Basaltic magmatism and the bulk composition of the moon

The lunar interior is comprised of two major petrological provinces: (1) an outer zone several hundred km thick which experienced partial melting and crystallization differentiation 4.4–4.6 b.y. ago to form the lunar crust together with an underlying complementary zone of ultramafic cumulates and residua, and (2) the primordial deep interior which was the source region for mare basalts (3.2–3.8 b.y.) and had previously been contaminated to varying degrees with highly fractionated material derived from the 4.4–4.6 b.y. differentiation event. In both major petrologic provinces, basaltic magmas have been produced by partial melting. The chemical characteristics and high-pressure phase relationships of these magmas can be used to constrain the bulk compositions of their respective source regions.Primitive low-Ti mare basalts (e.g., 12009, 12002, 15555 and Green Glass) possessing high normative olivine and high Mg and Cr contents, provide the most direct evidence upon the composition of the primordial deep lunar interior. This composition, as estimated on the basis of high pressure equilibria displayed by the above basalts, combined with other geochemical criteria, is found to consist of orthopyroxene + clinopyroxene + olivine with total pyroxenes > olivine, 100 MgO/(MgO + FeO) = 75–80, about 4% of CaO and Al₂O₃ and 2× chondritic abundances of REE, U and Th. This composition is similar to that of the earth's mantle except for a higher pyroxene/olivine ratio and lower 100 MgO/(MgO + FeO).The lunar crust is believed to have formed by plagioclase elutriation within a vast ocean of parental basaltic magma. The composition of the latter is found experimentally by removing liquidus plagioclase from the observed mean upper crust (gabbroic anorthosite) composition, until the resulting composition becomes multiply saturated with plagioclase and a ferromagnesian phase (olivine). This parental basaltic composition is almost identical with terrestrial oceanic tholeiites, except for partial depletion in the two most volatile components, Na₂ and SiO₂. Similarity between these two most abundant classes of lunar and terrestrial basaltic magmas strongly implies corresponding similarities between their source regions. The bulk composition of the outer 400 km of the Moon as constrained by the 4.6-4.4 b.y. parental basaltic magma is found to be peridotitic, with olivine > pyroxene, 100 MgO/ (MgO + FeO) 86, and about 2× chondritic abundances of Ca, Al and REE. The Moon thus appears to have a zoned structure, with the deep interior (below 400 km) possessing somewhat higher contents of FeO and SiO₂ than the outer 400 km. This zoned model, derived exclusively on petrological grounds, provides a quantitative explanation of the Moon's mean density, moment of inertia and seismic velocity profile.The bulk composition of the entire Moon, thus obtained, is very similar to the pyrolite model composition for the Earth's mantle, except that the Moon is depleted in Na (and other volatile elements) and somewhat enriched in iron. The similarity in major element composition extends also to the abundances of REE, U and Th. These compositional similarities, combined with the identity in oxygen isotope ratios between the Moon and the Earth's mantle, are strongly suggestive of a common genetic relationship.     

The water content and parental magma of the second chassignite NWA 2737: Clues from trapped melt inclusions in olivine

NWA 2737, the second known chassignite, mainly consists of cumulate olivine crystals of homogeneous composition (Fo = 78.7 ± 0.9). These brown colored olivine grains exhibit two sets of perpendicular planar defects due to shock. Two forms of trapped liquids, interstitial melts and magmatic inclusions, have been examined. Mineral assemblages within the olivine‐hosted magmatic inclusions include low‐Ca pyroxene, augite, kaersutite, fluorapatite, biotite, chromite, sulfide, and feldspathic glass. The reconstructed parental magma composition (A^#) of the NWA 2737 is basaltic and resembles both the experimentally constrained parental melt composition of chassiginites and the Gusev basalt Humphrey, albeit with lower Al contents. A^# also broadly resembles the average of shergottite parent magmas or LAR 06319. However, we suggest that the mantle source for the chassignite parental magmas was distinct from that of the shergottite meteorites, particularly in CaO/Al₂O₃ ratio. In addition, based on the analysis of the volatile contents of kaersutite, we derived a water content of 0.48–0.67 wt% for the parental melt. Finally, our MELTS calculations suggest that moderate pressure (approximately 6.8 kb) came closest to reproducing the crystallized melt‐inclusion assemblages.     

