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Abstract— We present here ion microprobe analyses of rare earth and other selected trace and minor elements in pyroxenes of shergottite Queen Alexandra Range 94201 and lunar basalt 15555. Pyroxene zonation patterns record the crystallization histories of these two basaltic samples from Mars and the Moon, respectively, and allow a comparison of mafic melt evolution on these two planetary bodies. Elemental abundances and trends in pyroxenes of these two rocks indicate that their minerals formed by continuous, closed system fractional crystallization of their respective parent melts. This further supports the idea that QUE 94201 closely represents the composition of a true Martian basaltic melt (McSween et al., 1996). The main differences in pyroxene elemental zonation patterns in these two objects are attributed to earlier crystallization of whitlockite in QUE 94201 (i.e., before the Fe-rich pyroxenes) than in 15555 (after the Fe-rich pyroxenes). The size of Eu anomalies in pyroxenes of QUE 94201 is intermediate between that in pyroxenes of 15555 and the other shergottites and may imply that fO2 conditions during crystallization of this Martian basalt were significantly more reducing than for other shergottites, although not quite as reducing as for lunar basalts. Cerium anomalies appear to be less prevalent in pyroxenes of QUE 94201 than other Antarctic shergottites and could be indicative of lesser degree of weathering in the Antarctic. 相似文献
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M. WADHWA R. C. F. LENTZ H. Y. McSWEEN G. CROZAZ 《Meteoritics & planetary science》2001,36(2):195-208
Abstract— We present the results of a combined mineralogic‐petrologic and ion microprobe study of two martian meteorites recently recovered in the Lybian Sahara, Dar al Gani 476 (DaG 476) and Dar al Gani 489 (DaG 489). Having resided in a hot desert environment for an extended time, DaG 476 and DaG 489 were subjected to terrestrial weathering that significantly altered their chemical composition. In particular, analyses of some of the silicates show light rare earth element (LREE)‐enrichment resulting from terrestrial alteration. In situ measurement of trace element abundances in minerals allows us to identify areas unaffected by this contamination and, thereby, to infer the petrogenesis of these meteorites. No significant compositional differences between DaG 476 and DaG 489 were found, supporting the hypothesis that they belong to the same fall. These meteorites have characteristics in common with both basaltic and lherzolitic shergottites, possibly suggesting spatial and petrogenetic associations of these two types of lithologies on Mars. However, the compositions of Fe‐Ti oxides and the size of Eu anomalies in the earliest‐formed pyroxenes indicate that the two Saharan meteorites probably experienced more reducing crystallization conditions than other shergottites (with the exception of Queen Alexandra Range (QUE) 94201). As is the case for other shergottites, trace element microdistributions in minerals of the DaG martian meteorites indicate that closed‐system crystal fractionation from a LREE‐depleted parent magma dominated their crystallization history. Furthermore, rare earth element abundances in the orthopyroxene megacrysts are consistent with their origin as xenocrysts rather than phenocrysts. 相似文献
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Christine FLOSS Ghislaine CROZAZ Brad JOLLIFF Gretchen BENEDIX Shannon COLTON 《Meteoritics & planetary science》2008,43(4):657-674
Abstract— We have measured the trace element compositions of individual plagioclase, pyroxene, and olivine grains in 6 different winonaites that span the range of textures and mineralogies observed in these meteorites. Textural evidence in these meteorites, including the presence of a plagioclase/clinopyroxene‐rich lithology and coarse‐grained olivine lithologies, suggests that they may have experienced some silicate partial melting. However, trace element distributions in these lithologies do not show any clear signatures for such an event. Pyroxene trace element compositions do exhibit systematic trends, with abundances generally lowest in Pontlyfni and highest in Winona. The fact that the same trends are present for both incompatible and compatible trace elements suggests, however, that the systematics are more likely the result of equilibration of minerals with initially heterogeneous and distinct compositions, rather than partial melting of a compositionally homogeneous precursor. The winonaites have experienced brecciation and mixing of lithologies, followed by varying degrees of thermal metamorphism on their parent body. These factors probably account for the variable bulk rare earth element (REE) patterns noted for these meteorites and may have led to re‐equilibration of trace elements in different lithologies. 相似文献
