Crystallization of the basaltic shergottites: Insights from crystal size distribution (CSD) analysis of pyroxenes

Abstract— Quantitative petrographic analysis, using the crystal size distribution (CSD) method, provides a novel approach for examining the crystallization histories of basaltic shergottites. Grain number densities at different sizes are plotted against grain size, and the resulting curve relates to the geologic processes involved with the crystallization of the grain population. Most basaltic shergottites are dominated by pigeonite and augite; and because plagioclase is primarily interstitial, and therefore constrained in its growth by the surrounding pyroxenes, we limited our size measurements to the pyroxene phases. The groundmasses of Elephant Moraine (EET) A79001 lithology A and Dar al Gani (DaG) 476 are fine grained with cumulus pyroxene and interstitial plagioclase glass. Their simple linear CSD plots record a single stage of pyroxene crystallization under steady‐state conditions of continuous nucleation and growth. The textures of Queen Alexandra Range (QUE) 94201 and EETA79001 lithology B are quite different from the other shergottites, with intergrown pyroxene and plagioclase. Likewise, their CSD plots are also distinct, with curved trends that suggest a lack of large grains, most likely because of interference between simultaneously growing silicate phases. However, the CSD plot shapes are smooth, also implying a single stage of growth. Shergotty and Zagami, with coarser cumulus textures, display CSD plots that are generally linear over most grain sizes. This implies that conditions of nucleation and growth were dominant during formation of the pyroxene populations. Both plots, however, also display kinks, implying multiple stages of growth. A similar kink is also visible in a CSD plot of only the Mg‐rich cores of Shergotty pyroxenes, which suggests the feature represents changes in conditions during core crystallization, rather than an event coincident with the change in composition to the Fe‐rich rims. The plot may be interpreted as representing two stages of core growth with an intervening short hiatus of nucleation, with continued crystallization associated with ascent of the magma. Eruption onto the surface probably triggered the compositional change to Fe‐rich rims. The CSD analysis of products from a controlled crystallization study agree with experimental and petrologic estimates that cooling rates for Zagami were on the order of a few tenths of a degree per hour. Growth rates derived from these cooling rates suggest crystallization of Shergotty and Zagami pyroxenes occurred over a period of a few weeks to months.     

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.     

Mineralogy and petrology of the Dar al Gani 476 martian meteorite: Implications for its cooling history and relationship to other shergottites

Abstract— Dar al Gani 476, the 13th martian meteorite, was recovered from the Sahara in 1998. It is a basaltic shergottitic rock composed of olivine megacrysts reaching 5 mm (24 vol%) set in a finegrained groundmass of pyroxene (59 vol%) and maskelynitized plagioclase (12 vol%) with minor amounts of accessory phases (spinel, merrillite, ilmenite). Dar al Gani 476 is similar to lithology A of Elephant Moraine A79001 (EETA79001) in petrography and mineralogy, but is distinct in several aspects. Low‐Ca pyroxenes in the Dar al Gani 476 groundmass are more magnesian (En₇₆Fs₂₁ Wo₃～En₅₈Fs₃₀Wo₁₂) than those in lithology A of EETA79001 (En₇₃Fs₂₂Wo₅～En₄₅Fs₄₃Wo₁₂), rather similar to pyroxenes in lherzolitic martian meteorites (En₇₆Fs₂₁ Wo₃～En₆₃Fs₂₂Wo₁₅). Dar al Gani 476 olivine is less magnesian and shows a narrower compositional range (Fo_76‐58) than EETA79001 olivine (Fo_81‐53), and is also similar to olivines in lherzolitic martian meteorites (Fo_74‐65). The orthopyroxene‐olivine‐chromite xenolith typical in the lithology A of EETA79001 is absent in Dar al Gani 476. It seems that Dar al Gani 476 crystallized from a slightly more primitive mafic magma than lithology A of EETA79001 and several phases (olivine, pyroxene, chromite, and ilmenite) in Dar al Gani 476 may have petrogenetic similarities to those of lherzolitic martian meteorites. Olivine megacrysts in Dar al Gani 476 are in disequilibrium with the bulk composition. The presence of fractured olivine grains in which the most Mg‐rich parts are in contact with the groundmass suggests that little diffusive modification of original olivine compositions occurred during cooling. This observation enabled us to estimate the cooling rates of Dar al Gani 476 and EETA79001 olivines, giving similar cooling rates of 0.03‐3 °C/h for Dar al Gani 476 and 0.05‐5 °C/h for EETA79001. This suggests that they were cooled near the surface (burial depth shallower than about 3 m at most), probably in lava flows during crystallization of groundmass. As is proposed for lithology A of EETA79001, it may be possible to consider that Dar al Gani 476 has an impact melt origin, a mixture of martian lherzolite and other martian rock (Queen Alexandra Range 94201, nakhlites?).     

