Northwest Africa 1950: Mineralogy and comparison with Antarctic lherzolitic shergottites

Abstract— NWA 1950 is a new lherzolitic shergottite recently recovered from Morocco and is the first sample of this group found outside Antarctica. Major constituent phases of NWA 1950 are olivine, pyroxenes, and plagioclase glass (“maskelynite”) and the rock shows a two distinct textures: poikilitic and non‐poikilitic typical of lherzolitic shergottites. In poikilitic areas, several‐millimeter‐sized pyroxene oikocrysts enclose cumulus olivine and chromite. In contrast, pyroxenes are much smaller in non‐poikilitic areas, and olivine and plagioclase glass are more abundant. Olivine in non‐poikilitic areas is more Fe‐rich (Fa_29–31) and shows a narrower distribution than that in poikilitic areas (Fa_23–29). Pyroxenes in non‐poikilitic areas are also more Fe‐rich than those in poikilitic areas that show continuous chemical zoning suggesting fractional crystallization under a closed system. These observations indicate that pyroxene in non‐poikilitic areas crystallized from evolved interstitial melts and olivine was re‐equilibrated with such melts. NWA 1950 shows similar mineralogy and petrology to previously known lherzolitic shergottites (ALH 77005, LEW 88516, Y‐793605 and GRV 99027) that are considered to have originated from the same igneous body on Mars. Olivine composition of NWA 1950 is intermediate between those of ALH 77005‐GRV 99027 and those of LEW 88516‐Y‐793605, but is rather similar to ALH 77005 and GRV 99027. The subtle difference of mineral chemistry (especially, olivine composition) can be explained by different degrees of re‐equilibration compared to other lherzolitic shergottites, perhaps due to different location in the same igneous body. Thus, NWA 1950 experienced a high degree of re‐equilibration, similar to ALH 77005 and GRV 99027.     

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.     

Magmatic inclusions and felsic clasts in the Dar al Gani 319 polymict ureilite

Abstract— Magmatic inclusions occur in type II ureilite clasts (olivine‐orthopyroxene‐augite assemblages with essentially no carbon) and in a large isolated plagioclase clast in the Dar al Gani (DaG) 319 polymict ureilite. Type I ureilite clasts (olivine‐pigeonite assemblages with carbon), as well as other lithic and mineral clasts in this meteorite, are described in Ikeda et al.(2000). The magmatic inclusions in the type II ureilite clasts consist mainly of magnesian augite and glass. They metastably crystallized euhedral pyroxenes, resulting in feldspar component‐enriched glass. On the other hand, the magmatic inclusions in the large plagioclase clast consist mainly of pyroxene and plagioclase, with a mesostasis. They crystallized with a composition along the cotectic line between the pyroxene and plagioclase liquidus fields. DaG 319 also contains felsic lithic clasts that represent various types of igneous lithologies. These are the rare components not found in the common monomict ureilites. Porphyritic felsic clasts, the main type, contain phenocrysts of plagioclase and pyroxene, and their groundmass consists mainly of plagioclase, pyroxene, and minor phosphate, ilmenite, chromite, and/or glass. Crystallization of these porphyritic clasts took place along the cotectic line between the pyroxene and plagioclase fields. Pilotaxitic felsic clasts crystallized plagioclase laths and minor interstitial pyroxene under metastable conditions, and the mesostasis is extremely enriched in plagioclase component in spite of the ubiquitous crystallization of plagioclase laths in the clasts. We suggest that there are two crystallization trends, pyroxene‐metal and pyroxene‐plagioclase trends, for the magmatic inclusions and felsic lithic clasts in DaG 319. The pyroxene‐metal crystallization trend corresponds to the magmatic inclusions in the type II ureilite clasts and the pilotaxitic felsic clasts, where crystallization took place under reducing and metastable conditions, suppressing precipitation of plagioclase. The pyroxene‐plagioclase crystallization trend corresponds to the magmatic inclusions in the isolated plagioclase clast and the porphyritic felsic clasts. This trend developed under oxidizing conditions in magma chambers within the ureilite parent body. The felsic clasts may have formed mainly from albite component‐rich silicate melts produced by fractional partial melting of chondritic precursors. The common monomict ureilites, type I ureilites, may have formed by the fractional partial melting of alkali‐bearing chondritic precursors. However, type II ureilites may have formed as cumulates from a basaltic melt.     

