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.     

Spinel assemblages in lunar meteorites Graves Nunataks 06157 and Dhofar 1528: Implications for impact melting and equilibration in the Moon's upper mantle

Magnesium‐rich spinel assemblages occur in the two lunar vitric breccia meteorites—Dhofar (Dho) 1528 and Graves Nunataks (GRA) 06157. Dho 1528 contains up to ~0.7 mm cumulate Mg‐rich spinel crystals associated with Mg‐rich olivine, Mg‐ and Al‐rich pyroxene, plagioclase, and rare cordierite. Using thermodynamic calculations of these mineral assemblages, we constrain equilibration depths and discuss an origin of these lithologies in the upper mantle of the Moon. In contrast, small, 10 to 20 μm spinel phenocryst assemblages in glassy melt rock clasts in Dho 1528 and GRA 06157 formed from the impact melting of Mg‐rich rocks. Some of these spinel phenocrysts match compositional constraints for spinel associated with “pink spinel anorthosites” inferred from remote sensing data. However, such spinel phenocrysts in meteorites and Apollo samples are typically associated with significant amounts of olivine ± pyroxene that exceed the compositional constraints for pink spinel anorthosites. We conclude that the remotely sensed “pink spinel anorthosites” have not been observed in the collections of lunar rocks. Moreover, we discuss impact‐excavation scenarios for the spinel‐bearing assemblages in Dhofar 1528 and compare the bulk rock composition of Dho 1528 to strikingly similar compositions of Luna 20 samples that contain ejecta from the Crisium impact basin.     

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

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

The pyroxene pallasites,Vermillion and Yamato 8451: Not quite a couple

Abstract— Two pallasites, Vermillion and Yamato (Y)‐8451, have been studied to obtain petrologic, trace element, and O‐isotopic data. Both meteorites contain low‐Ca and high‐Ca pyroxenes (<2% by volume) and have been dubbed “pyroxene pallasites.” Pyroxene occurs as large individual grains, as inclusions in olivine and in other pyroxene, and as grains along the edges of olivine. Symplectic overgrowths, sometimes found in Main Group and Eagle Station pallasites, are not seen in the pyroxene pallasites. Olivine compositions are Fa_10–12, similar to those of Main Group pallasites. Siderophile trace element data show that metal in the two meteorites have significantly differing compositions that are, for many elements, outside the range of the Main Group and Eagle Station pallasites. These compositions also differ from those of IAB and IIIAB iron meteorites. Rare earth element (REE) patterns in merrillite are similar to those seen in other pallasites, indicating formation by subsolidus reaction between metal and silicate, with the merrillite inheriting its pattern from the surrounding silicates. The O‐isotopic compositions of Vermillion and Y‐8451 are similar but differ from Main Group or Eagle Station pallasites, as well as other achondrite and primitive achondrite groups. Although Vermillion and Y‐8451 have similar mineralogy, pyroxene compositions, REE patterns, and O‐isotopic compositions, there is sufficient evidence to resist formally grouping these two meteorites. This evidence includes the texture of Vermillion, siderophile trace element data, and the presence of cohenite in Vermillion.     

Petrogenesis of anomalous Queen Alexandra Range enstatite meteorites and their relation to enstatite chondrites,primitive enstatite achondrites,and aubrites

Queen Alexandra Range (QUE) meteorite 94204 is an anomalous enstatite meteorite whose petrogenesis has been ascribed to either partial melting or impact melting. We studied the meteorite pairs QUE 94204, 97289/97348, 99059/99122/99157/99158/99387, and Yamato (Y)‐793225; these were previously suggested to represent a new grouplet. We present new data for mineral abundances, mineral chemistries, and siderophile trace element compositions (of Fe,Ni metal) in these meteorites. We find that the texture and composition of Y‐793225 are related to EL6, and that this meteorite is unrelated to the QUEs. The mineralogy and siderophile element compositions of the QUEs are consistent with petrogenesis from an enstatite chondrite precursor. We caution that potential re‐equilibration during melting and recrystallization of enstatite chondrite melt‐rocks make it unreliable to use mineral chemistries to assign a specific parent body affinity (i.e., EH or EL). The QUEs have similar mineral chemistries among themselves, while slight variations in texture and modal abundances exist between them. They are dominated by inclusion‐bearing millimeter‐sized enstatite (average En_99.1–99.5) with interstitial spaces filled predominantly by oligoclase feldspar (sometimes zoned), kamacite (Si approximately 2.4 wt%), troilite (≤2.4 wt% Ti), and cristobalite. Siderophile elements that partition compatibly between solid metal and liquid metal are not enriched like in partial melt residues Itqiy and Northwest Africa (NWA) 2526. We find that the modal compositions of the QUEs are broadly unfractionated with respect to enstatite chondrites. We conclude that a petrogenesis by impact melting, not partial melting, is most consistent with our observations.     

