A carbon and nitrogen isotope study of diamond from primitive chondrites

Abstract Diamonds isolated from primitive chondrites of the carbonaceous, ordinary and enstatite groups have been analysed by high-resolution stepped combustion, followed by measurement of their C and N isotopes using a newly adapted technique that allows quantitative measurements of C/N ratios. The δ¹³C of the diamond is shown to vary between meteorite groups from ?32 to ?38%0, and the measured C/N ratios suggest that the N concentration of diamond ranges over a factor of 7 from 1800 ppm (Tieschitz) to 13,000 ppm (Adrar 003). The δ¹⁵N of N released from diamond is constrained to ?348 ± 7%. The complexity of the C release pattern and C/N ratio during combustion implies the presence of more than one component, which suggests that either more than one type of diamond is present in the samples, or unidentified additional phases are located in the acid-resistant residue. The components are present in varying proportions between meteorite groups. The data are compatible with a model of a mix of different diamond populations (some probably presolar and some possibly solar) existing in the early solar nebula, where each population originally contributed a roughly equal amount to chondrites of every class. Subsequent metamorphism has resulted in overall variations in δ¹³C and C/N ratios in diamond isolated from meteorites of differing petrologic grade without significantly altering the N isotopic composition. Possible ways for this to be achieved are explored.     

A New Martian Meteorite: the Dhofar 019 Shergottite with an Exposure Age of 20 Million Years

The isotopic composition of the noble gases of the new Martian meteorite, the Dhofar 019 shergottite, found in the desert in the territory of the Sultanate of Oman on January 24, 2001, was investigated. Stepwise thermal annealing with isotopic analysis of each of the noble-gas temperature fractions was employed to determine the component composition. The concentration of the trapped noble gases in the new Martian meteorite Dhofar 019 is relatively high, although it lies within the range of concentrations in known SNC meteorites. A characteristic feature of all the trapped noble gases is the presence of two main components: a low-temperature, probably terrestrial atmospheric, component, trapped during the weathering of the meteorite on Earth, and a high-temperature trapped Martian component. Owing to the different ratios of the quantities of the two components, the trapped neon, argon, krypton, and xenon differ markedly in the kinetics of their release. The isotopic composition of the noble gases varies accordingly. The trapped xenon was found to contain two Martian components. One of them, with typical ratios of ¹²⁹Xe/¹³²Xe and ¹³²Xe/⁸⁴Kr, is representative of xenon and krypton of the Martian atmosphere; the other, of gases of the Martian mantle. Variations of the isotopic compositions of helium, neon, and argon (and also, to a lesser extent, of krypton and xenon) during the thermal annealing of the Dhofar 019 meteorite clearly point to a large proportion of cosmogenic as well as trapped components. The concentration of cosmogenic neon and argon in the meteorite is unusually high. This corresponds to a maximum exposure age among other SNC meteorites: 20 million years. Estimates of the potassium–argon age (gas-retention age) yielded the figure of 560 million years, which is within the range of values obtained for SNC meteorites by other authors, who used the rubidium–strontium and the potassium–argon technique.     

The oxygen isotopic composition of water from Tagish Lake: Its relationship to low‐temperature phases and to other carbonaceous chondrites

Abstract— The fall and recovery of the Tagish Lake meteorite in British Columbia in January 2000 provided a unique opportunity to study relatively pristine samples of carbonaceous chondrite material. Measurements of the oxygen isotopic composition of water extracted under stepped pyrolysis from a bulk sample of this meteorite have allowed us to make comparisons with similar data obtained from CI and CM chondrites and so further investigate any relationships that may exist between these meteorites. The much lower yield of water bearing a terrestrial signature in Tagish Lake is indicative of the pristine nature of the meteorite. The relationship between the isotopic composition of this water and reported isotopic values for carbonates, bulk matrix and whole rock have been used to infer the extent and conditions under which parent‐body aqueous alteration occurred. In Tagish Lake the difference in Δ17O isotopic composition between the water and other phases is greater than that found in either CM or CI chondrites suggesting that reaction and isotopic exchange between components was more limited. This in turn suggests that in the case of Tagish Lake conditions during the processes of aqueous alteration on the parent body, which ultimately controlled the formation of new minerals, were distinct from those on both CI and CM parent bodies.     

