The igneous crystallization history of an ancient Martian meteorite from rare earth element microdistributions

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.     

Determination of parental magmas of HED cumulates: The effects of interstitial melts

Abstract— An evaluation of trapped melts effects during crystallization and subsolidus equilibration of cumulates is necessary to constrain the composition of their parental magmas. In this paper, a simple mass balance approach is described. It allows estimation of trace element abundances in these parental melts from phase compositions. It is used to discuss the genesis of cumulate eucrites and diogenites. The REE behavior is in full agreement with the view that cumulate eucrites formed from melts similar to noncumulate eucrites. Trapped melt fractions ranging from <10 wt% for Moama to ?30 wt% for Moore County were involved. The origin of diogenites is more complex. The assumption that eucrites and diogenites shared the same parental melts cannot satisfactorily explain the diversity of incompatible trace element ratios (e.g., Dy/Yb) observed in diogenitic orthopyroxenes, even if interstitial melt effects are taken into account. Moreover, some diogenites unambiguously crystallized from magmas displaying significant HREE (heavy rare earth elements) enrichments. More likely, diogenites formed from distinct batches of parental magmas, as previously proposed by Mittlefehldt (1994), Fowler et al. (1995), and Shearer (1997).     

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‰).     

Geochemistry of diogenites: Still more diversity in their parental melts

Abstract— We report on the major and trace element abundances of 18 diogenites, and O‐isotopes for 3 of them. Our analyses extend significantly the diogenite compositional range, both in respect of Mg‐rich (e.g., Meteorite Hills [MET] 00425, MgO = 31.5 wt%) and Mg‐poor varieties (e.g., Dhofar 700, MgO = 23 wt%). The wide ranges of siderophile and chalcophile element abundances are well explained by the presence of inhomogeneously distributed sulfide or metal grains within the analyzed chips. The behavior of incompatible elements in diogenites is more complex, as exemplified by the diversity of their REE patterns. Apart from a few diogenite samples that contain minute amounts of phosphate, and whose incompatible element abundances are unlike the orthopyroxene ones, the range of incompatible element abundances, and particularly the range of Dy/Yb ratios in diogenites is best explained by the diversity of their parental melts. We estimate that the FeO/MgO ratios of the diogenite parental melts range from about 1.4 to 3.5 and therefore largely overlap the values obtained for non‐cumulate eucrites. Our results rule out the often accepted view that all the diogenites formed from parental melts more primitive than eucrites during the crystallization of a magma ocean. Instead, they point to a more complex history, and suggest that diogenites were derived from liquids produced by the remelting of cumulates formed from the magma ocean.     

GENESIS OF THE CUMULATE EUCRITES SERRA DE MAGÉ AND MOORE COUNTY: A GEOCHEMICAL STUDY

Major, minor and trace element abundances have been determined by instrumental neutron activation analysis (INAA) in whole rock and plagioclase separates of Serra de Magé (SdM). The whole rock contains 52% normative plagioclase and its chondritic normalized REE abundance pattern shows a large Eu anomaly, dominated by the plagioclase REE distribution, and nearly unfractionated La-Sm and Sm-Lu abundances. The plagioclase separates contained ～ 6% pyroxenes and exhibited a typical plagioclase REE distribution. The REE abundances in the derivative equilibrium magmas from which SdM and Moore County (MC) plagioclases crystallized have been estimated from the plagioclase data and the plagioclase mineral/liquid partition coefficients. The REE distributions in possibly earlier parental magmas were calculated by assuming that various degrees of plagioclase and pigeonite (plagioclase/pigeonite = 1) fractional crystallization had been operative prior to the crystallization of SdM and MC. The calculated La/Sm and Sm/Yb ratios for the earlier magmas are essentially the same as the equilibrium magmas over a wide range (10–95%) of the assumed fractional crystallization. Considering the REE distributions and the Fe/Fe+Mg ratios, calculation shows that there is no simple genetic relationship between MC and SdM via fractional crystallization processes. A hypothesis for the derivation of these cumulate eucrites in the plutonic environment from residual diogenitic liquid, which was produced by the extensive partial melting of an eucritic source material followed by the crystallization of diogenite, also fails to account for the fractionated REE patterns calculated for the equilibrium and the possible parental magmas for either SdM or MC. Equilibrium non-modal partial melting calculations indicate that SdM and MC could be genetically related by a factor ～ 6 difference in the degrees of partial melting from a similar source material. However, this common source material which should contain > 30% high-Ca clinopyroxene and has a chondritic normalized La/Yb ～ 3, is different than that proposed for the non-cumulate eucrites.     

