Phyllosilicates in the matrix of the unique carbonaceous chondrite Lewis Cliff 85332 and possible implications for the aqueous alteration of CI chondrites

Abstract— The fine-grained matrix of the unique, unequilibrated carbonaceous chondrite Lewis Cliff (LEW) 85332 has been studied by scanning electron microscopy (SEM), electron probe microanalysis (EPMA) and transmission electron microscopy (TEM). Compositionally, LEW 85332 has a matrix that is more Fe-rich than typical CI chondrites but has elemental abundance ratios that appear to be closer to CI matrices than to CM or CR chondrites. The mineralogy of the matrix is dominated by phyllosilicate phases that are predominantly interlayered Fe-rich serpentine/saponite; anhydrous silicate phases such as olivine and pyroxene are rare. Minor magnetite, troilite and ferrihydrite also occur associated with the phyllosilicates. Despite the high degree of weathering in LEW 85332, the phyllosilicates appear to have an extraterrestrial origin, but the highly variable Mg/Fe ratios of saponite may be the result of partial terrestrial oxidation of Fe-rich saponite to a more Mg-rich saponite and ferrihydrite. Alternatively, some of the ferrihydrite may have formed as a result of terrestrial weathering of Fe-Ni metal. The compositional and mineralogical data suggest that the matrix of LEW 85332 may represent a very early stage in the type of aqueous alteration experienced by the CI chondrites, although it is improbable that LEW 85332 was a precursor to the CI chondrites because of its high abundance of chondrules. The absence of carbonates, the high-Fe content of the matrix and phyllosilicate phases and relatively low abundance of magnetite all indicate that the degree of oxidation and leaching of LEW 85332 matrix was significantly less than that experienced by the CI chondrites. The absence of clear evidence for alteration of chondrules suggests that either the formation of the hydrous phases in the matrix occurred prior to accretion or that alteration occurred on a parent body and involved limited amounts of fluid, such that the reactions took place preferentially and exclusively within the fine-grained (anhydrous?) matrix materials.     

Coolidge and Loongana 001: A new carbonaceous chondrite grouplet

Abstract— Petrographic and bulk compositional data suggest the existence of a new grouplet of carbonaceous chondrites consisting of Coolidge and Loongana 001. Coolidge is a carbonaceous chondrite find from Kansas, USA, previously considered a metamorphosed CV chondrite. Loongana 001 is a recent find from Western Australia. It has a high matrix/chondrule modal abundance ratio, 1–2 vol% refractory inclusions and high refractory lithophile abundance ratios (～1.35x CI), indicating that it is a carbonaceous chondrite. Coolidge and Loongana 001 have many compositional and petrographic similarities. They have refractory element abundances in the range of CV chondrites, significantly higher than those in the CR chondrites. They have similar volatile element abundance patterns showing low volatile element abundances relative to both CR and CV chondrites. Coolidge and Loongana 001 have similar chondrule dimensions and shapes, oxidation states and opaque mineral assemblages. They are also similar in petrologic type (3.8–4) and shock stage (S2). Although both Coolidge and Loongana 001 may be related to the CV clan, they are not CV chondrites, nor are they formed by metamorphism of a CV precursor. They are distinctly different in composition from CV chondrites and their chondrules are smaller and have a much lower abundance of coarse-grained chondrule rims. Coolidge and Loongana 001 constitute a distinct carbonaceous chondrite grouplet.     

Geochemistry of the ungrouped carbonaceous chondrite Tagish Lake,the anomalous CM chondrite Bells,and comparison with CI and CM chondrites

