Hydrogen isotopic composition of the Martian mantle inferred from the newest Martian meteorite fall,Tissint

The hydrogen isotopic composition of planetary reservoirs can provide key constraints on the origin and history of water on planets. The sources of water and the hydrological evolution of Mars may be inferred from the hydrogen isotopic compositions of mineral phases in Martian meteorites, which are currently the only samples of Mars available for Earth‐based laboratory investigations. Previous studies have shown that δD values in minerals in the Martian meteorites span a large range of ?250 to +6000‰. The highest hydrogen isotope ratios likely represent a Martian atmospheric component: either interaction with a reservoir in equilibrium with the Martian atmosphere (such as crustal water), or direct incorporation of the Martian atmosphere due to shock processes. The lowest δD values may represent those of the Martian mantle, but it has also been suggested that these values may represent terrestrial contamination in Martian meteorites. Here we report the hydrogen isotopic compositions and water contents of a variety of phases (merrillites, maskelynites, olivines, and an olivine‐hosted melt inclusion) in Tissint, the latest Martian meteorite fall that was minimally exposed to the terrestrial environment. We compared traditional sample preparation techniques with anhydrous sample preparation methods, to evaluate their effects on hydrogen isotopes, and find that for severely shocked meteorites like Tissint, the traditional sample preparation techniques increase water content and alter the D/H ratios toward more terrestrial‐like values. In the anhydrously prepared Tissint sample, we see a large range of δD values, most likely resulting from a combination of processes including magmatic degassing, secondary alteration by crustal fluids, shock‐related fractionation, and implantation of Martian atmosphere. Based on these data, our best estimate of the δD value for the Martian depleted mantle is ?116 ± 94‰, which is the lowest value measured in a phase in the anhydrously prepared section of Tissint. This value is similar to that of the terrestrial upper mantle, suggesting that water on Mars and Earth was derived from similar sources. The water contents of phases in Tissint are highly variable, and have been affected by secondary processes. Considering the H₂O abundances reported here in the driest phases (most likely representing primary igneous compositions) and appropriate partition coefficients, we estimate the H₂O content of the Tissint parent magma to be ≤0.2 wt%.     

Petrology,geochemistry, and cosmic‐ray exposure age of Iherzolitic shergottite Northwest Africa 1950

Northwest Africa (NWA) 1950 is a new member of the lherzolitic shergottite clan of the Martian meteorites recently found in the Atlas Mountains. The petrological, mineralogical, and geochemical data are very close to those of the other known lherzolitic shergottites. The meteorite has a cumulate gabbroic texture and its mineralogy consists of olivine (Fo₆₆ to Fo₇₅), low and high‐Ca pyroxenes (En₇₈Fs₁₉Wo₂‐En₆₀Fs₂₆W₁₄; En₅₃Fs₁₆Wo₃₁‐En₄₅Fs₁₄Wo₄₁), and plagioclase (An₅₇Ab₄₁Or₁ to An₄₀Ab₅₇Or₃; entirely converted into maskelynite during intense shock metamorphism). Accessory minerals include phosphates (merrillite), chromite and spinels, sulfides, and a glass rich in potassium. The oxygen isotopic values lie on the fractional line defined by the other SNC meteorites (Δ¹⁷O = 0.312 %o). The composition of NWA 1950 is very similar to the other lherzolitic shergottites and suggests an origin from the same magmatic system, or at least crystallization from a close parental melt. Cosmogenic ages indicate an ejection age similar to those of the other lherzolitic shergottites. The intensity of the shock is similar to that observed in other shergottites, as shown by the occurrence of small melt pockets containing glass interwoven with stishovite.     