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.     

Petrology and chemistry of the new shergottite Dar al Gani 476

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

Petrology and 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.     

Mineral chemistry of the Tissint meteorite: Indications of two‐stage crystallization in a closed system

The Tissint meteorite is a geochemically depleted, olivine‐phyric shergottite. Olivine megacrysts contain 300–600 μm cores with uniform Mg# (~80 ± 1) followed by concentric zones of Fe‐enrichment toward the rims. We applied a number of tests to distinguish the relationship of these megacrysts to the host rock. Major and trace element compositions of the Mg‐rich core in olivine are in equilibrium with the bulk rock, within uncertainty, and rare earth element abundances of melt inclusions in Mg‐rich olivines reported in the literature are similar to those of the bulk rock. Moreover, the P Kα intensity maps of two large olivine grains show no resorption between the uniform core and the rim. Taken together, these lines of evidence suggest the olivine megacrysts are phenocrysts. Among depleted olivine‐phyric shergottites, Tissint is the first one that acts mostly as a closed system with olivine megacrysts being the phenocrysts. The texture and mineral chemistry of Tissint indicate a crystallization sequence of: olivine (Mg# 80 ± 1) → olivine (Mg# 76) + chromite → olivine (Mg# 74) + Ti‐chromite → olivine (Mg# 74–63) + pyroxene (Mg# 76–65) + Cr‐ulvöspinel → olivine (Mg# 63–35) + pyroxene (Mg# 65–60) + plagioclase, followed by late‐stage ilmenite and phosphate. The crystallization of the Tissint meteorite likely occurred in two stages: uniform olivine cores likely crystallized under equilibrium conditions; and a fractional crystallization sequence that formed the rest of the rock. The two‐stage crystallization without crystal settling is simulated using MELTS and the Tissint bulk composition, and can broadly reproduce the crystallization sequence and mineral chemistry measured in the Tissint samples. The transition between equilibrium and fractional crystallization is associated with a dramatic increase in cooling rate and might have been driven by an acceleration in the ascent rate or by encounter with a steep thermal gradient in the Martian crust.     