Nitrogen‐isotopic compositions of IIIE iron meteorites

Abstract— The (compositionally) closely related iron meteorite groups IIIE and IIIAB were originally separated based on differences in kamacite bandwidth, the presence of carbides only in the IIIE group, and marginally resolvable differences on the Ga‐Ni and Ge‐Ni diagrams. A total of six IIIE iron meteorites have been analyzed for C and N using secondary ion mass spectrometry, and three of these have also been analyzed for N, Ne, and Ar by stepped combustion. We show that these groups cannot be resolved on the basis of N abundances or isotopic compositions but that they are marginally different in C‐isotopic composition and nitride occurrence. Cosmic‐ray exposure age distributions of the IIIE and IIIAB iron meteorites seem to be significantly different. There is a significant N‐isotopic range among the IIIE iron meteorites. A negative correlation between δ15N and N concentration suggests that the increase in s?15N resulted from diffusional loss of N.     

Kinetics of Xe‐P3 release during pyrolysis of the coarse‐grained fractions of Orgueil (CI) meteorite nanodiamonds

The kinetics of the release of the Xe‐P3 component from coarse‐grained fractions of Orgueil (CI) meteorite nanodiamonds has been investigated using stepped and isothermal pyrolysis. It has been shown that a first‐order chemical reaction diffusion model with a single activation energy cannot provide a satisfactory explanation for the observed retention of Xe‐P3 during parent body thermal metamorphism and the kinetics of Xe‐P3 release from nanodiamonds during isothermal pyrolysis. Using the activation energy and frequency factor calculated according to this model, it is shown that in the course of thermal metamorphism of the Orgueil meteorite almost the entire Xe‐P3 component must have been lost in a very short time (<4 yr at approximately 100 °C). However, the calculated retention of Xe‐P3 increases significantly if a diffusion model with a spectrum of activation energies is used. In this case, the model can explain not only a high retention of Xe‐P3 in the Orgueil nanodiamonds but also the release pattern of the Xe‐P3 from Semarkona and Bishunpur nanodiamonds that have experienced a significant gas loss during parent body metamorphism as well as the release of Xe‐P3 during isothermal pyrolysis of the Orgueil nanodiamonds. The energetically complicated Xe‐P3 distribution is most likely caused by structural damage to the nanodiamond grains or a complex phase composition of carbon in the surface layer of the diamond grains. It is supposed that the structural damage of the diamond grains can have a radiation origin, while the variations of the carbon phase composition in the grain's mantle can be caused by the radiation‐induced reactions and/or a thermal effect.     

Carbon isotopic composition of acetic acid generated by hydrous pyrolysis of macromolecular organic matter from the Murchison meteorite

Abstract— Low molecular weight monocarboxylic acids, including acetic acid, are some of the most abundant organic compounds in carbonaceous chondrites. So far, the ¹³C‐ and D‐enriched signature of water‐extractable carboxylic acids has implied an interstellar contribution to their origin. However, it also has been proposed that monocarboxylic acids could be formed by aqueous reaction on the meteorite parent body. In this study, we conducted hydrous pyrolysis of macromolecular organic matter purified from the Murchison meteorite (CM2) to examine the generation of monocarboxylic acids with their stable carbon isotope measurement. During hydrous pyrolysis of macromolecular organic matter at 270–330 °C, monocarboxylic acids with carbon numbers ranging from 2 (C₂) to 5 (C₅) were detected, acetic acid (CH₃COOH; C₂) being the most abundant. The concentration of the generated acetic acid increased with increasing reaction temperature; up to 0.48 mmol acetic acid/g macromolecular organic matter at 330 °C. This result indicates that the Murchison macromolecule has a potential to generate at least ?0.4 mg acetic acid/g meteorite, which is about four times higher than the amount of water‐extractable acetic acid reported from Murchison. The carbon isotopic composition of acetic acid generated by hydrous pyrolysis of macromolecular organic matter is ?‐27‰ (versus PDB), which is much more depleted in ¹³C than the water‐extractable acetic acid reported from Murchison. Intramolecular carbon isotope distribution shows that methyl (CH₃‐)‐C is more enriched in ¹³C relative to carboxyl (‐COOH)‐C, indicating a kinetic process for this formation. Although the experimental condition of this study (i.e., 270–330 °C for 72 h) may not simulate a reaction condition on parent bodies of carbonaceous chondrite, it may be possible to generate monocarboxylic acids at lower temperatures for a longer period of time.     