Abstract— I have determined the composition via instrumental neutron activation analysis of a bulk pristine sample of the Tagish Lake carbonaceous chondrite fall, along with bulk samples of the CI chondrite Orgueil and of several CM chondrites. Tagish Lake has a mean of refractory lithophile element/Cr ratios like those of CM chondrites, and distinctly higher than the CI chondrite mean. Tagish Lake exhibits abundances of the moderately volatile lithophile elements Na and K that are slightly higher than those of mean CM chondrites. Refractory through moderately volatile siderophile element abundances in Tagish Lake are like those of CM chondrites. Tagish Lake is distinct from CM chondrites in abundances of the most volatile elements. Mean CI‐normalized Se/Co, Zn/Co and Cs/Co for Tagish Lake are 0.68 ± 0.01, 0.71 ± 0.07 and 0.76 ± 0.02, while for all available CM chondrite determinations, these ratios lie between 0.31 and 0.61, between 0.32 and 0.58, and between 0.39 and 0.74, respectively. Considering petrography, and oxygen isotopic and elemental compositions, Tagish Lake is an ungrouped member of the carbonaceous chondrite clan. The overall abundance pattern is similar to those of CM chondrites, indicating that Tagish Lake and CMs experienced very similar nebular fractionations. Bells is a CM chondrite with unusual petrologic characteristics. Bells has a mean CI‐normalized refractory lithophile element/Cr ratio of 0.96, lower than for any other CM chondrite, but shows CI‐normalized moderately volatile lithophile element/Cr ratios within the ranges of other CM chondrites, except for Na which is low. Iridium, Co, Ni and Fe abundances are like those of CM chondrites, but the moderately volatile siderophile elements, Au, As and Sb, have abundances below the ranges for CM chondrites. Abundances of the moderately volatile elements Se and Zn of Bells are within the CM ranges. Bells is best classified as an anomalous CM chondrite.     

Infrared spectroscopic taxonomy for carbonaceous chondrites from speciation of hydrous components

Abstract— Mid‐infrared absorption spectra for all types of carbonaceous chondrites were obtained in this study to establish a versatile method for spectroscopic classification of carbonaceous chondrites. Infrared spectra were measured using a conventional KBr pellet method and diamond press method. Spectra of hydrous carbonaceous chondrites exhibit intense O‐H stretching vibrations. CI chondrites are identifiable by a characteristic sharp absorption band appearing at 3685 cm^?1, which is mainly attributable to serpentine. X‐ray diffraction analysis showed the presence of serpentine. However, Yamato (Y‐) 82162 (C1) does not have the band at 3685 cm^?1 because of its thermal metamorphism. CM and CR chondrites have an intense absorption band at approximately 3600 cm^?1. This absorption tends to appear in CM chondrites more strongly than CR chondrites because the intensity ratios of an OH stretching mode at 3520 cm^?1 compared to 3400 cm^?1 for CM chondrites are in the range of 0.95–1.04, which is systematically higher than those of CR chondrites (0.86–0.88). Therefore, the two types of chondrites are distinguishable by their respective infrared spectra. The spectrum feature of the Tagish Lake meteorite is attributable to neither CI nor CM chondrites. CO chondrites are characterized by weak and broad absorption at 3400 cm^?1. CV chondrites have weak or negligible absorption of water. CK chondrites also have no water‐induced absorption. CH and CB chondrites have a sharp absorption at 3692 cm^?1 indicating the presence of chrysotile, which is also supported by observations of X‐ray diffraction and TEM. The combination of spectroscopic classification and the diamond press method allows classification of carbonaceous chondrites of very valuable samples with small quantities. As one example, carbonaceous chondrite clasts in brecciated meteorites were classified using our technique. Infrared spectra for a fragment of carbonaceous clasts (<1 μg) separated from Willard (b) and Tsukuba were measured. The 3685 cm^?1 band found in CI chondrites was clearly detected in the clasts, indicating that they are CI‐like clasts.     

A study of presolar material in hydrated lithic clasts from metal-rich carbonaceous chondrites

We report on the investigation of presolar grain inventories of hydrated lithic clasts in three metal-rich carbonaceous chondrites from the CR clan, Acfer 182 (CH3), Isheyevo (CH3/CB_b3), and Lewis Cliff (LEW) 85332 (C3-un), as well as the carbon- and nitrogen-isotopic compositions of the fine-grained clast material. Eleven presolar silicate grains as well as nine presolar silicon carbide (SiC) grains were identified in the clasts. Presolar silicate abundances range from 4 to 22 parts per million (ppm), significantly lower than in pristine meteorites and interplanetary dust particles (IDP), and comparable to recent findings for CM2s and CR2 interchondrule matrix. SiC concentrations lie between 9 and 23 ppm, and are comparable to the values for CI, CM, and CR chondrites. The results of our investigation suggest similar alteration pathways for the clast material, the interchondrule matrix of the CR2 chondrites, and the fine-grained fraction of CM2 chondrites. Fine-grained matter of all three meteorites contains moderate to high ¹⁵N-enrichments (~50‰ ≤ δ¹⁵N ≤ ~1600‰) compared to the terrestrial value, indicating the presence of primitive organic material. We observed no correlation between ¹⁵N-enrichments and presolar dust concentrations in the clasts. This is in contrast to the findings from a suite of primitive IDPs, which display in several cases enhanced bulk ¹⁵N/¹⁴N ratios and high presolar grain abundances of several hundred or even thousand ppm. The bulk ¹⁵N/¹⁴N ratios of the clasts are comparable to the range for primitive IDPs, suggesting a nitrogen carrier less susceptible to destruction by aqueous alteration than silicate stardust.     

