Water in Earth's mantle: Hydrogen analysis of mantle olivine, pyroxenes and garnet using the SIMS

NASA Technical Reports Server (NTRS)

Kurosawa, Masanori; Yurimoto, Hisayoshi; Sueno, Shigeho

1993-01-01

Hydrogen (or water) in the Earth's interior plays a key role in the evolution and dynamics of the planet. However, the abundance and the existence form of the hydrogen have scarcely been clear in practice. Hydrogen in the mantle was incorporated in the interior during the formation of the Earth. The incorporated hydrogen was hardly possible to concentrate locally inside the Earth considering its high mobility and high reactivity. The hydrogen, preferably, could be distributed homogeneously over the mantle and the core by the subsequent physical and chemical processes. Therefore, hydrogen in the mantle could be present in the form of trace hydrogen in nominally anhydrous mantle minerals. The hydrogen and the other trace elements in mantle olivines, orthopyroxenes, clinopyroxenes, and garnets were determined using secondary ion mass spectrometry (SIMS) for elucidating (1) the exact hydrogen contents, (2) the correlation between the hydrogen and the other trace elements, (3) the dependence of the hydrogen contents on the depth, and (4) the dependence of the whole rock water contents on the depth.

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.

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

Trace element mobility at the slab-mantle interface: constraints from "hybrid

NASA Astrophysics Data System (ADS)

Marocchi, M.; Tropper, P.; Mair, V.; Bargossi, G. M.; Hermann, J.

2009-04-01

Subduction mélanges and hybrid rocks are considered, together with mafic rocks, metasediments and serpentinite as an important volatile-bearing portion of subducting slabs (cf. Spandler et al., 2008 and references therein; Miller et al., 2009). In particular, metasomatic rocks occurring in exhumed HP mélanges have recently attracted growing interest for two main reasons: i) metasomatic rocks forming at the interface between ultramafic and crustal rocks of subducting slabs constitute new bulk compositions which can affect the redistribution of major and trace elements and modify the composition of slab fluids moving to the mantle wedge and ii) these mineral assemblages, consisting mainly of hydrous phases can potentially store and transport water at great depth in subduction zones. Ultramafic rocks belonging to the Hochwart peridotite (Ulten Zone, central-eastern Italian Alps) preserve a series of metasomatic mineral zones generated by infiltration of hydrous fluids/melts, which occurred at the gneiss-peridotite interface (Tumiati et al., 2007; Marocchi et al., 2009). The peridotite body of Mt. Hochwart represents an almost unique occurrence where subduction-related mantle metasomatism can be studied on an outcrop scale. The ultramafic body consists of metaperidotites exposed as a hectometre-size lens along a steep gully, associated to monomineralic zones that developed at the contact between the peridotite body and the garnet-bearing gneiss country rocks. The formation of the metasomatic zones composed exclusively of hydrous phases involved extensive H2O-metasomatism as already documented for the Ulten peridotites (Scambelluri et al., 2006; Marocchi et al., 2007). Whole-rock geochemistry and trace element composition of hydrous phases (phlogopite and amphibole) in different metasomatic zones indicate mobility of many elements, including elements such as Ta, which are considered to have scarce mobility in fluids. Trace element composition of accessory minerals in the phlogopite-rich zone suggests that the trace element signature of subduction zone fluids may be fractionated in this zone. The progressive depletion in some trace elements (LREE and LILE) and enrichment in Li from the gneiss towards the peridotite suggests a strong influence of bulk composition on the trace element budget of hydrous minerals. Since these metasomatic zones can be representative of the processes occurring at the slab-mantle interface, we can infer that metasomatic reactions between slab-derived fluids and ultramafic mantle wedge will follow a specific series of reactions and create mineral zones similar to those observed in this study. Despite the mobility of many elements, in the trace element profiles for amphibole and phlogopite across the different zones, we observe a rapid decrease even of the "fluid mobile" element contents within the reaction zone. With the exception of Li, we assist to an abrupt decrease of most of trace element concentrations going towards the peridotite side contact. Thus, according to the present study, it is not likely that the "crustal trace element signature" (i.e. LILE and LREE-enriched) could be able to travel far into the mantle. Our results further favour the evidence that the primary composition of subduction zone fluids reaching the source region of arc magmas is substantially modified by metasomatic reactions occurring in the mantle wedge. Furthermore, we underline that metasomatic rocks such as those observed at Mt. Hochwart are potentially able to transport H2O and other trace elements to greater depths in subduction zones. References: Marocchi M, Hermann J, Morten L (2007)-Lithos 99: 85-104. Marocchi M, Mair V, Tropper P, Bargossi GM (2009)-Mineral Petrol, in press Miller DP, Marschall RH, Schumacher JC (2009)- Lithos 107: 53-67. Scambelluri M, Hermann J, Morten L, Rampone E (2006)- Contrib Mineral Petrol 151:372-394. Spandler CJ, Hermann J, Faure K, Mavrogenes JA, Arculus RJ (2008)- Contrib Mineral Petrol 155: 181-198. Tumiati S, Godard G, Martin S, Klőtzli U, Monticelli D (2007)- Lithos 94: 148-167.

Petrogenesis of High-CaO Lavas Recovered from Hawaii Scientific Drilling Project

NASA Astrophysics Data System (ADS)

Huang, S.

2015-12-01

Mauna Kea tholeiitic lavas recovered from Hawaii Scientific Drilling Project (HSDP) can be divided into three groups based on their major element compositions: High-SiO2, Low-SiO2, and High-CaO groups. Detailed geochemical and isotopic studies have been focused on the High- and Low-SiO2 group lavas, and High-CaO lavas were not well studied because they were not included in the original reference suite samples. Here we report trace element compositions determined on a suite of High-CaO glasses, and use these data to constrain the petrogenesis of High-CaO lavas. When normalized to Low-SiO2 lavas, High-CaO lavas form a U-shaped trace element pattern. That is, High-CaO lavas are enriched in both the most (Nb, Th) and the least (Sc, V) incompatible elements. This trace element difference is best explained if High-CaO parental magma represents a mixture of low degree partial melt of the Low-SiO2 mantle source and a mafic cumulate component. This mafic cumulate must be clinopyroxene-rich, and it could be delaminated mafic cumulate formed under arcs during continent formation, lower continental crust, or lower oceanic crust.Mauna Kea tholeiitic lavas recovered from Hawaii Scientific Drilling Project (HSDP) can be divided into three groups based on their major element compositions: High-SiO2, Low-SiO2, and High-CaO groups. Detailed geochemical and isotopic studies have been focused on the High- and Low-SiO2 group lavas, and High-CaO lavas were not well studied because they were not included in the original reference suite samples. Here we report trace element compositions determined on a suite of High-CaO glasses, and use these data to constrain the petrogenesis of High-CaO lavas. When normalized to Low-SiO2 lavas, High-CaO lavas form a U-shaped trace element pattern. That is, High-CaO lavas are enriched in both the most (Nb, Th) and the least (Sc, V) incompatible elements. This trace element difference is best explained if High-CaO parental magma represents a mixture of low degree partial melt of the Low-SiO2 mantle source and a mafic cumulate component. This mafic cumulate must be clinopyroxene-rich, and it could be delaminated mafic cumulate formed under arcs during continent formation, lower continental crust, or lower oceanic crust.

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.

Implications for Core Formation of the Earth from High Pressure-Temperature Au Partitioning Experiments

NASA Technical Reports Server (NTRS)

Danielson, L. R.; Sharp, T. G.; Hervig, R. L.

2005-01-01

Siderophile elements in the Earth.s mantle are depleted relative to chondrites. This is most pronounced for the highly siderophile elements (HSEs), which are approximately 400x lower than chondrites. Also remarkable is the relative chondritic abundances of the HSEs. This signature has been interpreted as representing their sequestration into an iron-rich core during the separation of metal from silicate liquids early in the Earth's history, followed by a late addition of chondritic material. Alternative efforts to explain this trace element signature have centered on element partitioning experiments at varying pressures, temperatures, and compositions (P-T-X). However, first results from experiments conducted at 1 bar did not match the observed mantle abundances, which motivated the model described above, a "late veneer" of chondritic material deposited on the earth and mixed into the upper mantle. Alternatively, the mantle trace element signature could be the result of equilibrium partitioning between metal and silicate in the deep mantle, under P-T-X conditions which are not yet completely identified. An earlier model determined that equilibrium between metal and silicate liquids could occur at a depth of approximately 700 km, 27(plus or minus 6) GPa and approximately 2000 (plus or minus 200) C, based on an extrapolation of partitioning data for a variety of moderately siderophile elements obtained at lower pressures and temperatures. Based on Ni-Co partitioning, the magma ocean may have been as deep as 1450 km. At present, only a small range of possible P-T-X trace element partitioning conditions has been explored, necessitating large extrapolations from experimental to mantle conditions for tests of equilibrium models. Our primary objective was to reduce or remove the additional uncertainty introduced by extrapolation by testing the equilibrium core formation hypothesis at P-T-X conditions appropriate to the mantle.

Mid-Tertiary (25-21 Ma) lamprophyres in NW Mexico derived from subduction-modified subcontinental lithospheric mantle in an extensional backarc environment following steepening of the Benioff zone

NASA Astrophysics Data System (ADS)

Orozco-Garza, Alberto; Dostal, Jaroslav; Keppie, J. Duncan; Paz-Moreno, Francisco A.

2013-04-01

The mid-Tertiary lamprophyre dike swarm (~ 8 km × 2.5 km in size) from Hermosillo (Sonora, NW Mexico) has calc-alkaline characteristics and includes NNW-striking, amphibole-phyric spessartite (~ 85% of the swarm) and NNE-striking, phlogopite-phyric kersantite. The 40Ar/39Ar geochronology of amphibole and phlogopite gives overlapping plateau ages ranging from 25 to 21 Ma. Although all the lamprophyres are enriched in incompatible elements and display negative Nb-Ta and Ti anomalies on the primitive mantle-normalized plots, kersantite has higher K/Na, La/Yb, P, Ti and incompatible trace elements (e.g., Zr) compared to spessartite. The lamprophyres have radiogenic Sr and Nd isotopic signatures (87Sr/86Sr ~ 0.7057-0.7065 and ɛNd ~- 1 to - 2.3) suggesting derivation from the subcontinental lithospheric mantle that was previously modified by subduction-related fluids. This mantle is similar to that beneath the southern Grenvillian orogen, which has younger TDM ages than the 1.6-1.7 Ga TDM ages of the Caborca block. The lamprophyric magmas were generated at various mantle depths at the southwestern edge of North America. Intrusion of the lamprophyres was synchronous with extension that produced normal faults and core complexes with WSW-vergence. Extension occurred immediately following steepening of the Benioff zone, during which the magmatic arc migrated from east to west of Hermosillo, and the lamprophyres were intruded just behind the contemporaneous arc.

Petrological Constraints on Melt Generation Beneath the Asal Rift (Djibouti)

NASA Astrophysics Data System (ADS)

Pinzuti, P.; Humler, E.; Manighetti, I.; Gaudemer, Y.; Bézos, A.

2010-12-01

The temporal evolution of the mantle melting processes in the Asal Rift is evaluated from the chemical composition of 95 lava flows sampled along 10 km of the rift axis and 8 km off-axis (that is for the last 650 ky). The major element composition and the trace element ratios of aphyric basalts across the Asal Rift show a symmetric pattern relative to the rift axis and preserved a clear signal of mantle melting depth variations. FeO, Fe8.0, Sm/YbN and Zr/Y increase, whereas SiO2 and Lu/HfN decrease from the rift axis to the rift shoulders. These variations are qualitatively consistent with a shallower melting beneath the rift axis than off-axis and the data show that the melting regime is inconsistent with a passive upwelling model. In order to quantify the depth range and extent of melting, we invert Na8.0 and Fe8.0 contents of basalts based on a pure active upwelling model. Beneath the rift axis, melting paths are shallow, from 60 to 30 km. These melting paths are consistent with adiabatic melting in normal-temperature asthenosphere, beneath an extensively thinned mantle lithosphere. In contrast, melting on the rift shoulders occurred beneath a thick mantle lithosphere and required mantle solidus temperature 180°C hotter than normal (melting paths from 110 to 75 km). The calculated rate of lithospheric thinning is high (6.0 cm yr-1) and could explain the survival of a metastable garnet within the mantle at depth shallower than 90 km beneath the modern Asal Rift.

Evaluating the cause(s) of Ti, Ta, and Nb (TITAN) enrichment in ocean island basalts using LA-ICP-MS

NASA Astrophysics Data System (ADS)

Lyakov, J.; Durkin, K.; Hirsch, L.; Peters, B.; Hattingh, R.; Day, J. M.

2017-12-01

Titanium, Ta, and Nb (TITAN) enrichments in some ocean island basalt (OIB) lavas have been attributed to mantle source, or to partial melting and fractional crystallization Iprocesses. TITAN anomalies in the mantle sources of OIB would imply these trace elements can be used to track mantle heterogeneity in a manner similar to some isotopic tracers (e.g., He, Os, W), whereas a petrogenetic process to account for TITAN anomalies would be more prosaic. To further evaluate this issue, we have performed laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) of phenocryst phases and matrix on petrographically well-characterized polished-sections of OIB samples. These samples come from five ocean island archipelagos (Canary Islands, the Azores, Samoa, Tubuai'i, Réunion), and are used to assess the citing of Ti, Ta, Nb and associated trace-elements within bulk-rocks. We find poorly-defined but broadly positive correlations between olivine and clinopyroxene modal abundance and Ta/Ta*, Nb/Nb*, but no correlation with Ti/Ti* (where, for example, Ti/Ti* is the primitive mantle normalized ratio, written as: Ti/√[Sm × Tb]). Abundances of olivine and clinopyroxene with samples spanned a wide-range, from 0-70 modal %. We determined trace-element abundances by LA-ICP-MS in a sub-set of samples for major (olivine, clinopyroxene) and minor (e.g., magnetite) phenocryst phases, and for the typically vitrophyric to partly crystallized matrices of samples. Modal reconstruction relative to the bulk rock are broadly similar, although the Ta/Ta*, Nb/Nb* and, especially Ti/Ti* anomalies cannot always be reproduced, especially if Fe-Ti oxide phases were not analyzed due to their limited presence within polished sections. LA-ICP-MS analyses reveal that, while TITAN anomalies are dominantly preserved in the matrix and oxide phases, the role of fractional crystallization of olivine and clinopyroxene is a controlling factor in the magnitude of TITAN anomaly generated. Our results support suggestions that Ti, Ta and Nb are affected by partial melting, assimilation and fractional crystallization processes during magma evolution, generating more prominent TITAN anomalies in volcanic samples than their mantle sources.

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.

Trace element analyses of fluid-bearing diamonds from Jwaneng, Botswana

NASA Astrophysics Data System (ADS)

Schrauder, Marcus; Koeberl, Christian; Navon, Oded

1996-12-01

Fibrous diamonds from Botswana contain abundant micro-inclusions, which represent syngenetic mantle fluids under high pressure. The major element composition of the fluids within individual diamonds was found to be uniform, but a significant compositional variation exists between different diamond specimens. The composition of the fluids varies between a carbonatitic and a hydrous endmember. To constrain the composition of fluids in the mantle, the trace element contents of thirteen micro-inclusion-bearing fibrous diamonds from Botswana was studied using neutron activation analysis. The concentrations of incompatible elements (including K, Na, Br, Rb, Sr, Zr, Cs, Ba, Hf, Ta, Th, U, and the LREEs) in the fluids are higher than those of mantle-derived rocks and melt inclusions. The compatible elements (e.g., Cr, Co, Ni) have abundances that are similar to those of the primitive mantle. The concentrations of most trace elements decrease by a factor of two from the carbonate-rich fluids to the hydrous fluids. Several models may explain the observed elemental variations. Minerals in equilibrium with the fluid were most likely enriched in incompatible elements, which does not agree with derivation of the fluids by partial melting of common peridotites or eclogites. Fractional crystallization of a kimberlite-like magma at depth may yield carbonatitic fluids with low mg numbers (atomic ratio [Mg/(Mg+Fe)]) and high trace element contents. Fractionation of carbonates and additional phases (e.g., rutile, apatite, zircon) may, in general, explain the concentrations of incompatible elements in the fluids, which preferably partition into these phases. Alternatively, mixing of fluids with compositions similar to those of the two endmembers may explain the observed variation of the elemental contents. The fluids in fibrous diamonds might have equilibrated with mineral inclusions in eclogitic diamonds, while peridotitic diamonds do not show evidence of interaction with these fluids. The chemical composition of the fluids in fibrous diamonds indicates that, at p, T conditions that are characteristic for diamond formation, carbonatitic and hydrous fluids are efficient carriers of incompatible elements.

Petrogenesis of the ∼500 Ma Fushui mafic intrusion and Early Paleozoic tectonic evolution of the Northern Qinling Belt, Central China

NASA Astrophysics Data System (ADS)

Shi, Yu; Pei, Xiaoli; Castillo, Paterno R.; Liu, Xijun; Ding, Haihong; Guo, Zhichao

2017-06-01

The Fushui mafic intrusion in the Qinling orogenic belt (QOB) is composed of meta-gabbro, meta-gabbro-diorite, diorite, and syenite. Most of these rocks are metamorphosed under the upper greenschist facies to lower amphibolite facies metamorphism. Zircon separates from eight samples have LA-ICP-MS U-Pb ages of 497-501 Ma which are taken to be the emplacement age of magmas that formed the Fushui intrusion. Most of the zircon grains exhibit negative εHf values, correspond to TDM2 model ages of late Paleoproterozoic-early Mesoproterozoic or Neoproterozoic and suggest that the mafic rocks were most probably derived from mafic melts produced by partial melting of a previously metasomatized lithospheric mantle. The intrusion is not extensively contaminated by crustal materials and most chemical compositions of rocks are not modified during the greenschist to amphibolite-facies metamorhism. Rocks from the intrusion have primitive mantle-normalized trace element patterns with significant enrichment in light-REE and large ion lithophile elements (LILE) and depletion in high field-strength elements (HFSE). On the basis of the trace element contents, the Fushui intrusion was derived from parental magmas generated by <10% partial melting of both phlogopite-lherzolite and garnet-lherzolite mantle sources. These sources are best interpreted to be in a subduction-related arc environment and have been modified by fluids released from a subducting slab. The formation of the Fushui intrusion was related to the subduction of the Paleotethyan Shangdan oceanic lithosphere at ∼500 Ma.

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.

A high-pyrite semianthracite of Late Permian age in the Songzao Coalfield, southwestern China: Mineralogical and geochemical relations with underlying mafic tuffs

USGS Publications Warehouse

Dai, S.; Wang, X.; Chen, W.; Li, D.; Chou, C.-L.; Zhou, Y.; Zhu, Chen; Li, H.; Zhu, Xudong; Xing, Y.; Zhang, W.; Zou, J.

2010-01-01

The No. 12 Coal (Late Permian) in the Songzao Coalfield, Chongqing, southwestern China, is characteristically high in pyrite and some trace elements. It is uniquely deposited directly above mafic tuff beds. Samples of coal and tuffs have been studied for their mineralogy and geochemistry using inductively coupled plasma-mass spectrometry, X-ray fluorescence, plasma low-temperature ashing plus powder X-ray diffraction, and scanning electron microscopy equipped with energy-dispersive X-ray analysis.The results show that the minerals of the No. 12 Coal are mainly composed of pyrite, clay minerals (kaolinite, chamosite, and illite), ankerite, calcite, and trace amounts of quartz and boehmite. Kaolinite and boehmite were mainly derived from sediment source region of mafic tuffs. Chamosite was formed by the reaction of kaolinite with Fe-Mg-rich fluids during early diagenesis. The high pyrite (Sp,d=8.83%) in the coal was related to marine transgression over peat deposits and abundant Fe derived from the underlying mafic tuff bed. Ankerite and calcite were precipitated from epigenetic fluids.Chemical compositions of incompatible elements indicate that the tuffs were derived from enriched mantle and the source magmas had an alkali-basalt character. Compared to other coals from the Songzao Coalfield and common Chinese coals, the No. 12 Coal has a lower SiO2/Al2O3 (1.13) but a higher Al2O3/Na2O (80.1) value and is significantly enriched in trace elements including Sc (13.5??g/g), V (121??g/g), Cr (33.6??g/g), Co (27.2??g/g), Ni (83.5??g/g), Cu (48.5??g/g), Ga (17.3??g/g), Y (68.3??g/g), Zr (444??g/g), Nb (23.8??g/g), and REE (392??g/g on average). Above mineralogical compositions, as well as similar ratios of selected elements (e.g., SiO2/Al2O3 and Al2O3/Na2O) and similar distribution patterns of incompatible elements (e.g., the mantle-normalized diagram for incompatible elements and chondrite-normalized diagram for rare earth elements) of coal and tuff, indicated that enriched trace elements above were largely derived from mafic tuffs, in addition to a minor amount from the Kandian Oldland. ?? 2010 Elsevier B.V.

The Middle Triassic evolution of the Bangong-Nujiang Tethyan Ocean: evidence from analyses of OIB-type basalts and OIB-derived phonolites in northern Tibet

NASA Astrophysics Data System (ADS)

Fan, Jian-Jun; Li, Cai; Liu, Jin-Heng; Wang, Ming; Liu, Yi-Ming; Xie, Chao-Ming

2017-12-01

In this paper, we present new major and trace element chemical data for the basalts and phonolites of the Nare ocean island fragment (NaOI), as well as zircon U-Pb age data and Hf isotope compositions for the NaOI phonolites in the middle segment of the Bangong-Nujiang Suture Zone, northern Tibet. Our aim is to assess the genesis of these rocks and to reconstruct the Middle Triassic evolution of the Bangong-Nujiang Tethyan Ocean (BNTO). The NaOI retains an ocean island-type double-layered structure comprising a basaltic basement and an oceanic sedimentary cover sequence (conglomerate and limestone, the latter accompanied by layers of erupted phonolite near the top of the sequence). The basalts in the NaOI are enriched in light rare earth elements and high field strength elements (Nb, Ta, Zr, Hf, and Ti), and they exhibit chondrite-normalized REE patterns and primitive mantle-normalized trace element patterns similar to those of ocean island basalts. Taking into consideration their high Dy/Yb, Sm/Yb, and La/Sm ratios, we conclude that the NaOI basalts were derived from the partial melting of garnet peridotite in the mantle. The NaOI phonolites have LREE-enriched chondrite-normalized REE patterns with negative Eu anomalies (Eu/Eu* = 0.41-0.43) and primitive mantle-normalized trace element patterns with enrichments in Nb, Ta, Zr, and Hf, and depletions in Ba, U, Sr, P, and Ti. Given the high contents of Nb (172-256 ppm), Ta (11.8-16.0 ppm), Zr (927-1117 ppm), and Hf (20.8-26.9 ppm), and the very low contents of MgO (0.11-0.25 wt%), the very low Mg# values (5-10), and the near-zero contents of Cr (1.27-7.59 ppm), Ni (0.43-7.19 ppm), and Co (0.11-0.38 ppm), and the small and homogeneously positive ɛ Hf(t) values (+ 4.9 to + 9.5), we infer that the NaOI phonolites were formed by the fractional crystallization of an OIB-derived mafic parent magma. The phonolites of the NaOI contain zircons that yielded U-Pb ages of 239 and 242 Ma, indicating that the NaOI formed during the Middle Triassic. These data, combined with data from modern ocean islands (e.g., Canary Islands, Cape Verde, Fernando de Noronha, Tristan da Cunha, and Gough in the Atlantic Ocean, and Society and Austral-Cook in the Pacific Ocean), lead us to infer that the BNTO was open for a long time before the Middle Triassic, and that the ocean had already developed into a mature ocean with a thick oceanic lithosphere by at least the Middle Triassic.

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.

The petrogenesis of island arc basalts from Gunung Slamet volcano, Indonesia: Trace element and 87Sr /86Sr contraints

NASA Astrophysics Data System (ADS)

Vukadinovic, Danilo; Nicholls, Ian A.

1989-09-01

Selected major and trace elements, rare earth element (REE) and 87Sr /86Sr data are presented for arc basalts from Gunung Slamet volcano, Java, Indonesia. On the basis of stratigraphy, trace element content, Zr/Nb, and 87Sr /86Sr ratios, Slamet basalts can be broadly categorized into high abundance magma (HAM) and low abundance magma (LAM) types. Provided the quantities of 'immobile' trace elements (in aqueous systems) such as Nb, Hf and Zr in the mantle wedge and ensuing magmas are unaffected by additions from subducted lithosphere or overlying arc crust, a model may be developed whereby LAM are generated by higher degrees of melting in the mantle wedge (13%) compared to HAM (7%). Hf/Nb or Zr/Nb ratio systematics indicate that prior to metasomatism by the underlying lithosphere, the Slamet mantle wedge was similar in chemical character to transitional-MORB source mantle. Conversely, examination of immobile/mobile incompatible trace element ratios (IMITER) provide clues to the nature of the metasomatizing agent, most likely derived from the subducted slab (basalts and sediments). HAM have constant IMITER ( e.g.Nb/U, Zr/K), whereas LAM show a negative correlation between IMITER and 87Sr /86Sr . Metasomatism of the mantle wedge was modelled by interaction with either a slab-derived-melt or -aqueous fluid. Yb/Sr and 87Sr /86Sr ratios from Slamet basalts and oceanic sediments suggest that 'bulk' mixing of the latter into the mantle wedge is unlikely. Instead, sediments probably interact with overlying mantle in the same way that subducted basalts do-either as melts or fluids. In the case of slab-derived melts mixing with 'pristine' mantle, good agreement with back-calculated values for HAM and LAM sources can be achieved only if a residual phase such as rutile persists in the subducting lithosphere. In the case of fluids, excellent agreement with back-calculated values is obtained for all elements except heavy REE. It is tentatively suggested that aqueous slab-derived fluids, relatively rich in mobile incompatible elements, are the probable metasomatizing agent responsible for the chemical characteristics, particularly low IMITER, of Slamet and other island arc basalts (IAB). Because the mobilities/solubilities of Sr in high pressure and temperature fluids are poorly known, the modelled subduction fluids are not necessarily efficient at raising 87Sr /86Sr in the overlying mantle wedge. As a result, positive correlations between e.g.Ba/La vs. 87Sr /86Sr need not be observed in arc suites, especially if the relative mobilities of Sr, Ba, and La are dependent upon intensive parameters during metasomatism. Assimilation of arc crust by uprising magmas (up to ~14% of crustal Sr) can account for the range of 87Sr /86Sr in HAM. However, calculating the amounts of arc crustal assimilation by uprising magmas is poorly constrained since such modelling is highly dependent upon previous estimates of the degree of metasomatism undergone by the mantle wedge.

High-K calc-alkaline magmatism at the Archaean-Proterozoic boundary: implications for mantle metasomatism and continental crust petrogenesis. Example of the Bulai pluton (Central Limpopo Belt, South Africa)

NASA Astrophysics Data System (ADS)

Laurent, Oscar; Martin, Hervé; Doucelance, Régis; Moyen, Jean-François; Paquette, Jean-Louis

2010-05-01

The Neoarchaean Bulai pluton, intrusive within the supracrustal granulites of the Central Limpopo Belt (Limpopo Province, South Africa) is made up of large volumes of porphyritic granodiorites with subordinate enclaves and dykes which have monzodioritic and charno-enderbitic compositions. New U-Pb LA-ICP-MS dating on separated zircons yielded pluton emplacement ages ranging between 2.60 and 2.63 Ga, which are slightly older than previous proposed ages (~ 2.57-2.61 Ga). The whole-rock major- and trace-element composition of the Bulai pluton evidences unequivocal affinities with "high-Ti" late-Archaean sanukitoids. It belongs to a high-K calc-alkaline differentiation suite, with metaluminous affinities (0.7 < A/CNK < 1) and relatively high Mg# (0.4-0.6). These rocks have "juvenile" affinities, such as eNd ranging between -0.5 and 0.5, and in addition, are very rich in all incompatible trace elements, which is particularly obvious in monzodioritic enclaves and enderbites where primitive mantle-normalized LILE and LREE contents are up to 300. These characteristics point to an enriched mantle source for the Bulai batholith. Chondrite normalized, REE patterns are strongly fractionated ([La/Yb]N ~ 25-80), mainly due to high LREE contents (LaN ~ 250-630), and chiefly high HFSE contents (Nb ~ 15-45 ppm ; up to 770 ppm Zr) indicate that the metasomatic agent is a silicic melt rather than a hydrous fluid. Moreover, based on high Nb/Ta, Th/Rb, La/Rb and low Sr/Nd and Ba/La, we suggest that the metasomatic agent is a granitic melt generated by melting of terrigenous sediments. Interactions of this melt with mantle peridotites implies that sediments are located under a mantle slice; geometry which is easily achieved in subduction zone settings. This conclusion is supported by the fact that Bulai trace element patterns are very similar to those of sub-actual potassic magmas generated in magmatic arc environments by interactions between mantle and terrigenous sediments (e.g. Sunda arc). Geochemical modeling indicates that the mafic facies of the Bulai pluton can be achieved by a two-stage process: 1) a liquid produced by melting of subducted terrigenous sediment is entirely consumed by metasomatic reactions with mantle peridotites, producing a metasomatic amphibole- and phlogopite-bearing assemblage ; 2) Low-degree melting of this metasomatized mantle gives rise to magmas with the same trace element signature than the Bulai mafics. Such a petrogenetic model is consistent with previous geochemical and experimental study about sanukitoids, which concluded that these magmas result of interactions between slab melts and the overlying mantle wedge. Subsequently, at crustal levels, the Bulai monzodiorite not only underwent significant fractional crystallization, but also induce melting of the host rocks, and mixed with the resulting felsic crustal magmas. Such that it can be concluded that the whole Bulai suite can be derived through AFC processes. Our geochemical study failed in demonstrating any significant role played by melting of subducted metabasalts, which contrasts to Archaean times, and would point to lower thermal regimes as the wet solidus of metasediments is ~ 50 to 100°C lower than that of metabasalts at slab pressures. In addition the fact that the whole felsic melts were consumed by reaction with peridotite is indicative of lower degrees of melting of the slab compared with Archaean processes. Both conclusions imply that the geodynamic changes that took place at the Archaean-Proterozoic transition and witnessed by sanukitoid-related rocks are the result of progressive and global cooling of Earth.

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).

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.

Trace element and strontium isotope characteristics of volcanic rocks from Isla Tortuga: a young seamount in the Gulf of California

USGS Publications Warehouse

Batiza, Rodey; Futa, K.; Hedge, C.E.

1979-01-01

Isla Tortuga is a small isolated central volcano which is located near an actively spreading trough in the Gulf of California. The basalt lavas from Tortuga which have the highest Mg/Fe and Ni contents have trace element abundances and ratios and 87Sr/86Sr which are similar to those of mid-ocean ridge tholeiite. The major element, rare earth element and Sr abundances of fractionated tholeiite (low Mg/Fe) and tholeiitic andesite of Tortuga are consistent with an origin by closed-system fractional crystallization. This hypothesis is not supported by K, Na, Rb and Ba abundances in the lavas nor by their variable 87Sr/86Sr (0.7024-0.7035). It is proposed that the apparent decoupling of light rare earth elements, other incompatible trace elements and 87Sr/86Sr is due to contamination of some Tortuga magmas while they are fractionated in a high-level crustal magma chamber. The mantle source of least-contaminated, high Mg/Fe basalt lavas of Tortuga is similar, although not identical to the source of normal mid-ocean ridge tholeiite; significant differences exist. The reasons for these differences are not yet known. ?? 1979.

On the nature and origin of garnet in highly-refractory Archean lithosphere: implications for continent stabilisation

NASA Astrophysics Data System (ADS)

Gibson, Sally

2014-05-01

The nature and timescales of garnet formation in the Earth's subcontinental lithospheric mantle (SCLM) are important to our understanding of how this rigid outer shell has evolved and stabilised since the Archean. Nevertheless, the widespread occurrence of pyrope garnet in the sub-cratonic mantle remains one of the 'holy grails' of mantle petrology. The paradox is that garnet often occurs in mantle lithologies (dunites and harzburgites) which represent residues of major melting events (up to 40 %) whereas experimental studies on fertile peridotite suggest this phase should be exhausted by <20 % melting. Furthermore, garnets commonly found in mantle peridotite suites have diverse compositions that are typically in equilibrium with high-pressure, small-fraction, mantle melts suggesting they formed as a result of enrichment of the lithospheric mantle following cratonisation. This refertilisation -- which typically involves addition of Fe, incompatible trace elements and volatiles -- affects the lower 30 km of the lithosphere and potentially leads to negative buoyancy and destabilisation. Pyrope garnets found in mantle xenoliths from the eastern margin of the Tanzanian Craton (Lashaine) have diverse compositions and provide major constraints on how the underlying deep (120 to 160 km) mantle stabilised and evolved during the last 3 billion years. The garnets display systematic trends from ultra-depleted to enriched compositions that have not been recognised in peridotite suites from elsewhere (Gibson et al., 2013). Certain harzburgite members of the xenolith suite contain the first reported occurrence of pyrope garnets with rare-earth element (REE) patterns similar to hypothetical garnets proposed by Stachel et al. (2004) to have formed in the Earth's SCLM during the Archean, prior to metasomatism. These rare ultra-depleted low-Cr garnets occur in low temperature (~1050 oC) xenoliths derived from depths of ~120 km and coexist in chemical and textural equilibrium with highly-refractory olivine (Fo95.4) and orthopyroxene (Mg#=96.4). These phases are all more magnesian than generally encountered in global samples of depleted mantle, i.e. harzburgites and diamond inclusion suites. The Tanzanian ultra-depleted garnets form interconnecting networks ('necklaces') around grains of orthopyroxene, which is of key importance to their origin. This close spatial relationship of garnet and orthopyroxene together with the major, trace and REE contents of the ultra-depleted garnets, are consistent with an origin by isochemical exsolution. The significance of ultra-depleted low-Cr garnets has not previously been recognised in global suites of mantle xenoliths or diamond inclusions: they appear to have been overlooked, primarily because of their unusual pre-metasomatic compositions. We believe they are rare because the low concentrations of trace elements make them readily susceptible to geochemical overprinting. This highly-refractory low-density peridotite may be common in the 'shallow' SCLM but is not normally brought to the surface by ascending melts, which tend to metasomatise and preferentially sample their source regions. The modal abundance of garnet formed by isochemical exsolution from orthopyroxene in sub-cratonic mantle is unclear but may prove to be an important consideration in isopycnic models related to the long-term stability of the Earth's continental lithosphere, e.g. Lee et al. (2011). Gibson, S. A., McMahon, S. C., Day, J. A. & Dawson, J. B. (2013). Highly Refractory Lithospheric Mantle beneath the Tanzanian Craton: Evidence from Lashaine Pre-metasomatic Garnet-bearing Peridotites. J. Petrol. doi:10.1093/petrology/egt020 Stachel, T., Aulbach, A., Brey, G.P., Harris, J.W., Leost, I., Tappert, R. & Viljoen, K.S. (2004). The trace element composition of silicate inclusions in diamonds: a review. Lithos 77, 1-19 Lee, C.-T., Luffi, P. & Chin, E. J. (2011). Building and Destroying Continental Mantle. Annu. Rev. Earth Planet. Sci. 39, 59-90

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.

Formation and evolution of a metasomatized lithospheric root at the motionless Antarctic plate: the case of East Island, Crozet Archipelago (Indian Ocean)

NASA Astrophysics Data System (ADS)

Meyzen, Christine; Marzoli, Andrea; Bellieni, Giuliano; Levresse, Gilles

2016-04-01

Sitting atop the nearly stagnant Antarctic plate (ca. 6.46 mm/yr), the Crozet archipelago midway between Madagascar and Antarctica constitutes a region of unusually shallow (1543-1756 m below sea level) and thickened oceanic crust (10-16.5 km), high geoid height, and deep low-velocity zone, which may reflect the surface expression of a mantle plume. Here, we present new major and trace element data for Quaternary sub-aerial alkali basalts from East Island, the easterly and oldest island (ca. 9 Ma) of the Crozet archipelago. Crystallization at uppermost mantle depth and phenocryst accumulation have strongly affected their parental magma compositions. Their trace element patterns show a large negative K anomaly relative to Ta-La, moderate depletions in Rb and Ba with respect to Th-U, and heavy rare earth element (HREE) depletions relative to light REE. These characteristics allow limits to be placed upon the composition and mineralogy of their mantle source. The average trace element spectrum of East Island basalts can be matched by melting of about 2 % of a garnet-phlogopite-bearing peridotite source. The stability field of phlogopite restricts melting depth to lithospheric levels. The modelled source composition requires a multistage evolution, where the mantle has been depleted by melt extraction before having been metasomatized by alkali-rich plume melts. The depleted mantle component may be sourced by residual mantle plume remnants stagnated at the melting locus due to a weak lateral flow velocity inside the melting regime, whose accumulation progressively edifies a depleted lithospheric root above the plume core. Low-degree alkali-rich melts are likely derived from the plume source. Such a mantle source evolution may be general to both terrestrial and extraterrestrial environments where the lateral component velocity of the mantle flow field is extremely slow.

Tracking the Martian Mantle Signature in Olivine-Hosted Melt Inclusions of Basaltic Shergottites Yamato 980459 and Tissint

NASA Technical Reports Server (NTRS)

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

2014-01-01

The Martian shergottite meteorites are basaltic to lherzolitic igneous rocks that represent a period of relatively young mantle melting and volcanism, approximately 600-150 Ma (e.g. [1,2]). Their isotopic and elemental composition has provided important constraints on the accretion, evolution, structure and bulk composition of Mars. Measurements of the radiogenic isotope and trace element concentrations of the shergottite meteorite suite have identified two end-members; (1) incompatible trace element enriched, with radiogenic Sr and negative epsilon Nd-143, and (2) incompatible traceelement depleted, with non-radiogenic Sr and positive epsilon 143-Nd(e.g. [3-5]). The depleted component represents the shergottite martian mantle. The identity of the enriched component is subject to debate, and has been proposed to be either assimilated ancient martian crust [3] or from enriched domains in the martian mantle that may represent a late-stage magma ocean crystallization residue [4,5]. Olivine-phyric shergottites typically have the highest Mg# of the shergottite group and represent near-primitive melts having experienced minimal fractional crystallization or crystal accumulation [6]. Olivine-hosted melt inclusions (MI) in these shergottites represent the most chemically primitive components available to understand the nature of their source(s), melting processes in the martian mantle, and origin of enriched components. We present trace element compositions of olivine hosted melt inclusions in two depleted olivinephyric shergottites, Yamato 980459 (Y98) and Tissint (Fig. 1), and the mesostasis glass of Y98, using Secondary Ionization Mass Spectrometry (SIMS). We discuss our data in the context of understanding the nature and origin of the depleted martian mantle and the emergence of the enriched component.

Non-Destructive Trace Element Tomography Using Europe's Brightest Synchrotron Sources (ESRF-Grenoble, DESY-Hamburg) — Towards a Better Understanding of Martian Samples

NASA Astrophysics Data System (ADS)

Brenker, F. E.; Vincze, L.; Vekemans, B.; de Poulle, E.

2018-04-01

Synchrotron sources are valuable tools to measure the main and trace element content of extraterrestrial samples. The non-destructive measurements will allow to identify important geological processes within the martian mantle and crust.

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.

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.

Redox state of recycled crustal lithologies in the convective upper mantle constrained using oceanic basalt CO2-trace element systematics

NASA Astrophysics Data System (ADS)

Eguchi, J.; Dasgupta, R.

2017-12-01

Investigating the redox state of the convective upper mantle remains challenging as there is no way of retrieving samples from this part of the planet. Current views of mantle redox are based on Fe3+/∑Fe of minerals in mantle xenoliths and thermodynamic calculations of fO2 [1]. However, deep xenoliths are only recoverable from continental lithospheric mantle, which may have different fO2s than the convective oceanic upper mantle [1]. To gain insight on the fO2 of the deep parts of the oceanic upper mantle, we probe CO2-trace element systematics of basalts that have been argued to receive contributions from subducted crustal lithologies that typically melt deeper than peridotite. Because CO2 contents of silicate melts at graphite saturation vary with fO2 [2], we suggest CO2-trace element systematics of oceanic basalts which sample deep heterogeneities may provide clues about the fO2 of the convecting mantle containing embedded heterogeneities. We developed a new model to predict CO2 contents in nominally anhydrous silicate melts from graphite- to fluid-saturation over a range of P (0.05- 5 GPa), T (950-1600 °C), and composition (foidite-rhyolite). We use the model to calculate CO2 content as a function of fO2 for partial melts of lithologies that vary in composition from rhyolitic sediment melt to silica-poor basaltic melt of pyroxenites. We then use modeled CO2 contents in mixing calculations with partial melts of depleted mantle to constrain the fO2 required for partial melts of heterogeneities to deliver sufficient CO2 to explain CO2-trace element systematics of natural basalts. As an example, Pitcairn basalts, which show evidence of a subducted crustal component [3] require mixing of 40% of partial melts of a garnet pyroxenite at ΔFMQ -1.75 at 3 GPa. Mixing with a more silicic composition such as partial melts of a MORB-eclogite cannot deliver enough CO2 at graphite saturation, so in this scenario fO2 must be above the EMOG/D buffer at 4 GPa. Results suggest convecting upper mantle may be more oxidized than continental lithospheric mantle, and fO2 profiles of continental lithospheric mantle may not be applicable to convective upper mantle.[1] Frost, D, McCammon, C. 2008. An Rev E & P Sci. (36) p.389-420; [2] Holloway, J, et al. 1992. Eu J. Min. (4) p. 105-114; [3] Woodhead, J, Devey C. 1993. EPSL. (116) p. 81-99.

Metasomatized mantle as the source of Mid-Miocene-Quaternary volcanism in NW-Iranian Azerbaijan: Geochronological and geochemical evidence

NASA Astrophysics Data System (ADS)

Lechmann, Anna; Burg, Jean-Pierre; Ulmer, Peter; Guillong, Marcel; Faridi, Mohammad

2018-04-01

Middle Miocene to Quaternary volcanic rocks cover large areas of the Azerbaijan Province in NW Iran. This study reports two separate age clusters out of 23 new LA-ICP-MS U-Pb zircon ages: (1) Middle Miocene (16.2-10.6 Ma) and (2) Latest Miocene-Late Pleistocene (5.5-0.4 Ma). Major and trace element bulk rock geochemistry and initial Sr, Nd, Pb radiogenic isotope data on the dated rocks provide new constraints on the Mid-Miocene to Quaternary volcanism in this region. The analyses are distributed over a large compositional range from low-K to high-K calc-alkaline andesites and dacites/rhyolites to more alkaline trachybasalts and dacites with shoshonitic affinities. Chondrite-normalized REE patterns are steep with significant enrichment in LREE and low abundances of HREE indicating a garnet control. Plots of primitive mantle-normalized trace elements show negative Ti and Nb-Ta anomalies indicative of an arc signature. The wide compositional range and the ubiquitous presence of an arc signature reveal that the source mantle is heterogeneous and metasomatically altered. Sr, Nd and Pb radiogenic isotope data further point towards an enriched mantle source and/or crustal contamination. Crustal contamination is best recognized by inherited zircon cores, which yield Late Neoproterozoic to Early Cambrian ages typical for the Iranian basement. The occurrence of adakite-like compositions with elevated magnesium numbers, Cr and Ni concentrations argue against a fractionation-driven process but point to a subcrustal origin. Overall, the analyzed lavas show no spatial and temporal relation to a potential subduction zone, confirming the dated volcanics to be post-collisional and not related to singular processes such as slab retreat or delamination of a continuous lower crustal sliver. We propose three hypotheses to explain the reported disparity in distribution, age and composition and favour small-scale sublithospheric convection or incorporation of crustal material into the metasomatized mantle. The discovery of the late Miocene time gap is in line with previously advocated exhumation pulses and coincides with a major tectonic reorganization in the Arabian-Eurasian realm at this time.

Composition of the earth's upper mantle. II - Volatile trace elements in ultramafic xenoliths

NASA Technical Reports Server (NTRS)

Morgan, J. W.; Wandless, G. A.; Petrie, R. K.; Irving, A. J.

1980-01-01

Radiochemical neutron activation analysis was used to determine the nine volatile elements Ag, Bi, Cd, In, Sb, Se, Te, Tl, and Zn in 19 ultramafic rocks, consisting mainly of spinel and garnet lherzolites. A sheared garnet lherzolite, PHN 1611, may approximate undepleted mantle material and tends to have a higher volatile element content than the depleted mantle material represented by spinel lherzolites. Comparisons of continental basalts with PHN 1611 and of oceanic ridge basalts with spinel lherzolites show similar basalt: source material partition factors for eight of the nine volatile elements, Sb being the exception. The strong depletion of Te and Se in the mantle, relative to lithophile elements of similar volatility, suggests that 97% of the earth's S, Se and Te may be in the outer core.

Trace element behavior in hydrothermal experiments: Implications for fluid processes at shallow depths in subduction zones

NASA Astrophysics Data System (ADS)

You, C.-F.; Castillo, P. R.; Gieskes, J. M.; Chan, L. H.; Spivack, A. J.

1996-05-01

Chemical evaluation of fluids affected during progressive water-sediment interactions provides critical information regarding the role of slab dehydration and/or crustal recycling in subduction zones. To place some constraints on geochemical processes during sediment subduction, reactions between décollement sediments and synthetic NaCl-CaCl 2 solutions at 25-350°C and 800 bar were monitored in laboratory hydrothermal experiments using an autoclave apparatus. This is the first attempt in a single set of experiments to investigate the relative mobilities of many subduction zone volatiles and trace elements but, because of difficulties in conducting hydrothermal experiments on sediments at high P-T conditions, the experiments could only be designed for a shallow (˜ 10 km) depth. The experimental results demonstrate mobilization of volatiles (B and NH 4) and incompatible elements (As, Be, Cs, Li, Pb, Rb) in hydrothermal fluids at relatively low temperatures (˜ 300°C). In addition, a limited fractionation of light from heavy rare earth elements (REEs) occurs under hydrothermal conditions. On the other hand, the high field strength elements (HFSEs) Cr, Hf, Nb, Ta, Ti, and Zr are not mobile in the reacted fluids. The observed behavior of volatiles and trace elements in hydrothermal fluids is similar to the observed enrichment in As, B, Cs, Li, Pb, Rb, and light REEs and depletion in HFSEs in arc magmas relative to magmas derived directly from the upper mantle. Thus, our work suggests a link between relative mobilities of trace elements in hydrothermal fluids and deep arc magma generation in subduction zones. The experimental results are highly consistent with the proposal that the addition of subduction zone hydrous fluids to the subarc mantle, which has been depleted by previous melting events, can produce the unique characteristics of arc magmas. Moreover, the results suggest that deeply subducted sediments may no longer have the composition necessary to generate the other distinct characteristics, such as the B-δ 11 B and B- 10Be systematics, of arc lavas. Finally, the mobilization of B, Cs, Pb, and light REEs relative to heavy REEs in the hydrothermal fluids fractionate the ratios of B/Be, B/Nb, Cs/Rb, Pb/Ce, La/Ba and LREE/HREE, which behave conservatively during normal magmatic processes. These results demonstrate that the composition of slab-derived fluids has great implications for the recycling of elements; not only in arc magmas but also in mantle plumes.

Petrology and trace element geochemistry of the Honolulu volcanics, Oahu: implications for the oceanic mantle below Hawaii.

USGS Publications Warehouse

Clague, D.A.; Frey, F.A.

1982-01-01

These volcanic rocks are the products of small-volume, late-stage vents along rifts cutting the older massive Koolan tholeiitic shield on Oahu. Most of the lavas and tuffs have the geochemical features expected of near-primary magmas derived from a peridotite source with olivine Fo87-89, e.g. 100 Mg/(Mg + Fe2+) > 65, Ni > 250 p.p.m. and the presence of ultramafic mantle xenoliths at 18 of the 37 vents. Thus the geochemistry of the alkali olivine basalt, basanite, nephelinite and nepheline melilitite lavas and tuffs of these Honolulu volcanic rocks has been used to deduce the composition of their mantle source and the conditions under which they were generated by partial melting in the mantle. New major- and trace-element analyses for 31 samples are tabulated and indicate derivation by partial melting of a garnet (<10%) lherzolite source which was isotopically homogeneous and compositionally uniform for most major and trace elements, though apparently heterogeneous in TiO2, Zr, Hf, Nb and Ta (due perhaps to the low inferred degrees of melting which failed to exhaust the source in minor residual phases). In comparison with estimates of a primordial mantle composition and the mantle source of MORB, the garnet peridotite source of these Honolulu volcanics was increasingly enriched in the sequence heavy REE, Y, Tb, Ti, Sm, Zr and Hf, for which a multi-stage history is required. This composition differs from the source of the previously erupted tholeiitic shield, nor is it represented in the upper-mantle xenoliths in the lavas and tuff of the unit.-R.A.H.

Melting the lithosphere: Metasomes as a source for mantle-derived magmas

NASA Astrophysics Data System (ADS)

Rooney, Tyrone O.; Nelson, Wendy R.; Ayalew, Dereje; Hanan, Barry; Yirgu, Gezahegn; Kappelman, John

2017-03-01

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 an olivine-dominated source. Although there is mounting evidence 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. Here we present major and trace element analyses of 66 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 units identified in the later cinder cones and associated lava flows; (B) a clinopyroxene-phyric high Ti group (3.1-6.5 wt.% TiO2; 2.8-9.2 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. A characteristic negative K anomaly in primitive-mantle normalized diagrams, and Na2O > K2O, suggests a source rich in amphibole, devoid of olivine, and perhaps containing some carbonate and magnetite. While melt generation during rift development in Ethiopia is strongly correlated with the thermo-chemical anomalies associated with the African Superplume, thermobaric destabilization and melting of mantle metasomes may also contribute to lithospheric thinning. In regions impacted by mantle plumes, such melts may be critical to weakening of the continental lithosphere and the development of rifts.

Asthenospheric and lithospheric sources for Mesozoic dolerites from Liberia (Africa): trace element and isotopic evidence

NASA Astrophysics Data System (ADS)

Dupuy, C.; Marsh, J.; Dostal, J.; Michard, A.; Testa, S.

1988-01-01

Combined elemental, and Sr and Nd isotopic data are presented for Mesozoic dolerite dikes of Liberia (Africa) which are related to the initial stage of opening of the Atlantic Ocean. The large scatter of both trace element and isotopic data allows the identification of five groups of dolerites which cannot be related to each other by simple processes of mineral fractionation from a common source. On the contrary, the observed chemical and isotopic variation within some dolerites (Groups I and II) may result either from variable degrees of melting of an isotopically heterogeneous source or mixing between enriched and depleted oceanic type mantle. For the other dolerites (Groups III-V) mixing with a third mantle source with more radiogenic Sr and with element ratios characteristic of subduction environments is suggested. This third source is probably the subcontinental lithospheric mantle. Finally, no significant modification by interaction with continental crust is apparent in most of the analyzed samples.

Bernard J. Wood Receives 2013 Harry H. Hess Medal: Citation

NASA Astrophysics Data System (ADS)

Hofmann, Albrecht W.

2014-01-01

As Harry Hess recognized over 50 years ago, mantle melting is the fundamental motor for planetary evolution and differentiation. Melting generates the major divisions of crust mantle and core. The distribution of chemical elements between solids, melts, and gaseous phases is fundamental to understanding these differentiation processes. Bernie Wood, together with Jon Blundy, has combined experimental petrology and physicochemical theory to revolutionize the understanding of the distribution of trace elements between melts and solids in the Earth. Knowledge of these distribution laws allows the reconstruction of the source compositions of the melts (deep in Earth's interior) from their abundances in volcanic rocks. Bernie's theoretical treatment relates the elastic strain of the lattice caused by the substitution of a trace element in a crystal to the ionic radius and charge of this element. This theory, and its experimental calibrations, brought order to a literature of badly scattered, rather chaotic experimental data that allowed no satisfactory quantitative modeling of melting processes in the mantle.

Chemical composition of rocks and soils at Taurus-Littrow

NASA Technical Reports Server (NTRS)

Rose, H. J., Jr.; Cuttitta, F.; Berman, S.; Brown, F. W.; Carron, M. K.; Christian, R. P.; Dwornik, E. J.; Greenland, L. P.

1974-01-01

Seventeen soils and seven rock samples were analyzed for major elements, minor elements, and trace elements. Unlike the soils at previous Apollo sites, which showed little difference in composition at each collection area, the soils at Taurus-Littrow vary widely. Three soil types are evident, representative of (1) the light mantle at the South Massif, (2) the dark mantle in the valley, and (3) the surface material at the North Massif. The dark-mantle soils are chemically similar to those at Tranquillitatis. Basalt samples from the dark mantle are chemically similar although they range from fine to coarse grained. It is suggested that they originated from the same source but crystallized at varying depths from the surface.

Platinum group elements in a 3.5 Ga nickel-iron occurrence - Possible evidence of a deep mantle origin

NASA Technical Reports Server (NTRS)

Tredoux, Marian; Hart, Rodger J.; Lindsay, Nicholas M.; De Wit, Maarten J.; Armstrong, Richard A.

1989-01-01

This paper reports the results of new field observations and the geochemical analyses for the area of the Bon Accord (BA) (the Kaapvaal craton, South Africa) Ni-Fe deposit, with particular consideration given to the trace element, platinum-group element, and isotopic (Pb, Nd, and Os) compositions. On the basis of these data, an interpretation of BA is suggested, according to which the BA deposit is a siderophile-rich heterogeneity remaining in the deep mantle after a process of incomplete core formation. The implications of such a model for the study of core-mantle segregation and the geochemistry of the lowermost mantle are discussed.

The role of sulfides in the fractionation of highly siderophile and chalcophile elements during the formation of martian shergottite meteorites

NASA Astrophysics Data System (ADS)

Baumgartner, Raphael J.; Fiorentini, Marco L.; Lorand, Jean-Pierre; Baratoux, David; Zaccarini, Federica; Ferrière, Ludovic; Prašek, Marko K.; Sener, Kerim

2017-08-01

The shergottite meteorites are ultramafic to mafic igneous rocks whose parental magmas formed from partial melting of the martian mantle. This study reports in-situ laser ablation inductively coupled plasma mass spectrometry analyses for siderophile and chalcophile major and trace elements (i.e., Co, Ni, Cu, As, Se, Ag, Sb, Te, Pb, Bi, and the highly siderophile platinum-group elements, PGE: Os, Ir, Ru, Rh, Pt and Pd) of magmatic Fe-Ni-Cu sulfide assemblages from four shergottite meteorites. They include three geochemically similar incompatible trace element- (ITE-) depleted olivine-phyric shergottites (Yamato-980459, Dar al Gani 476 and Dhofar 019) that presumably formed from similar mantle and magma sources, and one distinctively ITE-enriched basaltic shergottite (Zagami). The sulfides in the shergottites have been variably modified by alteration on Earth and Mars, as well as by impact shock-shock related melting/volatilization during meteorite ejection. However, they inherit and retain their magmatic PGE signatures. The CI chondrite-normalized PGE concentration patterns of sulfides reproduce the whole-rock signatures determined in previous studies. These similarities indicate that sulfides exerted a major control on the PGE during shergottite petrogenesis. However, depletions of Pt (and Ir) in sulfide relative to the other PGE suggest that additional phases such discrete Pt-Fe-Ir alloys have played an important role in the concentration of these elements. These alloys are expected to have enhanced stability in reduced and FeO-rich shergottite magmas, and could be a common feature in martian igneous systems. A Pt-rich PGM was found to occur in a sulfide assemblage in Dhofar 019. However, its origin may be related to impact shock-related sulfide melting and volatilisation during meteorite ejection. In the ITE-depleted olivine-phyric shergottites, positive relationships exist between petrogenetic indicators (e.g., whole-rock Mg-number) and most moderately to strongly siderophile and chalcophile elements in sulfides. These variations extend to incompatible elements like Te and Pd. The whole-rock concentrations of Pd derived from mass-balance calculations decrease by one order of magnitude in the order Y-980459, DaG 476 and Dhofar 019, and broadly overlap the trends in previously published whole-rock analyses. Mantle heterogeneities, and the timing of sulfide saturation as function of mantle melting and/or magma fractionation following ascent from the mantle, may have been the controlling factors of the siderophile and chalcophile element systematics in the analyzed shergottites.

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.

Trace element and isotopic composition of apatite in carbonatites from the Blue River area (British Columbia, Canada) and mineralogy of associated silicate rocks

NASA Astrophysics Data System (ADS)

Mitchell, Roger; Chudy, Thomas; McFarlane, Christopher R. M.; Wu, Fu-Yuan

2017-08-01

Apatites from the Verity, Fir, Gum, Howard Creek and Felix carbonatites of the Blue River (British Columbia, Canada) area have been investigated with respect to their paragenesis, cathodoluminescence, trace element and Sr-Nd isotopic composition. Although all of the Blue River carbonatites were emplaced as sills prior to amphibolite grade metamorphism and have undergone deformation, in many instances magmatic textures and mineralogy are retained. Attempts to constrain the U-Pb age of the carbonatites by SIMS, TIMS and LA-ICP-MS studies of zircon and titanite were inconclusive as all samples investigated have experienced significant Pb loss during metamorphism. The carbonatites are associated with undersaturated calcite-titanite amphibole nepheline syenite only at Howard Creek although most contain clasts of disaggregated phoscorite-like rocks. Apatite from each intrusion is characterized by distinct, but wide ranges, in trace element composition. The Sr and Nd isotopic compositions define an array on a 87Sr/86Sr vs²Nd diagram at 350 Ma indicating derivation from depleted sub-lithospheric mantle. This array could reflect mixing of Sr and Nd derived from HIMU and EM1 mantle sources, and implies that depleted mantle underlies the Canadian Cordillera. Although individual occurrences of carbonatites in the Blue River region are mineralogically and geochemically similar they are not identical and thus cannot be considered as rocks formed from a single batch of parental magma at the same stage of magmatic evolution. However, a common origin is highly probable. The variations in the trace element content and isotopic composition of apatite from each occurrence suggest that each carbonatite represents a combination of derivation of the parental magma(s) from mineralogically and isotopically heterogeneous depleted mantle sources coupled with different stages of limited differentiation and mixing of these magmas. We do not consider these carbonatites as primary direct partial melts of the sub-lithospheric mantle which have ascended from the asthenosphere without modification of their composition.

Geochemistry of Woranso-Mille Pliocene basalts from west-central Afar, Ethiopia: Implications for mantle source characteristics and rift evolution

NASA Astrophysics Data System (ADS)

Alene, Mulugeta; Hart, William K.; Saylor, Beverly Z.; Deino, Alan; Mertzman, Stanley; Haile-Selassie, Yohannes; Gibert, Luis B.

2017-06-01

The Woranso-Mille (WORMIL) area in the west-central Afar, Ethiopia, contains several Pliocene basalt flows, tuffs, and fossiliferous volcaniclastic beds. We present whole-rock major- and trace-element data including REE, and Sr-Nd-Pb isotope ratios from these basalts to characterize the geochemistry, constrain petrogenetic processes, and infer mantle sources. Six basalt groups are distinguished stratigraphically and geochemically within the interval from 3.8 to 3 Ma. The elemental and isotopic data show intra- and inter-group variations derived primarily from source heterogeneity and polybaric crystallization ± crustal inputs. The combined Sr-Nd-Pb isotope data indicate the involvement of three main reservoirs: the Afar plume, depleted mantle, and enriched continental lithosphere (mantle ± crust). Trace element patterns and ratios further indicate the basalts were generated from spinel-dominated shallow melting, consistent with significantly thinned Pliocene lithosphere in western Afar. The on-land continuation of the Aden rift into western Afar during the Pliocene is reexamined in the context of the new geochemistry and age constraints of the WORMIL basalts. The new data reinforce previous interpretations that progressive rifting and transformation of the continental lithosphere to oceanic lithosphere allows for increasing asthenospheric inputs through time as the continental lithosphere is thinned. Accepted trace element values for BHVO-2 are those recently recommended by Jochum et al. (2016) rounded to provide the same significant figures as the data. Ternary model after Schilling et al. (1992); Endmembers from Rooney et al. (2012).

The evolution of complex type B Allende inclusion - An ion microprobe trace element study

NASA Technical Reports Server (NTRS)

Macpherson, Glenn J.; Crozaz, Ghislaine; Lundberg, Laura L.

1989-01-01

Results are presented of a detailed trace-element and isotopic analyses of the constituent phases in each of the major textural parts (mantle, core, and islands) of a Type B refractory inclusion, the USNM 5241 inclusion from Allende, first described by El Goresy et al. (1985). The REE data on 5241 were found to be largely consistent with a model in which the mantle and the core of 5241 formed sequentially out of a single melt by fractional crystallization. The numerical models of REE evolution in the 5241 melt, especially that of Eu, require that a significant mass of spinel-free island material was assimilated into the evolving melt during the last half of the solidification history of 5241. The trace element results pbtained thus strongly support the interpretation of El Goresy et al. (1985) that the spinel-free islands in the 5241 are trapped xenoliths.

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.

Major and trace element modeling of mid-ocean ridge mantle melting from the garnet to the plagioclase stability fields: Generating local and global compositional variability

NASA Astrophysics Data System (ADS)

Brown, S. M.; Behn, M. D.; Grove, T. L.

2017-12-01

We present results of a combined petrologic - geochemical (major and trace element) - geodynamical forward model for mantle melting and subsequent melt modification. The model advances Behn & Grove (2015), and is calibrated using experimental petrology. Our model allows for melting in the plagioclase, spinel, and garnet fields with a flexible retained melt fraction (from pure batch to pure fractional), tracks residual mantle composition, and includes melting with water, variable melt productivity, and mantle mode calculations. This approach is valuable for understanding oceanic crustal accretion, which involves mantle melting and melt modification by migration and aggregation. These igneous processes result in mid-ocean ridge basalts that vary in composition at the local (segment) and global scale. The important variables are geophysical and geochemical and include mantle composition, potential temperature, mantle flow, and spreading rate. Accordingly, our model allows us to systematically quantify the importance of each of these external variables. In addition to discriminating melt generation effects, we are able to discriminate the effects of different melt modification processes (inefficient pooling, melt-rock reaction, and fractional crystallization) in generating both local, segment-scale and global-scale compositional variability. We quantify the influence of a specific igneous process on the generation of oceanic crust as a function of variations in the external variables. We also find that it is unlikely that garnet lherzolite melting produces a signature in either major or trace element compositions formed from aggregated melts, because when melting does occur in the garnet field at high mantle temperature, it contributes a relatively small, uniform fraction (< 10%) of the pooled melt compositions at all spreading rates. Additionally, while increasing water content and/or temperature promote garnet melting, they also increase melt extent, pushing the pooled composition to lower Sm/Yb and higher Lu/Hf.

A relatively reduced Hadean continental crust

NASA Astrophysics Data System (ADS)

Yang, Xiaozhi; Gaillard, Fabrice; Scaillet, Bruno

2014-05-01

Among the physical and chemical parameters used to characterize the Earth, oxidation state, as reflected by its prevailing oxygen fugacity (fO2), is a particularly important one. It controls many physicochemical properties and geological processes of the Earth's different reservoirs, and affects the partitioning of elements between coexisting phases and the speciation of degassed volatiles in melts. In the past decades, numerous studies have been conducted to document the evolution of mantle and atmospheric oxidation state with time and in particular the possible transition from an early reduced state to the present oxidized conditions. So far, it has been established that the oxidation state of the uppermost mantle is within ±2 log units of the quartz-fayalite-magnetite (QFM) buffer, probably back to ~4.4 billion years ago (Ga) based on trace-elements studies of mantle-derived komatiites, kimberlites, basalts, volcanics and zircons, and that the O2 levels of atmosphere were initially low and rose markedly ~2.3 Ga known as the Great Oxidation Event (GOE), progressively reaching its present oxidation state of ~10 log units above QFM. In contrast, the secular evolution of oxidation state of the continental crust, an important boundary separating the underlying upper mantle from the surrounding atmosphere and buffering the exchanges and interactions between the Earth's interior and exterior, has rarely been addressed, although the presence of evolved crustal materials on the Earth can be traced back to ~4.4 Ga, e.g. by detrital zircons. Zircon is a common accessory mineral in nature, occurring in a wide variety of igneous, sedimentary and metamorphic rocks, and is almost ubiquitous in crustal rocks. The physical and chemical durability of zircons makes them widely used in geochemical studies in terms of trace-elements, isotopes, ages and melt/mineral inclusions; in particular, zircons are persistent under most crustal conditions and can survive many secondary processes such as metamorphism, weathering and erosion. Thus, zircons in granites of shallow crust may record the chemical/isotopic composition of the deep crust that is otherwise inaccessible, and offer robust records of the magmatic and crust-forming events preserved in the continental crust. In fact, due to the absence of suitable rock records (in particular for periods older than ~4.0 Ga), studies in recent years concerning the nature, composition, growth and evolution of the continental crust, and especially the Hadean crust, have heavily relied on inherited/detrital zircons. Natural igneous zircons incorporate rare-earth elements (REE) and other trace elements in their structure at concentrations controlled by the temperature, pressure, fO2 and composition of their crystallization environment. Petrological observations and recent experiments have shown that the concentration of Ce relative to other REE in igneous zircons can be used to constrain the fO2 during their growth. By combining available trace-elements data of igneous zircons of crustal origin, we show that the Hadean continental crust was significantly more reduced than its modern counterpart and experienced progressive oxidation till ~3.6 billions years ago. We suggest that the increase in the oxidation state of the Hadean continental crust is related to the progressive decline in the intensity of meteorite impacts during the late veneer. Impacts of carbon- and hydrogen-rich materials during the formation of Hadean granitic crust must have favoured strongly reduced magmatism. The conjunction of cold, wet and reduced granitic magmatism during the Hadean implies the degassing of methane and water. When impacts ended, magma produced by normal decompression melting of the mantle imparted more oxidizing conditions to erupted lavas and the related crust.

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.

Heterogeneous hydrogen distribution in orthopyroxene from veined mantle peridotite (San Carlos, Arizona): Impact of melt-rock interactions

NASA Astrophysics Data System (ADS)

Denis, Carole M. M.; Demouchy, Sylvie; Alard, Olivier

2018-03-01

Experimental studies have shown that hydrogen embedded as a trace element in mantle mineral structures affects the physical properties of mantle minerals and rocks. Nevertheless, hydrogen concentrations in mantle minerals are much lower than predicted by hydrogen solubilities obtained experimentally at high pressure and temperature. Here, we report textural analyses and major and trace element concentrations (including hydrogen) in upper mantle minerals from a spinel-bearing composite xenolith (dunite and pyroxenite) transported by silica-undersaturated mafic alkaline lavas from the San Carlos volcanic field (Arizona, USA). Our results suggest that the composite xenolith results from the percolation-reaction of a basaltic liquid within dunite channels, and is equilibrated with respect to trace elements. Equilibrium temperatures range between 1011 and 1023 °C. Hydrogen concentrations (expressed in ppm H2O by weight) obtained from unpolarized and polarized Fourier transform infrared spectroscopy are low, with average values <2 ppm H2O, 24 ppm H2O, and 53 ppm H2O for olivine, orthopyroxene, and clinopyroxene, respectively; hydrogen concentrations in olivine are below the detection limit. These low hydrogen concentrations are consistent with depletion by high melt-rock ratio interactions. Clinopyroxene hydrogen concentrations are homogeneous, whereas polarized infrared profile measurements across single-crystals of orthopyroxene reveal hydrogen-depleted rims, which are interpreted as the result of dehydration by ionic diffusion, possibly triggered by melt-rock interactions. We conclude that pyroxenes, like olivine, are unreliable hydrogen proxies, and that the remaining hydrogen concentrations observed in peridotites might only represent the 'tip of the iceberg' of the water stored in the Earth's upper mantle.

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.

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.

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.

Aqueous fluids and sedimentary melts as agents for mantle wedge metasomatism, as inferred from peridotite xenoliths at Pinatubo and Iraya volcanoes, Luzon arc, Philippines

NASA Astrophysics Data System (ADS)

Yoshikawa, Masako; Tamura, Akihiro; Arai, Shoji; Kawamoto, Tatsuhiko; Payot, Betchaida D.; Rivera, Danikko John; Bariso, Ericson B.; Mirabueno, Ma. Hannah T.; Okuno, Mitsuru; Kobayashi, Tetsuo

2016-10-01

Mantle xenoliths entrained in subduction-zone magmas often record metasomatic signature of the mantle wedge. Such xenoliths occur in magmas from Iraya and Pinatubo volcanoes, located at the volcanic front of the Luzon arc in the Philippines. In this study, we present the major element compositions of the main minerals, trace element abundances in pyroxenes and amphiboles, and Nd-Sr isotopic compositions of amphiboles in the peridotite xenoliths from Pinatubo volcano. The data indicate enrichment in fluid-mobile elements, such as Rb, Ba, U, Pb, and Sr, and Nd-Sr isotopic ratios relative to those of mantle. The results are considered in terms of mixing of asthenospheric mantle and subducting oceanic crustal components. The enrichments observed in the Pinatubo mantle xenoliths are much less pronounced than those reported for the Iraya mantle xenoliths. This disparity suggests differences in the metasomatic agents contributing to the two suites; i.e., aqueous fluids infiltrated the mantle wedge beneath the Pinatubo volcano, whereas aqueous fluids and sediment-derived melts infiltrated the mantle wedge beneath the Iraya volcano.

Petrogenesis of Late Cretaceous lava flows from a Ceno-Tethyan island arc: The Raskoh arc, Balochistan, Pakistan

NASA Astrophysics Data System (ADS)

Siddiqui, Rehanul Haq; Qasim Jan, M.; Asif Khan, M.

2012-10-01

The Raskoh arc is about 250 km long, 40 km wide and trends in an ENE direction. The oldest rock unit in the Raskoh arc is an accretionary complex (Early to Late Jurassic), which is followed in age by Kuchakki Volcanic Group, the most wide spread unit of the Raskoh arc. The Volcanic Group is mainly composed of basaltic to andesitic lava flows and volcaniclastics, including agglomerate, volcanic conglomerate, breccia and tuff, with subordinate shale, sandstone, limestone and chert. The flows generally form 3-15 m thick lenticular bodies but rarely reach up to 300 m. They are mainly basaltic-andesites with minor basalts and andesites. The main textures exhibited by these rocks are hypocrystalline porphyritic, subcumulophyric and intergranular. The phenocrysts comprise mainly plagioclase (An30-54 in Nok Chah and An56-64 in Bunap). They are embedded in a micro-cryptocrystalline groundmass having the same minerals. Apatite, magnetite, titanomagnetite and hematite occur as accessory minerals. Major, trace and rare earth elements suggest that the volcanics are oceanic island arc tholeiites. Their low Mg # (42-56) and higher FeO (total)/MgO (1.24-2.67) ratios indicate that the parent magma of these rocks was not directly derived from a mantle source but fractionated in an upper level magma chamber. The trace element patterns show enrichment in LILE and depletion in HFSE relative to N-MORB. Their primordial mantle-normalized trace element patterns show marked negative Nb anomalies with positive spikes on K, Ba and Sr which confirm their island arc signatures. Slightly depleted LREE to flat chondrite normalized REE patterns further support this interpretation. The Zr versus Zr/Y and Cr versus Y studies show that their parent magma was generated by 20-30% melting of a depleted mantle source. The trace elements ratios including Zr/Y (1.73-3.10), Ti/Zr (81.59-101.83), Ti/V (12.39-30.34), La/YbN (0.74-2.69), Ta/Yb (0.02-0.05) and Th/Yb (0.11-0.75) of the volcanics are more consistent with oceanic island arcs rather than continental margin arcs. It is suggested that the Raskoh arc is an oceanic island arc which formed due to the intra-oceanic convergence in the Ceno-Tethys during the Late Cretaceous rather than constructed on the southern continental margin of the Afghan block, as claimed by previous workers. It is further suggested that the Semail, Zagros, Chagai-Raskoh, Muslim Bagh, and Waziristan island arcs were developed in a single but segmented Cretaceous Ceno-Tethyan convergence zone.

Mesoproterozoic orangeites of Karelia (Kostomuksha-Lentiira): evidence for composition of mantle lithosphere

NASA Astrophysics Data System (ADS)

Kargin, Alexey; Nosova, Anna; Larionova, Yulia; Kononova, Voctoria; Borisovskiy, Sergey; Kovalchuk, Elena; Griboedova, Irina

2014-05-01

The 1.23-1.20 Ga old diamondiferous lamproites and orangeites (kimberlites of II group) of the Kostomuksha-Taloveys and the Lentiira-Kuhmo dyke fields intrude the Archaean crust of the Karelian craton, NE of the East European Platform. Mineral (a trend of compositional evolution of mica, presence of carbonate minerals in basis, composition of olivine) and geochemical (major elements, ratio of trace elements, primitive mantle normalized trace elements patterns) characteristics of these rocks suggest an orangeitic rather than lamproitic or lamprophyric nature. The composition of Phl-Ol orangeites suggests intensive processes of fractional crystallization for their melts. Cpx-Phl-Ol orangeites indicate higher intensity of lithospheric mantle assimilation then other orangeitic types. Phl-Carb orangeites of the Taloveys area and Cpx-Phl-Ol one of the Lentiira area are closest to primary melts. The Ol-Phl-Cpx orangeites of the Lentiira area contain three generations of unaltered olivine that vary in composition and origin: a) xenocryst derived from depleted mantle peridotite; b) orangeitic olivine phenocryst and c) and olivine like early stage crystallization of megacryst assemblage or a product of metasomatic interaction between mantle peridotite and protokimberlitic melt. Orangeites of Kostomuksha-Lentiira have low- and medium-radiogenic value of (87Sr/86Sr)1200 that range from 0.7038 to 0.7067. Phl-Carb orangeites of Taloveys have less radiogenic isotopic composition of Nd (eNd -11 ... -12) then Cpx-Phl-Ol and Phl-Ol orangeites of Kostomuksha (eNd -6.9 ... -9.4). The study of Sm-Nd and Rb-Sr isotopic systems suggests that an ancient metasomatic mantle source took part in origin of orangeites. We propose a two-steps model of origin of their source (Kargin et al., 2014): 1) The metasomatic component of mantle source (like as MARID-type veins) formed during Lapland-Kola and/or Svecofennian orogeny events (2.1-1.8 Ga ago). 2) The intrusion of orangeites is comparable by time and geological setting with back-arc extensions (such as magmatism of CSDG) during the first stage of Sveconorwegian orogeny, initial stage of assembly of the supercontinent Rodinia (1.31-1.14 Ga). These back-arc extensions inspired of asthenosphere-derived melts to metasomatic lithospheric mantle and a generation of orangeitic melts. Kargin A.V., Nosova A.A., Larionova Yu.O. et al. Mesoproterozoic orangeites (kimberlites II) of Western Karelia: mineralogical, geochemical and Nd-Sr isotopic-geochemical characteristics // Petrology. 2014. V.2. in press.

Water Contents of the Mantle Beneath the Rio Grande Rift: FTIR Analysis of Kilbourne Hole Peridotite Xenoliths

NASA Technical Reports Server (NTRS)

Schaffer, Lillian A.; Peslier, Anne; Brandon, Alan

2013-01-01

Although nominally anhydrous mantle minerals contain only trace amounts of water, they are the main reservoir of water in the mantle. Added up at the scale of the Earth's mantle, these trace amounts of water represent oceans worth in mass]. Mantle xenoliths from Kilbourne Hole in southern New Mexico are ideal to study mantle water distribution in a rift tectonic setting as they come from a recently-erupted maar in the middle of the Rio Grande Rift. Eleven lherzolites, one harzburgite, and one dunite are being analyzed for water contents by FTIR. The xenoliths will also be analyzed for major and trace element composition, Fe3+/Summation (Fe) ratios, and characterized petrologically. Olivines exhibit variable water contents with less water at the rims compared to the cores. This is probably due to H loss during decompression and xenolith transport by the host magma. Mantle water contents appear to have been primarily preserved in the core of the olivines, based on diffusion modeling of the typically plateau-shaped water content profiles across these grains. Water concentrations are in equilibrium between clino- and orthopyroxene, but olivine concentrations are typically not in equilibrium with those of either pyroxene. Lherzolites analyzed so far have water contents of 2-12 ppm H2O in olivines, 125-165 ppm H2O in orthopyroxenes, and 328-447 ppm H2O in clinopyroxenes. These water contents are similar to, but with a narrower range, than those for the respective minerals in other continental peridotite xenoliths. The lherzolites have bulk-rock (BR) Al2O3 contents that range between 3.17 and 3.78 wt%, indicating similar degrees of partial melting, which could explain the narrow range of their pyroxene water contents. Primitive mantle normalized rare earth element (REE) profiles of the bulk lherzolites vary from light REE depleted to flat, with no significant differences between, nor relation to, their mineral water contents. Consequently, the metasomatic agents that enriched LREEs in these lherzolites were most likely water-poor. The harzburgite and the dunite have lower weight percent Al2O3 compared to the lherzolites (2.11% and 0.34% respectively) indicating higher degrees of melting. Their olivine water contents, however, are similar to those of the lherzolites. Moreover, no correlations are observed between pyroxene water contents and indices of melting or metasomatism between the lherzolite group, the harzburgite, and the dunite, although the latter has the lowest pyroxene water contents. More samples will be analyzed to determine if the water contents are controlled by melting, metasomatism, or a combination of the two in the Kilbourne Hole mantle.

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.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Rapp, R.P.; Irifune, T.; Shimizu, N.

Isotopic and trace element geochemical studies of ocean island basalts (OIBs) have for many years been used to infer the presence of long-lived ({approx} 1-2 Ga old) compositional heterogeneities in the deep mantle related to recycling of crustal lithologies and marine and terrigenous sediments via subduction [e.g., Zindler, A., Hart, S.R., 1986. Chemical geodynamics. Annu. Rev. Earth Planet. Sci. 14, 493-571; Weaver, B.L., 1991. The origin of ocean island basalt end-member compositions: trace element and isotopic constraints. Earth Planet. Sci. Lett. 104, 381-397; Chauvel, C., Hofmann, A.W., Vidal, P., 1992. HIMU-EM: the French Polynesian connection. Earth Planet. Sci. Lett. 110,more » 99-119; Hofmann, A.W., 1997. Mantle geochemistry: the message from oceanic volcanism. Nature 385, 219-229; Willbold, M., Stracke, A., 2006. Trace element composition of mantle end-members: Implications for recycling of oceanic and upper and lower continental crust. Geochem. Geophys. Geosyst. Q04004. 7, doi:10.1029/2005GC001005]. In particular, models for the EM-1 type ('enriched mantle') OIB reservoir have invoked the presence of subducted, continental-derived sediment to explain high {sup 87}Sr/{sup 86}Sr ratios, low {sup 143}Nd/{sup 144}Nd and {sup 206}Pb/{sup 204}Pb ratios, and extreme enrichments in incompatible elements observed in OIB lavas from, for example, the Pitcairn Island group in the South Pacific [Woodhead, J.D., McCulloch, M.T., 1989; Woodhead, J.D., Devey, C.W., 1993. Geochemistry of the Pitcairn seamounts, I: source character and temporal trends. Earth Planet. Sci. Lett. 116, 81-99; Eisele, J., Sharma, M., Galer, S.J.G., Blichert-Toft, J., Devey, C.W., Hofmann, A.W., 2002. The role of sediment recycling in EM-1 inferred from Os, Pb, Hf, Nd, Sr isotope and trace element systematics of the Pitcairn hotspot. Earth Planet. Sci. Lett. 196, 197-212]. More recently, ultrapotassic, mantle-derived lavas (lamproites) from Gaussberg, Antarctica have been interpreted as the product of melting of deeply recycled (subducted) Archean-age metasediments in the mantle transition zone [Murphy, D.T., Collerson, K.D., Kamber, B.S., 2002. Lamproites from Gaussberg, Antartica: possible transition zone melts of Archaean subducted sediments. J. Petrol. 43, 981-1001]. Here we report the results of phase equilibria experiments on two different natural sedimentary compositions (a high-grade metapelite with < 1 wt.% H{sub 2}O, and a marine 'mud' with 8 wt.% H{sub O}) at 16-23 GPa. In both materials, the high-pressure mineral assemblages contain {approx} 15-30 wt.% K-hollandite (KAlSi{sub 3}O{sub 8}), in addition to stishovite, garnet, an Al-silicate phase (kyanite or phase egg), and a Fe-Ti spinel (corundum). Ion microprobe analyses of K-hollandite for a range of trace elements reveal that this phase controls a significant proportion of the whole-rock budget of incompatible, large-ion lithophile elements (LILEs, e.g., Rb, Ba, Sr, K, Pb, La, Ce and Th). Comparisons between the abundances and ratios of these elements in K-hollandite with those in EM-I type ocean-island basalts from Pitcairn Island and related seamounts, and with the Gaussberg lamproites, indicate the presence of deeply recycled, continent-derived sediments in these lavas sources. Our results suggest that the incompatible trace-element signature of EM-I OIB reservoirs in general and of the Gaussberg lamproites in particular can be attributed to recycling of K-hollandite-bearing continental sediments to transition zone depths.« less

Trace Element Accumulation and Tissue Distribution in the Purpleback Flying Squid Sthenoteuthis oualaniensis from the Central and Southern South China Sea.

PubMed

Wu, Yan Yan; Shen, Yu; Huang, Hui; Yang, Xian Qing; Zhao, Yong Qiang; Cen, Jian Wei; Qi, Bo

2017-01-01

Sthenoteuthis oualaniensis is a species of cephalopod that is becoming economically important in the South China Sea. As, Cd, Cr, Cu, Hg, Pb, and Zn concentrations were determined in the mantle, arms, and digestive gland of S. oualaniensis from 31 oceanographic survey stations in the central and southern South China Sea. Intraspecific and interspecific comparisons with previous studies were made. Mean concentrations of trace elements analyzed in arms and mantle were in the following orders: Zn > Cu > Cd > Cr > As > Hg. In digestive gland, the concentrations of Cd and Cu exceed that of Zn. All the Pb concentrations were under the detected limit.

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.

Petrogenesis of early Jurassic basalts in southern Jiangxi Province, South China: Implications for the thermal state of the Mesozoic mantle beneath South China

NASA Astrophysics Data System (ADS)

Cen, Tao; Li, Wu-xian; Wang, Xuan-ce; Pang, Chong-jin; Li, Zheng-xiang; Xing, Guang-fu; Zhao, Xi-lin; Tao, Jihua

2016-07-01

Early Jurassic bimodal volcanic and intrusive rocks in southern South China show distinct associations and distribution patterns in comparison with those of the Middle Jurassic and Cretaceous rocks in the area. It is widely accepted that these rocks formed in an extensional setting, although the timing of the onset and the tectonic driver for extension are debated. Here, we present systematic LA-ICP-MS zircon U-Pb ages, whole-rock geochemistry and Sr-Nd isotope data for bimodal volcanic rocks from the Changpu Formation in the Changpu-Baimianshi and Dongkeng-Linjiang basins in southern Jiangxi Province, South China. Zircon U-Pb ages indicate that the bimodal volcanic rocks erupted at ca. 190 Ma, contemporaneous with the Fankeng basalts ( 183 Ma). A compilation of geochronological results demonstrates that basin-scale basaltic eruptions occurred during the Early Jurassic within a relatively short interval (< 5 Ma). These Early Jurassic basalts have tholeiitic compositions and OIB-like trace element distribution patterns. Geochemical analyses show that the basalts were derived from depleted asthenospheric mantle, dominated by a volatile-free peridotite source. The calculated primary melt compositions suggest that the basalts formed at 1.9-2.1 GPa, with melting temperatures of 1378 °C-1405 °C and a mantle potential temperature (TP) ranging from 1383 °C to 1407 °C. The temperature range is somewhat hotter than normal mid-ocean-basalt (MORB) mantle but similar to an intra-plate continental mantle setting, such as the Basin and Range Province in western North America. This study provides an important constraint on the Early Jurassic mantle thermal state beneath South China. Reference: Raczek, I., Stoll, B., Hofmann, A.W., Jochum, K.P. 2001. High-precision trace element data for the USGS reference materials BCR-1, BCR-2, BHVO-1, BHVO-2, AGV-1, AGV-2, DTS-1, DTS-2, GSP-1 and GSP-2 by ID-TIMS and MIC-SSMS. Geostandards Newsletter 25(1), 77-86.

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.

Trace elements in olivine of ultramafic lamprophyres controlled by phlogopite-rich mineral assemblages in the mantle source

NASA Astrophysics Data System (ADS)

Veter, Marina; Foley, Stephen F.; Mertz-Kraus, Regina; Groschopf, Nora

2017-11-01

Carbonate-rich ultramafic lamprophyres (aillikites) and associated rocks characteristically occur during the early stages of thinning and rifting of cratonic mantle lithosphere, prior to the eruption of melilitites, nephelinites and alkali basalts. It is accepted that they require volatile-rich melting conditions, and the presence of phlogopite and carbonate in the source, but the exact source rock assemblages are debated. Melts similar to carbonate-rich ultramafic lamprophyres (aillikites) have been produced by melting of peridotites in the presence of CO2 and H2O, whereas isotopes and trace elements appear to favor distinct phlogopite-bearing rocks. Olivine macrocrysts in aillikites are usually rounded and abraded, so that it is debated whether they are phenocrysts or mantle xenocrysts. We have analyzed minor and trace element composition in olivines from the type aillikites from Aillik Bay in Labrador, Canada. We characterize five groups of olivines: [1] mantle xenocrysts, [2] the main phenocryst population, and [3] reversely zoned crystals interpreted as phenocrysts from earlier, more fractionated, magma batches, [4] rims on the phenocrysts, which delineate aillikite melt fractionation trends, and [5] rims around the reversely zoned olivines. The main phenocryst population is characterized by mantle-like Ni (averaging 3400 μg g- 1) and Ni/Mg at Mg# of 88-90, overlapping with phenocrysts in ocean island basalts and Mediterranean lamproites. However, they also have low 100 Mn/Fe of 0.9-1.3 and no correlation between Ni and other trace elements (Sc, Co, Li) that would indicate recycled oceanic or continental crust in their sources. The low Mn/Fe without high Ni/Mg, and the high V/Sc (2-5) are inherited from phlogopite in the source that originated by solidification of lamproitic melts at the base of the cratonic lithosphere in a previous stage of igneous activity. The olivine phenocryst compositions are interpreted to result from phlogopite and not high modal pyroxene in the source. The presence of kimberlites and ultramafic lamprophyres of Mesozoic age in Greenland indicates the persistence of a steep edge to the cratonic lithosphere at a time when this had been removed from the western flank in Labrador.

Olivine-hosted melt inclusions record efficient mixing of mantle melts in continental flood basalt provinces

NASA Astrophysics Data System (ADS)

Jennings, E. S.; Gibson, S. A.; Maclennan, J.; Heinonen, J. S.

2017-12-01

Primitive melt inclusions trapped in various minerals found in global ridge settings have been shown to record highly variable magmatic compositions. Mantle melting is expected to be near-fractional, producing a wide range of melt compositions that must accumulate and mix in crustal magma chambers. In primitive rocks, the melt inclusion variability observed in major, trace and isotope geochemistry is consistent to the first order with partial melting of variably depleted mantle, and indicate that the host phases began to crystallise prior to the completion of melt aggregation and mixing. We present new major and trace element data from a large number of rehomogenised olivine-hosted melt inclusions from the Cretaceous Paraná-Etendeka and Jurassic Karoo continental flood basalt (CFB) provinces [1]. We show that the major element chemistry of the melt inclusions can be severely disrupted by the rehomogenisation process and, as a consequence, their initial compositions cannot easily be back-calculated. However, despite the age of the samples, the trace element geochemistry of the melt inclusions is well-preserved. Despite coming from near-liquidus olivines from primitive picrites and ferropicrites, the inclusions are remarkably homogeneous; none of the anticipated variability in incompatible trace element compositions is observed. When considered alongside literature data, it appears that variability in primitive melts - as recorded by melt inclusions - is low in CFBs and OIBs relative to ridge settings, e.g. Iceland. We suggest that the tectonic setting imposes a control on the mixing of mantle melts: hot, plume-derived melts generated beneath relatively thick lithosphere may be prone to efficient mixing, perhaps due to their low viscosity, long transport pathways, and/or a superliquidus emplacement temperature [1]. This interpretation is supported by the almost non-existent variability of olivine-hosted inclusions from ferropicrite samples: these magmas represents the deepest, hottest and lowest viscosity magma of all the samples considered. [1] Jennings E. S., Gibson S. A., Maclennan J. and Heinonen J. S. (2017) Deep mixing of mantle melts beneath continental flood basalt provinces: Constraints from olivine-hosted melt inclusions in primitive magmas. Geochimica et Cosmochimica Acta 196, 36-57.

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.

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.

Olivine inclusions in Siberian diamonds and mantle xenoliths: Contrasting water and trace-element contents

NASA Astrophysics Data System (ADS)

Jean, M. M.; Taylor, L. A.; Howarth, G. H.; Peslier, A. H.; Fedele, L.; Bodnar, R. J.; Guan, Y.; Doucet, L. S.; Ionov, D. A.; Logvinova, A. M.; Golovin, A. V.; Sobolev, N. V.

2016-11-01

A subject of continuing debate is how the Earth's lithospheric portion of the upper mantle has remained the thickest (> 200 km) and oldest (> 3 Gy) beneath cratons and is yet surrounded by a vigorously convecting asthenosphere. It is generally admitted that water is a key parameter in the strength and longevity of cratonic roots, because olivine, the main phase of the lithospheric mantle, becomes stronger if its water content decreases. Expanding upon the work presented in Novella et al. (2015) and Taylor et al. (2016), we report new water contents for additional olivine inclusions in diamonds together with the trace-element composition for all olivine inclusions, as well as for mantle xenoliths from various kimberlite pipes located on the Siberian craton. The olivine diamond inclusions from this study have systematically low-water contents (< 50 ppmw H2O), moderate to high forsterite (e.g., Fo91-94) contents and low Ni, Co, and Zn ppm contents (e.g., < 2848, < 108, and < 47 ppm, respectively). In contrast, olivines from Siberian craton mantle xenoliths have a wide range of water contents (6-323 ppmw H2O) and extend to lower-Fo (91-92), Ni, Co, and Zn-rich compositions, compared to the diamond inclusions. Depleted incompatible trace-element concentrations in olivine (0.1-0.001 × Primitive Mantle) advance our hypothesis for the protogenetic origins for the majority of Siberian diamond inclusions. These observations are consistent with the peridotite xenoliths as representing a part of the cratonic lithosphere that has experienced melt re-fertilization, which has also transported water. The olivine diamond inclusions, on the other hand, preserve "micro-samples" of an initial, dry cratonic lithosphere, mostly resulting from melting events. These inclusions are likely sourced from the initial cratonic mantle lithosphere, which thereby, resisted delamination over time, due to its buoyancy and strength, imparted from melt and water depletion, respectively. And thus, our data provides a major argument that the kimberlite-hosted mantle xenoliths may be more metasomatized than common rocks at the base of the Siberian and other cratonic roots away from kimberlite fields.

