A corundum-rich inclusion in the Murchison carbonaceous chondrite

A corundum-hibonite inclusion, BB-5, has been found in the Murchison carbonaceous chondrite. This is the first reported occurrence of corundum as a major phase in any refractory inclusion, even though this mineral is predicted by thermodynamic calculations to be the first condensate from a cooling gas of solar composition. Ion microprobe measurements of Mg isotopic compositions yield the unexpected result for such an early condensate that ²⁶Mg excesses are small: δ_N²⁶Mg = 7.0 ± 1.6%. for hibonite and 5.0 ± 4.8%. for corundum, despite very large ${}^{27}\text{Al}{}^{24}\text{Mg}$ ratios, 130 and 2.74 × 10⁴, respectively. Within the errors, δ_N²⁶Mg does not vary over this exceedingly large range of ${}^{27}\text{Al}{}^{24}\text{Mg}$ ratios. The extreme temperature required to melt this inclusion makes a liquid origin unlikely, except possibly by hypervelocity impact involving refractory bodies. If, instead, BB-5 is a direct gas-solid condensate, textural evidence implies that corundum formed first and later reacted to produce hibonite. In this model, BB-5's uniform enrichment in ²⁶Mg must be a characteristic of the reservoir from which it condensed. Because severe difficulties are encountered in making such a reservoir by prior decay of ²⁶Al, nebular heterogeneity in magnesium isotopic composition is a preferred explanation.     

Isotopic characterisation of kerogen-like material in the Murchison carbonaceous chondrite

Isotopic data for C, H and N in acid-resistant residues from carbonaceous chondrites show substantial variability during stepwise pyrolysis and/or combustion. After subtraction of contributions due apparently to inorganic C grains, of probably circumstellar origin, considerable isotopic variability remains, attributable to the kerogen-like organic fraction. That variability may be interpreted in terms of three or four distinct components, based on C, H and N isotopes. The relative proportions of those components vary significantly from sample to sample. The different isotopic components are tentatively identified in terms of specific chemical/structural moieties within the kerogen-like material. This combination of chemical, structural and isotopic information suggests a complex history for meteoritic organic matter. At least three components within the organic population as a whole still carry a signature of apparently interstellar Denrichment. Part, at least, of the interstellar carrier consisted of reactive entities, not solely polymers.     

Titanium isotopic anomalies in meteorites

High-precision analyses of Ti are reported for samples from a variety of meteorite classes. The expanded data base for Allende inclusions still shows Ti isotopic anomalies in every inclusion. All the coarse-grained inclusions give quite similar patterns, but fine-grained inclusions show more variable, and sometimes larger, anomalies. One inclusion, 3675A, was analyzed because others identified it as a possible “FUN” inclusion due to its mass-fractionated Mg. This designation is supported by the significantly more complex Ti isotopic pattern for 3675A compared to all our other Allende inclusions. Available data fail to suggest that any particular Allende mineral phase, including a chromite-carbon fraction from an acid residue, is especially rich in anomalous Ti. We also find anomalous Ti in a bulk sample of a Cl chondrite and in matrix separates from C2 chondrites. The excesses of ⁵⁰Ti are smaller than for Allende inclusions, and subtle differences in Ti isotopic patterns tentatively suggest that parent materials for C1-C2 matrix and Allende inclusions are not directly related. Analyses of chondrules from unequilibrated ordinary chondrites did not yield clear evidence for anomalous Ti, but some “larger than usual” deficits at $\text{50}\text{46}$ give encouragement for future work in this direction. Comparing the magnitude of isotopic shifts at ⁵⁰Ti and ¹⁶O for all these meteorite samples indicates that they are not correlated, but the data do not preclude a correlation between concentrations of “exotic” ⁵⁰Ti and ¹⁶O atoms.Whether or not Allende “FUN” inclusions are considered, at least 4 distinct isotopic components of Ti are required to account for the observed isotopic variations. The Ti data cannot be plausibly explained in terms of an early solar-system particle irradiation; instead, neutron-rich hydrostatic burning within a star is probably responsible for the dominant ⁵⁰Ti anomalies, while s-process mechanisms are viable sources for some of the more subtle Ti variations. We suggest that the Ti anomalies are linked to a diversity of nucleosynthetic sources and the highly refractory behavior of Ti. Therefore, some form of “chemical memory” from the ISM, rather than “late stage supernova injection”, is most likely responsible for the preservation of observed isotopic heterogeneities.     

