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‰).     

Petrology and geochemistry of Northwest Africa 5480 diogenite and evidence for a basin‐forming event on Vesta

We performed a petrological and geochemical study of an olivine diogenite, Northwest Africa (NWA) 5480. NWA 5480 is a crystalline stone, but shows a heterogeneous texture. Olivine aggregates and grains of olivine and chromite display resorption textures set in a crystalline pyroxene matrix. Large olivine aggregates are penetrated by pyroxene matrix. Flow textures are observed near olivine aggregates. Olivine, chromite, and pyroxene show minor chemical zoning, implying relatively rapid cooling. NWA 5480 contains a significant amount of platinum group elements with chondritic relative proportions. All this evidence supports that NWA 5480 is an impact‐melt breccia from a target composed of olivine and pyroxene‐rich lithologies. Such impact melt would have formed by melting crustal materials, possibly during one of the impacts that formed the South Pole basins on Vesta.     

An impact-melt origin for lithology A of martian meteorite Elephant Moraine A79001

Abstract— Mixing models using major and trace elements show that the bulk composition of lithology A (xenocryst-bearing magnesian basalt) of Elephant Moraine A79001 (EETA79001) can be reasonably approximated as a simple mixture of ～44% EETA79001 lithology B (ferroan basalt) and ～56% of Allan Hills A77005 (ALHA7705) light lithology (incompatible element-poor lherzolite). Micro-instrumental neutron activation analysis (INAA) data on xenocryst-free groundmass samples of lithology A show that about 20–25% of the melt phase could be dissolved lherzolite. The bulk and groundmass samples of lithology A have excesses in Au, which indicates either meteoritic contamination or addition by some unknown martian geochemical process. Previous workers have suggested that lithology A was formed by either assimilation of cumulates (like ALHA77005), by a basalt (like lithology B), or by mixing of basaltic and lherzolitic magmas. The former scenario is energetically improbable and unlikely to explain the normal Fe/Mg zonation in lithology A groundmass pyroxenes, whereas the latter scenario is unlikely to satisfy the constraints of the mixing model indicating the ultramafic component is poor in incompatible elements. We suggest rather that EETA79001 lithology A is an impact melt composed dominantly of basalt like lithology B and lherzolitic cumulates like the trace-element-poor fraction of ALHA77005 or Y-793605. This model can satisfy the energetic, petrologic, and geochemical constraints imposed by the samples. If EETA79001 lithology A is an impact melt, this would have considerable consequences for current models of martian petrologic evolution. It would call into question the generally accepted age of magmatism of martian basalts and preclude the use of lithology A groundmass as a primary martian basalt composition in experimental studies. Regardless, the latter is required because lithology A groundmass is a hybrid composition.     

Portales Valley: Petrology of a metallic‐melt meteorite breccia

Abstract— Portales Valley (PV) is an unusual metal‐veined meteorite that has been classified as an H6 chondrite. It has been regarded either as an annealed impact melt breccia, as a primitive achondrite, or as a meteorite with affinities to silicated iron meteorites. We studied the petrology of PV using a variety of geochemical‐mineralogical techniques. Our results suggest that PV is the first well‐documented metallic‐melt meteorite breccia. Mineral‐chemical and other data suggest that the protolith to PV was an H chondrite. The composition of FeNi metal in PV is somewhat fractionated compared to H chondrites and varies between coarse vein and silicate‐rich portions. It is best modeled as having formed by partial melting at temperatures of ?940–1150 °C, with incomplete separation of solid from liquid metal. Solid metal concentrated in the coarse vein areas and S‐bearing liquid metal concentrated in the silicate‐rich areas, possibly as a result of a surface energy effect. Both carbon and phosphorus must have been scavenged from large volumes and concentrated in metallic liquid. Graphite nodules formed by crystallization from this liquid, whereas phosphate formed by reaction between P‐bearing metal and clinopyroxene components, depleting clinopyroxene throughout much of the meteorite and growing coarse phosphate at metal‐silicate interfaces. Some phosphate probably crystallized from P‐bearing liquids, but most probably formed by solid‐state reaction at ?975‐725 °C. Phosphate‐forming and FeO‐reduction reactions were widespread in PV and entailed a change in the mineralogy of the stony portion on a large scale. Portales Valley experienced protracted annealing from supersolidus to subsolidus temperatures, probably by cooling at depth within its parent body, but the main differences between PV and H chondrites arose because maximum temperatures were higher in PV. A combination of a relatively weak shock event and elevated pre‐shock temperatures probably produced the vein‐and‐breccia texture, with endogenic heating being the main heat source for melting, and with stress waves from an impact event being an essential trigger for mobilizing metal. Portales Valley is best classified as an H7 metallic‐melt breccia of shock stage S1. The meteorite is transitional between more primitive (chondritic) and evolved (achondrite, iron) meteorite types and offers clues as to how differentiation could have occurred in some asteroidal bodies.     