Minor element zoning and trace element geochemistry of pallasites

Abstract— I report here on an ion probe study of minor element spatial distributions and trace element concentrations in six pallasites. Pallasite olivines exhibit ubiquitous minor element zoning that is independent of grain size, morphology, and adjacent phases. Ca, Cr, Ti, V, and Ni concentrations decrease from center to rim by factors of up to 10, while Mn is generally unzoned or increases slightly at the very edge of some olivine grains. The maximum concentrations of these elements at the center of olivine vary from grain to grain within the same meteorite and among the pallasites studied. These zoning profiles are consistent with thermal diffusion during rapid cooling. The inferred cooling rates at high temperature regimes are orders of magnitude faster than the low‐temperature metallographic cooling rates (?0.5 to 2°C/Ma). This suggests that pallasites, like mesosiderites, have experienced rather complicated thermal histories, i.e., cooling rapidly at high temperatures and slowly at low temperatures. Pallasite olivines are essentially free of REEs. However, the phosphates display a wide range of REE abundances (0.001 to 100 x CI) with distinct patterns. REEs are generally homogeneous within a given grain but vary significantly from grain to grain by a factor of up to 100. Albin and Imilac whitlockite are highly enriched in HREEs (?50 x CI) but are relatively depleted in LREEs (?0.1 to 1 x CI). Eagle Station whitlockite has a very unusual REE pattern: flat LREEs at a 0.1 x CI level, a large positive Eu anomaly, and a sharp increase from Gd (0.1 x CI) to Lu (70 x CI). Eagle Station stanfieldite has a similar REE pattern to that of whitlockite but with much lower REEs by a factor of 10 to 100. Springwater farringtonite has relatively low REE concentrations (0.001 to 1 x CI) with a highly fractionated HREE‐enriched pattern (CI‐normalized Lu/La ?100). Postulating any igneous processes that could have fractionated REEs in these phosphates is difficult. Possibly, phosphates were incorporated into pallasites during mixing of olivine and IIIAB‐like molten Fe. These phosphates preserve characteristics of a previous history. Pallasites have not necessarily formed at the mantle‐core boundary of their parent bodies. The pallasite thermal histories suggest that pallasites may have formed at a shallow depth and were subsequently buried deep under a regolith blanket.     

The lherzolitic shergottite Grove Mountains 99027: Rare earth element geochemistry

Abstract— We report here on an ion probe study of rare earth element (REE) geochemistry in the lherzolitic shergottite Grove Mountains (GRV) 99027. This meteorite shows almost identical mineralogy, petrology, and REE geochemistry to those of the lherzolitic shergottites Allan Hills (ALH) A77005, Lewis Cliff (LEW) 88516, and Yamato (Y‐) 793605. REE concentrations in olivine, pyroxenes, maskelynite, merrillite, and melt glass are basically comparable to previous data obtained from ALH A77005, LEW 88516, and Y‐793605. Olivine is the dominant phase in this meteorite. It is commonly enclosed by large (up to several mm) pigeonite oikocrysts. Non‐poikilitic areas consist of larger olivine grains (?mm), pigeonite, augite, and maskelynite. Minor merrillite (up to 150 μm in size) is widespread in non‐poikilitic regions, occurring interstitially between olivine and pyroxene grains. It is the main REE carrier in GRV 99027 and has relatively higher REEs (200–1000 × CI) than that of other lherzolitic shergottites. A REE budget calculation for GRV 99027 yields a whole rock REE pattern very similar to that of other lherzolites. It is characterized by the distinctive light REE depletion and a smooth increase from light REEs to heavy REEs. REE microdistributions in GRV 99027 strongly support the idea that all lherzolitic shergottites formed by identical igneous processes, probably from the same magma chamber on Mars. Despite many similarities in mineralogy, petrography, and trace element geochemistry, subtle differences exist between GRV 99027 and other lherzolitic shergottites. GRV 99027 has relatively uniform mineral compositions (both major elements and REEs), implying that it suffered a higher degree of sub‐solidus equilibration than the other three lherzolites. It is notable that GRV 99027 has experienced terrestrial weathering in the Antarctic environment, as its olivine and pyroxenes commonly display a light REE enrichment and a negative Ce anomaly. Caution needs to be taken in future chronological studies.     

