Sample records for alkali olivine basalt

  1. Ultramafic inclusions and host alkali olivine basalts of the southern coastal plain of the Red Sea, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Ghent, Edward D.; Coleman, Robert Griffin; Hadley, Donald G.

    1979-01-01

    A variety of mafic and ultramafic inclusions occur within the pyroclastic components of the Al Birk basalt, erupted on the southern Red Sea coastal plain of Saudi Arabia from Pleistocene time to the present. Depleted harzburgites are the only inclusions contained within the basalts that were erupted through Miocene oceanic crust (15 km thick) in the vicinity of Jizan, whereas to the north in the vicinity of Al Birk, alkali basalts that were erupted through a thicker Precambrian crust (48 km thick) contain mixtures of harzburgites, cumulate gabbro, and websterite inclusions accompanied by large (> 2 cm) megacrysts of glassy alumina-rich clinopyroxene, plagioclase, and spinel. Microprobe analyses of individual minerals from the harzburgites, websterites, and cumulate gabbros reveal variations in composition that can be related to a complex mantle history during the evolution of the alkali basalts. Clinopyroxene and plagioclase megacrysts may represent early phases that crystallized from the alkali olivine basalt magma at depths less than 35 km. Layered websterites and gabbros with cumulate plagioclase and clinopyroxene may represent continuing crystallization of the alkali olivine basalt magma in the lower crust when basaltic magma was not rapidly ascending. It is significant that the megacrysts and cumulate inclusions apparently form only where the magmas have traversed the Precambrian crust, whereas the harzburgite-bearing basalts that penetrated a much thinner Miocene oceanic crust reveal no evidence of mantle fractionation. These alkali olivine basalts and their contained inclusions are related in time to present-day rifting in the Red Sea axial trough. The onshore, deep-seated, undersaturated magmas are separated from the shallow Red Sea rift subalkaline basalts by only 170 km. The contemporaneity of alkaline olivine and subalkaline basalts requires that they must relate directly to the separation of the Arabian plate from the African plate.

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

    NASA Astrophysics Data System (ADS)

    Saadat, Saeed; Stern, Charles R.

    2012-05-01

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

  3. The solubility of olivine in basaltic liquids - An ionic model

    NASA Technical Reports Server (NTRS)

    Herzberg, C. T.

    1979-01-01

    A model is presented which enables the temperature at which olivine is in equilibrium with any alkali-depleted basaltic compound to be calculated to within + or - 30 C. It is noted that the error increases substantially when applied to terrestrial basalts which contain several weight percent alkalis. In addition the model predicts and quantifies the reduced activity of SiO4(4-) monomers due to increasing SiO2 concentrations in the melt. It is shown that the coordination of alumina in melts which precipitate olivine only appears to be dominantly octahedral, while titanium acts as a polmerizing agent by interconnecting previously isolated SiO4(4-) monomers. It is concluded that the model is sufficiently sensitive to show that there are small repulsive forces between Mg(2+) and calcium ions which are in association with normative diopside in the melt.

  4. Mantle xenolith-xenocryst-bearing monogenetic alkali basaltic lava field from Kutch Basin, Gujarat, Western India: Estimation of magma ascent rate

    NASA Astrophysics Data System (ADS)

    Ray, Arijit; Hatui, Kalyanbrata; Paul, Dalim Kumar; Sen, Gautam; Biswas, S. K.; Das, Brindaban

    2016-02-01

    Kutch rift basin of northwestern India is characterized by a topography that is controlled by a number of fault controlled uplifted blocks. Kutch Mainland Uplift, the largest uplifted block in the central part of the basin, contains alkali basalt plugs and tholeiitic basalt flows of the Deccan age. Alkali plugs often contain small, discoidal mantle xenoliths of spinel lherzolite and spinel wehrlite composition. Olivine occurs as xenocrysts (coarse, fractured, broken olivine grains with embayed margin; Fo> 90), phenocrysts (euhedral, smaller, and less forsteritic ~ Fo80), and as groundmass grains (small, anhedral, Fo75) in these alkali basalts. In a few cases, the alkali plugs are connected with feeder dykes. Based on the width of feeder dykes, on the sizes of the xenocrysts and xenoliths, thickness of alteration rim around olivine xenocryst, we estimate that the alkali magmas erupted at a minimum speed of 0.37 km per hour. The speed was likely greater because of the fact that the xenoliths broke up into smaller fragments as their host magma ascended through the lithosphere.

  5. Olivine-hosted Melt Inclusions: Insights into Highly Explosive Basaltic Volcanism from Alkali-rich Magma at Sunset Crater, AZ

    NASA Astrophysics Data System (ADS)

    Allison, C. M.; Roggensack, K.; Clarke, A. B.

    2017-12-01

    Sunset Crater volcano, an alkali basalt scoria cone in northern Arizona, erupted ca. 1085 AD, producing a large tephra blanket through sub-Plinian activity during its most explosive period. Primary melt inclusions (MIs) in free olivine crystals from the tephra were analyzed to study magma characteristics and storage conditions. We compare MIs from the early-erupted Strombolian deposit to those of sub-Plinian units to identify magma properties related to eruptive style. All MIs are faceted and closely similar in composition exhibiting minor post entrapment crystallization (3-15%). MIs are relatively dry (0.5-1.5 wt% H2O) but CO2-rich (1,200-3000 ppm). Most MIs contain >1 wt% H2O and >2,000 ppm CO2. MI vapor bubbles are ubiquitous in Sunset Crater samples ranging in size from 1 to 10 vol% of the MI in typical samples or 3 vol% on average. However, based on MI shrinkage caused by the decrease of olivine and melt densities with lower temperatures, only bubbles smaller than 3 vol% can result from post-entrapment cooling alone. We conclude that larger MI bubbles likely include volume contributions from pre-entrapment vapor. Raman spectroscopy, calibrated with synthetic CO2 inclusions, shows that the bubbles contain CO2 vapor and carbonate crystals have been observed on the bubble walls. Total MI CO2 contents, representing dissolved CO2 plus vapor bubble (if less than 3 vol% in size), range up to 4500 ppm. If no size constraint is applied to the vapor bubbles, the maximum total CO2 content (dissolved + vapor) reaches 6,500 ppm. These volatile abundances exceed the current experimental data on volatile solubility in alkali basalts. Fluid-saturated H2O-CO2 solubility experiments at 1200 °C between 400 and 600 MPa were conducted on the bulk Sunset Crater composition to account for the enhanced CO2 solubility of alkali-rich magma and accurately constrain solubility. This experimental data and the resulting calibrated thermodynamic model, indicates that MIs record depths up

  6. Anhydrous PT phase relations of an Aleutian high-MgO basalt: an investigation of the role of olivine-liquid reaction in the generation of arc high-alumina basalts

    NASA Astrophysics Data System (ADS)

    Draper, David S.; Johnston, A. Dana

    1992-12-01

    We report results of anhydrous 1 atm and piston-cylinder experiments on ID16, an Aleutian high-magnesia basalt (HMB), designed to investigate potential petrogenetic links between arc high-alumina basalts (HABs) and less common HMBs. ID16 is multiply saturated with a plagioclase/spinel iherzolite mineral assemblage (olivine, plagioclase, clinopyroxene, orthopyroxene, spinel) immediately beneath the 12 kbar liquidus. Derivative liquids produced at high temperatures in the 10 20 kbar melting interval of ID16 have compositions resembling those published of many moderate-CaO HABs, although lower-temperature liquids are poorer in CaO and richer in alkalies than are typical HABs. Isomolar pseudoternary projections and numerical mass-balance modeling suggest that derivative melts of ID16 enter into a complex reaction relationship with olivine at 10 kbar and 1,200° C 1,150° C. We sought to test such a mechanism to explain the lack of liquidus olivine in anhydrous experiments on mafic high-alumina basalts such as SSS. 1.4 (Johnston 1986). These derivative liquids, however, do not resemble typical arc high-alumina basalts, suggesting that olivine-liquid reaction does not account for Johnston's (1986) observations. Instead, we suggest that olivine can be brought onto the liquidus of such compositions only through the involvement of H2O, which will affect the influence of bulk CaO, MgO, and Al2O3 contents on the identity of HAB liquidus phases (olivine or plagioclase) at pressures less than ˜12 kbar.

  7. 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

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  9. Characterization and petrologic interpretation of olivine-rich basalts at Gusev Crater, Mars

    USGS Publications Warehouse

    McSween, H.Y.; Wyatt, M.B.; Gellert, Ralf; Bell, J.F.; Morris, R.V.; Herkenhoff, K. E.; Crumpler, L.S.; Milam, K.A.; Stockstill, K.R.; Tornabene, L.L.; Arvidson, R. E.; Bartlett, P.; Blaney, D.; Cabrol, N.A.; Christensen, P.R.; Clark, B. C.; Crisp, J.A.; Des Marais, D.J.; Economou, T.; Farmer, J.D.; Farrand, W.; Ghosh, A.; Golombek, M.; Gorevan, S.; Greeley, R.; Hamilton, V.E.; Johnson, J. R.; Joliff, B.L.; Klingelhofer, G.; Knudson, A.T.; McLennan, S.; Ming, D.; Moersch, J.E.; Rieder, R.; Ruff, S.W.; Schrorder, C.; de Souza, P.A.; Squyres, S. W.; Wanke, H.; Wang, A.; Yen, A.; Zipfel, J.

    2006-01-01

    Rocks on the floor of Gusev crater are basalts of uniform composition and mineralogy. Olivine, the only mineral to have been identified or inferred from data by all instruments on the Spirit rover, is especially abundant in these rocks. These picritic basalts are similar in many respects to certain Martian meteorites (olivine-phyric shergottites). The olivine megacrysts in both have intermediate compositions, with modal abundances ranging up to 20-30%. Associated minerals in both include low-calcium and high-calcium pyroxenes, plagioclase of intermediate composition, iron-titanium-chromium oxides, and phosphate. These rocks also share minor element trends, reflected in their nickel-magnesium and chromium-magnesium ratios. Gusev basalts and shergottites appear to have formed from primitive magmas produced by melting an undepleted mantle at depth and erupted without significant fractionation. However, apparent differences between Gusev rocks and shergottites in their ages, plagioclase abundances, and volatile contents preclude direct correlation. Orbital determinations of global olivine distribution and compositions by thermal emission spectroscopy suggest that olivine-rich rocks may be widespread. Because weathering under acidic conditions preferentially attacks olivine and disguises such rocks beneath alteration rinds, picritic basalts formed from primitive magmas may even be a common component of the Martian crust formed during ancient and recent times. Copyright 2006 by the American Geophysical Union.

  10. Characterization and Petrologic Interpretation of Olivine-Rich Basalts at Gusev Crater, Mars

    NASA Technical Reports Server (NTRS)

    McSween, H. Y.; Wyatt, M. B.; Gellert, R.; Bell, J. F., III; Morris, R. V.; Herkenhoff, K. E.; Crumpler, L. S.; Milam, K. A.; Stockstill, K. R.; Tornabene, L. L.; hide

    2006-01-01

    Rocks on the floor of Gusev crater are basalts of uniform composition and mineralogy. Olivine, the only mineral to have been identified or inferred from data by all instruments on the Spirit rover, is especially abundant in these rocks. These picritic basalts are similar in many respects to certain Martian meteorites (olivine-phyric shergottites). The olivine megacrysts in both have intermediate compositions, with modal abundances ranging up to 20-30%. Associated minerals in both include low-calcium and high-calcium pyroxenes, plagioclase of intermediate composition, iron-titanium-chromium oxides, and phosphate. These rocks also share minor element trends, reflected in their nickel-magnesium and chromium-magnesium ratios. Gusev basalts and shergottites appear to have formed from primitive magmas produced by melting an undepleted mantle at depth and erupted without significant fractionation. However, apparent differences between Gusev rocks and shergottites in their ages, plagioclase abundances, and volatile contents preclude direct correlation. Orbital determinations of global olivine distribution and compositions by thermal emission spectroscopy suggest that olivine-rich rocks may be widespread. Because weathering under acidic conditions preferentially attacks olivine and disguises such rocks beneath alteration rinds, picritic basalts formed from primitive magmas may even be a common component of the Martian crust formed during ancient and recent times.

  11. Chemical differences between small subsamples of Apollo 15 olivine-normative basalts

    NASA Technical Reports Server (NTRS)

    Shervais, J. W.; Vetter, S. K.; Lindstrom, M. M.

    1990-01-01

    Results are presented on the chemical and petrological characterization of nine samples of an Apollo 15 mare basalt suite. The results show that all nine samples are low-silica olivine normative basalts (ONBs) similar to those described earlier for low-silica ONBs from Apollo 15 site. The samples were found to vary in texture and grain size, from fine-grained intergranular or subophitic basalts to coarse-grained granular 'microgabbros'. Several displayed macroscopic heterogeneity. Variation diagrams show that the overall trend of the data is consistent with the fractionation of olivine (plus minor Cr-spinel) from a high-MgO parent magma.

  12. A New Spinel-Olivine Oxybarometer: Near-Liquidus Partitioning of V between Olivine-Melt, Spinel-Melt, and Spinel-Olivine in Martian Basalt Composition Y980459 as a Function of Oxygen Fugacity

    NASA Technical Reports Server (NTRS)

    Papike, J. J.; Le, L.; Burger, P. V.; Shearer, C. K.; Bell, A. S.; Jones, J.

    2013-01-01

    Our research on valence state partitioning began in 2005 with a review of Cr, Fe, Ti, and V partitioning among crystallographic sites in olivine, pyroxene, and spinel [1]. That paper was followed by several on QUE94201 melt composition and specifically on Cr, V, and Eu partitioning between pyroxene and melt [2-5]. This paper represents the continuation of our examination of the partitioning of multivalent V between olivine, spinel, and melt in martian olivine-phyric basalts of Y980459 composition [6, 7]. Here we introduce a new, potentially powerful oxybarometer, V partitioning between spinel and olivine, which can be used when no melt is preserved in the meteorite. The bulk composition of QUE94201 was ideal for our study of martian pyroxene-phyric basalts and specifically the partitioning between pyroxene-melt for Cr, V, and Eu. Likewise, bulk composition Y980459 is ideal for the study of martian olivine-phyric basalts and specifically for olivine-melt, spinel-melt, and spinel-olivine partitioning of V as a function of oxygen fugacity.

  13. Systematics of Ni, Co, Cr and V in Olivine from Planetary Melt Systems: Martian Basalts

    NASA Technical Reports Server (NTRS)

    Herd, C. D. K.; Jones, J. H.; Shearer, C. K.; Papike, J. J.

    2001-01-01

    Secondary Ion Mass Spectrometry (SIMS) data for Ni, Co, Cr, and V in olivine in martian basalts is compared to data from lunar and terrestrial basalts. We use experimentally-derived and published D values to calculate as-yet unsampled, olivine-bearing, non-cumulus melt compositions. Additional information is contained in the original extended abstract.

  14. Cotectic proportions of olivine and spinel in olivine-tholeiitic basalt and evaluation of pre-eruptive processes

    USGS Publications Warehouse

    Roeder, Peter; Gofton, Emma; Thornber, Carl

    2006-01-01

    The volume %, distribution, texture and composition of coexisting olivine, Cr-spinel and glass has been determined in quenched lava samples from Hawaii, Iceland and mid-oceanic ridges. The volume ratio of olivine to spinel varies from 60 to 2800 and samples with >0·02% spinel have a volume ratio of olivine to spinel of approximately 100. A plot of wt % MgO vs ppm Cr for natural and experimental basaltic glasses suggests that the general trend of the glasses can be explained by the crystallization of a cotectic ratio of olivine to spinel of about 100. One group of samples has an olivine to spinel ratio of approximately 100, with skeletal olivine phenocrysts and small (<50 μm) spinel crystals that tend to be spatially associated with the olivine phenocrysts. The large number of spinel crystals included within olivine phenocrysts is thought to be due to skeletal olivine phenocrysts coming into physical contact with spinel by synneusis during the chaotic conditions of ascent and extrusion. A second group of samples tend to have large olivine phenocrysts relatively free of included spinel, a few large (>100 μm) spinel crystals that show evidence of two stages of growth, and a volume ratio of olivine to spinel of 100 to well over 1000. The olivine and spinel in this group have crystallized more slowly with little physical interaction, and show evidence that they have accumulated in a magma chamber.

  15. Network topology of olivine-basalt partial melts

    NASA Astrophysics Data System (ADS)

    Skemer, Philip; Chaney, Molly M.; Emmerich, Adrienne L.; Miller, Kevin J.; Zhu, Wen-lu

    2017-07-01

    The microstructural relationship between melt and solid grains in partially molten rocks influences many physical properties, including permeability, rheology, electrical conductivity and seismic wave speeds. In this study, the connectivity of melt networks in the olivine-basalt system is explored using a systematic survey of 3-D X-ray microtomographic data. Experimentally synthesized samples with 2 and 5 vol.% melt are analysed as a series of melt tubules intersecting at nodes. Each node is characterized by a coordination number (CN), which is the number of melt tubules that intersect at that location. Statistically representative volumes are described by coordination number distributions (CND). Polyhedral grains can be packed in many configurations yielding different CNDs, however widely accepted theory predicts that systems with small dihedral angles, such as olivine-basalt, should exhibit a predominant CN of four. In this study, melt objects are identified with CN = 2-8, however more than 50 per cent are CN = 4, providing experimental verification of this theoretical prediction. A conceptual model that considers the role of heterogeneity in local grain size and melt fraction is proposed to explain the formation of nodes with CN ≠ 4. Correctly identifying the melt network topology is essential to understanding the relationship between permeability and porosity, and hence the transport properties of partial molten mantle rocks.

  16. Evaluation of thermobarometry for spinel lherzolite fragments in alkali basalts

    NASA Astrophysics Data System (ADS)

    Ozawa, Kazuhito; Youbi, Nasrrddine; Boumehdi, Moulay Ahmed; McKenzie, Dan; Nagahara, Hiroko

    2017-04-01

    various method of estimation of ascent rate of mantle fragments in kimberlite and alkali basalt; one based on fluid dynamics of transportation of entrapped fragments by giving the maximum size and viscosity of magma as a minimum estimate (Spera, 1980) and the other by coupling depth of fragment residence before the entrapment in a magma and time scale of heating by the magma. The depth of entrapment, however, is the least known parameter for spinel lherzolite. Because of nearly adiabatic ascent of magmas loaded with solid fragments, all the fragments underwent the same heating and decompression history with difference in entrapment depth and thus heating duration, from which the depth of their residence just before the extraction may be estimated if ascent rate is known. Therefore, extent of chemical and textural modification induced by heating and decompression may provide independent test for pressure estimation. We have used several reactions for this purpose: (1) Mg-Fe exchange reaction between spinel and olivine (Ozawa, 1983; 1984), (2) Ca zoning in olivine (Takahashi, 1980), (3) partial dissolution of clinopyroxene, (4) partial dissolution of spinel, and (5) formation of melt frozen as glass, which is related to (3) and (4). The depth of melt generation is constrained to be deeper than 70km by modeling the trace element compositions of the host magmas using the methods of McKenzie and O'Nions (1991) and data from El Azzouzi et al. (2010). The host magmas can be produced by melting the convecting upper mantle without requirement of any input from the continental lithosphere. This is consistent with the positive gravity anomalies in the NW Africa showing shallow upwelling in this region allowing decompressional melting owing to the thinner lithosphere in the Middle Atlas.

  17. A dynamic melting model for the origin of Apollo 15 olivine-normative and quartz-normative mare basalts

    NASA Technical Reports Server (NTRS)

    Vetter, Scott K.; Shervais, John W.

    1993-01-01

    Early studies of mare basalts from the Apollo 15 site established that two distinct groups are represented: the olivine-normative basalts (ONB) and the quartz-normative basalts (QNB). The ONB and QNB suites are distinguished petrographically by their phenocryst assemblages (the ONB's are olivine-phyric, the QNB's are generally pyroxene-phyric) and chemically by their major element compositions: the QNB's are higher in SiO2 and MgO/FeO, and lower in FeO and TiO2 than ONB's with similar MgO contents. Experimental data show that the QNB suite is derived from a more magnesian, olivine-normative parent magma, a conclusion which is supported by the recent discovery of high-SiO2 olivine-normative basalt clasts in breccia 15498. The high-SiO2 ONB's fall on olivine control lines with primitive QNB's, and least-squares mixing calculations are consistent with the high-SiO2 ONB's being parental to the more evolved QNB suite. These high-SiO2 ONB's are included as part of the 'QNB suite'. Our major element modeling results also are consistent with the conclusions of earlier studies which showed that the ONB and QNB suites cannot be related to one another by low pressure crystal fractionation. The combination of high Mg#, high SiO2, and low TiO2 in the QNB suite precludes a relationship to the ONB suite by simple removal of liquidus minerals (olivine and pigeonite). Despite these significant differences in petrography and major element composition, both groups have nearly identical trace element concentrations and chondrite-normalized abundance patterns. The major question to be addressed by any petrogenetic model for Apollo 15 mare basalts is how to form mare basalt suites with distinctly different major element characteristics but nearly identical trace element compositions. The similarity in trace element concentrations imply compositionally similar source regions and similar percent melting, but these conclusions are not easily reconciled with the observed differences in

  18. Reaction microtextures in entrapped xenoliths in alkali basalts from the Deccan large igneous province, India: Implications to the origin and evolution

    NASA Astrophysics Data System (ADS)

    Chattopadhaya, Soumi; Ghosh, Biswajit; Morishita, Tomoaki; Nandy, Sandip; Tamura, Akihiro; Bandyopadhyay, Debaditya

    2017-05-01

    The onset of the end-Mesozoic continental rift magmatism in the Deccan volcanic province (DVP), India is marked by alkali magmatism. Lithospheric fragments occurring as xenoliths/xenocrysts entrapped in alkaline basalts from the Kutch area of the DVP preserve reaction microtextures giving an insight into the processes linked to their origin. We interpret the flower texture, an aggregate of systematically arranged tiny diopside crystals, as a product of interactions between ghost quartz xenocrysts with alkaline silica-undersaturated melt. The mantle xenoliths, mostly represented by spinel lherzolites and wehrlites have been infiltrated by melt. The orthopyroxenes present at the margin of the xenoliths or in contact with infiltrated melt exhibit a coronal texture composed of olivine, clinopyroxene and glass around them. The compositions of cores of primary olivines at places retain mantle signatures, whereas, the margins are reequilibrated. Secondary olivines and clinopyroxenes at reaction coronas have a wide range of compositions. Primary clinopyroxenes and spinels in close vicinity to the orthopyroxene corona display a sieve texture defined by clear inclusion-free cores and a compositionally different spongy altered rim with worm-shaped or bubbly inclusions dominantly filled with glass. The rims are marked with higher Ca, Mg-lower Na, Al for clinopyroxenes and higher Ti, Cr-lower Mg, Al for spinels in comparison to their cores. The coronal texture around orthopyroxenes and spongy texture in clinopyroxenes and spinels in these xenoliths are interpreted to be genetically linked. The silicate glasses in the xenoliths show large compositional variations and they are much more siliceous and alkali-rich in comparison to the host basalts. The petrography and mineral chemistry suggest host magma-peridotite interaction during or after the entrainment of the xenoliths, corroborating well with the experimental findings.

  19. 57Fe Mössbauer spectroscopy of mineral assemblages in mantle spinel lherzolites from Cenozoic alkali basalt, eastern China: Petrological applications

    NASA Astrophysics Data System (ADS)

    Hao, Xi-Luo; Li, Yi-Liang

    2013-01-01

    Mineral assemblages in spinel lherzolite xenoliths from the Cenozoic alkali basalt of eastern China were analyzed by 57Fe Mössbauer spectroscopy for Fe3+/ΣFe and distribution of Fe2+/Fe3+ in non-equivalent crystal cites. Orthopyroxene, clinopyroxene and spinel have 0.08-0.13, 0.19-0.31 and 0.13-0.23 Fe3+/ΣFe, respectively. The cation-exchange equilibrium temperatures, Fe3+ partition coefficient and oxygen fugacity of the upper mantle peridotites were calculated. The equilibrium temperatures are between 1103 K and 1405 K consistent with those reported elsewhere. The oxygen fugacities of spinel lherzolites calculated with olivine-orthopyroxene-spinel (ΔlogƒO2 from - 1.1 to 0) and clinopyroxene-olivine-orthopyroxene oxybarometers (ΔlogƒO2 from - 2.0 to 0.7) are consistent with previously reported upper mantle values.

  20. Rates of mineral dissolution and carbonation in peridotite and basalt

    NASA Astrophysics Data System (ADS)

    Kelemen, P. B.; Matter, J. M.

    2009-12-01

    used a relatively high ratio of olivine:fluid (1:4), (c) they generally used high fluid NaCl contents, and (d) they consistently used high NaHCO3 and/or KHCO3 (alkali-bicarbonate) concentrations. In agreement with the ASU group, we consider that alkali-bicarbonate is the crucial catalyst, provided PCO2 is high.This raises the question of whether alkali-carbonate could also catalyze labradorite and basalt carbonation. ARC and ASU data extrapolated to low T and low PCO2 agree with natural carbonation rates in Oman. Our geological observations suggest that higher temperature peridotite carbonation went to completion (all Mg as MgCO3, all Si as quartz), perhaps because reaction-driven cracking maintained reactive surface area and permeability despite formation of reaction products in pore space and armoring of remaining olivine reactants. We are not aware of comparable observations on present-day carbonation of basalt. (1) Kelemen & Matter, PNAS 2008 (2) O’Connor et al., DOE Final Report ARC-TR-04-002, 2004 (3) Gerdemann et al., Environ. Sci. Technol. 2007 (4) Chizmeshya et al., DOE Final Report 924162, 2007

  1. Temperature dependence of sulfide and sulfate solubility in olivine-saturated basaltic magmas

    NASA Astrophysics Data System (ADS)

    Beermann, O.; Botcharnikov, R. E.; Holtz, F.; Diedrich, O.; Nowak, M.

    2011-12-01

    The sulfur concentration at pyrrhotite- and anhydrite-saturation in primitive hydrous basaltic melt of the 2001-2002 eruption of Mt. Etna was determined at 200 MPa, T = 1050-1250 °C and at log fO 2 from FMQ to FMQ+2.2 (FMQ is Fayalite-Magnetite-Quartz oxygen buffer). At 1050 °C Au sample containers were used. A double-capsule technique, using a single crystal olivine sample container closed with an olivine piston, embedded in a sealed Au 80Pd 20 capsule, was developed to perform experiments in S-bearing hydrous basaltic systems at T > 1050 °C. Pyrrhotite is found to be a stable phase coexisting with melt at FMQ-FMQ+0.3, whereas anhydrite is stable at FMQ+1.4-FMQ+2.2. The S concentration in the melt increases almost linearly from 0.12 ± 0.01 to 0.39 ± 0.02 wt.% S at FeS-saturation and from 0.74 ± 0.01 to 1.08 ± 0.04 wt.% S at anhydrite-saturation with T ranging from 1050-1250 °C. The relationships between S concentration at pyrrhotite and/or anhydrite saturation, MgO content of the olivine-saturated melt, T, and log fO 2 observed in this study and from previous data are used to develop an empirical model for estimating the magmatic T and fO 2 from the S and MgO concentrations of H 2O-bearing olivine-saturated basaltic melts. The model can also be used to determine maximum S concentrations, if fO 2 and MgO content of the melt are known. The application of the model to compositions of melt inclusions in olivines from Mt. Etna indicates that the most primitive magmas trapped in inclusions might have been stored at log fO 2 slightly higher than FMQ+1 and at T = 1100-1150 °C, whereas more evolved melts could have been trapped at T ⩽ 1100 °C. These values are in a good agreement with the estimates obtained by other independent methods reported in the literature.

  2. Spinel from Apollo 12 Olivine Mare Basalts: Chemical Systematics of Selected Major, Minor, and Trace Elements

    NASA Technical Reports Server (NTRS)

    Papike, J. J.; Karner, J. M.; Shearer, C. K.; Spilde, M. N.

    2002-01-01

    Spinels from Apollo 12 Olivine basalts have been studied by Electron and Ion microprobe techniques. The zoning trends of major, minor and trace elements provide new insights into the conditions under which planetary basalts form. Additional information is contained in the original extended abstract.

  3. The x ray microprobe determination of chromium oxidation state in olivine from lunar basalt and kimberlitic diamonds

    NASA Technical Reports Server (NTRS)

    Sutton, S. R.; Bajt, S.; Rivers, M. L.; Smith, J. V.

    1993-01-01

    The synchrotron x-ray microprobe is being used to obtain oxidation state information on planetary materials with high spatial resolution. Initial results on chromium in olivine from various sources including laboratory experiments, lunar basalt, and kimberlitic diamonds are reported. The lunar olivine was dominated by Cr(2+) whereas the diamond inclusions had Cr(2+/Cr(3+) ratios up to about 0.3. The simpliest interpretation is that the terrestrial olivine crystallized in a more oxidizing environment than the lunar olivine.

  4. Rb-Sr and Sm-Nd Studies of Olivine-Phyric Shergottites RBT 04262 and LAR 06319: Isotopic Evidence for Relationship to Enriched Basaltic Shergottites

    NASA Technical Reports Server (NTRS)

    Nyquist, L.E.; Shih, C.-Y.; Reese, Y.

    2009-01-01

    RBT 04262 and LAR 06319 are two Martian meteorites recently discovered in Antarctica. Both contain abundant olivines, and were classified as olivine-phyric shergottites. A detailed petrographic study of RBT 04262 suggested it should be reclassified as a lherzolitic shergottite. However, the moderately LREE-depleted REE distribution pattern indicated that it is closely related to enriched basaltic shergottites like Shergotty, Zagami, Los Angeles, etc. In earlier studies of a similarly olivinephyric shergottite NWA 1068 which contains 21% modal olivine, it was shown that it probably was produced from an enriched basaltic shergottite magma by olivine accumulation . As for LAR 06319, recent petrographic studies suggested that it is different from either lherzolitic shergottites or the highly LREE-depleted olivine-phyric shergottites. We performed Rb-Sr and Sm-Nd isotopic analyses on RBT 04262 and LAR 06319 to determine their crystallization ages and Sr and Nd isotopic signatures, and to better understand the petrogenetic relationships between them and other basaltic, lherzolitic and depleted olivine-phyric shergottites.

  5. Reduced chromium in olivine grains from lunar basalt 15555 - X-ray Absorption Near Edge Structure (XANES)

    NASA Technical Reports Server (NTRS)

    Sutton, S. R.; Jones, K. W.; Gordon, B.; Rivers, M. L.; Bajt, S.; Smith, J. V.

    1993-01-01

    The oxidation state of Cr in 200-micron regions within individual lunar olivine and pyroxene grains from lunar basalt 15555 was inferred using X-ray Absorption Near Edge Structure (XANES). Reference materials had previously been studied by optical absorption spectroscopy and included Cr-bearing borosilicate glasses synthesized under controlled oxygen fugacity and Cr-doped olivines. The energy dependence of XANES spectral features defined by these reference materials indicated that Cr is predominantly divalent in the lunar olivine and trivalent in the pyroxene. These results, coupled with the apparent f(02)-independence of partitioning coefficients for Cr into olivine, imply that the source magma was dominated by divalent Cr at the time of olivine crystallization.

  6. Estimates of olivine-basaltic melt electrical conductivity using a digital rock physics approach

    NASA Astrophysics Data System (ADS)

    Miller, Kevin J.; Montési, Laurent G. J.; Zhu, Wen-lu

    2015-12-01

    Estimates of melt content beneath fast-spreading mid-ocean ridges inferred from magnetotelluric tomography (MT) vary between 0.01 and 0.10. Much of this variation may stem from a lack of understanding of how the grain-scale melt geometry influences the bulk electrical conductivity of a partially molten rock, especially at low melt fraction. We compute bulk electrical conductivity of olivine-basalt aggregates over 0.02 to 0.20 melt fraction by simulating electric current in experimentally obtained partially molten geometries. Olivine-basalt aggregates were synthesized by hot-pressing San Carlos olivine and high-alumina basalt in a solid-medium piston-cylinder apparatus. Run conditions for experimental charges were 1.5 GPa and 1350 °C. Upon completion, charges were quenched and cored. Samples were imaged using synchrotron X-ray micro-computed tomography (μ-CT). The resulting high-resolution, 3-dimensional (3-D) image of the melt distribution constitutes a digital rock sample, on which numerical simulations were conducted to estimate material properties. To compute bulk electrical conductivity, we simulated a direct current measurement by solving the current continuity equation, assuming electrical conductivities for olivine and melt. An application of Ohm's Law yields the bulk electrical conductivity of the partially molten region. The bulk electrical conductivity values for nominally dry materials follow a power-law relationship σbulk = Cσmeltϕm with fit parameters m = 1.3 ± 0.3 and C = 0.66 ± 0.06. Laminar fluid flow simulations were conducted on the same partially molten geometries to obtain permeability, and the respective pathways for electrical current and fluid flow over the same melt geometry were compared. Our results indicate that the pathways for flow fluid are different from those for electric current. Electrical tortuosity is lower than fluid flow tortuosity. The simulation results are compared to existing experimental data, and the potential

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

    NASA Astrophysics Data System (ADS)

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

    2018-03-01

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

  8. Determination of Oxygen Fugacity using Olivine-Melt Equilibrium: Implications for the Redox States of Mid-Ocean Ridge Basalt, Ocean Island Basalt, and Island Arc Basalt Mantle Source Regions

    NASA Astrophysics Data System (ADS)

    Peterman, K. J.; Bryson, S.; Rilling-Hall, S.; Barton, M.

    2017-12-01

    In order to connect volcanic rocks to their mantle sources, it is essential to consider redox equilibria and their dependence on temperature, pressure, chemical composition, and oxygen fugacity. Oxygen fugacity (fO2) is an intensive variable that strongly affects the behavior of those elements in magmas that are sensitive to changes in redox state, such as Fe, and therefore Mg-Fe silicates, such as olivine. Since fO2 plays an important role in fractional crystallization, in principle it is possible to estimate fO2 from analyses of olivine in equilibrium with the melt. This research describes a new method based on this principle called the Olivine-Melt Equilibrium Method. The Fe3+ and Fe2+ contents of melt in equilibrium with olivine are calculated from the relationship of Gee and Sack (1988) that describes the partitioning of Mg and Fe2+ between olivine and melt. The Fe3+ and Fe2+ contents of the melt are then used to calculate the fO2 at which olivine and melt are in equilibrium using the model of Kress and Carmichael (1991) for the relationship between Fe3+/Fe2+ , fO2, T, P, and melt composition. We have calculated oxygen fugacities from published analyses of coexisting glass and olivine pairs in 1020 samples from three different tectonic settings. The results (expressed as ΔFMQ) for Mid-Ocean Ridge Basalts from the Mid-Atlantic Ridge (-1.55 ± 0.75), the East Pacific Rise (-0.65 ± 0.51), the Juan de Fuca Ridge (-0.77 ± 0.42), and the Galápagos Spreading Center (+0.08 ± 0.48) agree with results obtained using other methods and average -1.09 ± 0.89. Ocean Island Basalts from Iceland and the Galápagos Islands (ΔFMQ = -0.43 ± 0.71 and -0.33 ± 0.35 respectively) also yield values consistent with those obtained by other methods and fall in the same range as MORB. However, lavas from the Canary Islands are more oxidized than typical MORB and OIB, with values (average = +0.68 ± 0.52) approaching those for island arc magmas. We obtain ΔFMQ = +1.03 ± 0.52 for

  9. Basalt-trachybasalt samples in Gale Crater, Mars

    NASA Astrophysics Data System (ADS)

    Edwards, Peter H.; Bridges, John C.; Wiens, Roger; Anderson, Ryan; Dyar, Darby; Fisk, Martin; Thompson, Lucy; Gasda, Patrick; Filiberto, Justin; Schwenzer, Susanne P.; Blaney, Diana; Hutchinson, Ian

    2017-11-01

    The ChemCam instrument on the Mars Science Laboratory (MSL) rover, Curiosity, observed numerous igneous float rocks and conglomerate clasts, reported previously. A new statistical analysis of single-laser-shot spectra of igneous targets observed by ChemCam shows a strong peak at 55 wt% SiO2 and 6 wt% total alkalis, with a minor secondary maximum at 47-51 wt% SiO2 and lower alkali content. The centers of these distributions, together with the rock textures, indicate that many of the ChemCam igneous targets are trachybasalts, Mg# = 27 but with a secondary concentration of basaltic material, with a focus of compositions around Mg# = 54. We suggest that all of these igneous rocks resulted from low-pressure, olivine-dominated fractionation of Adirondack (MER) class-type basalt compositions. This magmatism has subalkaline, tholeiitic affinities. The similarity of the basalt endmember to much of the Gale sediment compositions in the first 1000 sols of the MSL mission suggests that this type of Fe-rich, relatively low-Mg#, olivine tholeiite is the dominant constituent of the Gale catchment that is the source material for the fine-grained sediments in Gale. The similarity to many Gusev igneous compositions suggests that it is a major constituent of ancient Martian magmas, and distinct from the shergottite parental melts thought to be associated with Tharsis and the Northern Lowlands. The Gale Crater catchment sampled a mixture of this tholeiitic basalt along with alkaline igneous material, together giving some analogies to terrestrial intraplate magmatic provinces.

  10. Basalt-trachybasalt samples in Gale Crater, Mars

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

    Edwards, Peter H.; Bridges, John C.; Wiens, Roger Craig

    The ChemCam instrument on the Mars Science Laboratory (MSL) rover, Curiosity, observed numerous igneous float rocks and conglomerate clasts, reported previously. A new statistical analysis of single-laser-shot spectra of igneous targets observed by ChemCam shows a strong peak at ~55 wt% SiO 2 and 6 wt% total alkalis, with a minor secondary maximum at 47–51 wt% SiO 2 and lower alkali content. The centers of these distributions, together with the rock textures, indicate that many of the ChemCam igneous targets are trachybasalts, Mg# = 27 but with a secondary concentration of basaltic material, with a focus of compositions around Mg#more » = 54. We suggest that all of these igneous rocks resulted from low-pressure, olivine-dominated fractionation of Adirondack (MER) class-type basalt compositions. This magmatism has subalkaline, tholeiitic affinities. The similarity of the basalt endmember to much of the Gale sediment compositions in the first 1000 sols of the MSL mission suggests that this type of Fe-rich, relatively low-Mg#, olivine tholeiite is the dominant constituent of the Gale catchment that is the source material for the fine-grained sediments in Gale. The similarity to many Gusev igneous compositions suggests that it is a major constituent of ancient Martian magmas, and distinct from the shergottite parental melts thought to be associated with Tharsis and the Northern Lowlands. Finally, the Gale Crater catchment sampled a mixture of this tholeiitic basalt along with alkaline igneous material, together giving some analogies to terrestrial intraplate magmatic provinces.« less

  11. Basalt-trachybasalt samples in Gale Crater, Mars

    DOE PAGES

    Edwards, Peter H.; Bridges, John C.; Wiens, Roger Craig; ...

    2017-09-14

    The ChemCam instrument on the Mars Science Laboratory (MSL) rover, Curiosity, observed numerous igneous float rocks and conglomerate clasts, reported previously. A new statistical analysis of single-laser-shot spectra of igneous targets observed by ChemCam shows a strong peak at ~55 wt% SiO 2 and 6 wt% total alkalis, with a minor secondary maximum at 47–51 wt% SiO 2 and lower alkali content. The centers of these distributions, together with the rock textures, indicate that many of the ChemCam igneous targets are trachybasalts, Mg# = 27 but with a secondary concentration of basaltic material, with a focus of compositions around Mg#more » = 54. We suggest that all of these igneous rocks resulted from low-pressure, olivine-dominated fractionation of Adirondack (MER) class-type basalt compositions. This magmatism has subalkaline, tholeiitic affinities. The similarity of the basalt endmember to much of the Gale sediment compositions in the first 1000 sols of the MSL mission suggests that this type of Fe-rich, relatively low-Mg#, olivine tholeiite is the dominant constituent of the Gale catchment that is the source material for the fine-grained sediments in Gale. The similarity to many Gusev igneous compositions suggests that it is a major constituent of ancient Martian magmas, and distinct from the shergottite parental melts thought to be associated with Tharsis and the Northern Lowlands. Finally, the Gale Crater catchment sampled a mixture of this tholeiitic basalt along with alkaline igneous material, together giving some analogies to terrestrial intraplate magmatic provinces.« less

  12. Petrology of basalts from Loihi Seamount, Hawaii

    NASA Astrophysics Data System (ADS)

    Hawkins, James; Melchior, John

    1983-12-01

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

  13. Composition and origin of basaltic magma of the Hawaiian Islands

    USGS Publications Warehouse

    Powers, H.A.

    1955-01-01

    Silica-saturated basaltic magma is the source of the voluminous lava flows, erupted frequently and rapidly in the primitive shield-building stage of activity, that form the bulk of each Hawaiian volcano. This magma may be available in batches that differ slightly in free silica content from batch to batch both at the same and at different volcanoes; differentiation by fractionation of olivine does not occur within this primitive magma. Silica-deficient basaltic magma, enriched in alkali, is the source of commonly porphyritic lava flows erupted less frequently and in relatively negligible volume during a declining and decadent stage of activity at some Hawaiian volcanoes. Differentiation by fractionation of olivine, plagioclase and augite is evident among these lavas, but does not account for the silica deficiency or the alkali enrichment. Most of the data of Hawaiian volcanism and petrology can be explained by a hypothesis that batches of magma are melted from crystalline paridotite by a recurrent process (distortion of the equatorial bulge by forced and free nutational stresses) that accomplishes the melting only of the plagioclase and pyroxene component but not the excess olivine and more refractory components within a zone of fixed and limited depth. Eruption exhausts the supply of meltable magma under a given locality and, in the absence of more violent melting processes, leaves a stratum of crystalline refractory components. ?? 1955.

  14. An Interactive Computer Program for Simulating the Effects of Olivine Fractionation from Basaltic and Ultrabasic Liquids.

    ERIC Educational Resources Information Center

    Pearce, Thomas H.

    1983-01-01

    Describes interactive computer program (listing available from author) which simulates olivine fractionation from basaltic/ultrabasic liquid. The menu-driven nature of the program (for Apple II microcomputer) allows students to select ideal Rayleigh fractionation or equilibrium crystallization. (JN)

  15. Occurrence and mineral chemistry of high pressure phases, Portrillo basalt, southcentral New Mexico. M.S. Thesis. Final Technical Report, 1 Jun. 1978 - 31 May 1980

    NASA Technical Reports Server (NTRS)

    Hoffer, J. M.; Ortiz, T. S.

    1980-01-01

    Inclusions of clinopyroxenite, kaersutiteclinopyroxenite, kaersutite-rich inclusions, wehrlite and olivine-clinopyroxenite together with megacrysts of feldspar, kaersutite and spinel are found loose on the flanks of cinder cones, as inclusions within lava flows and within the cores of volcanic bombs in the Quaternary alkali-olivine basalt of the West Potrillo Mountains, southcentral New Mexico. Based on petrological and geochemical evidence the megacysts are interpreted to be phenocrysts which formed at great depth rather that xenocrysts of larger crystal aggregates. These large crystals are believed to have formed as stable phases at high temperature and pressure and have partially reacted with the basalt to produce subhedral to anhedral crystal boundaries. It can be demonstrated that the mafic and ultramafic crystal aggregates were derived from an alkali-basalt source rock generated in the mantle. The inclusions are believed to represent a cumulus body or bodies injected within the lower crust or upper mantle.

  16. Oxygen isotope heterogeneity and disequilibria of olivine crystals in large volume Holocene basalts from Iceland: Evidence for magmatic digestion and erosion of Pleistocene hyaloclastites

    NASA Astrophysics Data System (ADS)

    Bindeman, Ilya; Gurenko, Andrey; Sigmarsson, Olgeir; Chaussidon, Marc

    2008-09-01

    This work considers petrogenesis of the largest Holocene basaltic fissure eruptions of Iceland, which are also the largest in the world: Laki (1783-84 AD, 15 km 3), Eldgjá (934 AD, 18 km 3), Veidivötn (900, 1480 AD, multiple eruptions, >2 km 3), Núpahraun (ca. 4000 BP, >1 km 3) and Thjórsárhraun (ca 8000 BP, >20 km 3). We present oxygen isotope laser fluorination analyses of 55 individual and bulk olivine crystals, coexisting individual and bulk plagioclase phenocrysts, and their host basaltic glasses with average precision of better than 0.1‰ (1SD). We also report O isotope analyses of cores and rims of 61 olivine crystals by SIMS with average precision on single spots of 0.24‰ (1SD) in 13 samples coupled with electron microprobe data for major and trace elements in these olivines. Within each individual sample, we have found that basaltic glass is relatively homogeneous with respect to oxygen isotopes, plagioclase phenocrysts exhibit crystal to crystal variability, while individual olivines span from the values in equilibrium with the low-δ 18O matrix glass to those being three permil higher in δ 18O than the equilibrium. Olivine cores with maximum value of 5.2‰ are found in many of these basalts and suggest that the initial magma was equilibrated with normal-δ 18O mantle. No olivines or their intracrystalline domains are found with bulk or spot value higher than those found in MORB olivines. The δ 18O variability of 0.3-3‰ exists for olivine grains from different lavas, and variable core-to-rim oxygen isotopic zoning is present in selected olivine grains. Many olivines in the same sample are not zoned, while a few grains are zoned with respect to oxygen isotopes and exhibit small core-to-core variations in Fe-Mg, Ni, Mn, Ca. Grains that are zoned in both Mg# and δ 18O exhibit positive correlation of these two parameters. Electron microprobe analysis shows that most olivines equilibrated with the transporting melt, and thin Fe-richer rim is

  17. Petrogenesis of Neogene basaltic volcanism associated with the Lut block, eastern Iran: Implication for tectonic and metallogenic evolution

    NASA Astrophysics Data System (ADS)

    Saadat, Saeed

    This dissertation presents petrochemical data concerning Neogene olivine basalts erupted both along the margins and within the micro-continental Lut block, eastern Iran, which is a part of the active Alpine-Himalayan orogenic belt. These data demonstrate the following: (1) Basalts that erupted from small monogenetic parasitic cones around the Bazman stratovolcano, Makran arc area, in the southern Lut block, are low-Ti sub-alkaline olivine basalts. Enrichments of LILE relative to LREE, and depletions in Nb and Ta relatively to LILE, are similar to those observed for other convergent plate boundary arc magmas around the world and suggest that these basalts formed by melting of subcontinental mantle modified by dehydration of the subducted Oman Sea oceanic lithosphere. (2) Northeast of Iran, an isolated outcrop of Neogene/Quaternary alkali olivine basalt, containing mantle and crustal xenoliths, formed by mixing of small melt fractions from both garnet and spinel-facies mantle. These melts rose to the surface along localized pathways associated with extension at the junction between the N-S right-lateral strike-slip faults and E-W left-lateral strike slip faults. The spinel-peridotite mantle xenoliths contained in the basalts, which equilibrated in the subcontinental lithosphere at depths of 30 to 60 km and temperatures of 965°C to 1065°C, do not preserve evidence of extensive metasomatic enrichment as has been inferred for the mantle below the Damavand volcano further to the west in north-central Iran. (3) Neogene mafic rocks within the central Lut block represent the last manifestation of a much more extensive mid-Tertiary magmatic event. These basalts formed from both OIB-like asthenosphere and subcontinental lithosphere which preserved chemical characteristics inherited from mid-Tertiary subduction associated with the collision of the Arabian with the Eurasian plate and closing of the Neotethys Ocean. Neogene/Quternary alkali olivine basalts erupted mainly along

  18. Valence State Partitioning of Cr and V Between Olivine-Melt and Pyroxene-Melt in Experimental Basalts of a Eucritic Composition

    NASA Technical Reports Server (NTRS)

    Karner, J. M.; Jones, J. H.; Le, L.

    2017-01-01

    The partitioning of multivalent elements in basaltic systems can elucidate the oxygen fugacity (fO2) conditions under which basalts formed on planetary bodies (Earth, Moon, Mars, asteroids). Chromium and V are minor and trace elements in basaltic melts, partition into several minerals that crystallize from basaltic melts, exist in multiple valence states at differing fO2 conditions, and can therefore be used as oxybarometers for basaltic melts. Chromium is mostly 3+ in terrestrial basaltic melts at relatively high fO2 values (= IW+3.5), and mostly 2+ in melts at low fO2 values (= IW-1), such as those on the Moon and some asteroids. At intermediate fO2s, (i.e., IW-1 to IW+3.5), basaltic melts contain both Cr3+ and Cr2+. Vanadium in basaltic melts is mostly 4+ at high fO2, mostly 3+ at low fO2, and a mix of V3+ and V4+ at intermediate fO2 con-ditions. Understanding the partitioning of Cr and V into silicate phases with changing fO2 is therefore critical to the employment of Cr and V oxybarometers. In this abstract we examine the equilibrium partitioning of Cr and V between olivine/melt and pyroxene/melt in experimental charges of a eucritic composition produced at differing fO2 conditions. This study will add to the experimental data on DCr and DV (i.e., olivine/melt, pyroxene/melt) at differing fO2, and in turn these D values will be used to assess the fO2 of eucrite basalts and perhaps other compositionally similar planetary basalts.

  19. Major element chemistry of Apollo 14 mare basalt clasts and highland plutonic clasts from lunar breccia 14321: Comparison with neutron activation results

    NASA Technical Reports Server (NTRS)

    Shervais, John W.; Vetter, Scott K.

    1993-01-01

    Studies of lithic components in lunar breccias have documented a wide variety of rock types and magma suites which are not found among large, discrete lunar samples. Rock types found exclusively or dominantly as clasts in breccias include KREEP basalts, VHK mare basalts, high-alumina mare basalts, olivine vitrophyres, alkali anorthosites, and magnesian anorthosites and troctolites. These miniature samples are crucial in petrogenetic studies of ancient mare basalts and the highlands crust of the western nearside, both of which have been battered by basin-forming impacts and no longer exist as distinct rock units.

  20. Experimental partitioning of rare earth elements and scandium among armalcolite, ilmenite, olivine and mare basalt liquid

    NASA Technical Reports Server (NTRS)

    Irving, A. J.; Merrill, R. B.; Singleton, D. E.

    1978-01-01

    An experimental study was carried out to measure partition coefficients for two rare-earth elements (Sm and Tm) and Sc among armalcolite, ilmenite, olivine and liquid coexisting in a system modeled on high-Ti mare basalt 74275. This 'primitive' sample was chosen for study because its major and trace element chemistry as well as its equilibrium phase relations at atmospheric pressure are known from previous studies. Beta-track analytical techniques were used so that partition coefficients could be measured in an environment whose bulk trace element composition is similar to that of the natural basalt. Partition coefficients for Cr and Mn were determined in the same experiments by microprobe analysis. The only equilibrium partial melting model appears to be one in which ilmenite is initially present in the source region but is consumed by melting before segregation of the high-Ti mare basalt liquid from the residue.

  1. Angrites: A Volatile-rich Variety of Asteroidal Basalt (Except for Alkalis and Gallium!)

    NASA Astrophysics Data System (ADS)

    Warren, P. H.; Kallemeyn, G. W.

    1995-09-01

    Angrites are commonly viewed as extremely volatile-depleted, and a related notion is that they formed by differentiation of a very CAI-rich material [e.g., 1]. Partial melting experiments reportedly reproduce the bulk compositions (although not fassaite-rich mineralogy) of angrites with Allende as starting material [2], but highly CAI-rich parent materials are difficult to reconcile with isotopic and REE data [3,4]. Mittlefehldt and Lindstrom [5] inferred from the low Na/Al ratios of angrites that outgassing, and thus primordial magmatism, was more intense on their parent body than on the eucrite parent asteroid. Of seven elements that (a) have been adequately determined in angrites, and (b) are far more volatile (solar-nebula 50% condensation T [6] = 690-430 K) than the alkalis (1000-910 K), four are enriched, and none is significantly depleted, in average angrite compared to average eucrite or low-Ti mare basalt (Figure). Gallium, which is of intermediate volatility (830 K), is depleted to roughly the same extent as Na and K. Results for A881371 [3] are incomplete (Zn, 6 micrograms/g, is near INAA detection limit), but even based only on AdoR and the two LEW angrites, this pattern seems firmly established. Apparent gas cavities in A881371 [7] also suggest that volatiles are far from uniformly depleted. The only elements known to be depleted, as volatiles, by clearly significant factors in angrites versus eucrites or lunar basalts, are alkalis plus gallium. Besides being moderately volatile, a noteworthy characteristic shared among Ga and alkalis (and not shared with elements such as Br, Se, and Zn) is that these elements probably tend to partition into crustal feldspar during gross differentiation of small (low-pressure) bodies. If gallium + alkalis were depleted by a single process starting from "normal" chondritic material, that process would seem to require selective exposure of a feldspar-enriched region (i.e., crust) to extremely high temperature. Igneous

  2. Mafic mantle sources indicated by the olivine-spinifex basalt-ferropicrite lavas in the accreted Permian oceanic LIP fragments and Miocene low-Ni basalt and adakite lavas in central Japan

    NASA Astrophysics Data System (ADS)

    Ishiwatari, A.; Ichiyama, Y.; Yamazaki, R.; Katsuragi, T.; Tsuchihashi, H.

    2008-12-01

    Melting of mafic (eclogitic) rocks in the peridotite mantle diapir may be important to generate a large quantity of magma in a short period of time as required for the LIP basaltic magmatism (e.g. Takahashi et al. 1998; EPSL, 162, 63-). Ferropicritic rocks also occur in some LIPs, and Ichiyama et al. (2006; Lithos, 89, 47-) propose a non-peridotitic, Ti- and Fe-rich eclogitic source (recycled oceanic ferrogabbro?) entrained in the peridotitic LIP mantle plume for the origin of ferropicritic rocks, that occur with olivine-spinifex basalt (Ichiyama et al., 2007; Island Arc, 16, 493-) in a Permian LIP fragment that was captured in the Jurassic Tamba accretionary complex in central Japan. Although Ti-poor ferrokomatiitic magma might form through high- degree melting of a primitive chondritic mantle (25wt% MgO and 25wt% Fe+FeO), Ti- and HFSE-rich ferropicritic and meimechitic magmas can not form in this way. On the other hand, Miocene volcanic rocks distributed along the Japan Sea coast of central Japan also represent a product of large-scale arc magmatism that happened coeval to the spreading of the Japan Sea floor. The chemical and isotopic signatures of the magmas are consistent with the secular change of tectonic setting from continental arc (22- 20 Ma) to island arc (15-11 Ma) (Shuto et al. 2006; Lithos, 86, 1-). Some adakites have already been found from these Miocene volcanic rocks by Shuto"fs group, and mafic rock melting in either subducting slab or lower arc crust has been proposed. We have recently found a wide distribution of low-Ni basalt from Fukui City. The low-Ni basalt contains olivine phenocrysts which are one order of magnitude poorer in Ni (less than 0.02 wt% NiO at Fo87) than those in normal basalt (more than 0.2 wt% NiO at Fo87). The rock is also poor in bulk-rock Ni, rich in K and Ti, and may have formed from an olivine-free pyroxenitic source. Close association of adakite and low-Ni basalt with normal tholeiitic basalt, calc-alkaline andesite

  3. Flow in the western Mediterranean shallow mantle: Insights from xenoliths in Pliocene alkali basalts from SE Iberia (eastern Betics, Spain)

    NASA Astrophysics Data System (ADS)

    Hidas, Károly; Konc, Zoltán.; Garrido, Carlos J.; Tommasi, Andréa.; Vauchez, Alain; Padrón-Navarta, José Alberto; Marchesi, Claudio; Booth-Rea, Guillermo; Acosta-Vigil, Antonio; Szabó, Csaba; Varas-Reus, María. Isabel; Gervilla, Fernando

    2016-11-01

    Mantle xenoliths in Pliocene alkali basalts of the eastern Betics (SE Iberia, Spain) are spinel ± plagioclase lherzolite, with minor harzburgite and wehrlite, displaying porphyroclastic or equigranular textures. Equigranular peridotites have olivine crystal preferred orientation (CPO) patterns similar to those of porphyroclastic xenoliths but slightly more dispersed. Olivine CPO shows [100]-fiber patterns characterized by strong alignment of [100]-axes subparallel to the stretching lineation and a girdle distribution of [010]-axes normal to it. This pattern is consistent with simple shear or transtensional deformation accommodated by dislocation creep. One xenolith provides evidence for synkinematic reactive percolation of subduction-related Si-rich melts/fluids that resulted in oriented crystallization of orthopyroxene. Despite a seemingly undeformed microstructure, the CPO in orthopyroxenite veins in composite xenoliths is identical to those of pyroxenes in the host peridotite, suggesting late-kinematic crystallization. Based on these observations, we propose that the annealing producing the equigranular microstructures was triggered by melt percolation in the shallow subcontinental lithospheric mantle coeval to the late Neogene formation of veins in composite xenoliths. Calculated seismic properties are characterized by fast propagation of P waves and polarization of fast S waves parallel to olivine [100]-axis (stretching lineation). These data are compatible with present-day seismic anisotropy observations in SE Iberia if the foliations in the lithospheric mantle are steeply dipping and lineations are subhorizontal with ENE strike, implying dominantly horizontal mantle flow in the ENE-WSW direction within vertical planes, that is, subparallel to the paleo-Iberian margin. The measured anisotropy could thus reflect a lithospheric fabric due to strike-slip deformation in the late Miocene in the context of WSW tearing of the subducted south Iberian margin

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

    NASA Astrophysics Data System (ADS)

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

    2017-12-01

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

  5. Mare basalts on the Apennine Front and the mare stratigraphy of the Apollo 15 landing site

    NASA Technical Reports Server (NTRS)

    Ryder, Graham

    1989-01-01

    Olivine-normative mare basalts are present on the Apennine Front as crystalline particles and shocked or shock-melted fragments. Picritic basalts, which may be related to the olivine-normative basalts by olivine accumulation, not only occur on the Front but such samples so far recognized are confined to it. Mare volcanic and impact glasses also occur on the Front; all are olivine-normative, though none are quite the equivalent of the typical olivine-normative mare group. The quartz-normative mare basalts are not present (or are extremely rare) on the Front either as crystalline basalts or shocked or glass equivalents. These observations are consistent with the olivine-normative mare basalts being both local and the youngest flows at the site, and the fragments being emplaced on the Front by impacts. The picritic basalts raise the distinct possibility that the olivine-normative basalts also ponded on the Front. An influx of olivine-normative basalts from exotic sources (e.g., a ray from Aristillus) is inconsistent with their abundance, their dominance in the mare soil chemistry, and their age, isotopic, and trace element similarities with the quartz-normative basalts. However, the thermal histories of the olivine-normative basalts require elucidation.

  6. Moessbauer Mineralogy of Rock, Soil, and Dust at Gusev Crater, Mars: Spirit's Journey through Weakly Altered Olivine Basalt on the Plains and Pervasively Altered Basalt in the Columbia Hills

    NASA Technical Reports Server (NTRS)

    Morris, R. V.; Klingelhoefer, G.; Schroeder, C.; Rodionov, D. S.; Yen, A.; Ming, D. W.; deSouza, P. A., Jr.; Fleischer, I.; Wdowiak, T.; Gellert, R.; hide

    2006-01-01

    The Moessbauer spectrometer on Spirit measured the oxidation state of Fe, identified Fe-bearing phases, and measured relative abundances of Fe among those phases for surface materials on the plains and in the Columbia Hills of Gusev crater. Eight Fe-bearing phases were identified: olivine, pyroxene, ilmenite, magnetite, nanophase ferric oxide (npOx), hematite, goethite, and a Fe(3+)-sulfate. Adirondack basaltic rocks on the plains are nearly unaltered (Fe(3+)/Fe(sub T)<0.2) with Fe from olivine, pyroxene (Ol>Px), and minor npOx and magnetite. Columbia Hills basaltic rocks are nearly unaltered (Peace and Backstay), moderately altered (WoolyPatch, Wishstone, and Keystone), and pervasively altered (e.g., Clovis, Uchben, Watchtower, Keel, and Paros with Fe(3+)/Fe(sub T) approx.0.6-0.9). Fe from pyroxene is greater than Fe from olivine (Ol sometimes absent), and Fe(2+) from Ol+Px is 40-49% and 9-24% for moderately and pervasively altered materials, respectively. Ilmenite (Fe from Ilm approx.3-6%) is present in Backstay, Wishstone, Keystone, and related rocks along with magnetite (Fe from Mt approx. 10-15%). Remaining Fe is present as npOx, hematite, and goethite in variable proportions. Clovis has the highest goethite content (Fe from Gt=40%). Goethite (alpha-FeOOH) is mineralogical evidence for aqueous processes because it has structural hydroxide and is formed under aqueous conditions. Relatively unaltered basaltic soils (Fe(3+)/Fe(sub T) approx. 0.3) occur throughout Gusev crater (approx. 60-80% Fe from Ol+Px, approx. 10-30% from npOx, and approx. 10% from Mt). PasoRobles soil in the Columbia Hills has a unique occurrence of high concentrations of Fe(3+)-sulfate (approx. 65% of Fe). Magnetite is identified as a strongly magnetic phase in Martian soil and dust.

  7. Crystal preferred orientations of minerals from mantle xenoliths in alkali basaltic rocks form the Catalan Volcanic Zone (NE Spain)

    NASA Astrophysics Data System (ADS)

    Fernández-Roig, Mercè; Galán, Gumer; Mariani, Elisabetta

    2015-04-01

    Mantle xenoliths in alkali basaltic rocks from the Catalan Volcanic Zone, associated with the Neogene-Quaternary rift system in NE Spain, are formed of anhydrous spinel lherzolites and harzburgites with minor olivine websterites. Both peridotites are considered residues of variable degrees of partial melting, later affected by metasomatism, especially the harzburgites. These and the websterites display protogranular microstructures, whereas lherzolites show continuous variation between protogranular, porphyroclastic and equigranular forms. Thermometric data of new xenoliths indicate that protogranular harzburgites, lherzolites and websterites were equilibrated at higher temperatures than porphyroclastic and equigranular lherzolites. Mineral chemistry also indicates lower equilibrium pressure for porphyroclastic and equigranular lherzolites than for the protogranular ones. Crystal preferred orientations (CPOs) of olivine and pyroxenes from these new xenoliths were determined with the EBSD-SEM technique to identify the deformation stages affecting the lithospheric mantle in this zone and to assess the relationships between the deformation fabrics, processes and microstructures. Olivine CPOs in protogranular harzburgites, lherzolites and a pyroxenite display [010]-fiber patterns characterized by a strong point concentration of the [010] axis normal to the foliation and girdle distribution of [100] and [001] axes within the foliation plane. Olivine CPO symmetry in porphyroclastic and equigranular lherzolites varies continuously from [010]-fiber to orthorhombic and [100]-fiber types. The orthorhombic patterns are characterized by scattered maxima of the three axes, which are normal between them. The rare [100]-fiber patterns display strong point concentration of [100] axis, with normal girdle distribution of the other two axes, which are aligned with each other. The patterns of pyroxene CPOs are more dispersed than those of olivine, especially for clinopyroxene, but

  8. Discriminating between pyroxenite and peridotite sources for continental flood basalts (CFB) in southern Africa using olivine chemistry

    NASA Astrophysics Data System (ADS)

    Howarth, Geoffrey H.; Harris, Chris

    2017-10-01

    Continental Flood Basalts (CFB) result from voluminous outpourings of magma that often precede continental break-up. Notwithstanding the petrogenetic importance of CFBs, the nature of the mantle source for such magmas is contentious, particularly with regard to picrites with Ni-rich olivine phenocrysts. Previous studies have suggested that Ni-rich olivines associated with plume volcanism in regions of thickened (>90 km) lithosphere are related to either source mineralogy differences (peridotite versus pyroxenite) or change in olivine-melt partitioning due to pressure increase. In order to evaluate these two hypotheses, we present trace element data for olivines from the Karoo CFB Tuli and Mwenezi picrites and the Etendeka CFB Horingbaai/LTZ-L type picrites, all of which erupted in regions of thickened (>90 km) lithosphere in southern Africa. Karoo picrite olivines are Ni-rich, Ca- and Mn-poor, and have low (<1.4) 100*Mn/Fe. These compositions are consistent with a pyroxenitic source. Etendeka Horingbaai/LTZ-L picrite olivines do not show Ni-enrichment, but are characterized by high Al and Cr, and high (>1.4) 100*Mn/Fe, which is more consistent with high temperature melting of a dominantly peridotitic source. We also show that the Karoo and Etendeka olivines are characterized by distinct Mn/Zn ratios of <13 and >15, respectively. In addition, bulk rock geochemical data compilations and previously reported olivine δ18O for Karoo and Etendeka CFBs are discussed in order to further constrain source components based on previously described pyroxenite melt geochemical indices such as MgO-CaO systematics, FeO/MnO, Zn/Fe, and FC3MS (FeO/CaO-3*MgO/SiO2). These geochemical indices suggest a pyroxenite-dominated source for Karoo CFBs as well as for Etendeka ferropicrites whereas a peridotite-dominated source is indicated for Etendeka Horingbaai/LTZ-L type picrites analyzed in this study. Based on our data, Ni-enrichment of olivine in plume-related magmas in regions of

  9. Quantitative characterization of 3-dimensional melt distribution in partially molten olivine-basalt aggregates using X-ray synchrotron microtomography

    NASA Astrophysics Data System (ADS)

    Zhu, W.; Gaetani, G. A.; Fusseis, F.

    2009-12-01

    Quantitative knowledge of the distribution of small amounts of silicate melt in peridotite and of its influence on permeability are critical to our understanding of melt migration and segregation processes in the upper mantle. Estimates for the permeability of partially molten rock require 3D melt distribution at the grain-scale. Existing studies of melt distribution, carried out on 2D slices through experimental charges, have produced divergent models for melt distribution at small melt fractions. While some studies conclude that small amounts of melt are distributed primarily along triple junctions [e.g., Wark et al., 2003], others predict an important role for melt distribution along grain boundaries at low melt fractions [e.g., Faul 1997]. Using X-ray synchrotron microtomography, we have obtained the first high quality non-destructive imaging of 3D melt distribution in olivine-basalt aggregates. Textually equilibrated partially molten samples consisting of magnesian olivine plus 2, 5, 10, or 20% primitive basalt were synthesized at 1.5 GPa and 1350°C in experiments lasting 264-336 hours. Microtomographic images of melt distribution were obtained on cylindrical cores, 1 mm in diameter, at a spatial resolution of 1 micron. Textual information such as melt channel size, dihedral angle and channel connectivity was then quantified using AVIZO and MATLAB. Our results indicate that as melt fraction decreases, melt becomes increasingly distributed along 3 grain junctions, in agreement with theoretical predictions. We do not find significant amounts of melt along grain boundaries at low melt fractions. We found that the true dihedral angle ranges from 50 to 70°, in agreements with results using 2D microcopy. Comparison between the samples provides a quantitative characterization of how melt fraction affects melt distribution including connectivity. The geometrical data have been incorporated into our network model to obtain macroscale transport properties for

  10. Rare earth element contents and multiple mantle sources of the transform-related Mount Edgecumbe basalts, southeastern Alaska

    USGS Publications Warehouse

    Riehle, J.R.; Budahn, J.R.; Lanphere, M.A.; Brew, D.A.

    1994-01-01

    Pleistocene basalt of the Mount Edgecumbe volcanic field (MEF) is subdivided into a plagioclase type and an olivine type. Th/La ratios of plagioclase basalt are similar to those of mid-ocean-ridge basalt (MORB), whereas those of olivine basalt are of continental affinity. Rare earth element (REE) contents of the olivine basalt, which resemble those of transitional MORB, are modelled by 10-15% partial melting of fertile spinel-plagioclase lherzolite followed by removal of 8-13% olivine. It is concluded that olivine basalt originated in subcontinental spinel lherzolite and that plagioclase basalt may have originated in suboceanic lithosphere of the Pacific plate. -from Authors

  11. Crystallization kinetics of olivine-phyric shergottites

    NASA Astrophysics Data System (ADS)

    Ennis, Megan E.; McSween, Harry Y.

    2014-08-01

    Crystal size distribution (CSD) and spatial distribution pattern (SDP) analyses are applied to the early crystallizing phases, olivine and pyroxene, in olivine-phyric shergottites (Elephant moraine [EET] 79001A, Dar al Gani [DaG] 476, and dhofar [Dho] 019) from each sampling locality inferred from Mars ejection ages. Trace element zonation patterns (P and Cr) in olivine are also used to characterize the crystallization history of these Martian basalts. Previously reported 2-D CSDs for these meteorites are re-evaluated using a newer stereographically corrected methodology. Kinks in the olivine CSD plots suggest several populations that crystallized under different conditions. CSDs for pyroxene in DaG 476 and EET 79001A reveal single populations that grew under steady-state conditions; pyroxenes in Dho 019 were too intergrown for CSD analysis. Magma chamber residence times of several days for small grains to several months for olivine megacrysts are calculated using the CSD slopes and growth rates inferred from previous experimental data. Phosphorus imaging in olivines in DaG 476 and Dho 019 indicate rapid growth of skeletal, sector-zoned, or patchy cores, probably in response to delayed nucleation, followed by slow growth, and finally rapid dendritic growth with back-filling to form oscillatory zoning in rims. SPD analyses indicate that olivine and pyroxene crystals grew or accumulated in clusters rather than as randomly distributed grains. These data reveal complex solidification histories for Martian basalts, and are generally consistent with the formation at depth of olivine megacryst cores, which were entrained in ascending magmas that crystallized pyroxenes, small olivines, and oscillatory rims on megacrysts.

  12. Heterogeneity in small aliquots of Apolllo 15 olivine-normative basalt: Implications for breccia clast studies

    NASA Astrophysics Data System (ADS)

    Lindstrom, Marilyn M.; Shervais, John W.; Vetter, Scott K.

    1993-05-01

    Most of the recent advances in lunar petrology are the direct result of breccia pull-apart studies, which have identified a wide array of new highland and mare basalt rock types that occur only as clasts within the breccias. These rocks show that the lunar crust is far more complex than suspected previously, and that processes such as magma mixing and wall-rock assimilation were important in its petrogenesis. These studies are based on the implicit assumption that the breccia clasts, which range in size from a few mm to several cm across, are representative of the parent rock from which they were derived. In many cases, the aliquot allocated for analysis may be only a few grain diameters across. While this problem is most acute for coarse-grained highland rocks, it can also cause considerable uncertainty in the analysis of mare basalt clasts. Similar problems arise with small aliquots of individual hand samples. Our study of sample heterogeneity in 9 samples of Apollo 15 olivine normative basalt (ONB) which exhibit a range in average grain size from coarse to fine are reported. Seven of these samples have not been analyzed previously, one has been analyzed by INAA only, and one has been analyzed by XRF+INAA. Our goal is to assess the effects of small aliquot size on the bulk chemistry of large mare basalt samples, and to extend this assessment to analyses of small breccia clasts.

  13. Heterogeneity in small aliquots of Apolllo 15 olivine-normative basalt: Implications for breccia clast studies

    NASA Technical Reports Server (NTRS)

    Lindstrom, Marilyn M.; Shervais, John W.; Vetter, Scott K.

    1993-01-01

    Most of the recent advances in lunar petrology are the direct result of breccia pull-apart studies, which have identified a wide array of new highland and mare basalt rock types that occur only as clasts within the breccias. These rocks show that the lunar crust is far more complex than suspected previously, and that processes such as magma mixing and wall-rock assimilation were important in its petrogenesis. These studies are based on the implicit assumption that the breccia clasts, which range in size from a few mm to several cm across, are representative of the parent rock from which they were derived. In many cases, the aliquot allocated for analysis may be only a few grain diameters across. While this problem is most acute for coarse-grained highland rocks, it can also cause considerable uncertainty in the analysis of mare basalt clasts. Similar problems arise with small aliquots of individual hand samples. Our study of sample heterogeneity in 9 samples of Apollo 15 olivine normative basalt (ONB) which exhibit a range in average grain size from coarse to fine are reported. Seven of these samples have not been analyzed previously, one has been analyzed by INAA only, and one has been analyzed by XRF+INAA. Our goal is to assess the effects of small aliquot size on the bulk chemistry of large mare basalt samples, and to extend this assessment to analyses of small breccia clasts.

  14. The Age of Rift-Related Basalts in East Antarctica

    NASA Astrophysics Data System (ADS)

    Leitchenkov, G. L.; Belyatsky, B. V.; Kaminsky, V. D.

    2018-01-01

    The Lambert Rift, which is a large intracontinental rift zone in East Antarctica, developed over a long period of geological time, beginning from the Late Paleozoic, and its evolution was accompanied by magmatic activity. The latest manifestation of magmatism is eruption of alkaline olivine-leucite basalts on the western side of the Lambert Rift; Rb-Sr dating referred its time to the Middle Eocene, although its genesis remained vague. In order to solve this problem, we found geochronometer minerals in basaltic samples and 68 apatite grains appeared to be suitable for analysis. Their ages and ages of host basalts, determined by the U-Pb local method on the SIMS SHRIMP-II, were significantly different (323 ± 31 Ma) from those assumed earlier. This age corresponds to the earliest stage of crustal extension in East Antarctica and to most of Gondwana. The new data crucially change the ideas about the evolution of Lambert Rift and demonstrate the ambiguity of K-Ar dates of the alkali effusive formed under long-term rifting.

  15. Influence of H2O on Liquidus Temperatures of Primitive Basalts and Olivine-Liquid Thermometry.

    NASA Astrophysics Data System (ADS)

    Medard, E.; Grove, T. L.

    2005-12-01

    We have undertaken a systematic experimental study aimed at understanding the effect of water on olivine liquidus temperatures of primitive basalts. Experiments have been performed on a primitive tholeiitic basalt from Medicine Lake Volcano, California (sample 82-72f, Bartels et al. 1991). The dry liquidus has been characterized from 0.1 MPa to 1.2 GPa. The wet liquidus has been constrained to within 15 °C using water-saturated experiments performed in a MHC externally heated pressure vessel. Preliminary results show that the olivine-liquidus depression (i.e., the difference between dry and water-bearing liquidus) is essentially a linear function of the water content of the melt: ΔT = 560  X(HO0.5), where X(HO0.5) is the mole fraction of water, calculated on a single-cation oxide basis. For 82-72f, this roughly translates into a 30 °C / wt% H2O depression. Simple systems (e.g., diopside/H2O, albite/H2O) suggest that melt structure / composition may have an influence on H2O liquidus depression, and this potential influence is currently under investigation. Experimental phase equilibria and thermobarometry of primitive basalts provide the primary evidence for estimating melting conditions and thermal structures in the Earth's mantle. Assessing the influence of H2O is critical, because it is the dominant volatile component involved in igneous processes, and it has been shown to cause a significant reduction in liquidus temperatures. However, recent model parameterizations vary from very large effects at low H2O contents (about 75 °C at 1 wt% H2O, Falloon and Danyushevsky 2000) to linear effect of H2O vs liquidus temperature (about 25 °C at 1 wt% H2O, Sugawara 2000). Our experimental determination more closely approximates the latter model. A key consequence is that the presence of small amounts of water in MORB magmas (< 1wt%) will only have a very small effect (< 30 °C) on liquidus temperature determination for mid-ocean-ridges. For magmas that are more

  16. Settling and compaction of olivine in basaltic magmas: an experimental study on the time scales of cumulate formation

    NASA Astrophysics Data System (ADS)

    Schmidt, Max W.; Forien, Melanie; Solferino, Giulio; Bagdassarov, Nickolai

    2012-12-01

    A series of centrifuge-assisted settling experiments of 30 vol % olivine in 70 vol % basaltic melt was conducted to elucidate the formation mechanisms and time scales of gravitational cumulates. The settling experiments were performed in a centrifuging piston cylinder at 200-1,500 g, 1,270-1,280 °C, and 0.8-1.1 GPa on previously annealed and texturally equilibrated samples. The mechanical settling of the dense olivine suspension occurs at about 1/6 the speed of simple Stokes settling, resulting in a sedimentation exponent n = 4.1(6) in agreement with predictions from analogue systems. The porosity (φ m ) of the orthocumulate resulting from gravitational settling of crystals is about 54 % and formation times of olivine orthocumulates result to 0.1-10 m day-1 (for an initial crystal content of the melt of 1-5 % and grain sizes of 2-10 mm). After mechanical settling, olivine grains rest on each other, and further compaction occurs through pressure dissolution at grain contacts, olivine reprecipitation where olivine is in contact with melt, and concomitant expulsion of excess liquid from the cumulate layer. With centrifugation at 400 g for 50 h, porosities as low as 30.3 vol % were achieved. The olivine content at the bottom of the gravitational cumulate is 1 - φm ~ log(Δρ · h · a · t), where Δρ is the density difference between crystals and melt, h the crystal layer thickness, a the acceleration, and t the time of centrifuging. Compaction is hence proportional to effective stress integrated over time indicating that pressure dissolution is the dominant mechanism for chemical compaction. The compaction limit, that is the lowermost porosity to be reached by this mechanism, is calculated by equating the lithostatic and hydraulic pressure gradients in the cumulate and results to 3-5 % porosity for the experiments. Crystal size distribution curves and a growth exponent n of 3.1(3) indicate that diffusion-controlled Ostwald ripening is the dominant crystal growth

  17. Mantle and crustal contribution in the genesis of Recent basalts from off-rift zones in Iceland: Constraints from Th, Sr and O isotopes

    NASA Astrophysics Data System (ADS)

    Sigmarsson, Olgeir; Condomines, Michel; Fourcade, Serge

    1992-05-01

    Along the two volcanic off-rift zones in Iceland, the Sn˦fellsnes volcanic zone (SNVZ) and the South Iceland volcanic zone (SIVZ), geochemical parameters vary regularly along the strike towards the centre of the island. Recent basalts from the SNVZ change from alkali basalts to tholeiites where the volcanic zone reaches the active rift axis, and their 87Sr/ 86Sr and Th/U ratios decrease in the same direction. These variations are interpreted as the result of mixing between mantle melts from two distinct reservoirs below Sn˦fellsnes. The mantle melt would be more depleted in incompatible elements, but with a higher 3He/ 4He ratio ( R/Ra≈ 20) beneath the centre of Iceland than at the tip of the Sn˦fellsnes volcanic zone ( R/Ra≈ 7.5). From southwest to northeast along the SIVZ, the basalts change from alkali basalts to FeTi basalts and quartz-normative tholeiites. The Th/U ratio of the Recent basalts increases and both ( 230Th/ 232Th ) and δ 18O values decrease in the same direction. This reflects an important crustal contamination of the FeTi-rich basalts and the quartz tholeiites. The two types of basalts could be produced through assimilation and fractional crystallization in which primary alkali basaltic and olivine tholeiitic melts 'erode' and assimilate the base of the crust. The increasingly tholeiitic character of the basalts towards the centre of Iceland, which reflects a higher degree of partial melting, is qualitatively consistent with increasing geothermal gradient and negative gravity anomaly. The highest Sr isotope ratio in Recent basalts from Iceland is observed inÖr˦fajökull volcano, which has a 3He/ 4He ratio ( R/Ra≈ 7.8) close to the MORB value, and this might represent a mantle source similar to that of Mauna Loa in Hawaii.

  18. Petrologic models of 15388, a unique Apollo 15 mare basalt

    NASA Technical Reports Server (NTRS)

    Hughes, S. S.; Dasch, E. J.; Nyquist, L. E.

    1993-01-01

    Mare basalt 15388, a feldspathic microgabbro from the Apennine Front, is chemically and petrographically distinct from Apollo 15 picritic, olivine-normative (ON), and quartz-normative basalts. The evolved chemistry, coarse texture, lack of olivine, and occurrence of cristobalite in 15388 argue for derivation by a late-stage magmatic process that is significantly removed from parental magma. It either crystallized from a magma evolved from the more mafic Apollo 15 basalts, or it crystallized from a currently unrepresented magma. Rb-Sr and Sm-Nd isotopic systematics yield isochron ages of 3.391 plus or minus 0.036 and 3.42 plus or minus 0.07 Ga, respectively, and epsilon(sub Nd) = 8.6 plus or minus 2.4, which is relatively high for Apollo 15 mare basalts. In contrast to chemical patterns of average Apollo 15 ON basalts and Apollo 15 picritic basalt, 15388 has a strongly positive LREE slope, high Ti, shallower HREE slope and a slightly positive Eu anomaly. These features argue against 15388 evolution by simple olivine fractionation of a parental ON or picritic basalt magma, although olivine is a dominant liquidus phase in both potential parents.

  19. Comparative Planetary Mineralogy: Valence State Partitioning of Cr, Fe, Ti, and V Among Crystallographic Sites in Olivine, Pyroxene, and Spinel from Planetary Basalts

    NASA Technical Reports Server (NTRS)

    Papike, J. J.; Karner, J. M.; Shearer, C. K.

    2005-01-01

    We have considered the valence-state partitioning of Cr, Fe, Ti, and V over crystallographic sites in olivine, pyroxene, and spinel from planetary basalts. The sites that accommodate these cations are the M2 site (6-8 coordinated) and M1 site (6 coordinated) in pyroxene, the M2 site (6-8 coordinated) and M1 site (6 coordinated) in olivine, and the tetrahedral and octahedral sites in spinel. The samples we studied are basalts from Earth, Moon, and Mars, which have fO2 conditions that range from IW-2 (Moon) to IW+6 (Earth) with Mars somewhere between at IW to IW+2. In this range of fO2 the significant elemental valences are (from low to high fO2) Ti4+, V3+, Fe2+, Cr2+, Cr3+, V3+, V4+, and Fe3+. V2+ and Ti3+ play a minor role in the phases considered for the Moon, and are probably in very low concentrations. V5+ plays a minor role in these phases in terrestrial basalts because it is probably in lower abundance than V4+ and it has an ionic radii that is so small (0.054 nm, 6- coordinated,[1]) that it is almost at the lower limit for octahedral coordination. The role of Cr2+ in the Moon is significant, as Sutton et al. [2] found that lunar olivine contains mostly Cr2+ while coexisting pyroxene contains mostly Cr3+. Hanson one vacancy only accommodates one V4+. Thus more vacancies are required in V4+ substitutions into olivine. In the Moon V3+ is much more abundant than V4+ [7, 8]. Thus in lunar chromite V3+ follows Cr3+, whereas in Earth V4+ (which is much greater in abundance than V3+) follows Ti4+ (eg in ulv spinel). We could go on in this vein for some time but space limitations do not permit us to do so.

  20. An Apollo 15 Mare Basalt Fragment and Lunar Mare Provinces

    NASA Technical Reports Server (NTRS)

    Ryder, Graham; Burling, Trina Cox

    1996-01-01

    Lunar sample 15474,4 is a tiny fragment of olivine-augite vitrophyre that is a mare basalt. Although petroraphically distinct from all other Apollo 15 samples, it has been ignored since its first brief description. Our new petrographic and mineral chemical data show that the olivines and pyroxenes are distinct from those in other basalts. The basalt cooled and solidified extremely rapidly; some of the olivine might be cumulate or crystallized prior to extrusion. Bulk-chemical data show that the sample is probably similar to an evolved Apollo 15 olivine-normative basalt in major elements but is distinct in its rare earth element pattern. Its chemical composition and petrography both show that 15474,4 cannot be derived from other Apollo 15 mare basalts by shallow-level crystal fractionation. It represents a distinct extrusion of magma. Nonetheless, the chemical features that 15474,4 has in common with other Apollo 15 mare basalts, including the high FeO/Sc, the general similarity of the rare earth element pattern, and the common (and chondritic) TiO2/Sm ratio, emphasize the concept of a geochemical province at the Apollo 15 site that is distinct from basalts and provinces elsewhere. In making a consistent picture for the derivation of all of the Apollo 15 basalts, both the commonalities and the differences among the basalts must be explained. The Apollo 15 commonalities and differences suggest that the sources must have consisted of major silicate phases with the same composition but with varied amounts of a magma trapped from a contemporary magma ocean. They probably had a high olivine/pyroxene ratio and underwent small and reasonably consistent degrees of partial melting to produce the basalts. These inferences may be inconsistent with models that suggest greatly different depths of melting among basalts, primitive sources for the green glasses, or extensive olivine fractionation during ascent. An integrated approach to lunar mare provinces, of which the Apollo 15

  1. Recycled Crust in the Mantle: Is High-Ni Olivine the Smoking Gun or a Red Herring?

    NASA Astrophysics Data System (ADS)

    Li, C.; Ripley, E. M.

    2008-12-01

    It is widely accepted that small amounts of recycled crustal components are present in some mantle-derived mafic and ultramafic magmas. This concept is supported by many isotopic and trace element studies of basalts, picrites and komatiites in the last 30 years. Recently Sobolev et al. [1,2] used olivine compositions such as Ni content and Mn/Fe ratio to demonstrate that the amounts of the recycled crustal component (i.e. pyroxenite) in these mantle-derived melts are much larger than previously appreciated. Their calculations show that the pyroxenite-derived component varies mostly between 40 and 80% for Hawaiian shield basalts and Siberian flood basalts, and mostly between 10 and 40% for mid-ocean ridge basalts and Archean komatiities. However, a critical test using olivine-liquid Mg-Fe equilibrium that was overlooked by Sobolev et al. [1,2] reveals that mixing of the two end-members (pyroxenite-derived and peridotite-derived melts) that were used in their models cannot generate the parental melts for the above natural samples. Such a discrepancy prompts us to reexamine the conventional view of a peridotite-dominant source for the Hawaiian shield basalts. This hypothesis has been criticized recently by many people because the contents of Ni in olivine phenocrysts in the basalts are significantly higher than mantle olivines in associated peridotite xenoliths and because total pressure has little effect on olivine-liquid Ni partition coefficient (DNi). What has not been generally considered is that the depth of olivine crystallization/equilibration has a negative effect on olivine Ni content because DNi is negatively correlated with melt temperature which decreases during adiabatic ascent. To evaluate such an effect quantitatively we have used all available experimental results of Ni partitioning between olivine and liquid to construct a robust empirical equation for DNi based on melt composition and temperature. The results of our calculations indicate that the

  2. Production of 21Ne in depth-profiled olivine from a 54 Ma basalt sequence, Eastern Highlands (37° S), Australia

    NASA Astrophysics Data System (ADS)

    Matchan, Erin L.; Honda, Masahiko; Barrows, Timothy T.; Phillips, David; Chivas, Allan R.; Fifield, L. Keith; Fabel, Derek

    2018-01-01

    In this study we investigate the cosmogenic neon component in olivine samples from a vertical profile in order to quantify muogenic 21Ne production in this mineral. Samples were collected from an 11 m thick Eocene basalt profile in the Eastern Highlands of southeastern Australia. An eruption age of 54.15 ± 0.36 Ma (2σ) was determined from 40Ar/39Ar step-heating experiments (n = 6) on three whole-rock samples. A 36Cl profile on the section indicated an apparent steady state erosion rate of 4.7 ± 0.5 m Ma-1. The eruption age was used to calculate in situ produced radiogenic 4He and nucleogenic 3He and 21Ne concentrations in olivine. Olivine mineral separates (n = 4), extracted from the upper two metres of the studied profile, reveal cosmogenic 21Ne concentrations that attenuate exponentially with depth. However, olivine (Fo68) extracted from below 2 m does not contain discernible 21Ne aside from magmatic and nucleogenic components, with the exception of one sample that apparently contained equal proportions of nucleogenic and muogenic neon. Modelling results suggest a muogenic neon sea-level high-latitude production rate of 0.02 ± 0.04 to 0.9 ± 1.3 atoms g-1 a-1 (1σ), or <2.5% of spallogenic cosmogenic 21Ne production at Earth's surface. These data support a key implicit assumption in the literature that accumulation of muogenic 21Ne in olivine in surface samples is likely to be negligible/minimal compared to spallogenic 21Ne.

  3. Phase relations of a simulated lunar basalt as a function of oxygen fugacity, and their bearing on the petrogenesis of the Apollo 11 basalts

    USGS Publications Warehouse

    Tuthill, R.L.; Sato, M.

    1970-01-01

    A glass of Apollo 11 basalt composition crystallizing at 1 atm at low f{hook}02 showed the following crystallization sequence; ferropseudobrookite at 1210??C, olivine at 1200??C, ilmenite and plagioclase at 1140??C, clinopyroxene at 1113??C. Ferropseudobrookite and olivine have a reaction relation to the melt. This sequence agrees with that assumed on textural grounds for some Apollo 11 basalts. It also indicates that the Apollo 11 basalts cannot have been modified by low-pressure fractionation. ?? 1970.

