Carbonaceous xenoliths in the Krymka LL3.1 chondrite: Mysteries and established facts

The results of a detailed study on mineralogy, chemistry, and the carbon and oxygen isotopes of two exotic Krymka carbonaceous xenoliths are presented in this article. The investigated xenoliths are metamorphosed and shocked and have the following characteristics, which distinguish them from the Krymka host: 1. resemblance of their SiO₂/MgO ratio to that of carbonaceous chondrites; 2. higher Fe content and FeO/(FeO + MgO) ratio; 3. lower concentration of Si, Ca, Al and an enrichment of S and probably of Ag; 4. smaller sizes and lower content (10 vol%) of chondrules and their clasts, and correspondingly higher content of matrix; 5. dominance of porphyritic chondrules and lack of nonporphyritic chondrules; 6. occurrence of an amoeboid olivine grain with ¹⁶O-rich composition; 7. existence of carbon in three different forms: graphite, carbon-rich material, and organic compounds.The bulk chemistry of the xenoliths is similar, but not identical, to that of carbonaceous chondrites, suggesting that they represent a chondrite parent body that has not been previously sampled. Among any known type of meteoritic material the mineralogy of the xenoliths corresponds only to that of other Krymka graphite-containing xenoliths. It differs, however, from the latter by having a lower grade of metamorphism. We infer that metamorphism of the primary carbonaceous body of the xenoliths and/or shock of the Krymka parent body are responsible for the major metamorphic alteration of the xenoliths, including the crystallization of graphite from primary organic compounds.A comparison of the features of the Krymka xenoliths with the inferred characteristics of cometary meteorites attests that their genetic relationship to cometary material remains highly inconclusive.     

Electron microprobe study of a ‘mysterite’-bearing inclusion from the Krymka LL-chondrite

The black inclusion from the Krymka LL3 chondrite previously found to contain ‘mysterite’ by Lewiset al. (1979) belongs to a hitherto unknown class of carbonaceous chondrites. Its olivine and pyroxene compositions. Fo 97–99 and En 96, respectively, are characteristic of carbonaceous chondrites and its plagioclase composition. An 100, is characteristic of C3's. It contains a peculiar group of Co-, Cr-rich metal grains whose compositions are similar, but not identical, to those in C2 chondrites and which also bear some similarities to those in Renazzo. Its weight ratios of total $\text{Fe}\text{SiO}{}_2$ and $\text{solSiO}{}_2\text{MgO}$ are 0.74 and 1.43, respectively, and its atomic ratio of $\text{Si}\text{Al}$ is 10.7, exactly the same as in carbonaceous chondrites. Its bulk chemical composition is very close to that of the Murchison C2 chondrite. The association of mysterite with a special type of carbonaceous chondrite material suggests that mysterite formed by low-temperature condensation in a different region of the nebula from other carbonaceous chondrites.     

Presolar diamond, silicon carbide, and graphite in carbonaceous chondrites: implications for thermal processing in the solar nebula

We have determined abundances of presolar diamond, silicon carbide, graphite, and Xe-P1 (Q-Xe) in eight carbonaceous chondrites by measuring the abundances of noble gas tracers in acid residues. The meteorites studied were Murchison (CM2), Murray (CM2), Renazzo (CR2), ALHA77307 (CO3.0), Colony (CO3.0), Mokoia (CV3_ox), Axtell (CV3_ox), and Acfer 214 (CH). These data and data obtained previously by Huss and Lewis (1995) provide the first reasonably comprehensive database of presolar-grain abundances in carbonaceous chondrites. Evidence is presented for a currently unrecognized Ne-E(H) carrier in CI and CM2 chondrites.After accounting for parent-body metamorphism, abundances and characteristics of presolar components still show large variations across the classes of carbonaceous chondrites. These variations correlate with the bulk compositions of the host meteorites and imply that the same thermal processing that was responsible for generating the compositional differences between the various chondrite groups also modified the initial presolar-grain assemblages. The CI chondrites and CM2 matrix have the least fractionated bulk compositions relative to the sun and the highest abundances of most types of presolar material, particularly the most fragile types, and thus are probably most representative of the material inherited from the sun's parent molecular cloud. The other classes can be understood as the products of various degrees of heating of bulk molecular cloud material in the solar nebula, removing the volatile elements and destroying the most fragile presolar components, followed by chondrule formation, metal-silicate fractionation in some cases, further nebula processing in some cases, accretion, and parent body processing. If the bulk compositions and the characteristics of the presolar-grain assemblages in various chondrite classes reflect the same processes, as seems likely, then differential condensation from a nebula of solar composition is ruled out as the mechanism for producing the chondrite classes. Presolar grains would have been destroyed if the nebula had been completely vaporized. Our analysis shows that carbonaceous chondrites reflect all stages of nebular processing and thus are no more closely related to one another than they are to ordinary and enstatite chondrites.     

