MgAl2O4 spinels from Allende and NWA 763 carbonaceous chondrites: Structural refinement,cooling history,and trace element contents

MgAl₂O₄ spinels from Allende and NWA 763 carbonaceous chondrites were studied by X‐ray single crystal diffraction, SEM, electron microprobe, LA‐ICP‐MS, and Raman spectroscopy. Those from Allende are almost pure, but, in one case, we found a strong FeO_tot zonation. Spinels from NWA 763 show Mg‐Fe²⁺ substitutions. Almost pure MgAl₂O₄ spinels from both meteorites underwent slow cooling and reached their intracrystalline closure temperature (T_c) in the range 460–520 °C. The NWA 763 spinel with higher FeO content shows a T_c of about 720 °C. X‐ray single crystal diffraction and Raman spectroscopy suggest a slow cooling and an ordered structure with trivalent cations in M site and divalent in T site. Among the trace elements, Ti and Co are enriched with respect to the terrestrial analogs, while Mn, Ni, and Sn show intermediate values between different terrestrial occurrences. Vanadium cannot be used as a tracer of extraterrestrial origin as for Cr‐spinels, because its content is similar in extraterrestrial and terrestrial spinels. In the zoned crystal from Allende, Co show a strong zonation similar to that of FeO.     

Tissemouminites: A new group of primitive achondrites spanning the transition between acapulcoites and winonaites

The Northwest Africa (NWA) 090 meteorite, initially classified as an acapulcoite, presents petrological, chemical, and isotopic characteristics comparable to a group of seven primitive winonaites: Dhofar 1222, NWA 725, NWA 1052, NWA 1054, NWA 1058, NWA 1463, and NWA 8614. Five of these samples were previously classified as acapulcoites or ungrouped achondrites before being reclassified as winonaites based on their oxygen isotopic compositions. These misclassifications are indicative of the particular compositional nature of these primitive achondrites. All contain relict chondrules and a lower closure temperature of metamorphism of 820 ± 20 °C compared to other typical winonaites, as well as mineral elemental compositions similar to those of acapulcoites. The oxygen isotopic signature of these samples, δ¹⁷O of 1.18 ± 0.17‰, δ¹⁸O of 3.18 ± 0.30‰, and Δ¹⁷O of −0.47 ± 0.02, is in fact resolvable from both acapulcoites and winonaites. We investigate the relationship between these eight primitive achondrites, typical winonaites, and acapulcoites, to redefine petrological, mineralogical, and geochemical criteria of primitive achondrite classification. Distinguishing between winonaites, acapulcoites, and this group of eight primitive achondrites can be unambiguously done using a combination of several mineralogical and chemical criteria. A combination of olivine fayalite content and FeO/MnO ratio, as well as plagioclase potassium content allow us to separate these three groups without the absolute necessity of oxygen isotope analyses. NWA 090 as well as the other seven primitive achondrites, although related to winonaites, are most likely derived from a parent body distinct from winonaites and acapulcoites–lodranites, and define a new group of primitive achondrites that can be referred to as tissemouminites.     

Petrology and oxygen isotopic compositions of calcium‐aluminum‐rich inclusions in primitive CO3.0‐3.1 chondrites