Localized shock melting in lherzolitic shergottite Northwest Africa 1950: Comparison with Allan Hills 77005

Abstract— The lherzolitic Martian meteorite Northwest Africa (NWA) 1950 consists of two distinct zones: 1) low‐Ca pyroxene poikilically enclosing cumulate olivine (Fo_70–75) and chromite, and 2) areas interstitial to the oikocrysts comprised of maskelynite, low‐ and high‐Ca pyroxene, cumulate olivine (Fo_68–71) and chromite. Shock metamorphic effects, most likely associated with ejection from the Martian subsurface by large‐scale impact, include mechanical deformation of host rock olivine and pyroxene, transformation of plagioclase to maskelynite, and localized melting (pockets and veins). These shock effects indicate that NWA 1950 experienced an equilibration shock pressure of 35–45 GPa. Large (millimeter‐size) melt pockets have crystallized magnesian olivine (Fo_78–87) and chromite, embedded in an Fe‐rich, Al‐poor basaltic to picro‐basaltic glass. Within the melt pockets strong thermal gradients (minimum 1 °C/μm) existed at the onset of crystallization, giving rise to a heterogeneous distribution of nucleation sites, resulting in gradational textures of olivine and chromite. Dendritic and skeletal olivine, crystallized in the melt pocket center, has a nucleation density (1.0 × 10³ crystals/mm²) that is two orders of magnitude lower than olivine euhedra near the melt margin (1.6 × 10⁵ crystals/mm²). Based on petrography and minor element abundances, melt pocket formation occurred by in situ melting of host rock constituents by shock, as opposed to melt injected into the lherzolitic target. Despite a common origin, NWA 1950 is shocked to a lesser extent compared to Allan Hills (ALH) 77005 (45–55 GPa). Assuming ejection in a single shock event by spallation, this places NWA 1950 near to ALH 77005, but at a shallower depth within the Martian subsurface. Extensive shock melt networks, the interconnectivity between melt pockets, and the ubiquitous presence of highly vesiculated plagioclase glass in ALH 77005 suggests that this meteorite may be transitional between discreet shock melting and bulk rock melting.     

Spinels and oxygen fugacity in olivine‐phyric and lherzolitic shergottites

Abstract— We examine the occurrences, textures, and compositional patterns of spinels in the olivine‐phyric shergottites Sayh al Uhaymir (SaU) 005, lithology A of Elephant Moraine A79001 (EET‐A), Dhofar 019, and Northwest Africa (NWA) 1110, as well as the Iherzolitic shergottite Allan Hills (ALH) A77005, in order to identify spinel‐olivine‐pyroxene assemblages for the determination of oxygen fugacity (using the oxybarometer of Wood [1991]) at several stages of crystallization. In all of these basaltic martian rocks, chromite was the earliest phase and crystallized along a trend of strict Cr‐Al variation. Spinel (chromite) crystallization was terminated by the appearance of pyroxene but resumed later with the appearance of ulvöspinel. Ulvöspinel formed overgrowths on early chromites (except those shielded as inclusions in olivine or pyroxene), retaining the evidence of the spinel stability gap in the form of a sharp core/rim boundary (except in ALH A77005, where subsolidus reequilibration diffused this boundary). Secondary effects seen in chromites include reaction with melt before ulvöspinel overgrowth, reaction with melt inclusions, reaction with olivine hosts (in ALH A77005), and exsolution of ulvöspinel or ilmenite. All chromites experienced subsolidus Fe/Mg reequilibration. Spinel‐olivine‐pyroxene assemblages representing the earliest stages of crystallization in each rock essentially consist of the highest‐Cr#, lowest‐fe# chromites not showing secondary effects plus the most magnesian olivine and equilibrium low‐Ca pyroxene. Assemblages representing the onset of ulvöspinel crystallization consist of the lowest‐Ti ulvöspinel, the most magnesian olivine in which ulvöspinel occurs as inclusions, and equilibrium low‐Ca pyroxene. The results show that, for early crystallization conditions, oxygen fugacity (fO₂) increases from SaU 005 and Dhofar 019 (?QFM ‐3.8), to EET‐A (QFM ‐2.8) and ALH A77005 (QFM ‐2.6), to NWA 1110 (QFM ‐1.7). Estimates for later conditions indicate that in SaU 005 and Dhofar 019 oxidation state did not change during crystallization. In EET‐A, there was an increase in fO₂ that may have been due to mixing of reduced material with a more oxidized magma. In NWA 1110, there was a dramatic increase, indicating a non‐buffered system, possibly related to its high oxidation state. Differences in fO₂ among shergottites are not primarily due to igneous fractionation but, rather, to derivation from (and possibly mixing of) different reservoirs.     