Trace Elements in Basalts From the Siqueiros Fracture Zone: Implications for Melt Migration Models

NASA Astrophysics Data System (ADS)

Pickle, R. C.; Forsyth, D. W.; Saal, A. E.; Nagle, A. N.; Perfit, M. R.

2008-12-01

Incompatible trace element (ITE) ratios in MORB from a variety of locations may provide insights into the melt migration process by constraining aggregated melt compositions predicted by mantle melting and flow models. By using actual plate geometries to create a 3-D thermodynamic mantle model, melt volumes and compositions at all depths and locations may be calculated and binned into cubes using the pHMELTS algorithm [Asimow et al., 2004]. These melts can be traced from each cube to the surface assuming several migration models, including a simplified pressure gradient model and one in which melt is guided upwards by a low permeability compacted layer. The ITE ratios of all melts arriving at the surface are summed, averaged, and compared to those of the actual sample compositions from the various MOR locales. The Siqueiros fracture zone at 8° 20' N on the East Pacific Rise (EPR) comprises 4 intra-transform spreading centers (ITSCs) across 140 km of offset between two longer spreading ridges, and is an excellent study region for several reasons. First, an abundance of MORB data is readily available, and the samples retrieved from ITSCs are unlikely to be aggregated in a long-lived magma chamber or affected by along-axis transport, so they represent melts extracted locally from the mantle. Additionally, samples at Siqueiros span a compositional range from depleted to normal MORB within the fracture zone yet have similar isotopic compositions to samples collected from the 9-10° EPR. This minimizes the effect of assuming a uniform source composition in our melting model despite a heterogeneous mantle, allowing us to consistently compare the actual lava composition with that predicted by our model. Finally, it has been demonstrated with preliminary migration models that incipient melts generated directly below an ITSC may not necessarily erupt at that ITSC but migrate laterally towards a nearby ridge due to enhanced pressure gradients. The close proximity of the ITSCs at Siqueiros to the large ridges bounding the fracture zone provide a good opportunity to model this phenomenon and may help explain the variable ITE ratios found between samples collected within the transform and those near the ridges.

Melting mode and source lithology inferred from trace element systematic in historical olivine from Lanzarote, Canary Islands

NASA Astrophysics Data System (ADS)

Gómez-Ulla, Alejandra; Sigmarsson, Olgeir; Guðfinnsson, Guðmundur H.

2017-04-01

Trace element concentrations and ratios in olivine phenocrysts, such as fractionation-corrected Ni x (FeO/MgO) and Fe/Mn, have been shown useful as probes of pyroxenite derived component in mixtures of primary mantle melts (e.g. Sobolev et al., 2007). For instance, higher Ni and lower Mn and Ca contents are expected in partial melts of pyroxenite compared to those of lherzolite. We have measured trace element concentrations in olivine from 1730-1736 AD (Timanfaya) and 1824 AD eruptions in Lanzarote (Canary Islands), which erupted mafic and mantle nodule bearing magmas, ranging in composition from highly silica-undersaturated basanite through alkali basalt to tholeiite. The early basanite exhibit the largest olivine trace element variation covering the range of those from MORB and OIB worldwide, whereas later erupted tholeiite have values typical from pyroxenite derived melts. The Fo value decreased systematically with time during the 1730-36 eruption and the proportion of silica-saturated primary melt increased in the parental magma mixture with time. At the end of the eruption, tholeiite magmas crystallized olivine with, increasing concentrations of Mn and Ca and higher Ca/Al at relatively uniform Ni x (FeO/MgO) and Fe/Mn, all of which is readily explained by increased decompression melting at lower temperature. The basanite from the eruption that took place in 1824 AD has olivine with even higher Fo value and trace element variability similar those of the Timanfaya basanite. The fact that the Lanzarote basanite contain olivine with trace element systematic spanning that of MORB and pyroxenite melt can be explained by CO2-flux melting of a lithologically heterogeneous source, generating the diverse compositions. Initial reactive porous flow through depleted oceanic lithosphere and equilibration with dunitic restite of percolating pyroxenite melt may have amplified the observed Ni depletion in olivine of the earliest basanite. The fact that olivine compositions and basanite magma were reproduced approximately a century later may reflect episodic carbonatic fluxing in the slowly uprising Canarian mantle plume.

Isotopic evolution of Mauna Loa Volcano: A view from the submarine southwest rift zone

NASA Astrophysics Data System (ADS)

Kurz, Mark D.; Kenna, T. C.; Kammer, D. P.; Rhodes, J. Michael; Garcia, Michael O.

New isotopic and trace element measurements on lavas from the submarine southwest rift zone (SWR) of Mauna Loa continue the temporal trends of subaerial Mauna Loa flows, extending the known compositional range for this volcano, and suggesting that many of the SWR lavas are older than any exposed on land. He and Nd isotopic compositions are similar to those in the oldest subaerial Mauna Loa lavas (Kahuku and Ninole Basalts), while 87Sr/86Sr ratios are slightly lower (as low as .7036) and Pb isotopes are higher (206Pb'204Pb up to 18.30). The coherence of all the isotopes suggests that helium behaves as an incompatible element, and that helium isotopic variations in the Hawaiian lavas are produced by melting and mantle processes, rather than magma chamber or metasomatic processes unique to the gaseous elements. The variations of He, Sr, and Nd are most pronounced in lavas of approximately 10 ka age range [Kurz and Kammer, 1991], but the largest Pb isotopic variation occurs earlier. These variations are interpreted as resulting from the diminishing contribution from the upwelling mantle plume material as the shield building ends at Mauna Loa. The order of reduction in the plume isotopic signature is inferred to be Pb (at >100 ka), He (at ˜14 ka), Sr (at ˜9 ka), and Nd (at ˜8 ka); the different timing may relate to silicate/melt partition coefficients, with most incompatible elements removed first, and also to concentration variations within the plume. Zr/Nb, Sr/Nb, and fractionation-corrected Nb concentrations, correlate with the isotopes and are significantly higher in some of the submarine SWR lavas, suggesting temporal variability on time scales similar to the Pb isotopes (i.e. ˜ 100 ka). Historical lavas define trace element and isotopic trends that are distinct from the longer term (10 to 100 ka) variations, suggesting that different processes cause the short term variability. The temporal evolution of Mauna Loa, and particularly the new data from the submarine SWR, suggest that the isotopic composition of the upwelling plume mantle is best represented by data from Loihi seamount tholeiites. The temporal evolution suggests that the mantle source of the latest stage of Mauna Loa, which is characterized by radiogenic 87Sr/86Sr (up to .70395), unradiogenic 206Pb/204Pb (˜18.0), 3He/4He ratios similar to MORB, and low Nb concentrations, is a small-volume contribution related to non-plume components (such as normal asthenosphere, or entrained mantle).

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.

Major and trace element, and Sr isotope compositions of clinopyroxene phenocrysts in mafic dykes on Jiaodong Peninsula, southeastern North China Craton: Insights into magma mixing and source metasomatism

NASA Astrophysics Data System (ADS)

Liang, Yayun; Deng, Jun; Liu, Xuefei; Wang, Qingfei; Qin, Cheng; Li, Yan; Yang, Yi; Zhou, Mian; Jiang, Jieyan

2018-03-01

Early Cretaceous mafic dyke swarms are widely developed on Jiaodong Peninsula in the southeastern part of the North China Craton (NCC), but their petrogenesis remains enigmatic. We have examined the in-situ major element, trace element and Sr isotope compositions of the clinopyroxene phenocrysts in these dykes in order to evaluate the extent of magma mixing and source metasomatism. Depending on the type of mineral zoning, the clinopyroxene phenocrysts in our samples can be classified into two groups: Group I (reverse zoning) and Group II (no zoning). Based on core compositions, the Group I phenocrysts with obvious reverse zoning can be divided into two subgroups: Groups IA and IB. The cores of Group IA clinopyroxenes have low values of Mg#, low Al2O3 contents, high Na2O contents, and high 87Sr/86Sr ratios, and they were probably derived from newly accreted lower crust that formed through the underplating of basaltic magma. In contrast, the cores of Group IB clinopyroxenes have lower Mg# values and lower contents of Al2O3, ΣREE (total rare earth elements), and incompatible elements, but they have similar 87Sr/86Sr ratios; these cores crystallised from crust-derived andesitic-dacitic magma. Group IA and IB clinopyroxene phenocryst rims (Group I rims) all have similar compositions with higher values of Mg# and higher Al2O3, Cr and Ni contents than the cores. The rims have high 87Sr/86Sr ratios, are enriched in LREEs (light rare earth elements) and LILEs (large ion lithophile elements), and are depleted in HFSEs (high field strength elements); these characteristics indicate that all the high-Mg rims were derived from a similar magma, possibly a relatively primitive magma derived from lithospheric mantle. We suggest, therefore, that the reversely-zoned clinopyroxene phenocrysts (Group I) in the Jiaodong mafic dykes provide evidence of magma mixing between a magma derived from lithospheric mantle and crust-derived andesitic-dacitic melt alongside with the newly accreted lower crust. The Group II clinopyroxene phenocrysts, which lack zoning, display major and trace element compositions and 87Sr/86Sr ratios that are similar to those of the Group I rims, which indicates that all the high-Mg clinopyroxenes were derived from a common source in the lithospheric mantle. These high-Mg clinopyroxenes exhibit high 87Sr/86Sr ratios, high Sr contents and remarkable depletions in HFSEs, reflecting metasomatism of the mantle source by aqueous fluids derived by dehydration of the subducting slab and its marine sediments. The metasomatism of the source reveals that the lithospheric mantle beneath Jiaodong Peninsula was metasomatised by fluids from the subducting Paleo-Pacific slab. Progressive thinning of the lithosphere mantle under the NCC was induced by continuous thermo-mechanical erosion, promoting the partial melting of lithospheric mantle and generating the mafic dykes at Jiaodong. Table A2 Analytical results for the trace element standards used during LA-ICP-MS analyses of clinopyroxene phenocrysts. Table A3 Analytical results for the Sr isotope standards used during MC-ICP-MS analyses of clinopyroxene phenocrysts. Table A4 Major element contents (wt%) of clinopyroxene phenocrysts from the mafic dykes on Jiaodong Peninsula. Table A5 Representative Sr isotopic compositions of clinopyroxene phenocrysts from the mafic dykes on Jiaodong Peninsula. Table A6 Geochemistry of the mafic dykes on Jiaodong Peninsula. Table A7 Partition coefficients (KD) and end-member components used for REE modeling.

Majorite-Garnet Partitioning of the Highly Siderophile Elements: New Results and Application to Mars

NASA Technical Reports Server (NTRS)

Danielson, L. R.; Righter, K.; Waeselmann, N.; Humayun, M.

2015-01-01

HSE and Os isotopes are used to constrain processes such as accretion, mantle evolution, crustal recycling, and core-mantle mixing, and to constrain the timing and depth of differentiation of Mars. Although showed that the HSE contents of the martian mantle could have been established by metal-silicate equilibrium in early Mars, the role of a cooling magma ocean and associated crystallization in further fractionating the HSEs is unclear. Garnet is thought to have played an important role in controlling trace element concentrations in the martian mantle reservoirs. However, testing these models, including Os isotopes, has been hindered by a dearth of partitioning data for the HSE in deep mantle phases - majorite, wadsleyite, ringwoodite, akimotoite - that may be present in the martian mantle. We examine the partitioning behavior of HSEs between majorite garnet (gt), olivine (oliv), and silicate liquid (melt).

Chemical interactions in the subduction factory: New insights from an in situ trace element and hydrogen study of the Ichinomegata and Oki-Dogo mantle xenoliths (Japan)

NASA Astrophysics Data System (ADS)

Satsukawa, Takako; Godard, Marguerite; Demouchy, Sylvie; Michibayashi, Katsuyoshi; Ildefonse, Benoit

2017-07-01

The uppermost mantle in back arc regions is the site of complex interactions between partial melting, melt percolation, and fluid migration. To constrain these interactions and evaluate their consequences on geochemical cycles, we carried out an in situ trace element and water study of a suite of spinel peridotite xenoliths from two regions of the Japan back arc system, Ichinomegata (NE Japan) and Oki-Dogo (SW Japan), using LA-ICPMS and FTIR spectrometry, respectively. This study provides the first full dataset of trace element and hydrogen compositions in peridotites including analyses of all their main constitutive silicate minerals: olivine, orthopyroxene and clinopyroxene. The Ichinomegata peridotites sample a LREE-depleted refractory mantle (Mg# olivine = 0.90; Cr# spinel = 0.07-0.23; Yb clinopyroxene = 7.8-13.3 × C1-chondrite, and La/Yb clinopyroxene = 0.003-0.086 × C1-chondrite), characterized by Th-U positive anomalies and constant values of Nb/Ta. The composition of the studied Ichinomegata samples is consistent with that of an oceanic mantle lithosphere affected by cryptic metasomatic interactions with hydrous/aqueous fluids (crypto-hydrous metasomatism). In contrast, the Oki-Dogo peridotites have low Mg# olivine (0.86-0.93) and a broad range of compositions with clinopyroxene showing "spoon-shaped" to flat, and LREE-enriched patterns. They are also characterized by their homogeneous compositions in the most incompatible LILE (e.g., Rb clinopyroxene = 0.01-0.05 × primitive mantle) and HFSE (e.g., Nb clinopyroxene = 0.01-2.16 × primitive mantle). This characteristic is interpreted as resulting from various degrees of melting and extensive melt-rock interactions. FTIR spectroscopy shows that olivine in both Ichinomegata and Oki-Dogo samples has low water contents ranging from 2 to 7 ppm wt. H2O. In contrast, the water contents of pyroxenes from Ichinomegata peridotites (113-271 ppm wt. H2O for orthopyroxene, and 292-347 ppm wt. H2O for clinopyroxene) are significantly higher than in Oki-Dogo peridotites (9-35 ppm wt. H2O for orthopyroxene, and 15-98 ppm wt. H2O for clinopyroxene). This indicates a relationship between melt-rock interaction and water concentrations in pyroxenes. Our study suggests that the water content of the Japan mantle wedge is controlled by the late melt/fluid/rock interactions evidenced by trace element geochemistry: a mechanism triggered by magma-rock interactions may have acted as an efficient dehydrating process in the Oki-Dogo region while the Ichinomegata mantle water content is controlled by slab-derived crypto-hydrous metasomatism.

Key new pieces of the HIMU puzzle from olivines and diamond inclusions.

PubMed

Weiss, Yaakov; Class, Cornelia; Goldstein, Steven L; Hanyu, Takeshi

2016-09-29

Mantle melting, which leads to the formation of oceanic and continental crust, together with crust recycling through plate tectonics, are the primary processes that drive the chemical differentiation of the silicate Earth. The present-day mantle, as sampled by oceanic basalts, shows large chemical and isotopic variability bounded by a few end-member compositions. Among these, the HIMU end-member (having a high U/Pb ratio, μ) has been generally considered to represent subducted/recycled basaltic oceanic crust. However, this concept has been challenged by recent studies of the mantle source of HIMU magmas. For example, analyses of olivine phenocrysts in HIMU lavas indicate derivation from the partial melting of peridotite, rather than from the pyroxenitic remnants of recycled oceanic basalt. Here we report data that elucidate the source of these lavas: high-precision trace-element analyses of olivine phenocrysts point to peridotite that has been metasomatized by carbonatite fluids. Moreover, similarities in the trace-element patterns of carbonatitic melt inclusions in diamonds and HIMU lavas indicate that the metasomatism occurred in the subcontinental lithospheric mantle, fused to the base of the continental crust and isolated from mantle convection. Taking into account evidence from sulfur isotope data for Archean to early Proterozoic surface material in the deep HIMU mantle source, a multi-stage evolution is revealed for the HIMU end-member, spanning more than half of Earth's history. Before entrainment in the convecting mantle, storage in a boundary layer, upwelling as a mantle plume and partial melting to become ocean island basalt, the HIMU source formed as Archean-early Proterozoic subduction-related carbonatite-metasomatized subcontinental lithospheric mantle.

In-situ trace element and Sr isotopic compositions of mantle xenoliths constrain two-stage metasomatism beneath the northern North China Craton

NASA Astrophysics Data System (ADS)

Wu, Dan; Liu, Yongsheng; Chen, Chunfei; Xu, Rong; Ducea, Mihai N.; Hu, Zhaochu; Zong, Keqing

2017-09-01

Subduction and collision are the key processes triggering geochemical refertilization of the lithospheric mantle beneath cratons. However, the way that the subducted plate influences the cratonic lithospheric mantle remains unclear. Here, in-situ major and trace-element and Sr isotopic compositions of peridotite and pyroxenite xenoliths carried by the Dongbahao Cenozoic basalts, located close to the northern margin of North China Craton (NCC), were examined to investigate the effects of the subducted Paleo-Asian oceanic plate on the lithospheric mantle of the NCC. Based on petrographic and geochemical features, peridotites were subdivided into two types recording two-stage metasomatism. Clinopyroxene (Cpx) in both types of peridotites show chemical zoning. In those peridotites we refer to as Type 1 peridotites, Cpx exhibit uniform convex-upward rare earth element (REE) patterns but core-rim variations in 87Sr/86Sr ratios (0.7065-0.7082 in the cores and 0.7043-0.7059 in the spongy rims), and have high (La/Yb)N ratios (> 1.12) (N means normalized to chondrite), relatively low Ti/Eu ratios (< 3756) and negative high field strength element (HFSE) (Nb, Ta, Zr, Hf and Ti) anomalies in the cores, indicating early-stage metasomatism by carbonatitic melts derived from the subducted sedimentary carbonate rocks. Cpx in the Type 2 peridotites have highly variable REE patterns (from light rare earth element (LREE)-depleted to LREE-enriched) and feature zoned Sr isotopic compositions contrasting to those in Type 1, i.e., increasing 87Sr/86Sr ratios from the cores (0.7020-0.7031) to the spongy rims (0.7035-0.7041). Accompanying variations of 87Sr/86Sr ratios, Cpx in both types of peridotites display increasing Nb/La ratios from the cores to the spongy rims. In addition, Cpx in the Type 2 peridotites show remarkably increased (La/Yb)N, Ca/Al, Sm/Hf and Zr/Hf ratios but decreased Ti/Eu and Ti/Nb ratios from the cores to the spongy rims. These features imply a later-stage metasomatism by CO2-rich silicate melts derived from carbonated eclogites. Pyroxenites were also classified into two types. Both types of pyroxenites show higher Ni content in Cpx and orthopyroxene than peridotites at the same Mg# (= 100 ∗ Mg/(Mg + Fe), atomic number) level. Their Cpx show high Ti/Eu, Ti/Sr ratios and similar 87Sr/86Sr ratios (0.7039-0.7055) to the Cpx spongy rims in peridotites, suggesting that pyroxenites originated from silicate melt-peridotite reactions in the later-stage metasomatism. These observations collectively indicate that the lithospheric mantle beneath the northern NCC presents evidence for two distinct mantle metasomatic events. We propose that both were caused by the subduction of the Paleo-Asian oceanic plate, which could have contributed significantly to the transformation of the lithospheric mantle beneath the northern NCC.

Albanian ophiolites as probes of a mantle heterogeneity study

NASA Astrophysics Data System (ADS)

Meisel, Thomas; Ginley, Stephen; Koller, Friedrich; Walker, Richard J.

2013-04-01

Most ophiolites are believed to be tectonically obducted slivers of oceanic lithosphere. As such they can provide information not only about the history of crust formation, but also about the composition of the chemical composition of the recent and ancient mantle composition. The occurrence of the well preserved Albanian Ophiolite Complex covers the length of Albania (ca. 150 km) is an ideal object not only for the study of the history of Jurassic tectonic event, but also for the study of the heterogeneity of the upper oceanic mantle from a millimeter to a 100 km scale. The occurrence of two almost parallel ophiolite chains, which have been described to be of different petrography presenting different parts of the upper mantle (MOR vs. SSZ type), allows the investigation of additional aspects of mantle heterogeneity. In this study we want to take advantage of the geochemical characteristics of platinum group elements (PGE) and of lithophile elements to estimate the extant of mantle melting, metasomatic and mixing events of a large portion of mantle obducted contemporaneously. In a first step only peridotites from the mantle sections of the ophiolite complexes are studied for the PGE content and the osmium isotopic composition. Together with major and trace element compositional data, following tasks will be addressed: development of a strategy for field and lab sampling, identification of processes that happened before and after obduction such as melt depletion, metasomatism, serpentinisation etc. and the determination of the size of modified and "pristine" domains. Samples from the western Albanian Ophiolite belt have been studied so far. Although the locations spread over the entire belt a remarkable similarity of PGE abundances is observed. In detail deviations from a correlation of Lu and TiO2 concentration data are also reflected in aberrant mantle normalized PGE patterns. Interestingly enough, this behavior is not manifested in a trend in the 187Os/188Os distribution. As a result the Os isotopic compositions of the entire belt represent the range to be expected from a post Archean upper mantle. The observed heterogeneous distribution of osmium isotopic compositions is most likely an image of the long depletion and incomplete remixing history of the upper Earth's mantle which was not significantly modified through event leading to the formation of ophiolite belts.

Continental basalts record the crust-mantle interaction in oceanic subduction channel: A geochemical case study from eastern China

NASA Astrophysics Data System (ADS)

Xu, Zheng; Zheng, Yong-Fei

2017-09-01

Continental basalts, erupted in either flood or rift mode, usually show oceanic island basalts (OIB)-like geochemical compositions. Although their depletion in Sr-Nd isotope compositions is normally ascribed to contributions from the asthenospheric mantle, their enrichment in large ion lithophile elements (LILE) and light rare earth elements (LREE) is generally associated with variable enrichments in the Sr-Nd isotope compositions. This indicates significant contributions from crustal components such as igneous oceanic crust, lower continental crust and seafloor sediment. Nevertheless, these crustal components were not incorporated into the mantle sources of continental basalts in the form of solidus rocks. Instead they were processed into metasomatic agents through low-degree partial melting in order to have the geochemical fractionation of the largest extent to achieve the enrichment of LILE and LREE in the metasomatic agents. Therefore, the mantle sources of continental basalts were generated by metasomatic reaction of the depleted mid-ocean ridge basalts (MORB) mantle with hydrous felsic melts. Nevertheless, mass balance considerations indicate differential contributions from the mantle and crustal components to the basalts. While the depleted MORB mantle predominates the budget of major elements, the crustal components predominate the budget of melt-mobile incompatible trace elements and their pertinent radiogenic isotopes. These considerations are verified by model calculations that are composed of four steps in an ancient oceanic subduction channel: (1) dehydration of the subducting crustal rocks at subarc depths, (2) anataxis of the dehydrated rocks at postarc depths, (3) metasomatic reaction of the depleted MORB mantle peridotite with the felsic melts to generate ultramafic metasomatites in the lower part of the mantle wedge, and (4) partial melting of the metasomatites for basaltic magmatism. The composition of metasomatites is quantitatively dictated by the crustal metasomatism through melt-peridotite reaction at the slab-mantle interface in oceanic subduction channels. Continental basalts of Mesozoic to Cenozoic ages from eastern China are used as a case example to illustrate the above petrogenetic mechanism. Subduction of the paleo-Pacific oceanic slab beneath the eastern edge of Eurasian continent in the Early Mesozoic would have transferred the crustal signatures into the mantle sources of these basalts. This process would be associated with rollback of the subducting slab at that time, whereas the partial melting of metasomatites takes place mainly in the Late Mesozoic to Cenozoic to produce the continental basalts. Therefore, OIB-like continental basalts are also the product of subduction-zone magmatism though they occur in intraplate settings.

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.

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 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.

Trace element concentrations in the top predator jumbo squid (Dosidicus gigas) from the Gulf of California.

PubMed

Raimundo, Joana; Vale, Carlos; Rosa, Rui

2014-04-01

Jumbo (or Humboldt) squid, Dosidicus gigas, is a large jet-propelled top oceanic predator off the Eastern Pacific. The present study reports, for the first time, concentrations of V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Cd and Pb in gills, mantle and digestive gland of this powerful pelagic squid in the Gulf of California. Zinc and Cu were the most abundant elements. All elements, with the exception of As, were largely stored in digestive gland; particularly Cd that reached concentrations between 57 and 509 µg g(-1). Significant relationships between tissues were found for Co (digestive gland-gills), As (gills-mantle) and Cd (digestive gland-mantle). Proportionality of Cd concentrations between mantle and digestive gland suggested that detoxification capacity by digestive gland was insufficient to avoid the transfer of this element to mantle and other tissues. Nonetheless, Cd concentrations in the mantle were always below the regulatory limit and, therefore lack of constraints for human consumption. On the basis of the fishery landings, one may estimate that up to 1t of Cd can be annually removed by jumbo squid fisheries. Copyright © 2014 Elsevier Inc. All rights reserved.

Major, Trace, and Volatile (CO2, H2O, S, F, and Cl) Elements from 1000+ Hawaiian Olivine-hosted Melt Inclusions Reveal the Dynamics of Crustal Recycling

NASA Astrophysics Data System (ADS)

Marske, J. P.; Hauri, E. H.; Trusdell, F.; Garcia, M. O.; Pietruszka, A. J.

2015-12-01

Global cycling of volatile elements (H2O, CO2, F, S, Cl) via subduction to deep mantle followed by entrainment and melting within ascending mantle plumes is an enigmatic process that controls key aspects of hot spot volcanism (i.e. melting rate, magma supply, degassing, eruptive style). Variations in radiogenic isotope ratios (e.g.187Os/188Os) at hot spots such as Hawaii reveal magmatic processes within deep-seated mantle plumes (e.g. mantle heterogeneity, lithology, and melt transport). Shield-stage lavas from Hawaii likely originate from a mixed plume source containing peridotite and recycled oceanic crust (pyroxenite) based on variations of radiogenic isotopes. Hawaiian lavas display correlations among isotopes, major and trace elements [1] that might be expected to have an expression in the volatile elements. To investigate this link, we present Os isotopic ratios (n=51), and major, trace, and volatile elements from 1003 olivine-hosted melt inclusions (MI) and their host minerals from tephra from Koolau, Mauna Loa, Hualalai, Kilauea, and Loihi volcanoes. The data show a strong correlation between MI volatile contents and incompatible trace element ratios (La/Yb) with Os isotopes of the same host olivines and reveal large-scale volatile heterogeneity and zonation exists within the Hawaiian plume. 'Loa' chain lavas, which are thought to originate from greater proportions of recycled oceanic crust/pyroxenite, have MIs with lower H2O, S, F, and Cl contents compared to 'Kea' chain lavas that were derived from more peridotite-rich sources. The depletion of volatile elements in the 'Loa' volcano MIs can be explained if they tapped an ancient dehydrated oceanic crust component within the Hawaiian plume. Higher extents of melting beneath 'Loa' volcanoes can also explain these depletions. The presence of dehydrated recycled mafic material in the plume source suggests that subduction effectively devolatilizes part of the oceanic crust. These results are similar to the observed shifts in H2O/Ce ratios near the Easter and Samoan hotspots [2,3]. Thus, it appears that multiple hotspots may record relative H2O depletions and possibly other volatiles. [1] Hauri et al. 1996, Nature 382, 415-419. [2] Dixon et al. 2002, Nature 420:385-89 [3] Workman et al. 2006, EPSL 241:932-51.

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

Chemical and seismological constraints on mantle heterogeneity.

PubMed

Helffrich, George

2002-11-15

Recent seismological studies that use scattered waves to detect heterogeneities in the mantle reveal the presence of a small, distributed elastic heterogeneity in the lower mantle which does not appear to be thermal in nature. The characteristic size of these heterogeneities appears to be ca. 8 km, suggesting that they represent subducted recycled oceanic crust. With this stimulus, old ideas that the mantle is heterogeneous in structure, rather than stratified, are reinterpreted and a simple, end-member model for the heterogeneity structure is proposed. The volumetrically largest components in the model are recycled oceanic crust, which contains the heat-producing elements, and mantle depleted of these and other incompatible trace elements. About 10% of the mantle's mass is made up of recycled oceanic crust, which is associated with the observed small-scale seismic heterogeneity. The way this heterogeneity is distributed is in convectively stretched and thinned bodies ranging downwards in size from 8 km. With the present techniques to detect small bodies through scattering, only ca. 55% of the mantle's small-scale heterogeneities are detectable seismically.

Homogenisation of sulphide inclusions within diamonds: A new approach to diamond inclusion geochemistry

NASA Astrophysics Data System (ADS)

McDonald, Iain; Hughes, Hannah S. R.; Butler, Ian B.; Harris, Jeffrey W.; Muir, Duncan

2017-11-01

Base metal sulphide (BMS) inclusions in diamonds provide a unique insight into the chalcophile and highly siderophile element composition of the mantle. Entombed within their diamond hosts, these provide a more robust (closed system) sample, from which to determine the trace element, Re-Os and S-isotopic compositions of the mantle than mantle xenoliths or orogenic peridotites, as they are shielded from alteration during ascent to the Earth's crust and subsequent surface weathering. However, at temperatures below 1100 °C some BMS inclusions undergo subsolidus re-equilibration from an original monosulphide solid solution (Mss) and this causes fractionation of the major and trace elements within the inclusions. Thus to study the subjects noted above, current techniques require the entire BMS inclusion to be extracted for analyses. Unfortunately, 'flaking' of inclusions during break-out is a frequent occurrence and hence the risk of accidentally under-sampling a portion of the BMS inclusion is inherent in current practices. This loss may have significant implications for Re-Os isotope analyses where incomplete sampling of a Re-rich phase, such as chalcopyrite that typically occurs at the outer margins of BMS inclusions, may induce significant bias in the Re-Os and 187Os/188Os measurements and resulting model and isochron ages. We have developed a method for the homogenisation of BMS inclusions in diamond prior to their break-out from the host stone. Diamonds are heated to 1100 °C and then quenched to chemically homogenise any sulphide inclusions for both major and trace elements. Using X-ray Computed Microtomography (μCT) we determine the shape and spatial setting of multiple inclusions within a host stone and crucially show that the volume of a BMS inclusion is the same both before and after homogenisation. We show that the homogenisation process significantly reduces the inherent variability of in situ analysis when compared with unhomogenised BMS, thereby widening the scope for multiple methods for quantitative analysis, even on 'flakes' of single BMS inclusions. Finally we show that the trace elements present in peridotite (P-type) and eclogitic (E-type) BMS are distinct, with P-type diamonds having systematically higher total platinum-group element (particularly Os, Ir, Ru) and Te and As concentrations. These distinctions suggest that the PGE and semi-metal budgets of mantle-derived partial melts will be significantly dependent upon the type(s) and proportions of sulphides present in the mantle source.

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.

Origin and evolution of primitive melts from the Debunscha Maar, Cameroon: Consequences for mantle source heterogeneity within the Cameroon Volcanic Line

NASA Astrophysics Data System (ADS)

Ngwa, Caroline N.; Hansteen, Thor H.; Devey, Colin W.; van der Zwan, Froukje M.; Suh, Cheo E.

2017-09-01

Debunscha Maar is a monogenetic volcano forming part of the Mt. Cameroon volcanic field, located within the Cameroon Volcanic Line (CVL). Partly glassy cauliflower bombs have primitive basanite-picrobasalt compositions and contain abundant normally and reversely zoned olivine (Fo 77-87) and clinopyroxene phenocrysts. Naturally quenched melt inclusions in the most primitive olivine phenocrysts show compositions which, when corrected for post-entrapment modification, cover a wide range from basanite to alkali basalt (MgO 6.9-11.7 wt%), and are generally more primitive than the matrix glasses (MgO 5.0-5.5 wt%) and only partly fall on a common liquid line of descent with the bulk rock samples and matrix glasses. Melt inclusion trace element compositions lie on two distinct geochemical trends: one (towards high Ba/Nb) is thought to represent the effect of various proportions of anhydrous lherzolite and amphibole-bearing peridotite in the source, while the other (for example, high La/Y) reflects variable degrees of partial melting. Comparatively low fractionation-corrected CaO in the melt inclusions with the highest La/Y suggests minor involvement of a pyroxenite source component that is only visible at low degrees of melting. Most of the samples show elevated Gd/Yb, indicating up to 8% garnet in the source. The range of major and trace elements represented by the melt inclusions covers the complete geochemical range given by basalts from different volcanoes of the Cameroon volcanic line, indicating that geochemical signatures that were previously thought to be volcano-specific in fact are probably present under all volcanoes. Clinopyroxene-melt barometry strongly indicates repeated mixing of compositionally diverse melts within the upper mantle at 830 ± 170 MPa prior to eruption. Mantle potential temperatures estimated for the primitive melt inclusions suggest that the thermal influence of a mantle plume is not required to explain the magma petrogenesis.

Large Calcium Isotopic Variation in Peridotitic Xenoliths from North China Craton

NASA Astrophysics Data System (ADS)

Huang, S.; Zhao, X.; Zhang, Z.

2016-12-01

Calcium is the fifth most abundant element in the Earth. The Ca isotopic composition of the Earth is important in many aspects, ranging from tracing the Ca cycle on the Earth to comparing the Earth to other terrestrial planets. There is large mass-dependent Ca isotopic variation, measured as δ44/40Ca relative to a standard sample, in terrestrial igneous rocks: about 2 per mil in silicate rocks, compared to 3 per mil in carbonates. Therefore, a good understanding of the Ca isotopic variation in igneous rocks is necessary. Here we report Ca isotopic data on a series of peridotitic xenoliths from North China Craton (NCC). There is about 1 per mil δ44/40Ca variation in these NCC peridotites: The highest δ44/40Ca is close to typical mantle values, and the lowest δ44/40Ca is found in an Fe-rich peridotite, -1.13 relative to normal mantle (or -0.08 on the SRM 915a scale). This represents the lowest δ44/40Ca value ever reported for igneous rocks. Combined with published Fe isotopic data on the same samples, our data show a positive linear correlation between δ44/40Ca and δ57/54Fe in NCC peridotites. This trend is inconsistent with mixing a low-δ44/40Ca and -δ57/54Fe sedimentary component with a normal mantle component. Rather, it is best explained as the result of kinetic isotopic effect caused by melt-peridotite reaction on a time scale of several hundreds of years. In detail, basaltic melt reacts with peridotite, replaces orthopyroxene with clinopyroxene, and increases the Fo number of olivine. Consistent with this interpretation, our on-going Mg isotopic study shows that low-δ44/40Ca and -δ57/54Fe NCC peridotites also have heavier Mg isotopes compared to normal mantle. Our study shows that mantle metasomatism plays an important role generating stable isotopic variations within the Earth's mantle.

Age and geochemistry of the Newania dolomite carbonatites, India: implications for the source of primary carbonatite magma

NASA Astrophysics Data System (ADS)

Ray, Jyotiranjan S.; Pande, Kanchan; Bhutani, Rajneesh; Shukla, Anil D.; Rai, Vinai K.; Kumar, Alok; Awasthi, Neeraj; Smitha, R. S.; Panda, Dipak K.

2013-12-01

The Newania carbonatite complex of India is one of the few dolomite-dominated carbonatites of the world. Intruding into Archean basement gneisses, the rocks of the complex have undergone limited diversification and are not associated with any alkaline silicate rock. Although the magmatic nature of the complex was generally accepted, its age of emplacement had remained equivocal because of the disturbed nature of radioisotope systems. Many questions about the nature of its mantle source and mode of origin had remained unanswered because of lack of geochemical and isotopic data. Here, we present results of our effort to date the complex using 147Sm-143Nd, 207Pb-206Pb and 40Ar-39Ar dating techniques. We also present mineral chemistry, major and trace element geochemistry and Sr-Nd isotopic ratio data for these carbonatites. Our age data reveal that the complex was emplaced at ~1,473 Ma and parts of it were affected by a thermal event at ~904 Ma. The older 207Pb-206Pb ages reported here (~2.4 Ga) and by one earlier study (~2.3 Ga; Schleicher et al. Chem Geol 140:261-273, 1997) are deemed to be a result of heterogeneous incorporation of crustal Pb during the post-emplacement thermal event. The thermal event had little effect on many magmatic signatures of these rocks, such as its dolomite-magnesite-ankerite-Cr-rich magnetite-magnesio-arfvedsonite-pyrochlore assemblage, mantle like δ13C and δ18O and typical carbonatitic trace element patterns. Newania carbonatites show fractional crystallization trend from high-Mg to high-Fe through high-Ca compositions. The least fractionated dolomite carbonatites of the complex possess very high Mg# (≥80) and have similar major element oxide contents as that of primary carbonatite melts experimentally produced from peridotitic sources. In addition, lower rare earth element (and higher Sr) contents than a typical calcio-carbonatite and mantle like Nb/Ta ratios indicate that the primary magma for the complex was a magnesio-carbonatite melt and that it was derived from a carbonate bearing mantle. The Sr-Nd isotopic data suggest that the primary magma originated from a metasomatized lithospheric mantle. Trace element modelling confirms such an inference and suggests that the source was a phlogopite bearing mantle, located within the garnet stability zone.

Lead isotope evolution across the Neoproterozoic boundary between craton and juvenile crust, Bayuda Desert, Sudan

NASA Astrophysics Data System (ADS)

Evuk, David; Lucassen, Friedrich; Franz, Gerhard

2017-11-01

Metaigneous mafic and ultramafic rocks from the juvenile Neoproterozoic Arabian Nubian Shield (ANS) and the Proterozoic, reworked Saharan Metacraton (SMC) have been analysed for major- and trace elements and Sr, Nd, and Pb isotopes. Most of the rocks are amphibolites metamorphosed at amphibolite facies conditions, some with relicts of a granulite facies stage. The other rocks are metapyroxenites, metagabbros, and some ultramafic rocks. Trace element compositions of the metabasaltic (dominantly tholeiitic) rocks resemble the patterns of island arcs and primitive lavas from continental arcs. Variable Sr and Nd isotope ratios indicate depleted mantle dominance for most of the samples. 207Pb/204Pb signatures distinguish between the influence of high 207Pb/204Pb old SMC crust and depleted mantle signatures of the juvenile ANS crust. The Pb isotope signatures for most metabasaltic rocks, metapyroxenites and metagabbros from SMC indicate an autochthonous formation. The interpretation of the new data together with published evidence from mafic xenoliths on SMC and ophiolite from ANS allows an extrapolation of mantle evolution in time. There are two lines of evolution in the regional mantle, one, which incorporates potential upper crust material during Neoproterozoic, and a second one with a depleted mantle signature since pre-Neoproterozoic that still is present in the Red Sea and Gulf of Aden spreading centres.

Metasomatic Reaction Zones as Monitors of Trace Element Transfer at the Slab-Mantle Interface: the Case of the Hochwart Peridotite (Ulten Zone, Italy)

NASA Astrophysics Data System (ADS)

Marocchi, M.; Hermann, J.; Bargossi, G. M.; Mair, V.; Morten, L.

2006-12-01

Ultramafic blocks belonging to the Hochwart peridotite outcrop (Ulten Zone, Italian Alps) preserve a series of metasomatic mineral zones generated by infiltration of Si-rich hydrous fluids which occurred at the gneiss- peridotite interface. The age of the high pressure metamorphism for the Hochwart complex has been constrained at 330 Ma (Tumiati et al., 2003, EPSL, 210, 509-526). The country rocks are stromatic gneisses consisting mainly of quartz, K-feldspar, garnet, kyanite, biotite and muscovite. The ultramafic body consists of strongly serpentinized metaperidotites which are exposed as a hectometre-size lens along a steep gully, associated to monomineralic zones that developed at the contact between the peridotite body and the garnet gneiss country rocks. The composition of the metasomatic zones has been investigated in detail and records an order of metasomatic zoning formed by phlogopite-rich to tremolite-anthophyllite-rich rocks going from the host gneiss towards the peridotite. In some cases, the ultramafics fade into the gneisses developing serpentine and talc which has replaced, presumably at lower temperatures, the serpentine matrix and occurs in association with chlorite. Phlogopite aggregates (phlogopitite) with accessory minerals (quartz + zircon + apatite) and metabasic pods (phlogopite and hornblende) also occur. Black tourmaline (schorl-dravite solid solution) has been found for the first time in the contact near the phlogopite zone, suggesting an external addition of elements (boron and fluorine) to the system at high temperature. The formation of the metasomatic zones composed exclusively of hydrous phases must have involved extensive H2O-metasomatism as already documented for the Ulten peridotites. The source for these fluids can be a system of trondhjemitic-pegmatitic dikes cutting the peridotite that would have channelled aqueous fluids into the ultramafic rocks. Whole-rock geochemistry and trace element (LA ICP-MS) composition of hydrous phases (phlogopite and amphibole) in different metasomatic zones indicate mobility of many elements, including elements such as Ta which are considered to have scarce mobility in fluids. Trace element composition of accessory minerals in the phlogopite-rich zone suggests that the trace element signature of subduction zone fluids may be fractionated in this zone. The progressive depletion in some trace elements (LREE) and enrichment in LILE and Li from the peridotite towards the gneiss suggests a strong influence of bulk composition on the trace element budget of hydrous minerals. Since the ultramafic blocks can be representative of metasomatic processes occurring at the slab-mantle interface, we can infer that metasomatic reactions between slab-derived fluids and ultramafic mantle wedge will follow a specific series of reactions, creating mineral zonation similar to those observed in this study. Our results further favour the evidence that the primary composition of subduction zone fluids is modified substantially by metasomatic reactions occurring in the mantle wedge.

In Situ Trace Element Analysis of an Allende Type B1 CAI: EK-459-5-1

NASA Technical Reports Server (NTRS)

Jeffcoat, C. R.; Kerekgyarto, A.; Lapen, T. J.; Andreasen, R.; Righter, M.; Ross, D. K.

2014-01-01

Variations in refractory major and trace element composition of calcium, aluminum-rich inclusions (CAIs) provide constraints on physical and chemical conditions and processes in the earliest stages of the Solar System. Previous work indicates that CAIs have experienced complex histories involving, in many cases, multiple episodes of condensation, evaporation, and partial melting. We have analyzed major and trace element abundances in two core to rim transects of the melilite mantle as well as interior major phases of a Type B1 CAI (EK-459-5-1) from Allende by electron probe micro-analyzer (EPMA) and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to investigate the behavior of key trace elements with a primary focus on the REEs Tm and Yb.

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.

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.

Geochemistry of lavas from Taal volcano, southwestern Luzon, Philippines: evidence for multiple magma supply systems and mantle source heterogeneity

USGS Publications Warehouse

Miklius, Asta; Flower, M.F.J.; Huijsmans, J.P.P.; Mukasa, S.B.; Castillo, P.

1991-01-01

Taal lava series can be distinguished from each other by differences in major and trace element trends and trace element ratios, indicating multiple magmatic systems associated with discrete centers in time and space. On Volcano Island, contemporaneous lava series range from typically calc-alkaline to iron-enriched. Major and trace element variation in these series can be modelled by fractionation of similar assemblages, with early fractionation of titano-magnetite in less iron-enriched series. However, phase compositional and petrographic evidence of mineral-liquid disequilibrium suggests that magma mixing played an important role in the evolution of these series. -from Authors

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.

Subduction and melting processes inferred from U-Series, Sr Nd Pb isotope, and trace element data, Bicol and Bataan arcs, Philippines

NASA Astrophysics Data System (ADS)

DuFrane, S. Andrew; Asmerom, Yemane; Mukasa, Samuel B.; Morris, Julie D.; Dreyer, Brian M.

2006-07-01

We present U-series, Sr-Nd-Pb isotope, and trace element data from the two principal volcanic chains on Luzon Island, developed over oppositely dipping subduction zones, to explore melting and mass transfer processes beneath arcs. The Bataan (western) and Bicol (eastern) arcs are currently subducting terrigenous and pelagic sediments, respectively, which have different trace element and isotopic compositions. The range of ( 230Th/ 238U) disequilibria for both arcs is 0.85-1.15; only lavas from Mt. Mayon (Bicol arc) have 230Th activity excesses. Bataan lavas have higher 87Sr/ 86Sr and lower 143Nd/ 144Nd than Bicol lavas ( 87Sr/ 86Sr = 0.7042-0.7046, 143Nd/ 144Nd = 0.51281-0.51290 vs. 87Sr/ 86Sr = 0.70371-0.70391, 143Nd/ 144Nd = 0.51295-0.51301) and both arcs show steep linear arrays towards sediment values on 207Pb/ 204Pb vs. 206Pb/ 204Pb diagrams. Analysis of incompatible element and isotopic data allows identification of a sediment component that, at least in part, was transferred as a partial melt to the mantle wedge peridotite. Between 1% and 5% sediment melt addition can explain the isotopic and trace element variability in the rocks from both arcs despite the differences in sediment supply. We therefore propose that sediment transfer to the mantle wedge is likely mechanically or thermally limited. It follows that most sediments are either accreted, reside in the sub-arc lithosphere, or are recycled into the convecting mantle. However, whole-sale sediment recycling into the upper mantle is unlikely in light of the global mid-ocean ridge basalt data. Fluid involvement is more difficult to characterize, but overall the Bicol arc appears to have more fluid influence than the Bataan arc. Rock suites from each arc can be related by a dynamic melting process that allows for 230Th ingrowth, either by dynamic or continuous flux melting, provided the initial ( 230Th/ 232Th) of the source is ˜0.6-0.7. The implication of either model is that inclined arrays on the U-Th equiline diagram may not have chronologic significance. Modeling also suggests that U-series disequilibria are influenced by the tectonic convergence rate, which dictates mantle matrix flow. Thus with slower matrix flow there is a greater degree of 230Th ingrowth. While other factors such as prior mantle depletion and addition of a subducted component may explain some aspects of U-series data, an overall global correlation between tectonic convergence rate and the extent of U-Th disequilibria may originate from melting processes.

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.

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.

Composition of the earth's upper mantle-I. Siderophile trace elements in ultramafic nodules

USGS Publications Warehouse

Morgan, J.W.; Wandless, G.A.; Petrie, R.K.; Irving, A.J.

1981-01-01

Seven siderophile elements (Au, Ge, Ir, Ni, Pd, Os, Re) were determined by radiochemical neutron activation analysis in 19 ultramafic rocks, which are spinel lherzollites-xenoliths from North and Central America, Hawaii and Australia, and garnet Iherzolitexenoliths from Lesotho. Abundances of the platinum metals are very uniform in spinel lherzolites averaging 3.4 ?? 1.2 ppb Os, 3.7 ?? 1.1 ppb Ir, and 4.6 ?? 2.0 ppb Pd. Sheared garnet lherzolite PHN 1611 has similar abundances of these elements, but in 4 granulated garnet lherzolites, abundances are more variable. In all samples, the Pt metals retain cosmic ( Cl-chondrite) ratios. Abundances of Au and Re vary more than those of Pt metals, but the Au/Re ratio remains close to the cosmic value. The fact that higher values of Au and Re approach cosmic proportions with respect to the Pt metals, suggests that Au and Re have been depleted in some ultramafic rocks from an initially chondrite-like pattern equivalent to about 0.01 of Cl chondrite abundances. The relative enrichment of Au and Re in crustal rocks is apparently the result of crust-mantle fractionation and does not require a special circumstance of core-mantle partitioning. Abundances of moderately volatile elements Ni, Co and Ge are very uniform in all rocks, and are much higher than those of the highly siderophile elements Au, Ir, Pd, Os and Re. When normalized to Cl chondrites, abundances of Ni and Co are nearly identical, averaging 0.20 ?? 0.02 and 0.22 ?? 0.02, respectively; but Ge is only 0.027 ?? 0.004. The low abundance of Ge relative to Ni and Co is apparently a reflection of the general depletion of volatile elements in the Earth. The moderately siderophile elements cannot be derived from the same source as the highly siderophile elements because of the marked difference in Cl chondrite-normalized abundances and patterns. We suggest that most of the Ni, Co and Ge were enriched in the silicate by the partial oxidation of pre-existing volatile-poor Fe-Ni, whereas the corresponding highly siderophile elements remained sequestered by the surviving metal. The highly siderophile elements may have been introduced by a population of ~103 large (~1022 g) planetisimals, similar to those forming the lunar mare basins. ?? 1981.

Mantle dynamics and generation of a geochemical mantle boundary along the East Pacific Rise - Pacific/Antarctic ridge

NASA Astrophysics Data System (ADS)

Zhang, Guo-Liang; Chen, Li-Hui; Li, Shi-Zhen

2013-12-01

A large-scale mantle compositional discontinuity was identified along the East Pacific Rise (EPR) and the Pacific-Antarctic Ridge (PAR) with an inferred transition located at the EPR 23°S-32°S. Because of the EPR-Easter hotspot interactions in this area, the nature of this geochemical discontinuity remains unclear. IODP Sites U1367 and U1368 drilled into the ocean crust that was accreted at ∼33.5 Ma and ∼13.5 Ma, respectively, between 28°S and 30°S on the EPR. We use lavas from Sites U1367 and U1368 to track this mantle discontinuity away from the EPR. The mantle sources for basalts at Sites U1367 and U1368 represent, respectively, northern and southern Pacific mantle sub-domains in terms of Sr-Nd-Pb-Hf isotopes. The significant isotopic differences between the two IODP sites are consistent with addition of ancient subduction-processed ocean crust to the south Pacific mantle sub-domain. Our modeling result shows that a trace element pattern similar to that of U1368 E-MORB can be formed by melting a subduction-processed typical N-MORB. The trace element and isotope compositions for Site U1368 MORBs can be formed by mixing a HIMU mantle end-member with Site U1367 MORBs. Comparison of our data with those from the EPR-PAR shows a geochemical mantle boundary near the Easter microplate that separates the Pacific upper mantle into northern and southern sub-domains. On the basis of reconstruction of initial locations of the ocean crust at the two sites, we find that the mantle boundary has moved northward to the Easter microplate since before 33.5 Ma. A model, in which along-axis asthenospheric flow to where asthenosphere consumption is strongest, explains the movement of the apparent mantle boundary.

Minor and trace element geochemistry of volcanic rocks dredged from the Galapagos spreading center: role of crystal fractionation and mantle heterogeneity.

USGS Publications Warehouse

Clague, D.A.; Frey, F.A.; Thompson, G.; Rindge, S.

1981-01-01

A wide range of rock types (abyssal tholeiite, Fe-Ti-rich basalt, andesite, and rhyodacite) were dredged from near 95oW and 85oW on the Galapagos spreading center. Computer modeling of major element compositions has shown that these rocks could be derived from common parental magmas by successive degrees of fractional crystallization. However, the P2O5/K2O ratio implies distinct mantle source compositions for the two areas. These source regions also have different rare earth element (REE) abundance patterns. The sequence of fractionated lavas differs for the two areas and indicates earlier fractionation of apatite and titanomagnetite in the lavas from 95oW. The mantle source regions for these two areas are interpreted to be depleted in incompatible (and volatile?) elements, although the source region beneath 95oW is less severely depleted in La and K. -Authors

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.

N-MORB crust beneath Fuerteventura in the easternmost part of the Canary Islands: evidence from gabbroic xenoliths

NASA Astrophysics Data System (ADS)

Neumann, Else-Ragnhild; Vannucci, Riccardo; Tiepolo, Massimo

2005-09-01

Gabbro xenoliths reported in this paper were collected in northern Fuerteventura, the Canary Island located closest to the coast of Africa. The xenoliths are very fresh and consist of Ti-Al-poor clinopyroxene + plagioclase (An87-67) + olivine (Fo72-86) ± orthopyroxene. Clinopyroxene and orthopyroxene are constantly and markedly depleted in light rare earth elements (LREE) relative to heavy REE (HREE), as expected for cumulus minerals formed from highly refractory N-MORB-type melts. In contrast, whole-rock Primordial Mantle-normalized trace element patterns range from mildly S-shaped (mildly depleted in Pr-Sm relative to both the strongly incompatible elements Rb-La and the HREE) to enriched. Estimates show that the trace element compositions of the rocks and their minerals are compatible with formation as N-MORB gabbro cumulates, which have been infiltrated at various extents (≤1% to >5%) by enriched alkali basaltic melts. The enriched material is mainly concentrated along grain boundaries and cracks through mineral grains, suggesting that the infiltration is relatively recent, and is thus associated with the Canary Islands magmatism. Our data contradict the hypothesis that a mantle plume was present in this area during the opening of the Atlantic Ocean. No evidence of continental material that might reflect attenuated continental crust in the area has been found. Gabbro xenoliths with REE and trace element compositions similar to those exhibited by the Fuerteventura gabbros are also found among gabbro xenoliths from the islands of La Palma (western Canary Islands) and Lanzarote. The compositions of the most depleted samples from these islands are closely similar, implying that there was no significant change in chemistry during the early stages of formation of the Atlantic oceanic crust in this area. Strongly depleted gabbros similar to those collected in Fuerteventura have also been retrieved in the MARK area along the central Mid-Atlantic Ridge. The presence of N-MORB oceanic crust beneath Fuerteventura implies that the continent-ocean transition in the Canary Islands area must be relatively sharp, in contrast to the situation both further north along the coast of Morocco, and along the Iberian peninsula.

Volatile transfer and recycling at convergent margins: Mass-balance and insights from high-P/T metamorphic rocks

NASA Astrophysics Data System (ADS)

Bebout, Gray E.

The efficiency with which volatiles are deeply subducted is governed by devolatilization histories and the geometries and mechanisms of fluid transport deep in subduction zones. Metamorphism along the forearc slab-mantle interface may prevent the deep subduction of many volatile components (e.g., H2O, Cs, B, N, perhaps As, Sb, and U) and result in their transport in fluids toward shallower reservoirs. The release, by devolatilization, and transport of such components toward the seafloor or into the forearc mantle wedge, could in part explain the imbalances between the estimated amounts of subducted volatiles and the amounts returned to Earth's surface. The proportion of the initially subducted volatile component that is retained in rocks subducted to depths greater than those beneath magmatic arcs (>100 km) is largely unknown, complicating assessments of deep mantle volatile budgets. Isotopic and trace element data and volatile contents for the Catalina Schist, the Franciscan Complex, and eclogite-facies complexes in the Alps (and elsewhere) provide insight into the nature and magnitude of fluid production and transport deep in subduction zones and into the possible effects of metamorphism on the compositions of subducting rocks. Compatibilities of the compositions of the subduction-related rocks and fluids with the isotopic and trace element compositions of various mantle-derived materials (igneous rocks, xenoliths, serpentinite seamounts) indicate the potential to trace the recycling of rock and fluid reservoirs chemically and isotopically fractionated during subduction-zone metamorphism.

SrNdPb isotopic and trace element evidence for crustal contamination of plume-derived flood basalts: Oligocene flood volcanism in western Yemen

NASA Astrophysics Data System (ADS)

Baker, J. A.; Thirlwall, M. F.; Menzies, M. A.

1996-07-01

Oligocene flood basalts from western Yemen have a relatively limited range in initial isotopic composition compared with other continental flood basalts: 87Sr/86Sr = 0.70365-0.70555 ; 143Nd/144Nd = 0.5129-0.51248 ( ɛNd = +6.0 to -2.4) ; 206pb/204Pb = 17.9-19.3 . Most compositions lie outside the isotopic ranges of temporally and spatially appropriate mantle source compositions observed in this area, i.e., Red Sea/Gulf of Aden MORB mantle, the Afar plume, and Pan-African lithospheric mantle Correlations between indices of fractionation, silica, and isotope ratios suggest that crustal contamination has substantially modified the primary isotopic and incompatible trace element characteristics of the flood basalts. However, significant scatter in these correlations was produced by: (a) the heterogeneous isotopic composition of Pan-African crust; (b) the difference in susceptibility of magmas to contamination as a result of variable incompatible trace element contents in primary melts produced by differing degrees of partial melting; (c) the presence or absence of plagioclase as a fractionating phase generating complex contamination trajectories for Sr; (d) sampling over a wide area not representing a single coherent magmatic system; and (e) variation in contamination mechanisms from assimilation associated with fractionation (AFC) to assimilation by hot mafic magmas with little concomitant fractionation. The presence of plagioclase as a fractionating phase in some suites that were undergoing AFC requires assimilation to have taken place within the crust and, coupled with the limited LREE-enrichment accompanying isotopic variations, excludes the possibility that an AFC-type process took place during magma transfer through the lithospheric mantle. Isotopic compositions of some of the inferred crustal assimilants are similar to those postulated by other workers for an enriched lithospheric mantle source of many flood basalts in southwestern Yemen, Ethiopia, and Djibouti. The western Yemen flood basalts contain 0-30% crust which largely swamps their primary lead isotopic signature, but the primary SrNd isotopic signature is close to that of the least contaminated and isotopically most depleted flood basalts. LREE/HFSE and LILE/HFSE ratios also correlate with isotopic data as a result of crustal contamination. However, Nb/La and K/Nb ratios of >1.1 and <150, respectively, in least contaminated samples require an OIB-like source. The pre-contamination isotopic signature is estimated to be: 87Sr/86Sr ˜ 0.7036; 143Nd/144Nd ˜ 0.51292 ; 206Pb/204Pb ˜ 18.4-19.0 . This, coupled with low LILE/HFSE ratios, suggest the source has characteristics akin to the Afar plume. A mantle source isotopically more depleted than Bulk Earth, but not as depleted as MORB, coupled with LILE depletion, also characterises other examples of plume-derived flood volcanism. This mantle reservoir is responsible for the second largest outbursts of volcanism on Earth and has radiogenic isotopic characteristics akin to PREMA mantle, but the incompatible trace element signature of HIMU mantle.

Mantle ingredients for making the fingerprint of Etna alkaline magmas: implications for shallow partial melting within the complex geodynamic framework of Eastern Sicily

NASA Astrophysics Data System (ADS)

Viccaro, Marco; Zuccarello, Francesco

2017-09-01

Mantle ingredients responsible for the signature of Etnean Na- and K-alkaline magmas and their relationships with short-term geochemical changes of the erupted volcanic rocks have been constrained through a partial melting model that considers major, trace elements and water contents in the produced liquids. Characteristics of the Etnean source for alkaline magmas have been supposed similar to those of the mantle accessible at a regional scale, namely below the Hyblean Plateau. The assumption that the Etnean mantle resembles the one beneath the Hyblean Plateau is justified by the large geochemical affinities of the Etnean hawaiites/K-trachybasalts and the Hyblean hawaiites/alkali basalts for what concerns both trace elements and isotope systematics. We have modeled partial melting of a composite source constituted by two rock types, inferred by lithological and geochemical features of the Hyblean xenoliths: 1) a spinel lherzolite bearing metasomatic, hydrous phases and 2) a garnet pyroxenite in form of veins intruded into the spinel lherzolite. The partial melting modeling has been applied to each rock type and the resulting primary liquids have been then mixed in various proportions. These compositions have been compared with some Etnean alkaline magmas of the post ∼60 ka activity, which were firstly re-equilibrated to mantle conditions through mass balance calculations. Our results put into evidence that concentrations of major and trace elements along with the water obtained from the modeling are remarkably comparable with those of Etnean melts re-equilibrated at primary conditions. Different proportions of the spinel lherzolite with variable modal contents of metasomatic phases and of the garnet pyroxenite can therefore account for the signature of a large spectrum of Etnean alkaline magmas and for their geochemical variability through time, emphasizing the crucial role played by compositional small-scale heterogeneity of the source. These heterogeneities are able to produce magmas with variable compositions and volatile contents, which can then undergo distinct histories of ascent and evolution, leading to the wide range of eruptive styles observed at Mt. Etna volcano. Being partial melting confined in the spinel facies of the mantle, our model implies that the source of Mt. Etna magmas might be rather shallow (<2 GPa; i.e., lesser than ca. 60 km), excluding the presence of deep, plume-like mantle structures responsible for magma generation. Partial melting should occur consequently as a response of mantle decompression within the framework of regional tectonics affecting the Eastern Sicily, which could be triggered by extensional tectonics and/or subduction-induced mantle upwelling.

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.

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.

The infrared signature of water associated with trivalent cations in olivine

NASA Astrophysics Data System (ADS)

Berry, Andrew J.; O'Neill, Hugh St. C.; Hermann, Jörg; Scott, Dean R.

2007-09-01

Forsterite crystals were synthesised under water saturated conditions at 1400 °C and 1.5 GPa doped with trace amounts of either B, Al, Sc, Ti, V, Cr, Mn, Fe, Co, Ga, Y, Zr, In, Sm, Gd, Dy, Tm, or Lu. The common and intense hydroxyl stretching bands in the infrared spectra of spinel peridotite olivine, at 3572 and 3525 cm -1, were only reproduced in the presence of Ti. Those samples where the trace element substitutes as the trivalent cation on the Mg 2+ site were identified from a systematic variation in concentration with the trivalent ionic radius. The hydroxyl region of all samples is essentially identical except for between 3300 and 3400 cm -1. This region is characterised by one or more bands, with the energy of the most intense feature being correlated with the ionic radius of the trivalent cation. The integrated intensity of these hydroxyl bands also correlates with the concentration of the trivalent cation. These correlations provide unambiguous evidence that bands, or peaks, in this region correspond to water at defect sites associated with trivalent cations. "Trivalent peaks" are sometimes observed in samples of mantle olivine and most likely indicate water associated with Fe 3+. The water at this site is not incorporated under normal mantle conditions and should not be included in estimates of the water capacity of mantle olivine. These results emphasise the importance of identifying the infrared signature of different water substitution mechanisms.

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.

Volatile, Trace Element and Isotopic Variations of Mafic Arc Volcanic Rocks from Nicaragua and Costa Rica

NASA Astrophysics Data System (ADS)

Hoernle, K.; Sadofsky, S.; Nichols, H.; Portnyagin, M.; van den Bogaard, P.; Alvarado, G.

2003-12-01

Quaternary volcanic rocks from the Central American Volcanic Arc in central Nicaragua and central Costa Rica exhibit major differences in their volatile, trace element and isotopic compositions. Olivine-hosted melt inclusions in Nicaraguan volcanic rocks with high Fo contents (>73) extend to high H2O (up to 5.3%), S (10-6860 ppm) and Cl (490-2340 ppm) contents. The volcanic rocks have high ratios of fluid mobile to fluid immobile elements such as Ba/La (65-122), Ba/Th (484-1304) and U/La (0.08-0.17). Additionally, they have 143Nd/144Nd (0.51300-0.51307) similar to normal mid-ocean-ridge basalts (N-MORB) from the East Pacific Rise (EPR), but 87Sr/86Sr (0.7035-0.7042) ratios are much higher than those found in fresh EPR glasses. Pb isotopic compositions of the samples (e.g. 206Pb/204Pb = 18.5-19.0, 207Pb/204Pb = 15.52-15.58) form an array between EPR basalts and subducted sediments. The volatile, trace element and isotope data are consistent with mixing of fluids highly enriched in fluid-mobile elements from subducted sediments with a N-MORB-type mantle wedge to produce the Nicaraguan volcanic rocks. In contrast, olivine-hosted melt inclusions (Fo >82) in Costa Rican volcanic rocks show a similar range in H2O (up to 5.1%) to Nicaraguan inclusions but overall have lower S (0-1340 ppm) and Cl (10-790 ppm) contents. Costa Rican lavas also have lower Ba/La (7-35), Ba/Th (55-338), U/La (0.02-0.12), 87Sr/86Sr (0.7035-0.7038) and 143Nd/144Nd (0.51292-0.51301) than Nicaraguan lavas, but 87Sr/86Sr and Pb isotope ratios (e.g. 206Pb/204Pb = 19.02-19.32) are more radiogenic than in Nicaragua and than usually found in fresh EPR MORB. Our data are consistent with the presence of Galapagos Hotspot-type components in the source of the central Costa Rican volcanic rocks, derived from the subducting Galapagos Hotspot Track and from Galapagos-type material entering the mantle wedge through a slab tear or window (Abratis and Worner, 2000; Geology). The estimated volume of volcanic rocks erupted in the last 100,000 years (Carr et al., 1990, Contrib. Min. Pet.; in press, AGU Spec. Pub.) are substantially higher in central Costa Rica than in Nicaragua, suggesting greater productivity of melting beneath Costa Rica. Since the flux of hydrous fluids appears to be similar beneath both arc segments, higher melt productivity beneath Costa Rica could reflect the presence of larger volumes of more fertile, hotter Galapagos-type mantle upwelling through a slab tear or window into the Costa Rican mantle wedge.

Composition of the lithospheric mantle in the Siberian craton : New constraints from fresh peridotites from the Udachnaya-East Kimberlite

NASA Astrophysics Data System (ADS)

Doucet, Luc-Serge; Ionov, Dmitri A.; Ashchepkov, Igor

2010-05-01

Peridotite xenoliths from the Udachnaya kimberlite pipe represent the major source of lithospheric mantle samples beneath central Siberian craton. An important problem with the availble data [1], however, is that the Udachnaya xenoliths, like many other kimberlite-hosted peridotite suites worldwide, are extensively altered due to interaction with host magma and post-eruption alteration. This alteration causes particular dificulties for whole-rock studies including microstructures, modal estimates and chemical compositions. We report petrographic data and major and trace element compositions for whole-rocks and minerals of some 30 unusually fresh peridotite xenolith from the Udachnaya-East kimberlite. Our study has two goals. The first is to present and discuss trace element data on rocks and minerals from Udachnaya, whose composition remains little known. The other one is to explore how the availability of the fresh peridotites improves our knowledge of petrology and geochemistry of cratonic mantle in relation to published data on altered samples [1]. The xenoliths are spinel, garnet-spinel and garnet facies peridotites including garnet- and cpx-rich lherzolites, garnet and spinel harzburgites and dunites. Thermobarometric estimates for garnet bearing rocks yield T = 800-1350°C and P = 20-70 kbar, low-T spinel facies rocks may originate from shallower levels. Thus, the suite represents a lithospheric profile from the sub-Moho mantle down to ~210 km. The deeper peridotites commonly have porphyroclastic microstructures with mainly neoblast olivine, opx porphyroclasts and cpx and garnet with broadly variable morphologies whereas rocks of shallow origin are commonly protogranular. Trace element compositions in bulk rocks appear to be affected by host magma contamination with enrichments in highly to moderately incompatible elements as well as in alkalis. Nevertheless, the kimberlite-related contamination cannot explain a combination of low Th and U and high Sr contents. The broad range of heavy REE appears to be controlled by the presence and the abundance of garnet and is also related to microstructures such that granular spinel harzburgites have lower HREE contents than "fertile" porphyroclastic garnet lherzolites. Trace elements in cpx and garnet have equilibrated patterns in porphyroclastic peridotites and complex sinusoidal shapes in granular peridotites. Bulk-rock major element compositions show important variations in Mg# (0.89 - 0.93), SiO2 (41.5 - 46.6%), Al2O3 (0.3 - 4%) and CaO (0.3 - 4%). As for compatible trace elements, the major element compositions appear to be related to microstructures. Calculated modal compositions show highly variable opx contents (4.5 - 24%), which are generally lower than in Kaapvaal peridotites but are similar to those from the North Atlantic craton [3]. Overall, modal compositions and the contents of low-mobility elements, are consistent with an origin by variable degrees of partial melting of fertile mantle [1-3]. The range in FeO contents (6-8.5%) may indicate either variable melting depths [2] or post-melting enrichments. Enrichments in SiO2 show some similarities to those in supra-subduction xenoliths [4]; enrichments in highly incompatible elements can be explained by metasomatism with possible involvement of subduction-related fluids. Strong correlations between chemical compositions and microstructures indicate the involvement of tectonic processes in melt percolation and metasomatism. We suggest that the cratonic lithosphere in Siberia was formed in three stages: (1) formation of proto-cratonic mantle by high-degree melting at variable depth, (2) accretion of the proto-craton domains in subduction-related settings, (3) metasomatism commonly accompanied by deformation. [1] Boyd et al (1997) Contrib. Mineral. Petrol. 128, 228-246. [2] Herzberg (2004) J. Petrol. 45, 2507-2530. [3] Wittig et al (2008) Lithos 71, 289-322. [4] Ionov (2009) J. Petrol. In press

The geochemical and Sr-Nd-Pb-He isotopic characterization of the mantle source of Rungwe Volcanic Province: comparison with the Afar mantle domain

NASA Astrophysics Data System (ADS)

Castillo, P. R.; Hilton, D. R.; Halldorsson, S. A.; Wang, R.

2012-12-01

The ultimate source of heat and magmatism associated with continental rifting in the East African Rift System (EARS) is generally viewed to be the African Superplume, but there is continuing debate on the surface expression of this large anomalous feature, which originates in the lower mantle. Previous studies have demonstrated an insignificant role for crustal contamination thereby identifying a single mantle plume signature in Quaternary basalts from the Main Ethiopian Rift in the northern EARS. This is designated to be the Afar plume and is characterized by, e.g., 3He/4He >15 RA, 206Pb/204Pb = 19.5 and 87Sr/86Sr = 0.7035 [Rooney et al., J. Pet. 53, 2012]. In contrast, the signature of plume(s) in the southern EARS is less constrained. Rogers et al. [EPSL 176, 2000] proposed a plume in the sub-lithospheric Kenyan mantle with characteristically lower 43Nd/144Nd than the Afar plume whereas Furman [JAES 48, 2007] advocated a high μ [HIMU] plume based primarily on the high 206Pb/204Pb ratios of lavas in all areas within and south of the Turkana Depression: both models assume a 3He/4He lower than the Afar plume. Here we report the trace element and Sr-Nd-Pb isotopic composition of basaltic lavas from the Rungwe Volcanic Province (RVP) in the southern extreme of the Western Rift previously identified as a high 3He/4He locality (~15 RA; [Hilton et al., GRL 38, 2011]). Trace element analyses are within the previously reported range of lava compositions that include a relatively large lithospheric component. More importantly, we identify correlations among incompatible trace element and isotopic ratios (e.g., 3He/4He vs 206Pb/204Pb, Rb/Sr, Nb/Ta; 87Sr/86Sr vs 208Pb/204Pb). Our new results suggest the presence of a distinct, high 3He/4He mantle source beneath RVP that is more radiogenic (e.g., 206Pb/204Pb up to ~19.8; 87Sr/86Sr up to 0.7055) than the Afar mantle plume. There is also very little or no HIMU signature in RPV basalts based on their high Sr and low Nd isotopic ratios.

Geochemical insights into the lithology of mantle sources for Cenozoic alkali basalts in West Qinling, China

NASA Astrophysics Data System (ADS)

Dai, Li-Qun; Zheng, Fei; Zhao, Zi-Fu; Zheng, Yong-Fei

2018-03-01

Although alkali basalts are common in oceanic islands and continental rifts, the lithology of their mantle sources is still controversial. While the peridotite is usually viewed as a common source lithology, there are increasing studies suggesting significant contributions from ultramafic metasomatites such as carbonated peridotite, pyroxenite and hornblendite to the origin of alkali basalts. The present study indicates that carbonated peridotite plus hornblendite would have served as the mantle sources of Cenozoic alkali basalts from the West Qinling orogen in China. The target basalts show low SiO2 contents of 36.9 to 40.8 wt% and highly variable Na2O + K2O contents from 0.86 to 4.77 wt%, but high CaO contents of 12.5 to 16.3 wt% and CaO/Al2O3 ratios of 1.42 to 2.19. They are highly enriched in the majority of incompatible trace elements, but depleted in Rb, K, Pb, Zr, Hf, and Ti. Furthermore, they exhibit high (La/Yb)N, Zr/Hf, Ce/Pb and Nb/Ta ratios, but low Ti/Eu and Hf/Sm ratios. Generally, with increasing (La/Yb)N and CaO/Al2O3 ratios, their Ti/Eu and Hf/Sm ratios decrease whereas their Zr/Hf, Ce/Pb and Nb/Ta ratios increase. These major and trace element features are similar to those of carbonatites and hornblendite-derived melts to some extent, but significantly different from those of mid-ocean ridge basalts (MORB). This suggests that the alkali basalts would be originated from metasomatic mantle sources. A comparison of the major-trace elements in the alkali basalts with those of some representative mantle-derived melts indicates that the source lithology of alkali basalts is a kind of ultramafic metasomatites that are composed of carbonated peridotite and hornblendite. Such metasomatites would be generated by reaction of the depleted MORB mantle peridotite with hydrous, carbonate-bearing felsic melts derived from partial melting of the subducted Paleotethyan oceanic crust. Therefore, the melt-peridotite reaction at the slab-mantle interface in the Paleotethyan subduction channel plays the key role in transferring the geochemical signatures from the subducted Paleotethyan oceanic crust to the alkali basalts in the fossil convergent plate margin.

A Missing Link in Understanding Mantle Wedge Melting, Higashi-akaishi Peridotite, Japan

NASA Astrophysics Data System (ADS)

Till, C. B.; Carlson, R. W.; Grove, T. L.; Wallis, S.; Mizukami, T.

2009-12-01

The Sanbagawa subduction-type metamorphic belt in SW Japan represents the deepest exposed portion of a Mesozoic accretionary complex along the Japanese island arc. Located on the island of Shikoku, the Higashi-akaishi peridotite body is the largest ultramafic lens within the Sanbagawa belt and is dominantly composed of dunite, lherzolite and garnet clinopyroxenite, interfingered in one locality with quartz-rich eclogite. Previous work indicates the P-T history of the peridotite includes rapid prograde metamorphism with peak temperatures of 700-810°C and pressures of 2.9-3.8 GPa at approximately 110-120 Ma. Here we present major and trace element and isotopic data for samples within the Higashi-akaishi peridotite body that suggest it records subduction zone melting processes. Ultramafic samples range from 40-52 wt. % SiO2 and 21-45 wt. % MgO with olivine and clinopyroxene Mg#s as high as 0.93 and have trace element concentrations diagnostic of subduction zone processes. The quartz-rich eclogite contains 62 wt. % SiO2, 6 wt. % MgO and 13 wt. % Al2O3 and has trace element concentrations that are enriched relative to the ultramafic samples. 87Sr/86Sr (.703237-.704288), 143Nd/144Nd (ɛNd=+2-6) and Pb isotopic compositions are within the range of Japanese arc rocks. 187Os/188Os values range from typical mantle values (0.123-0.129), to slightly elevated (0.133) in one peridotite with an unusually low Os content, to a high of 0.145 in the quartz-rich eclogite. The presence of garnet porphyroblasts that enclose primary euhedral chlorite, together with the chemical evidence, suggest these samples are associated with mantle melting in the presence of H2O near their peak P-T conditions and may represent both residues and trapped melts within a paleo-mantle wedge. The peak P-T conditions of these rocks are also similar to the solidus conditions of H2O-saturated fertile mantle based on experimental determinations. Thus the Higashi-akaishi peridotite may be a real world analog to hydrous mantle melting experiments and offer crucial evidence on the mechanisms of melting in the mantle wedge at subduction zones.

Terrestrial magma ocean and core segregation in the earth

NASA Technical Reports Server (NTRS)

Ohtani, Eiji; Yurimoto, Naoyoshi

1992-01-01

According to the recent theories of formation of the earth, the outer layer of the proto-earth was molten and the terrestrial magma ocean was formed when its radius exceeded 3000 km. Core formation should have started in this magma ocean stage, since segregation of metallic iron occurs effectively by melting of the proto-earth. Therefore, interactions between magma, mantle minerals, and metallic iron in the magma ocean stage controlled the geochemistry of the mantle and core. We have studied the partitioning behaviors of elements into the silicate melt, high pressure minerals, and metallic iron under the deep upper mantle and lower mantle conditions. We employed the multi-anvil apparatus for preparing the equilibrating samples in the ranges from 16 to 27 GPa and 1700-2400 C. Both the electron probe microanalyzer (EPMA) and the Secondary Ion Mass spectrometer (SIMS) were used for analyzing the run products. We obtained the partition coefficients of various trace elements between majorite, Mg-perovskite, and liquid, and magnesiowustite, Mg-perovskite, and metallic iron. The examples of the partition coefficients of some key elements are summarized in figures, together with the previous data. We may be able to assess the origin of the mantle abundances of the elements such as transition metals by using the partitioning data obtained above. The mantle abundances of some transition metals expected by the core-mantle equilibrium under the lower mantle conditions cannot explain the observed abundance of some elements such as Mn and Ge in the mantle. Estimations of the densities of the ultrabasic magma Mg-perovskite at high pressure suggest existence of a density crossover in the deep lower mantle; flotation of Mg-perovskite occurs in the deep magma ocean under the lower mantle conditions. The observed depletion of some transition metals such as V, Cr, Mn, Fe, Co, and Ni in the mantle may be explained by the two stage process, the core-mantle equilibrium under the lower mantle conditions in the first stage, and subsequent downwards separation of the ultrabasic liquid (and magnesiowustite) and flotation of Mg-perovskite in the lower mantle.

Evolution of the Moon's Mantle and Crust as Reflected in Trace-Element Microbeam Studies of Lunar Magmatism

NASA Astrophysics Data System (ADS)

Shearer, C. K.; Floss, C.

Ion microprobe trace-element studies of lunar cumulates [ferroan anorthosites (FAN), highlands Mg suite (HMS), and highlands alkali suite (HAS)] and volcanic glasses have provided an additional perspective in reconstructing lunar magmatism and early differentiation. Calculated melt compositions for the FANs indicate that a simple lunar magma ocean (LMO) model does not account for differences between FANs with highly magnesian mafic minerals and “typical” ferroan anorthosites. The HMS and HAS appear to have crystallized from magmas that had incompatible trace-element concentrations equal to or greater than KREEP. Partial melting of distinct, hybridized sources is consistent with these calculated melt compositions. However, the high-Mg silicates with relatively low Ni content that are observed in the HMS are suggestive of other possible processes (reduction, metal removal). The compositions of the picritic glasses indicate that they were produced by melting of hybrid cumulate sources produced by mixing of early and late LMO cumulates. The wide compositional range of near-primitive mare basalts indicates small degrees of localized melting preserved the signature of distinct mantle reservoirs. The relationship between ilmenite anomalies and 182W in the mare basalts suggests that the LMO crystallized over a short period of time.

Trace element and Sr-Nd-Pb isotope geochemistry of Rungwe Volcanic Province, Tanzania: Implications for a superplume source for East Africa Rift magmatism

NASA Astrophysics Data System (ADS)

Castillo, Paterno; Hilton, David; Halldórsson, Sæmundur

2014-09-01

The recently discovered high, plume-like 3He/4He ratios at Rungwe Volcanic Province (RVP) in southern Tanzania, similar to those at the Main Ethiopian Rift in Ethiopia, strongly suggest that magmatism associated with continental rifting along the entire East African Rift System (EARS) has a deep mantle contribution (Hilton et al., 2011). New trace element and Sr-Nd-Pb isotopic data for high 3He/4He lavas and tephras from RVP can be explained by binary mixing relationships involving Early Proterozoic (+/- Archaean) lithospheric mantle, present beneath the southern EARS, and a volatile-rich carbonatitic plume with a limited range of compositions and best represented by recent Nyiragongo lavas from the Virunga Volcanic Province also in the Western Rift. Other lavas from the Western Rift and from the southern Kenya Rift can also be explained through mixing between the same endmember components. In contrast, lavas from the northern Kenya and Main Ethiopian rifts can be explained through variable mixing between the same mantle plume material and the Middle to Late Proterozoic lithospheric mantle, present beneath the northern EARS. Thus, we propose that the bulk of EARS magmatism is sourced from mixing among three endmember sources: Early Proterozoic (+/- Archaean) lithospheric mantle, Middle to Late Proterozoic lithospheric mantle and a volatile-rich carbonatitic plume with a limited range of compositions. We propose further that the African Superplume, a large, seismically anomalous feature originating in the lower mantle beneath southern Africa, influences magmatism throughout eastern Africa with magmatism at RVP and Main Ethiopian Rift representing two different heads of a single mantle plume source. This is consistent with a single mantle plume origin of the coupled He-Ne isotopic signatures of mantle-derived xenoliths and/or lavas from all segments of the EARS (Halldorsson et al., 2014).

Tracing halogen and B cycling in subduction zones based on obducted, subducted and forearc serpentinites of the Dominican Republic.

PubMed

Pagé, Lilianne; Hattori, Keiko

2017-12-19

Serpentinites are important reservoirs of fluid-mobile elements in subduction zones, contributing to volatiles in arc magmas and their transport into the Earth's mantle. This paper reports halogen (F, Cl, Br, I) and B abundances of serpentinites from the Dominican Republic, including obducted and subducted abyssal serpentinites and forearc mantle serpentinites. Abyssal serpentinite compositions indicate the incorporation of these elements from seawater and sediments during serpentinization on the seafloor and at slab bending. During their subduction and subsequent lizardite-antigorite transition, F and B are retained in serpentinites, whilst Cl, Br and I are expelled. Forearc mantle serpentinite compositions suggest their hydration by fluids released from subducting altered oceanic crust and abyssal serpentinites, with only minor sediment contribution. This finding is consistent with the minimal subduction of sediments in the Dominican Republic. Forearc mantle serpentinites have F/Cl and B/Cl ratios similar to arc magmas, suggesting the importance of serpentinite dehydration in the generation of arc magmatism in the mantle wedge.

Partitioning experiments in the laser-heated diamond anvil cell: volatile content in the Earth's core.

PubMed

Jephcoat, Andrew P; Bouhifd, M Ali; Porcelli, Don

2008-11-28

The present state of the Earth evolved from energetic events that were determined early in the history of the Solar System. A key process in reconciling this state and the observable mantle composition with models of the original formation relies on understanding the planetary processing that has taken place over the past 4.5Ga. Planetary size plays a key role and ultimately determines the pressure and temperature conditions at which the materials of the early solar nebular segregated. We summarize recent developments with the laser-heated diamond anvil cell that have made possible extension of the conventional pressure limit for partitioning experiments as well as the study of volatile trace elements. In particular, we discuss liquid-liquid, metal-silicate (M-Sil) partitioning results for several elements in a synthetic chondritic mixture, spanning a wide range of atomic number-helium to iodine. We examine the role of the core as a possible host of both siderophile and trace elements and the implications that early segregation processes at deep magma ocean conditions have for current mantle signatures, both compositional and isotopic. The results provide some of the first experimental evidence that the core is the obvious replacement for the long-sought, deep mantle reservoir. If so, they also indicate the need to understand the detailed nature and scale of core-mantle exchange processes, from atomic to macroscopic, throughout the age of the Earth to the present day.

Trace Element Partitioning Between low-Ca Pyroxene and Ultracalcic Liquids.

NASA Astrophysics Data System (ADS)

Pertermann, M.; Schmidt, M. W.; Pettke, T.

2003-12-01

Low-Ca pyroxene or pigeonite ( ˜0.25-0.35 Ca per formula unit, pfu) is an important residual phase during high temperature melting of refractory mantle (e.g., ankaramite formation). High-Ca cpx (>0.6-0.7 Ca pfu) may be residual to relatively low temperature melting of fertile mantle (MOR and OI), but the opx-cpx solvus narrows considerably at higher temperatures (>1330-1350° C), leading to coexisting opx and low-Ca cpx. Little is known about the trace element partitioning of such low-Ca cpx at upper mantle conditions. Our new partitioning experiments investigate the role of low-Ca cpx during melting of depleted peridotite. Nominally anhydrous experiments with graphite-lined Pt-capsules were conducted at 1.4 GPa and 1360-1370° C. The synthetic starting material is close in composition to an ultracalcic liquid saturated in opx+pigeonite+olivine+spinel. The experiments yielded assemblages of glass, low-Ca cpx, ol, and minor Cr-spinel; opx is absent. The low-Ca clinopyroxenes have 0.20 and 0.32 Ca pfu at 1370 and 1360° C, respectively, and tetrahedral Al of 0.046 and 0.067 pfu. The liquids have ˜50 wt% SiO2, ˜12.5 wt% CaO and CaO/Al2O3 of 1.44-1.54. Pyroxenes and glasses were analyzed for trace elements (La, Ce, Nd, Sm, Eu, Gd, Dy, Er Yb, Lu, Sc, Y, Sr, Zr, Hf, V, Cr, Mn, Co, Zn) by LA-ICP-MS using a 193 nm ArF excimer laser coupled to an Elan 6100 mass spectrometer. Ablation occurred in He, and ablation spot sizes were 15-30 μ m for minerals and 50 μ m for glasses. Trace element concentrations in pyroxenes were low for most 3+ and 4+ cations. This resulted in small mineral/melt partition coefficients (D-values), approximately an order of magnitude lower than those for high-Ca cpx associated with peridotite melting, thus making the low-Ca cpx partitioning behavior rather similar to the behavior of peridotitic opx. Cpx with 0.32 Ca pfu has slightly elevated D-values for 3+ cations when compared to the 0.20 Ca pfu cpx: DSc = 0.45, DY = 0.11, DSm = 0.054 and DYb = 0.141, compared to values of 0.32, 0.065, 0.016 and 0.075, respectively. Regardless of Ca content, V, Mn, Co and Zn are mildly incompatible (Ds ˜0.5-0.9). Therefore, only Sc, V, Cr, Mn, Co, Ni and Zn are retained during partial mantle melting with a pigeonite+opx+ol residue. Most other elements partition strongly into the melt, and barring exotic residual minerals, the composition of ultracalcic liquids reflects the incompatible trace element budget of the depleted peridotite source.

Lu-Hf, in-situ Sr and Pb isotope and trace element systematics for mantle eclogites from the Diavik diamond mine: Evidence for Paleoproterozoic subduction beneath the Slave craton, Canada

NASA Astrophysics Data System (ADS)

Schmidberger, Stefanie S.; Simonetti, Antonio; Heaman, Larry M.; Creaser, Robert A.; Whiteford, Sean

2007-02-01

Lu-Hf, Sm-Nd and in-situ clinopyroxene Sr and Pb isotope systematics, and mineral major and in-situ trace element compositions were obtained for a suite of non-diamond and diamond-bearing eclogites from the Diavik kimberlites (A154; 55 Ma old), Slave craton (Canada). Temperature estimates of last equilibration in the lithosphere for the non-diamond-bearing Diavik eclogites define two groups; low-temperature (800-1050 °C) and high-temperature eclogites (1100-1300 °C). Most diamond-eclogites indicate temperatures similar to those of the high-temperature eclogites. Isotopic and major and trace element systematics for the non-diamond- and diamond-bearing eclogites indicate overlapping chemical compositions suggesting similar rock formational histories. Calculated whole rock major and trace element abundances using chemical and modal abundances for constituent minerals exhibit broad similarities with mafic cumulates from ophiolite sequences. Most importantly the calculated whole rock eclogite compositions display positive Sr and Eu anomalies, typically interpreted as the result of plagioclase accumulation in cumulate rocks of oceanic crust sequences. Initial whole rock Hf isotopic values and in-situ Sr isotope data from clinopyroxene grains provide evidence that the eclogites were derived from precursor rocks with depleted mantle isotope characteristics. These combined results support the interpretation that the eclogites from Diavik represent remnants of subducted oceanic crust. Lu-Hf isotope systematics indicate that the oceanic protolith for the eclogites formed in the Paleoproterozoic at ˜ 2.1 Ga, which is in agreement with the in-situ Pb isotope data from clinopyroxene. This result also corroborates the ˜ 2.1 Ga Lu-Hf model ages recorded by mantle zircons from eclogite found within the Jericho kimberlite in the northern Slave Province (˜ 200 km northwest of Diavik). The results from both studies indicate a link between eclogite formation and Paleoproterozoic subduction of oceanic lithosphere along the present-day western margin of the Archean Slave craton.

Mantle heterogeneity and crustal recycling in Archean granite-greenstone belts - Evidence from Nd isotopes and trace elements in the Rainy Lake area, Superior Province, Ontario, Canada

NASA Technical Reports Server (NTRS)

Shirey, Steven B.; Hanson, Gilbert N.

1986-01-01

Crustal evolution in the Rainy Lake area, Ontario is studied in terms of geochemical characteristics. The Nd isotope data are examined for heterogeneity of the Archean mantle, and the Sm/Nd depletion of the mantle is analyzed. The Nd isotope systematics of individual rock suites is investigated in order to understand the difference between crust and mantle sources; the precursors and petrogenetic processes are discussed. The correlation between SiO2 content and Nd values is considered. Rapid recycling of crustal components, which were previously derived from depleted mantle sources, is suggested based on the similarity of the initial Nd isotopic composition for both mantle-derived and crustally-derived rocks.

New Martian Meteorite Is One of the Most Oxidized Found to Date

NASA Technical Reports Server (NTRS)

Hui, Hejiu; Peslier, Anne; Lapen, Thomas J.; Shafer, John T.; Brandon, Alan D.; Irving, Anthony J.

2014-01-01

As of 2013, about 60 meteorites from the planet Mars have been found and are being studied. Each time a new Martian meteorite is found, a wealth of new information comes forward about the red planet. The most abundant type of Martian meteorite is a shergottite; its lithologies are broadly similar to those of Earth basalts and gabbros; i.e., crustal igneous rocks. The entire suite of shergottites is characterized by a range of trace element, isotopic ratio, and oxygen fugacity values that mainly reflect compositional variations of the Martian mantle from which these magmas came. A newly found shergottite, NWA 5298, was the focus of a study performed by scientists within the Astromaterials Research and Exploration Science (ARES) Directorate at the Johnson Space Center (JSC) in 2012. This sample was found in Morocco in 2008. Major element analyses were performed in the electron microprobe (EMP) laboratory of ARES at JSC, while the trace elements were measured at the University of Houston by laser inductively coupled plasma mass spectrometry (ICPMS). A detailed analysis of this stone revealed that this meteorite is a crystallized magma that comes from the enriched end of the shergottite spectrum; i.e., trace element enriched and oxidized. Its oxidation comes in part from its mantle source and from oxidation during the magma ascent. It represents a pristine magma that did not mix with any other magma or see crystal accumulation or crustal contamination on its way up to the Martian surface. NWA 5298 is therefore a direct, albeit evolved, melt from the Martian mantle and, for its lithology (basaltic shergottite), it represents the oxidized end of the shergottite suite. It is thus a unique sample that has provided an end-member composition for Martian magmas.