Mineralogy,petrology and geochemistry of carbonaceous chondritic clasts in the LEW 85300 polymict eucrite

Abstract— We have performed a detailed petrologic and mineralogic study of two chondritic clasts from the polymict eucrite Lewis Cliff (LEW) 85300, and performed chemical analyses by INAA and RNAA on one of these. Petrologically, the clasts are identical and are composed of dispersed aggregates, chondrules and chondrule fragments supported by matrix. The aggregates and chondrules are composed of olivine (Fo_100–45), orthopyroxene (Wo_1–2En_98–60), plus some diopside. The matrix consists of fine-grained olivine (Fo_60–53), and lesser orthopyroxene and augite. Fine-grained saponite is common in the matrix. The bulk major element composition of the matrix is identical in both clasts and similar to that of CM, CO and CV chondrites. The bulk composition of the clast studied by INAA and RNAA shows unusual abundance patterns for lithophile, siderophile and chalcophile elements but is basically chondritic. The INAA/RNAA data preclude assignment of the LEW 85300,15 clast to any commonly accepted group of carbonaceous chondrite. The unusual rare earth element abundance pattern may, in part, be due to terrestrial alteration.     

THE ATLANTA ENSTATITE CHONDRITE BRECCIA

Atlanta is the fifth known brecciated enstatite chondrite. It contains a centimeter-sized troilite-rich clast, similar to those that occur in Blithfield. All of these clasts probably formed in the solar nebula under high pS₂/pO₂ conditions in a gas of non-cosmic composition. The absence of ordinary or carbonaceous chondrite clasts in any of the enstatite chondrite breccias and absence of enstatite chondrite clasts or materials formed at high pS₂/pO₂ ratios in ordinary and carbonaceous chondrite breccias support the model that enstatite chondrites were formed at a location distant from those of the other chondritic groups.     

Carbonaceous chondrite clasts in the howardites Bholghati and EET87513

Abstract— Twenty-two carbonaceous chondrite clasts from the two howardites Bholghati and EET87513 were analyzed. Clast N from EET87513 is a fragment classified as CM2 material on the basis of texture, bulk composition, mineralogy, and bulk O isotopic composition. Carbonaceous chondrite clasts from Bholghati, for which less data are available because of their small size, can be divided into two petrologic types: C1 and C2. C1 clasts are composed of opaque matrix with rare coarse-grained silicates as individual mineral fragments; textures resemble CI meteorites and some dark inclusions from CR meteorites. Opaque matrix is predominantly composed of flaky saponite; unlike typical CI and CR meteorites, serpentine is absent in the samples we analyzed. C2 clasts contain chondrules, aggregates, and individual fragments of coarse-grained silicates in an opaque matrix principally composed of saponite and anhydrous ferromagnesian silicates with flaky textures similar to phyllosilicates. These anhydrous ferromagnesian silicates are interpreted as the product of heating of pre-existing serpentine. The carbonaceous chondrite clasts we have studied from these two howardites are, with one notable exception (clast N from EET87513), mineralogically distinct from typical carbonaceous chondrites. However, these clasts have very close affinities to carbonaceous chondrites and have also experienced thermal metamorphism and aqueous alteration, but to different degrees.     

