Chondrule heritage and thermal histories from trace element and oxygen isotope analyses of chondrules and amoeboid olivine aggregates

NASA Astrophysics Data System (ADS)

Jacquet, Emmanuel; Marrocchi, Yves

2017-12-01

We report combined oxygen isotope and mineral-scale trace element analyses of amoeboid olivine aggregates (AOA) and chondrules in ungrouped carbonaceous chondrite, Northwest Africa 5958. The trace element geochemistry of olivine in AOA, for the first time measured by LA-ICP-MS, is consistent with a condensation origin, although the shallow slope of its rare earth element (REE) pattern is yet to be physically explained. Ferromagnesian silicates in type I chondrules resemble those in other carbonaceous chondrites both geochemically and isotopically, and we find a correlation between 16O enrichment and many incompatible elements in olivine. The variation in incompatible element concentrations may relate to varying amounts of olivine crystallization during a subisothermal stage of chondrule-forming events, the duration of which may be anticorrelated with the local solid/gas ratio if this was the determinant of oxygen isotopic ratios as proposed recently. While aqueous alteration has depleted many chondrule mesostases in REE, some chondrules show recognizable subdued group II-like patterns supporting the idea that the immediate precursors of chondrules were nebular condensates.

Magma Differentiation Processes That Develop an "Enriched" Signature in the Izu Bonin Rear Arc: Evidence from Drilling at IODP Site U1437

NASA Astrophysics Data System (ADS)

Heywood, L. J.; DeBari, S. M.; Schindlbeck, J. C.; Escobar-Burciaga, R. D.

2015-12-01

The Izu Bonin rear arc represents a unique laboratory to study the development of continental crust precursors at an intraoceanic subduction zone., Volcanic output in the Izu Bonin rear arc is compositionally distinct from the Izu Bonin main volcanic front, with med- to high-K and LREE-enrichment similar to the average composition of the continental crust. Drilling at IODP Expedition 350 Site U1437 in the Izu Bonin rear arc obtained volcaniclastic material that was deposited from at least 13.5 Ma to present. IODP Expedition 350 represents the first drilling mission in the Izu Bonin rear arc region. This study presents fresh glass and mineral compositions (obtained via EMP and LA-ICP-MS) from unaltered tephra layers in mud/mudstone (Lithostratigraphic Unit I) and lapillistone (Lithostratigraphic Unit II) <4.5 Ma to examine the geochemical signature of Izu Bonin rear arc magmas. Unit II samples are coarse-grained tephras that are mainly rhyolitic in composition (72.1-77.5 wt. % SiO2, 3.2-3.9 wt. % K2O and average Mg# 24) and LREE-enriched. These rear-arc rhyolites have an average La/Sm of 2.6 with flat HREEs, average Th/La of 0.15, and Zr/Y of 4.86. Rear-arc rhyolite trace element signature is distinct from felsic eruptive products from the Izu Bonin main volcanic front, which have lower La/Sm and Th/La as well as significantly lower incompatible element concentrations. Rear arc rhyolites have similar trace element ratios to rhyolites from the adjacent but younger backarc knolls and actively-extending rift regions, but the latter is typified by lower K2O, as well as a smaller degree of enrichment in incompatible elements. Given these unique characteristics, we explore models for felsic magma formation and intracrustal differentiation in the Izu Bonin rear arc.

Post-collisional subvolcanic rhyolites associated with the Neoproterozoic Pelotas Batholith, southern Brazil

NASA Astrophysics Data System (ADS)

Oliveira, Diego Skieresz de; Sommer, Carlos Augusto; Philipp, Ruy Paulo; Lima, Evandro Fernandes de; Basei, Miguel Ângelo Stipp

2015-11-01

Neoproterozoic volcanic and subvolcanic rhyolitic systems in southernmost Brazil are correlated with acid magmatism linked to different petrotectonic associations of the Sul-Rio-Grandense Shield. A portion of this volcanism in the Dom Feliciano Belt is associated with the Pelotas Batholith, which resulted from magmatic episodes associated with the Ediacaran post-collisional evolution of southern Brazil. Ana Dias Rhyolite is the main subvolcanic occurrence of this volcanism that took place in the Quitéria region, in the central part of Rio Grande do Sul State. The acid magmatism has been commonly associated with the most differentiated granite suite phases during the final stages of emplacement of the Pelotas Batholith. The Ana Dias Rhyolite is characterized as an intrusive body with rocks that present a porphyritic to seriated texture and a gradational variation to fine-grained equigranular rocks. New zircon U-Pb dating indicates crystallization age of 581.9 ± 1.9 Ma for the Ana Dias Rhyolite. Geochemistry data characterize the rhyolites as belonging to the alkaline series; they present a metaluminous to peraluminous character; elevated SiO2 and alkali concentrations, high FeOt/FeOt + MgO ratios and agpaitic index; and low Al2O3, CaO, and MgO contents. The Zr, Rb, Y, Nb, and Ga concentrations are moderate when compared with the relatively low Ba and Sr contents. These geochemistry characteristics are common in acid magmas with alkaline affinity. The behavior of certain trace elements and REE demonstrate enrichment in more incompatible elements, in addition to the negative anomaly of Ba, the slight enrichment in Ce relative to adjacent elements, as well as the enrichment in K2O and Rb relative to Nb, suggesting magmas derived from mantle sources enriched in incompatible elements with some crustal contamination. The chemical characteristics are similar to those of A-type granites associated with Neoproterozoic post-collision magmatism in the Sul-Rio-Grandense Shield.

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.

Geochemistry of zircons from basic rocks of the Korosten anorthosite-mangerite-charnockite-granite complex, north-western region of the Ukrainian Shield

NASA Astrophysics Data System (ADS)

Shumlyanskyy, Leonid; Belousova, Elena; Petrenko, Oksana

2017-09-01

The concentrations of 26 trace elements have been determined by laser ablation ICP-MS in zircons from four samples of basic rocks of the Korosten anorthosite-mangerite-charnockite-granite plutonic complex, the Ukrainian Shield. Zircons from the Fedorivka and Torchyn gabbroic intrusions and Volynsky anorthosite massif have distinctive abundances of many trace elements (REE, Sr, Y, Mn, Th). Zircons from the gabbroic massifs are unusually enriched in trace elements, while zircons from pegmatites in anorthosite are relatively depleted in trace elements. High concentrations of trace elements in zircons from gabbroic intrusions can be explained by their crystallization from residual interstitial melts enriched in incompatible elements. The zircons studied demonstrate a wide range of Ti concentrations, which reflects their temperature of crystallization: the zircons most enriched in Ti, from mafic pegmatites of the Horbuliv quarry (20-40 ppm), have the highest temperature of crystallization (845 ± 40 °C). Lower (720-770 °C) temperatures of zircon crystallization in gabbroic rocks are explained by its crystallization from the latest portions of the interstitial melt or by simultaneous crystallization of ilmenite. The Ce anomaly in zircons correlates with the degree of oxidation of the coexisting ilmenite.

The behavior and concentration of CO2 in the suboceanic mantle: Inferences from undegassed ocean ridge and ocean island basalts

NASA Astrophysics Data System (ADS)

Michael, Peter J.; Graham, David W.

2015-11-01

In order to better determine the behavior of CO2 relative to incompatible elements, and improve the accuracy of mantle CO2 concentration and flux estimates, we determined CO2 glass and vesicle concentrations, plus trace element contents for fifty-one ultradepleted mid-ocean ridge basalt (MORB) glasses from the global mid-ocean ridge system. Fifteen contained no vesicles and were volatile undersaturated for their depth of eruption. Thirty-six contained vesicles and/or were slightly oversaturated, and so may not have retained all of their CO2. If this latter group lost some bubbles during emplacement, then CO2/Ba calculated for the undersaturated group alone is the most reliable and uniform ratio at 98 ± 10, and CO2/Nb is 283 ± 32. If the oversaturated MORBs did not lose bubbles, then CO2/Nb is the most uniform ratio within the entire suite of ultradepleted MORBs at 291 ± 132, while CO2/Ba decreases with increasing incompatible element enrichment. Additional constraints on CO2/Ba and CO2/Nb ratios are provided by published estimates of CO2 contents in highly vesicular enriched basalts that may have retained their vesicles e.g., the Mid-Atlantic Ridge "popping rocks", and from olivine-hosted melt inclusions in normal MORBs. As incompatible element enrichment increases, CO2/Nb increases progressively from 283 ± 32 in ultradepleted MORBs to 603 ± 69 in depleted melt inclusions to 936 ± 132 in enriched, vesicular basalts. In contrast, CO2/Ba is nearly uniform in these sample suites at 98 ± 10, 106 ± 24 and 111 ± 11 respectively. This suggests that Ba is the best proxy for estimating CO2 contents of MORBs, with an overall average CO2/Ba = 105 ± 9. Atlantic, Pacific and Indian basalts have similar values. Gakkel Ridge has lower CO2/Ba because of anomalously high Ba, and is not included in our global averages. Using the CO2/Ba ratio and published compilations of trace elements in average MORBs, the CO2 concentration of a primary, average MORB is 2085+ 473/- 427 ppm, while primary NMORB magmas (> 500 km from ocean island hotspots) have 1840 ppm CO2. The annual flux of CO2 from mid-ocean ridges is 1.25 ± 0.16 × 1014 g/yr, with possible values as low as 0.93 and as high as 1.61 × 1014 g/yr. This amount is equivalent to approximately 0.3% of the anthropogenic addition of CO2 to Earth's atmosphere. NMORB mantle has 183 ppm CO2 (50 ppm C) based on simple melting models and 13% melting. More realistic estimates of incompatible element concentrations in the depleted mantle that are consistent with complex melting models yield much lower estimates for CO2 in the depleted mantle: around 60-130 ppm CO2, with large uncertainties that are more related to melting models than to CO2/Ba. CO2/Ba is not correlated with isotopic or trace element ratios, but there may be systematic regional mantle variations. Iceland melt inclusions and Gakkel Ridge MORBs have lower CO2/Ba ratios, showing that these regional high Ba anomalies are not accompanied by correspondingly high CO2 concentrations.

Geochemistry 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.

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).

Chlorine in Lunar Basalts

NASA Technical Reports Server (NTRS)

Barnes, J. J.; Anand, M.; Franchi, I. A.

2017-01-01

In the context of the lunar magma ocean (LMO) model, it is anticipated that chlorine (and other volatiles) should have been concentrated in the late-stage LMO residual melts (i.e., the dregs enriched in incompatible elements such as K, REEs, and P, collectively called KREEP, and in its primitive form - urKREEP, [1]), given its incompatibility in mafic minerals like olivine and pyroxene, which were the dominant phases that crystallized early in the cumulate pile of the LMO (e.g., [2]). When compared to chondritic meteorites and terrestrial rocks (e.g., [3-4]), lunar samples often display heavy chlorine isotope compositions [5-9]. Boyce et al. [8] found a correlation between delta Cl-37 (sub Ap) and bulk-rock incompatible trace elements (ITEs) in lunar basalts, and used this to propose that early degassing of Cl (likely as metal chlorides) from the LMO led to progressive enrichment in remaining LMO melt in Cl-37over Cl-35- the early degassing model. Barnes et al. [9] suggested that relatively late degassing of chlorine from urKREEP (to yield delta Cl-37 (sub urKREEP greater than +25 per mille) followed by variable mixing between KREEPy melts and mantle cumulates (characterized by delta Cl-370 per mille) could explain the majority of Cl isotope data from igneous lunar samples. In order to better understand the processes involved in giving rise to the heavy chlorine isotope compositions of lunar samples, we have performed an in situ study of chlorine isotopes and abundances of volatiles in lunar apatite from a diverse suite of lunar basalts spanning a range of geochemical types.

Trace and rare-earth element characteristics of acidic tuffs from southern Peru and northern Bolivia and a fission-track age for the sillar of Arequipa

NASA Astrophysics Data System (ADS)

Vatin-Perignon, N.; Poupeau, G.; Oliver, R. A.; La Venu, A.; Labrin, F.; Keller, F.; Bellot-Gurlet, L.

1996-03-01

Trace-element and REE data of glass and pumices of acidic tuffs and related fall deposits erupted in southern Peru and northern Bolivia between 20 and 0.36 Ma display typical characteristics of subduction related continental arc magmatism of the CVZ with strong LILE/HFSE enrichment and non enrichment of HREE and Y. Geochemical variations of these tuffs are linked to subduction processes and controlled by changes in tectonic regimes which occured with each Quechua tectonic pulse and affected the astenospheric wedge and both the dowgoing and the overriding lithospheres. During Neogene — Pleistocene times, tuffs erupted in northern Bolivia are typically enriched in Zr, Hf, Th, Ba, LREEs and other incompatible elements and incompatible /Yb ratios are much higher relative to those erupted from southern Peru, at a given SiO 2 content (65-67 wt. for dacites, 72-73 wt.% for rhyolites). {Zr}/{Hf} ratios increase eastward from 27 to 30 and {Ce}/{Yb N} ratios from 11 to 19 reflecting the variation of degree of wedge contribution. Fractionation of the LREE over the HREE and fractionation of incompatible elements may be due to their heterogeneous distribution in the magma source. More highly fractionated REE patterns of Bolivian tuffs than Peruvian tuffs are attributed to variable amounts of contamination of magmas by lower crust. After the Quechua compressional event at 7 Ma, {Sr}/{Y} ratios of tuffs of the same age, erupted at 150-250 km or 250-400 km from the Peru-Chile trench, increase from southern Peru to northern Bolivia. These differences may be attributed to the subduction of a swarm oceanic lithosphere under the Bolivian Alti-plano, leading to partial melting of the sudbucted lithosphere. New FT dating of obsidian fragments of the sillar of Arequipa at 2.42 ± 0.11 Ma. This tuff dates the last Quechua compressional upper Pliocene phase ( 2.5 Ma) and confirms that the sillar is not contemporaneous with the Toba 76 tuff or the Perez ignimbrite of northern Bolivia. Geochemical characteristics of tuffs erupted before and after this last compressional phase remained the same and provide evidence that the upper Miocene ( 7 Ma) compressional deformations played the most important role on the variability of the geochemical characteristics of the southern Peruvian and northern Bolivian tuffs.

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.

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.

Dynamical Geochemistry

NASA Astrophysics Data System (ADS)

Davies, G. F.

2009-12-01

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

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.

Concentration, behavior and storage of H/sub 2/O in the suboceanic upper mantle: implications for mantle metasomatism

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

Michael, P.J.

1988-02-01

Mid-ocean ridge basalt glasses from the Pacific-Nazca Ridge and the northern Juan de Fuca Ridge were analyzed for H/sub 2/O by gas chromatography. Incompatible element enriched (IEE) glasses have higher H/sub 2/O contents than depleted (IED) glasses. H/sub 2/O increases systematically with decreasing Mg/Mg + Fe/sup 2 +/ within each group. Near-primary IED MORBs have an average of about 800 ppm H/sub 2/O, while near-primary IEE MORBs (with chondrite normalized Nb/Zr or La/Sm approx. 2) have about 2100 ppm H/sub 2/O. If these basalts formed by 10-20% partial melting then the IED mantle source had 100-180 ppm H/sub 2/O, whilemore » the IEE source had 250-450 ppm H/sub 2/O. The ratio H/sub 2/O/(Ce + Nd) is fairly constant at 95 +/- 30 for all oceanic basalts from the Pacific. During trace element fractionation in the suboceanic upper mantle, H/sub 2/O behaves more compatibly than K, Rb, Nb, and Cl, but less compatibly than Sm, Zr and Ti. H/sub 2/O is contained mostly in amphibole in the shallow upper mantle. At pressures greater than the amphibole stability limit, it is likely that a significant proportion of H/sub 2/O is contained in a mantle phase which is more refractory than phlogopite at these pressures. The role of H/sub 2/O in mantle enrichment processes is examined by assuming that an enriched component was added. The modeled concentrations of K, Na, Ti and incompatible trace elements in this component are high relative to H/sub 2/O, indicating that suboceanic mantle enrichment is caused by silicate melts such as basanites and not by aqueous fluids.« less

Fractionation of palladium and platinum in a Mesozoic diabase sheet, Gettysburg basin, Pennsyvania: implications for mineral exploration

USGS Publications Warehouse

Gottfried, D.; Froelich, A.J.; Rait, N.; Aruscavage, P. J.

1990-01-01

The York Haven diabase sheet displays clear-cut evidence of fractionation of Pd and Pt during differentiation of a high-Ti (about 1.1%) quartz-normative tholeiitic magma (York Haven type). At York Haven the sheet is about 750 m thick. It is characterized by abundant cumulus MgO-rich orthopyroxene (bronzite), and is markedly depleted in incompatible elements relative to the chilled margins. In contrast, at Reesers Summit, 16 km to the northwest, the sheet is about 500 m thick and consists of evolved rocks that have contents of incompatible elements two to three times greater than in the enclosing chilled margins. These evolved rocks represent complementary fractions to the cumulate rocks at York Haven. Mineralogic, petrologic and geochemical variations suggest considerable lateral migration and fractionation of the initial magma. Chilled margins of both sections have essentially the same Pd and Pt contents (10 ppb each) and similar Pd to Pt ratios (1.2). During differentiation, the cumulate rocks at York Haven were enriched in Pt and depleted in Pd, whereas at Reesers Summit, the low-MgO diabase and ferrogabbro zone were enriched in Pd relative to Pt. Anomalously high contents of Pd (to 165 ppb), Au (to 54 ppb), and Te (to 26 ppb) were found in an iron- (to 18%) and chlorine- (to 0.44%) rich ferrogabbro at Reesers Summit, suggesting possible late or post-magmatic enrichment of precious metals. Field relations, geochemical and petrographic data provide guides for further exploration for Pd and Pt in differentiated high-Ti quartz-normative diabase sheets. Based on present information, the most favorable sites for economic deposits are late-stage differentiates enriched in Fe and Cl. ?? 1990.

Carbonatite magmatism in northeast India

NASA Astrophysics Data System (ADS)

Kumar, D.; Mamallan, R.; Dwivedy, K. K.

The Shillong Plateau of northeast India is identified as an alkaline province in view of the development of several carbonatite complexes e.g. the Sung Valley (Jaintia Hills), Jasra (Karbi-Anglong), Samchampi and Barpung (Mikir Hills) and lamprophyre dyke swarms (Swangkre, Garo-Khasi Hills). On the basis of limited KAr data, magmatic activity appears to have taken place over a protracted period, ranging from the Late Jurassic to the Early Cretaceous. The carbonatite complexes of the Shillong Plateau share several common traits: they are emplaced along rift zones, either within Archaean gneisses or Proterozoic metasediments and granites, and exhibit enrichment in the light rare-earth elements, U, Th, Nb, Zr, Ti, K and Na. The enrichment in incompatible trace elements can best be accounted for if the parental magmas were of alkali basaltic type (e.g. mela-nephelinite or carbonate-rich alkali picrite).

The Finero phlogopite-peridotite massif: an example of subduction-related metasomatism

NASA Astrophysics Data System (ADS)

Zanetti, Alberto; Mazzucchelli, Maurizio; Rivalenti, Giorgio; Vannucci, Riccardo

The Finero peridotite massif is a harzburgite that suffered a dramatic metasomatic enrichment resulting in the pervasive presence of amphibole and phlogopite and in the sporadic occurrence of apatite and carbonate (dolomite)-bearing domains. Pyroxenite (websterite) dykes also contain phlogopite and amphibole, but are rare. Peridotite bulk-rock composition retained highly depleted major element characteristics, but was enriched in K, Rb, Ba, Sr, LREE (light rare earth elements) (LaN/YbN=8-17) and depleted in Nb. It has high radiogenic Sr (87Sr/86Sr(270)=0.7055-0.7093), low radiogenic Nd (ɛNd(270)=-1 to -3) and EMII-like Pb isotopes. Two pyroxenite - peridotite sections examined in detail show the virtual absence of major and trace element gradients in the mineral phases. In both rock types, pyroxenes and olivines have the most unfertile major element composition observed in Ivrea peridotites, spinels are the richest in Cr, and amphibole is pargasite. Clinopyroxenes exhibit LREE-enriched patterns (LaN/YbN 16), negative Ti and Zr and generally positive Sr anomaly. Amphibole has similar characteristics, except a weak negative Sr anomaly, but incompatible element concentration 1.9 (Sr) to 7.9 (Ti) times higher than that of coexisting clinopyroxene. Marked geochemical gradients occur toward apatite and carbonate-bearing domains which are randomly distributed in both the sections examined. In these regions, pyroxenes and amphibole (edenite) arelower in mg## and higher in Na2O, and spinels and phlogopite are richer in Cr2O3. Both the mineral assemblage and the incompatible trace element characteristics of the mineral phases recall the typical signatures of ``carbonatite'' metasomatism (HFSE depletion, Sr, LILE and LREE enrichment). Clinopyroxene has higher REE and Sr concentrations than amphibole (amph/cpxDREE,Sr=0.7-0.9) and lower Ti and Zr concentrations. It is proposed that the petrographic and geochemical features observed at Finero are consistent with a subduction environment. The lack of chemical gradients between pyroxenite and peridotite is explained by a model where melts derived from an eclogite-facies slab infiltrate the overhanging harzburgitic mantle wedge and, because of the special thermal structure of subduction zones, become heated to the temperature of the peridotite. If the resulting temperature is above that of the incipient melting of the hydrous peridotite system, the slab-derived melt equilibrates with the harzburgite and a crystal mush consisting of harzburgite and a silica saturated, hydrous melt is formed. During cooling, the crystal mush crystallizes producing the observed sequence of mineral phases and their observed chemical characteristics. In this context pyroxenites are regions of higher concentration of the melt in equilibrium with the harzburgite and not passage-ways through which exotic melts percolated. Only negligible chemical gradients can appear as an effect of the crystallization process, which also accounts for the high amphibole/clinopyroxene incompatible trace element ratios. The major element refractory composition is explained by an initially high peridotite/melt ratio. The apatite, carbonate-bearing domains are the result of the presence of some CO2 in the slab-derived melt. The CO2/H2O ratio in the peridotite mush increased by crystallization of hydrous phases (amphibole and phlogopite) locally resulting in the unmixing of a late carbonate fluid. The proposed scenario is consistent with subduction of probably Variscan age and with the occurrence of modal metasomatism before peridotite incorporation in the crust.

Geochemistry and petrogenesis of lamproites, late cretaceous age, Woodson County, Kansas, U.S.A.

USGS Publications Warehouse

Cullers, R.L.; Ramakrishnan, S.; Berendsen, P.; Griffin, T.

1985-01-01

Lamproite sills and their associated sedimentary and contact metamorphic rocks from Woodson County, Kansas have been analyzed for major elements, selected trace elements, and strontium isotopic composition. These lamproites, like lamproites elsewhere, are alkalic (molecular K2O + Na2O Al2O3 = 1.6-2.6), are ultrapotassic ( K2O Na2O = 9.6-150), are enriched in incompatible elements (LREE or light rare-earth elements, Ba, Th, Hf, Ta, Sr, Rb), and have moderate to high initial strontium isotopic compositions (0.7042 and 0.7102). The silica-saturated magma (olivine-hypersthene normative) of the Silver City lamproite could have formed by about 2 percent melting of a phlogopite-garnet lherzolite under high H2O CO2 ratios in which the Iherzolite was enriched before melting in the incompatible elements by metasomatism. The Rose Dome lamproite probably formed in a similar fashion although the extreme alteration due to addition of carbonate presumably from the underlying limestone makes its origin less certain. Significant fractional crystallization of phases that occur as phenocrysts (diopside, olivine, K-richterite, and phlogopite) in the Silver City magma and that concentrate Co, Cr, and Sc are precluded as the magma moved from the source toward the surface due to the high abundances of Co, Cr, and Sc in the magma similar to that predicted by direct melting of the metasomatized Iherzolite. Ba and, to a lesser extent, K and Rb and have been transported from the intrusions at shallow depth into the surrounding contact metamorphic zone. The Silver City lamproite has vertical fractionation of some elements due either to volatile transport or to variations in the abundance of phenocrysts relative to groundmass most probably due to flow differentiation although multiple injection or fractional crystallization cannot be conclusively rejected. ?? 1985.

Evidence against a chondritic Earth.

PubMed

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

2012-03-28

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

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.

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

NASA Astrophysics Data System (ADS)

Valer, Marina; Schiano, Pierre; Bachèlery, Patrick

2017-09-01

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

Turbidite geochemistry and evolution of the Izu-Bonin arc and continents

NASA Astrophysics Data System (ADS)

Gill, J. B.; Hiscott, R. N.; Vidal, Ph.

1994-10-01

The major and trace element and NdPb isotopic composition of Oligocene to Pleistocene volcaniclastic sands and sandstones derived from the Izu Bonin island arc has been determined. Many characteristics of the igneous sources are preserved and record the geochemical evolution of juvenile proto-continental crust in an island arc. After an initial boninitic phase, arc geochemistry has varied primarily as the result of backarc basin formation. The Izu arc source became depleted in incompatible trace elements during backarc basin formation, and re-enriched after spreading stopped in the basin. Renewed rifting during the Pliocene to Recent caused felsic magmatism as a result of easier eruption of differentiates rather than as a result of crustal melting. Four isotopically-distinct source components are recognized. Their combination in the sources of the Izu-Bonin and Mariana arcs initially was similar but diverged after backarc basin formation. The Izu arc turbidites are more similar to Archean than post-Archean sedimentary rocks, indicating that the production of new upper crust at subduction zones has changed little over time. The turbidites are similar in major element composition to average continental crust but are depleted in incompatible trace elements, especially Th and Nb. Consequently, the net effect of adding juvenile arc crust to continents is to reverse the trend of planetary trace element differentiation instead of continuing the process.

The Transcriptional Response to Nonself in the Fungus Podospora anserina

PubMed Central

Bidard, Frédérique; Clavé, Corinne; Saupe, Sven J.

2013-01-01

In fungi, heterokaryon incompatibility is a nonself recognition process occurring when filaments of different isolates of the same species fuse. Compatibility is controlled by so-called het loci and fusion of strains of unlike het genotype triggers a complex incompatibility reaction that leads to the death of the fusion cell. Herein, we analyze the transcriptional changes during the incompatibility reaction in Podospora anserina. The incompatibility response was found to be associated with a massive transcriptional reprogramming: 2231 genes were up-regulated by a factor 2 or more during incompatibility. In turn, 2441 genes were down-regulated. HET, NACHT, and HeLo domains previously found to be involved in the control of heterokaryon incompatibility were enriched in the up-regulated gene set. In addition, incompatibility was characterized by an up-regulation of proteolytic and other hydrolytic activities, of secondary metabolism clusters and toxins and effector-like proteins. The up-regulated set was found to be enriched for proteins lacking orthologs in other species and chromosomal distribution of the up-regulated genes was uneven with up-regulated genes residing preferentially in genomic islands and on chromosomes IV and V. There was a significant overlap between regulated genes during incompatibility in P. anserina and Neurospora crassa, indicating similarities in the incompatibility responses in these two species. Globally, this study illustrates that the expression changes occurring during cell fusion incompatibility in P. anserina are in several aspects reminiscent of those described in host-pathogen or symbiotic interactions in other fungal species. PMID:23589521

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.

Orthopyroxene oikocrysts in the MG1 chromitite layer of the Bushveld Complex: implications for cumulate formation and recrystallisation

NASA Astrophysics Data System (ADS)

Kaufmann, Felix E. D.; Vukmanovic, Zoja; Holness, Marian B.; Hecht, Lutz

2018-02-01

Two typical mineral textures of the MG 1 chromitite of the Bushveld Complex, South Africa, were observed; one characterised by abundant orthopyroxene oikocrysts, and the other by coarse-grained granular chromitite with only minor amounts of interstitial material. Oikocrysts form elongate clusters of several crystals aligned parallel to the layering, and typically have subhedral, almost chromite-free, core zones containing remnants of olivine. The core zones are surrounded by poikilitic aureoles overgrowing euhedral to subhedral chromite chadacrysts. Chromite grains show no preferred crystal orientation, whereas orthopyroxene grains forming clusters commonly share the same crystallographic orientation. Oikocryst core zones have lower Mg# and higher concentrations of incompatible trace elements compared to their poikilitic aureoles. Core zones are relatively enriched in REE compared to a postulated parental magma (B1) and did not crystallise in equilibrium with the surrounding minerals, whereas the composition of the poikilitic orthopyroxene is consistent with growth from the B1 magma. These observations cannot be explained by the classic cumulus and post-cumulus models of oikocryst formation. Instead, we suggest that the oikocryst core zones in the MG1 chromitite layer formed by peritectic replacement of olivine primocrysts by reaction with an upwards-percolating melt enriched in incompatible trace elements. Poikilitic overgrowth on oikocryst core zones occurred in equilibrium with a basaltic melt of B1 composition near the magma-crystal mush interface. Finally, adcumulus crystallisation followed by grain growth resulted in the surrounding granular chromitite.

Geochemistry of Archean shales from the Pilbara Supergroup, Western Australia

NASA Astrophysics Data System (ADS)

McLennan, Scott M.; Taylor, S. R.; Eriksson, K. A.

1983-07-01

Archean clastic sedimentary rocks are well exposed in the Pilbara Block of Western Australia. Shales from turbidites in the Gorge Creek Group ( ca. 3.4 Ae) and shales from the Whim Creek Group ( ca. 2.7 Ae) have been examined. The Gorge Creek Group samples, characterized by muscovite-quartzchlorite mineralogy, are enriched in incompatible elements (K, Th, U, LREE) by factors of about two, when compared to younger Archean shales from the Yilgarn Block. Alkali and alkaline earth elements are depleted in a systematic fashion, according to size, when compared with an estimate of Archean upper crust abundances. This depletion is less notable in the Whim Creek Group. Such a pattern indicates the source of these rocks underwent a rather severe episode of weathering. The Gorge Creek Group also has fairly high B content (85 ± 29 ppm) which may indicate normal marine conditions during deposition. Rare earth element (REE) patterns for the Pilbara samples are characterized by light REE enrichment ( La N/Yb N ≥ 7.5 ) and no or very slight Eu depletion ( Eu/Eu ∗ = 0.82 - 0.99 ). A source comprised of about 80% felsic igneous rocks without large negative Eu-anomalies (felsic volcanics, tonalites, trondhjemites) and 20% mafic-ultramafic volcanics is indicated by the trace element data. Very high abundances of Cr and Ni cannot be explained by any reasonable provenance model and a secondary enrichment process is called for.

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

NASA Astrophysics Data System (ADS)

Sun, C.; Dasgupta, R.

2017-12-01

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

Transformation of juvenile Izu-Bonin-Mariana oceanic arc into mature continental crust: An example from the Neogene Izu collision zone granitoid plutons, Central Japan

NASA Astrophysics Data System (ADS)

Saito, Satoshi; Tani, Kenichiro

2017-04-01

Granitic rocks (sensulato) are major constituents of upper continental crust. Recent reviews reveal that the average composition of Phanerozoic upper continental crust is granodioritic. Although oceanic arcs are regarded as a site producing continental crust material in an oceanic setting, intermediate to felsic igneous rocks occurring in modern oceanic arcs are dominantly tonalitic to trondhjemitic in composition and have lower incompatible element contents than the average upper continental crust. Therefore, juvenile oceanic arcs require additional processes in order to get transformed into mature continental crust enriched in incompatible elements. Neogene granitoid plutons are widely exposed in the Izu Collision Zone in central Japan, where the northern end of the Izu-Bonin-Mariana (IBM) arc (juvenile oceanic arc) has been colliding with the Honshu arc (mature island arc) since Middle Miocene. The plutons in this area are composed of various types of granitoids ranging from tonalite to trondhjemite, granodiorite, monzogranite and granite. Three main granitoid plutons are distributed in this area: Tanzawa plutonic complex, Kofu granitic complex, and Kaikomagatake granitoid pluton. Tanzawa plutonic complex is dominantly composed of tonalite and trondhjemite and characterized by low concentration of incompatible elements and shows geochemical similarity with modern juvenile oceanic arcs. In contrast, Kofu granitic complex and Kaikomagatake granitoid pluton consists mainly of granodiorite, monzogranite and granite and their incompatible element abundances are comparable to the average upper continental crust. Previous petrogenetic studies on these plutons suggested that (1) the Tanzawa plutonic complex formed by lower crustal anatexis of juvenile basaltic rocks occurring in the IBM arc, (2) the Kofu granitic complex formed by anatexis of 'hybrid lower crust' comprising of both basaltic rocks of the IBM arc and metasedimentary rocks of the Honshu arc, and (3) the Kaikomagatake granitoid pluton formed by anatexis of 'hybrid lower crust' consisting of K-rich rear-arc crust of the IBM arc and metasedimentary rocks of the Honshu arc. These studies collectively suggest that the chemical diversity within the Izu Collision Zone granitoid plutons reflects the chemical variation of basaltic sources (i.e., across-arc chemical variation in the IBM arc) as well as variable contribution of the metasedimentary component in the source region. The petrogenetic models of the Izu Collision Zone granitoid plutons suggest that collision with another mature arc/continent, hybrid lower crust formation and subsequent hybrid source anatexis are required for juvenile oceanic arcs to produce granitoid magmas with enriched compositions. The Izu Collision Zone granitoid plutons provide an exceptional example of the collision-induced transformation from a juvenile oceanic arc to the mature continental crust.

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.

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.

Petrogenesis of basalts from the Archean Matachewan Dike Swarm Superior Province of Canada

NASA Technical Reports Server (NTRS)

Nelson, Dennis O.

1987-01-01

The Matachewan Dike swarm of eastern Ontario comprises Archean age basalts that were emplaced in the greenstone, granite-greenstone, and metasedimentary terrains of the Superior Province of Canada. The basalts are Fe-rich tholeiites, characterized by the near ubiquitos presence of large, compositionally uniform, calcic plagioclase. Major and trace element whole-rock compositions, along with microprobe analyses of constituent phases, from a group of dikes from the eastern portion of the province, were evaluated to constrain petrological processes that operated during the formation and evolution of the magmas. Three compositional groupings, were identified within the dikes. One group has compositional characteristics similar to modern abyssal tholeiites and is termed morb-type. A second group, enriched in incompatible elements and light-REE enriched, is referred to as the enriched group. The third more populated group has intermediate characteristics and is termed the main group. The observation of both morb-type and enriched compositions within a single dike strongly argues for the contemporaneous existence of magmas derived through different processes. Mixing calculations suggest that two possibilities exist. The least evolved basalts lie on a mixing line between the morb-type and enriched group, suggesting mixing of magmas derived from heterogeneous mantle. Mixing of magmas derived from a depleted mantle with heterogeneous Archean crust can duplicate certain aspects of the Matachewan dike composition array.

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

Petrology of peridotite xenoliths from the Miocene alkaline basalt from Baegryeong Island

NASA Astrophysics Data System (ADS)

Park, G. Y.; Kim, E.; Yang, K.

2017-12-01

Peridotite xenoliths occurring in late Miocene intraplate alkaline basalt from Baegryeong Island, west-northern part of the Korean peninsula, are mainly anhydrous spinel lherzolites. Their textures and chemical compositions give a deep insight for upper mantle. This study presents the results of modal, major composition of minerals and trace composition of clinopyroxene. The xenoliths display coarse grained protogranular through inequigranular to cumulate textures, grading into each other. They often show well-developed annealed textures and contain left-over olivine grains within orthopyroxene, suggesting that they went through static(±dynamic) recrystallization. The constituent minerals are compositionally homogeneous and appear to be equilibrated. The xenoliths are characterized by the high Mg#[=100×Mg/(Mg+Fetotal) atomic ratio] of olivine, orthopyroxene and clinopyroxene (89-93) and the Cr#[=100×Cr/(Cr+Al) atomic ratio] of spinel (9-15). The calculated equilibrium temperatures and oxygen fugacities resulted in 920-1070°C and ΔfO2 (QFM) = -1.5 -0.5, respectively. Clinopyroxenes of the xenoliths are mostly enriched in incompatible trace elements, exhibiting three types of REE patterns such as LREE-depleted, LREE-enriched and a enrichment in La over Ce, and depletion in high field strength elements(HFSE; Nb-Ta, Zr-Hf, Ti). From these trace element signatures, we thus propose the Baegryeong peridotite xenoliths represent residues left after early melt extraction, which was subsequently subjected to different degrees of modal/cryptic metasomatism by residual slab-derived, silica- and LREE-enriched fluids (or melts).

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

NASA Astrophysics Data System (ADS)

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

2005-02-01

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

Preliminary Geochemical Data for the Diabase Dykes from the Izmir-Ankara-Erzincan Suture Belt, Central Anatolia

NASA Astrophysics Data System (ADS)

Balcı, Uǧur; Sayıt, Kaan

2017-04-01

The Izmir-Ankara-Erzincan Suture Belt preserves oceanic and continental fragments originated from the closure of the northern branch of Neotethys. In the Bogazkale area (Central Anatolia), the pieces of the Neotethyan oceanic lithosphere exist in a chaotic manner, forming an ophiolitic mélange. Within the mélange, diabase dykes occur, which are found to cut various types of oceanic lithospheric rocks, including pillow basalts, gabbros and serpentinized ultramafics. We here present the preliminary geochemical results obtained from the diabase dykes and put some constraints on their petrogenesis. The investigated diabase dykes are chiefly composed of plagioclase and a mafic phase, which is clinopyroxene and/or hornblende. A detailed examination reveals two petrographic types on the basis of predominating mafic mineral phase, namely clinopyroxene-dominated Type 1, and hornblende-dominated Type 2. Ophitic to sub-ophitic textures, where lath-shaped plagioclase crystals are enclosed by clinopyroxene, can be observed in almost all Type 1 dykes. In Type 2 samples, altered mafic phases can be seen enclosed within plagioclase crystals, forming poikilitic texture. Polysynthetic twinning is common in plagioclase. Hornblende occasionally displays simple twinning. Both types appear to have been variably affected by low-grade hydrothermal alteration as reflected by the presence of secondary mineral phases, such as chlorite, epidote, prehnite, and actinolite. The whole-rock geochemistry appear to be consistent with the petrographical grouping, revealing distinct immobile trace element systematics for the two types. Both types have basaltic composition with sub-alkaline characteristics (Nb/Y=0.2-0.3 for Type 1; Nb/Y=0.02-0.08 for Type 2). The relatively low MgO contents of the dykes suggest that they do not represent primary magmas, but evolved through fractionation of mafic phases. In the N-MORB normalized diagrams, Type 2 diabases exhibit marked negative Nb anomalies, with HFSE abundances around or slightly more enriched than N-MORB. Type 1 diabases, on the other hand, do not possess any negative Nb anomalies and display enrichment in highly incompatible elements. In the chondrite-normalized diagrams, Type 1 diabases display slight LREE enrichment relative to HREE, whereas Type 2 diabases show flat to slightly LREE-depleted patterns. The N-MORB-like Nb contents of Type 2 dykes suggest that they have been derived from depleted asthenopheric mantle source. The marked enrichment of Th and La over Nb indicates that their source has been metasomatized by slab-derived fluids/melts. However, the enrichment in highly incompatible elements in Type 1 dykes implies their derivation from a relatively enriched source region and/or small degrees of partial melting. Trace element systematics suggest that Type 2 diabases may have formed in an oceanic back-arc basin environment, whereas Type 1 diabases have been generated in a mid-ocean ridge or alternatively in an oceanic back-arc basin.

Carbonatite and alkaline intrusion-related rare earth element deposits–A deposit model

USGS Publications Warehouse

Verplanck, Philip L.; Van Gosen, Bradley S.

2011-01-01

The rare earth elements are not as rare in nature as their name implies, but economic deposits with these elements are not common and few deposits have been large producers. In the past 25 years, demand for rare earth elements has increased dramatically because of their wide and diverse use in high-technology applications. Yet, presently the global production and supply of rare earth elements come from only a few sources. China produces more than 95 percent of the world's supply of rare earth elements. Because of China's decision to restrict exports of these elements, the price of rare earth elements has increased and industrial countries are concerned about supply shortages. As a result, understanding the distribution and origin of rare earth elements deposits, and identifying and quantifying our nation's rare earth elements resources have become priorities. Carbonatite and alkaline intrusive complexes, as well as their weathering products, are the primary sources of rare earth elements. The general mineral deposit model summarized here is part of an effort by the U.S. Geological Survey's Mineral Resources Program to update existing models and develop new descriptive mineral deposit models to supplement previously published models for use in mineral-resource and mineral-environmental assessments. Carbonatite and alkaline intrusion-related REE deposits are discussed together because of their spatial association, common enrichment in incompatible elements, and similarities in genesis. A wide variety of commodities have been exploited from carbonatites and alkaline igneous rocks, such as rare earth elements, niobium, phosphate, titanium, vermiculite, barite, fluorite, copper, calcite, and zirconium. Other enrichments include manganese, strontium, tantalum, thorium, vanadium, and uranium.

Mantle and crustal contributions to continental flood volcanism

USGS Publications Warehouse

Arndt, N.T.; Czamanske, G.K.; Wooden, J.L.; Fedorenko, V.A.

1993-01-01

Arndt, N.T., Czamanske, G.K., Wooden, J.L. and Fedorenko, V.A., 1993. Mantle and crustal contributions to continental flood volcanism. In: M.J.R. Wortel, U. Hansen and R. Sabadini (Editors), Relationships between Mantle Processes and Geological Processes at or near the Earth's Surface. Tectonophysics, 223: 39-52. Most continental flood basalts are enriched in incompatible elements and have high initial 87Sr/86Sr ratios and low ??{lunate}Nd values. Many are depleted in Nb and Ta. The commonly-held view that these characteristics are inherited directly from a source in metasomatized lithospheric mantle is inconsistent with the following arguments: (1) thermomechanical modelling demonstrates that flood basalt magmas come mainly from an asthenospheric or plume source, with minimal direct melting of the continental lithospheric mantle. The low water contents of most flood basalts argue against proposals that hydrous lithosphere was the source. (2) Lithospheric mantle normally has low concentrations of incompatible elements, and chondrite-normalized Nb and Ta contents similar to those of other incompatible elements. Such material cannot be the unmodified source of Nb-Ta-depleted basalts such as those from the Karoo, Ferrar, or Columbia River provinces. We suggest there are two main controls on the compositions of continental flood basalts. The first is lithospheric thickness, which strongly influences the depth and degree of mantle melting of a plume or asthenospheric source, and thus has an important influence on the composition of primary magmas. All liquids formed by partial melting of peridotite at sub-lithosphere depths are highly magnesian (20-25 wt.% MgO) but have variable trace-element contents. Where the lithosphere is thick, the source melts at high pressure, garnet is present, the degree of melting is low, and trace-element concentrations are high. This type of magma evolves to produce the high-Ti type of continental flood basalt. Where the lithosphere is thinner, the source ascends to shallower levels, the degree of melting is greater, garnet may be exhausted, and the magmas have lower trace-element contents; these magmas yield low-Ti basalts. The second control is processing of magmas in chambers that were periodically replenished and tapped, while continuously fractionating and assimilating their wall rocks. The uniform compositions of basalts that evolve in such chambers are far removed from those of their picritic parental magmas. Major elements in continental flood basalts reflect control by olivine, pyroxene, and plagioclase crystallization, and this assemblage places the magma chambers at crustal depth. We believe that trace-element and isotopic compositions are also buffered, and that the erupted basalts represent steady-state liquids tapped from these magma chambers. These processes impose a crustal signature on the magmas, as expressed most strongly in the concentrations of incompatible elements (e.g., Nb-Ta anomalies) and their isotopic characteristics. ?? 1993.

Geochemistry of carbonatites of the Tomtor massif

USGS Publications Warehouse

Kravchenko, S.M.; Czamanske, G.; Fedorenko, V.A.

2003-01-01

Carbonatites compose sheet bodies in a 300-m sequence of volcanic lamproites, as well as separate large bodies at depths of >250-300 m. An analysis of new high-precision data on concentrations of major, rare, and rare earth elements in carbonatites shows that these rocks were formed during crystallization differentiation of a carbonatite magma, which resulted in enrichment of the later melt fractions in rare elements and was followed by autometasomatic and allometasomatic hydrothermal processes. Some independent data indicate that the main factor of ore accumulation in the weathered rock zone (also known as the "lower ore horizon" comprising metasomatized volcanics with interbedded carbonatites) was hydrothermal addition of Nb and REEs. The giant size of the Tomtor carbonatite-nepheline syenite massif caused advanced magma differentiation, extensive postmagmatic metasomatism and recrystallization of host rocks, and strong enrichment of carbonatites in incompatible rare and rare earth elements (except for Ta, Zr, Ti, K, and Rb) compared to the rocks of many other carbonatite massifs. We suggest that a wide range of iron contents in carbonatites-2 can be related to extensive magnetite fractionation at the magmatic stage in different parts of the huge massif. Copyright ?? 2003 by MAIK "Nauka/Interperiodica" (Russia).

Chemical signature of a migrating grain boundaries in polycrystalline olivine

NASA Astrophysics Data System (ADS)

Boneh, Y.; Marquardt, K.; Skemer, P. A.

2017-12-01

Olivine is the most abundant phase and influences strongly the physical and chemical properties of the upper mantle. The structure and chemistry of olivine grain-boundaries is important to understand, as these interfaces provide a reservoir for incompatible elements and partial melt, and serve as a fast pathway for chemical diffusion. This project investigates the chemical characteristics of grain boundaries in an olivine-rich aggregate. The sample is composed of Fo50 olivine crystals with minor amounts of enstatite. It was previously deformed (Hansen et al., 2016) and then annealed (Boneh et al., 2017) to investigate the microstructural changes during recrystallization. This transient microstructure has a bimodal grain size distribution and includes grains that experienced abnormal grain-growth, (porphyroblasts) and highly strained grains with no significant recrystallization or growth (matrix). Using high-resolution transmission electron microscopy (HR-TEM) with energy dispersive X-ray (EDX) at the Bayerisches Geoinstitut (BGI), we characterized boundaries between pairs of porphyroblasts, pairs of matrix grains, and mixed boundaries between porphyroblast and matrix grains. It was found that the boundary between porphyroblasts is enriched in Al and Ca and depleted in Mg, in comparison to grain interiors. However, matrix-matrix boundaries show less chemical segregation of these elements. The relatively high level of chemical segregation to porphyroblast grain boundaries offers different possible interpretations: 1) During grain boundary migration incompatible elements are swept up by the migrating grain boundary. 2) Large angle grain boundaries provide a large density of energetically favorable storage sites for incompatible elements. 3) Diffusion along low angle grain boundaries is too slow to allow for fast chemical equilibration between the different grain boundaries. 4) Dislocations cores serve as an important transport media for impurities (i.e., Cottrell atmosphere). We will further discuss these different interpretations, their feasibility, and implications for the geochemistry of the mantle.

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

NASA Astrophysics Data System (ADS)

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

2016-03-01

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

Northwest Africa 773: Lunar Mare Breccia with a Shallow-formed Olivine-Cumulate Component, Very-Low-Ti Heritage, and a KREEP Connection

NASA Technical Reports Server (NTRS)

Jolliff, B. L.; Korotev, R. L.; Zeigler, R. A.; Floss, C.; Haskin, L. A.

2003-01-01

Northwest Africa 773 is one of the more unusual lunar meteorites found in recent years because it contains a prominent clast lithology, which appears to be an olivine-rich cumulate and because it is a very-low-Ti (VLT) mare breccia with relatively high incompatible-trace-element concentrations and LREE/HREE enrichment. A lunar origin was verified by Fagan and coworkers on the basis of noble-gas contents, oxygen isotopes, and mineral compositions. Fagan et al. described two lithologies: (1) heterolithic impact breccia with a regolith component and (2) cumulus olivine gabbronorite. Here, we refer to these as the breccia (Bx) lithology and the olivine-cumulate (OC) lithology. The impact breccia components are predominantly volcanic (basaltic), and, in this context, the occurrence of the cumulus lithology is especially significant: is it related to the volcanic components or does it represent a deep-seated rock entrained by the basaltic magma as it rose to the surface? Elevated incompatible-element concentrations with more or less KREEP-like inter-element ratios and very-low-Ti concentrations distinguish both lithologies of this meteorite from Apollo mare basalts. Here, we summarize key compositional information (bulk and mineral), especially related to the OC lithology, to show that it formed at shallow depth and comes from a VLT ultramafic precursor that mixed with a KREEP-like trace-element component deep in the crust or upper mantle.

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.

Mesoarchean melting and Neoarchean to Paleoproterozoic metasomatism during the formation of the cratonic mantle keel beneath West Greenland

NASA Astrophysics Data System (ADS)

van Acken, D.; Luguet, A.; Pearson, D. G.; Nowell, G. M.; Fonseca, R. O. C.; Nagel, T. J.; Schulz, T.

2017-04-01

Highly siderophile element (HSE) concentration and 187Os/188Os isotopic heterogeneity has been observed on various scales in the Earth's mantle. Interaction of residual mantle peridotite with infiltrating melts has been suggested to overprint primary bulk rock HSE signatures originating from partial melting, contributing to the heterogeneity seen in the global peridotite database. Here we present a detailed study of harzburgitic xenolith 474527 from the Kangerlussuaq suite, West Greenland, coupling the Re-Os isotope geochemistry with petrography of both base metal sulfides (BMS) and silicates to assess the impact of overprint induced by melt-rock reaction on the Re-Os isotope system. Garnet harzburgite sample 474527 shows considerable heterogeneity in the composition of its major phases, most notably olivine and Cr-rich garnet, suggesting formation through multiple stages of partial melting and subsequent metasomatic events. The major BMS phases show a fairly homogeneous pentlandite-rich composition typical for BMS formed via metasomatic reaction, whereas the 187Os/188Os compositions determined for 17 of these BMS are extremely heterogeneous ranging between 0.1037 and 0.1981. Analyses by LA-ICP-MS reveal at least two populations of BMS grains characterized by contrasting HSE patterns. One type of pattern is strongly enriched in the more compatible HSE Os, Ir, and Ru over the typically incompatible Pt, Pd, and Re, while the other type shows moderate enrichment of the more incompatible HSE and has overall lower compatible HSE/incompatible HSE composition. The small-scale heterogeneity observed in these BMS highlights the need for caution when utilizing the Re-Os system to date mantle events, as even depleted harzburgite samples such as 474527 are likely to have experienced a complex history of metasomatic overprinting, with uncertain effects on the HSE.

Alkalic Lavas From Nintoku Seamount, Emperor Seamount Chain: Geochemistry of Hawaiian Post-Shield Magmatism at 55 Ma

NASA Astrophysics Data System (ADS)

Shafer, J. T.; Gudding, J. A.; Neal, C. R.; Regelous, M.

2002-12-01

Ocean Drilling Project (ODP) Leg 197, Site 1205 penetrated 283 m into the volcanic basement of Nintoku Seamount, which is located roughly half-way along the Emperor Seamount Chain and has been dated at approximately 55-56 Ma by 40Ar-39Ar (R. Duncan, pers. comm., 2002). 25 subaerially-erupted lava flows, together with interflow sediments and soil horizons, were recovered. We report major and trace element compositions of 33 rock samples spanning the entire lava sequence and hawaiite clasts from a conglomerate immediately overlying the igneous basement. The volcanic rocks at Site 1205 are dominantly alkalic to intermediate basalts with between 5 and 11% MgO, with the degree of alkalinity generally increasing up-section, and the eruption rate (inferred from the thickness and abundance of interflow soils) appears to have decreased with time. Two flows in the lower half of the hole are tholeiitic and divide the section into two different alkalic basalt series. One of these flows contains accumulated olivine crystals and has a picritic composition. The upper alkalic series generally becomes enriched in the highly incompatible elements (ITEs) up-section from the tholeiitic units and is overlain by a conglomerate that contains cobbles of hawaiite that are highly enriched in ITEs. Normalized patterns are subparallel to those of the upper series of alkalic basalts, suggesting the hawaiites may be related by fractional crystallization. The lower alkalic series contains basalts that are among the most ITE enriched of the recovered basement sequence, but does not show the same variations as the upper series. The petrology of the Site 1205 lavas is very similar to those of lavas erupted during the later evolutionary stages of young volcanoes from the Hawaiian Islands and were probably all erupted during the post-shield alkalic stage; at Nintoku the post-shield alkalic cap appears to be relatively thick (at least 300m) compared to many other Hawaiian volcanoes, but is similar to that of Mauna Kea and Haleakala. Fractionation of the observed phenocryst phases (olivine and plagioclase) was responsible for much of the compositional variation within the Nintoku basaltic lavas, and the low Sc concentrations of the hawaiites show that they have also fractionated clinopyroxene. However, variations in incompatible trace element ratios indicate that the lavas cannot all be related by crystal fractionation from a single parental magma. Nintoku lavas exhibit broad similarities in major and trace element compositions of post-shield lavas from the Hawaiian Islands. For example, La/Yb ratios of the 1205 basalts (5-13) are similar to those of alkali basalts from Mauna Kea (5-12), but lower than those from Haleakala (12-17). However, distinct differences also occur. Nintoku lavas have relatively low Zr concentrations, so that they plot below the main Hawaiian array on a Zr/Nb-La/Yb diagram. Previous studies have show that lavas from the oldest Emperor Seamounts have relatively depleted incompatible trace element compositions; our data suggest that by 56 Ma, lavas erupted above the Hawaiian Hotspot were essentially similar to young (<5 Ma) lavas from the Hawaiian Islands.

Rare Mineralogy in Alkaline Ultramafic Rocks, Western Kentucky Fluorspar District

NASA Astrophysics Data System (ADS)

Anderson, W.

2017-12-01

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

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.

Geochemistry of pillow lavas and sheeted dikes from Nain and Ashin ophiolites (Central Iran)

NASA Astrophysics Data System (ADS)

Saccani, Emilio; Pirnia Naeini, Tahmineh; Torabi, Ghodrat

2017-04-01

An extensive, worldwide database on the geochemistry of basalts from well-known tectonic settings is available. Knowing the chemistry of basalts on one hand, and the tectonic setting of their origin on the other hand, resulted in the development of tectonic discrimination diagrams. Recently developed discrimination diagrams allow us to determine the tectonic setting of volcanics with almost neglectable probability of misclassification (<1%). One major application of these diagrams lies in discriminating the tectonic setting of formation of ophiolites, particularly in poorly-known areas. A good example is the Inner ophiolite belt of Iran, located in Central Iran. The geodynamic significance of the inner ophiolites is still poorly known. From the Inner ophiolites, either no volcanic section is reported, or, the data are highly limited and poorly-reliable due the high degree of alteration of the studied samples. We have been able to overcome this problem by spotting relatively well-preserved outcrops of pillow lavas and sheeted dikes from two ophiolite mélanges of Central Iran, Nain and Ashin ophiolites. The two mélanges are located in the west of Central-East Iranian microplate. In total, 28 samples have been collected from the pillow lavas and sheeted dikes outcrops. The studied volcanic rocks consist mainly of basalts and minor ferrobasalts and basaltic andesites, all showing a clear subalkaline nature (e.g., Nb/Y = 0.03-0.21). Two samples from the Nain ophiolite are characterized by N-MORB normalized incompatible element patterns showing marked Th positive anomalies and Ta, Nb, Ti negative anomalies. Chondrite-normalized REE patterns show LREE/HREE (light REE/heavy REE) enrichment, with LaN/YbN=3.2-4.3. These rocks are chemically similar to the calc-alkaline basalts (CAB), as also highlighted by many discrimination diagrams. These rocks are interpreted to have generated in a cordilleran-type volcanic arc setting. All other samples from both the Nain and Ashin ophiolites display a wide range of chemical composition. However, the relatively less fractionated basalts are characterized by low TiO2 (0.60-1 wt%), P2O5 (0.03-0.08 wt%), Zr (23-75 ppm) and Y (9-27) contents. Cr (38-619 ppm) and Ni (22-220 ppm) contents show a wide range of variation. N-MORB normalized incompatible element patterns show rather flat trends and a general depletion (from 0.4 to 0.8 times N-MORB composition) coupled with a slight Th enrichment (1-3 times N-MORB). Chondrite-normalized REE patterns are generally flat and are characterized by either a slight depletion or a slight enrichment in LREE compared to HREE (LaN/YbN=0.7-1.2). These overall chemical features resemble those of island arc tholeiites from many ophiolitic complexes. The depletion in incompatible elements compared to N-MORB suggest that these rocks were derived from partial melting of a depleted mantle source. Th enrichment with respect to Nb (ThN/NbN = 2.6-12.4) suggests that mantle sources underwent enrichment in subduction-derived chemical components prior melting. Our data suggest that the Nain and Ashin ophiolites were formed in a subduction-related tectonic setting during the Late Cretaceous. The chemistry of the studied rocks is compatible with transition zone either from forearc to arc or from arc to backarc.

Geochemistry of post-spreading lavas from fossil Mathematician and Galapagos spreading axes, revisited

NASA Astrophysics Data System (ADS)

Tian, L.; Castillo, P. R.; Hilton, D. R.

2010-12-01

The Mathematician Ridge, located west of the northern end of the EPR at about 10-20°N, 110°W, was abandoned during the Pliocene when the Pacific plate captured the Mathematician microplate. The Galapagos Rise, located east of the southern segment of the EPR at about 10-18°S, 95°W, ceased spreading after the Late Miocene capture of the Bauer microplate by the Nazca plate. Here we report new major and trace element and Sr, Nd and Pb isotope data for lavas dredged from seamounts and volcanic ridges along the crest of Mathematician Ridge [Batiza and Vanko, J. Petrol. 26, 1985] and from narrow volcanic ridges built along extinct segments of the Galapagos Rise [Batiza et al., Mar. Geol. 49, 1982]. These lavas consist predominantly of alkalic basalts and their differentiates, similar to the post-spreading alkalic lava series in other fossil spreading axes (e.g., Davidson Seamount, Guide Seamount, Socorro Island, and fossil spreading axes off Baja California Sur) and alkalic lavas from near-ridge seamounts in the eastern Pacific [Castillo et al., G3 11, 2010; Tian et al., sub. to G3]. Collectively, the alkalic lavas have higher incompatible trace element contents and highly/moderately incompatible trace element ratios (e.g., Ba/Zr >1.3, La/Sm >2.7 and Nb/Zr >0.14) than EPR basalts, and are similar to average alkalic OIB. They also have similar 87Sr/86Sr (0.7027 - 0.7037), 143Nd/144Nd (0.51289 - 0.51306) and 206Pb/204Pb (18.70 - 19.84) compositions, which overlap with geochemically enriched (E-) MORB and ~depleted OIB from major hotspot volcanic chains such as Galapagos, Hawaii and Iceland. The new data suggest that intraplate lavas from fossil spreading axes and non-hotspot seamounts in the eastern Pacific share a common enriched source which is geographically dispersed in the upper mantle.

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.

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.

Geochemistry of Martian Meteorites and the Petrologic Evolution of Mars

NASA Technical Reports Server (NTRS)

Mittlefehldt, D. W.

2002-01-01

Mafic igneous rocks serve as probes of the interiors of their parent bodies - the compositions of the magmas contain an imprint of the source region composition and mineralogy, the melting and crystallization processes, and mixing and assimilation. Although complicated by their multifarious history, it is possible to constrain the petrologic evolution of an igneous province through compositional study of the rocks. Incompatible trace elements provide one means of doing this. I will use incompatible element ratios of martian meteorites to constrain the early petrologic evolution of Mars. Incompatible elements are strongly partitioned into the melt phase during igneous processes. The degree of incompatibility will differ depending on the mineral phases in equilibrium with the melt. Most martian meteorites contain some cumulus grains, but nevertheless, incompatible element ratios of bulk meteorites will be close to those of their parent magmas. ALH 84001 is an exception, and it will not be discussed. The martian meteorites will be considered in two groups; a 1.3 Ga group composed of the clinopyroxenites and dunite, and a younger group composed of all others.

Volatile abundances and oxygen isotopes in basaltic to dacitic lavas on mid-ocean ridges: The role of assimilation at spreading centers

USGS Publications Warehouse

Wanless, V.D.; Perfit, M.R.; Ridley, W.I.; Wallace, P.J.; Grimes, Craig B.; Klein, E.M.

2011-01-01

Most geochemical variability in MOR basalts is consistent with low- to moderate-pressure fractional crystallization of various mantle-derived parental melts. However, our geochemical data from MOR high-silica glasses, including new volatile and oxygen isotope data, suggest that assimilation of altered crustal material plays a significant role in the petrogenesis of dacites and may be important in the formation of basaltic lavas at MOR in general. MOR high-silica andesites and dacites from diverse areas show remarkably similar major element trends, incompatible trace element enrichments, and isotopic signatures suggesting similar processes control their chemistry. In particular, very high Cl and elevated H2O concentrations and relatively light oxygen isotope ratios (~ 5.8‰ vs. expected values of ~ 6.8‰) in fresh dacite glasses can be explained by contamination of magmas from a component of ocean crust altered by hydrothermal fluids. Crystallization of silicate phases and Fe-oxides causes an increase in δ18O in residual magma, but assimilation of material initially altered at high temperatures results in lower δ18O values. The observed geochemical signatures can be explained by extreme fractional crystallization of a MOR basalt parent combined with partial melting and assimilation (AFC) of amphibole-bearing altered oceanic crust. The MOR dacitic lavas do not appear to be simply the extrusive equivalent of oceanic plagiogranites. The combination of partial melting and assimilation produces a distinct geochemical signature that includes higher incompatible trace element abundances and distinct trace element ratios relative to those observed in plagiogranites.

Geochemistry of lavas from the Australian-Antarctic Ridge, easternmost Southeast Indian Ridge

NASA Astrophysics Data System (ADS)

Park, S.; Langmuir, C. H.; Lin, J.; Kim, S.; Hahm, D.; Michael, P. J.; Baker, E. T.

2012-12-01

The intermediate spreading Australian-Antarctic Ridge (AAR), an easternmost extension of the South East Indian Ridge located in the south of Tasmania, is one of the largest unexplored regions of the global mid-ocean ridge system, owing to its remote location and a very limited workable weather window. In early and late 2011, the Korea Polar Research Institute (KOPRI) conducted two surveys of two segments at 160°E (KR1) and 152.5°E (KR2) using the icebreaker Araon, producing a multi-beam map, 48 rock core samples and a MAPR (Miniature Autonomous Plume Recorder) hydrothermal survey. The full spreading rate of the spreading center in this area is 68 mm/yr. The axial depth of KR1 is relatively shallow (~2,000m) and is a first-order segment bounded by two large offset transform faults. The axial morphology of KR1 varies substantially from an axial high plateau (Segment 1) in the west, to a small rift valley (Segment 2), to an axial high with graben (Segment 3), and to a substantial rift valley (Segment 4) in the east. These changes occur in the absence of marked offsets in the ridge, such as overlapping spreading centers. Even so, these segments can be divided still further into shorter scale segments based on small discontinuities in the linearity of the axis and variations in rock chemistry. Small offsets in bathymetry can be associated with large chemical changes, such as between Segments 2 and 3, where incompatible element abundances change by almost a factor of ten. Incompatible trace element ratios for basalts show a regular pattern that is nonetheless not a single gradient. Along Segments 1 and 2, an axial high changes to a modest rift, (La/Sm)N of basalts decreases from 0.9 to 0.5. Then there is an abrupt step in enrichment to (La/Sm)N of 1.5, associated with a shallower depths and the appearance of an off-axis seamount south of the axis. This enrichment persists eastwards and then declines progressively to values of (La/Sm)N of 0.7 in the pronounced rift valley of Segment 4. Plume signals indicating hydrothermal vents were found in the middle of KR1 where the most enriched basalts occur and the magma supply appears robust. The first- order segment KR2 can be divided into two segments -- an axial high western segment, and a rift valley eastern segment. Hydrothermal vent signals were mainly found in the western part of the segment. The KR2 samples are mostly depleted, but KR2 also contains enriched basalts, including an E-MORB with 0.65% K2O in the western segment. Enriched KR2 basalts have different ratios of alkalis to HFSE compared to KR1, suggesting they are not derived from the same enriched component. In general in this region, inflated axial morphology is associated with trace element enrichment, suggesting that magma flux is being influenced by changing mantle composition on the segment scale.

Rethinking Recycling in Arcs

NASA Astrophysics Data System (ADS)

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

2012-12-01

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

Platinum-group element, Gold, Silver and Base Metal distribution in compositionally zoned sulfide droplets from the Medvezky Creek Mine, Noril'sk, Russia

USGS Publications Warehouse

Barnes, S.-J.; Cox, R.A.; Zientek, M.L.

2006-01-01

Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril'sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into pentlandite. ?? Springer-Verlag 2006.

Stratigraphic and geochemical evolution of an oceanic arc upper crustal section: The Jurassic Talkeetna Volcanic Formation, south-central Alaska

USGS Publications Warehouse

Clift, P.D.; Draut, A.E.; Kelemen, P.B.; Blusztajn, J.; Greene, A.

2005-01-01

The Early Jurassic Talkeetna Volcanic Formation forms the upper stratigraphic level of an oceanic volcanic arc complex within the Peninsular Terrane of south-central Alaska. The section comprises a series of lavas, tuffs, and volcaniclastic debris-How and flow turbidite deposits, showing significant lateral facies variability. There is a general trend toward more volcaniclastic sediment at the top of the section and more lavas and tuff breccias toward the base. Evidence for dominant submarine, mostly mid-bathyal or deeper (>500 m) emplacement is seen throughout the section, which totals ???7 km in thickness, similar to modern western Pacific arcs, and far more than any other known exposed section. Subaerial sedimentation was rare but occurred over short intervals in the middle of the section. The Talkeetna Volcanic Formation is dominantly calc-alkatine and shows no clear trend to increasing SiO2 up-section. An oceanic subduction petrogenesis is shown by trace element and Nd isotope data. Rocks at the base of the section show no relative enrichment of light rare earth elements (LREEs) versus heavy rare earth elements (REES) or in melt-incompatible versus compatible high field strength elements (HFSEs). Relative enrichment of LREEs and HFSEs increases slightly up-section. The Talkeetna Volcanic Formation is typically more REE depleted than average continental crust, although small volumes of light REE-enriched and heavy REE-depleted mafic lavas are recognized low in the stratigraphy. The Talkeetna Volcanic Formation was formed in an intraoceanic arc above a north-dipping subduction zone and contains no preserved record of its subsequent collisions with Wrangellia or North America. ?? 2005 Geological Society of America.

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

NASA Astrophysics Data System (ADS)

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

2015-05-01

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

Modelling the isotopic evolution of the Earth.

PubMed

Paul, Debajyoti; White, William M; Turcotte, Donald L

2002-11-15

We present a flexible multi-reservoir (primitive lower mantle, depleted upper mantle, upper continental crust, lower continental crust and atmosphere) forward-transport model of the Earth, incorporating the Sm-Nd, Rb-Sr, U-Th-Pb-He and K-Ar isotope-decay systematics. Mathematically, the model consists of a series of differential equations, describing the changing abundance of each nuclide in each reservoir, which are solved repeatedly over the history of the Earth. Fluxes between reservoirs are keyed to heat production and further constrained by estimates of present-day fluxes (e.g. subduction, plume flux) and current sizes of reservoirs. Elemental transport is tied to these fluxes through 'enrichment factors', which allow for fractionation between species. A principal goal of the model is to reproduce the Pb-isotope systematics of the depleted upper mantle, which has not been done in earlier models. At present, the depleted upper mantle has low (238)U/(204)Pb (mu) and (232)Th/(238)U (kappa) ratios, but Pb-isotope ratios reflect high time-integrated values of these ratios. These features are reproduced in the model and are a consequence of preferential subduction of U and of radiogenic Pb from the upper continental crust into the depleted upper mantle. At the same time, the model reproduces the observed Sr-, Nd-, Ar- and He-isotope ratios of the atmosphere, continental crust and mantle. We show that both steady-state and time-variant concentrations of incompatible-element concentrations and ratios in the continental crust and upper mantle are possible. Indeed, in some cases, incompatible-element concentrations and ratios increase with time in the depleted mantle. Hence, assumptions of a progressively depleting or steady-state upper mantle are not justified. A ubiquitous feature of this model, as well as other evolutionary models, is early rapid depletion of the upper mantle in highly incompatible elements; hence, a near-chondritic Th/U ratio in the upper mantle throughout the Archean is unlikely. The model also suggests that the optimal value of the bulk silicate Earth's K/U ratio is close to 10000; lower values suggested recently seem unlikely.

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

NASA Astrophysics Data System (ADS)

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

2017-10-01

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

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

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

NASA Astrophysics Data System (ADS)

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

2013-04-01

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

Chondritic late accretion to Mars and the nature of shergottite reservoirs

NASA Astrophysics Data System (ADS)

Tait, Kim T.; Day, James M. D.

2018-07-01

Mars is considered to have formed as a planetary embryo that experienced extensive differentiation early in its history. Shergottite meteorites preserve evidence for this history, and for late accretion events that affected their mantle sources within Mars. Here we report the first coupled 187Re-187Os, 87Sr/86Sr, highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, Re) and major element abundance dataset for martian shergottites that span a range of MgO contents, from 6.4 to 30.3 wt.%. The shergottites range from picro-basalt to basaltic-andesite compositions, have enriched to depleted incompatible trace-element compositions, and define fractional crystallization trends, enabling the determination of HSE compatibility for martian magmatism in the order: Os > Ir ≥ Ru ≫ Pt ≥ Pd ≥ Re. This order of compatibility is like that defined previously for Earth and the Moon, but the fractionation of strongly compatible Os, Ir and Ru appears to take place at higher MgO contents in martian magmas, due to early onset of sulfide fractionation. In general, enriched shergottites have lower MgO contents than intermediate or depleted shergottites and have fractionated HSE patterns (Re + Pd + Pt > Ru + Ir + Os) and more radiogenic measured 87Sr/86Sr (0.7127-0.7235) and 187Os/188Os (0.140-0.247) than intermediate or depleted shergottite meteorites (87Sr/86Sr = 0.7010-0.7132; 187Os/188Os = 0.127-0.141). Osmium isotope compositions, corrected for crystallization age, define compositions that are implausibly unradiogenic in some enriched shergottites, implying recent mobilization of Re in some samples. Filtering for the effects of alteration and high Re/Os through crystal-liquid fractionation leads to a positive correlation between age-corrected Sr and Os isotope compositions. Mixing between hypothetical martian crustal and mantle reservoirs are unable to generate the observed Sr-Os isotope compositions of shergottites, which require either distinct and discrete long-term incompatible-element depleted and enriched mantle sources, or originate from hybridized melting of deep melts with metasomatized martian lithosphere. Using MgO-regression methods, we obtain a modified estimate of the bulk silicate Mars HSE composition of (in ng g-1) 0.4 [Re], 7.4 [Pd], 9.6 [Pt], 6.2 [Ru], 3.7 [Ir], 4 [Os], and a long-term chondritic 187Os/188Os ratio (∼0.1312). This result does not permit existing models invoking high-pressure and temperature partitioning of the HSE. Instead, our estimate implies 0.6-0.7% by mass of late accretion of broadly chondritic material to Mars. Our results indicate that Mars could have accreted earlier than Earth, but that disproportional accretion of large bodies and a relative constant flux of accretion of available materials in the first 50-100 Ma of Solar System led to the broad similarity in HSE abundances between Earth and Mars.

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-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.

A Dual-Porosity, In Situ Crystallisation Model For Fast-Spreading Mid-Ocean Ridge Magma Chambers Based Upon Direct Observation From Hess Deep

NASA Astrophysics Data System (ADS)

MacLeod, C. J.; Lissenberg, C. J.

2014-12-01

We propose a revised magma chamber model for fast-spreading mid-ocean ridges based upon a synthesis of new data from a complete section of lower crust from the East Pacific Rise, reconstructed from samples collected from the Hess Deep rift valley during cruise JC21. Our investigation includes detailed sampling across critical transitions in the upper part of the plutonic section, including the inferred axial melt lens (AML) within the dyke-gabbro transition. We find that an overall petrological progression, from troctolite and primitive gabbro at the base up into evolved (oxide) gabbro and gabbronorite at the top of the lower crustal section, is mirrored by a progressive upward chemical fractionation as recorded in bulk rock and mineral compositions. Crystallographic preferred orientations measured using EBSD show that the downward increase in deformation of mush required in crystal subsidence models is not observed. Together these observations are consistent only with a model in which crystallisation of upward migrating evolving melts occurs in situ in the lower crust. Over-enrichment in incompatible trace element concentrations and ratios above that possible by fractional crystallisation is ubiquitous. This implies redistribution of incompatible trace elements in the lower crust by low porosity, near-pervasive reactive porous flow of interstitial melt moving continuously upward through the mush pile. Mass balance calculations reveal a significant proportion of this trace element enriched melt is trapped at mid-crustal levels. Mineral compositions in the upper third to half of the plutonic section are too evolved to represent the crystal residues of MORB. Erupted MORB therefore must be fed from melts sourced in the deeper part of the crystal mush pile, and which must ascend rapidly without significant modification in the upper plutonics or AML. From physical models of mush processes we posit that primitive melts are transported through transient, high porosity channels generated by gravitational instabilities that periodically overturn and drain crystallising melt bodies (sills) from deeper levels of the lower crustal mush. We conclude that magma chambers are characterised by melt delivery to the deep crust, followed by in situ crystallisation of melts transported upwards via a dual-porosity system.

Constraints on the Parental Melts of Enriched Shergottites from Image Analysis and High Pressure Experiments

NASA Technical Reports Server (NTRS)

Collinet, M.; Medard, E.; Devouard, B.; Peslier, A.

2012-01-01

Martian basalts can be classified in at least two geochemically different families: enriched and depleted shergottites. Enriched shergottites are characterized by higher incompatible element concentrations and initial Sr-87/Sr-86 and lower initial Nd-143/Nd-144 and Hf-176/Hf-177 than depleted shergottites [e.g. 1, 2]. It is now generally admitted that shergottites result from the melting of at least two distinct mantle reservoirs [e.g. 2, 3]. Some of the olivine-phyric shergottites (either depleted or enriched), the most magnesian Martian basalts, could represent primitive melts, which are of considerable interest to constrain mantle sources. Two depleted olivine-phyric shergottites, Yamato (Y) 980459 and Northwest Africa (NWA) 5789, are in equilibrium with their most magnesian olivine (Fig. 1) and their bulk rock compositions are inferred to represent primitive melts [4, 5]. Larkman Nunatak (LAR) 06319 [3, 6, 7] and NWA 1068 [8], the most magnesian enriched basalts, have bulk Mg# that are too high to be in equilibrium with their olivine megacryst cores. Parental melt compositions have been estimated by subtracting the most magnesian olivine from the bulk rock composition, assuming that olivine megacrysts have partially accumulated [3, 9]. However, because this technique does not account for the actual petrography of these meteorites, we used image analysis to study these rocks history, reconstruct their parent magma and understand the nature of olivine megacrysts.

R-process enrichment from a single event in an ancient dwarf galaxy.

PubMed

Ji, Alexander P; Frebel, Anna; Chiti, Anirudh; Simon, Joshua D

2016-03-31

Elements heavier than zinc are synthesized through the rapid (r) and slow (s) neutron-capture processes. The main site of production of the r-process elements (such as europium) has been debated for nearly 60 years. Initial studies of trends in chemical abundances in old Milky Way halo stars suggested that these elements are produced continually, in sites such as core-collapse supernovae. But evidence from the local Universe favours the idea that r-process production occurs mainly during rare events, such as neutron star mergers. The appearance of a plateau of europium abundance in some dwarf spheroidal galaxies has been suggested as evidence for rare r-process enrichment in the early Universe, but only under the assumption that no gas accretes into those dwarf galaxies; gas accretion favours continual r-process enrichment in these systems. Furthermore, the universal r-process pattern has not been cleanly identified in dwarf spheroidals. The smaller, chemically simpler, and more ancient ultrafaint dwarf galaxies assembled shortly after the first stars formed, and are ideal systems with which to study nucleosynthesis events such as the r-process. Reticulum II is one such galaxy. The abundances of non-neutron-capture elements in this galaxy (and others like it) are similar to those in other old stars. Here, we report that seven of the nine brightest stars in Reticulum II, observed with high-resolution spectroscopy, show strong enhancements in heavy neutron-capture elements, with abundances that follow the universal r-process pattern beyond barium. The enhancement seen in this 'r-process galaxy' is two to three orders of magnitude higher than that detected in any other ultrafaint dwarf galaxy. This implies that a single, rare event produced the r-process material in Reticulum II. The r-process yield and event rate are incompatible with the source being ordinary core-collapse supernovae, but consistent with other possible sources, such as neutron star mergers.

The Paradox of the Axial Melt Lens: Petrology and Geochemistry of the Upper Plutonics at Hess Deep

NASA Astrophysics Data System (ADS)

Lissenberg, C. J.; Loocke, M. P.; MacLeod, C. J.

2014-12-01

The axial melt lens (AML) is a steady-state magma-rich body located at the dyke-gabbro transition at intermediate- and fast-spreading ridges. It is widely believed to be the reservoir from which mid-ocean ridge basalt (MORB) is erupted. The paradox of the axial melt lens is that the plutonic rocks that occur at this level are far too evolved to be in equilibrium with MORB, which is basaltic by definition; hence, the plutonic and volcanic records do not match. We explore this paradox by study of the first comprehensive sample suite of the uppermost plutonics of a fast-spreading ridge, taken by remotely-operated vehicle from the Hess Deep rift during cruise JC21. 23 samples (8 dolerites, 14 gabbronorites, and 1 gabbro) were collected from a section containing the transition from the uppermost gabbroic section into sheeted dykes. We present the results of a detailed petrographic and microanalytical investigation of these samples. They are dominated by evolved, varitextured (both in hand sample and thin section) oxide gabbronorites; olivine occurs in only one sample. A preponderance of the samples have positive Eu/Eu* and Sr/Sr*, indicating a cumulate origin. However, the minerals have evolved compositions, and are in equilibrium with melts significantly more evolved than East Pacific Rise MORB. Furthermore, the trace element contents of clinopyroxene differ significantly from clinopyroxene in equilibrium with MORB, being more enriched in incompatible elements. To account for both the evidence of derivation of MORB from the AML and the evolved nature of its rock record, we posit that the AML must be fed by melts on two different timescales: continual low-volume feeding by evolved interstitial melt from the cumulus pile below is augmented episodically by delivery of high volumes of more primitive melt. The latter episodes may trigger eruptions; hence the primitive melts are held in the magma chamber for only short periods, and erupt on the seafloor before significant crystallisation in the AML has taken place. This model for the feeding of the AML provides ample opportunity for mixing between the relatively primitive melts and the evolved, trace-element-rich melt, and accounts for the observed over-enrichment in incompatible elements of MORB.

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

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.

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.

Mineralogy and composition of the oceanic mantle

USGS Publications Warehouse

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

2011-01-01

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

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

NASA Astrophysics Data System (ADS)

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

2015-12-01

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

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.

K/TH in Achondrites and Interpretation of Grand Data for the Dawn Mission

NASA Technical Reports Server (NTRS)

Usui, T.; McSween, H. Y., Jr.; Mittlefehldt, D. W.; Prettyman, T. H.

2008-01-01

The Dawn mission will explore 4 Vesta [1], a highly differentiated asteroid believed to be the parent body of the howardite, eucrite and diogenite (HED) meteorite suite [e.g. 2]. The Dawn spacecraft is equipped with a gamma-ray and neutron detector (GRaND), which will enable measurement and mapping of elemental abundances on Vesta s surface [3]. Drawing on HED geochemistry, Usui and McSween [4] proposed a linear mixing model for interpretation of GRaND data. However, the HED suite is not the only achondrite suite representing asteroidal basaltic crusts; others include the mesosiderites, angrites, NWA 011, and possibly Ibitira, each of which is thought to have a distinct parental asteroid [5]. Here we critically examine the variability of GRaND-analyzed elements, K and Th, in HED meteorites, and propose a method based on the K-Th systematics to distinguish between HED and the other differentiated achondrites. Maps of these elements might also recognize incompatible element enriched areas such as mapped locally on the Moon (KREEP) [6], and variations in K/Th ratios might indicate impact volatilization of K. We also propose a new mixing model using elements that will be most reliably measured by GRaND, including K.

Hemispheric dichotomy in lithosphere growth on Mars caused by differences in crustal composition

NASA Astrophysics Data System (ADS)

Thiriet, M.; Michaut, C.; Breuer, D.