Determination of lead isotopic composition of a grain from the allende carbonaceous chondrite by LAMMA

The attempt of this work is to use the LAMMA, a newly developed modern micro-beam analytical technique, to determine the lead isotopic composition of some grains picked out from the white aggregate in the Allende (C3V) carbonaceous chondrite. The experimental results show that the Pb/Pb model age of the Allende calculated on the basis of the²⁰⁶Pb/²⁰⁷Pb ratio is 4.56 ±0.008 b. y., just in agreement with the values reported in literature. The LAMMA provides a new and powerful tool in the analytical arsenal dealing with trace elements and isotopic compositions, due to its high sensitivity, rapid performence and good space resolution.     

Microscale oxygen isotopic exchange and magnetite formation in the Ningqiang anomalous carbonaceous chondrite

We report in situ measurements of O-isotopic compositions of magnetite, olivine and pyroxene in chondrules of the Ningqiang anomalous carbonaceous chondrite. The petrographic setting of Ningqiang magnetite is similar to those in oxidized-CV chondrites such as Allende, where magnetite is found together with Ni-rich metal and sulfide in opaque assemblages in chondrules. Both magnetite and silicate oxygen data fall close to the carbonaceous-chondrite-anhydrous-mineral line with relatively large ranges in δ¹⁸O in magnetite (−4.9 to +4.2‰) and in silicates (−15.2 to −4.5‰). Magnetite and silicates are not in O-isotopic equilibrium: the weighted average Δ¹⁷O (=δ¹⁷O − 0.52 × δ¹⁸O) values of magnetite are 1.7 to 3.6‰ higher than those of the silicates in the same chondrules. The petrological characteristics and O-isotopic disequilibrium between magnetite and silicates suggest the formation of Ningqiang magnetite by the oxidation of preexisting metal grains by an aqueous fluid during parent body alteration. The weighted average Δ¹⁷O of −3.3 ± 0.3‰ is the lowest magnetite value measured in unequilibrated chondrites and there is a positive correlation between Δ¹⁷O values of magnetite and silicates in each chondrule. These observations indicate that, during aqueous alteration in the Ningqiang parent asteroid, the water/rock ratio was relatively low and O-isotopic exchange between the fluid and chondrule silicates occurred on the scale of individual chondrules.     

Presolar spinel grains from the Murray and Murchison carbonaceous chondrites

With a new type of ion microprobe, the NanoSIMS, we determined the oxygen isotopic compositions of small (<1μm) oxide grains in chemical separates from two CM2 carbonaceous meteorites, Murray and Murchison. Among 628 grains from Murray separate CF (mean diameter 0.15 μm) we discovered 15 presolar spinel and 3 presolar corundum grains, among 753 grains from Murray separate CG (mean diameter 0.45 μm) 9 presolar spinel grains, and among 473 grains from Murchison separate KIE (mean diameter 0.5 μm) 2 presolar spinel and 4 presolar corundum grains. The abundance of presolar spinel is highest (2.4%) in the smallest size fraction. The total abundance in the whole meteorite is at least 1 ppm, which makes spinel the third-most abundant presolar grain species after nanodiamonds (if indeed a significant fraction of them are presolar) and silicon carbide. The O-isotopic distribution of the spinel grains is very similar to that of presolar corundum, the only statistically significant difference being that there is a larger fraction of corundum grains with large ¹⁷O excesses (¹⁷O/¹⁶O > 1.5 × 10⁻³), which indicates parent stars with masses between 1.8 and 4.5 M_⊙.     