Carbon Stable Isotope Analyses of Individual Deep-Sea Spherules

Abstract— A preliminary investigation into the carbon isotopic composition of deep-sea spherules has been undertaken. A variety of particles have been analysed including both melted and unmelted samples of type S (stony) and type I (iron) spherules, emphasis being placed on surveying the carbon in different sorts of particles rather than analysing large numbers of samples. Some general observations can be made: there appear to be four different sorts of carbonaceous materials in the spherules. Melted and unmelted spherules of either type I or S, apparently contain two forms of low temperature combustible carbon distinguished, not by combustion temperature, but by isotopic composition. The low temperature of combustion is commensurate with these forms of carbon being organic in nature. The most likely explanation for this carbon is terrestrial biogenic contamination although there exists the possibility that there are some indigenous organic materials. Unmelted type S spherules contain a high temperature carbon component, characterised by a very minor ¹³C-enrichment, which is considered to be indigenous to the sample. All melted samples contain only small amounts of high temperature carbon with an isotopic composition suggestive of handling blank.     

THE ISOTOPIC COMPOSITION OF TELLURIUM IN THE ABEE METEORITE

Smith et al. (1978) measured the isotopic composition of tellurium in a number of whole rock meteorites by solid source spectrometry and concluded that all the data were identical to a terrestrial standard within experimental errors. However, Oliver et al. (1981) reexamined the data reported by Smith et al. (1978) and argued that, in the case of the Abee meteorite, a negative anomaly in ¹²⁴Te may be present, supporting the claim for a similar anomaly in Allende. The present work reports two sets of measurements of the tellurium isotopic composition of Abee, and compares the meteoritic data with a terrestrial tellurium standard. No isotopic anomalies can be distinguished within the error limits. However, further work on the isotopic composition of Te in residues from the Allende meteorite need to be pursued by accurate mass spectrometric analysis.     

Search for solar-type nitrogen in the gas-rich Pesyanoe meteorite

Abstract— We report nitrogen isotopic data obtained from a stepwise gas release of two grain-size fractions of the gas-rich meteorite Pesyanoe. Cosmic-ray-produced ¹⁵N_c may be present in all temperature steps ≥600 °C, and we correct this component using spallation ²¹Ne data. The resulting ratios reveal the presence of more than one trapped N component. Indigenous N is released above 1000 °C with an isotopic signature of δ¹⁵N = ?33‰. This is consistent with the rather uniform signatures of indigenous nitrogen in enstatite meteorites. There is no evidence for the presence of “very light” N of δ¹⁵N ? ?200‰. On the other hand, a “heavy” nitrogen component appears in the temperature range 700–800 °C, and coincides with a major release of solar-type noble gases. For a two-component mixture, the isotopic shifts in this temperature range define a lower limit δ¹⁵N_corr = ?6‰ for the second component (e.g., solar-type nitrogen). However, for the case of a solar-type component, the calculated δ¹⁵N signature depends on the adopted elemental abundances. For example, adoption of the relative abundances of ¹⁴N and noble gases in lunar ilmenite 71501 yields δ¹⁵N ? +170, which is in the range of the heavier nitrogen signatures observed on the lunar surface.     

