Shock melts in QUE 94411, Hammadah al Hamra 237, and Bencubbin: Remains of the missing matrix?

Abstract— We have studied the CB carbonaceous chondrites Queen Alexandra Range (QUE) 94411, Hammadah al Hamra (HH) 237, and Bencubbin with an emphasis on the petrographical and mineralogical effects of the shock processing that these meteorite assemblages have undergone. Iron‐nickel metal and chondrule silicates are the main components in these meteorites. These high‐temperature components are held together by shock melts consisting of droplets of dendritically intergrown Fe,Ni‐metal/sulfide embedded in silicate glass, which is substantially more FeO‐rich (30–40 wt%) than the chondrule silicates (FeO <5 wt%). Fine‐grained matrix material, which is a major component in most other chondrite classes, is extremely scarce in QUE 94411 and HH 237, and has not been observed in Bencubbin. This material occurs as rare, hydrated matrix lumps with major and minor element abundances roughly similar to the ferrous silicate shock melts (and CI). We infer that hydrated, fine‐grained material, compositionally similar to these matrix lumps, was originally present between the Fe,Ni‐metal grains and chondrules, but was preferentially shock melted. Other shock‐related features in QUE 94411, HH 237, and Bencubbin include an alignment and occasionally strong plastic deformation of metal and chondrule fragments. The existence of chemically zoned and metastable Fe,Ni‐metal condensates in direct contact with shock melts indicates that the shock did not substantially increase the average temperature of the rock. Because porphyritic olivine‐pyroxene chondrules are absent in QUE 94411, HH 237, and Bencubbin, it is difficult to determine the precise shock stage of these meteorites, but the shock was probably relatively light (S2–S3), consistent with a bulk temperature increase of the assemblages of less than ?300 °C. The apparently similar shock processing of Bencubbin, Weatherford, Gujba (CB_a) and QUE 94411/HH 237 (CB_b) supports the idea of a common asteroidal parent body for these meteorites.     

The Isheyevo meteorite: Mineralogy,petrology, bulk chemistry,oxygen, nitrogen,carbon isotopic compositions,and 40Ar‐39Ar ages

Abstract— Isheyevo is a metal‐rich carbonaceous chondrite that contains several lithologies with different abundances of Fe,Ni metal (7–90 vol%). The metal‐rich lithologies with 50–60 vol% of Fe,Ni metal are dominant. The metal‐rich and metal‐poor lithologies are most similar to the CB_b and CH carbonaceous chondrites, respectively, providing a potential link between these chondrite groups. All lithologies experienced shock metamorphism of shock stage S4. All consist of similar components—Fe,Ni metal, chondrules, refractory inclusions (Ca, Al‐rich inclusions [CAIs] and amoeboid olivine aggregates [AOAs]), and heavily hydrated lithic clasts—but show differences in their modal abundances, chondrule sizes, and proportions of porphyritic versus non‐porphyritic chondrules. Bulk chemical and oxygen isotopic compositions are in the range of CH and CB chondrites. Bulk nitrogen isotopic composition is highly enriched in ¹⁵N (δ¹⁵N = 1122‰). The magnetic fraction is very similar to the bulk sample in terms of both nitrogen release pattern and isotopic profile; the non‐magnetic fraction contains significantly less heavy N. Carbon released at high temperatures shows a relatively heavy isotope signature. Similarly to CB_b chondrites, ～20% of Fe,Ni‐metal grains in Isheyevo are chemically zoned. Similarly to CH chondrites, some metal grains are Ni‐rich (>20 wt% Ni). In contrast to CB_b and CH chondrites, most metal grains are thermally decomposed into Ni‐rich and Ni‐poor phases. Similar to CH chondrites, chondrules have porphyritic and non‐porphyritic textures and ferromagnesian (type I and II), silica‐rich, and aluminum‐rich bulk compositions. Some of the layered ferromagnesian chondrules are surrounded by ferrous olivine or phyllosilicate rims. Phyllosilicates in chondrule rims are compositionally distinct from those in the hydrated lithic clasts. Similarly to CH chondrites, CAIs are dominated by the hibonite‐, grossite‐, and melilite‐rich types; AOAs are very rare. We infer that Isheyevo is a complex mixture of materials formed by different processes and under different physico‐chemical conditions. Chondrules and refractory inclusions of two populations, metal grains, and heavily hydrated clasts accreted together into the Isheyevo parent asteroid in a region of the protoplanetary disk depleted in fine‐grained dust. Such a scenario is consistent with the presence of solar wind—implanted noble gases in Isheyevo and with its comparatively old K‐Ar age. We cannot exclude that the K‐Ar system was affected by a later collisional event. The cosmic‐ray exposure (CRE) age of Isheyevo determined by cosmogenic ³⁸Ar is ～34 Ma, similar to that of the Bencubbin (CB_a) meteorite.     

