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A carbonaceous chondrite from the Antarctic, referred to as the Allan Hills meteorite 77306, appears to be free from terrestrial organic contamination. The presence of both protein and non-protein amino acids and an equal abundance of D- and L-enantiomers of amino acids, is testimony to the extraterrestrial nature of these compounds.
The abundances of some of the straight- and branched-chain isomers of the monocarboxylic acids found in the Murchison carbonaceous chondrite are determined. Monocarboxylic acids extracted from a crushed sample of Murchison interior were quantified by means of gas chromatography and mass spectroscopy after a spiking solution of deuterated analogues of 11 carboxylic acids had been added. Monocarboxylic acid abundances are found to range between 1.83 and 0.01 micromole/g, which is significantly higher than Murchison amino acid concentrations, and to decrease with increasing carbon number for both branched and unbranched molecules. The results are interpreted to support the abiotic extraterrestrial synthesis of monocarboxylic acids. Possible mechanisms leading to the equal synthesis of branched and each unbranched carboxylic acid with the same carbon number are considered, noting that the Fischer-Tropsch Type mechanism by itself is incapable of accounting for the observed distributions.
The surface compositions of Phobos and Deimos as determined by their UV-visible reflectance are compared in order to evaluate the hypothesis that the different surface morphologies of the two satellites are due to different mechanical properties. The UV-visible reflectance spectrum of Deimos is compiled from Mariner 9 UV spectrometry and Canopus star tracker photometry and ground-based colorimetry and polarimetry; the geometric albedo of Deimos is determined from Mariner 9 Canopus star tracker data. The reflectance spectra of Deimos and Phobos are found to be similar in a first approximation, exhibiting low, flat reflectivities in the visible and dropping off sharply in the UV, compatible with a probable carbonaceous chondrite nature for Deimos as well as Phobos and suggesting that their different surface morphologies are most likely due to different orbital histories.
Hydrogen isotopic compositions in seven carbonaceous chondrites lie in the range -70 to +771 per thousand relative to standard mean ocean water. These values decrease, to a range from -145 to +219 per thousand, after low-temperature oxidation in an oxygen plasma. Deuterium enrichment is therefore concentrated in the organic matter, the hydrous silicates probably lying close to the terrestrial range for such material. Calculated values for delta D of the organic fraction are +450 per thousand for Orgueil and Ivuna and up to +1600 per thousand for Renazzo. These enrichments, at least for Orgueil and Ivuna, suggest equilibration with protosolar hydrogen at very low temperatures. Assuming a value of 2.5 x 10 to the -5th for the protosolar D/H ratio, nominal equilibration temperatures of 230 K for silicates and 180 K for organic matter may be derived.
Carbonaceous chondrites of groups CI and CM were formed by impact brecciation and aqueous alteration of earlier generations of mineral phases within the surface regions of two or more parent bodies. Those parent bodies were probably asteroids, rather than comets, although a problem still exists in delivering such material safely to earth. Aqueous activity may have been widespread on asteroids.
Trajectories are calculated of solid carbon particles that spall from a carbonaceous heat shield and travel through a given flow field. The mathematical model takes into account mass, momentum, and energy conservation during evaporation of the particles in an effort to understand spallation phenomena and their consequences in a physical way. The solution technique is applied to available Galileo Probe flow field solutions. Plots of trajectories and other particle parameters are presented for a range of initial particle sizes and velocities. It is shown that a significant amount of gaseous carbon is deposited in the inviscid region and ahead of the bow shock as well as in the ablation layer.
Multiple dust components are considered as a source of the observed anomalies in meteoritic oxygen isotope compositions. It is pointed out that these anomalies are not due to an incomplete mixing of several dust or gas-plus-dust components in the solar nebula. If they were, other elements would display similar anomalies. The anomalies must therefore stem from differing degrees of incomplete exchange of oxygen isotopes between the primordial gas and dust components of the nebula. The dust is more likely to have been the component which was enriched with 0-16. Since the isotopic difference between dust and gas probably could not have been preserved if the dust was ever completely vaporized in the nebula, the Ca,Al-rich inclusions in carbonaceous chondrites are unlikely to be condensates, but instead are distillation residues.
Thus far, organic analysis of carbonaceous chondrites has proven the only fruitful means of examining complex organic matter of extraterrestrial origin. The present paper presents the results of organic analysis of two Antarctic meteorites, Allan Hills (77306) and Yamato (74662), which may be considered free from terrestrial contamination. Ion-exchange chromatography, gas chromatography and mass spectrometery of meteorite samples reveal the presence in Yamato of 15 and in Allan Hills of 20 protein and nonprotein amino acids, the most abundant of which are glycine and alanine. Abundances of the D and L enantiomers of each amino acid are also found to be nearly equal. Data thus indicate an abiotic extraterrestrial origin for the matter, and confirm a lack of terrestrial contamination.
Although thermodynamic calculations predict corundum to be the first condensate from a cooling gas of solar composition, a corundum-hibonite inclusion, BB-5, has for the first time been found in the Murchison carbonaceous chondrite. Ion microprobe measurements of Mg isotopic compositions yield the result, unexpected in such an early condensate, that Mg-26 excesses are small despite large Al-27/Mg-24 ratios. The extreme temperature required to melt this inclusion makes a liquid origin unlikely, except by the hypervelocity impact of refractory bodies. Alternatively, B-5 is a direct gas-solid condensate, and its uniform Mg-26 enrichment must be a characteristic of the reservoir from which it condensed. Nebular heterogeneity in magnesium isotopic composition is the preferred explanation for the formation of such a reservoir.