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.

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.

Effect of Mantle Wedge Hybridization by Sediment Melt on Geochemistry of Arc Magma and Arc Mantle Source - Insights from Laboratory Experiments at High Pressures and Temperatures

NASA Astrophysics Data System (ADS)

Mallik, A.; Dasgupta, R.; Tsuno, K.; Nelson, J. M.

2015-12-01

Generation of arc magmas involves metasomatism of the mantle wedge by slab-derived H2O-rich fluids and/or melts and subsequent melting of the modified source. The chemistry of arc magmas and the residual mantle wedge are not only regulated by the chemistry of the slab input, but also by the phase relations of metasomatism or hybridization process in the wedge. The sediment-derived silica-rich fluids and hydrous partial melts create orthopyroxene-rich zones in the mantle wedge, due to reaction of mantle olivine with silica in the fluid/melt [1,2]. Geochemical evidence for such a reaction comes from pyroxenitic lithologies coexisting with peridotite in supra-subduction zones. In this study, we have simulated the partial melting of a parcel of mantle wedge modified by bulk addition of sediment-derived melt with variable H2O contents to investigate the major and trace element chemistry of the magmas and the residues formed by this process. Experiments at 2-3 GPa and 1150-1300 °C were conducted on mixtures of 25% sediment-derived melt and 75% lherzolite, with bulk H2O contents varying from 2 to 6 wt.%. Partial reactive crystallization of the rhyolitic slab-derived melt and partial melting of the mixed source produced a range of melt compositions from ultra-K basanites to basaltic andesites, in equilibrium with an orthopyroxene ± phlogopite ± clinopyroxene ± garnet bearing residue, depending on P and bulk H2O content. Model calculations using partition coefficients (from literature) of trace elements between experimental minerals and silicate melt suggest that the geochemical signatures of the slab-derived melt, such as low Ce/Pb and depletion in Nb and Ta (characteristic slab signatures) are not erased from the resulting melt owing to reactive crystallization. The residual mineral assemblage is also found to be similar to the supra-subduction zone lithologies, such as those found in Dabie Shan (China) and Sanbagawa Belt (Japan). In this presentation, we will also compare the major and trace element characteristics of bulk rock and minerals found in orthopyroxenites from supra-subduction zones with the residua formed in our experiments, to differentiate between melt versus fluid, and sediment- versus basalt-derived flux in the mantle wedge. [1] Mallik et al. (2015) CMP169(5) [2] Sekine & Wyllie (1982) CMP 81(3)

Core-Mantle Partitioning of Volatile Siderophile Elements and the Origin of Volatile Elements in the Earth

NASA Technical Reports Server (NTRS)

Nickodem, K.; Righter, K.; Danielson, L.; Pando, K.; Lee, C.

2012-01-01

There are currently several hypotheses on the origin of volatile siderophile elements in the Earth. One hypothesis is that they were added during Earth s accretion and core formation and mobilized into the metallic core [1], others claim multiple stage origin [2], while some hypothesize that volatiles were added after the core already formed [3]. Several volatile siderophile elements are depleted in Earth s mantle relative to the chondrites, something which continues to puzzle many scientists. This depletion is likely due to a combination of volatility and core formation. The Earth s core is composed of Fe and some lighter constituents, although the abundances of these lighter elements are unknown [4]. Si is one of these potential light elements [5] although few studies have analyzed the effect of Si on metal-silicate partitioning, in particular the volatile elements. As, In, Ge, and Sb are trace volatile siderophile elements which are depleted in the mantle but have yet to be extensively studied. The metal-silicate partition coefficients of these elements will be measured to determine the effect of Si. Partition coefficients depend on temperature, pressure, oxygen fugacity, and metal and silicate composition and can constrain the concentrations of volatile, siderophile elements found in the mantle. Reported here are the results from 13 experiments examining the partitioning of As, In, Ge, and Sb between metallic and silicate liquid. These experiments will examine the effect of temperature, and metal-composition (i.e., Si content) on these elements in or-der to gain a greater understanding of the core-mantle separation which occurred during the Earth s early stages. The data can then be applied to the origin of volatile elements in the Earth.

Perovskite in Earth’s deep interior

NASA Astrophysics Data System (ADS)

Hirose, Kei; Sinmyo, Ryosuke; Hernlund, John

2017-11-01

Silicate perovskite-type phases are the most abundant constituent inside our planet and are the predominant minerals in Earth’s lower mantle more than 660 kilometers below the surface. Magnesium-rich perovskite is a major lower mantle phase and undergoes a phase transition to post-perovskite near the bottom of the mantle. Calcium-rich perovskite is proportionally minor but may host numerous trace elements that record chemical differentiation events. The properties of mantle perovskites are the key to understanding the dynamic evolution of Earth, as they strongly influence the transport properties of lower mantle rocks. Perovskites are expected to be an important constituent of rocky planets larger than Mars and thus play a major role in modulating the evolution of terrestrial planets throughout the universe.

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.

Meter Scale Heterogeneities in the Oceanic Mantle Revealed in Ophiolites Peridotites

NASA Astrophysics Data System (ADS)

Haller, M. B.; Walker, R. J.; Day, J. M.; O'Driscoll, B.; Daly, J. S.

2016-12-01

Mid-ocean ridge basalts and other oceanic mantle-derived rocks do not capture the depleted endmember isotopic compositions present in oceanic peridotites. Ophiolites are especially useful in interrogating this issue as field-based observations can be paired with geochemical investigations over a wide range of geologic time. Grid sampling methods (3m x 3m) at the 497 Ma Leka Ophiolite Complex (LOC), Norway, and the 1.95 Ga Jormua Ophiolite Complex (JOC), Finland, offer an opportunity to study mantle domains at the meter and kilometer scale, and over a one billion year timespan. The lithology of each locality predominately comprises harzburgite, hosting layers and lenses of dunite and pyroxenite. Here, we combine highly siderophile elements (HSE) and Re-Os isotopic analysis of these rocks with major and trace element measurements. Harzburgites at individual LOC grid sites show variations in γOs(497 Ma) (-2.1 to +2.2) at the meter scale. Analyses of adjacent, more radiogenic dunites within the same LOC grid, reveal that dunites may either have similar γOs to their host harzburgite, or different, implying interactions between spatially associated rock types may differ at the meter scale. Averaged γOs values between the mantle sections of two LOC grid sites (+1.3 and -0.4) separated by 5 km indicate km-scale heterogeneity in the convecting upper mantle. Pd/Ir and Ru/Ir ratios are scattered and do not obviously correlate with γOs values. Analyses of pyroxenites within LOC grid sections, thin section observations of relict olivine grains, and whole rock major and trace element data are also examined to shed light on the causes of the isotopic heterogeneities in the LOC. Data from JOC grid sampling will be presented as well.

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.

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.

Plate tectonics and continental basaltic geochemistry throughout Earth history

NASA Astrophysics Data System (ADS)

Keller, Brenhin; Schoene, Blair

2018-01-01

Basaltic magmas constitute the primary mass flux from Earth's mantle to its crust, carrying information about the conditions of mantle melting through which they were generated. As such, changes in the average basaltic geochemistry through time reflect changes in underlying parameters such as mantle potential temperature and the geodynamic setting of mantle melting. However, sampling bias, preservation bias, and geological heterogeneity complicate the calculation of representative average compositions. Here we use weighted bootstrap resampling to minimize sampling bias over the heterogeneous rock record and obtain maximally representative average basaltic compositions through time. Over the approximately 4 Ga of the continental rock record, the average composition of preserved continental basalts has evolved along a generally continuous trajectory, with decreasing compatible element concentrations and increasing incompatible element concentrations, punctuated by a comparatively rapid transition in some variables such as La/Yb ratios and Zr, Nb, and Ti abundances approximately 2.5 Ga ago. Geochemical modeling of mantle melting systematics and trace element partitioning suggests that these observations can be explained by discontinuous changes in the mineralogy of mantle partial melting driven by a gradual decrease in mantle potential temperature, without appealing to any change in tectonic process. This interpretation is supported by the geochemical record of slab fluid input to continental basalts, which indicates no long-term change in the global proportion of arc versus non-arc basaltic magmatism at any time in the preserved rock record.

Rethinking geochemical feature of the Afar and Kenya mantle plumes and geodynamic implications

NASA Astrophysics Data System (ADS)

Meshesha, Daniel; Shinjo, Ryuichi

2008-09-01

We discuss the spatial and temporal variation in the geochemistry of mantle sources which were sampled by the Eocene to Quaternary mafic magmas in the vicinity of the Afar and Kenya plume upwelling zones, East Africa. Despite the contributions of lithospheric and crustal sources, carefully screened Eocene to Quaternary mafic lavas display wide range of Sr-Nd-Pb isotopic and incompatible trace elemental compositions that can be attributed to significant intraplume heterogeneity. The geochemical variations reflect the involvement of at least four mantle plume components as sources for the northeastern Africa magmatism: (1) isotopically depleted but trace element-enriched component; (2) component characterized by radiogenic Pb isotope signatures (HIMU?); (3) enriched mantle-like component; and (4) high-3He/4He-type (as HT2-type basalts) plume component. The first component disappears in the Miocene-Quaternary magmatism, and the second component is hardly recognized after the eruption of Miocene basalt in southern Ethiopia. Plume-unrelated depleted asthenosphere starts to involve at a nascent stage of seafloor spreading centers in the Red Sea and Gulf of Aden. The other two-plume components have persisted from the late Eocene to present, but their proportions have changed through time and space. We propose a model of multiple impingements of plumelets within the broad upwelling zone connected to the African Superplume in the lower mantle beneath southern Africa. The plumelet contains a matrix of high-3He/4He-type component with blobs, streaks, or ribbons of other components.

Rapid Mantle Source Variations During the Latest Episode of Kilauea's Prolonged Pu'u O'o Eruption, Hawaii

NASA Astrophysics Data System (ADS)

Marske, J. P.; Garcia, M. O.; Pietruszka, A. J.; Norman, M. D.; Rhodes, J. M.

2006-12-01

Nearly 24 years of continuous geochemical monitoring of lavas from the current Pu'u O'o eruption allow us to probe the mantle processes beneath Kilauea Volcano in unparalleled detail. Here we present new measurements Pb, Sr, and Nd isotope ratios and major- and trace-element abundances for lavas from episode 55 (1997-2006), which marks the longest and most voluminous interval of this eruption. Pu'u O'o lavas erupted since 1985 display systematic decreases in their TiO2, K2O, P2O5 and CaO abundances (normalized to 10 wt. % MgO to correct for olivine control) due to changes in the parental magma composition. Incompatible element ratios (e.g., Ba/Nb and La/Y) also show overall temporal decreases. Earlier erupted Pu'u O'o lavas displayed the most significant decrease in incompatible element ratios with near constant SiO2 contents, and a gradual increase in 87Sr/86Sr ratios. However, episode 55 lavas record significant increases in MgO- normalized SiO2 contents and 87Sr/86Sr with nearly constant (e.g. Ba/Nb) or a slightly reversed (e.g., TiO2 and K2O) trends in incompatible element ratios and abundances. There is little variation of 206Pb/204Pb ratios in lavas (18.38-18.43) erupted since 1985. Neither a single mantle source composition nor a change in partial melting conditions alone can explain these observations. Based on the isotopic and chemical variability, we conclude that early Pu'u O'o lavas originated from two distinct mantle source components: (1) a long-term depleted component (with relatively low 87Sr/86Sr ratios) that originated within the deep source of the Hawaiian plume that characterizes the earlier part of the eruption (1985-1992), and (2) a recently depleted component (i.e. a component that was recently depleted by prior melting) with low abundances of incompatible elements became increasingly important from 1992-1997. More recently, Pu'u O'o has tapped greater proportions of a new (3) long-term less depleted component (with higher 87Sr/86Sr ratios than observed from 1985-1992) that originated within the deep source region of the plume. This third component lies within typical Pb, Sr and Nd isotopic space for Kilauea, but represents a new source composition for the Pu'u O'o eruption. The systematic geochemical evolution of Pu'u O'o lavas reflects changes in the proportions of the mantle source components tapped throughout the eruption. The rapid isotope variations (on a time scale of years) in the most recent lavas suggest the mantle source components are heterogeneous on an extremely small scale, relative to the size of Kilauea's melting region.

Transfer of subduction fluids into the deforming mantle wedge during nascent subduction: Evidence from trace elements and boron isotopes (Semail ophiolite, Oman)

NASA Astrophysics Data System (ADS)

Prigent, C.; Guillot, S.; Agard, P.; Lemarchand, D.; Soret, M.; Ulrich, M.

2018-02-01

The basal part of the Semail ophiolitic mantle was (de)formed at relatively low temperature (LT) directly above the plate interface during "nascent subduction" (the prelude to ophiolite obduction). This subduction-related LT deformation was associated with progressive strain localization and cooling, resulting in the formation of porphyroclastic to ultramylonitic shear zones prior to serpentinization. Using petrological and geochemical analyses (trace elements and B isotopes), we show that these basal peridotites interacted with hydrous fluids percolating by porous flow during mylonitic deformation (from ∼850 down to 650 °C). This process resulted in 1) high-T amphibole crystallization, 2) striking enrichments of minerals in fluid mobile elements (FME; particularly B, Li and Cs with concentrations up to 400 times those of the depleted mantle) and 3) peridotites with an elevated δ11B of up to +25‰. These features indicate that the metasomatic hydrous fluids are most likely derived from the dehydration of subducting crustal amphibolitic materials (i.e., the present-day high-T sole). The rapid decrease in metasomatized peridotite δ11B with increasing distance to the contact with the HT sole (to depleted mantle isotopic values in <1 km) suggests an intense interaction between peridotites and rapid migrating fluids (∼1-25 m.y-1), erasing the initial high-δ11B subduction fluid signature within a short distance. The increase of peridotite δ11B with increasing deformation furthermore indicates that the flow of subduction fluids was progressively channelized in actively deforming shear zones parallel to the contact. Taken together, these results also suggest that the migration of subduction fluids/melts by porous flow through the subsolidus mantle wedge (i.e., above the plate interface at sub-arc depths) is unlikely to be an effective mechanism to transport slab-derived elements to the locus of partial melting in subduction zones.

Melt extraction and mantle source at a Southwest Indian Ridge Dragon Bone amagmatic segment on the Marion Rise

NASA Astrophysics Data System (ADS)

Gao, Changgui; Dick, Henry J. B.; Liu, Yang; Zhou, Huaiyang

2016-03-01

This paper works on the trace and major element compositions of spatially associated basalts and peridotites from the Dragon Bone amagmatic ridge segment at the eastern flank of the Marion Platform on the ultraslow spreading Southwest Indian Ridge. The rare earth element compositions of basalts do not match the pre-alteration Dragon Bone peridotite compositions, but can be modeled by about 5 to 10% non-modal batch equilibrium melting from a DMM source. The Dragon Bone peridotites are clinopyroxene-poor harzburgite with average spinel Cr# 27.7. The spinel Cr# indicates a moderate degree of melting. However, CaO and Al2O3 of the peridotites are lower than other abyssal peridotites at the same Mg# and extent of melting. This requires a pyroxene-poor initial mantle source composition compared to either hypothetical primitive upper mantle or depleted MORB mantle sources. We suggest a hydrous melting of the initial Dragon Bone mantle source, as wet melting depletes pyroxene faster than dry. According to the rare earth element patterns, the Dragon Bone peridotites are divided into two groups. Heavy REE in Group 1 are extremely fractionated from middle REE, which can be modeled by 7% fractional melting in the garnet stability field and another 12.5 to 13.5% in the spinel stability field from depleted and primitive upper mantle sources, respectively. Heavy REE in Group 2 are slightly fractionated from middle REE, which can be modeled by 15 to 20% fractional melting in the spinel stability field from a depleted mantle source. Both groups show similar melting degree to other abyssal peridotites. If all the melt extraction occurred at the middle oceanic ridge where the peridotites were dredged, a normal 6 km thick oceanic crust is expected at the Dragon Bone segment. However, the Dragon Bone peridotites are exposed in an amagmatic ridge segment where only scattered pillow basalts lie on a partially serpentinized mantle pavement. Thus their depletion requires an earlier melting occurred at other place. Considering the hydrous melting of the initial Dragon Bone mantle source, we suggest the earlier melting event occurred in an arc terrain, prior to or during the closure of the Mozambique Ocean in the Neproterozoic, and the subsequent assembly of Gondwana. Then, the Al2O3 depleted and thus buoyant peridotites became the MORB source for Southwest Indian Ridge and formed the Marion Rise during the Gondwana breakup.

Geochemical Evidence for a Terrestrial Magma Ocean

NASA Technical Reports Server (NTRS)

Agee, Carl B.

1999-01-01

The aftermath of phase separation and crystal-liquid fractionation in a magma ocean should leave a planet geochemically differentiated. Subsequent convective and other mixing processes may operate over time to obscure geochemical evidence of magma ocean differentiation. On the other hand, core formation is probably the most permanent, irreversible part of planetary differentiation. Hence the geochemical traces of core separation should be the most distinct remnants left behind in the mantle and crust, In the case of the Earth, core formation apparently coincided with a magma ocean that extended to a depth of approximately 1000 km. Evidence for this is found in high pressure element partitioning behavior of Ni and Co between liquid silicate and liquid iron alloy, and with the Ni-Co ratio and the abundance of Ni and Co in the Earth's upper mantle. A terrestrial magma ocean with a depth of 1000 km will solidify from the bottom up and first crystallize in the perovskite stability field. The largest effect of perovskite fractionation on major element distribution is to decrease the Si-Mg ratio in the silicate liquid and increase the Si-Mg ratio in the crystalline cumulate. Therefore, if a magma ocean with perovskite fractionation existed, then one could expect to observe an upper mantle with a lower than chondritic Si-Mg ratio. This is indeed observed in modern upper mantle peridotites. Although more experimental work is needed to fully understand the high-pressure behavior of trace element partitioning, it is likely that Hf is more compatible than Lu in perovskite-silicate liquid pairs. Thus, perovskite fractionation produces a molten mantle with a higher than chondritic Lu-Hf ratio. Arndt and Blichert-Toft measured Hf isotope compositions of Barberton komatiites that seem to require a source region with a long-lived, high Lu-Hf ratio. It is plausible that that these Barberton komatiites were generated within the majorite stability field by remelting a perovskite-depleted part of the upper mantle transition zone.

Trace-element patterns of fibrous and monocrystalline diamonds: Insights into mantle fluids

NASA Astrophysics Data System (ADS)

Rege, S.; Griffin, W. L.; Pearson, N. J.; Araujo, D.; Zedgenizov, D.; O'Reilly, S. Y.

2010-08-01

During their growth diamonds may trap micron-scale inclusions of the fluids from which they grew, and these "time capsules" provide insights into the metasomatic processes that have modified the subcontinental lithospheric mantle. LAM-ICPMS analysis of trace elements in > 500 fibrous and monocrystalline diamonds worldwide has been used to understand the nature of these fluids. Analyses of fibrous diamonds define two general types of pattern, a "fibrous-high" (FH) one with high contents of LREE, Ba and K, and a "fibrous-low" (FL) pattern characterized by depletion in LREE/MREE, Ba and K, negative anomalies in Sr and Y, and subchondritic Zr/Hf and Nb/Ta. Both types may be found in fibrous diamonds from single deposits, and in three Yakutian pipes some diamonds show abrupt transitions from inclusion-rich cores with FH patterns to clearer rims with FL patterns. Most monocrystalline diamonds show FL-type patterns, but some have patterns that resemble those of FH fibrous diamonds. Peridotitic and eclogitic monocrystalline diamonds may show either patterns with relatively flat REE, or patterns with more strongly depleted LREE. Kimberlites that contain peridotitic diamonds with "high" patterns also contain eclogitic diamonds with "high" patterns. Strong similarities in the patterns of these two groups of diamonds may suggest high fluid/rock ratios. Many diamonds of the "superdeep" paragenesis have trace-element patterns similar to those of other monocrystalline diamonds. This may be evidence that the trace-element compositions of deep-seated fluids are generally similar to those that form diamonds in the subcontinental lithospheric mantle. The element fractionations observed between the FH and FL patterns are consistent with the immiscible separation of a silicic fluid from a carbonatite-silicate fluid, leaving a residual carbonatitic fluid strongly enriched in LREE, Ba and alkalies. This model would suggest that most monocrystalline diamonds crystallized from the more silicic fraction. Comparison with studies of single fluid inclusions in fibrous diamonds suggests that the FH patterns reflect trapped inclusions of high-Mg and low-Mg carbonatitic high-density fluids. In terms of the rock-forming elements, the fluids that precipitated the rims of some fibrous diamonds (FL pattern) and most monocrystalline diamonds are broadly similar to some hydro-silicic high-density fluids found in fibrous diamonds. However, there are still significant differences between the trace-element patterns of most monocrystalline diamonds and known high-density fluids, and further research is required to understand the formation and growth of these diamonds.

Experimental Partitioning of Chalcophile Elements between Mantle Silicate Minerals and Basaltic Melt at High Pressures and Temperatures - Implications for Sulfur Geochemistry of Mantle and Crust

NASA Astrophysics Data System (ADS)

Dasgupta, R.; Jego, S.; Ding, S.; Li, Y.; Lee, C. T.

2015-12-01

The behavior of chalcophile elements during mantle melting, melt extraction, and basalt differentiation is critical for formation of ore deposits and geochemical model and evolution of crust-mantle system. While chalcophile elements are strongly partitioned into sulfides, their behavior with different extent of melting, in particular, in the absence of sulfides, can only be modeled with complete knowledge of the partitioning behavior of these elements between dominant mantle minerals and basaltic melt with or without dissolved sulfide (S2-). However, experimental data on mineral-melt partitioning are lacking for many chalcophile elements. Crystallization experiments were conducted at 3 GPa and 1450-1600 °C using a piston cylinder and synthetic silicate melt compositions similar to low-degree partial melt of peridotite. Starting silicate mixes doped with 100-300 ppm of each of various chalcophile elements were loaded into Pt/graphite double capsules. To test the effect of dissolved sulfur in silicate melt on mineral-melt partitioning of chalcophile elements, experiments were conducted on both sulfur-free and sulfur-bearing (1100-1400 ppm S in melt) systems. Experimental phases were analyzed by EPMA (for major elements and S) and LA-ICP-MS (for trace elements). All experiments produced an assemblage of cpx + melt ± garnet ± olivine ± spinel and yielded new partition coefficients (D) for Sn, Zn, Mo, Sb, Bi, Pb, and Se for cpx/melt, olivine/melt, and garnet/melt pairs. Derived Ds (mineral/basalt) reveal little effect of S2- in the melt on mineral-melt partition coefficients of the measured chalcophile elements, with Ds for Zn, Mo, Bi, Pb decreasing by less than a factor of 2 from S-free to S-bearing melt systems or remaining similar, within error, between S-free and S-bearing melt systems. By combining our data with existing partitioning data between sulfide phases and silicate melt we model the fractionation of these elements during mantle melting and basalt crystallization. The model results are compared with the chalcophile element abundance in oceanic basalts. We will discuss the implications of our new partitioning data and model results on sulfur and chalcophile element geochemistry of mantle source regions of ocean floor basalts and the fate of sulfides during mantle melting.

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.

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.

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.

Tracing iron-carbon redox from surface to core

NASA Astrophysics Data System (ADS)

McCammon, C. A.; Cerantola, V.; Bykova, E.; Kupenko, I.; Bykov, M.; Chumakov, A. I.; Rüffer, R.; Dubrovinsky, L. S.

2017-12-01

Numerous redox reactions separate the Earth's oxidised surface from its reduced core. Many involve iron, the Earth's most abundant element and the mantle's most abundant transition element. Most iron redox reactions (although not all) also involve other elements, including carbon, where iron-carbon interactions drive a number of important processes within the Earth, for example diamond formation. Many of the Earth's redox boundaries are sharp, much like the seismic properties that define them, for example between the lower mantle and the core. Other regions that appear seismically homogeneous, for example the lower mantle, harbour a wealth of reactions between oxidised and reduced phases of iron and carbon. We have undertaken many experiments at high pressure and high temperature on phases containing iron and carbon using synchrotron-based X-rays to probe structures and iron oxidation states. Results demonstrate the dominant role that crystal structures play in determining the stable oxidation states of iron and carbon, even when oxygen fugacity (and common sense) would suggest otherwise. Iron in bridgmanite, for example, occurs predominantly in its oxidised form (ferric iron) throughout the lower mantle, despite the inferred reducing conditions. Newly discovered structures of iron carbonate also stabilise ferric iron, while simultaneously reducing some carbon to diamond to balance charge. Other high-pressure iron carbonates appear to be associated with the emerging zoo of iron oxide phases, involving transitions between ferrous and ferric iron through the exchange of oxygen. The presentation will trace redox relations between iron and carbon from the Earth's surface to its core, with an emphasis on recent experimental results.

Melt migration and mantle chromatography, 2: a time-series Os isotope study of Mauna Loa volcano, Hawaii

NASA Astrophysics Data System (ADS)

Hauri, Erik H.; Kurz, Mark D.

1997-12-01

We have determined the major element, trace element, and Os isotopic compositions of a stratigraphic suite of tholeiitic basalts spanning >30,000 years of the eruptive history of Mauna Loa volcano. Good correlations are observed between Os isotopes and the isotopes of Sr, Nd, Pb and He. In addition, the isotopes correlate with fractionation-corrected major element abundances within this single volcano, and provide a record of increased melting of mafic material with time at Mauna Loa. Chromatographic element fractionation during melt transport is shown to be negligible based on the good correlations of the isotopes of the compatible element Os with the other incompatible element tracers. The temporal variation at Mauna Loa is best described by the translation of the volcano over a Hawaiian plume which is radially zoned in composition. The radial zonation is a predicted consequence of thermal entrainment during flow in a mantle plume conduit.

Models of earth structure inferred from neodymium and strontium isotopic abundances

PubMed Central

Wasserburg, G. J.; DePaolo, D. J.

1979-01-01

A simplified model of earth structure based on the Nd and Sr isotopic characteristics of oceanic and continental tholeiitic flood basalts is presented, taking into account the motion of crustal plates and a chemical balance for trace elements. The resulting structure that is inferred consists of a lower mantle that is still essentially undifferentiated, overlain by an upper mantle that is the residue of the original source from which the continents were derived. PMID:16592688

Geochemical characterization of a Quaternary monogenetic volcano in Erciyes Volcanic Complex: Cora Maar (Central Anatolian Volcanic Province, Turkey)

NASA Astrophysics Data System (ADS)

Gencalioglu-Kuscu, Gonca

2011-11-01

Central Anatolian Volcanic Province (CAVP) is a fine example of Neogene-Quaternary post-collisional volcanism in the Alpine-Mediterranean region. Volcanism in the Alpine-Mediterranean region comprises tholeiitic, transitional, calc-alkaline, and shoshonitic types with an "orogenic" fingerprint. Following the orogenic volcanism, subordinate, within-plate alkali basalts ( sl) showing little or no orogenic signature are generally reported in the region. CAVP is mainly characterized by widespread calc-alkaline andesitic-dacitic volcanism with orogenic trace element signature, reflecting enrichment of their source regions by subduction-related fluids. Cora Maar (CM) located within the Erciyes pull-apart basin, is an example to numerous Quaternary monogenetic volcanoes of the CAVP, generally considered to be alkaline. Major and trace element geochemical and geochronological data for the CM are presented in comparison with other CAVP monogenetic volcanoes. CM scoria is basaltic andesitic, transitional-calc-alkaline in nature, and characterized by negative Nb-Ta, Ba, P and Ti anomalies in mantle-normalized patterns. Unlike the "alkaline" basalts of the Mediterranean region, other late-stage basalts from the CAVP monogenetic volcanoes are classified as tholeiitic, transitional and mildly alkaline. They display the same negative anomalies and incompatible element ratios as CM samples. In this respect, CM is comparable to other CAVP monogenetic basalts ( sl), but different from the Meditterranean intraplate alkali basalts. Several lines of evidence suggest derivation of CM and other CAVP monogenetic basalts from shallow depths within the lithospheric mantle, that is from a garnet-free source. In a wider regional context, CAVP basalts ( sl) are comparable to Apuseni (Romania) and Big Pine (Western Great Basin, USA) volcanics, except the former have depleted Ba contents. This is a common feature for the CAVP volcanics and might be related to crustal contamination or source characteristics. Indeed, HFS and other incompatible element ratios suggest the role of crustal contamination in the genesis of the CAVP monogenetic basalts.

Petrological constraints on melt generation beneath the Asal Rift (Djibouti) using quaternary basalts

NASA Astrophysics Data System (ADS)

Pinzuti, Paul; Humler, Eric; Manighetti, Isabelle; Gaudemer, Yves

2013-08-01

The temporal evolution of the mantle melting processes in the Asal Rift is evaluated from the chemical composition of 56 new lava flows sampled along 10 km of the rift axis and 9 km off-axis (i.e., erupted within the last 620 kyr). Petrological and primary geochemical results show that most of the samples of the inner floor of the Asal Rift are affected by plagioclase accumulation. Trace element ratios and major element compositions corrected for mineral accumulation and crystallization show a symmetric pattern relative to the rift axis and preserved a clear signal of mantle melting depth variations. While FeO, Fe8.0, Zr/Y, and (Dy/Yb)N decrease from the rift shoulders to the rift axis, SiO2, Na/Ti, Lu/Hf increase and Na2O and Na8.0 are constant across the rift. These variations are qualitatively consistent with shallow melting beneath the rift axis and deeper melting for off-axis lava flows. Na8.0 and Fe8.0 contents show that beneath the rift axis, melting paths are shallow, from 81 ± 4 to 43 ± 5 km. These melting paths are consistent with adiabatic melting in normal-temperature fertile asthenosphere, beneath an extensively thinned mantle lithosphere. On the contrary, melting on the rift shoulders (from 107 ± 7 to 67 ± 8 km) occurred beneath thicker lithosphere, requiring a mantle solidus temperature 100 ± 40°C hotter. In this geodynamic environment, the calculated rate of lithospheric thinning appears to be 4.0 ± 2.0 cm yr-1, a value close to the mean spreading rate (2.9 ± 0.2 cm yr-1) over the last 620 kyr.

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.

Geochemistry of Volcanic Rocks from International Ocean Discovery Program (IODP) Site 1438, Amami Sankaku Basin: Implications for Izu-Bonin-Mariana (IBM) Arc Initiation

NASA Astrophysics Data System (ADS)

Hickey-Vargas, R.; Ishizuka, O.; Yogodzinski, G. M.; Bizimis, M.; Savov, I. P.; McCarthy, A. J.; Arculus, R. J.; Bogus, K.

2015-12-01

IODP Expedition 351 drilled 150 m of volcanic basement overlain by 1461 m of sedimentary material at Site 1438 in the Amami Sankaku basin, just west of the Kyushu Palau Ridge, the locus of IBM arc initiation. Age interpretations based on biostratigraphy (Arculus et al., Nat. Geosci., in-press) determined that the age of the basement section is between 64 and 51 Ma, encompassing the age of the earliest volcanic products of the IBM arc. The Site 1438 volcanic basement consists of multiple flows of aphyric microcrystalline to finely crystalline basalts containing plagioclase and clinopyroxene with rare olivine pseudomorphs. New XRF major and ICPMS trace element data confirm findings of shipboard analysis that the basalts are moderately differentiated (6-14 % MgO; Mg# = 51-83; 73-490 ppm Cr and 58-350 ppm Ni) with downcore variations related to flow units. Ti/V and Ti/Sc ratios are 16-27 and 75-152, respectively, with lowest values at the base of the core. One prominent characteristic of the basalts is their depletion of immobile highly incompatible elements compared with MORB. Basalts have MORB-normalized La/Nd of 0.5 to 0.9, and most have Th/La < 0.05. Although all basalts are LREE-depleted, La/Nd ratios increase slightly upcore, and Th enrichment compared with LREE occurs in the uppermost 5 meters. Cs, Rb, K, Ba and U are concomitantly enriched relative to LREE in several intervals as a probable result of seawater alteration, but ratios less than those of MORB are found in other areas. In contrast to basement, andesites from three sills in the lowermost sedimentary unit have arc-like trace element patterns with La/Nb > 3 and primitive mantle normalized La/Yb > 1. Our results suggest that mantle melting at the onset of subduction involved exceptionally depleted sources. Enrichment over time may be related to increasing subduction inputs and/or other processes, such as entrainment of fertile asthenosphere during extension of the overriding plate.

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.

Insights into mantle heterogeneities: mid-ocean ridge basalt tapping an ocean island magma source in the North Fiji Basin

NASA Astrophysics Data System (ADS)

Brens, R., Jr.; Jenner, F. E.; Bullock, E. S.; Hauri, E. H.; Turner, S.; Rushmer, T. A.

2015-12-01

The North Fiji Basin (NFB), and connected Lau Basin, is located in a complex area of volcanism. The NFB is a back-arc basin (BAB) that is a result of an extinct subduction zone, incorporating the complicated geodynamics of two rotating landmasses: Fiji and the Vanuatu island arc. Collectively this makes the spreading centers of the NFB the highest producing spreading centers recorded. Here we present volatile concentrations, major, and trace element data for a previously undiscovered triple junction spreading center in the NFB. We show our enrichment samples contain some of the highest water contents yet reported from (MORB). The samples from the NFB exhibit a combination of MORB-like major chemical signatures along with high water content similar to ocean island basalts (OIB). This peculiarity in geochemistry is unlike other studied MORB or back-arc basin (to our knowledge) that is not attributed to subduction related signatures. Our results employ the use of volatiles (carbon dioxide and water) and their constraints (Nb and Ce) combined with trace element ratios to indicate a potential source for the enrichment in the North Fiji Basin. The North Fiji Basin lavas are tholeiitic with similar major element composition as averaged primitive normal MORB; with the exception of averaged K2O and P2O5, which are still within range for observed normal MORB. For a mid-ocean ridge basalt, the lavas in the NFB exhibit a large range in volatiles: H2O (0.16-0.9 wt%) and CO2 (80-359 ppm). The NFB lavas have volatile levels that exceed the range of MORB and trend toward a more enriched source. In addition, when compared to MORB, the NFB lavas are all enriched in H2O/Ce. La/Sm values in the NFB lavas range from 0.9 to 3.8 while, Gd/Yb values range from 1.2 to 2.5. The NFB lavas overlap the MORB range for both La/Sm (~1.1) and Gd/Yb (~1.3). However, they span a larger range outside of the MORB array. High La/Sm and Gd/Yb ratios (>1) are indications of deeper melting within the stability field of garnet and/or spinel lherzolite, suggesting that the source of these lavas may stem from MORB mixing with an enriched plume (OIB) source. The discovery of these magmatic signatures beneath the North Fiji Basin is important in understanding the heterogeneities of volatiles in the mantle, in addition to linking deeper mantle and subsurface crustal processes.

Multiple enrichment of the Carpathian-Pannonian mantle: Pb-Sr-Nd isotope and trace element constraints

NASA Astrophysics Data System (ADS)

Rosenbaum, Jeffrey M.; Wilson, Marjorie; Downes, Hilary

1997-07-01

Pb isotope compositions of acid-leached clinopyroxene and amphibole mineral separates from spinel peridotite mantle xenoliths entrained in Tertiary-Quaternary alkali basalts from the Carpathian-Pannonian Region of eastern Europe provide important constraints on the processes of metasomatic enrichment of the mantle lithosphere in an extensional tectonic setting associated with recent subduction. Principal component analysis of Pb-Sr-Nd isotope and rare earth element compositions of the pyroxenes is used to identify the geochemical characteristics of the original lithospheric mantle protolith and a spectrum of infiltrating metasomatic agents including subduction-related aqueous fluids and silicate melts derived from a subduction-modified mantle wedge which contains a St. Helena-type (HIMU) plume component. The mantle protolith is highly depleted relative to mid-ocean ridge basalt-source mantle with Pb-Nd-Sr isotope compositions consistent with an ancient depletion event. Silicate melt infiltration into the protolith accounts for the primary variance in the Pb-Sr-Nd isotope compositions of the xenoliths and has locally generated metasomatic amphibole. Infiltration of aqueous fluids has introduced radiogenic Pb and Sr without significantly perturbing the rare earth element signature of the protolith. The Pb isotope compositions of the fluid-modified xenoliths suggest that they reacted with aqueous fluids released from a subduction zone which had equilibrated with sediment derived from an ancient basement terrain. We propose a model for mantle lithosphere evolution consistent with available textural and geochemical data for the xenolith population. The Pb-Sr-Nd isotope compositions of both alkaline mafic magmas and rare, subduction-related, calc-alkaline basaltic andesites from the region provide important constraints for the nature of the asthenospheric mantle wedge and confirm the presence of a HIMU plume component. These silicate melts contribute to the metasomatism of the mantle lithosphere rather than being derived therefrom.

Eclogitic inclusions in diamonds: Evidence of complex mantle processes over time

NASA Astrophysics Data System (ADS)

Taylor, Lawrence A.; Snyder, Gregory A.; Crozaz, Ghislaine; Sobolev, Vladimir N.; Yefimova, Emiliya S.; Sobolev, Nikolai V.

1996-08-01

The first ion-probe trace element analyses of clinopyroxene-garnet pairs both included within diamonds and from the eclogite host xenoliths are reported; these diamondiferous eclogites are from the Udachnaya and Mir kimberlite pipes, Yakutia, Russia. The major and trace element analyses of these diamond-inclusion and host-rock pairs are compared in order to determine the relative ages of the diamonds, confirm or deny genetic relationships between the diamonds and the eclogites, evaluate models of eclogite petrogenesis, and model igneous processes in the mantle before, during, and after diamond formation. The most striking aspect of the chemical compositions of the diamond inclusions is the diversity of relationships with their eclogite hosts. No single distinct pattern of variation from diamond inclusion minerals to host minerals is found for all four samples. Garnet and clinopyroxene inclusions in the diamonds from two samples (U-65/3 and U-66/3) have lower Mg#s, lower Mg, and higher Fe contents, and lower LREE than those in the host eclogite. We interpret such variations as due to metasomatism of the host eclogite after diamond formation. One sample, U-41/3 shows enrichment in diamond-inclusion MREE enrichment relative to the eclogite host and may indicate a metasomatic event prior to, or during, diamond formation. Bulanova [2] found striking differences between inclusions taken from within different portions of the very same diamond. Clinopyroxene inclusions taken from the central (early) portions of Yakutian diamonds were lower in Mg# and Mg contents (by up to 25%) than those later inclusions at the rims of diamonds. These trends are parallel to those between diamond inclusions and host eclogites determined for four of the five samples from the present study and may merely represent changing magmatic and/or P-T conditions in the mantle. Garnet trace element compositions are similar in relative proportions, but variable in abundances, between diamond inclusions and host eclogites. This is probably due to the rapid diffusion of trace elements in garnet under mantle temperatures and consequent alteration of the garnet, and not due to juvenile diamonds 'locking in' source heterogeneities (c.f., [3]). Trace element compositions of clinopyroxenes included in diamonds are generally similar to those in the host eclogite. However, one host clinopyroxene does show enrichment in the LREE compared to that in the inclusion and may be attributed to mantle metasomatism, not related to kimberlite transport. In another eclogite, M-46, the host clinopyroxene is depleted in the LREE and Fe, and enriched in the HREE and Mg, relative to the inclusion and is consistent with partial melting of the eclogite subsequent to diamond formation. Sm/Nd ratios in clinopyroxenes appear to be little affected by these processes for most samples, allowing SmNd isotopic studies to yield important information about ancient protoliths. Eclogitic mineral inclusions in Yakutian diamonds appear consanguineous with the diamonds, a contention supported by the observations of Bulanova [2]. Therefore, ReOs whole-rock and Sm/Nd clinopyroxene age determinations of the Udachnaya eclogites also yield the time of diamond formation, approximately 2.9 Ga [32,33].

Lead isotope relations in oceanic Ridge basalts from the Juan de Fuca-Gorda Ridge area N.E. Pacific Ocean

USGS Publications Warehouse

Church, S.E.; Tatsumoto, M.

1975-01-01

Lead isotopic analyses of a suite of basaltic rocks from the Juan de Fuca-Gorda Ridge and nearby seamounts confirm an isotopically heterogeneous mantle known since 1966. The process of mixing during partial melting of a heterogeneous mantle necessarily produces linear data arrays that can be interpreted as secondary isochrons. Moreover, the position of the entire lead isotope array, with respect to the geochron, requires that U/Pb and Th/Pb values are progressively increased over the age of the earth. Partial melting theory also dictates analogous behavior for the other incompatible trace elements. This process explains not only the LIL element character of MOR basalts, but also duplicates the spread of radiogenic lead data collected from alkali-rich oceanic basalts. This dynamic, open-system model of lead isotopic and chemical evolution of the mantle is believed to be the direct result of tectonic flow and convective overturn within the mantle and is compatible with geophysical models of a dynamic earth. ?? 1975 Springer-Verlag.

Geochemistry of Archean Mafic Amphibolites from the Amsaga Area, West African Craton, Mauritania: Occurrence of Archean oceanic plateau

NASA Astrophysics Data System (ADS)

El Atrassi, Fatima; Debaille, Vinciane; Mattielli, Nadine; Berger, Julien

2015-04-01

While Archean terrains are mainly composed of a TTG (Tonalite-trondhjemite-granodiorite) suite, more mafic lithologies such as amphibolites are also a typical component of those ancient terrains. Although mafic rocks represent only ~10% of the Archean cratons, they may provide key evidence of the role and nature of basaltic magmatism in the formation of the Archean crust as well as the evolution of the Archean mantle. This study focuses on the Archean crust from the West African craton in Mauritania (Amsaga area). The Amsaga Archean crust mainly consists of TTG and thrust-imbricated slices of mafic volcanic rocks, which have been affected by polymetamorphic events from the amphibolite to granulite facies. We report the results of a combined petrologic, Sm-Nd isotopic, major element and rare earth element (REE) study of the Archean amphibolites in the West African craton. This study was conducted in order to characterize these rocks, to constrain the time of their formation and to evaluate their tectonic setting and their possible mantle source. Our petrological observations show that these amphibolites have fine to medium granoblastic and nematoblastic textures. They are dominated by amphibolite-facies mineral assemblages (mainly amphibole and plagioclase), but garnet and clinopyroxene occur in a few samples. These amphibolites have tholeiitic basalt composition. On a primitive mantle-normalized diagram, they display fairly flat patterns without negative anomalies for either Eu or Nb-Ta. We have shown using Sm-Nd whole rock isotopic data that these amphibolites formed at 3.3 ±0.075 Ga. They have positive ɛNdi values (+5.2 ± 1.6). These samples show isotopically juvenile features, which rule out the possibility of significant contamination of the protolith magmas by ancient continental crust. Based on these geochemical data we propose that the tholeiitic basalts were formed in an oceanic plateau tectonic setting from a mantle plume source and that they have a depleted mantle source. It is the first time that such a signature is observed in the Archean part of the West African craton, and would suggest a widespread bimodal distribution of trace elements signature in all Archean basalts.

Heterogeneity in mantle carbon content from CO2-undersaturated basalts

PubMed Central

Le Voyer, M.; Kelley, K.A.; Cottrell, E.; Hauri, E.H.

2017-01-01

The amount of carbon present in Earth's mantle affects the dynamics of melting, volcanic eruption style and the evolution of Earth's atmosphere via planetary outgassing. Mantle carbon concentrations are difficult to quantify because most magmas are strongly degassed upon eruption. Here we report undegassed carbon concentrations from a new set of olivine-hosted melt inclusions from the Mid-Atlantic Ridge. We use the correlations of CO2 with trace elements to define an average carbon abundance for the upper mantle. Our results indicate that the upper mantle carbon content is highly heterogeneous, varying by almost two orders of magnitude globally, with the potential to produce large geographic variations in melt fraction below the volatile-free solidus. Such heterogeneity will manifest as variations in the depths at which melt becomes interconnected and detectable, the CO2 fluxes at mid-ocean ridges, the depth of the lithosphere-asthenosphere boundary, and mantle conductivity. PMID:28082738

Rare earth element selenochemistry of immiscible liquids and zircon at Apollo 14 - An ion probe study of evolved rocks on the moon

NASA Technical Reports Server (NTRS)

Snyder, Gregory A.; Taylor, Lawrence A.; Crozaz, Ghislaine

1993-01-01

Results are presented of trace-element analyses of three lunar zircons. The major-element and REE compositions were determined using electron microprobes, and a correction was made for zircon for Zr-Si-O molecular interferences in the La to Pr mass region. The three zircons were found to exhibit similar REE abundances and patterns. Results of the analyses confirm earlier studies (Hess et al., 1975; Watson, 1976; Neal and Taylor, 1989) on the partitioning behavior of trace elements in immiscible liquid-liquid pairs. The results also support the postulated importance of silicate liquid immiscibility in the differentiation of the upper mantle and crust of the moon.

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)

Major and Trace Element Analysis of Natural and Experimental Igneous Systems using LA-ICP-MS

NASA Technical Reports Server (NTRS)

Jenner, Frances E.; Arevalo, Ricardo D., Jr.

2016-01-01

Major- and trace-element compositions of minerals provide valuable information on a variety of global Earth-system processes, including melting of distinct mantle reservoirs, the growth and evolution of the Earths crust and the formation of economically viable ore deposits. In the mid-1980s and early 1990s, attempts were made to couple laser ablation (LA) systems to inductively coupled plasma mass spectrometry (ICPMS) instruments (e.g. Fryer et al. 1995; Jackson et al. 1992). The goal was to develop a rapid, highly sensitive in situ analytical technique to measure abundances and spatial distributions of trace elements in minerals and other geological samples. Elemental analysis using LAICPMS was envisaged as a quicker and less destructive means of chemical analysis (requiring only g quantities) than labour-intensive sample digestion and solution analysis (requiring mg-levels of material); and it would be a more cost-effective method than secondary ion mass spectrometry (SIMS) for the routine analysis of trace elements from solid samples. Furthermore, it would have lower limits-of-detection than electron probe microanalysis (EPMA) (e.g. Jackson et al. 1992; Eggins 2003).

Origin of cratonic lithospheric mantle roots: A geochemical study of peridotites from the North Atlantic Craton, West Greenland

NASA Astrophysics Data System (ADS)

Wittig, N.; Pearson, D. G.; Webb, M.; Ottley, C. J.; Irvine, G. J.; Kopylova, M.; Jensen, S. M.; Nowell, G. M.

2008-09-01

A critical examination of the extent to which geodynamic information on the initial mantle depletion and accretion event(s) is preserved in kimberlite-borne cratonic SCLM peridotite xenoliths is attempted by using new major and trace element data of whole-rock peridotites ( n = 55) sampled across the North Atlantic Craton (NAC; West Greenland). We also present additional whole-rock trace element data of mantle xenoliths from Somerset Island, the Slave and Kaapvaal cratons for comparison. Peridotites comprising the West Greenland SCLM are distinctly more olivine-rich and orthopyroxene-poor than most other cratonic peridotites, in particular those from the Kaapvaal craton. The West Greenland peridotites have higher Mg/Si but lower Al/Si, Al 2O 3 and CaO than cratonic mantle from the Kaapvaal Craton. We suggest that the more orthopyroxene depleted, harzburgite to dunite character of the NAC peridotites reflects more of the original melting history than peridotites from other cratons and in that sense may be more typical of cratonic lithosphere compositions prior to extensive modification. Despite this, some modal and cryptic metasomatism has clearly taken place in the West Greenland lithosphere. The insensitivity of major elements to pressure of melting at high degrees of melt extraction combined with the ease with which these elements may be changed by modal metasomatism mean that we cannot confidently constrain the depth of melting of peridotites using this approach. Mildly incompatible trace elements offer much more promise in terms of providing geodynamic information about the original Archean melting regime. The very low, systematically varying heavy REE abundances in NAC whole-rock peridotites and in peridotites from all other cratons where high-quality data are available provide ubiquitous evidence for a shallow melting regime in the absence of, or to the exhaustion of garnet. This finding explicitly excludes large extents of deep (iso- and polybaric) melting, which results in high initial garnet abundances and increasing heavy REE abundances. This evidence renders models that invoke large plume-like melting environments redundant in explaining SCLM formation and suggests broadly modern plate tectonic environments are responsible for the depletion of cratonic SCLM. A combination of the shallow melting environment and uniformly high levels of depletion indicate that melting to form the NAC lithosphere and that of other cratons probably took place in a subduction-zone environment.

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.

Origin Of Extreme 3He/4He Signatures In Icelandic Lavas: Insights From Melt Inclusion Studies

NASA Astrophysics Data System (ADS)

Harlou, R.; Kent, A. J.; Breddam, K.; Davidson, J. P.; Pearson, D. G.

2003-12-01

Helium isotopes are considered a powerful tool for tracking different mantle domains. Yet, the origin of He isotope variations in many basaltic suites remains enigmatic and often difficult to link with more lithophile chemical and isotopic tracers. One problem is that He isotope ratios are measured from crushed olivines and thus reflect prior fluid and melt fluxes trapped in inclusions within the olivine grains, whereas the lithophile elements mainly reflect the host lava. In an attempt to link He and lithophile element variations, we have characterized the major and trace element composition including volatile elements, of olivine-hosted melt inclusions from three ankaramitic lavas from Vestfirdir, NW-Iceland. Previous studies have reported extreme 3He/4He ratios from NW-Iceland and one ankaramite (SEL97) has been suggested to provide the most precise estimate of the radiogenic (Sr-Nd-Pb) isotopic composition of a relatively undegassed (high 3He/4He) mantle component (C or FOZO) common to several ocean islands (Hilton et al. 1999, EPSL 173, 53-60). The samples investigated here exhibit amongst the highest 3He/4He ratios observed in terrestrial rocks (42.9 and 34.8 R/Ra). A detailed account of the trace element signature of melt inclusions in these samples may thus help explain the origin of FOZO. One sample of similar composition to these, has a lower He content and a relatively poorly defined He isotope composition of 8.15 +/- 5.1 R/Ra (Breddam & Kurz, 2001, EOS, 82, F1315). In terms of major elements, the whole rock data reflect olivine accumulation, whereas the melt inclusion data reflect ol + cpx fractionation. The melt inclusions are generally basaltic (Mg#: 52-62), with primitive mantle normalised trace element concentrations that are broadly parallel the host lavas. There is little compositional difference between melt inclusion populations from high and low 3He/4He lavas, although inclusions of the low 3He/4He lava have lower S and moderately lower Cl. The observed range of trace element ratios: [La/Sm]N 1-4, [La/Yb]N 1-5, Sr/Nd 14-24, Ba/Rb 9-23, and Ce/Pb 5-46, covers much of the range observed in Icelandic alkali basalts. The compositional similarities between inclusions and host lavas suggests that bulk rock compositions are petrogenetically related to the melts sampled by melt inclusions. If He predominantly resides in these inclusions, it suggests that the whole rock composition is an aggregate derived from the same melts that contain the measured He.

Ca. 2.7 Ga ferropicritic magmatism: A record of Fe-rich heterogeneities during Neoarchean global mantle melting

NASA Astrophysics Data System (ADS)

Milidragovic, Dejan; Francis, Don

2016-07-01

Although terrestrial picritic magmas with FeOTOT ⩾13 wt.% are rare in the geological record, they were relatively common ca. 2.7 Ga during the Neoarchean episode of enhanced global growth of continental crust. Recent evidence that ferropicritic underplating played an important role in the ca. 2.74-2.70 Ga reworking of the Ungava craton provides the impetus for a comparison of ca. 2.7 Ga ferropicrite occurrences in the global Neoarchean magmatic record. In addition to the Fe-rich plutons of the Ungava craton, volumetrically minor ferropicritic flows, pyroclastic deposits, and intrusive rocks form parts of the Neoarchean greenstone belt stratigraphy of the Abitibi, Wawa, Wabigoon and Vermillion domains of the southern and western Superior Province. Neoarchean ferropicritic rocks also occur on five other Archean cratons: West Churchill, Slave, Yilgarn, Kaapvaal, and Karelia; suggesting that ca. 2.7 Ga Fe-rich magmatism was globally widespread. Neoarchean ferropicrites form two distinct groups in terms of their trace element geochemistry. Alkaline ferropicrites have fractionated REE profiles and show no systematic HFSE anomalies, broadly resembling the trace element character of modern-day ocean island basalt (OIB) magmas. Magmas parental to ca. 2.7 Ga alkaline ferropicrites also had high Nb/YPM (>2), low Al2O3/TiO2 (<8) and Sc/Fe (⩽3 × 10-4) ratios, and were enriched in Ni relative to primary pyrolite mantle-derived melts. The high Ni contents of the alkaline ferropicrites coupled with the low Sc/Fe ratios are consistent with derivation from olivine-free garnet-pyroxenite sources. The second ferropicrite group is characterized by decisively non-alkaline primary trace element profiles that range from flat to LREE-depleted, resembling Archean tholeiitic basalts and komatiites. In contrast to the alkaline ferropicrites, the magmas parental to the subalkaline ferropicrites had flat HREE, lower Nb/YPM (<2), higher Al2O3/TiO2 (8-25) and Sc/Fe (⩾4 × 10-4) ratios, and were depleted in Ni relative to melts of pyrolitic peridotite; suggesting they were derived from garnet-free peridotite sources. Neodymium isotopic evidence indicates that the source of alkaline ferropicrites was metasomatically enriched shortly before magma generation (⩽3.0 Ga), but the subalkaline ferropicrites do not show evidence of precursor metasomatism. The metasomatic enrichment of the alkaline ferropicrite sources may have been accompanied by conversion of Fe-rich peridotite to secondary garnet-pyroxenite. Melting experiments on ;pyrolitic; compositions and consideration of the dependence of the density of silicate liquids on pressure and temperature, suggest that ferropicrites cannot originate by melting of normal terrestrial mantle (Mg-number = 0.88-0.92) at high pressures and temperatures. The geochemical similarity between the subalkaline ferropicrites and the shergottite-nakhlite-chassigny (SNC) and howardite-eucrite-diogenite (HED) differentiated meteorites suggests, however, that the Fe-rich mantle may originate from the infall of Fe-rich chondritic meteorites. The occurrence of ca. 2.7 Ga Fe-rich rocks on at least six cratons that are commonly coeval with the more ubiquitous komatiites and Mg-tholeiites is consistent with the existence of heterogeneous Fe-rich ;plums; throughout the Neoarchean mantle. The paucity of ferropicrites in the post-2.7 Ga geological record suggests that majority of these Fe-rich plums have been melted out during the global Neoarchean melting of the mantle.

Geochemical Constraints on the Size of the Moon — Forming Giant Impact

NASA Astrophysics Data System (ADS)

Piet, H.; Badro, J.; Gillet, P.

2018-05-01

We use the partitioning of siderophile trace elements to model the geochemical influence of the Moon-forming giant impact on Earth’s mantle during core formation. We find the size of the impactor to be 15% of Earth mass or smaller.

Markov Chain Monte Carlo Inversion of Mantle Temperature and Composition, with Application to Iceland

NASA Astrophysics Data System (ADS)

Brown, Eric; Petersen, Kenni; Lesher, Charles

2017-04-01

Basalts are formed by adiabatic decompression melting of the asthenosphere, and thus provide records of the thermal, chemical and dynamical state of the upper mantle. However, uniquely constraining the importance of these factors through the lens of melting is challenging given the inevitability that primary basalts are the product of variable mixing of melts derived from distinct lithologies having different melting behaviors (e.g. peridotite vs. pyroxenite). Forward mantle melting models, such as REEBOX PRO [1], are useful tools in this regard, because they can account for differences in melting behavior and melt pooling processes, and provide estimates of bulk crust composition and volume that can be compared with geochemical and geophysical constraints, respectively. Nevertheless, these models require critical assumptions regarding mantle temperature, and lithologic abundance(s)/composition(s), all of which are poorly constrained. To provide better constraints on these parameters and their uncertainties, we have coupled a Markov Chain Monte Carlo (MCMC) sampling technique with the REEBOX PRO melting model. The MCMC method systematically samples distributions of key REEBOX PRO input parameters (mantle potential temperature, and initial abundances and compositions of the source lithologies) based on a likelihood function that describes the 'fit' of the model outputs (bulk crust composition and volume and end-member peridotite and pyroxenite melts) relative to geochemical and geophysical constraints and their associated uncertainties. As a case study, we have tested and applied the model to magmatism along Reykjanes Peninsula in Iceland, where pyroxenite has been inferred to be present in the mantle source. This locale is ideal because there exist sufficient geochemical and geophysical data to estimate bulk crust compositions and volumes, as well as the range of near-parental melts derived from the mantle. We find that for the case of passive upwelling, the models that best fit the geochemical and geophysical observables require elevated mantle potential temperatures ( 120 °C above ambient mantle), and 5% pyroxenite. The modeled peridotite source has a trace element composition similar to depleted MORB mantle, whereas the trace element composition of the pyroxenite is similar to enriched mid-ocean ridge basalt. These results highlight the promise of this method for efficiently exploring the range of mantle temperatures, lithologic abundances, and mantle source compositions that are most consistent with available observational constraints in individual volcanic systems. 1 Brown and Lesher (2016), G-cubed, 17, 3929-3968

The behaviour of tungsten during mantle melting revisited with implications for planetary differentiation time scales

NASA Astrophysics Data System (ADS)

Babechuk, Michael G.; Kamber, Balz S.; Greig, Alan; Canil, Dante; Kodolányi, János

2010-02-01

Tungsten is a moderately siderophile high-field-strength element that is hydrophile and widely regarded as highly incompatible during mantle melting. In an effort to extend empirical knowledge regarding the behaviour of W during the latter process, we report new high-precision trace element data (W, Th, U, Ba, La, Sm) that represent both terrestrial and planetary reservoirs: MORB (11), abyssal peridotites (8), eucrite basalts (3), and carbonaceous chondrites (8). A full trace element suite is also reported for Cordilleran Permian ophiolite peridotites (12) to better constrain the behaviour of W in the upper mantle. In addition, we report our long-term averages for a number of USGS (BIR-1, BHVO-1, BHVO-2, PCC-1, DTS-1) and GSJ (JA-3, JP-1) standard reference materials, some of which we conclude to be heterogeneous and contaminated with respect to W. The most significant finding of this study is that many of the highly depleted upper mantle peridotites contain far higher W concentrations than expected. In the absence of convincing indications for alteration, re-enrichment or contamination, we propose that the W excess was caused by retention in an Os-Ir alloy phase, whose stability is dependent on fO 2 of the mantle source region. This explanation could help to account for the particularly low W content of N-MORB and implies that the lithophile behaviour of W in basaltic rocks is not an accurate representation of the behaviour in the melt source. These findings then become relevant to the interpretation of W-isotopic data for achondrites, where the fractionation of Hf from W during melting is used to infer the Hf/W of the parent body mantle. This is exemplified by the differentiation chronology of the eucrite parent body (EPB), which has been modeled with a melt source with high Hf/W. By contrast, we explore the alternative scenario with a low mantle Hf/W on the EPB. Using available eucrite literature data, a maximum core segregation age of 1.2 ± 1.2 Myr after the closure of CAIs is calculated with a more prolonged time between core formation and mantle fractionation of ca. 2 Myr. This timeline is consistent with most recent published chronologies of the EPB differentiation based on the 53Mn- 53Cr and 26Al- 26Mg systems.

Linking Upper Mantle Processes and Long-wavelength Topographic Swells in Cenozoic Africa

NASA Astrophysics Data System (ADS)

Nixon, S.; Maclennan, J.; White, N.; Fishwick, S.

2008-12-01

The topography of present day Africa is influenced by two different wavelengths of dynamic support. The South African Superplume sits beneath Sub-equatorial Africa and is thought to be supported by a lower mantle thermo-chemical anomaly. On a smaller scale a series of topographic domal swells, 1000km in diameter, occur across the continent. The swells are characterised by elevated dynamic topography, a positive long-wavelength gravity anomaly and a negative velocity perturbation from a higher mode surface wave tomography model. In addition, where the lithosphere is thinner than 100km, the swells are capped with volcanic products, erupted periodically since ~30 Ma. These areas include the Cameroon Volcanic line, Hoggar, Tibesti and Darfur in North Africa, and the Ethiopian Plateau and the Kenyan dome found along the East African Rift system. The given relationships suggest the domal swells result from and are supported by upper mantle convection. In order to investigate these relationships a database of 3000 geochemical analyses has been assembled for Cenozoic African volcanism, from both literature search and by new analyses of samples collected from the Al Haruj volcanic field in Libya. Incompatible trace element ratios and REE trends from primitive basalts (>7wt% MgO) erupted less then 10Ma, representing the products of mantle melting, are compared with the upper mantle velocity structure. At depths of 75-100km the greatest velocity perturbation is associated with the Afar/Ethiopia region, where as smaller perturbations are found beneath the North African swells of Hoggar, Tibesti and Darfur. The comparison of absolute velocities, taken from the higher mode tomography model, with trace element ratios has found the low seismic velocity Afar/Ethiopia region to have shallow melting at high melt fractions (La/Yb~9) whereas North African swells with faster seismic velocities at 100 km depth, show deeper melting with smaller melt fractions (La/Yb~30). This positive correlation continues to depths of 150km and is believed to represent variations in mantle potential temperature beneath the African continent. With further modelling of major, trace and REE data we hope to provide insights into variations in mantle potential temperature, melt fraction and velocity structure beneath the topographic swells across the African continent.

Crustal Anatexis by Upwelling Mantle Melts in the N.Atlantic Igneous Province: the Isle of Rum, NW Scotland.

NASA Astrophysics Data System (ADS)

Hertogen, J.; Meyer, R.; Nicoll, G.; Troll, V. R.; Ellam, R. M.; Emeleus, C. H.

2008-12-01

Crustal anatexis is a common process in the rift-to-drift evolution during continental breakup and the formation of Volcanic Rifted Margins (VRM) systems. 'Early felsic-later mafic' volcanic rock associations on the Continent Ocean Boundary (COB) of the N.Atlantic Ocean have been sampled by ODP drilling on the SE Greenland margin and the the Vøring Plateau (Norwegian Sea). Such associations also occur further inland in the British Paleocene Igneous Province, such as on the Isle of Rum (e.g., Troll et al., Contrib. Min. Petrol., 2004, 147, p.722). Sr and Nd isotope and trace element geochemistry show that the Rum rhyodacites are the products of melting of Lewisian amphibolite gneiss. There are no indications of a melt contribution from Lewisian granulite gneiss. The amphibolite gneiss parent rock had experienced an ancient Cs and Rb loss, possibly during a Caledonian event, which caused 87Sr/86Sr heterogeneity in the crustal source of silicic melts. The dacites and early gabbros of Rum are mixtures of crustal melts and primary mantle melts. Rare Earth Element modelling shows that late stage picritic melts on Rum are close analogues for the parent melts of the Rum Layered Suite, and for the mantle melts that caused crustal anatexis of the Lewisian gneiss. These primary mantle melts have close affinities to MORB whose trace element content varies from slightly depleted to slightly enriched. The 'early felsic-later mafic' volcanic associations from Rum, and from the now drowned seaward dipping wedges on the shelf of SE Greenland and on the Vøring Plateau show geochemical differences that result from variations in the regional crustal composition and the depth at which crustal anatexis took place.

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.

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.

Magma source evolution beneath the Caribbean oceanic plateau: New insights from elemental and Sr-Nd-Pb-Hf isotopic studies of ODP Leg 165, Site 1001 basalts

NASA Astrophysics Data System (ADS)

Kerr, A. C.; Pearson, G.; Nowell, G.

2008-12-01

Ocean Drilling Project Leg 165 sampled 38m of the basaltic basement of the Caribbean plate at Site 1001 on the Hess Escarpment. The recovered section consists of 12 basaltic flow units which yield a weighted mean Ar-Ar age of 80.9±0.9 Ma (Sinton et al., 2000). The basalts (6.4-8.5 wt.% MgO) are remarkably homogeneous in composition and are more depleted in incompatible trace elements than N-MORB. Markedly, depleted initial radiogenic isotope ratios reveal a long-term history of depletion. Although the Site 1001 basalts are superficially similar to N-MORB, radiogenic isotopes in conjunction with incompatible trace element ratios show that the basalts have more similarity to the depleted basalts and komatiites of Gorgona Island. This chemical composition strongly implies that the Site 1001 basalts are derived from a depleted mantle plume component and not from depleted ambient upper mantle. Therefore the Site 1001 basalts are, both compositionally and tectonically, a constituent part of the Caribbean oceanic plateau. Mantle melt modelling suggests that the Site 1001 lavas have a composition which is consistent with second-stage melting of compositionally heterogeneous mantle plume source material which had already been melted, most likely to form the 90Ma basalts of the plateau. The prolonged residence (>10m.y.) of residual mantle plume source material below the region, confirms computational model predictions and places significant constraints on tectonic models of Caribbean evolution in the late Cretaceous, and the consequent environmental impact of oceanic plateau volcanism. Reference Sinton, C.W., et al., 2000. Geochronology and petrology of the igneous basement at the lower Nicaraguan Rise, Site 1001. Proceedings of the Ocean Drilling Program, Scientific Results. Leg 165. pp. 233-236.

Infrared trace element detection system

DOEpatents

Bien, F.; Bernstein, L.S.; Matthew, M.W.

1988-11-15

An infrared trace element detection system includes an optical cell into which the sample fluid to be examined is introduced and removed. Also introduced into the optical cell is a sample beam of infrared radiation in a first wavelength band which is significantly absorbed by the trace element and a second wavelength band which is not significantly absorbed by the trace element for passage through the optical cell through the sample fluid. The output intensities of the sample beam of radiation are selectively detected in the first and second wavelength bands. The intensities of a reference beam of the radiation are similarly detected in the first and second wavelength bands. The sensed output intensity of the sample beam in one of the first and second wavelength bands is normalized with respect to the other and similarly, the intensity of the reference beam of radiation in one of the first and second wavelength bands is normalized with respect to the other. The normalized sample beam intensity and normalized reference beam intensity are then compared to provide a signal from which the amount of trace element in the sample fluid can be determined. 11 figs.

Infrared trace element detection system

DOEpatents

Bien, Fritz; Bernstein, Lawrence S.; Matthew, Michael W.

1988-01-01

An infrared trace element detection system including an optical cell into which the sample fluid to be examined is introduced and removed. Also introduced into the optical cell is a sample beam of infrared radiation in a first wavelength band which is significantly absorbed by the trace element and a second wavelength band which is not significantly absorbed by the trace element for passage through the optical cell through the sample fluid. The output intensities of the sample beam of radiation are selectively detected in the first and second wavelength bands. The intensities of a reference beam of the radiation are similarly detected in the first and second wavelength bands. The sensed output intensity of the sample beam in one of the first and second wavelength bands is normalized with respect to the other and similarly, the intensity of the reference beam of radiation in one of the first and second wavelength bands is normalized with respect to the other. The normalized sample beam intensity and normalized reference beam intensity are then compared to provide a signal from which the amount of trace element in the sample fluid can be determined.

Tectonic Origin of Serpentinites on Syros, Greece: Geochemical Signatures of Seafloor Serpentinization Preserved in the HP/LT Subduction Complex

NASA Astrophysics Data System (ADS)

Raia, N. H.; Cooperdock, E. H. G.; Barnes, J.; Stockli, D. F.; Schwarzenbach, E. M.

2016-12-01

Serpentinized ultramafic rocks are commonly found in exhumed HP/LT subduction complexes, but their tectonic origins (i.e., setting of serpentinization) are difficult to decipher due to extensive alteration. Growing literature and geochemical datasets demonstrate that immobile elements (REE, HFSE) in serpentinites can retain magmatic signatures indicative of the tectonic setting of parent peridotite, while fluid-mobile elements and stable isotopic signatures shed light on the fluids causing serpentinization. This study combines whole-rock trace and major element geochemistry, stable isotope (δD and δO) analyses with petrographic observation to determine the tectonic origin of ultramafic rocks in the HP/LT Aegean subduction complex. The best-preserved HP rocks of the Cycladic Blueschist Unit (CBU) are found on Syros, Greece, where serpentinized ultramafic rocks within the CBU are closely associated with metamorphosed remnants of subducted oceanic crust. All samples are completely serpentinized, lacking relict pyroxene or spinel grains, with typical assemblages consisting of serpentine, talc, chlorite, magnetite, and minor carbonate. The serpentinizing fluid was characterized using stable isotopes. δD and δO values of bulk-rock serpentinite powders and chips, respectively, suggest seafloor serpentinites hydrated by seawater at low T, typical of alteration at mid-ocean ridges and hyper-extended margins (δD = -64 to -33‰ and δO = 5.2 to 9.0‰). To fingerprint a tectonic origin, whole rock serpentinite REE patterns are compared to a global database of whole rock serpentinite analyses from fore-arc mantle wedge, mid-ocean ridge, and hyper-extended margin tectonic settings. Whole rock major element, trace element, and REE analyses are consistent with limited melt extraction, flat REE patterns (LaN/SmN = 0.2-2.6, SmN/YbN = 0.3-3.5; N= C1 normalized), and do not show pronounced Eu anomalies. These data are consistent with abyssal peridotites derived from hyper-extended margin settings, although some overlap with mid-ocean ridge serpentinites makes it difficult to rule out. In any case, the geochemical signatures retained in these serpentinites indicate they are unlikely sourced from the mantle wedge, as has been historically speculated.

A Gradient in Cooling Rate Beneath the Moho at the Oman Ophiolite: Fresh Insights into Cooling Processes at Mid-Ocean Ridges from REE-Based Thermometry

NASA Astrophysics Data System (ADS)

Dygert, N. J.; Kelemen, P. B.; Liang, Y.

2015-12-01

The Wadi Tayin massif in the southern Oman ophiolite has a more than 10 km thick mantle section and is believed to have formed in a mid-ocean ridge like environment with an intermediate to fast spreading rate. Previously, [1] used major element geothermometers to investigate spatial variations in temperatures recorded in mantle peridotites and observed that samples near the paleo-Moho have higher closure temperatures than samples at the base of the mantle section. Motivated by these observations, we measured major and trace elements in orthopyroxene and clinopyroxene in peridotites from depths of ~1-8km beneath the Moho to determine closure temperatures of REE in the samples using the REE-in-two-pyroxene thermometer [2]. Clinopyroxene are depleted in LREE and have REE concentrations that vary depending on distance from the Moho. Samples nearer the Moho have lower REE concentrations than those deeper in the section (e.g., chondrite normalized Yb ranges from ~1.5 at the Moho to 4 at 8km depth), consistent with near fractional melting along a mantle adiabat. Orthopyroxene are highly depleted in LREE but measurements of middle to heavy REE have good reproducibility. We find that REE-in-two-pyroxene temperatures decrease with increasing distance from the Moho, ranging from 1325±10°C near the Moho to 1063±24°C near the base of the mantle section. Using methods from [3], we calculate cooling rates of >1000°C/Myr near the Moho, dropping to rates of <10°C/Myr at the bottom of the section. The faster cooling rate is inconsistent with conductive cooling models. Fast cooling of the mantle lithosphere could be facilitated by infiltration of seawater to or beneath the petrologic Moho. This can explain why abyssal peridotites from ultra-slow spreading centers (which lack a crustal section) have cooling rates comparable to those of Oman peridotites [3]. [1] Hanghøj et al. (2010), JPet 51(1-2), 201-227. [2] Liang et al. (2013), GCA 102, 246-260. [3] Dygert & Liang (2015), EPSL 420, 151-161.

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.

Deep solid-state equilibration and deep melting of plagioclase-free spinel peridotite from the slow-spreading Mid-Atlantic Ridge, ODP Leg 153

NASA Astrophysics Data System (ADS)

Will, Thomas M.; Schmädicke, Esther; Frimmel, Hartwig E.

2010-11-01

A petrological investigation of abyssal, plagioclase-free spinel peridotite drilled during ODP cruise 153 in the North Atlantic revealed that the peridotite represent refractory, partial residual mantle material that experienced depletion of incompatible trace elements during upper mantle melting. The degree of partial melting as estimated from spinel compositions was c. 12%. Fractionated middle and heavy rare earth elements imply polybaric melting, with c. 1-4% initial melting in the garnet peridotite stability field and subsequent partial melting of ~7-10% in the spinel peridotite stability field. Geothermobarometric investigations revealed that the solid-state equilibration of the spinel peridotite occurred at some 1,100-1,150°C and c. 20-23 kbar, corresponding to an equilibration depth of c. 70 ± 5 km and an unusually low thermal gradient of some 11-17°C/km. A thermal re-equilibration of the peridotite occurred at ~850-1,000°C at similar depths. Naturally, the initial mantle melting in the garnet-peridotite stability field must have commenced at depths greater than 70 ± 5 km. It is likely that the residual peridotite rose rapidly through the lithospheric cap towards the ridge axis. The exhumation of the abyssal peridotite occurred, at least in parts, via extensional detachment faulting. Given the shallow to moderate dip angles of the fault surfaces, the exhumation of the peridotite from its equilibration depth would imply an overall ridge-normal horizontal displacement of c. 50-160 km if tectonic stretching and detachment faulting were the sole exhumation mechanism.

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.

Interaction between Edge-Driven Convection and Mantle Plumes

NASA Astrophysics Data System (ADS)

Manjón-Cabeza Córdoba, A.; Ballmer, M.

2017-12-01

Intraplate volcanism can occur in a variety of geodynamic settings. Its characteristics can inform about the underlying mantle dynamics. A non-negligible number of intraplate oceanic volcanoes are located close to continental shelves (e.g. Bermuda, Canary Islands, Cape Verde…). In these regions, any putative plumes would interact with Edge-Driven Convection (EDC), a mode of Small-Scale Convection that is triggered along steps of lithospheric thickness. We have systematically explored 2-D geodynamic models of EDC, varying e.g. the viscosity of the mantle, geometry of the edge, potential temperature, etc. In addition, we study the influence of a mantle plume with variable excess temperature and buoyancy flux at a given distance to the edge. The mantle-convection code is coupled with a new melting parameterization that considers the depletion effect on productivity. We apply this parameterization not only to predict the extent of melting for a given lithology, but also the major-element composition of extracted melts for comparison with geochemical data. Results show that the first EDC upwellings are always localized in the oceanic domain at a distance from the continental margin that depends on mantle viscosity. The initial geometry of the edge does not have a significant influence on the "steady-state" shape of EDC. Depending on the distance of the plume from the edge and plume vigor, the plume is either deflected or enhanced by EDC. The mix of materials that melts in the mantle, as well as the amount of melting, is controlled by the interaction of the plume with EDC (e.g., with melting restricted to fertile heterogeneities in the end-member EDC case). Because several model parameters affect this interaction and related melting, a joint analysis of major-element and trace-element composition of hotspot lavas is required to constrain mantle processes.

Refertilization process in the Patagonian subcontinental lithospheric mantle of Estancia Sol de Mayo (Argentina)

NASA Astrophysics Data System (ADS)

Melchiorre, Massimiliano; Coltorti, Massimo; Gregoire, Michel; Benoit, Mathieu

2015-05-01

Anhydrous mantle xenoliths equilibrated at 1003-1040 °C from Estancia Sol de Mayo (ESM, Central Patagonia, Argentina) and entrained in post-plateau alkaline lavas belonging to Meseta Lago Buenos Aires have been investigated aiming at reconstructing the depletion and enrichment processes that affected this portion of the Patagonia lithospheric mantle. Xenoliths are characterized by a coarse-grained protogranular texture and are devoid of evident modal metasomatism. They show two texturally different clinopyroxenes: protogranular (cpx1) and texturally related to spinel (cpx2). Three different types of orthopyroxenes are also recognized: large protogranular crystals with exsolution lamellae (opx1); small clean and undeformed grains without exsolution lamellae (opx2) and small grains arranged in a vein (opx3). Major element composition of clinopyroxenes and orthopyroxenes highlights two different trends characterized by i) a high Al2O3 content at almost constant mg# and ii) a slight increase in Al2O3 content with decreasing mg#. Clinopyroxenes are enriched in LREE and are characterized by prominent to slightly negative Nb, Zr and Ti anomalies. No geochemical differences are observed between cpx1 and cpx2, while a discrimination can be observed between opx1 and opx2 (LREE-depleted; prominent to slightly negative Ti and Zr anomalies) and opx3 (prominent positive Zr anomaly). Partial melting modeling using both major and trace elements indicates a melting degree between ~ 5% and ~ 13% (up to ~ 23% according to major element modeling) for lherzolites and between ~ 20% and ~ 30% for harzburgites (down to ~ 5% according to trace element modeling). La/Yb and Al2O3, as well as Sr and Al2O3 negative correlations in clinopyroxenes point to a refertilization event affecting this lithospheric mantle. The agent was most probably a transitional alkaline/subalkaline melt, as indicated by the presence of orthopyroxene in the vein and the similar geochemical features of ESM clinopyroxenes and those from Northern Patagonia pyroxenites which are derived from transitional alkaline/subalkaline lavas.

Plume dynamics beneath the African plate inferred from the geochemistry of the Tertiary basalts of southern Ethiopia

NASA Astrophysics Data System (ADS)

George, R. M.; Rogers, N. W.

2002-09-01

Southern Ethiopian flood basalts erupted in two episodes: the pre-rift Amaro and Gamo transitional tholeiites (45-35 million years) followed by the syn-extensional Getra-Kele alkali basalts (19-11 million years). These two volcanic episodes are distinct in both trace element and isotope ratios (Zr/Nb ratios in Amaro/Gamo lavas fall between 7 and 14, and 3-4.7 in the Getra-Kele lavas whereas 206Pb/204Pb ratios fall between 18-19 and 18.9-20, respectively). The distinctive chemistries of the two eruptive phases record the tapping of two distinct source regions: a mantle plume source for the Amaro/Gamo phase and an enriched continental mantle lithosphere source for the Getra-Kele phase. Isotope and trace element variations within the Amaro/Gamo lavas reflect polybaric fractional crystallisation initiated at high pressures accompanied by limited crustal contamination. We show that clinopyroxene removal at high (0.5 GPa) crustal pressures provides an explanation for the common occurrence of transitional tholeiites in Ethiopia relative to other, typically tholeiitic flood basalt provinces. The mantle plume signature inferred from the most primitive Amaro basalts is isotopically distinct from that contributing to melt generation in central Ethiopian and Afar. This, combined with Early Tertiary plate reconstructions and similarities with Kenyan basalts farther south, lends credence to derivation of these melts from the Kenyan plume rather than the Afar mantle plume. The break in magmatism between 35 and 19 Ma is consistent with the northward movement away from the Kenya plume predicted from plate tectonic reconstructions. In this model the Getra-Kele magmatism is a response to heating of carbonatitically metasomatised lithosphere by the Afar mantle plume beneath southern Ethiopia at this time.

REE and Isotopic Compositions of Lunar Basalts Demonstrate Partial Melting of Hybridized Mantle Sources after Cumulate Overturn is Required

NASA Astrophysics Data System (ADS)

Dygert, N. J.; Liang, Y.

2017-12-01

Lunar basalts maintain an important record of the composition of the lunar interior. Much of our understanding of the Moon's early evolution comes from studying their petrogenesis. Recent experimental work has advanced our knowledge of major and trace element fractionation during lunar magma ocean (LMO) crystallization [e.g., 1-3], which produced heterogeneous basalt sources in the Moon's mantle. With the new experimental constraints, we can evaluate isotopic and trace element signatures in lunar basalts in unprecedented detail, refining inferences about the Moon's dynamic history. Two petrogenetic models are invoked to explain the compositions of the basalts. The assimilation model argues they formed as primitive melts of early LMO cumulates that assimilated late LMO cumulates as they migrated upward. The cumulate overturn model argues that dense LMO cumulates sank into the lunar interior, producing hybridized sources that melted to form the basalts. Here we compare predicted Ce/Yb and Hf and Nd isotopes of partial melts of LMO cumulates with measured compositions of lunar basalts to evaluate whether they could have formed by end-member petrogenetic models. LMO crystallization models suggest all LMO cumulates have chondrite normalized Ce/Yb <1. Residual liquid from the magma ocean has Ce/Yb 1.5. Many primitive lunar basalts have Ce/Yb>1.5; these could not have formed by assimilation of any LMO cumulate or residual liquid (or KREEP basalt, which has isotopically negative ɛNd and ɛHf). In contrast, basalt REE patterns and isotopes can easily be modeled assuming partial melting of hybridized mantle sources, indicating overturn may be required. A chemical requirement for overturn independently confirms that late LMO cumulates are sufficiently low in viscosity to sink into the lunar interior, as suggested by recent rock deformation experiments [4]. Overturned, low viscosity late LMO cumulates would be relatively stable around the core [5]. High Ce/Yb basalts require that overturned cumulates were mixed back into the overlying mantle by convection within a few hundred Myr. [1] Dygert et al. (2014), GCA 132, 170-186. [2] Sun et al. (2017), GCA 206, 273-295. [3] Lin et al. (2017), EPSL 471, 104-116. [4] Dygert et al. (2016), GRL 43, 10.1002/2015GL066546. [5] Zhang et al. (2017), GRL 44, 10.1002/2017GL073702.

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.

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.

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.

Petrogenesis of Tertiary continental intra-plate lavas between Siebengebirge and Westerwald, Germany: Constraints from trace element systematics and Nd, Sr and Pb isotopes

NASA Astrophysics Data System (ADS)

Schubert, S.; Jung, S.; Pfänder, J. A.; Hauff, F.; Garbe-Schönberg, D.

2015-10-01

New 39Ar/40Ar ages and major- and trace-element and radiogenic isotope data are presented for basanites and alkali basalts from the transition area between the Westerwald and Siebengebirge volcanic fields (Germany) that belongs to the Central European Volcanic Province (CEVP). The 39Ar/40Ar ages indicate ages of c. 24 and c. 5 Ma which are fully compatible with previous K/Ar ages indicating that the evolution of this volcanic field belongs to the Westerwald area (28-22 Ma and 5 Ma) rather than to the Siebengebirge area (26-23 Ma). Based on the occurrence of > 30 isolated volcanic plugs with a simple igneous history, this volcanic field can be viewed as a monogenetic volcanic field. Compositions of some basanites are primitive, whereas others and the alkali basalts show decreasing Cr and Ni contents and CaO/Al2O3 ratios. However, increasing TiO2, Al2O3 and incompatible elements (Sr, Zr, Y, Hf, Ta) concentrations with decreasing MgO indicating fractionation of mainly olivine with minor amounts of clinopyroxene and spinel can be noticed. Rare earth element systematics suggest that most of the alkaline rocks are generated by different degrees of melting (5%-10%) of a garnet-bearing peridotite containing some residual amphibole. Negative anomalies of Rb and K in primitive mantle-normalized diagrams and a lack of Ba/Rb fractionation suggest that amphibole was the major OH-bearing mineral phase in the mantle. The alkaline rocks have a restricted range in 87Sr/86Sr and 143Nd/144Nd ratios ranging from 0.7033 to 0.7044 and from 0.51275 to 0.51285, respectively. Lead isotope compositions (206Pb/204Pb: 19.21-19.65; 207Pb/204Pb: 15.62-15.67; 208Pb/204Pb: 39.10-39.46) of the alkaline rocks are within the range of most OIB in which the higher values approach the composition of the European Asthenospheric Reservoir (EAR). The correlation between Sr and Nd isotopes and trace element constraints (Ce/Pb; Nb/U) indicates that for some samples interaction with crustal rocks during fractionation has occurred. Miocene intraplate basaltic volcanism in the area probably occurred as a result of minor "baby plume" activity. Each volcanic plug records evidence of a specific stage of fractionation with or without assimilation; however, in summary the lavas plot on a single fractionation path. This implies that during evolution of the volcanic field initial melting took place in the asthenosphere or at the lithosphere-asthenosphere interface. The melts moved through the lithospheric mantle and stagnated at crustal levels, however the observed fractionation paths suggest that they were fed from a single reservoir. This model, which involves small-scale plume impact followed by asthenosphere-lithosphere interaction together with minor crustal contamination, should also be applicable to other intra-continental rift-related areas.

Multiple episodes of partial melting, depletion, metasomatism and enrichment processes recorded in the heterogeneous upper mantle sequence of the Neotethyan Eldivan ophiolite, Turkey

NASA Astrophysics Data System (ADS)

Uysal, Ibrahim; Ersoy, E. Yalçın; Dilek, Yildirim; Kapsiotis, Argyrios; Sarıfakıoğlu, Ender

2016-03-01

The Eldivan ophiolite along the Izmir-Ankara-Erzincan suture zone in north-central Anatolia represents a remnant of the Neotethyan oceanic lithosphere. Its upper mantle peridotites include three lithologically and compositionally distinct units: clinopyroxene (cpx)-harzburgite and lherzolite (Group-1), depleted harzburgite (Group-2), and dunite (Group-3). Relics of primary olivine and pyroxene occur in the less refractory harzburgites, and fresh chromian spinel (Cr-spinel) is ubiquitous in all peridotites. The Eldivan peridotites reflect a petrogenetic history evolving from relatively fertile (lherzolite and cpx-harzburgite) toward more depleted (dunite) compositions through time, as indicated by (i) a progressive decrease in the modal cpx distribution, (ii) a progressive increase in the Cr#s [Cr / (Cr + Al)] of Cr-spinel (0.15-0.78), and (iii) an increased depletion in the whole-rock abundances of some magmaphile major oxides (Al2O3, CaO, SiO2 and TiO2) and incompatible trace elements (Zn, Sc, V and Y). The primitive mantle-normalized REE patterns of the Group-1 and some of the Group-2 peridotites display LREE depletions. Higher YbN and lower SmN/YbN ratios of these rocks are compatible with their formation after relatively low degrees (9-25%) of open-system dynamic melting (OSDM) of a Depleted Mid-ocean ridge Mantle (DMM) source, which was then fluxed with small volumes of oceanic mantle-derived melt [fluxing ratio (β): 0.7-1.2%]. Accessory Cr-spinel compositions (Cr# = 015-0.53) of these rocks are consistent with their origin as residual peridotites beneath a mid-ocean ridge axis. Part of the Group-2 harzburgites exhibit lower YbN and higher SmN/YbN ratios, LREE-enriched REE patterns, and higher Cr-spinel Cr#s ranging between 0.54 and 0.61. Trace element compositions of these peridotites can be modeled by approximately 15% OSDM of a previously 17% depleted DMM, which was then fluxed (β: 0.4%) with subduction-influenced melt. The Group-3 dunite samples contain Cr-spinel with elevated Cr#s (0.73-0.78) and low-TiO2 contents (< 0.13 wt.%), implying higher degrees of melting (21-24%) of an already depleted DMM that was triggered by infiltration of low-Ti boninite melt with fluxing rates of 0.4-4.0%. The existence of interstitial, idiomorphic Cr-spinel (high Cr# and low Ti) in the Group-3 dunites is consistent with this interpretation. The occurrence of both MOR- and SSZ-type peridotites in the Eldivan ophiolite suggests that its heterogeneous upper mantle was produced as a result of different partial melting and melt-rock reaction processes in different tectonic settings within the Neotethyan realm.

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.

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.

Melt inclusion study of the most recent basanites from El Hierro and Lanzarote, Canary Islands

NASA Astrophysics Data System (ADS)

Gomez-Ulla, Alejandra; Sigmarsson, Olgeir; Huertas, Maria Jose; Ancochea, Eumenio

2015-04-01

The latest eruptions of both Lanzarote (one of the oldest and easternmost of the Canary Island archipelago) and El Hierro (the youngest and westernmost) produced basanite lavas. Major, volatile and trace element concentrations of melt inclusion (MI) hosted in olivine for both eruptions have been analysed. The basanites display primitive mantle normalized trace element spectra suggesting a magma source largely composed of recycled oceanic crust. In addition, beneath Lanzarote an interaction with a carbonatitic fluid phase or metasome would explain eccentric Ba/U and other trace element ratios. Contribution of carbonatitic component would readily account for extremely volatile-rich (Cl, F, S) MI from Lanzarote (Cl=1577-2500 ppm) whereas the maximum for El Hierro is 1080 ppm. The submarine character of the 2011-12 eruption off El Hierro appears to have affected the degassing behavior, whereas estimated sulfur emission to the atmosphere during the historical Lanzarote eruptions are amongst the highest observed so far. An estimated magma volume (VDRE) of 0.02 km3 yields atmospheric mass loading of 0.2 Mt SO2 from the 1824 Lanzarote eruption. Scaling the volume of the 1824 Lanzarote eruption to that of the previous Timanfaya eruption (1730-6; 5 km3) results in estimated 12 Mt SO2, an atmospheric mass loading only outnumbered by the historical Laki and Eldgjá eruptions in Iceland. The significantly greater volatile budget of basanites from Lanzarote compared to El Hierro is thus controlled by more fertile source composition closer to the African continent.

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.

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.

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.

Mantle End-Members: The Trace Element Perspective

NASA Astrophysics Data System (ADS)

Willbold, M.; Stracke, A.; Hofmann, A. W.