Multiple origins of xenoliths and xenocrysts in the Elephant Moraine 79001 Lithology A olivine‐phyric shergottite

Petrographic examination of the xenolith and xenocryst populations in the olivine‐phyric shergottite Elephant Moraine 79001 Lithology A shows more chemical heterogeneity than previously documented. Analyses of olivine grains in 18 megacrysts and in 4 lithic fragments show that these two populations either do not have the same source or that this source is heterogeneous in terms of its time–temperature history. Additionally, among the four lithic fragments analyzed, two are distinctive (1) one contains a major‐element‐equilibrated, euhedral olivine grain and (2) the second contains high‐magnesium pyroxene cores. Furthermore, two populations of ferroan olivine were identified (1) one more ferroan than any other reported in EET 79001 and (2) a slightly less ferroan, unequilibrated olivine, but with a restricted range in Mg#. We have also observed an equilibrated pyroxene grain associated with a zoned olivine megacryst. As a result, we recognize that the xenolith/xenocryst population does not represent the incorporation of a single xeno‐lithology into Lithology A, and propose that it be subdivided into a suite of seven identified lithologies, with the understanding that more are likely to be identified with further study. The abundance of Ca in olivine in the xeno‐lithologies suggests a set of crustal, rather than deep mantle, lithologies. Diffusion rates in olivine suggest that the lithologies were incorporated shortly before rapid cooling of the host magma, preserving preexisting mineral chemical zoning. These mineral chemical zones could have been preserved at lower crustal temperatures for up to 10s of Ka. Trace‐element studies of these distinct populations would be required to test whether they are related by igneous processes from a common source magma.     

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.     

An experimental and petrographic investigation of Elephant Moraine 79001 lithology A: Implications for its petrogenesis and the partitioning of chromium and vanadium in a martian basalt

Abstract— A composition approximating the lithology A groundmass of the Elephant Moraine (EET) 79001 martian basalt (Eg; McSween and Jarosewich, 1983) has been used to investigate the petrogenesis of the meteorite and the behavior of Cr and V at different oxygen fugacities. Crystallization experiments were carried out over a range of temperatures, and oxygen fugacities of either iron‐wüstite (IW) or IW + 2 (i.e., 1.5 log units below the quartz‐fayalite‐magnetite (QFM) buffer). Comparison of trace element concentrations (obtained by secondary ion mass spectrometry (SIMS) analysis) in experimental silicates with those of natural silicates supports the Fe‐Ti oxide‐derived oxygen fugacity of QFM ?1.8 ± 0.3 for this basalt (Herd et al., 2001). Experimental distribution coefficients, in conjunction with SIMS analyses of rims from the olivine and pyroxene xenocrysts in lithology A, as well as analyses of lithology A groundmass pigeonite cores, are used to calculate coexisting liquid concentrations of V and Cr. Liquid compositions derived from pigeonite xenocryst rims and groundmass pigeonite cores are similar, suggesting that the rims of orthopyroxene xenocrysts are overgrowths, which have not previously been accounted for when reconstructing the groundmass composition. This implies that the Eg composition requires modification. A similar exercise for the ferroan rims on olivine xenocrysts yields very different liquid compositions, indicating that these rims are not overgrowths but are part of the xenocryst assemblage. These results are shown to be consistent with the petrography of lithology A xenocrysts.     

Petrology and geochemistry of feldspathic impact‐melt breccia Abar al' Uj 012, the first lunar meteorite from Saudi Arabia

Abar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al₂O₃, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An_96.9Ab_3.0Or_0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm² exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO₂ than any mare basalt. It also has higher FeO and lower Al₂O₃ than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.     

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.     