  4. Natural fumarolic alteration of fluorapatite, olivine, and basaltic glass, and implications for habitable environments on Mars.

    PubMed

    Hausrath, Elisabeth M; Tschauner, Oliver

    2013-11-01

    Fumaroles represent a very important potential habitat on Mars because they contain water and nutrients. Global deposition of volcanic sulfate aerosols may also have been an important soil-forming process affecting large areas of Mars. Here we identify alteration from the Senator fumarole, northwest Nevada, USA, and in low-temperature environments near the fumarole to help interpret fumarolic and acid vapor alteration of rocks and soils on Mars. We analyzed soil samples and fluorapatite, olivine, and basaltic glass placed at and near the fumarole in in situ mineral alteration experiments designed to measure weathering under natural field conditions. Using synchrotron X-ray diffraction, we clearly observe hydroxyl-carbonate-bearing fluorapatite as a fumarolic alteration product of the original material, fluorapatite. The composition of apatites as well as secondary phosphates has been previously used to infer magmatic conditions as well as fumarolic conditions on Mars. To our knowledge, the observations reported here represent the first documented instance of formation of hydroxyl-carbonate-bearing apatite from fluorapatite in a field experiment. Retreat of olivine surfaces, as well as abundant NH4-containing minerals, was also characteristic of fumarolic alteration. In contrast, alteration in the nearby low-temperature environment resulted in formation of large pits on olivine surfaces, which were clearly distinguishable from the fumarolic alteration. Raman signatures of some fumarolically impacted surfaces are consistent with detection of the biological molecules chlorophyll and scytenomin, potentially useful biosignatures. Observations of altered minerals on Mars may therefore help identify the environment of formation and understand the aqueous history and potential habitability of that planet.

  5. Extraction of in situ cosmogenic 14C from olivine

    USGS Publications Warehouse

    Pigati, J.S.; Lifton, N.A.; Timothy, Jull A.J.; Quade, Jay

    2010-01-01

    Chemical pretreatment and extraction techniques have been developed previously to extract in situ cosmogenic radiocarbon (in situ 14C) from quartz and carbonate. These minerals can be found in most environments on Earth, but are usually absent from mafic terrains. To fill this gap, we conducted numerous experiments aimed at extracting in situ 14C from olivine ((Fe,Mg)2SiO4). We were able to extract a stable and reproducible in situ 14C component from olivine using stepped heating and a lithium metaborate (LiBO2) flux, following treatment with dilute HNO3 over a variety of experimental conditions. However, measured concentrations for samples from the Tabernacle Hill basalt flow (17.3 ?? 0.3 ka4) in central Utah and the McCarty's basalt flow (3.0 ?? 0.2 ka) in western New Mexico were significantly lower than expected based on exposure of olivine in our samples to cosmic rays at each site. The source of the discrepancy is not clear. We speculate that in situ 14C atoms may not have been released from Mg-rich crystal lattices (the olivine composition at both sites was ~Fo65Fa35). Alternatively, a portion of the 14C atoms released from the olivine grains may have become trapped in synthetic spinel-like minerals that were created in the olivine-flux mixture during the extraction process, or were simply retained in the mixture itself. Regardless, the magnitude of the discrepancy appears to be inversely proportional to the Fe/(Fe+Mg) ratio of the olivine separates. If we apply a simple correction factor based on the chemical composition of the separates, then corrected in situ 14C concentrations are similar to theoretical values at both sites. At this time, we do not know if this agreement is fortuitous or real. Future research should include measurement of in situ 14C concentrations in olivine from known-age basalt flows with different chemical compositions (i.e. more Fe-rich) to determine if this correction is robust for all olivine-bearing rocks. ?? 2010 by the Arizona

  6. Effect of Sulfur on Siderophile Element Partitioning Between Olivine and Martian Primary Melt

    NASA Technical Reports Server (NTRS)

    Usui, T.; Shearer, C. K.; Righter, K.; Jones, J. H.

    2011-01-01

    Since olivine is a common early crystallizing phase in basaltic magmas that have produced planetary and asteroidal crusts, a number of experimental studies have investigated elemental partitioning between olivine and silicate melt [e.g., 1, 2, 3]. In particular, olivine/melt partition coefficients of Ni and Co (DNi and DCo) have been intensively studied because these elements are preferentially partitioned into olivine and thus provide a uniquely useful insight into the basalt petrogenesis [e.g., 4, 5]. However, none of these experimental studies are consistent with incompatible signatures of Co [e.g., 6, 7, 8] and Ni [7] in olivines from Martian meteorites. Chemical analyses of undegassed MORB samples suggest that S dissolved in silicate melts can reduce DNi up to 50 % compared to S-free experimental systems [9]. High S solubility (up to 4000 ppm) for primitive shergottite melts [10] implies that S might have significantly influenced the Ni and Co partitioning into shergottite olivines. This study conducts melting experiments on Martian magmatic conditions to investigate the effect of S on the partitioning of siderophile elements between olivine and Martian primary melt.

  7. Basalt generation at the Apollo 12 site. Part 1: New data, classification, and re-evaluation

    NASA Technical Reports Server (NTRS)

    Neal, Clive R.; Hacker, Matthew D.; Snyder, Gregory A.; Taylor, Lawrence A.; Liu, Yun-Gang; Schmitt, Roman A.

    1994-01-01

    New data are reported from five previously unanalyzed Apollo 12 mare basalts that are incorporated into an evaluation of previous petrogenetic models and classification schemes for these basalts. This paper proposes a classification for Apollo 12 mare basalts on the basis of whole-rock Mg# (molar 100*(Mg/(Mg+Fe))) and Rb/Sr ratio (analyzed by isotope dilution), whereby the ilmenite, olivine, and pigeonite basalt groups are readily distinguished from each other. Scrutiny of the Apollo 12 feldspathic 'suite' demonstrates that two of the three basalts previously assigned to this group (12031, 12038, 12072) can be reclassified: 12031 is a plagioclase-rich pigeonite basalt; and 12072 is an olivine basalt. Only basalt 12038 stands out as a unique sample to the Apollo 12 site, but whether this represents a single sample from another flow at the Apollo 12 site or is exotic to this site is equivocal. The question of whether the olivine and pigeonite basalt suites are co-magmatic is addressed by incompatible trace-element chemistry: the trends defined by these two suites when Co/Sm and Sm/Eu ratios are plotted against Rb/Sr ratio demonstrate that these two basaltic types cannot be co-magmatic. Crystal fractionation/accumulation paths have been calculated and show that neither the pigeonite, olivine, or ilmenite basalts are related by this process. Each suite requires a distinct and separate source region. This study also examines sample heterogeneity and the degree to which whole-rock analyses are representative, which is critical when petrogenetic interpretation is undertaken. Sample heterogeneity has been investigated petrographically (inhomogeneous mineral distribution) with consideration of duplicate analyses, and whether a specific sample (using average data) plots consistently upon a fractionation trend when a number of different compostional parameters are considered. Using these criteria, four basalts have been identified where reported analyses are not

  8. Comparative Planetary Mineralogy: Basaltic Plagioclase from Earth, Moon, Mars and 4 Vesta

    NASA Technical Reports Server (NTRS)

    Karner, J. M.; Papike, J. J.; Shearer, C. K.

    2003-01-01

    Major, minor and trace element analysis of silicates has allowed for the study of planetary basalts in a comparative planetary mineralogy context. We continue this initiative by exploring the chemistry of plagioclase feldspar in basalts from the Earth, Moon, Mars and 4 Vesta. This paper presents new data on plagioclase from six terrestrial basalt suites including Keweenawan, Island Arc, Hawaiian, Columbia Plateau, Taos Plateau, and Ocean Floor; six lunar basalt suites including Apollo 11 Low K, Apollo 12 Ilmenite, Apollo 12 Olivine, Apollo 12 Pigeonite, Apollo 15 Olivine, and Apollo 15 Pigeonite; two basaltic martian meteorites, Shergotty and QUE 94201; and one unequilibrated eucrite, Pasamonte.

  9. Flow in the shallow mantle in the westernmost Mediterranean: insights from xenoliths in Plio-Pleistocene alkali basalts from the eastern Betic Cordillera (SE Spain)

    NASA Astrophysics Data System (ADS)

    Konc, Zoltán; Hidas, Károly; Garrido, Carlos J.; Tommasi, Andréa; Vauchez, Alain; Padrón Navarta, José Alberto; Marchesi, Claudio; Acosta-Vigil, Antonio; Szabó, Csaba; Varas-Reus, Maria Isabel

    2016-04-01

    Peridotite mantle xenoliths in Plio-Pleistocene alkali basalts of the eastern Betic Cordillera (Cartagena area, Murcia, SE Spain) provide a snapshot of the structure and composition of the lithospheric mantle at the northern limb of the Alpine Betic-Rif arched belt in the westernmost Mediterranean. The xenoliths are spinel and plagioclase lherzolite with minor harzburgite and wehrlite, displaying porphyroclastic to equigranular textures. Regardless of composition and texture, the Crystal Preferred Orientation (CPO) of olivine shows an axial-[100] pattern characterized by a strong alignment of [100]-axes near or parallel to the peridotite lineation and a girdle distribution of [010]-axes with a maximum normal to the peridotite foliation. This CPO pattern is consistent with ductile deformation accommodated by dislocation creep with dominant activation of the high temperature {0kl}[100] olivine slip system, indicative of deformation by simple shear or combinations of simple shear and pure shear with a transtensional component. Calculated seismic properties are characterized by fast propagation of P-waves and polarization of fast S-waves parallel to olivine [100]-axis, indicating the flow direction. SKS and Pn anisotropy in the eastern Betics can be explained by a lithospheric mantle peridotite with similar fabric to the one displayed by the studied mantle xenoliths. Considering the limited thickness of the mantle lithosphere in the Betics (40-80 km), the measured azimuths and delays of SKS waves in the eastern Betics are consistent with a steeply dipping mantle foliation and a subhorizontal lineation with ENE strike. This geometry of the lithospheric fabrics implies active or frozen mantle flow with a dominantly strike-slip component subparallel to the paleo-Iberian margin. Synkinematic overprinting of mineral assemblages from the garnet-spinel to the plagioclase facies demonstrates 36-40 km uplift continuously accommodated by ductile shear thinning of the

  10. Natural Fumarolic Alteration of Fluorapatite, Olivine, and Basaltic Glass, and Implications for Habitable Environments on Mars

    PubMed Central

    Tschauner, Oliver

    2013-01-01

    Abstract Fumaroles represent a very important potential habitat on Mars because they contain water and nutrients. Global deposition of volcanic sulfate aerosols may also have been an important soil-forming process affecting large areas of Mars. Here we identify alteration from the Senator fumarole, northwest Nevada, USA, and in low-temperature environments near the fumarole to help interpret fumarolic and acid vapor alteration of rocks and soils on Mars. We analyzed soil samples and fluorapatite, olivine, and basaltic glass placed at and near the fumarole in in situ mineral alteration experiments designed to measure weathering under natural field conditions. Using synchrotron X-ray diffraction, we clearly observe hydroxyl-carbonate-bearing fluorapatite as a fumarolic alteration product of the original material, fluorapatite. The composition of apatites as well as secondary phosphates has been previously used to infer magmatic conditions as well as fumarolic conditions on Mars. To our knowledge, the observations reported here represent the first documented instance of formation of hydroxyl-carbonate-bearing apatite from fluorapatite in a field experiment. Retreat of olivine surfaces, as well as abundant NH4-containing minerals, was also characteristic of fumarolic alteration. In contrast, alteration in the nearby low-temperature environment resulted in formation of large pits on olivine surfaces, which were clearly distinguishable from the fumarolic alteration. Raman signatures of some fumarolically impacted surfaces are consistent with detection of the biological molecules chlorophyll and scytenomin, potentially useful biosignatures. Observations of altered minerals on Mars may therefore help identify the environment of formation and understand the aqueous history and potential habitability of that planet. Key Words: Fumaroles—Mars—Olivine—Acidophile—Geothermal—Search for life (biosignatures)—Synchrotron X-ray diffraction. Astrobiology 13, 1049–1064

  11. Basaltic Soil of Gale Crater: Crystalline Component Compared to Martian Basalts and Meteorites

    NASA Technical Reports Server (NTRS)

    Treiman, A. H.; Bish, D. L.; Ming, D. W.; Morris, R. V.; Schmidt, M.; Downs, R. T.; Stolper, E. M.; Blake, D. F.; Vaniman, D. T.; Achilles, C. N.; hide

    2013-01-01

    A significant portion of the soil of the Rocknest dune is crystalline and is consistent with derivation from unweathered basalt. Minerals and their compositions are identified by X-ray diffraction (XRD) data from the CheMin instrument on MSL Curiosity. Basalt minerals in the soil include plagioclase, olivine, low- and high-calcium pyroxenes, magnetite, ilmenite, and quartz. The only minerals unlikely to have formed in an unaltered basalt are hematite and anhydrite. The mineral proportions and compositions of the Rocknest soil are nearly identical to those of the Adirondack-class basalts of Gusev Crater, Mars, inferred from their bulk composition as analyzed by the MER Spirit rover.

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

    NASA Technical Reports Server (NTRS)

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

    2014-01-01

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

  13. Submarine basalt from the Revillagigedo Islands region, Mexico

    USGS Publications Warehouse

    Moore, J.G.

    1970-01-01

    Ocean-floor dredging and submarine photography in the Revillagigedo region off the west coast of Mexico reveal that the dominant exposed rock of the submarine part of the large island-forming volcanoes (Roca Partida and San Benedicto) is a uniform alkali pillow basalt; more siliceous rocks are exposed on the upper, subaerial parts of the volcanoes. Basalts dredged from smaller seamounts along the Clarion fracture zone south of the Revillagigedo Islands are tholeiitic pillow basalts. Pillows of alkali basalts are more vesicular than Hawaiian tholeiitic pillows collected from the same depths. This difference probably reflects a higher original volatile content of the alkali basalts. Manganese-iron oxide nodules common in several dredge hauls generally contain nucleii of rhyolitic pumice or basalt pillow fragments. The pumice floated to its present site from subaerial eruptions, became waterlogged and sank, and was then coated with manganese-iron oxides. The thickness of palagonite rinds on the glassy pillow fragments is proportional to the thickness of manganese-iron oxide layers, and both are a measure of the age of the nodule. Both oldest basalts (10-100 m.y.) and youngest (less than 1 m.y.) are along the Clarion fracture zone, whereas basalts from Roca Partida and San Benedicto volcanoes are of intermediate age. ?? 1970.

  14. New Insights to the Mid Miocene Calc-alkaline Lavas of the Strawberry Volcanics, NE Oregon Surrounded by the Coeval Tholeiitic Columbia River Basalt Province

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

    The Strawberry Volcanics (SV) of NE Oregon were distributed over 3,400 km2 during the mid-Miocene and comprise a diverse volcanic suite, which span the range of compositions from basalt to rhyolite. The predominant composition of this volcanic suite is calc-alkaline (CA) basaltic andesite and andesite, although tholeiitic (TH) lavas of basalt to andesite occur as well. The coeval flood basalts of the Columbia River province surround the SV. Here we will discuss new ages and geochemical data, and present a new geologic map and stratigraphy of the SV. The SV are emplaced on top of pre-Tertiary accreted terranes of the Blue Mountain Province, Mesozoic plutonic rocks, and older Tertiary volcanic rocks thought to be mostly Oligocene of age. Massive rhyolites (~300 m thick) are exposed mainly along the western flank and underlie the intermediate composition lavas. In the southern portion of this study area, alkali basaltic lavas, thought to be late Miocene to early Pliocene in age, erupted and overlie the SV. In addition, several regional ignimbrites reach into the area. The 9.7 Ma Devine Canyon Tuff and the 7.1 Ma Rattlesnake Tuff also overlie the SV. The 15.9-15.4 Ma Dinner Creek Tuff is mid-Miocene, and clear stratigraphic relationships are found in areas where the tuff is intercalated between thick SV lava flows. All of the basalts of the SV are TH and are dominated by phenocryst-poor (≤2%) lithologies. These basalts have an ophitic texture dominated by plagioclase, clinopyroxene and olivine (often weathered to iddingsite). Basalts and basaltic andesites have olivine Fo #'s ranging from 44 at the rims (where weathered to iddingsite) and as high as 88 at cores. Pyroxene Mg #'s range from 65 to 85. Andesites of the SV are sub-alkaline, and like the basalts, are exceedingly phenocryst-poor (≤3%) with microphenocrysts of plagioclase and lesser pyroxene and olivine, which occasionally occur as crystal clots of ~1-3 mm instead of single crystals. In addition, minimal

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

    NASA Astrophysics Data System (ADS)

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

    2017-11-01

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

  16. The Plumbing System of a Highly Explosive Basaltic Volcano: Sunset Crater, AZ

    NASA Astrophysics Data System (ADS)

    Allison, C. M.; Roggensack, K.; Clarke, A. B.

    2015-12-01

    We seek to better understand highly explosive basaltic eruptions with specific focus on magmatic volatile solubility in alkali basalts and the magma plumbing system. Sunset Crater, an alkali basalt (~3.7 wt.% alkalis) scoria cone volcano, erupted explosively in 1085 AD. We analyzed 125 primary melt inclusions (MIs) from Sunset Crater tephra deposited by 2 subplinian phases and 1 Strombolian explosion to compare magma volatiles and storage conditions. We picked rapidly quenched free olivine crystals and selected large volume MIs (50-180 μm) located toward crystal cores. MIs are faceted and exhibit little major element composition variability with minor post entrapment crystallization (2-10%). MIs are relatively dry but CO2-rich. Water content varies from 0.4 wt.% to 1.5 wt.% while carbon dioxide abundance ranges between 1,150 ppm and 3,250 ppm. Most MIs contain >1 wt.% H2O and >2,150 ppm CO2. All observed MIs contain a vapor bubble, so we are evaluating MI vapor bubbles with Raman spectroscopy and re-homogenization experiments to determine the full volatile budget. Because knowledge of volatile solubility is critical to accurately interpret results from MI analyses, we measured H2O-CO2 solubility in the Sunset Crater bulk composition. Fluid-saturated experiments at 4 and 6 kbar indicate shallower entrapment pressures for these MIs than values calculated for this composition using existing models. Assuming fluid saturation, MIs record depths from 6 km to 14 km, including groupings suggesting two pauses for longer-term storage at ~6 km and ~10.5 km. We do not observe any significant differences in MIs from phases exhibiting different eruptive styles, suggesting that while a high CO2 content may drive rapid magma ascent and be partly responsible for highly explosive eruptions, shallower processes may govern the final eruptive character. To track shallow processes during magma ascent from depth of MI-entrapment up to the surface, we are examining MI re-entrants.

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

    NASA Astrophysics Data System (ADS)

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

    2017-04-01

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

  18. The consanguinity of the oldest Apollo 11 mare basalts

    NASA Technical Reports Server (NTRS)

    Gamble, R. P.; Coish, R. A.; Taylor, L. A.

    1978-01-01

    The textural, mineralogical, and chemical relationships between three of the oldest dates lunar mare basalt samples returned by Apollo 11 (10003, 10029 and 10062) were investigated. Very strong resemblances were noted between the modal minerologies of 10003 and 10029. Significantly more modal olivine and cristobalite was observed in 10062 than in the other basalt samples. A detailed examination of mineral-chemical relationships among the samples revealed similarities between 10003 and 10062 and differences between these two rocks and 10029, the most significant of which is the presence of akaganeite in 10029, implying that lawrencite was present in the pristine sample of 10029 but not in 10003 and 10062. Results of a Wright-Doherty mixing program used to test various fractional crystallization schemes show that 10062 can be derived from a liquid with the composition of either 10003 or 10029 by removing 2-5% ilmenite and 5% olivine. By removing about 6% plagioclase, 10003 can be derived from a liquid with the bulk composition of 10062. It is concluded that 10003 and 10029 may have come from different basaltic flows, whereas it is possible that 10003 and 10062 were derived from the same parental magma by near-surface fractionation of olivine plus ilmenite or of plagioclase plus or minus olivine.

  19. Very high potassium (VHK) basalt - Complications in mare basalt petrogenesis

    NASA Technical Reports Server (NTRS)

    Shervais, J. W.; Taylor, L. A.; Laul, J. C.; Shih, C.-Y.; Nyquist, L. E.

    1985-01-01

    The first comprehensive report on the petrology and geochemistry of Apollo 14 VHK (Very High Potassium) basalts and their implications for lunar evolution is presented. The reported data are most consistent with the hypothesis that VHK basalts formed through the partial assimilation of granite by a normal low-Ti, high-Al mare basalt magma. Assimilation was preceded by the diffusion-controlled exchange of alkalis and Ba between basalt magma and the low-temperature melt fraction of the granite. Hypotheses involving volatile/nonvolatile fractionations or long-term enrichment of the source regions in K are inconsistent with the suprachondritic Ba/La ratios and low initial Sr-87/Sr-86 ratios of VHK basalt. An important implication of this conclusion is that granite should be a significant component of the lunar crust at the Apollo 14 site.

  20. Clinopyroxene dissolution in basaltic melt

    NASA Astrophysics Data System (ADS)

    Chen, Yang; Zhang, Youxue

    2009-10-01

    The history of magmatic systems may be inferred from reactions between mantle xenoliths and host basalt if the thermodynamics and kinetics of the reactions are quantified. To study diffusive and convective clinopyroxene dissolution in silicate melts, diffusive clinopyroxene dissolution experiments were conducted at 0.47-1.90 GPa and 1509-1790 K in a piston-cylinder apparatus. Clinopyroxene saturation is found to be roughly determined by MgO and CaO content. The effective binary diffusivities, DMgO and DCaO, and the interface melt saturation condition, C0MgO×C0CaO, are extracted from the experiments. DMgO and DCaO show Arrhenian dependence on temperature. The pressure dependence is small and not resolved within 0.47-1.90 GPa. C0MgO×C0CaO in the interface melt increases with increasing temperature, but decreases with increasing pressure. Convective clinopyroxene dissolution, where the convection is driven by the density difference between the crystal and melt, is modeled using the diffusivities and interface melt saturation condition. Previous studies showed that the convective dissolution rate depends on the thermodynamics, kinetics and fluid dynamics of the system. Comparing our results for clinopyroxene dissolution to results from a previous study on convective olivine dissolution shows that the kinetic and fluid dynamic aspects of the two minerals are quite similar. However, the thermodynamics of clinopyroxene dissolution depends more strongly on the degree of superheating and composition of the host melt than that of olivine dissolution. The models for clinopyroxene and olivine dissolution are tested against literature experiments on mineral-melt interaction. They are then applied to previously proposed reactions between Hawaii basalts and mantle minerals, mid-ocean ridge basalts and mantle minerals, and xenoliths digestion in a basalt at Kuandian, Northeast China.

  1. Basalt generation at the Apollo 12 site. Part 2: Source heterogeneity, multiple melts, and crustal contamination

    NASA Technical Reports Server (NTRS)

    Neal, Clive R.; Hacker, Matthew D.; Snyder, Gregory A.; Taylor, Lawrence A.; Liu, Yun-Gang; Schmitt, Roman A.

    1994-01-01

    The petrogenesis of Apollo 12 mare basalts has been examined with emphasis on trace-element ratios and abundances. Vitrophyric basalts were used as parental compositions for the modeling, and proportions of fractionating phases were determined using the MAGFOX prograqm of Longhi (1991). Crystal fractionation processes within crustal and sub-crustal magma chambers are evaluated as a function of pressure. Knowledge of the fractionating phases allows trace-element variations to be considered as either source related or as a product of post-magma-generation processes. For the ilmenite and olivine basalts, trace-element variations are inherited from the source, but the pigeonite basalt data have been interpreted with open-system evolution processes through crustal assimilation. Three groups of basalts have been examined: (1) Pigeonite basalts-produced by the assimilation of lunar crustal material by a parental melt (up to 3% assimilation and 10% crystal fractionation, with an 'r' value of 0.3). (2) Ilmenite basalts-produced by variable degrees of partial melting (4-8%) of a source of olivine, pigeonite, augite, and plagioclase, brought together by overturn of the Lunar Magma Ocean (LMO) cumulate pile. After generation, which did not exhaust any of the minerals in the source, these melts experienced closed-system crystal fractionation/accumulation. (3) Olivine basalts-produced by variable degrees of partial melting (5-10%) of a source of olivine, pigeonite, and augite. After generation, again without exhausting any of the minerals in the source, these melts evolved through crystal accumulation. The evolved liquid counterparts of these cumulates have not been sampled. The source compositions for the ilmenite and olivine basalts were calculated by assuming that the vitrophyric compositions were primary and the magmas were produced by non-modal batch melting. Although the magnitude is unclear, evaluation of these source regions indicates that both be composed of early- and

  2. Laboratory Simulated Acid-Sulfate Weathering of Basaltic Materials: Implications for Formation of Sulfates at Meridiani Planum and Gusev Crater, Mars

    NASA Technical Reports Server (NTRS)

    Golden, D. C.; Ming, Douglas W.; Morris, Richard V.; Mertzman, A.

    2006-01-01

    Acid-sulfate weathering of basaltic materials is a candidate formation process for the sulfate-rich outcrops and rocks at the MER rover Opportunity and Spirit landing sites. To determine the style of acid-sulfate weathering on Mars, we weathered basaltic materials (olivine-rich glassy basaltic sand and plagioclase feldspar-rich basaltic tephra) in the laboratory under different oxidative, acid-sulfate conditions and characterized the alteration products. We investigated alteration by (1) sulfuric-acid vapor (acid fog), (2) three-step hydrothermal leaching treatment approximating an open system and (3) single-step hydrothermal batch treatment approximating a "closed system." In acid fog experiments, Al, Fe, and Ca sulfates and amorphous silica formed from plagioclase-rich tephra, and Mg and Ca sulfates and amorphous silica formed from the olivine-rich sands. In three-step leaching experiments, only amorphous Si formed from the plagioclase-rich basaltic tephra, and jarosite, Mg and Ca sulfates and amorphous silica formed from olivine-rich basaltic sand. Amorphous silica formed under single-step experiments for both starting materials. Based upon our experiments, jarosite formation in Meridiani outcrop is potential evidence for an open system acid-sulfate weathering regime. Waters rich in sulfuric acid percolated through basaltic sediment, dissolving basaltic phases (e.g., olivine) and forming jarosite, other sulfates, and iron oxides. Aqueous alteration of outcrops and rocks on the West Spur of the Columbia Hills may have occurred when vapors rich in SO2 from volcanic sources reacted with basaltic materials. Soluble ions from the host rock (e.g., olivine) reacted with S to form Ca-, Mg-, and other sulfates along with iron oxides and oxyhydroxides.

  3. Mare basalt magma source region and mare basalt magma genesis

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

    Binder, A.B.

    1982-11-15

    Given the available data, we find that the wide range of mare basaltic material characteristics can be explained by a model in which: (1) The mare basalt magma source region lies between the crust-mantle boundary and a maximum depth of 200 km and consists of a relatively uniform peridotite containing 73--80% olivine, 11--14% pyroxene, 4--8% plagioclase, 0.2--9% ilmenite and 1--1.5% chromite. (2) The source region consists of two or more density-graded rhythmic bands, whose compositions grade from that of the very low TiO/sub 2/ magma source regions (0.2% ilmenite) to that of the very high TiO/sub 2/ magma source regionsmore » (9% ilmenite). These density-graded bands are proposed to have formed as co-crystallizing olivine, pyroxene, plagioclase, ilmenite, and chromite settled out of a convecting magma (which was also parental to the crust) in which these crystals were suspended. Since the settling rates of the different minerals were governed by Stoke's law, the heavier minerals settled out more rapidly and therefore earlier than the lighter minerals. Thus the crystal assemblages deposited nearest the descending side of each convection cell were enriched in heavy ilmenite and chromite with respect to lighter olivine and pyroxene and very much lighter plagioclase. The reverse being the case for those units deposited near the ascending sides of the convection cells.« less

  4. Mineralogy of young lunar mare basalts: Assessment of temporal and spatial heterogeneity using M3 data from Chandrayaan-1

    NASA Astrophysics Data System (ADS)

    Varatharajan, Indhu; Srivastava, Neeraj; Murty, Sripada V. S.

    2014-07-01

    A comparative assessment of the mineralogy of young basalts (∼1.2 Ga to ∼2.8 Ga) from the western nearside, Moscoviense basin, and the Orientale basin of the Moon has been made using Level 2 Moon Mineralogy Mapper (M3) data from the Chandrayaan-1 mission. Spectral data characteristics of the individual units have been generated from fresh small craters to minimize the complications due to space weathering. Representative spectra for individual units and the derived spectral parameters (band centers and integrated band depth ratio) have been used to study composition of these young basalts. A modified approach of Gaffey et al. (Gaffey, M.J., Cloutis, E.A., Kelley, M.S., Reed, K.L. [2002]. Mineralogy of asteroids. In: Asteroids III. The University of Arizona Press, Tucson, pp. 183-204) (for olivine-pyroxene mixtures) and the methodology of Adams (Adams, J.B. [1974]. J. Geophys. Res. 79, 4829-4836. http://dx.doi.org/10.1029/JB079i032p04829) (for interpreting pyroxene type) have been used to improve our understanding of the spectral behavior of these basalts. Most of the young basalts of Oceanus Procellarum are characterized by abundant olivines and they show complex volcanic history. Vast exposures of olivine concentrated units having higher abundance of olivine content than high-Ca pyroxenes are emplaced in the northern Oceanus Procellarum region. Mostly, they show distinct stratigraphic gradation with the immediately underlying units of relatively lower olivine content. The Moscoviense unit shows signatures of Fe-rich glasses along with clinopyroxenes. The basalts of Orientale basin are typically devoid of olivine and are rich in high-Ca pyroxene. Thus, mineralogy of these mare basalts which erupted during the late stage volcanism vary across the Moon’s surface; however, broader observations reveal apparently higher FeO content in the younger basalts of western nearside and Orientale region.

  5. Petrology of dune sand derived from basalt on the Ka'u Desert, Hawaii

    NASA Technical Reports Server (NTRS)

    Gooding, J. L.

    1982-01-01

    Dune sand from the Ka'u Desert, southwest flank of Kilauea volcano, Hawaii, is moderately well-sorted (median = 1.60 Phi, deviation = 0.60, skewness = 0.25, kurtosis = 0.68) and composed mostly of frosted subangular particles of basalt glass ('unfractionated' olivine-normative tholeitte), olivine, lithic fragments (subophitic and intersertal basalts; magnetite-ilmenite-rich basalts), reticular basalt glass, magnetite, ilmenite, and plagioclase, in approximately that order of abundance. Quantitative lithological comparison of the dune sand with sand-sized ash from the Keanakakoi Formation supports suggestions that the dune sand was derived largely from Keanakakoi ash. The dune sand is too well sorted to have been emplaced in its present form by base-surge but could have evolved by post-eruption reworking of the ash.

  6. Carbon storage potential of Columbia River flood basalt

    NASA Astrophysics Data System (ADS)

    Wells, R. K.; Xiong, W.; Giammar, D.; Skemer, P. A.

    2017-12-01

    Basalt reservoirs are an important option for sequestering carbon through dissolution of host rock and precipitation of stable carbonate minerals. This study seeks to understand the nature of dissolution and surface roughening processes and their influence on the timing and spatial distribution of carbonation, in static experiments at 150 °C and 100 bar CO2. Intact samples and cores with milled pathways from Ca-rich and Fe-rich Columbia River flood basalt formations were reacted for up to 40 weeks. Experimental specimens were analyzed using SEM-EDS, microprobe, and μCT scanning, Raman spectroscopy, and 2D profilometer to characterize changes in composition and surface roughness. ICP-MS was used to examine bulk fluid chemistry. Initial dissolution of olivine grains results in higher Mg2+ and Fe2+ concentrations within the bulk solution in the first week of reaction. However, once available olivine grains are gone, Ca-rich pyroxene becomes the primary contributor of Ca2+, Mg2+, and Fe2+ within the bulk solution. The complete dissolution of olivine grains resulted in pits up to 200 μm deep. Dissolution of other minerals resulted in the formation of microscale textures, primarily along grain boundaries and fractures. The surface roughness increased by factors of up to 42, while surface area increased 20%. Based on these results, pyroxene is the sustaining contributor of divalent metal cations during dissolution of basalt, and the limited connectivity of olivine and pyroxene grains limits the exposure of new reactive surface areas. Within 6 weeks, aragonite precipitated in Ca-rich basalt samples, while Fe-rich samples precipitated of siderite. The highest concentration of carbonates occurs 1/3 into milled pathways, which simulate dead-end fractures, in low porosity basalts, and near the fracture tip in high porosity basalts. Even at elevated temperatures, the fractures are not blocked nor filled within 40 weeks of reaction. When vesicles are present, carbonates can

  7. Dissolution-precipitation reactions and permeability evolution from reactions of CO2-rich aqueous solutions with fractured basalt

    NASA Astrophysics Data System (ADS)

    Wells, R. K.; Xiong, W.; Bae, Y.; Sesti, E.; Skemer, P. A.; Giammar, D.; Conradi, M.; Ellis, B. R.; Hayes, S. E.

    2015-12-01

    The injection of CO2 into fractured basalts is one of several possible solutions to mitigate global climate change; however, research on carbonation in natural basalts in relation to carbon sequestration is limited, which impedes our understanding of the processes that may influence the viability of this strategy. We are conducting bench-scale experiments to characterize the mineral dissolution and precipitation and the evolution of permeability in synthetic and natural basalts exposed to CO2-rich fluids. Analytical methods include optical and electron microscopy, electron microprobe, Raman spectroscopy, nuclear magnetic resonance (NMR), and micro X-ray computed tomography (μCT) with variable flow rates. Reactive rock and mineral samples consist of 1) packed powders of olivine or natural basalt, and 2) sintered cores of olivine or a synthetic basalt mixture. Each sample was reacted in a batch reactor at 100 °C, and 100 bars CO2. Magnesite is detected within one day in olivine packed beds, and within 15 days in olivine sintered cores. Forsterite and synthetic basalt sinters were also reacted in an NMR apparatus at 102 °C and 65 bars CO2. Carbonate signatures are observed within 72 days of reaction. Longer reaction times are needed for carbonate precipitation in natural basalt samples. Cores from the Columbia River flood basalt flows that contain Mg-rich olivine and a serpentinized basalt from Colorado were cut lengthwise, the interface mechanically roughened or milled, and edges sealed with epoxy to simulate a fractured interface. The cores were reacted in a batch reactor at 50-150 °C and 100 bars CO2. At lower temperatures, calcite precipitation is rare within the fracture after 4 weeks. At higher temperatures, numerous calcite and aragonite crystals are observed within 1 mm of the fracture entrance along the roughened fracture surface. In flow-through experiments, permeability decreased along the fracture paths within a few hours to several days of flow.

  8. Bacterial Oxidation of Iron in Olivine: Implications for the Subsurface Biosphere, Global Chemical Cycles, and Life on Mars

    NASA Astrophysics Data System (ADS)

    Fisk, M. R.; Popa, R.; Smith, A. R.; Popa, R.; Boone, J.

    2011-12-01

    We isolated 21 species of bacteria from subseafloor and terrestrial basalt environments and which thrive on olivine at neutral pH. Cell numbers increase four to five orders of magnitude over three weeks in media where the only metabolic energy comes from the oxidation of Fe(II) in olivine. The subseafloor bacteria were isolated from a borehole on the flank of Juan de Fuca Ridge in the northeast Pacific basin where the temperature ranged from 4 up to 64 °C over four years. Terrestrial isolates originated from the basalt-ice boundary in a lava tube on the flank of Newberry Caldera in the Cascades of Oregon. The borehole water was either seawater or seawater plus subseafloor formation water and the lava tube ice was frozen meteoric or ground water. Although microorganisms capable of oxidizing iron for growth are known, microbes that oxidize iron from silicate minerals at neutral pH have not previously been cultured. The 21 species in this study are the first neutrophilic, iron-oxidizing bacteria (nFeOB) to be isolated and cultured that grow on olivine. These nFeOB are primary producers and we believe that they are a widespread component of the subsurface biosphere. In addition to their ability use iron from olivine, these microbes assimilate carbon from bicarbonate in solution and can grow when oxygen pressures are low. They also use nitrate as an alternative electron acceptor to oxygen in anaerobiosis. Since basalt is the most common rock in the Earth's crust and iron is the fourth most abundant element in the crust, we believe nFeOB are likely to be a significant portion of the subsurface biosphere. They are likely to affect, and perhaps in some environments control, the weathering rate of olivine and possibly of pyroxene and basalt glass. Olivine is a component of Mars's surface and it is present on other rocky bodies in the solar system. The ability of these bacteria to use Fe(II) from olivine, to assimilate carbon, to grow at low temperature, and to use low

  9. Thermobarometry for spinel lherzolite xenoliths in alkali basalts

    NASA Astrophysics Data System (ADS)

    Ozawa, Kazuhito; Youbi, Nasrrddine; Boumehdi, Moulay Ahmed; Nagahara, Hiroko

    2016-04-01

    geothermobarometry based on reactions with large and distinct volume changes, is necessary. Specification of mineral domains and their components representing the thermal state of the mantle just before xenolith extraction is one of the major tasks for the establishment of reliable geothermobarometry for spinel lherzolite xenoliths. Systematic variations of such mineralogical information among xenoliths transported by a single volcanic eruption guarantees proper estimation of a mantle geotherm. For the development of such geobarometry, it is important to choose appropriate xenolith locality, where previous studies provide enough information and where many xenolith samples are available for extending a range of derivation depth. Spinel lherzolite xenoliths in alkali basalts from Bou Ibalhatene maars in the Middle Atlas in Morocco are suitable study target. Geochemical, geochronological, petrological, and rheological aspects of the spinel lherzolite xenoliths have been studied (Raffone et al. 2009; El Messbahi et al., 2015; Witting et al., 2010; El Azzouzi et al., 2010), which show that they represent fragments of the lithospheric mantle formed and modified since 1.7Ga before their extraction from Miocene to recent. We have pinpointed portions of minerals in the xenolith samples and their components representing condition just before their entrapment in magmas, on which appropriate geothermobarometers are applied and detected ~0.5GPa pressure difference (1.5-2.0GPa) for ~100°C variation in temperatures (950-1050°C).

  10. Plagioclase mineralogy of olivine alkaline basalt

    NASA Technical Reports Server (NTRS)

    Hoffer, J. M.

    1973-01-01

    A geological and mineralogical study of the Potrillo volcanics is reported. The investigation consisted first of field mapping to establish and identify the different rock types and volcanic features in order to determine the geological history. Next, samples were collected and analyzed petrographically to determine suitable rocks from the various stratigraphic units for study of plagioclase. Samples selected for further study were crushed and the plagioclase extracted for the determination of composition and structural state. These results were then related to the petrology and crystallization of the basalt.

  11. Synthesis of a spinifex-textured basalt as an analog to Gusev crater basalts, Mars

    NASA Astrophysics Data System (ADS)

    Bost, Nicolas; Westall, Frances; Gaillard, Fabrice; Ramboz, Claire; Foucher, Frédéric

    2012-05-01

    Analyses by the Mars Exploration Rover (MER), Spirit, of Martian basalts from Gusev crater show that they are chemically very different from terrestrial basalts, being characterized in particular by high Mg- and Fe-contents. To provide suitable analog basalts for the International Space Analogue Rockstore (ISAR), a collection of analog rocks and minerals for preparing in situ space missions, especially, the upcoming Mars mission MSL-2011 and the future international Mars-2018 mission, it is necessary to synthesize Martian basalts. The aim of this study was therefore to synthesize Martian basalt analogs to the Gusev crater basalts, based on the geochemical data from the MER rover Spirit. We present the results of two experiments, one producing a quench-cooled basalt (<1 h) and one producing a more slowly cooled basalt (1 day). Pyroxene and olivine textures produced in the more slowly cooled basalt were surprisingly similar to spinifex textures in komatiites, a volcanic rock type very common on the early Earth. These kinds of ultramafic rocks and their associated alteration products may have important astrobiological implications when associated with aqueous environments. Such rocks could provide habitats for chemolithotrophic microorganisms, while the glass and phyllosilicate derivatives can fix organic compounds.

  12. A Re-appraisal of Olivine Sorting and Accumulation in Hawaiian Magmas.

    NASA Astrophysics Data System (ADS)

    Rhodes, J. M.

    2002-12-01

    Bowen never used the m-words (magma mixing) in his highly influential book "The Origin of the Igneous Rocks". Yet, in the past 20-30 years, magma mixing has been proposed as an important, almost ubiquitous, process at volcanoes in all tectonic environments ranging from oceanic basalts to large silicic magma bodies, and as the possible trigger of eruptions. Bowen regarded Hawaiian olivine basalts and picrites as the result of olivine accumulation in a lower MgO magma that was crystallizing and fractionating olivine. This, with variants, has been the party line ever since, the only debate being over the MgO content of the proposed parental magmas. Although magma mixing has been recognized as an important process in differentiated, low-MgO (below 7 percent), Hawaiian magmas, the wide range in MgO (7-30 percent) in Hawaiian olivine tholeiites and picrites is invariably attributed to olivine crystallization, fractionation and accumulation. In this paper I will re-evaluate this hypothesis using well-documented examples from Kilauea, Mauna Kea and Mauna Loa that exhibit well-defined, coherent linear trends of major oxides and trace elements with MgO . If olivine control is the only factor responsible for these trends, then the intersection of the regression lines for each trend should intersect olivine compositions at a common forsterite composition, corresponding to the average accumulated olivine in each of the magmas. In some cases (the ongoing Puu Oo eruption) this simple test holds and olivine fractionation and accumulation can clearly be shown to be the dominant process. In other examples from Mauna Kea and Mauna Loa (1852, 1868, 1950 eruptions, and Mauna Loa in general) the test does not hold, and a more complicated process is required. Additionally, for those magmas that fail the test, CaO/Al2O3 invariably decreases with decreasing MgO content. This should not happen if only olivine fractionation and accumulation are involved. The explanation for these linear

  13. Apollo 12 feldspathic basalts 12031, 12038, and 12072; petrology, comparison and interpretations

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

    Beaty, E.W.; Hill, S.M.R.; Albee, A.L.

    1979-01-01

    Modal and chemical data indicate that 12072, 12038, and 12031, the Apollo 12 feldspathic basalts, form a well-defined group which cannot be related to the other Apollo 12 rock types. 12072 contains phenocrysts of olivine and pigeonite and microphenocrysts of Cr-spinel set in a fine-grained, variolitic groundmass. 12038 is a medium-grained, equigranular basalt with a texture indicating it was multiply saturated. 12031 is a coarse-grained rock with granular to graphic intergrowths of pyroxene and plagioclase; it was also multiply saturated. Petrologic observations, as well as the bulk chemistry, are consistent with the interpretation that 12031 could be derived from 12072more » through fractionation of Cr-spinel, olivine, and pigeonite, the observed phenocryst assemblage. 12038, however, contains more pigeonite, less olivine, three times as much Ca-phosphate minerals, one-fifth as much troilite, and much more sodic plagioclase than 12072. These differences indicate that 12038 must have come from a separate igneous body. Consideration of the bulk compositions indicates that neither 12072 and 12031 nor 12038 could have been derived from the Apollo 12 olivine, pigeonite, or ilmenite basalts by crystal--liquid fractionation. The general petrologic similarities between 12072, 12031, and the other Apollo 12 basalts suggests that they were produced in either the same or similar source regions. 12038, however, is petrologically and chemically unique, and is probably exotic to the Apollo 12 landing site.« less

  14. Mineralogy of the last lunar basalts: Results from Clementine

    USGS Publications Warehouse

    Staid, M.I.; Pieters, C.M.

    2001-01-01

    The last major phase of lunar volcanism produced extensive high-titanium mare deposits on the western nearside which remain unsampled by landing missions. The visible and near-infrared reflectance properties of these basalts are examined using Clementine multispectral images to better constrain their mineralogy. A much stronger 1 ??m ferrous absorption was observed for the western high-titanium basalts than within earlier maria, suggesting that these last major mare eruptions also may have been the most iron-rich. These western basalts also have a distinctly long-wavelength, 1 ??m ferrous absorption which was found to be similar for both surface soils and materials excavated from depth, supporting the interpretation of abundant olivine within these deposits. Spectral variation along flows within the Imbrium basin also suggests variations in ilmenite content along previously mapped lava flows as well as increasing olivine content within subsequent eruptions. Copyright 2001 by the American Geophysical Union.

  15. A Study of Olivine Alteration to Iddingsite Using Raman Spectroscopy

    NASA Technical Reports Server (NTRS)

    Kuebler, K. E.; Wang, Alian; Haskin, L. A.; Jolliff, B. L.

    2003-01-01

    A crucial task of Mars surface science is to determine past environmental conditions, especially aqueous environments and their nature. Identification of mineral alteration by water is one way to do this. Recent work interprets TES spectra as indicating altered basalt on Mars. Olivine, a primary basaltic mineral, is easily altered by aqueous solutions. Alteration assemblages of olivine may be specific to deuteric, hydrothermal, surface water, or metamorphic environments. Raman spectra are produced by molecular vibrations and provide direct means for studying and identifying alteration products. Here, we present a combined study of changes in the chemical composition and Raman spectra of an olivine as it alters to iddingsite. Iddingsite is found in some SNC meteorites and is presumably present on Mars. The term 'iddingsite' has been used as a catch-all term to describe reddish alteration products of olivine, although some authors ascribe a narrower definition: an angstrom-scale intergrowth of goethite and smectite (presumably saponite) formed in an oxidizing and fluid-rich environment. Alteration conserves Fe (albeit oxidized) but requires addition of Al and H2O and removal of Mg and Si. The smectite that forms may be removed by continued alteration. Dehydration of the goethite forms hematite. Our purpose is to study the mineral assemblage, determine the structural and chemical variability of the components with respect to the degree of alteration, and to find spectral indicators of alteration that will be useful during in-situ analyses on Mars.

  16. Os isotope systematics in ocean island basalts

    NASA Astrophysics Data System (ADS)

    Reisberg, Laurie; Zindler, Alan; Marcantonio, Franco; White, William; Wyman, Derek; Weaver, Barry

    1993-12-01

    New Re-Os isotopic results for Os-poor basalts from St. Helena, the Comores, Samoa, Pitcairn and Kerguelen dramatically expand the known range of initial Os-186/Os-187 ratios in Ocean Island Basalts (OIBs) to values as high as 1.7. In contrast to the Os isotopic uniformity of Os-rich basalts from the HIMU islands of Tubuai and Mangaia found by Hauri and Hart, our values for St. Helena span most of the known range of Os isotopic variability in oceanic basalts (initial O-187/Os-186 ranges from 1.2 to 1.7). Generation of such radiogenic Os in the mantle requires melting of source materials that contain large proportions of recycled oceanic crust. The very low Os concentrations of most of the basalts analyzed here, however, leave them susceptible to modification via interaction with materials containing radiogenic Os in the near-surface environment. Thus the high Os-186/Os-187 ratios may result from assimilation of radiogenic Os-rich marine sediments, such as Mn oxides, within the volcanic piles traversed by these magmas en route to the surface. Furthermore, the Os isotopic signatures of Os-rich, olivine-laden OIBs may reflect the accumulation of lithospheric olivine, rather than simply their mantle source characteristics. The extent to which these processes alter the view of the mantle obtained via study of Re-Os systematics in oceanic basalts is uncertain. These effects must be quantified before Re-Os systematics in OIBs can be used with confidence to investigate the nature of mantle heterogeneity and its causes.

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

    NASA Technical Reports Server (NTRS)

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

    2007-01-01

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

  18. Calculation Of Clinopyroxene And Olivine Growth Rates Using Plagioclase Residence Time

    NASA Astrophysics Data System (ADS)

    Kilinc, A. I.; Borell, A.; Leu, A.

    2012-12-01

    According to the Crystal Size Distribution theory (CSD) in a plot of logarithm of number of crystals of a given size range per unit volume [ln(n)], against crystal size [L] shows a straight line. Slope of that line is given by where is the crystal residence time and G is the crystal growth rate. Therefore if is known then G can be calculated. We used thin sections of the Kilauea basalt from Hawaii where olivine, clinopyroxene and plagioclase crystallized within a small temperature range, and the crystal growth rate of plagioclase is known. Assuming that crystal residence times of these three minerals are the same, we plotted ln(n) against L and using the slope and the known crystal growth rate of plagioclase we calculated the crystal growth rates of clinopyroxene and olivine. For the clinopyroxene growth rate we report 10-10.9cm/sec, which is in good agreement with Congdon's data of 10-10 cm/sec. We also calculated the growth rate of olivine is a basaltic melt as 10-8.5 cm/sec which is comparable to < 10-10 to 10-7 cm/sec given by Donaldson and Jambon.

  19. NiO and Fe/Mn in Fo-rich olivines from OIB, MORB, and mantle peridotites

    NASA Astrophysics Data System (ADS)

    Li, H.; Baker, M.; Hofmann, A. E.; Clague, D.; Stolper, E.

    2006-12-01

    Olivines from mantle peridotites have a narrow range of NiO (0.36±0.03 [1σ] wt%), but NiO of olivines in basalts suggest NiO in mantle olivines is actually more variable: e.g., Hawaiian phenocrysts (Fo>90) have NiO >0.55%, and olivines from continental flood basalts can have >0.5% NiO. At the other end of the spectrum, some basaltic suites (e.g., Iceland, MORBs) have Fo>90 olivines with NiO >0.2%. Partial melting calculations on peridotites show it is difficult to generate liquids that crystallize Fo>90 olivines with >0.4% NiO without resorting to complex processes. Hypotheses to explain the variability of NiO in mantle-derived olivines include (1) reaction of peridotite with silica-rich melts of eclogite results in decreasing modal abundance of olivine and increasing NiO in olivine [1,2]; (2) magmas with NiO-rich olivines come from sources enriched in NiO due to a core-derived component [3]. [4] proposed that high Fe/Mn of Hawaiian vs. Icelandic and MORB lavas reflect a core-derived component in their sources. Possible core incorporation is poorly constrained but FeO and NiO are expected to increase by such processes, leading to correlations between NiO and Fe/Mn in mantle rocks with significant core-derived components. We present high-precision analyses of Fo-rich olivines from OIBs, MORBs, komatiites, and mantle peridotites, focusing on NiO contents and Fe/Mn ratios. Our goal is to test hypotheses to explain elevated NiO of Fo-rich olivines in basalts. Olivines are Fo85.1-93.4; more were analyzed, but we focused on this range to avoid complications due to decreasing NiO in olivine with crystallization. Errors (1σ) are 0.01 wt% in NiO and 1.5 in Fe/Mn (wt). Our data show several features: (1) NiO contents and Fe/Mn ratios of Fo>88 olivines are positively correlated, with the low end of the trend (NiO ~0.23%, Fe/Mn ~61) defined by MORB and Iceland and the high end of the trend (NiO ~0.55%, Fe/Mn ~80) by Reunion and Hawaii. Between these end points, there is a

  20. Constraining the timescale of magma stagnation beneath Mauna Kea volcano, Hawaii,using diffusion profiles in olivine phenocrysts

    NASA Astrophysics Data System (ADS)

    Bloch, E. M.; Ganguly, J.

    2009-12-01

    Fe-Mg diffusion profiles have been measured in olivine xenocrysts within alkalic basalts in order to constrain the timescales of magma stagnation beneath Mauna Kea volcano, Hawaii. It has been suggested that during the main tholeiitic shield-building stage, and postshield eruptive stages of Mauna Kea, magmas were stalled and stagnated near the Moho, at a depth of ~15 km. Evidence in support of this hypothesis comes from cumulates formed by gravity-settling and in situ crystallization within magma chambers (Fodor and Galar, 1997), and from clinopyroxene-wholerock thermobarometry on Hamakua basalts (Putirka, in press). The cumulates represent a ‘fossil’ magma chamber which formed primarily from tholeiitic basalts; during the later capping-lava stage of Mauna Kea, alkalic basalts tore off chunks of these cumulates during ascent to the surface. We have measured several diffusion profiles in olivine xenocrysts from a single basalt sample. Because these xenocrysts have homogenous core compositions identical to a neighboring dunite cumulate, and because they are much larger and texturally distinct from compositionally dissimilar olivine phenocrysts, they are interpreted to be cumulate olivines which were dislodged during magma recharge/mixing in the stagnation zone. Although the orientations of the phenocrysts are not yet known, the diffusion profiles have been fit using diffusion coefficients parallel to the c and a crystallographic axes (i.e. minimum and maximum values). Modeling diffusion profiles yields ∫Ddt ≤4.5 x 10-5 cm2. Assuming that the xenocrysts were broken off from the cumulate immediately when the magma chamber was recharged, it is possible to calculate the maximum stagnation time of the basalts. Thus, the retrieved ∫Ddt value yields a maximum stagnation time of ~0.7 years. References: Fodor RV, Galar, PA (1997). A View into the Subsurface of Mauna Kea Volcano, Hawaii: Crystallization Processes Interpreted through the Petrology and Petrography of

  1. Water in Basaltic Melts: an Experimental and Thermodynamic Study of the Effect of H2O on Liquidus Temperatures.

    NASA Astrophysics Data System (ADS)

    Medard, E.; Grove, T. L.

    2006-12-01

    We present a thermodynamic model for the influence of H2O on liquidus temperatures of olivine-saturated primitive basaltic and andesitic melts. The thermodynamic model has been fitted to a suite of H2O-saturated liquidus experiments carried out on a primitive high-alumina basalt from Medicine Lake Volcano (82-72f) over a pressure range of 10 to 1000 MPa. The model of Silver and Stolper (S+S, 1985, J.Geol. 93:161) has been applied to the experimental data. This model uses the assumption of simple ideal mixing between water species and the anionic matrix in the melt. Water in the melt dissolves as molecular H2O, or dissociates to hydroxyl groups and an oxygen atomic network. For 82-72f, the liquidus olivine shows little compositional variability (Fo87.4 to Fo88.4) over the broad range of pressures and temperatures investigated that is not correlated with H2O content of the melt. This observation supports our assumption that major effect of H2O is on the anionic species in the melt and not on the cation equilibria (e.g. Mg and Si). The model reproduces the experimental data well. We find that there is a large influence of H2O addition on melting point for small amounts of H2O, resulting in a concave-down curvature when liquidus depression is plotted against the amount of H2O added. For addition of 0.8 and 5 wt% H2O to 82-72f, the liquidus is depressed by 35 K and 130 K, respectively. The best fits are obtained by assuming partial water dissociation to OH and H2O species, using the equilibrium constant measured by Stolper (1982). S+S applied their model to simple systems (diopside/H2O, albite/H2O, silica/H2O), and recovered the melting behavior extremely well. They also suggested that melt structure/composition influences the amount of liquidus depression caused by H2O addition. We have investigated the influence of bulk composition by performing complementary experiments on a high-magnesian andesite from Mount Shasta, and on a K, Na, and P rich alkali basalt from

  2. Basaltic rocks analyzed by the Spirit Rover in Gusev Crater.

    PubMed

    McSween, H Y; Arvidson, R E; Bell, J F; Blaney, D; Cabrol, N A; Christensen, P R; Clark, B C; Crisp, J A; Crumpler, L S; Des Marais, D J; Farmer, J D; Gellert, R; Ghosh, A; Gorevan, S; Graff, T; Grant, J; Haskin, L A; Herkenhoff, K E; Johnson, J R; Jolliff, B L; Klingelhoefer, G; Knudson, A T; McLennan, S; Milam, K A; Moersch, J E; Morris, R V; Rieder, R; Ruff, S W; De Souza, P A; Squyres, S W; Wänke, H; Wang, A; Wyatt, M B; Yen, A; Zipfel, J

    2004-08-06

    The Spirit landing site in Gusev Crater on Mars contains dark, fine-grained, vesicular rocks interpreted as lavas. Pancam and Mini-Thermal Emission Spectrometer (Mini-TES) spectra suggest that all of these rocks are similar but have variable coatings and dust mantles. Magnified images of brushed and abraded rock surfaces show alteration rinds and veins. Rock interiors contain basalts, containing normative olivine, pyroxenes, plagioclase, and accessory FeTi oxides. Mössbauer, Pancam, and Mini-TES spectra confirm the presence of olivine, magnetite, and probably pyroxene. These basalts extend the known range of rock compositions composing the martian crust.

  3. Basaltic rocks analyzed by the Spirit rover in Gusev crater

    USGS Publications Warehouse

    McSween, H.Y.; Arvidson, R. E.; Bell, J.F.; Blaney, D.; Cabrol, N.A.; Christensen, P.R.; Clark, B. C.; Crisp, J.A.; Crumpler, L.S.; Des Marias, D.J.; Farmer, J.D.; Gellert, Ralf; Ghosh, A.; Gorevan, S.; Graff, T.; Grant, J.; Haskin, L.A.; Herkenhoff, K. E.; Johnson, J. R.; Jolliff, B.L.; Klingelhoefer, G.; Knudson, A.T.; McLennan, S.; Milam, K.A.; Moersch, J.E.; Morris, R.V.; Rieder, R.; Ruff, S.W.; De Souza, P.A.; Squyres, S. W.; Wanke, H.; Wang, A.; Wyatt, M.B.; Yen, A.; Zipfel, J.

    2004-01-01

    The Spirit landing site in Gusev Crater on Mars contains dark, fine-grained, vesicular rocks interpreted as lavas. Pancam and Mini-Thermal Emission Spectrometer (Mini-TES) spectra suggest that all of these rocks are similar but have variable coatings and dust mantles. Magnified images of brushed and abraded rock surfaces show alteration rinds and veins. Rock interiors contain ???25% megacrysts. Chemical analyses of rocks by the Alpha Particle X-ray Spectrometer are consistent with picritic basalts, containing normative olivine, pyroxenes, plagioclase, and accessory FeTi oxides. Mo??ssbauer, Pancam, and Mini-TES spectra confirm the presence of olivine, magnetite, and probably pyroxene. These basalts extend the known range of rock compositions composing the martian crust.

  4. Basaltic rocks analyzed by the Spirit Rover in Gusev Crater

    NASA Technical Reports Server (NTRS)

    McSween, H. Y.; Arvidson, R. E.; Bell, J. F., III; Blaney, D.; Cabrol, N. A.; Christensen, P. R.; Clark, B. C.; Crisp, J. A.; Crumpler, L. S.; DesMarais, D. J.; hide

    2004-01-01

    The Spirit landing site in Gusev Crater on Mars contains dark, fine-grained, vesicular rocks interpreted as lavas. Pancam and Mini-Thermal Emission Spectrometer (Mini-TES) spectra suggest that all of these rocks are similar but have variable coatings and dust mantles. Magnified images of brushed and abraded rock surfaces show alteration rinds and veins. Rock interiors contain basalts, containing normative olivine, pyroxenes, plagioclase, and accessory FeTi oxides. Mossbauer, Pancam, and Mini-TES spectra confirm the presence of olivine, magnetite, and probably pyroxene. These basalts extend the known range of rock compositions composing the martian crust.

  5. Cumulate xenoliths from St. Vincent, Lesser Antilles Island Arc: a window into upper crustal differentiation of mantle-derived basalts

    NASA Astrophysics Data System (ADS)

    Tollan, P. M. E.; Bindeman, I.; Blundy, J. D.

    2012-02-01

    In order to shed light on upper crustal differentiation of mantle-derived basaltic magmas in a subduction zone setting, we have determined the mineral chemistry and oxygen and hydrogen isotope composition of individual cumulus minerals in plutonic blocks from St. Vincent, Lesser Antilles. Plutonic rock types display great variation in mineralogy, from olivine-gabbros to troctolites and hornblendites, with a corresponding variety of cumulate textures. Mineral compositions differ from those in erupted basaltic lavas from St. Vincent and in published high-pressure (4-10 kb) experimental run products of a St. Vincent high-Mg basalt in having higher An plagioclase coexisting with lower Fo olivine. The oxygen isotope compositions (δ18O) of cumulus olivine (4.89-5.18‰), plagioclase (5.84-6.28‰), clinopyroxene (5.17-5.47‰) and hornblende (5.48-5.61‰) and hydrogen isotope composition of hornblende (δD = -35.5 to -49.9‰) are all consistent with closed system magmatic differentiation of a mantle-derived basaltic melt. We employed a number of modelling exercises to constrain the origin of the chemical and isotopic compositions reported. δ18OOlivine is up to 0.2‰ higher than modelled values for closed system fractional crystallisation of a primary melt. We attribute this to isotopic disequilibria between cumulus minerals crystallising at different temperatures, with equilibration retarded by slow oxygen diffusion in olivine during prolonged crustal storage. We used melt inclusion and plagioclase compositions to determine parental magmatic water contents (water saturated, 4.6 ± 0.5 wt% H2O) and crystallisation pressures (173 ± 50 MPa). Applying these values to previously reported basaltic and basaltic andesite lava compositions, we can reproduce the cumulus plagioclase and olivine compositions and their associated trend. We conclude that differentiation of primitive hydrous basalts on St. Vincent involves crystallisation of olivine and Cr-rich spinel at depth

  6. Genetic relations of oceanic basalts as indicated by lead isotopes

    USGS Publications Warehouse

    Tatsumoto, M.

    1966-01-01

    The isotopic compositions of lead and the concentrations of lead, uranium, and thorium in samples of oceanic tholeiite and alkali suites are determined, and the genetic relations of the oceanic basalts are discussed. Lead of the oceanic tholeiites has a varying lead-206 : lead-204 ratio between 17.8 and 18.8, while leads of the alkali basalt suites from Easter Island and Guadalupe Island are very radiogenic with lead-206 : lead-204 ratios between 19.3 and 20.4. It is concluded that (i) the isotopic composition of lead in oceanic tholeiite suggests that the upper mantle source region of the tholeiite was differentiated from an original mantle material more than 1 billion years ago and that the upper mantle is not homogeneous at the present time, (ii) less than 20 million years was required for the crystal differentiation within the alkali suite from Easter Island, (iii) no crustal contamination was involved in the course of differentiation of rocks from Easter Island; however, some crustal contamination may have affected Guadalupe Island rocks, and (iv) alkali basalt may be produced from the tholeiite in the oceanic region by crystal differentiation. Alternatively the difference in the isotopic composition of lead in oceanic basalts may be produced by partial melting at different depths of a differentiated upper mantle.

  7. 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

  8. Platinum-Group Elements in Basalts Derived From the Icelandic Mantle Plume -Past and Present.

    NASA Astrophysics Data System (ADS)

    Momme, P.; Oskarsson, N.; Gronvold, K.; Tegner, C.; Brooks, K.; Keays, R.

    2001-12-01

    Paleogene basalts ( ~55Ma) derived from the ancestral Iceland mantle plume and extruded during continental rifting are exposed along the Blosseville Kyst in central East Greenland. These basalts comprise three intercalated series, viz: a low-Ti, high-Ti and a very high-Ti series. The two Ti-rich series are interpreted to represent continental flood basalts formed by low degrees of partial melting (degree of melting F=3-9%) while the low-Ti series are believed to have formed by higher degrees of partial melting (F:15-25%). All three of the East Greenland basalt series are enriched in the PGE, relative to normal MORB. During differentiation of the low-Ti series, Pd increase from 11 to 24 ppb whereas Pt and Ir decrease from 12 and 0.6 ppb to 3 and <0.05 ppb respectively. The primitive basalts (molar Mg#60) of the dominant high-Ti series contain ~6-10 ppb Pd, ~7-10 ppb Pt and ~0.2 ppb Ir whereas the most evolved basalts (Mg#43) contain 25 ppb Pd, 5 ppb Pt and <0.05 ppb Ir. The PGE-rich nature of these basalts is surprising because low degree partial melts are generally S-saturated and hence strongly depleted in the PGE (cf, Keays, 1995). However, our data indicates that all of the East Greenland magmas were S-undersaturated and as they underwent differentiation, Pd behaved incompatibly while Ir and Pt behaved compatibly. Primitive Holocene Icelandic olivine tholeiites contain 120 ppm Cu, 6 ppb Pd, 4 ppb Pt and 0.2 ppb Ir while their picritic counterparts contain 74 ppm Cu, 17 ppb Pd, 7 ppb Pt and 0.3 ppb Ir. Both the olivine tholeiites and the picrites are believed to have formed by high degrees of partial melting (15-25%) which would have exhausted all of the sulphides in the mantle source region and produced S-undersaturated magmas. In Icelandic samples with 10-14wt% MgO, Cu and the PGEs vary systematically between the primitive picrite and olivine tholeiite compositions given above i.e there is an inverse correlation between Cu and the PGEs. This is best explained

  9. Petrogenesis of the Northwest Africa 4898 high-Al mare basalt

    NASA Astrophysics Data System (ADS)

    Li, Shaolin; Hsu, Weibiao; Guan, Yunbin; Wang, Linyan; Wang, Ying

    2016-07-01

    Northwest Africa (NWA) 4898 is the only low-Ti, high-Al basaltic lunar meteorite yet recognized. It predominantly consists of pyroxene (53.8 vol%) and plagioclase (38.6 vol%). Pyroxene has a wide range of compositions (En12-62Fs25-62Wo11-36), which display a continuous trend from Mg-rich cores toward Ca-rich mantles and then to Fe-rich rims. Plagioclase has relatively restricted compositions (An87-96Or0-1Ab4-13), and was transformed to maskelynite. The REE zoning of all silicate minerals was not significantly modified by shock metamorphism and weathering. Relatively large (up to 1 mm) olivine phenocrysts have homogenous inner parts with Fo ~74 and sharply decrease to 64 within the thin out rims (~30 μm in width). Four types of inclusions with a variety of textures and modal mineralogy were identified in olivine phenocrysts. The contrasting morphologies of these inclusions and the chemical zoning of olivine phenocrysts suggest NWA 4898 underwent at least two stages of crystallization. The aluminous chromite in NWA 4898 reveals that its high alumina character was inherited from the parental magma, rather than by fractional crystallization. The mineral chemistry and major element compositions of NWA 4898 are different from those of 12038 and Luna 16 basalts, but resemble those of Apollo 14 high-Al basalts. However, the trace element compositions demonstrate that NWA 4898 and Apollo 14 high-Al basalts could not have been derived from the same mantle source. REE compositions of its parental magma indicate that NWA 4898 probably originated from a unique depleted mantle source that has not been sampled yet. Unlike Apollo 14 high-Al basalts, which assimilated KREEPy materials during their formation, NWA 4898 could have formed by closed-system fractional crystallization.

  10. Crystal Stratigraphy of Two Basalts from Apollo 16: Unique Crystallization of Picritic Basalt 606063,10-16 and Very-Low-Titanium Basalt 65703,9-13

    NASA Technical Reports Server (NTRS)

    Donohue, P. H.; Neal, C. R.; Stevens, R. E.; Zeigler, R. A.

    2014-01-01

    A geochemical survey of Apollo 16 regolith fragments found five basaltic samples from among hundreds of 2-4 mm regolith fragments of the Apollo 16 site. These included a high-Ti vitrophyric basalt (60603,10-16) and one very-low-titanium (VLT) crystalline basalt (65703,9-13). Apollo 16 was the only highlands sample return mission distant from the maria (approx. 200 km). Identification of basaltic samples at the site not from the ancient regolith breccia indicates input of material via lateral transport by post-basin impacts. The presence of basaltic rocklets and glass at the site is not unprecedented and is required to satisfy mass-balance constraints of regolith compositions. However, preliminary characterization of olivine and plagioclase crystal size distributions indicated the sample textures were distinct from other known mare basalts, and instead had affinities to impact melt textures. Impact melt textures can appear qualitatively similar to pristine basalts, and quantitative analysis is required to distinguish between the two in thin section. The crystal stratigraphy method is a powerful tool in studying of igneous systems, utilizing geochemical analyses across minerals and textural analyses of phases. In particular, trace element signatures can aid in determining the ultimate origin of these samples and variations document subtle changes occurring during their petrogenesis.

  11. Diffusion-driven magnesium and iron isotope fractionation in Hawaiian olivine

    USGS Publications Warehouse

    Teng, F.-Z.; Dauphas, N.; Helz, R.T.; Gao, S.; Huang, S.

    2011-01-01

    Diffusion plays an important role in Earth sciences to estimate the timescales of geological processes such as erosion, sediment burial, and magma cooling. In igneous systems, these diffusive processes are recorded in the form of crystal zoning. However, meaningful interpretation of these signatures is often hampered by the fact that they cannot be unambiguously ascribed to a single process (e.g., magmatic fractionation, diffusion limited transport in the crystal or in the liquid). Here we show that Mg and Fe isotope fractionations in olivine crystals can be used to trace diffusive processes in magmatic systems. Over sixty olivine fragments from Hawaiian basalts show isotopically fractionated Mg and Fe relative to basalts worldwide, with up to 0.4??? variation in 26Mg/24Mg ratios and 1.6??? variation in 56Fe/54Fe ratios. The linearly and negatively correlated Mg and Fe isotopic compositions [i.e., ??56Fe=(??3.3??0.3)????26Mg], co-variations of Mg and Fe isotopic compositions with Fe/Mg ratios of olivine fragments, and modeling results based on Mg and Fe elemental profiles demonstrate the coupled Mg and Fe isotope fractionation to be a manifestation of Mg-Fe inter-diffusion in zoned olivines during magmatic differentiation. This characteristic can be used to constrain the nature of mineral zoning in igneous and metamorphic rocks, and hence determine the residence times of crystals in magmas, the composition of primary melts, and the duration of metamorphic events. With improvements in methodology, in situ isotope mapping will become an essential tool of petrology to identify diffusion in crystals. ?? 2011 Elsevier B.V.

  12. Dissolution of Olivine, Siderite, and Basalt at 80 Deg C in 0.1 M H2SO4 in a Flow Through Process: Insights into Acidic Weathering on Mars

    NASA Technical Reports Server (NTRS)

    Golden, D. C.; Ming, D. W.; Hausrath, E. M.; Morris, R. V.; Niles, P. B.; Achilles, C. N.; Ross, D. K.; Cooper, B. L.; Gonzalex, C. P.; Mertzman, S. A.

    2012-01-01

    The occurrence of jarosite, other sulfates (e.g., Mg-and Ca-sulfates), and hematite along with silicic-lastic materials in outcrops of sedimentary materials at Meridiani Planum (MP) and detection of silica rich deposits in Gusev crater, Mars, are strong indicators of local acidic aqueous processes [1,2,3,4,5]. The formation of sediments at Meridiani Planum may have involved the evaporation of fluids derived from acid weathering of Martian basalts and subsequent diagenesis [6,7]. Also, our previous work on acid weathering of basaltic materials in a closed hydro-thermal system was focused on the mineralogy of the acid weathering products including the formation of jarosite and gray hematite spherules [8,9,10]. The object of this re-search is to extend our earlier qualitative work on acidic weathering of rocks to determine acidic dissolution rates of Mars analog basaltic materials at 80 C using a flow-thru reactor. We also characterized residual phases, including poorly crystalline or amorphous phases and precipitates, that remained after the treatments of olivine, siderite, and basalt which represent likely MP source rocks. This study is a stepping stone for a future simulation of the formation of MP rocks under a range of T and P.

  13. Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

    USGS Publications Warehouse

    Stern, C.R.; Frey, F.A.; Futa, K.; Zartman, R.E.; Peng, Z.; Kurtis, Kyser T.

    1990-01-01

    The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc

  14. Pliocene-Quaternary basalts from the Harrat Tufail, western Saudi Arabia: Recycling of ancient oceanic slabs and generation of alkaline intra-plate magma

    NASA Astrophysics Data System (ADS)

    Bakhsh, Rami A.

    2015-12-01

    Harrat Tufail represents a Caenozoic basalt suite at the western margin of the Arabian plate. This rift-related suite includes voluminous Quaternary non-vesicular basalt (with fragments of earlier Pliocene vesicular flow) that forms a cap sheet over Miocene rhyolite and minor vesicular basalt. The contact between rhyolite and the basaltic cap is erosional with remarkable denudations indicating long time gap between the felsic and mafic eruptions. The geochemical data prove alkaline, sodic and low-Ti nature of the olivine basalt cap sheet. The combined whole-rock and mineral spot analyses by the electron microprobe (EMPA) suggest magma generation from low degree of partial melting (∼5%) from spinel- and garnet-lherzolite mantle source. Derivation from a mantle source is supported by low Na content in clinopyroxene (ferroan diopside) whereas high Mg content in ilmenite is an evidence of fractional crystallization trajectory. Accordingly, the Pliocene basaltic cap of Harrat Tufail is a product of mantle melt that originates by recycling in the asthenosphere during subduction of ancient oceanic slab(s). The whole-rock chemistry suggests an ancient ocean island basaltic slab (OIB) whereas the EMPA of Al-rich spinel inclusions in olivine phenocrysts are in favour of a mid-ocean ridge basaltic source (MORB). Calculations of oxygen fugacity based on the composition of co-existing Fe-Ti oxide suggest fluctuation from highly to moderately oxidizing conditions with propagation of crystallization (log10 fO2 from -22.09 to -12.50). Clinopyroxene composition and pressure calculation indicates low-pressure (0.4-2 kbar). Cores of olivine phenocrysts formed at highest temperature (1086-1151 °C) whereas the rims and olivine micro-phenocrysts formed at 712-9-796 °C which is contemporaneous to formation of clinopyroxene at 611-782 °C. Fe-Ti oxides crystallized over a long range (652-992 °C) where it started to form at outer peripheries of olivine phenocrysts and as interstitial

  15. Th-230 - U-238 series disequilibrium of the Olkaria basalts Gregory Rift Valley, Kenya

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

    U-Th disequilibrium analyses of the Naivasha basalts show a very small (U-238/Th-230) ratios which are lower than any previously analyzed basalts. The broadly positive internal isochron trend from one sample indicates that the basalts may have source heterogeneities, this is supported by earlier work. The Naivasha complex comprises a bimodal suite of basalts and rhyolites. The basalts are divided into two stratigraphic groups each of a transitional nature. The early basalt series (EBS) which were erupted prior to the Group 1 comendites and, the late basalt series (LBS) which erupted temporally between the Broad Acres and the Ololbutot centers. The basalts represent a very small percentage of the overall eruptive volume of material at Naivasha (less than 2 percent). The analyzed samples come from four stratigraphic units in close proximity around Ndabibi, Hell's Gate and Akira areas. The earliest units occur as vesicular flows from the Ndabibi plain. These basalts are olivine-plagioclase phyric with the associated hawaiites being sparsely plagioclase phyric. An absolute age of 0.5Ma was estimated for these basalts. The next youngest basalts flows occur as younger tuft cones in the Ndabibi area and are mainly olivine-plagioclase-clinopyroxcene phyric with one purely plagioclase phyric sample. The final phase of activity at Ndabibi resulted in much younger tuft cones consisting of air fall ashes and lapilli tufts. Many of these contain resorbed plagioclase phenocrysts with sample number 120c also being clinopyroxene phyric. The isotopic evidence for the basalt formation is summarized.

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

    NASA Astrophysics Data System (ADS)

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

    2006-03-01

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

  17. Stabilization of Lithium Transition Metal Silicates in the Olivine Structure

    DOE PAGES

    Sun, Xiaoqi; Tripathi, Rajesh; Popov, Guerman; ...

    2017-07-28

    While olivine LiFePO 4 shows amongst the best electrochemical properties of Li-ion positive electrodes with respect to rate behavior owing to facile Li + migration pathways in the framework, replacing the [PO 4] 3- polyanion with a silicate [SO 4] 4- moitie in olivine is desirable. This would allow additional balancing alkali content and hence electron transfer, and increase the capacity. We demonstrate the first stabilization of a lithium transition-metal silicate (as a pure silicate) in the olivine structure type. Using LiInSiO 4 and LiScSiO 4 as the parent materials, transition metal (Mn, Fe, Co) substitutions on the In/Sc sitemore » were investigated by computational modelling via atomic scale simulation. Transition metal substitution was found to be only favourable for Co, a finding confirmed by the successful solid state synthesis of olivine LixInyCo 2-x-ySiO 4. Finally, the stabilization of the structure was achieved by entropy provided by cation disorder.« less

  18. Lu-Hf AND Sm-Nd EVOLUTION IN LUNAR MARE BASALTS.

    USGS Publications Warehouse

    Unruh, D.M.; Stille, P.; Patchett, P.J.; Tatsumoto, M.

    1984-01-01

    Lu-Hf and Sm-Nd data for mare basalts combined with Rb-Sr and total REE data taken from the literature suggest that the mare basalts were derived by small ( less than equivalent to 10%) degrees of partial melting of cumulate sources, but that the magma ocean from which these sources formed was light REE and hf-enriched. Calculated source compositions range from lherzolite to olivine websterite. Nonmodal melting of small amounts of ilmenite ( less than equivalent to 3%) in the sources seems to be required by the Lu/Hf data. A comparison of the Hf and Nd isotopic characteristics between the mare basalts and terrestrial oceanic basalts reveals that the epsilon Hf/ epsilon Nd ratios in low-Ti mare basalts are much higher than in terrestrial ocean basalts.

  19. Temperatures and Melt Water Contents at the Onset of Phenocryst Growth in Quaternary Nepheline-Normative Basalts Erupted along the Tepic-Zacoalco Rift in Western Mexico

    NASA Astrophysics Data System (ADS)

    Mesa, J.; Lange, R. A.; Pu, X.

    2017-12-01

    Nepheline-normative, high-Mg basalts erupted from the western Mexican arc, along the Tepic-Zacoalco rift (TZR), have a trace-element signature consistent with an asthenosphere source, whereas calc-alkaline basalts erupted from the central Mexican arc in the Michoacan-Guanajuato volcanic field (MGVF) have a trace-element signature consistent with a mantle source strongly affected by subduction fluids. In this study, olivine-melt thermometry and plagioclase-liquid hygrometry are used to constrain the temperature and melt water content of the alkaline TZR basalts. The presence of diffusion-limited growth textures in olivine and plagioclase phenocrysts provide preliminary evidence of rapid growth during ascent. For each basalt sample, a histogram of all analyzed olivines in each sample allows the most Fo-rich composition to be identified, which matches the calculated composition at the liquidus via MELTS (Ghiorso & Sack, 1995; Asimow & Ghiorso, 1998) at fO2 values of QFM +2. Therefore a newly developed olivine-melt thermometer, based on DNiol/liq (Pu et al., 2017) was used to calculate temperature at the onset of olivine crystallization during ascent. Temperatures range from 1076-1247°C, whereas those calculated using an olivine-melt thermometer based on DMgol/liq range from 1141-1236 °C. Olivine-melt thermometers based on DMgol/liq are sensitive to melt H2O content, therefore ΔT = TMg - TNi (≤ 82 degrees) may be used as a qualitative indicator of melt H2O (≤ 2.6 wt% H2O; Pu et al., 2017). When temperatures from the Ni-thermometer are applied to the most calcic plagioclase in each sample (Waters & Lange, 2015), calculated melt H2O contents range from 1.3-1.9 (± 0.4) wt%. These values are significantly lower than those obtained from high-Mg calc-alkaline basalts from the MGVF using similar methods (1.9-5.0 wt%; Pu et al., 2017), consistent with a reduced involvement of slab-derived fluids in the origin of the alkaline TZR basalts from western Mexico.

  20. Is formation segregation melts in basaltic lava flows a viable analogue to melt generation in basaltic systems?

    NASA Astrophysics Data System (ADS)

    Thordarson, Thorvaldur; Sigmarsson, Olgeir; Hartley, Margaret E.; Miller, Jay

    2010-05-01

    Pahoehoe sheet lobes commonly exhibit a three-fold structural division into upper crust, core and lower crust, where the core corresponds to the liquid portion of an active lobe sealed by crust. Segregations are common in pahoehoe lavas and are confined to the core of individual lobes. Field relations and volume considerations indicate that segregation is initiated by generation of volatile-rich melt at or near the lower crust to core boundary via in-situ crystallization. Once buoyant, the segregated melt rises through the core during last stages of flow emplacement and accumulates at the base of the upper crust. The segregated melt is preserved as vesicular and aphyric, material within well-defined vesicle cylinders and horizontal vesicle sheets that make up 1-4% of the total lobe volume. We have undertaken a detailed sampling and chemical analysis of segregations and their host lava from three pahoehoe flow fields; two in Iceland and one in the Columbia River Basalt Group (CRBG). The Icelandic examples are: the olivine-tholeiite Thjorsa lava (24 cubic km) of the Bardarbunga-Veidivotn volcanic system and mildly alkalic Surtsey lavas (1.2 cubic km) of the Vestmannaeyjar volcanic system. The CRBG example is the tholeiitic ‘high-MgO group' Levering lava (>100? cubic km) of the N2 Grande Ronde Basalt. The thicknesses of the sampled lobes ranges from 2.3 to 14 m and each lobe feature well developed network of segregation structures [1,2,3]. Our whole-rock analyses show that the segregated melt is significantly more evolved than the host lava, with enrichment factors of 1.25 (Thjorsa) to 2.25 (Surtsey) for incompatible trace elements (Ba, Zr). Calculations indicate that the segregation melt was formed by 20 to 50% closed-system fractional crystallization of plagioclase (plus minor pyroxene and/or olivine). A more striking feature is the whole-rock composition of the segregations. In the olivine-tholeiite Thjorsa lava the segregations exhibit quartz tholeiite

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

    NASA Astrophysics Data System (ADS)

    Sharkov, Evgenii

    2015-04-01

    It is consensus now that within-plate magmatism is considered with ascending of mantle plumes and adiabatic melting of their head. At the same time composition of the plumes' matter and conditions of its adiabatic melting are unclear yet. The major source of objective information about it can be mantle xenoliths in alkali basalts and basanites which represent fragments of material of the plume heads above magma-generation zone. They are not represent material in melting zone, however, carry important information about material of modern mantle plumes, its phase composition and components, involved in melting. Populations of mantle xenoliths in basalts are characterized by surprising sameness in the world and represented by two major types: (1) dominated rocks of ``green'' series, and (2) more rare rocks of ``black'' series, which formed veins in the ``green'' series matrix. It can evidence about common composition of plume material in global scale. In other words, the both series of xenoliths represent two types of material of thermochemical mantle plumes, ascended from core-mantle boundary (Maruyama, 1994; Dobretsov et al., 2001). The same types of xenoliths are found in basalts and basanites of Western Syria (Sharkov et al., 1996). Rocks of ``green'' series are represented by Sp peridotites with cataclastic and protogranular structures and vary in composition from dominated spinel lherzolites to spinel harzburgites and rare spinel pyroxenites (websterites). It is probably evidence about incomplete homogenizing of the plume head matter, where material, underwent by partial melting, adjoins with more fertile material. Such heterogeneity was survived due to quick cooling of upper rim of the plume head in contact with relatively cold lithosphere. Essential role among xenoliths of the ``black'' series play Al-Ti-augite and water-bearing phases like hornblende (kaersutute) and Ti-phlogopite. Rocks of this series are represented by wehrlite, clinopyroxenite, amphibole

  2. Petrology of basaltic sills from ocean drilling program sites 794 and 797 in the Yamato Basin of the Japan Sea

    NASA Technical Reports Server (NTRS)

    Thy, P.

    1992-01-01

    The basaltic sills from ocean drilling program sites 794 and 797 in the Yamato Basin of the Japan Sea are characterized petrographically on the basis of a detailed study of the composition of relict phenocryst and groundmass phases. The systematic variation in the rock compositions is discussed. Results of 1-atm melting experiments on a relatively primitive basalt from site 797 are reported. The sills are found to constitute two distinct groups of suites: primitive, olivine-bearing suites with low potassium and primitive olivine-bearing to evolved, olivine-free suites with relatively high potassium. A pseudoinvariant reaction relationship between olivine and augite and magnetite is inferred. Complex magmatic and tectonic evolutions in the region, perhaps reflecting a transitional stage between subduction zone activity and back arc spreading, are suggested.

  3. Inherited Pb isotopic records in olivine antecryst-hosted melt inclusions from Hawaiian lavas

    NASA Astrophysics Data System (ADS)

    Sakyi, Patrick Asamoah; Tanaka, Ryoji; Kobayashi, Katsura; Nakamura, Eizo

    2012-10-01

    Dislocation textures of olivine grains and Pb isotopic compositions (207Pb/206Pb and 208Pb/206Pb) of olivine-hosted melt inclusions in basaltic lavas from three Hawaiian volcanoes (Kilauea, Mauna Loa, and Koolau) were examined. More than 70% of the blocky olivine grains in the studied samples have a regular-shaped dislocation texture with their dislocation densities exceeding 106 cm-2, and can be considered as deformed olivine. The size distribution of blocky olivine grains shows that more than 99% of blocky olivines coarser than 1.2 mm are identified as deformed olivine. These deformed olivine grains are identified as antecrysts, which originally crystallized from previous stages of magmatism in the same shield, followed by plastic deformation prior to entrainment in the erupted host magmas. This study revealed that entrainment of mantle-derived crystallization products by younger batches of magma is an important part of the evolution of magnesium-rich Hawaiian magma. Lead isotopic compositions of melt inclusions hosted in the olivine antecrysts provide information of the evolutionary history of Hawaiian volcanoes which could not have been accessed if only whole rock analyses were carried out. Antecryst-hosted melt inclusions in Kilauea and Koolau lavas demonstrate that the source components in the melting region changed during shield formation. In particular, evidence of interaction of plume-derived melts and upper mantle was observed in the earliest stage of Koolau magmatism.

  4. Assessing δ18O heterogeneity in Icelandic olivine crystals

    NASA Astrophysics Data System (ADS)

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

    2017-12-01

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

  5. Experimentally reproduced textures and mineral chemistries of high-titanium mare basalts

    NASA Technical Reports Server (NTRS)

    Usselman, T. M.; Lofgren, G. E.; Williams, R. J.; Donaldson, C. H.

    1975-01-01

    Many of the textures, morphologies, and mineral chemistries of the high-titanium mare basalts have been experimentally duplicated using single-stage cooling histories. Lunar high-titanium mare basalts are modeled in a 1 m thick gravitationally differentiating flow based on cooling rates, thermal models, and modal olivine contents. The low-pressure equilibrium phase relations of a synthetic high-titanium basalt composition were investigated as a function of oxygen fugacity, and petrographic criteria are developed for the recognition of phenocrysts which were present in the liquid at the time of eruption.

  6. Rocks Whose Compositions are Determined by Flow Differentiation of Olivine- and Sulfide Droplet-Laden Magma: the Jinchuan Story

    NASA Astrophysics Data System (ADS)

    Li, C.; Ripley, E. M.; de Waal, S. A.; Xu, Z.

    2002-12-01

    The Jinchuan intrusion in western China is an elongated, deeply-dipping dyke-like body of dominantly olivine-rich ultramafic rocks of high magnesium basaltic magma. It hosts the second largest Ni-Cu sulfide deposit in the world. More than 500 million tones of sulfide ore grading 1.2 percent Ni and 0.7 percent Cu occur mostly as next-textured and disseminated sulfide (pyrrhotite, pentlendite and chalcopyrite) with cumulus olivine in about half of the rocks of the intrusion. Based on different petrological zonations, the Jinchuan intrusion is further divided into three segments: eastern, central and western segments. The central segment is characterized by concentric enrichments of cumulus olivine and sulfide, whereas the eastern and western segments are characterized by the increase of both cumulus olivine and sulfide toward the footwall. The forsterite contents of fresh olivine from different segments are similar and vary between 82 and 86 mole percent. The small range of olivine compositional variation corresponds to less than 6 percent of fractional crystallization. Mass balance calculations based on sulfide solubility in basaltic magma indicate that the volume of the parental magma of the sulfide is many times larger than that which is currently represented in the intrusion. Large amounts of cumulus olivine (more than 40 weight percent) in the marginal samples and high concentrations of sulfide in the intrusion are consistent with an interpretation that the Jinchuan intrusion was formed by olivine- and sulfide droplet-laden magma ascending through a subvertical conduit to a higher level. Differentiation processes of the olivine- and sulfide droplet-laden magma varied in different parts of the conduit. Sub-vertical flow differentiation controlled the central segment of the conduit, resulting in further enrichment of olivine crystals and sulfide droplets in the conduit center. In contrast, sub-lateral flow and gravitational differentiation dominated in the eastern

  7. Rare-earth element geochemistry and the origin of andesites and basalts of the Taupo Volcanic Zone, New Zealand

    USGS Publications Warehouse

    Cole, J.W.; Cashman, K.V.; Rankin, P.C.