Chondrule trace element geochemistry at the mineral scale

Abstract– We report trace element analyses from mineral phases in chondrules from carbonaceous chondrites (Vigarano, Renazzo, and Acfer 187), carried out by laser ablation inductively coupled plasma‐mass spectrometry. Results are similar in all three meteorites. Mesostasis has rare earth element (REE) concentrations of 10–20 × CI. Low‐Ca pyroxene has light REE (LREE) concentrations near 0.1 × CI and heavy REE (HREE) near 1 × CI, respectively. Olivine has HREE concentrations at 0.1–1 × CI and LREE around 10^?2 × CI. The coarsest olivine crystals tend to have the most fractionated REE patterns, indicative of equilibrium partitioning. Low‐Ca pyroxene in the most pyroxene‐rich chondrules tends to have the lowest REE concentrations. Type I chondrules seem to have undergone a significant degree of batch crystallization (as opposed to fractional crystallization), which requires cooling rates slower than 1–100 K h^?1. This would fill the gap between igneous calcium‐aluminum‐rich inclusions (CAIs) and type II chondrules. The anticorrelation between REE abundances and pyroxene mode may be understood as due to dilution by addition of silica to the chondrule melt, as in the gas‐melt interaction scenario of Libourel et al. (2006). The rapid cooling rate (of the order of 1000 K h^?1) which seems recorded by low‐Ca pyroxene, contrasted with the more diverse record of olivine, may point to a nonlinear cooling history or suggest that formation of pyroxene‐rich chondrule margins was an event distinct from the crystallization of the interior.     

Petrography,mineralogy, and trace element geochemistry of lunar meteorite Dhofar 1180

Abstract— Here we report the petrography, mineralogy, and trace element geochemistry of the Dhofar 1180 lunar meteorite. Dhofar 1180 is predominantly composed of fine‐grained matrix with abundant mineral fragments and a few lithic and glassy clasts. Lithic clasts show a variety of textures including cataclastic, gabbroic, granulitic, ophitic/subophitic, and microporphyritic. Both feldspathic and mafic lithic clasts are present. Most feldspathic lithic clasts have a strong affinity to ferroan anorthositic suite rocks and one to magnesian suite rocks. Mafic lithic clasts are moderately to extremely Fe‐rich. The Ti/[Ti+Cr]‐Fe/[Fe+Mg] compositional trend of pyroxenes in mafic lithic clasts is consistent with that of low‐Ti mare basalts. Glasses display a wide chemical variation from mafic to feldspathic. Some glasses are very similar to those from Apollo 16 soils. KREEP components are essentially absent in Dhofar 1180. One glassy clast is rich in K, REE and P, but its Mg/[Mg+Fe] is very low (0.25). It is probably a last‐stage differentiation product of mare basalt. Molar Fe/Mn ratios of both olivine and pyroxene are essentially consistent with a lunar origin. Dhofar 1180 has a LREE‐enriched (La 18 × CI, Sm 14 × CI) pattern with a small positive Eu anomaly (Eu 15 × CI). Th concentration is 0.7 ppm in Dhofar 1180. Petrography, mineralogy, and trace element geochemistry of Dhofar 1180 are different from those of other lunar meteorites, indicating that Dhofar 1180 represents a unique mingled lunar breccia derived from an area on the lunar nearside but far away from the center of the Imbrium Basin.     

Petrology and chemistry of the basaltic shergottite North West Africa 480

Abstract— North West Africa (NWA) 480 is a new martian meteorite of 28 g found in the Moroccan Sahara in November 2000. It consists mainly of large gray pyroxene crystals (the largest grains are up to 5 mm in length) and plagioclase converted to maskelynite. Excluding the melt pocket areas, modal analyses indicate the following mineral proportions: 72 vol% pyroxenes extensively zoned, 25% maskelynite, 1% phosphates (merrillite and chlorapatite), 1% opaque oxides (ilmenite, ulvöspinel and chromite) and sulfides, and 1% others such as silica and fayalite. The compositional trend of NWA 480 pyroxenes is similar to that of Queen Alexandra Range (QUE) 94201 but in NWA 480 the pyroxene cores are more Mg‐rich (En₇₇‐En₆₅). Maskelynites display a limited zoning (An_42–50Ab_54‐48Or_2–4). Our observations suggest that NWA 480 formed from a melt with a low nuclei density at a slow cooling rate. The texture was achieved via a single‐stage cooling where pyroxenes grew continuously. A similar model was previously proposed for QUE 94201 by McSween et al. (1996). NWA 480 is an Al‐poor ferroan basaltic rock and resembles Zagami or Shergotty for major elements and compatible trace element abundances. The bulk rock analysis for oxygen isotopes yields Δ¹⁷O = +0.42%, a value in agreement at the high margin, with those measured on other shergottites (Clayton and Mayeda, 1996; Romanek et al., 1998; Franchi et al., 1999). Its CI‐normalized rare earth element pattern is similar to those of peridotitic shergottites such as Allan Hills (ALH)A77005, suggesting that these shergottites shared a similar parent liquid, or at least the same mantle source.     

