker et al, (2003). The density of the refertilized plagioclase peridotite is predicted to be lower than that of inherited subcontinental and depleted oceanic mantle. This has some interesting consequences on the reactivation of rifted margins. Conversely to a classical subduction where the oceanic lithosphere being subducted produces a mobile component that contributes to the formation of long-lived volcanic arcs, a hyper-extended rifted system and small oceanic basins (<300m wide) might not go to self-sustained subduction with limited production of arc magmas. Such a mantle wedge might remains fertile with a high potential to melt during the first stages of subsequent extension. Hacker, B. R., Abers, G. A., and Peacock, S. M. (2003). Subduction factory 1. Theoretical mineralogy, densities, seismic wave speeds, and H2O contents. Journal of Geophysical Research, 108(B1):2029. Picazo, S., Müntener, O., Manatschal, G., Bauville, A., Karner, G., & Johnson, C. (2016). Mapping the nature of mantle domains in Western and Central Europe based on clinopyroxene and spinel chemistry: Evidence for mantle modification during an extensional cycle. Lithos, 266, 233-263.

Possible solar noble-gas component in Hawaiian basalts

USGS Publications Warehouse

Honda, M.; McDougall, I.; Patterson, D.B.; Doulgeris, A.; Clague, D.A.

1991-01-01

THE noble-gas elemental and isotopic composition in the Earth is significantly different from that of the present atmosphere, and provides an important clue to the origin and history of the Earth and its atmosphere. Possible candidates for the noble-gas composition of the primordial Earth include a solar-like component, a planetary-like component (as observed in primitive meteorites) and a component similar in composition to the present atmosphere. In an attempt to identify the contributions of such components, we have measured isotope ratios of helium and neon in fresh basaltic glasses dredged from Loihi seamount and the East Rift Zone of Kilauea1-3. We find a systematic enrichment in 20Ne and 21Ne relative to 22Ne, compared with atmospheric neon. The helium and neon isotope signatures observed in our samples can be explained by mixing of solar, present atmospheric, radiogenic and nucleogenic components. These data suggest that the noble-gas isotopic composition of the mantle source of the Hawaiian plume is different from that of the present atmosphere, and that it includes a significant solar-like component. We infer that this component was acquired during the formation of the Earth.

The peculiar case of Marosticano xenoliths: a cratonic mantle fragment affected by carbonatite metasomatism in the Veneto Volcanic Province (Northern Italy)

NASA Astrophysics Data System (ADS)

Brombin, Valentina; Bonadiman, Costanza; Coltorti, Massimo; Florencia Fahnestock, M.; Bryce, Julia G.; Marzoli, Andrea

2017-04-01

The Tertiary Magmatic Province of Veneto, known as Veneto Volcanic Province (VVP), in the Northern Italy, represents one of the most important volcanic provinces of the Adria Plate. It is composed by five volcanic districts: Val d'Adige, Marosticano, Mts. Lessini, Berici Hills and Euganean Hills. Most of the volcanic products are relatively undifferentiated lavas, from nephelinites to tholeiites in composition. Commonly VVP nephelinites and basanites carry mantle xenoliths. This study presents a petrological characterization of the new xenolith occurrence of Marosticano and comparison with previously studied VVP xenolith populations (i.e. from the Lessinean and Val d'Adige areas), which represent off-craton lithospheric mantle fragment affected by Na-alkaline silicate metasomatism (Siena & Coltorti 1989; Beccaluva et al., 2001; Gasperini et al., 2006). Marosticano (MA) peridotites are anhydrous spinel-bearing lherzolites and harzburgites, which are geochemically well distinguishible from the other VVP mantle xenoliths. Primary minerals record the "most restitic" composition of the VVP sampled mantle, even calling the geochemical features of a sub-cratonic mantle. Olivines in both lherzolites and harzburgites show high Ni contents compared with the Fo values (Ni→ lherzolite: 2600-3620 ppm; harzburgite: 2600-3540 ppm; Fo → lh: 91-92; hz: 90-93) that follow the trend of olivine from a cratonic area (Kelemen, 1998). Orthopyroxenes have mg# values with 1:1 ratio with coexisting olivines and Al2O3 contents always <4 wt%, even for the most fertile lherzolite. Low Al2O3 (<5 wt%) associated with high Cr2O3 (>0.5 wt%) contents are also the chemical characteristics of the clinopyroxenes. On the whole both MA pyroxenes show major element contents that recall the characteristics of those from cratonic (sp-bearing) peridotites (e.g. from Greenland, South Africa and Tanzania; Downes et al., 2004). In addition, the relationship between the high Fo content of olivine and the high chromium contents (cr#=(Cr/(Cr+Al)X100); lh: 30-53; hz: 38-67) in coexisting spinel, out of the typical OSMA array (Arai, 1994b) is observed in typical on-craton mantle rocks (Downes et al., 2004). To corroborate the cratonic "flavour" of these peridotites, in-situ trace element analyses show that Marosticano clinopyroxene have modified their residual characteristics by interaction with deep metasomatic melt, which was able to strong enrich in U, Th, LILE (Rb-Ba) and LREE with respect to the restitic preserved HREE and HFSE (e.g. Nb, Ta, Zr and Hf) contents. The general clinopyroxene trace element distribution and elemental ratios ((La/Yb)N and Ti/Eu; Coltorti et al., 1999) are consistent with enrichment provided by a carbonatitic rather than a silicate metasomatizing agent. To characterize the chemical-physical frame of the MA mantle segment, peridotites equilibration temperatures and oxygen fugacities were also estimated and compared with those of the other VVP xenoliths. The latter comparison leads to i) Marosticano samples record relatively high oxidation conditions (as Mts. Lessini peridotites) in agreement with the range assigned to continental lithosphere (Foley et al., 2011) and ii) these T-fO2 values account for CO2 mole fractions dissolved in a potential metasomatic melt close to 1, further supporting the carbonatitic nature of the infiltrating melt. In this case it can be speculated that the usually low oxidizing conditions of the cratonic mantle have been augmented by the interaction with a carbonatitic melt or with a CO2-rich fluid released by the reaction with a peridotitic matrix. References Arai, S., 1994b. Compositional variation of olivine chromian spinel in Mg-rich magmas as a guide to their residual spinel peridotites. Journal of Volcanology and Geothermal Research 59, 279-293. Beccaluva L., Bianchini G., Bonadiman C., Coltorti M., Milani L., Salvini L., Siena F., Tassinari R. (2007). Intraplate lithospheric and sublithospheric components in the Adriatic domain: Nephelinite to tholeiite magma generation in the Paleogene Veneto Volcanic Province, Southern Alps. Geological Society of America, 131-152. Beccaluva L., Bonadiman C., Coltorti M., Salvini L., Siena F. (2001). Depletion events, nature of metasomatizing agent and timing of enrichment processes in lithospheric mantle xenoliths from the Veneto Volcanic Province. Journal of Petrology, 42, 173-187. Coltorti, M., Bonadiman, C., Hinton, R.W., Siena, F., Upton, B.G.J. (1999). Carbonatite metasomatism of the oceanic upper mantle: evidence from clinopyroxenes and glasses in ultramafic xenoliths of Grande Comore, Indian Ocean. Journal of Petrology, 40, 133-165. Downes, H., MacDonald, R., Upton, B.G.J., Cox, K.G, Bodinier, J-L, Mason, P.R.D, James, D., Hill, P.G., Hearn, C. Jr (2004). Ultramafic xenoliths from the Bearpaw Mountains, Montana, USA: evidence for multiple metasomatic events in the lithospheric mantle beneath the Wyoming Carton. Journal of Petrology, 45, 1631-1662. Foley, S.F. (2011). A reappraisal of redox melting in the Earth's mantle as a function of tectonic setting and time. Journal of Petrology, 52, 1363-1391. Gasperini D., Bosch D., Braga R., Bondi M., Macera P., Morten L. (2006). Ultramafic xenoliths from the Veneto Volcanic Province (Italy): Petrological and geochemical evidence for multiple metasomatism of the SE Alps mantle lithospere. Geochemical Journal, 40, 377-404. Kelemen, P.B., Hart, S.R., Bernstein, S. (1998). Silica enrichment in the continental upper mantle via melt/rock reaction. Earth and Planetary Science Letters, 164, 387-406. Ramsey, R.R, Tompkins, L.A. (1994). The geology, heavy mineral concentrate mineralogy, and diamond prospectivity of the Boa Esperança and Cana Verde pipes, Corrego D'anta, Minas Gerais, Brazil, in: Meyer, H.O.A and Leonardos, O.H. (Eds.), Proceeding of the Fifth International Kimberlite Conference 2. Companhia de Pesquisa de Recursors Minerais, Special Publications, 329-345. Siena F., Coltorti M. (1989). Lithospheric mantle evolution: evidences from ultramafic xenoliths in the Lessinean volcanics (Northern Itlay). Chemical Geology, 77, 347-364.

The Lowest δ7Li Yet Recorded in MORB Glasses: The Connection with Oceanic Core Complex Formation, Refractory Rutile-bearing Eclogitic Mantle Sources and Melt Supply

NASA Astrophysics Data System (ADS)

Casey, J. F.; Gao, Y.; Benavidez, R.; Dragoi, C.

2010-12-01

The region between 12°N and 16°N along the Mid-Atlantic Ridge is known for its prolific development of oceanic core complexes and for a geochemical anomaly centered at ~14°N. We examine the correlation of the geochemical anomaly with a region characterized by low magma supply. Basalt glasses over the geochemical anomaly are unusual in exhibiting E-MORB to T-MORB HIMU-DMM isotopic gradients. The most enriched MORBs exhibit positive Ta and Nb anomalies and negative Th and Pb anomalies that are similar to some OIB basalts. Some more primitive basalts exhibit positive Ti, Sr and Eu anomalies. The center of the geochemical anomaly is characterized by elevated La/Sm ratios that are strongly correlated with Nb/La, Nb/Nb*, Ta/Ta* and Sr, Nd, Pb isotopic anomalies. In addition, we have recently documented a regional anomaly in δ7Li, with the lowest values ever recorded in MORB glasses near the center of the anomaly. We interpret this data to indicate that the mantle source in the 12-16°N region of the Mid-Atlantic Ridge involves subducted slab components including a refractory rutile-bearing eclogitic source that has suffered significant dehydration and a previously depleted mantle source that has undergone an ancient depletion event that results in little melt supply being contributed to the ridge axis. We examine melt supply implications in the context of core complex development and these unusual mantle source characteristics.

The paradox of a wet (high H2O) and dry (low H2O/Ce) mantle: High water concentrations in mantle garnet pyroxenites from Hawaii

NASA Astrophysics Data System (ADS)

Bizimis, M.; Peslier, A. H.

2013-12-01

Water dissolved as trace amounts in anhydrous minerals has a large influence on the melting behavior and physical properties of the mantle. The water concentration of the oceanic mantle is inferred from the analyses of MORB and OIB [1], but there is little data from actual mantle samples. Moreover, enriched mineralogies (pyroxenites, eclogites) are thought as important sources of heterogeneity in the mantle, but their water concentrations and their effect on the water budget and cycling in the mantle are virtually unknown. We analyzed by FTIR water concentrations in garnet clinopyroxenite xenoliths from Salt Lake Crater, Oahu, Hawaii. These pyroxenites are high-pressure (>20kb) crystal fractionates from alkalic melts. The clinopyroxenes (cpx) have 260 to 576 ppm wt. H2O, with the least differentiated samples (Mg#>0.8) in the 400-500 ppm range. Orthopyroxene (opx) contain 117-265 ppm H2O, about half of that of cpx, consistent with other natural sample studies, but lower than experimental cpx/opx equilibrium data. These pyroxenite cpx and opx water concentrations are at the high-end of on-and off-craton peridotite xenolith concentrations and megacrysts from kimberites [2] and those of Hawaiian spinel peridotites. In contrast, garnet has extremely low water contents (<5ppm H2O). There is no correlation between water in cpx and lithophile element concentrations. Phlogopite is present in some samples, and its modal abundance shows a positive correlation in Mg# with cpx, implying equilibrium. However, there is no correlation between water concentrations and the presence of phlogopite. These data imply that cpx and opx water concentrations may be buffered by phlogopite crystallization. Reconstructed bulk rock pyroxenite water concentrations (not including phlogopite, i.e. minimum) range from 200-460 ppm (average 331× 75 ppm), significantly higher than water estimates for the MORB source (50-200 ppm), but in the range of E-MORB, OIB and the source of rejuvenated Hawaiian magmas [1,3]. The average bulk rock pyroxenite H2O/Ce is 69 × 35, lower than estimates of the MORB source (~150) or FOZO, C (200-250) mantle component, but consistent with 'dry' EM sources (<100) [1]. These data suggest that a metasomatized, refertilized oceanic lithosphere that contains a pyroxenite component (e.g. in the lower part of an oceanic plate, where ascending melts can become trapped and crystallize), will have both higher water concentrations and low H2O/Ce, and may contribute to EM-type OIB sources, like that of Samoan basalts [5]. Therefore, a low H2O/Ce mantle source may not necessarily be 'dry'. [1] Dixon et al., 2002, Nature 420, 385-389. [2] Peslier, 2010 JVGR 197, 239-258. [3] Dixon et al., 1997 JP 38, 911-939. [4] O'Leary et al. 2010 EPSL 297, 111-120. [5] Workman et al., 2006 EPSL 241, 932 - 951.

The role of solid-solid phase transitions in mantle convection

NASA Astrophysics Data System (ADS)

Faccenda, Manuele; Dal Zilio, Luca

2017-01-01

With changing pressure and temperature conditions, downwelling and upwelling crustal and mantle rocks experience several solid-solid phase transitions that affect the mineral physical properties owing to structural changes in the crystal lattice and to the absorption or release of latent heat. Variations in density, together with phase boundary deflections related to the non-null reaction slope, generate important buoyancy forces that add to those induced by thermal perturbations. These buoyancy forces are proportional to the density contrast between reactant and product phases, their volume fraction, the slope and the sharpness of the reaction, and affect the style of mantle convection depending on the system composition. In a homogeneous pyrolitic mantle there is little tendency for layered convection, with slabs that may stagnate in the transition zone because of the positive buoyancy caused by post-spinel and post-ilmenite reactions, and hot plumes that are accelerated by phase transformations in the 600-800 km depth range. By adding chemical and mineralogical heterogeneities as on Earth, phase transitions introduce bulk rock and volatiles filtering effects that generate a compositional gradient throughout the entire mantle, with levels that are enriched or depleted in one or more of these components. Phase transitions often lead to mechanical softening or hardening that can be related to a different intrinsic mechanical behaviour and volatile solubility of the product phases, the heating or cooling associated with latent heat, and the transient grain size reduction in downwelling cold material. Strong variations in viscosity would enhance layered mantle convection, causing slab stagnation and plume ponding. At low temperatures and relatively dry conditions, reactions are delayed due to the sluggish kinetics, so that non-equilibrium phase aggregates can persist metastably beyond the equilibrium phase boundary. Survival of low-density metastable olivine, Ringwoodite, pyroxene and pyrope garnet in the transition zone and uppermost lower mantle produces positive buoyancy forces that decrease the subduction velocity and may lead to slab stagnation in the transition zone. The presence of deep metastable portions is still debated, and should not be associated a-priori with a completely dry slab as field observations suggest that heterogeneously hydrated oceanic plates could contain metastable dry portions surrounded by transformed wet rocks.

Subducted slab-plume interaction traced by magnesium isotopes in the northern margin of the Tarim Large Igneous Province

NASA Astrophysics Data System (ADS)

Cheng, Zhiguo; Zhang, Zhaochong; Xie, Qiuhong; Hou, Tong; Ke, Shan

2018-05-01

Incorporation of subducted slabs may account for the geochemical and isotopic variations of large igneous provinces (LIPs). However, the mechanism and process by which subducted slabs are involved into magmas is still highly debated. Here, we report a set of high resolution Mg isotopes for a suite of alkaline and Fe-rich rocks (including basalts, mafic-ultramafic layered intrusions, diabase dykes and mantle xenoliths in the kimberlitic rocks) from Tarim Large Igneous Province (TLIP). We observed that δ26 Mg values of basalts range from -0.29 to - 0.45 ‰, -0.31 to - 0.42 ‰ for mafic-ultramafic layered intrusions, -0.28 to - 0.31 ‰ for diabase dykes and -0.29 to - 0.44 ‰ for pyroxenite xenoliths from the kimberlitic rocks, typically lighter than the normal mantle source (- 0.25 ‰ ± 0.04, 2 SD). After carefully precluding other possibilities, we propose that the light Mg isotopic compositions and high FeO contents should be ascribed to the involvement of recycled sedimentary carbonate rocks and pyroxenite/eclogite. Moreover, from basalts, through layered intrusions to diabase dykes, (87Sr/86Sr)i values and δ18OV-SMOW declined, whereas ε (Nd) t and δ26 Mg values increased with progressive partial melting of mantle, indicating that components of carbonate rock and pyroxenite/eclogite in the mantle sources were waning over time. In combination with the previous reported Mg isotopes for carbonatite, nephelinite and kimberlitic rocks in TLIP, two distinct mantle domains are recognized for this province: 1) a lithospheric mantle source for basalts and mafic-ultramafic layered intrusions which were modified by calcite/dolomite and eclogite-derived high-Si melts, as evidenced by enriched Sr-Nd-O and light Mg isotopic compositions; 2) a plume source for carbonatite, nephelinite and kimberlitic rocks which were related to magnesite or periclase/perovskite involvement as reflected by depleted Sr-Nd-O and extremely light Mg isotopes. Ultimately, our study suggests that subducted slabs could make important contributions to LIP generation, and establishes a potential linkage between plate tectonics and mantle plume.

Fluid-mediated mass transfer from a paleosubduction channel to its mantle wedge: Evidence from jadeitite and related rocks from the Guatemala Suture Zone

NASA Astrophysics Data System (ADS)

Harlow, George E.; Flores, Kennet E.; Marschall, Horst R.

2016-08-01

Jadeitites in serpentinite mélanges are the product of crystallization from and/or metasomatism by aqueous fluids that transfer components from and within a subduction channel-the slab-mantle interaction volume-into discrete rock units, most commonly found within the serpentinized or serpentinizing portion of the channel or the overlying mantle rocks at high pressure (1 to > 2 GPa). Two serpentinite mélanges on either side of the Motagua fault system (MFS) of the Guatemala Suture Zone contain evidence of this process. Whole rock compositional analyses are reported here from 86 samples including jadeitites and the related rocks: omphacitites, albitites and mica rocks. The predominance of a single phase in most of these rocks is reflected in the major element compositions and aspects of the trace elements, such as REE abundances tracking Ca in clinopyroxene. Relative to N-MORB all samples show relative enrichments in the high field strength elements (HFSE) Hf, Zr, U, Th, and the LILE Ba and Cs, contrasted by depletions in K and in some cases Pb or Sr. Most jadeitites are also depleted in the highly compatible elements Cr, Sc and Ni despite their occurrence in serpentinite mélange; however, some omphacitite samples show the opposite. Trace elements in these jadeitite samples show a strong similarity with GLOSS (globally subducted oceanic sediment) and other terrigenous sediments in terms of their trace-element patterns, but are offset to lower abundances. Jadeitites thus incorporate a strong trace-element signature derived from sediments mixed with that from fluid derived from altered oceanic crust. Enrichment in the HFSE argues for mobility of these elements in aqueous fluids at high P/T conditions in the subduction channel and a remarkable lack of fractionation that might otherwise be expected from dissolution and fluid transport.

Molybdenum isotope fractionation in the mantle

NASA Astrophysics Data System (ADS)

Liang, Yu-Hsuan; Halliday, Alex N.; Siebert, Chris; Fitton, J. Godfrey; Burton, Kevin W.; Wang, Kuo-Lung; Harvey, Jason

2017-02-01

We report double-spike molybdenum (Mo) isotope data for forty-two mafic and fifteen ultramafic rocks from diverse locations and compare these with results for five chondrites. The δ98/95Mo values (normalized to NIST SRM 3134) range from -0.59 ± 0.04 to +0.10 ± 0.08‰. The compositions of one carbonaceous (CI) and four ordinary chondrites are relatively uniform (-0.14 ± 0.01‰, 95% ci (confidence interval)) in excellent agreement with previous data. These values are just resolvable from the mean of 10 mid-ocean ridge basalts (MORBs) (0.00 ± 0.02‰, 95% ci). The compositions of 13 mantle-derived ultramafic xenoliths from Kilbourne Hole, Tariat and Vitim are more diverse (-0.39 to -0.07‰) with a mean of -0.22 ± 0.06‰ (95% ci). On this basis, the isotopic composition of the bulk silicate Earth (BSE or Primitive Mantle) is within error identical to chondrites. The mean Mo concentration of the ultramafic xenoliths (0.19 ± 0.07 ppm, 95% ci) is similar in magnitude to that of MORB (0.48 ± 0.13 ppm, 95% ci), providing evidence, either for a more compatible behaviour than previously thought or for selective Mo enrichment of the subcontinental lithospheric mantle. Intraplate and ocean island basalts (OIBs) display significant isotopic variability within a single locality from MORB-like to strongly negative (-0.59 ± 0.04‰). The most extreme values measured are for nephelinites from the Cameroon Line and Trinidade, which also have anomalously high Ce/Pb and low Mo/Ce relative to normal oceanic basalts. δ98/95Mo correlates negatively with Ce/Pb and U/Pb, and positively with Mo/Ce, explicable if a phase such as an oxide or a sulphide liquid selectively retains isotopically heavy Mo in the mantle and fractionates its isotopic composition in low degree partial melts. If residual phases retain Mo during partial melting, it is possible that the [Mo] for the BSE may be misrepresented by values estimated from basalts. This would be consistent with the high Mo concentrations of all the ultramafic xenoliths of 40-400 ppb, similar to or, significantly higher than, current estimates for the BSE (39 ppb). On this basis a revised best estimate of the Mo content in the BSE based on these concentrations would be in the range 113-180 ppb, significantly higher than previously assumed. These values are similar to the levels of depletion in the other refractory moderately siderophile elements W, Ni and Co. A simpler explanation may be that the subcontinental lithospheric mantle has been selectively enriched in Mo leading to the higher concentrations observed. Cryptic melt metasomatism would be difficult to reconcile with the high Mo/Ce of the most LREE depleted xenoliths. Ancient Mo-enriched subducted components would be expected to have heavy δ98/95Mo, which is not observed. The Mo isotope composition of the BSE, cannot be reliably resolved from that of chondrites at this time despite experimental evidence for metal-silicate fractionation. An identical isotopic composition might result from core-mantle differentiation under very high temperatures such as were associated with the Moon-forming Giant Impact, or from the BSE inventory reflecting addition of moderately siderophile elements from an oxidised Moon-forming impactor (O'Neill, 1991). However, the latter would be inconsistent with the non-chondritic radiogenic W isotopic composition of the BSE. Based on mantle fertility arguments, Mo in the BSE could even be lighter (lower 98/95Mo) than that in chondrites, which might be explained by loss of S rich liquids from the BSE during core formation (Wade et al., 2012). Such a late removal model is no longer required to explain the Mo concentration of the BSE if its abundance is in fact much higher, and similar to the values for ultramafic xenoliths.

New constraints on the geochronology and Sm-Nd isotopic characteristics of Bas-Drâa mafic dykes, Anti-Atlas of Morocco

NASA Astrophysics Data System (ADS)

El Bahat, Abdelhakim; Ikenne, Moha; Cousens, Brian; Söderlund, Ulf; Ernst, Richard; Klausen, Martin B.; Youbi, Nasrrddine

2017-03-01

The Precambrian inliers of the Anti-Atlas belt across the southern part of Morocco contain numerous mafic dyke and sill swarms, which are thought to represent the erosional remnants of Proterozoic Large Igneous Provinces (LIPs). As part of an extended research campaign to date and characterize these LIPs, two amphiboles from one dyke within the Bas-Drâa inlier (western Anti-Atlas) yielded consistent 40Ar-39Ar ages of 611 Ma ± 1.3; i.e., evidence of magmatic activity during the Ediacaran (635-542 Ma). Furthermore, Nd isotope ratios and model ages identifies four groups of dykes within the Bas-Drâa inlier, all of which were derived from a previously enriched mantle reservoir with very low 143Nd/144Nd ratios (0.51065-0.51170) and corresponding εNd(t) values (-16.44 to -2.45). Such low Nd-ratios arguably reflect either a contribution of crustal components, such as the Paleoproterozoïc schisto-granitic basement, or metasomatic modification of the sub-continental lithospheric mantle.

Metasomatic Enrichment of Oceanic Lithospheric Mantle Documented by Petit-Spot Xenoliths

NASA Astrophysics Data System (ADS)

Pilet, S.; Abe, N.; Rochat, L.; Hirano, N.; Machida, S.; Kaczmarek, M. A.; Muntener, O.

2015-12-01

Oceanic lithosphere is generally interpreted as mantle residue after MORB extraction. It has been proposed, however, that metasomatism could take place at the interface between the low-velocity zone and the cooling and thickening oceanic lithosphere or by the percolation of low-degree melts produced in periphery of Mid Ocean Ridges. This later process is observed in slow spreading ridges and ophiolites where shallow oceanic lithospheric mantle could be metasomatized/refertilized during incomplete MORB melt extraction. Nevertheless, direct evidence for metasomatic refertilization of the deep part of the oceanic lithospheric mantle is still missing. Xenoliths and xenocrysts sampled by petit-spot volcanoes interpreted as low-degree melts extracted from the base of the lithosphere in response to plate flexure, provide important new information about the nature and the processes associated with the evolution of oceanic lithospheric mantle. Here, we report, first, the presence of a garnet xenocryst in petit-spot lavas from Japan characterized by low-Cr, low-Ti content and mostly flat MREE-HREE pattern. This garnet is interpreted as formed during subsolidus cooling of pyroxenitic or gabbroic cumulates formed at ~1 GPa during the incomplete melt extraction at the periphery of the Pacific mid-ocean ridge. It is the first time that such processes are documented in fast spreading context. Second, we report petit-spot mantle xenoliths with cpx trace element "signatures" characterized by high U, Th, relative depletion in Nb, Pb, Ti and high but variable LREE/HREE ratio suggesting equilibration depth closed to the Gt/Sp transition zone. Such "signatures" are unknown from oceanic settings and show unexpected similarity to melt-metasomatized gt-peridotites sampled by kimberlites. This similarity suggests that metasomatic processes are not restricted to continental setting, but could correspond to a global mechanism at the lithosphere-asthenosphere boundary. As plate flexure represents a global mechanism in subduction zone, a portion of oceanic lithospheric mantle is likely to be metasomatized; recycling of these enriched domains into the convecting mantle is fundamental to understand the generation of small scale mantle isotopic and volatile heterogeneities sampled by OIBs and MORBs.

Constraints from Earth's heat budget on mantle dynamics

NASA Astrophysics Data System (ADS)

Kellogg, L. H.; Ferrachat, S.

2006-12-01

Recent years have seen an increase in the number of proposed models to explain Earth's mantle dynamics: while two end-members, pure layered convection with the upper and lower mantle convecting separately from each other, and pure, whole mantle convection, appear not to satisfy all the observations, several addition models have been proposed. These models include and attempt to characterize least one reservoir that is enriched in radiogenic elements relative to the mid-ocean ridge basalt (MORB) source, as is required to account for most current estimates of the Earth's heat budget. This reservoir would also be responsible for the geochemical signature in some ocean island basalts (OIBs) like Hawaii, but must be rarely sampled at the surface. Our current knowledge of the mass- and heat-budget for the bulk silicate Earth from geochemical, cosmochemical and geodynamical observations and constraints enables us to quantify the radiogenic heat enrichment required to balance the heat budget. Without assuming any particular model for the structure of the reservoir, we first determine the inherent trade-off between heat production rate and mass of the reservoir. Using these constraints, we then investigate the dynamical inferences of the heat budget, assuming that the additional heat is produced within a deep layer above the core-mantle boundary. We carry out dynamical models of layered convection using four different fixed reservoir volumes, corresponding to deep layers of thicknesses 150, 500 1000 and 1600 km, respectively, and including both temperature-dependent viscosity and an instrinsic viscosity jump between upper and lower mantle. We then assess the viability of these cases against 5 criteria: stability of the deep layer through time, topography of the interface, effective density profile, intrinsic chemical density and the heat flux at the CMB.

Neogene volcanism associated with back-arc basin tectonics at the northern Fossa Magna, NE Japan

NASA Astrophysics Data System (ADS)

Okamura, S.; Inaba, M.; Shinjo, R.; Adachi, Y.

2016-12-01

New isotopic and trace element data presented here imply a temporal change in magma sources and thermal conditions beneath the northern Fossa Magna of NE Japan from the Miocene to the Pliocene. Rocks from more sediment melt-rich Early Miocene volcanoes have less radiogenic 176Hf/177Hf and 143Nd/144Nd, high Zr/Hf, and little or no Hf anomaly (Hf/Hf*; ˜1.0). The mantle wedge in the Early Miocene consisted of enriched mantle source. We propose that during the onset of subduction, influx of hot asthenospheric mantle provided sufficient heat to partially melt newly subducting sediment. Geochemical modeling results suggest breakdown of zircon in the slab surface sediments for the Early Miocene lavas in the northern Fossa Magna region. In the Middle Miocene, the injection of hot and depleted asthenospheric material replaced the mantle beneath the northern Fossa Magna region of NE Japan. This caused the isotopic signature of the rocks to change from enriched to depleted. The Middle Miocene lavas characterized by most radiogenic Hf and Nd isotope ratios, have high Zr/Hf, low Lu/Hf, and little or no Hf anomaly. An appropriate working petrogenetic model is that the Middle Miocene lavas were derived from asthenospheric depleted mantle, slightly ( < 1%) contaminated by slab melt accompanied by full dissolution of zircon. All the Late Miocene and Pliocene samples are characterized by distinctly more radiogenic 176Hf/177Hf and 143Nd/144Nd, and more negative Hf anomalies (greater Hf/Hf* variability; ˜0.3). The Pliocene samples are displaced toward lower Hf/Hf* and Zr/Hf, and higher Lu/Hf relative to the Middle Miocene samples, which requires mixing between depleted mantle and a partial melt of subducted metasediment saturated with trace quantity of zircon.

Early differentiation of the Earth and the Moon.

PubMed

Bourdon, Bernard; Touboul, Mathieu; Caro, Guillaume; Kleine, Thorsten

2008-11-28

We examine the implications of new 182W and 142Nd data for Mars and the Moon for the early evolution of the Earth. The similarity of 182W in the terrestrial and lunar mantles and their apparently differing Hf/W ratios indicate that the Moon-forming giant impact most probably took place more than 60Ma after the formation of calcium-aluminium-rich inclusions (4.568Gyr). This is not inconsistent with the apparent U-Pb age of the Earth. The new 142Nd data for Martian meteorites show that Mars probably has a super-chondritic Sm/Nd that could coincide with that of the Earth and the Moon. If this is interpreted by an early mantle differentiation event, this requires a buried enriched reservoir for the three objects. This is highly unlikely. For the Earth, we show, based on new mass-balance calculations for Nd isotopes, that the presence of a hidden reservoir is difficult to reconcile with the combined 142Nd-143Nd systematics of the Earth's mantle. We argue that a likely possibility is that the missing component was lost during or prior to accretion. Furthermore, the 142Nd data for the Moon that were used to argue for the solidification of the magma ocean at ca 200Myr are reinterpreted. Cumulate overturn, magma mixing and melting following lunar magma ocean crystallization at 50-100Myr could have yielded the 200Myr model age.

Formation and metasomatism of continental lithospheric mantle in intra-plate and subduction-related tectonic settings

NASA Astrophysics Data System (ADS)

Ionov, Dmitri

2010-05-01

Our knowledge of the origin and evolution of the continental lithospheric mantle (CLM) remains fragmentary and partly controversial in spite of recent advances in petrologic, geochemical and geophysical studies of the deep Earth and experimental work. Debate continues on a number of essential topics, like relative contributions of partial melting, metasomatism and ‘re-fertilisation' as well as the timing, conditions and tectonic settings of those processes. These topics can be addressed by studies of ultramafic xenoliths in volcanic rocks which arguably provide the least altered samples of modern and ancient CLM. The subcontinental lithosphere is thought to be a mantle region from which melts have been extracted, thus making the lithosphere more refractory. Melting degrees can be estimated from Al contents while the depth of melt extraction can be assessed from Al-Fe (Mg#) relations in unmetasomatized melting residues in comparison with experimental data, e.g. [1]. High silica and opx in the residues may indicate melting in water-rich conditions. High-precision Mg# and Mn for olivine may constrain degrees and conditions of partial melting and/or metasomatism, tectonic settings, modal compositions (e.g. presence of garnet) and equilibration conditions of mantle peridotites [2]. These estimates require both adequate sampling and high-quality major element and modal data; sampling and analytical uncertainties in published work may contribute substantially to chemical heterogeneities (and different origins) inferred for CLM domains [3]. Very fertile peridotite xenolith suites are rare worldwide [3]. They were initially viewed as representing mantle domains that experienced only very small degrees of melt extraction but are attributed by some workers to ‘refertilization' of refractory mantle by percolating asthenospheric melts. Such alternative mechanisms might be valid for some rare hybrid and Fe-enriched peridotites but they fail to comprehensively explain modal, major and trace element and isotope compositions of fertile lherzolites and thus cannot provide viable alternatives to the concept of melt extraction from pristine mantle as the major mechanism of CLM formation. Published data on xenoliths from andesitic volcanoes and on supra-subduction oceanic peridotites [4] show that the most common rocks in mantle wedge lithosphere are highly refractory harzburgites characterized by a combination of variable but generally high modal opx (18-30%) with very low modal cpx (1.5-3%). At a given olivine (or MgO) content, they have higher opx and silica, and lower cpx, Al and Ca contents than normal refractory peridotite xenoliths in continental basalts; the Mg-Si and Al-Si trends in those rocks resemble those in cratonic peridotites. These features may indicate either fluid fluxing during melting in the mantle wedge or selective post-melting metasomatic enrichments in silica to transform some olivine to opx. High oxygen fugacities and radiogenic Os-isotope compositions in those rocks may be related to enrichments by slab-derived fluids, but these features are not always coupled with trace element enrichments or patterns commonly attributed to "subduction zone metasomatism" deduced from studies of arc volcanic rocks and experiments. The valuable insights provided by experimental work and xenolith case studies are difficult to apply to many natural peridotite series because late-stage processes commonly overlap the evidence for initial melting. References: [1] Herzberg C., J. Petrol. 45: 2507 (2004). [2] Ionov D. & Sobolev A., GCA 72 (S1): A410 (2008). [3] Ionov D., Contrib. Miner. Petrol. (2007) [4] Ionov D., J. Petrol. doi: 10.1093/petrology/egp090 (2010)

Early Precambrian mantle derived rocks in the southern Prince Charles Mountains, East Antarctica: age and isotopic constraints

USGS Publications Warehouse

Mikhalsky, E.V.; Henjes-Kunst, F.; Roland, N.W.

2007-01-01

Mafic and ultramafic rocks occurring as lenses, boudins, and tectonic slabs within metamorphic units in the southern Mawson Escarpment display mantle characteristics of either a highly enriched, or highly depleted nature. Fractionation of these mantle rocks from their sources may be as old as Eoarchaean (ca 3850 Ma) while their tectonic emplacement probably occurred prior to 2550 Ma (U-Pb SHRIMP data). These results provide for the first time evidence for Archaean suturing within East Antarctica. Similar upper mantle sources are likely present in the northern Mawson Escarpment. A younger age limit of these rocks is 2200 Ma, as indicated by presumably metamorphic zircon ages while their magmatic age may be constrained by single zircon dates at 2450-2250 Ma. The area of the northern Mawson Escarpment is most likely of ensimatic origin and includes mafic rocks which were derived from distinct mantle source(s) during Palaeoproterozoic time.

Worldwide occurrence of silica-rich melts in sub-continental and sub-oceanic mantle minerals

NASA Astrophysics Data System (ADS)

Schiano, P.; Clocchiatti, R.

1994-04-01

ROCK samples derived from the Earth's upper mantle commonly show indirect evidence for chemical modification. Such modification, or 'metasomatism', can be recognized by the precipitation of exotic minerals such as phlogopite, amphibole or apatite1, and by the overprinting of the bulk compositions of the mantle rocks by a chemical signature involving the enrichment of potassium and other 'incompatible' elements2. Here we study the composition of the metasomatic agents more directly by examining melt and fluid inclusions trapped in mantle minerals. These inclusions are secondary, forming trails along healed fracture planes. A systematic study of the chemical compositions and entrapment temperatures and pressures of inclusions from 14 ultramaflc peridotites from both continental and oceanic intraplate regions shows that volatile- and silica-rich metasomatic melts are present throughout the litho-sphere. Their compositions, which differ dramatically from those of erupted, mantle-derived magmas, are more akin to continental than to oceanic crust.

Unexpected HIMU-type late-stage volcanism on the Walvis Ridge

NASA Astrophysics Data System (ADS)

Homrighausen, S.; Hoernle, K.; Geldmacher, J.; Wartho, J.-A.; Hauff, F.; Portnyagin, M.; Werner, R.; van den Bogaard, P.; Garbe-Schönberg, D.

2018-06-01

Volcanic activity at many oceanic volcanoes, ridges and plateaus often reawakens after hiatuses of up to several million years. Compared to the earlier magmatic phases, this late-stage (rejuvenated/post-erosional) volcanism is commonly characterized by a distinct geochemical composition. Late-stage volcanism raises two hitherto unanswered questions: Why does volcanism restart after an extended hiatus and what is the origin of this volcanism? Here we present the first 40Ar/39Ar age and comprehensive trace element and Sr-Nd-Pb-Hf isotopic data from seamounts located on and adjacent to the Walvis Ridge in the South Atlantic ocean basin. The Walvis Ridge is the oldest submarine part of the Tristan-Gough hotspot track and is famous as the original type locality for the enriched mantle one (EM I) end member. Consistent with the bathymetric data, the age data indicates that most of these seamounts are 20-40 Myr younger than the underlying or nearby Walvis Ridge basement. The trace element and isotope data reveal a distinct compositional range from the EM I-type basement. The composition of the seamounts extend from the St. Helena HIMU (high time-integrated 238U/204Pb mantle with radiogenic Pb isotope ratios) end member to an enriched (E) Mid-Ocean-Ridge Basalt (MORB) type composition, reflecting a two-component mixing trend on all isotope diagrams. The EMORB end member could have been generated through mixing of Walvis Ridge EM I with normal (N) MORB source mantle, reflecting interaction of Tristan-Gough (EM I-type) plume melts with the upper mantle. The long volcanic quiescence and the HIMU-like geochemical signature of the seamounts are unusual for classical hotspot related late-stage volcanism, indicating that these seamounts are not related to the Tristan-Gough hotspot volcanism. Two volcanic arrays in southwestern Africa (Gibeon-Dicker Willem and Western Cape province) display similar ages to the late-stage Walvis seamounts and also have HIMU-like compositions, suggesting a larger-scale event at ∼77-49 Ma. We propose that the EM I-like mantle plumes rise from the edges of the African Large Low Shear Velocity Province (LLSVP; Tristan-Gough, Discovery and Shona hotspot), whereas the HIMU-dominated intraplate lavas (St. Helena, Gibeon-Dicker Willem and Western Cape province) and the late-stage Walvis seamounts tap material from internal portions of the African LLSVP, suggesting possible lateral and/or vertical chemical zonation of the African LLSVP.

Geochemical evidence for Late Cretaceous marginal arc-to-backarc transition in the Sabzevar ophiolitic extrusive sequence, northeast Iran

NASA Astrophysics Data System (ADS)

Khalatbari Jafari, Morteza; Babaie, Hassan A.; Gani, Moslem

2013-07-01

The ophiolitic extrusive sequence, exposed in an area north of Sabzevar, has three major parts: a lower part, with abundant breccia, hyaloclastic tuff, and sheet flow, a middle part with vesicular, aphyric pillow lava, and an upper part with a sequence of lava and volcanic-sedimentary rocks. Pelagic limestone interlayers contain Late Cretaceous (Maastrichtian-Late Maastrichtian) microfauna. The supra-ophiolitic series includes a sequence of turbidititic and volcanic-sedimentary rocks with lava flow, aphyric and phyric lava, and interlayers of pelagic limestone and radiolarian chert. Paleontological investigation of the pelagic limestone and radiolarite interlayers in this series gives a Late Cretaceous age, supporting the idea that the supra-ophiolitic series formed in a trough, synchronous with the Sabzevar oceanic crust during the Late Cretaceous. Geochemical data indicate a relationship between lava in the upper part of the extrusive sequence and lava in the supra-ophiolitic series. These lavas have a calc-alkaline to almost alkaline characteristic, and show a clear depletion in Nb and definite depletions in Zr and Ti in spider diagrams. Data from these rocks plot in the subduction zone field in tectonomagmatic diagrams. The concentration and position of the heavy rare earth elements in the spider diagrams, and their slight variation, can be attributed to partial melting of the depleted mantle wedge above the subducted slab, and enrichment in the LILE can be attributed to subduction components (fluid, melt) released from the subducting slab. In comparison, the sheet flow and pillow lava of the lower and middle parts of the extrusive sequence show OIB characteristics and high potassium magmatic and shoshonitic trends, and their spider diagram patterns show Nb, Zr, and Ti depletions. The enrichment in the LILE in the spider diagram patterns suggest a low rate of partial melting of an enriched, garnet-bearing mantle. It seems that the marginal arc basin, in which the Sabzevar ophiolite was forming, experienced lithospheric extension in response to slab rollback. This process, which formed a backarc basin, may have aborted the embryonic arc, stopped arc magmatism, and led to the rise of mantle diapirs. The extrusive ophiolite sequence, north of Sabzevar probably formed during the transition from a marginal arc basin to a backarc basin during the Late Cretaceous.

Incorporation of high amounts of Na in ringwoodite: Possible implications for transport of alkali into lower mantle

DOE PAGES

Bindi, Luca; Tamarova, Anastasia; Bobrov, Andrey V.; ...

2016-02-02

In this study, we report on the coexistence between Na-rich ringwoodite and bridgmanite in the system MgSiO 3-Na 2CO 3-Al 2O 3 at 24 GPa and 1700 °C. In our experiments ringwoodite incorporates up to 4.4 wt% Na 2O, with Na entering the octahedral site together with Si, according to the mechanism: Mg 2+ → 2/3Na + + 1/3Si 4+. The volume of the unit cell increases along with the Na content. A similar behavior is observed for the unit-cell volume of Na-bearing bridgmanite, although the mechanism of Na incorporation into this structure remains unknown because of the lack ofmore » sufficient crystallographic data. Na 2O is compatible in ringwoodite relative to bridgmanite with a partition coefficient (D) of 5 (+5/-4), but is incompatible in ringwoodite relative to carbonate-rich melt/fluid, with the D value ranging between 0.5 and 0.1. Al is highly enriched in bridgmanite relative to the other coexisting phases. Carbonatitic melt metasomatism in the deep transition zone may lead to local Na-enrichment, and ringwoodite may be an important host for Na in the deep transition zone. Subsequent convection or subduction of metasomatized mantle may lead to enrichment of alkaline elements in the upper and lower mantle.« less

Water Distribution in the Continental and Oceanic Upper Mantle

NASA Technical Reports Server (NTRS)

Peslier, Anne H.

2015-01-01

Nominally anhydrous minerals such as olivine, pyroxene and garnet can accommodate tens to hundreds of ppm H2O in the form of hydrogen bonded to structural oxygen in lattice defects. Although in seemingly small amounts, this water can significantly alter chemical and physical properties of the minerals and rocks. Water in particular can modify their rheological properties and its distribution in the mantle derives from melting and metasomatic processes and lithology repartition (pyroxenite vs peridotite). These effects will be examined here using Fourier transform infrared spectrometry (FTIR) water analyses on minerals from mantle xenoliths from cratons, plume-influenced cratons and oceanic settings. In particular, our results on xenoliths from three different cratons will be compared. Each craton has a different water distribution and only the mantle root of Kaapvaal has evidence for dry olivine at its base. This challenges the link between olivine water content and survival of Archean cratonic mantle, and questions whether xenoliths are representative of the whole cratonic mantle. We will also present our latest data on Hawaii and Tanzanian craton xenoliths which both suggest the intriguing result that mantle lithosphere is not enriched in water when it interacts with melts from deep mantle upwellings (plumes).

Ridge suction drives plume-ridge interactions

NASA Astrophysics Data System (ADS)

Niu, Y.; Hékinian, R.

2003-04-01

Deep-sourced mantle plumes, if existing, are genetically independent of plate tectonics. When the ascending plumes approach lithospheric plates, interactions between the two occur. Such interactions are most prominent near ocean ridges where the lithosphere is thin and the effect of plumes is best revealed. While ocean ridges are mostly passive features in terms of plate tectonics, they play an active role in the context of plume-ridge interactions. This active role is a ridge suction force that drives asthenospheric mantle flow towards ridges because of material needs to form the ocean crust at ridges and lithospheric mantle in the vicinity of ridges. This ridge suction force increases with increasing plate separation rate because of increased material demand per unit time. As the seismic low-velocity zone atop the asthenosphere has the lowest viscosity that increases rapidly with depth, the ridge-ward asthenospheric flow is largely horizontal beneath the lithosphere. Recognizing that plume materials have two components with easily-melted dikes/veins enriched in volatiles and incompatible elements dispersed in the more refractory and depleted peridotitic matrix, geochemistry of some seafloor volcanics well illustrates that plume-ridge interactions are consequences of ridge-suction-driven flow of plume materials, which melt by decompression because of lithospheric thinning towards ridges. There are excellent examples: 1. The decreasing La/Sm and increasing MgO and CaO/Al_2O_3 in Easter Seamount lavas from Salas-y-Gomez Islands to the Easter Microplate East rift zone result from progressive decompression melting of ridge-ward flowing plume materials. 2. The similar geochemical observations in lavas along the Foundation hotline towards the Pacific-Antarctic Ridge result from the same process. 3. The increasing ridge suction force with increasing spreading rate explains why the Iceland plume has asymmetric effects on its neighboring ridges: both topographic and geochemical anomalies extend < 400 km along the slower (20 to 13 mm/yr northward) spreading South Kolbeinsey Ridge, but > 1500 km along the faster (20 to 25 mm/yr southward) spreading Reykjanes Ridge. 4. The spreading-rate dependent ridge suction force also explains the first-order differences between the fast-spreading East Pacific Rise (EPR) and the slow-spreading Mid-Atlantic Ridge (MAR). Identified mantle plumes/hotspots are abundant near the MAR (e.g., Iceland, Azores, Ascension, Tristan, Gough, Shona and Bouvet), but rare along the entire EPR (notably, the Easter hotspot at ˜27^oS on the Nazca plate). Such apparent unequal hotspot distribution would allow a prediction of more enriched MORB at the MAR than at the EPR. However, the mean compositions between MAR-MORB and EPR-MORB are the same in terms of incompatible element abundances, and are identical in terms of Sr-Nd-Pb isotopic ratios. This suggests similar extents of mantle plume contributions to EPR and MAR MORB. We consider that the apparent rarity of near-EPR plumes/hotspots results from fast spreading. The fast spreading creates large ridge suction forces that do not allow the development of surface expressions of mantle plumes as such, but draw plume materials to a broad zone of sub-ridge upwelling, giving rise to random distribution of abundant enriched MORB and elevated and smooth axial topography along the EPR (vs. MAR). One of the important implications is that the asthenospheric flow is necessarily decoupled from its overlaying oceanic lithospheric plate. This decoupling increases with increasing spreading rate.

Geochemical Variation of Subducting Pacific Crust Along the Izu-Bonin Arc System and its Implications on the Generation of Arc Magmas

NASA Astrophysics Data System (ADS)

Durkin, K.; Castillo, P.; Abe, N.; Kaneko, R.; Straub, S. M.; Garcia, E. S. M.; Yan, Q.; Tamura, Y.

2015-12-01

Subduction zone magmatism primarily occurs due to flux melting of the mantle wedge that has been metasomatized by the slab component. The latter is enriched in volatiles and fluid-mobile elements and derived mainly from subducted sediments and altered oceanic crust (AOC). Subduction input has been linked to arc output in many studies, but this relationship is especially well documented in sedimented arc-trench systems. However, the Izu-Bonin system is sediment-poor, therefore the compositional and latitudinal variations (especially in Pb isotopes) of its arc magmas must be sourced from the subduction component originating primarily from the AOC. Pb is a very good tracer of recycled AOC that may contribute 50% or more of arc magma Pb. Izu-Bonin arc chemistry suggests a subduction influx of Indian-type crust, but the subducting crust sampled at ODP Site 1149 is Pacific-type. The discrepancy between subduction input and arc output calls into question the importance of the AOC as a source of the subduction component, and raises major concerns with our understanding of slab input. During the R/V Revelle 1412 cruise in late 2014, we successfully dredged vertical fault scarps at several sites from 27.5 N to 34.5 N, spanning a range of crustal ages that include a suggested compositional change at ~125 Ma. Major element data show an alkali enrichment towards the north of the study transect. Preliminary incompatible trace element data (e.g. Ba, Zr and Sr) data support this enrichment trend. Detailed mass balance calculations supported by Sr, Nd, Hf and especially Pb isotope analyses will be performed to evaluate whether the AOC controls the Pb isotope chemistry of the Izu-Bonin volcanic arc.

Fluorine and chlorine in mantle minerals and the halogen budget of the Earth's mantle

NASA Astrophysics Data System (ADS)

Urann, B. M.; Le Roux, V.; Hammond, K.; Marschall, H. R.; Lee, C.-T. A.; Monteleone, B. D.

2017-07-01

The fluorine (F) and chlorine (Cl) contents of arc magmas have been used to track the composition of subducted components, and the F and Cl contents of MORB have been used to estimate the halogen content of depleted MORB mantle (DMM). Yet, the F and Cl budget of the Earth's upper mantle and their distribution in peridotite minerals remain to be constrained. Here, we developed a method to measure low concentrations of halogens (≥0.4 µg/g F and ≥0.3 µg/g Cl) in minerals by secondary ion mass spectroscopy. We present a comprehensive study of F and Cl in co-existing natural olivine, orthopyroxene, clinopyroxene, and amphibole in seventeen samples from different tectonic settings. We support the hypothesis that F in olivine is controlled by melt polymerization, and that F in pyroxene is controlled by their Na and Al contents, with some effect of melt polymerization. We infer that Cl compatibility ranks as follows: amphibole > clinopyroxene > olivine orthopyroxene, while F compatibility ranks as follows: amphibole > clinopyroxene > orthopyroxene ≥ olivine, depending on the tectonic context. In addition, we show that F, Cl, Be and B are correlated in pyroxenes and amphibole. F and Cl variations suggest that interaction with slab melts and fluids can significantly alter the halogen content of mantle minerals. In particular, F in oceanic peridotites is mostly hosted in pyroxenes, and proportionally increases in olivine in subduction-related peridotites. The mantle wedge is likely enriched in F compared to un-metasomatized mantle, while Cl is always low (<1 µg/g) in all tectonic settings studied here. The bulk anhydrous peridotite mantle contains 1.4-31 µg/g F and 0.14-0.38 µg/g Cl. The bulk F content of oceanic-like peridotites (2.1-9.4 µg/g) is lower than DMM estimates, consistent with F-rich eclogite in the source of MORB. Furthermore, the bulk Cl budget of all anhydrous peridotites studied here is lower than previous DMM estimates. Our results indicate that nearly all MORB may be somewhat contaminated by seawater-rich material and that the Cl content of DMM could be overestimated. With this study, we demonstrate that the halogen contents of natural peridotite minerals are a unique tool to understand the cycling of halogens, from ridge settings to subduction zones.

Evidence against a chondritic Earth.

PubMed

Campbell, Ian H; O'Neill, Hugh St C

2012-03-28

The (142)Nd/(144)Nd ratio of the Earth is greater than the solar ratio as inferred from chondritic meteorites, which challenges a fundamental assumption of modern geochemistry--that the composition of the silicate Earth is 'chondritic', meaning that it has refractory element ratios identical to those found in chondrites. The popular explanation for this and other paradoxes of mantle geochemistry, a hidden layer deep in the mantle enriched in incompatible elements, is inconsistent with the heat flux carried by mantle plumes. Either the matter from which the Earth formed was not chondritic, or the Earth has lost matter by collisional erosion in the later stages of planet formation.

Re-Os systematics of early proterozoic ferropicrites, Pechenga Complex, northwestern Russia: Evidence for ancient 187Os-enriched plumes

NASA Astrophysics Data System (ADS)

Walker, Richard J.; Morgan, John W.; Hanski, Eero J.; Smolkin, Valery F.