CCl4 and CH3OH solvent extractions were performed on the Murray, Murchison, Orgueil and Renazzo carbonaceous chondrites. Delta-D values of +300-+500% are found in the case of the CH3OH-soluble organic matter. The combined C, H and N isotope data makes it unlikely that the CH3OH-soluble components are derivable from, or simply related to, the insoluble organic polymer found in the same meteorites. A relation between the event that formed hydrous minerals in CI1 and CM2 meteorites and the introduction of water- and methanol-soluble organic compounds is suggested. Organic matter soluble in CCl4 has no N, and delta-C-13 values are lower than for CH3OH-soluble phases. It is concluded that there either are large isotopic fractionations for carbon and hydrogen between different soluble organic phases, or the less polar components are partially of terrestrial origin.
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 approximately 17 A. Discrete crystals of SBB-type material are typically curved, of small size (less than 1 micron) 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 pre-existing material is not yet apparent.
Stepwise combustion has revealed systematic patterns of isotopic heterogeneity for C, H and N in the insoluble organic fraction (m-kerogen) from the Orgueil and Murray carbonaceous chondrites. Those patterns are essentially identical for both meteorites, indicating a common source of m-kerogen. The data cannot be reconciled with a single mass-fractionation process acting upon a single precursor composition. This indicates either a multi-path history of mass-dependent processing or a significant nucleogenetic contribution, or both. If mass-fractionation were the dominant process, the magnitude of the observed isotopic variability strongly suggests that ion-molecule reactions at very low temperatures, probably in interstellar clouds, were responsible. In any case, an interstellar, rather than solar nebular, origin for at least some of the meteoritic organic matter is indicated. This has interesting implications for the origin of prebiotic molecules, temperatures in the early solar system, and the isotopic compositions of volatiles accreted by the terrestrial planets.
The poorly characterized phase (PCP) of the Mighei CM2 carbonaceous chondrite is investigated using high-resolution TEM. Electron-microprobe analyses of samples from both olivine chondrules and the matrix are included in a table. Chondrule PCP is found to have higher concentrations of S and Ni and lower concentrations of Si, Mg, and Al than matrix PCP. TEM shows that PCP in this chondrite is an intergrowth of three phases (in various proportions): a major component containing Fe, S, Ni, and O in wavy rolled layers spaced about 5.4 A apart, an Fe-rich serpentinelike phyllosilicate with 7-A layer spacing, and submicron grains of magnetite, chromite, and phosphate. It is proposed that chondrule PCP contains mainly the 5-A phase with some grains, while matrix PCP consists mostly of the 5-A and 7-A phases.
The morphology and inclusions of individual Mg rich olivine grains from C2 chondrites provide disputed evidence for origin either from a liquid or a vapor. Olivine grains from Murchison (C2) and Allende (C3) meteorites were examined to extend data on Belgica 7904 (C2. Cathodoluminescence revealed the relation of chemical zoning to external shape and inclusions. High precision electron probe analyses of selected spots for Na, Al, P, Ca, Ti, Cr and Mn provided chemical constraints on the source material. From several possible explanations tentative suggestions are for at least two stages: (1) growth of the blue core from a vapor enriched in refractory elements (hence lack of inclusions); and (2) growth of red/dark rim from an unenriched liquid which entrapped the blue core. Mechanical transfer may be involved. The channels and networks are puzzling at this time. Whatever the true explanation, a complex history is needed for a simple mineral, and further study should provide additional restraints on formation of carbonaceous meteorites.
Cathodoluminescence has been applied to look for textural features of olivine in carbonaceous meteorites relevant to the unresolved dispute over the origin of the olivine, whether from a vapor or a liquid. Cathodoluminescence photographs of forsterite grains in Murchison (C2) and Allende (C3) meteorites presented here reveal a blue core with planar boundaries to a red or dark rim. High-precision electron microprobe analyses have been performed which reveal unusually large amounts of the 'minor' elements Al, Ti, and Ca in the blue cores of these forsterites, suggesting formation by crystallization at high temperatures from a source rich in these metals. Following conclusions drawn from previous analyses of olivine in meteorites, it is argued that the minor element signature should be able to characterize olivines in micrometeorites and in deep-sea particles.
The technique developed by Kornacki (1984) for identifying group II Ca/Al-rich inclusions in carbonaceous chondrites by electron-microprobe analysis of the ZrO2 or Y2O3 content of their perovskite component is demonstrated using material from 20 Allende inclusions. The results are presented in tables and graphs and compared with findings obtained by other procedures. Group II inclusions are found to have perovskites generally containing less than 0.10 wt pct ZrO2 and/or Y2O3 (average of several grains), while those of groups I, III, V, and VI have more than 0.25 wt pct ZrO2. Analysis of data on eight Allende Ca/Al-rich inclusions shows that 75 percent of the fine-grained inclusions belong to group II. The implications of these findings for fractionation processes in the primitive solar nebula are indicated.
Xe isotopic measurements are described. The samples analyzed were bulk chips of the Murray (C2) and Murchison (C2) carbonaceous chondrites that had been freeze-thaw disaggregated, etched with H2O2, and then split into colloidal and noncolloidal fractions using methanol. The etching removed a substantial portion of the trapped Xe and increased variations in measured isotopic ratios compared with bulk sample analyses. The Murray samples appeared to contain a binary mixture of U-Xe and H+L-Xe. The Murchison data concur with the Murray data for the heavy isotopes, but the structure at the light isotopes is obscured by spallation Xe. There is no evidence in these data for the separability of H-Xe and L-Xe. The fact that H2O2 etching removes Xe without prior demineralization supports the view that the carrier of a substantial portion of trapped Xe may reside on grain surfaces.
The carbonaceous meteorites were studied. The studies which were conducted have evolved from investigations of early irradiation to mineralogic and petrologic studies of refractory inclusions and to an examination of the time scales of alteration processes on the parent bodies. The attached listing of papers and abstracts provide the details.