Zn and Cu isotopic variations in chondrites and iron meteorites: Early solar nebula reservoirs and parent-body processes

High-precision Zn isotopic variations are reported for carbonaceous chondrites (CC), equilibrated (EOC) and unequilibrated (UOC) ordinary chondrites, iron meteorites from the IAB-IIICD (nonmagmatic) and IIIA (magmatic) groups, and metal from the Brenham pallasite. For irons, δ⁶⁵Cu values are also reported. Data have also been obtained on a coarse-grained type-B calcium-, aluminum-rich refractory inclusion (CAI) from Allende and on acid leaches of Allende (CV3), Krymka (LL3), and Charsonville (H6). Variations expressed as δ⁶⁶Zn (deviation in parts per thousand of ⁶⁶Zn/⁶⁴Zn in samples relative to a standard) spread over a range of 0.3‰ for carbonaceous chondrites, 2‰ for ordinary chondrites, and 4‰ for irons.The measured ⁶⁶Zn/⁶⁴Zn, ⁶⁷Zn/⁶⁴Zn, and ⁶⁸Zn/⁶⁴Zn ratios vary linearly with mass difference and define a common isotope fractionation line with terrestrial samples, which demonstrates that Zn was derived from an initially single homogeneous reservoir. The δ⁶⁶Zn values are correlated with meteorite compositions and slightly decrease in the order CI, CM, CV-CO, and to UOC. The isotopically light Zn of Allende CAI and the acid-resistant residues of Allende and Krymka show that the light component is associated with refractory material, presumably minerals from the spinel-group. This, together with the reverse correlation between relative abundances of light Zn isotopes and volatile element abundances, suggests that Zn depletion in planetary bodies with respect to CI cannot be ascribed to devolatilization of CI-like material. These observations rather suggest that refractory material reacted with a gas phase enriched in the lighter Zn isotopes. Alternatively, chondrules with their associated rims should carry a light Zn isotopic signature. The δ⁶⁶Zn values of unequilibrated chondrites are rather uniform, whereas equilibrated chondrites show distinctly more isotopic variability.The values of δ⁶⁵Cu-δ⁶⁶Zn in irons define two trends. The moderate and positively correlated Cu and Zn isotope variations in IIIA and pallasite samples probably reflect crystallization of silicate, sulfide, and solid metal from the liquid metal. The range of δ⁶⁶Zn values of the IAB-IIICD group is large (>3‰) and contrasts with the moderate fractionation of Cu isotopes. We interpret this feature and the negative δ⁶⁶Zn-δ⁶⁵Cu correlation as reflecting mixing, possibly achieved by percolation, between metals from a regolith devolatilized at low temperature (enriched in heavy zinc) and metallic liquids formed within the parent body.     

Carbonaceous matter in mantle xenoliths: Composition and relevance to the isotopes

Carbonaceous matter in xenoliths from alkalic basalts is present as particles in prominent cracks and as a semicontinuous film on microcracks. The particles are partially chlorinated, contain detectable amounts of Si and K, are thought to be the host phase for Rb, La and other minor and trace elements known from leaching experiments to be concentrated in microcracks and are believed to consist dominantly of graphite intercalation compounds. The carbonaceous films have been characterized by x-ray photoelectron spectroscopy. The films consist of complex mixtures of organic and possibly graphitic compounds and may include alcohols, organic acids, or other compounds unstable at elevated temperature. Nitrogen is frequently observed in photoelectron spectra of the films.Most cracks in xenoliths are likely to have developed during quenching, resulting in the exposure of chemically active surfaces. The carbonaceous films formed on them abiotically by condensation from hot volcanic gas and the low-temperature compounds formed by evolution from simpler high-temperature condensates during cooling. Such a process may have represented one step in the chemical evolution of life.The bulk of the C and other elements on crack surfaces should be regarded as contaminants from the host lava. Therefore, stepped heating procedures are necessary for the generation of meaningful isotopic data for C, N and H in xenoliths.     