2016-12-01

The surface dichotomy is the most striking feature of Mars. The Northern hemisphere is covered by extensive lava plains and is lower in altitude than the South which has higher and sharper reliefs and is more craterized and older than the North. Recent studies have suggested that this bimodal distribution of altitudes could be due to the existence of a buried felsic component similar to the terrestrial continental crust in the Southern hemisphere. The presence of a large buried component of evolved composition might imply an enrichment in incompatible radioactive elements. The thermal surface properties of the two hemispheres also seem to differ; the South shows fine-particulate materials probably resulting from explosive volcanism, while the Northern lava flows are more consolidated and characterized by a higher thermal conductivity. Using a parameterized convection model with a stagnant lid, we computed the thermal evolution and lithosphere growth of Mars accounting for potential differences in the thermal parameters characterizing the Northern and Southern crusts. We find that a stronger enrichment in radioactive elements and a lower surface conductivity in the South can cause a significant difference in elastic thickness of the lithosphere in between both hemispheres, with an elastic lithosphere thicker in the North by several tens of kilometers today. This result might explain the large and still unexplained difference in lithosphere elastic thickness estimated below the two polar caps, which is about 300 km in the North and only 140 km in the South. Assuming a crust in the Northern hemisphere with a thickness of 40 km, a density of 3000 kg/m3 and an enrichment factor in radioactive elements of 5 relative to the primitive mantle, Monte Carlo inversions show that the Southern crust requires a thickness of >60 km, a density between 2700 and 3000 kg/m3 and an enrichment factor of 13-20 to explain such a difference in lithosphere elastic thickness.

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.

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

NASA Astrophysics Data System (ADS)

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

2015-07-01

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

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).

Thermal compatibility of dental ceramic systems using cylindrical and spherical geometries.

PubMed

DeHoff, Paul H; Barrett, Allyson A; Lee, Robert B; Anusavice, Kenneth J

2008-06-01

To test the hypothesis that bilayer ceramic cylinders and spheres can provide valid confirmation of thermal incompatibility stresses predicted by finite element analyses. A commercial core ceramic and an experimental core ceramic were used to fabricate open-ended cylinders and core ceramic spheres. The core cylinders and spheres were veneered with one of four commercial dental ceramics representing four thermally compatible groups and four thermally incompatible groups. Axisymmetric thermal and viscoelastic elements in the ANSYS finite element program were used to calculate temperatures and stresses for each geometry and ceramic combination. This process required a transient heat transfer analysis for each combination to determine input temperatures for the structural model. After fabrication, each specimen was examined visually using fiberoptic transillumination for evidence of cracking. There were 100% failures of the thermally incompatible cylinders while none of the thermally compatible combinations failed. Among the spheres, 100% of the thermally incompatible systems failed, 16% of one of the thermally compatible systems failed, and none of the remaining compatible combinations failed. The calculated stress values were in general agreement with the experimental observations, i.e., low residual stresses for the specimens that did not fail and high residual stresses for the specimens that did fail. Simple screening geometries can be used to identify highly incompatible ceramic combinations, but they do not identify marginally incompatible systems.

Thermal compatibility of dental ceramic systems using cylindrical and spherical geometries

PubMed Central

DeHoff, Paul H.; Barrett, Allyson A.; Lee, Robert B.; Anusavice, Kenneth J.

2009-01-01

Objective To test the hypothesis that bilayer ceramic cylinders and spheres can provide valid confirmation of thermal incompatibility stresses predicted by finite element analyses. Methods A commercial core ceramic and an experimental core ceramic were used to fabricate open-ended cylinders and core ceramic spheres. The core cylinders and spheres were veneered with one of four commercial dental ceramics representing four thermally compatible groups and four thermally incompatible groups. Axisymmetric thermal and viscoelastic elements in the ANSYS finite element program were used to calculate temperatures and stresses for each geometry and ceramic combination. This process required a transient heat transfer analysis for each combination to determine input temperatures for the structural model. Results After fabrication, each specimen was examined visually using fiberoptic transillumination for evidence of cracking. There were 100% failures of the thermally incompatible cylinders while none of the thermally compatible combinations failed. Among the spheres, 100% of the thermally incompatible systems failed, 16% of one of the thermally compatible systems failed, and none of the remaining compatible combinations failed. The calculated stress values were in general agreement with the experimental observations, i.e., low residual stresses for the specimens that did not fail and high residual stresses for the specimens that did fail. Significance Simple screening geometries can be used to identify highly incompatible ceramic combinations, but they do not identify marginally incompatible systems. PMID:17949805

Chemical evidence for differentiation, evaporation and recondensation from silicate clasts in Gujba

NASA Astrophysics Data System (ADS)

Oulton, Jonathan; Humayun, Munir; Fedkin, Alexei; Grossman, Lawrence

2016-03-01

The silicate and metal clasts in CB chondrites have been inferred to form as condensates from an impact-generated vapor plume between a metal-rich body and a silicate body. A detailed study of the condensation of impact-generated vapor plumes showed that the range of CB silicate clast compositions could not be successfully explained without invoking a chemically differentiated target. Here, we report the most comprehensive elemental study yet performed on CB silicates with 32 silicate clasts from nine slices of Gujba analyzed by laser ablation inductively coupled plasma mass spectrometry for 53 elements. Like in other studies of CBs, the silicate clasts are either barred olivine (BO) or cryptocrystalline (CC) in texture. In major elements, the Gujba silicate clasts ranged from chondritic to refractory enriched. Refractory element abundances ranged from 2 to 10 × CI, with notable anomalies in Ba, Ce, Eu, and U abundances. The two most refractory-enriched BO clasts exhibited negative Ce anomalies and were depleted in U relative to Th, characteristic of volatilization residues, while other BO clasts and the CC clasts exhibited positive Ce anomalies with excess U (1-3 × CI), and Ba (1-6 × CI) anomalies indicating re-condensation of ultra-refractory element depleted vapor. The Rare Earth Elements (REE) also exhibit light REE (LREE) enrichment or depletion in several clasts with a range of (La/Sm)CI of 0.9-1.8. This variation in the LREE is essentially impossible to accomplish by processes involving vapor-liquid or vapor-solid exchange of REE, and appears to have been inherited from a differentiated target. The most distinctive evidence for inherited chemical differentiation is observed in highly refractory element (Sc, Zr, Nb, Hf, Ta, Th) systematics. The Gujba clasts exhibit fractionations in Nb/Ta that correlate positively with Zr/Hf and span the range known from lunar and Martian basalts, and exceed the range in Zr/Hf variation known from eucrites. Variations of highly incompatible refractory elements (e.g., Th) against less incompatible elements (e.g., Zr, Sr, Sc) are not chondritic, but exhibit distinctly higher Th abundances requiring a differentiated crust to be admixed with depleted mantle in ratios that are biased to higher crust/mantle ratios than in a chondritic body. The possibility that these variations are due to admixture of refractory inclusion-debris into normal chondritic matter is raised but cannot be definitively tested because existing ;bulk; analyses of CAIs carry artifacts of unrepresentative sampling. The inferences drawn from the compositions of Gujba silicate clasts, here, complement what has been inferred from the compositions of metallic clasts, but provide surprisingly detailed insight into the structure of the target. Evidence that metal and silicate in CB chondrites both formed from impact-generated vapor plumes, taken together with recent work on metallic nodules in E chondrites, and on ordinary chondrites, indicates that chondrule formation occurs by this mechanism quite widely. However, the nature of the impact on the CB body is quite different than the popular conceptions of impact of partially or wholly molten chondritic bodies and the younger (5 Ma) age of CB chondrules is consistent with origin in a disk with more evolved targets and impactors gravitationally perturbed by nascent planets.

Status of volcanic hazard studies for the Nevada Nuclear Waste Storage Investigations. Volume II

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

Crowe, B.M.; Wohletz, K.H.; Vaniman, D.T.

1986-01-01

Volcanic hazard investigations during FY 1984 focused on five topics: the emplacement mechanism of shallow basalt intrusions, geochemical trends through time for volcanic fields of the Death Valley-Pancake Range volcanic zone, the possibility of bimodal basalt-rhyolite volcanism, the age and process of enrichment for incompatible elements in young basalts of the Nevada Test Site (NTS) region, and the possibility of hydrovolcanic activity. The stress regime of Yucca Mountain may favor formation of shallow basalt intrusions. However, combined field and drill-hole studies suggest shallow basalt intrusions are rare in the geologic record of the southern Great Basin. The geochemical patterns ofmore » basaltic volcanism through time in the NTS region provide no evidence for evolution toward a large-volume volcanic field or increases in future rates of volcanism. Existing data are consistent with a declining volcanic system comparable to the late stages of the southern Death Valley volcanic field. The hazards of bimodal volcanism in this area are judged to be low. The source of a 6-Myr pumice discovered in alluvial deposits of Crater Flat has not been found. Geochemical studies show that the enrichment of trace elements in the younger rift basalts must be related to an enrichment of their mantle source rocks. This geochemical enrichment event, which may have been metasomatic alteration, predates the basalts of the silicic episode and is, therefore, not a young event. Studies of crater dimensions of hydrovolcanic landforms indicate that the worst case scenario (exhumation of a repository at Yucca Mountain by hydrovolcanic explosions) is unlikely. Theoretical models of melt-water vapor explosions, particularly the thermal detonation model, suggest hydrovolcanic explosion are possible at Yucca Mountain. 80 refs., 21 figs., 5 tabs.« less

The 1998-2001 submarine lava balloon eruption at the Serreta ridge (Azores archipelago): Constraints from volcanic facies architecture, isotope geochemistry and magnetic data

NASA Astrophysics Data System (ADS)

Madureira, Pedro; Rosa, Carlos; Marques, Ana Filipa; Silva, Pedro; Moreira, Manuel; Hamelin, Cédric; Relvas, Jorge; Lourenço, Nuno; Conceição, Patrícia; Pinto de Abreu, Manuel; Barriga, Fernando J. A. S.

2017-01-01

The most recent submarine eruption observed offshore the Azores archipelago occurred between 1998 and 2001 along the submarine Serreta ridge (SSR), 4-5 nautical miles WNW of Terceira Island. This submarine eruption delivered abundant basaltic lava balloons floating at the sea surface and significantly changed the bathymetry around the eruption area. Our work combines bathymetry, volcanic facies cartography, petrography, rock magnetism and geochemistry in order to (1) track the possible vent source at seabed, (2) better constrain the Azores magma source(s) sampled through the Serreta submarine volcanic event, and (3) interpret the data within the small-scale mantle source heterogeneity framework that has been demonstrated for the Azores archipelago. Lava balloons sampled at sea surface display a radiogenic signature, which is also correlated with relatively primitive (low) 4He/3He isotopic ratios. Conversely, SSR lavas are characterized by significantly lower radiogenic 87Sr/86Sr, 206Pb/204Pb and 208Pb/204Pb ratios than the lava balloons and the onshore lavas from the Terceira Island. SSR lavas are primitive, but incompatible trace-enriched. Apparent decoupling between the enriched incompatible trace element abundances and depleted radiogenic isotope ratios is best explained by binary mixing of a depleted MORB source and a HIMU­type component into magma batches that evolved by similar shallower processes in their travel to the surface. The collected data suggest that the freshest samples collected in the SSR may correspond to volcanic products of an unnoticed and more recent eruption than the 1998-2001 episode.

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.

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.

Geochemistry of the Shuksan greenschists and blueschists, North Cascades, Washington: Variably fractionated and altered metabasalts of oceanic affinity

NASA Astrophysics Data System (ADS)

Dungan, M. A.; Vance, J. A.; Blanchard, D. P.

1983-06-01

The Shuksan schist comprises a structurally coherent, metabasaltic member of the Easton Formation, the uppermost allochthon (Shuksan thrust plate) in the thrust system of the western North Cascades of Washington State. Late Jurassic metamorphism at moderately high P/T produced interlayering of actinolite-bearing greenschist assemblages with blue amphibole-bearing rocks. Major and trace element analyses of twelve greenschist and blueschist samples have been used to establish similarities between the basaltic protolith and moderately to strongly fractionated Type I MORB, to distinguish the effects of seafloor alteration superimposed on the primary igneous chemistry, and to evaluate the origin and nature of the chemical controls which produced the two mineral assemblages. The twelve analyzed samples exhibit moderate to strong LREE depletion, and characteristically low concentrations of other non-labile trace elements such as Nb, Th and Hf. The highly to moderately incompatible elements Ti, P, Nb, Zr, Hf, Y, Sc, and the REE vary by factors of 1.5 to 3.5 within the suite in a systematic pattern, increasing smoothly with increasing total iron. The relative enrichments of these elements are inversely proportional to bulk partition coefficients estimated for fractionation of basaltic magmas. The magnitude of the negative europium anomaly increases with overall incompatible element enrichment. These variations are consistent with the production of a wide spectrum of compositions by different degrees of low pressure fractionation of similar Type I MORB parent magmas. The concentrations of Sr, Rb, Na, and K vary irregularly and do not correlate with the non-labile trace elements. K and Rb are substantially elevated over typical MORB values in most samples and exhibit a consistently lower ratio (K/Rb=400 vs 1000) than fresh MORB. Concentrations of these four elements are believed to have been modified by low temperature seafloor alteration (pre-metamorphic) characterized by the formation of K-rich celadonitic clays, palagonite and minor potassium feldspar. The critical chemical variables that control the occurrence of actinolite and blue amphibole in the Shuksan schists are total iron, Fe2O3-content and Na/Ca (all high in blueschists). The chemical features were largely established by magmatic processes and inherited from the igneous parent rocks; the chemically more evolved samples are blueschists. The Fe2O3-content and Na/Ca, however, may be modified during alteration, rendering initial bulk compositions near the chemical boundary susceptible to changes which may shift rock compositions from one compatibility field to the other. Heterogeneous alteration of pillow lavas and other fragmental deposits, followed by intense flattening during metamorphism, provides a mechanism for generating blueschists and greenschists interlayered on the cm scale.

Observations of 231Pa/ 235U disequilibrium in volcanic rocks

NASA Astrophysics Data System (ADS)

Pickett, David A.; Murrell, Michael T.

1997-04-01

We present here the first survey of ( 231Pa/ 235U) ratios in volcanic rocks; such measurements are made possible by new mass spectrometric techniques. The data place new constraints on the timing and extent of magma source and evolutionary processes, particularly due to the sensitivity of the 231Pa- 235U pair and its intermediate time scale ( 231Pat 1/2 = 33 ky). ( 231Pa/ 235U) is found to vary widely, from 0.2 in carbonatites to 1.1-2.9 in basalts and 0.9-2.2 in arcs. Substantial Pa enrichment is nearly ubiquitous, suggestive of the relative incompatibility of Pa, qualitatively consistent with available partitioning data. The level of 231Pa- 235U disequilibrium typically far exceeds that of 230Th- 238U and is comparable to 226Ra- 230Th. The high ( 231Pa/ 235U) ratios in MORB and other basalts reflect a large degree of discrimination between two incompatible elements, posing challenges for modelling of melt generation and migration. Fundamental differences in ( 231Pa/ 235U) among different basaltic environments are likely related to contrasts in melting zone conditions (e.g., melting rate). Strong ( 231Pa/ 235U) disequilibria in continental basalts, for which ( 230Th/ 238U) disequilibria are small or absent, demonstrate that Pa-U fractionation is possible in both garnet and spinel mantle stability fields. In arcs, correlation of ( 231Pa/ 235U) and ( 230Th/ 238U) is consistent with U enrichment via slab-derived fluids, a process which is additional to the still dominant Pa enrichment. An important new constraint is provided by the observation that the near-equilibrium ( 230Th/ 238U) common to arcs and continental basalts is not typically accompanied by near-equilibrium ( 231Pa/ 235U), arguing against the influence of long magma history, crustal material, or equilibrium mantle sources in affecting decay-series ratios. Small sample sets from two silicic centers illustrate: (1) recent, rapid U enrichment in the magma chamber (El Chichón); and (2) the failure of substantial magma H 2O-CO 2 degassing to effect U-Th-Pa fractionation (Mono Craters).

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.

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.

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.

Geochemical, oxygen, and neodymium isotope compositions of metasediments from the Abitibi greenstone belt and Pontiac Subprovince, Canada: Evidence for ancient crust and Archean terrane juxtaposition

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

Feng, R.; Kerrich, R.; Maas, R.

1993-02-01

The Abitibi greenstone belt (AGB) and Pontiac Subprovince (PS) in the southwestern Superior Province are adjacent greenstone-plutonic and metasedimentary-dominated terranes, respectively, separated by a major fault zone. Metasediments from these two contrasting terranes are compared in terms of major- and trace-element and O- and Nd-isotope compositions, and detrital zircon ages. The following two compositional populations of metasediments are present in the low-grade, Abitibi southern volcanic zone: (1) a mafic-element-enriched population (MEP) characterized by flat, depleted REE patterns; enhanced Mg, Cr, Co, Ni, and Sc; low-incompatible-element contents; and minor or absent normalized negative troughs at Nb, Ta, and Ti; and (2)more » a low-mafic-element population (LMEP) featuring LREE-enriched patterns; enhanced Rb, Cs, Ba, Th, and U contents; and pronounced normalized negative troughs at Nb, Ta, and Ti. These geochemical features are interpreted to indicate that the MEP sediments were derived from an ultramafic- and mafic-dominated oceanic provenance, whereas the LMEP sediments represent mixtures of mafic and felsic are source rocks. The PS metasediments are essentially indistinguishable from Abitibi LMEP on the basis of major-element and transition metal abundances, suggesting comparable types of source rocks and degrees of maturity, but are distinct in terms of some trace elements and O-isotope compositions. The Pontiac metasediments are depleted in [sup 18]O and enriched in Cs, Ba, Pb, Th, U, Nb, Ta, Hf, Zr, and total REE and also have higher ratios of Rb/K, Cs/Rb, Ba/Rb, Ta/Nb, Th/La, and Ba/La relative to the Abitibi LMEP. Two subtypes of REE patterns have been identified in PS metasediments. The first subtype is interpreted to be derived from provenances of mixed mafic and felsic volcanic rocks, whereas the Eu-depleted type has features that are typical of post-Archean sediments or Archean K-rich granites and volcanic equivalents. 100 refs., 9 figs., 4 tabs.« less

Hydrogen Isotopic Composition of Apatite in Northwest Africa 7034: A Record of the "Intermediate" H-Isotopic Reservoir in the Martian Crust?

NASA Technical Reports Server (NTRS)

McCubbin, F. M.; Barnes, J. J.; Santos, A. R.; Boyce, J. W.; Anand, M.; Franchi, I. A.; Agee, C. B.

2016-01-01

Northwest Africa (NWA) 7034 and its pairings comprise a regolith breccia with a basaltic bulk composition [1] that yields a better match than any other martian meteorite to visible-infrared reflectance spectra of the martian surface measured from orbit [2]. The composition of the fine-grained matrix within NWA 7034 bears a striking resemblance to the major element composition estimated for the martian crust, with several exceptions. The NWA 7034 matrix is depleted in Fe, Ti, and Cr and enriched in Al, Na, and P [3]. The differences in Al and Fe are the most substantial, but the Fe content of NWA 7034 matrix falls within the range reported for the southern highlands crust [6]. It was previously suggested by [4] that NWA 7034 was sourced from the southern highlands based on the ancient 4.4 Ga ages recorded in NWA 7034/7533 zircons [4, 5]. In addition, the NWA 7034 matrix material is enriched in incompatible trace elements by a factor of 1.2-1.5 [7] relative to estimates of the bulk martian crust. The La/Yb ratio of the bulk martian crust is estimated to be approximately 3 [7], and the La/Yb of the NWA 7034 matrix materials ranges from approximately 3.9 to 4.4 [3, 8], indicating a higher degree of LREE enrichment in the NWA 7034 matrix materials. This elevated La/Yb ratio and enrichment in incompatible lithophile trace elements is consistent with NWA 7034 representing a more geochemically enriched crustal terrain than is represented by the bulk martian crust, which would be expected if NWA 7034 represents the bulk crust from the southern highlands. Given the similarities between NWA 7034 and the martian crust, NWA 7034 may represent an important sample for constraining the composition of the martian crust, particularly the ancient highlands. In the present study, we seek to constrain the H isotopic composition of the martian crust using Cl-rich apatite in NWA 7034. Usui et al., [9] recently proposed that a H isotopic reservoir exists within the martian crust that has a H-isotopic composition that is intermediate (dD of 1000-2000per mille) between an isotopically light mantle (Delta D is less than 275per mille [10]) and an isotopically heavy atmosphere (dD of 2500-6100per mille [11, 12]). Apatites in NWA 7034 occur in a number of lithologic domains, however apatites across all lithologic domains have been affected by a Pb-loss event at about 1.5 Ga before present [5], so they are unlikely to have retained a primary composition and are more likely to have equilibrated with fluids within the martian crust that may or may not have exchanged with the martian atmosphere. Equilibration of apatite with crustal fluids is further supported by the chlorine-rich compositions exhibited by apatites in NWA 7034 in comparison to apatites from other martian meteorites (Figure 1; [13]). Cl is more hydrophilic than F, which promotes formation of Cl-rich apatite compositions in fluid-rich systems [e.g., 14, 15-17].

Basin Excavation, Lower Crust, Composition, and Bulk Moon Mass balance in Light of a Thin Crust

NASA Technical Reports Server (NTRS)

Jolliff, B. L.; Korotev, R. L.; Ziegler, R. A.

2013-01-01

New lunar gravity results from GRAIL have been interpreted to reflect an overall thin and low-density lunar crust. Accordingly, crustal thickness has been modeled as ranging from 0 to 60 km, with thinnest crust at the locations of Crisium and Moscoviense basins and thickest crust in the central farside highlands. The thin crust has cosmochemical significance, namely in terms of implications for the Moon s bulk composition, especially refractory lithophile elements that are strongly concentrated in the crust. Wieczorek et al. concluded that the bulk Moon need not be enriched compared to Earth in refractory lithophile elements such as Al. Less Al in the crust means less Al has been extracted from the mantle, permitting relatively low bulk lunar mantle Al contents and low pre- and post-crust-extraction values for the mantle (or the upper mantle if only the upper mantle underwent LMO melting). Simple mass-balance calculations using the method of [4] suggests that the same conclusion might hold for Th and the entire suite of refractory lithophile elements that are incompatible in olivine and pyroxene, including the KREEP elements, that are likewise concentrated in the crust.

Compositional heterogeneity of the Sugarloaf melilite nephelinite flow, Honolulu Volcanics, Hawai'i

NASA Astrophysics Data System (ADS)

Clague, David A.; Frey, Frederick A.; Garcia, Michael O.; Huang, Shichun; McWilliams, Michael; Beeson, Melvin H.

2016-07-01

The Sugarloaf flow is a melilite nephelinite erupted from the Tantalus rift during rejuvenated-stage volcanism on O'ahu, the Honolulu Volcanics. The flow ponded in Mānoa Valley forming a ∼15 m thick flow which was cored and sampled in a quarry. Nepheline from a pegmatoid segregation in the flow yielded a 40Ar-39Ar age of 76 ka. This age, combined with others, indicates that the Tantalus rift eruptions are some of the youngest on O'ahu. Honolulu Volcanics erupt on average about every 35-40 ka indicating that future eruptions are possible. We evaluated the compositional variability of 19 samples from the flow, including 14 from the core. Twelve samples are representative of the bulk flow, four are dark- or light-colored variants, one is a heavy rare earth element (REE)-enriched pegmatoid, and two visually resemble the bulk flow, but have chemical characteristics of the dark and light variants. Our objective was to determine intraflow heterogeneity in mineralogy and composition. Variable abundances of Na2O, K2O, Sr, Ba, Rb, Pb and U in the flow were caused by post-eruptive mobility in a vapor phase, most likely during or soon after flow emplacement, and heterogeneous deposition of secondary calcite and zeolites. Relative to fine-grained samples, a pegmatoid vein that crosscuts the flow is enriched in incompatible trace elements except Sr and TiO2. Element mobility after eruption introduced scatter in trace element ratios including light-REE/heavy-REE, and all ratios involving mobile elements K, Rb, Ba, Sr, Pb, and U. Lavas from some of the 37 Honolulu Volcanics vents have crosscutting REE patterns in a primitive mantle-normalized plot. Such patterns have been interpreted to reflect variable amounts of residual garnet during partial melting. Previous studies of lavas from different vents concluded that garnet, phlogopite, amphibole, and Fe-Ti oxides were residual phases of the partial melting processes that created the Honolulu Volcanics (Clague and Frey, 1982; Yang et al., 2003). However post-eruptive processes in the Sugarloaf flow also produced crossing REE patterns. Eruptions on the Tantalus rift, including the Sugarloaf flow, produced volatile- and crystal-rich ash with interstitial glass and melt inclusions in olivine containing 4.2-6.4 wt% MgO compared to the flow average of 11.8 wt%. This flow erupted as a partially crystallized viscous magma at least 100 °C below its liquidus. The slow advance and cooling of the 15-m thick 'a' ā low promoted the segregation of pegmatoids, formation of light and dark bands with differing proportions of melilite and clinopyroxene, and induced volatile-enhanced mobility of incompatible elements.

Protecting and Preserving Rail Corridors Against Encroachment of Incompatible Uses.

DOT National Transportation Integrated Search

2008-01-01

Rail Corridor preservation and planning for the purpose of reducing or restricting incompatible development is an : area of growing importance. This report provides an overview regarding encroachment and the elements that : contribute to potentially ...

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.

Petrogenesis and tectonic significance of the calc-alkaline, bimodal Aztec Wash pluton, Eldorado Mountains, Colorado River extensional corridor

NASA Astrophysics Data System (ADS)

Falkner, Claudia M.; Miller, Calvin F.; Wooden, Joseph L.; Heizler, Matthew T.

1995-06-01

The 15.7 Ma Aztec Wash pluton is located in the central Eldorado Mountains of the Colorado River extensional corridor in southern Nevada, immediately south of the well-known imbricated volcanic sequence that has been widely cited in studies of extensional tectonism (e.g., Anderson, 1971). It is a shallow level (≤5 km), essentially bimodal complex, primarily made up of granite (˜72 wt % SiO2) and diabase and diorite (˜54 wt % SiO2), with minor amounts of more mafic, intermediate, and highly evolved rocks. The mafic and felsic magmas mingled extensively but mixed only to a limited extent. Late synplutonic mafic and felsic dikes represent continuing injection of the same bimodal magmas. The mafic rocks have high incompatible element concentrations (e.g., K2O ˜ 3 wt %, Ba ˜ 1600 ppm, light rare earth elements 350 × chondrite) and enriched isotopic compositions (ɛNd -7.5, 87Sr/86Sr 0.708); generation in ancient, enriched mantle lithosphere with limited subsequent crustal contamination is inferred. The granite is more potassic (˜5 wt %) than the mafic rocks, but it has comparable or lower concentrations of most incompatible elements; its isotopic composition (ɛNd -10, 87Sr/86Sr 0.710) is intermediate between those of the mafic rocks and local ancient crust. The granites thus indicate hybridization of the crust by mafic magma, but it is unclear whether this hybridization occurred at deeper levels in this magmatic system, or during an earlier mid-Tertiary or Mesozoic magmatic event. Emplacement of the Aztec Wash pluton preceded peak east west extension in the northern Eldorado Mountains (˜15.2 Ma (Gans et al., 1994)), but it coincided with at least modest extension as indicated by the uniform NS orientation of the late dikes and the mafic injections into the magma chamber. Total extension and tilting of the pluton after crystallization was minor, in contrast to the east tilted area to the north and west tilted area to the south. Timing and style of extension are thus consistent with the pluton's location within, and perhaps mechanical influence on, a major accommodation zone, as suggested by Faulds et al. (1990) and Faulds (1994).

The behavior of chalcophile elements during magmatic differentiation as observed in Kilauea Iki lava lake, Hawaii

NASA Astrophysics Data System (ADS)

Greaney, Allison T.; Rudnick, Roberta L.; Helz, Rosalind T.; Gaschnig, Richard M.; Piccoli, Philip M.; Ash, Richard D.

2017-08-01

We quantify the behavior of Cu, Ga, Ge, As, Mo, Ag, Cd, In, Sn, Sb, W, Tl, Pb, and Bi during the differentiation of a picritic magma in the Kilauea Iki lava lake, Hawaii, using whole rock and glass differentiation trends, as well as partition coefficients in Cu-rich sulfide blebs and minerals. Such data allow us to constrain the partitioning behavior of these elements between sulfide and silicate melts, as well as the chalcophile element characteristics of the mantle source of the Kilauea lavas. Nearly all of the elements are generally incompatible on a whole-rock scale, with concentrations increasing exponentially below ∼6 wt% MgO. However, in-situ laser ablation data reveal that Cu, Ag, Bi, Cd, In, Pb, and Sn are chalcophile; As, Ge, Sb, and Tl are weakly chalcophile to lithophile; and Mo, Ga, and W are lithophile. The average Dsulfide/silicate melt values are: DAg = 1252 ± 1201 (2SD), DBi = 663 ± 576, DCd = 380 ± 566, DIn = 40 ± 34, DPb = 34 ± 18, DSn = 5.3 ± 3.6, DAs = 2.4 ± 7.6, DGe = 1.6 ± 1.4, DSb = 1.3 ± 1.5, DTl = 1.1 ± 1.7, DMo = 0.56 ± 0.6, DGa = 0.10 ± 0.3, and DW = 0.11 ± 0.1. These findings are consistent with experimental partitioning studies and observations of Ni-rich sulfide liquid in mid-ocean ridge basalts (MORB), despite the different compositions of the KI sulfides. The KI glasses and whole rocks are enriched in As, Ag, Sb, W, and Bi, relative to elements of similar compatibility (as established by abundances in MORB), mimicking enrichments found in basalts from the Manus back arc basin (Jenner et al., 2012) and the upper continental crust (UCC). These enrichments suggest the presence of terrigenous sediments in the Kilauea mantle source. The KI source is calculated to be a mixture of depleted MORB mantle (DMM) and 10-20% recycled crust composed of MORB and minor terrigenous sediments.

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.

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.

Zircon/fluid trace element partition coefficients measured by recrystallization of Mud Tank zircon at 1.5 GPa and 800-1000 °C

NASA Astrophysics Data System (ADS)

Ayers, John C.; Peters, Timothy J.

2018-02-01

Hydrothermal zircon grains have trace element characteristics such as low Th/U, high U, and high rare earth element (REE) concentrations that distinguish them from magmatic, metamorphic, and altered zircon grains, but it is unclear whether these characteristics result from distinctive fluid compositions or zircon/fluid fractionation effects. New experiments aimed at measuring zircon/fluid trace element partition coefficients Dz/f involved recrystallizing natural Mud Tank zircon with low trace element concentrations in the presence of H2O, 1 m NaOH, or 1 m HCl doped with ∼1000 ppm of rare earth elements (REE), Y, U and Th and ∼500 ppm of Li, B, P, Nb, Ba, Hf, and Ta. Experiments were run for 168 h at 1.5 GPa, 800-1000 °C, and fO2 = NNO in a piston cylinder apparatus using the double capsule method. LA-ICP-MS analysis shows that run product zircon crystals have much higher trace element concentrations than in Mud Tank zircon starting material. Dz/f values were estimated from run product zircon analyses and bulk composition using mass balance. Most elements behave incompatibly, with median Dz/f being highest for Hf = 8 and lowest for B = 0.02. Addition of NaOH or HCl had little influence on Dz/f values. Dz/f for LREE are anomalously high, likely due to contamination of run product zircon with quenched solutes enriched in incompatible elements, so DLREE were estimated using lattice strain theory. Brice curves for +3 ions yield zircon/fluid DLu/DLa of ∼800-5000. A Brice curve fit to +4 ions yielded DCe4+ values. Estimated concentrations of Ce3+ and Ce4+ show that the average Ce4+/Ce3+ in zircon of 27 is much higher than in fluid of 0.02. Th and U show little fractionation, with median DTh/DU = 0.7, indicating that the low Th/U in natural hydrothermal zircon is inherited from the fluid. Natural fluid compositions estimated from measured Dz/f and published compositions of hydrothermal zircon grains from aplite and eclogite reflect the mineralogy of the host rock, e.g., fluid in equilibrium with eclogite garnet is depleted in heavy REE relative to middle REE, and has low Th/U.

Experimental and natural partitioning behaviour of trace-elements between hydrous evolved melts, amphibole, plagioclase, and clinopyroxene at shallow crustal conditions

NASA Astrophysics Data System (ADS)

Iveson, A. A.; Webster, J. D.; Rowe, M. C.; Neill, O. K.

2016-12-01

New experimental data for crystal-melt partitioning behaviour of a suite of trace-elements are presented. Hydrous rhyo-dacitic starting glasses from Mt. Usu, Japan, were doped with Li, Sc, Cr, Mn, Ni, Cu, Zn, Ga, Rb, Sr, Y, Nb, Mo, Ba, W, and Pb. Aqueous solutions were added such that the volatile phase(s) coexisting with amphibole, plagioclase, and clinopyroxene at run conditions buffered the S, F, and Cl contents of the melts. Internally-heated pressure vessel experiments were conducted at 750-850 °C, 1.0-4.0 Kbar, and ƒO2 ≈ NNO-NNO+2 log units. Major- and minor-element concentrations in the phenocrysts and glasses were analysed by EPMA, and trace-element contents by SIMS and/or LA-ICP-MS. The long run durations, homogeneous glasses, and minimal compositional zonation of crystals suggest that near-equilibrium conditions were achieved. Results of multiple phenocryst and glass analyses show that Nernst-type crystal-melt partition coefficients for these elements range from strongly incompatible e.g. Dmineral/melt ≈ 0 for Nb into plagioclase, to moderately incompatible e.g. Dmineral/melt ≈ 0.75 for Ga into amphibole, to strongly compatible e.g. Dmineral/melt > 50 for Ni into amphibole and clinopyroxene. Furthermore, unlike other elements investigated, partitioning of Li between phenocrysts and melt is similar for all three phases, with average DLicpx/melt ≈ 0.26 > DLiplag/melt ≈ 0.24 > DLiamph/melt ≈ 0.19. Relative to major-element composition of crystalline phases, the temperature, pressure, and ƒO2 conditions do not appear to strongly affect this behaviour. The incorporation of F and Cl into amphiboles is also consistent with the Fe-F and Mg-Cl crystallographic avoidance principles. Importantly, across two orders of magnitude in concentration, partitioning behaviours of all analysed trace-elements appear to obey Henry's Law. The experimental data are integrated with new amphibole, plagioclase, and pyroxene analyses from eruptive products of Augustine and Mt. St. Helens volcanoes. The results are applicable to understanding processes governing melt evolution during shallow magma storage and formation of economic metal deposits, where the crystallisation of porphyry-type magmas leads to fluid exsolution, and enrichment and transport of such trace- and ore-elements.

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.

Geochemistry of komatiites and basalts from the Rio das Velhas and Pitangui greenstone belts, São Francisco Craton, Brazil: Implications for the origin, evolution, and tectonic setting

NASA Astrophysics Data System (ADS)

Verma, Sanjeet K.; Oliveira, Elson P.; Silva, Paola M.; Moreno, Juan A.; Amaral, Wagner S.

2017-07-01

The Neoarchean Rio das Velhas and Pitangui greenstone belts are situated in the southern São Francisco Craton, Minas Gerais, Brazil. These greenstone belts were formed between ca. 2.79-2.73 Ga, and consist mostly of mafic to ultramafic volcanics and clastic sediments, with minor chemical sediments and felsic volcanics that were metamorphosed under greenschist facies. Komatiites are found only in the Rio das Velhas greenstone belt, which is composed of high-MgO volcanic rocks that have been identified as komatiites and high-Mg basalts, based on their distinctive geochemical characteristics. The Rio das Velhas komatiites are composed of tremolite + actinolite + serpentine + albite with a relict spinifex-texture. The Rio das Velhas komatiites have a high magnesium content ((MgO)adj ≥ 28 wt.%), an Al-undepleted Munro-type [(Al2O3/TiO2)adj and (CaO/Al2O3)adj] ratio ranging from 27 to 47 and 0.48 to 0.89, relatively low abundances of incompatible elements, a depletion of light rare earth elements (LREE), a pattern of non-fractionated heavy rare- earth elements (HREE), and a low (Gd/Yb)PM ratio (≤ 1.0). Negative Ce anomalies suggest that alteration occurred during greenschist facies metamorphism for the komatiites and high-Mg basalts. The low [(Gd/Yb)PM < 1.0] and [(CaO/Al2O3)adj < 0.9)], high [(Al2O3/TiO2)adj > 18] and high HREE, Y, and Zr content suggest that the Rio das Velhas komatiites were derived from the shallow upper mantle without garnet involvement in the residue. The chemical compositions [(Al2O3/TiO2)adj, (FeO)adj, (MgO)adj, (CaO/Al2O3)adj, Na, Th, Ta, Ni, Cr, Zr, Y, Hf, and REE] indicate that the formation of the komatiites, high-Mg basalts and basalts occurred at different depths and temperatures in a heterogeneous mantle. The komatiites and high-Mg basalts melted at liquidus temperatures of 1450-1550 °C. The Pitangui basalts are enriched in the highly incompatible LILE (large-ion lithophile elements) relative to the moderately incompatible HFS (high field strength) elements. The Zr/Th ratio ranging from 76 to 213 and the relationship between the Nb/Th and Th/Yb ratios indicate that there is no crustal contamination in the Pitangui greenstone basalts. New multi-dimensional discrimination diagrams and conventional normalized multi-element diagrams indicate an island arc (IA) setting for the komatiites and high-Mg basalts from the Rio das Velhas and a mid ocean-ridge (MOR) to IA setting for the basalts from the Pitangui greenstone belts.

Volatile element content of the heterogeneous upper mantle

NASA Astrophysics Data System (ADS)

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

2014-12-01

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

Eocene slab breakoff of Neotethys as suggested by dioritic dykes in the Gangdese magmatic belt, southern Tibet

NASA Astrophysics Data System (ADS)

Ma, Xuxuan; Xu, Zhiqin; Meert, Joseph G.

2016-04-01

The Gangdese magmatic belt in southern Tibet demarcates an important boundary between the Indian and Eurasian plates. Due to its location and magmatic evolutionary history, it is key to understanding both the history of Neotethys closure and the Indo-Asian collisional process. This study presents new geochronological and geochemical data for dioritic dykes in the southern Gangdese magmatic belt in southern Tibet. U-Pb geochronological results reveal that the dykes were emplaced at ca. 41 Ma and thus broadly coeval with the 40-38 Ma Dazi volcanics and the 42-40 Ma Gaoligong-Tengliang basaltic dykes. Geochemically, these dykes are characterized by alkaline signature, high Mg# (57-63) and low TiO2 contents ( 0.9-1.0), showing notable enrichment of light rare earth elements relative to the heavy rare earth elements, enrichment of incompatible elements (i.e. Cs, Rb, Ba, Th and U), and depletion of high field strength elements (i.e. Nb, Ta and Ti). In addition, a large variation of zircon εHf(t) values (- 10 to + 13) was shown, implying heterogeneity of magma sources. A heterogeneous source is also suggested by the occurrence of xenocrysts in the dykes. These observations suggest that the magma source of the dykes was dominated by partial melting of lithospheric mantle and then subsequently contaminated by crustal material during ascent. In combination with other geological data in the region, we suspect that the slab slicing of the Neotethys played a key role in the formation of the lithospheric mantle-derived dioritic dykes and adakitic granite, asthenosphere-derived volcanics, basaltic dykes, as well as the recently reported strongly fractionated granites.

Evolution and Molecular Control of Hybrid Incompatibility in Plants

PubMed Central

Chen, Chen; E, Zhiguo; Lin, Hong-Xuan

2016-01-01

Postzygotic reproductive isolation (RI) plays an important role in speciation. According to the stage at which it functions and the symptoms it displays, postzygotic RI can be called hybrid inviability, hybrid weakness or necrosis, hybrid sterility, or hybrid breakdown. In this review, we summarized new findings about hybrid incompatibilities in plants, most of which are from studies on Arabidopsis and rice. Recent progress suggests that hybrid incompatibility is a by-product of co-evolution either with “parasitic” selfish elements in the genome or with invasive microbes in the natural environment. We discuss the environmental influences on the expression of hybrid incompatibility and the possible effects of environment-dependent hybrid incompatibility on sympatric speciation. We also discuss the role of domestication on the evolution of hybrid incompatibilities. PMID:27563306

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.

Contrasting petrogenesis of spatially related carbonatites from Samalpatti and Sevattur, Tamil Nadu, India

NASA Astrophysics Data System (ADS)

Ackerman, Lukáš; Magna, Tomáš; Rapprich, Vladislav; Upadhyay, Dewashish; Krátký, Ondřej; Čejková, Bohuslava; Erban, Vojtěch; Kochergina, Yulia V.; Hrstka, Tomáš

2017-07-01

Two Neoproterozoic carbonatite suites of spatially related carbonatites and associated silicate alkaline rocks from Sevattur and Samalpatti, south India, have been investigated in terms of petrography, chemistry and radiogenic-stable isotopic compositions in order to provide further constraints on their genesis. The cumulative evidence indicates that the Sevattur suite is derived from an enriched mantle source without significant post-emplacement modifications through crustal contamination and hydrothermal overprint. The stable (C, O) isotopic compositions confirm mantle origin of Sevattur carbonatites with only a modest difference to Paleoproterozoic Hogenakal carbonatite, emplaced in the same tectonic setting. On the contrary, multiple processes have shaped the petrography, chemistry and isotopic systematics of the Samalpatti suite. These include pre-emplacement interaction with the ambient crustal materials with more pronounced signatures of such a process in silicocarbonatites. Calc-silicate marbles present in the Samalpatti area could represent a possible evolved end member due to the inability of common silicate rocks (pyroxenites, granites, diorites) to comply with radiogenic isotopic constraints. In addition, Samalpatti carbonatites show a range of C-O isotopic compositions, and δ13CV-PDB values between + 1.8 and + 4.1‰ found for a sub-suite of Samalpatti carbonatites belong to the highest values ever reported for magmatic carbonates. These heavy C-O isotopic signatures in Samalpatti carbonatites could be indicative of massive hydrothermal interaction with carbonated fluids. Unusual high-Cr silicocarbonatites, discovered at Samalpatti, seek their origin in the reaction of pyroxenites with enriched mantle-derived alkali-CO2-rich melts, as also evidenced by mantle-like O isotopic compositions. Field and petrographic observations as well as isotopic constraints must, however, be combined with the complex chemistry of incompatible trace elements as indicated from their non-uniform systematics in carbonatites and their individual fractions. We emphasise that, beside common carriers of REE like apatite, other phases may be important for incompatible element budgets, such as mckelveyite-(Nd) and kosmochlor, found in these carbonatites. Future targeted studies, including in-situ techniques, could help further constrain temporal and petrologic conditions of formation of Sevattur and Samalpatti carbonatite bodies.

Identification of misexpressed genetic elements in hybrids between Drosophila-related species.

PubMed

Lopez-Maestre, Hélène; Carnelossi, Elias A G; Lacroix, Vincent; Burlet, Nelly; Mugat, Bruno; Chambeyron, Séverine; Carareto, Claudia M A; Vieira, Cristina

2017-01-16

Crosses between close species can lead to genomic disorders, often considered to be the cause of hybrid incompatibility, one of the initial steps in the speciation process. How these incompatibilities are established and what are their causes remain unclear. To understand the initiation of hybrid incompatibility, we performed reciprocal crosses between two species of Drosophila (D. mojavensis and D. arizonae) that diverged less than 1 Mya. We performed a genome-wide transcriptomic analysis on ovaries from parental lines and on hybrids from reciprocal crosses. Using an innovative procedure of co-assembling transcriptomes, we show that parental lines differ in the expression of their genes and transposable elements. Reciprocal hybrids presented specific gene categories and few transposable element families misexpressed relative to the parental lines. Because TEs are mainly silenced by piwi-interacting RNAs (piRNAs), we hypothesize that in hybrids the deregulation of specific TE families is due to the absence of such small RNAs. Small RNA sequencing confirmed our hypothesis and we therefore propose that TEs can indeed be major players of genome differentiation and be implicated in the first steps of genomic incompatibilities through small RNA regulation.

Identification of misexpressed genetic elements in hybrids between Drosophila-related species

PubMed Central

Lopez-Maestre, Hélène; Carnelossi, Elias A. G.; Lacroix, Vincent; Burlet, Nelly; Mugat, Bruno; Chambeyron, Séverine; Carareto, Claudia M. A.; Vieira, Cristina

2017-01-01

Crosses between close species can lead to genomic disorders, often considered to be the cause of hybrid incompatibility, one of the initial steps in the speciation process. How these incompatibilities are established and what are their causes remain unclear. To understand the initiation of hybrid incompatibility, we performed reciprocal crosses between two species of Drosophila (D. mojavensis and D. arizonae) that diverged less than 1 Mya. We performed a genome-wide transcriptomic analysis on ovaries from parental lines and on hybrids from reciprocal crosses. Using an innovative procedure of co-assembling transcriptomes, we show that parental lines differ in the expression of their genes and transposable elements. Reciprocal hybrids presented specific gene categories and few transposable element families misexpressed relative to the parental lines. Because TEs are mainly silenced by piwi-interacting RNAs (piRNAs), we hypothesize that in hybrids the deregulation of specific TE families is due to the absence of such small RNAs. Small RNA sequencing confirmed our hypothesis and we therefore propose that TEs can indeed be major players of genome differentiation and be implicated in the first steps of genomic incompatibilities through small RNA regulation. PMID:28091568

Evidence for the presence of carbonate melt during the formation of cumulates in the Colli Albani Volcanic District, Italy

NASA Astrophysics Data System (ADS)

Shaw, Cliff S. J.

2018-06-01

Fergusite and syenite xenoliths and mafic lapilli from two locations in the Villa Senni ignimbrite of the Colli Albani Volcanic District show evidence for fractionation of a silicate magma that led to exsolution of an immiscible carbonate melt. The fergusite xenoliths are divided into two groups on the basis of their clinopyroxene compositions. Group 1 clinopyroxene records the crystallisation of a silicate melt and enrichment of the melt in Al, Ti and Mn and depletion in Si as well as enrichment in incompatible trace elements. The second group of clinopyroxene compositions (group 2) comes mainly from Ba-F-phlogopite- and Ti-andradite-bearing fergusites. They have significantly higher Si and lower Al and Ti and, like the coexisting phlogopite and garnet are strongly enriched in Mn. The minerals in the fergusites containing group 2 clinopyroxene are enriched in Ba, Sr, Cs, V and Li all of which are expected to partition strongly into a carbonate melt phase relative to the coexisting silicate melt. The compositional data suggest that the group 1 fergusites record sidewall crystallisation of CO2-rich silicate melt and that once the melt reached a critical degree of fractionation, carbonate melt exsolved. The group 2 fergusites record continued crystallisation in this heterogeneous silicate - carbonate melt system. Composite xenoliths of fergusite and thermometamorphic skarn record contact times of hundreds to a few thousand years indicating that fractionation and assimilation was relatively rapid.

Geochemical and Depth Variations at the Galápagos 93.25˚W Propagating Rift

NASA Astrophysics Data System (ADS)

Rotella, M.; Sinton, J.; Mahoney, J.; Chazey, W.

2006-12-01

The 93.25°W propagating rift on the Galápagos Spreading Center (GSC) differs markedly from the better-known propagator at 95.5°W in having the morphology of a classic overlapping spreading center (~24 km of overlap and 7.5 km of offset). It has a higher propagation rate (70 vs 48 mm/yr) [Wilson & Hey, JGR v. 100, 1995] and is breaking through younger crust (260 vs 910 ka); overall magma supply is ~20% greater, as the area is closer to the Galápagos hotspot. The overlapping limbs lack pronounced bathymetric lows, instead they are up to 150 m shallower than the surrounding axial ridges away from the offset. Lavas are T-MORB; failing rift lavas show a slight increase in Mg within the overlap zone but propagating rift lavas lack the strong fractionation anomaly that characterizes the propagating limb at 95.5°W and many other propagating rifts. New major and trace element data on 28 samples from 24 dredge stations along a 175 km section of the GSC spanning the 93.25°W offset indicate significant, systematic variations in mantle sources and melting processes on each limb of the system. Fractionation-corrected ratios of highly to moderately incompatible elements (e.g. La/Yb, Sm/Yb, Zr/Y) show constant values along the propagating rift east of 93.2°W, but within the overlap zone these ratios increase sharply up to a factor of 1.5, then gradually decline to the west. In contrast, the failing rift shows constant to moderately increasing ratios as the overlap zone is approached from the west, with lower overall ratios within the zone. These variations could be interpreted to reflect a counter-intuitive relationship of gradually increasing extent of partial melting with progressive failure of the dying rift, consistent with the striking shoaling of the failing limb, or melting of incompatible-element depleted mantle. Variations along the eastern, propagating rift suggest either a sharp decrease in extent of melting or tapping of a more incompatible-element-enriched mantle source within the overlap zone. Limited Nd-Pb-Sr isotopic data suggest source variations are required in addition to variations in extent of melting. Thus, in contrast to other well-documented propagators where geochemical variations are dominated by magma chamber effects, variations around the 93.25°W system appear to be dominated by melting and source.

Collisional erosion and the non-chondritic composition of the terrestrial planets.

PubMed

O'Neill, Hugh St C; Palme, Herbert

2008-11-28

The compositional variations among the chondrites inform us about cosmochemical fractionation processes during condensation and aggregation of solid matter from the solar nebula. These fractionations include: (i) variable Mg-Si-RLE ratios (RLE: refractory lithophile element), (ii) depletions in elements more volatile than Mg, (iii) a cosmochemical metal-silicate fractionation, and (iv) variations in oxidation state. Moon- to Mars-sized planetary bodies, formed by rapid accretion of chondrite-like planetesimals in local feeding zones within 106 years, may exhibit some of these chemical variations. However, the next stage of planetary accretion is the growth of the terrestrial planets from approximately 102 embryos sourced across wide heliocentric distances, involving energetic collisions, in which material may be lost from a growing planet as well as gained. While this may result in averaging out of the 'chondritic' fractionations, it introduces two non-chondritic chemical fractionation processes: post-nebular volatilization and preferential collisional erosion. In the latter, geochemically enriched crust formed previously is preferentially lost. That post-nebular volatilization was widespread is demonstrated by the non-chondritic Mn/Na ratio in all the small, differentiated, rocky bodies for which we have basaltic samples, including the Moon and Mars. The bulk silicate Earth (BSE) has chondritic Mn/Na, but shows several other compositional features in its pattern of depletion of volatile elements suggestive of non-chondritic fractionation. The whole-Earth Fe/Mg ratio is 2.1+/-0.1, significantly greater than the solar ratio of 1.9+/-0.1, implying net collisional erosion of approximately 10 per cent silicate relative to metal during the Earth's accretion. If this collisional erosion preferentially removed differentiated crust, the assumption of chondritic ratios among all RLEs in the BSE would not be valid, with the BSE depleted in elements according to their geochemical incompatibility. In the extreme case, the Earth would only have half the chondritic abundances of the highly incompatible, heat-producing elements Th, U and K. Such an Earth model resolves several geochemical paradoxes: the depleted mantle occupies the whole mantle, is completely outgassed in (40)Ar and produces the observed (4)He flux through the ocean basins. But the lower radiogenic heat production exacerbates the discrepancy with heat loss.

MG Isotopic Measurement of FIB-Isolated Presolar Silicate Grains

NASA Technical Reports Server (NTRS)

Messenger, Scott R.; Nguyen, A.; Ito, M.; Rahman, Z.

2010-01-01

The majority of presolar oxide and silicate grains are ascribed to origins in low-mass red giant and asymptotic giant branch (AGB) stars based on their O isotopic ratios. However, a minor population of these grains (< 10%) has O isotopic ratios incompatible with these sources. Two principle alternative sources are higher-than-solar metallicity (Z) stars or, more likely, supernovae (SN) [1-3]. These rare (Group 4) grains [3] are characterized by enrichments in O-18, and typically also enrichments in O-17. An even rarer subset of grains with extremely large enrichments in O-17 and smaller depletions in O-18 were suggested to come from binary star systems [2]. To establish the origins of these isotopically unusual grains, it is necessary to examine isotopic systems in addition to O. Presolar silicates offer several elements diagnostic of their stellar sources and nuclear processes, including O, Si, Mg, Fe and Ca. However, the database for minor element isotopic compositions in silicates is seriously lacking. To date only two silicate grains have been analyzed for Mg [4] or Fe [5]. One major complicating factor is their small size (average 230 nm), which greatly limits the number of measurements that can be performed on any one grain and makes it more difficult to obtain statistically relevant data. This problem is compounded because the grains are identified among isotopically solar silicates, which contribute a diluting signal in isotopic measurements [1]. Thus, relatively small isotopic anomalies are missed due to this dilution effect. By applying focused ion beam (FIB) milling, we obtain undiluted Mg isotopic ratios of isolated rare presolar silicate grains to investigate their sources.

The petrogenesis of Gorgona komatiites, picrites and basalts: new field, petrographic and geochemical constraints

NASA Astrophysics Data System (ADS)

Kerr, A. C.; Marriner, G. F.; Arndt, N. T.; Tarney, J.; Nivia, A.; Saunders, A. D.; Duncan, R. A.

1996-04-01

Gorgona Island, Colombia is remarkable not only because it contains the only Phanerozoic komatiites, but also because it has mafic to ultramafic lavas with a wide range of compositions, from moderately enriched to extremely depleted (relative to Bulk Earth). The komatiite flows are, in many respects similar to Archaean komatiites; they formed from MgO-rich (18%) liquids and have upper spinifex zones and lower cumulate zones. The cumulate zones of Archaean komatiites contain many solid grains, in contrast more than 90% of the olivine in the Gorgona cumulates is highly skeletal. This combined with the fact that the Gorgona cumulate zones are thinner than those in Archaean komatiites, suggests that the komatiite magma became strongly superheated en route to the surface. The komatiites have trace element contents intermediate between those of the basalts and the ultramafic tuffs. Some basalts have isotope compositions indicative of long-term enrichment in incompatible elements, whereas other basalts and ultramafic volcanics have isotopic signatures that imply corresponding depletion. It is apparent that the plume source region of the Gorgona magmas was markedly heterogeneous, with at least two source components contributing to the observed variation in composition. This heterogeneity may have resulted from the incorporation of different components into the plume source, or it may be the result of complex melting and melt extraction processes during the ascent of a heterogeneous plume. Despite earlier suggestions that there may have been a significant age gap between depleted komatiite and basalt flows and the enriched basalts, new 40Ar- 39Ar dating of basalts and gabbros are more consistent with all being generated at 87 Ma during formation of the Caribbean/Colombian plateau, possibly at the Galapagos hotspot.

Variation in trace element content of magnetite crystallized from a fractionating sulfide liquid, Sudbury, Canada: Implications for provenance discrimination

NASA Astrophysics Data System (ADS)

Dare, Sarah A. S.; Barnes, Sarah-Jane; Beaudoin, Georges

2012-07-01

Laser ablation ICP-MS analysis has been applied to many accessory minerals in order to understand better the process by which the rock formed and for provenance discrimination. We have determined trace element concentrations of Fe-oxides in massive sulfides that form Ni-Cu-PGE deposits at the base of the Sudbury Igneous Complex in Canada. The samples represent the crystallization products of fractionating sulfide liquids and consist of early-forming Fe-rich monosulfide solution (MSS) cumulates and residual Cu-rich intermediate solid solution (ISS). This study shows that Fe-oxide geochemistry is a sensitive petrogenetic indicator for the degree of fractionation of the sulfide liquid and provides an insight into the partitioning of elements between sulfide and Fe-oxide phases. In addition, it is useful in determining the provenance of detrital Fe-oxide. In a sulfide melt, all lithophile elements (Cr, Ti, V, Al, Mn, Sc, Nb, Ga, Ge, Ta, Hf, W and Zr) are compatible into Fe-oxide. The concentrations of these elements are highest in the early-forming Fe-oxide (titanomagnetite) which crystallized with Fe-rich MSS. Upon the continual crystallization of Fe-oxide from the sulfide liquid, the lithophile elements gradually decrease so that late-forming Fe-oxide (magnetite), which crystallized from the residual Cu-rich liquid, is depleted in these elements. This behavior is in contrast with Fe-oxides that crystallized from a fractionating silicate melt, whereby the concentration of incompatible elements, such as Ti, increases rather than decreases. The behavior of the chalcophile elements in magnetite is largely controlled by the crystallization of the sulfide minerals with only Ni, Co, Zn, Mo, Sn and Pb present above detection limit in magnetite. Nickel, Mo and Co are compatible in Fe-rich MSS and thus the co-crystallizing Fe-oxide is depleted in these elements. In contrast, magnetite that crystallized later from the fractionated liquid with Cu-rich ISS is enriched in Ni, Mo and Co because Fe-rich MSS is absent. The concentrations of Sn and Pb, which are incompatible with Fe-rich MSS, are highest in magnetite that formed from the fractionated Cu-rich liquid. At subsolidus temperatures, ilmenite exsolved from titanomagnetite whereas Al-spinel exsolved from the cores of some magnetite, locally redistributing the trace elements. However, during laser ablation ICP-MS analysis of these Fe-oxides both the magnetite and its exsolution products are ablated so that the analysis represents the original magmatic composition of the Fe-oxide that crystallized from the sulfide melt.

Determination of zircon/melt trace element partition coefficients from SIMS analysis of melt inclusions in zircon

NASA Astrophysics Data System (ADS)

Thomas, J. B.; Bodnar, R. J.; Shimizu, N.; Sinha, A. K.

2002-09-01

Partition coefficients ( zircon/meltD M) for rare earth elements (REE) (La, Ce, Nd, Sm, Dy, Er and Yb) and other trace elements (Ba, Rb, B, Sr, Ti, Y and Nb) between zircon and melt have been calculated from secondary ion mass spectrometric (SIMS) analyses of zircon/melt inclusion pairs. The melt inclusion-mineral (MIM) technique shows that D REE increase in compatibility with increasing atomic number, similar to results of previous studies. However, D REE determined using the MIM technique are, in general, lower than previously reported values. Calculated D REE indicate that light REE with atomic numbers less than Sm are incompatible in zircon and become more incompatible with decreasing atomic number. This behavior is in contrast to most previously published results which indicate D > 1 and define a flat partitioning pattern for elements from La through Sm. The partition coefficients for the heavy REE determined using the MIM technique are lower than previously published results by factors of ≈15 to 20 but follow a similar trend. These differences are thought to reflect the effects of mineral and/or glass contaminants in samples from earlier studies which employed bulk analysis techniques. D REE determined using the MIM technique agree well with values predicted using the equations of Brice (1975), which are based on the size and elasticity of crystallographic sites. The presence of Ce 4+ in the melt results in elevated D Ce compared to neighboring REE due to the similar valence and size of Ce 4+ and Zr 4+. Predicted zircon/meltD values for Ce 4+ and Ce 3+ indicate that the Ce 4+/Ce 3+ ratios of the melt ranged from about 10 -3 to 10 -2. Partition coefficients for other trace elements determined in this study increase in compatibility in the order Ba < Rb < B < Sr < Ti < Y < Nb, with Ba, Rb, B and Sr showing incompatible behavior (D M < 1.0), and Ti, Y and Nb showing compatible behavior (D M > 1.0). The effect of partition coefficients on melt evolution during petrogenetic modeling was examined using partition coefficients determined in this study and compared to trends obtained using published partition coefficients. The lower D REE determined in this study result in smaller REE bulk distribution coefficients, for a given mineral assemblage, compared to those calculated using previously reported values. As an example, fractional crystallization of an assemblage composed of 35% hornblende, 64.5% plagioclase and 0.5% zircon produces a melt that becomes increasingly more enriched in Yb using the D Yb from this study. Using D Yb from Fujimaki (1986) results in a melt that becomes progressively depleted in Yb during crystallization.

Accessory and rock forming minerals monitoring the evolution of zoned mafic ultramafic complexes in the Central Ural Mountains

NASA Astrophysics Data System (ADS)

Krause, J.; Brügmann, G. E.; Pushkarev, E. V.

2007-04-01

This study describes major and trace element compositions of accessory and rock forming minerals from three Uralian-Alaskan-type complexes in the Ural Mountains (Kytlym, Svetley Bor, Nizhnii Tagil) for the purpose of constraining the origin, evolution and composition of their parental melts. The mafic-ultramafic complexes in the Urals are aligned along a narrow, 900 km long belt. They consist of a central dunite body grading outward into clinopyroxenite and gabbro lithologies. Several of these dunite bodies have chromitites with platinum group element mineralization. High Fo contents in olivine (Fo 92-93) and high Cr/(Cr + Al) in spinel (0.67-0.84) suggest a MgO-rich (> 15 wt.%) and Al 2O 3-poor ultramafic parental magma. During its early stages the magma crystallized dominantly olivine, spinel and clinopyroxene forming cumulates of dunite, wehrlite and clinopyroxenite. This stage is monitored by a common decrease in the MgO content in olivine (Fo 93-86) and the Cr/(Cr + Al) value of coexisting accessory chromite (0.81-0.70). Subsequently, at subsolidus conditions, the chromite equilibrated with the surrounding silicates producing Fe-rich spinel while Al-rich spinel exsolved chromian picotite and chromian titanomagnetite. This generated the wide compositional ranges typical for spinel from Uralian-Alaskan-type complexes world wide. Laser ablation analyses (LA-ICPMS) reveal that clinopyroxene from dunites and clinopyroxenite from all three complexes have similar REE patterns with an enrichment of LREE (0.5-5.2 prim. mantle) and other highly incompatible elements (U, Th, Ba, Rb) relative to the HREE (0.25-2.0 prim. mantle). This large concentration range implies the extensive crystallization of olivine and clinopyroxene together with spinel from a continuously replenished, tapped and crystallizing magma chamber. Final crystallization of the melt in the pore spaces of the cooling cumulate pile explains the large variation in REE concentrations on the scale of a thin section, the REE-rich rims on zoned clinopyroxene phenocrysts (e.g. La Rim/La Core ˜ 2), and the formation of interstitial clinopyroxene with similar REE enrichment. Trace element patterns of the parental melt inferred from clinopyroxene analyses show negative anomalies for Ti, Zr, Hf, and a positive anomaly for Sr. These imply a subduction related geotectonic setting for the Uralian zoned mafic-ultramafic complexes. Ankaramites share many petrological and geochemical features with these complexes and could represent the parental melts of this class of mafic-ultramafic intrusions. Diopside from chromitites and cross cutting diopside veins in dunite has similar trace element patterns with LREE/HREE ratios (e.g. La/Lu = 5-60) much higher than those in diopside from all other lithologies. We suggest that the chromitites formed at high temperatures (800-900 °C) during the waning stages of solidification as a result of the interaction of an incompatible element-rich melt or fluid with the dunite cumulates.

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

DOE PAGES

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

2016-02-02

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

Orthopyroxene as a recorder of primitive achondrite petrogenesis: Major-, minor-, and trace-element systematics of orthopyroxene in Lodran. [Abstract only

NASA Technical Reports Server (NTRS)

Papike, J. J.; Spilde, M. N.; Fowler, G. W.; Shearer, C. K.

1994-01-01

Considerable attention has been paid recently to the primitive achondrites because they may form a link between chondrites and more differentiated achondrite meteorites. A recent paper by Miyamoto and Takeda addresses the thermal history of lodranites Yamato 74357 and MAC 88177 as inferred from chemical zoning of pyroxene and olivine determined by electron microprobe analyses. Their results suggested that interstitial melt was present and then extracted. We have taken the analysis of Lodran-type meteorites one step further by incorporating the techniques of Electromagnetic Pulse/Wavelength Dispersive Spectroscopy (EMP/WDS) compositional imaging and scanning ion mass spectroscopy (SIMS) analysis. Orthopyroxene in Lodran is strongly zoned in CaO, Al2O3, TiO2, and Cr2O3 within the last 10-30 microns from the grain boundaries. The rims are reversely zoned in Mg-Fe, exhibiting Mg enrichment, and compositions change from a fairly uniform Wo3En94 within the grains to Wo1En96 at the rims. CaO drops from 1.6 to 0.6 wt% and Al2O3, TiO2, and Cr2O3 exhibit similar depletions. MnO is fairly uniform throughout the grains at around 0.5 wt%. Olivine is also reversely zoned with respect to not only grain boundaries but also to fractures within the grains, giving many olivine grains a complex, patchy zoning pattern. Some of the core-rim trace-element systematics for orthopyroxene are illustrated. Because of the rather narrow zoned rims in Lodran orthopyroxene and the low trace-element abundances, it is difficult to clearly resolve the trace-element systematics. Nevertheless it is evident that the cores are enriched in the incompatible trace elements Ce, Nd, Dy, Er, Yb, Y, and Zr relative to the rims.

Derivation of Apollo 14 High-Al Basalts from Distinct Source Regions at Discrete Times: New Constraints

NASA Technical Reports Server (NTRS)

Neal, C. R.; Shih, C.-Y.; Reese, Y.; Nyquist, L. E.; Kramer, G. Y.

2006-01-01

Apollo 14 basalts occur predominantly as clasts in breccias, but represent the oldest volcanic products that were returned from the Moon [1]. These basalts are relatively enriched in Al2O3 (11-16 wt%) compared to other mare basalts (7-11 wt%) and were originally classified into 5 compositional groups [2,3]. Neal et al. [4] proposed that a continuum of compositions existed. These were related through assimilation (of KREEP) and fractional crystallization (AFC). Age data, however, show that at least three volcanic episodes are recorded in the sample collection [1,5,6]. Recent work has demonstrated that there are three, possibly four groups of basalts in the Apollo 14 sample collection that were erupted from different source regions at different times [7]. This conclusion was based upon incompatible trace element (ITE) ratios of elements that should not be fractionated from one another during partial melting (Fig. 1). These groups are defined as Group A (Groups 4 & 5 of [3]), Group B (Groups 1 & 2 of [3]), and Group C (Group 3 of [3]). Basalt 14072 is distinct from Groups A-C.

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.

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.

Efficiency of differentiation in the Skaergaard magma chamber

NASA Astrophysics Data System (ADS)

Tegner, C.; Lesher, C. E.; Holness, M. B.; Jakobsen, J. K.; Salmonsen, L.; Humphreys, M.; Thy, P.

2011-12-01

Although it is largely agreed that crystallization occurs inwardly in crystal mushes along the margins of magma chambers, the efficiency and mechanisms of differentiation are not well constrained. The fractionation paradigm hinges on mass exchange between the crystal mush and the main magma reservoir resulting in coarse-grained, refractory (cumulate) rocks of primary crystals, and complementary enrichment of incompatible elements in the main reservoir of magma. Diffusion, convection, liquid immiscibility and compaction have been proposed as mechanisms driving this mass exchange. Here we examine the efficiency of differentiation in basaltic crystal mushes in different regions of the Skaergaard magma chamber. The contents of incompatible elements such as phosphorus and calculated residual porosities are high in the lowermost cumulate rocks of the floor (47-30%) and decrease upsection, persisting at low values in the uppermost two-thirds of the floor rock stratigraphy (~5% residual porosity). The residual porosity is intermediate at the walls (~15%) and highest and more variable at the roof (10-100%). This is best explained by compaction and expulsion of interstitial liquid from the accumulating crystal mush at the floor and the inefficiency of these processes elsewhere in the intrusion. In addition, the roof data imply upwards infiltration of interstitial liquid. Remarkably uniform residual porosity of ~15% for cumulates formed along the walls suggest that their preservation is related to the rheological properties of the mush, i.e. at ≤ 15% porosity the mush is rigid enough to adhere to the wall, while at higher porosity it is easily swept away. We conclude that the efficiency of compaction and differentiation can be extremely variable along the margins of magma chambers. This should be taken into account in models of magma chamber evolution.

The Chlorine Isotopic Composition Of Lunar UrKREEP

NASA Technical Reports Server (NTRS)

Barnes, J. J.; Tartese, R.; Anand, M.; McCubbin, F. M.; Neal, C. R.; Franchi, I. A.

2016-01-01

Since the long standing paradigm of an anhydrous Moon was challenged there has been a renewed focus on investigating volatiles in a variety of lunar samples. Numerous studies have examined the abundances and isotopic compositions of volatiles in lunar apatite, Ca5(PO4)3(F,Cl,OH). In particular, apatite has been used as a tool for assessing the sources of H2O in the lunar interior. However, current models for the Moon's formation have yet to fully account for its thermal evolution in the presence of H2O and other volatiles. For ex-ample, in the context of the lunar magma ocean (LMO) model, it is anticipated that chlorine (and other volatiles) should have been concentrated in the late-stage LMO residual melts (i.e., the dregs enriched in incompatible elements such as K, REEs (Rare Earth Elements), and P, collectively called KREEP, and in its primitive form - urKREEP, given its incompatibility in mafic minerals like olivine and pyroxene, which were the dominant phases that crystallized early in the cumulate pile of the LMO. When compared to chondritic meteorites and terrestrial rocks, lunar samples have exotic chlorine isotope compositions, which are difficult to explain in light of the abundance and isotopic composition of other volatile species, especially H, and the current estimates for chlorine and H2O in the bulk silicate Moon (BSM). In order to better understand the processes involved in giving rise to the heavy chlorine isotope compositions of lunar samples, we have performed a comprehensive in situ high precision study of chlorine isotopes in lunar apatite from a suite of Apollo samples covering a range of geochemical characteristics and petrologic types.

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.

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.

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.

Zinc, copper, and lead in mid-ocean ridge basalts and the source rock control on Zn/Pb in ocean-ridge hydrothermal deposits

USGS Publications Warehouse

Doe, B.R.

1994-01-01

The contents of Zn, Cu, and Pb in mid-ocean ridge basalts (MORB) and the MORB source-rock control on Zn/Pb in ocean-ridge hydrothermal deposits are examined. The values of Zn, Cu, and Pb for submarine mid-ocean ridge basalts (MORB) are, respectively (in ppm): average MORB-75, 75, and 0.7; West Valley, Juan de Fuca Ridge (JFR)-87, 64, and 0.5; southern JFR-120 and 0.5; and 21??N, East Pacific Rise (EPR)-73, 78, and 0.5. Values of Zn/Pb range from about 100-240 and Cu/ Pb from 100-156. In this study, Zn is found to correlate positively with TiO2 + FeO (mean square of weighted deviates, MSWD, of 1.6 for JFR basalt), and inversely with Mg number (MSWD of 3.5). Therefore, contrary to statements in the literature that Zn should be compatible in MORB, Zn is a mildly incompatible element and must be enriched in the glass phase relative to olivine as Zn does not fit into the other major phenocryst phase, plagioclase. In the source of MORB, Zn likely is most enriched in oxides: spinel, magnetite, and titanomagnetite. Copper generally does not correlate well with other elements in most MORB data examined. When differentiation is dominated by olivine, Cu has a tendency to behave incompatibly (e.g., at Mg numbers > 70), but, overall, Cu shows some tendency towards being a compatible element, particularly along the Mid-Atlantic Ridge, a behavior presumably due to separation of sulfides in which Cu (but not Zn) is markedly enriched. Copper thus may be in dispersed sulfides in the source of MORB. Ocean ridges provide important data on source-rock controls for sulfide deposits because, in sediment-starved ridges, much is known about the possible source rocks and mineralization is presently occurring. In contrast to Zn/Pb ~5 in continental hot Cl-rich brines, Zn/Pb in the hottest sediment-starved ridge black smoker hydrothermal fluids at 21 ??N, EPR is about 110, similar to local MORB (145), but Cu/Pb is closer to 30, possibly due to subsurface deposition of Cu. At the JFR, the best value of Zn/Pb in the hydrothermal fluids is about 175, again similar to local MORB (240), but Cu is very low in the fluids that are at temperatures less than 300??C. The large MORB-like Zn/Pb in the hottest black-smoker fluids suggests a source-rock control for the metals that prohibits significant galena in the black-smoker deposits of sediment-starved ridges. In contrast, exhalative deposits on sediment-swamped ridges have significant galena; its presence is suggestive of Pb derivation from sediments, an origin supported by Pb isotope studies of LeHuray and colleagues in 1988. ?? 1994.

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.

Experimental determination of C, F, and H partitioning between mantle minerals and carbonated basalt, CO2/Ba and CO2/Nb systematics of partial melting, and the CO2 contents of basaltic source regions

NASA Astrophysics Data System (ADS)

Rosenthal, A.; Hauri, E. H.; Hirschmann, M. M.

2015-02-01

To determine partitioning of C between upper mantle silicate minerals and basaltic melts, we executed 26 experiments between 0.8 and 3 GPa and 1250-1500 °C which yielded 37 mineral/glass pairs suitable for C analysis by secondary ion mass spectrometry (SIMS). To enhance detection limits, experiments were conducted with 13C-enriched bulk compositions. Independent measurements of 13C and 12C in coexisting phases produced two C partition coefficients for each mineral pair and allowed assessment of the approach to equilibrium during each experiment. Concentrations of C in olivine (ol), orthopyroxene (opx), clinopyroxene (cpx) and garnet (gt) range from 0.2 to 3.5 ppm, and resulting C partition coefficients for ol/melt, opx/melt, cpx/melt and gt/melt are, respectively, 0.0007 ± 0.0004 (n = 2), 0.0003 ± 0.0002 (n = 45), 0.0005 ± 0.0004 (n = 17) and 0.0001 ± 0.00007 (n = 5). The effective partition coefficient of C during partial melting of peridotite is 0.00055 ± 0.00025, and therefore C is significantly more incompatible than Nb, slightly more compatible than Ba, and, among refractory trace elements, most similar in behavior to U or Th. Experiments also yielded partition coefficients for F and H between minerals and melts. Combining new and previous values of DFmineral/melt yields bulk DFperidotite/melt = 0.011 ± 0.002, which suggests that F behaves similarly to La during partial melting of peridotite. Values of DHpyx/melt correlate with tetrahedral Al along a trend consistent with previously published determinations. Small-degree partial melting of the mantle results in considerable CO2/Nb fractionation, which is likely the cause of high CO2/Nb evident in some Nb-rich oceanic basalts. CO2/Ba is much less easily fractionated, with incompatible-element-enriched partial melts having lower CO2/Ba than less enriched basalts. Comparison of calculated behavior of CO2, Nb, and Ba to systematics of oceanic basalts suggests that depleted (DMM-like) sources have 75 ± 25 ppm CO2 (CO2/Nb = 505 ± 168, CO2/Ba = 133 ± 44), whereas enriched sources of intraplate basalts similar in concentrations to primitive mantle have 600 ± 200 ppm CO2. If all mantle reservoirs are expressed in the current inventory of oceanic basalts for which nearly undegassed CO2 concentrations are available, then we estimate the likely range of mantle C concentrations to be 1.4-4.8 × 1023 grams of C, or 1.5-5.2 times the mass of the current C surface reservoir. Depending on the assumed Ba and Nb contents of average oceanic crust, resulting ridge fluxes of C range from 7.2 × 1013 to 2.9 × 1014 g/yr.

Submarine sliver in North Kona: A window into the early magmatic and growth history of Hualalai Volcano, Hawaii

USGS Publications Warehouse

Hammer, Julia E.; Coombs, Michelle L.; Shamberger, Patrick J.; Kimura, Jun-Ichi

2006-01-01

Sulfur-rich hawaiite glasses at the base of the elongate ridge may represent the first extant representatives of juvenile alkalic volcanism at Hualalai. They are geochemically distinct from shield tholeiite and post-shield alkalic magmas, but may be related to transitional basalt by high-pressure crystal fractionation of clinopyroxene. Tholeiitic glasses that compose the majority of the exposed outcrop are similar to Mauna Kea tholeiites and other Hualalai tholeiites, but they differ from younger basalts in having greater incompatible element enrichments and higher CaO for a given MgO. These differences could arise from small extents of partial melting during the transition from alkalic to shield stage magmatism. Low sulfur contents of most of the volcaniclastic tholeiites point to early emergence of Hualalai above sea level relative to the development of the midslope slump bench.

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

NASA Astrophysics Data System (ADS)

Schiano, P.; Clocchiatti, R.

1994-04-01

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

Reduced sediment melting at 7.5-12 GPa: phase relations, geochemical signals and diamond nucleation

NASA Astrophysics Data System (ADS)

Brey, G. P.; Girnis, A. V.; Bulatov, V. K.; Höfer, H. E.; Gerdes, A.; Woodland, A. B.

2015-08-01

Melting of carbonated sediment in the presence of graphite or diamond was experimentally investigated at 7.5-12 GPa and 800-1600 °C in a multianvil apparatus. Two starting materials similar to GLOSS of Plank and Langmuir (Chem Geol 145:325-394, 1998) were prepared from oxides, carbonates, hydroxides and graphite. One mixture (Na-gloss) was identical in major element composition to GLOSS, and the other was poorer in Na and richer in K (K-gloss). Both starting mixtures contained ~6 wt% CO2 and 7 wt% H2O and were doped at a ~100 ppm level with a number of trace elements, including REE, LILE and HFSE. The near-solidus mineral assemblage contained a silica polymorph (coesite or stishovite), garnet, kyanite, clinopyroxene, carbonates (aragonite and magnesite-siderite solid solution), zircon, rutile, bearthite and hydrous phases (phengite and lawsonite at <9 GPa and the hydrous aluminosilicates topaz-OH and phase egg at >10 GPa). Hydrous phases disappear at ~900 °C, and carbonates persist up to 1000-1100 °C. At temperatures >1200 °C, the mineral assemblage consists of coesite or stishovite, kyanite and garnet. Clinopyroxene stability depends strongly on the Na content in the starting mixture; it remains in the Na-gloss composition up to 1600 °C at 12 GPa, but was not observed in K-gloss experiments above 1200 °C. The composition of melt or fluid changes gradually with increasing temperature from hydrous carbonate-rich (<10 wt% SiO2) at 800-1000 °C to volatile-rich silicate liquids (up to 40 wt% SiO2) at high temperatures. Trace elements were analyzed in melts and crystalline phases by LA ICP MS. The garnet-melt and clinopyroxene-melt partition coefficients are in general consistent with results from the literature for volatile-free systems and silicocarbonate melts derived by melting carbonated peridotites. Most trace elements are strongly incompatible in kyanite and silica polymorphs ( D < 0.01), except for V, Cr and Ni, which are slightly compatible in kyanite ( D > 1). Aragonite and Fe-Mg carbonate have very different REE partition coefficients ( D Mst-Sd/L ~ 0.01 and D Arg/L ~ 1). Nb, Ta, Zr and Hf are strongly incompatible in both carbonates. The bearthite/melt partition coefficients are very high for LREE (>10) and decrease to ~1 for HREE. All HFSE are strongly incompatible in bearthite. In contrast, Ta, Nb, Zr and Hf are moderately to strongly compatible in ZrSiO4 and TiO2 phases. Based on the obtained partition coefficients, the composition of a mobile phase derived by sediment melting in deep subduction zones was calculated. This phase is strongly enriched in incompatible elements and displays a pronounced negative Ta-Nb anomaly but no Zr-Hf anomaly. Although all experiments were conducted in the diamond stability field, only graphite was observed in low-temperature experiments. Spontaneous diamond nucleation and the complete transformation of graphite to diamond were observed at temperatures above 1200-1300 °C. We speculate that the observed character of graphite-diamond transformation is controlled by relationships between the kinetics of metastable graphite dissolution and diamond nucleation in a hydrous silicocarbonate melt that is oversaturated in C.

A new Mantle Source Tapped During Episode 55 of the Pu'u O'o Eruption From Kilauea Volcano

NASA Astrophysics Data System (ADS)

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

2005-12-01

Over 22 years of continuous geochemical monitoring of lavas from the current Pu'u O'o eruption allows us to probe the mantle and crustal processes beneath Kilauea Volcano in unparalleled detail. Episode 55 (1997-present) marks the longest and most voluminous Pu'u O'o eruptive interval. Here we present new Pb, Sr, and Nd isotopic ratios and major- and trace-element abundances for the most recent lavas (1999-2005). MgO variation diagrams show that most of the major-element variations are related to olivine fractionation. However, Pu'u O'o lavas display longer-term systematic decreases in their TiO2, K2O, P2O5 and CaO abundances (at a given MgO) due to changes in the parental magma composition. Incompatible element ratios (K2O/TiO2, Nb/Y, Nb/Zr) and MgO-normalized abundances (Sr, Rb, K) in episode 55 lavas delimit the lowest values observed during the Pu'u O'o eruption. Earlier Pu'u O'o lavas displayed a temporal decrease in highly over moderately incompatible trace-element ratios, near constant SiO2 contents, and a gradual increase in 87Sr/86Sr. However, episode 55 lavas (between days 5500-6500) record an increase in MgO-normalized SiO2 contents and even higher 87Sr/86Sr with near constant incompatible trace-element ratios. Neither a single mantle source composition nor a change in partial melting conditions can explain these observations. Based on 226Ra-230Th-238U disequilibria and partial melting modeling of trace elements, we conclude that Pu'u O'o lavas originate from at least two distinct mantle source components: (1) a recently depleted component that was subsequently remelted to explain the overall decreases of incompatible major- and trace-element ratios and abundances, and (2) a compositionally and isotopically distinct mantle component that was not previously melted within the Hawaiian plume to explain the temporal increase in 87Sr/86Sr and SiO2 abundances and the flattening trend of incompatible trace-element ratios. This second 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. These results can be explained by a recent (1999) change in the size or location of Pu'u O'o's melting region, which allowed this new source to be tapped.