Compositional constraints on the genesis of diogenites

Abstract– We have done bulk rock compositional analyses (INAA, ICP‐MS) and petrologic study of a suite of diogenite meteorites. Most contain orthopyroxenes with mg#s of 70.6–79.0. Meteorite Hills (MET) 00425 is magnesian (mg# of 83.9). Lewis Cliff (LEW) 88011 contains orthopyroxene grains of varying mg# (76.3–68.6). Queen Alexandra Range (QUE) 93009 (orthopyroxene mg# 70.6) contains coarse‐grained noritic clasts (plagioclase An_84.7–88.3), and is rich in incompatible trace elements. It has Eu/Eu* < 1, indicating that cumulate norites do not dominate its trace element inventory. Queen Alexandra Range 93009 may be transitional between diogenites and magnesian cumulate eucrites. Lewis Cliff 88679, a dimict breccia of harzburgite and orthopyroxenite, has anomalously low concentrations of highly incompatible elements (e.g., Nb, La, Ta, U) compared to other diogenites, but is similar to them in less highly incompatible elements (e.g., Y, Zr, Yb, Hf). It is unlikely that this characteristic reflects a low proportion of a trapped melt component. The highly incompatible elements were likely mobilized after impact mixing of the two parent lithologies. Graves Nunataks 98108 shows an extreme range in Eu/Eu* attributable to the heterogeneous distribution of plagioclase; one sample has the lowest Eu/Eu* among diogenites. We find no compelling evidence to support the hypothesis that diogenite parent magmas were contaminated by partial melts of the eucritic crust. We posit that subsolidus equilibration between orthopyroxene and minor/trace phases (including phosphates) resulted in preferential redistribution of Eu²⁺ relative to Eu³⁺ and other rare earth elements, and results in anomalously low Eu/Eu* in samples leached in acids that dissolve phosphates.     

Geochemical diversity of shergottite basalts: Mixing and fractionation,and their relation to Mars surface basalts

The chemical compositions of shergottite meteorites, basaltic rocks from Mars, provide a broad view of the origins and differentiation of these Martian magmas. The shergottite basalts are subdivided based on their Al contents: high‐Al basalts (Al > 5% wt) are distinct from low‐Al basalts and olivine‐phyric basalts (both with Al < 4.5% wt). Abundance ratios of highly incompatible elements (e.g., Th, La) are comparable in all the shergottites. Abundances of less incompatible elements (e.g., Ti, Lu, Hf) in olivine‐phyric and low‐Al basalts correlate well with each other, but the element abundance ratios are not constant; this suggests mixing between components, both depleted and enriched. High‐Al shergottites deviate from these trends consistent with silicate mineral fractionation. The “depleted” component is similar to the Yamato‐980459 magma; approximately, 67% crystal fractionation of this magma would yield a melt with trace element abundances like QUE 94201. The “enriched” component is like the parent magma for NWA 1068; approximately, 30% crystal fractionation from it would yield a melt with trace element abundances like the Los Angeles shergottite. This component mixing is consistent with radiogenic isotope and oxygen fugacity data. These mixing relations are consistent with the compositions of many of the Gusev crater basalts analyzed on Mars by the Spirit rover (although with only a few elements to compare). Other Mars basalts fall off the mixing relations (e.g., Wishstone at Gusev, Gale crater rocks). Their compositions imply that basalt source areas in Mars include significant complexities that are not present in the source areas for the shergottite basalts.     