Mineralogy and chemistry of Rumuruti: The first meteorite fall of the new R chondrite group

Abstract— The Rumuruti meteorite shower fell in Rumuruti, Kenya, on 1934 January 28 at 10:43 p.m. Rumuruti is an olivine-rich chondritic breccia with light-dark structure. Based on the coexistence of highly recrystallized fragments and unequilibrated components, Rumuruti is classified as a type 3–6 chondrite breccia. The most abundant phase of Rumuruti is olivine (mostly Fa_～39) with about 70 vol%. Feldspar (～14 vol%; mainly plagioclase), Ca-pyroxene (5 vol%), pyrrhotite (4.4 vol%), and pentlandite (3.6 vol%) are major constituents. All other phases have abundances below 1 vol%, including low-Ca pyroxene, chrome spinels, phosphates (chlorapatite and whitlockite), chalcopyrite, ilmenite, tridymite, Ni-rich and Ge-containing metals, kamacite, and various particles enriched in noble metals like Pt, Ir, arid Au. The chemical composition of Rumuruti is chondritic. The depletion in refractory elements (Sc, REE, etc.) and the comparatively high Mn, Na, and K contents are characteristic of ordinary chondrites and distinguish Rumuruti from carbonaceous chondrites. However, S, Se, and Zn contents in Rumuruti are significantly above the level expected for ordinary chondrites. The oxygen isotope composition of Rumuruti is high in δ¹⁷O (5.52 ‰) and δ¹⁸O (5.07 ‰). Previously, a small number of chondritic meteorites with strong similarities to Rumuruti were described. They were called Carlisle Lakes-type chondrites and they comprise: Carlisle Lakes, ALH85151, Y-75302, Y-793575, Y-82002, Acfer 217, PCA91002, and PCA91241, as well as clasts in the Weatherford chondrite. All these meteorites are finds from hot and cold deserts having experienced various degrees of weathering. With Rumuruti, the first meteorite fall has been recognized that preserves the primary mineralogical and chemical characteristics of a new group of meteorites. Comparing all chondrites, the characteristic features can be summarized as follows: (a) basically chondritic chemistry with ordinary chondrite element patterns of refractory and moderately volatile lithophiles but higher abundances of S, Se, and Zn; (b) high degree of oxidation (37–41 mol% Fa in olivine, only traces of Fe, Ni-metals, occurrence of chalcopyrite); (c) exceptionally high Δ¹⁷O values of about 2.7 for bulk samples; (d) high modal abundance of olivine (～70 vol%); (e) Ti-Fe³⁺?rich chromite (～5.5 wt% TiO₂); (f) occurrence of various noble metal-rich particles; (g) abundant chondritic breccias consisting of equilibrated clasts and unequilibrated lithologies. With Rumuruti, nine meteorite samples exist that are chemically and mineralogically very similar. These meteorites are attributed to at least eight different fall events. It is proposed in this paper to call this group R chondrites (rumurutiites) after the first and only fall among these meteorites. These meteorites have a close relationship to ordinary chondrites. However, they are more oxidized than any of the existing groups of ordinary chondrites. Small, but significant differences in chemical composition and in oxygen isotopes between R chondrites and ordinary chondrites exclude formation of R chondrites from ordinary chondrites by oxidation. This implies a separate, independent R chondrite parent body.     

Anorthite‐rich chondrules in CR and CH carbonaceous chondrites: Genetic link between calcium‐aluminum‐rich inclusions and ferromagnesian chondrules

Abstract— Anorthite‐rich chondrules in CR and CH carbonaceous chondrites consist of magnesian low‐Ca pyroxene and forsterite phenocrysts, FeNi‐metal nodules, interstitial anorthite, Al‐Ti‐Cr‐rich low‐Ca and high‐Ca pyroxenes, and crystalline mesostasis composed of silica, anorthite and high‐Ca pyroxene. Three anorthite‐rich chondrules contain relic calcium‐aluminum‐rich inclusions (CAIs) composed of anorthite, spinel, ±Al‐diopside, and ± forsterite. A few chondrules contain regions which are texturally and mineralogically similar to magnesian (type I) chondrules and consist of forsterite, low‐Ca pyroxene and abundant FeNi‐metal nodules. Anorthite‐rich chondrules in CR and CH chondrites are mineralogically similar to those in CV and CO carbonaceous chondrites, but contain no secondary nepheline, sodalite or ferrosilite. Relatively high abundances of moderately‐volatile elements such as Cr, Mn and Si in the anorthite‐rich chondrules suggest that these chondrules could not have been produced by volatilization of the ferromagnesian chondrule precursors or by melting of the refractory materials only. We infer instead that anorthite‐rich chondrules in carbonaceous chondrites formed by melting of the reduced chondrule precursors (olivine, pyroxenes, FeNi‐metal) mixed with the refractory materials, including relic CAIs, composed of anorthite, spinel, high‐Ca pyroxene and forsterite. The observed mineralogical and textural similarities of the anorthite‐rich chondrules in several carbonaceous chondrite groups (CV, CO, CH, CR) may indicate that these chondrules formed in the region(s) intermediate between the regions where CAIs and ferromagnesian chondrules originated. This may explain the relative enrichment of anorthite‐rich chondrules in ¹⁶O compared to typical ferromagnesian chondrules (Russell et al., 2000).     