Re-Os isotopic systematics and platinum group element composition of the Tagish Lake carbonaceous chondrite

The Tagish Lake meteorite is a primitive C2 chondrite that has undergone aqueous alteration shortly after formation of its parent body. Previous work indicates that if this type of material was part of a late veneer during terrestrial planetary accretion, it could provide a link between atmophile elements such as H, C, N and noble gases, and highly siderophile element replenishment in the bulk silicate portions of terrestrial planets following core formation. The systematic Re-Os isotope and highly siderophile element measurements performed here on five separate fractions indicate that while Tagish Lake has amongst the highest Ru/Ir (1.63 ± 0.08), Pd/Ir (1.19 ± 0.06) and ¹⁸⁷Os/¹⁸⁸Os (0.12564-0.12802) of all carbonaceous chondrites, these characteristics still fall short of those necessary to explain the observed siderophile element systematics of the primitive upper mantles of Earth and Mars. Hence, a direct link between atmophile and highly siderophile elements remains elusive, and other sources for replenishment are required, unless an as yet poorly constrained process fractionated Re/Os, Ru/Ir, and Pd/Ir following late accretion on both the Earth and Mars mantles.The unique elevated Ru/Ir combined with elevated ¹⁸⁷Os/¹⁸⁸Os of Tagish Lake may be attributed to Ru and Re mobility during aqueous alteration very early in its parent body history. The Os, Ir, Pt, and Pd abundances of Tagish Lake are similar to CI chondrites. The elevated Ru/Ir and the higher Re/Os and consequent ¹⁸⁷Os/¹⁸⁸Os in Tagish Lake, are balanced by a lower Ru/Ir and lower Re/Os and ¹⁸⁷Os/¹⁸⁸Os in CM-chondrites, relative to CI chondrites. A model that links Tagish Lake with CI and CM chondrites in the same parent body may explain the observed systematics. In this scenario, CM chondrite material comprises the exterior, grading downward to Tagish Lake material, which grades to CI material in the interior of the parent body. Aqueous alteration intensifies towards the interior with increasing temperature. Ruthenium and Re are mobilized from the CM layer into the Tagish Lake layer. This model may thus provide a potential direct parent body relationship between three separate groups of carbonaceous chondrites.     

Mercury abundances and isotopic compositions in the Murchison (CM) and Allende (CV) carbonaceous chondrites

The abundance and isotopic composition of Hg was determined in bulk samples of both the Murchison (CM) and Allende (CV) carbonaceous chondrites using single- and multi-collector inductively coupled plasma mass spectrometry (ICP-MS). The bulk abundances of Hg are 294 ± 15 ng/g in Murchison and 30.0 ± 1.5 ng/g in Allende. These values are within the range of previous measurements of bulk Hg abundances by neutron activation analysis (NAA). Prior studies suggested that both meteorites contain isotopically anomalous Hg, with δ^196/202Hg values for the anomalous, thermal-release components from bulk samples ranging from −260 ‰ to +440 ‰ in Murchison and from −620 ‰ to +540 ‰ in Allende Jovanovic and Reed 1976a, Jovanovic and Reed 1976b, Kumar and Goel 1992. Our multi-collector ICP-MS measurements suggest that the relative abundances of all seven stable Hg isotopes in both meteorites are identical to terrestrial values within 0.2 to 0.5 ‰.On-line thermal-release experiments were performed by coupling a programmable oven with the single-collector ICP-MS. Powdered aliquots of each meteorite were linearly heated from room temperature to 900°C over twenty-five minutes under an Ar atmosphere to measure the isotopic composition of Hg released from the meteorites as a function of temperature. In separate experiments, the release profiles of S and Se were determined simultaneously with Hg to constrain the Hg distribution within the meteorites and to evaluate the possibility of Se interferences in previous NAA studies. The Hg-release patterns differ between Allende and Murchison. The Hg-release profile for Allende contains two distinct peaks, at 225° and 343°C, whereas the profile for Murchison has only one peak, at 344°C. No isotopically anomalous Hg was detected in the thermal-release experiments at a precision level of 5 to 30 ‰, depending on the isotope ratio. In both meteorites the Hg peak at ∼340°C correlates with a peak in the S-release profile. This correlation suggests that Hg is associated with S-bearing phases and, thus, that HgS is a major Hg-bearing phase in both meteorites. The Hg peak at 225°C for Allende is similar to release patterns of physically adsorbed Hg on silicate and metal grains. Prior studies suggested that the isotopic anomalies reported from NAA resulted from interference between ²⁰³Hg and ⁷⁵Se. However, the amount of Se released from both meteorites, relative to Hg, is insufficient to produce all of the observed anomalies.     