Mineralogical composition of (25143) Itokawa 1998 SF36 from visible and near‐infrared reflectance spectroscopy: Evidence for partial melting

Abstract— –In March 2001, asteroid (25143) Itokawa, the target of the Japanese Hayabusa spacecraft mission, was in a favorable viewing geometry for ground‐based telescopic study. Visible/near‐infrared (VNIR) spectra (～～0.48 to 0.9 μm) obtained on March 24, 26, and 27 UT, and near‐infrared (NIR) spectra (～～0.75 to 2.5 μm) obtained on March 10, 11, 12, 23, and 24 UT collectively show absorption features centered near 1.0 and 2.0 μm, which are indicative of olivine and pyroxene. Analyses of these absorption features indicate an abundance ratio of olivine to pyroxene of approximately 75:25 ± 5, respectively, with no significant variation in the relative abundance of these minerals across its surface on a regional scale. The band center positions indicate that the mean pyroxene chemistry is ～～Wo_{14 ± 5}Fs_{43 ± 5}. There appear to be at least two pyroxene components: primarily a low‐Ca orthopyroxene accompanied by a spectrally significant (～～15–20%) high Fe‐rich pigeonite phase. The mean pyroxene composition is significantly more Fe‐rich than the Fs_14–26 range found in ordinary chondrites. These pyroxene compositions are suggestive of phases crystallized from partial melts. This would indicate that the parent body of (25143) Itokawa reached temperatures sufficient to initiate partial melting (～～1050 to 1250 °C), but that it did not attain the degree of melting required for significant melt mobilization and efficient segregation of the basaltic melt component from the unmelted residual olivine portion. Itokawa's spectral band parameters place it near the S(III)/S(IV) boundary, but within the S(III) taxonomic field. In meteoritic nomenclature, Itokawa would be most analogous to an olivine‐rich primitive achondrite. Alternatively, if the high Fs value is not related to partial melting, then Itokawa could also represent a rare atypical LL chondrite, or a previously unsampled oxidized Fe‐rich chondritic‐like assemblage.     

Northwest Africa 032: Product of lunar volcanism

Abstract— Mineralogy, major element compositions of minerals, and elemental and oxygen isotopic compositions of the whole rock attest to a lunar origin of the meteorite Northwest Africa (NWA) 032, an unbrecciated basalt found in October 1999. The rock consists predominantly of olivine, pyroxene and chromite phenocrysts, set in a crystalline groundmass of feldspar, pyroxene, ilmenite, troilite and trace metal. Whole‐rock shock veins comprise a minor, but ubiquitous portion of the rock. Undulatory to mosaic extinction in olivine and pyroxene phenocrysts and micro‐faults in groundmass and phenocrysts also are attributed to shock. Several geochemical signatures taken together indicate unambiguously that NWA 032 originated from the Moon. The most diagnostic criteria include whole‐rock oxygen isotopic composition and ratios of Fe/Mn in the whole rock, olivine, and pyroxene. A lunar origin is documented further by the presence of Fe‐metal, troilite, and ilmenite; zoning to extremely Fe‐rich compositions in pyroxene; the ferrous oxidation state of all Fe in pyroxene; and the rare earth element (REE) pattern with a well‐defined negative europium anomaly. This rock is similar in major element chemistry to basalts from Apollo 12 and 15, but is enriched in light REE and has an unusually high Th/Sm ratio. Some Apollo 14 basalts yield a closer match to NWA 032 in REE patterns, but have higher concentrations of Al₂O₃. Ar‐Ar step release results are complex, but yield a whole‐rock age of ?2.8 Ga, suggesting that NWA 032 was extruded at 2.8 Ga or earlier. This rock may be the youngest sample of mare basalt collected to date. Noble gas concentrations combined with previously collected radionuclide data indicate that the meteorite exposure history is distinct from currently recognized lunar meteorites. In short, the geochemical and petrographic features of NWA 032 are not matched by Apollo or Luna samples, nor by previously identified lunar meteorites, indicating that it originates from a previously unsampled mare deposit. Detailed assessment of petrographic features, olivine zoning, and thermodynamic modelling indicate a relatively simple cooling and crystallization history for NWA 032. Chromite‐spinel, olivine, and pyroxene crystallized as phenocrysts while the magma cooled no faster than 2 °C/h based on the polyhedral morphology of olivine. Comparison of olivine size with crystal growth rates and preserved Fe‐Mg diffusion profiles in olivine phenocrysts suggest that olivine was immersed in the melt for no more than 40 days. Plumose textures in groundmass pyroxene, feldspar, and ilmenite, and Fe‐rich rims on the phenocrysts formed during rapid crystallization (cooling rates ?20 to 60 °C/h) after eruption.     