Potassium isotopic compositions of enstatite meteorites

Enstatite chondrites and aubrites are meteorites that show the closest similarities to the Earth in many isotope systems that undergo mass‐independent and mass‐dependent isotopic fractionations. Due to the analytical challenges to obtain high‐precision K isotopic compositions in the past, potential differences in K isotopic compositions between enstatite meteorites and the Earth remained uncertain. We report the first high‐precision K isotopic compositions of eight enstatite chondrites and four aubrites and find that there is a significant variation of K isotopic compositions among enstatite meteorites (from ?2.34‰ to ?0.18‰). However, K isotopic compositions of nearly all enstatite meteorites scatter around the bulk silicate earth (BSE) value. The average K isotopic composition of the eight enstatite chondrites (?0.47 ± 0.57‰) is indistinguishable from the BSE value (?0.48 ± 0.03‰), thus further corroborating the isotopic similarity between Earth's building blocks and enstatite meteorite precursors. We found no correlation of K isotopic compositions with the chemical groups, petrological types, shock degrees, and terrestrial weathering conditions; however, the variation of K isotopes among enstatite meteorite can be attributed to the parent‐body processing. Our sample of the main‐group aubrite MIL 13004 is exceptional and has an extremely light K isotopic composition (δ⁴¹K = ?2.34 ± 0.12‰). We attribute this unique K isotopic feature to the presence of abundant djerfisherite inclusions in our sample because this K‐bearing sulfide mineral is predicted to be enriched in ³⁹K during equilibrium exchange with silicates.     

Abundance and isotopic composition of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite

Abstract— Abundances and isotopic compositions of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite were measured. The abundance ratios of spallogenic components in metal reveal a ³He deficiency which is due to the diffusive loss of parent isotopes, that is, tritium (Tilles, 1963; Schultz, 1967). The diffusive loss likely has been induced by thermal heating by the Sun during cosmic‐ray exposure (～160 Ma; Lavielle et al, 1999). Thermal process such as impact‐induced partial loss may have affected the isotopic composition of spallogenic Ne. The ¹²⁹Xe/¹³¹Xe ratio of cosmogenic components in the metal indicates an enhanced production of epi‐thermal neutrons. The abundance ratios of spallogenic components in the graphite reveal that it contained small amounts of metal and silicates. The isotopic composition of heavy noble gases in graphite itself was obtained from graphite treated with HF/HCl. The isotopic composition of the etched graphite shows that it contains two types of primordial Xe (i.e., Q‐Xe and El Taco Xe). The isotopic heterogeneity preserved in the Bohumilitz graphite indicates that the Bohumilitz graphite did not experience any high‐temperature event and, consequently, must have been emplaced into the metal at subsolidus temperatures. This situation is incompatible with an igneous model as well as the impact melting models for the IAB‐IIICD iron meteorites as proposed by Choi et al. (1995) and Wasson et al (1980).     

Determination of sulphur-bearing components in C1 and C2 carbonaceous chondrites by stepped combustion

Abstract— Ten type 1 and 2 carbonaceous chondrites have been analysed by stepped combustion to determine the nature of their sulphur-bearing components. All samples show complex release patterns which, when combined with published petrographic observations, can be interpreted in terms of sulphur derived from a mixture of at least seven components (elemental sulphur, organic sulphur, sulphide, FESON or tochilinite and sulphates: gypsum, bloedite and epsomite). Estimated concentrations of individual components show that most of the sulphur in the meteorites exists in oxidised form. The concentrations of reduced and oxidised components can be used to derive approximate oxidised/reduced sulphur ratios for the meteorites. These ratios are indicators of the extent of aqueous alteration and increase in the order CM < CI. Formation of the different alteration products by aqueous processes active on the meteorite parent body appears to be the most likely origin.     