Compositions of unzoned and zoned metal in the CBb chondrites Hammadah al Hamra 237 and Queen Alexandra Range 94627

Abstract— The CB_b chondrites are rare, primitive, metal‐rich meteorites that contain several features, including zoned metal, that have previously been interpreted as evidence for origins in the solar nebula. We have measured concentrations of Ni, Cu, Ga, Ru, Pd, Ir, and Au within both zoned and unzoned metal grains in the CB_b chondrites Hammadah al Hamra (HaH) 237 and Queen Alexandra Range (QUE) 94627 using laser ablation inductively coupled plasma mass spectrometry. The refractory elements Ni, Ru, and Ir are enriched in the grain cores, relative to the rims, in the zoned metal. All refractory elements are uniform across the unzoned metal grains, at concentrations that are highly variable between grains. The volatile elements Cu, Ga, and Au are usually depleted relative to chondritic abundances and are most often uniform within the grains but are sometimes slightly elevated at the outermost rim. The Pd abundances are nearly uniform, at close to chondritic abundances, in all of the metal grains. A condensation origin is inferred for both types of metal. The data support a model in which the zoned metal formed at high temperatures, in a relatively rapidly cooling nebular gas, and the unzoned metal formed at lower temperatures and at a lower cooling rate. The CB_b metal appears to have formed by a process very similar to that of the CH chondrites, but the CB_b meteorite components experienced even less thermal alteration following their formation and are among the most primitive materials known to have formed in the solar nebula.     

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.     

Rapid effects of terrestrial alteration on highly siderophile elements in the Sutter's Mill meteorite

The ¹⁸⁷Re-¹⁸⁷Os isotopic systematics of many bulk chondrites plot well beyond analytical uncertainties of a primordial isochron. Limited variations in ¹⁸⁷Os/¹⁸⁸Os, coupled with large variations in Re/Os ratios among chondrites, suggest that this apparently open-system behavior is a result of the comparatively recent gain or loss of Re and/or Os. In order to assess whether or not rapid alteration in the terrestrial environment could be responsible for open-system behavior in chondrites, four pieces of the Sutter's Mill meteorite were examined for Os isotopic systematics and abundances of highly siderophile elements. Pieces SM1 and SM2 were collected prior to a rain event, within 2 days of the fall. Pieces SM51 and SM53 were collected after a rain event. There are significant but minor relative and absolute variations in the abundances of the highly siderophile elements, as well as ¹⁸⁷Os/¹⁸⁸Os among the four pieces. Rhenium-Os isotopic data for SM1 and SM2 plot within analytical uncertainties of a primordial isochron, while powders made from SM51 and SM53 do not. These results suggest that interactions with rain caused some redistribution of Re, and to a lesser extent Os, within small pieces of the meteorite. Thus, Re-Os isotopic systematics of <dm-size pieces of chondrites must be considered susceptible to modification after only a short time on the surface, where exposed to rain.     