    1983-01-01

    Two types of basalt (a high-Al basalt associated with the rhyolitic centres north of Taupo and a "low-Al" basalt erupted from Red Crater, Tongariro Volcanic Centre) and five types of andesite (labradorite andesite, labradorite-pyroxene andesite, hornblende andesite, pyroxene low-Si andesite and olivine andesite/low-Si andesite) occur in the Taupo Volcanic Zone (TVZ), North Island, New Zealand. Rare-earth abundances for both basalts and andesites are particularly enriched in light rare-earth elements. High-Al basalts are more enriched than the "low-Al" basalt and have values comparable to the andesites. Labradorite and labradorite-pyroxene andesites all have negative Eu anomalies and hornblende andesites all have negative Ce anomalies. The former is probably due to changing plagioclase composition during fractionation and the latter to late-stage hydration of the magma. Least-squares mixing models indicate that neither high-Al nor "low-Al" basalts are likely sources for labradorite/labradorite-pyroxene andesites. High-Al basalts are considered to result from fractionation of olivine and clinopyroxene from a garnet-free peridotite at the top of the mantle wedge. Labradorite/labradorite-pyroxene andesites are mainly associated with an older NW-trending arc. The source is likely to be garnet-free but it is not certain whether the andesites result from partial melting of the top of the subducting plate or a hydrated lower portion of the mantle wedge. Pyroxene low-Si andesites probably result from cumulation of pyroxene and calcic plagioclase within labradorite-pyroxene andesites, and hornblende andesites by late-stage hydration of labradorite-pyroxene andesite magma. Olivine andesites, low-Si andesites and "low-Al" basalts are related to the NNE-trending Taupo-Hikurangi arc structure. Although the initial source material is different for these lavas they have probably undergone a similar history to the labradorite/labradorite-pyroxene andesites. All lavas show evidence

  8. Olivine-Rich Troctolite from the Southwest Indian Ridge: Constrains on Melt-Rock Reaction beneath Mid-Ocean Ridges

    NASA Astrophysics Data System (ADS)

    Yang, A. Y.

    2017-12-01

    The origin of olivine-rich troctolite, which have been recovered in the plutonic sample suites from the fast-spreading East Pacific Rise, and slow-spreading Mid-Atlantic Ridge and Central Indian Ridge, has been highly debated. They can form either by fractionation of primitive mid-ocean ridge basalt (MORB) melts or by melt migrating through pre-existing (possibly mantle) olivine matrix, thus recording valuable information of magmatic process at mantle-crust transition. This study presents in situ major and trace element study on the olivine-rich troctolite first reported from the ultraslow-spreading Southwest Indian Ridge (SWIR), together with a series of samples from peridotite, gabbro to basalt from an amagmatic segment at 53°E during Dayangyihao Cruises, to investigate the magmatic processes occurred at mantle-crust transition and origin of olivine-rich troctolite. The olivine in the troctolite shows cumulate textures with interstitial clinopyroxene, plagioclase and minor spinel, which is cross-cut by an olivine gabbro vein. Olivine in the troctolite show only mildly decreasing NiO contents (from 0.31-0.25 wt.%) with decreasing Fo (from 86 to 81), and even olivine in the gabbro have NiO up to 0.24 wt.% with Fo of 75. The Fo vs. Ni correlation of olivine is shifted to uniquely higher NiO at a certain Fo compared to the trends defined by either olivine from other lower oceanic crust (LOC) cumulates worldwide or olivine compositions from classic fractionation model for primitive MORB magma. Interstitial clinopyroxene in the troctolite have high Mg# (88-90), Cr2O3 (up to 1.51 wt.%) and TiO2 contents (up to 1.01 wt.%) with Eu/Eu* from 0.4-0.6. Such high-Ti-Cr-Mg# clinopyroxene is rare among global LOC cumulates, and cannot result from simple fractionation of MORB magma. The mineral compositions in the olivine-rich troctolite could be modeled by reaction between a primitive olivine matrix and a highly evolved melt (with 2.4 wt.% TiO2), and such a melt composition is

  9. Temporal helium isotopic variations within Hawaiian volcanoes: Basalts from Mauna Loa and Haleakala

    NASA Astrophysics Data System (ADS)

    Kurz, Mark D.; Garcia, Michael O.; Frey, Fred A.; O'Brien, P. A.

    1987-11-01

    Helium isotope ratios in basalts spanning the subaerial eruptive history of Mauna Loa and Haleakala vary systematically with eruption age. In both volcanoes, olivine mineral separates from the oldest samples have the highest 3He /4He ratios. The Haleakala samples studied range in age from roughly one million years to historic time, while the Mauna Loa samples are radiocarbon dated flows younger than 30.000 years old. The Honomanu tholeiites are the oldest samples from Haleakala and have 3He /4He ratios that range from 13 to 16.8× atmospheric, while the younger Kula and Hana series alkali basalts all have 3He /4He close to 8×atmospheric. A similar range is observed on Mauna Loa; the oldest samples (roughly 30,000 years) have 3He /4He ratios of 15 to 20 × atmospheric, with a relatively smooth decrease to 8 × atmospheric with decreasing age. The consistent trend of decreasing 3He/ 4He ratio with time in both volcanoes, coherence between the helium and Sr and Nd isotopes (for Haleakala), and the similarity of 3He /4He in the late stage basalts to depleted mid-ocean ridge basalt (MORB) helium, argue against the decrease being the result of radiogenic ingrowth of 4He. The data strongly suggest an undegassed ( i.e., high 3He/(Th + U)) mantle source for the early shield building stages of Hawaiian volcanism. and are consistent with the hotspot/mantle plume model. The data are difficult to reconcile with models for Hawaiian volcanism that require recycled oceanic crust or derivation from a MORB-related upper mantle source. We interpret the decrease in 3He /4He with volcano evolution to result from an increasing involvement of depleted mantle and/or lithosphere during the late stages of Hawaiian volcanism.

  10. Origin of primitive ocean island basalts by crustal gabbro assimilation and multiple recharge of plume-derived melts

    NASA Astrophysics Data System (ADS)

    Borisova, Anastassia Y.; Bohrson, Wendy A.; Grégoire, Michel

    2017-07-01

    Chemical Geodynamics relies on a paradigm that the isotopic composition of ocean island basalt (OIB) represents equilibrium with its primary mantle sources. However, the discovery of huge isotopic heterogeneity within olivine-hosted melt inclusions in primitive basalts from Kerguelen, Iceland, Hawaii and South Pacific Polynesia islands implies open-system behavior of OIBs, where during magma residence and transport, basaltic melts are contaminated by surrounding lithosphere. To constrain the processes of crustal assimilation by OIBs, we employed the Magma Chamber Simulator (MCS), an energy-constrained thermodynamic model of recharge, assimilation and fractional crystallization. For a case study of the 21-19 Ma basaltic series, the most primitive series ever found among the Kerguelen OIBs, we performed sixty-seven simulations in the pressure range from 0.2 to 1.0 GPa using compositions of olivine-hosted melt inclusions as parental magmas, and metagabbro xenoliths from the Kerguelen Archipelago as wallrock. MCS modeling requires that the assimilant is anatectic crustal melts (P2O5 ≤ 0.4 wt.% contents) derived from the Kerguelen oceanic metagabbro wallrock. To best fit the phenocryst assemblage observed in the investigated basaltic series, recharge of relatively large masses of hydrous primitive basaltic melts (H2O = 2-3 wt%; MgO = 7-10 wt.%) into a middle crustal chamber at 0.2 to 0.3 GPa is required. Our results thus highlight the important impact that crustal gabbro assimilation and mantle recharge can have on the geochemistry of mantle-derived olivine-phyric OIBs. The importance of crustal assimilation affecting primitive plume-derived basaltic melts underscores that isotopic and chemical equilibrium between ocean island basalts and associated deep plume mantle source(s) may be the exception rather than the rule.

  11. Temperature and composition dependencies of trace element partitioning - Olivine/melt and low-Ca pyroxene/melt

    NASA Technical Reports Server (NTRS)

    Colson, R. O.; Mckay, G. A.; Taylor, L. A.

    1988-01-01

    This paper presents a systematic thermodynamic analysis of the effects of temperature and composition on olivine/melt and low-Ca pyroxene/melt partitioning. Experiments were conducted in several synthetic basalts with a wide range of Fe/Mg, determining partition coefficients for Eu, Ca, Mn, Fe, Ni, Sm, Cd, Y, Yb, Sc, Al, Zr, and Ti and modeling accurately the changes in free energy for trace element exchange between crystal and melt as functions of the trace element size and charge. On the basis of this model, partition coefficients for olivine/melt and low-Ca pyroxene/melt can be predicted for a wide range of elements over a variety of basaltic bulk compositions and temperatures. Moreover, variations in partition coeffeicients during crystallization or melting can be modeled on the basis of changes in temperature and major element chemistry.

  12. Al-augite and Cr-diopside ultramafic xenoliths in basaltic rocks from western United States

    USGS Publications Warehouse

    Wilshire, H.G.; Shervais, J.W.

    1975-01-01

    Ultramafic xenoliths in basalts from the western United States are divided into Al-augite and Cr-diopside groups. The Al-augite group is characterized by Al, Ti-rich augites, comparatively Fe-rich olivine and orthopyroxene, and Al-rich spinel, the Cr-diopside group by Cr-rich clinopyroxene and spinel and by Mg-rich olivine and pyroxenes. Both groups have a wide range of subtypes, but the Al-augite group is dominated by augite-rich varieties, and the Cr-diopside group by olivine-rich lherzolites. ?? 1975.

  13. Petrological and Geochemical characterization of central Chihuahua basalts: a possible local sign of rifting activity

    NASA Astrophysics Data System (ADS)

    Espejel-Garcia, V. V.; Garcia-Rascon, M.; Villalobos-Aragon, A.; Morton-Bermea, O.

    2012-12-01

    The central part of the mexican state, Chihuahua, is the oriental border of the Sierra Madre Occidental (silicic large igneous province), which consist of series of ignimbrites divided into two volcanic groups of andesites and rhyolites. In the central region of Chihuahua, the volcanic rocks are now part of the Basin and Range, allowing the presence of mafic rocks in the lower areas. The study area is located approximately 200 km to the NW of Chihuahua city near to La Guajolota town, in the Namiquipa County. There are at least 5 outcrops of basalts to the west of the road, named Puerto de Lopez, Malpaises, El Tascate, Quebrada Honda, and Carrizalio, respectively. These outcrops have only been previously described by the Mexican Geologic Survey (SGM) as thin basaltic flows, with vesicles filled with quartz, and phenocrystals of labradorite, andesine, oligoclase and olivine. Petrologically, the basalts present different textures, from small phenocrysts of plagioclase in a very fine matrix to large, zoned and sometimes broken phenocrysts of plagioclase in a coarser matrix. All samples have olivine in an advanced state of alteration, iddingsite. The geochemical analyses report that these basaltic flows contain characteristics of rift basalts. The rocks have a normative olivine values from 5.78 to 27.26 and nepheline values from 0 to 2.34. In the TAS diagram the samples straddle the join between basalt and trachy-basalt, reflecting a high K2O content. The Mg# average is 0.297, a value that suggests that the basalts do not come from a primitive magma. The basalts have high values of Ba (945-1334 ppm), Cu (54-147 ppm), and Zn (123-615 ppm). The contents of Rb (23-57 ppm), Sr (659-810 ppm), Y (26-33 ppm), Zr (148-217 ppm) and Cr (79-98 ppm) are characteristics of rift basalts. Using discrimination diagrams, the basalts plot in the field of within plate, supporting the rifting origin. Outcrops of other basalts, at about 80 to 100 km to the east of the study area, Lomas El

  14. Cr, Mn, and Ca distributions for olivine in angritic systems: Constraints on the origins of Cr-rich and Ca-poor core olivine in angrite LEW87051

    NASA Technical Reports Server (NTRS)

    Mikouchi, T.; Mckay, G.; Le, L.

    1994-01-01

    Angrite meteorites are a type of basaltic achondrites that are noted for their very old cyrstallization ages (4.55 b.y.) and unusual chemical and mineralogical properties. In spite of great interest, only four angrites have been found. LEW87051 is the smallest one which weighs 0.6 g. It is a porphyritic rock with coarse subhedral to euhedral olivines set in a fine-grained groundmass which clearly represents a crystallized melt. The largest uncertainty about the petrogenesis of LEW87051 is the relationship between the large olivine crystals and the groundmass. Prinz et al. suggests that olivines are xenocrysts, while McKay et al. proposed a fractional cyrstallization model based on experimental studies. However, the crystals have Cr-rich and Ca-poor cores which do not match experimental olivines. Although Jurewicz and McKay tried to explaine the zoning of the rim by diffusion, some features are not explained. There also exists a definite composition boundary of Fe(2+) and MnO between the core and the rim. To clarify the origin of these olivines, we have performed experiments using LEW87051 analogs to measure the effects of oxygen fugacity on distribution coefficients of various elements in an angritic system.

  15. Olivine and chromian spinel in primitive calc-alkaline and tholeiitic lavas from the southernmost cascade range, California: A reflection of relative fertility of the source

    USGS Publications Warehouse

    Clynne, M.A.; Borg, L.E.

    1997-01-01

    Chromian spinel and coexisting olivine phenocrysts from a geochemically diverse suite of primitive tholeiitic and calc-alkaline basalts and magnesian andesites from the Lassen region, in the southernmost Cascade Range, in California, show that the sub-arc mantle is zoned. Depleted calc-alkaline basalts and magnesian andesites erupt in the forearc region, and calc-alkaline basalts contain increasing abundances of incompatible elements toward the backarc. High-alumina olivine tholeiites erupt from the arc and backarc areas. Olivine from all these lavas displays a limited compositional range, from Fo86 to Fo91, and crystallized at high temperature, generally 1225-1275??C. Chromian spinel trapped in the olivine phenocrysts displays a large range of composition: Cr# values span the range 9-76. Excess Al in the spinel relative to that in 1-atm spinel suggests that it crystallized at elevated pressure. The phenocrysts in these lavas are in equilibrium with their host liquids. The full range of Cr# of the spinel compositions cannot be explained by differentiation or variable pressure, variations in f(O2), subsolidus equilibration or variations in degree of partial melting of a single peridotitic source. Rather, the systematic compositional differences among phenocrysts in these primitive lavas result from bulk chemical variability in their mantle sources. Correlations between spinel and host-rock compositions support the assertion that the geochemical diversity of Lassen basalts reflects the relative fertility of their mantle sources.

  16. Rhyolite, dacite, andesite, basaltic andesite, and basalt volcanism on the Alarcon Rise spreading-center, Gulf of California

    NASA Astrophysics Data System (ADS)

    Dreyer, B. M.; Portner, R. A.; Clague, D. A.; Castillo, P. R.; Paduan, J. B.; Martin, J. F.

    2012-12-01

    The Alarcon Rise is a ~50 km long intermediate-rate (~50mm/a) spreading segment at the southern end of the Gulf of California. The Rise is bounded by the Tamayo and Pescadero transforms to the south and north. In Spring 2012, an MBARI-led expedition mapped a ~1.5- 3km wide swath of the ridge axis at 1-m resolution and completed 9 ROV dives (Clague et al., this session). Sampling during the ROV dives was supplemented by use of a wax-tip corer to recover volcanic glass: 194 glassy lava samples were recovered from the Rise. The vast majority of lava flows along the axis are basalt and rare basaltic andesite. More than half the basalts are plagioclase-phyric to ultraphyric (Martin et al., this session), and the rest are aphyric. Rare samples also include olivine or olivine and clinopyroxene phenocrysts. Analyses of half of the recovered glass basalt rinds range in MgO from 4.3 to 8.5 wt.% and those with MgO > 6 wt % have K2O/TiO2 = 0.07-0.11. The basalts are broadly characterized as normal mid-ocean ridge basalts (N-MORB). E-MORB is also present near the center of the ridge segment, but has been found only as pyroclasts in sediment cores. A much greater range in lava composition is associated with an unusual volcanic dome-like edifice that lies ~9 km south of the Pescadero transform. Two dives in the vicinity of the dome collected lava and volcaniclastic samples consisting of moderately to sparsely phyric light brown to colorless volcanic glass. Feldspar is the dominant phase, but magnetite, fayalitic olivine, light tan and light green clinopyroxene, orthopyroxene, zircon, and rare pyrite blebs also occur. Melt-inclusions are common in many phenocrysts, especially of plagioclase. Hydrous mineral phases are not observed. These samples have rhyolitic glass compositions (75.8- 77.4 SiO2 wt %), but their whole-rock compositions will be somewhat less silicic. Pillow flows to the immediate west have dacitic glass compositions (67.4- 68.8 wt % SiO2). Basaltic andesitic

  17. Chromium Oxidation State in Planetary Basalts: Oxygen Fugacity Indicator and Critical Variable for Cr-Spinel Stability

    NASA Technical Reports Server (NTRS)

    Bell, A. S.; Burger, P. V.; Le, Loan; Papike, J. J.; Jone, J.; Shearer, C. K.

    2014-01-01

    Cr is a ubiquitous and relatively abundant minor element in basaltic, planetary magmas. At the reduced oxidation states (basalts Cr is present in melts as both divalent and trivalent forms. The ratio of trivalent to divalent Cr present in the melt has many consequences for the stability and Cr concentration of magmatic phases such as spinel, clinopyroxene, and olivine. However, understanding the Cr valence in quenched melts has historically been plagued with analytical issues, and only recently has reliable methodology for quantifying Cr valence in quenched melts been developed. Despite this substantial difficulty, the pioneering works of Hanson and Jones and Berry and O'Neill provided important insights into the oxidation state of Cr in in silicate melts. Here we present a series of 1-bar gas mixing experiments performed with a Fe-rich basaltic melt in which have determined the Cr redox ratio of the melt at over a range of fO2 values by measuring this quantity in olivine with X-ray Absorption Near Edge Spectroscopy (XANES). The measured Cr redox ratio of the olivine phenocrysts can be readily converted to the ratio present in the conjugate melt via the ratio of crystal-liquid partition coefficients for Cr3+ and Cr2+. We have applied these results to modeling Cr spinel stability and Cr redox ratios in a primitive, iron-rich martian basalt.

  18. An analysis of Apollo lunar soil samples 12070,889, 12030,187, and 12070,891: Basaltic diversity at the Apollo 12 landing site and implications for classification of small-sized lunar samples

    NASA Astrophysics Data System (ADS)

    Alexander, Louise; Snape, Joshua F.; Joy, Katherine H.; Downes, Hilary; Crawford, Ian A.

    2016-09-01

    Lunar mare basalts provide insights into the compositional diversity of the Moon's interior. Basalt fragments from the lunar regolith can potentially sample lava flows from regions of the Moon not previously visited, thus, increasing our understanding of lunar geological evolution. As part of a study of basaltic diversity at the Apollo 12 landing site, detailed petrological and geochemical data are provided here for 13 basaltic chips. In addition to bulk chemistry, we have analyzed the major, minor, and trace element chemistry of mineral phases which highlight differences between basalt groups. Where samples contain olivine, the equilibrium parent melt magnesium number (Mg#; atomic Mg/[Mg + Fe]) can be calculated to estimate parent melt composition. Ilmenite and plagioclase chemistry can also determine differences between basalt groups. We conclude that samples of approximately 1-2 mm in size can be categorized provided that appropriate mineral phases (olivine, plagioclase, and ilmenite) are present. Where samples are fine-grained (grain size <0.3 mm), a "paired samples t-test" can provide a statistical comparison between a particular sample and known lunar basalts. Of the fragments analyzed here, three are found to belong to each of the previously identified olivine and ilmenite basalt suites, four to the pigeonite basalt suite, one is an olivine cumulate, and two could not be categorized because of their coarse grain sizes and lack of appropriate mineral phases. Our approach introduces methods that can be used to investigate small sample sizes (i.e., fines) from future sample return missions to investigate lava flow diversity and petrological significance.

  19. Olivine-rich asteroids in the near-Earth space

    NASA Astrophysics Data System (ADS)

    Popescu, Marcel; Perna, D.; Barucci, M. A.; Fornasier, S.; Doressoundiram, A.; Lantz, C.; Merlin, F.; Belskaya, I. N.; Fulchignoni, M.

    2018-06-01

    In the framework of a 30-night spectroscopic survey of small near-Earth asteroids (NEAs), we present new results regarding the identification of olivine-rich objects. The following NEAs were classified as A-type using visible spectra obtained with 3.6-m New Technology Telescope: (293726) 2007 RQ17, (444584) 2006 UK, 2012 NP, 2014 YS34, 2015 HB117, 2015 LH, 2015 TB179, 2015 TW144. We determined a relative abundance of 5.4 per cent (8 out of 147 observed targets) A-types at a 100-m size range of NEA population. The ratio is at least five times larger compared with the previously known A-types, which represent less than ˜ 1 per cent of NEAs taxonomically classified. By taking into account that part of our targets may not be confirmed as olivine-rich asteroids by their near-infrared spectra, or they can have a nebular origin, our result provides an upper-limit estimation of mantle fragments at size ranges below 300 m. Our findings are compared with the `battered-to-bits' scenario, claiming that at small sizes the olivine-rich objects should be more abundant when compared with basaltic and iron ones.

  20. 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.

  1. NanoSIMS results from olivine-hosted melt embayments: Magma ascent rate during explosive basaltic eruptions

    NASA Astrophysics Data System (ADS)

    Lloyd, Alexander S.; Ruprecht, Philipp; Hauri, Erik H.; Rose, William; Gonnermann, Helge M.; Plank, Terry

    2014-08-01

    The explosivity of volcanic eruptions is governed in part by the rate at which magma ascends and degasses. Because the time scales of eruptive processes can be exceptionally fast relative to standard geochronometers, magma ascent rate remains difficult to quantify. Here we use as a chronometer concentration gradients of volatile species along open melt embayments within olivine crystals. Continuous degassing of the external melt during magma ascent results in diffusion of volatile species from embayment interiors to the bubble located at their outlets. The novel aspect of this study is the measurement of concentration gradients in five volatile elements (CO2, H2O, S, Cl, F) at fine-scale (5-10 μm) using the NanoSIMS. The wide range in diffusivity and solubility of these different volatiles provides multiple constraints on ascent timescales over a range of depths. We focus on four 100-200 μm, olivine-hosted embayments erupted on October 17, 1974 during the sub-Plinian eruption of Volcán de Fuego. H2O, CO2, and S all decrease toward the embayment outlet bubble, while F and Cl increase or remain roughly constant. Compared to an extensive melt inclusion suite from the same day of the eruption, the embayments have lost both H2O and CO2 throughout the entire length of the embayment. We fit the profiles with a 1-D numerical diffusion model that allows varying diffusivities and external melt concentrations as a function of pressure. Assuming a constant decompression rate from the magma storage region at approximately 220 MPa to the surface, H2O, CO2 and S profiles for all embayments can be fit with a relatively narrow range in decompression rates of 0.3-0.5 MPa/s, equivalent to 11-17 m/s ascent velocity and an 8 to 12 minute duration of magma ascent from ~ 10 km depth. A two stage decompression model takes advantage of the different depth ranges over which CO2 and H2O degas, and produces good fits given an initial stage of slow decompression (0.05-0.3 MPa/s) at high

  2. Volcanic diapirs in the Orange Mountain flood basalt: New Jersey, USA

    NASA Astrophysics Data System (ADS)

    Puffer, John H.; Laskowich, Chris

    2012-09-01

    Diapir-shaped structures, 4-30 m high, consisting of vesicular basalt have intruded into the interior of a 50-70 m-thick subaerial Orange Mountain Basalt flow exposed at several rock quarries in northern New Jersey. The basalt flowed onto a travertine encrusted mudflat saturated with alkali salts. We propose that pressurized alkali vapors trapped under the lava created a vesicular and viscous flow bottom layer about 10 m thick. Vesicle coalescence within this layer increased its buoyancy where it locally accumulated into diapirs and displaced overlying lava. Large bubbles within the diapirs expanded upon intrusion into hot flow interiors where they explosively escaped leaving lenses of breccia. Some early diapirs reached the base of the upper lava crust. These diapirs document vapor driven convection of large blobs of contaminated lava into the lava core of the Orange Mountain flow.

  3. High alumina (HA) and very high potassium (VHK) basalt clasts from Apollo 14 breccias. I - Mineralogy and Petrology - Evidence of crystallization from evolving magmas

    NASA Technical Reports Server (NTRS)

    Neal, C. R.; Taylor, L. A.; Patchen, A. D.

    1989-01-01

    The mineralogy and petrography of very high potassium (VHK) and high alumina (HA) basalts from the Apollo 14 site provide an insight into their magmatic evolution. Generally, their parageneses are similar, with olivine and chromite the early liquidus phases, followed by plagioclase and pyroxene, which crystallized together. Although late-stage ilmenite and FeNi metal occur in both VHK and HA samples, the VHKs also crystallize K-feldspar and Fa-rich olivine. Zoning of constituent minerals is similar for both basalt types, demonstrating that the parental magmas for both HA and VHK basalts became enriched in K, Na, Ca, Fe, and Ti and depleted in Mg and Al as crystallization proceeded. Enrichment of K in the VHK basalts is above that expected from normal fractional crystallization.

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

    NASA Astrophysics Data System (ADS)

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

    2010-11-01

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

  5. Ibitira: A basaltic achondrite from a distinct parent asteroid

    NASA Technical Reports Server (NTRS)

    Mittlefehldt, David W.

    2004-01-01

    I have done detailed petrologic study of Ibitira, nominally classified as a basaltic eucrite. The Fe/Mn ratio of Ibitira pyroxenes with <10 mole % wollastonite component is 36.4 0.4, and is well-resolved from those of five basaltic eucrites studied for comparison; 31.2-32.2. Data for the latter completely overlap. Ibitira pyroxenes have lower Fe/Mg than the basaltic eucrite pyroxenes. Thus, the higher Fe/Mn ratio does not reflect a simple difference in oxidation state. Ibitira also has an oxygen isotopic composition, alkali element contents and a Ti/Hf ratio that distinguish it from basaltic eucrites. These differences support derivation from a distinct parent asteroid. Ibitira is the first recognized representative of the fifth known asteroidal basaltic crust.

  6. Giant Plagioclase "Mosaicrysts" and Other Textures in the Steens Basalt, Columbia River Flood Basalt Province

    NASA Astrophysics Data System (ADS)

    Grunder, A.; Moore, N. E.; Bohrson, W. A.

    2015-12-01

    The Steens Basalts (~16.7 Ma), the oldest and most mafic stage of Columbia River flood basalt volcanism, are known for lavas with conspicuous giant plagioclase laths (2 - 5 cm in diameter). Such flows are intercalated with ones that are nearly aphyric or that bear plagioclase (plag) phenocrysts of 0.5-2 cm. Addition textures are distinctive radial, snowflake plag clusters and sandwich glomerocrysts of plag, with olivine trapped between laths. These clusters and glomerocrysts are typically 1, but as large as 3 cm in diameter. Plag composition of all textural types is limited (An76-60). Plag dominates the phenocryst mode; rare flows, mainly low in the section, have olivine > plag and phenocrystic clinopyroxene occurs rarely, and mainly high in the section. Unlike the flows, dikes have few phenocrysts; giant laths are rare and the snowflake texture has not been observed. Giant plag laths are euhedral and make up a few percent to more than 50% of the rock. Many plag megacrysts are made of several plag crystals that form a mosaic, where the constituent crystals are crystallographically distinct and are overgrown with feldspar to make the crystal euhedral. We describe these composite megacrysts as "mosaicrysts". We are exploring magmatic conditions that would trigger oversaturation to spawn rapid growth yielding clusters and overgrowths that form mosaicrysts. Giant plagioclase basalts (so-called GPB) are also described for the Deccan and Emeishan flood basalt provinces attesting to similar magmatic processes. Plag laths typically define strong flow foliation at the flow base, have a swirled distribution in the flow core, and are sparse in the top. Some particularly crystal-rich flows (or sills) have an abrupt transition to a crystal-poor upper few decimeters of the several-m- thick flow. We interpret the crystal-poor top to be the expelled melt from crystal accumulation in the flow, which locally reinjects and is entrained in lower crystal mush.

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

    PubMed

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

    2016-09-29

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

  8. 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

  9. Failed Silurian continental rifting at the NW margin of Gondwana: evidence from basaltic volcanism of the Prague Basin (Teplá-Barrandian Unit, Bohemian Massif)

    NASA Astrophysics Data System (ADS)

    Tasáryová, Zuzana; Janoušek, Vojtěch; Frýda, Jiří

    2018-06-01

    The Silurian volcanic rocks of the Prague Basin represent within-plate, transitional alkali to tholeiitic basalts, which erupted in a continental rift setting through the thick Cadomian crust of the Teplá-Barrandian Unit (Bohemian Massif). Despite the variable, often intense alteration resulting in post-magmatic replacement of the basalt mass due to carbonatization, the geochemical signatures of Silurian basalts are still sufficiently preserved to constrain primary magmatic processes and geotectonic setting. The studied interval of Silurian volcanic activity ranges from Wenlock (Homerian, 431 Ma) to late Ludlow (Gorstian, 425 Ma) with a distinct peak at the Wenlock/Ludlow boundary ( 428 Ma). Trace-element characteristics unambiguously indicate partial melting of a garnet peridotite mantle source. Wenlock basalts are similar to alkaline OIB with depleted radiogenic Nd signature compared to Ludlow basalts, which are rather tholeiitic, EMORB-like with enriched radiogenic Nd signature. The correlation of petrogenetically significant trace-element ratios with Nd isotopic compositions points to a mixing of partial melts of an isotopically heterogeneous, possibly two-component mantle source during the Wenlock-Ludlow melting. Lava eruptions were accompanied by intrusions of doleritic basalt and meimechite sills. The latter represent olivine-rich cumulates of basaltic magmas of probably predominantly Ludlow age. Meimechites with dolerites and, to a lesser extent, some lavas were subject to alteration due to wall-rock-fluid interaction. The trigger for the Wenlock-to-Ludlow (431-425 Ma) extension and related volcanism in the Prague Basin is related to far-field forces, namely slab-pull regime due to progressive closure of the Iapetus Ocean. The main stage of the Baltica-Laurentia collision then caused the Prague Basin rift failure at ca. 425 Ma that has never reached an oceanic stage.

  10. Olivines and olivine coronas in mesosiderites

    NASA Technical Reports Server (NTRS)

    Nehru, C. E.; Zucker, S. M.; Harlow, G. E.; Prinz, M.

    1980-01-01

    The paper presents a study of olivines and their surrounding coronas in mesosiderites texturally and compositionally using optical and microprobe methods. Olivine composition ranges from Fo(58-92) and shows no consistent pattern of distribution within and between mesosiderites; olivine occurs as large single crystals or as partially recrystallized mineral clasts, except for two lithic clasts. These are Emery and Vaca Muerta, and both are shock-modified olivine orthopyroxenites. Fine-grained coronas surround olivine, except for those in impact-melt group mesosiderites and those without tridymite in their matrices. Coronas consist largely of orthopyroxene, plagioclase, clinopyroxene, chromite, merillite, and ilmenite, and are similar to the matrix, but lack metal and tridymite. Texturally the innermost parts of the corona can be divided into three stages of development: (1) radiating acicular, (2) intermediate, and (3) granular.

  11. Lunar basalt meteorite EET 87521: Petrology of the clast population

    NASA Technical Reports Server (NTRS)

    Semenova, A. S.; Nazarov, M. A.; Kononkova, N. N.

    1993-01-01

    The Elephant Moraine meteorite EET 87521 was classified as a lunar mare basalt breccia which is composed mainly of VLT basalt clasts. Here we report on our petrological study of lithic clasts and monomineralic fragments in the thin sections EET 87521,54 and EET 87521,47,1, which were prepared from the meteorite. The results of the study show that EET 87521 consists mainly of Al-rich ferrobasalt clasts and olivine pyroxenite clasts. The bulk composition of the meteorite can be well modelled by the mixing of these lithic components which appear to be differentiates of the Luna 25 basalt melt. KREEP and Mg-rich gabbro components are minor constituents of EET 87521.

  12. Thermodynamic assessment of the magmatic history of Blue Rock shield volcano, Jackson Co., Oregon: application of a new DNi (olivine-melt) geothermometer and other models

    NASA Astrophysics Data System (ADS)

    Crabtree, Stephen M.; Huber, Abigail; Beck, Karl

    2017-05-01

    Blue Rock is a basaltic shield volcano in the southern Oregon Cascades, north of Mt. McLoughlin, showing bulk phenocryst abundances ranging from 5 to 28 vol%, and a variety of groundmass textures. Compositional analyses of olivine and plagioclase phenocrysts and glomerocrysts allowed for the sequential application of a new {D}_{Ni}^{olivine-melt} thermometer, a plagioclase-melt hygrometer, and a viscosity model to define olivine-in conditions for a suite of lavas erupted from this edifice. Calculated olivine-in temperatures were compared to results from the anhydrous MELTS model, and the D (Mg) model of Beattie (1993). Model results were consistent with experimental data for hydrous arc basalts with respect to temperature (1053-1146 °C), dissolved-H2O contents (0.9-2.4 wt% H2O), and viscosity (1.9-2.2 log10 Pa s), confirming the utility of these models in assessing the thermodynamic properties of mafic, hydrous arc lavas over a broad range in crystallinity, requiring only the completion of bulk geochemical and microprobe analyses. These studies also reinforced the significant and predictable role of water, affecting the compositions of crystals grown during magmatic ascent, and allowed the definition of a reasonable multi-stage eruptive sequence consistent with the degassing of magmas on ascent in the formation of this small-scale basaltic edifice.

  13. Relation of the spectroscopic reflectance of olivine to mineral chemistry and some remote sensing implications

    NASA Technical Reports Server (NTRS)

    King, Trude V. V.; Ridley, W. Ian

    1987-01-01

    High-resolution visible and near-IR diffuse spectral reflectance are used to systematically investigate apparent wavelength shifts as a function of mineral chemistry in the Fe/Mg olivine series from Fo(11) to Fo(91). The study also shows that trace amounts of nickel can be spectrally detected in the olivine structure. Significant compositional information can only be extracted at relatively high resolution, because the overall spectral characteristics of the olivines change only subtly as a function of the Fe/Mg ratio. This laboratory study is expected to aid in the interpretation of remotely sensed data from both terrestrial and extraterrestrial bodies. Terrestrial applications may include the recognition of ultramafic, ultrabasic, and basaltic terrains which in themselves may have mineral potential. Among extraterrestrial applications, the asteroids are obvious candidates for further examination. Some permutations of Fe-Mg-Ni relations in olivines are discussed as they apply to the interpretation of asteroid surfaces and other extraterrestrial bodies.

  14. Comparative Planetary Mineralogy: Co, Ni Systematics in Chromite from Planetary Basalts

    NASA Technical Reports Server (NTRS)

    Karner, J. M.; Shearer, C. K.; Papike, J. J.; Righter,K.

    2005-01-01

    Spinel is a minor but important phase in planetary basalts because its variable composition often reflects basalt petrogenesis. For example, complicated zoning trends in spinel can give clues to melt evolution [1], and V concentrations in chromite lend insight into magma oxygen fugacity (fO2) conditions [2]. Nickel and Co are two elements that are commonly used as a measure of melt fractionation, and their partitioning between olivine and melt is fairly well understood. Less clear is their partitioning into spinel, although [3] has explored Ni and Co systematics in experimental charges. This study documents Ni and Co behavior in early crystallizing spinel (chromite) from several planetary basalts in an attempt to compare our results with [3], and also gain insight into basalt evolution on the three planets.

  15. Olivine-respiring bacteria isolated from the rock-ice interface in a lava-tube cave, a Mars analog environment.

    PubMed

    Popa, Radu; Smith, Amy R; Popa, Rodica; Boone, Jane; Fisk, Martin

    2012-01-01

    The boundary between ice and basalt on Earth is an analogue for some near-surface environments of Mars. We investigated neutrophilic iron-oxidizing microorganisms from the basalt-ice interface in a lava tube from the Oregon Cascades with perennial ice. One of the isolates (Pseudomonas sp. HerB) can use ferrous iron Fe(II) from the igneous mineral olivine as an electron donor and O(2) as an electron acceptor. The optimum growth temperature is ∼12-14°C, but growth also occurs at 5°C. Bicarbonate is a facultative source of carbon. Growth of Pseudomonas sp. HerB as a chemolithotrophic iron oxidizer with olivine as the source of energy is favored in low O(2) conditions (e.g., 1.6% O(2)). Most likely, microbial oxidation of olivine near pH 7 requires low O(2) to offset the abiotic oxidation of iron. The metabolic capabilities of this bacterium would allow it to live in near-surface, icy, volcanic environments of Mars in the present or recent geological past and make this type of physiology a prime candidate in the search for life on Mars.

  16. Petrogenesis of Mare Basalts, Mg-Rich Suites and SNC Parent Magmas

    NASA Technical Reports Server (NTRS)

    Hess, Paul C.

    2004-01-01

    The successful models for the internal evolution of the Moon must consider the volume, distribution, timing, composition and, ultimately, the petrogenesis of mare basaltic volcanism. Indeed, given the paucity of geophysical data, the internal state of the Moon in the past can be gleaned only be unraveling the petrogenesis of the various igneous products on the Moon and, particularly, the mare basalts. most useful in constraining the depth and composition of their source region [Delano, 1980] despite having undergone a certain degree of shallow level olivine crystallization.The bulk of the lunar volcanic glass suite can be modeled as the partial melting products of an olivine + orthopyroxene source region deep within the lunar mantle. Ti02 contents vary from 0.2 wt % -1 7.0wt [Shearer and Papike, 1993]. Values that extreme would seem to require a Ti- bearing phase such as ilmenite in the source of the high-Ti (but not in the VLT source) because a source region of primitive LMO olivine and orthopyroxene, even when melted in small degrees cannot account for the observed range of Ti02 compositions. The picritic glasses are undersaturated with respect to ilmenite at all pressures investigated therefore ilmenite must have been consumed during melting, leaving an ilmenite free residue and an undersaturated melt [Delano, 1980, Longhi, 1992, Elkins et al, 2000 among others]. Multi- saturation pressures for the glasses potentially represent the last depths at which the liquids equilibrated with a harzburgite residue before ascending to the surface. These occur at great depths within the lunar mantle. Because the liquids have suffered some amount of crystal fractionation, this is at best a minimum depth. If the melts are mixtures, then it is only an average depth of melting. Multisaturation, nevertheless, is still a strong constraint on source mineralogy, revealing that the generation of the lunar basalts was dominated by melting of olivine and orthopyroxene.

  17. Exploration of H2O-CO2 Solubility in Alkali Basalt at low-H2O

    NASA Astrophysics Data System (ADS)

    Roggensack, K.; Allison, C. M.; Clarke, A. B.

    2017-12-01

    A number of recent experimental studies have found conflicting evidence for and against the influence of H2O on CO2 solubility in basalt and alkali-rich mafic magma (e.g. Behrens et al., 2009; Shishkina et al., 2010;2014; Iacono-Marziano et al., 2012). Some of the uncertainty is due to the error with spectroscopic determination (FTIR) of carbon and the challenge of controlling H2O abundance in experiments. It's been widely observed that even experimental capsules without added H2O may produce hydrous glasses containing several wt.% H2O. We conducted fluid-saturated, mixed-fluid (H2O-CO2) experiments to determine the solubility in alkali basalt with particular emphasis on conditions at low-H2O. To limit possible H2O contamination, materials were dried prior to loading and experimental capsules were sealed under vacuum. Experiments were run using a piston-cylinder, in Pt (pre-soaked in Fe) or AuPd capsules and operating at pressures from 400 to 600 MPa. Post-run the capsules were punctured under vacuum and fluids were condensed, separated, and measured by mercury manometry. A comparison between two experiments run at the same temperature and pressure conditions but with different fluid compositions illustrates the correlation between carbonate and H2O solubility. Uncertainties associated with using concentrations calculated from FTIR data can be reduced by directly comparing analyses on wafers of similar thickness. We observe that the experiment with greater H2O absorbance also has a higher carbonate absorbance than the experiment with lower H2O absorbance. Since the experiments were run at the same pressure, the experiment with more water-rich fluid, and higher dissolved H2O, has lower CO2 fugacity, but surprisingly has higher dissolved CO2 content. Overall, the results show two distinct trends. Experiments conducted at low-H2O (0.5 to 0.8 wt.%) show lower dissolved CO2 than those conducted at moderate-H2O (2 to 3 wt.%) at similar CO2 fugacity. These data show that

  18. 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

  19. 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.

  20. Geobarometry of ultramafic xenoliths from Loihi Seamount, Hawaii, on the basis of CO2 inclusions in olivine

    USGS Publications Warehouse

    Roedder, E.

    1983-01-01

    Abundant fluid inclusions in olivine of dunite xenoliths (???1-3 cm) in basalt dredged from the young Loihi Seamount, 30 km southeast of Hawaii, are evidence for three coexisting immiscible fluid phases-silicate melt (now glass), sulfide melt (now solid), and dense supercritical CO2 (now liquid + gas)-during growth and later fracturing of some of these olivine crystals. Some olivine xenocrysts, probably from disaggregation of xenoliths, contain similar inclusions. Most of the inclusions (2-10 ??m) are on secondary planes, trapped during healing of fractures after the original crystal growth. Some such planes end abruptly within single crystals and are termed pseudosecondary, because they formed during the growth of the host olivine crystals. The "vapor" bubble in a few large (20-60 ??m), isolated, and hence primary, silicate melt inclusions is too large to be the result of simple differential shrinkage. Under correct viewing conditions, these bubbles are seen to consist of CO2 liquid and gas, with an aggregate ??{variant} = ??? 0.5-0.75 g cm-3, and represent trapped globules of dense supercritical CO2 (i.e., incipient "vesiculation" at depth). Some spinel crystals enclosed within olivine have attached CO2 blebs. Spherical sulfide blebs having widely variable volume ratios to CO2 and silicate glass are found in both primary and pseudosecondary inclusions, demonstrating that an immiscible sulfide melt was also present. Assuming olivine growth at ??? 1200??C and hydrostatic pressure from a liquid lava column, extrapolation of CO2 P-V-T data indicates that the primary inclusions were trapped at ??? 220-470 MPa (2200-4700 bars), or ??? 8-17 km depth in basalt magma of ??{variant} = 2.7 g cm-3. Because the temperature cannot change much during the rise to eruption, the range of CO2 densities reveals the change in pressure from that during original olivine growth to later deformation and rise to eruption on the sea floor. The presence of numerous decrepitated inclusions

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

    NASA Astrophysics Data System (ADS)

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

    2018-06-01

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

  2. Mineralogy and geochemistry of picro-dolerite dykes from the central Deccan Traps flood basaltic province, India, and their geodynamic significance

    NASA Astrophysics Data System (ADS)

    Dongre, Ashish; Viljoen, K. S.; Rathod, A.

    2018-04-01

    Constituent mineral compositions and whole rock major element geochemistry of picro-dolerite dykes from the central part of the Deccan flood basalt province are presented and discussed. The dykes are characterized by an MgO content of about 13 wt%, coupled with 13-16 modal percents of olivine. A high whole rock molar Mg# value of 71 and the presence of magnesian olivine phenocrysts ( Fo78) are consistent with a primitive (i.e. unevolved) geochemistry. The nature and composition of clinopyroxene (augite and pigeonite), plagioclase feldspar (labradorite) and Fe-Ti oxides (mostly ilmenite and magnetite) are also discussed, with implications drawn with respect to the geodynamics. High MgO magmas and rocks such as picrites are generally considered to be indicative of plume magmatism, formed by high degrees of partial melting in, e.g. the high-temperature region of a plume head. Recent age data is consistent with a model in which the Deccan LIP picritic magmatism is associated with the main phase of Deccan Trap activity at 66 Ma, as a result of a syn- to post rifting phase associated with the impact of the Rèunion mantle plume. It is speculated that the differentiation of primary olivine basaltic magma of picritic composition, may have been the mechanism for the generation of alkalic basalts which occurs in the Deccan Trap basaltic sequence.

  3. Geochemical stratigraphy of lava flows sampled by the Hawaii Scientific Drilling Project

    NASA Astrophysics Data System (ADS)

    Rhodes, J. M.

    1996-05-01

    Geochemical discriminants are used to place the boundary between Mauna Loa flows and underlying Mauna Kea flows at a depth of about 280 m. At a given MgO content the Mauna Kea flows are lower in SiO2 and total iron and higher in total alkali, TiO2, and incompatible elements than the Mauna Loa lavas. The uppermost Mauna Kea lavas (280 to 340 m) contain alkali basalts interlayered with tholeiites and correlate with the postshield Hamakua Volcanics. In addition to total alkalis, the alkali basalts have higher TiO2, P2O5, Sr, Ba, Ce, La, Zr, Nb, Y, and V relative to the tholeiites and lower Zr/Nb and Sr/Nb ratios. Some of the alkali basalts are extensively differentiated. Below 340 m all the flows are tholeiitic, with compositions broadly similar to the few "fresh" subaerial shield-building Mauna Kea tholeiites studied to date. High-MgO lavas are unusually abundant, although there is a wide range (7-28%) in MgO content reflecting olivine control. FeO/MgO relationships are used to infer parental picritic magmas with about 15 wt % MgO. Lavas with more MgO than this have accumulated olivine. The Mauna Loa lavas have compositional trends that are controlled by olivine crystallization and accumulation. They compare closely with trends for historical (1843-1984) flows, tending toward the depleted end of the spectrum. They are, though, much more MgO-rich (9-30%) than is typical for most historical and young (<30 ka) prehistoric lavas. The unusual abundance of high-MgO and picritic lavas is attributed to the likelihood that only large-volume, hot, mobile flows will reach Hilo Bay from the northeast rift zone. FeO/MgO relationships are used to infer parental picritic magmas with about 17 wt % MgO. Again, lavas with more MgO than this have accumulated olivine. Systematic changes in incompatible element ratios are used to argue that the magma supply rate has diminished over time. On the other hand, the relatively constant Zr/Nb and Sr/Nb ratios that compare closely with

  4. Rock types of South Pole-Aitken basin and extent of basaltic volcanism

    USGS Publications Warehouse

    Pieters, C.M.; Head, J. W.; Gaddis, L.; Jolliff, B.; Duke, M.

    2001-01-01

    The enormous pre-Nectarian South Pole-Aitken (SPA) basin represents a geophysically and compositionally unique region on the Moon. We present and analyze the mineralogical diversity across this basin and discuss the implications for basin evolution. Rock types are derived from Clementine multispectral data based on diagnostic characteristics of ferrous absorptions in fresh materials. Individual areas are characterized as noritic (dominated by low-Ca pyroxene), gabbroic/basaltic (dominated by high-Ca pyroxene), feldspathic (<3-6% FeO), and olivine-gabbro (dominated by high-Ca pyroxene and olivine). The anorthositic crust has effectively been removed from the interior of the basin. The style of volcanism within the basin extends over several 100 Myr and includes mare basalt and pyroclastic deposits. Several areas of ancient (pre-Orientale) volcanism, or cryptomaria, have also been identified. The nonmare mafic lithology that occurs across the basin is shown to be noritic in composition and is pervasive laterally and vertically. We interpret this to represent impact melt/breccia deposits derived from the lower crust. A few localized areas are identified within the basin that contain more diverse lithologies (gabbro, olivine-gabbro), some of which may represent material from the deepest part of the lower crust and perhaps uppermost mantle involved in the SPA event. Copyright 2001 by the American Geophysical Union.

  5. Evidence from Olivine-Hosted Melt Inclusions that the Martian Mantle has a Chondritic D/H Ratio and that Some Young Basalts have Assimilated Old Crust

    NASA Technical Reports Server (NTRS)

    Usui, Tomohiro; Alexander, O'D.; Wang, J.; Simon, J. I.; Jones, J. H.

    2012-01-01

    Magmatic degassing of volatile elements affects the climate and near-surface environment of Mars. Telescopic and meteorite studies have revealed that the Martian atmosphere and near-surface materials have D/H ratios 5-6 times terrestrial values [e.g., 1, 2]. Such high D/H ratios are interpreted to result from the preferential loss of H relative to heavier D from the Martian atmosphere, assuming that the original Martian water inventory had a D/H ratio similar to terrestrial values and to H in primitive meteorites [e.g., 1, 3]. However, the primordial Martian D/H ratio has, until now, not been well constrained. The uncertainty over the Martian primordial D/H ratio has arisen both from the scarcity of primitive Martian meteorites and as a result of contamination by terrestrial and, perhaps, Martian surface waters that obscure the signature of the Martian mantle. This study reports a comprehensive dataset of magmatic volatiles and D/H ratios in Martian primary magmas based on low-contamination, in situ ion microprobe analyses of olivine-hosted melt inclusions from both depleted [Yamato 980459 (Y98)] and enriched [Larkman Nunatak 06319 (LAR06)] Martian basaltic meteorites. Analyses of these primitive melts provide definitive evidence that the Martian mantle has retained a primordial D/H ratio and that young Martian basalts have assimilated old Martian crust.

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

  7. Role of olivine cumulates in destabilizing the flanks of Hawaiian volcanoes

    USGS Publications Warehouse

    Clague, D.A.; Denlinger, R.P.

    1994-01-01

    The south flank of Kilauea Volcano is unstable and has the structure of a huge landslide; it is one of at least 17 enormous catastrophic landslides shed from the Hawaiian Islands. Mechanisms previously proposed for movement of the south flank invoke slip of the volcanic pile over seafloor sediments. Slip on a low friction de??collement alone cannot explain why the thickest and widest sector of the flank moves more rapidly than the rest, or why this section contains a 300 km3 aseismic volume above the seismically defined de??collement. It is proposed that this aseismic volume, adjacent to the caldera in the direction of flank slip, consists of olivine cumulates that creep outward, pushing the south flank seawards. Average primary Kilauea tholeiitic magma contains about 16.5 wt.% MgO compared with an average 10 wt.% MgO for erupted subaerial and submarine basalts. This difference requires fractionation of 17 wt.% (14 vol.%) olivine phenocrysts that accumulate near the base of the magma reservoir where they form cumulates. Submarine-erupted Kilauea lavas contain abundant deformed olivine xenocrysts derived from these cumulates. Deformed dunite formed during the tholeiitic shield stage is also erupted as xenoliths in subsequent alkalic lavas. The deformation structures in olivine xenocrysts suggest that the cumulus olivine was densely packed, probably with as little as 5-10 vol.% intercumulus liquid, before entrainment of the xenocrysts. The olivine cumulates were at magmatic temperatures (>1100??C) when the xenocrysts were entrained. Olivine at 1100??C has a rheology similar to ice, and the olivine cumulates should flow down and away from the summit of the volcano. Flow of the olivine cumulates places constant pressure on the unbuttressed seaward flank, leading to an extensional region that localizes deep intrusions behind the flank; these intrusions add to the seaward push. This mechanism ties the source of gravitational instability to the caldera complex and deep

  8. Iron isotopic systematics of oceanic basalts

    NASA Astrophysics Data System (ADS)

    Teng, Fang-Zhen; Dauphas, Nicolas; Huang, Shichun; Marty, Bernard

    2013-04-01

    The iron isotopic compositions of 93 well-characterized basalts from geochemically and geologically diverse mid-ocean ridge segments, oceanic islands and back arc basins were measured. Forty-three MORBs have homogeneous Fe isotopic composition, with δ56Fe ranging from +0.07‰ to +0.14‰ and an average of +0.105 ± 0.006‰ (2SD/√n, n = 43, MSWD = 1.9). Three back arc basin basalts have similar δ56Fe to MORBs. By contrast, OIBs are slightly heterogeneous with δ56Fe ranging from +0.05‰ to +0.14‰ in samples from Koolau and Loihi, Hawaii, and from +0.09‰ to +0.18‰ in samples from the Society Islands and Cook-Austral chain, French Polynesia. Overall, oceanic basalts are isotopically heavier than mantle peridotite and pyroxenite xenoliths, reflecting Fe isotope fractionation during partial melting of the mantle. Iron isotopic variations in OIBs mainly reflect Fe isotope fractionation during fractional crystallization of olivine and pyroxene, enhanced by source heterogeneity in Koolau samples.

  9. The fluid dynamics of a basaltic magma chamber replenished by influx of hot, dense ultrabasic magma

    NASA Astrophysics Data System (ADS)

    Huppert, Herbert E.; Sparks, R. Stephen J.

    1981-09-01

    This paper describes a fluid dynamical investigation of the influx of hot, dense ultrabasic magma into a reservoir containing lighter, fractionated basaltic magma. This situation is compared with that which develops when hot salty water is introduced under cold fresh water. Theoretical and empirical models for salt/water systems are adapted to develop a model for magmatic systems. A feature of the model is that the ultrabasic melt does not immediately mix with the basalt, but spreads out over the floor of the chamber, forming an independent layer. A non-turbulent interface forms between this layer and the overlying magma layer across which heat and mass are transferred by the process of molecular diffusion. Both layers convect vigorously as heat is transferred to the upper layer at a rate which greatly exceeds the heat lost to the surrounding country rock. The convection continues until the two layers have almost the same temperature. The compositions of the layers remain distinct due to the low diffusivity of mass compared to heat. The temperatures of the layers as functions of time and their cooling rate depend on their viscosities, their thermal properties, the density difference between the layers and their thicknesses. For a layer of ultrabasic melt (18% MgO) a few tens of metres thick at the base of a basaltic (10% MgO) magma chamber a few kilometres thick, the temperature of the layers will become nearly identical over a period of between a few months and a few years. During this time the turbulent convective velocities in the ultrabasic layer are far larger than the settling velocity of olivines which crystallise within the layer during cooling. Olivines only settle after the two layers have nearly reached thermal equilibrium. At this stage residual basaltic melt segregates as the olivines sediment in the lower layer. Depending on its density, the released basalt can either mix convectively with the overlying basalt layer, or can continue as a separate

  10. 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

  11. Olivine-Respiring Bacteria Isolated from the Rock-Ice Interface in a Lava-Tube Cave, a Mars Analog Environment

    PubMed Central

    Smith, Amy R.; Popa, Rodica; Boone, Jane; Fisk, Martin

    2012-01-01

    Abstract The boundary between ice and basalt on Earth is an analogue for some near-surface environments of Mars. We investigated neutrophilic iron-oxidizing microorganisms from the basalt-ice interface in a lava tube from the Oregon Cascades with perennial ice. One of the isolates (Pseudomonas sp. HerB) can use ferrous iron Fe(II) from the igneous mineral olivine as an electron donor and O2 as an electron acceptor. The optimum growth temperature is ∼12–14°C, but growth also occurs at 5°C. Bicarbonate is a facultative source of carbon. Growth of Pseudomonas sp. HerB as a chemolithotrophic iron oxidizer with olivine as the source of energy is favored in low O2 conditions (e.g., 1.6% O2). Most likely, microbial oxidation of olivine near pH 7 requires low O2 to offset the abiotic oxidation of iron. The metabolic capabilities of this bacterium would allow it to live in near-surface, icy, volcanic environments of Mars in the present or recent geological past and make this type of physiology a prime candidate in the search for life on Mars. Key Words: Extremophiles—Mars—Olivine—Iron-oxidizing bacteria—Redox. Astrobiology 12, 9–18. PMID:22165996

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

    NASA Astrophysics Data System (ADS)

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

    2002-06-01

    The concentrations and ratios of the major elements determine the physical properties and the phase equilibria behavior of peridotites and basalts in response to the changing energy contents of the systems. The behavior of the trace elements and isotopic features are influenced in their turn by the phase equilibria, by the physical character of the partial melting and partial crystallization processes, and by the way in which a magma interacts with its wall rocks. Concentrating on the trace element and isotope contents of basalts to the exclusion of the field relations, petrology, major element data, and phase equilibria is as improvident as slaughtering the buffalo for the sake of its tongue. The crust is a cool boundary layer and a density filter, which impedes the upward transfer of hot, dense "primary" picritic and komatiitic liquids. Planetary crusts are sites of large-scale contamination and extensive partial crystallization of primitive melts striving to escape to the surface. Escape of truly unmodified primitive melts to the surface is a rare event, requiring the resolution of daunting problems in chemical and mechanical engineering. Primary status for volumetrically abundant basalts such as mid-ocean ridge basalt, ocean island basalt, and continental flood basalts is denied by their low-pressure cotectic character, first remarked upon on petrological grounds in 1928 and on experimental grounds in 1962. These basalt liquids are products of crystal-liquid separation at low pressure. Primary status for these common basalts is further denied by the phase equilibria of such compositions at elevated pressures, when the required residual mantle mineralogy (magnesian olivine and orthopyroxene) is not stable at the liquidus. It is also denied by the picritic or komatiitic nature of partial melts of candidate upper-mantle compositions at high pressures - a conclusion supported by calculation of the melt composition, which would need to be extracted in order to

  13. Lu-Hf and Sm-Nd evolution in lunar mare basalts

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

    Unruh, D.M.; Stille, P.; Patchett, P.J.

    1984-02-15

    Lu-Hf and Sm-Nd data for mare basalts combined with Rb-Sr and total REE data taken from the literature suggest that the mare basalts were derived by small (< or =10%) degrees of partial melting of cumulate sources, but that the magma ocean from which these sources formed was light REE and Hf-enriched. Calculated source compositions range fromm lherzolite to olivine websterite. Nonmodal melting of small amounts of ilmenite (< or =3%) in the sources seems to be required by the Lu/Hf data. A comparison of the Hf and Nd isotopic characteristics between the mare basalts and terrestrial oceanic basalts revealsmore » that the epsilonHf/epsilonNd ratios of low-Ti mare basalts are much higher than in terrestrial oceanic basalts. The results are qualitatively consistent with the hypothesis that terrestrial basalt sources are partial melt residues whereas mare basalt sources are cumulates. Alternatively, the results may imply that the terrestrial mantle has evolved in two (or more) stages of evolution, and that the net effect was depletion of the mantle during the first approx.1-3 b.y. followed by enrichment during the last 1-2 b.y.; or simply that there is a difference in Lu-Hf crystal-liquid partitioning (relative to Sm-Nd) between the lunar and terrestrial mantles.« less

  14. Geochemistry of Central Snake River Plain Basalts From Camas Prairie to Glenns Ferry, Southern Idaho

    NASA Astrophysics Data System (ADS)

    Vetter, S. K.; Johnston, S. A.; Shervais, J.; Hanan, B.

    2006-12-01

    The Snake River Plain (SRP) of southern Idaho represents the track of a hot-spot (mantle plume) which links voluminous flood basalts of the Miocene Columbia River province to Quaternary volcanic centers at Island Park and Yellowstone. However, much of the volcanism associated with this province either lies off the main volcanic trend or differs in age from the postulated plume passage. The Camas Prairie and the Mount Bennett Hills lie north of the Snake River-Yellowstone plume track, near the intersection of the eastern and western Snake River Plain trends. Young basalt flows cap highlands overlooking the Snake River near King Hill, but farther north in the Mount Bennett Hills and Camas Prairie these young lava flows are juxtaposed against older basalts along a series of WNW trending normal faults. These older basalt flows rest directly on rhyolite of the Mount Bennett Hills, making them the oldest basalts known in outcrop in this area. The older basalts in the Mount Bennett Hills include at least six major flows with a total thickness of 110 m. Although they have been strongly dissected by erosion, they still cover an outcrop area of 300 km2 . Eighty samples were collected as part of our petrologic survey of basaltic volcanism in the central Snake River Plain. These samples were studied petrographically and analyzed for their major elements, trace elements, and REE. The basalts consist of plagioclase and olivine microphenocrysts set in a groundmass of olivine, plagioclase, clinopyroxene, oxides and interstitial glass. The majority of samples have Mg# ranging from 50- 59. However there are samples that are more evolved as indicated by Mg# ranging from less than 50 to 29. The high Mg# samples have the following chemical ranges: TiO2 0.87 - 2.6 wt.%; FeO 9.95 - 13.7 wt.%; Nb 8 to 23 ppm; Zr 111 to 243 ppm; Ni 81 to 151 ppm; La 10.9 to 26.9 ppm. The more evolved samples have TiO2 1.4 3.93 wt.%; FeO 9.7 16.8 wt%; Nb 11 to 40 ppm; Zr 110 to 500 ppm; Ni 4 to 85 ppm; La

  15. Vapor deposition in basaltic stalactites, Kilauea, Hawaii

    NASA Astrophysics Data System (ADS)

    Baird, A. K.; Mohrig, D. C.; Welday, E. E.

    Basaltic stalacties suspended from the ceiling of a large lava tube at Kilauea, Hawaii, have totally enclosed vesicles whose walls are covered with euhedral FeTi oxide and silicate crystals. The walls of the vesicles and the exterior surfaces of stalactites are Fe and Ti enriched and Si depleted compared to common basalt. Minerals in vesicles have surface ornamentations on crystal faces which include alkali-enriched, aluminosilicate glass(?) hemispheres. No sulfide-, chloride-, fluoride-, phosphate- or carbonate-bearing minerals are present. Minerals in the stalactites must have formed by deposition from an iron oxide-rich vapor phase produced by the partial melting and vaporization of wall rocks in the tube.

  16. Olivine tablets in peridotite xenoliths: Evidence for a static, foliation-producing recrystallization mechanism operative in the strained, fluid-bearing mantle

    NASA Astrophysics Data System (ADS)

    Špaček, Petr; Habler, Gerlinde; Krmíček, Lukáš; Libowitzky, Eugen

    2014-05-01

    The term "olivine tablet" is used for elongated, (sub-)idiomorphic, strain-free crystals of olivine with well developed parallel crystal faces, usually found in peridotite xenoliths. While only rarely occurring in basalt-hosted xenolith suites, such peculiar grains are relatively common in specific kimberlite-hosted peridotite xenoliths and often explained as a result of fluid-assisted recrystallization in xenoliths after their entrainment in host magma. Extremely well developed olivine tablets are common in some peridotite xenoliths from Pliocene Lutynia basanite (South Poland). These were studied in detail focusing on their crystallographic orientation and chemical composition in relation to their host grains, in order to learn more about their origin. The tablets are restricted to grain boundary regions of olivine(I) and enstatite or occur pervasively, in some cases constituting more than half of the rock volume. Together with strain-free mosaic grains they form a second generation of olivine growing at the expense of older and larger, strained olivine(I) grains. The tablets are typically 0.1-1 mm (up to 3 mm) long having typical aspect ratios of 2-3 (up to >10) and exhibit a strong shape preferred orientation at local scale or in the whole sample, in the latter case forming a distinct foliation in peridotite xenoliths. Tablet grains usually exhibit a lattice preferred orientation (LPOs) similar to the host olivine(I), suggesting that their orientation is inherited, likely by selective exaggerated growth of small grains at the margins of host grains (dynamically recrystallized grains were not observed directly). In some cases oriented growth of tablets along microcrackss, or planar sliding surfaces, is suggested by the microstructures. Traces of prominent tablet faces mostly correspond to (010) planes of tablet grains, while correlation to crystallographic orientations of host grains is poor. Compositional profiles across tablet/host grain boundaries (EMPA, long

  17. Elemental Abundance Distributions in Basalt Clays and Meteorites: Is It a Biosignature?

    NASA Technical Reports Server (NTRS)

    Fisk, M. R.; Storrie-Lombardi, M. C.; Joseph, J.

    2005-01-01

    Volcanic glass altered by microorganisms exhibits distinctive textures differing significantly from abiotic alteration [1-4]. We have previously presented morphological evidence of bioweathering in sub-oceanic basalt glass [5] and olivine [6], and noted similar alterations in Nakhla [7]. We have also introduced an autonomous Bayesian probabilistic classification methodology to identify biotic and abiotic alteration in sub-oceanic basalts using elemental abundance data [8]. We now present data from multiple sub-oceanic sites addressing the more general question of utilizing elemental abundance distribution in clays as a valid biosignature for the exploration of putative clay alteration products in meteorites.

  18. Shock and thermal metamorphism of basalt by nuclear explosion, Nevada test site

    USGS Publications Warehouse

    James, O.B.

    1969-01-01

    Olivine trachybasalt metamorphosed by nuclear explosion is classified into categories of progressive metamorphism: (i) Weak. Plagioclase is microfractured, and augite cotainis fine twin lamellae. (ii) Moderate. Plagioclase is converted to glass, and mafic minerals show intragranular deformation (undulatory extinction, twin lamellae, and, possibly, deformation lamellae), but rock texture is preserved. (iii) Moderately strong. Plagioclase glass shows small-scale flow, mafic minerals are fractured and show intragranular deformation, and rocks contain tension fractures. (iv) Strong. Plagioclase glass is vesicular, augite is minutely fractured, and olivine is coarsely fragmented, shows mosaic extinction, distinctive lamellar structures, and is locally recrystallized. (v) Intense. Rocks are converted to inhomogeneous basaltic glass.

  19. Water-in-Olivine Magma Ascent Chronometry: Every Crystal is a Clock

    NASA Astrophysics Data System (ADS)

    Newcombe, M. E.; Asimow, P. D.; Ferriss, E.; Barth, A.; Lloyd, A. S.; Hauri, E.; Plank, T. A.

    2017-12-01

    The syneruptive decompression rate of basaltic magma in volcanic conduits is thought to be a critical control on eruptive vigor. Recent efforts have constrained decompression rates using models of diffusive water loss from melt embayments (Lloyd et al. 2014; Ferguson et al. 2016), olivine-hosted melt inclusions (Chen et al. 2013; Le Voyer et al. 2014), and clinopyroxene phenocrysts (Lloyd et al. 2016). However, these techniques are difficult to apply because of the rarity of melt embayments and clinopyroxene phenocrysts suitable for analysis and the complexities associated with modeling water loss from melt inclusions. We are developing a new magma ascent chronometer based on syneruptive diffusive water loss from olivine phenocrysts. We have found water zonation in every olivine phenocryst we have measured, from explosive eruptions of Pavlof, Seguam, Fuego, Cerro Negro and Kilauea volcanoes. Phenocrysts were polished to expose a central plane normal to the crystallographic `b' axis and volatile concentration profiles were measured along `a' and `c' axes by SIMS or nanoSIMS. Profiles are compared to 1D and 3D finite-element models of diffusive water loss from olivine, with or without melt inclusions, whose boundaries are in equilibrium with a melt undergoing closed-system degassing. In every case, we observe faster water diffusion along the `a' axis, consistent with the diffusion anisotropy observed by Kohlstedt and Mackwell (1998) for the so-called `proton-polaron' mechanism of H-transport. Water concentration gradients along `a' match the 1D diffusion model with a diffusivity of 10-10 m2/s (see Plank et al., this meeting), olivine-melt partition coefficient of 0.0007­-0.002 (based on melt inclusion-olivine pairs), and decompression rates equal to the best-fit values from melt embayment studies (Lloyd et al. 2014; Ferguson et al. 2016). Agreement between the melt embayment and water-in-olivine ascent chronometers at Fuego, Seguam, and Kilauea Iki demonstrates the

  20. NanoSIMS results from olivine-hosted melt embayments: Modeling ascent rate in explosive basaltic eruptions

    NASA Astrophysics Data System (ADS)

    Lloyd, A. S.; Plank, T.; Ruprecht, P.; Hauri, E. H.; Gonnermann, H. M.; Rose, W. I.

    2012-12-01

    A critical parameter governing the explosivity of volcanic eruptions is the rate at which magma ascends and degases, because this affects bubble nucleation, coalescence, and ultimately fragmentation. Although several methods have been used to determine magma ascent rates, it remains a poorly constrained parameter for most eruptions. One promising method employs diffusion modeling of H2O and CO2 concentration gradients in melt embayments/open melt inclusions [1,2]. Here we utilize the fine spatial resolution of the nanoSIMS to obtain concentration gradients for five volatile species, improving upon previous efforts that were more limited in spatial resolution (FTIR, [1]) and in number of volatile analytes (H2O only by BSE, [2]). Focusing on explosive basaltic eruptions, for which very little is known about ascent rates, we chose ash and lapilli samples from the Oct 1974 sub-plinian eruption of Volcán de Fuego. Glassy, olivine-hosted embayments with evidence of outlet bubbles were analyzed by nanoSIMS at a minimum distance between spots of 15 μm. Major element zonation in the embayments was investigated by EMP, and high resolution BSE images were captured to complement the nanoSIMS spot measurements for H2O (as in [2]). We report analyses for 5 embayments that vary in length from 100 to 350 μm. Low-solubility volatiles (CO2, H2O, S) decrease towards the embayment outlet, consistent with diffusive reequilibration with the more-degassed surrounding melt. High-solubility volatiles (Cl, F) increase towards the outlet, apparently behaving as magmaphile elements. Major elements exhibit constant concentrations along the embayment, except for a 20-50 μm wide zone near the embayment outlet, perhaps representing a boundary layer at the outlet bubble, where concentrations vary consistent with olivine and clinopyroxene microlite growth. BSE grayscale values are thus affected by both H2O diffusion and major element zonation at the embayment outlet, and cannot be used to

  1. Chromium valences in ureilite olivine and implications for ureilite petrogenesis

    NASA Astrophysics Data System (ADS)

    Goodrich, C. A.; Sutton, S. R.; Wirick, S.; Jercinovic, M. J.

    2013-12-01

    basaltic melt composition), consistent with fO2 values obtained by assuming olivine-silica-iron metal (OSI) equilibrium. For the primary chromite-bearing-ureilites, the corresponding fO2 were estimated (again, assuming basaltic melt composition) to be ∼IW to IW+1.0, i.e., several orders of magnitude more oxidizing than the conditions estimated for the chromite-free ureilites. In terms of Fo and Cr valence properties, ureilites appear to form two groups rather than a single “Cr-valence (or fO2) vs. Fo” trend. The chromite-bearing ureilites show little variation in Fo (∼74-76) but significant variation in Cr valence, while the non-chromite-bearing ureilites show significant variation in Fo (∼77-95) and little variation in Cr valence. These groups are unrelated to petrologic type (i.e., olivine-pigeonite, olivine-orthopyroxene, or augite-bearing). The chromite-bearing ureilites also have lower contents of Cr in olivine than most non-chromite-bearing ureilites, consistent with predictions based on Cr olivine/melt partitioning in spinel saturated vs. non-spinel-saturated systems. Under the assumption that at magmatic temperatures graphite-gas equilibria controlled fO2 at all depths on the ureilite parent body, we conclude: (1) that ureilite precursor materials having the Fo and Cr valence properties now observed in ureilites are unlikely to have been preserved during planetary processing; and (2) that the Fo and Cr valence properties now observed in ureilites are consistent with having been established by high-temperature carbon redox control over a range of depths on a plausible-sized ureilite parent body. The apparent limit on ureilite Fo values around 74-76 suggests that the precursor material(s) had bulk mg# ⩾ that of LL chondrites.

  2. Effect of Fluorine on Near-Liquidus Phase Equilibria of Basalts

    NASA Technical Reports Server (NTRS)

    Filiberto, Justin; Wood, Justin; Loan, Le; Dasgupta, Rajdeep; Shimizu, Nobumichi; Treiman, Allan H.

    2010-01-01

    Volatile species such as H2O, CO2, F, and Cl have significant impact in generation and differentiation of basaltic melts. Thus far experimental work has primarily focused on the effect of water and carbon dioxide on basalt crystallization, liquid-line of descent, and mantle melting [e.g., 1, 2] and the effects of halogens have received far less attention [3-4]. However, melts in the planetary interiors can have non-negligible chlorine and fluorine concentrations. Here, we explore the effects of fluorine on near-liquidus phase equilibria of basalt. We have conducted nominally anhydrous piston cylinder experiments using graphite capsules at 0.6 - 1.5 GPa on an Fe-rich model basalt composition. 1.75 wt% fluorine was added to the starting mix in the form of AgF2. Fluorine in the experimental glass was measured by SIMS and major elements of glass and minerals were analyzed by EPMA. Nominally volatile free experiments yield a liquidus temperature from 1330 C at 0.8GPa to 1400 at 1.6GPa and an olivine(Fo72)-pyroxene(En68)-liquid multiple saturation point at 1.25 GPa and 1375 C. The F-bearing experiments yield a liquiudus temperature from 1260 C at 0.6GPa to 1305 at 1.5GPa and an ol(Fo66)-pyx(En64)-MSP at 1 GPa and 1260 C. This shows that F depresses the basalt liquidus, extends the pyroxene stability field to lower pressure, and forces the liquidus phases to be more Fe-rich. KD(Fe-Mg/mineral-melt) calculated for both pyroxenes and olivines show an increase with increasing F content of the melt. Therefore, we infer that F complexes with Mg in the melt and thus increases the melt s silica activity, depressing the liquidus and changing the composition of the crystallizing minerals. Our study demonstrates that on a weight percent basis, the effect of fluorine is similar to the effect of H2O [1] and Cl [3] on freezing point depression of basalts. But on an atomic fraction basis, the effect of F on liquidus depression of basalts is xxxx compared to the effect of H. Future

  3. Valence of Ti, V, and Cr in Apollo 14 aluminous basalts 14053 and 14072

    NASA Astrophysics Data System (ADS)

    Simon, Steven B.; Sutton, Stephen R.

    2017-09-01

    The valences of Ti, V, and Cr in olivine and pyroxene, important indicators of the fO2 of the source region of their host rocks, can be readily measured nondestructively by XANES (X-ray absorption near edge structure) spectroscopy, but little such work has been done on lunar rocks, and there is some uncertainty regarding the presence of Ti3+ in lunar silicates and the redox state of the lunar mantle. This is the first study involving direct XANES measurement of valences of multivalent cations in lunar rocks. Because high alumina activity facilitates substitution of Ti cations into octahedral rather than tetrahedral sites in pyroxene and Ti3+ only enters octahedral sites, two aluminous basalts from Apollo 14, 14053 and 14072, were studied. Most pyroxene contains little or no detectable Ti3+, but in both samples relatively early, magnesian pyroxene was found that has Ti valences that are not within error of 4; in 14053, this component has an average Ti valence of 3.81 ± 0.06 (i.e., Ti3+/[Ti3+ + Ti4+ = 0.19]). This pyroxene has relatively low atomic Ti/Al ratios (<0.4) due to crystallization before plagioclase, contrary to the long-held belief that lunar pyroxene with Ti/Al > 0.5 contains Ti3+ and pyroxene with lower ratios does not. Later pyroxene, with lower Mg/Fe and higher Ti/Al ratios, has higher proportions of Ti (all Ti4+) in tetrahedral sites. All pyroxene analyzed contains divalent Cr, ranging from 15 to 30% of the Cr present, and all but one analysis spot contains divalent V, accounting for 0 to 40% (typically 20-30%) of the V present. Three analyses of olivine in 14053 do not show any Ti3+, but Ti valences in 14072 olivine range from 4 down to 3.70 ± 0.10. In 14053 olivine, 50% of the Cr and 60% of the V are divalent. In 14072 olivine, the divalent percentages are 20% for Cr and 20-60% for V. These results indicate significant proportions of divalent Cr and V and limited amounts of trivalent Ti in the parental melts, especially when crystal

  4. Review on effect of chemical, thermal, additive treatment on mechanical properties of basalt fiber and their composites

    NASA Astrophysics Data System (ADS)

    Jain, Naman; Singh, Vinay Kumar; Chauhan, Sakshi

    2017-12-01

    Basalt fiber is emerging out the new reinforcing material for composites. To overcome some of the disadvantages of fibers such as poor bonding to polymers, low thermal stability and high moisture absorption fiber characteristics are modified with chemical, thermal and additive treatments. Chemical treatment corrosive resistance to alkali and acid were investigated which were used to clean and modify the surface of fiber for higher bonding with resins. To improve the thermal stability and reduce moisture uptake thermal treatment such as plasma and non thermal plasma were used which increased the surface roughness and change the chemical composition of surface of basalt fiber. Additive treatment is used to improve the mechanical properties of fibers, in basalt fiber additive treatment was done with SiO2 additive because of its chemical composition which contains major content of SiO2. In present investigation review on the effect of different treatment such as chemical, thermal and additive were studied. Effect of these treatment on chemical composition of the surface of basalt fiber and corrosion to acidic and alkali solution were studied with their effect on mechanical properties of basalt fiber and their composite.

  5. Magma Differentiation and Storage Inferred from Crystal Textures at Harrat Rahat Volcanic Field, Kingdom of Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Witter, M. R.; Mahood, G. A.; Stelten, M. E.; Downs, D. T.; Zahran, H. M.

    2015-12-01

    We present results of a petrographic study of Harrat Rahat volcanic field in western Saudi Arabia as part of a collaborative project between the U.S.G.S. and the Saudi Geological Survey. Lavas range in composition from alkali basalt to trachyphonolite. Basalts have <2-10 vol.% phenocrysts of euhedral olivine and plagioclase (± minor clinopyroxene). In intermediate lavas, phenocrysts (<5 vol.%) of olivine and plagioclase are resorbed, and plagioclase also exhibits sieve textures and strong zoning, indicative of complex magmatic histories. Trachyphonolite lavas have 0-35 vol.% large phenocrysts of anorthoclase and trace fayalitic olivine but are characterized by a size distribution of crystals that is seriate in hand specimen, so that most exceeded 45% crystals at the time of eruption. Some contain groundmass alkali amphibole. Crystal size distributions (CSD) of crystal-rich trachyphonolites produce simple linear trends (see below), which are interpreted as signifying that all the crystals are related through a common nucleation and growth history, at more or less constant pressure. Linear CSDs indicate no loss of small crystals due to reheating of magmas by recharge, no gain of small crystals due to late-stage nucleation on ascent or degassing, and no addition of large phenocrysts by crystal accumulation or magma mixing. Experimental studies demonstrate that silica-undersaturated evolved magmas like those erupted at Harrat Rahat can form by fractionation of alkali basalts at crustal depths greater than ~25 km. The observed phenocryst assemblage in the trachyphonolites, however, forms at shallow depths, ~2-4 km, according to MELTS modeling. Coupled with CSD data, this suggests that deep extraction events yield crystal-poor trachyphonolite magmas that rise to the upper crust where they undergo crystallization. Extensive shallow crystallization of trachyphonolites may have triggered eruptions by causing vapor saturation, which lowers magma density via vesiculation and

  6. A Tale of Two Olivines: Magma Ascent in the Auckland Volcanic Field, New Zealand

    NASA Astrophysics Data System (ADS)

    Smid, E. R.; McGee, L. E.; Smith, I. E.; Lindsay, J. M.

    2013-12-01

    The Auckland Volcanic Field (AVF) is a nephelinitic to subalkali basaltic monogenetic field centered on the city of Auckland, New Zealand. Lavas are olivine-phyric, and the deposits of several volcanoes in the field contain olivine crystals with chrome spinel (Cr-spinel) inclusions. Microprobe analyses show at least two populations of olivine, categorised by their Mg# and their spinel inclusion compositions: the first has olivines that are euhedral, have compositions slightly less forsteritic than expected for whole rock Mg#, and have Cr-spinel inclusions with relatively low Cr2O3 contents of ~20%. These are interpreted as antecrysts inherited from the mantle source that yielded their host magma. The second population is characterised by olivines that are sub- to euhedral, are significantly more forsteritic than expected from their host whole rock Mg#, and have Cr-spinel inclusons with relatively high Cr2O3 contents of ~50%. These are interpreted as xenocrysts. The composition of these high Cr2O3 spinels very closely resembles the composition of spinels within olivines in dunite sampled from the Dun Mountain Ophiolite on the South Island of New Zealand. The northward extension of the Dun Mountain complex beneath the North Island is defined by the Junction Magnetic Anomaly, marking a crustal terrane boundary that underlies the Auckland Volcanic Field. These data indicate that the magmas that have risen to produce the volcanoes of the Auckland Volcanic Field have carried crystals from an underlying ultramafic crust as well as from their asthenospheric source. Euhedral olivine crystals which do not contain Cr-spinel are also present in AVF lavas and these are interpreted as true phenocrysts that crystallised directly from their host magmas. The lack of reaction textures at crystal margins suggests rapid ascent rates. A crustal origin for the xenocrysts not only has large implications for ascent rate modelling of olivines, but also for the crustal structure of the

  7. Bulk rock composition and geochemistry of olivine-hosted melt inclusions in the Grey Porri Tuff and selected lavas of the Monte dei Porri volcano, Salina, Aeolian Islands, southern Italy

    USGS Publications Warehouse

    Doherty, Angela L.; Bodnar, Robert J.; De Vivo, Benedetto; Bohrson, Wendy A.; Belkin, Harvey E.; Messina, Antonia; Tracy, Robert J.

    2012-01-01

    The Aeolian Islands are an arcuate chain of submarine seamounts and volcanic islands, lying just north of Sicily in southern Italy. The second largest of the islands, Salina, exhibits a wide range of compositional variation in its erupted products, from basaltic lavas to rhyolitic pumice. The Monte dei Porri eruptions occurred between 60 ka and 30 ka, following a period of approximately 60,000 years of repose. The bulk rock composition of the Monte dei Porri products range from basaltic-andesite scoria to andesitic pumice in the Grey Porri Tuff (GPT), with the Monte dei Porri lavas having basaltic-andesite compositions. The typical mineral assemblage of the GPT is calcic plagioclase, clinopyroxene (augite), olivine (Fo72−84) and orthopyroxene (enstatite) ± amphibole and Ti-Fe oxides. The lava units show a similar mineral assemblage, but contain lower Fo olivines (Fo57−78). The lava units also contain numerous glomerocrysts, including an unusual variety that contains quartz, K-feldspar and mica. Melt inclusions (MI) are ubiquitous in all mineral phases from all units of the Monte dei Porri eruptions; however, only data from olivine-hosted MI in the GPT are reported here. Compositions of MI in the GPT are typically basaltic (average SiO2 of 49.8 wt %) in the pumices and basaltic-andesite (average SiO2 of 55.6 wt %) in the scoriae and show a bimodal distribution in most compositional discrimination plots. The compositions of most of the MI in the scoriae overlap with bulk rock compositions of the lavas. Petrological and geochemical evidence suggest that mixing of one or more magmas and/or crustal assimilation played a role in the evolution of the Monte dei Porri magmatic system, especially the GPT. Analyses of the more evolved mineral phases are required to better constrain the evolution of the magma.

  8. 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

  9. 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

  10. Melt rock components in KREEPy breccia 15205: Petrography and mineral chemistry of KREEP basalts and quartz-normative mare basalts

    NASA Astrophysics Data System (ADS)

    Shervais, John W.; Vetter, Scott K.

    1993-05-01

    Many current models for the origin of lunar highland rocks feature as an essential component the assimilation of KREEPy material by primitive magmas parental to the Mg-rich suite and alkali suite plutonic rocks. Similar models have also been proposed for the origin of various mare basalt suites. However, any model which considers assimilation of KREEP an important petrologic process must sooner-or-later deal with the question: what is KREEP? Because pristine KREEP basalts are rare, and most known samples are small (e.g., 15382/15386), the geochemical variability of KREEP basalts is poorly known. Other KREEP compositions which are commonly used in these models include the hypothetical 'high-K KREEP' component of Warren and Wasson, which is derived from Apollo 14 soil data, and the 'superKREEP' quartz-monzodiorite 15405. Lunar breccia 15205 is a polymict regolith breccia that consists of approximately 20% KREEP basalt clasts and 20% quartz-normative basalt clasts in a KREEP-rich matrix. Bulk rock mixing calculations show that this sample comprises about 84% KREEP. The clasts range up to 1 cm in size, but most are considerably smaller. The primary aim is to characterize pristine KREEP basalts petrographically, to establish the range in chemical compositions of KREEP basalts, and to test models that were proposed for their origin. In addition, we may be able to extend the compositional range recognized in the quartz-normative basalt suite and cast some light on its origin as well. Preliminary whole rock geochemical data on the KREEP basalts are presented in a companion paper by M.M. Lindstrom and co-workers. Concentration is on petrography and mineral chemistry of these clasts, and the implications these data have for the origin of the different melt rock suites.

  11. Melt rock components in KREEPy breccia 15205: Petrography and mineral chemistry of KREEP basalts and quartz-normative mare basalts

    NASA Technical Reports Server (NTRS)

    Shervais, John W.; Vetter, Scott K.

    1993-01-01

    Many current models for the origin of lunar highland rocks feature as an essential component the assimilation of KREEPy material by primitive magmas parental to the Mg-rich suite and alkali suite plutonic rocks. Similar models have also been proposed for the origin of various mare basalt suites. However, any model which considers assimilation of KREEP an important petrologic process must sooner-or-later deal with the question: what is KREEP? Because pristine KREEP basalts are rare, and most known samples are small (e.g., 15382/15386), the geochemical variability of KREEP basalts is poorly known. Other KREEP compositions which are commonly used in these models include the hypothetical 'high-K KREEP' component of Warren and Wasson, which is derived from Apollo 14 soil data, and the 'superKREEP' quartz-monzodiorite 15405. Lunar breccia 15205 is a polymict regolith breccia that consists of approximately 20% KREEP basalt clasts and 20% quartz-normative basalt clasts in a KREEP-rich matrix. Bulk rock mixing calculations show that this sample comprises about 84% KREEP. The clasts range up to 1 cm in size, but most are considerably smaller. The primary aim is to characterize pristine KREEP basalts petrographically, to establish the range in chemical compositions of KREEP basalts, and to test models that were proposed for their origin. In addition, we may be able to extend the compositional range recognized in the quartz-normative basalt suite and cast some light on its origin as well. Preliminary whole rock geochemical data on the KREEP basalts are presented in a companion paper by M.M. Lindstrom and co-workers. Concentration is on petrography and mineral chemistry of these clasts, and the implications these data have for the origin of the different melt rock suites.

  12. Crust recycling induced compositional-temporal-spatial variations of Cenozoic basalts in the Trans-North China Orogen

    NASA Astrophysics Data System (ADS)

    Xu, Rong; Liu, Yongsheng; Wang, Xiaohong; Zong, Keqing; Hu, Zhaochu; Chen, Haihong; Zhou, Lian

    2017-03-01

    It has been advocated that the stagnant Pacific slab within the mantle transition zone played a critical role in the genesis of the Cenozoic basalts in the eastern part of the North China Craton (NCC); however, it is not clear whether this recycled oceanic crust contributed to the chemical makeup of the Cenozoic basalts in the Trans-North China Orogen (TNCO, the central zone of the NCC). Here, we show that Cenozoic basalts from the TNCO are featured by low CaO contents, high TiO2 and FeOT contents and high Fe/Mn and Zn/Fe ratios, indicating a mantle source of pyroxenite. Temporally, these basalts evolved from alkali basalts of Late Eocene-Oligocene age to coexisting alkali and tholeiitic basalts of Late Miocene-Quaternary age. Spatially, their isotopic and chemical compositions vary symmetrically from the center to both the north and the south sides along the TNCO, i.e., SiO2 contents and 87Sr/86Sr ratios increase, FeOT contents and 143Nd/144Nd, Sm/Yb and Ce/Pb ratios decrease. The estimated average melting pressure of the TNCO tholeiitic basalts ( 3 GPa) agrees well with the present lithosphere thickness beneath the north region of the TNCO ( 90-120 km). The temporal and spatial chemical variations of Cenozoic basalts in the TNCO suggest that the recycled oceanic crust in the mantle of the TNCO is mainly related to the southward subduction of the Paleo-Asian oceanic plate and the northward subduction of the Tethyan ocean plate. The westward subduction of Pacific slab may not have contributed much than previously thought.

  13. Models of corundum origin from alkali basaltic terrains: a reappraisal

    NASA Astrophysics Data System (ADS)

    Lin Sutherland, F.; Hoskin, Paul W. O.; Fanning, C. Mark; Coenraads, Robert R.

    Corundums from basalt fields, particularly in Australia and Asia, include a dominant blue-green-yellow zoned ``magmatic'' suite (BGY suite) and subsidiary vari-coloured ``metamorphic'' suites. The BGY corundums have distinctive trace element contents (up to 0.04 wt% Ga2O3 and low Cr/Ga and Ti/Ga ratios <1). Different melt origins for BGY corundums are considered here from their inclusion and intergrowth mineralogy, petrologic associations and tectonic setting. Analysed primary inclusion minerals (over 100 inclusions) cover typical feldspars, zircon and Nb-Ta oxides and also include hercynite-magnetite, gahnospinel, rutile-ilmenite solid solution, calcic plagioclase, Ni-rich pyrrhotite, thorite and low-Si and Fe-rich glassy inclusions. This widens a previous inclusion survey; New England, East Australia corundums contain the most diverse inclusion suite known from basalt fields (20 phases). Zircon inclusion, intergrowth and megacryst rare earth element data show similar patterns, except for Eu which shows variable depletion. Temperature estimates from magnetite exsolution, feldspar compositions and fluid inclusion homogenization suggest that some corundums crystallized between 685-900°C. Overlap of inclusion Nb, Ta oxide compositions with new comparative data from niobium-yttrium-fluorine enriched granitic pegmatites favour a silicate melt origin for the corundums. The feasibility of crystallizing corundum from low-volume initial melting of amphibole-bearing mantle assemblages was tested using the MELTS program on amphibole-pyroxenite xenolith chemistry from basalts. Corundum appears in the calculations at 720-880°C and 0.7-1.1GPa with residual feldspathic assemblages that match mineral compositions found in corundums and their related xenoliths. A model that generates melts from amphibole-bearing lithospheric mantle during magmatic plume activity is proposed for BGY corundum formation.