The Divnoe meteorite: Petrology,chemistry, oxygen isotopes and origin

Abstract— The Divnoe meteorite is an olivine-rich primitive achondrite with subchondritic chemistry and mineralogy. It has a granoblastic, coarse-grained, olivine groundmass (CGL: coarse-grained lithology) with relatively large pyroxene-plagioclase poikilitic patches (PP) and small fine-grained domains of an opaque-rich lithology (ORL). Both PP and ORL are inhomogeneously distributed and display reaction boundaries with the groundmass. Major silicates, olivine (Fa_20–28) and orthopyroxene (Fs_20–28 Wo_0.5–2.5), display systematic differences in composition between CGL and ORL as well as a complicated pattern of variations within CGL. Accessory plagioclase has low K content and displays regular igneous zoning with core compositions An_40–45 and rims An_32–37. The bulk chemical composition of Divnoe is similar to that of olivine-rich primitive achondrites, except for a depletion of incompatible elements and minor enrichment of refractory siderophiles. Oxygen isotope compositions for whole-rock and separated minerals from Divnoe fall in a narrow range, with mean δ¹⁸O = +4.91, δ¹⁷O = +2.24, and Δ¹⁷O = ?0.26 ± 0.11. The isotopic composition is not within the range of any previously recognized group but is very close to that of the brachinites. To understand the origin of Divnoe lithologies, partial melting and crystallization were modelled using starting compositions equal to that of Divnoe and some chondritic meteorites. It was found that the Divnoe composition could be derived from a chondritic source region by ～20 wt% partial melting at T ～ 1300 °C and log(fO₂) = IW-1.8, followed by ～60 wt% crystallization of the partial melt formed, and removal of the still-liquid portion of the partial melt. Removal of the last partial melt resulted in depletion of the Divnoe plagioclase in Na and K. In this scenario, CGL represents the residue of partial melting, and PP is a portion of the partial melt that crystallized in situ. The ORL was formed during the final stages of partial melting by reaction between gaseous sulfur and residual olivine in the source region. A prominent feature of Divnoe is fine μm-scale chemical variations within olivine grains, related to lamellar structures the olivines display. The origin of these structures is not known.     

The Antarctic achondrite,Grove Mountains 021663: An olivine‐rich winonaite

Abstract– The Grove Mountains (GRV) 021663 meteorite was collected from the Grove Mountains region of Antarctica. The meteorite is composed primarily of olivine (Fa_5.4), orthopyroxene (Fs_4.7Wo_3.0), chromian diopside (En_53.6Fs_2.4Wo₄₄), troilite, kamacite, and plagioclase (Ab_74.5Or₄An_21.5). Minor phases include schreibersite and K‐feldspar. The meteorite is highly weathered (W3) and weakly shocked (S2). We determine a whole rock oxygen isotopic composition of δ¹⁸O = 7.50‰, δ¹⁷O = 3.52‰. Comparisons of these data with other primitive achondrites have resulted in the reclassification of this meteorite as a member of the winonaite group. The occurrences of troilite, metal, and schreibersite in GRV 021663 indicate that these minerals were once completely molten. Euhedral inclusions of pyroxene within plagioclase further suggest that these may have crystallized from a silicate melt, while the depletion of plagioclase, metal, and troilite indicates that GRV 021663 could represent a residuum following partial melting on its parent asteroid. Trace element distributions in silicate minerals do not, however, confirm this scenario. As with other winonaite meteorites, the formation of GRV 021663 probably relates to brecciation and mixing of heterogeneous lithologies, followed by varying degrees of thermal metamorphism on the parent body asteroid. Peak metamorphic conditions may have resulted in localized partial melting of metal and silicate mineralogies, but our data are not conclusive.     