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.     

Chemical compositions of refractory inclusions in the Murchison C2 chondrite

Samples from ten refractory inclusions in Murchison, some of which are splits of inclusions whose mineralogical and petrographic characteristics are known, have been analysed for thirty-six elements by neutron activation. Six inclusions have group II or group III patterns or variants of such patterns. Two inclusions, BB-5 and MUCH-1, have large negative Yb anomalies unaccompanied by correspondingly large negative Eu anomalies. It is possible that the latter condensed originally with group III patterns and preferentially took up Eu in later exchange processes under reducing conditions. One inclusion, SH-2, has heavy REE enrichment factors that increase with the refractoriness of the REE, indicating the presence of an extremely high-temperature, or ultrarefractory, REE condensate, but it also has a heavy REE/light REE ratio that indicates mixing of that component with a lower-temperature REE condensate. The frequency of highly fractionated REE patterns and absence of group I patterns suggest that refractory inclusions in Murchison stopped equilibrating with the nebular gas at higher temperatures than most Allende coarse-grained inclusions. The lower Ir/Os and Ru/Re ratios of some Murchison inclusions compared to those of Allende coarse-grained inclusions indicate that condensate alloys that contributed noble metals to the former also stopped equilibrating with the nebular gas at higher temperatures than those that contributed noble metals to the latter. Murchison inclusions tend to be lower in non-refractory elements than Allende coarse-grained inclusions, suggesting that, on average, the former underwent less severe secondary alteration than the latter.     

Ordered mixed-layer structures in the Mighei carbonaceous chondrite matrix

High resolution transmission electron microscopy of the Mighei carbonaceous chondrite matrix has revealed the presence of a new mixed layer structure material. This mixed-layer material consists of an ordered arrangement of serpentine-type (S) and brucite-type (B) layers in the sequence … SBBSBB. … Electron diffraction and imaging techniques show that the basal periodicity is ~ 17 Å. Discrete crystals of SBB-type material are typically curved, of small size (<1 μm) and show structural variations similar to the serpentine group minerals. Mixed-layer material also occurs in association with planar serpentine. Characteristics of SBB-type material are not consistent with known terrestrial mixed-layer clay minerals. Evidence for formation by a condensation event or by subsequent alteration of preexisting material is not yet apparent.     