  14. Rb-Sr Isotopic Systematics of Alkali-Rich Fragments in the Yamato-74442 LL-Chondritic Breccia

    NASA Technical Reports Server (NTRS)

    Yokoyama, T.; Misawa, K.; Okano, O.; Shih, C.-Y.; Nyquist, L. E.; Simo, J. I.; Tappa, M. J.; Yoneda, S.

    2012-01-01

    Alkali-rich igneous fragments were identified in the brecciated LL-chondrites, Kr henberg (LL5)], Bhola (LL3-6) and Yamato (Y)-74442 (LL4), and show characteristic fractionation patterns of alkaline elements. The K-Rb-Cs-rich fragments in Kr henberg, Bhola, and Y-74442 are very similar in mineralogy and petrography (olivine + pyroxene + glass), suggesting that they could have come from related precursor materials. We have undertaken Rb-Sr isotopic studies on alkali-rich fragments in Y-74442 to precisely determine their crystallization ages and the isotopic signatures of their precursor material(s).

  15. Melt density and the average composition of basalt

    NASA Technical Reports Server (NTRS)

    Stolper, E.; Walker, D.

    1980-01-01

    Densities of residual liquids produced by low pressure fractionation of olivine-rich melts pass through a minimum when pyroxene and plagioclase joint the crystallization sequence. The observation that erupted basalt compositions cluster around the degree of fractionation from picritic liquids corresponding to the density minimum in the liquid line of descent may thus suggest that the earth's crust imposes a density fiber on the liquids that pass through it, favoring the eruption of the light liquids at the density minimum over the eruption of denser more fractionated and less fractionated liquids.

  16. Automated identification of basalt spectra in Clementine lunar data

    NASA Astrophysics Data System (ADS)

    Antonenko, I.; Osinski, G. R.

    2011-06-01

    The identification of fresh basalt spectra plays an important role in lunar stratigraphic studies; however, the process can be time consuming and labor intensive. Thus motivated, we developed an empirically derived algorithm for the automated identification of fresh basalt spectra from Clememtine UVVIS data. This algorithm has the following four parameters and limits: BC Ratio=3(R950-R900)/(R900-R750)<1.1, CD Delta=(R1000-R950)/R750-1.09(R950-R900)/R750>0.003 and <0.06, B Slope=(R900-R750)/(3R750)<-0.012, and Band Depth=(R750-R950)/(R750-R415)>0.1, where R750 represents the unnormalized reflectance of the 750 nm Clementine band, and so on. Algorithm results were found to be accurate to within an error of 4.5% with respect to visual classification, though olivine spectra may be under-represented. Overall, fresh basalts identified by the algorithm are consistent with expectations and previous work in the Mare Humorum area, though accuracy in other areas has not yet been tested. Great potential exists in using this algorithm for identifying craters that have excavated basalts, estimating the thickness of mare and cryptomare deposits, and other applications.

  17. Occurrence and Mineral Chemistry of High Pressure Phases, Potrillo Basalt, Southcentral New Mexico. M.S. Thesis Final Technical Report, 1 Jun. 1980 - 31 May 1982

    NASA Technical Reports Server (NTRS)

    Sheffield, T. M.

    1982-01-01

    The presence of an older plagioclase-rich basalt and a younger olivine-rich basalt were confirmed by modal and chemical analysis. Chemical analysis also confirmed the presence of flows that are tholeiitic in composition and could be remnants of an original tholeittic parent magma. Eruptions from different levels of a differentiated magma chamber are proposed to account for the two members.

  18. Artificial meteor ablation studies: Olivine

    NASA Technical Reports Server (NTRS)

    Blanchard, M. B.; Cunningham, G. G.

    1973-01-01

    Artificial meteor ablation was performed on a Mg-rich olivine sample using an arc-heated plasma of ionized air. Experimental conditions simulated a meteor traveling about 12 km/sec at an altitude of 70 km. The mineral content of the original olivine sample was 98% olivine (including traces of olivine alteration products) and 2% chromite. Forsterite content of the original olivine was Fo-89. After ablation, the forsterite content had increased to Fo-94 in the recrystallized olivine. In addition, lamella-like intergrowths of magnetite were prevalent constituents. Wherever magnetite occurred, there was an increase in Mg and a corresponding decrease in Fe for the recrystallized olivine. The Allende fusion crust consisted of a recrystallized olivine, which was more Mg-rich and Fe-deficient than the original meteorite's olivine, and abundant magnetite grains. Although troilite and pentlandite were the common opaque mineral constituents in this meteorite, magnetite was the principal opaque mineral found in the fusion crust.

  19. Origin of major element chemical trends in DSDP Leg 37 basalts, Mid-Atlantic Ridge

    USGS Publications Warehouse

    Byerly, G.R.; Wright, T.L.

    1978-01-01

    In this paper we summarize the major element chemical variation for basalts from the Deep Sea Drilling Project Leg 37 and relate it to stratigraphic position in each of five drilling sites. Least-squares techniques are successfully used to quantify the nature and extent of alteration in these basalts, and to correct the major element analysis back to a magmatic, or alteration-free, composition on the assumption that alteration takes place in two ways: (1) secondary minerals are introduced into veins and vesicles, and (2) CO2 and H2O react with components in the rock to form a simple alteration assemblage. A chemical stratigraphy is defined for these basalts by grouping lavas whose chemistries are related by low-pressure phenocryst-liquid differentiation as identified by least-squares calculation. Major chemical-stratigraphic units are as much as 200 m thick; correlations of these units can be made between the holes at site 332 (about 100 m apart), but not between the other sites. Compositions of parental magmas are calculated by extrapolating low-pressure variations to a constant value of 9% MgO. The differences in these extrapolated compositions reflect high-pressure processes, and suggest that clinopyroxene may be an important phase in either intermediate-level fractionation of basaltic liquids, or as a residual phase during the partial melting which produces these basaltic liquids. Several of the basaltic liquids calculated as parental to the Leg 37 basalts have CaO contents greater than 14% and indicate that the oceanic mantle is richer in CaO and Al2O3 than values used in pyrolite models for the upper mantle. A model for magma generation and eruption beneath the Mid-Atlantic Ridge embodies the following characteristics: 1. (1) Separate magma batches are generated in the mantle. 2. (2) Each of these may be erupted directly or stored at shallow depth where significant fractionation takes place. Common fractionation processes are inferred to be gravitative

  20. Surface exposure dating of Holocene basalt flows and cinder cones in the Kula volcanic field (western Turkey) using cosmogenic 3He and 10Be

    NASA Astrophysics Data System (ADS)

    Heineke, Caroline; Niedermann, Samuel; Hetzel, Ralf; Akal, Cüneyt

    2015-04-01

    The Kula volcanic field is the youngest volcanic province in western Anatolia and covers an area of about 600 km2 around the town Kula (Richardson-Bunbury, 1996). Its alkali basalts formed by melting of an isotopically depleted mantle in a region of long-lived continental extension and asthenospheric upwelling (Prelevic et al., 2012). Based on morphological criteria and 40Ar/39Ar dating, four phases of Quaternary activity have been distinguished in the Kula volcanic field (Richardson-Bunbury, 1996; Westaway et al., 2006). The youngest lava flows are thought to be Holocene in age, but so far only one sample from this group was dated by 40Ar/39Ar at 7±2 ka (Westaway et al., 2006). In this study, we analysed cosmogenic 3He in olivine phenocrysts from three basalt flows and one cinder cone to resolve the Holocene history of volcanic eruptions in more detail. In addition, we applied 10Be exposure dating to two quartz-bearing xenoliths found at the surface of one flow and at the top of one cinder cone. The exposure ages fall in the range between ~500 and ~3000 years, demonstrating that the youngest volcanic activity is Late Holocene in age and therefore distinctly younger than previously envisaged. Our results show that the Late Holocene lava flows are not coeval but formed over a period of a few thousand years. We conclude that surface exposure dating of very young volcanic rocks provides a powerful alternative to 40Ar/39Ar dating. References Prelevic, D., Akal, C. Foley, S.F., Romer, R.L., Stracke, A. and van den Bogaard, P. (2012). Ultrapotassic mafic rocks as geochemical proxies for post-collisional dynamics of orogenic lithospheric mantle: the case of southwestern Anatolia, Turkey. Journal of Petrology, 53, 1019-1055. Richardson-Bunbury, J.M. (1996). The Kula Volcanic Field, western Turkey: the development of a Holocene alkali basalt province and the adjacent normal-faulting graben. Geological Magazine, 133, 275-283. Westaway, R., Guillou, H., Yurtmen, S., Beck, A

  1. Investigation of magnesium isotope fractionation during basalt differentiation: Implications for a chondritic composition of the terrestrial mantle

    USGS Publications Warehouse

    Teng, F.-Z.; Wadhwa, M.; Helz, R.T.

    2007-01-01

    To investigate whether magnesium isotopes are fractionated during basalt differentiation, we have performed high-precision Mg isotopic analyses by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) on a set of well-characterized samples from Kilauea Iki lava lake, Hawaii, USA. Samples from the Kilauea Iki lava lake, produced by closed-system crystal-melt fractionation, range from olivine-rich cumulates to highly differentiated basalts with MgO content ranging from 2.37 to 26.87??wt.%. Our results demonstrate that although these basalts have diverse chemical compositions, mineralogies, crystallization temperatures and degrees of differentiation, their Mg isotopic compositions display no measurable variation within the limits of our external precision (average ??26Mg = - 0.36 ?? 0.10 and ??25Mg = - 0.20 ?? 0.07; uncertainties are 2SD). This indicates that Mg isotopic fractionation during crystal-melt fractionation at temperatures of ??? 1055????C is undetectable at the level of precision of the current investigation. Calculations based on our data suggest that at near-magmatic temperatures the maximum fractionation in the 26Mg/24Mg ratio between olivine and melt is 0.07???. Two additional oceanic basalts, two continental basalts (BCR-1 and BCR-2), and two primitive carbonaceous chondrites (Allende and Murchison) analyzed in this study have Mg isotopic compositions similar to the Kilauea Iki lava lake samples. In contrast to a recent report [U. Wiechert, A.N. Halliday, Non-chondritic magnesium and the origins of the inner terrestrial planets, Earth and Planetary Science Letters 256 (2007) 360-371], the results presented here suggest that the Bulk Silicate Earth has a chondritic Mg isotopic composition. ?? 2007.

  2. Viscous flow behavior of tholeiitic and alkaline Fe-rich martian basalts

    NASA Astrophysics Data System (ADS)

    Chevrel, Magdalena Oryaëlle; Baratoux, David; Hess, Kai-Uwe; Dingwell, Donald B.

    2014-01-01

    The chemical compositions of martian basalts are enriched in iron with respect to terrestrial basalts. Their rheology is poorly known and liquids of this chemical composition have not been experimentally investigated. Here, we determine the viscosity of five synthetic silicate liquids having compositions representative of the diversity of martian volcanic rocks including primary martian mantle melts and alkali basalts. The concentric cylinder method has been employed between 1500 °C and the respective liquidus temperatures of these liquids. The viscosity near the glass transition has been derived from calorimetric measurements of the glass transition. Although some glass heterogeneity limits the accuracy of the data near the glass transition, it was nevertheless possible to determine the parameters of the non-Arrhenian temperature-dependence of viscosity over a wide temperature range (1500 °C to the glass transition temperature). At superliquidus conditions, the martian basalt viscosities are as low as those of the Fe-Ti-rich lunar basalts, similar to the lowest viscosities recorded for terrestrial ferrobasalts, and 0.5 to 1 order of magnitude lower than terrestrial tholeiitic basalts. Comparison with empirical models reveals that Giordano et al. (2008) offers the best approximation, whereas the model proposed by Hui and Zhang (2007) is inappropriate for the compositions considered. The slightly lower viscosities exhibited by the melts produced by low degree of mantle partial melting versus melts produced at high degree of mantle partial melting (likely corresponding to the early history of Mars), is not deemed sufficient to lead to viscosity variations large enough to produce an overall shift of martian lava flow morphologies over time. Rather, the details of the crystallization sequence (and in particular the ability of some of these magmas to form spinifex texture) is proposed to be a dominant effect on the viscosity during martian lava flow emplacement and

  3. Lunar Mare Basalts as Analogues for Martian Volcanic Compositions: Evidence from Visible, Near-IR, and Thermal Emission Spectroscopy

    NASA Technical Reports Server (NTRS)

    Graff, T. G.; Morris, R. V.; Christensen, P. R.

    2003-01-01

    The lunar mare basalts potentially provide a unique sample suite for understanding the nature of basalts on the martian surface. Our current knowledge of the mineralogical and chemical composition of the basaltic material on Mars comes from studies of the basaltic martian meteorites and from orbital and surface remote sensing observations. Petrographic observations of basaltic martian meteorites (e.g., Shergotty, Zagami, and EETA79001) show that the dominant phases are pyroxene (primarily pigeonite and augite), maskelynite (a diaplectic glass formed from plagioclase by shock), and olivine [1,2]. Pigeonite, a low calcium pyroxene, is generally not found in abundance in terrestrial basalts, but does often occur on the Moon [3]. Lunar samples thus provide a means to examine a variety of pigeonite-rich basalts that also have bulk elemental compositions (particularly low-Ti Apollo 15 mare basalts) that are comparable to basaltic SNC meteorites [4,5]. Furthermore, lunar basalts may be mineralogically better suited as analogues of the martian surface basalts than the basaltic martian meteorites because the plagioclase feldspar in the basaltic Martian meteorites, but not in the lunar surface basalts, is largely present as maskelynite [1,2]. Analysis of lunar mare basalts my also lead to additional endmember spectra for spectral libraries. This is particularly important analysis of martian thermal emission spectra, because the spectral library apparently contains a single pigeonite spectrum derived from a synthetic sample [6].

  4. Complex Formation History of Highly Evolved Basaltic Shergottite, Zagami

    NASA Technical Reports Server (NTRS)

    Niihara, T.; Misawa, K.; Mikouchi, T.; Nyquist, L. E.; Park, J.; Hirata, D.

    2012-01-01

    Zagami, a basaltic shergottite, contains several kinds of lithologies such as Normal Zagami consisting of Fine-grained (FG) and Coarse-grained (CG), Dark Mottled lithology (DML), and Olivine-rich late-stage melt pocket (DN). Treiman and Sutton concluded that Zagami (Normal Zagami) is a fractional crystallization product from a single magma. It has been suggested that there were two igneous stages (deep magma chamber and shallow magma chamber or surface lava flow) on the basis of chemical zoning features of pyroxenes which have homogeneous Mg-rich cores and FeO, CaO zoning at the rims. Nyquist et al. reported that FG has a different initial Sr isotopic ratio than CG and DML, and suggested the possibility of magma mixing on Mars. Here we report new results of petrology and mineralogy for DML and the Olivine-rich lithology (we do not use DN here), the most evolved lithology in this rock, to understand the relationship among lithologies and reveal Zagami s formation history

  5. Stratigraphy, composition and form of the Deccan Basalts, Western Ghats, India

    NASA Astrophysics Data System (ADS)

    Beane, J. E.; Turner, C. A.; Hooper, P. R.; Subbarao, K. V.; Walsh, J. N.

    1986-02-01

    In the Western Ghats between latitudes 18° 20' N and 19° 15' N, 7000 km2 of Deccan Basalt have been mapped with the primary objective of establishing a flow stratigraphy as a guide to the volcanic history of the flood basalts. Using over 70 measured vertical sections, major and trace element analyses of nearly 1200 samples, and rare-earth and87Sr/86Sr determinations for over 60 samples, we divide the basalt into three subgroups and ten formations. In this paper we describe the seven principal formations in the area and the most prominent individual flows. The Kalsubai Subgroup is formed by the lower five formations, the Jawhar, Igatpuri, Neral, Thakurvadi, and Bhimashankar formations, from botton to top. In these formations amygdaloidal compound flows predominate and have a typically high MgO content, including picrite basalt (> 10% MgO) and picrite (> 18% MgO) with phenocrysts of olivine and clinopyroxene. These flows are separated by others which contain giant plagioclase phenocrysts and have more evolved chamical compositions. The Lonavala Subgroup overlies the Kalsubai and is composed of two formations, the Khandala and the Bushe. Both are readily recognized in the field and by their chemical compositions. The Wai Subgroup includes the upper three formations, the Poladpur, the Ambenali, and the Mahabaleshwar. The whole subgroup is composed of simple flows with well-developed flow tops, small phenocrysts of plagioclase, pyroxene and olivine, and relatively evolved bulk compositions. Distribution and variation in thickness of the straitigraphic units within the Western Ghats provide a first comprehensive view of the development of the Deccan volcanic edifice. The persistent southerly dip and gentle southerly plunging anticlinal form of the flows, the lensoid shape of many of the formations, and nearly randomly oriented feeder-dike system are together interpreted as evidence of a central volcanic edifice formed as the Indian plate drifted northward over a mantle

  6. Amphibole-bearing multiphase solid inclusions in olivine, the Murotomisaki Gabbro, Southwest Japan: An evidence of hydrous flux melting

    NASA Astrophysics Data System (ADS)

    Hoshide, T.; Obata, M.

    2009-12-01

    The Murotomisaki Gabbro is a sill-like layered intrusion of up to 220m thickness exposed near Cape Muroto, Southwest Japan. Despite the small size of the intrusion, it contains well-developed centimeter- to meter-scale layered structures of modal variation of olivine, plagioclase and augite. Hoshide et al (2006a, b) identified the ’crystal accumulation zone’ (40m from the bottom) that was formed by gravitational settling of olivine crystals and the ’crystal growth zone’ (40-100m from the bottom), in which olivine crystals grew significantly. The fine-scale compositional layering is best developed in the ’crystal growth zone’. Amphibole-bearing multiphase solid inclusions (called ‘the amphibole-clot inclusions’) are common in olivine crystals from both the crystal accumulation- and the crystal growth zones. The amphibole clot inclusions show spherical or convex-polygonal shapes and are composed of pargasitic amphibole, biotite and orthopyroxene, with minor amounts of augite, apatite and opaque minerals. Plagioclase rarely occurs in the amphibole clot inclusions. Bulk chemical compositions of the inclusions, obtained from mineral microprobe analyses and modal composition, are characteristically high in MgO content (16-23 wt %) and they roughly lie between presumable fractionated melt compositions and olivine compositions. From observations above, it is likely that amphibole clot inclusions are of melt origin, which had formed from some hydrous melts probably entrapped in growing olivine crystals. However, it may be difficult to explain both the very magnesian nature of the inclusion and absence of plagioclase in the inclusion by the crystallization of the normal hydrous basaltic melt. The difficulty may be resolved if we suppose, for a trapped melt composition, a more magnesian (i.e., picritic) composition. The highly magnesian nature of the amphibole clot inclusions may suggest that significant amount of olivine component had been added to

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

    NASA Technical Reports Server (NTRS)

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

    2010-01-01

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

  8. The evolution and ascent paths of mantle xenolith-bearing magma: Observations and insights from Cenozoic basalts in Southeast China

    NASA Astrophysics Data System (ADS)

    Sun, Pu; Niu, Yaoling; Guo, Pengyuan; Cui, Huixia; Ye, Lei; Liu, Jinju

    2018-06-01

    Studies have shown that mantle xenolith-bearing magmas must ascend rapidly to carry mantle xenoliths to the surface. It has thus been inferred inadvertently that such rapid ascending melt must have undergone little crystallization or evolution. However, this inference is apparently inconsistent with the widespread observation that xenolith-bearing alkali basalts are variably evolved with Mg# ≤72. In this paper, we discuss this important, yet overlooked, petrological problem and offer new perspectives with evidence. We analyzed the Cenozoic mantle xenolith-bearing alkali basalts from several locations in Southeast China that have experienced varying degrees of fractional crystallization (Mg# = 48-67). The variably evolved composition of host alkali basalts is not in contradiction with rapid ascent, but rather reflects inevitability of crystallization during ascent. Thermometry calculations for clinopyroxene (Cpx) megacrysts give equilibrium temperatures of 1238-1390 °C, which is consistent with the effect of conductive cooling and melt crystallization during ascent because TMelt > TLithosphere. The equilibrium pressure (18-27 kbar) of these Cpx megacrysts suggests that the crystallization takes place under lithospheric mantle conditions. The host melt must have experienced limited low-pressure residence in the shallower levels of lithospheric mantle and crust. This is in fact consistent with the rapid ascent of the host melt to bring mantle xenoliths to the surface.

  9. Olivine on Earth

    NASA Image and Video Library

    2012-10-30

    The semi-precious gem peridot is a variety of olivine. NASA Curiosity rover shows the diffraction signature, or fingerprint, of the mineral olivine, shown here on Earth in the form of tumbled crystals.

  10. High-Mg subduction-related Tertiary basalts in Sardinia, Italy

    NASA Astrophysics Data System (ADS)

    Morra, V.; Secchi, F. A. G.; Melluso, L.; Franciosi, L.

    1997-03-01

    The Oligo-Miocene volcanics (32-15 Ma), which occur in the Oligo-Miocene Sardinian Rift, were interpreted in the literature as an intracontinental volcanic arc built upon continental crust about 30 km thick. They are characterized by a close field association of dominantly andesites and acid ignimbrites, with subordinate basalts. In this paper we deal with the origin and evolution of recently discovered high-magnesia basalts aged ca. 18 Ma occurring in the Montresta area, northern Sardinia, relevant to the petrogenesis of the Cenozoic volcanics of Sardinia. The igneous rocks of the Montresta area form a tholeiitic, subduction-related suite. Major-element variation from the high-magnesia basalts (HMB) to high-alumina basalts (HAB) are consistent with crystal/liquid fractionation dominated by olivine and clinopyroxene. Proportions of plagioclase and titanomagnetite increase from HAB to andesites. Initial {87Sr }/{86Sr } ratios increase with differentiation from 0.70398 for the HMB to 0.70592 for the andesites. This suggests concomitant crustal contamination. The geochemical characteristics of the high-magnesia basalts are typical of subduction-related magmas, with negative Nb, Zr and Ti spikes in mantle-normalized diagrams. It is proposed that these high-magnesia basalts were produced by partial melting of a mantle source characterized by large-ion lithophile elements (LILE) enrichment related principally to dehydration of subducted oceanic crust. Chondrite-normalized rare earth elements (REE) patterns indicate that the lavas are somewhat enriched in light rare earth elements (LREE), with flat heavy rare earth elements (HREE) patterns. This evidence is consistent with a spinel-bearing mantle source. The sub-parallel chondrite-normalized patterns show enrichment with differentiation, with a greater increase of LREE than HREE. The occurrence of high-magnesia basalts at 18 Ma in Sardinia appears to be correlated with and favoured by pronounced extensional tectonics at

  11. The Mineralogy of the Youngest Lunar Basalts

    NASA Astrophysics Data System (ADS)

    Staid, M. I.; Pieters, C. M.

    1999-01-01

    The last stage of lunar volcanism produced spectrally distinct basalts on the western nearside of the Moon, which remain unsampled by landing missions. The spectral properties of these late-stage basalts are examined using high-spatial-resolution Clementine images to constrain their mineralogic composition. The young high-Ti basalts in the western Procellarum and Imbrium Basins display a significantly stronger ferrous absorption than earlier mare basalts, suggesting that they may be the most Fe-rich deposits on the Moon. The distinct long-wavelength shape of this ferrous absorption is found to be similar for surface soils and materials excavated from depth. The pervasive character of this absorption feature supports the interpretation of abundant olivine within these late-stage lunar deposits. Important distinctions exist between the early-stage eastern maria and the late-stage western basalts, even though both appear to be Ti-rich. For example, the western maria are more radiogenic than eastern deposits. Telescopic spectra of the high-Ti western maria also exhibit a unique combination of a strong 1 micron feature and a relatively weak or attenuated 2-micron absorption. Pieters et al. concluded that the unusual strength and shape of the 1-micron absorption in western basalts results from an additional absorption from abundant olivine and/or Fe-bearing glass. Either mineralogy could produce the strong long wavelength 1-micron band, but a glassy Fe-rich surface could only form by rapid cooling along the exterior surfaces of flows. Clementine UV-VIS data of late-stage basalts are examined for regions in Oceanus Procellarum and Mare Imbrium. The spectral properties of western regions are compared to the sampled Apollo 11 basalts in Mare Tranquillitatis, which contain similar albedos and UV-VIS spectral properties. For reference, the western basalts are also compared to the low-Ti and Fe-rich basalts in Mare Serenitatis (mISP). Serenitatis basalts have the strongest

  12. Characterization and utilization potential of basalt rock from East-Lampung district

    NASA Astrophysics Data System (ADS)

    Isnugroho, K.; Hendronursito, Y.; Birawidha, D. C.

    2018-01-01

    The aim of this research was to study the petrography and chemical properties of basalt rock from East Lampung district, Lampung province. Petrography analysis was performed using a polarization microscope, and analysis of chemical composition using X-RF method. From the analysis of basalt rock samples, the mineral composition consists of pyroxene, plagioclase, olivine, and opaque minerals. Basic mass of basalt rock samples is, composed of plagioclase and pyroxene with subhedral-anhedral shape, forming intergranular texture, and uniform distribution. Mineral plagioclase is colorless and blade shape, transformed into opaque minerals with a size of <0.2 mm, whereas pyroxene present among the blades of plagioclase, with a greenish tint looked and a size of <0.006 mm. Mineral opaque has a rectangular shape to irregular, with a size of <0.16 mm. The chemical composition of basalt rock samples, consisting of 37.76-59.64 SiO2; 10.10-20.93 Fe2O3; 11.77-14.32 Al2O3; 5.57-14.75 CaO; 5.37-9.15 MgO; 1.40-3.34 Na2O. From the calculation, obtained the value of acidity ratio (Ma) = 3.81. With these values, indicate that the basalt rock from East Lampung district has the potential to be utilized as stone wool fiber.

  13. Petrogenesis of ultramafic rocks and olivine-rich troctolites from the East Taiwan Ophiolite in the Lichi mélange

    NASA Astrophysics Data System (ADS)

    Morishita, Tomoaki; Ghosh, Biswajit; Soda, Yusuke; Mizukami, Tomoyuki; Tani, Ken-ichiro; Ishizuka, Osamu; Tamura, Akihiro; Komaru, Chihiro; Aari, Shoji; Yang, Hsiao-Chin; Chen, Wen-Shan

    2017-12-01

    We examine ultramafic and olivine-rich troctolite blocks of the East Taiwan Ophiolite (ETO) in the Lichi Mélange. Although ultramafic rocks are extensively serpentinized, the primary minerals, such as olivine, orthopyroxene, clinopyroxene, spinel and plagioclase can be identified. The ultramafic rocks are classified into harzburgite (± clinopyroxene), dunite, and olivine websterite. Major and trace element compositions of the primary minerals in harzburgites, such as the Cr# [= Cr/(Cr + Al) atomic ratio] of chromian spinel (0.3-0.58) and incompatible elements-depleted trace element patterns of clinopyroxenes, indicate their residue origin after partial melting with less flux components. These compositions are similar to those from mid-ocean ridge peridotites as well as back-arc peridotites from the Philippine Sea Plate. The olivine websterite contains discrete as well as occasional locally concentrated plagioclase grains. Petrological characteristics coupled with similarity in trace element patterns of clinopyroxenes in the harzburgite and olivine websterite samples indicate that the olivine websterite is likely formed by clinopyroxene addition to a lherzolitic/harzburgitic peridotite from a pyroxene-saturated mafic melt. Dunite with medium Cr# spinels indicates cumulus or replacement by melt-peridotite reaction origins. Mineral composition of olivine-rich troctolite cannot be explained by simple crystallization from basaltic magmas, but shows a chemical trend expected for products after melt-peridotite interactions. Mineral compositions of the dunite and olivine-rich troctolite are also within chemical ranges of mid-ocean ridge samples, and are slightly different from back-arc samples from the Philippine Sea Plate. We conclude that peridotites in the ETO are not derived from the northern extension of the Luzon volcanic arc mantle. Further geochronological study is, however, required to constrain the origin of the ETO ophiolite, because peridotites are probably

  14. A Thermodynamic Approach for Modeling H2O-CO2 Solubility in Alkali-rich Mafic Magmas at Mid-crustal Pressures

    NASA Astrophysics Data System (ADS)

    Allison, C. M.; Roggensack, K.; Clarke, A. B.

    2017-12-01

    Volatile solubility in magmas is dependent on several factors, including composition and pressure. Mafic (basaltic) magmas with high concentrations of alkali elements (Na and K) are capable of dissolving larger quantities of H2O and CO2 than low-alkali basalt. The exsolution of abundant gases dissolved in alkali-rich mafic magmas can contribute to large explosive eruptions. Existing volatile solubility models for alkali-rich mafic magmas are well calibrated below 200 MPa, but at greater pressures the experimental data is sparse. To allow for accurate interpretation of mafic magmatic systems at higher pressures, we conducted a set of mixed H2O-CO2 volatile solubility experiments between 400 and 600 MPa at 1200 °C in six mafic compositions with variable alkali contents. Compositions include magmas from volcanoes in Italy, Antarctica, and Arizona. Results from our experiments indicate that existing volatile solubility models for alkali-rich mafic magmas, if extrapolated beyond their calibrated range, over-predict CO2 solubility at mid-crustal pressures. Physically, these results suggest that volatile exsolution can occur at deeper levels than what can be resolved from the lower-pressure experimental data. Existing thermodynamic models used to calculate volatile solubility at different pressures require two experimentally derived parameters. These parameters represent the partial molar volume of the condensed volatile species in the melt and its equilibrium constant, both calculated at a standard temperature and pressure. We derived these parameters for each studied composition and the corresponding thermodynamic model shows good agreement with the CO2 solubility data of the experiments. A general alkali basalt solubility model was also constructed by establishing a relationship between magma composition and the thermodynamic parameters. We utilize cation fractions from our six compositions along with four compositions from the experimental literature in a linear

  15. Internal Stratigraphy of the Palisades Sill Olivine Zone: An Olivine Slurry Emplaced in a Hot Sill

    NASA Astrophysics Data System (ADS)

    Haddad, J. R.; Naslund, H. R.

    2017-12-01

    The Palisades Sill is a 300 m thick Jurassic-Triassic sill-like sheet formed from a quartz-normative tholeiitic magma. Three geochemical reversals within the sill are the result of magma chamber recharges. This study focuses on the reversal at 10 m height, widely considered to be the result of the emplacement of an olivine-rich slurry (Husch 1990, Gorring 1995). Major and trace elements were determined for 35 samples from the olivine layer and adjacent sill spanning 10 m of stratigraphic height. Samples were collected from outcrops near the Ross Dock Picnic Area in Fort Lee, NJ. Mineral compositions were determined for 21 thin sections using an electron microprobe (EMP). Bulk rock chemistry shows that the base of the olivine layer is between 2.5 and 3.25 m above the base of sampling. This is indicated by a marked reversal in Mg#, which jumped from 64.2 to 68.6; Al2O3, Co, Ni, Sc, Cs, Dy, and La also show clear reversals at the same interval. This is further collaborated by the formation of a ledge in the outcrop. Bulk chemistry and olivine composition show no systematic changes within the olivine layer. EMP analyses of augites reveals that below the 2.5 m height, crystals are typically strongly zoned, average rim Mg#= 67, core Mg#= 82. Above the 2.5 m layer, core Mg# are similar, but average rim Mg#=75. The plagioclase/augite ratio remains relatively constant through the olivine layer, but the ratio of olivine to plagioclase+augite is quite variable, suggesting that the olivine-slurry was emplaced as an inhomogeneous mixture of olivine + magma. Similar tholeiitic sills on Victoria Island, Canada, contain olivine-rich basal layers in which the olivine to plagioclase+augite ratio systematically increases, and the olivine composition becomes systematically more Fe-rich, from the base to the top of the layer. Comparisons between these otherwise similar basal olivine-rich layers, suggests that sills like the Palisades, which represents the injection of an olivine

  16. Mineralogy as a function of depth in the prehistoric Makaopuhi tholeiitic lava lake, Hawaii

    USGS Publications Warehouse

    Evans, B.W.; Moore, J.G.

    1968-01-01

    The electron probe X-ray microanalyzer has been used to determine the compositional variability of the groundmass minerals and glass in 10 specimens from a complete 225-foot section of the prehistoric tholeiitic lava lake of Makaopuhi Crater, Hawaii. The order of beginning of crystallization was: (1) chromite, (2) olivine, (3) augite, (4) plagioclase, (5) pigeonite, (6) iron-titanium oxides and orthopyroxene, (7) alkali feldspar and apatite, and (8) glass. Although the lake is chemically tholeiitic throughout, the occurrence of ferromagnesian minerals is as though there were a gradation from alkali olivine basalt in the upper chill downwards to olivine tholeiite. Groundmass olivine decreases downwards and disappears at about 20 feet. Pigeonite is absent in the uppermost 5??2 feet, then increases in amount down to 20 feet, below which augite and pigeonite coexist in constant 2:1 proportions. Strong zoning and metastable compositions characterize the pyroxenes of the chilled zones, but these features gradually disappear towards the interior of the lake to give way to equilibrium pyroxenes. Relatively homogeneous poikilitic orthopyroxene (??? Ca4Mg70Fe26) occurs in the olivine cumulate zone, having formed partly at the expense of pre-existing olivine, augite, and pigeonite (??? Ca8Mg66Fe26). The growth of orthopyroxene is believed to have been facilitated by the slower cooling rate and higher volatile pressure at depth, and by the rise in Mg/Fe ratio of the liquid due to the partial dissolution of settled olivine. Unlike olivine and pyroxene, feldspar is least zoned in the upper and lower chilled regions. The greatest range of compositional zoning in feldspar occurs at 160 to 190 feet, where it extends continuously from Or1.0Ab22An77 to Or64Ab33An3. The feldspar fractionation trend in the An-Ab-Or triangle gradually shifts with depth toward more "equilibrium" trends, even though the zoning becomes more extreme. The variation with depth in the initial (core

  17. Genomic evidence for the Wood-Ljungdahl pathway for carbon fixation in warm basaltic ocean crust

    NASA Astrophysics Data System (ADS)

    Smith, A. R.; Fisk, M. R.; Mueller, R.; Colwell, F. S.; Mason, O. U.; Popa, R.

    2016-12-01

    Microbial life in the deep suboceanic aquifer can harness geochemical energy resulting from water-rock reactions and contribute to carbon cycling in the ocean via primary production, or chemosynthesis. Iron-bearing minerals such as olivine in oceanic crust can produce molecular hydrogen, small molecular weight hydrocarbons, and hydrogen sulfide as they react with seawater. Although this generally occurs in serpentinizing systems at very high temperatures deep in the subsurface, it has also been hypothesized to drive the subseafloor microbial ecosystems present in shallower basaltic aquifers. We present genome-based evidence for chemolithoautotrophic microbes present on the surface of olivine incubated in Juan de Fuca Ridge basaltic ocean crust for a 4-year period. These metagenome-derived genomes show dominant taxa capable of using both branches of the Wood-Ljungdahl pathway for carbon fixation and energy generation. This pathway uses molecular hydrogen potentially derived from the olivine surface as it reacts with seawater and CO2 which is inherent to seawater. These taxa were not reported from aquifer fluid samples, but have been found only in association with mineral surfaces in this study location. Most taxa in this simple community are distant relatives of cultured taxa; therefore this genome information is crucial to understanding how the subseafloor aquifer community is structured, how it obtains energy, how it cycles carbon, and gives us keys to help cultivate these organisms in the laboratory. Our findings also support the Subsurface Lithoautotrophic Microbial Ecosystem (SLiME) hypothesis and have implications for understanding life on early Earth and the potential for life in the Martian subsurface.

  18. Crustal accretion along the global mid-ocean ridge system based on basaltic glass and olivine-hosted melt inclusion compositions

    NASA Astrophysics Data System (ADS)

    Wanless, V. D.; Behn, M. D.

    2015-12-01

    The depth and distribution of crystallization at mid-ocean ridges controls the overall architecture of the oceanic crust, influences hydrothermal circulation, and determines geothermal gradients in the crust and uppermost mantle. Despite this, there is no overall consensus on how crystallization is distributed within the crust/upper mantle or how this varies with spreading rate. Here, we examine crustal accretion at mid-ocean ridges by combining crystallization pressures calculated from major element barometers on mid-ocean ridge basalt (MORB) glasses with vapor-saturation pressures from melt inclusions to produce a detailed map of crystallization depths and distributions along the global ridge system. We calculate pressures of crystallization from >11,500 MORB glasses from the global ridge system using two established major element barometers (1,2). Additionally, we use vapor-saturation pressures from >400 olivine-hosted melt inclusions from five ridges with variable spreading rates to constrain pressures and distributions of crystallization along the global ridge system. We show that (i) crystallization depths from MORB glasses increase and become less focused with decreasing spreading rate, (ii) maximum glass pressures are greater than the maximum melt inclusion pressure, which indicates that the melt inclusions do not record the deepest crystallization at mid-ocean ridges, and (iii) crystallization occurs in the lower crust/upper mantle at all ridges, indicating accretion is distributed throughout the crust at all spreading rates, including those with a steady-state magma lens. Finally, we suggest that the remarkably similar maximum vapor-saturation pressures (~ 3000 bars) in melt inclusion from all spreading rates reflects the CO2 content of the depleted upper mantle feeding the global mid-ocean ridge system. (1) Michael, P. & W. Cornell (1998), Journal of Geophysical Research, 103(B8), 18325-18356; (2) Herzberg, C. (2004), Journal of Petrology, 45(12), 2389.

  19. Timing and composition of continental volcanism at Harrat Hutaymah, western Saudi Arabia

    USGS Publications Warehouse

    Duncan, Robert A.; Kent, Adam J R; Thornber, Carl; Schliedler, Tyler D; Al-Amri, Abdullah M

    2016-01-01

    Harrat Hutaymah is an alkali basalt volcanic field in north-central Saudi Arabia, at the eastern margin of a large Neogene continental, intraplate magmatic province. Lava flow, tephra and spatter cone compositions in the field include alkali olivine basalts and basanites. These compositions contrast with the predominantly tholeiitic, fissure-fed basalts found along the eastern margin of the Red Sea. The Hutaymah lava flows were erupted through Proterozoic arc-associated plutonic and meta-sedimentary rocks of the Arabian shield, and commonly contain a range of sub-continental lithospheric xenoliths, although the lavas themselves show little indication of crustal contamination. Previous radiometric dating of this volcanic field (a single published K–Ar age; 1.8 Ma) is suspiciously old given the field measurement of normal magnetic polarity only (i.e. Brunhes interval, ≤ 780 Ka). We report new age determinations on 14 lava flows by the 40Ar–39Ar laser step heating method, all younger than ~ 850 Ka, to better constrain the time frame of volcanism, and major, trace and rare earth element compositions to describe the chemical variation of volcanic activity at Harrat Hutaymah. Crystal fractionation was dominated by olivine ± clinopyroxene at a range of upper mantle and crustal pressures. Rapid ascent and eruption of magma is indicated by the array of lower crustal and lithospheric xenoliths observed in lava flows and tephra. Modeling suggests 1–7% melting of an enriched asthenospheric mantle source occurred beneath Harrat Hutaymah under a relatively thick lithospheric cap (60–80 km).

  20. Timing and composition of continental volcanism at Harrat Hutaymah, western Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Duncan, Robert A.; Kent, Adam J. R.; Thornber, Carl R.; Schlieder, Tyler D.; Al-Amri, Abdullah M.

    2016-03-01

    Harrat Hutaymah is an alkali basalt volcanic field in north-central Saudi Arabia, at the eastern margin of a large Neogene continental, intraplate magmatic province. Lava flow, tephra and spatter cone compositions in the field include alkali olivine basalts and basanites. These compositions contrast with the predominantly tholeiitic, fissure-fed basalts found along the eastern margin of the Red Sea. The Hutaymah lava flows were erupted through Proterozoic arc-associated plutonic and meta-sedimentary rocks of the Arabian shield, and commonly contain a range of sub-continental lithospheric xenoliths, although the lavas themselves show little indication of crustal contamination. Previous radiometric dating of this volcanic field (a single published K-Ar age; 1.8 Ma) is suspiciously old given the field measurement of normal magnetic polarity only (i.e. Brunhes interval, ≤ 780 Ka). We report new age determinations on 14 lava flows by the 40Ar-39Ar laser step heating method, all younger than ~ 850 Ka, to better constrain the time frame of volcanism, and major, trace and rare earth element compositions to describe the chemical variation of volcanic activity at Harrat Hutaymah. Crystal fractionation was dominated by olivine ± clinopyroxene at a range of upper mantle and crustal pressures. Rapid ascent and eruption of magma is indicated by the array of lower crustal and lithospheric xenoliths observed in lava flows and tephra. Modeling suggests 1-7% melting of an enriched asthenospheric mantle source occurred beneath Harrat Hutaymah under a relatively thick lithospheric cap (60-80 km).

  1. Genetic interpretation of lead-isotopic data from the Columbia River basalt group, Oregon, Washington, and Idaho.

    USGS Publications Warehouse

    Church, S.E.

    1985-01-01

    Lead-isotopic data for the high-alumina olivine plateau basalts and most of the Colombia River basalt group plot within the Cascade Range mixing array. The data for several of the formations form small, tight clusters and the Nd and Sr isotopic data show discrete variation between these basalt groups. The observed isotopic and trace-element data from most of the Columbia River basalt group can be accounted for by a model which calls for partial melting of the convecting oceanic-type mantle and contamination by fluids derived from continental sediments which were subducted along the trench. These sediments were transported in the low-velocity zone at least 400 km behind the active arc into a back-arc environment represented by the Columbia Plateau province. With time, the zone of melting moved up, resulting in the formation of the Saddle Mt basalt by partial melting of a 2600 m.y.-old sub-continental lithosphere characterized by high Th/U, Th/Pb, Rb/Sr and Nd/Sm ratios and LREE enrichment. Partial melting of old sub-continental lithosphere beneath the continental crust may be an important process in the formation of continental tholeiite flood basalt sequences world-wide. -L.di H.

  2. Disequilibrium growth of olivine in mafic magmas revealed by phosphorus zoning patterns of olivine from mafic-ultramafic intrusions

    NASA Astrophysics Data System (ADS)

    Xing, Chang-Ming; Wang, Christina Yan; Tan, Wei

    2017-12-01

    Olivine from mafic-ultramafic intrusions rarely displays growth zoning in major and some minor elements, such as Fe, Mg and Ni, due to fast diffusion of these elements at high temperatures. These elements in olivine are thus not useful in deciphering magma chamber processes, such as magma convection, multiple injection and mixing. High-resolution X-ray elemental intensity mapping reveals distinct P zoning patterns of olivine from two mafic-ultramafic intrusions in SW China. Polyhedral olivine grains from lherzolite and dunite of the Abulangdang intrusion show P-rich dendrites similar to those observed in volcanic rocks. Rounded olivine grains from net-textured Fe-Ti oxide ores of the Baima layered intrusion have irregular P-rich patches/bands crosscut and interlocked by P-poor olivine domains. P-rich patches/bands contain 250 to 612 ppm P, much higher than P-poor olivine domains with 123 to 230 ppm P. In electron backscattered diffraction (EBSD) maps, P-rich patches/bands within a single olivine grain have the same crystallographic orientation, indicating that they were remnants of the same crystal. Thus, both P-rich patches/bands and P-poor olivine domains in the same grain show a disequilibrium texture and clearly record two-stage growth. The P-rich patches/bands are likely the remnants of a polyhedral olivine crystal that formed in the first stage, whereas the P-poor olivine domains containing rounded Ti-rich magnetite and Fe-rich melt inclusions may have formed from an Fe-rich ambient melt in the second stage. The complex P zoning of olivine can be attributed to the dissolution of early polyhedral olivine and re-precipitation from the Fe-rich ambient melt. The early polyhedral olivine was in chemical disequilibrium with the ambient melt that may have been developed by silicate liquid immiscibility in a crystal mush. Our study implies that olivine crystals in igneous cumulates with an equilibrium appearance may have experienced disequilibrium growth processes

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

    NASA Astrophysics Data System (ADS)

    Ntaflos, Theodoros; Abart, Rainer; Bizimis, Michel

    2017-04-01

    inclusions in second generation clinopyroxene within the melt pockets. Evidently the melt pockets represent amphibole, which have been incongruently molten. The necessary heat for the amphibole breakdown was derived from the host basalt. The estimated time for diffusive Ca exchange between matrix olivine and olivine overgrowth in contact with the melt pockets is very short, ranging between 21 and 200 days, indicating that amphibole breakdown took place immediately before or during the xenolith entrainment in the alkali basalt.

  4. Experimental Melting Study of Basalt-Peridotite Hybrid Source: Constrains on Chemistry of Recycled Component

    NASA Astrophysics Data System (ADS)

    Gao, S.; Takahashi, E.; Matsukage, K. N.; Suzuki, T.; Kimura, J. I.

    2015-12-01

    It is believed that magma genesis of OIB is largely influenced by recycled oceanic crust component involved in the mantle plume (e.g., Hauri et al., 1996; Takahashi & Nakajima., 2002; Sobolev et al., 2007). Mallik & Dasgupta (2012) reported that the wall-rock reaction in MORB-eclogite and peridotite layered experiments produced a spectrum of tholeiitic to alkalic melts. However, the proper eclogite source composition is still under dispute. In order to figure out the geochemistry of recycled component as well as their melting process, we conducted a series of high-P, high-T experiments. Melting experiments (1~10hrs) were performed under 2.9GPa with Boyd-England type piston-cylinder (1460~1540°C for dry experiments, 1400~1500°C for hydrous experiments) and 5GPa with Kawai-type multi-anvil (1550~1650°C for dry experiments, 1350~1550°C for hydrous experiments), at the Magma Factory, Tokyo Tech. Spinel lherzolite KLB-1 (Takahashi 1986) was employed as peridotite component. Two basalts were used as recycled component: Fe-enriched Columbia River basalt (CRB72-180, Takahashi et al., 1998) and N-type MORB (NAM-7, Yasuda et al., 1994). In dry experiments below peridotite dry solidus, melt compositions ranged from basaltic andesite to tholeiite. Opx reaction band generated between basalt and peridotite layer hindered chemical reaction. On the other hand, alkali basalt was formed in hydrous run products because H2O promoted melting process in both layers. Compared with melts formed by N-MORB-peridotite runs, those layered experiments with CRB are enriched in FeO, TiO2, K2O and light REE at given MgO. In other words, melts produced by CRB-peridotite layered experiments are close to alkali basalts in OIB and tholeiite in Hawaii, while those by layered experiments with N-MORB are poor in above elements. Thus we propose that Fe-rich Archean or Proterozoic tholeiite (BVSP 1980) would be a possible candidate for recycled component in OIB source.

  5. Ar-40/Ar-39 Ages for Maskelynites and K-Rich Melt from Olivine-Rich Lithology in (Kanagawa) Zagami

    NASA Technical Reports Server (NTRS)

    Park, J.; Herzog, G. F.; Nyquist, L. E.; Lindsay, F.; Turrin, B.; Swisher, C. C., III; Delaney, J. S.; Shih, C.-Y.; Niihara, T.; Misawa, K.

    2013-01-01

    We report Ar/Ar release patterns for small maskelynite grains and samples of a K-rich phase separated from the basaltic shergottite Zagami. The purpose of the work is to investigate the well-known discrepancy between published Ar/Ar ages of Zagami, >200 Ma, and its age of approx. 170 Ma as determined by other methods [1-6]. Niihara et al. [7] divide less abundant darker material present in Zagami into an olivine-rich lithology (ORL), from which most of our samples came, and a pyroxene-rich one (Dark Mottled-Lithology: DML) [8, 9]. ORL consists of vermicular fayalitic olivine, coarse-grained pyroxene, maskelynite, and a glassy phase exceptionally rich in K (up to 8.5 wt%), Al, and Si, but poor in Fe and Mg. The elemental composition suggests a late-stage melt, i.e., residual material that solidified late in a fractional crystallization sequence. Below we refer to it as "K-rich melt." The K-rich melt contains laths of captured olivine, Ca-rich pyroxene, plagioclase, and opaques. It seemed to offer an especially promising target for Ar-40/Ar-39 dating.

  6. Sulfides from Martian and Lunar Basalts: Comparative Chemistry for Ni Co Cu and Se

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

    J Papike; P Burger; C Shearer

    2011-12-31

    Here Mars and Moon are used as 'natural laboratories' with Moon displaying lower oxygen fugacities ({approx}IW-1) than Mars ({approx}IW to FMQ). Moon has lower concentrations of Ni and Co in basaltic melts than does Mars. The major sulfides are troilite (FeS) in lunar basalts and pyrrhotite (Fe{sub 1-x}S) in martian basalts. This study focuses on the concentrations of Ni, Co, Cu, and Se. We chose these elements because of their geochemical importance and the feasibility of analyzing them with a combination of synchrotron X-ray fluorescence (SXRF) and electron microprobe (EPMA) techniques. The selenium concentrations could only be analyzed, at highmore » precision, with SXRF techniques as they are <150 ppm, similar to concentrations seen in carbonaceous chondrites and interplanetary dust particles (IDPs). Nickel and Co are in higher concentrations in martian sulfides than lunar and are higher in martian olivine-bearing lithologies than olivine-free varieties. The sulfides in individual samples show very large ranges in concentration (e.g., Ni ranges from 50 000 ppm to <5 ppm). These large ranges are mainly due to compositional heterogeneities within individual grains due to diffusion and phase separation. Electron microprobe wavelength-dispersive (WDS) mapping of Ni, Co, and Cu show the diffusion trajectories. Nickel and Co have almost identical diffusion trajectories leading to the likely nucleation of pentlandite (Ni,Co,Fe){sub 9}S{sub 8}, and copper diffuses along separate pathways likely toward chalcopyrite nucleation sites (CuFeS{sub 2}). The systematics of Ni and Co in lunar and martian sulfides clearly distinguish the two parent bodies, with martian sulfides displaced to higher Ni and Co values.« less

  7. Quaternary basaltic volcanism in the Golden Trout Volcanic Field, southern Sierra Nevada, California

    NASA Astrophysics Data System (ADS)

    Browne, Brandon L.; Becerra, Raul; Campbell, Colin; Saleen, Phillip; Wille, Frank R.

    2017-09-01

    The Golden Trout Volcanic Field (GTVF) produced the only Quaternary eruptions of mafic magma within the southern Sierra Nevada block. Approximately 38 × 106 m3 of basalt, trachy-basalt, basaltic trachy-andesite, and basaltic andesite (50.1-56.1% SiO2, 1.1-1.9% K2O, and 5.4-9.1% MgO) was erupted from four vents within a 10 km2 portion of the GTVF, which also includes rhyolite domes that are not considered in this study. The vents include, from oldest to youngest: Little Whitney Cone, South Fork Cone, Tunnel Cone, and unglaciated Groundhog Cone. Little Whitney Cone is a 120 m-high pile of olivine-CPX-phyric scoria produced during a Strombolian-style eruption overlying two columnar jointed lava flows. Tunnel Cone formed through a Hawaiian-style eruption along a 400 m-long north-south trending fissure that excavated at least three 25-65 m-wide craters. Crater walls up to 12 m high are composed of plagioclase-olivine-phyric spatter-fed flows that dip radially away from the crater center and crumble to form Tunnel Cone's steep unconsolidated flanks. South Fork Cone is a 170 m-high pile of plagioclase-olivine-phyric scoria that formed during Strombolian to violent Strombolian eruptions. South Fork Cone overlies the South Fork Cone lava, a 9.5 km-long flow ( 12 × 106 km3) that reached the Kern River Canyon to the west. Scoria and airfall deposits originating from South Fork Cone are located up to 2 km from the vent. Groundhog Cone is a 140 m-tall cinder and spatter cone breached on the north flank by a 13 × 106 m3 lava flow that partially buried the South Fork Cone lava and extends 7.5 km west to Kern River Canyon. Incompatible trace element concentrations and ratios show vent-specific trends but are unsystematic when plotted in terms of all mafic GTVF vents, implying that GTVF basalts were derived from a lithospheric mantle source and ascended through thick granitic Sierra Nevada crust as discrete batches that underwent different degrees of crustal contamination

  8. Sm-Nd and Rb-Sr Isotopic Studies of Meteorite Kalahari 009: An Old VLT Mare Basalt

    NASA Technical Reports Server (NTRS)

    Shih, C.-Y.; Nyquist, L. E.; Reese, Y.; Bischoff, A.

    2008-01-01

    Lunar meteorite Kalahari 009 is a fragmental basaltic breccia contain ing various very-low-Ti (VLT) mare basalt clasts embedded in a fine-g rained matrix of similar composition. This meteorite and lunar meteorite Kalahari 008, an anorthositic breccia, were suggested to be paired mainly due to the presence of similar fayalitic olivines in fragment s found in both meteorites. Thus, Kalahari 009 probably represents a VLT basalt that came from a locality near a mare-highland boundary r egion of the Moon, as compared to the typical VLT mare basalt samples collected at Mare Crisium during the Luna-24 mission. The concordant Sm-Nd and Ar-Ar ages of such a VLT basalt (24170) suggest that the extrusion of VLT basalts at Mare Crisium occurred 3.30 +/- 0.05 Ga ag o. Previous age results for Kalahari 009 range from approximately 4.2 Ga by its Lu-Hf isochron age to 1.70?0.04 Ga of its Ar-Ar plateau ag e. However, recent in-situ U-Pb dating of phosphates in Kalahari 009 defined an old crystallization age of 4.35+/- 0.15 Ga. The authors su ggested that Kalahari 009 represents a cryptomaria basalt. In this r eport, we present Sm-Nd and Rb-Sr isotopic results for Kalahari 009, discuss the relationship of its age and isotopic characteristics to t hose of other L-24 VLT mare basalts and other probable cryptomaria ba salts represented by Apollo 14 aluminous mare basalts, and discuss it s petrogenesis.

  9. Processes and time scales of magmatic evolution as revealed by Fe-Mg chemical and isotopic zoning in natural olivines

    NASA Astrophysics Data System (ADS)

    Oeser, Martin; Dohmen, Ralf; Horn, Ingo; Schuth, Stephan; Weyer, Stefan

    2015-04-01

    In this study, we applied high-precision in situ Fe and Mg isotope analyses by femtosecond laser ablation (fs-LA) MC-ICP-MS on chemically zoned olivine xeno- and phenocrysts from intra-plate volcanic regions in order to investigate the magnitude of Fe and Mg isotope fractionation and its suitability to gain information on magma evolution. Our results show that chemical zoning (i.e., Mg#) in magmatic olivines is commonly associated with significant zoning in δ56Fe and δ26Mg (up to 1.7‰ and 0.7‰, respectively). We explored different cases of kinetic fractionation of Fe and Mg isotopes by modeling diffusion in the melt or olivine and simultaneous growth or dissolution. Combining the information of chemical and isotopic zoning in olivine allows to distinguish between various processes that may occur during magma evolution, namely diffusive Fe-Mg exchange between olivine and melt, rapid crystal growth, and Fe-Mg inter-diffusion simultaneous to crystal dissolution or growth. Chemical diffusion in olivine appears to be the dominant process that drives isotope fractionation in magmatic olivine. Simplified modeling of Fe and Mg diffusion is suitable to reproduce both the chemical and the isotopic zoning in most of the investigated olivines and, additionally, provides time information about magmatic processes. For the Massif Central (France), modeling of diffusive re-equilibration of mantle olivines in basanites revealed a short time span (<2 years) between the entrainment of a mantle xenolith in an intra-plate basaltic magma and the eruption of the magma. Furthermore, we determined high cooling rates (on the order of a few tens to hundreds of °C per year) for basanite samples from a single large outcrop in the Massif Central, which probably reflects the cooling of a massive lava flow after eruption. Results from the modeling of Fe and Mg isotope fractionation in olivine point to a systematic difference between βFe and βMg (i.e., βFe/βMg ≈ 2), implying that the

  10. Olivine-bearing lithologies on the Moon: Constraints on origins and transport mechanisms from M3 spectroscopy, radiative transfer modeling, and GRAIL crustal thickness

    NASA Astrophysics Data System (ADS)

    Corley, Laura M.; McGovern, Patrick J.; Kramer, Georgiana Y.; Lemelin, Myriam; Trang, David; Gillis-Davis, Jeffrey J.; Taylor, G. Jeffrey; Powell, Kathryn E.; Kiefer, Walter S.; Wieczorek, Mark; Zuber, Maria T.

    2018-01-01

    High-resolution hyperspectral data from Chandrayaan-1's Moon Mineralogy Mapper (M3) allow detection of olivine on the lunar surface. Olivine exposed at the surface may originate as mantle material or igneous products (intrusive or extrusive). Potential transport mechanisms include excavation of the mantle or lower crustal material by impacts that form basins and complex craters, differentiation of impact melt sheets, or magmatic emplacement of lavas, cumulates, or xenoliths. A sample of the lunar mantle, which has not been conclusively identified in the lunar sample collection, would yield fundamental new insights into the composition, structure, and evolution of the lunar interior. Olivine identified in remote spectral data is generally accepted to originate from the primary mantle, because abundant olivine is expected to exist in the mantle and lower crust, yet have sparse occurrences in the upper crust. In this study, we identified 111 M3 single-pixel spectra with characteristic absorption features consistent with olivine at Crisium, Nectaris, and Humorum basins and near the craters Roche and Tsiolkovsky. In an effort to determine the origins and transport mechanisms that led to these individual exposures, we estimated mineral abundances using radiative transfer modeling and examined crustal thickness estimates, topography and slope maps, and images from the Lunar Reconnaissance Orbiter Camera (LROC). At Crisium basin, where crustal thickness is near 0 km (Wieczorek et al., 2013), mantle olivine may have been exposed by basin-forming impact and deposited on the rim. Picard crater, which is superposed on the floor of Crisium, also exhibits potential mantle olivine in its ejecta. Within Nectaris basin, olivine exposures are confined to the rims of small craters on the mare, which are inferred to excavate a layer of olivine-rich mare basalt. Olivine occurrences on the rim of Humorum basin, including those located on a graben, are likely to be cumulates of shallow

  11. Raman and FTIR spectroscopy of methane in olivine

    NASA Astrophysics Data System (ADS)

    Smith, A.; Oze, C.; Rossman, G. R.; Celestian, A. J.

    2017-12-01

    Olivine has been proposed to be a direct source of methane (CH4) in serpentinization systems and experiments. Here, Raman and Fourier Transform Infrared (FTIR) spectroscopy were used to verify the presence and abundance of CH4 in olivine samples from nine localities, including the San Carlos olivine. Raman analyses did not identify any methane in the olivine samples. As olivine is orthorhombic, three polarized FTIR spectra were obtained for the olivine samples. No methane was detected in any of the olivine samples using FTIR. Overall, olivine investigated in this study does not appear to be a primary source of methane.

  12. Crystallization of tholeiitic basalt in Alae Lava Lake, Hawaii

    USGS Publications Warehouse

    Peck, D.L.; Wright, T.L.; Moore, J.G.

    1966-01-01

    The eruption of Kilauea Volcano August 21-23, 1963, left 600,000 cubic meters of basaltic lava in a lava lake as much as 15 meters deep in Alae pit crater. Field studies of the lake began August 27 and include repeated core drilling, measurements of temperature in the crust and melt, and precise level surveys of the lake surface. The last interstitial melt in the lake solidified late in September 1964; by mid August 1965 the maximum temperature was 690??C at a depth of 11.5 meters. Pumice air-quenched from about 1140??C contains only 5 percent crystals - clinopyroxene, cuhedral olivine (Fo 80), and a trace of plagioclase, (An 70). Drill cores taken from the zone of crystallization in the lake show that olivine continued crystallizing to about 1070??C; below that it reacts with the melt, becoming corroded and mantled by pyroxene and plagioclase. Below 1070??C, pyroxene and plagioclase crystallized at a constant ratio. Ilmenite first appeared at about 1070??C and was joined by magnetite at about 1050??C; both increased rapidly in abundance to 1000??C. Apatite first appeared as minute needles in interstitial glass at 1000??C. Both the abundance and index of refraction of glass quenched from melt decreased nearly linearly with falling temperature. At 1070??C the quenched lava contains about 65 percent dark-brown glass with an index of 1.61; at 980??C it contains about 8 percent colorless glass with an index of 1.49. Below 980??C, the percentage of glass remained constant. Progressive crystallization forced exsolution of gases from the melt fraction; these formed vesicles and angular pores, causing expansion of the crystallizing lava and lifting the surface of the central part of the lake an average of 19.5 cm. The solidified basalt underwent pneumatolitic alteration, including deposition of cristobalite at 800??C, reddish alteration of olivine at 700??C, tarnishing of ilmenite at 550??C, deposition of anhydrite at 250??C, and deposition of native sulfur at 100??C

  13. CO2 and H2O Contents of Melt Inclusions from the 1891 Basaltic Balloon Eruption of Foerstner Submarine Volcano, Italy

    NASA Astrophysics Data System (ADS)

    Balcanoff, J. R.; Carey, S.; Kelley, K. A.; Boesenberg, J. S.

    2016-12-01

    Eruptions that produce basaltic balloon products are an uncommon eruption style only observed in five cases during historical times. Basaltic balloon products form in gas rich shallow submarine eruptions, which produce large hollow clasts with sufficient buoyancy to float on seawater. Foerstner submarine volcano, off the coast of Pantelleria (Italy), erupted with this style in 1891 and is the only eruption where the vent site (250 m water depth) has been studied and sampled in detail with remotely operated vehicles (ROVs). Here, we report Fournier Transform Infrared Spectroscopy (FTIR) and electron microprobe (EMP) analyses of major elements and dissolved volatiles in melt inclusions from olivine and plagioclase phenocrysts picked from highly vesicular clasts recovered from the seafloor. The trachybasaltic melt is enriched in alkalis with notably high phosphorus (1.82-2.38 wt%), and melt inclusions show elevated H2O concentrations of 0.17 to 1.2 wt.% and highly elevated CO2 concentrations of 928 to 1864 ppm. Coexisting matrix glass is completely degassed with respect to carbon dioxide but has variable water contents up to 0.19 %. The maximum carbon dioxide value implies saturation at 1.5 kb, or 4.5 km below the volcano. Trends in the CO2 and H2O data are most compatible with calculated open system degassing behavior. This is consistent with a proposed balloon formation mechanism involving a hybrid strombolian eruption style with the potential accumulation of gas-rich pockets below the vent as gas bubbles moved upwards independent of the low viscosity basaltic melt. Discharge of the gas-rich pockets led to the discharge of meter-sized slugs of magma with large internal vesicles (several tens of centimeters). A subset of these clasts had bulk densities that were lower than seawater, allowing them to rise to the sea surface where they either exploded or became water saturated and sank back to the seafloor.

  14. Mineralogical Comparison of Olivine in Shergottites and A Shocked L Chondrite: Implications for Shock Histories of Brown Olivine

    NASA Technical Reports Server (NTRS)

    Takenouchi, A.; Mikouchi, T.; Yamaguchi, A.; Zolensky, M. E.

    2015-01-01

    Most Martian meteorites are heavily shocked, exhibiting numerous shock features, for example undulatory extinction of olivine and pyroxene, the presence of diaplectic glass ("maskelynite") and the formation of shock melt. Among these shock features, olivine darkening ("brown" olivine) is unique in Martian meteorites because no other meteorite group shows such a feature. Although the presence of brown olivine in shergottites was reported thirty years ago, detailed observation by TEM has not been performed until the NWA 2737 chassignite was discovered, whose olivine is darkened, being completely black in hand specimen. Fe metal nano-particles were found in NWA 2737 olivine which are considered to have been formed by olivine reduction during heavy shock. Subsequently, magnetite nano-particles were also found in other Martian meteorites and the coexistence of Fe metal and magnetite nano-particles was reported in the NWA 1950 shergottite and some Fe metal nano-particles were mantled by magnetite. Therefore, the formation process of nano-particles seems to be complex. Because "brown" olivine is unique to Martian meteorites, they have a potential to constrain their shock conditions. In order to better understand the shock history of Martian meteorites, we compared olivine in several shergottites with that in a highly-shocked L chondrite which contains ringwoodite.

  15. The ascent of kimberlite: Insights from olivine

    NASA Astrophysics Data System (ADS)

    Brett, R. C.; Russell, J. K.; Andrews, G. D. M.; Jones, T. J.

    2015-08-01

    Olivine xenocrysts are ubiquitous in kimberlite deposits worldwide and derive from the disaggregation of mantle-derived peridotitic xenoliths. Here, we provide descriptions of textural features in xenocrystic olivine from kimberlite deposits at the Diavik Diamond Mine, Canada and at Igwisi Hills volcano, Tanzania. We establish a relative sequence of textural events recorded by olivine during magma ascent through the cratonic mantle lithosphere, including: xenolith disaggregation, decompression fracturing expressed as mineral- and fluid-inclusion-rich sealed and healed cracks, grain size and shape modification by chemical dissolution and abrasion, late-stage crystallization of overgrowths on olivine xenocrysts, and lastly, mechanical milling and rounding of the olivine cargo prior to emplacement. Ascent through the lithosphere operates as a "kimberlite factory" wherein progressive upward dyke propagation of the initial carbonatitic melt fractures the overlying mantle to entrain and disaggregate mantle xenoliths. Preferential assimilation of orthopyroxene (Opx) xenocrysts by the silica-undersaturated carbonatitic melt leads to deep-seated exsolution of CO2-rich fluid generating buoyancy and supporting rapid ascent. Concomitant dissolution of olivine produces irregular-shaped relict grains preserved as cores to most kimberlitic olivine. Multiple generations of decompression cracks in olivine provide evidence for a progression in ambient fluid compositions (e.g., from carbonatitic to silicic) during ascent. Numerical modelling predicts tensile failure of xenoliths (disaggregation) and olivine (cracks) over ascent distances of 2-7 km and 15-25 km, respectively, at velocities of 0.1 to >4 m s-1. Efficient assimilation of Opx during ascent results in a silica-enriched, olivine-saturated kimberlitic melt (i.e. SiO2 >20 wt.%) that crystallizes overgrowths on partially digested and abraded olivine xenocrysts. Olivine saturation is constrained to occur at pressures <1 GPa; an

  16. Limitations on the Estimation of Parental Magma Temperature Using Olivine-melt Equilibria: Hotspots Not So Hot

    NASA Astrophysics Data System (ADS)

    Natland, J. H.

    2004-12-01

    Estimates of temperatures of magmas parental to picritic tholeiites using olivine-melt equilibria and FeO-MgO relationships depend strongly on the assumption that a liquid composition, usually a glass, is related to the most magnesian olivine in the rock, or to an olivine composition in equilibrium with mantle peridotite, along an olivine-controlled liquid line of descent. The liquid Fe2+/Fe3+ also has to be known; where data exist, average values from wet chemical determinations are used. Crystallization histories of tholeiitic picrites from islands, spreading ridges, and large igneous provinces, however, usually reveal them to be hybrid rocks that are assembled by two types of magma mixing: 1) between a) differentiated magmas that are on olivine-plagioclase or olivine-plagioclase-clinopyroxene cotectics and b) crystal sludges with abundant olivine that may have accumulated from liquids crystallizing olivine alone; and 2) between primitive magma strains in which olivine crystallized either alone or with other silicate minerals at elevated pressure on separate liquid lines of descent. Many picrites give evidence that both types of mixing have occurred. If either type has occurred, the assumption of olivine-control linking a glass and an olivine composition can only circumstantially be correct. Oxidation state can also be underestimated and therefore FeO contents overestimated if basalts have degassed S, as at Hawaii. In Case 1, hybrid host glass compositions often have higher FeO at given MgO content than liquids which produced many olivine crystals in the rock. In Case 2, the separate parental melt strains are revealed by diversity of compositions of both melt inclusions and Cr-spinel and are most often interpreted to mean local heterogeneity of the mantle source. The inclusions do not always affirm an olivine-controlled liquid line of descent. Instead, inclusions with <13% Al2O3 are increasingly interpreted from both major oxides and trace elements to be derived

  17. Phosphorus zoning in olivine of Kilauea Iki lava lake, Hawaii

    NASA Astrophysics Data System (ADS)

    Fabbrizio, Alessandro; Beckett, John R.; Baker, Michael B.; Stolper, Edward M.

    2010-05-01

    Kilauea Iki lava lake was formed when the lavas of the 1959 summit eruption of Kilauea volcano ponded in Kilauea Iki pit crater, as described by [1]. The main chamber of this lake has been drilled repeatedly from 1960 to 1981 as the lake has cooled and crystallized and partial descriptions of core can be found in [2-7]. The bulk of the core consists of a gray, olivine-phyric basalt matrix [3]. Rapid diffusion of divalent cations through olivine at magmatic temperatures can delete information on early-formed zoning and thus information on early magmatic history, recorded in olivine during its growth, is often largely lost [8-11]. In the last years many studies [8-11] have shown that natural olivine, terrestrial and extraterrestrial, from several localities and rock types can preserve a complex zoning in P (sometimes associated with Cr and Al). Simple crystallization experiments conducted by [10] and [11] were able to replicate these features (i.e., sector and oscillatory zoning). Here, we describe P, Cr and Al zoning in olivine from the 1981 drilling of Kilauea Iki lava lake hole #1 (KI81-1) [6]. Kα X-ray intensity maps and major and minor element quantitative analyses were obtained using the Caltech JEOL JXA-8200 electron microprobe. We acquired P, Cr, Al, Fe and Ti X-ray maps simultaneously at 15 kV and 400 nA, a beam diameter of 1 μm, pixel spacing of 1-2 μm, and count times of 420-1500 msec/step were used depending on the dimension of the crystal. 15 kV and 40 nA with a beam diameter of 1 μm were used to collect quantitative analyses. P2O5 contents of the Iki olivines range from below detection limit to 0.30 wt%. Zoning in phosphorus, based on X-ray intensity maps, was observed in all olivines we examined. The P zoning patterns of the olivines display several styles. P shows oscillatory zoning comparable to that seen in terrestrial and extraterrestrial igneous olivines and in experimentally grown olivine [8-11]; high P regions, inside the crystals, outline

  18. 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

  19. Impact of dissolution and carbonate precipitation on carbon storage in basalt

    NASA Astrophysics Data System (ADS)

    Wells, R. K.; Xiong, W.; Tadeoye, J.; Menefee, A.; Ellis, B. R.; Skemer, P. A.; Giammar, D.

    2016-12-01

    The spatial evolution of silicate mineral dissolution, carbonate precipitation, and the transport of fluids influence the viability of carbon storage in basalt reservoirs. Dissolution of natural basalt and subsequent carbonate precipitation in systems with different transport processes operating were characterized using static and flow-through (5 mL/hr) experiments at 50, 100, and 150 °C, and 100 bar CO2. Intact samples and cores with milled pathways that simulate fractures were tested. Spatial and mineralogical patterns in dissolution and precipitation were analyzed using optical and electron microscopy, microCT scanning, and surface roughness data. Precipitates and fluid chemistry were analyzed using Raman spectroscopy, SEM-EDS, and ICP-MS. Analysis of the bulk solution and surface topography suggests dissolution of olivine and pyroxene grains begins within hours of the start of the experiments. In flow-through experiments, total effluent cation concentrations reach a peak concentration within a few hours then drop towards a steady state within a few days. In static experiments, the initial rate of cation release is faster than it is after several weeks. In both cases Ca2+, Mg2+, and Fe2+ are the dominant cations in solution in the initial stages of reaction. Lower concentrations of Na2+, K+, and Al3+, and the preservation of feldspar and matrix grains after several weeks of reaction indicate the slow reactivity of these minerals. As the reaction progresses, the surface roughness increases steadily with cavities developing at the sites of olivine and pyroxene grains. Post-reaction analysis of basalt samples reacted at static conditions with milled pathways reveals that both siderite and amorphous silica precipitated within diffusion-limited zones as early as 4-6 weeks. Siderite abundance varies with distance along the pathway with the highest concentration of carbonates 1-2 cm below the fracture opening. Siderite precipitates are large enough to fill fracture

  20. Olivine dissolution in the presence of heterotrophic bacteria (Pseudomonas reactants) extracted from Icelandic groundwater of the CO2 injection pilot site

    NASA Astrophysics Data System (ADS)

    Shirokova, Liudmila; Pokrovsky, Oleg; Benezeth, Pascale; Gerard, Emmanuelle; Menez, Benedicte; Alfredsson, Helgi

    2010-05-01

    This work is aimed at experimental modeling of the effect of heterotrophic bacteria on dissolution of important rock-forming mineral, olivine, at the conditions of CO2 storage and sequestration. Heterotrophic aerobic gram-negative bacteria were extracted from deep underground water (HK31, 1700 m deep and, t = 25-30°C) of basaltic aquifer located within the Hellisheidi CO2 injection pilot site (Iceland). Following this sampling, we separated, using culture on nutrient agar plates, four different groups of gram-negative aerobic bacteria. The enzymatic activity of studied species has been evaluated using Biolog Ecoplates and their genetic identification was performed using 18-S RNA analysis. The optimal growth conditions of bacteria on Brain Hearth Broth nutrient have been determined as 5 to 37°C and growth media pH varied from 7.0-8.2. Culturing experiments allowed determining the optimal physico-chemical conditions for bacteria experiments in the presence of basic Ca, Mg-containing silicates. Olivine (Fo92) was chosen as typical mineral of basalt, widely considered in carbon dioxide sequestration mechanisms. Dissolution experiments were performed in constant-pH (7 to 9), bicarbonate-buffered (0.001 to 0.05 M) nutrient-diluted media in batch reactors at 0-30 bars of CO2 in the presence of various biomass of Pseudomonas reactants. The release rate of magnesium, silica and iron was measured as a function of time in the presence of live, actively growing, dead (autoclaved or glutaraldehyde-treated) cells and bacteria exometabolites. Both nutrient media diluted 10 times (to 100 mg DOC/L) and inert electrolyte (NaCl, no DOC) were used. Our preliminary results indicate that the pH and dissolved organic matter are the first-order parameters that control the element release from olivine at far from equilibrium conditions. The SEM investigation of reacted surfaces reveal formation of surface roughness with much stronger mineral alteration in the presence of live bacteria

  1. Lithium Zoning in Kīlauea Olivine: Growth vs. Diffusion?

    NASA Astrophysics Data System (ADS)

    Shea, T.; Lynn, K. J.; Garcia, M. O.; Costa Rodriguez, F.

    2016-12-01

    Lithium is a fast-diffusing element with the potential to characterize magmatic processes that occur on timescales of hours to days [1]. However, Li diffusion in olivine is complex. Experimental studies show that it can diffuse via two paths: a `fast' interstitial mechanism and a `slow' vacancy mechanism [1]. Charge balancing relationships with other incompatible trace elements may also play a role in Li diffusion [2]. A detailed study of lithium zoning in natural olivine was undertaken to better understand how Li is correlated with other trace elements and determine if Li diffusion profiles can be used to extract meaningful timescales of magmatic processes. Olivine crystals from the Keanakāko`i explosive period at Kīlauea Volcano (HI) were used in this study because (a) the lavas and tephra generally contain phenocrysts of only olivine in a rapidly quenched glass, which avoid complications of multi-phase systems and post-eruptive diffusion; (b) we previously constrained the magmatic histories of these crystals using major and minor elements; and (c) at concentrations (e.g. 1-10 ppm) and temperatures (e.g. 1150-1250 °C) typical of Kīlauea basalts, Li diffusion is probably dominated by the vacancy mechanism [1]. Euhedral crystals were carefully oriented and mounted on either the a- or b- crystallographic axes (c-axis is always within the plane of section) and polished to the crystal core. High precision LA-ICP-MS analyses of Li (2σ = 0.08 ppm), Na, Al, P, and Cr complement EPMA profiles of Si, Mg, Fe, Ni, and Ca (200 nA current). Core-to-rim transects were collected along two axes (c and a or b) to identify potential diffusion anisotropy effects for Li and other elements. Li zoning is correlated with Na, indicative of a growth signature (also observed for Al, P, and Cr), or is decoupled from incompatible trace elements and have profiles that indicate diffusive re-equilibration. Modeling of Li diffusion profiles yields timescales of hours to days, which probably

  2. Deep Crustal Structure beneath Large Igneous Provinces and the Petrologic Evolution of Flood Basalts

    NASA Astrophysics Data System (ADS)

    Richards, Mark; Ridley, Victoria

    2010-05-01

    We present a review of seismological constraints on deep crustal structures underlying large igneous provinces (LIPs), largely from wide-angle seismic refraction surveys. The main purpose of this review is to ascertain whether this seismic evidence is consistent with, or contrary to, petrological models for the genesis of flood basalt lavas. Where high-quality data are available beneath continental flood basalt (CFB) provinces (Emeishan, Columbia River, Deccan, Siberia), high-velocity structures (Vp ~6.9-7.5 km/sec) are typically found immediately overlying the Moho in layers of order ~5-15 km thick. Oceanic plateau (OP) LIPs exhibit similar layers, with a conspicuous layer of very high crustal velocity (Vp~7.7 km/sec) beneath the enormous Ontong-Java plateau. These structures are similar to inferred ultramafic underplating structures seen beneath active hotspots such as Hawaii, the Marqueses, and La Reunion. Petrogenetic models for flood basalt volcanism based on hot plume melting beneath mature lithosphere suggest that these deep seismic structures may consist in large part of cumulate bodies of olivine and clinopyroxene which result from ponding and deep-crustal fractionation of ultramafic primary melts. Such fractionation is necessary to produce basalts with typical MgO contents of ~6-8%, as observed for the vast bulk of observed flood basalts, from primary melts with MgO contents of order ~15-18% (or greater) such as result from hot, deep melting beneath the lithosphere. The volumes of cumulate bodies and ultramafic intrusions in the lowermost crust, often described in the literature as "underplating," are comparable to those of the overlying basaltic formations, also consistent with petrological models. Further definition of the deep seismic structure beneath such prominent LIPs as the Ontong-Java Plateau could place better constraints on flood basalt petrogenesis by determining the relative volumes of ultramafic bodies and basaltic lavas, thereby better

  3. Deducing Water Concentrations in the Parent Magma of Cumulate Clinopyroxene and Olivine: Implications for a Hydrous Parent Melt of a Primitive Deccan Lava

    NASA Astrophysics Data System (ADS)

    Seaman, S. J.

    2017-12-01

    Water concentrations of clinopyroxene megacrysts in the Powai ankaramite flow, located near Mumbai, Deccan province, India, indicate that the parent magma of the flow hosted at least 4.3 wt.% water, an unusually high water concentration for a continental flood basalt magma. The Powai flow hosts clinopyroxene and olivine phenocrysts. Chatterjee and Sheth (2015) showed that phenocrysts in the flow were part of a cumulate layer intruded by basaltic melt at 6 kb and 1230oC, so the phenocrysts record characteristics of the cumulate parent melt. Clinopyroxene phenocrysts are oscillatorily zoned in water, Mg, Fe, and Ca concentrations, and have concentric bands 100-200 microns thick of 10-20 micron diameter melt inclusions. Olivine phenocrysts host only larger isolated melt inclusions. Zones in the cpx phenocrysts where melt inclusion-rich concentric bands occur have higher concentrations of water than inclusion-free zones. Water concentrations of cpx were used to calculate water concentrations in the melt from which the crystals formed using partition coefficients of Hauri et al. (2004). Water concentrations in the parent magma were between 4.3 and 8.2 wt. % based on water concentrations in cpx. Both Mg and Fe are relatively depleted in the water- and melt inclusion-rich zones in cpx, and Ca is enriched in these zones. Oscillatory zoning in cpx may be a result of repeated growth of cpx in water- richer and water-poorer boundary layers where water lowered melt viscosity and enhanced diffusion and crystal growth rates. Water-enhanced growth rates may have resulted in capture of melt inclusions preserved in water-rich cpx zones. Melt inclusions in olivine phenocrysts preserve lower water concentrations ( 1.2 wt. %) than those indicated by water concentration in cpx phenocrysts. This disparity may be evidence of water loss from melt inclusions in olivine (Gaetani et al., 2009) or may indicate that cpx and ol crystals did not crystallize from the same parent at the same time.

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

    NASA Astrophysics Data System (ADS)

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

    2016-12-01

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

  5. A kinetic rate model for crystalline basalt dissolution at temperature and pressure conditions relevant for geologic CO2 sequestration

    NASA Astrophysics Data System (ADS)

    Pollyea, R.; Rimstidt, J. D.

    2016-12-01

    Geologic carbon sequestration in terrestrial basalt reservoirs is predicated on permanent CO2 trapping through CO2-water-rock dissolution reactions followed by carbonate precipitation. Bench-scale experiments have shown these reaction paths to be rapid, occurring on a timescale 100 - 102 years. Moreover, recent results from the CarbFix basalt sequestration pilot project in Iceland demonstrate >95% CO2 isolation two years after a small-scale injection. In order to assess the viability of basalt sequestration worldwide (e.g., Deccan Traps, Columbia Plateau, etc.), flexible simulation tools are required that distill the dissolution reactions into a user-friendly format that is readily transmissible to existing reactive transport numerical simulators. In the present research, we combine experimental results extant in the literature for Icelandic basalt to develop kinetic rate models describing the pH-dependent dissolution of (1) basaltic glass and (2) an aggregate mineral assemblage for crystalline basalt comprising olivine, pyroxene, and plagioclase phases. In order to utilize these kinetic rate models with numerical simulation, a thermodynamic solubility model for each phase is developed for use with the reactive transport simulation code, TOUGHREACT. We use reactive transport simulation in a simple 1-D reactor to compare dissolution of the aggregate crystalline basalt phase with the traditional formulation comprising individual mineral phases for the crystalline basalt. Simulation results are in general agreement, illustrating the efficacy of this simplified approach for modeling basalt dissolution at temperature and pressure conditions typical of geologic CO2 reservoirs. Moreover, this approach may be of value to investigators seeking dissolution models for crystalline basalt in other mafic provinces.

  6. Lithologies contributing to the clast population in Apollo 17 LKFM basaltic impact melts

    NASA Technical Reports Server (NTRS)

    Norman, Marc D.; Taylor, G. Jeffrey; Spudis, Paul; Ryder, Graham

    1992-01-01

    LKFM basaltic impact melts are abundant among Apollo lunar samples, especially those from Apollo 15, 16, and 17. They are generally basaltic in composition, but are found exclusively as impact melts. They seem to be related to basins and so could represent the composition of the lower lunar crust. They contain lithic clasts that cannot be mixed in any proportion to produce the composition of the melt matrix; components rich in transition elements (Ti, Cr, Sc) and REE are not considered. To search for the mysterious cryptic component, we previously investigated the mineral clast population in two Apollo 14 LKFM basaltic impact melts, 15445 and 15455. The cryptic component was not present in the mineral clast assemblage of these breccias either, but some olivine and pyroxene grains appeared to be from lithologies not represented among identified igneous rocks from the lunar highlands. In addition, none of the mineral clasts could be unambiguously assigned to a ferroan anorthosite source. We have now extended this study to Apollo 17, starting with two LKFM impact melt breccias (76295 and 76315) from the Apollo 17 station 6 boulder. The results from the study are presented.

  7. Minerals as mantle fingerprints: Sr-Nd-Pb-Hf in clinopyroxene and He in olivine distinguish an unusual ancient mantle lithosphere beneath the East African Rift System

    NASA Astrophysics Data System (ADS)

    Nelson, W. R.; Shirey, S. B.; Graham, D. W.

    2011-12-01

    The East African Rift System is a complex region that holds keys to understanding the fundamental geodynamics of continental break-up. In this region, the volcanic record preserves over 30 Myrs of geochemical variability associated with the interplay between shallow and deep asthenospheric sources, continental lithospheric mantle, and continental crust. One fundamental question that is still subject to debate concerns the relationship between the lithospheric mantle and the voluminous flood basalt province that erupted at ~30 Ma in Ethiopia and Yemen. Whole-rock Re-Os isotopic data demonstrate the high-Ti (HT2) flood basalts (187Os/188Ost = 0.1247-0.1329) and peridotite xenoliths (187Os/188Ost = 0.1235-0.1377) from NW Ethiopia have similar isotopic compositions. However, Sr-Nd-Pb-Hf isotopic signatures from peridotite clinopyroxene grains are different from those of the flood basalts. The peridotite clinopyroxene separates bear isotopic affinities to anciently depleted mantle (87Sr/86Sr = 0.7019-0.7029; ɛNd = 12.6-18.5; ɛHf = 13.8-27.6) - more depleted than the MORB source - rather than to the OIB-like 30 Ma flood basalts (87Sr/86Sr ~ 0.704; ɛNd = 4.7-6.7; ɛHf = 12.1-13.5). Peridotite clinopyroxenes display two groups of 206Pb/204Pb compositions: the higher 206Pb/204Pb group (18.7-19.3) is compositionally similar to the flood basalts (206Pb/204Pb = 18.97-19.02) whereas the lower 206Pb/204Pb group (17.1-17.9) overlaps with depleted mantle. This suggests that the Pb isotope systematics in some of the peridotites have been metasomatically perturbed. Helium isotopes were analyzed by crushing olivine separated from the peridotites and the flood basalts. Olivine in the peridotites has low He concentrations (0.78-4.7 ncc/g) and low 3He/4He (4.6-6.6 RA), demonstrating that they cannot be the petrogenetic precursor to the high 3He/4He (>12 RA) flood basalts. Notably, these peridotites have 3He/4He signatures consistent with a lithospheric mantle source. Therefore

  8. Sulfur solubility in hydrous Etna Basalt at temperatures from 1150 to 1250 °C and 200 MPa

    NASA Astrophysics Data System (ADS)

    Beermann, O.; Nowak, N.; Botcharnikov, R. E.; Holtz, F.

    2009-04-01

    Degassing of magmatic volatiles is strongly dependent on fluid-melt interaction at the oneset of degassing under given pressure and temperature. Most magmatic fluids are composed of hydrous multicomponental mixtures, e.g. H-O-C-S-Cl-F-Br bearing fluids. In particular the partitioning behaviour of S and Cl between basaltic melt and hydrous fluid is of interest, because the S/Cl ratio of emitted volcanic gasses correlate to the eruption style (e.g. [1], [2], [3]). In particular, this was also observed for the 2002 eruption of Mt. Etna (Sicily) [4], which is one of the worlds most active and best investigated volcanoes. Since now, there even exist no reliable data on the solubility of sulfur in hydrous silicic melts at geologic relevant temperatures for basaltic magmas (above 1050 °C), because sulfur is known to be a very aggressive component limiting the application of experimental approaches that use noble metal capsules, especially Pt and AuPd. Thus, the experiments in this study, concerning the solubility of S in natural hydrous Etna basalt at 200 MPa and temperatures from 1150 to 1250 °C at fO2 ~ NNO + 2.5 and 1200 °C at fO2 ~ NNO, were performed in olivine-AuPd double capsules, using single crystal olivine capsules (San Carlos olivine) as sample containers, which were inserted into outer Au80Pd20 capsules. The starting material was a fused and water presaturated trachybasalt from Mt. Etna (2001 eruption), containing 5 wt.% H2O. For sulfur source pyrrhotine (FeS) was used, obtaining initial S concentrations between 1-1.5 wt.% (with respect to the amount of starting material). For some experiments an olivine disc was placed between FeS and starting glass powder to avoid FeS dispersion in the melt. All experiments were conducted in internally heated argon pressure vessels (IHPV) equipped with rapid quench device. For the reduced runs an Ar-H2 mixture was load into the vessel and the H2 pressure was monitored, using the shaw membrane technique. The experimental

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

  10. Influence of fillers on the alkali activated chamotte

    NASA Astrophysics Data System (ADS)

    Dembovska, L.; Bumanis, G.; Vitola, L.; Bajare, D.

    2017-10-01

    Alkali-activated materials (AAM) exhibit remarkable high-temperature resistance which makes them perspective materials for high-temperature applications, for instance as fire protecting and insulating materials in industrial furnaces. Series of experiments were carried out to develop optimum mix proportions of AAM based on chamotte with quartz sand (Q), olivine sand (OL) and firebrick sawing residues (K26) as fillers. Aluminium scrap recycling waste was considered as a pore forming agent and 6M NaOH alkali activation solution has been used. Lightweight porous AAM have been obtained with density in range from 600 to 880 kg/m3 and compressive strength from 0.8 to 2.7 MPa. The XRD and high temperature optical microscopy was used to characterize the performance of AAM. The mechanical, physical and structural properties of the AAM were determined after the exposure to elevated temperatures at 800 and 1000°C. The results indicate that most promising results for AAM were with K26 filler where strength increase was observed while Q and OL filler reduced mechanical properties due to structure deterioration caused by expansive nature of selected filler.