1997-08-01

The Re-Os isotopic systematics of various ferropicritic flows and sills of the Pechenga Complex, Russia, have been examined. During crystallization about 1.98 Ga ago, many of these bodies became highly differentiated. In addition, some of the larger igneous units are associated with major NiCu ore deposits. The melts that produced these rocks have been termed ferropicritic because of their high FeO and MgO contents. They are also enriched in light rare earth elements (LREEs), TiO 2, Zr, and many other incompatible trace elements. Previous studies have concluded that the ferropicrites were most likely derived from an Fe-rich mantle plume that had a complex history of long-term LREE depletion (initial ɛNd = + 1.4), but that also experienced a LREE enrichment event within 200 Ma of the generation of the rocks. Whole rock samples believed to be most representative of primary melt compositions indicate that initial melt concentrations of rhenium and osmium were approximately 1.1 ppb and 0.5 ppb, respectively. The high primary melt concentrations presumably made the osmium contained in the melts relatively immune to the effects of crustal contamination. Nonetheless, all ore-bearing intrusions examined show osmium isotopic evidence for crustal contamination. For example, the initial γOs for some primary magmatic sulfides from the Pilgujärvi intrusion average +46. Other ore-bearing intrusions, such as the Kammikivi sill, appear to have been similarly contaminated by crustal osmium during the injection of magma, with initial yo, values as high as +251. The seemingly high levels of crustal osmium may be attributed to the rapidly diminishing concentrations of osmium in the melts as the larger bodies differentiated, combined with localized in situ assimilation of the metasedimentary rocks that comprise the country rocks. The Re-Os systematics of some whole rock samples of both mineralized and sulfide-poor intrusions were affected by post-magmatic events, especially the greenschist grade metamorphism that impacted the rocks between about 1.7 and 1.8 Ga ago. The metamorphic effects are reflected in the recrystallization of many of the primary sulfides. As a consequence of this open-system behavior in many whole rock samples, the primary igneous Re-Os systematics of these rocks are best examined via analysis of magmatic phases such as chromite, olivine, clinopyroxene, and primary sulfides. Chromite and ilmenite+sulfide separates from two sulfide-poor lava flows, the Lammas and Keskitunturi, have characteristically low 187Re/ 188Os ( < l), and because of the limited age correction, precisely define the initial γOs of these systems to be +6.0±0.7. Because of the identical initial compositions of the two, spatially distinct lava flows, and the fact that these flows were extruded onto only slightly older volcanic rocks, we conclude that the +6.0 value reflects the composition of the mantle source and not minor crustal contamination. Although 187Os-enriched, plume-derived systems are common during the Phanerozoic, this is the earliest known evidence for the existence of long-term, Re-enriched mantle reservoirs. The most commonly invoked model to explain 187Os enrichments in Phanerozoic systems, oceanic crustal recycling, in this instance requires that very large proportions of oceanic crust were recycled into the mantle source and that the event was likely very ancient. Other options, such as core-mantle interaction and a stratified mantle, are also discussed.

Boron isotopic composition of olivine-hosted melt inclusions from Gorgona komatiites, Colombia: New evidence supporting wet komatiite origin

NASA Astrophysics Data System (ADS)

Gurenko, Andrey A.; Kamenetsky, Vadim S.

2011-12-01

A fundamental question in the genesis of komatiites is whether these rocks originate from partial melting of dry and hot mantle, 400-500 °C hotter than typical sources of MORB and OIB magmas, or if they were produced by hydrous melting of the source at much lower temperatures, similar or only moderately higher than those known today. Gorgona Island, Colombia, is a unique place where Phanerozoic komatiites occur and whose origin is directly connected to the formation of the Caribbean Large Igneous Province. The genesis of Gorgona komatiites remains controversial, mostly because of the uncertain origin of volatile components which they appear to contain. These volatiles could equally result from shallow level magma contamination, melting of a "damp" mantle or fluid-induced partial melting of the source due to devolatilization of the ancient subducting plate. We have analyzed boron isotopes of olivine-hosted melt inclusions from the Gorgona komatiites. These inclusions are characterized by relatively high contents of volatile components and boron (0.2-1.0 wt.% H 2O, 0.05-0.08 wt.% S, 0.02-0.03 wt.% Cl, 0.6-2.0 μg/g B), displaying positive anomalies in the overall depleted, primitive mantle (PM) normalized trace element and REE spectra ([La/Sm] n = 0.16-0.35; [H 2O/Nb] n = 8-44; [Cl/Nb] n = 27-68; [B/Nb] n = 9-30, assuming 300 μg/g H 2O, 8 μg/g Cl and 0.1 μg/g B in PM; Kamenetsky et al., 2010. Composition and temperature of komatiite melts from Gorgona Island constrained from olivine-hosted melt inclusions. Geology 38, 1003-1006). The inclusions range in δ11B values from - 11.5 to + 15.6 ± 2.2‰ (1 SE), forming two distinct trends in a δ11B vs. B-concentration diagram. Direct assimilation of seawater, seawater-derived components, altered oceanic crust or marine sediments by ascending komatiite magma cannot readily account for the volatile contents and B isotope variations. Alternatively, injection of < 3wt.% of a 11B enriched fluid to the mantle source could be a plausible explanation for the δ11B range that also may explain the H 2O, Cl and B excess.

Mantle upwelling and trench-parallel mantle flow in the northern Cascade arc indicated by basalt geochemistry

NASA Astrophysics Data System (ADS)

Mullen, E.; Weis, D.

2013-12-01

Cascadia offers a unique perspective on arc magma genesis as an end-member ';hot' subduction zone in which relatively little water may be available to promote mantle melting. The youngest and hottest subducting crust (~5 Myr at the trench) occurs in the Garibaldi Volcanic Belt, at the northern edge of the subducting Juan de Fuca plate [1]. Geochemical data from GVB primitive basalts provide insights on mantle melting where a slab edge coincides with high slab temperatures. In subduction zones worldwide, including the Cascades, basalts are typically calc-alkaline and produced from a depleted mantle wedge modified by slab input. However, basalts from volcanic centers overlying the northern slab edge (Salal Glacier and Bridge River Cones) are alkalic [2] and lack a trace element subduction signature [3]. The mantle source of the alkalic basalts is significantly more enriched in incompatible elements than the slab-modified depleted mantle wedge that produces calc-alkaline basalts in the southern GVB (Mt. Baker and Glacier Peak) [3]. The alkalic basalts are also generated at temperatures and pressures of up to 175°C and 1.5 GPa higher than those of the calc-alkaline basalts [3], consistent with decompression melting of fertile, hot mantle ascending through a gap in the Nootka fault, the boundary between the subducting Juan de Fuca plate and the nearly stagnant Explorer microplate. Mantle upwelling may be related to toroidal mantle flow around the slab edge, which has been identified in southern Cascadia [4]. In the GVB, the upwelling fertile mantle is not confined to the immediate area around the slab edge but has spread southward along the arc axis, its extent gradually diminishing as the slab-modified depleted mantle wedge becomes dominant. Between Salal Glacier/Bridge River and Glacier Peak ~350 km to the south, there are increases in isotopic ratios (ɛHf = 8.3 to13.0, ɛNd = 7.3 to 8.5, and 208Pb*/206*Pb* = 0.914 to 0.928) and trace element indicators of slab input (e.g., Ba/Nb, Ba/La), along with a transition of basalt compositions from alkalic to calc-alkaline [2]. Mantle upwelling at slab edges and arc-parallel mantle flow are recognized in an increasing number of subduction zones from seismic anisotropy data [5]. In the GVB, the geochemical evidence for these phenomena is reinforced by shear-wave splitting measurements indicating complex mantle flow around the northern Cascadia slab edge [6]. The influx of enriched asthenosphere into the northern Cascadia mantle wedge accounts for why GVB basalts display compositional differences from other Cascade arc basalts. [1] Wilson (2002) USGS Open-File Rep 02-328; [2] Green (2006) Lithos 86, 23; [3] Mullen & Weis (2013) Geochem Geophys Geosys, in press; [4] Zandt & Humphreys (2008) Geology 36, 295; [5] Long & Silver (2008) Science 319, 315; [6] Currie et al. [2004] Geophys J Int 157, 341.

On the nature of the Ni-rich component in splash-form Australasian tektites

NASA Astrophysics Data System (ADS)

Goderis, Steven; Tagle, Roald; Fritz, Jörg; Bartoschewitz, Rainer; Artemieva, Natalia

2017-11-01

The Australasian tektite strewn field is exceptional, not only as the largest and most recent, but also as the only strewn field without an identified source impact crater. Therefore, scenarios without the formation of an impact crater, such as a low altitude cometary airburst, have proven hard to discard. Here, new geochemical evidence is presented for mixing of projectile and target material, which implies the formation of an Australasian tektite-related impact crater. First, ninety-two Australasian tektites were grouped according to their Cr, Co and Ni concentrations. Based on this data, Australasian tektites with the highest Ni contents (>200 μg/g) occur more than 1500 km south-southeast (SSE) of the northern Indochina region, with the highest concentration of Ni-rich tektites in South Vietnam, the islands of Borneo, Belitung, and Java, and reports in literature for Ni-rich tektites in central Australia. The tektites with the highest Cr and Ni abundances often also show highly siderophile element (HSE) enrichments of up to 4 ng/g Ir. The most Ni-rich samples exhibit broadly chondrite-relative HSE proportions. However, a chondritic impactor contribution appears to be inconsistent with the observed Ni/Cr, Ni/Co, and Cr/Co ratios. A previously suggested significant terrestrial mantle contribution can also not explain the siderophile element enrichments in combination with relatively low FeOtot (<7 wt.%) and MgO (<4 wt.%) contents. Elemental fractionation during impact cratering or tektite formation by an impactor with a chondritic signature may explain these observations. Alternatively, a projectile component from a primitive achondrite may be advocated, with contribution from a mafic to ultramafic extraterrestrial lithology with a relatively unfractionated HSE signature and Ni/Cr ratio distinctly higher than those of Earth's mantle. Element distribution maps obtained from individual Australasian tektites document complex mingling processes of chemically distinct melt batches, each exhibiting variable contributions from distinct endmember compositions. These texturally recorded mingling processes are consistent with high-resolution numerical models of impact cratering processes that resolve the growth of Kelvin-Helmholtz instabilities at the projectile/target interface during impact, when both materials co-occur at high pressure. These numerical models indicate that Ni-rich tektite populations across the central part of the Australasian tektite strewn field could represent projectile-enriched material preferentially ejected downrange. Continued tracing of this Ni-rich component across the strewn field may help to constrain the location of the yet to be identified source crater of the Australasian (micro)tektites.

Tin isotope fractionation during magmatic processes and the isotope composition of the bulk silicate Earth

NASA Astrophysics Data System (ADS)

Wang, Xueying; Amet, Quentin; Fitoussi, Caroline; Bourdon, Bernard

2018-05-01

Tin is a moderately volatile element whose isotope composition can be used to investigate Earth and planet differentiation and the early history of the Solar System. Although the Sn stable isotope composition of several geological and archaeological samples has been reported, there is currently scarce information about the effect of igneous processes on Sn isotopes. In this study, high-precision Sn isotope measurements of peridotites and basalts were obtained by MC-ICP-MS with a double-spike technique. The basalt samples display small variations in δ124/116Sn ranging from -0.01 ± 0.11 to 0.27 ± 0.11‰ (2 s.d.) relative to NIST SRM 3161a standard solution, while peridotites have more dispersed and more negative δ124Sn values ranging from -1.04 ± 0.11 to -0.07 ± 0.11‰ (2 s.d.). Overall, basalts are enriched in heavy Sn isotopes relative to peridotites. In addition, δ124Sn in peridotites become more negative with increasing degrees of melt depletion. These results can be explained by different partitioning behavior of Sn4+ and Sn2+ during partial melting. Sn4+ is overall more incompatible than Sn2+ during partial melting, resulting in Sn4+-rich silicate melt and Sn2+-rich residue. As Sn4+ has been shown experimentally to be enriched in heavy isotopes relative to Sn2+, the effect of melting is to enrich residual peridotites in relatively more compatible Sn2+, which results in isotopically lighter peridotites and isotopically heavier mantle-derived melts. This picture can be disturbed partly by the effect of refertilization. Similarly, the presence of enriched components such as recycled oceanic crust or sediments could explain part of the variations in Sn isotopes in oceanic basalts. The most primitive peridotite analyzed in this study was used for estimating the Sn isotope composition of the BSE, with δ124Sn = -0.08 ± 0.11‰ (2 s.d.) relative to the Sn NIST SRM 3161a standard solution. Altogether, this suggests that Sn isotopes may be a powerful probe of redox processes in the mantle.

The Complex History of Alarcon Rise Mid-Ocean Ridge Rhyolite Revealed through Mineral Chemistry

NASA Astrophysics Data System (ADS)

Dreyer, B. M.; Portner, R. A.; Clague, D. A.; Daczko, N. R.; Castillo, P.; Bindeman, I. N.

2014-12-01

A suite of basalts to rhyolites recovered from the Alarcon Rise, the northern extension of the intermediate spreading-rate East Pacific Rise, provides an unparalleled test of established mechanisms for high-Si lava formation at ridges. Rhyolites are ≤35% phyric and poorly vesicular. Mafic xenoclasts are common, and plagioclase is the dominant phase. Olivine and clinopyroxene are also common, and orthopyroxene, FeTi-oxides, zircon, and rare pyrite blebs are present. Major and trace element glass data are consistent with MELTS models of fractional crystallization from a parental melt, but a diverse mineral population records added complexity. Olivine and plagioclase compositions are broadly consistent with models, with the exception of more variable Fo52-77 and An87-28 in a basaltic andesitic composition where pigeonite is predicted to replace olivine in the crystallizing assemblage between ~1085-1015°C; pigeonites analyzed in an andesite have lower Ca and Fe than predicted. Clinopyroxene variability generally increases with host melt SiO2, from Mg# 86-84 in basalts to Mg# 80-21 in rhyolites, and zoning is common with higher-MgO anhedral cores mantled by lower-MgO euhedral rims. Cooler magmas aided the preservation of disequilibrium and are supported by ~715-835°C Ti-in-zircon and ilmenite-magnetite thermometry in rhyolites. Despite a well-predicted liquid line of decent, multiple signals of chemical disequilibrium in intermediate to silicic melts support mixing of magmatic batches and/or assimilation of partially hydrous crust. Assimilation is permissible given δ18O values that are lower than expected solely from fractional crystallization (i.e., <6.3‰ at 77% SiO2), but assimilation extent is limited on the basis of δD ~82±8 and Pacific MORB-like 87Sr/86Sr. Zircon Hf-isotopes and trace element patterns support a juvenile oceanic crustal source. Whereas depleted Pacific MORB mantle source reservoir is supported by whole rock Sr-Nd isotopes, slight enrichments in zircon 176Hf/177Hf and whole rock 207,206Pb/204Pb may indicate an enriched MORB mantle component. In conclusion, mid-ocean rhyolite at Alarcon formed from a variety of petrogenetic processes including magma-mixing, assimilation, and crystallization following partial melting of slightly heterogeneous mantle source(s).

Plunging Plates Cause a Stir.

ERIC Educational Resources Information Center

Weisburd, Stefi

1986-01-01

Reviews current ideas and research findings related to the flow patterns of mantle rocks. Highlights the components of the two-layer convection and whole-mantle models of mantle flow. Proposes that mantle flow is the key to understanding how the earth has cooled and chemically evolved. (ML)

Phase behavior and reactive transport of partial melt in heterogeneous mantle model

NASA Astrophysics Data System (ADS)

Jordan, J.; Hesse, M. A.

2013-12-01

The reactive transport of partial melt is the key process that leads to the chemical and physical differentiation of terrestrial planets and smaller celestial bodies. The essential role of the lithological heterogeneities during partial melting of the mantle is increasingly recognized. How far can enriched melts propagate while interacting with the ambient mantle? Can the melt flow emanating from a fertile heterogeneity be localized through a reactive infiltration feedback in a model without exogenous factors or contrived initial conditions? A full understanding of the role of heterogeneities requires reactive melt transport models that account for the phase behavior of major elements. Previous work on reactive transport in the mantle focuses on trace element partitioning; we present the first nonlinear chromatographic analysis of reactive melt transport in systems with binary solid solution. Our analysis shows that reactive melt transport in systems with binary solid solution leads to the formation of two separate reaction fronts: a slow melting/freezing front along which enthalpy change is dominant and a fast dissolution/precipitation front along which compositional changes are dominated by an ion-exchange process over enthalpy change. An intermediate state forms between these two fronts with a bulk-rock composition and enthalpy that are not necessarily bounded by the bulk-rock composition and enthalpy of either the enriched heterogeneity or the depleted ambient mantle. The formation of this intermediate state makes it difficult to anticipate the porosity changes and hence the stability of reaction fronts. Therefore, we develop a graphical representation for the solution that allows identification of the intermediate state by inspection, for all possible bulk-rock compositions and enthalpies of the heterogeneity and the ambient mantle. We apply the analysis to the partial melting of an enriched heterogeneity. This leads to the formation of moving precipitation front that followes a stationary melting front which creates low porosity intermediate states. Therefore, localization of the melt flow is not observed because the precipitation front is stable and the melting front is always stationary under these conditions. This analysis illustrates the counterintuitive behavior that can arise when the phase behavior is taken into account and is a first step to understanding reactive melt transport and the reactive constraints on channelization in partial melts. ¬¬

New Hafnium Isotope and Trace Element Constraints on the Role of a Plume in Genesis of the Eastern Snake River Plain Basalts, Idaho

NASA Astrophysics Data System (ADS)

Taylor, R. D.; Reid, M. R.; Blichert-Toft, J.

2009-12-01

Bimodal volcanism associated with the eastern Snake River Plain (ESRP)-Yellowstone Plateau province has persisted since approximately 16 Ma. A time-transgressive track of rhyolitic eruptions which young progressively to the east and parallel the motion of the North American plate are overlain by younger basalts with no age progression. Interpretations for the origin of these basalts range from a thermo-chemical mantle plume to incipient melting of the shallow upper mantle, and remain controversial. The enigmatic ESRP basalts are characterized by high 3He/4He, diagnostic of a plume source, but also by lithophile radiogenic isotope signatures that are more enriched than expected for plume-derived OIBs. These features could possibly be caused by isotopic decoupling associated with shallow melting of a hybridized upper mantle, or derivation from an atypical mantle plume, or both by way of mixing. New Hf isotope and trace element data further constrain potential sources for the ESRP basalts. Their Hf isotopic signatures (ɛHf = +0.1 to -5.8) are moderately enriched and consistently fall above or in the upper part of the field of OIBs, with similar Nd isotope signatures (ɛNd = -2.0 to -5.8), indicating a source with high time-integrated Lu/Hf compared with Sm/Nd. The isotopic compositions of the basalts lie between those of Archean SCML and a more depleted end-member source, suggestive of contributions from at least two sources. The grouping of isotopic characteristics is compact compared to other regional volcanism, implying that the hybridization process is highly reproducible within the ESRP. Minor localized differences in isotopic composition may signify local variations in the relative proportions of the end-members. Trace element patterns also support genesis of the ESRP basalts from an enriched source. Our data detect evidence of deeper contributions derived from the garnet-stability field, and a greater affinity of the trace element signatures to plume sources than to sources in the mantle lithosphere. The Hf isotope and trace element characteristics of the ESRP basalts thus support a model of derivation from a deep mantle plume with additional melt contributions and isotopic overprinting from SCML.

Resolving the potential mantle reservoirs that influence volcanism in the West Antarctic Rift System

NASA Astrophysics Data System (ADS)

Maletic, E. L.; Darrah, T.

2017-12-01

Lithospheric extension and magmatism are key characteristics of active continental rift zones and are often associated with long-lasting alkaline magmatic provinces. In these settings, a relationship between lithospheric extension and mantle plumes is often assumed for the forces leading to rift evolution and the existence of a plume is commonly inferred, but typically only extension is supported by geological evidence. A prime example of long-lasting magmatism associated with an extensive area of continental rifting is the West Antarctic Rift System (WARS), a 2000 km long zone of ongoing extension within the Antarctic plate. The WARS consists of high alkaline silica-undersaturated igneous rocks with enrichments in light rare earth elements (LREEs). The majority of previous geochemical work on WARS volcanism has focused on bulk classification, modal mineralogy, major element composition, trace element chemistry, and radiogenic isotopes (e.g., Sr, Nd, and Pb isotopes), but very few studies have evaluated volatile composition of volcanics from this region. Previous explanations for WARS volcanism have hypothesized a plume beneath Marie Byrd Land, decompression melting of a fossilized plume head, decompression melting of a stratified mantle source, and mixing of recycled oceanic crust with one or more enriched mantle sources from the deep mantle, though researchers are yet to reach a consensus. Unlike trace elements and radiogenic isotopes which can be recycled between the crust and mantle and which are commonly controlled by degrees of partial melting and prior melt differentiation, noble gases are present in low concentrations and chemically inert, allowing them to serve as reliable tracers of volatile sources and subsurface processes. Here, we present preliminary noble gas isotope (e.g., 3He/4He, CO2/3He, CH4/3He, 40Ar/36Ar, 40Ar*/4He) data for a suite of lava samples from across the WARS. By coupling major and trace element chemistry with noble gas elemental and isotopic composition and other volatiles from a suite of volcanic rocks in the WARS, we can better constrain a magmatic source and provide geological evidence that could support or oppose the existence of a mantle plume, HIMU plume, or deconvolve mantle-lithosphere interactions.

A Geochemical View on the Interplay Between Earth's Mantle and Crust

NASA Astrophysics Data System (ADS)

Chauvel, C.

2017-12-01

Over most of Earth history, oceanic and continental crust was created and destroyed. The formation of both types of crust involves the crystallization and differentiation of magmas producing by mantle melting. Their destruction proceeds by mechanical erosion and weathering above sea level, chemical alteration on the seafloor, and bulk recycling in subduction zones. All these processes enrich of some chemical element and deplete others but each process has its own effect on chemical elements. While the flux of material from mantle to crust is well understood, the return flux is much more complex. In contrast to mantle processes, erosion, weathering, chemical alteration and sedimentary processes strongly decouple elements such as the rare earths and high-field strength elements due to their different solubilities in surface fluids and mineralogical sorting during transport. Soluble elements such as strontium or uranium are quantitatively transported to the ocean by rivers and decoupled from less soluble elements. Over geological time, such decoupling significantly influences the extent to which chemical elements remain at the Earth's surface or find their way back to the mantle through subduction zones. For example, elements like Hf or Nd are retained in heavy minerals on continents whereas U and Sr are transported to the oceans and then in subduction zones to the mantle. The consequence is that different radiogenic isotopic systems give disparate age estimates for the continental crust; e.g, Hf ages could be too old. In subduction zones, chemical elements are also decoupled, due to contrasting behavior during dehydration or melting in subducting slabs. The material sent back into the mantle is generally enriched in non-soluble elements while most fluid-mobile elements return to the crust. This, in turn, affects the relationship between the Rb-Sr, Sm-Nd, Lu-Hf and U-Th-Pb isotopic systems and creates correlations unlike those based on magmatic processes. By quantifying the difference between isotopic arrays created by magmatic processes vs. surface and subduction processes, we can determine how crust recycling creates isotopic heterogeneities in the mantle.

Recycled oceanic crust in the source of 90-40 Ma basalts in North and Northeast China: Evidence, provenance and significance

NASA Astrophysics Data System (ADS)

Xu, Yi-Gang

2014-10-01

Major, trace element and Sr-Nd-Pb isotopic data of basalts emplaced during 90-40 Ma in the North and Northeast China are compiled in this review, with aims of constraining their petrogenesis, and by inference the evolution of the North China Craton during the late Cretaceous and early Cenozoic. Three major components are identified in magma source, including depleted component I and II, and an enriched component. The depleted component I, which is characterized by relatively low 87Sr/86Sr (<0.7030), moderate 206Pb/204Pb (18.2), moderately high εNd (∼4), high Eu/Eu∗ (>1.1) and HIMU-like trace element characteristics, is most likely derived from gabbroic cumulate of the oceanic crust. The depleted component II, which distinguishes itself by its high εNd (∼8) and moderate 87Sr/86Sr (∼0.7038), is probably derived from a sub-lithospheric ambient mantle. The enriched component has low εNd (2-3), high 87Sr/86Sr (>0.7065), low 206Pb/204Pb (17), excess Sr, Rb, Ba and a deficiency of Zr and Hf relative to the REE. This component is likely from the basaltic portion of the oceanic crust, which is variably altered by seawater and contains minor sediments. Comparison with experimental melts and trace element modeling suggest that these recycled oceanic components may be in form of garnet pyroxenite/eclogite. These components are young (<0.5 Ga) and show an Indian-MORB isotopic character. Given the share of this isotopic affinity by the extinct Izanaghi-Pacific plate, currently stagnated within the mantle transition zone, we propose that it ultimately comes from the subducted Pacific slab. Eu/Eu∗ and 87Sr/86Sr of the 90-40 Ma magmas increases and decreases, respectively, with decreasing emplacement age, mirroring a change in magma source from upper to lower parts of subducted oceanic crust. Such secular trends are created by dynamic melting of a heterogeneous mantle containing recycled oceanic crust. Due to different melting temperature of the upper and lower ocean crust and progressive thinning of the lithosphere, the more fertile basaltic crustal component is preferentially sampled during the early stage of volcanism, whereas the more depleted gabbroic lower crust and lithospheric mantle components are preferentially sampled during a late stage. This model is consistent with a protracted destruction process of the lithosphere beneath eastern China. The presence of significant recycled oceanic crust components in the 90-40 Ma basalts highlights the influence of Pacific subduction on the deep processes in the North China Craton, which can be traced back at least to the late Cretaceous. This, along with the conjugation of crustal deformation pattern in this region with the movement of the Pacific plate, makes the Pacific subduction as a potential trigger of the destruction of the North China Craton. Geophysical investigations and morphological analyses indicate that decratonization is largely confined to east of the NSGL, whereas to west of NSGL, in particular the Ordos basin, characteristics typical of a craton are observed (Menzies et al., 2007; Zhu et al., 2011). This spatial pattern of craton destruction, together with NE-NNE-oriented extensional basins, main structural alignments and metamorphic core complexes (Zheng et al., 1978; Ye et al., 1987; Ren et al., 2002; Liu et al., 2006; Zhu G et al., 2012), is consistent with the subduction direction of the Pacific plate. Two main episodes of late Mesozoic magmatism have been identified in the Jurassic and the early Cretaceous. These correspond to the subduction of the Pacific plate underneath the Eurasian content and to subsequent extensions, respectively (Wu et al., 2005, 2006). Global tomography studies indicate that the subducted Pacific oceanic slab has become stagnant within the mantle transition zone and extended subhorizontally westward beneath the East Asian continent (Fukao et al., 1992; Huang and Zhao, 2006; Chen and Ai, 2009; Van der Hilst and Li, 2010). The western end of this stagnant slab does not go beyond the NNE-trending NSGL (Huang and Zhao, 2006; Xu, 2007). Given the subduction of Pacific plate underneath eastern Asian continent, the slab-derived materials are expected to be involved in the sources of the Mesozoic-Cenozoic magmas in this region. Recent studies have shown the ubiquitous presence of subduction-related components in late Cenozoic basalts in eastern China (Zhang et al., 2009; Xu et al., 2012b; Sakuyama et al., 2013). However, it remains unclear whether similar recycled oceanic components are present in earlier basalts (i.e., those emplaced during 90-40 Ma, Fig. 1), for which high quality geochemical data are not available until very recently (Zhang et al., 2008; Kuang et al., 2012; Xu et al., 2012a). In addition, the provenance of recycled oceanic components, if any, is highly relevant to the proposal of the Pacific subduction as one of the possible triggers of the destruction of the NCC. The timing of the first appearance of oceanic components in magmas will provide constraints on the role of the Pacific subduction on the evolution of the NCC.The objective of this study is to review and compile major, trace elements and Sr-Nd-Pb isotopic compositions of mafic magmas emplaced since 90 Ma in North and Northeastern China, and to use these data to elaborate their petrogenesis. We will demonstrate the ubiquitous involvement of subduction-related components in the magma sources. Furthermore, temporal variation in geochemical features suggests that different parts of the recycled oceanic crust are preferentially sampled at different time. In collaborating with melting solidus temperature and the melting column concept, this is interpreted as differential melting of upwelling heterogeneous mantle as a result of lithospheric thinning. The peculiar isotopic compositions of these oceanic crust components suggests a link with the subducted Pacific slab, which currently stagnates at the mantle transition zone beneath the eastern Asian continental margin (Fukao et al., 1992; Huang and Zhao, 2006). This study therefore provides petrological evidence for the effect of Pacific subduction on the studied region, rendering the Pacific subduction as a potential trigger of the destruction of the NCC.

Rare Mineralogy in Alkaline Ultramafic Rocks, Western Kentucky Fluorspar District

NASA Astrophysics Data System (ADS)

Anderson, W.

2017-12-01

The alkaline ultramafic intrusive dike complex in the Western Kentucky Fluorspar District contains unusual mineralogy that was derived from mantle magma sources. Lamprophyre and peridotite petrologic types occur in the district where altered fractionated peridotites are enriched in Rare Earth Elements (REE) and some lamprophyre facies are depleted in incompatible elements. Unusual minerals in dikes, determined by petrography and X-ray diffraction, include schorlomite and andradite titanium garnets, astrophyllite, spodumene, niobium rutile, wüstite, fluoro-tetraferriphlogopite, villiaumite, molybdenite, and fluocerite, a REE-bearing fluoride fluorescent mineral. Mixing of MVT sphalerite ore fluids accompanies a mid-stage igneous alteration and intrusion event consistent with paragenetic studies. The presence of lithium in the spodumene and fluoro-tetraferriphlogopite suggests a lithium phase in the mineral fluids, and the presence of enriched REE in dikes and fluorite mineralization suggest a metasomatic event. Several of these rare minerals have never been described in the fluorspar district, and their occurrence suggests deep mantle metasomatism. Several REE-bearing fluoride minerals occur in the dikes and in other worldwide occurrences, they are usually associated with nepheline syenite and carbonatite differentiates. There is an early and late stage fluoride mineralization, which accompanied dike intrusion and was also analyzed for REE content. One fluorite group is enriched in LREE and another in MREE, which suggests a bimodal or periodic fluorite emplacement. Whole-rock elemental analysis was chondrite normalized and indicates that some of the dikes are slightly enriched in light REE and show a classic fractionation enrichment. Variations in major-element content; high titanium, niobium, and zirconium values; and high La/Yb, Zr/Y, Zr/Hf, and Nb/Ta ratios suggest metasomatized lithospheric-asthenospheric mantle-sourced intrusions. The high La/Yb ratios in some dikes in the titanium garnet facies suggest a magma melt trend toward the carbonation phase of a fractionated peridotite parent magma.

Petrogenesis of strongly alkaline primitive volcanic rocks at the propagating tip of the western branch of the East African Rift

NASA Astrophysics Data System (ADS)

Rosenthal, A.; Foley, S. F.; Pearson, D. G.; Nowell, G. M.; Tappe, S.

2009-06-01

Strongly silica-undersaturated potassic lavas (kamafugites) and carbonatitic tuffs are characteristic of the Toro-Ankole volcanic field in southwestern Uganda, forming the youngest and most northward volcanics of the western branch of the East African Rift. Lavas contain exceptionally low SiO 2 (31.8-42.8 wt.%), high CaO (up to 16.6 wt.%) and K 2O (up to 7 wt.%). They exhibit moderately enriched correlated Nd ( ɛNd - 0.1 to - 4.7) and Hf ( ɛHf - 0.1 to - 8.8) isotope signatures, indicating time-integrated enrichment in incompatible elements in the source, attributed to mixing between two metasomatic assemblages, a phlogopite-rich MARID-type and a later carbonate-rich assemblage. The restricted range of 87Sr/ 86Sr (0.704599-0.705402) is due to Sr being dominated by the carbonate-rich assemblage, which also imparts a Nd and Hf signature similar to convecting upper mantle. Os isotopes ( γOs up to 290 and variable Os concentrations of 0.056-1.454 ppb) are curved due to mixing between the carbonate-rich metasome and a second end-member that may be derived from melting peridotite, the MARID assemblage, or a mixture of both. Enrichment of the peridotitic mantle in carbonate and silicate melts at 4-6 GPa occurs also in other areas where geochemically similar ultramafic lamprophyres result. The Ugandan kamafugites thus represent the earliest and deepest-derived magmas in a rift through thick continental lithosphere beneath the continuous Congo-Tanzania craton. The Ugandan rift-related mantle enrichment is older than the earliest known tectonic surface expression of the rift.

Nitrogen isotopic components in the early solar system

NASA Technical Reports Server (NTRS)

Kerridge, J. F.

1994-01-01

It is quite common to take the terrestrial atmospheric value of (15)N/(14)N (0.00366) as typical of nitrogen in the early solar system, but in fact there is little reason to suppose that this value had a nebula-wide significance. Indeed, it is not clear that there was a unique solar-system-wide (15)N/(14)N ratio, of whatever value. Here we review what is known about the distribution of the nitrogen isotopes among those solar-system objects that have been sampled so far and conclude that those isotopes reveal widespread inhomogeneity in the early solar system. Whether the isotopically distinct primordial components implied by this analysis were solid or gaseous or a mixture of both is not known. The isotopic composition of N in the Earth's mantle is controversial: estimates range from a 1.1 percent depletion in (15)N to a 1.4 percent enrichment. (Isotopic compositions will be expressed throughout as percent deviations from the terrestrial atmospheric value.) The present-day Martian atmosphere is characterized by a value of plus 62 percent but this enrichment in (15)N is attributed to selective loss of (14)N from the Martian exosphere. Modelling of this fractionation leads to an estimated primordial composition similar to the terrestrial atmospheric value, through the precision of this model-dependent result is unclear.

La Isla de Gorgona, Colombia: A petrological enigma?

NASA Astrophysics Data System (ADS)

Kerr, Andrew C.

2005-09-01

A wide range of intrusive (wehrlite, dunite, gabbro and olivine gabbro) and extrusive (komatiites picrites and basalts) igneous rocks are found on the small pacific island of Gorgona. The island is best known for its ˜90 Ma spinifex-textured komatiites: the only true Phanerozoic komatiites yet discovered. Early work led to suggestions that the rocks of the island formed at a mid-ocean ridge, however more recent research supports an origin as part of a hot mantle plume-derived oceanic plateau. One of the main lines of evidence for this origin stems from the inferred high mantle source temperatures required to form the high-MgO (> 15 wt.%) komatiites and picrites. Another remarkable feature of the island, considering its small size (8 × 2.5 km), is the degree of chemical and radiogenic isotopic heterogeneity shown by the rocks. This heterogeneity requires a mantle source region with at least three isotopically distinctive source regions (two depleted and one enriched). Although these mantle source regions appear to be derived in significant part from recycled oceanic crust and lithosphere, enrichments in 187Os, 186Os and 3He in Gorgona lavas and intrusive rocks, suggest some degree of transfer of material from the outer core to the plume source region at D″. Modelling reveals that the komatiites probably formed by dynamic melting at an average pressure of 3-4 GPa leaving residual harzburgite. Trace element depletion in Gorgona ultramafic rocks appears to be the result of earlier, deeper melting which produced high-MgO trace element-enriched magmas. The discovery of a trace-element enriched picrite on the island has confirmed this model. Gorgona accreted onto the palaeocontinental margin of northwestern South America in the Eocene and palaeomagnetic work reveals that it was formed at ˜26 °S. It has been proposed that Gorgona is a part of the Caribbean-Colombian Oceanic Plateau (CCOP), however, the CCOP accreted in the Late Cretaceous and was derived from a more equatorial palaeolatitude. This evidence, and differing geochemical signatures, strongly suggests that Gorgona and probably other coastal oceanic plateau sequences in Colombia and Ecuador, belong to a completely different oceanic plateau to the CCOP.

Noble gas composition of Indian carbonatites (Amba Dongar, Siriwasan): Implications on mantle source compositions and late-stage hydrothermal processes

NASA Astrophysics Data System (ADS)

Hopp, Jens; Viladkar, Shrinivas G.

2018-06-01

Within a stepwise crushing study we determined the noble gas composition of several calcite separates, one aegirine and one pyrochlore-aegirine separate of the carbonatite ring dyke complex of Amba Dongar and carbonatite sill complex of Siriwasan, India. Both carbonatites are related to the waning stages of volcanic activity of the Deccan Igneous Province ca. 65 Ma ago. Major observations are a clear radiogenic 4He* and nucleogenic 21Ne* imprint related to in situ production from U and Th in mineral impurities, most likely minute apatite grains, or late incorporation of crustal fluids. However, in first crushing steps of most calcites from Amba Dongar a well-resolvable mantle neon signal is observed, with lowest air-corrected mantle 21Ne/22Ne-compositions equivalent to the Réunion hotspot mantle source. In case of the aegirine separate from Siriwasan we found a neon composition similar to the Loihi hotspot mantle source. This transition from a mantle plume signal in first crushing step to a more nucleogenic signature with progressive crushing indicates the presence of an external (crustal) or in situ nucleogenic component unrelated and superposed to the initial mantle neon component whose composition is best approximated by results of first crushing step(s). This contradicts previous models of a lithospheric mantle source of the carbonatitic magmas from Amba Dongar containing recycled crustal components which base on nucleogenic neon compositions. Instead, the mantle source of both investigated carbonatite complexes is related to a primitive mantle plume source that we tentatively ascribe to the postulated Deccan mantle plume. If, as is commonly suggested, the present location of the Deccan mantle plume source is below Réunion Island, the currently observed more nucleogenic neon isotopic composition of the Réunion hotspot might be obliterated by significant upper mantle contributions. In addition, compared with other carbonatite complexes worldwide a rather significant contribution of atmospheric noble gases is observed. This is documented in cut-off 20Ne/22Ne-ratios of ca. 10.2 (Amba Dongar) and 10.45 (Siriwasan) and cut-off 40Ar/36Ar-ratios of about 1500. This atmospheric component had been added at shallow levels during the emplacement process or later during hydrothermal alteration. However, understanding the late-stage interaction between atmospheric gases and magmatic mantle fluids still requires further investigation.

Isotopic constraints on the genesis and evolution of basanitic lavas at Haleakala, Island of Maui, Hawaii

NASA Astrophysics Data System (ADS)

Phillips, Erin H.; Sims, Kenneth W. W.; Sherrod, David R.; Salters, Vincent J. M.; Blusztajn, Jurek; Dulai, Henrietta

2016-12-01

To understand the dynamics of solid mantle upwelling and melting in the Hawaiian plume, we present new major and trace element data, Nd, Sr, Hf, and Pb isotopic compositions, and 238U-230Th-226Ra and 235U-231Pa-227Ac activities for 13 Haleakala Crater nepheline normative basanites with ages ranging from ∼900 to 4100 yr B.P. These basanites of the Hana Volcanics exhibit an enrichment in incompatible trace elements and a more depleted isotopic signature than similarly aged Hawaiian shield lavas from Kilauea and Mauna Loa. Here we posit that as the Pacific lithosphere beneath the active shield volcanoes moves away from the center of the Hawaiian plume, increased incorporation of an intrinsic depleted component with relatively low 206Pb/204Pb produces the source of the basanites of the Hana Volcanics. Haleakala Crater basanites have average (230Th/238U) of 1.23 (n = 13), average age-corrected (226Ra/230Th) of 1.25 (n = 13), and average (231Pa/235U) of 1.67 (n = 4), significantly higher than Kilauea and Mauna Loa tholeiites. U-series modeling shows that solid mantle upwelling velocity for Haleakala Crater basanites ranges from ∼0.7 to 1.0 cm/yr, compared to ∼10 to 20 cm/yr for tholeiites and ∼1 to 2 cm/yr for alkali basalts. These modeling results indicate that solid mantle upwelling rates and porosity of the melting zone are lower for Hana Volcanics basanites than for shield-stage tholeiites from Kilauea and Mauna Loa and alkali basalts from Hualalai. The melting rate, which is directly proportional to both the solid mantle upwelling rate and the degree of melting, is therefore greatest in the center of the Hawaiian plume and lower on its periphery. Our results indicate that solid mantle upwelling velocity is at least 10 times higher at the center of the plume than at its periphery under Haleakala.

Volatile composition of microinclusions in diamonds from the Panda kimberlite, Canada: Implications for chemical and isotopic heterogeneity in the mantle

NASA Astrophysics Data System (ADS)

Burgess, Ray; Cartigny, Pierre; Harrison, Darrell; Hobson, Emily; Harris, Jeff

2009-03-01

In order to better investigate the compositions and the origins of fluids associated with diamond growth, we have carried-out combined noble gas (He and Ar), C and N isotope, K, Ca and halogen (Cl, Br, I) determinations on fragments of individual microinclusion-bearing diamonds from the Panda kimberlite, North West Territories, Canada. The fluid concentrations of halogens and noble gases in Panda diamonds are enriched by several orders of magnitude over typical upper mantle abundances. However, noble gas, C and N isotopic ratios ( 3He/ 4He = 4-6 Ra, 40Ar/ 36Ar = 20,000-30,000, δ 13C = -4.5‰ to -6.9‰ and δ 15N = -1.2‰ to -8.8‰) are within the worldwide range determined for fibrous diamonds and similar to the mid ocean ridge basalt (MORB) source value. The high 36Ar content of the diamonds (>1 × 10 -9 cm 3/g) is at least an order of magnitude higher than any previously reported mantle sample and enables the 36Ar content of the subcontinental lithospheric mantle to be estimated at ˜0.6 × 10 -12 cm 3/g, again similar to estimates for the MORB source. Three fluid types distinguished on the basis of Ca-K-Cl compositions are consistent with carbonatitic, silicic and saline end-members identified in previous studies of diamonds from worldwide sources. These fluid end-members also have distinct halogen ratios (Br/Cl and I/Cl). The role of subducted seawater-derived halogens, originally invoked to explain some of the halogen ratio variations in diamonds, is not considered an essential component in the formation of the fluids. In contrast, it is considered that large halogen fractionation of a primitive mantle ratio occurs during fluid-melt partitioning in forming silicic fluids, and during separation of an immiscible saline fluid.

Helium as a tracer for fluids released from Juan de Fuca lithosphere beneath the Cascadia forearc

USGS Publications Warehouse

McCrory, Patricia A.; Constantz, James E.; Hunt, Andrew G.; Blair, James Luke

2016-01-01

The ratio between helium isotopes (3He/4He) provides an excellent geochemical tracer for investigating the sources of fluids sampled at the Earth's surface. 3He/4He values observed in 25 mineral springs and wells above the Cascadia forearc document a significant component of mantle-derived helium above Juan de Fuca lithosphere, as well as variability in 3He enrichment across the forearc. Sample sites arcward of the forearc mantle corner (FMC) generally yield significantly higher ratios (1.2-4.0 RA) than those seaward of the corner (0.03-0.7 RA). The highest ratios in the Cascadia forearc coincide with slab depths (40-45 km) where metamorphic dehydration of young oceanic lithosphere is expected to release significant fluid and where tectonic tremor occurs, whereas little fluid is expected to be released from the slab depths (25-30 km) beneath sites seaward of the corner.Tremor (considered a marker for high fluid pressure) and high RA values in the forearc are spatially correlated. The Cascadia tremor band is centered on its FMC, and we tentatively postulate that hydrated forearc mantle beneath Cascadia deflects a significant portion of slab-derived fluids updip along the subduction interface, to vent in the vicinity of its corner. Furthermore, high RA values within the tremor band just arcward of the FMC, suggest that the innermost mantle wedge is relatively permeable.Conceptual models require: (1) a deep fluid source as a medium to transport primordial 3He; (2) conduits through the lithosphere which serve to speed fluid ascent to the surface before significant dilution from radiogenic 4He can occur; and (3) near lithostatic fluid pressure to keep conduits open. Our spatial correlation between high RA values and tectonic tremor provides independent evidence that tremor is associated with deep fluids, and it further suggests that high pore pressures associated with tremor may serve to keep fractures open for 3He migration through ductile upper mantle and lower crust.

Specific features of basalts from the western part of Andrew Bain Fault, Southwest Indian Ridge

NASA Astrophysics Data System (ADS)

Peyve, A. A.; Skolotnev, S. G.

2017-12-01

This paper reports original data on the composition of volcanic rocks in the western part of the Andrew Bain Fault of the South-West Indian Ridge obtained in the 23rd voyage of R/V Akademik Nikolai Strakhov. In accordance with high La/Th and low Nb/U ratios, the basalt compositions of stations S2317, S2318, and S2330 could result from melting of the DM-type source with HIMU traces. Meanwhile, the enriched samples of station S2326 correspond to a mantle source with a considerable contribution of recycled sediments (EM). Sample S2326/35, which is composed of a melt almost completely depleted in EM material, corresponds to the volcanic rocks of the Marion and Prince Edward islands. The obtained and available data on the SWIR segment from Bouvet Island to Andrew Bain Fault are indicative of small mantle heterogeneities in this region. Two possible variants of their origin are considered: either preservation of the enriched material fragments in the depleted mantle during the split of Gondwana or "contamination" of the mantle with plume material with the formation of vein irregularities before opening of the ocean in this region. In the latter case, the plume material could cover a huge area not constrained by the young plume magmatism regions on Bouvet, Marion, and Prince Edward islands.

Petro-tectonic Analysis of the Plagiogranite Intrusions in the Khor Fakkan Block of the Semail Ophiolites

NASA Astrophysics Data System (ADS)

Kokkalas, S.; Joun, H.; Tombros, S.

2017-12-01

Plagiogranite intrusions are common in the Khor Fakkan block of the Semail ophiolite, where the mantle sequence is predominant. Several models have been proposed for the source of these leucocratic intrusions, but their genesis is still under debate. The examined plagiogranites are characterized by 68 wt. % SiO2 and display volcanic-arc granite affinity. They have crystallize at temperatures that range from 550° to 720o C and pressures ranging from 5.0 to 6.5 Kbars. The parental plagiogranite melts, based on the relations of the δ18Omelt or δ18OH2O versus eSr suggest mixing of subducted crust with overlying upper mantle. The relatively wide range of the 87Rb/86Sr ratios, at almost constant 87Sr/86Sr, implies that partial melting and mixing was followed by fractional crystallization. The isotopic ages from the examined plagiogranites range between 94.9-98.5 Ma, predating the sole metamorphism. Based on our source contribution calculations, 96% of the igneous and 4% of sedimentary end-member components are involved in formation of plagiogranitic melts. The igneous end-member derived from partial melting of 3 % upper mantle and 97% recycled oceanic crust. We propose that the mafic melts were initially produced by the off-axis melting of recycled oceanic slab under a compressional regime a supra-subduction zone (SSZ) setting. The mafic melts were modified due to mixing with small amount of melts from the upper mantle by influx of slab-derived fluids. Then these melts underwent extended fractional crystallization with crystallization of An-enriched plagioclase and emplaced on the Moho level to form Dadnah plagiogranites in the Khor Fakkan block.

Osmium isotope and highly siderophile element systematics of the lunar crust

NASA Astrophysics Data System (ADS)

Day, James M. D.; Walker, Richard J.; James, Odette B.; Puchtel, Igor S.

2010-01-01

Coupled 187Os/ 188Os and highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, and Re) abundance data are reported for pristine lunar crustal rocks 60025, 62255, 65315 (ferroan anorthosites, FAN) and 76535, 78235, 77215 and a norite clast in 15455 (magnesian-suite rocks, MGS). Osmium isotopes permit more refined discrimination than previously possible of samples that have been contaminated by meteoritic additions and the new results show that some rocks, previously identified as pristine, contain meteorite-derived HSE. Low HSE abundances in FAN and MGS rocks are consistent with derivation from a strongly HSE-depleted lunar mantle. At the time of formation, the lunar floatation crust, represented by FAN, had 1.4 ± 0.3 pg g - 1 Os, 1.5 ± 0.6 pg g - 1 Ir, 6.8 ± 2.7 pg g - 1 Ru, 16 ± 15 pg g - 1 Pt, 33 ± 30 pg g - 1 Pd and 0.29 ± 0.10 pg g - 1 Re (˜ 0.00002 × CI) and Re/Os ratios that were modestly elevated ( 187Re/ 188Os = 0.6 to 1.7) relative to CI chondrites. MGS samples are, on average, characterised by more elevated HSE abundances (˜ 0.00007 × CI) compared with FAN. This either reflects contrasting mantle-source HSE characteristics of FAN and MGS rocks, or different mantle-crust HSE fractionation behaviour during production of these lithologies. Previous studies of lunar impact-melt rocks have identified possible elevated Ru and Pd in lunar crustal target rocks. The new results provide no supporting evidence for such enrichments. If maximum estimates for HSE in the lunar mantle are compared with FAN and MGS averages, crust-mantle concentration ratios ( D-values) must be ≤ 0.3. Such D-values are broadly similar to those estimated for partitioning between the terrestrial crust and upper mantle, with the notable exception of Re. Given the presumably completely different mode of origin for the primary lunar floatation crust and tertiary terrestrial continental crust, the potential similarities in crust-mantle HSE partitioning for the Earth and Moon are somewhat surprising. Low HSE abundances in the lunar crust, coupled with estimates of HSE concentrations in the lunar mantle implies there may be a 'missing component' of late-accreted materials (as much as 95%) to the Moon if the Earth/Moon mass-flux estimates are correct and terrestrial mantle HSE abundances were established by late accretion.

Osmium isotope and highly siderophile element systematics of the lunar crust

USGS Publications Warehouse

Day, J.M.D.; Walker, R.J.; James, O.B.; Puchtel, I.S.

2010-01-01

Coupled 187Os/188Os and highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, and Re) abundance data are reported for pristine lunar crustal rocks 60025, 62255, 65315 (ferroan anorthosites, FAN) and 76535, 78235, 77215 and a norite clast in 15455 (magnesian-suite rocks, MGS). Osmium isotopes permit more refined discrimination than previously possible of samples that have been contaminated by meteoritic additions and the new results show that some rocks, previously identified as pristine, contain meteorite-derived HSE. Low HSE abundances in FAN and MGS rocks are consistent with derivation from a strongly HSE-depleted lunar mantle. At the time of formation, the lunar floatation crust, represented by FAN, had 1.4 ?? 0.3 pg g- 1 Os, 1.5 ?? 0.6 pg g- 1 Ir, 6.8 ?? 2.7 pg g- 1 Ru, 16 ?? 15 pg g- 1 Pt, 33 ?? 30 pg g- 1 Pd and 0.29 ?? 0.10 pg g- 1 Re (??? 0.00002 ?? CI) and Re/Os ratios that were modestly elevated (187Re/188Os = 0.6 to 1.7) relative to CI chondrites. MGS samples are, on average, characterised by more elevated HSE abundances (??? 0.00007 ?? CI) compared with FAN. This either reflects contrasting mantle-source HSE characteristics of FAN and MGS rocks, or different mantle-crust HSE fractionation behaviour during production of these lithologies. Previous studies of lunar impact-melt rocks have identified possible elevated Ru and Pd in lunar crustal target rocks. The new results provide no supporting evidence for such enrichments. If maximum estimates for HSE in the lunar mantle are compared with FAN and MGS averages, crust-mantle concentration ratios (D-values) must be ??? 0.3. Such D-values are broadly similar to those estimated for partitioning between the terrestrial crust and upper mantle, with the notable exception of Re. Given the presumably completely different mode of origin for the primary lunar floatation crust and tertiary terrestrial continental crust, the potential similarities in crust-mantle HSE partitioning for the Earth and Moon are somewhat surprising. Low HSE abundances in the lunar crust, coupled with estimates of HSE concentrations in the lunar mantle implies there may be a 'missing component' of late-accreted materials (as much as 95%) to the Moon if the Earth/Moon mass-flux estimates are correct and terrestrial mantle HSE abundances were established by late accretion. ?? 2009 Elsevier B.V. All rights reserved.

Incipient boninitic arc crust built on denudated mantle: the Khantaishir ophiolite (western Mongolia)

NASA Astrophysics Data System (ADS)

Gianola, Omar; Schmidt, Max W.; Jagoutz, Oliver; Sambuu, Oyungerel

2017-12-01

The 570 Ma old Khantaishir ophiolite is built by up to 4 km harzburgitic mantle with abundant pyroxenites and dunites followed by 2 km of hornblende-gabbros and gabbronorites and by a 2.5 km thick volcanic unit composed of a dyke + sill complex capped by pillow lavas and some volcanoclastics. The volcanics are mainly basaltic andesites and andesites (or boninites) with an average of 58.2 ± 1.0 wt% SiO2, X Mg = 0.61 ± 0.03 ( X Mg = molar MgO/(MgO + FeOtot), TiO2 = 0.4 ± 0.1 wt% and CaO = 7.5 ± 0.6 wt% (errors as 2 σ). Normalized trace element patterns show positive anomalies for Pb and Sr, a negative Nb-anomaly, large ion lithophile elements (LILE) concentrations between N- and E-MORB and distinctly depleted HREE. These characteristics indicate that the Khantaishir volcanics were derived from a refractory mantle source modified by a moderate slab-component, similar to boninites erupted along the Izu-Bonin-Mariana subduction system and to the Troodos and Betts Cove ophiolites. Most strikingly and despite almost complete outcrops over 260 km2, there is no remnant of any pre-existing MORB crust, suggesting that the magmatic suite of this ophiolite formed on completely denudated mantle, most likely upon subduction initiation. The architecture of this 4-5 km thick early arc crust resembles oceanic crust formed at mid ocean ridges, but lacks a sheeted dyke complex; volcanic edifices are not observed. Nevertheless, low melting pressures combined with moderate H2O-contents resulted in high-Si primitive melts, in abundant hornblende-gabbros and in a fast enrichment in bulk SiO2. Fractional crystallization modeling starting from the observed primitive melts (56.6 wt% SiO2) suggests that 25 wt% pyroxene + plagioclase fractionation is sufficient to form the average Khantaishir volcanic crust. Most of the fractionation happened in the mantle, the observed pyroxenite lenses and layers in and at the top of the harzburgites account for the required cumulate volumes. Finally, the multiply documented occurrence of highly depleted boninites during subduction initiation suggests a causal relationship of subduction initiation and highly depleted mantle. Possibly, a discontinuity between dense fertile and buoyant depleted mantle contributes to the sinking of the future dense subducting plate, while the buoyant depleted mantle of the future overriding plate forms the infant mantle wedge.

Petrogenesis of basalts from the Archean Matachewan Dike Swarm Superior Province of Canada

NASA Technical Reports Server (NTRS)

Nelson, Dennis O.

1987-01-01

The Matachewan Dike swarm of eastern Ontario comprises Archean age basalts that were emplaced in the greenstone, granite-greenstone, and metasedimentary terrains of the Superior Province of Canada. The basalts are Fe-rich tholeiites, characterized by the near ubiquitos presence of large, compositionally uniform, calcic plagioclase. Major and trace element whole-rock compositions, along with microprobe analyses of constituent phases, from a group of dikes from the eastern portion of the province, were evaluated to constrain petrological processes that operated during the formation and evolution of the magmas. Three compositional groupings, were identified within the dikes. One group has compositional characteristics similar to modern abyssal tholeiites and is termed morb-type. A second group, enriched in incompatible elements and light-REE enriched, is referred to as the enriched group. The third more populated group has intermediate characteristics and is termed the main group. The observation of both morb-type and enriched compositions within a single dike strongly argues for the contemporaneous existence of magmas derived through different processes. Mixing calculations suggest that two possibilities exist. The least evolved basalts lie on a mixing line between the morb-type and enriched group, suggesting mixing of magmas derived from heterogeneous mantle. Mixing of magmas derived from a depleted mantle with heterogeneous Archean crust can duplicate certain aspects of the Matachewan dike composition array.