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.     

Primitive olivine‐phyric shergottite NWA 5789: Petrography,mineral chemistry,and cooling history imply a magma similar to Yamato‐980459

Knowledge of Martian igneous basaltic compositions is crucial for constraining mantle evolution, including early differentiation and mantle convection. Primitive magmas provide direct information about their mantle source regions, but most Martian meteorites either contain cumulate olivine or crystallized from fractionated melts. The recently discovered Martian meteorite Northwest Africa (NWA) 5789 is an olivine‐phyric shergottite. NWA 5789 has special significance among the Martian meteorites because it appears to represent one of the most magnesian Martian magmas known, other than Yamato (Y) 980459. Its most magnesian olivine cores (Fo₈₅) are in Mg‐Fe equilibrium with a magma of the bulk rock composition, suggesting that the bulk represents a magma composition. Based on the Al/Ti ratio of its pyroxenes, we infer that the rock began to crystallize at a high pressure consistent with conditions in Mars’ lower crust/upper mantle. It continued and completed its crystallization closer to the surface, where cooling was rapid and produced a mesostasis of radiating sprays of plagioclase and pyroxene. The mineralogy, petrology, mineral chemistry, and bulk rock composition of NWA 5789 are very similar to those of Y‐980459. The similarities between the two meteorites suggest that NWA 5789 (like Y‐980459) represents a primitive, mantle‐derived magma composition. They also suggest the possibility that NWA 5789 and Y‐980459 formed in the same lava flow. However, based on the mineralogy and texture of its mesostasis, NWA 5789 must have cooled more slowly than Y‐980459. NWA 5789 will help elucidate the igneous geology and geochemistry of Mars.     

Effect of chlorine on near‐liquidus crystallization of olivine‐phyric shergottite NWA 6234 at 1 GPa: Implication for volatile‐induced melting of the Martian mantle

Martian magmas are thought to be rich in chlorine compared with their terrestrial counterparts. Here, we experimentally investigate the effect of chlorine on liquidus depression and near‐liquidus crystallization of olivine‐phyric shergottite NWA 6234 and compare these results with previous experimental results on the effect of chlorine on near‐liquidus crystallization of the surface basalts Humphrey and Fastball. Previous experimental results showed that the change in liquidus temperature is dependent on the bulk composition of the basalt. The effect of chlorine on liquidus depression is greater for lower SiO₂ and higher Al₂O₃ magmas than for higher SiO₂ and lower Al₂O₃ magmas. The bulk composition for this study has lower Al₂O₃ and higher FeO contents than previous work; therefore, we provide additional constraints on the effect of the bulk composition on the influence of chlorine on near‐liquidus crystallization. High pressure and temperature crystallization experiments were performed at 1 GPa on a synthetic basalt, of the bulk composition of NWA 6234, with 0–4 wt% Cl added to the sample as AgCl. The results are consistent with previous notions that with increasing wt% Cl in the melt, the crystallization temperature decreases. Importantly, our results have a liquidus depression ?T (°C) from added chlorine that is consistent with the difference in bulk composition and suggest a dependence on both the bulk Al₂O₃ and FeO content. Our results suggest that the addition of chlorine to the Martian mantle may lower magma genesis temperatures and potentially aid in the petrogenesis of Martian magmas.     