  11. The Thermal Evolution of the Galapagos Mantle Plume: Insights from Al-in-Olivine Thermometry

    NASA Astrophysics Data System (ADS)

    Trela, J.; Gazel, E.; Sobolev, A. V.; Class, C.; Bizimis, M.; Jicha, B. R.; Batanova, V. G.; Denyer, P.

    2016-12-01

    The mantle plume hypothesis is widely accepted for the formation of large igneous provinces (LIP) and many ocean island basalts (OIB). Petrologic models support a mantle plume origin by indicating high mantle temperatures (>1500 °C) for some plume-melts relative to melts generated at ambient mid ocean ridge conditions (1350 °C). Mantle plumes forming LIPs and OIBs provide our primary source of information on the geochemical and lithological heterogeneity of the lower mantle. The Galapagos hotspot represents one of the most thermally and geochemically heterogeneous plumes on the planet, sustaining long-lived isotopic and lithological heterogeneity over its 90 Ma evolution. Previous petrologic studies showed that the Galapagos plume secularly cooled over time and that the decrease in the plume's temperature correlates with an increase in a recycled (pyroxenite) component. We used Al-in-olivine thermometry to show that maximum olivine crystallization temperatures confirm secular cooling of the Galapagos plume. Olivines from the early melting stages of the plume at 90 Ma (Caribbean LIP) record the highest crystallization temperatures (1600 °C). Olivines from the current archipelago record the lowest temperatures of only 1300 °C. The largest decrease in temperature occurred between 90 and 70 Ma ( 200 °C decrease) and coincides with the plume head-tail transition. Olivines from the 60-90 Ma-old accreted Galapagos-tracks in Costa Rica and Panama record higher Ni, Fe/Mn, and lower Ca contents than those from the present-day archipelago, indicating a higher abundance of pyroxenite (recycled oceanic crust) entrained in parts of the plume head that melted to form the Caribbean LIP. However, the Galapagos plume was pyroxenite-rich for 40 Ma thus pyroxenite-entrainment goes beyond the plume-tail transition. Our results suggest that hotter regions of the Galapagos plume entrained larger amounts of dense, recycled components due to their greater buoyancy; however, this

  12. Crystallization history of enriched shergottites from Fe and Mg isotope fractionation in olivine megacrysts

    NASA Astrophysics Data System (ADS)

    Collinet, Max; Charlier, Bernard; Namur, Olivier; Oeser, Martin; Médard, Etienne; Weyer, Stefan

    2017-06-01

    Martian meteorites are the only samples available from the surface of Mars. Among them, olivine-phyric shergottites are basalts containing large zoned olivine crystals with highly magnesian cores (Fo 70-85) and rims richer in Fe (Fo 45-60). The Northwest Africa 1068 meteorite is one of the most primitive "enriched" shergottites (high initial 87Sr/86Sr and low initial ε143Nd). It contains olivine crystals as magnesian as Fo 77 and is a major source of information to constrain the composition of the parental melt, the composition and depth of the mantle source, and the cooling and crystallization history of one of the younger magmatic events on Mars (∼180 Ma). In this study, Fe-Mg isotope profiles analyzed in situ by femtosecond-laser ablation MC-ICP-MS are combined with compositional profiles of major and trace elements in olivine megacrysts. The cores of olivine megacrysts are enriched in light Fe isotopes (δ56FeIRMM-14 = -0.6 to -0.9‰) and heavy Mg isotopes (δ26MgDSM-3 = 0-0.2‰) relative to megacryst rims and to the bulk martian isotopic composition (δ56Fe = 0 ± 0.05‰, δ26Mg = -0.27 ± 0.04‰). The flat forsterite profiles of megacryst cores associated with anti-correlated fractionation of Fe-Mg isotopes indicate that these elements have been rehomogenized by diffusion at high temperature. We present a 1-D model of simultaneous diffusion and crystal growth that reproduces the observed element and isotope profiles. The simulation results suggest that the cooling rate during megacryst core crystallization was slow (43 ± 21 °C/year), and consistent with pooling in a deep crustal magma chamber. The megacryst rims then crystallized 1-2 orders of magnitude faster during magma transport toward the shallower site of final emplacement. Megacryst cores had a forsterite content 3.2 ± 1.5 mol% higher than their current composition and some were in equilibrium with the whole-rock composition of NWA 1068 (Fo 80 ± 1.5). NWA 1068 composition is thus close to a

  13. Water and Carbon Dioxide Adsorption at Olivine Surfaces

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

    Kerisit, Sebastien N.; Bylaska, Eric J.; Felmy, Andrew R.

    2013-11-14

    Plane-wave density functional theory (DFT) calculations were performed to simulate water and carbon dioxide adsorption at the (010) surface of five olivine minerals, namely, forsterite (Mg2SiO4), calcio-olivine (Ca2SiO4), tephroite (Mn2SiO4), fayalite (Fe2SiO4), and Co-olivine (Co2SiO4). Adsorption energies per water molecule obtained from energy minimizations varied from -78 kJ mol-1 for fayalite to -128 kJ mol-1 for calcio-olivine at sub-monolayer coverage and became less exothermic as coverage increased. In contrast, carbon dioxide adsorption energies at sub-monolayer coverage ranged from -20 kJ mol-1 for fayalite to -59 kJ mol-1 for calcio-olivine. Therefore, the DFT calculations show a strong driving force for carbonmore » dioxide displacement by water at the surface of all olivine minerals in a competitive adsorption scenario. Additionally, adsorption energies for both water and carbon dioxide were found to be more exothermic for the alkaline-earth (AE) olivines than for the transition-metal (TM) olivines and to not correlate with the solvation enthalpies of the corresponding divalent cations. However, a correlation was obtained with the charge of the surface divalent cation indicating that the more ionic character of the AE cations in the olivine structure relative to the TM cations leads to greater interactions with adsorbed water and carbon dioxide molecules at the surface and thus more exothermic adsorption energies for the AE olivines. For calcio-olivine, which exhibits the highest divalent cation charge of the five olivines, ab initio molecular dynamics simulations showed that this effect leads both water and carbon dioxide to react with the surface and form hydroxyl groups and a carbonate-like species, respectively.« less

  14. Phenocrysts and megacrysts of olivines from ultramafic lamprophyres of the Chadobets and Il'bokich uplifts, Southwestern Siberia

    NASA Astrophysics Data System (ADS)

    Smirnova, Maria; Sazonova, Lyudmila; Nosova, Anna; Kargin, Alexey; Shcherbakov, Vasiliy

    2017-04-01

    The study of composition and zoning of olivines from ultramafic lamprophyres of the SW Siberian craton allowed us to distinguish their main types (phenocrysts and megacrysts) and to estimate the possible P-T conditions of phenocryst crystallization. The studied rocks occur as sills and dikes in the Chadobets and Il'bokich uplifts of the Irkeneeva-Chadobets trough. The ultramafic lamprophyres of these uplifts are spaced around 80 km apart and differ in age by more than 150 Ma. The rocks of the Il'bokich Uplift are dated at Devonian, while the age of the Chadobets Complex is restricted to the Triassic. The episodes of these complexes formation were separated by the large flood basalt event. According to classification (Tappe et al., 2005), the studied rocks are aillikite and damtjernite. Olivine phenocrysts from the rocks of the Il'bokich and Chadobets complexes are represented by sub- and euhedral grains. They are composed of core, transitional zone, and rim. Olivine cores in the aillikites of the Il'bokich Complex are characterized by Mg# 89; CaO - 0.13-0.14 wt %; TiO2 around 0.03 wt %, Al - 200-380 ppm, and Cr - 130-340 ppm. The cores of phenocrysts from the Chadobets lamprophyres have Mg# 85-87, CaO varying within 0.1-0.2 wt %, and TiO2 - 0.02-0.05 wt %. The megacrysts differ from the phenocrysts of these rocks in the lower Mg# 83-84 and CaO - 0.08-0.14 wt % at higher TiO2 - 0.04-0.05 wt %. Al - 100-700 ppm, Cr - 20-65 ppm. The most striking difference between olivines of the two complexes is observed between their Mg#-Ni relations. The cores of olivine phenocrysts from the Il'bokich lamprophyres are characterized by the high Mg number (Mg# = 89) and Ni content (2800-3000 ppm), whereas olivine cores of the Chadobets aillikites have higher contents of Ni (3000-3500 ppm) at lowered (Mg# = 86-88). These characteristics reflect the compositions of their protolith. The temperature was estimated using monomineral olivine thermometer based on the contents of Cr and Al

  15. Crystallization of oxidized, moderately hydrous arc basalt at mid-to-lower crustal pressures

    NASA Astrophysics Data System (ADS)

    Blatter, D. L.; Sisson, T. W.; Hankins, W. B.

    2012-12-01

    Decades of experimental work show that dry, reduced, subalkaline basalts differentiate to produce tholeiitic (high Fe/Mg) daughter liquids, however the influences of H2O and oxidation on differentiation paths are not well established. Accordingly, we performed crystallization experiments on a relatively magnesian basalt (8.7 wt% MgO) typical of mafic lavas erupted in the Cascades magmatic arc near Mount Rainier, Washington. Starting material was synthesized with 3 wt% H2O and run in 2.54 cm piston-cylinder vessels at 900, 700, and 400 MPa and 1200 to 925 degrees C. Samples were contained in Au75Pd25 capsules pre-saturated with Fe by reaction with magnetite at controlled fO2. Oxygen fugacity was controlled during high-pressure syntheses by the double capsule method using Re-ReO2 plus H2O-CO2 vapor in the outer capsule, mixed to match the expected fH2O of the vapor-undersaturated sample. Crystallization was similar at all pressures with a high temperature interval consisting of augite + olivine + orthopyroxene + Cr-spinel (in decreasing abundance). With decreasing temperature, plagioclase crystallizes, FeTi-oxides replace spinel, olivine dissolves, and finally amphibole appears. Liquids at 900 MPa track along Miyashiro's (1974) tholeiitic vs. calc-alkaline boundary, whereas those at 700 and 400 MPa become calc-alkaline by ~57 wt% SiO2 and greater. Although these evolved liquids are similar in most respects to common calc-alkaline andesites, they differ in having low-CaO due to early and abundant crystallization of augite prior to plagioclase, with the result that they become peraluminous (ASI: Al/(Na+K+Ca)>1) by ~55 wt% SiO2, similar to liquids reported in other studies of the high-pressure crystallization of hydrous basalts (Müntener and Ulmer, 2006 and references therein). A compilation of >7000 analyses of volcanic and intrusive rocks from the Cascades and the Sierra Nevada batholith shows that ASI in arc magmas increases continuously and linearly with SiO2 from

  16. The Temperature of the Icelandic Mantle Plume from Aluminium-in-Olivine Thermometry

    NASA Astrophysics Data System (ADS)

    Matthews, S.; Shorttle, O.; Maclennan, J.

    2015-12-01

    Temperature is a key control on the physical properties of the mantle, in particular the extent of melting during upwelling. It is not, however, a unique control on many of the parameters used to estimate mantle temperature. For example igneous crustal thickness which has often been used as a first-order proxy for mantle temperature, is also affected by mantle lithology and plume flux. Alternatives to geophysical indicators of mantle temperature are petrological thermometers. However, these record crystallisation temperatures, therefore a series of assumptions about the coupled melt- solid mantle thermal history must be made when calculating back to mantle potential temperature. In this study we investigate how these assumptions may affect mantle temperature estimates and how crystallisation temperatures may offer insights into the melting and melt transport processes, focussing on a new set of crystallisation temperature estimates we have made on primitive Icelandic basalts.We used the aluminium-in-olivine thermometer of Coogan et al. (2014) to estimate crystallisation temperatures of olivine phenocrysts in a suite of samples from the Northern Volcanic Zone (NVZ) of Iceland. The data suggest that within a single volcanic system crystallisation temperature depends strongly on the olivine forsterite content, thus the history of melt evolution, and how the eruption samples this, must be considered when extrapolating to mantle temperature. To assess the influence of the assumptions required to obtain mantle temperature we constructed a simple thermal model incorporating varying proportions of lherzolite, pyroxenite and harzburgite undergoing decompression melting. A trade off between increasing mantle temperature and decreasing pyroxenite (or increasing harzburgite) in the source is observed. Using this dataset and our model, calculations reveal a potential temperature of 1470±130 °C for Iceland, and a temperature excess of 150±40 °C relative to ambient mantle

  17. Electrical conductivity of basaltic and carbonatite melt-bearing peridotites at high pressures: Implications for melt distribution and melt fraction in the upper mantle

    NASA Astrophysics Data System (ADS)

    Yoshino, Takashi; Laumonier, Mickael; McIsaac, Elizabeth; Katsura, Tomoo

    2010-07-01

    Electrical impedance measurements were performed on two types of partial molten samples with basaltic and carbonatitic melts in a Kawai-type multi-anvil apparatus in order to investigate melt fraction-conductivity relationships and melt distribution of the partial molten mantle peridotite under high pressure. The silicate samples were composed of San Carlos olivine with various amounts of mid-ocean ridge basalt (MORB), and the carbonate samples were a mixture of San Carlos olivine with various amounts of carbonatite. High-pressure experiments on the silicate and carbonate systems were performed up to 1600 K at 1.5 GPa and up to at least 1650 K at 3 GPa, respectively. The sample conductivity increased with increasing melt fraction. Carbonatite-bearing samples show approximately one order of magnitude higher conductivity than basalt-bearing ones at the similar melt fraction. A linear relationship between log conductivity ( σbulk) and log melt fraction ( ϕ) can be expressed well by the Archie's law (Archie, 1942) ( σbulk/ σmelt = Cϕn) with parameters C = 0.68 and 0.97, n = 0.87 and 1.13 for silicate and carbonate systems, respectively. Comparison of the electrical conductivity data with theoretical predictions for melt distribution indicates that the model assuming that the grain boundary is completely wetted by melt is the most preferable melt geometry. The gradual change of conductivity with melt fraction suggests no permeability jump due to melt percolation at a certain melt fraction. The melt fraction of the partial molten region in the upper mantle can be estimated to be 1-3% and ˜ 0.3% for basaltic melt and carbonatite melt, respectively.

  18. Olivine and spinel fabric development in lineated peridotites

    NASA Astrophysics Data System (ADS)

    German, Lindsey; Newman, Julie; Chatzaras, Vasileios; Kruckenberg, Seth; Stewart, Eric; Tikoff, Basil

    2016-04-01

    Investigation of olivine and spinel fabrics in lineated harzburgites from the Red Hills peridotite massif, New Zealand, reveals that the spinel grain population records the same orientation of the principal finite strain axes as olivine grains, however, olivine grains generally record stronger fabric anisotropy. Further, olivine crystallographic preferred orientation (CPO) reflects the constrictional kinematic context of these rocks. In these harzburgites, deformed at ~1200 °C and >6 kbar, spinel grains are variably oriented and display weak to no CPO. Shape fabric in spinels, determined using X-ray computed tomography (XRCT) indicates a range of geometries (L>S, L=S and LOlivine grains (mean diameter: 0.13 - 0.27 mm) exhibit evidence for dislocation creep, including subgrains, undulose extinction and a strong shape preferred orientation, with long axes parallel or subparallel to the mean spinel long axis orientation derived from XRCT. Olivine fabric analyses, carried out using Image SXM on grain traces from optical photomicrographs of two mutually perpendicular thin sections from each sample, yield moderately to strongly prolate fabrics (L>S tectonites) for olivine in all samples. CPO, plotted with respect to lineation and foliation as defined by XRCT analyses of spinel grains, is characterized by [100] maxima parallel or subparallel to the lineation; [010] and [001] form girdles perpendicular to the lineation, consistent with the D-type CPO for olivine. Olivine CPO is typically interpreted in the context of deformation conditions (e.g., temperature, stress) based on experimental studies. However, the D-type CPO for olivine is generally associated with deformation at relatively lower temperatures than suggested by the mineral compositions in these rocks. Our data suggest that olivine CPO may not only respond to deformation conditions, but may be controlled by the

  19. Residual glasses and melt inclusions in basalts from DSDP Legs 45 and 46 - Evidence for magma mixing. [Deep Sea Drilling Project

    NASA Technical Reports Server (NTRS)

    Dungan, M. A.; Rhodes, J. M.

    1978-01-01

    Microprobe analyses of natural glasses in basalts recovered by Legs 45 and 46 of the Deep Sea Drilling Project are reported and interpreted in the context of other geochemical, petrographic and experimental data on the same rocks (Rhodes et al., 1978). Residual glass compositions in the moderately evolved aphyritic and abundantly phyric basalts within each site indicate that none of the units is related to any other or to a common parent by simple fractional crystallization. The compositional trends, extensive disequilibrium textures in the plagioclase phenocrysts and the presence in evolved lavas of refractory plagioclase and olivine phenocrysts bearing primitive melt inclusions provide evidence that magma mixing had a major role in the genesis of the Leg 45 and 46 basalts. The magma parental to these basalts was most likely characterized by high Mg/(Mg + Fe/+2/), CaO/Al2O3, CaO/Na2O and low lithophile concentrations. A mixing model involving incremental enrichment of magmaphile elements by repeated episodes of mixing of relatively primitive and moderately evolved magmas, followed by a small amount of fractionation is consistent with the characteristics of the basalts studied.

  20. The fate of olivine in the lower crust: Pseudomorphs after olivine in coronitic metagabbro from the Grenville Orogen, Ontario

    NASA Astrophysics Data System (ADS)

    Kendrick, J. L.; Jamieson, R. A.

    2016-09-01

    Orthopyroxene-oxide symplectites after olivine are among the most enigmatic features of corona assemblages in metagabbros. Two coronitic metagabbro bodies from the Algonquin suite in the Grenville Orogen, Ontario, contain exceptionally well preserved orthopyroxene + Fe-Ti oxide symplectite formed during prograde Ottawan (ca. 1060 Ma) granulite-facies metamorphism. Based on textural evidence, we propose a new hypothesis for the formation of these symplectites. Under oxidising conditions associated with fluid infiltration, magmatic olivine and ilmenite underwent a coupled reaction whereby magnetite produced by oxidation of olivine replaced adjacent igneous ilmenite. Ilmenite was re-precipitated as a fine-grained intergrowth with orthopyroxene and some magnetite in the former olivine sites. This hypothesis is supported by textural evidence showing partial replacement of magmatic ilmenite by magnetite and a close spatial association between magmatic oxides and orthopyroxene + Fe-Ti oxide symplectite, which locally radiates from ilmenite into olivine. Measured orthopyroxene/oxide ratios in the symplectite (20-35% oxides) agree with the ratio predicted from the proposed reaction (ca. 30%). Coronas and pseudomorphs formed during high-grade metamorphism, with increasing fO2 interpreted to result from fluid infiltration at near-peak conditions of ca. 13 kbar, 800 °C. The same samples contain red-brown fine-grained aggregates interpreted as iddingsite pseudomorphs after olivine. Raman spectroscopy suggests that the iddingsite consists largely of amorphous silica and Fe-hydroxide; textural evidence indicates that it formed by late-stage oxidation and hydration of olivine that survived earlier metamorphism. The unusual co-occurrence of granulite-facies pseudomorphs after olivine with an alteration product formed at near-surface conditions indicates that some olivine may survive protracted high-grade metamorphism in environments where fluid access is limited.

  1. 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.

  2. Chemical and isotopic diversity in basalts dredged from the East Pacific Rise at 10°S, the fossil Galapagos Rise and the Nazca plate

    USGS Publications Warehouse

    Batiza, Rodey; Oestrike, Richard; Futa, Kiyoto

    1982-01-01

    The dredges from the East Pacific Rise at about 10°S recovered unusual transitional, light rare-earth element (LREE) enriched basalts which show a range of fractionation. On the basis of their chemical and isotopic abundances, it is unlikely that the lavas are related by a single simple process of magmatic differentiation. We suggest that the mantle source region of these basalts was chemically and isotopically heterogeneous. The chemistry of LREE-depleted tholeiitic basalt dredged from near the axis of the extinct Galapagos Rise indicates complex petrogenesis and differentiation. The presence of tholeiitic basalts here indicates that unlike the Guadalupe and Mathematician fossil ridges, the Galapagos Rise has not been the site of voluminous post-abandonment alkalic volcanism. Alkalic basalts of picritic bulk composition dredged from an elongate seamount near the Galapagos Rise do not represent liquid compositions. Instead, we suggest that these alkalic liquids contain added olivine and plagioclase xenocrysts. Although most of the samples analyzed are very fresh, a few have been altered. The latter exhibit characteristic chemical and isotopic effects of seawater alteration.

  3. Nanoparticulate mineral matter from basalt dust wastes.

    PubMed

    Dalmora, Adilson C; Ramos, Claudete G; Querol, Xavier; Kautzmann, Rubens M; Oliveira, Marcos L S; Taffarel, Silvio R; Moreno, Teresa; Silva, Luis F O

    2016-02-01

    Ultra-fine and nano-particles derived from basalt dust wastes (BDW) during "stonemeal" soil fertilizer application have been the subject of some concern recently around the world for their possible adverse effects on human health and environmental pollution. Samples of BDW utilized were obtained from companies in the mining district of Nova Prata in southern Brazil for chemical characterization and nano-mineralogy investigation, using an integrated application of advanced characterization techniques such as X-ray diffraction (XRD), High Resolution-Transmission Electron microscopy (HR-TEM)/(Energy Dispersive Spectroscopy) EDS/(selected-area diffraction pattern) SAED, Field Emission-Scanning Electron Microscopy (FE-SEM)/EDS and granulometric distribution analysis. The investigation has revealed that BDW materials are dominated by SiO2, Al2O3 and Fe2O3, with a complex micromineralogy including alkali feldspar, augite, barite, labradorite, hematite, heulandrite, gypsum, kaolinite, quartz, and smectite. In addition we have identified a number of trace metals such as Cd, Cu, Cr, Zn that are preferentially concentrated into the finer, inhalable, dust fraction and could so present a health hazard in the urban areas around the basalt mining zone. The implication of this observation is that use of these nanometric-sized particulates as soil fertilizer may present different health challenges to those of conventional fertilizers, inviting future work regarding the relative toxicities of these materials. Our investigation on the particle size distribution, nano-particle mineralogy and chemical composition in typical BDW samples highlights the need to develop cleaning procedures to minimise exposure to these natural fertilizing basalt dust wastes and is thus of direct relevance to both the industrial sector of basalt mining and to agriculture in the region. Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Petrogenesis of pillow basalts from Baolai in southwestern Taiwan

    NASA Astrophysics Data System (ADS)

    Liu, Chih-Chun; Yang, Huai-Jen

    2016-04-01

    The pillow basalts from Baolai in southwestern Taiwan have been inferred to bear Dupal signautres based on their Th/Ce ratio, linking the Baolai basalts to the South China Sea (SCS) seamounts that are characterized by Dupal Pb isotope signatures (Smith and Lewis, 2007). In this study, thirty-two Baolai basalt samples were analyzed for abundances of major and trace elements as well as Pb and Nd isotope ratios to verify their Dupal characters and to constrain their petrogenesis significance. The Baolai basalts contain 4-10 % L.O.I.. Three stages of alteration are inferred from plots of L.O.I. abundance versus concentrations major oxides as well as mineral textures and compositions. The first alteration stage was characterized by albitization that converted Ca-rich plagioclase to albite. The second alteration stage was dominated by chloritization of olivine and augite, resulting in increases in L.O.I. abundance. The last alteration stage is represented by formation of secondary calcite in vesicles and cracks. These alteration processes reflect interaction with seawater and apparently did not affect the magmatic Pb isotope composition for the low Pb concentration in seawater. Relative to the North Hemisphere Reference Line (NHRL), the Baolai pillow basalts have higher 208Pb/204Pb ratios at a given 206Pb/204Pb value, showing Dupal anomaly. For their relatively higher 208Pb/204Pb, 207Pb/204Pb, and 206Pb/204Pb ratios, the Baolai basalts are distinct from majority of the Cenozoic basalts in the Hainan-Leizhou peninsula, the Indochina peninsula, and the SCS seamounts, for which derivation from the Hainan mantle plume has been recently proposed (Wang et al., 2013). In contrast, the Baolai basalts and the Cenozoic basalts from eastern Guangdong at southeastern China have similar Pb and Nd isotope compositions, indicating derivation from similar mantle sources. However, the Baolai basalts have lower abundance ratios of Zr/Hf (40.3-45.6 versus 46.5-50.5), La/Yb (12

  5. The nature of the lithosphere-asthenosphere boundary from laboratory investigations of olivine anisotropy

    NASA Astrophysics Data System (ADS)

    Hansen, Lars; Qi, Chao; Warren, Jessica; Kohlstedt, David; Holtzman, Benjamin; Wallis, David

    2017-04-01

    The nature of the lithosphere-asthenosphere boundary (LAB) determines the mechanical coupling between rigid plates and the underlying convecting mantle. Seismological studies reveal distinct reflectors (G discontinuity) in the uppermost oceanic mantle that are sometimes interpreted as the LAB. The discontinuity in seismic velocity is suggested to arise from abrupt changes in composition, including the melt fraction. Interestingly, these reflectors roughly correlate with the location of discontinuities in radial seismic anisotropy, but do not correlate with the location of discontinuities in azimuthal anisotropy. To investigate the correlation between these datasets, we draw on recent laboratory measurements of crystallographic texture development in olivine-rich rocks. The textural evolution of dry olivine aggregates has been well described in recent experiments, while micromechanical models are available for incorporating these observations into larger-scale models of upper-mantle flow. Unfortunately, the systematics of textural evolution in melt-bearing olivine aggregates have not been similarly described. Here we present a new experimental data set detailing the evolution of anisotropy during deformation of partially molten peridotite. Torsion experiments were conducted on samples composed of San Carlos olivine and basaltic melt at a temperature of 1473 K and a confining pressure of 300 MPa. Seismically fast axes of olivine tend to lie at a high angle to the flow direction in a manner similar to previous experiments. The anisotropy in these samples is weak compared to that in dry, melt-free olivine deformed to similar strains. The anisotropy also exhibits relatively little change in strength and orientation with progressive deformation. Detailed microstructural analyses allow us to distinguish between competing models for the grain-scale deformation processes, favoring one in which crystallographically controlled grain shapes govern grain rotations. We

  6. Deep crustal structure beneath large igneous provinces and the petrologic evolution of flood basalts

    NASA Astrophysics Data System (ADS)

    Ridley, Victoria A.; Richards, Mark A.

    2010-09-01

    We present a review of seismological constraints on deep crustal structures underlying large igneous provinces (LIPs), largely from wide-angle seismic refraction surveys. The main purpose of this review is to ascertain whether this seismic evidence is consistent with, or contrary to, petrological models for the genesis of flood basalt lavas. Where high-quality data are available beneath continental flood basalt (CFB) provinces (Emeishan, Columbia River, Deccan, Siberia), high-velocity structures (Vp ˜ 6.9-7.5 km/sec) are typically found immediately overlying the Moho in layers of order ˜5-15 km thick. Oceanic plateau (OP) LIPs exhibit similar layers, with a conspicuous layer of very high crustal velocity (Vp ˜ 7.7 km/sec) beneath the enormous Ontong-Java plateau. These structures are similar to inferred ultramafic underplating structures seen beneath active hot spots such as Hawaii, the Marquesas, and La Reunion. Petrogenetic models for flood basalt volcanism based on hot plume melting beneath mature lithosphere suggest that these deep seismic structures may consist in large part of cumulate bodies of olivine and clinopyroxene which result from ponding and deep-crustal fractionation of ultramafic primary melts. Such fractionation is necessary to produce basalts with typical MgO contents of ˜6-8%, as observed for the vast bulk of observed flood basalts, from primary melts with MgO contents of order ˜15-18% (or greater) such as result from hot, deep melting beneath the lithosphere. The volumes of cumulate bodies and ultramafic intrusions in the lowermost crust, often described in the literature as "underplating," are comparable to those of the overlying basaltic formations, also consistent with petrological models. Further definition of the deep seismic structure beneath such prominent LIPs as the Ontong-Java Plateau could place better constraints on flood basalt petrogenesis by determining the relative volumes of ultramafic bodies and basaltic lavas, thereby

  7. Deep Crustal Structure beneath Large Igneous Provinces and the Petrologic Evolution of Flood Basalts

    NASA Astrophysics Data System (ADS)

    Richards, M. A.; Ridley, V. A.

    2010-12-01

    We present a review of seismological constraints on deep crustal structures underlying large igneous provinces (LIPs), largely from wide-angle seismic refraction surveys. The main purpose of this review is to ascertain whether this seismic evidence is consistent with, or contrary to, petrological models for the genesis of flood basalt lavas. Where high-quality data are available beneath continental flood basalt (CFB) provinces (Emeishan, Columbia River, Deccan, Siberia), high-velocity structures (Vp ~6.9-7.5 km/sec) are typically found immediately overlying the Moho in layers of order ~5-15 km thick. Oceanic plateau (OP) LIPs exhibit similar layers, with a conspicuous layer of very high crustal velocity (Vp~7.7 km/sec) beneath the enormous Ontong-Java plateau. These structures are similar to inferred ultramafic underplating structures seen beneath active hotspots such as Hawaii, the Marquesas, and La Reunion. Petrogenetic models for flood basalt volcanism based on hot plume melting beneath mature lithosphere suggest that these deep seismic structures may consist in large part of cumulate bodies of olivine and clinopyroxene which result from ponding and deep-crustal fractionation of ultramafic primary melts. Such fractionation is necessary to produce basalts with typical MgO contents of ~6-8%, as observed for the vast bulk of observed flood basalts, from primary melts with MgO contents of order ~15-18% (or greater) such as result from hot, deep melting beneath the lithosphere. The volumes of cumulate bodies and ultramafic intrusions in the lowermost crust, often described in the literature as “underplating,” are comparable to those of the overlying basaltic formations, also consistent with petrological models. Further definition of the deep seismic structure beneath such prominent LIPs as the Ontong-Java Plateau could place better constraints on flood basalt petrogenesis by determining the relative volumes of ultramafic bodies and basaltic lavas, thereby better

  8. Mantle potential temperature estimates and primary melt compositions of the Low-Ti Emeishan flood basalt

    NASA Astrophysics Data System (ADS)

    Shellnutt, J. G.; Pham, Thuy T.

    2018-05-01

    The Late Permian Emeishan large igneous province (ELIP) is considered to be one of the best examples of a mantle plume derived large igneous province. One of the primary observations that favour a mantle plume regime is the presence of ultramafic volcanic rocks. The picrites suggest primary mantle melts erupted and that mantle potential temperatures (TP) of the ELIP were > 200oC above ambient mantle conditions. However, they may represent a mixture of liquid and cumulus olivine and pyroxene rather than primary liquids. Consequently, temperature estimates based on the picrite compositions may not be accurate. Here we calculate mantle potential temperature (TP) estimates and primary liquids compositions using PRIMELT3 for the low-Ti (Ti/Y < 500) Emeishan basalt as they represent definite liquid compositions. The calculated TP yield a range from 1400oC to 1550oC, which is consistent with variability across a mantle plume axis. The primary melt compositions of the basalts are mostly picritic. The results of this study indicate that the Emeishan basalt was produced by a high temperature regime and that a few of the ultramafic volcanic rocks may be indicative of primary liquids.

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

    NASA Technical Reports Server (NTRS)

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

    2013-01-01

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

  10. PGE in fresh basalt, hydrothermal alteration products, and volcanic incrustations of Kilauea volcano, Hawaii

    NASA Astrophysics Data System (ADS)

    Crocket, James H.

    2000-05-01

    The concentrations of Os, Ir, Pd, and Au in fresh unaltered Kilauean tholeiite were determined by radiochemical neutron activation analysis. For a suite of 18 samples, averages were: Os = 0.38 ± 0.23, Ir = 0.38 ± 0.14, Pd = 2.40 ± 1.04, and Au = 1.78 ± 0.57 (in ppb with a 1σ SD). Correlations of these metals with Co, Cr, Cu, Ni, and MgO in fresh basalts, and petrographic observations, indicate that Os and Ir are carried mainly in chromite, much of which occurs as inclusions in olivine phenocrysts. Palladium correlations suggest its occurrence partly in olivine and partly in the matrix whereas Au seems to be predominantly a matrix constituent. Altered basalts were analyzed for Ir, Pd, and Au in a suite of 19 samples from five different locations. Minor changes only in either concentrations or element ratios were found for Ir and Pd when fresh and altered rock data were compared. However, Au was consistently enriched in altered relative to fresh rocks. These results imply that Pd and Ir, in contrast to Au, will likely retain their eruptive signatures upon burial in a subaerial eruptive setting. High-temperature sulfate-dominated condensates generate incrustations enriched in Ir, Os, Au, and Pd by approximately 50, 20, 10, and 3×, respectively, relative to fresh rocks. In contrast, low-temperature native sulfur deposits are the most depleted material found in the study with Ir, Pd, and Au lower by factors of 10, 4, and 5 compared with fresh rock averages. The strong enrichments of Os and Ir in the high-temperature suite are attributed mainly to enhanced volatility in highly oxygenated magmatic hydrothermal fluids contaminated by meteoric water near the structural top of volcanic conduits. The relatively smaller Pd enrichment, which is dependent on the chloride content of fluids, implies that PGE partitioning into volcanic fume may fractionate these metals (e.g., Pd versus Ir) relative to host basalt in the eruptive process.

  11. Effect of water on the fluorine and chlorine partitioning behavior between olivine and silicate melt.

    PubMed

    Joachim, Bastian; Stechern, André; Ludwig, Thomas; Konzett, Jürgen; Pawley, Alison; Ruzié-Hamilton, Lorraine; Clay, Patricia L; Burgess, Ray; Ballentine, Christopher J

    2017-01-01

    Halogens show a range from moderate (F) to highly (Cl, Br, I) volatile and incompatible behavior, which makes them excellent tracers for volatile transport processes in the Earth's mantle. Experimentally determined fluorine and chlorine partitioning data between mantle minerals and silicate melt enable us to estimate Mid Ocean Ridge Basalt (MORB) and Ocean Island Basalt (OIB) source region concentrations for these elements. This study investigates the effect of varying small amounts of water on the fluorine and chlorine partitioning behavior at 1280 °C and 0.3 GPa between olivine and silicate melt in the Fe-free CMAS+F-Cl-Br-I-H 2 O model system. Results show that, within the uncertainty of the analyses, water has no effect on the chlorine partitioning behavior for bulk water contents ranging from 0.03 (2) wt% H 2 O (D Cl ol/melt = 1.6 ± 0.9 × 10 -4 ) to 0.33 (6) wt% H 2 O (D Cl ol/melt = 2.2 ± 1.1 × 10 -4 ). Consequently, with the effect of pressure being negligible in the uppermost mantle (Joachim et al. Chem Geol 416:65-78, 2015), temperature is the only parameter that needs to be considered for the determination of chlorine partition coefficients between olivine and melt at least in the simplified iron-free CMAS+F-Cl-Br-I-H 2 O system. In contrast, the fluorine partition coefficient increases linearly in this range and may be described at 1280 °C and 0.3 GPa with ( R 2  = 0.99): [Formula: see text]. The observed fluorine partitioning behavior supports the theory suggested by Crépisson et al. (Earth Planet Sci Lett 390:287-295, 2014) that fluorine and water are incorporated as clumped OH/F defects in the olivine structure. Results of this study further suggest that fluorine concentration estimates in OIB source regions are at least 10% lower than previously expected (Joachim et al. Chem Geol 416:65-78, 2015), implying that consideration of the effect of water on the fluorine partitioning behavior between Earth's mantle minerals and

  12. Modeling the Time-dependent Changes in Electrical Conductivity of Basaltic Melts With Redox State

    NASA Astrophysics Data System (ADS)

    Pommier, A.; Gaillard, F.; Pichavant, M.

    2008-12-01

    confirmed the increase in σ when reducing the melt. At 1200°C, for both reduction-oxidation cycles, a stable value of σ following a change in fO2 is reached in 15hours, while 2hours are needed at 1400°C. The real-time changes in σ of basaltic melts following fO2 step changes were monitored. The time-dependent changes in σ are interpreted in terms of kinetics processes due to redox reequilibration between melt and gas. The evolution of σ with time can be fitted using a diffusion-limited process for reduction in CO-CO2 gas mixtures and oxidation in air. However, a reaction at the gas-melt interface probably rate limits oxidation in CO2. Reduction and oxidation rates are similar and increase with T. Oxidation-reduction rates calculated from the analysis of the conductivity evolution with time range from 10-9 to 10-8m2/s for the T range 1200-1400°C. These reaction rates are in agreement with typical alkali diffusion coefficients in basaltic melts. However, the high value of Ea (230kJ/mol) calculated from the T dependence of the oxidation-reduction rates agrees with the Ea for alkali-Earth elements. Furthermore, microprobe analyses document the existence of alkali-Earth cation fluxes during oxidations and reductions. Such cation migration probably occurs to charge-balance electron fluxes in the melt, in agreement with the study of Cooper et al. (1996). Our results suggest that the migration of alkali and alkali-Earth elements rate-limits the redox state changes in basaltic melts, and that redox mechanisms are not restricted to oxygen chemical diffusion. A discussion of chemical vs tracer oxygen diffusion studies is proposed.

  13. Geochronology and geochemistry of basaltic rocks from the Sartuohai ophiolitic mélange, NW China: Implications for a Devonian mantle plume within the Junggar Ocean

    NASA Astrophysics Data System (ADS)

    Yang, Gaoxue; Li, Yongjun; Santosh, M.; Yang, Baokai; Yan, Jing; Zhang, Bing; Tong, Lili

    2012-10-01

    The West Junggar domain in NW China is a distinct tectonic unit of the Central Asian Orogenic Belt (CAOB). It is composed of Paleozoic ophiolitic mélanges, arcs and accretionary complexes. The Sartuohai ophiolitic mélange in the eastern West Junggar forms the northeastern part of the Darbut ophiolitic mélange, which contains serpentinized harzburgite, pyroxenite, dunite, cumulate, pillow lava, abyssal radiolarian chert and podiform chromite, overlain by the Early Carboniferous volcano-sedimentary rocks. In this paper we report new geochronological and geochemical data from basaltic and gabbroic blocks embedded within the Sartuohai ophiolitic mélange, to assess the possible presence of a Devonian mantle plume in the West Junggar, and evaluate the petrogenesis and implications for understanding of the Paleozoic continental accretion of CAOB. Zircon U-Pb analyses from the alkali basalt and gabbro by laser ablation inductively coupled plasma mass spectrometry yielded weighted mean ages of 375 ± 2 Ma and 368 ± 11 Ma. Geochemically, the Sartuohai ophiolitic mélange includes at least two distinct magmatic units: (1) a Late Devonian fragmented ophiolite, which were produced by ca. 2-10% spinel lherzolite partial melting in arc-related setting, and (2) contemporary alkali lavas, which were derived from 5% to 10% garnet + minor spinel lherzolite partial melting in an oceanic plateau or a seamount. Based on detailed zircon U-Pb dating and geochemical data for basalts and gabbros from the Sartuohai ophiolitic mélange, in combination with previous work, indicate a complex evolution by subduction-accretion processes from the Devonian to the Carboniferous. Furthermore, the alkali basalts from the Sartuohai ophiolitic mélange might be correlated to a Devonian mantle plume-related magmatism within the Junggar Ocean. If the plume model as proposed here is correct, it would suggest that mantle plume activity significantly contributed to the crustal growth in the CAOB.

  14. Experimental Reproduction of Olivine rich Type-I Chondrules

    NASA Technical Reports Server (NTRS)

    Smith, Robert K.

    2005-01-01

    Ordinary chondritic meteorites are an abundant type of stony meteorite characterized by the presence of chondrules. Chondrules are small spheres consisting of silicate, metal, and sulfide minerals that experienced melting in the nebula before incorporation into chondritic meteorite parent bodies. Therefore, chondrules record a variety of processes that occurred in the early solar nebula. Two common types of unequilibrated chondrules with porphyritic textures include FeO-poor (type I) and FeO-rich (type II) each subdivided into an A (SiO2-poor) and B (SiO2-rich) series. Type IA chondrules include those with high proportions of olivine phenocrysts (>80% olivine) and type IB chondrules include those with high proportions of pyroxene phenocrysts (<20% olivine). An intermediate composition, type IAB chondrules include those chondrules in which the proportion of olivine phenocrysts is between 20-80%. We conducted high-temperature laboratory experiments (melting at 1550 C) to produce type I chondrules from average unequilibrated ordinary chondrite (UOC) material mixed with small amounts of additional olivine. The experiments were conducted by adding forsteritic rich olivine (San Carlos olivine, Fo 91) to UOC material (GRO 95544) in a 30/70 ratio, respectively. Results of these high temperature experiments suggest that we have replicated type IA chondrule textures and compositions with dynamic crystallization experiments in which a heterogeneous mixture of UOC (GRO 95544) and olivine (San Carlos olivine) were melted at 1550 C for 1 hr. and cooled at 5-1000 C/hr using graphite crucibles in evacuated silica tubes to provide a reducing environment.

  15. 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.

  16. Collision-induced basalt eruptions at Pleiku and Buôn Mê Thuột, south-central Viet Nam

    NASA Astrophysics Data System (ADS)

    Hoàng, Nguyễn; Flower, Martin F. J.; Chí, Cung Thu'ọ'ng; Xuân, Phạm Tích; Quý, Hoàng Văn; Sơn, Trần Thanh

    2013-09-01

    Neogene-Quaternary basalts occur as dispersed volcanic clusters in the vicinity of the Tethyan tectonic belt, possibly representing 'far-field' effects of the Early Tertiary collisions of Gondwana fragments with the southern margin of Eurasia. In Indochina, such a 'Diffuse Igneous Province' post-dates the 45-42 Ma 'hard' India-Asia collision and southeastward, collision induced (c. 30-17 Ma.), extrusion of Indochina. Extrusion was accommodated by left-lateral strike-slip shearing on the Ailao Shan-Red River Fault, coeval with seafloor spreading in the East Viet Nam (South China) Sea. The Indochina basalts mostly comprise shield-building tholeiites capped by small-volume undersaturated types, the latter often bearing mantle xenoliths and 'exotic' xenocrysts such as sapphire, zircon. They appeared at c. 17 Ma, more-or-less coinciding with the cessation of both continental extrusion and seafloor spreading. At this point extensional stress appears to have shifted westwards to continental Indochina, with magmatic activity appearing, characteristically, at 'pull-apart' basins. However, the relationship of mantle melting beneath this region to its geodynamic setting is controversial, being variously attributed to mantle plumes, extreme lithospheric stretching, and lateral asthenospheric displacement. There is little or no definitive evidence for regional mantle upwelling while lithosphere stretching alone appears to be insufficient to allow for melting, Here, we present geochemical and Sr, Nd, and Pb isotopic (and paleomagnetic data), for cored sections from the Pleiku and Buon Mê Thuột plateaus in south-central Viet Nam, representative in most respects of the Indochina province as a whole. In the Pleiku shield olivine tholeiite flows are intercalated with quartz tholeiites while, in contrast, alkali basalts predominate over olivine tholeiite in the Buon Mê Thuột (BMT) shield. The first of these features (in Pleiku) probably reflects crustal wall-rock reaction while

  17. Surface chemistry associated with the cooling and subaerial weathering of recent basalt flows

    USGS Publications Warehouse

    White, A.F.; Hochella, M.F.

    1992-01-01

    The surface chemistry of fresh and weathered historical basalt flows was characterized using surface-sensitive X-ray photoelectron spectroscopy (XPS). Surfaces of unweathered 1987-1990 flows from the Kilauea Volcano, Hawaii, exhibited variable enrichment in Al, Mg, Ca, and F due to the formation of refractory fluoride compounds and pronounced depletion in Si and Fe from the volatilization of SiF4 and FeF3 during cooling. These reactions, as predicted from shifts in thermodynamic equilibrium with temperature, are induced by diffusion of HF from the flow interiors to the cooling surface. The lack of Si loss and solid fluoride formation for recent basalts from the Krafla Volcano, Iceland, suggest HF degassing at higher temperatures. Subsequent short-term subaerial weathering reactions are strongly influenced by the initial surface composition of the flow and therefore its cooling history. Successive samples collected from the 1987 Kilauea flow demonstrated that the fluoridated flow surfaces leached to a predominantly SiO2 composition by natural weathering within one year. These chemically depleted surfaces were also observed on Hawaiian basalt flows dating back to 1801 AD. Solubility and kinetic models, based on thermodynamic and kinetic data for crystalline AlF3, MgF2, and CaF2, support observed elemental depletion rates due to chemical weathering. Additional loss of alkalis from the Hawaiian basalt occurs from incongruent dissolution of the basalt glass substrate during weathering. ?? 1992.

  18. An Amoeboid Olivine Aggregate in LEW 85300

    NASA Technical Reports Server (NTRS)

    Komatsu, M. D.; Yamaguchi, A.; Fagan, T. J.; Zolensky, M. E.; Shiran, N.; Mikouchi, T.

    2016-01-01

    Amoeboid Olivine aggregates (AOAs) are irregularly shaped objects commonly observed in carbonaceous chondrites. Because they are composed of fine-grained olivine and Ca-Al-rich minerals, they are sensitive indicators for nebular process and parent body alteration of their parent bodies. Recently an AOA was found in a carbonaceous clast in polymict eucrite LEW 85300. The bulk major element composition of the clast matrix in LEW 85300 suggests a relation to CM, CO and CV chondrites, whereas bulk clast trace and major element compositions do not match any carbonaceous chondrite, suggesting they have a unique origin. Here we characterize the mineralogy of AOA in LEW 85300 and discuss the origin of the carbonaceous clasts. Results and Discussion: The AOA is located in an impact melt vein. Half of the aggregate shows recrystallization textures (euhedral pyroxene and molten metal/FeS) due to impact melting, but the remaining part preserves the original texture. The AOA is composed of olivine, FeS and Mg,Al-phyllosilicate. Individual olivine grains measure 1-8 microns, with Fe-rich rims, probably due to impact heating. Olivines in the AOA are highly forsteritic (Fo95-99), indicating that the AOA escaped thermal metamorphism [4]. Although no LIME (Low-Fe, Mn-Enriched) olivine is observed, forsterite composition and the coexistence of Mg,Al-phyllosilicate suggest that the AOA is similar to those in the Bali-type oxidized CV (CVoxB) and CR chondrites. However, it should be noted that fayalitic olivine, which commonly occurs in CVoxB AOA, is not observed in this AOA. Also, the smaller grain size (<8 microns) of olivine suggests they may be related to CM or CO chondrites. Therefore, we cannot exclude the possibility that the AOA originated from a unique carbonaceous chondrite.

  19. Weathering of Basaltic Rocks from the Gusev Plains up into the Columbia Hills from the Perspective of the MER Mossbauer Spectrometer

    NASA Technical Reports Server (NTRS)

    Schroeder, C.; Klingelhoefer, G.; Morris, R. V.; Rodionov, D. S.; deSouza, P. A.; Ming, D. W.; Yen, A. S.; Gellert, R.; Bell, J. F., III

    2005-01-01

    Rocks on the ejecta blanket of Bonneville crater and along Spirit s traverse over the Gusev plains towards the Columbia Hills are angular and strewn across the surface. They have a basaltic composition [1,2], and their Mossbauer spectra are dominated by an olivine doublet [1]. The ubiquitous presence of abundant olivine in rocks and in surrounding soil suggests that physical rather than chemical weathering processes currently dominate the plains at Gusev crater [1]. However, MB spectra of rocks and outcrops in the Columbia Hills suggest more aggressive alteration processes have occurred. Ascending into the hills, Spirit encountered outcrop and rocks exhibiting layered structures. Some scattered rocks at the foot of the Columbia Hills appeared "rotten" or highly altered by physical and/or chemical processes (fig. 1). Mossbauer spectra of those rocks show a decrease in olivine accompanied by an increase in the Fe-oxides magnetite, hematite, and nanophase Fe3+ -oxides (fig. 2), suggesting that chemical weathering processes in the presence of water have altered these rocks and outcrops.

  20. Naming Lunar Mare Basalts: Quo Vadimus Redux

    NASA Astrophysics Data System (ADS)

    Ryder, G.

    1999-01-01

    Nearly a decade ago, I noted that the nomenclature of lunar mare basalts was inconsistent, complicated, and arcane. I suggested that this reflected both the limitations of our understanding of the basalts, and the piecemeal progression made in lunar science by the nature of the Apollo missions. Although the word "classification" is commonly attached to various schemes of mare basalt nomenclature, there is still no classification of mare basalts that has any fundamental grounding. We remain basically at a classification of the first kind in the terms of Shand; that is, things have names. Quoting John Stuart Mill, Shand discussed classification of the second kind: "The ends of scientific classification are best answered when the objects are formed into groups respecting which a greater number of propositions can be made, and those propositions more important than could be made respecting any other groups into which the same things could be distributed." Here I repeat some of the main contents of my discussion from a decade ago, and add a further discussion based on events of the last decade. A necessary first step of sample studies that aims to understand lunar mare basalt processes is to associate samples with one another as members of the same igneous event, such as a single eruption lava flow, or differentiation event. This has been fairly successful, and discrete suites have been identified at all mare sites, members that are eruptively related to each other but not to members of other suites. These eruptive members have been given site-specific labels, e.g., Luna24 VLT, Apollo 11 hi-K, A12 olivine basalts, and Apollo 15 Green Glass C. This is classification of the first kind, but is not a useful classification of any other kind. At a minimum, a classification is inclusive (all objects have a place) and exclusive (all objects have only one place). The answer to "How should rocks be classified?" is far from trivial, for it demands a fundamental choice about nature

  1. The timing of alkali metasomatism in paleosols

    NASA Technical Reports Server (NTRS)

    MacFarlane, A. W.; Holland, H. D.

    1991-01-01

    We have measured the concentrations of rubidium and strontium and 87Sr/86Sr values of whole-rock samples from three paleosols of different ages. The oldest of the three weathering horizons, the 2,760 Ma Mt. Roe #1 paleosol in the Fortescue Group of Western Australia, experienced addition of Rb, and probably Sr, at 2,168 +/- 10 Ma. The intermediate paleosol, developed on the Hekpoort Basalt in South Africa, is estimated to have formed at 2,200 Ma, and yields a Rb-Sr isochron age of 1,925 +/- 32 Ma. The youngest of the three paleosols, developed on the Ongeluk basalt in Griqualand West, South Africa ca. 1,900 Ma, yielded a Rb-Sr age of 1,257 +/- 11 Ma. The Rb-Sr systematics of all three paleosols were reset during post-weathering metasomatism related to local or regional thermal disturbances. The Rb-Sr systematics of the paleosols were not subsequently disturbed. The near-complete removal of the alkali and alkaline earth elements from these paleosols during weathering made them particularly susceptible to resetting of their Rb-Sr systematics. Paleosols of this type are therefore sensitive indicators of the timing of thermal disturbances.

  2. Transition Element Abundances in MORB Basalts

    NASA Astrophysics Data System (ADS)

    Yang, S.; Humayun, M.; Salters, V. J.; Fields, D.; Jefferson, G.; Perfit, M. R.

    2012-12-01

    The mineralogy of the mantle sources of basalts is an important, but hard to constrain parameter, especially with the basalts as chemical probes of major element mantle composition. Geophysical models imply that the deep mantle may have significant variations in Fe and Si relative to the ambient mantle sampled by MORB. Some petrological models of sub-ridge melting involve both pyroxenite and peridotite, implying that basalts preferentially sample a pyroxenite endmember. The First-Row Transition Elements (FRTE), Ga and Ge are compatible to moderately incompatible during partial melting, and are sensitive to mineralogical variability in the mantle and thus can provide constraints on mantle source mineralogy for MORB. We have analyzed major elements, FRTE, Ga and Ge on 231 basaltic glasses from the Middle Atlantic Ridge (MAR between -23°S to 36.44°N), 30 Mid-Cayman Rise basaltic glasses, 12 glasses from the Siqueiros Fracture Zone (EPR), 9 glasses from the Blanco Trough, Juan de Fuca ridge, and Galapagos Spreading Centers (EPR), and 4 Indian Ocean MORB. Large spots (150 μm) were precisely (±1%) analyzed by a New Wave UP193FX excimer (193 nm) laser ablation system coupled to a high-resolution ICP-MS at the National High Magnetic Field Laboratory using a high ablation rate (50 Hz) to yield blank contributions <1% for all elements, particularly Ge. The data demonstrate that the Ge/Si (6.96 x 10E-6 ± 3%, 1σ) and Fe/Mn (55 ± 2%) ratios for MORB are insensitive to fractional crystallization within the MgO range 6%-10%. MORB have Zn/Fe (9.9 x 10E-4 ± 7%), Ga/Sc (0.37-0.50), Ga/Al (2.2 x 10E-4 ± 11%) ratios, with the variations mostly due to the effects of fractional crystallization. Recent experimental determination of FRTE, Ga and Ge partition coefficients provide a framework within which to interpret these data [1]. Using these new partition coefficients, we have modeled the sensitivity of each element to mineralogical variations in the mantle source. Olivine

  3. The Mantle and Basalt-Crust Interaction Below the Mount Taylor Volcanic Field, New Mexico

    NASA Technical Reports Server (NTRS)

    Schrader, Christian M.; Crumpler, Larry S.; Schmidt, Marick E.

    2010-01-01

    The Mount Taylor Volcanic Field (MTVF) lies on the Jemez Lineament on the southeastern margin of the Colorado Plateau. The field is centered on the Mt. Taylor composite volcano and includes Mesa Chivato to the NE and Grants Ridge to the WSW. MTVF magmatism spans approximately 3.8-1.5 Ma (K-Ar). Magmas are dominantly alkaline with mafic compositions ranging from basanite to hy-basalt and felsic compositions ranging from ne-trachyte to rhyolite. We are investigating the state of the mantle and the spatial and temporal variation in basalt-crustal interaction below the MTVF by examining mantle xenoliths and basalts in the context of new mapping and future Ar-Ar dating. The earliest dated magmatism in the field is a basanite flow south of Mt. Taylor. Mantle xenolith-bearing alkali basalts and basanites occur on Mesa Chivato and in the region of Mt. Taylor, though most basalts are peripheral to the main cone. Xenolith-bearing magmatism persists at least into the early stages of conebuilding. Preliminary examination of the mantle xenolith suite suggests it is dominantly lherzolitic but contains likely examples of both melt-depleted (harzburgitic) and melt-enriched (clinopyroxenitic) mantle. There are aphyric and crystal-poor hawaiites, some of which are hy-normative, on and near Mt. Taylor, but many of the more evolved MTVF basalts show evidence of complex histories. Mt. Taylor basalts higher in the cone-building sequence contain >40% zoned plagioclase pheno- and megacrysts. Other basalts peripheral to Mt. Taylor and at Grants Ridge contain clinopyroxene and plagioclase megacrysts and cumulate-textured xenoliths, suggesting they interacted with lower crustal cumulates. Among the questions we are addressing: What was the chemical and thermal state of the mantle recorded by the basaltic suites and xenoliths and how did it change with time? Are multiple parental basalts (Si-saturated vs. undersaturated) represented and, if so, what changes in the mantle or in the tectonic

  4. Red Sea rift-related Quseir basalts, central Eastern Desert, Egypt: Petrogenesis and tectonic processes

    NASA Astrophysics Data System (ADS)

    Farahat, Esam S.; Ali, Shehata; Hauzenberger, Christoph

    2017-01-01

    Mineral and whole-rock chemistry of Red Sea rift-related Tertiary basalts from south Quseir city, central Eastern Desert of Egypt is presented to investigate their petrogenesis and relationship to tectonic processes. The south Quseir basalts (SQB) are classified as high-Ti (TiO2 >2 wt.%) subalkaline transitional lava emplaced in an anorogenic tectonic setting. Their Mg# varies from 48 to 53 indicating the evolved nature of the SQB. Pearce element ratios suggest that the SQB magmas evolved via fractional crystallization of olivine + clinopyroxene ± plagioclase, but the absence of Eu anomalies argues against significant plagioclase fractionation. Clinopyroxene compositions provide evidence for polybaric fractionation of the parental mafic magmas. Estimated temperatures of crystallization are 1015 to 1207 °C for clinopyroxene and 1076 to 1155 °C for plagioclase. These values are interpreted to result from early stage crystallization of clinopyroxene followed by concurrent crystallization of clinopyroxene and plagioclase. The incompatible trace element signatures of the SQB (La/Ba = 0.08-0.10 and La/Nb = 0.89-1.04) are comparable to those of ocean island basalts (OIB) generated from an asthenospheric mantle source unaffected by subduction components. Modeling calculations indicate that the SQB primary magmas were derived from 4-5% partial melting of a garnet-bearing lherzolite mantle source. The NE Egyptian basaltic volcanism is spatially and temporally related to Red Sea rifting and to the local E-W striking faults, confirming a relationship to tectonic activity. Our results suggest that the extensional regime associated with Red Sea rifting controlled the generation of the Egyptian basalts, likely as a result of passive upwelling of asthenospheric mantle.

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

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

    Strong mixing trends on a (Th-230/Th-232) versus Th diagram show that the basalts are mixed magmas which have undergone interaction with the crust. Instantaneous Th/U ratios are less than time integrated ones but these exceed the Th/U ratios in the MORB and OIB sources. This indicates that the mantle may have undergone some metasomatic fluxing, crustal contamination of the basalts will also enhance these ratios. Early activity on the Akira plain is represented by early basalts and hawaiites. The early basalt samples are known to predate the earliest comendites. The most recent phase of activity is represented by another cinder cone 40-50 m high being feldspar and clinopyroxene phyric. Inclusions which occur in the comendites vary in size and distribution. The largest and most porphyritic are the trachytes (up to 40 cm) with alkali feldspar phases up to 6 mm and small pyroxenes in the ground mass. The second set of inclusions are smaller (up to 10 cm) and are largely aphyric. The distribution of the inclusions are not uniform, the Broad Acres (C5) lavas contain 2-5 percent. The size of the inclusions decrease from south to north, as does the abundance of the trachytic inclusions. The major element variations in the Naivasha basalts, hawaiites and magmatic inclusions are discussed.

  6. Texture and Elastic Anisotropy of Mantle Olivine

    NASA Astrophysics Data System (ADS)

    Nikitin, A. N.; Ivankina, T. I.; Bourilitchev, D. E.; Klima, K.; Locajicek, T.; Pros, Z.

    Eight olivine rock samples from different European regions were collected for neu- tron texture analyses and for P-wave velocity measurements by means of ultrasonic sounding at various confining pressures. The orientation distribution functions (ODFs) of olivine were determined and pole figures of the main crystallographic planes were calculated. The spatial P-wave velocity distributions were determined at confining pressures from 0.1 to 400 MPa and modelled from the olivine textures. In dependence upon the type of rock (xenolith or dunite) different behavior of both the P-wave veloc- ity distributions and the anisotropy coefficients with various confining pressures was observed. In order to explain the interdependence of elastic anisotropy and hydrostatic pressure, a model for polycrystalline olivine rocks was suggested, which considers the influence of the crystallographic and the mechanical textures on the elastic behaviour of the polycrystal. Since the olivine texture depends upon the active slip systems and the deformation temperature, neutron texture analyses enable us to estimate depth and thermodynamical conditions during texture formation.

  7. Non-Newtonian behavior of plagioclase-bearing basaltic magma: Subliquidus viscosity measurement of the 1707 basalt of Fuji volcano, Japan

    NASA Astrophysics Data System (ADS)

    Ishibashi, Hidemi

    2009-03-01

    Laboratory measurements of viscosity were done for basalt erupted in 1707 AD from Fuji volcano, Japan, using a concentric cylinder rotational viscometer at temperatures of 1297-1157 °C, 1 atm pressure, and fO 2 near the Ni-NiO buffer. On cooling, elongated plagioclase crystals with a mean length/width ratio of ca. 8.5 appeared at 1237 °C, followed by olivine at 1157 °C. At progressively lower temperatures, the total crystal volume fraction increased monotonously to ca. 0.25; viscosity increased from 38.9 to 765 Pa s at a shear strain rate of 1 s - 1 . This basalt magma behaves as a Newtonian fluid at temperatures greater than 1217 °C, but shear-thinning behavior occurs at temperatures less than 1197 °C because of the suspended plagioclase crystals. This behavior is well approximated as a power law fluid. At the onset of shear thinning, the crystal volume fraction was between 0.06 and 0.13, which is attributed to the pronounced lath-shape of plagioclase crystals. The relative viscosity increases monotonously with increase of crystal volume fraction at a constant shear strain rate, and with decrease of shear strain rate at a constant crystal volume fraction. A modified form of the Krieger-Dougherty equation is introduced herein. It enables us to describe the dependencies of relative viscosity on both the crystal volume fraction and shear strain rate, and consequently the onset of shear-thinning behavior.

  8. Change in Frictional Behavior during Olivine Serpentinization

    NASA Astrophysics Data System (ADS)

    Xing, T.; Zhu, W.; French, M. E.; Belzer, B.

    2017-12-01

    Hydration of mantle peridotites (serpentinization) is pervasive at plate boundaries. It is widely accepted that serpentinization is intrinsically linked to hydromechanical processes within the sub-seafloor, where the interplay between cracking, fluid supply and chemical reactions is responsible for a spectrum of fault slip, from earthquake swarms at the transform faults, to slow slip events at the subduction zone. Previous studies demonstrate that serpentine minerals can either promote slip or creep depend on many factors that include sliding velocity, temperature, pressure, interstitial fluids, etc. One missing link from the experimental investigation of serpentine to observations of tectonic faults is the extent of alteration necessary for changing the frictional behaviors. We quantify changes in frictional behavior due to serpentinization by conducting experiments after in-situ serpentinization of olivine gouge. In the sample configuration a layer of powder is sandwiched between porous sandstone blocks with 35° saw-cut surface. The starting material of fine-grained (63 120 µm) olivine powder is reacted with deionized water for 72 hours at 150°C before loading starts. Under the conventional triaxial configuration, the sample is stressed until sliding occurs within the gouge. A series of velocity-steps is then performed to measure the response of friction coefficient to variations of sliding velocity from which the rate-and-state parameters are deduced. For comparison, we measured the frictional behavior of unaltered olivine and pure serpentine gouges.Our results confirm that serpentinization causes reduced frictional strength and velocity weakening. In unaltered olivine gouge, an increase in frictional resistance with increasing sliding velocity is observed, whereas the serpentinized olivine and serpentine gouges favor velocity weakening behaviors at the same conditions. Furthermore, we observed that high pore pressures cause velocity weakening in olivine but

  9. Crystallization of oxidized, moderately hydrous arc basalt at mid- to lower-crustal pressures: implications for andesite genesis

    NASA Astrophysics Data System (ADS)

    Blatter, Dawnika L.; Sisson, Thomas W.; Hankins, W. Ben

    2013-09-01

    This study focuses on the production of convergent margin calc-alkaline andesites by crystallization-differentiation of basaltic magmas in the lower to middle crust. Previous experimental studies show that dry, reduced, subalkaline basalts differentiate to tholeiitic (high Fe/Mg) daughter liquids, but the influences of H2O and oxidation on differentiation are less well established. Accordingly, we performed crystallization experiments at controlled oxidized fO2 (Re-ReO2 ≈ ΔNi-NiO + 2) on a relatively magnesian basalt (8.7 wt% MgO) typical of mafic magmas erupted in the Cascades near Mount Rainier, Washington. The basalt was synthesized with 2 wt% H2O and run at 900, 700, and 400 MPa and 1,200 to 950 °C. A broadly clinopyroxenitic crystallization interval dominates near the liquidus at 900 and 700 MPa, consisting of augite + olivine + orthopyroxene + Cr-spinel (in decreasing abundance). With decreasing temperature, plagioclase crystallizes, Fe-Ti-oxide replaces spinel, olivine dissolves, and finally amphibole appears, producing gabbroic and then amphibole gabbroic crystallization stages. Enhanced plagioclase stability at lower pressure narrows the clinopyroxenitic interval and brings the gabbroic interval toward the liquidus. Liquids at 900 MPa track along Miyashiro's (Am J Sci 274(4):321-355, 1974) tholeiitic versus calc-alkaline boundary, whereas those at 700 and 400 MPa become calc-alkaline at silica contents ≥56 wt%. This difference is chiefly due to higher temperature appearance of magnetite (versus spinel) at lower pressures. Although the evolved liquids are similar in many respects to common calc-alkaline andesites, the 900 and 700 MPa liquids differ in having low CaO concentrations due to early and abundant crystallization of augite, with the result that those liquids become peraluminous (ASI: molar Al/(Na + K + 2Ca) > 1) at ≥61 wt% SiO2, similar to liquids reported in other studies of the high-pressure crystallization of hydrous basalts (M

  10. Crystallization of oxidized, moderately hydrous arc basalt at mid- to lower-crustal pressures: Implications for andesite genesis

    USGS Publications Warehouse

    Blatter, Dawnika L.; Sisson, Thomas W.; Hankins, W. Ben

    2013-01-01

    This study focuses on the production of convergent margin calc-alkaline andesites by crystallization–differentiation of basaltic magmas in the lower to middle crust. Previous experimental studies show that dry, reduced, subalkaline basalts differentiate to tholeiitic (high Fe/Mg) daughter liquids, but the influences of H2O and oxidation on differentiation are less well established. Accordingly, we performed crystallization experiments at controlled oxidized fO2 (Re–ReO2 ≈ ΔNi–NiO + 2) on a relatively magnesian basalt (8.7 wt% MgO) typical of mafic magmas erupted in the Cascades near Mount Rainier, Washington. The basalt was synthesized with 2 wt% H2O and run at 900, 700, and 400 MPa and 1,200 to 950 °C. A broadly clinopyroxenitic crystallization interval dominates near the liquidus at 900 and 700 MPa, consisting of augite + olivine + orthopyroxene + Cr-spinel (in decreasing abundance). With decreasing temperature, plagioclase crystallizes, Fe–Ti-oxide replaces spinel, olivine dissolves, and finally amphibole appears, producing gabbroic and then amphibole gabbroic crystallization stages. Enhanced plagioclase stability at lower pressure narrows the clinopyroxenitic interval and brings the gabbroic interval toward the liquidus. Liquids at 900 MPa track along Miyashiro’s (Am J Sci 274(4):321–355, 1974) tholeiitic versus calc-alkaline boundary, whereas those at 700 and 400 MPa become calc-alkaline at silica contents ≥56 wt%. This difference is chiefly due to higher temperature appearance of magnetite (versus spinel) at lower pressures. Although the evolved liquids are similar in many respects to common calc-alkaline andesites, the 900 and 700 MPa liquids differ in having low CaO concentrations due to early and abundant crystallization of augite, with the result that those liquids become peraluminous (ASI: molar Al/(Na + K + 2Ca) > 1) at ≥61 wt% SiO2, similar to liquids reported in other studies of the high-pressure crystallization of hydrous basalts

  11. Origin of olivine at Copernicus

    NASA Technical Reports Server (NTRS)

    Pieters, C. M.; Wilhelms, D. E.

    1985-01-01

    The central peaks of Copernicus are among the few lunar areas where near-infrared telescopic reflectance spectra indicate extensive exposures of olivine. Other parts of Copernicus crater and ejecta, which were derived from highland units in the upper parts of the target site, contain only low-Ca pyroxene as a mafic mineral. The exposure of compositionally distinct layers including the presence of extensive olivine may result from penetration to an anomalously deep layer of the crust or to the lunar mantle. It is suggested that the Procellarum basin and the younger, superposed Insularum basin have provided access to these normally deep-seated crustal or mantle materials by thinning the upper crustal material early in lunar history. The occurrences of olivine in portions of the compositionally heterogeneous Aristarchus Region, in a related geologic setting, may be due to the same sequence of early events.

  12. Experimental Replication of Relict "Dusty" Olivine in Type 1B Chondrules

    NASA Technical Reports Server (NTRS)

    Lofgren, Gary E.; Le, L.

    2002-01-01

    Introduction: Relict "dusty" olivine is considered to be a remnants of previous chondrule forming events based on petrographic and chemical evidence. Dynamic crystallization experiments confirm that dusty olivine can be produced by reduction of FeO-rich olivine in Unequilibrated Ordinary Chondrite (UOC) material. The results of these experiments compliment those of who also produced dusty olivine, but from synthetic starting materials. Techniques: Dynamic crystallization experiments were conducted in which UOC material was reduced in presence of graphite. Starting material was coarsely ground GR095554 or WSG95300 that contained olivine of Fo 65-98. Approximately 75 mg. of UOC material was placed in a graphite crucible and sealed in an evacuated silica tube. The tube was suspended in a gas-mixing furnace operated at 1 log unit below the IW buffer. The experiments were as brief as 1.5 hrs up to 121 hrs. Results: Dusty olivine was produced readily in experiments melted at 1400 C for I hr. and cooled between 5 and 100 C/hr or melted at 1300-1400 C for 24 hours. Fe-rich olivine (dusty olivine precursors) that have been partially reduced were common in the experiments melted at 1400 C and cooled at 1000 C/hr or melted at 1200 C for 24 hrs. Relict olivine is absent in experiments melted at 1400 for 24 hrs, melted above 1400 C, or cooled more slowly than 10 C/hr. Relict olivine in the experiments has minimum Fo value of 83 . Thus even in the shortest experiments the most Fe-rich olivine has been altered significantly. The precursor olivine disappears in a few to many hours depending on temperature. The experiments show Fe-rich olivine in all stages of transition to the new dusty form. The olivine is reduced to form dusty olivine in a matter of a few hours at temperatures less than 1400 C and in minutes at higher temperatures. The reduction appears to proceed from the rim of the crystal inward with time. The reduction appears initially rectilinear as if controlled by

  13. Constant average olivine Mg# in cratonic mantle reflects Archaean mantle melting to the exhaustion of orthopyroxene

    NASA Astrophysics Data System (ADS)

    Bernstein, S.; Kelemen, P. B.; Hanghoj, K.

    2006-12-01

    Shallow (garnet-free) cratonic mantle, occurring as xenoliths in kimberlites and alkaline basaltic lavas, has high Mg# (100x Mg/(Mg+Fe)>92) and is poor in Al and Ca compared to off-cratonic mantle. Many xenoliths show rhenium-depletion age of > 3 Ga, and are thus representative of depleted mantle peridotite that form an integral part of the stable nuclei of Archaean (2.5-3.8 Ga) cratons. Accordingly, the depleted composition of the xenolith suites is linked to Archaean melt extraction events. We have compiled data for many suites of shallow cratonic mantle xenoliths worldwide, including samples from cratons of Kaapvaal, Tanzania, Siberia, Slave, North China and Greenland, and encompassing both the classic orthopyroxene-rich peridotites of Kaapvaal and orthopyroxene-poor peridotites from Greenland. The suites show a remarkably small range in average olivine Mg# of 92.8 +/- 0.2. Via comparison with data for experimental melting of mantle peridotite compositions, we explain consistent olivine Mg# in the shallow cratonic mantle as the result of mantle melting and melt extraction to the point of orthopyroxene exhaustion, leaving a nearly monomineralic olivine, or dunitic, residue. Experimental data for peridotite melting at pressures less than 4 GPa and data on natural rocks suggest that mantle olivine has a Mg# of about 92.8 at the point of orthopyroxene exhaustion. If the melt extraction was efficient, no further melting could take place without a considerable temperature increase or melt/fluid flux through the dunite residue at high temperatures. While the high Mg#, dunite-dominated xenolith suites from e.g. Greenland represent simple residues from mantle melting, the orthopyroxene-rich xenolith suites with identical Mg# as known from e. g. Kaapvaal must reflect some additional processes. We envisage their derivation from dunite protoliths via subsequent melt/rock reaction with silica-rich melts or, in some cases, possibly as residues at higher average melting

  14. Genesis of zircon megacrysts in Cenozoic alkali basalts and the heterogeneity of subcontinental lithospheric mantle, eastern China

    NASA Astrophysics Data System (ADS)

    Yu, Yao; Xu, Xisheng; Chen, Xiaoming

    2010-09-01

    Zircon megacrysts are found in alluvial deposits associated with Cenozoic basalts from Changle in Shandong Province, Mingxi in Fujian Province and Penglai in Hainan Province within the coastal area of eastern China. They are colourless, transparent to light brown-maroon, and some of them are up to 16 mm long. U-Pb ages of zircon megacrysts from Changle, Mingxi and Penglai are 19.2 ± 0.7 Ma, 1.2 ± 0.1 Ma and 4.1 ± 0.2 Ma respectively, slightly older than the eruption ages of their corresponding host rocks (16.05-18.87 Ma, 0.9-2.2 Ma, 3 Ma). ɛHf(t) values of zircon megacrysts are 9.02 ± 0.49, 6.83 ± 0.47, 4.46 ± 0.48 for Changle, Mingxi and Penglai, respectively, which indicates their mantle origin. We suggest that the zircon megacrysts originated from metasomatised lithospheric mantle and were later brought up quickly by the host basaltic magma. The euhedral forms, uniform internal structure and chemical homogeneity within a single grain suggest crystallization under stable conditions. Pronounced positive Ce anomalies and negligible Eu anomalies suggest oxidizing conditions and little or no fractional crystallization of plagioclase. The differences in Hf-isotope compositions among the zircon megacrysts from different localities are consistent with the Sr-Nd-Pb isotopic compositions of their respective host basalts. This indicates that the host basalts acquired their isotopic signatures from the lithospheric mantle from which the zircon megacrysts derived. These data document the lateral compositional heterogeneity in the upper mantle beneath eastern China. Like mantle xenoliths, zircon megacrysts also have the potential to fingerprint the composition and evolution of the subcontinental lithospheric mantle.

  15. Origin of metaluminous and alkaline volcanic rocks of the Latir volcanic field, northern Rio Grande rift, New Mexico

    USGS Publications Warehouse

    Johnson, C.M.; Lipman, P.W.

    1988-01-01

    Volcanic rocks of the Latir volcanic field evolved in an open system by crystal fractionation, magma mixing, and crustal assimilation. Early high-SiO2 rhyolites (28.5 Ma) fractionated from intermediate compositionmagmas that did not reach the surface. Most precaldera lavas have intermediate-compositions, from olivine basaltic-andesite (53% SiO2) to quartz latite (67% SiO2). The precaldera intermediate-composition lavas have anomalously high Ni and MgO contents and reversely zoned hornblende and augite phenocrysts, indicating mixing between primitive basalts and fractionated magmas. Isotopic data indicate that all of the intermediate-composition rocks studied contain large crustal components, although xenocrysts are found only in one unit. Inception of alkaline magmatism (alkalic dacite to high-SiO2 peralkaline rhyolite) correlates with, initiation of regional extension approximately 26 Ma ago. The Questa caldera formed 26.5 Ma ago upon eruption of the >500 km3 high-SiO2 peralkaline Amalia Tuff. Phenocryst compositions preserved in the cogenetic peralkaline granite suggest that the Amalia Tuff magma initially formed from a trace element-enriched, high-alkali metaluminous magma; isotopic data suggest that the parental magmas contain a large crustal component. Degassing of water- and halogen-rich alkali basalts may have provided sufficient volatile transport of alkalis and other elements into the overlying silicic magma chamber to drive the Amalia Tuff magma to peralkaline compositions. Trace element variations within the Amalia Tuff itself may be explained solely by 75% crystal fractionation of the observed phenocrysts. Crystal settling, however, is inconsistent with mineralogical variations in the tuff, and crystallization is thought to have occurred at a level below that tapped by the eruption. Spatially associated Miocene (15-11 Ma) lavas did not assimilate large amounts of crust or mix with primitive basaltic magmas. Both mixing and crustal assimilation processes

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  17. Basaltic volcanism on the eucrite parent body - Petrology and chemistry of the polymict eucrite ALHA80102

    NASA Technical Reports Server (NTRS)

    Treiman, A. H.; Drake, M. J.

    1985-01-01

    The polymict eucrite meteorite ALHA80102 is an unequilibrated breccia of basaltic and gabbroic clasts in a fragmental matrix. Clasts include basalts of many textural types, cumulate gabbro, black 'glass', and ferroan troctolite (plagioclase, silica, Fe-rich olivine, ilmenite, mesostasis). Ferroan troctolite has not been previously reported from eucrites or howardites; it is interpreted as the end-product of fractional crystallization of eucritic magmas. Bulk and trace element compositions (by electron microprobe and INAA) of clasts and matrix from ALHA80102 are similar to those of other eucrites; the meteorite contains clasts similar to Juvinas and to Stannern. A clast of cumulate eucrite gabbro is enriched in the light rare earths (La/Lu = 2XCI). This clast is interpreted as an unrepresentative sample of metamorphically equilibrated gabbro; LREE-enriched magmas need not be invoked. ALHA80102 is similar to other polymict eucrites from the Allan Hills and may be paired with ALHA76005, ALHA77302, and ALHA78040.

  18. Source, evolution and emplacement of Permian Tarim Basalts: Evidence from U-Pb dating, Sr-Nd-Pb-Hf isotope systematics and whole rock geochemistry of basalts from the Keping area, Xinjiang Uygur Autonomous region, northwest China

    NASA Astrophysics Data System (ADS)

    Zhang, Dayu; Zhou, Taofa; Yuan, Feng; Jowitt, Simon M.; Fan, Yu; Liu, Shuai

    2012-04-01

    Permian basalts distribute at least 250,000 km2, and underlie the southwest Tarim Basin in Xinjiang Uygur Autonomous region, northwest China. This vast accumulation of basalt is the main part of the Tarim Large Igneous Province (LIP). The basaltic units in the Lower Permian Kupukuziman and Kaipaizileike Formations in the Keping area, Tarim Basin; were the best exposure of the Permian basalt sequence in the basin. LA-ICP-MS U-Pb dating of zircon from the basal basaltic unit in the section gives an age of 291.9 ± 2.2 Ma (MSWD = 0.30, n = 17); this age, combined with previously published geochronological data, indicates that the basalts in the Tarim Basin were emplaced between 292 Ma and 272 Ma, with about 90% of the basalts being emplaced between 292 and 287 Ma. Basalts from the Keping area have high FeOT (10.8-18.6 wt.%), low Mg#s (0.26-0.60), and exhibit primitive mantle normalized patterns with positive Pb, P and Ti but negative Zr, Y and Ta anomalies. The basalts from both formations have similar 206Pb/204Pb (18.192-18.934), 207Pb/204Pb (15.555-15.598) and 208Pb/204Pb (38.643-38.793) ratios. The basalts also have high ɛSr(t) (45.7-62.1), low ɛNd(t) (-3.6 to -2.2) and low zircon ɛHf(t) (-4.84 to -0.65) values. These characteristics are typical of alkali basalts and suggest that the basalts within the Tarim Basin were derived from an OIB-type mantle source and interacted with enriched mantle (EMI-type) before emplacement. Rare earth element systematics indicate that the parental melts for the basalts were high-degree partial melts derived from garnet lherzolite mantle at the base of the lithosphere. Prior to emplacement, the Tarim Permian Basalts (TPB) underwent fractional crystallization and assimilated crustal material; the basalts were finally emplaced during crustal extension in an intra-plate setting. The wide distribution, deep source and high degree partial melting of the TPB was consistent with a mantle plume origin. The TPB and other coeval igneous

  19. Vestas Pinaria Region: Original Basaltic Achondrite Material Derived from Mixing Upper and Lower Crust

    NASA Technical Reports Server (NTRS)

    Mcfadden, L. A.; Combe, Jean-Philippe; Ammannito, Eleonora; Frigeri, Alessandro; Stephan, Katrin; Longobardo, Andrea; Palomba, Ernesto; Tosi, Federico; Zambon, Francesca; Krohn, Katrin; hide

    2015-01-01

    Analysis of data from the Dawn mission shows that the Pinaria region of Vesta spanning a portion of the rim of the Rheasilvia basin is bright and anhydrous. Reflectance spectra, absorption band centers, and their variations, cover the range of pyroxenes from diogenite-rich to howardite and eucrite compositions, with no evidence of olivine in this region. By examining band centers and depths of the floor, walls and rims of six major craters in the region, we find a lane of diogenite-rich material next to howardite-eucrite material that does not follow the local topography. The source of this material is not clear and is probably ejecta from post-Rheasilvia impacts. Material of a howardite-eucrite composition originating from beyond the Rheasilvia basin is evident on the western edge of the region. Overall, the Pinaria region exposes the complete range of basaltic achondrite parent body material, with little evidence of contamination of non-basaltic achondrite material. With both high reflectance and low abundance of hydrated material, this region of Vesta may be considered the "Pinaria desert".

  20. Tracking the weathering of basalts on Mars using lithium isotope fractionation models

    PubMed Central

    Losa‐Adams, Elisabeth; Gil‐Lozano, Carolina; Gago‐Duport, Luis; Uceda, Esther R.; Squyres, Steven W.; Rodríguez, J. Alexis P.; Davila, Alfonso F.; McKay, Christopher P.

    2015-01-01

    Abstract Lithium (Li), the lightest of the alkali elements, has geochemical properties that include high aqueous solubility (Li is the most fluid mobile element) and high relative abundance in basalt‐forming minerals (values ranking between 0.2 and 12 ppm). Li isotopes are particularly subject to fractionation because the two stable isotopes of lithium—7Li and 6Li—have a large relative mass difference (∼15%) that results in significant fractionation between water and solid phases. The extent of Li isotope fractionation during aqueous alteration of basalt depends on the dissolution rate of primary minerals—the source of Li—and on the precipitation kinetics, leading to formation of secondary phases. Consequently, a detailed analysis of Li isotopic ratios in both solution and secondary mineral lattices could provide clues about past Martian weathering conditions, including weathering extent, temperature, pH, supersaturation, and evaporation rate of the initial solutions in contact with basalt rocks. In this paper, we discuss ways in which Martian aqueous processes could have lead to Li isotope fractionation. We show that Li isotopic data obtained by future exploration of Mars could be relevant to highlighting different processes of Li isotopic fractionation in the past, and therefore to understanding basalt weathering and environmental conditions early in the planet's history. PMID:27642264

  1. Mineralogy of interplanetary dust particles from the 'olivine' infrared class

    NASA Technical Reports Server (NTRS)

    Christoffersen, R.; Buseck, P. R.

    1986-01-01

    Analytical electron microscopy observations establish that olivine is abundant and the predominant silicate phase in three interplanetary dust particles (IDPs) from the 'olivine' infrared spectra category. Two of the particles have microstructures resembling those of most nonhydrous chondritic IDPs, consisting of micron to submicron grains together with a matrix composed of amorphous carbonaceous material and sub-500 A grains. In addition to olivine these particles respectively contain enstatite and magnetite, and pentlandite plus Ca-rich clinopyroxene. The third IDP consists mostly of olivine and pyrrhotite with little or no matrix material. Olivine grains in this particle contain prominent solar-flare ion tracks with densities corresponding to a space-exposure age between 1000 to 100,000 years. Although the three particles have olivine-rich mineralogies in common, other aspects of their mineralogies and microstructures suggest that they experienced different formation histories. The differences between the particles indicate that the olivine infrared spectral category is a diverse collection of IDPs that probably incorporates several genetic groups.

  2. Melting Conditions of Basaltic Volcanism from Collision to Escape in the Central Anatolian Volcanic Province

    NASA Astrophysics Data System (ADS)

    Maloney, P. M.; Reid, M. R.; Cosca, M. A.; Gencalioglu Kuscu, G.

    2013-12-01

    Both Miocene and Quaternary mafic volcanics have erupted in the vicinity of the present-day Central Anatolian fault zone since the cessation of Afro-Arabian subduction and continent-continent collision, and the initiation of tectonic escape. We report results for samples from the Central Anatolian Volcanic Province (near Hasan volcano) and the Sarkisla region of the Sivas basin (250 km NE of Hasandag) analyzed with the goal of understanding the melting conditions responsible for the post-collisional magmatism in these regions. New 40Ar/39Ar dates for basalts erupted near Hasan range in age from 2.58 +/- 0.08 Ma to 62 +/- 4 ka. A majority of the dates cluster at ~400 ka, ages similar to those documented by Notsu et al, 1995. These subalkaline basalts have Zn/Fe and FC3MS [(FeO*/CaO)-3x(MgO/SiO2)] concentrations (10.0-11.4 and 0.05-0.39, respectively) expected for basalts produced by melting of peridotite (Le Roux et al, 2011, Yang and Zhou, 2013). Using olivine-opx-melt thermobarometry (Lee et al, 2009), the samples are determined to have been extracted from the mantle at 1.2-1.8 GPa and 1314-1391 °C. Clinopyroxene thermobarometry (Putirka, 2003) shows that they then crystallized at 0.7 GPa and ~1200°C. Enrichments in LILE:HFSE, most likely imparted to the magmas from mantle lithosphere which has been enriched by previous subduction zone metasomatism, is present in all of the samples. Accordingly, basalts sampled near Hasan are derived from a shallow lithospheric mantle peridotite source that has been affected by Afro-Arabian subduction prior to collision. New 40Ar/39Ar dates for basanites and basalts from the Sarkisla region show that they erupted between 17.6 +/- 0.4 Ma and 14.09 +/- 0.09 Ma. They have elsewhere been reported to be Plio-Pleistocene in age (Parlak et al., 2001). Zn/Fe and FC3MS for these basalts (Zn/Fe: 10.4-12.6, FC3MS: 0.29-0.91) range to values above the maximum value produced by peridotite melts (~10.8 and 0.65, respectively). Therefore

  3. Early and Late Alkali Igneous Pulses and a High-3He Plume Origin for the Deccan Flood Basalts.

    PubMed

    Basu, A R; Renne, P R; Dasgupta, D K; Teichmann, F; Poreda, R J

    1993-08-13

    Several alkalic igneous complexes of nephelinite-carbonatite affinities occur in extensional zones around a region of high heat flow and positive gravity anomaly within the continental flood basalt (CFB) province of Deccan, India. Biotites from two of the complexes yield (40)Ar/(39)Ar dates of 68.53 +/- 0.16 and 68.57 +/- 0.08 million years. Biotite from a third complex, which intrudes the flood basalts, yields an (40)Ar/(39)Ar date of 64.96 +/- 0.1 1 million years. The complexes thus represent early and late magmatism with respect to the main pulse of CFB volcanism 65 million years ago. Rocks from the older complexes show a (3)He/(4)He ratio of 14.0 times the air ratio, an initial (87)Sr/(86)Sr ratio of 0.70483, and other geochemical characteristics similar to ocean island basalts; the later alkalic pulse shows isotopic evidence of crustal contamination. The data document 3.5 million years of incubation of a primitive, high-(3)He mantle plume before the rapid eruption of the Deccan CFB.

  4. Electron- and Photon-stimulated Desorption of Alkali Atoms from Lunar Sample and a Model Mineral Surface

    NASA Technical Reports Server (NTRS)

    Yakshinskiy, B. V.; Madey, T. E.

    2003-01-01

    We report recent results on an investigation of source mechanisms for the origin of alkali atoms in the tenuous planetary atmospheres, with focus on non-thermal processes (photon stimulated desorption (PSD), electron stimulated desorption (ESD), and ion sputtering). Whereas alkaline earth oxides (MgO, CaO) are far more abundant in lunar samples than alkali oxides (Na2O, K2O), the atmosphere of the Moon contains easily measurable concentrations of Na and K, while Ca and Mg are undetected there; traces of Ca have recently been seen in the Moon's atmosphere (10-3 of Na). The experiments have included ESD, PSD and ion sputtering of alkali atoms from model mineral surface (amorphous SiO2) and from a lunar basalt sample obtained from NASA. The comparison is made between ESD and PSD efficiency of monovalent alkalis (Na, K) and divalent alkaline earths (Ba, Ca).The ultrahigh vacuum measurement scheme for ESD and PSD of Na atoms includes a highly sensitive alkali metal detector based on surface ionization, and a time-of-flight technique. For PSD measurements, a mercury arc light source (filtered and chopped) is used. We find that bombardment of the alkali covered surfaces by ultraviolet photons or by low energy electrons (E>4 eV) causes desorption of hot alkali atoms. This results are consistent with the model developed to explain our previous measurements of sodium desorption from a silica surface and from water ice: electron- or photon-induced charge transfer from the substrate to the ionic adsorbate causes formation of a neutral alkali atom in a repulsive configuration, from which desorption occurs. The two-electron charge transfer to cause desorption of divalent alkaline eath ions is a less likely process.The data support the suggestion that PSD by UV solar photons is a dominant source process for alkalis in the tenuous lunar atmosphere.