Highly siderophile element and osmium isotope evidence for postcore formation magmatic and impact processes on the aubrite parent body

Abstract– Aubrites exhibit a wide range of highly siderophile element (HSE—Re, Os, Ir, Ru, Rh, Pt, Pd, Au) concentrations and ¹⁸⁷Os/¹⁸⁸Os compositions. Their HSE concentrations are one to three orders of magnitude less than chondrites, with the exception of the Shallowater and Mt. Egerton samples. While most aubrites show chondritic HSE abundance ratios, significant enrichments of Pd and Re relative to Os, Ir, and Ru are observed in 12 of 16 samples. Present‐day ¹⁸⁷Os/¹⁸⁸Os ratios range from subchondritic values of 0.1174 to superchondritic values of up to 0.2263. Half of the samples have ¹⁸⁷Os/¹⁸⁸Os ratios of 0.127 to 0.130, which is in the range of enstatite chondrites. Along with the brecciated nature of aubrites, the HSE and Re‐Os isotope systematics support a history of extensive postaccretion processing, including core formation, late addition of chondritic material and/or core material and potential breakup and reassembly. Highly siderophile element signatures for some aubrites are consistent with a mixing of HSE‐rich chondritic fragments with a HSE‐free aubrite matrix. The enrichments in incompatible HSE such as Pd and Re observed in some aubrites, reminiscent of terrestrial basalts, suggest an extensive magmatic and impact history, which is supported by both the ¹⁸⁷Re‐¹⁸⁷Os isotope system and silicate‐hosted isotope systems (Rb‐Sr, K‐Ar) yielding young formation ages of 1.3–3.9 Ga for a subset of samples. Compared with other differentiated achondrites derived from small planetary bodies, aubrites show a wide range in HSE concentrations and ¹⁸⁷Os/¹⁸⁸Os, most similar to angrites. While similarities exist between the diverse groups of achondrites formed early in solar system history, the aubrite parent body(ies) clearly underwent a distinct evolution, different from angrites, brachinites, ureilites, howardites, eucrites, and diogenites.     

The Fountain Hills unique CB chondrite: Insights into thermal processes on the CB parent body

Abstract— We report the results of an extensive study of the Fountain Hills chondritic meteorite. This meteorite is closely related to the CB_a class. Mineral compositions and O‐isotopic ratios are indistinguishable from other members of this group. However, many features of Fountain Hills are distinct from the other CB chondrites. Fountain Hills contains 23 volume percent metal, significantly lower than other members of this class. In addition, Fountain Hills contains porphyritic chondrules, which are extremely rare in other CB_a chondrites. Fountain Hills does not appear to have experienced the extensive shock seen in other CB chondrites. The chondrule textures and lack of fine‐grained matrix suggests that Fountain Hills formed in a dust‐poor region of the early solar system by melting of solid precursors. Refractory siderophiles and lithophile elements are present in near‐CI abundances (within a factor of two, related to the enhancement of metal). Moderately volatile and highly volatile elements are significantly depleted in Fountain Hills. The abundances of refractory siderophile trace elements in metal grains are consistent with condensation from a gas that is reduced relative to solar composition and at relatively high pressures (10^?3bars). Fountain Hills experienced significant thermal metamorphism on its parent asteroid. Combining results from the chemical gradients in an isolated spinel grain with olivine‐spinel geothermometry suggests a peak temperature of metamorphism between 535 °C and 878 °C, similar to type‐4 ordinary chondrites.     