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.     

Major element and primary sulfur concentrations in Apollo 12 mare basalts: The view from melt inclusions

Abstract— Major element and sulfur concentrations have been determined in experimentally heated olivine‐hosted melt inclusions from a suite of Apollo 12 picritic basalts (samples 12009, 12075, 12020, 12018, 12040, 12035). These lunar basalts are likely to be genetically related by olivine accumulation (Walker et al. 1976a, b). Our results show that major element compositions of melt inclusions from samples 12009, 12075, and 12020 follow model crystallization trends from a parental liquid similar in composition to whole rock sample 12009, thereby partially confirming the olivine accumulation hypothesis. In contrast, the compositions of melt inclusions from samples 12018, 12040, and 12035 fall away from model crystallization trends, suggesting that these samples crystallized from melts compositionally distinct from the 12009 parent liquid and therefore may not be strictly cogenetic with other members of the Apollo 12 picritic basalt suite. Sulfur concentrations in melt inclusions hosted in early crystallized olivine (Fo₇₅) are consistent with a primary magmatic composition of 1050 ppm S, or about a factor of 2 greater than whole rock compositions with 400–600 ppm S. The Apollo 12 picritic basalt parental magma apparently experienced outgassing and loss of S during transport and eruption on the lunar surface. Even with the higher estimates of primary magmatic sulfur concentrations provided by the melt inclusions, the Apollo 12 picritic basalt magmas would have been undersaturated in sulfide in their mantle source regions and capable of transporting chalcophile elements from the lunar mantle to the surface. Therefore, the measured low concentration of chalcophile elements (e.g., Cu, Au, PGEs) in these lavas must be a primary feature of the lunar mantle and is not related to residual sulfide remaining in the mantle during melting. We estimate the sulfur concentration of the Apollo 12 mare basalt source regions to be ～75 ppm, which is significantly lower than that of the terrestrial mantle.     

Mineralogy and petrology of the LaPaz Icefield lunar mare basaltic meteorites

Abstract— Five basaltic meteorites from the LaPaz ice field are paired on the basis of their mineralogy and texture, and represent a unique basalt type distinct from those in the Apollo or Luna sample collections. LaPaz Icefield (LAP) 02205, LAP 02224, LAP 02226, LAP 02436 and LAP 03632 all contain plagioclase, pyroxene, ilmenite, spinel, olivine, and minor troilite, metal, phosphate, baddeleyite and silica (cristobalite). Brown glassy melt veins are ubiquitous and cross the primary igneous texture. Plagioclase, the major mineral and occurring as laths in a subophitic texture, is of narrow compositional range, from An_85–89. Pyroxene, also a major mineral, is strongly zoned, from augite and pigeonite cores to very iron‐rich rims. Ilmenite laths comprise approximately 3–5% of the basalts. Spinels show a large compositional range, comparable to that documented in Apollo 15 basalts, indicating an early chromite‐rich stage followed by an intermediate to late stage with Cr‐rich ulvöspinel. Relatively large, subhedral to skeletal olivine crystals (Fo_46–62) are sparse, and are too Forich to be in equilibrium with the bulk rock, indicating that these are xenocrysts rather than phenocrysts. The presence of melt veins with a similar composition to the bulk rock, maskelynitized plagioclase feldspar, and metastable cristobalite indicate that these rocks underwent significant shock, between 30 and 50 GPa. Calculated oxygen fugacity, using spinel‐ilmenite‐iron metal equilibria, is within the range defined by previous studies of lunar materials. The bulk composition (low MgO) and low calculated temperatures, together with modelling calculations, indicate an origin by fractional crystallization of a more primitive low TiO₂ parent liquid similar to Apollo 12 olivine basalt.     