Presolar silicon carbide from the Indarch (EH4) meteorite: Comparison with silicon carbide populations from other meteorite classes

Abstract— Presolar SiC from the Indarch (EH4) meteorite was studied by scanning electron microscopy (SEM), by ion probe analysis for C and Si isotopic compositions, and by static source mass spectrometry for noble gas and C isotopic compositions. The data obtained are compared to SiC data from other meteorites, especially from Murchison (CM2), for which there is the most information available. The isotopic compositions of the major elements in SiC from Indarch and Murchison are similar. Stepped combustion data suggest a mean δ¹³C for SiC from both meteorites of ～+1430%o. Silicon isotopes in Indarch and Murchison SiC also compare well. In some other important respects, however, SiC in the two meteorites are different. Morphologically, SiC from Indarch appears finer grained than SiC from Murchison and is entirely composed of submicron grains. The finer-grained nature of Indarch SiC is confirmed by its noble gas characteristics. The mean Ne-E/Xe-S ratio for bulk Indarch SiC is significantly lower than the same ratio in Murchison (625 ± 47 vs. ～3500) but is similar to that of the finest grain-size fractions (<1 μm) in Murchison. A comparison of noble gas data from SiC from several different meteorites suggests that it might be Murchison SiC, rather than Indarch SiC, that is unusual. The grain-size disparities in SiC between meteorites are difficult to explain by residue processing differences or differing parent body processing. Instead, we speculate that a grain-size sorting mechanism for SiC may have operated in the solar nebula.     

A review of volatile compounds in tektites,and carbon content and isotopic composition of moldavite glass

Abstract– Tektites, natural silica‐rich glasses produced during impact events, commonly contain bubbles. The paper reviews published data on pressure and composition of a gas phase contained in the tektite bubbles and data on other volatile compounds which can be released from tektites by either high‐temperature melting or by crushing or milling under vacuum. Gas extraction from tektites using high‐temperature melting generally produced higher gas yield and different gas composition than the low‐temperature extraction using crushing or milling under vacuum. The high‐temperature extraction obviously releases volatiles not only from the bubbles, but also volatile compounds contained directly in the glass. Moreover, the gas composition can be modified by reactions between the released gases and the glass melt. Published data indicate that besides CO₂ and/or CO in the bubbles, another carbon reservoir is present directly in the tektite glass. To clarify the problem of carbon content and carbon isotopic composition of the tektite glass, three samples from the Central European tektite strewn field—moldavites—were analyzed. The samples contained only 35–41 ppm C with δ¹³C values in the range from ?28.5 to ?29.9‰ VPDB. This indicates that terrestrial organic matter was a dominant carbon source during moldavite formation.     

Noble gas measurements in the L/LL5 chondrite Knyahinya

Abstract— The L/LL5 chondrite Knyahinya had an approximately spherical shape, and as it experienced a single stage exposure history, it represents a very interesting object to study depth profiles of cosmic-ray-produced nuclide concentrations. Such data are required to improve and to validate model calculations of production rates. We report Ne, Ar, Kr and Xe isotopic abundances in five bulk samples. The adopted procedure of noble gas extraction included two pyrolysis steps at 450 °C and 650 °C, respectively, followed by a combustion step in pure O₂ at 650 °C before melting the sample. This procedure allows for the separation of a significant fraction of the trapped Kr and Xe, leading to an enrichment of the cosmic-ray produced component, which is released in the melting step. The isotopic composition of the trapped Xe component measured in the combustion step is found to be identical with the OC-Xe composition (Lavielle and Marti, 1992) and supports the suggestion that ordinary chondrites formed in a homogeneous trapped noble gas reservoir. Cosmic-ray produced Kr and Xe components and depth profiles were measured, including for the first time a ⁸¹Kr profile. The calculated exposure age of 39.5 ± 1.0 Ma, based on the ⁸¹Kr-Kr method, is found to be in excellent agreement with previous determinations. The concentrations of trapped and fissiogenic noble gas components are clearly lower than those generally observed in type 5 ordinary chondrites and may suggest diffusion losses before a meter-sized object was exposed to the cosmic radiation.     