KREEP basalt petrogenesis: Insights from 15434,181

Returned lunar KREEP basalts originated through impact processes or endogenous melting of the lunar interior. Various methods have been used to distinguish between these two origins, with varying degrees of success. Apollo 15 KREEP basalts are generally considered to be endogenous melts of the lunar interior. For example, sample 15434,181 is reported to have formed by a two‐stage cooling process, with large orthopyroxene (Opx) phenocrysts forming first and eventually cocrystalizing with smaller plagioclase crystals. However, major and trace element analyses of Opx and plagioclase coupled with calculated equilibrium liquids are inconsistent with the large orthopyroxenes being a phenocryst phase. Equilibrium liquid rare earth element (REE) profiles are enriched relative to the whole rock (WR) composition, inconsistent with Opx being an early crystallizing phase, and these are distinct from the plagioclase REE equilibrium liquids. Fractional crystallization modeling using the Opx equilibrium liquids as a parental composition cannot reproduce the WR values even with crystallization of late‐stage phosphates and zircon. This work concludes that instead of being a phenocryst phase, the large Opx crystals are actually xenocrysts that were subsequently affected by pyroxene overgrowths that formed intergrowths with cocrystallizing plagioclase.     

RARE EARTH ELEMENT ABUNDANCES IN SEPARATED PHASES OF MAYO BELWA,AN ENSTATITE ACHONDRITE

Separated fractions from the Mayo Belwa aubrite have been analysed for the rare earth elements (REE). The data show no ytterbium anomalies but the feldspar and magnetic fractions show complementary europium anomalies. The separated phases together account for the total REE abundances in the bulk meteorite which are about 0.5 times chondritic. The REE content of the feldspar is greater than that of the bulk meteorite. The partition coefficients for the REE between feldspar and orthopyroxene are about 10 times (in favour of the feldspar) those of the nearest equivalent terrestrial feldspar/orthopyroxene pairs, implying that the distribution of the REE which would result from equilibrium co-crystallisation from a single liquid has been disturbed by a later event. This occurred more recently than 4.33 b.y. ago and resulted in a redistribution of the REE between the feldspar and a REE enriched residue. However, the REE patterns of the minerals are very like those of terrestrial equivalents and appear to be the result of igneous cumulus processes on a parent body rather than condensation of dust from a nebular gas.     

Northwest Africa 011: A “eucritic” basalt from a non‐eucrite parent body

Abstract— We have carried out a detailed petrographic, mineralogical, and trace element study of Northwest Africa (NWA) 011. This meteorite bears many similarities to the eucrites it was initially identified with, although oxygen isotopic compositions rule out a genetic relationship. Like many eucrites, NWA 011 crystallized from a source with approximately chondritic proportions of REE, although a slightly LREE‐enriched bulk composition with a small positive Eu anomaly, as well as highly fractionated Fe/Mg ratios and depleted Sc abundances (Korotchantseva et al. 2003), suggest that the NWA 011 source experienced some pyroxene and/or olivine fractionation. Thermal metamorphism resulted in homogenization of REE abundances within grains, but NWA 011 did not experience the intergrain REE redistribution seen in some highly metamorphosed eucrites. Despite a similarity in oxygen isotopic compositions, NWA 011 does not represent a basaltic partial melt from the acapulcoite/lodranite parent body. The material from which NWA 011 originated may have been like some CH or CB chondrites, members of the CR chondrite clan, which are all related through oxygen isotopic compositions. The NWA 011 parent body is probably of asteroidal origin, possibly the basaltic asteroid 1459 Magnya.     