Oxygen isotopic composition of chondritic interplanetary dust particles: A genetic link between carbonaceous chondrites and comets

Oxygen isotopes were measured in four chondritic hydrated interplanetary dust particles (IDPs) and five chondritic anhydrous IDPs including two GEMS-rich particles (Glass embedded with metal and sulfides) by a combination of high precision and high lateral resolution ion microprobe techniques.All IDPs have isotopic compositions tightly clustered around that of solar system planetary materials. Hydrated IDPs have mass-fractionated oxygen isotopic compositions similar to those of CI and CM carbonaceous chondrites, consistent with hydration of initially anhydrous protosolar dust. Anhydrous IDPs have small ¹⁶O excesses and depletions similar to those of carbonaceous chondrites, the largest ¹⁶O variations being hosted by the two GEMS-rich IDPs. Coarse-grained forsteritic olivine and enstatite in anhydrous IDPs are isotopically similar to their counterparts in comet Wild 2 and in chondrules suggesting a high temperature inner solar system origin. The small variations in the ¹⁶O content of GEMS-rich IDPs suggest that most GEMS either do not preserve a record of interstellar processes or the initial interstellar dust is not ¹⁶O-rich as expected by self-shielding models, although a larger dataset is required to verify these conclusions.Together with other chemical and mineralogical indicators, O isotopes show that the parent-bodies of carbonaceous chondrites, of chondritic IDPs, of most Antarctic micrometeorites, and comet Wild 2 belong to a single family of objects of carbonaceous chondrite chemical affinity as distinct from ordinary, enstatite, K- and R-chondrites. Comparison with astronomical observations thus suggests a chemical continuum of objects including main belt and outer solar system asteroids such as C-type, P-type and D-type asteroids, Trojans and Centaurs as well as short-period comets and other Kuiper Belt Objects.     

A light,chondritic xenolith in the Murchison (CM) chondrite – Formation by fluid-assisted percolation during metasomatism?

The main mineralogical characteristics of a large light-colored clast within the Murchison CM breccia are discussed in detail including data on the mineralogy, bulk chemistry, organics, and oxygen isotopes. Petrographic study shows that the white clast consists of two areas with different granoblastic textures: (1) a coarse-grained (average grain size: ∼200 μm) and (2) a fine-grained lithology (average grain-size: ∼20 μm). The Fa-content of olivine in the clast is the same as Fa within olivine from Rumuruti (R) chondrites (Fa: ∼38 mol%); however, the concentrations of the elements Ni and Ca in olivine are significantly different. The fragment also contains Ca-rich pyroxene, ∼An_30-38-plagioclase/maskelynite, Cr-rich spinel, several sulfide phases, a nepheline-normative glass, and traces of merrillite and metal. The occurrence of maskelynite and nepheline-normative amorphous phase in restricted areas of the well-recrystallized rock may indicate remarkable P-T-excursions during shock metamorphism. The O-isotope composition of the clast falls below the terrestrial fractionation line (TFL), lying in the field of CM chondrites and is significantly different from data for bulk R chondrites. The study of the soluble organic matter revealed a highly-oxidized carbon chemistry and organomagnesium compounds reflecting high temperature and pressure processes.     

The composition of carbonaceous chondrite matrix

Matrix compositions of 32 carbonaceous chondrites have been analyzed by an electron microprobe defocussed-beam technique. Except in those chondrites that show evidence of metamorphism, matrices are compositionally similar and have correlation coefficients of +0.96 or greater. Weight per cent Mg/Si in matrices is constant (0.82 ± 0.05) but less than ratios derived from bulk analyses. Matrices in metamorphosed meteorites are Mg-depleted relative to those of other chondrites. Al Rais and Renazzo (anomalous by any classification scheme) have Mg-enriched matrices. Average matrix compositions cluster into chemical subgroups similar to those based on bulk chemical and petrographie criteria [C1, C2, C3(0), C3(V)]. C1 matrices are particularly variable in composition from point to point within the same meteorite, but points within individual breccia clasts appear to be more compositionally uniform. Cl matrices are depleted in Na, S, and Ca relative to solar and C2 matrix values, probably as a result of leaching. Matrix Ca/A1 ratios are highly variable and generally fall below the accepted meteoritic value. The only strong interelement correlation is for Fe, Ni, and S in C2 matrices, suggesting mixing of variable proportions of two components: Mg-rich phyllosilicate and a Ni-bearing chalcophile phase. The amount of magnetite associated with C2 matrix appears to vary systematically with matrix composition. Isotopic, chemical, and mineralogical constraints suggest that matrix, although appreciably altered in some meteorites, is chiefly a solar system condensation product which contains an admixture of unprocessed interstellar dust.     

