Petrology of unique achondrite Queen Alexandra Range 93148: A piece of the pallasite (howardite‐eucrite‐diogenite?) parent body?

Abstract— Queen Alexandra Range (QUE) 93148 is a small (1.1 g) olivine‐rich achondrite (mg 86) that contains variable amounts of orthopyroxene (mg 87) and kamacite (6.7 wt% Ni), with minor augite. Olivine in QUE 93148 contains an unusual suite of inclusions: (1) 5 × 100 μm sized lamellae with a CaO‐ and Cr₂O₃‐rich (～10 and 22 wt%, respectively) composition that may represent a submicrometer‐scale intergrowth of chromite and pyroxene(s); (2) 75 × 500 μm sized lamellar symplectites composed of chromite and two pyroxenes, with minor metal; (3) 15–20 μm sized, irregularly‐shaped symplectites composed of chromite and pyroxene(s); (4) 100–150 μm sized, elliptical inclusions composed of chromite, two pyroxenes, metal, troilite, and rare whitlockite. Type 1, 2, and 3 inclusions probably formed by exsolution from the host olivine during slow cooling, whereas type 4 more likely resulted from early entrapment of silicate and metallic melts followed by closed‐system oxidation. Queen Alexandra Range 93148 can be distinguished from most other olivine‐rich achondrites (ureilites, winonaites, lodranites, acapulcoites, brachinites, Eagle‐Station‐type pallasites, and pyroxene pallasites), as well as from mesosiderites, by some or all of the following properties: O‐isotopic composition, Fe‐Mn‐Mg relations of olivine, CaO and Cr₂O₃ contents of olivine, orthopyroxene compositions, molar Cr/(Cr + Al) ratios of chromite, metal composition, texture, and the presence of the inclusions. In terms of many of these properties, it shows an affinity to main‐group pallasites. Nevertheless, it cannot be identified as belonging to this group. Meteorite QUE 93148 appears to be a unique achondrite. Possibly it should be considered to be a pyroxene pallasite that is genetically related to main‐group pallasites. Alternatively, it may be derived from the mantle of the pallasite (howardite‐eucrite‐diogenite?) parent body.     

Queen Alexandra Range 93148: A new type of pyroxene pallasite?

Abstract— Trace elements, including the rare earth elements, were measured in olivine and orthopyroxene from Queen Alexandra Range (QUE) 93148, and in olivine from two main group pallasites, Springwater and Mount Vernon. Although QUE 93148 was originally classified as a lodranite, a variety of data including oxygen isotopic compositions (Goodrich and Righter, 2000), preclude a genetic relationship with the acapulcoites/lodranites. Incompatible trace element (e.g., Ti, Zr) distributions in orthopyroxene do indicate large amounts of melting and are consistent with the ultramafic assemblage observed in this meteorite. Trace element abundances in olivine are consistent with suggestions that QUE 93148 may be related to the main group pallasites (Goodrich and Righter, 2000), although there are some inconsistencies. Its trace element distributions are most like those of the pyroxene pallasites, suggesting that it may have formed in a similar manner. QUE 93148 may represent a new type of pyroxene pallasite with links to the main group pallasites.     

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.     

Evolution of the winonaite parent body: Clues from silicate mineral trace element distributions

Abstract— We have measured the trace element compositions of individual plagioclase, pyroxene, and olivine grains in 6 different winonaites that span the range of textures and mineralogies observed in these meteorites. Textural evidence in these meteorites, including the presence of a plagioclase/clinopyroxene‐rich lithology and coarse‐grained olivine lithologies, suggests that they may have experienced some silicate partial melting. However, trace element distributions in these lithologies do not show any clear signatures for such an event. Pyroxene trace element compositions do exhibit systematic trends, with abundances generally lowest in Pontlyfni and highest in Winona. The fact that the same trends are present for both incompatible and compatible trace elements suggests, however, that the systematics are more likely the result of equilibration of minerals with initially heterogeneous and distinct compositions, rather than partial melting of a compositionally homogeneous precursor. The winonaites have experienced brecciation and mixing of lithologies, followed by varying degrees of thermal metamorphism on their parent body. These factors probably account for the variable bulk rare earth element (REE) patterns noted for these meteorites and may have led to re‐equilibration of trace elements in different lithologies.     