Lunar surface exposure models for meteorites Elephant Moraine 96008 and Dar al Gani 262 from the Moon

Abstract— We derived the cosmic‐ray and solar particle exposure history for the two lunar meteorites Elephant Moraine (EET) 96008 and Dar al Gani (DaG) 262 on the basis of the noble gas isotopic abundances including the radionuclide ⁸¹Kr. For EET 96008, we propose a model for the exposure to cosmic rays and solar particles in three stages on the Moon: an early stage ～500 Ma ago, lasting less than 9 Ma at a shallow shielding depth of 20 g/cm², followed by a stage when the material was buried, without exposure, until it was exposed in a recent stage. This recent stage, at a shielding depth in a range of 200–600 g/cm², lasted for ～26 Ma until ejection. This model is essentially the same as that previously found for lunar meteorite EET 87521; thus, pairing of the two Elephant Moraine lunar meteorites that were recovered on the same icefield in Antarctica is confirmed by our data. The cosmic‐ray‐produced isotopes, the trapped solar and lunar atmospheric noble gases, as well as the radionuclide ⁸¹Kr observed for the DaG 262 lunar meteorite are consistent with a one‐stage lunar exposure history. The average burial depth of the Dar al Gani material before ejection was within a range of 50–80 g/cm². The exposure to cosmic rays at this depth lasted 500–1000 Ma. This long residence time for Dar al Gani at relatively shallow depth explains the high concentrations of implanted solar noble gases.     

Alteration assemblages in the Miller Range and Elephant Moraine regions of Antarctica: Comparisons between terrestrial igneous rocks and Martian meteorites

The weathering products present in igneous terrestrial Antarctic samples were analyzed, and compared with those found in the four Miller Range nakhlite Martian meteorites. The aim of these comparisons was to determine which of the alteration phases in the Miller Range nakhlites are produced by terrestrial weathering, and what effect rock composition has on these phases. Antarctic terrestrial samples MIL 05031 and EET 96400, along with the Miller Range nakhlites MIL 03346 and 090032, were found to contain secondary alteration assemblages at their externally exposed surfaces. Despite the difference in primary mineralogy, the assemblages of these rocks consist mostly of sulfates (jarosite in MIL 05031, jarosite and gypsum in EET 96400) and iddingsite‐like Fe‐clay. As neither of the terrestrial samples contains sulfur‐bearing primary minerals, and these minerals are rare in the Miller Range nakhlites, it appears that SO₄^2?, possibly along with some of the Na⁺, K⁺, and Ca⁺ in these phases, was sourced from wind‐blown sea spray and biogenic emissions from the southern ocean. Cl enrichment in the terrestrially derived “iddingsite” of MIL 05031 and MIL 03346, and the presence of halite at the exterior edge of MIL 090032, can also be explained by this process. However, jarosite within and around the olivine‐bound melt inclusions of MIL 090136 is present in the interior of the meteorite and, therefore, is probably the product of preterrestrial weathering on Mars.     

Petrology and oxygen isotopic compositions of clasts in HED polymict breccia NWA 5232

Northwest Africa (NWA) 5232, an 18.5 kg polymict eucrite, comprises eucritic and exogenic CM carbonaceous chondrite clasts within a clastic matrix. Basaltic clasts are the most abundant eucritic clast type and show a range of textures and grain size, from subophitic to granoblastic. Other eucritic clast types present include cumulate (high‐En pyroxene), pyroxene‐lath, olivine rich with symplectite intergrowths as a break‐down product of a quickly cooled Fe‐rich metastable pyroxferroite, and breccia (fragments of a previously consolidated breccia) clasts. A variable cooling rate and degree of thermal metamorphism, followed by a complex brecciation history, can be inferred for the clasts based on clast rounding, crystallization (and recrystallization) textures, pyroxene major and minor element compositions, and pyroxene exsolution. The range in δ¹⁸O of clasts and matrix of NWA 5232 reflects its origin as a breccia of mixed clasts dominated by eucritic lithologies. The oxygen isotopic compositions of the carbonaceous chondrite clasts identify them as belonging to CM group and indicate that these clasts experienced a low degree of aqueous alteration while part of their parent body. The complex evolutionary history of NWA 5232 implies that large‐scale impact excavation and mixing was an active process on the surface of the HED parent body, likely 4 Vesta.     