  5. Search for Olivine Spectral Signatures on the Surface of Vesta

    NASA Technical Reports Server (NTRS)

    Palomba, E.; De Sanctis, M. C.; Ammannito, E.; Capaccioni, F.; Capria, M. T.; Farina, M.; Frigeri, A.; Longobardo, A.; Tosi, F.; Zambon, F.; hide

    2012-01-01

    The occurrence of olivines on Vesta were first postulated from traditional petrogenetic models which suggest the formation of olivine as lower crustal cumulates. An indirect confirmation is given by their presence as a minor component in some samples of diogenite meteorites, the harzburgitic diogenites and the dunitic diogenites, and as olivine mineral clasts in howardites. Another indication for this mineral was given by interpretations of groundbased and Hubble Space Telescope observations that suggested the presence of local olivine-bearing units on the surface of Vesta. The VIR instrument onboard the DAWN mission has been mapping Vesta since July 2011. VIR acquired hyperspectral images of Vesta s surface in the wavelength range from 0.25 to 5.1 m during Approach, Survey and High Altitude Mapping (HAMO) orbits that allowed a 2/3 of the entire asteroid surface to be mapped. The VIR operative spectral interval, resolution and coverage is suitable for the detection and mapping of any olivine rich regions that may occur on the Vesta surface. The abundance of olivine in diogenites is typically lower than 10% but some samples richer in olivine are known. However, we do not expect to have extensive exposures of olivine-rich material on Vesta. Moreover, the partial overlap of olivine and pyroxene spectral signatures will make olivine difficult to detect. Different spectral parameters have been used to map olivine on extraterrestrial bodies, and here we discuss the different approaches used, and develop new ones specifically for Vesta. Our new methods are based on combinations of the spectral parameters relative to the 1 and 2 micron bands (the most prominent spectral features of Vesta surface in the visible and the infrared), such as band center locations, band depths, band areas, band area ratios. Before the direct application to the VIR data, the efficiency of each approach is evaluated by means of analysis of laboratory spectra of HED meteorites, pyroxenes, olivines

  6. Composition and evolution of the eucrite parent body - Evidence from rare earth elements. [extraterrestrial basaltic melts

    NASA Technical Reports Server (NTRS)

    Consolmagno, G. J.; Drake, M. J.

    1977-01-01

    Quantitative modeling of the evolution of rare earth element (REE) abundances in the eucrites, which are plagioclase-pigeonite basalt achondrites, indicates that the main group of eucrites (e.g., Juvinas) might have been produced by approximately 10% equilibrium partial melting of a single type of source region with initial REE abundances which were chondritic relative and absolute. Since the age of the eucrites is about equal to that of the solar system, extensive chemical differentiation of the eucrite parent body prior to the formation of eucrites seems unlikely. If homogeneous accretion is assumed, the bulk composition of the eucrite parent body can be estimated; two estimates are provided, representing different hypotheses as to the ratio of metal to olivine in the parent body. Since a large number of differentiated olivine meteorites, which would represent material from the interior of the parent body, have not been detected, the eucrite parent body is thought to be intact. It is suggested that the asteroid 4 Vesta is the eucrite parent body.

  7. Cl, P2O5, U and Br associated with mineral separates from a low and a high Ti mare basalt

    NASA Technical Reports Server (NTRS)

    Jovanovic, S.; Reed, G. W., Jr.

    1980-01-01

    Low Ti basalt 12040 and high Ti basalt 75055 have approximately the same Cl/P2O5 ratio; the Cl is that remaining after a hot water leach. Pyroxene, plagioclase and ilmenite minerals separated from the basalts also tend to have this same Cl/P2O5 ratio. This is evidence that these major minerals do not control the ratio since Cl and P would not be expected to partition to the same extent into each mineral. Olivine appears to be a special case. It is proposed that the grains measured contained inclusions with leachable and P2O5-related Cl. Dilute acid leaches of whole rock and separated minerals have the same or nearly the same Cl/P2O5 ratios as the residual samples. Apatite and whitlockite were probably the phases leached. They must be constituents of the mesostasis and are present as microminerals or coatings on major mineral grains. The acid leach results imply little or no partition of Cl and P2O5 into major minerals.

  8. A scanning electron microscope study of olivine crystal surfaces

    NASA Technical Reports Server (NTRS)

    Olsen, E. J.; Grossman, L.

    1974-01-01

    SEM photographs were taken of euhedral olivine grains from the Murchison C2 chondrite and several terrestrial and lunar occurrences. In general, the crystal faces of the meteorite grains are rough and uneven, with irregular growth patterns. They are very similar to crystal faces on terrestrial olivine grains that formed by sublimation from a vapor phase. They are very different from the relatively smooth and featureless surfaces of magmatic olivine crystals that precipitated from igneous melts. Qualitatively, the surface morphology of the crystal supports the contention that many euhedral crystals of olivine in C2 meteorites condensed from a gas phase.

  9. The evolution of high-alumina basalts of the Klyuchevskoy volcano, Kamchatka, Russia, based on microprobe analyses of mineral inclusions

    NASA Astrophysics Data System (ADS)

    Ozerov, Alexei Y.

    2000-01-01

    The origin of calc-alkaline high-alumina basalts (HAB) of the Klyuchevskoy volcano, Kamchatka, was examined using electron microprobe analyses of phenocrysts and mineral phases included in the phenocrysts. Continuous trends on major-element variation diagrams suggest the HAB were derived from high-magnesia basalt (HMB) by fractional crystallization. Phenocrysts in the HAB are strongly zoned: olivine (Mg# 91-64), clinopyroxene (Wo 45-38En 40-51Fs 5-20) and chrome—spinel/magnetite inclusions in them (Cr 2O 3 45-0 wt.%, TiO 2 0.5-11%). Microprobe analyses of minerals included in the phenocrysts provide additional constraints on the mineral crystallization trends in the HAB. Fe/Mg partitioning data, when applied to the phenocrysts cores, show they crystallized from a HMB. The similarity of phenocryst core compositions in HAB with those in HMB strongly suggests a genetic relationship between the two magma types.

  10. Effects of fO2, fH2O and aoxide on formation and density of extended planar defects in olivine

    NASA Astrophysics Data System (ADS)

    Burgess, K.; Cooper, R. F.

    2011-12-01

    Melt inclusions are used in geochemistry to inform our understanding of many physiochemical processes taking place in the mantle, such as melting, melt-rock interactions and magma mixing. Fundamental to this interpretation of melt inclusions is the assumption that they act as closed systems, i.e., they are chemically isolated after trapping and preserve primitive magma compositions. However, recent work indicates that volatiles (e.g., H and F) can be rapidly reset [Portnyagin et al., 2008], and the diffusion mechanisms and rates in tracer diffusion experiments, specifically of REEs, are a matter of some debate [Spandler and O'Neill, 2010; Cherniak, 2010]. The compendium of observations and experiments suggests a role of planar extended defects in effecting and affecting diffusion kinetics in olivine. Planar extended defects are the exothermic condensation of charged point defects into two-dimensional structures, their third dimension insufficient (i.e., sub-unit cell) to describe them as a unique phase. These planar defects, in a manner similar to mechanisms of "pipe" diffusion along dislocations and of grain boundary diffusion, can lead to measured diffusivities far greater than the lattice diffusivity, and their overall effect on flux is proportional to their spatial density [cf. Hart, 1957]. High-resolution TEM and AEM investigation of experimental olivine-basalt samples show the presence of planar defects near the olivine-melt interface, with the area fraction of the high-contrast defects in the images being greatest at high fO2 and/or fH2O while temperature has an effect on the defect dimensions but not total areal density. EDS analysis of the interface regions indicate high Ti/Ca and Ti/Al ratios compared to the glass; the stability of intercalated humite-type defects in olivine, a planar defect type found in some natural olivines [e.g., Risold et al., 2001; Hermann et al., 2007], is increased to higher temperature by the incorporation of Ti. Activities of

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

    USGS Publications Warehouse

    Church, S.E.; Tatsumoto, M.

    1975-01-01

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

  12. Insights into the origin of low- δ18O basaltic magmas in Hawaii revealed from in situ measurements of oxygen isotope compositions of olivines

    NASA Astrophysics Data System (ADS)

    Wang, Zhengrong; Eiler, John M.

    2008-05-01

    In situ measurements of oxygen isotope and elemental compositions of olivines from subaerial Mauna Kea lavas reveal that their δ18O values correlate positively with their forsterite contents, consistent with addition of one or more low- δ18O components into magmas from which they grew over the course of their crystallization-differentiation histories. This result supports previous suggestions that low- δ18O components to Mauna Kea lavas are contaminants derived from hydrothermally-altered rocks in the volcanic edifice or lithosphere, rather than components of the underlying mantle sources of these lavas. The slope of the correlation between δ18O values and forsterite contents of olivines is steeper for subaerial Mauna Kea lavas than for submarine Mauna Kea lavas, and olivines from Mauna Loa lavas exhibit negligible changes in δ18O values over a similar range of forsterite contents. Models of assimilation-fractional crystallization (AFC) processes can explain our observations if the δ18O values of crustal contaminants decrease sharply at the submarine-subaerial transition in Mauna Kea volcano, and if Mauna Loa lavas are either uncontaminated or contaminated only by rocks that have δ18O values similar to that of primary Mauna Loa magmas. We suggest that the differences in oxygen isotope systematics among Mauna Loa, submarine Mauna Kea and subaerial Mauna Kea lavas principally reflect the sources and amounts of water available to hydrothermal systems in the volcanic edifice.

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

    NASA Astrophysics Data System (ADS)

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

    2018-01-01

    This study presents a comprehensive analysis of the major and trace element, mineral, and Sr, Nd, Pb and Mg isotopic compositions of late Cenozoic intraplate basaltic rocks from central and southern Vietnam. The Sr, Nd, and Pb isotopic compositions of these basalts define a tight linear array between Indian mid-ocean-ridge basalt (MORB)-like mantle and enriched mantle type 2 (EM2) components. These basaltic rocks contain low concentrations of CaO (6.4-9.7 wt%) and have high Fe/Mn ratios (> 60) and FeO/CaO-3MgO/SiO2 values (> 0.54), similar to partial melts derived from pyroxenite/eclogite sources. This similarity is also supported by the composition of olivine within these samples, which contains low concentration of Ca and high concentrations of Ni, and shows high Fe/Mn ratios. The basaltic rocks have elevated Dy/Yb ratios that fall within the range of melts derived from garnet lherzolite material, although their Yb contents are much higher than those of modeled melts derived from only garnet lherzolite material and instead plot near the modeled composition of eclogite-derived melts. The Vietnamese basaltic rocks have lighter δ26Mg values (- 0.38 ± 0.06‰) than is expected for the normal mantle (- 0.25 ± 0.07‰), and these values decrease with decreasing Hf/Hf* and Ti/Ti* ratios, indicating that these basalts were derived from a source containing carbonate material. On primitive mantle-normalized multi-element variation diagrams, the central Vietnamese basalts are characterized by positive Sr, Eu, and Ba anomalies. These basalts also plot within the pelagic sediment field in Pbsbnd Pb isotopic space. This suggests that the mantle source of the basalts contained both garnet peridotite and recycled oceanic crust. A systematic analysis of variations in geochemical composition in basalts from southern to central Vietnam indicates that the recycled oceanic crust (possibly the paleo-Pacific slab) source material contains varying proportions of gabbro, basalt, and

  14. Vaporization Studies of Olivine via Knudsen Effusion Mass Spectrometry

    NASA Technical Reports Server (NTRS)

    Costa, G. C. C.; Jacobson, N. S.

    2014-01-01

    Olivine is the major mineral in the Earth's upper mantle occurring predominantly in igneous rocks and has been identified in meteorites, asteroids, the Moon and Mars. Among many other important applications in planetary and materials sciences, the thermodynamic properties of vapor species from olivine are crucial as input parameters in computational modelling of the atmospheres of hot, rocky exoplanets (lava planets). There are several weight loss studies of olivine vaporization in the literature and one Knudsen Effusion Mass Spectrometry (KEMS) study. In this study, we examine a forsterite-rich olivine (93% forsterite and 7% fayalite, Fo93Fa7) with KEMS to further understand its vaporization and thermodynamic properties.

  15. Chemical profiles along olivine crystallographic axes: a record of the melt-rock interaction sequence forming Hole U1309D Olivine-rich troctolites (Atlantis Massif, MAR, 30°N)

    NASA Astrophysics Data System (ADS)

    Ferrando, Carlotta; Godard, Marguerite; Ildefonse, Benoit; Rampone, Elisabetta

    2017-04-01

    The gabbroic section drilled at IODP Hole U1309D (Mid-Atlantic Ridge, IODP Expeditions 304, 305) comprises a whole range of modes from primitive olivine-rich troctolites to evolved gabbros. These series occur as discrete alternating intervals of variable composition and thickness at different depths. High MgO contents and a relatively large proportion of olivine-rich lithologies (up to 90% modal olivine) characterize this gabbroic section. Contacts between olivine-rich troctolites and neighboring coarse grained olivine gabbros are sharp, with the exception of the contacts between olivine-rich intervals and cross-cutting gabbroic veins, which are diffuse and characterized by progressive variations in plagioclase content. Olivine-rich troctolites are heterogeneously distributed along the borehole and show variable modal composition: centimeter to decimeter scale dunitic (90% olivine), troctolitic (enriched in plagioclase) and wehrlitic (enriched in clinopyroxene) domains were identified. Previous in-situ trace element geochemistry and crystallographic preferred orientation measurements of olivine-rich troctolites indicated that they record extensive melt impregnation of pre-existing olivine-rich material, either mantle rocks or dunitic cumulate. We performed a detailed multi-scale petro-structural and geochemical study on selected samples of well-preserved olivine-rich troctolites with the aim to unravel the sequence of re-equilibration processes and better constrain the local conditions driving the formation of these rocks. Processed EBSD maps show variable textures at single sample scale. All identified domains are characterized by coarse grained and deformed olivines, and small rounded undeformed olivines. Coarse grained and small rounded olivines have the same major and trace element compositions. Small olivines are interpreted as relicts after dissolution of coarse grained olivines. Clinopyroxene, plagioclase, and minor orthopyroxene are present as interstitial

  16. Electrolytic method to make alkali alcoholates using ion conducting alkali electrolyte/separator

    DOEpatents

    Joshi, Ashok V [Salt Lake City, UT; Balagopal, Shekar [Sandy, UT; Pendelton, Justin [Salt Lake City, UT

    2011-12-13

    Alkali alcoholates, also called alkali alkoxides, are produced from alkali metal salt solutions and alcohol using a three-compartment electrolytic cell. The electrolytic cell includes an anolyte compartment configured with an anode, a buffer compartment, and a catholyte compartment configured with a cathode. An alkali ion conducting solid electrolyte configured to selectively transport alkali ions is positioned between the anolyte compartment and the buffer compartment. An alkali ion permeable separator is positioned between the buffer compartment and the catholyte compartment. The catholyte solution may include an alkali alcoholate and alcohol. The anolyte solution may include at least one alkali salt. The buffer compartment solution may include a soluble alkali salt and an alkali alcoholate in alcohol.

  17. Evidence for melt partitioning between olivine and orthopyroxene in partially molten harzburgite

    NASA Astrophysics Data System (ADS)

    Miller, K.; Zhu, W.; Montesi, L. G.; Le Roux, V.; Gaetani, G. A.

    2013-12-01

    During melting at mid-ocean ridges, melt is driven into an equilibrium, minimum-energy configuration by surface energy gradients between solid-solid and solid-liquid phase boundaries. Such a configuration, where melt is mostly restricted to three and four-grain junctions, acts as a porous medium through which melt can percolate to the surface. For a monomineralic system, melt is distributed evenly among all grains. However, in mineralogical heterogeneous systems, melt partitions unevenly between the various solid phases to minimize the total energy of the system. In a ocean ridge melting environment, where olivine is often juxtaposed against orthopyroxene (opx), lithologic partitioning is expected to turn olivine-rich regions into high-permeability conduits, through which melt can be quickly extracted, drastically increasing the permeability of the mantle [Zhu and Hirth, 2003]. Lithologic partitioning has been demonstrated in experiments using analogue systems [Watson, 1999]; however, to date, no experiment has confirmed its existence in partially molten mantle systems. We present experimental results that determine the degree of melt partitioning between olivine and opx in partially molten harzburgites. Samples were prepared from a powdered mixture of oxides and carbonates and then hot-pressed in a solid-media piston-cylinder apparatus at 1350°C and 1.5GPa [Zhu et al., 2011] to achieve an 82/18 vol. % ratio of olivine to opx. Prior to hot-pressing, basalt was added to the powdered mixtures in various proportions to test for lithologic partitioning across a range of melt fractions. Three-dimensional, 700nm-resolution images of our samples were obtained using synchrotron X-ray microtomography on the 2BM station of the Advanced Photon Source at Argonne National Labs. Image data were filtered using an anisotropic diffusion filter to enhance phase contrast and then segmented to produce binary representations of each phase. In order to quantitatively demonstrate

  18. Back-arc with frontal-arc component origin of Triassic Karmutsen basalt, British Columbia, Canada

    USGS Publications Warehouse

    Barker, F.; Sutherland, Brown A.; Budahn, J.R.; Plafker, G.

    1989-01-01

    by first mixing primitive arc magma with enriched basaltic liquid derived either from garnet peridotite or metasomatized mantle, followed by fractionation of olivine, pyroxenes, plagioclase and spinel. ?? 1989.

  19. Olivine Instability: An Experimental View of Mechanism of Deep Earthquakes

    NASA Astrophysics Data System (ADS)

    Long, H.; Weidner, D.; Li, L.; Chen, J.; Wang, L.

    2007-12-01

    Olivine (¦Á-(Mg,Fe)2SiO4) is the major constituent of the upper mantle and the ocean lithosphere. In subduction zone, where the earthquakes happen, the rheology of slab is mainly controlled by that of olivine. Several different mechanisms for deep focus earthquakes have been suggested, which include olivine instability (Bridgman, 1936; Orowan, 1960; Post, 1977; Ogawa, 1987; Hobbs and Ord, 1988; Kao and Chen, 1995), shear-induced melting (Griggs, 1954, 1972; Griggs and Handin, 1960; Griggs and Baker, 1969), phase transformation (Bridgman, 1945; Benioff, 1963; Meade and Jeanloz, 1989), dehydration of hydrous specimens (Meade and Jeanloz, 1991), and olivine metastability-induced anticrack (Green and Houston, 1995). Since the low temperature of the ¡°cold¡± slab, which can be as low as 600¡ãC in transition zone, olivine may still exist there and thus its shear instability may still be the possible mechanism for the deep-focus earthquakes. In our experimental study on deformation of San Carlos olivine at subduction zone conditions carried out on a D-DIA apparatus, Sam85 at X17B2, NSLS, we observed that the transitional temperature between regimes of insensitive to temperature and sensitive to temperature can be as high as 900¡ãC or even higher for the annealed polycrystal olivine sample, while that for unannealed sample can be as low as 450¡ãC. Our results for the unannealed sample are consistent to the result of Raterron et al (2004), which is concluded from the relaxation experiments. The annealed and unannealed olivine can be present the natural olivine in non-fault systems and that in pre-existing fault systems in subduction zone, respectively. We therefore propose a new olivine instability model with a ¡°sandwich¡± formation for the deep focus earthquakes: In this model the pre-existing fault system is surrounded by the no-fault systems. When the slab dives down, the olivine in both systems undergoes a stress- build-up process and can hold very high

  20. Paraná-Etendeka basalts in Misiones, Argentina; characterization and petrogenetic inferences

    NASA Astrophysics Data System (ADS)

    Rämö, O. T.; Heikkilä, P. A.

    2013-12-01

    The Early Cretaceous (ca. 130 Ma) Paraná-Etendeka flood basalts constitute one of the major Phanerozoic LIP sequences with an original volume probably in excess of 2.3 Mkm3.The bulk of this volcanic system is preserved in South America (Brazil, Uruguay, Paraguay, Argentina), where it manifests the onset of South Atlantic opening at present 25 degrees Southern Latitude. The sequence is overwhelmingly basaltic (ca. 90%), but also includes contemporaneous silicic volcanic rocks. Known as the Serra Geral Suite (e.g., Bellieni et al., 1984), it fills the Paraná Basin with a northward deepening strata of lavas with a maximum thickness of ca. 1500 m. We have collected and examined basalt samples from the west-central part (western flank) of the Paraná Basin in Misiones State, northeastern Argentina (54-55 degrees Western Longitude), where the estimated thickness of the basalt succession decreases from ca. 700 m in the east to ca. 300 m in the west. The examined samples are massive, aphyric (or microphyric with plagioclase and altered olivine microphenocrysts), and geochemically relatively evolved (Mg number 50-35) basalts and basaltic andesites. Their MgO values are between 6 and 3.7 wt.% and Ni content is relatively low (65-20 ppm). Incompatible trace element values increase with increasing fractionation (decreasing Mg number), e.g., Zr from 135 to 290 ppm, Ce from 45 to 105 ppm, Nd from 20 to 50 ppm, Sm from 5 to 11 ppm, Ba from 280 to 600 ppm, and Y from 25 to 50 ppm. In terms of Ti, the samples fall into two groups (1.9-2.3 and ca. 3.8 wt.% TiO2). These values conform, respectively, to the high-Ti, high-Ti/Y Paranapanema and Pitanga magma types of Peate et al. (1992) that govern the northern half of the Paraná basalt succession. Initial Nd and Sr isotope compositions of the two groups are remarkably uniform. Our analyzed ten samples have an average initial (at 134.6 Ma) epsilon-Nd value of -4.2 × 0.3 (1 SD) and an average initial 87Sr/86Sr of 0.70570 × 0

  1. Impact ionisation mass spectrometry of platinum-coated olivine and magnesite-dominated cosmic dust analogues

    NASA Astrophysics Data System (ADS)

    Hillier, Jon K.; Sternovsky, Z.; Kempf, S.; Trieloff, M.; Guglielmino, M.; Postberg, F.; Price, M. C.

    2018-07-01

    Impact ionisation mass spectrometry enables the composition of cosmic dust grains to be determined in situ by spacecraft-based instrumentation. The proportion of molecular ions in the impact plasma is a function of the impact velocity, making laboratory calibration vital for the interpretation of the mass spectra, particularly at the low velocities typical of lunar or asteroid encounters. Here we present an analysis of laboratory impact ionisation mass spectra from primarily low (<15 km s-1) velocity impacts of both olivine and magnesite-dominated particles onto the SUrface Dust Mass Analyzer (SUDA) laboratory mass spectrometer. The cation mass spectra show characteristic peaks due to their constituent elements, with Mg, Al, Si, C, Ca, O and Fe frequently present. Contaminant species from the conductive coating process (B, Na, K, C, Pt) also occur, at varying frequencies. Possible saponite or talc inclusions in the magnesite particles are revealed by the presence of Si, Fe, Ca and Al in the magnesite mass spectra. Magnesium is clearly present at the lowest impact velocities (3 km s-1), at which alkali metals were presumed to dominate. Peaks attributed to very minor amounts of water or hydroxyl present in the grains are also seen at low velocities in both cation and anion mass spectra, demonstrating the feasibility of impact ionisation mass spectrometry in identifying hydrated or hydrous minerals, during very low velocity encounters or with very low abundances of water or hydroxy groups, in the impinging grains. Velocity thresholds for the reliable identification of the major elements within the magnesite and olivine cation spectra are presented. Additionally, relative sensitivity factors for Mg (5.1), Fe (1.5) and O (0.6) with respect to Si, in the olivine particles, at impact speeds >19 km s-1, were found to be very similar to those previously determined for orthopyroxene-dominated particles, despite different target and projectile materials. This confirms that

  2. The influence of magma degassing on entrapment pressures recorded in olivine-hosted melt inclusions

    NASA Astrophysics Data System (ADS)

    Gaetani, G. A.

    2013-12-01

    The concentrations of H2O and CO2 in olivine-hosted melt inclusions provide estimates for the pressures at which they were entrapped, and represent an important source of information on the depths at which basaltic magmas crystallize [1]. Results from recent dehydration experiments demonstrate that diffusive loss of H2O from melt inclusions, driven by degassing of the external magma, leads to significant decreases to pressure within the inclusion [2, 3]. This, in turn, lowers the solubility of CO2 in the included melt causing a vapor to exsolve and form a bubble. This process has the potential to significantly modify estimates of entrapment pressures derived from volatile concentrations in olivine hosted melt inclusions. I have developed a quantitative model that describes this process, allowing the influence of degassing on entrapment pressures to be rigorously evaluated. Diffusive loss of H2O from the inclusions was determined using the model of [3]. An equation of state (EOS) for the silicate melt was taken from the results of [4] and [5], while the EOS for H2O-CO2 vapor was taken from [6]. The solubilities of H2O and CO2 in the silicate melt were derived from VolatileCalc [7]. Modeling results demonstrate that degassing of H2O-rich magma produces significant pressure drops, so that entrapment pressures never exceed crustal values and always represent a minimum. Conversely, degassing of H2O-poor magma does not significantly perturb the H2O content of olivine-hosted melt inclusions. Therefore, these inclusions preserve reliable records of the pressures at which they were entrapped. These results are consistent with a global compilation of olivine-hosted melt inclusion entrapment pressures presented by [3]. References: [1] Wanless, VD, and Shaw, AM, Nature Geosci, 5, 651-655 (2012); [2] Gaetani, GA, et al., Geology, 40, 915-918 (2012); [3] Bucholz, CE, et al., Earth Planet Sci Lett, 374, 145-155 (2013); [4] Lange, R. A., and Carmichael, ISE, Geochim Cosmochim Acta

  3. Phase equilibria modeling in igneous petrology: use of COMAGMAT model for simulating fractionation of ferro-basaltic magmas and the genesis of high-alumina basalt

    NASA Astrophysics Data System (ADS)

    Ariskin, Alexei A.

    1999-05-01

    A new version of COMAGMAT-3.5 model designed for computer simulations of equilibrium and fractional crystallization of basaltic magmas at low to high pressures is presented. The most important modifications of COMAGMAT include an ability to calculate more accurately the crystallization of magnetite and ilmenite, allowing the user to study numerically the effect of oxygen fugacity on basalt magma fractionation trends. Methodological principles of the use of COMAGMAT were discussed based on its thermodynamical and empirical basis, including specific details of the model calibration. Using COMAGMAT-3.5 a set of phase equilibria calculations (called Geochemical Thermometry) has been conducted for six cumulative rocks from the Marginal Border Series of the Skaergaard intrusion. As a result, initial magma temperature (1165±10°C) and trapped melt composition proposed to be parental magma to the Skaergaard intrusion were determined. Computer simulations of perfect fractionation of this composition as well as another proposed parent produced petrochemical trends opposite to those followed from natural observations. This is interpreted as evidence for an initial Skaergaard magma containing a large amount of olivine and plagioclase crystals (about 40-45%), so that the proposed and calculated parents are related through the melt trapped in the crystal-liquid mixture. This promotes the conclusion that the Skaergaard magma fractionation process was intermediate between equilibrium and fractional crystallization. In this case the classic Wager's trend should be considered an exception rather than a rule for the differentiation of ferro-basaltic magmas. A polybaric version of COMAGMAT has been applied for the genetic interpretation of a volcanic suite from the Klyuchevskoi volcano, Kamchatka, Russia. To identify petrological processes responsible for the observed suite ranging from high-magnesia to high-alumina basalts, we used the model to simulate the Klyuchevskoi suite

  4. A Geochemical and Mineralogical Model for Formation of Layered Sulfate Deposits at Meridiani Planum by Hydrothermal Acid-sulfate Alteration of Pyroclastic Basalt

    NASA Astrophysics Data System (ADS)

    McCollom, T. M.; Hynek, B. M.

    2012-12-01

    The Mars Exploration Rover (MER) Opportunity has extensively characterized sulfate-rich, hematite-bearing bedrock exposed at Meridiani Planum, Mars. Based on various measurements, the mineral composition of the bedrocks has been interpreted to include: amorphous silica/glass/phyllosilicates, Mg-, Ca-, and Fe-bearing sulfates including jarosite, minor amounts of igneous phases including plagioclase, pyroxene, olivine, and magnetite, and hematite [1,2]. Chemically, the bedrocks closely resemble the composition of pristine martian basalt with addition of S and O, and minor variations of Mg and Cl with depth [3,4]. Based on these and other observations, the MER team has proposed that the bedrocks represent chemically altered siliciclastic sediments combined with sulfate salts formed by evaporation of sulfate-bearing fluids, modified by transport and multiple stages of infiltrating groundwater [3,5]. Several alternative scenarios have been proposed for the origin of the rocks including large impacts [6], evaporating glacial deposits [7], acid-fog alteration [8], and hydrothermal acid-sulfate alteration of basalt [4]. In order to further evaluate the potential contribution of hydrothermal proceeses to the deposits, we performed numerical geochemical models of acid-sulfate alteration of martian basalt based on constraints provided by recent laboratory experiments. Experimental studies of alteration of basalt conducted in our lab [9] indicate that the initial stages of acid-sulfate alteration of pyroclastic basalt are characterized by rapid decomposition of igneous crystalline phases including plagioclase, pyroxene, and olivine, while the glass (and igneous phases protected within the glass) remain unreactive. Elements released by dissolving minerals are precipitated primarily as amorphous silica and Ca-, Al-, Fe- and Mg-bearing sulfates, while precipitation of phyllosilicates and Fe-oxides/oxyhydroxides (FeOx) is kinetically inhibited. Based on these constraints, models

  5. Microtubules in basalt glass from Hawaii Scientific Driling Project #2 phase 1 core and Hilina slope, Hawaii: evidence of the occurrence and behavior of endolithic microorganisms.

    PubMed

    Walton, A W

    2008-08-01

    Elongate, fine tubes, approximately 1 microm wide and up to 200 microm long, extend from fractured surfaces, vesicle walls, and internal fractures into fragments of basalt glass in samples from the Hawaii Scientific Drilling Project #2 phase 1 (HSDP #2(1)) core and the Hilina slope, Hawaii. Several features indicate that these tubes are microbial endolithic microborings: the tubes resemble many described microborings from oceanic basalt glass, their formation is postdepositional but restricted to certain but different ranges of time in the two sets of samples, and they are not uniformly distributed throughout glass fragments. Microtubules record several characteristic behaviors including boring into glass, mining, seeking olivine, and avoiding plagioclase. They also are highly associated with a particular form of glass-replacing smectite. Evidence of behavior should join morphological and geochemical criteria in indicating microbial alteration of basalt glass. In some samples, steeply conical tubes, approximately 10-20 microm in diameter tapering to 1 microm and commonly filled with smectite, appear to be modifications or elaborations of the microtubules. These also curve toward olivine and are associated with replacement smectite. In HSDP #2(1) samples, microtubules initiated at margins of shards before palagonite replaced those margins and are preserved during palagonitization. In fact, microtubules appear to have provided routes that enhanced the efficiency of water's reaching of unaltered glass. In Hilina Slope samples, the microtubules appear to postdate palagonitization because they initiate at the boundary between palagonite and unaltered sideromelane. Preservation of microtubules during palagonitization in samples together with recognition of other associated characteristics representing behavior suggests that such features may be recognizable in more heavily altered ancient rocks.

  6. Evaluation of olivine refractories for TES

    NASA Astrophysics Data System (ADS)

    Gay, B. M.; Cochrane, R. L.; Palmour, H., III; Paisley, M. J.

    1982-02-01

    The principal objectives of this program are to (1) experimentally determine the degree of improvement in thermal and mechanical performance that can be obtained with an olivine thermal storage brick made of domestic materials using advanced processing techniques compared with state-of-the-art as represented by commercial European bricks, (2) conduct an assessment of existing German ceramic process technology and determine its adaptability to domestic raw materials and manufacturing practices, and (3) investigate, on a limited basis, method for further improvement of domestic-olivine brick. To date, accomplishments include (1) installation of improved, computer-based instrumentation, (2) the use of this system to determine performance characteristics of a set of heat storage refractories under cyclic use conditions, (3) acquisition of the services of a knowledgeable European consultant, (4) continued lab-scale process/property optimization studies, and (5) comparative testing of olivine-based and magnesite-based heat storage refractories in the calorimetric test facility at Purdue University.

  7. Chemical characterization, nano-particle mineralogy and particle size distribution of basalt dust wastes.

    PubMed

    Dalmora, Adilson C; Ramos, Claudete G; Oliveira, Marcos L S; Teixeira, Elba C; Kautzmann, Rubens M; Taffarel, Silvio R; de Brum, Irineu A S; Silva, Luis F O

    2016-01-01

    Understanding the geochemistry of basalt alteration is central to the study of agriculture systems. Various nano-minerals play an important role in the mobilization of contaminants and their subsequent uptake by plants. We present a new analytical experimental approach in combination with an integrated analytical protocol designed to study basalt alteration processes. Recently, throughout the world, ultra-fine and nano-particles derived from basalt dust wastes (BDW) during "stonemeal" soil fertilizer application have been of great concern for their possible adverse effects on human health and environmental pollution. Samples of BDW utilized were obtained from companies in the Nova Prata mining district in southern Brazil for chemical characterization and nano-mineralogy investigation, using an integrated application of advanced characterization techniques such as X-ray diffraction (XRD), High Resolution-Transmission Electron microscopy (HR-TEM)/Energy Dispersive Spectroscopy (EDS)/(selected-area diffraction pattern) SAED, Field Emission-Scanning Electron Microscopy (FE-SEM/EDS), and granulometric distribution analysis. The investigation has revealed that BDW materials are dominated by SiO2, Al2O3, and Fe2O3, with a complex micromineralogy including alkali feldspar, augite, barite, labradorite, hematite, heulandrite, gypsum, kaolinite, quartz, and smectite. In addition, we have identified a number of trace metals such as Cd, Cu, Cr, and Zn, that are preferentially concentrated into the finer, inhalable, dust fraction and, thus, could present a health hazard in the urban areas around the basalt mining zone. The implication of this observation is that use of these nanometric-sized particulates as soil fertilizer may present different health challenges to those of conventional fertilizers, inviting future work regarding the relative toxicities of these materials. Our investigation on the particle size distribution, nano-particle mineralogy and chemical composition in

  8. Diffusional creep of fine-grained olivine aggregates: Chemical and melt effects

    NASA Astrophysics Data System (ADS)

    Yabe, K.; Hiraga, T.

    2017-12-01

    Since olivine is the major constituent mineral of the earth's upper mantle, flow properties of the upper mantle are often estimated based on flow laws of olivine aggregate which are determined by high-temperature creep experiments. Recently, Miyazaki et al. (2013) showed that crystallographic preferred orientation (CPO) which has been interpreted as the main cause for seismic wave anisotropy in mantle asthenosphere could be formed in diffusional creep regime. The detail of diffusional creep of olivine aggregates is not clear yet. The strength of olivine aggregates synthesized using sol-gel method (Faul and Jackson 2007) was more than one order of magnitude harder in viscosity than those synthesized from natural mantle rocks (Hirth and Kohlstedt 1995, Hansen et al. 2011) even at the same experimental conditions. This discrepancy can be interpreted by a presence of melt and/or impurity. The purpose of this study is to examine the effects of chemical composition and presence of the melt phase on the creep properties of olivine aggregates. At first, Fe-bearing olivine aggregates were prepared by vacuum sintering of nano-sized olivine powder synthesized from highly pure and fine-grained (<100 nm) source powders. Samples with and without dopants of Al2O3 and CaO were prepared. Then uniaxial compression tests at 1 atm were conducted. Deformation experiments showed that all the samples were deformed by diffusional creep mechanism. Both doped and non-doped samples exhibited sample strength at low temperature (=1150˚C), while the doped sample became significantly weaker with showing higher temperature sensitivity compared to non-doped samples at higher temperature. The temperature sensitivity of doped samples didn't change below and above solidus, which indicate the weakening due to chemical effect, not by the melting. Non-doped samples exhibits essentially the same strength as olivine aggregates synthesized from sol-gel method (Faul and Jackson 2007), while doped sample is

  9. The Mn-Fe negative correlation in olivines in ALHA 77257 ureilite

    NASA Technical Reports Server (NTRS)

    Miyamoto, M.; Furuta, T.; Fujii, N.; Mckay, D. S.; Lofgren, G. E.; Duke, M. B.

    1993-01-01

    An electron probe microanalyzer is used to measure the Mn, Fe, and oxygen zoning profiles of olivines in the ALHA 77257 ureilite. This is done to study the effects of reduction on the Mn-Fe value, as ureilite olivines exhibit thin reduced rims. Since the Mn content gradually increases toward the rim of ureilite olivines, while the Fa (= 100 x Fe/(Mg + Fe), mol percent) component decreases, the Mn-Fe content of olivine is likely related to redox conditions. The results of melting experiments suggest that the Mn-Fe positive correlation is related to temperature and that the negative correlation of Mn-Fe in olivine and low-Ca pyroxene is related to reduction.

  10. Experimentally determined subsolidus metal-olivine element partitioning with applications to pallasites

    NASA Astrophysics Data System (ADS)

    Donohue, Patrick H.; Hill, Eddy; Huss, Gary R.

    2018-02-01

    Pallasite meteorites, which consist primarily of olivine and metal, may be remnants of disrupted core-mantle boundaries of differentiated asteroids or planetesimals. The early thermal histories of pallasites are potentially recorded by minor- and trace-element zonation in olivine. However, constraining this history requires knowledge of element behavior under the conditions of pallasite formation, which is lacking for many of the main elements of interest (e.g., Co, Cr, Mn). In this study, we experimentally determined metal/olivine partition coefficients for Fe, Ni, Co, Cr, and Mn in a pallasite analogue at subsolidus temperatures. Metal/olivine partition coefficients (KM) increase in the order KMn < KCr < 1 < KFe < KCo < KNi, with five orders of magnitude separating KMn from KNi. Transition metals also become more siderophile with increasing experimental temperature (900-1550 °C). The experiments incidentally produced diffusion profiles in olivine for these elements; our results suggest they diffuse through olivine at similar rates. Core compositions of pallasite olivines are consistent with high-temperature equilibration with FeNi-metal. Olivine zonation toward crystal rims varies significantly for the investigated transition metals. We suggest rim zonation results from partial re-equilibration during late stage crystallization of minor phases (e.g., chromite, phosphates). This re-equilibration occurred over short timescales relative to overall pallasite cooling, likely tied to initial cooling rates on the order of 100-300 °C/Myr.

  11. Planetary basalts - Chemistry and petrology

    NASA Technical Reports Server (NTRS)

    Papike, J. J.; Bence, A. E.

    1979-01-01

    Recent literature (1975-1978) on planetary basalts is reviewed. Terrestrial basalts are considered in relation to Nd and Sm isotopic studies, magma mixing, chemical and mineralogical heterogeneities in basalt source regions, and partial melting controls on basalt chemistry. Attention is also given to features of mare basalts, eucrites, and comparisons of basalts for the earth, the moon, and the parent body of basaltic achondrites.

  12. Nepheline and sodalite in a barred olivine chondrule from the Allende meteorite

    NASA Technical Reports Server (NTRS)

    Lumpkin, G. R.

    1980-01-01

    The discovery of nepheline and sodalite in association with glass in a barred olivine chondrule from the Allende C3V meteorite is reported, and the possible origin of the minerals is discussed. Scanning electron microscope/energy dispersive analysis indicates that the major minerals of the chondrule are olivine, bronzite and chromite, with olivine bars separated by glass of nearly pure plagioclase composition. The olivine is observed to have a composition richer in Fe than that predicted from olivine-liquid equilibria, indicating, along with the presence of plagioclase glass and small amounts of subcalcic diopside, the nonequilibrium crystallization of the barred olivine chondrule. The textural features of the chondrule are consistent with a liquid origin for nepheline and sodalite from the chondrule-forming liquid under nonequilibrium conditions.

  13. High-Mg basalts as a Signal of Magma System Replenishment at Lopevi Island, Vanuatu

    NASA Astrophysics Data System (ADS)

    Stewart, R. B.; Smith, I. E.; Turner, M. B.; Cronin, S. J.

    2007-05-01

    Lopevi is is a basalt to basaltic andesite island stratovolcano in central Vanuatu and is part of a long-lived, mature Island Arc chain. Central Vanuatu is tectonically influenced by the subduction of the D'Entrecasteaux zone. Primitive rock types that have been identified from the arc include picrites, ankaramites and high MgO basalts. High MgO rocks are generally considered to be a relatively rare component of arc-type magma suites but as detailed sequence sampling of individual volcanoes occurs, they have been identified more often. Here we report on the occurrence of high-Mg basalts in a sequence of lavas erupted in the last 100 years from Lopevi volcano. Activity at Lopevi is characteristically intermittent with eruptive sequences occurring over a c. 6 year period, separated by longer periods of repose. A major eruptive episode in 1939 caused evacuation of the island and the next eruptive episode in the 1960's also led to evacuation. The 1960's cycle of activity ended in 1982. The most recent phase of activity commenced in 1998 with a return to eruption of more siliceous, high alumina basaltic andesite. Geochemical data show that the 1960's lavas were different from those erupted earlier and later. They are olivine basalts with up to 9 wt percent MgO, 70 ppm Ni and 300 ppm Cr; Al2O3 content is about 12 wt percent. The 2003 lavas and pre-1960's lavas, in contrast, are basaltic andesites with c. 4 wt percent MgO, less than 25 ppm Ni, less than 100 ppm Cr and c. 20 wt percent Al2O3. The 1960's Lopevi sequence of eruptions represents an injection of a more primitive, high MgO magma at the end of a 21 year quiescent period after the major eruptions of 1939. Injection of small batches of more primitive magmas over decadal time periods at Lopevi marks the initiation of a new magmatic cycle. The occurrence of high MgO magmas as part of a cycle that includes typically low MgO arc type rocks demonstrates a consanguineous relationship and shows that high MgO arc type

  14. Field observations of Flood Basalt structure: Implications for offshore interpretation and sub-volcanic investigation

    NASA Astrophysics Data System (ADS)

    Single, R.; Jerram, D.; Pearson, D.; Hobbs, R.

    2003-04-01

    Field investigations in Skye and Namibia have provided insight into structure and architecture of CFBs. The studies have been developed into lava sequence models in 3-D software GoCad. The understanding has been applied to interpretation of lavas in the Faeroe-Shetland trough. Volcanics hinder petroleum exploration in this play due to their complex internal geometries and velocity structure. Seismic resolution is poor beneath volcanics. Fieldwork has shown that lavas on Skye have developed from (olivine-phyric) compound basalts towards the base of the sequence, into more massive flows higher up the succession. Fieldwork in the Etendeka CFBs reveal a similar style of lava field development. The focus of the offshore study is through the area of the GFA-99 seismic data. Detailed 3-D interpretation over the central data area is 20x20km in dimensions. The lava sequence present may be sub-divided vertically and laterally into 4 zones between the following seismic picks: Base basalt/sub-basalt sills, top compound lava-dominated series, top Middle Series, top hyaloclastites, top massive basalt. Within the lava sequence, the surfaces have rugose topographies. Lower zone lavas are characterised by discontinuous, indistinct reflectors. These are interpreted to be sub-aerially effused basalts with compound-braided architecture. Middle Series basalts are considered to be a combination of compound lavas and more massive, tabular flows. Steeply dipping seismic reflectors also form part of the Middle Series and are interpreted as foreset-bedded hyaloclastites. The uppermost lavas have strong reflection characteristics and are laterally extensive. These are interpreted to be massive tabular lavas covering an area >8.4 x10^3 km^2. Such flows exist in upper parts of CFB sequences as evidenced from fieldwork. Complex stacking arrangements of lavas seen in the field, and the complexities observed in seismic, suggest that many factors need to be considered within CFBs for improved sub

  15. Exogenic olivine on Vesta from Dawn Framing Camera color data

    NASA Astrophysics Data System (ADS)

    Nathues, Andreas; Hoffmann, Martin; Schäfer, Michael; Thangjam, Guneshwar; Le Corre, Lucille; Reddy, Vishnu; Christensen, Ulrich; Mengel, Kurt; Sierks, Holger; Vincent, Jean-Baptist; Cloutis, Edward A.; Russell, Christopher T.; Schäfer, Tanja; Gutierrez-Marques, Pablo; Hall, Ian; Ripken, Joachim; Büttner, Irene

    2015-09-01

    In this paper we present the results of a global survey of olivine-rich lithologies on (4) Vesta. We investigated Dawn Framing Camera (FC) High Altitude Mapping Orbit (HAMO) color cubes (∼60 m/pixel resolution) by using a method described in Thangjam et al. (Thangjam, G., Nathues, A., Mengel, K., Hoffmann, M., Schäfer, M., Reddy, V., Cloutis, E.A., Christensen, U., Sierks, H., Le Corre, L., Vincent, J.-B, Russell, C.T. [2014b]. Meteorit. Planet. Sci. arXiv:1408.4687 [astro-ph.EP]). In total we identified 15 impact craters exhibiting olivine-rich (>40 wt.% ol) outcrops on their inner walls, some showing olivine-rich material also in their ejecta and floors. Olivine-rich sites are concentrated in the Bellicia, Arruntia and Pomponia region on Vesta's northern hemisphere. From our multi-color and stratigraphic analysis, we conclude that most, if not all, of the olivine-rich material identified is of exogenic origin, i.e. remnants of A- or/and S-type projectiles. The olivine-rich lithologies in the north are possibly ejecta of the ∼90 km diameter Albana crater. We cannot draw a final conclusion on their relative stratigraphic succession, but it seems that the dark material (Nathues, A., Hoffmann, M., Cloutis, E.A., Schäfer, M., Reddy, V., Christensen, U., Sierks, H., Thangjam, G.S., Le Corre, L., Mengel, K., Vincent, J.-B., Russell, C.T., Prettyman, T., Schmedemann, N., Kneissl, T., Raymond, C., Gutierrez-Marques, P., Hall, I. Büttner, I. [2014b]. Icarus (239, 222-237)) and the olivine-rich lithologies are of a similar age. The origin of some potential olivine-rich sites in the Rheasilvia basin and at crater Portia are ambiguous, i.e. these are either of endogenic or exogenic origin. However, the small number and size of these sites led us to conclude that olivine-rich mantle material, containing more than 40 wt.% of olivine, is basically absent on the present surface of Vesta. In combination with recent impact models of Veneneia and Rheasilvia (Clenet, H., Jutzi

  16. Helium Diffusion in Olivine

    NASA Astrophysics Data System (ADS)

    Cherniak, D. J.; Watson, E. B.

    2011-12-01

    Diffusion of helium has been characterized in natural Fe-bearing olivine (~Fo90) and synthetic forsterite. Polished, oriented slabs of olivine were implanted with 3He, at 100 keV at a dose of 5x1015/cm2 or at 3.0 MeV at a dose of 1x1016/cm2. A set of experiments on the implanted olivine were run in 1-atm furnaces. In addition to the one-atm experiments, experiments on implanted samples were also run at higher pressures (2.6 and 2.7 GPa) to assess the potential effects of pressure on He diffusion and the applicability of the measured diffusivities in describing He transport in the mantle. The high-pressure experiments were conducted in a piston-cylinder apparatus using an "ultra-soft" pressure cell, with the diffusion sample directly surrounded by AgCl. 3He distributions following experiments were measured with Nuclear Reaction Analysis using the reaction 3He(d,p)4He. This direct profiling method permits us to evaluate anisotropy of diffusion, which cannot be easily assessed using bulk-release methods. For diffusion in forsterite parallel to c we obtain the following Arrhenius relation over the temperatures 250-950°C: D = 3.91x10-6exp(-159 ± 4 kJ mol-1/RT) m2/sec. The data define a single Arrhenius line spanning more than 7 orders of magnitude in D and 700°C in temperature. Diffusion parallel to a appears slightly slower, yielding an activation energy for diffusion of 135 kJ/mol and a pre-exponential factor of 3.73x10-8 m2/sec. Diffusion parallel to b is slower than diffusion parallel to a (by about two-thirds of a log unit); for this orientation an activation energy of 138 kJ/mol and a pre-exponential factor of 1.34x10-8 m2/sec are obtained. This anisotropy is broadly consistent with observations for diffusion of Ni and Fe-Mg in olivine. Diffusion in Fe-bearing olivine (transport parallel to b) agrees within uncertainty with findings for He diffusion in forsterite. The higher-pressure experiments yield diffusivities in agreement with those from the 1-atm

  17. Uranium concentration and distribution in six peridotite inclusions of probable mantle origin

    NASA Technical Reports Server (NTRS)

    Haines, E. L.; Zartman, R. E.

    1973-01-01

    Fission-track activation was used to investigate uranium concentration and distribution in peridotite inclusions in alkali basalt from six localities. Whole-rock uranium concentrations range from 24 to 82 ng/g. Most of the uranium is uniformly distributed in the major silicate phases - olivine, orthopyroxene, and clinopyroxene. Chromian spinels may be classified into two groups on the basis of their uranium content - those which have less than 10 ng/g and those which have 100 to 150 ng/g U. In one sample accessory hydrous phases, phlogopite and hornblende, contain 130 and 300 ng/g U, respectively. The contact between the inclusion and the host basalt is usually quite sharp. Glassy or microcrystalline veinlets found in some samples contain more than 1 microgram/g. Very little uranium is associated with microcrystals of apatite. These results agree with some earlier investigators, who have concluded that suboceanic peridotites contain too little uranium to account for normal oceanic heat flow by conduction alone.

  18. Thermal Emission Spectroscopy of 1 Ceres: Evidence for Olivine

    NASA Technical Reports Server (NTRS)

    Witteborn, F. C.; Roush, T. L.; Cohen, M.

    1999-01-01

    Thermal emission spectra of the largest asteroid 1 Ceres obtained from the Kuiper Airborne Observatory display features that may provide information on its surface mineralogy. A plot of the Ceres spectrum (calibrated using alpha Boo as a standard) divided by a standard thermal model (STM) is shown. Also shown is the emissivity spectrum deduced from reflectivity measurements for olivine grains <5 microns in diameter. The general shape of the Ceres and the olivine curves agree in essential details, such as the maxima from 8 to 12 microns, the minimum between 12 and 14 microns, the broad peak near 17.5 micron, and the slope beyond 22 micron. (Use of the 10 to 15-micron grain reflectivities provides a better match to the 12- to 14-micron dip. We used a value of unity for beta, the beaming factor associated with small-scale surface roughness in our STM. Adjustment of beta to a lower value raises the long-wavelength side of the Ceres spectrum, providing an even better match to the olivine curve.) The emissivity behavior roughly matches the emission coefficients which were calculated for olivine particles with a particle radius of 3 microns. Their calculations show not only the negative slope from 23 to 25 pm, but a continued decrease past 30 micron. The Ceres emissivity is thus similar to that of small olivine grains from 8 to 30 micron, but olivine's emissivity is lower from 5 to 8 pm.

  19. Phosphorus as indicator of magmatic olivine residence time, morphology and growth rate

    NASA Astrophysics Data System (ADS)

    Sobolev, Alexander; Batanova, Valentina

    2015-04-01

    Phosphorus is among of slowest elements by diffusion rate in silicate melts and crystals (e.g. Spandler et al, 2007). In the same time it is moderately incompatible to compatible with olivine (Brunet & Chazot, 2001; Grant & Kohn, 2013). This makes phosphorus valuable tracer of olivine crystallization in natural conditions. Indeed, it is shown that natural magmatic olivine crystals commonly posses strong and complicated zoning in phosphorus (Milman-Barris et al, 2008; Welsch et al, 2014). In this paper we intend to review phosphorus behavior in olivine in published experimental and natural olivine studies and present large set of new EPMA data on phosphorus zoning in olivine phenocrysts from MORBs, OIBs, komatiites and kimberlites. We will show that sharp olivine zones enriched in phosphorus by a factor of 10-20 over prediction by equilibrium partition may be due to formation of P-rich boundary layer on the interface of fast growing olivine. This is proved by finding of small-size (normally 10 mkm or less) exceptionally P-rich melt inclusions in olivine, which are otherwise similar in composition to typical melt. These observations could provide potential olivine growth speedometer. We will also demonstrate, that sharp zoning in phosphorus may provide valuable information on the residence time of olivine crystals in different environments: magma chambers and conduits as well as mantle sources. This study has been founded by Russian Science Foundation grant 14-17-00491. References: Spandler, et al, 2007, Nature, v. 447, p. 303-306; Brunet & Chazot, 2001, Chemical Geology, v. 176, p. 51-72; Grant & Kohn, 2013, American Mineralogist, v. 98, p. 1860-1869; Milman-Barris et al, 2008, Contr. Min. Petrol. v. 155, p.739-765; Welsch et al, 2014, Geology, v. 42, p.867-870.

  20. Magma-Hydrothermal Transition: Basalt Alteration at Supercritical Conditions in Drill Core from Reykjanes, Iceland, Iceland Deep Drilling Project.

    NASA Astrophysics Data System (ADS)

    Zierenberg, R. A.; Fowler, A. P.; Schiffman, P.; Fridleifsson, G. Ó.; Elders, W. A.

    2017-12-01

    The Iceland Deep Drilling Project well IDDP-2, drilled to 4,659 m in the Reykjanes geothermal system, the on-land extension of the Mid Atlantic Ridge, SW Iceland. Drill core was recovered, for the first time, from a seawater-recharged, basalt-hosted hydrothermal system at supercritical conditions. The well has not yet been allowed to heat to in situ conditions, but temperature and pressure of 426º C and 340 bar was measured at 4500 m depth prior to the final coring runs. Spot drill cores were recovered between drilling depths of 3648.00 m and 4657.58 m. Analysis of the core is on-going, but we present the following initial observations. The cored material comes from a basaltic sheeted dike complex in the brittle-ductile transition zone. Felsic (plagiogranite) segregation veins are present in minor amounts in dikes recovered below 4300 m. Most core is pervasively altered to hornblende + plagioclase, but shows only minor changes in major and minor element composition. The deepest samples record the transition from the magmatic regime to the presently active hydrothermal system. Diabase near dike margins has been locally recrystallized to granoblastic-textured orthopyroxene-clinopyroxe-plagioclase hornfels. High temperature hydrothermal alteration includes calcic plagioclase (up to An100) and aluminous hornblende (up to 11 Wt. % Al2O3) locally intergrown with hydrothermal biotite, clinopyroxene, orthopyroxene and/or olivine. Hydrothermal olivine is iron-rich (Mg # 59-64) compared to expected values for igneous olivine. Biotite phenocrysts in felsic segregation veins have higher Cl and Fe compared to hydrothermal biotites. Orthopyroxene-clinopyroxene pairs in partially altered quench dike margins give temperature of 955° to 1067° C. Orthopyroxene-clinopyroxene pairs from hornfels and hydrothermal veins and replacements give temperature ranging from 774° to 888° C. Downhole fluid sampling is planned following thermal equilibration of the drill hole. Previous work

  1. Suitability of chondrules for studying the magnetic field of the early solar system: an examination of synthetically produced dusty olivine

    NASA Astrophysics Data System (ADS)

    Hu, Y.; Feinberg, J. M.; Church, N.; Bromiley, G.; Bowles, J.; Jackson, M.; Moskowitz, B. M.; Harrison, R. J.

    2008-12-01

    Chondritic meteorites are rare, yet incredibly valuable windows into the geophysical and geochemical environment of the early solar system. Dusty olivine grains containing exsolved nanometer-scale iron-nickel alloy inclusions are present in many chondritic meteorites and their remanent magnetization may give insight into the strength of the solar dynamo at the time of chondrule formation. Laboratory methods for determining the paleointensity of these rare materials must be optimized prior to conducting experiments on actual meteorite samples. To this end, we have used high temperature recrystallization techniques to produce synthetic dusty olivine samples with textures remarkably similar to those observed in chondritic meteorites. The olivine grains used in these annealing experiments are from the 13 kya Haleyjabunga picritic basalt flow in Iceland and have compositions of Fo90, which closely resembles the olivine composition observed in chondritic meteorites. Samples were annealed at 1350°C either under vacuum in the presence of graphite or under controlled oxygen fugacity using pure CO gas. The laboratory-produced magnetic mineral assemblages in two sets of samples have been characterized using low and high temperature remanence and susceptibility measurements, hysteresis loops, FORC diagrams, and scanning electron microscopy. The room-temperature remanence properties of these materials have been explored using stepwise IRM and ARM acquisition and alternating field demagnetization. These synthesis techniques allow us to produce a wide rage of iron-nickel grain sizes with correspondingly large variations in coercivity (between 0 and 500 mT). High temperature measurements of saturation magnetization show that both samples reach their Curie temperatures at ~760°C, consistent with kamacite, a low-Ni high-Fe metal alloy. Multiple experiments have shown that care must be taken to rigorously control the atmosphere in which the samples are heated and cooled in order to

  2. Experimentally Determined Subsolidus Metal-Olivine Element Partitioning with Applications to Pallasites.

    PubMed

    Donohue, Patrick H; Hill, Eddy; Huss, Gary R

    2018-02-01

    Pallasite meteorites, which consist primarily of olivine and metal, may be remnants of disrupted core-mantle boundaries of differentiated asteroids or planetesimals. The early thermal histories of pallasites are potentially recorded by minor- and trace-element zonation in olivine. However, constraining this history requires knowledge of element behavior under the conditions of pallasite formation, which is lacking for many of the main elements of interest (e.g., Co, Cr, Mn). In this study, we experimentally determined metal/olivine partition coefficients for Fe, Ni, Co, Cr, and Mn in a pallasite analogue at subsolidus temperatures. Metal/olivine partition coefficients ( K M ) increase in the order K Mn < K Cr < 1 < K Fe < K Co < K Ni , with five orders of magnitude separating K Mn from K Ni . Transition metals also become more siderophile with increasing experimental temperature (900 to 1550°C). The experiments incidentally produced diffusion profiles in olivine for these elements; Our results suggest they diffuse through olivine at similar rates. Core compositions of pallasite olivines are consistent with high-temperature equilibration with FeNi-metal. Olivine zonation toward crystal rims varies significantly for the investigated transition metals. We suggest rim zonation results from partial re-equilibration during late stage crystallization of minor phases (e.g., chromite, phosphates). This re- equilibration occurred over short timescales relative to overall pallasite cooling, likely tied to initial cooling rates on the order of 100-300°C/Myr.

  3. Synthesis of nanometer-sized fayalite and magnesium-iron(II) mixture olivines

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

    Qafoku, Odeta; Ilton, Eugene S.; Bowden, Mark E.

    Olivines are divalent orthosilicates with important geologic, biological, and industrial significance and are typically comprised of mixtures of Mg2+ and Fe2+ ranging from forsterite (Mg2SiO4) to fayalite (Fe2SiO4). Investigating the role of Fe(II) in olivine reactivity requires the ability to synthesize olivines that are nanometer-sized, have different percentages of Mg2+ and Fe2+, and have good bulk and surface purity. This article demonstrates a new method for synthesizing nanosized fayalite and Mg-Fe mixture olivines. First, carbonaceous precursors are generated from sucrose, PVA, colloidal silica, Mg2+, and Fe3+. Second, these precursors are calcined in air to burn carbon and create mixtures ofmore » Fe(III)-oxides, forsterite, and SiO2. Finally, calcination in reducing CO-CO2 gas buffer leads to Fe(II)-rich olivines. XRD, Mössbauer, and IR analyses verify good bulk purity and composition. XPS indicates that surface iron is in its reduced Fe(II) form, and surface Si is consistent with olivine. SEM shows particle sizes predominately between 50 and 450 nm, and BET surface areas are 2.8-4.2 m2/g. STEM HAADF analysis demonstrates even distributions of Mg and Fe among the available M1 and M2 sites of the olivine crystals. These nanosized Fe(II)-rich olivines are suitable for laboratory studies with in situ probes that require mineral samples with high reactivity at short timescales.« less

  4. Experimental research on continuous basalt fiber and basalt-fibers-reinforced polymers

    NASA Astrophysics Data System (ADS)

    Zhang, Xueyi; Zou, Guangping; Shen, Zhiqiang

    2008-11-01

    The interest for continuous basalt fibers and reinforced polymers has recently grown because of its low price and rich natural resource. Basalt fiber was one type of high performance inorganic fibers which were made from natural basalt by the method of melt extraction. This paper discusses basic mechanical properties of basalt fiber. The other work in this paper was to conduct tensile testing of continuous basalt fiber-reinforced polymer rod. Tensile strength and stress-strain curve were obtained in this testing. The strength of rod was fairly equal to rod of E-glass fibers and weaker than rod of carbon fibers. Surface of crack of rod was studied. An investigation of fracture mechanism between matrix and fiber was analyzed by SEM (Scanning electron microscopy) method. A poor adhesion between the matrix and fibers was also shown for composites analyzing SEM photos. The promising tensile properties of the presented basalt fibers composites have shown their great potential as alternative classical composites.

  5. The Use of Basalt, Basalt Fibers and Modified Graphite for Nuclear Waste Repository - 12150

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

    Gulik, V.I.; Biland, A.B.

    2012-07-01

    New materials enhancing the isolation of radioactive waste and spent nuclear fuel are continuously being developed.. Our research suggests that basalt-based materials, including basalt roving chopped basalt fiber strands, basalt composite rebar and materials based on modified graphite, could be used for enhancing radioactive waste isolation during the storage and disposal phases and maintaining it during a significant portion of the post-closure phase. The basalt vitrification process of nuclear waste is a viable alternative to glass vitrification. Basalt roving, chopped basalt fiber strands and basalt composite rebars can significantly increase the strength and safety characteristics of nuclear waste and spentmore » nuclear fuel storages. Materials based on MG are optimal waterproofing materials for nuclear waste containers. (authors)« less

  6. 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.

  7. Crypto-magma chambers beneath Mt. Fuji

    NASA Astrophysics Data System (ADS)

    Kaneko, Takayuki; Yasuda, Atsushi; Fujii, Toshitsugu; Yoshimoto, Mitsuhiro

    2010-06-01

    Mt. Fuji consists dominantly of basalt. A study of olivine-hosted melt-inclusions from layers of air-fall scoria, however, shows clear evidence of andesitic liquids. Whole rock compositions show a narrow range of SiO 2, but a wide range of FeO*/MgO and incompatible elements. Phenocrystic plagioclase generally shows bi-modal distributions in compositional frequency, while most olivine phenocrysts show uni-modal distribution with reverse zoning and often contain andesitic melt-inclusions. These suggest that magmas erupted from Fuji are generated through mixing between basaltic and more SiO 2-rich (often andesitic) end-members. We propose that Fuji's magmatic plumbing system consists of at least two magma chambers: a relatively deep (˜20 km) basaltic one and a relatively shallow (˜ 8-9 km) and more SiO 2-rich one. Evolved basalts with wide compositional ranges of incompatible elements are generated in the deep basaltic magma chamber by prevalent fractional crystallization of pyroxenes with olivine and calcic plagioclase at high pressure. Meanwhile basaltic magma left behind by the previous eruption in the conduit accumulates in a shallow magma chamber, and is differentiated to more SiO 2-rich composition by fractional crystallization of olivine, less-calcic plagioclase, and clinopyroxene. Shortly before a new eruption, a large amount of evolved basaltic magma containing calcic plagioclase rises from the deeper magma chamber and is mixed with the more SiO 2-rich magma in the shallow chamber, to generate the hybrid basaltic magma.

  8. Olivine in Almahata Sitta - Curiouser and Curiouser

    NASA Technical Reports Server (NTRS)

    Zolensky, M. E.; Herrin, J.; Mikouchi, T.; Satake, W.; Kurihara, T.; Sandford, S. A.; Milam, S. N.; Hagiya, K.; Ohsumi, K.; Friedrich, J. M.; hide

    2010-01-01

    Almahata Sitta (hereafter Alma) is an anomalous, polymict ureilite. Anomalous features include low abundance of olivine, large compositional range of silicates, high abundance and large size of pores, crystalline pore wall linings, and overall finegrained texture. Tomography suggests the presence of foliation, which is known from other ureilites. Alma pyroxenes and their interpretation are discussed in two companion abstracts. In this abstract we discuss the composition of olivine in Alma, which is indicative of the complexity of this meteorite.

  9. Minor elements in lunar olivine as a petrologic indicator

    NASA Technical Reports Server (NTRS)

    Steele, I. M.; Smith, J. V.

    1975-01-01

    Accurate electron microprobe analyses (approximately 50 ppm) were made for Al, Ca, Ti, Cr, Mn, and Ni in Mg-rich olivines which may derive from early lunar crust or deeper environments. Low-Ca contents consistently occur only in olivines from dunitic and troctolitic breccia: spinel troctolite and other rock types have high-Ca olivines suggesting derivation by near-surface processes. Rock 15445 has olivine with distinctly low CaO (approximately 0.01 wt.%). Chromium ranges to higher values (max.0.2 oxide wt.%) than for terrestrial harzburgites and lherzolites but is similar to the range in terrestrial komatiites. Divalent chromium may be indicated over trivalent Cr because olivines lack sufficient other elements for charge balance of the latter. NiO values in lunar specimens range from 0.00 to 0.07 wt.% and a weak anticorrelation with Cr2O3 suggests an oxidation state effect. Al2O3 values are mostly below 0.04-wt.% and show no obvious correlation with fragment type. TiO2 values lie below 0.13-wt.% and seem to correlate best with crystallization rate and plagioclase content of the host rock. High values of Al2O3 and TiO2 reported by other workers have not been confirmed, and are probably wrong.

  10. Apollo 15 yellow-brown volcanic glass: Chemistry and petrogenetic relations to green volcanic glass and olivine-normative mare basalts

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

    Hughes, S.S.; Schmitt, R.A.; Oregon State Univ., Corvallis

    1988-10-01

    Apollo 15 yellow-brown glass is one of twenty-five, high Mg, primary magmas emplaced on the lunar surface in pyroclastic eruptions. Forty spherules of this glass were individually analyzed by electron microprobe and INAA for major- and trace-elements. The abundances demonstrate that this primary magma was produced by partial melting of differentiated cumulates in the lunar mantle. Models are developed to explain the possible source-regions of several Apollo 15 and Apollo 12 low-Ti mare magmas as being products of hybridization involving three ancient differentiated components of a primordial lunar magma ocean: (a) early olivine {plus minus} orthopyroxene cumulates; (b) late-stage clinopyroxenemore » + pigeonite + ilmenite + plagioclase cumulates; and (c) late-stage inter-cumulus liquid.« less

  11. Origin of CaCl2 brines by basalt-seawater interaction: Insights provided by some simple mass balance calculations

    NASA Astrophysics Data System (ADS)

    Hardie, Lawrence A.

    1983-06-01

    Modern rift zone hydrothermal brines are typically CaCl2-bearing brines, an unusual chemical signature they share with certain oil field brines, fluid inclusions in ore minerals and a few uncommon saline lakes. Many origins have been suggested for such CaCl2 brines but in the Reykjanes, Iceland, geothermal system a strong empirical case can be made for a basalt-seawater interaction origin. To examine this mechanism of CaCl2 brine evolution some simple mass balance calculations were carried out. Average Reykjanes olivine tholeiite was “reacted” with average North Atlantic seawater to make an albite-chlorite-epidotesphene rock using Al2O3 as the conservative rock component and Cl as the conservative fluid component. The excess components released by the basalt to the fluid were “precipitated” at 275° C as quartz, calcite, anhydrite, magnetite and pyrite to complete the conversion to greenstone. The resulting fluid was a CaCl2 brine of seawater chlorinity with a composition remarkably similar to the actual Reykjanes brine at 1750 m depth. Thus, the calculations strongly support the idea that the Reykjanes CaCl2 brines result from “closed system” oceanic basalt-seawater interaction (albitization — chloritization mechanism) at greenschist facies temperatures. The calculation gives a seawater: basalt mass ratio of 3∶1 to 4∶1 (vol. ratio of 9∶1 to 12∶1), in keeping with experimental results, submarine vent data and with ocean crust cooling calculations. The brine becomes anoxic because there is insufficient dissolved or combined oxygen to balance all the Fe released from the basalt during alteration. Large excesses of Ca are released to the fluid and precipitate out in the form of anhydrite which essentially sweeps the brine free of sulfate leaving an elevated Ca concentration. The calculated rock-water interaction basically involves Na + Mg + SO4 ⇌ Ca + K, simulating chemical differences observed between oceanic basalts and greenstones from many

  12. Association of Sub-continental and Asthenosphere related Volcanism in NW Iran,Implication forMantle thermal perturbation induced by slab break off and collision event

    NASA Astrophysics Data System (ADS)

    Jahangiri, A.

    2017-12-01

    Cenozoic magmatic rocks occur extensively in the north of the Zagros suture zone and constitute a significant component of the continental crust in this segment of the Alpine-Himalayan orogenic belt. They range in age from Eocene to quaternary. Miocene to Plio-Quaternary volcanism with post-collisional related significant is covered vast areas in NW Iran. These volcanic rocks can be divided into three different sub-groups on the basis of their mineralogy, geochemistry and magma sources including: 1. alkaline leucite-bearing mafic rocks, which are characterized with high ratios of K2O/Na2O, high content LILE and low HFS elements like Ti, Nb and Ta. They are display fractionated REE patterns and based on different discrimination diagrams show similarity with subduction related magmas. 2- Olivine basalt to trachy-basaltic samples which shows similarity to within plate basalts with high content of TiO2, Nb, Ta and fractionated REE pattern. However, compared with a global average of OIB, they are display slightly higher LIL elements and lower HFS elements concentrations, features that resemble to the arc magmas and suggest that the source of the magmas may have been contaminated by slab-derived fluids. These rocks have simple mineralogical composition with plagioclase, clinopyroxene and olivine. 3- Dominant dacitic volcanic rocks with adakitic geochemical characteristics such as highly fractionate REE pattern and high Sr/Y ratio. Generation of adakitic magmas can be related to increased temperatures in the subduction zone due to mantle upwelling and slab tearing. Subsequent asthenospheric upwelling could be caused direct melting of sub-continental mantle to produce the alkaline magmas, with high contents of K2O, MgO and volatile rich phase's potassic magmas that led to crystallization of leucite, phlogopite, apatite and olivine in studied samples. Rupture of the continental lithosphere by strike-slip-related transtensional deformation might have caused decompression

  13. Alkali silica reaction (ASR) in cement free alkali activated sustainable concrete.

    DOT National Transportation Integrated Search

    2016-12-19

    This report summarizes the findings of an experimental evaluation into alkali silica : reaction (ASR) in cement free alkali-activated slag and fly ash binder concrete. The : susceptibility of alkali-activated fly ash and slag concrete binders to dele...

  14. Process to separate alkali metal salts from alkali metal reacted hydrocarbons

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

    Gordon, John Howard; Alvare, Javier; Larsen, Dennis

    A process to facilitate gravimetric separation of alkali metal salts, such as alkali metal sulfides and polysulfides, from alkali metal reacted hydrocarbons. The disclosed process is part of a method of upgrading a hydrocarbon feedstock by removing heteroatoms and/or one or more heavy metals from the hydrocarbon feedstock composition. This method reacts the oil feedstock with an alkali metal and an upgradant hydrocarbon. The alkali metal reacts with a portion of the heteroatoms and/or one or more heavy metals to form an inorganic phase containing alkali metal salts and reduced heavy metals, and an upgraded hydrocarbon feedstock. The inorganic phasemore » may be gravimetrically separated from the upgraded hydrocarbon feedstock after mixing at a temperature between about 350.degree. C. to 400.degree. C. for a time period between about 15 minutes and 2 hours.« less

  15. 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).

  16. Petrology of gabbroic xenoliths in 1960 Kilauea basalt: crystalline remnants of prior (1955) magmatism

    USGS Publications Warehouse

    Fodor, R.V.; Moore, R.B.

    1994-01-01

    The 1960 Kapoho lavas of Kilauea's east rift zone contain 1-10 cm xenoliths of olivine gabbro, olivine gabbro-norite, and gabbro norite. Textures are poikilitic (ol+sp+cpx in pl) and intergranular (cpx+pl??ol??opx). Poikilitic xenoliths, which we interpret as cumulates, have the most primitive mineral compositions, Fo82.5, cpx Mg# 86.5, and An80.5. Many granular xenoliths (ol and noritic gabbro) contain abundant vesicular glass that gives them intersertal, hyaloophitic, and overall 'open' textures to suggest that they represent 'mush' and 'crust' of a magma crystallization environment. Their phase compositions are more evolved (Fo80-70, cpx Mg# 82-75, and An73-63) than those of the poikilitic xenoliths. Associated glass is basaltic, but evolved (MgO 5 wt%; TiO2 3.7-5.8 wt%). The gabbroic xenolith mineral compositions fit existing fractional crystallization models that relate the origins of various Kilauea lavas to one another. FeO/MgO crystal-liquid partitioning is consistent with the poikilitic ol-gabbro assemblage forming as a crystallization product from Kilauea summit magma with ???8 wt% MgO that was parental to evolved lavas on the east rift zone. For example, least squares calculations link summit magmas to early 1955 rift-zone lavas (???5 wt% MgO) through ???28-34% crystallization of the ol+sp+cpx+pl that comprise the poikilitic ol-gabbros. The other ol-gabbro assemblages and the olivine gabbro-norite assemblages crystallized from evolved liquids, such as represented by the early 1955 and late 1955 lavas (???6.5 wt% MgO) of the east rift zone. The eruption of 1960 Kapoho magmas, then, scoured the rift-zone reservoir system to entrain portions of cumulate and solidification zones that had coated reservoir margins during crystallization of prior east rift-zone magmas. ?? 1994 Springer-Verlag.

  17. Distribution of differentiated tholeiitic basalts on the lower east rift zone of Kilauea Volcano, Hawaii: a possible guide to geothermal exploration.

    USGS Publications Warehouse

    Moore, R.B.

    1983-01-01

    Geological mapping of the lower east rift zone indicates that >100 eruptions have extruded an estimated 10 km3 of basalt during the past 2000 yr; six eruptions in the past 200 yr have extruded approx 1 km3. The eruptive recurrence interval has ranged 1-115 yr since the middle of the 18th century and has averaged 20 yr or less over the past 2000 yr. New chemical analyses (100) indicate that the tholeiites erupted commonly differentiated beyond olivine control or are hybrid mixtures of differentiates with more mafic (olivine-controlled) summit magmas. The distribution of vents for differentiated lavas suggests that several large magma chambers underlie the lower east rift zone. Several workers have recognized that a chamber underlies the area near a producing geothermal well, HGP-A; petrological and 14C data indicate that it has existed for at least 1300 yr. Stratigraphy, petrology and surface-deformation patterns suggest that two other areas, Heiheiahulu and Kaliu, also overlie magma chambers and show favourable geothermal prospects.-A.P.

  18. Water in Pyroxene and Olivine from Martian Meteorites

    NASA Technical Reports Server (NTRS)

    Peslier, A. H.

    2012-01-01

    Water in the interior of terrestrial planets can be dissolved in fluids or melts and hydrous phases, but can also be locked as protons attached to structural oxygen in lattice defects in nominally anhydrous minerals (NAM) like olivine, pyroxene, or feldspar [1-3]. Although these minerals contain only tens to hundreds of ppm H2O, this water can amount to at least one ocean in mass when added at planetary scales because of the modal dominance of NAM in the mantle and crust [4]. Moreover these trace amounts of water can have drastic effects on melting temperature, rheology, electrical and heat conductivity, and seismic wave attenuation [5]. There is presently a debate on how much water is present in the martian mantle. Secondary ionization mass spectrometry (SIMS) studies of NAM [6], amphiboles and glass in melt inclusions [7-10], and apatites [11, 12] from Martian meteorites report finding as much water as in the same phases from Earth's igneous rocks. Most martian hydrous minerals, however, generally have the relevant sites filled with Cl and F instead of H [13, 14], and experiments using Cl [15] in parent melts can reproduce Martian basalt compositions as well as those with water [16]. We are in the process of analyzing Martian meteorite minerals by Fourier transform infrared spectrometry (FTIR) in order to constrain the role of water in this planet s formation and magmatic evolution

  19. Trace Element Compositions of Pallasite Olivine Grains and Pallasite Origin

    NASA Technical Reports Server (NTRS)

    Mittlefehldt, David W.; Herrin, J. S.

    2010-01-01

    Pallasites are mixtures of metal with magnesian olivine. Most have similar metal compositions and olivine oxygen isotopic compositions; these are the main-group pallasites (PMG). The Eagle Station grouplet of pallasites (PES) have distinctive metal and olivine compositions and oxygen isotopic compositions. Pallasites are thought to have formed at the core-mantle boundary of their parent asteroids by mixing molten metal with solid olivine of either cumulatic or restitic origin. We have continued our investigation of pallasite olivines by doing in situ trace element analyses in order to further constrain their origin. We determined Al, P, Ca, Ga and first row transition element contents of olivine grains from suite of PMG and PES by LA-ICP-MS at JSC. Included in the PMG suite are some that have anomalous metal compositions (PMG-am) and atypically ferroan olivines (PMG-as). Our EMPA work has shown that there are unanticipated variations in olivine Fe/Mn, even within those PMG that have uni-form Fe/Mg. Manganese is homologous with Fe2+, and thus can be used the same way to investigate magmatic fractionation processes. It has an advantage for pallasite studies in that it is unaffected by redox exchange with the metal. PMG can be divided into three clusters on the basis of Mn/Mg; low, medium and high that can be thought of as less, typically and more fractionated in an igneous sense. The majority of PMG have medium Mn/Mg ratios. PMG-am occur in all three clusters; there does not seem to be any relationship between putative olivine igneous fractionation and metal composition. The PMG-as and one PMG-am make up the high Mn/Mg cluster; no PMG are in this cluster. The high Mn/Mg cluster ought to be the most fractionated (equivalent to the most Fe-rich in igneous suites), yet they have among the lowest contents of incompatible lithophile elements Al and Ti and the two PMG-as in this cluster also have low Ca and Sc contents. This is inconsistent with simple igneous

  20. Precious metal enrichment at low-redox in terrestrial native Fe-bearing basalts investigated using laser-ablation ICP-MS

    NASA Astrophysics Data System (ADS)

    Howarth, Geoffrey H.; Day, James M. D.; Pernet-Fisher, John F.; Goodrich, Cyrena A.; Pearson, D. Graham; Luo, Yan; Ryabov, Viktor V.; Taylor, Lawrence A.

    2017-04-01

    Primary native Fe is a rare crystallizing phase from terrestrial basaltic magmas, requiring highly reducing conditions (fO2 basaltic magmas can be achieved through assimilation of carbonaceous crustal material, which leads to formation of an immiscible, molten, C-rich, native Fe alloy liquid. If this liquid also contains sufficient sulfur, it can undergo further division into conjugate Fe-C-rich and a Fe-S-rich immiscible melts that can effectively scavenge the highly siderophile elements (HSE: Re, Au, and the platinum group elements [PGE], Pd, Pt, Rh, Ru, Ir, Os), as well as Ni and Cu, to economic abundances. Three localities are known globally where native Fe bearing mafic rocks occur: (1) Paleocene basalts of Disko Island, West Greenland; (2) a Miocene lava of the Bühl basalts, Germany; and (3) mafic intrusions associated with the Late Permian Siberian flood basalts. In this contribution, we report major- and minor-element compositions and HSE concentrations for the main alloy phases (FeNi metal and cohenite) and sulfide, for all three known global occurrences of native Fe bearing basalt. Total HSE abundances in metal grains, obtained by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), are lowest in the Bühl basalt, (∼0.05 ppm), intermediate in the Disko Island basalts (4-8 ppm), and highest the Siberian Khungtukun and Dzhaltul intrusions (10-30 ppm). These differences demonstrate that, while native Fe formation is the result of carbonaceous crustal assimilation, HSE enrichment is not ubiquitous during this process. The Siberian occurrences are characterized by Pt PGE (PPGE: Pt, Pd) enrichment relative to the Ir PGE (IPGE: Rh, Ru, Ir, Os), consistent with models of early stage fractionation of olivine, chromite and metallic IPGE in staging magma reservoirs, prior to the addition of C-rich crustal materials in the shallow crust. Relative to Noril'sk Ni-Cu-PGE sulfide ores

  1. 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

  2. Alkali metal nitrate purification

    DOEpatents

    Fiorucci, Louis C.; Morgan, Michael J.

    1986-02-04

    A process is disclosed for removing contaminants from impure alkali metal nitrates containing them. The process comprises heating the impure alkali metal nitrates in solution form or molten form at a temperature and for a time sufficient to effect precipitation of solid impurities and separating the solid impurities from the resulting purified alkali metal nitrates. The resulting purified alkali metal nitrates in solution form may be heated to evaporate water therefrom to produce purified molten alkali metal nitrates suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of purified alkali metal nitrates.

  3. High pressure breakdown of antigorite to spinifex-textured olivine and orthopyroxene, SE Spain

    NASA Astrophysics Data System (ADS)

    Trommsdorff, V.; Sánchez-Vizcaíno, V. López; Gómez-Pugnaire, M. T.; Müntener, O.

    The prograde, high pressure, transition from antigorite serpentinite to enstatite-olivine rock occurs along a tectonically undisturbed profile at Cerro del Almirez, SE Spain. The reactant assemblage is antigorite + olivine with tremolite rimming precursor diopside. The product assemblage of tremolite + chlorite + enstatite + olivine has a spinifex-like texture with arborescent or radiating olivine elongated parallel to [001] and with radially grown enstatite. Product enstatite is very poor in Al2O3. Due to numerous oriented submicroscopic inclusions of chromian magnetite, product olivine has a brownish pleochroism and a bulk chromium content similar to precursor antigorite. Titanian clinohumite with a fluorine content of 0.45-0.50 wt% persisted beyond the breakdown of antigorite. The partitioning of iron and magnesium amongst the silicate phases is almost identical to that at lower pressures. Average Kd values Mn/Mg and Ni/Mg are 0.17 and 0.70 for antigorite-olivine pairs and 1.83 and 0.22 for orthopyroxene-olivine pairs, respectively. These data are useful in discriminating generations of olivine grown on each other. From the field data a phase diagram topology for a portion of the system CaO-MgO-SiO2-H2O is derived. This topology forms the basis for extrapolations into inaccessible P-T regions.

  4. Are high 3He/4He ratios in oceanic basalts an indicator of deep-mantle plume components?

    USGS Publications Warehouse

    Meibom, A.; Anderson, D.L.; Sleep, Norman H.; Frei, R.; Chamberlain, C.P.; Hren, M.T.; Wooden, J.L.

    2003-01-01

    The existence of a primordial, undegassed lower mantle reservoir characterized by high concentration of 3He and high 3He/4He ratios is a cornerstone assumption in modern geochemistry. It has become standard practice to interpret high 3He/4He ratios in oceanic basalts as a signature of deep-rooted plumes. The unfiltered He isotope data set for oceanic spreading centers displays a wide, nearly Gaussian, distribution qualitatively similar to the Os isotope (187Os/188 Os) distribution of mantle-derived Os-rich alloys. We propose that both distributions are produced by shallow mantle processes involving mixing between different proportions of recycled, variably aged radiogenic and unradiogenic domains under varying degrees of partial melting. In the case of the Re-Os isotopic system, radiogenic mid-ocean ridge basalt (MORB)-rich and unradiogenic (depleted mantle residue) endmembers are constantly produced during partial melting events. In the case of the (U+Th)-He isotope system, effective capture of He-rich bubbles during growth of phenocryst olivine in crystallizing magma chambers provides one mechanism for 'freezing in' unradiogenic (i.e. high 3He/4He) He isotope ratios, while the higher than chondritic (U+Th)/He elemental ratio in the evolving and partially degassed MORB melt provides the radiogenic (i.e. low 3He/4He) endmember. If this scenario is correct, the use of He isotopic signatures as a fingerprint of plume components in oceanic basalts is not justified. Published by Elsevier Science B.V.

  5. Water Retention and Rheology of Ti-doped, Synthetic Olivine

    NASA Astrophysics Data System (ADS)

    Faul, U.; Jackson, I.; Fitz Gerald, J. D.

    2012-12-01

    Upper mantle flow laws are currently based almost entirely on experiments with olivine from San Carlos in Arizona. Synthetically produced olivine enables the exploration of the effects of trace elements on the rheology. We have conducted a range of experiments in a gas medium apparatus with solution-gelation derived olivine that show that titanium is the most effective in binding water in the olivine structure. The FTIR signature of this structurally bound water is most similar to that of water-undersaturated natural olivine with absorption bands at 3575 and 3525 cm-1. Water added, titanium-free solgel contains little water after hotpressing and shows adsorption bands at wavenumbers near 3200 cm-1. Noble metal capsules such as Pt or AuPd, providing more oxidizing conditions, are more effective in retaining water. Experiments with NiFe-lined welded Pt capsules retain no more water than NiFe lined samples without Pt capsule. Water retention is, however, again dependent on trace element content, with Ti doped samples containing tens of ppm after hotpressing. By comparison undoped samples run under the same conditions contain little water, again with different FTIR spectra to Ti-doped samples. Our experiments suggest that Ti by itself, or with water contents at the FTIR detection limit enhances diffusion creep rates relative to undoped, dry solgel olivine. Water contents around 10 ppm in NiFe wrapped samples show an enhancement of strain rates of more than one order of magnitude. The addition of Ti, together with the presence of water, also enhances grain growth. For more coarse-grained samples in the dislocation creep regime the enhancement of the stain rate as a function of water content is approximately consistent with the flow laws of Hirth and Kohlstedt (2003).

  6. Fe(II) Oxidation and Sources of Acidity on Mars

    NASA Technical Reports Server (NTRS)

    Niles, P. B.; Peretyazkho, T. S.; Sutter, B.

    2017-01-01

    There is an apparent paradox be-tween the evidence that aqueous environments on Mars were predominantly acidic, and the fact that Mars is predominantly a basaltic (and olivine-rich) planet. The problem being that basalt and olivine will act to neutralize acidic solutions they come into contact with, and that there is a lot more basaltic crust on Mars than water or acid. This is especially true if there is an appreciable amount of water available to bring the acid in contact with the basaltic crust. Several hypotheses for ancient mar-tian environments call on long lived groundwater and aqueous systems.

  7. Geochemistry of Pallasite Olivines and the Origin of Main-Group Pallasites

    NASA Technical Reports Server (NTRS)

    Mittlefehldt, D. W.; Rumble, D., III

    2006-01-01

    Main-group pallasites (PMG) are mixtures of iron-nickel metal and magnesian olivine thought to have been formed at the core-mantle boundary of an asteroid [1]. Some have anomalous metal compositions (PMG-am) and a few have atypically ferroan olivines (PMG-as) [2]. PMG metal is consistent with an origin as a late fractionate of the IIIAB iron core [2]. Most PMG olivines have very similar Fe/Mg ratios, likely due to subsolidus redox reaction with the metal [3]. In contrast, minor and trace elements show substantial variation, which may be explained by either: (i) PMG were formed at a range of depths in the parent asteroid; the element variations reflect variations in igneous evolution with depth, (ii) the pallasite parent asteroid was chemically heterogeneous; the heterogeneity partially survived igneous processing, or (iii) PMG represent the core-mantle boundaries of several distinct parent asteroids [4, 5]. We have continued doing major, minor and trace elements by EMPA and INAA on a wider suite of PMG olivines, and have begun doing precise oxygen isotope analyses to test these hypotheses. Manganese is homologous with Fe(2+), and can be used to distinguish between magmatic and redox processes as causes for Fe/Mg variations. PMG olivines have a range in molar 1000*Mn/Mg of 2.3-4.6 indicating substantial igneous fractionation in olivines with very similar Fe/Mg (0.138-0.148). The Mg-Mn-Fe distributions can be explained by a fractional crystallization-reduction model; higher Mn/Mg ratios reflect more evolved olivines while Fe/Mg is buffered by redox reactions with the metal. There is a positive association between Mn/Mg and Sc content that is consistent with igneous fractionation. However, most PMG olivines fall within a narrow Mn/Mg range (3.0-3.6), but these show a substantial range in Sc (1.00-2.29 micro-g/g). Assuming fractional crystallization, this Sc range could have resulted from approx.65% crystallization of an ultramafic magma. This is inconsistent with

  8. A Calcium-in-Olivine Geohygrometer and its Application to Subduction Zone Magmatism

    NASA Astrophysics Data System (ADS)

    Gavrilenko, M.; Herzberg, C. T.; Vidito, C. A.; Carr, M. J.; Tenner, T.; Ozerov, A.