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Abstract— Electron and ion microprobe measurements of major, minor, and trace element concentrations were made in individual grains of pyroxene, plagioclase, and Ca phosphates in Pomozdino and Peramiho, two eucrites previously classified as anomalous. Although Pomozdino pyroxene is highly magnesian, minor and trace element concentrations in both pyroxene and plagioclase of this meteorite are similar to those in other noncumulate eucrites. High incompatible element concentrations (similar to those in Stannern) coupled with mg# typical of cumulate eucrites confirm the anomalous character of this meteorite but do not allow us to distinguish unequivocally between different possible modes of origin. Peramiho has mg# and trace element concentrations similar to main group eucrites, indicating that this meteorite most probably belongs to this group. A previously reported low incompatible element concentration for Peramiho may be due to a sampling problem. 相似文献
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Abstract— This paper explores the possible origin of the light rare earth element (LREE) enrichments observed in some ureilites, a question that has both petrogenetic and chronologic implications for this group of achondritic meteorites. Rare earth element and other selected elemental abundances were measured in situ in 14 thin sections representing 11 different ureilites. The spatial microdistributions of REEs in C‐rich matrix areas of the three ureilites with the most striking V‐shaped whole‐rock REE patterns (Kenna, Goalpara, and Novo Urei) were investigated using the ion imaging capability of the ion microprobe. All olivines and clinopyroxenes measured have LREE‐depleted patterns with little variation in REE abundances, despite large differences in their major element compositions from ureilite to ureilite. Furthermore, we searched for but did not find any minor mineral phases that carry LREEs. The only exception is one Ti‐rich area (～20μm) in Lewis Cliff (LEW) 85400 with a major element composition similar to that of titanite; REE abundances in this area are high, ranging from La ? 400 × CI to Lu ? 40 × CI. In contrast, all ion microprobe analyses of C‐rich matrix in Kenna, Goalpara, and Novo Urei revealed large LREE enrichments. In addition, C‐rich matrix areas in the three polymict ureilites, Elephant Moraine (EET) 83309, EET 87720, and North Haig, which have less pronounced V‐shaped whole‐rock REE patterns, show smaller but distinct LREE‐enrichments. The C‐rich matrix in Antarctic ureilites tends to have much lower LREE concentrations than the matrix in non‐Antarctic ureilites. There is no obvious association of the LREEs with other major or minor elements in the C‐rich areas. Ion images further show that the LREE enrichments are homogeneously distributed on a microscale in most C‐rich matrix areas of Kenna, Goalpara, and Novo Urei. These observations suggest that the LREEs in ureilites most probably are absorbed on the surface of fine‐grained amorphous graphite in the C‐rich matrix. It is unlikely that the LREE enrichments are due to shock melts or are the products of metasomatism on the ureilite parent body. We favor LREE introduction by terrestrial contamination. 相似文献
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Meenakshi WADHWA Ernst K. ZINNER Ghislaine CROZAZ 《Meteoritics & planetary science》1997,32(2):281-292
Abstract— We measured with a secondary ion mass spectrometer Mn/Cr ratios and Cr isotopes in individual grains of Mn-bearing sulfides (i.e., sphalerites, ZnS; alabandites, MnS; and niningerites, MgS) in nine unequilibrated enstatite chondrites (UECs). The goals were to determine whether live 53Mn (half-life ～3.7 Ma) was incorporated in these objects at the time of their isotopic closure and to establish whether Mn-Cr systematics in sulfides in UECs can be used as a high-resolution chronometer to constrain formation time differences between these meteorites. Sulfide grains analysed in four of these UECs, MAC 88136 (EL3), MAC 88184 (EL3), MAC 88180 (EL3), and Indarch (EH4), have clear 53Cr excesses. These 53Cr excesses can be very large (δ53Cr/52Cr ranges up to ～18,400%, the largest 53Cr excess measured so far) and, in some grains, are well correlated with the Mn/Cr ratios. Thus, they were most likely produced by the in situ decay of 53Mn in the