Rhodium, gold and other highly siderophile element abundances in chondritic meteorites

The abundances of the highly siderophile elements (HSE) Re, Os, Ir, Ru, Pt, Rh, Pd and Au, and ¹⁸⁷Os/¹⁸⁸Os isotope ratios have been determined for a set of carbonaceous, ordinary, enstatite and Rumuruti chondrites, using an analytical technique that permits the precise and accurate measurement of all HSE from the same digestion aliquot. Concentrations of Re, Os, Ir, Ru, Pt and Pd were determined by isotope dilution ICP-MS and N-TIMS analysis. The monoisotopic elements Rh and Au were quantified relative to the abundance of Ir.Differences in HSE abundances and ratios such as Re/Os, ¹⁸⁷Os/¹⁸⁸Os, Pd/Ir and Au/Ir between different chondrite classes are further substantiated with new data, and additional Rh and Au data, including new data for CI chondrites. Systematically different relative abundances of Rh between different chondrite classes are reminiscent of the behaviour of Re. Carbonaceous chondrites are characterized by low average Rh/Ir of 0.27 ± 0.03 (1s) which is about 20% lower than the ratio for ordinary (0.34 ± 0.02) and enstatite chondrites (EH: 0.33 ± 0.01; EL: 0.32 ± 0.01). R chondrites show higher and somewhat variable Rh/Ir of 0.37 ± 0.07.Well-defined linear correlations of HSE, in particular for bulk samples of ordinary and EL chondrites, are explained by binary mixing and/or dilution by silicates. The HSE carriers responsible for these correlations have a uniform chemical composition, indicating efficient homogenization of local nebular heterogeneities during or prior to the formation of the host minerals in chondrite components. Excepting Rumuruti chondrites and Au in carbonaceous chondrites, these correlations also suggest that metamorphism, alteration and igneous processes had negligible influence on the HSE distribution on the bulk sample scale.Depletion patterns for Rh, Pd and Au in carbonaceous chondrites other than CI are smoothly related to condensation temperatures and therefore consistent with the general depletion of moderately volatile elements in carbonaceous chondrites. Fractionated HSE abundance patterns of ordinary, enstatite and Rumuruti chondrites, however, are more difficult to explain. Fractional condensation combined with the removal of metal phases at various times, and later mixing of early and late formed metal phases may provide a viable explanation. Planetary fractionation processes that may have affected precursor material of chondrite components cannot explain the HSE abundance patterns of chondrite groups. HSE abundances of some, but not all Rumuruti chondrites may be consistent with solid sulphide-liquid sulphide fractionation processes during impact induced melting.     

Chemical,isotopic and amino acid composition of Mukundpura CM2.0(CM1) chondrite: Evidence of parent body aqueous alteration

The carbonaceous chondrites are intriguing and unique in the sense that they are the only rocks that provide pristine records of the early solar nebular processes. We report here results of a detailed mineralogical, chemical, amino acid and isotopic studies of a recently observed fall at Mukundpura, near Jaipur in Rajasthan, India. Abundance of olivines in this meteorite is low and of serpentine minerals is high. FeO/SiO_2 = 1.05 in its Poorly Characterized Phases(PCP) is similar to that observed in other CM2.0 chondrites. The water content of ～9.8 wt.% is similar to that found in many other CM chondrites.Microscopic examination of matrix shows that its terrestrial weathering grade is WO but aqueous parent body alteration is high, as reflected in low abundance of identifiable chondrules and abundant remnants of chondrules(～7%). Thus, most of the chondrules formed initially have been significantly altered or dissolved by aqueous alterations on their parent bodies. The measured bulk carbon(2.3%) and nitrogen content and their isotopic(δ¹³C =-5.5‰, δ¹⁵N = 23.6%0) composition is consistent with CM2.0 classification probably bordering CM1. Several amino acids such as Alanine, Serine, Proline, Valine, Threonine,Leucine, Isoleucine, Asparagine and Histamine are present. Tyrosine and Tryptophan may occur in trace amounts which could not be precisely determined. All these data show that Mukundpura chondrite lies at the boundary of CM2.0 and CM1 type carbonaceous chondrites making it one of the most primitive chondrites.     