The Ningqiang Meteorite: Classification and Petrology of an Anomalous CV Chondrite

Abstract— Ningqiang is an anomalous CV chondrite (oxidized subgroup) containing a high abundance of aggregational inclusions (13.7 vol.%) and low abundances of refractory inclusions (1.0^+1.0_–0.5 vol.%) and bulk refractory lithophiles (～0.82 × CV). Ningqiang may have agglomerated after most refractory inclusions at the nebular midplane had already been incorporated into other objects. Coarse-grained rims surround only ～5% of Ningqiang chondrules, compared to ～50% in normal CV chondrites. Aggregational inclusions appear to have formed by incipient melting of fine-grained aggregates at relatively low temperatures in the solar nebula, possibly by the mechanism responsible for chondrule formation. Granoblastic porphyritic chondrules, which contain olivines forming 120° triple junctures and no mesostasis, probably formed in the solar nebula by incomplete melting of precursor materials that were olivine normative and had relatively low concentrations of Si, Ca, Al, Fe and Na.     

From whom Bells tolls: Reclassifying Bells among CR chondrites and implications for the formation conditions of CR parent bodies

The ungrouped carbonaceous chondrite (CC) Bells has long been considered petrographically similar to CM chondrites based on its matrix abundance and degree of aqueous alteration, but also shows significant isotopic affinities to CR chondrites. Its taxonomic status is thus important for clarifying the relationship of the CRHB (formerly “CR”) clan with other CCs. In this study, we measured the oxygen isotopic compositions of olivines in type I chondrules and isolated olivine grains in Bells. Bells olivines mostly have ∆¹⁷O > −4‰, similar to CR chondrites but unlike other CCs that are rich in refractory inclusions, in which chondrules are generally richer in ¹⁶O. Therefore, Bells is a CR chondrite (albeit an anomalous one), most similar to the rare, matrix-rich CRs like Al Rais. These chondrites (i) may not necessarily derive from the same primary parent body as mainstream CRs, (ii) bear witness to significant variations of the matrix/chondrule ratio within the CRHB clan, and (iii) may be a good analog for samples retrieved by the space mission OSIRIS-REx.     

Are high‐temperature fractionations in the solar nebula preserved in highly siderophile element systematics of the Earth's mantle?

Abstract— The relative abundances of the highly siderophile elements (HSE) Os, Ir, Ru, Pt, Rh, and Pd in relatively pristine lherzolites differ from solar abundance ratios and are several orders of magnitude higher than predicted for equilibrium distribution between metal/silicate (core‐mantle). The samples are characterized by a mean Ca/Al ratio of 1.18 ± 0.09 σ_M and a mean Ca/Si ratio of 0.10 ± 0.01 σ_M, overlapping with a mean Ca/Al of 1.069 ± 0.044 σ_M and a mean Ca/Si of 0.081 ± 0.023 σ_M found in chondrites (Wasson and Kallemeyn 1988). Interestingly, the CI‐normalized abundance pattern shows decreasing solar system normalized abundances with increasing condensation temperatures. The abundance of the moderately volatile element Pd is about 2x higher than those in the most refractory siderophiles Ir and Os. Thus, the HSE systematics of upper mantle samples suggest that the late bombardment, which added these elements to the accreting Earth, more closely resembles materials of highly reduced EH or EL chondrites than carbonaceous chondrites. In fact, the HSE in the Earth mantle are even more fractionated than the enstatite chondrites—an indication that some inner solar system materials were more highly fractionated than the latter.     