Petrology and chemistry of the new shergottite Dar al Gani 476

Abstract— In 1998, Dar al Gani (DaG) 476 was found in the Libyan desert. The meteorite is classified as a basaltic shergottite and is only the 13th martian meteorite known to date. It has a porphyritic texture consisting of a fine‐grained groundmass and larger olivines. The groundmass consists of pyroxene and feldspathic glass. Minor phases are oxides and sulfides as well as phosphates. The presence of olivine, orthopyroxene, and chromite is a feature that DaG 476 has in common with lithology A of Elephant Moraine (EET) A79001. However, in DaG 476, these phases appear to be early phenocrysts rather than xenocrysts. Shock features, such as twinning, mosaicism, and impact‐melt pockets, are ubiquitous. Terrestrial weathering was severe and led to formation of carbonate veins following grain boundaries and cracks. With a molar MgO/(MgO + FeO) of 0.68, DaG 476 is the most magnesian member among the basaltic shergottites. Compositions of augite and pigeonite and some of the bulk element concentrations are intermediate between those of lherzolitic and basaltic shergottites. However, major elements, such as Fe and Ti, as well as LREE concentrations are considerably lower than in other shergottites. Noble gas concentrations are low and dominated by the mantle component previously found in Chassigny. A component, similar to that representing martian atmosphere, is virtually absent. The ejection age of 1.35 ± 0.10 Ma is older than that of EETA79001 and could possibly mark a distinct ejection. Dar al Gani 476 is classified as a basaltic shergottite based on its mineralogy. It has a fine‐grained groundmass consisting of clinopyroxene, pigeonite and augite, feldspathic glass and chromite, Ti‐chromite, ilmenite, sulfides, and whitlockite. Isolated olivine and single chromite grains occur in the groundmass. Orthopyroxene forms cores of some pigeonite grains. Shock‐features, such as shock‐twinning, mosaicism, cracks, and impact‐melt pockets, are abundant. Severe weathering in the Sahara led to significant formation of carbonate veins crosscutting the entire meteorite. Dar al Gani 476 is distinct from other known shergottites. Chemically, it is the most magnesian member among known basaltic shergottites and intermediate in composition for most trace and major elements between Iherzolitic and basaltic shergottites. Unique are the very low bulk REE element abundances. The CI‐normalized abundances of LREEs are even lower than those of Iherzolitic shergottites. The overall abundance pattern, however, is similar to that of QUE 94201. Textural evidence indicates that orthopyroxene, as well as olivine and chromite, crystallized as phenocrysts from a magma similar in composition to that of bulk DaG 476. Whether such a magma composition can be a shergottite parent melt or was formed by impact melting needs to be explored further. At this time, it cannot entirely be ruled out that these phases represent relics of disaggregated xenoliths that were incorporated and partially assimilated by a basaltic melt, although the texture does not support this possibility. Trapped noble gas concentrations are low and dominated by a Chassigny‐like mantle component. Virtually no martian atmosphere was trapped in DaG 476 whole‐rock splits. The exposure age of 1.26 ± 0.09 Ma is younger than that of most shergottites and closer to that of EETA79001. The ejection age of 1.35 ± 0.1 Ma could mark another distinct impact event.     

Petrology and geochemistry of D'Orbigny,geochemistry of Sahara 99555, and the origin of angrites

Abstract— We have done a detailed petrologic study of the angrite, D'Orbigny, and geochemical study of it and Sahara 99555. D'Orbigny is an igneous‐textured rock composed of Ca‐rich olivine, Al‐Ti‐diopside‐hedenbergite, subcalcic kirschsteinite, two generations of hercynitic spinel and anorthite, with the mesostasis phases ulvöspinel, Ca‐phosphate, a silico‐phosphate phase and Fe‐sulfide. We report an unknown Fe‐Ca‐Al‐Ti‐silicate phase in the mesostasis not previously found in angrites. One hercynitic spinel is a large, rounded homogeneous grain of a different composition than the euhedral and zoned grains. We believe the former is a xenocryst, the first such described from angrites. The mafic phases are highly zoned; mg# of cores for olivine are ?64, and for clinopyroxene ?58, and both are zoned to Mg‐free rims. The Ca content of olivine increases with decreasing mg#, until olivine with ?20 mol% Ca is overgrown by subcalcic kirschsteinite with about 30–35 mol% Ca. Detailed zoning sequences in olivine‐subcalcic kirschsteinite and clinopyroxene show slight compositional reversals. There is no mineralogic control that can explain these reversals, and we believe they were likely caused by local additions of more primitive melt during crystallization of D'Orbigny. D'Orbigny is the most ferroan angrite with a bulk rock mg# of 32. Compositionally, it is virtually identical to Sahara 99555; they are the first set of compositionally identical angrites. Comparison with the other angrites shows that there is no simple petrogenetic sequence, partial melting with or without fractional crystallization, that can explain the angrite suite. Angra dos Reis remains an anomalous angrite. Angrites show no evidence for the brecciation, shock, impact metamorphism, or thermal metamorphism that affected the howardite, eucrite, diogenite (HED) suite and ordinary chondrites. This suggests that the angrite parent body may have followed a fundamentally different evolutionary path than did these other parent bodies.     