Minor element zoning and trace element geochemistry of pallasites

Abstract— I report here on an ion probe study of minor element spatial distributions and trace element concentrations in six pallasites. Pallasite olivines exhibit ubiquitous minor element zoning that is independent of grain size, morphology, and adjacent phases. Ca, Cr, Ti, V, and Ni concentrations decrease from center to rim by factors of up to 10, while Mn is generally unzoned or increases slightly at the very edge of some olivine grains. The maximum concentrations of these elements at the center of olivine vary from grain to grain within the same meteorite and among the pallasites studied. These zoning profiles are consistent with thermal diffusion during rapid cooling. The inferred cooling rates at high temperature regimes are orders of magnitude faster than the low‐temperature metallographic cooling rates (?0.5 to 2°C/Ma). This suggests that pallasites, like mesosiderites, have experienced rather complicated thermal histories, i.e., cooling rapidly at high temperatures and slowly at low temperatures. Pallasite olivines are essentially free of REEs. However, the phosphates display a wide range of REE abundances (0.001 to 100 x CI) with distinct patterns. REEs are generally homogeneous within a given grain but vary significantly from grain to grain by a factor of up to 100. Albin and Imilac whitlockite are highly enriched in HREEs (?50 x CI) but are relatively depleted in LREEs (?0.1 to 1 x CI). Eagle Station whitlockite has a very unusual REE pattern: flat LREEs at a 0.1 x CI level, a large positive Eu anomaly, and a sharp increase from Gd (0.1 x CI) to Lu (70 x CI). Eagle Station stanfieldite has a similar REE pattern to that of whitlockite but with much lower REEs by a factor of 10 to 100. Springwater farringtonite has relatively low REE concentrations (0.001 to 1 x CI) with a highly fractionated HREE‐enriched pattern (CI‐normalized Lu/La ?100). Postulating any igneous processes that could have fractionated REEs in these phosphates is difficult. Possibly, phosphates were incorporated into pallasites during mixing of olivine and IIIAB‐like molten Fe. These phosphates preserve characteristics of a previous history. Pallasites have not necessarily formed at the mantle‐core boundary of their parent bodies. The pallasite thermal histories suggest that pallasites may have formed at a shallow depth and were subsequently buried deep under a regolith blanket.     

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.     

Chondrule trace element geochemistry at the mineral scale

Abstract– We report trace element analyses from mineral phases in chondrules from carbonaceous chondrites (Vigarano, Renazzo, and Acfer 187), carried out by laser ablation inductively coupled plasma‐mass spectrometry. Results are similar in all three meteorites. Mesostasis has rare earth element (REE) concentrations of 10–20 × CI. Low‐Ca pyroxene has light REE (LREE) concentrations near 0.1 × CI and heavy REE (HREE) near 1 × CI, respectively. Olivine has HREE concentrations at 0.1–1 × CI and LREE around 10^?2 × CI. The coarsest olivine crystals tend to have the most fractionated REE patterns, indicative of equilibrium partitioning. Low‐Ca pyroxene in the most pyroxene‐rich chondrules tends to have the lowest REE concentrations. Type I chondrules seem to have undergone a significant degree of batch crystallization (as opposed to fractional crystallization), which requires cooling rates slower than 1–100 K h^?1. This would fill the gap between igneous calcium‐aluminum‐rich inclusions (CAIs) and type II chondrules. The anticorrelation between REE abundances and pyroxene mode may be understood as due to dilution by addition of silica to the chondrule melt, as in the gas‐melt interaction scenario of Libourel et al. (2006). The rapid cooling rate (of the order of 1000 K h^?1) which seems recorded by low‐Ca pyroxene, contrasted with the more diverse record of olivine, may point to a nonlinear cooling history or suggest that formation of pyroxene‐rich chondrule margins was an event distinct from the crystallization of the interior.     