Origin of dark clasts in the Acfer 059/El Djouf 001 CR2 chondrite

Abstract— The ten specimens of the paired Acfer 059/El Djouf 001 CR2 chondrite contain abundant lithic fragments which we refer to as dark clasts. Petrological and mineralogical studies reveal that they are not related to the CR2 host meteorite but are similar to dark clasts in other CR2 chondrites. Dark clasts consist of chondrule and mineral fragments, phyllosilicate fragments and clusters, magnetite, sulfides and accessory phases, embedded into a very fine-grained, phyllosilicate-rich matrix. Magnetite has morphologies known from CI chondrites: spherules, framboids and platelets. Average abundances of major elements in the dark clasts are mostly in the range of both CR and CV chondrites, but strong depletions in Na and S are apparent. Oxygen isotopic compositions of two dark clasts suggest relationships to type 3 carbonaceous chondrites and dark inclusions in Allende. The dark clasts are clearly different in texture and mineralogical composition from the host matrix of Acfer 059/El Djouf 001. Therefore, these dark clasts are xenoliths and are quite unlike the Acfer 059/El Djouf 001 CR2 host meteorite. We suggest that dark clasts accreted at the same time with all other components during the formation of Acfer 059/El Djouf 001 whole rock.     

Fe‐Mn systematics of type IIA chondrules in unequilibrated CO,CR, and ordinary chondrites

Abstract– We have examined Fe/Mn systematics of 34 type IIA chondrules in eight highly unequilibrated CO, CR, and ordinary chondrites using new data from this study and prior studies from our laboratory. Olivine grains from type IIA chondrules in CO chondrites and unequilibrated ordinary chondrites (UOC) have significantly different Fe/Mn ratios, with mean molar Fe/Mn = 99 and 44, respectively. Olivine analyses from both these chondrite groups show well‐defined trends in Mn versus Fe (afu) and molar Fe/Mn versus Fe/Mg diagrams. In general, type IIA chondrules in CR chondrites have properties intermediate between those in UOC and CO chondrites. In most UOC and CR type IIA chondrules, the Fe/Mn ratio of olivine decreases during crystallization, whereas in CO chondrites the Fe/Mn ratio does not appear to change. It is difficult to interpret the observed Fe/Mn trends in terms of differing moderately volatile element depletions inherited from precursor materials. Instead, we suggest that significant differences in the abundances of silicates and sulfides ± metals in the precursor material, as well as open‐system behavior during chondrule formation, were responsible for establishing the different Fe/Mn trends. Using Fe‐Mn‐Mg systematics, we are able to identify relict grains in type IIA chondrules, which could be derived from previous generations of chondrules, including chondrules from other chondrite groups, and possibly chondritic reservoirs that have not been sampled previously.     

Mineralogy of carbonaceous chondrite clasts in HED achondrites and the Moon

Abstract The majority of the carbonaceous chondrite clasts found in howardites, eucrites and diogenites are CM2 material, a lesser proportion is CR2 material, and other rare types are present. A single clast that was found on the Moon and called the Bench Crater meteorite is apparently shocked CM1 material. The CM2 clasts are matrix supported mixtures of olivine-pyroxene-phyllosilicate-sulfide bearing aggregates, loose olivines and pyroxenes, sulfides, carbonates, and sinuous spinel-phyllosilicate-diopside calcium-aluminum-rich inclusions (CAIs). Magnetite and metal are rare. Some aggregates have fine-grained rims of material resembling matrix. The opaque, fine-grained matrix consists predominantly of serpentine of extremely variable composition and sulfides; tochilinite is occasionally present. The trace element data for one Jodzie clast from this study and the average of similar clasts from Kapoeta support a CM classification; volatiles are depleted relative to CI and enriched relative to CR material. The CR2 clasts are found (in small numbers) in only four howardites: Bholghati, Jodzie, Kapoeta and Y793497. Petrographically, they are matrix-supported mixtures of olivine aggregates (sometimes containing sulfides), loose olivines, pyrrhotite, pentlandite, low-Ca pyroxene (minor), hedenbergite (rare), kamacite (rare and only found within olivine), Ca-carbonates and abundant magnetite framboids and plaquets. Phyllosilicates are fine-grained and largely confined to matrix; they are mixtures of serpentine and saponite. The matrix of CR2 clasts also contains pyrrhotite, pentlandite, chromite and a significant fraction of poorly-crystalline material with the same bulk composition as matrix phyllosilicate. There is evidence of heating in a substantial number of clasts, both CM2 and CR2, including: (1) corrugated serpentine flakes, (2) pseudomorphs of anhydrous ferromagnesian material after flaky phyllosilicates, and (3) hedenbergite rims on calcite. While the timing of the hedenbergite rims is debatable, the destruction of phyllosilicates clearly occurred at a late stage, plausibly during impact onto the HED asteroid(s) and Moon, and required peak heating temperatures on the order of 400 °C. We note that in general, CM2 material was the most common carbonaceous chondrite lithology impacting the HED asteroids (with howardites and eucrites taken together), as it is for the Earth today. A total of 61 out of 75 carbonaceous chondrite clasts from HED meteorites belong to the CM clan, petrologic grade 2. This is also supported by published siderophile and volatile element data on howardites, eucrites and diogenites that are taken to indicate that CM-like materials were the most common impactors on the HED asteroid(s). The ratio of CR/CM clasts in HED asteroids is essentially the same as for modern falls at Earth. This may indicate that the ratio of disaggregated CM2 to CR2 asteroidal material has been approximately constant through the history of the solar system. Finally, our results are also compatible with type-2 carbonaceous chondrites being equivalent to or from the same source as the material that originally accreted to form the HED asteroid.     