Mineralogy of Antarctic basaltic shergottite Queen Alexandra Range 94201: Similarities to Elephant Moraine A79001 (Lithology B) martian meteorite

Abstract— Antarctic meteorite QUE 94201 is a new basaltic shergottite that is mainly composed of subequal amounts of maskelynite and pyroxenes (pigeonite and augite) plus abundant merrillite and accessory phases. It also contains impact melt. Complex zoning patterns in QUE 94201 pyroxenes revealed by elemental map analyses using an electron microprobe suggest a crystallization sequence from Mg-rich pigeonite (En₆₂Fss₃₀Wo_g) to extremely Fe-rich pigeonite (En₅Fs₈₁Wo₁₄) via {110} Mg-rich augite bands (En₄₄Fs₂₀Wo₃₆) in a single crystal. These textures, along with the abundant plagioclase (maskelynite), indicates single-stage rapid cooling (>5 °C/year) of this rock from a supercooled magma. Transition from Mg-rich augite to Fe-rich pigeonite reflects the onset of plagioclase crystallization. Enrichment of late-stage phases in QUE 94201 implies crystallization from an evolved magma and suggests a different parent magma composition from the other basaltic shergottites. Lithology B of EETA79001 basaltic shergottite contains pyroxenes that show complex zoning with augite bands similar to those in QUE 94201 pyroxene, which suggests similar one-stage rapid cooling. Lithology B of EETA79001 also resembles QUE 94201 in its coarse-grained texture of silicates and its high abundance of maskelynite, although QUE 94201 probably crystallized from a more fractionated magma. We also note that some Apollo lunar mare basalts (e.g., 12020 and 12021) have similar mineralogy and petrology to QUE 94201, especially in pyroxene zoning. All these basaltic rocks with complex pyroxene zoning suggest rapid metastable crystallization from supercooled magmas.     

Petrology and trace element geochemistry of Tissint,the newest shergottite fall

The fall and recovery of the Tissint meteorite in 2011 created a rare opportunity to examine a Martian sample with a known, short residence time on Earth. Tissint is an olivine‐phyric shergottite that accumulated olivine antecrysts within a single magmatic system. Coarse olivine grains with nearly homogeneous cores of Mg# >80 suggest slow re‐equilibration. Many macroscopic features of this sample resemble those of LAR 06319, including the olivine crystal size distribution and the presence of evolved oxide and olivine compositions. Unlike LAR 06319, however, no magmatic hydrous phases were found in the analyzed samples of Tissint. Minor and trace element compositions indicate that the meteorite is the product of closed‐system crystallization from a parent melt derived from a depleted source, with no obvious addition of a LREE‐rich (crustal?) component prior to or during crystallization. The whole‐rock REE pattern is similar to that of intermediate olivine‐phyric shergottite EETA 79001 lithology A, and could also be approximated by a more olivine‐rich version of depleted basaltic shergottite QUE 94201. Magmatic oxygen fugacities are at the low end of the shergottite range, with log fO₂ of QFM‐3.5 to ‐4.0 estimated based on early‐crystallized minerals and QFM‐2.4 estimated based on the Eu in pyroxene oxybarometer. These values are similarly comparable to other depleted shergottites, including SaU 005 and QUE 94201. Tissint occupies a previously unsampled niche in shergottite chemistry: containing olivines with Mg# >80, resembling the enriched olivine‐phyric shergottite LAR 06319 in its crystallization path, and comparable to intermediate olivine‐phyric shergottite EETA 79001A, depleted olivine‐phyric shergottite DaG 476, and depleted basaltic shergottite QUE 94201 in its trace element abundances and oxygen fugacity. The apparent absence of evidence for terrestrial alteration in Tissint (particularly in trace element abundances in the whole‐rock and individual minerals) confirms that exposure to the arid desert environment results in only minimal weathering of samples, provided the exposure times are brief.     

Metamorphic diogenite Grosvenor Mountains 95555: Mineral chemistry of orthopyroxene and spinel and comparisons to the diogenite suite

Abstract— Grosvenor Mountains (GRO) 95555 is a relatively newly discovered and unique metamorphic diogenite. It does not show the usual brecciated appearance of other diogenites or wide compositional variability of orthopyroxene or spinel. Electron microprobe analysis (EMPA) and secondary ion mass spectrometer (SIMS) analysis of orthopyroxene and EMPA of spinel show limited compositional variability. Compositions for orthopyroxene for Fe/(Fe + Mg) atomic, Al, Zr, Y, and Yb fall in the middle of the compositional ranges of the diogenite suite. Apparently, GRO 95555 formed at sufficient depth or location to escape brecciation by meteorite bombardment and in a thermal regime that led to high‐grade metamorphism resulting in homogeneous mineral compositions.     