Rhenium and osmium systematics on iron and stony iron meteorites

Abstract— Re and Os abundances and ¹⁸⁷Os/¹⁸⁶Os isotopic ratios in 12 iron meteorites of various groups and five stony iron meteorites have been determined by an inductively coupled plasma mass spectrometry (ICP-MS). The series of iron meteorites studied have Re and Os concentrations ranging from 0.004 to 3.3 ppm and 0.03 to 41 ppm, respectively. The ¹⁸⁷Re/¹⁸⁶Os ratios in these meteorites fall between 3.0 and 6.1 and the ¹⁸⁷Os/¹⁸⁶Os between 1.0 and 1.2, giving an initial ¹⁸⁷Os/¹⁸⁶Os isotopic ratio of 0.790 and a Re-Os age of iron meteorites of 4.30 ± 0.28 Ga when employing the decay constant of 1.64 × 10^?11 yr^?1. The observed Re-Os age for iron meteorites appears somewhat younger than that for chondrites. The resultant younger age might be due either to a very slow cooling of the parental planetesimals or due to a secondary “shock” event. However, for definite conclusions about the Re-Os age, higher precisions of the Re and Os isotopic measurements and of the decay constant of ¹⁸⁷Re are required. Furthermore, the clear elucidation of the mechanisms for the fractionation of the Re/Os abundance ratios are related to the understanding of the meaning of the Re-Os age. The Re and Os abundances in pallasite stony iron meteorites are extremely low compared with those for most iron meteorites. On the other hand, the Re and Os abundances in mesosiderite stony iron meteorites show values comparable with those observed in most iron meteorites. The difference in Re and Os abundances in pallasite and mesosiderite stony iron meteorites strongly suggests that these stony iron meteorites are different in origin or history of chemical evolution. Re and Os abundances in the series of iron and stony iron meteorites were found to have a wide variation covering nearly four orders of magnitude, with a very high correlation coefficient (0.996), and a slope very slightly less than unity. The regression line observed here covers various groups of iron meteorites, stony iron meteorites and also chondrites. Masuda and Hirata (1991) suggested the possible direct mixing process of particles of most refractory metallic elements with gaseous clouds of less refractory matrix elements, since the Re and Os were predicted theoretically to be the first elements to condense as a solid phase from the high temperature solar nebula. The aims of this paper are to present a reliable technique for the Re-Os chronology and to study the cosmochemical sequences of the meteoritic metals.     

Highly siderophile and chalcogen element constraints on the origin of components of the Allende and Murchison meteorites

¹⁸⁷Re‐¹⁸⁷Os systematics, abundances of highly siderophile elements (HSE: Re, PGE, and Au), chalcogen elements (Te, Se, and S), and some major and minor elements were determined in physically separated components of the Allende (CV3) and Murchison (CM2) carbonaceous chondrites. Substantial differences exist in the absolute and relative abundances of elements in the components, but the similarity of calculated and literature bulk rock abundances of HSE and chalcogens indicate that chemical complementarity exists among the components, with CI chondrite‐like ratios for many elements. Despite subsequent alteration and oxidation, the overall cosmochemical behavior of most moderately to highly siderophile elements during high‐temperature processing has been preserved in components of Allende at the sampling scale of the present study. The ¹⁸⁷Re‐¹⁸⁷Os systematics and element variations of Allende are less disturbed compared with Murchison, which reflects different degrees of oxidation and alteration of these meteorites. The HSE systematics (with the exception of Au) is controlled by two types of materials: Pd‐depleted condensates and CI chondrite‐like material. Enrichment and heterogeneous distribution of Au among the components is likely the result of hydrothermal alteration. Chalcogen elements are depleted compared with HSE in all components, presumably due to their higher volatility. Small systematic variations of S, Se, and Te in components bear the signature of fractional condensation/partial evaporation and metal–sulfide–silicate partitioning.     

Highly siderophile element and 187Re‐187Os isotopic systematics of ungrouped achondrite Northwest Africa 7325: Evidence for complex planetary processes

The abundances of highly siderophile elements (HSE; including Re, Os, Ir, Ru, Pt, and Pd) and ¹⁸⁷Re‐¹⁸⁷Os isotopic systematics were determined for two fragments from ungrouped achondrite NWA 7325. Rhenium‐Os systematics are consistent with closed‐system behavior since formation or soon after. The abundances of the HSE were therefore largely unaffected by late‐stage secondary processes such as shock or terrestrial weathering. As an olivine gabbro cumulate, this meteorite has a bulk composition consistent with derivation from a body that produced a core, mantle, and crust. Also consistent with derivation from a body that produced a core, both fragments of NWA 7325 have HSE abundances that are highly depleted compared to bulk chondrites. One fragment has ~0.002× CI chondrite Ir and relative HSE abundances similar to bulk chondrites. The other fragment has ~0.0002× CI chondrite Ir and relative HSE abundances that are fractionated compared to bulk chondrites. The chondritic relative HSE abundances of the fragment characterized by higher HSE abundances most likely reflect the addition of exogenous chondritic material during or after crystallization by surface impacts. The HSE in the other fragment is likely more representative of the parent body crust. One formation model that can broadly account for the HSE abundances in this fragment is multiple episodes of low‐pressure metal‐silicate equilibration, followed by limited late accretion and mantle homogenization. Given the different HSE compositions of the two adjoining fragments, this meteorite provides an example of the overprint of global processes (differentiation and late accretion) by localized impact contamination.     