2004-12-01

On the basis of their isotopic composition, ocean island basalts (OIB) have been classified into three to four end-members; HIMU with the most radiogenic Pb isotope ratios of OIB and Enriched Mantle 1 and 2 (EM1, EM2) with less radiogenic but variable Pb isotope and highly radiogenic Sr isotope signatures. It has also been argued that each of these isotopic families has common trace element characteristics that distinguish them from one another and so substantiated this classification. Here, we present new high-precision trace element data for samples from St. Helena, Tristan da Cunha and Gough in the Atlantic Ocean. The overall data-set is augmented by OIB data from the GEOROC database and includes data from all major isotopic families (HIMU: St. Helena, Mangaia, Tubuai, and Rururtu; EM1: Tristan da Cunha, Gough, Pitcairn; and EM2: Samoa, Marquesas, and Society). For each locality we use only islands defining the most extreme isotopic compositions. The entire data-set has been screened to exclude altered and highly differentiated samples. HIMU basalts have a very uniform trace element composition. Compared to HIMU-type basalts, EM-type basalts are enriched in Rb, Ba, and K, and depleted in U, Nb, and Ta, relative to La. Different EM-type OIBs from the same isotopic family (EM1 or EM2), have distinct trace element characteristics that can ultimately only be caused by different source compositions. For example, Ba/Th ratios in samples from both Tristan da Cunha (EM1) and Samoa (EM2) are similarly high (ca. 110) whereas Ba/Th ratios in samples from Pitcairn (EM1) and Society (EM2) samples are consistently lower (ca. 70). Thus on the basis of their trace element composition, EM-type OIB cannot be classified into EM1 and EM2 type basalts, nor can any other grouping be identified. The remarkably uniform isotopic and trace element composition of HIMU-type basalts suggests derivation from a single common source reservoir, most likely subduction-modified oceanic crust. Although there are some trace element characteristics common to all EM-type basalts, which distinguish them from HIMU-type basalts (e.g. uniformly high Th/U ratios of 4.7 ± 0.3, and enrichment in Cs-U), each suite of EM-type basalts has unique trace element signatures that distinguish them from any other suite of EM-type basalts. This is especially obvious when comparing the trace element composition of EM basalts from one isotopic family, for example EM1-type basalts from Tristan, Gough and Pitcairn. Consequently, the trace element systematics of EM-type basalts suggest that there are many different EM-type sources, whereas the isotopic composition of EM-type basalts suggest derivation from two broadly similar sources, i.e. EM1 and EM2. The large variability in subducting sediments with respect to both parent-daughter (e.g. Rb/Sr, Sm/Nd, U/Pb, Th/Pb,...) and other trace element ratios makes it unlikely that there are reproducible mixtures of sediments leading to two different isotopic evolution paths (EM1 and EM2) while preserving a range of incompatible element contents for each isotopic family, as would be required to reconcile the isotopic and trace element characteristics of EM-type basalts. Although this does not a priori argue against sediments as possible source components for OIB, it does argue against two distinct groups of sediments as EM1 and EM2 sources. Further characterization of sources with the same general origin (e.g. a certain type of crust or lithosphere) or identification of processes leading to reservoirs with similar parent-daughter ratio characteristics but different incompatible trace element contents could resolve the apparent conundrum.

Veined pyroxenite xenoliths in Ugandan kamafugites: mantle or magma? Using in situ techniques for 87Sr/86Sr-isotopes and trace elements as tools

NASA Astrophysics Data System (ADS)

Link, Klemens; Tommasini, Simone; Braschi, Eleonora; Conticelli, Sandro; Barifaijo, Erasmus; Tiberindwa, John V.; Foley, Stephen F.

2010-05-01

The genesis of pyroxenite nodules in Ugandan kamafugites and their possible genetic relationships is a matter of debate. In earlier studies the pyroxenites were considered either as xenoliths from pervasively metasomatized peridotite mantle (Lloyd, 1981) or as distinct paragenesises occurring as veins within the peridotitic mantle (Harte et al., 1993). In both cases the xenoliths would represent mantle material that was at least partly involved as source material for the kamafugite melts. A third alternative could be that they represent cumulates of the lavas. In any case, the nodules provide important information for understanding the generation of ultrapotassic lavas and for characterizing the rift-related lithosphere mantle as part of the initial continental rift process. Originally the ultrapotassic kamafugites were considered to be single stage partial melts of pervasively metasomatized mantle but new geochemical studies indicate a multistage development (Rosenthal et al., 2009). Nd, Hf and Os isotopes point to mixing between components derived from metasomatically influenced peridotite and mica-pyroxenite. In-situ investigation of the Sr-isotope and trace element compositions of individual minerals in a number of xenoliths allows us to constrain their genesis and relation to the host lavas. The nodules appear to originate by near-liquidus crystallization of melts derived from enriched peridotite within the cratonic lithosphere mantle. They later partially remelted to form one source of the potassium-rich kamafugites. Sr-isotopes from different domains within single mineral grains in the nodules and host lavas are used to trace the nodules' role as a potential source to lavas, and trace element measurements are used to support the conclusions. Rb/Sr- measurements from the biotites to constrain the time between nodule crystallization and eruption of the Quaternary lavas to about 3.3 Ma. This also suggests a significant increase of the geothermal gradient beneath the preceding rift within that time. Structures on microscopic scale indicate at least two different generations of mineral growth clearly related to multiphase magmatic events forming the nodules. Rare composite samples allow a correlation between the older and younger parageneses, demonstrating reaction between the older matrix pyroxenite and the younger, high-Ti melt. The relatively low (~0,13wt%) Cr2O3-contents together with the high LREE concentrations measured in the oldest observed clinopyroxenes (La~12,4 x PRIMA with La/Lu~21) as well as the lack of any other characteristic mineral relicts argue against a pervasively overprinted peridotite mantle. Comparable 87Sr/86Sr- values close to bulk earth values as well as similar 143Nd/144Nd- ratios in the nodules (0,512480-0,5122573) and the lavas (average: 0,512551) support a genetic link between the kamafugites and the nodules as suggested by experiments (Lloyd et al. 1985). Low radiogenic 87Sr/86Sr ratios in Rb-free clinopyroxene and perovskite (0,704459-0,704487) constrain initial values for the source whereas slightly more radiogenic values from cogenetic Rb-bearing biotites (0,704754- 0,704762) are the result of radioactive decay after mineral growth. The majority of the kamafugite 87Sr/86Sr values lie between the two end-members (0,704624- 0,704717). Additionally considering microscale structures showing melting processes we conclude that the nodules represent one source and that the intermediate 87Sr/86Sr values of the lavas reflect the melting of differing proportions of biotite and clinopyroxene in the source region.

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.

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).

Petrogenesis of nephelinites from the Tarim Large Igneous Province, NW China: Implications for mantle source characteristics and plume-lithosphere interaction

NASA Astrophysics Data System (ADS)

Cheng, Zhiguo; Zhang, Zhaochong; Hou, Tong; Santosh, M.; Zhang, Dongyang; Ke, Shan

2015-04-01

The nephelinite exposed in the Wajilitage area in the northwestern margin of the Tarim large igneous province (TLIP), Xinjiang, NW China display porphyritic textures with clinopyroxene, nepheline and olivine as the major phenocryst phases, together with minor apatite, sodalite and alkali feldspar. The groundmass typically has cryptocrystalline texture and is composed of crystallites of clinopyroxene, nepheline, Fe-Ti oxides, sodalite, apatite, rutile, biotite, amphibole and alkali feldspar. We report rutile SIMS U-Pb age of 268 ± 30 Ma suggesting that the nephelinite may represent the last phase of the TLIP magmatism, which is also confirmed by the field relation. The nephelinite shows depleted Sr-Nd isotopic compositions with age-corrected 87Sr/86Sr and εNd(t) values of 0.70348-0.70371 and + 3.28 to + 3.88 respectively indicating asthenospheric mantle source. Based on the reconstructed primary melt composition, the depth of magma generation is estimated as 115-140 km and the temperatures of mantle melting as 1540-1575 °C. The hotter than normal asthenospheric mantle temperature suggests the involvement of mantle thermal plume. The Mg isotope values display a limited range of δ26Mg from - 0.35 to - 0.55‰, which are lower than the mantle values (- 0.25‰). The Mg isotopic compositions, combined with the Sr-Nd isotopes and major and trace element data suggest that the Wajilitage nephelinite was most likely generated by low-degree partial melting of the hybridized carbonated peridotite/eclogite source, which we correlate with metasomatism by subducted carbonates within the early-middle Paleozoic convergent regime. A plume-lithosphere model is proposed with slight thinning of the lithosphere and variable depth and degree of melting of the carbonated mantle during the plume-lithosphere interaction. This model also accounts for the variation in lithology of the TLIP.

Thermal-chemical Mantle Convection Models With Adaptive Mesh Refinement

NASA Astrophysics Data System (ADS)

Leng, W.; Zhong, S.

2008-12-01

In numerical modeling of mantle convection, resolution is often crucial for resolving small-scale features. New techniques, adaptive mesh refinement (AMR), allow local mesh refinement wherever high resolution is needed, while leaving other regions with relatively low resolution. Both computational efficiency for large- scale simulation and accuracy for small-scale features can thus be achieved with AMR. Based on the octree data structure [Tu et al. 2005], we implement the AMR techniques into the 2-D mantle convection models. For pure thermal convection models, benchmark tests show that our code can achieve high accuracy with relatively small number of elements both for isoviscous cases (i.e. 7492 AMR elements v.s. 65536 uniform elements) and for temperature-dependent viscosity cases (i.e. 14620 AMR elements v.s. 65536 uniform elements). We further implement tracer-method into the models for simulating thermal-chemical convection. By appropriately adding and removing tracers according to the refinement of the meshes, our code successfully reproduces the benchmark results in van Keken et al. [1997] with much fewer elements and tracers compared with uniform-mesh models (i.e. 7552 AMR elements v.s. 16384 uniform elements, and ~83000 tracers v.s. ~410000 tracers). The boundaries of the chemical piles in our AMR code can be easily refined to the scales of a few kilometers for the Earth's mantle and the tracers are concentrated near the chemical boundaries to precisely trace the evolvement of the boundaries. It is thus very suitable for our AMR code to study the thermal-chemical convection problems which need high resolution to resolve the evolvement of chemical boundaries, such as the entrainment problems [Sleep, 1988].

A SIMS study of lunar 'komatiitic glasses' - Trace element characteristics and possible origin

NASA Technical Reports Server (NTRS)

Shearer, C. K.; Papike, J. J.; Galbreath, K. C.; Wentworth, S. J.; Shimizu, N.

1990-01-01

In Apollo 16 regolith breccias, Wentworth and McKay (1988) identified a suite of minute (less than 120 microns) 'komatiitic glass beads'. The wide major element compositional range, and ultra-Mg-prime character of the glasses suggest a variety of possible origins from complex impact processes to complex volcanic processes involving rather unusual and primitive magmatism. The extent of trace element depletion or enrichment in these glasses appears to be correlated to the siderophile character of the element (ionization potential or experimentally determined silicate melt/Fe metal partition coefficients. The ultra-Mg-prime glasses are depleted in Co relative to a bulk Moon Mg/Co exhibited by many lunar samples (volcanic glasses, basalts, regolith breccia, estimated upper mantle). The low Co and high incompatible element concentrations diminish the possibility that these glasses are a product of lunar komatiitic volcanism or impact, excavation, and melting of a very high Mg-prime plutonic unit.

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.

Inferring the Behavior, Concentration and Flux of CO2 from the Suboceanic Mantle from Undegassed Ocean Ridge and Ocean Island Basalts

NASA Astrophysics Data System (ADS)

Michael, P. J.; Graham, D. W.

2015-12-01

We determined glass and vesicle CO2 contents, plus trace element contents for fifty-one ultradepleted mid-ocean ridge basalt (MORB) glasses distributed globally. Sixteen had no vesicles and were volatile undersaturated. Thirty-five had vesicles and were slightly oversaturated. If this latter group lost 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 they did not lose bubbles, then CO2/Nb is the most uniform ratio for the entire suite of ultradepleted MORBs at 291±132, while CO2/Ba decreases with incompatible element enrichment. For a wider range of compositions, we used published estimates of CO2 in enriched basalts that retained vesicles e.g., "popping rocks", and from melt inclusions in normal MORBs. As incompatible element enrichment increases, CO2/Nb increases from 283±32 in ultradepleted MORBs to 603±69 in depleted melt inclusions to 936±132 in enriched basalts. In contrast, CO2/Ba is nearly constant 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 anomalously high Ba and low CO2/Ba. Using the CO2/Ba ratio and an average MORB composition, the CO2 concentration of a primary, average MORB is 2085+473/-427 ppm while primary NMORB has 1840ppm CO2. The annual flux of CO2 from mid-ocean ridges is 1.25±0.16 x 1014 g/yr (0.93 - 1.61 x 1014 g/yr is possible): higher than published estimates that use CO2/3He in MORB and the abyssal ocean 3He flux. This may be accounted for by a CO2/3He ratio that is higher than the commonly accepted MORB ratio of 2x109 due to leverage by more enriched basalts. NMORB mantle has 183 ppm CO2 based on simple melting models. More realistic estimates of depleted mantle composition yield lower estimates of ~60-130ppm, with large uncertainties that depend more on melting models than on CO2/Ba. CO2/Ba is not correlated with isotopic or trace element ratios.

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.

Oxygen Isotopes in Intra-Back Arc Basalts from the Andean Southern Volcanic Zone

NASA Astrophysics Data System (ADS)

Parks, B. H.; Wang, Z.; Saal, A. E.; Frey, F. A.; Blusztajn, J.

2013-12-01

The chemical compositions of volcanic rocks from the Andean Southern Volcanic Zone (SVZ) reflect complex and dynamic interactions among the subducting oceanic lithosphere, the mantle wedge, and the overlying continental crust. Oxygen isotope ratios of olivine phenocrysts can be a useful means to identifying their relative contributions to the arc magmatism. In this study, we report high-precision oxygen-isotope ratios of olivine phenocrysts in a set of intra-back arc basalts from the SVZ. The samples were collected from monogenetic cinder cones east of the volcanic front (35-39 degrees S), and have been geochemically well-characterized with major and trace element contents, and Sr-Nd-Pb isotope compositions. Compared to lavas from the volcanic front, these intra-back arc lavas have similar radiogenic isotope, and a more alkalic and primitive (higher MgO content) chemical composition. We determined the oxygen-isotope ratios using the CO2-laser-fluorination method set up at the Department of Geology and Geophysics, Yale University following the techniques reported in Wang et al (2011). The samples were analyzed with standards of Gore Mountain Garnet (5.77×0.12‰ 1σ; Valley et al., 1995) and Kilbourne Hole Olivine (5.23×0.07‰ 1σ; Sharp, 1990) in order to account for minor changes in the vacuum line during analyses. The obtained δ18OSMOW values of olivine phenocrysts from the intra-back arc basalts vary from 4.98×0.01 to 5.34×0.01‰. This range, surprisingly, is similar to the δ18O values of olivines from mantle peridotites (5.2×0.2‰). Preliminary results indicate significant correlations of 87Sr/86Sr, 143Nd/144Nd and trace element ratios of the basaltic matrix with the δ18O values of olivine phenocrysts, indicating at least three components involved in the formation of the arc volcanism. By comparing the δ18O with the variations of major and trace element contents (e.g., MgO, TiO2 and Ni), and trace element ratios (e.g. Ba/Nb), we evaluate the effects of fractionation crystallization, crustal contamination, the extent of slab flux, metasomatism, and melting of the mantle wedge on the intra-back arc lavas from the SVZ.

Genesis of Ultra-High Pressure Garnet Pyroxenite in Orogenic Peridotites and its bearing on the Isotopic Chemical Heterogeneity in the Mantle Source of Oceanic Basalts

NASA Astrophysics Data System (ADS)

Varas Reus, María Isabel; Garrido, Carlos J.; Marchesi, Claudio; Bosch, Delphine; Hidas, Károly

2017-04-01

The genesis of ultra-high pressure (UHP) garnet pyroxenites in orogenic peridotite massifs and its implications on the formation of chemical heterogeneities in the mantle and on basalt petrogenesis are still not fully understood. Some UHP (diamond-bearing) garnet pyroxenites have isotopic, and major and trace element compositions similar to the recycled oceanic crustal component observed in oceanic basalts [1-6]. These pyroxenites hence provide an exceptional opportunity to investigate in situ the nature and scale of the Earth's mantle chemical heterogeneities. Here, we present an integrated geochemical study of UHP garnet pyroxenites from the Ronda (Betic Belt, S. Spain) and Beni Bousera (Rif Belt, N. Morocco) peridotite massifs. This investigation encompasses, in the same sample, bulk rock major and trace elements, as well as Sr-Nd-Pb-Hf isotopic analyses. According to their Al2O3 content, we classify UHP garnet pyroxenites into three groups that have distinct trace elements and Sr-Nd-Pb-Hf isotopic signatures. Group A pyroxenites (Al2O3: 15 - 17.5 wt. %) are characterized by low initial 87Sr/86Sr, relatively high 143Nd/144Nd, 206Pb/204Pb and 176Hf/177Hf ratios, and highly variable 207Pb/204Pb and 208Pb/204Pb ratios. Group B pyroxenites (Al2O3 < 14 wt. %) have isotopic signatures characterized by relatively high initial 87Sr/86Sr and low 143Nd/144Nd, 206Pb/204Pb and 176Hf/177Hf ratios. Group C pyroxenites (Al2O3 ˜ 15 wt. %) display relatively low initial 87Sr/86Sr and 206Pb/204Pb ratios, high 143Nd/144Nd and 176Hf/177Hf ratios, and 207Pb/204Pb and 208Pb/204Pb ratios similar to Group B pyroxenites. The major and trace element, and isotopic compositions of the studied Ronda and Beni Bousera UHP garnet pyroxenites lend support to the "Marble Cake Mantle" model [7] for the genesis of these pyroxenites. This model envisions the mantle source of oceanic basalts as a mélange of subducted, ancient oceanic crust —-represented by garnet pyroxenites in orogenic peridotites—- intimately mixed with peridotites by mantle convection. The present study reveals, however, that besides this exotic component of ancient recycled oceanic crust, the genesis of these pyroxenites requires a previously unnoticed component of recycled lower continental crust akin to the lower crustal section of the lithosphere where these UHP garnet pyroxenites now reside in. The results of this study provide a new recipe for the marble cake hypothesis for the genesis of UHP garnet pyroxenites in orogenic peridotites. Furthermore, it establishes a connection between the genesis of UHP pyroxenites, the composition of the continental crust and the generation of Earth's mantle heterogeneities. References: [1] Pearson, D. G., Davies, G. R. & Nixon, P. H. (1993). Geochemical constraints on the petrogenesis of diamond facies pyroxenites from the Beni Bousera peridotite massif, North Morocco. Journal of Petrology 34, 125-172. [2] Blichert-Toft, J., Albarède, F. & Kornprobst, J. (1999). Lu-Hf Isotope systematics of garnet pyroxenites from Beni Bousera, Morocco: implications for basalt origin. Science 283, 1303-1306. [3] Garrido, C. J. & Bodinier, J. L. (1999). Diversity of mafic rocks in the Ronda peridotite: Evidence for pervasive melt-rock reaction during heating of subcontinental lithosphere by upwelling asthenosphere. Journal of Petrology 40, 729-754. [4] Marchesi, C., Garrido, C.J., Bosch, D., Bodinier, J.-L., Gervilla, F., Hidas, K., 2013. Mantle refertilization by melts of crustal-derived garnet pyroxenite: Evidence from the Ronda peridotite massif, southern Spain. Earth and Planetary Science Letters 362, 66-75. doi: 10.1016/j.epsl.2012.11.047. [5] Marchesi, C., Dale, C.W., Garrido, C.J., Pearson, D.G., Bosch, D., Bodinier, J.-L., Gervilla, F., Hidas, K., 2014. Fractionation of highly siderophile elements in refertilized mantle: Implications for the Os isotope composition of basalts. Earth and Planetary Science Letters 400, 33-44. doi: 10.1016/j.epsl.2014.05.025 [6] Montanini, A. & Tribuzio, R. (2015). Evolution of recycled crust within the mantle: Constraints from the garnet pyroxenites of the External Ligurian ophiolites (northern Apennines, Italy). Geology 43, 911-914. [7] Allègre, C. J. & Turcotte, D. L. (1986). Implications of a two-component marble-cake mantle. Nature 323, 123-127.

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.

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.

Sr, Nd, Pb and Hf Isotopic Compositions of Late Cenozoic Alkali Basalts in South Korea: Evidence for Mixing Between the Two Dominant Asthenospheric Mantle Domains beneath East Asia

NASA Astrophysics Data System (ADS)

Choi, S.; Mukasa, S. B.; Kwon, S.; Andronikov, A. V.

2004-12-01

We determined the Sr, Nd, Pb and Hf isotopic compositions of late Cenozoic basaltic rocks from six lava-field provinces in South Korea, including Baengnyeong Island, Jogokni, Ganseong area, Jeju Island, Ulleung Island and Dog Island, in order to understand the nature of the mantle source. The basalts have OIB-like trace element abundance patterns, and also contain mantle-derived xenoliths. Available isotope data of late Cenozoic basalts from East Asia, along with ours, show that the mantle source has a DMM-EM1 array for northeast China and a DMM-EM2 array for Southeast Asia. We note that the basalts falling on an array between DMM and an intermediate end member between EM1 and EM2, are located between the two large-scale isotopic provinces, i.e., around the eastern part of South Korea. The most intriguing observation on the isotopic correlation diagrams is spatial variation from predominantly EM2 signatures in the basaltic lavas toward increasingly important addition of EM1, starting from Jeju Island to Ulleung and Dog Islands to Ganseong area, and to Baengnyeong Island. This is without any corresponding changes in the basement and the lithospheric mantle beneath the region. These observations suggest that the asthenospheric mantle source is dominant for the Cenozoic intraplate volcanism in East Asia, which is characterized by two distinct, large-scale domains. Previous studies on East Asian Cenozoic volcanic rocks have invoked origins by either plume activity or decompressional melting in a rift environment. On the basis of our new trace element and isotopic compositions which have OIB-like characteristics, we prefer a plume origin for these lavas. However, because tomographic images do not show distinct thermal anomaly that would be interpreted as a plume, we suggest that the magmatism might be the product of small, difficult to image multiple plumes that tapped the shallow part of the asthenosphere (probably the transition zone in the upper mantle).

Petrogenesis of the Dalongkai ultramafic-mafic intrusion and its tectonic implication for the Paleotethyan evolution along the Ailaoshan tectonic zone (SW China)

NASA Astrophysics Data System (ADS)

Liu, Huichuan; Wang, Yuejun; Zi, Jian-Wei

2017-06-01

Layered ultramafic-mafic intrusions are usually formed in an arc/back-arc or intra-plate tectonic environment, or genetically related to a mantle plume. In this paper, we report on an ultramafic-mafic intrusion, the Dalongkai intrusion in the Ailaoshan tectonic zone (SW China), whose occurrence is closely associated with arc/back-arc magmatic rocks. The Dalongkai intrusion is composed of plagioclase-lherzolite, hornblende-peridotite, lherzolite and wehrlite at the bottom, cumulate plagioclase-pyroxenite at the middle part, changing to fine-grained gabbro towards the upper part of the intrusion, forming layering structure. Zircons from the plagioclase-pyroxenites and gabbros yielded U-Pb ages of 272.1 ± 1.7 Ma and 266.4 ± 5.8 Ma, respectively. The plagioclase-pyroxenites show cumulate textures, and are characterized by high MgO (25.0-28.0 wt.%; mg# = 80.6-82.3), Cr (1606-2089 ppm) and Ni (893-1203 ppm) contents, interpreted as early cumulate phases. By contrast, the gabbros have relatively lower mg# values (56.3-62.7), and Cr (157-218 ppm) and Ni (73-114 ppm) concentrations, and may represent frozen liquids. The plagioclase-pyroxenites and gabbros share similar chondrite-normalized REE patterns and primitive mantle-normalized trace element profiles which are analogous to those of typical back-arc basin basalts. The εNd(t) values for both rock types range from +2.20 to +4.22. These geochemical and isotopic signatures suggest that the Dalongkai ultramafic-mafic rocks originated from a MORB-like mantle source metasomatized by subduction-related, sediment-derived fluids. Our data, together with other geological evidence, indicate that the emplacement of the Dalongkai ultramafic-mafic intrusion most likely occurred in a back-arc extensional setting associated with subduction of the Ailaoshan Paleotethyan branch ocean during the Middle Permian, thus ruling out the previously speculated linkage to the Emeishan mantle plume, or to an intra-continental rift.

Geochemical constraints on possible subduction components in lavas of Mayon and Taal Volcanoes, Southern Luzon, Philippines

USGS Publications Warehouse

Castillo, P.R.; Newhall, C.G.

2004-01-01

Mayon is the most active volcano along the east margin of southern Luzon, Philippines. Petrographic and major element data indicate that Mayon has produced a basaltic to andesitic lava series by fractional crystallization and magma mixing. Trace element data indicate that the parental basalts came from a heterogeneous mantle source. The unmodified composition of the mantle wedge is similar to that beneath the Indian Ocean. To this mantle was added a subduction component consisting of melt from subducted pelagic sediment and aqueous fluid dehydrated from the subducted basaltic crust. Lavas from the highly active Taal Volcano on the west margin of southern Luzon are compositionally more variable than Mayon lavas. Taal lavas also originated from a mantle wedge metasomatized by aqueous fluid dehydrated from the subducted basaltic crust and melt plus fluid derived from the subducted terrigenous sediment. More sediment is involved in the generation of Taal lavas. Lead isotopes argue against crustal contamination. Some heterogeneity of the unmodified mantle wedge and differences in whether the sediment signature is transferred into the lava source through an aqueous fluid or melt phase are needed to explain the regional compositional variation of Philippine arc lavas. ?? Oxford University Press 2004; all rights reserved.

Sr-Nd isotope geology and tectonomagmatic setting of the Dehsalm intrusives (Lut Block, Eastern Iran)

NASA Astrophysics Data System (ADS)

Arjmandzadeh, Reza; Francisco Santos, Jose; Ribeiro, Sara

2013-04-01

The Dehsalm porphyritic shallow intrusives belong to the Lut Block volcanic-plutonic belt (central eastern Iran). Previous research on alteration, mineralization and hydrothermal fluids indicates that a Cu-Mo porphyry type mineralization system is related with these intrusives (Arjmandzadeh et al., 2012). The rocks studied in this work range in composition from gabbro-diorite to granite, with dominance of monzonites and quartz monzonites, and have geochemical features of high-K calc alkaline to shoshonitic volcanic arc suites. The trends of major element oxides on Harker diagrams, together with textural evidence, point to the crystal fractionation of clinopyroxene, Ca - plagioclase, hornblende, apatite and oxide minerals. Primitive mantle - normalized trace element spider diagrams display strong enrichment in LILE, such as Rb, Ba and Cs, and depletions in some high field strength elements (HFSE), such as Nb, Ti, Y and HREE. Chondrite-normalized plots show significant LREE enrichments, high LaN/YbN (21.5 to 31.0) and the lack of Eu anomaly. Sr/Y and La/Yb ratios of Dehsalm intrusives are respectively 31.6-72.2 and 21.5-33.5, which reveals that, despite their K-rich composition, these rocks also have some adakitic affinity. A Rb-Sr whole rock-feldspar-biotite age of 33.4±1 Ma was obtained in a quartz monzonite sample; this date may be interpreted as close to the intrusion age, considering that the chosen sample is almost unaltered and should have suffered fast cooling. The obtained age coincides, within error, with a previous geochronological result in a similar rock from the Chah-Shaljami area (Arjmandzadeh et al., 2011), further northwest along the eastern border of the Lut Block. 87Sr/86Sr(33Ma) and ɛNd(33Ma) values range from 0.70481 to 0.70508 and from +1.5 to +2.5, respectively, which fits into a supra-subduction mantle wedge source for the parental melts and indicates that crustal contribution for magma diversification was not relevant. Sr and Nd isotope compositions together with major and trace element geochemistry point to the origin of the parental magmas by melting of a metasomatized mantle source, with garnet behaving as a residual phase, whilst phlogopite was an important contributor to the generated melts. Both geochemical features of Dehsalm porphyries and its association with Cu-Mo mineralization agree with a mature continental arc setting related to the convergence of Afghan and Lut plates during Oligocene. The data on the Dehsalm granitoids reveal a strong affinity with the contemporary rocks from Chah-Shaljami, studied in a previous work (Arjmandzadeh et al., 2011). Moreover, the wider range of compositions (including more mafic compositions) at Dehsalm provides additional support for the suggestion that parental magmas have a mantle origin. Acknowledgements This research was financially supported by the Geobiotec Research Unit (funded by the Portuguese Foundation for Science and Technology, through project PEst-C/CTE/UI4035/2011), University of Aveiro, Portugal. Ministry of Sciences, Research and Technology of Iran granted a sabbatical scholarship of R. Arjmandzadeh in Portugal References Arjmandzadeh, R., Karimpour, M.H., Mazaheri, S.A., Santos, J.F., Medina, J., Homam, S.M., 2011. Sr-Nd isotope geochemistry and petrogenesis of the Chah-Shaljami granitoids (Lut Block, Eastern Iran). Journal of Asian Earth Sciences 41: p. 283-296. Arjmandzadeh, R., Karimpour, M.H., Mazaheri, S.A., Santos, J.F., Medina, J., Homam, S.M., 2012. Petrogenesis, tectonomagmatic setting and mineralization potential of Dehsalm granitoids, Lut block, Eastern Iran. Journal of Earth Sciences, accepted.

Miocene Basaltic Lava Flows and Dikes of the Intervening Area Between Picture Gorge and Steens Basalt of the CRBG, Eastern Oregon

NASA Astrophysics Data System (ADS)

Cahoon, E. B.; Streck, M. J.

2016-12-01

Mid-Miocene basaltic lavas and dikes are exposed in the area between the southern extent of the Picture Gorge Basalt (PGB) and the northern extent of Steens Basalt in a wide corridor of the Malheur National Forest, eastern Oregon. An approximate mid-Miocene age of sampled basaltic units is indicated by stratigraphic relationships to the 16 Ma Dinner Creek Tuff. Lavas provide an opportunity to extend and/or revise distribution areas of either CRBG unit and explore the petrologic transition between them. The PGB and the Steens Basalt largely represent geochemically distinct tholeiitic units of the CRBG; although each unit displays internal complexity. Lavas of PGB are relatively primitive (MgO 5-9 wt.%) while Steens Basalt ranges in MgO from >9 to 3 wt.% but both units are commonly coarsely porphyritic. Conversely, Steens Basalt compositions are on average more enriched in highly incompatible elements (e.g. Rb, Th) and relatively enriched in the lesser incompatible elements (e.g. Y, Yb) compared to the Picture Gorge basalts. These compositional signatures produce inclined and flat patterns on mantle-normalized incompatible trace element plots but with similar troughs and spikes, respectively. New compositional data from our study area indicate basaltic lavas can be assigned as PGB lava flows and dikes, and also to a compositional group chemically distinct between Steens Basalt and PGB. Distribution of lava flows with PGB composition extend this CRBG unit significantly south/southeast closing the exposure gap between PGB and Steens Basalt. We await data that match Steens Basalt compositions but basaltic lavas with petrographic features akin to Steens Basalt have been identified in the study area. Lavas of the transitional unit share characteristics with Upper Steens and Picture Gorge basalt types, but identify a new seemingly unique composition. This composition is slightly more depleted in the lesser incompatible elements (i.e. steeper pattern) on mantle normalized incompatible element diagrams, relatively enriched in Sr, and overall reflects more HFSE depletion than Upper Steens Basalt. Similar compositional patterns have also been observed among lavas of the Strawberry Volcanics located immediately east of our study area.

Pyroxenite and peridotite xenoliths from Hexigten, Inner Mongolia: Insights into the Paleo-Asian Ocean subduction-related melt/fluid-peridotite interaction

NASA Astrophysics Data System (ADS)

Zou, Dongya; Liu, Yongsheng; Hu, Zhaochu; Gao, Shan; Zong, Keqing; Xu, Rong; Deng, Lixu; He, Detao; Gao, Changgui

2014-09-01

The in situ major, trace-element and Sr-isotopic compositions of the peridotite and pyroxenite xenoliths from the Hexigten region in the Xing-Meng orogenic belt (XMOB) were examined to evaluate the influences and contributions of the Paleo-Asian Oceanic slab subduction on the lithospheric mantle transformation. Pyroxenes in the Type 1 pyroxenite exhibit low and variable Mg# (67-85) and relatively high 87Sr/86Sr ratios (0.7036-0.7053), indicating that they were formed by assimilation and fractional crystallization processes during a basaltic underplating event. The peridotite and Type 2 pyroxenite xenoliths sampled the lithospheric mantle and recorded subduction-related metasomatism. The mineral chemistries of the Type 1 peridotite suggest that the lithospheric mantle beneath this area suffered 1-15% melt extraction. Clinopyroxene (Cpx) in some Type 1 peridotites are characterized by high (La/Yb)N coupled with marked depletions in high field strength elements (HFSE) (Nb, Ta, Zr, Hf and Ti) and negative correlations between the low Ti/Eu (Nb/La) and 87Sr/86Sr ratios (0.7037-0.7055), suggesting metasomatism by subduction-related CO2-rich fluids. Olivine (Ol) and orthopyroxene (Opx) in the Type 2 peridotite are characterized by a relatively low Mg# but high Ni contents. In addition to the normal incompatible element-depleted Opx, Opx with enrichments in Rb, Ba, Th, U, Nb, Ta and LREE were observed, as well. The Mg# of incompatible element-depleted Opx exhibits weak zonations (i.e., decreasing from the cores to the rims). Cpx and Opx of the Type 2 pyroxenite exhibit similarly high Mg# and Ni contents. Rb, Ba, Th, U, Nb, Ta and LREE contents and 87Sr/86Sr ratios of the Cpx increase from the cores to the rims. Moreover, Opx in the Type 2 peridotite and Cpx in the Type 2 pyroxenite exhibit increased Nb/Ta ratios and Ni contents relative to those in the Type 1 peridotites. These observations collectively suggest a rutile-bearing eclogite-derived silicic melt-peridotite reaction as the origin for the Type 2 peridotite and pyroxenite. Considering the geological setting, it is suggested that the melt/fluid-peridotite interactions were caused by the Paleo-Asian Ocean subduction, which could have contributed significantly to the transformation of the lithospheric mantle beneath the northern margin of the NCC, as well.

Early Earth differentiation [rapid communication

NASA Astrophysics Data System (ADS)

Walter, Michael J.; Trønnes, Reidar G.

2004-09-01

The birth and infancy of Earth was a time of profound differentiation involving massive internal reorganization into core, mantle and proto-crust, all within a few hundred million years of solar system formation ( t0). Physical and isotopic evidence indicate that the formation of iron-rich cores generally occurred very early in planetesimals, the building blocks of proto-Earth, within about 3 million years of t0. The final stages of terrestrial planetary accretion involved violent and tremendously energetic giant impacts among core-segregated Mercury- to Mars-sized objects and planetary embryos. As a consequence of impact heating, the early Earth was at times partially or wholly molten, increasing the likelihood for high-pressure and high-temperature equilibration among core- and mantle-forming materials. The Earth's silicate mantle harmoniously possesses abundance levels of the siderophile elements Ni and Co that can be reconciled by equilibration between iron alloy and silicate at conditions comparable to those expected for a deep magma ocean. Solidification of a deep magma ocean possibly involved crystal-melt segregation at high pressures, but subsequent convective stirring of the mantle could have largely erased nascent layering. However, primitive upper mantle rocks apparently have some nonchondritic major and trace element refractory lithophile element ratios that can be plausibly linked to early mantle differentiation of ultra-high-pressure mantle phases. The geochemical effects of crystal fractionation in a deep magma ocean are partly constrained by high-pressure experimentation. Comparison between compositional models for the primitive convecting mantle and bulk silicate Earth generally allows, and possibly favors, 10-15% total fractionation of a deep mantle assemblage comprised predominantly of Mg-perovskite and with minor but geochemically important amounts of Ca-perovskite and ferropericlase. Long-term isolation of such a crystal pile is generally consistent with isotopic constraints for time-integrated Sm/Nd and Lu/Hf ratios in the modern upper mantle and might account for the characteristics of some mantle isotope reservoirs. Although much remains to be learned about the earliest formative period in the Earth's development, a convergence of theoretical, physical, isotopic and geochemical arguments is beginning to yield a self-consistent portrait of the infant Earth.

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.

Across and along arc geochemical variations in altered volcanic rocks: Evidence from mineral chemistry of Jurassic lavas in northern Chile, and tectonic implications

NASA Astrophysics Data System (ADS)

Rossel, Pablo; Oliveros, Verónica; Ducea, Mihai N.; Hernandez, Laura

2015-12-01

Postmagmatic processes mask the original whole-rock chemistry of most Mesozoic igneous rocks from the Andean arc and back-arc units preserved in Chile. Mineral assemblages corresponding to subgreenschist metamorphic facies and/or propylitic hydrothermal alteration are ubiquitous in volcanic and plutonic rocks, suggesting element mobility at macroscopic and microscopic scale. However, fresh primary phenocrysts of clinopyroxene and plagioclase do occur in some of the altered rocks. We use major and trace element chemistry of such mineral phases to infer the geochemical variations of four Jurassic arc and four back-arc units from northern Chile. Clinopyroxene belonging to rocks of the main arc and two units of the bark-arc are augites with low contents of HFSE and REE; they originated from melting of an asthenospheric mantle source. Clinopyroxenes from a third back-arc unit show typical OIB affinities, with high Ti and trace element contents and low Si. Trace elemental variations in clinopyroxenes from these arc and back-arc units suggest that olivine and clinopyroxene were the main fractionating phases during early stages of magma evolution. The last back-arc unit shows a broad spectrum of clinopyroxene compositions that includes depleted arc-like augite, high Al and high Sr-Ca diopside (adakite-like signature). The origin of these lavas is the result of melting of a mixture of depleted mantle plus Sr-rich sediments and subsequent high pressure fractionation of garnet. Thermobarometric calculations suggest that the Jurassic arc and back-arc magmatism had at least one crustal stagnation level where crystallization and fractionation took place, located at ca. ~ 8-15 km. The depth of this stagnation level is consistent with lower-middle crust boundary in extensional settings. Crystallization conditions calculated for high Al diopsides suggest a deeper stagnation level that is not consistent with a thinned back-arc continental crust. Thus minor garnet fractionation occurred before these magmas reached the base of the crust. The presented data support the existence of a heterogeneous sub arc mantle and complex magmatic processes in the early stages of the Andean subduction.

Olivine and melt inclusion chemical constraints on the source of intracontinental basalts from the eastern North China Craton: Discrimination of contributions from the subducted Pacific slab

NASA Astrophysics Data System (ADS)

Li, Hong-Yan; Xu, Yi-Gang; Ryan, Jeffrey G.; Huang, Xiao-Long; Ren, Zhong-Yuan; Guo, Hua; Ning, Zhen-Guo

2016-04-01

Contributions from fluid and melt inputs from the subducting Pacific slab to the chemical makeup of intraplate basalts erupted on the eastern Eurasian continent have long been suggested but have not thus far been geochemically constrained. To attempt to address this question, we have investigated Cenozoic basaltic rocks from the western Shandong and Bohai Bay Basin, eastern North China Craton (NCC), which preserve coherent relationships among the chemistries of their melt inclusions, their hosting olivines and their bulk rock compositions. Three groups of samples are distinguished: (1) high-Si and (2) moderate-Si basalts (tholeiites, alkali basalts and basanites) which were erupted at ∼23-20 Ma, and (3) low-Si basalts (nephelinites) which were erupted at <9 Ma. The high-Si basalts have lower alkalies, CaO and FeOT contents, lower trace element concentrations, lower La/Yb, Sm/Yb and Ce/Pb but higher Ba/Th ratios, and lower εNd and εHf values than the low-Si basalts. The olivines in the high-Si basalts have higher Ni and lower Mn and Ca at a given Fo value than those crystallizing from peridotite melts, and their corresponding melt inclusions have lower CaO contents than peridotite melts, suggesting a garnet pyroxenitic source. The magmatic olivines from low-Si basalts have lower Ni but higher Mn at a given Fo value than that of the high-Si basalts, suggesting more olivine in its source. The olivine-hosted melt inclusions of the low-Si basalts have major elemental signatures different from melts of normal peridotitic or garnet pyroxenitic mantle sources, pointing to their derivation from a carbonated mantle source consisting of peridotite and garnet pyroxenite. We propose a model involving the differential melting of a subduction-modified mantle source to account for the generation of these three suites of basalts. Asthenospheric mantle beneath the eastern NCC, which entrains garnet pyroxenite with an EM1 isotopic signature, was metasomatized by carbonatitic melts from carbonated eclogite derived from subducted Pacific slab materials present in the deeper mantle. High degree melting of garnet pyroxenites from a shallower mantle source produced the early (∼23-20 Ma) higher-Si basalts. Mixing of these materials with deeper-sourced melts of carbonated mantle source produced the moderate-Si basalts. A thicker lithosphere after 9 Ma precluded melting of shallower garnet pyroxenites, so melts of the deeper carbonated mantle source are responsible for the low-Si basalts.

Enrichment of 18O in the mantle sources of the Antarctic portion of the Karoo large igneous province

NASA Astrophysics Data System (ADS)

Heinonen, Jussi S.; Luttinen, Arto V.; Whitehouse, Martin J.

2018-03-01

Karoo continental flood basalt (CFB) province is known for its highly variable trace element and isotopic composition, often attributed to the involvement of continental lithospheric sources. Here, we report oxygen isotopic compositions measured with secondary ion mass spectrometry for hand-picked olivine phenocrysts from 190 to 180 Ma CFBs and intrusive rocks from Vestfjella, western Dronning Maud Land, that form an Antarctic extension of the Karoo province. The Vestfjella lavas exhibit heterogeneous trace element and radiogenic isotope compositions (e.g., ɛ Nd from - 16 to + 2 at 180 Ma) and the involvement of continental lithospheric mantle and/or crust in their petrogenesis has previously been suggested. Importantly, our sample set also includes rare primitive dikes that have been derived from depleted asthenospheric mantle sources ( ɛ Nd up to + 8 at 180 Ma). The majority of the oxygen isotopic compositions of the olivines from these dike rocks (δ18O = 4.4-5.2‰; Fo = 78-92 mol%) are also compatible with such sources. The olivine phenocrysts in the lavas, however, are characterized by notably higher δ18O (6.2-7.5‰; Fo = 70-88 mol%); and one of the dike samples gives intermediate compositions (5.2‒6.1‰, Fo = 83-87 mol%) between the other dikes and the CFBs. The oxygen isotopic compositions do not correlate with radiogenic isotope compositions susceptible to crustal assimilation (Sr, Nd, and Pb) or with geochemical indicators of pyroxene-rich mantle sources. Instead, δ18O correlates positively with enrichments in large-ion lithophile elements (especially K) and 187Os. We suggest that the oxygen isotopic compositions of the Vestfjella CFB olivines primarily record large-scale subduction-related metasomatism of the sub-Gondwanan mantle (base of the lithosphere or deeper) prior to Karoo magmatism. The overall influence of such sources to Karoo magmatism is not known, but, in addition to continental lithosphere, they may be responsible for some of the geochemical heterogeneity observed in the CFBs.

Geochemical Constraints on the Size of the Moon-Forming Giant Impact

NASA Astrophysics Data System (ADS)

Piet, Hélène; Badro, James; Gillet, Philippe

2017-12-01

Recent models involving the Moon-forming giant impact hypothesis have managed to reproduce the striking isotopic similarity between the two bodies, albeit using two extreme models: one involves a high-energy small impactor that makes the Moon out of Earth's proto-mantle; the other supposes a gigantic collision between two half-Earths creating the Earth-Moon system from both bodies. Here we modeled the geochemical influence of the giant impact on Earth's mantle and found that impactors larger than 15% of Earth mass result in mantles always violating the present-day concentrations of four refractory moderately siderophile trace elements (Ni, Co, Cr, and V). In the aftermath of the impact, our models cannot further discriminate between a fully and a partially molten bulk silicate Earth. Then, the preservation of primordial geochemical reservoirs predating the Moon remains the sole argument against a fully molten mantle after the Moon-forming impact.

Petrogenesis of Near-Ridge Seamounts: AN Investigation of Mantle Source Heterogeneity and Melting Processes

NASA Astrophysics Data System (ADS)

Baxter, N. L.; Perfit, M. R.; Lundstrom, C.; Clague, D. A.

2010-12-01

Near-ridge (NR) seamounts offer an important opportunity to study lavas that have similar sources to ridge basalts but have been less affected by fractionation and homogenization that takes place at adjacent spreading ridge axes. By studying lavas erupted at these off-axis sites, we have the potential to better understand source heterogeneity and melting and transport processes that can be applied to the ridge system as a whole. One purpose of our study is to investigate the role of dunite conduits in the formation of near-ridge seamount chains. We believe that near-ridge seamounts could form due to focusing of melts in dunite channels located slightly off-axis and that such conduits may be important in the formation and transport of melt both on- and off-axis (Lundstrom et al., 2000). New trace element and isotopic analyses of glasses from Rogue, Hacksaw, and T461 seamounts near the Juan de Fuca Ridge (JdFR), the Lamont Seamounts adjacent to the East Pacific Rise (EPR) ~ 10°N, and the Vance Seamounts next to the JdFR ~45°N provide a better understanding of the petrogenesis of NR seamounts. Our data indicate that lavas from these seamounts have diverse incompatible trace element compositions that range from highly depleted to slightly enriched in comparison to associated ridge basalts. Vance A lavas (the oldest in the Vance chain) have the most enriched signatures and lavas from Rogue seamount on the JdFR plate have the most depleted signatures. Sr-Nd-Pb isotopic ratios indicate that NR seamount lava compositions vary within the chains as well as within individual seamounts, and that there is some mixing between heterogeneous, small-scale mantle sources. Using the program PRIMELT2.XLS (Herzberg and Asimow, 2008), we calculated mantle potential temperatures (Tp) for some of the most primitive basalts erupted at these seamounts. Our data indicate that NR seamount lavas have Tp values that are only slightly higher than that of average ambient mantle. Variations in major and trace elements along with geochemical modeling suggest a heterogeneous mantle source that melts to different extents. Shallow level crystal fractionation and mixing cannot explain the geochemical diversity found at NR seamounts. We are using the modeling programs MELTS (Ghiorso et al., 2002) and IRIDIUM (Boudreau, 2003) to model processes hypothesized to form dunite conduits (dissolution of pyroxenes and precipitation of olivine), to evaluate if these dissolution/precipitation processes can produce some of the geochemical diversity observed at these seamounts.

Restitic or not? Insights from trace element content and crystal - Structure of spinels in African mantle xenoliths

NASA Astrophysics Data System (ADS)

Lenaz, Davide; Musco, Maria Elena; Petrelli, Maurizio; Caldeira, Rita; De Min, Angelo; Marzoli, Andrea; Mata, Joao; Perugini, Diego; Princivalle, Francesco; Boumehdi, Moulay Ahmed; Bensaid, Idris Ali Ahmadi; Youbi, Nasrrddine

2017-05-01

The lithospheric architecture of Africa consists of several Archean cratons and smaller cratonic fragments, stitched together and flanked by polycyclic fold belts. Here we investigate the structure and chemistry of spinels from lithospheric mantle xenoliths from distinct tectonic settings, i.e. from the Saharan metacraton in Libya (Waw-En-Namus) which could show archaic chemical features, Cameroon (Barombi Koto and Nyos Lakes) where the Sub Continental Lithospheric Mantle was modified during the Pan-African event and fluxed by asthenospheric melts of the Tertiary Cameroon Volcanic Line and Morocco (Tafraoute, Bou-Ibalrhatene maars) in the Middle Atlas where different metasomatic events have been recorded. From a structural point of view it is to notice that the Libyan spinels can be divided into two groups having different oxygen positional parameter (u > 0.2632 and u < 0.2627, respectively), while those from Cameroon are in between those values as the Moroccan ones already studied by other authors. The intracrystalline closure temperature (Tc) of the here studied spinels is different among the different samples with one Libyan group (LB I) showing Tc in the range 490-640 °C and the other 680-950 °C (LB II). Cameroon and Morocco spinels show a Tc in the range 630-760 °C. About 150 different spinels have been studied for their trace element content and it can be seen that many of them are related to Cr content, while Zn and Co are not and clearly distinguish the occurrences. Differences in the trace element chemistry, in the structural parameters and in the intracrystalline closure temperatures suggest that a different history should be considered for Cameroon, Morocco and LB I and LB II spinels. Even if it was not considered for this purpose, we tentatively used the Fe2 +/Fe3 + vs. TiO2 diagram that discriminate between peridotitic and the so-called "magmatic" spinels, i.e. spinel crystallized from melts. LB I and LB II spinels plot in the peridotitic field while Cameroon and Morocco spinels fall in the magmatic one. Consequently, the xenoliths sampled from a probably juvenile SCLM at the edge of the most important lithospheric roots (i.e. Cameroon and Morocco) apparently have spinels possibly fractionated in situ from percolating melts and do not represent a real spinel-peridotite facies. On the contrary mantle xenoliths from Libya exhibit spinels with peridotitic features compatible with a slow ascent of a mantle diapir (plume).

Assessing δ18O heterogeneity in Icelandic olivine crystals

NASA Astrophysics Data System (ADS)

Bar Rasmussen, M.; Halldorsson, S. A.; Martin, W.; Gibson, S. A.; Hilton, D. R.

2017-12-01

δ18O systematics of Icelandic basalts are notably distinct from MORB-sourced basalts. This difference has previously been attributed to interaction with low δ18O meteoric water in the crust or slight heterogeneity within the Icelandic mantle [1]. Studies addressing this issue have mostly involved batch mineral laser-fluorination analysis which cannot resolve any intra-mineral δ18O variability that might be present due to shallow-level processes, e.g. crustal contamination [2]. We present a study of olivine crystals found in basalts covering the neovolcanic rift and flank zones as well as older Tertiary crust, in which we couple in-situ δ18O-measurements with major and trace elements using SIMS, high-precision EMP and LA ICP-MS. Most samples have previously been analysed for 3He/4He which ranges from 6.7 to 47.8 RA, the largest span reported for any oceanic island [3]. Our analysed olivine grains, range in Fo# between 79.9 to 91.8 with limited intra-grain variability. Independent of Fo#, we observe a variation in δ18O(Ol) of >3 ‰ across Iceland, with most crystals plotting below the expected depleted mantle-value ( 5.1 ± 0.2‰ [4]). The lowest δ18O(Ol) of +2.77 ‰, is found in crystals with Fo# 86 from central Iceland, closest to the inferred plume head [3]. Trace element ratios for these olivine grains (e.g. Zn/Fe) strongly indicate a peridotitic mantle source, which implies a shallow (likely crustal) origin of low δ18O(Ol) for this region. In contrast, olivine crystals from the South Iceland Volcanic Zone (a region of active rift propagation and transitional to alkalic volcanism) display trace element ratios that are indicative of a greater amount of pyroxenite in their melt source region. The δ18O(Ol) of these samples vary significantly (from +3.45 to +4.98 ‰) which, together with their elevated 3He/4He values, implies entrainment of a lower δ18O mantle-source by a less-degassed mantle plume source. Further modelling will be performed to evaluate the role of crustal-level processes in generating the low δ18O values. [1] Muehlenbachs et al., (1974), GCA 38, 677-588 [2] Bindemann et al., (2008), GCA 72, 4397-4420 [3] Harðardóttir et al., (2017), in press [4] Eiler, (2001), RMG, 43, 319-364

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.

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.

Multielement extraction system for the determination of 18 trace elements in geochemical samples

USGS Publications Warehouse

Clark, J.R.; Viets, J.G.

1981-01-01

A Methyl isobutyl ketone-Amine synerGistic Iodide Complex (MAGIC) extraction system has been developed for use in geochemical exploration which separates a maximum number of trace elements from interfering matrices. Extraction curves for 18 of these trace elements are presented: Pd, Pt, Cu, Ag, Au, Zn, Cd, Hg, Ga, In, Tl, Sa, Pb, As, Sb, Bi, Se, and Te. The acid normality of the aqueous phase controls the extraction into the organic phase, and each of these 18 elements has a broad range of HCl normality over which H is quantitatively extracted, making H possible to determine all 18 trace elements from a single sample digestion or leach solution. The extract can be analyzed directly by flame atomic absorption or inductively coupled plasma emission spectroscopy. Most of these 18 elements can be determined by Nameless atomic absorption after special treatment of the organic extract.

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.

Geochemical constraints on the spatial distribution of recycled oceanic crust in the mantle source of late Cenozoic basalts, Vietnam

NASA Astrophysics Data System (ADS)

Hoang, Thi Hong Anh; Choi, Sung Hi; Yu, Yongjae; Pham, Trung Hieu; Nguyen, Kim Hoang; Ryu, Jong-Sik

2018-01-01

This study presents a comprehensive analysis of the major and trace element, mineral, and Sr, Nd, Pb and Mg isotopic compositions of late Cenozoic intraplate basaltic rocks from central and southern Vietnam. The Sr, Nd, and Pb isotopic compositions of these basalts define a tight linear array between Indian mid-ocean-ridge basalt (MORB)-like mantle and enriched mantle type 2 (EM2) components. These basaltic rocks contain low concentrations of CaO (6.4-9.7 wt%) and have high Fe/Mn ratios (> 60) and FeO/CaO-3MgO/SiO2 values (> 0.54), similar to partial melts derived from pyroxenite/eclogite sources. This similarity is also supported by the composition of olivine within these samples, which contains low concentration of Ca and high concentrations of Ni, and shows high Fe/Mn ratios. The basaltic rocks have elevated Dy/Yb ratios that fall within the range of melts derived from garnet lherzolite material, although their Yb contents are much higher than those of modeled melts derived from only garnet lherzolite material and instead plot near the modeled composition of eclogite-derived melts. The Vietnamese basaltic rocks have lighter δ26Mg values (- 0.38 ± 0.06‰) than is expected for the normal mantle (- 0.25 ± 0.07‰), and these values decrease with decreasing Hf/Hf* and Ti/Ti* ratios, indicating that these basalts were derived from a source containing carbonate material. On primitive mantle-normalized multi-element variation diagrams, the central Vietnamese basalts are characterized by positive Sr, Eu, and Ba anomalies. These basalts also plot within the pelagic sediment field in Pbsbnd Pb isotopic space. This suggests that the mantle source of the basalts contained both garnet peridotite and recycled oceanic crust. A systematic analysis of variations in geochemical composition in basalts from southern to central Vietnam indicates that the recycled oceanic crust (possibly the paleo-Pacific slab) source material contains varying proportions of gabbro, basalt, and sediment. The basalts from south-central Vietnam (12°N-14°N) may be dominated by the lowest portion of the residual slab that contains rutile-bearing plagioclase-rich gabbroic eclogite, whereas the uppermost portion of the recycled slab, including sediment and basaltic material with small amounts of gabbro, may be a major constituent of the source for the basalts within the central region of Vietnam (14°N-16°N). Finally, the southern region (10°N-12°N) contains basalts sourced mainly from recycled upper oceanic crust that is basalt-rich and contains little or no sediment.

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

Peridotite xenoliths from the Polynesian Austral and Samoa hotspots: Implications for the destruction of ancient 187Os and 142Nd isotopic domains and the preservation of Hadean 129Xe in the modern convecting mantle

NASA Astrophysics Data System (ADS)

Jackson, M. G.; Shirey, S. B.; Hauri, E. H.; Kurz, M. D.; Rizo, H.

2016-07-01

The Re-Os systematics in 13 peridotite xenoliths hosted in young (<0.39 myr) rejuvenated lavas from the Samoan island of Savai'i and 8 peridotite xenoliths from 6 to 10 myr old lavas from the Austral island of Tubuai have been examined to evaluate the history of the oceanic mantle in this region. Modal mineralogy, trace element compositions and 187Os/188Os ratios suggest that these peridotites are not cognate or residual to mantle plumes but rather samples of Pacific oceanic lithosphere created at the ridge. Savai'i and Tubuai islands lie along a flow line in the Pacific plate, and provide two snapshots (separated by over 40 Ma in time) of Pacific mantle that originated in the same region of the East Pacific rise. Tubuai xenoliths exhibit 187Os/188Os from 0.1163 to 0.1304, and Savai'i (Samoa) xenoliths span a smaller range from 0.1173 to 0.1284. The 187Os/188Os ratios measured in Tubuai xenoliths are lower than (and show no overlap with) basalts from Tubuai. The 187Os/188Os of the Savai'i xenoliths overlap the isotopic compositions of lavas from the island of Savai'i, but also extend to lower 187Os/188Os than the lavas. 3He/4He measurements of a subset of the xenoliths range from 2.5 to 6.4 Ra for Tubuai and 10.8 to 12.4 Ra for Savai'i. Like abyssal peridotites and xenoliths from oceanic hotspots that sample the convecting mantle, Os isotopes from the Savai'i and Tubuai xenolith suites are relatively unradiogenic, but do not preserve a record of depleted early-formed (Hadean and Archean) mantle domains expected from earlier cycles of ridge-related depletion, continent extraction, or subcontinental lithospheric mantle erosion. The lack of preservation of early-formed, geochemically-depleted Os-isotopic and 142Nd/144Nd domains in the modern convecting mantle contrasts with the preservation of early-formed (early-Hadean) 129Xe/130Xe isotopic heterogeneities in the convecting mantle. This can be explained if the initial isotopic signatures in Re-Os and Sm-Nd systems are erased by recycling because the parent and daughter elements are retained in subducting slabs and more efficiently returned to the mantle during subduction than Xe. In this way, early-formed Os and Nd-isotopic heterogeneities could have been overprinted with, and diluted by, younger isotopic signatures. In contrast, preservation of early-formed heterogeneities in the modern convecting mantle is possible for other elements, such as Xe, that are not as efficiently recycled back into the mantle, owing to greater fluid mobility that concentrates such elements in the near-surface. Differing recycling efficiencies for Os, Nd and Xe lead to wide differences in the preservation of Hadean isotopic signatures of these elements in the modern convecting mantle. In general, incompatible elements that are fluid mobile (e.g., Xe) concentrate in surface reservoirs and are more likely to preserve Hadean geochemical signatures in the convecting mantle than compatible elements (e.g., Os) and fluid immobile incompatible elements (e.g., Nd).

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.

Geochemistry of ocean floor serpentinites world-wide: constraints on the ultramafic input to subduction zones

NASA Astrophysics Data System (ADS)

Kodolányi, J.; Pettke, T.; Spandler, C.; Kamber, B.; Gméling, K.

2009-04-01

Serpentinite can be a major component of the upper part of the oceanic lithosphere and is a significant H2O-contributor to subduction zones (Scambelluri et al. 2004). Serpentinite dehydration releases large amounts of water through a very limited number of discontinuous reactions and it is therefore expected to have the potential of leaving a trace element chemical fingerprint in overlying rocks (Ulmer and Trommsdorff 1995; Scambelluri et al. 2004; see also Pettke et al. 2009). We present major and trace element whole rock (XRF, ICP-MS and PGAA) and in-situ mineral (EPMA and LA-ICP-MS) analyses of serpentinized peridotites sampled on DSDP/ODP drilling cruises, in order to chemically characterize the hydrated ultramafic input of subduction zones. The studied 39 samples cover all major geodynamic settings where serpentinites occur on recent ocean floors (fast and slow spreading mid-ocean ridges, passive margins and supra-subduction zones). All rock samples consist of one or two serpentine (srp) polymorphs, brucite (brc), magnetite (mag), and relic high-temperature mantle minerals: olivine (ol), orthopyroxene (opx), clinopyroxene (cpx) and spinel (spl). Serpentine + brc replace ol, forming a mesh-like network around relic crystal fragments. Magnetite usually forms strings of individual crystals along the srp mesh-network. Very rare iowaite (a H2O and Cl-bearing Fe-Mg oxy-hydroxide) remnants were found around the ol core of mesh srp and in the srp ± brc replacements after ol mesh cores. Orthopyroxene alters to bastitic pseudomorphs which consist of srp rarely accompanied by brc. Associated mag is generally absent. The degree of ol and opx alteration is variable, i.e., there are samples in which opx is completely whereas ol is only partially altered and vice versa, which suggests variable temperatures of alteration (alteration rate of opx is higher than that of ol above ca. 350 °C; Martin and Fyfe 1970). Clinopyroxene and spl appear to be weakly altered in thoroughly serpentinized samples. Where present, carbonate (cab) forms veins or fills former srp ± brc pseudomorphs after ol or opx. Major, minor and trace element chemistry of the serpentinites generally reflects that of their ultramafic precursor (Mg-rich and Si-poor rocks with low trace element contents). With respect to certain elements, however, we detect significant serpentinization-related changes. Besides their high H2O-contents (8.7-17.2 wt. %), the hydrated harzburgites and lherzolites also display high B and Cl concentrations (8-177 μg/g and 1160-5920 μg/g, respectively) relative to depleted mantle values (0.06 and 0.51 ppm, respectively; Salters and Stracke 2004). Supra-subduction zone serpentinites contain 10 to 100 times more Cs (0.04-1.2 μg/g) and Rb (0.1-7.1 μg/g) than samples from mid-ocean ridges and passive margins (Cs: below 0.07 μg/g; Rb: 0.004-1.17 μg/g). We often observe 100 to 1000-fold enrichments in U, Pb, Sr and Li relative to elements of similar compatibility in the mantle. In-situ mineral analyses suggest that B and Cl reside in serpentine minerals. Cesium and Rb whole rock and mineral chemical data correlate well, too. If carbonates are not present, the Sr budget of serpentinites is largely controlled by serpentine minerals that take up 0.36 to 21 μg/g Sr, i.e., orders of magnitude more than concentrations of precursor ol and opx. Bastites tend to have (about 1.5-4 times) higher trace-element concentrations than mesh rims, suggesting that precursor mineralogy (e.g. harzburgites vs. dunites) and alteration temperature (Martin and Fyfe 1970) can affect serpentinite chemistry. Enrichments of U, Pb and Li may have multiple origins, i.e., may be only partly related to serpentinization and low-temperature carbonate addition. Our study shows that serpentinites from representative geodynamic settings have variable, but generally depleted chemical character, inherited from precursor mantle rocks. However, notably B and Cl are enriched, but not uniformly so and independent of geodynamic setting. Supra-subduction zone serpentinites reveal additional enrichments in Cs, Rb, ±Sr, identifying an alteration fluid source that is not pure seawater. In conclusion, precursor mineralogy and magmatic history together with hydration temperature govern the trace element budget of ocean floor serpentinites, which, apart from supplying H2O to the subduction zone, may also be a significant source of B and Cl to the arc magma source and, depending on geodynamic setting, may even influence the element budget for Cs, Rb, Pb, U and .Sr. References: Martin B, Fyfe WS (1970) Some experimental and theoretical observations on the kinetics of hydration reactions with particular reference to serpentinization. Chem Geol 6: 185-202 Pettke T, Spandler C, Kodolányi J, Scambelluri M (2009) The chemical signatures of progressive dehydration stages in subducted serpentinites (this volume) Salters VJM, Stracke A (2004) Composition of the depleted mantle. Geochem Geophys Geosyst 5 Doi: 10.1029/2003GC000597 Scambelluri M, Fiebig J, Malaspina N, Müntener O, Pettke T (2004) Serpentinite Subduction: Implications for Fluid Processes and Trace-Element Recycling. Int Geol Rev 46: 595-613 Ulmer P, Trommsdorff V (1995) Serpentine stability to mantle depths and subduction-related magmatism. Science 268: 858-861

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.

Sediment-peridotite interactions in a thermal gradient: mineralogic and geochemical effects and the "sedimentary signature" of arc magmas

NASA Astrophysics Data System (ADS)

Woodland, Alan; Girnis, Andrei; Bulatov, Vadim; Brey, Gerhard; Höfer, Heidi; Gerdes, Axel

2017-04-01

Strong thermal and chemical gradients are characteristic of the slab-mantle interface in subduction zones where relatively cold sediments become juxtaposed with hotter peridotite of the mantle wedge. The formation of arc magmas is directly related to mass transfer processes under these conditions. We have undertaken a series of experiments to simulate interactions and mass transfer at the slab-mantle interface. In addition to having juxtaposed sediment and peridotite layers, the experiments were performed under different thermal gradients. The sediment had a composition similar to GLOSS (1) and also served as the source of H2O, CO2 and a large selection of trace elements. The peridotite was a depleted garnet harzburgite formed from a mixture of natural hand-picked olivine, opx and garnet. Graphite was added to this mixture to establish a redox gradient between the two layers. Experiments were performed at 7.5-10 GPa to simulate the processes during deep subduction. The thermal gradient was achieved by displacing the sample capsule (Re-lined Pt) from the center of the pressure cell. The gradient was monitored with separate thermocouples at each end of the capsule and by subsequent opx-garnet thermometry across the sample. Maximum temperatures varied from 1400˚ -900˚ C and gradients ranged from 200˚ -800˚ C. Thus, in some experiments melting occurred in the sediment layer and in others this layer remained subsolidus, only devolatilizing. Major and trace elements were transported both in the direction of melt percolation to the hot zone, as well as down temperature. This leads to the development of zones with discrete phase assemblages. Olivine in the peridotite layer becomes converted to orthopyroxene, which is due to Si addition, but also migration of Mg and Fe towards the sediment. In the coldest part of a sample, the sediment is converted into an eclogitic cpx + garnet assemblage. A thin zone depleted in almost all trace elements is formed in peridotite directly above the sediment/peridotite boundary and defines the region of maximum metasomatic alteration. With a low Tmin, fluid-mobile Ba, Rb, Sr and Li are more strongly transported into the melt zone compared to HFSE and REE. At Tmin > 700˚ C, all incompatible elements are extracted from the solid into the melt. However, the mineral assemblage controls which elements are held back in the solid residue (i.e. MREE, HREE, Y, Sc, and to a lesser extent Ti, Zr and Hf in garnet). Peridotite-sediment interaction can produce humite-group minerals, particularly in the presence of F. Negative Nb-Ta anomalies are caused by rutile and/or humite phases. Transport of melt or fluid from the sediment to the overlying mantle wedge produces metasomatized magma sources from which basaltic melts with sedimentary geochemical signatures can be derived. Adding even 1% of melt or fluid to depleted mantle peridotite is sufficient to produce basaltic melts with incompatible element contents similar to those observed in natural subduction-related magmas. Such signatures are retained at 6.5 and even 10 GPa when Tmin < 700˚ C. Plank, T., Langmuir C., 1998. Chem. Geol. 145, 325-394.

Separation of supercritical slab-fluids to form aqueous fluid and melt components in subduction zone magmatism.

PubMed

Kawamoto, Tatsuhiko; Kanzaki, Masami; Mibe, Kenji; Matsukage, Kyoko N; Ono, Shigeaki

2012-11-13

Subduction-zone magmatism is triggered by the addition of H(2)O-rich slab-derived components: aqueous fluid, hydrous partial melts, or supercritical fluids from the subducting slab. Geochemical analyses of island arc basalts suggest two slab-derived signatures of a melt and a fluid. These two liquids unite to a supercritical fluid under pressure and temperature conditions beyond a critical endpoint. We ascertain critical endpoints between aqueous fluids and sediment or high-Mg andesite (HMA) melts located, respectively, at 83-km and 92-km depths by using an in situ observation technique. These depths are within the mantle wedge underlying volcanic fronts, which are formed 90 to 200 km above subducting slabs. These data suggest that sediment-derived supercritical fluids, which are fed to the mantle wedge from the subducting slab, react with mantle peridotite to form HMA supercritical fluids. Such HMA supercritical fluids separate into aqueous fluids and HMA melts at 92 km depth during ascent. The aqueous fluids are fluxed into the asthenospheric mantle to form arc basalts, which are locally associated with HMAs in hot subduction zones. The separated HMA melts retain their composition in limited equilibrium with the surrounding mantle. Alternatively, they equilibrate with the surrounding mantle and change the major element chemistry to basaltic composition. However, trace element signatures of sediment-derived supercritical fluids remain more in the melt-derived magma than in the fluid-induced magma, which inherits only fluid-mobile elements from the sediment-derived supercritical fluids. Separation of slab-derived supercritical fluids into melts and aqueous fluids can elucidate the two slab-derived components observed in subduction zone magma chemistry.

Separation of supercritical slab-fluids to form aqueous fluid and melt components in subduction zone magmatism

PubMed Central

Kawamoto, Tatsuhiko; Kanzaki, Masami; Mibe, Kenji; Ono, Shigeaki

2012-01-01

Subduction-zone magmatism is triggered by the addition of H2O-rich slab-derived components: aqueous fluid, hydrous partial melts, or supercritical fluids from the subducting slab. Geochemical analyses of island arc basalts suggest two slab-derived signatures of a melt and a fluid. These two liquids unite to a supercritical fluid under pressure and temperature conditions beyond a critical endpoint. We ascertain critical endpoints between aqueous fluids and sediment or high-Mg andesite (HMA) melts located, respectively, at 83-km and 92-km depths by using an in situ observation technique. These depths are within the mantle wedge underlying volcanic fronts, which are formed 90 to 200 km above subducting slabs. These data suggest that sediment-derived supercritical fluids, which are fed to the mantle wedge from the subducting slab, react with mantle peridotite to form HMA supercritical fluids. Such HMA supercritical fluids separate into aqueous fluids and HMA melts at 92 km depth during ascent. The aqueous fluids are fluxed into the asthenospheric mantle to form arc basalts, which are locally associated with HMAs in hot subduction zones. The separated HMA melts retain their composition in limited equilibrium with the surrounding mantle. Alternatively, they equilibrate with the surrounding mantle and change the major element chemistry to basaltic composition. However, trace element signatures of sediment-derived supercritical fluids remain more in the melt-derived magma than in the fluid-induced magma, which inherits only fluid-mobile elements from the sediment-derived supercritical fluids. Separation of slab-derived supercritical fluids into melts and aqueous fluids can elucidate the two slab-derived components observed in subduction zone magma chemistry. PMID:23112158

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.

Melt Heterogeneity and Degassing at MT Etna from Melt Inclusions

NASA Astrophysics Data System (ADS)

Salem, L. C.; Edmonds, M.; Maclennan, J.; Corsaro, R. A.

2014-12-01

The melts feeding Mt Etna, Italy, are rich in volatiles and drive long-lasting powerful eruptions of basaltic magma in both effusive and explosive styles of activity. The volatile systematics of the volcanic system are well understood through melt inclusion and volcanic gas studies. Etna's melts are generated from a complex mantle setting, with subduction-related chemical modifications as well as OIB-type features, and then the melts must travel through thick carbonate-rich crust. The continual influx of mantle-derived volatile-rich magma controls the major compositional and eruptive features of Mount Etna and magma mixing has been recognized as an important process driving large eruptions [Kamenetsky, 2007]. Our study focusses on the 1669 eruption, the largest in historical times. Olivine-hosted melt inclusions were analyzed for volatile, trace and major elements using electron microprobe and ion probe (SIMS). We use volatile systematics and geochemical data to deconvolve mantle-derived heterogeneity from melt mixing and crystal fractionation. Our data are well described by a mixing trend between two distinct melts: a CO2-rich (CO2~1000ppm), incompatible trace element depleted melt (La/Yb~16), and a CO2-poor, enriched melt. The mixing also generates a strong correlation between Sr and CO2 in the melt inclusions dataset, reflecting the presence of a strong Sr anomaly in one of the end-member melts. We investigate the origin of this Sr anomaly by considering plagioclase dissolution and crustal assimilation. We also investigate degassing processes in the crust and plumbing system of the volcano. We compare our results with similar studies of OIB and arc-related basalts elsewhere and assess the implications for linking eruption size and style with the nature of the mantle-derived melts. Kamenetsky et al. (2007) Geology 35, 255-258.

Magmatic Processes at Kilauea Volcano Revealed by the Puu Oo Eruption

NASA Astrophysics Data System (ADS)

Garcia, M. O.; Marske, J. P.; Pietruszka, A. P.; Rhodes, J. M.; Norman, M. D.; Eiler, J.

2008-12-01

The ongoing Puu Oo eruption (1983 to present) provides an unprecedented opportunity to probe the crustal and mantle magmatic processes beneath Kilauea volcano. Here we present Pb, Sr, Nd and O isotope ratios, major- and trace-element abundances, olivine compositions, and petrography data for Puu Oo lavas an compare them to the Kilauea historical record. Crustal processes are dominated by olivine fractionation and accumulation with minor clinopyroxene fractionation, and to a lesser extent and only periodically when eruption rates decrease, by crustal contamination. Systematic variations in Sr isotope ratios, incompatible trace element ratios, and MgO-normalized major elements document remarkable changes in parental magma compositions delivered to Puu Oo. Inflections in some trends correlate broadly with increasing intermediate depth earthquakes under the Kilauea's summit and to changes in eruption rate. Thus, volcanic events are influenced by melting and transport processes. One surprising feature is the systematic trend of Puu Oo rock compositions away from and beyond typical historical Kilauea compositions towards those of lavas from neighboring Mauna Loa volcano. The source for this component in Puu Oo lavas is a hybrid with about equal mixtures of historical Kilauea and Mauna Loa end members. The Puu Oo lava trend continues the cyclic pattern of compositional variation that extends back over 1000 years. Similar trends are also recorded on a coarser scale in HSDP lavas. These patterns of cyclic compositional variation are important for understanding melting processes in Hawaiian and other volcanoes.

Evidence of Arc Magma Genesis in a Paleo-Mantle Wedge, the Higashi-Akaishi Peridotite, Japan

NASA Astrophysics Data System (ADS)

Till, C. B.; Guild, M. R.; Grove, T. L.; Carlson, R. W.

2014-12-01

Located in the Sanbagawa subduction-related high-pressure metamorphic belt in SW Japan on the island of Shikoku, the Higashi-akaishi peridotite body is composed of dunite, lherzolite and garnet clinopyroxenite, interfingered in one locality with quartz-rich eclogite. Previous work indicates the P-T history of the peridotite includes rapid prograde metamorphism with peak temperatures of 700-810°C and pressures of 2.9-3.8 GPa [1] at ~88-89 Ma followed by rapid exhumation at >2.5 cm/yr [2,3]. Major and trace element and isotopic data from samples within the Higashi-akaishi peridotite presented here and in another recent study [4] provide a record of subduction zone melting processes in a paleo-mantle wedge. Ultramafic samples range from 40-52 wt.% SiO2, 1-11 wt.% Al2O3 and 21-45 wt.% MgO with olivine and clinopyroxene Mg#'s as high as 0.93. The quartz-rich eclogite contains 62 wt.% SiO2, 6 wt.% MgO and 13 wt.% Al2O3 with trace element concentrations that are enriched relative to the ultramafic samples. 87Sr/86Sr (.703237-.704288), 143Nd/144Nd (ɛNd=+2 to +6) and Pb isotopic compositions are within the range of previously studied Japanese arc rocks. We interpret the pyroxenites as shallowly crystallized cumulates with varying amounts of trapped hydrous melt and the harzburgites as residues of melting. The peak P-T conditions of these rocks are similar to the solidus conditions of H2O-saturated fertile mantle near the base of the mantle wedge [5,6]. The presence of garnet porphyroblasts that enclose primary euhedral chlorite together with the chemical evidence, suggest these samples are associated with mantle melting in the presence of H2O. Major element modeling suggests the quartz-rich eclogite composition can be reproduced through mixing melts of subducted sediment with wet peridotite melts in the mantle wedge. Thus the Higashi-aikashi rock suite provides an in-situ record of the beginnings of hydrous melting and the mechanisms of metasomatism in the mantle wedge. [1] Enami et al. (2004) J. Meta. Geol. 22, 1-15. [2] Okamoto et al. (2004) Terra Nova 16, 81-89. [3] Wallis et al. (1990) J. Meta. Geol. 27, 93-105. [4] Hattori et al. (2010) Island Arc 19, 192-207. [5] Grove et al. (2006) Earth Planet. Sci. Lett. 249, 74-89. [6] Till et al. (2012) Cont. Min. Petrol. 163, 669-688.

Temporal constraints on magma generation and differentiation in a continental volcano: Buckland, eastern Australia

NASA Astrophysics Data System (ADS)

Crossingham, Tracey J.; Ubide, Teresa; Vasconcelos, Paulo M.; Knesel, Kurt M.; Mallmann, Guilherme

2018-03-01

The eastern margin of the Australian continent hosts a large number of Cenozoic intraplate volcanoes along a 2000 km long track. Here, we study mafic lavas from the Buckland volcano, Queensland, located in the northern (older) segment of this track, to assess magma generation and differentiation through time. The rocks are aphanitic to microporphyritic basalts, trachy-basalts and basanites. Incompatible element geochemistry together with Sr-Nd-Pb isotope ratios indicate that magmas formed from an enriched mantle I (EMI)-like garnet-bearing source with variable degrees of crustal contamination. Whole rock elemental variations suggest fractionation of olivine, plagioclase, clinopyroxene and/or magnetite. There is no petrographic or geochemical evidence of magma mixing in the studied rocks (e.g., lack of recycled minerals), suggesting a relatively quick ascent from the source to the surface without major storage at shallow levels. 40Ar/39Ar geochronology reveals two stages of volcanism: 30.3 ± 0.1 Ma and 27.4 ± 0.2 Ma. The Old Buckland (30.3 ± 0.1 Ma) melts have negative K anomalies, and incompatible element ratios suggest the occurrence of residual hydrous minerals in a metasomatised mantle source. We therefore infer that at the onset of volcanism, deep-mantle-derived magmas interacted with metasomatised sub-continental lithospheric mantle (SCLM). Major and trace element data, clinopyroxene thermobarometry and thermodynamic modelling indicate magma evolution by assimilation and fractional crystallisation (AFC) during ascent through the crust. Following a hiatus in volcanic activity of 2.5 Ma, eruption of Young Buckland (27.4 ± 0.2 Ma) lavas marked a shift towards more alkaline compositions. Trace element compositions indicate lower degrees of partial melting and a lack of interaction with metasomatic components. Young Buckland lavas become progressively more SiO2-saturated up stratigraphy, suggesting an increase in the degree of partial melting with time. Young Buckland lavas also have more radiogenic 87Sr/86Sr and 207Pb/204Pb ratios and less radiogenic 143Nd/144Nd ratios up stratigraphy. These isotopic variations, together with coupled increases in Pb and K and decreases in Ce/Pb (27.22 to 11.09) and Nb/U (68.30 to 29.96), suggest that crustal contamination also increased with time. By placing absolute age and stratigraphic constraints on the Buckland lavas, we have been able to ascertain differentiation signatures imposed on mantle-derived melts during ascent through the continental lithosphere over 3 Ma. Our study provides new constraints on magma generation and differentiation in continental intraplate volcanic systems.

Geochemical databases: minding the pitfalls to avoid the pratfalls

NASA Astrophysics Data System (ADS)

Goldstein, S. L.; Hofmann, A. W.

2011-12-01

The field of geochemistry has been revolutionized in recent years by the advent of databases (PetDB, GEOROC, NAVDAT, etc). A decade ago, a geochemical synthesis required major time investments in order to compile relatively small amounts of fragmented data from large numbers of publications, Now virtually all of the published data on nearly any solid Earth topic can be downloaded to nearly any desktop computer with a few mouse clicks. Most solid Earth talks at international meetings show data compilations from these databases. Applications of the data are playing an increasingly important role in shaping our thinking about the Earth. They have changed some fundamental ideas about the compositional structure of the Earth (for example, showing that the Earth's "trace element depleted upper mantle" is not so depleted in trace elements). This abundance of riches also poses new risks. Until recently, important details associated with data publication (adequate metadata and quality control information) were given low priority, even in major journals. The online databases preserve whatever has been published, irrespective of quality. "Bad data" arises from many causes, here are a few. Some are associated with sample processing, including incomplete dissolution of refractory trace minerals, or inhomogeneous powders, or contamination of key elements during preparation (for example, this was a problem for lead when gasoline was leaded, and for niobium when tungsten-carbide mills were used to powder samples). Poor analytical quality is a continual problem (for example, when elemental abundances are at near background levels for an analytical method). Errors in published data tables (more common than you think) become bad data in the databases. The accepted values of interlaboratory standards change with time, while the published data based on old values stay the same. Thus the pitfalls associated with the new data accessibility are dangerous in the hands of the inexperienced users (for example, a student of mine took the initiative to write a paper showing very creative insights, based on some neodymium isotope data on oceanic volcanics; unfortunately the uniqueness of the data reflected the normalization procedures used by different labs). Many syntheses assume random sampling even though we know that oversampled regions are over-represented. We will show examples where raw downloads of data from databases without extensive screening can yield data collections where the garbage swamps the useful information. We will also show impressive but meaningless correlations (e.g. upper-mantle temperature versus atmospheric temperature). In order to avoid the pratfalls, screening of database output is necessary. In order to generate better data consistency, new standards for reporting geochemical data are necessary.

Origin of the Mackenzie large igneous province and sourcing of flood basalts from layered intrusions

NASA Astrophysics Data System (ADS)

Day, J. M.; Pearson, D.

2013-12-01

The 1.27 Ga Coppermine continental flood basalt (CFB) in northern Canada represents the extrusive manifestation of the Mackenzie large igneous province (LIP) that includes the Mackenzie dyke swarm and the Muskox layered intrusion. New Re-Os isotope and highly siderophile element (HSE: Re, Pd, Pt, Ru, Ir, Os) abundance data are reported together with whole-rock major- and trace-element abundances and Nd isotopes to examine the behaviour of the HSE during magmatic differentiation and to place constraints on the extent of crustal interaction with mantle-derived melts. Mineral-chemical data are also reported for an unusual andesite glass flow (4.9 wt.% MgO) found in proximity to newly recognised picrites (>20 wt.% MgO) in the lowermost stratigraphy of the Coppermine CFB. Compositions of mineral phases in the andesite are similar to equivalent phases found in Muskox Intrusion chromitites and the melt composition is identical to Muskox chromite melt inclusions. Elevated HSE contents (e.g., 3.8 ppb Os) and the mantle-like initial Os isotope composition of this andesitic glass contrast strongly with oxygen isotope and lithophile element evidence for extensive crustal contamination. These signatures implicate an origin for the glass as a magma mingling product formed within the Muskox Intrusion during chromitite genesis. The combination of crust and mantle signatures define roles for both these reservoirs in chromitite genesis, but the HSE appear to be dominantly mantle-sourced. Combined with Nd isotope data that places the feeder for lower Coppermine CFB picrites and basalts within the Muskox Intrusion, this provides the strongest evidence yet for direct processing of some CFB within upper-crustal magma chambers. Modeling of absolute and relative HSE abundances in CFB reveal that HSE concentrations decrease with increasing fractionation for melts with <8×1 wt.% MgO in the Coppermine CFB, with picrites (>13.5wt.% MgO) from CFB having higher Os abundances than ocean island basalt (OIB) equivalents. The differences between CFB and OIB picrite absolute Os abundances may result from higher degrees of partial melting to form CFB but may also reflect incorporation of trace sulphide in CFB picrites from magmas that reached S-saturation in shallow-level magma chambers. Significant inter-element fractionation between (Re+Pt+Pd)/(Os+Ir+Ru) are generated during magmatic differentiation in response to strongly contrasting partitioning of these two groups of elements into sulphides and/or HSE-rich alloys. Furthermore, fractional crystallization has a greater role on absolute and relative HSE abundances than crustal contamination under conditions of CFB petrogenesis due to the dilution effect of continental crust. The Coppermine CFB define a Re-Os isochron with an age of 1263 +16/-20 Ma and initial gamma Os = +2.2×0.8. Combined data for the basaltic and intrusive portions of the Mackenzie LIP indicate a mantle source broadly within the range of the primitive upper mantle. The majority of Archaean komatiites and Phanerozoic CFB also require mantle sources with primitive upper mantle to chondritic Re/Os evolution, with exceptions typically being from analyses of highly-fractionated MgO-poor basalts.

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.

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.

Mantle to surface degassing of carbon- and sulphur-rich alkaline magma at El Hierro, Canary Islands

NASA Astrophysics Data System (ADS)

Longpré, Marc-Antoine; Stix, John; Klügel, Andreas; Shimizu, Nobumichi

2017-02-01

Basaltic volcanoes transfer volatiles from the mantle to the surface of the Earth. The quantification of deep volatile fluxes relies heavily on estimates of the volatile content of primitive magmas, the best archive of which is provided by melt inclusions. Available data from volcanoes producing mafic alkaline lavas in a range of tectonic settings suggest high volatile fluxes, but information remains sparse, particularly for intraplate ocean islands. Here we present measurements of volatile and trace element concentrations, as well as sulphur speciation, in olivine-hosted melt inclusions and matrix glasses from quenched basanite lava balloon samples from the 2011-2012 submarine eruption at El Hierro, Canary Islands. The results reveal remarkably high concentrations of dissolved volatiles and incompatible trace elements in this magma, with ∼80 ppm Nb and up to 3420 ppm CO2, 3.0 wt.% H2O and 5080 ppm S. Reconstructed primitive CO2 contents, considering CO2/Nb systematics and possible CO2 sequestration in shrinkage bubbles, reach weight percent levels, indicating that carbon is a major constituent of Canary Island magmas at depth and that exsolution of a CO2-rich fluid begins in the mantle at pressures in excess of 1 GPa. Correlations between sulphur concentration, sulphur speciation and water content suggest strong reduction of an initially oxidised mantle magma, likely controlled by coupled H2O and S degassing. This late-stage redox change may have triggered sulphide saturation, recorded by globular sulphide inclusions in clinopyroxene and ulvöspinel. The El Hierro basanite thus had a particularly high volatile-carrying capacity and released a minimum of 1.3-2.1 Tg CO2 and 1.8-2.9 Tg S to the environment, causing substantial stress on the local submarine ecosystem. These results highlight the important contribution of alkaline ocean island volcanoes, such as the Canary Islands, to volatile fluxes from the mantle.

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.

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.

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.

[Contents of macromineral and trace elements in spirulina (Arthrospira platensis) from France, Chad, Togo, Niger, Mali, Burkina-Faso and Central African Republic].

PubMed

Vicat, Jean-Paul; Doumnang Mbaigane, Jean-Claude; Bellion, Yves

2014-01-01

Data on mineral elements in spirulinas being limited, we analyzed macrominerals and trace elements of samples from France and Africa. Spirulinas cultivated in France have a composition in macromineral elements similar to those of the literature. The entire contents of trace elements are low. Unlike marine cyanobacteria, they do not concentrate rare-earth elements. Spirulina harvested in Chad has high levels in macrominerals and trace elements, due to traditional drying and harvesting methods. Rare-earth element levels are attributed to this pollution and not to their concentration in spirulinas, because rare-earth element normalized profiles of spirulina are strictly parallel to those of ouadis mud and very different from those of ouadis water. Despite the sometimes high content of total As, normal water consumption in Chad presents no health problems. Spirulinas grown in Togo, Niger, Mali, Burkina-Faso and Central African Republic have chemical compositions similar to those of Chad spirulinas, but with a lower content of macromineral and trace elements, reflecting a lower mineral pollution. Rare-earth element normalized patterns dismiss an aeolian pollution and the pollution is rather of pedological origin. They show no toxicity problem except spirulinas from Burkina-Faso, whose Pb content is too high. The variability of composition of spirulinas can be largely attributed to the mineral pollution of the samples. Significant levels of rare-earth elements sometimes found in the literature reflect this pollution. Copyright © 2013 Académie des sciences. Published by Elsevier SAS. All rights reserved.

A tale of phenocrysts: trace element contents of boninites and forearc basalts from IODP Expedition 352

NASA Astrophysics Data System (ADS)

Chapman, T.; Clarke, G. L.; Reagan, M. K.; Sakuyama, T.; Godard, M.; Shervais, J. W.; Prytulak, J.; Shimizu, K.; Nelson, W. R.; Heaton, D. E.; Whattam, S. A.; Li, H.; Pearce, J. A.

2016-12-01

The Izu-Bonin Mariana (IBM) forearc represents an ideal location to study the dynamics of subduction initiation and to reveal the volcanic sequences appropriate to assess ophiolite origins. The volcanic stratigraphy recovered on Expedition 352 illustrates an abrupt shift from forearc basalt (FAB) to boninite magmatism, with limited transitional rock types, as observed from submersible and previous drill work in the Izu-Bonin and Mariana sections. The transition represents a change from decompression melting to fluxed melting of the mantle wedge. The volcanic stratigraphy has several distinct boninite chemical evolution trends (basaltic boninite, low- and high-silica boninite). Mineral assemblages and phenocryst trace element compositions vary throughout the volcanic sequence providing an opportunity to explore more completely boninite and FAB transitions and petrogenesis. FABs are characterised by early plagioclase crystallization and HREE enriched clinopyroxene with high Ti contents. Basaltic boninite and some low-silica boninite lavas have overlapping REE concentrations consistent with early plagioclase growth preceded by clinopyroxene. In contrast, textures and HREE depleted concentrations of clinopyroxene in high-silica boninite imply late plagioclase growth relative to olivine and orthopyroxene. Variations in mineral compositions and paragenesis in boninites reflect changes in magma compositions and a progressive depletion of mantle sources over time. This is illustrated via key incompatible and compatible trace element ratios and concentrations (e.g. Zr/Ti & V or Cr). The transition from FAB to low-Si boninite was subtle in terms of mineral modes, but was more evident in terms of the phase and lava compositions.

Trace elemental correlation study in malignant and normal breast tissue by PIXE technique

NASA Astrophysics Data System (ADS)

Raju, G. J. Naga; Sarita, P.; Kumar, M. Ravi; Murty, G. A. V. Ramana; Reddy, B. Seetharami; Lakshminarayana, S.; Vijayan, V.; Lakshmi, P. V. B. Rama; Gavarasana, Satyanarayana; Reddy, S. Bhuloka

2006-06-01

Particle induced X-ray emission technique was used to study the variations in trace elemental concentrations between normal and malignant human breast tissue specimens and to understand the effects of altered homeostasis of these elements in the etiology of breast cancer. A 3 MeV proton beam was used to excite the biological samples of normal and malignant breast tissues. The elements Cl, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Rb and Sr were identified and their relative concentrations were estimated. Almost all the elements were found to be elevated (p < 0.05, Wilcoxon signed-ranks test) in the cancerous tissues when compared with normal tissues. The excess levels of trace elements observed in the cancerous breast tissues could either be a cause or a consequence of breast cancer. Regarding their role in the initiation or promotion of breast cancer, one possible interpretation is that the elevated levels of Cu, Fe and Cr could have led to the formation of free radicals or other reactive oxygen species (ROS) that adversely affect DNA thereby causing breast cancer, which is mainly attributed to genetic abnormalities. Moreover, since Cu and Fe are required for angiogenesis, elevated concentrations of these elements are likely to promote breast cancer by increasing the blood supply for tumor growth. On the other hand elevated concentrations of elements in breast cancer tissues might also be a consequence of the cancer. This can be understood in terms of the biochemical and histological differences between normal and cancerous breast tissues. Tumors, characterized by unregulated multiplication of cells, need an ever-increasing supply of essential nutrients including trace elements. This probably results in an increased vascularity of malignant tissues, which in turn leads to enhancement of elemental concentrations in tumors.

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.

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.

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).

The origin of low-K rhyolites from the mariana frontal arc

NASA Astrophysics Data System (ADS)

Meijer, A.

1983-08-01

Low-K rhyolites and overlying 2-pyroxene andesites, both of Late Eocene age, comprise the oldest volcanic units exposed on Saipan. The mineralogy and geologic setting of these rocks indicate they were erupted in a volcanic arc setting. The presence of andesite and lack of basalts of similar age suggest that the rhyolites are not part of a typical bimodal (basalt/rhyolite) suite. Major and trace element data indicate the Saipan andesites were not parental to the rhyolites. Out of various models evaluated for derivation of the rhyolites, the most reasonable involves crystal fractionation of a boninite series andesite that was very depleted in LIL elements. This andesite probably evolved from more mafic magmas which in turn were derived from the sub-arc mantle. Isotopic data suggest the mantle source for these magmas may have contained a minor seawater component.