Constraints on the Parental Melts of Enriched Shergottites from Image Analysis and High Pressure Experiments

NASA Technical Reports Server (NTRS)

Collinet, M.; Medard, E.; Devouard, B.; Peslier, A.

2012-01-01

Martian basalts can be classified in at least two geochemically different families: enriched and depleted shergottites. Enriched shergottites are characterized by higher incompatible element concentrations and initial Sr-87/Sr-86 and lower initial Nd-143/Nd-144 and Hf-176/Hf-177 than depleted shergottites [e.g. 1, 2]. It is now generally admitted that shergottites result from the melting of at least two distinct mantle reservoirs [e.g. 2, 3]. Some of the olivine-phyric shergottites (either depleted or enriched), the most magnesian Martian basalts, could represent primitive melts, which are of considerable interest to constrain mantle sources. Two depleted olivine-phyric shergottites, Yamato (Y) 980459 and Northwest Africa (NWA) 5789, are in equilibrium with their most magnesian olivine (Fig. 1) and their bulk rock compositions are inferred to represent primitive melts [4, 5]. Larkman Nunatak (LAR) 06319 [3, 6, 7] and NWA 1068 [8], the most magnesian enriched basalts, have bulk Mg# that are too high to be in equilibrium with their olivine megacryst cores. Parental melt compositions have been estimated by subtracting the most magnesian olivine from the bulk rock composition, assuming that olivine megacrysts have partially accumulated [3, 9]. However, because this technique does not account for the actual petrography of these meteorites, we used image analysis to study these rocks history, reconstruct their parent magma and understand the nature of olivine megacrysts.

Carbonatite and silicate melt metasomatism of the mantle surrounding the Hawaiian plume: Evidence from volatiles, trace elements, and radiogenic isotopes in rejuvenated-stage lavas from Niihau, Hawaii

NASA Astrophysics Data System (ADS)

Dixon, Jacqueline; Clague, David A.; Cousens, Brian; Monsalve, Maria Luisa; Uhl, Jessika

2008-09-01

We present new volatile, trace element, and radiogenic isotopic compositions for rejuvenated-stage lavas erupted on Niihau and its submarine northwest flank. Niihau rejuvenated-stage Kiekie Basalt lavas are mildly alkalic and are isotopically similar to, though shifted to higher 87Sr/86Sr and lower 206Pb/204Pb than, rejuvenated-stage lavas erupted on other islands and marginal seafloor settings. Kiekie lavas display trace element heterogeneity greater than that of other rejuvenated-stage lavas, with enrichments in Ba, Sr, and light-rare earth elements resulting in high and highly variable Ba/Th and Sr/Ce. The high Ba/Th lavas are among the least silica-undersaturated of the rejuvenated-stage suite, implying that the greatest enrichments are associated with the largest extents of melting. Kiekie lavas also have high and variable H2O/Ce and Cl/La, up to 620 and 39, respectively. We model the trace element concentrations of most rejuvenated-stage lavas by small degrees (˜1% to 9%) of melting of depleted peridotite recently metasomatized by a few percent of an enriched incipient melt (0.5% melting) of the Hawaiian plume. Kiekie lavas are best explained by 4% to 13% partial melting of a peridotite source metasomatized by up to 0.2% carbonatite, similar in composition to oceanic carbonatites from the Canary and Cape Verde Islands, with lower proportion of incipient melt than that for other rejuvenated-stage lavas. Primary H2O and Cl of the carbonatite component must be high, but variability in the volatile data may be caused by heterogeneity in the carbonatite composition and/or interaction with seawater. Our model is consistent with predictions based on carbonated eclogite and peridotite melting experiments in which (1) carbonated eclogite and peridotite within the Hawaiian plume are the first to melt during plume ascent; (2) carbonatite melt metasomatizes plume and surrounding depleted peridotite; (3) as the plume rises, silica-undersaturated silicate melts are also produced and contribute to the metasomatic signature. The metasomatic component is best preserved at the margins of the plume, where low extents of melting of the metasomatized depleted mantle surrounding the plume are sampled during flexural uplift. Formation of carbonatite melts may provide a mechanism to transfer plume He to the margins of the plume.

Anomalous Alkali-Olivine Basalts Associated with Arc-related Late Cenozoic Volcanism in Southern Hispaniola

NASA Astrophysics Data System (ADS)

Lewis, J.; Perfit, M. R.; Kamenov, G.

2006-12-01

Several eruptive centers of Pliocene-Quaternary age occur across southern Hispaniola that constitutes the youngest land-based magmatic activity in the Greater Antilles. Two main rock suites can be delineated based on petrography, geochemistry and location. The older larger centers in the Dominican Republic (DR) consist of basalts (45.81-53% SiO2 with TiO2 <1.2%), basaltic andesites and trachybasalts (54-55% SiO2) and trachyandesites (56-62% SiO2). These constitute a consanguineous high-K calc-alkaline (CA) series. Younger centers of Quaternary age (all probably < 1.0 Ma) occur to the west in Haiti, at San Juan de la Maguana (DR) and two small centers to the south of Yayas de Viajama (DR). The rocks are alkali-olivine basalts, limburgites and nephelenites (38.6-47.6% SiO2 with TiO2 >1.7 at MgO<12%) and are termed the mafic alkaline (MA) series. Although there is an overall similarity in the trace and minor element patterns of normalized multi-element plots of the rocks samples the CA series shows distinct depletions in the HFS elements Ta, Nb, Hf, Zr, and Ti compared to lavas in the MA series. MA series samples exhibit strong enrichment in LREE (Ce/Ybn = > 30) compared to the CA series basalts (Ce/Ybn = < 30) and greater HREE depletions. The CA suite has higher 143Nd/144Nd (0.51286 ? 0.5126) and lower 87Sr/86Sr (0.7040 ? 0.7053) than the MA suite (0.5126-0.51196; 0.7063- 0.7078). MA series lavas have unusually non-radiogenic Pb isotopic values (206Pb/204Pb < 17.9) whereas the CA suite has low but values more typical of the Greater Antilles. Incompatible trace element ratios such as Ba/Nb, Sr/Nd, Ce/Yb and Ba/La are well correlated with isotopes but the data form near continuous arrays suggesting mixing between sources. The data suggest the young alkaline lavas are derived from enriched mantle source similar to EM1 but that they are also mixing with a component reflected in the composition of the CA series that is related to previous subduction- related enrichment of the sub-arc mantle beneath Hispaniola. The presence of an EM1 component in the Greater Antilles has not been previously recognized and is unusual for an arc environment.

Geochemical and isotopic constraints on island arc, synorogenic, post-orogenic and anorogenic granitoids in the Arabian Shield, Saudi Arabia

NASA Astrophysics Data System (ADS)

Robinson, F. A.; Foden, J. D.; Collins, A. S.

2015-04-01

The Arabian Shield preserves a protracted magmatic record of repeated amalgamation of juvenile subduction terranes that host granite intrusions ranging in age from the early Neoproterozoic to the Cambrian, which were emplaced into convergent and within-plate settings. Geochronology and whole-rock geochemistry of sampled Saudi Arabian granitoids define and distinguish four discrete age groups: 1) ~ 845-700 Ma island arc and synorogenic granitoids (IA + Syn), 2) ~ 640-610 Ma granitoids from the Nabitah and Halaban Suture (NHSG), 3) ~ 610-600 Ma post-orogenic perthitic (hypersolvus) granitoids (POPG), and 4) < 600 Ma anorogenic aegirine-bearing perthitic (hypersolvus) granitoids (AAPG). Groups 1, 2 and 3 include suites ranging from I-S- to A-type granites that have REE signatures typical of volcanic arc settings and show intra-suite variation that could be controlled by a combination of crustal assimilation and fractional crystallisation. Their mafic parental magmas have N-MORB-, or arc-tholeiite-like geochemistry. By contrast, group 4 A-type granites are more enriched in HREE and in incompatible elements such as Nb, Rb, Ga, Nd, Zr and Y and have lower Ce/Yb and higher Y/Nb ratios. These granitoids are interpreted to have been emplaced into within-plate and back-arc settings. Granitoid data also provide evidence that there may be two distinct mantle sources to the mafic parents of the granite suites. These are distinguished as contaminated and enriched mantle using Nb and Y and Nd isotopes. All granitoid suites are isotopically juvenile (ɛNd + 3 to + 6) and fall between the upper field crustal values of the Paleoproterozoic Khida terrane (ɛNd + 1) and contemporary depleted mantle. However, Nd isotopes distinguish contamination in group 1-3 mafic end-members beneath sutures which are interpreted to be derived from the contemporary MORB-type mantle wedge with subsequent crustal assimilation and fractionation to I- and A-type granitoids. The youngest (after 600 Ma) A-types (group 4) emplaced into extensional within-plate and back-arc settings require a new enriched mantle source that this study interprets to be associated with delamination.

Evolution of the upper mantle beneath the southern Baikal rift zone: an Sr-Nd isotope study of xenoliths from the Bartoy volcanoes

NASA Astrophysics Data System (ADS)

Ionov, D. A.; Kramm, U.; Stosch, H.-G.

1992-06-01

Anhydrous and amphibole-bearing peridotite xenoliths occur in roughly equal quantitites in the Bartoy volcanic field about 100 km south of the southern tip of Lake Baikal in Siberia (Russia). Whole-rock samples and pure mineral separates from nine xenoliths have been analyzed for Sr and Nd isotopes in order to characterize the upper mantle beneath the southern Baikal rift zone. In an Sr-Nd isotope diagram both dry and hydrous xenoliths from Bartoy plot at the junction between the fields of MORB and ocean island basalts. This contrasts with data available on two other localities around Lake Baikal (Tariat and Vitim) where peridotites typically have Sr-Nd isotope compositions indicative of strong long-term depletion in incompatible elements. Our data indicate significant chemical and isotopic heterogeneity in the mantle beneath Bartoy that may be attributed to its position close to an ancient suture zone separating the Siberian Platform from the Mongol-Okhotsk mobile belt and occupied now by the Baikal rift. Two peridotites have clinopyroxenes depleted in light rare earth elements (LREE) with Sr and Nd model ages of about 2 Ga and seem to retain the trace element and isotopic signatures of old depleted lithospheric mantle, while all other xenoliths show different degrees of LREE-enrichment. Amphiboles and clinopyroxenes in the hydrous peridotites are in Sr-Nd isotopic disequilibrium. If this reflects in situ decay of 147Sm and 87Rb rather than heterogeneities produced by recent metasomatic formation of amphiboles then 300 400 Ma have passed since the minerals were last in equilibrium. This age range then indicates an old enrichment episode or repeated events during the Paleozoic in the lithospheric mantle initially depleted maybe ˜2 Ga ago. The Bartoy hydrous and enriched dry peridotites, therefore, are unlikely to represent fragments of a young asthenospheric bulge which, according to seismic reflection studies, reached the Moho at the axis of the Baikal rift zone a few Ma ago. By contrast, hydrous veins in peridotites may be associated with rift formation processes.

Distribution of lithium in the Cordilleran Mantle wedge

NASA Astrophysics Data System (ADS)

Shervais, J. W.; Jean, M. M.; Seitz, H. M.

2015-12-01

Enriched fluid-mobile element (i.e., B, Li, Be) concentrations in peridotites from the Coast Range ophiolite are compelling evidence that this ophiolite originated in a subduction environment. A new method presented in Shervais and Jean (2012) for modeling the fluid enrichment process, represents the total addition of material to the mantle wedge source region and can be applied to any refractory mantle peridotite that has been modified by melt extraction and/or metasomatism. Although the end-result is attributed to an added flux of aqueous fluid or fluid-rich melt phase derived from the subducting slab, in the range of tens of parts per million - the nature and composition of this fluid could not be constrained. To address fluid(s) origins, we have analyzed Li isotopes in bulk rock peridotite and eclogite, and garnet separates, to identify possible sources, and fluid flow mechanisms and pathways. Bulk rock Li abundances of CRO peridotites (δ7Li = -14.3 to 5.5‰; 1.9-7.5 ppm) are indicative of Li addition and δ7Li-values are lighter than normal upper mantle values. However, Li abundances of clino- and orthopyroxene appear to record different processes operating during the CRO-mantle evolution. Low Li abundances in orthopyroxene (<1 ppm) suggest depletion via partial melting, whereas high concentrations in clinopyroxenes (>2 ppm) record subsequent interaction with Li-enriched fluids (or melts). The preferential partitioning of lithium in clinopyroxene could be indicative of a particular metasomatic agent, e.g., fluids from a dehydrating slab. Future in-situ peridotite isotope studies via laser ablation will further elucidate the fractionation of lithium between orthopyroxene, clinopyroxene, and serpentine. To obtain a more complete picture of the slab to arc transfer processes, we also measured eclogites and garnet separates to δ7Li= -18 to 3.5‰ (11.5-32.5 ppm) and δ7Li= 1.9 to 11.7‰ (0.7-3.9 ppm), respectively. In connection with previous studies focused on high-grade metamorphic assemblages within the Franciscan complex, an overall framework exists to reconstruct the Li architecture of the Middle Jurassic-Cordilleran subduction zone.

The Chlorine Isotope Composition of Earth’s Mantle

NASA Astrophysics Data System (ADS)

Bonifacie, M.; Jendrzejewski, N.; Agrinier, P.; Humler, E.; Coleman, M.; Javoy, M.

2008-03-01

Chlorine stable isotope compositions (δ37Cl) of 22 mid-ocean ridge basalts (MORBs) correlate with Cl content. The high-δ37Cl, Cl-rich basalts are highly contaminated by Cl-rich materials (seawater, brines, or altered rocks). The low-δ37Cl, Cl-poor basalts approach the composition of uncontaminated, mantle-derived magmas. Thus, most or all oceanic lavas are contaminated to some extent during their emplacement. MORB-source mantle has δ37Cl ≤ 1.6 per mil (‰), which is significantly lower than that of surface reservoirs (~ 0‰). This isotopic difference between the surface and deep Earth results from net Cl isotopic fractionation (associated with removal of Cl from the mantle and its return by subduction over Earth history) and/or the addition (to external reservoirs) of a late volatile supply that is 37Cl-enriched.

Mantle metasomatism above subduction zones: Trace-element and radiogenic isotope characteristics of peridotite xenoliths from Batan Island (Philippines)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Vidal, Ph.; Dupuy, C.; Maury, R.

1989-12-01

Trace-element abundances and radiogenic isotope ratios have been determined for a suite of upper mantle-derived xenoliths collected from Pliocene-Quaternary andesitic lavas on Batan Island, northernmost Philippines. The xenoliths exhibit mineralogical changes and large ion lithophile enrichment indicative of metasomatism involving H{sub 2}O-rich fluids. Strontium and neodymium isotopes in the xenoliths are not totally consistent with those in host lavas, but a common signature is indicated by the fact that all samples plot below the mantle array. The flux of fluids in the mantle wedge probably occurred over a long period of time. The flux induced large but variable changes inmore » mineral and trace and isotopic compositions, and ultimately resulted in the melting of the peridotites and production of island-arc lavas.« less

Effects of iron on the lattice thermal conductivity of Earth's deep mantle and implications for mantle dynamics

NASA Astrophysics Data System (ADS)

Hsieh, Wen-Pin; Deschamps, Frédéric; Okuchi, Takuo; Lin, Jung-Fu

2018-04-01

Iron may critically influence the physical properties and thermochemical structures of Earth's lower mantle. Its effects on thermal conductivity, with possible consequences on heat transfer and mantle dynamics, however, remain largely unknown. We measured the lattice thermal conductivity of lower-mantle ferropericlase to 120 GPa using the ultrafast optical pump-probe technique in a diamond anvil cell. The thermal conductivity of ferropericlase with 56% iron significantly drops by a factor of 1.8 across the spin transition around 53 GPa, while that with 8–10% iron increases monotonically with pressure, causing an enhanced iron substitution effect in the low-spin state. Combined with bridgmanite data, modeling of our results provides a self-consistent radial profile of lower-mantle thermal conductivity, which is dominated by pressure, temperature, and iron effects, and shows a twofold increase from top to bottom of the lower mantle. Such increase in thermal conductivity may delay the cooling of the core, while its decrease with iron content may enhance the dynamics of large low shear-wave velocity provinces. Our findings further show that, if hot and strongly enriched in iron, the seismic ultralow velocity zones have exceptionally low conductivity, thus delaying their cooling.

Effects of iron on the lattice thermal conductivity of Earth's deep mantle and implications for mantle dynamics.

PubMed

Hsieh, Wen-Pin; Deschamps, Frédéric; Okuchi, Takuo; Lin, Jung-Fu

2018-04-17

Iron may critically influence the physical properties and thermochemical structures of Earth's lower mantle. Its effects on thermal conductivity, with possible consequences on heat transfer and mantle dynamics, however, remain largely unknown. We measured the lattice thermal conductivity of lower-mantle ferropericlase to 120 GPa using the ultrafast optical pump-probe technique in a diamond anvil cell. The thermal conductivity of ferropericlase with 56% iron significantly drops by a factor of 1.8 across the spin transition around 53 GPa, while that with 8-10% iron increases monotonically with pressure, causing an enhanced iron substitution effect in the low-spin state. Combined with bridgmanite data, modeling of our results provides a self-consistent radial profile of lower-mantle thermal conductivity, which is dominated by pressure, temperature, and iron effects, and shows a twofold increase from top to bottom of the lower mantle. Such increase in thermal conductivity may delay the cooling of the core, while its decrease with iron content may enhance the dynamics of large low shear-wave velocity provinces. Our findings further show that, if hot and strongly enriched in iron, the seismic ultralow velocity zones have exceptionally low conductivity, thus delaying their cooling.

Evolved Rocks in Ocean Islands Formed by Melting of Metasomatized Mantle

NASA Astrophysics Data System (ADS)

Ashwal, L. D.; Torsvik, T. H.; Horvath, P.; Harris, C.; Webb, S. J.; Werner, S. C.; Corfu, F.

2015-12-01

Evolved rocks like trachyte occur as minor components of many plume-related basaltic ocean islands (e.g. Hawaii, Gran Canaria, Azores, Réunion), and are typically interpreted as products of extreme fractional crystallization from broadly basaltic magmas. Trachytes from Mauritius (Indian Ocean) suggest otherwise. Here, 6.8 Ma nepheline-bearing trachytes (SiO2 ~63%, Na2O + K2O ~12%) are enriched in all incompatible elements except Ba, Sr and Eu, which show prominent negative anomalies. Initial eNd values cluster at 4.03 ± 0.15 (n = 13), near the lower end of the range for Mauritian basalts (eNd = 3.70 - 5.75), but initial Sr is highly variable (ISr = 0.70408 - 0.71034) suggesting secondary deuteric alteration. Fractional crystallization models starting with a basaltic parent fail, because when plagioclase joins olivine in the crystallizing assemblage, residual liquids become depleted in Al2O3, produce no nepheline, and do not approach trachytic compositions. Mauritian basalts and trachytes do not fall near the ends of known miscibility gaps, eliminating liquid immiscibility processes. Partial melting of extant gabbroic bodies, either from the oceanic crust or from Réunion plume-related magmas should yield quartz-saturated melts different from the critically undersaturated Mauritian trachytes. A remaining possibility is that the trachytes represent direct, small-degree partial melts of fertile, perhaps metasomatized mantle. This is supported by the presence of trachytic glasses in many mantle xenoliths, and experimental results show that low-degree trachytic melts can be produced from mantle peridotites even under anhydrous conditions. If some feldspar is left behind as a residual phase, this would account for the negative Ba, Sr and Eu anomalies observed in Mauritian trachytes. Two trachyte samples that are less depleted in these elements contain xenocrysts of anorthoclase, Al-rich cpx and Cl-rich kaersutite that are out of equilibrium with host trachyte magmas; these may represent fragments of a refertilized mantle source. A model of direct, low-degree partial melting of metasomatized mantle may apply to other worldwide examples of evolved rocks in ocean islands.

An olivine-free mantle lithology as a source for mantle-derived magmas: the role of metasomes in the Ethiopian-Arabian large igneous province.

NASA Astrophysics Data System (ADS)

Rooney, T. O.; Nelson, W. R.; Ayalew, D.; Yirgu, G.; Herzberg, C. T.; Hanan, B. B.

2014-12-01

Peridotite constitutes most of the Earth's upper mantle, and it is therefore unsurprising that most mantle-derived magmas exhibit evidence of past equilibrium with olivine-dominated source. There is mounting evidence, however, for the role of pyroxenite in magma generation within upwelling mantle plumes; a less documented non-peridotite source of melts are metasomatic veins (metasomes) within the lithospheric mantle. Melts derived from metasomes may exhibit extreme enrichment or depletion in major and trace elements. We hypothesize that phenocrysts such as olivine, which are commonly used to probe basalt source lithology, will reflect these unusual geochemical signals. Here we present preliminary major and trace element analyses of 60 lavas erupted from a small Miocene shield volcano located within the Ethiopian flood basalt province. Erupted lavas are intercalated with lahars and pyroclastic horizons that are overlain by a later stage of activity manifested in small cinder cones and flows. The lavas form two distinctive petrographic and geochemical groups: (A) an olivine-phyric, low Ti group (1.7-2.7 wt. % TiO2; 4.0-13.6 wt. % MgO), which geochemically resembles most of the basalts in the region. These low Ti lavas are the only geochemical unit identified in the later cinder cones and associated lava flows. (B) a clinopyroxene-phyric high Ti group (1-6.7 wt. % TiO2; 1.0-9.5 wt. % MgO), which resembles the Oligocene HT-2 flood basalts. This unit is found intercalated with low Ti lavas within the Miocene shield. In comparison to the low Ti group, the high Ti lavas exhibit a profound depletion in Ni, Cr, Al, and Si, and significant enrichment in Ca, Fe, V, and the most incompatible trace elements. When combined with a diagnostic negative K anomaly in primitive-mantle normalized diagrams and Na2O>K2O, the geochemical data point towards a source which is rich in amphibole, devoid of olivine, and perhaps containing some carbonate. Our preliminary results have identified a large suite of primitive lavas derived from a nominally olivine-free mantle source. Consequently, our future work will examine olivine geochemical characteristics and constrain the compositional space for these unusual mantle lithologies.

The sources and time-integrated evolution of diamond-forming fluids - Trace elements and isotopic evidence

NASA Astrophysics Data System (ADS)

Klein-BenDavid, Ofra; Pearson, D. Graham; Nowell, Geoff M.; Ottley, Chris; McNeill, John C. R.; Logvinova, Alla; Sobolev, Nikolay V.

2014-01-01

Sub-micrometer inclusions in fibrous diamond growth zones carry high-density fluids (HDF) from which the host diamonds have precipitated. The chemistry of these fluids is our best opportunity of characterizing the diamond-forming environment. The major and trace element patterns of diamond-forming fluids vary widely. Such elemental signatures can be easily modified by a variety of mantle processes whereas radiogenic isotopes give a clear fingerprint of the time-integrated evolution of the fluid source region. Thus, the combination of elemental and isotope data is a powerful tool in constraining the origin of fluids from which diamonds precipitate. Here we present combined trace element composition (34 diamonds) and Sr isotopic data (23 diamonds) for fluid-rich diamonds from six worldwide locations. The Nd and Pb isotopic composition of two of the diamonds were also obtained. Several of the samples were analyzed in at least 2 locations to investigate variations in the fluid during diamond growth. The data was acquired using an off-line laser sampling technique followed by solution ICPMS and TIMS analysis. The Sr isotopic compositions of diamond fluids from the different suites range between convecting mantle values for Udachnaya (87Sr/86Sr363 = 0.70300 ± 16 to 0.70361 ± 4), to highly enriched values, up to 87Sr/86Sr = 0.72330 ± 3, for a diamond from Congo. No isochronous relationships were observed in any of the suites. The lowest Nd isotopic composition recorded so far in a diamond is from Congo (εNd71 = -40.4), which also contains the most radiogenic Sr isotopic composition. In contrast, a less enriched but still rather unradiogenic Nd isotope composition (εNd540 = -11) was obtained for a diamond from Snap Lake, which has moderately radiogenic Sr isotopic enrichment (87Sr/86Sr540 = 0.70821 ± 1). The Pb isotopic system measured in one diamond indicates a complex evolution for the fluid source, with extreme 207Pb/204Pb ratio (15.810 ± 3) and moderate, kimberlite-like 206Pb/204Pb and 208Pb/204Pb ratios. A multi-stage evolution of the diamond-forming fluids source can be constrained from our new isotopic data, indicating an Achaean enrichment event resulting in elevated U/Pb, Rb/Sr ratios and enrichment in LREEs. This source underwent a more recent fractionation, in the last 500 Myr that may have been related to the diamond-forming event. There is a strong correspondence between fluids with relatively unradiogenic Sr isotopes and relatively low (La, Nd, Sm)/(Nb, Zr) and (Ba, Th)/(Nb) ratios. Sr isotopic enrichment is accompanied by an increase in these ratios. The least trace element enriched and most isotopically depleted fluids are from the high-Mg carbonatitic suite. Thus, HDFs could be derived from asthenospheric mantle as low degree melts that interact to varying degrees with an ancient, metasomatized, rutile- and phlogopite bearing, sub continental lithosphere mantle. The internal heterogeneity in the Sr isotopic ratios within a single diamond suite and even within single diamonds may indicate fluid-mixing processes. Such mixing may occur during migration through preferred mantle veins and may be affected by the small-scale geochemical variability within them.

The variable role of slab-derived fluids in the generation of a suite of primitive calc-alkaline lavas from the Southernmost Cascades, California

USGS Publications Warehouse

Borg, L.E.; Clynne, M.A.; Bullen, T.D.

1997-01-01

The compositional continuum observed in primitive calc-alkaline lavas erupted from small volcanoes across the southernmost Cascade arc is produced by the introduction of a variable proportion of slab-derived fluid into the superjacent peridotite layer of the mantle wedge. Magmas derived from fluid-rich sources are erupted primarily in the forearc and are characterized by Sr and Pb enrichment (primitive mantle-normalized Sr/P > 5.5), depletions of Ta and Nb, low incompatible-element abundances, and MORB-like Sr and Pb isotopic ratios. Magmas derived from fluid-poor sources are erupted primarily in the arc axis and behind the arc, and are characterized by weak enrichment in Sr [1.0 < (Sr/P)N < 1.3], weak depletions in Ta and Nb, higher incompatible-element abundances, and OIB-like Sr, Nd, and Pb isotopic ratios. Fluxing the mantle wedge above the subducting slab with H2O-rich fluid stabilizes amphibole and enriches the wedge peridotites in incompatible elements, particularly unradiogenic Sr and Pb. The hydrated amphibole-bearing portion of the mantle wedge is downdragged beneath the forearc, where its solidus is exceeded, yielding melts that are enriched in Sr and Pb, and depleted in Ta and Nb (reflecting both high Sr and Pb relative to Ta and Nb in the fluid, and the greater compatibility of Ta and Nb in amphibole compared to other silicate phases in the wedge). A steady decrease of the fluid-contributed geochemical signature away from the trench is produced by the progressive dehydration of the downdragged portion of the mantle wedge with depth, resulting from melt extraction and increased temperature at the slab-wedge interface. Inverse correlation between incompatible-element abundances and the size of the fluid-contributed geochemical signature is generated by melting of more depleted peridotites, rather than by significant differences in the degree of melting. High-(Sr/P)N lavas of the forearc are generated by melting of a MORB-source-like peridotite that has been fluxed with a greater proportion of slab-derived fluid, and low (Sr/P)N lavas of the arc axis are produced by melting of an OIB-source-like peridotite in the presence of a smaller proportion of slab-derived fluid. This study documents the control that a slab-derived fluid can have on incompatible element and isotopic systematics of arc magmas by 1) the addition of incompatible elements to the wedge, 2) the stabilization of hydrous phases in the wedge, and 3) the lowering of peridotite solidi.

Lunar mare volcanism: Mixing of distinct, mantle source regions with KREEP-like component

NASA Technical Reports Server (NTRS)

Shervais, John W.; Vetter, Scott K.

1993-01-01

Mare basalts comprise less than 1% of the lunar crust, but they constitute our primary source of information on the moon's upper mantle. Compositional variations between mare basalt suites reflect variations in the mineralogical and geochemical composition of the lunar mantle which formed during early lunar differentiation (4.5-4.4 AE). Three broad suites of mare basalt are recognized: very low-Ti (VLT) basalts with TiO2 less than 1 wt%, low-Ti basalts with TiO2 = 2-4 wt%, and high-Ti basalts with TiO2 = 10-14 wt%. Important subgroups include the Apollo 12 ilmenite basalts (TiO2 = 5-6 wt%), aluminous low-Ti mare basalts (TiO2 = 2-4 wt%, Al2O3 = 10-14 wt%), and the newly discovered Very High potassium (VHK) aluminous low-Ti basalts, with K2O = 0.4-1.5 wt%. The mare basalt source region has geochemical characteristics complementary to the highlands crust and is generally thought to consist of mafic cumulates from the magma ocean which formed the felsic crust by feldspar flotation. The progressive enrichment of mare basalts in Fe/Mg, alkalis, and incompatible trace elements in the sequence VLT basalt yields low-Ti basalt yields high-Ti basalt is explained by the remelting of mafic cumulates formed at progressively shallower depths in the evolving magma ocean. This model is also consistent with the observed decrease in compatible element concentrations and the progressive increase in negative Eu anomalies.

Geochemistry of southern Pagan Island lavas, Mariana arc: The role of subduction zone processes

USGS Publications Warehouse

Marske, J.P.; Pietruszka, A.J.; Trusdell, F.A.; Garcia, M.O.

2011-01-01

New major and trace element abundances, and Pb, Sr, and Nd isotopic ratios of Quaternary lavas from two adjacent volcanoes (South Pagan and the Central Volcanic Region, or CVR) located on Pagan Island allow us to investigate the mantle source (i.e., slab components) and melting dynamics within the Mariana intra-oceanic arc. Geologic mapping reveals a pre-caldera (780-9.4ka) and post-caldera (<9.4ka) eruptive stage for South Pagan, whereas the eruptive history of the older CVR is poorly constrained. Crystal fractionation and magma mixing were important crustal processes for lavas from both volcanoes. Geochemical and isotopic variations indicate that South Pagan and CVR lavas, and lavas from the northern volcano on the island, Mt. Pagan, originated from compositionally distinct parental magmas due to variations in slab contributions (sediment and aqueous fluid) to the mantle wedge and the extent of mantle partial melting. A mixing model based on Pb and Nd isotopic ratios suggests that the average amount of sediment in the source of CVR (~2.1%) and South Pagan (~1.8%) lavas is slightly higher than Mt. Pagan (~1.4%) lavas. These estimates span the range of sediment-poor Guguan (~1.3%) and sediment-rich Agrigan (~2.0%) lavas for the Mariana arc. Melt modeling demonstrates that the saucer-shaped normalized rare earth element (REE) patterns observed in Pagan lavas can arise from partial melting of a mixed source of depleted mantle and enriched sediment, and do not require amphibole interaction or fractionation to depress the middle REE abundances of the lavas. The modeled degree of mantle partial melting for Agrigan (2-5%), Pagan (3-7%), and Guguan (9-15%) lavas correlates with indicators of fluid addition (e.g., Ba/Th). This relationship suggests that the fluid flux to the mantle wedge is the dominant control on the extent of partial melting beneath Mariana arc volcanoes. A decrease in the amount of fluid addition (lower Ba/Th) and extent of melting (higher Sm/Yb), and an increase in the sediment contribution (higher Th/Nb, La/Sm, and Pb isotopic ratios) from Mt. Pagan to South Pagan could reflect systematic cross-arc or irregular along-arc melting variations. These observations indicate that the length scale of compositional heterogeneity in the mantle wedge beneath Mariana arc volcanoes is small (~10km).

Composition dependence of spin transition in (Mg,Fe)SiO 3 bridgmanite

DOE PAGES

Dorfman, Susannah M.; Badro, James; Rueff, Jean -Pascal; ...

2015-10-01

Spin transitions in (Mg,Fe)SiO 3 bridgmanite have important implications for the chemistry and dynamics of Earth’s lower mantle, but have been complex to characterize in experiments. We examine the spin state of Fe in highly Fe-enriched bridgmanite synthesized from enstatites with measured compositions (Mg 0.61Fe 0.38Ca 0.01)SiO 3 and (Mg 0.25Fe 0.74Ca 0.01)SiO 3. Bridgmanite was synthesized at 78-88 GPa and 1800-2400 K and X-ray emission spectra were measured on decompression to 1 bar (both compositions) and compression to 126 GPa ((Mg 0.61Fe 0.38Ca 0.01)SiO 3 only) without additional laser heating. Observed spectra confirm that Fe in these bridgmanites ismore » dominantly high spin in the lower mantle. However, the total spin moment begins to decrease at ~50 GPa in the 74% FeSiO 3 composition. Lastly, these results support density functional theory predictions of a lower spin transition pressure in highly Fe-enriched bridgmanite and potentially explain the high solubility of FeSiO 3 in bridgmanite at pressures corresponding to Earth’s deep lower mantle.« less

An overview of the association between lamprophyric intrusions and rare-metal mineralization

NASA Astrophysics Data System (ADS)

Štemprok, Miroslav; Seifert, Thomas

2011-01-01

Granite-related rare metal districts in orogenic settings are occasionally associated with lamprophyre dikes. We recorded 63 occurrences of lamprophyres in bimodal dike suites of about 200 granite bodies related to rare metal deposits. Most lamprophyres occur in Paleozoic and Mesozoic metallogenic provinces in the northern hemisphere. Lamprophyres which are associated with rare metal deposits are calc-alkaline (kersantites, minettes, spessartites) or more rarely alkaline lamprophyres (camptonites, monchiquites) which occur in the roof zone of complex granitic bodies as pre-granitic, intra-granitic, intra-ore or post-ore dikes. Most lamprophyres are spatially associated with dominant felsic dikes and/or with mafic dikes represented by diorites or diabases. Diorites and lamprophyres occasionally exhibit transitional compositions from one to another. Lamprophyres share common geochemical characteristics of highly evolved granitoids such as enrichment in K and F, increased abundances of Li, Rb, and Cs and enrichment in some HFSE (e.g. Zr, U, Th, Mo, Sn, W). Lamprophyres in rare metal districts testify to accessibility of the upper crust to mantle products at the time of rare metal mineralization and possible influence of mantle melts or mantle-derived fluids in the differentiation of granitic melts in the lower crust.

Petrology of spinel lherzolite xenoliths from Youkou volcano, Adamawa Massif, Cameroon Volcanic Line: mineralogical and geochemical fingerprints of sub-rift mantle processes

NASA Astrophysics Data System (ADS)

Njombie, Merlin Patrick Wagsong; Temdjim, Robert; Foley, Stephen F.

2018-02-01

The basaltic maar of Youkou, situated in the Adamawa Volcanic Massif in the eastern branch of the continental segment of the Cameroon Volcanic Line, contains mantle-derived xenoliths of various types in pyroclastites. Spinel-bearing lherzolite xenoliths from the Youkou volcano generally exhibit protogranular textures with olivine (Fo89.4-90.5), enstatite (En89 - 91Fs8.7-9.8Wo0.82-1.13), clinopyroxene, spinel (Cr#Sp = 9.4-13.8), and in some cases amphibole (Mg# = 88.5-89.1). Mineral equilibration temperatures in the lherzolite xenoliths have been estimated from three-two pyroxene thermometers and range between 835 and 937 °C at pressures of 10-18 kbar, consistent with shallow mantle depths of around 32-58 km. Trends displayed by bulk-rock MgO correlate with Al2O3, indicating that the xenoliths are refractory mantle residues after partial melting. The degree of partial melting estimated from spinel compositions is less than 10%: evidences for much higher degrees of depletion are preserved in one sample, but overprinted by refertilization in others. Trace element compositions of the xenoliths are enriched in highly incompatible elements (LREE, Sr, Ba, and U), indicating that the spinel lherzolites underwent later cryptic metasomatic enrichment induced by plume-related hydrous silicate melts. The extreme fertility (Al2O3 = 6.07-6.56 wt% in clinopyroxene) and the low CaO/Al2O3 ratios in the spinel lherzolites suggest that they could not be a simple residue of partial melting of primitive mantle and must have experienced refertilization processes driven by the infiltration of carbonatite or carbonated silicate melts.

The controversy over plumes: Who is actually right?

NASA Astrophysics Data System (ADS)

Puchkov, V. N.

2009-01-01

The current state of the theory of mantle plumes and its relation to classic plate tectonics show that the “plume” line of geodynamic research is in a period of serious crisis. The number of publications criticizing this concept is steadily increasing. The initial suggestions of plumes’ advocates are disputed, and not without grounds. Questions have been raised as to whether all plumes are derived from the mantle-core interface; whether they all have a wide head and a narrow tail; whether they are always accompanied by uplifting of the Earth’s surface; and whether they can be reliably identified by geochemical signatures, e.g., by the helium-isotope ratio. Rather convincing evidence indicates that plumes cannot be regarded as a strictly fixed reference frame for moving lithospheric plates. More generally, the very existence of plumes has become the subject of debate. Alternative ideas contend that all plumes, or hot spots, are directly related to plate-tectonic mechanisms and appear as a result of shallow tectonic stress, subsequent decompression, and melting of the mantle enriched in basaltic material. Attempts have been made to explain the regular variation in age of volcanoes in ocean ridges by the crack propagation mechanism or by drift of melted segregations of enriched mantle in a nearly horizontal asthenospheric flow. In the author’s opinion, the crisis may be overcome by returning to the beginnings of the plume concept and by providing an adequate specification of plume attributes. Only mantle flows with sources situated below the asthenosphere should be referred to as plumes. These flows are not directly related to such plate-tectonic mechanisms as passive rifting and decompression melting in the upper asthenosphere and are marked by time-progressive volcanic chains; their subasthenospheric roots are detected in seismic tomographic images. Such plumes are mostly located at the margins of superswells, regions of attenuation of seismic waves at the mantle-core interface.

Transcriptional profiles of supragranular-enriched genes associate with corticocortical network architecture in the human brain

PubMed Central

Krienen, Fenna M.; Yeo, B. T. Thomas; Ge, Tian; Buckner, Randy L.; Sherwood, Chet C.

2016-01-01

The human brain is patterned with disproportionately large, distributed cerebral networks that connect multiple association zones in the frontal, temporal, and parietal lobes. The expansion of the cortical surface, along with the emergence of long-range connectivity networks, may be reflected in changes to the underlying molecular architecture. Using the Allen Institute’s human brain transcriptional atlas, we demonstrate that genes particularly enriched in supragranular layers of the human cerebral cortex relative to mouse distinguish major cortical classes. The topography of transcriptional expression reflects large-scale brain network organization consistent with estimates from functional connectivity MRI and anatomical tracing in nonhuman primates. Microarray expression data for genes preferentially expressed in human upper layers (II/III), but enriched only in lower layers (V/VI) of mouse, were cross-correlated to identify molecular profiles across the cerebral cortex of postmortem human brains (n = 6). Unimodal sensory and motor zones have similar molecular profiles, despite being distributed across the cortical mantle. Sensory/motor profiles were anticorrelated with paralimbic and certain distributed association network profiles. Tests of alternative gene sets did not consistently distinguish sensory and motor regions from paralimbic and association regions: (i) genes enriched in supragranular layers in both humans and mice, (ii) genes cortically enriched in humans relative to nonhuman primates, (iii) genes related to connectivity in rodents, (iv) genes associated with human and mouse connectivity, and (v) 1,454 gene sets curated from known gene ontologies. Molecular innovations of upper cortical layers may be an important component in the evolution of long-range corticocortical projections. PMID:26739559

Transcriptional profiles of supragranular-enriched genes associate with corticocortical network architecture in the human brain.

PubMed

Krienen, Fenna M; Yeo, B T Thomas; Ge, Tian; Buckner, Randy L; Sherwood, Chet C

2016-01-26

The human brain is patterned with disproportionately large, distributed cerebral networks that connect multiple association zones in the frontal, temporal, and parietal lobes. The expansion of the cortical surface, along with the emergence of long-range connectivity networks, may be reflected in changes to the underlying molecular architecture. Using the Allen Institute's human brain transcriptional atlas, we demonstrate that genes particularly enriched in supragranular layers of the human cerebral cortex relative to mouse distinguish major cortical classes. The topography of transcriptional expression reflects large-scale brain network organization consistent with estimates from functional connectivity MRI and anatomical tracing in nonhuman primates. Microarray expression data for genes preferentially expressed in human upper layers (II/III), but enriched only in lower layers (V/VI) of mouse, were cross-correlated to identify molecular profiles across the cerebral cortex of postmortem human brains (n = 6). Unimodal sensory and motor zones have similar molecular profiles, despite being distributed across the cortical mantle. Sensory/motor profiles were anticorrelated with paralimbic and certain distributed association network profiles. Tests of alternative gene sets did not consistently distinguish sensory and motor regions from paralimbic and association regions: (i) genes enriched in supragranular layers in both humans and mice, (ii) genes cortically enriched in humans relative to nonhuman primates, (iii) genes related to connectivity in rodents, (iv) genes associated with human and mouse connectivity, and (v) 1,454 gene sets curated from known gene ontologies. Molecular innovations of upper cortical layers may be an important component in the evolution of long-range corticocortical projections.

The geochemistry of primitive volcanic rocks of the Ankaratra volcanic complex, and source enrichment processes in the genesis of the Cenozoic magmatism in Madagascar

NASA Astrophysics Data System (ADS)

Melluso, L.; Cucciniello, C.; le Roex, A. P.; Morra, V.

2016-07-01

The Ankaratra volcanic complex in central Madagascar consists of lava flows, domes, scoria cones, tuff rings and maars of Cenozoic age that are scattered over 3800 km2. The mafic rocks include olivine-leucite-nephelinites, basanites, alkali basalts and hawaiites, and tholeiitic basalts. Primitive samples have high Mg# (>60), high Cr and Ni concentrations; their mantle-normalized patterns peak at Nb and Ba, have troughs at K, and smoothly decrease towards the least incompatible elements. The Ankaratra mafic rocks show small variation in Sr-Nd-Pb isotopic compositions (e.g., 87Sr/86Sr = 0.70377-0.70446, 143Nd/144Nd = 0.51273-0.51280, 206Pb/204Pb = 18.25-18.87). These isotopic values differ markedly from those of Cenozoic mafic lavas of northern Madagascar and the Comoro archipelago, typical Indian Ocean MORB and oceanic basalt end-members. The patterns of olivine nephelinitic magmas can be obtained through 3-10% partial melting of a mantle source that was enriched by a Ca-rich alkaline melt, and that contained garnet, carbonates and phlogopite. The patterns of tholeiitic basalts can be obtained after 10-12% partial melting of a source enriched with lower amounts of the same alkaline melt, in the spinel- (and possibly amphibole-) facies mantle, hence in volumes where carbonate is not a factor. The significant isotopic change from the northernmost volcanic rocks of Madagascar and those in the central part of the island implicates a distinct source heterogeneity, and ultimately assess the role of the continental lithospheric mantle as source region. The source of at least some volcanic rocks of the still active Comoro archipelago may have suffered the same time-integrated geochemical and isotopic evolution as that of the northern Madagascar volcanic rocks.

Partial melting and melt percolation in the mantle: The message from Fe isotopes

NASA Astrophysics Data System (ADS)

Weyer, Stefan; Ionov, Dmitri A.

2007-07-01

High precision Fe isotope measurements have been performed on various mantle peridotites (fertile lherzolites, harzburgites, metasomatised Fe-enriched peridotites) and volcanic rocks (mainly oceanic basalts) from different localities and tectonic settings. The peridotites yield an average δ 56Fe = 0.01‰ and are significantly lighter than the basalts (average δ 56Fe = 0.11‰). Furthermore, the peridotites display a negative correlation of δ 56Fe with Mg# indicating a link between δ 56Fe and degrees of melt extraction. Taken together, these findings imply that Fe isotopes fractionate during partial melting, with heavy isotopes preferentially entering the melt. The slope of depletion trends (δ 56Fe versus Mg#) of the peridotites was used to model Fe isotope fractionation during partial melting, resulting in αmantle-melt ≈ 1.0001-1.0003 or ln αmantle-melt ≈ 0.1-0.3‰. In contrast to most other peridotites investigated in this study, spinel lherzolites and harzburgites from three localities (Horoman, Kamchatka and Lherz) are virtually unaffected by metasomatism. These three sites display a particularly good correlation and define an isotope fractionation factor of ln αmantle-melt ≈ 0.3‰. This modelled value implies Fe isotope fractionation between residual mantle and mantle-derived melts corresponding to Δ56Fe mantle-basalt ≈ 0.2-0.3‰, i.e. significantly higher than the observed difference between averages for all the peridotites and the basalts in this study (corresponding to Δ56Fe mantle-basalt ≈ 0.1‰). Either disequilibrium melting increased the modelled αmantle-melt for these particular sites or the difference between average peridotite and basalt may be reduced by partial re-equilibration between the isotopically heavy basalts and the isotopically light depleted lithospheric mantle during melt ascent. The slope of the weaker δ 56Fe-Mg# trend defined by the combined set of all mantle peridotites from this study is more consistent with the generally observed difference between peridotites and basalts; this slope was used here to estimate the Fe isotope composition of the fertile upper mantle (at Mg# = 0.894, δ 56Fe ≈ 0.02 ± 0.03‰). Besides partial melting, the Fe isotope composition of mantle peridotites can also be significantly modified by metasomatic events, e.g. melt percolation. At two localities (Tok, Siberia and Tariat, Mongolia) δ 56Fe correlates with iron contents of the peridotites, which was increased from about 8% to up to 14.5% FeO by post-melting melt percolation. This process produced a range of Fe isotope compositions in the percolation columns, from extremely light (δ 56Fe = - 0.42‰) to heavy (δ 56Fe = + 0.17‰). We propose reaction with isotopically heavy melts and diffusion (enrichment of light Fe isotopes) as the most likely processes that produced the large isotope variations at these sites. Thus, Fe isotopes might be used as a sensitive tracer to identify such metasomatic processes in the mantle.

Constraints on the Amount of deeply subducted Water from numerical Models in comparison with natural Samples

NASA Astrophysics Data System (ADS)

Konrad-Schmolke, M.; Halama, R.

2014-12-01

The subduction of hydrated slab mantle to beyond-arc depths is the most important and yet weakly constrained factor in the quantification of the Earth's deep geologic water cycle. During subduction of hydrated oceanic lithosphere, dehydration reactions in the downgoing plate lead to a partitioning of water between upper and lower plate. Water retained in the slab is recycled into the mantle where it controls its rheology and thus plate tectonic velocities. Hence, quantification of the water partitioning in subduction zones is crucial for the understanding of mass transfer between the Earth's surface and the mantle. Combined thermomechanical and thermodynamic models yield quantitative constraints on the water cycle in subduction zones, but unless model results can be linked to natural observations, the reliability of such models remains speculative. We present combined thermomechanical, thermodynamic and geochemical models of active and paleo-subduction zones, whose results can be tested with independent geochemical features in natural rocks. In active subduction zones, evidence for the validity of our model comes from the agreement between modeled and observed across-arc trends of boron concentrations and isotopic compositions in arc volcanic rocks. In the Kamchatkan subduction zone, for example, the model successfully predicts complex geochemical patterns and the spatial distribution of arc volcanoes. In paleo-subduction zones (e.g. Western Gneiss Region and Western Alps), constraints on the water budget and dehydration behavior of the subducting slab come from trace element zoning patterns in ultra-high pressure (UHP) garnets. Distinct enrichments of Cr, Ni and REE in the UHP zones of the garnets can be reconciled by our models that predict intense rehydration and trace element re-enrichment of the eclogites at UHP conditions by fluids released from the underlying slab mantle. Models of present-day subduction zones indicate the presence of 2.5-6 wt.% of water within the uppermost 15 km of the subducted slab mantle. Depending on hydration depth, between 25 and 90% of this water is recycled into the deeper mantle. The Lower Devonian example from the Western Gneiss Region indicates that subduction of water into the Earth's deeper mantle is an active process at least since the middle Paleozoic.

Petrogenesis of Neogene basaltic volcanism associated with the Lut block, eastern Iran: Implication for tectonic and metallogenic evolution

NASA Astrophysics Data System (ADS)

Saadat, Saeed

This dissertation presents petrochemical data concerning Neogene olivine basalts erupted both along the margins and within the micro-continental Lut block, eastern Iran, which is a part of the active Alpine-Himalayan orogenic belt. These data demonstrate the following: (1) Basalts that erupted from small monogenetic parasitic cones around the Bazman stratovolcano, Makran arc area, in the southern Lut block, are low-Ti sub-alkaline olivine basalts. Enrichments of LILE relative to LREE, and depletions in Nb and Ta relatively to LILE, are similar to those observed for other convergent plate boundary arc magmas around the world and suggest that these basalts formed by melting of subcontinental mantle modified by dehydration of the subducted Oman Sea oceanic lithosphere. (2) Northeast of Iran, an isolated outcrop of Neogene/Quaternary alkali olivine basalt, containing mantle and crustal xenoliths, formed by mixing of small melt fractions from both garnet and spinel-facies mantle. These melts rose to the surface along localized pathways associated with extension at the junction between the N-S right-lateral strike-slip faults and E-W left-lateral strike slip faults. The spinel-peridotite mantle xenoliths contained in the basalts, which equilibrated in the subcontinental lithosphere at depths of 30 to 60 km and temperatures of 965°C to 1065°C, do not preserve evidence of extensive metasomatic enrichment as has been inferred for the mantle below the Damavand volcano further to the west in north-central Iran. (3) Neogene mafic rocks within the central Lut block represent the last manifestation of a much more extensive mid-Tertiary magmatic event. These basalts formed from both OIB-like asthenosphere and subcontinental lithosphere which preserved chemical characteristics inherited from mid-Tertiary subduction associated with the collision of the Arabian with the Eurasian plate and closing of the Neotethys Ocean. Neogene/Quternary alkali olivine basalts erupted mainly along the major faults that bound the Lut block on the east and west. These low-volumes, low-degree melts have been formed by low variable degrees of partial melting of mantle source produced by upwelling asthenosphere replaced the thinned lithospheric mantle.

Investigating melting induced mantle heterogeneities in plate driven mantle convection models

NASA Astrophysics Data System (ADS)

Price, M.; Davies, H.; Panton, J.

2017-12-01

Observations from geochemistry and seismology continue to suggest a range of complex heterogeneity in Earth's mantle. In the deep mantle, two large low velocity provinces (LLVPs) have been regularly observed in seismic studies, with their longevity, composition and density compared to the surrounding mantle debated. The cause of these observed LLVPs is equally uncertain, with previous studies advocating either thermal or thermo-chemical causes. There is also evidence that these structures could provide chemically distinct reservoirs within the mantle, with recent studies also suggesting there may be additional reservoirs in the mantle, such as bridgmanite-enriched ancient mantle structures (BEAMS). One way to test these hypotheses is using computational models of the mantle, with models that capture the full 3D system being both complex and computationally expensive. Here we present results from our global mantle model TERRA. Using our model, we can track compositional variations in the convecting mantle that are generated by self-consistent, evolving melting zones. Alongside the melting, we track trace elements and other volatiles which can be partitioned during melting events, and expelled and recycled at the surface. Utilising plate reconstruction models as a boundary condition, the models generate the tectonic features observed at Earth's surface, while also organising the lower mantle into recognisable degree-two structures. This results in our models generating basaltic `oceanic' crusts which are then brought into the mantle at tectonic boundaries, providing additional chemical heterogeneity in the mantle volume. Finally, by utilising thermodynamic lookup tables to convert the final outputs from the model to seismic structures, together with resolution filters for global tomography models, we are able to make direct comparisons between our results and observations. By varying the parameters of the model, we investigate a range of current hypotheses for heterogeneity in the mantle. Our work attempts to reconcile the many proposed current ideas for the deep mantle, giving additional insight from modelling on the latest observations from other Deep Earth disciplines.

Experimental determination of C, F, and H partitioning between mantle minerals and carbonated basalt, CO2/Ba and CO2/Nb systematics of partial melting, and the CO2 contents of basaltic source regions

NASA Astrophysics Data System (ADS)

Rosenthal, A.; Hauri, E. H.; Hirschmann, M. M.

2015-02-01

To determine partitioning of C between upper mantle silicate minerals and basaltic melts, we executed 26 experiments between 0.8 and 3 GPa and 1250-1500 °C which yielded 37 mineral/glass pairs suitable for C analysis by secondary ion mass spectrometry (SIMS). To enhance detection limits, experiments were conducted with 13C-enriched bulk compositions. Independent measurements of 13C and 12C in coexisting phases produced two C partition coefficients for each mineral pair and allowed assessment of the approach to equilibrium during each experiment. Concentrations of C in olivine (ol), orthopyroxene (opx), clinopyroxene (cpx) and garnet (gt) range from 0.2 to 3.5 ppm, and resulting C partition coefficients for ol/melt, opx/melt, cpx/melt and gt/melt are, respectively, 0.0007 ± 0.0004 (n = 2), 0.0003 ± 0.0002 (n = 45), 0.0005 ± 0.0004 (n = 17) and 0.0001 ± 0.00007 (n = 5). The effective partition coefficient of C during partial melting of peridotite is 0.00055 ± 0.00025, and therefore C is significantly more incompatible than Nb, slightly more compatible than Ba, and, among refractory trace elements, most similar in behavior to U or Th. Experiments also yielded partition coefficients for F and H between minerals and melts. Combining new and previous values of DFmineral/melt yields bulk DFperidotite/melt = 0.011 ± 0.002, which suggests that F behaves similarly to La during partial melting of peridotite. Values of DHpyx/melt correlate with tetrahedral Al along a trend consistent with previously published determinations. Small-degree partial melting of the mantle results in considerable CO2/Nb fractionation, which is likely the cause of high CO2/Nb evident in some Nb-rich oceanic basalts. CO2/Ba is much less easily fractionated, with incompatible-element-enriched partial melts having lower CO2/Ba than less enriched basalts. Comparison of calculated behavior of CO2, Nb, and Ba to systematics of oceanic basalts suggests that depleted (DMM-like) sources have 75 ± 25 ppm CO2 (CO2/Nb = 505 ± 168, CO2/Ba = 133 ± 44), whereas enriched sources of intraplate basalts similar in concentrations to primitive mantle have 600 ± 200 ppm CO2. If all mantle reservoirs are expressed in the current inventory of oceanic basalts for which nearly undegassed CO2 concentrations are available, then we estimate the likely range of mantle C concentrations to be 1.4-4.8 × 1023 grams of C, or 1.5-5.2 times the mass of the current C surface reservoir. Depending on the assumed Ba and Nb contents of average oceanic crust, resulting ridge fluxes of C range from 7.2 × 1013 to 2.9 × 1014 g/yr.