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.     

The CR chondrite clan: Implications for early solar system processes

Abstract— In this paper, we review the mineralogy and chemistry of calcium‐aluminum‐rich inclusions (CAIs), chondrules, FeNi‐metal, and fine‐grained materials of the CR chondrite clan, including CR, CH, and the metal‐rich CB chondrites Queen Alexandra Range 94411, Hammadah al Hamra 237, Bencubbin, Gujba, and Weatherford. The members of the CR chondrite clan are among the most pristine early solar system materials, which largely escaped thermal processing in an asteroidal setting (Bencubbin, Weatherford, and Gujba may be exceptions) and provide important constraints on the solar nebula models. These constraints include (1) multiplicity of CAI formation; (2) formation of CAIs and chondrules in spatially separated nebular regions; (3) formation of CAIs in gaseous reservoir(s) having ¹⁶O‐rich isotopic compositions; chondrules appear to have formed in the presence of ¹⁶O‐poor nebular gas; (4) isolation of CAIs and chondrules from nebular gas at various ambient temperatures; (5) heterogeneous distribution of ²⁶Al in the solar nebula; and (6) absence of matrix material in the regions of CAI and chondrule formation.     

Minor and trace element concentrations in adjacent kamacite and taenite in the Krymka chondrite

We report in situ NanoSIMS siderophile minor and trace element abundances in individual Fe‐Ni metal grains in the unequilibrated chondrite Krymka (LL3.2). Associated kamacite and taenite of 10 metal grains in four chondrules and one matrix metal were analyzed for elemental concentrations of Fe, Ni, Co, Cu, Rh, Ir, and Pt. The results show large elemental variations among the metal grains. However, complementary and correlative variations exist between adjacent kamacite‐taenite. This is consistent with the unequilibrated character of the chondrite and corroborates an attainment of chemical equilibrium between the metal phases. The calculated equilibrium temperature is 446 ± 9 °C. This is concordant with the range given by Kimura et al. (2008) for the Krymka postaccretion thermal metamorphism. Based on Ni diffusivity in taenite, a slow cooling rate is estimated of the Krymka parent body that does not exceed ~1K Myr^?1, which is consistent with cooling rates inferred by other workers for unequilibrated ordinary chondrites. Elemental ionic radii might have played a role in controlling elemental partitioning between kamacite and taenite. The bulk compositions of the Krymka metal grains have nonsolar (mostly subsolar) element/Ni ratios suggesting the Fe‐Ni grains could have formed from distinct precursors of nonsolar compositions or had their compositions modified subsequent to chondrule formation events.     

Petrology and Raman spectroscopy of high pressure phases in the Gujba CB chondrite and the shock history of the CB parent body