The Hadley‐Apennine KREEP basalt igneous province

Abstract– We have studied 27 KREEP basalt fragments in six thin sections of samples collected from four Apollo 15 stations. Based on local geology and regional remote sensing data, these samples represent KREEP basalt lava flows that lie beneath the younger, local Apollo 15 mare basalts and under other mare flows north of the Apollo 15 site. Some of these rocks were deposited at the site as ejecta from the large craters Aristillus and Autolycus. KREEP basalts in this igneous province have a volume of 10³–2 × 10⁴ km³. Mineral and bulk compositional data indicate that the erupted magmas had Mg# [100 × molar Mg/(Mg + Fe)] up to 73, corresponding to orthopyroxene‐rich interior source regions with Mg# up to 90. Minor element variations in the parent magmas of the KREEP basalts, inferred from compositions of the most magnesian pyroxene and most calcic plagioclase in each sample, indicate small but significant differences in the concentrations of minor elements and Mg#, reflecting variations in the composition of lower crustal or mantle source regions and/or different amounts of partial melting of those source regions.     

Searching for nonlocal lithologies in the Apollo 12 regolith: A geochemical and petrological study of basaltic coarse fines from the Apollo lunar soil sample 12023,155

New data from a petrological and geochemical examination of 12 coarse basaltic fines from the Apollo 12 soil sample 12023,155 provide evidence of additional geochemical diversity at the landing site. In addition to the bulk chemical composition, major, minor, and trace element analyses of mineral phases are employed to ascertain how these samples relate to the Apollo 12 lithological basalt groups, thereby overcoming the problems of representativeness of small samples. All of the samples studied are low‐Ti basalts (0.9–5.7 wt% TiO₂), and many fall into the established olivine, pigeonite, and ilmenite classification of Apollo 12 basaltic suites. There are five exceptions: sample 12023,155_1A is mineralogically and compositionally distinct from other Apollo 12 basalt types, with low pigeonite REE concentrations and low Ni (41–55 ppm) and Mn (2400–2556 ppm) concentrations in olivine. Sample 12023,155_11A is also unique, with Fe‐rich mineral compositions and low bulk Mg# (=100 × atomic Mg/[Mg+Fe]) of 21.6. Sample 12023,155_7A has different plagioclase chemistry and crystallization trends as well as a wider range of olivine Mg# (34–55) compared with other Apollo 12 basalts, and shows greater similarities to Apollo 14 high‐Al basalts. Two other samples (12023,155_4A, and _5A) are similar to the Apollo 12 feldspathic basalt 12038, providing additional evidence that feldspathic basalts represent a lava flow proximal to the Apollo 12 site rather than material introduced by impacts. We suggest that at least one parent magma, and possibly as many as four separate parent magmas, are required in addition to the previously identified olivine, pigeonite, and ilmenite basaltic suites to account for the observed chemical diversity of basalts found in this study.     

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.     

Major and trace elements in igneous rocks from apollo 15

The concentrations of major and trace elements have been determined in igneous rocks from Apollo 15. All materials analyzed have typical depletions of Eu except for minerals separated from sample 15085. Four samples have concentrations of trace elements that are similar to those of KREEP. The samples of mare basalt from Apollo 15 have higher concentrations of FeO, MgO, Mn, and Cr and lower concentrations of CaO, Na₂O, K₂O, and rare-earth elements (REE) as compared to the samples of mare basalt from Apollos 11, 12, and 14. The samples can be divided into two groups on the basis of their normative compositions. One group is quartz normative and has low concentrations of FeO while the other is olivine normative and has high concentrations of FeO. The trace element data indicate that the samples of olivine normative basalt could be from different portions of a single lava flow. At least two and possible three parent magmas can be identified from the samples of the quartz normative group on the basis of their concentration ratios of Sm to Eu. Within each group, the compositions of the samples appear to be related by crystallization of olivine or pyroxene. Significant variations of the ratio of concentration of Sm to Eu cannot be produced without plagioclase-liquid equilibrium. The source material of mare basalt may be depleted in Eu. Alternatively, the magmas may have assimilated a small volume of material similar to KREEP.Paper dedicated to Prof. Harold C. Urey on the occasion of his 80th birthday on 29 April 1973.     