Sulfide mineralogy and redox conditions in some shergottites

Abstract— Magmatic sulfide mineralogy has been studied in 2 olivine‐phyric shergottites (DaG 476 and SaU 005) and 4 basaltic shergottites (Zagami, Shergotty, Los Angeles, and NWA 480). Modal abundances of magmatic sulfides, as estimated by image analysis on thin section, are high (0.16 to 0.53 area percent) and correlate positively with abundances of Fe‐Ti oxides. Sulfides are mesostasis minerals, being mostly interstitial grains or locally enclosed in post‐cumulus melt inclusions (e.g., SaU 005) in olivine. Sulfides in shergottites are composed of major pyrrhotite containing pentlandite exsolutions associated with minor amounts of Cu sulfides (chalcopyrite and/or cubanite). Hot desert finds (e.g., DaG 476) show abundant fracture‐filling iron (oxy)hydroxides of probable terrestrial origin. Unaltered sulfides show metal‐rich hexagonal pyrrhotite compositions with metal/sulfur (M/S) ratio ranging between 0.936 ± 0.005 and 0.962 ± 0.01. This compositional range corresponds to the two‐phase structural domain 2C + nC of the Fe‐S system; however, the high‐temperature disordered hexagonal 1C pyrrhotite structure would be in better agreement with magnetic properties of shergottites. Ni contents in pyrrhotite increase from Los Angeles (<0.05 at%) to Shergotty, Zagami, and NWA 480 (0.2–0.5 at%), and DaG 476 and SaU 005 (up to 3 at%). The higher Ni values of pyrrhotite in olivine‐phyric shergottites correlate with the abundance of pentlandite exsolutions, both reflecting more primitive Ni‐rich sulfide liquids where abundant olivine crystallized. This result and the strong correlation between sulfide abundances and Fe‐Ti oxides argue for a primary magmatic origin of these sulfides. Although they reproduce the trend of magmatic oxygen fugacity conditions determined from Fe‐Ti oxide pairs, observed pyrrhotite compositions are systematically more metal‐deficient compared to those calculated from the Fe‐S‐O system. This suggests post‐magmatic oxidation during cooling on Mars, followed by terrestrial weathering for hot desert finds.     

Rb‐Sr and Sm‐Nd isotopic systematics of the lherzolitic shergottite GRV 99027

Abstract– Rb‐Sr and Sm‐Nd isotopic analyses of the lherzolitic shergottite Grove Mountains (GRV) 99027 are reported. GRV 99027 yields a Rb‐Sr mineral isochron age of 177 ± 5 (2σ) Ma and an initial ⁸⁷Sr/⁸⁶Sr ratio (I_Sr) of 0.710364 ± 11 (2σ). Due to larger uncertainties of the Sm‐Nd isotopic data, no Sm‐Nd isochron age was obtained for GRV 99027. The ε¹⁴³Nd value is estimated approximately +12.2, assuming an age of 177 Ma. The I_Sr of GRV 99027 is distinguishable from other lherzolitic shergottites, confirming our previous conclusion that it is not paired with them ( Lin et al. 2005 ). The new data of GRV 99027 support the same age of approximately 180 Ma for most lherzolitic shergottites, and fill the small gap of I_Sr between Allan Hills A77005 and Lewis Cliff 88516 ( Borg et al. 2002 ). All available data are consistent with a single igneous source for the intermediate subgroup of lherzolitic shergottites.     