The petrologic and oxygen isotopic characteristics of calcium‐aluminum‐rich inclusions (CAIs) in CO chondrites were further constrained by studying CAIs from six primitive CO3.0‐3.1 chondrites, including two Antarctic meteorites (DOM 08006 and MIL 090010), three hot desert meteorites (NWA 10493, NWA 10498, and NWA 7892), and the Colony meteorite. The CAIs can be divided into hibonite‐bearing inclusions (spinel‐hibonite spherules, monomineralic grains, hibonite‐pyroxene microspherules, and irregular/nodular objects), grossite‐bearing inclusions (monomineralic grains, grossite‐melilite microspherules, and irregular/nodular objects), melilite‐rich inclusions (fluffy Type A, compact type A, monomineralic grains, and igneous fragments), spinel‐pyroxene inclusions (fluffy objects resembling fine‐grained spinel‐rich inclusions in CV chondrites and nodular/banded objects resembling those in CM chondrites), and pyroxene‐anorthite inclusions. They are typically small (98.4 ± 54.4 µm, 1SD) and comprise 1.54 ± 0.43 (1SD) area% of the host chondrites. Melilite in the hot desert and Colony meteorites was extensively replaced by a hydrated Ca‐Al‐silicate during terrestrial weathering and converted melilite‐rich inclusions into spinel‐pyroxene inclusions. The CAI populations of the weathered COs are very similar to those in CM chondrites, suggesting that complete replacement of melilite by terrestrial weathering, and possibly parent body aqueous alteration, would make the CO CAIs CM‐like, supporting the hypothesis that CO and CM chondrites derive from similar nebular materials. Within the CO3.0‐3.1 chondrites, asteroidal alteration significantly resets oxygen isotopic compositions of CAIs in CO3.1 chondrites (?¹⁷O: ?25 to ?2‰) but left those in CO3.0‐3.05 chondrites mostly unchanged (?¹⁷O: ?25 to ?20‰), further supporting the model whereby thermal metamorphism became evident in CO chondrites of petrologic type ≥3.1. The resistance of CAI minerals to oxygen isotope exchange during thermal metamorphism follows in the order: melilite + grossite < hibonite + anorthite < spinel + diopside + forsterite. Meanwhile, terrestrial weathering destroys melilite without changing the chemical and isotopic compositions of melilite and other CAI minerals.     

Spinels and oxygen fugacity in olivine‐phyric and lherzolitic shergottites

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

In search of the Earth‐forming reservoir: Mineralogical,chemical, and isotopic characterizations of the ungrouped achondrite NWA 5363/NWA 5400 and selected chondrites

High‐precision isotope data of meteorites show that the long‐standing notion of a “chondritic uniform reservoir” is not always applicable for describing the isotopic composition of the bulk Earth and other planetary bodies. To mitigate the effects of this “isotopic crisis” and to better understand the genetic relations of meteorites and the Earth‐forming reservoir, we performed a comprehensive petrographic, elemental, and multi‐isotopic (O, Ca, Ti, Cr, Ni, Mo, Ru, and W) study of the ungrouped achondrites NWA 5363 and NWA 5400, for both of which terrestrial O isotope signatures were previously reported. Also, we obtained isotope data for the chondrites Pillistfer (EL6), Allegan (H6), and Allende (CV3), and compiled available anomaly data for undifferentiated and differentiated meteorites. The chemical compositions of NWA 5363 and NWA 5400 are strikingly similar, except for fluid mobile elements tracing desert weathering. We show that NWA 5363 and NWA 5400 are paired samples from a primitive achondrite parent‐body and interpret these rocks as restite assemblages after silicate melt extraction and siderophile element addition. Hafnium‐tungsten chronology yields a model age of 2.2 ± 0.8 Myr after CAI, which probably dates both of these events within uncertainty. We confirm the terrestrial O isotope signature of NWA 5363/NWA 5400; however, the discovery of nucleosynthetic anomalies in Ca, Ti, Cr, Mo, and Ru reveals that the NWA5363/NWA 5400 parent‐body is not the “missing link” that could explain the composition of the Earth by the mixing of known meteorites. Until this “missing link” or a direct sample of the terrestrial reservoir is identified, guidelines are provided of how to use chondrites for estimating the isotopic composition of the bulk Earth.     

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.     

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.     

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.     