A new martian meteorite from the Sahara: The shergottite Dar al Gani 489

Abstract— Dar al Gani 489 (DaG 489) is a meteorite fragment of 2146 g found in the Libyan Sahara by a meteorite finder during one of his search campaigns in 1997–98. It is a porphyritic rock with millimetersized olivine crystals (Fo_79–59) set in a fine‐grained groundmass (average grain size 0.1 mm) consisting of pigeonite (En_75–57 Wo_5–15) crystals and interstitial feldspathic glass (An_67–56 Or_0–1). Minor phases include enstatite (En_82–71 Wo_2–4), augite (En_48–52 Wo_29–32), chromite, Ti‐chromite, ilmenite, pyrrhotite, merrillite, and secondary calcite and iron oxides. On the basis of mineralogical, petrographic, bulk chemical, O‐isotopic, and noble gas data, DaG 489 can be classified as a highly shocked martian meteorite (e.g., Fe/Mn_(bulk) = 42.1, Ni/Mg_(bulk) = 0.002; δ¹⁷O = 2.89, δ¹⁸O = 4.98, and Δ¹⁷O = 0.305), belonging to the basaltic shergottite subgroup. The texture and modal composition of DaG 489 are indeed those of basalts; nonetheless, the bulk chemistry, the abundance of large olivine and chromite crystals, and enstatitic pyroxene suggest some relationship with lherzolitic shergottites. As such, DaG 489 is similar to the hybrid shergottite Elephant Moraine (EET) A79001 lithology A; however, there are some relevant differences including a higher olivine content (20 vol%), the lack of orthopyroxene megacrysts, a higher molar Mg/(Mg + Fe)_(molar) = 0.68, and a lower rare earth element content in the bulk sample. Therefore, DaG 489 has the potential of providing us with a further petrogenetic link between the basaltic and lherzolitic shergottites. Noble gases data show that DaG 489 has an ejection age of ～1.3 Ma. This young age lends support to the requirement of several ejection events to produce the current population of shergottites, nakhlites, and chassignites (SNC) meteorites. In terms of texture, mineral and bulk compositions, shock level, and weathering features, DaG 489 is essentially identical to DaG 476, another basaltic shergottite independently found ～25 km due northnortheast of DaG 489. Because DaG 489 also has the same exposure history as DaG 476, it is very likely that both meteorites are fragments of the same fall. In addition to the existing hypotheses on the petrogenesis of the similar EETA79001 lithology A and the identical DaG 476, we propose that DaG 489 could have formed through high‐degree partial melting of a lherzolite‐like material.     

Petrogenetic linkages among Martian basalts: Implications based on trace element chemistry of olivine

Abstract— The shergottites exhibit a range of major and trace element compositions, crystallization ages, and initial Sr, Nd, Hf, and Pb isotopic compositions. To constrain the physical mechanisms by which shergottites obtain their compositional characteristics, we examined the major and trace element record preserved in olivine in the more primitive shergottites. Based on such characteristics as the Mg#, V zoning, calculated D_Ni,Co, the olivine in Y‐980459 are most likely phenocrysts. Many of these same characteristics indicate that the olivines in other shergottites are not in equilibrium with the adjacent melt. However, in most cases they are not xenocrystic, but additions of olivine from the same basaltic system. Elephant Moraine (EET) A79001 may be an exception with the olivine data suggesting that it is xenocrystic. In this case, the olivine crystallized from a reduced and LREE‐depleted melt and was incorporated into an oxidized and enriched basalt. Vanadium and CaO in olivine appear to record the appearance of spinel and pyroxene on the liquidus of most of the shergottites. Most of the olivine shergottites represent basalts produced by melting of reduced (IW to IW + 1), depleted mantle sources. Olivine data indicate that many of the primary melts derived from this source had similar Ni, Co, and Mn. Shergottites such as Northwest Africa (NWA) 1110/1068 and perhaps Roberts Massif (RBT) 04261 that appear to be derived from more enriched sources have distinctly different olivine. In the case of NWA 1110/1068, the olivine data suggests that the enriched component was added to system prior to olivine crystallization.     

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.     

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.     

Hydrous olivine alteration on Mars and Earth

Hydrous alteration of olivine macrocrysts in a Martian olivine phyric basalt, NWA 10416, and a terrestrial basalt from southern Colorado are examined using SEM, EPMA, TEM, and µXRD techniques. The olivines in the meteorite contain linear nanotubes of hydrous material, amorphous areas, and fluid dissolution textures quite distinct from alteration identified in other Martian meteorites. Instead, they bear resemblance to terrestrial deuteric alteration features. The presence of the hydrous alteration phase Mg‐laihunite within the olivines has been confirmed by µXRD analysis. The cores of the olivines in both Martian and terrestrial samples are overgrown by unaltered rims whose compositions match those of a separate population of groundmass olivines, suggesting that the core olivines are xenocrysts whose alteration preceded crystallization of the groundmass. The terrestrial sample is linked to deep crustal metasomatism and the “ignimbrite flare‐up” of the Oligocene epoch. The comparison of the two samples suggests the existence of an analogous relatively water‐rich magmatic reservoir on Mars.     