Coupled Cu and O excesses in chondrites

Recent developments in multiple-collector magnetic-sector ICP-MS (inductively coupled plasma-mass spectrometry) have permitted the relative abundances of the two isotopes 63 and 65 of copper to be measured with unprecedented precision (40 ppm). Here, we report Cu isotopic variations among eight carbonaceous chondrites (CCs) from the CI, CM, CO, and CV groups and the presently ungrouped Tagish Lake, and 10 ordinary chondrites (OCs) from the H, L, and LL groups. The widest isotopic range of ∼0.8‰ per a.m.u. is observed for the carbonaceous chondrites. Copper in carbonaceous chondrites becomes isotopically lighter with petrologic type in the order 1 to 3 but seems extremely homogeneous for each type. The Cu isotopic composition of Tagish Lake confirms its other characteristics that are intermediate between CI and CM. In three of the groups (CI-CM-CO), as well as for Tagish Lake, ⁶³Cu excess over terrestrial mantle abundances correlates well with ¹⁶O excess. For all four groups, ⁶³Cu excess also correlates remarkably well with elemental refractory/volatile ratios (e.g., Ca/Mn). For ordinary chondrites, small differences exist between the H, L, and LL groups, with Cu becoming isotopically heavier in that order. Equilibrated and unequilibrated samples, however, exhibit the same Cu isotopic signature within each group. Although the range of Cu isotopic compositions in ordinary chondrites is smaller than in carbonaceous chondrites, ⁶³Cu excesses still correlate with ¹⁶O excesses. The observed trends of isotopic variation seem incompatible with a single-stage fractionation process by either volatilization or low-temperature metamorphism. The correlations between ⁶³Cu excesses and ¹⁶O excesses suggest the presence of at least two and perhaps three isotopically distinct Cu reservoirs in the early Solar System: (1) an Earth-like reservoir common to the CI and LL probably representing the main Cu stock of the inner Solar System, (2) a reservoir present in all carbonaceous chondrites, but most abundant in CV, with large ⁶³Cu and ¹⁶O excesses (this reservoir is probably hosted in refractory material), and (3) possibly a third reservoir present in ordinary chondrites. The OC trend may also be explained as a mixture of the first two Cu reservoirs if its oxygen was first equilibrated with nebular gas. The coexistence of ⁶³Cu and ¹⁶O excesses in the same component raises the issue of how volatile Cu was preserved in refractory material. A strong correlation between ⁶³Cu/⁶⁵Cu and Ni/Cu ratios suggests that ⁶³Cu excess may have originated as more refractory ⁶³Ni (T_1/2 = 100 yr) upon irradiation of refractory grains by electromagnetic flares and particle bursts during the T-Tauri phase of the Sun.     

Aqueous alteration in carbonaceous chondrites: Mass balance constraints on matrix mineralogy

Bulk chemical compositions of matrix material in Antarctic CM chondrites and other non-Antarctic CM and CI chondrites have been determined using microprobe defocused beam techniques. These are used, along with the results of previously published mineralogical studies, to provide mass balance constraints on the relative proportions of intergrown and intermixed phyllosilicate phases in carbonaceous chondrite matrices. Results of these calculations indicate differing amounts of PCP (a mixture of approximately 25% tochilinite and 75% cronstedtite) and serpentines (Mg-rich and Fe-rich varieties in varying proportions or intermediate compositional varieties). Additional sulfide phases are also probably necessary to account for excess Ni and S. Fe/Si ratios for matrices of individual meteorites range from 1.21 to 2.77, corresponding to PCP/(PCP + SERF) ratios of 0.16 to 0.58. Progressive aqueous alteration of matrix appears to have occurred by formation of tochilinite, then cronstedtite and Mg-rich serpentine, and finally Fe-rich serpentine and sulfides. CM matrix clearly did not behave as an isolated system during alteration. CI chondrite matrices appear to contain little if any PCP; this may be a natural consequence of the absence of chondrule-associated metal, from which PCP forms, in the unaltered precursor material. These data provide a more quantitative picture of low-temperature aqueous alteration processes in carbonaceous chondrite parent bodies than has heretofore been possible from TEM studies alone.     