The boron and lithium isotopic composition of mid-ocean ridge basalts and the mantle

NASA Astrophysics Data System (ADS)

Marschall, Horst R.; Wanless, V. Dorsey; Shimizu, Nobumichi; Pogge von Strandmann, Philip A. E.; Elliott, Tim; Monteleone, Brian D.

2017-06-01

A global selection of 56 mid-ocean ridge basalt (MORB) glasses were analysed for Li and B abundances and isotopic compositions. Analytical accuracy and precision of analyses constitute an improvement over previously published MORB data and allow a more detailed discussion of the Li and B systematics of the crust-mantle system. Refined estimates for primitive mantle abundances ([ Li ] = 1.39 ± 0.10 μg/g and [ B ] = 0.19 ± 0.02 μg/g) and depleted mantle abundances ([ Li ] = 1.20 ± 0.10 μg/g and [ B ] = 0.077 ± 0.010 μg/g) are presented based on mass balance and on partial melting models that utilise observed element ratios in MORB. Assimilation of seawater (or brine) or seawater-altered material beneath the ridge, identified by high Cl / K , causes significant elevation of MORB δ11 B and variable elevation in δ7 Li . The B isotope ratio is, hence, identified as a reliable indicator of assimilation in MORB and values higher than -6‰ are strongly indicative of shallow contamination of the magma. The global set of samples investigated here were produced at various degrees of partial melting and include depleted and enriched MORB from slow and fast-spreading ridge segments with a range of radiogenic isotope signatures and trace element compositions. Uncontaminated (low- Cl / K) MORB show no significant boron isotope variation at the current level of analytical precision, and hence a homogenous B isotopic composition of δ11 B = - 7.1 ± 0.9 ‰ (mean of six ridge segments; 2SD). Boron isotope fractionation during mantle melting and basalt fractionation likely is small, and this δ11 B value reflects the B isotopic composition of the depleted mantle and the bulk silicate Earth, probably within ±0.4‰. Our sample set shows a mean δ7 Li = + 3.5 ± 1.0 ‰ (mean of five ridge segments; 2SD), excluding high- Cl / K samples. A significant variation of 1.0-1.5‰ exists among various ridge segments and among samples within individual ridge segments, but this variation is unrelated to differentiation, assimilation or mantle source indicators, such as radiogenic isotopes or trace elements. It, therefore, seems likely that kinetic fractionation of Li isotopes during magma extraction, transport and storage may generate δ7 Li excursions in MORB. No mantle heterogeneities, such as those generated by deeply recycled subducted materials, are invoked in the interpretation of the Li and B isotope data presented here, in contrast to previous work on smaller data sets. Lithium and boron budgets for the silicate Earth are presented that are based on isotope and element mass balance. A refined estimate for the B isotopic composition of the bulk continental crust is given as δ11 B = - 9.1 ± 2.4 ‰ . Mass balance allows the existence of recycled B reservoirs in the deep mantle, but these are not required. However, mass balance among the crust, sediments and seawater shows enrichment of 6 Li in the surface reservoirs, which requires the existence of 7 Li -enriched material in the mantle. This may have formed by the subduction of altered oceanic crust since the Archaean.

Melt/mantle interaction and melt evolution in the Sartohay high-Al chromite deposits of the Dalabute ophiolite (NW China)

NASA Astrophysics Data System (ADS)

Zhou, M.-F.; Robinson, P. T.; Malpas, J.; Aitchison, J.; Sun, M.; Bai, W.-J.; Hu, X.-F.; Yang, J.-S.

2001-06-01

The Sartohay block of the Dalabute ophiolite consists chiefly of mantle harzburgite and lherzolite with minor dunite. These rocks host voluminous chromite deposits with lenticular or vein-like shapes. The podiform chromitites are associated with, and cross-cut by, numerous troctolite dykes. Chromite in the chromitites has Al 2O 3 (23-31 wt%), TiO 2 (0.29-0.44 wt%), and Cr 2O 3 contents (<45 wt%) with Cr#s [100Cr/(Cr+Al)] (<60), typical of high-Al chromite deposits. The host peridotites in Sartohay have been texturally and geochemically modified by magmas from which the high-Al chromitites and mafic dykes formed. Dunites commonly envelop the podiform chromite bodies and show transitional contacts with the peridotites. Some of the peridotites and chromitites contain plagioclase that crystallized from impregnated melts. The dunite locally grades into troctolite with increasing plagioclase contents. As a result of melt impregnation, peridotites and dunites show variable Ca and Al contents and LREE enrichment. The parental magma of the chromitites was likely tholeiitic in composition, derived from partial melting of the asthenospheric mantle in a rising diapir. The interaction between this magma and pre-existing lithospheric mantle, composed of depleted lherzolite, would have formed a more silicic, tholeiitic magma from which high-Al chromitites crystallized. During this interaction, harzburgite and dunite were depleted in modal pyroxene and enriched in some incompatible elements (such as Al, Ca and LREE) due to melt impregnation.

Petrogenesis and tectonic implications of gabbro and plagiogranite intrusions in mantle peridotites of the Myitkyina ophiolite, Myanmar

NASA Astrophysics Data System (ADS)

Xu, Yang; Liu, Chuan-Zhou; Chen, Yi; Guo, Shun; Wang, Jian-Gang; Sein, Kyaing

2017-07-01

Centimeter-size intrusions of gabbros and plagiogranites occur in mantle peridotites of the Myitkyina ophiolite, Myanmar. The gabbros mainly consist of plagioclase and clinopyroxene, whereas orthopyroxene occasionally occurs. The plagiogranites are mainly composed of plagioclase, quartz and amphibole, with small amount of accessory minerals, such as zircon, apatite and rutile. Plagioclase in the gabbros varies from andesine to anorthite (An37-91), whereas plagioclase in the plagiogranites is less calcic (An1-40). Clinopyroxene in the gabbros is pervasively altered to hornblende. The gabbros contain 42.97-52.88 wt% SiO2, which show negative correlations with Al2O3, CaO and MgO, but positive correlations with Na2O, P2O5 and TiO2. Microtextural relations reveal the crystallization of clinopyroxene prior to plagioclase in the Myitkyina gabbros. This suggests that the gabbros were crystallized from hydrous melts, which is also supported by the occurrence of orthopyroxene and anorthitic plagioclase in some gabbros. The gabbros have slightly enriched Sr-Nd isotopes, with initial 87Sr/86Sr ratios of 0.703938-0.706609 and εNd(t) values of + 2.4-+7.2, and relatively variable Hf isotopes, with εHf(t) values of + 13.4-+24.9. A subduction component is required to explain the decoupled Nd-Hf isotopes of the gabbros. Binary mixing suggests that addition of ca 2% subducted sediments to a depleted mantle can account for the Nd-Hf decoupling. Therefore, both petrological and geochemical data of the gabbros support that the Myitkyina ophiolite was originated in a supra-subduction zone setting. The plagiogranites have compositions of tonalites and trondhjemites, containing 56.93-77.93 wt% SiO2, 1.27-10.79 wt% Na2O and 0.05-0.71 wt% K2O. They are slightly enriched in LREE over HREE and display positive anomalies in Eu, Zr, Hf but negative Nb anomalies. Very low TiO2 contents (0.03-0.2 wt%) of the plagiogranites suggest that they were not products of fractional crystallization of MORB but were generated by hydrous melting of gabbros. This process is also supported by the nearly constant contents of both La and Yb with increasing SiO2 of the plagiogranites. The Sr-Nd-Hf isotopes of the plagiogranites indicate the involvement of crustal component in their genesis. We proposed that the Myitkyina plagiogranites were generated by partial melting of the mafic protoliths in the subducted slab.

Europium and strontium anomalies in the MORB source mantle

NASA Astrophysics Data System (ADS)

Tang, Ming; McDonough, William F.; Ash, Richard D.

2017-01-01

Lower crustal recycling depletes the continental crust of Eu and Sr and returns Eu and Sr enriched materials into the mantle (e.g., Tang et al., 2015, Geology). To test the hypothesis that the MORB source mantle balances the Eu and Sr deficits in the continental crust, we carried out high precision Eu/Eu∗ and Sr/Sr∗ measurement for 72 MORB glasses with MgO >8.5% from the Pacific, Indian, and Atlantic mid-ocean ridges. MORB glasses with MgO ⩾ 9 wt.% have a mean Eu/Eu∗ of 1.025 ± 0.025 (2 σm, n = 46) and Sr/Sr∗ of 1.242 ± 0.093 (2 σm, n = 41) and these ratios are positively correlated. These samples show both positive and negative Eu and Sr anomalies, with no correlations between Eu/Eu∗ vs. MgO or Sr/Sr∗ vs. MgO, suggesting that the anomalies are not produced by plagioclase fractionation at MgO >9 wt.% and, thus, other processes must be responsible for generating the anomalies. We term these MORB samples primitive MORBs, as they record the melt Eu/Eu∗ and Sr/Sr∗ before plagioclase fractionation. Consequently, the mean oceanic crust, including cumulates, has a bulk Eu/Eu∗ of ∼1 and 20% Sr excess. Considering that divalent Sr and Eu(II) diffuse faster than trivalent Pr, Nd, Sm, and Gd, we evaluated this kinetic effect on Sm-Eu-Gd and Pr-Sr-Nd fractionations during spinel peridotite partial melting in the MORB source mantle. Our modeling shows that the correlated Eu and Sr anomalies seen in primitive MORBs may result from disequilibrium mantle melting. Melt fractions produced during early- and late-stage melting may carry positive and negative Eu and Sr anomalies, respectively, that overlap with the ranges documented in primitive MORBs. Because the net effect of disequilibrium melting is to produce partial melts with bulk positive Eu and Sr anomalies, the MORB source mantle must have Eu/Eu∗ < 1.025 ± 0.025 (2 σm) and Sr/Sr∗ < 1.242 ± 0.093 (2 σm). Although we cannot rule out the possibility that recycled lower continental crustal materials, which have positive Eu and Sr anomalies, are partially mixed into the upper mantle (i.e., MORB source region), a significant amount of this crustal component must have been sequestered into the deep mantle, as supported by the negative 206Pb/204Pb-Eu/Eu∗ and 206Pb/204Pb-Sr/Sr∗ correlations in ocean island basalts.

Topography: dusting for the fingerprints of mantle dynamics

NASA Astrophysics Data System (ADS)

Faccenna, C.; Becker, T. W.

2016-12-01

The surface of the Earth is an ever-changing expression of the dynamic processes occurring deep in the mantle and at and above its surface, but our ability to "read" landscapes in terms of their underlying tectonic or climatic forcing is rudimentary. During the last decade, particular attention has been drawn to the deep, convection-related component of topography, induced by the stress produced at the base of the lithosphere by mantle flow, and its relevance compared to the (iso)static component. Despite much progress, several issues, including the magnitude and rate of this dynamic component, remain open. Here, we use key sites from convergent margins (e.g., the Apennines) and from intraplate settings (e.g., Ethiopia) to estimate the amplitude and rate of topography change and to disentangle the dynamic from the static component. On the base of those and other examples, we introduce the concept of a Topographic Fingerprint: any combination of mantle, crustal and surface processes that will result in a distinctive, thus predictable, topographic expression.

Production and recycling of oceanic crust in the early Earth

NASA Astrophysics Data System (ADS)

van Thienen, P.; van den Berg, A. P.; Vlaar, N. J.

2004-08-01

Because of the strongly different conditions in the mantle of the early Earth regarding temperature and viscosity, present-day geodynamics cannot simply be extrapolated back to the early history of the Earth. We use numerical thermochemical convection models including partial melting and a simple mechanism for melt segregation and oceanic crust production to investigate an alternative suite of dynamics which may have been in operation in the early Earth. Our modelling results show three processes that may have played an important role in the production and recycling of oceanic crust: (1) Small-scale ( x×100 km) convection involving the lower crust and shallow upper mantle. Partial melting and thus crustal production takes place in the upwelling limb and delamination of the eclogitic lower crust in the downwelling limb. (2) Large-scale resurfacing events in which (nearly) the complete crust sinks into the (eventually lower) mantle, thereby forming a stable reservoir enriched in incompatible elements in the deep mantle. New crust is simultaneously formed at the surface from segregating melt. (3) Intrusion of lower mantle diapirs with a high excess temperature (about 250 K) into the upper mantle, causing massive melting and crustal growth. This allows for plumes in the Archean upper mantle with a much higher excess temperature than previously expected from theoretical considerations.

Petrology, geochemistry and Resbnd Os isotopes of peridotite xenoliths from Maguan, Yunnan Province: Implications for the Cenozoic mantle replacement in southwestern China

NASA Astrophysics Data System (ADS)

Liu, Chuan-Zhou; Wu, Fu-Yuan; Sun, Jing; Chu, Zhu-Yin; Yu, Xue-Hui

2013-05-01

Petrology, geochemistry and Resbnd Os isotopes of peridotite xenoliths from Maguan (Yunnan Province) are reported in this paper with the aims of constraining the age and evolution of the lithospheric mantle beneath the western margin of the Cathyasia block. The Maguan mantle xenoliths contain predominantly fertile lherzolites with whole-rock Al2O3 contents of 2.42-4.99 wt.%, and subordinate clinopyroxene-poor lherzolites with Al2O3 contents of 1.19-1.98 wt.%. Their whole-rock CaO, Al2O3 and Na2O decrease along with the increase of MgO, following melt depletion trends. This suggests that the Maguan lherzolites represent mantle residues after variable degrees of partial melting. Clinopyroxenes in the fertile lherzolites display flat to depleted REE patterns, whereas those in the clinopyroxene-poor lherzolites are variably enriched in LREE. Modeling results of Y and Yb contents in clinopyroxenes suggest that the fertile lherzolites have experienced ~ 1-5% degrees of partial melting, in contrast with ~ 10-15% for the clinopyroxene-poor lherzolites. Both fertile and clinopyroxene-poor lherzolites have similarly high equilibrium temperatures, i.e., 911-1120 °C versus 919-941 °C, respectively. The whole-rock 187Os/188Os ratios of clinopyroxene-poor lherzolites vary from 0.11764 to 0.12506, which are slightly lower than most fertile lherzolites (0.12272-0.12854). Their 187Os/188Os ratios show no correlation with 187Re/188Os ratios or bulk-rock Al2O3 contents. The rhenium depletion ages (TRD) of the lherzolites range from 0.15 to 1.08 Ga, whereas the clinopyroxene-poor lherzolites have TRD ages of 0.64-1.67 Ga. This suggests the co-existence of Phanerozoic and Proterozoic mantle beneath the western Cathyasia block. Alternatively, the whole lithospheric mantle beneath Maguan was likely formed during the Phanerozoic, given the resemblance of their Os isotopic ratios with those of abyssal peridotites. The latter explanation is consistent with the fact that all the studied samples plot along the oceanic trend in a plot of olivine modes versus Fo contents. We suggest that the enriched mantle that was existed beneath the western Cathyasia block during the Late Cretaceous or Eocene-Oligocene has been replaced by juvenile and depleted mantle, which probably occurred during the Cenozoic.

Total meltwater volume since the Last Glacial Maximum and viscosity structure of Earth's mantle inferred from relative sea level changes at Barbados and Bonaparte Gulf and GIA-induced J˙2

NASA Astrophysics Data System (ADS)

Nakada, Masao; Okuno, Jun'ichi; Yokoyama, Yusuke

2016-02-01

Inference of globally averaged eustatic sea level (ESL) rise since the Last Glacial Maximum (LGM) highly depends on the interpretation of relative sea level (RSL) observations at Barbados and Bonaparte Gulf, Australia, which are sensitive to the viscosity structure of Earth's mantle. Here we examine the RSL changes at the LGM for Barbados and Bonaparte Gulf ({{RSL}}_{{L}}^{{{Bar}}} and {{RSL}}_{{L}}^{{{Bon}}}), differential RSL for both sites (Δ {{RSL}}_{{L}}^{{{Bar}},{{Bon}}}) and rate of change of degree-two harmonics of Earth's geopotential due to glacial isostatic adjustment (GIA) process (GIA-induced J˙2) to infer the ESL component and viscosity structure of Earth's mantle. Differential RSL, Δ {{RSL}}_{{L}}^{{{Bar}},{{Bon}}} and GIA-induced J˙2 are dominantly sensitive to the lower-mantle viscosity, and nearly insensitive to the upper-mantle rheological structure and GIA ice models with an ESL component of about (120-130) m. The comparison between the predicted and observationally derived Δ {{RSL}}_{{L}}^{{{Bar}},{{Bon}}} indicates the lower-mantle viscosity higher than ˜2 × 1022 Pa s, and the observationally derived GIA-induced J˙2 of -(6.0-6.5) × 10-11 yr-1 indicates two permissible solutions for the lower mantle, ˜1022 and (5-10) × 1022 Pa s. That is, the effective lower-mantle viscosity inferred from these two observational constraints is (5-10) × 1022 Pa s. The LGM RSL changes at both sites, {{RSL}}_{{L}}^{{{Bar}}} and {{RSL}}_{{L}}^{{{Bon}}}, are also sensitive to the ESL component and upper-mantle viscosity as well as the lower-mantle viscosity. The permissible upper-mantle viscosity increases with decreasing ESL component due to the sensitivity of the LGM sea level at Bonaparte Gulf ({{RSL}}_{{L}}^{{{Bon}}}) to the upper-mantle viscosity, and inferred upper-mantle viscosity for adopted lithospheric thicknesses of 65 and 100 km is (1-3) × 1020 Pa s for ESL˜130 m and (4-10) × 1020 Pa s for ESL˜125 m. The former solution of (1-3) × 1020 Pa s is consistent with the inferences from the postglacial differential RSL changes in the Australian region and also inversion study of far-field sea-level data. The inference of the viscosity structure based on these four observational constraints is, however, relatively insensitive to the viscosity structure of D″ layer.

A global geochemical model for the evolution of the mantle

NASA Technical Reports Server (NTRS)

Anderson, D. L.

1979-01-01

It is proposed that the upper mantle transition region, 220 to 670 km, is composed of eclogite which has been derived from primitive mantle by about 20 percent partial melting and that this is the source and sink of oceanic crust. The remainder of the upper mantle is garnet peridotite which is the source of continental basalts and hotspot magmas. This region is enriched in incompatible elements by hydrous and CO2 rich metasomatic fluids which have depleted the underlying layers in the L.I.L. elements and L.R.E.E. The volatiles make this a low-velocity, high attenuation, low viscosity region. The eclogite layer is internally heated and its controls the convection pattern in the upper mantle. Plate tectonics is intermittent. The continental thermal anomaly at a depth of 150-220 km triggers kimberlite and carbonatite activity, alkali and flood basalt volcanism, vertical tectonics and continental breakup. Hot spots remain active after the continents leave and build the oceanic islands. Mantle plumes rise from a depth of about 220 km. Midocean ridge basalts rise from the depleted layer below this depth. Material from this layer can also be displaced upwards by subducted oceanic lithosphere to form back-arc basins.

Constraints on The Coupled Thermal Evolution of the Earth's Core and Mantle, The Age of The Inner Core, And The Origin of the 186Os/188Os Core(?) Signal in Plume-Derived Lavas

NASA Astrophysics Data System (ADS)

Lassiter, J. C.

2005-12-01

Thermal and chemical interaction between the core and mantle has played a critical role in the thermal and chemical evolution of the Earth's interior. Outer core convection is driven by core cooling and inner core crystallization. Core/mantle heat transfer also buffers mantle potential temperature, resulting in slower rates of mantle cooling (~50-100 K/Ga) than would be predicted from the discrepancy between current rates of surface heat loss (~44 TW) and internal radioactive heat production (~20 TW). Core/mantle heat transfer may also generate thermal mantle plumes responsible for ocean island volcanic chains such as the Hawaiian Islands. Several studies suggest that mantle plumes, in addition to transporting heat from the core/mantle boundary, also carry a chemical signature of core/mantle interaction. Elevated 186Os/188Os ratios in lavas from Hawaii, Gorgona, and in the 2.8 Ga Kostomuksha komatiites have been interpreted as reflecting incorporation of an outer core component with high time-integrated Pt/Os and Re/Os ( Brandon et al., 1999, 2003; Puchtel et al., 2005). Preferential partitioning of Os relative to Re and Pt into the inner core during inner core growth may generate elevated Re/Os and Pt/Os ratios in the residual outer core. Because of the long half-life of 190Pt (the parent of 186Os, t1/2 = 489 Ga), an elevated 186Os/188Os outer core signature in plume lavas requires that inner core crystallization began early in Earth history, most likely prior to 3.5 Ga. This in turn requires low time-averaged core/mantle heat flow (<~2.5 TW) or large quantities of heat-producing elements in the core. Core/mantle heat flow may be estimated using boundary-layer theory, by measuring the heat transported in mantle plumes, by estimating the heat transported along the outer core adiabat, or by comparing the rates of heat production, surface heat loss, and secular cooling of the mantle. All of these independent methods suggest time-averaged core/mantle heat flow of ~5-14 TW. In the absence of heat-producing elements in the core, such high heat flow rates require an inner core younger than ~1 Ga and preclude the development of significant 186Os enrichment in the outer core. Experimental studies suggest that potassium may partition into Fe-S-O liquids during core formation. Radioactive decay of potassium in the core could provide an additional heat source and reconcile geophysical evidence for high core/mantle heat flow with apparent geochemical evidence for an ancient inner core. However, high concentrations of chalcophile elements such as Cu in the mantle are inconsistent with significant segregation of a S-rich liquid during core formation, precluding K partitioning into the core by this mechanism. Furthermore, core formation scenarios that would lead to high K content in the core (e.g., core formation prior to terrestrial volatile depletion) also result in high core Pb concentrations. Core/mantle interaction would then produce strong negative correlations between 186Os/188Os and 207Pb/204Pb ratios, but such correlations are not observed. In summary, elevated 186Os/188Os ratios in some plume-derived lavas are unlikely to reflect core/mantle interaction because the inner core is too young for this isotopic signature to have developed in the outer core. Melt generation from pyroxenite or fractionation of PGEs between sulfide melts and monosulfide solid solutions provide alternative mechanisms for generating ancient mantle reservoirs with elevated Pt/Os and 186Os/188Os.

Interstellar Processes Leading to Molecular Deuterium Enrichment and Their Detection

NASA Technical Reports Server (NTRS)

Sandford, Scott A.; Kliss, Mark (Technical Monitor)

2001-01-01

Large deuterium (D) enrichments in meteoritic materials indicate that interstellar organic materials survived incorporation into parent bodies within the forming Solar System. These enrichments are likelier due to one or more of four distinct astrochemical processes. These are (1) low temperature gas phase ion-molecule reactions; (2) low temperature gas-grain reactions; (3) gas phase unimolecular photodissociation, and (4) ultraviolet photolysis in D-enriched ice mantles. Each of these processes should be associated with molecular carriers having, distinct regiochemical signatures (D placement on the product molecules, correlation with specific chemical functionalities, etc.). These processes are reviewed and specific spectroscopic signatures for the detection of these processes in space are identified and described.

Generation and Evolution of Quaternary Magmas Beneath Tengchong: Sr-Nd-Pb-Hf Isotope and Zircon U-series Age Constraints

NASA Astrophysics Data System (ADS)

Zou, H.; Ma, M.; Fan, Q.; Xu, B.; Li, S. Q.; Zhao, Y.; King, D. T., Jr.

2017-12-01

The Tengchong volcanic field on the southeastern margin of the Tibetan Plateau represents rare Quaternary volcanic eruptions on the plateau. The Quaternary Tengchong volcanic field formed high-potassium calc-alkaline volcanic rocks that include trachybasalts, basaltic trachyandesites, trachyandesites, and dacites. Herein, we present comprehensive Nd-Sr-Pb-Hf isotopic and elemental data for trachybasalts, basaltic trachyandesites, and trachyandesites from four young Tengchong volcanoes at Maanshan, Dayingshan, Heikongshan, and Laoguipo, in order to understand their magma genesis and evolution. Nd-Sr-Pb-Hf isotopes for the primitive Tengchong magma (trachybasalts with SiO2 <52.5 wt. % and MgO >5.5% wt. %) reflect a heterogeneous enriched mantle source. High Th/U, Th/Ta, and Rb/Nb ratios and Nd-Sr-Pb-Hf isotope characteristics of the primitive magmas suggest that the enriched mantle beneath Tengchong formed as a result of subduction of clay-rich sediments, which probably came from the Indian continental plate. Partial melting of the enriched mantle was generated by deep continental subduction coupled with recent regional extension in the Tengchong area. With regard to the evolved magmas (basaltic trachyandesites and trachyandesites), good correlations between SiO2 content and the ratios 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb, and 177Hf/176Hf strongly suggest that the combined assimilation and fractional crystallization (AFC) was an important process during magma evolution to form these basaltic trachyandesites and trachyandesites. Uranium-series zircon dating on these evolved lavas from Tengchong is used to constrain their magma evolution and residence timescales.

The evolution of Mercury's crust: a global perspective from MESSENGER.

PubMed

Denevi, Brett W; Robinson, Mark S; Solomon, Sean C; Murchie, Scott L; Blewett, David T; Domingue, Deborah L; McCoy, Timothy J; Ernst, Carolyn M; Head, James W; Watters, Thomas R; Chabot, Nancy L

2009-05-01

Mapping the distribution and extent of major terrain types on a planet's surface helps to constrain the origin and evolution of its crust. Together, MESSENGER and Mariner 10 observations of Mercury now provide a near-global look at the planet, revealing lateral and vertical heterogeneities in the color and thus composition of Mercury's crust. Smooth plains cover approximately 40% of the surface, and evidence for the volcanic origin of large expanses of plains suggests that a substantial portion of the crust originated volcanically. A low-reflectance, relatively blue component affects at least 15% of the surface and is concentrated in crater and basin ejecta. Its spectral characteristics and likely origin at depth are consistent with its apparent excavation from a lower crust or upper mantle enriched in iron- and titanium-bearing oxides.

Noble gases in submarine pillow basalt glasses from Loihi and Kilauea, Hawaii: A solar component in the Earth

USGS Publications Warehouse

Honda, M.; McDougall, I.; Patterson, D.B.; Doulgeris, A.; Clague, D.A.

1993-01-01

Noble gas elemental and isotopic abundances have been analysed in twenty-two samples of basaltic glass dredged from the submarine flanks of two currently active Hawaiian volcanoes, Loihi Seamount and Kilauea. Neon isotopic ratios are enriched in 20Ne and 21Ne by as much as 16% with respect to atmospheric ratios. All the Hawaiian basalt glass samples show relatively high 3He 4He ratios. The high 20Ne 22Ne values in some of the Hawaiian samples, together with correlations between neon and helium systematics, suggest the presence of a solar component in the source regions of the Hawaiian mantle plume. The solar hypothesis for the Earth's primordial noble gas composition can account for helium and neon isotopic ratios observed in basaltic glasses from both plume and spreading systems, in fluids in continental hydrothermal systems, in CO2 well gases, and in ancient diamonds. These results provide new insights into the origin and evolution of the Earth's atmosphere. ?? 1993.

Steady state toroidal magnetic field at earth's core-mantle boundary

NASA Technical Reports Server (NTRS)

Levy, Eugene H.; Pearce, Steven J.

1991-01-01

Measurements of the dc electrical potential near the top of earth's mantle have been extrapolated into the deep mantle in order to estimate the strength of the toroidal magnetic field component at the core-mantle interface. Recent measurements have been interpreted as indicating that at the core-mantle interface, the magnetic toroidal and poloidal field components are approximately equal in magnitude. A motivation for such measurements is to obtain an estimate of the strength of the toroidal magnetic field in the core, a quantity important to our understanding of the geomagnetic field's dynamo generation. Through the use of several simple and idealized calculation, this paper discusses the theoretical relationship between the amplitude of the toroidal magnetic field at the core-mantle boundary and the actual amplitude within the core. Even with a very low inferred value of the toroidal field amplitude at the core-mantle boundary, (a few gauss), the toroidal field amplitude within the core could be consistent with a magnetohydrodynamic dynamo dominated by nonuniform rotation and having a strong toroidal magnetic field.

The Evolution of Floreana Island, Galapagos: Mantle Metasomatism as a Control of Structural and Geochemical Variations

NASA Astrophysics Data System (ADS)

Koleszar, A. M.; Rollins, N. A.; Harpp, K. S.; Geist, D. J.

2004-05-01

Floreana, the 6th largest island in the Galapagos Archipelago, is situated ESE of the current proposed location of the hotspot, believed to be near Fernandina Island. Floreana is the most distant Galapagos volcano from the Galapagos Spreading Center and is located on 12 Ma lithosphere. Both normally- and reversely-polarized flows are present on Floreana, which emerged more than 1 Ma. The emergent shield is constructed of lava flows and >80 cinder cones. In the final stage of island building, approximately 0.3 Ma, the eruptive activity on Floreana became more explosive and produced the largest cinder cones on the island. Spatter ramparts, cinder cones, vents, and pit craters are arranged in at least 3 major parallel to sub-parallel alignments oriented N40E. The basalts of Floreana are notably alkalic, primitive, and highly enriched in incompatible trace elements (ITE). MgO concentrations in the lavas range from <8 wt% to >13 wt%, and many of the magmas are likely related by fractional crystallization of olivine and clinopyroxene. The volcano has erupted ultramafic xenoliths, which are observed predominantly in the older, reversely-polarized flows and cones. Floreana lavas have the greatest light REE enrichment observed in the archipelago and the most radiogenic Sr- and Pb- isotopic ratios, indicative of an ITE-enriched source. Elevated ratios of alkali and alkaline earth contents to those of high-field strength elements indicate contributions from metasomatic fluids to Floreana melts. Although the effects of metasomatism are apparent in most Floreana basalts, normally-polarized lavas may have been affected to a greater extent by the metasomatism than the older flows. Temporal-compositional trends in trace element concentrations also suggest that the depth of melt generation may have decreased slightly over the course of the island's formation. Floreana is distinct from the rest of the Galapagos Archipelago in its explosive history, abundant mantle xenoliths, extensive evidence for contributions from metasomatic fluids, and ITE-enriched composition of its mantle source. We propose that the ubiquitous metasomatic processes may be responsible for both the structural and geochemical anomalies observed on Floreana and may be the primary distinguishing characteristic of this end-member in Galapagos mantle plume compositions.

Sources and mobility of carbonate melts beneath cratons, with implications for deep carbon cycling, metasomatism and rift initiation

NASA Astrophysics Data System (ADS)

Tappe, Sebastian; Romer, Rolf L.; Stracke, Andreas; Steenfelt, Agnete; Smart, Katie A.; Muehlenbachs, Karlis; Torsvik, Trond H.

2017-05-01

Kimberlite and carbonatite magmas that intrude cratonic lithosphere are among the deepest probes of the terrestrial carbon cycle. Their co-existence on thick continental shields is commonly attributed to continuous partial melting sequences of carbonated peridotite at >150 km depths, possibly as deep as the mantle transition zone. At Tikiusaaq on the North Atlantic craton in West Greenland, approximately 160 Ma old ultrafresh kimberlite dykes and carbonatite sheets provide a rare opportunity to study the origin and evolution of carbonate-rich melts beneath cratons. Although their Sr-Nd-Hf-Pb-Li isotopic compositions suggest a common convecting upper mantle source that includes depleted and recycled oceanic crust components (e.g., negative ΔεHf coupled with > + 5 ‰ δ7Li), incompatible trace element modelling identifies only the kimberlites as near-primary low-degree partial melts (0.05-3%) of carbonated peridotite. In contrast, the trace element systematics of the carbonatites are difficult to reproduce by partial melting of carbonated peridotite, and the heavy carbon isotopic signatures (-3.6 to - 2.4 ‰ δ13C for carbonatites versus -5.7 to - 3.6 ‰ δ13C for kimberlites) require open-system fractionation at magmatic temperatures. Given that the oxidation state of Earth's mantle at >150 km depth is too reduced to enable larger volumes of 'pure' carbonate melt to migrate, it is reasonable to speculate that percolating near-solidus melts of carbonated peridotite must be silicate-dominated with only dilute carbonate contents, similar to the Tikiusaaq kimberlite compositions (e.g., 16-33 wt.% SiO2). This concept is supported by our findings from the North Atlantic craton where kimberlite and other deeply derived carbonated silicate melts, such as aillikites, exsolve their carbonate components within the shallow lithosphere en route to the Earth's surface, thereby producing carbonatite magmas. The relative abundances of trace elements of such highly differentiated 'cratonic carbonatites' have only little in common with those of metasomatic agents that act on the deeper lithosphere. Consequently, carbonatite trace element systematics should only be used with caution when constraining carbon mobility and metasomatism at mantle depths. Regardless of the exact nature of carbonate-bearing melts within the mantle lithosphere, they play an important role in enrichment processes, thereby decreasing the stability of buoyant cratons and promoting rift initiation - as exemplified by the Mesozoic-Cenozoic breakup of the North Atlantic craton.

The Paradox of a Wet (High H2O) and Dry (Low H2O/Ce) Mantle: High Water Concentrations in Mantle Garnet Pyroxenites from Hawaii

NASA Technical Reports Server (NTRS)

Peslier, Anne H.; Bizimis, Michael

2013-01-01

Water dissolved as trace amounts in anhydrous minerals has a large influence on the melting behavior and physical properties of the mantle. The water concentration of the oceanic mantle is inferred from the analyses of Mid-Ocean Ridge Basalt (MORB) and Oceanic Island Basalt (OIB). but there is little data from actual mantle samples. Moreover, enriched mineralogies (pyroxenites, eclogites) are thought as important sources of heterogeneity in the mantle, but their water concentrations and their effect on the water budget and cycling in the mantle are virtually unknown. Here, we analyzed by FTIR water in garnet clinopyroxenite xenoliths from Salt Lake Crater, Oahu, Hawaii. These pyroxenites are high-pressure (>20kb) crystal fractionates from alkalic melts. The clinopyroxenes (cpx) have 260 to 576 ppm wt H2O, with the least differentiated samples (Mg#>0.8) in the 400-500 ppm range. Orthopyroxene (opx) contain 117-265 ppm H2O, about half of that of cpx, consistent with other natural sample studies, but lower than cpx/opx equilibrium from experimental data. The pyroxenite cpx and opx H2O concentrations are at the high-end of on-and off-craton peridotite xenolith concentrations and those of Hawaiian spinel peridotites. In contrast, garnet has extremely low water contents (<5ppm H2O). There is no correlation between H2O in cpx and lithophile element concentrations. Phlogopite is present in some samples, and its modal abundance shows a positive correlation in Mg# with cpx, implying equilibrium. However, there is no correlation between H2O concentrations and or the presence of phlogopite. These data imply that cpx and opx may be at water saturation, far lower than experimental data suggest. Reconstructed bulk rock pyroxenite H2O ranges from 200-460 ppm (average 331 +/- 75 ppm), 2 to 8 times higher than H2O estimates for the MORB source (50-200 ppm), but in the range of E-MORB, OIB and the source of rejuvenated Hawaiian magmas. The average bulk rock pyroxenite H2O/Ce is 69 +/-35, lower than estimates of the MORB source (approx 150) or FOZO, C (200-250) mantle component, but consistent with "dry" EM sources (<100). These data suggest that a metasomatized, refertilized oceanic lithosphere that contains pyroxenitic veins (e.g. the lower part of an oceanic plate, where ascending melts can become trapped and crystallize), will have both higher water concentrations and low H2O/Ce, and may contribute to EM-type OIB sources, like that of Samoa basalts. Therefore, a low H2O/Ce mantle source may not necessarily be "dry".

Can a fractionally crystallized magma ocean explain the thermo-chemical evolution of Mars?

NASA Astrophysics Data System (ADS)

Plesa, A.-C.; Tosi, N.; Breuer, D.

2014-10-01

The impact heat accumulated during the late stage of planetary accretion can melt a significant part or even the entire mantle of a terrestrial body, giving rise to a global magma ocean. The subsequent cooling of the interior causes the magma ocean to freeze from the core-mantle boundary (CMB) to the surface due to the steeper slope of the mantle adiabat compared to the slope of the solidus. Assuming fractional crystallization of the magma ocean, dense cumulates are produced close to the surface, largely due to iron enrichment in the evolving magma ocean liquid. A gravitationally unstable mantle thus forms, which is prone to overturn. We investigate the cumulate overturn and its influence on the thermal evolution of Mars using mantle convection simulations in 2D cylindrical geometry. We present a suite of simulations using different initial conditions and a strongly temperature-dependent viscosity. We assume that all radiogenic heat sources have been enriched during the freezing-phase of the magma ocean in the uppermost 50 km and that the initial steam-atmosphere created by the degassing of the freezing magma ocean was rapidly lost, implying that the surface temperature is set to present-day values. In this case, a stagnant lid quickly forms on top of the convective interior preventing the uppermost dense cumulates to sink, even when allowing for a plastic yielding mechanism. Below this dense stagnant lid, the mantle chemical gradient settles to a stable configuration. The convection pattern is dominated by small-scale structures, which are difficult to reconcile with the large-scale volcanic features observed over Mars' surface and partial melting ceases in less than 900 Ma. Assuming that the stagnant lid can break because of additional mechanisms and allowing the uppermost dense layer to overturn, a stable density gradient is obtained, with the densest material and the entire amount of heat sources lying above the CMB. This stratification leads to a strong overheating of the lowermost mantle, whose temperature increases to values that exceed the liquidus. The iron-rich melt would most likely remain trapped in the lower part of the mantle. The upper mantle in that scenario cools rapidly and only shows partial melting during the first billion year of evolution. Therefore a fractionated global and deep magma ocean is difficult to reconcile with observations. Different scenarios assuming, for instance, a hemispherical or shallow magma ocean, or a crystallization sequence resulting in a lower density gradient than that implied by pure fractional crystallization will have to be considered.

Temporal Variations in the Mantle Source of MORB near the Vema Fracture Zone (Central Atlantic): Nd and Sr Isotopes in Peridotites and Basaltic Glasses

NASA Astrophysics Data System (ADS)

Cipriani, A.; Cipriani, A.; Brunelli, D.; Brueckner, H. K.; Brueckner, H. K.; Bonatti, E.; Bonatti, E.

2001-12-01

Sr-Nd-Pb isotopic ratios of zero age basalts sampled along Mid-Ocean Ridges (MOR) have demonstrated that the mantle is heterogeneous at a regional scale. However, how the mantle evolves through time below a single segment of MOR it is still matter of debate. Peridotites and basaltic glasses were collected along a lithospheric section uplifted and exposed on the southern side of the Vema transform (10o North, Atlantic Ocean) along a seafloor spreading flow line for a stretch of almost 200 km (corresponding to roughly 10 my). This set of samples offers a unique opportunity to detect changes through time of the mantle signature in a segment of Mid Atlantic Ridge, by analyzing radiogenic isotopes in the clinopyroxenes (cpx) from peridotites and glasses from the overlying basalts. Work is in progress; initial Sr and Nd measurements from cpxs within peridotites indicate several things. First, the cpxs display "depleted" mantle signatures. Second, there is a considerable variation of the isotopic ratios along the exposed section (143Nd/144Nd varies from 0.51293 to 0.51345, 87Sr/86Sr varies from 0.70228 to 0.70422) and these variations occur over a short time scale (some occur within an interval of one million year). Next, the Sr and Nd ratios are inversely correlated and fall along the mantle array. Finally, cpx Nd ratios are inversely correlated with the Cr/Al ratio of the spinel and ortopyroxene (opx) from the peridotites while Sr ratios are positively correlated. Thus, the chemically most depleted peridotite with high Cr/Al ratios show the most enriched isotopic signatures, a pattern that has also been observed in alpine-type peridotites and peridotite nodules and that is generally interpreted as metasomatism by enriched fluids affecting depleted peridotite more extensively than less depleted peridotite. This may indicate that the temporal variations in the extent of melting detected by Cr/Al ratio in spinel and opx (Bonatti et al., Variations with age of mantle ultramafic composition near the Vema Fracture Zone, Central Atlantic. EOS, Vol.79, No.45, F919) are related to rapid changes in the degree of depletion of the upwelling mantle sources and that the degree of depletion of these mantle sources is an inherited feature from earlier processes rather than the result of melting at the MOR.

Evidence from coupled (Sm-147)-(Nd-143) and (Sm-146)-(Nd-142) systematics for very early (4.5-Gyr) differentiation of the earth's mantle

NASA Technical Reports Server (NTRS)

Harper, Charles L., Jr.; Jacobsen, Stein B.

1992-01-01

Evidence for early differentiation of the earth's mantle is presented based on measurements of Nd-143/Nd-144 and Nd-142/Nd-144 ratios in an approximately 3.8 Gyr-old supracrustal rock from Isua, West Greenland. Coupled (Sm-146,147)-(Nd-142,143) systematics suggest that the fractionation of Sm/Nd took place 4.44-4.54 Gyr ago, due to extraction of a light rare earth element-enriched primordial crust.

Mantle upwellings and convective instabilities revealed by seismic tomography and helium isotope geochemistry beneath eastern Africa

NASA Astrophysics Data System (ADS)

Montagner, Jean-Paul; Marty, Bernard; Stutzmann, Eléonore; Sicilia, Déborah; Cara, Michel; Pik, Raphael; Lévêque, Jean-Jacques; Roult, Geneviève; Beucler, Eric; Debayle, Eric

2007-11-01

The relationship between intraplate volcanism and continental tectonics has been investigated for North and East Africa using a high resolution three-dimensional anisotropic tomographic model derived from seismic data of a French experiment ``Horn of Africa'' and existing broadband data. The joint inversion for seismic velocity and anisotropy of the upper 400 km of the mantle, and geochemical data reveals a complex interaction between mantle upwellings, and lithosphere. Two kinds of mantle upwellings can be distinguished: The first one, the Afar ``plume'' originates from deeper than 400 km and is characterized by enrichment in primordial 3He and 3He/4He ratios higher than those along mid-ocean ridges (MOR). The second one, associated with other Cenozoic volcanic provinces (Darfur, Tibesti, Hoggar, Cameroon), with 3He/4He ratios similar to, or lower than MOR, is a consequence of shallower upwelling. The presumed asthenospheric convective instabilities are oriented in an east-west direction, resulting from interaction between south-north asthenospheric mantle flow, main plume head and topography on the base of lithosphere.

Growth of continental crust: Clues from Nd isotopes and Nb-Th relationships in mantle-derived magmas

NASA Astrophysics Data System (ADS)

Arndt, N. T.; Chauvel, C.; Jochum, K.-P.; Gruau, G.; Hofmann, A. W.

Isotope and trace element geochemistry of Precambrian mantle derived rocks and implications for the formation of the continental crust is discussed. Epsilon Nd values of Archean komatiites are variable, but range up to at least +5, suggesting that the Archean mantle was heterogeneous and, in part, very depleted as far back as 3.4 to 3.5 Ga. This may be taken as evidence for separation of continental crust very early in Earth history. If these komatiite sources were allowed to evolve in a closed system, they would produce modern day reservoirs with much higher epsilon Nd values than is observed. This implies recycling of some sort of enriched material, perhaps subducted sediments, although other possibilities exist. Archean volcanics show lower Nb/Th than modern volcanics, suggesting a more primitive mantle source than that observed nowadays. However, Cretaceous komatiites from Gorgona island have similar Nb/Th to Archean volcanics, indicating either the Archean mantle source was indeed more primitive, or Archean magmas were derived from a deep ocean island source like that proposed for Gorgona.

Comment on "A non-primitive origin of near-chondritic Ssbnd Sesbnd Te ratios in mantle peridotites: Implications for the Earth's late accretionary history" by König S. et al. [Earth Planet. Sci. Lett. 385 (2014) 110-121

NASA Astrophysics Data System (ADS)

Wang, Zaicong; Becker, Harry

2015-05-01

The abundances and ratios of S, Se and Te in rocks from the Earth's mantle may yield valuable constraints on the partitioning of these chalcophile elements between the mantle and basaltic magmas and on the compositions of these elements in the primitive mantle (PM) (e.g. Wang and Becker, 2013). Recently, König et al. (2014) proposed a model in which the CI chondrite-like Se/Te of mantle lherzolites (Se /Te = 8 ± 2, 1σ) are explained by mixing of sulfide melts with low Se/Te with harzburgites containing supposedly residual sulfides with high Se/Te. In this model sulfide melts and platinum group element (PGE) rich telluride phases with low Se/Te are assumed to have precipitated during refertilization of harzburgites by basic melts to form lherzolites. Because of the secondary nature of these re-enrichment processes, the authors state that abundances and ratios of S, Se and Te in fertile lherzolites cannot reflect the composition of the PM.

Growth of continental crust: Clues from Nd isotopes and Nb-Th relationships in mantle-derived magmas

NASA Technical Reports Server (NTRS)

Arndt, N. T.; Chauvel, C.; Jochum, K.-P.; Gruau, G.; Hofmann, A. W.

1988-01-01

Isotope and trace element geochemistry of Precambrian mantle derived rocks and implications for the formation of the continental crust is discussed. Epsilon Nd values of Archean komatiites are variable, but range up to at least +5, suggesting that the Archean mantle was heterogeneous and, in part, very depleted as far back as 3.4 to 3.5 Ga. This may be taken as evidence for separation of continental crust very early in Earth history. If these komatiite sources were allowed to evolve in a closed system, they would produce modern day reservoirs with much higher epsilon Nd values than is observed. This implies recycling of some sort of enriched material, perhaps subducted sediments, although other possibilities exist. Archean volcanics show lower Nb/Th than modern volcanics, suggesting a more primitive mantle source than that observed nowadays. However, Cretaceous komatiites from Gorgona island have similar Nb/Th to Archean volcanics, indicating either the Archean mantle source was indeed more primitive, or Archean magmas were derived from a deep ocean island source like that proposed for Gorgona.

Rare gas isotopes and parent trace elements in ultrabasic-alkaline-carbonatite complexes, Kola Peninsula: identification of lower mantle plume component

NASA Astrophysics Data System (ADS)

Tolstikhin, I. N.; Kamensky, I. L.; Marty, B.; Nivin, V. A.; Vetrin, V. R.; Balaganskaya, E. G.; Ikorsky, S. V.; Gannibal, M. A.; Weiss, D.; Verhulst, A.; Demaiffe, D.

2002-03-01

During the Devonian magmatism (370 Ma ago) ∼20 ultrabasic-alkaline-carbonatite complexes (UACC) were formed in the Kola Peninsula (north-east of the Baltic Shield). In order to understand mantle and crust sources and processes having set these complexes, rare gases were studied in ∼300 rocks and mineral separates from 9 UACC, and concentrations of parent Li, K, U, and Th were measured in ∼70 samples. 4He/3He ratios in He released by fusion vary from pure radiogenic values ∼108 down to 6 × 104. The cosmogenic and extraterrestrial sources as well as the radiogenic production are unable to account for the extremely high abundances of 3He, up to 4 × 10-9 cc/g, indicating a mantle-derived fluid in the Kola rocks. In some samples helium extracted by crushing shows quite low 4He/3He = 3 × 104, well below the mean ratio in mid ocean ridge basalts (MORB), (8.9 ± 1.0) × 104, indicating the contribution of 3He-rich plume component. Magnetites are principal carriers of this component. Trapped 3He is extracted from these minerals at high temperatures 1100°C to 1600°C which may correspond to decrepitation or annealing primary fluid inclusions, whereas radiogenic 4He is manly released at a temperature range of 500°C to 1200°C, probably corresponding to activation of 4He sites degraded by U, Th decay. Similar 4He/3He ratios were observed in Oligocene flood basalts from the Ethiopian plume. According to a paleo-plate-tectonic reconstruction, 450 Ma ago the Baltica (including the Kola Peninsula) continent drifted not far from the present-day site of that plume. It appears that both magmatic provinces could relate to one and the same deep-seated mantle source. The neon isotopic compositions confirm the occurrence of a plume component since, within a conventional 20Ne/22Ne versus 21Ne/22Ne diagram, the regression line for Kola samples is indistinguishable from those typical of plumes, such as Loihi (Hawaii). 20Ne/22Ne ratios (up to 12.1) correlate well with 40Ar/36Ar ones, allowing to infer a source 40Ar/36Ar ratio of about 4000 for the mantle end-member, which is 10 times lower than that of the MORB source end-member. In (3He/22Ne)PRIM versus (4He/21Ne)RAD plot the Kola samples are within array established for plume and MORB samples; almost constant production ratio of (4He/21Ne)RAD ≅ 2 × 107 is translated via this array into (3He/22Ne)PRIM ∼ 10. The latter value approaches the solar ratio implying the non-fractionated solar-like rare gas pattern in a plume source. The Kola UACC show systematic variations in the respective contributions of in situ-produced radiogenic isotopes and mantle-derived isotopes. Since these complexes were essentially plutonic, we propose that the depth of emplacement exerted a primary control on the retention of both trapped and radiogenic species, which is consistent with geological observations. The available data allow to infer the following sequence of processes for the emplacement and evolution of Kola Devonian UACC: 1) Ascent of the plume from the lower mantle to the subcontinental lithosphere; the plume triggered mantle metasomatism not later than ∼700 to 400 Ma ago. 2) Metasomatism of the lithosphere (beneath the central part of the Kola Peninsula), including enrichment in volatile (e.g., He, Ne) and in incompatible (e.g., U, Th) elements. 3) Multistage intrusions of parental melts, their degassing, and crystallisation differentiation ∼370 Ma ago. 4) Postcrystallisation migration of fluids, including loss of radiogenic and of trapped helium. Based on model compositions of the principle terrestrial reservoirs we estimate the contributions (by mass) of the plume material, the upper mantle material, and the atmosphere (air-saturated groundwater), into the source of parent melt at ∼2%, 97.95%, and ∼0.05%, respectively.

The influence of a subduction component on magmatism in the Okinawa Trough: Evidence from thorium and related trace element ratios

NASA Astrophysics Data System (ADS)

Guo, Kun; Zeng, Zhi-Gang; Chen, Shuai; Zhang, Yu-Xiang; Qi, Hai-Yan; Ma, Yao

2017-09-01

The Okinawa Trough (OT) is a back-arc, initial continental marginal sea basin located behind the Ryukyu Arc-Trench System. Formation and evolution of the OT have been intimately related to subduction of the Philippine Sea Plate (PSP) since the late Miocene; thus, the magma source of the trough has been affected by subduction components, as in the case of other active back-arc basins, including the Lau Basin (LB) and Mariana Trough (MT). We review all the available geochemical data relating to basaltic lavas from the OT and the middle Ryukyu Arc (RA) in this paper in order to determine the influence of the subduction components on the formation of arc and back-arc magmas within this subduction system. The results of this study reveal that the abundances of Th in OT basalts (OTBs) are higher than that in LB (LBBs) and MT basalts (MTBs) due to the mixing of subducted sediments and EMI-like enriched materials. The geochemical characteristics of Th and other trace element ratios indicate that the OTB originated from a more enriched mantle source (compared to N-mid-ocean ridge basalt, N-MORB) and was augmented by subducted sediments. Data show that the magma sources of the south OT (SOT) and middle Ryukyu Arc (MRA) basalts were principally influenced by subducted aqueous fluids and bulk sediments, which were potentially added into magma sources by accretion and underplating. At the same time, the magma sources of the middle OT (MOT) and Kobi-syo and Sekibi-Syo (KBS+SBS) basalts were impacted by subducted aqueous fluids from both altered oceanic crust (AOC) and sediment. The variable geochemical characteristics of these basalts are due to different Wadati-Benioff depths and tectonic environments of formation, while the addition of subducted bulk sediment to SOT and MRA basalts may be due to accretion and underplating, and subsequent to form mélange formation, which would occur partial melting after aqueous fluids are added. The addition of AOC and sediment aqueous fluid to MOT and KBS+SBS basalts is therefore the result of cold subducted slab dehydration combined with a rapid subduction rate (82 mm/a), leading to the migration of fluids into the mantle wedge. The presence of these attributes is likely because the OT was a back-arc, initial continental marginal sea basin.