Crystallization conditions and controls on trace element residence in the main minerals from the Pedra Branca Syenite, Brazil: An electron microprobe and LA-ICPMS study

NASA Astrophysics Data System (ADS)

Carvalho, Bruna Borges; Janasi, Valdecir de Assis

2012-11-01

Major and trace-element microanalyses of the main minerals from the 610 Ma Pedra Branca Syenite, southeast Brazil, allow inferences on intensive parameters of magmatic crystallization and on the partition of trace-elements among these minerals, with important implications for the petrogenetic evolution of the pluton. Two main syenite types make up the pluton, a quartz-free syenite with tabular alkali feldspar (laminated silica-saturated syenite, LSS, with Na-rich augite + phlogopite + hematite + magnetite + titanite + apatite) and a quartz-bearing syenite (laminated silica-oversaturated syenite, LSO, with scarce corroded plagioclase plus diopside + biotite ± hornblende + ilmenite ± magnetite + titanite + apatite). Both types share a remarkable enrichment in incompatible elements as K, Ba, Sr, P and LREE. Apatite saturation temperatures of ~ 1060-1090 °C are the best estimates of liquidus, whereas the pressure of emplacement, based on Al-in-hornblende barometry, is estimated as 3.3 to 4.8 kbar. Although both units crystallized under oxidizing conditions, oxygen fugacity was probably higher in LSS, as shown by higher mg# of the mafic minerals and higher hematite contents in Hem-Ilmss. In contrast with the Ca-bearing alkali-feldspar from LSO, which hosts most of the whole-rock Sr and Pb, virtually Ca-free alkali-feldspar from LSS hosts ~ 50% of whole-rock Sr and ~ 80% of Pb, the remainder of these elements being shared by apatite, pyroxene and titanite. This contrast reflects a strong crystal-chemical control, whereby a higher proportion of an element with similar ratio and charge (Ca2 +) enhances the residence of Sr and Pb in the M-site of alkali feldspar. The more alkaline character of the LSS magma is inferred to have inhibited zircon saturation; Zr + Hf remained in solution until late in the crystallization, and were mostly accommodated in the structure of Ca-Na pyroxene and titanite, which are one order of magnitude richer in these elements compared to the same minerals in LSO, where most of Zr and Hf are inferred to reside in zircon. The REE, Th and U reside mostly in titanite and apatite; D(REE)Tit/Ap raises steadily from 1 to 6 from La to Tb then remains constant up to Lu in the LSO sample; these values are about half as much in the LSS sample, where lower contents of incompatible elements in titanite are attributed to its greater modal abundance and earlier crystallization.

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.

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.

The nakhlite meteorites: Augite-rich igneous rocks from Mars

NASA Technical Reports Server (NTRS)

Treiman, Allan H.

2005-01-01

The seven nakhlite meteorites are augite-rich igneous rocks that formed in flows or shallow intrusions of basaltic magma on Mars. They consist of euhedral to subhedral crystals of augite and olivine (to 1 cm long) in fine-grained mesostases. The augite crystals have homogeneous cores of Mg' = 63% and rims that are normally zoned to iron enrichment. The core-rim zoning is cut by iron-enriched zones along fractures and is replaced locally by ferroan low-Ca pyroxene. The core compositions of the olivines vary inversely with the steepness of their rim zoning - sharp rim zoning goes with the most magnesian cores (Mg' = 42%), homogeneous olivines are the most ferroan. The olivine and augite crystals contain multiphase inclusions representing trapped magma. Among the olivine and augite crystals is mesostasis, composed principally of plagioclase and/or glass, with euhedra of titanomagnetite and many minor minerals. Olivine and mesostasis glass are partially replaced by veinlets and patches of iddingsite, a mixture of smectite clays, iron oxy-hydroxides and carbonate minerals. In the mesostasis are rare patches of a salt alteration assemblage: halite, siderite, and anhydrite/ gypsum. The nakhlites are little shocked, but have been affected chemically and biologically by their residence on Earth. Differences among the chemical compositions of the nakhlites can be ascribed mostly to different proportions of augite, olivine, and mesostasis. Compared to common basalts, they are rich in Ca, strongly depleted in Al, and enriched in magmaphile (incompatible) elements, including the LREE. Nakhlites contain little pre-terrestrial organic matter. Oxygen isotope ratios are not terrestrial, and are different in anhydrous silicates and in iddingsite. The alteration assemblages all have heavy oxygen and heavy carbon, while D/H values are extreme and scattered. Igneous sulfur had a solar-system isotopic ratio, but in most minerals was altered to higher and lower values. High precision analyses show mass-independent fractionations of S isotopes. Nitrogen and noble gases are complex and represent three components: two mantle sources (Chas-E and Chas-S), and fractionated Martian atmosphere. The nakhlites are igneous cumulate rocks, formed from basaltic magma at approx.1.3 Ga, containing excess crystals over what would form from pure magma. After accumulation of their augite and olivine crystals, they were affected (to various degrees) by crystallization of the magma, element diffusion among minerals and magma, chemical reactions among minerals and magma, magma movement among the crystals, and post-igneous chemical equilibration. The extent of these modifications varies, from least to greatest, in the order: MIL03346, NWA817, Y000593, Nakhla = Governador Valadares, Lafayette, and NWA998. Chemical, isotopic, and chronologic data confirm that the nakhlites formed on Mars, most likely in thick lava flows or shallow intrusions. Their crystallization ages, referenced to crater count chronologies for Mars, suggest that the nakhlites formed on the large volcanic constructs of Tharsis, Elysium, or Syrtis Major. The nakhlites were suffused with liquid water, probably at approx.620 ma. This water dissolved olivine and mesostasis glass, and deposited iddingsite and salt minerals in their places. The nakhlites were ejected from Mars at approx.10.75Ma by an asteroid impact and fell to Earth within the last 10,000 years. Although the nakhlites are enriched in incompatible elements, their source mantle was strongly depleted. This depletion event was ancient, as the nakhlites source mantle was fractionated while short-lived radionuclides (e.g., t(sub 1/2 = 9 my) were still active. This differentiation event may have been core formation coupled with a magma ocean, as is inferred for the moon.

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.

On the Interconnection of Incompatible Solid Finite Element Meshes Using Multipoint Constraints

NASA Technical Reports Server (NTRS)

Fox, G. L.

1985-01-01

Incompatible meshes, i.e., meshes that physically must have a common boundary, but do not necessarily have coincident grid points, can arise in the course of a finite element analysis. For example, two substructures may have been developed at different times for different purposes and it becomes necessary to interconnect the two models. A technique that uses only multipoint constraints, i.e., MPC cards (or MPCS cards in substructuring), is presented. Since the method uses only MPC's, the procedure may apply at any stage in an analysis; no prior planning or special data is necessary.

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

USGS Publications Warehouse

Tatsumoto, M.; Nakamura, Y.

1991-01-01

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

Mineral chemistry of magnetite from magnetite-apatite mineralization and their host rocks: examples from Kiruna, Sweden, and El Laco, Chile

NASA Astrophysics Data System (ADS)

Broughm, Shannon G.; Hanchar, John M.; Tornos, Fernando; Westhues, Anne; Attersley, Samuel

2017-12-01

Interpretation of the mineralizing environment of magnetite-apatite deposits remains controversial with theories that include a hydrothermal or magmatic origin or a combination of those two processes. To address this controversy, we have analyzed the trace element content of magnetite from precisely known geographic locations and geologic environments from the Precambrian magnetite-apatite ore and host rocks in Kiruna, Sweden, and the Pliocene-Holocene El Laco volcano in the Atacama desert of Chile. Magnetite samples from Kiruna have low trace element concentrations with little chemical variation between the ore, host, and related intrusive rocks. Magnetite from andesite at El Laco, and dacite from the nearby Láscar volcano, has high trace element concentrations typical of magmatic magnetite. El Laco ore magnetite have low trace element concentrations and displays growth zoning in incompatible elements (Si, Ca, and Ce), compatible elements (Mg, Al, and Mn), large-ion lithophile element (Sr), and high field strength element (Y, Nb, and Th). The El Laco ore magnetite are similar in composition to magnetite that has been previously interpreted to have crystallized from hydrothermal fluids; however, there is a significant difference in the internal zoning patterns. At El Laco, each zoned element is either enriched or depleted in the same layers, suggesting the magnetite crystallized from a volatile-rich, iron-oxide melt. In general, the compositions of magnetite from these two deposits plot in very wide fields that are not restricted to the proposed fields in published discriminant diagrams. This suggests that the use of these diagrams and genetic models based on them should be used with caution.

Decoupling of the Assimilation and Fractionation Signatures in a MASH Zone: Evidence from the Sierra Valle Fértil Mafic Zone, Argentina

NASA Astrophysics Data System (ADS)

Walker, B. A., Jr.; Bergantz, G. W.; Otamendi, J.; Ducea, M. N.; Cristofolini, E.

2015-12-01

The Sierra Valle Fértil (SVF) in northern Argentina is a tilted Ordovician fossil arc complex with continuous exposure from paleodepths of ~10 km to ~30 km. The system is layered when viewed at a large scale: shallow, granodiorite plutons give way to a heterogeneous granodiorite-tonalite zone, which in turn grades into a gabbro-tonalite zone at the base of the section. A metapelitic country rock package is interlayered throughout the magmatic complex, allowing for determination of emplacement depths within the section. Our work focuses on the lowermost domain of the SVF, as it preserves what we consider to be a frozen example of a MASH zone. Here, dominant rock types are hornblende gabbronorite and tonalitie variants, which appear to be interfingered as dm- to 10s of m-scale sheets. Mappable ultramafic pods containing dunites, websterites, troctolites, and minor anorthosites are also present. Field relations are consistent with a complex series of intrusive events. Much of the SVF mafic zone compositional array can be modeled by fractional crystallization where the mafic rocks are cumulate assemblages and the intermediate rocks are the daughter magmas. Amphibole and, perhaps more importantly, Fe-Ti oxide crystallization are likely the principal agents of silica enrichment. Metapelitic rocks exposed throughout the SVF are likely the vestiges of a country rock package that was melted (or reacted) and incorporated into SVF magmas, but field and compositional evidence for assimilation is cryptic in the mafic zone. While isotopic data (Sr, Nd, O) seem to implicate crustal contributions to the SVF mafic zone, incompatible major and trace elements typically associated with an "assimilation signature" (e.g., K, Rb, Ba) are sparse. Such elements are abundant in the metapelites and in igneous rocks farther up section. We interpret this isotopic and elemental decoupling as a byproduct of prolonged MASH processes in the lower crust. A high temperature and an increasingly mafic environment likely resulted in the development of a crystal mush inhospitable to crustally contributed incompatible elements. Over time, these elements were thoroughly flushed out of the MASH zone via melt extraction. Isotopes, then, may be the only residual evidence of assimilation within the SVF mafic zone.

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.

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.

Motivational interviewing in permanent supportive housing: the role of organizational culture.

PubMed

van den Berk-Clark, Carissa; Patterson Silver Wolf, David A; Ramsey, Alex

2015-07-01

This study evaluated motivational interviewing (MI) in a permanent supportive housing agency. The agency's contradictory social service and business missions resulted in an incompatible organizational culture theorized to diminish MI's effectiveness. A combination of observational, interview, and archival data collected over 3 years were used to examine MI implementation within an incompatible supportive housing agency. Two major themes arose: how MI is used to categorize and change clients in permanent supportive housing and how worker-worker relationships affect MI implementation. The results suggest that within incompatible organizational environments, key elements of effective MI implementation are greatly weakened.

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.

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.

The influence of fluorine on phase relations and REE enrichment in alkaline magmas

NASA Astrophysics Data System (ADS)

Beard, C. D.; van Hinsberg, V.; Stix, J.; Wilke, M.

2017-12-01

Fluorine is a minor element in most magmas, but higher concentrations to wt% levels have been reported in alkaline systems, including those which host economic deposits of REE + HFSE1. Despite low abundance in most natural melts, fluorine has received great attention from the experimental community because it has a strong influence on melt structure, lowering melting points and drastically reducing viscosity. The effect of fluorine on element speciation has important implications for phase relations and the partitioning of trace elements between minerals and melts, thus metal enrichment processes in alkaline magmas. We have experimentally investigated the impact of fluorine on phase relations and partitioning of rare metals, the REE in particular, in evolved alkaline melts. Synthetic glasses of tephriphonolite to phonolite composition were doped with a wide range of elements at trace levels, and fluorine contents were varied from fluorine-free to 2.5 wt%. Experiments were performed water-saturated in an internally heated pressure vessel at 200 MPa with log fO2 at ca. QFM+1, which represents the intrinsic redox conditions of the setup. Charges were heated to super-liquidus conditions for 16 hours, cooled slowly (1˚C/min) to run temperature and subsequently equilibrated for at least 40 hours. Run products were analysed by EPMA and LA-ICP-MS. The experiments produce an equilibrium assemblage of sodic pyroxene, biotite, Fe-oxide, melt, fluid, ±K-feldspar, ±titanite, ±fluorite. Addition of fluorine markedly increases the mode of biotite, which initially buffers melt F content at low levels (< 0.2 wt%). Only in experiments with more than 0.6 wt% F do we observe a significant increase in the melt F-content. Here, fluorine decreases pyroxene/melt partitioning coefficients equally for all REE where pyroxene composition and P-T conditions are equivalent (ca. 1/2 with 0.6% F). We suggest that the formation of REE-F complexes in the melt2 lowers the availability of metals for incorporation into solid phases. An increasing fluorine content of the melt will thus make the REE progressively more incompatible and available for residual enrichment. 1. Vasyukova, O. & Williams-Jones, A. E. Geochim. Cosmochim. Acta 139, 110-130 (2014). 2. Ponader, C. W. & Brown Jr., G. E. Geochim. Cosmochim. Acta 53, 2905-2914 (1989).

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.

Lithospheric and Asthenospheric Contributions to Post-Collisional Volcanism in the Lesser Caucasus Mts (Armenia)

NASA Astrophysics Data System (ADS)

Sugden, P.; Savov, I. P.; Wilson, M.; Meliksetian, K.; Navasardyan, G.

2017-12-01

Continental collision zones remain the most enigmatic tectonic setting for volcanic activity on earth. The Lesser Caucasus Mts are host to widespread and unique intraplate volcanism, associated with the active Arabia-Eurasia continental collision. Volcanic products range from alkali basalts to rhyolites (including extensive ignimbrites), and occur as basaltic lava flow fields, large composite and shield volcanoes, and regions of distributed (mostly monogenetic) volcanism. Geomorphology, archaeology, and historical accounts suggest volcanic activity has extended in to the Holocene-historical period. The high quality of the exposures and the diversity of unaltered rock types makes Armenia an ideal natural laboratory for studying the sources of magmatism in an active continental collision zone. For the first time, we will present the mineral chemistry (ol, px, amph), whole rock major and trace element, and Sr-Nd isotope compositions of volcanic rocks from southernmost Armenia- namely the Gegham, Vardenis and Syunik volcanic highlands. We compare our dataset with the composition of post-collisional volcanic rocks elsewhere in the Arabia-Eurasia collision zone. Samples from S. Armenia are more mafic, more alkaline and more K2O rich. All volcanic rocks show negative HFSE anomalies and LILE and LREE enrichments reminiscent of continental volcanic arc settings. However, volcanic rocks in Southern Armenia are further enriched in some of the most incompatible trace elements, most notably LREE, Sr and P, and have higher La/Yb, Th/Yb, Ta/Yb, and more variable Th/Nb. Volcanic rocks from Eastern Anatolia and N. Armenia have Sr-Nd isotope compositions similar to those of the Mesozoic volcanic arc (87Sr/86Sr 0.7034-0.7045; 143Nd/144Nd 0.5128-0.5129), whereas samples from S. Armenia deviate towards more enriched compositions resembling a typical EM-I type reservoir (87Sr/86Sr 0.7041- 0.7047; 143Nd/144Nd 0.5127-0.5128). We argue that these distinctive geochemical characteristics result from the addition of an enriched lithospheric component to a ubiquitous subduction-modified baseline asthenospheric mantle. This EM-I like component may be characteristic for not only intraplate hotspot volcanoes but also to collisional and arc settings.

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

NASA Astrophysics Data System (ADS)

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

2009-06-01

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

Th-230 - U-238 series disequilibrium of the Olkaria rhyolites Gregory Rift Valley, Kenya: Petrogenesis

NASA Technical Reports Server (NTRS)

Black, S.; Macdonald, R.; Kelly, M.

1993-01-01

Positive correlations of (U-238/Th-230) versus Th show the rhyolites to be products of partial melting. Positive correlations of U and Cl and U and F show that the U enrichment in the rhyolites is associated with the halogen contents which may be related to the minor phenocryst phase fractionation. Instantaneous Th/U ratios exceed time integrated Th/U ratios providing further evidence of the hydrous nature of the Olkaria rhyolite source. Excess (U-238/Th-230) in the subduction related rocks has been associated to the preferential incorporation of uranium in slab derived fluids, but no evaluation of the size of this flux has been made. The majority of the Naivasha samples show a (U-238/Th-230) less than 1 and plot close to the subduction related samples indicating the Naivasha rhyolites may also have been influenced by fluids during their formation. In general samples with high (U-238/Th-230) ratios reflecting recent enrichment of uranium relative to thorium have high thorium contents, thereby the high (U-238/Th-230) ratios are restricted to the most incompatible element enriched magmas and, hence, are a good indication that the rhyolites were formed by partial melting. If a fluid phase had some influence on the formation of the rhyolites then the uranium and thorium may have some correlation with F and Cl contents which can be mirrored by the peralkalinity. Plots of uranium against F and Cl contents are shown. The positive correlation indicates that the uranium enrichments are associated with the halogen contents. There seems to be a greater correlation for U against Cl than F indicating that the U may be transported preferentially as Cl complexes.

A global geochemical model for the evolution of the mantle

NASA Technical Reports Server (NTRS)

Anderson, D. L.

1979-01-01

It is proposed that the upper mantle transition region, 220 to 670 km, is composed of eclogite which has been derived from primitive mantle by about 20 percent partial melting and that this is the source and sink of oceanic crust. The remainder of the upper mantle is garnet peridotite which is the source of continental basalts and hotspot magmas. This region is enriched in incompatible elements by hydrous and CO2 rich metasomatic fluids which have depleted the underlying layers in the L.I.L. elements and L.R.E.E. The volatiles make this a low-velocity, high attenuation, low viscosity region. The eclogite layer is internally heated and its controls the convection pattern in the upper mantle. Plate tectonics is intermittent. The continental thermal anomaly at a depth of 150-220 km triggers kimberlite and carbonatite activity, alkali and flood basalt volcanism, vertical tectonics and continental breakup. Hot spots remain active after the continents leave and build the oceanic islands. Mantle plumes rise from a depth of about 220 km. Midocean ridge basalts rise from the depleted layer below this depth. Material from this layer can also be displaced upwards by subducted oceanic lithosphere to form back-arc basins.

Magmatic (silicates/saline/sulfur-rich/CO2) immiscibility and zirconium and rare-earth element enrichment from alkaline magma chamber margins : Evidence from Ponza Island, Pontine Archipelago, Italy

USGS Publications Warehouse

Belkin, H.E.; de Vivo, B.; Lima, A.; Torok, K.

1996-01-01

Fluid inclusions were measured from a feldspathoid-bearing syenite xenolith entrained in trachyte from Ponza, one of the islands of the Pontine Archipelago, located in the Gulf of Gaeta, Italy. The feldspathoid-bearing syenite consists mainly of potassium feldspar, clinopyroxene, amphibole, biotite, titanite, manganoan magnetite, apatite with minor nosean, Na-rich feldspar, pyrrhotite, and rare cheralite. Baddeleyite and zirkelite occur associated with manganoan magnetite. Detailed electron-microprobe analysis reveals enrichments in REE, Y, Nb, U, Th as well as Cl and F in appropriate phases. Fluid inclusions observed in potassium feldspar are either silicate-melt or aqueous inclusions. The aqueous inclusions can be further classified as. (1) one-phase vapor, (2) two-phase (V + L) inclusions, vapor-rich inclusions with a small amount of CO2 in most cases; homogenization of the inclusions always occurred in the vapor phase between 359 and 424??C, salinities vary from 2.9 to 8.5 wt. % NaCl equivalent; and. (3) three-phase and multiphase inclusions (hypersaline/sulfur-rich aqueous inclusions sometimes with up to 8 or more solid phases). Daughter minerals dissolve on heating before vapor/liquid homogenization. Standardless quantitative scanning electron microscope X-ray fluorescence analysis has tentatively identified the following chloride and sulfate daughter crystals; halite, sylvite, glauberite. arcanite, anhydrite, and thenardite. Melting of the daughter crystals occurs between 459 and 536??C (54 to 65 wt. % NaCI equivalent) whereas total homogenization is between 640 and 755??C. The occurrence of silicate-melt inclusions and high-temperature, solute-rich aqueous inclusions suggests that the druse or miarolitic texture of the xenolith is late-stage magmatic. The xenolith from Ponza represents a portion of the peripheral magma chamber wall that has recorded the magmatic/hydrothermal transition and the passage of high solute fluids enriched in chlorides, sulfur, and incompatible elements.

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.

Constraining magma ascent and degassing paths with olivine- and clinopyroxene-hosted melt inclusions: Evidence for multiple depths of crystallization and boundary-layer entrapment

NASA Astrophysics Data System (ADS)

Lloyd, A. S.; Newcombe, M. E.; Plank, T. A.

2016-12-01

Although olivine-hosted melt inclusions (MIs) remain the gold standard for recovering volatile concentrations of primitive magmas, later-fractionating minerals may be more appropriate for assessing magma storage conditions immediately prior to eruption. We present volatile analyses of MIs entrapped in early (Mg# 81-83) olivine and later (Mg# 70-80) clinopyroxene (Cpx) from the 1977 eruption of Seguam volcano, to assess the ascent history prior to this violent strombolian eruption. The olivine-hosted MIs contain average volatile concentrations (n=16) of 3.79 wt% H2O, 167 ppm CO2, 592 ppm Cl, and 133 ppm F, consistent with an entrapment pressure of 200 to 300 MPa ( 10-13 km depth) if the CO2 contained in the bubble is taken into account (Moore et al., 2015). Cpx phenocrysts contain two distinct MI assemblages; the inner assemblage consists of randomly distributed, rounded MIs which never contain a vapor bubble. Average volatile concentrations of the inner assemblage MIs (n=11) are 0.96 wt% H2O, 98 ppm CO2, 798 ppm Cl, and 280 ppm F, consistent with an entrapment at much shallower depth, 2 km. The outer assemblage contains inclusions too small for routine volatile analysis. Inner assemblage Cpx-hosted MIs preserve average enrichments of 1.3x and 2x for Cl and F respectively, and are similarly enriched in incompatible minor and trace elements (up to a factor of 5x). Two potential scenarios can explain these observations. The enrichments may represent the entrapment of an unrelated highly-fractionated, shallow magma (which is unsupported by the whole rock record at Seguam). A second possibility is enrichment through boundary layer entrapment during a period of rapid crystal growth during ascent through the upper crust. Boundary layer entrapment during MI formation is further supported by a negative correlation between the degree of enrichment and the diffusivity of individual elements, which is consistent with growth rates 10-8 m/s. Although the olivine-hosted MIs record a volatile-rich storage region, the later-fractionating Cpx indicate a phase of rapid crystallization, likely driven by water loss from the melt at shallow depths. This work highlights the information added by analyzing multiple phases in order to reconstruct the degassing path of magma prior to eruption.

Geochemical characteristics of aluminum depleted and undepleted komatiites and HREE-enriched low-Ti tholeiites, western Abitibi greenstone belt: A heterogeneous mantle plume-convergent margin environment

NASA Astrophysics Data System (ADS)

Fan, J.; Kerrich, R.

1997-11-01

A compositionally diverse suite of komatiites, komatiitic basalts, and basalts coexist in the Tisdale volcanic assemblage of the late-Archean (˜2.7 Ga) Abitibi greenstone belt. The komatiites are characterized by a spectrum of REE patterns, from low total REE contents (9 ppm) and pronounced convex-up patterns to greater total REE (18 ppm) and approximately flat-distributions. Thorium and niobium are codepleted with LREE. Komatiites with the most convex-up patterns have low Al 2O 3 (4.7 wt%) contents and Al 2O 3/TiO 2(12) ratios; they are interpreted to be the Al-depleted variety of komatiite derived from a depleted mantle source. Those komatiites and komatiitic basalts with flatter REE patterns are characterized by greater Al 2O 3 (7.0 wt%) and near chondritic Al 2O 3/TiO 2 (20) ratios; they are interpreted to be Al-undepleted komatiites generated from trace element undepleted mantle. For the komatiites and komatiitic basalts collectively, Gd/Ybn ratios are negatively correlated with La/Smn, but positively with MgO and Ni. The spectrum of patterns is interpreted as mixing between Al, HREE, Y-depleted, and Sc-depleted komatiites and Al-undepleted komatiites in a heterogeneous mantle plume. Auminum-depleted komatiites are characterized by negative Zr and Hf anomalies, consistent with majorite garnet-liquid D's for HFSE and REEs, signifying melt segregation at depths of >400 km. Tisdale Al-undepleted komatiites and komatiitic basalts have small negative to zero Zr(Hf)/MREE fractionation, signifying melt segregation in or above the garnet stability field. Collectively, the komatiites have correlations of Zr/Zr∗ and Hf/Hf ∗ with Gd/Ybn, and hence the Zr(Hf)/MREE fractionations are unlikely to have stemmed from alteration or crustal contamination. Two types of basalts are present. Type I basalts are Mg-tholeiites with near flat REE and primitive mantle normalized patterns, compositionally similar to abundant Mg-tholeiites associated with both Al-undepleted and Al-depleted komatiites in the Abitibi belt. They have absolute concentrations and ratios of most moderately and highly compatible elements comparable to N- MORB (Zr ˜79 vs. 74, Y ˜30 vs. 28, and Zr/Y = 2.4-2.9 vs. 2.6 ), but are relatively less depleted in highly incompatible elements and lack positive Nb or P anomalies. Type II basalts are relatively aluminous (Al 2O 3 ˜ 16 wt%), with high Al 2O 3/TiO 2 (24-28) ratios. They are characterized by low Th, Nb, and LREE contents at eight to ten times chondrite, with slightly convex-up LREE patterns ( La/Smn = 0.86-0.99 ), but strongly fractionated and enriched HREEs, Y, and Sc, where Gd/Ybn = 0.50-0.55 and consistently positive Zr(Hf)/MREEs anomalies. These basalts are tentatively interpreted as low-Ti tholeiites formed in a convergent margin setting with second stage melting, induced by fluids and melts enriched in incompatible elements and Zr(Hf) relative to MREEs, of a mantle source depleted during first stage melting. They are analogous to the Phanerozoic low-Ti tholeiite - boninite association. Accordingly the Tisdale volcanic sequence records a plume-convergent margin interaction. New analyses of Al-undepleted komatiites from the classical locality at Pyke Hill in Munro Township confirm the presence of small positive anomalies of P, Zr, and Hf, with Zr/Hf ratios generally < 36. These signatures are similar in spinifex and cumulate zones signifying that they are unlikely to have resulted from alteration. The data were generated by INAA and ICP-MS using both HFHNO 3 dissolution and Na 2O 2 sinter. The lack of LREE enrichment with negative Nb, Ta, P, and Ti anomalies in any of the Tisdale or Munro komatiites confirms an intraoceanic setting for the volcanic stage of the Western Abitibi greenstone belt.

Motivational Interviewing in permanent supportive housing: The role of organizational culture

PubMed Central

van den Berk-Clark, Carissa; Patterson Silver Wolf (Adelv unegv Waya), David A.; Ramsey, Alex

2014-01-01

This study evaluated motivational interviewing (MI) in a permanent supportive housing agency. The agency’s contradictory social service and business missions resulted in an incompatible organizational culture theorized to diminish MI’s effectiveness. A combination of observational, interview, and archival data collected over 3 years were used to examine MI implementation within an incompatible supportive housing agency. Two major themes arose: how MI is used to categorize and change clients in permanent supportive housing and how worker–worker relationships affect MI implementation. The results suggest that within incompatible organizational environments, key elements of effective MI implementation are greatly weakened. PMID:25129815

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

NASA Astrophysics Data System (ADS)

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

2016-12-01

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

Evidence for lateral mantle plume flow feeding the Central Indian Ridge

NASA Astrophysics Data System (ADS)

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

2003-04-01

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

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.

Thermal breeder fuel enrichment zoning

DOEpatents

Capossela, Harry J.; Dwyer, Joseph R.; Luce, Robert G.; McCoy, Daniel F.; Merriman, Floyd C.

1992-01-01

A method and apparatus for improving the performance of a thermal breeder reactor having regions of higher than average moderator concentration are disclosed. The fuel modules of the reactor core contain at least two different types of fuel elements, a high enrichment fuel element and a low enrichment fuel element. The two types of fuel elements are arranged in the fuel module with the low enrichment fuel elements located between the high moderator regions and the high enrichment fuel elements. Preferably, shim rods made of a fertile material are provided in selective regions for controlling the reactivity of the reactor by movement of the shim rods into and out of the reactor core. The moderation of neutrons adjacent the high enrichment fuel elements is preferably minimized as by reducing the spacing of the high enrichment fuel elements and/or using a moderator having a reduced moderating effect.

Apollo 17 materials viewed from 2 to 4 mm soil particles: Pre-serenitatis highlands components

NASA Technical Reports Server (NTRS)

Jolliff, Bradley L.; Bishop, Kaylynn M.

1993-01-01

Among the highland lithologies of 2-4 mm rock fragments in North Massif soil 76503, we have found a compositional group, low in incompatible element concentrations, that we interpret as representing the pre-Serenitatis surface. A component of these materials is an igneous-textured lithology that we believe formed in large impact melts. These are compositionally similar to, and possibly precursors of, many of the granulitic breccias that appear to be mixtures of ferroan and magnesian-suite rocks. The polymict, or old, upper-crustal breccias, along with granulitic breccias and the endogenous igneous lithologies found particularly at the North Massif stations, constitute the poorly consolidated portions of North Massif. Highland samples from the South Massif, on the other hand, are enriched in materials of the competent, impact-melt breccias formed by the Serenitatis impact. The competent melt-breccias contain clasts of most of the pre-existing surface materials, but they also contain components not found in the rocks of the poorly consolidated massif materials.

Sulfide in the core and the Nd isotopic composition of the silicate Earth

NASA Astrophysics Data System (ADS)

McCoy-West, A.; Millet, M. A.; Nowell, G. M.; Wohlers, A.; Wood, B. J.; Burton, K. W.

2016-12-01

The chemical composition of the Earth is traditionally explained in terms of evolution from a solar-like composition, similar to that found in primitive chondritic meteorites. It now appears, however, that the silicate Earth is not chondritic, but depleted in incompatible elements and a resovable 20 ppm excess is observed in 142Nd relative to chondirtes [1, 2]. This anomaly requires a process that occurred within 30 Myr of solar system formation and has been variably ascribed to: a complementary enriched reservoir in the deep Earth [1]; loss to space through collisional erosion [3]; or the inhertence of nucleosynthetic anomalies [4]. Sulfide in the core may provide a reservoir capable of balancing the composition of the silicate Earth. Recent experimental work suggests that the core contains a significant proportion of sulfide, added during the final stages of accretion and new data suggests that at high pressures sulfide can incorporate a substantial amount of refractory lithophile and heat-producing elements [5]. The drawback of the short-lived 146Sm-142Nd radiogenic isotope system is that it is not possible to distinguish between fractionations of Sm/Nd that occurs during silicate melting or segregation of a sulfide-melt. Neodymium stable isotopes have the potential to provide just such a tracer of sulfide segregation, because there is a significant contrast in bonding environment between sulfide and silicate, where heavy isotopes should be preferentially incorporated into high force-constant bonds involving REE3+ (i.e. the silicate mantle). Preliminary data indicate that mantle rocks do indeed possess heavier 146Nd/144Nd values than chondritic meteorites by 0.3 ‰, consistent with the removal of light Nd into sulfide in the core, driving the residual mantle to heavier values. Overall, our isotope and elemental data indicate that the rare earths and other incompatible elements are substantially incorporated into sulfide. While Nd stable isotope data for chondritic meteorites and mantle rocks, are consistent with the segregation of sulfide to the core. [1] Boyet & Carlson, Science 309, 576 (2005) [2] Carlson et al. Science 316, 1175 (2007) [3] Campbell& O'Neill Nature 483, 553 (2012) [4] Burkhardt Goldschmidt Ab. 429 (2015) [5] Wohlers &Wood, Nature 520, 337 (2015)

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.

Petrographic and geochemical investigation of magma chamber processes beneath small Quaternary volcanic centers between Mt. Jefferson and Mt. Hood volcanoes, Cascade Range Volcanic Arc

NASA Astrophysics Data System (ADS)

Cunningham, E.; Cribb, J. W.

2017-12-01

The northern Oregon Cascade Range has been dominated by andesite to rhyodacite lavas at both Mt. Jefferson (Conrey, 1991) and at Mt. Hood (Cribb and Barton, 1996) during the Quaternary period. Eruptive sequences at both Mt. Hood and Mt. Jefferson have been attributed to open-system mama mixing (Kent et al., 2010) (Ferrell et al., 2015), and the narrow range of lavas erupted at both centers has been derived from repeated cycles of magma mixing-fractionation (Cribb and Barton, 1996). This research examines major and trace element geochemistry as well as the petrographic characteristics of Clear Lake Butte (CLB), Pinhead Butte (PB), and Olallie Butte (OB), all of which are located between Mt. Hood and Mt. Jefferson, and have ben active in the Quaternary period. The research investigates whether the same type of open-system magma mixing known to have occurred at Mt. Hood and Mt. Jefferson has also occurred at CLB, PB, or OB, or whether those systems were closed to mixing and dominated by fractional crystallization. One of the main goals of this project is to highlight the similarities and differences exhibited by neighboring magmatic systems of similar age, but different scale. Disequilibrium textures observed in thin sections from CLB, OB, and PB suggest open-system magma mixing is likely occurring beneath all three buttes. This petrographic evidence includes plagioclase and pyroxene zoning, embayed margins, sieving, and reaction rims. Major element oxide trends at all three buttes are consistent with fractional crystallization, but show narrow concentrations and non-overlapping compositions between PB, CLB, and OB. All three buttes are characterized by narrow ranges of incompatible and compatible trace element concentrations. CLB, PB, and OB all exhibit LREE enrichment and lack significant HFSE depletions, with PB exhibiting greatest enrichment in REE.

Geochemical Evidence Against Pyroxenites in the Sources of Hawaiian Volcanoes

NASA Astrophysics Data System (ADS)

Humayun, M.; Yang, S.; Clague, D. A.

2017-12-01

Hawaiian lavas exhibit high Fe/Mn ratios, and other elemental and isotopic characteristics, that have been argued to be evidence for chemical interactions at the core-mantle boundary. Alternatively, the enrichment in silica relative to 3 GPa melts of garnet peridotite, and the high Fe/Mn, has been argued to represent the contributions of garnet pyroxenite melts generated beneath a thick lithosphere. Here, we present a set of new elemental ratios designed to effectively discriminate partial melts of peridotite from pyroxenite in mantle sources. A set of 200 Hawaiian volcanic glasses from 7 volcanoes were analyzed by LA-ICP-MS for the abundances of 63 elements, with an emphasis on obtaining precise Ge/Si ratios. From experimental partitioning, silica-rich partial melts of MORB-like garnet pyroxenite are expected to have low Ge/Si ratios relative to their sources due to the retention of Ge in the residue by both garnet and pyroxene. In contrast, partial melts of peridotite are expected to have high Ge/Si ratios relative to mantle peridotites due to the incompatibility of Ge in olivine. We observed that Ge abundances in subaerial Hawaiian volcanoes are correlated with indicators of volcanic degassing, including S, Re and As. Subaerial and submarine lavas exhibit a correlation between Ge/Si ratio and S content that indicates that all Hawaiian lavas share the same pre-eruptive Ge/Si ratio. Submarine glasses with the least evidence of degassing exhibit a constant Ge/Si ratio over the range of SiO2 (44-52 %) observed in Hawaiian volcanics. Surprisingly, MORB glasses exhibit more variation in Ge/Si ratio than the pre-eruptive Ge/Si of Hawaiian glasses, implying the presence of 0-12% recycled crust in the MORB source. The constant Ge/Si ratio of Hawaiian glasses implies that pyroxenite melting did not enrich Hawaiian lavas in silica. Processes that could yield Si-rich melts without changing the Ge/Si ratio may involve melt-lithosphere interaction or bridgmanite/ferropericlase fractionation in the deep mantle.

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.

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.

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.

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

NASA Astrophysics Data System (ADS)

Ogawa, Masaki

2018-02-01

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

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.

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.

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.

Inclusions in diamonds constrain thermo-chemical conditions during Mesozoic metasomatism of the Kaapvaal cratonic mantle

NASA Astrophysics Data System (ADS)

Weiss, Yaakov; Navon, Oded; Goldstein, Steven L.; Harris, Jeff W.

2018-06-01

Fluid/melt inclusions in diamonds, which were encapsulated during a metasomatic event and over a short period of time, are isolated from their surrounding mantle, offering the opportunity to constrain changes in the sub-continental lithospheric mantle (SCLM) that occurred during individual thermo-chemical events, as well as the composition of the fluids involved and their sources. We have analyzed a suite of 8 microinclusion-bearing diamonds from the Group I De Beers Pool kimberlites, South Africa, using FTIR, EPMA and LA-ICP-MS. Seven of the diamonds trapped incompatible-element-enriched saline high density fluids (HDFs), carry peridotitic mineral microinclusions, and substitutional nitrogen almost exclusively in A-centers. This low-aggregation state of nitrogen indicates a short mantle residence times and/or low mantle ambient temperature for these diamonds. A short residence time is favored because, elevated thermal conditions prevailed in the South African lithosphere during and following the Karoo flood basalt volcanism at ∼180 Ma, thus the saline metasomatism must have occurred close to the time of kimberlite eruptions at ∼85 Ma. Another diamond encapsulated incompatible-element-enriched silicic HDFs and has 25% of its nitrogen content residing in B-centers, implying formation during an earlier and different metasomatic event that likely relates to the Karoo magmatism at ca. 180 Ma. Thermometry of mineral microinclusions in the diamonds carrying saline HDFs, based on Mg-Fe exchange between garnet-orthopyroxene (Opx)/clinopyroxene (Cpx)/olivine and the Opx-Cpx thermometer, yield temperatures between 875-1080 °C at 5 GPa. These temperatures overlap with conditions recorded by touching inclusion pairs in diamonds from the De Beers Pool kimberlites, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250 °C compared to P-T gradients recorded by peridotite xenoliths from the same locality. Oxygen fugacity (fO2) differs as well. The fO2 calculated for the saline HDF compositions (Δlog ⁡ fO 2 (FMQ) = - 2.47 to -1.34) are higher by about a log unit compared with that recorded by xenoliths at 4-7 GPa. We conclude that enriched saline HDFs mediated the metasomatism that preceded Group I kimberlite eruptions in the southwestern Kaapvaal craton, and that their 'cold and oxidized' nature reflects their derivation from a deep subducting slab. This event had little impact on the temperature and redox state of the Kaapvaal lithosphere as a reservoir, however, it likely affected its properties along limited metasomatized veins and their wall rock. To reconcile the temperature and oxygen fugacity discrepancy between inclusions in diamonds and xenoliths, we argue that xenoliths did not equilibrate during the last saline metasomatic event or kimberlite eruption. Thus the P-T- fO2 gradients they record express pre-existing lithospheric conditions that were likely established during the last major thermal event in the Kaapvaal craton (i.e. the Karoo magmatism at ca. 180 Ma).

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

NASA Astrophysics Data System (ADS)

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

2018-06-01

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

Geochemistry of serpentinites in subduction zones: A review

NASA Astrophysics Data System (ADS)

Deschamps, Fabien; Godard, Marguerite; Guillot, Stéphane; Hattori, Kéiko

2013-04-01

Over the last decades, numerous studies have emphasized the role of serpentinites in the subduction zones geodynamics. Their presence and effective role in this environment is acknowledged notably by geophysical, geochemical and field observations of (paleo-) subduction zones. In this context, with the increasing amount of studies concerning serpentinites in subduction environments, a huge geochemical database was created. Here, we present a review of the geochemistry of serpentinites, based on the compilation of ~ 900 geochemical analyses of abyssal, mantle wedge and subducted serpentinites. The aim was to better understand the geochemical evolution of these rocks during their subduction history as well as their impact in the global geochemical cycle. When studying serpentinites, it is often a challenge to determine the nature of the protolith and their geological history before serpentinisation. The present-day (increasing) geochemical database for serpentinites indicates little to no mobility of incompatible elements at the scale of the hand-sample in most serpentinized peridotites. Thus, Rare Earth Elements (REE) distribution can be used to identify the initial protolith for abyssal and mantle wedge serpentinites, as well as magmatic processes such as melt/rock interactions taking place before serpentinisation. In the case of subducted serpentinites, the interpretation of trace element data is more difficult due to secondary enrichments independent of the nature of the protolith, notably in (L)REE. We propose that these enrichments reflect complex interactions probably not related to serpentinisation itself, but mostly to fluid/rock or sediment/rock interactions within the subduction channel, as well as intrinsic feature of the mantle protolith which could derive from the continental lithosphere exhumed at the ocean-continent transition. Additionally, during the last ten years, numerous studies have been carried out, notably using in situ approaches, to better constrain the geochemical budget of fluid-mobile elements (FME; e.g. B, Li, Cl, As, Sb, U, Th, Sr) stored in serpentinites and serpentine phases. These elements are good markers of the fluid/rock interactions taking place during serpentinisation. Today, the control of serpentinites on the behaviour of these elements, from their incorporation to their gradually release during subduction, is better understood. Serpentinites must be considered as a component of the FME budget in subduction zones and their role, notably on arc magmas composition, is undoubtedly underestimated presently in the global geochemical cycle.

Volcanism on the fossil Galapagos Rise spreading centre, SE Pacific

NASA Astrophysics Data System (ADS)

Haase, K. M.; Stroncik, N. A.

2002-12-01

A part of the fossil spreading centre of the Galapagos Rise at 10° S, 95° W in the SE Pacific Ocean was mapped and sampled. This spreading centre was active for about 12 Ma and was abandoned about 6.5 Ma ago when the spreading rate of the East Pacific Rise (EPR) increased. The aim of this study is to understand the tectonic and petrological implications of the ridge jump for the spreading centre and to gain insights into the processes in its melting column. Bathymetric swath mapping of a part of the Galapagos Rise revealed an elongated structure with a NNE-SSW strike direction which is bounded by a large fracture zone in the north. The mapped area can be divided into three segments, each of about 50 km length. The northernmost segment consists of an ~4400 m deep rift which shows similarities to a slow-spreading centre, e.g. the Mid-Atlantic Ridge. The southern two segments are volcanic ridges with numerous volcanic flank cones which reach water depths up to 490 m. This volcanic ridge is interpreted as the continuation of the fossil spreading axis. While the northernmost segment is magmatically starved, the volcanic ridges of the southern two segments apparently formed after cessation of spreading. The rock samples from the rift flanks in the north are incompatible element-depleted (K/Ti 0.08-0.28) and plagioclase-phyric basalts resembling typical mid-ocean ridge basalts (MORB). In contrast, the lavas from the two volcanic ridge segments in the south are highly vesicular incompatible element-enriched alkali basalts with K/Ti of 0.65-1.4. The depleted rift basalts have Sr isotope ratios below 0.7027 while the alkali basalts from the ridge range between 0.7029 and 0.7031. The rift basalts have significantly lower sodium contents than the alkali basalts and thus the southern lavas are probably derived by smaller degrees of partial melting. The relatively low Si contents of the alkali basalts also indicates formation deeper in the melting column than the northern MORB-like samples. The mantle source of the alkali basalts is similar to the enriched source of off-axis seamounts along the EPR. Our preliminary data suggest that the northernmost segment formed by tectonic processes during a final slow-spreading phase of the Galapagos Rise while the southern two segments erupted alkaline lavas probably after spreading stopped.

Assisted suicide of a selfish gene.

PubMed

Thomson, M S; Beeman, R W

1999-01-01

Medea (M) factors and the hybrid incompatibility factor (H) are involved in two incompatibility systems in flour beetles that were previously thought to be independent. M factors are a novel class of selfish genes that act by maternal lethality to nonself. The H factor causes the death of hybrids with a paternally derived H gene and previously uncharacterized maternal cofactors. We now find that M factors exhibit their selfish behavior only in the absence of the H factor. Furthermore, we show that the previously uncharacterized maternal cofactors required for H-associated hybrid inviability are identical to M factors. We propose that incompatibility between H strains and M strains is due to suppression by the H factor of the self-rescuing activity of the lethal M genes. This interaction has the effect of converting M elements from selfish into self-destructive or "suicidal" genes. M factors are globally widespread, but are conspicuously absent from India, the only country where the H factor is known to occur. Such a mechanism could prevent the spread of selfish M elements by establishing an absolute barrier to hybridization in the boundary between M and non-M zones.

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.

Bulk Chemistry and Oxygen Isotopic Compositions of Lunar Meteorites Dhofar 025 and Dhofar 026

NASA Astrophysics Data System (ADS)

Taylor, L. A.; Nazarov, M. A.; Cohen, B. A.; Warren, P. H.; Barsukova, L. D.; Clayton, R. N.; Mayeda, T. K.

2001-03-01

The major- and trace-element composition of highlands meteorites Dh25 and Dh26 show that both are dominated by a FAN component. Incompatible element depletion and low Ti abundances suggest a farside origin. O-isotopes are typical for lunar meteorites.

Petrogenesis and origin of the Upper Jurassic-Lower Cretaceous magmatism in Central High Atlas (Morocco): Major, trace element and isotopic (Sr-Nd) constraints

NASA Astrophysics Data System (ADS)

Essaifi, Abderrahim; Zayane, Rachid

2018-01-01

During an uplift phase, which lasted ca. 40 Ma, from the Late Jurassic (165 Ma) to the Early Cretaceous (125 Ma), transitional to moderately alkaline magmatic series were emplaced in the Central High Atlas. The corresponding magmatic products include basaltic lava flows erupted within wide synclines and intrusive complexes composed of layered mafic intrusions and monzonitic to syenitic dykes emplaced along narrow anticlinal ridges. The igneous rock sequence within the intrusive complexes is composed of troctolites, olivine-gabbros, oxide-gabbros, monzonites and syenites. The chemical compositions of the various intrusive rocks can be accounted for by crystal accumulation, fractional crystallization and post-magmatic remobilization. The evolution from the troctolites to the syenites was mainly controlled by a fractional crystallization process marked by early fractionation of olivine, plagioclase and clinopyroxene, followed by separation of biotite, amphibole, apatite, and Ti-magnetite. Hydrothermal activity associated with emplacement of the intrusions within the Jurassic limestones modified the elemental and the Sr isotopic composition of the hydrothermally altered rocks In particular the monzonitic to syenitic dykes underwent an alkali metasomatism marked by depletion in K and Rb and enrichment in Na and Sr. As a result, their Sr isotopic composition was shifted towards higher initial Sr isotopic ratios (0.7067-0.7075) with respect to the associated gabbros (0.7036-0.7046). On the contrary, the Nd isotopic compositions were preserved from isotope exchange with the limestones and vary in a similar range to those of the gabbros (+1.6 < εNdi < +4.1). The isotopic and the trace element ratios of the uncontaminated samples were used to constrain the source characteristics of this magmatism. The Sr-Nd isotopic data and the incompatible element ratios (e.g. La/Nb, Zr/Nb, Th/U, Ce/Pb) are consistent with generation from an enriched upper mantle similar to an ocean island basalt source. Melting of the subcontinental metasomatized lithosphere is tentatively related to small-scale shallow mantle upwelling and asthenospheric uprise at the triple junction between the western High Atlas, the Middle Atlas and the eastern High Atlas domains during a period of relative tectonic quiescence.

The cosmological density of baryons from observations of 3He+ in the Milky Way.

PubMed

Bania, T M; Rood, Robert T; Balser, Dana S

2002-01-03

Primordial nucleosynthesis after the Big Bang can be constrained by the abundances of the light elements and isotopes 2H, 3He, 4He and 7Li (ref. 1). The standard theory of stellar evolution predicts that 3He is also produced by solar-type stars, so its abundance is of interest not only for cosmology, but also for understanding stellar evolution and the chemical evolution of the Galaxy. The 3He abundance in star-forming (H II) regions agrees with the present value for the local interstellar medium, but seems to be incompatible with the stellar production rates inferred from observations of planetary nebulae, which provide a direct test of stellar evolution theory. Here we develop our earlier observations, which, when combined with recent theoretical developments in our understanding of light-element synthesis and destruction in stars, allow us to determine an upper limit for the primordial abundance of 3He relative to hydrogen: 3He/H = (1.1 +/- 0.2) x 10(-5). The primordial density of all baryons determined from the 3He data is in excellent agreement with the densities calculated from other cosmological probes. The previous conflict is resolved because most solar-mass stars do not produce enough 3He to enrich the interstellar medium significantly.

Archaean ultra-depleted komatiites formed by hydrous melting of cratonic mantle.

PubMed

Wilson, A H; Shirey, S B; Carlson, R W

2003-06-19

Komatiites are ultramafic volcanic rocks containing more than 18 per cent MgO (ref. 1) that erupted mainly in the Archaean era (more than 2.5 gigayears ago). Although such compositions occur in later periods of Earth history (for example, the Cretaceous komatiites of Gorgona Island), the more recent examples tend to have lower MgO content than their Archaean equivalents. Komatiites are also characterized by their low incompatible-element content, which is most consistent with their generation by high degrees of partial melting (30-50 per cent). Current models for komatiite genesis include the melting of rock at great depth in plumes of hot, diapirically rising mantle or the melting of relatively shallow mantle rocks at less extreme, but still high, temperatures caused by fluxing with water. Here we report a suite of ultramafic lava flows from the Commondale greenstone belt, in the southern part of the Kaapvaal Craton, which represents a previously unrecognized type of komatiite with exceptionally high forsterite content of its igneous olivines, low TiO(2)/Al(2)O(3) ratio, high silica content, extreme depletion in rare-earth elements and low Re/Os ratio. We suggest a model for their formation in which a garnet-enriched residue left by earlier cratonic volcanism was melted by hydration from a subducting slab.

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.

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.

Glass in the submarine section of the HSDP2 drill core, Hilo, Hawaii

NASA Astrophysics Data System (ADS)

Stolper, Edward; Sherman, Sarah; Garcia, Michael; Baker, Michael; Seaman, Caroline

2004-07-01

The Hawaii Scientific Drilling Project recovered ˜3 km of basalt by coring into the flank of Mauna Kea volcano at Hilo, Hawaii. Rocks recovered from deeper than ˜1 km were deposited below sea level and contain considerable fresh glass. We report electron microprobe analyses of 531 glasses from the submarine section of the core, providing a high-resolution record of petrogenesis over ca. 200 Kyr of shield building of a Hawaiian volcano. Nearly all the submarine glasses are tholeiitic. SiO2 contents span a significant range but are bimodally distributed, leading to the identification of low-SiO2 and high-SiO2 magma series that encompass most samples. The two groups are also generally distinguishable using other major and minor elements and certain isotopic and incompatible trace element ratios. On the basis of distributions of high- and low-SiO2 glasses, the submarine section of the core is divided into four zones. In zone 1 (1079-˜1950 mbsl), most samples are degassed high-SiO2 hyaloclastites and massive lavas, but there are narrow intervals of low-SiO2 hyaloclastites. Zone 2 (˜1950-2233 mbsl), a zone of degassed pillows and hyaloclastites, displays a continuous decrease in silica content from bottom to top. In zone 3 (2233-2481 mbsl), nearly all samples are undegassed low-SiO2 pillows. In zone 4 (2481-3098 mbsl), samples are mostly high-SiO2 undegassed pillows and degassed hyaloclastites. This zone also contains most of the intrusive units in the core, all of which are undegassed and most of which are low-SiO2. Phase equilibrium data suggest that parental magmas of the low-SiO2 suite could be produced by partial melting of fertile peridotite at 30-40 kbar. Although the high-SiO2 parents could have equilibrated with harzburgite at 15-20 kbar, they could have been produced neither simply by higher degrees of melting of the sources of the low-SiO2 parents nor by mixing of known dacitic melts of pyroxenite/eclogite with the low-SiO2 parents. Our hypothesis for the relationship between these magma types is that as the low-SiO2 magmas ascended from their sources, they interacted chemically and thermally with overlying peridotites, resulting in dissolution of orthopyroxene and clinopyroxene and precipitation of olivine, thereby generating high-SiO2 magmas. There are glasses with CaO, Al2O3, and SiO2 contents slightly elevated relative to most low-SiO2 samples; we suggest that these differences reflect involvement of pyroxene-rich lithologies in the petrogenesis of the CaO-Al2O3-enriched glasses. There is also a small group of low-SiO2 glasses distinguished by elevated K2O and CaO contents; the sources of these samples may have been enriched in slab-derived fluid/melts. Low-SiO2 glasses from the top of zone 3 (2233-2280 mbsl) are more alkaline, more fractionated, and incompatible-element-enriched relative to other glasses from zone 3. This excursion at the top of zone 3, which is abruptly overlain by more silica-rich tholeiitic magmas, is reminiscent of the end of Mauna Kea shield building higher in the core.

Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants.

PubMed

Markunas, Christina A; Johnson, Eric O; Hancock, Dana B

2017-07-01

Genome-wide association study (GWAS)-identified variants are enriched for functional elements. However, we have limited knowledge of how functional enrichment may differ by disease/trait and tissue type. We tested a broad set of eight functional elements for enrichment among GWAS-identified SNPs (p < 5×10 -8 ) from the NHGRI-EBI Catalog across seven disease/trait categories: cancer, cardiovascular disease, diabetes, autoimmune disease, psychiatric disease, neurological disease, and anthropometric traits. SNPs were annotated using HaploReg for the eight functional elements across any tissue: DNase sites, expression quantitative trait loci (eQTL), sequence conservation, enhancers, promoters, missense variants, sequence motifs, and protein binding sites. In addition, tissue-specific annotations were considered for brain vs. blood. Disease/trait SNPs were compared to a control set of 4809 SNPs matched to the GWAS SNPs (N = 1639) on allele frequency, gene density, distance to nearest gene, and linkage disequilibrium at ~3:1 ratio. Enrichment analyses were conducted using logistic regression, with Bonferroni correction. Overall, a significant enrichment was observed for all functional elements, except sequence motifs. Missense SNPs showed the strongest magnitude of enrichment. eQTLs were the only functional element significantly enriched across all diseases/traits. Magnitudes of enrichment were generally similar across diseases/traits, where enrichment was statistically significant. Blood vs. brain tissue effects on enrichment were dependent on disease/trait and functional element (e.g., cardiovascular disease: eQTLs P TissueDifference  = 1.28 × 10 -6 vs. enhancers P TissueDifference  = 0.94). Identifying disease/trait-relevant functional elements and tissue types could provide new insight into the underlying biology, by guiding a priori GWAS analyses (e.g., brain enhancer elements for psychiatric disease) or facilitating post hoc interpretation.

Copahue volcano and its regional magmatic setting

USGS Publications Warehouse

Varekamp, J C; Zareski, J E; Camfield, L M; Todd, Erin

2016-01-01

Copahue volcano (Province of Neuquen, Argentina) has produced lavas and strombolian deposits over several 100,000s of years, building a rounded volcano with a 3 km elevation. The products are mainly basaltic andesites, with the 2000–2012 eruptive products the most mafic. The geochemistry of Copahue products is compared with those of the main Andes arc (Llaima, Callaqui, Tolhuaca), the older Caviahue volcano directly east of Copahue, and the back arc volcanics of the Loncopue graben. The Caviahue rocks resemble the main Andes arc suite, whereas the Copahue rocks are characterized by lower Fe and Ti contents and higher incompatible element concentrations. The rocks have negative Nb-Ta anomalies, modest enrichments in radiogenic Sr and Pb isotope ratios and slightly depleted Nd isotope ratios. The combined trace element and isotopic data indicate that Copahue magmas formed in a relatively dry mantle environment, with melting of a subducted sediment residue. The back arc basalts show a wide variation in isotopic composition, have similar water contents as the Copahue magmas and show evidence for a subducted sedimentary component in their source regions. The low 206Pb/204Pb of some backarc lava flows suggests the presence of a second endmember with an EM1 flavor in its source. The overall magma genesis is explained within the context of a subducted slab with sediment that gradually looses water, water-mobile elements, and then switches to sediment melt extracts deeper down in the subduction zone. With the change in element extraction mechanism with depth comes a depletion and fractionation of the subducted complex that is reflected in the isotope and trace element signatures of the products from the main arc to Copahue to the back arc basalts.

Volume gain during shearing of the Whatley Mill Gneiss, Pine Mountain Basement massif, eastern Alabama--A trace element approach

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

Salpas, P.A.; Daniell, N.

1993-03-01

The Whatley Mill Gneiss is the most voluminous exposure of the Pine Mountain Basement massif in eastern Alabama. Its type lithology is a proto-mylonitic gneiss composed of K-spar augen, up to 5 cm in diameter, in a finer matrix of biotite, microcline, and quartz. Granulite-facies mineral assemblages in the Whatley Mill Gneiss have been completely retrograded to amphibolite- and greenschist-facies assemblages in response to deformation that produced shear zones paralleling the foliation of the gneiss. The augen gneiss and its associated mylonites are well-exposed in a creek bed in Chewacla State Park. At this location the mineralogy of the mylonitesmore » is dominated by quartz indicating that shearing was associated with influx of a silica-rich fluid. A detailed geochemical study of these rocks shows that the augen gneiss displays relatively little variation in its major and trace element compositions while the quartz-rich mylonites display wider ranges, are enriched in SiO[sub 2] and depleted in the REE and other incompatible trace elements relative to the augen gneiss. When standard composition/volume calculations are applied to the mylonites the results show (1) the bulk of all of the elements, including the REE, were immobile during shearing with the exceptions of Si and Al which were added; and, (2) volume changes calculated using the REE as immobile elements range from +70% to +350%. Though these volume changes seem excessive, they apply to meter-thick shear zones which may actually represent only a small fraction of the total volume of the augen gneiss. Consistent with previous interpretations of these shear zones, the calculated volume gains imply shearing during extension.« less

Late-stage magmatic outgassing from a volatile-depleted Moon

PubMed Central

Moynier, Frédéric; Shearer, Charles K.

2017-01-01

The abundance of volatile elements and compounds, such as zinc, potassium, chlorine, and water, provide key evidence for how Earth and the Moon formed and evolved. Currently, evidence exists for a Moon depleted in volatile elements, as well as reservoirs within the Moon with volatile abundances like Earth’s depleted upper mantle. Volatile depletion is consistent with catastrophic formation, such as a giant impact, whereas a Moon with Earth-like volatile abundances suggests preservation of these volatiles, or addition through late accretion. We show, using the “Rusty Rock” impact melt breccia, 66095, that volatile enrichment on the lunar surface occurred through vapor condensation. Isotopically light Zn (δ66Zn = −13.7‰), heavy Cl (δ37Cl = +15‰), and high U/Pb supports the origin of condensates from a volatile-poor internal source formed during thermomagmatic evolution of the Moon, with long-term depletion in incompatible Cl and Pb, and lesser depletion of more-compatible Zn. Leaching experiments on mare basalt 14053 demonstrate that isotopically light Zn condensates also occur on some mare basalts after their crystallization, confirming a volatile-depleted lunar interior source with homogeneous δ66Zn ≈ +1.4‰. Our results show that much of the lunar interior must be significantly depleted in volatile elements and compounds and that volatile-rich rocks on the lunar surface formed through vapor condensation. Volatiles detected by remote sensing on the surface of the Moon likely have a partially condensate origin from its interior. PMID:28827322

Late-stage magmatic outgassing from a volatile-depleted Moon.

PubMed

Day, James M D; Moynier, Frédéric; Shearer, Charles K

2017-09-05

The abundance of volatile elements and compounds, such as zinc, potassium, chlorine, and water, provide key evidence for how Earth and the Moon formed and evolved. Currently, evidence exists for a Moon depleted in volatile elements, as well as reservoirs within the Moon with volatile abundances like Earth's depleted upper mantle. Volatile depletion is consistent with catastrophic formation, such as a giant impact, whereas a Moon with Earth-like volatile abundances suggests preservation of these volatiles, or addition through late accretion. We show, using the "Rusty Rock" impact melt breccia, 66095, that volatile enrichment on the lunar surface occurred through vapor condensation. Isotopically light Zn (δ 66 Zn = -13.7‰), heavy Cl (δ 37 Cl = +15‰), and high U/Pb supports the origin of condensates from a volatile-poor internal source formed during thermomagmatic evolution of the Moon, with long-term depletion in incompatible Cl and Pb, and lesser depletion of more-compatible Zn. Leaching experiments on mare basalt 14053 demonstrate that isotopically light Zn condensates also occur on some mare basalts after their crystallization, confirming a volatile-depleted lunar interior source with homogeneous δ 66 Zn ≈ +1.4‰. Our results show that much of the lunar interior must be significantly depleted in volatile elements and compounds and that volatile-rich rocks on the lunar surface formed through vapor condensation. Volatiles detected by remote sensing on the surface of the Moon likely have a partially condensate origin from its interior.

Late-stage magmatic outgassing from a volatile-depleted Moon

NASA Astrophysics Data System (ADS)

Day, James M. D.; Moynier, Frédéric; Shearer, Charles K.

2017-09-01

The abundance of volatile elements and compounds, such as zinc, potassium, chlorine, and water, provide key evidence for how Earth and the Moon formed and evolved. Currently, evidence exists for a Moon depleted in volatile elements, as well as reservoirs within the Moon with volatile abundances like Earth’s depleted upper mantle. Volatile depletion is consistent with catastrophic formation, such as a giant impact, whereas a Moon with Earth-like volatile abundances suggests preservation of these volatiles, or addition through late accretion. We show, using the “Rusty Rock” impact melt breccia, 66095, that volatile enrichment on the lunar surface occurred through vapor condensation. Isotopically light Zn (δ66Zn = -13.7‰), heavy Cl (δ37Cl = +15‰), and high U/Pb supports the origin of condensates from a volatile-poor internal source formed during thermomagmatic evolution of the Moon, with long-term depletion in incompatible Cl and Pb, and lesser depletion of more-compatible Zn. Leaching experiments on mare basalt 14053 demonstrate that isotopically light Zn condensates also occur on some mare basalts after their crystallization, confirming a volatile-depleted lunar interior source with homogeneous δ66Zn ≈ +1.4‰. Our results show that much of the lunar interior must be significantly depleted in volatile elements and compounds and that volatile-rich rocks on the lunar surface formed through vapor condensation. Volatiles detected by remote sensing on the surface of the Moon likely have a partially condensate origin from its interior.

Volatiles in basaltic glasses from a subglacial volcano in northern British Columbia (Canada): Implications for ice sheet thickness and mantle volatiles

USGS Publications Warehouse

Dixon, J.E.; Filiberto, J.R.; Moore, J.G.; Hickson, C.J.

2002-01-01

Dissolved H2O, CO2, S and Cl concentrations were measured in glasses from Tanzilla Mountain, a 500 m-high, exposed subglacial volcano from the Tuya-Teslin region, north central British Columbia, Canada. The absence of a flat-topped subaerial lava cap and the dominance of pillows and pillow breccias imply that the Tanzilla Mountain volcanic edifice did not reach a subaerial eruptive phase. Lavas are dominantly tholeiitic basalt with minor amounts of alkalic basalt erupted at the summit and near the base. Tholeiites have roughly constant H2O (c.0.56 ?? 0.07 wt%), CO2 (<30 ppm), S (980 ?? 30 ppm) and Cl (200 ?? 20 ppm) concentrations. Alkalic basalts have higher and more variable volatile concentrations that decrease with increasing elevation (0.62-0.92 wt% H2O, <30 ppm CO2, 870-1110 ppm S and 280-410 ppm Cl) consistent with eruptive degassing. Calculated vapour saturation pressures for the alkalic basalts are 36 to 81 bars corresponding to ice thicknesses of 400 to 900 m. Maximum calculated ice thickness (c. 1 km) is at the lower end of the range of predicted maximum Fraser glaciation (c. 1-2 km), and may indicate initiation of volcanism during the waning stages of glaciation. Temporal evolution from tholeiitic to alkalic compositions may reflect compositional gradients within a melting column, instead of convective processes within a stratified magma chamber. The mantle source region for the subglacial volcanoes is enriched in incompatible elements similar to that for enriched mid-oceanic ridge basalt (e.g. Endeavour Ridge) and does not contain residual amphibole. Thus, metasomatic enrichment most likely reflects small degree partial melts rather than hydrous fluids.

Formation of thick stratiform Fe-Ti oxide layers in layered intrusion and frequent replenishment of fractionated mafic magma: Evidence from the Panzhihua intrusion, SW China

NASA Astrophysics Data System (ADS)

Song, Xie-Yan; Qi, Hua-Wen; Hu, Rui-Zhong; Chen, Lie-Meng; Yu, Song-Yue; Zhang, Jia-Fei

2013-03-01

Panzhihua intrusion is one of the largest layered intrusions that hosts huge stratiform Fe-Ti oxide layers in the central part of the Emeishan large igneous province, SW China. Up to 60 m thick stratiform massive Fe-Ti oxide layers containing 85 modal% of magnetite and ilmenite and overlying magnetite gabbro compose cyclic units of the Lower Zone of the intrusion. The cyclic units of the Middle Zone consist of magnetite gabbro and overlying gabbro. In these cyclic units, contents of Fe2O3(t), TiO2 and Cr and Fe3+/Ti4+ ratio of the rocks decrease upward, Cr content of magnetite and forsterite percentage of olivine decrease as well. The Upper Zone consists of apatite gabbro characterized by enrichment of incompatible elements (e.g., 12-18 ppm La, 20-28 ppm Y) and increasing of Fe3+/Ti4+ ratio (from 1.3 to 2.3) upward. These features indicate that the Panzhihua intrusion was repeatedly recharged by more primitive magma and evolved magmas had been extracted. Calculations using MELTS indicate that extensive fractionation of olivine and clinopyroxene in deep level resulted in increasing Fe and Ti contents in the magma. When these Fe-Ti-enriched magmas were emplaced along the base of the Panzhihua intrusion, Fe-Ti oxides became an early crystallization phase, leading to a residual magma of lower density. We propose that the unusually thick stratiform Fe-Ti oxide layers resulted from coupling of gravity settling and sorting of the crystallized Fe-Ti oxides from Fe-Ti-enriched magmas and frequent magma replenishment along the floor of the magma chamber.

Subduction zone mantle enrichment by fluids and Zr-Hf-depleted crustal melts as indicated by backarc basalts of the Southern Volcanic Zone, Argentina

NASA Astrophysics Data System (ADS)

Holm, Paul M.; Søager, Nina; Alfastsen, Mads; Bertotto, Gustavo W.

2016-10-01

We aim to identify the components metasomatizing the mantle above the subducting Nazca plate under part of the Andean Southern Volcanic Zone (SVZ). We present new major and ICP-MS trace element and Sr, Nd and high-precision Pb isotope analyses of primitive olivine-phyric alkali basalts from the Northern Segment Volcanic Field, part of the Payenia province in the backarc of the Transitional SVZ. One new 40Ar-39Ar age determination confirms the Late Pleistocene age of this most northerly part of the province. All analysed rocks have typical subduction zone type incompatible element enrichment, and the rocks of the Northern Segment, together with the neighbouring Nevado Volcanic Field, have isotopic compositions intermediate between adjacent Transitional SVZ arc rocks and southern Payenia OIB-type basaltic rocks. Modelling the Ba-Th-Sm variation we demonstrate that fluids as well as 1-2% melts of upper continental crust (UCC) enriched their mantle sources, and La-Nb-Sm variations additionally indicate that the pre-metasomatic sources ranged from strongly depleted to undepleted mantle. Low Eu/Eu* and Sr/Nd also show evidence for a UCC component in the source. The contribution of Chile Trench sediments to the magmas seems insignificant. The Zr/Sm and Hf/Sm ratios are relatively low in many of the Northern Segment rocks, ranging down to 17 and 0.45, respectively, which, together with relatively high Th/U, is argued to indicate that the metasomatizing crustal melts were derived by partial melting of subducted UCC that had residual zircon, in contrast to the UCC melts added to Transitional SVZ arc magmas. Mixing between depleted and undepleted mantle, enriched by UCC and fluids, is suggested by Sr, Nd and Pb isotopes of the Northern Segment and Nevado magmas. The metasomatized undepleted mantle south of the Northern Segment is suggested to be part of upwelling OIB-type mantle, whereas the pre-metasomatically depleted mantle also can be found as a component in some arc rocks. The fluid-borne enrichment seems to have been derived from South Atlantic wedge mantle with no significant transfer of solubles in the slab fluids from the subducting altered Pacific oceanic crust to the wedge. The Northern Segment magmatism is proposed to be related to the steepening of Nazca plate subduction in the Pleistocene after a shallow slab period, where melts of subducted UCC plus slab fluids metasomatized the overlying depleted wedge mantle. During this steepening, the enriched depleted and undepleted mantle mixed or interacted, and yielded the Northern Segment and Nevado magmas.

Impact of Enteral Nutrition with an Immunomodulating Diet Enriched with Hydrolyzed Whey Peptide on Infection After Liver Transplantation.

PubMed

Kamo, Naoko; Kaido, Toshimi; Hamaguchi, Yuhei; Uozumi, Ryuji; Okumura, Shinya; Kobayashi, Atsushi; Shirai, Hisaya; Yagi, Shintaro; Okajima, Hideaki; Uemoto, Shinji

2018-05-21

Infection is a leading cause of death after liver transplantation (LT). Therefore, prevention of infection is crucial for improving outcomes after LT. We examined the impact of early enteral nutrition with an immunomodulating diet (IMD) enriched with hydrolyzed whey peptide (HWP) formulation on infection after living donor LT (LDLT), focusing on sarcopenia. This study enrolled 279 consecutive patients who underwent primary LDLT at our institute between January 2008 and April 2015. Early enteral nutrition with the IMD enriched with HWP formulation and a conventional elemental diet were started within the first 24 h after surgery for 164 (IMD-HWP) and 115 (conventional) patients. Sequential changes in nutritional parameters, and the incidences of acute cellular rejection (ACR) and bacteremia were compared between the IMD-HWP and control groups. The comparison was made between those members of each group that did or did not exhibit sarcopenia. Risk factors for post-transplant bacteremia were also assessed. Postoperative nutritional parameters and the incidence of ACR were comparable between the groups, except for the prealbumin level. The incidence of bacteremia was significantly lower in the IMD-HWP group, and among patients without sarcopenia in the IMD-HWP group compared with the conventional group (24.4 vs. 41.7%; P = 0.002 and 20.8 vs. 39.0%; P = 0.040, respectively). Independent risk factor for bacteremia comprised bleeding ≥10,000 mL (P = 0.025). In contrast, enteral nutrition without HWP formulation was not significantly associated with bacteremia. However, enteral nutrition without HWP formulation (P = 0.080), MELD scores (P = 0.097), and ABO incompatibility (P = 0.088) showed a trend toward increased incidence of bacteremia, although they did not reach statistical significance in the multivariate analysis. Postoperative immunonutrition with an IMD enriched with HWP formulation was closely involved with post-transplant bacteremia.

New Results for the Multi-stage Geochemical Evolution of the Manihiki and Hikurangi Plateaus (Invited)

NASA Astrophysics Data System (ADS)

Hoernle, K.; Timm, C.; Hauff, S. F.; Rupke, L.; Werner, R.; van den Bogaard, P.; Michael, P. J.; Coffin, M.; Mortimer, N. N.; Davy, B. W.

2009-12-01

The Hikurangi and Manihiki Plateaus, extensively sampled on the SONNE 168 and 193 cruises, have a similar temporal and geochemical evolution. The two plateaus began with a main tholeiitic plateau stage (c. 126-116 Ma) followed by a later (seamount-forming) alkalic stage of volcanism (lasting more than 30 Ma on each plateau). The tholeiitic lavas have largely similar compositions to the Kwaimbaita/Kroenke and Singgalo lavas from the Ontong Java Plateau (OJP), but some from the Suvarov Trough on the Manihiki Plateau have distinct compositions similar to those reported by Ingle et al. (2007, Geology). Glasses from the tholeiitic plateau stage lavas from two different sites on the Manihiki Plateau have CO2 and H2O contents indicating depths of eruption of 900± 200 m and 1300 ± 200 m. The H2O/Ce ratios (220-400) are at the high end of MORB, similar to the OJP, and therefore volatiles are unlikely to play a major role in melt generation. Using the method of Herzberg and Asimov (2008, G3), the Manihiki tholeiites can be generated by ~30% melting of a peridotitic source at temperatures of ~1510°C (similar to results from the OJP). The S contents are even lower than for the OJP, suggesting that the source was depleted in S. The tholeiitic plateau stage lavas are characterized by generally flat incompatible element patterns on multi-element diagrams, similar to other oceanic plateaus such as the OJP. The mafic alkalic late stage lavas, on the other hand, have steep patterns (characteristic of ocean island basalts), indicating lower degrees of melting and/or enrichment in highly to moderately incompatible elements and residual garnet in the source relative to the plateau stage. The Sr-Nd-Pb-Hf isotope data for the plateau rocks indicate compositions ranging from E-MORB (or FOZO)-like, similar to the major Kwaimbaita/Kroenke compositional group of lavas on the OJP, to EM1-type compositions, characteristic of the Singgalo endmember on the OJP. The late-stage alkalic rocks range from E-MORB (FOZO) - like to HIMU-type isotopic compositions (with 206Pb/204Pb approaching 21) and are similar in composition to rare 90 Ma old alkalic dikes on the OJP. The geochemical data support a common origin and geochemical evolution for the Manihiki, Hikurangi and OJ plateaus. Evidence for large degrees of melting of an enriched peridotitic source at elevated mantle potential temperature favors a plume-type model for the origin of these plateau fragments. The late alkalic stage of volcanism, however, is more difficult to explain, since the plateaus were located thousands of kilometers apart when this volcanism primarily occurred (c. 70-100 Ma ago). We are exploring detachment/delamination and pulsating super-plume models to explain the origin of the late-stage volcanism.

Micron-Scale Correlations Among Ti, P, Ce, and Y in Hadean Jack Hills Zircons

NASA Astrophysics Data System (ADS)

Hofmann, A. E.; Cavosie, A. J.; Valley, J. W.; Eiler, J. M.

2007-12-01

Detrital zircons and the inclusions found therein are our only mineralogical constraints on geologic events that occurred on the Hadean Earth. These zircons are commonly small (ca. <100 μm in the longest dimension) and preserve micron to sub-micron chemical zonations indicative of a dynamic petrological history. Trace elements within zircon are of particular interest because concentrations and ratios of these elements can provide information regarding chemical and physical conditions during zircon growth. In this study, we analyzed Hadean-age detrital zircons from Archean metasediment in the Jack Hills (Australia) using the Caltech Microanalysis Center Cameca NanoSIMS 50L. Trace elements analyzed included Ti, P, Ce, and Y. Ti- thermometry [1,2,3] can potentially constrain growth and/or re-equilibration temperatures of zircons; P, Ce, and Y are known to enter the zircon lattice by the coupled xenotime-type substitution mechanism: (Y, REE)3+ + P5+ = Zr4+ + Si4+ [5]. The 89Y/28Si ratio was observed to correlate with, and was used as a proxy for, cathodoluminescence (CL) banding. Growth features manifested in CL (e.g., sector, oscillatory zoning) were observed in all zircons analyzed. CL zones vary from <1 μm to several microns in width; therefore, the NanoSIMS---with a beam diameter resolved to ca. 250 nm on the sample surface when operating with an O- primary beam---is uniquely suited for this scale of analysis. Regions displaying CL banding were imaged as 20 x 20 μm areas. All elements were normalized to 28Si; 49Ti/28Si ratios were converted to [Ti] via calibration based on analyses of synthetic, high-Ti zircons (provided by B. Watson) that were independently analyzed on Caltech's JEOL JXA-8200 electron microprobe. We observe three types of relationships between trace element distribution and CL banding in the zircons imaged: 1) strong positive correlations between CL banding, P, Ce, and Ti; 2) subtle positive correlations between CL banding, P, Ce, and Ti; 3) no correlation between minor/trace elements and CL banding. Positive correlations between CL banding, 3+ cations, and [Ti] have previously been reported by Holden et al. [4]. In this study, gradients at least as sharp as a factor of ~3 in [Ti] are observed between adjacent CL bands in the strongly correlated images. These images also have the highest absolute concentrations of trace elements and display both sector and oscillatory zoning in CL. The correlations observed may be due to: temperature-dependent equilibrium partitioning of all trace elements during rapid cycles in growth temperature; episodic diffusion-limited enrichment of incompatible trace elements in the boundary layer melt adjacent to growing crystals; and/or kinetically controlled, non- equilibrium crystal-melt partitioning caused by trace element enrichments in the boundary layer melt surrounding fast-growing grains (e.g., [6]). We will discriminate between these alternatives based on quantitative relationships between relative enrichments of [Ti] and other trace elements. [1]Watson, E.B. & Harrison, T.M. (2005) Science 308, 841-844. [2]Watson, E.B., Wark, D.A., & Thomas, J.B. (2006) CMP 151, 413-433. [3]Ferry, J.M. & Watson, E.B. (2007) CMP 154, 429-437. [4] Holden, P. et al. (2005) Eos Trans. AGU 86 (52) Fall Meet. Suppl., Abstract V41F-1539. [5] Speer, J.A. (1982) Zircon. In Rev. Min. 5 (ed. P.H. Ribbe), 67-112. [6] Watson, E.B. (2004) GCA 68, 1473-1488.

A Strongly Calc-alkaline Suite in the Midst of the Tholeiitic Columbia River Basalt Province: Implications for Generating the Calc-alkaline Trend Without Subduction Processes

NASA Astrophysics Data System (ADS)

Steiner, A. R.; Streck, M. J.

2012-12-01

The mid-Miocene lavas of the Strawberry Volcanics (SV), distributed over 3,400 km2 in NE Oregon, comprise a diverse volcanic suite, which span the range of compositions from basalt to rhyolite. The volcanic suite is mainly composed of calc-alkaline (CA) basaltic andesite and andesite, yet tholeiitic (TH) lavas of basalt to andesite occur as well. The SV lies in the heart of nearly coeval flood basalts of the Columbia River province of the Pacific Northwest. The unique combination of strongly CA rocks of the SV in a non-subduction setting provide an excellent opportunity to study controls on inducing CA evolution in the midst of a TH province and independent of processes taking places at an active subduction zone. New 40Ar/39Ar ages indicate CA basaltic andesites to andesites of the SV erupted at least from 14.78±0.13 Ma to 12.44±0.12 Ma demonstrating that CA magmatism of the SV was ongoing during the eruptions of the tholeiitic Wanapum Basalt member of the Columbia River Basalt Group (CRBG). This range will likely be extended to even older ages in the future because existent age dates did not include samples from near the base of the SV. Thickness of intermediate lavas flows of the SV range from 15 m to as thin as 2 m and lavas are characterized by mostly phenocryst poor lithologies. When phenocrysts are abundant they are very small suggesting growth late during eruption. Single lava flow sections can include on the order of 30 conformable flows, testifying to a vigorous eruption history. The thickest andesitic sections are located in the glacially carved mountains of the Strawberry Mountain Wilderness (i.e. Strawberry Mountain, High Lake, and Slide Lake) where several vent complexes are exposed, which are delineated by dikes and plugs with finely interlocking plutonic textures, cross-cutting SV lava flows. Dikes generally strike NW-SE. Subtle variations in major and trace element compositions exist between TH and CA lavas of the SV. The CA lavas of the SV are more enriched in highly incompatible LIL while slightly more depleted in HFSE and REE, particularly HREE, relative to TH lavas. Incompatible trace elements range from the mafic to the silicic end as follows [in ppm]: Rb - CA: 11 to 43, TH: 4 to 37; Ba - CA: 550-1124, TH: 408 to 929; Th - CA: 1.2 to 4.0, TH: 1.2 to 3.5; Nb - CA: 6.0 to 16.2, TH: 9.3 to 23.1; Lu - CA: 0.3 to 0.49, TH: 0.3 to 0.63. On the other hand, great similarity among element patterns of CA and TH samples in incompatible element normalization diagrams is consistent with a common mafic component. Our preliminary interpretation is that CA magmas of the SV are generated when basaltic, CRBG-related magmas interact with the continental crust, while TH magmas escaped comparable crustal modifications. The range in compositions from basalt to CA andesite to dacite may thus be attributed to greater amounts of crustal inputs via magma mixing or AFC processes. Trace element concentrations and ratios of SV basalts are largely indistinguishable from those of CRBG lavas and have the greatest commonality with Steens and Imnaha type lavas (e.g. Zr, Ba, Sr, Th, U, Ba/Nb and Ce/Y).