Martian meteorite Dhofar 019: A new shergottite

Abstract— Dhofar 019 is a new martian meteorite found in the desert of Oman. In texture, mineralogy, and major and trace element chemistry, this meteorite is classified as a basaltic shergottite. Olivine megacrysts are set within a groundmass composed of finer grained olivine, pyroxene (pigeonite and augite), and maskelynite. Minor phases are chromite‐ulvöspinel, ilmenite, silica, K‐rich feldspar, merrillite, chlorapatite, and pyrrhotite. Secondary phases of terrestrial origin include calcite, gypsum, celestite, Fe hydroxides, and smectite. Dhofar 019 is most similar to the Elephant Moraine (EETA) 79001 lithology A and Dar al Gani (DaG) 476/489 shergottites. The main features that distinguish Dhofar 019 from other shergottites are lack of orthopyroxene; lower Ni contents of olivine; the heaviest oxygen‐isotopic bulk composition; and larger compositional ranges for olivine, maskelynite, and spinel, as well as a wide range for pyroxenes. The large compositional ranges of the minerals are indicative of relatively rapid crystallization. Modeling of olivine chemical zonations yield minimum cooling rates of 0.5‐0.8 °C/h. Spinel chemistry suggests that crystallization took place under one of the most reduced conditions for martian meteorites, at an fO₂ 3 log units below the quartz‐fayalite‐magnetite (QFM) buffer. The olivine megacrysts are heterogeneously distributed in the rock. Crystal size distribution analysis suggests that they constitute a population formed under steady‐state conditions of nucleation and growth, although a few grains may be cumulates. The parent melt is thought to have been derived from partial melting of a light rare earth element‐ and platinum group element‐depleted mantle source. Shergottites, EETA79001 lithology A, DaG 476/489, and Dhofar 019, although of different ages, comprise a particular type of martian rocks. Such rocks could have formed from chemically similar source(s) and parent melt(s), with their bulk compositions affected by olivine accumulation.     

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.     

Melt inclusions in augite of the Nakhla martian meteorite: Evidence for basaltic parental melt

Abstract— Nakhla contains crystallized melt inclusions that were trapped in augite and olivine when these phases originally formed on Mars. Our study involved rehomogenization (slow‐heating and fast‐heating) experiments on multiphase melt inclusions in Nakhla augite. We studied melt inclusions trapped in augite because this phase re‐equilibrated with the external melt to a lesser extent than olivine and results could be directly compared with previous Nakhla melt inclusion studies. Following heating and homogenization of encapsulated melt inclusions, single mineral grains were mounted and polished to expose inclusions. Major element chemistry was determined by electron microprobe. The most primitive melt inclusion analyzed in Nakhla NA03 is basaltic and closely matches previously reported nakhlite parent melt compositions. MELTS equilibrium and fractional crystallization models calculated for NA03 and previous Nakhla parent melt estimates at QFM and QFM‐1 produced phase assemblages and compositions that can be compared to Nakhla. Of these models, equilibrium crystallization of NA03 at QFM‐1 produced the best match to mineral phases and compositions in Nakhla. In all models, olivine and augite co‐crystallize, consistent with the hypothesis that olivine is not xenocrystic but has undergone subsolidus re‐equilibration. In addition, measured melt inclusion compositions plot along the MELTS‐calculated liquid line of descent and may represent pockets of melt trapped at various stages during crystallization. We attempt to resolve discrepancies between previous estimates of the Nakhla parental melt composition and to reinterpret the results of a previous study of rehomogenized melt inclusions in Nakhla. Melt inclusions demonstrate that Nakhla is an igneous rock whose parent melt composition and crystallization history reflect planetary igneous processes.     