Complexities on the acapulcoite‐lodranite parent body: Evidence from trace element distributions in silicate minerals

Abstract— The trace element distributions of individual minerals from seven acapulcoites and lodranites have been studied. Systematic differences are evident between some members of the two groups. Specifically, pyroxenes from the lodranites MacAlpine Hills (MAC) 88177 and Lewis Cliff (LEW) 88280 exhibit depletions of the rare earth elements (REE) and other incompatible trace elements (Ti, Zr, Y), relative to acapulcoite (Acapulco, Allan Hills (ALH) A81261) pyroxenes, that are consistent with the formation and removal of 15% or more silicate partial melts from these meteorites. Phosphate REE patterns in these lodranites also support this scenario. However, other members of the acapulcoite‐lodranite clan exhibit more complex trace element variations. Elephant Moraine (EET) 84302, which has been classified as transitional between the acapulcoites and lodranites, generally has trace element characteristics similar to the acapulcoites. However, its plagioclase REE compositions suggest a somewhat greater degree of metamorphism than that experienced by acapulcoites such as Acapulco and ALHA81261. Similar and elevated REE abundances in the silicate phases from acapulcoite ALHA81187 and lodranite Graves Nunataks (GRA) 95209 suggest that these two meteorites, in fact, experienced similar thermal histories. This probably included some silicate partial melting, although little melt appears to have been lost from the samples. The observed variations in the trace element abundances of these samples from the acapulcoite‐lodranite clan emphasize the complex and varied processes that have acted on their parent body. The simple bimodal classification of these meteorites based primarily on petrographic criteria, which has been used to date, appears to be inadequate to describe this diverse group of samples, as they represent a range of degrees of partial melting, both with and without accompanying melt migration. In some instances, secondary processes on the parent body, such as cryptic metasomatism, have further modified sample compositions.     

Geochemistry of intermediate olivine‐phyric shergottite Northwest Africa 6234, with similarities to basaltic shergottite Northwest Africa 480 and olivine‐phyric shergottite Northwest Africa 2990

Abstract— The newly found meteorite Northwest Africa 6234 (NWA 6234) is an olivine (ol)‐phyric shergottite that is thought, based on texture and mineralogy, to be paired with Martian shergottite meteorites NWA 2990, 5960, and 6710. We report bulk‐rock major‐ and trace‐element abundances (including Li), abundances of highly siderophile elements, Re‐Os isotope systematics, oxygen isotope ratios, and the lithium isotope ratio for NWA 6234. NWA 6234 is classified as a Martian shergottite, based on its oxygen isotope ratios, bulk composition, and bulk element abundance ratios, Fe/Mn, Al/Ti, and Na/Al. The Li concentration and δ⁷Li value of NWA 6234 are similar to that of basaltic shergottites Zagami and Shergotty. The rare earth element (REE) pattern for NWA 6234 shows a depletion in the light REE (La‐Nd) compared with the heavy REE (Sm‐Lu), but not as extreme as the known “depleted” shergottites. Thus, NWA 6234 is suggested to belong to a new category of shergottite that is geochemically “intermediate” in incompatible elements. The only other basaltic or ol‐phyric shergottite with a similar “intermediate” character is the basaltic shergottite NWA 480. Rhenium‐osmium isotope systematics are consistent with this intermediate character, assuming a crystallization age of 180 Ma. We conclude that NWA 6234 represents an intermediate compositional group between enriched and depleted shergottites and offers new insights into the nature of mantle differentiation and mixing among mantle reservoirs in Mars.     