Trace elements as quantitative probes of differentiation processes in planetary interiors

NASA Technical Reports Server (NTRS)

Drake, M. J.

1980-01-01

The characteristic trace element signature that each mineral in the source region imparts on the magma constitutes the conceptual basis for trace element modeling. It is shown that abundances of trace elements in extrusive igneous rocks may be used as petrological and geochemical probes of the source regions of the rocks if differentiation processes, partition coefficients, phase equilibria, and initial concentrations in the source region are known. Although compatible and incompatible trace elements are useful in modeling, the present review focuses primarily on examples involving the rare-earth elements.

An Enriched Shell Finite Element for Progressive Damage Simulation in Composite Laminates

NASA Technical Reports Server (NTRS)

McElroy, Mark W.

2016-01-01

A formulation is presented for an enriched shell nite element capable of progressive damage simulation in composite laminates. The element uses a discrete adaptive splitting approach for damage representation that allows for a straightforward model creation procedure based on an initially low delity mesh. The enriched element is veri ed for Mode I, Mode II, and mixed Mode I/II delamination simulation using numerical benchmark data. Experimental validation is performed using test data from a delamination-migration experiment. Good correlation was found between the enriched shell element model results and the numerical and experimental data sets. The work presented in this paper is meant to serve as a rst milestone in the enriched element's development with an ultimate goal of simulating three-dimensional progressive damage processes in multidirectional laminates.

Construction of Continental Crust at the Central American and Philippines Arc Systems

NASA Astrophysics Data System (ADS)

Whattam, S. A.; Stern, R. J.

2016-12-01

Whether or not magmatic arcs evolve compositionally with time and the processes responsible remain controversial. Resolution of this question requires reconstructing arc geochemical evolution at the level of discrete arc systems, as has been done for IBM, Central America, and the Greater Antilles. Emphasis should be on arcs built on oceanic crust because interaction with continental crust complicates interpretations. The Philippines are a particularly attractive target because this may be the best example where proto-continental crust has been generated and processed in Cretaceous and younger time. Here, we show how this question could be addressed for the Philippines using the well-studied Central American Volcanic Arc System (CAVAS) as an example. For the CAVAS, we avoided the northern arc segment because these are (Guatemala) or maybe (El Salvador) sections built on continental crust. Geochemical and isotopic data were compiled for 1031 samples of lavas and intrusive rocks from the 1100 km-long segment built on thickened, initially plume-derived oceanic crust over its 75 million year lifespan (Panama, Costa Rica, Nicaragua) . The most striking observation is the overall evolution of the CAVAS to more incompatible element enriched and ultimately continental-like compositions with time. Models entailing progressive arc magmatic enrichment are generally supported by the CAVAS record. Progressive enrichment of the oceanic CAVAS with time reflects changes in mantle wedge composition and decreased melting due to arc crust thickening, which was kick-started by the involvement of enriched plume mantle. Progressive crustal thickening and associated changes in the sub-arc thermal regime resulted in decreasing degrees of partial melting over time, which allowed for progressive enrichment of the CAVAS and ultimately the production of continental-like crust in Panama and Costa Rica by 16-10 Ma. Our similar study of the Philippine Arc system is in its infancy but earlier studies have shown that older magmatic rocks are tholeiitic and MORB-like whereas younger ones are invariably calc-alkaline and arc-like. Results of the Philippines Arc study will be compared with the CAVAS and other magmatic arc systems comprised of continental crust.

Mixing in heterogeneous internally-heated convection

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Pristine Igneous Rocks and the Early Differentiation of Planetary Materials

NASA Technical Reports Server (NTRS)

Warren, Paul H.

2005-01-01

Our studies are highly interdisciplinary, but are focused on the processes and products of early planetary and asteroidal differentiation, especially the genesis of the ancient lunar crust. The compositional diversity that we explore is the residue of process diversity, which has strong relevance for comparative planetology. Most of the accessible lunar crust consists of materials hybridized by impact-mixing. Our lunar research concentrates on the rare pristine (unmixed) samples that reflect the original genetic diversity of the early crust. Among HED basalts (eucrites and clasts in howardites), we distinguish as pristine the small minority that escaped the pervasive thermal metamorphism of the parent asteroid's crust. We have found a correlation between metamorphically pristine HED basalts and the similarly small minority of compositionally evolved "Stannern trend" samples, which are enriched in incompatible elements and titanium compared to main group eucrites, and yet have relatively high mg ratios. Other topics under investigation included: lunar and SNC (martian?) meteorites; igneous meteorites in general; impact breccias, especially metal-rich Apollo samples and polymict eucrites; siderophile compositions of the lunar and martian mantles; and planetary bulk compositions and origins.

Geochemical evolution of Kohala Volcano, Hawaii

USGS Publications Warehouse

Lanphere, M.A.; Frey, F.A.

1987-01-01

Kohala Volcano, the oldest of five shield volcanoes comprising the island of Hawaii, consists of a basalt shield dominated by tholeiitic basalt, Pololu Volcanics, overlain by alkalic lavas, Hawi Volcanics. In the upper Pololu Volcanics the lavas become more enriched in incompatible elements, and there is a transition from tholeiitic to alkalic basalt. In contrast, the Hawi volcanics consist of hawaiites, mugearites, and trachytes. 87Sr/86Sr ratios of 14 Pololu basalts and 5 Hawi lavas range from 0.70366 to 0.70392 and 0.70350 to 0.70355, respectively. This small but distinct difference in Sr isotopic composition of different lava types, especially the lower 87Sr/86Sr in the younger lavas with higher Rb/Sr, has been found at other Hawaiian volcanoes. Our data do not confirm previous data indicating Sr isotopic homogeneity among lavas from Kohala Volcano. Also some abundance trends, such as MgO-P2O5, are not consistent with a simple genetic relationship between Pololu and Hawi lavas. We conclude that all Kohala lavas were not produced by equilibrium partial melting of a compositionally homogeneous source. ?? 1987 Springer-Verlag.

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.

Hydrous parental magmas of Early to Middle Permian gabbroic intrusions in western Inner Mongolia, North China: New constraints on deep-Earth fluid cycling in the Central Asian Orogenic Belt

NASA Astrophysics Data System (ADS)

Pang, Chong-Jin; Wang, Xuan-Ce; Xu, Bei; Luo, Zhi-Wen; Liu, Yi-Zhi

2017-08-01

The role of fluids in the formation of the Permian-aged Xigedan and Mandula gabbroic intrusions in western Inner Mongolia was significant to the evolution of the Xing'an Mongolia Orogenic Belt (XMOB), and the active northern margin of the North China Craton (NCC). Secondary Ion Mass Spectroscopy (SIMS) U-Pb zircon geochronology establishes that the Xigedan gabbroic intrusion in the northern NCC was emplaced at 266 Ma, and is therefore slightly younger than the ca 280 Ma Mandula gabbroic intrusion in the XMOB. Along with their felsic counterparts, the mafic igneous intrusions record extensive bimodal magmatism along the northern NCC and in the XMOB during the Early to Middle Permian. The Mandula gabbroic rocks have low initial 87Sr/86Sr ratios (0.7040-0.7043) and positive εNd(t) (+6.2 to +7.3) and εHf(t) values (+13.4 to +14.5), resembling to those of contemporaneous Mandula basalts. These features, together with the presence of amphibole and the enrichment of large ion lithophile elements (LILE, e.g., Rb, Ba, U and Sr) and depletion of Nb-Ta suggest that the parental magmas of the Mandula mafic igneous rocks were derived from a depleted mantle source metasomatized by water-rich fluids. In contrast, the Xigedan gabbroic rocks are characterised by high 87Sr/86Sr ratios (0.7078-0.7080) and zircon δ18O values (5.84-6.61‰), but low εNd(t) (-9.3 to -10.2) and εHf(t) values (-8.76 to -8.54), indicative of a long-term enriched subcontinental lithosphere mantle source that was metasomatized by recycled, high δ18O crustal materials prior to partial melting. The high water contents (4.6-6.9 wt%) and arc-like geochemical signature (enrichment of fluid-mobile elements and depletion of Nb-Ta) of the parental magmas of the Xigedan gabbroic rocks further establish the existence of a mantle hydration event caused by fluid/melts released from hydrated recycled oceanic crust. Incompatible element modelling shows that 5-10% partial melting of an enriched mantle source by adding respectively 0.5% and 2% sediment melts and fluids, could have produced the parental magmas of the Xigedan gabbroic rocks. A range of geological evidence establishes an intracontinental origin for Late Paleozoic mafic igneous rocks along the northern NCC and in the XMOB, rather than a subduction-related setting. We therefore propose a deep-Earth water cycling process to account for mantle hydration and subsequent Late Paleozoic magmatism, supporting a geodynamic link between deep-Earth water cycling, and intracontinental magmatism and lithospheric extension.

Multiple reinjections and crystal mush compaction in the solidification evolution of the Karaj Dam basement Sill, Northern Iran

NASA Astrophysics Data System (ADS)

Maghdour-Mashhour, Reza; Shabani, Amir Ali Tabbakh

2017-07-01

The Karaj Dam basement Sill is a 460 m-thick saucer shaped sill, situated in the Alborz Magmatic Belt, Northern Iran. The results of geochemical, textural and field relations reveal characteristics of a sill with a well-developed S-shaped compositional profile which could be subdivided into distinct parts and suggest that the sill was repeatedly split and reinjected with fresh magma in the upper half of the previous emplacements (over- to partly intra-accretion). Whole rock and mineral compositional profiles have recorded five to six discrete injections of magma, each of which individually show an upward increase in terms of primitivity which represents partial crystallization in feeder conduits. The first three small successive pulses of magma, emplaced in the basal 150 m of the floor sequence, were followed by voluminous fourth and fifth pulses in the upper portion of the sill. During final two pulses the system acts as a closed system for each independently, and evolves through compositional convection or compaction aided in-situ crystallization. Theoretical models for convection and compaction shows the significance of both processes. Considering the final porosity of 0.1 < φ < 0.45, calculated convective velocities (0.2 < Vc < 227 m/year) are higher than the calculated crystal accumulation rate of the basal 150 m and upper portion of the sill (Va = 1 and 0.1 m/year), when the crystal mush varies between 1 to 0.01 m with the liquid viscosity ranging from 85 to 15 Pa·s. Our calculations further indicate that compaction driven velocity of liquid expulsion (ω - w) hardly exceeds the Va in the basal 150 m of the floor sequence. The highest velocity is reached (ω - w = 1 m/year) only if the crystal mush thickness is no less than 240 m with the porosity of 0.6 and the liquid viscosity of no more than 15 Pa·s. On the other hand, compaction is highly effective in the upper portion of the sill. Transfer of residual liquid from the compacting lower solidification front to the dilating upper solidification front resulted in characteristic chemical and mineralogical effects, such as the depletion of the lower half of the sill and the enrichment of the sandwich zone in incompatible elements and modal granophyre. Crystallization of the fourth pulse of magma produced a peak in incompatible clement concentrations at a sandwich horizon located at the 410 m level, where the floor and roof of the sill appeared to converge at this stage. Subsequent to the time of this enriched zone crystallizing, the fifth pulse of magma was emplaced near this level and inflated the chamber vertically for 200 m. Cumulus material containing interstitial melt and subsequent buoyancy driven upward transport of interstitial melt in this pulse concentrated incompatible elements at 47 m below the main peak, at the stratigraphic height of 360-370 m. The boundaries between the successive pulses were cryptic and represent a gradational contact in terms of grain size, chemical composition and crystallization sequence. This implies a short time interval between the emplacements of the magma. This sill is comparable with Antarctica Beacon Sill and Hudson River Palisades Sill, and the recognition of evidence for reinjection and compaction in these macroscopically uniform sills, as well as the Karaj Dam basement Sill, suggests that these processes may be common in the construction of sills with a thickness of more than 100 m.

Magma transport and metasomatism in the mantle: a critical review of current geochemical models

USGS Publications Warehouse

Nielson, J.E.; Wilshire, H.G.

1993-01-01

Conflicting geochemical models of metasomatic interactions between mantle peridotite and melt all assume that mantle reactions reflect chromatographic processes. Examination of field, petrological, and compositional data suggests that the hypothesis of chromatographic fractionation based on the supposition of large-scale percolative processes needs review and revision. Well-constrained rock and mineral data from xenoliths indicate that many elements that behave incompatibly in equilibrium crystallization processes are absorbed immediately when melts emerge from conduits into depleted peridotite. After reacting to equilibrium with the peridotite, melt that percolates away from the conduit is largely depleted of incompatible elements. Continued addition of melts extends the zone of equilibrium farther from the conduit. Such a process resembles ion-exchange chromatography for H2O purification, rather than the model of chromatographic species separation. -from Authors

Melt/mantle interaction and melt evolution in the Sartohay high-Al chromite deposits of the Dalabute ophiolite (NW China)

NASA Astrophysics Data System (ADS)

Zhou, M.-F.; Robinson, P. T.; Malpas, J.; Aitchison, J.; Sun, M.; Bai, W.-J.; Hu, X.-F.; Yang, J.-S.

2001-06-01

The Sartohay block of the Dalabute ophiolite consists chiefly of mantle harzburgite and lherzolite with minor dunite. These rocks host voluminous chromite deposits with lenticular or vein-like shapes. The podiform chromitites are associated with, and cross-cut by, numerous troctolite dykes. Chromite in the chromitites has Al 2O 3 (23-31 wt%), TiO 2 (0.29-0.44 wt%), and Cr 2O 3 contents (<45 wt%) with Cr#s [100Cr/(Cr+Al)] (<60), typical of high-Al chromite deposits. The host peridotites in Sartohay have been texturally and geochemically modified by magmas from which the high-Al chromitites and mafic dykes formed. Dunites commonly envelop the podiform chromite bodies and show transitional contacts with the peridotites. Some of the peridotites and chromitites contain plagioclase that crystallized from impregnated melts. The dunite locally grades into troctolite with increasing plagioclase contents. As a result of melt impregnation, peridotites and dunites show variable Ca and Al contents and LREE enrichment. The parental magma of the chromitites was likely tholeiitic in composition, derived from partial melting of the asthenospheric mantle in a rising diapir. The interaction between this magma and pre-existing lithospheric mantle, composed of depleted lherzolite, would have formed a more silicic, tholeiitic magma from which high-Al chromitites crystallized. During this interaction, harzburgite and dunite were depleted in modal pyroxene and enriched in some incompatible elements (such as Al, Ca and LREE) due to melt impregnation.

Petrogenesis and tectonic implications of Late Carboniferous A-type granites and gabbronorites in NW Iran: Geochronological and geochemical constraints

NASA Astrophysics Data System (ADS)

Moghadam, Hadi Shafaii; Li, Xian-Hua; Ling, Xiao-Xiao; Stern, Robert J.; Santos, Jose F.; Meinhold, Guido; Ghorbani, Ghasem; Shahabi, Shirin

2015-01-01

Carboniferous igneous rocks constitute volumetrically minor components of Iranian crust but preserve important information about the magmatic and tectonic history of SW Asia. Ghushchi granites and gabbronorites in NW Iran comprise a bimodal magmatic suite that intruded Ediacaran-Cambrian gneiss and are good representatives of carboniferous igneous activity. Precise SIMS U-Pb zircon ages indicate that the gabbronorites and granites were emplaced synchronously at ~ 320 Ma. Ghushchi granites show A-type magmatic affinities, with typical enrichments in alkalis, Ga, Zr, Nb and Y, depletion in Sr and P and fractionated REE patterns showing strong negative Eu anomalies. The gabbronorites are enriched in LREEs, Nb, Ta and other incompatible trace elements, and are similar in geochemistry to OIB-type rocks. Granites and gabbronorites have similar εNd(t) (+ 1.3 to + 3.4 and - 0.1 to + 4.4, respectively) and zircon εHf(t) (+ 1.7 to + 6.2 and + 0.94 to + 6.5, respectively). The similar variation in bulk rock εNd(t) and zircon εHf(t) values and radiometric ages for the granites and gabbronorites indicate a genetic relationship between mafic and felsic magmas, either a crystal fractionation or silicate liquid immiscibility process; further work is needed to resolve petrogenetic details. The compositional characteristics of the bimodal Ghushchi complex are most consistent with magmatic activity in an extensional tectonic environment. This extension may have occurred during rifting of Cadomian fragments away from northern Gondwana during early phases of Neotethys opening.

Incompatibility and competitive exclusion of genomic segments between sibling Drosophila species.

PubMed

Fang, Shu; Yukilevich, Roman; Chen, Ying; Turissini, David A; Zeng, Kai; Boussy, Ian A; Wu, Chung-I

2012-06-01

The extent and nature of genetic incompatibilities between incipient races and sibling species is of fundamental importance to our view of speciation. However, with the exception of hybrid inviability and sterility factors, little is known about the extent of other, more subtle genetic incompatibilities between incipient species. Here we experimentally demonstrate the prevalence of such genetic incompatibilities between two young allopatric sibling species, Drosophila simulans and D. sechellia. Our experiments took advantage of 12 introgression lines that carried random introgressed D. sechellia segments in different parts of the D. simulans genome. First, we found that these introgression lines did not show any measurable sterility or inviability effects. To study if these sechellia introgressions in a simulans background contained other fitness consequences, we competed and genetically tracked the marked alleles within each introgression against the wild-type alleles for 20 generations. Strikingly, all marked D. sechellia introgression alleles rapidly decreased in frequency in only 6 to 7 generations. We then developed computer simulations to model our competition results. These simulations indicated that selection against D. sechellia introgression alleles was high (average s = 0.43) and that the marker alleles and the incompatible alleles did not separate in 78% of the introgressions. The latter result likely implies that most introgressions contain multiple genetic incompatibilities. Thus, this study reveals that, even at early stages of speciation, many parts of the genome diverge to a point where introducing foreign elements has detrimental fitness consequences, but which cannot be seen using standard sterility and inviability assays.

A Thorium-rich Mare Basalt Rock Fragment from the Apollo 12 Regolith: A Sample from a Young Procellarum Flow?

NASA Technical Reports Server (NTRS)

Jolliff, B. L.; Zeigler, R. A.; Korotev, R. L.; Barra, F.; Swindle, T. D.

2005-01-01

In this abstract, we report on the composition, mineralogy and petrography of a basaltic rock fragment, 12032,366-18, found in the Apollo 12 regolith. Age data, collected as part of an investigation by Barra et al., will be presented in detail in. Here, only the age dating result is summarized. This rock fragment garnered our attention because it is significantly enriched in incompatible elements, e.g., 7 ppm thorium, compared to other known lunar basalts. Its mineral- and trace-element chemistry set it apart from other Apollo 12 basalts and indeed from all Apollo and Luna basalts. What makes it potentially very significant is the possibility that it is a sample of a relatively young, thorium-rich basalt flow similar to those inferred to occur in the Procellarum region, especially northwestern Procellarum, on the basis of Lunar Prospector orbital data. Exploiting the lunar regolith for the diversity of rock types that have been delivered to a landing site by impact processes and correlating them to their likely site of origin using remote sensing will be an important part of future missions to the Moon. One such mission is Moonrise, which would collect regolith samples from the South Pole-Aitken Basin, concentrating thousands of rock fragments of 3-20 mm size from the regolith, and returning the samples to Earth.

Formation and modification of chromitites in the mantle

NASA Astrophysics Data System (ADS)

Arai, Shoji; Miura, Makoto

2016-11-01

Podiform chromitites have long supplied us with unrivaled information on various mantle processes, including the peridotite-magma reaction, deep-seated magmatic evolution, and mantle dynamics. The recent discovery of ultrahigh-pressure (UHP) chromitites not only sheds light on a different aspect of podiform chromitites, but also changes our understanding of the whole picture of podiform chromitite genesis. In addition, new evidence was recently presented for hydrothermal modification/formation chromite/chromitite in the mantle, which is a classical but innovative issue. In this context, we present here an urgently needed comprehensive review of podiform chromitites in the upper mantle. Wall-rock control on podiform chromitite genesis demonstrates that the peridotite-magma reaction at the upper mantle condition is an indispensable process. We may need a large system in the mantle, far larger than the size of outcrops or mining areas, to fulfill the Cr budget requirement for podiform chromitite genesis. The peridotite-magma reaction over a large area may form a melt enriched with Na and other incompatible elements, which mixes with a less evolved magma supplied from the depth to create chromite-oversaturated magma. The incompatible-element-rich magma trapped by the chromite mainly precipitates pargasite and aspidolite (Na analogue of phlogopite), which are stable under upper mantle conditions. Moderately depleted harzburgites, which contain chromite with a moderate Cr# (0.4-0.6) and a small amount of clinopyroxene, are the best reactants for the chromitite-forming reaction, and are the best hosts for podiform chromitites. Arc-type chromitites are dominant in ophiolites, but some are of the mid-ocean ridge type; chromitites may be common beneath the ocean floor, although it has not yet been explored for chromitite. The low-pressure (upper mantle) igneous chromitites were conveyed through mantle convection or subduction down to the mantle transition zone to form ultrahigh-pressure chromitites. Some of these reappear at the shallower mantle, and can coexist with newly formed low-pressure igneous chromitites. High-temperature hydrothermal fluids can dissolve and precipitate chromite, and hydrothermal chromitites (chromitites precipitated from aqueous fluids) are possibly formed within the mantle where the circulation of hydrous fluid is available, e.g., at the mantle wedge.

Collisional stripping of planetary crusts

NASA Astrophysics Data System (ADS)

Carter, Philip J.; Leinhardt, Zoë M.; Elliott, Tim; Stewart, Sarah T.; Walter, Michael J.

2018-02-01

Geochemical studies of planetary accretion and evolution have invoked various degrees of collisional erosion to explain differences in bulk composition between planets and chondrites. Here we undertake a full, dynamical evaluation of 'crustal stripping' during accretion and its key geochemical consequences. Crusts are expected to contain a significant fraction of planetary budgets of incompatible elements, which include the major heat producing nuclides. We present smoothed particle hydrodynamics simulations of collisions between differentiated rocky planetesimals and planetary embryos. We find that the crust is preferentially lost relative to the mantle during impacts, and we have developed a scaling law based on these simulations that approximates the mass of crust that remains in the largest remnant. Using this scaling law and a recent set of N-body simulations of terrestrial planet formation, we have estimated the maximum effect of crustal stripping on incompatible element abundances during the accretion of planetary embryos. We find that on average approximately one third of the initial crust is stripped from embryos as they accrete, which leads to a reduction of ∼20% in the budgets of the heat producing elements if the stripped crust does not reaccrete. Erosion of crusts can lead to non-chondritic ratios of incompatible elements, but the magnitude of this effect depends sensitively on the details of the crust-forming melting process on the planetesimals. The Lu/Hf system is fractionated for a wide range of crustal formation scenarios. Using eucrites (the products of planetesimal silicate melting, thought to represent the crust of Vesta) as a guide to the Lu/Hf of planetesimal crust partially lost during accretion, we predict the Earth could evolve to a superchondritic 176Hf/177Hf (3-5 parts per ten thousand) at present day. Such values are in keeping with compositional estimates of the bulk Earth. Stripping of planetary crusts during accretion can lead to detectable changes in bulk composition of lithophile elements, but the fractionation is relatively subtle, and sensitive to the efficiency of reaccretion.

An Enriched Shell Element for Delamination Simulation in Composite Laminates

NASA Technical Reports Server (NTRS)

McElroy, Mark

2015-01-01

A formulation is presented for an enriched shell finite element capable of delamination simulation in composite laminates. The element uses an adaptive splitting approach for damage characterization that allows for straightforward low-fidelity model creation and a numerically efficient solution. The Floating Node Method is used in conjunction with the Virtual Crack Closure Technique to predict delamination growth and represent it discretely at an arbitrary ply interface. The enriched element is verified for Mode I delamination simulation using numerical benchmark data. After determining important mesh configuration guidelines for the vicinity of the delamination front in the model, a good correlation was found between the enriched shell element model results and the benchmark data set.

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.

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.

Chemical and mineralogical evaluation of slag products derived from the pyrolysis/melting treatment of MSW.

PubMed

Saffarzadeh, Amirhomayoun; Shimaoka, Takayuki; Motomura, Yoshinobu; Watanabe, Koichiro

2006-01-01

This paper provides the results of studies on the characteristics of novel material derived from pyrolysis/melting treatment of municipal solid waste in Japan. Slag products from pyrolysis/melting plants were sampled for the purpose of detailed phase analysis and characterization of heavy metal-containing phases using optical microscopy, electron probe microanalysis (EPMA), XRF and XRD. The study revealed that the slag material contains glass (over 95%), oxide and silicate minerals (spinel, melilite, pseudowollastonite), as well as individual metallic inclusions as the major constituents. A distinct chemical diversity was discovered in the interstitial glass in terms of silica content defined as low and high silica glass end members. Elevated concentrations of Zn, Cr, Cu, Pb and Ba were recorded in the bulk composition. Cu, Pb and Ba behave as incompatible elements since they have been markedly characterized as part of polymetallic alloys and insignificantly sulfides in the form of spherical metallic inclusions associated with tracer amounts of other elements such as Sb, Sn, Ni, Zn, Al, P and Si. In contrast, an appreciable amount of Zn is retained by zinc-rich end members of spinel and partially by melilite and silica glass. Chromium exhibits similar behavior, and is considerably held by Cr-rich spinel. The intense incorporation of Zn and Cr into spinel indicates the very effective enrichment of these two elements into phases more environmentally resistant than glass. There was no evidence, however, that Cu and Pb enter into the structure of the crystalline silicates or oxides that may lead to their easier leachability upon exposure to the environment.

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.

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.

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.

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

NASA Astrophysics Data System (ADS)

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

2018-04-01

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

Well-conditioning global-local analysis using stable generalized/extended finite element method for linear elastic fracture mechanics

NASA Astrophysics Data System (ADS)

Malekan, Mohammad; Barros, Felicio Bruzzi

2016-11-01

Using the locally-enriched strategy to enrich a small/local part of the problem by generalized/extended finite element method (G/XFEM) leads to non-optimal convergence rate and ill-conditioning system of equations due to presence of blending elements. The local enrichment can be chosen from polynomial, singular, branch or numerical types. The so-called stable version of G/XFEM method provides a well-conditioning approach when only singular functions are used in the blending elements. This paper combines numeric enrichment functions obtained from global-local G/XFEM method with the polynomial enrichment along with a well-conditioning approach, stable G/XFEM, in order to show the robustness and effectiveness of the approach. In global-local G/XFEM, the enrichment functions are constructed numerically from the solution of a local problem. Furthermore, several enrichment strategies are adopted along with the global-local enrichment. The results obtained with these enrichments strategies are discussed in detail, considering convergence rate in strain energy, growth rate of condition number, and computational processing. Numerical experiments show that using geometrical enrichment along with stable G/XFEM for global-local strategy improves the convergence rate and the conditioning of the problem. In addition, results shows that using polynomial enrichment for global problem simultaneously with global-local enrichments lead to ill-conditioned system matrices and bad convergence rate.

An enriched finite element method to fractional advection-diffusion equation

NASA Astrophysics Data System (ADS)

Luan, Shengzhi; Lian, Yanping; Ying, Yuping; Tang, Shaoqiang; Wagner, Gregory J.; Liu, Wing Kam

2017-08-01

In this paper, an enriched finite element method with fractional basis [ 1,x^{α }] for spatial fractional partial differential equations is proposed to obtain more stable and accurate numerical solutions. For pure fractional diffusion equation without advection, the enriched Galerkin finite element method formulation is demonstrated to simulate the exact solution successfully without any numerical oscillation, which is advantageous compared to the traditional Galerkin finite element method with integer basis [ 1,x] . For fractional advection-diffusion equation, the oscillatory behavior becomes complex due to the introduction of the advection term which can be characterized by a fractional element Peclet number. For the purpose of addressing the more complex numerical oscillation, an enriched Petrov-Galerkin finite element method is developed by using a dimensionless fractional stabilization parameter, which is formulated through a minimization of the residual of the nodal solution. The effectiveness and accuracy of the enriched finite element method are demonstrated by a series of numerical examples of fractional diffusion equation and fractional advection-diffusion equation, including both one-dimensional and two-dimensional, steady-state and time-dependent cases.

Sources of volatiles in basalts from the Galapagos Archipelago: deep and shallow evidence

NASA Astrophysics Data System (ADS)

Peterson, M. E.; Saal, A. E.; Hauri, E. H.; Werner, R.; Hauff, S. F.; Kurz, M. D.; Geist, D.; Harpp, K. S.

2010-12-01

The study of volatiles (H2O, CO2, F, S, and Cl) is important because volatiles assert a strong influence on mantle melting and magma crystallization, as well as on the viscosity and rheology of the mantle. Despite this importance, there have been a minimal number of volatile studies done on magmas from the four main mantle sources that define the end member compositions of the Galapagos lavas. For this reason, we here present new volatile concentrations of 89 submarine glass chips from dredges collected across the archipelago during the SONNE SO158, PLUM02, AHA-NEMO, and DRIFT04 cruises. All samples, with the exception of six, were collected at depths greater than 1000m. Major elements (E-probe), and volatile and trace elements (SIMS), are analyzed on the same glass chip, using 4 chips per sample, to better represent natural and analytical variation. Trace element contents reveal three main compositional groups: an enriched group typical of OIB, a group with intermediate compositions, and a group with a depleted trace element composition similar to MORB. The absolute ranges of volatile contents for all three compositional groups are .098-1.15wt% for H2O, 10.7-193.7 ppm for CO2, 61.4-806.5 ppm for F, 715.8-1599.2 ppm for S and 3.8-493.3 for Cl. The effect of degassing, sulfide saturation and assimilation of hydrothermally altered material must be understood before using the volatile content of submarine glasses to establish the primary volatile concentration of basalts and their mantle sources. CO2 has a low solubility in basaltic melts causing it to extensively degas. Based on the CO2/Nb ratio, we estimate the extent of degassing for the Galapagos lavas to range from approximately undegassed to 90% degassed. We demonstrate that 98% of the samples are sulfur undersaturated. Therefore, sulfur will behave as a moderately incompatible element during magmatic processes. Finally, we evaluate the effect of assimilation of hydrothermally altered material on the volatile content of the lavas. This process is evident when volatile/refractory element ratios are compared to the trace elements indicative of interaction between melt and the oceanic lithosphere such as a positive Sr anomaly (Sr*) in a primitive mantle normalized diagram. This is indicative of the interaction of basaltic melts with plagioclase cumulates. For the Galapagos depleted submarine glasses, we find a positive correlation between Sr* and all volatile/refractory element ratios suggesting significant volatile input from melt-lithosphere interaction. These samples, due to their low trace element concentrations, readily show the alteration signature, thus making the establishment of their primitive volatile content difficult. As a result, we will present the primary volatile concentrations for the trace element intermediate and enriched groups after careful consideration for degassing, sulfide saturation, and assimilation of hydrothermally altered material.

Mafic intrusion remobilising silicic magma under El Hierro, Canary Islands

NASA Astrophysics Data System (ADS)

Sigmarsson, O.; Laporte, D.; Marti, J.; Devouard, B.; Cluzel, N.

2012-04-01

The 2011 submarine eruption at El Hierro, Canary Islands, has produced volcanic bombs that degas at sea surface, boil seawater and sink when cooled and degassed. At the beginning of the eruption white coloured pumices enveloped in darker coloured spatters floated on land. These composite pumices show evidence of magma mingling with folds and undulations of the darker coloured magma within the white pumice suggesting magma mingling in a viscous regime. The white pumice is highly vesicular and resembles foam. Most of the vesicular structure is made of tightly packed, polygonal bubbles of uniform size (˜ 100 μm), suggesting a single event of homogeneous bubble nucleation. An earlier event of heterogeneous bubble nucleation is indicated by the presence of a few large bubbles developed around tiny quartz crystals. Both the darker and lighter coloured pumices are almost aphyric. A few olivine crystals with perfect euhedral morphology occur within the darker part. Rare olivines of same composition are also found in the white pumice glass but then display somewhat rounded outlines and hopper-type structure. Melt inclusions in olivines of the darker pumice are of the same composition as the enveloping mafic glass, whereas olivines in the mixing boundary layer have melt inclusions of less mafic composition. The whole-rock composition and slightly more evolved glass composition are of basanitc and alkali rhyolitic composition (at the limit of the trachyte field) according to the TAS classification. Such rhyolitic compositions are rare in the Canaries. Analyses of residual volatile concentration in the glasses show that the silicic glass is highly degassed (F: 511 ±222; Cl: 202 ±58; S: below detection limit; values in ppm,1SD, n=10), whereas the basanitic glass still has very high halogene concentrations (F: 1354 ±151; Cl: 1026 ±47; S: 362 ±29; 1SD, n=10). In-situ analysis of trace element compositions of the dark glasses reveal typical basanitic compositions with elevated incompatible element concentrations and primitive mantle normalised spectra characteristic for the Canary Island basanites (e.g. La is of 100 times higher concentration than primitive mantle with important LREE enrichments). In contrast, the trace element composition of the alkali rhyolite shows surprisingly low concentrations for all elements except the most incompatible ones (such as Rb, Ba, K and Th). All other measured incompatible LILE, HFSE and REE have significantly lower concentration than the basanitic counterpart. This differences increase with the atomic number of the REE reaching maximum for the MREE and thus forming an intriguing U-shaped rhyolite spectra. Furthermore, unusual U-depletion is observed in the rhyolite. Other negative spikes, such as those for Sr and P, are readily accounted for by the removal of plagioclase and apatite during magma evolution from a basanite to a more evolved melt. The results obtained so far suggest an intrusion of gas-rich basanitic melt at the base of an evolved intrusion remobilising a stagnant phonolitic melt present as late differentiate in the crust. Interaction with old oceanic crust and the volcanic edifice can be quantified and shown to have modified the phonolite melt composition and produced the alkali rhyolitic composition of the white floating pumice. Extensive gas exsolution shortly before the melt-glass transition explains the foam texture and the low volatile concentrations in the quenched alkali rhyolite.

Trace Elements Affect Methanogenic Activity and Diversity in Enrichments from Subsurface Coal Bed Produced Water

PubMed Central

Ünal, Burcu; Perry, Verlin Ryan; Sheth, Mili; Gomez-Alvarez, Vicente; Chin, Kuk-Jeong; Nüsslein, Klaus

2012-01-01

Microbial methane from coal beds accounts for a significant and growing percentage of natural gas worldwide. Our knowledge of physical and geochemical factors regulating methanogenesis is still in its infancy. We hypothesized that in these closed systems, trace elements (as micronutrients) are a limiting factor for methanogenic growth and activity. Trace elements are essential components of enzymes or cofactors of metabolic pathways associated with methanogenesis. This study examined the effects of eight trace elements (iron, nickel, cobalt, molybdenum, zinc, manganese, boron, and copper) on methane production, on mcrA transcript levels, and on methanogenic community structure in enrichment cultures obtained from coal bed methane (CBM) well produced water samples from the Powder River Basin, Wyoming. Methane production was shown to be limited both by a lack of additional trace elements as well as by the addition of an overly concentrated trace element mixture. Addition of trace elements at concentrations optimized for standard media enhanced methane production by 37%. After 7 days of incubation, the levels of mcrA transcripts in enrichment cultures with trace element amendment were much higher than in cultures without amendment. Transcript levels of mcrA correlated positively with elevated rates of methane production in supplemented enrichments (R2 = 0.95). Metabolically active methanogens, identified by clone sequences of mcrA mRNA retrieved from enrichment cultures, were closely related to Methanobacterium subterraneum and Methanobacterium formicicum. Enrichment cultures were dominated by M. subterraneum and had slightly higher predicted methanogenic richness, but less diversity than enrichment cultures without amendments. These results suggest that varying concentrations of trace elements in produced water from different subsurface coal wells may cause changing levels of CBM production and alter the composition of the active methanogenic community. PMID:22590465

Enrichment of intergalactic matter.

NASA Technical Reports Server (NTRS)

Silk, J.; Siluk, R. S.

1972-01-01

The primordial gas out of which the Galaxy condensed may have been significantly enriched in heavy elements. A specific mechanism of enrichment is described, in which quasi-stellar sources eject enriched matter into the intergalactic medium. This matter is recycled through successive generations of these sources, and is progressively enriched. The enriched intergalactic matter is accreted by the protogalaxy and we find, for rates of mass ejection by quasi-stellar sources equal to about one solar mass per year in heavy elements, that this mechanism can account for the heavy-element abundances in the oldest Population II stars. Expressions are given for the degree of enrichment of the intergalactic gas as a function of redshift, and we show that our hypothesis implies that the present density of intergalactic gas must be at least a factor 3 larger than the mean density in galaxies at the present epoch.

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

NASA Astrophysics Data System (ADS)

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

2018-02-01

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

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

NASA Astrophysics Data System (ADS)

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

2018-05-01

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

Variations on a Theme by Longhi: I, an Analysis of the Thermodynamic Underpinning of Fe, Mn, and Ni Partitioning into Olivine

NASA Technical Reports Server (NTRS)

Jones, John H.

2010-01-01

Longhi et al. [1] have used the D(Ni) vs. D(Mg) parameterizations of Jones [2, 3] in attempting to explain the Ni systematics of lunar differentiation. A key element of the Jones parameterization and the Longhi et al. models is that, at very high temperatures, Ni may become incompatible in olivine. Unfortunately, there is no actual experimental evidence that this is ever the case [1]. To date, all experiments designed to demonstrate such incompatibility have failed. Here I will investigate the thermodynamic foundations of the D vs. D(Mg) trends for olivine/liquid discovered by [2].

Magmatic effects of the Cobb hot spot on the Juan de Fuca Ridge

USGS Publications Warehouse

Chadwick, John; Perfit, M.; Ridley, I.; Jonasson, I.; Kamenov, G.; Chadwick, W.; Embley, R.; le, Roux P.; Smith, M.

2005-01-01

The interaction of the Juan de Fuca Ridge with the Cobb hot spot has had a considerable influence on the magmatism of the Axial Segment of the ridge, the second-order segment that overlies the hot spot. In addition to the construction of the large volcanic edifice of Axial Seamount, the Axial Segment has shallow bathymetry and a prevalence of constructional volcanic features along its 100-km length, suggesting that hot spot-derived magmas supplement and oversupply the ridge. Lavas are generally more primitive at Axial Seamount and more evolved in the Axial Segment rift zones, suggesting that fractional crystallization is enhanced with increasing distance from the hot spot because of a reduced magma supply and more rapid cooling. Although the Cobb hot spot is not an isotopically enriched plume, it produces lavas with some distinct geochemical characteristics relative to normal mid-ocean ridge basalt, such as enrichments in alkalis and highly incompatible trace elements, that can be used as tracers to identify the presence and prevalence of the hot spot influence along the ridge. These characteristics are most prominent at Axial Seamount and decline in gradients along the Axial Segment. The physical model that can best explain the geochemical observations is a scenario in which hot spot and mid-ocean ridge basalt (MORB) magmas mix to varying degrees, with the proportions controlled by the depth to the MORB source. Modeling of two-component mixing suggests that MORB is the dominant component in most Axial Segment basalts. Copyright 2005 by the American Geophysical Union.

Trace element abundances of high-MgO glasses from Kilauea, Mauna Loa and Haleakala volcanoes, Hawaii

USGS Publications Warehouse

Wagner, T.P.; Clague, D.A.; Hauri, E.H.; Grove, T.L.

1998-01-01

We performed an ion-microprobe study of eleven high-MgO (6.7-14.8 wt%) tholeiite glasses from the Hawaiian volcanoes Kilauea, Mauna Loa and Haleakala. We determined the rare earth (RE), high field strength, and other selected trace element abundances of these glasses, and used the data to establish their relationship to typical Hawaiian shield tholeiite and to infer characteristics of their source. The glasses have trace element abundance characteristics generally similar to those of typical shield tholeiites, e.g. L(light)REE/H(heavy)REE(C1) > 1. The Kilauea and Mauna Loa glasses, however, display trace and major element characteristics that cross geochemical discriminants observed between Kilauea and Mauna Loa shield lavas. The glasses contain a blend of these discriminating chemical characteristics, and are not exactly like the typical shield lavas from either volcano. The production of these hybrid magmas likely requires a complexly zoned source, rather than two unique sources. When corrected for olivine fractionation, the glass data show correlations between CaO concentration and incompatible trace element abundances, indicating that CaO may behave incompatibly during melting of the tholeiite source. Furthermore, the tholeiite source must contain residual garnet and clinopyroxene to account for the variation in trace element abundances of the Kilauea glasses. Inversion modeling indicates that the Kilauea source is flat relative to C1 chondrites, and has a higher bulk distribution coefficient for the HREE than the LREE.

Ridge suction drives plume-ridge interactions

NASA Astrophysics Data System (ADS)

Niu, Y.; Hékinian, R.

2003-04-01

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

Geochemical Diversity of the Mantle: 50 Years of Acronyms

NASA Astrophysics Data System (ADS)

Hart, S. R.

2014-12-01

50 years ago, Gast, Tilton and Hedge demonstrated that the oceanic mantle is isotopically heterogeneous. 28 years ago, Zindler and Hart formalized the concept of geochemical mantle components, with an attendant, to some, odious, acronym soup. Work on a marriage of mantle geochemistry and dynamics continues unabated. We know unequivocally that the mantle is chemically heterogeneous; we do not know the scale lengths of these heterogeneities. We know unequivocally that these heterogeneities have persisted for eons (Gy); we do not know where they were formed or where they are stored. Through the kind auspices of the Plume Model, we plausibly have access to the whole mantle. The most accessible and well understood mantle reservoir is the upper depleted MORB mantle (DMM). Classically, this mantle was depleted by extraction of oceanic and continental crust from a "chondritic" bulk silicate Earth. In this post-Boyet and Carlson world, the complementary enriched reservoir may instead be hidden in the deepest mantle. In this case, DMM will become an endangered acronym. Hofmann and White (1982) argued that radiogenic Pb mantle (HIMU) is re-cycled ocean crust, and this is a comfortably viable model. It does require some ad hoc chemical manipulations during subduction. Given 2 Gy of aggregate mantle strains, the mafic component in HIMU may be of small length scale (< 50 m), possibly subsumed into the dominant peridotitic lithology. This mantle species is globally widespread. Enriched mantles (EM1 and EM2) almost certainly reflect recycling of enriched continental material. This was splendidly verified by Jackson et al (2007), with 87Sr/86Sr in Samoan EM2 lavas up to 0.721. The lithology and length scale of EM1 and EM2 is unconstrained. EM1 is globally present; EM2 is confined to the SW Pacific hotspots. FOZO is a work in progress; many would like to see it become extinct! The trace element signatures of HIMU and FOZO mantles have been constrained using melting models; in both cases the spidergrams are "enriched" with peaks at Nb-Ta of 2x and 4x bulk silicate earth, respectively, but with quite different shapes. As is typical with OIB, the derived source compositions are incompatible with the isotopic signatures, requiring a fairly recent "enrichment" event (possibly auto-metasomatism).

The geochemistry of primitive volcanic rocks of the Ankaratra volcanic complex, and source enrichment processes in the genesis of the Cenozoic magmatism in Madagascar

NASA Astrophysics Data System (ADS)

Melluso, L.; Cucciniello, C.; le Roex, A. P.; Morra, V.

2016-07-01

The Ankaratra volcanic complex in central Madagascar consists of lava flows, domes, scoria cones, tuff rings and maars of Cenozoic age that are scattered over 3800 km2. The mafic rocks include olivine-leucite-nephelinites, basanites, alkali basalts and hawaiites, and tholeiitic basalts. Primitive samples have high Mg# (>60), high Cr and Ni concentrations; their mantle-normalized patterns peak at Nb and Ba, have troughs at K, and smoothly decrease towards the least incompatible elements. The Ankaratra mafic rocks show small variation in Sr-Nd-Pb isotopic compositions (e.g., 87Sr/86Sr = 0.70377-0.70446, 143Nd/144Nd = 0.51273-0.51280, 206Pb/204Pb = 18.25-18.87). These isotopic values differ markedly from those of Cenozoic mafic lavas of northern Madagascar and the Comoro archipelago, typical Indian Ocean MORB and oceanic basalt end-members. The patterns of olivine nephelinitic magmas can be obtained through 3-10% partial melting of a mantle source that was enriched by a Ca-rich alkaline melt, and that contained garnet, carbonates and phlogopite. The patterns of tholeiitic basalts can be obtained after 10-12% partial melting of a source enriched with lower amounts of the same alkaline melt, in the spinel- (and possibly amphibole-) facies mantle, hence in volumes where carbonate is not a factor. The significant isotopic change from the northernmost volcanic rocks of Madagascar and those in the central part of the island implicates a distinct source heterogeneity, and ultimately assess the role of the continental lithospheric mantle as source region. The source of at least some volcanic rocks of the still active Comoro archipelago may have suffered the same time-integrated geochemical and isotopic evolution as that of the northern Madagascar volcanic rocks.

Volatiles in High-K Lunar Basalts

NASA Technical Reports Server (NTRS)

Barnes, Jessica J.; McCubbin, Francis M.; Messenger, Scott R.; Nguyen, Ann; Boyce, Jeremy

2017-01-01

Chlorine is an unusual isotopic system, being essentially unfractionated ((delta)Cl-37 approximately 0 per mille ) between bulk terrestrial samples and chondritic meteorites and yet showing large variations in lunar (approximately -4 to +81 per mille), martian, and vestan (HED) samples. Among lunar samples, the volatile-bearing mineral apatite (Ca5(PO4)3[F,Cl,OH]) has been studied for volatiles in K-, REE-, and P (KREEP), very high potassium (VHK), low-Ti and high-Ti basalts, as well as samples from the lunar highlands. These studies revealed a positive correlation between in-situ (delta)Cl-37 measurements and bulk incompatible trace elements (ITEs) and ratios. Such trends were interpreted to originate from Cl isotopic fractionation during the degassing of metal chlorides during or shortly after the differentiation of the Moon via a magma ocean. In this study, we investigate the volatile inventories of a group of samples for which new-era volatile data have yet to be reported - the high-K (greater than 2000 ppm bulk K2O), high-Ti, trace element-rich mare basalts. We used isotope imaging on the Cameca NanoSIMS 50L at JSC to obtain the Cl isotopic composition [((Cl-37/(35)Clsample/C-37l/(35)Clstandard)-1)×1000, to get a value in per thousand (per mille)] which ranges from approximately -2.7 +/- 2 per mille to +16.1 +/- 2 per mille (2sigma), as well as volatile abundances (F & Cl) of apatite in samples 10017, 10024 & 10049. Simply following prior models, as lunar rocks with high bulk-rock abundances of ITEs we might expect the high-K, high-Ti basalts to contain apatite characterized by heavily fractionated (delta)Cl-37 values, i.e., Cl obtained from mixing between unfractionated mantle Cl (approximately 0 per mille) and the urKREEP reservoir (possibly fractionated to greater than +25 per mille.). However, the data obtained for the studied samples do not conform to either the early degassing or mixing models. Existing petrogentic models for the origin of the high-K, high-Ti basalts do not include urKREEP assimilation into their LMO cumulate sources. Therefore, Cl in these basalts either originated from source region heterogeneity or through assimilation or metasomatism by volatile and incompatible trace element rich materials. The new data presented here could provide evidence for the existence of region(s) in the lunar interior that are ITE-enriched and contain Cl that does not share isotopic affinities with lunar urKREEP, possibly representing the composition of the purported 'neuKREEP'.

Subduction factory in an ampoule: Experiments on sediment-peridotite interaction under temperature gradient conditions

NASA Astrophysics Data System (ADS)

Woodland, A. B.; Bulatov, V. K.; Brey, G. P.; Girnis, A. V.; Höfer, H. E.; Gerdes, A.

2018-02-01

To better understand processes above subducted oceanic slabs, we have undertaken experiments with juxtaposed sediment and peridotite layers at pressures of 7.5 and 10.5 GPa at a controlled temperature gradient from ∼100 to ∼500 °C per a sample length of ∼3 mm. The sediment starting material contains H2O (6.9 wt%) and CO2 (5.9 wt%) and has a major-element composition similar to GLOSS (Plank and Langmuir, 1998) doped with trace elements at 10-100 ppm levels. Several experiments were conducted with ∼0.5 wt% Cl or F. The peridotite layer is composed of natural olivine (66 wt%), orthopyroxene (27 wt%) and garnet (7 wt%) mixed with ∼15 wt% graphite. Several experimental configurations were investigated, but the "basic" setup has the sediment layer at the bottom in the cold zone (400-1200 °C) overlain by peridotite at 900-1500 °C. The temperature distribution was determined by two thermocouples and orthopyroxene-garnet thermometry. Features common to many experiments are (1) the development of multiple layers of various lithologies and a pool of hydrous silicate or carbonate-silicate melt in the hottest part of the capsule; (2) replacement of olivine by orthopyroxene in the metaperidotite; (3) preservation and growth of garnet and local development of magnesite in the metaperidotite layer; (4) enrichment in garnet within the metasediment layer at the contact with the metaperidotite; (5) formation of a clinopyroxene-garnet assemblage at the bottom (the coldest part); (6) presence of K-bearing phases (phlogopite or phengite) and carbonates in the metasediment layer only at temperatures <700 °C; and (7) occurrence of accessory zircon, rutile and phosphates in the coldest regions. In terms of element redistribution, the peridotite becomes strongly enriched in SiO2 compared to the starting composition, and the sediment gains MgO, FeO and Cr2O3. Potassium is fully extracted into the melt, while Na and Ca are largely retained in the coldest part of the metasediment layer in clinopyroxene, Ca-rich garnet and aragonite. The melt is a product of interaction between partial melt or fluid from the sediment and peridotite. It has a silico-carbonatite composition with variable SiO2, MgO, FeO and CaO contents and low Al2O3. The addition of Cl has almost no effect on element distribution, whereas the addition of F results in the appearance of humite-group minerals containing significant amounts of Ti. Trace-element distribution is controlled by pressure, temperature and mineral assemblages. At low temperatures in the sediment layer (<700 °C) Ba, Rb, Sr and Li are much more mobile than REE and HFSE, which results in high Ba/La, Ba/Nb, Sr/Nb etc. (fluid metasomatism). At higher temperatures in the sediment layer, the melt is markedly enriched in Ba, Rb, Sr, LREE and U relative to Ti, MREE and HREE. Negative Nb-Ta and Zr-Hf anomalies in melts are caused by the retention of rutile, zircon and humite-group minerals in the solid residue. Thermodiffusion may affect the ratios of some highly incompatible elements (e.g., Ta/La). Possible applications of the results to natural deep subduction are discussed in view of variations in mineral assemblages and trace element ratios.

Production test IP-544-A, irradiation of 1.6% enriched thick walled single tube elements in KER-1 and 2

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

Kratzer, W.K.; Wise, M.J.

1962-12-12

The objective of this production test is to authorize the irradiation of coextruded Zr-2 jacketed thick walled 1.6% enriched tubular elements in KER loops 1 and 2 to evaluate the swelling behavior of fuel elements at high uranium temperatures Coextruded Zr-2 jacketed 1.6% enriched tubular fuel elements 1.79 inch OD, 0.97 inch ID, and 12 inches long will be irradiated KER loops 1 and 2 to exposures no greater than 2500 MWD/T.

Alkali trace elements in Gale crater, Mars, with ChemCam: Calibration update and geological implications

NASA Astrophysics Data System (ADS)

Payré, V.; Fabre, C.; Cousin, A.; Sautter, V.; Wiens, R. C.; Forni, O.; Gasnault, O.; Mangold, N.; Meslin, P.-Y.; Lasue, J.; Ollila, A.; Rapin, W.; Maurice, S.; Nachon, M.; Le Deit, L.; Lanza, N.; Clegg, S.

2017-03-01

The Chemistry Camera (ChemCam) instrument onboard Curiosity can detect minor and trace elements such as lithium, strontium, rubidium, and barium. Their abundances can provide some insights about Mars' magmatic history and sedimentary processes. We focus on developing new quantitative models for these elements by using a new laboratory database (more than 400 samples) that displays diverse compositions that are more relevant for Gale crater than the previous ChemCam database. These models are based on univariate calibration curves. For each element, the best model is selected depending on the results obtained by using the ChemCam calibration targets onboard Curiosity. New quantifications of Li, Sr, Rb, and Ba in Gale samples have been obtained for the first 1000 Martian days. Comparing these data in alkaline and magnesian rocks with the felsic and mafic clasts from the Martian meteorite NWA7533—from approximately the same geologic period—we observe a similar behavior: Sr, Rb, and Ba are more concentrated in soluble- and incompatible-element-rich mineral phases (Si, Al, and alkali-rich). Correlations between these trace elements and potassium in materials analyzed by ChemCam reveal a strong affinity with K-bearing phases such as feldspars, K-phyllosilicates, and potentially micas in igneous and sedimentary rocks. However, lithium is found in comparable abundances in alkali-rich and magnesium-rich Gale rocks. This very soluble element can be associated with both alkali and Mg-Fe phases such as pyroxene and feldspar. These observations of Li, Sr, Rb, and Ba mineralogical associations highlight their substitution with potassium and their incompatibility in magmatic melts.

Derivation of Apollo 14 High-Al Basalts at Discrete Times: Rb-Sr Isotopic Constraints

NASA Technical Reports Server (NTRS)

Hui. Hejiu; Neal, Clive, R.; Shih, Chi-Yu; Nyquist, Laurence E.

2012-01-01

Pristine Apollo 14 (A-14) high-Al basalts represent the oldest volcanic deposits returned from the Moon [1,2] and are relatively enriched in Al2O3 (>11 wt%) compared to other mare basalts (7-11 wt%). Literature Rb-Sr isotopic data suggest there are at least three different eruption episodes for the A-14 high-Al basalts spanning the age range approx.4.3 Ga to approx.3.95 Ga [1,3]. Therefore, the high-Al basalts may record lunar mantle evolution between the formation of lunar crust (approx.4.4 Ga) and the main basin-filling mare volcanism (<3.85 Ga) [4]. The high-Al basalts were originally classified into five compositional groups [5,6], and then regrouped into three with a possible fourth comprising 14072 based on the whole-rock incompatible trace element (ITE) ratios and Rb-Sr radiometric ages [7]. However, Rb-Sr ages of these basalts from different laboratories may not be consistent with each other because of the use of different 87Rb decay constants [8] and different isochron derivation methods over the last four decades. This study involved a literature search for Rb-Sr isotopic data previously reported for the high-Al basalts. With the re-calculated Rb-Sr radiometric ages, eruption episodes of A-14 high-Al basalts were determined, and their petrogenesis was investigated in light of the "new" Rb-Sr isotopic data and published trace element abundances of these basalts.

Lunar mare volcanism: Mixing of distinct, mantle source regions with KREEP-like component

NASA Technical Reports Server (NTRS)

Shervais, John W.; Vetter, Scott K.

1993-01-01

Mare basalts comprise less than 1% of the lunar crust, but they constitute our primary source of information on the moon's upper mantle. Compositional variations between mare basalt suites reflect variations in the mineralogical and geochemical composition of the lunar mantle which formed during early lunar differentiation (4.5-4.4 AE). Three broad suites of mare basalt are recognized: very low-Ti (VLT) basalts with TiO2 less than 1 wt%, low-Ti basalts with TiO2 = 2-4 wt%, and high-Ti basalts with TiO2 = 10-14 wt%. Important subgroups include the Apollo 12 ilmenite basalts (TiO2 = 5-6 wt%), aluminous low-Ti mare basalts (TiO2 = 2-4 wt%, Al2O3 = 10-14 wt%), and the newly discovered Very High potassium (VHK) aluminous low-Ti basalts, with K2O = 0.4-1.5 wt%. The mare basalt source region has geochemical characteristics complementary to the highlands crust and is generally thought to consist of mafic cumulates from the magma ocean which formed the felsic crust by feldspar flotation. The progressive enrichment of mare basalts in Fe/Mg, alkalis, and incompatible trace elements in the sequence VLT basalt yields low-Ti basalt yields high-Ti basalt is explained by the remelting of mafic cumulates formed at progressively shallower depths in the evolving magma ocean. This model is also consistent with the observed decrease in compatible element concentrations and the progressive increase in negative Eu anomalies.

Siderophile and chalcophile element abundances in oceanic basalts, Pb isotope evolution and growth of the earth's core

NASA Technical Reports Server (NTRS)

Newsom, H. E.; White, W. M.; Jochum, K. P.; Hofmann, A. W.

1986-01-01

The hypothesis that the mantle Pb isotope ratios reflect continued extraction of Pb into the earth's core over geologic time is evaluated by studying the depeletion of chalcophile and siderophile elements in the mantle. Oceanic basalt samples are analyzed in order to determine the Pb, Sr, and Nd isotropic compositions and the abundances of siderophile and chalcophile elements and incompatible lithophile elements. The data reveal that there is no systematic variation of siderophile or chalcophile element abundances relative to abundances of lithophile elements and the Pb/Ce ratio of the mantle is constant. It is suggested that the crust formation involves nonmagmatic and magmatic processes.

Constraints on the magmatic evolution of the oceanic crust from plagiogranite intrusions in the Oman ophiolite

NASA Astrophysics Data System (ADS)

Haase, Karsten M.; Freund, Sarah; Beier, Christoph; Koepke, Jürgen; Erdmann, Martin; Hauff, Folkmar

2016-05-01

We present major and trace element as well as Sr, Nd, and Hf isotope data on a suite of 87 plutonic rock samples from 27 felsic crustal intrusions in seven blocks of the Oman ophiolite. The rock compositions of the sample suite including associated more mafic rocks range from 48 to 79 wt% SiO2, i.e. from gabbros to tonalites. The samples are grouped into a Ti-rich and relatively light rare earth element (LREE)-enriched P1 group [(Ce/Yb) N > 0.7] resembling the early V1 lavas, and a Ti-poor and LREE-depleted P2 group [(Ce/Yb) N < 0.7] resembling the late-stage V2 lavas. Based on the geochemical differences and in agreement with previous structural and petrographic models, we define phase 1 (P1) and phase 2 (P2) plutonic rocks. Felsic magmas in both groups formed by extensive fractional crystallization of olivine, clinopyroxene, plagioclase, apatite, and Ti-magnetite from mafic melts. The incompatible element compositions of P1 rocks overlap with those from mid-ocean ridges but have higher Ba/Nb and Th/Nb trending towards the P2 rock compositions and indicating an influence of a subducting slab. The P2 rocks formed from a more depleted mantle source but show a more pronounced slab signature. These rocks also occur in the southern blocks (with the exception of the Tayin block) of the Oman ophiolite implying that the entire ophiolite formed above a subducting slab. Initial Nd and Hf isotope compositions suggest an Indian-MORB-type mantle source for the Oman ophiolite magmas. Isotope compositions and high Th/Nb in some P2 rocks indicate mixing of a melt from subducted sediment into this mantle.

Episodic trace element and isotopic variations in historical Mauna Loa Lavas: Implications for magma and plume dynamics

NASA Astrophysics Data System (ADS)

Rhodes, J. M.; Hart, S. R.

Over the past 152 years, Mauna Loa volcano has erupted lavas with almost constant major element, and compatible and moderately incompatible trace element abundances at a given MgO content. This uniformity is attributed to continuing replenishment of a shallow magma reservoir. In contrast, incompatible element abundances and ratios, together with Sr, Nd and Pb isotopic ratios, vary systematically with time. The greatest rate of change occurred at a time (1843-1887) when Mauna Loa was vigorously active with high eruption rates, presumably a consequence of a high magma supply rate. Detailed analysis confirms what is evident from the isotopic data: that this open-system magmatism requires two or more parental magmas. One has the compositional attributes of lavas erupted in 1843, the other the characteristics of lavas erupted at the summit early in 1880. All other historical lavas can be considered as mixtures of these two end-members, modified by contemporaneous eruption and olivine crystallization. Both parental magmas have Sr, Pb and Nd isotopic ratios typical of magmas in the Hawaiian tholeiitic array, and intermediate between those of Kilauea and Koolau lavas, the end-members of the array. The 1843 parental magma has incompatible element ratios that are similar to, and overlap with the Koolau and Kilauea data. The inferred 1880 parental magma, however, is more depleted than the 1843 parental magma (and most other Hawaiian lavas), and is also isotopically closer to the Kilauea end-member of the tholeiitic array. The origin of these parental magmas is discussed in terms of melting within a radially heterogeneous plume in which the heterogeneity may develop at the source or through subsequent mantle entrainment. Two models are explored, both depend on the location of Mauna Loa at, or close to the plume margin. In the simplest case the parental magmas are produced by progressive melting of the heterogeneous outer plume. The second model is more dynamic, involving melt production and re-equilibration in a diverging, or inclined, plume.

Selfish genetic elements and sexual selection: their impact on male fertility.

PubMed

Price, Tom A R; Wedell, Nina

2008-03-01

Females of many species mate with more than one male (polyandry), yet the adaptive significance of polyandry is poorly understood. One hypothesis to explain the widespread occurrence of multiple mating is that it may allow females to utilize post-copulatory mechanisms to reduce the risk of fertilizing their eggs with sperm from incompatible males. Selfish genetic elements (SGEs) are ubiquitous in eukaryotes, frequent sources of reproductive incompatibilities, and associated with fitness costs. However, their impact on sexual selection is largely unexplored. In this review we examine the link between SGEs, male fertility and sperm competitive ability. We show there is widespread evidence that SGEs are associated with reduced fertility in both animals and plants, and present some recent data showing that males carrying SGEs have reduced paternity in sperm competition. We also discuss possible reasons why male gametes are particularly vulnerable to the selfish actions of SGEs. The widespread reduction in male fertility caused by SGEs implies polyandry may be a successful female strategy to bias paternity against SGE-carrying males.

Selfish genetic elements and sexual selection: their impact on male fertility.

PubMed

Price, Tom A R; Wedell, Nina

2008-09-01

Females of many species mate with more than one male (polyandry), yet the adaptive significance of polyandry is poorly understood. One hypothesis to explain the widespread occurrence of multiple mating is that it may allow females to utilize post-copulatory mechanisms to reduce the risk of fertilizing their eggs with sperm from incompatible males. Selfish genetic elements (SGEs) are ubiquitous in eukaryotes, frequent sources of reproductive incompatibilities, and associated with fitness costs. However, their impact on sexual selection is largely unexplored. In this review we examine the link between SGEs, male fertility and sperm competitive ability. We show there is widespread evidence that SGEs are associated with reduced fertility in both animals and plants, and present some recent data showing that males carrying SGEs have reduced paternity in sperm competition. We also discuss possible reasons why male gametes are particularly vulnerable to the selfish actions of SGEs. The widespread reduction in male fertility caused by SGEs implies polyandry may be a successful female strategy to bias paternity against SGE-carrying males.

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

NASA Astrophysics Data System (ADS)

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

2016-12-01

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

Macroarray expression analysis of barley susceptibility and nonhost resistance to Blumeria graminis.

PubMed

Eichmann, Ruth; Biemelt, Sophia; Schäfer, Patrick; Scholz, Uwe; Jansen, Carin; Felk, Angelika; Schäfer, Wilhelm; Langen, Gregor; Sonnewald, Uwe; Kogel, Karl-Heinz; Hückelhoven, Ralph

2006-04-01

Different formae speciales of the grass powdery mildew fungus Blumeria graminis undergo basic-compatible or basic-incompatible (nonhost) interactions with barley. Background resistance in compatible interactions and nonhost resistance require common genetic and mechanistic elements of plant defense. To build resources for differential screening for genes that potentially distinguish a compatible from an incompatible interaction on the level of differential gene expression of the plant, we constructed eight dedicated cDNA libraries, established 13.000 expressed sequence tag (EST) sequences and designed DNA macroarrays. Using macroarrays based on cDNAs derived from epidermal peels of plants pretreated with the chemical resistance activating compound acibenzolar-S-methyl, we compared the expression of barley gene transcripts in the early host interaction with B. graminis f.sp. hordei or the nonhost pathogen B. graminis f.sp. tritici, respectively. We identified 102 spots corresponding to 94 genes on the macroarray that gave significant B. graminis-responsive signals at 12 and/or 24 h after inoculation. In independent expression analyses, we confirmed the macroarray results for 11 selected genes. Although the majority of genes showed a similar expression profile in compatible versus incompatible interactions, about 30 of the 94 genes were expressed on slightly different levels in compatible versus incompatible interactions.

Selfish evolution of cytonuclear hybrid incompatibility in Mimulus

PubMed Central

Finseth, Findley R.; Barr, Camille M.; Fishman, Lila

2016-01-01

Intraspecific coevolution between selfish elements and suppressors may promote interspecific hybrid incompatibility, but evidence of this process is rare. Here, we use genomic data to test alternative models for the evolution of cytonuclear hybrid male sterility in Mimulus. In hybrids between Iron Mountain (IM) Mimulus guttatus × Mimulus nasutus, two tightly linked M. guttatus alleles (Rf1/Rf2) each restore male fertility by suppressing a local mitochondrial male-sterility gene (IM-CMS). Unlike neutral models for the evolution of hybrid incompatibility loci, selfish evolution predicts that the Rf alleles experienced strong selection in the presence of IM-CMS. Using whole-genome sequences, we compared patterns of population-genetic variation in Rf at IM to a neighbouring population that lacks IM-CMS. Consistent with local selection in the presence of IM-CMS, the Rf region shows elevated FST, high local linkage disequilibrium and a distinct haplotype structure at IM, but not at Cone Peak (CP), suggesting a recent sweep in the presence of IM-CMS. In both populations, Rf2 exhibited lower polymorphism than other regions, but the low-diversity outliers were different between CP and IM. Our results confirm theoretical predictions of ubiquitous cytonuclear conflict in plants and provide a population-genetic mechanism for the evolution of a common form of hybrid incompatibility. PMID:27629037

Selfish evolution of cytonuclear hybrid incompatibility in Mimulus.

PubMed

Case, Andrea L; Finseth, Findley R; Barr, Camille M; Fishman, Lila

2016-09-14

Intraspecific coevolution between selfish elements and suppressors may promote interspecific hybrid incompatibility, but evidence of this process is rare. Here, we use genomic data to test alternative models for the evolution of cytonuclear hybrid male sterility in Mimulus In hybrids between Iron Mountain (IM) Mimulus guttatus × Mimulus nasutus, two tightly linked M. guttatus alleles (Rf1/Rf2) each restore male fertility by suppressing a local mitochondrial male-sterility gene (IM-CMS). Unlike neutral models for the evolution of hybrid incompatibility loci, selfish evolution predicts that the Rf alleles experienced strong selection in the presence of IM-CMS. Using whole-genome sequences, we compared patterns of population-genetic variation in Rf at IM to a neighbouring population that lacks IM-CMS. Consistent with local selection in the presence of IM-CMS, the Rf region shows elevated FST, high local linkage disequilibrium and a distinct haplotype structure at IM, but not at Cone Peak (CP), suggesting a recent sweep in the presence of IM-CMS. In both populations, Rf2 exhibited lower polymorphism than other regions, but the low-diversity outliers were different between CP and IM. Our results confirm theoretical predictions of ubiquitous cytonuclear conflict in plants and provide a population-genetic mechanism for the evolution of a common form of hybrid incompatibility. © 2016 The Author(s).

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.

Computational methods for global/local analysis

NASA Technical Reports Server (NTRS)

Ransom, Jonathan B.; Mccleary, Susan L.; Aminpour, Mohammad A.; Knight, Norman F., Jr.

1992-01-01

Computational methods for global/local analysis of structures which include both uncoupled and coupled methods are described. In addition, global/local analysis methodology for automatic refinement of incompatible global and local finite element models is developed. Representative structural analysis problems are presented to demonstrate the global/local analysis methods.

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

NASA Astrophysics Data System (ADS)

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

2012-12-01

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

As, Bi, Hg, S, Sb, Sn and Te geochemistry of the J-M Reef, Stillwater Complex, Montana: constraints on the origin of PGE-enriched sulfides in layered intrusions

USGS Publications Warehouse

Zientek, M.L.; Fries, T.L.; Vian, R.W.

1990-01-01

The J-M Reef is an interval of disseminated sulfides in the Lower Banded series of the Stillwater Complex that is enriched in the platinum group elements (PGE). Palladium and Pt occur in solid solution in base-metal sulfides and as discrete PGE minerals. PGE minerals include sulfides, tellurides, arsenides, antimonides, bismuthides, and alloys with Fe, Sn, Hg, and Au. Several subpopulations can be delineated based on whole-rock chemical analyses for As, Bi, Cu, Hg, Pd, Pt, S, Sb and Te for samples collected from and adjacent to the J-M Reef. In general, samples from within the reef have higher Pt/Cu, Pd/Cu, Pd/Pt, Te/Bi and S/(Te+Bi) than those collected adjacent to the reef. Vertical compositional profiles through the reef suggest that Pd/Cu and Pt/Cu decrease systematically upsection from mineralized to barren rock. The majority of samples with elevated As, Sb and Hg occur adjacent to the reef, not within it, or in sulfide-poor rocks. Neither magma mixing nor fluid migration models readily explain why the minor quantities of sulfide minerals immediately adjacent to the sulfide-enriched layers that form the J-M Reef have different element ratios than the sulfide minerals that form the reef. If all the sulfides formed by exsolution during a magma mixing event and the modal proportion of sulfide now in the rocks are simply the result of mechanical processes that concentrated the sulfides into some layers and not others, then the composition of the sulfide would not be expected to be different. Models that rely upon ascending liquids or fluids are incompatible with the presence of sulfides that are not enriched in PGE immediately below or interlayered with the PGE-enriched sulfides layers. PGE-enriched postcumulus fluids should have reacted to the same extent with sulfides immediately outside the reef as within the reef. One explanation is that some of the sulfide minerals in the rocks outside the reef have a different origin than those that make up the reef. The sulfide minerals that form the reef may represent a cumulus sulfide phase that formed as the result of a magma-mixing event, achieved its high PGE contents at that time, and accumulated to form a layer. The rocks outside the reef may contain a large proportion of postcumulus sulfide minerals that formed as the last dregs of intercumulus liquids trapped in the interstitial spaces between the cumulus grains reached sulfur saturation and exsolved a sulfide liquid or precipitated a sulfide mineral. The PGE contents of these sulfides would be expected to be less than the cumulus sulfides that form the reef since they would have equilibrated with a much smaller volume of silicate liquid. Another explanation is that some of the sulfide droplets that formed as a result of the mixing event were trapped as inclusions in silicate minerals soon after they formed. This would reduce the amount of magma these sulfide droplets could equilibrate with and effectively reduce their PGE tenor. ?? 1990.

How does recycling of sediment components in arc magmatism really work?

NASA Astrophysics Data System (ADS)

Kelemen, P.; Hacker, B.; Austin, N.

2007-12-01

Past work indicates substantial recycling of a sediment component rich in LILE, Th, Sr, Pb and LREE in arcs. For example, in the relatively well-constrained case of Central America, Plank et al (Geology 02) estimate that 80% of subducted, sedimentary Th is recycled in arc magmas. To understand how such a component is transferred from subducted sediment to arc lava, we examined trace-element variation in (a) mid-crustal (0.4 GPa) contact metamorphic rocks (Austin & Kelemen, Fall 06 AGU) and (b) ultrahigh-pressure (UHP, > 3 GPa) metasediments. Most UHP samples were metamorphosed along subduction-zone geotherms (Hacker, Int Geol Rev 06), but some record substantially higher T (e.g., Erzgebirge & Kokchetav, Massone EPSL 03). Unmelted, mid-crustal metapelites are indistinguishable from pelitic sediments for the entire suite of elements analyzed by ICP-MS at WSU. Melt extraction from the mid-crustal metapelites led to systematic depletion of incompatible elements in high-grade hornfels. Depletion increases with decreasing distance to the contact with a mafic pluton, most clearly at peak T > 750°C. In contrast, although many UHP metapelites record PT above the aqueous fluid-saturated solidus, and have fluid inclusions and/or hydrous phases, compared to pelites they show no detectable depletion of "fluid-mobile" elements such as LILE (Cs, Rb, Ba, U, K), Sr and Pb, no depletion of "fluid-immobile, incompatible" elements such as Th and LREE, and no systematic change in key soluble/insoluble ratios such as Ba/Th or K/Zr up to ~1000 C. Mobility of incompatible elements is evident for T > 1000 C, well above PT for subduction-zone geotherms. Presumably, trace phases rich in LILE, Th and LREE persist to ~1050 C in metapelites at UHP conditions.How can our observations be reconciled with the recycled sediment component in arc lavas? Our preferred hypothesis is that low-density metasediments rise into the mantle wedge when heating yields viscosities low enough for density-driven instabilities (Ringwood JGSL 74; Marsh AJS 76; Gerya & Yuen EPSL 03; Kelemen et al, Treatise on Geochem 03). In the wedge, metasedimentary diapirs heat as they rise, and undergo large degrees of super-adiabatic partial melting which exhaust trace phases, releasing the sediment component observed in arcs.

Anthropophile elements in river sediments: Overview from the Seine River, France

NASA Astrophysics Data System (ADS)

Chen, Jiu-Bin; Gaillardet, Jérôme; Bouchez, Julien; Louvat, Pascale; Wang, Yi-Na

2014-11-01

In contrast to larger river systems that drain relatively pristine basins, little is known about the sediment geochemistry of rivers impacted by intense human activities. In this paper, we present a systematic investigation of the anthropogenic overprints on element geochemistry in sediments of the human-impacted Seine River, France. Most elements are fractionated by grain size, as shown by the comparison between suspended particulate matter (SPM) and riverbank deposits (RBD). The RBD are particularly coarse and enriched in carbonates and heavy minerals and thus in elements such as Ba, Ca, Cr, Hf, Mg, Na, REEs, Sr, Ti, Th, and Zr. Although the enrichment/depletion pattern of some elements (e.g., K, REEs, and Zr) can largely be explained by a binary mixture between two sources, other elements such as Ag, Bi, Cr, Cd, Co, Cu, Fe, Mo, Ni, Pb, Sb, Sn, W, and Zn in SPM in Paris show that a third end-member having anthropogenic characteristics is needed to account for their enrichment at low water stage. These "anthropophile" elements, with high enrichment factors (EFs) relative to the upper continental crust (UCC), display a progressive enrichment downstream and different geochemical behaviors with respect to the hydrodynamic conditions (e.g., grain size) compared to elements having mainly a natural origin. Our findings emphasize the need for systematic studies of these anthropophile elements in other human-impacted rivers using geochemical normalization techniques, and stress the importance of studying the chemical variability associated with hydrodynamic conditions when characterizing riverine element geochemistry and assessing their flux to the ocean.

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.

Silicic melt evolution in the early Izu-Bonin arc recorded in detrital zircons: Zircon U-Pb geochronology and trace element geochemistry for Site U1438, Amami Sankaku Basin

NASA Astrophysics Data System (ADS)

Barth, A. P.; Tani, K.; Meffre, S.; Wooden, J. L.; Coble, M. A.

2016-12-01

Understanding the petrologic evolution of oceanic arc magmas through time is important because these arcs reveal the processes of formation and the early evolution of juvenile continental crust. The Izu-Bonin (IB) arc system has been targeted because it is one of several western Pacific intraoceanic arcs initiated at 50 Ma and because of its prominent spatial asymmetry, with widespread development of relatively enriched rear arc lavas. We examined Pb/U and trace element compositions in zircons recovered at IODP Site 351-U1438 and compared them to regional and global zircon suites. These new arc zircon data indicate that detrital zircons will yield new insights into the generation of IB silicic melts and form a set of useful geochemical proxies for interpreting ancient arc detrital zircon provenance. Project IBM drilling target IBM1 was explored by Expedition 351 at Site U1438, located in the proximal back-arc of the northern Kyushu-Palau Ridge (KPR) at 27.3°N. A 1.2 km thick section of Paleogene volcaniclastic rocks, increasingly lithified and hydrothermally altered with depth, constitutes a proximal rear arc sedimentary record of IB arc initiation and early arc evolution. The ages and compositions of U1438 zircons are compatible with provenance in one or more edifices of the northern KPR and are incompatible with drilling contamination. Melt zircon saturation temperatures and Ti-in-zircon thermometry suggest a provenance in relatively cool and silicic KPR melts. The abundances of selected trace elements with high native concentrations provide insight into the petrogenesis of U1438 detrital zircon host melts, and may be useful indicators of both short and long-term variations in melt compositions in arc settings. The U1438 zircons are slightly enriched in U and LREE and are depleted in Nb compared to zircons from mid-ocean ridges and the Parece-Vela Basin, as predicted for melts in a primitive oceanic arc setting with magmas derived from a highly depleted mantle source. Close age and geochemical affinity of U1438 detrital zircons to igneous zircons in Eocene leucotonalite from the partially exhumed intrusive suite at Komahashi-Daini Seamount in the northernmost KPR suggests that these zircons also can yield insight into the link between silicic volcanism and evolving tonalitic intrusions in the Paleogene IB arc.

An olivine-free mantle lithology as a source for mantle-derived magmas: the role of metasomes in the Ethiopian-Arabian large igneous province.

NASA Astrophysics Data System (ADS)

Rooney, T. O.; Nelson, W. R.; Ayalew, D.; Yirgu, G.; Herzberg, C. T.; Hanan, B. B.

2014-12-01

Peridotite constitutes most of the Earth's upper mantle, and it is therefore unsurprising that most mantle-derived magmas exhibit evidence of past equilibrium with olivine-dominated source. There is mounting evidence, however, for the role of pyroxenite in magma generation within upwelling mantle plumes; a less documented non-peridotite source of melts are metasomatic veins (metasomes) within the lithospheric mantle. Melts derived from metasomes may exhibit extreme enrichment or depletion in major and trace elements. We hypothesize that phenocrysts such as olivine, which are commonly used to probe basalt source lithology, will reflect these unusual geochemical signals. Here we present preliminary major and trace element analyses of 60 lavas erupted from a small Miocene shield volcano located within the Ethiopian flood basalt province. Erupted lavas are intercalated with lahars and pyroclastic horizons that are overlain by a later stage of activity manifested in small cinder cones and flows. The lavas form two distinctive petrographic and geochemical groups: (A) an olivine-phyric, low Ti group (1.7-2.7 wt. % TiO2; 4.0-13.6 wt. % MgO), which geochemically resembles most of the basalts in the region. These low Ti lavas are the only geochemical unit identified in the later cinder cones and associated lava flows. (B) a clinopyroxene-phyric high Ti group (1-6.7 wt. % TiO2; 1.0-9.5 wt. % MgO), which resembles the Oligocene HT-2 flood basalts. This unit is found intercalated with low Ti lavas within the Miocene shield. In comparison to the low Ti group, the high Ti lavas exhibit a profound depletion in Ni, Cr, Al, and Si, and significant enrichment in Ca, Fe, V, and the most incompatible trace elements. When combined with a diagnostic negative K anomaly in primitive-mantle normalized diagrams and Na2O>K2O, the geochemical data point towards a source which is rich in amphibole, devoid of olivine, and perhaps containing some carbonate. Our preliminary results have identified a large suite of primitive lavas derived from a nominally olivine-free mantle source. Consequently, our future work will examine olivine geochemical characteristics and constrain the compositional space for these unusual mantle lithologies.

Depleted arc volcanism in the Alboran Sea and shoshonitic volcanism in Morocco: geochemical and isotopic constraints on Neogene tectonic processes

NASA Astrophysics Data System (ADS)

Gill, R. C. O.; Aparicio, A.; El Azzouzi, M.; Hernandez, J.; Thirlwall, M. F.; Bourgois, J.; Marriner, G. F.

2004-12-01

Samples of volcanic rocks from Alborán Island, the Alboran Sea floor and from the Gourougou volcanic centre in northern Morocco have been analyzed for major and trace elements and Sr-Nd isotopes to test current theories on the tectonic geodynamic evolution of the Alboran Sea. The Alborán Island samples are low-K tholeiitic basaltic andesites whose depleted contents of HFS elements (˜0.5×N-MORB), especially Nb (˜0.2×N-MORB), show marked geochemical parallels with volcanics from immature intra-oceanic arcs and back-arc basins. Several of the submarine samples have similar compositions, one showing low-Ca boninite affinity. 143Nd/ 144Nd ratios fall in the same range as many island-arc and back-arc basin samples, whereas 87Sr/ 86Sr ratios (on leached samples) are somewhat more radiogenic. Our data point to active subduction taking place beneath the Alboran region in Miocene times, and imply the presence of an associated back-arc spreading centre. Our sea floor suite includes a few more evolved dacite and rhyolite samples with ( 87Sr/ 86Sr) 0 up to 0.717 that probably represent varying degrees of crustal melting. The shoshonite and high-K basaltic andesite lavas from Gourougou have comparable normalized incompatible-element enrichment diagrams and Ce/Y ratios to shoshonitic volcanics from oceanic island arcs, though they have less pronounced Nb deficits. They are much less LIL- and LREE-enriched than continental arc analogues and post-collisional shoshonites from Tibet. The magmas probably originated by melting in subcontinental lithospheric mantle that had experienced negligible subduction input. Sr-Nd isotope compositions point to significant crustal contamination which appears to account for the small Nb anomalies. The unmistakable supra-subduction zone (SSZ) signature shown by our Alboran basalts and basaltic andesite samples refutes geodynamic models that attribute all Neogene volcanism in the Alboran domain to decompression melting of upwelling asthenosphere arising from convective thinning of over-thickened lithosphere. Our data support recent models in which subsidence is caused by westward rollback of an eastward-dipping subduction zone beneath the westernmost Mediterranean. Moreover, severance of the lithosphere at the edges of the rolling-back slab provides opportunities for locally melting lithospheric mantle, providing a possible explanation for the shoshonitic volcanism seen in northern Morocco and more sporadically in SE Spain.