Differentiation processes in FeO‐rich asteroids revealed by the achondrite Lewis Cliff 88763

Olivine‐dominated (70–80 modal %) achondrite meteorite Lewis Cliff (LEW) 88763 originated from metamorphism and limited partial melting of a FeO‐rich parent body. The meteorite experienced some alteration on Earth, evident from subchondritic Re/Os, and redistribution of rhenium within the sample. LEW 88763 is texturally similar to winonaites, has a Δ¹⁷O value of ?1.19 ± 0.10‰, and low bulk‐rock Mg/(Mg+Fe) (0.39), similar to the FeO‐rich cumulate achondrite Northwest Africa (NWA) 6693. The similar bulk‐rock major‐, minor‐, and trace‐element abundances of LEW 88763, relative to some carbonaceous chondrites, including ratios of Pd/Os, Pt/Os, Ir/Os, and ¹⁸⁷Os/¹⁸⁸Os (0.1262), implies a FeO‐ and volatile‐rich precursor composition. Lack of fractionation of the rare earth elements, but a factor of approximately two lower highly siderophile element abundances in LEW 88763, compared with chondrites, implies limited loss of Fe‐Ni‐S melts during metamorphism and anatexis. These results support the generation of high Fe/Mg, sulfide, and/or metal‐rich partial melts from FeO‐rich parent bodies during partial melting. In detail, however, LEW 88763 cannot be a parent composition to any other meteorite sample, due to highly limited silicate melt loss (0 to <<5%). As such, LEW 88763 represents the least‐modified FeO‐rich achondrite source composition recognized to date and is distinct from all other meteorites. LEW 88763 should be reclassified as an anomalous achondrite that experienced limited Fe,Ni‐FeS melt loss. Lewis Cliff 88763, combined with a growing collection of FeO‐rich meteorites, such as brachinites, brachinite‐like achondrites, the Graves Nunataks (GRA) 06128/9 meteorites, NWA 6693, and Tafassasset, has important implications for understanding the initiation of planetary differentiation. Specifically, regardless of precursor compositions, partial melting and differentiation processes appear to be similar on asteroidal bodies spanning a range of initial oxidation states and volatile contents.     

Glasses in howardites: Impact melts or pyroclasts?

We have analyzed glasses in eight howardites with the aim of distinguishing their origins as impact melts or pyroclasts. Although theoretical calculations predict that pyroclastic eruptions could have taken place on Vesta, the occurrence of pyroclastic glasses in HED meteorites has not been documented. This study involved petrographic examination of textures, electron microprobe analysis of major and minor elements, and LA‐ICP‐MS analysis for selected trace elements. Previously documented textural and compositional differences between lunar impact‐melt and pyroclastic glasses partly guided this study. This work yielded no positive identification of pyroclastic glasses. The most likely explanation is that pyroclastic glasses never formed, either because Vesta contains insufficient volatiles to have powered explosive eruptions, or because eruptive conditions produced optically dense fire‐fountains that allowed melt drops to collect as lava ponds. The impact‐melt glasses were grouped (low‐alkali, Ca‐rich, and K‐rich) based on compositions. We suggest that these glasses are the result of impacts onto known HED lithologies. The low‐alkali glasses are impact melts of bulk HED lithologies. We hypothesize that the Ca‐rich and K‐rich glasses result from oversampling of plagioclase and of mesostasis that experienced liquid immiscibility, respectively, during micrometeorite impacts into eucrite targets.     

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

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

Redistribution of elements in the heavily shocked Yanzhuang chondrite

Abstract— Compositions of metal, sulfide, olivine, pyroxene, and plagioclase/plagioclase glass were studied for the melted and unmelted parts of the heavily shocked H6(S6) chondrite‐Yanzhuang. We found that the partitioning of some trace elements significantly changed between the 2 parts; compared with the corresponding minerals in the unmelted part, Ga is enriched in the metal, Co, Cr, and Zn are enriched in the sulfide, Cr is enriched in olivine and pyroxene, and Ti is enriched in the plagioclase glass of the melt pocket. These detailed studies of the mineral phases put constraints on 3 important parameters (temperature, pressure, and duration) associated with the post‐shock melting process. The coexistence of melted and unmelted olivine in the melt pocket of Yanzhuang implies a peak temperature after shock that approaches the melting point of olivine. The lack of Ni in the olivine crystallized from a melt suggests crystallization of olivine at pressures below 10 kbar. The resetting of Ga partitioning between metal and silicate in the melt pocket indicates that the interval from the peak temperature after shock to the crystallization of metal‐sulfide and plagioclase glass in the melted part of Yanzhuang is longer than 500 sec.     