In situ laser ablation ICP‐MS analyses of dimict diogenites: Further evidence for harzburgitic and orthopyroxenitic lithologies

Trace element concentrations in pyroxene, plagioclase, and olivine were measured in five diogenite breccias previously identified as containing distinct harzburgitic (ol+opx) and orthopyroxenitic (opx) lithologies (dimict). Three samples show two distinct populations of pyroxene trace element abundances, supporting their classification as dimict. These three meteorites show increases in Y, Yb, and HREE concentrations from harzburgitic to orthopyroxenitic pyroxenes, supporting the hypothesis that the lithologies are related through fractional crystallization whereby harzburgite olivine and pyroxene crystallized from the magma first followed by orthopyroxenite pyroxene. Depletions in LREE and Eu concentrations in the orthopyroxenitic lithology are most likely due to equilibration with LREE and Eu‐rich phases, likely plagioclase, which is found primarily in that lithology. Two samples do not show evidence supporting a dimict classification. Large pyroxene trace element variation in one sample indicates that it is polymict, while uniform trace element distribution in the other suggests that it may be a monomict breccia.     

Characterization of weathering and heterogeneous mineral phase distribution in brachinite Northwest Africa 4872

Terrestrial weathering of hot desert achondrite meteorite finds and heterogeneous phase distributions in meteorites can complicate interpretation of petrological and geochemical information regarding parent‐body processes. For example, understanding the effects of weathering is important for establishing chalcophile and siderophile element distributions within sulfide and metal phases in meteorites. Heterogeneous mineral phase distribution in relatively coarsely grained meteorites can also lead to uncertainties relating to compositional representativeness. Here, we investigate the weathering and high‐density (e.g., sulfide, spinel, Fe‐oxide) phase distribution in sections of ultramafic achondrite meteorite Northwest Africa (NWA) 4872. NWA 4872 is an olivine‐rich brachinite (Fo_{63.6 ± 0.5}) with subsidiary pyroxene (Fs_9.7 ± 0.1Wo_{46.3 ± 0.2}), Cr‐spinel (Cr# = 70.3 ± 1.1), and weathered sulfide and metal. Raman mapping confirms that weathering has redistributed sulfur from primary troilite, resulting in the formation of Fe‐oxide (‐hydroxide) and marcasite (FeS₂). From Raman mapping, NWA 4872 is composed of olivine (89%), Ca‐rich pyroxene (0.4%), and Cr‐spinel (1.1%), with approximately 7% oxidized metal and sulfide and 2.3% marcasite‐dominated sulfide. Microcomputed tomography (micro‐CT) observations reveal high‐density regions, demonstrating heterogeneities in mineral distribution. Precision cutting of the largest high‐density region revealed a single 2 mm Cr‐spinel grain. Despite the weathering in NWA 4872, rare earth element (REE) abundances of pyroxene determined by laser‐ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) indicate negligible modification of these elements in this mineral phase. The REE abundances of mineral grains in NWA 4872 are consistent with formation of the meteorite as the residuum of the partial melting process that occurred on its parent body. LA‐ICP‐MS analyses of sulfide and alteration products demonstrate the mobility of Re and/or Os; however, highly siderophile element (HSE) abundance patterns remain faithful recorders of processes acting on the brachinite parent body(ies). Detailed study of weathering and phase distribution offers a powerful tool for assessing the effects of low‐temperature alteration and for identifying robust evidence for parent‐body processes.     