The Northwest Africa (NWA) 5790 meteorite: A mesostasis‐rich nakhlite with little or no Martian aqueous alteration

Northwest Africa (NWA) 5790 is the most recently discovered member of the nakhlite group. Its mineralogy differs from the other nakhlites with a high abundance mesostasis (38.1 ± 3.6 vol%) and scarcity of olivine (4.0 ± 2.2 vol%). Furthermore, zoning of augite phenocrysts, and other petrographic and chemical characteristics suggest that NWA 5790 samples the chilled margin of its parent lava flow/sill. NWA 5790 contains calcite and rare clay minerals that are evidence for its exposure to liquid water. The calcite forms a cement to coatings of dust on the outer surface of the find and extends into the interior of the meteorite within veins. The presence of microbial remains within the coating confirms that the dust and its carbonate cement are terrestrial in origin, consistent with the carbon and oxygen isotope composition of the calcite. The clay minerals are finely crystalline and comprise ~0.003 vol% of the meteorite. δD values of the clay minerals range from ?212 ± 109‰ to ?96 ± 132‰, and cannot be used to distinguish between a terrestrial or Martian origin. As petrographic results are also not definitive, we conclude that secondary minerals produced by Martian groundwaters are at best very rare within NWA 5790. The meteorite has therefore sampled a region of the lava flow/sill with little or no exposure to the aqueous solutions that altered other nakhlites. This isolation could relate to the scarcity of olivine in NWA 5790 because dissolution of olivine in other nakhlites by Martian groundwaters enhanced their porosity and permeability, and provided solutes for secondary minerals.     

Northwest Africa 773: Lunar origin and iron‐enrichment trend

Abstract— The meteorite Northwest Africa 773 (NWA 773) is a lunar sample with implications for the evolution of mafic magmas on the moon. A combination of key parameters including whole‐rock oxygen isotopic composition, Fe/Mn ratios in mafic silicates, noble gas concentrations, a KREEP‐like rare earth element pattern, and the presence of regolith agglutinate fragments indicate a lunar origin for NWA 773. Partial maskelynitization of feldspar and occasional twinning of pyroxene are attributed to shock deformation. Terrestrial weathering has caused fracturing and precipitation of Carich carbonates and sulfates in the fractures, but lunar minerals appear fresh and unoxidized. The meteorite is composed of two distinct lithologies: a two‐pyroxene olivine gabbro with cumulate texture, and a polymict, fragmental regolith breccia. The olivine gabbro is dominated by cumulate olivine with pigeonite, augite, and interstitial plagioclase feldspar. The breccia consists of several types of clasts but is dominated by clasts from the gabbro and more FeO‐rich derivatives. Variations in clast mineral assemblage and pyroxene Mg/(Mg + Fe) and Ti/(Ti + Cr) record an igneous Fe‐enrichment trend that culminated in crystallization of fayalite + silica + hedenbergite‐bearing symplectites. The Fe‐enrichment trend and cumulate textures observed in NWA 773 are similar to features of terrestrial ponded lava flows and shallow‐level mafic intrusives, indicating that NWA 773 may be from a layered mafic intrusion or a thick, differentiated lava flow. NWA 773 and several other mafic lunar meteorites have LREE‐enriched patters distinct from Apollo and Luna mare basalts, which tend to be LREE‐depleted. This is somewhat surprising in light of remote sensing data that indicates that the Apollo and Luna missions sampled a portion of the moon that was enriched in incompatible heatproducing elements.     

Constraints on the water,chlorine, and fluorine content of the Martian mantle

Previous estimates of the volatile contents of Martian basalts, and hence their source regions, ranged from nearly volatile‐free through estimates similar to those found in terrestrial subduction zones. Here, we use the bulk chemistry of Martian meteorites, along with Martian apatite and amphibole chemistry, to constrain the volatile contents of the Martian interior. Our estimates show that the volatile content of the source region for the Martian meteorites is similar to the terrestrial Mid‐Ocean‐Ridge Mantle source. Chlorine is enriched compared with the depleted terrestrial mantle but is similar to the terrestrial enriched source region; fluorine is similar to the terrestrial primitive mantle; and water is consistent with the terrestrial mantle. Our results show that Martian magmas were not volatile saturated; had water/chlorine and water/fluorine ratios ~0.4–18; and are most similar, in terms of volatiles, to terrestrial MORBs. Presumably, there are variations in volatile content in the Martian interior as suggested by apatite compositions, but more bulk chemical data, especially for fluorine and water, are required to investigate these variations. Finally, the Noachian Martian interior, as exemplified by surface basalts and NWA 7034, may have had higher volatile contents.     