The basaltic shergottite Northwest Africa 856: Petrology and chemistry

Abstract— We report on the discovery of a new shergottite from South Morocco. This single stone weighing 320 g is referenced as Northwest Africa (NWA) 856 with Djel Ibone as a synonymous name. It is a fresh, fine‐grained basaltic rock consisting mainly of two pyroxenes (total ?68 vol%: 45% pigeonite, En_61‐16Wo_9–22Fs_26–68; 23% augite, En_46‐26Wo_34‐29Fs_21–43) and plagioclase converted to maskelynite (?23 vol%, Ab_43–57Or_1–5An_54‐36). Accessory minerals include merrillite, Cl‐apatite, pyrrhotite, ilmenite, ulvöspinel, silica (stishovite and glass), amorphous K‐feldspar and baddeleyite. Amorphous mixtures of maskelynite and silica occur most commonly as median layers inside maskelynite laths. In addition, melt pockets (?2 vol%) were recognized with relics of maskelynite, pyroxene and both dense silica glass and stishovite occurring as both grains and submicrometer needles. The compositions of the melt pockets are consistent with mixtures of maskelynite and pyroxenes with an average of ?50 vol% maskelynite. The meteorite is highly fractured at all scales. The bulk composition of NWA 856 has been measured for 44 elements. It is an Al‐poor ferroan basaltic rock which strongly resembles Shergotty and Zagami in its major and trace element composition. The nearly flat rare earth element (REE) pattern (La/Lu)_n = 0.9, is similar to that of Shergotty or Zagami and differs significantly from NWA 480, another Moroccan shergottite recently described. According to the U, Ba and Sr abundances, NWA 856 is not significantly weathered. The oxygen isotopes (δ18O = +5.03%, δ17O = +3.09%, and Δ17O = +0.47%) are in agreement with the martian origin of this meteorite. On the basis of grain size, pyroxene zoning and composition, abundance of silica inclusions associated with maskelynite, trace element abundances, REE pattern and oxygen isotopes, pairing with NWA 480 is excluded. The similarity with Shergotty and Zagami is striking. The only significant differences are a larger grain size, a greater abundance of silica and melt pockets, a slightly more restricted range of pyroxene compositions and the absence of significant mesostasis.     

Petrology and shock history of the first depleted-like poikilitic shergottite Asuka 12325

Asuka (A) 12325 is the first poikilitic shergottite having a depleted pattern in light rare earth elements (REE). Compared with known poikilitic shergottites, A 12325 has smaller but more abundant pyroxene oikocrysts with remarkable Fe-rich pigeonite rims, indicating that A 12325 cooled relatively faster at a shallower part of the crust. The redox condition (logfO₂ = IW + 0.6-IW + 1.7) and Fe-rich chemical compositions of each mineral in A 12325 are close to enriched shergottites. The intermediate shergottites could not form by a simple mixing between parent magmas of A 12325 and enriched shergottites. Although A 12325 contains various high-pressure minerals such as majorite and ringwoodite, plagioclase is only partly maskelynitized. Therefore, the maximum shock pressure may be within 17–22 GPa. Thermal conduction and ringwoodite growth calculation around a shock vein revealed that the shock dwell time of A 12325 is at least 40 ms. The weaker shock pressure and longer shock dwell time in A 12325 may be attained by an impact event similar to those of nakhlites and Northwest Africa (NWA) 8159. Such a weak shock ejection event may be as common on Mars as a severe shock event recorded in shergottites. Alteration of sulfide observed in A 12325 may imply the presence of magmatic fluid in its reservoir on Mars. A 12325 expands a chemical variety of Martian rocks and has a unique shock history among poikilitic shergottites while A 12325 also implies that poikilitic shergottites are common rocks on Mars regardless of their sources.     