The composition and thickness of the crust of Mars estimated from rare earth elements and neodymium-isotopic compositions of Martian meteorites

Abstract— Isotopic and trace element compositions of Martian meteorites show that early differentiation of Mars produced complementary crustal and mantle reservoirs that were sampled by later magmatic events. This paper describes a mass balance model that estimates the rare earth element (REE) content and thickness of the crust of Mars from the compositions of shergottites. The diverse REE and Nd isotopic compositions of shergottites are most easily explained by variable addition of light rare earth element (LREE)–enriched crust to basaltic magmas derived from LREE-depleted mantle source regions. Antarctic shergottites EET 79001, ALH 77005, LEW 88516, and QUE 94201 all have strongly LREE-depleted patterns and positive initial ¹⁴³Nd isotopic compositions, which is consistent with the generation of these magmas from depleted mantle sources and little or no interaction with enriched crust. In contrast, Shergotty and Zagami have negative initial ¹⁴³Nd isotopic compositions and less pronounced depletions of the LREE, which have been explained by incorporation of enriched crustal components into mantle-derived magmas (Jones, 1989; Longhi, 1991; Borg et al., 1997). The mass balance model presented here derives the REE composition of the crustal component in Shergotty by assuming it represents a mixture between a mantle-derived magma similar in composition to EET 79001A and a LREE-enriched crustal component. The amount of crust in Shergotty is constrained by mixing relations based on Nd-isotopic compositions, which allows the REE pattern of the crustal component to be calculated by mass balance. The effectiveness of this model is demonstrated by the successful recovery of important characteristics of the Earth's continental crust from terrestrial Columbia River basalts. Self-consistent results for Nd-isotopic compositions and REE abundances are obtained if Shergotty contains ～10–30% of LREE-enriched crust with >10 ppm Nd. This crustal component would have moderately enriched LREE (Sm/Nd = 0.25–0.27; ¹⁴⁷Sm/¹⁴⁴Nd = 0.15–0.17; La/Yb = 2.7–3.8), relatively unfractionated heavy rare earth elements (HREE), and no Eu anomaly. Crust with these characteristics can be produced from a primitive lherzolitic Martian mantle by modest amounts (2–8%) of partial melting, and it would have a globally averaged thickness of <45 km, which is consistent with geophysical estimates. Mars may serve as a laboratory to investigate planetary differentiation by extraction of a primary basaltic crust.     

Partitioning of Rare Earth Elements Between Hibonite and Melt and Implications for Nebular Condensation of the Rare Earth Elements

Abstract— The partitioning of the rare earth elements (REE) between hibonite and silicate melt has been investigated at 1470 °C in the system calcium tschermak's molecule-diopside. Oxygen fugacity was varied between air and the iron-wustite buffer using conventional gas mixing, and to “infinitely reducing” using Sr²⁺ as a surrogate for Eu²⁺. The partition coefficient (D) pattern is light REE enriched with D(La) = 7.15 and D(Yb) = 0.1. D(Eu) varied from about 2 in air to about 0.55 in an “infinitely reducing” atmosphere. Experiments were reversed for Eu and, by implication, a close approach to equilibrium was achieved for other elements. Absolute activity coefficients for REE in hibonite were estimated, yielding γ_La = 330, γ_Eu3+ = 1200, and γ_Yb = 24 000. These results suggest that unless the principal phase(s) into which a trace element is dissolving and the activity—composition relationships for that trace element in that phase(s) are known, condensation temperatures based on assumed ideal solution behavior will generally be in error.     

Microdistributions and petrogenetic implications of rare earth elements in polymict ureilites

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.     

A petrogenetic model for the origin and compositional variation of the martian basaltic meteorites