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.

MORB mantle hosts the missing Eu (Sr, Nb, Ta and Ti) in the continental crust: New perspectives on crustal growth, crust-mantle differentiation and chemical structure of oceanic upper mantle

NASA Astrophysics Data System (ADS)

Niu, Yaoling; O'Hara, Michael J.

2009-09-01

We have examined the high quality data of 306 mid-ocean ridge basalt (MORB) glass samples from the East Pacific Rise (EPR), near-EPR seamounts, Pacific Antarctic Ridge (PAR), near-PAR seamounts, Mid-Atlantic Ridge (MAR), and near-MAR seamounts. The data show a correlated variation between Eu/Eu* and Sr/Sr*, and both decrease with decreasing MgO, pointing to the effect of plagioclase crystallization. The observation that samples with MgO > 9.5 wt.% (before plagioclase on the liquidus) show Eu/Eu* > 1 and Sr/Sr* > 1 and that none of the major phases (i.e., olivine, orthopyroxene, clinopyroxene, spinel and garnet) in the sub-ridge mantle melting region can effectively fractionate Eu and Sr from otherwise similarly incompatible elements indicates that the depleted MORB mantle (DMM) possesses excess Sr and Eu, i.e., [Sr/Sr*]DMM > 1 and [Eu/Eu*]DMM > 1. Furthermore, the well-established observation that DNb ≈ DTh, DTa ≈ DU and DTi ≈ DSm during MORB mantle melting, yet primitive MORB melts all have [Nb/Th]PMMORB > 1, [Ta/U]PMMORB > 1 and [Ti/Sm]PMMORB > 1 (where PM indicates primitive mantle normalized), also points to the presence of excess Nb, Ta and Ti in the DMM, i.e., [Nb/Th]PMDMM > 1, [Ta/U]PMDMM > 1 and [Ti/Sm]PMDMM > 1. The excesses of Eu, Sr, Nb, Ta and Ti in the DMM complement the well-known deficiencies of these elements in the bulk continental crust (BCC). These new observations, which support the notion that the DMM and BCC are complementary in terms of the overall abundances of incompatible elements, offer new insights into the crust-mantle differentiation. These observations are best explained by partial melting of amphibolite of MORB protolith during continental collision, which produces andesitic melts with a remarkable compositional (major and trace element abundances as well as key elemental ratios) similarity to the BCC, as revealed by andesites in southern Tibet produced during the India-Asia continental collision. An average amphibolite of MORB protolith consists of ~ 66.4% amphibole, ~ 29.2% plagioclase and 4.4% ilmenite. In terms of simple modal melting models, the bulk distribution coefficient ratios D2Eu/(Sm + Gd) = 1.21, D2Sr/(Pr + Nd) = 1.04, DNb/Th = 44, DTa/U = 57, DTi/Sm = 3.39 and DNb/Ta = 1.30 readily explains the small but significant negative Eu and Sr anomalies, moderate negative Ti anomaly and huge negative Nb and Ta anomalies as well as the more sub-chondritic Nb/Ta ratio in the syncollisional andesitic melt that is characteristic of and contributes to the continental crust mass. These results support the hypothesis that continental collision zones are primary sites of net continental crust growth, whereas the standard "island arc" model has many more difficulties than certainties. That is, it is the continental collision (vs. "island arc magmatism" or "episodic super mantle avalanche events") that produces and preserves the juvenile crust, and hence maintains net continental growth. The data also allow us to establish the robust composition of depleted and most primitive (or "primary") MORB melt with 13% MgO. This, together with the estimated positive Eu and Sr anomalies in the DMM, further permits estimation that the DMM may occupy the uppermost ~ 680 km of the convective mantle following the tradition that the DMM lies in the shallowest mantle. However, the tradition may be in error. The seismic low velocity zone (LVZ) may be compositionally stratified with small melt fractions concentrated towards the interface with the growing lithosphere because of buoyancy. Such small melt fractions, enriched in volatiles and incompatible elements, continue to metasomatize the growing lithosphere before it reaches the full thickness after ~ 70 Myrs. Hence, the oceanic mantle lithosphere is a huge enriched geochemical reservoir. On the other hand, deep portions of the LVZ, which are thus relatively depleted, become the primary source feeding the ridge because of ridge-suction-driven lateral material supply to form the crust and much of the lithosphere at and in the vicinity of the ridge.

Preliminary study on multi-element profile mapping of crustal and mantle zircons by using Synchrotron Radiation X-ray Fluorescence (SR-XRF)

NASA Astrophysics Data System (ADS)

Hasözbek, Altug; Shyam, Badri; Siebel, Wolfgang; Schmitt, Axel; Akay, Erhan; Skinner, Lawrie

2013-04-01

Zircon (ZrSiO4) is a mineral of singular importance in the geosciences. Zircon microanalysis has greatly contributed to our understanding of key events in earth's history as certain radioactive heavy elements and their daughter products are well-preserved within the exceptionally stable inorganic matrix of the mineral. A prevailing notion in this field is that zircon, as a mineral, is predominantly a crustal mineral; this has been contested in the last few years with more reports of mantle-derived zircons (Siebel et al., 2009). Zircons enriched from different parts of the upper mantle to lower crust from Turkey (Hasozbek et al. 2010) and Germany (Siebel et al., 2009) will be presented in this study using SR-XRF mapping carried out at beamline 2-IDE at the Advanced Photon Source synchrotron facility (Argonne National Laboratory, USA). The high-resolution (5-10 µm) elemental maps were obtained with collimated and linearly polarized synchrotron radiation (10 to 17 keV) and possess the advantage of being a completely non-destructive technique. Elemental maps of various trace and rare-earth elements along the cross-section of the zircons reveal a zonation-related distribution, which may be used to reveal factors affecting the growth history and dynamics of the crystal formation. Further, abrupt changes in elemental distribution or concentration were found to correspond to faults or inclusions within the zircon crystal. If such observations are found to be applicable for a wide range of samples, elemental mapping with this technique may serve as an important qualitative diagnostic to locating µ-meter inclusions that may be challenging to identify using other techniques (ICP-MS LA, SHRIMP,…) Through these preliminary elemental profile mapping studies of crustal and mantle zircons using SR-XRF methods, we aim to highlight a relatively quick and promising analytical method that may be used to study various geological problems.

Isotopic and trace element compositions of upper mantle and lower crustal xenoliths, Cima volcanic field, California: Implications for evolution of the subcontinental lithospheric mantle

USGS Publications Warehouse

Mukasa, S.B.; Wilshire, H.G.

1997-01-01

Ultramafic and mafic xenoliths from the Cima volcanic field, southern California, provide evidence of episodic modification of the upper mantle and underplating of the crust beneath a portion of the southern Basin and Range province. The upper mantle xenoliths include spinel peridotite and anhydrous and hydrous pyroxenite, some cut by igneous-textured pyroxenite-gabbro veins and dikes and some by veins of amphibole ?? plagioclase. Igneous-textured pyroxenites and gabbros like the dike rocks also occur abundantly as isolated xenoliths inferred to represent underplated crust. Mineral and whole rock trace element compositions among and within the different groups of xenoliths are highly variable, reflecting multiple processes that include magma-mantle wall rock reactions, episodic intrusion and it filtration of basaltic melts of varied sources into the mantle wall rock, and fractionation. Nd, Sr, and Pb isotopic compositions mostly of clinopyroxene and plagioclase mineral separates show distinct differences between mantle xenoliths (??Nd = -5.7 to +3.4; 87Sr/86Sr = 0.7051 - 0.7073; 206Pb/204Pb = 19.045 - 19.195) and the igneous-textured xenoliths (??Nd = +7.7 to +11.7; 87Sr/86Sr = 0.7027 - 0.7036 with one carbonate-affected outlier at 0.7054; and 206Pb/204Pb = 18.751 - 19.068), so that they cannot be related. The igneous-textured pyroxenites and gabbros are similar in their isotopic compositions to the host basaltic rocks, which have ??Nd of+5.1 to +9.3; 87Sr/86Sr of 0.7028 - 0.7050, and 206Pb/204Pb of 18.685 - 21.050. The igneous-textured pyroxenites and gabbros are therefore inferred to be related to the host rocks as earlier cogenetic intrusions in the mantle and in the lower crust. Two samples of peridotite, one modally metasomatized by amphibole and the other by plagioclase, have isotopic compositions intermediate between the igneous-textured xenoliths and the mantle rock, suggesting mixing, but also derivation of the metasomatizing magmas from two separate and distinct sources. Sm-Nd two-mineral "isochrons" yield apparent ages for petrographically identical rocks believed to be coeval ranging from -0 to 113 ?? 26 Ma, indicating the unreliability of dating these rocks with this method. Amphibole and plagioclase megacrysts are isotopically like the host basalts and probably originate by mechanical breakup of veins comagmatic with the host basaltic rocks. Unlike other Basin and Range localities, Cima Cr-diopside group isotopic compositions do not overlap with those of the host basalts. Copyright 1997 by the American Geophysical Union.

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.

Along and Across Arc Variation of the Central Andes by Single Crystal Trace Element Analaysis

NASA Astrophysics Data System (ADS)

Michelfelder, G.; Sundell, T.; Wilder, A.; Salings, E. E.

2017-12-01

Along arc and across arc geochemical variations at continental volcanic arcs are influenced by a number of factors including the composition and thickness of the continental crust, mantle heterogeneity, and fluids from the subducted slab. Whole rock geochemical trends along and across the arc front of the Central Volcanic Zone (CVZ) have been suggested to be primarily influenced by the composition and thickness of the crust. In the CVZ, Pb isotopic domains relate volcanic rock compositions to the crustal basement and systematically varies with crustal age. It has been shown repeatedly that incompatible trace element trends and trace element ratios can be used to infer systematic geochemical changes. However, there is no rule linking magmatic process or chemical heterogeneity/ homogeneity as a result of large crustal magma storage reservoirs such as MASH zones to the observed variation. Here we present a combination of whole rock major- and trace element data, isotopic data and in situ single crystal data from plagioclase, pyroxene and olivine for six stratovolcanoes along the arc front and in the back arc of the CVZ. We compare geochemical trends at the whole and single crystal scale. These volcanoes include lava flows and domes from Cerro Uturuncu in the back-arc, Aucanquilcha, Ollagüe, San Pedro-San Pablo, Lascar, and Lazufre from the arc front. On an arc-wide scale, whole rock samples of silicic lavas from these six composite volcanoes display systematically higher K2O, LILE, REE and HFSE contents and 87Sr/86Sr ratios with increasing distance from the arc-front. In contrast, the lavas have systematically lower Na2O, Sr, and Ba contents; LILE/HFSE ratios; 143Nd/144Nd ratios; and more negative Eu anomalies. Silicic magmas along the arc-front reflecting melting of young, mafic composition source rocks with the continental crust becoming increasingly older and more felsic toward the east. These trends are paralleled in the trace element compositions of plagioclase cores which systematically become less diverse in composition in younger lava flows from each center. We suggest these trends result from progressively smaller degrees of mantle partial melting, primary melt generation, and crustal hybridization with distance from the arc-front and varying influence of MASH zone processes.

[Discussion on diagenesis of Xilingang pluton-constrained by X-ray Fluorescence spectroscopy, plasma mass spectrometry and Raman spectroscopy].

PubMed

Tang, Yu-Kun; Chen, Guo-Neng; Zhang, Ke; Huang, Hai-Hua

2013-05-01

The results on Xilingang pluton, mainly consisting of red beds, granites containing numerous debris of red beds and granites, obtained by X-ray fluorescence spectroscopy, plasma mass spectrometry and Raman spectroscopy show: (1) Xilingang pluton from red beds, granites containing numerous debris of red beds to granites has obvious characteristics of decreasing silicon and alkali content, and rising ignition loss, dark mineral content and oxidation index; (2) Chondrite-normalized REE distribution curves and primitive mantle-normalized spider diagram for trace elements of redbed, granites containing numerous debris of red beds and granites have a good consistency, the distribution characteristics of elements are similar to Nanling transformation-type granite; (3) The value of Raman spectrogram characteristic peak of quartz crystal in Xilingang granite decreased from the center of quartz crystal, and FWHM is steady. According to the above, the authors believe that Xilingang granite formed was related to in-situ melting of red beds and underlying strata and magma consolidation. Volatile components were discharged continuously, and oxidation index decreased gradually in the melting process. In the process of diagenesis, the top of pluton tend to be an ongoing silicon and alkali increase, while TFeO and MgO continue to migrate to bottom, and crystallization environment is a relatively closed and steady system.

Length-scales of chemical and isotopic heterogeneity in the mantle section of the Shetland Ophiolite Complex, Scotland

NASA Astrophysics Data System (ADS)

O'Driscoll, B.; Walker, R. J.; Clay, P. L.; Day, J. M. D.; Ash, R. D.; Daly, J. S.

2018-04-01

Kilometre to sub-metre scale heterogeneities have been inferred in the oceanic mantle based on sampling of both ophiolites and abyssal peridotites. The ∼492 Ma Shetland Ophiolite Complex (SOC) contains a well-preserved mantle section that is dominated by harzburgite (∼70 vol.%) previously reported to have variable major and trace element compositions, yet dominantly chondritic initial 187Os/188Os compositions. To assess the preservation of compositional heterogeneities at sub-metre length-scales in the oceanic mantle, a ∼45 m2 area of the SOC mantle section was mapped and sampled in detail. Harzburgites, dunites and a pyroxenite from this area were analysed for lithophile and highly-siderophile element (HSE) abundances, as well as for 187Os/188Os ratios. Lithophile element data for most rocks are characteristic of supra-subduction zone (SSZ) metasomatic processes. Two dunites have moderately fractionated HSE patterns and suprachondritic γOs(492 Ma) values (+5.1 and +7.5) that are also typical of ophiolitic dunites generated by SSZ melt-rock interactions. By contrast, six harzburgites and four dunites have approximately chondritic-relative abundances of Os, Ir and Ru, and γOs(492 Ma) values ranging only from -0.6 to +2.7; characteristics that imply no significant influence during SSZ processes. Two harzburgites are also characterised by significantly less radiogenic γOs(492 Ma) values (-3.5 and -4), and yield Mesoproterozoic time of Re depletion (TRD) model ages. The range of Os isotope compositions in the studied area is comparable to the range reported for a suite of samples representative of the entire SOC mantle section, and approaches the total isotopic variation of the oceanic mantle, as observed in abyssal peridotites. Mechanisms by which this heterogeneity can be formed and preserved involve inefficient and temporally distinct melt extraction events and strong localised channelling of these melts.

Partition Coefficients at High Pressure and Temperature

NASA Astrophysics Data System (ADS)

Righter, K.; Drake, M. J.

2003-12-01

Differentiation of terrestrial planets includes separation of a metallic core and possible later fractionation of mineral phases within either a solid or molten mantle (Figure 1). Lithophile and siderophile elements can be used to understand these two different physical processes, and ascertain whether they operated in the early Earth. The distribution of elements in planets can be understood by measuring the partition coefficient, D (ratio of concentrations of an element in different phases (minerals, metals, or melts)). (14K)Figure 1. Schematic cross-section through the Earth, showing: (a) an early magma ocean stage and (b) a later cool and differentiated stage. The siderophile elements (iron-loving) encompass over 30 elements and are defined as those elements for which D(metal/silicate)>1, and are useful for deciphering the details of core formation. This group of elements is commonly broken up into several subclasses, including the slightly siderophile elements (1104). Because these three groups encompass a wide range of partition coefficient values, they can be very useful in trying to determine the conditions under which metal may have equilibrated with the mantle (or a magma ocean). Because metal and silicate may equilibrate by several different mechanisms, such as at the base of a deep magma ocean, or as metal droplets descend through a molten mantle, partition coefficients can potentially shed light on which mechanism may be most important, thus linking the physics and chemistry of core formation. In this chapter, we summarize metal/silicate partitioning of siderophile elements and show how they may be used to understand planetary core formation.Once a planet is differentiated into core and mantle, a mantle will cool during convection, and can start in either a molten or solid state, depending upon the initial thermal conditions. If hot enough, minerals will crystallize from a molten mantle, and become entrained in the convecting melt, or eventually settle out at the bottom. The entrainment and settling process has been studied in detail (e.g., Tonks and Melosh, 1990), and is a potential mechanism for differentiation between the deep and shallow parts of Earth's mantle. The lithophile elements, those elements that have D(metal/silicate) <1, fall into many different subclasses and all hold information about the deep mineral structure of the mantle. Rare-earth elements (REEs) have proven to be useful: europium anomalies have helped elucidate the role of plagioclase in lunar crust formation (e.g., Schnetzler and Philpotts, 1971; Weill et al., 1974), and LREE/HREE depletion and enrichment are indicators of partial melting in the presence of garnet in the mantle. High-field-strength elements (HFSEs) - niobium, zirconium, tantalum, and hafnium - are all refractory and hence more resilient to fractionation processes such as volatility or condensation. They also have an affinity for ilmenite and rutile, and can explain differences between lunar and martian samples as well as features of Earth's continental crust ( Taylor and McLennan, 1985). Alkaline-earth and alkaline elements include rubidium, strontium, barium, potassium, caesium, and calcium, some of which are involved in radioactive decay couples, e.g., Rb-Sr and K-Ar. The latter is important in understanding the contribution of radioactive decay to planetary heat production, and potential deep sources of radiogenic argon (see Chapter 2.06). Rubidium and potassium are further useful as tracers of hydrous phases such as mica and amphibole. Possible fractionation of any of these elements from chondritic abundances (see Chapter 2.01) can be assessed with the knowledge of partition coefficients. In this chapter we summarize our understanding of mineral/melt fractionation of minor and trace elements at high pressures and temperatures and discuss the implications for mantle differentiation.

Geochemistry of Groundwater

NASA Astrophysics Data System (ADS)

Chapelle, F. H.

2003-12-01

Differentiation of terrestrial planets includes separation of a metallic core and possible later fractionation of mineral phases within either a solid or molten mantle (Figure 1). Lithophile and siderophile elements can be used to understand these two different physical processes, and ascertain whether they operated in the early Earth. The distribution of elements in planets can be understood by measuring the partition coefficient, D (ratio of concentrations of an element in different phases (minerals, metals, or melts)). (14K)Figure 1. Schematic cross-section through the Earth, showing: (a) an early magma ocean stage and (b) a later cool and differentiated stage. The siderophile elements (iron-loving) encompass over 30 elements and are defined as those elements for which D(metal/silicate)>1, and are useful for deciphering the details of core formation. This group of elements is commonly broken up into several subclasses, including the slightly siderophile elements (1104). Because these three groups encompass a wide range of partition coefficient values, they can be very useful in trying to determine the conditions under which metal may have equilibrated with the mantle (or a magma ocean). Because metal and silicate may equilibrate by several different mechanisms, such as at the base of a deep magma ocean, or as metal droplets descend through a molten mantle, partition coefficients can potentially shed light on which mechanism may be most important, thus linking the physics and chemistry of core formation. In this chapter, we summarize metal/silicate partitioning of siderophile elements and show how they may be used to understand planetary core formation.Once a planet is differentiated into core and mantle, a mantle will cool during convection, and can start in either a molten or solid state, depending upon the initial thermal conditions. If hot enough, minerals will crystallize from a molten mantle, and become entrained in the convecting melt, or eventually settle out at the bottom. The entrainment and settling process has been studied in detail (e.g., Tonks and Melosh, 1990), and is a potential mechanism for differentiation between the deep and shallow parts of Earth's mantle. The lithophile elements, those elements that have D(metal/silicate) <1, fall into many different subclasses and all hold information about the deep mineral structure of the mantle. Rare-earth elements (REEs) have proven to be useful: europium anomalies have helped elucidate the role of plagioclase in lunar crust formation (e.g., Schnetzler and Philpotts, 1971; Weill et al., 1974), and LREE/HREE depletion and enrichment are indicators of partial melting in the presence of garnet in the mantle. High-field-strength elements (HFSEs) - niobium, zirconium, tantalum, and hafnium - are all refractory and hence more resilient to fractionation processes such as volatility or condensation. They also have an affinity for ilmenite and rutile, and can explain differences between lunar and martian samples as well as features of Earth's continental crust ( Taylor and McLennan, 1985). Alkaline-earth and alkaline elements include rubidium, strontium, barium, potassium, caesium, and calcium, some of which are involved in radioactive decay couples, e.g., Rb-Sr and K-Ar. The latter is important in understanding the contribution of radioactive decay to planetary heat production, and potential deep sources of radiogenic argon (see Chapter 2.06). Rubidium and potassium are further useful as tracers of hydrous phases such as mica and amphibole. Possible fractionation of any of these elements from chondritic abundances (see Chapter 2.01) can be assessed with the knowledge of partition coefficients. In this chapter we summarize our understanding of mineral/melt fractionation of minor and trace elements at high pressures and temperatures and discuss the implications for mantle differentiation.

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.

Progress of pharmacogenomic research related to minerals and trace elements.

PubMed

Zeng, Mei-Zi; Tang, Jie; Liu, Zhao-Qian; Zhou, Hong-Hao; Zhang, Wei

2015-10-01

Pharmacogenomics explores the variations in both the benefits and the adverse effects of a drug among patients in a target population by analyzing genomic profiles of individual patients. Minerals and trace elements, which can be found in human tissues and maintain normal physiological functions, are also in the focus of pharmacogenomic research. Single-nucleotide polymorphisms (SNPs) affect the metabolism, disposition and efficacy of minerals and trace elements in humans, resulting in changes of body function. This review describes some of the recent progress in pharmacogenomic research related to minerals and trace elements.

Tracking the depleted mantle signature in melt inclusions and host glass of basaltic martian shergottites using secondary ionization mass spectrometry

NASA Astrophysics Data System (ADS)

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

2013-12-01

Trace element abundances of depleted shergottite magmas recorded by olivine-hosted melt inclusions (MI) and interstitial mesostasis glass were measured using the CAMECA ims-1270 ion microprobe. Two meteorites: Tissint, an olivine-phyric basaltic shergottite which fell over Morocco July 18th 2001; and the Antarctic meteorite Yamato 980459 (Y98), an olivine-phyric basaltic shergottite with abundant glassy mesostasis have been studied. Chondrite-normalized REE patterns for MI in Tissint and Y98 are characteristically LREE depleted and, within analytical uncertainty, parallel those of their respective whole rock composition; supporting each meteorite to represent a melt composition that has experienced closed-system crystallization. REE profiles for mesostasis glass in Y98 lie about an order of magnitude higher than those from the MI; with REE profiles for Tissint MI falling in between. Y98 MI have the highest average Sm/Nd and Y/Ce ratios, reflecting their LREE depletion and further supporting Y98 as one of our best samples to probe the depleted shergotitte mantle. In general, Zr/Nb ratios overlap between Y98 and Tissint MI, Ce/Nb ratios overlap between Y98 MI and mesostasis glass, and Sm/Nd ratios overlap between Y98 mesostasis glass and Tissint MI. These features support similar sources for both, but with subtle geochemical differences that may reflect different melting conditions or fractionation paths during ascent from the mantle. Interestingly, the REE patterns for all analyses in Y98 and possibly for those from Tissint as well display a flattening of the LREE that suggests an early crustal contribution to the shergottite mantle.

Nuclear microscopy in trace-element biology — from cellular studies to the clinic

NASA Astrophysics Data System (ADS)

Lindh, Ulf

1993-05-01

The concentration and distribution of trace and major elements in cells are of great interest in cell biology. PIXE can provide elemental concentrations in the bulk of cells or organelles as other bulk techniques such as atomic absorption spectrophotometry and nuclear activation analysis. Supplementary information, perhaps more exciting, on the intracellular distributions of trace elements can be provided using nuclear microscopy. Intracellular distributions of trace elements in normal and malignant cells are presented. The toxicity of mercury and cadmium can be prevented by supplementation of the essential trace element selenium. Some results from an experimental animal model are discussed. The intercellular distribution of major and trace elements in isolated blood cells, as revealed by nuclear microscopy, provides useful clinical information. Examples are given concerning inflammatory connective-tissue diseases and the chronic fatigue syndrome.

Continental crustal formation and recycling: Evidence from oceanic basalts

NASA Technical Reports Server (NTRS)

Saunders, A. D.; Tarney, J.; Norry, M. J.

1988-01-01

Despite the wealth of geochemical data for subduction-related magma types, and the clear importance of such magmas in the creation of continental crust, there is still no concensus about the relative magnitudes of crustal creation versus crustal destruction (i.e., recycling of crust into the mantle). The role of subducted sediment in the formation of the arc magmas is now well documented; but what proportion of sediment is taken into the deeper mantle? Integrated isotopic and trace element studies of magmas erupted far from presently active subduction zones, in particular basaltic rocks erupted in the ocean basins, are providing important information about the role of crustal recycling. By identifying potential chemical tracers, it is impossible to monitor the effects of crustal recycling, and produce models predicting the mass of material recycled into the mantle throughout long periods of geological time.

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.

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.

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.

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.

Petrogenesis of Pliocene Alkaline Volcanic Rocks from Southeastern Styrian Basin, Austria

NASA Astrophysics Data System (ADS)

Ali, Sh.; Ntaflos, Th.

2009-04-01

Petrogenesis of Pliocene Alkaline Volcanic Rocks from Southeastern Styrian Basin, Austria Sh. Ali and Th. Ntaflos Dept. of Lithospheric Research, University of Vienna, Austria Neogene volcanism in the Alpine Pannonian Transition Zone occurred in a complex geodynamic setting. It can be subdivided into a syn-extentional phase that comprises Middle Miocene dominantly potassic, intermediate to acidic volcanism and a post-extensional phase, which is characterized by eruption of alkaline basaltic magmas during the Pliocene to Quartenary in the Styrian Basin. These alkaline basaltic magmas occur as small eruptive centers dominating the geomorphology of the southeastern part of the Styrian Basin. The eruptive centers along the SE Styrian Basin from North to South are: Oberpullendorf, Pauliberg, Steinberg, Strandenerkogel, Waltrafelsen and Klöch. The suite collected volcanic rocks comprise alkali basalts, basanites and nephelinites. Pauliberg: consists of alkali basalts that exhibit a narrow range of SiO2 (44.66-47.70 wt %) and wide range of MgO (8.52-13.19-wt %), are enriched in TiO2 (3.74-4.18 wt %). They are enriched in incompatible trace elements such as Zr (317-483 ppm), Nb (72.4-138 ppm) and Y (30.7-42 ppm). They have Nb/La ratio of 1.89 (average) and Cen/Ybn=15.22-23.11. Oberpullendorf: it also consists of alkali basalts with higher SiO2 (50.39 wt %) and lower TiO2 (2.80 wt %) if compared with the Pauliberg suite. Incompatible trace elements are lower than in Pauliberg; Zr =217 ppm, Nb=49.8 ppm, Y=23.6 ppm and Nb/La=1.93. The Oberpullendorf alkalibasalts are relative to Pauliberg lavas more depleted in LREE (Cen/Ybn=12.78). Steinberg: it consists of basanites with SiO2=44.49-46.85 wt %, MgO=6.30-9.13-wt %, and TiO2 =2.09-2.26 wt %. They are enriched in incompatible trace elements such as Zr (250-333 ppm), Nb (94-130 ppm), Y (24.7-31.9 ppm) and Nb/La=1.59 (average). The Cen/Ybn ratio varies between 18.17 and 22.83 indicating relative steep REE chondrite normalized patterns. Strandenerkogel: it consists of nephelinites with narrow compositional ranges; SiO2 =40.99-42.44 wt %, MgO=6.63-6.92 wt % and TiO2=2.03-2.07 wt %. They are enriched in incompatible trace elements such as Zr (362-382 ppm), Nb (139-153 ppm) and Y (39.5-40.7 ppm). They have Nb/La ratio of 1.20 and are strongly enriched in LREE (Cen/Ybn=25.04-28.11). Waltrafelsen: there are like in Strandenerkogel and have SiO2=42.42 wt %, MgO=6.55 wt %, and TiO2=2.01 wt %. The incompatible trace elements such as Zr (362 ppm), Nb (145 ppm) and Y (38.3 ppm) are similar to that of Stranerkogel. They have Nb/La ratio of 1.27 and are strongly enriched in LREE (Cen/Ybn=24.92). Klöch: it consists of basanites with similar to Steinberg composition (SiO2=45.34-46.60 wt %, MgO=8.98-10.11 wt %, and TiO2= 2.28-2.37 wt %. Incompatible trace elements such as Zr (252-273 ppm), Nb (94.2-101 ppm) and Y (24.4-27.2 ppm) are high. They have Nb/La ratio of 1.71 (average). Their REE abundances compared to Steinberg are slightly lower (Cen/Ybn=18.19-20.17). The Nb/La ratio of all the studied rock varieties is greater than one indicates an OIB-like asthenospheric mantle source for the basaltic magma. All the studied rock varieties except alkali basalts of Pauliberg have Tbn/Ybn ratios which are comparable to those of the alkali basalts of Hawaii ((Tbn/Ybn range from 1.89 to 2.45); the Hawaiian basalts are considered to have been derived from a garnet-lherzolite mantle source (Frey et al. 1991; McKenzie & O'Nions, 1991). The chondrite normalized HREE abundances indicate the presence of garnet as a residual phase in the melt source region as can be inferred from the Dy/Yb ratio (average 2.93) which is greater than that of chondritic Dy/Yb ratio (1.57) All the studied rock varieties display alkaline affinity and negative K-anomaly. The negative K-anomaly suggests either a source character, (e.g. frozen HIMU-like veins or pockets in the depleted lherzolite)? or it is consistent with the presence of a K-bearing hydrous phase in the residual mantle. References FREY, F. A., GARCIA, M. O., WISE, W. S., KENNEDY, A., GURRIET, P. & ALBAREDE, F. 1991. The evolution of Mauna Kea volcano, Hawaii: Petrogenesis of tholeiitic and alkali basalts. Journal of Geophysical Research 96, 14347-75. MCKENZIE, D. P. & O'NIONS, R. K. 1991. Partial melting distributions from inversion of rare earth element concentrations. Journal of Petrology 32, 1021-91.

Primitive Melt Inclusions from Multiple Samples from the FAMOUS Zone: Insights into the Mantle Melting Column and the Fractionation Processes

NASA Astrophysics Data System (ADS)

Laubier, M.; Langmuir, C. H.

2008-12-01

On mid-ocean ridges, the influential work by Sobolev and Shimizu (Nature, 1993) and Sobolev (Petrology, 1996) has inferred fractional melting during polybaric upwelling by showing that olivine-hosted inclusions were formed over a range of pressures. However melt inclusion studies have often concerned single MORB samples and may be seen as anecdotal in the sense that they are neither repeated nor globally verified. Recent modeling and experimental results also suggest the importance of post-entrapment processes for major and trace elements. This study presents major and trace element data in 300 olivine-hosted melt inclusions from 11 samples from the FAMOUS segment on the Mid-Atlantic Ridge. Published data from Shimizu (Phys. Earth Planet. Int., 1998) and Kamenetsky (EPSL, 1996; spinel-hosted inclusions) are also reported. In parallel, major and trace element measurements were performed in 150 glasses of the segment in order to have consistent datasets. Melt inclusions, trapped in olivine phenocrysts Mg#85-92, display complex trends in major element plots and can be divided into three groups. Group 1, the largest, is characterized by high MgO (9.4-13.4 wt.%), intermediate SiO2 and Al2O3 contents. Group 2 displays distinctively high Al2O3 (up to 18.4 wt.%), low SiO2 (as low as 46.5 wt.%) and high MgO (10.5-12.8 wt.%) contents, along with low CaO and variable TiO2, K2O and incompatible element concentrations. Group 3 consists of the melt inclusions trapped in less primitive olivines (Mg#<88.5) and displays higher SiO2, CaO and trace element contents. In the lava population, two groups can be distinguished. A small subset, that shares many features with the group 2 melt inclusions, displays high MgO and Al2O3 and low SiO2 and incompatible element contents. This type of lava - high-Al, low-Si and high-Mg - has been previously reported for various mid-ocean ridges (e.g., le Roux et al., Contrib. Min. Petrol., 2002; Eason and Sinton, EPSL, 2008). The second group plots along liquid lines of descent at low pressure starting from the compositions of the group 1 melt inclusions. Modeling of continuous polybaric melting and crystallization shows that the different inclusion groups are derived from melts formed at various pressures in the melting column (~12-6 kbar). After segregation from the mantle, the three batches of melts are fractionated at distinct pressures. The group 2 melt inclusions are consistent with the highest pressure of melt formation and a major role of cpx+olivine fractionation at high pressure (8 kbar), whereas group 3 results indicate the lowest pressure of extraction and entrapment (1kbar). An important observation is that high-Al, low-Si lavas contain melt inclusions from both the low-Si, high-Al group 2 and normal compositions (groups 1 and 3). These lavas can be reproduced by mixing between these two populations of inclusions, followed by some extent of differentiation. Therefore, this study shows that lavas represent averages of melts differentiated from the melt inclusions, and that the major element variability among inclusions can be explained by the combined effects of polybaric melting and crystallization at variable pressure. Trace element compositions of group 1 and 2 melt inclusions show large variations; incompatible element ratios (Ba/La, Rb/Nb, etc) suggest local source heterogeneity. Further modeling will be carried out in order to distinguish between the effects of partial melting and source composition.

Boninite-like intraplate magmas from Manihiki Plateau require ultra-depleted and enriched source components

PubMed Central

Golowin, Roman; Portnyagin, Maxim; Hoernle, Kaj; Hauff, Folkmar; Gurenko, Andrey; Garbe-Schönberg, Dieter; Werner, Reinhard; Turner, Simon

2017-01-01

The Ontong Java and Manihiki oceanic plateaus are believed to have formed through high-degree melting of a mantle plume head. Boninite-like, low-Ti basement rocks at Manihiki, however, imply a more complex magma genesis compared with Ontong Java basement lavas that can be generated by ∼30% melting of a primitive mantle source. Here we show that the trace element and isotope compositions of low-Ti Manihiki rocks can best be explained by re-melting of an ultra-depleted source (possibly a common mantle component in the Ontong Java and Manihiki plume sources) re-enriched by ≤1% of an ocean-island-basalt-like melt component. Unlike boninites formed via hydrous flux melting of refractory mantle at subduction zones, these boninite-like intraplate rocks formed through adiabatic decompression melting of refractory plume material that has been metasomatized by ocean-island-basalt-like melts. Our results suggest that caution is required before assuming all Archaean boninites were formed in association with subduction processes. PMID:28181497

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.

Noble Gases Trace Earth's Subducted Water Flux

NASA Astrophysics Data System (ADS)

Smye, A.; Jackson, C.; Konrad-Schmolke, M.; Parman, S. W.; Ballentine, C. J.

2016-12-01

Volatile elements are transported from Earth's surface reservoirs back into the mantle during subduction of oceanic lithosphere [e.g. 1]. Here, we investigate the degree to which the fate of slab-bound noble gases and water are linked through the subduction process. Both water and noble gases are soluble in ring-structured minerals, such as amphibole, that are common constituents of subducted oceanic lithosphere. Heating and burial during subduction liberates noble gases and water from minerals through a combination of diffusion and dissolution. Combining a kinetic model, parameterized for noble gas fractionation in amphibole [2], with thermodynamic phase equilibria calculations, we quantify the effect of subduction dehydration on the elemental composition of slab-bound noble gases. Results show that post-arc slab water and noble gas fluxes are highly correlated. Hot subduction zones, which likely dominate over geologic history, efficiently remove noble gases and water from the down-going slab; furthermore, kinetic fractionation of noble gases is predicted to occur beneath the forearc. Conversely, hydrated portions of slab mantle in cold subduction zones transport noble gases and water to depths exceeding 200 km. Preservation of seawater-like abundances of Ar, Kr and Xe in the convecting mantle [1] implies that recycling of noble gases and water occurred during cold subduction and that the subduction efficiency of these volatile elements has increased over geological time, driven by secular cooling of the mantle. [1] Holland, G. and Ballentine, C. (2006). Nature 441, 186-191. [2] Jackson et al. (2013). Nat.Geosci. 6, 562-565.

Geochemical Evolution of the Louisville Seamount Chain

NASA Astrophysics Data System (ADS)

Vanderkluysen, L.; Mahoney, J. J.; Koppers, A. A.; Lonsdale, P. F.

2007-12-01

The Louisville seamount chain is a 4300 km long chain of submarine volcanoes in the southwestern Pacific that is commonly thought to represent a hotspot track. It spans an ~80 Myr age range, comparable to that of the Hawaiian-Emperor chain (Koppers et al., G-cubed, 5 (6), 2004). The few previously dredged igneous samples are dominantly basaltic and alkalic, and have been inferred to represent post-shield volcanism (Hawkins et al., AGU Monograph, 43, 235, 1987). Their isotope and trace element signatures suggest an unusually homogenous mantle source (Cheng et al., AGU Monograph, 43, 283, 1987). Dredging in 2006, during the AMAT02RR cruise of the R.V. Revelle, was carried out in the hope of recovering both shield and post-shield samples and of exploring the geochemical evolution of the chain. Igneous rocks were recovered from 33 stations on 23 seamounts covering some 47 Myr of the chain's history. Our study, focusing on the major and trace element and Sr, Nd and Pb isotopic characteristics of these samples, shows that all are alkalic basalts, basanites and tephrites containing normative nepheline. Variations in major and trace elements appear to be controlled predominantly by variable extents of melting and fractional crystallization, with little influence from mantle source heterogeneity. Indeed, age-corrected isotopic values define only a narrow range, in agreement with long-term source homogeneity relative to the scale of melting; e.g., ɛNd varies from +4.1 to +5.7, 206Pb/204Pb from 19.048 to 19.281, and 87Sr/86Sr from 0.70362 to 0.70398. These values broadly fall within the fields of the proposed "C" or "FOZO" mantle end-members. However, small variations are present, with less radiogenic Nd and Pb isotope ratios at the older, western end of the chain, defining a trend toward a broadly EM2-like composition. Although some workers have postulated that the Louisville hotspot was the source of the ~120 Myr Ontong Java Plateau, our samples are isotopically distinct from any known Ontong Java compositions.

Geochemical associations between fluorite mineralization and A-type shoshonitic magmatism in the Keban-Elazig area, East Anatolia, Turkey

NASA Astrophysics Data System (ADS)

Akgul, Bunyamin

2015-11-01

Keban fluorite mineralizations are closely related Coniacian-Campanian subvolcanics intruded into Permian-Triassic Keban metamorphites; this event caused pyrometasomatic, porphyry, and vein-type Pb-Zn-Ag, Cu, W, and Pb-Zn-Ag-Mo-F mineralizations. These rocks are syenitic and syenomonzonitic in composition and have high Al2O3, alkali (Na2O + K2O), FeO*/MgO, Zr, Nb, Ta, Ga, Rb, Y, and rare earth element (REE) contents. They are A-type, metaluminous, and all fall in the shoshonitic series field in K2O vs SiO2 and Th/Yb vs Ta/Yb diagrams. The trace element contents and discriminations indicate that the Keban syenitoids were derived from lithospheric mantle metasomatized by oceanic-crust/sediment fluids. The metal and halogen contents of the Keban mineralizations apparently originated from metasomatized mantle and were transported to the crust by syenitoid magmas. Clear resemblances in chondrite-normalized REE patterns, LREE-HREE partionation, and high LILE contents of the magmatics and fluorites indicate a close kinship between the syenitoids and fluorite mineralizations. The HFSE contents of the fluorites are lower than those of the magmatics, as HFSEs are not soluble in aqueous fluids. The fluorites are products of early-phase alkali magmatism (LREE > HREE). The high contents of Rb, Sr, and Ba of fluorites are inherited from the magma, which also has very high contents of these elements. In Sc-∑REE, (La/Yb)n-(Eu/Eu*)n and (Tb/La)n-(Tb/Ca)n diagrams, Keban fluorites fall into distinct areas from Akcakisla-Akdagmadeni and Celikhan-Adiyaman fluorites.

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.

Influence of sediment recycling on the trace element composition of primitive arc lavas

NASA Astrophysics Data System (ADS)

Collinet, M.; Jagoutz, O. E.

2017-12-01

Primitive calc-alkaline lavas from continental arcs are, on average, enriched in incompatible elements compared to those from intra-oceanic arcs. This relative enrichment is observed in different groups of trace elements: LILE (e.g. K, Rb), LREE to MREE (La-Dy) and HFSE (e.g.Zr, Nb) and is thought to result from (1) a transfer of material from the subducting slab to the mantle wedge at higher temperature than in intra-oceanic margins and/or (2) lower average degrees of melting in the mantle wedge, as a consequence of thicker overlying crusts and higher average pressures of melting. In addition to thicker overlying crusts and generally higher slab temperatures, continental margins are characterized by larger volumes of rock exposed above sea level and enhanced erosion rates compared to intra-oceanic arcs. As several geochemical signatures of arc lavas attest to the importance of sediment recycling in subduction zones, we explore the possibility that the high concentrations of incompatible elements in primitive lavas from continental arcs directly reflect a larger input of sediment to the subduction system. Previous efforts to quantify the sediment flux to oceanic trenches focused on the thickness of pelagic and hemipelagic sediments on top of the plate entering the subduction zone (Plank and Langmuir, 1993, Nature). These estimates primarily relied on the sediment layer drilled outboard from the subduction system and likely underestimate the volume of sediment derived from the arc itself. Accordingly, we find that such estimates of sediment flux do not correlate with the concentration of incompatible elements in primitive arc lavas. To account for regional contributions of coarser detrital sediments, usually delivered to oceanic trenches by turbidity currents, we apply to arc segments a model that quantifies the sediment load of rivers based on the average relief, area, temperature and runoff of their respective drainage areas (Syvitski et al., 2003, Sediment. Geol.). Our new estimates of sediment fluxes correlate positively with incompatible element concentrations in primitive arc lavas. We conclude that a large fraction of the local terrigenous sediments is subducted and contributes to the observed dichotomy in the trace element budget between primitive lavas from continental and oceanic margins.

Trace element and petrologic clues to the formation of forsterite-bearing Ca-Al-rich inclusions in the Allende meteorite

NASA Astrophysics Data System (ADS)

Wark, D. A.; Boynton, W. V.; Keays, R. R.; Palme, H.

1987-03-01

This work presents new trace element and petrographic data for three forsterite-bearing, Ca-Al-rich inclusions from the Allende meteorite: TE, 818a, and 110-A. Such inclusions form a continuum with Type B1 and B2 Ca-Al-rich inclusions (CAIs), and the authors refer to them as "Type B3" CAIs. Textures, mineral chemistries, crystal-chemically fractionated REE patterns, and other properties suggest that Type B3 crystallized from partly molten evaporative residues. They also present evidence that 818a was strongly re-heated and modified in the nebula after its initial crystallization: it consists of a core of coarse-grained Ti-Al-pyroxene (Tpx), forsterite, spinel and metal grains and a thick, surrounding mantle of melilite.

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.

Mineralogy and Geochemistry of Granitic rocks within Lichen Hills, Outback Nunatak, Northern Victoria Land, Antarctica

NASA Astrophysics Data System (ADS)

KIM, T.; KIM, Y.; Lee, I.; Lee, J.; Woo, J.

2015-12-01

The study areas, Lichen Hills and Outback Nunatak are located in the Northern Victoria Land which is close to Pacific Ocean side of Transantarctic Mountain (TAM), Antarctica. According to the study of Zeller and Dreschoff (1990), the radioactivity values of Lichen hills and Frontier Mt. area in the Victoria Land were very high. To identify the geochemical characteristics of granitic rocks in these areas, 13 samples of Lichen Hills rocks and 4 samples of Outback Nunatak rocks are analyzed. For mineralogical study, samples were observed in macroscale as well as microscale including microscope electron probe analysis. Rock samples of Lichen Hills, Outback Nunatak are mainly leucogranite and granitic pegmatite. These rock samples are composed of quartz, k-feldspar, plagioclase, muscovite, garnet, tourmaline like granite. In SEM-EDS analysis, the observed light colored minerals show relatively high Th, U, Dy, Ce, Nb concentration. This suggests that rock samples may contain minerals such as fergusonite, monazite, thorite, allanite, karnasurtite which are considered to be REE-bearing minerals. Samples of related rocks have been analyzed in terms of major, trace and rare earth element (REE) concentrations using X-ray fluorescence (XRF) spectrometer and Inductively Coupled Plasma Mass Spectrometer (ICP-MS). As concentration of SiO2 increase, Al2O3, TiO2, Fe2O3, MgO, P2O5 concentration decrease and Na2O, K2O, MnO concentration increase. Analyzed trace elements and REE are normalized using CI Chondrite, Primitive mantle. The normalized data show that LREE are enriched compared to HREE. The distinct negative anomalies of Eu, Sr are observed, indicating that rock-forming melts are fairly processed state of fractional crystallization. It means that Th, U, Nb, Ta are much enriched in the melts.

Geochemical evolution of Cenozoic-Cretaceous magmatism and its relation to tectonic setting, southwestern Idaho, U.S.A

NASA Technical Reports Server (NTRS)

Norman, Marc D.; Leeman, William P.

1989-01-01

The relationships between Cretaceous to Neogene magmatism and the tectonic setting of southwestern and central Idaho are evaluated. An overview of the tectonics and geology of the northwestern U.S. is presented. Major element, trace element, and Sr, Pb, and Nd isotopic data for the region are used to place constraints on magma source characteristics, the manner in which the magmatic sources evolved through time, and the nature of interactions among mantle and crustal domains in response to changing tectonic environment.

Mg-perovskite/silicate melt and magnesiowuestite/silicate melt partition coefficients for KLB-1 at 250 Kbars

NASA Technical Reports Server (NTRS)

Drake, Michael J.; Rubie, David C.; Mcfarlane, Elisabeth A.

1992-01-01

The partitioning of elements amongst lower mantle phases and silicate melts is of interest in unraveling the early thermal history of the Earth. Because of the technical difficulty in carrying out such measurements, only one direct set of measurements was reported previously, and these results as well as interpretations based on them have generated controversy. Here we report what are to our knowledge only the second set of directly measured trace element partition coefficients for a natural system (KLB-1).

Effects of sea-level changes on mid-ocean ridge magmatism and implications for emission rates of carbon.

NASA Astrophysics Data System (ADS)

Cerpa, N.; Katz, R. F.; Keller, T.

2017-12-01

Glacial cycles move water between ice sheets and the ocean, and hence cause regional pressure changes in the solid Earth. The rate of sea-level (SL) change during this cycle is comparable to the rate of mantle upwelling beneath mid-ocean ridges (MORs), and hence we expect the induced pressure variations to modify the rate and depth of silicate melting. SL variations may therefore induce changes in the supply and composition of magma at MORs, which could affect the flux of carbon into the climate system. Likewise, the trace-element geochemistry of magmas tapped by ridge volcanism may vary during these cycles due to variations in melt flux. Such variations may have been recorded by sediment-hosted volcanic glass fragments [Ferguson et al., 2017]. We investigate these questions using computational models of melt production and transport in which volatiles participate in the thermodynamics of melting. Published models of the effect of SL on MORs predict up to 10% variation in carbon emission rates for absolute changes in SL of 50-100 m with possible lag times of several tens of kyrs [Burley et al., 2015; Hasenclever et al., 2017]. A major assumption of those models is that water and carbon are passive, incompatible elements. But small concentrations of those volatiles affect the solidus of mantle peridotite and increase the volume of upper mantle undergoing partial melting. Hence the current predictions of variation in MOR carbon emission might be an underestimate. Moreover, published models neglect the effects of volatiles on melt transport. Recents studies have demonstrated that volatiles can induce channelized transport [Keller and Katz 2016], potentially affecting the rate at which carbon is extracted from the mantle. In this study, we investigate the interplay between SL variations, melting, and segregation of volatile-rich melts. We use two-phase magma/mantle dynamics coupled to melting models that treat water and carbon dioxide as thermodynamic components. We compare models of equilibrium and disequilibrium melting to assess the influence of reaction kinetics on magma productivity at MORs during SL variations. Our calculations provide new estimates of the lag and amplitude of carbon emissions during glacial cycles. We address the impact of SL variations on the trace-element composition of magmas.

Geology and geochemistry of newly discovered Tertiary carbonatite occurrences near Villa Ahumada area, Basin and Range province, Chihuahua, northern Mexico

NASA Astrophysics Data System (ADS)

Nandigam, Ravi Chenchu

This study targets some newly discovered carbonatite occurrences located in the eastern Mexican Basin and Range province, a few kilometers to the east of Villa Ahumada, Chihuahua. The region containing these occurrences experienced compression related to subduction of the Farallon plate until about 32 Ma that was followed by Basin and Range extension. Geological mapping (1:5,000 scale), petrography, study of drill hole cuttings and satellite images, and major and trace element chemical analyses were utilized to understand the intrusive style of the carbonatites, their mineralogy and petrogenesis. The carbonatites, named Yuca, Mariana and El Indio, collectively intrude limestones, granitic intrusives and subduction-related tuffs and lavas mainly as a stock, breccias and dikes. The Yuca carbonatite was emplaced as a 900-m diameter stock, 500 x 350 m breccia body, numerous dikes and networks of fracture fillings. Crosscutting field relationships at Yuca suggest at least two stages of carbonatite emplacement. At Mariana, carbonatite was emplaced as a 750 x 350 m breccia. Four out of nine reverse circulation drill holes penetrated and bottomed in the breccia at an average depth of about 300 m At El Indio, carbonatite was emplaced as a 20 m diameter breccia pipe and a 1m thick sill. Major minerals present are calcite, Fe-rich calcite and hematite. Sporadic presence of fluorite is common. At Mariana, two generations of grossular-rich garnets associated with limestones and granite porphyry respectively are recognized. It is inferred that garnets in granite porphyry represent metasomatic alteration due to the emplacement of carbonatite breccia. Parental magmas of Yuca carbonatites have undergone differentiation under low fO2 conditions during which they were progressively enriched in iron. The carbonatite compositional types recognized based on major element data, in the sequence of least to most highly differentiated, are (1) magnesio-, (2) calcio- and (3) ferrocarbonatites. The concentrations of thorium, uranium, niobium, yttrium and rare earth elements increase with differentiation. Carbonatites are associated with up to 20000 times enrichment of lanthanum and cerium with respect to chondrite. Finally, the Mariana carbonatite breccia is associated with about 7,928,550 short tons of rock with a grade of 0.14% SigmaREE, and primitive mantle normalized trace element plots of carbonatites indicate a mantle origin of their parental melts.

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.

The role and conditions of second-stage mantle melting in the generation of low-Ti tholeiites and boninites: the case of the Manihiki Plateau and the Troodos ophiolite

NASA Astrophysics Data System (ADS)

Golowin, Roman; Portnyagin, Maxim; Hoernle, Kaj; Sobolev, Alexander; Kuzmin, Dimitry; Werner, Reinhard

2017-12-01

High-Mg, low-Ti volcanic rocks from the Manihiki Plateau in the Western Pacific share many geochemical characteristics with subduction-related boninites such as high-Ca boninites from the Troodos ophiolite on Cyprus, which are believed to originate by hydrous re-melting of previously depleted mantle. In this paper we compare the Manihiki rocks and Troodos boninites using a new dataset on the major and trace element composition of whole rocks and glasses from these locations, and new high-precision, electron microprobe analyses of olivine and Cr-spinel in these rocks. Our results show that both low-Ti Manihiki rocks and Troodos boninites could originate by re-melting of a previously depleted lherzolite mantle source (20-25% of total melting with 8-10% melting during the first stage), as indicated by strong depletion of magmas in more to less incompatible elements (Sm/Yb < 0.8, Zr/Y < 2, Ti/V < 12) and high-Cr-spinel compositions (Cr# > 0.5). In comparison with Troodos boninites, the low-Ti Manihiki magmas had distinctively lower H2O contents (< 0.2 vs. > 2 wt% in boninites), 100 °C higher liquidus temperatures at a given olivine Fo-number, lower fO2 (ΔQFM < + 0.2 vs. ΔQFM > + 0.2) and originated from deeper and hotter mantle (1.4-1.7 GPa, 1440 °C vs. 0.8-1.0 GPa, 1300 °C for Troodos boninites). The data provide new evidence that re-melting of residual upper mantle is not only restricted to subduction zones, where it occurs under hydrous conditions, but can also take place due to interaction of previously depleted upper mantle with mantle plumes from the deep and hotter Earth interior.

Hyperextension of continental to oceanic-like lithosphere: The record of late gabbros in the shallow subcontinental lithospheric mantle of the westernmost Mediterranean

NASA Astrophysics Data System (ADS)

Hidas, Károly; Varas-Reus, Maria Isabel; Garrido, Carlos J.; Marchesi, Claudio; Acosta-Vigil, Antonio; Padrón-Navarta, José Alberto; Targuisti, Kamal; Konc, Zoltán

2015-05-01

We report gabbroic dikes in the plagioclase tectonite domains of the Ojén and Ronda massifs (Betic Cordillera, southern Spain), which record crystallization at low-pressure syn-, or slightly postkinematic to the late ductile history of the Betic Peridotite in the westernmost Mediterranean. We present mineral major and trace element compositional data of discordant gabbroic dikes in the Ojén massif and gabbroic patches in the Ronda massif, complemented by the whole rock and electron backscattered diffraction (EBSD) data of the Ojén occurrence. In the Ojén massif, gabbro occurs as 1-3 centimeter wide discordant dikes that crosscut the plagioclase tectonite foliation at high angle. These dikes are composed of cm-scale igneous plagioclase and clinopyroxene crystals that show shape preferred orientations subparallel to the lineation of the host peridotite and oblique to the trend of the dike. Intrusion of Ojén gabbro dikes is coherent with the stress field that formed the high temperature, ductile plagioclase tectonite foliation and then attests for a mantle igneous event prior to the intracrustal emplacement of the massif. In the Ronda massif, gabbroic rocks crystallized in subcentimeter wide anastomozing veins, or as interstitial patches in the host dunite. They are mostly composed of plagioclase and clinopyroxene. Plagioclase composition is bytownitic in the Ojén, and andesinic in the Ronda massif. Clinopyroxene in both places shows identical, light Rare-Earth Element (LREE) depleted trace element patterns. The calculated trace element composition of melts in exchange equilibrium with the studied igneous clinopyroxenes reflects LREE-enriched character coupled with negative Eu anomaly, and indicates that gabbro-forming melts in Ronda and Ojén share a common melt source with an island arc tholeiitic affinity. Geothermobarometric data and liquidus mineralogy indicate that gabbro crystallization occurred at shallow depths (0.2-0.5 GPa) in a 7-16 km thick lithospheric section. These data suggest that gabbro-forming melts in the Betic Peridotite record a mantle igneous event at very shallow depths and provide evidence for the hyperextension of the continental lithosphere compatible with extreme backarc basin extension induced by the slab rollback of the Cenozoic subduction system in the westernmost Mediterranean.

182W and HSE constraints from 2.7 Ga komatiites on the heterogeneous nature of the Archean mantle

NASA Astrophysics Data System (ADS)

Puchtel, Igor S.; Blichert-Toft, Janne; Touboul, Mathieu; Walker, Richard J.

2018-05-01

While the isotopically heterogeneous nature of the terrestrial mantle has long been established, the origin, scale, and longevity of the heterogeneities for different elements and isotopic systems are still debated. Here, we report Nd, Hf, W, and Os isotopic and highly siderophile element (HSE) abundance data for the Boston Creek komatiitic basalt lava flow (BCF) in the 2.7 Ga Abitibi greenstone belt, Canada. This lava flow is characterized by strong depletions in Al and heavy rare earth elements (REE), enrichments in light REE, and initial ε143Nd = +2.5 ± 0.2 and intial ε176Hf = +4.2 ± 0.9 indicative of derivation from a deep mantle source with time-integrated suprachondritic Sm/Nd and Lu/Hf ratios. The data plot on the terrestrial Nd-Hf array suggesting minimal involvement of early magma ocean processes in the fractionation of lithophile trace elements in the mantle source. This conclusion is supported by a mean μ142Nd = -3.8 ± 2.8 that is unresolvable from terrestrial standards. By contrast, the BCF exhibits a positive 182W anomaly (μ182W = +11.7 ± 4.5), yet is characterized by chondritic initial γ187Os = +0.1 ± 0.3 and low inferred source HSE abundances (35 ± 5% of those estimated for the present-day Bulk Silicate Earth, BSE). Collectively, these characteristics are unique among Archean komatiite systems studied so far. The deficit in the HSE, coupled with the chondritic Os isotopic composition, but a positive 182W anomaly, are best explained by derivation of the parental BCF magma from a mantle domain characterized by a predominance of HSE-deficient, differentiated late accreted material. According to the model presented here, the mantle domain that gave rise to the BCF received only ∼35% of the present-day HSE complement in the BSE before becoming isolated from the rest of the convecting mantle until the time of komatiite emplacement at 2.72 Ga. These new data provide strong evidence for a highly heterogeneous Archean mantle in terms of absolute HSE abundances and W isotopic composition, and also indicate slow mixing, on a timescale of at least 1.8 billion years. Additionally, the data are consistent with a stagnant-lid plate tectonic regime in the Hadean and Archean, prior to the onset of modern-style plate tectonics.

Enriched and depleted characters of the Amnay Ophiolite upper crustal section and the regionally heterogeneous nature of the South China Sea mantle

NASA Astrophysics Data System (ADS)

Perez, Americus d. C.; Faustino-Eslava, Decibel V.; Yumul, Graciano P.; Dimalanta, Carla B.; Tamayo, Rodolfo A.; Yang, Tsanyao Frank; Zhou, Mei-Fu

2013-03-01

The volcanic section of the Middle Oligocene Amnay Ophiolite in Mindoro, Philippines has previously been shown to be of normalmid-oceanic ridge basalt (NMORB) composition. Here we report for the first time an enriched mantle component that is additionally recorded in this crustal section. New whole rock major and trace element data are presented for nine mafic volcanic rocks from a section of the ophiolite that has not been previously examined. These moderately evolved tholeiitic basalts were found to have resulted from the bulk mixing of ˜10% ocean island basalt components with depleted mantle. Drawing together various geochemical characteristics reported for different rock suites taken as representatives of the South China Sea crust, including the enriched MORB (EMORB) and NMORB of the East Taiwan Ophiolite, the NMORB from previous studies of the Amnay Ophiolite and the younger ocean floor eruptives of the Scarborough Seamount-Reed Bank region, a veined mantle model is proposed for the South China Sea mantle. The NMORB magmatic products are suggested to have been derived from the more depleted portions of the mantle whereas the ocean island basalt (OIB) and EMORB-type materials from the mixing of depleted and veined/enriched mantle regions.

The Easternmost Southwest Indian Ridge: A Laboratory to Study MORB and Oceanic Gabbro Petrogenesis in a Very Low Melt Supply Context

NASA Astrophysics Data System (ADS)

Paquet, M.; Cannat, M.; Hamelin, C.; Brunelli, D.

2014-12-01

Our study area is located at the ultra-slow Southwest Indian Ridge, east of the Melville Fracture Zone, between 61 and 67°E. The melt distribution in this area is very heterogeneous, with corridors of ultramafic seafloor where plate separation is accommodated by large offset normal faults [Sauter, Cannat et al., 2013]. These ultramafic corridors also expose rare gabbros and basalts. We use the major and trace elements composition of these magmatic rocks to document the petrogenesis of MORB in this exceptionnally low melt supply portion of the MOR system. Basalts from the easternmost SWIR represent a global MORB end-member for major element compositions [Meyzen et al., 2003], with higher Na2O and Al2O3 wt%, and lower CaO and FeO wt% at a given MgO. Within this group, basalts from the ultramafic corridors have particularly high Na2O, low CaO and FeO wt%. Best fitting calculated liquid lines of descent are obtained for crystallization pressures of ~8 kbar. Gabbroic rocks recovered in the ultramafic corridors include gabbros, oxide-gabbros and variably impregnated peridotites. This presentation focuses on these impregnated samples, where cpx have high Mg#, yet are in equilibrium with the nearby basalts in terms of their trace element compositions. Plagioclase An contents vary over a broad range, and there is evidence for opx resorption. These characteristics result from melt-mantle interactions in the axial lithosphere, which may explain several peculiar major element characteristics of the basalts. Similar interactions probably occur beneath ridges at intermediate to slow and ultraslow spreading rates. We propose that they are particularly significant in our study area due to its exceptionnally low integrated melt-rock ratio.

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.

Evidence for a Meteoritic Component in Impact Melt Rock from the Chicxulub Structure

NASA Technical Reports Server (NTRS)

Koeberl, Christian; Sharpton, Virgil L.; Schuraytz, Benjamin C.; Shirey, Steven B.; Blum, Joel D.; Marin, Luis E.

1994-01-01

The Chicxulub structure in Yucatan, Mexico, has recently been recognized as a greater then 200-km-diameter multi-ring impact crater of K-T boundary age. Crystalline impact melt rocks and breccias from within the crater, which have compositions similar to those of normal continental crustal rocks and which show shock metamorphic effects, have been studied for trace element and Re-Os isotope compositions. Re-Os isotope systematics allow the sensitive and selective determination of an extraterrestrial component in impact-derived rocks. A melt rock sample shows elevated iridium concentrations, an osmium concentration of 25 ppb, and a low Os-187/Os-188 ratio of 0.113, which are incompatible with derivation from the continental crust. Even though the Os-187/Os-188 ratio is slightly lower than the range so far measured in meteorites, a mantle origin seems unlikely for mass balance reasons and because the cratering event is unlikely to have excavated mantle material. The data support the hypothesis of a heterogeneously distributed meteoritic component in the Chicxulub melt rock. A sample of impact glass from the Haitian K-T boundary at Beloc yielded about 0.1 ppb osmium and an Os-187/0s-188 ratio of 0.251, indicating the presence of a small meteoritic component in the impact ejecta as well.

Amphibole incongruent melting under Lithospheric Mantle conditions in spinel peridotites from Balaton area, Hungary

NASA Astrophysics Data System (ADS)

Ntaflos, Theodoros; Abart, Rainer; Bizimis, Michel

2017-04-01

Pliocene alkali basalts from the western Pannonian Basin carry mantle xenoliths comprising hydrous and anhydrous spinel peridotites. We studied coarse and fine grained fertile to depleted spinel lherzolites, spinel harzubrgites and dunites from Szentbékálla, Balaton, in detail, using XRF, EPMA and LA-ICP-MS and MC-ICP-MS techniques. Pliocene alkali basalts containing mantle xenoliths with three major types of textures are widespread in the studied area: fine-grained primary and secondary equigranular, coarse-grained protogranular and transitional between equigranular and protogranular textures. Melt pockets, are common in the studied xenoliths. The shape of several melt pockets resembles euhedral amphibole. Other samples have thin films of intergranular glass attributed to the host basalt infiltration. Calculations have shown that such xenoliths experienced an up to 2.4% host basalt infiltration. The bulk rock Al2O3 and CaO concentrations vary from 0.75 to 4.1 and from 0.9 to 3.6 wt% respectively, and represent residues after variable degrees of partial melting. Using bulk rock major element abundances, the estimated degree of partial melting ranges from 4 to 20%.. The Primitive Mantle normalized clinopyroxene trace element abundances reveal a complicated evolution of the Lithospheric mantle underneath Balaton, which range from partial melting to modal and cryptic metasomatism. Subduction-related melt/fluids and/or infiltration of percolating undersaturated melts could be account for the metasomatic processes. The radiogenic isotopes of Sr, Nd and Hf in clinopyroxene suggest that this metasomatism was a relatively recent event. Textural evidence suggests that the calcite filling up the vesicles in the melt pockets and in veinlets cross-cutting the constituent minerals is of epigenetic nature and not due to carbonatite metasomatism. Mass balance calculations have shown that the bulk composition of the melt pockets is identical to small amphibole relics found as inclusions in second generation clinopyroxene within the melt pockets. Evidently the melt pockets represent amphibole, which have been incongruently molten. The necessary heat for the amphibole breakdown was derived from the host basalt. The estimated time for diffusive Ca exchange between matrix olivine and olivine overgrowth in contact with the melt pockets is very short, ranging between 21 and 200 days, indicating that amphibole breakdown took place immediately before or during the xenolith entrainment in the alkali basalt.

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.

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.

An introduction of Markov chain Monte Carlo method to geochemical inverse problems: Reading melting parameters from REE abundances in abyssal peridotites

NASA Astrophysics Data System (ADS)

Liu, Boda; Liang, Yan

2017-04-01

Markov chain Monte Carlo (MCMC) simulation is a powerful statistical method in solving inverse problems that arise from a wide range of applications. In Earth sciences applications of MCMC simulations are primarily in the field of geophysics. The purpose of this study is to introduce MCMC methods to geochemical inverse problems related to trace element fractionation during mantle melting. MCMC methods have several advantages over least squares methods in deciphering melting processes from trace element abundances in basalts and mantle rocks. Here we use an MCMC method to invert for extent of melting, fraction of melt present during melting, and extent of chemical disequilibrium between the melt and residual solid from REE abundances in clinopyroxene in abyssal peridotites from Mid-Atlantic Ridge, Central Indian Ridge, Southwest Indian Ridge, Lena Trough, and American-Antarctic Ridge. We consider two melting models: one with exact analytical solution and the other without. We solve the latter numerically in a chain of melting models according to the Metropolis-Hastings algorithm. The probability distribution of inverted melting parameters depends on assumptions of the physical model, knowledge of mantle source composition, and constraints from the REE data. Results from MCMC inversion are consistent with and provide more reliable uncertainty estimates than results based on nonlinear least squares inversion. We show that chemical disequilibrium is likely to play an important role in fractionating LREE in residual peridotites during partial melting beneath mid-ocean ridge spreading centers. MCMC simulation is well suited for more complicated but physically more realistic melting problems that do not have analytical solutions.

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).

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.

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.

Geochemistry and geochronology of the ∼0.82 Ga high-Mg gabbroic dykes from the Quanji Massif, southeast Tarim Block, NW China: Implications for the Rodinia supercontinent assembly

NASA Astrophysics Data System (ADS)

Liao, Fanxi; Wang, Qinyan; Chen, Nengsong; Santosh, M.; Xu, Yixian; Mustafa, Hassan Abdelsalam

2018-05-01

The role of the Tarim Block in the reconstruction of the Neoproterozoic supercontinent Rodinia remains contentious. Here we report a suite of high-Mg gabbroic dykes from the Yingfeng area in northwestern Quanji Massif, which is considered as a fragment of the Tarim Block in NW China. Magmatic zircons from these dykes yield to have a weighted mean 206Pb/238U age of 822.2 ± 5.3 Ma, recording the timing of their emplacement. The gabbros have high MgO (9.91-13.09 wt%), Mg numbers (69.89-75.73) and CaO (8.41-13.55 wt%), medium FeOt (8.50-9.67 wt%) and TiO2 (0.67-0.93 wt%), variable Al2O3 (13.04-16.07 wt%), and high Cr (346.14-675.25 ppm), but relatively low Ni (138.72-212.94 ppm), suggestive of derivation from a primary magma. The rocks display chondrite-normalized LREE patterns with weak fractionation but flat HREE patterns relative to those of the N-MORB. Their primitive mantle normalized trace elemental patterns show positive Rb, Ba and U but negative Th, Nb, Ti and Zr anomalies, carrying characteristics of both mid-ocean ridge basalts and arc basalts. The εHf(t) values of the zircons from these rocks vary from +4.7 to +13.5 with depleted mantle model ages (TDM) of 1.23-0.85 Ga, and the youngest value nearly approaching that for the coeval depleted mantle, suggesting significant addition of juvenile materials. Our data suggest that the strongly depleted basaltic magma was probably sourced from a depleted mantle source that had undergone metasomatism by subduction-related components in a back-arc setting. Accordingly we postulate that a subduction-related tectonic regime possibly prevailed at ∼0.8 Ga along the southeastern margin of the Tarim Block. Combining with available information from the northern Tarim Block, we propose an opposite verging double-sided subduction model for coeval subduction of the oceanic crust beneath both the southern and northern margins of the Tarim Block during early Neoproterozoic.

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.

Young Prehistoric Kilauea Lava Flows From Uwekahuna Bluff, Hawaii: Mixed Source or Hybrid Magmas?

NASA Astrophysics Data System (ADS)

Marske, J. P.; Pietruszka, A. J.; Garcia, M. O.; Norman, M. D.; Rhodes, J. M.

2004-12-01

For the last 350 kyr, nearly the entire known compositional range of subaerial and submarine Kilauea lavas lie within the range defined by the volcano's historical eruptions. In contrast, Rhodes et al. (1989) discovered that some Kilauea lavas have Mauna Loa-like major-and trace-element signatures and concluded that Mauna Loa magmas may periodically invade Kilauea's shallow plumbing system. Here, we present new major- and trace- element data for 25 sequential prehistoric lava flows (0.5 to <2 ka) from the upper 55 m of the north wall of Kilauea caldera at Uwekahuna Bluff (UB). Although historical Kilauea and Mauna Loa lavas have been compositionally distinct for most of the last 230 kyr, our results show that the UB lavas span the geochemical spectrum between these neighboring volcanoes. At a given MgO content, the abundances of major elements (e.g., SiO2, TiO2, or CaO) in the UB lavas typically plot between historical Mauna Loa and Kilauea values, suggesting that these lavas originated from compositionally intermediate parental magmas or from hybridization between historical Kilauea- and Mauna Loa-type magmas. In contrast to the major element abundances, ratios of highly to moderately incompatible elements (e.g., Nb/Y) in the UB lavas are mostly Mauna Loa-like. These incompatible trace element ratios reveal a rapid fluctuation of Kilauea's lava composition since prehistoric times: (1) two lava flows at the base of the suite record a decrease in Nb/Y from historical Kilauea- to historical Mauna Loa-type values, (2) a weathered hiatus near the middle of the flow sequence coincides with a gradual Nb/Y minimum and reversal, and (3) the top three lava flows transition back into historical Kilauea-type Nb/Y values with a smooth temporal connection to the oldest historical lavas from this volcano. The systematic variations of these UB trace-element ratios may result from gradual mixing between Kilauea- and Mauna Loa-type magmas within the summit reservoir and/or varying degrees of partial melting of a Mauna Loa-like mantle heterogeneity within Kilauea's source region. Highly incompatible element ratios (e.g., Rb/Nb), which are typically unaffected by variable melt fraction, indicate that changes in the degree of partial melting alone cannot explain these Mauna Loa-like lava flows. Pb, Sr and Nd isotopic ratios of the Uwekahuna Bluff lavas will be presented to differentiate mantle source and melting effects from magma chamber processes.

Melt focusing and geochemical evolution at mid-ocean ridges: simulations of reactive two-phase flow

NASA Astrophysics Data System (ADS)

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

2017-12-01

The geochemical character of MORB and related off-axis volcanic products reflects the signature of chemical reservoirs in the mantle, the processes of melt transport from source to surface, or both. Focusing of partial melt to the ridge axis controls the proportion of deep, volatile- and incompatible-rich melts that contribute to MORB formation. However, the effect of volatiles, including CO2 and H2O, on melt segregation and focusing remains poorly understood. We investigate this transport using 2-D numerical simulations of reactive two-phase flow. The phases are solid mantle and liquid magma. Major elements and volatiles are represented by a system with 4 or 6 pseudo-components. This captures 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]. Trace element transport is computed for 5 idealized elements between highly incompatible and compatible behavior. Our results indicate that volatiles cause channelized melt transport, which leads to fluctuations in volume and composition of melt focused to the axis. The volatile-induced expansion of the melting regime at depth, however, has no influence on melt focusing. Up to 50% of deep, volatile-rich melts are not focused to the axis, but are emplaced along the oceanic LAB. There, crystallization of accumulated melt leads to enrichment of volatiles and incompatibles in the deep lithosphere. This has implications for volatile recycling by subduction, seismic properties of the oceanic LAB, and potential sources for seamount volcanism. Results from a suite of simulations, constrained by catalogued observational data [4,5,6], enable prediction of global MORB and volatile output and systematic variations of major, volatile and trace element concentrations as a function of mantle conditions and dynamic properties. 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.

Geochemical and Mineralogical Profiles Across the Listvenite- Metamorphic Transition in the Basal Megathrust of the Oman Ophiolite: First Results from Drilling at Oman Drilling Project Hole BT1B

NASA Astrophysics Data System (ADS)

Godard, M.; Bennett, E.; Carter, E.; Kourim, F.; Lafay, R.; Noël, J.; Kelemen, P. B.; Michibayashi, K.; Harris, M.

2017-12-01

The transition from the base of the Oman ophiolite to the underlying metamorphic sole was drilled at Hole BT1B (Sumail Massif) during Phase 1 of Oman Drilling Project (Winter 2016-2017). 74 samples were collected from the 300m of recovered cores for whole rock geochemical and XRD analyses. 55 listvenites, ophicarbonates and serpentinites, and 19 schists and greenstones were analyzed for major and minor elements (XRF) and for CO2 and S concentrations (CHNS) aboard DV Chikyu (ChikyuOman, Summer 2017). Analyses for trace elements (ICP-MS) at the University of Montpellier are in progress. The composition of listvenites, ophicalcites and serpentinites recovered at Hole BT1B record extensive interactions between CO2-rich fluids and the serpentinized peridotites. These reactions involved addition of SiO2 and formation of carbonates at the expense of the serpentinized peridotite protolith. All samples recovered from the mantle section are enriched in fluid mobile and incompatible trace elements compared to the mean composition of the Oman mantle. These enrichments are up to 103 times the Oman mantle for Rb and Ba. They mimic the pattern of the samples from the metamorphic sole. This suggests that the composition of the listvenites in these elements is controlled by that of contaminating fluids that may have originated in the same lithologies as those drilled at the base of Hole BT1B. Listvenites, ophicalcites and serpentinites also show notable downhole chemical variations, with listvenites showing marked variations in Al2O3 and TiO2. Occurrence of lherzolites and cpx-harzburgites has been reported at the base of the Oman dominantly harzburgitic mantle section. The observed variations in the listvenites (Al2O3 and TiO2) could be related to the composition of their protolith, the deepest having more fertile compositions. Alternatively, the observed downhole changes in the composition of listvenites may relate to the progressive equilibration of the reacting ultramafic-rocks and/or listvenite with the fluids originating in the subducting metamorphic sole; these variations could be related to heterogeneous reaction kinetics (temperature, reactive surfaces, chemical gradients) and/or to transport (e.g. local variations in permeability) within the listvenite units.

Hf-Nd isotope constraints on the origin of the Cretaceous Caribbean plateau and its relationship to the Galápagos plume

NASA Astrophysics Data System (ADS)

Thompson, P. M. E.; Kempton, P. D.; White, R. V.; Kerr, A. C.; Tarney, J.; Saunders, A. D.; Fitton, J. G.; McBirney, A.

2004-01-01

Formation of the Cretaceous Caribbean plateau, including the komatiites of Gorgona, has been linked to the currently active Galápagos hotspot. We use Hf-Nd isotopes and trace element data to characterise both the Caribbean plateau and the Galápagos hotspot, and to investigate the relationship between them. Four geochemical components are identified in the Galápagos mantle plume: two 'enriched' components with ɛHf and ɛNd similar to enriched components observed in other mantle plumes, one moderately enriched component with high Nb/Y, and a fourth component which most likely represents depleted MORB source mantle. The Caribbean plateau basalt data form a linear array in Hf-Nd isotope space, consistent with mixing between two mantle components. Combined Hf-Nd-Pb-Sr-He isotope and trace element data from this study and the literature suggest that the more enriched Caribbean end member corresponds to one or both of the enriched components identified on Galápagos. Likewise, the depleted end member of the array is geochemically indistinguishable from MORB and corresponds to the depleted component of the Galápagos system. Enriched basalts from Gorgona partially overlap with the Caribbean plateau array in ɛHf vs. ɛNd, whereas depleted basalts, picrites and komatiites from Gorgona have a high ɛHf for a given ɛNd, defining a high- ɛHf depleted end member that is not observed elsewhere within the Caribbean plateau sequences. This component is similar, however, in terms of Hf-Nd-Pb-He isotopes and trace elements to the depleted plume component recognised in basalts from Iceland and along the Reykjanes Ridge. We suggest that the Caribbean plateau represents the initial outpourings of the ancestral Galápagos plume. Absence of a moderately enriched, high Nb/Y component in the older Caribbean plateau (but found today on the island of Floreana) is either due to changing source compositions of the plume over its 90 Ma history, or is an artifact of limited sampling. The high- ɛHf depleted component sampled by the Gorgona komatiites and depleted basalts is unique to Gorgona and is not found in the Caribbean plateau. This may be an indication of the scale of heterogeneity of the Caribbean plateau system; alternatively Gorgona may represent a separate oceanic plateau derived from a completely different Pacific plume, such as the Sala y Gomez.

Petrogenesis and tectonic association of rift-related basic Panjal dykes from the northern Indian plate, North-Western Pakistan: evidence of high-Ti basalts analogous to dykes from Tibet

NASA Astrophysics Data System (ADS)

Sajid, Muhammad; Andersen, Jens; Arif, Mohammad

2017-10-01

Rift related magmatism during Permian time in the northern margin of Indian plate is represented by basic dykes in several Himalayan terranes including north western Pakistan. The field relations, mineralogy and whole rock geochemistry of these basic dykes reveal significant textural, mineralogical and chemical variation between two major types (a) dolerite and (b) amphibolite. Intra-plate tectonic settings for both rock types have been interpreted on the basis of low Zr/Nb ratios (< 10), K/Ba ratios (20-40) and Hf-Ta-Th and FeO-MgO-Al2O3 discrimination diagrams. The compositional zoning in plagioclase and clinopyroxene, variation in olivine compositions and major elements oxide trends indicate a vital role of fractional crystallization in the evolution of dolerites, which also show depletion in rare earth elements (REEs) and other incompatible elements compared to the amphibolites. The equilibrium partial melting models from primitive mantle using Dy/Yb, La/Yb, Sm/Yb and La/Sm ratios show that amphibolite formed by smaller degrees (< 5%) of partial melting than the dolerites (< 10%). The trace elements ratios suggest the origination of dolerites from the subcontinental lithospheric mantle with some crustal contamination. This is consistent with a petrogenetic relationship with Panjal trap magmatism, reported from Kashmir and other parts of north western India. The amphibolites, in contrast, show affinity towards Ocean Island basalts (OIB) with a relatively deep asthenospheric mantle source and minimal crustal contribution and are geochemically similar to the High-Ti mafic dykes of southern Qiangtang, Tibet. These similarities combined with Permian tectonic restoration of Gondwana indicate the coeval origin for both dykes from distinct mantle source during continental rifting related to formation of the Neotethys Ocean.

Petrogenesis and tectonic association of rift-related basic Panjal dykes from the northern Indian plate, North-Western Pakistan: evidence of high-Ti basalts analogous to dykes from Tibet

NASA Astrophysics Data System (ADS)

Sajid, Muhammad; Andersen, Jens; Arif, Mohammad

2018-06-01

Rift related magmatism during Permian time in the northern margin of Indian plate is represented by basic dykes in several Himalayan terranes including north western Pakistan. The field relations, mineralogy and whole rock geochemistry of these basic dykes reveal significant textural, mineralogical and chemical variation between two major types (a) dolerite and (b) amphibolite. Intra-plate tectonic settings for both rock types have been interpreted on the basis of low Zr/Nb ratios (< 10), K/Ba ratios (20-40) and Hf-Ta-Th and FeO-MgO-Al2O3 discrimination diagrams. The compositional zoning in plagioclase and clinopyroxene, variation in olivine compositions and major elements oxide trends indicate a vital role of fractional crystallization in the evolution of dolerites, which also show depletion in rare earth elements (REEs) and other incompatible elements compared to the amphibolites. The equilibrium partial melting models from primitive mantle using Dy/Yb, La/Yb, Sm/Yb and La/Sm ratios show that amphibolite formed by smaller degrees (< 5%) of partial melting than the dolerites (< 10%). The trace elements ratios suggest the origination of dolerites from the subcontinental lithospheric mantle with some crustal contamination. This is consistent with a petrogenetic relationship with Panjal trap magmatism, reported from Kashmir and other parts of north western India. The amphibolites, in contrast, show affinity towards Ocean Island basalts (OIB) with a relatively deep asthenospheric mantle source and minimal crustal contribution and are geochemically similar to the High-Ti mafic dykes of southern Qiangtang, Tibet. These similarities combined with Permian tectonic restoration of Gondwana indicate the coeval origin for both dykes from distinct mantle source during continental rifting related to formation of the Neotethys Ocean.

Geochemical and Re-Os isotope constraints on the origin and age of the Songshugou peridotite massif in the Qinling orogen, central China

NASA Astrophysics Data System (ADS)

Nie, Hu; Yang, Jianzhou; Zhou, Guangyan; Liu, Chuanzhou; Zheng, Jianping; Zhang, Wen-Xiang; Zhao, Yu-Jie; Wang, Hao; Wu, Yuanbao

2017-11-01

The Songshugou peridotite massif in the Qinling orogenic belt is one of the largest orogenic spinel peridotite bodies in central China, but its origin remains controversial and its age is poorly constrained. We have carried out an integrated study of major and trace element composition, mineral chemistry, platinum group elements (PGE), as well as Re-Os isotope systematics of 1 harzburgite and 12 dunites from the Songshugou peridotite massif. These samples contain high Mg# olivine (90.0-91.3) and Cr# spinel (83.4-96.0). The harzburgite and dunites are characterized by relatively low whole-rock Al2O3 (0.32-0.60 wt.%), CaO (0.26-1.57 wt.%), and Na2O (0.07-0.12 wt.%) concentrations. The studied samples have very low concentrations of middle and heavy rare earth elements and exhibit enrichments in iridium-group platinum-group elements (IPGE) relative to palladium-group PGE. The Songshugou peridotites exhibit variable enrichments of light rare earth elements, large ion lithophile elements, Re, Zr, and Hf, which resulted from reactions with melt after their isolation from the convecting mantle. Combined with previous results, our data suggest that the Songshugou peridotites are highly refractory mantle residues derived from a forearc mantle wedge. 187Os/188Os values of the studied samples vary from 0.12073 to 0.12390, and 187Re/188Os ratios are 0.005-0.081. The average Re-Os model ages (TMA) and maximum Re depletion model age (TRD) of the Songshugou peridotites are ca. 1.2-1.1 Ga, suggesting a tectonic affinity to the South China Block and that the peridotites formed during the assembly of the Rodinia supercontinent. The Songshugou peridotites were sourced from a mantle wedge above a subduction zone, and finally incorporated into the underlying continental lithosphere by exhumation.

Paradoxical co-existing base metal sulphides in the mantle: The multi-event record preserved in Loch Roag peridotite xenoliths, North Atlantic Craton

NASA Astrophysics Data System (ADS)

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

2017-04-01

The role of the subcontinental lithospheric mantle as a source of precious metals for mafic magmas is contentious and, given the chalcophile (and siderophile) character of metals such as the platinum-group elements (PGE), Se, Te, Re, Cu and Au, the mobility of these metals is intimately linked with that of sulphur. Hence the nature of the host phase(s), and their age and stability in the subcontinental lithospheric mantle may be of critical importance. We investigate the sulphide mineralogy and sulphide in situ trace element compositions in base metal sulphides (BMS) in a suite of spinel lherzolite mantle xenoliths from northwest Scotland (Loch Roag, Isle of Lewis). This area is situated on the margin of the North Atlantic Craton which has been overprinted by a Palaeoproterozoic orogenic belt, and occurs in a region which has undergone magmatic events from the Palaeoproterozoic to the Eocene. We identify two populations of co-existing BMS within a single spinel lherzolite xenolith (LR80) and which can also be recognised in the peridotite xenolith suite as a whole. Both populations consist of a mixture of Fe-Ni-Cu sulphide minerals, and we distinguished between these according to BMS texture, petrographic setting (i.e., location within the xenolith in terms of 'interstitial' or within feldspar-spinel symplectites, as demonstrated by X-ray Computed Microtomography) and in situ trace element composition. Group A BMS are coarse, metasomatic, have low concentrations of total PGE (< 40 ppm) and high (Re/Os)N (ranging 1 to 400). Group B BMS strictly occur within symplectites of spinel and feldspar, are finer-grained rounded droplets, with micron-scale PtS (cooperite), high overall total PGE concentrations (15-800 ppm) and low (Re/Os)N ranging 0.04 to 2. Group B BMS sometimes coexist with apatite, and both the Group B BMS and apatite can preserve rounded micron-scale Ca-carbonate inclusions indicative of sulphide-carbonate-phosphate immiscibility. This carbonate-phosphate metasomatic association appears to be important in forming PGE-rich sulphide liquids, although the precise mechanism for this remains obscure. As a consequence of their position within the symplectites, Group B BMS are particularly vulnerable to being incorporated in ascending mantle-derived magmas (either by melting or physical entrainment). Based on the cross-cutting relationships of the symplectites, it is possible to infer the relative ages of each metasomatic BMS population. We tally these with major tectono-magmatic events for the North Atlantic region by making comparisons to carbonatite events recorded in crustal and mantle rocks, and we suggest that the Pt-enrichment was associated with a pre-Carboniferous carbonatite episode. This method of mantle xenolith base metal sulphide documentation may ultimately permit the temporal and spatial mapping of the chalcophile metallogenic budget of the lithospheric mantle, providing a blueprint for assessing regional metallogenic potential.

Mantle to Surface Fluid Transfer Above a Flat Slab Subduction Zone: Isotopic Evidence from Hot Springs in the Cordillera Blanca, Peru

NASA Astrophysics Data System (ADS)

Newell, D. L.; Jessup, M. J.; Hilton, D. R.; Shaw, C. A.; Hughes, C. A.

2015-12-01

Thermal springs in the Cordillera Blanca, Peru, provide geochemical evidence for deeply circulated hydrothermal fluids that carry significant mantle-derived helium. The Cordillera Blanca is a ~200 km-long NNW-SSE trending mountain range in the Peruvian Andes located above an amagmatic flat-slab subduction segment. The west side of the range is bounded by the Cordillera Blanca detachment that preserves a progression of top to the west ductile shear to brittle normal faulting since ~5 Ma. We report aqueous and stable isotope geochemical results from fluid and gas samples collected in 2013 and 2015 from 13 hot springs emanating from the Cordillera Blanca detachment and associated hanging wall faults. Most springs are vigorously bubbling (degassing), and range in temperature, pH, and conductivity from 17-89 °C, 5.95-8.87, and 0.17-21.5 mS, respectively. The hottest springs issue directly from the northern segment of the detachment. Geochemically, springs are CO2-rich, alkaline-chloride to alkaline-carbonate waters, with elevated trace metal contents including Fe, Cu, As, Zn, Sb, and Tl. Notably, As contents are ≤11 ppm, indicating that thermal waters may be adversely impacting local water quality. Water δ18O and δD, trends in elemental chemistry, and cation geothermometry collectively demonstrate mixing of hot (200-260 °C) saline fluid with cold meteoric recharge along the fault. Helium isotope ratios (3He/4He) for dissolved gases in the hot springs range from 0.62 to 1.98 RC/RA, indicating the presence of ~25% mantle-derived helium, assuming mixing of an asthenospheric end-member with the crustal helium reservoir. CO2/3He and carbon stable isotope ratios indicate a carbon source derived from mixing of crustal sources with minor mantle carbon. Overall, the volatile signature overlaps with orogen-wide datasets where crustal overprinting has modified mantle contributions at active arc volcanoes. Given the long duration since active magmatism in the Cordillera Blanca region, we suggest that mantle helium was mobilized from the continental mantle-lithosphere by metasomatic fluids derived from slab dehydration. These spring data thus reveal a mantle to surface connection and highlight the role of detachment faults in compressional orogens for fluid transfer in the crust.

Experimental determination of carbon partitioning between upper mantle minerals and silicate melts: initial results and comparison to trace element partitioning (Nb, Rb, Ba, U, Th, K)

NASA Astrophysics Data System (ADS)

Rosenthal, A.; Hauri, E. H.; Hirschmann, M. M.; Davis, F. A.; Withers, A. C.; Fogel, M. L.

2012-12-01

Inventories of C in the mantle and magmatic fluxes of C between the mantle and the Earth's outer envelopes are poorly constrained in part owing to challenges in determining undegassed C concentrations of pristine basalts. Saal et al. [1] proposed that the behavior of Nb could be used as a proxy for C, owing to apparently similar behavior of the two elements in Siqueiros Transform MORB, but higher C/Nb ratios in popping rocks [2] call into question the applicability of the C/Nb proxy. Here, we present experimentally determined carbon partition coefficients (D's) between nominally volatile-free mantle minerals (olivine, OL; orthopyroxene, OPX; clinopyroxene, CPX; garnet, GA) and melts at 0.8-3 GPa, and 1250-1500°C. We conducted piston-cylinder experiments using an olivine-tholeiite + 4 wt% CO2, doped with Nb, Rb, U, Th, and 13C to enhance detection limits. To promote growth of crystals big enough for SIMS analyses, experiments were either long (<6 days), or at an initial higher temperature (T) before cooling slowly to a target T. We also produced SIMS calibration glass standards with varying amounts of C, and subject to ongoing analyses. We analyzed carbon (12C, 13C), H, F, and trace elements (Nb, Rb, Ba, U, Th, K) of both mineral phases and quenched liquids in subsets of experimental runs (21 in graphite-lined Pt-capsules, 6 in Fe-doped Pt-lined capsules) using both Cameca IMS 6F and NanoSIMS instruments. D's measured for 12C and 13C are close to 5x10-4, in most cases D13C>D12C, but a few have the opposite. Continuous exchange of the liquid (initially rich in 13C) with the graphite capsules (rich in 12C) may yield D's with 13C>12C. D's with 12C>13C are likely owing to either low count rates or comparatively high analytical contamination. Concentrations in minerals vary from 0.20-3.46 ppm for C, 25-176 ppm for H2O, and 0.05-1.21 ppm for F, whereas liquids tend to much higher values (C≤0.9 wt%; H2O≤1.5 wt%; F≤34 ppm; P≤0.25 wt%; S≤43 ppm; Cl≤77 ppm). Resulting D's indicate that C is highly incompatible in all major mantle mineral phases, with D's for OL, OPX and CPX of close to 5x10-4, and for GA ~2.2x10-4. D's for H2O (2x10-4 to ~3x10-2) and F (~2.3x10-3 to ~5.8x10-2) are comparable to those found in previous studies. Trace element partition determinations are in progress, but comparison to previous studies indicates that carbon is significantly more incompatible during mantle melting than Nb, U, or Th, and has behavior approximately similar to Ba. We therefore suggest that undegassed C/Ba ratios may be useful indicators of C fluxes and concentrations in basalt source regions where very low degrees of melting might fractionate C/Nb ratios. [1] Saal, A, Hauri, EH, Langmuir, CH, Perfit, M (2002) Nature 419, 451-455. [2] Cartigny, P, Pineau, F, Aubaud, C, Javoy, M (2008) Earth Planet Sci Lett 265, 672-685.