Caleta el Cobre 022 Martian meteorite: Increasing nakhlite diversity

Caleta el Cobre (CeC) 022 is a Martian meteorite of the nakhlite group, showing an unbrecciated cumulate texture, composed mainly of clinopyroxene and olivine. Augite shows irregular core zoning, euhedral rims, and thin overgrowths enriched in Fe relative to the core. Low‐Ca pyroxene is found adjacent to olivine. Phenocrysts of Fe‐Ti oxides are titanomagnetite with exsolutions of ilmenite/ulvöspinel. Intercumulus material consists of both coarse plagioclase and fine‐grained mesostasis, comprising K‐feldspars, pyroxene, apatite, ilmenite, Fe‐Ti oxides, and silica. CeC 022 shows a high proportion of Martian aqueous alteration products (iddingsite) in olivine (45.1 vol% of olivine) and mesostasis. This meteorite is the youngest nakhlite with a distinct Sm/Nd crystallization age of 1.215 ± 0.067 Ga. Its ejection age of 11.8 ± 1.8 Ma is similar to other nakhlites. CeC 022 reveals contrasted cooling rates with similarities with faster cooled nakhlites, such as Northwest Africa (NWA) 817, NWA 5790, or Miller Range 03346 nakhlites: augite irregular cores, Fe‐rich overgrowths, fine‐grained K‐feldspars, quenched oxides, and high rare earth element content. CeC 022 also shares similarities with slower cooled nakhlites, including Nakhla and NWA 10153: pyroxene modal abundance, pyroxenes crystal size distribution, average pyroxene size, phenocryst mineral compositions, unzoned olivine, and abundant coarse plagioclase. Moreover, CeC 022 is the most magnetic nakhlite and represents an analog source lithology for the strong magnetization of the Martian crust. With its particular features, CeC 022 must originate from a previously unsampled sill or flow in the same volcanic system as the other nakhlites, increasing Martian sample diversity and our knowledge of nakhlites.     

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.     

KREEPy lunar meteorite Dhofar 287A: A new lunar mare basalt

Abstract— Dhofar 287 (Dho 287) is a new lunar meteorite, found in Oman on January 14, 2001. The main portion of this meteorite (Dho 287A) consists of a mare basalt, while a smaller portion of breccia (Dho 287B) is attached on the side. Dho 287A is only the fourth crystalline mare basalt meteorite found on Earth to date and is the subject of the present study. The basalt consists mainly of phenocrysts of olivine and pyroxene set in a finer‐grained matrix, which is composed of elongated pyroxene and plagioclase crystals radiating from a common nucleii. The majority of olivine and pyroxene grains are zoned, from core to rim, in terms of Fe and Mg. Accessory minerals include ilmenite, chromite, ulvöspinel, troilite, and FeNi metal. Chromite is invariably mantled by ulvöspinel. This rock is unusually rich in late‐stage mesostasis, composed largely of fayalite, Si‐K‐Ba‐rich glass, fluorapatite, and whitlockite. In texture and mineralogy, Dho 287A is a low‐Ti mare basalt, with similarities to Apollo 12 (A‐12) and Apollo 15 (A‐15) basalts. However, all plagioclase is now present as maskelynite, and its composition is atypical for known low‐Ti mare basalts. The Fe to Mn ratios of olivine and pyroxene, the presence of FeNi metal, and the bulk‐rock oxygen isotopic ratios, along with several other petrological features, are evidence for the lunar origin for this meteorite. Whole‐rock composition further confirms the similarity of Dho 287A with A‐12 and A‐15 samples but requires possible KREEP assimilation to account for its rare‐earth‐element (REE) contents. Cooling‐rate estimates, based on Fo zonation in olivine, yield values of 0.2–0.8°C/hr for the lava, typical for the center of a 10–20 m thick flow. The recalculated major‐element concentrations, after removing 10–15% modal olivine, are comparable to typical A‐15 mare basalts. Crystallization modeling of the recalculated Dho 287A bulk‐composition yields a reasonable fit between predicted and observed mineral abundances and compositions.     