Abstract– High pressure phases majorite, possibly majorite‐pyrope_ss, wadsleyite, and coesite are present in the matrix and in barred olivine fragments in the Gujba CB chondrite. Grossular‐pyrope was also observed in some small inclusions. The CB chondrites are metal‐rich meteorites with characteristics that sharply distinguish them from other chondrite groups. All of the CB chondrites contain impact melt regions interstitial to their chondrules, fragments and metal and a major impact event (or events), on the CB chondrite parent body is clearly a significant stage in its history. We studied three areas interstitial to chondrules and metal in the Gujba CB_a chondrite. From Raman spectra, the barred olivine fragments and matrix in these regions have various combinations of olivine and low‐Ca pyroxene, as well as majorite garnet (Mg₄Si₄O₁₂), a phase that forms by high‐pressure transformation of low‐Ca pyroxene and wadsleyite, a high pressure product of olivine. Compositions of the majorite suggest both majorite and majorite‐pyrope solid solution may be present. The mineral assemblage of majorite and wadsleyite suggest minimum shock pressures and temperatures of ～19 GPa and ～2000 °C, respectively. The occurrences of high pressure phases are variable from one area to another, on the scale of millimeters or less, suggesting heterogeneous distribution of shock and/or back transformation to low pressure polymorphs throughout the meteorite. The high pressure phases record a high temperature–pressure impact event that is superimposed onto, and thus postdates formation of, the chondrules and other components in the CB chondrites. The barred chondrules and metal in the CB chondrites are primary materials formed prior to the impact event either generated in an earlier planetesimal scale impact event or in the nebula.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

Pb‐Pb dating of individual chondrules from the CBa chondrite Gujba: Assessment of the impact plume formation model

The CB chondrites are metal‐rich meteorites with characteristics that sharply distinguish them from other chondrite groups. Their unusual chemical and petrologic features and a young formation age of bulk chondrules dated from the CB_a chondrite Gujba are interpreted to reflect a single‐stage impact origin. Here, we report high‐precision internal isochrons for four individual chondrules of the Gujba chondrite to probe the formation history of CB chondrites and evaluate the concordancy of relevant short‐lived radionuclide chronometers. All four chondrules define a brief formation interval with a weighted mean age of 4562.49 ± 0.21 Myr, consistent with its origin from the vapor‐melt impact plume generated by colliding planetesimals. Formation in a debris disk mostly devoid of nebular gas and dust sets an upper limit for the solar protoplanetary disk lifetime at 4.8 ± 0.3 Myr. Finally, given the well‐behaved Pb‐Pb systematics of all four chondrules, a precise formation age and the concordancy of the Mn‐Cr, Hf‐W, and I‐Xe short‐lived radionuclide relative chronometers, we propose that Gujba may serve as a suitable time anchor for these systems.     

Radiogenic isotope investigation of the St‐Robert H5 fall

Abstract— The St‐Robert H5 chondrite yields a mineral/whole‐rock Pb‐Pb age of 4565 ± 23 Ma (2σ) comparable to the accepted age of most chondrites. The regression of chondrule data give a similar age of 4566 ± 7 Ma (2σ). These results imply that no major perturbation affected the Pb‐Pb systematics of this meteorite's parent body within the first few billion years following its accretion. Re and Os concentrations along with Os isotopic compositions of whole‐rock fragments, surface fusion crusts and metal phases are also reported. The whole rock measurements for this ordinary chondrite are characterized by high Re/Os ratio coupled with relatively high ¹⁸⁷Os/¹⁸⁸Os (compared to average ordinary chondrites), that we interpret as a long term Re enrichment. As for most chondrites, no precise geochronological information could be extracted from the Re/Os systematics, although most data plot near the IIIAB reference isochron (Smoliar et al. 1996). From the fusion crust results, we rule out the possibility that atmospheric entry caused the perturbations in the Re‐Os system, since melted crust analysis yields among the most concordant data points. Evidence from metal phases suggests that a very recent process perturbed the isochron, relocating Re from kamacite toward troilite.     

Target rocks,impact glasses,and melt rocks from the Lonar crater,India: Highly siderophile element systematics and Sr‐Nd‐Os isotopic signatures