Petrography and geochemistry of the enriched basaltic shergottite Northwest Africa 2975

We present a study of the petrology and geochemistry of basaltic shergottite Northwest Africa 2975 (NWA 2975). NWA 2975 is a medium‐grained basalt with subophitic to granular texture. Electron microprobe (EMP) analyses show two distinct pyroxene compositional trends and patchy compositional zoning patterns distinct from those observed in other meteorites such as Shergotty or QUE 94201. As no bulk sample was available to us for whole rock measurements, we characterized the fusion crust and its variability by secondary ion mass spectrometer (SIMS) measurements and laser ablation inductively coupled plasma spectroscopy (LA‐ICP‐MS) analyses as a best‐available proxy for the bulk rock composition. The fusion crust major element composition is comparable to the bulk composition of other enriched basaltic shergottites, placing NWA 2975 within that sample group. The CI‐normalized REE (rare earth element) patterns are flat and also parallel to those of other enriched basaltic shergottites. Merrillite is the major REE carrier and has a flat REE pattern with slight depletion of Eu, parallel to REE patterns of merrillites from other basaltic shergottites. The oxidation state of NWA 2975 calculated from Fe‐Ti oxide pairs is NNO‐1.86, close to the QFM buffer. NWA 2975 represents a sample from the oxidized and enriched shergottite group, and our measurements and constraints on its origin are consistent with the hypothesis of two distinct Martian mantle reservoirs: a reduced, LREE‐depleted reservoir and an oxidized, LREE‐enriched reservoir. Stishovite, possibly seifertite, and dense SiO₂ glass were also identified in the meteorite, allowing us to infer that NWA 2975 experienced a realistic shock pressure of ~30 GPa.     

Petrology of magmatic silicate inclusions in the Allan Hills 77005 lherzolitic shergottite

Abstract— Magmatic inclusions occur in both chadacrystic olivine and oikocrystic pigeonite in ALH 77005 but are different from each other. Magmatic inclusions in olivine consist mainly of aluminous pyroxenes, intergrowths of plagioclase and silica, silica-predominant glass, and rhyodacitic glass, with minor amounts of chromite, spinel, pyrrhotite, and whitlockite. Those in pigeonite consist mainly of aluminous pyroxenes, nonaluminous ferroan pyroxenes, kaersutite, spinel, and K-rich trachytic glass, with minor amounts of pyrrhotite and whitlockite. The magmatic inclusions in chadacrystic olivine formed from trapped melts that were basaltic, apparently dry and crystallized additional olivine metastably. The basaltic magma, with entrained olivine, experienced magma mixing with K-rich and wet magmas, or assimilation of such crustal rocks, in the early to middle stages of the crystallization sequence of ALH 77005 during crystallization of chadacrystic olivine prior to precipitation of oikocrystic pigeonite. However the amount of mixed magmas or assimilated rocks was minor in comparison to the basaltic magma. Crystallization of pigeonite, augite, and plagioclase in the host lithologies took place in a shallow magma reservoir under an open-system condition, and the pigeonite trapped basaltic andesite to trachyandesitic melts, which resulted in magmatic inclusions in oikocrystic pigeonite. The magmatic inclusions in both olivine and pigeonite were formed under a rapid-cooling condition, resulting in a variety of inclusions. Kaersutite in magmatic inclusions in oikocrystic pigeonite crystallized under a closed-system wet condition during the late-stage crystallization of the inclusions.     