Exploring the Moon's surface for remnants of the lunar mantle 1. Dunite xenoliths in mare basalts. A crustal or mantle origin?

Remotely sensed observations from recent missions (e.g., GRAIL, Kaguya, Chandrayaan‐1) have been interpreted as indicating that the deep crust and upper mantle are close to or at the lunar surface in many large impact basins (e.g., Crisium, Apollo, Moscoviense). If this is correct, the capability of either impact or volcanic processes to transport mantle lithologies to the lunar surface should be enhanced in these regions. Somewhat problematic to these observations and interpretations is that examples of mantle lithologies in the lunar sample collection (Apollo Program, Luna Program, lunar meteorites) are at best ambiguous. Dunite xenoliths in high‐Ti mare basalt 74275 are one of these ambiguous examples. In this high‐Ti mare basalt, olivine occurs in three generations: olivine associated with dunite xenoliths, olivine megacrysts, and olivine microphenocrysts. The dunite xenoliths are anhedral in shape and are generally greater than 800 μm in diameter. The interior of the xenoliths are fairly homogeneous with regard to many divalent cations. For example, the Mg# (Mg/Mg + Fe × 100) ranges from 82 to 83 in their interiors and decreases from 82 to 68 over the 10–30 μm wide outer rim. Titanium and phosphorus X‐ray maps of the xenolith illustrate that these slow diffusing elements preserve primary cumulate zoning textures. These textures indicate that the xenoliths consist of many individual olivine grains approximately 150–200 μm in diameter with low Ti, Al, and P cores. These highly incompatible elements are enriched in the outer Fe‐rich rims of the xenoliths and slightly enriched in the rims of the individual olivine grains. Highly compatible elements in olivine such as Ni exhibit a decrease in the rim surrounding the xenolith, an increase in the incompatible element depleted cores of the individual olivine grains, and a slight decrease in the “interior rims” of the individual olivine grains. Inferred melt composition, liquid lines of descent, and zoning profiles enable the reconstruction of the petrogenesis of the dunite xenoliths. Preservation of primary magmatic zoning (Ti, P, Al) and lack of textures similar to high‐pressure mineral assemblages exhibited by the Mg‐suite (Shearer et al. 2015) indicate that these xenoliths do not represent deep crustal or shallow mantle lithologies. Further, they are chemically and mineralogically distinct from Mg‐suite dunites identified from the Apollo 17 site. More likely, they represent olivine cumulates that crystallized from a low‐Ti mare basalt at intermediate to shallow crustal levels. The parent basalt to the dunite xenolith lithology was more primitive than low‐Ti basalts thus far returned from the Moon. Furthermore, this parental magma and its more evolved daughter magmas are not represented in the basalt sample suite returned from the Taurus‐Littrow Valley by the Apollo 17 mission. The dunite xenolith records several episodes of crystallization and re‐equilibration. During the last episode of re‐equilibration, the dunite cumulate was sampled by the 74275 high‐Ti basalt and transported over a period of 30–70 days to the lunar surface.     

Siderophile element characteristics of acapulcoite–lodranites and winonaites: Implications for the early differentiation processes of their parent bodies

We have studied magnetic fractions of five acapulcoites, three lodranites, and two winonaites to investigate chemical compositions of their precursor materials and metallic partial melting processes occurring on their parent bodies. One winonaite metal is similar in composition to low Au, low Ni IAB iron subgroup, indicating genetic relationship between them. Magnetic fractions of chondrule‐bearing acapulcoite and winonaite have intermediate chemical compositions of metals between H chondrites and EL chondrites. This fact indicates that the precursor materials of acapulcoite–lodranites and winonaites were similar to H and/or EL chondrites in chemical compositions. Magnetic fractions in acapulcoite–lodranites have a large variety of chemical compositions. Most of them show enrichments of W, Re, Ir, Pt, Mo, and Rh, and one of them shows clear depletion in Re and Ir relative to those of chondrule‐bearing acapulcoite. Chemical compositional variations among acapulcoite–lodranite metals cannot be explained by a single Fe‐Ni‐S partial melting event, but a two‐step partial melting model can explain it.     