Trace elements in olivine and the petrogenesis of the intermediate,olivine‐phyric shergottite NWA 10170

Olivine‐phyric shergottites represent primitive basaltic to picritic rocks, spanning a large range of Mg# and olivine abundances. As primitive olivine‐bearing magmas are commonly representative of their mantle source on Earth, understanding the petrology and evolution of olivine‐phyric shergottites is critical in our understanding of Martian mantle compositions. We present data for the olivine‐phyric shergottite Northwest Africa (NWA) 10170 to constrain the petrology with specific implications for magma plumbing‐system dynamics. The calculated oxygen fugacity and bulk‐rock REE concentrations (based on modal abundance) are consistent with a geochemically intermediate classification for NWA 10170, and overall similarity with NWA 6234. In addition, we present trace element data using laser ablation ICP‐MS for coarse‐grained olivine cores, and compare these data with terrestrial and Martian data sets. The olivines in NWA 10170 contain cores with compositions of Fo₇₇ that evolve to rims with composition of Fo₅₈, and are characterized by cores with low Ni contents (400–600 ppm). Nickel is compatible in olivine and such low Ni content for olivine cores in NWA 10170 suggests either early‐stage fractionation and loss of olivine from the magma in a staging chamber at depth, or that Martian magmas have lower Ni than terrestrial magmas. We suggest that both are true in this case. Therefore, the magma does not represent a primary mantle melt, but rather has undergone 10–15% fractionation in a staging chamber prior to extrusion/intrusion at the surface of Mars. This further implies that careful evaluation of not only the Mg# but also the trace element concentrations of olivine needs to be conducted to evaluate pristine mantle melts versus those that have fractionated olivine (±pyroxene and oxide minerals) in staging chambers.     

Defining the mechanisms that disturb the Sm‐Nd isotopic systematics of the Martian meteorites: Examples from Dar al Gani 476 and Allan Hills 77005

Abstract— Microbeam studies of Martian meteorites Dar al Gani (DaG) 476 and Allan Hills (ALH) 77005 have been conducted to identify potential causes of disequilibrium exhibited in their Sm‐Nd isotopic systematics. Olivine and maskelynite mineral fractions on the DaG 476 isochron are displaced relative to their positions as dictated by measured mineral compositions. The olivine mineral fractions from ALH 77005 not only have a relatively low Sm/Nd ratio, but appear to contain an unradiogenic component that shifts the olivine mineral fraction off the isochron defined by the pyroxene and maskelynite mineral fractions. Trace components such as melt inclusions, impact melt, high‐Si mesostasis, and altered olivine were analyzed using scanning electron microscopy, quantitative electron microscopy, and secondary ion mass spectrometry to determine their potential for disturbing the isotopic systematics of the mineral fractions, assuming that the mineral fractions were not completely pure. Mixing models indicate that the presence of melt inclusions in the DaG 476 olivine mineral fraction lowered its Sm/Nd ratio. The maskelynite mineral fraction contains a related but more evolved mesostasis component that raised the Sm/Nd ratio of the fraction. The position of two olivine mineral fractions below the ALH 77005 isochron is interpreted to reflect small additions of impact melt with a light rare earth element enriched pattern and a non‐indigenous, unradiogenic Nd component. Furthermore, the presence of rare earth elements in olivine and maskelynite from both igneous and non‐igneous components such as melt inclusions, mesostasis, and impact melt is observed on a fine (<30 μm) scale. Despite the addition of this material, the Sm‐Nd ages are not affected. This study demonstrates that detailed mineral separation procedures as employed by modern geochronology laboratories permit reliable ages to be derived from shocked and altered samples.     