Two-pyroxene syenitoids from the Moldanubian Zone of the Bohemian Massif: peculiar magmas derived from a strongly enriched lithospheric mantle source

NASA Astrophysics Data System (ADS)

Janoušek, Vojtěch; Holub, František; Gerdes, Axel; Verner, Kryštof

2013-04-01

(Ultra-)potassic plutonic rocks constitute a conspicuous association with metamorphic rocks of the high-grade, lower crustal/upper mantle Gföhl Unit (Moldanubian Zone). They can be subdivided into two contrasting suites: (1) coarse Kfs-phyric amphibole-biotite melagranite to quartz syenite (the durbachite series sensu Holub 1997), and (2) essentially even-grained biotite-two-pyroxene quartz syenites to melagranites (Tábor and Jihlava plutons). The latter, "syenitoid suite", characterized by an originally 'dry' mineral assemblage orthopyroxene + clinopyroxene + Mg-biotite, with accessoric zircon, apatite, ilmenite, monazite and/or rutile ± Cr-spinel, is a subject of the current study. Our conventional U-Pb ages for zircon (336.9 ± 0.6 Ma) and rutile (336.8 ± 0.8 Ma) from the Tábor Pluton, together with the age from the Jihlava body (U-Pb zircon: 335.1 ± 0.6 Ma; Kotková et al. 2010), provide a precise time bracket for the emplacement and rapid cooling of the syenitoids below c.600 ° C (closure temperature of U-Pb system in rutile: Cherniak 2000). This is in line with post-tectonic emplacement of hot dry melt into shallow levels of essentially consolidated orogenic crust. Comparably low temperatures obtained by zircon and rutile saturation calculations document probably a delayed onset of crystallization of the accessories in a hot, alkalis and ferromagnesian components-rich magma derived from a mantle source. Indeed, the structural relations inside and around the ultrapotassic plutons suggest that the most important regional HT/LP flat-lying fabric(s) in the Moldanubian Zone are closely related with the emplacement and crystallization of the durbachite suite at 343-338 Ma. They have formed prior to the relatively shallower emplacement of the essentially post-tectonic syenitoids dated at ~337-336 Ma (Žák et al. 2005; Verner et al. 2006, 2008). The two magmatic suites are thus essentially diachronous and not (nearly) contemporaneous (c. 335 Ma) intrusions at contrasting crustal levels as assumed by Kotková et al. (2010). The syenitoid plutons show mutually comparable, crustal-like radiogenic isotope signatures with highly radiogenic Sr (87Sr/86Sr337= 0.7119-0.7125) and unradiogenic Nd (?Nd337 = -6.8 to -7.6). This, together with the rest of the whole-rock geochemical variation, is in line with a generation from a strongly enriched lithospheric mantle source. It was, shortly before, modified by a deep subduction and relamination of the upper crustal material, similar to the felsic HP granulites common in the Moldanubian Zone (Janoušek & Holub 2007; Lexa et al. 2011). The petrology and chemical data indicate that large-scale mixing with crustally-derived acid magmas can be largely or fully discounted and the key role is ascribed to closed-system fractional crystallization with, or without, crystal accumulation of various combinations of biotite, clinopyroxene and/or orthopyroxene with minor amounts of apatite. This stands in a sharp contrast with the history of volumetrically prevalent, slightly older, durbachite suite, in genesis of which the magma mixing of chemically and isotopically contrasting mantle and crustal components was clearly much more significant (Holub 1997). This research was financially supported by the GAR Project P210-11-2358 (to VJ).

Hydrous metasomatism of oceanic sub-arc mantle, Lihir, Papua New Guinea. Part 2. Trace element characteristics of slab-derived fluids

NASA Astrophysics Data System (ADS)

Grégoire, Michel; McInnes, Brent I. A.; O'Reilly, Suzanne Y.

2001-11-01

Spinel peridotite xenoliths recovered from the Tubaf and Edison volcanoes, south of Lihir Island in the Tabar-Lihir-Tanga-Feni island arc in Papua New Guinea, are predominantly fresh, refractory harzburgites. Many of the harzburgite xenoliths have cross-cutting vein networks and show evidence of modal metasomatism. These metasomatic veins contain a secondary mineral assemblage consisting of fibrous, radiating orthopyroxene and fine-grained Fe-Ni sulfide with minor olivine, clinopyroxene, phlogopite, amphibole and magnetite. Adjacent to the veins, primary clinopyroxene is cloudy while orthopyroxene exhibits replacement by secondary fibrous orthopyroxene, similar in habit to orthopyroxene occurring in the veins. The mineralogical and geochemical characteristics of the Tubaf mantle xenoliths are the product of two major processes: an early partial melting depletion event that was overprinted by oxidation and alkali enrichment related to percolation of slab-derived, hydrous melts. HREE and MREE concentrations in clinopyroxene from the least metasomatised harzburgites indicate that they are the residues from a 15% to 25% partial melting event, consistent with formation in a MOR setting. The secondary vein assemblages show strong enrichment in the LILE (primarily Sr, Ba, Rb, Th, U and Pb) and the REE (primarily La, Ce, Nd, Sm, Eu and Gd), while the HFSE (Nb, Ta, Zr, Hf, and Ti) are neither enriched nor depleted. The mineral precipitates in the vein assemblages have high LREE/HFSE and LILE/HFSE, and reflect the relative solubility of these elements in hydrous melts. These trace element characteristics are similar to those of the Tabar-Lihir-Tanga-Feni arc lavas, and display the commonly observed HFSE depletion of arc magmatism. These findings support the hypothesis that this so-called "arc signature" is primarily dependent on the relative solubility of elements in slab-derived, hydrous melts, and the enrichment of these soluble elements in metasomatised mantle regions that are prone to preferential partial melting.

Halogens in normal- and enriched-basalts from Central Indian Ridge (18-20°S): Testing the E-MORB subduction origin hypothesis

NASA Astrophysics Data System (ADS)

Ruzie, L.; Burgess, R.; Hilton, D. R.; Ballentine, C. J.

2012-12-01

Basalts emitted along oceanic ridges have often been subdivided into two categories: the Normal-MORB and the Enriched-MORB, anomalously enriched in highly incompatible elements. Donnelly et al. (2004) proposed that the formation of enriched sources is related to two stages of melting. The first one occurs in subduction zones where the mantle wedge is enriched by the addition of low-degree melts of subducted slab. The second stage of melting occurs beneath ocean ridges. Because of their incompatibility, relatively high concentrations and distinct elemental compositions in surface reservoirs, the heavy halogens (Cl, Br, I) are good tracers to detect the slab contribution in E-MORB sources. However, the halogen systematics in mantle reservoirs remains poorly constrained mainly because of their very low abundance in materials of interest. An innovative halogen analytical technique, developed at the University of Manchester, involving neutron irradiation of samples to convert halogens to noble gases provides detection limits unmatched by any other technique studies [Johnson et al. 2000]. For the first time Cl, Br and I can now be determined in appropriate samples. We focus on the content of halogens in the glassy margins of basalts erupted along the CIR from 18-20°S and the off-axis Gasitao Ridge. Our set of samples contains both N- and E-MORB and is fully described in terms of major and trace elements, as well as 3He/4He ratios and water concentrations [Murton et al., 2005; Nauret et al., 2006; Füri et al., 2011; Barry et al., in prep.]. The halogen concentration range is between 10 and 140 ppm for Cl, 30 and 500 ppb for Br and 0.8 and 10 ppb for I. The higher concentrations are found in E-MORB samples from the northern part of ridge axis. Comparing our data with previous halogen studies, our sample suites fall within the range of N-MORB from East Pacific Ridge (EPR) and Mid-Atlantic Ridge (MAR) [Jambon et al. 1995; Deruelle et al. 1992] and in the lower range of E-MORB from Macquarie Island [Kendrick et al., 2012]. The concentrations are not related to superficial processes. The on-axis samples display a relatively restricted range (6.9-8.6wt%) of MgO contents, suggesting no control of the crystallisation processes. The basalts were erupted between 3900-2000 m bsl, so no appreciable degassing of halogens would be expected. The strong correlation, which exists between the halogens and other incompatible elements (e.g., Rb, La), also rules out seawater assimilation. Therefore, concentrations and elemental ratios can be directly linked to melting and source features. Estimates of halogens abundances in the depleted-mantle source are 4 ppm Cl, 14 ppb Br and 0.3 ppb I. These low abundances, which are in agreement with values derived for sub-continental mantle from coated diamonds [Burgess et al., 2002], suggest that, like noble gases, the upper mantle is degassed of its halogens. Critically, the halogen elemental ratios show no significant variations along the axial ridge and off-axis ridge or between N-MORB and E-MORB: Br/Cl=0.00147±0.00014, I/Cl=0.000021±0.000005; I/Br=0.0142±0.0036. These ratios are similar to E-MORB from Macquarie Island [Kendrick et al., 2012]. This observation is thus not consistent with subduction as a source of halogen enrichment in E-MORB.

Multi-stage mixing in subduction zone: Application to Merapi volcano, Indonesia

NASA Astrophysics Data System (ADS)

Debaille, V.; Doucelance, R.; Weis, D.; Schiano, P.

2003-04-01

Basalts sampling subduction zone volcanism (IAB) often show binary mixing relationship in classical Sr-Nd, Pb-Pb, Sr-Pb isotopic diagrams, generally interpreted as reflecting the involvement of two components in their source. However, several authors have highlighted the presence of minimum three components in such a geodynamical context: mantle wedge, subducted and altered oceanic crust and subducted sediments. The overlying continental crust can also contribute by contamination and assimilation in magma chambers and/or during magma ascent. Here we present a multi-stage model to obtain a two end-member mixing from three components (mantle wedge, altered oceanic crust and sediments). The first stage of the model considers the metasomatism of the mantle wedge by fluids and/or melts released by subducted materials (altered oceanic crust and associated sediments), considering mobility and partition coefficient of trace elements in hydrated fluids and silicate melts. This results in the generation of two distinct end-members, reducing the number of components (mantle wedge, oceanic crust, sediments) from three to two. The second stage of the model concerns the binary mixing of the two end-members thus defined: mantle wedge metasomatized by slab-derived fluids and mantle wedge metasomatized by sediment-derived fluids. This model has been applied on a new isotopic data set (Sr, Nd and Pb, analyzed by TIMS and MC-ICP-MS) of Merapi volcano (Java island, Indonesia). Previous studies have suggested three distinct components in the source of indonesian lavas: mantle wedge, subducted sediments and altered oceanic crust. Moreover, it has been shown that crustal contamination does not significantly affect isotopic ratios of lavas. The multi-stage model proposed here is able to reproduce the binary mixing observed in lavas of Merapi, and a set of numerical values of bulk partition coefficient is given that accounts for the genesis of lavas.

Geochronology, geochemistry, and petrogenesis of late Permian to early Triassic mafic rocks from Darongshan, South China: Implications for ultrahigh-temperature metamorphism and S-type granite generation

NASA Astrophysics Data System (ADS)

Xu, Wang-Chun; Luo, Bi-Ji; Xu, Ya-Jun; Wang, Lei; Chen, Qi

2018-05-01

The role of the mantle in generating ultrahigh-temperature metamorphism and peraluminous S-type granites, and the extent of crust-mantle interaction are topics fundamental to our understanding of the Earth's evolution. In this study we present geochronological, geochemical, and Sr-Nd-Hf isotopic data for dolerites and mafic volcanic rocks from the Darongshan granite complex belt in western Cathaysia, South China. LA-ICP-MS U-Pb zircon analyses yielded magma crystallization ages of ca. 250-248 Ma for the dolerites, which are coeval with eruption of the mafic volcanic rocks, ultrahigh-temperature metamorphism, and emplacement of S-type granites in the Darongshan granite complex belt. The mafic volcanic rocks are high-K calc-alkaline or shoshonitic, enriched in Th, U, and light rare earth elements, and depleted in Nb, Ta and Ti. The dolerites are characterized by high Fe2O3tot (11.61-20.39 wt%) and TiO2 (1.62-3.17 wt%), and low MgO (1.73-4.38 wt%), Cr (2.8-10.8 ppm) and Ni (2.5-11.4 ppm). Isotopically, the mafic volcanic rocks have negative whole-rock εNd(t) values (-6.7 to -9.0) and high ISr values (0.71232 to 0.71767), which are slightly depleted compared with the dolerite samples (εNd(t) = -10.3 to -10.4 and ISr = 0.71796 to 0.71923). Zircons in the dolerites have εHf(t) values of -7.6 to -10.9. The mafic volcanic rocks are interpreted to have resulted from the partial melting of an enriched lithospheric mantle source with minor crustal contamination during ascent, whereas the dolerites formed by late-stage crystallization of enriched lithospheric mantle-derived magmas after fractionation of olivine and pyroxene. The formation of these mantle-derived mafic rocks may be attributed to transtension along a NE-trending strike-slip fault zone that was related to oblique subduction of the Paleo-Pacific plate beneath South China. Such underplated mafic magmas would provide sufficient heat for the generation of ultrahigh-temperature metamorphism and S-type granites, and act as a mafic end-member for S-type granite genesis.

Imprints of an "Arc" Signature onto Subduction Zone Eclogites from Central Guatemala

NASA Astrophysics Data System (ADS)

Simons, K. K.; Sorensen, S. S.; Harlow, G. E.; Brueckner, H. K.; Goldstein, S. L.; Hemming, N. G.; Langmuir, C. H.

2007-12-01

High-pressure, low-temperature (HP-LT) rocks associated with the Motagua fault zone in central Guatemala occur as tectonic blocks in serpentinite mélange. Dismembered jadeitite and albitite veins within the melange are crystallization products of subduction fluids at <400° C and 0.4-1.4 GPa. Lawsonite eclogites represent the deepest, coldest rocks, with peak metamorphic conditions of approx. 2.6 GPa and 480°C. They contain a subduction fluid overprint acquired during retrogression to blue- and green-schist-facies conditions, seen mostly as hydrous phases (e.g. phengite, glaucophane) in veins and overgrowths. The low temperatures recorded in these rocks indicate they have only seen an aqueous fluid, not a melt, and therefore, could provide a window into the acquisition of an arc signature at a cold margin. Trace-element patterns for both eclogite and jadeitite resemble arc lavas, with large enrichments in the most fluid mobile elements (e.g. Cs, Tl, Ba, Pb), moderate enrichments in U, Th, Be and LREE and generally little to no enrichment in HFSE and HREE, although enriched Nb in jadeitite indicates some HFSE mobility. Trace-element patterns also have similarities to average subducting sediment (GLOSS), with enrichments in Th, Be, Ba and Li that suggest a sediment contribution. Nd versus Sr isotopes lie to the right of the mantle array, indicating a hydrous fluid contribution from altered ocean crust or sediment. Overall, Guatemalan eclogites resemble counterparts from the Franciscan Complex (CA) and the Dominican Republic. Guatemalan and Franciscan eclogites are interpreted to have had a MORB protolith despite the arc trace element signature because of: 1) similarities in major elements to MORB; 2) HREE and HFSE abundances similar to MORB; and 3) high 143Nd/144Nd that overlap MORB values. The modifications that transformed these eclogites from a MORB trace element pattern to an arc one can be attributed to an aqueous subduction fluid at moderate depths (<75km). This transformation may be due to the increased solubilities of some minerals (e.g., jadeite, albite, clays, sulfates) at high pressure, high water/rock ratios from dehydration reactions, and an abundance of alkali-aluminosilicate components in subduction fluids. Together these may act to dissolve and transport trace elements (including elements considered insoluble like Nb) out of the slab and into the mantle wedge. The Guatemala data thus indicate that the arc geochemical fingerprint may be achieved at cold margins without the need for melting.

Petrogenesis of ore-bearing porphyry in non-subduction setting: a case study of the Eocene potassic intrusions in the western Yangtze Block

NASA Astrophysics Data System (ADS)

Liu, Zheng; Liao, Shi-Yong; Zhou, Qing; Zhang, Xin

2018-05-01

In the western Yangtze Block, abundant Eocene ( 38-34 Ma) potassic adakite-like intrusions and associated porphyry copper deposits are exposed in non-subduction setting, including Machangjing, Beiya, Binchuan, Habo and Tongchang intrusions. All these ore-bearing porphyries share many geochemical characteristics of adakite such as depletion in heavy rare earth elements (HREEs), enrichment in Sr and Ba, absence of negative Eu anomalies, high SiO2, Al2O3, Sr/Y, La/Yb and low Y, Yb contents. They also exhibit affinities of potassic rocks, e.g., alkali-rich, high K2O/Na2O ratios and enrichment in light rare earth elements (LREEs) and large ion lithophile elements (LILEs). Their Sr-Nd isotopic ratios are similar to coeval shoshonitic lamprophyres. Geochemical data indicate that they were probably produced by partial melting of newly underplated potassic rocks sourced from a modified and enriched lithospheric mantle. These underplated rocks have elevated oxygen fugacity, water and copper contents, with high metallogenic potential. We propose that all the studied potassic rocks were emplaced in a post-collisional setting, associated with the local removal of lithospheric mantle.

Hydrous parental magmas of Early to Middle Permian gabbroic intrusions in western Inner Mongolia, North China: New constraints on deep-Earth fluid cycling in the Central Asian Orogenic Belt

NASA Astrophysics Data System (ADS)

Pang, Chong-Jin; Wang, Xuan-Ce; Xu, Bei; Luo, Zhi-Wen; Liu, Yi-Zhi

2017-08-01

The role of fluids in the formation of the Permian-aged Xigedan and Mandula gabbroic intrusions in western Inner Mongolia was significant to the evolution of the Xing'an Mongolia Orogenic Belt (XMOB), and the active northern margin of the North China Craton (NCC). Secondary Ion Mass Spectroscopy (SIMS) U-Pb zircon geochronology establishes that the Xigedan gabbroic intrusion in the northern NCC was emplaced at 266 Ma, and is therefore slightly younger than the ca 280 Ma Mandula gabbroic intrusion in the XMOB. Along with their felsic counterparts, the mafic igneous intrusions record extensive bimodal magmatism along the northern NCC and in the XMOB during the Early to Middle Permian. The Mandula gabbroic rocks have low initial 87Sr/86Sr ratios (0.7040-0.7043) and positive εNd(t) (+6.2 to +7.3) and εHf(t) values (+13.4 to +14.5), resembling to those of contemporaneous Mandula basalts. These features, together with the presence of amphibole and the enrichment of large ion lithophile elements (LILE, e.g., Rb, Ba, U and Sr) and depletion of Nb-Ta suggest that the parental magmas of the Mandula mafic igneous rocks were derived from a depleted mantle source metasomatized by water-rich fluids. In contrast, the Xigedan gabbroic rocks are characterised by high 87Sr/86Sr ratios (0.7078-0.7080) and zircon δ18O values (5.84-6.61‰), but low εNd(t) (-9.3 to -10.2) and εHf(t) values (-8.76 to -8.54), indicative of a long-term enriched subcontinental lithosphere mantle source that was metasomatized by recycled, high δ18O crustal materials prior to partial melting. The high water contents (4.6-6.9 wt%) and arc-like geochemical signature (enrichment of fluid-mobile elements and depletion of Nb-Ta) of the parental magmas of the Xigedan gabbroic rocks further establish the existence of a mantle hydration event caused by fluid/melts released from hydrated recycled oceanic crust. Incompatible element modelling shows that 5-10% partial melting of an enriched mantle source by adding respectively 0.5% and 2% sediment melts and fluids, could have produced the parental magmas of the Xigedan gabbroic rocks. A range of geological evidence establishes an intracontinental origin for Late Paleozoic mafic igneous rocks along the northern NCC and in the XMOB, rather than a subduction-related setting. We therefore propose a deep-Earth water cycling process to account for mantle hydration and subsequent Late Paleozoic magmatism, supporting a geodynamic link between deep-Earth water cycling, and intracontinental magmatism and lithospheric extension.

Slab-derived metasomatism in the Carpathian-Pannonian mantle revealed by investigations of mantle xenoliths from the Bakony-Balaton Highland Volcanic Field

NASA Astrophysics Data System (ADS)

Créon, Laura; Delpech, Guillaume; Rouchon, Virgile; Guyot, François

2017-08-01

A suite of fifteen peridotite xenoliths from the Bakony-Balaton Highland Volcanic Field (BBHVF, Pannonian Basin, Central Europe) that show abundant petrographic evidence of fluid and melt percolation were studied in order to decipher the formation of their melt pockets and veins. The suite mainly consists of "fertile" lherzolites (5.8-19.9 vol.% clinopyroxene) and a few harzburgites (1.9-5.4 vol.% clinopyroxene) from well-known localities (Szentbékkálla, Szigliget) and two previously unreported localities (Füzes-tó and Mindszentkálla). Major and trace element data indicate that most of the peridotites record variable degrees of partial melt extraction, up to > 15% for the harzburgites. Subsequently, the xenoliths experienced at least two stages of metasomatic modification. The first stage was associated with percolation of a volatile-bearing silicate melt and resulted in crystallization of amphibole, enrichment in the most incompatible trace elements (Ba, Th, U, Sr), and development of negative Nb-Ta anomalies in clinopyroxene. The second and last metasomatic event, widespread beneath the BBHVF, is associated with the formation of silicate melt pockets, physically connected to a network of melt veins, with large and abundant CO2 vesicles. The glass in these veins has sub-alkaline trachy-andesitic composition and displays an OIB-like trace element signature. Its composition attests to the migration through a supra-subduction zone mantle wedge of silicic melt highly enriched in volatiles (CO2, H2O, Cl, F), LILE, REE and HFSE and consistent with compositions of natural and experimental examples of slab melting-derived magma. In the present case, however, melt was likely derived from melting of oceanic crust and carbonated sediments under conditions where Nb-rich mineral phases were not stable in the residue. A likely scenario for the origin such melts involves melting after subduction ceased as the slab thermally equilibrated with the asthenosphere. Melt-rock reactions due to ascent of hot, CO2-rich, siliceous melt to near-Moho depths triggered destabilization of amphibole and primary clinopyroxene, spinel, and possibly olivine. The resulting andesitic glass in melt pockets evolved to more mafic compositions due to mantle mineral assimilation but has heterogeneous trace element signatures mostly inherited from preexisting amphibole. The present example of melt-rock reactions between highly volatile-enriched siliceous slab-derived melt and peridotite from the upper part of the lithospheric mantle ultimately produced derivative melt with major element composition akin to calc-alkaline basaltic andesite, with generally low trace elements concentrations but selective pronounced enrichments in LILE's such as Ba, Sr, Pb.

The redox state of the mantle during and just after core formation.

PubMed

Frost, D J; Mann, U; Asahara, Y; Rubie, D C

2008-11-28

Siderophile elements are depleted in the Earth's mantle, relative to chondritic meteorites, as a result of equilibration with core-forming Fe-rich metal. Measurements of metal-silicate partition coefficients show that mantle depletions of slightly siderophile elements (e.g. Cr, V) must have occurred at more reducing conditions than those inferred from the current mantle FeO content. This implies that the oxidation state (i.e. FeO content) of the mantle increased with time as accretion proceeded. The oxygen fugacity of the present-day upper mantle is several orders of magnitude higher than the level imposed by equilibrium with core-forming Fe metal. This results from an increase in the Fe2O3 content of the mantle that probably occurred in the first 1Ga of the Earth's history. Here we explore fractionation mechanisms that could have caused mantle FeO and Fe2O3 contents to increase while the oxidation state of accreting material remained constant (homogeneous accretion). Using measured metal-silicate partition coefficients for O and Si, we have modelled core-mantle equilibration in a magma ocean that became progressively deeper as accretion proceeded. The model indicates that the mantle would have become gradually oxidized as a result of Si entering the core. However, the increase in mantle FeO content and oxygen fugacity is limited by the fact that O also partitions into the core at high temperatures, which lowers the FeO content of the mantle. (Mg,Fe)(Al,Si)O3 perovskite, the dominant lower mantle mineral, has a strong affinity for Fe2O3 even in the presence of metallic Fe. As the upper mantle would have been poor in Fe2O3 during core formation, FeO would have disproportionated to produce Fe2O3 (in perovskite) and Fe metal. Loss of some disproportionated Fe metal to the core would have enriched the remaining mantle in Fe2O3 and, if the entire mantle was then homogenized, the oxygen fugacity of the upper mantle would have been raised to its present-day level.

Hemispheric dichotomy in lithosphere growth on Mars caused by differences in crustal composition

NASA Astrophysics Data System (ADS)

Thiriet, M.; Michaut, C.; Breuer, D.

2016-12-01

The surface dichotomy is the most striking feature of Mars. The Northern hemisphere is covered by extensive lava plains and is lower in altitude than the South which has higher and sharper reliefs and is more craterized and older than the North. Recent studies have suggested that this bimodal distribution of altitudes could be due to the existence of a buried felsic component similar to the terrestrial continental crust in the Southern hemisphere. The presence of a large buried component of evolved composition might imply an enrichment in incompatible radioactive elements. The thermal surface properties of the two hemispheres also seem to differ; the South shows fine-particulate materials probably resulting from explosive volcanism, while the Northern lava flows are more consolidated and characterized by a higher thermal conductivity. Using a parameterized convection model with a stagnant lid, we computed the thermal evolution and lithosphere growth of Mars accounting for potential differences in the thermal parameters characterizing the Northern and Southern crusts. We find that a stronger enrichment in radioactive elements and a lower surface conductivity in the South can cause a significant difference in elastic thickness of the lithosphere in between both hemispheres, with an elastic lithosphere thicker in the North by several tens of kilometers today. This result might explain the large and still unexplained difference in lithosphere elastic thickness estimated below the two polar caps, which is about 300 km in the North and only 140 km in the South. Assuming a crust in the Northern hemisphere with a thickness of 40 km, a density of 3000 kg/m3 and an enrichment factor in radioactive elements of 5 relative to the primitive mantle, Monte Carlo inversions show that the Southern crust requires a thickness of >60 km, a density between 2700 and 3000 kg/m3 and an enrichment factor of 13-20 to explain such a difference in lithosphere elastic thickness.

Lu-Hf and Sm-Nd evolution in lunar mare basalts

DOE Office of Scientific and Technical Information (OSTI.GOV)

Unruh, D.M.; Stille, P.; Patchett, P.J.

1984-02-15

Lu-Hf and Sm-Nd data for mare basalts combined with Rb-Sr and total REE data taken from the literature suggest that the mare basalts were derived by small (< or =10%) degrees of partial melting of cumulate sources, but that the magma ocean from which these sources formed was light REE and Hf-enriched. Calculated source compositions range fromm lherzolite to olivine websterite. Nonmodal melting of small amounts of ilmenite (< or =3%) in the sources seems to be required by the Lu/Hf data. A comparison of the Hf and Nd isotopic characteristics between the mare basalts and terrestrial oceanic basalts revealsmore » that the epsilonHf/epsilonNd ratios of low-Ti mare basalts are much higher than in terrestrial oceanic basalts. The results are qualitatively consistent with the hypothesis that terrestrial basalt sources are partial melt residues whereas mare basalt sources are cumulates. Alternatively, the results may imply that the terrestrial mantle has evolved in two (or more) stages of evolution, and that the net effect was depletion of the mantle during the first approx.1-3 b.y. followed by enrichment during the last 1-2 b.y.; or simply that there is a difference in Lu-Hf crystal-liquid partitioning (relative to Sm-Nd) between the lunar and terrestrial mantles.« less

HSE Abundances in Angrites and HEDs: Core-Mantle Equilibration or Late Accretion Addition of a Chondritic Component

NASA Astrophysics Data System (ADS)

Rai, N.; Downes, H.; Smith, C. L.

2016-08-01

Using metal-silicate partitioning of HSEs together with their mantle abundances in Vesta and the APB respectively, we test whether formation of a metallic core could have led to the observed abundances of the HSEs, in the mantles of these bodies.

Temporal and Spatial Variability in the Geochemistry of Axial and CoAxial Segment Lavas and their Mantle Sources

NASA Astrophysics Data System (ADS)

Smith, M. C.; Perfit, M. R.; Davis, C.; Kamenov, G. D.

2011-12-01

Three spatially related volcanic eruptions along the CoAxial Segment of the Juan de Fuca Ridge (JdFR) have documented emplacements between 1981 and 1993. Two of the historic flows outcrop at the "Flow Site" and were emplaced within less than 12 years and 500 m from one another. The third was emplaced at the "Floc Site" to the south in the 1980s. Previous studies have documented that CoAxial lavas are among the most incompatible element and isotopically depleted lavas along the entire JdFR, whereas the Axial Seamount segment immediately south of CoAxial has erupted the most chemically enriched lavas south of the Endeavor Segment. Geochemical studies have shown little temporal change in the chemistry of recent Axial Seamount eruptives, whereas CoAxial lavas exhibit distinct chemical differences over short time periods. Significant chemical differences observed among depleted CoAxial lavas emplaced close to one another in space and time are in marked contrast to the relatively constant chemical characteristics of enriched lavas erupted at the magmatically more robust Axial segment only 10's of kilometers to the south and west. New trace element and isotopic (Sr, Nd, Pb) geochemical analyses of historic and older CoAxial lavas have resulted in better documentation of interflow and intraflow chemical variation providing an improved understanding of spatial/temporal chemical variability in lavas, and further insight into JdFR magmatic processes. Modeling of major and trace element abundances suggest that the observed intraflow chemical variation within CoAxial lavas is largely due to shallow-level fractional crystallization but that a single fractional crystallization model cannot account for all interflow chemical variation. In fact, elemental and isotopic data require different parental magmas for each of the three recent CoAxial Segment lava flows suggesting very short-term differences or changes in the chemical character of the mantle source region. In particular, the 1980's Flow Site parental magma may have formed at higher pressures and due to smaller extents of melting than those magmas that erupted just over a decade later. A comparative analysis of the chemistry of CoAxial segment lavas with that of lavas from nearby seamounts, including Axial Seamount, and ridge segments show that much (though not all) of the data conforms well to binary mixing arrays, suggesting that many of the parental lavas from this region of the JdFR can be formed from variable amounts of mixing of two or more distinct mantle end-member sources. In addition to one or more depleted mantle (DM) sources, regional isotopic data also likely suggest a high U/Pb (HIMU) source component within the region of mantle melt generation. For most lavas strong correlations exist between long-lived radiogenic isotopes and ratios of the abundances of highly incompatible elements, suggesting that mantle heterogeneities sampled are ancient, however, in some cases elemental data is decoupled from the radiogenic isotope data indicating more recent depletion events.

Isotopic constraints on the genesis and evolution of basanitic lavas at Haleakala, Island of Maui, Hawaii

USGS Publications Warehouse

Phillips, Erin H.; Sims, K.W.W.; Sherrod, David R.; Salters, Vincent; Blusztajn, Jurek; Dulaiova, Henrieta

2016-01-01

To understand the dynamics of solid mantle upwelling and melting in the Hawaiian plume, we present new major and trace element data, Nd, Sr, Hf, and Pb isotopic compositions, and 238U–230Th–226Ra and 235U–231Pa–227Ac activities for 13 Haleakala Crater nepheline normative basanites with ages ranging from ∼900 to 4100 yr B.P. These basanites of the Hana Volcanics exhibit an enrichment in incompatible trace elements and a more depleted isotopic signature than similarly aged Hawaiian shield lavas from Kilauea and Mauna Loa. Here we posit that as the Pacific lithosphere beneath the active shield volcanoes moves away from the center of the Hawaiian plume, increased incorporation of an intrinsic depleted component with relatively low 206Pb/204Pb produces the source of the basanites of the Hana Volcanics. Haleakala Crater basanites have average (230Th/238U) of 1.23 (n = 13), average age-corrected (226Ra/230Th) of 1.25 (n = 13), and average (231Pa/235U) of 1.67 (n = 4), significantly higher than Kilauea and Mauna Loa tholeiites. U-series modeling shows that solid mantle upwelling velocity for Haleakala Crater basanites ranges from ∼0.7 to 1.0 cm/yr, compared to ∼10 to 20 cm/yr for tholeiites and ∼1 to 2 cm/yr for alkali basalts. These modeling results indicate that solid mantle upwelling rates and porosity of the melting zone are lower for Hana Volcanics basanites than for shield-stage tholeiites from Kilauea and Mauna Loa and alkali basalts from Hualalai. The melting rate, which is directly proportional to both the solid mantle upwelling rate and the degree of melting, is therefore greatest in the center of the Hawaiian plume and lower on its periphery. Our results indicate that solid mantle upwelling velocity is at least 10 times higher at the center of the plume than at its periphery under Haleakala.

Basanite-nephelinite suite from early Kilauea: Carbonated melts of phlogopite-garnet peridotite at Hawaii's leading magmatic edge

USGS Publications Warehouse

Sisson, T.W.; Kimura, Jun-Ichi; Coombs, M.L.

2009-01-01

A basanite-nephelinite glass suite from early submarine Kilauea defines a continuous compositional array marked by increasing concentrations of incompatible components with decreasing SiO2, MgO, and Al2O3. Like peripheral and post-shield strongly alkalic Hawaiian localities (Clague et al. in J Volcanol Geotherm Res 151:279-307, 2006; Dixon et al. in J Pet 38:911-939, 1997), the early Kilauea basanite-nephelinite glasses are interpreted as olivine fractionation products from primary magnesian alkalic liquids. For early Kilauea, these were saturated with a garnet-phlogopite-sulfide peridotite assemblage, with elevated dissolved CO2 contents responsible for the liquids' distinctly low-SiO2 concentrations. Reconstructed primitive liquids for early Kilauea and other Hawaiian strongly alkalic localities are similar to experimental 3 GPa low-degree melts of moderately carbonated garnet lherzolite, and estimated parent magma temperatures of 1,350-1,400??C (olivine-liquid geothermometry) match the ambient upper mantle geotherm shortly beneath the base of the lithosphere. The ???3 GPa source regions were too hot for stable crystalline carbonate and may have consisted of ambient upper mantle peridotite containing interstitial carbonate-silicate or carbonatitic liquid, possibly (Dixon et al. in Geochem Geophys Geosyst 9(9):Q09005, 2008), although not necessarily, from the Hawaiian mantle plume. Carbonate-enriched domains were particularly susceptible to further melting upon modest decompression during upward lithospheric flexure beneath the advancing Hawaiian Arch, or by conductive heating or upward drag by the Hawaiian mantle plume. The early Kilauea basanite-nephelinite suite has a HIMU-influenced isotopic character unlike other Hawaiian magmas (Shimizu et al. in EOS Tran Amer Geophys Union 82(47): abstr V12B-0962, 2001; Shimizu et al. in Geochim Cosmochim Acta 66(15A):710, 2002) but consistent with oceanic carbonatite involvement (Hoernle et al. in Contrib Mineral Petrol 142:520-542, 2002). It may represent the melting products of a fertile domain in the ambient upper mantle impinged upon and perturbed by the sustained plume source that feeds later shield-stage magmatism. ?? US Government 2009.

Influence of precipitating light elements on stable stratification below the core/mantle boundary

NASA Astrophysics Data System (ADS)

O'Rourke, J. G.; Stevenson, D. J.

2017-12-01

Stable stratification below the core/mantle boundary is often invoked to explain anomalously low seismic velocities in this region. Diffusion of light elements like oxygen or, more slowly, silicon could create a stabilizing chemical gradient in the outermost core. Heat flow less than that conducted along the adiabatic gradient may also produce thermal stratification. However, reconciling either origin with the apparent longevity (>3.45 billion years) of Earth's magnetic field remains difficult. Sub-isentropic heat flow would not drive a dynamo by thermal convection before the nucleation of the inner core, which likely occurred less than one billion years ago and did not instantly change the heat flow. Moreover, an oxygen-enriched layer below the core/mantle boundary—the source of thermal buoyancy—could establish double-diffusive convection where motion in the bulk fluid is suppressed below a slowly advancing interface. Here we present new models that explain both stable stratification and a long-lived dynamo by considering ongoing precipitation of magnesium oxide and/or silicon dioxide from the core. Lithophile elements may partition into iron alloys under extreme pressure and temperature during Earth's formation, especially after giant impacts. Modest core/mantle heat flow then drives compositional convection—regardless of thermal conductivity—since their solubility is strongly temperature-dependent. Our models begin with bulk abundances for the mantle and core determined by the redox conditions during accretion. We then track equilibration between the core and a primordial basal magma ocean followed by downward diffusion of light elements. Precipitation begins at a depth that is most sensitive to temperature and oxygen abundance and then creates feedbacks with the radial thermal and chemical profiles. Successful models feature a stable layer with low seismic velocity (which mandates multi-component evolution since a single light element typically increases seismic velocity) growing to its present-day size while allowing enough precipitation to drive compositional convection below. Crucially, this modeling offers unique constrains on Earth's accretion and the light element composition of the core compared to degenerate estimates derived from bulk density and seismic measurements.

An Equation Governing Ultralow-Velocity Zones: Implications for Holes in the ULVZ, Lateral Chemical Reactions at the Core-Mantle Boundary, and Damping of Heat Flux Variations in the Core

NASA Astrophysics Data System (ADS)

Hernlund, J. W.; Matsui, H.

2017-12-01

Ultralow-velocity zones (ULVZ) are increasingly illuminated by seismology, revealing surprising diversity in size, shape, and physical characteristics. The only viable hypotheses are that ULVZs are a compositionally distinct FeO-enriched dense material, which could have formed by fractional crystallization of a basal magma ocean, segregation of subducted banded iron formations, precipitation of solids from the outer core, partial melting and segregation of iron-rich melts from subducted basalts, or most likely a combination of many different processes. But many questions remain: Are ULVZ partially molten in some places, and not in others? Are ULVZ simply the thicker portions of an otherwise global thin layer, covering the entire CMB and thus blocking or moderating chemical interactions between the core and overlying mantle? Is such a layer inter-connected and able to conduct electrical currents that allow electro-magnetic coupling of core and mantle angular momentum? Are they being eroded and shrinking in size due to viscous entrainment, or is more material being added to ULVZ over time? Here we derive an advection-diffusion-like equation that governs the dynamical evolution of a chemically distinct ULVZ. Analysis of this equation shows that ULVZ should become readily swept aside by viscous mantle flows at the CMB, exposing "ordinary mantle" to the top of the core, thus inducing chemical heterogeneity that drives lateral CMB chemical reactions. These reactions are correlated with heat flux, thus maintaining large-scale pressure variations atop the core that induce cyclone-like flows centered around ULVZ and ponded subducted slabs. We suggest that turbulent diffusion across adjacent cyclone streams inside a stratified region atop the core readily accommodates lateral transport and re-distribution of components such as O and Si, in addition to heat. Our model implies that the deeper core is at least partly shielded from the influence of strong heat flux variations at the CMB which might otherwise cause problems for producing a geodynamo.

Slab and Sediment Melting during Subduction Initiation: Mantle Plagiogranites from the Oman Ophiolite

NASA Astrophysics Data System (ADS)

Rollinson, H. R.

2014-12-01

Granitoid dykes up to several hundred metres wide and 2 km long are found in depleted harzburgites in the mantle section of the Oman ophiolite. They vary in composition from tonalite to potassic granite and are generally more potassic than the crustal plagiogranites found within the sheeted dyke complex higher up within the ophiolite stratigraphy. Some granites are strongly peraluminous and contain garnet and andalusite. They are geochemically variable, some with REE that are relatively unfractionated ((La/Yb)n= 3.5-6.0, flat middle to heavy REE, steep light REE) to those which are highly fractionated ((La/Yb)n= 28-220). On primitive-mantle normalised plots some have very high concentrations of fluid-mobile elements - Cs, Rb, Th, U and Pb. Few have significant Ta-Nb anomalies. On the Ca-Fe-Mg-Ti discrimination diagram of Patino Douce (J. Petrol., 1999) whole-rock compositions define a spectrum between felsic-pelite derived melts and amphibolite-derived melts. There is a chemical similarity between the least REE fractionated plagiogranites (generally tonalites and granodiorites) and melts of an amphibolitic parent. This is supported by the occurrence of mafic xenoliths in some dykes, the presence of hornblende and highly calcic cores (up to An85) in some plagioclase grains. Trace element modelling using Oman Geotimes lavas as the starting composition indicates that melting took place in the garnet stability field, although enrichment in the melt in Cs, Rb, Ba and Pb suggests that there was another component present in addition to the mafic parent. Other plagiogranites (trondhjemites and granites) have a strongly peraluminous chemistry and mineralogy and geochemical similarities with the Himalayan leucogranites implying that they were derived from a sedimentary protolith. These mantle plagiogranites are more prevalent in the northern outcrops of the ophiolite. The volume of granitoid melt and the depth of melting preclude their derivation from the sole of the ophiolite, rather they were derived during subduction by the partial melting of the slab and associated sediment and emplaced into the overlying mantle wedge. Current subduction-initiation models for supra-subduction ophiolites should integrate this process into their thinking.

Basanite-nephelinite suite from early Kilauea: carbonated melts of phlogopite-garnet peridotite at Hawaii's leading magmatic edge

NASA Astrophysics Data System (ADS)

Sisson, T. W.; Kimura, J.-I.; Coombs, M. L.

2009-12-01

A basanite-nephelinite glass suite from early submarine Kilauea defines a continuous compositional array marked by increasing concentrations of incompatible components with decreasing SiO2, MgO, and Al2O3. Like peripheral and post-shield strongly alkalic Hawaiian localities (Clague et al. in J Volcanol Geotherm Res 151:279-307, 2006; Dixon et al. in J Pet 38:911-939, 1997), the early Kilauea basanite-nephelinite glasses are interpreted as olivine fractionation products from primary magnesian alkalic liquids. For early Kilauea, these were saturated with a garnet-phlogopite-sulfide peridotite assemblage, with elevated dissolved CO2 contents responsible for the liquids’ distinctly low-SiO2 concentrations. Reconstructed primitive liquids for early Kilauea and other Hawaiian strongly alkalic localities are similar to experimental 3 GPa low-degree melts of moderately carbonated garnet lherzolite, and estimated parent magma temperatures of 1,350-1,400°C (olivine-liquid geothermometry) match the ambient upper mantle geotherm shortly beneath the base of the lithosphere. The ~3 GPa source regions were too hot for stable crystalline carbonate and may have consisted of ambient upper mantle peridotite containing interstitial carbonate-silicate or carbonatitic liquid, possibly (Dixon et al. in Geochem Geophys Geosyst 9(9):Q09005, 2008), although not necessarily, from the Hawaiian mantle plume. Carbonate-enriched domains were particularly susceptible to further melting upon modest decompression during upward lithospheric flexure beneath the advancing Hawaiian Arch, or by conductive heating or upward drag by the Hawaiian mantle plume. The early Kilauea basanite-nephelinite suite has a HIMU-influenced isotopic character unlike other Hawaiian magmas (Shimizu et al. in EOS Tran Amer Geophys Union 82(47): abstr V12B-0962, 2001; Shimizu et al. in Geochim Cosmochim Acta 66(15A):710, 2002) but consistent with oceanic carbonatite involvement (Hoernle et al. in Contrib Mineral Petrol 142:520-542, 2002). It may represent the melting products of a fertile domain in the ambient upper mantle impinged upon and perturbed by the sustained plume source that feeds later shield-stage magmatism.

Geochemistry of Early Paleozoic boninites from the Central Qilian block, Northwest China: Constraints on petrogenesis and back-arc basin development

NASA Astrophysics Data System (ADS)

Gao, Zhong; Zhang, Hong-Fei; Yang, He; Luo, Bi-Ji; Guo, Liang; Xu, Wang-Chun; Pan, Fa-Bin

2018-06-01

Early Paleozoic boninites occur in the Central Qilian orogenic belt, Northwest China. Their petrogenesis provides insights into lithosphere process and tectonic evolution of the Qilian block. In this paper, we carry out a study of geochronological, geochemical and Sr-Nd isotopic compositions for the Early Paleozoic boninites in the Lajishan area of the Central Qilian block. The Lajishan boninites (∼483 Ma) have high Al2O3/TiO2 (36.7-64.7) and CaO/TiO2 (31.1-49.6) ratios, and high MgO (7.86-10.47 wt%), Cr (439-599 ppm) and Ni (104-130 ppm) contents, indicating that the boninites result from a refractory mantle source. They are depleted in high field-strength elements (HFSE) and enriched in large ion lithophile elements (LILE), coupled with slightly high initial 87Sr/86Sr values of 0.7059-0.7074 and low εNd(t) values of -1.05 to +2.66, indicating that the mantle source was metasomatized by subducted slab-derived components. We found that an assemblage of low-Ca group and high-Ca group boninites occurred in the Lajishan belt. The high-Ca group boninites were derived from relatively fertile mantle with slightly higher melting degree, whereas the low-Ca group boninites were generated by partial melting of more refractory mantle wedge peridotites with slightly lower melting degree. The assemblage of low-Ca group and high-Ca group boninites reveals that the low-Ca group boninites were generated by the further melting of the more refractory mantle source after the segregation of the high-Ca group boninitic magmas in response to the back-arc basin opening. In the light of reported boninites worldwide, a diagram of Zr/Y vs. CaO/Al2O3 is used to identify boninites in fore-arc and back-arc regions. We suggest that the Lajishan boninites represent the products of back-arc basin development in response to the northward subduction of the Qaidam-West Qinling ocean slab.

Tectonomagmatic evolution of the Earth and Moon

NASA Astrophysics Data System (ADS)

Sharkov, E. V.; Bogatikov, O. A.

2010-03-01

The Earth and Moon evolved following a similar scenario. The formation of their protocrusts started with upward crystallization of global magmatic oceans. As a result of this process, easily fusible components accumulated in the course of fractional crystallization of melt migrating toward the surface. The protocrusts (granitic in the Earth and anorthositic in the Moon) are retained in ancient continents. The tectonomagmatic activity at the early stage of planet evolution was related to the ascent of mantle plume of the first generation composed of mantle material depleted due to the formation of protocrusts. The regions of extension, rise, and denudation were formed in the Earth above the diffluent heads of such superplumes (Archean granite-greenstone domains and Paleoproterozoic cratons), whereas granulite belts as regions of compression, subsidence, and sedimentation arose above descending mantle flows. The situation may be described in terms of plume tectonics. Gentle uplifts and basins ( thalassoids) in lunar continents are probable analogues of these structural elements in the Moon. The period of 2.3-2.0 Ga ago was a turning point in the tectonomagmatic evolution of the Earth, when geochemically enriched Fe-Ti picrites and basalts typical of Phanerozoic within-plate magmatism became widespread. The environmental setting on the Earth’s surface changed at that time, as well. Plate tectonics, currently operating on a global scale, started to develop about ˜2 Ga ago. This turn was related to the origination of thermochemical mantle plumes of the second generation at the interface of the liquid Fe-Ni core and silicate mantle. A similar turning point in the lunar evolution probably occurred 4.2-3.9 Ga ago and completed with the formation of large depressions ( seas) with thinned crust and vigorous basaltic magmatism. Such a sequence of events suggests that qualitatively new material previously retained in the planets’ cores was involved in tectonomagmatic processes at the middle stage of planetary evolution. This implies that the considered bodies initially were heterogeneous and were then heated from above to the bottom by propagation of a thermal wave accompanied by cooling of outer shells. Going through the depleted mantle, this wave generated thermal superplumes of the first generation. Cores close to the Fe + FeS eutectics in composition were affected by this wave in the last turn. The melting of the cores resulted in the appearance of thermochemical superplumes and corresponding irreversible rearrangement of geotectonic processes.

The Xenon record of Earth's early differentiaiton

NASA Astrophysics Data System (ADS)

Peto, M. K.; Mukhopadhyay, S.; Kelley, K. A.

2011-12-01

Xenon isotopes in mantle derived rocks provide information on the early differentiation of the silicate mantle of our planet. {131,132 134,136}Xe isotopes are produced by the spontaneous fission of two different elements: the now extinct radionuclide 244Pu, and the long-lived 238U. These two parent nuclides, however, yield rather different proportion of fissiogenic Xenon isotopes. Hence, the proportion of Pu- to U-derived fission xenon is indicative of the degree and rate of outgassing of a mantle reservoir. Recent data obtained from Iceland in our lab confirm that the Xenon isotopic composition of the plume source(s) is characterized by lower 136Xe/130Xe ratios than the MORB source and the Iceland plume is more enriched in the Pu-derived Xenon component. These features are interpreted as reflecting different degrees of outgassing and appear not to be the result of preferential recycling of Xenon to the deep mantle. To further investigate how representative the Icelandic measurements might be of other mantle plumes, we measured noble gases (He, Ne, Ar, Xe) in gas-rich basalt glasses from the Rochambeau Ridge (RR) in the Northern Lau Basin. Recent work suggests the presence of a "Samoan-like" OIB source in the northern Lau Basin and our measurements were performed on samples with plume-like 3He/4He ratios (15-28 RA) [1]. The Xenon isotopic measurements indicate that the maximum measured 136Xe/130Xe ratios in the Rochambeau samples are similar to Iceland. In particular, for one of the gas rich samples we were able to obtain 77 different isotopic measurements through step-crushing. Preliminary investigation of this sample suggests higher Pu- to U-derived fission Xenon than in MORBs. To quantitatively evaluate the degree and rate of outgassing of the plume and MORB reservoirs, particularly during the first few hundred million years of Earth's history, we have modified a geochemical reservoir model that was previously developed to investigate mantle overturn and mixing from He, Ar and lithophile isotopes [2]. We will present the results from this geochemical reservoirs model, which is constrained by our high precision dataset from the Rochambeau Rift (Northern Lau Basin) and Iceland along with the Xenon dataset from popping rock [3]. [1] Lupton et al., GRL, 2009. [2] Gonnermann and Mukhopadhyay, Nature, 2009. [3] Kunz et al., Science, 1998.

Istopically Defined Source Reservoirs of Primitive Magmas in the East African Rift.

NASA Astrophysics Data System (ADS)

Rooney, T. O.; Furman, T.; Hanan, B.

2005-12-01

Extension within the East African Rift is a function of the interaction between plume-driven uplift and far-field stresses associated with plate tectonic processes. Geochemical and isotopic investigation of primitive basalts from the Main Ethiopian Rift (MER) reveals systematic spatial variations in the contributions from distinct and identifiable source reservoirs that, in turn help identify the mechanisms by which along-axis rifting has progressed. The Sr-Nd-Pb isotopic characteristics of MER basalts can be described by a three-component mixing model involving the long-lived Afar plume, a depleted mantle component similar to the source region for Gulf of Aden MORB from east of 48° E and a reservoir that is likely lithospheric (sub-continental mantle lithosphere, magmatic underplate or lower crust). Quaternary basalts in the central MER exhibit a systematic decrease in plume influence southward from 9.5° N to 8° N, i.e., away from the modern surface expression of the Afar plume in Djibouti and Erta 'Ale. The composition of the Afar plume component is comparable to the "C" mantle reservoir. This southward decrease in plume influence is coupled with an increase in the influence of the lithospheric and depleted mantle components. Linear arrays observed within Pb-Pb isotopic space at each eruptive center require distinctive ratio of lithospheric + depleted mantle components mixing with variable amounts of the "C"-like plume component. This isotopic evidence suggests the depleted mantle and lithosphere mixed prior to the generation of the recent magmas. To the south, the Sr-Nd-Pb isotopic compositions of Turkana (Kenya) rift basalts record a mix of a similar "C"-like plume component and a fourth HIMU-like source component. Low 3He/4He values observed in the HIMU-dominated lavas from Turkana contrast with the higher ratios found in basalts associated with the "C"-like Afar plume. Further analysis of "C"-HIMU lavas at Turkana is required to fully constrain the He isotopic signatures. Thus, along-axis patterns in Quaternary EARS magmatism are compatible with two "C"-like plumes with contributions from the upper mantle and chemically distinct lithospheric components. Alternatively, a single "C"-like plume can account for these relationships. In the single plume scenario, the HIMU source component present in the 30 Ma Turkana lavas may represent melting of metasomatised lithosphere, derived from the accretion of island-arc-backarc basins during Pan-African events (e.g. Schilling et al., 1992). The recent plume-dominated activity in Turkana and Afar are separated by a region characterized by waning plume influence and a greater contribution from the depleted mantle. This intermediate zone, which is located in the south-central MER represents the modern site of contact between the northward propagating Kenya / Turkana Rift and the southward propagating Afar Rift zone.

Density-Pressure Profiles of Fe-Bearing MgSiO3 Liquid: Effects of Valence and Spin States, and Implications for the Chemical Evolution of the Lower Mantle

NASA Astrophysics Data System (ADS)

Karki, Bijaya B.; Ghosh, Dipta B.; Maharjan, Charitra; Karato, Shun-ichiro; Park, Jeffrey

2018-05-01

Density is a key property controlling the chemical state of Earth's interior. Our knowledge about the density of relevant melt compositions is currently poor at deep-mantle conditions. Here we report results from first-principles molecular-dynamics simulations of Fe-bearing MgSiO3 liquids considering different valence and spin states of iron over the whole mantle pressure conditions. Our simulations predict the high-spin to low-spin transition in both ferrous and ferric iron in the silicate liquid to occur gradually at pressures around 100 GPa. The calculated iron-induced changes in the melt density (about 8% increase for 25% iron content) are primarily due to the difference in atomic mass between Mg and Fe, with smaller contributions (<2%) from the valence and spin states. A comparison of the predicted density of mixtures of (Mg,Fe)(Si,Fe)O3 and (Mg,Fe)O liquids with the mantle density indicates that the density contrast between the melt and residual-solid depends strongly on pressure (depth): in the shallow lower mantle (depths < 1,000 km), the melt is lighter than the solids, whereas in the deep lower mantle (e.g., the D″ layer), the melt density exceeds the mantle density when iron content is relatively high and/or melt is enriched with Fe-rich ferropericlase.

Assimilation of sediments embedded in the oceanic arc crust: myth or reality?

NASA Astrophysics Data System (ADS)

Bezard, Rachel; Davidson, Jon P.; Turner, Simon; Macpherson, Colin G.; Lindsay, Jan M.; Boyce, Adrian J.

2014-06-01

Arc magmas are commonly assumed to form by melting of sub-arc mantle that has been variably enriched by a component from the subducted slab. Although most magmas that reach the surface are not primitive, the impact of assimilation of the arc crust is often ignored with the consequence that trace element and isotopic compositions are commonly attributed only to varying contributions from different components present in the mantle. This jeopardises the integrity of mass balance recycling calculations. Here we use Sr and O isotope data in minerals from a suite of volcanic rocks from St Lucia, Lesser Antilles arc, to show that assimilation of oceanic arc basement can be significant. Analysis of 87Sr/86Sr in single plagioclase phenocrysts from four Soufrière Volcanic Complex (SVC; St Lucia) hand samples with similar composition (87Sr/86Sr = 0.7089-0.7091) reveals crystal isotopic heterogeneity among hand samples ranging from 0.7083 to 0.7094 with up to 0.0008 difference within a single hand sample. δO18 measurements in the SVC crystals show extreme variation beyond the mantle range with +7.5 to +11.1‰ for plagioclase (n=19), +10.6 to +11.8‰ for quartz (n=10), +9.4 to +9.8‰ for amphibole (n=2) and +9 to +9.5‰ for pyroxene (n=3) while older lavas (Pre-Soufriere Volcanic Complex), with less radiogenic whole rock Sr composition (87Sr/86Sr = 0.7041-0.7062) display values closer to mantle range: +6.4 to +7.9‰ for plagioclase (n=4) and +6 to +6.8‰ for pyroxene (n=5). We argue that the 87Sr/86Sr isotope disequilibrium and extreme δO18 values provide compelling evidence for assimilation of material located within the arc crust. Positive correlations between mineral δO18 and whole rock 87Sr/86Sr, 143Nd/144Nd and 206,207,208Pb/204Pb shows that assimilation seems to be responsible not only for the isotopic heterogeneity observed in St Lucia but also in the whole Lesser Antilles since St Lucia encompasses almost the whole-arc range of isotopic compositions. This highlights the need for detailed mineral-scale investigation of oceanic arc suites to quantify assimilation that could otherwise lead to misinterpretation of source composition and subduction processes.