Abstract— The major element, trace element, and isotopic compositional ranges of the martian basaltic meteorite source regions have been modeled assuming that planetary differentiation resulted from crystallization of a magma ocean. The models are based on low to high pressure phase relationships estimated from experimental runs and estimates of the composition of silicate Mars from the literature. These models attempt to constrain the mechanisms by which the martian meteorites obtained their superchondritic CaO/Al₂O₃ ratios and their source regions obtained their parent/daughter (⁸⁷Rb/⁸⁶Sr, ¹⁴⁷Sm/¹⁴⁴Nd, and ¹⁷⁶Lu/¹⁷⁷Hf) ratios calculated from the initial Sr, Nd, and Hf isotopic compositions of the meteorites. High pressure experiments suggest that majoritic garnet is the liquidus phase for Mars relevant compositions at or above 12 GPa. Early crystallization of this phase from a martian magma ocean yields a liquid characterized by an elevated CaO/Al₂O₃ ratio and a high Mg#. Olivine‐pyroxene‐garnet‐dominated cumulates that crystallize subsequently will also be characterized by superchondritic CaO/Al₂O₃ ratios. Melting of these cumulates yields liquids with major element compositions that are similar to calculated parental melts of the martian meteorites. Furthermore, crystallization models demonstrate that some of these cumulates have parent/daughter ratios that are similar to those calculated for the most incompatible‐element‐depleted source region (i.e., that of the meteorite Queen Alexandra [QUE] 94201). The incompatible‐element abundances of the most depleted (QUE 94201‐like) source region have also been calculated and provide an estimate of the composition of depleted martian mantle. The incompatible‐element pattern of depleted martian mantle calculated here is very similar to the pattern estimated for depleted Earth's mantle. Melting the depleted martian mantle composition reproduces the abundances of many incompatible elements in the parental melt of QUE 94201 (e.g., Ba, Th, K, P, Hf, Zr, and heavy rare earth elements) fairly well but does not reproduce the abundances of Rb, U, Ta and light rare earth elements. The source regions for meteorites such as Shergotty are successfully modeled as mixtures of depleted martian mantle and a late stage liquid trapped in the magma ocean cumulate pile. Melting of this hybrid source yields liquids with major element abundances and incompatible‐element patterns that are very similar to the Shergotty bulk rock.     

Experimental petrology,crystallization history,and parental magma characteristics of olivine‐phyric shergottite NWA 1068: Implications for the petrogenesis of “enriched” olivine‐phyric shergottites

Abstract– Northwest Africa (NWA) 1068 is one of the few olivine‐phyric shergottites (e.g., NWA 1068, Larkman Nunatak [LAR] 06319, and Roberts Massif [RBT] 04262) that is not depleted in light rare earth elements (LREE). Its REE pattern is similar to that of the basaltic shergottite Shergotty, suggesting a possible connection between the olivine‐phyric and the basaltic shergottites. To test this possible link, we have investigated the high‐pressure near‐liquidus phase equilibria for the NWA 1068 meteorite bulk composition. Our results show that the NWA 1068 bulk composition does not represent an unmodified mantle‐derived melt; the olivine and pyroxene in our near‐liquidus experiments are more magnesian than in the rock itself, which suggests that NWA 1068 contains cumulate minerals (extra olivine). We have then used these experimental results combined with the pyroxene compositions in NWA 1068 to constrain the possible high‐pressure crystallization history of the parental magma. These results suggest that NWA 1068 had a complex polybaric history. Finally, we have calculated a model parental magma composition for the NWA 1068 meteorite. The calculated parental magma is an evolved basaltic composition which is too ferroan to be a primitive melt directly derived from the mantle. We suggest that it ponded and crystallized at approximately the base of the crust. This provided an opportunity for the magma to become contaminated by an “enriched” crustal component prior to crystallization. The results and modeling from these experiments are applicable not only to the NWA 1068 meteorite, but also to LAR 06319 and possibly any other enriched olivine‐phyric shergottite.     

Thermal histories of angrite meteorites: Trace element partitioning among silicate minerals in Angra dos Reis,Lewis Cliff 86010, and experimental analogs

Abstract— We measured rare earth element (REE) abundances in selected silicate phases in the angrites Angra dos Reis (AdoR) and Lewis Cliff (LEW) 86010 in order to further clarify the thermal history of AdoR. We also carried out a preliminary experimental study designed to examine apparent REE partitioning between silicates (fassaite, olivine, kirschsteinite, and melt) in synthetic analogs of angrites under disequilibrium conditions at liquidus temperatures. Silicates in AdoR are homogeneous with respect to major, minor, and trace elements, which is consistent with the interpretation that AdoR underwent extensive subsolidus equilibration. REE distributions in olivine and kirschsteinite in AdoR are similar to those in LEW 86010 and are consistent with the formation of kirschsteinite by exsolution from olivine during cooling and/or annealing. There is no evidence for a disequilibrium trace element signature that could have been inherited from rapid cooling at liquidus temperatures. This is supported by our petrographic observations of the occurrence of kirschsteinite within olivine aggregates in AdoR. Olivine/kirschsteinite pairs in AdoR record closure temperatures around 600–650 °C.     