Identification of a meteoritic component using chromium isotopic composition of impact rocks from the Lonar impact structure,India

The existence of mass‐independent chromium isotope variability of nucleosynthetic origin in meteorites and their components provides a means to investigate potential genetic relationship between meteorites and planetary bodies. Moreover, chromium abundances are depleted in most surficial terrestrial rocks relative to chondrites such that Cr isotopes are a powerful tool to detect the contribution of various types of extra‐terrestrial material in terrestrial impactites. This approach can thus be used to constrain the nature of the bolide resulting in breccia and melt rocks in terrestrial impact structures. Here, we report the Cr isotope composition of impact rocks from the ~0.57 Ma Lonar crater (India), which is the best‐preserved impact structure excavated in basaltic target rocks. Results confirm the presence of a chondritic component in several bulk rock samples of up to 3%. The impactor that created the Lonar crater had a composition that was most likely similar to that of carbonaceous chondrites, possibly a CM‐type chondrite.     

40Ar‐39Ar age determinations of lunar basalt meteorites Asuka 881757, Yamato 793169, Miller Range 05035, La Paz Icefield 02205, Northwest Africa 479, and basaltic breccia Elephant Moraine 96008

Abstract— ⁴⁰Ar‐³⁹Ar data are presented for the unbrecciated lunar basaltic meteorites Asuka (A‐) 881757, Yamato (Y‐) 793169, Miller Range (MIL) 05035, LaPaz Icefield (LAP) 02205, Northwest Africa (NWA) 479 (paired with NWA 032), and basaltic fragmental breccia Elephant Moraine (EET) 96008. Stepped heating ⁴⁰Ar‐³⁹Ar analyses of several bulk fragments of related meteorites A‐881757, Y‐793169 and MIL 05035 give crystallization ages of 3.763 ± 0.046 Ga, 3.811 ± 0.098 Ga and 3.845 ± 0.014 Ga, which are comparable with previous age determinations by Sm‐Nd, U‐Pb Th‐Pb, Pb‐Pb, and Rb‐Sr methods. These three meteorites differ in the degree of secondary ⁴⁰Ar loss with Y‐793169 showing relatively high Ar loss probably during an impact event ?200 Ma ago, lower Ar loss in MIL 05035 and no loss in A‐881757. Bulk and impact melt glass‐bearing samples of LAP 02205 gave similar ages (2.985 ± 0.016 Ga and 2.874 ± 0.056 Ga) and are consistent with ages previously determined using other isotope pairs. The basaltic portion of EET 96008 gives an age of 2.650 ± 0.086 Ga which is considered to be the crystallization age of the basalt in this meteorite. The Ar release for fragmental basaltic breccia EET 96008 shows evidence of an impact event at 631 ± 20 Ma. The crystallization age of 2.721 ± 0.040 Ga determined for NWA 479 is indistinguishable from the weighted mean age obtained from three samples of NWA 032 supporting the proposal that these meteorites are paired. The similarity of ⁴⁰Ar‐³⁹Ar ages with ages determined by other isotopic systems for multiple meteorites suggests that the K‐Ar isotopic system is robust for meteorites that have experienced a significant shock event and not a prolonged heating regime.     