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).

Alkali trace elements in Gale crater, Mars, with ChemCam: Calibration update and geological implications

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

Payre, Valerie; Fabre, Cecile; Cousin, Agnes

The Chemistry Camera (ChemCam) instrument onboard Curiosity can detect minor and trace elements such as lithium, strontium, rubidium, and barium. Their abundances can provide some insights about Mars' magmatic history and sedimentary processes. We focus on developing new quantitative models for these elements by using a new laboratory database (more than 400 samples) that displays diverse compositions that are more relevant for Gale crater than the previous ChemCam database. These models are based on univariate calibration curves. For each element, the best model is selected depending on the results obtained by using the ChemCam calibration targets onboard Curiosity. New quantificationsmore » of Li, Sr, Rb, and Ba in Gale samples have been obtained for the first 1000 Martian days. Comparing these data in alkaline and magnesian rocks with the felsic and mafic clasts from the Martian meteorite NWA7533—from approximately the same geologic period—we observe a similar behavior: Sr, Rb, and Ba are more concentrated in soluble- and incompatible-element-rich mineral phases (Si, Al, and alkali-rich). Correlations between these trace elements and potassium in materials analyzed by ChemCam reveal a strong affinity with K-bearing phases such as feldspars, K-phyllosilicates, and potentially micas in igneous and sedimentary rocks. However, lithium is found in comparable abundances in alkali-rich and magnesium-rich Gale rocks. This very soluble element can be associated with both alkali and Mg-Fe phases such as pyroxene and feldspar. Here, these observations of Li, Sr, Rb, and Ba mineralogical associations highlight their substitution with potassium and their incompatibility in magmatic melts.« less

Alkali trace elements in Gale crater, Mars, with ChemCam: Calibration update and geological implications

DOE PAGES

Payre, Valerie; Fabre, Cecile; Cousin, Agnes; ...

2017-03-20

The Chemistry Camera (ChemCam) instrument onboard Curiosity can detect minor and trace elements such as lithium, strontium, rubidium, and barium. Their abundances can provide some insights about Mars' magmatic history and sedimentary processes. We focus on developing new quantitative models for these elements by using a new laboratory database (more than 400 samples) that displays diverse compositions that are more relevant for Gale crater than the previous ChemCam database. These models are based on univariate calibration curves. For each element, the best model is selected depending on the results obtained by using the ChemCam calibration targets onboard Curiosity. New quantificationsmore » of Li, Sr, Rb, and Ba in Gale samples have been obtained for the first 1000 Martian days. Comparing these data in alkaline and magnesian rocks with the felsic and mafic clasts from the Martian meteorite NWA7533—from approximately the same geologic period—we observe a similar behavior: Sr, Rb, and Ba are more concentrated in soluble- and incompatible-element-rich mineral phases (Si, Al, and alkali-rich). Correlations between these trace elements and potassium in materials analyzed by ChemCam reveal a strong affinity with K-bearing phases such as feldspars, K-phyllosilicates, and potentially micas in igneous and sedimentary rocks. However, lithium is found in comparable abundances in alkali-rich and magnesium-rich Gale rocks. This very soluble element can be associated with both alkali and Mg-Fe phases such as pyroxene and feldspar. Here, these observations of Li, Sr, Rb, and Ba mineralogical associations highlight their substitution with potassium and their incompatibility in magmatic melts.« less

Role of Fluids in Lunar vs. Terrestrial Gabbros During Late-Stage and Post-Magmatic Crystallization, a Case Study

NASA Astrophysics Data System (ADS)

Fagan, T. J.; Fujimoto, A.; Kosaka, D.

2018-04-01

Incompatible elements, including H2O, are concentrated in late-stage magmatic pockets in gabbros from the Earth and Moon. Feldspar near the pockets is albitized by water (Earth case) or has discontinuous, unexplained changes in composition (Moon).

Kolmogorov proof of the Clauser, Horne, Shimony and Holt inequalities

NASA Astrophysics Data System (ADS)

Revzen, M.

Boolean logic is used to prove the CHSH inequalities. The proof elucidates the connection between Einstein elements of reality and quantum non-locality. The violation of the CHSH inequality by quantum theory is discussed and the two-stage view of quantum measurement relevance to incompatible observables is outlined.

Water in the Lunar Interior and the Apparent KREEP-Mare Dichotomy

NASA Astrophysics Data System (ADS)

McCubbin, F. M.; Nekvasil, H.

2010-12-01

Recent SIMS analysis of lunar apatite has shown that hydroxyl is structurally bound within lunar apatite from a number of different lunar lithologic types (McCubbin et al., 2010a, 2010b; Boyce et al., 2010; Greenwood et al., 2010). These studies along with previous SIMS analyses of lunar fire fountain glasses (Saal et al., 2008) confirm that there is at least some water in the lunar interior, with abundance estimates in magmatic source regions ranging from 64 ppb to 5 ppm water (McCubbin et al., 2010a). Surprisingly, apatite from rocks with KREEP-rich incompatible trace element signatures are depleted in hydroxyl in comparison to apatite from typical mare basalts. This result is counter-intuitive to the lunar magma ocean model, which predicts that incompatible constituents (e.g., water) would have been concentrated in the last dregs of liquid referred to as “urKREEP”. The mare basalts, which formed by partial melting of earlier LMO cumulates, are typically depleted in these incompatible constituents. Complicating the issue further, chlorine, another incompatible magmatic volatile element in apatite, follows the predicted trend with apatite from KREEP-rich rocks containing significant chlorine concentrations in comparison to apatite from mare basalts (McCubbin et al., 2009). The preceding results imply one of two scenarios 1) Water did not behave incompatibly during LMO crystallization and was preferentially stored within the LMO cumulate minerals 2) A secondary process such as degassing has perturbed the initial volatile contents of the urKREEP liquid or of the secondary magmas that have KREEP-rich incompatible trace element signatures. In regards to the first scenario, the mineral melt partition coefficients for water would need to have exceeded unity at the very low water concentrations of the LMO liquid. This scenario is consistent with the behavior of chlorine, as chlorine is not typically stored in nominally anhydrous phases like pyroxene or olivine, likely due to its large ionic radius. However, there is no empirical or experimental evidence to support the elevated D values for water. Regarding the second scenario, if significant degassing of the urKREEP liquid or KREEP-rich secondary magmas occurred, water would have certainly been lost preferentially to the other volatile constituents in apatite (fluorine and chlorine); however chlorine isotopes analyzed in lunar apatites are highly fractionated (Sharp et al., 2010), indicating degassing of chlorine in the absence of water. Therefore, this scenario only works if degassing on the Moon was a multi-stage and complex process where water and chlorine degassing are decoupled, which is not typically the case for terrestrial systems (Aiuppa et al., 2009, Webster and De Vivo, 2002; Webster et al., 1999). Solving this apparent KREEP-mare dichotomy regarding magmatic volatiles in the lunar interior is the next important step in figuring out the importance, relevance, and implications of water in the lunar interior. Moreover, it will lend insight into the roles of the other magmatic volatiles during the thermal and magmatic evolution of the Moon.

Specific down-regulation of spermatogenesis genes targeted by 22G RNAs in hybrid sterile males associated with an X-Chromosome introgression.

PubMed

Li, Runsheng; Ren, Xiaoliang; Bi, Yu; Ho, Vincy Wing Sze; Hsieh, Chia-Ling; Young, Amanda; Zhang, Zhihong; Lin, Tingting; Zhao, Yanmei; Miao, Long; Sarkies, Peter; Zhao, Zhongying

2016-09-01

Hybrid incompatibility (HI) prevents gene flow between species, thus lying at the heart of speciation genetics. One of the most common HIs is male sterility. Two superficially contradictory observations exist for hybrid male sterility. First, an introgression on the X Chromosome is more likely to produce male sterility than on autosome (so-called large-X theory); second, spermatogenesis genes are enriched on the autosomes but depleted on the X Chromosome (demasculinization of X Chromosome). Analysis of gene expression in Drosophila hybrids suggests a genetic interaction between the X Chromosome and autosomes that is essential for male fertility. However, the prevalence of such an interaction and its underlying mechanism remain largely unknown. Here we examine the interaction in nematode species by contrasting the expression of both coding genes and transposable elements (TEs) between hybrid sterile males and its parental nematode males. We use two lines of hybrid sterile males, each carrying an independent introgression fragment from Caenorhabditis briggsae X Chromosome in an otherwise Caenorhabditis nigoni background, which demonstrate similar defects in spermatogenesis. We observe a similar pattern of down-regulated genes that are specific for spermatogenesis between the two hybrids. Importantly, the down-regulated genes caused by the X Chromosome introgressions show a significant enrichment on the autosomes, supporting an epistatic interaction between the X Chromosome and autosomes. We investigate the underlying mechanism of the interaction by measuring small RNAs and find that a subset of 22G RNAs specifically targeting the down-regulated spermatogenesis genes is significantly up-regulated in hybrids, suggesting that perturbation of small RNA-mediated regulation may contribute to the X-autosome interaction. © 2016 Li et al.; Published by Cold Spring Harbor Laboratory Press.

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.

Enrichment Zoning Options for the Small Nuclear Rocket Engine (SNRE)

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

Bruce G. Schnitzler; Stanley K. Borowski

2010-07-01

Advancement of U.S. scientific, security, and economic interests through a robust space exploration program requires high performance propulsion systems to support a variety of robotic and crewed missions beyond low Earth orbit. In NASA’s recent Mars Design Reference Architecture (DRA) 5.0 study (NASA-SP-2009-566, July 2009), nuclear thermal propulsion (NTP) was again selected over chemical propulsion as the preferred in-space transportation system option because of its high thrust and high specific impulse (-900 s) capability, increased tolerance to payload mass growth and architecture changes, and lower total initial mass in low Earth orbit. An extensive nuclear thermal rocket technology development effortmore » was conducted from 1955-1973 under the Rover/NERVA Program. The Small Nuclear Rocket Engine (SNRE) was the last engine design studied by the Los Alamos National Laboratory during the program. At the time, this engine was a state-of-the-art design incorporating lessons learned from the very successful technology development program. Past activities at the NASA Glenn Research Center have included development of highly detailed MCNP Monte Carlo transport models of the SNRE and other small engine designs. Preliminary core configurations typically employ fuel elements with fixed fuel composition and fissile material enrichment. Uniform fuel loadings result in undesirable radial power and temperature profiles in the engines. Engine performance can be improved by some combination of propellant flow control at the fuel element level and by varying the fuel composition. Enrichment zoning at the fuel element level with lower enrichments in the higher power elements at the core center and on the core periphery is particularly effective. Power flattening by enrichment zoning typically results in more uniform propellant exit temperatures and improved engine performance. For the SNRE, element enrichment zoning provided very flat radial power profiles with 551 of the 564 fuel elements within 1% of the average element power. Results for this and alternate enrichment zoning options for the SNRE are compared.« less

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.

Mineral potential for incompatible element deposits hosted in pegmatites, alkaline rocks, and carbonatites in the Islamic Republic of Mauritania (phase V, deliverable 87): Chapter Q in Second projet de renforcement institutionnel du secteur minier de la République Islamique de Mauritanie (PRISM-II)

USGS Publications Warehouse

Taylor, Cliff D.; Giles, Stuart A.

2015-01-01

USGS review of PRISM-I data suggests that there is abundant documentation of the Bou Naga alkaline complex and to a lesser degree, the Guelb er Richat carbonatite complex, but that all other occurrences of U, Th, REE, and associated elements are poorly described, and poorly understood (Taylor, 2007)

A 1.5 Ma record of plume-ridge interaction at the Western Galápagos Spreading Center (91°40‧-92°00‧W)

NASA Astrophysics Data System (ADS)

Herbrich, Antje; Hauff, Folkmar; Hoernle, Kaj; Werner, Reinhard; Garbe-Schönberg, Dieter; White, Scott

2016-07-01

Shallow (elevated) portions of mid-ocean ridges with enriched geochemical compositions near hotspots document the interaction of hot, geochemically-enriched plume mantle with shallow depleted upper mantle. Whereas the spatial variations in geochemical composition of ocean crust along the ridge axis in areas where plume-ridge interaction is taking place have been studied globally, only restricted information exists concerning temporal variations in geochemistry of ocean crust formed through plume-ridge interaction. Here we present a detailed geochemical study of 0-1.5 Ma ocean crust sampled from the Western Galápagos Spreading Center (WGSC) axis to 50 km north of the axis, an area that is presently experiencing a high influx of mantle material from the Galápagos hotspot. The tholeiitic to basaltic andesitic fresh glass and few bulk rock samples have incompatible element abundances and Sr-Nd-Pb isotopic compositions intermediate between depleted normal mid-ocean-ridge basalt (N-MORB) from >95.5°W along the WGSC and enriched lavas from the Galápagos Archipelago, displaying enriched (E-)MORB type compositions. Only limited and no systematic geochemical variations are observed with distance from the ridge axis for <1.0 Ma old WGSC crust, whereas 1.0-1.5 Ma old crust trends to more enriched isotopic compositions in 87Sr/86Sr, 143Nd/144Nd, 207Pb/204Pb and 208Pb/204Pb isotope ratios. On isotope correlation diagrams, the data set displays correlations between depleted MORB and two enriched components. Neither the geographically referenced geochemical domains of the Galápagos Archipelago nor the end members used for principal component analysis can successfully describe the observed mixing relations. Notably an off-axis volcanic cone at site DR63 has the appropriate composition to serve as the enriched component for the younger WGSC and could represent a portion of the northern part of the Galápagos plume not sampled south of the WGSC. Similar compositions to samples from volcanic cone DR63 have been found in the northern part of the 11-14 Ma Galápagos hotspot track offshore Costa Rica, indicating that this composition is derived from the northern portion of the Galápagos plume. The older WGSC requires involvement of an enriched mantle two (EMII) type source, not recognized thus far in the Galápagos system, and is interpreted to reflect entrained material either from small-scale heterogeneities within the upper mantle or from the mantle transition zone. Overall the source material for the 0-1.5 Ma WGSC ocean crust appears to represent mixing of depleted upper mantle with Northern Galápagos Plume material of relatively uniform composition in relatively constant proportions.

Geochemical constraints on the petrogenesis of the pyroclastic rocks in Abakaliki basin (Lower Benue Rift), Southeastern Nigeria

NASA Astrophysics Data System (ADS)

Chukwu, Anthony; Obiora, Smart C.

2018-05-01

The pyroclastic rocks in the Cretaceous Abakaliki basin occur mostly as oval-shaped bodies, consisting of lithic/lava and vitric fragments. They are commonly characterized by parallel and cross laminations, as well contain xenoliths of shale, mudstone and siltstones from the older Asu River Group of Albian age. The rocks are basic to ultrabasic in composition, comprising altered alkali basalts, altered tuffs, minor lapillistones and agglomerates. The mineral compositions are characterized mainly by laths of calcic plagioclase, pyroxene (altered), altered olivines and opaques. Calcite, zeolite and quartz represent the secondary mineral constituents. Geochemically, two groups of volcaniclastic rocks, are distinguished: alkaline and tholeiitic rocks, both represented by fresh and altered rock samples. The older alkali basalts occur within the core of the Abakaliki anticlinorium while the younger tholeiites occur towards the periphery. Though most of the rocks are moderate to highly altered [Loss on ignition (LOI, 3.43-22.07 wt. %)], the use of immobile trace element such as Nb, Zr, Y, Hf, Ti, Ta and REEs reflect asthenospheric mantle source compositions. The rocks are enriched in incompatible elements and REEs (∑REE = 87.98-281.0 ppm for alkaline and 69.45-287.99 ppm for tholeiites). The ratios of La/Ybn are higher in the alkaline rocks ranging from 7.69 to 31.55 compared to the tholeiitic rocks which range from 4.4 to 16.89 and indicating the presence of garnet-bearing lherzolite in the source mantle. The spidergrams and REEs patterns along with Zr/Nb, Ba/Nb, Rb/Nb ratios suggest that the rocks were generated by a mantle plume from partial melting of mixed enriched mantle sources (HIMU, EMI and EMII) similar to the rocks of the south Atlantic Ocean such as St. Helena (alkaline rocks) and Ascension rocks (tholeiitic rocks). The rocks were formed in a within-plate setting of the intra-continental rift type similar to other igneous rocks in the Benue Rift and are not related to any subduction event as previously suggested.

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.

Hyperacid volcano-hydrothermal fluids from Copahue volcano, Argentina: Analogs for "subduction zone fluids"?

NASA Astrophysics Data System (ADS)

Varekamp, J. C.

2007-12-01

Hyperacid concentrated Chlorine-Sulfate brines occur in many young arc volcanoes, with pH values <1, high concentrations of volcanogenic elements (S, Cl, F, As, B) and the main rock forming elements (Ca, Al, Mg, K, Na, P). Sulfur isotope data and Silica thermometry from such fluids sampled over a ten year period from the Copahue volcanic system (Argentina) suggest reservoir temperatures of 175-300 oC, whereas the surface fluids do not exceed local boiling temperatures. These fluids are generated at much lower P-T conditions than fluids associated with a dehydrating subducted sediment complex below arc volcanoes, but their fundamental chemical compositions may have similarities. Incompatible trace element, major element concentrations and Pb isotope compositions of the fluids were used to determine the most likely rock protoliths for these fluids. Mean rock- normalized trace element diagrams then indicate which elements are quantitatively extracted from the rocks and which are left behind or precipitated in secondary phases. Most LILE show flat rock-normalized patterns, indicating close to congruent dissolution, whereas Ta-Nb-Ti show strong depletions in the rock-normalized diagrams. These HFSE are either left behind in the altered rock protolith or were precipitated along the way up. The behavior of U and Th is almost identical, suggesting that in these low pH fluids with abundant ligands Th is just as easily transported as U, which is not the case in more dilute, neutral fluids. Most analyzed fluids have steeper LREE patterns than the rocks and have negative Eu anomalies similar to the rocks. Fluids that interacted with newly intruded magma e.g., during the 2000 eruption, have much less pronounced Eu anomalies, which was most likely caused by the preferential dissolution of plagioclase when newly intruded magma interacted with the acid fluids. The fluids show a strong positive correlation between Y and Cd (similar to MORB basalts, Yi et al., JGR, 2000), suggesting that Cd is mainly a rock-derived element that may not show chalcophilic behavior. The fluids are strongly enriched (relative to rock) in As, Zn and Pb, suggesting that these elements were carried with the volcanic gas phase into the system. In summary, if these fluids are broadly similar to fluids from dehydrating subducted sediments, they tend to transport preferently the LILE, LREE, U as well as Th, while the HFSE are left behind.

Method for laser induced isotope enrichment

DOEpatents

Pronko, Peter P.; Vanrompay, Paul A.; Zhang, Zhiyu

2004-09-07

Methods for separating isotopes or chemical species of an element and causing enrichment of a desired isotope or chemical species of an element utilizing laser ablation plasmas to modify or fabricate a material containing such isotopes or chemical species are provided. This invention may be used for a wide variety of materials which contain elements having different isotopes or chemical species.

The monzonorite-anorthosite connection: The petrogenesis of terrestrial KREEP

NASA Technical Reports Server (NTRS)

Longhi, J.; Auwera, J. Vander

1993-01-01

There is a suite of rocks typically associated with Proterozoic massif anorthosites that bear some interesting similarities to lunar KREEP. In many cases these rocks are plutonic and have traditionally been referred to as the jotunite-mangerite-+/-charnockite-+/-syenite suite. However, in the Rogaland district of southwestern Norway, where they are referred to as 'monzonorites', these rocks are also present as fine-grained dikes and as the chill margin of a layered intrusion, and thus approximate magmatic liquid compositions are readily obtained by chemical analysis. Monzonorites are typically enriched in incompatible lithophile elements such as K (alkali feldspar is present), the rare earths (REE), and P. They have intermediate to low Mg', low-Ca pyroxene, and more evolved types have low Ti/Sm ratios. Much debate has developed over attempts to explain the link between monzonorites and massif anorthosites. One feature seems clear: monzonorites and associated anorthosites have different initial isotopic ratios, so a simple relation is not possible. However, there is apparently a continuum in major elements between the monzonorites and gabbros believed to represent magmas parental to the anorthosites. This continuum suggests a link via high pressure fractionation coupled with assimilation. Although more complicated, this scenario is similar to that evoked for the early Moon: following the formation of ferroan anorthosites, continued fractional crystallization of the residual liquids at the base of the crust led to the formation of KREEP. An attempt is made here to establish a link between monzonorites and high-Al gabbros which are nearly always found as ancillary intrusions associated with anorthosites, and which may record processes in lower crustal magma chambers.

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.

K-Rich Basaltic Sources beneath Ultraslow Spreading Central Lena Trough in the Arctic Ocean

NASA Astrophysics Data System (ADS)

Ling, X.; Snow, J. E.; Li, Y.

2016-12-01

Magma sources fundamentally influence accretion processes at ultraslow spreading ridges. Potassium enriched Mid-Ocean Ridge Basalt (K-MORB) was dredged from the central Lena Trough (CLT) in the Arctic Ocean (Nauret et al., 2011). Its geochemical signatures indicate a heterogeneous mantle source with probable garnet present under low pressure. To explore the basaltic mantle sources beneath the study area, multiple models are carried out predicting melting sources and melting P-T conditions in this study. P-T conditions are estimated by the experimental derived thermobarometer from Hoang and Flower (1998). Batch melting model and major element model (AlphaMELTs) are used to calculate the heterogeneous mantle sources. The modeling suggests phlogopite is the dominant H2O-K bearing mineral in the magma source. 5% partial melting of phlogopite and amphibole mixing with depleted mantle (DM) melt is consistent with the incompatible element pattern of CLT basalt. P-T estimation shows 1198-1212oC/4-7kbar as the possible melting condition for CLT basalt. Whereas the chemical composition of north Lena Trough (NLT) basalt is similar to N-MORB, and the P-T estimation corresponds to 1300oC normal mantle adiabat. The CLT basalt bulk composition is of mixture of 40% of the K-MORB endmember and an N-MORB-like endmember similar to NLT basalt. Therefore the binary mixing of the two endmembers exists in the CLT region. This kind of mixing infers to the tectonic evolution of the region, which is simultaneous to the Arctic Ocean opening.

Microstructural and Compositional Relations of Granitoid Clasts in Lunar Breccias at the Micrometer to Sub-Micrometer Scale

NASA Technical Reports Server (NTRS)

Christoffersen, R.; Simon, J. I.; Mills, R. D.; Ross, D. K.; Tappa, M.

2015-01-01

Lunar granitoid lithologies have long been of interest for the information they provide on processes leading to silicic melt compositions on the Moon. The extraction of such melts over time affects the distribution and budget of incompatible materials (i.e., radiogenic heat producing elements and volatiles) of the lunar interior. We have recently shown that in addition to their high concentrations of incompatible lithophile elements, some granitoid clasts in lunar breccias have significant indigenous water contents in their alkali feldspars. This raises the importance of lunar granitoid materials in the expanding search for mineralogic/petrologic hosts of indigenous lunar water-related species. We are undertaking a detailed survey of the petrologic/mineralogical relations of granitoid clasts in lunar breccias to achieve a better understanding of the potential of these diverse assemblages as hosts for volatiles, and as candidates for additional isotope chronology studies. Our preliminary results reported here based on high-resolution field-emission SEM, EPMA and TEM studies uncover immense complexity in these materials at the micrometer to sub-micrometer scale that heretofore have not been fully documented.

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.

Crystallization and Melt Removal at Arenal Volcano, Polytopic Vector Analysis

NASA Astrophysics Data System (ADS)

Hidalgo, P. J.; Vogel, T. A.; Bolge, L. L.; Ehrlich, R.; Alvarado, G. E.

2007-12-01

Tephra sequences ET3 and ET4 from Arenal volcano in Costa Rica have recently been interpreted to be a product of crystal fractionation by Bolge and coworkers in a series of papers (2004, 2006). The two tephra units are part of a sequence of 22 tephra units that represent a 7000 year span of the Arenal volcano activity. The tephro- stratigraphy has been described extensively by Melson (1982; 1994). The ET3 and ET4 tephras were interpreted (based on major- and trace-element, isotopic analyses of whole rocks and microchemical analyses of individual phases) as clear evidence of crystal separation by gravity settling (Bolge et al., 2004, 2006). The lower ET4 tephra sequence (andesitic and crystal poor) and the upper ET3 tephra (basaltic and crystal rich) represent an inverted snapshot of the magma chamber with contrasting geochemical properties. The ET3 sequence (deeper part of the magma chamber) has nearly constant composition with only a few elements varying stratigraphically (best represented by CaO). This is consistent with gradually decreasing amounts of melt in the upper part of ET3. The lower ET4 tephra (upper part of the magma chamber) contains large chemical gradients in both incompatible and compatible elements. In the present study we use whole-rock geochemical data from the recent tephra sequences ET3 and ET4 as inputs to Polytopic Vector Analysis (PVA) (for a review of this method see Vogel and coworkers, in press). With this method we produce a three end member solution that is consistent with crystallization of Olivine, plagioclase and pyroxene from the most mafic end member (EM1) resulting in a crystal rich mush zone. As crystallization progresses the compositions of the liquids are driven towards an intermediate end member (EM3), which has an intermediate composition liquid. At EM3 composition, rapid depletion of FeO, MgO and TiO2 by crystallization of Fe-Ti oxides, rapidly drives the liquid composition towards the silicic EM1 (incompatible element enriched end member). Using PVA we refine the interpretations of Bolge and coworkers and show that melt from the crystalline rich ET3 tephra was removed and ponded in the magma chamber above the crystalline mush (top part of ET4 unit). Thus when the eruption occurred the most evolved tephra (ET4) were deposited first followed by the least evolved tephra (ET3), which resulted in sampling of a chemically zoned magma chamber. Using PVA on stratigraphically controlled whole-rock analyses of tephra samples, we can unambiguously identify processes and end members that are involved in crystal accumulation and liquid separation processes. Thus PVA is a rigorous analytical tool that uses only whole-rock chemical data to produce robust results that can be used with other analytical techniques to test petrological models.

Production and recycling of oceanic crust in the early Earth

NASA Astrophysics Data System (ADS)

van Thienen, P.; van den Berg, A. P.; Vlaar, N. J.

2004-08-01

Because of the strongly different conditions in the mantle of the early Earth regarding temperature and viscosity, present-day geodynamics cannot simply be extrapolated back to the early history of the Earth. We use numerical thermochemical convection models including partial melting and a simple mechanism for melt segregation and oceanic crust production to investigate an alternative suite of dynamics which may have been in operation in the early Earth. Our modelling results show three processes that may have played an important role in the production and recycling of oceanic crust: (1) Small-scale ( x×100 km) convection involving the lower crust and shallow upper mantle. Partial melting and thus crustal production takes place in the upwelling limb and delamination of the eclogitic lower crust in the downwelling limb. (2) Large-scale resurfacing events in which (nearly) the complete crust sinks into the (eventually lower) mantle, thereby forming a stable reservoir enriched in incompatible elements in the deep mantle. New crust is simultaneously formed at the surface from segregating melt. (3) Intrusion of lower mantle diapirs with a high excess temperature (about 250 K) into the upper mantle, causing massive melting and crustal growth. This allows for plumes in the Archean upper mantle with a much higher excess temperature than previously expected from theoretical considerations.

Searching for neuKREEP: An EMP study of Apollo 11 Group A basalts

NASA Technical Reports Server (NTRS)

Jerde, Eric A.; Taylor, Lawrence A.

1993-01-01

The Apollo 11 and 17 landing sites are characterized by the presence of high-Ti basalts (TiO2 greater than 6 percent). The Group A basalts of Apollo 11 have elevated K compositions (greater than 2000 ppm); and are enriched in incompatible trace elements relative to the other types of high-Ti basalt found in the region. These unique basalts also are the youngest of all high-Ti basalts, with an age of 3.56 +/- 0.02 Ga. Recent modelling of the Apollo 11 Group A basalts by Jerde et al. has demonstrated that this unique variety of high-Ti basalt may have formed through fractionation of a liquid with the composition of the Apollo 11 orange glass, coupled with assimilation of evolved material (dubbed neuKREEP and having similarities to lunar quartz monzodiorite). Assimilation of this material would impart its REE signature on the liquid, resulting in the elevated REE abundances observed. Minerals such as whitlockite which contain a large portion of the REE budget can be expected to reflect the REE characteristics of the assimilant. To this end, an examination of the whitlockite present in the Apollo 11 Group A basalts was undertaken to search for evidence of the neuKREEP material assimilated.

Is It Now Institutionally Appropriate for the Courts to Consider Whether the Assisted Dying Ban is Human Rights Compatible? Conway V Secretary of State for Justice.

PubMed

Hobson, Clark

2017-11-07

Noel Conway has ultimately been granted permission to apply for judicial review, to seek a declaration under section 4(2) Human Rights Act 1998 that section 2(1) Suicide Act 1961 is incompatible with his right to respect for private life under Article 8(1) ECHR. Both decisions in the application process are significant. They attempt to deal with the qualitative elements in the reasoning of Lords Neuberger, Mance and Wilson, in Nicklinson v Ministry of Justice: what Parliament is required to have done to have 'satisfactorily addressed' the question of relaxing or modifying section 2(1) Suicide Act. In failing to consider the explicit use of qualitative reasoning, both courts fail to interpret Nicklinson properly-that Parliament must change the law, with a declaration of incompatibility likely if it failed to do so. The Court of Appeal was correct to overrule the High Court's unqualified approach to whether it was now institutionally appropriate for a court to consider issuing a declaration of incompatibility, for the purposes of granting permission to apply for judicial review. However, the Court of Appeal directly signals their belief that a range of primary evidence bears out a system of assisted suicide for those in Mr Conway's position could feasibly be devised. This question though, as to evidence of a feasible system in the future, is irrelevant to whether permission to apply for judicial review should be granted to argue it is institutionally appropriate to make a declaration of incompatibility regarding current legislation. This is a problem Nicklinson has made for assisted dying and incompatibility debates. © The Author 2017. Published by Oxford University Press; all rights reserved. For Permissions, please email: journals.permissions@oup.com.

St Paul fracture zone intratransform ridge basalts (Equatorial Atlantic): Insight within the mantle source diversity

NASA Astrophysics Data System (ADS)

Hemond, C.; Brunelli, D.; Maia, M.; Prigent, S.; Sichel, S. E.

2017-12-01

The St Paul Transform System offsets by 630 km the Equatorial Mid Atlantic Ridge at 1° N. It consists of four Major faults separating three intra transform ridge axes. Volcanic glassy samples were collected inside two intratransform ridge (ITR) segments during the COLMEIA cruise (Maia et al ; 2016) and samples from the third ITR available from a previous cruise ST PAUL (Hékinian et al. 2000). Major, trace elements and Hf, Pb, Sr and Nd isotopes were determined on selected hand picked glass chips. Few glassy samples recovered and analysed from abyssal hill samples open a time window of about 4.5 million years in the chemistry of the northern ITR. Results show that all samples are basaltic in composition but trace elements display contrasting images for the three ITR. The northern ITR samples are all light REE and highly incompatible enriched and are E-MORB; the central ITR samples display rather flat REE pattern with a level on enrichment of the HREE higher than the other two ITR and are T-MORB. Southern ITR samples are more heterogeneous N-MORB to T-MORB with a lower level of HREE. Isotopes reveal that the ITRs sample distinct mantle sources. In various isotope plans, the northern ITR samples plot together with published results from the MAR directly north of the St Paul F.Z. Therefore they exhibit some flavor of the Sierra Leone hotspot interacting with the MAR at 1.7°N. Central and southern ITR samples have very distinct composition from the northern ITR but resemble each other. However, for identical 206Pb/204Pb ratios, central ITR has slightly but significantly higher 207Pb/204Pb and 208Pb/204Pb, also higher 143Nd/144Nd for a given 87Sr/86Sr. Southern ITR is in chemical continuity of the MAR southward. So that central ITR samples display a rather specific composition. Off axis samples corresponding to the activity of the northern ITR up to 4.6 m.y. show that the hotspot contribution was even bigger on the spreading axis than today and might be fading with time as the MAR gets away from the Hotspot. It remains to explain how the flow of enriched material derived from the Sierra Leone hotspot passed through the large transform fault that limits the St Paul zone to the north. It is also of interest to explain the peculiar compositions of the central ITR samples that reflect neither the northern adjacent MAR composition nor the southern one.

Pliocene to late Pleistocene magmatism in the Aurora Volcanic Field, Nevada and California, USA

NASA Astrophysics Data System (ADS)

Kingdon, S.; Cousens, B.; John, D. A.; du Bray, E. A.

2013-12-01

The 3.9- 0.1 Ma Aurora Volcanic Field (AVF) covers 325 km2 east and southeast of the Bodie Hills, north of Mono Lake, California, USA. The AVF is located immediately northwest of the Long Valley magmatic system and adjacent and overlapping the Miocene Bodie Hills Volcanic Field (BHVF). Rock types range from trachybasalt to trachydacite, and high-silica rhyolite. The trachybasalts to trachydacites are weakly to moderately porphyritic (1-30%) with variable phenocryst assemblages that are some combination of plagioclase, hornblende, clinopyroxene, and lesser orthopyroxene, olivine, and/or biotite. Microphenocrysts are dominated by plagioclase, and include opaque oxides, clinopyroxene, and apatite. These rocks are weakly to strongly devitrified. The high-silica rhyolites are sparsely porphyritic with trace to 10% phenocrysts of quartz, sanidine, plagioclase, biotite, (+/- hornblende), accessory opaque oxide minerals, titanite, allanite, (+/-apatite, zircon), and have glassy groundmasses. Rocks in the AVF are less strongly porphyritic than those of BHVF. Plagioclase phenocrysts are often oscillatory zoned and many have sieve texture. Amphiboles have distinct black opaque rims. Xenocrystic quartz and plagioclase are rare. AVF lavas have bimodal SiO2 compositions, ranging from 49 to 78 wt%, with a gap between 65 and 75 wt%. They are high-K calc-alkaline to shoshonitic in composition, and are metaluminous to weakly peraluminous. They are enriched in rare earth elements (REE), especially light REEs, compared to the Miocene BHVF rocks. Primordial mantle-normalized incompatible element patterns show arc- or subduction-related signatures, with enrichment in Ba and Pb, and depletion in Nb and Ta. Enrichment in K and Sr and depletion in Ti are less pronounced than in the BHVF rocks. There is no correlation between lead isotope ratios and silica (initial 206Pb/204Pb ratios range from 18.974 to 19.151). Neodymium isotope ratios show a moderate negative correlation with silica within the range of 50 to 75 wt% SiO2 (initial 143Nd/144Nd ratios range from 0.51238 to 0.51258, and ɛNdt ranges from -1.09 to -4.01). Strontium ratios show a strong positive correlation with silica for SiO2 above 50 wt% (initial 87Sr/86Sr ratios range from 0.70513 to 0.70691). Pb, Nd, and Sr isotope compositions do not systematically change with time. The Aurora volcanic rocks are interpreted to be postsubduction erupted from an extensional tectonic setting. Compared with the BHVF rocks, the AVF rocks are more radiogenic and crustal assimilation is a more influential process.

Postglacial eruptive history of the Western Volcanic Zone, Iceland

NASA Astrophysics Data System (ADS)

Sinton, John; GröNvold, Karl; SæMundsson, KristjáN.

2005-12-01

New field observations, age constraints, and extensive chemical analyses define the complete postglacial eruptive history of the 170-km-long Western Volcanic Zone (WVZ) of Iceland, the ultraslow-spreading western boundary of the south Iceland microplate. We have identified 44 separate eruptive units, 10 of which are small-volume eruptions associated with the flanking Grímsnes system. Overall chemical variations are consistent with very simplified models of melting of a source approximating primitive mantle composition. The 17 eruptions in the first 3000 years of postglacial time account for about 64% of the total postglacial production and are incompatible-element depleted compared to younger units, consistent with enhanced melting as a consequence of rebound immediately following deglaciation. Steadily declining eruption rates for the last 9000 years also correlate with changes in average incompatible element ratios that appear to reflect continued decline in melting extents to the present day. This result is not restricted to the WVZ, however, and may herald a decline in melting throughout all of western Iceland during later postglacial time. Lavas from the northern part of the WVZ are depleted in incompatible elements relative to those farther south at all times, indicating either a long-wavelength gradient in mantle source composition or variations in the melting process along axis. We find no evidence in the postglacial volcanic record for current failure of the WVZ, despite evidence for continued propagation of the eastern margin of the microplate. The dominance of lava shields in the eruptive history of the WVZ contrasts with the higher number of fissure eruptions in other Icelandic volcanic zones. WVZ shields represent long-duration, low-effusion rate eruptions fed by recharge magma arising out of the mantle. Average effusion rate is the key variable distinguishing shield and fissure eruptions, both within the WVZ and between different volcanic zones. High effusion rate, large-volume eruptions require the presence of large crustal magma reservoirs, which have been rare or absent in the WVZ throughout postglacial time.

Chemical consequences of compaction within the freezing front of a crystallizing magma ocean

NASA Astrophysics Data System (ADS)

Hier-Majumder, S.; Hirschmann, M. M.

2013-12-01

The thermal and compositional evolution of planetary magma oceans have profound influences on the early development and differentiation of terrestrial planets. During crystallization, rejection of elements incompatible in precipitating solids leads to petrologic and geochemical planetary differentiation, including potentially development of a compositionally stratified early mantle and evolution of thick overlying atmospheres. In cases of extremely efficient segregation of melt and crystals, solidified early mantles can be nearly devoid of key incompatible species including heat-producing (U, Th, K) and volatile (H,C,N,& noble gas) elements. A key structural component of a crystallizing magma ocean is the partially molten freezing front. The dynamics of this region influences the distribution of incompatible elements between the earliest mantle and the initial surficial reservoirs. It also can be the locus of heating owing to the dissipation of large amounts of tidal energy potentially available from the early Moon. The dynamics are influenced by the solidification rate, which is coupled to the liberation of volatiles owing to the modulating greenhouse effects in the overlying thick atmosphere. Compaction and melt retention in the freezing front of a magma ocean has received little previous attention. While the front advances during the course of crystallization, coupled conservation of mass, momentum, and energy within the front controls distribution and retention of melt within this layer. Due to compaction within this layer, melt distribution is far from uniform, and the fraction of melt trapped within this front depends on the rate of freezing of the magma ocean. During phases of rapid freezing, high amount of trapped melt within the freezing front retains a larger quantity of dissolved volatiles and the reverse is true during slow periods of crystallization. Similar effects are known from inferred trapped liquid fractions in layered mafic intrusions. Here we develop a simple 1-D model of melt retention in the freezing front of a crystallizing magma ocean, and apply it to the thermal and chemical evolution of the early Earth.

Enrichment and distribution of 24 elements within the sub-sieve particle size distribution ranges of fly ash from wastes incinerator plants.

PubMed

Raclavská, Helena; Corsaro, Agnieszka; Hartmann-Koval, Silvie; Juchelková, Dagmar

2017-12-01

The management of an increasing amount of municipal waste via incineration has been gaining traction. Fly ash as a by-product of incineration of municipal solid waste is considered a hazardous waste due to the elevated content of various elements. The enrichment and distribution of 24 elements in fly ash from three wastes incinerators were evaluated. Two coarse (>100 μm and <100 μm) and five sub-sieve (12-16, 16-23, 23-34, 34-49, and 49-100 μm) particle size fractions separated on a cyclosizer system were analyzed. An enhancement in the enrichment factor was observed in all samples for the majority of elements in >100 μm range compared with <100 μm range. The enrichment factor of individual elements varied considerably within the samples as well as the sub-sieve particle size ranges. These variations were attributed primarily to: (i) the vaporization and condensation mechanisms, (ii) the different design of incineration plants, (iii) incineration properties, (iv) the type of material being incinerated, and (v) the affinity of elements. Copyright © 2017 Elsevier Ltd. All rights reserved.

Eruptive history and petrology of Mount Drum volcano, Wrangell Mountains, Alaska

USGS Publications Warehouse

Richter, D.H.; Moll-Stalcup, E. J.; Miller, T.P.; Lanphere, M.A.; Dalrymple, G.B.; Smith, R.L.

1994-01-01

Mount Drum is one of the youngest volcanoes in the subduction-related Wrangell volcanic field (80x200 km) of southcentral Alaska. It lies at the northwest end of a series of large, andesite-dominated shield volcanoes that show a northwesterly progression of age from 26 Ma near the Alaska-Yukon border to about 0.2 Ma at Mount Drum. The volcano was constructed between 750 and 250 ka during at least two cycles of cone building and ring-dome emplacement and was partially destroyed by violent explosive activity probably after 250 ka. Cone lavas range from basaltic andesite to dacite in composition; ring-domes are dacite to rhyolite. The last constructional activity occured in the vicinity of Snider Peak, on the south flank of the volcano, where extensive dacite flows and a dacite dome erupted at about 250 ka. The climactic explosive eruption, that destroyed the top and a part of the south flank of the volcano, produced more than 7 km3 of proximal hot and cold avalanche deposits and distal mudflows. The Mount Drum rocks have medium-K, calc-alkaline affinities and are generally plagioclase phyric. Silica contents range from 55.8 to 74.0 wt%, with a compositional gap between 66.8 and 72.8 wt%. All the rocks are enriched in alkali elements and depleted in Ta relative to the LREE, typical of volcanic arc rocks, but have higher MgO contents at a given SiO2, than typical orogenic medium-K andesites. Strontium-isotope ratios vary from 0.70292 to 0.70353. The compositional range of Mount Drum lavas is best explained by a combination of diverse parental magmas, magma mixing, and fractionation. The small, but significant, range in 87Sr/86Sr ratios in the basaltic andesites and the wide range of incompatible-element ratios exhibited by the basaltic andesites and andesites suggests the presence of compositionally diverse parent magmas. The lavas show abundant petrographic evidence of magma mixing, such as bimodal phenocryst size, resorbed phenocrysts, reaction rims, and disequilibrium mineral assemblages. In addition, some dacites and andesites contain Mg and Ni-rich olivines and/or have high MgO, Cr, Ni, Co, and Sc contents that are not in equilibrium with the host rock and indicate mixing between basalt or cumulate material and more evolved magmas. Incompatible element variations suggest that fractionation is responsible for some of the compositional range between basaltic andesite and dacite, but the rhyolites have K, Ba, Th, and Rb contents that are too low for the magmas to be generated by fractionation of the intermediate rocks. Limited Sr-isotope data support the possibility that the rhyolites may be partial melts of underlying volcanic rocks. ?? 1994 Springer-Verlag.

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.

Environmental Characteristics of Carbonatite and Alkaline Intrusion-related Rare Earth Element (REE) Deposits

NASA Astrophysics Data System (ADS)

Seal, R. R., II; Piatak, N. M.

2017-12-01

Carbonatites and alkaline intrusions are important sources of REEs. Environmental risks related to these deposit types have been assessed through literature review and evaluation of the geochemical properties of representative samples of mill tailings and their leachates. The main ore mineral in carbonatite deposits is bastnasite [(Ce,La)(CO3)F], which is found with dolomite and calcite ( 65 %), barite (20 - 25 %), plus a number of minor accessory minerals including sulfides such as galena and pyrite. Generally, alkaline intrusion-related REE deposits either occur in layered complexes or with dikes and veins cutting alkaline intrusions. Such intrusions have a more diverse group of REE ore minerals that include fluorcarbonates, oxides, silicates, and phosphates. Ore also can include minor calcite and iron (Fe), lead (Pb), and zinc (Zn) sulfides. The acid-generating potential of both deposit types is low because of a predominance of carbonate minerals in the carbonatite deposits, the presence of feldspars and minor calcite in alkaline intrusion-related deposits, and to only minor to trace occurrence of potentially acid-generating sulfide minerals. Both deposit types, however, are produced by igneous and hydrothermal processes that enrich high-field strength, incompatible elements, which typically are excluded from common rock-forming minerals. Elements such as yttrium (Y), niobium Nb), zirconium (Zr), hafnium (Hf), tungsten (W), titanium (Ti), tantalum (Ta), scandium (Sc), thorium (Th), and uranium (U) can be characteristic of these deposits and may be of environmental concern. Most of these elements, including the REEs, but with the exception of U, have low solubilities in water at the near-neutral pH values expected around these deposits. Mill tailings from carbonatite deposits can exceed residential soil and sediment criteria for Pb, and leachates from mill tailings can exceed drinking water guidelines for Pb. The greatest environmental challenges, however, are linked to the presence of Th and U, although mineral hosts for these elements are moderately unreactive in the environment. Both deposit types can have mill tailings that exceed residential soil criteria for U. Uranium can be recovered as a byproduct to mitigate its environmental effects, but Th remains a waste product that requires management.

Multiple Sulfur Isotopes In The Molopo Farms Complex May Shed Light On Mechanisms Of Mineralization In The Bushveld Igneous Complex

NASA Astrophysics Data System (ADS)

Magalhaes, N.; Feineman, M. D.; Bybee, G. M.; Penniston-Dorland, S.; Farquhar, J.; Draper, C.; Escobar, E.; Gates, M.; Renusch, J.

2016-12-01

The 2.056 Ga Bushveld Igneous Complex (BIC) is host to the world's largest layered mafic-ultramafic intrusion, the Rustenburg Layered Suite (RLS), which has >80% of the world's known platinum group elements (PGEs) reserves. The BIC results from large-volume melt extraction from the mantle and may provide insight into the formation and compositional evolution of continental crust. Despite its scientific and economic importance, the total magma volume is poorly known. This is in part because the relationship between the BIC and nearby intrusive bodies of similar age remains uncertain. In this study, we present major element, trace element, and multiple sulfur isotope data for a suite of samples spanning the stratigraphy of the Molopo Farms Complex (MFC), a layered mafic intrusion located 200 km west of the Far Western Limb of the RLS. Similar to the RLS, the MFC contains an ultramafic lower zone, a mafic main zone, and an incompatible element enriched granophyric unit near the contact with the roof rocks. However, it has no Critical Zone, and an insignificant concentration of PGEs. Since the PGEs in the RLS are primarily hosted in sulfides, it has been inferred that the mineralization is closely linked to the source and behavior of sulfur. The RLS displays mass independent fractionation of sulfur (S-MIF; denoted by Δ33S), which suggests incorporation of surface-derived materials into the magma prior to or during emplacement. Multiple sulfur isotopes of MFC samples also show non-zero mean Δ33S (0.04±0.02‰, 1sd), although it is lower than the mean for the RLS (0.11±0.02‰, 1sd). Similarities in trace element ratios between the MFC mafic zone and RLS marginal zone suggest the same parental magma contributed to both intrusions. Taken together, these results suggest that both the RLS and the MFC started with similar magmatic compositions, and while both assimilated sulfur with an Archean surface-derived component, the RLS received more of this component in proportion to its volume. The lack of PGE mineralization in the MFC may reflect the lesser addition of Archean sedimentary sulfur.

Volcanic and anthropogenic contribution to heavy metal content in lichens from Mt. Etna and Vulcano island (Sicily).

PubMed

Varrica, D; Aiuppa, A; Dongarrà, G

2000-05-01

Major and trace element concentrations were determined in two lichen species (Parmelia conspersa and Xanthoria calcicola) from the island of Vulcano and all around Mt. Etna. In both areas, the average concentrations of Al, Ca, Mg, Fe, Na, K, P and Ti are substantially greater than those of other elements. Several elements (Br, Pb, Sb, Au, Zn, Cu) resulted enriched with respect to the local substrates. The Br and Pb enrichment factors turned out to be the highest among those calculated in both areas. Data indicate that mixing between volcanic and automotive-produced particles clearly explains the range of Pb/Br shown by lichen samples. Sb is also enriched, revealing a geogenic origin at Vulcano and a prevailing anthropic origin at Mt. Etna. Distribution maps of the enrichment factors show a generalized enrichment of Au and Zn near Mt. Etna, whereas Cu appears to be enriched prevalently in the NE-SE area. The highest levels of Au and Cu at Vulcano occur E-SE from the craters, following the prevailing wind direction.

Microalloying of transition metal silicides by mechanical activation and field-activated reaction

DOEpatents

Munir, Zuhair A [Davis, CA; Woolman, Joseph N [Davis, CA; Petrovic, John J [Los Alamos, NM

2003-09-02

Alloys of transition metal suicides that contain one or more alloying elements are fabricated by a two-stage process involving mechanical activation as the first stage and densification and field-activated reaction as the second stage. Mechanical activation, preferably performed by high-energy planetary milling, results in the incorporation of atoms of the alloying element(s) into the crystal lattice of the transition metal, while the densification and field-activated reaction, preferably performed by spark plasma sintering, result in the formation of the alloyed transition metal silicide. Among the many advantages of the process are its ability to accommodate materials that are incompatible in other alloying methods.

The petrogenesis of L-6 chondrites - Insights from the chemistry of minerals

NASA Technical Reports Server (NTRS)

Curtis, D. B.; Schmitt, R. A.

1979-01-01

Measurements of the major, minor and trace element abundances of the major minerals of the L-6 chondrites Alfianello, Colby (WI) and Leedey are used to investigate the formation mechanisms of L-6 chondrites. Electron microprobe analysis was performed on individual grains of each mineral, and separated minerals were analyzed by instrumental and radiochemical neutron activation analysis. The compositions of the three meteorites are observed to be generally uniform, however different abundances and distributions of rare earth elements and Co and Ni indicate that the meteorites have different petrogenetic histories. Alkali element distributions are found to be incompatible with internal equilibration of a closed system.

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

NASA Astrophysics Data System (ADS)

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

1997-08-01

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

The influence of carbon, sulfur, and silicon on trace element partitioning in iron alloys

NASA Astrophysics Data System (ADS)

Han, J.; Van Orman, J. A.; Crispin, K. L.; Ash, R. D.

2014-12-01

Non-metallic light elements are important constituents of planetary cores and have a strong influence on the partitioning behavior of trace elements. Planetary cores may contain a wide range of non-metallic light elements, including H, N, S, P, Si, and C. Under highly reducing conditions, such as those that are thought to have pertained during the formation of Mercury's core, Si and C, in addition to sulfur, may be particularly important constituents. Each of these elements may strongly effect and have a different impact on the partitioning behavior of trace elements but their combined effects on trace element partitioning have not been quantified. We investigated the partitioning behavior of more than 25 siderophile trace elements within the Fe-S-C-Si system with varying concentrations of C, S, and Si. The experiments were performed under pressures varying from 1 atm to 2 GPa and temperatures ranging from 1200˚C to 1450˚C. All experiments produced immiscible liquids, one enriched in Si and C, and the other predominantly FeS. We found some highly siderophile elements including Os, Ru, Ir, and Re are much more enriched in Fe-Si-C phase than in Fe-S phase, whereas other trace elements like V, Co, Ag, Hf, and Pb are enriched in S-rich phase. However, not all the trace elements enriched in Fe-Si-C phase are repelled by sulfur. Elements like Re and Ru could have different partitioning trends if sulfur concentration in S-rich phase rises. The partitioning behavior of these trace elements could enhance our understanding of the differentiation of Mercury's core under oxygen-poor conditions.

Germanium abundances in lunar basalts: Evidence of mantle metasomatism

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

Dickinson, T.; Taylor, G.J.; Keil, T.K.

1988-01-01

To fill in gaps in the present Ge data base, mare basalts were analyzed for Ge and other elements by RNAA and INAA. Mare basalts from Apollo 11, 12, 15, 17 landing sites are rather uniform in Ge abundance, but Apollo 14 aluminous mare basalts and KREEP are enriched in Ge by factors of up to 300 compared to typical mare basalts. These Ge enrichments are not associated with other siderophile element enrichments and, thus, are not due to differences in the amount of metal segregated during core formation. Based on crystal-chemical and inter-element variations, it does not appear thatmore » the observed Ge enrichments are due to silicate liquid immiscibility. Elemental ratios in Apollo 14 aluminous mare basalts, green and orange glass, average basalts and KREEP suggest that incorporation of late accreting material into the source regions or interaction of the magmas with primitive undifferentiated material is not a likely cause for the observed Ge enrichments. We speculate that the most plausible explanation for these Ge enrichments is complexing and concentration of Ge by F, Cl or S in volatile phases. In this manner, the KREEP basalt source regions may have been metasomatized and Apollo 14 aluminous mare basalt magmas may have become enriched in Ge by interacting with these metasomatized areas. The presence of volatile- and Ge-rich regions in the Moon suggests that the Moon was never totally molten. 71 refs., 1 fig., 6 tabs.« less

A baseline record of trace elements concentration along the beach placer mining areas of Kanyakumari coast, South India.

PubMed

Simon Peter, T; Chandrasekar, N; John Wilson, J S; Selvakumar, S; Krishnakumar, S; Magesh, N S

2017-06-15

Trace element concentration in the beach placer mining areas of Kanyakumari coast, South India was assessed. Sewage and contaminated sediments from mining sites has contaminated the surface sediments. Enrichment factor indicates moderately severe enrichment for Pb, minor enrichment for Mn, Zn, Ni, Fe and no enrichment for Cr and Cu. The Igeo values show higher concentration of Pb ranging in the scale of 3-4, which shows strong contamination due to high anthropogenic activity such as mining and terrestrial influences into the coastal regions. Correlation coefficient shows that most of the elements are associated with each other except Ni and Pb. Factor analysis reveals that Mn, Zn, Fe, Cr, Pb and Cu are having a significant loading and it indicates that these elements are mainly derived from similar origin. The cluster analysis clearly indicated that the mining areas are grouped under cluster 2 and non-mining areas are clustered under group 1. Copyright © 2017 Elsevier Ltd. All rights reserved.

Ancient mantle in a modern arc: osmium isotopes in izu-bonin-mariana forearc peridotites

PubMed

Parkinson; Hawkesworth; Cohen

1998-09-25

Mantle peridotites drilled from the Izu-Bonin-Mariana forearc have unradiogenic 187Os/188Os ratios (0.1193 to 0.1273), which give Proterozoic model ages of 820 to 1230 million years ago. If these peridotites are residues from magmatism during the initiation of subduction 40 to 48 million years ago, then the mantle that melted was much more depleted in incompatible elements than the source of mid-ocean ridge basalts (MORB). This result indicates that osmium isotopes record information about ancient melting events in the convecting upper mantle not recorded by incompatible lithophile isotope tracers. Subduction zones may be a graveyard for ancient depleted mantle material, and portions of the convecting upper mantle may be less radiogenic in osmium isotopes than previously recognized.

Preliminary examination of the Yamato-86032 lunar meteorite. II - Major and trace element chemistry

NASA Technical Reports Server (NTRS)

Koeberl, Christian; Warren, Paul H.; Lindstrom, Marilyn M.; Spettel, Bernhard; Fukuoka, Takaaki

1989-01-01

Results of the chemical composition analysis of Yamato-86032, found in Antarctica in 1986, are summarized. The meteorite may be classified as an anorthositic breccia, but its trace element composition is different from the composition of the other known lunar meteorites. The major element chemistry of Y-86032 is similar to the other lunar meteorites, except for the iron content, which is lower by a factor of about 1.4. The abundances of incompatible and lithophile elements such as Zr, Hf, Ta, Th, or the REEs are very low and comparable to Y-82192/3. Other elements, in particular Fe, Ti, Sc, Cr, Mn, and Co, have lower abundances in Y-86032 than in Y-82192/3. Variations between individual analysis demonstrate that the rock itself is heterogeneous.

Nuclear reactor composite fuel assembly

DOEpatents

Burgess, Donn M.; Marr, Duane R.; Cappiello, Michael W.; Omberg, Ronald P.

1980-01-01

A core and composite fuel assembly for a liquid-cooled breeder nuclear reactor including a plurality of elongated coextending driver and breeder fuel elements arranged to form a generally polygonal bundle within a thin-walled duct. The breeder elements are larger in cross section than the driver elements, and each breeder element is laterally bounded by a number of the driver elements. Each driver element further includes structure for spacing the driver elements from adjacent fuel elements and, where adjacent, the thin-walled duct. A core made up of the fuel elements can advantageously include fissile fuel of only one enrichment, while varying the effective enrichment of any given assembly or core region, merely by varying the relative number and size of the driver and breeder elements.

Composition of Atmospheric Dust from Qatar in the Arabian Gulf

NASA Astrophysics Data System (ADS)

Yigiterhan, O.; Al-Ansari, I. S.; Abdel-Moati, M.; Al-Ansi, M.; Paul, B.; Nelson, A.; Turner, J.; Murray, J. W.; Alfoldy, B. Z.; Mahfouz, M. M. K.; Giamberini, M.

2015-12-01

Samples of atmospheric dust from Qatar have been collected and analyzed for major and trace elemental composition. Twenty-one samples were collected in 2014 and 2015 from Doha, Al Khor, Katara, Sealine, and Al Waab by a variety of techniques. Some samples were collected during the megastorms that occurred in April 2015. Back trajectories were determined for each sample using the NOAA HYSPLIT model over a 50 hour time interval. Our samples were about equally divided between northerly (n=12; northern Saudi Arabia, Kuwait or Iraq) and southerly (n=8; SE Saudi Arabia, United Arab Emirates and Oman) sources. One sample originated directly westward, in Saudi Arabia. Samples were microwave-assisted total acid digested (HF+HCl+HNO3) and analyzed by inductively coupled plasma-mass spectroscopy (ICP-MS) and inductively coupled plasma-optical emission spectroscopy (ICP-OES). There are only 12 out of 23 elements for which the Qatari dust was enriched relative to upper continental crust (UCC). Calcium was especially enriched at 400% relative to UCC. About 33% of the total sample mass was CaCO3, reflecting the composition of surface rocks in the source areas. Of the elements typically associated with anthropogenic activity, Ag, Ni and Zn were the most enriched relative to UCC, with enrichment factors of 182%, 233% and 209%, respectively. Others like Pb and V were not significantly enriched, with enrichment factors of 25% and 3%, respectively. The major elements Al, Mn and Fe were depleted relative to UCC because of the strong enrichment in CaCO3, with enrichment factors of -58%, -35% and -45% respectively. We separately averaged the samples with northern and southern origins to see if composition could be used to identify source. Only three elements had a statistical difference. Pb and Na were higher in the samples from the Se while Cr was higher in those from the north.

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.

Geochemical and isotopic constraints on island arc, synorogenic, post-orogenic and anorogenic granitoids in the Arabian Shield, Saudi Arabia

NASA Astrophysics Data System (ADS)

Robinson, F. A.; Foden, J. D.; Collins, A. S.

2015-04-01

The Arabian Shield preserves a protracted magmatic record of repeated amalgamation of juvenile subduction terranes that host granite intrusions ranging in age from the early Neoproterozoic to the Cambrian, which were emplaced into convergent and within-plate settings. Geochronology and whole-rock geochemistry of sampled Saudi Arabian granitoids define and distinguish four discrete age groups: 1) ~ 845-700 Ma island arc and synorogenic granitoids (IA + Syn), 2) ~ 640-610 Ma granitoids from the Nabitah and Halaban Suture (NHSG), 3) ~ 610-600 Ma post-orogenic perthitic (hypersolvus) granitoids (POPG), and 4) < 600 Ma anorogenic aegirine-bearing perthitic (hypersolvus) granitoids (AAPG). Groups 1, 2 and 3 include suites ranging from I-S- to A-type granites that have REE signatures typical of volcanic arc settings and show intra-suite variation that could be controlled by a combination of crustal assimilation and fractional crystallisation. Their mafic parental magmas have N-MORB-, or arc-tholeiite-like geochemistry. By contrast, group 4 A-type granites are more enriched in HREE and in incompatible elements such as Nb, Rb, Ga, Nd, Zr and Y and have lower Ce/Yb and higher Y/Nb ratios. These granitoids are interpreted to have been emplaced into within-plate and back-arc settings. Granitoid data also provide evidence that there may be two distinct mantle sources to the mafic parents of the granite suites. These are distinguished as contaminated and enriched mantle using Nb and Y and Nd isotopes. All granitoid suites are isotopically juvenile (ɛNd + 3 to + 6) and fall between the upper field crustal values of the Paleoproterozoic Khida terrane (ɛNd + 1) and contemporary depleted mantle. However, Nd isotopes distinguish contamination in group 1-3 mafic end-members beneath sutures which are interpreted to be derived from the contemporary MORB-type mantle wedge with subsequent crustal assimilation and fractionation to I- and A-type granitoids. The youngest (after 600 Ma) A-types (group 4) emplaced into extensional within-plate and back-arc settings require a new enriched mantle source that this study interprets to be associated with delamination.

Post-collisional magmatism in the Late Miocene Rodna-Bârgău district (East Carpathians, Romania): Geochemical constraints and petrogenetic models

NASA Astrophysics Data System (ADS)

Fedele, Lorenzo; Seghedi, Ioan; Chung, Sun-Lin; Laiena, Fabio; Lin, Te-Hsien; Morra, Vincenzo; Lustrino, Michele

2016-12-01

Post-collisional magmatism in the Late Miocene Rodna-Bârgău subvolcanic district (East Carpathians) gave rise to a wide variety of rock compositions, allowing recognition of four groups of calcalkaline rocks with distinctive petrography, mineral chemistry, whole-rock geochemistry and Sr-Nd-Hf isotope features. New U-Pb zircon datings, together with literature data, indicate that the emplacement of the four rock groups was basically contemporaneous in the 11.5-8 Ma time span. The low potassium group (LKG) includes the most abundant lithotypes of the area, ranging from basaltic andesite to dacite, characterized by K-poor tschermakitic amphibole, weak enrichment in LILE and LREE, relatively low 87Sr/86Sr, coupled with relatively high 143Nd/144Nd and 176Hf/177Hf. The high potassium group (HKG) includes amphibole-bearing microgabbro, amphibole andesite and amphibole- and biotite dacite, with K-richer magnesio-hastingsite to hastingsite amphibole, more marked enrichments in incompatible elements, higher 87Sr/86Sr and lower 143Nd/144Nd and 176Hf/177Hf. These two main rock groups seem to have originated from similar juxtaposed mantle sources, with the HKG possibly related to slightly more enriched domains (with higher H2O reflected by the higher modal amphibole) with respect to LKG (with higher plagioclase/amphibole ratios). The evolution of the two rock series involved also open-system processes, taking place mainly in the upper crust for the HKG, in the lower crust for LKG magmas. In addition, limited occurrences of generally younger strongly evolved peraluminous rhyolites and microgranites (Acid group) and sialic-dominated "leucocratic" andesites and dacites (LAD group) were also recognized to the opposite outermost areas of the district. These two latter rock groups were generated by the melting of a basic metamorphic crustal source (respectively in hydrous and anhydrous conditions), favored by the heat released by mantle melts from the adjoining central area. The peculiar distribution of the products of the four rock groups in well defined sectors argues for a strong control of the local crustal tectonic regime on magmatism, influenced by the change from a transpressional to trastensional stage.

Evidence for a single impact at the Cretaceous-Tertiary boundary from trace elements

NASA Technical Reports Server (NTRS)

Gilmour, Iain; Anders, Edward

1988-01-01

Not only meteoritic elements (Ir, Ni, Au, Pt metals), but also some patently non-meteoritic elements (As, Sb) are enriched at the K-T boundary. Eight enriched elements at 7 K-T sites were compared and it was found that: All have fairly constant proportions to Ir and Kilauea (invoked as an example of a volcanic source of Ir by opponents of the impact theory) has too little of 7 of these 8 elements to account for the boundary enrichments. The distribution of trace elements at the K-T boundary was reexamined using data from 11 sites for which comprehensive are available. The meteoritic component can be assessed by first normalizing the data to Ir, the most obviously extraterrestrial element, and then to Cl chondrites. The double normalization reduces the concentration range from 11 decades to 5 and also facilitates the identification of meteoritic elements. At sites where trace elements were analyzed in sub-divided samples of boundary clay, namely, Caravaca (SP), Stevns Klint (DK), Flaxbourne River (NZ) and Woodside Creek (NZ), Sb, As and Zn are well correlated with Ir across the boundary implying a common deposition mechanism. Elemental carbon is also enriched by up to 10,000 x in boundary clay from 5 K-T sides and is correlated with Ir across the boundary at Woodside Creek. While biomass would appear to be the primary fuel source for this carbon a contribution from a fossil fuel source may be necessary in order to account for the observed C abundance.

A glass spherule of questionable impact origin from the Apollo 15 landing site: Unique target mare basalt

USGS Publications Warehouse

Ryder, G.; Delano, J.W.; Warren, P.H.; Kallemeyn, G.W.; Dalrymple, G.B.

1996-01-01

A 6 mm-diameter dark spherule, 15434,28, from the regolith on the Apennine Front at the Apollo 15 landing site has a homogeneous glass interior with a 200 ??m-thick rind of devitrified or crystallized melt. The rind contains abundant small fragments of Apollo 15 olivine-normative mare basalt and rare volcanic Apollo 15 green glass. The glass interior of the spherule has the chemical composition, including a high FeO content and high CaO/Al2O3, of a mare basalt. Whereas the major element and Sc, Ni, and Co abundances are similar to those of low-Ti mare basalts, the incompatible elements and Sr abundances are similar to those of high-Ti mare basalts. The relative abundance patterns of the incompatible trace elements are distinct from any other lunar mare basalts or KREEP; among these distinctions are a much steeper slope of the heavy rare earth elements. The 15434,28 glass has abundances of the volatile element Zn consistent with both impact glasses and crystalline mare basalts, but much lower than in glasses of mare volcanic origin. The glass contains siderophile elements such as Ir in abundances only slightly higher than accepted lunar indigenous levels, and some, such as Au, are just below such upper limits. The age of the glass, determined by the 40Ar/39Ar laser incremental heating technique, is 1647 ?? 11 Ma (2 ??); it is expressed as an age spectrum of seventeen steps over 96% of the 39Ar released, unusual for an impact glass. Trapped argon is negligible. The undamaged nature of the sphere demonstrates that it must have spent most of its life buried in regolith; 38Ar cosmic ray exposure data suggest that it was buried at less than 2m but more than a few centimeters if a single depth is appropriate. That the spherule solidified to a glass is surprising; for such a mare composition, cooling at about 50??C s-1 is required to avoid crystallization, and barely attainable in such a large spherule. The low volatile abundances, slightly high siderophile abundances, and the young age are perhaps all most consistent with an impact origin, but nonetheless not absolutely definitive. The 15434,28 glass is distinct from the common yellow impact glasses at the Apollo 15 landing site, in particular in its lower abundances of incompatible elements and much younger age. If we accept an impact origin, then the trace element relative abundances preclude both typical KREEP and the common Apollo 15 yellow impact glass from contributing more than a few percent of the incompatible elements to potential mixtures. The melted part of any target must have consisted almost entirely of a variety (or varieties) of mare basalt or glass distinct from any known mare basalts or glasses, including Apollo 15 yellow volcanic glass, or mixtures of them. However, the rind inclusions, similar to materials of local origin, do suggest a source near the Apollo 15 landing site. An impact melt cannot have dissolved much, if any, of such inclusions. A lack of regolith materials in the rind and in the melt component suggest an immature source terrain. Thus, even for an impact origin, there is the possibility (though not requirement) that the volcanic target is younger than most mare plains. The crater Hadley C, 25 km away, is a potential source. If the 15434,28 glass is instead directly of volcanic origin, it represents an extremely young mare magma of a type previously undiscovered on the Moon.

Geochemistry of ultramafic xenoliths from Kapfenstein, Austria: evidence for a variety of upper mantle processes

NASA Astrophysics Data System (ADS)

Kurat, G.; Palme, H.; Spettel, B.; Baddenhausen, Hildegard; Hofmeister, H.; Palme, Christl; Wänke, H.

1980-01-01

Major, minor, and trace element contents have been determined in seven ultramafic xenoliths, the host basanite, and some mineral separates from xenoliths from Kapfenstein, Austria. Most of the xenoliths represent residues after extraction of different amounts of basaltic liquid. Within the sequence Iherzolite to harzburgite contents of Al, Ca, Ti, Na, Sc, V, Cr and the HREE decrease systematically with increasing Mg/Fe and decreasing Yb/Sc. Although all samples are depleted in highly incompatible elements, the less depleted end of our suite very closely approaches the chondritic Yb/Sc ratio and consequently the primitive upper mantle composition. Chromium behaved as a non-refractory element. Consequently it should have higher abundances in basalts than observed, suggesting that most basalts experienced Cr fractionation by chromite separation during ascent. Several processes have been active in addition to partial melting within the upper mantle beneath Kapfenstein: (1) a hornblendite has been identified as wet alkali-basaltic mobilisate; (2) an amphibole Iherzolite is the product of alkali-basalt metasomatism of a common depleted Iherzolite; (3) two amphibole Iherzolites contain evidence for rather pure water metasomatism of normal depleted Iherzolites; (4) a garnet-spinel websterite was a tholeiitic liquid trapped within the upper mantle and which suffered a subsequent partial melting event (partial remobilization of a mobilisate). (5) Abundances of highly incompatible elements are generally very irregular, indicating contamination of upper mantle rocks by percolating liquids (in the mantle). Weathering is an important source of contamination: e.g. U mobilization by percolating groundwater. Contamination of the xenoliths by the host basanite liquid can only amount to approximately 5.5 × 10 -4 parts. Distributions of minor and trace elements between different minerals apparently reflect equilibrium and vary with equilibration temperature.

Zonation of volatile and major elements in basaltic melt inclusions: a snapshot of syn-eruptive processes

NASA Astrophysics Data System (ADS)

Newcombe, M.; Fabbrizio, A.; Zhang, Y.; Le Voyer, M.; Guan, Y.; Ma, C.; Eiler, J. M.; Saal, A. E.; Stolper, E. M.

2011-12-01

Significant zonation in volatile and major elements has been discovered in olivine-hosted melt inclusions (MIs) from glassy pillow margins from the Siqueiros Fracture Zone [samples previously studied in 1]. For the most part, components that are compatible in olivine (e.g. MgO) are depleted at the edges of the zoned MIs relative to their centers, whereas components that are incompatible in olivine (e.g. Al2O3, SiO2, Na2O, and S) are enriched near the MI edges. H2O and F are exceptions in that they are incompatible, yet in several MIs they are depleted near the olivine-melt boundary. FeO and CaO are also exceptions in that they show complex features attributable to uphill diffusion. Another complexity is the similarity between the shapes of the SiO2 and Na2O profiles (despite significant differences in measured self and tracer diffusivities of these components [2, 3]), suggesting that the diffusion of these components is strongly coupled. All MIs from this sample suite exhibit zoning profiles, as do a suite of MIs from the Galapagos Islands and the inclusions studied in [4], so this feature may be common in rapidly quenched, glassy inclusions. Preservation of strong zonation in the Siqueiros MIs suggests that it formed in response to crystallization of olivine on the walls of the MIs during or just prior to eruption because, based on known diffusion coefficients, such profiles would be erased by diffusion on time scales on the order of 1 hr. The MgO concentration profiles in several Siqueiros MIs have been used to constrain the cooling history of the inclusions using the results of [5]. The profiles are consistent with an initial slow cooling rate followed by a period of more rapid cooling over a total timescale of ~10 min. Given that they are incompatible in olivine, the observed decreases in the concentrations of H2O and F toward the edges of some Siqueiros inclusions could suggest either uphill diffusion of H2O and F (as observed for H2O in [6] in a granitic composition) or loss of H2O and F into/through the host olivine (observed for H2O in [7-9]). The latter hypothesis would complement the results of [10], who observed elevated H2O and F in olivine adjacent to volatile-rich MIs. [1] Saal et al. (2002) Nature, 419, 451-455. [2] Lesher et al. (1996) Geochimica et Cosmochimica Acta, 60, 405-413. [3] Jambon (1982) Journal of Geophysical Research, 87, 10797-10810. [4] Mercier (2009) PhD thesis, Université Paris - Sud 11. [5] Chen & Zhang (2008) GCA, 72, 4756-4777. [6] Mungall et al. (1998) American Mineralogist, 83, 685-699. [7] Hauri (2002) Chemical Geology, 183, 115-141. [8] Massare et al. (2002) Chemical Geology, 183, 87-98. [9] Portnyagin et al. (2008) EPSL, 272, 541-552. [10] Le Voyer et al. (2010) AGU abstract #V23E-07.

Gallium isotopic evidence for the fate of moderately volatile elements in planetary bodies and refractory inclusions

NASA Astrophysics Data System (ADS)

Kato, Chizu; Moynier, Frédéric

2017-12-01

The abundance of moderately volatile elements, such as Zn and Ga, show variable depletion relative to CI between the Earth and primitive meteorite (chondrites) parent bodies. Furthermore, the first solar system solids, the calcium-aluminum-rich inclusions (CAIs), are surprisingly rich in volatile element considering that they formed under high temperatures. Here, we report the Ga elemental and isotopic composition of a wide variety of chondrites along with five individual CAIs to understand the origin of the volatile elements and to further characterize the enrichment of the volatile elements in high temperature condensates. The δ71Ga (permil deviation of the 71Ga/69Ga ratio from the Ga IPGP standard) of carbonaceous chondrites decreases in the order of CI >CM >CO >CV and is inversely correlated with the Al/Ga ratio. This implies that the Ga budget of the carbonaceous chondrites parent bodies were inherited from a two component mixing of a volatile rich reservoir enriched in heavy isotope of Ga and a volatile poor reservoir enriched in light isotope of Ga. Calcium-aluminum-rich inclusions are enriched in Ga and Zn compared to the bulk meteorite and are both highly isotopically fractionated with δ71Ga down to -3.56‰ and δ66Zn down to -0.74‰. The large enrichment in the light isotopes of Ga and Zn in the CAIs implies that the moderately volatile elements were introduced in the CAIs during condensation in the solar nebula as opposed to secondary processing in the meteorite parent body and supports a change in gas composition in which CAIs were formed.

Analysis of soil samples from Gebeng area using NAA technique

NASA Astrophysics Data System (ADS)

Elias, Md Suhaimi; Wo, Yii Mei; Hamzah, Mohd Suhaimi; Shukor, Shakirah Abd; Rahman, Shamsiah Ab; Salim, Nazaratul Ashifa Abdullah; Azman, Muhamad Azfar; Hashim, Azian

2017-01-01

Rapid development and urbanization will increase number of residence and industrial area. Without proper management and control of pollution, these will give an adverse effect to environment and human life. The objective of this study to identify and quantify key contaminants into the environment of the Gebeng area as a result of industrial and human activities. Gebeng area was gazetted as one of the industrial estate in Pahang state. Assessment of elemental pollution in soil of Gebeng area base on level of concentration, enrichment factor and geo-accumulation index. The enrichment factors (EFs) were determined by the elemental rationing method, whilst the geo-accumulation index (Igeo) by comparing of current to continental crustal average concentration of element. Twenty-seven of soil samples were collected from Gebeng area. Soil samples were analysed by using Neutron Activation Analyses (NAA) technique. The obtained data showed higher concentration of iron (Fe) due to abundance in soil compared to other elements. The results of enrichment factor showed that Gebeng area have enrich with elements of As, Br, Hf, Sb, Th and U. Base on the geo-accumulation index (Igeo) classification, the soil quality of Gebeng area can be classified as class 0, (uncontaminated) to Class 3, (moderately to heavily contaminated).

Mineralogy and petrology of cretaceous subsurface lamproite sills, southeastern Kansas, USA

USGS Publications Warehouse

Cullers, R.L.; Dorais, M.J.; Berendsen, P.; Chaudhuri, Sambhudas

1996-01-01

Cores and cuttings of lamproite sills and host sedimentary country rocks in southeastern Kansas from up to 312 m depth were analyzed for major elements in whole rocks and minerals, certain trace elements in whole rocks (including the REE) and Sr isotopic composition of the whole rocks. The lamproites are ultrapotassic (K2O/Na2O = 2.0-19.9), alkalic [molecular (K2O/Na2O)/Al2O3 = 1.3-2.8], enriched in mantle-incompatible elements (light REE, Ba, Rb, Sr, Th, Hf, Ta) and have nearly homogeneous initial Sr isotopic compositions (0.707764-0.708114). These lamproites could have formed by variable degrees of partial melting of harzburgite country rock and cross-cutting veins composed of phlogopite, K-Ti richterite, titanite, diopside, K-Ti silicates, or K-Ba-phosphate under high H2O/CO2 ratios and reducing conditions. Variability in melting of veins and wall rock and variable composition of the metasomatized veins could explain the significantly different composition of the Kansas lamproites. Least squares fractionation models preclude the derivation of the Kansas lamproites by fractional crystallization from magmas similar in composition to higher silica phlogopite-sanidine lamproites some believe to be primary lamproite melts found elsewhere. In all but one case, least squares fractionation models also preclude the derivation of magmas similar in composition to any of the Kansas lamproites from one another. A magma similar in composition to the average composition of the higher SiO2 Ecco Ranch lamproite (237.5-247.5 m depth) could, however, have marginally crystallized about 12% richterite, 12% sanidine, 7% diopside and 6% phlogopite to produce the average composition of the Guess lamproite (305-312 m depth). Lamproite from the Ecco Ranch core is internally fractionated in K2O, Al2O3, Ba, MgO, Fe2O3, Co and Cr most likely by crystal accumulation-removal of ferromagnesian minerals and sanidine. In contrast, the Guess core (305-312 m depth) has little fractionation throughout most of the sill except in several narrow zones. Lamproite in the Guess core has large enrichments in TiO2, Ba, REE, Th, Ta and Sc and depletions in MgO, Cr, Co and Rb possibly concentrated in these narrow zones during the last dregs of crystallization of this magma. The Ecco Ranch sill did not show any evidence of loss of volatiles or soluble elements into the country rock. This contrasts to the previously studied, shallow Silver City lamproite which did apparently lose H2O-rich fluid to the country rock. Perhaps a greater confining pressure and lesser amount of H2O-rich fluid prevented it from escaping.

Origin and migration of trace elements in the surface sediments of Majuro Atoll, Marshall Islands.

PubMed

Ito, Lisa; Omori, Takayuki; Yoneda, Minoru; Yamaguchi, Toru; Kobayashi, Ryuta; Takahashi, Yoshio

2018-07-01

The sediments of Majuro Atoll, Marshall Islands, consist of bioclastic materials, including foraminifera and coral debris. The sedimentary depth profiles of elements showed that various elements including zinc (Zn) and copper (Cu) were enriched in the upper layers of the islands of Majuro Atoll. Carbon-14 dating revealed that the sedimentation of the upper layer was completed before 1670 and 542 cal BP in Laura and Calalen, respectively. The enriched elements could be categorized by their origins: (a) terrestrial elements transported as dust (aluminum (Al) and rare earth elements (REEs)); (b) anthropogenic elements (Zn and Cu); and (c) elements supplied by seabirds (phosphorus (P)). From the results of the total amount of Al supplied to sediments for ca. 2000 years, Al in Majuro Atoll was suggested to be airborne origin. The enrichment factors of the elements normalized to Al concentration of continental crust showed that REEs were also transported as dust, while Zn and Cu were mainly of anthropogenic origin. The speciation analysis by X-ray absorption near-edge structure (XANES) showed the presence of Zn-Cu alloys originated from industrial products. It was also revealed that Zn was enriched in the surface due to anthropogenic emission after urbanization on Majuro Atoll and fixed by carbonate and phosphate at the upper layer, which inhibits migration of Zn into the deeper layer and its release to the groundwater and costal water. Hence, the fixation of heavy metals at the surface prevents their exposure to aquatic organisms and residents via fresh groundwater in the island. Copyright © 2018 Elsevier Ltd. All rights reserved.

Comparative Magma Oceanography

NASA Technical Reports Server (NTRS)

Jones, J. H.