meteorite samples. In the remaining five meteorites, no detectable excesses of 53Cr were found, and only upper limits on the initial 53Mn/55Mn ratios could be established. The four meteorites with 53Cr excesses show variations in the inferred 53Mn/55Mn ratios in various sulfide grains of the same meteorite. The Mn-Cr systematics in these sulfides were disturbed (during and/or after the decay of 53Mn) by varying degrees of reequilibration. Provided 53Mn was homogeneously distributed in the region of the early solar system where these objects formed, the data suggest that the time of the last isotopic equilibration of sulfides in EL chondrites occurred at least 3 Ma after a similar episode in EH chondrites. 相似文献
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Abstract— Rare earth element (REE) and other selected trace and minor element concentrations were measured in individual grains of orthopyroxene, feldspathic glass (of plagioclase composition) and merrillite of the ALH 84001 Martian meteorite. Unlike in other Martian meteorites, phosphate is not the main REE carrier in ALH 84001. The REE pattern of ALH 84001 bulk rock is dependent on the modal abundances of three REE-bearing phases, namely, orthopyroxene, which contains most of the heavy rare earth elements (HREEs); feldspathic glass, which dominates the Eu abundances; and merrillite, which contains the majority of the light rare earth elements (LREEs). Variations in the REE abundances previously observed in different splits of ALH 84001 can easily be explained in terms of small variations in the modal abundances of these three minerals without the need to invoke extensive redistribution of LREEs. At least some orthopyroxenes (i.e., those away from contacts with feldspathic glass) in ALH 84001 appear to have preserved their original REE zonation from igneous fractionation. An estimate of the ALH 84001 parent magma composition from that of the unaltered orthopyroxene “core” (i.e., zoned orthopyroxene with the lowest REE abundances) indicates that it is LREE depleted. This implies that the Martian mantle was already partly depleted within ～100 Ma of solar system formation, which is consistent with rapid accretion and differentiation of Mars. Although equilibration and exchange of REEs between phases (in particular, transport of LREEs into the interstitial phases, feldspathic glass and merrillite) cannot be ruled out, our data suggest that the LREE enrichment in melts “in equilibrium” with these interstitial phases is most likely the result of late-stage infiltration of the cumulate pile by a LREE-enriched melt. 相似文献
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Abstract— Polymict ureilites contain various mineral and lithic clasts not observed in monomict ureilites, including plagioclase, enstatite, feldspathic melt clasts and dark inclusions. This paper investigates the microdistributions and petrogenetic implications of rare earth elements (REEs) in three polymict ureilites (Elephant Moraine (EET) 83309, EET 87720 and North Haig), focusing particularly on the mineral and lithic clasts not found in monomict ureilites. As in monomict ureilites, olivine and pyroxene are the major heavy (H)REE carriers in polymict ureilites. They have light (L)REE‐depleted patterns with little variation in REE abundances, despite large differences in major element compositions. The textural and REE characteristics of feldspathic melt clasts in the three polymict ureilites indicate that they are most likely shocked melt that sampled the basaltic components associated with ureilites on their parent body. Simple REE modeling shows that the most common melt clasts in polymict ureilites can be produced by 20–30% partial melting of chondritic material, leaving behind a ureilitic residue. The plagioclase clasts, as well as some of the high‐Ca pyroxene grains, probably represent plagioclase‐pyroxene rock types on the ureilite parent body. However, the variety of REE patterns in both plagioclase and melt clasts cannot be the result of a single igneous differentiation event. Multiple processes, probably including shock melting and different sources, are required to account for all the REE characteristics observed in lithic and mineral clasts. The C‐rich matrix in polymict ureilites is LREE‐enriched, like that in monomict ureilites. The occurrence of Ce anomalies in C‐rich matrix, dark inclusions and the presence of the hydration product, iddingsite, imply significant terrestrial weathering. A search for 26Mg excesses, from the radioactive decay of 26Al, in the polymict ureilite EET 83309 was negative. 相似文献
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