Petrology and geochemistry of the Northwest Africa 3368 eucrite

Abstract– Analysis of the mineralogy, isotopic, and bulk compositions of the eucrite meteorites is imperative for understanding their origin on the asteroid 4 Vesta, the proposed parent body of the HED meteorites. We present here the petrology, mineral compositions, and bulk chemistry of several lithic components of the new brecciated basaltic eucrite Northwest Africa (NWA) 3368 to determine if all the lithologies reflect formation from one rock type or many rock types. The meteorite has three main lithologies: coarse‐ and fine‐grained clasts surrounded by a fine‐grained recrystallized silicate matrix. Silicate compositions are homogeneous, and the average rare earth element pattern for NWA 3368 is approximately 10× CI chondrites with a slight negative Eu anomaly. Major and trace element data place NWA 3368 with the Main Group‐Nuevo Laredo trend. High‐Ti chromites with ilmenite exsolution lamellae provide evidence of NWA 3368’s history of intense metamorphism. We suggest that this meteorite underwent several episodes of brecciation and metamorphism, similar to that proposed by Metzler et al. (1995) . We conclude that NWA 3368 is a monomict basaltic eucrite breccia related to known eucrites in texture and in mineral, bulk, and oxygen isotopic composition.     

Major and trace element geochemistry of S‐type cosmic spherules

Micrometeorites that pass through the Earth's atmosphere undergo changes in their chemical compositions, thereby making it difficult to understand if they are sourced from the matrix, chondrules, or calcium–aluminum‐rich inclusions (CAIs). These components have the potential to provide evidence toward the understanding of the early solar nebular evolution. The variations in the major element and trace element compositions of 155 different type (scoriaceous, relict bearing, porphyritic, barred, cryptocrystalline, and glass) of S‐type cosmic spherules are investigated with the intent to decipher the parent sources using electron microprobe and laser ablation inductively coupled plasma‐mass spectrometry. The S‐type cosmic spherules appear to show a systematic depletion in volatile element contents, but have preserved their refractory trace elements. The trends in their chemical compositions suggest that the S‐type spherules comprise of components from similar parent bodies, that is, carbonaceous chondrites. Large fosteritic relict grains observed in this investigation appear to be related to the fragments of chondrules from carbonaceous chondrites. Furthermore, four spherules (two of these spherules enclose spinels and one comprised entirely of a Ca‐Al‐rich plagioclase) show enhanced trace element enrichment patterns that are drastically different from all the other 151 cosmic spherules. The information on the chemical composition and rare earth elements (REEs) on cosmic spherules suggest that the partially to fully melted ones can preserve evidences related to their parent bodies. The Ce, Eu, and Tm anomalies found in the cosmic spherules have similar behavior as that of chondrites. Distinct correlations observed between different REEs and types of cosmic spherules reflect the inherited properties of the precursors.     

Insights into the Martian mantle: The age and isotopics of the meteorite fall Tissint

The recent witnessed fall of the meteorite Tissint represents the delivery of a pristine new sample from the surface of Mars. This meteorite provides an unprecedented opportunity to study a variety of aspects about the planet's evolution. Using the Rb–Sr and Sm–Nd isotopic systems, we determined that Tissint, a depleted shergottite, has a crystallization age of 574 ± 20 Ma, an initial ε¹⁴³Nd = +42.2 ± 0.5, and an initial ⁸⁷Sr/⁸⁶Sr = 0.700760 ± 11. These initial Nd and Sr isotopic compositions suggest that Tissint originated from a mantle source on Mars that is distinct from the source reservoirs of the other Martian meteorites. The known crystallization ages, geochemical characteristics, ejection ages, and ejection dynamics of Tissint and other similarly grouped Martian meteorites suggest that they are likely derived from a source crater up to approximately 90 km in diameter with an age of approximately 1 Ma that is located on terrain that is approximately 600 million years old.     

Small melt inclusions can record bulk magma compositions: A planetary example from the Martian basalt (shergottite) Tissint

Melt inclusions in igneous minerals can provide constraints on magma compositions, especially for planetary samples where mass is severely limited. Small inclusions (<15 μm diameter) are more abundant than large ones, but have been used little from concern that they did not entrap average magma, but are rich in melt of a diffusional layer against the host mineral. We compared bulk compositions and calculated original compositions of small and large melt inclusions in the Martian basalt meteorite (shergottite) Tissint. Small and large melt inclusions are consistent with the same line of igneous differentiation, have the same abundance ratios for incompatible elements (P, Ti, Al, K, Na), and are consistent with derivation from the bulk composition of Tissint (inferred to represent its parent melt composition). For Tissint, then, small melt inclusions show no evidence of entrapping diffusional boundary layers, and appear to have entrapped bulk magma. Thus, its small inclusions can be as useful as larger ones; this may be so for other planetary samples, and thus provides an additional tool for investigating planetary magmas.     