A petrologic study of the IAB iron meteorites: Constraints on the formation of the IAB‐Winonaite parent body

Abstract— We studied 26 IAB iron meteorites containing silicate‐bearing inclusions to better constrain the many diverse hypotheses for the formation of this complex group. These meteorites contain inclusions that fall broadly into five types: (1) sulfide‐rich, composed primarily of troilite and containing abundant embedded silicates; (2) nonchondritic, silicate‐rich, comprised of basaltic, troctolitic, and peridotitic mineralogies; (3) angular, chondritic silicate‐rich, the most common type, with approximately chondritic mineralogy and most closely resembling the winonaites in composition and texture; (4) rounded, often graphite‐rich assemblages that sometimes contain silicates; and (5) phosphate‐bearing inclusions with phosphates generally found in contact with the metallic host. Similarities in mineralogy and mineral and O‐isotopic compositions suggest that IAB iron and winonaite meteorites are from the same parent body. We propose a hypothesis for the origin of IAB iron meteorites that combines some aspects of previous formation models for these meteorites. We suggest that the precursor parent body was chondritic, although unlike any known chondrite group. Metamorphism, partial melting, and incomplete differentiation (i.e., incomplete separation of melt from residue) produced metallic, sulfide‐rich and silicate partial melts (portions of which may have crystallized prior to the mixing event), as well as metamorphosed chondritic materials and residues. Catastrophic impact breakup and reassembly of the debris while near the peak temperature mixed materials from various depths into the re‐accreted parent body. Thus, molten metal from depth was mixed with near‐surface silicate rock, resulting in the formation of silicate‐rich IAB iron and winonaite meteorites. Results of smoothed particle hydrodynamic model calculations support the feasibility of such a mixing mechanism. Not all of the metal melt bodies were mixed with silicate materials during this impact and reaccretion event, and these are now represented by silicate‐free IAB iron meteorites. Ages of silicate inclusions and winonaites of 4.40‐4.54 Ga indicate this entire process occurred early in solar system history.     

The Miller Range 090340 and 090206 meteorites: Identification of new brachinite‐like achondrites with implications for the diversity and petrogenesis of the brachinite clan

Miller Range (MIL) 090340 and MIL 090206 are olivine‐rich achondrites originally classified as ureilites. We investigate their petrography, mineral compositions, olivine Cr valences, equilibration temperatures, and (for MIL 090340) oxygen isotope compositions, and compare them with ureilites and other olivine‐rich achondrites. We conclude that they are brachinite‐like achondrites that provide new insights into the petrogenesis of brachinite clan meteorites. MIL 090340,6 has a granoblastic texture and consists of ~97 modal % by area olivine (Fo = molar Mg/[Mg+Fe] = 71.3 ± 0.6). It also contains minor to trace augite, chromite, chlorapatite, orthopyroxene, metal, troilite, and terrestrial Fe‐oxides. Approximately 80% by area of MIL 090206,5 has a granoblastic texture of olivine (Fo 72.3 ± 0.1) plus minor augite and chromite, similar to MIL 090340 but also containing minor plagioclase. The rest of the section consists of a single crystal of orthopyroxene (~11 × 3 mm), poikilitically enclosing rounded grains of olivine (Fo = 76.1 ± 0.6), augite, chromite, metal, and sulfide. Equilibration temperatures for MIL 090340 and MIL 090206, calculated from olivine‐spinel, olivine‐augite, and two‐pyroxene thermometry range from ~800 to 930 °C. In both samples, symplectic intergrowths of Ca‐poor orthopyroxene + opaque phases (Fe‐oxides, sulfide, metal) occur as rims on and veins/patches within olivine. Before terrestrial weathering, the opaques were probably mostly sulfide, with minor metal. All petrologic properties of MIL 090340 and MIL 090206 are consistent with those of brachinite clan meteorites, and largely distinct from those of ureilites. Oxygen isotope compositions of olivine in MIL 090340 (δ¹⁸O = 5.08 ± 0.30‰, δ¹⁷O = 2.44 ± 0.21‰, and Δ¹⁷O = ?0.20 ± 0.12‰) are also within the range of brachinite clan meteorites, and well distinguished from ureilites. Olivine Cr valences in MIL 090340 and the granoblastic area of MIL 090206 are 2.57 ± 0.06 and 2.59 ± 0.07, respectively, similar to those of three brachinites also analyzed here (Brachina, Hughes 026, Nova 003). They are higher than those of olivine in ureilites, even those containing chromite. The valence systematics of MIL 090340, MIL 090206, and the three analyzed brachinites (lower Fo = more oxidized Cr) are consistent with previous evidence that brachinite‐like parent bodies were inherently more oxidized than the ureilite parent body. The symplectic orthopyroxene + sulfide/metal assemblages in MIL 090340, MIL 090206, and many brachinite clan meteorites have superficial similarities to characteristic “reduction rims” in ureilites. However, they differ significantly in detail. They likely formed by reaction of olivine with S‐rich fluids, with only minor reduction. MIL 090340 and the granoblastic area of MIL 090206 are similar in modal mineralogy and texture to most brachinites, but have higher Fo values typical of brachinite‐like achondrites. The poikilitic pyroxene area of MIL 090206 is more typical of brachinite‐like achondrites. The majority of their properties suggest that MIL 090340 and MIL 090206 are residues of low‐degree partial melting. The poikilitic area of MIL 090206 could be a result of limited melt migration, with trapping and recrystallization of a small volume of melt in the residual matrix. These two samples are so similar in mineral compositions, Cr valence, and cosmic ray exposure ages that they could be derived from the same lithologic unit on a common parent body.     