    2016-12-01

    Calcium contents of subduction zone olivines are lower than those for olivines from modern MORB, Archean komatiites, and Hawaii (Fig. 1). A role for magmatic H2O is likely for subduction zone olivines, and we have explored the suggestion by [1] that H2O has affected the partitioning of CaO between olivine and silicate melt. We provide a provisional calibration of DCaOOl/L as a function of magmatic MgO and H2O, based on nominally anhydrous experiments (Fig. 2) and minimally degassed H2O contents of olivine-hosted melt inclusions (Fig. 3). The low diffusivity of Ca in olivine [2], when compared to that of H+ [3, 4, 5, 6], might help to retain the memory of magmatic water that is otherwise lost by diffusion and degassing. Application of our geohygrometer (Fig. 4) typically yields 3 to 4 wt. % magmatic H2O at the Kamchatka and Central American arcs for olivines having 1000 ppm Ca, which agrees with H2O maxima from melt inclusion studies [7]; Cerro Negro and Shiveluch volcanoes are exceptions, with about 6% H2O. Our geohygrometer is by no means a replacement for more accurate methods of H2O analysis, but it has the advantage of applicability in cases where olivine-hosted melt inclusions do not exist (or in case when melt inclusions are partly or completely degassed). Additionally, application of the geohygrometer to core-rim olivine Ca analyses has the potential to reveal changes in magmatic H2O, as revealed by Klyuchevskoy and Shiveluch volcanoes. High precision EMPA analyses with 10-20 µm spatial resolution on some olivine grains from Klyuchevskoy and Shiveluch show a decrease in Ca content from core centers to the rim contacts. Our geohygrometer indicates the olivine grains may record changing magmatic H2O. Furthermore, high Mg numbers and Ni contents indicate these are mantle olivines, and the inferred H2O may be recording entry from the slab to the mantle wedge, a prediction that will be tested by SIMS analyses. References: [1] Feig et al. (2006) CMP, 152

  9. The storage capacity of fluorine in olivine and pyroxene under upper mantle conditions

    NASA Astrophysics Data System (ADS)

    Grützner, Tobias; Kohn, Simon C.; Bromiley, David W.; Rohrbach, Arno; Berndt, Jasper; Klemme, Stephan

    2017-07-01

    We present new experimental results on the fluorine storage capacity of olivine and orthopyroxene in the Earth's mantle. Experiments were performed in the system MgO-SiO2 + MgF2 at temperatures between 1350 °C and 1700 °C and pressures up to 17 GPa. Electron microprobe measurements show that fluorine concentrations in olivine reach up to 5100 μg/g. The storage capacity of fluorine in olivine shows only a small pressure dependence but a strong temperature dependence with a positive correlation between increasing temperature and fluorine storage capacity. Fluorine concentrations found in enstatite are one order of magnitude smaller and reach up to 670 μg/g. Our data show that concentrations of fluorine in fluorine-saturated olivine are in the same range as water concentrations in olivine. Nevertheless, fluorine and water solubility in olivine show opposing behavior with increasing pressure and temperature. The fluorine solubility in olivine increases with increasing temperature but is not much affected by pressure. In contrast, water solubility in olivine has previously been shown to decrease with increasing temperature and increase with increasing pressure. Our experiments show that nominally fluorine-free minerals like forsterite and enstatite are capable of storing the entire fluorine budget of the upper mantle, without the need to invoke accessory phases such as apatite or amphibole.

  10. 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.

  11. Ultramafic lavas and high-Mg basaltic dykes from the Othris ophiolite complex, Greece

    NASA Astrophysics Data System (ADS)

    Baziotis, Ioannis; Economou-Eliopoulos, Maria; Asimow, Paul D.

    2017-09-01

    We evaluate the petrography and geochemistry of an unusual suite of subduction-related Phanerozoic high-MgO rocks from the Othris ophiolite complex in Greece, some of which have previously been described as komatiitic lavas. In particular, we study ultramafic, olivine-phyric lavas from the Agrilia area and high-Mg basaltic dykes from the Pournari area. We seek to define primary magmatic MgO contents and initial liquidus temperatures as well as the differentiation sequence and cooling rates experienced by the lavas and dykes. One of our goals is to relate the Othris case to known komatiite and boninite occurrences and to address whether Othris documents an important new constraint on the temporal evolution of ambient mantle temperature, plume-related magmatism, and subduction of oceanic lithosphere. We conclude that, despite whole-rock MgO contents of 31-33 wt%, the olivine-phyric lavas at Agrilia had an upper limit liquid MgO content of 17 wt% and are therefore picrites, not komatiites. The Agrilia lavas contain the unusual Ti-rich pyroxenoid rhönite; we discuss the significance of this occurrence. In the case of the Pournari high-Mg dykes, the distinctive dendritic or plumose clinopyroxene texture, though it resembles in some ways the classic spinifex texture of komatiites, is simply evidence of rapid cooling at the dyke margin and not evidence of extraordinarily high liquidus temperatures. We correlate the dendritic texture with disequilibrium mineral chemistry in clinopyroxene to constrain the cooling rate of the dyke margins.

  12. Petrological characterization of the seismic low-velocity anomaly beneath the Eifel volcanic field (West Germany) using major and trace element compositions of olivine macrocrysts

    NASA Astrophysics Data System (ADS)

    Dejan, Prelevic; Dieter, Mertz; Regina, Mertz-Kraus; Stephan, Buhre

    2014-05-01

    The Eifel volcanic field is part of the Central European Cenozoic Magmatic Province and was periodically active from the mid-Cretaceous until the latest Pleistocene. Two contrasting models are used to explain sources and magma generation mechanisms of the Pleistocene Eifel volcanism: i) decompressional partial melting at the base of the subcontinental lithosphere as a consequence of extension caused by lithospheric flexuring from emplacement of Alpine nappes (Wilson & Downes, 1991); ii) plume-type thermal upwelling in the asthenosphere on the basis of seismic tomography indicating a low-velocity anomaly beneath the Eifel probably caused by temperatures higher than the normal asthenosphere adiabat (e.g., Ritter et al. 2001). We present high-precision electron microprobe data for major and minor elements as well as laser ablation ICP-MS data for trace elements of olivine from the Eifel in order to put new constraints on the origin of Pleistocene Eifel volcanism. Being an early liquidus phase in the crystallization of basaltic melts, olivine composition may be used to characterize the composition of primary mantle melts and their source region in terms of major and trace elements. Moreover, it is useful for T estimation providing a snapshot of the liquid equilibria at early magmatic stage. In addition, important petrological parameters can be constrained, like the extent of prior melt extraction of their mantle source, the presence of different geochemical components in the source, olivine residence times etc. Olivine macrocrysts occur in most of the Eifel Mg-rich lavas, forming up to 10 vol% of the rocks. We studied olivines from 10 representative lava flows of basanitic composition. Based on compositional and textural differences, three genetic groups are recognized: i) volumetrically dominant igneous olivines or phenocrysts (melt related); they are equilibrated with their host melt showing normal zonation (core-rim Fo89-80) and NiO contents up to 0.3 wt%, whereas

  13. Martian dunite NWA 2737: Integrated spectroscopic analyses of brown olivine

    NASA Astrophysics Data System (ADS)

    Pieters, Carle M.; Klima, Rachel L.; Hiroi, Takahiro; Dyar, M. Darby; Lane, Melissa D.; Treiman, Allan H.; Noble, Sarah K.; Sunshine, Jessica M.; Bishop, Janice L.

    2008-06-01

    A second Martian meteorite has been identified that is composed primarily of heavily shocked dunite, Northwest Africa (NWA) 2737. This meteorite has several similarities to the Chassigny dunite cumulate, but the olivine is more Mg rich and, most notably, is very dark and visually brown. Carefully coordinated analyses of NWA 2737 whole-rock and olivine separates were undertaken using visible and near-infrared reflectance, midinfrared emission and reflectance, and Mössbauer spectroscopic studies of the same samples along with detailed petrography, chemistry, scanning electron microscopy, and transmission electron microscopy analyses. Midinfrared spectra of this sample indicate that the olivine is fully crystalline and that its molecular structure remains intact. The unusual color and spectral properties that extend from the visible through the near-infrared part of the spectrum are shown to be due to nanophase metallic iron particles dispersed throughout the olivine during a major shock event on Mars. Although a minor amount of Fe3+ is present, it cannot account for the well-documented unusual optical properties of Martian meteorite NWA 2737. Perhaps unique to the Martian environment, this ``brown'' olivine exhibits spectral properties that can potentially be used to remotely explore the pressure-temperature history of surface geology as well as assess surface composition.

  14. Deformation of olivine during phase transformation to wadsleyite

    NASA Astrophysics Data System (ADS)

    Mohiuddin, A.; Girard, J.; Karato, S. I.

    2017-12-01

    The strength of subducting slabs in the transition zone is critical in controlling the style of mantle convection. However, rheological properties of a subducted slab are elusive: low temperatures of a slab would make slabs strong, but in many regions there is evidence of intense deformation of slabs in the transition zone. One potential cause of intense deformation of subducting slabs is grain size reduction and accompanied microstructural changes during phase transformation of olivine to its higher-pressure polymorphs. There have been no experimental studies to quantify the influence of grain-size evolution. In addition to grain size reduction, distribution of small grains during phase transformation governs the degree of weakening during phase transformation (for e.g. load bearing framework vs. inter-connected layered framework). We conducted laboratory studies on the size and spatial distribution of new grains of wadsleyite after the transformation from olivine. Our results under static conditions show that an interconnected microstructure develops during the initial stage of phase transformation and that the grain size of the interconnected phase (wadsleyite) depends on the temperature at which the phase transformation occurs (smaller grains at lower temperatures). Development of an interconnected microstructure may lead to strain localization in the weaker phase, i.e. the fine-grained interconnected network accommodates most of the strain and therefore weakening of the entire composite. We will test this model through a series of two synchrotron in-situ deformation experiments: (i) Olivine aggregate will be deformed during slow pressure increase from deep upper mantle pressure ( 10 GPa) to transition zone pressure ( 15 GPa) at a given temperature simulating the deformation of a slab penetrating into the transition zone (ii) olivine is partially transformed to wadsleyite in a multi anvil apparatus at Yale and will be deformed within the stability field where

  15. Dehydration Rate of Olivines with Application to Magma Ascent Rate

    NASA Astrophysics Data System (ADS)

    Plank, T. A.; Ferriss, E.; Walker, D.; Newcombe, M. E.

    2017-12-01

    The physics of magma transport and eruption are highly sensitive to the decompression rate, for which few measurements exist. There is great promise, however, in being able to use olivine dehydration to clock the ascent of magmas and xenoliths prior to eruption. Every olivine phenocryst we have measured is zoned in water (H) as a consequence of decompression-driven-degassing and diffusion through the olivine. A major impediment to exploiting this crystal clock, however, is the appropriate diffusivity to use. Published laboratory measurements vary by > 5 orders of magnitude. In order to better define the dehydration rates operating in natural olivines, we conducted laboratory experiments using the whole-block method [1], which allows a finely-resolved time series of H profiles in 3 crystallographic directions using the same sample for all dehydration steps. Starting materials consisted of an untreated olivine from the 1959 Kilauea Iki eruption, and a San Carlos olivine first hydrated in a piston cylinder at NNO, 800°C and 1 GPa for 17.5 hours, just enough to saturate the proton-polaron (p-p) mechanism [2]. Samples were dehydrated at 1 atm, NNO-2.6 and 1000 and 800°C in 6-7 time steps over 8-68 total hours. Both samples show rapid movement of different FTIR absorption bands during the first few hours at 800°C, at the p-p rate. Water loss then converges to a rate intermediate between p-p and proton-Mg-vacancy (p-v) rates for both crystals. In San Carlos, water loss from the 3600 cm-1 band (Si-vacancy defect) speeds up after 20 hours, while the 3525 cm-1 band (Ti-clinohumite defect) slows down, until both are dehydroxylating at a rate of 20% p-p:80% p-v. The apparent diffusivity of these bands is > 4 orders of magnitude faster than the same bands in synthetic forsterite [3]. The Iki olivine dehydrates at a constant rate from 3-8 hrs at 1000°C, at 12% p-p: 88% p-v. Both crystals show very similar diffusivity along [100] at 1000°C (logD -10.5 m2/s). This study thus

  16. Phreatic explosions during basaltic fissure eruptions: Kings Bowl lava field, Snake River Plain, USA

    NASA Astrophysics Data System (ADS)

    Hughes, Scott S.; Kobs Nawotniak, Shannon E.; Sears, Derek W. G.; Borg, Christian; Garry, William Brent; Christiansen, Eric H.; Haberle, Christopher W.; Lim, Darlene S. S.; Heldmann, Jennifer L.

    2018-02-01

    Physical and compositional measurements are made at the 7 km-long ( 2200 years B.P.) Kings Bowl basaltic fissure system and surrounding lava field in order to further understand the interaction of fissure-fed lavas with phreatic explosive events. These assessments are intended to elucidate the cause and potential for hazards associated with phreatic phases that occur during basaltic fissure eruptions. In the present paper we focus on a general understanding of the geological history of the site. We utilize geospatial analysis of lava surfaces, lithologic and geochemical signatures of lava flows and explosively ejected blocks, and surveys via ground observation and remote sensing. Lithologic and geochemical signatures readily distinguish between Kings Bowl and underlying pre-Kings Bowl lava flows, both of which comprise phreatic ejecta from the Kings Bowl fissure. These basalt types, as well as neighboring lava flows from the contemporaneous Wapi lava field and the older Inferno Chasm vent and outflow channel, fall compositionally within the framework of eastern Snake River Plain olivine tholeiites. Total volume of lava in the Kings Bowl field is estimated to be 0.0125 km3, compared to a previous estimate of 0.005 km3. The main (central) lava lake lost a total of 0.0018 km3 of magma by either drain-back into the fissure system or breakout flows from breached levees. Phreatic explosions along the Kings Bowl fissure system occurred after magma supply was cut off, leading to fissure evacuation, and were triggered by magma withdrawal. The fissure system produced multiple phreatic explosions and the main pit is accompanied by others that occur as subordinate pits and linear blast corridors along the fissure. The drop in magma supply and the concomitant influx of groundwater were necessary processes that led to the formation of Kings Bowl and other pits along the fissure. A conceptual model is presented that has relevance to the broader range of low-volume, monogenetic

  17. The Effect of CO2 on Partial Reactive Crystallization of MORB-Eclogite-derived Basaltic Andesite in Peridotite and Generation of Silica-Undersaturated Basalts

    NASA Astrophysics Data System (ADS)

    Mallik, A.; Dasgupta, R.

    2012-12-01

    Recycled oceanic crust (MORB-eclogite) is considered to be the dominant heterogeneity in Earth's mantle. Because MORB-eclogite is more fusible than peridotite, siliceous partial melt derived from it must react with peridotite while the latter is still in the subsolidus state. Thus, studying such reactive process is important in understanding melting dynamics of the Earth's mantle. Reaction of MORB-eclogite-derived andesitic partial melt with peridotite can produce alkalic melts by partial reactive crystallization but these melts are not as silica-undersaturated as many natural basanites, nephelinites or melititites [1]. In this study, we constrain how dissolved CO2 in a siliceous MORB-eclogite-derived partial melt affects the reaction phase equilibria involving peridotite and can produce nephelinitic melts. Here we compare experiments on CO2-free [1] and 2.6 wt.% CO2 bearing andesitic melt+lherzolite mixtures conducted at 1375 °C and 3 GPa with added melt fraction of 8-50 wt.%. In both CO2-free and CO2-bearing experiments, melt and olivine are consumed and opx and garnet are produced, with the extent of modal change for a given melt-rock ratio being greater for the CO2-bearing experiments. While the residue evolves to a garnet websterite by adding 40% of CO2-bearing melt, the residue becomes olivine-free by adding 50% of the CO2-free melt. Opx mode increases from 12 to ~55 wt.% for 0 to 40% melt addition in CO2-bearing system and 12 to ~43 wt.% for 0 to 50% melt addition in CO2-free system. Garnet mode, for a similar range of melt-rock ratio, increases from ~10 to ~15 wt.% for CO2 bearing system and to ~11 wt.% for CO2-free system. Reacted melts from 25-33% of CO2-bearing melt-added runs contain ~39 wt.% SiO2 , ~11-13 wt.% TiO2, ~9 wt.% Al2O3, ~11 wt.% FeO*, 16 wt.% MgO, 10-11 wt.% CaO, and 3 wt.% Na2O whereas experiments with a similar melt-rock ratio in a CO2-free system yield melts with 44-45 wt.% SiO2, 6-7 wt.% TiO2, 13-14 wt.% Al2O3, 10-11 wt.% FeO*, 12-13 wt

  18. Reaction rim growth on olivine in silicic melts: Implications for magma mixing

    USGS Publications Warehouse

    Coombs, Michelle L.; Gardner, James E.

    2004-01-01

    Finely crystalline amphibole or pyroxene rims that form during reaction between silicic host melt and cognate olivine xenocrysts, newly introduced during magma mixing events, can provide information about the timing between mixing and volcanic eruptions. We investigated rim growth experimentally by placing forsteritic olivine in rhyolitic and rhyodacitic melts for times between 25 and 622 h at 50 and 150 MPa, H2O-saturated, at the Ni-NiO buffer. Rims of orthopyroxene microlites formed from high-silica rhyolite and rhyodacite melts at 885°C and 50 MPa, and in the rhyolite at 150 MPa and 885°C. Rims of amphibole with lesser orthopyroxene formed in the rhyolite at 150 MPa and 800°C and in the rhyodacite at 150 MPa and 885°C. Irregular, convolute olivine edges and mass balance between olivine, melt, and rim phases show that olivine partly dissolved at all conditions. Iron-rich zones at the exteriors of olivines, which increased in width parabolically with time, show that Fe-Mg interdiffusion occurring in olivines was not outpaced by olivine dissolution. Linear increases of the square of rim widths with time suggest that diffusion within the melt is the rate-controlling process for olivine dissolution and rim growth. Rims grew one-half to one order-of-magnitude faster when melt water contents were doubled, unless conditions were far above the liquidus. Rim growth rate in rhyolite increases from 0.055 ± 0.01 µm2/h at 885°C and 50 MPa to 0.64 ± 0.13 µm2/h at 800°C and 150 MPa. Melt composition has a lesser effect on rim growth rates, with growth rate increasing as melt SiO2 content decreases. Pyroxene rims on olivines in andesite erupted from Arenal volcano (Costa Rica) grew at a rate of 3.0 ± 0.2 µm2/h over an eleven-year period. This rate is faster than those of the experiments due to lower melt viscosity and higher temperatures, and suggests that a magma mixing event preceded the start of the eruption by days.

  19. 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.

  20. Short- and long-term olivine weathering in Svalbard: implications for Mars.

    PubMed

    Hausrath, E M; Treiman, A H; Vicenzi, E; Bish, D L; Blake, D; Sarrazin, P; Hoehler, T; Midtkandal, I; Steele, A; Brantley, S L

    2008-12-01

    Liquid water is essential to life as we know it on Earth; therefore, the search for water on Mars is a critical component of the search for life. Olivine, a mineral identified as present on Mars, has been proposed as an indicator of the duration and characteristics of water because it dissolves quickly, particularly under low-pH conditions. The duration of olivine persistence relative to glass under conditions of aqueous alteration reflects the pH and temperature of the reacting fluids. In this paper, we investigate the utility of 3 methodologies to detect silicate weathering in a Mars analog environment (Sverrefjell volcano, Svalbard). CheMin, a miniature X-ray diffraction instrument developed for flight on NASA's upcoming Mars Science Laboratory, was deployed on Svalbard and was successful in detecting olivine and weathering products. The persistence of olivine and glass in Svalbard rocks was also investigated via laboratory observations of weathered hand samples as well as an in situ burial experiment. Observations of hand samples are consistent with the inference that olivine persists longer than glass at near-zero temperatures in the presence of solutions at pH approximately 7-9 on Svalbard, whereas in hydrothermally altered zones, glass has persisted longer than olivine in the presence of fluids at similar pH at approximately 50 degrees C. Analysis of the surfaces of olivine and glass samples, which were buried on Sverrefjell for 1 year and then retrieved, documented only minor incipient weathering, though these results suggest the importance of biological impacts. The 3 types of observations (CheMin, laboratory observations of hand samples, burial experiments) of weathering of olivine and glass at Svalbard show promise for interpretation of weathering on Mars. Furthermore, the weathering relationships observed on Svalbard are consistent with laboratory-measured dissolution rates, which suggests that relative mineral dissolution rates in the laboratory, in

  1. V/Sc in olivine as a proxy for magma redox conditions

    NASA Astrophysics Data System (ADS)

    Locmelis, M.; Arevalo, R. D., Jr.; Puchtel, I. S.; Fiorentini, M. L.

    2017-12-01

    Although olivine is the most abundant mineral in the upper mantle and a major constituent of most mantle-derived rocks, studies on its trace element chemistry are underrepresented. This is especially the case for komatiites, an ultramafic, olivine-dominated rock type that formed via high degrees of partial melting (up to 50%) of the mantle. Komatiites were mostly emplaced in the Archean and therefore provide a unique perspective on the composition and evolution of the early Earth's mantle. Here, we present the V/Sc compositions of olivines from a global set of Paleo- (3.5-3.3 Ga) and Neo-Archean (2.7 Ga) komatiites analyzed via laser ablation ICP-MS. Vanadium and Sc behave similar during partial melting, but V is redox-sensitive (V2+-V5+) and most compatible in olivine as V2+. Scandium is monovalent (Sc3+) and its compatibility in olivine is not affected by the oxygen fugacity (fO2) of the komatiite lava. Therefore, V/Sc ratios in olivines are potentially indicative of the fO2 of the magma they crystallized from. Our data show that V/Sc ratios measured in Neo-Archean olivines (V/Scmean = 1.0 ± 0.1; 2σm) are significantly lower than in their Paleo-Archean counterparts (V/Scmean = 2.1 ± 0.1; 2σm). Geochemical models show that the elevated V/Sc ratios captured by the Paleo-Archean olivines reflect crystallization from magmas that were 1.6 log units (relative to QFM) more reduced than their Neo-Archean counterparts, and thus contained a higher proportion of V2+. Because assimilation of sedimentary bedrocks can alter the composition of komatiites upon emplacement, it may be argued that the redox states recorded by the olivines do not reflect mantle fO2, but the assimilation of crustal material. However, such an effect is not visible in our data as V/Sc ratios in olivines from localities that show evidence of crustal assimilation do not differ from komatiites that did not assimilate significant amounts of crustal rocks. Rather than a crustal signature, the V

  2. Hydrothermal alkali metal recovery process

    DOEpatents

    Wolfs, Denise Y.; Clavenna, Le Roy R.; Eakman, James M.; Kalina, Theodore

    1980-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by treating them with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of an added base to establish a pH during the treatment step that is higher than would otherwise be possible without the addition of the base. During the treating process the relatively high pH facilitates the conversion of water-insoluble alkali metal compounds in the alkali metal residues into water-soluble alkali metal constituents. The resultant aqueous solution containing water-soluble alkali metal constituents is then separated from the residue solids, which consist of the treated particles and any insoluble materials formed during the treatment step, and recycled to the gasification process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preferably, the base that is added during the treatment step is an alkali metal hydroxide obtained by water washing the residue solids produced during the treatment step.

  3. Time constraints on the origin of large volume basalts derived from O-isotope and trace element mineral zoning and U-series disequilibria in the Laki and Grímsvötn volcanic system

    NASA Astrophysics Data System (ADS)

    Bindeman, Ilya N.; Sigmarsson, Olgeir; Eiler, John

    2006-05-01

    The 1783-1784 AD fissure eruption of Laki (Iceland) produced 15 km 3 of homogeneous basaltic lavas and tephra that are characterized by extreme (3‰) 18O-depletion relative to normal mantle. Basaltic tephra erupted over the last 8 centuries and as late as in November 2004 from the Grímsvötn central volcano, which together with Laki are a part of a single volcanic system, is indistinguishable in δ18O from Laki glass. This suggests that all tap a homogeneous and long-lived low- δ18O magma reservoir. In contrast, we observe extreme oxygen isotope heterogeneity (2.2-5.2‰) in olivine and plagioclase contained within these lavas and tephra, and disequilibrium mineral-glass oxygen-isotope fractionations. Such low- δ18O glass values, and extreme 3‰ range in δ18O olivine have not been described in any other unaltered basalt. The energy constrained mass balance calculation involving oxygen isotopes and major element composition calls for an origin of the Laki-Grímsvötn quartz tholeiitic basaltic melts with δ18O = 3.1‰ by bulk digestion of low- δ18O hydrated basaltic crust with δ18O = - 4‰ to + 1‰, rather than magma mixing with ultra-low- δ18O silicic melt. The abundant Pleistocene hyaloclastites, which were altered by synglacial meltwaters, can serve as a likely assimilant material for the Grímsvötn magmas. The ( 226Ra / 230Th) activity ratio in Laki lavas and 20th century Grímsvötn tephras is 13% in-excess of secular equilibrium, but products of the 20th century Grímsvötn eruptions have equilibrium ( 210Pb / 226Ra). Modeling of oxygen isotope exchange between disequilibrium phenocrysts and magmas, and these short-lived U-series nuclides yields a coherent age for the Laki-Grímsvötn magma reservoir between 100 and 1000 yrs. We propose the existence of uniquely fingerprinted, low- δ18O, homogeneous, large volume, and long-lived basaltic reservoir beneath the Laki-Grímsvötn volcanic system that has been kept alive in its position above the

  4. Space Weathering in Olivine and the Mineralogy of (Some) M-Class Asteroids

    NASA Astrophysics Data System (ADS)

    Britt, Daniel; Kohout, Tomas; Schelling, Patrick; Consolmagno, Guy J.

    2014-11-01

    One aspect of space weathering of airless bodies is the production of nanophase iron (npFe0) from Fe bearing silicate minerals. The combined effects of low oxygen fugacity and solar-wind implanted H tend to result in strongly-reduced surfaces that can be chemically activated by heating due to micrometeorite impacts. The mineral kinetics of olivine makes it particularly vulnerable to reduction, decomposition, and npFe0 production. Kohout et al. has recently developed a new method of controlled npFe0 production on olivine powder grains that mimics the essential features of this weathering process and was developed to quantitatively evaluate spectral changes related to space weathering and presence of npFe0. Compared to fresh olivine the treated samples exhibit spectral characteristics of space weathering including spectral darkening, shallowing and attenuation of 1 µm olivine absorption band, and reddening. The attenuation of the 1 µm band significantly shrinks the band FWHM and shifts the much reduced band center to shorter wavelengths around 0.95 µm. These spectral changes are related to increasing amounts of npFe0 and the disruption of the crystal structure of the parent olivine. Significantly, the darkened, reddened, and band attenuated olivine spectra are a close match to a number of M-class asteroids. What is particularly interesting is the match with the weak absorption band near 0.95 µm seen in many M-class asteroids (i.e. 16 Psyche, 22 Kalliope, 55 Pandora to name a few). One of the major issues in asteroid science is the relative scarcity of olivine asteroids (the ”Great Dunite Shortage” coined by Bell et al in Asteroids II). One possibility worth further study is that asteroidal olivine may be hidden by the relative ease with which it weathers. The surface chemical and micrometeorite environment in the asteroid belt may produce over time a spectrum for an olivine-rich surface that is remarkably similar to that of an M-class asteroid.

  5. Shock-produced olivine glass: First observation

    USGS Publications Warehouse

    Jeanloz, R.; Ahrens, T.J.; Lally, J.S.; Nord, G.L.; Christie, J.M.; Heuer, A.H.

    1977-01-01

    Transmission electron microscope (TEM) observations of an experimentally shock-deformed single crystal of natural peridot, (Mg0.88Fe 0.12SiO4 recovered from peak pressures of about 56 ?? 109 pascals revealed the presence of amorphous zones located within crystalline regions with a high density of tangled dislocations. This is the first reported observation ofolivine glass. The shocked sample exhibits a wide variation in the degree of shock deformation on a small scale, and the glass appears to be intimately associated with the highest density of dislocations. This study suggests that olivine glass may be formed as a result of shock at pressures above about 50 to 55 ?? 109 pascals and that further TEM observations of naturally shocked olivines may demonstrate the presence of glass.

  6. EXTINGUISHMENT OF ALKALI METAL FIRES

    DTIC Science & Technology

    low O2 partial pressures on alkali metal fires Extinguishment of alkali metal fires using in organic salt mixtures Extinguishment of alkali metal ... fires using inorganic salt foams Alkali metal jet stream ignition at various pressure conditions Bibliography

  7. Sea water - basalt interactions and genesis of the coastal thermal waters of Maharashtra, India

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

    Muthuraman, K.

    1986-01-01

    The thermal waters close to the western coastal belt of India (in Maharashtra State) generally discharge Na-Ca-Cl and Ca-Na-Cl types of waters through the basic lava flows of late Cretaceous-early Tertiary age. Experimental work to study the reactions between the dilute sea water and basalt conducted in static autoclaves at selected elevated temperatures, indicates the possibility of producing chloride waters with relatively high calcium, similar to these thermal waters. In view of the increase in Ca in the resultant solutions during sea water-basalt reactions at elevated temperatures, the base temperatures computed by Na-K-Ca geothermometry would be far lower than themore » actual temperatures of the system. At lower temperatures (around 100/sup 0/C) absorption by K by basalt is possible and, hence, alkali geothermometry also may not be reliable for such systems. Anhydrite saturation temperature seems to be a reliable geothermometer for such coastal thermal water systems involving a sea water component. The results of the computer processing of the chemistry of some of these thermal waters using ''WATEQ'' are discussed. Two of these waters are oversaturated with diopside, tremolite, calcite and aragonite, indicating a rather low temperature of origin. In two other cases, interaction with ultramafic rocks is indicated, as these waters are oversaturated with diopside, tremolite, talc, chrysotile, sepiolite and its precipitate. There is no clear evidence to show that the thermal waters of the west coast of India emerge directly from either marine evaporites or oil field waters. It is proposed that the majority of these thermal waters should have originated through interaction of an admixture of sea water and meteoric water with the local basalt flows at some elevated temperatures.« less

  8. The alkaline volcanic rocks of Craters of the Moon National Monument, Idaho and the Columbia Hills of Gusev Crater, Mars

    NASA Astrophysics Data System (ADS)

    Neakrase, L. D.; Lim, D. S. S.; Haberle, C. W.; Hughes, S. S.; Kobs-Nawotniak, S. E.; Christensen, P. R.

    2016-12-01

    Idaho's Eastern Snake River Plain (ESRP) is host to extensive expressions of basaltic volcanism dominated by non evolved olivine tholeiites (NEOT) with localized occurrences of evolved lavas. Craters of the Moon National Monument (COTM) is a polygenetic lava field comprised of more than 60 lava flows emplaced during 8 eruptive periods spanning the last 15 kyrs. The most recent eruptive period (period A; 2500-2000 yr B.P.) produced flows with total alkali vs. silica classifications spanning basalt to trachyte. Coeval with the emplacement of the COTM period A volcanic pile was the emplacement of the Wapi and King's Bowl NEOT 70 km SSE of COTM along the Great Rift. Previous investigations have determined a genetic link between these two compositionally distinct volcanic centers where COTM compositions can be generated from NEOT melts through complex ascent paths and variable degrees of fractionation and assimilation of lower-middle crustal materials. The Mars Exploration Rover, Spirit, conducted a robotic investigation of Gusev crater from 2004-2010. Spirit was equipped with the Athena science payload enabling the determination of mineralogy (mini-Thermal Emission Spectrometer, Pancam multispectral camera, and Mössbauer spectrometer), bulk chemistry (Alpha Particle X-ray Spectrometer) and context (Pancam and Microscopic Imager). During sol 32 Spirit investigated an olivine basalt named Adirondack, the type specimen for a class of rock that composes much of the plains material within Gusev Crater and embays the Columbia Hills. Following the characterization of the plains material, Spirit departed the plains targeting the Columbia Hills and ascending at Husband Hill. During Spirit's ascent of Husband Hill three additional classes of volcanic rock were identified as distinct by their mini-TES spectra; Wishstone, Backstay and Irvine. These rocks are classified as tephrite, trachy-basalt and basalt, respectively, and are the first alkaline rocks observed on Mars. These

  9. Refractories for high alkali environments

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

    Rau, A.W.; Cloer, F.

    1996-12-31

    Information on refractories for high alkali environments is outlined. Information is presented on: product gallery; alkali attack; chemical reactions; basic layout of alkali cup test; criteria for rating alkali cup test samples; and basic layout of physical properties test.

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

    NASA Astrophysics Data System (ADS)

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

    2002-09-01

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

  11. Evidence for stable grain boundary melt films in experimentally deformed olivine-orthopyroxene rocks

    NASA Astrophysics Data System (ADS)

    de Kloe, R.; Drury, M. R.; van Roermund, H. L. M.

    The microstructure of olivine-olivine grain boundaries has been studied in experimentally deformed (1200-1227°C, 300MPa) partially molten olivine and olivine-orthopyroxene rocks. In-situ melting produced 1vol% melt in all samples studied. Grain boundary analyses were carried out using a number of transmission electron microscopy techniques. The grain boundary chemistry in undeformed olivine-orthopyroxene starting material showed evidence for the presence of an intergranular phase along some, but not all, of the olivine-olivine boundaries. In the deformed samples, ultrathin Si-rich, Al- and Ca-bearing amorphous films have been observed along all investigated olivine-olivine grain boundaries. The chemistry of the grain boundaries, which is considered to be indicative for the presence of a thin film, was measured with energy-dispersive X-ray spectroscopy (EDX) and energy-filtering imaging. The amorphous nature of the films was confirmed with diffuse dark field imaging, Fresnel fringe imaging, and high-resolution electron microscopy. The films range in thickness from 0.6 to 3.0nm, and EDX analyses show that the presence of Al and Ca is restricted to this ultrathin film along the grain boundaries. Because thin melt films have been observed in all the samples, they are thought to be stable features of the melt microstructure in deformed partially molten rocks. The transition from the occasional presence of films in the undeformed starting material to the general occurrence of the films in deformed materials suggests that deformation promotes the formation and distribution of the films. Alternatively, hot-pressing may be too short for films to develop along all grain boundaries. A difference in creep strength between the studied samples could not be attributed to grain boundary melt films, as these have been found in all deformed samples. However, a weakening effect of grain boundary melt films on olivine rheology could not be ruled out due to the lack of confirmed melt

  12. Determination of crystal residence timescales in magma reservoirs by diffusion modeling of dendritic phosphorus zoning patterns in olivine

    NASA Astrophysics Data System (ADS)

    Chakraborty, S.; Potrafke, A.

    2016-12-01

    ] indicate that dendritic crystal growth in such rapidly evolving dynamic environments should be considered as a widespread feature of olivine growth and evolution of many basaltic volcanic systems. [1] Watson et al., 2015, Am Min, 100, pp. 2053-2065 [2] Dohmen et al., 2007, Phys Chem Miner, 34(6), pp. 389-407 [3] Welsch et al., 2014, Geology, 42, pp. 867-870

  13. Fe/Mn in olivine of carbonaceous meteorites

    NASA Technical Reports Server (NTRS)

    Steele, Ian M.

    1993-01-01

    Olivines in primitive meteorites show a range of Fe/Mn both within one grain and among grains suggesting that they have recorded changing conditions during or after growth. Because olivine should be an early forming phase, Fe/Mn is used here to infer these earliest conditions. Initial Fe/Mn in cores of isolated, euhedral forsterite in both C2 and C3 meteorites ranges from 25 to 35 but differs at grain edge. Murchison (C2) forsterites show Fe/Mn approaching 1.0 at the grain edge while Ornans Fe/Mn is near 60 at grain edge. These values are lower than the matrix Fe/Mn for both meteorites and the distinct difference in zoning profile indicates different processes operating during and after grain growth. The Fe/Mn of bulk samples from a particular source such as the Moon is nearly constant. Individual samples show variation suggesting that there is some fractionation of Mn from Fe. Minerals have their individual ranges of Fe/Mn which has been used to recognize different types of olivine within one meteorite. Extreme values of Fe/Mn below 1.0 occur in forsterite from some IDP's, UOC matrix, and C1 meteorites. There are apparently no detailed studies of Fe/Mn variation within single olivine grains. Forsterite grains in C2 and C3 carbonaceous chondrites show complex zoning, and the nearly pure forsterites (Fo greater than approximately 99.5) have high levels of some minor elements including Ti, Al, V, and Sc. There is disagreement on the original source of these grains and both chondrule and vapor growth have been proposed. In addition, there is clear evidence that diffusion has affected the outer margins but in some cases the whole grain. Within the cores, the FeO range is limited, and if growing under constant conditions, the Fe/Mn should be near constant as there is little fractionation of Mn from Fe by forsterite. Additionally, there are apparently no co-crystallizing phases as evidenced by a lack of common inclusions in the forsterites. These observations are now

  14. Magma feeding system of Kutcharo and Mashu calderas, Hokkaido, Japan: Evidence of a common basaltic magma evolving into two distinct rock series

    NASA Astrophysics Data System (ADS)

    Miyagi, I.; Itoh, J.; Nguyen, H.

    2009-12-01

    Kutcharo and its adjacent Mashu volcanoes are located in NE Hokkaido, about 150 km west of the Kurile trench. The latest major activity of Kutcharo was 35 thousand years ago (termed KP I) produced about 50 km3 D.R.E, Mashu meanwhile became active after KP I. To understand the magma feeding system of adjoining but distinct Kutcharo (medium-K) and Mashu (low-K) volcanoes, we examined major and trace element, and Sr, Nd, and Pb isotopic compositions of whole rocks. We also studied phenocryst chemical zoning and chemical compositions of melt inclusions in phenocryst. The chemical results of melt inclusions show no distinction between medium- and low-K as being recognized in bulk rock chemistry of the volcanoes. Instead, the results form a smooth trend between low-K rock series and high-K rhyolitic melt end-member (as high as 5 wt. % K2O). There is no significant difference Sr, Nd and Pb isotopes between basalt and rhyolite suggesting genetic relationship. Moreover, the trace element distribution patterns show enrichment increasing gradually from the basalt to rhyolite via andesite indicating fractional crystallization evolution. Chemical zoning in plagioclase phenocryst in KP I (An 80-40) suggest that basaltic magma injected repeatedly into a voluminous felsic magma chamber of Kutcharo volcano. Chemical compositions of olivine phenocryst show that Kutcharo (Fo 86) was hotter as compared to Mashu (Fo 75). Application of MELTS program (Ghiorso and Sack, 1995) on composition of the basaltic melt end-member suggests that crystallization or subsequent re-melting of the basalt may produce medium- to high-K rhyolite melt, and mixing of the rhyolite with basalt may form the observed medium-K Kutcharo and low-K Mashu rock series. It is estimated that total volume of the basaltic magma supplied intermittently beneath the volcanoes was several folds to 10 times larger than the erupted rhyolite magma. And that the basalt injection may be more intensive beneath Kutcharo, leading to

  15. Optical absorption and radiative heat transport in olivine at high temperature

    NASA Technical Reports Server (NTRS)

    Shankland, T. J.; Nitsan, U.; Duba, A. G.

    1979-01-01

    Results are presented of measurements of the optical absorption spectra (300-8000 nm) of olivine as a function of temperature (300-1700 K) under conditions of controlled and known oxygen fugacity within the stability field of the samples. The absorption spectra are used to calculate the temperature-dependent radiative transfer coefficient of olivine and to numerically study the accuracy of the method. The present absorption measurements in olivine under oxidizing conditions known to be within the olivine stability field indicate that the effective radiative conductivity K(R) is lower than that obtained in previous studies under different experimental conditions. The lower value of K(R) makes it more likely that some of the earth's internal heat is removed by convection and less likely that thermal models involving conduction and radiation alone will satisfactorily explain thermal conditions in the earth's mantle.

  16. Hydrothermal alkali metal catalyst recovery process

    DOEpatents

    Eakman, James M.; Clavenna, LeRoy R.

    1979-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles primarily in the form of water soluble alkali metal formates by treating the particles with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of added carbon monoxide. During the treating process the water insoluble alkali metal compounds comprising the insoluble alkali metal residues are converted into water soluble alkali metal formates. The resultant aqueous solution containing water soluble alkali metal formates is then separated from the treated particles and any insoluble materials formed during the treatment process, and recycled to the gasification process where the alkali metal formates serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. This process permits increased recovery of alkali metal constituents, thereby decreasing the overall cost of the gasification process by reducing the amount of makeup alkali metal compounds necessary.

  17. 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.

  18. Dynamic crystallization study of barred olivine chondrules

    NASA Technical Reports Server (NTRS)

    Lofgren, Gary; Lanier, A. B.

    1990-01-01

    The 'classic' barred olivine (BO) texture was defined by Donaldson (1976) as a single-plate dendrite which shares the entire chondrule with the remaining glass or subsequent crystallization products. This paper describes experiments in which BO textures were produced experimentally from two starting compositions: one modeled after the average BO chondrule composition in L-chondrites determined by Weisberg (1987), and the other after an olivine-rich composition (CH-1) studied by Lofgren (1989). It is shown that most of the textural features observed in natural BO chondrules are replicated in the experimentally produced chondrules. Several new constraints on models for the chondrule-forming process are proposed.

  19. Relationships among basaltic lunar meteorites

    NASA Technical Reports Server (NTRS)

    Lindstrom, Marilyn M.

    1991-01-01

    During the past two years four meteorites of dominantly mare basalt composition were identified in the Japanese and US Antarctic collections. Basalts represent a much higher proportion of the lunar meteorites than is expected from photogeologic mapping of mare and highland regions. Also, the basaltic lunar meteorites are all described as VLT mare basalt, which is a relatively uncommon type among returned lunar samples. The significance of the basaltic meteorites to the understanding of the lunar crust depends on the evaluation of possible relationships among the individual meteorites. None of the specimens are paired meteorites. They differ from each other in petrography and composition. It is important to determine whether they might be paired ejecta which were ejected from the same mare region by the same impact. The question of paired ejecta must be addressed using a combination of exposure histories and petrographic/compositional characteristics. It is possible that the basaltic lunar meteorites are paired ejecta from the same region of the Moon. However, the relationships among them are more complicated than the basaltic breccias being simply brecciated mare gabbros.

  20. Origin of Permian OIB-like basalts in NW Thailand and implication on the Paleotethyan Ocean

    NASA Astrophysics Data System (ADS)

    Wang, Yuejun; He, Huiying; Zhang, Yuzhi; Srithai, Boontarika; Feng, Qinglai; Cawood, Peter A.; Fan, Weiming

    2017-03-01

    The basaltic rocks in NW Thailand belong to part of giant Southeast Asian igneous zone that delineates the extension of the Paleotethyan Ocean from SW China into NW Thailand. The Chiang Mai basaltic samples from the Chiang Dao, Fang, Lamphun and Ban Sahakorn sections are divisible into two groups of high-iron basalt. Group 1 has SiO2 of 38.30-49.18 wt.%, FeOt of 13.09-25.37 wt.%, MgO of 8.38-1.60 wt.%, TiO2 of 3.92-6.30 wt.%, which is rarely observed in nature. Group 2 shows SiO2 = 44.71-49.21 wt.%, FeOt = 10.88-14.34 wt.%, MgO = 5.24-16.11 wt.%, TiO2 = 2.22-3.07 wt.% and mg# = 44-70. Olivine and pyroxene are responsible for the fractionation of the Group 2 magma whereas low oxygen fugacity during the late-stage differentiation of the Group 1 magma prolonged fractionation of ilmenite and magnetite. The onset of ilmenite and magnetite fractionations controls the distinct differentiation commencing at MgO = 7 wt.%. Both groups show similar REE and primitive mantle-normalized patterns with insignificant Eu, Nb-Ta and Zr-Hf anomalies. They have similar Nd isotopic compositions with εNd (t) values ranging from + 2.8 to + 3.7 and similar Nb/La, Nb/U, Th/La, Zr/Nb, Th/Ta, La/Yb, Nb/Th, Nb/Y and Zr/Y, resembling those of OIB-like rocks. The representative basaltic sample yields the argon plateau age of 282.3 ± 1.4 Ma, suggestive of Early Permian origin. Our data argue for Group 1 and Group 2 are coeval in the intra-oceanic seamount setting within the Paleotethyan Ocean, which at least continued till 283 Ma. These data, along with other observations, suggest that the Inthanon zone defines the main Paleotethyan suture zone, which northerly links with the Changning-Menglian suture zone in SW China.

  1. Adirondack's Inner Self

    NASA Technical Reports Server (NTRS)

    2004-01-01

    This spectrum - the first taken of a rock on another planet - reveals the different iron-containing minerals that makeup the martian rock dubbed Adirondack. It shows that Adirondack is a type of volcanic rock known as basalt. Specifically, the rock is what is called olivine basalt because in addition to magnetite and pyroxene, two key ingredients of basalt, it contains a mineral called olivine. This data was acquired by Spirit's Moessbauer spectrometer before the rover developed communication problems with Earth on the 18th martian day, or sol, of its mission.

  2. Carbonate Mineralization of Volcanic Province Basalts

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

    Schaef, Herbert T.; McGrail, B. Peter; Owen, Antionette T.

    2010-03-31

    Flood basalts are receiving increasing attention as possible host formations for geologic sequestration of anthropogenic CO2, with studies underway in the United States, India, Iceland, and Canada. As an extension of our previous experiments with Columbia River basalt, basalts from the eastern United States, India, and South Africa were reacted with aqueous dissolved CO2 and aqueous dissolved CO2-H2S mixtures under supercritical CO2 (scCO2) conditions to study the geochemical reactions resulting from injection of CO2 in such formations. The results of these studies are consistent with cation release behavior measured in our previous experiments (in press) for basalt samples tested inmore » single pass flow through dissolution experiments under dilute solution and mildly acidic conditions. Despite the basalt samples having similar bulk chemistry, mineralogy and apparent dissolution kinetics, long-term static experiments show significant differences in rates of mineralization as well as compositions and morphologies of precipitates that form when the basalts are reacted with CO2-saturated water. For example, basalt from the Newark Basin in the United States was by far the most reactive of any basalt tested to date. Carbonate reaction products for the Newark Basin basalt were globular in form and contained significantly more Fe than the secondary carbonates that precipitated on the other basalt samples. In comparison, the post-reacted samples associated with the Columbia River basalts from the United States contained calcite grains with classic dogtooth spar morphology and trace cation substitution (Mg and Mn). Carbonation of the other basalts produced precipitates with compositions that varied chemically throughout the entire testing period. Examination of polished cross sections of the reacted grains by scanning electron microscopy and energy dispersive x-ray spectroscopy show precipitate overgrowths with varying chemical compositions. Compositional differences in

  3. Assessing Magmatic Processes and Hazards at two Basaltic Monogenetic Centers: Volcan Jorullo, Mexico, and Blue Lake Maar, Oregon

    NASA Astrophysics Data System (ADS)

    Johnson, E. R.; Cashman, K.; Wallace, P.; Delgado Granados, H.

    2007-05-01

    Although monogenetic basaltic volcanoes exhibit a wide variety of eruption styles, the origin of this diversity is poorly understood and often ignored when assessing volcanic hazards. To better understand magmatic processes and hazards associated with these eruptions, we have studied two monogenetic centers with differing behavior: Volcan Jorullo, a cinder cone in Mexico, and Blue Lake, a maar in the Oregon High Cascades. Although compositionally similar (medium-K basalt to basaltic andesite), their eruptive styles and products are quite different. Jorullo had violent strombolian eruptions that deposited alternating beds of ash and tephra, as well as lava flows. In contrast, Blue Lake exhibited initial phreatomagmatism that formed a 100m deep crater and produced surge deposits. This activity was followed by magmatic eruptions that produced deposits of tephra and bombs, but no lava flows. The diversity in eruptive style at these two centers reflects different magma ascent and crystallization processes, deduced using olivine-hosted melt inclusions. Jorullo melt inclusions trap variably degassed melts (0.5-5 wt% H2O; 0-1000 ppm CO2), with associated crystallization pressures that decrease from early (<4 kbars) to late (<100 bars) in the eruption. These data support the formation of a shallow storage region beneath the volcano that facilitated both crystallization and magma degassing, which is consistent with effusion of degassed lavas from the base of the cone throughout the eruption. In contrast, Blue Lake inclusions trap melts with a restricted range of volatiles (2.6-4 wt% H2O; 677-870 ppm CO2) corresponding to crystallization pressures of 2.2-3.2 kbars. This suggests that the magma feeding Blue Lake stalled in the upper crust and crystallized before ascending rapidly to the surface, without further crystallization of olivine or shallow storage. This is consistent with both the observed unstratified tephra deposits (indicating single rather than pulsatory eruptions

  4. Solar Radiation Management and Olivine Dissolution Methods in Climate Engineering

    NASA Astrophysics Data System (ADS)

    Kone, S.

    2014-12-01

    An overview of solar radiation management and olivine dissolution methods allows to discuss, comparatively, the benefits and consequences of these two geoengineering techniques. The combination of those two techniques allows to concomitantly act on the two main agents intervening in global warming: solar radiation and carbon dioxide. The earth surface temperature increases due mainly to carbon dioxide (a greenhouse gas) that keeps the solar radiation and causes the global warming. Two complementary methods to mitigate climate change are overviewed: SRM method, which uses injected aerosols, aims to reduce the amount of the inbound solar radiation in atmosphere; and olivine dissolution in water, a key chemical reaction envisaged in climate engineering , aiming to reduce the amount of the carbon dioxide in extracting it from atmosphere. The SRM method works on scenarios of solar radiation decrease and the olivine dissolution method works as a carbon dioxide sequestration method. Olivine dissolution in water impacts negatively on the pH of rivers but positively in counteracting ocean acidification and in transporting the silica in ocean, which has benefits for diatom shell formation.

  5. Deformation of a crystalline olivine aggregate containing two immiscible liquids: Implications for early core-mantle differentiation

    NASA Astrophysics Data System (ADS)

    Cerantola, V.; Walte, N. P.; Rubie, D. C.

    2015-05-01

    Deformation-assisted segregation of metallic and sulphidic liquid from a solid peridotitic matrix is a process that may contribute to the early differentiation of small planetesimals into a metallic core and a silicate mantle. Here we present results of an experimental study using a simplified system consisting of a polycrystalline Fo90-olivine matrix containing a small percentage of iron sulphide and a synthetic primitive MORB melt, in order to investigate whether the silicate melt enhances the interconnection and segregation of FeS liquid under deformation conditions at varying strain rates. The experiments have been performed at 2 GPa, 1450 °C and strain rates between 1 ×10-3s-1 to 1 ×10-5s-1. Our results show that the presence of silicate melt actually hinders the migration and segregation of sulphide liquid by reducing its interconnectivity. At low to moderate strain rates the sulphide liquid pockets preserved a roundish shape, showing the liquid behavior is governed mainly by surface tension rather than by differential stress. Even at the highest strain rates, insignificant FeS segregation and interconnection were observed. On the other hand the basaltic melt was very mobile during deformation, accommodating part of the strain, which led to its segregation from the matrix at high bulk strains leaving the sulphide liquid stranded in the olivine matrix. Hence, we conclude that deformation-induced percolation of sulphide liquid does not contribute to the formation of planetary cores after the silicate solidus is overstepped. A possible early deformation enhanced core-mantle differentiation after overstepping the Fe-S solidus is not possible between the initial formation of silicate melt and the formation of a widespread magma ocean.

  6. Discovery Of Low Oxygen Fugacity (fo2) Mineral And Fluid Phases In Lower Mantle -Derived Early Pulse Of The Deccan Flood Basalts

    NASA Astrophysics Data System (ADS)

    Basu, A. R.; Das, S.

    2017-12-01

    Estimation of Earth's lower mantle mineralogy and oxygen fugacity are principally based on indirect geophysical and experimental studies. According to these studies, the mantle becomes increasingly reducing from upper to lower mantle due to the distribution of ferric (Fe3+) and ferrous (Fe2+) iron in perovskite, the dominant mineral phase in the lower mantle. However, the natural occurrence of low oxygen fugacity (fO2), lower mantle mineral and fluid phases are rare, except some for discrete inclusions in superdeep diamonds. In this study, we document that some rocks associated with plume volcanism, such as the Deccan flood basalt volcanic province, preserve the lower mantle mineral phases. We document here unusual primary texture - bearing minerals in olivine-clinopyroxene bearing picrite intrusives associated with the Deccan Traps. The olivine and clinopyroxene of these rocks have high 3He/4He ratio (R/RA 14) as well as Nd, Sr and Pb isotopes identical to those of the Réunion plume, clearly indicating their lower mantle - derivation. These rocks are the initial pulse at 68Ma of the Deccan Trap eruption [1]. Presence of unusual exsolved lamella and rectangular, vermicular intergrowths of diopside and magnetite in olivine indicate a precursory phase with higher Fe3+. The diopside part in rectangular intergrowth show presence of hydrocarbon. Trails of small graphitic carbon crystals are also present both in the cores of these olivine and diopside. We suggest that the hydrocarbons are derived from the lower mantle having much lesser fO2 than the upper mantle. This study unequivocally indicates that direct lower mantle mineralogical signature, including their fo2 can be obtained from early pulse of plume volcanism. References: [1] Basu A R, Renne P R, Dasgupta D K, Teichmann F, Poreda R J, Science 261, 902 - 906; 1993.

  7. Diffusion Modeling of Cooling Rates of Relict Olivine in Semarkona Chondrules

    NASA Astrophysics Data System (ADS)

    Hewins, R. H.; Ganguly, J.; Mariani, E.

    2009-03-01

    Diffusive exchange profiles between relict olivine and melt-grown olivine in Semarkona Type IIA chondrules were oriented by EBSD to correct D. Results for Fe-Mg (D from Dohmen) and Cr (Ito and Ganguly) are concordant at 300°-400°C/hr.

  8. Diffusion of Water through Olivine and Clinopyroxene: Implications for Melt Inclusion Fidelity

    NASA Astrophysics Data System (ADS)

    Plank, T. A.; Lloyd, A. S.; Ferriss, E.

    2016-12-01

    The maximum H2O concentrations measured in olivine-hosted melt inclusions (MIs) from arc tephra fall within a narrow range of 3-5 wt%. A major question is whether this reflects parental water concentrations or diffusive exchange through the host crystal during storage and ascent. Laboratory experiments have shown that water can diffuse through 500 micron olivine in minutes to days at 1100°C. We have tested these predictions with a natural experiment using volatile (H2O, CO2, S) diffusion along melt embayments to constrain ascent rates during the 1974 eruption of Volcan Fuego to 5-8 minutes from 7 km depth [1]. Thus, olivine-hosted MIs may move from their storage region to the surface during some eruptions rapidly enough to retain almost all of their original water. Only the smallest MIs (< 30 microns) will lose any water during such fast ascent, even for the fastest diffusion mechanism through olivine. We have also assessed the potential for clinopyroxene (cpx) to retain water (as H+) during magma ascent. In the same 1974 Fuego deposits, cpx crystals show H-loss on their rims and even from their interiors. Such diffusive loss in 5-8 minutes requires rapid diffusion of H in cpx, comparable to olivine and melt, and consistent with our recent laboratory experiments dehydrating Fe-bearing cpx [2]. Although H-diffusion is dependent on the site occupancy, all sites may lose H rapidly in cpx with Mg# < 92.5. While cpx and olivine may lose H during ascent and degassing, olivine-hosted MIs stand a better chance of retaining water due to the very low partitioning of water in olivine (D 0.001). The most favorable conditions for faithful retention of parental water concentrations involve a) rapid ascent (< hr.) from H2O-undersaturated reservoirs (prior to major water degassing), b) minerals with low partition coefficients for water, c) large crystals (>500 microns) and large melt inclusions (>50 microns), and 4) rapid post-eruptive cooling (< 1min, clast sizes < 1 cm). The

  9. Alkali metal and alkali earth metal gadolinium halide scintillators

    DOEpatents

    Bourret-Courchesne, Edith; Derenzo, Stephen E.; Parms, Shameka; Porter-Chapman, Yetta D.; Wiggins, Latoria K.

    2016-08-02

    The present invention provides for a composition comprising an inorganic scintillator comprising a gadolinium halide, optionally cerium-doped, having the formula A.sub.nGdX.sub.m:Ce; wherein A is nothing, an alkali metal, such as Li or Na, or an alkali earth metal, such as Ba; X is F, Br, Cl, or I; n is an integer from 1 to 2; m is an integer from 4 to 7; and the molar percent of cerium is 0% to 100%. The gadolinium halides or alkali earth metal gadolinium halides are scintillators and produce a bright luminescence upon irradiation by a suitable radiation.

  10. Thermal Emission Spectroscopy of 1 Ceres: Evidence for Olivine

    NASA Technical Reports Server (NTRS)

    Witteborn, Fred. C.; Roush, Ted L.; Cohen, Martin

    1999-01-01

    Thermal emission spectra of the largest asteroid, 1 Ceres, obtained from the Kuiper Airborne Observatory display features that may provide information about its surface mineralogy. The emissivity, obtained by dividing the spectra by a standard thermal model, is compared with emissivity spectra of olivines and phyllosilicates deduced via Kirchoff's law from reflectivity measurements. The spectra provide a fairly good match to fine grained olivines (0 to 5 micrometer size range). The smoothness of the spectrum beyond 18 micrometers is an indication of particles smaller than 50 micrometers. While the abrupt rise in emissivity near 8 micrometers matches many silicates, the distinct emissivity minimum centered near 12.8 micrometers is consistant with iron-poor olivines, but not with phyllosilicates. It suggests the presence of opaques and does not exclude a mixture with organics and fine-grained phyllosilicates.

  11. Apparatus enables accurate determination of alkali oxides in alkali metals

    NASA Technical Reports Server (NTRS)

    Dupraw, W. A.; Gahn, R. F.; Graab, J. W.; Maple, W. E.; Rosenblum, L.

    1966-01-01

    Evacuated apparatus determines the alkali oxide content of an alkali metal by separating the metal from the oxide by amalgamation with mercury. The apparatus prevents oxygen and moisture from inadvertently entering the system during the sampling and analytical procedure.

  12. Remote compositional analysis of lunar olivine-rich lithologies with Moon Mineralogy Mapper (M3) spectra

    USGS Publications Warehouse

    Isaacson, P.J.; Pieters, C.M.; Besse, S.; Clark, R.N.; Head, J.W.; Klima, R.L.; Mustard, J.F.; Petro, N.E.; Staid, M.I.; Sunshine, J.M.; Taylor, L.A.; Thaisen, K.G.; Tompkins, S.

    2011-01-01

    A systematic approach for deconvolving remotely sensed lunar olivine-rich visible to near-infrared (VNIR) reflectance spectra with the Modified Gaussian Model (MGM) is evaluated with Chandrayaan-1 Moon Mineralogy Mapper (M 3) spectra. Whereas earlier studies of laboratory reflectance spectra focused only on complications due to chromite inclusions in lunar olivines, we develop a systematic approach for addressing (through continuum removal) the prominent continuum slopes common to remotely sensed reflectance spectra of planetary surfaces. We have validated our continuum removal on a suite of laboratory reflectance spectra. Suites of olivine-dominated reflectance spectra from a small crater near Mare Moscoviense, the Copernicus central peak, Aristarchus, and the crater Marius in the Marius Hills were analyzed. Spectral diversity was detected in visual evaluation of the spectra and was quantified using the MGM. The MGM-derived band positions are used to estimate the olivine's composition in a relative sense. Spectra of olivines from Moscoviense exhibit diversity in their absorption features, and this diversity suggests some variation in olivine Fe/Mg content. Olivines from Copernicus are observed to be spectrally homogeneous and thus are predicted to be more compositionally homogeneous than those at Moscoviense but are of broadly similar composition to the Moscoviense olivines. Olivines from Aristarchus and Marius exhibit clear spectral differences from those at Moscoviense and Copernicus but also exhibit features that suggest contributions from other phases. If the various precautions discussed here are weighed carefully, the methods presented here can be used to make general predictions of absolute olivine composition (Fe/Mg content). Copyright ?? 2011 by the American Geophysical Union.

  13. Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano, Hawaii

    NASA Astrophysics Data System (ADS)

    Bohrson, Wendy A.; Clague, David A.

    1988-10-01

    Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225° to 1350° C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045° and 1090° C. Comparisons of the abundance of K2O in plagioclase and the abundances of TiO2 and Fe2O3in spinel of xenoliths and mid-ocean ridge basalt, and a single 87Sr/ 86Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155° 230° C of cooling which took place over about 120 ka — the age of the youngest Hualalai tholeiitic basalt — yield maximum cooling rates of 1.3×10-3 1.91×10-3 °C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel.

  14. Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano, Hawaii

    USGS Publications Warehouse

    Bohrson, W.A.; Clague, D.A.

    1988-01-01

    Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225?? to 1350?? C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045?? and 1090?? C. Comparisons of the abundance of K2O in plagioclase and the abundances of TiO2 and Fe2O3in spinel of xenoliths and mid-ocean ridge basalt, and a single 87Sr/ 86Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155??-230?? C of cooling which took place over about 120 ka - the age of the youngest Hualalai tholeiitic basalt - yield maximum cooling rates of 1.3??10-3-1.91??10-3 ??C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel

  15. Constraints on Mantle Plume Melting Conditions in the Martian Mantle Based on Improved Melting Phase Relationships of Olivine-Phyric Shergottite Yamato 980459

    NASA Technical Reports Server (NTRS)

    Kiefer, Walter S.; Rapp, Jennifer F.; Usui, Tomohiro; Draper, David S.; Filiberto, Justin

    2016-01-01

    Martian meteorite Yamato 980459 (hereafter Y98) is an olivine-phyric shergottite that has been interpreted as closely approximating a martian mantle melt [1-4], making it an important constraint on adiabatic decompression melting models. It has long been recognized that low pressure melting of the Y98 composition occurs at extremely high temperatures relative to martian basalts (1430 degC at 1 bar), which caused great difficulties in a previous attempt to explain Y98 magma generation via a mantle plume model [2]. However, previous studies of the phase diagram were limited to pressures of 2 GPa and less [2, 5], whereas decompression melting in the present-day martian mantle occurs at pressures of 3-7 GPa, with the shallow boundary of the melt production zone occurring just below the base of the thermal lithosphere [6]. Recent experimental work has now extended our knowledge of the Y98 melting phase relationships to 8 GPa. In light of this improved petrological knowledge, we are therefore reassessing the constraints that Y98 imposes on melting conditions in martian mantle plumes. Two recently discovered olivine- phyric shergottites, Northwest Africa (NWA) 5789 and NWA 6234, may also be primary melts from the martian mantle [7, 8]. However, these latter meteorites have not been the subject of detailed experimental petrology studies, so we focus here on Y98.

  16. Pre-eruptive processes and timescales recorded in olivine crystals and melt inclusions from the 2007 caldera-forming eruption of Piton de la Fournaise (La Réunion Island)

    NASA Astrophysics Data System (ADS)

    Albert, H.; Costa Rodriguez, F.; Herrin, J. S.; Di Muro, A.; Metrich, N.

    2017-12-01

    Summit caldera collapse is a rare event at Piton de la Fournaise. One such event occurred in 2007 during one of the largest historic eruptions of more than 200 Mm3 of magma. Effusion of aphyric basalts initiated at the summit area in mid-February, followed by the migration of active vents in March and early April to progressively lower elevations. Collapse of a 1 km diameter summit caldera occurred on April 5th while effusion of crystal rich lava continued until May 1st. Here we investigate these events through timescales recorded in olivine crystals and their melt inclusions (MIs) using a diffusion modelling approach. Olivine crystals from the early tephra emitted just before caldera collapse and from the post caldera collapse lava display similar compositions and zoning patterns. Fo [%Fo=100*Mg/(Mg+Fe)] values range from ≈82 to ≈86 and the phenocrysts are complexly zoned including a reverse followed by normal zoning. Fo≈84 cores are surrounded by a Fo≈86 plateau. In contact with the surrounding matrix or MIs, crystals exhibit normal zoning toward values of Fo≈82-83. Phosphorus distribution revealed in 2D X-Ray maps shows complex patterns that can be interpreted as early skeletal growth likely responsible for entrapment of MIs. Diffusion modeling of Fo, Ca, and Ni reveals two distinct magma residence timescales recorded in olivine. The inner reversed-zoned profiles yield timescales of 1-2 years, while normally-zoned profiles at crystal rims and also adjacent to MIs yield timescales of only a few days. Modelling of the P zoning patterns is consistent with the 1-2 year timescales obtained from reversely-zoned profiles. H2O contents of olivine-hosted MIs range from 0.35-1.16 wt%. Selective loss of water in some MIs suggests diffusive re-equilibration between the MIs and host magma during ascent. We have applied H2O diffusion modeling to estimate timescales of water loss of a few days, consistent with the results of Fo/Ca/Ni modeling of olivine profiles. We

  17. High δ56Fe values in Samoan basalts

    NASA Astrophysics Data System (ADS)

    Konter, J. G.; Pietruszka, A. J.; Hanan, B. B.; Finlayson, V.

    2014-12-01

    Fe isotope fractionation spans ~0-0.4 permil in igneous systems, which cannot all be attributed to variable source compositions since peridotites barely overlap these compositions. Other processes may fractionate Fe isotopes such as variations in the degree of partial melting, magmatic differentiation, fluid addition related to the final stages of melt evolution, and kinetic fractionation related to diffusion. An important observation in igneous systems is the trend of increasing Fe isotope values against an index of magmatic fractionation (e.g. SiO2; [1]). The data strongly curve from δ56Fe >0.3 permil for SiO2 >70 wt% down to values around 0.09 permil from ~65 wt% down to 40 wt% SiO2 of basalts. However, ocean island basalts (OIBs) have a slightly larger δ56Fe variability than mid ocean ridge basalts (MORBs; [e.g. 2]). We present Fe isotope data on samples from the Samoan Islands (OIB) that have unusually high δ56Fe values for their SiO2 content. We rule out alteration by using fresh samples, and further test for the effects of magmatic processes on the δ56Fe values. In order to model the largest possible fractionation, unusually small degrees of melting with extreme fractionation factors are modeled with fractional crystallization of olivine alone, but such processing fails to fractionate the Fe isotopes to the observed values. Moreover, Samoan lavas likely also fractionated clinopyroxene, and its lower fractionation factor would limit the final δ56Fe value of the melt. We therefore suggest the mantle source of Samoan lavas must have had unusually high δ56Fe. However, there is no clear correlation with the highly radiogenic isotope signatures that reflect the unique source compositions of Samoa. Instead, increasing melt extraction correlates with lower δ56Fe values in peridotites assumed to be driven by the preference for the melt phase by heavy Fe3+, while high values may be related to metasomatism [3]. The latter would be in line with metasomatized

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

    NASA Astrophysics Data System (ADS)

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

    2001-12-01

    been analysed on the proton microprobe at CSIRO in Sydney. The main trace elements in the sulfide inclusions are Zn, Pb, Ag, and Se. Other trace elements are below detection limits, which are normally at a level of several ppm. Zn concentrations (120 +/- 40 ppm) in sulphides are similar to those in silicate melts. This indicates that separation of the sulfide melt does not affect Zn contents of silicate melts. On the contrary, Ag (30 +/- 10 ppm) and Pb (40 +/- 10 ppm) contents in sulphides are at least in order of magnitude higher than in the silicate melt, and thus separation of the immiscible sulfide melt can significantly decrease Pb and Ag contents of the silicate magma. The widespread occurrence of sulfide inclusions, which were also described in olivine phenocrysts from ocean island basalts, indicates common saturation at low pressure of mantle-derived magmas with reduced sulfur.

  19. Load relaxation of olivine single crystals

    NASA Astrophysics Data System (ADS)

    Cooper, Reid F.; Stone, Donald S.; Plookphol, Thawatchai

    2016-10-01

    Single crystals of ferromagnesian olivine (San Carlos, AZ, peridot; Fo88-90) have been deformed in both uniaxial creep and load relaxation under conditions of ambient pressure, T = 1500°C and pO2 = 10-10 atm; creep stresses were in the range 40 ≤ σ1 (MPa) ≤ 220. The crystals were oriented such that the applied stress was parallel to [011]c, which promotes single slip on the slowest slip system in olivine, (010)[001]. The creep rates at steady state match well the results of earlier investigators, as does the stress sensitivity (a power law exponent of n = 3.6). Dislocation microstructures, including spatial distribution of low-angle (subgrain) boundaries, additionally confirm previous investigations. Inverted primary creep (an accelerating strain rate with an increase in stress) was observed. Load relaxation, however, produced a singular response—a single hardness curve—regardless of the magnitude of creep stress or total accumulated strain preceding relaxation. The log stress versus log strain rate data from load-relaxation and creep experiments overlap to within experimental error. The load-relaxation behavior is distinctly different than that described for other crystalline solids, where the flow stress is affected strongly by work hardening such that a family of distinct hardness curves is generated, which are related by a scaling function. The response of olivine for the conditions studied, we argue, indicates flow that is rate limited by dislocation glide, reflecting specifically a high intrinsic lattice resistance (Peierls stress).

  20. Load Relaxation of Olivine Single Crystals

    NASA Astrophysics Data System (ADS)

    Cooper, R. F.; Stone, D. S.; Plookphol, T.

    2016-12-01

    Single crystals of ferromagnesian olivine (San Carlos, AZ, peridot; Fo90-92) have been deformed in both uniaxial creep and load relaxation under conditions of ambient pressure, T = 1500ºC and pO2 = 10-10 atm; creep stresses were in the range 40 ≤ σ1 (MPa) ≤ 220. The crystals were oriented such that the applied stress was parallel to [011]c, which promotes single slip on the slowest slip system in olivine, (010)[001]. The creep rates at steady state match well the results of earlier investigators, as does the stress sensitivity (a power-law exponent of n = 3.6). Dislocation microstructures, including spatial distribution of low-angle (subgrain) boundaries, additionally confirm previous investigations. Inverted primary creep (an accelerating strain rate with an increase in stress) was observed. Load-relaxation, however, produced a singular response—a single hardness curve—regardless of the magnitude of creep stress or total accumulated strain preceding relaxation. The log-stress v. log-strain rate data from load-relaxation and creep experiments overlap to within experimental error. The load-relaxation behavior is distinctly different that that described for other crystalline solids, where the flow stress is affected strongly by work hardening such that a family of distinct hardness curves is generated, which are related by a scaling function. The response of olivine for the conditions studied, thus, indicates flow that is rate-limited by dislocation glide, reflecting specifically a high intrinsic lattice resistance (Peierls stress).

  1. Electrical conductivity of partially-molten olivine aggregate and melt interconnectivity in the oceanic upper mantle

    NASA Astrophysics Data System (ADS)

    Laumonier, Mickael; Frost, Dan; Farla, Robert; Katsura, Tomoo; Marquardt, Katharina

    2016-04-01

    A consistent explanation for mantle geophysical anomalies such as the Lithosphere-Astenosphere Boundary (LAB) relies on the existence of little amount of melt trapped in the solid peridotite. Mathematical models have been used to assess the melt fraction possibly lying at mantle depths, but they have not been experimentally checked at low melt fraction (< 2 vol. %). To fill this gap, we performed in situ electrical conductivity (EC) measurement on a partially-molten olivine aggregate (Fo92-olivine from a natural peridotite of Lanzarote, Canary Islands, Spain) containing various amount of basaltic (MORB-like composition) melt (0 to 100%) at upper mantle conditions. We used the MAVO 6-ram press (BGI) combined with a Solartron gain phase analyser to acquire the electrical resistance of the sample at pressure of 1.5 GPa and temperature up to 1400°C. The results show the increase of the electrical conductivity with the temperature following an Arrhenius law, and with the melt fraction, but the effect of pressure between 1.5 and 3.0 GPa was found negligible at a melt fraction of 0.5 vol.%. The conductivity of a partially molten aggregate fits the modified Archie's law from 0.5 to 100 vol.%. At melt fractions of 0.25, 0.15 and 0.0 vol.%, the EC value deviates from the trend previously defined, suggesting that the melt is no longer fully interconnected through the sample, also supported by chemical mapping. Our results extend the previous results obtained on mixed system between 1 and 10% of melt. Since the melt appears fully interconnected down to very low melt fraction (0.5 vol.%), we conclude that (i) only 0.5 to 1 vol.% of melt is enough to explain the LAB EC anomaly, lower than previously determined; and (ii) deformation is not mandatory to enhance electrical conductivity of melt-bearing mantle rocks.

  2. Compositionally Controlled Volatile Content of Nominally Volatile-Free Minerals in the Continental Upper Mantle of Southern Gondwana (Patagonia & W. Antarctica)

    NASA Astrophysics Data System (ADS)

    Rooks, E. E.; Gibson, S. A.; Leat, P. T.; Petrone, C. M.

    2015-12-01

    H2O and F contents affect many physical and chemical properties of the upper mantle, including melting temperature and viscosity. These elements are hosted by hydrous and F-rich phases, and by modally abundant, nominally-anhydrous/halogen-free mantle minerals, which can potentially accommodate the entire volatile budget of the upper mantle. We present high-precision SIMS analyses of H2O, and F in mantle xenoliths hosted by recently-erupted (5-10 Ka) alkali basalts from south Patagonia (Pali Aike) and older (c. 25 Ma) alkali basalts from localities along the Antarctic Peninsula. Samples are well characterised peridotites and pyroxenites, from a range of depths in the off-craton lithospheric mantle. Minerals are relatively dry: H2O contents of olivine span 0-49 ppm, orthopyroxene 150-235 ppm and clinopyroxene 100-395 ppm, with highest concentrations found in spinel-garnet lherzolites from Pali Aike. These H2O concentrations fall within the global measured range for off-craton mantle minerals. H2O and F are correlated, and the relative compatibility of F in mantle phases is clinopyroxene>orthopyroxene>olivine. However, elevated F concentrations of 100-210 ppm are found in pyroxenites from two Antarctic localities. This elevated F content is not correlated with high H2O, suggesting that these rocks interacted with a F-rich melt. In clinopyroxenes, F concentration is correlated with Ti, and the ratio of M1Ti to M1Al + M1Cr, suggesting a charge balanced substitution. Consistency between samples (excepting high-F pyroxenites) suggests a constant F-budget, and that concentrations in clinopyroxenes are controlled by mineral chemistry. In orthopyroxene, F correlates with CaO, but no other major or minor elements. Large variability of H2O concentrations within samples is attributed to diffusive loss during ascent. Cl is negligible in all samples, indicating little or no influence of slab fluids from this long-lived subduction zone.

  3. Methods of recovering alkali metals

    DOEpatents

    Krumhansl, James L; Rigali, Mark J

    2014-03-04

    Approaches for alkali metal extraction, sequestration and recovery are described. For example, a method of recovering alkali metals includes providing a CST or CST-like (e.g., small pore zeolite) material. The alkali metal species is scavenged from the liquid mixture by the CST or CST-like material. The alkali metal species is extracted from the CST or CST-like material.

  4. Coatings on Atacama Desert Basalt: A Possible Analog for Coatings on Gusev Plains Basalt

    NASA Technical Reports Server (NTRS)

    Sutter, B.; Golden, D. C.; Amundson, R.; Chong-Diaz, G.; Ming, D. W.

    2007-01-01

    Surface coatings on Gusev Plains basalt have been observed and may contain hematite and nanophase Fe-oxides along with enrichments in P, S, Cl, and K relative to the underlying rock. The Gusev coatings may be derived from the dissolution of adhering soil and/or parent rock along with the addition of S and Cl from outside sources. Transient water for dissolution could be sourced from melting snow during periods of high obliquity, acid fog, and/or ground water (Haskin et al., 2005). Coatings on basalt in the hyper-arid (less than 2mm y(sup -1)) Atacama Desert may assist in understanding the chemistry, mineralogy and formation mechanisms of the Gusev basalt coatings. The Atacama Desert climate is proposed to be analogous to a paleo-Mars climate that was characterized by limited aqueous activity when the Gusev coatings could have formed. The objectives of this work are to (i) determine the chemical nature and extent of surface coatings on Atacama Desert basalt, and (ii) assess coating formation mechanisms in the Atacama Desert. Preliminary backscattered electron imaging of Atacama basalt thin-sections indicated that the coatings are as thick as 20 m. The boundary between the coating and the basalt labradorite, ilmenite, and augite grains was abrupt indicating that the basalt minerals underwent no chemical dissolution. The Atacama coatings have been added to the basalt instead of being derived from basalt chemical weathering. Semi-quantitative energy dispersive spectroscopy shows the coatings to be chemically homogeneous. The coating is depleted in Ca (0.9 wt% CaO) and enriched in K (1.3 wt.% K2O) and Si (69.1 wt.% SiO2) relative to the augite and labradorite grains. A dust source enriched in Si (e.g., poorly crystalline silica) and K and depleted in Ca appears to have been added to the basalt surface. Unlike the Gusev coatings, no P, S, and Cl enrichment was observed. However, Fe (3.2 wt.% FeO) was present in the Atacama coatings suggesting the present of Fe

  5. Cenozoic volcanic geology and probable age of inception of basin-range faulting in the southeasternmost Chocolate Mountains, California

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

    Crowe, B.M.

    1978-02-01

    A complex sequence of Oligocene-age volcanic and volcaniclastic rocks form a major volcanic center in the Picacho area of the southeasternmost Chocolate Mountains, Imperial County, California. Basal-volcanic rocks consist of lava flows and flow breccia of trachybasalt, pyroxene rhyodacite, and pyroxene dacite (32 My old). These volcanic rocks locally overlie fanglomerate and rest unconformably on pre-Cenozoic basement rocks. South and southeast of a prominent arcuate fault zone in the central part of the area, the rhyolite ignimbrite (26 My old) forms a major ash-flow sheet. In the southwestern part of the Picacho area the rhyolite ignimbrite interfingers with and ismore » overlain by dacite flows and laharic breccia. The rhyolite ignimbrite and the dacite of Picacho Peak are overlapped by lava flows and breccia of pyroxene andesite (25 My old) that locally rest on pre-Cenozoic basement rocks. The volcanic rocks of the Picacho area form a slightly bimodal volcanic suite consisting chiefly of silicic volcanic rocks with subordinate andesite. Late Miocene augite-olivine basalt is most similar in major-element abundances to transitional alkali-olivine basalt of the Basin and Range province. Normal separation faults in the Picacho area trend northwest and north parallel to major linear mountain ranges in the region. The areal distribution of the 26-My-old rhyolite ignimbrite and the local presence of megabreccia and fanglomerate flanking probable paleohighs suggest that the ignimbrite was erupted over irregular topography controlled by northwest- and north-trending probable basin-range faults. These relations date the inception of faulting in southeasternmost California at pre-26 and probably pre-32 My ago. A transition of basaltic volcanism in the area is dated at 13 My ago. 9 figures, 2 tables.« less

  6. Mineralogical study of brown olivine in Northwest Africa 1950 shergottite and implications for the formation mechanism of iron nanoparticles

    NASA Astrophysics Data System (ADS)

    Takenouchi, Atsushi; Mikouchi, Takashi; Kogure, Toshihiro

    2017-12-01

    Martian meteorites, in particular shergottites, contain darkened olivine (so-called "brown olivine") whose color is induced by iron nanoparticles formed in olivine during a shock event. The formation process and conditions of brown olivine have been discussed in the Northwest Africa 2737 (NWA 2737) chassignite. However, formation conditions of brown olivine in NWA 2737 cannot be applied to shergottites because NWA 2737 has a different shock history from that of shergottites. Therefore, this study observed brown olivine in the NWA 1950 shergottite and discusses the general formation process and conditions of brown olivine in shergottites. Our observation of NWA 1950 revealed that olivine is heterogeneously darkened between and within grains different from brown olivine in NWA 2737. XANES analysis showed that brown olivine contains small amounts of Fe3+ and TEM/STEM observation revealed that there is no SiO-rich phase around iron metal nanoparticles. These observations indicate that iron nanoparticles were formed by a disproportionation reaction of olivine (3Fe2+olivine → Fe0metal + 2Fe3+olivine + Volivine, where Volivine means a vacancy in olivine). Some parts of brown olivine show lamellar textures in SEM observation and Raman peaks in addition to those expected for olivine, implying that brown olivine experienced a phase transition (to e.g., ringwoodite). In order to induce heterogeneous darkening, heterogeneous high temperature of about 1500-1700 K and shock duration of at least 90 ms are required. This heterogeneous high temperature resulted in high postshock temperature (>900 K) inducing back-transformation of most high-pressure phases. Therefore, in spite of lack of high-pressure phases, NWA 1950 (= Martian meteorites with brown olivine) experienced higher pressure and temperature compared to other highly shocked meteorite groups.

  7. H Diffusion in Olivine and Pyroxene from Peridotite Xenoliths and a Hawaiian Magma Speedometer

    NASA Technical Reports Server (NTRS)

    Peslier, A. H.; Bizimis, M.

    2014-01-01

    Hydrogen is present as a trace element in olivine and pyroxene and its content distribution in the mantle results from melting and metasomatic processes. Here we examine how these H contents can be disturbed during decompression. Hydrogen was analyzed by FTIR in olivine and pyroxene of spinel peridotite xenoliths from Salt Lake Crater (SLC) nephelinites which are part of the rejuvenated volcanism at Oahu (Hawaii) [1,2]. H mobility in pyroxene resulting from spinel exsolution during mantle upwelling Most pyroxenes in SLC peridotites exhibit exsolutions, characterized by spinel inclusions. Pyroxene edges where no exsolution are present have less H then their core near the spinel. Given that H does not enter spinel [3], subsolidus requilibration may have concentrated H in the pyroxene adjacent to the spinel exsolution during mantle upwelling. H diffusion in olivine during xenolith transport by its host magma and host magma ascent rates Olivines have lower water contents at the edge and near fractures compared to at their core, while the concentrations of all other chemical elements appear homogeneous. This suggests that some of the initial water has diffused out of the olivine. Water loss from the olivine is thought to occur during host-magma ascent and xenolith transport to the surface [4-6]. Diffusion modeling matches best the data when the initial water content used is that measured at the core of the olivines, implying that mantle water contents are preserved at the core of the olivines. The 3225 cm(sup -1) OH band at times varies independantly of other OH bands, suggesting uneven H distribution in olivine defects likely acquired during mantle metasomatism just prior to eruption and unequilibrated. Diffusion times (1-48 hrs) combined with depths of peridotite equilibration or of magma start of degassing allow to calculate ascent rates for the host nephelinite of 0.1 to 27 m/s.

  8. Oceanization starts from below during continental rupturing in the northern Red Sea

    NASA Astrophysics Data System (ADS)

    Cai, Y.; Ligi, M.; Bonatti, E.; Bosworth, W.; Cipriani, A.; Palmiotto, C.; Rasul, N. M.; Ronca, S.; Sanfilippo, A.; Seyler, M.; Nomani, S.; AlQutub, A. S.

    2015-12-01

    The role of magmatism in continental rupturing and in the birth of a new ocean is not well understood. Continental rupture can take place with intense and voluminous volcanism, as in the Southern Red Sea or in a relatively amagmatic mode, as in the Northern Red Sea. Mantle upwelling and melting may be affected by the south to north decreasing opening rate of the Red Sea and by the influence of the Afar plume, also decreasing from south to north. The tholeiitic basalts of the Red Sea spreading system contrast with the extensive Cenozoic basaltic lava fields of the western part of the Arabian peninsula that form one of the largest alkali basalt provinces in the world. In order to establish possible relationship between the Red Sea rift evolution and the western Saudi Arabia intraplate alkali volcanism, field work was carried out on Lunayyir, Ishara, al Kura and Khaybar volcanic fields. Collected samples cover a wide range of chemical diversity (from olivine basalt to trachyte) and span over a 20 Ma interval. We attempt a comparison of the geochemistry of igneous rocks from western Arabia dykes and volcanic fields with those from the Red Sea axis and from the islands of Zabargad and Brothers in the northern Red Sea, that represent basaltic melts injected into the thinned continental crust before continental rupturing and initiation of seafloor spreading. Gabbros drilled in the western Red Sea and exposed on the Brothers islands suggest that continental break up in the northern Red Sea, a relatively non-volcanic rift, is preceded by intrusion of oceanic-type basaltic melts that crystallize at progressively shallower crustal depths as rifting progresses towards continental break-up. A seismic reflection profile running across the central part of the southern Thetis basin shows a ~5 km wide reflector that marks the roof of a magma chamber located ~3.5 km below seafloor. The presence of a few kilometers deep subrift magma chamber soon after the initiation of oceanic

  9. 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

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

    NASA Astrophysics Data System (ADS)

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

    2003-04-01

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

  11. Iron mineralogy and aqueous alteration from Husband Hill through Home Plate at Gusev Crater, Mars: Results from the Mössbauer instrument on the Spirit Mars Exploration Rover

    NASA Astrophysics Data System (ADS)

    Morris, R. V.; Klingelhöfer, G.; Schröder, C.; Fleischer, I.; Ming, D. W.; Yen, A. S.; Gellert, R.; Arvidson, R. E.; Rodionov, D. S.; Crumpler, L. S.; Clark, B. C.; Cohen, B. A.; McCoy, T. J.; Mittlefehldt, D. W.; Schmidt, M. E.; de Souza, P. A.; Squyres, S. W.

    2008-12-01

    Spirit's Mössbauer (MB) instrument determined the Fe mineralogy and oxidation state of 71 rocks and 43 soils during its exploration of the Gusev plains and the Columbia Hills (West Spur, Husband Hill, Haskin Ridge, northern Inner Basin, and Home Plate) on Mars. The plains are predominantly float rocks and soil derived from olivine basalts. Outcrops at West Spur and on Husband Hill have experienced pervasive aqueous alteration as indicated by the presence of goethite. Olivine-rich outcrops in a possible mafic/ultramafic horizon are present on Haskin Ridge. Relatively unaltered basalt and olivine basalt float rocks occur at isolated locations throughout the Columbia Hills. Basalt and olivine basalt outcrops are found at and near Home Plate, a putative hydrovolcanic structure. At least three pyroxene compositions are indicated by MB data. MB spectra of outcrops Barnhill and Torquas resemble palagonitic material and thus possible supergene aqueous alteration. Deposits of Fe3+-sulfate soil, located at Paso Robles, Arad, and Tyrone, are likely products of acid sulfate fumarolic and/or hydrothermal activity, possibly in connection with Home Plate volcanism. Hematite-rich outcrops between Home Plate and Tyrone (e.g., Montalva) may also be products of this aqueous activity. Low water-to-rock ratios (isochemical alteration) are implied during palagonite, goethite, and hematite formation because bulk chemical compositions are basaltic (SO3-free basis). High water-to-rock ratios (leaching) under acid sulfate conditions are implied for the high-SiO2 rock and soil in Eastern Valley and the float rock FuzzySmith, which has possible pyrite/marcasite as a hydrothermal alteration product.

  12. Compositional Zoning in Kilauea Olivine: A Geochemical Tool for Investigating Magmatic Processes at Hawaiian Volcanoes

    NASA Astrophysics Data System (ADS)

    Lynn, Kendra J.

    Olivine compositions and zoning patterns have been widely used to investigate the evolution of magmas from their source to the Earthfs surface. Modeling the formation of compositional zoning in olivine crystals has been used to retrieve timescales of magma residence, mixing, and transit. This dissertation is composed of three projects that apply diffusion chronometry principles to investigate how zoned olivine phenocrysts record magmatic processes at Hawaiian volcanoes. Olivine phenocrysts from K.lauea, the most active and thoroughly studied volcano in Hawaiei, are used to develop a better understanding of how Hawaiian olivine crystals record magmatic histories. This work begins by examining how crustal processes such as magma mixing and diffusive reequilibration can modify olivine compositions inherited from growth in parental magmas (Chapter 2). Diffusive re-equilibration of Fe-Mg, Mn, and Ni in olivine crystals overprints the chemical relationships inherited during growth, which strongly impacts interpretations about mantle processes and source components. These issues are further complicated by sectioning effects, where small (400 ƒEm along the c-axis) olivine crystals are more susceptible to overprinting compared to large (800 ƒEm) crystals. Olivine compositions and zoning patterns are then used to show that magmas during K.laueafs explosive Keanak.koei Tephra period (1500-1823 C.E.) were mixed and stored in crustal reservoirs for weeks to months prior to eruption (Chapter 3). Fe-Mg disequilibrium between olivine rims and their surrounding glasses show that a late-stage mixing event likely occurred hours to days prior to eruption, but the exact timescale is difficult to quantify using Fe-Mg and Ni diffusion. Lithium, a rapidly diffusing trace element in olivine, is modeled for the first time in a natural volcanic system to quantify this late-stage, short-duration mixing event (Chapter 4). Lithium zoning in olivine records both growth and diffusion processes

  13. Mars: Difference Between Lowland and Highland Basalts Confirms A Tendency Observed In Terrestrial and Lunar Basaltic Compositions

    NASA Astrophysics Data System (ADS)

    Kochemasov, G.