Os, Nd and Sr isotope and trace element geochemistry of the Muli picrites: Insights into the mantle source of the Emeishan Large Igneous Province

NASA Astrophysics Data System (ADS)

Li, Jie; Xu, Ji-Feng; Suzuki, Katsuhiko; He, Bin; Xu, Yi-Gang; Ren, Zhong-Yuan

2010-09-01

A suite of picrites and basalts from the Muli area, in the northwestern part of the Emeishan continental flood basalt province, provides new and valuable information on the geochemistry of the Emeishan Large Igneous Province (LIP) and its source. The Muli picrites can be classified as type-1 or type-2. The former shows ocean-island basalt-like trace element characteristics, with γ Os (260 Ma) values and ɛ Nd (260 Ma) values ranging from + 7.5 to + 11.5 and from + 6.0 to + 7.8, respectively. This is the first time that picrites with highly radiogenic Os and high Os contents (up to 3.3 ppb) have been recognized in the Emeishan LIP. These characteristics probably reflect a relatively enriched component in the Emeishan LIP source. The type-2 picrites are characterized by non-radiogenic γ Os (260 Ma) values ranging from - 4.2 to - 0.3, and they may be further subdivided into type-2A and type-2B picrites. Type-2A picrites contain moderate amounts of the light rare earth elements (LREEs), have low Ce N/Yb N values (1.1-2.0), and a relatively high initial ɛ Nd (+ 5.0 to + 6.6). In terms of Os and Nd isotopes, the Muli type-2A picrites are similar to the Song Da komatiites of Vietnam and the Gorgona Island picrites, revealing the existence of a depleted mantle component in the Emeishan LIP source. In contrast with the type-2A picrites, type-2B lavas exhibit a negative Nb anomaly and relatively lower initial ɛ Nd and γ Os values (Nb/La > 1.8; ɛ Nd (260 Ma) = - 5.5 to + 6.4; γ Os (260 Ma) = - 4.2 to - 1.9), suggesting that the type-2B lavas have a depleted mantle source, similar to type-2A, but that the type-2B lavas are also influenced by various degrees of mixing of depleted plume-derived melt, sub-continental lithospheric mantle, and/or continental crust. Given that the basalts in the Muli area show similar geochemical features to those of the type-2B picrites, their origins are inferred to be similar.

Highly Sideophile Element Abundance Constraints on the Nature of the Late Accretionary Histories of Earth, Moon and Mars

NASA Technical Reports Server (NTRS)

Walker, R. J.; Puchtel, I. S.; Brandon, A. D.; Horan, M. F.; James, O. B.

2007-01-01

The highly siderophile elements (HSE) include Re, Os, Ir, Ru, Pt and Pd. These elements are initially nearly-quantitatively stripped from planetary silicate mantles during core segregation. They then may be re-enriched in mantles via continued accretion sans continued core segregation. This suite of elements and its included long-lived radiogenic isotopes systems (Re-187 (right arrow) Os-187; Pt-190 (right arrow) Os-186) can potentially be used to fingerprint the characteristics of late accreted materials. The fingerprints may ultimately be useful to constrain the prior nebular history of the dominant late accreted materials, and to compare the proportion and genesis of late accretionary materials added to the inner planets. The past ten years have seen considerable accumulation of isotopic and compositional data for HSE present in the Earth's mantle, lunar mantle and impact melt breccias, and Martian meteorites. Here we review some of these data and consider the broader implications of the compiled data.

Secondary overprinting of S-Se-Te signatures in the Earth's mantle: Implications for the Late Veneer

NASA Astrophysics Data System (ADS)

Koenig, S.; Luguet, A.; Lorand, J.; Pearson, D.

2013-12-01

Sulphur, Selenium and Tellurium are both chalcophile and highly siderophile elements (HSE) with near-chondritic ratios and absolute abundances in the terrestrial mantle that exceed those predicted by core-mantle differentiation[1]. These 'excess' HSE abundances have been attributed to addition of ca. 0.5% of chondrite-like material that hit the Earth in its accretionary stage between 4 to 3.8 billion years ago after core-mantle differentiation (Late Veneer[2]). Therefore, like other HSE, S, Se and Te are considered potential tracers for the composition of the Late Veneer, provided that their bulk silicate Earth abundances are properly constrained. In contrast to ca. 250 ppm S, Se and Te are ultra-trace elements in the terrestrial mantle. Like all HSE, they are furthermore controlled by base metal sulphides (BMS) and micrometric platinum group minerals (PGMs)[3]. This strong control exerted by the host mineralogy and petrology on the S-Se-Te systematics at both the micro-scale and the whole-rock scale makes detailed mineralogical and petrological studies of BMS and PGM a pre-requisite to fully understand and accurately interpret the whole-rock signatures. Here we combine in-situ sulphide data and detailed mineralogical observations with whole-rock S-Se-Te-HSE signatures of both lherzolites and harburgites from different geodynamic settings. We demonstrate that the near-chondritic Se and Te signature of 'fertile' mantle rocks (Se/Te ≈9×5) is not a primitive signature of the Earth's mantle, but rather reflects strong enrichment in metasomatic HSE host phases, which erased previous pristine signatures. Consequently, current attempts to identify a potential Late Veneer composition are seriously flawed because, neither refertilisation/metasomatism nor true melt depletion (e.g. harzburgitic residues) have been taken into account for the Primitive Upper Mantle composition estimate[4]. Our combined whole rock and in-situ sulphide data indicate a refertilisation trend towards sub-chondritic Se/Te ratios (i.e. Se/Te < 2). On the other hand, harzburgites that preserve depletion signatures show suprachondritic Se/Te ratios (< 31). Altogether this shows that metasomatic enrichment of mantle rocks may lead to a systematic bias and hence underestimation of the current Se/Te estimate of the primitive mantle. The metasomatic origin of the reported S, Se and Te ratios in peridotites that reflect the control of metasomatic BMS and PGMs[5;6] furthermore show that not all whole rock signatures in the Earth's mantle that scatter around near-chondritic values are primary and hence challenge the simple conception that these features may readily solve the long-standing conundrum of the Late Veneer composition. Refs: [1] Rose-Weston et al. (2009) GCA 73, 4598-4615; [2] Kimura et al. (1974) GCA 38, 683-701; [3] Lorand and Alard (2010) 67, 4137-4151; [4] Wang and Becker (2013) Nature 499, 328-331; [5] König et al. (2012) GCA 86, 354-366; [6] König et al. (2013, in press), EPSL.

Compositional diversity of Late Cenozoic basalts in a transect across the southern Washington Cascades: Implications for subduction zone magmatism

NASA Astrophysics Data System (ADS)

Leeman, William P.; Smith, Diane R.; Hildreth, Wes; Palacz, Zen; Rogers, Nick

1990-11-01

Major volcanoes of the Southern Washington Cascades (SWC) include the large Quaternary stratovolcanoes of Mount St. Helens (MSH) and Mount Adams (MA) and the Indian Heaven (IH) and Simcoe Mountain (SIM) volcanic fields. There are significant differences among these volcanic centers in terms of their composition and evolutionary history. The stratovolcanoes consist largely of andesitic to dacitic lavas and pyroclastics with minor basalt flows. IH consists dominantly of basaltic with minor andesite lavas, all erupted from monogenetic rift and cinder cone vents. SIM has a poorly exposed andesite to rhyolite core but mainly consists of basaltic lavas erupted from numerous widely dispersed vents; it has the morphology of a shield volcano. Distribution of mafic lavas across the SWC is related to north-northwest trending faults and fissure zones that indicate a significant component of east-west extension within the area. There is overlap in eruptive history for the areas studied, but it appears that peak activity was progressively older (MSH (<40 Ka), IH (mostly <0.5 Ma), MA (<0.5 Ma), SIM (1-4 Ma)) and more alkalic toward the east. A variety of compositionally distinct mafic magma types has been identified in the SWC, including low large ion lithophile element (LILE) tholeiitic basalts, moderate LILE calcalkalic basalts, basalts transitional between these two, LILE-enriched mildly alkalic basalts, and basaltic andesites. Compositional diversity among basaltic lavas, both within individual centers as well as across the arc, is an important characteristic of the SWC traverse. The fact that the basaltic magmas either show no correlation between isotopic and trace element components or show trends quite distinct from those of the associated evolved lavas, suggests that their compositional variability is attributable to subcrustal processes. Both the primitive nature of the erupted basalts and the fact that they are relatively common in the SWC sector also imply that such magmas had little residence time in the crust. A majority of the SWC basaltic samples studies are indistinguishable from oceanic island basalts (OIB) in terms of trace element and isotopic compositions, and more importantly, most do not display the typical high field strength element (HFSE) depletion seen in subduction-related magmas in volcanic arcs elsewhere. LILE enrichment and HRSE depletion characteristics of most arc magmas are generally attributed to the role of fluids released by dehydration of subducted oceanic lithosphere and to the effects of sediment subduction. Because most SWC basalts lack these compositional features, we conclude that subducted fluids and sediments do not play an essential role in producing these magmas. Rather, we infer that they formed by variable degree melting of a mixed mantle source consisting mainly of heterogeneously distributed OIB and mid-ocean ridge basalt source domains. Relatively minor occurrences of HFSE-depleted arclike basalts may reflect the presence of a small proportion of slab-metasomatized subarc mantle. The juxtaposition of such different mantle domains within the lithospheric mantle is viewed as a consequence of (1) tectonic mixing associated with accretion of oceanic and island arc terranes along the Pacific margin of North America prior to Neogene time, and possibly (2) a seaward jump in the locus of subduction at about 40 Ma. The Cascades arc is unusual in that the subducting oceanic plate is very young and hot. We suggest that slab dehydration outboard of the volcanic front resulted in a diminished role of aqueous fluids in generating or subsequently modifying SWC magmas compared to the situation at most convergent margins. Furthermore, with low fluid flux conditions, basalt generation is presumably triggered by other processes that increase the temperature of the mantle wedge (e.g., convective mantle flow, shear heating, etc.).

Volatiles in melt inclusions from Icelandic magmas

NASA Astrophysics Data System (ADS)

Nichols, A. R.; Wysoczanski, R. J.; Carroll, M. R.

2006-12-01

Melt inclusions hosted in olivine crystals from the glassy rims of subglacially erupted pillow basalts on Iceland have been analysed for volatiles, major elements and trace elements. Volatile measurements were undertaken using Fourier-Transform InfraRed spectroscopy utilising a novel technique which enables unexposed and much smaller inclusions than were previously possible to be analysed. Major elements were measured using electron microprobe and trace elements by laser ablation-inductively coupled plasma-mass spectrometry. Comparison between initial results from the inclusions and the compositions of the bulk glasses show that the inclusions are less evolved and contain more H2O at the same MgO content. In addition many of the inclusions have higher H2O/K2O than their bulk glasses and some even contain CO2 (up to 629 ppm), which is below detection limits in the bulk glasses. This indicates that these inclusions are less affected by degassing. Two inclusions have extreme H2O/K2O (> 10), possibly suggesting that they have assimilated hydrous crustal material. The volatile and major element compositions of the bulk glasses have been used to suggest that the Iceland mantle plume is wet. However, trace element measurements show that enriched Iceland magmas have lower H2O/Ce than the adjacent Reykjanes Ridge. This could reflect syn-eruptive degassing or mixing between undegassed and recycled degassed magmas. Alternatively Iceland magmas could be derived from the EM (enriched mantle) component, which is believed to represent recycled oceanic crust. It is suggested that this material is efficiently dehydrated during the subduction process, so even though it has an enriched character, H2O is relatively depleted. As a result, EM melts have higher absolute H2O contents than mid- ocean ridge basalts (MORB), but lower H2O/Ce (or other H2O-incompatible element ratios), which has led to EM plumes being termed `dampspots'. The inclusion data will be presented in this context. Their compositions will show how the melt has evolved, enabling the relative roles of degassing, crystallisation and assimilation in the volatile systematics to be examined.

Seismic Observations of the Mid-Pacific Large Low Shear Velocity Province

NASA Astrophysics Data System (ADS)

Chan, A.; Helmberger, D. V.; Sun, D.; Li, D.; Jackson, J. M.

2015-12-01

Seismic data from earthquakes originating in the Fiji-Tonga region exhibits waveform complexity of a number of phases which may be attributed to various structures along ray paths to stations of USArray, including anomalous structures at the core-mantle boundary. The data shows variation in multipathing, that is, the presence of secondary arrivals following the S phase at diffracted distances (Sdiff) which suggests that the waveform complexity is due to structures at the eastern edge of the mid-Pacific Large Low Shear Velocity Province (LLSVP). This study examines data from earthquake events while the Transportable Array portion of USArray was situated in the midwest United States, reinforcing previous studies that indicate late arrivals occurring as long as 26 seconds after the primary arrivals (To et al., 2011). Using earth flattening transformations and finite difference methods, simulations of tapered wedge structures of low velocity material allow for wave energy trapping, producing the observed waveform complexity and delayed arrivals at large distances, with such structures having characteristic properties of, for example, a height of 70 km, in-plane extent more than 1000 km, and shear wave velocity drop of 3% at the top to 15% at the bottom relative to PREM. Differential arrival times for SH and SV components suggest anisotropy and possible wave propagation through downgoing slabs beneath the source region. The arrivals of the SPdKS phase further support the presence of an ultra-low velocity zone (ULVZ) within a two-humped LLSVP. Some systematic delays in arrival times of multiple phases for distances less than 102º are accounted for and attributed to the presence of a mantle slab underneath the continental United States. Comparisons to seismic data from earthquakes originating from other locations further constrain depths of the deep mantle structures. Possible explanations include iron-enrichment of deep mantle phases.

Mantle xenoliths hosted in alkali basalts in subduction environment: the example of the SE Alps (Italy)

NASA Astrophysics Data System (ADS)

Gasperini, D.; Maffei, K.; Bosch, D.; Braga, R.; Macera, P.; Morten, L.

2003-04-01

We present petrographic, geochemical, and isotopic (Sr, Nd, and Pb) data of a representative suite of spl-peridotite xenoliths (mg# >88) hosted in alkali basalts from numerous outcrops in the Tertiary Veneto Volcanic Province (VVP; SE Alps, Italy), compared to various world-wide mafic inclusions (French Massif, Australia, China, Philippines, Russia, Kerguelen). The VVP spl-harzburgites and -lherzolites carry textures ranging from protogranular, porphyroclastic, granuloblastic to pyrometamorfic. These samples are characterized by a continuous depletion trend from the cpx-rich lherzolites to harzburgites, with CaO, Al_2O_3, TiO_2, and Na_2O contents decreasing with mg# increasing (Morten, 1987; Beccaluva et al., 2001). Then, the VVP xenoliths spinels show a strong Cr/(Cr+Al) ratio increase at a slight Mg/(Mg+Fe2+) ratio decrease, thus reflecting a variably depleted mantle source. The VVP xenoliths display a large range of enrichment in LREE, K, Rb, Sr and P, suggesting post depletion metasomatic episodes (Morten et al., 2002). Whereas most of the VVP xenoliths' multi-element spectra, incompatible element and isotope ratios are similar to the VVP host basalts, thus with a strong HIMU signature (Macera et al. submitted), some depleted samples show geochemical features typical of crust derived material. These characteristics cannot be related to significant interaction with the local lower continental crust, as represented by several analyzed gabbroic xenoliths. Nevertheless negative Nb and Ta anomalies in analogous peridotitic samples have been previously ascribed to metasomatism inferred by plume rising material in the upper mantle (Bedini et al., 1997). Comparing the VVP peridotites with several mafic xenoliths from various geodynamical environments, we suggest that this crust affinity could be alternatively explained by the presence of a not perfectly homogenized upper crustal component in the source region, probably induced by subduction related episode(s). In this contest, the isotopic composition of the VVP mafic xenoliths is a crucial tool to understand the geochemical history of the Alpine subcontinental mantle.

High-Mg subduction-related Tertiary basalts in Sardinia, Italy

NASA Astrophysics Data System (ADS)

Morra, V.; Secchi, F. A. G.; Melluso, L.; Franciosi, L.

1997-03-01

The Oligo-Miocene volcanics (32-15 Ma), which occur in the Oligo-Miocene Sardinian Rift, were interpreted in the literature as an intracontinental volcanic arc built upon continental crust about 30 km thick. They are characterized by a close field association of dominantly andesites and acid ignimbrites, with subordinate basalts. In this paper we deal with the origin and evolution of recently discovered high-magnesia basalts aged ca. 18 Ma occurring in the Montresta area, northern Sardinia, relevant to the petrogenesis of the Cenozoic volcanics of Sardinia. The igneous rocks of the Montresta area form a tholeiitic, subduction-related suite. Major-element variation from the high-magnesia basalts (HMB) to high-alumina basalts (HAB) are consistent with crystal/liquid fractionation dominated by olivine and clinopyroxene. Proportions of plagioclase and titanomagnetite increase from HAB to andesites. Initial {87Sr }/{86Sr } ratios increase with differentiation from 0.70398 for the HMB to 0.70592 for the andesites. This suggests concomitant crustal contamination. The geochemical characteristics of the high-magnesia basalts are typical of subduction-related magmas, with negative Nb, Zr and Ti spikes in mantle-normalized diagrams. It is proposed that these high-magnesia basalts were produced by partial melting of a mantle source characterized by large-ion lithophile elements (LILE) enrichment related principally to dehydration of subducted oceanic crust. Chondrite-normalized rare earth elements (REE) patterns indicate that the lavas are somewhat enriched in light rare earth elements (LREE), with flat heavy rare earth elements (HREE) patterns. This evidence is consistent with a spinel-bearing mantle source. The sub-parallel chondrite-normalized patterns show enrichment with differentiation, with a greater increase of LREE than HREE. The occurrence of high-magnesia basalts at 18 Ma in Sardinia appears to be correlated with and favoured by pronounced extensional tectonics at that time.

On the development of the calc-alkaline and tholeiitic magma series: A deep crustal cumulate perspective

NASA Astrophysics Data System (ADS)

Chin, Emily J.; Shimizu, Kei; Bybee, Grant M.; Erdman, Monica E.

2018-01-01

Two distinct igneous differentiation trends - the tholeiitic and calc-alkaline - give rise to Earth's oceanic and continental crust, respectively. Mantle melting at mid-ocean ridges produces dry magmas that differentiate at low-pressure conditions, resulting in early plagioclase saturation, late oxide precipitation, and Fe-enrichment in mid-ocean ridge basalts (MORBs). In contrast, magmas formed above subduction zones are Fe-depleted, have elevated water contents and are more oxidized relative to MORBs. It is widely thought that subduction of hydrothermally altered, oxidized oceanic crust at convergent margins oxidizes the mantle source of arc magmas, resulting in erupted lavas that inherit this oxidized signature. Yet, because our understanding of the calc-alkaline and tholeiitic trends largely comes from studies of erupted melts, the signals from shallow crustal contamination by potentially oxidized, Si-rich, Fe-poor materials, which may also generate calc-alkaline rocks, are obscured. Here, we use deep crustal cumulates to "see through" the effects of shallow crustal processes. We find that the tholeiitic and calc-alkaline trends are indeed reflected in Fe-poor mid-ocean ridge cumulates and Fe-rich arc cumulates, respectively. A key finding is that with increasing crustal thickness, arc cumulates become more Fe-enriched. We propose that the thickness of the overlying crustal column modulates the melting degree of the mantle wedge (lower F beneath thick arcs and vice versa) and thus water and Fe3+ contents in primary melts, which subsequently controls the onset and extent of oxide fractionation. Deep crustal cumulates beneath thick, mature continental arcs are the most Fe-enriched, and therefore may be the "missing" Fe-rich reservoir required to balance the Fe-depleted upper continental crust.

Stable isotope compositions of serpentinite seamounts in the Mariana forearc: Serpentinization processes, fluid sources and sulfur metasomatism

USGS Publications Warehouse

Alt, J.C.; Shanks, Wayne C.

2006-01-01

The Mariana and Izu-Bonin arcs in the western Pacific are characterized by serpentinite seamounts in the forearc that provide unique windows into the mantle wedge. We present stable isotope (O, H, S, and C) data for serpentinites from Conical seamount in the Mariana forearc and S isotope data for Torishima seamount in the Izu-Bonin forearc in order to understand the compositions of fluids and temperatures of serpentinization in the mantle wedge, and to investigate the transport of sulfur from the slab to the mantle wedge. Six serpentine mineral separates have a restricted range of ??18O (6.5-8.5???). Antigorite separates have ??D values of -29.5??? to -45.5??? that reflect serpentinization within the mantle wedge whereas chrysotile has low ??D values (-51.8??? to -84.0???) as the result of re-equilibration with fluids at low temperatures. Fractionation of oxygen isotopes between serpentine and magnetite indicate serpentinization temperatures of 300-375 ??C. Two late cross-fiber chrysotile veins have higher ??18O values of 8.9??? to 10.8??? and formed at lower temperatures (as low as ???100 ??C). Aqueous fluids in equilibrium with serpentine at 300-375 ??C had ??18O = 6.5-9??? and ??D = -4??? to -26???, consistent with sediment dehydration reactions at temperatures <200 ??C in the subducting slab rather than a basaltic slab source. Three aragonite veins in metabasalt and siltstone clasts within the serpentinite flows have ??18O = 16.7-24.5???, consistent with the serpentinizing fluids at temperatures <250 ??C. ??13C values of 0.1-2.5??? suggest a source in subducting carbonate sediments. The ??34S values of sulfide in serpentinites on Conical Seamount (-6.7??? to 9.8???) result from metasomatism through variable reduction of aqueous sulfate (??34S = 14???) derived from slab sediments. Despite sulfur metasomatism, serpentinites have low sulfur contents (generally < 164 ppm) that reflect the highly depleted nature of the mantle wedge. The serpentinites are mostly enriched in 34S (median ??34Ssulfide = 4.5???), consistent with a 34S-enriched mantle wedge as inferred from arc lavas. ?? 2006 Elsevier B.V. All rights reserved.

Inclusions of crichtonite-group minerals in Cr-pyropes from the Internatsionalnaya kimberlite pipe, Siberian Craton: Crystal chemistry, parageneses and relationships to mantle metasomatism

NASA Astrophysics Data System (ADS)

Rezvukhin, Dmitriy I.; Malkovets, Vladimir G.; Sharygin, Igor S.; Tretiakova, Irina G.; Griffin, William L.; O'Reilly, Suzanne Y.

2018-05-01

Cr-pyrope xenocrysts and associated inclusions of crichtonite-group minerals from the Internatsionalnaya kimberlite pipe were studied to provide new insights into processes in the lithospheric mantle beneath the Mirny kimberlite field, Siberian craton. Pyropes are predominantly of lherzolitic paragenesis (Cr2O3 2-6 wt%) and have trace-element spectra typical for garnets from fertile mantle (gradual increase in chondrite-normalized values from LREE to MREE-HREE). Crichtonite-group minerals commonly occur as monomineralic elongated inclusions, mostly in association with rutile, Mg-ilmenite and Cr-spinel within individual grains of pyrope. Sample INT-266 hosts intergrowth of crichtonite-group mineral and Cl-apatite, while sample INT-324 contains polymineralic apatite- and dolomite-bearing assemblages. Crichtonite-group minerals are Al-rich (1.1-4.5 wt% Al2O3), moderately Zr-enriched (1.3-4.3 wt% ZrO2), and are Ca-, Sr-, and occasionally Ba-dominant in terms of A-site occupancy; they also contain significant amounts of Na and LREE. T-estimates and chemical composition of Cr-pyropes imply that samples represent relatively low-T peridotite assemblages with ambient T ranging from 720 to 820°С. Projected onto the 35 mW/m2 cratonic paleogeotherm for the Mirny kimberlite field (Griffin et al., 1999b. Tectonophysics 310, 1-35), temperature estimates yield a P range of 34-42 kbar ( 110-130 km), which corresponds to a mantle domain in the uppermost part of the diamond stability field. The presence of crichtonite-group minerals in Cr-pyropes has petrological and geochemical implications as evidence for metasomatic enrichment of some incompatible elements in the lithospheric mantle beneath the Mirny kimberlite field. The genesis of Cr-pyropes with inclusions of crichtonite-group minerals is attributed to the percolation of Ca-Sr-Na-LREE-Zr-bearing carbonate-silicate metasomatic agents through Mg- and Cr-rich depleted peridotite protoliths. The findings of several potentially new members of the crichtonite group as inclusions in garnet extend existing knowledge on the compositions and occurrences of exotic titanates stable in the lithospheric mantle.

Early mantle heterogeneities in the Réunion hotspot source inferred from highly siderophile elements in cumulate xenoliths

NASA Astrophysics Data System (ADS)

Peters, Bradley J.; Day, James M. D.; Taylor, Lawrence A.

2016-08-01

Ultramafic cumulate rocks form during intrusive crystallization of high-MgO magmas, incorporating relatively high abundances of compatible elements, including Cr and Ni, and high abundances of the highly siderophile elements (HSE: Os, Ir, Ru, Pt, Pd, Re). Here, we utilize a suite of cumulate xenoliths from Piton de la Fournaise, La Réunion (Indian Ocean), to examine the mantle source composition of the Réunion hotspot using HSE abundances and Os isotopes. Dunite and wherlite xenoliths and associated lavas from the Piton de la Fournaise volcanic complex span a range of MgO contents (46 to 7 wt.%), yet exhibit remarkably homogeneous 187Os/188Os (0.1324 ± 0.0014, 2σ), representing the Os-isotopic composition of Réunion hotspot primary melts. A significant fraction of the xenoliths also have primitive upper-mantle (PUM) normalized HSE patterns with elevated Ru and Pd (PUM-normalized Ru/Ir and Pd/Ir of 0.8-6.3 and 0.2-7.2, respectively). These patterns are not artifacts of alteration, fractional crystallization, or partial melting processes, but rather require a primary magma with similar relative enrichments. Some highly olivine-phyric (>40 modal percent olivine) Piton de la Fournaise lavas also preserve these relative Ru and Pd enrichments, while others preserve a pattern that is likely related to sulfur saturation in evolved melts. The estimate of HSE abundances in PUM indicates high Ru/Ir and Pd/Pt values relative to carbonaceous, ordinary and enstatite chondrite meteorite groups. Thus, the existence of cumulate rocks with even more fractionated HSE patterns relative to PUM suggests that the Réunion hotspot samples a yet unrecognized mantle source. The origin of fractionated HSE patterns in Réunion melts may arise from sampling of a mantle source that experienced limited late accretion (<0.2% by mass) compared with PUM (0.5-0.8%), possibly involving impactors that were distinct from present-day chondrites, or limited core-mantle interactions. Given the remarkably homogeneous Os, Pb, and noble-gas isotopic signatures of Réunion, which plot near the convergence point of isotopic data for many hotspots, such a conclusion provides evidence for an early differentiated and subsequently isolated mantle domain that may be partially sampled by some ocean island basalts.

Origin of the DUPAL anomaly in mantle xenoliths of Patagonia (Argentina) and geodynamic consequences

NASA Astrophysics Data System (ADS)

Mazzucchelli, Maurizio; Cipriani, Anna; Hémond, Christophe; Zanetti, Alberto; Bertotto, Gustavo Walter; Cingolani, Carlos Alberto

2016-04-01

The sub-continental lithospheric mantle of South America has been known for some time to carry the DUPAL isotope anomaly as seen in volcanics from the Paraná volcanic province. However, this has not allowed discriminating whether the DUPAL anomaly is a primary feature of the mantle source or acquired during the upwelling and emplacement of the primary magmas. We discovered mantle xenoliths from the Tres Lagos location in Patagonia that carry evidence of percolation by metasomatic melts that imparted the DUPAL isotope anomaly signature. We discuss a model that requires four isotope components (LCC, EM2, HIMU and DM) to account for the Sr, Nd and Pb isotope variability of our samples. We propose that upwelling of hot astenosphere during the Miocene could have triggered the melting of the LCC and EM2 components carrying the DUPAL anomaly, previously entrained in the subcontinental mantle by subduction. These ascending melts would have then metasomatised the local SCLM characterised by DMM and HIMU geochemical affinity generating the hybrid DUPAL-bearing mantle sampled by the Tres Lagos xenoliths.

Methanol ice in the protostar GL 2136

NASA Technical Reports Server (NTRS)

Skinner, C. J.; Tielens, A. G. G. M.; Barlow, M. J.; Justtanont, K.

1992-01-01

We present ground-based spectra in the 10 and 20 micron atmospheric windows of the deeply embedded protostar GL 2136. These reveal narrow absorption features at 9.7 and 8.9 microns, which we ascribe to the CO-stretch and CH3 rock (respectively) of solid methanol in grain mantles. The peak position of the 9.7 micron band implies that methanol is an important ice mantle component. However, the CH3OH/H2O abundance ratio derived from the observed column densities is only 0.1. This discrepancy suggests that the solid methanol and water ice are located in independent grain components. These independent components may reflect chemical differentiation during grain mantle formation and/or partial outgassing close to the protostar.

Deep mantle cycling of oceanic crust: evidence from diamonds and their mineral inclusions.

PubMed

Walter, M J; Kohn, S C; Araujo, D; Bulanova, G P; Smith, C B; Gaillou, E; Wang, J; Steele, A; Shirey, S B

2011-10-07

A primary consequence of plate tectonics is that basaltic oceanic crust subducts with lithospheric slabs into the mantle. Seismological studies extend this process to the lower mantle, and geochemical observations indicate return of oceanic crust to the upper mantle in plumes. There has been no direct petrologic evidence, however, of the return of subducted oceanic crustal components from the lower mantle. We analyzed superdeep diamonds from Juina-5 kimberlite, Brazil, which host inclusions with compositions comprising the entire phase assemblage expected to crystallize from basalt under lower-mantle conditions. The inclusion mineralogies require exhumation from the lower to upper mantle. Because the diamond hosts have carbon isotope signatures consistent with surface-derived carbon, we conclude that the deep carbon cycle extends into the lower mantle.

Cretaceous potassic intrusives with affinities to aillikites from Jharia area: Magmatic expression of metasomatically veined and thinned lithospheric mantle beneath Singhbhum Craton, Eastern India

NASA Astrophysics Data System (ADS)

Srivastava, Rajesh K.; Chalapathi Rao, N. V.; Sinha, Anup K.

2009-11-01

Cretaceous potassic dykes and sills at the Jharia area intrude the Permo-carboniferous coal-bearing Gondwana sediments of the Eastern Damodar Valley, Singhbhum craton. These intrusives are widely regarded as a part of the Mesozoic alkaline and Rajmahal flood basalt magmatism in the Eastern Indian shield. Jharia intrusives display a wide petrographic diversity; olivine, phlogopite and carbonate are the predominant phases whereas apatite and rutile constitute important accessories. Impoverishment in sodium, silica and alumina and enrichment in potassium, titanium and phosphorous are the hallmark of these rocks and in this aspect they are strikingly similar to the rift-related aillikites (ultramafic lamprophyres) of Aillik Bay, Labrador. Crustal contamination of the Jharia magmas is minimal and the incompatible trace element ratios demonstrate (i) their generation by greater degrees of partial melting of a sub-continental lithospheric mantle (SCLM) source similar to that of the kimberlites of Dharwar craton, southern India, and (ii) retention of long-term memories of ancient (Archaean) subduction experienced by their source regions. We infer that a metasomatically veined and thinned lithosphere located at the margin of the Singhbhum craton and the inheritance of an ancient (Archaean) subducted component has played a significant role in deciding the diverging petrological and geochemical characters displayed by the Jharia potassic intrusives: those of kimberlites (orangeites) and lamproites (cratonic signature) and those of aillikites (rift-related signature). A substantial melt component of Jharia potassic intrusives was derived from the SCLM and the melt contribution of the Kerguelen plume is inferred to be minimal.

Constraints on the differentiation of the Earth from the coupled Sm-146,147-Nd-142,143 systematics

NASA Technical Reports Server (NTRS)

Jacobsen, S. B.; Harper, C. L., Jr.

1993-01-01

The coupled Sm-Nd systematics are a powerful (albeit analytically challenging) tool for investigating the geodynamic history of the Earth. We have previously reported evidence for a 33 ppm difference of an Isua sample relative to our terrestrial standard. Interpretation yields a formation age range for the depleted mantle (DM) source reservoir of 4.45-4.55 Ga. This is consistent with an epoch of LREE-enriched melt extraction from the mantle (proto-crust formation), soon after magma ocean freeze-up following the putative Moon forming giant impact.

Mass-dependent Mo isotope variations in oceanic basalts - a new tracer for mantle recycling processes

NASA Astrophysics Data System (ADS)

Willbold, M.; Freymuth, H.; Hibbert, K.; Lai, Y. J.; Elliott, T.

2016-12-01

How and to what extent crustal material is recycled into the deeper mantle as a result of plate tectonic processes is a long-standing but still not fully understood question in Earth Sciences. Indirect evidence from chemical as well as radiogenic isotope data in oceanic basalts suggest that such a process may indeed have operated over much of Earth's history. Yet, uncertainties in characterising the age of the presumed recycled crustal components as well as the wide range in their chemical composition do not allow us to verify the mantle recycling hypothesis. Technological advances now enable us to explore new isotopic tracers that could shed light on this question. One of these new tools are mass-dependent isotope variation of molybdenum (Mo). Mass-dependent Mo isotope data in clastic and chemical sediments are a well-established geochemical tool to study redox conditions in the Earth's water masses over the geological past [1, 2, 3]. Being an intrinsic property of rocks exposed to the hydrosphere (see Anbar [4] for an overview), mass-dependent Mo isotope variation in mantle-derived rocks from oceanic settings could therefore be used a tracer of recycled crustal material in the Earth's mantle. In this contribution we provide a current overview over how different geological and magmatic processes - such as seawater alteration of oceanic crust, slab dehydration during plate subduction as well as magmatic emplacement - could affect the Mo isotopic composition of crustal components being transferred into the deeper mantle, as well as that of mantle melts that may contain such a recycled component. With this in mind, we explore the use of mass-dependent Mo isotope variations in mantle-derived rocks as a tracer of recycled crust in the mantle. [1] Archer & Vance (2008) Nature Geoscience 1, 597-600. [2] Barling et al. (2001) EPSL 193, 447-457. [3] Siebert et al. (2003) EPSL 211, 159-171. [4] Anbar (2004) Rev. Min. Geochem. 55, 429-454.

Isotopic composition of reduced and oxidized sulfur in the Canary Islands: implications for the mantle S cycle

NASA Astrophysics Data System (ADS)

Beaudry, P.; Longpre, M. A.; Wing, B. A.; Bui, T. H.; Stix, J.

2017-12-01

The Earth's mantle contains distinct sulfur reservoirs, which can be probed by sulfur isotope analyses of volcanic rocks and gases. We analyzed the isotopic composition of reduced and oxidized sulfur in a diverse range of volcanically derived materials spanning historical volcanism in the Canary Islands. Our sample set consists of subaerial volcanic tephras from three different islands, mantle and sedimentary xenoliths, as well as lava balloon samples from the 2011-2012 submarine El Hierro eruption and associated crystal separates. This large sample set allows us to differentiate between the various processes responsible for sulfur isotope heterogeneity in the Canary archipelago. Our results define an array in triple S isotope space between the compositions of the MORB and seawater sulfate reservoirs. Specifically, the sulfide values are remarkably homogeneous around d34S = -1 ‰ and D33S = -0.01 ‰, while sulfate values peak at d34S = +4 ‰ and D33S = +0.01 ‰. Lava balloons from the El Hierro eruption have highly enriched sulfate d34S values up to +19.3 ‰, reflecting direct interaction between seawater sulfate and the erupting magma. Several sulfate data points from the island of Lanzarote also trend towards more positive d34S up to +13.8 ‰, suggesting interaction with seawater sulfate-enriched lithologies or infiltration of seawater within the magmatic system. On the other hand, the modal values and relative abundances of S2- and S6+ in crystal separates suggest that the Canary Island mantle source has a d34S around +3 ‰, similar to the S-isotopic composition of a peridotite xenolith from Lanzarote. We infer that the S2- and S6+ modes reflect isotopic equilibrium between those species in the magmatic source, which requires 80 % of the sulfide to become oxidized after melting, consistent with measured S speciation. This 34S enrichment of the source could be due to the recycling of hydrothermally-altered oceanic crust, which has been previously suggested for the Canary Island hotspot on the basis of radiogenic isotope characteristics.

The origin of alkaline magmas in an intraplate setting near a subduction zone: the Ngatutura Basalts, North Island, New Zealand

NASA Astrophysics Data System (ADS)

Briggs, R. M.; Utting, A. J.; Gibson, I. L.

1990-01-01

The Ngatutura Basalts are one of a series of Pliocene-Quaternary alkalic basalt volcanic fields in North Island, New Zealand. They are situated in an intraplate tectonic setting behind the currently active Taupo Volcanic Zone, and 300 km above the subducting slab. The volcanic field consists of 16 small-volume monogenetic volcanic centres composed mainly of eroded scoria cones and lava flows, that occupy an extensional tectonic environment characterized by NE-striking block faulting. In some cases the faults have controlled the localization of volcanic vents. The lavas have restricted compositions, ranging from hawaiites to nepheline hawaiites, and are characterized by enriched LILE, LREE, and HFS elements, with particularly high Nb and Ta, low Ba/Nb, and high Zr/Y and Ce N/Yb N ratios. Nepheline hawaiites are slightly more differentiated than hawaiites and have higher Ce N/Yb N ratios. Petrogenetic modelling suggests that the range in composition was mainly controlled by fractional crystallization of olivine, clinopyroxene, and minor plagioclase and titanomagnetite, which is consistent with the modal phenocryst abundances. Fractionation is explained by side-wall crystallization and flowage differentiation during rapid ascent, rather than gravitative settling in a magma chamber. Ngatutura magmas were probably derived from an enriched garnet lherzolite source within the low-velocity mantle. The process of source enrichment is speculative but our preferred model calls on metasomatizing fluids in the low-velocity zone. There is no geochemical evidence for any influence of the subducted slab on their composition, even though they overlie the Pacific plate subduction zone. This implies that the extent of subduction-related contamination in the mantle wedge is not pervasive, but is confined to a limited region overlying the subducted slab. Also, the "deep mantle plume" responsible for alkalic magmatism must have originated above the slab, because it seems unlikely that such a plume could have occurred at a deeper level and penetrate the slab without some evidence. This therefore limits the depth of origin of these "deep mantle plumes" to less than 300 km.

Evidence for an eolian origin for the silt-enriched soil mantles on the glaciated uplands of eastern Upper Michigan, USA

USGS Publications Warehouse

Schaetzl, R.J.; Loope, W.L.

2008-01-01

We provide textural, geochemical, and mineralogical data on a thin, silty deposit that unconformably mantles glaciated uplands in the eastern Upper Peninsula of Michigan. Previous research on this deposit, which we hypothesize to be loess, is nonexistent. The uplands were islands or narrow peninsulas within one or more glacial lakes. We compare the distribution, likely source and nature of the 20-60??cm thick silty mantle by using the loess formation model of Mason et al. [Mason, J.A., Nater, E.A., Zanner, C.W., Bell, J.C., 1999. A new model of topographic effects on the distribution of loess. Geomorphology 28, 223-236], which focuses on the generation of eolian silt by saltating sand across upwind, barren surfaces. Parabolic dunes, with arms open to the NW, are common on former lake floors upwind of the silt-mantled uplands, attesting to the strength and direction of paleowinds. The abrupt termination of the dunes at the footslopes of the uplands, associated with silt deposition on upland soil surfaces in downwind locations, are both consistent with the model of Mason et al. [Mason, J.A., Nater, E.A., Zanner, C.W., Bell, J.C., 1999. A new model of topographic effects on the distribution of loess. Geomorphology 28, 223-236]. Sediments on former lake floors contain abundant strata of fine/medium sand and silt, and thus are likely sources for the silt and dune sand. The cap, dune and lake sediments are similar along many different geochemical axes, whereas the substrate sediment, i.e., the drift below the cap, is unique. Cap sediments, normally containing roughly 30% silt, are enriched in quartz and depleted in Ti and Zr, relative to dune sediment. The dune sediment, a more residual eolian deposit, is enriched in Ti and Zr, relative to the cap, probably due to its greater abundance of heavy minerals. Therefore, we conclude that the silty cap is loess that was deflated from abandoned lake floors after nearby glacial lakes drained, probably contemporaneously with dune migration across the former lake floors. ?? 2008 Elsevier B.V. All rights reserved.

Platinum-group element abundance and distribution in chromite deposits of the Acoje Block, Zambales Ophiolite Complex, Philippines

USGS Publications Warehouse

Bacuta, G.C.; Kay, R.W.; Gibbs, A.K.; Lipin, B.R.

1990-01-01

Platinum-group elements (PGE) occur in ore-grade concentration in some of the chromite deposits related to the ultramafic section of the Acoje Block of the Zambales Ophiolite Complex. The deposits are of three types: Type 1 - associated with cumulate peridotites at the base of the crust; Type 2 - in dunite pods from the top 1 km of mantle harzburgite; and Type 3 - like Type 2, but in deeper levels of the harzburgite. Most of the deposites have chromite compositions that are high in Cr with Cr/(Cr + Al) (expressed as chromium index, Cr#) > 0.6; high-Al (Cr# Pd, thought to be characteristic of PGE-barren deposits) and positive slope (Ir < Pd, characteristic of PGE-rich deposits). Iridium, Ru and Os commonly occur as micron-size laurite (sulfide) inclusions in unfractured chromite. Laurite and native Os are also found as inclusions in interstitial sulfides. Platinum and Pd occur as alloy inclusions (and possibly as solid solution) in interstitial Ni-Cu sulfides and as tellurobismuthides in serpentine and altered sulfides. Variability of PGE distribution may be explained by alteration, crystal fractionation or partial melting processes. Alteration and metamorphism were ruled out, because PGE contents do not correlate with degree of serpentinization or the abundance and type (hydroxyl versus non-hydroxyl) of silicate inclusions in chromite. Preliminary Os isotopic data do not support crustal contamination as a source of the PGEs in the Acoje deposits. The anomalous PGE concentrations in Type 1 high-Cr chromite deposits are attributed to two stages of enrichment: an early enrichment of their mantle source from previous melting events and a later stage of sulfide segregation accompanying chromite crystallization. High-Al chromite deposits which crystallized from basalts derived from relatively low degrees of melting owe their low PGE content to partitioning of PGEs in sulfides and alloys that remain in the mantle. High-Cr deposits crystallized from melts that were previously enriched with PGEs during early melting events of their mantle source; Pt and Pd ore concentrations (ppm levels) are attained by segregation of magmatic sulfides. The Acoje deposits indicate that ophiolites are a potential economic source of the PGEs. ?? 1990.

Geochemistry of the Neoproterozoic metabasic rocks from the Negele area, southern Ethiopia: Tectonomagmatic implications

NASA Astrophysics Data System (ADS)

Yihunie, Tadesse; Adachi, Mamoru; Yamamoto, Koshi

2006-03-01

Neoproterozoic metabasic rocks along with metasediments and ultramafic rocks constitute the Kenticha and Bulbul lithotectonic domains in the Negele area. They occur as amphibolite and amphibole schist in the Kenticha, and amphibole schist and metabasalt in the Bulbul domains. These rocks are dominantly basaltic in composition and exhibit low-K tholeiitic characteristics. They are slightly enriched in large ion lithophile (LIL) and light rare earth (LRE) elements and depleted in high field strength (HFS) and heavy rare earth (HRE) elements. They exhibit chemical characteristics similar to back-arc basin and island-arc basalts, but include a few samples with slightly higher Y, Zr and Nb contents. Initial Sr isotopic ratios and ɛNd values for the Kenticha metabasic rocks range from 0.7048 to 0.7051 and from 4.7 to 9.6 whereas for the Bulbul metabasic rocks they range from 0.7032 to 0.7055 and from -0.1 to 5.5, respectively. The trace elements and Sr-Nd isotope compositions of samples from the Kenticha and Bulbul domains suggest similar, but isotopically heterogeneous magma sources. The magma is inferred to have derived from depleted source with a contribution from an enriched mantle source component.

A snapshot of mantle metasomatism: Trace element analysis of coexisting fluid (LA-ICP-MS) and silicate (SIMS) inclusions in fibrous diamonds

NASA Astrophysics Data System (ADS)

Tomlinson, E. L.; Müller, W.; EIMF

2009-03-01

We have determined the trace element compositions of coexisting fluid (carbonate-K-chloride-H 2O) and single-phase mineral inclusions in peridotitic (Cr-diopside) and eclogitic (omphacite, garnet) inclusions in fibrous diamonds from the Panda kimberlite (Slave craton, Canada). These diamonds provide a unique insight into the nature of the metasomatic agent, the metasomatised minerals and the pre-metasomatic protolith. The fluid component is strongly enriched in light rare earth elements (LREE) and large ion lithophile elements (LILE). Co-existing peridotitic minerals record a melt extraction event (high Cr and Ni) in the protolith prior to the influx of the trapped metasomatic fluid. The silicate minerals are also strongly enriched in LREE. Calculated partition coefficients agree with experimentally determined values in the literature, despite the complex composition of the natural fluid. This indicates that the minerals have re-equilibrated with the metasomatic fluid. The trace element compositions of the mineral inclusions are comparable to many equivalent phases in monocrystalline diamonds. This suggests that the metasomatic fluid and the process recorded in these samples may also be responsible for the growth of some types of monocrystalline diamonds.

The Ellsworth terrane, coastal Maine: Geochronology, geochemistry, and Nd-Pb isotopic composition - Implications for the rifting of Ganderia

USGS Publications Warehouse

Schulz, K.J.; Stewart, D.B.; Tucker, R.D.; Pollock, J.C.; Ayuso, R.A.

2008-01-01

The Ellsworth terrane is one of a number of fault-bounded blocks that occur along the eastern margin of Ganderia, the western-most of the peri-Gondwanan domains in the northern Appalachians that were accreted to Laurentia in the Paleozoic. Geologic relations, detrital zircon ages, and basalt geochemistry suggest that the Ellsworth terrane is part of Ganderia and not an exotic terrane. In the Penobscot Bay area of coastal Maine, the Ellsworth terrane is dominantly composed of bimodal basalt-rhyolite volcanic sequences of the Ellsworth Schist and unconformably overlying Castine Volcanics. We use new U-Pb zircon geochronology, geochemistry, and Nd and Pb isotopes for these volcanic sequences to constrain the petrogenetic history and paleotectonic setting of the Ellsworth terrane and its relationship with Ganderia. U-Pb zircon geochronology for rhyolites indicates that both the Ellsworth Schist (508.6 ?? 0.8 Ma) and overlying Castine Volcanics (503.5 ?? 2.5 Ma) are Middle Cambrian in age. Two tholefitic basalt types are recognized. Type Tb-1 basalt, present as pillowed and massive lava flows and as sills in both units, has depleted La and Ce ([La/Nd]N = 0.53-0.87) values, flat heavy rare earth element (REE) values, and no positive Th or negative Ta anomalies on primitive mantle-normalized diagrams. In contrast, type Th-2 basalt, present only in the Castine Volcanics, has stightly enriched LREE ([La/Yb]N = 1.42-2.92) values and no Th or Th anomalies. Both basalt types have strongly positive ??Nd (500) values (Th-1 = +7.9-+8.6; Th-2 = +5.6-+7.0) and relatively enriched Pb isotopic compositions (206Ph/204Pb = 18.037-19.784; 207/204Pb = 15.531-15.660; 2088Pb/204Pb = 37.810-38.817). The basalts have compositions transitional between recent normal and enriched mid-ocean-ridge basalt, and they were probably derived by partial melting of compositionatly heterogeneous asthenosphenc mantle. Two types of rhyolite also are present. Type R-1 rhyolite, which mostly occurs as tuffs interlayered with basalt in the Ellsworth Schist, is calc-alkaline and characterized by relatively low REE, Zr, and Hf contents, enriched LREE ([La/Yb]N ???3-6), positive Th and negative Th anomalies, ??Nd (500) values near zero (+0.5 to -0.9), and relatively unradiogenic Ph isotope values (206Pb/204Pb = 18.845; 207Pb/ 204Pb = 15.625; 208Pb/204Pb = 38.626). The data suggest that R-1 rhyolite magma was Likely derived by mixing of basalt with melts from a relatively depleted crustal source. Type R-2 rhyolite, which mostly occurs as lava flows and domes in the Castine volcanics, is tholeiitic and characterized by enriched REE with flat patterns ([La/Yb]N = 1-2.5), moderate negative Eu anomalies (Eu/Eu* = 0-34.5), enriched Th, small negative Th anomalies, and ??Nd (500) (+5.8-+7.5) and Ph isotope (206Pb/204Pb = 19.175-19.619; 207Pb/204Pb = 15.605--15.649; 208Pb/204Pb = 38.834-38.851) values that overlap those of the tholeiitic basalts. The data suggest that R-2 rhyolite magma was derived by the partial melting of hydrothermally altered basalt with the addition of a small amount of an enriched component, probably R-1 rhyolite. The geololic, geochemicai, and isotopic characteristics of the bimodal volcanic sequences strongly suggest that the Ellsworth terrane did not evolve as an extensional back-arc basin behind an active arc, but rather it evolved as a proto-oceanic rift petrogenetically similar to Cenozoic rifts like the Gulf of California-Salton mrough and Red Sea-Gulf of Aden rift systems. Such a setting is supported by the presence of serpentinized mantle and zinc-copper-rich massive sulfide deposits in the Ellsworth terrane. We conclude that the Ellsworth terrane developed as a Mid

Basin Excavation, Lower Crust, Composition, and Bulk Moon Mass balance in Light of a Thin Crust

NASA Technical Reports Server (NTRS)

Jolliff, B. L.; Korotev, R. L.; Ziegler, R. A.

2013-01-01

New lunar gravity results from GRAIL have been interpreted to reflect an overall thin and low-density lunar crust. Accordingly, crustal thickness has been modeled as ranging from 0 to 60 km, with thinnest crust at the locations of Crisium and Moscoviense basins and thickest crust in the central farside highlands. The thin crust has cosmochemical significance, namely in terms of implications for the Moon s bulk composition, especially refractory lithophile elements that are strongly concentrated in the crust. Wieczorek et al. concluded that the bulk Moon need not be enriched compared to Earth in refractory lithophile elements such as Al. Less Al in the crust means less Al has been extracted from the mantle, permitting relatively low bulk lunar mantle Al contents and low pre- and post-crust-extraction values for the mantle (or the upper mantle if only the upper mantle underwent LMO melting). Simple mass-balance calculations using the method of [4] suggests that the same conclusion might hold for Th and the entire suite of refractory lithophile elements that are incompatible in olivine and pyroxene, including the KREEP elements, that are likewise concentrated in the crust.

High Ni in Archean tholeiites

NASA Astrophysics Data System (ADS)

Arndt, Nicholas T.

1991-03-01

Archean tholeiites generally have higher Ni, Co. Cr and Fe than most younger tholeiites with similar MgO contents. These characteristics cannot be attributed to high T or P batch melting in the Archean mantle, because, although such melts are enriched in siderophile elements, they have higher MgO than normal tholeiites. As primary melts fractionate to lower MgO, they lose Ni, Co and Cr. Nor can the differences between Archean and younger tholeiites be attributed to secular variation in mantle compositions because Archean komatiites have Ni, Co, Cr contents similar to modern (Gorgona) komatiites. It is suggested that the high siderophile element content of Archean tholeiites results from mixing of either komatiitic with basaltic magmas, as might occur in an ascending, melting mantle plume or column, or of komatiite and more evolved rocks, as may take place when komatiite encounters and assimilates crustal rocks.

Synthesis of NH4-Substituted Muscovite at 6.3 GPa and 1000°C: Implications for Nitrogen Transport to the Earth's Mantle

NASA Astrophysics Data System (ADS)

Sokol, A. G.; Sokol, E. V.; Kupriyanov, I. N.; Sobolev, N. V.

2018-03-01

The synthesis of NH4-bearing muscovite at P = 6.3 GPa and T = 1000°C in equilibrium with NH3-H2O fluid is performed. It is determined that the newly formed muscovite is enriched in celadonite minal and contains 370 ppm of NH4. The obtained data make it possible to conclude that ammonium-bearing micas have sufficient thermal stability and can transport crustal nitrogen to the mantle in the presence of a reduced water-ammonia fluid at fO2 less than the values of IW + 2 log units even in the regime of "hot" subduction. The key parameter that determines the efficiency of this mechanism for the deep nitrogen cycle is redox stability of NH4-bearing muscovite at the mantle PT-parameters.

Magma Mixing: Why Picrites are Not So Hot

NASA Astrophysics Data System (ADS)

Natland, J. H.