A new metal‐rich chondrite grouplet

Abstract— A new grouplet of primitive, metal‐rich chondrites, here called the CB (C, carbonaceous; B, bencubbinite) chondrites, has been recognized. It includes Bencubbin, Weatherford, Hammadah al Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627. Their mineral compositions, as well as their oxygen and nitrogen isotopic compositions, indicate that they are closely related to the CR and CH chondrites, all of which are members of the more inclusive CR clan. CB chondrites have much greater metal/silicate ratios than any other chondrite group, widely increasing the range of metal/silicate fractionation recorded in solar nebular processes. They also have the greatest moderately volatile lithophile element depletions of any chondritic materials. Metal has compositional trends and zoning patterns that suggest a primitive condensation origin, in contrast with metal from other chondrite groups. CB chondrites, as well as other CR clan chondrites, have much heavier nitrogen (higher ¹⁵N/¹⁴N) than that in other chondrite groups. The primitive characteristics of the CB chondrites suggest that they contain one of the best records of early nebular processes. Another chondrite, Grosvenor Mountains 95551, is petrographically similar to the CB chondrites, but its mineral and oxygen and nitrogen isotope compositions indicate that it formed from a different nebular reservoir.     

The Bencubbin chondrite breccia and its relationship to CR chondrites and the ALH85085 chondrite

Abstract— Bencubbin is an unclassified meteorite breccia which consists mainly of host silicate (～40 vol.%) and host metal (～60%) components. Rare (< 1%) ordinary chondrite clasts and a dark xenolith (formerly called a carbonaceous chondrite clast) are also found. A petrologic study of the host silicates shows that they have textures, modes, mineralogy and bulk compositions that are essentially the same as that of barred olivine (BO) chondrules, and they are considered to be BO chondritic material. Bulk compositions of individual host silicate clasts are identical and differ only in their textures which are a continuum from coarsely barred, to finely barred, to feathery microcrystalline; these result from differing cooling rates. The host silicates differ from average BO chondrules only in being angular clasts rather than fluid droplet-shaped objects, and in being larger in size (up to 1 cm) than most chondrules; but large angular to droplet-shaped chondrules occur in many chondrites. Bencubbin host metallic FeNi clasts have a positive Ni-Co trend, which coincides with that of a calculated equilibrium nebular condensation path. This appears to indicate a chondritic, rather than impact, origin for this component as well. The rare ordinary chondrite clast and dark xenolith also contain FeNi metal with compositions similar to that of the host metal. Two scenarios are offered for the origin of the Bencubbin breccia. One is that the Bencubbin components are chondritic and were produced in the solar nebula. Later brecciation, reaggregation and minor melting of the chondritic material resulted in it becoming a monomict chondritic breccia. The alternative scenario is that the Bencubbin components formed as a result of major impact melting on a chondritic parent body; the silicate fragments were formed from an impact-induced lava flow and are analogous to the spinifex-textured rocks characteristic of terrestrial komatiites. Both scenarios have difficulties, but the petrologic, chemical and isotopic data are more consistent with Bencubbin being a brecciated chondrite. Bencubbin has a number of important chemical and isotopic characteristics in common with the major components in the CR (Renazzo-type) chondrites and the unique ALH85085 chondrite, which suggests that their major components may be related. These include: (1) Mafic silicates that are similarly Mg-rich and formed in similar reducing environments. (2) Similarly low volatiles; TiO₂, Al₂O₃ and Cr₂O₃ contents are also similar. (3) Similar metallic FeNi compositions that sharply differ from those in other chondrites. (4) Remarkable enrichments in ¹⁵N. (5) Similar oxygen isotopic compositions that lie on the same mixing line. Thus, the major components of the Bencubbin breccia are highly similar to those of the ALH85085 and CR chondrites and they may have all formed in the same isotopic reservoir, under similar conditions, in the CR region of the solar nebula.     