The Northwest Africa 1500 meteorite: Not a ureilite,maybe a brachinite

Abstract– The Northwest Africa (NWA) 1500 meteorite is an olivine‐rich achondrite containing approximately 2–3 vol% augite, 1–2 vol% plagioclase, 1 vol% chromite, and minor orthopyroxene, Cl‐apatite, metal and sulfide. It was originally classified as a ureilite, but is currently ungrouped. We re‐examined the oxygen three‐isotope composition of NWA 1500. Results of ultra‐high precision (～0.03‰ for Δ¹⁷O) laser fluorination analyses of two bulk chips, and high precision (～0.3‰) secondary ion mass spectrometry (SIMS) analyses of olivine and plagioclase in a thin section, show that the oxygen isotope composition of NWA 1500 (Δ¹⁷O = ?0.22‰ from bulk samples and ?0.18 ± 0.06‰ from 16 mineral analyses) is within the range of brachinites. We compare petrologic and geochemical characteristics of NWA 1500 with those of brachinites and other olivine‐rich primitive achondrites, including new petrographic, mineral compositional and bulk compositional data for brachinites Hughes 026, Reid 013, NWA 5191, NWA 595, and Brachina. Modal mineral abundances, texture, olivine and pyroxene major and minor element compositions, plagioclase major element compositions, rare earth element abundances, and siderophile element abundances of NWA 1500 are within the range of those in brachinites and, in most cases, well distinguished from those of winonaites/IAB silicates, acapulcoites/lodranites, ureilites, and Divnoe. NWA 1500 shows evidence of internal reduction, in the form of reversely zoned olivine (Fo ～65–73 core to rim) and fine‐grained intergrowths of orthopyroxene + metal along olivine grain margins. The latter also occur in Reid 013, Hughes 026, NWA 5191, and NWA 595. We argue that reduction (olivine→enstatite + Fe⁰ + O₂) is the best hypothesis for their origin in these samples as well. We suggest that NWA 1500 should be classified as a brachinite, which has implications for the petrogenesis of brachinites. Fe‐Mn‐Mg compositions of brachinite olivine provide evidence of redox processes among bulk samples. NWA 1500 provides evidence for redox processes on a smaller scale as well, which supports the interpretation that these processes occurred in a parent body setting. SIMS data for ²⁶Al‐²⁶Mg isotopes in plagioclase in NWA 1500 show no ²⁶Mg excesses beyond analytical uncertainties (1–2‰). The calculated upper limit for the initial ²⁶Al/²⁷Al ratio of the plagioclase corresponds to an age younger than 7 Ma after CAI. Compared to ⁵³Mn‐⁵³Cr data for Brachina ( Wadhwa et al. 1998b ), this implies either a much younger formation age or a more protracted cooling history. However, Brachina is atypical and this comparison may not extend to other brachinites.     

Hydrogen isotopic composition of the Martian mantle inferred from the newest Martian meteorite fall,Tissint

The hydrogen isotopic composition of planetary reservoirs can provide key constraints on the origin and history of water on planets. The sources of water and the hydrological evolution of Mars may be inferred from the hydrogen isotopic compositions of mineral phases in Martian meteorites, which are currently the only samples of Mars available for Earth‐based laboratory investigations. Previous studies have shown that δD values in minerals in the Martian meteorites span a large range of ?250 to +6000‰. The highest hydrogen isotope ratios likely represent a Martian atmospheric component: either interaction with a reservoir in equilibrium with the Martian atmosphere (such as crustal water), or direct incorporation of the Martian atmosphere due to shock processes. The lowest δD values may represent those of the Martian mantle, but it has also been suggested that these values may represent terrestrial contamination in Martian meteorites. Here we report the hydrogen isotopic compositions and water contents of a variety of phases (merrillites, maskelynites, olivines, and an olivine‐hosted melt inclusion) in Tissint, the latest Martian meteorite fall that was minimally exposed to the terrestrial environment. We compared traditional sample preparation techniques with anhydrous sample preparation methods, to evaluate their effects on hydrogen isotopes, and find that for severely shocked meteorites like Tissint, the traditional sample preparation techniques increase water content and alter the D/H ratios toward more terrestrial‐like values. In the anhydrously prepared Tissint sample, we see a large range of δD values, most likely resulting from a combination of processes including magmatic degassing, secondary alteration by crustal fluids, shock‐related fractionation, and implantation of Martian atmosphere. Based on these data, our best estimate of the δD value for the Martian depleted mantle is ?116 ± 94‰, which is the lowest value measured in a phase in the anhydrously prepared section of Tissint. This value is similar to that of the terrestrial upper mantle, suggesting that water on Mars and Earth was derived from similar sources. The water contents of phases in Tissint are highly variable, and have been affected by secondary processes. Considering the H₂O abundances reported here in the driest phases (most likely representing primary igneous compositions) and appropriate partition coefficients, we estimate the H₂O content of the Tissint parent magma to be ≤0.2 wt%.     