Petrology,chemistry, and isotopic compositions of the lunar highland regolith breccia Dar al Gani 262

Abstract— Lunar meteorite Dar al Gani 262 (DG 262)—found in the Libyan part of the Sahara—is a mature, anorthositic regolith breccia with highland affinities. The origin from the Moon is undoubtedly indicated by its bulk chemical composition; radionuclide concentrations; noble gas, N, and O isotopic compositions; and petrographic features. Dar al Gani 262 is a typical anorthositic highland breccia similar in mineralogy and chemical composition to Queen Alexandra Range (QUE) 93069. About 52 vol% of the studied thin sections of Dar al Gani 262 consist of fine-grained(100 μm) constituents, and 48 vol% is mineral and lithic clasts and impact-melt veins. The most abundant clast types are feldspathic fine-grained to microporphyritic crystalline melt breccias (50.2 vol%; includes recrystallized melt breccias), whereas mafic crystalline melt breccias are extremely rare (1.4 vol%). Granulitic lithologies are 12.8 vol%, intragranularly recrystallized anorthosites and cataclastic anorthosites are 8.8 and 8.2 vol%, respectively, and (devitrified) glasses are 2.7 vol%. Impact-melt veins (5.5 vol% of the whole thin sections) cutting across the entire thin section were probably formed subsequent to the lithification process of the bulk rock at pressures below 20 GPa, because the bulk rock never experienced a higher peak shock pressure. Mafic crystalline melt breccias are very rare in Dar al Gani 262 and are similar in abundance to those in QUE 93069. The extremely low abundance of mafic components and the bulk composition may constrain possible areas of the Moon from which the breccia was derived. The source area of Dar al Gani 262 must be a highland terrain lacking significant mafic impact melts or mare components. On the basis of radionuclide activities, an irradiation position of DG 262 on the Moon at a depth of 55–85 g/cm³and a maximum transit time to Earth <0.15 Ma is suggested. Dar al Gani 262 contains high concentrations of solar-wind-implanted noble gases. The isotopic abundance ratio ⁴⁰Ar/³⁶Ar < 3 is characteristic of lunar soils. The terrestrial weathering of DG 262 is reflected by the occurrence of fractures filled with calcite and by high concentrations of Ca, Ba, Cs, Br, and As. There is also a large amount of terrestrial C and some N in the sample, which was released at low temperatures during stepped heating. High concentrations of Ni, Co, and Ir indicate a significant meteoritic component in the lunar surface regolith from which DG 262 was derived.     

Ni/S/Cl systematics and the origin of impact‐melt glasses in Martian meteorite Elephant Moraine 79001

Martian meteorite Elephant Moraine A79001 (EET 79001) has received considerable attention for the unusual composition of its shock melt glass, particularly its enrichment in sulfur relative to the host shergottite. It has been hypothesized that Martian regolith was incorporated into the melt or, conversely, that the S‐enrichment stems from preferential melting of sulfide minerals in the host rock during shock. We present results from an electron microprobe study of EET 79001 including robust measurements of major and trace elements in the shock melt glass (S, Cl, Ni, Co, V, and Sc) and minerals in the host rock (Ni, Co, and V). We find that both S and major element abundances can be reconciled with previous hypotheses of regolith incorporation and/or excess sulfide melt. However, trace element characteristics of the shock melt glass, particularly Ni and Cl abundances relative to S, cannot be explained either by the incorporation of regolith or sulfide minerals. We therefore propose an alternative hypothesis whereby, prior to shock melting, portions of EET 79001 experienced acid‐sulfate leaching of the mesostasis, possibly groundmass feldspar, and olivine, producing Al‐sulfates that were later incorporated into the shock melt, which then quenched to glass. Such activity in the Martian near‐surface is supported by observations from the Mars Exploration Rovers and laboratory experiments. Our preimpact alteration model, accompanied by the preferential survival of olivine and excess melting of feldspar during impact, explains the measured trace element abundances better than either the regolith incorporation or excess sulfide melting hypothesis does.     