Extraterrestrial amino acids identified in metal‐rich CH and CB carbonaceous chondrites from Antarctica

Carbonaceous chondrites contain numerous indigenous organic compounds and could have been an important source of prebiotic compounds required for the origin of life on Earth or elsewhere. Extraterrestrial amino acids have been reported in five of the eight groups of carbonaceous chondrites and are most abundant in CI, CM, and CR chondrites but are also present in the more thermally altered CV and CO chondrites. We report the abundance, distribution, and enantiomeric and isotopic compositions of simple primary amino acids in six metal‐rich CH and CB carbonaceous chondrites that have not previously been investigated for amino acids: Allan Hills (ALH) 85085 (CH3), Pecora Escarpment (PCA) 91467 (CH3), Patuxent Range (PAT) 91546 (CH3), MacAlpine Hills (MAC) 02675 (CBb), Miller Range (MIL) 05082 (CB), and Miller Range (MIL) 07411 (CB). Amino acid abundances and carbon isotopic values were obtained by using both liquid chromatography time‐of‐flight mass spectrometry and fluorescence, and gas chromatography isotope ratio mass spectrometry. The δ¹³C/¹²C ratios of multiple amino acids fall outside of the terrestrial range and support their extraterrestrial origin. Extracts of CH chondrites were found to be particularly rich in amino acids (13–16 parts per million, ppm) while CB chondrite extracts had much lower abundances (0.2–2 ppm). The amino acid distributions of the CH and CB chondrites were distinct from the distributions observed in type 2 and 3 CM and CR chondrites and contained elevated levels of β‐, γ‐, and δ‐amino acids compared to the corresponding α‐amino acids, providing evidence that multiple amino acid formation mechanisms were important in CH and CB chondrites.     

Light noble gases in 12 meteorites from the Omani desert,Australia, Mauritania,Canada, and Sweden

We measured the concentrations and isotopic compositions of He, Ne, and Ar in 14 fragments from 12 different meteorites: three carbonaceous chondrites, six L chondrites (three most likely paired), one H chondrite, one R chondrite, and one ungrouped chondrite. The data obtained for the CV3 chondrites Ramlat as Sahmah (RaS) 221 and RaS 251 support the hypothesis of exposure age peaks for CV chondrites at approximately 9 Ma and 27 Ma. The exposure age for Shi?r 033 (CR chondrite) of 7.3 Ma is also indicative of a possible CR chondrite exposure age peak. The three L chondrites Jiddat al Harasis (JaH) 091, JaH 230, and JaH 296, which are most likely paired, fall together with Hallingeberg into the L chondrite exposure age peak of approximately 15 Ma. The two L chondrites Shelburne and Lake Torrens fall into the peaks at approximately 40 Ma and 5 Ma, respectively. The ages for Bassikounou (H chondrite) and RaS 201 (R chondrite) are approximately 3.5 Ma and 5.8 Ma, respectively. Six of the studied meteorites show clear evidence for ³He diffusive losses, the deficits range from approximately 17% for one Lake Torrens aliquot to approximately 45% for RaS 211. The three carbonaceous chondrites RaS 221, RaS 251, and Shi?r 033 all have excess ⁴He, either of planetary or solar origin. However, very high ⁴He/²⁰Ne ratios occur at relatively low ²⁰Ne/²²Ne ratios, which is unexpected and needs further study. The measured ⁴⁰Ar ages fit well into established systematics. They are between 2.5 and 4.5 Ga for the carbonaceous chondrites, older than 3.6 Ga for the L and H chondrites, and about 2.4 Ga for the R chondrite as well as for the ungrouped chondrite. Interestingly, none of our studied L chondrites has been degassed in the 470 Ma break‐up event. Using the amount of trapped ³⁶Ar as a proxy for noble gas contamination due to terrestrial weathering we are able to demonstrate that the samples studied here are not or only very slightly affected by terrestrial weathering (at least in terms of their noble gas budget).