Extraterrestrial chromite in Middle Ordovician marine limestone at Kinnekulle,southern Sweden—Traces of a major asteroid breakup event

Abstract— The distribution of sediment‐dispersed extraterrestrial chromite grains and other Cr‐rich spinels (>63 μm) has been studied in Middle Ordovician Orthoceratite Limestone from two quarries at Kinnekulle, southern Sweden. In the Thorsberg quarry, an ?3.2 m thick sequence of beds previously shown to be rich in fossil meteorites is also rich in sediment‐dispersed extraterrestrial chromite grains. Typically, 1–3 grains are found per kilogram of limestone. In the nearby Hällekis quarry, the same beds show similarly high concentrations of extraterrestrial chromite grains, but in samples representing the 9 m downward continuation of the section exposed at this site, only 5 such grains were found in a total of 379 kg of limestone. The extraterrestrial (equilibrated ordinary chondritic) chromite grains can be readily distinguished by a homogeneous and characteristic major element chemistry, including 2.0–3.5 wt% TiO₂ and stable V₂O₃ concentrations close to 0.7 wt%. Terrestrial Cr‐rich spinels have a wide compositional range and co‐exist with extraterrestrial chromite in some beds. These grains may be derived, for example, from mafic dykes exposed and weathered at the sea floor. Considering lithologic and stratigraphic aspects variations in sedimentation rate cannot explain the dramatic increase in extraterrestrial chromite seen in the upper part of the composite section studied. Instead, the difference may be primarily related to an increase in the ancient flux of extraterrestrial matter to Earth in connection with the disruption of the L chondrite parent body in the asteroid belt at about this time. The coexistence in some beds of high concentrations of chondritic chromite and terrestrial Cr‐rich spinels, however, indicates that redistribution of heavy minerals on the sea floor, related to changes in sea level and sea‐floor erosion and currents, must also be considered.     

The extremely reduced silicate‐bearing iron meteorite Northwest Africa 6583: Implications on the variety of the impact melt rocks of the IAB‐complex parent body

Northwest Africa (NWA) 6583 is a silicate‐bearing iron meteorite with Ni = 18 wt%. The oxygen isotope composition of the silicates (?′¹⁷O = ?0.439 ‰) indicates a genetic link with the IAB‐complex. Other chemical, mineralogical, and textural features of NWA 6583 are consistent with classification as a new member of the IAB‐complex. However, some unique features, e.g., the low Au content (1.13 μg g^?1) and the extremely reducing conditions of formation (approximately ?3.5 ?IW), distinguish NWA 6583 from the known IAB‐complex irons and extend the properties of this group of meteorites. The chemical and textural features of NWA 6583 can be ascribed to a genesis by impact melting on a parent body of chondritic composition. This model is also consistent with one of the most recent models for the genesis of the IAB‐complex. Northwest Africa 6583 provides a further example of the wide lithological and mineralogical variety that impact melting could produce on the surface of a single asteroid, especially if characterized by an important compositional heterogeneity in space and time like a regolith.     