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 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.     

Chemical and isotopic constraints on the formation and crystallization of SA-1, a basaltic Allende plagioclase-olivine inclusion

Abstract— SA-1, an unusual basaltic plagioclase-olivine inclusion (POI) in Allende, has concentric textural and mineralogic zones, a fine-grained, 100μm outer border and a coarse-grained interior with subophitic texture. Fassaite, diopside and olivine from the exterior border and interior of SA-1 have uniform intrinsic mass fractionation with isotopically heavy Mg (F_Mg = 3.6 ± 1.8‰/amu). In contrast, spinels from the spinel-rich regions adjacent to the fine-grained border have normal Mg isotopic composition (F_Mg = 0.1 ± 1.5‰/amu). The cores of large calcic (An_90,99) plagioclase have no excess ²⁶Mg, corresponding to ²⁶Mg*/ ²⁷Al < 3.7 × 10^?6. The Mg isotopic heterogeneity in SA-1 requires initial cooling rates of spinel-rich regions adjacent to the fine-grained border to be greater than ～75 °C/hr. In contrast, the subophitic texture of the interior suggests cooling rates of 5–20 °C/ hr. The minerals in SA-1 exhibit a wide range of REE abundances. Lanthanum concentrations vary from 1 × chondritic (ch) in early crystallizing diopside to 100 × ch in late crystallizing fassaite. Nepheline has 18–20 × ch LREE and 11–25 × ch HREE and iron-rich mesostasis is highly enriched in the REE with 270–400 × ch LREE and 230–280 × ch HREE. The complementary REE patterns of clinopyroxene and plagioclase and the enrichment of incompatible trace elements in the mesostasis and late crystallizing phases is consistent with closed system crystallization. The REE data for nepheline and the iron-rich mesostasis indicate these phases are in equilibrium and that nepheline crystallized from a melt. Influx of alkalies, minor Fe and halogens must have occurred during the last stages of crystallization or the inclusion must have been partially molten during Na influx as both anorthite (An₉₉) and nepheline are present in this inclusion. The preservation of isotopic heterogeneity in an inclusion that crystallized from a melt implies that melting was incomplete, allowing for survival of the relict spinels. The major and trace element abundances in SA-1 are inconsistent with formation as a mixture of nebular materials and suggest that SA-1 contains a chemically fractionated component produced by igneous differentiation.     

Paired nakhlites MIL 090030, 090032, 090136, and 03346: Insights into the Miller Range parent meteorite

Abstract– Miller Range (MIL) 03346 is the most oxidized and least equilibrated nakhlite known and displays the highest amount of intercumulus phase. The discovery of three new nakhlites, MIL 090030, MIL 090032, and MIL 090136, in the Miller Range, Antarctica, geographically close to the location of MIL 03346, suggests that they may come from the same parent meteorite. In this study, we investigate the mineralogy and texture of cumulus and intercumulus phases, in situ major and trace element compositions for the cumulus phases, as well as pyroxene crystal size distribution patterns and spatial distribution patterns of MIL 090030, 090032, and 090136. Using these combined results, we conclude that the three nakhlites studied here are paired with MIL 03346. However, modal mineral abundances of MIL 090030, 090032, 090136, and 03346 exhibit variations indicating that a single sample of a Miller Range nakhlite is not modally representative of the parent meteorite and that analyses of multiple samples for a single nakhlite may be necessary to obtain representative modal data for placement in the cumulate pile. Our calculated parental melt composition based on all the paired samples confirms a previous study suggesting that the nakhlite parent melt crystallized as a closed system.