Origin of isotopically light nitrogen in meteorites

Bulk meteorite samples of various chemical classes and petrologic types (mainly carbonaceous chondrites) were systematically investigated by the stepped combustion method with the simultaneous isotopic analysis of carbon, nitrogen, and noble gases. A correlation was revealed between planetary noble gases associating with the Q phase and isotopically light nitrogen (δ¹⁵N up to –150‰). The analysis of this correlation showed that the isotopically light nitrogen (ILN) is carried by Q. In most meteorites, isotopically heavy nitrogen (IHN) of organic compounds (macromolecular material) is dominant. The ILN of presolar grains (diamond and SiC) and Q can be detected after separation from dominant IHN. Such a separation of nitrogen from Q and macromolecular material occurs under natural conditions and during laboratory stepped combustion owing to Q shielding from direct contact with oxygen, which results in Q oxidation at temperatures higher than the temperatures of the release of most IHN. There are arguments that ILN released at high temperature cannot be related to nanodiamond and SiC. The separation effect allowed us to constrain the contents of noble gases in Q, assuming that this phase is carbon-dominated. The directly measured ³⁶Ar/C and ¹³²Xe/C ratios in ILN-rich temperature fractions are up to 0.1 and 1 × 10^–4 cm³/g, respectively. These are only lower constraints on the contents. The analysis of the obtained data on the three-isotope diagram δ¹⁵N–³⁶Ar/¹⁴N showed that Q noble gases were lost to a large extent from most meteorites during the metamorphism of their parent bodies. Hence, the initial contents of noble gases in Q could be more than an order of magnitude higher than those directly measured. Compared with other carbon phases, Q was predominantly transformed to diamond in ureilites affected by shock metamorphism. The analysis of their Ar–N systematics showed that, similar to carbonaceous chondrites, noble gases were lost from Q probably before its transformation to diamond.     

Effects of secondary alteration on the composition of free and IOM-derived monocarboxylic acids in carbonaceous chondrites

Monocarboxylic acids (MCAs) are important astrobiologically because they are often the most abundant soluble compounds in carbonaceous chondrites (CCs) and are potential synthetic end products for many biologically important compounds. However, there has been no systematic study on the effect of parent body alteration on molecular and isotopic variability of MCAs. Since MCAs in meteorites are dominated by low molecular weight (C1-C8), highly volatile compounds, their distributions are likely to be particularly sensitive to secondary alteration processes. In contrast, the aliphatic side chains of insoluble organic matter (IOM) in CCs, whose composition has been shown to be closely related to the MCAs, may be far more resistant to secondary alteration. In the present study, we determined the distributions and isotopic ratios of free and IOM-derived MCAs in six carbonaceous chondrites with a range of classifications: Murchison (CM2), EET 87770 (CR2), ALH 83034 (CM1), ALH 83033 (CM2), MET 00430 (CV3) and WIS 91600 (C2). We compare mineralogical and petrological characteristics to the MCAs distributions to better define the processes leading to the synthesis and alteration of meteoritic MCAs. Our results show that aqueous and especially thermal alteration in the parent bodies led to major loss of free MCAs and depletion of straight relative to branched chain compounds. However, the MCAs derived from aliphatic side chains of IOM are well preserved despite of secondary alterations. The molecular and isotopic similarities of IOM-derived MCAs in different chondrite samples indicate very similar synthetic histories for organic matter in different meteorites.     

Oxygen isotope cosmothermometer revisited

A previously published estimate of the oxygen isotopic composition of the gas of the early solar nebula must be revised in light of the discovery of non-chemical isotope effects in carbonaceous chondrites. The solids which accreted to form the Earth, Moon and ordinary chondrites probably did not equilibrate isotopically with the gas below 1000 K.     