The Quaternary calc-alkaline volcanism of the Patagonian Andes close to the Chile triple junction: geochemistry and petrogenesis of volcanic rocks from the Cay and Maca volcanoes (˜45°S, Chile)

NASA Astrophysics Data System (ADS)

D'Orazio, M.; Innocenti, F.; Manetti, P.; Tamponi, M.; Tonarini, S.; González-Ferrán, O.; Lahsen, A.; Omarini, R.

2003-08-01

Major- and trace-element, Sr-Nd isotopes, and mineral chemistry data were obtained for a collection of volcanic rock samples erupted by the Cay and Maca Quaternary volcanoes, Patagonian Andes (˜45°S, Chile). Cay and Maca are two large, adjacent stratovolcanoes that rise from the Chiloe block at the southern end of the southern volcanic zone (SVZ) of the Andes. Samples from the two volcanoes are typical medium-K, calc-alkaline rocks that form two roughly continuous, largely overlapping series from subalkaline basalt to dacite. The overall geochemistry of the samples studied is very similar to that observed for most volcanoes from the southern SVZ. The narrow range of Sr-Nd isotope compositions ( 87Sr/ 86Sr=0.70389-0.70431 and 143Nd/ 144Nd=0.51277-0.51284) and the major- and trace-element distributions indicate that the Cay and Maca magmas differentiated by crystal fractionation without significant contribution by crustal contamination. This is in accordance with the thin (<30 km), relatively young (Paleozoic or more recent) continental crust beneath the volcanoes. The nature of the subduction-derived materials involved in the genesis of the Cay and Maca magmas is investigated by means of the relative concentration of fluid mobile (e.g. Ba) and fluid immobile (e.g. Nb, Ta, Zr, Y) elements and other relevant trace-element ratios (e.g. Sr/Y). The results indicate that small amounts (<1 wt%) of both subducted sediments and slab-released fluids were added to the mantle sources of the Cay and Maca volcanoes and that, despite the very young age (<10 Ma) of the oceanic lithosphere subducted beneath the volcanoes, slab melts were not involved in the magma genesis. Notwithstanding the proximity of the Cay and Maca magma sources to the northern edge of the slab window generated by the subduction of the Chile ridge under the South American plate, we did not find any geochemical evidence for a contribution of a subslab asthenospheric mantle. However, this mantle has been used to explain the peculiar geochemical features (e.g. the mild alkalinity and relatively low ratios between large ion lithophile and high field strength elements) of the Hudson volcano, which is located even closer to the slab window than the Cay and Maca volcanoes are.

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.

Dynamic melting in plume heads: the formation of Gorgona komatiites and basalts

NASA Astrophysics Data System (ADS)

Arndt, Nicholas T.; Kerr, Andrew C.; Tarney, John

1997-01-01

The small Pacific island of Gorgona, off the coast of Colombia, is well known for its spectacular spinifex-textured komatiites. These high-Mg liquids, which have been linked to a late Cretaceous deep mantle plume, are part of a volcanic series with a wide range of trace-element compositions, from moderately enriched basalts ( La/SmN ˜ 1.5) to extremely depleted ultramafic tuffs and picrites ( La/SmN ˜ 0.2). Neither fractional crystallization, nor partial melting of a homogeneous mantle source, can account for this large variation: the source must have been chemically heterogeneous. Low 143Nd/144Nd in the more enriched basalts indicates some initial source heterogeneity but most of the variation in magma compositions is believed to result from dynamic melting during the ascent of a plume. Modelling of major- and trace-element compositions suggests that ultramafic magmas formed at ˜ 60-100 km depth, and that the melt extraction that gave rise to their depleted sources started at still greater depths. The ultra-depleted lavas represent magmas derived directly from the hottest, most depleted parts of the plume; the more abundant moderately depleted basalts are interpreted as the products of pooling of liquids from throughout the melting region.

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.

Trace elements in magnetite as petrogenetic indicators

NASA Astrophysics Data System (ADS)

Dare, Sarah A. S.; Barnes, Sarah-Jane; Beaudoin, Georges; Méric, Julien; Boutroy, Emilie; Potvin-Doucet, Christophe

2014-10-01

We have characterized the distribution of 25 trace elements in magnetite (Mg, Al, Si, P, Ca, Sc, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Ga, Ge, Y, Zr, Nb, Mo, Sn, Hf, Ta, W, and Pb), using laser ablation ICP-MS and electron microprobe, from a variety of magmatic and hydrothermal ore-forming environments and compared them with data from the literature. We propose a new multielement diagram, normalized to bulk continental crust, designed to emphasize the partitioning behavior of trace elements between magnetite, the melt/fluid, and co-crystallizing phases. The normalized pattern of magnetite reflects the composition of the melt/fluid, which in both magmatic and hydrothermal systems varies with temperature. Thus, it is possible to distinguish magnetite formed at different degrees of crystal fractionation in both silicate and sulfide melts. The crystallization of ilmenite or sulfide before magnetite is recorded as a marked depletion in Ti or Cu, respectively. The chemical signature of hydrothermal magnetite is distinct being depleted in elements that are relatively immobile during alteration and commonly enriched in elements that are highly incompatible into magnetite (e.g., Si and Ca). Magnetite formed from low-temperature fluids has the lowest overall abundance of trace elements due to their lower solubility. Chemical zonation of magnetite is rare but occurs in some hydrothermal deposits where laser mapping reveals oscillatory zoning, which records the changing conditions and composition of the fluid during magnetite growth. This new way of plotting all 25 trace elements on 1 diagram, normalized to bulk continental crust and elements in order of compatibility into magnetite, provides a tool to help understand the processes that control partitioning of a full suit of trace elements in magnetite and aid discrimination of magnetite formed in different environments. It has applications in both petrogenetic and provenance studies, such as in the exploration of ore deposits and in sedimentology.

Tectonic origin of serpentinites on Syros, Greece: Geochemical signatures of abyssal origin preserved in a HP/LT subduction complex

NASA Astrophysics Data System (ADS)

Cooperdock, Emily H. G.; Raia, Natalie H.; Barnes, Jaime D.; Stockli, Daniel F.; Schwarzenbach, Esther M.

2018-01-01

This study combines whole rock trace and major element geochemistry, and stable isotope (δD and δ18O) analyses with petrographic observations to deduce the origin and tectonic setting of serpentinization of ultramafic blocks from the exhumed HP/LT Aegean subduction complex on Syros, Greece. Samples are completely serpentinized and are characterized by mineral assemblages that consist of variable amounts of serpentine, talc, chlorite, and magnetite. δD and δ18O values of bulk rock serpentinite powders and chips (δD = - 64 to - 33‰ and δ18O = + 5.2 to + 9.0‰) reflect hydration by seawater at temperatures < 250 °C in an oceanic setting pre-subduction, or by fluids derived from dehydrating altered oceanic crust during subduction. Fluid-mobile elements corroborate the possibility of initial serpentinization by seawater, followed by secondary fluid-rock interactions with a sedimentary source pre- or syn-subduction. Whole rock major element, trace element, and REE analyses record limited melt extraction, exhibit flat REE patterns, and do not show pronounced Eu anomalies. The geochemical signatures preserved in these serpentinites argue against a mantle wedge source, as has been previously speculated for ultramafic rocks on Syros. Rather, the data are consistent with derivation from abyssal peridotites in a hyper-extended margin setting or mid-ocean ridge and fracture zone environment. In either case, the data suggest an extensional and/or oceanic origin associated with the Cretaceous opening of the Pindos Ocean and not a subduction-related derivation from the mantle wedge.

Changes in magma storage conditions following caldera collapse at Okataina Volcanic Center, New Zealand

DOE Office of Scientific and Technical Information (OSTI.GOV)

Rubin, Allison; Cooper, Kari M.; Leever, Marissa

Large silicic volcanic centers produce both small rhyolitic eruptions and catastrophic caldera-forming eruptions. Although changes in trace element and isotopic compositions within eruptions following caldera collapse have been observed at rhyolitic volcanic centers such as Yellowstone and Long Valley, much still remains unknown about the ways in which magma reservoirs are affected by caldera collapse. We present 238U– 230Th age, trace element, and Hf isotopic data from individual zircon crystals from four eruptions from the Okataina Volcanic Center, Taupo Volcanic Zone, New Zealand, in order to assess changes in trace element and isotopic composition of the reservoir following the 45-kamore » caldera-forming Rotoiti eruption. Our data indicate that (1) mixing of magmas derived from crustal melts and mantle melts takes place within the shallow reservoir; (2) while the basic processes of melt generation likely did not change significantly between pre- and post-caldera rhyolites, post-caldera zircons show increased trace element and isotopic heterogeneity that suggests a decrease in the degree of interconnectedness of the liquid within the reservoir following collapse; and (3) post-caldera eruptions from different vents indicate different storage times of the amalgamated melt prior to eruption. Furthermore, these data further suggest that the timescales needed to generate large volumes of eruptible melt may depend on the timescales needed to increase interconnectedness and achieve widespread homogenization throughout the reservoir.« less

Changes in magma storage conditions following caldera collapse at Okataina Volcanic Center, New Zealand

DOE PAGES

Rubin, Allison; Cooper, Kari M.; Leever, Marissa; ...

2015-12-15

Large silicic volcanic centers produce both small rhyolitic eruptions and catastrophic caldera-forming eruptions. Although changes in trace element and isotopic compositions within eruptions following caldera collapse have been observed at rhyolitic volcanic centers such as Yellowstone and Long Valley, much still remains unknown about the ways in which magma reservoirs are affected by caldera collapse. We present 238U– 230Th age, trace element, and Hf isotopic data from individual zircon crystals from four eruptions from the Okataina Volcanic Center, Taupo Volcanic Zone, New Zealand, in order to assess changes in trace element and isotopic composition of the reservoir following the 45-kamore » caldera-forming Rotoiti eruption. Our data indicate that (1) mixing of magmas derived from crustal melts and mantle melts takes place within the shallow reservoir; (2) while the basic processes of melt generation likely did not change significantly between pre- and post-caldera rhyolites, post-caldera zircons show increased trace element and isotopic heterogeneity that suggests a decrease in the degree of interconnectedness of the liquid within the reservoir following collapse; and (3) post-caldera eruptions from different vents indicate different storage times of the amalgamated melt prior to eruption. Furthermore, these data further suggest that the timescales needed to generate large volumes of eruptible melt may depend on the timescales needed to increase interconnectedness and achieve widespread homogenization throughout the reservoir.« less

Origin and mixing timescale of Earth's late veneer

NASA Astrophysics Data System (ADS)

Prescher, C.; Allu Peddinti, D.; Bell, E. A.; Bello, L.; Cernok, A.; Ghosh, N.; Tucker, J.; Wielicki, M. M.; Zahnle, K. J.

2012-12-01

Experimental studies on the partitioning behavior of highly siderophile elements (HSE) between silicate and metallic melts imply that the Earth's mantle should have been highly depleted in these elements by core formation in an early magma ocean. However, present HSE contents of the Earth's mantle are ~3 orders of magnitude higher than that expected by experiments. The apparent over-abundance of HSE has commonly been explained by the addition of meteoritic material in the "late veneer" which describes the exogenous mass addition following the moon forming impact and concluding with the late heavy bombardment at ~3.8-3.9 Ga. The strongest evidence for this theory is that the platinum group element (PGE) contents in today's mantle are present in chondritic relative abundances, as opposed to a fractionated pattern expected with metal-silicate partitioning. Archean komatiites indicate that the PGE content of the Earth's mantle increased from about half their present abundances at 3.5 Ga to their present abundances at 2.9 Ga. This secular increase in PGE content suggests a progressive mixing of the late veneer material into the Earth's mantle. However, this time scale also implies that the whole mantle was relatively well mixed by 2.9 Ga. We use a compilation of existing isotopic and trace element data in order to constrain the origin and composition of the late veneer. We use PGE abundances, W abundances and W isotopic compositions in chondritic meteorites and the primitive upper mantle to compute the amount of mass delivered during the late veneer and find the late veneer mass to be ~0.6 % the mass of the bulk silicate Earth (consistent with earlier estimates). We also use the 187Re-187Os and 190Pt-186Os systems to constrain the composition and timing of delivery of the impacting population. We model the efficiency of mantle mixing in this time frame by using 3-dimensional numerical geodynamical simulations and geochemical constraints. Initial parameters include the amount of mass delivered in the late veneer and the Archean internal heating which is at least 4 times higher than the present values, due to the higher abundance of radioactive elements. Another important parameter is the mechanism of mass addition to the Earth. We test three end-member scenarios: (1) a single very large impactor accounting for the entire mass addition, (2) sprinkling of a large number of small impactors over the whole Earth which then mix into the mantle, or (3) by using a size/frequency distribution estimated from the lunar cratering record and corrected for the difference in gravitational cross section of the Earth and the Moon. This project results from collaborations begun at the CIDER II workshop held at KITP, UCSB, 2012.

Marine Carbonate Component in the Mantle Beneath the Southeastern Tibetan Plateau: Evidence From Magnesium and Calcium Isotopes

NASA Astrophysics Data System (ADS)

Liu, Fang; Li, Xin; Wang, Guiqin; Liu, Yufei; Zhu, Hongli; Kang, Jinting; Huang, Fang; Sun, Weidong; Xia, Xiaoping; Zhang, Zhaofeng

2017-12-01

Tracing and identifying recycled carbonates is a key issue to reconstruct the deep carbon cycle. To better understand carbonate subduction and recycling beneath the southeastern Tibetan Plateau, high-K cal-alkaline volcanic rocks including trachy-basalts and trachy-andesites from Tengchong were studied using Mg and Ca isotopes. The low δ26Mg (-0.31 ± 0.03‰ to -0.38 ± 0.03‰) and δ44/40Ca (0.67 ± 0.07‰ to 0.80 ± 0.04‰) values of these volcanic rocks compared to those of the mantle (-0.25 ± 0.07‰ and 0.94 ± 0.05‰, respectively) indicate the incorporation of isotopically light materials into the mantle source, which may be carbonate-bearing sediments with low δ26Mg and δ44/40Ca values. In addition, no correlations of δ26Mg and δ44/40Ca with either SiO2 contents or trace element abundance ratios (e.g., Sm/Yb and Ba/Y) were observed, suggesting that limited Mg and Ca isotopic fractionation occurred during cal-alkaline magmatic differentiation. A binary mixing model using Mg-Ca isotopes shows that 5-8% carbonates dominated primarily by dolostone were recycled back into the mantle. Since Tengchong volcanism is still active and probably related to ongoing plate tectonic movement, we propose that the recycled carbonates are derived from oceanic crust related to the ongoing subduction of the Indian plate.

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.

Water and Metasomatism in the Slave Cratonic Lithosphere (Canada): An FTIR Study

NASA Technical Reports Server (NTRS)

Kilgore, McKensie; Peslier, Anne H.; Brandon, Alan D.; Schaffer, Lillian Aurora; Pearson, D. Graham; O'Reilly, Suzanne Yvette; Kopylova, Maya G.; Griffin, William L.

2017-01-01

Water in the mantle influences melting, viscosity, seismic velocity, and electrical conductivity. The role played by water in the long-term stabilization of cratonic roots is currently being debated. This study focuses on water contents of mantle minerals (olivine, pyroxene and garnet) from xenoliths found in kimberlites of the Archean Slave craton. 19 mantle xenoliths from central Lac de Gras, and 10 from northern Jericho were analyzed by FTIR for water, and their equilibration depths span the several compositional layers identified beneath the region. At both locations, the shallow peridotites have lower water contents in their olivines (11-30 ppm H2O) than those from the deeper layers (28-300 ppm H2O). The driest olivines, however, are not at the base of the cratonic lithosphere (>6 GPa) as in the Kaapvaal craton. Instead, the deepest olivines are hydrous (31-72 ppm H2O at Lac de Gras and 275 ppm H2O at Jericho). Correlations of water in clinopyroxene and garnet with their other trace element contents are consistent with water being added by metasomatism by melts resembling kimberlite precursors in the mantle approx.0.35 Ga ago beneath Lac de Gras. The northern Jericho xenoliths are derived from a region of the Slave craton that is even more chemically stratified, and was affected at depth by the 1.27 Ga Mackenzie igneous events. Metasomatism at Jericho may be responsible for the particularly high olivine water contents (up to 300 ppm H2O) compared to those at Lac de Gras, which will be investigated by acquiring trace-element data on these xenoliths. These data indicate that several episodes of metasomatic rehydration occurred in the deep part of the Slave craton mantle lithosphere, with the process being more intense in the northern part beneath Jericho, likely related to a translithospheric suture serving as a channel to introduce fluids and/or melts in the northern region. Consequently, rehydration of the lithosphere does not necessarily cause cratonic root delamination and these peridotites may represent localized metasomatic zones - the wall rocks to kimberlite magma passage.

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.

Orogenic, Ophiolitic, and Abyssal Peridotites

NASA Astrophysics Data System (ADS)

Bodinier, J.-L.; Godard, M.

2003-12-01

"Tectonically emplaced" mantle rocks include subcontinental, suboceanic, and subarc mantle rocks that were tectonically exhumed from the upper mantle and occur:(i) as dispersed ultramafic bodies, a few meters to kilometers in size, in suture zones and mountain belts (i.e., the "alpine," or "orogenic" peridotite massifs - De Roever (1957), Thayer (1960), Den Tex (1969));(ii) as the lower ultramafic section of large (tens of kilometers) ophiolite or island arc complexes, obducted on continental margins (e.g., the Oman Ophiolite and the Kohistan Arc Complex - Coleman (1971), Boudier and Coleman (1981), Burg et al. (1998));(iii) exhumed above the sea level in ocean basins (e.g., Zabargad Island in the Red Sea, St. Paul's islets in the Atlantic and Macquarie Island in the southwestern Pacific - Tilley (1947), Melson et al. (1967), Varne and Rubenach (1972), Bonatti et al. (1981)).The "abyssal peridotites" are samples from the oceanic mantle that were dredged on the ocean floor, or recovered from drill cores (e.g., Bonatti et al., 1974; Prinz et al., 1976; Hamlyn and Bonatti, 1980).Altogether, tectonically emplaced and abyssal mantle rocks provide insights into upper mantle compositions and processes that are complementary to the information conveyed by mantle xenoliths (See Chapter 2.05). They provide coverage to vast regions of the Earth's upper mantle that are sparsely sampled by mantle xenoliths, particularly in the ocean basins and beneath passive continental margins, back-arc basins, and oceanic island arcs.Compared with mantle xenoliths, a disadvantage of some tectonically emplaced mantle rocks for representing mantle compositions is that their original geodynamic setting is not exactly known and their significance is sometimes a subject of speculation. For instance, the provenance of orogenic lherzolite massifs (subcontinental lithosphere versus upwelling asthenosphere) is still debated (Menzies and Dupuy, 1991, and references herein), as is the original setting of ophiolites (mid-ocean ridges versus supra-subduction settings - e.g., Nicolas, 1989). In addition, the mantle structures and mineralogical compositions of tectonically emplaced mantle rocks may be obscured by deformation and metamorphic recrystallization during shallow upwelling, exhumation, and tectonic emplacement. Metamorphic processes range from high-temperature recrystallization in the stability field of plagioclase peridotites ( Rampone et al., 1993) to complete serpentinization (e.g., Burkhard and O'Neill, 1988). Some garnet peridotites record even more complex evolutions. They were first buried to, at least, the stability field of garnet peridotites, and, in some cases to greater than 150 km depths ( Dobrzhinetskaya et al., 1996; Green et al., 1997; Liou, 1999). Then, they were exhumed to the surface, dragged by buoyant crustal rocks ( Brueckner and Medaris, 2000).Alternatively, several peridotite massifs are sufficiently well preserved to allow the observation of structural relationships between mantle lithologies that are larger than the sampling scale of mantle xenoliths. It is possible in these massifs to evaluate the scale of mantle heterogeneities and the relative timing of mantle processes such as vein injection, melt-rock reaction, deformation, etc… Detailed studies of orogenic and ophiolitic peridotites on centimeter- to kilometer-scale provide invaluable insights into melt transfer mechanisms, such as melt flow in lithospheric vein conduits and wall-rock reactions (Bodinier et al., 1990), melt extraction from mantle sources via channeled porous flow ( Kelemen et al., 1995) or propagation of kilometer-scale melting fronts associated with thermalerosion of lithospheric mantle ( Lenoir et al., 2001). In contrast, mantle xenoliths may be used to infer either much smaller- or much larger-scale mantle heterogeneities, such as micro-inclusions in minerals ( Schiano and Clocchiatti, 1994) or lateral variations between lithospheric provinces ( O'Reilly et al., 2001).The abyssal peridotites are generally strongly affected by oceanic hydrothermal alteration. Most often, their whole-rock compositions are strongly modified and cannot be used straightforwardly to assess mantle compositions (e.g., Baker and Beckett, 1999). However, even in the worst cases the samples generally contain fresh, relic minerals (mainly clinopyroxene) that represent the only available direct information on the oceanic upper mantle in large ocean basins, away from hot-spot volcanic centers. In situ trace-element data on clinopyroxenes from abyssal peridotites provide constraints on melting processes at mid-ocean ridges (Johnson et al., 1990).In this chapter, we review the main inferences on upper mantle composition and heterogeneity that may be drawn from geochemical analyses of the major elements, lithophile trace elements, and Nd-Sr isotopes in tectonically emplaced and abyssal mantle rocks. In addition we emphasize important insights into the mechanisms of melt/fluid transfer that can be deduced from detailed studies of these mantle materials.

Devonian magmatism in the Timan Range, Arctic Russia - subduction, post-orogenic extension, or rifting?

NASA Astrophysics Data System (ADS)

Pease, V.; Scarrow, J. H.; Silva, I. G. Nobre; Cambeses, A.

2016-11-01

Devonian mafic magmatism of the northern East European Craton (EEC) has been variously linked to Uralian subduction, post-orogenic extension associated with Caledonian collision, and rifting. New elemental and isotopic analyses of Devonian basalts from the Timan Range and Kanin Peninsula, Russia, in the northern EEC constrain magma genesis, mantle source(s) and the tectonic process(es) associated with this Devonian volcanism to a rift-related context. Two compositional groups of low-K2O tholeiitic basalts are recognized. On the basis of Th concentrations, LREE concentrations, and (LREE/HREE)N, the data suggest two distinct magma batches. Incompatible trace elements ratios (e.g., Th/Yb, Nb/Th, Nb/La) together with Nd and Pb isotopes indicate involvement of an NMORB to EMORB 'transitional' mantle component mixed with variable amounts of a continental component. The magmas were derived from a source that developed high (U,Th)/Pb, U/Th and Sm/Nd over time. The geochemistry of Timan-Kanin basalts supports the hypothesis that the genesis of Devonian basaltic magmatism in the region resulted from local melting of transitional mantle and lower crust during rifting of a mainly non-volcanic continental rifted margin.

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).

Aluminum, iron, lead, cadmium, copper, zinc, chromium, magnesium, strontium, and calcium content in bone of end-stage renal failure patients.

PubMed

D'Haese, P C; Couttenye, M M; Lamberts, L V; Elseviers, M M; Goodman, W G; Schrooten, I; Cabrera, W E; De Broe, M E

1999-09-01

Little is known about trace metal alterations in the bones of dialysis patients or whether particular types of renal osteodystrophy are associated with either increased or decreased skeletal concentrations of trace elements. Because these patients are at risk for alterations of trace elements as well as for morbidity from skeletal disorders, we measured trace elements in bone of patients with end-stage renal disease. We analyzed bone biopsies of 100 end-stage renal failure patients enrolled in a hemodialysis program. The trace metal contents of bone biopsies with histological features of either osteomalacia, adynamic bone disease, mixed lesion, normal histology, or hyperparathyroidism were compared with each other and with the trace metal contents of bone of subjects with normal renal function. Trace metals were measured by atomic absorption spectrometry. The concentrations of aluminum, chromium, and cadmium were increased in bone of end-stage renal failure patients. Comparing the trace metal/calcium ratio, significantly higher values were found for the bone chromium/calcium, aluminum/calcium, zinc/calcium, magnesium/calcium, and strontium/calcium ratios. Among types of renal osteodystrophy, increased bone aluminum, lead, and strontium concentrations and strontium/calcium and aluminum/calcium ratios were found in dialysis patients with osteomalacia vs the other types of renal osteodystrophy considered as one group. Moreover, the concentrations of several trace elements in bone were significantly correlated with each other. Bone aluminum was correlated with the time on dialysis, whereas bone iron, aluminum, magnesium, and strontium tended to be associated with patient age. Bone trace metal concentrations did not depend on vitamin D intake nor on the patients' gender. The concentration of several trace elements in bone of end-stage renal failure patients is disturbed, and some of the trace metals under study might share pathways of absorption, distribution, and accumulation. The clinical significance of the increased/decreased concentrations of several trace elements other than aluminum in bone of dialysis patients deserves further investigation.

Petrogenesis of basaltic volcanic rocks from the Pribilof Islands, Alaska, by melting of metasomatically enriched depleted lithosphere, crystallization differentiation, and magma mixing

USGS Publications Warehouse

Chang, J.M.; Feeley, T.C.; Deraps, M.R.

2009-01-01

The Pribilof Islands, Alaska, are located in the Bering Sea in a continental intraplate setting. In this study we examine the petrology and geochemistry of volcanic rocks from St. Paul (0??54-0??003 Ma) and St. George (2??8-1??4 Ma) Islands, the two largest Pribilof Islands. Rocks from St. George can be divided into three groups: group 1 is a high-MgO, low-SiO. 2 suite composed primarily of basanites; group 2 is a high-MgO, high-SiO 2 suite consisting predominantly of alkali basalts; group 3 is an intermediate- to low-MgO suite that includes plagioclase-phyric subalkali basalts and hawaiites. Major and trace element geochemistry suggests that groups 1 and 2 formed by small-degree partial melting of amphibole-bearing to amphibole-free garnet peridotite. Group 1 rocks were the earliest melts produced from the most hydrous parts of the mantle, as they show the strongest geochemical signature of amphibole in their source. The suite of rocks from St. Paul ranges from 14??4 to 4??2 wt % MgO at relatively constant SiO 2 contents (43??1-47??3 wt %). The most primitive St. Paul rocks are modeled as mixtures between magmas with compositions similar to groups 1 and 2 from St. George Island, which subsequently fractionated olivine, clinopyroxene, and spinel to form more evolved rocks. Plagioclase-phyric group 3 rocks from St. George are modeled as mixtures between an evolved melt similar to the evolved magmas on St. Paul and a fractionated group 2 end-member from St. George. Mantle potential temperatures estimated for primitive basanites and alkali basalts are ???1400??C and are similar to those of mid-ocean ridge basalts (MORB). Similarly, 87Sr/. 86Sr and 143Nd/. 144Nd values for all rocks are MORB-like, in the range of 0??702704-0??703035 and 0??513026-0??513109, respectively. 208Pb/. 204Pb vs 206Pb/. 204Pb values lie near the MORB end-member but show a linear trend towards HIMU (high time-integrated 238U/. 204Pb). Despite isotopic similarities to MORB, many of the major and trace element characteristics are similar to those of ocean island basalts (OIB), including enrichment in alkalis and incompatible trace elements. These characteristics are interpreted to indicate that their mantle source experienced an ancient melt-removal event that is reflected in depleted radiogenic isotopic compositions and was then re-enriched by metasomatism that elevated incompatible trace element contents, but was too young to produce a time-integrated change in radiogenic isotopic ratios. Evidence suggests that the Pribilof Island basalts did not form in either a plume or a back-arc basin tectonic setting. Rather, they were produced by melting of metasomatically hydrated upper mantle peridotite at relatively low temperatures and were able to erupt at the surface through extensional or transtensional faults that served as conduits for the magmas. ?? The Author 2009. Published by Oxford University Press.

Seventh Annual V. M. Goldschmidt Conference

NASA Technical Reports Server (NTRS)

1997-01-01

Topics considered include: Subduction of the Aseismic Cocos Ridge Displaced Magma Sources Beneath the Cordillera de Talamanca, Costa Rica; Topography of Transition Zone Discontinuities: A Measure of 'Olivine' Content and Evidence for Deep Cratonic Roots; Uranium Enrichment in Lithospheric Mantle: Case Studies from French Massif Central; Rare-Earth-Element Anomalies in the Decollement Zone of the nankai Accretionary Prism, Japan: Evidence of Fluid Flow?; Rare Earth Elements in Japanese Mudrocks: The Influence of Provenance; The Evolution of Seawater Strontium Isotopes in the Last Hundred Million Years: Reinterpretation and Consequences for Erosion and Climate Models; From Pat to Tats: The Lead Isotope Legacy in the Studies of the Continental Crust-Upper Mantle System; Geochronology of the Jack Hills Detrital Zircons by Precise Uranium-Lead Isotope-Dilution Analysis of Crystal Fragments; Iridium in the Oceans; The Helium-Heat-Lead Paradox; Control of Distribution Patterns of Heavy Metals in Ganga Plain Around Kanpur Region, India, by Fluvial Geomorphic Domains; Geochemical and Isotopic Features of Ferrar Magmatic Provience (Victoria Land, Antarctica); Rare Earth Elements in Marine Fine-Grained Sediments from the Northwestern Portuguese Shelf (Atlantic); Aspects of Arc Fluxes; General Kinetic Model for Dolomite Precipitation Rate with Application to the Secular History of Seawater Composition; High-Precision Uranium-series Chronology from Speleothems; Trace-Element Modeling of Aqueous Fluid-Peridotite Interaction in the Mantle Wedge of Subduction Zones; Rainfall Variations in Southeastern Australia over the Last 500,000 Years from Speleothem Deposition; The Role of Water in High-Pressure Fluids; The Kinetic Conditions of Metamorphic Minearogenesis: Evidence from Minerals and Assemblages.

Sub-Moho Reflectors, Mantle Faults and Lithospheric Rheology

NASA Astrophysics Data System (ADS)

Brown, L. D.

2013-12-01

One of the most unexpected and dramatic observations from the early years of deep reflection profiling of the continents using multichannel CMP techniques was the existing of prominent reflections from the upper mantle. The first of these, the Flannan thrust/fault/feature, was traced by marine profiling of the continental margin offshore Britain by the BIRPS program, which soon found them to be but one of several clear sub-crustal discontinuities in that area. Subsequently, similar mantle reflectors have been observed in many areas around the world, most commonly beneath Precambrian cratonic areas. Many, but not all, of these mantle reflections appear to arise from near the overlying Moho or within the lower crust before dipping well into the mantle. Others occur as subhorizontal events at various depths with the mantle, with one suite seeming to cluster at a depth of about 75 km. The dipping events have been variously interpreted as mantle roots of crustal normal faults or the deep extension of crustal thrust faults. The most common interpretation, however, is that these dipping events are the relicts of ancient subduction zones, the stumps of now detached Benioff zones long since reclaimed by the deeper mantle. In addition to the BIRPS reflectors, the best known examples include those beneath Fennoscandia in northern Europe, the Abitibi-Grenville of eastern Canada, and the Slave Province of northwestern Canada (e.g. on the SNORCLE profile). The most recently reported example is from beneath the Sichuan Basin of central China. The preservation of these coherent, and relatively delicate appearing, features beneath older continental crust and presumably within equally old (of not older) mantle lithosphere, has profound implications for the history and rheology of the lithosphere in these areas. If they represent, as widely believe, some form of faulting with the lithosphere, they provide corollary constraints on the nature of faulting in both the lower crust and upper mantle. The SNORCLE mantle reflectors, which can be traced deep within the early Precambrian (?) mantle by both surface (controlled source) reflection profiles and passive (receiver function) images most clearly illustrates the rheological implications of such feature. The SNORCLE events appear to root upwards into the lower crust and extend to depths approaching 200 km into the mantle. This would seem to require the preservation of undeformed mantle lithosphere for almost 2.5 billion years in this area. This preservation is clearly inconsistent with the interpretation of nearby shallower mantle interfaces as marking the modern lithosphere-asthenosphere boundary. In summary, dipping mantle reflections imply preservation of substantial thicknesses of mantle lithosphere for very long periods of time, and localization of mantle deformation during the formation of these structures along relatively narrow, discrete interfaces rather than across broad zones of diffuse deformation. .

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.

Water contents of clinopyroxenes from sub-arc mantle peridotites

USGS Publications Warehouse

Turner, Michael; Turner, Simon; Blatter, Dawnika; Maury, Rene; Perfit, Michael; Yogodzinski, Gene

2017-01-01

One poorly constrained reservoir of the Earth's water budget is that of clinopyroxene in metasomatised, mantle peridotites. This study presents reconnaissance Sensitive High-Resolution, Ion Microprobe–Stable Isotope (SHRIMP–SI) determinations of the H2O contents of (dominantly) clinopyroxenes in rare mantle xenoliths from four different subduction zones, i.e. Mexico, Kamchatka, Philippines, and New Britain (Tabar-Feni island chain) as well as one intra-plate setting (western Victoria). All of the sub-arc xenoliths have been metasomatised and carry strong arc trace element signatures. Average measured H2O contents of the pyroxenes range from 70 ppm to 510 ppm whereas calculated bulk H2O contents range from 88 ppm to 3 737 ppm if the variable presence of amphibole is taken into account. In contrast, the intra-plate, continental mantle xenolith from western Victoria has higher water contents (3 447 ppm) but was metasomatised by alkali and/or carbonatitic melts and does not carry a subduction-related signature. Material similar to the sub-arc peridotites can either be accreted to the base of the lithosphere or potentially be transported by convection deeper into the mantle where it will lose water due to amphibole breakdown.

Highly siderophile element constraints on the genesis of Azorean lavas

NASA Astrophysics Data System (ADS)

Waters, C. L.; Watanabe, S.; Olson, K. M.; Walker, R. J.; Widom, E.; Hanan, B. B.; Day, J. M.

2013-12-01

Ocean island basalts (OIB) from the Azores archipelago show incompatible element and Sr-Nd-Hf-Pb isotopic heterogeneity both among different islands and within individual islands. This heterogeneity has commonly been attributed to the presence of a mantle plume delivering diverse recycled materials--including terrigenous sediments, metasomatized subcontinental lithosphere, and oceanic crust--to the melting region beneath the Azores (Turner et al., 1997; Widom and Shirey, 1996; Beier et al., 2007). Despite an abundance of datasets including major and trace element and Sr, Nd, Hf, and Pb isotopic compositions, the origin of elemental and isotopic heterogeneity in the Azores remains vigorously debated. We report new highly siderophile element (HSE: Os, Ir, Pd, Pt, Ru, Re) abundance data alongside major and trace element abundance and Nd-Hf-Os-Pb isotope data for a suite of high MgO (8-17 wt%) lavas from the islands of Sao Miguel, Pico, Faial, and Terceira. These lavas span most of the range of incompatible trace element and Nd-Hf-Pb isotopic heterogeneity observed for the Azores. Because HSEs are largely controlled by sulfide, they provide an alternative to the classic perspective of OIB petrogenesis derived from lithophile elements. The results show distinct fractionation patterns for HSEs from different islands at a similar range of MgO contents. Lavas from Pico and Faial have lower absolute HSE abundances (total HSE abundances ~0.001 × CI chondrite; Ir=0.014-0.133 ppb) and are generally more homogeneous than lavas from Terceira and Sao Miguel (total HSE = ~0.003 × CI chondrite; Ir=0.038-0.657 ppb)). Faial and Pico lavas (IrN* = 0.8×0.3, where IrN* = IrN/[(OsN+RuN)0.5] x 100) also commonly lack the positive relative enrichment in Ir observed in Terceira and Sao Miguel lavas (IrN* = 2.4 ×1.1). In contrast to previous studies of OIB in which HSEs are observed to positively correlate with MgO (e.g., Day, 2013), only Re correlates with MgO, as expected given its moderate incompatibility in silicate systems. All other HSEs show wide variability at similar MgO, broadly correlate with each other, yet do not correlate with Nd-Hf-Pb isotope compositions. Thus, we interpret HSE variability to reflect variations in mantle sulfide source composition and sulfide melting beneath different islands in the Azores hotspot.

Geochemical evidence for airborne dust additions to soils in Channel Islands National Park, California

USGS Publications Warehouse

Muhs, D.R.; Budahn, J.R.; Johnson, D.L.; Reheis, M.; Beann, J.; Skipp, G.; Fisher, E.; Jones, J.A.

2008-01-01

There is an increasing awareness that dust plays important roles in climate change, biogeochemical cycles, nutrient supply to ecosystems, and soil formation. In Channel Islands National Park, California, soils are clay-rich Vertisols or Alfisols and Mollisols with vertic properties. The soils are overlain by silt-rich mantles that contrast sharply with the underlying clay-rich horizons. Silt mantles contain minerals that are rare or absent in the volcanic rocks that dominate these islands. Immobile trace elements (Sc-Th-La and Ta-Nd-Cr) and rare-earth elements show that the basalt and andesite on the islands have a composition intermediate between upper-continental crust and oceanic crust. In contrast, the silt fractions and, to a lesser extent, clay fractions of the silt mantle have compositions closer to average upper-continental crust and very similar to Mojave Desert dust. Island shelves, exposed during the last glacial period, could have provided a source of eolian sediment for the silt mantles, but this is not supported by mineralogical data. We hypothesize that a more likely source for the silt-rich mantles is airborne dust from mainland California and Baja California, either from the Mojave Desert or from the continental shelf during glacial low stands of sea. Although average winds are from the northwest in coastal California, easterly winds occur numerous times of the year when "Santa Ana" conditions prevail, caused by a high-pressure cell centered over the Great Basin. The eolian silt mantles constitute an important medium of plant growth and provide evidence that abundant eolian silt and clay may be delivered to the eastern Pacific Ocean from inland desert sources. ?? 2007 Geological Society of America.

Interpretation of trace element and isotope features of basalts: relevance of field relations, petrology, major element data, phase equilibria, and magma chamber modeling in basalt petrogenesis

NASA Astrophysics Data System (ADS)

O'Hara, M. J.; Herzberg, C.

2002-06-01

The concentrations and ratios of the major elements determine the physical properties and the phase equilibria behavior of peridotites and basalts in response to the changing energy contents of the systems. The behavior of the trace elements and isotopic features are influenced in their turn by the phase equilibria, by the physical character of the partial melting and partial crystallization processes, and by the way in which a magma interacts with its wall rocks. Concentrating on the trace element and isotope contents of basalts to the exclusion of the field relations, petrology, major element data, and phase equilibria is as improvident as slaughtering the buffalo for the sake of its tongue. The crust is a cool boundary layer and a density filter, which impedes the upward transfer of hot, dense "primary" picritic and komatiitic liquids. Planetary crusts are sites of large-scale contamination and extensive partial crystallization of primitive melts striving to escape to the surface. Escape of truly unmodified primitive melts to the surface is a rare event, requiring the resolution of daunting problems in chemical and mechanical engineering. Primary status for volumetrically abundant basalts such as mid-ocean ridge basalt, ocean island basalt, and continental flood basalts is denied by their low-pressure cotectic character, first remarked upon on petrological grounds in 1928 and on experimental grounds in 1962. These basalt liquids are products of crystal-liquid separation at low pressure. Primary status for these common basalts is further denied by the phase equilibria of such compositions at elevated pressures, when the required residual mantle mineralogy (magnesian olivine and orthopyroxene) is not stable at the liquidus. It is also denied by the picritic or komatiitic nature of partial melts of candidate upper-mantle compositions at high pressures - a conclusion supported by calculation of the melt composition, which would need to be extracted in order to explain the chemical variation between fertile and residual peridotite in natural ultramafic rock suites. The subtleties of magma chamber partial crystallization processes can produce an astounding array of "pseudospidergrams," a small selection of which have been explored here. Major modification of the trace element geochemistry and trace element ratios, even those of the highly incompatible elements, must always be entertained whenever the evidence suggests the possibility of partial crystallization. At one extreme, periodically recharged, periodically tapped magma chambers might undergo partial crystallization by ˜95% consolidation of a succession of small packets of the magma. Refluxing of the 5% residual melts from such a process into the main body of melt would lead to eventual discrimination between highly incompatible elements in that residual liquid comparable with that otherwise achieved by 0.1 to 0.3% liquid extraction in equilibrium partial melting. Great caution needs to be exercised in attempting the reconstruction of more primitive compositions by addition of troctolite, gabbro, and olivine to apparently primitive lava compositions. Special attention is focussed on the phase equilibria involving olivine, plagioclase (i.e., troctolite), and liquid because a high proportion of erupted basalts carry these two phases as phenocrysts, yet the equilibria are restricted to crustal pressures and are only encountered by wide ranges of basaltic compositions at pressures less than 0.5 GPa. The mere presence of plagioclase phenocrysts may be sufficient to disqualify candidate primitive magmas. Determination of the actual contributions of crustal processes to petrogenesis requires a return to detailed field, experimental, and forensic petrologic studies of individual erupted basalt flows; of a multitude of cumulate gabbros and their contacts; and of upper-mantle outcrops.

Remarkable isotopic and trace element trends in potassic through sodic Cretaceous plutons of the Yukon-Koyukuk Basin, Alaska, and the nature of the lithosphere beneath the Koyukuk terrane

USGS Publications Warehouse

Arth, Joseph G.; Criss, Robert E.; Zmuda, Clara C.; Foley, Nora K.; Patton, W.W.; Miller, T.P.

1989-01-01

During the period from 110 to 80 m.y. ago, a 450-km-long magmatic belt was active along the northern margin of Yukon-Koyukuk basin and on eastern Seward Peninsula. The plutons intruded Upper Jurassic(?) and Lower Cretaceous volcanic arc rocks and Cretaceous sedimentary rocks in Yukon-Koyukuk basin and Proterozoic and lower Paleozoic continental rocks in Seward Peninsula. Within Yukon-Koyukuk basin, the plutons vary in composition from calc-alkalic plutons on the east to potassic and ultrapotassic alkalic plutons on the west. Plutons within Yukon-Koyukuk basin were analyzed for trace element and isotopic compositions in order to discern their origin and the nature of the underling lithosphere. Farthest to the east, the calc-alkalic rocks of Indian Mountain pluton are largely tonalite and sodic granodiorite, and have low Rb (average 82 ppm), high Sr (>600 ppm), high chondrite-normalized (cn) Ce/Yb (16–37), low δ18O (+6.5 to +7.1), low initial 87Sr/86Sr (SIR) (0.704), and high initial 143Nd/144Nd (NIR) (0.5126). These rocks resemble those modelled elsewhere as partial melts and subsequent fractionates of basaltic or gabbroic metaigneous rocks, and may be products of melting in the deeper parts of the Late Jurassic(?) and Early Cretaceous volcanic arc. Farthest to the west, the two ultrapotassic bodies of Selawik and Inland Lake are high in Cs (up to 93 ppm), Rb (up to 997 ppm), Sr, Ba, Th, and light rare earth elements, have high (Ce/Yb)cn (30, 27), moderate to low δ18O (+8.4, +6.9), high SIR (0.712, 0.710), and moderate NIR (0.5121–0.5122). These rocks resemble rocks of Australia and elsewhere that were modelled as melts of continental mantle that had been previously enriched in large cations. This mantle may be Paleozoic or older. The farthest west alkalic pluton of Selawik Hills is largely monzonite, quartz monzonite, and granite; has moderate Rb (average 284 ppm), high Sr (>600 ppm), high (Ce/Yb)cn (15–25), moderate δ18O (+8.3 to +8.6), high SIR (0.708–0.712), and moderate NIR (0.5121–0.5122). These rocks may be the product of interaction of magma derived from old continental mantle and magma derived from old continental crust. Plutons between eastern and western extremes show completely gradational variations in the concentration of K and Rb and in the isotopic compositions of Sr, Nd, and O. These plutons probably originated either by melting in a mixed source composed of a Paleozoic or older continental section (mantle + crust) overlain by Mesozoic mafic arc rocks, or by mixing of ultrapotassic to potassic magmas from continental sources (mantle + crust), and tonalitic magmas from arc sources. We infer from these results that the northwest portion of Yukon-Koyukuk basin is underlain by a substantial continental basement of Paleozoic or greater age. This basement probably thins out to the east. There is no geochemical evidence for continental basement east of about longitude 157°, or along a belt of at least 50 km width flanking Ruby Geanticline as far to the southwest as about longitude 161°. These areas are probably underlain by oceanic and Mesozoic arc rocks.

Drastic shift of lava geochemistry between pre- and post- Japan Sea opening in NE Japan subduction zone: constraints on source composition and slab surface melting processes

NASA Astrophysics Data System (ADS)

Okamura, S.; Inaba, M.; Igarashi, S.; Aizawa, M.; Shinjo, R.

2017-12-01

Isotopic and trace element data imply a temporal change in magma sources and thermal conditions beneath the northern Fossa Magna, NE Japan arc from the Oligocene to the Pleistocene. Less radiogenic 176Hf/177Hf and 143Nd/144Nd, and high Zr/Hf characterize the Oligocene - Early Miocene volcanism in the northern Fossa Magna region. The mantle wedge in the Oligocene - 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 Oligocene - 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. The Middle Miocene lavas characterized by most radiogenic Hf and Nd isotope ratios, have high Zr/Hf. 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 - Pleistocene samples are characterized by distinctly more radiogenic 176Hf/177Hf and 143Nd/144Nd, and are displaced toward lower Zr/Hf, which requires mixing between depleted mantle and a partial melt of subducted metasediment saturated with trace quantity of zircon. The Oligocene - Early Miocene volcanism in the northern Fossa Magna region may represent the early stage of continental margin magmatism associated with a back-arc rift. Here volcanism is dominated by sediment melts. Perhaps asthenospheric injection, triggering Japan Sea opening, allowed higher temperatures and more melting at the slab-mantle interface. The mantle wedge was gradually cooled during the Middle Miocene to the Pleistocene with back-arc opening ending in the Late Miocene. Slab surface temperatures were still high enough for sediments to melt but not too high (< 780 °C) to lose zircon as a residual phase.

Mantle heterogeneity in the source region of mid-ocean ridge basalts along the northern Central Indian Ridge (8°S-17°S)

NASA Astrophysics Data System (ADS)

Kim, Jonguk; Pak, Sang-Joon; Moon, Jai-Woon; Lee, Sang-Mook; Oh, Jihye; Stuart, Finlay M.

2017-04-01

The northern Central Indian Ridge (CIR) between 8°S and 17°S is composed of seven segments whose spreading rates increase southward from ˜35 to ˜40 mm/yr. During expeditions of R/V Onnuri to study hydrothermal activity on the northern CIR in 2009-2011, high-resolution multibeam mapping was conducted and ridge axis basalts were dredged. The major and trace element and Sr-Nd-Pb-He isotopic compositions of basaltic glasses dredged from the spreading axis require three mantle sources: depleted mantle and two distinct enriched mantle sources. The southern segments have Sr, Nd, and Pb that are a mix of depleted mantle and an enriched component as recorded in southern CIR MORB. This enrichment is indistinguishable from Rèunion plume mantle, except for He isotopes. This suggests that the southern segments have incorporated a contribution of the fossil Rèunion plume mantle, as the CIR migrated over hot-spot-modified mantle. The low 3He/4He (7.5-9.2 RA) of this enriched component may result from radiogenic 4He ingrowth in the fossil Rèunion mantle component. Basalts from the northern segments have high 206Pb/204Pb (18.53-19.15) and low 87Sr/86Sr (0.70286-0.70296) that are distinct from the Rèunion plume but consistent with derivation from mantle with FOZO signature, albeit with 3He/4He (9.2-11.8 RA) that are higher than typical. The FOZO-like enriched mantle cannot be attributed to the track of a nearby mantle plume. Instead, this enrichment may have resulted from recycling oceanic crust, possibly accompanied by small plume activity.

Timing of pyroxenite formation in supra-subduction Josephine Ophiolite, Oregon.

NASA Astrophysics Data System (ADS)

Hough, T.; Le Roux, V.; Kurz, M. D.

2017-12-01

The Josephine ophiolite is a partly dismembered ophiolite located in southern Oregon and northwestern California (USA). It displays a large ( 640 km2) mantle section that is mostly composed of depleted spinel harzburgite and lherzolite re-equilibrated at temperatures of 900 °C. In addition, the peridotite section of the ophiolite contains minor dunites and pyroxenite veins ranging from orthopyroxenites to clinopyroxenites. Using field, petrological and geochemical data, previous studies have shown that the peridotite experienced 10-20% of hydrous flux melting. In addition, clinopyroxene and orthopyroxene in harzburgites show variable degrees of light rare-earth element (LREE) enrichment, which suggests percolation and re-equilibration with small fractions of boninite melt. Overall, the trace element concentrations of pyroxenes indicate that the harzburgites experienced particularly high degrees of melting in the mantle wedge. We collected a number of orthopyroxenite and clinopyroxenite veins in the mantle section of the Josephine Ophiolite. Here we present the major and rare-earth element (REE) contents of pyroxene in 4 orthopyroxenites and 2 clinopyroxenites and calculate the major element and REE closure temperatures for individual veins. We show that individual pyroxenites record drastic variations in their degree of REE depletion, indicating that multiple generations of melts percolated the peridotite. The pyroxenite veins also record higher REE closure temperatures (>1200 ºC) compared to the surrounding peridotite, potentially indicating rapid cooling after emplacement. REE closure temperatures are also higher than major element closure temperatures. In parallel, we analyzed Sr isotopes by MC-ICPMS in pyroxene separates from 4 veins. Results indicate that the maximum age of emplacement of orthopyroxenite veins corresponds to the age of exhumation. Some clinopyroxenites may have formed during earlier melt percolation events. This study supports the idea that the composition of melts that percolate the mantle wedge can be highly variable and that orthopyroxenites may be the last type of veins to form in those environments.

Magma Chamber of the 26.5 ka Oruanui Eruption, Taupo Volcano, New Zealand

NASA Astrophysics Data System (ADS)

Liu, Y.; Anderson, A. T.; Wilson, C. J.; Davis, A. M.

2004-12-01

We have investigated melt inclusions and their host quartz crystals from the Bishop-Tuff-sized 26.5 ka Oruanui eruption at Taupo volcano, New Zealand. Compositions (major and trace elements, H2O and CO2) of melt inclusions and cathodoluminescence (CL) images of quartz were obtained for eight individual pumices from early, middle and late depositional units. All melt inclusions are high-silica weakly peraluminous rhyolites. Melt inclusions for different eruptive phases have similar ranges of H2O contents (3.8-5.2 wt %), but late-erupted samples have higher CO2 contents (mostly > 140 ppm). A positive correlation between CO2 and compatible trace elements such as Sr suggests that crystallization and melt entrapment occurred under gas-saturated conditions. Trace elements variations in melt inclusions are consistent with fractionation of 30-40 wt % crystals (plagioclase+quartz+pyroxene+amphibole). Crystal contents in pumices, trace-element contents in melt inclusions, and CL zoning patterns of quartz show no correlation with eruptive phases, suggesting that the Oruanui magma was well mixed before eruption. Some Oruanui quartz crystals contain distinctive CL zonings with a jagged ('restitic') core mantled by a black CL zone. Trace element variations in melt inclusions in the 'restitic' cores are consistent with fractionation of Ba-bearing minerals such as sanidine and/or biotite, both of which are rare or absent in rocks erupted from Taupo volcanic center. The above evidence suggests that Oruanui rhyolite is generated by assimilation of previous intruded rocks or country rocks, differentiated by crystal fractionation, and then mixed prior to eruption. Despite the differences in trace element and volatile contents, and crystal assemblages, both Bishop Tuff and Oruanui magmas involve crystal fractionation as one of the main differentiation mechanisms during their evolution. However, there are pronounced differences in the pre-eruptive stratification of the two chambers, which may reflect the tectonic settings, eruption rates, and ages of the systems.

High porosity harzburgite and dunite channels for the transport of compositionally heterogeneous melts in the mantle: II. Geochemical consequences

NASA Astrophysics Data System (ADS)

Liang, Y.; Schiemenz, A.; Xia, Y.; Parmentier, E.

2009-12-01

In a companion numerical study [1], we explored the spatial distribution of high porosity harzburgite and dunite channels produced by reactive dissolution of orthopyroxene (opx) in an upwelling mantle column and identified a number of new features. In this study, we examine the geochemical consequences of channelized melt flow under the settings outlined in [1] with special attention to the transport of compositionally heterogeneous melts and their interactions with the surrounding peridotite matrix during melt migration in the mantle. Time-dependent transport equations for a trace element in the interstitial melt and solids that include advection, dispersion, and melt-rock reaction were solved in a 2-D upwelling column using the high-order numerical methods outlined in [1]. The melt and solid velocities were taken from the steady state or quasi-steady state solutions of [1]. In terms of trace element fractionation, the simulation domain can be divided into 4 distinct regions: (a) high porosity harzburgite channel, overlain by; (b) high porosity dunite channel; (c) low porosity compacting boundary layer surrounding the melt channels; and (d) inter-channel regions outside (c). In the limit of local chemical equilibrium, melting in region (d) is equivalent to batch melting, whereas melting and melt extraction in (c) is more close to fractional melting with the melt suction rate first increase from the bottom of the melting column to a maximum near the bottom of the dunite channel and then decrease upward in the compacting boundary layer. The melt composition in the high porosity harzburgite channel is similar to that produced by high-degree batch melting (up to opx exhaustion), whereas the melt composition in the dunite is a weighted average of the ultra-depleted melt from the harzburgite channel below, the expelled melt from the compacting boundary layer, and melt produced by opx dissolution along the sidewalls of the dunite channel. Compaction within the dunite channel drives part of the channel melt in the upper part of the dunite channel into the surrounding harzburgite, providing a physical mechanism for shallow level re-fertilization or mantle metasomatism. The presence of compacting waves in and around a dunite-harzburgite channel system further complicates the melt flow field and provides new mechanisms for melt-peridotite interaction in the mantle. In the presence of chemical heterogeneity, the assumption of local equilibrium between the melt and its surrounding crystals results in significant chromatographic fractionation for incompatible trace elements in the melt percolating in region (d), and moderate fractionation for melt flowing through the harzburgite channel. Chemical disequilibrium between the melt and crystals reduces the extent of chromatographic fractionation during melt percolation and may be needed to explain the observed geochemical data. Alternatively, compositionally heterogeneous melts may be extracted through the high porosity melt channels without interaction with the peridotite matrix. [1] Schiemenz et al. submitted to AGU Fall meeting, 2009.

Petrology and geochemistry of primary magmas trapped in melt inclusions in scoria of Beaunit Maar (Chaîne des Puys, Massif Central, France)

NASA Astrophysics Data System (ADS)

Jannot, S.; Schiano, P.; Boivin, P.; Clocchiatti, R.; Chazot, G.

2003-04-01

The Massif Central area, characterized by a typical intraplate alkaline serie, is the largest magmatic province of the West-European Rift system. Although it has been the subject of several studies, the nature of Massif Central sources is still a matter of debate and many hypotheses are proposed, including deep-rooted continental hotspot, metasomatised spinel lherzolites and an asthenospheric flow linked to the lithospheric root of the Alpine chain. The Chaîne des Puys is the last magmatic province of the French Massif Central and is composed of hundred young well-preserved volcanoes. The present work aims to supply information on the nature and the origin of the source chemistry of alkaline serie from the Chaîne des Puys, by characterizing the trace and major element composition of minute melts preserved as quenched glass inclusions inside olivines phenocrysts in scoria from the Beaunit Maar. Heating stage experiments performed at ambient pressure on partially crystallised primary melt inclusions suggest CO_2 oversaturation of the trapped melt, and an entrapment temperature around 1200^oC±10^oC. Daughter minerals analyses point to a Ti-and Ca-rich basaltic paragenesis, in good agreement with that of erupted basalts from the Chaîne des Puys. Major element compositions show that melts trapped in inclusions evolve by limited fractional crystallization. Inclusions trapped in the more primitive olivine phenocrysts (Fo85) have alkali-basalt compositions that fall on the primitive end of the compositional trend define by the lavas of the Chaîne des Puys. Their major element chemistry rules out the hypothesis of a mantle source in the spinel stability field and requires a garnet-bearing mantle source. Analyzed for trace-element composition by LA-ICP-MS, they display homogeneous, enriched patterns, similar to those characterizing oceanic island and continental basalts. They have high concentration of LILE and LREE/HREE ratios. Such trace-element feature are typical of OIB showing EM(1-2)-type isotopic signatures and thought to reflect the involvement of recycled continental and/or sedimentary components.

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.

Plume-related mantle source of super-large rare metal deposits from the Lovozero and Khibina massifs on the Kola Peninsula, Eastern part of Baltic Shield: Sr, Nd and Hf isotope systematics

NASA Astrophysics Data System (ADS)

Kogarko, L. N.; Lahaye, Y.; Brey, G. P.

2010-03-01

The two world’s largest complexes of highly alkaline nepheline syenites and related rare metal loparite and eudialyte deposits, the Khibina and Lovozero massifs, occur in the central part of the Kola Peninsula. We measured for the first time in situ the trace element concentrations and the Sr, Nd and Hf isotope ratios by LA-ICP-MS (laser ablation inductively coupled plasma mass spectrometer) in loparite, eudialyte an in some other pegmatitic minerals. The results are in aggreement with the whole rock Sr and Nd isotope which suggests the formation of these superlarge rare metal deposits in a magmatic closed system. The initial Hf, Sr, Nd isotope ratios are similar to the isotopic signatures of OIB indicating depleted mantle as a source. This leads to the suggestion that the origin of these gigantic alkaline intrusions is connected to a deep seated mantle source—possibly to a lower mantle plume. The required combination of a depleted mantle and high rare metal enrichment in the source can be explained by the input of incompatible elements by metasomatising melts/fluids into the zones of alkaline magma generation shortly before the partial melting event (to avoid ingrowth of radiogenic isotopes). The minerals belovite and pyrochlore from the pegmatites are abnormally high in 87Sr /86Sr ratios. This may be explained by closed system isotope evolution as a result of a significant increase in Rb/Sr during the evolution of the peralkaline magma.

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.

Low helium flux from the mantle inferred from simulations of oceanic helium isotope data

NASA Astrophysics Data System (ADS)

Bianchi, Daniele; Sarmiento, Jorge L.; Gnanadesikan, Anand; Key, Robert M.; Schlosser, Peter; Newton, Robert

2010-09-01

The high 3He/ 4He isotopic ratio of oceanic helium relative to the atmosphere has long been recognized as the signature of mantle 3He outgassing from the Earth's interior. The outgassing flux of helium is frequently used to normalize estimates of chemical fluxes of elements from the solid Earth, and provides a strong constraint to models of mantle degassing. Here we use a suite of ocean general circulation models and helium isotope data obtained by the World Ocean Circulation Experiment to constrain the flux of helium from the mantle to the oceans. Our results suggest that the currently accepted flux is overestimated by a factor of 2. We show that a flux of 527 ± 102 mol year - 1 is required for ocean general circulation models that produce distributions of ocean ventilation tracers such as radiocarbon and chlorofluorocarbons that match observations. This new estimate calls for a reevaluation of the degassing fluxes of elements that are currently tied to the helium fluxes, including noble gases and carbon dioxide.

Trace element analysis by PIXE in several biomedical fields

NASA Astrophysics Data System (ADS)

Weber, G.; Robaye, G.; Bartsch, P.; Collignon, A.; Beguin, Y.; Roelandts, I.; Delbrouck, J. M.

1984-04-01

Since 1980 in the University of Liége trace element analysis by PIXE has been developed in several directions, among these: the elemental composition of lung parenchyma, hilar lymph nodes, blood content in hematological disorders and renal insufficiency. The content in trace elements of lung tumor and surrounding tissue is measured and compared to similar content previously obtained on unselected patients of comparable ages. The normalization of the bromine deficiency observed in hemodialized patients is achieved by using a dialyzing bath doped with NaBr in order to obtain a normal bromine level of 5.7 μg/ml. The content of Cu, Zn, Br and Se in blood serum from more than 100 patients suffering from malignant hemopathy has been measured. The results are compared with a reference group. These oligoelements have also been measured sequentially for patients under intensive chemotherapy in acute myeloid leukemia.

Trace element contamination in feather and tissue samples from Anna’s hummingbirds

USGS Publications Warehouse

Mikoni, Nicole A.; Poppenga, Robert H.; Ackerman, Joshua T.; Foley, Janet E.; Hazlehurst, Jenny; Purdin, Güthrum; Aston, Linda; Hargrave, Sabine; Jelks, Karen; Tell, Lisa A.

2017-01-01

Trace element contamination (17 elements; Be, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Ba, Hg, Tl, and Pb) of live (feather samples only) and deceased (feather and tissue samples) Anna's hummingbirds (Calypte anna) was evaluated. Samples were analyzed using inductively coupled plasma-mass spectrometry (ICP-MS; 17 elements) and atomic absorption spectrophotometry (Hg only). Mean plus one standard deviation (SD) was considered the benchmark, and concentrations above the mean + 1 SD were considered elevated above normal. Contour feathers were sampled from live birds of varying age, sex, and California locations. In order to reduce thermal impacts, minimal feathers were taken from live birds, therefore a novel method was developed for preparation of low mass feather samples for ICP-MS analysis. The study found that the novel feather preparation method enabled small mass feather samples to be analyzed for trace elements using ICP-MS. For feather samples from live birds, all trace elements, with the exception of beryllium, had concentrations above the mean + 1 SD. Important risk factors for elevated trace element concentrations in feathers of live birds were age for iron, zinc, and arsenic, and location for iron, manganese, zinc, and selenium. For samples from deceased birds, ICP-MS results from body and tail feathers were correlated for Fe, Zn, and Pb, and feather concentrations were correlated with renal (Fe, Zn, Pb) or hepatic (Hg) tissue concentrations. Results for AA spectrophotometry analyzed samples from deceased birds further supported the ICP-MS findings where a strong correlation between mercury concentrations in feather and tissue (pectoral muscle) samples was found. These study results support that sampling feathers from live free-ranging hummingbirds might be a useful, non-lethal sampling method for evaluating trace element exposure and provides a sampling alternative since their small body size limits traditional sampling of blood and tissues. The results from this study provide a benchmark for the distribution of trace element concentrations in feather and tissue samples from hummingbirds and suggests a reference mark for exceeding normal. Lastly, pollinating avian species are minimally represented in the literature as bioindicators for environmental trace element contamination. Given that trace elements can move through food chains by a variety of routes, our study indicates that hummingbirds are possible bioindicators of environmental trace element contamination.

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.

Geochemical models of melting and magma storage conditions for basalt lava from Santorini Volcano, Greece

NASA Astrophysics Data System (ADS)

Baziotis, Ioannis; Kimura, Jun-Ichi; Pantazidis, Avgoustinos; Klemme, Stephan; Berndt, Jasper; Asimow, Paul

2017-04-01

Santorini volcano sits ˜150 km above the Wadati-Benioff zone of the Aegean arc, where the African plate subducts northward beneath the Eurasian continent (Papazachos et al. 2000). Santorini volcano has a long history: activity started ca. 650 ka (mainly rhyolites and rhyodacites), with active pulses following ca. 550 ka (basalt to rhyodacite) and ca. 360 ka (large explosive eruptions of andesite to rhyodacite and minor basalt), culminating in the caldera-forming Bronze-age Minoan event (Druitt et al. 1999). As in many arc volcanoes, scenarios of fractional crystallization with or without mixing between felsic and mafic magmas have been proposed to explain the compositions, textures, and eruptive styles of Santorini products (e.g., Huijsmans & Barton 1989; Montazavi & Sparks 2004; Andújar et al. 2015). Here we focus on a basalt lava from the southern part of Santorini volcano (Balos cove, 36˚ 21.7'N, 25˚ 23.8'E), one of the few basaltic localities in the Aegean arc. The goals are to infer constraints on the magma chamber conditions which lead to mafic eruption at Santorini Volcano and to evaluate the slab and mantle wedge conditions via geochemical and petrological mass balance modelling. We collected and characterised 20 samples for texture (SEM), mineral chemistry (FE-EPMA) and whole-rock chemistry (XRF). The basalts contain phenocrystic olivine (Ol) and clinopyroxene (Cpx) (<600 μm diameter) in a fine groundmass (<100 μm diameter) of Ol, Cpx, plagioclase (Pl) and magnetite (Mt) with minor glass and rare xenocrystic quartz. Santorini basalts exhibit a pilotaxitic to trachytic texture defined by randomly to flow-oriented tabular Pl, respectively. The predominant minerals are calcic Pl (core An78-85 and rim An60-76; 45-50 vol.%), Cpx (En36-48Wo41-44Fs11-21; 10-15 vol.%) and Ol (Fo74-88; 10-12 vol.%). Idiomorphic to subidiomorphic Mt (<10μm diameter) with variable TiO2 contents (1.9-16.5 wt%) is a minor constituent (˜1-2 vol.%) in the less mafic samples. Observed mineralogy and major element chemistry suggest fractionation in a shallow magma chamber. Using the major element chemistry and PRIMACALC2 (Kimura & Ariskin 2014) back-calculator, inferred crystallization conditions are P=0.02 GPa, oxidized (fO2=QFM+2), and ˜1 wt% H2O in the primary basalt. The source mantle conditions are estimated at P=2.1 GPa, T=1350˚ C, and degree of melting F=8%. We also used trace elements to estimate the incompatible element budget of the primary basalt using the forward trace-element mass-balance model of ARC BASALT SIMULATOR ver.4 (Kimura et al. 2014). Preliminary results suggest that the slab flux was derived from ˜150 km depth, and fluxed mantle melting occurred at P=2.3 GPa, T=1380˚ C, F=8%. The estimated slab depth is consistent with the seismic observations and mantle conditions are consistent with the PRIMACALC2 major element modelling. Our intent is to extend our analytical data with precise trace element and isotope analyses in order to reveal more detailed source conditions and richer information about processes from the slab through the mantle and up to the shallow magma chamber. References Andújar, J. et al. (2015). JPET, 56 (4), 765-794. Druitt, et al. (1999). Geological Society Memoir, 19. Huijsmans, J. P., & Barton, M. (1989). JPET, 30(3), 583-625. Kimura, J. I., & Ariskin, A. A. (2014). G3, 15, 1494-1514. Kimura, J. I. et al. (2014). G3, 15, 691-739. Mortazavi, M., & Sparks, R. S. J. (2004). Con Min Pet, 146(4), 397-413. Papazachos, et al. (2000). Tectonophysics, 319(4), 275-300.

The role of high-energy synchrotron radiation in biomedical trace element research

DOE Office of Scientific and Technical Information (OSTI.GOV)

Pounds, J.G.; Long, G.J.; Kwiatek, W.M.

1987-01-01

This paper will present the results of an investigation of the distribution of essential elements in the normal hepatic lobule. the liver is the organ responsible for metabolism and storage of most trace elements. Although parenchymal hepatocytes are rather uniform histologically, morphometry, histochemistry, immunohistochemistry, and microdissection with microchemical investigations have revealed marked heterogeneity on a functional and biochemical level. Hepatocytes from the periportal and perivenous zones of the liver parrenchyma differ in oxidative energy metabolism, glucose uptake and output, unreagenesis, biotransformation, bile acid secretion, and palsma protein synthesis and secretion. Although trace elements are intimately involved in the regulation andmore » maintenance of these functions, little is known regarding the heterogeneity of trace element localization of the liver parenchyma. Histochemical techniques for trace elements generally give high spatial resolution, but lack specificity and stoichiometry. Microdissection has been of marginal usefulness for trace element analyses due to the very small size of the dissected parenchyma. The characteristics of the high-energy x-ray microscope provide an effective approach for elucidating the trace element content of these small biological structures or regions. 5 refs., 1 fig., 1 tab.« less

Origin and geodynamic setting of Late Cenozoic granitoids in Sulawesi, Indonesia

NASA Astrophysics Data System (ADS)

Maulana, Adi; Imai, Akira; Van Leeuwen, Theo; Watanabe, Koichiro; Yonezu, Kotaro; Nakano, Takanori; Boyce, Adrian; Page, Laurence; Schersten, Anders

2016-07-01

Late Cenozoic granitoids are widespread in a 1600 km long belt forming the Western and Northern Sulawesi tectono-magmatic provinces. They can be divided into three rock series: shoshonitic (HK), high-K felsic calc-alkaline (CAK), and normal calc-alkaline to tholeiitic (CA-TH). Representative samples collected from eleven plutons, which were subjected to petrography, major element, trace element, Sr, Nd, Pb isotope and whole-rock δ18O analyses, are all I-type and metaluminous to weakly peraluminous. The occurrence of the two K-rich series is restricted to Western Sulawesi, where they formed in an extensional, post-subduction tectonic setting with astenospheric upwelling providing thermal perturbation and adiabatic decompression. Two parental magma sources are proposed: enriched mantle or lower crustal equivalent for HK magmas, and Triassic igneous rocks in a Gondwana-derived fragment thrust beneath the cental and northern parts of Western Sulawesi for CAK magmas. The latter interpretation is based on striking similarities in radiogenic isotope and trace element signatures. CA-TH granitoids are found mostly in Northern Sulawesi. Partial melting of lower-middle crust amphibolites in an active subduction environment is the proposed origin of these rocks. Fractional crystallization and crustal contamination have played a significant role in magma petrogenesis, particularly in the case of the HK and CAK series. Contamination by organic carbon-bearing sedimentary rocks of the HK and CAK granitoids in the central part of Western Sulawesi is suggested by their ilmenite-series (reduced) character. The CAK granitoids further to the north and CA-TH granitoids in Northern Sulawesi are typical magnetite-series (oxidized). This may explain differences in mineralization styles in the two regions.

Oxygen isotopes and volatile contents of the Gorgona komatiites, Colombia: A confirmation of the deep mantle origin of H2O

NASA Astrophysics Data System (ADS)

Gurenko, Andrey A.; Kamenetsky, Vadim S.; Kerr, Andrew C.

2016-11-01

We report O isotopes in olivine grains (Fo89-93) and volatile contents (CO2, H2O, F, S, Cl) in olivine-hosted melt inclusions from one Gorgona picrite and five komatiites with the aim of constraining the origin of H2O in these magmas. These samples have previously been analysed for major and trace elements and volatile concentrations (H2O, S, Cl) and B isotopes in melt inclusions. A distinctive feature of the included melts is relatively high contents of volatile components and boron, which show positive anomalies in, otherwise depleted, primitive mantle normalised trace and rare earth element patterns and range in δ11 B from -11.5 to 15.6‰. In this study, the olivines were systematically analysed for O isotopes (1) in the centre of grains, (2) near the grain boundaries and, (3) as close as possible to the studied melt inclusions. The majority of olivines (∼66%) are ;mantle;-like, 4.8 ‰ ≤δ18 O ≤ 5.5 ‰, with a subordinate but still significant number (∼33%) above, and only 2 grains below, this range. There is no systematic difference between the central and marginal parts of the grains. Higher than ;mantle; δ18OOl values are ascribed to low-T (<300 °C) serpentinisation along inner fractures and grain boundaries of olivine phenocrysts. The measured concentrations of volatile components in the melt inclusions corrected for the effects of post-entrapment crystallisation and H2O-CO2 exsolution in inclusion shrinkage bubbles are: 286-1748 μg/g CO2, 0.2-0.86 wt.% H2O, 48-82 μg/g F, 398-699 μg/g S and 132-198 μg/g Cl. They correspond to a pressure of 86 ± 44MPa or ∼2.5-km crustal depth of olivine crystallisation. The correlations of S and, to a lesser extent, of H2O, with highly incompatible lithophile elements and the correlation of F with Cl, but no relationships of H2O with Cl, rule out shallow depth magma degassing and/or crustal contamination. Our new δ18 O olivine and volatile component data combined with the existing, highly variable δ11 B values for melt inclusions also support the deep mantle origin of H2O (and probably other volatiles) in the Gorgona mafic and ultramafic magmas.

The Role of Hydrous Slab Melts in the Sulfur Content, Metal Content, and Oxidation State of Primitive Arc Magmas in the Southern Cascades

NASA Astrophysics Data System (ADS)

Muth, M.; Wallace, P. J.; Walowski, K. J.

2017-12-01

Arc magmas have an oxidized signature (higher Fe3+/∑Fe) relative to MORB. This oxidized signature could be developed during crustal differentiation or be derived from slab components such as hydrous melts and ­fluids. Previous work in the Lassen region of the Cascade arc shows evidence for the addition of a hydrous slab component to the mantle wedge beneath the southern Cascades [1]. Here we investigate whether this hydrous slab component is linked to the oxidation state of primitive magmas using the sulfur, metal, and trace element concentrations of olivine-hosted melt inclusions. Melt inclusions were selected from the tephra of three cinder cones in Lassen volcanic field and analyzed for trace elements and metals (Cu, Zn, Sn) using LA-ICPMS and for major elements, S, and Cl using EMPA. Sulfur concentrations in individual melt inclusions range from 900 to 2200 ppm. Cu, Zn, and Sn concentrations in individual melt inclusions range from 17 to 167 ppm, 65 to 127 ppm, and 0.4 to 1.4 ppm, respectively. Average sulfur concentrations are different for each of the three cinder cones, and individual melt inclusion S/Dy values correlate well with Sr/Nd values. This is an indication that, like other volatiles, sulfur is supplied to the mantle wedge by a slab-derived component. To assess whether this sulfur-carrying slab component affects the oxidation state of the mantle wedge during melting, we used estimates of sulfur content at sulfide saturation to place a minimum bound on fO2 values for the primitive magmas at each cinder cone. These values range from QFM to QFM + 1.5. Despite this wide range of fO2 values, the concentrations of Cu and other metals are low relative to values predicted by partial melting of the mantle wedge during relatively oxidized (greater than QFM + 1.3) conditions [2], and do not vary systematically with indicators of slab component addition such as Sr/Nd. This suggests that metals are not derived from the slab component and/or that residual sulfide is present during melting across the wide range of fO2 values. This observation is also consistent with the addition of a sulfur-carrying slab component to the mantle wedge. Future work will compare these observations to direct measurement of Fe3+/∑Fe and S6+/∑S using XANES. [1] Walowski et al. 2016, EPSL. [2] Lee et al. 2012, Science.

A Crystal Stratigraphy Approach to Deciphering the Petrogenesis of the Detroit Seamount

NASA Astrophysics Data System (ADS)

Simonetti, A.; Davenport, J.; Neal, C. R.

2012-12-01

The Detroit Seamount (DSM) erupted ~76-81 Ma ago, and is the northwestern terminus of the Hawaiian-Emperor Seamount chain. The Hawaiian-Emperor Seamount chain has drastically furthered our understanding of how and where mantle plumes originate, the dynamics of interactions between plumes and mantle, and plate movement in the recent past. DSM Basalts from Site 1203 of Leg 197 of the Ocean Drilling Program (ODP) contain, by rock volume, a large quantity of plagioclase and olivine phenocrysts. Previous investigations into magma chamber processes via phenocryst analysis such as those occurring at the DSM have largely relied solely on major and trace element analyses. However, since both are easily susceptible to post-solidification alteration processes, in this study we are undertaking a multi-faceted approach to deciphering the petrogenetic history of the DSM basalts via crystal stratigraphy, crystal size distributions (CSDs), electron microprobe analysis (EPMA), laser ablation and multi-collector inductively coupled plasma mass spectrometry (LA- and MC-ICP-MS), microdilling and phase separation, and isotope analysis of whole-rock, olivine and plagioclase phenocrysts and their associated melt inclusions. A preliminary Sr isotope and trace element investigation of DSM whole rock basalts from Site 884 yielded a range of values between 0.70262 and 0.70276, as well as MORB-like trace element patterns. Notably, the plagioclase rims analyzed possessed a more radiogenic (87Sr/86Sr)I than the core (0.70361 ± 2 vs. 0.70347 ± 2). Our initial interpretation of this radiogenic increase from core-to-rim was crystal growth in an OIB-rich magma source that was not cogenetic with its matrix. Eight olivine phenocrysts from DSM basalts were analyzed for major elements using scanning electron microscopy (SEM) and energy dispersive spectrum (EDS) techniques. Fosterite contents of the olivine phenocrysts range from 84-86. Olivines from basalt sample 10R-4 exhibit a well-defined correlation between Ni and Mn contents, whereas those from sample 10R-3 show a more limited range of Mn and Ni compositions. The trends defined by the data from the olivine phenocrysts clearly suggest that fractional crystallization was not the sole magma differentiation process to have occurred. Rare earth element (REE) abundances for the olivine phenocrysts are low, and generally range from 0.1 to 2 ppm, with those from basalt sample 10R-4 containing higher abundances than sample 10R-3. Melt inclusions from within plagioclase phenocrysts in DSM basalt sample 9R-2 from Site 884 were analyzed via laser ablation-ICP-MS. Results from the analyses indicate that the melt inclusions are LREE-enriched and negatively-sloped compared to the LREE-depleted basalt whole rock compositions from the DSM and the East Pacific Rise. Of interest, the La concentrations in the melt inclusions are notably similar to abundances found for the Manua Kea tholeiites. Trace element data and Sr isotope ratios for both melt inclusions and phenocrysts from the DSM basalts are all indicative of open system behavior and possibly consistent with magma mixing between at least two end-member mantle components.

Petrology of basalts from Loihi Seamount, Hawaii

NASA Astrophysics Data System (ADS)

Hawkins, James; Melchior, John

1983-12-01

Loihi Seamount is the southeasternmost active volcano of the Emperor-Hawaii linear volcanic chain. It comprises a spectrum of basalt compositional varieties including basanite, alkali basalt, transitional basalt and tholeiite. Samples from four dredge collections made on Scripps Institution of Oceanography Benthic Expedition in October 1982 are tholeiite. The samples include highly vesicular, olivine-rich basalt and dense glass-rich pillow fragments containing olivine and augite phenocrysts. Both quartz-normative and olivine-normative tholeiites are present. Minor and trace element data indicate relatively high abundances of low partition coefficient elements (e.g., Ti, K, P. Rb, Ba, Zr) and suggest that the samples were derived by relatively small to moderate extent of partial melting, of an undepleted mantle source. Olivine composition, MgO, Cr and Ni abundances, and Mg/(Mg+Fe), are typical of moderately fractionated to relatively unfractionated "primary" magmas. The variations in chemistry between samples cannot be adequately explained by low-pressure fractional crystallization but can be satisfied by minor variations in extent of melting if a homogeneous source is postulated. Alternatively, a heterogeneous source with variable abundances of certain trace elements, or mixing of liquids, may have been involved. Data for 3He/ 4He, presented in a separate paper, implies a mantle plume origin for the helium composition of the Loihi samples. There is little variation in the helium isotope ratio for samples having different compositions and textures. The helium data are not distinctive enough to unequivocally separate the magma sources for the tholeiitic rocks from the other rock types such as Loihi alkalic basalts and the whole source region for Loihi may have a nearly uniform helium compositions even though other element abundances may be variable. Complex petrologic processes including variable melting, fractional crystallization and magma mixing may have blurred original helium isotopic signatures.

In-place alkalic lavas recovered from Hilina Bench off-shore Kilauea, Hawaii: significance in reconstructing ancient Kilauea history

NASA Astrophysics Data System (ADS)

Kimura, J.; Sisson, T. W.; Coombs, M.; Lipman, P. W.

2002-12-01

Lava samples recovered from off-shore Hawaii Island, using remote and manned submersibles during JAMSTEC cruises in 1998, 1999, and 2001, were analyzed for major and trace elements. On the scarp below the Hilina bench (~ 3000 m bmsl), clasts of alkali and transitional basalt were recovered from debris-flow breccias, but tholeiite basalt of modern Kilauea type is absent (Sisson et al., 2002). In 2001 (dive K508), a succession of in-place pillow lavas of alkali basalt was found for the first time on the slope above the Hilina bench, along a well-exposed a rib. These in-place samples of alklic material in relative shallow water depths provide a critical link between modern-day and ancestral Kilauea. The rib is part of ancient Kilauea volcano that has remained in place, while the Hilina Bench contains slide/slump material from Kilauea (Lipman et al., 2002). At the same water depths but ~15 km to the southwest, Dive K207 sampled a series of alkali basalt breccia clasts that are compositionally similar to the in-place lavas of K208. In contrast, a dive on Papa'u Seamount (K509), located at the upper southwest margin of the bench, traversed massive breccias of subaerially erupted tholeiitic basalt. The breccias are compositionally similar to Mauna Loa lavas, and must be ancient landslide material from this volcano. Geochemical characteristics of transitional basalts from the slope above the Hilina bench are related to historical Kilauea tholeiites in major and trace elements. Alkali basalts from both the lower flank of the Hilina bench and the upper rib are more Ti rich than the transitional basalts, with elevated light-rare-earth and large-ion-lithophile elements. Various binary plots between highly incompatible trace element pairs define confined straight lines, including historical Kilauea tholeiite, the transitional basalts, and the Hilina alkalic pillows, suggesting a common mantle source with different degrees of partial melting. However, chemistry of these basalts differ from the more alkalic basanite and nephelinite lava clasts from the lower flank (Sisson et al., 2002). The highly alkaline lavas would have derived from different mantle sources, perhaps from perimeters of the Hawaiian mantle plume, whereas alkali, transitional, and tholeiitic basalts are from more central parts of the plume. The in-place alkalic pillow basalts provides new insights on earlier growth history and changes in states of basalt sources during the magmatic evolution of Kilauea, which is still in progress.

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.

Early Terrestrial Mantle Differentiation Recorded in Paleoarchean Komatiites

NASA Astrophysics Data System (ADS)

Puchtel, I. S.; Blichert-Toft, J.; Touboul, M.; Horan, M. F.; Walker, R. J.

2016-12-01

Geochmical signatures generated in the manle as a result of radioactive decay of short- and long-lived nuclides can be used to constrain the timing of formation and the nature of now mostly vanished early terrestrial reservoirs. The 3.55 Ga komatiites from the Schapenburg Greenstone Remnant (SGR) located in the Barberton Greenstone Belt in South Africa have a unique combination of trace element abundances and isotopic compositions that place strong constraints on the origin of these reservoirs. The SGR komatiites define a Re-Os isochron with an age of 3550±87 Ma and an initial γ187Os = +3.7±0.2 (2SD). The absolute HSE abundances in the mantle source of the SGR komatiite system are estimated to be only 29±5% of those in the present-day bulk silicate Earth (BSE) estimates. The SGR komatiites show coupled depletion, relative to the modern mantle, in 142Nd and 182W (μ142Nd = -5.0±2.8, μ182W = -8.4±4.5), the decay products of the short-lived 146Sm and 182Hf nuclides, respectively, indicating derivation from a mantle domain that was enriched in incompatible elements 30 Ma after Solar System formation. Early Hadean contributors to this mantle domain could include high-pressure fractionates from a primordial magma ocean. By contrast, the long-lived Sm-Nd and Lu-Hf isotope systems (ɛ143Nd = +2.4±0.1, ɛ176Hf = +5.7±0.3) indicate that the mantle domain that the SGR komatiites were ultimately derived from underwent additional processing after the early Hadean, including melt depletion at lower pressures. The preservation of early-formed 182W and 142Nd anomalies in the mantle until at least 3.55 Ga indicates that the products of early planetary differentiation survived both later planetary accretion and convective mantle mixing during the Hadean. This study lends further support to the notion that variable late accretion, by itself, cannot account for all of the observed W isotope and absolute and relative HSE abundance variations in the Archean mantle recorded by komatiites.

The Whitish Inner Mantle of the Giant Clam, Tridacna squamosa, Expresses an Apical Plasma Membrane Ca2+-ATPase (PMCA) Which Displays Light-Dependent Gene and Protein Expressions

PubMed Central

Ip, Yuen K.; Hiong, Kum C.; Goh, Enan J. K.; Boo, Mel V.; Choo, Celine Y. L.; Ching, Biyun; Wong, Wai P.; Chew, Shit F.

2017-01-01

Giant clams live in symbiosis with extracellular zooxanthellae and display high rates of growth and shell formation (calcification) in light. Light-enhanced calcification requires an increase in the supply of Ca2+ to, and simultaneously an augmented removal of H+ from, the extrapallial fluid where shell formation occurs. We have obtained the complete coding cDNA sequence of Plasma Membrane Ca2+-ATPase (PMCA) from the thin and whitish inner mantle, which is in touch with the extrapallial fluid, of the giant clam Tridacna squamosa. The deduced PMCA sequence consisted of an apical targeting element. Immunofluorescence microscopy confirmed that PMCA had an apical localization in the shell-facing epithelium of the inner mantle, whereby it can actively secrete Ca2+ in exchange for H+. More importantly, the apical PMCA-immunofluorescence of the shell-facing epithelium of the inner mantle increased significantly after 12 h of exposure to light. The transcript and protein levels of PMCA/PMCA also increased significantly in the inner mantle after 6 or 12 h of light exposure. These results offer insights into a light-dependable mechanism of shell formation in T. squamosa and a novel explanation of light-enhanced calcification in general. As the inner mantle normally lacks light sensitive pigments, our results support a previous proposition that symbiotic zooxanthellae, particularly those in the colorful and extensible outer mantle, may act as light-sensing elements for the host clam. PMID:29066980

The Whitish Inner Mantle of the Giant Clam, Tridacna squamosa, Expresses an Apical Plasma Membrane Ca2+-ATPase (PMCA) Which Displays Light-Dependent Gene and Protein Expressions.

PubMed

Ip, Yuen K; Hiong, Kum C; Goh, Enan J K; Boo, Mel V; Choo, Celine Y L; Ching, Biyun; Wong, Wai P; Chew, Shit F

2017-01-01

Giant clams live in symbiosis with extracellular zooxanthellae and display high rates of growth and shell formation (calcification) in light. Light-enhanced calcification requires an increase in the supply of Ca 2+ to, and simultaneously an augmented removal of H + from, the extrapallial fluid where shell formation occurs. We have obtained the complete coding cDNA sequence of Plasma Membrane Ca 2+ -ATPase ( PMCA ) from the thin and whitish inner mantle, which is in touch with the extrapallial fluid, of the giant clam Tridacna squamosa . The deduced PMCA sequence consisted of an apical targeting element. Immunofluorescence microscopy confirmed that PMCA had an apical localization in the shell-facing epithelium of the inner mantle, whereby it can actively secrete Ca 2+ in exchange for H + . More importantly, the apical PMCA-immunofluorescence of the shell-facing epithelium of the inner mantle increased significantly after 12 h of exposure to light. The transcript and protein levels of PMCA /PMCA also increased significantly in the inner mantle after 6 or 12 h of light exposure. These results offer insights into a light-dependable mechanism of shell formation in T. squamosa and a novel explanation of light-enhanced calcification in general. As the inner mantle normally lacks light sensitive pigments, our results support a previous proposition that symbiotic zooxanthellae, particularly those in the colorful and extensible outer mantle, may act as light-sensing elements for the host clam.

Geochemistry of the Bela Ophiolite, Pakistan

NASA Astrophysics Data System (ADS)

Khan, M.; Nicholson, K. N.; Mahmood, K.

2008-12-01

The Bela ophiolite complex of Balochistan, Pakistan has been the subject of several geochemical and tectonic studies in the past. However until now there has never been a combined structural, geochemical and tectonic assimilation study which adequately explains the observed geochemistry and structural geology in a global tectonic framework. Here we present the geochemical findings of our work. The Bela ophiolite complex consists of two major units: the basal section or Lower Unit, and the Upper Unit, between the two is a mélange zone. The Lower Unit is relatively homogeneous and consists almost entirely of flow basalts and pillow basalts. The base of the Upper Unit is the metamorphic sole which is overlain by a sequence of massive basalts flows and intrusions of gabbro and granites. The entire Upper Unit is cut by doleritic dykes and sills. Geochemically the Lower Unit is comprised of basaltic lavas with E-MORB affinities. These lavas are tholeiitic, low-K series lavas with trace element signatures of E-type MORB. For example ratios such as V/Ti, Zr/Y, Nb/Th, Th/La and Nb/U all suggest these lavas are E-MORB. Previous workers have suggested these lavas are back-arc basin (BAB) however the samples lack the characteristic signatures of subduction modified MORB. This conclusion is supported by chondrite and N-MORB normalized spider diagrams where the Lower Unit lavas are enriched in the LILE with respect to the HFSE. The Upper Unit of the Bela Ophiolite sequence has a slightly more complex history. The older lavas sequences, the massive basalt flows, gabbros and granites, all formed in an oceanic arc environment. These lavas exhibit classic arc signatures such as a negative Nb and Ti anomalies, are enriched in LILE and LREE relative to HSFE, and plot in the volcanic arc and island arc fields in classic ternary plots such as 2Nb- Zr/4-Y and Y/15-La/10-Nb/8. The younger sequence of intrusions found in the Bela ophiolite appear to have BAB signatures. These lavas have relatively flat MORB normalized plots, are slightly depleted in the LILE relative the HFSE, and have a very small negative Nb anomaly. Source characteristics for both units have been determined using trace element data. This work suggests that the E-MORB lavas are derived from partial melting of enriched mantle. The lavas found in the Upper Unit have all been sourced from depleted or N-MORB mantle which has been modified by subducting fluids. It is possible that the younger BAB samples have a slightly more enriched source than the corresponding arc lavas which might indicate movement of the subduction zone allowing the influx of new mantle material below the wedge. In conclusion, our new geochemical work shows that the Bela ophiolite contains three distinct magmatic sequences: a lower E-MORB sequence over lain by a series of volcanic arc lavas which are cut by BAB-type sills and dykes.

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.

Trace-element concentrations in streambed sediment across the conterminous United States

USGS Publications Warehouse

Rice, Karen C.