Northwest Africa 482: A crystalline impact‐melt breccia from the lunar highlands

Abstract— Northwest Africa 482 (NWA 482) is a crystalline impact‐melt breccia from the Moon with highlands affinities. The recrystallized matrix and the clast population are both highly anorthositic. Clasts are all related to the ferroan anorthosite suite, and include isolated plagioclase crystals and lithic anorthosites, troctolites, and spinel troctolites. Potassium‐, rare‐earth‐element‐, and phosphorus‐bearing (KREEP) and mare lithologies are both absent, constraining the source area of this meteorite to a highland terrain with little to no KREEP component, most likely on the far side of the Moon. Glass is present in shock veins cutting through the sample and in several large melt pockets, indicating a second impact event. There are two separate events recorded in the ⁴⁰Ar‐³⁹Ar system: one at ～3750 Ma, which completely reset the K‐Ar system, and one at ?2400 Ma, which caused only partial degassing. These events could represent, respectively, crystallization of the impact‐melt breccia and later formation of the glass, or the formation of the glass and a later thermal event. The terrestrial age of the meteorite is 8.6 ± 1.3 ka. This age corresponds well with the modest amount of weathering in the rock, in the form of secondary phyllosilicates and carbonates. Based on terrestrial age and location, lithology, and chemistry, NWA 482 is unique among known lunar meteorites.     

Petrological,petrofabric, and oxygen isotopic study of five ungrouped meteorites related to brachinites

Northwest Africa (NWA) 6112, Miller Range (MIL) 090206 (plus its pairs: MIL 090340 and MIL 090405), and Divnoe are olivine‐rich ungrouped achondrites. We investigated and compared their petrography, mineralogy, and olivine fabrics. We additionally measured the oxygen isotopic compositions of NWA 6112. They show similar petrography, mineralogy, and oxygen isotopic compositions and we concluded that these five meteorites are brachinite clan meteorites. We found that NWA 6112 and Divnoe had a c axis concentration pattern of olivine fabrics using electron backscattered diffraction (EBSD). NWA 6112 and Divnoe are suggested to have been exposed to magmatic melt flows during their crystallization on their parent body. On the other hand, the three MIL meteorites have b axis concentration patterns of olivine fabrics. This indicates that the three MIL meteorites may be cumulates where compaction of olivine grains was dominant. Alternatively, they formed as residues and were exposed to olivine compaction. The presence of two different olivine fabric patterns implies that the parent body(s) of brachinite clan meteorites experienced diverse igneous processes.     

Chlorine abundances in meteorites

Abstract— We used the nuclear reaction ³⁷Cl (n,γ) ³⁸Ar, achieved during neutron irradiation for dating meteorites by the ³⁹Ar‐⁴⁰Ar technique, to calculate the elemental Cl concentration of 132 samples of 94 different meteorites (mostly finds) representing several different classes. determined k and ca concentrations are also reported. Total [Cl] varies considerably, both among meteorites of the same class and among different meteorite classes. The range in [Cl] is approximately 15–177 ppm for ordinary chondrites; approximately 24–650 ppm for enstatite chondrites; approximately 4–177 ppm for eucrites; approximately 7–128 ppm for mesosiderites; approximately 35–268 ppm for acapulcoites and lodranites; and approximately 12–507 ppm for winonaites and iron silicates. As expected, most differentiated meteorites have lower [Cl] compared to chondrites and iron silicates. Analyses of 11 interior samples (～0.1 g each) of a large L6 chondrite varied over 68–129 ppm, which is a measure of the homogeneity of Cl distribution. By evaluating Ar release during stepwise sample degassing, we separated the Cl into low‐temperature and high‐temperature components, the former of which may consist of terrestrial contamination. Most samples show low‐temperature Cl concentrations of <40 ppm, but for several samples terrestrial Cl contamination constitutes significant fractions of the total Cl. Among most differentiated meteorites, finds show considerably greater low‐temperature [Cl] compared to falls.