Cosmic‐ray exposure ages of pallasites

We analyzed cosmogenic nuclides in metal and/or silicate (primarily olivine) separated from the main‐group pallasites Admire, Ahumada, Albin, Brahin, Brenham, Esquel, Finmarken, Glorieta Mountain, Huckitta, Imilac, Krasnojarsk, Marjalahti, Molong, Seymchan, South Bend, Springwater, and Thiel Mountains and from Eagle Station. The metal separates contained an olivine fraction which although small, <1 wt% in most cases, nonetheless contributes significantly to the budgets of some nuclides (e.g., up to 35% for ²¹Ne and ²⁶Al). A correction for olivine is therefore essential and was made using model calculations and/or empirical relations for the production rates of cosmogenic nuclides in iron meteoroids and/or measured elemental concentrations. Cosmic‐ray exposure (CRE) ages for the metal phases of the main‐group pallasites range from 7 to 180 Ma, but many of the ages cluster around a central peak near 100 Ma. These CRE ages suggest that the parent body of the main‐group pallasites underwent a major break‐up that produced most of the meteorites analyzed. The CRE age distribution for the pallasites overlaps only a small fraction of the distribution for the IIIAB iron meteorites. Most pallasites and IIIAB irons originated in different collisions, probably on different parent bodies; a few IIIABs and pallasites may have come out of the same collision but a firm conclusion requires further study. CRE ages calculated from noble gas and radionuclide data of the metal fraction are higher on average than the ²¹Ne exposure ages obtained for the olivine samples. As the metal and olivine fractions were taken in most cases from different specimens, the depth‐dependency of the production rate ratio ¹⁰Be/²¹Ne in metal, not accounted for in our calculations, may explain the difference.     

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.     

Petrology and geochemistry of the Northwest Africa 3368 eucrite

Abstract– Analysis of the mineralogy, isotopic, and bulk compositions of the eucrite meteorites is imperative for understanding their origin on the asteroid 4 Vesta, the proposed parent body of the HED meteorites. We present here the petrology, mineral compositions, and bulk chemistry of several lithic components of the new brecciated basaltic eucrite Northwest Africa (NWA) 3368 to determine if all the lithologies reflect formation from one rock type or many rock types. The meteorite has three main lithologies: coarse‐ and fine‐grained clasts surrounded by a fine‐grained recrystallized silicate matrix. Silicate compositions are homogeneous, and the average rare earth element pattern for NWA 3368 is approximately 10× CI chondrites with a slight negative Eu anomaly. Major and trace element data place NWA 3368 with the Main Group‐Nuevo Laredo trend. High‐Ti chromites with ilmenite exsolution lamellae provide evidence of NWA 3368’s history of intense metamorphism. We suggest that this meteorite underwent several episodes of brecciation and metamorphism, similar to that proposed by Metzler et al. (1995) . We conclude that NWA 3368 is a monomict basaltic eucrite breccia related to known eucrites in texture and in mineral, bulk, and oxygen isotopic composition.     

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

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

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.     

Mbosi: An anomalous iron with unique silicate inclusions

Abstract— The Mbosi iron meteorite contains millimeter size silicate inclusions. Mbosi is an ungrouped iron meteorite with a Ge/Ga ratio >10, which is an anomalous property shared with the five-member IIF iron group, the Eagle Station pallasites and four other ungrouped irons. Neither the IIF group nor the four other ungrouped irons are known to have silicate inclusions. Chips from three Mbosi inclusions were studied, but most of the work concentrated on a whole 3.1 mm circular inclusion. This inclusion consists of a mantle and a central core of different mineralogies. The mantle is partially devitrified quartz-normative glass, consisting of microscopic crystallites of two pyroxenes and plagioclase, which are crystalline enough to give an x-ray powder diffraction pattern but not coarse enough to permit analyses of individual minerals. The core consists of silica. The bulk composition does not match any known meteorite type, although there is a similarity in mode of occurrence to quartz-normative silicate inclusions in some HE irons. Mbosi silicate appears to be unique. The bulk rare earth element (REE) pattern of the mantle is flat at ? 7×C1; the core is depleted in REE but shows a small positive Eu anomaly. The O-isotope composition of bulk silicate lies on a unit slope mixing line (parallel and close to the C3 mixing line) that includes the Eagle Station pallasites and the iron Bocaiuva (related to the IIF irons); all of these share the property of having Ge/Ga ratios >10. It is concluded that Mbosi silicate represents a silica-bearing source rock that was melted and injected into metal. Melting occurred early in the history of the parent body because the metal now shows a normal Widmanstätten structure with only minor distortion that was caused when the parent body broke up and released meteorites into interplanetary space. The cause of Ge/Ga ratios being >10 in these irons is unknown. The fact that silicates in Mbosi, Bocaiuva (related to IIF irons) and the Eagle Station trio of pallasites, all characterized by a Ge/Ga ratio >10, lie on a unit slope mixing line in the O-isotope diagram suggests that their origins are closely related. The C3 chondrites appear to be likely precursors for silicates in Mbosi, Bocaiuva and the Eagle Station pallasites.     