2010-12-01

Oxide gabbros or ferrogabbros are the late, low-temperature differentiates of tholeiitic magma and usually form as cumulates that can have 2-30% of the magmatic oxides, ilmenite and magnetite. They are common in the ocean crust and are likely ubiquitous wherever extensive tholeiitic magmatism has occurred, especially beneath thick lava piles such as at Hawaii, Iceland, oceanic plateaus, island arcs and ancient continental crust. When intruded by hot primitive magma including picrite, the oxide-bearing portions of these rocks are readily partially melted or assimilated into the magma and contribute to it a degree of iron and titanium enrichment that is not reflective of the mantle source of the primitive magma. The most extreme examples of such mixing are meimechites and ferropicrites, but this type of end-member mixing is even common in MORB. To the extent this process occurs, the eruptive picrite cannot be used to estimate compositions of partial melts of mantle rocks, nor their eruptive or potential temperatures, using olivine-liquid FeO-MgO backtrack procedures. Most picrites have glasses with compositions approximating those expected from low-pressure multiphase cotectic crystallization, and olivine that on average crystallized from liquids of nearly those compositions. The hallmark of such rocks is the presence of minerals other than olivine among phenocrysts (plagioclase at Iceland, clinopyroxene at many oceanic islands), Fe- and Ti-rich chromian spinel (ankaramites, ferropicrites and meimichites), and in some cases the presence of iron-rich olivine (hortonolite ~Fo65 in ferropicrites), Ti-rich kaersutitic amphibole and even apatite (meimechites); the latter two derive from late-stage, hydrous and geochemically enriched metamorphic or alkalic assimilants. This type of mixing, however, does not necessarily involve depleted and enriched mixing components. To avoid such mixing, primitive melts have to rise primarily through upper mantle rocks of near-zero melt porosity in regions where crustal-level magma chambers and flanking rift zones do not have a chance to form. Low-magma supply is favored. In the ocean basins, such upper mantle mainlining occurs only at certain fracture zones, deep propagating rifts at microplates, or ultra-slow spreading ridges, but no liquids (glasses) with >10% MgO occur at any of these places. On continents, rift structures through cratons might allow this, but so far no picrite, ferropicrite, or meimichite that has been adequately described from these places lacks evidence for end-member mixing. Low-temperature iron-rich magmas can accumulate in the deep lower crust and later rise to form substantial intrusions (e.g. Skaergaard) or erupt as flood basalts (Columbia River). Some komatiites might represent high-temperature liquids, but many are so altered that original liquid compositions cannot be deduced (e.g., Gorgona). The hottest intraplate volcano is Kilauea, Hawaii, where rare picrite glass with 15% MgO has an estimated eruptive temperature (1) of ~1350C and a potential temperature at 1 GPa of ~1420C. Lavas at all other linear island chains, Iceland and even west Greenland where picrites are abundant, are cooler than this. (1) Beattie, P., 1993. CMP 115: 103-111.

Formation and modification of chromitites in the mantle

NASA Astrophysics Data System (ADS)

Arai, Shoji; Miura, Makoto

2016-11-01

Podiform chromitites have long supplied us with unrivaled information on various mantle processes, including the peridotite-magma reaction, deep-seated magmatic evolution, and mantle dynamics. The recent discovery of ultrahigh-pressure (UHP) chromitites not only sheds light on a different aspect of podiform chromitites, but also changes our understanding of the whole picture of podiform chromitite genesis. In addition, new evidence was recently presented for hydrothermal modification/formation chromite/chromitite in the mantle, which is a classical but innovative issue. In this context, we present here an urgently needed comprehensive review of podiform chromitites in the upper mantle. Wall-rock control on podiform chromitite genesis demonstrates that the peridotite-magma reaction at the upper mantle condition is an indispensable process. We may need a large system in the mantle, far larger than the size of outcrops or mining areas, to fulfill the Cr budget requirement for podiform chromitite genesis. The peridotite-magma reaction over a large area may form a melt enriched with Na and other incompatible elements, which mixes with a less evolved magma supplied from the depth to create chromite-oversaturated magma. The incompatible-element-rich magma trapped by the chromite mainly precipitates pargasite and aspidolite (Na analogue of phlogopite), which are stable under upper mantle conditions. Moderately depleted harzburgites, which contain chromite with a moderate Cr# (0.4-0.6) and a small amount of clinopyroxene, are the best reactants for the chromitite-forming reaction, and are the best hosts for podiform chromitites. Arc-type chromitites are dominant in ophiolites, but some are of the mid-ocean ridge type; chromitites may be common beneath the ocean floor, although it has not yet been explored for chromitite. The low-pressure (upper mantle) igneous chromitites were conveyed through mantle convection or subduction down to the mantle transition zone to form ultrahigh-pressure chromitites. Some of these reappear at the shallower mantle, and can coexist with newly formed low-pressure igneous chromitites. High-temperature hydrothermal fluids can dissolve and precipitate chromite, and hydrothermal chromitites (chromitites precipitated from aqueous fluids) are possibly formed within the mantle where the circulation of hydrous fluid is available, e.g., at the mantle wedge.

The causes for geographical variations in OS187/OS186 at the Cretaceous-Tertiary boundary

NASA Technical Reports Server (NTRS)

Turekian, K. K.; Esser, B. K.; Ravizza, G. E.

1988-01-01

Researchers at Yale has approached the problem of the osmium isotopic composition of marine deposits formed in contact with both oxidized and reduced bottom waters. The measured (187) Os/(186) Os ratios of modern bulk sediment can be explained using mixing equations involving continental detrital, volcaniclastic, cosmogenic and hydrogeneous components. These studies show that sediments deposited under reducing marine conditions contain a hydrogenous component which is enriched in Re and has a radiogenic (187) Os/(186) Os ratio. The presence of such a hydrogenous component in the marine fish clay at Stevns Klint can account for the elevation of its (187) Os/(186) Os ration above the expected meteoritic value. Mass balance considerations require the Re/Os ratio of the phase precipitated from the terminal Cretaceous sea at Stevns Klint to have been about one tenth the value observed in contemporary deposits in the Black Sea, assuming Re has not been lost (or Os gained) subsequent to precipitation. In continental sections, the elevation of the (187) Os/(186) Os ratio in boundary layers may be due to precipitation from continental waters of crustally-derived radiogenic osmium either contemporaneous with the meteoritic (or mantle) osmium deposition or later during diagenesis.

Nd-isotopes in selected mantle-derived rocks and minerals and their implications for mantle evolution

USGS Publications Warehouse

Basu, A.R.; Tatsumoto, M.

1980-01-01

The Sm-Nd systematics in a variety of mantle-derived samples including kimberlites, alnoite, carbonatite, pyroxene and amphibole inclusions in alkali basalts and xenolithic eclogites, granulites and a pyroxene megacryst in kimberlites are reported. The additional data on kimberlites strengthen our earlier conclusion that kimberlites are derived from a relatively undifferentiated chondritic mantle source. This conclusion is based on the observation that the e{open}Nd values of most of the kimberlites are near zero. In contrast with the kimberlites, their garnet lherzolite inclusions show both time-averaged Nd enrichment and depletion with respect to Sm. Separated clinopyroxenes in eclogite xenoliths from the Roberts Victor kimberlite pipe show both positive and negative e{open}Nd values suggesting different genetic history. A whole rock lower crustal scapolite granulite xenolith from the Matsoku kimberlite pipe shows a negative e{open}Nd value of -4.2, possibly representative of the base of the crust in Lesotho. It appears that all inclusions, mafic and ultramafic, in kimberlites are unrelated to their kimberlite host. The above data and additional Sm-Nd data on xenoliths in alkali basalts, alpine peridotite and alnoite-carbonatites are used to construct a model for the upper 200 km of the earth's mantle - both oceanic and continental. The essential feature of this model is the increasing degree of fertility of the mantle with depth. The kimberlite's source at depths below 200 km in the subcontinental mantle is the most primitive in this model, and this primitive layer is also extended to the suboceanic mantle. However, it is clear from the Nd-isotopic data in the xenoliths of the continental kimberlites that above 200 km the continental mantle is distinctly different from their suboceanic counterpart. ?? 1980 Springer-Verlag.

Chlorine isotope evidence for crustal recycling into the Earth's mantle

NASA Astrophysics Data System (ADS)

John, Timm; Layne, Graham D.; Haase, Karsten M.; Barnes, Jaime D.

2010-09-01

Subduction of oceanic lithosphere is a key feature of terrestrial plate tectonics. However, the effect of this recycled crustal material on mantle composition is debated. Ocean island basalts (OIB) provide direct insights into the composition of Earth's mantle. The distinct composition of the HIMU (high 238U/ 204Pb)- and EM (enriched mantle)-type OIB mantle sources may be due to either recycling of oceanic crust and sediment into the mantle or metasomatic processes within the mantle. Chlorine derived from seawater or crustal fluids potentially provides a tracer for recycled material. Previously reported δ 37Cl values for mid-ocean ridge basalts (MORB) range from ca. - 3.0 to near 0‰. In contrast to MORB, we find a larger variation in OIB glasses representing HIMU- and EM-type mantle sources based on replicate SIMS analyses with δ 37Cl values ranging from - 1.6 to + 1.1‰ for HIMU-type and - 0.4 to + 2.9‰ for EM-type lavas. These δ 37Cl values correlate positively with 87Sr/ 86Sr ratios for both the HIMU- and EM-type samples. The negative δ 37Cl values of some HIMU-type lavas overlap with those of altered oceanic lithosphere, which is assumed to be present in the HIMU source. The EM lavas have high 87Sr/ 86Sr and primarily positive δ 37Cl values. We hypothesize that subducting sediments may have developed high δ 37Cl values by expelling 37Cl-depleted pore fluids, thus accounting for the positive δ 37Cl values recorded in the EM-type lavas.

Rhenium - osmium heterogeneity of enriched mantle basalts explained by composition and behaviour of mantle-derived sulfides

NASA Astrophysics Data System (ADS)

Harvey, J.; Dale, C. W.; Gannoun, A.; Burton, K. W.

2010-12-01

Analyses of enriched mantle (EM) -basalts, using lithophile element-based isotope systems have long provided evidence for discrete, but variable mantle reservoirs [1]. Upon partial melting, the isotopic fingerprint of each reservoir is imparted upon the partial melt produced. However, recent work involving the Re-Os isotope systematics of EM-basalts [2] suggests that it may not be so simple to delimit these previously well defined mantle reservoirs; the “mantle zoo” [3] may contain more reservoirs than previously envisaged. However, a simple model, with varying contributions from two populations of compositionally distinct mantle sulfides can readily account for the observed heterogeneities in Re-Os isotope systematics of such basalts without additional mantle reservoirs. Rhenium-osmium elemental and isotopic analyses of individual sulfide grains separated from spinel lherzolites from Kilbourne Hole, NM, USA demonstrate that two discrete populations of mantle sulfide exist in terms of both Re-Os systematics and textural relationship with co-existing silicates. One population, with a rounded morphology, is preserved in silicate grains and typically possesses high [Os], low [Re] with unradiogenic, typically sub-chondritic, 187Os/188Os attributable to long term isolation in a low-Re environment. By contrast, irregular-shaped sulfides, preserved along silicate grain boundaries, possess low [Os], higher [Re] and a wider range of, but generally supra-chondritic, 187Os/188Os ([Os] typically ≤ 1-2 ppm, 187Os/188Os ≤ 0.3729; this study). This population is thought to represent metasomatic sulfide (e.g. [4,5]). Uncontaminated silicate phases contain negligible Os (<100 ppt) therefore the Os elemental and isotope composition of basalts is dominated by volumetrically insignificant sulfide ([Os] ≤ 37 ppm, this study). During the early stages of partial melting, supra-chondritic interstitial sulfides are mobilized and incorporated into the melt, adding their radiogenic 187Os/188Os signature. Only when sulfides armored within silicates are exposed to the melt through continued partial melting will enclosed sulfides add their high [Os] and unradiogenic 187Os/188Os to the aggregate melt. Platinum-group element data for whole rocks are also consistent with this scenario. The sequence of (i) addition of all the metasomatic sulfide, followed by (ii) the incorporation of small amounts of armored sulfide can thus account for the range of both [Os] and 187Os/188Os of EM-basalts worldwide without the need for contributions from additional silicate mantle reservoirs. References: [1] Zindler & Hart, (1986) Annu. Rev. Earth Planet. Sci. 14, 493-571. [2] Class et al. (2009) Earth Planet. Sci. Lett. 284, 219-227. [3] Stracke, et al. (2005) Geochem., Geophys., Geosys. 6, doi:10.1029/2004GC000824. [4] Burton et al., Earth Planet. Sci. Lett. (1999) 172, 311-322. [5] Alard et al., (2002) Earth Planet. Sci. Lett. 203, 651-663

Re-Os isotopic evidence for an enriched-mantle source for the Noril'sk-type, ore-bearing intrusions, Siberia

USGS Publications Warehouse

Walker, R.J.; Morgan, J.W.; Horan, M.F.; Czamanske, G.K.; Krogstad, E.J.; Fedorenko, V.A.; Kunilov, V.E.

1994-01-01

Magmatic Cu-Ni sulfide ores and spatially associated ultramafic and mafic rocks from the Noril'sk I, Talnakh, and Kharaelakh intrusions are examined for Re-Os isotopic systematics. Neodymium and lead isotopic data also are reported for the ultramafic and mafic rocks. The Re-Os data for most samples indicate closed-system behavior since the ca. 250 Ma igneous crystallization age of the intrusions. There are small but significant differences in the initial osmium isotopic compositions of samples from the three intrusions. Ores from the Noril'sk I intrusion have ??Os values that vary from +0.4 to +8.8, but average +5.8. Ores from the Talnakh intrusion have ??Os values that range from +6.7 to +8.2, averaging +7.7. Ores from the Kharaelakh intrusion have ??Os values that range from +7.8 to +12.9, with an average value of +10.4. The osmium isotopic compositions of the ore samples from the Main Kharaelakh orebody exhibit minimal overlap with those for the Noril'sk I and Talnakh intrusions, indicating that these Kharaelakh ores were derived from a more radiogenic source of osmium than the other ores. Combined osmium and lead data for major orebodies in the three intrusions plot in three distinct fields, indicating derivation of osmium and lead from at least three isotopically distinct sources. Some of the variation in lead isotopic compositions may be the result of minor lower-crustal contamination. However, in contrast to most other isotopic and trace element data, Os-Pb variations are generally inconsistent with significant crustal contamination or interaction with the subcontinental lithosphere. Thus, the osmium and lead isotopic compositions of these intrusions probably reflect quite closely the compositions of their mantle source, and suggest that these two isotope systems were insensitive to lithospheric interaction. Ultramafic and mafic rocks have osmium and lead isotopic compositions that range only slightly beyond the compositions of the ores. These rocks also have relatively uniform ??{lunate}Nd values that range only from -0.8 to + 1.1. This limited variation in neodymium isotopic composition may reflect the characteristics of the mantle sources of the rocks, or it may indicate that somehow similar proportions of crust contaminated the parental melts. The osmium, lead, and neodymium isotopic data for these rocks most closely resemble the mantle sources of certain ocean island basalts (OIB), such as some Hawaiian basalts. Hence, these data are consistent with derivation of primary melts from a mantle source similar to that of some types of hotspot activity. The long-term Re/Os enrichment of this and similar mantle sources, relative to chondritic upper mantle, may reflect 1. (1) incorporation of recycled oceanic crust into the source more than 1 Ga ago, 2. (2) derivation from a mantle plume that originated at the outer core-lower mantle interface, or 3. (3) persistence of primordial stratification of rhenium and osmium in the mantle. ?? 1994.

Experimental constraints on the fate of subducted upper continental crust beyond the "depth of no return"

NASA Astrophysics Data System (ADS)

Zhang, Yanfei; Wu, Yao; Wang, Chao; Zhu, Lüyun; Jin, Zhenmin

2016-08-01

The subducted continental crust material will be gravitationally trapped in the deep mantle after having been transported to depths of greater than ∼250-300 km (the "depth of no return"). However, little is known about the status of this trapped continental material as well as its contribution to the mantle heterogeneity after achieving thermal equilibrium with the surrounding mantle. Here, we conduct an experimental study over pressure and temperature ranges of 9-16 GPa and 1300-1800 °C to constrain the fate of these trapped upper continental crust (UCC). The experimental results show that partial melting will occur in the subducted UCC along normal mantle geotherm to produce K-rich melt. The residual phases composed of coesite/stishovite + clinopyroxene + kyanite in the upper mantle, and stishovite + clinopyroxene + K-hollandite + garnet + CAS-phase in the mantle transition zone (MTZ), respectively. The residual phases achieve densities greater than the surrounding mantle, which provides a driving force for descent across the 410-km seismic discontinuity into the MTZ. However, this density relationship is reversed at the base of the MTZ, leaving the descended residues to be accumulated above the 660-km seismic discontinuity and may contribute to the "second continent". The melt is ∼0.6-0.7 g/cm3 less dense than the surrounding mantle, which provides a buoyancy force for ascent of melt to shallow depths. The ascending melt, which preserves a significant portion of the bulk-rock rare earth elements (REEs), large ion lithophile elements (LILEs), and high-filed strength elements (HFSEs), may react with the surrounding mantle. Re-melting of the metasomatized mantle may contribute to the origin of the "enriched mantle sources" (EM-sources). Therefore, the deep subducted continental crust may create geochemical/geophysical heterogeneity in Earth's interior through subduction, stagnation, partial melting and melt segregation.

Genetic link between EMI and EMII: An adakite connection

NASA Astrophysics Data System (ADS)

Shimoda, Gen

2009-10-01

Geochemical modeling of the origin of enriched mantle I (EMI) and enriched mantle II (EMII) is conducted from the perspective of adakite production. For the model, the average composition of adakites is re-estimated from published data for eighteen trace elements. Although the concentrations determined for highly incompatible elements are very high (about 100 times of primitive mantle), these high concentrations can be explained by melting of oceanic crust without sediment contribution. The compiled data further suggest that the mantle-slab melt reaction would play a major role in the production of basic adakites. In addition, crystal fractionation in the magma chamber should produce additional chemical variations in adakites, in particular for acidic adakites. To examine the effect of chemical variations on the isotopic composition of recycled adakites, broad correlations between trace elements and SiO 2 concentrations, and the MELTS program are employed. The results suggest that recycling of a basic adakite (SiO 2 = 55%) can account for EMI isotopic signatures with storage times of about 2.0 Gyr. The isotopic compositions of less-basic adakites and their evolved magmas shift towards EMII values with increasing SiO 2 concentrations. In particular, evolved acidic adakite can yield EMII isotopic signatures. These lines of evidence suggest that the recycling of adakites at various stages of evolution can conceivably produce the entire isotopic range between EMI and EMII reservoirs. Consequently, adakite recycling via sediment subduction or subduction erosion can account for the origins of EMI and EMII reservoirs. In this context, residual garnet under high pressure and plagioclase fractionation at low pressure might play an essential role in producing the chemical variations among adakites that ultimately govern the isotopic compositions of these geochemical reservoirs.

Mesoarchean melting and Neoarchean to Paleoproterozoic metasomatism during the formation of the cratonic mantle keel beneath West Greenland

NASA Astrophysics Data System (ADS)

van Acken, D.; Luguet, A.; Pearson, D. G.; Nowell, G. M.; Fonseca, R. O. C.; Nagel, T. J.; Schulz, T.

2017-04-01

Highly siderophile element (HSE) concentration and 187Os/188Os isotopic heterogeneity has been observed on various scales in the Earth's mantle. Interaction of residual mantle peridotite with infiltrating melts has been suggested to overprint primary bulk rock HSE signatures originating from partial melting, contributing to the heterogeneity seen in the global peridotite database. Here we present a detailed study of harzburgitic xenolith 474527 from the Kangerlussuaq suite, West Greenland, coupling the Re-Os isotope geochemistry with petrography of both base metal sulfides (BMS) and silicates to assess the impact of overprint induced by melt-rock reaction on the Re-Os isotope system. Garnet harzburgite sample 474527 shows considerable heterogeneity in the composition of its major phases, most notably olivine and Cr-rich garnet, suggesting formation through multiple stages of partial melting and subsequent metasomatic events. The major BMS phases show a fairly homogeneous pentlandite-rich composition typical for BMS formed via metasomatic reaction, whereas the 187Os/188Os compositions determined for 17 of these BMS are extremely heterogeneous ranging between 0.1037 and 0.1981. Analyses by LA-ICP-MS reveal at least two populations of BMS grains characterized by contrasting HSE patterns. One type of pattern is strongly enriched in the more compatible HSE Os, Ir, and Ru over the typically incompatible Pt, Pd, and Re, while the other type shows moderate enrichment of the more incompatible HSE and has overall lower compatible HSE/incompatible HSE composition. The small-scale heterogeneity observed in these BMS highlights the need for caution when utilizing the Re-Os system to date mantle events, as even depleted harzburgite samples such as 474527 are likely to have experienced a complex history of metasomatic overprinting, with uncertain effects on the HSE.

Evidence of denser MgSiO3 glass above 133 gigapascal (GPa) and implications for remnants of ultradense silicate melt from a deep magma ocean.

PubMed

Murakami, Motohiko; Bass, Jay D

2011-10-18

Ultralow velocity zones are the largest seismic anomalies in the mantle, with 10-30% seismic velocity reduction observed in thin layers less than 20-40 km thick, just above the Earth's core-mantle boundary (CMB). The presence of silicate melts, possibly a remnant of a deep magma ocean in the early Earth, have been proposed to explain ultralow velocity zones. It is, however, still an open question as to whether such silicate melts are gravitationally stable at the pressure conditions above the CMB. Fe enrichment is usually invoked to explain why melts would remain at the CMB, but this has not been substantiated experimentally. Here we report in situ high-pressure acoustic velocity measurements that suggest a new transformation to a denser structure of MgSiO(3) glass at pressures close to those of the CMB. The result suggests that MgSiO(3) melt is likely to become denser than crystalline MgSiO(3) above the CMB. The presence of negatively buoyant and gravitationally stable silicate melts at the bottom of the mantle, would provide a mechanism for observed ultralow seismic velocities above the CMB without enrichment of Fe in the melt. An ultradense melt phase and its geochemical inventory would be isolated from overlying convective flow over geologic time.

Evidence of denser MgSiO3 glass above 133 gigapascal (GPa) and implications for remnants of ultradense silicate melt from a deep magma ocean

PubMed Central

Murakami, Motohiko; Bass, Jay D.

2011-01-01

Ultralow velocity zones are the largest seismic anomalies in the mantle, with 10–30% seismic velocity reduction observed in thin layers less than 20–40 km thick, just above the Earth’s core-mantle boundary (CMB). The presence of silicate melts, possibly a remnant of a deep magma ocean in the early Earth, have been proposed to explain ultralow velocity zones. It is, however, still an open question as to whether such silicate melts are gravitationally stable at the pressure conditions above the CMB. Fe enrichment is usually invoked to explain why melts would remain at the CMB, but this has not been substantiated experimentally. Here we report in situ high-pressure acoustic velocity measurements that suggest a new transformation to a denser structure of MgSiO3 glass at pressures close to those of the CMB. The result suggests that MgSiO3 melt is likely to become denser than crystalline MgSiO3 above the CMB. The presence of negatively buoyant and gravitationally stable silicate melts at the bottom of the mantle, would provide a mechanism for observed ultralow seismic velocities above the CMB without enrichment of Fe in the melt. An ultradense melt phase and its geochemical inventory would be isolated from overlying convective flow over geologic time. PMID:21969547

Not all Primordial Noble Gas Signatures are Associated with OIBs and Mantle Plumes - Mantle Heterogeneity, Primordial Shallow Sources and a Solar-like He, Ne Signature in an Ancient North American Craton

NASA Astrophysics Data System (ADS)

Ma, L.; Castro, M. C.; Hall, C. M.

2007-12-01

The presence of primordial He and Ne components in ocean island basalts (OIBs) as well as a mantle He/heat flux ratio lower than the production ratio near mid-ocean ridges have historically been used to support the existence of a two-layer mantle convection model. This would comprise a lower, primordial, undegassed reservoir from which He removal to the upper degassed mantle would be impeded. Arguments based on He and heat transport have been recently invalidated by Castro et al. (2005) and should no longer be used to justify the presence of two such distinct mantle reservoirs. Indeed, it was shown that such low He/heat flux ratios are expected and do not reflect a He deficit in the original crust or mantle reservoir. By contrast, the occurrence of a He/heat flux ratio greater than the radiogenic production ratio can only result from a past mantle thermal event in which the released heat has already escaped while the released He remains, and is slowly rising to the surface. Such a high He/heat flux ratio is present in shallow groundwaters of the Michigan Basin. We now present results of a new noble gas study conducted in the Michigan Basin, in which 38 deep (0.5-3.6km) brine samples were collected and analyzed for all noble gas abundances and isotopic ratios. As expected from previously computed shallow high He/heat flux ratios, both He and Ne isotopic ratios clearly indicate the presence of a mantle component. Of greater significance is the primordial, solar-like signature, of this mantle component. It is also the first primordial signature ever recorded in crustal fluids in a continental region. Because no hotspots or hotspot tracks are known in the area, it is highly unlikely for such primordial, solar-like signature to result from a mantle plume-related mechanism originating deep in the mantle. We argue that such a primordial signature can be explained by a shallow noble gas reservoir in the subcontinental lithospheric mantle (SCLM) beneath the Michigan Basin, possibly created by a mechanism similar to that proposed by Anderson (1998) for oceanic regions. Indeed, the Michigan Basin, located within the ancient North American craton (~1.1->2.5Ga), lies on a very thick U-Th depleted SCLM, possibly allowing preservation of a primordial, residual, mantle reservoir beneath the continental crust. Recent reactivation of the old mid-continent rift transecting the crystalline basement is likely responsible for the release of this primordial signature into the basin. The solar-like He and Ne signatures present in the Michigan Basin fluids not only suggest that a deep primordial mantle reservoir is not required to explain the presence of such components, they also point to a very heterogeneous mantle as previously suggested by Anderson (1998), Albarede (2005), and others. Consequently, the presence of a primordial noble gas signature, at least if observed in a continental region, should not be used to conclude at the existence of a deep mantle source and thus, of a hotspot as typically defined. The SCLM underneath ancient cratons is a great candidate for hosting primitive ancient mantle reservoirs. Arguments based on He/heat flux ratios as well as the presence of a primordial noble gas signature should not be used to support the existence of a lower, primordial, versus an upper, degassed mantle reservoir. Our study provides the first observational case for long-term primordial lithospheric storage. Anderson, 1998, Proc. Natl. Acad. Sci. USA, 95, 9087-9092. Albarede, 2005, AGU Monograph, 160, 27-46. Castro et al., 2005, EPSL, 237, 893-910.

Tracing subduction zone fluid-rock interactions using trace element and Mg-Sr-Nd isotopes

NASA Astrophysics Data System (ADS)

Wang, Shui-Jiong; Teng, Fang-Zhen; Li, Shu-Guang; Zhang, Li-Fei; Du, Jin-Xue; He, Yong-Sheng; Niu, Yaoling

2017-10-01

Slab-derived fluids play a key role in mass transfer and elemental/isotopic exchanges in subduction zones. The exhumation of deeply subducted crust is achieved via a subduction channel where fluids from various sources are abundant, and thus the chemical/isotopic compositions of these rocks could have been modified by subduction-zone fluid-rock interactions. Here, we investigate the Mg isotopic systematics of eclogites from southwestern Tianshan, in conjunction with major/trace element and Sr-Nd isotopes, to characterize the source and nature of fluids and to decipher how fluid-rock interactions in subduction channel might influence the Mg isotopic systematics of exhumed eclogites. The eclogites have high LILEs (especially Ba) and Pb, high initial 87Sr/86Sr (up to 0.7117; higher than that of coeval seawater), and varying Ni and Co (mostly lower than those of oceanic basalts), suggesting that these eclogites have interacted with metamorphic fluids mainly released from subducted sediments, with minor contributions from altered oceanic crust or altered abyssal peridotites. The positive correlation between 87Sr/86Sr and Pb* (an index of Pb enrichment; Pb* = 2*PbN/[CeN + PrN]), and the decoupling relationships and bidirectional patterns in 87Sr/86Sr-Rb/Sr, Pb*-Rb/Sr and Pb*-Ba/Pb spaces imply the presence of two compositionally different components for the fluids: one enriched in LILEs, and the other enriched in Pb and 87Sr/86Sr. The systematically heavier Mg isotopic compositions (δ26Mg = - 0.37 to + 0.26) relative to oceanic basalts (- 0.25 ± 0.07) and the roughly negative correlation of δ26Mg with MgO for the southwestern Tianshan eclogites, cannot be explained by inheritance of Mg isotopic signatures from ancient seafloor alteration or prograde metamorphism. Instead, the signatures are most likely produced by fluid-rock interactions during the exhumation of eclogites. The high Rb/Sr and Ba/Pb but low Pb* eclogites generally have high bulk-rock δ26Mg values, whereas high Pb* and 87Sr/86Sr eclogites have mantle-like δ26Mg values, suggesting that the two fluid components have diverse influences on the Mg isotopic systematics of these eclogites. The LILE-rich fluid component, possibly derived from mica-group minerals, contains a considerable amount of isotopically heavy Mg that has shifted the δ26Mg of the eclogites towards higher values. By contrast, the 87Sr/86Sr- and Pb-rich fluid component, most likely released from epidote-group minerals in metasediments, has little Mg so as not to modify the Mg isotopic composition of the eclogites. In addition, the influence of talc-derived fluid might be evident in a very few eclogites that have low Rb/Sr and Ba/Pb but slightly heavier Mg isotopic compositions. These findings represent an important step toward a broad understanding of the Mg isotope geochemistry in subduction zones, and contributing to understanding why island arc basalts have averagely heavier Mg isotopic compositions than the normal mantle.

Evidence of subduction and crust-mantle mixing from a single diamond

NASA Astrophysics Data System (ADS)

Schulze, Daniel J.; Harte, Ben; Valley, John W.; Channer, Dominic M. DeR.

2004-09-01

Cathodoluminescence (CL) imaging of polished sections of a diamond from the Guaniamo region of Venezuela suggests a history of the diamond involving two periods of growth separated by a period of resorption and possibly brittle deformation. In situ electron probe analysis of multiple eclogitic garnet inclusions reveals a correlation between garnet composition and location in the stone. An early-formed garnet in the diamond core has higher Ca/(Ca+Mg) and lower Mg/(Mg+Fe) values than later garnets associated with the second period of diamond growth. This variation conforms to an extensive trend of variation in the suite of eclogitic garnets extracted from Venezuelan diamonds. The diamond is zoned in carbon isotope composition (in situ secondary ion mass spectrometry, SIMS, data). The core compositions ( δ13C PDB), corresponding to the first stage of growth, average -17.7‰. The second period of growth is apparently in two sub-sets of CL zones with mean values of -13.0‰ and -7.9‰. Nitrogen contents of diamond are low (30-300 atomic ppm) and do not correlate with carbon isotope composition. Oxygen isotope ratios of the garnet inclusions are elevated substantially above those expected for "common mantle"; δ18O VSMOW of early garnet is approximately +10.5‰ and two late garnets average +8.8‰. The evolutionary trend of magnesium enrichment in garnet is unlikely to represent igneous fractionation. The stable isotope data are consistent with diamond formation in subducted meta-basic rocks that had interacted with sea water at low temperatures at or near the sea floor and contained a substantial biogenic carbon component. During or following subduction, diamonds continued to form in an evolving system that was progressively modified by interaction with mantle material.

Experimental constraints on metasomatism of mantle wedge peridotites by hybridized adakitic melts

NASA Astrophysics Data System (ADS)

Corgne, Alexandre; Schilling, Manuel E.; Grégoire, Michel; Langlade, Jessica

2018-05-01

In this study, a series of high-pressure (1.5 GPa) and high-temperature (1000-1300 °C) experiments were performed to investigate the petrological imprints of adakitic metasomatism on mantle wedge peridotites. Reaction couples were prepared using a powdered adakite from Cerro Pampa, Argentina (Mg# 0.7) placed in contact with a cored sample of medium-grained protogranular depleted spinel lherzolite from Pali Aike (Chile). Textural and chemical analyses of the run products allow us to identify key features of modal metasomatism by hybridized adakitic melts. The main changes in phase relations are associated with the following metasomatic reactions: incongruent dissolution of olivine and associated precipitation of secondary orthopyroxene, dissolution of primary spinel and subsequent replacement by secondary high-Cr spinel. In experiments with high water contents (9-12 wt%), precipitation of pargasitic amphibole also occurred, possibly at the expense of primary clinopyroxene. Neither phlogopite nor Ti-oxides were precipitated in any of these experiments. As expected, primary pyroxenes do not show evidence of being significantly altered following the interaction with the produced siliceous melts. Within the adakitic portion of the experimental charge, it was also observed the crystallization of secondary Ti-rich, Cr- and Na-poor diopsidic clinopyroxene, andesine plagioclase and, at low temperature, Fe-enriched secondary orthopyroxene. Considering textural criteria, we interpreted the formation of these minerals as crystallization products of the adakite component and not as true products of metasomatic reactions. The experimental results are used to discuss some of the petrological evidences presented to support modal metasomatism by slab-derived melts of mantle xenoliths extracted from several suprasubduction settings located around the Pacific Ring of Fire.

Mantle heterogeneities beneath the Northeast Indian Ocean as sampled by intra-plate volcanism at Christmas Island

NASA Astrophysics Data System (ADS)

Taneja, Rajat; Rushmer, Tracy; Blichert-Toft, Janne; Turner, Simon; O'Neill, Craig

2016-10-01

The intra-plate region of the Northeast Indian Ocean, located between the Ninetyeast Ridge and the North West Shelf of Australia, contains numerous submerged seamounts and two sub-aerially exposed volcanic island groups. While the Cocos (Keeling) Archipelago is a coral atoll, Christmas Island is the only sub-aerially exposed volcanic island and contains Late Cretaceous, Eocene and Pliocene lavas. The lavas are predominantly basaltic in composition, except for one sampled flow that is trachytic. Although the evolution of the western margin of Australia, and the seismicity in the intra-plate region, has received considerable attention, the origin of the seamount province in the Northeast Indian Ocean is still a matter of debate. In order to constrain the origin of volcanism on Christmas Island and the associated Seamount Province we analysed 14 Christmas Island samples for major and trace element abundances and 12 of these for Nd, Hf and Pb isotope compositions. The trace element patterns of the lavas are similar to many ocean island basalts, while high 208Pb/204Pb and 207Pb/204Pb at a given 206Pb/204Pb suggest affiliation with the DUPAL anomaly. The reconstructed position of Christmas Island during the Eocene (44-37 Ma) places the island in close proximity to the (present-day) upper mantle low-seismic velocity anomalies. Moreover, an enriched mantle (EM-2) type component in addition to the DUPAL anomaly is observed in the Eocene volcanic phase. The younger Pliocene ( 4 Ma) sequences at Christmas Island are inferred to be the product of partial melting of existing material induced by lithospheric flexure.

The Molybdenum Isotope System as a Tracer of Slab Input in Subduction Zones: An Example From Martinique, Lesser Antilles Arc

NASA Astrophysics Data System (ADS)

Gaschnig, Richard M.; Reinhard, Christopher T.; Planavsky, Noah J.; Wang, Xiangli; Asael, Dan; Chauvel, Catherine

2017-12-01

Molybdenum isotopes are fractionated by Earth-surface processes and may provide a tracer for the recycling of crustal material into the mantle. Here, we examined the Mo isotope composition of arc lavas from Martinique in the Lesser Antilles arc, along with Cretaceous and Cenozoic Deep Sea Drilling Project sediments representing potential sedimentary inputs into the subduction zone. Mo stable isotope composition (defined as δ98Mo in ‰ deviation from the NIST 3134 standard) in lavas older than ˜7 million years (Ma) exhibits a narrow range similar to and slightly higher than MORB, whereas those younger than ˜7 Ma show a much greater range and extend to unusually low δ98Mo values. Sediments from DSDP Leg 78A, Site 543 have uniformly low δ98Mo values whereas Leg 14, Site 144 contains both sediments with isotopically light Mo and Mo-enriched black shales with isotopically heavy Mo. When coupled with published radiogenic isotope data, Mo isotope systematics of the lavas can be explained through binary mixing between a MORB-like end-member and different sedimentary compositions identified in the DSDP cores. The lavas older than ˜7 Ma were influenced by incorporation of isotopically heavy black shales into the mantle wedge. The younger lavas are the product of mixing isotopically light sedimentary material into the mantle wedge. The change in Mo isotope composition of the lavas at ˜7 Ma is interpreted to reflect the removal of the Cretaceous black shale component due to the arrival of younger ocean crust where the age-equivalent Cretaceous sediments were deposited in shallower oxic waters. Isotopic fractionation of Mo during its removal from the slab is not required to explain the observed systematics in this system.

Mantle xenoliths from Marosticano area (Northern Italy): a comparison with Veneto Volcanic Province lithospheric mantle

NASA Astrophysics Data System (ADS)

Brombin, Valentina; Bonadiman, Costanza; Coltorti, Massimo

2016-04-01

The Tertiary Magmatic Province of Veneto, known as Veneto Volcanic Province (VVP), in the North-East of Italy, represents the most important volcanic distric of Adria Plate. It is composed by five volcanic bodies: Val d'Adige, Marosticano, Mts. Lessini, Berici Hills and Euganean Hills. Most of the volcanic products are relatively undifferentiated lavas and range in composition from nephelinites to tholeiites. Often VVP nephelinites and basanites carry mantle xenoliths (mainly harzburgites and lherzolite). This study reports petrological comparison between Marosticano xenoliths (new outcrop) and xenoliths from the Lessinean and Val d'Adige areas already studied by many Authors (Siena & Coltorti 1989; Beccaluva et al., 2001, Gasperini et al., 2006). Mineral major elements analyses show that the Marosticano lherzolites and harzburgites reflect "more restitic" composition than the mantle domain beneath the other VVP districts (Lessini Mts. and Val d'Adige). In fact, olivine and pyroxene of Marosticano xenoliths have the highest mg# values of the entire district (Marosticano→90-93; literature→86-92). At comparable mg# (45-85 wt%) Marosticano spinels tend to be higher in Cr2O3 (23-44 wt%) contents with respect to the other VVP sp (7-25 wt%). It is worth noting that, Ni contents of Marosticano olivines in both harzburgites and lherzolites are higher (2650-3620 ppm) than those of the Lessinean xenoliths (1500- 3450 ppm), and similar to that of Val d'Adige lherzolites (3000-3500 ppm), approaching the contents of Archean cratonic mantle (Kelemen, 1998). In turn, Lessinean olivines properly fall in the Ni-mg# Phanerozoic field. At fixed pressure of 15 kbar, the equilibration temperature of Marosticano xenoliths are similar (Brey & Köhler: 920-1120°C) to those of Lessini (O'Neill & Wall: 990-1110°C; Beccaluva et al., 2007), but higher than those of Val d'Adige (Wells: 909-956°C; Gasperini et al., 2006). Finally, Marosticano mantle fragment show similar relatively high redox conditions (Δlog fO2: +1.2 to -0.7, Ballhaus, 1991) to Lessinean and Val d'Adige xenoliths which may indicate a local oxidation of the mantle below this portion of VVP. References • Beccaluva L., Bianchini G., Bonadiman C., Coltorti M., Milani L., Salvini L., Siena F., Tassinari R. (2007). Intraplate lithospheric and sublithospheric components in the Adriatic domain: Nephelinite to tholeiite magma generation in the Paleogene Veneto Volcanic Province, Southern Alps. Geological Society of America, 131-152. • Beccaluva L., Bonadiman C., Coltorti M., Salvini L., Siena F. (2001). Depletion events, nature of metasomatizing agent and timing of enrichment processes in lithospheric mantle xenoliths from the Veneto Volcanic Province. Journal of Petrology, 42, 173-187. • Gasperini D., Bosch D., Braga R., Bondi M., Macera P., Morten L. (2006). Ultramafic xenoliths from the Veneto Volcanic Province (Italy): Petrological and geochemical evidence for multiple metasomatism of the SE Alps mantle lithospere. Geochemical Journal, 40, 377-404. • Siena F., Coltorti M. (1989). Lithospheric mantle evolution: evidences from ultramafic xenoliths in the Lessinean volcanics (Northern Itlay). Chemical Geology, 77, 347-364.

Symplectite in spinel lherzolite xenoliths from the Little Hungarian Plain, Western Hungary: A key for understanding the complex history of the upper mantle of the Pannonian Basin

NASA Astrophysics Data System (ADS)

Falus, György; Szabó, Csaba; Kovács, István; Zajacz, Zoltán; Halter, Werner

2007-03-01

Two spinel lherzolite xenoliths from Hungary that contain pyroxene-spinel symplectites have been studied using EPMA, Laser ablation ICP-MS and universal stage. Based on their geochemical and structural characteristics, the xenoliths represent two different domains of the shallow subcontinental lithospheric mantle beneath the Pannonian Basin. The occurrence of symplectites is attributed to the former presence and subsequent breakdown of garnets due to significant pressure decrease related to lithospheric thinning. This implies that both mantle domains were once part of the garnet lherzolitic upper mantle and had a similar history during the major extension that formed the Pannonian Basin. Garnet breakdown resulted in distinct geochemical characteristics in the adjacent clinopyroxene crystals in both xenoliths. This is manifested by enrichment in HREE, Y, Zr and Hf towards the clinopyroxene porphyroclast rims and also in the neoblasts with respect to porphyroclast core compositions. This geochemical feature, together with the development and preservation of the texturally very sensitive symplectites, enables us to determine the relative timing of mantle processes. Our results indicate that garnets had been metastable in the spinel lherzolite environment and their breakdown to pyroxene and spinel is one of the latest processes that took place within the upper mantle before the xenoliths were brought to the surface.

Thallium as a tracer of fluid-rock interaction in the shallow Mariana forearc

NASA Astrophysics Data System (ADS)

Nielsen, Sune G.; Klein, Frieder; Kading, Tristan; Blusztajn, Jerzy; Wickham, Katie

2015-11-01

Fluids driven off the subducting Pacific plate infiltrate the shallow Mariana forearc and lead to extensive serpentinization of mantle peridotite. However, the sources, pathways, and chemical modifications of ascending, slab-derived fluids remain poorly constrained and controversial. In this study, we use thallium (Tl) concentrations and isotopic ratios of serpentinized peridotite and rodingitized diabase from the South Chamorro and Conical Seamounts to discriminate between potential fluid sources with distinct Tl isotope compositions. Serpentinite samples from the Mariana forearc all display ε205 Tl > - 0.5 (where ε205 Tl = 10 , 000 × (205Tl /Tl203sample -205Tl /SRM 997 203Tl ) / (205Tl / SRM 997 203Tl )), which is significantly enriched in 205Tl compared to the normal mantle (ε205 Tl = - 2). Given that high temperature hydrothermal processes do not impart significant Tl isotope fractionation, the isotope compositions of the serpentinites must reflect that of the serpentinizing fluid. Pelagic sediments are the only known slab component that consistently displays ε205 Tl > - 0.5 and, therefore, we interpret the heavy Tl isotope signatures as signifying that the serpentinizing fluids were derived from subducting pelagic sediments. A rodingitized diabase from Conical Seamount was found to have an ε205 Tl of 0.8, suggesting that sediment-sourced serpentinization fluids could also affect diabase and other mafic lithologies in the shallow Mariana forearc. Forearc rodingitization of diabase led to a strong depletion in Tl content and a virtually complete loss of K, Na and Rb. The chemical composition of hybrid fluids resulting from serpentinization of harzburgite with concomitant rodingitization of diabase can be highly alkaline, depleted in Si, yet enriched in Ca, Na, K, and Rb, which is consistent with the composition of fluids emanating from mud volcanoes in the Mariana forearc. Our study suggests that fluid-rock interactions between sedimentary, mafic, and ultramafic lithologies are strongly interconnected even in the shallowest parts of subduction zones. We conclude that transfer of fluids and dissolved elements at temperatures and pressures below 400 °C and 1 GPa, respectively, must be taken into account when elemental budgets and mass transfer between the subducting plate, the forearc, the deep mantle and the ocean are evaluated.

Geologically Controlled Isotope-Time Patterns Reveal Early Differentiation and Crust Formation Processes

NASA Astrophysics Data System (ADS)

Bennett, V. C.; Nutman, A. P.

2014-12-01

The mechanisms of continental crust production and evolution in the early Earth remain controversial, as are questions of the relative roles of early differentiation versus subsequent tectonic procssing in creating Earth's chemical signatures. Here we present geologic observations integrated with whole rock major, trace element and Sm-Nd isotopic signatures and combined with U-Pb and Lu-Hf isotopic compositions of zircon populations from the same rocks, from the most extensive early rock record comprising the 3.9 Ga to 3.6 Ga terranes of southwest Greenland. These data reveal repeated patterns of formation of juvenile TTG crust and associated mafic and ultramafic rocks in convergent margin settings followed by formation of more evolved granites [1]. Our new zircon Lu-Hf data from rare 3.6-3.7 Ga tonalites within the Itsaq Gneiss Complex, obtained from single component, non-migmatitic gneisses with simple zircon populations, limited within sample Hf isotopic variability and accurate U-Pb ages, now document extraction of juvenile tonalites from a near chondritic mantle source between 3.9 Ga and 3.6 Ga. The more evolved, granitic rocks in each area show slightly negative initial ɛHf in accord with crustal reworking of the older (3.8-3.9 Ga) gniesses. There is no evidence for Hadean material in the sources of the granitoids. The Hf isotope-time patterns are consistent with juvenile crust production from a mantle source that experienced only modest amounts of prior crustal extraction. They are distinct from those predicted by reprocessing of an enriched Hadean mafic crust, as has been proposed for this region [2] and for the source of the Hadean Jack Hills zircons [3]. The well-documented, time decreasing, positive 142Nd anomalies [e.g., 4] from these rocks are further evidence of crustal derivation from a convecting mantle source, rather than reworking of an enriched mafic lithosphere. The 143Nd isotopic -time patterns are more complex, reflecting the interplay between early Sm/Nd fractionation processes as required by the 142Nd data, juvenile crustal growth and in some cases geologic disturbance of the whole rock Sm-Nd system. [1] Nutman, et al, (2013) Amer. Jour. Sci. 313, 877-911. [2] Naeraa et al.. (2012) Nature 485, 627-631. [3] Kemp et al., (2010) EPSL 296, 45-56. [4] Bennett et al., (20070 Science 318, 1907.

Geochemistry of serpentinites in subduction zones: A review

NASA Astrophysics Data System (ADS)

Deschamps, Fabien; Godard, Marguerite; Guillot, Stéphane; Hattori, Kéiko

2013-04-01

Over the last decades, numerous studies have emphasized the role of serpentinites in the subduction zones geodynamics. Their presence and effective role in this environment is acknowledged notably by geophysical, geochemical and field observations of (paleo-) subduction zones. In this context, with the increasing amount of studies concerning serpentinites in subduction environments, a huge geochemical database was created. Here, we present a review of the geochemistry of serpentinites, based on the compilation of ~ 900 geochemical analyses of abyssal, mantle wedge and subducted serpentinites. The aim was to better understand the geochemical evolution of these rocks during their subduction history as well as their impact in the global geochemical cycle. When studying serpentinites, it is often a challenge to determine the nature of the protolith and their geological history before serpentinisation. The present-day (increasing) geochemical database for serpentinites indicates little to no mobility of incompatible elements at the scale of the hand-sample in most serpentinized peridotites. Thus, Rare Earth Elements (REE) distribution can be used to identify the initial protolith for abyssal and mantle wedge serpentinites, as well as magmatic processes such as melt/rock interactions taking place before serpentinisation. In the case of subducted serpentinites, the interpretation of trace element data is more difficult due to secondary enrichments independent of the nature of the protolith, notably in (L)REE. We propose that these enrichments reflect complex interactions probably not related to serpentinisation itself, but mostly to fluid/rock or sediment/rock interactions within the subduction channel, as well as intrinsic feature of the mantle protolith which could derive from the continental lithosphere exhumed at the ocean-continent transition. Additionally, during the last ten years, numerous studies have been carried out, notably using in situ approaches, to better constrain the geochemical budget of fluid-mobile elements (FME; e.g. B, Li, Cl, As, Sb, U, Th, Sr) stored in serpentinites and serpentine phases. These elements are good markers of the fluid/rock interactions taking place during serpentinisation. Today, the control of serpentinites on the behaviour of these elements, from their incorporation to their gradually release during subduction, is better understood. Serpentinites must be considered as a component of the FME budget in subduction zones and their role, notably on arc magmas composition, is undoubtedly underestimated presently in the global geochemical cycle.

Noble gases in submarine pillow basalt glasses from Loihi and Kilauea, Hawaii: A solar component in the Earth

DOE Office of Scientific and Technical Information (OSTI.GOV)

Honda, M.; McDougall, I.; Patterson, D.B.

1993-02-01

Noble gas elemental and isotopic abundances have been analysed in twenty-two samples of basaltic glass dredged from the submarine flanks of two currently active Hawaiian volcanoes, Loihi Seamount and Kilauea. Neon isotopic ratios are enriched in [sup 20]Ne and [sup 21]Ne by as much as 16% with respect to atmospheric ratios. All the Hawaiian basalt glass samples show relatively high [sup 3]He/[sup 4]He ratios. The high [sup 20]Ne/[sup 22]Ne values in some of the Hawaiian samples, together with correlations between neon and helium systematics, suggest the presence of a solar component in the source regions of the Hawaiian mantle plume.more » The solar hypothesis for the Earth's primordial noble gas composition can account for helium and neon isotopic ratios observed in basaltic glasses from both plume and spreading systems, in fluids in continental hydrothermal systems, in CO[sub 2] well gases, and in ancient diamonds. These results provide new insights into the origin and evolution of the Earth's atmosphere.« less

The behavior and concentration of CO2 in the suboceanic mantle: Inferences from undegassed ocean ridge and ocean island basalts

NASA Astrophysics Data System (ADS)

Michael, Peter J.; Graham, David W.

2015-11-01

In order to better determine the behavior of CO2 relative to incompatible elements, and improve the accuracy of mantle CO2 concentration and flux estimates, we determined CO2 glass and vesicle concentrations, plus trace element contents for fifty-one ultradepleted mid-ocean ridge basalt (MORB) glasses from the global mid-ocean ridge system. Fifteen contained no vesicles and were volatile undersaturated for their depth of eruption. Thirty-six contained vesicles and/or were slightly oversaturated, and so may not have retained all of their CO2. If this latter group lost some bubbles during emplacement, then CO2/Ba calculated for the undersaturated group alone is the most reliable and uniform ratio at 98 ± 10, and CO2/Nb is 283 ± 32. If the oversaturated MORBs did not lose bubbles, then CO2/Nb is the most uniform ratio within the entire suite of ultradepleted MORBs at 291 ± 132, while CO2/Ba decreases with increasing incompatible element enrichment. Additional constraints on CO2/Ba and CO2/Nb ratios are provided by published estimates of CO2 contents in highly vesicular enriched basalts that may have retained their vesicles e.g., the Mid-Atlantic Ridge "popping rocks", and from olivine-hosted melt inclusions in normal MORBs. As incompatible element enrichment increases, CO2/Nb increases progressively from 283 ± 32 in ultradepleted MORBs to 603 ± 69 in depleted melt inclusions to 936 ± 132 in enriched, vesicular basalts. In contrast, CO2/Ba is nearly uniform in these sample suites at 98 ± 10, 106 ± 24 and 111 ± 11 respectively. This suggests that Ba is the best proxy for estimating CO2 contents of MORBs, with an overall average CO2/Ba = 105 ± 9. Atlantic, Pacific and Indian basalts have similar values. Gakkel Ridge has lower CO2/Ba because of anomalously high Ba, and is not included in our global averages. Using the CO2/Ba ratio and published compilations of trace elements in average MORBs, the CO2 concentration of a primary, average MORB is 2085+ 473/- 427 ppm, while primary NMORB magmas (> 500 km from ocean island hotspots) have 1840 ppm CO2. The annual flux of CO2 from mid-ocean ridges is 1.25 ± 0.16 × 1014 g/yr, with possible values as low as 0.93 and as high as 1.61 × 1014 g/yr. This amount is equivalent to approximately 0.3% of the anthropogenic addition of CO2 to Earth's atmosphere. NMORB mantle has 183 ppm CO2 (50 ppm C) based on simple melting models and 13% melting. More realistic estimates of incompatible element concentrations in the depleted mantle that are consistent with complex melting models yield much lower estimates for CO2 in the depleted mantle: around 60-130 ppm CO2, with large uncertainties that are more related to melting models than to CO2/Ba. CO2/Ba is not correlated with isotopic or trace element ratios, but there may be systematic regional mantle variations. Iceland melt inclusions and Gakkel Ridge MORBs have lower CO2/Ba ratios, showing that these regional high Ba anomalies are not accompanied by correspondingly high CO2 concentrations.

Geochemistry and mineralogy of kimberlites from the Arkhangelsk Region, NW Russia: evidence for transitional kimberlite magma types

NASA Astrophysics Data System (ADS)

Beard, A. D.; Downes, H.; Hegner, E.; Sablukov, S. M.

2000-03-01

The Arkhangelsk kimberlite province (AKP) is situated in the north of the Baltic Shield within the buried southeastern portion of the Kola-Kuloi craton. It forms part of the extensive Devonian magmatic event of the northern Baltic Shield and Kola Peninsula. Two main groups of kimberlites can be distinguished within the province: (1) kimberlites from the diamondiferous Zolotitsa field that have geochemical and isotopic affinities with Group 2 kimberlites and lamproites; (2) diamond-poor Ti-Fe-rich kimberlites from other Arkhangelsk fields that have geochemical and isotopic affinities with Group 1 kimberlites. However, the Zolotitsa and Ti-Fe-rich kimberlites have mineralogical characteristics that are not typical for their respective assigned kimberlite group classifications. Both groups of Arkhangelsk kimberlites are apparently transitional to Group 1 kimberlites, Group 2 kimberlites and lamproites as they are defined elsewhere in the world. An associated kimberlite from the Mela Sill Complex has strong affinities with carbonatites. The low Al 2O 3, high Ni and Cr contents, and high Mg# in both groups of kimberlites indicate strongly depleted lherzolitic-harzburgitic mantle sources. Trace element patterns show a variable enrichment of incompatible elements and strong LREE enrichment. However, kimberlites from the Zolotitsa field have overall lower trace element abundances and less steep REE patterns, suggesting a higher degree of partial melt and/or a less enriched source compared to that of the Ti-Fe-rich kimberlites. A calciocarbonatite of the Mela Sill Complex has trace element and REE patterns typical of other carbonatites closely associated with kimberlites. 87Sr/ 86Sri and 143Nd/ 144Ndi isotope compositions of the Arkhangelsk kimberlites and carbonatite reveal that at least two mantle sources are required to explain the isotopic variation: (1) most of the Zolotitsa and Mela kimberlites and the Mela carbonatite are derived from an ancient enriched lithospheric source (EMI); (2) the Ti-Fe-rich kimberlites are derived from a plume-related asthenospheric mantle source with an isotopic composition close to Bulk Earth. Present-day Pb isotope compositions reveal that the Zolotitsa kimberlites have values close to Group 1 kimberlites. However, the Ti-Fe-rich kimberlites generally have slightly more radiogenic Pb isotope values.