1999-01-01

The question of whether the Earth ever passed through a magma ocean stage is of considerable interest. Geochemical evidence strongly suggests that the Moon had a magma ocean and the evidence is mounting that the same was true for Mars. Analyses of martian (SNC) meteorites have yielded insights into the differentiation history of Mars, and consequently, it is interesting to compare that planet to the Earth. Three primary features of Mars contrast strongly to those of the Earth: (i) the extremely ancient ages of the martian core, mantle, and crust (about 4.55 b.y.); (ii) the highly depleted nature of the martian mantle; and (iii) the extreme ranges of Nd isotopic compositions that arise within the crust and depleted mantle. The easiest way to explain the ages and diverse isotopic compositions of martian basalts is to postulate that Mars had an early magma ocean. Cumulates of this magma ocean were later remelted to form the SNC meteorite suite and some of these melts assimilated crustal materials enriched in incompatible elements. The REE pattern of the crust assimilated by these SNC magmas was LREE enriched. If this pattern is typical of the crust as a whole, the martian crust is probably similar in composition to melts generated by small degrees of partial melting (about 5%) of a primitive source. Higher degrees of partial melting would cause the crustal LREE pattern to be essentially flat. In the context of a magma ocean model, where large degrees of partial melting presumably prevailed, the crust would have to be dominated by late-stage, LREE-enriched residual liquids. Regardless of the exact physical setting, Nd and W isotopic evidence indicates that martian geochemical reservoirs must have formed early and that they have not been efficiently remixed since. The important point is that in both the Moon and Mars we see evidence of a magma ocean phase and that we recognize it as such. Several lines of theoretical inference point to an early Earth that was also hot and, perhaps, mostly molten. The Giant Impact hypothesis for the origin of the Moon offers a tremendous input of thermal energy and the same could be true for core formation. And current solar system models favor the formation of a limited number of large (about 1000 km) planetesimals that, upon accreting to Earth, would cause great heating, being lesser versions of the Giant Impact. Several lines of geochemical evidence do not favor this hot early Earth scenario. (i) Terrestrial man-tle xenoliths are sometimes nearly chondritic in their major element compositions, suggesting that these rocks have never been much molten. Large degrees of partial melting probably promote differentiation rather than homogenization. (ii) Unlike the case of Mars, the continental crust probably did not form as a highly fractionated residual liquid from a magma ocean (about 99% crystallization), but, rather, formed in multiple steps. [The simplest model for the formation of continental crust is complicated: (a) about 10% melting of a primitive mantle, making basalt; (b) hydrothermal alteration of that basalt, converting it to greenstone; and (c) 10% partial melting of that greenstone, producing tonalite.] This model is reinforced by the recent observation from old (about 4.1 b.y.) zircons that the early crust formed from an undepleted mantle having a chondritic Lu/Hf ratio. (iii) If the mantle were once differentiated by a magma ocean, the mantle xenolith suite requires that it subsequently be homogenized. The Os isotopic compositions of fertile spinel lherzolites place constraints on the timing of that homogenization. The Os isotopic composition of spinel lherzolites approaches that of chondrites and correlates with elements such as Lu and Al. As Lu and Al concentrations approach those of the primitive mantle, Os isotopic compositions approach chondritic. The Re and Os in these xenoliths were probably added as a late veneer. Thus, the mantle that received the late veneer must have been nearly chondritic in terms of its major elements (excluding Fe). If the mantle that the veneer was mixed into was not al-ready homogenized, then Os isotopes should not correlate with incompatible elements such as Al. Consequently, either early differentiation of the mantle did not occur or the homogenization of this differentiation must have occurred before the late veneer was added. The timing of the late veneer is itself uncertain but presumably postdated core formation at about 4.45 b.y. and did not postdate the 3.8-3.9 b.y. late bombardment of the Moon. This timing based on siderophile elements is consistent with the Hf isotopic evidence cited above. If the Earth, Moon and Mars had magma oceans, the Earth subsequently rehomogenized whereas the Moon and Mars did not. The simplest solution to this observation is that homogenization of igneous differentiates was never necessary on Earth, either because the hypothetical magma ocean never occurred or because this event did not produce mantle differentiation.

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.

Rare Earth Element Partitioning in Lunar Minerals: An Experimental Study

NASA Technical Reports Server (NTRS)

McIntosh, E. C.; Rapp, J. F.; Draper, D. S.

2016-01-01

The partitioning behavior of rare earth elements (REE) between minerals and melts is widely used to interpret the petrogenesis and geologic context of terrestrial and extra-terrestrial samples. REE are important tools for modelling the evolution of the lunar interior. The ubiquitous negative Eu anomaly in lunar basalts is one of the main lines of evidence to support the lunar magma ocean (LMO) hypothesis, by which the plagioclase-rich lunar highlands were formed as a flotation crust during differentiation of a global-scale magma ocean. The separation of plagioclase from the mafic cumulates is thought to be the source of the Eu depletion, as Eu is very compatible in plagioclase. Lunar basalts and volcanic glasses are commonly depleted in light REEs (LREE), and more enriched in heavy REEs (HREE). However, there is very little experimental data available on REE partitioning between lunar minerals and melts. In order to interpret the source of these distinctive REE patterns, and to model lunar petrogenetic processes, REE partition coefficients (D) between lunar minerals and melts are needed at conditions relevant to lunar processes. New data on D(sub REE) for plagioclase, and pyroxenes are now available, but there is limited available data for olivine/melt D(sub REE), particularly at pressures higher than 1 bar, and in Fe-rich and reduced compositions - all conditions relevant to the lunar mantle. Based on terrestrial data, REE are highly incompatible in olivine (i.e. D much less than 1), however olivine is the predominant mineral in the lunar interior, so it is important to understand whether it is capable of storing even small amounts of REE, and how the REEs might be fractionatied, in order to understand the trace element budget of the lunar interior. This abstract presents results from high-pressure and temperature experiments investigating REE partitioning between olivine and melt in a composition relevant to lunar magmatism.

Magmatic-hydrothermal fluid interaction and mineralization in alkali-syenite nodules from the Breccia Museo pyroclastic deposit, Naples, Italy: Chapter 7 in Volcanism in the Campania Plain — Vesuvius, Campi Flegrei and Ignimbrites

USGS Publications Warehouse

Fedele, Luca; Tarzia, Maurizio; Belkin, Harvey E.; De Vivo, Benedetto; Lima, Annamaria; Lowenstern, Jacob

2007-01-01

The Breccia Museo, a pyroclastic flow that crops out in the Campi Flegrei volcanic complex (Naples, Italy), contains alkali-syenite (trachyte) nodules with enrichment in Cl and incompatible elements (e.g., U, Zr, Th, and rare-earth elements). Zircon was dated at ≈52 ka, by U-Th isotope systematics using a SHRIMP. Scanning electron microscope and electron microprobe analysis of the constituent phases have documented the mineralogical and textural evolution of the nodules of feldspar and mafic accumulations on the magma chamber margins. Detailed electron microprobe data are given for alkali and plagioclase feldspar, salite to ferrosalite clinopyroxene, pargasite, ferrogargasite, magnesio-hastingsite hornblende amphibole, biotite mica, Cl-rich scapolite, and a member (probable davyne-type) of the cancrinite group. Detailed whole rock, major and minor element data are also presented for selected nodules. A wide variety of common and uncommon accessory minerals were identified such as zircon, baddeleyite, zirconolite, pollucite, sodalite, titanite, monazite, cheralite, apatite, titanomagnetite and its alteration products, scheelite, ferberite, uraninite/thorianite, uranpyrochlore, thorite, pyrite, chalcopyrite, and galena. Scanning electron microscope analysis of opened fluid inclusions identified halite, sylvite, anhydrite, tungstates, carbonates, silicates, sulfides, and phosphates; most are probably daughter minerals. Microthermometric determinations on secondary fluid inclusions hosted by alkali feldspar define a temperature regime dominated by hypersaline aqueous fluids. Fluid-inclusion temperature data and mineral-pair geothermometers for coexisting feldspars and hornblende and plagioclase were used to construct a pressure-temperature scenario for the development and evolution of the nodules. We have compared the environment of porphyry copper formation and the petrogenetic environment constructed for the studied nodules. The suite of ore minerals observed in the nodules supports a potential for mineralization, which is similar to that observed in the alkaline volcanic systems of southern Italy (Pantelleria, Pontine Archipelago, Mt. Somma-Vesuvius).

The Ge/Si ratio quantifies the role of recycled crust in the generation of MORBs

NASA Astrophysics Data System (ADS)

Yang, S.; Humayun, M.; Salters, V. J. M.

2017-12-01

Global MORBs cover a broad spectrum of incompatible element compositions from depleted [(La/Sm)N < 0.5] to enriched [(La/Sm)N 0.5-2]. Two explanations for the origin of the enriched mantle sources of E-MORBs from ridge segments not associated with plumes have been proposed: (1) re-fertilization of Depleted Mantle (DM) by infiltration of low-degree melts (<1%) from subducted crust, or (2) by entrainment of solid recycled crust in the Depleted Mantle (DM). Whether pyroxenite contributes melt to E-MORB can be resolved by chemically distinguishing between partial melts of a peridotite source vs. those of a lithologically heterogeneous source of peridotite and pyroxenite. In this study, we exploit the mineralogical preferences of elements like Ge and Si to distinguish melts formed from peridotite or pyroxenite. In-situ analyses of 60 elements in 319 MORB glasses from north (10-36 °N) Mid-Atlantic Ridge (MAR) and Mid-Cayman Rise were performed by LA-ICP-MS. Use of a large laser spot size (150 μm) and high repetition rate (50 Hz) yielded a low blank correction (< 5%) for Ge, and high external precision for the Ge/Si ratio (± 3%, 1σ) in MORB glasses. E-MORBs (6.4±0.2) are systematically lower in Ge/Si than D-MORBs (7.2±0.2), while N-MORBs fall in between and are not fully resolved from either D- or E-MORB. Based on experimental Ds, partial melts from pyroxenites are always lower in Ge/Si than partial melts from peridotites because Ge is more compatible in garnet and clinopyroxene than in olivine [1]. E-MORBs also have lower Sc abundances (37 vs. 43 ppm) but slightly higher Fe/Mn ratios (55 vs. 53) than D-MORBs, and lower La/Nb (0.6 vs. 1-2) and Sr/Nb (<20 vs. >40), consistent with addition of 27% pyroxenite-derived melts to a D-MORB-like composition. This requires that the amount of solid recycled garnet pyroxenite in a peridotite source is 12%. The Ge/Si ratio is a new tool that effectively discriminates between melts derived from peridotite sources and melts derived from pyroxenite sources. Extrapolating from the correlation between K2O/TiO2 and Ge/Si established in this study, we estimated the distribution of pyroxenite, solid recycled crust, in the mantle sources of global MORB segments, which reveals a mode of 3-4% pyroxenite in the MORB source. [1] Davis et al., 2013

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.

A middle Permian ophiolite fragment in Late Triassic greenschist- to blueschist-facies rocks in NW Turkey: An earlier pulse of suprasubduction-zone ophiolite formation in the Tethyan belt

NASA Astrophysics Data System (ADS)

Topuz, Gültekin; Okay, Aral I.; Schwarz, Winfried H.; Sunal, Gürsel; Altherr, Rainer; Kylander-Clark, Andrew R. C.

2018-02-01

The Eastern Mediterranean region within the Tethyan belt is characterised by two main pulses of suprasubduction-zone ophiolite formation during the Early-Middle Jurassic and Late Cretaceous. Despite vast exposures of the Permo-Triassic accretionary complexes, related suprasubduction-zone ophiolites and the timing of subduction initiation leading to the formation of Permo-Triassic accretionary complexes are unknown so far. Here we report on a 40 km long and 0.3 to 1.8 km wide metaophiolite fragment within transitional greenschist- to blueschist-facies oceanic rocks from NW Turkey. The metaophiolite fragment is made up mainly of serpentinite and minor dykes or stocks of strongly sheared metagabbro with mineral assemblages involving actinolite/winchite, chlorite, epidote, albite, titanite and phengite. The metagabbro displays (i) variable CaO and MgO contents, (ii) anomalously high Mg# (= 100 ∗ molar MgO/(MgO + FeOtot)) of 75-88, and (iii) positive Eu anomalies, together with low contents of incompatible elements such as Ti, P and Zr, suggesting derivation from former plagioclase cumulates. The serpentinites comprise serpentine, ± chlorite, ± talc, ± calcite and relict Cr-Al spinel surrounded by ferrichromite to magnetite. Relict Cr-Al spinels are characterised by (i) Cr/(Cr + Al) ratios of 0.45-0.56 and Mg/(Mg + Fe2 +) ratio of 0.76-0.22, (ii) variable contents of ZnO and MnO, and (iii) extremely low TiO2 contents. Zn and Mn contents are probably introduced into Cr-Al spinels during greenschist- to blueschist metamorphism. Compositional features of the serpentinite such as (i) Ca- and Al-depleted bulk compositions, (ii) concave U-shaped, chondrite-normalised rare earth element patterns (REE) with enrichment of light and heavy REEs, imply that serpentinites were probably derived from depleted peridotites which were refertilised by light rare earth element enriched melts in a suprasubduction-zone mantle wedge. U-Pb dating on igneous zircons from three metagabbro samples indicates igneous crystallisation at 262 Ma (middle Permian). Timing of the metamorphism is constrained by incremental 40Ar/39Ar dating on phengitic white mica at 201 Ma (latest Triassic). We conclude that the metaophiolite represents a fragment of middle Permian suprasubduction-zone oceanic lithosphere, involved in a latest Triassic subduction zone. These data, together with several reports in literature, indicate that the middle Permian was a time of suprasubduction-zone ophiolite formation in the Tethyan belt.

Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements

PubMed Central

Hayes, James E.; Trynka, Gosia; Vijai, Joseph; Offit, Kenneth; Raychaudhuri, Soumya; Klein, Robert J.

2015-01-01

Though numerous polymorphisms have been associated with risk of developing lymphoma, how these variants function to promote tumorigenesis is poorly understood. Here, we report that lymphoma risk SNPs, especially in the non-Hodgkin’s lymphoma subtype chronic lymphocytic leukemia, are significantly enriched for co-localization with epigenetic marks of active gene regulation. These enrichments were seen in a lymphoid-specific manner for numerous ENCODE datasets, including DNase-hypersensitivity as well as multiple segmentation-defined enhancer regions. Furthermore, we identify putatively functional SNPs that are both in regulatory elements in lymphocytes and are associated with gene expression changes in blood. We developed an algorithm, UES, that uses a Monte Carlo simulation approach to calculate the enrichment of previously identified risk SNPs in various functional elements. This multiscale approach integrating multiple datasets helps disentangle the underlying biology of lymphoma, and more broadly, is generally applicable to GWAS results from other diseases as well. PMID:26422229

Cannibalism of olivine-rich cumulate xenoliths during the 1998 eruption of Piton de la Fournaise (La Réunion hotspot): Implications for the generation of magma diversity

NASA Astrophysics Data System (ADS)

Salaün, A.; Villemant, B.; Semet, M. P.; Staudacher, T.

2010-12-01

Contrasting with its unusual isotopic homogeneity compared to other hotspot volcanoes, Piton de la Fournaise has produced a large diversity of basaltic magmas over its 0.5 Ma history: picrites and two types of transitional basalts with distinct petrological and chemical compositions. A minor group of evolved basalts (anomalous group of basalts or AGB) is enriched in both compatible (Mg, Fe, Ti, Cr, and Ni) and incompatible (K, Th, and La) elements and depleted in Ca and Si relative to the dominant group of evolved basalts. The 1998 eruption simultaneously produced the two basaltic types at two distinct vents (Hudson vent: AGB, Kapor vent: common basalt) but from the same feeding conduit. Glasses of both magmas are close in composition and belong to the single differentiation trend defined by all 1998-2007 glass compositions. Thermodynamic model (MELTS code) shows that AGB-type magmas cannot be produced by high pressure (> 1 GPa) clinopyroxene fractionation as previously proposed and that all melts of the 1998-2007 activity period are produced by low pressure (< 800 MPa) crystal fractionation from the most primitive basalt (MgO ~ 9%). Modal composition of 1998 lavas (mass balance calculation and SEM image analysis) and olivine crystal composition show that Hudson lavas have assimilated significant fractions of olivine xenocrysts contrary to Kapor lavas. In addition, the higher incompatible element contents of Hudson lavas suggest contamination by a differentiated (trachytic) melt. All AGB share the following characteristics: (i) evolved glass compositions, (ii) 5-10% olivine xenocrysts, and (iii) vents located in a narrow region at the summit of the edifice. They are interpreted as the result of the assimilation of olivine-rich xenoliths either by evolved melts or by basaltic melts contaminated by low fractions of differentiated melts produced from interstitial glass frequently coating cumulates minerals or resulting from partial melting of cumulates bearing pyroxene or plagioclase (wehrlitic to gabbroic cumulates). The scarcity of AGB magmas is attributed to their shallow transfer path in rarely intruded lateral zones of Piton de la Fournaise volcano: wehrlitic to gabbroic cumulates bodies are either heterogeneously distributed within the edifice or have been depleted in low melting point components in the 'Rift Zone' where most of the recent eruptive events are emplaced. These results emphasize the exceptional chemical homogeneity of the primary basaltic melt involved in volcanic activity of Piton de la Fournaise hotspot for 0.5 Ma and the increasingly recognized role of magma-wall rock interactions in erupted magma compositions.

Interaction of ultra-depleted MORBs with plagioclase: implications for CO2/Ba ratios

NASA Astrophysics Data System (ADS)

Shimizu, K.; Hauri, E.; Saal, A. E.; Perfit, M. R.; Hekinian, R.

2017-12-01

Carbon in Earth's upper mantle can significantly reduce its solidus temperature, which in turn can affect other physical properties through generation of partial melt. Carbon content in the depleted upper mantle can be estimated using ultra-depleted mid-ocean ridge basalt (UD-MORB) glasses and melt inclusions that are undersaturated in CO2. CO2 has been shown to behave as a highly incompatible element during mantle melting both through natural samples and experiments. Given its highly incompatible behavior, CO2/Ba and CO2/Nb ratios in CO2 undersaturated UD-MORBs have been used to estimate the CO2/Ba and CO2/Nb ratios and carbon content in Earth's upper mantle. A potential issue with part of this approach is the effect of melt-plagioclase chemical interaction on the CO2/Ba ratios in UD-MORBs. Plagioclase is ubiquitous in the oceanic crust and is enriched in Ba relative to other phases. Chemical interactions (assimilation and/or diffusion) between MORB melts and plagioclase bearing rocks have been shown to affect the Ba (and Sr and Eu) concentrations in MORBs, implying that such processes may also affect their CO2/Ba ratio. Hence, understanding the effect of chemical interaction between plagioclase and UD-MORBs is important for having better constraints on CO2/Ba ratio and carbon content in Earth's upper mantle. In this study, we report on the compositions of olivine-hosted melt inclusions and glasses from the Siqueiros and Garrett transform faults. A subset of melt inclusions in lavas from both transform faults show potential signatures of chemical interaction with plagioclase such as low CO2/Ba, Nb/Ba, and Nd/Sr. CO2 degassing cannot explain the low CO2/Ba ratio in the samples as they are undersaturated in CO2. To better understand the effect of chemical interaction with plagioclase on the composition of UD-MORBs, we model end-member scenarios, which are (1) assimilation of plagioclase and (2) diffusion of elements from plagioclase into the UD-MORBs. In general, the trends produced by these end-member scenarios bracket those observed in the samples (trends between CO2/Ba, Nb/Ba, and Nd/Sr as well as between Al2O3, FeO, and MgO). Hence, chemical interaction with plagioclase may affect the CO2/Ba ratio in UD-MORBs, and care should be taken to evaluate this effect using Nd/Sr and Nb/Ba ratios.

Chemical evolution of the Earth: Equilibrium or disequilibrium process?

NASA Technical Reports Server (NTRS)

Sato, M.

1985-01-01

To explain the apparent chemical incompatibility of the Earth's core and mantle or the disequilibrium process, various core forming mechanisms have been proposed, i.e., rapid disequilibrium sinking of molten iron, an oxidized core or protocore materials, and meteorite contamination of the upper mantle after separation from the core. Adopting concepts used in steady state thermodynamics, a method is devised for evaluating how elements should distribute stable in the Earth's interior for the present gradients of temperature, pressure, and gravitational acceleration. Thermochemical modeling gives useful insights into the nature of chemical evolution of the Earth without overly speculative assumptions. Further work must be done to reconcile siderophile elements, rare gases, and possible light elements in the outer core.

The Hasan Dagi stratovolcano (Central Anatolia, Turkey): evolution from calc-alkaline to alkaline magmatism in a collision zone

NASA Astrophysics Data System (ADS)

Deniel, Catherine; Aydar, Erkan; Gourgaud, Alain

1998-12-01

The Hasan Dagi volcano is one of the two large Plio-Quaternary volcanoes in Cappadocia (Central Anatolia, Turkey). Three stages of edifice construction have been identified for this volcano: Paleovolcano, Mesovolcano and Neovolcano. Most samples from Hasan Dagi volcano are calc-alkaline and define an almost complete trend from basaltic andesite to rhyolite. However, the more recent (Neovolcano) mafic samples are alkaline basalts. The mineralogical and geochemical characteristics of the oldest lavas (Keçikalesi (13 Ma) and Paleo-Hasan Dagi (7 Ma)) are significantly different from those of the younger lavas (Meso- and Neo-Hasan Dagi (<1 Ma)). Calcic plagioclase and pigeonite are typically observed in these older lavas. The Paleovolcano basalts are depleted in alkalis and display a tholeiitic tendency whereas the differentiated lavas are depleted in Na 2O but enriched in K 2O compared to younger lavas. There is an evolution through time towards higher TiO 2, Fe 2O 3*, MgO, Na 2O and K 2O and lower Al 2O 3 and SiO 2 which is reflected in the basalt compositions. All the basalts display multi-element patterns typical of continental margin magmas with a significant enrichment in LILE (K, Rb, Ba and Th) and LREE and strong (Paleovolcano) to moderate (Meso- and Neovolcano) negative Nb, Zr and Ti anomalies. However, the younger basalts are the most enriched in incompatible elements, in agreement with their alkaline affinities and do not systematically display negative HFSE anomalies. REE data suggest an hydrous amphibole-bearing crystallization history for both Meso- and Neovolcano lavas. The distinction between the older and younger lavas is also apparent in trace element ratios such as Nb/Y, Ti/Y and Th/Y. These ratios indicate the role of a subducted component±crustal contamination in the genesis of the Hasan Dagi lavas, particularly for the oldest lavas (Keçikalesi and Paleo-Hasan Dagi). The decreasing influence of this component through time, over the last 6-7 m.y., has been accompanied by an increasing contribution of melt-enriched lithosphere. Although the range of variation of Sr, Nd and Pb isotopic ratios is small (0.70457-0.70515; 0.51262-0.51273; 18.80-18.94; 15.64-15.69; 38.87-39.10), it also reflects the evolution of the magma sources through time. Indeed, the youngest (Neovolcano) and most primitive basalts display significantly lower 87Sr/ 86Sr than the Paleo- and Mesovolcano basalts, whereas the Mesovolcano basalts display more radiogenic Pb than Paleovolcano samples. Magma mixing processes between initially heterogeneous and/or variably contaminated magmas may account for the genesis of the less differentiated and intermediate lavas (48-57% SiO 2). Meso- and Neovolcano differentiated lavas (60-68% SiO 2) are either derived from the analyzed basalts or from more primitive and more depleted magmas by fractional crystallization±some crustal contamination (AFC). Furthermore, the highly differentiated samples (72-75% SiO 2) are not strongly contaminated. The strong calc-alkaline character of Hasan Dagi lavas, in the absence of contemporaneous subduction, must reflect the heritage of the early subduction of the Afro-Arabian plate under the Eurasian plate. The evolution towards alkaline compositions through time is clearly related to the development of extensional tectonics in Central Anatolia in the Late Miocene.

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.

Enrichment of short interspersed transposable elements to embryonic stem cell-specific hypomethylated gene regions.

PubMed

Muramoto, Hiroki; Yagi, Shintaro; Hirabayashi, Keiji; Sato, Shinya; Ohgane, Jun; Tanaka, Satoshi; Shiota, Kunio

2010-08-01

Embryonic stem cells (ESCs) have a distinctive epigenome, which includes their genome-wide DNA methylation modification status, as represented by the ESC-specific hypomethylation of tissue-dependent and differentially methylated regions (T-DMRs) of Pou5f1 and Nanog. Here, we conducted a genome-wide investigation of sequence characteristics associated with T-DMRs that were differentially methylated between ESCs and somatic cells, by focusing on transposable elements including short interspersed elements (SINEs), long interspersed elements (LINEs) and long terminal repeats (LTRs). We found that hypomethylated T-DMRs were predominantly present in SINE-rich/LINE-poor genomic loci. The enrichment for SINEs spread over 300 kb in cis and there existed SINE-rich genomic domains spreading continuously over 1 Mb, which contained multiple hypomethylated T-DMRs. The characterization of sequence information showed that the enriched SINEs were relatively CpG rich and belonged to specific subfamilies. A subset of the enriched SINEs were hypomethylated T-DMRs in ESCs at Dppa3 gene locus, although SINEs are overall methylated in both ESCs and the liver. In conclusion, we propose that SINE enrichment is the genomic property of regions harboring hypomethylated T-DMRs in ESCs, which is a novel aspect of the ESC-specific epigenomic information.

HFSE systematics of rutile-bearing eclogites: New insights into subduction zone processes and implications for the earth’s HFSE budget

NASA Astrophysics Data System (ADS)

Schmidt, Alexander; Weyer, Stefan; John, Timm; Brey, Gerhard P.

2009-01-01

The depleted mantle and the continental crust are generally thought to balance the budget of refractory and lithophile elements of the Bulk Silicate Earth (BSE), resulting in complementary trace element patterns. However, the two high field strength elements (HFSE) niobium and tantalum appear to contradict this mass balance. All reservoirs of the silicate Earth exhibit subchondritic Nb/Ta ratios, possibly as a result of Nb depletion. In this study a series of nineteen orogenic MORB-type eclogites from different localities was analyzed to determine their HFSE concentrations and to contribute to the question of whether subducted oceanic crust could form a hidden reservoir to account for the mass imbalance of Nb/Ta between BSE and the chondritic reservoir. Concentrations of HFSE were analyzed with isotope dilution (ID) techniques. Additionally, LA-ICPMS analyses of clinopyroxene, garnet and rutile have been performed. Rutile is by far the major host for Nb and Ta in all analyzed eclogites. However, many rutiles revealed zoning in Nb/Ta ratios, with cores being higher than rims. Accordingly, in situ analyses of rutiles have to be evaluated carefully and rutile cores do not necessarily reflect a bulk rock Nb and Ta composition, although over 90% of these elements reside in rutile. The HFSE concentration data in bulk rocks show that the orogenic eclogites have subchondritic Nb/Ta ratios and near chondritic Zr/Hf ratios. The investigated eclogites show neither enrichment of Nb compared to similarly incompatible elements (e.g. La), nor fractionation of Nb/Ta ratios relative to MOR-basalts, the likely precursor of these rocks. This indicates that during the conversion of the oceanic crust to eclogites in most cases, (1) HFSE and REE have similar mobility on average, possibly because both element groups remain in the down going slab, and (2) no significant fractionation of Nb/Ta occurs in subducted oceanic crust. With an average Nb/Ta ratio of 14.2 ± 1.4 (2s.e.), the investigated eclogites cannot balance the differences between BSE and chondrite. Additionally, as their average Nb/Ta is indistinguishable from the Nb/Ta of MORB, they are also an unlikely candidate to balance the potentially small differences in Nb/Ta between the continental crust and the mantle.

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

Phelan, J.M.

A high volume sampling system was developed for the collection of volcanic plume aerosols from an aircraft sampling platform. Concentrations of up to 30 elements on particles were determined simultaneously with gas-phase concentrations of S, Cl, and Br in the quiescent plumes of five active volcanoes: Mount St. Helens, US; Arenal and Poas, Costa Rica; Colima and El Chichon, Mexico. Volatile and chalcophilic elements were found to be highly enriched, relative to average crustal and bulk pyroclastic material, in the quiescent plumes of all volcanoes studied. Enriched volatile elements were found to be primarily associated with fine (less than ormore » equal to 3-..mu..m diam) particles, those expected to have the longest residence times in the atmosphere. Samples were also collected using the aircraft sampling system in background, mid-tropospheric air. Analysis of these samples revealed that many of the same elements that are enriched in volcanic plumes are also enriched in clean, relatively remote aerosols collected in the free troposphere (5-7 km). Concentrations of sulfates made in the North American free troposphere (280 ng/m/sup 3/) approach those measured at remote background sites.« less

An experimental investigation of fractionation by sputter deposition. [application to solar wind irradiation of lunar soil

NASA Technical Reports Server (NTRS)

Paruso, D. M.; Cassidy, W. A.; Hapke, B. W.

1978-01-01

Artificial glass targets composed of elements varying widely in atomic weight were irradiated at an angle of incidence of 45 deg by 2-keV hydrogen ions at a current density of .33 mA/sq cm, and sputtered atoms were caught on a molybdenum film. Analyses of the sputter-deposited films and unsputtered target glasses were carried out by electron microprobe. The backward-sputtered component was found to be enriched in elements of low atomic weight, while the forward-sputtered component was enriched in heavy atoms. These results indicate that at the lunar surface lighter elements and isotopes would tend to be ejected in backward directions, escaping directly through the openings which admit bombarding ions without first striking an adjacent grain surface; heavy elements and isotopes would be forward-sputtered deeper into the soil and be preferentially retained, contributing to the reported enrichments of heavy elements and isotopes. Additional results show that the binding energy of an element in its oxide form influences the sticking coefficient of a sputtered atom; elements of low binding energy are likely to desorb, while elements of high binding energy tend to stick to the first bounce surface.

Elemental ratios and enrichment factors in aerosols from the US-GEOTRACES North Atlantic transects

NASA Astrophysics Data System (ADS)

Shelley, Rachel U.; Morton, Peter L.; Landing, William M.

2015-06-01

The North Atlantic receives the highest aerosol (dust) input of all the oceanic basins. Dust deposition provides essential bioactive elements, as well as pollution-derived elements, to the surface ocean. The arid regions of North Africa are the predominant source of dust to the North Atlantic Ocean. In this study, we describe the elemental composition (Li, Na, Mg, Al, P, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Rb, Sr, Cd, Sn, Sb, Cs, Ba, La, Ce, Nd, Pb, Th, U) of the bulk aerosol from samples collected during the US-GEOTRACES North Atlantic Zonal Transect (2010/11) in order to highlight the differences between a Saharan dust end-member and the reported elemental composition of the upper continental crust (UCC), and the implications this has for identifying trace element enrichment in aerosols across the North Atlantic basin. As aerosol titanium (Ti) is less soluble than aerosol aluminum (Al), it is a more conservative tracer for lithogenic aerosols and trace element-to-Ti ratios. However, the presence of Ti-rich fine aerosols can confound the interpretation of elemental enrichments, making Al a more robust tracer of aerosol lithogenic material in this region.

Degassing history of water, sulfur, and carbon in submarine lavas from Kilauea Volcano, Hawaii

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

Dixon, J.E.; Stolper, E.M.; Clague, D.A.

1991-05-01

Major, minor, and dissolved volatile element concentrations were measured in tholeiitic glasses from the submarine portion (Puna Ridge) of the east rift zone of Kilauea Volcano, Hawaii. Dissolved H{sub 2}O and S concentrations display a wide range relative to nonvolatile incompatible elements at all depths. This range cannot be readily explained by fractional crystallization, degassing of H{sub 2}O and S during eruption on the seafloor, or source region heterogeneities. Dissolved CO{sub 2} concentrations, in contrast, show a positive correlation with eruption depth and typically agree within error with the solubility at that depth. The authors propose that most magmas alongmore » the Puna Ridge result from (1) mixing of a relatively volatile-rich, undegassed component with magmas that experienced low pressure (perhaps subaerial) degassing during which substantial H{sub 2}O, S, and CO{sub 2} were lost, followed by (2) fractional crystallization of olivine, clinopyroxene, and plagioclase from this mixture to generate a residual liquid; and (3) further degassing, principally of CO{sub 2} for samples erupted deeper than 1,000 m, during eruption on the seafloor. They predict that average Kilauean primary magmas with 16% MgO contain {approximately}0.47 wt % H{sub 2}0, {approximately}900 ppm S, and have {delta}D values of {approximately}{minus}30 to {minus}40%. The model predicts that submarine lavas from wholly submarine volcanoes (i.e., Loihi), for which there is no opportunity to generate the degassed end member by low pressure degassing, will be enriched in volatiles relative to those from volcanoes whose summits have breached the sea surface (i.e., Kilauea and Mauna Loa).« less

Constraints on the source of Cu in a submarine magmatic-hydrothermal system, Brothers volcano, Kermadec island arc

NASA Astrophysics Data System (ADS)

Keith, Manuel; Haase, Karsten M.; Klemd, Reiner; Smith, Daniel J.; Schwarz-Schampera, Ulrich; Bach, Wolfgang

2018-05-01

Most magmatic-hydrothermal Cu deposits are genetically linked to arc magmas. However, most continental or oceanic arc magmas are barren, and hence new methods have to be developed to distinguish between barren and mineralised arc systems. Source composition, melting conditions, the timing of S saturation and an initial chalcophile element-enrichment represent important parameters that control the potential of a subduction setting to host an economically valuable deposit. Brothers volcano in the Kermadec island arc is one of the best-studied examples of arc-related submarine magmatic-hydrothermal activity. This study, for the first time, compares the chemical and mineralogical composition of the Brothers seafloor massive sulphides and the associated dacitic to rhyolitic lavas that host the hydrothermal system. Incompatible trace element ratios, such as La/Sm and Ce/Pb, indicate that the basaltic melts from L'Esperance volcano may represent a parental analogue to the more evolved Brothers lavas. Copper-rich magmatic sulphides (Cu > 2 wt%) identified in fresh volcanic glass and phenocryst phases, such as clinopyroxene, plagioclase and Fe-Ti oxide suggest that the surrounding lavas that host the Brothers hydrothermal system represent a potential Cu source for the sulphide ores at the seafloor. Thermodynamic calculations reveal that the Brothers melts reached volatile saturation during their evolution. Melt inclusion data and the occurrence of sulphides along vesicle margins indicate that an exsolving volatile phase extracted Cu from the silicate melt and probably contributed it to the overlying hydrothermal system. Hence, the formation of the Cu-rich seafloor massive sulphides (up to 35.6 wt%) is probably due to the contribution of Cu from a bimodal source including wall rock leaching and magmatic degassing, in a mineralisation style that is hybrid between Cyprus-type volcanic-hosted massive sulphide and subaerial epithermal-porphyry deposits.

Vestiges of the proto-Caribbean seaway: Origin of the San Souci Volcanic Group, Trinidad

NASA Astrophysics Data System (ADS)

Neill, Iain; Kerr, Andrew C.; Chamberlain, Kevin R.; Schmitt, Axel K.; Urbani, Franco; Hastie, Alan R.; Pindell, James L.; Barry, Tiffany L.; Millar, Ian L.

2014-06-01

Outcrops of volcanic-hypabyssal rocks in Trinidad document the opening of the proto-Caribbean seaway during Jurassic-Cretaceous break-up of the Americas. The San Souci Group on the northern coast of Trinidad comprises the San Souci Volcanic Formation (SSVF) and passive margin sediments of the ~ 130-125 Ma Toco Formation. The Group was trapped at the leading edge of the Pacific-derived Caribbean Plate during the Cretaceous-Palaeogene, colliding with the para-autochthonous margin of Trinidad during the Oligocene-Miocene. In-situ U-Pb ion probe dating of micro-zircons from a mafic volcanic breccia reveal the SSVF crystallised at 135.0 ± 7.3 Ma. The age of the SSVF is within error of the age of the Toco Formation. Assuming a conformable contact, geodynamic models indicate a likely origin for the SSVF on the passive margin close to the northern tip of South America. Immobile element and Nd-Hf radiogenic isotope signatures of the mafic rocks indicate the SSVF was formed by ≪10% partial melting of a heterogeneous spinel peridotite source with no subduction or continental lithospheric mantle component. Felsic breccias within the SSVF are more enriched in incompatible elements, with isotope signatures that are less radiogenic than the mafic rocks of the SSVF. The felsic rocks may be derived from re-melting of mafic crust. Although geochemical comparisons are drawn here with proto-Caribbean igneous outcrops in Venezuela and elsewhere in the Caribbean more work is needed to elucidate the development of the proto-Caribbean seaway and its rifted margins. In particular, ion probe dating of micro-zircons may yield valuable insights into magmatism and metamorphism in the Caribbean, and in altered basaltic terranes more generally.

Geochemical constraints on the origin of high-Mg andesites in the southernmost Okinawa Trough

NASA Astrophysics Data System (ADS)

Chu, C.; Chung, S.; Shinjo, R.; Gallet, S.; Wang, S.; Chen, C.

2007-12-01

The Okinawa Trough, extending from SW Kyushu to NE Taiwan, is a backarc basin of the Ryukyu arc-trench system due to subduction of the Philippine Sea plate under the Eurasian plate. The southernmost part of the Okinawa Trough (SPOT), however, does not situate in a simple backarc setting but is an embryonic rift zone in which early arc volcanism takes place. Kueishantao that consists mainly of andesitic flows dated to be ~7000 yr old is an emerged volcanic islet thus formed in SPOT. Here we report whole-rock major and trace element, and Sr-Nd-Pb-Hf isotope compositions of the Kueishantao andesites. Some of the samples have unexpectedly high magnesium, with MgO ≥ 5 wt.% and Mg# > 0.5, relative to their silica contents (SiO2 ~ 60 wt.%), so can be coined as high-Mg andesites (HMAs). These HMAs display enrichments in Cs, Rb, Ba, Th, U, LREE and Pb, and depletions in HFSE, in the incompatible element variation diagram. Their overall geochemical compositions are similar to those of the mean continental crust proposed by Rudnick and Fountain (1995). The HMAs have uniform radiogenic isotope ratios, with low ÕɛNd (-4.3 to -5.0), low ÕɛHf (-0.9 to -2.4), and high 87Sr/86Sr (~0.706) and 206Pb/204Pb (~18.75). In contrast to previous notion that calls for significant contamination of upper continental crust in the magma chamber, we propose the Kueishantao HMAs to have resulted from partial melting of the subducted sediments and altered Philippine Sea crust followed by melt-mantle interaction in the mantle wedge. This interpretation is consistent with seismic tomographic results under the SPOT region marking with a combination of collision/extension/subduction tectonic context off NE Taiwan.

A chilled margin of komatiite and Mg-rich basaltic andesite in the western Bushveld Complex, South Africa

NASA Astrophysics Data System (ADS)

Maier, W. D.; Barnes, S.-J.; Karykowski, B. T.

2016-06-01

A chill sequence at the base of the Lower Zone of the western Bushveld Complex at Union Section, South Africa, contains aphanitic Mg-rich basaltic andesite and spinifex-textured komatiite. The basaltic andesite has an average composition of 15.2 % MgO, 52.8 % SiO2, 1205 ppm Cr, and 361 ppm Ni, whereas the komatiite has 18.7 % MgO, 1515 ppm Cr, and 410 ppm Ni. Both rock types have very low concentrations of immobile incompatible elements (0.14-0.72 ppm Nb, 7-31 ppm Zr, 0.34-0.69 ppm Th, 0.23-0.27 wt% TiO2), but high PGE contents (19-23 ppb Pt, 15-16 ppb Pd) and Pt/Pd ratios (Pt/Pd 1.4). Strontium and S isotopes show enriched signatures relative to most other Lower Zone rocks. The rocks could represent a ~20 % partial melt of subcontinental lithospheric mantle. This would match the PGE content of the rocks. However, this model is inconsistent with the high SiO2, Fe, and Na2O contents and, in particular, the low K2O, Zr, Hf, Nb, Ta, Th, LREE, Rb, and Ba contents of the rocks. Alternatively, the chills could represent a komatiitic magma derived from the asthenosphere that underwent assimilation of the quartzitic floor accompanied by crystallization of olivine and chromite. This model is consistent with the lithophile elements and the elevated Sr and S isotopic signatures of the rocks. However, in order to account for the high Pt and Pd contents of the magma, the mantle must have been twice as rich in PGE as the current estimate for PUM, possibly due to a component of incompletely equilibrated late veneer.

Partial melting of TTG gneisses: crustal contamination and the production of granitic melts

NASA Astrophysics Data System (ADS)

Meade, F. C.; Masotta, M.; Troll, V. R.; Freda, C.; Johnson, T. E.; Dahren, B.

2011-12-01

Understanding partial melting of ancient TTG gneiss terranes is crucial when considering crustal contamination in volcanic systems, as these rocks are unlikely to melt completely at magmatic temperatures (1000-1200 °C) and crustal pressures (<500 MPa). Variations in the bulk composition of the gneiss, magma temperature, pressure (depth) and the composition and abundance of any fluids present will produce a variety of melt compositions, from partial melts enriched in incompatible elements to more complete melts, nearing the bulk chemistry of the parent gneiss. We have used piston cylinder experiments to simulate partial melting in a suite of 12 gneisses from NW Scotland (Lewisian) and Eastern Greenland (Ammassalik, Liverpool Land) under magma chamber temperature and pressure conditions (P=200 MPa, T=975 °C). These gneisses form the basement to much of the North Atlantic Igneous Province, where crustal contamination of magmas was commonplace but the composition of the crustal partial melts are poorly constrained [1]. The experiments produced partial melts in all samples (e.g. Fig 1). Electron microprobe analyses of glasses indicate they are compositionally heterogeneous and are significantly different from the whole rock chemistry of the parent gneisses. The melts have variably evolved compositions but are typically trachy-dacitic to rhyolitic (granitic). This integrated petrological, experimental and in-situ geochemical approach allows quantification of the processes of partial melting of TTG gneiss in a volcanic context, providing accurate major/trace element and isotopic (Sr, Pb) end-members for modeling crustal contamination. The experimental melts and restites will be compared geochemically with a suite of natural TTG gneisses, providing constraints on the extent to which the gneisses have produced and subsequently lost melt. [1] Geldmacher et al. (2002) Scottish Journal of Geology, v.38, p.55-61.

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.

Geochemistry and evolution of MORB-type eclogites from the Münchberg Massif, southern Germany

NASA Astrophysics Data System (ADS)

Stosch, H.-G.; Lugmair, G. W.

1990-08-01

In the Münchberg Massif in the Variscan foldbelt of southern Germany two varieties of eclogite are known which are intercalated with amphibolite-facies meta-igneous and meta-sedimentary rocks: a dark kyanite-free and a lighter colored kyanite-bearing type. Kyanite-free eclogites, which are discussed here, have a major and trace element composition which suggests derivation from ocean-floor basalts with melt to cumulate compositions. Internal Sm sbnd Nd isochrons (clinopyroxene-amphibole-garnet) and one Rb sbnd Sr isochron (clinopyroxene-amphibole-mica) yield eclogitization ages in the range of 380 to 395 Ma. Thus, the age of eclogitization is only marginally higher ( < 15 Ma) than the age of amphibolite-facies metamorphism in the Münchberg Massif as derived from K sbnd Ar ages of amphiboles and micas from metasediments and meta-igneous rocks. A seven point whole-rock Sm sbnd Nd isochron for one eclogite body results in an age of 480 ± 23Ma with an initial ɛ Nd of 8.7 ± 0.6 and is likely to record the age of igneous formation of the eclogite protoliths. Sr isotopic compositions back-calculated to that time are anomalously high and variable if compared to Nd isotopes. This can be explained by alteration with an aqueous or fluid phase with high 87Sr 86Sr , most likely seawater, either during igneous formation in an oceanic rift environment or subduction-related eclogitization. In addition, some eclogites show a marked enrichment of incompatible, immobile elements and plot far below the whole-rock Sm sbnd Nd isochron. These features are ascribed to the presence of an evolved crustal component, probably acquired during extrusion of the basaltic protoliths by mixing with country-rock gneisses.

Geochemistry of ferromanganese nodule-sediment pairs from Central Indian Ocean Basin

NASA Astrophysics Data System (ADS)

Pattan, J. N.; Parthiban, G.

2011-01-01

Fourteen ferromanganese nodule-sediment pairs from different sedimentary environments such as siliceous ooze (11), calcareous ooze (two) and red clay (one) from Central Indian Ocean Basin (CIOB) were analysed for major, trace and rare earth elements (REE) to understand the possible elemental relationship between them. Nodules from siliceous and calcareous ooze are diagenetic to early diagenetic whereas, nodule from red clay is of hydrogenetic origin. Si, Al and Ba are enriched in the sediments compared to associated nodules; K and Na are almost in the similar range in nodule-sediment pairs and Mn, Fe, Ti, Mg, P, Ni, Cu, Mo, Zn, Co, Pb, Sr, V, Y, Li and REEs are all enriched in nodules compared to associated sediments (siliceous and calcareous). Major portion of Si, Al and K in both nodules and sediments appear to be of terrigenous nature. The elements which are highly enriched in the nodules compared to associated sediments from both siliceous and calcareous ooze are Mo - (307, 273), Ni - (71, 125), Mn - (64, 87), Cu - (43, 80), Co - (23, 75), Pb - (15, 24), Zn - (9, 11) and V - (8, 19) respectively. These high enrichment ratios of elements could be due to effective diagenetic supply of metals from the underlying sediment to the nodule. Enrichment ratios of transition metals and REEs in the nodule to sediment are higher in CIOB compared to Pacific and Atlantic Ocean. Nodule from red clay, exhibit very small enrichment ratio of four with Mn and Ce while, Al, Fe, Ti, Ca, Na, K, Mg, P, Zn, Co, V, Y and REE are all enriched in red clay compared to associated nodule. This is probably due to presence of abundant smectite, fish teeth, micronodules and phillipsite in the red clay. The strong positive correlation ( r ⩾ 0.8) of Mn with Ni, Cu, Zn and Mo and a convex pattern of shale-normalized REE pattern with positive Ce-anomaly of siliceous ooze could be due to presence of abundant manganese micronodules. None of the major trace and REE exhibits any type of inter-elemental relationship between nodule and sediment pairs. Therefore, it may not be appropriate to correlate elemental behaviour between these pairs.

Timing of Precambrian melt depletion and Phanerozoic refertilization events in the lithospheric mantle of the Wyoming Craton and adjacent Central Plains Orogen

USGS Publications Warehouse

Carlson, R.W.; Irving, A.J.; Schulze, D.J.; Hearn, B.C.

2004-01-01

Garnet peridotite xenoliths from the Sloan kimberlite (Colorado) are variably depleted in their major magmaphile (Ca, Al) element compositions with whole rock Re-depletion model ages generally consistent with this depletion occurring in the mid-Proterozoic. Unlike many lithospheric peridotites, the Sloan samples are also depleted in incompatible trace elements, as shown by the composition of separated garnet and clinopyroxene. Most of the Sloan peridotites have intermineral Sm-Nd and Lu-Hf isotope systematics consistent with this depletion occurring in the mid-Proterozoic, though the precise age of this event is poorly defined. Thus, when sampled by the Devonian Sloan kimberlite, the compositional characteristics of the lithospheric mantle in this area primarily reflected the initial melt extraction event that presumably is associated with crust formation in the Proterozoic-a relatively simple history that may also explain the cold geotherm measured for the Sloan xenoliths. The Williams and Homestead kimberlites erupted through the Wyoming Craton in the Eocene, near the end of the Laramide Orogeny, the major tectonomagmatic event responsible for the formation of the Rocky Mountains in the late Cretaceous-early Tertiary. Rhenium-depletion model ages for the Homestead peridotites are mostly Archean, consistent with their origin in the Archean lithospheric mantle of the Wyoming Craton. Both the Williams and Homestead peridotites, however, clearly show the consequences of metasomatism by incompatible-element-rich melts. Intermineral isotope systematics in both the Homestead and Williams peridotites are highly disturbed with the Sr and Nd isotopic compositions of the minerals being dominated by the metasomatic component. Some Homestead samples preserve an incompatible element depleted signature in their radiogenic Hf isotopic compositions. Sm-Nd tie lines for garnet and clinopyroxene separates from most Homestead samples provide Mesozoic or younger "ages" suggesting that the metasomatism occurred during the Laramide. Highly variable Rb-Sr and Lu-Hf mineral "ages" for these same samples suggest that the Homestead peridotites did not achieve intermineral equilibrium during this metasomatism. This indicates that the metasomatic overprint likely was introduced shortly before kimberlite eruption through interaction of the peridotites with the host kimberlite, or petrogenetically similar magmas, in the Wyoming Craton lithosphere. ?? 2004 Elsevier B.V. All rights reserved.

Core formation in the Moon: The mystery of the excess depletion of Mo, W and P

NASA Technical Reports Server (NTRS)

Newsom, H. E.; Maehr, S. A.

1993-01-01

We have evaluated siderophile element depletion models for the Moon in light of our improved statistical treatment of siderophile element abundance data and new information on the physics of core formation. If core formation occurred in the Moon at the large degrees of partial melting necessary for metal segregation, according to recent estimates, then a significant inconsistency (not seen in the eucrite parent body) exists in the depletion of the incompatible siderophile elements Mo, W, and P, compared to other siderophile elements in the Moon. The siderophile data, with the exception of Mo, are most consistent with terrestrial initial siderophile abundances and segregation of a very small core in the Moon. Our improved abundance estimates and possible explanations for these discrepancies are discussed.

Distribution of potentially hazardous trace elements in coals from Shanxi province, China

USGS Publications Warehouse

Zhang, J.Y.; Zheng, C.G.; Ren, D.Y.; Chou, C.-L.; Liu, J.; Zeng, R.-S.; Wang, Z.P.; Zhao, F.H.; Ge, Y.T.

2004-01-01

Shanxi province, located in the center of China, is the biggest coal base of China. There are five coal-forming periods in Shanxi province: Late Carboniferous (Taiyuan Formation), Early Permian (Shanxi Formation), Middle Jurassic (Datong Formation), Tertiary (Taxigou Formation), and Quaternary. Hundred and ten coal samples and a peat sample from Shanxi province were collected and the contents of 20 potentially hazardous trace elements (PHTEs) (As, B, Ba, Cd, Cl, Co, Cr, Cu, F, Hg, Mn, Mo, Ni, Pb, Sb, Se, Th, U, V and Zn) in these samples were determined by instrumental neutron activation analysis, atomic absorption spectrometry, cold-vapor atomic absorption spectrometry, ion chromatography spectrometry, and wet chemical analysis. The result shows that the brown coals are enriched in As, Ba, Cd, Cr, Cu, F and Zn compared with the bituminous coals and anthracite, whereas the bituminous coals are enriched in B, Cl, Hg, and the anthracite is enriched in Cl, Hg, U and V. A comparison with world averages and crustal abundances (Clarke values) shows that the Quaternary peat is highly enriched in As and Mo, Tertiary brown coals are highly enriched in Cd, Middle Jurassic coals, Early Permian coals and Late Carboniferous coals are enriched in Hg. According to the coal ranks, the bituminous coals are highly enriched in Hg, whereas Cd, F and Th show low enrichments, and the anthracite is also highly enriched in Hg and low enrichment in Th. The concentrations of Cd, F, Hg and Th in Shanxi coals are more than world arithmetic means of concentrations for the corresponding elements. Comparing with the United States coals, Shanxi coals show higher concentrations of Cd, Hg, Pb, Se and Th. Most of Shanxi coals contain lower concentrations of PHTEs. ?? 2004 Elsevier Ltd. All rights reserved.

Time-Series Radiocarbon Measurements Indicate Carbon Turnover Across Soil Fractions is Correlated With Productivity in a Long-Term Agricultural Experiment

NASA Astrophysics Data System (ADS)

Sanderman, J.; Baisden, W. T.; Creamer, C.; Farrell, M.; Fallon, S.

2016-12-01

Carbonatites and alkaline intrusions are important sources of REEs. Environmental risks related to these deposit types have been assessed through literature review and evaluation of the geochemical properties of representative samples of mill tailings and their leachates. The main ore mineral in carbonatite deposits is bastnasite [(Ce,La)(CO3)F], which is found with dolomite and calcite ( 65 %), barite (20 - 25 %), plus a number of minor accessory minerals including sulfides such as galena and pyrite. Generally, alkaline intrusion-related REE deposits either occur in layered complexes or with dikes and veins cutting alkaline intrusions. Such intrusions have a more diverse group of REE ore minerals that include fluorcarbonates, oxides, silicates, and phosphates. Ore also can include minor calcite and iron (Fe), lead (Pb), and zinc (Zn) sulfides. The acid-generating potential of both deposit types is low because of a predominance of carbonate minerals in the carbonatite deposits, the presence of feldspars and minor calcite in alkaline intrusion-related deposits, and to only minor to trace occurrence of potentially acid-generating sulfide minerals. Both deposit types, however, are produced by igneous and hydrothermal processes that enrich high-field strength, incompatible elements, which typically are excluded from common rock-forming minerals. Elements such as yttrium (Y), niobium Nb), zirconium (Zr), hafnium (Hf), tungsten (W), titanium (Ti), tantalum (Ta), scandium (Sc), thorium (Th), and uranium (U) can be characteristic of these deposits and may be of environmental concern. Most of these elements, including the REEs, but with the exception of U, have low solubilities in water at the near-neutral pH values expected around these deposits. Mill tailings from carbonatite deposits can exceed residential soil and sediment criteria for Pb, and leachates from mill tailings can exceed drinking water guidelines for Pb. The greatest environmental challenges, however, are linked to the presence of Th and U, although mineral hosts for these elements are moderately unreactive in the environment. Both deposit types can have mill tailings that exceed residential soil criteria for U. Uranium can be recovered as a byproduct to mitigate its environmental effects, but Th remains a waste product that requires management.

Garnet lherzolites from Louwrensia, Namibia: Bulk composition and P/T relations

USGS Publications Warehouse

Boyd, F.R.; Pearson, D.G.; Hoal, Karin O.; Hoal, B.G.; Nixon, P.H.; Kingston, M.J.; Mertzman, S.A.

2004-01-01

Bulk, mineral and trace element analyses of garnet lherzolite xenoliths from the Louwrensia kimberlite pipe, south-central Namibia, together with previously published Re-Os isotopic data [Chem. Geol. (2004)], form the most extensive set of chemical data for off-craton suites from southern Africa. The Louwrensia suite is similar to those from the Kaapvaal craton in that it includes both predominantly coarse-grained, equant-textured peridotites characterised by equilibration temperatures 1200 ??C. Redepletion ages range back to 2.1 Gy, concordant with the age of the crustal basement and about 1 Gy younger than the older peridotites of the adjacent Kaapvaal craton root. The coarse, low-temperature Louwrensia peridotites have an average Mg number for olivine of 91.6 in comparison to 92.6 for low-temperature peridotites from the craton. Orthopyroxene content averages 24 wt.% with a range of 11-40 wt.% for Louwrensia low-temperature peridotites, in comparison to a mean of 31.5 wt.% and a range of 11-44 wt.% for low-temperature peridotites from the Kaapvaal craton. Other major, minor and trace element concentrations in minerals forming Louwrensia lherzolites are more similar to values in corresponding Kaapvaal peridotite minerals than to those in lithospheric peridotites of Phanerozoic age as represented by off-craton basalt-hosted xenoliths and orogenic peridotites. Proportions of clinopyroxene and garnet in both the Louwrensia and Kaapvaal lherzolites overlap in the range up to 10 wt.% forming a trend extending towards pyrolite composition. Disequilibrium element partitioning between clinopyroxene and garnet for some incompatible trace elements is evidence that some of the trend is caused by enrichment following depletion. The disequilibrium is interpreted to have been caused by relatively recent growth of diopside, as previously suggested for cratonic peridotites. Attempts to constrain the depth of melting required to produce the Louwrensia peridotites suggests formation at pressures 200 km). Temperature-depth plots for the high-temperature Louwrensia rocks, however, form pronounced, apparent higher-temperature thermal anomalies at depths of 140 km and above. These anomalies are believed to reflect regional igneous activity, perhaps associated with thermal erosion of an originally thicker lithosphere, a short time prior to eruption. ?? 2004 Elsevier B.V. All rights reserved.

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.

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

Kent, A.J.R.; Clague, D.A.; Honda, M.

Many tholeiitic and transitional pillow-rim and fragmental glasses from Loihi seamount, Hawaii, have high Cl contents and Cl/K{sub 2}O ratios (and ratios of Cl to other incompatible components, such as P{sub 2}O{sub 5}, H{sub 2}O, etc.) relative to other Hawaiian subaerial volcanoes (e.g., Mauna Loa, Mauna Kea, and Kilauea). The authors suggest that this results from widespread contamination of Loihi magmas by a Cl-rich, seawater-derived component. Assimilation of high-Cl phases such as saline brine or Cl-rich minerals (halite or iron-hydroxychlorides) with high Cl/H{sub 2}O ratios can explain the range and magnitude of Cl contents in Loihi glasses, as well asmore » the variations in the ratios of Cl to other incompatible elements. Brines and Cl-rich minerals are thought to form from seawater within the hydrothermal systems associated with submarine volcanoes, and Loihi magmas could plausibly have assimilated such materials from the hydrothermal envelope adjacent to the magma chamber. Their model can also explain semiquantitatively the observed contamination of Loihi glasses with atmospheric-derived noble gases, provided the assimilant has concentrations of Ne and Ar comparable to or slightly less than seawater. This is more likely for brines than for Cl-rich minerals, leading the authors to favor brines as the major assimilant. Cl/Br ratios for a limited number of Loihi samples are also seawater-like, and show no indication of the higher values expected to be associated with the assimilation of Cl-rich hydrothermal minerals. Although Cl enrichment is a common feature of lavas from Loihi, submarine glasses from other Hawaiian volcanoes show little (Kilauea) or no (Mauna Loa, Mauna Kea) evidence of this process, suggesting that assimilation of seawater-derived components is more likely to occur in the early stages of growth of oceanic volcanoes. Summit collapse events such as the one observed at Loihi in October 1996 provide a ready mechanism for depositing brine-bearing rocks from the volcanic edifice into the top of a submarine summit magma chamber.« less

Cryogenic propellant management: Integration of design, performance and operational requirements

NASA Technical Reports Server (NTRS)

Worlund, A. L.; Jamieson, J. R., Jr.; Cole, T. W.; Lak, T. I.

1985-01-01

The integration of the design features of the Shuttle elements into a cryogenic propellant management system is described. The implementation and verification of the design/operational changes resulting from design deficiencies and/or element incompatibilities encountered subsequent to the critical design reviews are emphasized. Major topics include: subsystem designs to provide liquid oxygen (LO2) tank pressure stabilization, LO2 facility vent for ice prevention, liquid hydrogen (LH2) feedline high point bleed, pogo suppression on the Space Shuttle Main Engine (SSME), LO2 low level cutoff, Orbiter/engine propellant dump, and LO2 main feedline helium injection for geyser prevention.

Trace-metal concentrations in African dust: effects of long-distance transport and implications for human health

USGS Publications Warehouse

Garrison, Virginia; Lamothe, Paul; Morman, Suzette; Plumlee, Geoffrey S.; Gilkes, Robert; Prakongkep, Nattaporn

2010-01-01

The Sahara and Sahel lose billions of tons of eroded mineral soils annually to the Americas and Caribbean, Europe and Asia via atmospheric transport. African dust was collected from a dust source region (Mali, West Africa) and from downwind sites in the Caribbean [Trinidad-Tobago (TT) and U.S. Virgin Islands (VI)] and analysed for 32 trace-elements. Elemental composition of African dust samples was similar to that of average upper continental crust (UCC), with some enrichment or depletion of specific trace-elements. Pb enrichment was observed only in dust and dry deposition samples from the source region and was most likely from local use of leaded gasoline. Dust particles transported long-distances (VI and TT) exhibited increased enrichment of Mo and minor depletion of other elements relative to source region samples. This suggests that processes occurring during long-distance transport of dust produce enrichment/depletion of specific elements. Bioaccessibility of trace-metals in samples was tested in simulated human fluids (gastric and lung) and was found to be greater in downwind than source region samples, for some metals (e.g., As). The large surface to volume ratio of the dust particles (<2.5 µm) at downwind sites may be a factor.

Elemental and Isotopic Tomography at Single-Atom-Scale in 4.0 and 2.4 Ga Zircons

NASA Astrophysics Data System (ADS)

Valley, J. W.; Reinhard, D. A.; Snoeyenbos, D.; Lawrence, D.; Martin, I.; Kelly, T. F.; Ushikubo, T.; Strickland, A.; Cavosie, A. J.

2012-12-01

Atom probe tomography can determine identity (mass/charge ratio) and 3-D position of individual atoms in minerals such as zircon. These data provide unique information for understanding the thermal history and mechanisms of mineral reaction and exchange, including radiation damage. Nine needle-shaped specimens ~100 nm in diameter (at the apex) were sampled from 2 zircons by FIB and analyzed with a local-electrode atom probe (LEAP), CAMECA LEAP 4000X HR. The LEAP uses pulsed-laser heating to field evaporate the tip of a zircon needle and accelerates the ions into a position-sensitive TOF-MS. With due care for complex isobaric interferences (molecules, multiple ionizations) and background correction, it is possible to individually identify up to 10E8 atoms/needle (36% detection efficiency) by mass/charge (MRP ~ 1000@ m/n=16Da) and position (X-Y-Z coordinates on 0.2 nm scale) (Kelly & Larson 2012). The 3-D distribution of Pb and Y differ at atom-scale in the 2 zircons. Zircon #1 (4007 Ma, Jack Hills, W. Australia, Cavosie 2005, Ushikubo et al. 2008, Bouvier et al. 2011) is homogeneous in Pb and Y. In contrast, incompatible elements, including Pb and Y, are concentrated in equant 5-10 nm dia. domains, spaced ~50 nm apart in zircon #2 (2438 Ma, Albion-Raft R-Grouse Ck core complex, Utah, Strickland et al. 2011). U is homogeneously distributed in both zircons. The analyzed domains suffered 4-8 x 10E15 α-decay events/mg due to U and Th decay and yet both zircons yield >97% concordant U-Pb ages by SIMS, suggesting annealing of radiation damage during the life of the zircons. The 207-Pb/206-Pb ratios for these nm-scale domains, as measured by LEAP, average 0.17 for the 2.4 Ga Zrc2 (3 needles) and 0.43 for the 4.0 Ga Zrc1 (5 needles). These ratios are less precise (±40% 2σ) due to ultra-small sample size, but are in excellent agreement with values measured by SIMS, 0.1684 and 0.4269, respectively. Thus Pb in both zircons is radiogenic. The Pb-Y-rich domains and lack of correlation with U in Zrc2 is best explained by diffusion of Pb and other incompatible elements (Y, REEs) into 5-10 nm domains that were damaged by α-recoil and may have been metamict as the result of single U- or Th-decay chains. Diffusion distances of ~20 nm for these elements in crystalline zircon require temperatures above 700 C for ~10 myrs (Cherniak 2010). This is consistent with the known history of Zrc2, as a xenocrystic 2.4 Ga zircon in a 29 Ma granodiorite phase of a long-lived, extension-related plutonic suite that experienced high-grade regional metamorphism. In contrast, the absence of enriched domains in Zrc1 suggests that this zircon did not experience similar high-grade metamorphism before or after its deposition within the ~3 Ga Jack Hills metaconglomerate.

Melt inclusion evidence for the relative timing of assimilation and crystallisation in high MgO lavas, Mull, Scotland

NASA Astrophysics Data System (ADS)

Peate, D. W.; Ukstins Peate, I.; Rowe, M. C.; Thompson, J. M.; Kerr, A. C.

2010-12-01

Whole rock data on the Mull Plateau Group lavas (Scotland) show that the most primitive lavas (MgO >8 wt%) are the most crustally contaminated. One model is that hot, high-MgO magmas flow turbulently during ascent allowing more assimilation to occur than in the laminar flow regime expected for cooler, more viscous, lower-MgO magmas. We present data on rehomogenized olivine-hosted melt inclusions from four representative high-MgO flows to investigate the nature of the assimilation process in more detail. One complication on Mull is the potential effect of pervasive hydrothermal metamorphism on whole rock compositions. Melt inclusions are more protected against alteration effects within their host olivine crystal, and potentially allow more robust estimates of magmatic liquid compositions. Low sulphur contents were used to screen for degassed / breached inclusions, and the compositions of unbreached inclusions were corrected for post-entrapment crystallisation and Fe-loss. The four whole rock samples show a limited variation in Na2O (2.4-2.8 wt%) and K2O (0.23-0.29 wt%) despite a wide range in immobile element contents (e.g. Zr 62-126 ppm, Nb 2.4-4.6 ppm). In contrast, the melt inclusions show a far greater variability in Na2O (1.8-4.0 wt%) and K2O (0.02-0.35 wt%) and coherent positive correlations between K and Na. Melt inclusions from different samples show systematic correlations between alkalis (K+Na) and incompatible element ratios such as Zr/Y and La/Sm, indicating that the melt inclusions are recording magmatic values for fluid mobile elements such as K and Na. For the two most incompatible element enriched samples, the whole rock analysis is similar to the melt inclusions except for lower Na and higher Ba that are related to alteration. Therefore, any crustal assimilation in these magmas must have take place prior to the growth of the olivines in the samples. For the two more depleted samples, the melt inclusions have less contaminated compositions than the whole rocks, and also show broad trends of increasing K/Ti (extent of assimilation) with decreasing Fo% of the host olivine (extent of differentiation). For these samples, significant crustal assimilation must have taken place both during and after growth of the olivines in the samples. Melt inclusions from individual samples show limited variability in Zr/Y compared with K/Ti, indicating that aggregation of melts from different parts of the melting column must have occurred at deeper levels prior to growth of the olivines in the samples. Reconnaissance H2O and CO2 analyses by SIMS allow estimates to be made of minimum inclusion entrapment depths of at least 3 to 7 km. Although it is apparent that whole rock compositional variations still capture the broad details of crustal assimilation and melting histories for Mull lavas despite the variable effects of hydrothermal alteration, we demonstrate that melt inclusion data can more clearly resolve details of these magmatic processes.

Carboniferous high-pressure metamorphism of Ordovician protoliths in the Argentera Massif (Italy), Southern European Variscan belt

NASA Astrophysics Data System (ADS)

Rubatto, Daniela; Ferrando, Simona; Compagnoni, Roberto; Lombardo, Bruno

2010-04-01

The age of high-pressure metamorphism is crucial to identify a suitable tectonic model for the vast Variscan orogeny. Banded H P granulites from the Gesso-Stura Terrain in the Argentera Massif, Italy, have been recently described (Ferrando et al., 2008) relicts of high-pressure metamorphism in the western part of the Variscan orogen. Bulk rock chemistry of representative lithologies reveals intermediate silica contents and calc-alkaline affinity of the various cumulate layers. Enrichment in incompatible elements denotes a significant crustal component in line with intrusion during Ordovician rifting. Magmatic zircon cores from a Pl-rich layer yield scattered ages indicating a minimum protolith age of 486 ± 7 Ma. Carboniferous zircons (340.7 ± 4.2 and 336.3 ± 4.1 Ma) are found in a Pl-rich and a Pl-poor layer, respectively. Their zoning, chemical composition (low Th/U, flat HREE pattern and Ti-in-zircon temperature) and deformation indicate that they formed during the high-pressure event before decompression and mylonitisation. The proposed age for high-pressure metamorphism in the Argentera Massif proves that subduction preceded anatexis by less than 20 Ma. The new data allow a first-order comparison with the Bohemian Massif, which is located at the eastern termination of the Variscan orogen. Similarities in evolution at either end of the orogen support a Himalayan-type tectonic model for the entire European Variscides.

Atom Probe Tomography of Phase and Grain Boundaries in Experimentally-Deformed and Hot-Pressed Wehrlite

NASA Astrophysics Data System (ADS)

Cukjati, J.; Parman, S. W.; Cooper, R. F.; Zhao, N.

2017-12-01

Atom probe tomography (APT) was used to characterize the chemistry of three grain boundaries: an olivine-olivine (ol-ol) and olivine-clinopyroxene (ol-cpx) boundary in fine-grained experimentally-deformed wehrlite and an ol-cpx boundary in a fine-grained, hot-pressed wehrlite. Grain boundaries were extracted and formed into APT tips using a focused ion beam (FIB). The tips were analyzed in a reflectron-equipped LEAP4000HR (Harvard University) at 1% or 0.5% detection rate, 5pJ laser energy and 100kHz pulse rate. Total ion counts are between 40 and 100 million per tip. Examination of grain and phase boundaries in wehrlite are of interest since slow-diffusing and olivine-incompatible cations present in cpx (e.g. Ca and Al) may control diffusion-accommodated grain boundary sliding and affect mantle rheology (Sundberg & Cooper, 2008). At steady state, ol-cpx aggregates are weaker than either ol or cpx end member, the results of which are not currently well-explained. We investigate grain boundary widths to understand the transport of olivine-incompatible elements. Widths of grain/phase boundary chemical segregation are between 3nm and 6nm for deformed ol-ol and ol-cpx samples; minimally-deformed (hot-pressed) samples having slightly wider chemical segregation widths. Chemical segregation widths were determined from profiles of Na, Al, P, Cl, K, Ca, or Ni, although not all listed elements can be used for all samples (e.g. Na, K segregation profiles can only be observed for ol-ol sample). These estimates are consistent with prior estimates of grain boundary segregation by atom probe tomography on ol-ol and opx-opx samples (Bachhav et al., 2015) and are less than ol-ol interface widths analyzed by STEM/EDX (Hiraga, Anderson, & Kohlstedt, 2007). STEM/EDX will be performed on deformed wehrlite to investigate chemical profile as a function of applied stress orientation and at length scales between those observable by APT and EPMA. Determination of phase boundary chemistry and structure allows for better modeling of the rheology of multiphase aggregates and better understanding of diffusive transport and storage of incompatible elements along grain boundaries.

Fluid fractionation of tungsten during granite-pegmatite differentiation and the metal source of peribatholitic W quartz veins: Evidence from the Karagwe-Ankole Belt (Rwanda)

NASA Astrophysics Data System (ADS)

Hulsbosch, Niels; Boiron, Marie-Christine; Dewaele, Stijn; Muchez, Philippe

2016-02-01

The identification of a magmatic source for granite-associated rare metal (W, Nb, Ta and Sn) mineralisation in metasediment-hosted quartz veins is often obscured by intense fluid-rock interactions which metamorphically overprinted most source signatures in the vein system. In order to address this recurrent metal sourcing problem, we have studied the metasediment-hosted tungsten-bearing quartz veins of the Nyakabingo deposit of the Karagwe-Ankole belt in Central Rwanda. The vein system (992 ± 2 Ma) is spatiotemporal related to the well-characterised B-rich, F-poor G4 leucogranite-pegmatite suite (986 ± 10 Ma to 975 ± 8 Ma) of the Gatumba-Gitarama area which culminated in Nb-Ta-Sn mineralisation. Muscovite in the Nyakabingo veins is significantly enriched in granitophile elements (Rb, Cs, W and Sn) and show alkali metal signatures equivalent to muscovite of less-differentiated pegmatite zones of the Gatumba-Gitarama area. Pegmatitic muscovite records a decrease in W content with increasing differentiation proxies (Rb and Cs), in contrast to the continuous enrichment of other high field strength elements (Nb and Ta) and Sn. This is an indication of a selective redistribution for W by fluid exsolution and fluid fractionation. Primary fluid inclusions in tourmaline of these less-differentiated pegmatites demonstrate the presence of medium to low saline, H2O-NaCl-KCl-MgCl2-complex salt (e.g. Rb, Cs) fluids which started to exsolve at the G4 granite-pegmatite transition stage. Laser ablation inductively coupled plasma mass-spectrometry shows significant tungsten enrichment in these fluid phases (∼5-500 ppm). Fractional crystallisation has been identified previously as the driving mechanism for the transition from G4 granites, less-differentiated biotite, biotite-muscovite towards muscovite pegmatites and eventually columbite-tantalite mineralised pegmatites. The general absence of tungsten mineralisation in this magmatic suite, including the most differentiated columbite-tantalite mineralised pegmatites of the Gatumba-Gitarama area, emphasises the efficiency of fluid saturation to extract crystal-melt incompatible tungsten from the differentiating melt phase. Fluid-melt-crystal partitioning calculations support the concept of a magmatic-hydrothermal fluid source for tungsten and constrain the range of permissible crystal-melt and fluid-melt partition coefficients together with realistic values for water solubility in the parental G4 granitic melt. Consequently, we propose that for highly-differentiated B-rich, F-poor granite systems fluid saturation started prior to or at the granite-pegmatite transition stage resulting in apical to peribatholitic tungsten veins systems that are paragenetically older than the final pegmatite stage.

Undegassed Carbon Content from a Highly Depleted Segment of the Mid-Atlantic Ridge (1-5°S): Evidence from Melt Inclusions

NASA Astrophysics Data System (ADS)

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

2014-12-01

As carbon solubility is low in basalts, MORB contain little dissolved CO2 (189±61 ppm, 1σ, n=600 [1]). A global negative correlation between CO2/Nb (proxy for amount of CO2 lost by degassing) and Ba/La (proxy for source enrichment) indicates that depleted MORB are less affected by degassing than enriched MORB: CO2/Nb ratios range from 0-100 for samples with Ba/La>4, while CO2/Nb range from 50 to 400 for samples with Ba/La<4 [1]. To assess the CO2 content of undegassed MORB, we analyzed the volatile content of 70 olivine-hosted, glassy melt inclusions (MIs) from four basalts dredged along MAR 1-5°S, a ridge segment that produces highly depleted MORB in terms of trace element enrichment and radiogenic isotopes [2, 3]. MIs contain CO2 contents (180-1420 ppm) that are higher than their respective matrix glasses (130-220 ppm, typical for vapor-saturated melts erupted at 3-5 km b.s.l.). One of the four dredges (EN061 5D-3Ag) contains MIs that do not exhibit shrinkage bubbles. For this sample only, we find a positive correlation between the CO2 content (240-770 ppm) and the Cl content (6-20 ppm) of the MIs that is not found in the matrix glasses (see Fig.). We infer that the correlation between CO2 and Cl, both highly incompatible in silicate minerals during fractional crystallization, is strong evidence for vapor-undersaturation, as any CO2 degassing would have erased the correlation. Together with MIs from the Siqueiros Fracture Zone [4] and from northern Iceland [5], the MIs from EN061 5D-3Ag may represent another occurrence of carbon-undersaturated MORB. Our results will be used to model the primary carbon content of MORB and of the depleted upper mantle. Note that the average Cl content of the matrix glasses (20±1 ppm) is higher than those of the MIs (12±3 ppm, see Fig.). This indicates either that the matrix glasses assimilated a small amount of seawater Cl, or that the MIs are all more depleted than the matrix glass. We will acquire major and trace element data in order to further investigate the origin of the low Cl and high CO2 contents in these MIs. Ref. [1] Le Voyer et al. 2014 Goldschmidt abstr. [2] Schilling et al. 1994 JGR 99 [3] Kelley et al. 2013 G3 [4] Saal et al. 2002 Nature 419 [5] Hauri and Saal 2009 EOS Fall suppl. AGU abstr.

The chemical signatures of progressive dehydration stages in subducted serpentinites

NASA Astrophysics Data System (ADS)

Pettke, T.; Spandler, C.; Kodolanyi, J.; Scambelluri, M.

2009-04-01

Fluids mediate chemical cycling in subduction zones. Nonetheless, the chemistry of serpentinite-dehydration fluids from down-going slabs and their chemical effects on ascent are only very poorly constrained. We report new data on discontinuous dehydration reactions, including the measurement of individual fluid inclusions in prograde minerals from natural occurrences, and one case study tracing the infiltration of serpentinite-derived fluid in mafic eclogite. Together, these studies demonstrate that serpentinite-derived fluids are commonly dilute, but that there may be selected trace element abundances (and ratios ?) that characterize such fluid provenance. Brucite dehydration represents the first relevant liberation of crystal-bound water from serpentinites formed on the ocean floor (ocean floor mantle hydration chemistry is addressed in Kodolanyi et al., this session). Discordant olivine-Ti-clinohumite-antigorite-clinopyroxene-magnetite veins in ca. 2.3 GPa antigorite serpentinites of the Erro Tobbio in the Ligurian Alps, Italy, formed from aqueous, dilute fluids containing Li, Sr, Ba, Rb, Pb as determined on texturally-early fluid inclusions in olivine. This prograde olivine preserves high Ni (1500 - 3000 µg/g) and is identified most readily by elevated Li (1-20 µg/g), B (1-20 µg/g) and Mn contents. Aqueous fluid inclusions in some clinopyroxene (Cpx) of the same veins host variably (sometimes highly) saline fluid inclusions, interpreted to represent the "spent" fluid after formation of hydrous vein minerals (chlorite, antigorite). Vein bulk-rock trace-element concentrations show enrichment in Ti, Ba, Nb, Li, HREE and Cu relative to the wall rocks, accompanied by depletion in Cr. This mostly reflects the mineral transformations (sources / sinks) occurring at this stage of serpentinite dehydration. Antigorite-breakdown is arguably the most prominent water release from down-going slabs. Olivine-orthopyroxene-chlorite rocks at Cerro del Almirez (Spain), recording this dehydration event, contain olivine-hosted polyphase inclusions interpreted to represent fluid inclusions trapped during antigorite breakdown. Preliminary compositional data show enrichments in B, Cs, Pb, Li, Sr, Rb, K, Ba (decreasing order) and depletions in Ca, Ti, La relative to primitive mantle, closely corresponding to the incompatible element pattern of typical island arc lavas. Transfer of such fluids to the melting source of island arc magmas may be critical to developing their distinctive trace element signatures. Omphacite-rich (± garnet, rutile, talc and zircon) veins cutting eclogite (Fe-Ti gabbro protolith, Monviso, W Italian Alps) record serpentinite-derived fluid pathways though the subducted slab at ca. 70 km depth. Although these veins largely formed by local eclogite-derived fluids, they also preserve discrete generations of vein minerals enriched in Mg, Cr, Ni, B, As and Sb, and zircon with elevated Epsilon(Hf) compared to host-rock eclogite zircon. These chemical and isotopic characteristics suggest external fluid input, from serpentinite dehydration. Moreover, distinctive oscillatory or irregular Cr zonations observed in omphacite, garnet and rutile from the veins are interpreted to record episodic fracturing and fluid infiltration over >10 m along transient brittle fractures at high pressures. Our current data suggest that dehydration fluid pervades the rock at the site of liberation, and that episodic fluid escape from the dehydration site may be effectively channelized. This supports growing evidence for highly focused reactive fluid flow through slabs. Robust constraints on the chemical composition and nature of dehydration fluids from serpentinites and how they evolve during ascent may greatly aid in recognizing such features from outcrop to thin-section scales, in turn providing us with more comprehensive sample material to advance our understanding on fluid-mediated cycling in subduction zones. Reference Kodolanyi et al., this session

Hf-Nd Isotopes in West Philippine Basin Basalts: Results from International Ocean Discovery Program (IODP) Site U1438 and Implications for the Early History of the Izu-Bonin-Mariana (IBM) Subduction System

NASA Astrophysics Data System (ADS)

Yogodzinski, G. M.; Hocking, B.; Bizimis, M.; Hickey-Vargas, R.; Ishizuka, O.; Bogus, K.; Arculus, R. J.

2015-12-01

Drilling at IODP Site U1438, located immediately west of Kyushu-Palau Ridge (KPR), the site of IBM subduction initiation, penetrated 1460 m of volcaniclastic sedimentary rock and 150 m of underlying basement. Biostratigraphic controls indicate a probable age for the oldest sedimentary rocks at around 55 Ma (51-64 Ma - Arculus et al., Nat Geosci in-press). This is close to the 48-52 Ma time period of IBM subduction initiation, based on studies in the forearc. There, the first products of volcanism are tholeiitic basalts termed FAB (forearc basalt), which are more depleted than average MORB and show subtle indicators of subduction geochemical enrichment (Reagan et al., 2010 - Geochem Geophy Geosy). Shipboard data indicate that Site U1438 basement basalts share many characteristics with FABs, including primitive major elements (high MgO/FeO*) and strongly depleted incompatible element patterns (Ti, Zr, Ti/V and Zr/Y below those of average MORB). Initial results thus indicate that FAB geochemistry may have been produced not only in the forearc, but also in backarc locations (west of the KPR) at the time of subduction initiation. Hf-Nd isotopes for Site 1438 basement basalts show a significant range of compositions from ɛNd of 7.0 to 9.5 and ɛHf of 14.5 to 19.8 (present-day values). The data define a well-correlated and steep array in Hf-Nd isotope space. Relatively radiogenic Hf compared to Nd indicates an Indian Ocean-type MORB source, but the dominant signature, with ɛHf >16.5, is more radiogenic than most Indian MORB. The pattern through time is from more-to-less radiogenic and more variable Hf-Nd isotopes within the basement section. This pattern culminates in basaltic andesite sills, which intrude the lower parts of the sedimentary section. The sills have the least radiogenic compositions measured so far (ɛNd ~6.6, ɛHf ~13.8), and are similar to those of boninites of the IBM forearc and modern IBM arc and reararc rocks. The pattern within the basement suggests modest enrichment of a depleted Indian MORB source over time.