FeO‐rich silicates in the Sahara 97159 (EH3) enstatite chondrite: Mineralogy,oxygen isotopic compositions,and origin

Abstract— We report the mineralogy and oxygen isotopic compositions of FeO‐rich silicates in the Sahara 97159 EH3 chondrite. This component is referred to as FeO‐rich because it contains substantially more FeO than the characteristic FeO‐poor silicates in the highly reduced enstatite meteorites. These FeO‐rich silicates are mostly low‐Ca pyroxene (Fs5–35) and their compositions suggest an origin under more oxidizing conditions, like those for the ordinary chondrites. However, the mafic silicates in ordinary and carbonaceous chondrites are dominantly olivine, and the FeO‐rich silicates in the E chondrites are less commonly olivine. The oxygen isotopic compositions of the FeO‐rich silicates are indistinguishable from those of FeO‐poor silicates in Sahara 97159. These observations suggest that both the FeO‐rich silicates and the FeO‐poor silicates in EH chondrites formed from the same oxygen reservoir where redox conditions varied widely.     

Relationship between positive cerium anomaly and adsorbed water in Antarctic lunar meteorites

Abstract— Concentrations of adsorbed water in single mineral grains of Antarctic lunar meteorites were determined with micro infrared (IR) spectroscopy. A relationship was found between the mineral's ability to adsorb water and the extent of Ce anomaly in rare earth element (REE) patterns precisely determined by the isotope dilution method using a thermal ionization mass spectrometer. Asuka (A) 881757, a lunar meteorite from the mare basalt without Ce anomaly, showed no trace of IR absorption due to adsorbed water. On the contrary, Yamato (Y) 791197-109, Y-86032-98, Y-86032-95, Y-791197-115 and Y-82192-55A from the lunar highland exhibiting positive Ce anomaly showed IR absorption due to adsorbed water in some of their minerals. The detected water would be of terrestrial origin, because it was not structurally bound and easy to exchange judging from the spectral band shape. The contrast in concentration of adsorbed water between the lunar highland and the mare basalt is derived from a difference in the density of microfractures in mineral grains. Average concentrations of adsorbed water in the lunar highland meteorites were 3.8 mg/cm³ for pyroxene and olivine, and 1.7 mg/cm³ for plagioclase. This contrast between minerals is noteworthy because it has been known that Ce anomaly of pyroxene and olivine is larger than that of plagioclase both for Antarctic lunar meteorites and some lunar rocks. Furthermore, more adsorbed water was detected for minerals in meteorites that exhibit larger Ce anomaly. The present observations demonstrate that the extent of Ce anomaly correlated with the concentration of adsorbed water, which suggests that active mineral surface resulting in adsorption of water could be a trace of interaction forming Ce anomaly. Terrestrial weathering on Antarctica and REE fractionation on the Moon are discussed for possible origins of the Ce anomaly.     

Chondrule heritage and thermal histories from trace element and oxygen isotope analyses of chondrules and amoeboid olivine aggregates

We report combined oxygen isotope and mineral‐scale trace element analyses of amoeboid olivine aggregates (AOA) and chondrules in ungrouped carbonaceous chondrite, Northwest Africa 5958. The trace element geochemistry of olivine in AOA, for the first time measured by LA‐ICP‐MS, is consistent with a condensation origin, although the shallow slope of its rare earth element (REE) pattern is yet to be physically explained. Ferromagnesian silicates in type I chondrules resemble those in other carbonaceous chondrites both geochemically and isotopically, and we find a correlation between ¹⁶O enrichment and many incompatible elements in olivine. The variation in incompatible element concentrations may relate to varying amounts of olivine crystallization during a subisothermal stage of chondrule‐forming events, the duration of which may be anticorrelated with the local solid/gas ratio if this was the determinant of oxygen isotopic ratios as proposed recently. While aqueous alteration has depleted many chondrule mesostases in REE, some chondrules show recognizable subdued group II‐like patterns supporting the idea that the immediate precursors of chondrules were nebular condensates.     

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.