Petrography and mineralogy of the ungrouped type 3 carbonaceous chondrite Dar al Gani 978

Dar al Gani (DaG) 978 is an ungrouped type 3 carbonaceous chondrite. In this study, we report the petrography and mineralogy of Ca,Al‐rich inclusions (CAI), amoeboid olivine aggregates (AOAs), chondrules, mineral fragments, and the matrix in DaG 978. Twenty‐seven CAIs were found: 13 spinel‐diopside‐rich inclusions, 2 anorthite‐rich inclusions, 11 spinel‐troilite‐rich inclusions, and 1 spinel‐melilite‐rich inclusion. Most CAIs have a layered texture that indicates a condensation origin and are most similar to those in R chondrites. Compound chondrules represent a high proportion (approximately 8%) of chondrules in DaG 978, which indicates a local dusty chondrule‐forming region and multiple heating events. Most spinel and olivine in DaG 978 are highly Fe‐rich, which corresponds to a petrologic type of >3.5 and a maximum metamorphic temperature of approximately 850–950 K. This conclusion is also supported by other observations in DaG 978: the presence of coarse inclusions of silicate and phosphate in Fe‐Ni metal, restricted Ni‐Co distributions in kamacite and taenite, and low S concentrations in the matrix. Mineralogic records of iron‐alkali‐halogen metasomatism, such as platy and porous olivine, magnetite, hedenbergite, nepheline, Na‐rich in CAIs, and chlorapatite, are present, but relatively limited, in DaG 978. The fine‐grained, intergrowth texture of spinel‐troilite‐rich inclusions was probably formed by reaction between pre‐existing Al‐rich silicates and shock‐induced, high‐temperature S‐rich gas on the surface of the parent body of DaG 978. A shock‐induced vein is present in the matrix of DaG 978, which indicates that the parent body of DaG 978 at least experienced a shock event with a shock stage up to S3.     

Petrology of the Yamato nakhlites

Abstract— The Yamato nakhlites, Y‐000593, Y‐000749, and Y‐000802, were recovered in 2000 from the bare icefield around the Yamato mountains in Antarctica, consisting of three independent specimens with black fusion crusts. They are paired cumulate clinopyroxenites. We obtained the intercumulus melt composition of the Yamato nakhlites and here call it the Yamato intercumulus melt (YIM). The YIM crystallized to form the augite rims, the olivine rims and the mesostasis phases in the cumulates. The augite rims consist of two layers: inner and outer. The crystallization of the inner rim drove the interstitial melt into the plagioclase liquidus field. Subsequently, the residual melt crystallized pigeonites and plagioclase to form the outer rims and the mesostasis. Three types of inclusions were identified in olivine phenocrysts: rounded vitrophyric, angular vitrophyric, and monomineralic augite inclusions. The monomineralic augite inclusions are common and may have been captured by growing olivine phenocrysts. The rounded vitrophyric inclusions are rare and may represent the composition of middle‐stage melts, whereas the angular vitrophyric inclusions seem to have been derived from fractionated late‐stage melts. Glass inclusions occur in close association with titanomagnetite and ferroan augite halo in phenocryst core augites and the assemblages may be magmatic inclusions in augites. We compared the YIM with compositions of magmatic inclusions in olivine and augite. The composition of magmatic inclusions in augite is similar to the YIM. Phenocrystic olivines contain exsolution lamellae, augite‐magnetite aggregates, and symplectites in the cores. The symplectites often occur at the boundaries between olivine and augite grains. The aggregates, symplectite and lamellae formed by exsolution from the host olivine at magmatic temperatures. We present a formational scenario for nakhlites as follows: (1) accumulation of augite, olivine, and titanomagnetite phenocrysts took place on the floor of a magma chamber; (2) olivine exsolved augite and magnetite as augite‐magnetite aggregates, symplectites and lamellae; (3) the overgrowth on olivine phenocrysts formed their rims, and the inner rims crystallized on augite phenocryst cores; and finally, (4) the outer rim formed surrounding the inner rims of augite phenocrysts, and plagioclase and minor minerals crystallized to form mesostasis under a rapid cooling condition, probably in a lava flow or a sill.     