Geochemistry and petrology of andesites from the north rift zone of Axial Seamount, Juan de Fuca Ridge

NASA Astrophysics Data System (ADS)

Smithka, I. N.; Perfit, M. R.; Clague, D. A.; Wanless, V. D.

2014-12-01

In 2013, the ROV Doc Ricketts onboard R/V Western Flyer explored ~4 km of an elongate pillow ridge up to ~300 m high along the eastern edge of the north rift zone of Axial Seamount. The steep-sided volcanic ridge is constructed of large pillow lavas up to 2-3 m in diameter and smaller elongated pillow tubes. Of the 27 samples collected during dive D526, all but one are andesites making it one of the largest confirmed high-silica exposures along a mid-ocean ridge (MOR). Based on radiocarbon ages of sediment on top of flows, the mounds are at least ~1390 years old. This minimum age is much younger than the 56 Ka age calculated based on distance from the rift axis, indicating eruption off-axis through older, colder crust and supporting the hypothesis and model calculations that extensive fractional crystallization (>85%) caused the high silica content. The andesitic lavas are primarily glassy, highly vesicular, crusty, and sparsely phyric with small (~1 mm) plagioclase crystals and olivine, clinopyroxene, and Fe-Ti oxide microphenocrysts. Microprobe analyses of glasses are similar to wax-core samples previously collected from this area but are more compositionally variable. Excluding one basalt (7.7 wt% MgO) sampled between mounds, the lavas are basaltic andesites and andesites (53-59 wt% SiO2) with <3 wt% MgO and 12.8-15.7 wt% FeO concentrations. Incompatible trace element abundances are ~4-6 times more enriched than in Axial Seamount T-MORB. Primitive mantle-normalized patterns are similar to those of high-silica lavas from other MORs (southern Juan de Fuca Ridge, 9N East Pacific Rise) with significant positive U anomalies, large negative Sr anomalies, small negative Eu anomalies, and slight positive Zr-Hf anomalies. The andesites are more enriched in light rare earth elements than basalts from Axial Seamount ((La/Yb)N 1.35-1.4 vs. 0.7-1.27) and N-MORB from the southern Juan de Fuca Ridge. The andesites also have high Cl (~0.3-0.6 wt%) and H2O (~1.60-1.71 wt%) contents; common features of other high-silica MOR suites and indicative that some assimilation of altered crust was involved in their petrogenesis.

Earth's evolving subcontinental lithospheric mantle: inferences from LIP continental flood basalt geochemistry

NASA Astrophysics Data System (ADS)

Greenough, John D.; McDivitt, Jordan A.

2018-04-01

Archean and Proterozoic subcontinental lithospheric mantle (SLM) is compared using 83 similarly incompatible element ratios (SIER; minimally affected by % melting or differentiation, e.g., Rb/Ba, Nb/Pb, Ti/Y) for >3700 basalts from ten continental flood basalt (CFB) provinces representing nine large igneous provinces (LIPs). Nine transition metals (TM; Fe, Mn, Sc, V, Cr, Co, Ni, Cu, Zn) in 102 primitive basalts (Mg# = 0.69-0.72) from nine provinces yield additional SLM information. An iterative evaluation of SIER values indicates that, regardless of age, CFB transecting Archean lithosphere are enriched in Rb, K, Pb, Th and heavy REE(?); whereas P, Ti, Nb, Ta and light REE(?) are higher in Proterozoic-and-younger SLM sources. This suggests efficient transfer of alkali metals and Pb to the continental lithosphere perhaps in association with melting of subducted ocean floor to form Archean tonalite-trondhjemite-granodiorite terranes. Titanium, Nb and Ta were not efficiently transferred, perhaps due to the stabilization of oxide phases (e.g., rutile or ilmenite) in down-going Archean slabs. CFB transecting Archean lithosphere have EM1-like SIER that are more extreme than seen in oceanic island basalts (OIB) suggesting an Archean SLM origin for OIB-enriched mantle 1 (EM1). In contrast, OIB high U/Pb (HIMU) sources have more extreme SIER than seen in CFB provinces. HIMU may represent subduction-processed ocean floor recycled directly to the convecting mantle, but to avoid convective homogenization and produce its unique Pb isotopic signature may require long-term isolation and incubation in SLM. Based on all TM, CFB transecting Proterozoic lithosphere are distinct from those cutting Archean lithosphere. There is a tendency for lower Sc, Cr, Ni and Cu, and higher Zn, in the sources for Archean-cutting CFB and EM1 OIB, than Proterozoic-cutting CFB and HIMU OIB. All CFB have SiO2 (pressure proxy)-Nb/Y (% melting proxy) relationships supporting low pressure, high % melting resembling OIB tholeiites, but TM concentrations do not correlate with % melting. Thus, the association of layered intrusion (plutonic CFB) TM deposits with Archean terranes does not appear related to higher metal concentrations or higher percentages of melting in Archean SLM. Other characteristics of these EM1-like magmas (e.g., S2 or O2 fugacity) may lead to element scavenging and concentration during differentiation to form ore deposits.

3D hierarchical interface-enriched finite element method: Implementation and applications

NASA Astrophysics Data System (ADS)

Soghrati, Soheil; Ahmadian, Hossein

2015-10-01

A hierarchical interface-enriched finite element method (HIFEM) is proposed for the mesh-independent treatment of 3D problems with intricate morphologies. The HIFEM implements a recursive algorithm for creating enrichment functions that capture gradient discontinuities in nonconforming finite elements cut by arbitrary number and configuration of materials interfaces. The method enables the mesh-independent simulation of multiphase problems with materials interfaces that are in close proximity or contact while providing a straightforward general approach for evaluating the enrichments. In this manuscript, we present a detailed discussion on the implementation issues and required computational geometry considerations associated with the HIFEM approximation of thermal and mechanical responses of 3D problems. A convergence study is provided to investigate the accuracy and convergence rate of the HIFEM and compare them with standard FEM benchmark solutions. We will also demonstrate the application of this mesh-independent method for simulating the thermal and mechanical responses of two composite materials systems with complex microstructures.

Granulite-facies rocks in the Whatley Mill gneiss, Pine Mountain basement massif, Eastern Alabama

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

Daniell, N.; Salpas, P.A.

1993-03-01

The Pine Mountain basement massif is a granulite terrane exposed in a tectonic window through the Inner Piedmont of western Georgia and eastern Alabama. Investigations of the westernmost extent of the massif, the Whatley Mill Gneiss, have revealed four distinct lithologies: (1) an augen gneiss, the type lithology; (2) mylonite that develops in the shear zones cutting the unit; (3) a phaneritic rock showing weak to no foliation; (4) enclaves of biotite gneiss within the weakly-foliated rock. Additionally, the weakly-foliated rock comprises two distinct phases which are in sharp contact along curved and undulating boundaries: phase 1 is a coarser-grainedmore » rock; phase 2 is a finer-grained rock of the same mineralogy as phase 1 except it contains rare hypersthene. This first recorded observation of hypersthene unequivocally confirms the granulite-facies origin of the unit. Major and trace element compositions of the phase 1 rock are identical to those of the augen gneiss. The phase 2 rock, has a distinct composition with higher SiO[sub 2] and lower incompatible trace elements than the phase 1 rock. The enclaves display a range in major elements but higher incompatible elements than the other lithologies. Geochemical and petrologic relationships leads one to interpret: (1) the weakly-foliated rock retains many of its primary igneous features including its two phases and enclaves; (2) the two phases of the weakly-foliated rock arose as a result of injection of one magma (phase 2) into a cooler, crystal mush solidifying from another magma (phase 1); (3) the enclaves represent either autoliths of xenoliths; (4) the augen gneiss arose by isochemical deformation of the phase 1 rock.« less

Recent volcanism in the Siqueiros transform fault: Picritic basalts and implications for MORB magma genesis

USGS Publications Warehouse

Perfit, M.R.; Fornari, D.J.; Ridley, W.I.; Kirk, P.D.; Casey, J.; Kastens, K.A.; Reynolds, J.R.; Edwards, M.; Desonie, D.; Shuster, R.; Paradis, S.

1996-01-01

Small constructional volcanic landforms and very fresh-looking lava flows are present along one of the inferred active strike-slip faults that connect two small spreading centers (A and B) in the western portion of the Siqueiros transform domain. The most primitive lavas (picritic and olivine-phyric basalts), exclusively recovered from the young-looking flows within the A-B strike-slip fault, contain millimeter-sized olivine phenocrysts (up to 20 modal%) that have a limited compositional range (Fo91.5-Fo89.5) and complexly zoned Cr-Al spinels. High-MgO (9.5-10.6 wt%) glasses sampled from the young lava flows contain 1-7% olivine phenocrysts (Fo90.5-Fo89) that could have formed by equilibrium crystallization from basaltic melts with Mg# values between 71 and 74. These high MgO (and high Al2O3) glasses may be near-primary melts from incompatible-element depleted oceanic mantle and little modified by crustal mixing and/or fractionation processes. Phase chemistry and major element systematics indicate that the picritic basalts are not primary liquids and formed by the accumulation of olivine and minor spinel from high-MgO melts (10% < MgO < 14%). Compared to typical N-MORB from the East Pacific Rise, the Siqueiros lavas are more primitive and depleted in incompatible elements. Phase equilibria calculations and comparisons with experimental data and trace element modeling support this hypothesis. They indicate such primary mid-ocean ridge basalt magmas formed by 10-18% accumulative decompression melting in the spinel peridotite field (but small amounts of melting in the garnet peridotite field are not precluded). The compositional variations of the primitive magmas may result from the accumulation of different small batch melt fractions from a polybaric melting column.

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.

Enrichment and Bioavailability of Trace Elements in Soil in Vicinity of Railways in Japan.

PubMed

Wang, Zhen; Watanabe, Izumi; Ozaki, Hirozaku; Zhang, Jianqiang

2018-01-01

This study focuses on the concentrations, distribution, pollution levels, and bioavailability of 12 trace elements in soils along 6 different railways in Japan. Three diesel powered railways and three electricity powered railways were chosen as target. Surface soils (< 3 cm) were collected in vicinity of railways for analysis. Digestion and extraction were performed before concentration and bioavailability analysis. Enrichment factor was applied to investigate contamination levels of selected elements. The mean concentrations of Cr, Co, Ni, Cu, Zn, Sn, and Pb in soil samples were higher than soil background value in Japan. Concentrations of trace elements in soils along different railway had different characteristics. Horizontal distribution of Cu, Zn, Cd, Sn, and Pb in soil samples showed obviously downtrend with distance along railways with high frequency. Concentrations of V, Mn, Fe, and Co were higher in soils along railways which pass through city center. According to principal component analysis and cluster analysis, concentrations of Cu, Zn, Sn, and Pb could be considered as the indicators of soil contamination level along electricity powered trains, whereas indicators along diesel powered trains were not clear. Enrichment factor analysis proved that operation of freight trains had impact on pollution level of Cr, Ni, and Cd. Bioavailability of Mn, Co, Zn, and Cd in soil along electricity-powered railways were higher, and bioavailability of Pb in railways located in countryside was lower. Thus, enrichment and bioavailability of trace elements can be indicators of railway-originated trace elements pollution in soil.

Structure and Geochemistry of the Continental-Oceanic Crust Boundary of the Red Sea and the Rifted Margin of Western Arabia

NASA Astrophysics Data System (ADS)

Dilek, Y.; Furnes, H.; Schoenberg, R.

2009-12-01

The continental-oceanic crust boundary and an incipient oceanic crust of the Red Sea opening are exposed within the Arabian plate along a narrow zone of the Tihama Asir coastal plain in SW Saudi Arabia. Dike swarms, layered gabbros, granophyres and basalts of the 22 Ma Tihama Asir (TA) continental margin ophiolite represent products of magmatic differentiation formed during the initial stages of rifting between the African and Arabian plates. Nearly 4-km-wide zone of NW-trending sheeted dikes are the first products of mafic magmatism associated with incipient oceanic crust formation following the initial continental breakup. Gabbro intrusions are composed of cpx-ol-gabbro, cpx-gabbro, and norite/troctolite, and are crosscut by fine-grained basaltic dikes. Granophyre bodies intrude the sheeted dike swarms and are locally intrusive into the gabbros. Regional Bouger gravity anomalies suggest that the Miocene mafic crust represented by the TA complex extends westward beneath the coastal plain sedimentary rocks and the main trough of the Red Sea. The TA complex marks an incipient Red Sea oceanic crust that was accreted to the NE side of the newly formed continental rift in the earliest stages of seafloor spreading. Its basaltic to trachyandesitic lavas and dikes straddle the subalkaline-mildly alkaline boundary. Incompatible trace element relationships (e.g. Zr-Ti, Zr-P) indicate two distinct populations. The REE concentrations show an overall enrichment compared to N-MORB; light REEs are enriched over the heavy ones ((La/Yb)n > 1), pointing to an E-MORB influence. Nd-isotope data show ɛNd values ranging from +4 to +8, supporting an E-MORB melt source. The relatively large variations in ɛNd values also suggest various degrees of involvement of continental crust during ascent and emplacement, or by mixing of another mantle source.

Critical Elements in Fly Ash from the Combustion of Bituminous Coal in Major Polish Power Plants

NASA Astrophysics Data System (ADS)

Bielowicz, Barbara; Botor, Dariusz; Misiak, Jacek; Wagner, Marian

2018-03-01

The concentration of critical elements, including such REE as Fe, Co, W, Zn, Cr, Ni, V, Mn, Ti, Ag, Ga, Ta, Sr, Li, and Cu, in the so-called fly ash obtained from the 9 Polish power plants and 1 thermal power station has been determined. The obtained values, compared with the global average concentration in bituminous coal ash and sedimentary rocks (Clarke values), have shown that the enrichment of fly ash in the specified elements takes place in only a few bituminous coal processing sites in Poland. The enrichment factor (EF) is only slightly higher (the same order of magnitude) than the Clarke values. The enrichment factor in relation to the Clarke value in the Earth's crust reached values above 10 in all of the examined ashes for the following elements: Cr, Ni, V, W, and, in some ash samples, also Cu and Zn. The obtained values are low, only slightly higher than the global average concentrations in sedimentary rocks and bituminous coal ashes. The ferromagnetic grains (microspheres) found in bituminous coal fly ashes seem to be the most economically prospective in recovery of selected critical elements. The microanalysis has shown that iron cenospheres and plerospheres in fly ash contain, in addition to enamel and iron oxides (magnetite and hematite), iron spinels enriched in Co, Cr, Cu, Mn, Ni, W, and Zn.

Spatial distribution and potential biological risk of some metals in relation to granulometric content in core sediments from Chilika Lake, India.

PubMed

Barik, Saroja K; Muduli, Pradipta R; Mohanty, Bita; Rath, Prasanta; Samanta, Srikanta

2018-01-01

The article presents first systematic report on the concentration of selected major elements [iron (Fe) and manganese (Mn)] and minor elements [zinc (Zn), copper (Cu), chromium (Cr), lead (Pb), nickel (Ni), and cobalt (Co)] from the core sediment of Chilika Lake, India. The analyzed samples revealed higher content of Pb than the background levels in the entire study area. The extent of contamination from minor and major elements is expressed by assessing (i) the metal enrichments in the sediment through the calculations of anthropogenic factor (AF), pollution load index (PLI), Enrichment factor (EF), and geoaccumulation index (Igeo) and (ii) potential biological risks by the use of sediment quality guidelines like effect range median (ERM) and effect range low (ERL) benchmarks. The estimated indices indicated that sediment is enriched with Pb, Ni, Cr, Cu and Co. The enrichment of these elements seems to be due to the fine granulometric characteristics of the sediment with Fe and Mn oxyhydroxides being the main metal carriers and fishing boats using low grade paints, fuel, and fishing technology using lead beads fixed to fishing nets. Trace element input to the Chilika lake needs to be monitored with due emphasis on Cr and Pb contaminations since the ERM and ERL benchmarks indicated potential biological risk with these metals.

Hydrogen Isotope Geochemistry of Mariana Trough Lavas

NASA Astrophysics Data System (ADS)

Oleary, J.; Kitchen, N.; Eiler, J.

2002-12-01

Basaltic lavas from the Marianas trough vary in water content from values similar to mid-ocean ridge basalts (MORBs) to ten times those values. These variations plausibly reflect addition of subducted water to the mantle wedge, but must also reflect variations in extent of melting and crystallization-differentiation. We report hydrogen isotope data for 18 samples of lavas from the Mariana trough; these measurements, when combined with other geochemical data, constrain the relative proportions of subducted vs. 'primitive' water in their mantle sources. Previous measurements of the hydrogen isotope composition of Mariana trough lavas [1] found a correlation between dD and measured water content, consistent with two-component mixing between water in the ambient MORB source and water from the subducted slab, but include only four samples, only two of which have known major and minor element geochemistry. Our purpose is to confirm this result and expand it to include a more representative sampling. Our measurements made use of a recently developed technique for on-line stepped heating, water reduction and hydrogen isotope mass spectrometry [2]. This method is appropriate for relatively small samples of basaltic glass (ca. 100 μg to 1 mg) and up to 10 analyses can be performed per day. Its principle advantages for our purposes are that it can be applied to even small or glass-poor samples and it is fast enough to permit replication of all data and analysis of relatively large numbers of standards. Hydrogen isotope compositions of Mariana trough lavas vary between -74 per mil and -34 per mil (SMOW); this compares with a range of -46 to -32 per mil for related lavas in [1] and is similar to the previously observed range for back-arc-basin basalts generally (-70 to -32 per mil). Two-thirds of our sample suite span a small range in dD (-40+/-4 ). We suggest this average is the most representative value for back arc basin basalts measured to-date. Our data are inconsistent with the correlation between dD and measured water content suggested for back-arc basin basalts by [ref], even considering only lavas spanning a small range in MgO. This suggests one or both of two things: (1) melting and/or crystallization differentiation produce variations in water abundance unrelated to the abundance and dD of water in the mantle source; (2) there are three or more reservoirs in the mantle wedge of the Mariana arc, all of which differ in dD and water content (i.e., such that data do not define a simple line in a plot of dD vs. 1/H2O). The first of these is significant, but there is also evidence for the second. In particular, dD values decrease monotonically with increasing abundance of highly incompatible trace elements and with increasing La/Sm and K2O/H2O ratios; the lowest dD sample in our suite is an enriched basalt (La/Sm = 3.6) with an 'arc like' K2O content (0.71 wt. %). These data suggest that water in the mantle wedge of the Mariana arc is derived from three sources: ambient water common to the MORB source (ca. 0.02 wt. % H2O; dD ~ -65 to -75 per mil), subducted water (dD ~ -30 per mil) and an enriched source having high abundances of water and other incompatible trace elements and a dD value of ca. -80 per mil. [1] Poreda, 1985, EPSL 73, 244-254 [2] Eiler and Kitchen, 2001, GCA 65, 24, 4467-4479

Semantic Web Technology for Mapping and Applying Clinical Functional Assessment Information

DTIC Science & Technology

2014-03-01

the history and treatment of the injury or illness, is used by the MEB to determine whether the member has a medical condition that is incompatible...entities being measured are often represented by external terminologies , and assessments that are abstractions conceptually closer to the notions that...that describe the semantics of functional and related data elements, their relationships to standard terminologies and classifications, models of

Apollo 16 Evolved Lithology Sodic Ferrogabbro

NASA Technical Reports Server (NTRS)

Zeigler, Ryan; Jolliff, B. L.; Korotev, R. L.

2014-01-01

Evolved lunar igneous lithologies, often referred to as the alkali suite, are a minor but important component of the lunar crust. These evolved samples are incompatible-element rich samples, and are, not surprisingly, most common in the Apollo sites in (or near) the incompatible-element rich region of the Moon known as the Procellarum KREEP Terrane (PKT). The most commonly occurring lithologies are granites (A12, A14, A15, A17), monzogabbro (A14, A15), alkali anorthosites (A12, A14), and KREEP basalts (A15, A17). The Feldspathic Highlands Terrane is not entirely devoid of evolved lithologies, and rare clasts of alkali gabbronorite and sodic ferrogabbro (SFG) have been identified in Apollo 16 station 11 breccias 67915 and 67016. Curiously, nearly all pristine evolved lithologies have been found as small clasts or soil particles, exceptions being KREEP basalts 15382/6 and granitic sample 12013 (which is itself a breccia). Here we reexamine the petrography and geochemistry of two SFG-like particles found in a survey of Apollo 16 2-4 mm particles from the Cayley Plains 62283,7-15 and 62243,10-3 (hereafter 7-15 and 10-3 respectively). We will compare these to previously reported SFG samples, including recent analyses on the type specimen of SFG from lunar breccia 67915.

The dynamic relationship between polyandry and selfish genetic elements

PubMed Central

Wedell, Nina

2013-01-01

Selfish genetic elements (SGEs) are ubiquitous in eukaryotes and bacteria, and make up a large part of the genome. They frequently target sperm to increase their transmission success, but these manipulations are often associated with reduced male fertility. Low fertility of SGE-carrying males is suggested to promote polyandry as a female strategy to bias paternity against male carriers. Support for this hypothesis is found in several taxa, where SGE-carrying males have reduced sperm competitive ability. In contrast, when SGEs give rise to reproductive incompatibilities between SGE-carrying males and females, polyandry is not necessarily favoured, irrespective of the detrimental impact on male fertility. This is due to the frequency-dependent nature of these incompatibilities, because they will decrease in the population as the frequency of SGEs increases. However, reduced fertility of SGE-carrying males can prevent the successful population invasion of SGEs. In addition, SGEs can directly influence male and female mating behaviour, mating rates and reproductive traits (e.g. female reproductive tract length and male sperm). This reveals a potent and dynamic interaction between SGEs and polyandry highlighting the potential to generate sexual selection and conflict, but also indicates that polyandry can promote harmony within the genome by undermining the spread of SGEs. PMID:23339240

Trace elements and polycyclic aromatic hydrocarbons (PAHs) concentrations in deep Gulf of Mexico sediments

NASA Astrophysics Data System (ADS)

Wade, Terry L.; Soliman, Yousra; Sweet, Stephen T.; Wolff, Gary A.; Presley, Bobby J.

2008-12-01

The concentrations of polycyclic aromatic hydrocarbons (PAHs) and trace elements were determined for surface (top 2 cm) sediment samples collected during the deep Gulf of Mexico benthos (DGoMB) study .These elements and compounds are known to be toxic to organisms at high concentrations and may affect biological communities. There is no indication of major anthropogenic input of the elements Be, Co, Cr, Fe, Si, Tl, V, K, Mg, Ca, Sr and Zn, based on normalization to Al. The concentrations of these metals in the sediment are a function of the relative amounts of trace-metal-rich Mississippi River-derived silicate material and trace-metal-poor plankton-derived carbonate. This is not true for the elements Ba, Ni, Pb, Cd, As, Cu and Mn, whose concentrations show considerable scatter when normalized to Al and a general enrichment. On a normalized basis, Mn is enriched 5-10 fold, Cu and Ni 2-3 fold and Pb 2 fold over Mississippi River-derived material. These enrichments are likely the result of remobilization of metals from depths in the sediment column where reducing conditions exist. The Ba concentrations at selected sites are higher than those of average clay-rich sediments, but are typical of sediments from near oil well platforms in the northern Gulf of Mexico. In the case of Ba, it seems likely that the enrichments, as high as a factor of 10, are due to disposal of oil well drilling mud. The Ba-enriched samples are from the three shallowest water sites in the Mississippi Trough (sites MT1, 2 and 3) and from site C1 and WC5. All are in an area of intense petroleum exploration and development. PAH concentrations are also elevated at MT1, MT3 and C1. The total PAH concentration ranged from not detected (ND) to 1033 ng/g with a mean of 140 ng/g. Even at the sites most enriched in PAHs and trace elements, the concentrations are not at the levels expected to adversely affect the biota. However, these predicted non-effects are based on research using mostly near-shore estuarine species, not on the indigenous species at the sampling sites.

Determination of changes in the concentration and distribution of elements within olive drupes (cv. Leccino) from Se biofortified plants, using laser ablation inductively coupled plasma mass spectrometry.

PubMed

D'Amato, Roberto; Petrelli, Maurizio; Proietti, Primo; Onofri, Andrea; Regni, Luca; Perugini, Diego; Businelli, Daniela

2018-03-25

Biofortification of food crops has been used to increase the intake of Se in the human diet, even though this may change the concentration of other elements and modify the nutritional properties of the enriched food. Selenium biofortification programs should include routine assessment of the overall mineral composition of enriched plants. Laser ablation inductively coupled plasma mass spectrometry (LA ICP-MS) was used for the assessment of mineral composition of table olives. Olive trees were fertilized with sodium selenate before flowering. At harvest, the edible parts of drupes proved to be significantly enriched in Se, delivering 6.1 μg g -1 (39% of the RDA for five olives). Such enrichment was followed by significant changes in the concentrations of B, Mg, K, Cr, Mn, Fe and Cu in edible parts, which are discussed for their impact on food quality. The biofortification of olive plants has allowed the enrichment of fruits with selenium. Enrichment with selenium has caused an increase in the concentration of other elements, which can change the nutritional quality of the drupes. The analytical technique used well as a valuable tool for routinely determining the chemical composition of all fruit parts. © 2018 Society of Chemical Industry. © 2018 Society of Chemical Industry.

A Study on Urban Road Traffic Safety Based on Matter Element Analysis

PubMed Central

Hu, Qizhou; Zhou, Zhuping; Sun, Xu

2014-01-01

This paper examines a new evaluation of urban road traffic safety based on a matter element analysis, avoiding the difficulties found in other traffic safety evaluations. The issue of urban road traffic safety has been investigated through the matter element analysis theory. The chief aim of the present work is to investigate the features of urban road traffic safety. Emphasis was placed on the construction of a criterion function by which traffic safety achieved a hierarchical system of objectives to be evaluated. The matter element analysis theory was used to create the comprehensive appraisal model of urban road traffic safety. The technique was used to employ a newly developed and versatile matter element analysis algorithm. The matter element matrix solves the uncertainty and incompatibility of the evaluated factors used to assess urban road traffic safety. The application results showed the superiority of the evaluation model and a didactic example was included to illustrate the computational procedure. PMID:25587267

Quantitative statistical analysis of cis-regulatory sequences in ABA/VP1- and CBF/DREB1-regulated genes of Arabidopsis.

PubMed

Suzuki, Masaharu; Ketterling, Matthew G; McCarty, Donald R

2005-09-01

We have developed a simple quantitative computational approach for objective analysis of cis-regulatory sequences in promoters of coregulated genes. The program, designated MotifFinder, identifies oligo sequences that are overrepresented in promoters of coregulated genes. We used this approach to analyze promoter sequences of Viviparous1 (VP1)/abscisic acid (ABA)-regulated genes and cold-regulated genes, respectively, of Arabidopsis (Arabidopsis thaliana). We detected significantly enriched sequences in up-regulated genes but not in down-regulated genes. This result suggests that gene activation but not repression is mediated by specific and common sequence elements in promoters. The enriched motifs include several known cis-regulatory sequences as well as previously unidentified motifs. With respect to known cis-elements, we dissected the flanking nucleotides of the core sequences of Sph element, ABA response elements (ABREs), and the C repeat/dehydration-responsive element. This analysis identified the motif variants that may correlate with qualitative and quantitative differences in gene expression. While both VP1 and cold responses are mediated in part by ABA signaling via ABREs, these responses correlate with unique ABRE variants distinguished by nucleotides flanking the ACGT core. ABRE and Sph motifs are tightly associated uniquely in the coregulated set of genes showing a strict dependence on VP1 and ABA signaling. Finally, analysis of distribution of the enriched sequences revealed a striking concentration of enriched motifs in a proximal 200-base region of VP1/ABA and cold-regulated promoters. Overall, each class of coregulated genes possesses a discrete set of the enriched motifs with unique distributions in their promoters that may account for the specificity of gene regulation.

Finite Element Method Analysis of Nanoscratch Test for the Evaluation of Interface Adhesion Strength in Cu Thin Films on Si Substrate

NASA Astrophysics Data System (ADS)

Sekiguchi, Atsuko; Koike, Junichi

2008-01-01

Mechanical processes of the nanoscratch test are investigated using a finite element analysis of Cu/Ta/SiO2/Si multilayer films. The calculated stress distribution at the moment of delamination suggests that delamination occurs in a small region of approximately 100 nm. The driving force for delamination is the stress concentration due to strain-incompatibility at the Cu/Ta interface resulting from the large plastic deformation in Cu. The degree of stress concentration is found to depend on internal variables, such as plastic deformation, residual stress, and the elastic modulus, and on the magnitude of lateral force.

Macro and trace mineral constituents and radionuclides in mushrooms: health benefits and risks.

PubMed

Falandysz, Jerzy; Borovička, Jan

2013-01-01

This article reviews and updates data on macro and trace elements and radionuclides in edible wild-grown and cultivated mushrooms. A huge biodiversity of mushrooms and spread of certain species over different continents makes the study on their multi-element constituents highly challenging. A few edible mushrooms are widely cultivated and efforts are on to employ them (largely Agaricus spp., Pleurotus spp., and Lentinula edodes) in the production of selenium-enriched food (mushrooms) or nutraceuticals (by using mycelia) and less on species used by traditional medicine, e.g., Ganoderma lucidum. There are also attempts to enrich mushrooms with other elements than Se and a good example is enrichment with lithium. Since minerals of nutritional value are common constituents of mushrooms collected from natural habitats, the problem is however their co-occurrence with some hazardous elements including Cd, Pb, Hg, Ag, As, and radionuclides. Discussed is also the problem of erroneous data on mineral compounds determined in mushrooms.

Spatial distribution and historical trends of heavy metals in the sediments of petroleum producing regions of the Beibu Gulf, China.

PubMed

Yang, Jichao; Wang, Weiguo; Zhao, Mengwei; Chen, Bin; Dada, Olusegun A; Chu, Zhihui

2015-02-15

The concentrations of As, Sb, Hg, Pb, Cd, and Ba in the surface and core sediments of the oil and gas producing region of the Beibu Gulf were measured by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Atomic Fluorescence Spectrometry (AFS), and the spatial distribution and historical trends of these elements are discussed. The results show that the concentrations of these elements are highest near the platforms. The results of Enrichment Factor (EF) and Potential Ecological Risk Index (PERI) also reveal significantly higher enrichment around the platforms, which imply that the offshore petroleum production was the cause of the unusual distribution and severe enrichment of these elements in the study area. The environment around the platforms was highly laden with toxic elements, thereby representing a very high ecological risk to the environment of the study area. Copyright © 2014 Elsevier Ltd. All rights reserved.

Low-Metallicity Lead Stars: Comparison between Theory and Observations

NASA Astrophysics Data System (ADS)

Bisterzo, S.; Gallino, R.; Straniero, O.; Aoki, W.; Ryan, S.; Beers, T. C.

2006-07-01

We compare AGB theoretical models with spectroscopic abundances of a sample of very metal-poor, C-rich, s-rich and lead-rich stars observed at high-resolution spectroscopy. Fits are obtained for AGB models with different 13C-pocket efficiencies and initial masses. The two intrinsic indicators, [hs/ls] and [Pb/hs] versus [Fe/H], are analyzed. An extended analysis of all the observed elements is made, outlining apparent discrepancies for a few elements. The analysis of C and N abundances strengthen the need of a strong cool bottom process occurring during the AGB. A significant number of these stars are both s-enriched and r-enriched. For them, the envelope abundances are predicted by mass transfer from the more massive AGB companion in a binary system from a parental cloud already enriched in r-elements.

Generalization of mixed multiscale finite element methods with applications

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

Lee, C S

Many science and engineering problems exhibit scale disparity and high contrast. The small scale features cannot be omitted in the physical models because they can affect the macroscopic behavior of the problems. However, resolving all the scales in these problems can be prohibitively expensive. As a consequence, some types of model reduction techniques are required to design efficient solution algorithms. For practical purpose, we are interested in mixed finite element problems as they produce solutions with certain conservative properties. Existing multiscale methods for such problems include the mixed multiscale finite element methods. We show that for complicated problems, the mixedmore » multiscale finite element methods may not be able to produce reliable approximations. This motivates the need of enrichment for coarse spaces. Two enrichment approaches are proposed, one is based on generalized multiscale finte element metthods (GMsFEM), while the other is based on spectral element-based algebraic multigrid (rAMGe). The former one, which is called mixed GMsFEM, is developed for both Darcy’s flow and linear elasticity. Application of the algorithm in two-phase flow simulations are demonstrated. For linear elasticity, the algorithm is subtly modified due to the symmetry requirement of the stress tensor. The latter enrichment approach is based on rAMGe. The algorithm differs from GMsFEM in that both of the velocity and pressure spaces are coarsened. Due the multigrid nature of the algorithm, recursive application is available, which results in an efficient multilevel construction of the coarse spaces. Stability, convergence analysis, and exhaustive numerical experiments are carried out to validate the proposed enrichment approaches. iii« less

On volatile element trends in gas-rich meteorites

NASA Technical Reports Server (NTRS)

Bart, G.; Lipschutz, M. E.

1979-01-01

Ten volatile elements (and non-volatile Co) in co-existing light and dark portions of 5 gas-rich chondrites were studied. Patterns of distinct but non-uniform enrichment by dark admixing material are revealed. The dark admixing material is enriched in Cs; Bi and Tl covary in it. It is compositionally unique from known types of primitive materials and is apparently not derived by secondary processes from such materials.

The trace element chemistry of CaS in enstatite chondrites and some implications regarding its origin

NASA Technical Reports Server (NTRS)

Larimer, John W.; Ganapathy, R.

1987-01-01

The trace element distribution in oldhamite (CaS) extracted from enstatite chondrites was determined by INAA. Prior to extraction, the petrologic setting of the grains was studied microscopically, and their minor element contents determined by microprobe analysis; samples that displayed a wide range of minor element contents were selected for detailed elementary analysis. Those samples of CaS suspected to be more primitive on the basis of their minor element and petrologic siting contain the entire inventory of the host meteorite's light REE (LREE) and Eu, plus 30-50 percent of the heavy-REE inventory. In less primitive samples, the LREE are less enriched although Eu remains highly concentrated. Several other elements, including lithophiles and chalcophiles, are most enriched in the most primitive CaS. It is suggested that oldhamite played a key role in the redistribution of these elements during the metamorphism and evolution of enstatite-rich material.

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).

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

Drug incompatibilities in the adult intensive care unit of a university hospital

PubMed Central

Marsilio, Naiane Roveda; da Silva, Daiandy; Bueno, Denise

2016-01-01

Objectives This study sought to identify the physical and chemical incompatibilities among the drugs administered intravenously to patients admitted to an adult intensive care unit. We also aimed to establish pharmaceutical guidelines for administering incompatible drugs. Methods This cross-sectional, prospective, and quantitative study was conducted from July to September 2015. Drug incompatibilities were identified based on an analysis of the patient prescriptions available in the hospital online management system. A pharmaceutical intervention was performed using the guidelines on the preparation and administration of incompatible drugs. Adherence to those guidelines was subsequently assessed among the nursing staff. Results A total of 100 prescriptions were analyzed; 68 were incompatible with the intravenous drugs prescribed. A total of 271 drug incompatibilities were found, averaging 4.0 ± 3.3 incompatibilities per prescription. The most commonly found drug incompatibilities were between midazolam and hydrocortisone (8.9%), between cefepime and midazolam (5.2%), and between hydrocortisone and vancomycin (5.2%). The drugs most commonly involved in incompatibilities were midazolam, hydrocortisone, and vancomycin. The most common incompatibilities occurred when a drug was administered via continuous infusion and another was administered intermittently (50%). Of the 68 prescriptions that led to pharmaceutical guidelines, 45 (66.2%) were fully adhered to by the nursing staff. Conclusion Patients under intensive care were subjected to a high rate of incompatibilities. Drug incompatibilities can be identified and eliminated by the pharmacist on the multidisciplinary team, thereby reducing undesirable effects among patients. PMID:27410410

Elements and inorganic ions as source tracers in recent Greenland snow

NASA Astrophysics Data System (ADS)

Lai, Alexandra M.; Shafer, Martin M.; Dibb, Jack E.; Polashenski, Chris M.; Schauer, James J.

2017-09-01

Atmospheric transport of aerosols leads to deposition of impurities in snow, even in areas of the Arctic as remote as Greenland. Major ions (e.g. Na+, Ca2+, NH4+, K+, SO42-) are frequently used as tracers for common aerosol sources (e.g. sea spray, dust, biomass burning, anthropogenic emissions). Trace element data can supplement tracer ion data by providing additional information about sources. Although many studies have considered either trace elements or major ions, few have reported both. This study determined total and water-soluble concentrations of 31 elements (Al, As, Ca, Cd, Ce, Co, Cr, Dy, Eu, Fe, Gd, K, La, Mg, Mn, Na, Nb, Nd, Pb, Pr, S, Sb, Si, Sm, Sn, Sr, Ti, V, U, Y, Zn) in shallow snow pits at 22 sampling sites in Greenland, along a transect from Summit Station to sites in the northwest. Black carbon (BC) and inorganic ions were measured in colocated samples. Sodium, which is typically used as a tracer of sea spray, did not appear to have any non-marine sources. The rare earth elements, alkaline earth elements (Mg, Ca, Sr), and other crustal elements (Fe, Si, Ti, V) were not enriched above crustal abundances relative to Al, indicating that these elements are primarily dust sourced. Calculated ratios of non-sea salt Ca (nssCa) to estimated dust mass affirm the use of nssCa as a dust tracer, but suggest up to 50% uncertainty in that estimate in the absence of other crustal element data. Crustal enrichment factors indicated that As, Cd, Pb, non-sea-salt S, Sb, Sn, and Zn were enriched in these samples, likely by anthropogenic sources. Principal component analysis indicated more than one crustal factor, and a variety of factors related to anthropogenically enriched elements. Analysis of trace elements alongside major tracer ions does not change interpretation of ion-based source attribution for sources that are well-characterized by ions, but is valuable for assessing uncertainty in source attribution and identifying sources not represented by major ions.

#eVALUate: Monetizing Service Acquisition Trade-offs Using the QUALITY-INFUSED Price Methodology

DTIC Science & Technology

2016-04-01

methodologies that are incompatible with the characteristics of services. These methodologies involve best-value source selection and contractor ...defense contractors for services, it lacks the key elements at the strategic and tactical levels to make service contracts a managed outcome (U.S...Regulation (FAR) defines a service contract as a “contract that directly engages the time and effort of a contractor whose primary purpose is to

Effect of mining and related activities on the sediment trace element geochemistry of Lake Coeur D'Alene, Idaho, USA. Part I: Surface sediments

USGS Publications Warehouse

Horowitz, Arthur J.; Elrick, Kent A.; Cook, Robert B.

1993-01-01

During the summer of 1989 surface sediment samples were collected in Lake Coeur d'Alene, the Coeur d'Alene River and the St Joe River, Idaho, at a density of approximately one sample per square kilometre. Additional samples were collected from the banks of the South Fork of the Coeur d'Alene and the Coeur d'Alene Rivers in 1991. All the samples were collected to determine trace element concentrations, partitioning and distribution patterns, and to relate them to mining, mining related and discharge operations that have occurred in the Coeur d'Alene district since the 1880s, some of which are ongoing.Most of the surface sediments in Lake Coeur d'Alene north of Conkling Point and Carey Bay are substantially enriched in Ag, As, Cu, Cd, Hg, Pb, Sb and Zn relative to unaffected sediments in the southern portion of the lake near the St Joe River. All the trace element enriched sediments are extremely fine grained (mean grain sizes « 63 μm). Most of the enriched trace elements, based on both the chemical analyses of separated heavy and light mineral fractions and a two step sequential extraction procedure, are associated with an operationally defined Fe oxide phase; much smaller percentages are associated either with operationally defined organics/sulphides or refractory phases.The presence, concentration and distribution of the Fe oxides and heavy minerals indicates that a substantial portion of the enriched trace elements are probably coming from the Coeur d'Alene River, which is serving as a point source. Within the lake, this relatively simple point source pattern is complicated by a combination of (1) the formation of trace element rich authigenic Fe oxides that appear to have reprecipitated from material solubilized from anoxic bed sediments and (2) physical remobilization by currents and wind driven waves. The processes that have caused the trace element enrichment in the surface sediments of Lake Coeur d'Alene are likely to continue for the foreseeable future.

Trace elements in streambed sediments of small subtropical streams on O'ahu, Hawai'i: Results from the USGS NAWQA program

USGS Publications Warehouse

De Carlo, E. H.; Tomlinson, M.S.; Anthony, S.S.

2005-01-01

Data are presented for trace element concentrations determined in the <63 ??m fraction of streambed sediment samples collected at 24 sites on the island of O'ahu, Hawai'i. Sampling sites were classified as urban, agricultural, mixed (urban/agricultural), or forested based on their dominant land use, although the mixed land use at selected sampling sites consisted of either urban and agricultural or forested and agricultural land uses. Forest dominated sites were used as reference sites for calculating enrichment factors. Trace element concentrations were compared to concentrations from studies conducted in the conterminous United States using identical methods and to aquatic-life guidelines provided by the Canadian Council of Ministers of the Environment. A variety of elements including Pb, Cr, Cu and Zn exceeded the aquatic-life guidelines in selected samples. All of the Cr and Zn values and 16 of 24 Cu values exceeded their respective guidelines. The potential toxicity of elements exceeding guidelines, however, should be considered in the context of strong enrichments of selected trace elements attributable to source rocks in Hawai'i, as well as in the context of the abundance of fine-grained sediment in the streambed of O'ahu streams. Statistical methods including cluster analysis, Kruskal-Wallis non-parametric test, correlation analysis, and principal component analysis (PCA) were used to evaluate differences and elucidate relationships between trace elements and sites. Overall, trace element distributions and abundances can be correlated to three principal sources of elements. These include basaltic rocks of the volcanic edifice (Fe, Al, Ni, Co, Cr, V and Cu), carbonate/seawater derived elements (Mg, Ca, Na and Sr), and elements enriched owing to anthropogenic activity (P, Sn, Cd, Sn, Ba and Pb). Anthropogenic enrichment gradients were observed for Ba, Cd, Pb, Sn and Zn in the four streams in which sediments were collected upstream and downstream. The findings of this study are generally similar to but differ slightly from previous work on sediments and suspended particulate matter in streams, from two urban watersheds of O'ahu, Hawai'i. Inter-element associations in the latter were often stronger and indicated a mixture of anthropogenic, agricultural and basaltic sources of trace elements. Some elements fell into different statistical categories in the two studies, owing in part to differences in study design and the hydrogeological constraints on the respective study areas.

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

NASA Astrophysics Data System (ADS)

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

2016-04-01

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

Trace-element evidence for the origin of desert varnish by direct aqueous atmospheric deposition

NASA Astrophysics Data System (ADS)

Thiagarajan, Nivedita; Aeolus Lee, Cin-Ty

2004-07-01

Smooth rock surfaces in arid environments are often covered with a thin coating of Fe-Mn oxyhydroxides known as desert varnish. It is debated whether such varnish is formed (a) by slow diagenesis of dust particles deposited on rock surfaces, (b) by leaching from the underlying rock substrate, or (c) by direct deposition of dissolved constituents in the atmosphere. Varnishes collected from smooth rock surfaces in the Mojave Desert and Death Valley, California are shown here to have highly enriched and fractionated trace-element abundances relative to upper continental crust (UCC). They are highly enriched in Co, Ni, Pb and the rare-earth elements (REEs). In particular, they have anomalously high Ce/La and low Y/Ho ratios. These features can only be explained by preferential scavenging of Co, Ni, Pb and the REEs by Fe-Mn oxyhydroxides in an aqueous environment. High field strength elements (HFSEs: Zr, Hf, Ta, Nb, Th), however, show only small enrichments despite the fact that these elements should also be strongly scavenged by Fe-Mn oxyhydroxides. This suggests that their lack of enrichment is a feature inherited from a solution initially poor in HFSEs. The first two scenarios for varnish formation can be ruled out as follows. The high enrichment factors of Fe, Mn and many trace elements cannot be generated by mass loss associated with post-depositional diagenesis of dust particles because such a process predicts only a small increase in concentration. In addition, the highly fractionated abundance patterns of particle reactive element pairs (e.g., Ce/La and Y/Ho) rules out leaching of the rock substrate. This is because if leaching were to occur, varnishes would grow from the inside to the outside, and thus any particle-reactive trace element leached from the substrate would be quantitatively sequestered in the Fe-Mn oxyhydroxide layers, prohibiting any significant elemental fractionations. One remaining possibility is that the Fe, Mn and trace metals in varnish are derived from leaching of dust particles entrained in rain or fog droplets either in the atmosphere or during wet atmospheric deposition. The high trace metal enrichment factors require that most of the dust was physically removed before or during varnish formation. The remaining aqueous counterpart would be depleted in HFSEs and Th relative to the REEs, Co, Ni and Pb because the former are more insoluble and hence largely retained in the removed dust fraction. The high Ce/La ratios suggest that precipitation of trace metals may have been governed by equilibrium partitioning in an excess of wet atmospheric deposition. If varnishes are indeed derived from wet atmospheric deposition, they may provide a record of the aqueous component of atmospheric dust inputs to various environments.

Petrological significance of high-pressure ultramafic xenoliths from ultrapotassic rocks of Central Italy

NASA Astrophysics Data System (ADS)

Conticelli, Sandro; Peccerillo, Angelo

1989-08-01

Two suites of ultramafic xenoliths have been found in ultrapotassic lavas from the 0.9 Ma old Torre Alfina volcano sited at the northern border of the Vulsinian district (Central Italy). One group of Xenoliths consists of spinel-bearing lherzolites, harzburgites, minor wherlites and dunites with a maximum size of 3-4 cm. Some samples contain discrete laths of phlogopite. A second class consists of phlogopite-rich, glass-bearing peridotites. The first suite displays textural characteristics such as triple points, deformed olivine with well developed kink banding and porphyroclastic textures indicating equilibration at high pressure. Pressure estimates give values in the range 1.3-2.5 GPa, corresponding to mantle depths in the area, where the present-day Moho is about 25 km deep. Equilibration temperatures have been estimated in the range between 950-1000°C. The chemical composition of some phases, such as the very high Fo contents of olivines (up to Fo 94 in harzburgites), Mg content of orthopyroxenes and {Cr}/{Cr}+Al ratios of clinopyroxenes and spinels, suggest that these xenoliths represent peridotites which suffered different degrees of partial melting before being incorporated into the Torre Alfina magma. On the other hand, the occurrence of phlogopite speaks for metasomatic events. The phlogopite-rich, glass-bearing xenoliths consist of phlogopite, olivine, clinopyroxene, rare orthopyroxene and glass. Apatite is the most common accessory. Olivine is present in both euhedral and strained crystals. A few relics of protogranular textures are also observed. Textural and chemical evidence suggests that these xenoliths represent mica-rich peridotites which have undergone phlogopite breakdown during rapid rise to the surface with the development of a K-rich liquid which reacted with mafic phases producing a rapid growth of olivine and, to a lower extent, pyroxene. Originally, these xenoliths may have represented intensively metasomatized upper mantle. However, a cumulitic origin from previous potassic magmatic events cannot be excluded. The host lavas have compositions intermediate between high-silica lamproite and Roman-type ultrapotassic rock. They have high abundances of incompatible elements and radiogenic Sr, coupled with high Mg content, {MgO}/{CaO}, Ni and Cr. These features support a genesis in a residual upper mantle which has suffered partial melting with the extraction of basaltic liquids, followed by metasomatic events which caused an enrichment in incompatible elements and radiogenic Sr. The presence of mantle-derived ultramafic xenoliths in the torre Alfina lavas testifies for a rapid uprise of the magma which reached the surface without suffering fractional crystallization and significant interaction with the upper crust. Accordingly, the Torre Alfina lavas represent an unique example of primitive potassic liquid in Central Italy.

Petrological significance of high-pressure ultramafic xenoliths from ultrapotassic rocks of Central Italy

NASA Astrophysics Data System (ADS)

Conticelli, Sandro; Peccerillo, Angelo

1990-08-01

Two suites of ultramafic xenoliths have been found in ultrapotassic lavas from the 0.9 Ma old Torre Alfina volcano sited at the northern border of the Vulsinian district (Central Italy). One group of Xenoliths consists of spinel-bearing lherzolites, harzburgites, minor wherlites and dunites with a maximum size of 3-4 cm. Some samples contain discrete laths of phlogopite. A second class consists of phlogopite-rich, glass-bearing peridotites. The first suite displays textural characteristics such as triple points, deformed olivine with well developed kink banding and porphyroclastic textures indicating equilibration at high pressure. Pressure estimates give values in the range 1.3-2.5 GPa, corresponding to mantle depths in the area, where the present-day Moho is about 25 km deep. Equilibration temperatures have been estimated in the range between 950-1000°C. The chemical composition of some phases, such as the very high Fo contents of olivines (up to Fo94 in harzburgites), Mg content of orthopyroxenes and {Cr}/{Cr}+Al ratios of clinopyroxenes and spinels, suggest that these xenoliths represent peridotites which suffered different degrees of partial melting before being incorporated into the Torre Alfina magma. On the other hand, the occurrence of phlogopite speaks for metasomatic events. The phlogopite-rich, glass-bearing xenoliths consist of phlogopite, olivine, clinopyroxene, rare orthopyroxene and glass. Apatite is the most common accessory. Olivine is present in both euhedral and strained crystals. A few relics of protogranular textures are also observed. Textural and chemical evidence suggests that these xenoliths represent mica-rich peridotites which have undergone phlogopite breakdown during rapid rise to the surface with the development of a K-rich liquid which reacted with mafic phases producing a rapid growth of olivine and, to a lower extent, pyroxene. Originally, these xenoliths may have represented intensively metasomatized upper mantle. However, a cumulitic origin from previous potassic magmatic events cannot be excluded. The host lavas have compositions intermediate between high-silica lamproite and Roman-type ultrapotassic rock. They have high abundances of incompatible elements and radiogenic Sr, coupled with high Mg content, {MgO}/{CaO}, Ni and Cr. These features support a genesis in a residual upper mantle which has suffered partial melting with the extraction of basaltic liquids, followed by metasomatic events which caused an enrichment in incompatible elements and radiogenic Sr. The presence of mantle-derived ultramafic xenoliths in the torre Alfina lavas testifies for a rapid uprise of the magma which reached the surface without suffering fractional crystallization and significant interaction with the upper crust. Accordingly, the Torre Alfina lavas represent an unique example of primitive potassic liquid in Central Italy.

Effective delayed neutron fraction and prompt neutron lifetime of Tehran research reactor mixed-core.

PubMed

Lashkari, A; Khalafi, H; Kazeminejad, H

2013-05-01

In this work, kinetic parameters of Tehran research reactor (TRR) mixed cores have been calculated. The mixed core configurations are made by replacement of the low enriched uranium control fuel elements with highly enriched uranium control fuel elements in the reference core. The MTR_PC package, a nuclear reactor analysis tool, is used to perform the analysis. Simulations were carried out to compute effective delayed neutron fraction and prompt neutron lifetime. Calculation of kinetic parameters is necessary for reactivity and power excursion transient analysis. The results of this research show that effective delayed neutron fraction decreases and prompt neutron lifetime increases with the fuels burn-up. Also, by increasing the number of highly enriched uranium control fuel elements in the reference core, the prompt neutron lifetime increases, but effective delayed neutron fraction does not show any considerable change.

Effective delayed neutron fraction and prompt neutron lifetime of Tehran research reactor mixed-core

PubMed Central

Lashkari, A.; Khalafi, H.; Kazeminejad, H.

2013-01-01

In this work, kinetic parameters of Tehran research reactor (TRR) mixed cores have been calculated. The mixed core configurations are made by replacement of the low enriched uranium control fuel elements with highly enriched uranium control fuel elements in the reference core. The MTR_PC package, a nuclear reactor analysis tool, is used to perform the analysis. Simulations were carried out to compute effective delayed neutron fraction and prompt neutron lifetime. Calculation of kinetic parameters is necessary for reactivity and power excursion transient analysis. The results of this research show that effective delayed neutron fraction decreases and prompt neutron lifetime increases with the fuels burn-up. Also, by increasing the number of highly enriched uranium control fuel elements in the reference core, the prompt neutron lifetime increases, but effective delayed neutron fraction does not show any considerable change. PMID:24976672

Experimental determination of crystal/melt partitioning of Ga and Ge in the system forsterite-anorthite-diopside

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

Malvin, D.J.; Drake, M.J.

1987-08-01

The crystal/liquid partitioning of Ga and Ge has been measured experimentally between forsterite, diopside, anorthite and spinel and melts in the pseudoternary system forsterite-anorthite-diopside at one atmosphere pressure and 1300/sup 0/C. Gallium is incompatible with forsterite and diopside, is only slightly incompatible in anorthite, and is highly compatible in spinel. The partition coefficient for Ge is within a factor of two of unity for forsterite, diopside, and anorthite, but Ge is incompatible in spinel (D (Ge) = 0.1). The coefficients for the exchange of Ga and Al and the exchange of Ge and Si between minerals and melts generally aremore » within a factor of two of unity, as it expected from the geochemical coherence of these element pairs in natural samples. The application of these results to the interpretation of natural basaltic and mantle samples from the Earth and basalts from the Moon and the Shergottite Parent Body demonstrates that it is possible to discriminate between different mantle source compositions using Ga/Al and Ge/Si ratios. The Ge variation among lunar mare basalts may be indicative of a heterogeneous lunar mantle. The substantial depletion of Ge in Chassigny relative to the other SNC meteorites may be evidence of either a heterogeneous Shergottite Parent Body (SPB) mantle, or of different geochemical behavior for Ge in the SPB.« less

Trace element partitioning behavior of coal gangue-fired CFB plant: experimental and equilibrium calculation.

PubMed

Zhang, Yingyi; Nakano, Jinichiro; Liu, Lili; Wang, Xidong; Zhang, Zuotai

2015-10-01

Energy recovery is a promising method for coal gangue utilization, during which the prevention of secondary pollution, especially toxic metal emission, is a significant issue in the development of coal gangue utilization. In the present study, investigation into trace element partitioning behavior from a coal gangue-fired power plant in Shanxi province, China, has been conducted. Besides the experimental analysis, thermodynamic equilibrium calculation was also conducted to help the further understanding on the effect of different parameters. Results showed that Hg, As, Be, and Cd were highly volatile elements in the combustion of coal gangue, which were notably enriched in fly ash and may be emitted into the environment via the gas phase. Cr and Mn were mostly non-volatile and were enriched in the bottom ash. Pb, Co, Zn, Cu, and Ni were semi-volatile elements and were enriched in the fly ash to varying degrees. Equilibrium calculations show that the air/fuel ratio and the presence of Cl highly affect the element volatility. The presence of mineral phases, such as aluminosilicates, depresses the volatility of elements by chemical immobilization and competition in Cl. The coal gangue, fly ash, and bottom ash all passed the toxicity characteristic leaching procedure (TCLP), and their alkalinity buffers the acidity of the solution and contributes to the low solubility of the trace elements.

NEUTRON-CAPTURE ELEMENT ABUNDANCES IN MAGELLANIC CLOUD PLANETARY NEBULAE

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

Mashburn, A. L.; Sterling, N. C.; Madonna, S.

We present near-infrared spectra of 10 planetary nebulae (PNe) in the Large and Small Magellanic Clouds (LMC and SMC), acquired with the FIRE and GNIRS spectrometers on the 6.5 m Baade and 8.1 m Gemini South Telescopes, respectively. We detect Se and/or Kr emission lines in eight of these objects, the first detections of n -capture elements in Magellanic Cloud PNe. Our abundance analysis shows large s -process enrichments of Kr (0.6–1.3 dex) in the six PNe in which it was detected, and Se is enriched by 0.5–0.9 dex in five objects. We also estimate upper limits to Rb andmore » Cd abundances in these objects. Our abundance results for the LMC are consistent with the hypothesis that PNe with 2–3 M {sub ⊙} progenitors dominate the bright end of the PN luminosity function in young gas-rich galaxies. We find no significant correlations between s -process enrichments and other elemental abundances, central star temperature, or progenitor mass, though this is likely due to our small sample size. We determine S abundances from our spectra and find that [S/H] agrees with [Ar/H] to within 0.2 dex for most objects, but is lower than [O/H] by 0.2–0.4 dex in some PNe, possibly due to O enrichment via third dredge-up. Our results demonstrate that n -capture elements can be detected in PNe belonging to nearby galaxies with ground-based telescopes, allowing s -process enrichments to be studied in PN populations with well-determined distances.« less

Possible lunar ores

NASA Technical Reports Server (NTRS)

Gillett, Stephen L.

1991-01-01

Despite the conventional wisdom that there are no lunar ores, geochemical considerations suggest that local concentrations of useful rare elements exist on the Moon in spite of its extreme dryness. The Moon underwent protracted igneous activity in its history, and certain magmatic processes can concentrate incompatible elements even if anhydrous. Such processes include: (1) separation of a magma into immiscible liquid phases (depending on composition, these could be silicate-silicate, silicate-oxide, silicate-sulfide, or silicate-salt); (2) cumulate deposits in layered igneous intrusions; and (3) concentrations of rare, refractory, lithophile elements (e.g., Be, Li, Zr) in highly differentiated, silica-rich magmas, as in the lunar granites. Terrestrial mining experience indicates that the single most important characteristic of a potential ore is its concentration of the desire element. The utility of a planet as a resource base is that the welter of interacting processes over geologic time can concentrate rare element automatically. This advantage is squandered if adequate exploration for ores is not first carried out.

Geochemical stratigraphy of two regolith cores from the Central Highlands of the moon

NASA Technical Reports Server (NTRS)

Korotev, R. L.

1991-01-01

High-resolution concentration profiles are presented for 20-22 chemical elements in the under 1-mm grain-size fractions of 60001-7 and 60009/10. Emphasis is placed on the stratigraphic features of the cores, and the fresh results are compared with those of previous petrographic and geochemical studies. For elements associated with major mineral phases, the variations in concentration in both cores exceed that observed in some 40 samples of surface and trench soils. Most of the variation in lithophile element concentrations at depths of 18 to 21 cm results from the mixing of two components - oil that is relatively mafic and rich in incompatible trace elements (ITEs), and coarse-grained anorthosite. The linearity of mixing lines on two-element concentration plots argues that the relative abundances of these various subcomponents are sufficiently uniform from sample to sample and from region to region in the core that the mixture behaves effectively as a single component. Soils at depths of 52-55 cm exhibit very low concentrations of ITEs.

Abundance patterns of the light neutron-capture elements in very and extremely metal-poor stars

NASA Astrophysics Data System (ADS)

Spite, F.; Spite, M.; Barbuy, B.; Bonifacio, P.; Caffau, E.; François, P.

2018-03-01

Aims: The abundance patterns of the neutron-capture elements in metal-poor stars provide a unique record of the nucleosynthesis products of the earlier massive primitive objects. Methods: We measured new abundances of so-called light neutron-capture of first peak elements using local thermodynamic equilibrium (LTE) 1D analysis; this analysis resulted in a sample of 11 very metal-poor stars, from [Fe/H] = -2.5 to [Fe/H] = -3.4, and one carbon-rich star, CS 22949-037 with [Fe/H] = -4.0. The abundances were compared to those observed in two classical metal-poor stars: the typical r-rich star CS 31082-001 ([Eu/Fe] > +1.0) and the r-poor star HD 122563 ([Eu/Fe] < 0.0), which are known to present a strong enrichment of the first peak neutron-capture elements relative to the second peak. Results: Within the first peak, the abundances are well correlated in analogy to the well-known correlation inside the abundances of the second-peak elements. In contrast, there is no correlation between any first peak element with any second peak element. We show that the scatter of the ratio of the first peak abundance over second peak abundance increases when the mean abundance of the second peak elements decreases from r-rich to r-poor stars. We found two new r-poor stars that are very similar to HD 122563. A third r-poor star, CS 22897-008, is even more extreme; this star shows the most extreme example of first peak elements enrichment to date. On the contrary, another r-poor star (BD-18 5550) has a pattern of first peak elements that is similar to the typical r-rich stars CS 31082-001, however this star has some Mo enrichment. Conclusions: The distribution of the neutron-capture elements in our very metal-poor stars can be understood as the combination of at least two mechanisms: one that enriches the forming stars cloud homogeneously through the main r-process and leads to an element pattern similar to the r-rich stars, such as CS 31082-001; and another that forms mainly lighter, first peak elements. Based on observations collected at the European Organisation for Astronomical Research in the Southern Hemisphere under ESO programme 165.N-0276(A), (PI R.Cayrel).

Pyrosequencing®-Based Identification of Low-Frequency Mutations Enriched Through Enhanced-ice-COLD-PCR.

PubMed

How-Kit, Alexandre; Tost, Jörg

2015-01-01

A number of molecular diagnostic assays have been developed in the last years for mutation detection. Although these methods have become increasingly sensitive, most of them are incompatible with a sequencing-based readout and require prior knowledge of the mutation present in the sample. Consequently, coamplification at low denaturation (COLD)-PCR-based methods have been developed and combine a high analytical sensitivity due to mutation enrichment in the sample with the identification of known or unknown mutations by downstream sequencing experiments. Among these methods, the recently developed Enhanced-ice-COLD-PCR appeared as the most powerful method as it outperformed the other COLD-PCR-based methods in terms of the mutation enrichment and due to the simplicity of the experimental setup of the assay. Indeed, E-ice-COLD-PCR is very versatile as it can be used on all types of PCR platforms and is applicable to different types of samples including fresh frozen, FFPE, and plasma samples. The technique relies on the incorporation of an LNA containing blocker probe in the PCR reaction followed by selective heteroduplex denaturation enabling amplification of the mutant allele while amplification of the wild-type allele is prevented. Combined with Pyrosequencing(®), which is a very quantitative high-resolution sequencing technology, E-ice-COLD-PCR can detect and identify mutations with a limit of detection down to 0.01 %.

Pliocene granodioritic knoll with continental crust affinities discovered in the intra-oceanic Izu-Bonin-Mariana Arc: Syntectonic granitic crust formation during back-arc rifting

NASA Astrophysics Data System (ADS)

Tani, Kenichiro; Dunkley, Daniel J.; Chang, Qing; Nichols, Alexander R. L.; Shukuno, Hiroshi; Hirahara, Yuka; Ishizuka, Osamu; Arima, Makoto; Tatsumi, Yoshiyuki

2015-08-01

A widely held hypothesis is that modern continental crust of an intermediate (i.e. andesitic) bulk composition forms at intra-oceanic arcs through subduction zone magmatism. However, there is a critical paradox in this hypothesis: to date, the dominant granitic rocks discovered in these arcs are tonalite, rocks that are significantly depleted in incompatible (i.e. magma-preferred) elements and do not geochemically and petrographically represent those of the continents. Here we describe the discovery of a submarine knoll, the Daisan-West Sumisu Knoll, situated in the rear-arc region of the intra-oceanic Izu-Bonin-Mariana Arc. Remotely-operated vehicle surveys reveal that this knoll is made up entirely of a 2.6 million year old porphyritic to equigranular granodiorite intrusion with a geochemical signature typical of continental crust. We present a model of granodiorite magma formation that involves partial remelting of enriched mafic rear-arc crust during the initial phase of back-arc rifting, which is supported by the preservation of relic cores inherited from initial rear-arc source rocks within magmatic zircon crystals. The strong extensional tectonic regime at the time of intrusion may have allowed the granodioritic magma to be emplaced at an extremely shallow level, with later erosion of sediment and volcanic covers exposing the internal plutonic body. These findings suggest that rear-arc regions could be the potential sites of continental crust formation in intra-oceanic convergent margins.

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

NASA Astrophysics Data System (ADS)

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

2004-01-01

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

Long-term risk in a recently active volcanic system: Evaluation of doses and indoor radiological risk in the quaternary Vulsini Volcanic District (Central Italy)

NASA Astrophysics Data System (ADS)

Capaccioni, B.; Cinelli, G.; Mostacci, D.; Tositti, L.

2012-12-01

Volcanic rocks in the Vulsini Volcanic District (Central Italy) contain high concentrations of 238U, 232Th and 40K due to subduction-related metasomatic enrichment of incompatible elements in the mantle source coupled with magma differentiation within the upper crust. Due to their favorable mechanical properties they have been extensively used for construction since the Etruscan age. In the old buildings of the Bolsena village, one of the most populated ancient village in the area, the major source of indoor radioactivity is 222Rn, a radioactive noble gas descendant of 238U. Direct 222Rn indoor measurements have detected extremely high values in the old center due to the combined effect of building materials, radon fluxes from the volcanic basement and low air exchange rates. In these cases the evaluated risk of developing lung cancer within a 75 year lifetime reaches up to 40% for ever smokers. Simulations of "standard rooms" built with different tuffs and lavas collected from the Vulsini Volcanic District have also provided estimations of the effective doses and lifetime risk for radiogenic cancer. Other than by the method adopted for calculation, the total evaluated risk for each volcanic rock depends on different parameters, such as: radionuclide content, radon emanation power, occupancy factor and air exchange rate. Occupancy factor and air exchange rate appear as the only controlling parameters able to mitigate the indoor radiological risk.

Uranium mineralization in fluorine-enriched volcanic rocks

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

Burt, D.M.; Sheridan, M.F.; Bikun, J.

1980-09-01

Several uranium and other lithophile element deposits are located within or adjacent to small middle to late Cenozoic, fluorine-rich rhyolitic dome complexes. Examples studied include Spor Mountain, Utah (Be-U-F), the Honeycomb Hills, Utah (Be-U), the Wah Wah Mountains, Utah (U-F), and the Black Range-Sierra Cuchillo, New Mexico (Sn-Be-W-F). The formation of these and similar deposits begins with the emplacement of a rhyolitic magma, enriched in lithophile metals and complexing fluorine, that rises to a shallow crustal level, where its roof zone may become further enriched in volatiles and the ore elements. During initial explosive volcanic activity, aprons of lithicrich tuffsmore » are erupted around the vents. These early pyroclastic deposits commonly host the mineralization, due to their initial enrichment in the lithophile elements, their permeability, and the reactivity of their foreign lithic inclusions (particularly carbonate rocks). The pyroclastics are capped and preserved by thick topaz rhyolite domes and flows that can serve as a source of heat and of additional quantities of ore elements. Devitrification, vapor-phase crystallization, or fumarolic alteration may free the ore elements from the glassy matrix and place them in a form readily leached by percolating meteoric waters. Heat from the rhyolitic sheets drives such waters through the system, generally into and up the vents and out through the early tuffs. Secondary alteration zones (K-feldspar, sericite, silica, clays, fluorite, carbonate, and zeolites) and economic mineral concentrations may form in response to this low temperature (less than 200 C) circulation. After cooling, meteoric water continues to migrate through the system, modifying the distribution and concentration of the ore elements (especially uranium).« less

Geospatial analysis of residential proximity to open-pit coal mining areas in relation to micronuclei frequency, particulate matter concentration, and elemental enrichment factors.

PubMed

Espitia-Pérez, Lyda; Arteaga-Pertuz, Marcia; Soto, José Salvador; Espitia-Pérez, Pedro; Salcedo-Arteaga, Shirley; Pastor-Sierra, Karina; Galeano-Páez, Claudia; Brango, Hugo; da Silva, Juliana; Henriques, João A P

2018-09-01

During coal surface mining, several activities such as drilling, blasting, loading, and transport produce large quantities of particulate matter (PM) that is directly emitted into the atmosphere. Occupational exposure to this PM has been associated with an increase of DNA damage, but there is a scarcity of data examining the impact of these industrial operations in cytogenetic endpoints frequency and cancer risk of potentially exposed surrounding populations. In this study, we used a Geographic Information Systems (GIS) approach and Inverse Distance Weighting (IDW) methods to perform a spatial and statistical analysis to explore whether exposure to PM 2.5 and PM 10 pollution, and additional factors, including the enrichment of the PM with inorganic elements, contribute to cytogenetic damage in residents living in proximity to an open-pit coal mining area. Results showed a spatial relationship between exposure to elevated concentrations of PM 2.5, PM 10 and micronuclei frequency in binucleated (MNBN) and mononucleated (MNMONO) cells. Active pits, disposal, and storage areas could be identified as the possible emission sources of combustion elements. Mining activities were also correlated with increased concentrations of highly enriched elements like S, Cu and Cr in the atmosphere, corroborating its role in the inorganic elements pollution around coal mines. Elements enriched in the PM 2.5 fraction contributed to increasing of MNBN but seems to be more related to increased MNMONO frequencies and DNA damage accumulated in vivo. The combined use of GIS and IDW methods could represent an important tool for monitoring potential cancer risk associated to dynamically distributed variables like the PM. Copyright © 2018 Elsevier Ltd. All rights reserved.

Characterization, partitioning, and potential ecological risk quantification of trace elements in coal fly ash.

PubMed

Usmani, Zeba; Kumar, Vipin

2017-06-01

Coal-based thermal power plants are the major source of power generation in India. Combustion of coal gives rise to by-products such as fly ash (FA) in huge quantities. The current study focuses on physico-chemical and mineralogical characterization and risk evaluation of FA, generated from five thermal power plants (TPPs) of India. The coal, and corresponding FA and bottom ash (BA) were further analyzed for trace elements in order to observe the enrichment and partitioning behavior of elements. The environmental risk assessment of trace elements in FA was performed in accordance with geoaccumulation index (I geo ) and potential ecological risk index (PERI). The results demonstrated that FA was enriched predominantly in SiO 2 , Al 2 O 3 , and Fe 2 O 3 along with small concentrations of CaO and MgO. The mineral phases identified in FA were quartz, mullite, hematite, and magnetite. Elemental characterization indicated that the metals were more enriched in FA as compared to coal and BA. The concentrations of trace elements, Cr, Pb, Hg, and As in FA (TPPs), varied from 12.59-24.28, 22.68-43.19, <0.0001-2.29, and 0.08-3.39 mg/kg, respectively. Maximum enrichment ratio (ER) was observed for Pb (5.21) in TPP3 FA. Hg in TPP1 showed the highest partition ratio (PR) value. I geo values for metals were mostly below zero. The PERI values indicated moderate risk from TPP4 FA and low risk from TPP1, TPP2, TPP3, and TPP5 FA to the environment, according to the threshold values provided.

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

Karayigit, A.I.; Bulut, Y.; Karayigit, G.

A total of 48 samples, feed coals (FCs), fly ashes (FAs) and bottom ashes (BAs), which were systematically collected once a week over an eight-week period from boiler units, B1-4 with 660 MW and B5-6 with 330 MW capacity from Soma power plant, have been evaluated for major and trace elements (Al, Ca, Fe, K, Mg, Mn, Na, Ti, S, As, B, Ba, Be, Bi, Cd, Co, Cr, Cu, Cs, Ga, Ge, Hf, Hg, Li, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Se, Sn, Sr, Ta, Th, Tl, U, V, Y, Zn, Zr, and REEs) to get information onmore » behavior during coal combustion. This study indicates that some elements such as Hg, Bi, Cd, As, Pb, Ge, Tl, Sn, Zn, Sb, B show enrichments in FAs relative to the BAs in both group boiler units. In addition to these, Cs, Lu, Tm, and Ga in Units B1-4 and S in Units B5-6 also have enrichments in FAs. Elements showing enrichments in BAs in both group boiler units are Ta, Mn, Nb. In addition to these, Se, Ca, Mg, Na, Fe in Units B1-4 and Cu in Units B5-6 also have enrichments in BAs. The remaining elements investigated in this study have no clear segregation between FAs and BAs. Mass balance calculations with the two methods show that some elements, S, Ta, Hg, Se, Zn, Na, Ca in Units B1-4, and Hg, S, Ta, Se, P in Units B5-6, have volatile behavior during coal combustion in the Soma power plant. This study also implies that some elements, Sb and Tb in Units B1-4 and Sb in Units B5-6, have relatively high retention effects in the combustion residues from the Soma power plant.« less

Effect of combustion temperature on the emission of trace elements under O2/CO2 atmosphere during coal combustion

NASA Astrophysics Data System (ADS)

Qu, Chengrui; Zhang, Mo; Mann, Michael. D.

2018-03-01

The effect of combustion temperature on the emission of trace elementswas studied under O2/CO2 atmosphere during coal combustion in a laboratory scale fluidized bed combustor. The elemental composition of fine fly ash particles collected with a low pressure impactor(LPI)was quantified by X-Ray F1uorescence Spectrometer (XRF). The elemental composition of coal and bottom ash was quantified byinductively coupled plasma-atomic emission spectroscopy (ICP-AES). The results indicate that the contents of Mn, Zn, Cd and Cr in the fly ash increase with the rise of combustion temperature. It is found that the enrichment of Zn and Cd is greater in the submicrometer particles than the supermicrometer particles, but Mn and Cr do not enrich in the submicrometer particles. Mn, Zn, Cd and Cr display one peak around 0.1 μm. The relative enrichment factor (Rij) of four elements is in the order of Zn, Cd, Mn and Cr. Zn and Cd are mostly retained in fly ashwhileMn and Cr are retained in both the fly ash and bottom ash.

Trace element fluxes during the last 100 years in sediment near a nuclear power plant

NASA Astrophysics Data System (ADS)

Bojórquez-Sánchez, S.; Marmolejo-Rodríguez, A. J.; Ruiz-Fernández, A. C.; Sánchez-González, A.; Sánchez-Cabeza, J. A.; Bojórquez-Leyva, H.; Pérez-Bernal, L. H.

2017-11-01

The Salada coastal lagoon is located in Veracruz (Mexico) near the Laguna Verde Nuclear Power Plant (LVNPP). Currently, the lagoon receives the cooling waters used in the LVNPP. To evaluate the fluxes and mobilization of trace elements due to human activities in the area, two sediment cores from the coastal flood plains of Salada Lagoon were analysed. Cores were collected using PVC tubes. Sediments cores were analysed every centimetre for dating (210Pb by alpha detector) and trace metal analysis using ICP-Mass Spectrometry. The dating of both sediment cores covers the period from 1900 to 2013, which includes the construction of the LVNPP (1970's). The Normalized Enrichment Factor shows enrichment of Ag, As and Cr in both sediment cores. These enrichments correspond to the extent of mining activity (which reached a maximum in the 1900's) and to the geological setting of the coastal zone. The profiles of the element fluxes in both sediment cores reflected the construction and operation of the LVNPP; however, the elements content did not show evidence of pollution coming from the LVNPP.

Internalization, separation-individuation, and the nature of therapeutic action.

PubMed

Blatt, S J; Behrends, R S

1987-01-01

Based on the assumption that the mutative factors that facilitate growth in psychoanalysis involve the same fundamental mechanisms that lead to psychological growth in normal development, this paper considers the constant oscillation between gratification and deprivation leading to internalization as the central therapeutic mechanism of the psychoanalytic process. Patients experience the analytic process as a series of gratifying involvements and experienced incompatibilities that facilitate internalization, whereby the patient recovers lost or disrupted regulatory, gratifying interactions with the analyst, which are real or fantasied, by appropriating these interactions, transforming them into their own, enduring, self-generated functions and characteristics. Patients internalize not only the analyst's interpretive activity, but also the analyst's sensitivity, compassion and acceptance, and, in addition, their own activity in relation to the analyst such as free association. Both interpretation and the therapeutic relationship can contain elements of gratifying involvement and experienced incompatibility that lead to internalization and therefore both can be mutative factors in the therapeutic process.

Early Paleozoic dioritic and granitic plutons in the Eastern Tianshan Orogenic Belt, NW China: Constraints on the initiation of a magmatic arc in the southern Central Asian Orogenic Belt

NASA Astrophysics Data System (ADS)

Du, Long; Long, Xiaoping; Yuan, Chao; Zhang, Yunying; Huang, Zongying; Sun, Min; Zhao, Guochun; Xiao, Wenjiao

2018-03-01

Early Paleozoic dioritic and granitic plutons in the Eastern Tianshan Orogenic Belt (ETOB) have been studied in order to constraint the initiation of a magmatic arc formed in this region. Zircon U-Pb dating indicates that two dioritic plutons in the northern ETOB were generated in the Late Ordovician (452 ± 4 Ma) and the Early Silurian (442 ± 3 Ma), respectively. Diorites from the two plutons are characterized by enrichments in large ion lithophile elements (LILE) and highly incompatible elements, with depletions in high field strength elements (HSFE) displaying typical geochemical features of a subduction-related origin. They have positive εNd(t) values (+5.08-+6.58), relatively young Nd model ages (TDM = 0.71-1.08 Ga), with Ta/Yb (0.05-0.09) and Nb/Ta ratios (12.06-15.19) similar to those of depleted mantle, suggesting a juvenile mantle origin. Their high Ba/La (13.3-35.9), low Th/Yb (0.72-2.02), and relatively low Ce/Th (4.57-14.7) and Ba/Th (47.8-235) ratios indicate that these diorites were probably produced by partial melting of a depleted mantle wedge metasomatized by both subducted sediment-derived melts and slab-derived aqueous fluids. Zircon U-Pb dating of a granitic pluton in the northern ETOB yielded a Late Ordovician intrusion age of 447 ± 5 Ma. Granites from this pluton show calc-alkaline compositions with geochemical characteristics of I-type granites. They also show positive εNd(t) values (+6.49-+6.95) and young Nd model ages (TDM = 0.69-0.87 Ga), indicating that the granites were most likely derived from juvenile lower crust. Our new dating results on the dioritic and granitic plutons suggest that arc-type magmatism in the northern ETOB began prior to or at the Late Ordovician (452-442 Ma). In addition, north-dipping subduction of the Kangguertage oceanic lithosphere may account for the arc-type magmatism and the geodynamic process of the ETOB in the Early Paleozoic.

Dacite petrogenesis on mid-ocean ridges: Evidence for oceanic crustal melting and assimilation

USGS Publications Warehouse

Wanless, V.D.; Perfit, M.R.; Ridley, W.I.; Klein, E.

2010-01-01

Whereas the majority of eruptions at oceanic spreading centers produce lavas with relatively homogeneous mid-ocean ridge basalt (MORB) compositions, the formation of tholeiitic andesites and dacites at mid-ocean ridges (MORs) is a petrological enigma. Eruptions of MOR high-silica lavas are typically associated with ridge discontinuities and have produced regionally significant volumes of lava. Andesites and dacites have been observed and sampled at several locations along the global MOR system; these include propagating ridge tips at ridge-transform intersections on the Juan de Fuca Ridge and eastern Gal??pagos spreading center, and at the 9??N overlapping spreading center on the East Pacific Rise. Despite the formation of these lavas at various ridges, MOR dacites show remarkably similar major element trends and incompatible trace element enrichments, suggesting that similar processes are controlling their chemistry. Although most geochemical variability in MOR basalts is consistent with low-pressure fractional crystallization of various mantle-derived parental melts, our geochemical data for MOR dacitic glasses suggest that contamination from a seawater-altered component is important in their petrogenesis. MOR dacites are characterized by elevated U, Th, Zr, and Hf, low Nb and Ta concentrations relative to rare earth elements (REE), and Al2O3, K2O, and Cl concentrations that are higher than expected from low-pressure fractional crystallization alone. Petrological modeling of MOR dacites suggests that partial melting and assimilation are both integral to their petrogenesis. Extensive fractional crystallization of a MORB parent combined with partial melting and assimilation of amphibole-bearing altered crust produces a magma with a geochemical signature similar to a MOR dacite. This supports the hypothesis that crustal assimilation is an important process in the formation of highly evolved MOR lavas and may be significant in the generation of evolved MORB in general. Additionally, these processes are likely to be more common in regions of episodic magma supply and enhanced magma-crust interaction such as at the ends of ridge segments. ?? The Author 2010. Published by Oxford University Press. All rights reserved.

Occurrence of high-Al N-MORB along the Easternmost Southwest Indian Ridge

NASA Astrophysics Data System (ADS)

Meyzen, C. M.; Humler, E.; Ludden, J. N.

2017-12-01

One of the deepest and slowest part of the mid-ocean-ridge system lies within the easternmost part of the Southwest Indian Ridge between 61°E and 69° E. In this region, a distinctive sea-floor terrain characterized by high-relief segments separated by long, deep tectonized sections shows a predominance of tectonic over magmatic extensional processes, suggesting an unstable and weak, but locally focalized magma supply. Other features of this section include the absence of long-lived transforms, thick lithosphere, high upper mantle seismic wave velocities and thin oceanic crust (4-5 km). When compared to other ridge segments, most MORB erupted along this section distinguish themselves by their higher Na2O, Sr and Al2O3 compositions, very low CaO/Al2O3 ratios relative to TiO2 and depleted heavy rare-earth element (REE) distributions. Another peculiar feature is their subparallel LREE enriched patterns. The high-Al-MgO magma type erupted periodically around the ridge system is also found in this region at 61.93°E. These lavas are characterized by high Al2O3 (> 17 wt. %), MgO (> 8.8 wt. %) and FeO contents, low SiO2 (< 49 wt. %) and Na2O and very low TiO2 (< 1 wt. %), and a LREE depleted pattern compared to the main population. At slightly lower MgO, sporadically, two other dredges located at 63.36-63.66°E share some of these distinct compositional characteristics. As a whole, these lavas are the most depleted in highly incompatible elements, but are also characterized by an offset toward lower MREE/HREE ratios relative to the main population. These peculiar basalts are not parental to the more common lower MgO compositions and cannot be related to them by fractional crystallization alone. Instead, their major element features, and the occasional presence of positive Eu and Sr anomalies might indicate assimilation of plagioclase cumulates, while their offset in MREE/HREE might require a multistage melting evolution with an earlier event in the garnet stability field.