1999-01-01

Trace-element concentrations in 541 streambed-sediment samples collected from 20 study areas across the conterminous United States were examined as part of the National Water-Quality Assessment Program of the U.S. Geological Survey. Sediment samples were sieved and the <63-μm fraction was retained for determination of total concentrations of trace elements. Aluminum, iron, titanium, and organic carbon were weakly or not at all correlated with the nine trace elements examined:  arsenic, cadmium, chromium, copper, lead, mercury, nickel, selenium, and zinc. Four different methods of accounting for background/baseline concentrations were examined; however, normalization was not required because field sieving removed most of the background differences between samples. The sum of concentrations of trace elements characteristic of urban settings - copper, mercury, lead, and zinc - was well correlated with population density, nationwide. Median concentrations of seven trace elements (all nine examined except arsenic and selenium) were enriched in samples collected from urban settings relative to agricultural or forested settings. Forty-nine percent of the sites sampled in urban settings had concentrations of one or more trace elements that exceeded levels at which adverse biological effects could occur in aquatic biota.

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.

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).

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.

The Debate on the Prospective Interaction between SWIR 46°-52°E and Crozet hotspot: Constrain from the Geochemical Characteristics and Helium isotopes of MORBs from Southwest Indian Ridge

NASA Astrophysics Data System (ADS)

Yu, X.; Dick, H. J. B.; Chu, F.; Li, X.; Tang, L.

2017-12-01

The Southwest Indian Ridge with obvious mantle heterogeneity is often attributed to the influence of nearby hotspots. The Dragon Flag Supersegment between 46°E and 52°E on Marion Rise has thicker crust, shallower axial depth, and lower mantle Bouguer anomaly, which indicates ridge-hotspot interaction. However, the great distance between Crozet hotspot and the supersegment (about 1,000km) and the controversial geochemical data are both against the prospective ridge-hotspot interaction. Here we compiled major element, trace element, Sr-Nd-Pb and He isotopic data of new samples from the supersegment. The mantle source, partial melting process as well as the crystallization history of these basalts are further constrained based on the synthetic analysis of the dataset. Most basalts from the supersegment require 0 to 30% olivine and plagioclase fractionation to account for their present composition, whereas the crystallization of clinopyroxene appears to be rather limited. The parental magmas of the supersegment are distinctive from east to west. Most samples from the Eastern Group can be modeled as the product of 10% partial melting of a DMM-like source, while some extremely depleted samples from the central valley may require two stages of partial melting, i.e. ancient melting of DMM-like source, followed by recent remelting of the residues. The Western Group may be resulted from lower degree of partial melting (5-10%), or a previously less depleted mantle source. The Eastern Group is favor of the involvement of Crozet hotspot in terms of Pb isotope and helium isotope signatures, but the trace element and Sr-Nd isotopes are not supportive for this interaction. The especially high 206Pb/204Pb for some of the samples from the Eastern Group, similar to the Crozet hotspot, requires the sporadical entrainment of blobs of relatively enriched source material, like the Crozet component. The Crozet hotspot is distinctive in its Sr-Nd-Pb-He isotopes among different islands, thus it is more complicate to address the issue of ridge-hotspot interaction. We suggest that the prospective Crozet-SWIR interaction is possible and can explain most of the geological and geochemical signatures.

The Ins and Outs of Water in the Earth's Mantle

NASA Astrophysics Data System (ADS)

Hauri, E. H.; Gaetani, G. A.; Shaw, A. M.; Kelley, K. A.; Saal, A. E.

2005-12-01

Most of the hydrogen in the Earth's upper mantle is dissolved in nominally anhydrous minerals such as olivine, orthopyroxene, clinopyroxene and garnet as structural OH [e.g. 1 ]. Considering the significant influence of hydrogen on mantle properties such as solidus temperature, rheology, conductivity and seismic velocity, it is important to understand both the distribution of water among mantle phases and the mass transfer processes that influence water distribution in the Earth's mantle. Despite the important role of water in the mantle, experimental determinations of the equilibrium distribution of trace amounts of hydrogen among coexisting silicate phases remain extremely limited. Improved analytical techniques have recently paved the way for quantitative investigations of water partitioning and abundances in nominally anhydrous mantle minerals [e.g. 2]. Several studies of submarine glasses have revealed correlated increases in incompatible elements and water contents along segments of mid-ocean ridges approaching hotspots [e.g. 3,4]. A source-related increase in the water content of the mantle is typically postulated to explain such observations, but elevated hotspot H2O contents may also relate to pressure differences in partitioning of water, analogous to the case for rare-earth elements (e.g. the "garnet signature"). New experimental water partitioning data illuminate these differences. Hydrogen isotope ratios vary in submarine glasses from ocean ridges, back-arc basins and hotspots, and in hydrous phases from arcs and hotspots, suggesting significant hydrogen isotopic variability in the mantle, which may be related to the subduction of water. Water clearly enters the upper mantle at subduction zones, however the full water budget for any single subduction zone is highly uncertain [e.g. 5]. This uncertainty in the water budget at convergent margins indicates that we do not even know whether the present-day net flux of water is into or out of the Earth. This talk will highlight areas of both knowledge and ignorance on the origin and distribution of water in the Earth's mantle. [1] Bell, D.R. & Rossman, G.R., 1992, Science, 255: 1391-1397. [2] Koga, K. et. al, 2002, Geochem. Geophys. Geosys. 4, doi: 10.1029/2002GC000378. [3] Dixon, J. E. et. al, 2002, Nature 420, 385-389. [4] Asimow, P. D. et. al, 2003, Geochem. Geophys. Geosys. 5, doi:10.1029/2003GC000568. [5] Hilton D. R.. et. al, 2002, in Noble Gases in Cosmochemistry and Geochemistry, 47:319-370.

Tracing ancient events in the lithospheric mantle: A case study from ophiolitic chromitites of SW Turkey

NASA Astrophysics Data System (ADS)

Akbulut, Mehmet; González-Jiménez, José María; Griffin, William L.; Belousova, Elena; O'Reilly, Suzanne Y.; McGowan, Nicole; Pearson, Norman J.

2016-04-01

New major-, minor- and trace-element data on high-Cr chromites from several ophiolitic podiform chromitites from Lycian and Antalya peridotites in southwestern Turkey reveal a polygenetic origin from a range of arc-type melts within forearc and back-arc settings. These forearc and the back-arc related high-Cr chromitites are interpreted to reflect the tectonic juxtaposition of different lithospheric mantle segments during the obduction. The diversity of the γOs(t=0) values (-8.28 to +13.92) in the Antalya and Lycian chromitite PGMs and their good correlations with the sub- to supra-chondritic 187Os/188Os ratios (0.1175-0.1459) suggests a heterogeneous mantle source that incorporated up to 40% recycled crust, probably due to subduction processes of the orogenic events. The few model ages calculated define two significant peaks in TRD model ages at 1.5 and 0.25 Ga, suggesting that the chromitites are younger than 0.25 Ga and include relics of an at least Mesoproterozoic or older (>1.0 Ga) mantle protolith. Eight of the nine zircon grains separated from the chromitites, are interpreted as detrital and/or resorbed xenocrystic relics, whilst a significantly less reworked/resorbed one is considered to be of metasomatic origin. In-situ U-Pb dating of the xenocrystic zircon grains yielded a spread of ages within ca 0.6-2.1 Ga, suggesting recycling of crustal rocks younger than 0.6 Ga (Late Neoproterozoic). The notable coincidence between the lower age limit of the older zircons (ca 1.6 Ga) and the oldest Os model age peak (ca 1.5 Ga) from the PGM may suggest a Mesoproterozoic rifting stage. These findings imply a Paleoproterozoic sub-continental lithospheric mantle (SCLM) protolith for the SW Anatolian mantle which was later converted into an oceanic lithospheric mantle domain possibly following a rifting and continental break-up initiated during Mesoproterozoic (ca 1.5-1.0 Ga). The single metasomatic zircon of ca 0.09 Ga age coinciding with the initiation of the contraction of the Neotethys may be interpreted to date the timing of a metasomatic event beneath the intra-oceanic subduction zone.

Water Content of Earth's Continental Mantle Is Controlled by the Circulation of Fluids or Melts

NASA Technical Reports Server (NTRS)

Peslier, Anne; Woodland, Alan B.; Bell, David R.; Lazarov, Marina; Lapen, Thomas J.

2014-01-01

A key mission of the ARES Directorate at JSC is to constrain models of the formation and geological history of terrestrial planets. Water is a crucial parameter to be measured with the aim to determine its amount and distribution in the interior of Earth, Mars, and the Moon. Most of that "water" is not liquid water per se, but rather hydrogen dissolved as a trace element in the minerals of the rocks at depth. Even so, the middle layer of differentiated planets, the mantle, occupies such a large volume and mass of each planet that when it is added at the planetary scale, oceans worth of water could be stored in its interior. The mantle is where magmas originate. Moreover, on Earth, the mantle is where the boundary between tectonic plates and the underlying asthenosphere is located. Even if mantle rocks in Earth typically contain less than 200 ppm H2O, such small quantities have tremendous influence on how easily they melt (i.e., the more water there is, the more magma is produced) and deform (the more water there is, the less viscous they are). These two properties alone emphasize that to understand the distribution of volcanism and the mechanism of plate tectonics, the water content of the mantle must be determined - Earth being a template to which all other terrestrial planets can be compared.

Halogen and trace element geochemistry in Mid-Ocean Ridge basalts from the Australian-Antarctic Ridge (AAR)

NASA Astrophysics Data System (ADS)

Yang, Y. S.; Seo, J. H.; Park, S. H.; Kim, T.

2015-12-01

Australian-Antarctic Ridge (AAR) is an extension of easternmost SE Indian Mid-Ocean Ridge (MOR).We collected volcanic glasses from the "in-axis" of the KR1 and KR2 MOR, and the overlapping zones of the KR1 MOR and the nearby seamounts ("KR1 mixing"). We determined trace and halogen elements in the glasses. Halogen concentrations and its ratios in the glasses are important to understand the mantle metasomatism and volatile recycling. 52 of the collected glasses are "primitive" (higher than 6 wt% MgO), while 3 of them have rather "evolved" composition (MgO wt% of 1.72, 2.95 and 4.15). K2O concentrations and Th/Sc ratios in the glasses show a negative correlation with its MgO concentration. Incompatible element ratios such as La/Sm are rather immobile during a magma differentiation so the ratios are important to understand mantle composition (Hofmann et al. 2003). La/Sm ratios in the glasses are 0.95 ~ 3.28 suggesting that the AAR basalts can be classified into T-MORB and E-MORB (Schilling et al., 1983). La/Sm ratios are well-correlated with incompatible elements such as U, Ba, Nb, and negatively correlated with compatible elements such as Sc, Eu2+, Mg. The AAR glasses contain detectable halogen elements. The "KR1 mixing" glasses in halogen elements are more abundant than "in-axis" the glasses. Cl is the least variable element compared to the other halogens such as Br and I in the AAR. The "KR1 mixing" glasses have the largest variations of Br/Cl ratios compared to the "in-axis" glasses. The Cl/Br and Th/Sc ratios in the "in-axis" glasses and in the "KR1 mixing" glasses show positive and negative correlations, respectively. The Br-rich glasses in the "KR1 mixing" zone might be explained by a recycled Br-rich oceanic slab of paleo-subduction or by a hydrothermal alteration in the AAR. I composition in the glasses does not show a correlation other trace elements. The K/Cl and K/Ti ratios in the AAR glasses are similar to the basalts from the Galapagos Spreading Center (Geldmacher et al., 2010) and Pacific MORB. The AAR region closely located with Balleny hotspot (Lanyon et al., 1993) and Pacific-Antarctic Ridge. K2O/Nb and Zr/Nb ratios are very low compared with near Pacific-Antarctic Ridge and Southeast Indian Ridge. The ratios are close to the Balleny hotspot.

Tracking the Depleted Mantle Signature in Melt Inclusions and Residual Glass of Basaltic Martian Shergottites using Secondary Ionization Mass Spectrometry

NASA Technical Reports Server (NTRS)

Peters, Timothy J.; Simon, Justin I.; Jones, John H.; Usui, Tomohiro; Economos, Rita C.; Schmitt, Axel K.; McKeegan, Kevin D.

2013-01-01

Trace element abundances of depleted shergottite magmas recorded by olivine-hosted melt inclusions (MI) and interstitial mesostasis glass were measured using the Cameca ims-1270 ion microprobe. Two meteorites: Tissint, an olivine-­phyric basaltic shergottite which fell over Morocco July 18th 2001; and the Antarctic meteorite Yamato 980459 (Y98), an olivine-phyric basaltic shergottite with abundant glassy mesostasis have been studied. Chondrite-­normalized REE patterns for MI in Tissint and Y98 are characteristically LREE depleted and, within analytical uncertainty, parallel those of their respective whole rock composition; supporting each meteorite to represent a melt composition that has experienced closed-­system crystallization. REE profiles for mesostasis glass in Y98 lie about an order of magnitude higher than those from the MI; with REE profiles for Tissint MI falling in between. Y98 MI have the highest average Sm/Nd and Y/Ce ratios, reflecting their LREE depletion and further supporting Y98 as one of our best samples to probe the depleted shergotitte mantle. In general, Zr/Nb ratios overlap between Y98 and Tissint MI, Ce/Nb ratios overlap between Y98 MI and mesostasis glass, and Sm/Nd ratios overlap between Y98 mesostasis glass and Tissint MI. These features support similar sources for both, but with subtle geochemical differences that may reflect different melting conditions or fractionation paths during ascent from the mantle. Interestingly, the REE patterns for both Y98 bulk and MI analyses display a flattening of the LREE that suggests a crustal contribution to the Y98 parent melt. This observation has important implications for the origins of depleted and enriched shergottites.

Redox Evolution in Magma Oceans Due to Ferric/Ferrous Iron Partitioning

NASA Astrophysics Data System (ADS)

Schaefer, L.; Elkins-Tanton, L. T.; Pahlevan, K.

2017-12-01

A long-standing puzzle in the evolution of the Earth is that while the present day upper mantle has an oxygen fugacity close to the QFM buffer, core formation during accretion would have occurred at much lower oxygen fugacities close to IW. We present a new model based on experimental evidence that normal solidification and differentiation processes in the terrestrial magma ocean may explain both core formation and the current oxygen fugacity of the mantle without resorting to a change in source material or process. A commonly made assumption is that ferric iron (Fe3+) is negligible at such low oxygen fugacities [1]. However, recent work on Fe3+/Fe2+ ratios in molten silicates [2-4] suggests that the Fe3+ content should increase at high pressure for a given oxygen fugacity. While disproportionation was not observed in these experiments, it may nonetheless be occurring in the melt at high pressure [5]. Therefore, there may be non-negligible amounts of Fe3+ formed through metal-silicate equilibration at high pressures within the magma ocean. Homogenization of the mantle and further partitioning of Fe2+/Fe3+ as the magma ocean crystallizes may explain the oxygen fugacity of the Earth's mantle without requiring additional oxidation mechanisms. We present here models using different parameterizations for the Fe2+/Fe3+ thermodynamic relationships in silicate melts to constrain the evolution of the redox state of the magma ocean as it crystallizes. The model begins with metal-silicate partitioning at high pressure to form the core and set the initial Fe3+ abundance. Combined with previous work on oxygen absorption by magma oceans due to escape of H from H2O [6], we show that the upper layers of solidifying magma oceans should be more oxidized than the lower mantle. This model also suggests that large terrestrial planets should have more oxidized mantles than small planets. From a redox perspective, no change in the composition of the Earth's accreting material needs to be invoked to explain mantle oxygen fugacity, although implications for trace elements in the Earth's core and mantle are still being explored. [1] Ringwood, AE (1979) [2] Armstrong, K et al (2016) LPSC, 2580 [3] Armstrong, K et al (2017) ACCRETE workshop [4] Zhang, HL et al (2017) GCA, 204, 83 [5] Frost, DJ et al (2004) Nature, 428, 409 [6] Schaefer, L et al (2016) ApJ, 829, 63

Geochemical Overview of the East African Rift System

NASA Astrophysics Data System (ADS)

Furman, T.

2003-12-01

Mafic volcanics of the East African Rift System (EARS) record a protracted history of continental extension that is linked to mantle plume activity. The modern EARS traverses two post-Miocene topographic domes separated by a region of polyphase extension in northern Kenya and southern Ethiopia. Basaltic magmatism commenced ˜45 Ma in this highly extended region, while the onset of plume-related activity took place ˜30 Ma with eruption of flood basalts in central Ethiopia. A spatial and temporal synthesis of EARS volcanic geochemistry shows progressive lithospheric removal (by erosion and melting) as the degree of rifting increases, with basalts in the most highly extended areas recording melting of depleted asthenosphere. Plume contributions are indicated locally in the northern half of the EARS, but are absent from the southern half. The geochemical signatures are compatible with a physical model in which the entire EARS is fed by a discontinuous plume emanating from the core-mantle boundary as the South African Superswell. Quaternary basaltic lavas erupted in the Afar triangle, Red Sea and Gulf of Aden define the geochemical signature attributed to the Afar plume (87Sr/86Sr 0.7034-0.7037, 143Nd/144Nd 0.5129-0.5130; La/Nb 0.6-0.9; Nb/U 40-50). These suites commonly record mixing with ambient upper mantle having less radiogenic isotopes but generally overlapping incompatible trace element abundances. Within the Ethiopian dome both lithospheric and sub-lithoshperic contributions can be documented clearly; lithospheric contributions are manifest in more radiogenic isotope values (87Sr/86Sr up to 0.7050) and distinctive trace element abundances (e.g., La/Nb <2.0, Nb/U > 10). The degree of lithospheric contribution is lowest within the active Main Ethiopian Rift and increases towards the southern margin of the dome. The estimated depth of melting (65-75 km) is consistent with geophysical observations of lithospheric thickness. In regions of prolonged volcanism the lithospheric contributions and estimated melting depths decrease through time, corresponding to a higher degree of rifting. In the Kenyan dome, including the western rift, the degree of extension is low and lithospheric melting is the dominant source for basaltic magmatism. Mafic lavas from these regions have generally lower MgO but higher contents of alkalis, P2O5 and many incompatible trace elements than are observed in the Ethiopian Rift. High values of 87Sr/86Sr, 207Pb/204Pb and Zr/Hf relative to other parts of the EARS indicate melting of metasomatized lithosphere. Melting in this area occurs at depths up to 100+ km, consistent with the thick crustal section observed seismically. Between the topographic domes, basalts from the Turkana region record melting at shallow levels ( ˜35 km) consistent with seismic evidence for nearly complete rifting of the crustal section. The geochemistry of these lavas is dominated by asthenospheric source materials, with only minor lithospheric involvement. Temporal evolution of EARS geochemistry reflects progressive rifting of the thick craton. This change is manifest within lavas that are interpreted as plume-derived, as Tb/Yb values decrease from 30 Ma through the present. The modern thermal anomaly associated with Afar volcanism does not appear to extend below the shallow mantle, but may reflect a large blob of deep mantle material that became stuck to Africa 30 Ma and has contributed to regional volcanism ever since. Relative contributions from this deep mantle source, shallow asthenosphere and lithosphere are controlled by the extent of rifting and cannot be predicted solely on the basis of surface topography.

Geochemistry of the Serifos calc-alkaline granodiorite pluton, Greece: constraining the crust and mantle contributions to I-type granitoids

NASA Astrophysics Data System (ADS)

Stouraiti, C.; Baziotis, I.; Asimow, P. D.; Downes, H.

2017-11-01

The Late Miocene (11.6-9.5 Ma) granitoid intrusion on the island of Serifos (Western Cyclades, Aegean Sea) is composed of syn- to post-tectonic granodiorite with quartz monzodiorite enclaves, cut by dacitic and aplitic dikes. The granitoid, a typical I-type metaluminous calcic amphibole-bearing calc-alkaline pluton, intruded the Cycladic Blueschists during thinning of the Aegean plate. Combining field, textural, geochemical and new Sr-Nd-O isotope data presented in this paper, we postulate that the Serifos intrusion is a single-zoned pluton. The central facies has initial 87Sr/86Sr = 0.70906 to 0.7106, ɛNd(t) = - 5.9 to - 7.5 and δ18Οqtz = + 10 to + 10.6‰, whereas the marginal zone (or border facies) has higher initial 87Sr/86Sr = 0.711 to 0.7112, lower ɛ Nd(t) = - 7.3 to - 8.3, and higher δ18Οqtz = + 10.6 to + 11.9‰. The small range in initial Sr and Nd isotopic values throughout the pluton is paired with a remarkable uniformity in trace element patterns, despite a large range in silica contents (58.8 to 72 wt% SiO2). Assimilation of a crustally derived partial melt into the mafic parental magma would progressively add incompatible trace elements and SiO2 to the evolving mafic starting liquid, but the opposite trend, of trace element depletion during magma evolution, is observed in the Serifos granodiorites. Thermodynamic modeling of whole-rock compositions during simple fractional crystallization (FC) or assimilation-fractional crystallization (AFC) processes of major rock-forming minerals—at a variety of pressure, oxidation state, and water activity conditions—fails to reproduce simultaneously the major element and trace element variations among the Serifos granitoids, implying a critical role for minor phases in controlling trace element fractionation. Both saturation of accessory phases such as allanite and titanite (at SiO2 ≥ 71 wt%)(to satisfy trace element constraints) and assimilation of partial melts from a metasedimentary component (to match isotopic data) must have accompanied fractional crystallization of the major phases.

[Trace elements in serum of malnourished and well-nourished children living in Lubumbashi and Kawama].

PubMed

Musimwa, Aimée Mudekereza; Kanteng, Gray Wakamb; Kitoko, Hermann Tamubango; Luboya, Oscar Numbi

2016-01-01

The role of trace metals elements in human nutrition can no longer be ignored. Deficiency caused by inadequate dietary intake, secondary deficiencies often under - estimated, and iatrogenic deficiencies lead to pathologies such as infections and others. For this reason their dosages are particularly important to assess disease severity and to facilitate early treatment or improve patient's diet. The aim of this study was to determine trace elements profile in blood (copper, selenium, zinc, iron, chromium, cobalt, etc.) among malnourished and well-nourished children in a mining community in Lubumbashi. Three hundred eleven cases have been collected, 182 malnourished children and 129 well-nourished children in a cross-sectional descriptive study conducted from July 2013 to December 2014. Exhaustive sampling was performed. Metal determination in serum was performed using Inductively Coupled Plasma Spectroscopy (ICP-OES/MS) in the laboratory at Congolese Control Office in Lubumbashi. Essential trace elements (copper, zinc, selenium and iron) were found at very low concentrations in both the malnourished and well-nourished children. Arsenic, cadmium, magnesium and manganese concentrations were normal compared with reference values in well-nourished children Antimony, chromium, lead and cobalt levels were high in both the malnourished and well-nourished children. Nickel level was normal malnourished and well-nourished children. Magnesium, manganese were found in very low levels in malnourished children. Both the malnourished and well-nourished children suffer from deficiencies of essential trace elements associated with trace metals elements This allows to assume that essential micronutrients deficiency promotes the absorption of heavy metals.

Two mantle sources, two plumbing systems: Tholeiitic and alkaline magmatism of the Maymecha River basin, Siberian flood volcanic province

USGS Publications Warehouse

Arndt, N.; Chauvel, C.; Czamanske, G.; Fedorenko, V.

1998-01-01

Rocks of two distinctly different magma series are found in a ???4000-m-thick sequence of lavas and tuffs in the Maymecha River basin which is part of the Siberian flood-volcanic province. The tholeiites are typical low-Ti continental flood basalts with remarkably restricted, petrologically evolved compositions. They have basaltic MgO contents, moderate concentrations of incompatible trace elements, moderate fractionation of incompatible from compatible elements, distinct negative Ta(Nb) anomalies, and ??Nd values of 0 to + 2. The primary magmas were derived from a relatively shallow mantle source, and evolved in large crustal magma chambers where they acquired their relatively uniform compositions and became contaminated with continental crust. An alkaline series, in contrast, contains a wide range of rock types, from meymechite and picrite to trachytes, with a wide range of compositions (MgO from 0.7 to 38 wt%, SiO2 from 40 to 69 wt%, Ce from 14 to 320 ppm), high concentrations of incompatible elements and extreme fractionation of incompatible from compatible elements (Al2O3/TiO2 ??? 1; Sm/Yb up to 11). These rocks lack Ta(Nb) anomalies and have a broad range of ??Nd values, from -2 to +5. The parental magmas are believed to have formed by low-degree melting at extreme mantle depths (>200 km). They bypassed the large crustal magma chambers and ascended rapidly to the surface, a consequence, perhaps, of high volatile contents in the primary magmas. The tholeiitic series dominates the lower part of the sequence and the alkaline series the upper part; at the interface, the two types are interlayered. The succession thus provides evidence of a radical change in the site of mantle melting, and the simultaneous operation of two very different crustal plumbing systems, during the evolution of this flood-volcanic province. ?? Springer-Verlag 1998.

Martian Igneous Geochemistry: The Nature of the Martian Mantle

NASA Technical Reports Server (NTRS)

Mittlefehldt, D. W.; Elkins-Tanton, L. T.; Peng, Z. X.; Herrin, J. S.

2012-01-01

Mafic igneous rocks probe the interiors of their parent objects, reflecting the compositions and mineralogies of their source regions, and the magmatic processes that engendered them. Incompatible trace element contents of mafic igneous rocks are widely used to constrain the petrologic evolution of planets. We focus on incompatible element ratios of martian meteorites to constrain the petrologic evolution of Mars in the context of magma ocean/cumulate overturn models [1]. Most martian meteorites contain some cumulus grains, but regardless, their incompatible element ratios are close to those of their parent magmas. Martian meteorites form two main petrologic/ age groupings; a 1.3 Ga group composed of clinopyroxenites (nakhlites) and dunites (chassignites), and a <1 Ga group composed of basalts and lherzolites (shergottites).

Sr-Nd-Pb isotopic constraints on the nature of the mantle sources involved in the genesis of the high-Ti tholeiites from northern Paraná Continental Flood Basalts (Brazil)

NASA Astrophysics Data System (ADS)

Rocha-Júnior, Eduardo R. V.; Marques, Leila S.; Babinski, Marly; Nardy, Antônio J. R.; Figueiredo, Ana M. G.; Machado, Fábio B.

2013-10-01

There has been little research on geochemistry and isotopic compositions in tholeiites of the Northern region from the Paraná Continental Flood Basalts (PCFB), one of the largest continental provinces of the world. In order to examine the mantle sources involved in the high-Ti (Pitanga and Paranapanema) basalt genesis, we studied Sr, Nd, and Pb isotopic systematics, and major, minor and incompatible trace element abundances. The REE patterns of the investigated samples (Pitanga and Paranapanema magma type) are similar (parallel to) to those of Island Arc Basalts' REE patterns. The high-Ti basalts investigated in this study have initial (133 Ma) 87Sr/86Sr ratios of 0.70538-0.70642, 143Nd/144Nd of 0.51233-0.51218, 206Pb/204Pb of 17.74-18.25, 207Pb/204Pb of 15.51-15.57, and 208Pb/204Pb of 38.18-38.45. These isotopic compositions do not display any correlation with Nb/Th, Nb/La or P2O5/K2O ratios, which also reflect that these rocks were not significantly affected by low-pressure crustal contamination. The incompatible trace element ratios and Sr-Nd-Pb isotopic compositions of the PCFB tholeiites are different to those found in Tristan da Cunha ocean island rocks, showing that this plume did not play a substantial role in the PCFB genesis. This interpretation is corroborated by previously published osmium isotopic data (initial γOs values range from +1.0 to +2.0 for high-Ti basalts), which also preclude basalt generation by melting of ancient subcontinental lithospheric mantle. The geochemical composition of the northern PCFB may be explained through the involvement of fluids and/or small volume melts related to metasomatic processes. In this context, we propose that the source of these magmas is a mixture of sublithospheric peridotite veined and/or interlayered with mafic components (e.g., pyroxenites or eclogites). The sublithospheric mantle (dominating the osmium isotopic compositions) was very probably enriched by fluids and/or magmas related to the Neoproterozoic subduction processes. This sublithospheric mantle region may have been frozen and coupled to the base of the Parana basin lithospheric plate above which the Paleozoic subsidence and subsequent Early Cretaceous magmatism occurred.

Density Sorting During the Evolution of Continental Crust

NASA Astrophysics Data System (ADS)

Kelemen, P. B.; Behn, M. D.; Hacker, B. R.

2015-12-01

We consider two settings - in addition to "delamination" of arc lower crust - in which dense, mafic eclogites founder into the convecting mantle while buoyant, felsic lithologies accumulate at the base of evolving continental crust. Arc processes play a central role in generating continental crust, but it remains uncertain how basaltic arc crust is transformed to andesitic continental crust. Dense, SiO2-poor products of fractionation may founder from the base of arc crust by "delamination", but lower arc crust after delamination has significantly different trace elements compared to lower continental crust (LCC). In an alternative model, buoyant magmatic rocks generated at arcs are first subducted, mainly via subduction erosion. Upon heating, these buoyant lithologies ascend through the mantle wedge or along a subduction channel, and are "relaminated" at
the base of overlying crust (e.g., Hacker et al EPSL 11, AREPS 15). Average buoyant lavas and plutons
for the Aleutians, Izu-Bonin-Marianas, Kohistan and Talkeetna arcs fall within the range of estimated LCC major and trace elements. Relamination is more efficient in generating continental crust than delamination. Himalayan cross-sections show Indian crust thrust beneath Tibetan crust, with no intervening mantle. There is a horizontal Moho at ca 80 km depth, extending from thickened Indian crust, across the region where Tibetan crust overlies Indian crust, into thickened Tibetan crust. About half the subducted Indian crust is present, whereas the other half is missing. Data (Vp/Vs; Miocene lavas formed by interaction of continental crust with mantle; xenolith thermometry) indicate 1000°C or more from ca 50 km depth to the Moho since the Miocene. We build on earlier studies (LePichon et al Tectonics 92, T'phys 97; Schulte-Pelkum et al Nature 05; Monsalve et al JGR 08) to advance the hypothesis that rapid growth of garnet occurs at 70-80 km and 1000°C within subducting Indian crust. Dense eclogites founder, while buoyant lithologies accumulate in thickening crust. Mantle return flow and radioactive heating in thick, felsic crust maintains high T. The crustal volume in this region grows at 760 m3/yr/m of strike length. Moho-depth earthquakes may be due to localized deformation and thermal runaway in weak layers and diapir margins.

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.

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.

Petrology and geochronology of lavas from Ka'ula Volcano: Implications for rejuvenated volcanism of the Hawaiian mantle plume

NASA Astrophysics Data System (ADS)

Garcia, Michael O.; Weis, Dominique; Jicha, Brian R.; Ito, Garrett; Hanano, Diane

2016-07-01

Marine surveying and submersible sampling of Ka'ula Volcano, located 100 km off the axis of the Hawaiian chain, revealed widespread areas of young volcanism. New 40Ar/39Ar and geochemical analyses of the olivine-phyric submarine and subaerial volcanic rocks show that Ka'ula is shrouded with 1.9-0.5 Ma alkalic basalts. The ages and chemistry of these rocks overlap with rejuvenated lavas on nearby, northern Hawaiian Island shields (Ni'ihau, Kaua'i and South Kaua'i Swell). Collectively, these rejuvenated lavas cover a vast area (∼7000 km2), much more extensive than any other area of rejuvenated volcanism worldwide. Ka'ula rejuvenated lavas range widely in alkalinity and incompatible element abundances (e.g., up to 10× P2O5 at a given MgO value) and ratios indicating variable degrees of melting of a heterogeneous source. Heavy REE elements in Ka'ula lavas are pinned at a mantle normalized Yb value of 10 ± 1, reflecting the presence of garnet in the source. Trace element ratios indicate the source also contained phlogopite and an Fe-Ti oxide. The new Ka'ula ages show that rejuvenated volcanism was nearly coeval from ∼0.3 to 0.6 Ma along a 450 km segment of the Hawaiian Islands (from West Maui to north of Ka'ula). The ages and volumes for rejuvenated volcanism are inconsistent with all but one geodynamic melting model proposed to date. This model advocates a significant contribution of pyroxenite to rejuvenated magmas. Analyses of olivine phenocryst compositions suggest a major (33-69%) pyroxenite component in Ka'ula rejuvenated lavas, which correlates positively with radiogenic Pb isotope ratios for Ka'ula. This correlation is also observed in lavas from nearby South Kaua'i lavas, as was reported for Atlantic oceanic islands. The presence of pyroxenite in the source may have extended the duration and volume of Hawaiian rejuvenated volcanism.

Plagioclase-free Back-Arc Basalts from Caviahue, Argentina

NASA Astrophysics Data System (ADS)

Hesse, A.; Varekamp, J. C.

2006-12-01

Back-arc basalts and basaltic andesites occur in a N-S oriented graben east of the Copahue Caviahue volcanic complex, Province of Neuquen, Argentina. Lava flows and cinder cones are recent features of the modern topography and probably are of Pleistocene-Holocene age. Samples were collected along a 200 km stretch between Zapala and El Huecu. Lava and scoria samples from the Laguna Blanca and Zapala region have MgO contents up to 8.5 %, with Cr and Ni resp. at 250 and 180 ppm. These rocks carry olivine with small spinel inclusions, rare clinopyroxene, but lack plagioclase phenocrysts. Further north, andesitic samples occur with two pyroxenes and plagioclase. Major and trace element analyses show normal increases in incompatible elements with decreasing MgO for the more evolved group of samples. The more Mg-rich samples, however, show variable enrichments in K, Ba (up to 400 ppm) and other incompatible elements, but lack negative Nb anomalies. The plagioclase-free rocks lack negative Eu anomalies and have up to 750 ppm Sr. The whole rock suite (from 2.1-8.5 % MgO) has a Th/U ratio of ~4, Sm/Yb ~2.5 and La/Sm ~ 3.5. Sr and Nd isotope data of a cinder cone sample (5.5 % MgO, distinct negative Nb anomaly) are just outside the N-MORB field, resp. at 0.703295 and 0.512924 (Varekamp et al., GSA Spec Paper 407, 2006). We tentatively interpret these rocks as melts from a mantle with variable contributions of a heavily fractionated residue of subducted sediment and ocean floor, which have subsequently undergone some crystal fractionation. The suppression of plagioclase crystallization may result from water added to the back arc mantle region from the subducted complex, but the typical arc signatures such as negative Nb anomalies are lacking in these rocks.

Inclusions of Sulphide Immiscible Melts in Primitive Olivine Phenocrysts from Mantle-Derived Magmas; Preliminary Results

NASA Astrophysics Data System (ADS)

Danyushevsky, L.; Ryan, C.; Kamenetsky, V.; Crawford, A.

2001-12-01

Sulphide inclusions have been identified in olivine phenocrysts (and in one case in a spinel phenocryst) in primitive volcanic rocks from mid- ocean ridges, subduction-related island arcs and backarc basins. These inclusions represent droplets of an immiscible sulphide melt and are trapped by olivine crystals growing from silicate melts. Sulphide melt is usually trapped as separate inclusions, however combined inclusions of sulphide and silicate melts have also been observed. Sulphide inclusions have rounded shapes and vary in size from several up to 100 microns in diameter. At room temperature sulphide inclusions consist of several phases. These phases are formed as a result of crystallisation of the sulphide melt after it was trapped. Crystallisation occurs due to decreasing temperature in the magma chamber after trapping and/or when magma ascents from the magma chamber during eruptions. In all studied sulphides three different phases can be identified: a high- Fe, low-Ni, low-Cu phase; a high-Fe, high-Ni, low-Cu phase; and high-Fe, low-Ni, high-Cu phase. Low-Cu phases appear to be monomineralic, whereas the high-Cu phase is usually composed of a fine intergrowth of high- and low-Cu phases, resembling the quench 'spinifex' structure. Fe, Ni and Cu are the major elements in all sulphides studied. The amount of Ni decreases with decreasing forsterite content of the host olivine phenocryst, which is an index of the degree of silicate magma fractionation. Since Ni content of the silicate magma is decreasing during fractionation, this indicates either that the immiscible sulfide melt remains in equilibrium with the silicate melt continuously changing its composition during fractionation, or that the sulfide melt is continuously separated from the silicate melt during fractionation, with later formed droplets having lower Ni content due to the lower Ni content of the evolved, stronger fractionated silicate melt. Trace element contents of the sulfide inclusions have been analysed on the proton microprobe at CSIRO in Sydney. The main trace elements in the sulfide inclusions are Zn, Pb, Ag, and Se. Other trace elements are below detection limits, which are normally at a level of several ppm. Zn concentrations (120 +/- 40 ppm) in sulphides are similar to those in silicate melts. This indicates that separation of the sulfide melt does not affect Zn contents of silicate melts. On the contrary, Ag (30 +/- 10 ppm) and Pb (40 +/- 10 ppm) contents in sulphides are at least in order of magnitude higher than in the silicate melt, and thus separation of the immiscible sulfide melt can significantly decrease Pb and Ag contents of the silicate magma. The widespread occurrence of sulfide inclusions, which were also described in olivine phenocrysts from ocean island basalts, indicates common saturation at low pressure of mantle-derived magmas with reduced sulfur.

Back arc basalts from Patagonia: sediment input in a distal subduction domain

NASA Astrophysics Data System (ADS)

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

2007-12-01

Cinder cones and lava flows from the Loncopue graben in N Patagonia (37 S) were sampled over a 180 km N-S transect. These mainly basaltic and trachybasaltic lava flows carry olivine with Cr-Al-rich spinel inclusions, while some more evolved flows carry clinopyroxene and plagioclase. Most of these rocks have between 5-8 percent MgO, and show highly variable K and LIL trace element concentrations. The rocks have up to 180 ppm Ni and 250 ppm Cr. Relative trace element abundance diagrams show negative Ta-Nb anomalies in most rocks, although their depths vary strongly. The REE patterns show LREE enrichment and most rocks have no Eu anomalies, indicating the absence of significant plagioclase fractionation. The basalts have constant U/Th values (~0.25) that are similar to those found in the nearby Copahue-Caviahue arc volcanics. Microprobe analyses of the main phases show olivine with Mg # of 80-87 and up to 2600 ppm Ni. Simulations with the Melts-pMelts programs and application of mineral-melt geothermometers suggest that most olivine phenocrysts crystallized at ~8-10 kbar pressure at temperatures of 1170-1220 oC and with 1-3 percent H2O in the melt. The Sr isotope compositions of 9 samples show a range from 0.7033 - 0.7043, which are negatively correlated with Nd isotope ratios (0.51273- 0.51292). Surprisingly, the most MgO-rich basalt has the most radiogenic Sr isotope ratio. The Pb isotope ratios, well outside the DMM range, correlate very poorly with either Sr isotope ratios or in Pb-Pb isotope graphs. The lack of correlation between degree of evolution and Sr isotope ratios as well as the primitive nature of the rocks and crystals suggest that crustal assimilation was not a major process impacting the composition of these small magma volumes. Incompatible trace element patterns of several samples resemble those of detrital sediment samples from the Pacific, which together with the isotopic data suggest that these magmas may carry a subducted sediment component. Trace element concentrations and ratios do not correlate with radiogenic isotope ratios, suggesting that more than one contaminant source impacted the mantle domain, e.g., fluids as well as sediment melts. Isotope and trace element ratios vary considerably between cinder cones that are only 10-15 km apart, suggesting that the underlying mantle is highly heterogeneous, enriched in subducted components in thin veins and patches. The Loncopue basalts seem to be transitional in composition between the very voluminous S-Patagonia back-arc basalts and the Copahue-Caviahue arc rocks to the north.

Geochemical and Fluid Dynamic Investigations into the Nature of Chemical Heterogeneity in the Earth’s Mantle

DTIC Science & Technology

1992-09-01

21 ’ N on the East Pacific Rise . Earth Planet. Sci. Lett., 65, 17-33. Newsom, H. E., W. M. White, K. P. Jochum and A. W...peridotites. In addition, abyssal peridotites from the fast-spreading East Pacific Rise have not been analyzed for their trace element compositions. Given...Garcia, and D.W. Muenow (1986) Volatiles in basaltic glasses from the East Pacific Rise at 2 IN: implications for MORB sources and submarine lava

Relationship between Famatinian Arc Magmatism and Recent Mafic Volcanism in Northwest Argentina: Implications for Lithospheric Composition and Evolution Beneath the Puna Plateau

NASA Astrophysics Data System (ADS)

Drew, S.; Schoenbohm, L.; Ducea, M.

2008-12-01

The tectonic and magmatic evolution of the Puna Plateau (NW Argentina) has generated much debate over the past two decades. This study focuses on the young (< 7 Ma), mafic magmatism that led to the creation of monogenetic and simple polygenetic volcanoes throughout the plateau. These volcanics provide a means to evaluate the recent petro-tectonic development of the plateau and, in combination with Ordovician intrusive rocks, determine the isotopic composition and long term evolution of the sub-continental lithospheric mantle (SCLM) beneath the Andean back-arc domain. Here we present new whole rock major and trace element data and isotopic values for volcanic samples collected from the Antofagasta and Pasto Ventura basins in the southern Puna Plateau. Major element chemistry shows most of our samples are basalt, trachybasalt, basaltic andesite and basaltic trachyandesites, some with < 50.0 wt% SiO2 and > 8.0 wt% MgO, which is indicative of a strong mantle component. The more primitive lavas likely have a sub-crustal origin and experienced minimal interaction with overlying crust during transport to the surface. Two of our samples with low wt% MgO, a silicic andesite and a dacite, indicate an extensive crustal component and possibly a lower crust origin for evolved magmas. All samples have light trace element enrichment compared to NMORB and elevated abundances of LIL and LRE elements compared to HFS and HRE elements, indicating the magmas originated from a metasomatized source region. The samples also have variable (low and high) Nb, Ta and Ti negative anomalies, which are interpreted to be a signature of the source region. Our samples do not have a lithospheric delamination (~OIB) trace element signature as proposed by previous workers in support of a delamination model. Additionally, the samples have isotopic values (e.g. 87Sr/86Sr >0.7055 and ɛNd <0) that are not comparable to depleted asthenosphere. It is impossible for asthenospheric magma to obtain these isotopic values through crustal assimilation or AFC processes while maintaining a basalt major element composition and high Ni and Cr concentrations. Therefore, we propose the mafic magmas are sourced from a SCLM that, in accord with the LIL and LRE element concentrations, has been metasomatized during dehydration and possibly melting of a subducting oceanic plate. The young volcanics have isotopic values nearly identical to those of Early Ordovician Famatinian gabbros and norites. We suggest the most primitive Puna volcanic and Famatinian samples originated from the same SCLM source region. This implies at least a thin portion of the SCLM has remained intact beneath NW Argentina for the last ~485 million years. Resultantly, the SCLM was likely thinned to its present thickness sometime between the Early Ordovician and the Late Miocene. Thinning may have occurred by long term mantle wedge processes. Steady shortening and thickening of the continental crust and gradual removal of the SCLM by convection is envisioned here. The occurrence of discrete, intermittent delamination events is not favored because removal and then regeneration of the SCLM would not have allowed for preservation of the Famatinian isotopic signature.

Calcio-carbonatite melts and metasomatism in the mantle beneath Mt. Vulture (Southern Italy)

NASA Astrophysics Data System (ADS)

Rosatelli, Gianluigi; Wall, Frances; Stoppa, Francesco

2007-12-01

At Mt. Vulture volcano (Basilicata, Italy) calcite globules (5-150 μm) are hosted by silicate glass pools or veins cross-cutting amphibole-bearing, or more common spinel-bearing mantle xenoliths and xenocrysts. The carbonate globules are rounded or elongated and are composed of a mosaic of 2-20 μm crystals, with varying optical orientation. These features are consistent with formation from a quenched calciocarbonatite melt. Where in contact with carbonate amphibole has reacted to form fassaitic pyroxene. Some of these globules contain liquid/gaseous CO 2 bubbles and sulphide inclusions, and are pierced by quench microphenocrysts of silicate phases. The carbonate composition varies from calcite to Mg-calcite (3.8-5.0 wt.% MgO) both within the carbonate globules and from globule to globule. Trace element contents of the carbonate, determined by LAICPMS, are similar to those of carbonatites worldwide including ΣREE up to 123 ppm. The Sr-Nd isotope ratios of the xenolith carbonate are similar to the extrusive carbonatite and silicate rocks of Mt. Vulture testifying to derivation from the same mantle source. Formation of immiscibile silicate-carbonatite liquids within mantle xenoliths occurred via disequilibrium immiscibility during their exhumation.

Garnet Signatures in Geophysical and Geochemical Observations: Insights into the Thermo-Petrological Structure of Oceanic Upper Mantle

NASA Astrophysics Data System (ADS)

Grose, C. J.; Afonso, J. C.

2013-12-01

We have developed new physically comprehensive thermal plate models of the oceanic lithosphere which incorporate temperature- and pressure-dependent heat transport properties and thermal expansivity, melting beneath ridges, hydrothermal circulation near ridge axes, and insulating oceanic crust. These models provide good fits to global databases of seafloor topography and heat flow, and seismic evidence of thermal structure near ridge axes. We couple these thermal plate models with thermodynamic models to predict the petrology of oceanic lithosphere. Geoid height predictions from our models suggest that there is a strong anomaly in geoid slope (over age) above ~25 Ma lithosphere due to the topography of garnet-field mantle. A similar anomaly is also present in geoid data over fracture zones. In addition, we show that a new assessment of a large database of ocean island basalt Sm/Yb systematics indicates that there is an unmistakable step-like increase in Sm/Yb values around 15-20 Ma, indicating the presence of garnet. To explain this feature, we have attempted to couple our thermo-petrological models of oceanic upper mantle with an open system, non-modal, dynamic melting model with diffusion kinetics to investigate trace element partitioning in an ascending mantle column.

Assessment of relative Ti, Ta, and Nb (TiTaN) enrichments in global ocean island basalts

NASA Astrophysics Data System (ADS)

Peters, B.; Day, J. M.

2013-12-01

The relative sensitivity of trace element concentrations to processes governing solid-melt and solid-fluid interactions has made them particularly useful for tracing the effects of partial melting, fractional crystallization, metasomatism and similar processes on the composition of a parental melt to a rock or mineral. Radiogenic and stable isotope compositions, in contrast, can provide information on the long-term history and provenance of magmas. Despite the distinct information derived from relative and absolute abundances of trace elements compared with isotopes, numerous studies of ocean island basalts (OIB) have attempted to use trace elements as diagnostic geochemical tracers to understand parental magma compositions. In particular, attempts have been made to correlate 'TiTaN' (Ti, Ta and Nb) anomalies to the He-Os isotopic compositions of OIB based on contributions from recycled eclogite, a theoretical high-TiTaN reservoir, and peridotite, a theoretical high-3He/4He reservoir (Jackson, et al., 2008 G-cubed). These authors have proposed that TiTaN anomalies can be used as independent indicators for recycled oceanic crust and lithospheric mantle in OIB sources, a distinction previously reserved for isotopic data. However, TiTaN anomalies appear uncorrelated to OIB mantle source composition for three reasons. First, a new geochemical compilation of global OIB shows a wide range of Ti (Ti/Ti* = 0.28 - 2.35), Ta (Ta/Ta* = 0.11 - 93.42) and Nb (Nb/Nb* = 0.13 - 17.79) anomalies that do not correlated with each other or noble gas systematics, indicating that: (i) TiTaN anomalies alone do not correspond to the primitive source traced by high-3He/4He or the solar neon component and (ii) Ti, Ta and Nb anomalies may each reflect distinct processes or origins, rather than tracing a single source or process together. Second, positive Ti anomalies can be generated by low-degree (1-10%), non-modal batch partial melting of garnet lherzolite at temperatures and pressures thought to be typical for OIB in many settings (T = 1075 - 1420 °C; P = 1 - 3.5 GPa). Furthermore, Ti, Ta and Nb anomalies can be theoretically created by subjecting the same low-degree partial melt to shallow level assimilation-fractional crystallization processes. If TiTaN anomalies are derived from this ubiquitous process, it presents a challenge to their origin from recycled or deep mantle parental materials. Finally, because clinopyroxene can contain large positive Ti anomalies (up to Ti/Ti* ≈ 1000), clinopyroxene accumulation can result in apparent high positive Ti/Ti* anomalies in ankaramites or other clinopyroxene-bearing rocks, when in reality, these Ti anomalies have been generated independent of primary source composition. Current evidence suggests that TiTaN anomalies do not directly reflect distinct source components in OIB lavas. Even if Ti, Ta and/or Nb enrichments are systematically present in high-3He/4He OIB parental materials, it is unlikely they are preserved due to magma processing at shallow depths.

Posterior Cord Syndrome and Trace Elements Deficiency as an Uncommon Presentation of Common Variable Immunodeficiency

PubMed Central

dos Santos Mota, Ananda; Morais Monteiro, Priscila; Carvalho, Angela Cristina Gouvêa; Fernandes Diniz, Barbara; Gemal Lanzieri, Pedro; Carneiro Ramos, Ricardo; Mocarzel, Luis Otavio

2017-01-01

Diarrhea is one of the most common symptoms in common variable immunodeficiency, but neurologic manifestations are rare. We presented a 50-year-old woman with recurrent diarrhea and severe weight loss that developed a posterior cord syndrome. Endoscopy found a duodenal villous blunting, intraepithelial lymphocytosis, and lack of plasma cells and magnetic resonance imaging of the spine was normal. Laboratory assays confirmed common variable immunodeficiency syndrome and showed low levels of trace elements (copper and zinc). Treatment was initiated with parenteral replacement of trace elements and intravenous human immunoglobulin and the patient improved clinically. In conclusion, physicians must be aware that gastrointestinal and neurologic disorders may be related to each other and remember to request trace elements laboratory assessment. PMID:28356913

Magnesium Isotopic Compositions of Continental Basalts From Various Tectonic Settings

NASA Astrophysics Data System (ADS)

Yang, W.; Li, S.; Tian, H.; Ke, S.

2016-12-01

Recycled sedimentary carbonate through subduction is the main light Mg isotopic reservoir in Earth's deep interior, thus Mg isotopic variation of mantle-derived melts provides a fresh perspective on investigating deep carbon cycling. Here we investigate Mg isotopic compositions of continental basalts from various tectonic settings: (1) The Cenozoic basalts from eastern China, coinciding with the stagnant Pacific slab in the mantle transition zone revealed by seismic tomography; (2) The Cenozoic basalts from Tengchong area, southwestern China, which comprises a crucial part of the collision zone between the Indian and Eurasian plates; (3) The Permian basalts from Emeishan large igneous province, related to a mantle plume. The Cenozoic basalts from both eastern China and Tengchong area exhibit light Mg isotopic compositions (δ26Mg = -0.60 to -0.30‰ and -0.51 to -0.33‰), suggesting recycled sedimentary carbonates in their mantle sources. This is supported by their low Fe/Mn, high CaO/Al2O3, low Hf/Hf* and low Ti/Ti* ratios, which are typical features of carbonated peridotite-derived melt. The Tengchong basalts also show high 87Sr/86Sr, high radiogenic Pb and upper crustal-like trace element pattern, indicating contribution of recycled continental crustal materials. By contrast, all Emeishan basalts display a mantle-like Mg isotopic composition, with δ26Mg ranging from -0.35 to -0.19‰. Since the Emeishan basalts derived from a mantle plume, their mantle-like Mg isotopic composition may indicate limited sedimentary carbonated recycled into the lower mantle. This is consistent with a recent experimental study which concluded that direct recycling of carbon into the lower mantle may have been highly restricted throughout most of the Earth's history.

Geochemistry and Pb Isotopes from the Jan Mayen Fracture Zone and the Extinct Aegir Ridge

NASA Astrophysics Data System (ADS)

Sayit, K.; Hanan, B. B.; Ito, G.; Howell, S. M.; Vogt, P. R.; Breivik, A. J.; Mjelde, R.; Pedersen, R. B.; Arrgh Scientific Team

2011-12-01

The Aegir Ridge appears as a major gap or "hole" in the N-Atlantic LIP, created by the Iceland hotspot. The Aegir Ridge created anomalously thick crust (8-11 km) during the first 2-4 Myr spreading, followed by a decrease in magma production and crustal thickness of 3.5-6 km (51.4-25 Ma). Possible explanations are, the lithospheric structure of the newly rifting Kolbeinsey Ridge and Jan Mayen micro-continent diverted mantle flow from the hotspot away from Aegir Ridge, and/or plume flux was low at that time. We report trace element and Pb isotope results for basalts dredged from the Jan Mayen FZ and Aegir Ridge flanks ~69-64 °N. Dredges returned Mn crust, erratic cobbles, hyaloclastite, and basalt diabase. Trace elements reveal distinct chemical groups, including very-depleted melts with very high Zr/Nb ratios (60.7) at one end, and melts of highly enriched characteristics on the other (2.7). The very-depleted compositions show significant LREE depletion relative to HREE [Ce/Yb]N=0.3), while the highly enriched compositions show LREE enrichment [Ce/Yb]N=2.2. Th/Nb ratios vary between 0.07-0.49, indicating variable Th enrichment. Trace element systematics indicate that between group elemental variations can't be solely explained by fractional crystallization and/or partial melting, the observed variations are largely source-related. Trace element systematics are consistent with a mixed MORB/OIB/SCLM mantle source, where relatively enriched samples resemble Faeroe Island lavas, and depleted ones are akin to Kolbeinsey Ridge lavas. Jan Mayen FZ rocks have initial (40Ma) 206Pb/204Pb: 207Pb/204Pb: 208Pb/204Pb =18.2-18.57:15.47-15.54:37.83-38.46 and AR, 16.59-18.75:15.16-15.53:37:36.62-38.51. Jan Mayen FZ, and Aegir Ridge samples with 206Pb/204Pb > 18.2 have higher 207Pb/204Pb and 208Pb/204Pb than the Iceland Neovolcanic lavas and are similar to the Iceland Tertiary and anomalous Öræfajökull basalts. Aegir Ridge basalts with 206Pb/204Pb <17.5 plot below the NHRL in the 206Pb/204Pb vs 207Pb/204Pb and above it in the 206Pb/204Pb vs 208Pb/204Pb diagrams, a characteristic of the British Tertiary Province basalts formed during the early stages of opening of the North Atlantic. We can't be certain that the dredged samples represent primary Aegir Ridge material, or if they were derived from elsewhere along the Iceland-Faeroe Ridge (eg, Faeroes), and transported to the dredge locations. If these rocks were erupted at the Aegir Ridge, the data show that at this time the ambient N-Atlantic upper mantle was relatively uncontaminated by the Iceland Plume, but significantly polluted by continental material, presumably during the early opening of the N-Atlantic Ocean Basin. ARRGH Cruise Scientific Team: Rolf Mjelde, Rolf Birger Pedersen, Helene Kraft, Marcus Fink, Ernst Flüh

Zircon U-Pb age, Hf isotope and geochemistry of Carboniferous intrusions from the Langshan area, Inner Mongolia: Petrogenesis and tectonic implications

NASA Astrophysics Data System (ADS)

Liu, Min; Zhang, Da; Xiong, Guangqiang; Zhao, Hongtao; Di, Yongjun; Wang, Zhong; Zhou, Zhiguang

2016-04-01

Late Paleozoic was a critical period for the tectonic evolution of the northern margin of the Alxa-North China craton, but the evolutionary history is not well constrained. The Carboniferous intrusions in the Langshan area in the western part of the northern margin of the Alxa-North China craton are mainly composed of tonalite, quartz diorite, olivine gabbro and pyroxene peridotite. Zircon LA-ICP-MS U-Pb dating indicates that the Langshan Carboniferous intrusions were emplaced at ca. 338-324 Ma. The quartz diorites are characterized by high amounts of compatible trace elements (Cr, Ni and V) and high Mg# values, which may suggest a significant mantle source. The positive Pb and negative Nb-Ta-Ti anomalies, the variable εHf(t) (-6.9 to 2.0) values and the old Hf model ages (1218-1783 Ma) imply some involvement of ancient continental materials in its petrogenesis. The tonalite has relatively high Sr/Y ratios, low Mg#, Yb and Y contents, features of adakite-like rocks, negative εHf(t) values (-9.8 to -0.1) and older Hf model ages (1344-1953 Ma), which suggest significant involvement of ancient crust materials and mantle-derived basaltic component in its petrogenesis. The high Mg# values, high Cr and Ni contents, and low Zr and Hf contents of the mafic-ultramafic rocks show evidence of a mantle source, and the relatively low zircon εHf(t) values (-5.9 to 3.2) might point to an enriched mantle. The trace element characteristics indicate the influence of subducted sediments and slab-derived fluids. In the tectonic discrimination diagrams, all the rocks plot in subduction-related environment, such as volcanic arc and continental arc. Considering the regional geology, we suggest that the Carboniferous intrusions in the Langshan area were likely emplaced during the late stage of the southward subduction of the Paleo-Asian Ocean plate, which formed a continental arc along the northern margin of the Alxa-North China craton.

Compositional variation through time and space in Quaternary magmas of the Chyulu Hills Volcanic Province, Kenya

NASA Astrophysics Data System (ADS)

Widom, E.; Kuentz, D. C.

2017-12-01

The Chyulu Hills Volcanic Province, located in southern Kenya >100 km east of the Kenya Rift Valley, has produced mafic, monogenetic eruptions throughout the Quaternary. The volcanic field is considered to be an off-rift manifestation of the East African Rift System, and is known for the significant compositional variability of its eruptive products, which range from nephelinites to basanites, alkali basalts, hawaiites, and orthopyroxene-normative subalkaline basalts [1]. Notably, erupted compositions vary systematically in time and space: Pleistocene volcanism, occurring in the northern Chyulu Hills, was characterized by highly silica-undersaturated magmas, whereas Holocene volcanism, restricted to the southern Chyulu Hills, is less silica-understaturated, consistent with a progressive decrease in depth and increase in degree of melting with time, from north to south [1]. Pronounced negative K anomalies, and enriched trace element and Sr-Nd-Pb isotope signatures have been attributed to a metasomatized, amphibole-bearing, sub-continental lithospheric mantle (SCLM) source [2]. Seismic evidence for a partially molten zone in the SCLM beneath this region [3] may be consistent with such an interpretation. We have analyzed Chyulu Hills samples for Os, Hf and high precision Pb isotopes to further evaluate the magma sources and petrogenetic processes leading to systematic compositional variation in time and space. Sr-Nd-Pb-Hf isotope systematics and strong negative correlations of 206Pb/204Pb and highly incompatible trace element ratios with SiO2 are consistent with the progression from a deeper, HIMU-type source to a shallower, EM-type source. Os isotope systematics, however, suggest a more complex relationship; although all samples are more radiogenic than primitive mantle, the least radiogenic values (similar to primitive OIB) are found in magmas with intermediate SiO2, and those with lower or higher SiO2 are more radiogenic. This may be explained by interaction between mantle plume-derived magmas and heterogeneous metasomatized SCLM, consistent with the radiogenic Os isotope compositions found in some highly metasomatized mantle xenoliths associated with the Tanzanian craton [4]. [1] Spath et al., 2000; [2] Spath et al., 2001; [3] Ritter & Kasper, 1997; [4] Nelson et al., 2012.

Geochemical distribution of major and trace elements in agricultural soils of Castilla-La Mancha (central Spain): finding criteria for baselines and delimiting regional anomalies.

PubMed

Bravo, Sandra; García-Ordiales, Efrén; García-Navarro, Francisco Jesús; Amorós, José Ángel; Pérez-de-Los-Reyes, Caridad; Jiménez-Ballesta, Raimundo; Esbrí, José María; García-Noguero, Eva María; Higueras, Pablo

2017-09-07

Castilla-La Mancha (central Spain) is a region characterized by significant agricultural production aimed at high-quality food products such as wine and olive oil. The quality of agricultural products depends directly on the soil quality. Soil geochemistry, including dispersion maps and the recognition of baselines and anomalies of various origins, is the most important tool to assess soil quality. With this objective, 200 soil samples were taken from agricultural areas distributed among the different geological domains present in the region. Analysis of these samples included evaluation of edaphological parameters (reactivity, electrical conductivity, organic matter content) and the geochemistry of major and trace elements by X-ray fluorescence. The dataset obtained was statistically analyzed for major elements and, in the case of trace elements, was normalized with respect to Al and analyzed using the relative cumulative frequency (RCF) distribution method. Furthermore, the geographic distribution of analytical data was characterized and analyzed using the kriging technique, with a correspondence found between major and trace elements in the different geologic domains of the region as well as with the most important mining areas. The results show an influence of the clay fraction present in the soil, which acts as a repository for trace elements. On the basis of the results, of the possible elements related with clay that could be used for normalization, Al was selected as the most suitable, followed by Fe, Mn, and Ti. Reference values estimated using this methodology were lower than those estimated in previous studies.

Diogenites: Cumulates from Asteroid 4 Vesta: Insights from Orthopyroxene and Spinel Chemistry

NASA Technical Reports Server (NTRS)

Papike, James J.; Bowman, L. E.; Spilde, M. N.; Fowler, G. W.; Shearer, C. K.

1996-01-01

Cumulate rocks are important planetary lithologies, but they can be difficult to interpret. Important clues to the nature of their parental melts may still be present in the interiors of cumulus phases. However, in some cases, even the cores of the cumulus grains may have been modified by postcrystallization reactions with trapped melt and other cumulus phases. We have previously studied the major-, minor-, and trace-element chemistry of orthopyroxene from a suite of diogenites and concluded that their chemical attributes can best be explained by crystallization from parental melts that were derived from a depleted mantle source that had already experienced eucrite removal. However, we and others have had difficulty explaining the great range in concentration of minor elements (Al, Ti) and trace elements (REE, Y, Zr) if all diogenites were derived from a single magmatic system. Therefore, we have investigated the chemistry of diogenitic spinels to see if they still held clues to the diogenite parental melt compositions. Although spinel is low in abundance in diogenites (<5 vol%) it still may hold clues to the maomatic and metamorphic history of these rocks.

Assessment of the effects of glutamic acid decarboxylase antibodies and trace elements on cognitive performance in older adults.

PubMed

Alghadir, Ahmad H; Gabr, Sami A; Al-Eisa, Einas S

2015-01-01

Homeostatic imbalance of trace elements such as iron (Fe), copper (Cu), and zinc (Zn) demonstrated adverse effects on brain function among older adults. The present study aimed to investigate the effects of trace elements and the presence of anti-glutamic acid decarboxylase antibodies (GADAs) in human cognitive abilities among healthy older adults. A total of 100 healthy subjects (65 males, 35 females; age range; 64-96 years) were recruited for this study. Based on Loewenstein Occupational Therapy Cognitive Assessment (LOTCA) score, the participants were classified according to cognitive performance into normal (n=45), moderate (n=30), and severe (n=25). Cognitive functioning, leisure-time physical activity (LTPA), serum trace elements - Fe, Cu, Zn, Zn/Cu, and GADAs were assessed using LOTCA battery, pre-validated physical activity (PA) questionnaire, atomic absorption, and immunoassay techniques, respectively. Approximately 45% of the study population (n=45) had normal distribution of cognitive function and 55% of the study population (n=55) had abnormal cognitive function; they were classified into moderate (score 62-92) and severe (score 31-62). There was a significant reduction in the level of Zn and Zn/Cu ratio along with an increase in the level of Fe, Cu, and anti-GADAs in subjects of severe (P=0.01) and moderate (P=0.01) cognitive performance. LOTCA-cognitive scores correlated positively with sex, HbA(1c), Fe, Cu, Zn, and Zn/Cu ratio, and negatively with age, PA, body mass index, and anti-GADAs. Significant inter-correlation was reported between serum trace element concentrations and anti-GADAs which suggest producing a cognitive decline via oxidative and neural damage mechanism. This study found significant associations among trace elements, anti-GADAs, and cognitive function in older adults. The homeostatic balance of trace elements should be recommended among older adults for better cognitive performance.

Reactive transport in a partially molten system with binary solid solution

NASA Astrophysics Data System (ADS)

Jordan, J.; Hesse, M. A.

2017-12-01

Melt extraction from the Earth's mantle through high-porosity channels is required to explain the composition of the oceanic crust. Feedbacks from reactive melt transport are thought to localize melt into a network of high-porosity channels. Recent studies invoke lithological heterogeneities in the Earth's mantle to seed the localization of partial melts. Therefore, it is necessary to understand the reaction fronts that form as melt flows across the lithological interface of a heterogeneity and the background mantle. Simplified melting models of such systems aide in the interpretation and formulation of larger scale mantle models. Motivated by the aforementioned facts, we present a chromatographic analysis of reactive melt transport across lithological boundaries, using theory for hyperbolic conservation laws. This is an extension of well-known linear trace element chromatography to the coupling of major elements and energy transport. Our analysis allows the prediction of the feedbacks that arise in reactive melt transport due to melting, freezing, dissolution and precipitation for frontal reactions. This study considers the simplified case of a rigid, partially molten porous medium with binary solid solution. As melt traverses a lithological contact-modeled as a Riemann problem-a rich set of features arise, including a reacted zone between an advancing reaction front and partial chemical preservation of the initial contact. Reactive instabilities observed in this study originate at the lithological interface rather than along a chemical gradient as in most studies of mantle dynamics. We present a regime diagram that predicts where reaction fronts become unstable, thereby allowing melt localization into high-porosity channels through reactive instabilities. After constructing the regime diagram, we test the one-dimensional hyperbolic theory against two-dimensional numerical experiments. The one-dimensional hyperbolic theory is sufficient for predicting the qualitative behavior of reactive melt transport simulations conducted in two-dimensions. The theoretical framework presented can be extended to more complex and realistic phase behavior, and is therefore a useful tool for understanding nonlinear feedbacks in reactive melt transport problems relevant to mantle dynamics.

Re-Os isotope and platinum group elements of a FOcal ZOne mantle source, Louisville Seamounts Chain, Pacific ocean

NASA Astrophysics Data System (ADS)

Tejada, Maria Luisa G.; Hanyu, Takeshi; Ishikawa, Akira; Senda, Ryoko; Suzuki, Katsuhiko; Fitton, Godfrey; Williams, Rebecca

2015-02-01

The Louisville Seamount Chain (LSC) is, besides the Hawaiian-Emperor Chain, one of the longest-lived hotspot traces. We report here the first Re-Os isotope and platinum group element (PGE) data for Canopus, Rigil, and Burton Guyots along the chain, which were drilled during IODP Expedition 330. The LSC basalts possess (187Os/188Os)i = 0.1245-0.1314 that are remarkably homogeneous and do not vary with age. A Re-Os isochron age of 64.9 ± 3.2 Ma was obtained for Burton seamount (the youngest of the three seamounts drilled), consistent with 40Ar-39Ar data. Isochron-derived initial 187Os/188Os ratio of 0.1272 ± 0.0008, together with data for olivines (0.1271-0.1275), are within the estimated primitive mantle values. This (187Os/188Os)i range is similar to those of Rarotonga (0.124-0.139) and Samoan shield (0.1276-0.1313) basalts and lower than those of Cook-Austral (0.136-0.155) and Hawaiian shield (0.1283-0.1578) basalts, suggesting little or no recycled component in the LSC mantle source. The PGE data of LSC basalts are distinct from those of oceanic lower crust. Variation in PGE patterns can be largely explained by different low degrees of melting under sulfide-saturated conditions of the same relatively fertile mantle source, consistent with their primitive mantle-like Os and primordial Ne isotope signatures. The PGE patterns and the low 187Os/188Os composition of LSC basalts contrast with those of Ontong Java Plateau (OJP) tholeiites. We conclude that the Re-Os isotope and PGE composition of LSC basalts reflect a relatively pure deep-sourced common mantle sampled by some ocean island basalts but is not discernible in the composition of OJP tholeiites.

A Sharp Continent-Ocean Transition in the Area of the Canary Islands: Evidence From Upper Mantle and Lower Crustal Xenoliths

NASA Astrophysics Data System (ADS)

Neumann, E.; Vannucci, R.; Tiepolo, M.; Griffin, W. L.; Pearson, N. J.; O'Reilly, S. Y.

2005-05-01

Our present information on passive margins rests almost exclusively on seismic and density data. An important exception is the west Iberia margin where petrological and geochemical information on crustal and mantle rocks have been made available through drilling experiments. In order to increase our information about, and understanding of, passive margins and their mode of formation, more information on crustal and mantle rocks along different types of passive margins are needed. In the area of the Canary Islands such information has been obtained through the study of mantle and deep crustal xenoliths brought to the surface by basaltic magmas. In-situ laser ablation (LA) ICP-MS mineral analyses have enabled us to "see through" the effects of the Canary Islands event and obtain robust information about the original (pre-Canarian) chemical character of the crust and upper mantle on which these islands are built. Our studies show that the lithosphere beneath the Canary Islands originated as highly refractory N-MORB type oceanic mantle overlain by highly refractory N-MORB crust. Both the lithospheric mantle and lower crust have been metasomatized to different degrees by a variety of fluid and melts. The enriched material is commonly concentrated along grain boundaries and cracks through mineral grains, suggesting that the metasomatism is relatively recent, and is thus associated with the Canary Islands magmatism. The original, strongly depleted trace element patterns and the low 87Sr/86Sr isotopic ratios typical of the oceanic lithosphere are preserved in the minerals in the least metasomatized rocks (e.g. LaN/LuN<0.1 in orthopyroxene and 87Sr/86Sr=0.7027-0.7029 in clinopyroxene in mantle xenoliths). The compositions of the most depleted gabbro samples from the different islands are closely similar, implying that there was no significant change in chemistry during the early stages of formation of the Atlantic oceanic crust in this area. Strongly depleted gabbros similar to those collected in Fuerteventura have also been retrieved in the MARK area along the central Mid-Atlantic Ridge. Furthermore, we have found no evidence of continental material that might reflect attenuated continental lithosphere in this area. The easternmost Canary Islands, Fuerteventura and Lanzarote, appear to overlap the lower part of the continental slope of Africa. The presence of normal oceanic lithosphere beneath these islands implies that the continent-ocean transition in the Canary Islands area must be relatively sharp, in contrast to the passive non-volcanic margin further north along the coast of Morocco, along the Iberia peninsula, and in many other areas. Our data also contradict the hypothesis that a mantle plume was present in this area during the opening of the Atlantic Ocean.

Record of Cyclical Massive Upwellings from the Pacific Large Low Shear Velocity Province in the Mesozoic

NASA Astrophysics Data System (ADS)

Gazel, E.; Madrigal, P.; Flores, K. E.; Bizimis, M.; Jicha, B. R.

2016-12-01

Global tomography and numerical models suggest that mantle plume occurrences are closely linked to the margins of the large low shear velocity provinces (LLSVPs). In these locations the ascent of material from the core-mantle boundary connects the deep Earth with surface processes through mantle plume activity, forming large igneous provinces (LIPs) and some of the modern hotspot volcanoes. Petrological and geodynamic evidence suggest a link between the formation of oceanic plateaus and the interactions of mantle plumes and mid-ocean ridges (MOR). Therefore, it is possible to trace the potential interactions between MORs and deep mantle plume upwellings by referencing the tectonic and magmatic evolution of the Pacific Plate in time to the current location of the LLSVP, considering the long-lived ( 500 Ma) existence of these thermochemical anomalies. We identified episodic upwellings of the Pacific LLSVP during the Mesozoic separated by 10 to 20 Ma, by reconstructing the kinematic evolution of the Pacific Plate in the last 170 Ma. The fact that the bulk emplacement of LIPs ( 120-80 Ma) in the Pacific coincides with the timing of the Cretaceous Normal Superchron, that can be related to fluctuations of mantle-core heat fluxes further supports the hypothesis of deep mantle origin for LIPs. The potential cyclicity of LIP emplacement could be tied to core heat fluctuations interacting with the lower mantle, the rheology contrast of material crossing the transition zone (either upwelling hot material or downgoing dense slabs as mantle avalanches), the rate of entrainment of recycled materials, or a combination of the processes mentioned. Recognizing patterns and possible cycles is crucial to the link between deep processes and life as these pulses impacted the marine biota resulting in episodes of anoxia and mass extinctions shortly after their eruption.

Blood Levels of Trace Elements in Children with Attention-Deficit Hyperactivity Disorder: Results from a Case-Control Study.

PubMed

Yang, Rongwang; Zhang, Yanyi; Gao, Weijia; Lin, Nannan; Li, Rong; Zhao, Zhengyan

2018-06-16

Some trace elements may participate in the pathogenesis of attention-deficit hyperactivity disorder (ADHD). This study aimed to investigate the trace element status of zinc (Zn), copper (Cu), iron (Fe), magnesium (Mg), and lead (Pb) in children with ADHD, and to compare them with normal controls. Associations between examined elements and SNAP-IV rating scores of ADHD symptoms were also assessed. Four hundred nineteen children with ADHD (8.8 ± 2.1 years) and 395 matched normal controls (8.9 ± 1.7 years) were recruited in the study. The concentrations of Zn, Fe, Cu, Mg, and Pb in the whole blood were measured by atomic absorption spectrometry. Lower zinc levels (P < 0.001) and the number out of normal ranges (P = 0.015) were found in children with ADHD when compared with the normal control group. The difference remained when adjusting the factor of BMI z-score. No significant between-group differences were found in levels of other elements. Zinc levels were negatively correlated with parent-rated scores of inattentive subscale of SNAP-IV (r = - 0.40) as well as with total score of SNAP-IV (r = - 0.24). Other significant associations were not observed. The present results indicated that there were alterations in blood levels of zinc, which was associated with the symptom scores of ADHD.

Highly Siderophile Elements in Pallasites and Diogenites, Including the New Pallasite, CMS 04071

NASA Technical Reports Server (NTRS)

Danielson, L. R.; Humayun, M.; Righter, K.

2006-01-01

Pallasites are long thought to represent a metallic core-silicate mantle boundary, where the IIIAB irons are linked to the crystallization history of the metallic fraction, and the HED meteorites may be linked to the silicate fraction. However, measurement of trace elements in individual metallic and silicate phases is necessary in order to fully under-stand the petrogenetic history of pallasites, as well as any magmatic processes which may link pallasites to both IIIAB irons and HED meteorites. In order to achieve this objective, abundances of a suite of elements were measured, including the highly siderophile elements (HSEs), in kamacite, taenite, troilite, schreibersite, chromite and olivine for the pallasites Admire, Imilac, Springwater, CMS 04071. In the diogenites GRO 95555, LAP 91900, and MET 00436, metal, sulfide, spinel, pyroxene, and silica were individually measured.

The Origin of Basalt and Cause of Melting Beneath East Antarctica as Revealed by the Southernmost Volcanoes on Earth

NASA Astrophysics Data System (ADS)

Reindel, J. L.; Panter, K. S.; Smellie, J. L.; McIntosh, W. C.

2017-12-01

Mt. Early and Sheridan Bluff are two basaltic monogenetic volcanoes located at 87° South latitude at the head of the Scott Glacier. These Early Miocene volcanoes lie 800 km from any other volcano and 200 km inland from the shoulder of the West Antarctic Rift System (WARS), which is the foci of most Cenozoic alkaline volcanism in Antarctica. Preliminary 40Ar/39Ar dates suggest that Mt. Early is older than previously determined and closer in age to Sheridan Bluff ( 19 Ma). Petrography, mineral chemistry and whole rock major and trace element concentrations are used to characterize the basalts and to determine whether they are genetically related to mafic volcanism in the WARS. The basalts are porphyritic with phenocrysts of olivine (Fo 58-84%), plagioclase (An 48-67%) ± clinopyroxene (Wo 43-48%). Whole rock MgO range from 10 to 4 wt.% and have restricted SiO2 (48 to 50 wt.%) contents. The basalts vary from alkaline (up to 6 wt.% Ne-normative) to subalkaline (up to 6 wt.% Hy-normative). The alkaline basalts that occur at both Mt. Early and Sheridan Bluff are more strongly enriched in incompatible elements (La 33-49 ppm, Ba 270-484 ppm, Sr 712-1009 ppm), have LaN/YbN ratios >10 and show prominent Pb negative anomalies with only slight K negative anomalies on primitive mantle normalized, multi-element diagrams. Subalkaline basalts (only at Sheridan Bluff) have lower concentrations of incompatible elements (La 14-16 ppm, Ba 110-144 ppm, and Sr 358-380 ppm), LaN/YbN ratios <5, and lack Pb and K negative anomalies but show minor P negative anomalies. The generation of both alkaline and subalkaline basalts is likely controlled by changes in the degree of partial melting of a compositionally similar mantle source. However, it is difficult to explain what caused the change since it would have to occur suddenly to account for the coexistence of both compositional types at Sheridan Bluff. Extension related to the WARS may be the cause, however, an alternative mechanism that could trigger melting is lithospheric delamination. The removal of old and cold mantle lithosphere from the base of the East Antarctic craton and its replacement by warmer asthenosphere has been proposed for this region based on geophysical evidence (Heeszel et al., 2016). The volcanism may constrain the timing of this event. Heeszel et al. (2016) JGR, 121, 1758-1775.

Effect of silicon on activity coefficients of siderophile elements (Au, Pd, Pt, P, Ga, Cu, Zn, and Pb) in liquid Fe: Roles of core formation, late sulfide matte, and late veneer in shaping terrestrial mantle geochemistry

NASA Astrophysics Data System (ADS)

Righter, K.; Pando, K.; Humayun, M.; Waeselmann, N.; Yang, S.; Boujibar, A.; Danielson, L. R.

2018-07-01

Earth's core contains ∼10% of a light element that may be a combination of Si, S, C, O or H, with Si potentially being the major light element. Metal-silicate partitioning of siderophile elements can place important constraints on the P-T-fO2 and composition of the early Earth, but the effect of Si alloyed in Fe liquids is unknown for many of these elements. In particular, the effect of Si on the partitioning of highly siderophile elements (Au, Re and PGE) is virtually unknown. To address this gap in understanding, we have undertaken a systematic study of the highly siderophile elements Au, Pd, and Pt, and the volatile siderophile elements P, Ga, Cu, Zn, and Pb at variable Si content of metal, and 1600 °C and 1 GPa. From our experiments we derive epsilon interaction parameters between these elements and Si in Fe metallic liquids. The new parameters are used to update an activity model for trace siderophile elements in Fe alloys; Si causes large variation in the magnitude of activity coefficients of these elements in FeSi liquids. Because the interaction parameters are all positive, Si causes a decrease in their metal/silicate partition coefficients. We combine these new activity results with experimental studies of Au, Pd, Pt, P, Ga, Cu, Zn and Pb, to derive predictive expressions for metal/silicate partition coefficients which can then be applied to Earth. The expressions are applied to two scenarios for continuous accretion of Earth; specifically for constant and increasing fO2 during accretion. The results indicate that mantle concentrations of P, Ga, Cu, Zn, and Pb can be explained by metal-silicate equilibrium during accretion of the Earth where Earth's early magma ocean deepens to pressures of 40-60 GPa. Au, Pd, and Pt, on the other hand become too high in the mantle in such a scenario, and require a later removal mechanism, rather than an addition as traditionally argued. A late reduction event that removes 0.5% metal from a shallow magma ocean can lower the Au, Pd, and Pt contents to values near the current day BSE. On the other hand, removal of 0.2-1.0% of a late sulfide-rich matte to the core would lower the Au, Pd, and Pt concentrations in the mantle, but not to chondritic relative concentrations observed in the BSE. If sulfide matte is called upon to remove HSEs, they must be later added via a late veneer to re-establish the high and chondritic relative PUM concentrations. These results suggest that although accretion and core formation (involving a Si, S, and C-bearing metallic liquid) were the primary processes establishing many of Earth's mantle volatile elements and HSE, a secondary removal process is required to establish HSEs at their current and near-chondritic relative BSE levels. Mn and P - two siderophile elements that are central to biochemical processes (photosynthesis and triphosphates, respectively) - have significant and opposite interactions with FeSi liquids, and their mantle concentrations would be notably different if Earth had a Si-free core.

Metal concentrations in the mussel Bathymodiolus platifrons from a cold seep in the South China Sea

NASA Astrophysics Data System (ADS)

Wang, Xiaocheng; Li, Chaolun; Zhou, Li

2017-11-01

Data regarding the concentration and distribution of various metals in different tissues of mussels from the cold seep is scant. We aimed to quantify the presence of twenty elements (Ca, K, Mg, Sr, Ag, Al, As, Ba, Cd, Co, Cr, Cu, Li, Fe, Mn, Mo, Ni, Pb, V, and Zn) in gills, mantles and shells of Bathymodiolus platifrons, a common mussel species in deep-sea cold seep and hydrothermal vent communities. Specimens of B. platifrons were sampled from a cold seep at the northern continental slope of the South China Sea and the elemental contents in its tissues were quantified. Our findings were compared to data from taxonomically similar species at hydrothermal vents and coastal waters. We found that most elements were significantly enriched in the gills, which could be related to food uptake and the existence of endosymbionts. In shells and mantles, Mn was particularly rich, possibly due to its replacement of Ca in the carbonate structure. A significant positive correlation among Ca, Sr, and Mg was found in both gills and mantles, consistent with relationships observed in vent and littoral mussel species. Concentrations of metals were highest in the new-growth outer edges of shells in comparison to older shell material, which suggests that trace metals have become more abundant in the ambient seawater in recent years. Compared with other deep-sea environments and coastal areas, metal accumulation showed local variability but similar overall patterns of uptake and accumulation, indicating that essential elemental requirements in different mussel species may be similar across taxa. The high bioconcentration factor (BCF) values of Mn and Ag suggest that their particular functions and regulation mechanisms are related to specific adaptations and life cycle processes.

The Chemical Structure of the Hawaiian Mantle Plume

NASA Astrophysics Data System (ADS)

Ren, Z.; Hirano, N.; Hirata, T.; Takahashi, E.; Ingle, S.

2004-12-01

Numerous geochemical studies of Hawaiian basaltic lavas have shown that the Hawaiian mantle plume is isotopically heterogeneous. However, the distribution and scale of these heterogeneities remain unknown. This is essentially due to the complex interactions created by melting a heterogeneous source, subsequent aggregation of the melts on their way to the surface, and mixing that takes place in shallow magma chambers prior to eruption. In sum, the measured compositions of bulk lavas may represent only _eaverage_f compositions that do not fully reflect the complexity of either the mantle source heterogeneity and/or chemical structure. Melt inclusions, or samples of the local magma frozen in olivine phenocrysts during their formation, are better at recording the complex magmatic history than are the bulk samples. Here, we report major and trace element compositions of olivine-hosted melt inclusions from submarine Haleakala lavas that were collected by 2001-2002 JAMSTEC cruises measured by EPMA and LA-ICP-MS after homogenization at 1250° C, QFM for 20min. Melt inclusions from the submarine Hana Ridge (Haleakala volcano) show large ranges in CaO/Al2O3 (0.92-1.50), TiO2/Na2O (0.79-1.60) and Sr/Nb (14.56-36.60), Zr/Nb (6.48-16.95), ranging from Kilauea-like to Mauna Loa-like compositions within separately-sampled lavas as well as in a single host lava sample. Bulk rocks geochemistry shows that major element composition and trace element ratios such as Zr/Nb, Sr/Nb (Ren et al., 2004a, in press, J. Petrol.) together with Pb, Nd and Sr isotopic ratios (Ren et al., 2004b, submitted to J. Petrol.) of Haleakala shield volcano also display systematic compositional variation changing from a Kilauea-like in the submarine Hana Ridge (main shield stage) to Kilauea-Mauna Loa-like in the subaerial Honomanu stage (late shield stage, data from Chen and Frey, 1991). Some of the compositional variations in melt inclusions in single rocks are wider range than over-all variation observed in bulk rocks. It is important that both Kilauea-like and Mauna Loa-like compositions co-exist in melt inclusions in single submarine Hana Ridge rocks which are identified as Kilauea-like based on bulk geochemistry. These observations are inconsistent with the current interpretation that magma compositions are controlled by concentric zonation of the Hawaiian mantle plume (e.g. Kea component and Loa component), manifested as the Kea trend and the Loa trend volcanoes (e.g. Hauri, 1996; Lassiter et al., 1996). Our new data from olivine-hosted melt inclusions imply that the chemical structure of the Hawaiian mantle plume is significantly more complicated than previously modeled and the length-scale of chemical heterogeneity must be remarkably smaller than estimated based on bulk rock geochemistry.

Early Archean sialic crust of the Siberian craton: Its composition and origin of magmatic protoliths

NASA Astrophysics Data System (ADS)

Vovna, G. M.; Mishkin, M. A.; Sakhno, V. G.; Zarubina, N. V.

2009-12-01

This study demonstrates that the base of the Archean deep-seated granulite complexes within the Siberian craton consists of a metabasite-enderbite association. The major and trace element distribution patterns revealed that the protoliths of this association are represented by calc-alkaline andesites and dacites, containing several minor sequences of komatiitic-tholeiitic volcanic rocks. The origin of the primary volcanic rocks of the metabasite-enderbite association is inferred on the basis of a model of mantle plume magmatism, which postulates that both andesitic and dacitic melts were derived from the primary basitic crust at the expense of heat generated by ascending mantle plumes. The formation of the protoliths of the Archen metabasite-enderbite association of the Siberian craton began at 3.4 Ga and continued until the late Archean.

The carbonatite-marble dykes of Abyan Province, Yemen Republic: the mixing of mantle and crustal carbonate materials revealed by isotope and trace element analysis

NASA Astrophysics Data System (ADS)

Le Bas, M. J.; Ba-Bttat, M. A. O.; Taylor, R. N.; Milton, J. A.; Windley, B. F.; Evins, P. M.

2004-09-01

Dykes of carbonate rocks, that cut gneisses in the Lowder-Mudiah area of southern Yemen, consist of dolomite and/or calcite with or without apatite, barite and monazite. Petrographic observations, mineralogical, XRF and ICP-MS analyses reveal that some of the carbonate rocks are derived from sedimentary protoliths, whereas others are magmatic calcio- and magnesio-carbonatites some of which are mineralized with barite-monazite. The interbanded occurrence and apparent contemporary emplacement of these different rock types within individual dykes, backed by Sr Nd isotope evidence, are interpreted to show that intrusion of mantle-derived carbonatite magma was accompanied by mobilization of crustal marbles. That took place some 840 Ma ago but the REE-mineralization is dated at ca. 400 Ma.

OIB signatures in basin-related lithosphere-derived alkaline basalts from the Batain basin (Oman) - Constraints from 40Ar/39Ar ages and Nd-Sr-Pb-Hf isotopes

NASA Astrophysics Data System (ADS)

Witte, M.; Jung, S.; Pfänder, J. A.; Romer, R. L.; Mayer, B.; Garbe-Schönberg, D.

2017-08-01

Tertiary rift-related intraplate basanites from the Batain basin of northeastern Oman have low SiO2 (< 45.6 wt.%), high MgO (> 9.73 wt.%) and moderate to high Cr and Ni contents (Cr > 261 ppm, Ni > 181 ppm), representing near primary magmas that have undergone fractionation of mainly olivine and magnetite. Rare earth element systematics and p-T estimates suggest that the alkaline rocks are generated by different degrees of partial melting (4-13%) of a spinel-peridotite lithospheric mantle containing residual amphibole. The alkaline rocks show restricted variations of 87Sr/86Sr and 143Nd/144Nd ranging from 0.70340 to 0.70405 and 0.51275 to 0.51284, respectively. Variations in Pb isotopes (206Pb/204Pb: 18.59-18.82, 207Pb/204Pb: 15.54-15.56, 208Pb/204Pb: 38.65-38.98) of the alkaline rocks fall in the range of most OIB. Trace element constraints together with Sr-Nd-Pb isotope composition indicate that assimilation through crustal material did not affect the lavas. Instead, trace element variations can be explained by melting of a lithospheric mantle source that was metasomatized by an OIB-type magma that was accumulated at the base of the lithosphere sometimes in the past. Although only an area of less than 1000 km2 was sampled, magmatic activity lasted for about 5.5 Ma with a virtually continuous activity from 40.7 ± 0.7 to 35.3 ± 0.6 Ma. During this period magma composition was nearly constant, i.e. the degree of melting and the nature of the tapped source did not change significantly over time.

Imaging the Lowermost Mantle (D'') Beneath the Pacific Ocean with SKKS coda waves

NASA Astrophysics Data System (ADS)

Yu, Z.; Shang, X.; van der Hilst, R. D.

2013-12-01

Previous studies indicate considerable complexity in the lowermost mantle beneath the Pacific Ocean on a variety of spatial scales, such as large low-shear-velocity province (LLSVP), intermittent D'' discontinuities and isolated ultra-low-velocity zones (ULVZs). However, the resolution of travel time tomography is typically greater than 1000 km in deep mantle, and only a few regions can satisfy contingent sampling requirement for waveform modeling. On the other hand, generalized Radon transform (GRT) has a higher resolution (~400 km horizontally and ~30 km vertically) and can relax the restriction of source-receiver configuration. It has been successfully applied to central America and east Asia, which are speculated as the graveyard of subducted slabs. In this study we apply GRT to obtain a large-scale high-resolution image beneath (almost the whole) Pacific Ocean near the core-mantle boundary (CMB). More than 400,000 traces from ~8,000 events (5.8

Effect of hereditary haemochromatosis genotypes and iron overload on other trace elements.

PubMed

Beckett, Jeffrey M; Ball, Madeleine J

2013-02-01

Hereditary haemochromatosis is a common genetic disorder involving dysregulation of iron absorption. There is some evidence to suggest that abnormal iron absorption and metabolism may influence the status of other important trace elements. In this study, the effect of abnormal HFE genotypes and associated iron overload on the status of other trace elements was examined. Dietary data and blood samples were collected from 199 subjects (mean age = 55.4 years; range = 21-81 years). Dietary intakes, serum selenium, copper and zinc concentrations and related antioxidant enzymes (glutathione peroxidase and superoxide dismutase) in subjects with normal HFE genotype (n = 118) were compared to those with abnormal HFE genotype, with both normal iron status (n = 42) and iron overload (n = 39). For most dietary and biochemical variables measured, there were no significant differences between study groups. Red cell GPx was significantly higher in male subjects with normal genotypes and normal iron status compared to those with abnormal genotypes and normal iron status (P = 0.03) or iron overload (P = 0.001). Red cell GPx was also highest in normal women and significantly lower in the abnormal genotype and normal iron group (P = 0.016), but not in the iron overload group (P = 0.078). Although it may not be possible to exclude a small effect between the genotype groups on RBC GPx, overall, haemochromatosis genotypes or iron overload did not appear to have a significant effect on selenium, copper or zinc status.

Why Does Some Subducted Continental Crust Escape Deformation and Transformation?

NASA Astrophysics Data System (ADS)

Garber, J. M.; Kylander-Clark, A. R.; Stearns, M.; Seward, G.; Hacker, B. R.