Expanding the application of the Eu‐oxybarometer to the lherzolitic shergottites and nakhlites: Implications for the oxidation state heterogeneity of the Martian interior

Abstract— Experimentally rehomogenized melt inclusions from the nakhlite Miller Range 03346 (MIL 03346) and the lherzolitic shergottite Allan Hills 77005 (ALH 77005) have been analyzed for their rare earth element (REE) concentrations in order to characterize the early melt compositions of these Martian meteorites and to calculate the oxygen fugacity conditions they crystallized under. D(Eu/Sm)_{pyroxene/melt} values were measured at 0.77 and 1.05 for ALH 77005 and MIL 03346, respectively. These melts and their associated whole rock compositions have similar REE patterns, suggesting that whole rock REE values are representative of those of the early melts and can be used as input into the pyroxene Eu‐oxybarometer for the nakhlites and lherzolitic shergottites. Crystallization fO₂ values of IW + 1.1 (ALH 77005) and IW + 3.2 (MIL 03346) were calculated. Whole rock data from other nakhlites and lherzolitic shergottites was input into the Eu‐oxybarometer to determine their crystallization fO₂ values. The lherzolitic shergottites and nakhlites have fO₂ values that range from IW + 0.4 to 1.6 and from IW + 1.1 to 3.2, respectively. These values are consistent with some previously determined fO₂ estimates and expand the known range of fO₂ values of the Martian interior to four orders of magnitude. The origins of this range are not well constrained. Possible mechanisms for producing this spread in fO₂ values include mineral/melt fractionation, assimilation, shock effects, and magma ocean crystallization processes. Mineral/melt partitioning can result in changes in fO₂ from the start to the finish of crystallization of 2 orders of magnitude. In addition, crystallization of a Martian magma ocean with reasonable initial water content results in oxidized, water‐rich, late‐stage cumulates. Sampling of these oxidized cumulates or interactions between reduced melts and the oxidized material can potentially account for the range of fO₂ values observed in the Martian meteorites.     

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.     

Glass‐bearing inclusions in olivine of the Chassigny achondrite: Heterogeneous trapping at sub‐igneous temperatures

Abstract— Three types of glass‐bearing inclusions are present in olivine and chromite of the Chassigny achondrite: pure glass, monocrystal (glass plus a single mineral grain), and multiphase (glass plus a variety of minerals) inclusions. The occurrence, texture, and mineralogy of these inclusions and the chemical composition of the glass suggest an origin by heterogeneous trapping of these phases. The glass is rich in SiO₂, Al₂O₃, Na₂O, K₂O; and poor in MgO, FeO, and CaO; and contains appreciable amounts of Cl. The compositional variability of the glass is independent of the mineral content of the inclusions. Heating experiments with final temperatures of 900, 1000, and 1200 °C were performed with Chassigny inclusions for the first time. The glass of the heated inclusions has a chemical composition similar to that of unheated inclusions. This situation suggests that the glass cannot be a residual melt but rather is an independent component that was trapped with or without mineral phases. The extreme heterogeneity in alkali contents, and in particular Rb and Sr contents, also suggests precipitation and mixing of solid precursors. The most Rb‐rich glasses have near‐chondritic Rb/Sr ratios, possibly indicating a chondritic source for their precursor(s). None of the inclusions contain bubbles like those of typical melt inclusions in terrestrial igneous minerals. Furthermore, many inclusions are at the center of radial cracks in the host olivine, which indicates development of an overpressure within the inclusions at some time. A volume increase of the inclusions could have been achieved by differential thermal expansion of the content of the inclusion during a heating event. That mechanism requires bubble‐free and solid preheating inclusion contents. These features are incompatible with an origin of the inclusions by trapping of a silicate melt and point toward heterogeneous trapping of solid phases. The first N analyses performed in Chassigny glass‐bearing inclusions by nuclear reaction analysis (NRA) revealed high and variable N contents of the glass, which suggests trapping of a solid precursor (presumably at relatively low temperatures) from a fluid rather than a melt. In conclusion, the glass‐bearing inclusions in Chassigny olivine are not residuals after a closed‐system evolution of a trapped melt, but rather heterogeneously trapped precipitates of a fluid that existed during formation of Chassigny constituents. Consequently, it is very unlikely that the host olivine has an igneous origin.     