Thuathe,a new H4/5 chondrite from Lesotho: History of the fall,petrography, and geochemistry

Abstract— On July 21, 2002, a meteorite fall occurred over the Thuathe plateau of western Lesotho. The well‐defined strewn field covers an area of 1.9 times 7.4 km. Many of the recovered specimens display a brecciated texture with leucocratic, angular to subrounded clasts in a somewhat darker groundmass. Mineralogical and chemical data, as well as oxygen isotopic analysis, indicate that Thuathe is an H4/5, S2/3 meteorite, with local H3 or H6 character. A number of anomalous features include somewhat high Co contents of kamacite and taenite relative to normal H‐group chondrites. Oxygen isotopic data plot at the edge of the normal H chondrite data field. Variable contents of metallic mineral phases and troilite result in a heterogeneous bulk composition (e.g., with regard to Si, Fe, and Mg), resulting in a spread of major element ratios that is not consistent with previously accepted H‐group composition. Trace element abundances are generally consistent with H chondritic composition, and Kr and Xe isotopic data agree with an H4 classification for this meteorite. Noble gas analysis gave U, Th‐⁴He gas retention and K‐Ar ages typical for H chondrites; no major thermal event affected this material since ～3.7 Ga. The exposure age for Thuathe is 5 Ma, somewhat lower than for other H chondrites. Cosmogenic nuclide analysis indicates a pre‐atmospheric radius of this meteorite between 35 and 40 cm. In the absence of evidence for solar gases, we classify Thuathe as a fragmental breccia. Numerous narrow, black veins cut across samples of Thuathe and are the result of a brittle deformation event that also caused local melting, especially in portions rich in sulfide. The formation of these veinlets is not the result of locally enhanced shock pressures (i.e., of shock melting) but rather of shearing under brittle conditions with local, friction‐related temperature excursions causing melting mostly of Fe‐sulfide and FeNi‐metal but also, locally, of silicate minerals. Frictional temperature excursions must have attained values in excess of 1500 °C to permit complete melting of forsteritic olivine.     

Isotope fractionation and concentration measurements of Zn in meteorites determined by the double spike,IDMS‐TIMS techniques

Abstract– The isotope fractionation of Zn in meteorites has been measured for the first time using thermal ionization mass spectrometry and a double spiking technique. The magnitude of δZn ranged from ?0.29 to +0.38‰ amu^?1 for five stone meteorites whereas the iron meteorite Canyon Diablo displays δZn of 1.11 ± 0.11‰ amu^?1. The results for chondrites in this work can be divided into positive and negative δZn, supporting a previous proposal that chondrites are a mixture of materials from two different temperature sources. The Zn isotope fractionation present in meteorites may represent a primordial heterogeneity formed in the early solar system. An anomalous isotopic composition of Zn obtained for the Redfields iron meteorite suggests large‐scale inherited isotope heterogeneity of the protosolar nebula, or the presence of a parent body that has formed within its own isotopically anomalous reservoir. These anomalies are in the same direction but smaller than nuclear field shift effects observed in chemical exchange reactions. The isotope dilution mass spectrometry (IDMS) technique was used to measure Zn concentration, yielding a range from 20.1 μg g^?1 to 302 μg g^?1 in five stone meteorites and from 0.019 to 26 μg g^?1 in seven iron meteorites. The IDMS‐measured abundance of Zn in Orgueil is 302 ± 14 μg g^?1 and should be considered for future compilations of the abundance of Zn in the solar system.     

On unfractionated solar noble gases in the H3–6 meteorite Acfer 111

Abstract Solar noble gases He, Ne, Ar and Kr implanted in the H3–6 meteorite regolith breccia Acfer 111 agree in their elemental composition with that in present-day solar wind and, except for a 25% deficit of ⁴He, also with adopted solar abundances. The presence of such unfractionated solar gases makes Acfer 111 unique (until now). Closed system stepped etching releases noble gases that can be explained as mixtures of two distinct types of He, Ne, and Kr of isotopic compositions as they have been derived previously from meteorites and lunar samples that contain heavily fractionated solar gases. Since the same putative end members, ascribed to the solar wind (SW) and supra-thermal solar energetic particles (SEP), are also present in Acfer 111, we argue that these end members represent two truly independent components. We discount the possibility that one isotopic composition derived from the other by diffusion of the gases within, or upon their release from, their host phases. The isotopic signatures of noble gases in Acfer 111 agree with those in a lunar ilmenite of young antiquity ?100 Ma) but are in disagreement with the noble gases in lunar ilmenite 79035 of 1–2 Ga antiquity. Systematic changes are discussed of the nuclide abundance ratios as etching proceeds; they are ascribed to differences in trapping efficiency and in penetration depth of the different noble gas ion species upon their implantation.     