Pervasive shock melting at >65 GPa in a Martian basalt,the shergottite Northwest Africa 14672

Shergottites have provided abundant information on the volcanic and impact history of Mars. Northwest Africa (NWA) 14672 contributes to both of these aspects. It is a vesicular ophitic depleted olivine–phyric shergottite, with average plagioclase An₆₁Ab₃₉Or_0.2. It is highly ferroan, with pigeonite compositions En_49-25Fs_41-61Wo_10-14 like those of basaltic shergottites, for example, NWA 12335. Olivine (Fo_53-15) has discrete ferroan overgrowths, more ferroan when in contact with plagioclase than when enclosed by pyroxene. The pyroxene (a continuum of augite, subcalcic augite, and pigeonite) is patchy, with ragged “cores” enveloped or invaded by ferroan pyroxene. Magma mixing may be responsible for capture of olivine and formation of pyroxene mantles. The plagioclase is maskelynite-like in appearance, but the original laths were (congruently) melted and the melt partly crystallized as fine dendrites. Most of the 14% vesicles occur within plagioclase. Olivine, pyroxene, and ilmenite occur in part as fine aggregates crystallized after congruent melting with limited subsequent liquid mixing. There are two fine-grained melt components, barred plagioclase with interstitial Fe-bearing phases, and glass with olivine dendrites, derived by melting of mainly plagioclase and mainly pyroxene, respectively. Rare silica particles contain coesite and/or quartz, and silica glass. The rock has experienced >50% melting, compatible with peak pressure >~65 GPa. It is the most highly shocked shergottite so far, at shock stage S6/7. It may belong to the group of depleted shergottites ejected at ~1 Myr from Tooting Crater.     

Heavily metamorphosed clasts from the CV chondrite breccias Mokoia and Yamato‐86009

Abstract– Metamorphosed clasts in the CV carbonaceous chondrite breccias Mokoia and Yamato‐86009 (Y‐86009) are coarse‐grained, granular, polymineralic rocks composed of Ca‐bearing (up to 0.6 wt% CaO) ferroan olivine (Fa_34–39), ferroan Al‐diopside (Fs_9–13Wo_47–50, approximately 2–7 wt% Al₂O₃), plagioclase (An_37–84Ab_63–17), Cr‐spinel (Cr/(Cr + Al) = 0.19–0.45, Fe/(Fe + Mg) = 0.60–0.79), nepheline, pyrrhotite, pentlandite, Ca‐phosphate, and rare grains of Ni‐rich taenite; low‐Ca pyroxene is absent. Most clasts have triple junctions between silicate grains, indicative of prolonged thermal annealing. Based on the olivine‐spinel and pyroxene thermometry, the estimated metamorphic temperature recorded by the clasts is approximately 1100 K. Few clasts experienced thermal metamorphism to a lower degree and preserved chondrule‐like textures. The Mokoia and Y‐86009 clasts are mineralogically unique and different from metamorphosed chondrites of known groups (H, L, LL, R, EH, EL, CO, CK) and primitive achondrites (acapulcoites, brachinites, lodranites). On a three‐isotope oxygen diagram, compositions of olivine in the clasts plot along carbonaceous chondrite anhydrous mineral line and the Allende mass‐fractionation line, and overlap with those of the CV chondrule olivines; the Δ¹⁷O values of the clasts range from about ?4.3‰ to ?3.0‰. We suggest that the clasts represent fragments of the CV‐like material that experienced metasomatic alteration, high‐temperature metamorphism, and possibly melting in the interior of the CV parent asteroid. The lack of low‐Ca pyroxene in the clasts could be due to its replacement by ferroan olivine during iron‐alkali metasomatic alteration or by high‐Ca ferroan pyroxene during melting under oxidizing conditions.     