Isotopic lead investigations on the Allende carbonaceous chondrite

Uranium and lead concentrations and the isotopic compositions of lead were determined on samples of total rock, matrix, white inclusion, pink inclusion, white aggregate and four chondrules from the Allende carbonaceous chondrite. Observed ²⁰⁶Pb/²⁰⁴Pb ratios varied from 10.004 to 107.29; ²⁰⁷Pb/²⁰⁴Pb ratios from 10.695 to 69.07; ²⁰⁶Pb/²⁰⁴Pb ratios from 30.062 to 207.96. In a ²⁰⁷Pb/²⁰⁴Pb-²⁰⁶Pb/²⁰⁴Pb diagram a regression line fitted to all of data has a slope of 0.6240 ± 0.0015, corresponding to a single stage model age of 4.565 ± 0.004 AE. The regression line also includes the ratios for primordial lead as determined in previous investigations from Canyon Diablo troilite and the Mezö-Madaras chondrite.Although the lead in the matrix is not very radiogenic, the ²⁰⁷Pb/²⁰⁶Pb ages of four samples average 4.505 AE, a value 0.06 AE younger than that of the chondrules and inclusions. The matrix age agrees closely with a total rock Pb/Pb model age previously reported for Allende by Tatsumoto, Knight and Allegre. The matrix Pb/Pb model age is also 0.06 AE younger than the Pb/Pb isochron ages determined by previous investigators on total samples of H and L chondrites. The H and L chondrite and Allende chondrule and inclusion Pb/Pb ages are indistinguishable. The lead isotope systematics require either that the matrix is ca. 0.06 younger than the silicate inclusions and chondrules (or that radiogenic lead was inherited from a younger external source) or that the initial lead in the matrix differed from primordial lead. The lead data cannot be reconciled to a model in which the bulk material of Allende first crystallized 4.57 AE ago, followed by transfer of radiogenic lead between phases since that time.In a concordia diagram four chondrules and three inclusions plot along a chord intersecting concordia at 4.57 and 0.28 ± 0.07 AE. This indicates disturbance of the U-Pb systems relatively recently, perhaps around 0.3 AE ago. The time of disturbance is not readily understood and needs further confirmation. It correlates most closely with a possible cut-off in K-Ar and U, Th-He ages of chondrites.Although the Th/U ratios of the bulk samples and matrix are around the normal value of 3.8, much higher values are observed in some of the inclusions, the highest being 9.0.     

Extremely Na- and Cl-rich chondrule from the CV3 carbonaceous chondrite Allende

We report on a study of Al3509, a large Na- and Cl-rich, radially-zoned object from the oxidized CV carbonaceous chondrite Allende. Al3509 consists of fine-grained ferroan olivine, ferroan Al-diopside, nepheline, sodalite, and andradite, and is crosscut by numerous veins of nepheline, sodalite, and ferroan Al-diopside. Some poorly-characterized phases of fine-grained material are also present; these phases contain no significant H₂O. The minerals listed above are commonly found in Allende CAIs and chondrules and are attributed to late-stage iron-alkali-halogen metasomatic alteration of primary high-temperature minerals. Textural observations indicate that Al3509 is an igneous object. However, no residual crystals that might be relicts of pre-existing CAI or chondrule minerals were identified. To establish the levels of ²⁶Al and ³⁶Cl originally present, ²⁶Al-²⁶Mg and ³⁶Cl-³⁶S isotopic systematics in sodalite were investigated. Al3509 shows no evidence of radiogenic ²⁶Mg^∗, establishing an upper limit of the initial ²⁶Al/²⁷Al ratio of 3 × 10⁻⁶. All sodalite grains measured show large but variable excesses of ³⁶S, which, however, do not correlate with ³⁵Cl/³⁴S ratio. If these excesses are due to decay of ³⁶Cl, local redistribution of radiogenic ³⁶S^∗ after ³⁶Cl had decayed is required. The oxygen-isotope pattern in Al3509 is the same as found in secondary minerals resulting from iron-alkali-halogen metasomatic alteration of Allende CAIs and chondrules and in melilite and anorthite of most CAIs in Allende. The oxygen-isotope data suggest that the secondary minerals precipitated from or equilibrated with a fluid of similar oxygen-isotope composition. These observations suggest that the formation of Al3509 and alteration products in CAIs and chondrules in Allende requires a very similar fluid phase, greatly enriched in volatiles (e.g., Na and Cl) and with Δ¹⁷O ∼ −3‰. We infer that internal heating of planetesimals by ²⁶Al would efficiently transfer volatiles to their outer portions and enhance the formation of volatile-enriched minerals there. We conclude that the site for the production of Na- and Cl-rich fluids responsible for the formation of Al3509 and the alteration of the Allende CAIs and chondrules must have been on a protoplanetary body prior to incorporation into the Allende meteorite. Galactic cosmic rays cannot be the source of the inferred initial ³⁶Cl in Allende. The problem of ³⁶Cl production by solar energetic particle (SEP) bombardment and the possibility that ³⁶Cl and ⁴¹Ca might be the product of neutron capture resulting from SEP bombardment of protoplanetary surfaces are discussed. This hypothesis can be tested comparing inferred “initial” ³⁶Cl with neutron fluencies measured on the same samples and on phases showing ³⁶S^∗ by Sm and Gd isotopic measurements.     