Unique achondrite Northwest Africa 11042: Exploring the melting and breakup of the L chondrite parent body

Northwest Africa (NWA) 11042 is a heavily shocked achondrite with medium‐grained cumulate textures. Its olivine and pyroxene compositions, oxygen isotopic composition, and chromium isotopic composition are consistent with L chondrites. Sm‐Nd dating of its primary phases shows a crystallization age of 4100 ± 160 Ma. Ar‐Ar dating of its shocked mineral maskelynite reveals an age of 484.0 ± 1.5 Ma. This age coincides roughly with the breakup event of the L chondrite parent body evident in the shock ages of many L chondrites and the terrestrial record of fossil L chondritic chromite. NWA 11042 shows large depletions in siderophile elements (<0.01×CI) suggestive of a complex igneous history involving extraction of a Fe‐Ni‐S liquid on the L chondrite parent body. Due to its relatively young crystallization age, the heat source for such an igneous process is most likely impact. Because its mineralogy, petrology, and O isotopes are similar to the ungrouped achondrite NWA 4284 (this work), the two meteorites are likely paired and derived from the same parent body.     

Shock‐induced melting,recrystallization, and exsolution in plagioclase from the Martian lherzolitic shergottite GRV 99027

Abstract— Plagioclase in the Martian lherzolitic shergottite Grove Mountains (GRV) 99027 was shocked, melted, and recrystallized. The recrystallized plagioclase contains lamellae of pyroxene, olivine, and minor ilmenite (<1 μm wide). Both the pyroxene and the olivine inclusions enclosed in plagioclase and grains neighboring the plagioclase were partially melted into plagioclase melt pools. The formation of these lamellar inclusions in plagioclase is attributed to exsolution from recrystallizing melt. Distinct from other Martian meteorites, GRV 99027 contains no maskelynite but does contain recrystallized plagioclase. This shows that the meteorite experienced a slower cooling than maskelynite‐bearing meteorites. We suggest that the parent rock of GRV 99027 could have been embedded in hot rocks, which facilitated a more protracted cooling history.     

Sayh al Uhaymir 094: A new martian meteorite from the Oman desert

Abstract— Sayhal Uhaymir (SaU) 094 is a 223.3 g, partially crusted, strongly to very strongly shocked melanocratic olivine-porphyric rock of the shergottite group showing a microgabbroic texture. The rock consists of pyroxene (52.0–58.2 vol%)—dominantly prismatic pigeonite (En_60–68Fs_20–27Wo^7–9) associated with minor augite (En_46–49Fs_15–16Wo_28–31)—brown (shock-oxidized) olivine (Fo_65–69; 22.1–31%), completely isotropic interstitial plagioclase glass (maskelynite; An_50–64Or_0.3-0.9; 8.6–13.0%), chromite and titanian magnesian chromite (0.9-1.0%), traces of ilmenite (Ilm_80–86), pyrrhotite (Fe_92–100; 0.1-0.2%), merrillite (<<0.1%), and pockets (4.8-6.7%) consisting of green basaltic to basaltic andesitic shock glass that is partially devitrified into a brown to black product along boundaries with the primary minerals. The average maximum dimensions of minerals are: olivine (1.5 mm), pyroxene (0.3 mm) and maskelynite (0.3 mm). Primary melt inclusions in olivine and chromite are common and account for 0.1-0.6% of the rock. X-ray tomography revealed that the specimen contains ˜0.4 vol% of shock-melt associated vesicles, up to 3 mm in size, which show a preferred orientation. Fluidization of the maskelynite, melting and recrystallization of pyroxene, olivine and pyrrhotite indicate shock stage S6. Minor terrestrial weathering resulted in calcite-veining and minor oxidation of sulfides. The meteorite is interpreted as paired with SaU 005/008/051. The modal composition is similar to Dar al Gani 476/489/670/735/876, with the exception that neither mesostasis nor titanomagnetite nor apatite are present and that all phases show little zonation. The restricted mineral composition, predominance of chromite among the oxides, and abundance of olivine indicate affinities to the lherzolitic shergottites.     