Metal and associated phases in Krymka and Chainpur: Nebular formational processes

The highly unequilibrated LL3 chondrites Krymka and Chainpur preserve a relatively unaltered record of formation in the solar nebula in the texture and chemistry of their opaque mineral assemblages. A moderate degree of diversity among these meteorites and Bishunpur is apparently associated with formation under differing conditions.Spheroidal kamacite, some Cr-bearing, is present in chondrule interiors. Fine-grained metal within the Fe-rich opaque matrix of Krymka consists exclusively of taenite and minor tetrataenite; kamacite occurs inside metal-sulfide nodules. These nodules are surrounded by an inner layer of FeO-rich, fine-grained silicate material (FeO/(FeO + MgO) > 80%) and an outer troilite-rich layer, and contain variable amounts of a hydrated Fe-oxide phase. It appears that the nodules were melted, often incompletely, possibly during the chondrule formation process. Some nodule metal is Si- and Cr-bearing, indicating little reaction with nebular H₂O. Nodules are much less common in Chainpur than in Krymka and rare in Bishunpur.Most metal-poor chondrules in Krymka, Bishunpur and Chainpur appear to have formed from precursors that had acquired significant amounts of FeO as a result of reaction with the nebular gas down to low temperatures; metal-rich chondrules seem to have derived from aggregates of coarse, high-temperature Fe-poor silicates. Low Ni concentrations (34–41 mg/g) in chondrule kamacite may largely result from dilution by Fe reduced from the silicates during chondrule formation.The opaque silicate matrix of Krymka is considerably more oxidized than that of Bishunpur and Chainpur, it contains no kamacite and its composition is very uniform. This may either reflect the growth of silicate grains during incipient recrystallization in the matrices of Bishunpur and Chainpur or, more likely, a lower mean grain size of the Krymka matrix components, possibly indicating later formation of the Krymka parent planetesimal.     

Investigating the variations in carbon and nitrogen isotopes in carbonaceous chondrites

The carbonaceous chondrites contain significant amounts of carbon- and nitrogen-bearing components, the most abundant of which is organic matter. Stepped combustion data of whole rock and HF/HCl residues of carbonaceous chondrites reveal that the organic material can be subdivided operationally into three components: (1) free organic matter (FOM), which is readily extractable from whole-rock meteorites and is enriched in ¹³C and ¹⁵N; (2) labile organic matter (LOM), which has a macromolecular structure but is liberated by hydrous pyrolysis; LOM is the parent structure for some FOM and is also enriched in ¹³C and ¹⁵N; and (3) refractory organic matter (ROM), which is also macromolecular but is virtually unaffected by hydrous pyrolysis and is relatively depleted in ¹³C and ¹⁵N. The macromolecular entities (LOM and ROM) are by far the most abundant organic components present, and as such, the relative abundances of the ¹³C- and ¹⁵N-enriched LOM and the ¹³C- and ¹⁵N-depleted ROM will have a major influence on the overall isotopic composition of the whole-rock meteorite. Laboratory experiments designed to simulate the effects of parent body aqueous alteration indicate that this form of processing removes LOM from the macromolecular material, allowing ROM to exert a stronger influence on the overall isotopic compositions. Hence, aqueous alteration of macromolecular materials on the meteorite parent body may have a significant control on the stable isotopic compositions of whole-rock carbonaceous chondrites. The enstatite chondrites are also carbon rich but have been subjected to high levels of thermal metamorphism on their parent body. Stepped combustion data of HF/HCl residues of enstatite chondrites indicate, that if they and carbonaceous chondrites inherited a common organic progenitor, metamorphism under reducing conditions appears to incorporate and preserve some of the ¹³C enrichments in LOM during graphitisation. However, when metamorphism is at its most extreme, the ¹⁵N enrichments in LOM are lost.     

The organic analysis of the murchison meteorite

The organic compounds released from the Murchison carbonaceous chondrite following vaporization-pyrolysis at 150, 300 and 430°C were investigated. The total organic yield was 272 ppm and consisted of n-alkanes, alkenes, aromatic hydrocarbons and thioaromatics. The composition and yield at all three temperatures are compared with those obtained by an identical analysis on another carbonaceous chondrite, Allende, and two terrestrial rocks.Comparison of compounds released by 150°C volatilization of Murchison and Allende reveals remarkable similarities, suggesting commonality in the processes responsible for their formation. The origin of the organic compounds found can be explained in terms of the Fischer-Tropsch synthesis followed by partial equilibration of the primary products. However, problems concerning the relationship between types of carbonaceous chondrites remain unresolved.     