Geochemistry of 4 Vesta based on HED meteorites: Prospective study for interpretation of gamma ray and neutron spectra for the Dawn mission

Abstract— Asteroid 4 Vesta, believed to be the parent body of the howardite, eucrite, and diogenite (HED) meteorites, will be investigated by the Dawn orbiting spacecraft. Dawn carries a gamma ray and neutron detector (GRaND) that will measure and map some major‐ and trace‐element abundances. Drawing on HED geochemistry, we propose a mixing model that uses element ratios appropriate for the interpretation of GRaND data. Because the spatial resolution of GRaND is relatively coarse, the analyzed chemical compositions on the surface of Vesta will likely reflect mixing of three endmember components: diogenite, cumulate eucrite, and basaltic eucrite. Reliability of the mixing model is statistically investigated based on published whole‐rock data for HED meteorites. We demonstrate that the mixing model can accurately estimate the abundances of all the GRaND‐analyzed major elements, as well as of minor elements (Na, Cr, and Mn) not analyzed by this instrument. We also show how a similar mixing model can determine the modal abundance of olivine, and we compare estimated and normative olivine data for olivine‐bearing diogenites. By linking the compositions of well‐analyzed HED meteorites with elemental mapping data from GRaND, this study may help constrain the geological context for HED meteorites and provide new insight into the magmatic evolution of Vesta.     

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.     

The origin of eucrites,diogenites, and olivine diogenites: Magma ocean crystallization and shallow magma chamber processes on Vesta

The asteroid 4 Vesta is one of the very few heavenly bodies to have been linked to samples on Earth: the howardite‐eucrite‐diogenite (HED) meteorite suite. This large and diverse suite of meteorites provides a detailed picture of Vesta's igneous and postigneous history. We have used the range of igneous rock types and compositions in the HED suite to test a series of chemical models for solidification processes following peak melting (magma ocean) conditions on Vesta. Fractional crystallization cannot have been a dominant early process in the magma ocean because it leads to excessive Fe‐enrichment in the melt. Models that are dominated by equilibrium crystallization cannot produce orthopyroxene cumulates (diogenites). Our best models invoke 60–70% equilibrium crystallization of a magma ocean followed by continuous extraction of the residual melt into shallow magma chambers. Fractional crystallization in these magma chambers combined with continuous or periodic addition of more melt from the slowly compacting crystal mush (magmatic recharge) can produce all of the igneous HED lithologies (noncumulate and cumulate eucrites, diogenites, dunites, harzburgites, and olivine diogenites). Magmatic recharge can also explain the narrow range in eucrite compositions and the variability of incompatible trace element concentrations in diogenites. We predict an internal structure for Vesta that permits excavation of the HEDs during the formation of the Rheasilvia basin, while remaining consistent with observations from the Dawn mission and most impact models.