Molecular and isotopic analyses of Tagish Lake alkyl dicarboxylic acids

Abstract— The Tagish Lake meteorite soluble organic suite has a general composition that differs from those of both CI and CM chondrites. These differences suggest that distinct processes may have been involved in the formation of different groups of organics in meteorites. Tagish Lake alkyl dicarboxylic acids have a varied, abundant distribution and are, with carboxylated pyridines, the only compounds to have an occurrence comparable to that of the Murchison meteorite. This study has undertaken their molecular and isotopic characterization, with the aim to understand their origin and to gain insights into the evolutionary history of the meteorite parent body. Tagish Lake alkyl dicarboxylic acids are present as a homologous series of saturated and unsaturated species with three‐ through ten‐carbon atom chain length. Linear saturated acids are predominant and show decreasing amounts with increasing chain length. A total of 44 of these compounds were detected with the most abundant, succinic acid, present at ?40 nmol/g meteorite. Overall the molecular distribution of Tagish Lake dicarboxylic acids shows a remarkable compound‐to‐compound correspondence with those observed in the Murchison and Murray meteorites. In both Tagish Lake and Murchison, the imides of the more abundant dicarboxylic acids were also observed. The hydrogen and carbon isotopic compositions of individual Tagish Lake dicarboxylic acids were determined and compared to those of the corresponding acids in the Murchison meteorite. All δD and δ¹³C values for Tagish Lake acids are positive and show a substantial isotopic enrichment. δD values vary from, approximately, +1120%_o for succinic acid to +1530%_o for methyl glutaric acid. δ¹³C values ranged from +12.6%_o for methyl glutaric acid to +22.9%_o for glutaric acid, with adipic acid having a significantly lower value (+5.5%_o). Murchison dicarboxylic acid showed similar isotopic values: their δ5¹³C values were generally higher by an average 17% and δD values were lower for succinic and glutaric acids, possibly due to contamination. The molecular and isotopic data collected for these compounds restrict their possible origin to processes, either interstellar or of very cold nebular regions, that produced significant isotopic enrichments. Saturated or partially unsaturated nitriles and dinitriles appear to be good precursor candidates as their hydrolysis, upon water exposure, would produce dicarboxylic acids and other carboxylated species found in Tagish Lake. This evolutionary course could possibly include pre‐accretionary processes.     

Chemical and isotopic characteristics of the Didwana‐Rajod (H5) chondrite

Abstract— The mineralogical and chemical characteristics of the Didwana‐Rajod chondrite are described. The mean mineral composition is found to be olivine (Fo_83.2) and pyroxene (En_83.5Wo_0.7Fs_15.8), and feldspar is mainly oligoclase. Oxygen isotopic analysis shows δ¹⁸O = +3.8%0 and δ¹⁷O = +2.59%0. The nitrogen content of Didwana‐Rajod is ～2 ppm with δ¹⁵N ? 3.4%0. Based on microscopic, chemical, isotopic and electron probe microanalysis, the meteorite is classified as an H5 chondrite. Cosmogenic tracks, radionuclides and the isotopic composition of rare gases were also measured in this meteorite. The track density in olivines varies in a narrow range with an average value of (6.5 ± 0.5) × 10⁵/cm² for four spot samples taken at the four corners of the stone. The cosmic‐ray exposure age based on neon and argon is 9.8 Ma. ²²Na/²⁶Al ? 0.94 is lower than the solar‐cycle average value of ～1.5 and is consistent with irradiation of the meteoroid to lower galactic cosmic‐ray fluxes as expected at the solar maximum. The track density, rare gas isotopic ratios, ⁶⁰Co activity and other radionuclide data are consistent with a preatmospheric radius of ～15 cm, corresponding to a mass of ～50 kg. The cosmogenic properties are consistent with a simple exposure history in interplanetary space.