Petrology and provenance of a very‐low‐titanium picrite clast in lunar highland regolith breccia 15295

Clast 100 in regolith breccia 15295 could be a key to resolving the relationship(s) between mare basalts and lunar picritic glasses. The clast is basaltic, with texture, mineralogy, mineral compositions, and calculated bulk composition suggesting that it crystallized in a thick lava flow or shallow intrusive body from a very‐low‐titanium (VLT) basaltic magma. The estimated bulk composition of clast 15295,100 is primitive (i.e., magnesian) compared to those of known VLT basalts, and is very close to those of VLT picritic green glasses, especially the Apollo 14 A green glass. From these similarities, we infer that clast 15295,100 is a crystalline product of a picritic magma similar to the Apollo 14 A glass. Clementine and M³ remotely sensed data of the lunar surface were used to find areas that have chemical compositions consistent with those of clast 15295,100, not only near the Apollo 15 site, but in a broad region surrounding the site. Two regions are consistent with clast's 15295,100 compositional data. The larger region is in southern Mare Imbrium, and a smaller region is in the eastern half of Sinus Aestuum. These locations should be considered as candidates for future missions focusing on sample science.     

40Ar‐39Ar age determinations of lunar basalt meteorites Asuka 881757, Yamato 793169, Miller Range 05035, La Paz Icefield 02205, Northwest Africa 479, and basaltic breccia Elephant Moraine 96008

Abstract— ⁴⁰Ar‐³⁹Ar data are presented for the unbrecciated lunar basaltic meteorites Asuka (A‐) 881757, Yamato (Y‐) 793169, Miller Range (MIL) 05035, LaPaz Icefield (LAP) 02205, Northwest Africa (NWA) 479 (paired with NWA 032), and basaltic fragmental breccia Elephant Moraine (EET) 96008. Stepped heating ⁴⁰Ar‐³⁹Ar analyses of several bulk fragments of related meteorites A‐881757, Y‐793169 and MIL 05035 give crystallization ages of 3.763 ± 0.046 Ga, 3.811 ± 0.098 Ga and 3.845 ± 0.014 Ga, which are comparable with previous age determinations by Sm‐Nd, U‐Pb Th‐Pb, Pb‐Pb, and Rb‐Sr methods. These three meteorites differ in the degree of secondary ⁴⁰Ar loss with Y‐793169 showing relatively high Ar loss probably during an impact event ?200 Ma ago, lower Ar loss in MIL 05035 and no loss in A‐881757. Bulk and impact melt glass‐bearing samples of LAP 02205 gave similar ages (2.985 ± 0.016 Ga and 2.874 ± 0.056 Ga) and are consistent with ages previously determined using other isotope pairs. The basaltic portion of EET 96008 gives an age of 2.650 ± 0.086 Ga which is considered to be the crystallization age of the basalt in this meteorite. The Ar release for fragmental basaltic breccia EET 96008 shows evidence of an impact event at 631 ± 20 Ma. The crystallization age of 2.721 ± 0.040 Ga determined for NWA 479 is indistinguishable from the weighted mean age obtained from three samples of NWA 032 supporting the proposal that these meteorites are paired. The similarity of ⁴⁰Ar‐³⁹Ar ages with ages determined by other isotopic systems for multiple meteorites suggests that the K‐Ar isotopic system is robust for meteorites that have experienced a significant shock event and not a prolonged heating regime.     

Mixing relations of the howardite‐eucrite‐diogenite suite: A new statistical approach of independent component analysis for the Dawn mission

Dawn has recently revealed that the surface of Vesta is heterogeneously covered by polymictic regoliths represented by mixtures of howardite, eucrite, and diogenite (HED) meteorites. Mixing relations of the HED suite are examined here using a new computational statistical approach of independent component analysis (ICA). We performed eight‐component ICA (Si, Ti, Al, Cr, Fe, Mn, Mg, and Ca) for 209 HED bulk‐rock compositions. The ICA results indicate that the HED bulk‐rock compositions can be reduced into three independent components (IC) and these IC vectors can reasonably explain compositional variation, petrographic observations, and the mixing relations of the HED suite. The IC‐1 vector represents a eucrite variation that extends from cumulate eucrite toward main‐group (MG) and incompatible‐element enriched eucrites. The IC‐2 vector represents a compositional variation of howardites that extends from diogenites to MG‐eucrites, indicating the well‐known two‐component mixing trend of diogenite and eucrite. The IC‐3 vector represents a compositional variation defined by diogenites and olivine‐bearing diogenites, suggesting mixing of olivine and orthopyroxene. Among the three ICs, the diogenite‐eucrite mixing trend IC‐2 is most statistically robust and dominates the compositional variations of the HED suite. Our ICA study further indicates that the combination of only three elements (Mg, Si, and Fe) approximates the eight‐component ICA model, and that the limited number of resolvable γ‐ray spectra obtained by the Dawn mission possibly discriminates olivine lithologies from the olivine‐free regolith breccias on the surface of Vesta.