Carbonaceous and non-carbonaceous lithic fragments in the Plainview,Texas, chondrite: origin and history

The Plainview. Texas, meteorite is a polymict-brecciated H-group chondrite composed of recrystallized light-colored portions embedded in a well-compacted, dense, somewhat recrystallized, dark-colored matrix. Both portions consist of equilibrated silicates (H5 classification), but a small number of silicate grains and unequilibrated lithic fragments not compatible with equilibrated ordinary H-group material are present in the dark-colored matrix. Lithic fragments include: (i) dark-colored, more or less altered, type II carbonaceous chondrites. (ii) unequilibrated ordinary chondrites and (iii) light-colored, unequilibrated and equilibrated fragments, some of which are compositionally similar to the host. Also present are fragment-like dark areas that are highly-shocked host material and not true lithic fragments (pseudo-fragments). Conclusions: Plainview represents a complex regolith breccia formed by repeated impact episodes. Recrystallized, light-colored portions represent surface or near-surface material of a small (asteroidal-sized) parent body. Impacts broke up this material to form fine-grained, dark material which enclosed light-colored protolith. Lithic fragments (i-iii) and some unequilibrated silicate grains and chondrules (apparently derived from unequilibrated chondrites) were embedded in the dark matrix during these repeated impacts. Xenolitlils of carbonaceous and unequilibrated ordinary chondrites are either residues of projectiles that impacted the Plainview parent body, or material from coexisting regoliths impact-splashed into Plainview regolith. Chondrules and silicate grains in the dark matrix which differ from H-group material are likely related to these xenoliths and their regoliths. Light-colored lithic fragments may represent shock-melted chondritic material, sometimes compositionally-modified, or new, achondritic meteoritic types. Unequilibrated and carbonaceous lithic fragments in the dark-colored host matrix indicate that equilibration of the host occurred before incorporation of the fragments and that compaction and lithification of the Plainview regolith to form a coherent meteorite must have occurred at temperatures below 300°C and/or on a short time scale.     

Deuterium enrichments in chondritic macromolecular material—Implications for the origin and evolution of organics, water and asteroids

Here we report the elemental and isotopic compositions of the insoluble organic material (IOM) isolated from several previously unanalyzed meteorites, as well as the reanalyses of H isotopic compositions of some previously measured samples (Alexander et al., 2007). The IOM in ordinary chondrites (OCs) has very large D enrichments that increase with increasing metamorphism and decreasing H/C, the most extreme δD value measured being almost 12,000‰. We propose that such large isotopic fractionations could be produced in the OC parent bodies through the loss of isotopically very light H₂ generated when Fe was oxidized by water at low temperatures (<200 °C). We suggest that similar isotopic fractionations were not generated in the IOM of CV and CO chondrites with similar metamorphic grades and IOM H/C ratios because proportionately less water was consumed during metamorphism, and the remaining water buffered the H isotopic composition of the IOM even a H was being lost from it.Hydrogen would also have been generated during the alteration of CI, CM and CR carbonaceous chondrites. The IOM in these meteorites exhibit a considerable range in isotopic compositions, but all are enriched in D, as well as ¹⁵N, relative to terrestrial values. We explore whether these enrichments could also have been produced by the loss of H₂, but conclude that the most isotopically anomalous IOM compositions in meteorites from these groups are probably closest to their primordial values. The less isotopically anomalous IOM has probably been modified by parent body processes. The response of IOM to these processes was complex and varied, presumably reflecting differences in conditions within and between parent bodies.The D enrichments associated with H₂ generation, along with exchange between D-rich IOM and water in the parent bodies, means that it is unlikely that any chondrites retain the primordial H isotopic composition of the water ice that they accreted. The H isotopic compositions of the most water-rich chondrites, the CMs and CIs, are probably the least modified and their compositions (δD ? −25‰) suggest that their water did not form at large radial distances from the Sun where ice is predicted to be very D-rich. Yet models to explain the O isotopic composition of inner Solar System bodies require that large amounts of ice were transported from the outer to the inner Solar System.