2016-12-01

Titanite geochemistry and geochronology from the Western Gneiss Region (WGR) of Norway shows that large portions of continental crust were deeply subducted and exhumed without significantly deforming or transforming, indicating heterogeneous mechanical behavior of crust at mantle depths. Titanite is stable in granitic rocks over a significant P-T range, and contains numerous major, minor, and trace elements that record 1) P-T conditions, 2) interactions with other major and accessory phases, and 3) information about the composition of coeval melts and fluids. A large titanite LA-ICP-MS dataset from WGR granitic gneisses and leucosomes yields a record that depends strongly on textural setting: some titanites formed after the decomposition of other phases at mantle depths, but other titanites preserve inherited isotopic dates and chemistry with variable recrystallization at grain rims. Differences in rock textures, as well as changes in volatile abundances (F and OH) among different titanite populations, suggest that the persistence of crustal minerals at mantle depths is coupled with limited prograde fluid infiltration, which restricted the efficacy of metamorphic reactions, likely increased rock strength, and caused heterogeneities in the density of the subducting slab. The observed expanses of untransformed, undeformed granitic crust may have been critical to coupling the continental crust to underlying mantle lithosphere, which prevented significant internal deformation of the slab (e.g,. Young et al., 2007; Butler et al., 2015). Finally, our statistical approach shows the utility of dimensional reduction in geochemical studies: rather than comparing individual element or isotopic abundances or ratios, principal components or discriminant analyses can condense variables and help efficiently distinguish between distinct geologic agents or geochemical reservoirs.

Boron Isotope Evidence for Shallow Fluid Transfer Across Subduction Zones by Serpentinized Mantle

NASA Astrophysics Data System (ADS)

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

2012-12-01

Boron Isotope Evidence for Shallow Fluid Transfer Across Subduction Zones by Serpentinized Mantle M. Scambelluri (1), S. Tonarini (2), S. Agostini (2), E. Cannaò (1) (1) Dipartimento di Scienze della Terra, Ambiente e vita, University of Genova, Italy (2) Istituto di Geoscienze e Georisorse-CNR, Pisa, Italy In subduction zones, fluid-mediated chemical exchange between slabs and mantle dictates volatile and incompatible element cycles and influences arc magmatism. Outstanding issues concern the sources of water for arc magmas and its slab-to-mantle wedge transport. Does it occur by slab dehydration beneath arc fronts, or by hydration of fore-arc mantle and subsequent subduction of the hydrated mantle? So far, the deep slab dehydration hypothesis had strong support, but the hydrated mantle wedge idea is advancing supported by studies of fluid-mobile elements in serpentinized wedge peridotites and their subducted high-pressure (HP) equivalents. Serpentinites are volatile and fluid-mobile element reservoirs for subduction: their dehydration causes large fluid and element flux to the mantle.However, direct evidence for their key role in arc magmatism and identification of dehydration environments has been elusive and boron isotopes can trace the process. Until recently, the altered oceanic crust (AOC) was considered the 11B reservoir for arcs, which largely display positive δ11B. However, shallow slab dehydration transfers 11B to the fore-arc mantle and leaves the residual AOC very depleted in 11B below arcs. Here we present high positive δ11B of HP serpentinized peridotites from Erro Tobbio (Ligurian Alps), recording subduction metamorphism from hydration at low-grade to eclogite-facies dehydration. We show a connection among serpentinite dehydration, release of 11B-rich fluids and arc magmatism. The dataset is completed by B isotope data on other HP Alpine serpentinites from Liguria and Lanzo Massif. In general, the δ11B of these rocks is heavy (16 to + 30 permil). No significant B loss and 11B fractionation occurs with burial. Their B and 11B abundance shows that high budgets acquired during shallow hydration are transferred to HP fluids, providing the heavy-boron component requested for arcs. The B compositions of Erro-Tobbio are unexpected for slabs, deputed to loose B and 11B during dehydration: its isotopic composition can be achieved diluting in the mantle shallow subduction-fluids (30 km). The serpentinizing fluids and the fluid-transfer mechanism in Erro-Tobbio are clarified integrating B with O-H and Sr isotopes. Low δD (-102permil), high δ18O (8permil) of early serpentinites suggest low-temperature hydration by metamorphic fluids. 87Sr/86Sr (0.7044 to 0.7065) is lower than oceanic serpentinites formed from seawater. We conclude that alteration was distant from mid-ocean ridges and occurred at the slab-mantle interface or in forearc environments. We thus provide evidence for delivery of water and 11B at sub-arcs by serpentinized mantle altered by subduction-fluid infiltration atop of the slab since the early stages of burial, witnessing shallow fluid transfer across the subduction zone. Similarity of the B composition of Erro Tobbio with other Alpine serpentinized peridotites suggests that these materials might have spent much of their subduction lifetime at the plate interface, fed by B and 11Bich fluids uprising from the slab.

New Experimental Constraints on Crystallization Differentiation in a Deep Magma Ocean

NASA Astrophysics Data System (ADS)

Walter, M. J.; Ito, E.; Nakamura, E.; Tronnes, R.; Frost, D.

2001-12-01

Most of Earth's mass probably accreted as a consequence of numerous impacts between large bodies and proto-Earth, and a giant impact with a Mars-sized object is the most plausible explanation for a Moon forming event. 1 Physical models show that large impacts would have caused high-degrees of melting and a global magma ocean. 2 Crystallization differentiation in a deep magma ocean could impart stratification in the solidified mantle, forming large geochemical domains. To accurately model crystallization in a deep magma ocean the liquidus phase-relations of peridotite, as well as mineral/melt element partitioning, must be known at lower mantle conditions. Here, we report the results of liquidus experiments on fertile model peridotite compositions at 23 - 33 GPa. Experiments were performed in 6/8-type multi-anvil apparatus using carbide and sintered-diamond second-stage anvils with 4 and 2 mm truncations, respectively. Samples were encapsulated by either graphite or Re. High-temperatures were generated using LaCrO3 or Re furnaces, and temperatures were held from 2 to 50 minutes at 2300 - 2500 C. Run products were analyzed for major and trace elements using EPMA and SIMS. At 23 GPa the liquidus phase is majorite, followed closely down temperature by ferropericlase (Fp) and Mg-perovskite (Mg-Pv). At 24 GPa the liquidus phase has changed to Fp, followed closely by majorite and Mg-Pv. Ca-perovskite (Ca-Pv) is present only at much lower temperatures close to the solidus. At approximately 31 GPa Mg-Pv is the liquidus phase followed down-temperature by Fp then Ca-Pv. At ~ 33 GPa Ca-Pv crystallizes closer to the liquidus, within about 50 C, at a similar temperature to Fp. Thus, important phases crystallizing in a deep magma ocean are Mg-Pv, Ca-Pv and Fp. Crystallization models based on major element partitioning show that only very modest amounts of crystal separation of a Mg-Pv + Fp assemblage can be tolerated before Ca/Al, Al/Ti and Ca/Ti ratios become unrealistic for estimates of primitive upper mantle (PUM). 3 However, even small amounts of Ca-Pv in the crystal assemblage effectively buffer these ratios at values close to the starting composition (e.g. chondritic). Further, based on our new trace element partitioning data, models involving considerable Mg-Pv fractionation generally show poor matches with model PUM. For example, model PUM has sub-chondritic REE/Ti, whereas these ratios increase considerably during Mg-Pv crystallization. Notable exceptions are super-chondritic Zr/Ti, chondritic Sr/Ti, and sub-chondritic Zr/Nb and Sm/Yb ratios, all of which are well matched by considerable Mg-Pv crystallization. Although trace element D's for Ca-Pv are not yet measured quantitatively, the observed affinity of Ca-Pv for REE could conceivably account for the the sub-chondritic REE/Ti ratios in PUM. Ca-Pv also concentrates K, and could be an important source of heat from radioactive decay in the lower mantle. 1. Canup, R. and Agnor, C., Origin of the Earth and Moon, Righter and Canup, eds., U. Arizona Press, 113-144, 2000. 2. Melosh, H., Origin of the Earth, Newsom and Jones, eds., Oxford Press, 69-84, 1990. 3. McFarlane, E. et al., Geochimica et Cosmochimica Acta, 5161-5172, 1994.

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.

Mantle Plumes and Geologically Recent Volcanism on Mars

NASA Astrophysics Data System (ADS)

Kiefer, W. S.

2013-12-01

Despite its small size, Mars has remained volcanically active until the geologically recent past. Crater retention ages on the volcanos Arsia Mon, Olympus Mons, and Pavonis Mons indicate significant volcanic activity in the last 100-200 million years. The radiometric ages of many shergottites, a type of igneous martian meteorite, indicate igneous activity at about 180 million years ago. These ages correspond to the most recent 2-4% of the age of the Solar System. The most likely explanation for this young martian volcanism is adiabatic decompression melting in upwelling mantle plumes. Multiple plumes may be active at any time, with each of the major volcanos in the Tharsis region being formed by a separate plume. Like at least some terrestrial mantle plumes, mantle plumes on Mars likely form via an instability of the thermal boundary layer at the base of the mantle. Because Mars operates in the stagnant lid convection regime, the temperature difference between mantle and core is lower than on Earth. This reduces the temperature contrast between mantle and core, resulting in mantle plumes on Mars that are about 100 K hotter than the average mantle. The chemical composition of the martian meteorites indicates that the martian mantle is enriched in both iron and sodium relative to Earth's mantle. This lowers the dry solidus on early Mars by 30-40 K relative to Earth. Migration of sodium to the crust over time decreases this difference in solidus temperature to about 15 K at present, but that is sufficient to increase the current plume magma production rate by a factor of about 2. Hydrous phases in the martian meteorites indicate the presence of a few hundred ppm water in the mantle source region, roughly the same as Earth. Finite element simulations of martian plumes using temperature-dependent viscosity and realistic Rayleigh numbers can reproduce the geologically recent magma production rate that is inferred from geologic mapping and the melt fraction inferred from trace element studies of martian meteorites. These plumes can also reproduce the observed spatial variability in elastic lithosphere thickness between regions of plume upwelling and regions that are far from the plumes. Melting in these models occurs at pressures of 3-5 GPa (250-400 km depth), reflecting the presence of a thick thermal lithosphere on present-day Mars. Meteorite evidence indicates that the martian mantle has about 10 times as much isotopic heterogeneity as Earth, which has sometimes been interpreted as evidence that the martian mantle is not convecting. This conclusion is incorrect, as the observed volcanos require some form of decompression melting and thus a convecting mantle. Few strike slip faults are observed on Mars, which indicates that flow in the mantle is almost entirely poloidal in nature, with little or no toroidal motion. The absence of toroidal flow on Mars makes convective mixing much less efficient than on Earth and permits the preservation of high levels of isotopic heterogeneity within a convecting mantle.

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).

Timing and composition of continental volcanism at Harrat Hutaymah, western Saudi Arabia

USGS Publications Warehouse

Duncan, Robert A.; Kent, Adam J R; Thornber, Carl; Schliedler, Tyler D; Al-Amri, Abdullah M

2016-01-01

Harrat Hutaymah is an alkali basalt volcanic field in north-central Saudi Arabia, at the eastern margin of a large Neogene continental, intraplate magmatic province. Lava flow, tephra and spatter cone compositions in the field include alkali olivine basalts and basanites. These compositions contrast with the predominantly tholeiitic, fissure-fed basalts found along the eastern margin of the Red Sea. The Hutaymah lava flows were erupted through Proterozoic arc-associated plutonic and meta-sedimentary rocks of the Arabian shield, and commonly contain a range of sub-continental lithospheric xenoliths, although the lavas themselves show little indication of crustal contamination. Previous radiometric dating of this volcanic field (a single published K–Ar age; 1.8 Ma) is suspiciously old given the field measurement of normal magnetic polarity only (i.e. Brunhes interval, ≤ 780 Ka). We report new age determinations on 14 lava flows by the 40Ar–39Ar laser step heating method, all younger than ~ 850 Ka, to better constrain the time frame of volcanism, and major, trace and rare earth element compositions to describe the chemical variation of volcanic activity at Harrat Hutaymah. Crystal fractionation was dominated by olivine ± clinopyroxene at a range of upper mantle and crustal pressures. Rapid ascent and eruption of magma is indicated by the array of lower crustal and lithospheric xenoliths observed in lava flows and tephra. Modeling suggests 1–7% melting of an enriched asthenospheric mantle source occurred beneath Harrat Hutaymah under a relatively thick lithospheric cap (60–80 km).

Petrogenesis of the Majiari ophiolite (western Tibet, China): Implications for intra-oceanic subduction in the Bangong-Nujiang Tethys

NASA Astrophysics Data System (ADS)

Huang, Qiang-tai; Liu, Wei-liang; Xia, Bin; Cai, Zhou-rong; Chen, Wei-yan; Li, Jian-feng; Yin, Zheng-xin

2017-09-01

The Majiari ophiolite lies in the western Bangong-Nujiang Suture Zone, which separates the Qiangtang and Lhasa blocks in central Tibet. The ophiolite consists of peridotite, gabbro/diabase and basalt. Zircon U-Pb dating yielded an age of 170.5 ± 1.7 Ma for the gabbro, whereas 40Ar/39Ar dating of plagioclase from the same gabbro yielded ages of 108.4 ± 2.6 Ma (plateau age) and 112 ± 2 Ma (isochron age), indicating that the ophiolite was formed during the Middle Jurassic and was probably emplaced during the Early Cretaceous. Zircons from the gabbro have εHf(t) values ranging from +6.9 to +10.6 and f(Lu/Hf) values ranging from -0.92 to -0.98. Mafic lavas plot in the tholeiitic basalt field but are depleted in Nb, Ta and Ti and enriched in Rb, Ba and Th in the N-MORB-normalized trace element spider diagram. These lavas have whole-rock εNd(t) values of +5.9 to +6.6, suggesting that they were derived from a depleted mantle source, which was probably modified by subducted materials. The Majiari ophiolite probably formed in a typical back-arc basin above a supra-subduction zone (SSZ) mantle wedge. Intra-oceanic subduction occurred during the Middle Jurassic and collision of the Lhasa and South Qiangtang terranes likely occurred in the Early Cretaceous. Thus, closure of the Bangong-Nujiang Tethys Ocean likely occurred before the Early Cretaceous.

Timing and composition of continental volcanism at Harrat Hutaymah, western Saudi Arabia

NASA Astrophysics Data System (ADS)

Duncan, Robert A.; Kent, Adam J. R.; Thornber, Carl R.; Schlieder, Tyler D.; Al-Amri, Abdullah M.

2016-03-01

Harrat Hutaymah is an alkali basalt volcanic field in north-central Saudi Arabia, at the eastern margin of a large Neogene continental, intraplate magmatic province. Lava flow, tephra and spatter cone compositions in the field include alkali olivine basalts and basanites. These compositions contrast with the predominantly tholeiitic, fissure-fed basalts found along the eastern margin of the Red Sea. The Hutaymah lava flows were erupted through Proterozoic arc-associated plutonic and meta-sedimentary rocks of the Arabian shield, and commonly contain a range of sub-continental lithospheric xenoliths, although the lavas themselves show little indication of crustal contamination. Previous radiometric dating of this volcanic field (a single published K-Ar age; 1.8 Ma) is suspiciously old given the field measurement of normal magnetic polarity only (i.e. Brunhes interval, ≤ 780 Ka). We report new age determinations on 14 lava flows by the 40Ar-39Ar laser step heating method, all younger than ~ 850 Ka, to better constrain the time frame of volcanism, and major, trace and rare earth element compositions to describe the chemical variation of volcanic activity at Harrat Hutaymah. Crystal fractionation was dominated by olivine ± clinopyroxene at a range of upper mantle and crustal pressures. Rapid ascent and eruption of magma is indicated by the array of lower crustal and lithospheric xenoliths observed in lava flows and tephra. Modeling suggests 1-7% melting of an enriched asthenospheric mantle source occurred beneath Harrat Hutaymah under a relatively thick lithospheric cap (60-80 km).

Trace element concentrations in the fruit peels and trunks of Musa paradisiaca.

PubMed

Selema, M D; Farago, M E

1996-08-01

Chemical analyses for the elementary compositions of the ashes of the fruit peels and trunks of the tropical plantain Musa paradisiaca have been undertaken. The elements, categorized as trace elements, generally are found to have higher mean concentrations in the fruit peels than in the trunks (except in the case of Zn). Their peel-trunk uptake ratios have been calculated and range between 1 and 4, showing normal levels of accumulations in the fruit peels over the trunks.

186Os-187Os and highly siderophile element abundance systematics of the mantle revealed by abyssal peridotites and Os-rich alloys

NASA Astrophysics Data System (ADS)

Day, James M. D.; Walker, Richard J.; Warren, Jessica M.

2017-03-01

Abyssal peridotites are oceanic mantle fragments that were recently processed through ridges and represent residues of both modern and ancient melting. To constrain the nature and timing of melt depletion processes, and the composition of the mantle, we report high-precision Os isotope data for abyssal peridotites from three ocean basins, as well as for Os-rich alloys, primarily from Mesozoic ophiolites. These data are complemented by whole-rock highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, Re), trace- and major-element abundances for the abyssal peridotites, which are from the Southwest Indian (SWIR), Central Indian (CIR), Mid-Atlantic (MAR) and Gakkel Ridges. The results reveal a limited role for melt refertilization or secondary alteration processes in modifying abyssal peridotite HSE compositions. The abyssal peridotites examined have experienced variable melt depletion (2% to >16%), which occurred >0.5 Ga ago for some samples. Abyssal peridotites typically exhibit low Pd/Ir and, combined with high-degrees of estimated total melt extraction, imply that they were relatively refractory residues prior to incorporation into their present ridge setting. Recent partial melting processes and mid-ocean ridge basalt (MORB) generation therefore played a limited role in the chemical evolution of their precursor mantle domains. The results confirm that many abyssal peridotites are not simple residues of recent MORB source melting, having a more complex and long-lived depletion history. Peridotites from the Gakkel Ridge, SWIR, CIR and MAR indicate that the depleted MORB mantle has 186Os/188Os of 0.1198356 ± 21 (2SD). The Phanerozoic Os-rich alloys yield an average 186Os/188Os within uncertainty of abyssal peridotites (0.1198361 ± 20). Melt depletion trends defined between Os isotopes and melt extraction indices (e.g., Al2O3) allow an estimate of the primitive mantle (PM) composition, using only abyssal peridotites. This yields 187Os/188Os (0.1292 ± 25), and 186Os/188Os of 0.1198388 ± 29, both of which are within uncertainty of previous primitive mantle estimates. The 186Os/188Os composition of the PM is less radiogenic than for some plume-related lavas, with the latter requiring sources with high long-term time-integrated Pt/Os. Estimates of primitive mantle HSE concentrations using abyssal peridotites define chondritic Pd/Ir, which differs from previous supra-chondritic estimates for Pd/Ir based on peridotites from a range of tectonic settings. By contrast, estimates of PM yield supra-chondritic Ru/Ir. The cause of enhanced Ru in the mantle remains enigmatic, but may reflect variable partitioning behavior of Ru at high pressure and temperature.

Alkaline magmatism in the Amambay area, NE Paraguay: The Cerro Sarambí complex

NASA Astrophysics Data System (ADS)

Gomes, C. B.; Velázquez, V. F.; Azzone, R. G.; Paula, G. S.

2011-07-01

The Early Cretaceous alkaline magmatism in the northeastern region of Paraguay (Amambay Province) is represented by stocks, plugs, dikes, and dike swarms emplaced into Carboniferous to Triassic-Jurassic sediments and Precambrian rocks. This magmatism is tectonically related to the Ponta Porã Arch, a NE-trending structural feature, and has the Cerro Sarambí and Cerro Chiriguelo carbonatite complexes as its most significant expressions. Other alkaline occurrences found in the area are the Cerro Guazú and the small bodies of Cerro Apuá, Arroyo Gasory, Cerro Jhú, Cerro Tayay, and Cerro Teyú. The alkaline rocks comprise ultramafic-mafic, syenitic, and carbonatitic petrographic associations in addition to lithologies of variable composition and texture occurring as dikes; fenites are described in both carbonatite complexes. Alkali feldspar and clinopyroxene, ranging from diopside to aegirine, are the most abundant minerals, with feldspathoids (nepheline, analcime), biotite, and subordinate Ti-rich garnet; minor constituents are Fe-Ti oxides and cancrinite as the main alteration product from nepheline. Chemically, the Amambay silicate rocks are potassic to highly potassic and have miaskitic affinity, with the non-cumulate intrusive types concentrated mainly in the saturated to undersaturated areas in silica syenitic fields. Fine-grained rocks are also of syenitic affiliation or represent more mafic varieties. The carbonatitic rocks consist dominantly of calciocarbonatites. Variation diagrams plotting major and trace elements vs. SiO 2 concentration for the Cerro Sarambí rocks show positive correlations for Al 2O 3, K 2O, and Rb, and negative ones for TiO 2, MgO, Fe 2O 3, CaO, P 2O 5, and Sr, indicating that fractional crystallization played an important role in the formation of the complex. Incompatible elements normalized to primitive mantle display positive spikes for Rb, La, Pb, Sr, and Sm, and negative for Nb-Ta, P, and Ti, as these negative anomalies are considerably more pronounced in the carbonatites. Chondrite-normalized REE patterns point to the high concentration of these elements and to the strong LRE/HRE fractionation. The Amambay rocks are highly enriched in radiogenic Sr and have TDM model ages that vary from 1.6 to 1.1 Ga, suggesting a mantle source enriched in incompatible elements by metasomatic events in Paleo-Mesoproterozoic times. Data are consistent with the derivation of the Cerro Sarambí rocks from a parental magma of lamprophyric (minette) composition and suggest an origin by liquid immiscibility processes for the carbonatites.

The effect of H2O and CO2 on planetary mantles

NASA Technical Reports Server (NTRS)

Wyllie, P. J.

1978-01-01

The peridotite-H2O-CO2 system is discussed, and it is shown that even traces of H2O and CO2, in minerals or vapor, lower mantle solidus temperatures through hundreds of degrees in comparison with the volatile-free solidus. The solidus for peridotite-H2O-CO2 is a divariant surface traversed by univariant lines that locate the intersections of subsolidus divariant surfaces for carbonation or hydration reactions occurring in the presence of H2O-CO2 mixtures. Vapor phase compositions are normally buffered to these lines, and near the buffered curve for the solidus of partly carbonated peridotite there is a temperature maximum on the peridotite-vapor solidus. Characteristics on the CO2 side of the maximum and on the H2O side of the maximum are described.

Trace elements in sera from patients with renal disease

NASA Astrophysics Data System (ADS)

Miura, Yoshinori; Nakai, Keiko; Sera, Kouichiro; Sato, Michirou

1999-04-01

In hemodialysis (HD) patients, an accumulation of trace elements such as aluminum, copper, silicon and vanadium has been reported. Aluminum-caused encephalopathy and aluminum-related bone diseases are important trace element-related complications. Using particle induced X-ray emission (PIXE) we determined concentrations of aluminum, silicon, copper, zinc, selenium and bromine in sera of 29 patients with HD, 14 nondialysis patients with renal disease (RD) and 27 normal controls. The concentration of serum silicon of the patients with HD was 107.4 ± 61.3 μmol/l, which is markedly higher than that of normal controls (48.3 ± 25.8 μmol/l, p < 0.0001). The serum concentrations of zinc and bromine in patients with HD were 11.9 ± 1.7 and 21.3 ± 3.0 μmol/l, respectively. Both were markedly lower than those of normal controls (15.6 ± 2.6, 69.2 ± 8.3 μmol/l, p < 0.0001). The concentrations of aluminium and bromine in the serum of patients with RD were 171.9 ± 64.3 and 81.9 ± 11.6 μmol/l, which were markedly higher than those of normal controls ( p < 0.0001, p < 0.001). No significant differences were observed in the concentration of copper and selenium among three groups.

Lithospheric heterogeneity beneath the EARS interpreted from major and trace element analyses of mafic rocks

NASA Astrophysics Data System (ADS)

Hamblock, J.; Anthony, E.; Omenda, P.; Chesley, J.

2003-04-01

We report chemical analyses for tholeiites from the axial region of the EARS and tholeiites and basanites from the Chyulu Hills Volcanic Province (CHVP), located on the SE flank of the Kenya Rift. The purpose of the study is to: i) explore contrasts in lithospheric composition from the axial region, where seismic velocities imply high temperatures and presence of melt at shallow depths, to the flanks, where geophysical studies indicate thick lithosphere and a zone of partial melt centered under the CHVP (Ritter and Kaspar, 1997, Tectonophysics 278, 149-169). ii) investigate plume components and plume-lithosphere interactions in the different settings. This study complements the characterization of lithosphere along the axis of the Rift by MacDonald et al. (2001, J. Petrol. 42, 877-900) and the study of temporal evolution of the CHVP by Späth et al. (2001, J. Petrol. 42, 765-787). Basanites within the CHVP are similar to OIB in their trace-element patterns, but with a pronounced negative K-anomaly. Späth et al. attribute this anomaly to melting of a lithospheric mantle source containing amphibole. They postulate, based on radiogenic isotopes (Sr, Pb, Nd), recent metasomatism due to interaction of the lithosphere with the EARS plume. High La/Yb suggests a source within the garnet-peridotite field. Tholeiites from the CHVP are distinct in trace-element chemistry from basanites, with flatter multi-element patterns and generally lower elemental concentrations. The CHVP tholeiites have La/Yb indicative of a spinel peridotite source. The role of crustal contamination for tholeiites remains open; however, substantial evidence exists for lithospheric heterogeneity beneath the CHVP. Axial lavas show similar elemental behavior as the CHVP: basanites have negative K-anomalies (MacDonald et al., 2001), whereas tholeiites do not. Tholeiites have flat multi-element patterns with low overall concentrations, similar to those from the CHVP, with one significant difference tholeiites from the axial region have variable and high concentrations of Ba, K, and Ta, which may represent a more pervasive plume component. The Mg-number of lavas from the axial region are significantly lower than lavas in the CHVP, suggesting greater degrees of crystal fractionation and potentially longer residence times in crustal magma chambers. In conclusion, evidence exists in both areas for lithospheric mantle heterogeneity, but in both areas the elemental signature is highly correlated to silica saturation. For a given group of lavas of similar silica saturation, the elemental patterns are similar from the axis to the flank. This observation implies that there are not strong lateral contrasts in lithospheric composition across the EARS.

Generation of Silicic Melts in the Early Izu-Bonin Arc Recorded by Detrital Zircons in Proximal Arc Volcaniclastic Rocks From the Philippine Sea

NASA Astrophysics Data System (ADS)

Barth, A. P.; Tani, K.; Meffre, S.; Wooden, J. L.; Coble, M. A.; Arculus, R. J.; Ishizuka, O.; Shukle, J. T.

2017-10-01

A 1.2 km thick Paleogene volcaniclastic section at International Ocean Discovery Program Site 351-U1438 preserves the deep-marine, proximal record of Izu-Bonin oceanic arc initiation, and volcano evolution along the Kyushu-Palau Ridge (KPR). Pb/U ages and trace element compositions of zircons recovered from volcaniclastic sandstones preserve a remarkable temporal record of juvenile island arc evolution. Pb/U ages ranging from 43 to 27 Ma are compatible with provenance in one or more active arc edifices of the northern KPR. The abundances of selected trace elements with high concentrations provide insight into the genesis of U1438 detrital zircon host melts, and represent useful indicators of both short and long-term variations in melt compositions in arc settings. The Site U1438 zircons span the compositional range between zircons from mid-ocean ridge gabbros and zircons from relatively enriched continental arcs, as predicted for melts in a primitive oceanic arc setting derived from a highly depleted mantle source. Melt zircon saturation temperatures and Ti-in-zircon thermometry suggest a provenance in relatively cool and silicic melts that evolved toward more Th and U-rich compositions with time. Th, U, and light rare earth element enrichments beginning about 35 Ma are consistent with detrital zircons recording development of regional arc asymmetry and selective trace element-enriched rear arc silicic melts as the juvenile Izu-Bonin arc evolved.

Geochemical fingerprints of Late Triassic calc-alkaline lamprophyres from the Eastern Pontides, NE Turkey: A key to understanding lamprophyre formation in a subduction-related environment

NASA Astrophysics Data System (ADS)

Karsli, Orhan; Dokuz, Abdurrahman; Kaliwoda, Melanie; Uysal, Ibrahim; Aydin, Faruk; Kandemir, Raif; Fehr, Karl-Thomas

2014-05-01

The Eastern Pontides in NE Turkey is one of the major orogenic belts in Anatolia. In this paper, we report our new 40Ar/39Ar dating, mineral chemistry, major and trace elements and Sr-Nd-Pb isotopic analyses of the lamprophyre intrusions in this region. The lamprophyres are widely scattered and intrude Late Carboniferous granitoid rocks. The lamprophyres exhibit fine-grained textures and are mineralogically uniform. Hornblende 40Ar/39Ar dating yielded a plateau age of 216.01 ± 10.64 Ma. Based on their geochemistry, mineral compositions and paragenesis, the lamprophyres are classified as calc-alkaline lamprophyres in general and spessartites in particular, which are rich in large ion lithophile elements (e.g., Rb, Ba, K) but depleted in Nb and Ti. Our samples exhibit moderate fractionation in LREE patterns approximately 100 times that of chondrite but HREE abundances less than 10 times that of chondrite. These calc-alkaline lamprophyres display a range of ISr (216 Ma) values from 0.70619 to 0.71291 and ɛNd (216 Ma) values from - 1.4 to 4.1, with TDM = 1.11 to 2.20 Ga. Their Pb isotopic ratios indicate an enriched mantle source. The enrichment process is related to metasomatism of a subcontinental lithospheric mantle source, which is caused by a large quantity of H2O-rich fluids, rather than sediments released from oceanic crust at depth during the closure of the Paleotethys Ocean in Triassic times. All of the geochemical data and the trace element modeling suggest that the primary magma of the calc-alkaline to high-K calc-alkaline spessartites was generated at depth by a low degree of partial melting (~ 1-10%) of a previously enriched lithospheric mantle wedge consisting of phlogopite-bearing spinel peridotite. The ascendance of a hot asthenosphere triggered by extensional events caused partial melting of mantle material. The rising melts were accompanied by fractional crystallization and crustal contamination en route to the surface. All of the geochemical features combined with regional data suggest that the Eastern Pontides calc-alkaline lamprophyres originated in an extensional environment along an active continental margin throughout the Late Triassic. Such an extensional event, causing upwelling of hot asthenosphere, led to the opening of the northern branch of the Neotethys as a back-arc basin farther south of the Eastern Pontides.

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.

Apollo 15 yellow-brown volcanic glass - Chemistry and petrogenetic relations to green volcanic glass and olivine-normative mare basalts

NASA Technical Reports Server (NTRS)

Hughes, S. S.; Schmitt, R. A.; Delano, J. W.

1988-01-01

Electron microprobe and INAA were used to analyze forty spherules of Apollo 15 yellow-brown glass for major and trace elements. The glass is one of twenty-five high-Mg primary magmas emplaced on the lunar surface in pyroclastic eruptions. The abundances show that the magma was produced by partial melting of differentiated cumulates in the lunar mantle. Models to explain the possible source-regions of several Apollo 15 and Apollo 12 low-Ti mare magmas are presented.

Noble metal abundances in komatiite suites from Alexo, Ontario and Gorgona Island, Colombia

NASA Astrophysics Data System (ADS)

Brügmann, G. E.; Arndt, N. T.; Hofmann, A. W.; Tobschall, H. J.

1987-08-01

The distribution of the chalcophile and siderophile metals Cu, Ni, Au, Pd, Ir, Os and Ru in an Archaean komatiite flow from Alexo, Ontario and in a Phanerozoic komatiitic suite of Gorgona Island, Colombia, provides new information about the geochemical behaviour of these elements. Copper, Au and Pd behave as incompatible elements during the crystallization of these ultramafic magmas. In contrast, Ni, Ir, Os and Ru concentrations systematically decrease with decreasing MgO contents, a pattern characteristic of compatible elements. These trends are most probably controlled by olivine crystallization, which implies that Ir, Os and Ru are compatible in olivine. Calculated partition coefficients for Ir, Os and Ru between olivine and the melt are about 1.8. Compared to primitive mantle, parental komatiitic liquids are enriched in (incompatible) Cu, Au and Pd and depleted in (compatible) Ir, Os and Ru. Within both Archaean and Phanerozoic komatiites, noble metal ratios such as Au/Pd, Ir/Os, Os/Ru and Ru/Ir and ratios of lithophile and siderophile elements such as Ti/Pd, Ti/Au are constant and similar to primitive mantle values. This implies that Au and Pd are moderately incompatible elements and that there has been no significant fractionation of siderophile and lithophile elements since the Archaean. Platinum-group element abundances of normal MORB are highly variable and always much lower than in komatiites, because MORB magma is saturated with sulfur and a variable but minor amount of sulfide segregated during mantle melting or during the ascent of magma to the surface. Sulfide deposits associated with komatiites display similar chalcophile element patterns to those of komatiites. Noble metal ratios such as Pd/Ir, Au/Ir, Pd/Os and Pd/Ru can be used to determine the composition of the host komatiite at the time of sulfide segregation.

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.

The effect of tissue structure and soil chemistry on trace element uptake in fossils

NASA Astrophysics Data System (ADS)

Hinz, Emily A.; Kohn, Matthew J.

2010-06-01

Trace element profiles for common divalent cations (Sr, Zn, Ba), rare-earth elements (REE), Y, U, and Th were measured in fossil bones and teeth from the c. 25 ka Merrell locality, Montana, USA, by using laser-ablation ICP-MS. Multiple traverses in teeth were transformed into 2-D trace element maps for visualizing structural influences on trace element uptake. Trace element compositions of different soils from the fossil site were also analyzed by solution ICP-MS, employing progressive leaches that included distilled H 2O, 0.1 M acetic acid, and microwave digestion in concentrated HCl-HNO 3. In teeth, trace element uptake in enamel is 2-4 orders of magnitude slower than in dentine, forming an effective trace element barrier. Uptake in dentine parallel to the dentine-enamel interface is enhanced by at least 2 orders of magnitude compared to transverse, causing trace element "plumes" down the tooth core. In bone, U, Ba and Sr are nearly homogeneous, implying diffusivities ˜5 orders of magnitude faster than in enamel and virtually complete equilibration with host soils. In contrast all REE show strong depletions inward, with stepwise linear segments in log-normal or inverse complementary error function plots; these data require a multi-medium diffusion model, with about 2 orders of magnitude difference in slowest vs. fastest diffusivities. Differences in REE diffusivities in bone (slow) vs. dentine (fast) reflect different partition coefficients ( Kd's). Although acid leaches and bulk digestion of soils yield comparable fossil-soil Kd's among different elements, natural solutions are expected to be neutral to slightly basic. Distilled H 2O leachates instead reveal radically different Kd's in bone for REE than for U-Sr-Ba, suggest orders of magnitude lower effective diffusivities for REE, and readily explain steep vs. flat profiles for REE vs. U-Sr-Ba, respectively. Differences among REE Kd's and diffusivities may explain inward changes in Ce anomalies. Acid washes and bulk soil compositions yield misleading Kd's for many trace elements, especially the REE, and H 2O-leaches are preferred. Patterns of trace element distributions indicate diagenetic alteration at all scales, including enamel, and challenge the use of trace elements in paleodietary studies.

Mantle hydrous-fluid interaction with Archaean granite.

NASA Astrophysics Data System (ADS)

Słaby, E.; Martin, H.; Hamada, M.; Śmigielski, M.; Domonik, A.; Götze, J.; Hoefs, J.; Hałas, S.; Simon, K.; Devidal, J.-L.; Moyen, J.-F.; Jayananda, M.

2012-04-01

Water content/species in alkali feldspars from late Archaean Closepet igneous bodies as well as growth and re-growth textures, trace element and oxygen isotope composition have been studied (Słaby et al., 2011). Both processes growth and re-growth are deterministic, however they differ showing increasing persistency in element behaviour during interaction with fluids. The re-growth process fertilized domains and didn't change their oxygen-isotope signature. Water speciation showed persistent behaviour during heating at least up to 600oC. Carbonate crystals with mantle isotope signature are associated with the recrystallized feldspar domains. Fluid-affected domains in apatite provide evidence of halide exchange. The data testify that the observed recrystallization was a high-temperature reaction with fertilized, halide-rich H2O-CO2 mantle-derived fluids of high water activity. A wet mantle being able to generate hydrous plumes, which appear to be hotter during the Archean in comparison to the present time is supposed by Shimizu et al. (2001). Usually hot fluids, which can be strongly carbonic, precede asthenospheric mantle upwelling. They are supposed to be parental to most recognized compositions, which can be derived by their immiscible separation into saline aqueous-silicic and carbonatitic members (Klein-BenDavid et al., 2007). The aqueous fractions are halogen-rich with a significant proportion of CO2. Both admixed fractions are supposed to be fertile. The Closepet granite emplaced in a major shear zone that delimitates two different terrains. Generally such shear zones, at many places, are supposed to be rooted deep into the mantle. The drain, that favoured and controlled magma ascent and emplacement, seemed to remain efficient after granite crystallization. In the southern part of the Closepet batholiths an evidence of intensive interaction of a lower crust fluid (of high CO2 activity) is provided by the extensive charnockitization of amphibolite facies (Stähle et al., 1987).The previously published data as well as the new ones point to volatile elements from both mantle and crust playing a prominent role in the petrogenesis of magmatic rocks during the Archaean. Their composition differs significantly in regard to water and CO2 activity. The present contribution gives an evidence of hydrous mantle-derived fluids. Taking under consideration two-end members model proposed for Archaean mantle, the contribution favours wet-mantle model. The work has been done within the framework of IGCP-SIDA 599 and has been funded by IGSci PASci 'Hybrid' and IGSci PASci-CNRS-UMR 6524-LMV project: 'Equilibration and re-equilibration processes in Archaean granites'. Klein-BenDavid, O., Izraeli, E.S., Hauri, E. & Navon, O. (2007). Fluid inclusions in diamonds from the Diavik mine, Canada and the evolution of diamond-forming fluids. Geochimica et Cosmochimica Acta 71, 723-744. Słaby, E., Martin, H., Hamada, M., Śmigielski, M., Domonik, A., Götze, J., Hoefs, J., Hałas, S., Simon, K., Devidal, J-L., Moyen, J-F., Jayananda, M. (2011) Evidence in Archaean alkali-feldspar megacrysts for high-temperature interaction with mantle fluids. Journal of Petrology (on line). doi:10.1093/petrology/egr056. Stähle, H.J., Raith, M., Hoernes, S. & Delfs, A. (1987). Element mobility during incipient granulite formation at Kabbaldurga, Southern India. Journal of Petrology 28, 803-834.

Dietary exposure estimates of twenty-one trace elements from a Total Diet Study carried out in Pavia, Northern Italy.

PubMed

Turconi, Giovanna; Minoia, Claudio; Ronchi, Anna; Roggi, Carla

2009-04-01

The significant role of trace elements in human health is well documented. Trace elements are those compounds that need to be present in the human diet to maintain normal physiological functions. However, some microelements may become harmful at high levels of exposure, or, on the other hand, may give rise to malnutrition, when their exposure is too low. The aim of the present study was to provide a reliable estimate of the dietary exposure of twenty-one trace elements in a Northern Italian area. For this purpose, trace element analyses were undertaken on total diet samples collected from a university cafeteria in Pavia, Northern Italy. The average daily exposure for the adult people was calculated on the basis of food consumption frequency, portion size and trace element levels in foodstuffs. The mean exposure values satisfy the Italian RDA for all the essential trace elements, except for Fe exposure in females, and are well below the Provisional Tolerable Daily Intake for all the toxic compounds, showing that the probability of dietary exposure to health risks is overall small. As far as Fe exposure is concerned, a potential risk of anaemia in the female adult population should be considered, then studies aimed at evaluating the Fe nutritional status of adult Italian women should be addressed. In conclusion, while not excluding the possibility that the daily exposure determined in the present study may not be representative of the population as a whole, this study provides a good estimate of the Italian adult consumer exposure to twenty-one trace elements.

Geochemical and isotopic (Nd-Pb-Sr-O) variations bearing on the genesis of volcanic rocks from Vesuvius, Italy

USGS Publications Warehouse

Ayuso, R.A.; de Vivo, B.; Rolandi, G.; Seal, R.R.; Paone, A.

1998-01-01

Alkaline volcanism produced by Monte Somma-Vesuvius volcano includes explosive plinian and subplinian activity in addition to effusive lava flows. Pumice, scoria, and lava (150 samples) exhibit major- and trace-element gradients as a function of SiO2 (58.9-47.2 wt%) and MgO (0-7.8 wt%); Mg value are ???50. Internally gradational chemical groups or cycles are distinguished by age: (1) 25 000 to 14 000 yr B.P.; (2) 8000 yr B.P. to A.D. 79; and (3) A.D. 79 to 1944. A small number of lavas, dikes and scora were also analysed from the Somma formation (~ 35 000 to 25 000 yr B.P.). Within each group, contents of Na2O + K2O increas with decreasing MgO along distinct rocks. Nb/Y values are variable from 0.66 to 3.14 (at SiO2 ??? 50 wt%) generally in the range of alkaline and ultra-alkaline rocks. Variations in contents of some majro elements (e.g., P and Ti), and trace elements (e.g., Th, Nb, Ta, Zr, Hf, Pb, La, and Sc), as well as contrasting trends in ratios of various elements (e.g., Ta/Yb, Hf/U, Th/Ta, Th/Hf, Th/Yb, etc.) are also generally consistent with the group subdivisions. For example, Th/Hf increases from ??? 5 to ??? 10 with decreasing age for the Vesuvius system as a whole, yielding similar compositions in the least evolved rocks (low-silica, high-MgO, imcompatible element-poor) erupted at the end of each cycle. Internal variations within individual eruptions also systematically changed generally towards a common mafic composition at the end of each cycle, thus reflecting the dominanit volume in the magma chamber. At the start of a new eruptive cycle, the rocks are relatively enriched in incompatible elements; younger groups also contain higher abundances than other groups. N-MORB-normalized multielement diagrams exhibit selective enrichments of Sr, K, Rb, Th, and the light rare-earth elements; deep Nb and Ta negative anomalies commonly seen in rocks generated at orogenic margins are absent in the light rare-earth elements; deep Nb and Ta netgative anomalies commonly seen in rocks generated at orogenic margins are absent in our samples. Sr isotopic compositions are known to be variable within some of the units, in agreement with our data (87Sr/86Sr ~ 0.70699 to 0.70803) and with contributions from several isotopic components. Isotopic compositions for ??18O (7.3 to 10.2%), Pb for mineral separates and whole rocks (206Pb/204Pb ~ 18.947 to 19.178, 207Pb/204/Pb ~ 15.617 to 15.769, 208Pb/204Pb ~38.915 to 39.345), and Nd (143Nd ~ 0.51228 to 0.51251) also show variability. Oxygen isotope data show that pumices have higher ??18O values than cogenetic lavas, and that ??18O values and SiO2 are correlated. Radiogenic and stable isotope data plot within range of isotopic compositions for the Roman comagmatic province. Fractional crystallization cannot account for the radiogenic isotopic compositions of the Vesuvius magmas. We favor instead the combined effects of heterogeneous magma sources, together with isotopic exchange near the roof of the magma chamber. We suggest that metasomatized continental mantle lithosphere is the principal source of the magmas. This kind of enriched mantle was melted and reactivated in an area of continental extension (incipient rift setting) without direct reliance on contemporaneous subduction processes but possibly with input from mantle sources that resemble those that produce ocean island basalts.

Different origins of garnet in high pressure to ultrahigh pressure metamorphic rocks

NASA Astrophysics Data System (ADS)

Xia, Qiong-Xia; Zhou, Li-Gang

2017-09-01

Garnet in high-pressure (HP) to ultrahigh-pressure (UHP) metamorphic rocks in subduction zone commonly shows considerable zonation in major and trace elements as well as mineral inclusions, which bears information on its growth mechanism via metamorphic or peritectic reactions in coexistence with relic minerals and metamorphic fluids or anatectic melts at subduction-zone conditions. It provides an important target to retrieve physicochemical changes in subduction-zone processes, including those not only in pressure and temperature but also in the durations of metamorphism and anatexis. Garnet from different compositions of HP to UHP metamorphic rocks may show different types of major and trace element zonation, as well as mineral inclusions. Discrimination between the different origins of garnet provides important constraints on pressure and temperature and the evolution history for the HP to UHP metamorphic rocks. Magmatic garnet may occur as relics in granitic gneisses despite metamorphic modification at subduction-zone conditions, with spessartine-increasing or flat major element profiles from inner to outer core and exceptionally higher contents of trace elements than metamorphic mantle and rim. Metamorphic garnet can grow at different metamorphic stages during prograde subduction and retrograde exhumation, with spessartine-decreasing from core to rim if the intracrystalline diffusion is not too fast. The compositional profiles of metamorphic garnet in the abundances of grossular, almandine and pyrope are variable depending on the composition of host rocks and co-existing minerals. Peritectic garnet grows through peritectic reactions during partial melting of HP to UHP rocks, with the composition of major elements to be controlled by anatectic P-T conditions and the compositions of parental rocks and anatectic melts. Trace element profiles in garnet with different origins are also variable depending on the coexisting mineral assemblages, the garnet-forming reactions and the property of metamorphic fluids or anatectic melts. Mineral inclusions not only present key clues to identify the different origins of garnet, but also serve as sound candidates for the temporal constraint on garnet growth.

Petrology and geochemistry of the Tasse mantle xenoliths of the Canadian Cordillera: A record of Archean to Quaternary mantle growth, metasomatism, removal, and melting

NASA Astrophysics Data System (ADS)

Polat, Ali; Frei, Robert; Longstaffe, Fred J.; Thorkelson, Derek J.; Friedman, Eyal

2018-07-01

Mantle xenoliths hosted by the Quaternary Tasse alkaline basalts in the Canadian Cordillera, southeastern British Columbia, are mostly spinel lherzolite originating from subcontinental lithospheric mantle. The xenoliths contain abundant feldspar veins, melt pockets and spongy clinopyroxene, recording extensive alkaline metasomatism and partial melting. Feldspar occurs as veins and interstitial crystal in melt pockets. Melt pockets occur mainly at triple junctions, along grain boundaries, and consist mainly of olivine, cpx, opx and spinel surrounded by interstitial feldspar. The Nd, Sr and Pb isotopic compositions of the xenoliths indicate that their sources are characterized by variable mixtures of depleted MORB mantle and EM1 and EM2 mantle components. Large variations in εNd values (-8.2 to +9.6) and Nd depleted mantle model ages (TDM = 66 to 3380 Ma) are consistent with multiple sources and melt extraction events, and long-term (>3300 Ma) isolation of some source regions from the convecting mantle. Samples with Archean and Paleoproterozoic Nd model ages are interpreted as either have been derived from relict Laurentian mantle pieces beneath the Cordillera or have been eroded from the root of the Laurentian craton to the east and transported to the base of the Cordilleran lithosphere by edge-driven convection currents. The oxygen isotope compositions of the xenoliths (average δ18O = +5.1 ± 0.5‰) are similar to those of depleted mantle. The average δ18O values of olivine (+5.0 ± 0.2‰), opx (+5.9 ± 0.6‰), cpx (+6.0 ± 0.6‰) and spinel (+4.5 ± 0.2‰) are similar to mantle values. Large fractionations for olivine-opx, olivine-cpx and opx-cpx pairs, however, reflect disequilibrium stemming from metasomatism and partial melting. Whole-rock trace element, Nd, Sr, Pb and O isotope compositions of the xenoliths and host alkaline basalts indicate different mantle sources for these two suites of rocks. The xenoliths were derived from shallow lithospheric sources, whereas the alkaline basalts originated from a deeper asthenospheric mantle source.

[Analysis of X-ray fluorescence spectroscopy and plasma mass spectrometry of the Guidong granite body and its implications to granite evolution].

PubMed

Li, Hong-Wei; Chen, Guo-Neng; Peng, Zhuo-Lun

2013-07-01

The Guidong composite granite body (CGB) located in the north Guangdong Province consists of numerous rock bodies formed respectively in the early and late Jurassic and early Cretaceous. Analysis of the granites of different period with X-ray fluorescence spectroscopy and plasma mass spectrometry indicates: (1) From the top of a granite body downwards, the felsic components of rock decrease, while the mafic and sigmaREE, LREE/HREE, (La/Yb)N, as well as delta Eu value increase, suggesting the material differentiation in the in-situ melting of crustal rocks and crystallisation of magma; (2) From old to young of the different period granite-massifs in the Guidong CGB, the felsic compositions totally decrease, and the mafic components, sigmaEE, LREE/HREE, (La/Yb)N, and delta Eu value increase as well, implying multiple crustal melting (remelting) events in the Mesozoic in this area; and (3) Primitive mantle-normalized spider diagram for trace elements of Guidong CGB suggests high maturity of the crust involved in the in-situ melting.

Slab melting beneath the Cascade Arc driven by dehydration of altered oceanic peridotite

NASA Astrophysics Data System (ADS)

Walowski, K. J.; Wallace, P. J.; Hauri, E. H.; Wada, I.; Clynne, M. A.

2015-05-01

Water is returned to Earth’s interior at subduction zones. However, the processes and pathways by which water leaves the subducting plate and causes melting beneath volcanic arcs are complex; the source of the water--subducting sediment, altered oceanic crust, or hydrated mantle in the downgoing plate--is debated; and the role of slab temperature is unclear. Here we analyse the hydrogen-isotope and trace-element signature of melt inclusions in ash samples from the Cascade Arc, where young, hot lithosphere subducts. Comparing these data with published analyses, we find that fluids in the Cascade magmas are sourced from deeper parts of the subducting slab--hydrated mantle peridotite in the slab interior--compared with fluids in magmas from the Marianas Arc, where older, colder lithosphere subducts. We use geodynamic modelling to show that, in the hotter subduction zone, the upper crust of the subducting slab rapidly dehydrates at shallow depths. With continued subduction, fluids released from the deeper plate interior migrate into the dehydrated parts, causing those to melt. These melts in turn migrate into the overlying mantle wedge, where they trigger further melting. Our results provide a physical model to explain melting of the subducted plate and mass transfer from the slab to the mantle beneath arcs where relatively young oceanic lithosphere is subducted.

Diverse Metals and Sulfides in Polymict Ureilites EET 83309 and EET 87720

NASA Technical Reports Server (NTRS)

Herrin, J. S.; Mittlefehldt, D. W.; Downes, H.; Humayun, M.

2007-01-01

Ureilites are a group of carbon-bearing ultramafic achondrites. The majority of samples are monomict with major and trace element compositions consistent with a restitic origin after extensive loss of basaltic melts and significant loss of their metallic component during anatexis. Monomict ureilites are thought to represent largely intact samples of the ureilite parent body (UPB) mantle. Polymict ureilites, by contrast, are fragmental breccias consisting of welded lithic clasts and isolated mineral fragments thought to be regolith that assembled after major disruption fragmented large portions of the UPB mantle. In most polymict ureilites, the majority of clasts consist of material similar to monomict ureilites gardened from the UPB mantle but other materials, both endogenic and xenogenic to the UPB are also found in polymict ureilites, including clasts texturally and compositionally similar to known chondrite types as well as feldspathic melt rocks and clasts of Ca-Al-Ti-rich assemblages. In this study, we demonstrate that polymict ureilites also contain a variety of metal and sulfide compositions of diverse origins. They offer insight into the final equilibrium conditions of disrupted portions of the UPB mantle and the diversity of materials locally available for regolith formation, and provide evidence for only limited post-regolith formation thermal metamorphism.

Slab melting beneath the Cascades Arc driven by dehydration of altered oceanic peridotite

USGS Publications Warehouse

Walowski, Kristina J; Wallace, Paul J.; Hauri, E.H.; Wada, I.; Clynne, Michael A.

2015-01-01

Water is returned to Earth’s interior at subduction zones. However, the processes and pathways by which water leaves the subducting plate and causes melting beneath volcanic arcs are complex; the source of the water—subducting sediment, altered oceanic crust, or hydrated mantle in the downgoing plate—is debated; and the role of slab temperature is unclear. Here we analyse the hydrogen-isotope and trace-element signature of melt inclusions in ash samples from the Cascade Arc, where young, hot lithosphere subducts. Comparing these data with published analyses, we find that fluids in the Cascade magmas are sourced from deeper parts of the subducting slab—hydrated mantle peridotite in the slab interior—compared with fluids in magmas from the Marianas Arc, where older, colder lithosphere subducts. We use geodynamic modelling to show that, in the hotter subduction zone, the upper crust of the subducting slab rapidly dehydrates at shallow depths. With continued subduction, fluids released from the deeper plate interior migrate into the dehydrated parts, causing those to melt. These melts in turn migrate into the overlying mantle wedge, where they trigger further melting. Our results provide a physical model to explain melting of the subducted plate and mass transfer from the slab to the mantle beneath arcs where relatively young oceanic lithosphere is subducted.

The Chemical Behavior of Fluids Released during Deep Subduction Based on Fluid Inclusions

NASA Astrophysics Data System (ADS)

Frezzotti, M. L.; Ferrando, S.

2014-12-01

We present a review of current research on fluid inclusions in (HP-) UHP metamorphic rocks that, combined with existing experimental research and thermodynamic models, allow us to investigate the chemical and physical properties of fluids released during deep subduction, their solvent and element transport capacity, and the subsequent implications for the element recycling in the mantle wedge. An impressive number of fluid inclusion studies indicate three main populations of fluid inclusions in HP and UHP metamorphic rocks: i) aqueous and/or non-polar gaseous fluid inclusions (FI), ii) multiphase solid inclusions (MSI), and iii) melt inclusions (MI). Chemical data from preserved fluid inclusions in rocks match with and implement "model" fluids by experiments and thermodynamics, revealing a continuity behind the extreme variations of physico-chemical properties of subduction-zone fluids. From fore-arc to sub-arc depths, fluids released by progressive devolatilization reactions from slab lithologies change from relatively diluted chloride-bearing aqueous solutions (± N2), mainly influenced by halide ligands, to (alkali) aluminosilicate-rich aqueous fluids, in which polymerization probably governs the solubility and transport of major (e.g., Si and Al) and trace elements (including C). Fluid inclusion data implement the petrological models explaining deep volatile liberation in subduction zones, and their flux into the mantle wedge.

Three types of element fluxes from metabasite into peridotite in analogue experiments: Insights into subduction-zone processes

NASA Astrophysics Data System (ADS)

Perchuk, A. L.; Yapaskurt, V. O.; Griffin, W. L.; Shur, M. Yu.; Gain, S. E. M.

2018-03-01

Piston-cylinder experiments with natural rocks and mineral separates were carried out at 750-900 °C and 2.9 GPa, conditions relevant to hot subduction zones, to study the mechanisms of metasomatic alteration of mantle-wedge rocks such as dunite and lherzolite, and the transfer of trace elements released from a carbonate-bearing amphibolite during its eclogitization. Element transfer from the slab to the mantle lithologies occurred in porous-, focused- and diffusive-flow regimes that remove melt and carbon, and partially water, from the metabasite layer. Porous flow is recorded by dissolution of clinopyroxene and growth of orthopyroxene ± garnet ± magnesite ± chlorite along grain boundaries in the peridotite layers, but is invisible in the metabasite layers. Porous flow of the same fluids/melts produces harzburgite mineralogy in both dunite and lherzolite. The transformation of lherzolite to harzburgite reflects breakdown of clinopyroxene in the lherzolite and diffusion of the liberated calcium into the metabasite layer, i.e. against the direction of major fluid/melt flow. Focused flow develops along the side walls of the capsules, producing a melt-free omphacite ± phengite ± quartz paragenesis in the metabasite, and melt segregations, separated from the host peridotite layers by newly-formed omphacite ± garnet ± phlogopite + orthopyroxene + magnesite. Diffusive flow leads to the formation of orthopyroxene ± magnesite ± garnet reaction zones at the metabasite-peridotite interface and some melt-peridotite interfaces. Melt segregations in the peridotite layers at 850-900 °C are rich in LREE and LILE, strongly depleted in Y and HREE, and have higher Sr/Y and La/Yb ratios than island arc andesites, dacites and rhyolites. These features, and negative anomalies in Nb-Ta and low Nb/Ta, resemble those of high-silica adakites and TTGs, but K2O is high compared to TTGs. Metasomatism in the dunite layer changes the REE patterns of dunite, recording chromatographic fractionation during porous melt flow. During metabasite-lherzolite interaction, the metabasite layer becomes mildly enriched in LREE; the lherzolite layer, in contrast, is generally depleted in LREE relative to the initial composition. This also indicates element transfer against the direction of fluid flow. Trace-element profiling reveals the development of Eu anomalies in the peridotite layers and the diffusion of many trace elements out of both layers toward the contact zone. The documented processes may be applicable to both Phanerozoic and Precambrian subduction zones.

The Nature and Origin of the ~1.88 Ga Circum-Superior Large Igneous Province

NASA Astrophysics Data System (ADS)

Minifie, M.; Kerr, A. C.; Ernst, R. E.

2009-12-01

The Circum-Superior Large Igneous Province (LIP) is composed of a discontinuous belt of magmatic rocks, predominantly mafic-ultramafic in composition, circumscribing the cratonic margins of the Superior Province in the Canadian Shield for >3000 km. In addition to the cratonic margin magmatism, magmatic rocks of the same age are found in the interior of the craton in the form of mafic-ultramafic dykes and also carbonatite complexes along the Kapuskasing Structural Zone. Recent U-Pb geochronological studies have shown a tight age grouping for these magmatic rocks between 1885 and 1864 Ma. Previous studies have treated the various segments of the Circum-Superior LIP individually and models on the origin of the magmatism include seafloor spreading, back-arc basin rifting, foredeep basin flexure, volcanic arc activity, transtension in pull-apart basins, and mantle plume activity. This study is the first to create a cohesive geochemical and Sr-Nd-Pb-Hf-Os isotopic database for the whole of the Circum-Superior LIP and to assess its petrogenesis as a single entity. The geochemical and isotopic evidence strongly favour a mantle plume origin for the Circum-Superior LIP magmatism. A common trace element signature, very much like that of the Ontong Java oceanic plateau, is persistent throughout most of this LIP. Most samples possess Zr/Y and Nb/Y ratios almost identical to Ontong Java and other oceanic plateau lavas. Utilisation of the PRIMELT2 software of Herzberg & Asimow (2008) shows that the parental magmas of the Circum-Superior LIP were derived from ~30-35% pooled fractional melting of a source composition similar to that of primitive mantle with 1% continental crust extracted from it at mantle potential temperatures ranging from 1515 to 1610° C. Basalts from islands in Hudson Bay possess slightly enriched trace element profiles with small positive Nb anomalies and highlight a degree of heterogeneity within the plume source. The Circum-Superior LIP magmatic rocks possess similar isotopic compositions which further support the notion of a common mantle source for the whole LIP. The isotopic composition of this source is distinct to that of N-MORB which precludes the role of ambient upper mantle in the petrogenesis of the Circum-Superior magmatism suggested by previous studies. Ni-Cu-PGE sulphide deposits are associated with some regions of the Circum-Superior LIP. Subtle differences in the geochemistry of the volcanic rocks in areas which are fertile with respect to Ni-Cu-PGE deposits and areas which are barren may have implications for ore prospecting in other LIPs around the world. Herzberg, C. & Asimow, P.D. 2008. Petrology of some oceanic island basalts: PRIMELT2.XLS software for primary magma calculation. Geochemistry Geophysics Geosystems 9, doi: 10.1029/2008GC002057.

Scanning transmission ion microscopy mass measurements for quantitative trace element analysis within biological samples and validation using atomic force microscopy thickness measurements

NASA Astrophysics Data System (ADS)

Devès, Guillaume; Cohen-Bouhacina, Touria; Ortega, Richard

2004-10-01

We used the nuclear microprobe techniques, micro-PIXE (particle-induced X-ray emission), micro-RBS (Rutherford backscattering spectrometry) and scanning transmission ion microscopy (STIM) in order to perform the characterization of trace element content and spatial distribution within biological samples (dehydrated cultured cells, tissues). The normalization of PIXE results was usually expressed in terms of sample dry mass as determined by micro-RBS recorded simultaneously to micro-PIXE. However, the main limit of RBS mass measurement is the sample mass loss occurring during irradiation and which could be up to 30% of the initial sample mass. We present here a new methodology for PIXE normalization and quantitative analysis of trace element within biological samples based on dry mass measurement performed by mean of STIM. The validation of STIM cell mass measurements was obtained in comparison with AFM sample thickness measurements. Results indicated the reliability of STIM mass measurement performed on biological samples and suggested that STIM should be performed for PIXE normalization. Further information deriving from direct confrontation of AFM and STIM analysis could as well be obtained, like in situ measurements of cell specific gravity within cells compartment (nucleolus and cytoplasm).

Mantle heat flow and thermal structure of the northern block of Southern Granulite Terrain, India

NASA Astrophysics Data System (ADS)

Manglik, Ajay

2006-07-01

Continental shield regions are normally characterized by low-to-moderate mantle heat flow. Archaean Dharwar craton of the Indian continental shield also follows the similar global pattern. However, some recent studies have inferred significantly higher mantle heat flow for the Proterozoic northern block of Southern Granulite Terrain (SGT) in the immediate vicinity of the Dharwar craton by assuming that the radiogenic elements depleted exposed granulites constitute the 45-km-thick crust. In this study, we use four-layered model of the crustal structure revealed by integrated geophysical studies along a geo-transect in this region to estimate the mantle heat flow. The results indicate that: (i) the mantle heat flow of the northern block of SGT is 17 ± 2 mW/m 2, supporting the global pattern, and (ii) the lateral variability of 10-12 mW/m 2 in the surface heat flow within the block is of crustal origin. In terms of temperature, the Moho beneath the eastern Salem-Namakkal region appears to be at 80-100 °C higher temperature than that beneath the western Avinashi region.

Simultaneous cryo X-ray ptychographic and fluorescence microscopy of green algae

DOE Office of Scientific and Technical Information (OSTI.GOV)

Deng, Junjing; Vine, David J.; Chen, Si

Trace metals play important roles in normal and in disease-causing biological functions. X-ray fluorescence microscopy reveals trace elements with no dependence on binding affinities (unlike with visible light fluorophores) and with improved sensitivity relative to electron probes. However, X-ray fluorescence is not very sensitive for showing the light elements that comprise the majority of cellular material. Here we show that X-ray ptychography can be combined with fluorescence to image both cellular structure and trace element distribution in frozen-hydrated cells at cryogenic temperatures, with high structural and chemical fidelity. Ptychographic reconstruction algorithms deliver phase and absorption contrast images at a resolutionmore » beyond that of the illuminating lens or beam size. Using 5.2-keV X-rays, we have obtained sub-30-nm resolution structural images and ~90-nm-resolution fluorescence images of several elements in frozen-hydrated green algae. Finally, this combined approach offers a way to study the role of trace elements in their structural context.« less

Simultaneous cryo X-ray ptychographic and fluorescence microscopy of green algae

DOE PAGES

Deng, Junjing; Vine, David J.; Chen, Si; ...

2015-02-24

Trace metals play important roles in normal and in disease-causing biological functions. X-ray fluorescence microscopy reveals trace elements with no dependence on binding affinities (unlike with visible light fluorophores) and with improved sensitivity relative to electron probes. However, X-ray fluorescence is not very sensitive for showing the light elements that comprise the majority of cellular material. Here we show that X-ray ptychography can be combined with fluorescence to image both cellular structure and trace element distribution in frozen-hydrated cells at cryogenic temperatures, with high structural and chemical fidelity. Ptychographic reconstruction algorithms deliver phase and absorption contrast images at a resolutionmore » beyond that of the illuminating lens or beam size. Using 5.2-keV X-rays, we have obtained sub-30-nm resolution structural images and ~90-nm-resolution fluorescence images of several elements in frozen-hydrated green algae. Finally, this combined approach offers a way to study the role of trace elements in their structural context.« less

Simultaneous cryo X-ray ptychographic and fluorescence microscopy of green algae

DOE Office of Scientific and Technical Information (OSTI.GOV)

Deng, Junjing; Vine, David J.; Chen, Si

Trace metals play important roles in normal and in disease-causing biological functions. X-ray fluorescence microscopy reveals trace elements with no dependence on binding affinities (unlike with visible light fluorophores) and with improved sensitivity relative to electron probes. However, X-ray fluorescence is not very sensitive for showing the light elements that comprise the majority of cellular material. Here we show that X-ray ptychography can be combined with fluorescence to image both cellular structure and trace element distribution in frozen-hydrated cells at cryogenic temperatures, with high structural and chemical fidelity. Ptychographic reconstruction algorithms deliver phase and absorption contrast images at a resolutionmore » beyond that of the illuminating lens or beam size. Using 5.2-keV X-rays, we have obtained sub-30-nm resolution structural images and similar to 90-nm-resolution fluorescence images of several elements in frozen-hydrated green algae. This combined approach offers a way to study the role of trace elements in their structural context.« less

Chapman Conference on Generation of the Oceanic Lithosphere

NASA Astrophysics Data System (ADS)

Presnall, D. C.; Hales, A. L.; Frey, F. A.

On April 6-10, 1981, the Chapman conference on Generation of the Oceanic Lithosphere was held at Airlie House, Warrenton, Virginia. It was convened by D.C. Presnall, A.L. Hales (both at the University of Texas at Dallas), and F.A. Frey (Massachusetts Institute of Technology). The purpose of the conference was to bring together scientists with diverse specialties to develop a better understanding of the constraints imposed by geophysics, geochemistry, petrology, and tectonics on processes of oceanic lithosphere generation. Sessions were held on the nature of the crust and upper mantle at spreading centers; trace elements and isotopes; experimental petrology; magma chamber dynamics, melt migration, and mantle flow; slow versus fast spreading ridges; Atlantic spreading centers; Pacific spreading centers; and hydrothermal activity, metasomatism, and metamorphism. Fifty-four oral papers and 47 poster papers were presented. One hundred twenty-eight scientists attended from Australia, Canada, Cyprus, Denmark, France, Iceland, Japan, Mexico, United Kingdom, United States, and the USSR.

Petrologic evolution of Miocene-Pliocene mafic volcanism in the Kangal and Gürün basins (Sivas-Malatya), central east Anatolia: Evidence for Miocene anorogenic magmas contaminated by continental crust

NASA Astrophysics Data System (ADS)

Kocaarslan, Ayça; Ersoy, E. Yalçın

2018-06-01

This study discusses the geochemical features of the Early-Middle Miocene and Pliocene basaltic (SiO2 = 46-52; MgO = 6-10 wt%) to andesitic (SiO2 = 59; MgO = 4 wt%) rocks exposed in the Gürün and Kangal basins (Sivas, eastern part of central Anatolia), respectively. The basaltic rocks are characterized by alkaline to tholeiitic affinities, while the more evolved andesitic samples show calc-alkaline affinity. Trace element variations reveal that they can be evaluated in three sub-groups, each represented by different contents of trace elements for given Nb contents. Primary magmas of each groups were likely produced by different degrees of partial melting ( 1-2, 2-3, 7-10% respectively) from a common mantle source, subsequently underwent different degrees of fractionation and crustal contamination. Derivation from a common mantle source of the primitive magmas of each group is supported by similar Sr, Nd and Pb isotopic ratios. Increasing degrees of partial melting seem to be responsible for the alkaline to tholeiitic variation among the basaltic samples, while higher degrees of crustal contamination (AFC) resulted in calc-alkaline affinity of the more evolved samples. Most primitive Pliocene samples show intra-plate (anorogenic) geochemical features, while the more evolved Miocene calc-alkaline samples resemble geochemically subduction-related (orogenic) magmatic rocks. However, on the basis of detailed geochemical models, we propose that the calc-alkaline affinity among the Miocene samples can also be gained by crustal contamination of their primary magmas which were also anorogenic in character. If this is true, overall, the Miocene and Pliocene basaltic to andesitic rocks in the Gürün and Kangal basins appear to may have formed by variable degrees of partial melting of a common anorogenic mantle that had not been subject to subduction-related metasomatism. This is an alternative approach to the general view assuming the Early-Middle Miocene magmatic activity in the region was derived from subduction-modified mantle sources in response to subduction of the Arabian Plate under the Anatolian Plate. This hypothesis further implies that either delamination of the sub-continental lithosphere or slab break-off processes beneath the central to eastern Anatolia might took place well before the Miocene, thus allowing upwelling unaltered mantle to provide the source of the Miocene to Pliocene volcanic rocks.

Water and metasomatism in the Slave cratonic lithosphere (Canada): an FTIR study

NASA Astrophysics Data System (ADS)

Kilgore, M.; Peslier, A. H.; Brandon, A. D.; Schaffer, L. A.; Pearson, D. G.; O'Reilly, S. Y.; Kopylova, M. G.; Griffin, W. L.

2017-12-01

Water in the mantle influences melting, viscosity, seismic velocity, and electrical conductivity. The role played by water in the long-term stabilization of cratonic roots is currently being debated [1]. This study focuses on water contents of mantle minerals (olivine, pyroxene and garnet) from xenoliths found in kimberlites of the Archean Slave craton. 19 mantle xenoliths from central Lac de Gras, and 10 from northern Jericho were analyzed by FTIR for water, and their equilibration depths span the several compositional layers identified beneath the region [2]. At both locations, the shallow peridotites have lower water contents in their olivines (11-30 ppm H2O) than those from the deeper layers (28-300 ppm H2O). The driest olivines, however, are not at the base of the cratonic lithosphere (>6 GPa) as in the Kaapvaal craton [1]. Instead, the deepest olivines are hydrous (31-72 ppm H2O at Lac de Gras and 275 ppm H2O at Jericho). Correlations of water in clinopyroxene and garnet with their other trace element contents are consistent with water being added by metasomatism by melts resembling kimberlite precursors in the mantle 0.35 Ga ago beneath Lac de Gras [1]. The northern Jericho xenoliths are derived from a region of the Slave craton that is even more chemically stratified, and was affected at depth by the 1.27 Ga Mackenzie igneous events [3,4]. Metasomatism at Jericho may be responsible for the particularly high olivine water contents (up to 300 ppm H2O) compared to those at Lac de Gras, which will be investigated by acquiring trace-element data on these xenoliths. These data indicate that several episodes of metasomatic rehydration occurred in the deep part of the Slave craton mantle lithosphere, with the process being more intense in the northern part beneath Jericho, likely related to a translithospheric suture serving as a channel to introduce fluids and/or melts in the northern region [5]. Consequently, rehydration of the lithosphere does not necessarily cause cratonic root delamination and these peridotites may represent localized metasomatic zones - the wall rocks to kimberlite magma passage. [1] Peslier et al. 2010 Nature 467, p78; [2] Aulbach et al. 2013 CG 352, p153; [3] Heaman et al. 2010 CJES 47, p369; [4] Kopylova et al. 2000 EPSL 181, p71; [5] Poudjom Djomani et al. 2005 GGG 6, n10.

Historical trace element distribution in sediments from the Mississippi River delta

USGS Publications Warehouse

Swarzenski, P.W.; Baskaran, M.; Rosenbauer, R.J.; Orem, W.H.

2006-01-01

Five sediment cores were collected on the shelf of the inner Mississippi Bight in June 2003 for a suite of radionuclides to establish geochronologies and trace elements to examine patterns of contaminant deposition and accumulation. Core sites were chosen to reflect a matrix of variable water depths, proximity to the Mississippi River mouth as the primary source for terrigenous particles, and extent and duration of summertime water column hypoxia. The vertical distribution of 239,240Pu and 210Pbxs (= 210Pbtotal - 226Ra) provided reliable geochronological age constraints to develop models for mass accumulation rates and historic trace element inputs and variations. Mass accumulation rates ranged from 0.27 to 0.87 g cm-2 yr-1 and were internally consistent using either 210Pbxs or 239,240Pu. Measured inventories of 137Cs, 239,240Pu, and 210Pbxs were compared to atmospheric deposition rates to quantify potential sediment focusing or winnowing. Observed variability in calculated mass accumulation rates may be attributed foremost to site-specific proximity to the river mouth (i.e., sediment source), variability in water depth, and enhanced sediment focusing at the Mississippi River canyon site. Trace element concentrations were first normalized to Al, and then Al-normalized enrichment factors (ANEF) were calculated based on preanthropogenic and crustal trace element abundances. These ANEFs were typically > 1 for V and Ba, while for most other elements studied, either no enrichment or depletion was observed. The enrichment of Ba may be related, in part, to the seasonal occurrence of oxygen-depleted subsurface waters off the Mississippi River delta, as well as being an ubiquitous by-product of the petroleum industry. ?? 2006 Estuarine Research Federation.

Light Stable Isotopic Compositions of Enriched Mantle Sources: Resolving the Dehydration Paradox

NASA Astrophysics Data System (ADS)

Dixon, J. E.; Bindeman, I. N.; Kingsley, R. H.

2017-12-01

An outstanding puzzle in mantle geochemistry has been the origin and evolution of Earth's volatile components. The "dehydration paradox" refers to the following conundrum. Mantle compositions for some enriched mid-ocean ridge (MORB) and ocean island (OIB) basalts basalts require involvement of a mostly dehydrated slab component to explain the trace element ratios and radiogenic isotopic compositions, but a fully hydrated slab component to explain the stable isotopic compositions. Volatile and stable isotopic data on enriched MORB show a diversity of enriched components. Pacific PREMA-type basalts (H2O/Ce = 215 ± 30, δDSMOW = -45 ± 5 ‰) are similar to those in the north Atlantic (H2O/Ce = 220 ± 30; δDSMOW = -30 to -40 ‰). Basalts with EM-type signatures have regionally variable volatile compositions. North Atlantic EM-type basalts are wetter (H2O/Ce = 330 ± 30) and have isotopically heavier hydrogen (δDSMOW = -57 ± 5 ‰) than north Atlantic MORB. South Atlantic EM-type basalts are damp (H2O/Ce = 120 ± 10) with intermediate δDSMOW (-68 ± 2 ‰), similar to dDSMOW for Pacific MORB. North EPR EM-type basalts are dry (H2O/Ce = 110 ± 20) and isotopically light (δDSMOW = -94 ± 3 ‰). Boron and lithium isotopic ratios parallel the trends observed for dDSMOW. A multi-stage metasomatic and melting model accounts for the origin of the enriched components by extending the subduction factory concept down through the mantle transition zone, with slab temperature a key variable. The dehydration paradox is resolved by decoupling of volatiles from lithophile elements, reflecting primary dehydration of the slab followed by secondary rehydration and re-equilibration by fluids derived from subcrustal hydrous phases (e.g., antigorite) in cooler, deeper parts of the slab. The "expanded subduction factory" model includes melting at several key depths, including 1) 180 to 280 km, where EM-type mantle compositions are generated above slabs with average to hot thermal profiles by addition of <1% carbonated sediment-derived supercritical fluids/melts to depleted asthenospheric or subcontinental lithospheric mantle, and 2) 410 to 660 km, where PREMA-type mantle sources are generated, above slabs with average to cool thermal profiles, by addition of <1% carbonated eclogite ± sediment-derived supercritical fluids to depleted mantle.

Metasomatic Control of Water in Garnet and Pyroxene from Kaapvaal Craton Mantle Xenoliths

NASA Technical Reports Server (NTRS)

Peslier, Anne H.; Woodland, Alan B.; Bell, David R.; Lazarov, Marina; Lapen, Thomas J.

2012-01-01

Fourier transform infrared spectrometry (FTIR) and laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) were used to determine water, rare earth (REE), lithophile (LILE), and high field strength (HFSE) element contents in garnet and pyroxene from mantle xenoliths, Kaapvaal craton, southern Africa. Water enters these nominally anhydrous minerals as protons bonded to structural oxygen in lattice defects. Pyroxene water contents (150-400 ppm in clinopyroxene; 40-250 ppm in orthopyroxene) correlate with their Al, Fe, Ca and Na and are homogeneous within a mineral grains and a xenolith. Garnets from Jagersfontein are chemically zoned for Cr, Ca, Ti and water contents. Garnets contain 0 to 20 ppm H2 Despite the fast diffusion rate of H in mantle m inerals, the observations above indicate that the water contents of mantle xenolith minerals were not disturbed during kimberlite entrainment and that the measured water data represent mantle values. Trace elements in all minerals show various degrees of light REE and LILE enrichments indicative of minimal to strong metasomatism. Water contents of peridotite minerals from the Kaapvaal lithosphere are not related to the degree of depletion of the peridotites. Instead, metasomatism exerts a clear control on the amount of water of mantle minerals. Xenoliths from each location record specific types of metasomatism with different outcomes for the water contents of mantle minerals. At pressures . 5.5 GPa, highly alkaline melts metasomatized Liqhobong and Kimberley peridotites, and increased the water contents of their olivine, pyroxenes and garnet. At higher pressures, the circulation of ultramafic melts reacting with peridotite resulted in co-variation of Ca, Ti and water at the edge of garnets at Jagersfontein, overall decreasing their water content, and lowered the water content of olivines at Finsch Mine. The calculated water content of these melts varies depending on whether the water content of the peridotite (2 wt% HO. 2O) or individual m inerals (<0.5-13 wt% H2O) are used, and also depend on the mineral-melt water partition coefficients. These metasomatic events are thought to have occurred during the Archean and Proterozoic, meaning that the water contents measured here have been preserved since that time and can be used to investigate viscocity and longevity of cratonic mantle roots.

Influence of Melting and Hydrothermal Alteration on Lead in Abyssal Peridotites

NASA Astrophysics Data System (ADS)

Warren, J. M.; D'Errico, M. E.; Godard, M.; Coble, M. A.; Horan, M.

2017-12-01

The lead isotopic system is a key tracer of mantle convection, yet the abundance and mineralogical hosts of Pb in the upper mantle are poorly constrained. To address this, we analyzed the concentration of Pb in minerals and bulk rock powders of abyssal peridotites. These samples represent the oceanic upper mantle following melt extraction. They can be used to explore the mantle Pb budget, assuming that the amount of Pb lost during mantle melting and gained during seafloor alteration can be determined. We performed in situ analysis of the three main silicate phases (olivine, orthopyroxene, and clinopyroxene), which yield Pb concentrations of 2-30 ppb. Olivine is the main mineralogical host of Pb, unlike other trace elements, which are predominantly hosted in clinopyroxene. Sulfide contains an average of 3 ppm Pb, but these high concentrations are offset by low modal abundances (<0.01%), making this mineral a minor source of peridotite Pb. Whole rock Pb concentrations of abyssal peridotites measured by thermal ionization mass spectrometry range from 3 to 38 ppb. These values are close to the reconstructed whole rock values of 2 to 14 ppb, calculated from the mineral concentrations of Pb multiplied by their modes. In contrast, the average value among literature data for whole rock abyssal peridotites is >100 ppb [1, 2], measured by inductively-coupled plasma mass spectrometry. The higher values among literature data may reflect a combination of lower analytical sensitivity and effects of alteration. Samples in this study include an unaltered peridotite from the Gakkel Ridge, which shows the closest agreement between reconstructed and measured whole rock values. We estimate that our peridotites have undergone 5 to 9% melting [3], based on non-modal fractional melt modeling of rare earth element abundances. Assuming 18 to 23 ppb Pb in the depleted source mantle [4, 5], expected concentrations in abyssal peridotites after melting are <1 ppb. However, as suggested by [5], mantle Pb abundance is poorly constrained by the Ce/Pb ratio of mid-ocean ridge basalt and the amount of Pb in the depleted mantle may be higher than current estimates. [1] Niu, 2004, J. Pet.; [2] Paulick et al., 2006, Chem. Geol.; [3] D'Errico et al., 2016, GCA; [4] Salters and Stracke, 2004, G-Cubed; [5] Workman and Hart, 2005 EPSL.

Lead Isotopes in Olivine-Phyric Shergottite Tissint: Implications for the Geochemical Evolution of the Shergottite Source Mantle

NASA Technical Reports Server (NTRS)

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

2015-01-01

Geochemically-depleted shergottites are basaltic rocks derived from a martian mantle source reservoir. Geochemical evolution of the martian mantle has been investigated mainly based on the Rb-Sr, Sm-Nd, and Lu-Hf isotope systematics of the shergottites [1]. Although potentially informative, U-Th- Pb isotope systematics have been limited because of difficulties in interpreting the analyses of depleted meteorite samples that are more susceptible to the effects of near-surface processes and terrestrial contamination. This study conducts a 5-step sequential acid leaching experiment of the first witnessed fall of the geochemically-depleted olivinephyric shergottite Tissint to minimize the effect of low temperature distrubence. Trace element analyses of the Tissint acid residue (mostly pyroxene) indicate that Pb isotope compositions of the residue do not contain either a martian surface or terrestrial component, but represent the Tissint magma source [2]. The residue has relatively unradiogenic initial Pb isotopic compositions (e.g., 206Pb/204Pb = 10.8136) that fall within the Pb isotope space of other geochemically-depleted shergottites. An initial µ-value (238U/204Pb = 1.5) of Tissint at the time of crystallization (472 Ma [3]) is similar to a time-integrated mu- value (1.72 at 472 Ma) of the Tissint source mantle calculated based on the two-stage mantle evolution model [1]. On the other hand, the other geochemically-depleted shergottites (e.g., QUE 94201 [4]) have initial µ-values of their parental magmas distinctly lower than those of their modeled source mantle. These results suggest that only Tissint potentially reflects the geochemical signature of the shergottite mantle source that originated from cumulates of the martian magma ocean

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.

Evaluating crustal contributions to enriched shergottites from the petrology, trace elements, and Rb-Sr and Sm-Nd isotope systematics of Northwest Africa 856

NASA Astrophysics Data System (ADS)

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

2017-08-01

The origin of the incompatible trace element (ITE) characteristics of enriched shergottites has been critical for examining two contradicting scenarios to explain how these Martian meteorites form. The first scenario is that it reflects ITE enrichment in an early-formed mantle reservoir whereas the second scenario attributes it to assimilation of ancient Martian crust (∼4-4.5 Ga) by ITE-depleted magmas. Strongly differentiated shergottite magmas may yield added constraints for determining which scenario can best explain this signature in enriched shergottites. The meteorite Northwest Africa (NWA) 856 is a basaltic shergottite that, unlike many enriched shergottites, lacks olivine and has undergone extensive differentiation from more primitive parent magma. In similarity to other basaltic shergottites, NWA 856 is comprised primarily of compositionally zoned clinopyroxenes (45% pigeonite and 23% augite), maskelynite (23%) and accessory minerals such as ulvöspinel, merrillite, Cl-apatite, ilmenite, pyrrhotite, baddeleyite and silica polymorph. The CI-chondrite normalized rare earth element (REE) abundance patterns for its maskelynite, phosphates, and its whole rock are flat with corresponding light-REE depletions in clinopyroxenes. The 87Rb-87Sr and 147Sm-143Nd internal isochron ages are 162 ± 14 (all errors are ±2σ) Ma and 162.7 ± 5.5 Ma, respectively, with an initial εNdI = -6.6 ± 0.2. The Rb-Sr isotope systematics are affected by terrestrial alteration resulting in larger scatter and a less precise internal isochron age. The whole rock composition is used in MELTS simulations to model equilibrium and fractional crystallization sequences to compare with the crystallization sequence from textural observations and to the mineral compositions. These models constrain the depth of initial crystallization to a pressure range of 0.4-0.5 GPa (equivalent to 34-42 km) in anhydrous conditions at the Fayalite-Magnetite-Quartz buffer, and consistently reproduce the observed mineralogy throughout the sequence with progressive crystallization. The Ti/Al ratios in the clinopyroxenes are consistent with initial crystallization occurring at these depths followed by polybaric crystallization as the parent magma ascended to the surface. The REE abundances in the clinopyroxenes and maskelynite are consistent with progressive crystallization in a closed system. The new results for NWA 856 are combined with other shergottite data and are compared to mixing and assimilation and fractional crystallization (AFC) models using depleted shergottite magmas and ancient Martian crust as end-members. The models indicate that the range of REE abundances and ratios, when taken in isolation, can be successfully explained for all shergottites by crustal contamination. However, no successful crustal contamination model can explain the restricted εNdI of -6.8 ± 0.2 over the wide range of Mg# (0.65-0.25), and corresponding trace element variations from enriched shergottites to depleted shergottites. The findings indicate that the origin of the long-term ITE-enriched signature in enriched shergottites and the geochemical variability seen in shergottites is not a result of crustal contamination but instead reflects ancient mantle heterogeneity.

Major and Trace Element Geochemistry and Os Isotopic Compositions of Komatiites From Dundonald Beach, Abitibi Greenstone Belt, Canada

NASA Astrophysics Data System (ADS)

Gangopadhyay, A.; Walker, R. J.; Sproule, R. A.; Lesher, C.

2003-12-01

We have examined the major and trace elements, and Os isotopic compositions of a suite of cumulate and spinifex textured komatiitic rocks from the Dundonald Beach area, part of the ˜2.7 Ga Abitibi greenstone Belt, Ontario, Canada. This suite of rocks forms a series from peridotitic komatiites (MgO ˜ 42 wt.% on a volatile-free basis) to komatiitic basalts (MgO ˜8 wt.%). Based on major element oxide ratios (e.g. Al2O3/TiO2 ˜21-26 and CaO/Al2O3 typically <= 1) and unfractionated HREE characteristics (e.g. (Gd/Yb)N ˜0.9-1.1), these rocks are similar to the spatially associated Al-undepleted komatiites from Alexo and Munro Townships. Also, these rocks are strongly LREE-depleted ((La/Sm)N = 0.41-0.67; (Ce/Yb)N = 0.41-0.70)) and have variable total REE (4-22 ppm). A strong negative correlation between Mg# and total REEs suggests that the REE patterns of these rocks are primary features of their mantle source. The Re-Os isotope results for whole-rock komatiites and chromite separates from a single flow yield a model 3 isochron age of 2606 +/- 55 Ma. This age is slightly younger ( ˜50 Ma) compared to the U-Pb zircon ages of the associated volcanics reported from the presumed extension of the same Kidd-Munro assemblage in Alexo and Munro Townships. The initial 187Os/188Os ratio (0.1090 +/- 0.0019) obtained from the regression is essentially chondritic (γ Os(T) = -0.2 +/- 1.7). The peridotitic komatiites have the highest Os concentrations and low 187Re/188Os ratios (up to ˜4.2 ppb and < 0.5, respectively) among the whole rocks, whereas the komatiitic basalts have relatively low Os concentrations ( ˜0.3 ppb) and high 187Re/188Os ratios ( ˜3.1-11.9). For these komatiites, Os was compatible with the mantle residue (DOsmantle-melt ˜7.6), whereas Re was moderately incompatible (DRe ˜0.6), typical of most komatiitic magmas. The absence of a strong correlation between Os and Ni concentrations in the whole-rocks suggests that the distribution of Os in these rocks is not primarily controlled by fractionation of olivine. The apparent DReol+chmt/liq. ( ˜0.7), on the other hand, suggests that Re was moderately incompatible in olivine and/or chromite during the differentiation of komatiitic magmas. A chondritic initial Os isotopic composition for the mantle source for these komatiites is consistent with that previously reported for the komatiites from Alexo and Munro Townships. Our Os isotopic results for Dundonald komatiites, combined with those reported for Alexo and Pyke Hill komatiites, therefore, suggest that a major portion of the ˜2.7 Ga mantle source for the komatiites in the Abitibi greenstone belt was dominated by Os with chondritic isotopic compositions. Also, the LREE-depleted, yet chondritic Os isotopic composition for the mantle source of these komatiites is indistinguishable from the projected chondritic composition of the contemporaneous depleted convective upper mantle.

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.

The influence of precipitation kinetics on trace element partitioning between solid and liquid solutions: A coupled fluid dynamics/thermodynamics framework to predict distribution coefficients

NASA Astrophysics Data System (ADS)

Kavner, A.

2017-12-01

In a multicomponent multiphase geochemical system undergoing a chemical reaction such as precipitation and/or dissolution, the partitioning of species between phases is determined by a combination of thermodynamic properties and transport processes. The interpretation of the observed distribution of trace elements requires models integrating coupled chemistry and mechanical transport. Here, a framework is presented that predicts the kinetic effects on the distribution of species between two reacting phases. Based on a perturbation theory combining Navier-Stokes fluid flow and chemical reactivity, the framework predicts rate-dependent partition coefficients in a variety of different systems. We present the theoretical framework, with applications to two systems: 1. species- and isotope-dependent Soret diffusion of species in a multicomponent silicate melt subjected to a temperature gradient, and 2. Elemental partitioning and isotope fractionation during precipitation of a multicomponent solid from a multicomponent liquid phase. Predictions will be compared with results from experimental studies. The approach has applications for understanding chemical exchange in at boundary layers such as the Earth's surface magmatic systems and at the core/mantle boundary.

Galapagos hotspot-spreading center system: 1. Spatial petrological and geochemical variations (83/sup 0/W-101/sup 0/W)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Schilling, J.; Kingsley, R.H.; Devine, J.D.

We report on the petrology and geochemistry of basalts dredged at 40--50 km intervals along the Galapagos Spreading Center, between 83/sup 0/W and 101/sup 0/W (40 stations). Emphasis is on spatial variations of 'whole rock' major elements, rare earths, trace metals of the first transition series, and the nature of phenocryst assemblages and their abundances. These results provide new constraints on the nature and scale of mantle source heterogeneities, melting conditions, thermal field, and dynamics of crustal formation of the region. We suggest that ridge segments outside the high magnetic amplitude zone are at a steady state as a resultmore » of passive seafloor spreading. Basalts from these segments are apparently derived from an asthenosphere relatively uniformally depleted in incompatible elements, which appears of worldwide extent. We reject Vogt and DeBoer's (1976) model invoking damming at fracture zones of subaxial asthenosphere flow of crystal slushes and increasing fractional crystallization down the flow line, because this model would not explain the gradients in REE observed about the Galapagos Platform. Our preferred model combines the mantle-plume binary mixing model of Schilling (1973) with the concept of recurring rift propagation proposed by Hey (1977a). We further propose that pulsating mantle plume flux, perhaps in the form of a chain of blobs, may initiate the development of new rifts and their propagation. The present position of the tips of such new propagating rifts locate the wave fronts of such pulsating mantle plume flow. A two million year period is suggested for the last 4 m.y. from Wilson and Hey's (1979) information Rigorous testing of our preferred model is possible.« less