Petrology and geochemistry of the fine‐grained,unbrecciated diogenite Northwest Africa 4215

Abstract— We report on the petrology and geochemistry of Northwest Africa (NWA) 4215, an unbrecciated diogenite recovered in the Sahara. This single stone, weighing 46.4 g, displays a wellpreserved cumulative texture. It consists of zoned xenomorphic orthopyroxene grains on the order of 500 μm in size, along with a few large chromite crystals (<5 vol%, up to 3 mm). Accessory olivine and scarce diopside grains occur within the groundmass, usually around the chromite crystals. Minor phases are cristobalite, troilite, and metal. Unlike other diogenites, orthopyroxenes (En_76.2Wo_1.1Fs_22.7 to En_68.6Wo_5.5Fs_25.9), olivines (Fo₇₆ to Fo₇₁), and chromites (Mg# = 14.3 44.0, Cr# = 42.2–86.5) are chemically zoned. The minor element behavior in orthopyroxenes and the intricate chemical profiles obtained in chromites indicate that the zonings do not mirror the evolution of the parental melt. We suggest that they resulted from reaction of the crystals with intercumulus melt. In order to preserve the observed zoning profiles, NWA 4215 clearly cooled significantly faster than other diogenites. Indeed, the cooling rate determined from the diffusion of Cr in olivine abutting chromite is in the order of 10–50 °C/a, suggesting that NWA 4215 formed within a small, shallow intrusion. The bulk composition of NWA 4215 has been determined for major and trace elements. This meteorite is weathered and its fractures are filled with calcite, limonite, and gypsum, typical of hot desert alteration. In particular, the FeO, CaO abundances and most of the trace element concentrations (Sr, Ba, Pb, and REE among others) are high and indicate a significant contribution from the secondary minerals. To remove the terrestrial contribution, we have leached with HCl a subsample of the meteorite. The residue, made essentially of orthopyroxene and chromite, has similar major and trace element abundances to diogenites as shown by the shape of its REE pattern or by its high Al/Ga ratio. The connection of NWA 4215 with diogenites is confirmed by its O‐isotopic composition (δ¹⁷O = 1.431 ± 0.102‰, δ¹⁸O = 3.203 ± 0.205‰, Δ¹⁷O = ?0.248 ± 0.005‰).     

Thuathe,a new H4/5 chondrite from Lesotho: History of the fall,petrography, and geochemistry

Abstract— On July 21, 2002, a meteorite fall occurred over the Thuathe plateau of western Lesotho. The well‐defined strewn field covers an area of 1.9 times 7.4 km. Many of the recovered specimens display a brecciated texture with leucocratic, angular to subrounded clasts in a somewhat darker groundmass. Mineralogical and chemical data, as well as oxygen isotopic analysis, indicate that Thuathe is an H4/5, S2/3 meteorite, with local H3 or H6 character. A number of anomalous features include somewhat high Co contents of kamacite and taenite relative to normal H‐group chondrites. Oxygen isotopic data plot at the edge of the normal H chondrite data field. Variable contents of metallic mineral phases and troilite result in a heterogeneous bulk composition (e.g., with regard to Si, Fe, and Mg), resulting in a spread of major element ratios that is not consistent with previously accepted H‐group composition. Trace element abundances are generally consistent with H chondritic composition, and Kr and Xe isotopic data agree with an H4 classification for this meteorite. Noble gas analysis gave U, Th‐⁴He gas retention and K‐Ar ages typical for H chondrites; no major thermal event affected this material since ～3.7 Ga. The exposure age for Thuathe is 5 Ma, somewhat lower than for other H chondrites. Cosmogenic nuclide analysis indicates a pre‐atmospheric radius of this meteorite between 35 and 40 cm. In the absence of evidence for solar gases, we classify Thuathe as a fragmental breccia. Numerous narrow, black veins cut across samples of Thuathe and are the result of a brittle deformation event that also caused local melting, especially in portions rich in sulfide. The formation of these veinlets is not the result of locally enhanced shock pressures (i.e., of shock melting) but rather of shearing under brittle conditions with local, friction‐related temperature excursions causing melting mostly of Fe‐sulfide and FeNi‐metal but also, locally, of silicate minerals. Frictional temperature excursions must have attained values in excess of 1500 °C to permit complete melting of forsteritic olivine.