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.     

Lithium isotopes and light lithophile element abundances in shergottites: Evidence for both magmatic degassing and subsolidus diffusion

Degassed magmatic water was potentially the major source of surficial water on Mars. We measured Li, B, and Be abundances and Li isotope profiles in pyroxenes, olivines, and maskelynite from four compositionally different shergottites—Shergotty, QUE 94201, LAR 06319, and Tissint—using secondary ion mass spectrometry (SIMS). All three light lithophile elements (LLE) are incompatible: Li and B are soluble in H₂O‐rich fluids, whereas Be is insoluble. In the analyzed shergottites, Li concentration decreases and Be concentration increases from cores to rims in pyroxenes. However, B concentrations do not vary consistently with Li and Be abundances, except in QUE 94201 pyroxenes. Additionally, abundances of these three elements in olivines show a normal igneous‐fractionation trend consistent with the crystallization of olivine before magma ascent and degassing. We expect that kinetic effects would lead to fractionation of ⁶Li in the vapor phase compared to ⁷Li during degassing. The Li isotope profiles, with increasing δ⁷Li from cores to rims, as well as Li and B profiles indicate possible degassing of hydrous fluids only for the depleted shergottite QUE 94201, as also supported by degassing models. Conversely, Shergotty, LAR 06319, and Tissint appear to have been affected by postcrystallization diffusion, based on their LLE and Li isotope profiles, accompanied by diffusion models. This process may represent an overlay on a degassing pattern. The LLE profiles and isotope profiles in QUE 94201 support the hypothesis that degassing of some basaltic shergottite magmas provided water to the Martian surface, although evidence may be obscured by subsolidus diffusion processes.     

Petrogenesis of lunar highlands meteorites: Dhofar 025, Dhofar 081, Dar al Gani 262, and Dar al Gani 400

Abstract— The petrogenesis of four lunar highlands meteorites, Dhofar 025 (Dho 025), Dhofar 081 (Dho 081), Dar al Gani 262 (DaG 262), and Dar al Gani 400 (DaG 400) were studied. For Dho 025, measured oxygen isotopic values and Fe‐Mn ratios for mafic minerals provide corroboratory evidence that it originated on the Moon. Similarly, Fe‐Mn ratios in the mafic minerals of Dho 081 indicate lunar origin. Lithologies in Dho 025 and Dho 081 include lithic clasts, granulites, and mineral fragments. A large number of lithic clasts have plagioclase AN# and coexisting mafic mineral Mg# that plot within the “gap” separating ferroan anorthosite suite (FAN) and high‐magnesium suite (HMS) rocks. This is consistent with whole rock Ti‐Sm ratios for Dho 025, Dho 081, and DaG 262, which are also intermediate compared to FAN and HMS lithologies. Although ion microprobe analyses performed on Dho 025, Dho 081, DaG 262, and DaG 400 clasts and minerals show far stronger FAN affinities than whole rock data suggest, most clasts indicate admixture of ≤12% HMS component based on geochemical modeling. In addition, coexisting plagioclase‐pyroxene REE concentration ratios in several clasts were compared to experimentally determined plagioclase‐pyroxene REE distribution coefficient ratios. Two Dho 025 clasts have concordant plagioclase‐pyroxene profiles, indicating that equilibrium between these minerals has been sustained despite shock metamorphism. One clast has an intermediate FAN‐HMS composition. These lunar meteorites appear to represent a type of highland terrain that differs substantially from the KREEP‐signatured impact breccias that dominate the lunar database. From remote sensing data, it is inferred that the lunar far side appears to have appropriate geochemical signatures and lithologies to be the source regions for these rocks; although, the near side cannot be completely excluded as a possibility. If these rocks are, indeed, from the far side, their geochemical characteristics may have far‐reaching implications for our current scientific understanding of the Moon.