    Basalts are very widespread lithology on surfaces of terrestrial planets because their mantles, by general opinion, are predominantly basic in composition. Planetary sur- face unevennesses are often filled with this very fluid under high temperatures ma- terial. Basaltic compositions are however variable and this is helped by a wide iso- morphism of constituent minerals: Na-Ca feldspars and Fe-Mg dark minerals. Ratios between light and dark minerals as well as Fe/Mg ratios in dark minerals play an important role in regulation of basaltic densities. Rock density is a very important factor for constructing tectonic blocks in celestial bodies (Theorem 4, [1]). Angular momenta regulation of different level tectonic blocks in rotating bodies is more effec- tively fulfilled at the crustal level as this level has the longest radius. Thus, composition of crustal basalts is very sensitive to hypsometric (tectonic0 position of certain plan- etary blocks. At Earth oceanic hollows are filled with Fe-rich tholeiites (the deepest Pacific depression is filled with the richest in Fe tholeiites), on continents prevail com- paratively Mg-rich continental basalts. Mare basalts of the Moon are predominantly Fe,Ti-rich. At higher crustal levels appear less dense feldspar-rich, KREEP basalts. This tendency for martian basalts became clear after TES experiment on MGS [2]. The TES data on mineralogy of low-albedo regions show that type1 spectra belong to less dense basic rocks (feldspar 50%, pyroxene 25%) than type2 spectra (feldspar 35%, pyroxene + glass 35%). It means that the highland basaltoids are less dense than the lowland ones. It is interesting that the type1 spectral shape is similar to a spec- trum of the Deccan Traps flood basalts [2]. These continental basalts of the low-lying Indostan subcontinent are known to be relatively Fe-rich and approach the oceanic tholeiites. Global gravity, magnetic, basaltic composition data, available upto now for these bodies: Earth, Moon, Mars

  14. Alkali metal ion battery with bimetallic electrode

    DOEpatents

    Boysen, Dane A; Bradwell, David J; Jiang, Kai; Kim, Hojong; Ortiz, Luis A; Sadoway, Donald R; Tomaszowska, Alina A; Wei, Weifeng; Wang, Kangli

    2015-04-07

    Electrochemical cells having molten electrodes having an alkali metal provide receipt and delivery of power by transporting atoms of the alkali metal between electrode environments of disparate chemical potentials through an electrochemical pathway comprising a salt of the alkali metal. The chemical potential of the alkali metal is decreased when combined with one or more non-alkali metals, thus producing a voltage between an electrode comprising the molten the alkali metal and the electrode comprising the combined alkali/non-alkali metals.

  15. Computational studies of solid-state alkali conduction in rechargeable alkali-ion batteries

    DOE PAGES

    Deng, Zhi; Mo, Yifei; Ong, Shyue Ping

    2016-03-25

    The facile conduction of alkali ions in a crystal host is of crucial importance in rechargeable alkali-ion batteries, the dominant form of energy storage today. In this review, we provide a comprehensive survey of computational approaches to study solid-state alkali diffusion. We demonstrate how these methods have provided useful insights into the design of materials that form the main components of a rechargeable alkali-ion battery, namely the electrodes, superionic conductor solid electrolytes and interfaces. We will also provide a perspective on future challenges and directions. Here, the scope of this review includes the monovalent lithium- and sodium-ion chemistries that aremore » currently of the most commercial interest.« less

  16. Textural evidence bearing on the origin of isolated olivine crystals in C2 carbonaceous chondrites

    NASA Technical Reports Server (NTRS)

    Richardson, S. M.; Mcsween, H. Y., Jr.

    1978-01-01

    In some cases the mechanical competence of chondrules in carbonaceous chondrites has been reduced by alteration of their mesostasis glass to friable phyllosilicate, providing a mechanism by which euhedral olivines can be separated from chondrules. Morphological features of isolate olivine grains found in carbonaceous chondrites are similar to those of olivine phenocrysts in chondrules. These observations suggest that the isolated olivine grains formed in chondrules, by crystallization from a liquid, rather than by condensation from a vapor.

  17. Flood basalts and mass extinctions

    NASA Technical Reports Server (NTRS)

    Morgan, W. Jason

    1988-01-01

    There appears to be a correlation between the times of flood basalts and mass-extinction events. There is a correlation of flood basalts and hotspot tracks--flood basalts appear to mark the beginning of a new hotspot. Perhaps there is an initial instability in the mantle that bursts forth as a flood basalt but then becomes a steady trickle that persists for many tens of millions of years. Suppose that flood basalts and not impacts cause the environmental changes that lead to mass-extinctions. This is a very testable hypothesis: it predicts that the ages of the flows should agree exactly with the times of extinctions. The Deccan and K-T ages agree with this hypothesis; An iridium anomaly at extinction boundaries apparently can be explained by a scaled-up eruption of the Hawaiian type; the occurrence of shocked-quartz is more of a problem. However if the flood basalts are all well dated and their ages indeed agree with extinction times, then surely some mechanism to appropriately produce shocked-quartz will be found.

  18. Geochemical systematics of komatiite tholeiite and adakitic-arc basalt associations: The role of a mantle plume and convergent margin in formation of the Sandur Superterrane, Dharwar craton, India

    NASA Astrophysics Data System (ADS)

    Manikyamba, C.; Kerrich, R.; Khanna, T. C.; Keshav Krishna, A.; Satyanarayanan, M.

    2008-11-01

    The ˜ 2.7 Ga Sandur Superterrane is located within the central belt of the ˜ 2.6 Ga Closepet granite that divides the Dharwar craton into eastern and western sectors. The composite SST includes multiple terranes defined by distinct lithological associations, and metamorphic-deformational histories, demarked by accretionary structures. The Sultanpura volcanic terrane includes well preserved spinifex textured komatiites and komatiitic-basalts, with pillowed tholeiitic basalts. Komatiites and komatiitic-basalts have Mg# of 0.82-0.84 and 0.55-0.64 respectively, and plot near the olivine control line, whereas basalts have Mg# 0.53-0.69. All three volcanic types can be divided into two populations based on Nb/Th ratios: for rocks with Nb/Th < 8, there is covariation with Th, and (La/Sm) N interpreted to be the result of crustal assimilation fractional crystallization (AFC), whereas those rocks with Nb/Th > 8 plot along the Mid Oceanic Ridge Basalt-Oceanic Island Basalt array in Th/Yb vs. Nb/Yb coordinates. Collectively, the data are interpreted as signatures of a zoned mantle plume, having multiple sources that erupted through, or at the margin of, continental lithosphere. Felsic flows associated with arc basalts of the eastern felsic volcanic terrane, tectonically juxtaposed to the Sultanpura volcanic terrane, have adakitic compositional characteristics: elevated Al 2O 3 but low Yb (0.30-0.50 ppm) contents, coupled with high (La/Yb) N (43-71) and Zr/Sm (37-41) ratios, but low Nb/Ta (5-12). These features, in conjunction with mostly positive Eu anomalies, rule out detectable crustal contamination, such that adakitic flows and associated basalts and volcanogenic sedimentary rocks having normalized anomalies at Nb-Ta-P-Ti, represent an arc association. Consequently, the distinctive magmatic associations of the Sultanpura and eastern felsic volcanic terranes are consistent with the Sandur Superterrane being tectonic fragments of distinct continental and oceanic provenance

  19. Depleted and metasomatized oceanic lithosphere beneath La Palma, Canary Islands

    NASA Astrophysics Data System (ADS)

    Janisch, Astrid; Ntaflos, Theodoros

    2017-04-01

    Due to the inaccessibility of Earth's interior, xenoliths became the best possibility to study the chemical composition of the earth mantle as well as its various processes. Three samples out of the sample suite of mantle peridotites from San Antonio Volcano on La Palma, Canary Islands, have been chosen to illustrate three examples of diverse mantle metasomatic events. The first sample, a pyroxene-hornblende-peridotite, was influenced by an alkali-rich, silicic-hydrous undersaturated melt and/or fluid forming a conspicuous cross-cutting amphibole-apatite-dyke with several veins percolating through the rock. Forsterite content in olivine varies between 82.5 - 85.5 and 86.0 - 89.0, suggesting at least two different occurrences of metasomatic overprint. Clinopyroxenes are mostly found in association with amphibole and in textural equilibrium hinting that both minerals may have grown together, while orthopyroxene have only been found as remnant inclusions in olivine. These clinopyroxenes are Cr-Diopsides with En43.40-50.97-Wo43.99-48.64-Fs4.30-8.22 and Mg# between 85.54 and 92.36. Secondary clinopyroxenes are Ti-Augites with En39.86-46.81-Wo46.65-51.98-Fs5.86-8.72 and Mg# of 82.44 - 89.09. The second sample, a sp-dunite, is characterized by haüyne-bearing melt veins which clearly indicate host-basalt infiltration. The haüyne is always in contact with amphibole, spinel and clinopyroxene denoting that they have been formed at the same time because there is no evidence for reaction among these phases. The melt infiltration apparently took place prior to xenolith entrainment in the host basalt. Primary olivine has Fo content of 89.57 - 89.67 with NiO ranging from 0.32 - 0.334, in contrast Fo content in secondary olivine varies from 89.05 - 90.86 and NiO fluctuates between 0.24 - 0.31. Cr-Diopside compositions are in range of En41.63-47.05-Wo47.83-51-90-Fs4.93-6.64 and Mg# between 86.48 - 90.50. The third sample is also a sp-dunite and marked by a network of phlogopite

  20. A study on the dynamic interfacial tension of acidic crude oil/alkali (alkali-polymer) systems--

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

    Huang, Y.; Yang, P.; Qin, T.

    1989-01-01

    This paper describes the investigation of dynamic interfacial tension (DIFT) between the acidic Liao-He crude oil and two types of brine: a simple alkali system and a combined alkali-polymer system. It was found that interfacial tension (IFT) changed markedly with time and that the history of DIFT depended upon the concentration of alkali in the brine. The experimental results also showed that the IFT dropped dramatically as soon as the fresh oil contacted brine causing spontaneous emulsification to occur. The steady-state value of DIFT {gamma} st can be lower with the combined alkali-polymer system than with the simple alkali system.more » The results indicate that biopolymer is more effective than partially hydrolyzed polyacrylamide (PHPAM) for lowering {gamma} st and that Na{sub 2}Co{sub 1} causes a lower {gamma} st than NaOH in the combined alkali-polymer system. Optimized formulations containing Na{sub 2}CO{sub 3} added biopolymer can reduce {gamma} st by two orders of magnitude, and PHPAM can reduce {gamma} st by one order of magnitude. The interaction between alkali and polymer in the combined alkali-polymer system is discussed.« less

  1. Trace elements in ocean ridge basalts

    NASA Technical Reports Server (NTRS)

    Kay, R. W.; Hubbard, N. J.

    1978-01-01

    A study is made of the trace elements found in ocean ridge basalts. General assumptions regarding melting behavior, trace element fractionation, and alteration effects are presented. Data on the trace elements are grouped according to refractory lithophile elements, refractory siderophile elements, and volatile metals. Variations in ocean ridge basalt chemistry are noted both for regional and temporal characteristics. Ocean ridge basalts are compared to other terrestrial basalts, such as those having La/Yb ratios greater than those of chondrites, and those having La/Yb ratios less than those of chondrites. It is found that (1) as compared to solar or chondrite ratios, ocean ridge basalts have low ratios of large, highly-charged elements to smaller less highly-charged elements, (2) ocean ridge basalts exhibit low ratios of volatile to nonvolatile elements, and (3) the transition metals Cr through Zn in ocean ridge basalts are not fractionated more than a factor of 2 or 3 from the chondritic abundance ratios.

  2. Serpentinization and alteration in an olivine cumulate from the Stillwater Complex, Southwestern Montana

    USGS Publications Warehouse

    Page, N.J.

    1976-01-01

    Some of the olivine cumulates of the Ultramafic zone of the Stillwater Complex, Montana, are progressively altered to serpentine minerals and thompsonite. Lizardite and chrysotile developed in the cumulus olivine and postcumulus pyroxenes; thompsonite developed in postcumulus plagioclase. The detailed mineralogy, petrology, and chemistry indicate that olivine and plagioclase react to form the alteration products, except for H2O, without changes in the bulk composition of the rocks. ?? 1976 Springer-Verlag.

  3. Experimental testing of olivine-melt equilibrium models at high temperatures

    NASA Astrophysics Data System (ADS)

    Krasheninnikov, S. P.; Sobolev, A. V.; Batanova, V. G.; Kargaltsev, A. A.; Borisov, A. A.

    2017-08-01

    Data are presented on the equilibrium compositions of olivine and melts in the products of 101 experiments performed at 1300-1600°C, atmospheric pressure, and controlled oxygen fugacity by means of new equipment at the Vernadsky Institute. It was shown that the available models of the olivine-melt equilibrium describe with insufficient adequacy the natural systems at temperatures over 1400°C. The most adequate is the model by Ford et al. (1983). However, this model overestimates systematically the equilibrium temperature with underestimating by 20-40°C at 1450-1600°C. These data point to the need for developing a new, improved quantitative model of the olivine-melt equilibrium for high-temperature magnesian melts, as well as to the possibility of these studies on the basis of the equipment presented.

  4. Phase equilibrium constraints on the origin of basalts, picrites, and komatiites

    NASA Astrophysics Data System (ADS)

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

    1998-07-01

    Experimental phase equilibrium studies at pressures ranging from 1 atm to 10 GPa are sufficient to constrain the origin of igneous rocks formed along oceanic ridges and in hotspots. The major element geochemistry of MORB is dominated by partial crystallization at low pressures in the oceanic crust and uppermost mantle, forcing compliance with liquid compositions in low-pressure cotectic equilibrium with olivine, plagioclase and often augite too; parental magmas to MORB formed by partial melting, mixing, and pooling have not survived these effects. Similarly, picrites and komatiites can transform to basalts by partial crystallization in the crust and lithosphere. However, parental picrites and komatiites that were successful in erupting to the surface typically have compositions that can be matched to experimentally-observed anhydrous primary magmas in equilibrium with harzburgite [L+Ol+Opx] at 3.0 to 4.5 GPa. This pressure is likely to represent an average for pooled magmas that collected at the top of a plume head as it flattened below the lithosphere. There is substantial uniformity in the normative olivine content of primary magmas at all depths in a plume melt column, and this results in pooled komatiitic magmas that are equally uniform in normative olivine. However, the imposition of pressure above 3 GPa produces picrites and komatiites with variations in normative enstatite and Al 2O 3 that reveal plume potential temperature and depths of initial melting. Hotter plumes begin to melt deeper than cooler plumes, yielding picrites and komatiites that are enriched in normative enstatite and depleted in Al 2O 3 because of a deeper column within which orthopyroxene can dissolve during decompression. Pressures of initial melting span the 4 to 10 GPa range, increasing in the following order: Iceland, Hawaii, Gorgona, Belingwe, Barberton. Parental komatiites and picrites from a single plume also exhibit internal variability in normative enstatite and Al 2O 3

  5. A Glass Spherule of Questionable Impact Origin from the Apollo 15 Landing Site: Unique Target Mare Basalt

    NASA Technical Reports Server (NTRS)

    Ryder, Graham; Delano, John W.; Warren, Paul H.; Kallemeyn, Gregory W.; Dalrymple, G. Brent

    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 microns-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 basaits. 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 Ar-40/Ar-39 laser incremental heating technique, is 1647 +/- 11 Ma (2 sigma); it is expressed as an age spectrum of seventeen steps over 96% of the Ar-38 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; Ar-38 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 is required to avoid crystallization, and barely attainable in such a large spherule. The low volatile abundances, slightly high siderophile

  6. Uranium-lead systematics of low-Ti basaltic meteorite Dhofar 287A: Affinity to Apollo 15 green glasses

    NASA Astrophysics Data System (ADS)

    Terada, Kentaro; Sasaki, Yu; Anand, Mahesh; Sano, Yuji; Taylor, Lawrence A.; Horie, Kenji

    2008-06-01

    Dhofar 287 is a lunar meteorite found in Oman in 2001, which consists of a major portion (95%) of low-Ti mare basalt (Dho 287A) and a minor attached part (˜ 5%) of regolith breccia (Dho 287B). Here, we report the U-Pb systematics of Dho 287A using data collected with a Sensitive High Resolution Ion Microprobe (SHRIMP). In-situ analyses of five merrillite and three apatite grains, which are resistant to secondary petrologic events, resulted in a total Pb/U isochron age of 3.34 ± 0.20 Ga, in 238U/206Pb-207Pb/206Pb-204Pb/206Pb 3-D space (95% confidence level). The observed Pb-Pb isochron of these eight phosphates coupled with four plagioclase grains also yielded a 207Pb/206Pb age of 3.35 ± 0.13 Ga. This formation age, when considered as the crystallization age of Dho 287A, is similar to crystallization ages of Apollo 15 low-Ti olivine-normative basalts (ONB; 3.3 ± 0.1 Ga). However, the estimated μ-value (238U/204Pb ratio) of Dho 287A is ˜ 18, which is very different from the reported μ-values of ˜ 300 for mare basalts from the Apollo collections, including the Apollo 15 ONBs. These μ-values are still significantly lower than those of Apollo KREEP basalt (500 to 1000), although a possible assimilation with KREEP has been previously proposed for Dho 287A using geochemical criteria. Our U-Pb study of Dho 287A, instead, indicates a closer affinity to Apollo 15 green glasses (207Pb/206Pb age of 3.41 Ga with μ-value of 19 to 55), which are considered to be the most primitive products of lunar volcanism. Combining our U-Pb data with the previously reported Sm-Nd systematics (negative ɛNd) of Dho 287A clearly distinguishes this meteorite from those of the Yamato 793169 and Asuka 88175 group which have extremely low μ-value of 10-22, old crystallization ages of 3.9 Ga, and high positive ɛNd, suggesting that Dho 287A may be a representative of an entirely new group of mare basalt derived from previously unsampled source region on the Moon.

  7. Crystallization of primitive basaltic magmas at crustal pressures and genesis of the calc-alkaline igneous suite: experimental evidence from St Vincent, Lesser Antilles arc

    NASA Astrophysics Data System (ADS)

    Pichavant, M.; MacDonald, R.

    2007-11-01

    Near-liquidus crystallization experiments have been carried out on two basalts (12.5 and 7.8 wt% MgO) from Soufriere, St Vincent (Lesser Antilles arc) to document the early stages of differentiation in calc-alkaline magmas. The water-undersaturated experiments were performed mostly at 4 kbar, with 1.6 to 7.7 wt% H2O in the melt, and under oxidizing conditions (ΔNNO = -0.8 to +2.4). A few 10 kbar experiments were also performed. Early differentiation of primitive, hydrous, high-magnesia basalts (HMB) is controlled by ol + cpx + sp fractionation. Residual melts of typical high-alumina basalt (HAB) composition are obtained after 30-40% crystallization. The role of H2O in depressing plagioclase crystallization leads to a direct relation between the Al2O3 content of the residual melt and its H2O concentration, calibrated as a geohygrometer. The most primitive phenocryst assemblage in the Soufriere suite (Fo89.6 olivine, Mg-, Al- and Ti-rich clinopyroxene, Cr-Al spinel) crystallized from near-primary (Mg# = 73.5), hydrous (˜5 wt% H2O) and very oxidized (ΔNNO = +1.5-2.0) HMB liquids at middle crustal pressures and temperatures from ˜1,160 to ˜1,060°C. Hornblende played no role in the early petrogenetic evolution. Derivative HAB melts may contain up to 7-8 wt% dissolved H2O. Primitive basaltic liquids at Soufriere, St Vincent, have a wide range of H2O concentrations (2-5 wt%).

  8. New Insights From Whole Rock and Mineral Data on the Magmatic and Tectonic Evolution of the Columbia River Basalt Group (USA)

    NASA Astrophysics Data System (ADS)

    Caprarelli, G.; Reidel, S. P.

    2004-12-01

    The Miocene Columbia River Basalt Group (CRBG) of north-western USA was emplaced in a geologically dynamic setting characterized by a close association between magmatism and lithospheric thinning and rifting. We present and discuss electron probe microanalysis and XRFA data obtained from samples spanning the entire sequence of the CRBG. The examined basalts have near-aphyric textures. No glass is present, and plagioclase and augitic clinopyroxene are dominant matrix and groundmass phases. Plagioclase microcrysts are labradoritic to bytownitic. Whole rock compositions were taken as proxies of the liquid compositions. Application of plagioclase / melt and clinopyroxene / melt geothermobarometers indicated that during crustal ascent the magmas were dry, and that pre-eruptive pressures and temperatures ranged from 0 to 0.66 GPa and 1393 to 1495 K, respectively. In a P-T diagram most of the samples are distributed along a general CRBG trend, while some samples plot along a parallel higher temperature trend. The calculated P-T values, the positive correlation between calculated P and T, and no horizontal alignment of the data, exclude the presence of upper crustal solidification fronts, and indicate that magma aggregation zones were located deeper than 25 km, plausibly immediately below the Moho, that in this region is at a depth of approximately 35 km. Episodic stretching of the lithosphere best explains the observed parallel P-T trends. Whole rock major element abundances resulted from fractional crystallization of the magmas during ascent. To retrieve the compositions of the primitive melts we added to the bulk rock compositions variable amounts of magnesian olivine [Mg/(Mg+Fe) = 0.88], and derived the evolution of olivine fractionating magmas in equilibrium with mantle harzburgite. Two groups of samples were found, corresponding to the parallel P-T trends obtained from mineral / melt calculations. The highest temperature trend corresponds to samples whose calculated

  9. Temperature Dependence and Recoil-free Fraction Effects in Olivines Across the Mg-Fe Solid Solution

    NASA Technical Reports Server (NTRS)

    Sklute, E. C.; Rothstein, Y.; Dyar, M. D.; Schaefer, M. W.; Menzies, O. N.; Bland, P. A.; Berry, F. J.

    2005-01-01

    Olivine and pyroxene are the major ferromagnesian minerals in most meteorite types and in mafic igneous rocks that are dominant at the surface of the Earth. It is probable that they are the major mineralogical components at the surface of any planetary body that has undergone differentiation processes. In situ mineralogical studies of the rocks and soils on Mars suggest that olivine is a widespread mineral on that planet s surface (particularly at the Gusev site) and that it has been relatively unaffected by alteration. Thus an understanding of the characteristics of Mossbauer spectra of olivine is of great importance in interpreting MER results. However, variable temperature Mossbauer spectra of olivine, which are needed to quantify recoil-free fraction effects and to understand the temperature dependence of olivine spectra, are lacking in the literature. Thus, we present here a study of the temperature dependence and recoil-free fraction of a series of synthetic olivines.

  10. Effect of the Hydrothermal Fluid Composition on the Serpentinization of Olivine and Pyroxene

    NASA Astrophysics Data System (ADS)

    Daniel, I.; Andreani, M.

    2016-12-01

    The hydrothermal alteration of ultramafic rocks leads to the serpentinization reaction that mainly forms serpentine and variable amounts of talc, brucite and magnetite, as well as hydrogen and magnesite when carbonate is present in the fluid. The serpentinization kinetics of pyroxene under hydrothermal conditions has been very little studied in comparison with olivine, and both have been evaluated experimentally only in simple aqueous fluids. Here, we have evaluated the effect of the fluid chemistry - aluminum, carbonate and pH on the serpentinization rate of olivine and orthopyroxene at 200 °C, 340 °C and 200 MPa to simulate natural hydrothermal conditions. We used low-pressure diamond-anvil cells (lp-DAC) and time-resolved X-ray diffraction to monitor in situ the progress of serpentinization in twelve experiments. We also performed several complementary long-lasting experiments of several days in particular with orthopyroxene, for which in situ monitoring was not possible. At 340 °C in presence of Al and/or carbonate and at high pH, olivine conversion into lizardite is extremely fast with a half-time reaction t1/2 = 2 hrs only, while orthopyroxene did not react much even after 6 days (11%). In contrast to olivine, orthopyroxene conversion to serpentine was faster without Al (48 % in 6 days). Magnetite was also observed to form in the runs with olivine at 340 °C and moderate pH. In experiments run with orthopyroxene only, we observed the exclusive formation of proto-serpentine instead of lizardite. We propose that the contrasted effect of Al on the serpentinization rate of olivine and orthopyroxene results from the complexation of Al in the solution that reacts differently with the mineral surfaces during their dissolution. The positively charged olivine surface allows the adsorption of the dominant negatively charged Al(OH)4- complex, while the neutral surface of orthopyroxene does not. This adsorption process could facilitate both the dissolution of olivine

  11. EXTINGUISHMENT OF ALKALI METAL FIRES

    DTIC Science & Technology

    Contents: Effect of inert gas nket and ow O2 partial pressures on alkali metal fires Extinguishment of small scale fires Extinguishment of alkali... metal fires using inorganic salt foam Alkali metal jet stream ignition at various pressure conditions

  12. Alkali resistant optical coatings for alkali lasers and methods of production thereof

    DOEpatents

    Soules, Thomas F; Beach, Raymond J; Mitchell, Scott C

    2014-11-18

    In one embodiment, a multilayer dielectric coating for use in an alkali laser includes two or more alternating layers of high and low refractive index materials, wherein an innermost layer includes a thicker, >500 nm, and dense, >97% of theoretical, layer of at least one of: alumina, zirconia, and hafnia for protecting subsequent layers of the two or more alternating layers of high and low index dielectric materials from alkali attack. In another embodiment, a method for forming an alkali resistant coating includes forming a first oxide material above a substrate and forming a second oxide material above the first oxide material to form a multilayer dielectric coating, wherein the second oxide material is on a side of the multilayer dielectric coating for contacting an alkali.

  13. Moessbauer spectra of olivine-rich achondrites - Evidence for preterrestrial redox reactions

    NASA Technical Reports Server (NTRS)

    Burns, R. G.; Martinez, S. L.

    1991-01-01

    Moessbauer spectral measurements at 4.2 K were made on several ureilites and the two shergottites found in Antarctica, as well as two ureilite falls, three SNC meteorite falls, and two finds in order to distinguish products of preterrestrial redox reactions from phases formed during oxidative weathering on the earth. The spectra indicated that several ureilites contain major proportions of metallic iron, much of which resulted from preterrestrial carbon-induced reduction of ferrous iron in the outermost 10-100 microns of olivine grains in contact with carbonaceous material in the ureilites. The cryptocrystalline nature of these Fe inclusions in olivine renders the metal extremely vulnerable to aerial oxidation, even in ureilites collected as falls. It is inferred that the nanophase ferric oxides or oxyhydroxides identified in Brachina and Lafayette were produced by terrestrial weather of olivines before the meteorites were found. The absence of goethite in two olivine-bearing Antarctic shergottites suggests that the 2 percent ferric iron determined in their Moessbauer spectra also originated from oxidation on Mars.

  14. Optical spectroscopic characterizations of laser irradiated olivine grains

    NASA Astrophysics Data System (ADS)

    Yang, Yazhou; Zhang, Hao; Wang, Ziwei; Yuan, Ye; Li, Shaolin; Hsu, Weibiao; Liu, Chujian

    2017-01-01

    Context. Visible and near-infrared spectra of asteroids are known to be susceptible to nanophase irons produced by space weathering processes, thus making mineral identifications difficult. Mid-infrared spectroscopy may retain more mineral features owing to its lattice vibrational nature. Aims: We investigate the structure and reflectance spectral feature changes of olivine grains before and after simulated space weathering. Methods: We irradiate olivine grains by using pulsed laser to simulate varying degrees of micrometeorite bombardments. Reflectance measurements from 0.5 to 25 μm and radiative transfer calculations were carried out in order to compare them with each other. Results: Both the experimental simulations and modeling results indicate that the mid-infrared spectral features of olivine grains can survive the intense irradiations. Although the Christansen Feature is slightly shifted to longer wavelength, major vibrational bands remain essentially unchanged, because the lattice structure is quite immune to even the strongest irradiations, as revealed by both the X-ray diffraction and Raman scattering measurements. Conclusions: Mid-infrared spectroscopy is much more immune to productions of nanophase irons and amorphous materials and thus may be used more reliably in remote detections of minerals on asteroid surfaces.

  15. Space Weathering of Olivine in Lunar Soils: A Comparison to Itokawa Regolith Samples

    NASA Technical Reports Server (NTRS)

    Keller, L. P.; Berger, E. L.

    2014-01-01

    Regolith particles from airless bodies preserve a record of the space weathering processes that occurred during their surface exposure history. These processes have major implications for interpreting remote-sensing data from airless bodies. Solar wind irradiation effects occur in the rims of exposed grains, and impact processes result in the accumulation of vapordeposited elements and other surface-adhering materials. The grains returned from the surface of Itokawa by the Hayabusa mission allow the space weathering "style" of a chondritic, asteroidal "soil" to be compared to the lunar case. Here, we present new studies of space-weathered olivine grains from lunar soils, and compare these results to olivine grains from Itokawa. Samples and Methods: We analyzed microtome thin sections of olivine grains from the 20-45 micron fractions of three lunar soils: 71061, 71501 and 10084 (immature, submature and mature, respectively). Imaging and analytical data were obtained using a JEOL 2500SE 200kV field-emission scanning-transmission electron microscope equipped with a thin-window energy-dispersive x-ray spectrometer. Similar analyses were obtained from three Hayabusa olivine grains. Results and Discussion: We observed lunar grains showing a range of solar flare track densities (from <10(exp 9) to approx.10(exp 12)/sq cm). The lunar olivines all show disordered, highly strained, nanocrystalline rims up to 150-nm thick. The disordered rim thickness is positively correlated with solar flare track density. All of the disordered rims are overlain by a Si-rich amorphous layer, ranging up to 50-nm thick, enriched in elements that are not derived from the host olivine (e.g., Ca, Al, and Ti). The outmost layer represents impact-generated vapor deposits typically observed on other lunar soil grains. The Hayabusa olivine grains show track densities <10(exp 10)/sq cm and display disordered rims 50- to 100-nm thick. The track densities are intermediate to those observed in olivines

  16. RELICT OLIVINES IN MICROMETEORITES: PRECURSORS AND INTERACTIONS IN THE EARTH’S ATMOSPHERE

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

    Rudraswami, N. G.; Prasad, M. Shyam; Dey, S.

    2016-11-10

    Antarctica micrometeorites (∼1200) and cosmic spherules (∼5000) from deep sea sediments are studied using electron microscopy to identify Mg-rich olivine grains in order to determine the nature of the particle precursors. Mg-rich olivine (FeO < 5wt%) in micrometeorites suffers insignificant chemical modification during its history and is a well-preserved phase. We examine 420 forsterite grains enclosed in 162 micrometeorites of different types—unmelted, scoriaceous, and porphyritic—in this study. Forsterites in micrometeorites of different types are crystallized during their formation in solar nebula; their closest analogues are chondrule components of CV-type chondrites or volatile rich CM chondrites. The forsteritic olivines are suggestedmore » to have originated from a cluster of closely related carbonaceous asteroids that have Mg-rich olivines in the narrow range of CaO (0.1–0.3wt%), Al{sub 2}O{sub 3} (0.0–0.3wt%), MnO (0.0–0.3wt%), and Cr{sub 2}O{sub 3} (0.1–0.7wt%). Numerical simulations carried out with the Chemical Ablation Model (CABMOD) enable us to define the physical conditions of atmospheric entry that preserve the original compositions of the Mg-rich olivines in these particles. The chemical compositions of relict olivines affirm the role of heating at peak temperatures and the cooling rates of the micrometeorites. This modeling approach provides a foundation for understanding the ablation of the particles and the circumstances in which the relict grains tend to survive.« less

  17. New Insights on the Rheology of Olivine Deformed under Lithospheric Temperature Conditions

    NASA Astrophysics Data System (ADS)

    Cordier, P.; Demouchy, S. A.; Mussi, A.; Tommasi, A.

    2014-12-01

    Rheology of mantle rocks at lithospheric temperatures remains poorly constrained, since most experimental studies on creep mechanisms of olivine single crystals ((MgFe)2SiO4, Pbnm) and polycrystalline olivine aggregates were performed at high-temperatures (T >> 1200oC). In this study, we report results from deformation experiments on oriented single crystals of San Carlos olivine and polycrystalline olivine aggregate at temperatures relevant of the uppermost mantle (ranging from 800o to 1090oC) in tri-axial compression. The experiments were carried out at a confining pressure of 300 MPa in a high-resolution gas-medium mechanical testing apparatus at various constant strain rates (from 7 x 10-6 s-1 to 1 x 10-4 s-1). Mechanical tests show that mantle lithosphere is actually weaker than previously inferred from the extrapolation of high-temperature experiments. In this study, we present characterization of dislocation microstructures based on transmission electron microscopy and electron tomography. It is shown that below 1000°C, dislocation activity is restricted to [001] glide with a strong predominance of {110} as glide planes. We observe recovery mechanisms which suggest that the mechanical properties observed in laboratory experiments represent an upper bound for the actual behavior of olivine under lithospheric mantle conditions. Moreover, the drastic reduction in slip system activity observed questions the ability of deforming olivine aggregates in the ductile regime at such temperatures. We show that ductility is preserved thanks to the activation of alternative deformation mechanisms in grain boundaries involving disclinations.

  18. Meeting the Continental Crust: the Hidden Olivine Trauma in Subduction Settings

    NASA Astrophysics Data System (ADS)

    Salas Reyes, P.; Ruprecht, P.; Rabbia, O. M.; Hernandez, L.

    2017-12-01

    In a conventional framework, olivine zonation represents concentric growth from an evolving liquid. Alternatively, it has been suggested (e.g. Welsch et al. 2014) that olivine develop dendritic textures and compositional discontinuities due to rapid growth and boundary layer effects, respectively, where any complex zoning is quickly erased through diffusive re-equilibration in the high temperature magmatic environment. In particular, olivine crystals from large volcanic centers in convergent margins rarely preserve such dendritic textures and complex zoning due prolonged magma residence. Small volume, mafic monogenetic vents may bypass such crustal re-equilibration and potentially record the otherwise elusive early olivine growth history. We selected tephra deposits from Los Hornitos, in the Andean arc of Central Chile (35.5˚S), that represents primitive magmas ( 15 wt.% MgO) and contain magnesian olivines (Fo>88) hosting quenched melt inclusions. We obtained detailed quantitative EPMA zoning profiles and measured volatile contents (H, C, S, Cl) in the co-existing melt inclusions. Furthermore, we analyzed mineral morphologies connecting compositional zoning with growth textures. We find that 40% of the olivine crystals retain dendritic shapes while the others are polyhedral with trapped melt inclusions and cavities. The polyhedral crystals are normally zoned (Fo92 to Fo88; Ni 4000 ppm to 1000 ppm), however an oscillatory zonation depicted by concentric -coupled Fo and Ni- enriched layers exist and therefore even those crystals still preserve also a more complete growth history. The related melt inclusions yield values of up to 6000 ppm of S. Such zonation may imply sudden growth during elevated degrees of undercooling (-ΔT > 60°C) as the magmas transit from the hot mantle to the cooler conditions in the crust. Moreover, the preservation of such Fo and Ni zonation requires limited time between crystal growth and eruption. The elevated S content in melt inclusions

  19. Petrological constraints on the high-Mg basalts from Capo Marargiu (Sardinia, Italy): Evidence of cryptic amphibole fractionation in polybaric environments

    NASA Astrophysics Data System (ADS)

    Tecchiato, Vanni; Gaeta, Mario; Mollo, Silvio; Scarlato, Piergiorgio; Bachmann, Olivier; Perinelli, Cristina

    2018-01-01

    This study deals with the textural and compositional characteristics of the calc-alkaline stratigraphic sequence from Capo Marargiu Volcanic District (CMVD; Sardinia island, Italy). The area is dominated by basaltic to intermediate hypabyssal (dikes and sills) and volcanic rocks (lava flows and pyroclastic deposits) emplaced during the Oligo-Miocene orogenic magmatism of Sardinia. Interestingly, a basaltic andesitic dome hosts dark-grey, crystal-rich enclaves containing up 50% of millimetre- to centimetre-sized clinopyroxene and amphibole crystals. This mineral assemblage is in equilibrium with a high-Mg basalt recognised as the parental magma of the entire stratigraphic succession at CMVD. Analogously, centimetre-sized clots of medium- and coarse-grained amphibole + plagioclase crystals are entrapped in andesitic dikes that ultimately intrude the stratigraphic sequence. Amphibole-plagioclase cosaturation occurs at equilibrium with a differentiated basaltic andesite. Major and trace element modelling indicates that the evolutionary path of magma is controlled by a two-step process driven by early olivine + clinopyroxene and late amphibole + plagioclase fractionation. In this context, enclaves represent parts of a cumulate horizon segregated at the early stage of differentiation of the precursory high-Mg basalt. This is denoted by i) resorption effects and sharp transitions between Mg-rich and Mg-poor clinopyroxenes, indicative of pervasive dissolution phenomena followed by crystal re-equilibration and overgrowth, and ii) reaction minerals found in amphibole coronas formed at the interface with more differentiated melts infiltrating within the cumulate horizon, and carrying the crystal-rich material with them upon eruption. Coherently, the mineral chemistry and phase relations of enclaves indicate crystallisation in a high-temperature, high-pressure environment under water-rich conditions. On the other hand, the upward migration and subsequent fractionation of the

  20. Low temperature dissolution creep induced B-type olivine fabric during serpentinization and deformation in mantle wedge

    NASA Astrophysics Data System (ADS)

    Liu, W.; Zhang, J.

    2017-12-01

    The B-type olivine fabric (i.e., the [010]ol axes subnormal to foliation and the [001]ol axes subparallel to the lineation) has been regarded as an important olivine fabric for interpreting global trench-parallel S-wave polarization in fore-arc regions. However, strong serpentinization and cold temperature environment in the mantle wedge should inhibit development of the B-type olivine fabric that requires high temperature to activate solid-state plastic deformation. Here we report fabrics of olivine and antigorite generated at low temperatures (300-370 oC) during serpentinization in a fossil mantle wedge of the Val Malenco area, Central Alps. Olivine in the serpentine matrix develops a pronounced B-type fabric, while antigorite in the same matrix displays a strong crystallographic orientation (CPO) with the (001) and the [010] subparallel to foliation and lineation, respectively. The following evidence leads to the conclusion that the B-type olivine fabric is resulted from dissolution creep assisted by grain boundaries sliding (GBS) and grain rotation, rather than solid-state plastic deformation: (1) serpentinization took place at low temperatures and a fluid-enriched environment, ideal for dissolution-precipitation creep; (2) the voids and zigzag boundaries along the interface between antigorite and olivine suggest a fluid dissolution reaction; (3) the primary coarse olivine develops a nearly random fabric, indicating the B-type fabrics in the fine-grained olivine can't be inherited fabrics. These results document for the first time the B-type olivine CPO formed by dissolution creep at low temperatures during serpentinization and provide a mechanism to reconcile petrofabric observations with geophysical observations of trench parallel fast S-wave seismic anisotropy in fore-arc mantle wedge regions.

  1. New constraints on Xe incorporation mechanisms in olivine from first-principles calculations

    NASA Astrophysics Data System (ADS)

    Crépisson, Céline; Blanchard, Marc; Lazzeri, Michele; Balan, Etienne; Sanloup, Chrystèle

    2018-02-01

    Storage of Xe at depth in silicate minerals has recently been proposed to explain the low Xe abundance in the Earth's and Mars' atmospheres compared to other noble gases (the so-called 'Missing Xenon' issue). Evidences for incorporation, and thus reactivity of Xe in olivine at high pressure and high temperature are based on variations in cell parameters and the appearance of a new Raman band. To constrain the, so far only hypothetical, Xe incorporation mechanism in olivine, we theoretically investigated models of Xe-bearing olivine using density functional theory. Three types of incorporation mechanisms are tested: Xe for Si and Xe for Mg substitutions, and interstitial Xe. Xe for Si substitution, implying an oxidation of Xe, is found to be the only mechanism consistent with experimental observations, leading to an increase of cell parameter a and the appearance of a new Raman band around 720-750 cm-1 associated with Xesbnd O stretching vibrations. Raman spectroscopy makes it possible to identify Xe incorporation site, even at low Xe content, due to high Xe polarizability. An estimation of Xe content in olivine, based on present work and previous in situ experimental results, shows that up to 0.4 at.% Xe could be stored in olivine at depth.

  2. Olivine-Orthopyroxene Equilibrium in Metal-rich Systems: Applications to Achondrites and Equilibrated Chondrites

    NASA Technical Reports Server (NTRS)

    Lauretta, D. S.; Benedix, G. K.; McCoy, T. J.

    2003-01-01

    Olivine and orthopyroxene are major minerals in every type of stony meteorite. The majority of achondritic meteorites and silicate-bearing iron meteorites have experienced high temperatures. If these temperatures persisted for an extended period of time then the iron contents of olivine and orthopyroxene should be in equilibrium. In their study of ungrouped clasts and chondritic meteorites, suggested that the equilibrium compositions of olivine and orthopyroxene should fall on a mixing line between LL chondrites and aubrites. Here we show that this is not necessarily the case and that a range of FeO contents in olivine and orthopyroxene can be in equilibrium with each other. The key parameters that determine the equilibrium Fe content in these minerals are temperature, oxygen fugacity (fO2), and silica activity (aSiO2).

  3. Experimental Melting Study of Basalt-Peridotite Hybrid Source: Melting model of Hawaiian plume

    NASA Astrophysics Data System (ADS)

    Takahashi, E.; Gao, S.

    2015-12-01

    Eclogite component entrained in ascending plume is considered to be essentially important in producing flood basalts (e.g., Columbia River basalt, Takahashi et al., 1998 EPSL), alkalic OIBs (e.g., Kogiso et al.,2003), ferro-picrites (Tuff et al.,2005) and Hawaiian shield lavas (e.g., Hauri, 1996; Takahashi & Nakajima, 2002, Sobolev et al.,2005). Size of the entrained eclogite, which controls the reaction rates with ambient peridotite, however, is very difficult to constrain using geophysical observation. Among Hawaiian shield volcanoes, Koolau is the most enriched end-member in eclogite component (Frey et al, 1994). Reconstruction of Koolau volcano based on submarine study on Nuuanu landslide (AGU Monograph vol.128, 2002, Takahashi Garcia Lipman eds.) revealed that silica-rich tholeiite appeared only at the last stage (Makapuu stage) of Koolau volcano. Chemical compositions of lavas as well as isotopes change abruptly and coherently across a horizon (Shinozaki et al. and Tanaka et al. ibid.). Based on these observation, Takahashi & Nakajima (2002 ibid) proposed that the Makapuu stage lava in Koolau volcano was supplied from a single large eclogite block. In order to study melting process in Hawaiian plume, high-pressure melting experiments were carried out under dry and hydrous conditions with layered eclogite/peridotite starting materials. Detail of our experiments will be given by Gao et al (2015 AGU). Combined previous field observation with new set of experiments, we propose that variation in SiO2 among Hawaiian tholeiites represent varying degree of wall-rock interaction between eclogite and ambient peridotite. Makapuu stage lavas in Koolau volcano represents eclogite partial melts formed at ~3 GPa with various amount of xenocrystic olivines derived from Pacific plate. In other words, we propose that "primary magma" in the melting column of Hawaiian plume ranges from basaltic andesite to ferro-picrite depending on the lithology of the source. Solidus of

  4. Correlations Between Olivine Abundance and Thermal Inertia: Implications for Global Weathering and/or Alteration on Mars

    NASA Astrophysics Data System (ADS)

    Hamilton, V. E.; McDowell, M. L.; Koeppen, W. C.

    2010-03-01

    TES data show no global trend between thermal inertia and olivine abundance. But it is premature to conclude that all dark surfaces were once more mafic OR that olivine is not preferentially removed from olivine-enriched outcrops as they erode.

  5. Alkali metal for ultraviolet band-pass filter

    NASA Technical Reports Server (NTRS)

    Mardesich, Nick (Inventor); Fraschetti, George A. (Inventor); Mccann, Timothy A. (Inventor); Mayall, Sherwood D. (Inventor); Dunn, Donald E. (Inventor); Trauger, John T. (Inventor)

    1993-01-01

    An alkali metal filter having a layer of metallic bismuth deposited onto the alkali metal is provided. The metallic bismuth acts to stabilize the surface of the alkali metal to prevent substantial surface migration from occurring on the alkali metal, which may degrade optical characteristics of the filter. To this end, a layer of metallic bismuth is deposited by vapor deposition over the alkali metal to a depth of approximately 5 to 10 A. A complete alkali metal filter is described along with a method for fabricating the alkali metal filter.

  6. Basaltic cannibalism at Thrihnukagigur volcano, Iceland

    NASA Astrophysics Data System (ADS)

    Hudak, M. R.; Feineman, M. D.; La Femina, P. C.; Geirsson, H.

    2014-12-01

    Magmatic assimilation of felsic continental crust is a well-documented, relatively common phenomenon. The extent to which basaltic crust is assimilated by magmas, on the other hand, is not well known. Basaltic cannibalism, or the wholesale incorporation of basaltic crustal material into a basaltic magma, is thought to be uncommon because basalt requires more energy than higher silica rocks to melt. Basaltic materials that are unconsolidated, poorly crystalline, or palagonitized may be more easily ingested than fully crystallized massive basalt, thus allowing basaltic cannibalism to occur. Thrihnukagigur volcano, SW Iceland, offers a unique exposure of a buried cinder cone within its evacuated conduit, 100 m below the main vent. The unconsolidated tephra is cross-cut by a NNE-trending dike, which runs across the ceiling of this cave to a vent that produced lava and tephra during the ~4 Ka fissure eruption. Preliminary petrographic and laser ablation inductively coupled mass spectrometry (LA-ICP-MS) analyses indicate that there are two populations of plagioclase present in the system - Population One is stubby (aspect ratio < 1.7) with disequilibrium textures and low Ba/Sr ratios while Population Two is elongate (aspect ratio > 2.1), subhedral to euhedral, and has much higher Ba/Sr ratios. Population One crystals are observed in the cinder cone, dike, and surface lavas, whereas Population Two crystals are observed only in the dike and surface lavas. This suggests that a magma crystallizing a single elongate population of plagioclase intruded the cinder cone and rapidly assimilated the tephra, incorporating the stubbier population of phenocrysts. This conceptual model for basaltic cannibalism is supported by field observations of large-scale erosion upward into the tephra, which is coated by magma flow-back indicating that magma was involved in the thermal etching. While the unique exposure at Thrihnukagigur makes it an exceptional place to investigate basaltic

  7. Shock-induced fine-grained recrystallization of olivine - Evidence against subsolidus reduction of Fe/2+/

    NASA Technical Reports Server (NTRS)

    Ahrens, T. J.; Tsay, F.-D.; Live, D. H.

    1976-01-01

    Electron spin resonance (ESR) studies have been carried out on three single grains of terrestrial olivine (Fo90) shock loaded along the 010 line to peak pressures of 280, 330, and 440 kbar. The results indicate that neither metallic Fe similar to that observed in returned lunar soils nor paramagnetic Fe(3+) caused by oxidation of Fe(2+) has been produced in these shock experiments. Trace amounts of Mn (2+) have been detected in both shocked and unshocked olivine. The ESR signals of Mn(2+) show spectral features which are found to correlate with the degree of shock-induced recrystallization observed petrographically. The increasing mass fraction of recrystallized olivine correlates with increasing shock pressures. This phenomenon is modelled assuming it results from the progressive effect of the shock-induced transformation of the olivine to a yet unknown high-pressure phase and its subsequent reversion to the low-pressure olivine phase. The mass fraction of recrystallized material is predicted to be nearly linear with shock pressure.

  8. Lithium isotope fractionation by diffusion in minerals Part 2: Olivine

    NASA Astrophysics Data System (ADS)

    Richter, Frank; Chaussidon, Marc; Bruce Watson, E.; Mendybaev, Ruslan; Homolova, Veronika

    2017-12-01

    Recent experiments have shown that lithium isotopes can be significantly fractionated by diffusion in silicate liquids and in augite. Here we report new laboratory experiments that document similarly large lithium isotopic fractionation by diffusion in olivine. Two types of experiments were used. A powder-source method where lithium from finely ground spodumene (LiAlSi2O6) diffused into oriented San Carlos olivine, and piston cylinder annealing experiments where Kunlun clinopyroxene (∼30 ppm lithium) and oriented San Carlos olivine (∼2 ppm lithium) were juxtaposed. The lithium concentration along traverses across the run products was measured using both laser ablation as a source for a Varian 820-MS quadrupole mass spectrometer and a CAMECA 1270 secondary ion mass spectrometer. The CAMECA 1270 was also used to measure the lithium isotopic fractionation across olivine grains recovered from the experiments. The lithium isotopes were found to be fractionationed by many tens of permil in the diffusion boundary layer at the grain edges as a result of 6Li diffusing significantly faster than 7Li. The lithium concentration and isotopic fractionation data across the olivine recovered from the different experiments were modeled using calculations in which lithium was assumed to be of two distinct types - one being fast diffusing interstitial lithium, the other much less mobile lithium on a metal site. The two-site diffusion model involves a large number of independent parameters and we found that different choices of the parameters can produce very comparable fits to the lithium concentration profiles and associated isotopic fractionation. Because of this nonuniqueness we are able to determine only a range for the relative diffusivity of 6Li compared to 7Li. When the mass dependence of lithium diffusion is parameterized as D6Li /D7Li =(7 / 6) β , the isotope fractionation for diffusion along the a and c crystallographic direction of olivine can be fit by β = 0.4 ± 0

  9. Sound velocities of olivine at high pressures and temperatures and the composition of Earth's upper mantle

    NASA Astrophysics Data System (ADS)

    Zhang, Jin S.; Bass, Jay D.

    2016-09-01

    We present the elastic properties of San Carlos olivine up to P = 12.8(8) GPa and T = 1300(200) K using Brillouin spectroscopy with CO2 laser heating. A comparison of our results with the global seismic model AK135 yields average olivine content near 410 km depth of about 37% and 43% in a dry and wet (1.9 wt % H2O) upper mantle, respectively. These olivine contents are far less than in the pyrolite model. However, comparisons of our results with regional seismic models lead to very different conclusions. High olivine contents of up to 87% are implied by seismic models of the western U.S. and eastern Pacific regions. In contrast, we infer less than 35% olivine under the central Pacific. Strong variations of olivine content and upper mantle lithologies near the 410 km discontinuity are suggested by regional seismic models.

  10. The Atlantis Bank gabbro-suite was not a "normal" magma-chamber that produced basalts

    NASA Astrophysics Data System (ADS)

    Kvassnes, A. J.; Dick, H. J. B.; Grove, T. L.

    2003-04-01

    The differentiation of the basalts sampled at Atlantis II Fracture Zone, South-West Indian Ridge, is not the result of simple fractionation of gabbroic mineral-assemblages like those recovered from the adjacent Atlantis Bank and ODP Hole 735B. Large mineral data sets for the gabbros (Dick, et al 2002) are now available for analysis and comparison to spatially associated basalts. We have used Melts and pMelts (Ghiorso and Sack, 1995) to estimate the fractional crystallization trend gabbros from a primitive mantle melt or of the AII F.Z. MORB. Thermodynamic models (Grove et al (1992), Putirka (1999)) were also used to model the glasses hypothetical mafic and felsic mineral equilibrium-compositions. Our results show that while the basalts suggest 30-50% crystallization, the gabbros indicate 35-90% crystallization of a primary melt. It is therefore unlikely that the gabbros sampled from Atlantis Bank are the fossil magma-chambers that expelled melts that formed the spatially associated basalts. The models also show that the most primitive gabbros have elevated clinopyroxene Mg#s (Mg/(Mg+Fe)) relative to the coexisting plagioclase An%. This was unexpected, as the clinopyroxene frequently occurs as oikocrysts surrounding the plagioclase and encloses rounded olivine chadacrysts, indicating that the clinopyroxene precipitated late. Elthon (1992) noted the same problem for Cayman Trough gabbros; suggesting that this was the result of intermediate pressure fractionation. In our models, pressure does have some effect up to 5kbar, but is not enough to explain the discrepancy. We propose a model where melts are modified in a porous network or mush. Plagioclase-olivine networks form by accumulation of buoyant glomerocrysts and then work as filters as new melts pass through. Dissolution of the minerals would make the new melt appear to be more primitive with regards to increased Mg#s, as the dissolution happens fast without complete internal re-equilibration with the gabbro

  11. Diffusivity of hydrogen in iron-bearing olivine at 3 GPa

    NASA Astrophysics Data System (ADS)

    Demouchy, Sylvie; Thoraval, Catherine; Bolfan-Casanova, Nathalie; Manthilake, Geeth

    2016-11-01

    The kinetics of hydrogenation of dry iron-bearing olivine single crystals was determined by performing hydration experiments under hydrothermal conditions at high pressure. The experiments were performed in a multi-anvil press at 3 GPa, for a temperature range between 900 and 1200 °C and for various durations. The oxygen fugacity was buffered along Ni-NiO joint. Polarized Fourier transform infrared spectroscopy and recent empirical calibration were used to quantify the hydroxyl distributions in the samples along crystallographic axes after the experiments. The chemical diffusion coefficients are similar (barely slower) than in olivine hydrated at lower pressure (0.2 and 0.3 GPa) for the same diffusion mechanism. Under the given experimental conditions, the anisotropy of diffusion is the same as for proton-vacancy mechanism, with diffusion along the [0 0 1] axis faster than along the [1 0 0]. However, the anisotropy at 3 GPa is weaker compared to measurements at lower pressures and the analysis of concentration profiles using 3D models shows that an isotropic solution could also be relevant. Fits of the diffusion data to an Arrhenius law yield activation energies for the slightly faster [0 0 1] axis of the crystallographic axes around 198 ± 5 kJ mol-1, a value only slightly lower than the results from previous experimental studies for natural iron-bearing olivine hydrogenated at lower confining pressure. At 3 GPa, hydrogenation can be well approximated by a single mechanism controlled by coupled diffusion of protons and octahedral vacancies (di- and tri-valent ions). The diffusion rates are fast enough to alter hydrogen concentration within olivine in xenoliths ascending from the mantle or experiencing hydrogen-rich metasomatism events, but too slow to permit complete homogenization of hydrogen in olivine-rich rocks at kilometer scale in less than one My.

  12. Dehydration breakdown of antigorite and the formation of B-type olivine CPO

    NASA Astrophysics Data System (ADS)

    Nagaya, Takayoshi; Wallis, Simon R.; Kobayashi, Hiroaki; Michibayashi, Katsuyoshi; Mizukami, Tomoyuki; Seto, Yusuke; Miyake, Akira; Matsumoto, Megumi

    2014-02-01

    Peridotite formed by contact metamorphism and dehydration breakdown of an antigorite schist from the Happo area, central Japan shows a strong olivine crystallographic preferred orientation (Ol CPO). The lack of mesoscale deformation structures associated with the intrusion and the lack of microstructural evidence for plastic deformation of neoblastic grains suggest that olivine CPO in this area did not form as a result of solid-state deformation. Instead, the good correspondence between the original antigorite orientation and the orientation of the newly formed olivine implies the CPO formed by topotactic growth of the olivine after antigorite. Ol CPO is likely to develop by a similar process in subduction zone environments where foliated serpentinite is dragged down to depths where antigorite is no longer stable. The Happo Ol CPO has a strong a-axis concentration perpendicular to the lineation and within the foliation-commonly referred to as B-type Ol CPO. Seismic fast directions parallel to the ocean trench are observed in many convergent margins and are consistent with the presence of B-type Ol CPO in the mantle wedge of these regions. Experimental work has shown that B-type CPO can form by dislocation creep under hydrous conditions at relatively high stresses. There are, however, several discrepancies between the characteristics of natural and laboratory samples with B-type Ol CPO. (1) The formation conditions (stress and temperature) of some natural examples with B-type CPO fall outside those predicted by experiments. (2) In deformation experiments, slip in the crystallographic c-axis direction is important but has not been observed in natural examples of B-type CPO. (3) Experimental work suggests the presence of H2O and either high shear stress or relatively low temperatures are essential for the formation of B-type CPO. These conditions are most likely to be achieved close to subduction boundaries, but these regions are also associated with serpentinization

  13. Relation of the spectroscopic reflectance of olivine to mineral chemistry and some remote sensing implications.

    USGS Publications Warehouse

    King, T.V.V.; Ridley, W.I.

    1987-01-01

    Using high-resolution visible and near-infrared diffuse spectral reflectance, systematically investigates apparent wavelength shifts as a function of mineral chemistry in the Fe/Mg olivine series from Fo11 to Fo91. The study also shows that trace amounts of nickel can be spectrally detected in the olivine structure. Significant spectral variation as a function of grain size is also demonstrated, adding a further complication to the interpretation of remotely sensed data from olivine-rich surfaces. Some permutations of Fe-Mg-Ni relations in olivines are discussed as they apply to the interpretation of asteroid surfaces and other extraterrestrial bodies. -from Authors

  14. Partitioning of light lithophile elements during basalt eruptions on Earth and application to Martian shergottites

    NASA Astrophysics Data System (ADS)

    Edmonds, Marie

    2015-02-01

    An enigmatic record of light lithophile element (LLE) zoning in pyroxenes in basaltic shergottite meteorites, whereby LLE concentrations decrease dramatically from the cores to the rims, has been interpreted as being due to partitioning of LLE into a hydrous vapor during magma ascent to the surface on Mars. These trends are used as evidence that Martian basaltic melts are water-rich (McSween et al., 2001). Lithium and boron are light lithophile elements (LLE) that partition into volcanic minerals and into vapor from silicate melts, making them potential tracers of degassing processes during magma ascent to the surface of Earth and of other planets. While LLE degassing behavior is relatively well understood for silica-rich melts, where water and LLE concentrations are relatively high, very little data exists for LLE abundance, heterogeneity and degassing in basaltic melts. The lack of data hampers interpretation of the trends in the shergottite meteorites. Through a geochemical study of LLE, volatile and trace elements in olivine-hosted melt inclusions from Kilauea Volcano, Hawaii, it can be demonstrated that lithium behaves similarly to the light to middle rare Earth elements during melting, magma mixing and fractionation. Considerable heterogeneity in lithium and boron is inherited from mantle-derived primary melts, which is dominant over the fractionation and degassing signal. Lithium and boron are only very weakly volatile in basaltic melt erupted from Kilauea Volcano, with vapor-melt partition coefficients <0.1. Degassing of LLE is further inhibited at high temperatures. Pyroxene and associated melt inclusion LLE concentrations from a range of volcanoes are used to quantify lithium pyroxene-melt partition coefficients, which correlate negatively with melt H2O content, ranging from 0.13 at low water contents to <0.08 at H2O contents >4 wt%. The observed terrestrial LLE partitioning behavior is extrapolated to Martian primitive melts through modeling. The zoning

  15. Mineralogy and Petrology of Amoeboid Olivine Inclusions in CO3 Chondrites: Relationship to Parent-Body Aqueous Alteration

    NASA Technical Reports Server (NTRS)

    Chizmadia, Lysa J.; Rubin, Alan E.; Wasson, John T.

    2003-01-01

    Petrographic and mineralogic studies of amoeboid olivine inclusions (AOIs) in CO3 carbonaceous chondrites reveal that they are sensitive indicators of parent-body aqueous and thermal alteration. As the petrologic subtype increases from 3.0 to 3.8, forsteritic olivine (Fa(sub 0-1)) is systematically converted into ferroan olivine (Fa(sub 60-75)). We infer that the Fe, Si and O entered the assemblage along grain boundaries, forming ferroan olivine that filled fractures and voids. As temperatures increased, Fe(+2) from the new olivine exchanged with Mg(+2) from the original AOI to form diffusive haloes around low-FeO cores. Cations of Mn(+2), Ca(+2) and Cr(+3) were also mobilized. The systematic changes in AOI textures and olivine compositional distributions can be used to refine the classification of CO3 chondrites into subtypes. In subtype 3.0, olivine occurs as small forsterite grains (Fa(sub 0-1)), free of ferroan olivine. In petrologic subtype 3.2, narrow veins of FeO-rich olivine have formed at forsterite grain boundaries. With increasing alteration, these veins thicken to form zones of ferroan olivine at the outside AOI margin and within the AOI interior. By subtype 3.7, there is a fairly broad olivine compositional distribution in the range Fa(sub 63-70), and by subtype 3.8, no forsterite remains and the high-Fa peak has narrowed, Fa(sub 64-67). Even at this stage, there is incomplete equilibration in the chondrite as a whole (e.g., data for coarse olivine grains in Isna (CO3.8) chondrules and lithic clasts show a peak at Fa(sub39)). We infer that the mineral changes in A01 identified in the low petrologic types required aqueous or hydrothermal fluids whereas those in subtypes greater than or equal to 3.3 largely reflect diffusive exchange within and between mineral grains without the aid of fluids.

  16. Alkali metal ionization detector

    DOEpatents

    Bauerle, James E.; Reed, William H.; Berkey, Edgar

    1978-01-01

    Variations in the conventional filament and collector electrodes of an alkali metal ionization detector, including the substitution of helical electrode configurations for either the conventional wire filament or flat plate collector; or, the substitution of a plurality of discrete filament electrodes providing an in situ capability for transferring from an operationally defective filament electrode to a previously unused filament electrode without removing the alkali metal ionization detector from the monitored environment. In particular, the helical collector arrangement which is coaxially disposed about the filament electrode, i.e. the thermal ionizer, provides an improved collection of positive ions developed by the filament electrode. The helical filament design, on the other hand, provides the advantage of an increased surface area for ionization of alkali metal-bearing species in a monitored gas environment as well as providing a relatively strong electric field for collecting the ions at the collector electrode about which the helical filament electrode is coaxially positioned. Alternatively, both the filament and collector electrodes can be helical. Furthermore, the operation of the conventional alkali metal ionization detector as a leak detector can be simplified as to cost and complexity, by operating the detector at a reduced collector potential while maintaining the sensitivity of the alkali metal ionization detector adequate for the relatively low concentration of alkali vapor and aerosol typically encountered in leak detection applications.

  17. EXTINGUISHMENT OF ALKALI METAL FIRES

    DTIC Science & Technology

    was found to be effective on low temperature (1000F) fires and was useful on alkali metal fires on or under insulation. Organic liquids were not...particularly effective on alkali metal fires . A section is presented on a typical alkali metal system which might be used to generate electrical power in space.

  18. Basaltic volcanism - The importance of planet size

    NASA Technical Reports Server (NTRS)

    Walker, D.; Stolper, E. M.; Hays, J. F.

    1979-01-01

    The volumetrically abundant basalts on the earth, its moon, and the eucrite parent planet all have chemical compositions that are controlled to a large extent by dry, low-pressure, crystal-liquid equilibria. Since this generalization is valid for these three planetary bodies, we infer that it may also apply to the other unsampled terrestrial planets. Other characteristics of basaltic volcanism show variations which appear to be related to planet size: the eruption temperatures, degrees of fractionation, and chemical variety of basalts and the endurance of basaltic volcanism all increase with planet size. Although the processes responsible for chemical differences between basalt suites are known, no simple systematization of the chemical differences between basalts from planet to planet has emerged.

  19. Calcium Sulfate in Atacama Desert Basalt: A Possible Analog for Bright Material in Adirondack Basalt, Gusev Crater

    NASA Technical Reports Server (NTRS)

    Sutter, B.; Golden, D. C.; Amundson, R.; Chong-Diaz, G.; Ming, D. W.

    2007-01-01

    The Atacama Desert in northern Chile is one of the driest deserts on Earth (< 2mm/y). The hyper-arid conditions allow extraordinary accumulations of sulfates, chlorides, and nitrates in Atacama soils. Examining salt accumulations in the Atacama may assist understanding salt accumulations on Mars. Recent work examining sulfate soils on basalt parent material observed white material in the interior vesicles of surface basalt. This is strikingly similar to the bright-white material present in veins and vesicles of the Adirondack basalt rocks at Gusev Crater which are presumed to consist of S, Cl, and/or Br. The abundance of soil gypsum/anhydrite in the area of the Atacama basalt suggested that the white material consisted of calcium sulfate (Ca-SO4) which was later confirmed by SEM/EDS analysis. This work examines the Ca-SO4 of Atacama basalt in an effort to provide insight into the possible nature of the bright material in the Adirondack basalt of Gusev Crater. The objectives of this work are to (i) discuss variations in Ca-SO4 crystal morphology in the vesicles and (ii) examine the Ca-SO4 interaction(s) with the basalt interior.

  20. Diffusion of hydrogen in olivine: Implications for water in the mantle

    NASA Astrophysics Data System (ADS)

    Mackwell, Stephen J.; Kohlstedt, David L.

    1990-04-01

    To investigate the kinetics of diffusion of hydrogen in olivine, single crystals from San Carlos in Arizona have been annealed at temperatures between 800° and 1000°C under hydrothermal conditions at a confining pressure of 300 MPa. The hydrogen diffusivities were determined for the [100], [010], and [001] directions from concentration profiles for hydroxyl in the samples. These profiles were obtained from infrared spectra taken at 100-μm intervals across a thin slice which was cut from the central portion of each annealed crystal. The rate of diffusion is anisotropic, with fastest transport along the [100] axis and slowest along the [010] axis. The fit of the data to an Arrhenius law for diffusion parallel to [100] yields an activation enthalpy of 130±30 kJ/mol with a preexponential term of (6±3)×10-5 m2 s-1. For diffusion parallel to [001], as there are insufficient data to calculate the activation enthalpy for diffusion, we used the same value as that for diffusion parallel to [100] and determined a preexponential term of (5±4)×10-6 m2 s-1. The diffusion rate parallel to [010] is about 1 order of magnitude slower than along [001]. The measured diffusivities are large enough that the hydrogen content of olivine grains which are millimeters in diameter will adjust to changing environmental conditions in time scales of hours at temperatures as low as 800°C. As xenoliths ascending from the mantle remain at high temperatures (i.e., >1000°C) but experience a rapid decrease in pressure, and hence hydrogen fugacity, olivine grains may dehydrate during ascent. By comparison, slow rates of carbon diffusion (Tingle et al., 1988) suggest that carbon will not be lost from olivine during ascent. Thus, low hydrogen contents within olivine and within fluid inclusions in olivine cannot be taken as support for low water contents in the mantle.

  1. Development of olivine crystallographic preferred orientation in response to strain-induced fabric geometry

    NASA Astrophysics Data System (ADS)

    Chatzaras, Vasileios; Kruckenberg, Seth C.; Cohen, Shaina M.; Medaris, L. Gordon, Jr.; Withers, Anthony C.; Bagley, Brian

    2016-04-01

    The effect of finite strain ellipsoid geometry on crystallographic preferred orientation (CPO) is well known for crustal minerals (e.g., quartz, calcite, biotite, and hornblende). In the upper mantle, however, it remains poorly constrained how strain and fabric may affect olivine CPO. We present data from a suite of 40 spinel peridotite xenoliths from Marie Byrd Land (west Antarctica), which support an interpretation that fabric geometry rather than deformation conditions control the development of olivine CPO. We use X-ray computed tomography (XRCT) to quantitatively determine spinel fabric (orientation and geometry). Olivine CPOs, determined by Electron Backscattered Diffraction (EBSD), are plotted with respect to the XRCT-derived spinel foliation and lineation; this approach allows for the accurate, and unbiased, identification of CPO symmetries and types in mantle xenoliths. The combined XRCT and EBSD data show that the xenoliths are characterized by a range of fabric geometries (from oblate to prolate) and olivine CPO patterns; we recognize the A-type, axial-[010], axial-[100], and B-type patterns. The mantle xenoliths equilibrated at temperatures 779-1198 oC, as determined by 2-Px geothermometry. Using a geotherm consistent with the stability of spinel in all xenoliths, the range of equilibration temperatures occurs at depths between 39 and 72 km. Olivine recrystallized grain size piezometry reveals differential stresses ranging 2-60 MPa. Analysis of low-angle misorientation axes show a wide range in the distribution of rotation axes, with dominant {0kl}[100] slip. We use Fourier Transform Infrared (FTIR) spectroscopy to estimate the water content in the xenolith with the B-type CPO pattern. FTIR analysis shows that the equilibrium H concentration in olivine is low (4-13 ppm H2O). Combining these data, we observe that olivine CPO symmetry is controlled neither by the deformation conditions (stress, temperature, pressure, water content) for the range of

  2. 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

  3. Comparing olivine single crystal and polycrystal rheology: evidence for supplementary accommodation mechanisms at grain boundaries

    NASA Astrophysics Data System (ADS)

    Bollinger, C.; Merkel, S.; Raterron, P.; Castelnau, O.; Detrez, F.

    2013-12-01

    Rheology in the Earth's upper-mantle is mostly constrained by the plastic properties of olivine. Over recent years, several groups have been carrying out deformation experiments on single crystals and polycrystals of olivine at upper mantle pressure (P) and temperature (T). Yet, the rheology of olivine at mantle conditions is still not well constrained. We carried out deformation experiments on San Carlos olivine polycrystals, at P and T ranging from 3 to 8 GPa and 1373 to 1673 K, respectively, and at strain rates ranging from 10-6 to 10-4 s-1, using the D-DIA apparatus installed at the NSLS X17B2 beamline (NY, USA). The deformation rates of the polycrystals are compared to those of single crystals oriented along the soft orientations [110]c, [011]c, [101]c which activate the easiest slip systems (Raterron et al., 2012). This comparison suggests that, in olivine polycrystals deforming in the dislocation creep regime, other relaxation mechanisms need to be considered to account for the observed polycrystal strain rates. This highlights the importance of supplementary mechanisms, such as those occurring at grain boundaries, to properly model olivine aggregates plasticity.

  4. Olivine Dissolution in Seawater: Implications for CO2 Sequestration through Enhanced Weathering in Coastal Environments

    PubMed Central

    2017-01-01

    Enhanced weathering of (ultra)basic silicate rocks such as olivine-rich dunite has been proposed as a large-scale climate engineering approach. When implemented in coastal environments, olivine weathering is expected to increase seawater alkalinity, thus resulting in additional CO2 uptake from the atmosphere. However, the mechanisms of marine olivine weathering and its effect on seawater–carbonate chemistry remain poorly understood. Here, we present results from batch reaction experiments, in which forsteritic olivine was subjected to rotational agitation in different seawater media for periods of days to months. Olivine dissolution caused a significant increase in alkalinity of the seawater with a consequent DIC increase due to CO2 invasion, thus confirming viability of the basic concept of enhanced silicate weathering. However, our experiments also identified several important challenges with respect to the detailed quantification of the CO2 sequestration efficiency under field conditions, which include nonstoichiometric dissolution, potential pore water saturation in the seabed, and the potential occurrence of secondary reactions. Before enhanced weathering of olivine in coastal environments can be considered an option for realizing negative CO2 emissions for climate mitigation purposes, these aspects need further experimental assessment. PMID:28281750

  5. B-type olivine fabric induced by low temperature dissolution creep during serpentinization and deformation in mantle wedge

    NASA Astrophysics Data System (ADS)

    Liu, Wenlong; Zhang, Junfeng; Barou, Fabrice

    2018-01-01

    The B-type olivine fabric (i.e., the [010] axes subnormal to foliation and the [001] axes subparallel to the lineation) has been regarded as an important olivine fabric for interpreting global trench-parallel S-wave polarization in fore-arc regions. However, strong serpentinization and cold temperature environment in the mantle wedge should inhibit development of the B-type olivine fabric that requires high temperature to activate solid-state plastic deformation. Here we report fabrics of olivine and antigorite generated at low temperatures (300-370 °C) during serpentinization in a fossil mantle wedge of the Val Malenco area, Central Alps. Olivine in the serpentine matrix develops a pronounced B-type fabric, while antigorite in the same matrix displays a strong crystallographic preferred orientation (CPO) with the (001) planes and the [010] axes subparallel to foliation and lineation, respectively. The following evidence leads to the conclusion that the B-type olivine fabric results from dissolution creep assisted by grain boundary sliding (GBS) and grain rotation, rather than solid-state plastic deformation: (1) serpentinization took place at low temperatures and a fluid-enriched environment, ideal for dissolution-precipitation creep; (2) the voids and zigzag boundaries along the interface between antigorite and olivine suggest a fluid dissolution reaction; (3) the primary coarse olivine develops a nearly random fabric, indicating the B-type fabrics in the fine-grained olivine may not be inherited fabrics. These results document for the first time the B-type olivine CPO formed by dissolution creep at low temperatures during serpentinization and provide a mechanism to reconcile petrofabric observations with geophysical observations of trench parallel fast S-wave seismic anisotropy in fore-arc mantle wedge regions.

  6. High-silica glass inclusions in olivine of Luna-24 samples

    NASA Technical Reports Server (NTRS)

    Roedder, E.; Weiblen, P. W.

    1977-01-01

    Optical examination of nine polished grain mounts of Luna-24 drill-core material (0.09-0.50 mm size) revealed melt inclusions in olivine crystals. Two inclusions consist of clear glass with exceptionally high Si, yet contain no visible daughter minerals and have had no reaction effects with the olivine walls. Their compositions (one has SiO2 93.8, Al2O3 1.51, FeO 2.32, MgO 1.61, CaO 0.06, Na2O less than 0.05, K2O 0.11, total 99.41%; the other is similar) are unique and quite unlike the high-Si high-K melt of granitic composition that is found as inclusions in late-stage minerals of these (and the Apollo) samples, from silicate liquid immiscibility. The host olivines are Fo73 and Fo51. The origin of the melt in the inclusions and the lack of reaction effects are perplexing unsolved problems.

  7. Geochemical and Petrologic Constraints on the Source of Eocene Volcanism at Mole Hill, Rockingham County, VA

    NASA Astrophysics Data System (ADS)

    Johnson, E. A.; Beard, J. S.

    2010-12-01

    -78). Groundmass olivine is ˜Fo70. Spinel xenocryst compositions fall within the hercynite-spinel series, have Cr#<1, and lack compositional zoning within individual grains, although a range of compositions are present between grains. The compositional zoning observed in olivine and clinopyroxene xenocrysts is consistent with entrainment and partial reequilibration with the alkali basalt. Sieve-textured rims on clinopyroxene xenocrysts and phenocrysts may have formed during rapid ascent to the surface. The xenocrystic assemblage is dominated by Al-rich, Cr-poor augite and may represent a metasomatized mantle source. The presence of spinel xenocrysts indicates at least some of the mantle xenocrysts entrained in the Mole Hill basalt originated within the spinel stability field at about 30-70 km depth. Preliminary models from the TEENA seismic array (Benoit and Long 2009, Eos U53A-0053) estimate a crustal thickness of ˜40 km below the Shenandoah Valley which is consistent with the presence of shallow spinel-bearing lithospheric mantle.

  8. Effect of alkali lignins with different molecular weights from alkali pretreated rice straw hydrolyzate on enzymatic hydrolysis.

    PubMed

    Li, Yun; Qi, Benkun; Luo, Jianquan; Wan, Yinhua

    2016-01-01

    This study investigated the effect of alkali lignins with different molecular weights on enzymatic hydrolysis of lignocellulose. Different alkali lignins fractions, which were obtained from cascade ultrafiltration, were added into the dilute acid pretreated (DAP) and alkali pretreated (AP) rice straws respectively during enzymatic hydrolysis. The results showed that the addition of alkali lignins enhanced the hydrolysis and the enhancement for hydrolysis increased with increasing molecular weights of alkali lignins, with maximum enhancement being 28.69% for DAP and 20.05% for AP, respectively. The enhancement was partly attributed to the improved cellulase activity, and filter paper activity increased by 18.03% when adding lignin with highest molecular weight. It was found that the enhancement of enzymatic hydrolysis was correlated with the adsorption affinity of cellulase on alkali lignins, and the difference in surface charge and hydrophobicity of alkali lignins were responsible for the difference in affinity between cellulase and lignins. Copyright © 2015 Elsevier Ltd. All rights reserved.

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

    NASA Astrophysics Data System (ADS)

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

    2017-12-01

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

  10. The Effect of Trace H2O on the Mechanisms of the Olivine-Ringwoodite Transformation

    NASA Astrophysics Data System (ADS)

    Sharp, T. G.; Rieck, K. D.; Hu, J.; Du Frane, W. L.

    2011-12-01

    The existence of metastable olivine has been inferred as a possible trigger of deep focus earthquakes. Because hydrogen increases olivine-ringwoodite transformation rates, the existence of metastable olivine in the transition would require the subduction of very dry olivine. Our previous work has shown that for San Carlos olivine spheres, hydrated in a piston cylinder with 75 ppm H2O and 300 ppm D2O, ringwoodite-rim growth rates are greatly enhanced relative to anhydrous samples (Du Frane2010 and Diedrich et al, 2009). In anhydrous samples, rim-growth rates decrease with time as elastic strain builds up in the system, eventually stopping the reaction. As strain increases, wadsleyite forms, rather than or in addition to ringwoodite. In hydrous samples, hydrogen partitions to the ringwoodite growth rim, hydrolytically weakening it, and preventing the build up of elastic strain energy. Eventually, elastic strain energy may build up in slightly hydrous samples if the hydrogen content of the rim decreases sufficiently. Here we investigate the transformation mechanisms in the same San Carlos olivine samples, hydrated to 75 and 300 ppm H2O and D2O and transformed at 18 GPa. A 75-ppm-H2O sample run at 1100°C for 40 minutes shows a complex mixture of reaction textures. Optical microscopy and Raman spectroscopy show that the ringwoodite rims are nearly pure ringwoodite with minor amounts of wadsleyite. Scanning electron microscopy and transmission electron microscopy on a Focused Ion Beam slices of this sample show that the outermost rim is uniform, relatively course grained and defect free ringwoodite. This suggests limited nucleation at the sample-capsule interface and fairly rapid incoherent growth. The inner rim consists of a complex mixture of olivine and ringwoodite in which most of the ringwoodite has no crystallographic relationship to the host olivine and therefore represents incoherent nucleation and growth. Coherent ringwoodite lamellae are also present in the

  11. Cellular Precipitates Of Iron Oxide in Olivine in a Stratospheric Interplanetary Dust Particle

    NASA Technical Reports Server (NTRS)

    Rietmeijer, Frans J. M.

    1996-01-01

    The petrology of a massive olivine-sulphide interplanetary dust particle shows melting of Fe,Ni-sulphide plus complete loss of sulphur and subsequent quenching to a mixture of iron-oxides and Fe,Ni-metal. Oxidation of the fayalite component in olivine produced maghemite discs and cellular intergrowths with olivine and rare andradite-rich garnet. Cellular reactions require no long-range solid-state diffusion and are kinetically favourable during pyrometamorphic oxidation. Local melting of the cellular intergrowths resulted in three dimensional symplectic textures. Dynamic pyrometamorphism of this asteroidal particle occurred at approx. 1100 C during atmospheric entry flash (5-15 s) heating.

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

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

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

  13. Viscous anisotropy of textured olivine aggregates: 2. Micromechanical model

    NASA Astrophysics Data System (ADS)

    Hansen, Lars N.; Conrad, Clinton P.; Boneh, Yuval; Skemer, Philip; Warren, Jessica M.; Kohlstedt, David L.

    2016-10-01

    The significant viscous anisotropy that results from crystallographic alignment (texture) of olivine grains in deformed upper mantle rocks strongly influences a large variety of geodynamic processes. Our ability to explore the effects of anisotropic viscosity in simulations of these processes requires a mechanical model that can predict the magnitude of anisotropy and its evolution. Unfortunately, existing models of olivine textural evolution and viscous anisotropy are calibrated for relatively small deformations and simple strain paths, making them less general than desired for many large-scale geodynamic scenarios. Here we develop a new set of micromechanical models to describe the mechanical behavior and textural evolution of olivine through a large range of strains and complex strain histories. For the mechanical behavior, we explore two extreme scenarios, one in which each grain experiences the same stress tensor (Sachs model) and one in which each grain undergoes a strain rate as close as possible to the macroscopic strain rate (pseudo-Taylor model). For the textural evolution, we develop a new model in which the director method is used to control the rate of grain rotation and the available slip systems in olivine are used to control the axis of rotation. Only recently has enough laboratory data on the deformation of olivine become available to calibrate these models. We use these new data to conduct inversions for the best parameters to characterize both the mechanical and textural evolution models. These inversions demonstrate that the calibrated pseudo-Taylor model best reproduces the mechanical observations. Additionally, the pseudo-Taylor textural evolution model can reasonably reproduce the observed texture strength, shape, and orientation after large and complex deformations. A quantitative comparison between our calibrated models and previously published models reveals that our new models excel in predicting the magnitude of viscous anisotropy and

  14. Water sensitivity of the seismic properties of polycrystalline olivine

    NASA Astrophysics Data System (ADS)

    Cline, C. J., II; Jackson, I.; Faul, U.; Berry, A.

    2016-12-01

    Fully synthetic solgel-derived Fo90 olivine specimens have been fabricated with varying concentrations of hydroxyl, chemically bound as doubly protonated Si vacancies associated with nearby Ti/Mg substitution (the `Ti-clinohumite' defect). The `water' contents of three such specimens hot-pressed within welded Pt capsules are controlled by the amount of added TiO2-dopant and ranged between 176 and 802 ppm Ti/Si, providing concentrations of bound hydrogen ranging between 330 and 1150 ppm H/Si respectively. These sol-gel derived specimens, along with another natural Ti-bearing specimen hot-pressed from powder produced by grinding hand-picked single crystals of San Carlos olivine, were then each subsequently wrapped in Pt and interrogated under water-undersaturated conditions via forced torsional oscillation. Testing was conducted at seismic periods of 1 - 1000 s and 200 MPa confining pressure during slow staged cooling from 1200 to 25 °C. All Ti-doped hydrous specimens tested, including the San Carlos olivine specimen, show high temperature background behavior, involving monotonically increasing levels of dissipation and decreasing values of shear modulus with increasing oscillation period and increasing temperature. Comparison of the mechanical behavior observed in these water-undersaturated specimens to that for a similarly fabricated dry Ti-bearing olivine specimen shows a striking contrast, with much more dissipation and lower modulus observed in the hydrous specimens, but with limited sensitivity of seismic properties to the total water content among the hydrous specimens in the series. Further experiments in progress on Pt-sleeved, dry, undoped Fo90 are designed to clarify further the sensitivity of the seismic properties to water content and possibly oxygen fugacity.

  15. Size effects resolve discrepancies in 40 years of work on low-temperature plasticity in olivine

    PubMed Central

    Kumamoto, Kathryn M.; Thom, Christopher A.; Wallis, David; Hansen, Lars N.; Armstrong, David E. J.; Warren, Jessica M.; Goldsby, David L.; Wilkinson, Angus J.

    2017-01-01

    The strength of olivine at low temperatures and high stresses in Earth’s lithospheric mantle exerts a critical control on many geodynamic processes, including lithospheric flexure and the formation of plate boundaries. Unfortunately, laboratory-derived values of the strength of olivine at lithospheric conditions are highly variable and significantly disagree with those inferred from geophysical observations. We demonstrate via nanoindentation that the strength of olivine depends on the length scale of deformation, with experiments on smaller volumes of material exhibiting larger yield stresses. This “size effect” resolves discrepancies among previous measurements of olivine strength using other techniques. It also corroborates the most recent flow law for olivine, which proposes a much weaker lithospheric mantle than previously estimated, thus bringing experimental measurements into closer alignment with geophysical constraints. Further implications include an increased difficulty of activating plasticity in cold, fine-grained shear zones and an impact on the evolution of fault surface roughness due to the size-dependent deformation of nanometer- to micrometer-sized asperities. PMID:28924611

  16. Reconsideration of evolutionary model of the Hawaiian-type volcano: 40Ar/39Ar ages for lavas from deep interior of Oahu Island and alkali basalts from the North Arch volcanic field

    NASA Astrophysics Data System (ADS)

    Uto, K.; Ishizuka, O.; Garcia, M. O.; Clague, D. A.; Naka, J.

    2002-12-01

    from the place it was born. This may suggest the dimension of Hawaiian plume if it had been fixed to the earth, or may indicate the some temporal swing of the plume. North Arch volcanic field is a wide-spread flat lava flow field of extremely silica undersaturated alkali basalts existing about 200 km north from the Hawaiian volcanic chain. Six lavas taken by {\\SHINKAI6500} and four samples dredged by USGS are dated. Ages are continuously ranging from 1.4 to 0.5 Ma, suggesting that the volcanism continued at least one million years contemporaneously with rejuvinated-stage volcanism on the islands of Oahu, Niihau, Kauai and Molokai. Chemical compositions of North-Arch lavas are within the variation of these rejuvinated-stage alkali basalts. The similarities in ages and chemistry question the origin of rejuvinated-stage volcanism. These lavas may not be peripheral products of Hawaiian plume, but represent marginal volcanoes of much larger North Arch volcanic field.

  17. Purification of alkali metal nitrates

    DOEpatents

    Fiorucci, Louis C.; Gregory, Kevin M.

    1985-05-14

    A process is disclosed for removing heavy metal contaminants from impure alkali metal nitrates containing them. The process comprises mixing the impure nitrates with sufficient water to form a concentrated aqueous solution of the impure nitrates, adjusting the pH of the resulting solution to within the range of between about 2 and about 7, adding sufficient reducing agent to react with heavy metal contaminants within said solution, adjusting the pH of the solution containing reducing agent to effect precipitation of heavy metal impurities and separating the solid impurities from the resulting purified aqueous solution of alkali metal nitrates. The resulting purified solution of alkali metal nitrates may be heated to evaporate water therefrom to produce purified molten alkali metal nitrate suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of alkali metal nitrates.

  18. Pyroxenes and olivines: Structural implications of shock-wave data for high pressure phases

    NASA Technical Reports Server (NTRS)

    Jeanloz, R.; Ahrens, T. J.

    1975-01-01

    The nature of the shock-induced, high-pressure phases of olivine and pyroxene rocks is examined in the light of data for the densities of a new class of perovskite-related silicate structures. Also examined are some new Hugoniot and release adiabat data for bronzite. Reexamining available shock data for magnesian pyroxenes and olivines leads to the conclusion that they define a mixed phase (or disequilibrium) region to about the 100 GPa range, related to the kinetics of phase transformation in these silicates. By recognizing this point, certain discrepancies in previous interpretations of shock data can be explained. A set of theoretical Hugonoits for pyroxene and olivine stoichiometry, perovskite-bearing assemblages was constructed based on their properties deduced from high-pressure work, showing that the shock data is compatible with transformations to perovskites in the 45-7GPa region. Finally, the shock data indicate very similar properties for olivine and pyroxene at high pressures making them both equally likely candidates for the lower mantle.

  19. Mobility and fluxes of major, minor and trace metals during basalt weathering and groundwater transport at Mt. Etna volcano (Sicily)

    NASA Astrophysics Data System (ADS)

    Aiuppa, Alessandro; Allard, Patrick; D'Alessandro, Walter; Michel, Agnes; Parello, Francesco; Treuil, Michel; Valenza, Mariano

    2000-06-01

    The concentrations and fluxes of major, minor and trace metals were determined in 53 samples of groundwaters from around Mt Etna, in order to evaluate the conditions and extent of alkali basalt weathering by waters enriched in magma-derived CO 2 and the contribution of aqueous transport to the overall metal discharge of the volcano. We show that gaseous input of magmatic volatile metals into the Etnean aquifer is small or negligible, being limited by cooling of the rising fluids. Basalt leaching by weakly acidic, CO 2-charged water is the overwhelming source of metals and appears to be more extensive in two sectors of the S-SW (Paternò) and E (Zafferana) volcano flanks, where out flowing groundwaters are the richest in metals and bicarbonate of magmatic origin. Thermodynamic modeling of the results allows to evaluate the relative mobility and chemical speciation of various elements during their partitioning between solid and liquid phases through the weathering process. The facts that rock-forming minerals and groundmass dissolve at different rates and secondary minerals are formed are taken into account. At Mt. Etna, poorly mobile elements (Al, Th, Fe) are preferentially retained in the solid residue of weathering, while alkalis, alkaline earth and oxo-anion-forming elements (As, Se, Sb, Mo) are more mobile and released to the aqueous system. Transition metals display an intermediate behavior and are strongly dependent on either the redox conditions (Mn, Cr, V) or solid surface-related processes (V, Zn, Cu). The fluxes of metals discharged by the volcanic aquifer of Etna range from 7.0 × 10 -3 t/a (Th) to 7.3 × 10 4 t/a (Na). They are comparable in magnitude to the summit crater plume emissions for a series of elements (Na, K, Ca, Mg, U, V, Li) with lithophile affinity, but are minor for volatile elements. Basalt weathering at Mt Etna also consumes about 2.1 × 10 5 t/a of magma-derived carbon dioxide, equivalent to ca. 7% of contemporaneous crater plume

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

    NASA Astrophysics Data System (ADS)

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

    2016-12-01

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