Martian meteorite Tissint records unique petrogenesis among the depleted shergottites

Tissint, a new unaltered piece of Martian volcanic materials, is the most silica‐poor and Mg‐Fe‐rich igneous rock among the “depleted” olivine‐phyric shergottites. Fe‐Mg zoning of olivine suggests equilibrium growth (<0.1 °C h^?1) in the range of Fo_80–56 and olivine overgrowth (Fo_55–18) through a process of rapid disequilibrium (~1.0–5.0 °C h^?1). The spatially extended (up to 600 μm) flat‐top Fe‐Mg profiles of olivine indicates that the early‐stage cooling rate of Tissint was slower than the other shergottites. The chemically metastable outer rim of olivine (55) consists of oscillatory phosphorus zoning at the impact‐induced melt domains and grew rapidly compared to the early to intermediate‐stage crystallization of the Tissint bulk. High‐Ca pyroxene to low‐Ca pyroxene and high‐Ca pyroxene to plagioclase ratios of Tissint are more comparable to the enriched basaltic and enriched olivine‐phyric shergottites. Dominance of augite over plagioclase induced augite to control the Ca‐buffer in the residual melt suppressing the plagioclase crystallization, which also caused a profound effect on the Al‐content in the late‐crystallized pyroxenes. Mineral chemical stability, phase‐assemblage saturation, and pressure–temperature path of evolution indicates that the parent magma entered the solidus and left the liquidus field at a depth of 40–80 km in the upper mantle. Petrogenesis of Tissint appears to be similar to LAR 06319, an enriched olivine‐phyric shergottite, during the early to intermediate stage of crystallization. A severe shock‐induced deformation resulted in remelting (10–15 vol%), recrystallization (most Fe‐rich phases), and exhumation of Tissint in a time scale of 1–8 yr. Tissint possesses some distinct characteristics, e.g., impact‐induced melting and deformation, forming phosphorus‐rich recrystallization rims of olivine, and shock‐induced melt domains without relative enrichment of LREEs compared to the bulk; and shared characteristics, e.g., modal composition and magmatic evolution with the enriched basaltic shergottites, evidently reflecting unique mantle source in comparison to the clan of the depleted members.     

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.     

On the implications of an olivine dominated upper mantle on the development of a moon of fission origin

In a series of previous papers, a petrological model for the Moon has been developed based on the assumption that the Moon is a globe of differentiated terrestrial mantle material which fissioned from the Earth. One of the major constraints which this model matches is the hypothesis that the lunar upper mantle is dominated by pyroxene. However, it has been recently shown that olivine is most probably the major constituent of the lunar upper mantle and that, at least that part of the Moon has a composition which is very similar to that of pyrolite - the proposed composition of the Earth's mantle. As a result of this new model constraint, the previously proposed differentiation scheme for a Moon of fission origin is reviewed and found to be inadequate, despite modification, for explaining the near pyrolite composition of the lunar upper mantle. As a result, a solidification sequence, which has been proposed to explain the rhythmic banding in terrestrial ultra mafic complexes, is investigated and found to be able to account for the high olivine content of the upper mantle, assuming a pyrolite composition for the Moon.     

Chemical layering in the upper mantle of Mars: Evidence from olivine‐hosted melt inclusions in Tissint

Melting of Martian mantle, formation, and evolution of primary magma from the depleted mantle were previously modeled from experimental petrology and geochemical studies of Martian meteorites. Based on in situ major and trace element study of a range of olivine‐hosted melt inclusions in various stages of crystallization of Tissint, a depleted olivine–phyric shergottite, we further constrain different stages of depletion and enrichment in the depleted mantle source of the shergottite suite. Two types of melt inclusions were petrographically recognized. Type I melt inclusions occur in the megacrystic olivine core (Fo_76‐70), while type II melt inclusions are hosted by the outer mantle of the olivine (Fo_66‐55). REE‐plot indicates type I melt inclusions, which are unique because they represent the most depleted trace element data from the parent magmas of all the depleted shergottites, are an order of magnitude depleted compared to the type II melt inclusions. The absolute REE content of type II displays parallel trend but somewhat lower value than the Tissint whole‐rock. Model calculations indicate two‐stage mantle melting events followed by enrichment through mixing with a hypothetical residual melt from solidifying magma ocean. This resulted in ~10 times enrichment of incompatible trace elements from parent magma stage to the remaining melt after 45% crystallization, simulating the whole‐rock of Tissint. We rule out any assimilation due to crustal recycling into the upper mantle, as proposed by a recent study. Rather, we propose the presence of Al, Ca, Na, P, and REE‐rich layer at the shallower upper mantle above the depleted mantle source region during the geologic evolution of Mars.