Diverse lavas from closely spaced volcanoes drawing from a common parent: Emmons Lake Volcanic Center, Eastern Aleutian Arc

USGS Publications Warehouse

Mangan, M.; Miller, T.; Waythomas, C.; Trusdell, F.; Calvert, A.; Layer, P.

2009-01-01

Emmons Lake Volcanic Center (ELVC) on the lower Alaskan Peninsula is one of the largest and most diverse volcanic centers in the Aleutian Arc. Since the Middle Pleistocene, eruption of ~ 350 km3 of basalt through rhyolite has produced a 30 km, arc front chain of nested calderas and overlapping stratovolcanoes. ELVC has experienced as many as five major caldera-forming eruptions, the most recent, at ~ 27 ka, produced ~ 50 km3 of rhyolitic ignimbrite and ash fall. These violent silicic events were interspersed with less energetic, but prodigious, outpourings of basalt through dacite. Holocene eruptions are mostly basaltic andesite to andesite and historically recorded activity includes over 40 eruptions within the last 200 yr, all from Pavlof volcano, the most active site in the Aleutian Arc. Geochemical and geophysical observations suggest that although all ELVC eruptions derive from a common clinopyroxene + spinel + plagioclase fractionating high-aluminum basalt parent in the lower crust, magma follows one of two closely spaced, but distinct paths to the surface. Under the eastern end of the chain, magma moves rapidly and cleanly through a relatively young (~ 28 ka), hydraulically connected dike plexus. Steady supply, short magma residence times, and limited interaction with crustal rocks preserve the geochemistry of deep crustal processes. Below the western part of the chain, magma moves haltingly through a long-lived (~ 500 ka) and complex intrusive column in which many generations of basaltic to andesitic melts have mingled and fractionated. Buoyant, silicic melts periodically separate from the lower parts of the column to feed voluminous eruptions of dacite and rhyolite. Mafic lavas record a complicated passage through cumulate zones and hydrous silicic residues as manifested by disequilibrium phenocryst textures, incompatible element enrichments, and decoupling of REEs and HFSEs ratios. Such features are absent in mafic lavas from the younger part of the chain, highlighting the importance of plumbing architecture and longevity in creating petrologic diversity. Supplemental Data include 156 major element (XRF) and 128 trace element (ICP-MS) whole-rock analyses, 23 new 40Ar/39Ar ages, a generalized geologic map with associated unit descriptions and field photographs, and photomicrographs of key petrographic features.

The unusual mineralogy of the Hayes River rhyolite, Hayes Volcano, Cook Inlet, Alaska

NASA Astrophysics Data System (ADS)

Hayden, L. A.; Coombs, M. L.; McHugh, K.

2013-12-01

Hayes Volcano is an ice-covered volcanic massif located in the northern Cook Inlet region approximately 135 miles northwest of Anchorage, Alaska. The last major eruptive episode of Hayes, and the only known in any detail, occurred ~3,700 yr B.P. and produced the Hayes Tephra Set H, a series of dacitic fall deposits widespread throughout southcentral Alaska (Riehle et al., 1994, Quat. Res. 33, p. 91-108). An undated, early Holocene pyroclastic-flow deposit exposed beneath Tephra Set H in the Hayes River valley is unusual in the Aleutian-Alaska subduction zone in whole-rock composition and mineralogy. The deposit comprises rhyolite pumice (~75 wt% SiO2) that contain phenocrysts of plagioclase, sanidine, quartz, and biotite in vesicular, clear matrix glass, and <1% dense, white cognate inclusions with the same whole-rock composition and phenocryst assemblage as the pumice, but a crystalline matrix. Holocrystalline inclusions may represent portions of the magma body that rapidly quenched in the shallow subsurface as dikes or chamber rinds and were then excavated during explosive eruption. Rhyolite and inclusions are peraluminous (2-3 % normative corundum), high-K, enriched in incompatible elements, and depleted in Sr and Eu. In accord with its evolved and enriched composition the rhyolite pumice and inclusions contain an abundance of accessory phases, including apatite, monazite, xenotime, and zircon. Monazite are euhedral, as large as 500 um, ThO2-rich (up to 4 wt%) and contain significant amounts of Ag (200-500 ppm). Xenotime are generally smaller than the monazite and occur frequently as small blebs. Rhyolite pumices also contain Fe-sulfides, Cu, Sn, Ni, and barite. Sanidine phenocrysts in the pumice and inclusions are sharply zoned and highly enriched in the celsian component (up to 5 wt% BaO) and also show LREE enrichment. Inclusions contain abundant Mn-rich cordierite (~3 wt% Mn2O3) in the san-plag-qtz matrix, as well as Fe-Ti oxides that are relatively high in Mn2O3 (>1 wt%) and REE-enriched. Zircon saturation temperatures (716° C) and two-feldspar thermometry (630-700° C for phenocryst rims; 660° C for inclusion matrix microphenocrysts) suggest a cool magma that must have been volatile-rich given its relatively low phenocryst content (~25 %). A lack of crustal xenocrysts, and Pb, Sr, and Nd isotopes similar to other Cook Inlet volcanoes (McHugh et al., 2012 Fall AGU, V31A-2760) suggest that the rhyolite is not a crustal melt, and we suggest that it formed by low degrees of melting or high degree of crystallization of mafic arc-related rocks. At Hayes, concentrations of REE and metals resulted from extreme fractionation process(es), which active over extended time period may lead to the formation of mineral deposits.

Modes of occurrence of mercury and other trace elements in coals from the warrior field, Black Warrior Basin, Northwestern Alabama

USGS Publications Warehouse

Diehl, S.F.; Goldhaber, M.B.; Hatch, J.R.

2004-01-01

The mineralogic residence and abundance of trace metals is an important environmental issue. Data from the USGS coal quality database show that potentially toxic elements, including Hg, As, Mo, Se, Cu, and Tl are enriched in a subset of coal samples in the Black Warrior Basin of Alabama, USA. Although the coal as-mined typically is low in these elements, localized enrichments occur in high-pyrite coals and near faults. Microscopic analyses demonstrate that the residence of these elements is dominantly in a late-stage pyrite associated with structurally disrupted coal. Further, our data suggest addition of Hg to the coal matrix as well. The source of these trace elements was hydrothermal fluids driven into the Black Warrior Basin by Alleghanian age tectonism. ?? 2004 Published by Elsevier B.V.

Apollo 16: a trace element perspective

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

Jovanovic, S.; Reed, G.W. Jr.

1980-01-01

A brief summary of some inferences regarding the Apollo 16 site that can be arrived at from incompatible element-geochemical data is presented. We use a set of elements not exploited to address some of the questions about the geology of the Apollo 16 site and the evolution of the highlands crust. Others have recognized the great difficulty in disentangling the complex history of the highlands on the basis of petrographic and compositional data. We have previously attempted to reconcile a relatively few interelement relationships with information from many other sources. The Apollo 16 site and the significance of Apollo 16more » samples have been examined from the perspectives of data on Cl, P, Ru and Os for the most part and also, in a few cases, data on the heavy metals Pb, Tl and Bi.« less

Influence of soil chemistry on metal and bioessential element concentrations in nymphal and adult periodical cicadas (Magicicada spp.).

PubMed

Robinson, G R; Sibrell, P L; Boughton, C J; Yang, L H

2007-03-15

Metal and bioessential element concentrations were measured in three species of 17-year periodical cicadas (Magicicada spp.) to determine how cicada tissue chemistry is affected by soil chemistry, measure the bioavailability of metals from both uncontaminated and lead-arsenate-pesticide contaminated soils, and assess the potential risks of observed metal contamination for wildlife. Periodical cicada nymphs feed on root xylem fluids for 13 or 17 years of underground development. The nymphs then emerge synchronously at high densities, before leaving their nymphal keratin exoskeleton and molting into their adult form. Cicadas are an important food source for birds and animals during emergence events, and influence nutrient cycles in woodland ecosystems. Nymphal exoskeletons and whole adult cicadas were sampled in Clarke and Frederick Counties, Virginia and Berkeley and Jefferson Counties, West Virginia during the Brood X emergence in May and June, 2004. Elements, such as Al, Fe, and Pb, are strongly enriched in the nymphal exoskeleton relative to the adult body; Cu and Zn are enriched in bodies. Concentrations of Fe and Pb, when normalized to relatively inert soil constituents such as Al and Ce, are similar in both the molt exoskeleton and their host soil, implying that passive assimilation through prolonged soil contact (adhesion or adsorption) might control these metal concentrations. Normalized concentrations of bioessential elements, such as S, P, K, Ca, Mn, Cu, Zn, and Mo, and chalcophile (sulfur-loving) elements, such as As, Se, and Au, indicate strong enrichment in cicada tissues relative to soil, implying selective absorption and retention by xylem fluids, the cicada nymphs themselves, or both. Element enrichment patterns in cicada tissues are similar to enrichment patterns observed in xylem fluids from tree roots. Chalcophile elements and heavy metals accumulate in keratin-rich tissues and may bind to sulfhydryl groups. Metal concentrations in the nymphal exoskeleton show a positive correlation with soil metal concentrations, with Au exhibiting particularly strong enrichment in the exoskeleton relative to soil concentrations. Metal concentrations in adult bodies do not correlate with soil chemistry. Bioessential elements S, Ca, Mn, Fe, and Zn differed by sex in adults, whereas Na, Mg, K, Ca, Mn, Fe, Zn, and As differed by species. Body concentrations of Ca differed by site conditions (orchard or reference setting). The high Pb contents of orchard soils contaminated by arsenical pesticide residues might inhibit Ca uptake by cicada nymphs. The adult cicadas contain concentrations of metals similar to, or less than, other invertebrates, such as earthworms. There does not appear to be a dietary threat to birds or other consumers of adult cicadas based on Maximum Tolerable Dietary Level (MTDL) Guidelines developed for agricultural animals.

Influence of soil chemistry on metal and bioessential element concentrations in nymphal and adult periodical cicadas (Magicicada spp.)

USGS Publications Warehouse

Robinson, G.R.; Sibrell, P.L.; Boughton, C.J.; Yang, L.H.

2007-01-01

Metal and bioessential element concentrations were measured in three species of 17-year periodical cicadas (Magicicada spp.) to determine how cicada tissue chemistry is affected by soil chemistry, measure the bioavailability of metals from both uncontaminated and lead-arsenate-pesticide contaminated soils, and assess the potential risks of observed metal contamination for wildlife. Periodical cicada nymphs feed on root xylem fluids for 13 or 17??years of underground development. The nymphs then emerge synchronously at high densities, before leaving their nymphal keratin exoskeleton and molting into their adult form. Cicadas are an important food source for birds and animals during emergence events, and influence nutrient cycles in woodland ecosystems. Nymphal exoskeletons and whole adult cicadas were sampled in Clarke and Frederick Counties, Virginia and Berkeley and Jefferson Counties, West Virginia during the Brood X emergence in May and June, 2004. Elements, such as Al, Fe, and Pb, are strongly enriched in the nymphal exoskeleton relative to the adult body; Cu and Zn are enriched in bodies. Concentrations of Fe and Pb, when normalized to relatively inert soil constituents such as Al and Ce, are similar in both the molt exoskeleton and their host soil, implying that passive assimilation through prolonged soil contact (adhesion or adsorption) might control these metal concentrations. Normalized concentrations of bioessential elements, such as S, P, K, Ca, Mn, Cu, Zn, and Mo, and chalcophile (sulfur-loving) elements, such as As, Se, and Au, indicate strong enrichment in cicada tissues relative to soil, implying selective absorption and retention by xylem fluids, the cicada nymphs themselves, or both. Element enrichment patterns in cicada tissues are similar to enrichment patterns observed in xylem fluids from tree roots. Chalcophile elements and heavy metals accumulate in keratin-rich tissues and may bind to sulfhydryl groups. Metal concentrations in the nymphal exoskeleton show a positive correlation with soil metal concentrations, with Au exhibiting particularly strong enrichment in the exoskeleton relative to soil concentrations. Metal concentrations in adult bodies do not correlate with soil chemistry. Bioessential elements S, Ca, Mn, Fe, and Zn differed by sex in adults, whereas Na, Mg, K, Ca, Mn, Fe, Zn, and As differed by species. Body concentrations of Ca differed by site conditions (orchard or reference setting). The high Pb contents of orchard soils contaminated by arsenical pesticide residues might inhibit Ca uptake by cicada nymphs. The adult cicadas contain concentrations of metals similar to, or less than, other invertebrates, such as earthworms. There does not appear to be a dietary threat to birds or other consumers of adult cicadas based on Maximum Tolerable Dietary Level (MTDL) Guidelines developed for agricultural animals.

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

High-throughput simultaneous determination of plasma water deuterium and 18-oxygen enrichment using a high-temperature conversion elemental analyzer with isotope ratio mass spectrometry.

PubMed

Richelle, M; Darimont, C; Piguet-Welsch, C; Fay, L B

2004-01-01

This paper presents a high-throughput method for the simultaneous determination of deuterium and oxygen-18 (18O) enrichment of water samples isolated from blood. This analytical method enables rapid and simple determination of these enrichments of microgram quantities of water. Water is converted into hydrogen and carbon monoxide gases by the use of a high-temperature conversion elemental analyzer (TC-EA), that are then transferred on-line into the isotope ratio mass spectrometer. Accuracy determined with the standard light Antartic precipitation (SLAP) and Greenland ice sheet precipitation (GISP) is reliable for deuterium and 18O enrichments. The range of linearity is from 0 up to 0.09 atom percent excess (APE, i.e. -78 up to 5725 delta per mil (dpm)) for deuterium enrichment and from 0 up to 0.17 APE (-11 up to 890 dpm) for 18O enrichment. Memory effects do exist but can be avoided by analyzing the biological samples in quintuplet. This method allows the determination of 1440 samples per week, i.e. 288 biological samples per week. Copyright 2004 John Wiley & Sons, Ltd.

Sub-Micrometer Scale Minor Element Mapping in Interplanetary Dust Particles: A Test for Stratospheric Contamination

NASA Technical Reports Server (NTRS)

Flynn, G. J.; Keller, L. P.; Sutton, S. R.

2004-01-01

Combined X-ray microprobe (XRM), energy dispersive x-ray fluorescence using a Transmission Electron Microscope (TEM), and electron microprobe measurements have determined that the average bulk chemical composition of the interplanetary dust particles (IDPs) collected from the Earth s stratosphere is enriched relative to the CI meteorite composition by a factor of 2 to 4 for carbon and for the moderately volatile elements Na, K, P, Mn, Cu, Zn, Ga, Ge, and Se, and enriched to approximately 30 times CI for Br. However, Jessberger et al., who have reported similar bulk enrichments using Proton Induced X-ray Emission (PIXE), attribute the enrichments to contamination by meteor-derived atmospheric aerosols during the several weeks these IDPs reside in the Earth s atmosphere prior to collection. Using scanning Auger spectroscopy, a very sensitive surface analysis technique, Mackinnon and Mogk have observed S contamination on the surface of IDPs, presumably due to the accretion of sulfate aerosols during stratospheric residence. But the S-rich layer they detected was so thin (approximately 100 angstroms thick) that the total amount of S on the surface was too small to significantly perturb the bulk S-content of a chondritic IDP. Stephan et al. provide support for the contamination hypothesis by reporting the enrichment of Br on the edges of the IDPs using Time-of-Flight Secondary-Ion Mass-Spectrometry (TOFSIMS), but TOF-SIMS is notorious for producing false edge-effects, particularly on irregularly-shaped samples like IDPs. Sutton et al. mapped the spatial distribution of Fe, Ni, Zn, Br, and Sr, at the approximately 2 m scale, in four IDPs using element-specific x-ray fluorescence (XRF) computed microtomography. They found the moderately volatile elements Zn and Br, although spatially inhomogeneous, were not concentrated on the surface of any of the IDPs they examined, suggesting that the Zn and the Br enrichments in the IDPs are not due to contamination during stratospheric residence.

Soil geochemical signature of urbanization and industrialization – Chicago, Illinois, USA

USGS Publications Warehouse

Cannon, W.F.; Horton, John D.

2009-01-01

The concentrations of 45 elements in ambient (not obviously disturbed) surface soils were determined for 57 sites distributed throughout the city of Chicago, Illinois in the upper Midwestern United States. These concentrations were compared to soils from 105 sites from a largely agricultural region within a 500-km radius surrounding the city and to soils collected from 90 sites across the state of Illinois. Although the bulk composition of the Chicago urban soils reflects largely natural sources, the soils are significantly enriched in many trace elements, apparently from anthropogenic sources. The median concentration of Pb in Chicago soils is 198 mg/kg, a 13-fold enrichment compared to regional concentrations. Zinc (median 235 mg/kg), Cu (59 mg/kg), and Ni (31 mg/kg) are also enriched from 2- to 4-fold in Chicago soils and all four elements show strong mutual correlations. These elevated concentrations are most likely related to vehicular and roadway sources and represent uneven distribution across the city as airborne material. Other airborne particulate material from a combination of fossil fuel combustion, waste incineration, and steel production may contribute to apparent elevated concentrations in Chicago soil of Fe (median 2.9%), Mo (5 mg/kg), V (82 mg/kg) and S (0.09%). Chicago soils are enriched from about 1.6- to 3-fold in these elements. Enrichments in P and Se may be caused by direct addition of phosphate fertilizer to parklands, lawns and gardens. The density of the sampling (1 site per 10 km2) is inadequate to define the distribution of the observed enrichments within the city or to predict soil compositions for most of the areas between sample sites, but does provide a statistically significant signature of the history of urban and industrial activity within the city in contrast to the surrounding agricultural lands.

Timescale of Petrogenetic Processes Recorded in the Mount Perkins Magma System, Northern Colorado River Extension Corridor, Arizona

NASA Technical Reports Server (NTRS)

Danielson, Lisa R.; Metcalf, Rodney V.; Miller, Calvin F.; Rhodes Gregory T.; Wooden, J. L.

2013-01-01

The Miocene Mt. Perkins Pluton is a small composite intrusive body emplaced in the shallow crust as four separate phases during the earliest stages of crustal extension. Phase 1 (oldest) consists of isotropic hornblende gabbro and a layered cumulate sequence. Phase 2 consists of quartz monzonite to quartz monzodiorite hosting mafic microgranitoid enclaves. Phase 3 is composed of quartz monzonite and is subdivided into mafic enclave-rich zones and enclave-free zones. Phase 4 consists of aphanitic dikes of mafic, intermediate and felsic compositions hosting mafic enclaves. Phases 2-4 enclaves record significant isotopic disequilibrium with surrounding granitoid host rocks, but collectively enclaves and host rocks form a cogenetic suite exhibiting systematic variations in Nd-Sr-Pb isotopes that correlate with major and trace elements. Phases 2-4 record multiple episodes of magma mingling among cogenetic hybrid magmas that formed via magma mixing and fractional crystallization at a deeper crustal. The mafic end-member was alkali basalt similar to nearby 6-4 Ma basalt with enriched OIB-like trace elements and Nd-Sr-Pb isotopes. The felsic end-member was a subalkaline crustal-derived magma. Phase 1 isotropic gabbro exhibits elemental and isotopic compositional variations at relatively constant SiO2, suggesting generation of isotropic gabbro by an open-system process involving two mafic end-members. One end-member is similar in composition to the OIB-like mafic end-member for phases 2-4; the second is similar to nearby 11-8 Ma tholeiite basalt exhibiting low epsilon (sub Nd), and depleted incompatible trace elements. Phase 1 cumulates record in situ fractional crystallization of an OIB-like mafic magma with isotopic evidence of crustal contamination by partial melts generated in adjacent Proterozoic gneiss. The Mt Perkins pluton records a complex history in a lithospheric scale magma system involving two distinct mantle-derived mafic magmas and felsic magma sourced in the crust. Mixing and fractional crystallization of these magmas at various levels in the crust generated a suite of intermediate composition magmas. U-Pb zircon SHRIMP ages of phase 1 (15.7 +/- 0.2 Ma), phase 3 (15.8 +/- 0.2 Ma) and phase 4 (15.4 +/- 0.3 Ma) document a 100-300k year timescale for petrogenetic processes recorded in the Mt Perkins magma system.

Generation of high-Mg andesites in the Kueishantao volcano, the southernmost part of the Okinawa Trough

NASA Astrophysics Data System (ADS)

Chu, C.; Chung, S.; Shinjo, R.; Wang, S.; Chen, C.

2004-12-01

Kueishantao is an emerged volcanic islet located at the western end of the Southernmost Part of Okinawa Trough (SPOT). The Okinawa Trough, extending from SW Kyushu, Japan to NE Taiwan, is widely regarded as a backarc basin that is built behind the Ryukyu arc-trench system owing to subduction of the Philippine Sea plate underneath the Eurasian plate. The SPOT, however, is not a simple backarc basin but an embryonic rift zone in which early arc volcanism occurs as a result of the Ryukyu subduction (Chung et al., 2000). The Kueishantao is one of such volcanoes thus formed in the SPOT and consists mainly of andesitic lava flows dated to be ˜7000 yr old. In this study, we report whole rock major and trace element, and Sr-Nd-Pb isotope compositions of the Kueishantao andesites. The results indicate that some of the samples have unexpectedly high magnesium, with MgO ≥ 5 wt.% and Mg# > 0.5, relative to their silica contents (SiO2≈ 60 wt.%), which allow them to be coined as high-Mg andesites (HMAs). In the incompatible element variation diagram, these Kueishantao HMAs exhibit enrichments in the large ion lithophile elements and Th, U and Pb, and depletions in the high field strength elements, features typical of arc lavas from the Ryukyu subduction zone as well as convergent margins worldwide. More interestingly, their overall geochemical compositions are very similar to those of the mean continental crust proposed by Rudnick and Fountain (1995). The Kueishantao HMAs have uniform isotope compositions, with low ɛ Nd (-4.3 to -5.0), high Sr (87Sr/86Sr¡Ö≈ 0.706) and Pb (18.75, 15.68 and 39.02 of 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb, respectively) ratios. Such ¡°continental¡± isotopic signatures have led previous workers (Chen et al., 1995) to argue significant crustal contamination as a major petrogenetic process, but our evaluation shows that this simple binary mixing model fails to explain their geochemical and Pb isotope systematics. We propose, instead, that the Kueishantao HMAs result from partial melting of subducting sediments and subsequent melt-mantle interaction, an interpretation in consistency with seismic tomographic data beneath the SPOT characterized by a complex collision/extension/subduction tectonic context off NE Taiwan.

Combining raw and compositional data to determine the spatial patterns of Potentially Toxic Elements in soils.

PubMed

Boente, C; Albuquerque, M T D; Fernández-Braña, A; Gerassis, S; Sierra, C; Gallego, J R

2018-08-01

When considering complex scenarios involving several attributes, such as in environmental characterization, a clearer picture of reality can be achieved through the dimensional reduction of data. In this context, maps facilitate the visualization of spatial patterns of contaminant distribution and the identification of enriched areas. A set, of 15 Potentially Toxic Elements (PTEs) - (As, Ba, Cd, Co, Cr, Cu, Hg, Mo, Ni, Pb, Sb, Se, Tl, V, and Zn), was measured in soil, collected in Langreo's municipality (80km 2 ), Spain. Relative enrichment (RE) is introduced here to refer to the proportion of elements present in a given context. Indeed, a novel approach is provided for research into PTE fate. This method involves studying the variability of PTE proportions throughout the study area, thereby allowing the identification of dissemination trends. Traditional geostatistical approaches commonly use raw data (concentrations) accepting that the elements analyzed make up the entirety of the soil. However, in geochemical studies the analyzed elements are just a fraction of the total soil composition. Therefore, considering compositional data is pivotal. The spatial characterization of PTEs considering raw and compositional data together allowed a broad discussion about, not only the PTEs concentration's distribution but also to reckon possible trends of relative enrichment (RE). Transformations to open closed data are widely used for this purpose. Spatial patterns have an indubitable interest. In this study, the Centered Log-ratio transformation (clr) was used, followed by its back-transformation, to build a set of compositional data that, combined with raw data, allowed to establish the sources of the PTEs and trends of spatial dissemination. Based on the obtained findings it was possible to conclude that the Langreo area is deeply affected by its industrial and mining legacy. City center is highly enriched in Pb and Hg and As shows enrichment in a northwesterly direction. Copyright © 2018 Elsevier B.V. All rights reserved.

Quantifying Volcanic Emissions of Trace Elements to the Atmosphere: Ideas Based on Past Studies

NASA Astrophysics Data System (ADS)

Rose, W. I.

2003-12-01

Extensive data exist from volcanological and geochemical studies about exotic elemental enrichments in volcanic emissions to the atmosphere but quantitative data are quite rare. Advanced, highly sensitive techniques of analysis are needed to detect low concentrations of some minor elements, especially during major eruptions. I will present data from studies done during low levels of activity (incrustations and silica tube sublimates at high temperature fumaroles, from SEM studies of particle samples collected in volcanic plumes and volcanic clouds, from geochemical analysis of volcanic gas condensates, from analysis of treated particle and gas filter packs) and a much smaller number that could reflect explosive activity (from fresh ashfall leachate geochemistry, and from thermodynamic codes modeling volatile emissions from magma). This data describes a highly variable pattern of elemental enrichments which are difficult to quantify, generalize and understand. Sampling in a routine way is difficult, and work in active craters has heightened our awareness of danger, which appropriately inhibits some sampling. There are numerous localized enrichments of minor elements that can be documented and others can be expected or inferred. There is a lack of systematic tools to measure minor element abundances in volcanic emissions. The careful combination of several methodologies listed above for the same volcanic vents can provide redundant data on multiple elements which could lead to overall quantification of minor element fluxes but there are challenging issues about detection. For quiescent plumes we can design combinations of measurements to quantify minor element emission rates. Doing a comparable methodology to succeed in measuring minor element fluxes for significant eruptions will require new strategies and/or ideas.

Seasonal Dynamics of Trace Elements in Tidal Salt Marsh Soils as Affected by the Flow-Sediment Regulation Regime

PubMed Central

Bai, Junhong; Xiao, Rong; Zhao, Qingqing; Lu, Qiongqiong; Wang, Junjing; Reddy, K. Ramesh

2014-01-01

Soil profiles were collected in three salt marshes with different plant species (i.e. Phragmites australis, Tamarix chinensis and Suaeda salsa) in the Yellow River Delta (YRD) of China during three seasons (summer and fall of 2007 and the following spring of 2008) after the flow-sediment regulation regime. Total elemental contents of As, Cd, Cu, Pb and Zn were determined using inductively coupled plasma atomic absorption spectrometry to investigate temporal variations in trace elements in soil profiles of the three salt marshes, assess the enrichment levels and ecological risks of these trace elements in three sampling seasons and identify their influencing factors. Trace elements did not change significantly along soil profiles at each site in each sampling season. The highest value for each sampling site was observed in summer and the lowest one in fall. Soils in both P. australis and S. salsa wetlands tended to have higher trace element levels than those in T. chinensis wetland. Compared to other elements, both Cd and As had higher enrichment factors exceeding moderate enrichment levels. However, the toxic unit (TU) values of these trace elements did not exceed probable effect levels. Correlation analysis showed that these trace elements were closely linked to soil properties such as moisture, sulfur, salinity, soil organic matter, soil texture and pH values. Principal component analysis showed that the sampling season affected by the flow-sediment regulation regime was the dominant factor influencing the distribution patterns of these trace elements in soils, and plant community type was another important factor. The findings of this study could contribute to wetland conservation and management in coastal regions affected by the hydrological engineering. PMID:25216278

New Ages for Gorgona Island, Colombia: Implications for Previous Petrogenetic and Tectonic Models

NASA Astrophysics Data System (ADS)

Serrano Duran, L.; Lopez Martinez, M.; Ferrari, L.

2007-05-01

The Gorgona Island, located 50 km to the west of the Colombian Pacific coast, is the only known site with Phanerozoic komatiites in the world besides a key element in several reconstruction of the interaction between the Caribbean and the South America Plate. The Gorgona komatiites are part of an igneous complex that also includes picritic basalts and breccias, gabbros and peridotites (dunites and wherlites), and is covered by deformed mid-Eocene and younger underformed marine sediments. Datings of the igneous rocks were only performed on basalts and include an 86 Ma K-Ar age, an 88.9 ± 1.2 Ma weighted mean of four Ar-Ar ages and an 89.2 ± 5.2 Ma Re-Os isochron age from basalts. Gorgona rocks are affected by reverse faulting with a general eastward vergence. The island is the only subaerially exposed part of a NE elongated sliver accreted in a dextral transpressional regime to the South America continental margin between the Late Eocene and the Early Miocene. Petrologic studies found large spread in radiogenic isotopes and incompatible trace element ratios in Gorgona ultramafic rocks, which have been interpreted as requiring at least two different sources of: 1) a depleted mantle responsible for the generation of the komatiites and most basalts, and 2) an enriched mantle responsible for some rarer enriched basalts and picrites. Despite the large compositional and isotopic heterogeneity the most common interpretation is that the Gorgona ultramafic rocks are the product of a single mantle plume, although it has recently proposed that this would be a separate plume from that generating the bulk of the Caribbean plateau at ~90 Ma. Our new study focused on the geochronology of the Gorgona igneous suite as we consider that this tectonically and petrologically complex island is unlike to have such a narrow age range. We attempted to date eight samples of komatiites, basalts and gabbros by Ar-Ar laser step heating. For four of these samples we successfully obtain reliable plateau and/or isochron ages. Only one basaltic sample, located in the western coast, yielded an age comparable with those previously reported in the literature. For two basalts intercalated with komatiites and a gabbro exposed in the north-eastern coast of the island we obtained younger ages, similar to those reported for some mafic and ultramafic rocks along the Pacific coast of Colombia. The two sets of ages for the ultramafic suite of Gorgona also correspond to different petrologic types. The depleted rocks in the eastern coast are younger than the enriched basalts and picrites located in the southern and western part of the island with ages around 90 Ma, suggesting a more complex tectonic evolution with the accretion of at least two different blocks. This eventually questions the "single plume" model for the formation of the Gorgona Island plateau.

Biparental chloroplast inheritance leads to rescue from cytonuclear incompatibility.

PubMed

Barnard-Kubow, Karen B; McCoy, Morgan A; Galloway, Laura F

2017-02-01

Although organelle inheritance is predominantly maternal across animals and plants, biparental chloroplast inheritance has arisen multiple times in the angiosperms. Biparental inheritance has the potential to impact the evolutionary dynamics of cytonuclear incompatibility, interactions between nuclear and organelle genomes that are proposed to be among the earliest types of genetic incompatibility to arise in speciation. We examine the interplay between biparental inheritance and cytonuclear incompatibility in Campanulastrum americanum, a plant species exhibiting both traits. We first determine patterns of chloroplast inheritance in genetically similar and divergent crosses, and then associate inheritance with hybrid survival across multiple generations. There is substantial biparental inheritance in C. americanum. The frequency of biparental inheritance is greater in divergent crosses and in the presence of cytonuclear incompatibility. Biparental inheritance helps to mitigate cytonuclear incompatibility, leading to increased fitness of F 1 hybrids and recovery in the F 2 generation. This study demonstrates the potential for biparental chloroplast inheritance to rescue cytonuclear compatibility, reducing cytonuclear incompatibility's contribution to reproductive isolation and potentially slowing speciation. The efficacy of rescue depended upon the strength of incompatibility, with a greater persistence of weak incompatibilities in later generations. These findings suggest that incompatible plastids may lead to selection for biparental inheritance. © 2016 The Authors. New Phytologist © 2016 New Phytologist Trust.

Trace- and rare-earth element geochemistry and Pb-Pb dating of black shales and intercalated Ni-Mo-PGE-Au sulfide ores in Lower Cambrian strata, Yangtze Platform, South China

NASA Astrophysics Data System (ADS)

Jiang, Shao-Yong; Chen, Yong-Quan; Ling, Hong-Fei; Yang, Jing-Hong; Feng, Hong-Zhen; Ni, Pei

2006-08-01

The Lower Cambrian black shale sequence of the Niutitang Formation in the Yangtze Platform, South China, hosts an extreme metal-enriched sulfide ore bed that shows >10,000 times enrichment in Mo, Ni, Se, Re, Os, As, Hg, and Sb and >1,000 times enrichment in Ag, Au, Pt, and Pd, when compared to average upper continental crust. We report in this paper trace- and rare-earth-element concentrations and Pb-Pb isotope dating for the Ni-Mo-PGE-Au sulfide ores and their host black shales. Both the sulfide ores and their host black shales show similar trace-element distribution patterns with pronounced depletion in Th, Nb, Hf, Zr, and Ti, and extreme enrichment in U, Ni, Mo, and V compared to average upper crust. The high-field-strength elements, such as Zr, Hf, Nb, Ta, Sc, Th, rare-earth elements, Rb, and Ga, show significant inter-element correlations and may have been derived mainly from terrigenous sources. The redox sensitive elements, such as V, Ni, Mo, U, and Mn; base metals, such as Cu, Zn, and Pb; and Sr and Ba may have been derived from mixing of seawater and venting hydrothermal sources. The chondrite-normalized REE patterns, positive Eu and Y anomalies, and high Y/Ho ratios for the Ni-Mo-PGE-Au sulfide ores are also suggestive for their submarine hydrothermal-exhalative origin. A stepwise acid-leaching Pb-Pb isotope analytical technique has been employed for the Niutitang black shales and the Ni-Mo-PGE-Au sulfide ores, and two Pb-Pb isochron ages have been obtained for the black shales (531±24 Ma) and for the Ni-Mo-PGE-Au sulfide ores (521±54 Ma), respectively, which are identical and overlap within uncertainty, and are in good agreement with previously obtained ages for presumed age-equivalent strata.

Nutrient and trace-element enrichment of Coeur d'Alene Lake, Idaho

USGS Publications Warehouse

Woods, P.F.; Beckwith, M.A.

1996-01-01

The limnological characteristics and geochemistry of lakebed sediments in Coeur d'Alene Lake, a 129-square-kilometer, natural lake in northern Idaho, were assessed during 1991-92 because of the possible interaction of nutrient enrichment with the highly enriched trace-element concentrations stored in the lakebed. The lake was classified as oligotrophic during 1991-92 on the basis of annual geometric mean concentrations, in micrograms per liter, of total phosphorus (4.1), total nitrogen (247), and chlorophyll-a (0.54). Despite its oligotrophy, the lake developed a substantial hypolimnetic dissolved-oxygen deficit in both years during the later stage of thermal stratification. The lake's current trophic state of oligotrophic differs from the mesotrophic ranking it received in 1975 during the National Eutrophication Survey. The shift in trophic state was consistent with nutrient-load reductions that have occurred within the lake's 9,690-square-kilometer drainage basin since the early 1970's. Approximately 85 percent of the lakebed's surface area was highly enriched in antimony, arsenic, cadmium, lead, mercury, silver, and zinc. Mean total concentrations, in milligrams per kilogram, for cadmium, lead, and zinc in the enriched lakebed sediments were, respectively, 62, 1,900, and 3,600. In contrast, the concentrations of cadmium, lead, and zinc in unenriched lakebed sediments in the lake's southern end were, respec- tively, 2.8, 24, and 110 milligrams per kilogram. The vast majority of the trace elements in the surficial and subsurface sediments were associated with ferric oxides, not sulfides as previously postulated. Under reducing conditions, such as within as anoxic hypolimnon, the ferric oxide- associated trace elements would be readily soluble and available for release into the overlying water column. (USGS)

Trace element contents in fine particulate matter (PM2.5) in urban school microenvironments near a contaminated beach with mine tailings, Chañaral, Chile.

PubMed

Mesías Monsalve, Stephanie; Martínez, Leonardo; Yohannessen Vásquez, Karla; Alvarado Orellana, Sergio; Klarián Vergara, José; Martín Mateo, Miguel; Costilla Salazar, Rogelio; Fuentes Alburquenque, Mauricio; Cáceres Lillo, Dante D

2018-06-01

Air quality in schools is an important public health issue because children spend a considerable part of their daily life in classrooms. Particulate size and chemical composition has been associated with negative health effects. We studied levels of trace element concentrations in fine particulate matter (PM 2.5 ) in indoor versus outdoor school settings from six schools in Chañaral, a coastal city with a beach severely polluted with mine tailings. Concentrations of trace elements were measured on two consecutive days during the summer and winter of 2012 and 2013 and determined using X-ray fluorescence. Source apportionment and element enrichment were measured using principal components analysis and enrichment factors. Trace elements were higher in indoor school spaces, especially in classrooms compared with outdoor environments. The most abundant elements were Na, Cl, S, Ca, Fe, K, Mn, Ti, and Si, associated with earth's crust. Conversely, an extremely high enrichment factor was determined for Cu, Zn, Ni and Cr; heavy metals associated with systemic and carcinogenic risk effects, whose probably origin sources are industrial and mining activities. These results suggest that the main source of trace elements in PM 2.5 from these school microenvironments is a mixture of dust contaminated with mine tailings and marine aerosols. Policymakers should prioritize environmental management changes to minimize further environmental damage and its direct impact on the health of children exposed.

Vegetative Incompatibility and the Mating-Type Locus in the Cellular Slime Mold DICTYOSTELIUM DISCOIDEUM

PubMed Central

Robson, Gillian E.; Williams, Keith L.

1979-01-01

The genetic basis of vegetative incompatibility in the cellular slime mold, Dictyostelium discoideum, is elucidated. Vegetatively compatible haploid strains from parasexual diploids at a frequency of between 10-6 and 10-5, whereas "escaped" diploids are formed between vegetatively incompatible strains at a frequency of ∼10-8. There is probably only a single vegetative incompatibility site, which appears to be located at, or closely linked to, the mating-type locus. The nature of the vegetative incompatibility is deduced from parasexual diploid formation between wild isolates and tester strains of each mating type, examination of the frequency of formation of "escaped" diploids formed between vegetatively incompatible strains, and examination of the mating type and vegetative incompatibility of haploid segregants obtained from "escaped" diploids. PMID:17248984

Development of continental lithospheric mantle as reflected in the chemistry of the Mesozoic Appalachian Tholeiites, U.S.A.

NASA Astrophysics Data System (ADS)

Pegram, William J.

1990-03-01

Geochemical analyses of dikes, sills, and volcanic rocks of the Mesozoic Appalachian Tholeiite (MAT) Province of the easternmost United States provide evidence that continental tholeiites are derived from continental lithospheric mantle sources that are genetically and geochronologically related to the overlying continental crust. Nineteen olivine tholeiites and sixteen quartz tholeiites from the length of this province, associated in space and time with the last opening of the Atlantic, display significant isotopic heterogeneity: initial ɛ Nd = +3.8 to -5.7; initial 87Sr/ 86Sr= 0.7044-0.7072; 206Pb/ 204Pb= 17.49-19.14; 207Pb/ 204Pb= 15.55-15.65; 208Pb/ 204Pb= 37.24-39.11. In Pb sbnd Pb space, the MAT define a linear array displaced above the field for MORB and thus resemble oceanic basalts with DUPAL Pb isotopic traits. A regression of this array yields a secondary Pb sbnd Pb isochron age of ≈ 1000 Ma (μ 1 = 8.26), similar to Sm/Nd isochrons from the southern half of the province and to the radiometric age of the Grenville crust underlying easternmost North America. The MAT exhibit significant trace element ratio heterogeneity (e.g., Sm/Nd= 0.226-0.327) and have trace element traits similar to convergent margin magmas [e.g., depletions of Nb and Ti relative to the rare earth elements on normalized trace element incompatibility diagrams, Ba/Nb ratios (19-75) that are significantly greater than those of MORB, and low TiO 2 (0.39-0.69%)]. Geochemical and geological considerations very strongly suggest that the MAT were not significantly contaminated during ascent through the continental crust. Further, isotope and trace element variations are not consistent with the involvement of contemporaneous MORB or OIB components. Rather, the materials that control the MAT incompatible element chemistry were derived from subcontinental lithospheric mantle. Thus: (1) the MAT/arc magma trace element similarities; (2) the Pb sbnd Pb and Sm/Nd isochron ages; and (3) the need for a method of introducing an ancient (> 2-3 Ga) Pb component into subcontinental mantle that cannot be much older than 1 Ga leads to a model whereby the MAT were generated by the melting of sediment-contaminated arc mantle that was incorporated into the continental lithosphere during arc activity preceding the Grenville Orogeny (≈ 1000 Ma).

Implications for future activity of Grímsvötn volcano, Iceland, from compositional time series of historical tephra

NASA Astrophysics Data System (ADS)

Carpentier, Marion; Sigmarsson, Olgeir; Larsen, Gudrun

2014-05-01

The nature of future eruptions of active volcanoes is hard to predict. Improved understanding of the past volcanic activity is probably the best way to infer future eruptive scenarios. The most active volcano in Iceland, Grímsvötn, last erupted in 2011 with consequences for habitants living close to the volcano and aviation in the North-Atlantic. In an effort to better understand the magmatic system of the volcano, we have investigated the compositions of 23 selected tephra layers representing the last 8 centuries of volcanic activity at Grímsvötn. The tephra was collected in the ablation area of outlet glaciers from Vatnajökull ice cap. The ice-conserved tephra are less prone to alteration than those exposed in soil sections. Major element analyses are indistinguishable and of quartz-normative tholeiite composition, and Sr and Nd isotope ratios are constant. In contrast, both trace element concentrations (Th range from 0.875 ppm to 1.37 ppm and Ni from 28.5 ppm to 56.6 ppm) in the basalts and Pb isotopes show small but significant variations. The high-precision analyses of Pb isotope ratios allow the identification of tephra samples (3 in total) with more radiogenic ratios than the bulk of the samples. The tephra of constant isotope ratios show linear increase in incompatible element concentrations with time. The rate of increasing concentrations permits exploring possible future scenarios assuming that the magmatic system beneath the volcano follows the established historical evolution. Assuming similar future behaviour of the magma system beneath Grímsvötn volcano, the linear increase in e.g. Th concentration suggests that the volcano is likely to principally produce basalts for the next 500-1000 years. Evolution of water concentration will most likely follow those of incompatible elements with consequent increases in explosiveness of future Grímsvötn eruptions.

A combined basalt and peridotite perspective on 14 million years of melt generation at the Atlantis Bank segment of the Southwest Indian Ridge: Evidence for temporal changes in mantle dynamics?

USGS Publications Warehouse

Coogan, L.A.; Thompson, G.M.; MacLeod, C.J.; Dick, H.J.B.; Edwards, S.J.; Hosford, Scheirer A.; Barry, T.L.

2004-01-01

Little is known about temporal variations in melt generation and extraction at midocean ridges largely due to the paucity of sampling along flow lines. Here we present new whole-rock major and trace element data, and mineral and glass major element data, for 71 basaltic samples (lavas and dykes) and 23 peridotites from the same ridge segment (the Atlantis Bank segment of the Southwest Indian Ridge). These samples span an age range of almost 14 My and, in combination with the large amount of published data from this area, allow temporal variations in melting processes to be investigated. Basalts show systematic changes in incompatible trace element ratios with the older samples (from ???8-14 Ma) having more depleted incompatible trace element ratios than the younger ones. There is, however, no corresponding change in peridotite compositions. Peridotites come from the top of the melting column, where the extent of melting is highest, suggesting that the maximum degree of melting did not change over this interval of time. New and published Nd isotopic ratios of basalts, dykes and gabbros from this segment suggest that the average source composition has been approximately constant over this time interval. These data are most readily explained by a model in which the average source composition and temperature have not changed over the last 14 My, but the dynamics of mantle flow (active-to-passive) or melt extraction (less-to-more efficient extraction from the 'wings' of the melting column) has changed significantly. This hypothesised change in mantle dynamics occurs at roughly the same time as a change from a period of detachment faulting to 'normal' crustal accretion. We speculate that active mantle flow may impart sufficient shear stress on the base of the lithosphere to rotate the regional stress field and promote the formation of low angle normal faults. ?? 2004 Elsevier B.V. All rights reserved.

Combining and comparing neutrinoless double beta decay experiments using different nuclei

NASA Astrophysics Data System (ADS)

Bergström, Johannes

2013-02-01

We perform a global fit of the most relevant neutrinoless double beta decay experiments within the standard model with massive Majorana neutrinos. Using Bayesian inference makes it possible to take into account the theoretical uncertainties on the nuclear matrix elements in a fully consistent way. First, we analyze the data used to claim the observation of neutrinoless double beta decay in 76Ge, and find strong evidence (according to Jeffrey's scale) for a peak in the spectrum and moderate evidence for that the peak is actually close to the energy expected for the neutrinoless decay. We also find a significantly larger statistical error than the original analysis, which we include in the comparison with other data. Then, we statistically test the consistency between this claim with that of recent measurements using 136Xe. We find that the two data sets are about 40 to 80 times more probable under the assumption that they are inconsistent, depending on the nuclear matrix element uncertainties and the prior on the smallest neutrino mass. Hence, there is moderate to strong evidence of incompatibility, and for equal prior probabilities the posterior probability of compatibility is between 1.3% and 2.5%. If one, despite such evidence for incompatibility, combines the two data sets, we find that the total evidence of neutrinoless double beta decay is negligible. If one ignores the claim, there is weak evidence against the existence of the decay. We also perform approximate frequentist tests of compatibility for fixed ratios of the nuclear matrix elements, as well as of the no signal hypothesis. Generalization to other sets of experiments as well as other mechanisms mediating the decay is possible.

Geochemical fingerprinting of ∼2.5 Ga forearc-arc-backarc related magmatic suites in the Bastar Craton, central India

NASA Astrophysics Data System (ADS)

Asthana, Deepanker; Kumar, Sirish; Vind, Aditya Kumar; Zehra, Fatima; Kumar, Harshavardhan; Pophare, Anil M.

2018-05-01

The Pitepani volcanic suite of the Dongargarh Supergroup, central India comprises of a calc-alkaline suite and a tholeiitic suite, respectively. The rare earth element (REE) patterns, mantle normalized plots and relict clinopyroxene chemistry of the Pitepani calc-alkaline suite are akin to high-Mg andesites (HMA) and reveal remarkable similarity to the Cenozoic Setouchi HMA from Japan. The Pitepani HMAs are geochemically correlated with similar rocks in the Kotri-Dongargarh mobile belt (KDMB) and in the mafic dykes of the Bastar Craton. The rationale behind lithogeochemical correlations are that sanukitic HMAs represent fore-arc volcanism over a very limited period of time, under abnormally high temperature conditions and are excellent regional and tectonic time markers. Furthermore, the tholeiitic suites that are temporally and spatially associated with the HMAs in the KDMB and in the mafic dykes of the Bastar Craton are classified into: (a) a continental back-arc suite that are depleted in incompatible elements, and (b) a continental arc suite that are more depleted in incompatible elements, respectively. The HMA suite, the continental back-arc and continental arc suites are lithogeochemically correlated in the KDMB and in the mafic dykes of the Bastar Craton. The three geochemically distinct Neoarchaean magmatic suites are temporally and spatially related to each other and to an active continental margin. The identification of three active continental margin magmatic suites for the first time, provides a robust conceptual framework to unravel the Neoarchaean geodynamic evolution of the Bastar Craton. We propose an active continental margin along the Neoarchaen KDMB with eastward subduction coupled with slab roll back or preferably, ridge-subduction along the Central Indian Tectonic Zone (CITZ) to account for the three distinct magmatic suites and the Neoarchean geodynamic evolution of the Bastar Craton.

A Simulated Geochemical Rover Mission to the Taurus-Littrow Valley of the Moon

NASA Technical Reports Server (NTRS)

Korotev, Randy L.; Haskin, Larry A.; Jolliff, Bradley L.

1995-01-01

We test the effectiveness of using an alpha backscatter, alpha-proton, X ray spectrometer on a remotely operated rover to analyze soils and provide geologically useful information about the Moon during a simulated mission to a hypothetical site resembling the Apollo 17 landing site. On the mission, 100 soil samples are "analyzed" for major elements at moderate analytical precision (e.g., typical relative sample standard deviation from counting statistics: Si[11%], Al[18%], Fe[6%], Mg[20%], Ca[5%]). Simulated compositions of soils are generated by combining compositions of components representing the major lithologies occurring at the site in known proportions. Simulated analyses are generated by degrading the simulated compositions according to the expected analytical precision of the analyzer. Compositions obtained from the simulated analyses are modeled by least squares mass balance as mixtures of the components, and the relative proportions of those components as predicted by the model are compared with the actual proportions used to generate the simulated composition. Boundary conditions of the modeling exercise are that all important lithologic components of the regolith are known and are represented by model components, and that the compositions of these components are well known. The effect of having the capability of determining one incompatible element at moderate precision (25%) is compared with the effect of the lack of this capability. We discuss likely limitations and ambiguities that would be encountered, but conclude that much of our knowledge about the Apollo 17 site (based on the return samples) regarding the distribution and relative abundances of lithologies in the regolith could be obtained. This success requires, however, that at least one incompatible element be determined.

Positive anomalous concentrations of Pb in some gabbroic rocks of Afikpo basin southeastern Nigeria.

PubMed

Onwualu-John, J N

2016-08-01

Gabbroic rocks have intruded the sedimentary sequence at Ameta in Afikpo basin southeastern Nigeria. Petrographic and geochemical features of the rocks were studied in order to evaluate their genetic and geotectonic history. The petrographic results show that the rocks contain plagioclase, olivine, pyroxene, biotite, iron oxide, and traces of quartz in three samples. Major element characteristics show that the rocks are subalkaline. In addition, the rocks have geochemical characteristics similar to basaltic andesites. The trace elements results show inconsistent concentrations of high field strength elements (Zr, Nb, Th, Ta), moderate enrichment of large-ion lithophile elements (Rb, Sr, Ba) and low concentrations of Ni and Cr. Rare earth element results show that the rocks are characterized by enrichment of light rare earth elements, middle rare earth elements enrichment, and depletion of heavy rare earth elements with slight positive europium anomalies. Zinc concentrations are within the normal range in basaltic rocks. There are extremely high concentrations of Pb in three of the rock samples. The high Pb concentrations in some of these rocks could be as a result of last episodes of magmatic crystallization. The rocks intruded the Asu River Group; organic components in the sedimentary sequence probably contain Pb which has been assimilated into the magma at the evolutionary stage of the magma. Weathering of some rocks that contain galena could lead to an increase in the concentration of lead in the gabbroic rocks, especially when the migration and crystallization of magma take place in an aqueous environment. Nevertheless, high concentration of lead is hazardous to health and environment.

Local finite element enrichment strategies for 2D contact computations and a corresponding post-processing scheme

NASA Astrophysics Data System (ADS)

Sauer, Roger A.

2013-08-01

Recently an enriched contact finite element formulation has been developed that substantially increases the accuracy of contact computations while keeping the additional numerical effort at a minimum reported by Sauer (Int J Numer Meth Eng, 87: 593-616, 2011). Two enrich-ment strategies were proposed, one based on local p-refinement using Lagrange interpolation and one based on Hermite interpolation that produces C 1-smoothness on the contact surface. Both classes, which were initially considered for the frictionless Signorini problem, are extended here to friction and contact between deformable bodies. For this, a symmetric contact formulation is used that allows the unbiased treatment of both contact partners. This paper also proposes a post-processing scheme for contact quantities like the contact pressure. The scheme, which provides a more accurate representation than the raw data, is based on an averaging procedure that is inspired by mortar formulations. The properties of the enrichment strategies and the corresponding post-processing scheme are illustrated by several numerical examples considering sliding and peeling contact in the presence of large deformations.

Outcomes after ABO-incompatible heart transplantation in adults: A registry study.

PubMed

Bergenfeldt, Henrik; Andersson, Bodil; Bućin, Dragan; Stehlik, Josef; Edwards, Leah; Rådegran, Göran; Nilsson, Johan

2015-07-01

In the past, ABO incompatibility was considered an absolute contraindication to heart transplantation (HT) in adults. Advances in ABO-incompatible HT in pediatric patients and ABO-incompatible abdominal transplantation in adult patients have led to clinical exploration of intentional ABO-incompatible HT in adults. However, it is not well known how outcomes in ABO-incompatible adult heart transplant recipients compare with outcomes in ABO-compatible recipients. We analyzed International Society for Heart and Lung Transplantation transplant registry data from heart donors and recipients ≥18 years old at the time of transplant for HT performed between 1988 and 2011. We compared baseline characteristics and post-transplant outcomes in ABO-incompatible and ABO-compatible HT. Death or retransplantation was the composite primary end-point. Among 76,663 adult patients undergoing HT between 1988 and June 30, 2011, 94 ABO-incompatible heart transplants were performed. The incidence of death or retransplantation in the ABO-incompatible group was higher than in the ABO-compatible group: 21% vs 9% at 30 days (hazard ratio = 2.38, p < 0.001) and 36% vs 19% at 1 year after transplant. However, ABO-incompatible grafts surviving past the first year after transplant had a similar incidence of failure compared with the ABO-compatible group. After 2005, the rate ABO-incompatible HT in adults increased, likely as a result of planned, intentional (rather than accidental) ABO-incompatible HT. In this group of patients, short-term and long-term incidence of death or retransplantation was similar to ABO-compatible recipients (p = 0.822): 7% at 30 days and 19% at 1 year after transplantation. We found no difference in incidence of death or retransplantation between ABO-compatible and ABO-incompatible HT in patients who underwent transplantation after 2005. Copyright © 2015 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

Origin of Tungsten Excess in Komatiites

NASA Astrophysics Data System (ADS)

Becker, H.; Brandon, A. D.; Walker, R. J.

2004-12-01

The limited database available for W abundances in komatiites (n=7, Newsom et al., 1996) suggests that when melting and fractional crystallization effects are filtered out, these komatiites have about 10 times higher W, compared to other mantle-derived mafic-ultramafic magmas (MORB, OIB). The excess of W in the komatiites relative to lithophile highly incompatible elements becomes obvious when compared with the low concentrations of the light REE Ce and Nd (about 1-2 ug/g in many komatiites, compared to > 10 ug/g in most MORB and OIB). In order to increase the komatiite W database, komatiite samples from Phanerozoic (Gorgona Island) and Archean terraines (Boston Creek/Canada, Belingwe/South Africa, 2.7 Ga) were dissolved and W was separated in order to obtain W concentrations by isotope dilution. Except for one sample from Gorgona Island with low W (23 ng/g), samples from all three locales show high W (516 to 2643 ng/g), with most samples containing near 700 ng/g W. Three Hawaiian picrites (H23, LO-02-04, MK-1-6) were also analyzed for comparative purposes and contain 75, 163 and 418 ng/g W, respectively. The W concentrations in the Hawaiian picrites are comparable or lower than W concentrations in Hawaiian tholeiites (Newsom et al., 1996). Mass balance considerations suggest that it is unlikely that the W excess in komatiites reflects W contributions to the mantle sources of komatiites from the outer core. The W enrichment could result from shallow-level alteration processes if primary W abundances of komatiites were low and W was added via fluids, containing W and other fluid-mobile elements derived from crustal rocks. Because most W in such samples would be of crustal origin, small contributions from the outer core may be difficult to detect using 182W systematics (Schersten et al., 2003).

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.

Mantle xenoliths hosted in alkali basalts in subduction environment: the example of the SE Alps (Italy)

NASA Astrophysics Data System (ADS)

Gasperini, D.; Maffei, K.; Bosch, D.; Braga, R.; Macera, P.; Morten, L.

2003-04-01

We present petrographic, geochemical, and isotopic (Sr, Nd, and Pb) data of a representative suite of spl-peridotite xenoliths (mg# >88) hosted in alkali basalts from numerous outcrops in the Tertiary Veneto Volcanic Province (VVP; SE Alps, Italy), compared to various world-wide mafic inclusions (French Massif, Australia, China, Philippines, Russia, Kerguelen). The VVP spl-harzburgites and -lherzolites carry textures ranging from protogranular, porphyroclastic, granuloblastic to pyrometamorfic. These samples are characterized by a continuous depletion trend from the cpx-rich lherzolites to harzburgites, with CaO, Al_2O_3, TiO_2, and Na_2O contents decreasing with mg# increasing (Morten, 1987; Beccaluva et al., 2001). Then, the VVP xenoliths spinels show a strong Cr/(Cr+Al) ratio increase at a slight Mg/(Mg+Fe2+) ratio decrease, thus reflecting a variably depleted mantle source. The VVP xenoliths display a large range of enrichment in LREE, K, Rb, Sr and P, suggesting post depletion metasomatic episodes (Morten et al., 2002). Whereas most of the VVP xenoliths' multi-element spectra, incompatible element and isotope ratios are similar to the VVP host basalts, thus with a strong HIMU signature (Macera et al. submitted), some depleted samples show geochemical features typical of crust derived material. These characteristics cannot be related to significant interaction with the local lower continental crust, as represented by several analyzed gabbroic xenoliths. Nevertheless negative Nb and Ta anomalies in analogous peridotitic samples have been previously ascribed to metasomatism inferred by plume rising material in the upper mantle (Bedini et al., 1997). Comparing the VVP peridotites with several mafic xenoliths from various geodynamical environments, we suggest that this crust affinity could be alternatively explained by the presence of a not perfectly homogenized upper crustal component in the source region, probably induced by subduction related episode(s). In this contest, the isotopic composition of the VVP mafic xenoliths is a crucial tool to understand the geochemical history of the Alpine subcontinental mantle.

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.

The Martian Soil as a Geochemical Sink for Hydrothermally Altered Crustal Rocks and Mobile Elements: Implications of Early MER Results

NASA Technical Reports Server (NTRS)

Newsom, H. E.; Nelson, M. J.; Shearer, C. K.; Draper, D. S.

2005-01-01

Hydrothermal and aqueous alteration can explain some of the exciting results from the MER team s analyses of the martian soil, including the major elements, mobile elements, and the nickel enrichment. Published results from the five lander missions lead to the following conclusions: 1) The soil appears to be globally mixed and basaltic with only small local variations in chemistry. Relative to martian basaltic meteorites and Gusev rocks the soils are depleted in the fluid-mobile element calcium, but only slightly enriched to somewhat depleted in iron oxide. 2) The presence of olivine in the soils based on M ssbauer data argues that the soil is only partly weathered and is more akin to a lunar regolith than a terrestrial soil. 3) The presence of bromine along with sulfur and chlorine in the soils is consistent with addition of a mobile element component to the soil.

Neutron source, linear-accelerator fuel enricher and regenerator and associated methods

DOEpatents

Steinberg, Meyer; Powell, James R.; Takahashi, Hiroshi; Grand, Pierre; Kouts, Herbert

1982-01-01

A device for producing fissile material inside of fabricated nuclear elements so that they can be used to produce power in nuclear power reactors. Fuel elements, for example, of a LWR are placed in pressure tubes in a vessel surrounding a liquid lead-bismuth flowing columnar target. A linear-accelerator proton beam enters the side of the vessel and impinges on the dispersed liquid lead-bismuth columns and produces neutrons which radiate through the surrounding pressure tube assembly or blanket containing the nuclear fuel elements. These neutrons are absorbed by the natural fertile uranium-238 elements and are transformed to fissile plutonium-239. The fertile fuel is thus enriched in fissile material to a concentration whereby they can be used in power reactors. After use in the power reactors, dispensed depleted fuel elements can be reinserted into the pressure tubes surrounding the target and the nuclear fuel regenerated for further burning in the power reactor.

Volatile elements in and on lunar volcanic glasses: What do they tell us about lunar genesis?

NASA Technical Reports Server (NTRS)

Koeberl, C.

1984-01-01

There are good reasons to believe that lunar volcanic glasses originated from a deep interior source. The presence of a thin layer of surface correlated elements on these glasses may indicate that the Moon has some reservoirs that are enriched in volatiles. Since the glasses themselves do not show similar enrichment, the source should be of limited extent. Three scenarios are advanced for the origin of these elements. The mechanism for lunar volcanism differs from the mechanism for volcanism on Earth since the former produces bubbling and the latter explosive fountaining. From the condensation behavior of the volatile compounds, which leads to heterogeneous condensation, it is concluded that comparing element ratios of surface correlated elements gives little sense. It seems as if the volatile reservoirs are of rather limited extent and that they do not enlarge the volatile content of the bulk Moon significantly.

Hf-Nd Isotopic Correlation in the Deccan Flood Basalt Province

NASA Astrophysics Data System (ADS)

Saha, A.; Basu, A. R.; Barling, J.; Anbar, A. D.; Hooper, P. R.

2001-12-01

Hafnium isotopes along with other isotopic and geochemical characteristics, including incompatible trace elements, of several of the lower formations of the Deccan Flood Basalt Province were analyzed to characterize petrogenesis of different tholeiitic lava suites, especially with respect to potential mantle and crustal sources. The rare earth elements of the different formations (from top to bottom- Mahabaleshwar, Ambenali, Bushe, Khandala and Neral) all show an LREE-enriched signature, concentrations varying between 30 to 60 times chondrite for La. (La/Lu)n values range from 4.1 to above 8 with the exception of Ambenali, which has a less LREE-enriched signature with (La/Lu)n values ranging between 3.6 to 5.3. Hafnium isotopic data of the lower formations of the Deccan show initial \\epsilonHf(T) values covering a range from -3 to -28. 176Lu/177Hf varies between 0.20 to 0.70. f(Lu/Hf) varies within a narrow range, between -0.90 to -0.97 while f(Sm/Nd) ranges from -0.84 to -0.86. Bushe gives the lowest range of \\epsilonHf(T) from -21 to -28 with the corresponding \\epsilonNd(T) varying between -4.0 and -16.9, while Khandala for almost the same range of neodymium isotopic values has \\epsilonHf(T) between -11 and -15. The \\epsilonHf(T) values of Neral is in between those of Khandala and Bushe, around -19. Ambenali, has the narrowest range with \\epsilonHf(T) of -3 and \\epsilonNd(T) between 3 and 5. The Ambenali suite reflects the least contaminated of the Deccan suite of lavas as analyzed here and previously confirmed by other isotopic studies. In Hf-Nd isotope correlation plot, the lower Deccan formations of Neral, Khandala and Bushe define individual subparallel arrays that are shallower than the oceanic basalt array and the overall terrestrial array, including the crustal array, although the bulk of the lower formation data fall within the crustal array of Vervoort et al (1999). From these subparallel Hf-Nd arrays, it is evident that the other end-members contributing to the Ambenali-type source magmas are distinctly different for each of these lava suites, and can be characterized by their \\epsilonHf(T) values as mentioned above. Although these end-members are discernible in \\epsilonNd vs \\epsilonSr plot (e.g., Peng et al, 1994) of previous studies, our new Hf-isotopic data provide clear evidence of major contributions from the ancient Indian continental crustal reservoirs in the petrogenesis of the lower lava formations of the Deccan Flood Basalt Province.

De novo mutations in regulatory elements in neurodevelopmental disorders

PubMed Central

Short, Patrick J.; McRae, Jeremy F.; Gallone, Giuseppe; Sifrim, Alejandro; Won, Hyejung; Geschwind, Daniel H.; Wright, Caroline F.; Firth, Helen V; FitzPatrick, David R.; Barrett, Jeffrey C.; Hurles, Matthew E.

2018-01-01

We previously estimated that 42% of patients with severe developmental disorders carry pathogenic de novo mutations in coding sequences. The role of de novo mutations in regulatory elements affecting genes associated with developmental disorders, or other genes, has been essentially unexplored. We identified de novo mutations in three classes of putative regulatory elements in almost 8,000 patients with developmental disorders. Here we show that de novo mutations in highly evolutionarily conserved fetal brain-active elements are significantly and specifically enriched in neurodevelopmental disorders. We identified a significant twofold enrichment of recurrently mutated elements. We estimate that, genome-wide, 1-3% of patients without a diagnostic coding variant carry pathogenic de novo mutations in fetal brain-active regulatory elements and that only 0.15% of all possible mutations within highly conserved fetal brain-active elements cause neurodevelopmental disorders with a dominant mechanism. Our findings represent a robust estimate of the contribution of de novo mutations in regulatory elements to this genetically heterogeneous set of disorders, and emphasize the importance of combining functional and evolutionary evidence to identify regulatory causes of genetic disorders. PMID:29562236

Post-Hercynian subvolcanic magmatism in the Serre Massif (Central-Southern Calabria, Italy)

NASA Astrophysics Data System (ADS)

Romano, V.; Cirrincione, R.; Fiannacca, P.; Mazzoleni, P.; Tranchina, A.

2009-04-01

In the Serre Massif (Central-Southern Calabria, Italy) dykes and subvolcanic bodies intrude diffusively both Hercynian metamorphic rocks and late-Hercynian granitoids. They range in composition from basaltic andesites to dacite-rhyodacites and can be ascribed to the extensive magmatic activity that affects the entire Hercynian orogenic belt in late Paleozoic - early Mesozoic time. The geodinamic framework of the magmatic activity is still matter of debate, nevertheless most authors agree in correlating magmatism both to the late-orogenic collapse of the Hercynian belt and to the lithosphere thinning responsible for the subsequent continental rifting. In this work, we propose a petrogenetic model for acidic to basic hypabissal bodies from southern Calabria in order to define the nature of sources, discriminate magmatic processes and supply a contribution in the geodynamic reconstruction of the Late Palaeozoic in the Calabria-Peloritani Orogen. In relation to their geochemical affinity, studied dykes have been divided in two groups: a medium- to high-K calc-alkaline and a tholeiitic one. Dykes belonging to the former group, andesitic and dacitic-rhyodacitic in composition, show typical features of subduction-related magmatism, such as LILE and LREE enrichments, depletions in HFSE, peaks in Rb, Th and Ce, accentuated troughs in Ba, Nb-Ta, P and Ti (White and Dupré, 1986; McCulloch and Gamble, 1991), contrasting with the late Hercynian collisional context. On the other side, features typical of intra-plate magmatic activity, such as a moderate enrichment in Ta, Nb, Ce, P, Zr, Hf and Sm relative to MORB composition are also present in studied rocks (Shimizu & Arculus, 1975; Pearce, 1982). REE-patterns are strongly to weakly fractionated for the andesitic rocks (Lan/Ybn = 10.03-13.98) and the dacitic-rhyodacitic ones (Lan/Ybn = 6.00 to 2.82), respectively. The latter rocks exhibit a very slight negative Eu anomaly, whereas no Eu anomaly is recognizable in the andesite patterns. For the andesite rocks an origin by partial melting of an enriched lithospheric mantle source in a post-collisional context is proposed. For dacitic-rhyodacitic dykes a strong involvement of crustal material is suggested by geochemical features such as Nb-Ta trough, Th enrichment, low Nb/La rate (0.37 avg value) and high Th/La rate (0.68 avg value) (Taylor & McLennan, 1985). Tholeiitic dykes include basaltic andesites with geochemical characteristics (REE and incompatible elements) very similar to those of continental tholeiites. Nb and Ti anomalies, less marked of those observed in calc-alkaline dykes, also occur in the tholeiitic ones, as well as the enrichment in LIL elements. Besides, with respect the calc-alkaline ones, tholeiitic types are slightly more HFSE-enriched. REE patterns are sub-parallel and slightly fractionated (Lan/Ybn = 2.62 and 2.65), Eu negative anomaly is strongly pronounced. These geochemical evidences are explained invoking a derivation from an enriched mantle source, possibly in connection with early stages of continental rifting processes. Crustal contamination or magma mixing processes probably occurred during magma ascent, as suggested by petrographic evidences ("quartz ocelli" and xenocrysts of plagioclase). Indeed, even by comparing N-MORB - normalized patterns of tholeiitic dykes with E-MORB (Sun, 1980) and upper continental crust (Taylor and McLennan, 1981) compositions, a derivation from an E-MORB source type and interaction with continental crust both appear as processes strongly involved in the genesis of the studied rocks. REFERENCES: • McCulloch M.T. and Gamble J.A. (1991) - Earth Plan. Sci. Lett., 102, 358-374. • Pearce J. A. (1982) - Ed. Thorpe R. S., 525-548. John Wiley & Sons, New York. • Shimizu N. and Arculus R. J. (1975) - Contrib. Mineral. Petrol., 50, 231-240. • Sun S. S. (1980) - Phil. Trans. R. Soc., A297, 409-445. • Taylor S. R. and McLennan S. M. (1981) - Phil. Trans. R. Soc., A301, 381-399. • Taylor S. R. and McLennan S. M. (1985) - Oxford: Blackwell Scientific, 312 pp. • White W.M. and Dupré B. (1986) - J. Geophys. Res., 91, 5927-5941.

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.

Effects of Enrichment Presentation and Other Factors on Behavioral Welfare of Pantropical Spotted Dolphin (Stenella attenuata).

PubMed

Perez, Barbara C; Mehrkam, Lindsay R; Foltz, Amanda R; Dorey, Nicole R

2018-01-01

Environmental enrichment is a crucial element of promoting welfare for animals in captivity. However, enrichment programs are not always formally evaluated for their efficacy. Furthermore, there is little empirical evidence of enrichment evaluation for species of small cetaceans in zoological settings. A wide range of variables may potentially influence enrichment efficacy and how it in turn affects behavior. The purpose of this study was to determine the most preferred environmental enrichment, and method of presentation, for a species that has not been well studied in captivity, the pantropical spotted dolphin (Stenella attenuata). In order to determine which enrichment items and method of presentation were most effective at eliciting enrichment interaction, we systematically examined how several variables of enrichment influenced enrichment interaction. The results suggested that presenting enrichment after training sessions influenced interaction with the enrichment. The results also indicated preference for enrichment type and a specific enrichment device. Finally, factors that influenced interaction were also found to influence aberrant behavior. The results support the premise that enrichment be "redefined" for each species and each individual.

Sulfide in the core and the composition of the silicate Earth

NASA Astrophysics Data System (ADS)

Burton, K. W.

2015-12-01

The chemical composition of the Earth is traditionally explained in terms of evolution from a solar-like composition, similar to that found in primitive 'chondritic' meteorites. It now appears, however, that the silicate Earth is not 'chondritic', but depleted in incompatible elements, including refractory lithophile and heat-producing elements. Either Earth lost material during planet-building due to collisional erosion or else internal differentiation processes produced a hidden reservoir deep in the early Earth. Sulfide in the core may provide a reservoir capable of balancing the composition of the silicate Earth. Recent experimental work suggests that the core contains a significant proportion of sulfide, added during the final stages of accretion and new data suggests that at high pressures sulfide can incorporate a substantial amount of refractory lithophile and heat-producing elements [1]. Pioneering work using the short-lived 146Sm-142Nd system strongly suggests that Earth's silicate mantle is non-chondritic [e.g. 2]. The drawback of such radiogenic isotope systems is that it is not possible to distinguish the fractionation of Sm/Nd that occurs during silicate melting from that occurring during the segregation of a sulfide-melt to form the core. Neodymium stable isotopes have the potential to provide just such a tracer of sulfide segregation, because there is a significant contrast in bonding environment between sulfide and silicate, where heavy isotopes should be preferentially incorporated into high force-constant bonds involving REE3+ (i.e. the silicate mantle). Preliminary data indicate that mantle rocks do indeed possess heavier 146Nd/144Nd values than chondritic meteorites, consistent with the removal of light Nd into sulfide in the core, driving the residual mantle to heavy values. Overall, our isotope and elemental data indicate that the rare earths and other incompatible elements are substantially incorporated into sulfide. While Nd Stable isotope data for chondritic meteorites and mantle rocks, are consistent with the segregation of sulfide to the core. [1] Wohlers &Wood, Nature 520, 337 (2015) [2] Boyet & Carlson, Science 309, 576 (2005)

Along-strike variability of primitive magmas (major and volatile elements) inferred from olivine-hosted melt inclusions, southernmost Andean Southern Volcanic Zone, Chile

NASA Astrophysics Data System (ADS)

Weller, D. J.; Stern, C. R.

2018-01-01

Glass compositions of melt inclusions in olivine phenocrysts found in tephras derived from explosive eruptions of the four volcanoes along the volcanic front of the southernmost Andean Southern Volcanic Zone (SSVZ) are used to constrain primitive magma compositions and melt generation parameters. Primitive magmas from Hudson, Macá, and Melimoyu have similar compositions and are formed by low degrees (8-18%) of partial melting. Compared to these other three centers, primitive magmas from Mentolat have higher Al2O3 and lower MgO, TiO2 and other incompatible minor elements, and are generated by somewhat higher degrees (12-20%) of partial melting. The differences in the estimated primitive parental magma compositions between Mentolat and the other three volcanic centers are consistent with difference in the more evolved magmas erupted from these centers, Mentolat magmas having higher Al2O3 and lower MgO, TiO2 and other incompatible minor element contents, suggesting that these differences are controlled by melting processes in the mantle source region above the subducted oceanic plate. Parental magma S = 1430-594 and Cl = 777-125 (μg/g) contents of Hudson, Macá, and Melimoyu are similar to other volcanoes further north in the SVZ. However, Mentolat primitive magmas have notably higher concentrations of S = 2656-1227 and Cl = 1078-704 (μg/g). The observed along-arc changes in parental magma chemistry may be due to the close proximity below Mentolat of the subducted Guamblin Fracture Zone that could efficiently transport hydrous mineral phases, seawater, and sediment into the mantle, driving enhanced volatile fluxed melting beneath this center compared to the others. Table S2. Olivine-hosted melt inclusion compositions, host-olivine compositions, and the post-entrapment crystallization corrected melt inclusion compositions. Table S3. Olivine-hosted melt inclusion modeling information. Table S4. Major element compositions of the fractionation corrected melt inclusion in equilibrium with mantle olivine. Table S5. Melting parameters Fm and CoH2O. Table S6. Major element compositions of phenocrysts and glasses occurring with the olivine-hosted melt inclusions.

Elements of the corruption crime (element analysis of authority abuse and self-enrich and corporations in Indonesia)

NASA Astrophysics Data System (ADS)

Mandasari Saragih, Yasmirah; Medaline, Onny

2018-03-01

In effect the authority abuse very closely relates to the presence of invalidity (disability juridical) of a decision or government action/state officials. Sadjijono, by citing the opinion of M. Hadjon Phlipus suggests that defective judicial decision or government action/state officials generally involves three main elements, namely the element of authority, the element of the procedure and elements of substance, thus flawed judicial action state officials can be classified into three kinds, namely: disability authority, defective procedure and substance defects. The three of them are the essence of the onset authority abuse. Their acts that profitable and or self-enrich or another person or entity covering for the authority abuse or opportunity. These criteria have been expanded because there is a term for position and so on, including bribery, both among non-civil and public servants. Reciprocally with the given gifts and the promise of the new legislation, the criteria have been expanded.

Mineralogy and petrogenesis of lunar magnesian granulitic meteorite Northwest Africa 5744

NASA Astrophysics Data System (ADS)

Kent, Jeremy J.; Brandon, Alan D.; Joy, Katherine H.; Peslier, Anne H.; Lapen, Thomas J.; Irving, Anthony J.; Coleff, Daniel M.

2017-09-01

Lunar meteorite Northwest Africa (NWA) 5744 is a granulitic breccia with an anorthositic troctolite composition that may represent a distinct crustal lithology not previously described. This meteorite is the namesake and first-discovered stone of its pairing group. Bulk rock major element abundances show the greatest affinity to Mg-suite rocks, yet trace element abundances are more consistent with those of ferroan anorthosites. The relatively low abundances of incompatible trace elements (including K, P, Th, U, and rare earth elements) in NWA 5744 could indicate derivation from a highlands crustal lithology or mixture of lithologies that are distinct from the Procellarum KREEP terrane on the lunar nearside. Impact-related thermal and shock metamorphism of NWA 5744 was intense enough to recrystallize mafic minerals in the matrix, but not intense enough to chemically equilibrate the constituent minerals. Thus, we infer that NWA 5744 was likely metamorphosed near the lunar surface, either as a lithic component within an impact melt sheet or from impact-induced shock.

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.

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.

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.

The new model of chemical evolution of r-process elements based on the hierarchical galaxy formation. I. Ba and Eu

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

Komiya, Yutaka; Suda, Takuma; Yamada, Shimako

2014-03-10

We investigate the chemical enrichment of r-process elements in the early evolutionary stages of the Milky Way halo within the framework of hierarchical galaxy formation using a semi-analytic merger tree. In this paper, we focus on heavy r-process elements, Ba and Eu, of extremely metal-poor (EMP) stars and give constraints on their astronomical sites. Our models take into account changes of the surface abundances of EMP stars by the accretion of interstellar medium (ISM). We also consider metal-enrichment of intergalactic medium by galactic winds and the resultant pre-enrichment of proto-galaxies. The trend and scatter of the observed r-process abundances aremore » well reproduced by our hierarchical model with ∼10% of core-collapse supernovae in low-mass end (∼10 M {sub ☉}) as a dominant r-process source and the star formation efficiency of ∼10{sup –10} yr{sup –1}. For neutron star mergers as an r-process source, their coalescence timescale has to be ∼10{sup 7} yr, and the event rates ∼100 times larger than currently observed in the Galaxy. We find that the accretion of ISM is a dominant source of r-process elements for stars with [Ba/H] < –3.5. In this model, a majority of stars at [Fe/H] < –3 are formed without r-process elements, but their surfaces are polluted by the ISM accretion. The pre-enrichment affects ∼4% of proto-galaxies, and yet, is surpassed by the ISM accretion in the surface of EMP stars.« less

SNC meteorites and their implications for reservoirs of Martian volatiles

NASA Technical Reports Server (NTRS)

Jones, J. H.

1993-01-01

The SNC meteorites and the measurements of the Viking landers provide our only direct information about the abundance and isotopic composition of Martian volatiles. Indirect measurements include spectroscopic determinations of the D/H ratio of the Martian atmosphere. A personal view of volatile element reservoirs on Mars is presented, largely as inferred from the meteoritic evidence. This view is that the Martian mantle has had several opportunities for dehydration and is most likely dry, although not completely degassed. Consequently, the water contained in SNC meteorites was most likely incorporated during ascent through the crust. Thus, it is possible that water can be decoupled from other volatile/incompatible elements, making the SNC meteorites suspect as indicators of water inventories on Mars.

Finite cover method with mortar elements for elastoplasticity problems

NASA Astrophysics Data System (ADS)

Kurumatani, M.; Terada, K.

2005-06-01

Finite cover method (FCM) is extended to elastoplasticity problems. The FCM, which was originally developed under the name of manifold method, has recently been recognized as one of the generalized versions of finite element methods (FEM). Since the mesh for the FCM can be regular and squared regardless of the geometry of structures to be analyzed, structural analysts are released from a burdensome task of generating meshes conforming to physical boundaries. Numerical experiments are carried out to assess the performance of the FCM with such discretization in elastoplasticity problems. Particularly to achieve this accurately, the so-called mortar elements are introduced to impose displacement boundary conditions on the essential boundaries, and displacement compatibility conditions on material interfaces of two-phase materials or on joint surfaces between mutually incompatible meshes. The validity of the mortar approximation is also demonstrated in the elastic-plastic FCM.

Clustering in the stellar abundance space

NASA Astrophysics Data System (ADS)

Boesso, R.; Rocha-Pinto, H. J.

2018-03-01

We have studied the chemical enrichment history of the interstellar medium through an analysis of the n-dimensional stellar abundance space. This work is a non-parametric analysis of the stellar chemical abundance space. The main goal is to study the stars from their organization within this abundance space. Within this space, we seek to find clusters (in a statistical sense), that is, stars likely to share similar chemo-evolutionary history, using two methods: the hierarchical clustering and the principal component analysis. We analysed some selected abundance surveys available in the literature. For each sample, we labelled the group of stars according to its average abundance curve. In all samples, we identify the existence of a main enrichment pattern of the stars, which we call chemical enrichment flow. This flow is set by the structured and well-defined mean rate at which the abundances of the interstellar medium increase, resulting from the mixture of the material ejected from the stars and stellar mass-loss and interstellar medium gas. One of the main results of our analysis is the identification of subgroups of stars with peculiar chemistry. These stars are situated in regions outside of the enrichment flow in the abundance space. These peculiar stars show a mismatch in the enrichment rate of a few elements, such as Mg, Si, Sc and V, when compared to the mean enrichment rate of the other elements of the same stars. We believe that the existence of these groups of stars with peculiar chemistry may be related to the accretion of planetary material on to stellar surfaces or may be due to production of the same chemical element by different nucleosynthetic sites.