Isotopic anomalies in organic nanoglobules from Comet 81P/Wild 2: Comparison to Murchison nanoglobules and isotopic anomalies induced in terrestrial organics by electron irradiation

Nanoglobules are a form of organic matter found in interplanetary dust particles and primitive meteorites and are commonly associated with ¹⁵N and D isotopic anomalies that are suggestive of interstellar processes. We report the discovery of two isotopically-anomalous organic globules from the Stardust collection of particles from Comet 81P/Wild 2 and compare them with nanoglobules from the Murchison CM2 meteorite. One globule from Stardust Cometary Track 80 contains highly aromatic organic matter and a large ¹⁵N anomaly (δ¹⁵N = 1120‰). Associated, non-globular, organic matter from this track is less enriched in ¹⁵N and contains a mixture of aromatic and oxidized carbon similar to bulk insoluble organic material (IOM) from primitive meteorites. The second globule, from Cometary Track 2, contains non-aromatic organic matter with abundant nitrile (CN) and carboxyl (COOH) functional groups. It is significantly enriched in D (δD = 1000‰) but has a terrestrial ¹⁵N/¹⁴N ratio. Experiments indicate that similar D enrichments, unaccompanied by ¹⁵N fractionation, can be reproduced in the laboratory by electron irradiation of epoxy or cyanoacrylate. Thus, a terrestrial origin for this globule cannot be ruled out, and, conversely, exposure to high-energy electron irradiation in space may be an important factor in producing D anomalies in organic materials. For comparison, we report two Murchison globules: one with a large ¹⁵N enrichment and highly aromatic chemistry analogous to the Track 80 globule and the other only moderately enriched in ¹⁵N with IOM-like chemistry. The observation of organic globules in Comet 81P/Wild 2 indicates that comets likely sampled the same reservoirs of organic matter as did the chondrite parent bodies. The observed isotopic anomalies in the globules are most likely preserved signatures of low temperature (<10 K) chemistry in the interstellar medium or perhaps the outer regions of the solar nebula. In other extraterrestrial samples, D isotopic anomalies, but not those of ¹⁵N, may be explained in part by exposure to ionizing electron radiation.     

Evidence for aqueous alteration in a carbonaceous xenolith from the Plainview (H5) chondrite

Within a CM-like clast in the Plainview (H5) chondrite are two inclusions which have the distinctive morphologies of an Allende-like, coarse-grained CAI and an amoeboid olivine inclusion respectively. The compositions of the mineral components within the inclusions were ascertained in this microprobe study. The major constituents of the altered inclusions are calcite, Mg-Fe-rich phyllosilicates, Fe-Ti oxides, and an unusually Al-rich (21–32 wt% A1₂O₃) phyllosilicate. Assuming the starting compositions for these inclusions suggested by their morphologies, namely, Ca-Al refractory-rich oxides and silicates, the alteration process would have required transport of Na, Cl, H₂O, “CO₂” and “FeO”. Because significant quantities of iron are required to produce the mineral assemblages now present from the inferred starting materials, and because of the presence of hydrous phases, it seems that liquid water was probably the medium in which the alteration reactions took place. The two possible sources of liquid water in meteorite parent bodies are primordially formed clay minerals and water ice. As yet neither source can be ruled out.     

The isotopic composition of carbonaceous matter in a metamorphic profile from the Swiss Alps

44 Δ¹³C-values for carbonaceous matter in a metamorphic profile from the Swiss Alps have been determined. The analyzed samples range from unmetamorphosed sediments to staurolite schists. The carbon isotopic composition is more-or-less constant with δ-values around ?25%. in the unmetamorphosed sediments, but shifts towards higher ¹³C-content with increasing grade of metamorphism. δ¹³C values of around ?11%. were measured in the rocks of the highest metamorphic grade.     