Ion microprobe U‐Th‐Pb dating of phosphates in martian meteorite ALH 84001

Abstract— Phosphates in martian meteorites are important carriers of trace elements, although, they are volumetrically minor minerals. PO₄ also has potential as a biomarker for life on Mars. Here, we report measurements of the U‐Th‐Pb systematics of phosphates in the martian meteorite ALH 84001 using the Sensitive High Resolution Ion MicroProbe (SHRIMP) installed at Hiroshima University, Japan. Eleven analyses of whitlockites and 1 analysis of apatite resulted in a total Pb/U isochron age of 4018 ± 81 Ma in the ²³⁸U/²⁰⁶Pb‐²⁰⁷Pb/²⁰⁶Pb‐²⁰⁴Pb/²⁰⁶ Pb 3‐D space, and a ²³²Th‐²⁰⁸Pb age of 3971 ± 860 Ma. These ages are consistent within a 95% confidence limit. This result is in agreement with the previously published Ar‐Ar shock age of 4.0 ± 0.1 Ga from maskelynite and other results of 3.8–4.3 Ga but are significantly different from the Sm‐Nd age of 4.50 ± 0.13 Ga based on the whole rock and pyroxene. Taking into account recent studies on textural and chemical evidence of phosphate, our result suggests that the shock metamorphic event defines the phosphate formation age of 4018 ± 81 Ma, and that since then, ALH 84001 has not experienced a long duration thermal metamorphism, which would reset the U‐Pb system in phosphates.     

Petrology and geochemistry of olivine‐phyric shergottites LAR 12095 and LAR 12240: Implications for their petrogenetic history on Mars

Larkman Nunatak (LAR) 12095 and LAR 12240 are recent olivine‐phyric shergottite finds. We report the results of petrographic and chemical analyses of these two samples to understand their petrogenesis on Mars. Based on our analyses, we suggest that these samples are likely paired and are most similar to other depleted olivine‐phyric shergottites, particularly Dar al Gani (DaG) 476 and Sayh al Uhaymir (SaU) 005 (and samples paired with those). The olivine megacryst cores in LAR 12095 and LAR 12240 are not in equilibrium with the groundmass olivines. We infer that these megacrysts are phenocrysts and their major element compositions have been homogenized by diffusion (the cores of the olivine megacrysts have Mg# ~70, whereas megacryst rims and groundmass olivines typically have Mg# ~58–60). The rare earth element (REE) microdistributions in the various phases (olivine, low‐ and high‐Ca pyroxene, maskelynite, and merrillite) in both samples are similar and support the likelihood that these two shergottites are indeed paired. The calculated parent melt (i.e., in equilibrium with the low‐Ca pyroxene, which is one of the earliest formed REE‐bearing minerals) has an REE pattern parallel to that of melt in equilibrium with merrillite (i.e., one of the last‐formed minerals). This suggests that the LAR 12095/12240 paired shergottites represent the product of closed‐system fractional crystallization following magma emplacement and crystal accumulation. Utilizing the europium oxybarometer, we estimate that the magmatic oxygen fugacity early in the crystallization sequence was ~IW. Finally, petrographic evidence indicates that LAR 12095/12240 experienced extensive shock prior to being ejected from Mars.