NiO and Fe/Mn in Fo-rich olivines from OIB, MORB, and mantle peridotites

NASA Astrophysics Data System (ADS)

Li, H.; Baker, M.; Hofmann, A. E.; Clague, D.; Stolper, E.

2006-12-01

Olivines from mantle peridotites have a narrow range of NiO (0.36±0.03 [1σ] wt%), but NiO of olivines in basalts suggest NiO in mantle olivines is actually more variable: e.g., Hawaiian phenocrysts (Fo>90) have NiO >0.55%, and olivines from continental flood basalts can have >0.5% NiO. At the other end of the spectrum, some basaltic suites (e.g., Iceland, MORBs) have Fo>90 olivines with NiO >0.2%. Partial melting calculations on peridotites show it is difficult to generate liquids that crystallize Fo>90 olivines with >0.4% NiO without resorting to complex processes. Hypotheses to explain the variability of NiO in mantle-derived olivines include (1) reaction of peridotite with silica-rich melts of eclogite results in decreasing modal abundance of olivine and increasing NiO in olivine [1,2]; (2) magmas with NiO-rich olivines come from sources enriched in NiO due to a core-derived component [3]. [4] proposed that high Fe/Mn of Hawaiian vs. Icelandic and MORB lavas reflect a core-derived component in their sources. Possible core incorporation is poorly constrained but FeO and NiO are expected to increase by such processes, leading to correlations between NiO and Fe/Mn in mantle rocks with significant core-derived components. We present high-precision analyses of Fo-rich olivines from OIBs, MORBs, komatiites, and mantle peridotites, focusing on NiO contents and Fe/Mn ratios. Our goal is to test hypotheses to explain elevated NiO of Fo-rich olivines in basalts. Olivines are Fo85.1-93.4; more were analyzed, but we focused on this range to avoid complications due to decreasing NiO in olivine with crystallization. Errors (1σ) are 0.01 wt% in NiO and 1.5 in Fe/Mn (wt). Our data show several features: (1) NiO contents and Fe/Mn ratios of Fo>88 olivines are positively correlated, with the low end of the trend (NiO ~0.23%, Fe/Mn ~61) defined by MORB and Iceland and the high end of the trend (NiO ~0.55%, Fe/Mn ~80) by Reunion and Hawaii. Between these end points, there is a regular trend from MORB/Iceland, to Baffin Isl, to mantle peridotites/Juan Fernandez, to Reunion/Hawaii. This array can't be explained by simple crystallization (all have similar Fo) or by variable degrees of partial melting of a single source. The NiO-Fe/Mn correlation can be modeled by quantitative addition of 1-2% oxidized core to depleted mantle and thus is consistent with the core-addition hypothesis. However, more complex core-mantle interactions/fractionations would still be required to explain trace siderophile and chalcophile elements and isotopes. Moreover, other hypotheses to explain the observed trend (including addition of silicic melts to peridotite) cannot be ruled out. (2) The Hawaiian data, although clearly defining with Reunion the upper end of the overall NiO-Fe/Mn array, are more complex. For example, a single Mauna Kea sample has ~Fo90 phenocrysts with NiO from 0.30 to 0.54%, all with Fe/Mn=72-80, and North Arch and Loihi olivines have relatively low NiO at Fe/Mn ratios comparable to other Hawaiian olivines. Although Loihi and North Arch lavas are low in SiO2, in detail the NiO of Hawaiian olivines are not well predicted by SiO2 contents of the host lavas. (3) The Gorgona Isl komatiites fall off the overall trend, extending to NiO >0.5 wt% at Fe/Mn ~62, perhaps reflecting different sources, processes, or anomalous degrees of melting. [1] Kelemen et al (1998) EPSL 164, 387-406 [2] Sobolev et al (2005) Nature 434, 590-597 [3] Ryabchikov (2003) Doklady Earth Sci. 389A, 437-439 [4] Humayun et al (2004) Science 306, 91-94

Mantle Flow Induced by Subduction Beneath Taurides Mountains

NASA Astrophysics Data System (ADS)

Hui, H.; Sandvol, E. A.; Rey, P. F.; Brocard, G. Y.

2017-12-01

GPS data of Anatolian Plateau shows westward plate motion with respect to the Eurasian plate at a rate of approximately 20 mm/yr, however, the fast direction of shear-wave splitting data in Anatolian Plateau is dominantly northeast-southwest, with significant variations around the central Taurides Mountains. To address the decoupling between the deformation in the crust and in the mantle, we explore the mantle strain pattern beneath Anatoian Plateau. Numerical models of the African plate subducting beneath the Taurides have been constructed with the open source code Underworld by Louis Moresi and the Lithospheric Modeling Recipe by EarthByte Group. We have constructed a 2-D model with dimension of 400km × 480km with 60km thick plate subducting into the mantle. In our numerical model, we observe a poloidal component of the mantle flow around the edge of the subducting plate, which could be explained by straight-forward corner flow. The horizontal component of mantle flow above the subducting plate may explain the shear-wave splitting pattern that is nearly perpendicular to the trench at Anatolia. We are also working on 3-D models with dimension of 400km×400km×480km with the subducting plate width 100km. The asthenospheric mantle below the subducting plate exhibits a flow parallel to the trench, then rotates around the edge of the plate and becomes perpendicular to the trench. This mantle flow pattern may explain the shear-wave splitting directions in central Anatolia.

Anorthite: Thermal equation of state to high pressures. [for comparison with Earth interior and cratering properties of lunar surface

NASA Technical Reports Server (NTRS)

Jeanloz, R.; Ahrens, T. J.

1979-01-01

The shock wave (Hugoniot) data on single crystal and porous anorthite (CaAl2Si208) to pressures of 120 GPa are presented. These data are inverted to yield high pressure values of the Grueneisen parameter, adiabatic bulk modulus, and coefficient of thermal expansion over a broad range of pressures and temperatures which in turn are used to reduce the raw Hugoniot data and construct an experimentally based, high pressure thermal equation of state for anorthite. The hypothesis that higher order anharmonic contributions to the thermal properties decrease more rapidly upon compression than the lowest order anharmonicities is supported. The properties of anorthite corrected to lower mantle conditions show that although the density of anorthite is comparable to that of the lower most mantle, its bulk modulus is considerably less, hence making enrichment in the mantle implausible except perhaps near its base.

A colossal impact enriched Mars' mantle with noble metals

NASA Astrophysics Data System (ADS)

Brasser, R.; Mojzsis, S. J.

2017-06-01

Once the terrestrial planets had mostly completed their assembly, bombardment continued by planetesimals left over from accretion. Highly siderophile element (HSE) abundances in Mars' mantle imply that its late accretion supplement was 0.8 wt %; Earth and the Moon obtained an additional 0.7 wt % and 0.02 wt %, respectively. The disproportionately high Earth/Moon accretion ratio is explicable by stochastic addition of a few remaining Ceres-sized bodies that preferentially targeted Earth. Here we show that Mars' late accretion budget also requires a colossal impact, a plausible visible remnant of which is the emispheric dichotomy. The addition of sufficient HSEs to the Martian mantle entails an impactor of at least 1200 km in diameter to have struck Mars before 4430 Ma, by which time crust formation was well underway. Thus, the dichotomy could be one of the oldest geophysical features of the Martian crust. Ejected debris could be the source material for its satellites.

Geochemical constraints on the origin of serpentinization of oceanic mantle

NASA Astrophysics Data System (ADS)

Li, Z.; Lee, C. A.

2004-12-01

The lower seismic zone of double seismic zones in subducting oceanic lithosphere is suggested to be a result of serpentine or chlorite dehydration in the lithospheric mantle (Hacker et al., 2003). However, the mechanism by which oceanic lithospheric mantle is serpentinized is unclear. One way is through hydrothermal circulation where the lithospheric mantle represents part of the circuit through which seawater passes and then returns to the ocean. Another way is to inject seawater into the lithospheric mantle through fractures in the overlying crust without having a return path of water to the ocean. The two mechanisms differ in that the former is an open system process whereas the latter is a closed system process in which the mantle serves as a ¡°sponge¡± for water. Identifying the dominant process is important. For example, if the mantle is part of a hydrothermal circulation cell, the interaction of seawater with the mantle will influence the composition of seawater. This also has important implications for the heat flow out of seafloor. On the other hand, if serpentinization occurs by a closed system process, there will be no influence on seawater composition. Previous studies have suggested that serpentinization of ophiolite bodies was an isochemical process, hence closed system, but it was not clear in these studies whether serpentinization occurred in situ in the oceanic lithosphere. To better understand serpentinization processes in the oceanic lithosphere, we investigated a continuous transition zone of relatively unaltered harzburgite to completely serpentinized harzburgite in the Feather River Ophiolite in northern California. These samples are highly enriched in Na, K, Rb, Cs, U, and Sr, which strongly suggests that serpentinization occurred while the oceanic lithosphere was beneath the ocean. All samples (n=19) have Al2O3 contents ranging from 0.6 to 2.5 wt.% and have extremely depleted light rare-earth element abundances, indicating that these samples are cpx-free harzburgites, which have experienced roughly 20 to 35% melt extraction. The degree of serpentinization was quantified using the concentration of magnetite, a by-product of serpentinization. The lack of antigorite suggests that serpentinization occurred at temperatures lower than 300 C. By comparing Cr and Cr/Al systematics to that predicted from theoretical partial melting calculations and empirical relationships in unaltered peridotite xenoliths, it is shown that Cr and Al are immobile. Al content was thus used to determine the composition of the protolith, which allows us to estimate the amount of depletion/enrichment of a given element by processes other than melt depletion. Most of the harzburgites show no evidence for mantle metasomatism as evidenced by extreme depletions in LREE elements. Consistent with previous studies, we find no depletions in Mg, Fe, or Ca. As seawater is undersaturated in Mg-bearing minerals, an open system process would yield progressive depletion of Mg as is seen in abyssal peridotites, which have been weathered by seawater at the bottom of the seafloor (e.g., Snow et al. 1995). Collectively, this suggests that, except for the addition of seawater and its constituents, serpentinization of the Feather River Ophiolite, was a closed system process. By combining these observations with the results of our field mapping project, we suggest that serpentinization of the lithospheric mantle occurs by local introduction of seawater through fractures extending from the crust and into the mantle. We find no evidence that serpentinized zones in oceanic lithospheric mantle represents an extremely deep hydrothermal circulation cell.

He, Ne and Ar systematics in single vesicles: Mantle isotopic ratios and origin of the air component in basaltic glasses

NASA Astrophysics Data System (ADS)

Raquin, Aude; Moreira, Manuel Alexis; Guillon, Fabien

2008-09-01

An outstanding problem in understanding the origin of the gaseous phase, particularly the rare gas compositions in magmatic rocks, is the ubiquitous atmospheric component in bulk rock samples, and whether this atmospheric component is a late stage contamination of the sample, or a recycled component though sediments or altered oceanic crust. In the present study we address this problem by analyzing single vesicles from the "popping rock 2∏D43" sample from the Mid-Atlantic Ridge using a UV laser ablation system. We have determined both elemental and isotopic compositions of He, Ne and Ar in single vesicles as well as Kr and Xe abundances. All vesicles analyzed have an isotopic composition identical to the referred degassed mantle value estimated from this same sample, despite analyzing vesicles from a wide size distribution. The atmospheric component, which is always detected in bulk samples by crushing or heating, was not detected in the single vesicles. This implies that the recycling of atmospheric noble gases in the mantle cannot explain the air-like component of this sample. The addition of the atmospheric component must occur either during the eruption, or after sample recovery.

The longevity of Archean mantle residues in the convecting upper mantle and their role in young continent formation

NASA Astrophysics Data System (ADS)

Liu, Jingao; Scott, James M.; Martin, Candace E.; Pearson, D. Graham

2015-08-01

The role played by ancient melt-depleted lithospheric mantle in preserving continental crust through time is critical in understanding how continents are built, disrupted and recycled. While it has become clear that much of the extant Archean crust is underpinned by Archean mantle roots, reports of Proterozoic melt depletion ages for peridotites erupted through Phanerozoic terranes raise the possibility that ancient buoyant lithospheric mantle acts as a "life-raft" for much of the Earth's continental crust. Here we report the largest crust-lithospheric mantle age decoupling (∼2.4 Ga) so far observed on Earth and examine the potential cause for such extreme age decoupling. The Phanerozoic (<300 Ma) continental crust of West Otago, New Zealand, is intruded by Cenozoic diatremes that have erupted cratonic mantle-like highly depleted harzburgites and dunites. These peridotites have rhenium depletion Os model ages that vary from 0.5 to 2.7 Ga, firmly establishing the record of an Archean depletion event. However, the vast range in depletion ages does not correlate with melt depletion or metasomatic tracer indices, providing little support for the presence of a significant volume of ancient mantle root beneath this region. Instead, the chemical and isotopic data are best explained by mixing of relict components of Archean depleted peridotitic mantle residues that have cycled through the asthenosphere over Ga timescales along with more fertile convecting mantle. Extensive melt depletion associated with the "docking" of these melt residues beneath the young continental crust of the Zealandia continent explains the decoupled age relationship that we observe today. Hence, the newly formed lithospheric root incorporates a mixture of ancient and modern mantle derived from the convecting mantle, cooled and accreted in recent times. We argue that in this case, the ancient components played no earlier role in continent stabilization, but their highly depleted nature along with that of their younger counterparts now represents a highly viscous, stable continental keel. This model could account for the large spectrum of ages observed in fertile to moderately depleted peridotites sampled from lithospheric mantle beneath SE Australia, W Antarctica and other locations in Zealandia, as well as the oceanic mantle. Our data confirm the longevity and dispersal of ancient depleted mantle domains in the convecting mantle and their re-appearance beneath young continents.

Constraints on upper mantle Vp/Vs ratio variations beneath eastern North China from receiver function tomography

NASA Astrophysics Data System (ADS)

Si, Shaokun; Tian, Xiaobo; Gao, Rui

2017-05-01

To detect the thinning, modification, and replacement of the basement of the lithosphere is a key step in understanding the destruction mechanism of the North China lithosphere. The difference of the basement of the lithosphere is mainly displayed by the variation of the peridotite composition and its physical state. Vp/Vs ratio (hereafter referred to as velocity ratio) is more sensitive to this change than Vp or Vs alone. By means of the strong dependence of the travel-time of the wave converted at the 410-km discontinuity (P410s) observed in the receiver function (RF) on the velocity ratio in the upper mantle, we developed a new mapping method to constrain the velocity ratio between the Moho and 410-km discontinuity. Using the RFs extracted from 246 broadband stations beneath the North China Craton (NCC), we obtained a high-resolution velocity ratio image of the upper mantle. The abnormal velocity ratio indicates a strong lateral variation of the mineral composition in the upper mantle beneath North China. Two low-velocity-ratio patches are imaged at the top of the upper mantle and the 410 km depth, respectively. The former may be related to the orthopyroxene enrichment in the lithospheric mantle, and the latter may reflect the stagnant Pacific slab in the mantle transition zone (MTZ). A prominent high-velocity-ratio anomaly is also imaged in the upper mantle beneath the Shaanxi-Shanxi rift system in the central NCC, with the highest anomaly reaching 10%. We speculate that the high velocity ratio of upper mantle is related to convective flow due to slab dehydration in the MTZ. The dehydration of the retained slab in the MTZ results in partial melting and upwelling of upper mantle materials. Such convective flow and their melting are closely related to the Cenozoic basalt eruption in the northern section of the Shaanxi-Shanxi rift system.

Sublatitudinal Isotope Heterogeneity of The Atlantic and Adjacent Continents: A Relation To The Litospheric Plates and Superplums

NASA Astrophysics Data System (ADS)

Mironov, Yu. V.; Ryakhovsky, V. M.; Pustovoy, A. A.; Lapidus, I. V.

Four Sr-Nd-Pb isotope sublatitudinal provinces are chosen in the Atlantic and on ad- jacent continents. They include mid-ocean ridges, oceanic rises and islands, as well as Late Mesozoic - Cenozoic continental rifts and traps. A modified Zindler-Hart "man- tle tetrahedron" (1986) have been used for rock systematics. Its major classification element alongside with known end-members (DM, HIMU, EM1, EM2) is any in- tratetrahedron component F ("focal") (Mironov et al., 2000; Rundquist et al., 2000; Ryakhovsky, 2000). It represents average characteristic of all known intratetrahedron components (FOZO, C, PREMA etc.), updated by methods of multidimensional statis- tics. Northern province includes Mid-Atlantic Ridge from a southern part of Reykjanes ridge up to 24S, numerous islands and rises, located at the same latitudes, Cameroon Line, African and European rifts, Aden and Red sea spreading centres, and also Co- mores in Indian ocean. The main composition dispersion of volcanics from withinplate oceanic and continental structures is determined by mixture of F and HIMU (rarely with admixture EM2). MORB within this area are characterized by stable admixture HIMU. Similar composition have the rocks in Bouvet-Antarctic province, within the limits of which the rises Spiss and Shona, the most southern part of Mid-Atlantic ridge, island Bouvet, an adjacent part of Southwest-Indian Ridge, and also traps and rifts on northern coast of Antarctic Continent are located. The Southern province lies in outlines of known Southern hemisphere DUPAL-anomaly (Hart, 1984). The with- inplate oceanic rocks (Gough, Tristan-da-Kunha, Walvis ridge, Rio Grande Plateau, Discovery) correspond to a mixture F + EM1 (sometimes F + EM1 + EM2) and are similar with traps of Southern America and Africa. Further to east this province is traced on islands and mid-ocean ridges in Indian ocean. MORB of Southern Atlantic and Indian ocean are enriched EM1. The Arctic province includes spreading ridges of Northern Atlantic, Norvegian-Greenland sea and Arctic ocean, islands Iceland and Jan-Mayen, Iceland-Faeroe Rise, and also traps of Norway, Britain, and Greenland. MORB and the island rocks correspond to the line of mixture F + DM. On major- ity of isotope characteristics they are similar with DUPAL-MORB (with admixture EM1), but on a ratio 206Pb and 207Pb are close to normal MORB (with admixture 1 HIMU). This specificity is connected to admixture of the special component ARC- TIC. This component represents one of end-components of trends, which are formed by compositions of continental rocks of the Arctic area and reach far beyond "mantle tetrahedron". Thus, transoceanic sublatitudinal isotope heterogeneity, which we have revealed earlier using data on oceanic structures (Mironov et al., 2000; Rundquist et al., 2000; Ryakhovsky, 2000), is traced and on continents. The specificity of main elements of this heterogeneity determine or end-members of "mantle tetrahedron" (HIMU or EM1), or component ARCTIC, located outside "tetrahedron". The main differences between types of structures are determined by mixture of specific compo- nent for given province (HIMU, EM1 or ARCTIC) or with intratetrahedron compo- nent F, or with depleted mantle (DM). The isotopic provinces are discordant to the lithospheric plate boundaries, to extended transform fault, and also to areas of low velosity mantle at the core boundary, which are considered as a places of superplume generating (Fukao et al., 1994). The work is supported by RFBR, and federal program "World Ocean". 2

Progressive enrichment of arc magmas caused by the subduction of seamounts under Nishinoshima volcano, Izu-Bonin Arc, Japan

NASA Astrophysics Data System (ADS)

Sano, Takashi; Shirao, Motomaro; Tani, Kenichiro; Tsutsumi, Yukiyasu; Kiyokawa, Shoichi; Fujii, Toshitsugu

2016-06-01

The chemical composition of intraplate seamounts is distinct from normal seafloor material, meaning that the subduction of seamounts at a convergent margin can cause a change in the chemistry of the mantle wedge and associated arc magmas. Nishinoshima, a volcanic island in the Izu-Bonin Arc of Japan, has been erupting continuously over the past 2 years, providing an ideal opportunity to examine the effect of seamount subduction on the chemistry of arc magmas. Our research is based on the whole-rock geochemistry and the chemistry of minerals within lavas and air-fall scoria from Nishinoshima that were erupted before 1702, in 1973-1974, and in 2014. The mineral phases within the analyzed samples crystallized under hydrous conditions (H2O = 3-4 wt.%) at temperatures of 970 °C-990 °C in a shallow (3-6 km depth) magma chamber. Trace element data indicate that the recently erupted Nishinoshima volcanics are much less depleted in the high field strength elements (Nb, Ta, Zr, Hf) than other volcanics within the Izu-Bonin Arc. In addition, the level of enrichment in the Nishinoshima magmas has increased in recent years, probably due to the addition of material from HIMU-enriched (i.e., high Nb/Zr and Ta/Hf) seamounts on the Pacific Plate, which is being subducted westwards beneath the Philippine Sea Plate. This suggests that the chemistry of scoria from Nishinoshima volcano records the progressive addition of components derived from subducted seamounts.

Reduced lattice thermal conductivity of Fe-bearing bridgmanite in Earth's deep mantle: Reduced Conductivity of Fe-Bridgmanite

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hsieh, Wen-Pin; Deschamps, Frédéric; Okuchi, Takuo

Complex seismic, thermal, and chemical features have been reported in Earth's lowermost mantle. In particular, possible iron enrichments in the large low shear-wave velocity provinces (LLSVPs) could influence thermal transport properties of the constituting minerals in this region, altering the lower mantle dynamics and heat flux across core-mantle boundary (CMB). Thermal conductivity of bridgmanite is expected to partially control the thermal evolution and dynamics of Earth's lower mantle. Importantly, the pressure-induced lattice distortion and iron spin and valence states in bridgmanite could affect its lattice thermal conductivity, but these effects remain largely unknown. Here we precisely measured the lattice thermalmore » conductivity of Fe-bearing bridgmanite to 120 GPa using optical pump-probe spectroscopy. The conductivity of Fe-bearing bridgmanite increases monotonically with pressure but drops significantly around 45 GPa due to pressure-induced lattice distortion on iron sites. Our findings indicate that lattice thermal conductivity at lowermost mantle conditions is twice smaller than previously thought. The decrease in the thermal conductivity of bridgmanite in mid-lower mantle and below would promote mantle flow against a potential viscosity barrier, facilitating slabs crossing over the 1000 km depth. Modeling of our results applied to LLSVPs shows that variations in iron and bridgmanite fractions induce a significant thermal conductivity decrease, which would enhance internal convective flow. Our CMB heat flux modeling indicates that while heat flux variations are dominated by thermal effects, variations in thermal conductivity also play a significant role. The CMB heat flux map we obtained is substantially different from those assumed so far, which may influence our understanding of the geodynamo.« less

Reduced Lattice Thermal Conductivity of Fe-bearing Bridgmanite in Earth's Deep Mantle

NASA Astrophysics Data System (ADS)

Hsieh, W. P.; Deschamps, F.; Okuchi, T.; Lin, J. F.

2017-12-01

Complex seismic and thermo-chemical features have been revealed in Earth's lowermost mantle. Particularly, possible iron enrichments in the large low shear-wave velocity provinces (LLSVPs) could influence thermal transport properties of the constituting minerals in this region, which, in turn, may alter the lower mantle dynamics and heat flux across core-mantle boundary (CMB). Thermal conductivity of bridgmanite is expected to partially control the thermal evolution and dynamics of Earth's lower mantle. Importantly, the pressure-induced lattice distortion in bridgmanite could affect its lattice thermal conductivity, but this effect remains largely unknown. Here we report our measurements of the lattice thermal conductivity of Fe-bearing and (Fe,Al)-bearing bridgmanites to 120 GPa using optical pump-probe spectroscopy. The thermal conductivity of Fe-bearing bridgmanite increases monotonically with pressure, but drops significantly around 45 GPa presumably due to pressure-induced lattice distortion on iron sites. Our findings indicate that lattice thermal conductivity at lowermost mantle conditions is twice smaller than previously thought. The decrease in the thermal conductivity of bridgmanite in mid-lower mantle and below would promote mantle flow against a potential viscosity barrier, facilitating slabs crossing over the 1000-km depth. Modeling of our results applied to the LLSVPs shows that variations in iron and bridgmanite fractions induce a significant thermal conductivity decrease, which would enhance internal convective flow. Our CMB heat flux modeling indicates that, while heat flux variations are dominated by thermal effects, variations in thermal conductivity also play a significant role. The CMB heat flux map we obtained is substantially different from those assumed so far, which may influence our understanding of the geodynamo.

Comparing the composition of the earliest basalts erupted by the Iceland and Afar mantle plumes.

NASA Astrophysics Data System (ADS)

Stuart, Finlay M.

2013-04-01

The first basalts erupted by mantle plumes are typically generated by mantle melting at temperatures 200-300°C higher than average ambient mantle. This is consistent with the derivation of from a thermal boundary layer at the core-mantle boundary. Mantle plume temperatures decrease with time, likely as large plume heads give way to thin plume conduits. Consequently the early, hot plume basalts are a window into the deep mantle. At it's simplest they provide a test of whether the discrete plume source regions are primordial mantle that have been isolated since soon after Earth accretion, or have substantial contributions from subducted slabs. Here I present new isotopic and trace element determinations of the earliest picritic basalts from the ~30 Ma Afar plume in Ethiopia. They will be compared with similar material from the ~60 Ma proto-Iceland plume (PIP) in an effort to test prevailing models regarding the source of mantle plumes. The extremely primordial nature of the helium in the PIP picrites (3He/4He ~ 50 Ra) contrasts with much lower values of the Ethiopian flood basalt province (~21 Ra). The Iceland plume 3He/4He has decreased (linearly) with time, mirroring the secular cooling of the Iceland mantle plume identified by decreasing MgO and FeO in primary melts. In 60 million years the Iceland plume 3He/4He is still higher than the maximum Afar plume value. The Sr-Nd-Pb isotopic composition of the high 3He/4He Ethiopian flood basalt province picrites are remarkably homogenous (e.g. 87Sr/86Sr = 0.70396-0.70412; 206Pb/204Pb = 18.82-19.01). In comparison the PIP picrites have ranges that span nearly the global range of E-MORB and N-MORB. The Afar and proto-Iceland mantle plumes are clearly not initiated in a single deep mantle domain with the same depletion/enrichment and degassing histories, and the same scale of heterogeneity. This implies that there is more than one plume source region/mechanism that is capable of generating comparable volumes of basalt melt at Earth surface.

Xenon isotopic composition of the Mid Ocean Ridge Basalt (MORB) source

NASA Astrophysics Data System (ADS)

Peto, M. K.; Mukhopadhyay, S.

2012-12-01

Although convection models do not preclude preservation of smaller mantle regions with more pristine composition throughout Earth's history, it has been widely assumed that the moon forming giant impact likely homogenizes the whole mantle following a magma ocean that extended all the way to the bottom of the mantle. Recent findings of tungsten and xenon heterogeneities in the mantle [1,2,3,4], however, imply that i) the moon forming giant impact may not have homogenized the whole mantle and ii) plate tectonics was inefficient in erasing early formed compositional differences, particularly for the xenon isotopes. Therefore, the xenon isotope composition in the present day mantle still preserves a memory of early Earth processes. However, determination of the xenon isotopic composition of the mantle source is still scarce, since the mantle composition is overprinted by post-eruptive atmospheric contamination in basalts erupted at ocean islands and mid ocean ridges. The xenon composition of the depleted upper mantle has been defined by the gas rich sample, 2πD43 (also known as "popping rock"), from the North Atlantic (13° 469`N). However, the composition of a single sample is not likely to define the composition of the upper mantle, especially since popping rock has an "enriched" trace element composition. We will present Ne, Ar and Xe isotope data on MORB glass samples with "normal" helium isotope composition (8±1 Ra) from the Southeast Indian Ridge, the South Atlantic Ridge, the Sojourn Ridge, the Juan de Fuca, the East Pacific Rise, and the Gakkel Ridge. Following the approach of [1], we correct for syn- and post-eruptive atmosphere contamination, and determine the variation of Ar and Xe isotope composition of the "normal" MORB source. We investigate the effect of atmospheric recycling in the variation of MORB mantle 40Ar/36Ar and 129Xe/130Xe ratios, and attempt to constrain the average upper mantle argon and xenon isotopic compositions. [1] Mukhopadhyay, Nature 2012; [2] Tucker et al., EPSL (in review); [3] Moreira et al., Nature 1998 [4] Touboul et al., Science 2012.

Archean recycled oceanic crust sampled in Azores lavas

NASA Astrophysics Data System (ADS)

Beguelin, P.; Bizimis, M.; Beier, C.; Turner, S.

2016-12-01

Azores lava compositions extend below the mantle array in ɛNd-ɛHf space and define the steepest slope of all plume provinces [1], but this pattern is largely controlled by low ɛHf lavas from Eastern São Miguel island (SM). Here we present new Hf isotope data on well-characterized on-land and submarine Azores lavas from several islands, the Terceira Rift and João do Castro seamount (JdC), in order to further constrain this trend. While Azores lavas fall along the mantle array with relatively steep slopes (e.g. São Jorge slope = 2.1), both SM and JdC fall below the mantle array as two distinct steep arrays with slopes of 2.0 and 2.6 respectively, extending to ɛHf = 0 at ɛNd = 2 (SM) and 4 (JdC). This is a unique feature in OIBs. The new Hf-Nd data overlaps the HIMU-type Mangaia and St Helena compositions. However, SM and JdC have distinctly less radiogenic and more variable Pb isotopes (e.g. 206Pb/204Pb = 18.8 to 20.2) than HIMU. Hf-Nd isotope decoupling below the mantle array is therefore not an exclusive HIMU signature. The coupled Hf-Nd-Pb-Sr isotope compositions of the enriched SM and JdC end-members can be modeled by recycled 2.5-3.0 Ga N-MORB, with some E-MORB affinity for SM. Unlike HIMU however, no Pb-loss during subduction is required for recycled MORB to explain their Pb isotopes. The relatively high κ (232Th/238U 4.3) required by the Azores data is also consistent with a high Th/U Archean mantle [2]. Aged, metasomatised mantle lithosphere based on a global peridotite and pyroxenite compilation is too variable and only fortuitously could explain the Azores compositions. Both enriched JdC and SM endmembers can therefore be explained by a recycled Archean oceanic crust that is locally heterogeneous, as presently observed in some MOR segments where N-and E-MORB exist closely [3, 4]. The lack of mixing between SM and JdC end-members some 100 km apart further implies that this recycled crust has retained its distinct signature through mantle convection and stirring for 2.5-3.0 Ga. [1] Salters et al. (2011) G3 12(8): Q08001. [2] Elliott et al. (1999) EPSL 169(1), 129-145. [3] Donnelly et al. (2004) EPSL 226(3), 347-366. [4] Gale et al. (2013) EPSL 365, 209-220.

Predicting Global Rates and Distribution of Carbonate Melting Beneath the Ocean Basins: Implications for the Origin of the Gutenberg Discontinuity

NASA Astrophysics Data System (ADS)

Clerc, F.; Behn, M. D.; Parmentier, E. M.

2017-12-01

The pooling of carbonate melts beneath old ocean lithosphere is a proposed explanation for the seismic Gutenberg (G) discontinuity. However, while the G discontinuity is observed ubiquitously across the ocean basins, carbonate melting only occurs in regions of mantle upwelling. Here we examine the global distribution and extent of carbonate melting by coupling a mantle flow model with a thermodynamic parameterization for carbonate melting. We obtain global upwelling velocities from a convection model driven by plate motions and mantle density differences [1], and calculate melt fractions from the R_DMC carbonate solidus [2]. We find low-degree carbonate melts are produced pervasively throughout ocean basins, driven by passive upwelling in response to subduction. Assuming melt formed within 100 km of the ridge is focused to its axis, our model predicts a 6-km thick oceanic crust and a global CO2 ridge flux of 7 x 1011 mol/yr (for a mantle source concentration of 100 ppm CO2). This flux is consistent with other estimates of CO2 ridge fluxes [e.g.,3] over the inferred range of MORB-source mantle carbon concentrations [e.g.,4]. In addition to the ridge flux, off-axis carbonate melting results in a global CO2 flux of 1.6 x 1012mol/yr. To test for correlations between regions of upwelling-induced carbonate melting and seismic evidence for the LAB, we compare our results with a compilation of seismic G discontinuity observations [5]. While most observations of the G discontinuity are found in regions of predicted carbonate melting, some lie in regions of downwelling (where no melting occurs), suggesting that melt pooling does not conclusively explain these seismic signals. Further, we estimate off-axis porosities to be < 0.1%, indicating that the melt remaining in the mantle does not contribute substantially to a discontinuity of the observed magnitude. Carbonate melts pooled at the base of the lithosphere may refreeze within the thermal boundary layer and refertilize the lithosphere. We model the trace element compositions of these enriched melts and compare them with geochemical data from enriched mantle sources, such as petit-spot melts [e.g.,6]. [1] Naliboff et al., GRL, 2009; [2] Keller & Katz, J Pet, 2016; [3] Chavrit et al., EPSL, 2014; [4] Rosenthal et al., EPSL, 2015; [5] Schmerr, Sci, 2012; [6] Machida et al., EPSL, 2015

The mantle and crustal evolution of two garnet peridotite suites from the Western Gneiss Region, Norwegian Caledonides: An isotopic investigation

NASA Astrophysics Data System (ADS)

Brueckner, H. K.; Carswell, D. A.; Griffin, W. L.; Medaris, L. G., Jr.; Van Roermund, H. L. M.; Cuthbert, S. J.

2010-06-01

A compilation of published and unpublished geochronological and isotopic data from garnet-bearing orogenic peridotites in the HP/UHP Western Gneiss Region (WGR) of the Norwegian Caledonides indicate a common origin for all WGR peridotites, followed by different, though related, Proterozoic and Phanerozoic histories for those in the northwestern WGR (NW peridotites) compared to those in the central and western WGR (CW peridotites). All peridotites are refractory fragments of the subcontinental lithosphere generated by Archean melt extraction, which produced strongly depleted dunites and harzburgites with relict orthopyroxene and majoritic garnet megacrysts (M 1NW) within the NW peridotites. The Archean history is preserved by Re-Os sulfide and whole-rock ages from several WGR bodies and by Sm-Nd ages from the M 1NW megacrysts. Subsequently the CW peridotites were re-fertilized within the lithospheric mantle by mid-Proterozoic or older silicate melts that generated M 2CW garnet pyroxenites and adjacent garnet peridotites. Clinopyroxenes from these bodies show large variation in 143Nd/ 144Nd, but nearly constant 87Sr/ 86Sr, suggesting autometasomatism of depleted mantle by LREE-enriched, Rb-poor melts derived from equally depleted mantle. NW peridotites lack mid-Proterozoic garnet pyroxenite intrusions, but M 2NW garnet-rich assemblages that exsolved from relict M 1 megacrysts may have equilibrated at the same time as the M 2CW refertilization. Sm-Nd and Lu-Hf mineral apparent isochron ages from both suites range from 1.75 to ca. 0.87 Ga. The age spectrum suggests continuous diffusion among M 2 minerals that formed ≥ 1.75 Ga ago punctuated by partial re-equilibration during a 1.0 Ga thermal event. Much later the NW peridotites were transferred from the mantle wedge into the crust as the WGR was subducted into the mantle during the ca 400 Ma Scandian Orogeny. Further subduction heterogeneously metasomatized and recrystallized the NW peridotites to form M 3NW garnet, clinopyroxene and, where metasomatism was pervasive, new M 3NW radiogenic ( 87Sr/ 86Sr > 0.715), LIL-enriched minerals (phlogopite, amphibole) and microdiamond consistent with invasion by hydrous fluids from the enclosing Proterozoic gneisses. Nine young apparent ages (672 to 424 Ma), all from exsolved or recrystallized garnets within NW peridotites, represent mixed (M 2NW and M 3NW) apparent ages. The three youngest ages (weighted mean of 429.5 ± 3.1 Ma; 2 σ) may date M 3NW prograde re-equilibration during earliest Scandian subduction. The CW peridotites show no evidence of prograde M 3 re-equilibration, suggesting derivation from a different part of the Laurentian mantle wedge during the exhumation of the WGR from the mantle.

Lithospheric mantle evolution above a subducting plate: Direct constraints from Antarctic Peninsula spinel peridotite xenoliths

NASA Astrophysics Data System (ADS)

Gibson, Lydia; Gibson, Sally; Leat, Phil

2010-05-01

Our understanding of the tectono-magmatic processes in subduction zones generally relies on interpretations of the bulk-rock compositions of associated volcanic rocks. These, however, have typically undergone extensive modification in the crust (fractionation and/or contamination) and interpreting the mantle processes that have contributed to their genesis is complex. Direct evidence of the composition of the mantle beneath subduction-related volcanics is rare as mantle xenoliths are seldom brought to the surface. An exception is the Antarctic Peninsula, which consists of a series of suspect arc terranes accreted to the margin of Gondwana. Subduction occurred along a trench, off the west coast, and lasted over 200 Ma. It finally ceased after a series of ridge-trench collisions, which began at ~50 Ma in the south and ended at ca. 4 Ma in the north. This was followed by extensive alkaline volcanism along the length of the Antarctic Peninsula. At several localities these post-subduction volcanics contain abundant, fresh spinel-bearing lherzolites, harzburgites and pyroxenites. The widest variety of xenoliths were collected from basanites and tephrites emplaced on Alexander Island and Rothschild Island in the accreted Western Domain. The mineral chemistry of the xenolith suite as a whole is highly varied, e.g. olivine ranges in composition from Fo77 to Fo91, but within individual xenoliths typically only limited variation is apparent. Xenolith textures and plots of mineral chemistry suggest that the constituent mineral phases are in equilibrium and can be used to determine pressures and temperatures. PT estimates based on pyroxene compositions indicate that the lithosphere beneath the Antarctic Peninsula has a normal, unperturbed mantle geotherm and a thickness of ~90 km; the base of the mechanical boundary layer is at ~70 km and the xenoliths appear to have been entrained from within this region. Preliminary modelling of incompatible-trace-element ratios of diopsides and augites in the peridotites suggests that they are not all simple residues of mantle melting. They have a wide range of [La/Sm]n ratios (0.01 to 8.56) and appear to have undergone variable degrees of modal metasomatism, which has also resulted in an increase in bulk-rock concentrations of major elements, such as Fe and Al. Variable Ti enrichment in spinels and very-high oxygen fugacities suggest that an extreme range of melt compositions may have interacted with the mantle beneath the Antarctic Peninsula and produced the diverse lithologies that we have observed in the mantle xenolith suite. These include boninites (Mg-rich, hydrous melts) and small-fraction melts. We propose that metasomatic enrichment by silicate melts may have occurred during subduction whereas carbonate metasomatism modified the lithosphere following the formation of a 'window' in the underlying slab.

Non-chondritic iron isotope ratios in planetary mantles as a result of core formation

NASA Astrophysics Data System (ADS)

Elardo, Stephen M.; Shahar, Anat

2017-02-01

Information about the materials and conditions involved in planetary formation and differentiation in the early Solar System is recorded in iron isotope ratios. Samples from Earth, the Moon, Mars and the asteroid Vesta reveal significant variations in iron isotope ratios, but the sources of these variations remain uncertain. Here we present experiments that demonstrate that under the conditions of planetary core formation expected for the Moon, Mars and Vesta, iron isotopes fractionate between metal and silicate due to the presence of nickel, and enrich the bodies' mantles in isotopically light iron. However, the effect of nickel diminishes at higher temperatures: under conditions expected for Earth's core formation, we infer little fractionation of iron isotopes. From our experimental results and existing conceptual models of magma ocean crystallization and mantle partial melting, we find that nickel-induced fractionation can explain iron isotope variability found in planetary samples without invoking nebular or accretionary processes. We suggest that near-chondritic iron isotope ratios of basalts from Mars and Vesta, as well as the most primitive lunar basalts, were achieved by melting of isotopically light mantles, whereas the heavy iron isotope ratios of terrestrial ocean floor basalts are the result of melting of near-chondritic Earth mantle.

Electrical structure of the lithosphere across the Western Paraná suture zone: the role of a Neoproterozoic-Cambrian subduction in generating the Paraná Magmatic Province

NASA Astrophysics Data System (ADS)

Dragone, G. N.; Bologna, M.; Gimenez, M. E.; Alvarez, O.; Lince Klinger, F. G.; Correa-Otto, S.; Ussami, N.

2017-12-01

The Paraná Magmatic Province (PMP) together with the Etendeka Province (EP) in Africa is one of the Earth's largest igneous provinces originated prior to the Western Gondwanaland break-up and the inception of the South Atlantic Ocean in the Lower Cretaceous. Geochemical data of PMP-EP basalts collected since late 1980's indicate the origin of PMP-EP by melting of a heterogeneous and enriched subcontinental lithospheric mantle with fast rate of eruption (< 3 My). The geodynamical cause of this magmatism is still a matter of debate (deep mantle plume x plate model). New isotopic geochemical data from Re-Os systematics (Rocha-Jr et al., 2012, EPSL) of PMP basalts indicate metasomatized asthenospheric mantle component probably generated at the mantle wedge between the PMP-EP lithosphere and the subducting oceanic plate. A combined seismic velocity and density model of PMP by Chaves et al. (2016, G3) indicates high velocity and a density increase of PMP ancient lithosphere interpreted as due to a long-term mantle refertilization process. To investigate the role of the subduction zones in the development of both the Paraná basin subsidence and the magmatic province we present the results of regional scale broad-band MT-magnetotelluric soundings across the western and southern borders of the PMP, the Western Paraná suture zone (WPS in Fig. 1). We discuss the electrical properties of the lithosphere along three MT profiles across the WPS. MT-A profile (Padilha et al., 2015, JGR) extends from Rio Apa craton towards the center of PMP (high-TiO2 basalts). Profile MT-B extends from Tebicuary craton towards the center of PMP (low-TiO2) and profile MT-C extends from Rio de la Plata craton towards the southern PMP (low- and high-TiO2). All profiles show a resistive ( 104 ohm m) and thick (> 150 km) lithosphere in the cratonic areas whereas the electrical lithosphere is thinner (<100 km) with alternating high and low resistivities within PMP. Vertically elongated and high electrical conductivity anomalies ( 10 ohm m) centered at 40 km depth occur along the -30 mGal contour line in the three profiles, and are interpreted as the location of the suture and former subduction zone. We will discuss the correlation between geochemical and petrological characteristics of basalts and the electrical properties of the lithospheric mantle underneath.

Inclusions in diamonds constrain thermo-chemical conditions during Mesozoic metasomatism of the Kaapvaal cratonic mantle

NASA Astrophysics Data System (ADS)

Weiss, Yaakov; Navon, Oded; Goldstein, Steven L.; Harris, Jeff W.

2018-06-01

Fluid/melt inclusions in diamonds, which were encapsulated during a metasomatic event and over a short period of time, are isolated from their surrounding mantle, offering the opportunity to constrain changes in the sub-continental lithospheric mantle (SCLM) that occurred during individual thermo-chemical events, as well as the composition of the fluids involved and their sources. We have analyzed a suite of 8 microinclusion-bearing diamonds from the Group I De Beers Pool kimberlites, South Africa, using FTIR, EPMA and LA-ICP-MS. Seven of the diamonds trapped incompatible-element-enriched saline high density fluids (HDFs), carry peridotitic mineral microinclusions, and substitutional nitrogen almost exclusively in A-centers. This low-aggregation state of nitrogen indicates a short mantle residence times and/or low mantle ambient temperature for these diamonds. A short residence time is favored because, elevated thermal conditions prevailed in the South African lithosphere during and following the Karoo flood basalt volcanism at ∼180 Ma, thus the saline metasomatism must have occurred close to the time of kimberlite eruptions at ∼85 Ma. Another diamond encapsulated incompatible-element-enriched silicic HDFs and has 25% of its nitrogen content residing in B-centers, implying formation during an earlier and different metasomatic event that likely relates to the Karoo magmatism at ca. 180 Ma. Thermometry of mineral microinclusions in the diamonds carrying saline HDFs, based on Mg-Fe exchange between garnet-orthopyroxene (Opx)/clinopyroxene (Cpx)/olivine and the Opx-Cpx thermometer, yield temperatures between 875-1080 °C at 5 GPa. These temperatures overlap with conditions recorded by touching inclusion pairs in diamonds from the De Beers Pool kimberlites, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250 °C compared to P-T gradients recorded by peridotite xenoliths from the same locality. Oxygen fugacity (fO2) differs as well. The fO2 calculated for the saline HDF compositions (Δlog ⁡ fO 2 (FMQ) = - 2.47 to -1.34) are higher by about a log unit compared with that recorded by xenoliths at 4-7 GPa. We conclude that enriched saline HDFs mediated the metasomatism that preceded Group I kimberlite eruptions in the southwestern Kaapvaal craton, and that their 'cold and oxidized' nature reflects their derivation from a deep subducting slab. This event had little impact on the temperature and redox state of the Kaapvaal lithosphere as a reservoir, however, it likely affected its properties along limited metasomatized veins and their wall rock. To reconcile the temperature and oxygen fugacity discrepancy between inclusions in diamonds and xenoliths, we argue that xenoliths did not equilibrate during the last saline metasomatic event or kimberlite eruption. Thus the P-T- fO2 gradients they record express pre-existing lithospheric conditions that were likely established during the last major thermal event in the Kaapvaal craton (i.e. the Karoo magmatism at ca. 180 Ma).

Evidence for a Heterogeneous Distribution of Water in the Martian Interior

NASA Technical Reports Server (NTRS)

McCubbin, Francis; Boyce, Jeremy W.; Srinvasan, Poorna; Santos, Alison R.; Elardo, Stephen M.; Filiberto, Justin; Steele, Andrew; Shearer, Charles K.

2016-01-01

The abundance and distribution of H2O within the terrestrial planets, as well as its timing of delivery, is a topic of vital importance for understanding the chemical and physical evolution of planets and their potential for hosting habitable environments. Analysis of planetary materials from Mars, the Moon, and the eucrite parent body (i.e., asteroid 4Vesta) have confirmed the presence of H2O within their interiors. Moreover, H and N isotopic data from these planetary materials suggests H2O was delivered to the inner solar system very early from a common source, similar in composition to the carbonaceous chondrites. Despite the ubiquity of H2O in the inner Solar System, the only destination with any prospects for past or present habitable environments at this time, outside of the Earth, is Mars. Although the presence of H2O within the martian interior has been confirmed, very little is known regarding its abundance and distribution within the martian interior and how the martian water inventory has changed over time. By combining new analyses of martian apatites within a large number of martian meteorite types with previously published volatile data and recently determined mineral-melt partition coefficients for apatite, we report new insights into the abundance and distribution of volatiles in the martian crust and mantle. Using the subset of samples that did not exhibit crustal contamination, we determined that the enriched shergottite mantle source has 36-73 ppm H2O and the depleted shergottite mantle source has 14-23 ppm H2O. This result is consistent with other observed geochemical differences between enriched and depleted shergottites and supports the idea that there are at least two geochemically distinct reservoirs in the martian mantle. We also estimated the H2O content of the martian crust using the revised mantle H2O abundances and known crust-mantle distributions of incompatible lithophile elements. We determined that the bulk martian crust has approximately 1400 ppm H2O, which is likely distributed toward the martian surface. This crustal water abundance would equate to a global equivalent layer (GEL) of water at a depth of-229 m, which can account for at least some of the surface features on Mars attributed to flowing water and may be sufficient to support the past presence of a shallow sea on Mars' surface.

A SoxC gene related to larval shell development and co-expression analysis of different shell formation genes in early larvae of oyster.

PubMed

Liu, Gang; Huan, Pin; Liu, Baozhong

2017-06-01

Among the potential larval shell formation genes in mollusks, most are expressed in cells surrounding the shell field during the early phase of shell formation. The only exception (cgi-tyr1) is expressed in the whole larval mantle and thus represents a novel type of expression pattern. This study reports another gene with such an expression pattern. The gene encoded a SoxC homolog of the Pacific oyster Crassostrea gigas and was named cgi-soxc. Whole-mount in situ hybridization revealed that the gene was highly expressed in the whole larval mantle of early larvae. Based on its spatiotemporal expression, cgi-soxc is hypothesized to be involved in periostracum biogenesis, biomineralization, and regulation of cell proliferation. Furthermore, we investigated the interrelationship between cgi-soxc expression and two additional potential shell formation genes, cgi-tyr1 and cgi-gata2/3. The results confirmed co-expression of the three genes in the larval mantle of early D-veliger. Nevertheless, cgi-gata2/3 was only expressed in the mantle edge, and the other two genes were expressed in all mantle cells. Based on the spatial expression patterns of the three genes, two cell groups were identified from the larval mantle (tyr1 + /soxc + /gata2/3 + cells and tyr1 + /soxc + /gata2/3 - cells) and are important to study the differentiation and function of this tissue. The results of this study enrich our knowledge on the structure and function of larval mantle and provide important information to understand the molecular mechanisms of larval shell formation.

Microstructures, composition, and seismic properties of the Ontong Java Plateau mantle root

NASA Astrophysics Data System (ADS)

Tommasi, Andréa.; Ishikawa, Akira

2014-11-01

To study how an impacting plume modifies the mantle lithosphere, we analyzed the microstructures and crystal preferred orientations (CPO) of 29 peridotites and 37 pyroxenites that sample the mantle root of the Ontong Java Plateau (OJP) from 60 to 120 km depth. The peridotites show a strong compositional variability, but homogeneous coarse granular to tabular microstructures, except for those equilibrated at the shallowest and deepest depths, which are porphyroclastic. All peridotites have clear olivine CPO, with dominant fiber-[010] patterns. Low intragranular misorientations and straight grain boundaries in olivine suggest that, above 100 km depth, annealing often followed deformation. Calculated density and P wave velocities of the peridotites decrease weakly with depth. S wave velocities decrease faster, resulting in increasing Vp/Vs ratio with depth. Calculated densities and seismic velocity profiles are consistent with those estimated for normal mantle compositions under a cold oceanic geotherm. Enrichment in pyroxenites may further increase seismic velocities. The calculated seismic properties cannot therefore explain the low S waves velocities predicted by Rayleigh wave tomography and ScS data in the mantle beneath the OJP. Calculated P and S waves anisotropy is variable (2-12%). It is higher on average in the deeper section of the lithosphere. Because olivine has dominantly [010]-fiber CPO patterns, if foliations are horizontal, vertically propagating S waves and Rayleigh waves will sample very weak anisotropy in the OJP mantle lithosphere. Moreover, if the orientation of the lineation changes with depth, the anisotropy-induced contrast in seismic properties might produce an intralithospheric reflector marking the stratification of the OJP mantle root.

A wet, heterogeneous lunar interior: Lower mantle and core dynamo evolution

NASA Astrophysics Data System (ADS)

Evans, A. J.; Zuber, M. T.; Weiss, B. P.; Tikoo, S. M.

2014-05-01

While recent analyses of lunar samples indicate the Moon had a core dynamo from at least 4.2-3.56 Ga, mantle convection models of the Moon yield inadequate heat flux at the core-mantle boundary to sustain thermal core convection for such a long time. Past investigations of lunar dynamos have focused on a generally homogeneous, relatively dry Moon, while an initial compositionally stratified mantle is the expected consequence of a postaccretionary lunar magma ocean. Furthermore, recent re-examination of Apollo samples and geophysical data suggests that the Moon contains at least some regions with high water content. Using a finite element model, we investigate the possible consequences of a heterogeneously wet, compositionally stratified interior for the evolution of the Moon. We find that a postoverturn model of mantle cumulates could result in a core heat flux sufficiently high to sustain a dynamo through 2.5 Ga and a maximum surface, dipolar magnetic field strength of less than 1 μT for a 350-km core and near ˜2 μT for a 450-km core. We find that if water was transported or retained preferentially in the deep interior, it would have played a significant role in transporting heat out of the deep interior and reducing the lower mantle temperature. Thus, water, if enriched in the lower mantle, could have influenced core dynamo timing by over 1.0 Gyr and enhanced the vigor of a lunar core dynamo. Our results demonstrate the plausibility of a convective lunar core dynamo even beyond the period currently indicated by the Apollo samples.

The record of mantle heterogeneity preserved in Earth's oceanic crust

NASA Astrophysics Data System (ADS)

Burton, K. W.; Parkinson, I. J.; Schiano, P.; Gannoun, A.; Laubier, M.

2017-12-01

Earth's oceanic crust is produced by melting of the upper mantle where it upwells beneath mid-ocean ridges, and provides a geographically widespread elemental and isotopic `sample' of Earth's mantle. The chemistry of mid-ocean ridge basalts (MORB), therefore, holds key information on the compositional diversity of the upper mantle, but the problem remains that mixing and reaction during melt ascent acts to homogenise the chemical variations they acquire. Nearly all isotope and elemental data obtained thus far are for measurements of MORB glass, and this represents the final melt to crystallise, evolving in an open system. However, the crystals that are present are often not in equilibrium with their glass host. Melts trapped in these minerals indicate that they crystallised from primitive magmas that possess diverse compositions compared to the glass. Therefore, these melt inclusions preserve information on the true extent of the mantle that sources MORB, but are rarely amenable to precise isotope measurement. An alternative approach is to measure the isotope composition of the primitive minerals themselves. Our new isotope data indicates that these minerals crystallised from melts with significantly different isotope compositions to their glass host, pointing to a mantle source that has experienced extreme melt depletion. These primitive minerals largely crystallised in the lower oceanic crust, and our preliminary data for lower crustal rocks and minerals shows that they preserve a remarkable range of isotope compositions. Taken together, these results indicate that the upper mantle sampled by MORB is extremely heterogeneous, reflecting depletion and enrichment over much of Earth's geological history.