The oxygen-isotope composition of chondrules and isolated forsterite and olivine grains from the Tagish Lake carbonaceous chondrite

The oxygen-isotope compositions (obtained by laser fluorination) of hand-picked separates of isolated forsterite, isolated olivine and chondrules from the Tagish Lake carbonaceous chondrite describe a line (δ¹⁷O = 0.95 * δ¹⁸O − 3.24; R² = 0.99) similar to the trend known for chondrules from other carbonaceous chondrites. The isolated forsterite grains (Fo_99.6-99.8; δ¹⁸O = −7.2‰ to −5.5‰; δ¹⁷O = −9.6‰ to −8.2‰) are more ¹⁶O-rich than the isolated olivine grains (Fo_39.6-86.8; δ¹⁸O = 3.1‰ to 5.1‰; δ¹⁷O = −0.3‰ to 2.2‰), and have chemical and isotopic characteristics typical of refractory forsterite. Chondrules contain olivine (Fo_97.2-99.8) with oxygen-isotope compositions (δ¹⁸O = −5.2‰ to 5.9‰; δ¹⁷O = −8.1‰ to 1.2‰) that overlap those of isolated forsterite and isolated olivine. An inverse relationship exists between the Δ¹⁷O values and Fo contents of Tagish Lake isolated forsterite and chondrules; the chondrules likely underwent greater exchange with ¹⁶O-poor nebular gases than the forsterite. The oxygen-isotope compositions of the isolated olivine grains describe a trend with a steeper slope (1.1 ± 0.1, R² = 0.94) than the carbonaceous chondrite anhydrous mineral line (CCAM_slope = 0.95). The isolated olivine may have crystallized from an evolving melt that exchanged with ¹⁶O-poor gases of somewhat different composition than those which affected the chondrules and isolated forsterite. The primordial components of the Tagish Lake meteorite formed under conditions similar to other carbonaceous chondrite meteorite groups, especially CMs. Its alteration history has its closest affinities to CI carbonaceous chondrites.     

Molecular and compound-specific hydrogen isotope analyses of insoluble organic matter from different carbonaceous chondrite groups

We have conducted the first systematic analyses of molecular distribution and δD values of individual compounds in pyrolysates of insoluble organic matter (IOM) from different carbonaceous chondrite groups, using flash pyrolysis coupled to gas chromatography-mass spectrometry and compound-specific D/H analysis. IOM samples from six meteorites of different classifications, Elephant Moraine (EET) 92042 (CR2), Orgueil (CI1), Allan Hills (ALH) 83100 (CM1/2), Murchison (CM2), ALH 85013 (CM2), and Tagish Lake (C2) were isolated and studied. Except for the pyrolysate of Tagish Lake IOM, pyrolysates of all five meteorite IOM samples were dominated by an extensive series of aromatic (C₁ to C₇ alkyl-substituted benzenes, C₀ to C₂ alkyl-substituted naphthalenes), with aliphatic (straight chain and branched C₁₀ to C₁₅ alkanes) hydrocarbons and several S- and O- containing compounds (C₁ to C₂ alkylthiophenes, benzothiophene, benzaldehyde) being also present. The strong similarity in the pyrolysates of different carbonaceous chondrites suggests certain common characteristics in the formation mechanisms of IOM from different meteorites. The Tagish Lake IOM sample is unique in that its pyrolysate lacks most of the alkyl-substituted aromatic hydrocarbons detected in other meteorite IOM samples, suggesting distinctively different formation processes. Both bulk δD values of meteorite IOMs and weighted-average δD values of individual compounds in pyrolysates show a decreasing trend: CR2 > CI1 > CM2 > C2 (Tagish Lake), with the EET 92042 (CR2) IOM having the highest δD values (∼2000‰ higher than other samples). We attribute the high D contents in the IOM to primitive interstellar organic sources.