The Lonar crater is a ~0.57‐Myr‐old impact structure located in the Deccan Traps of the Indian peninsula. It probably represents the best‐preserved impact structure hosted in continental flood basalts, providing unique opportunities to study processes of impact cratering in basaltic targets. Here we present highly siderophile element (HSE) abundances and Sr‐Nd and Os isotope data for target basalts and impactites (impact glasses and impact melt rocks) from the Lonar area. These tools may enable us to better constrain the interplay of a variety of impact‐related processes such as mixing, volatilization, and contamination. Strontium and Nd isotopic compositions of impactites confirm and extend earlier suggestions about the incorporation of ancient basement rocks in Lonar impactites. In the Re‐Os isochron plot, target basalts exhibit considerable scatter around a 65.6 Myr Re‐Os reference isochron, most likely reflecting weathering and/or magma replenishment processes. Most impactites plot at distinctly lower ¹⁸⁷Re/¹⁸⁸Os and ¹⁸⁷Os/¹⁸⁸Os ratios compared to the target rocks and exhibit up to two orders of magnitude higher abundances of Ir, Os, and Ru. Moreover, the impactites show near‐chondritic interelement ratios of HSE. We interpret our results in terms of an addition of up to 0.03% of a chondritc component to most impact glasses and impact melt rocks. The magnitude of the admixture is significantly lower than the earlier reported 12–20 wt% of extraterrestrial component for Lonar impact spherules, reflecting the typical difference in the distribution of projectile component between impact glass spherules and bulk impactites.     

Confirmation of a meteoritic component in impact‐melt rocks of the Chesapeake Bay impact structure,Virginia, USA—Evidence from osmium isotopic and PGE systematics

Abstract— The osmium isotope ratios and platinum‐group element (PGE) concentrations of impact‐melt rocks in the Chesapeake Bay impact structure were determined. The impact‐melt rocks come from the cored part of a lower‐crater section of suevitic crystalline‐clast breccia in an 823 m scientific test hole over the central uplift at Cape Charles, Virginia. The ¹⁸⁷Os/¹⁸⁸Os ratios of impact‐melt rocks range from 0.151 to 0.518. The rhenium and platinum‐group element (PGE) concentrations of these rocks are 30–270x higher than concentrations in basement gneiss, and together with the osmium isotopes indicate a substantial meteoritic component in some impact‐melt rocks. Because the PGE abundances in the impact‐melt rocks are dominated by the target materials, interelemental ratios of the impact‐melt rocks are highly variable and nonchondritic. The chemical nature of the projectile for the Chesapeake Bay impact structure cannot be constrained at this time. Model mixing calculations between chondritic and crustal components suggest that most impact‐melt rocks include a bulk meteoritic component of 0.01–0.1% by mass. Several impact‐melt rocks with lowest initial ¹⁸⁷Os/¹⁸⁸Os ratios and the highest osmium concentrations could have been produced by additions of 0.1%–0.2% of a meteoritic component. In these samples, as much as 70% of the total Os may be of meteoritic origin. At the calculated proportions of a meteoritic component (0.01–0.1% by mass), no mixtures of the investigated target rocks and sediments can reproduce the observed PGE abundances of the impact‐melt rocks, suggesting that other PGE enrichment processes operated along with the meteoritic contamination. Possible explanations are 1) participation of unsampled target materials with high PGE abundances in the impact‐melt rocks, and 2) variable fractionations of PGE during syn‐ to post‐impact events.     

The condensation origin of zoned metal grains in Queen Alexandra Range 94411: Implications for the formation of the Bencubbin‐like chondrites

Abstract— Thermodynamic analysis of the compositional profiles across large chemically‐zoned Fe, Ni metal grains in the Bencubbin‐like chondrite Queen Alexandra Range (QUE) 94411 suggests that these grains formed by non‐equilibrium gas‐solid condensation under variable oxidizing conditions, isolation degree, and Cr depletion factors. The oxidizing conditions must have resulted from the complete vaporization of nebular regions with enhanced dust/gas ratios (～ 10–40 × solar). Because the origin of each of the metal grains studied requires different condensation parameters (dust/gas ratio, isolation degree, and Cr depletion factor), a high degree of heterogeneity in the formation region of the Bencubbin‐like chondrite metal is required. To preserve compositional zoning of the metal grains and prevent their melting and sulfidization, the grains must have been removed from the hot condensation region into cold regions where the accretion of the Bencubbin‐like asteroidal body took place.