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Anders, E.

Publications and source records attributed to Anders, E..

At least 37 records · Page 2
All sourcesNASA NTRSDOE OSTI
NASA NTRS1982

Solar-system abundances of the elements

Elemental analyses of the Ogueil Cl meteorite and all previous Cl chondrite analyses were employed to develop a new solar system abundance table, including the standard deviation and number of analyses for each element. The table also comprises the abundances of radioactive and radiogenic nuclides at the present and 4.55 AE ago, as well as abundances by weight in a typical Cl chondrite. The new abundances were within 20% of those determined by Cameron (1982), except for 14 cases in the range 20-50%, and 5 over 50%. The solar abundances were compared with the Cl abundances, showing a total of only 7 disagreements. No significant discrepancies were detected in the major cosmochemical groups, and a smooth trend was found in the abundances of odd-A nuclides. The new set is interpreted as accurate to 10%, with the Cl chondrites matching the primordial solar system abundances to at most 10% deviation.

Anders, E.↗
NASA NTRS1982

Are C1 chondrites chemically fractionated - A trace element study

Six C1 chondrite samples and a C2 xenolith from the Plainview H5 chondrite were analyzed by radiochemical neutron activation for a large variety of elements, including rare earths. The sample processing is described, including the irradiation, chemical procedure, rare earths separation, counting techniques, radiochemical purity check, and chemical yields. The results of consistency checks on a number of elements are discussed. Abundances for siderophiles, volatiles, and rare earths are presented and discussed. Tests are presented for fractionation of rare earths and other refractories, compositional uniformity of C1's, and interelement correlations. There is no conclusive evidence for nebular fractionation affecting C1's. Three fractionation-prone rare earths have essentially the same relative abundances in C1's and all other chondrite classes, and hence are apparently not fractionated in C1's.

Ebihara, M.↗
NASA NTRS1982

Sorption of noble gases by solids, with reference to meteorites. I - Magnetite and carbon

The trapping of meteoritic noble gases by solids is simulated through the synthesis of 18 Fe3O4 samples at 350-720 K in a noble gas atmosphere, by means of the reactions: (1) 3Fe + 4H2O yields Fe3O4 + 4H2, using Ne, Ar, Kr and Xe; and (2) 3Fe + 4CO yields Fe3O4 + 4C + carbides, using Xe. Etching experiments suggest an analogy with 'Phase Q' in meteorites. Adsorbed atmospheric gases are present in all samples, and dominate whenever the noble gas partial pressure in the atmosphere is greater than that in the synthesis. While many of the results of Lancet and Anders (1973) appear to have been dominated by such an atmospheric component, others are suspect. When the doubtful samples of Lancet and Anders are corrected or eliminated, the fractionation pattern no longer peaks at Ar, but rather, as in the present sample, rises monotonically from Ne to Xe. No evidence is found for the earlier study's claim of a strong temperature dependence.

Yang, J.↗
NASA NTRS1982

Sorption of noble gases by solids, with reference to meteorites. II - Chromite and carbon. III - Sulfides, spinels, and other substances; on the origin of planetary gases

The trapping of noble gases by chromite and carbon, two putative carriers of primordial noble gases in meteorites, was studied by synthesizing 19 samples in a Ne-Ar-Kr-Xe atmosphere at 440-720 K. Noble gas contents are found to approximately obey Henry's Law, but only slight correlations are found with composition, surface area, or adsorption temperature. Geometric mean distribution coefficients for bulk samples and HCl residues in 10 cu cm STP/g atm are: Xe 100, Kr 15, Ar 3.5, and Ne 0.62. Elemental fractionation data support the suggestion of Lewis et al. (1977) that chromite and carbon in C2 and C3 chondrites were formed by the reaction: Fe, Cr + 4CO yields (Fe, Cr)3O4 + 4C + carbides. In contrast to meteoritic minerals, the synthetic specimens show no isotopic fractionation of noble gases. In a subsequent study, attention is given to the cases of sulfides and spinels, on the way to consideration of the origin of planetary gases. Sulfides showed three distinctive trends relative to chromite or magnetite. The elemental fractionation pattern of Ar, Kr and Xe in meteorites, terrestrial rocks and planets resembles the adsorption patterns on the carbons, spinels, sulfides, and other solids studied. The high release temperature of meteoritic noble gases may be explained by transformation of the physisorbed or chemisorbed gas. The ready loss of meteoritic heavy gases on surficial oxidation is consistent with adsorption, as is the high abundance.

Yang, J.↗
NASA NTRS1981

Noble gases in E-chondrites

The combination of noble gas data for 12 E-chondrites with literature data shows K-Ar ages greater than 4 AE for 14 out of 18 meteorites, while U, Th-He ages are often shorter. Cosmic ray exposure ages are found to differ systematically between types E4 and E6, with the respective, below-16 Myr and above-30 Myr values implying that the E-chondrite parent body predominantly contains a single petrologic type on the 1 km scale of individual impacts in contrast to the mixed parent bodies of the ordinary chondrites. Amounts of planetary gas in E4-E6 chondrites fall in the range for ordinary chondrites of types 4-6, but fail to correlate with petrologic type or volatile trace element contents, in contrast to the ordinary chondrites. Analyses of mineral separates show that the planetary gases are concentrated in an HFand HCl-insoluble mineral, similar to phase Q. The subsolar gases are located in an HCl- and HNO3-resistant phase.

Crabb, J.↗
NASA NTRS1981

Isotopically anomalous xenon in meteorites - A new clue to its origin

The CCF xenon component in primitive meteorites, which has been attributed either to fission of a superheavy element or to nucleosynthesis in a supernova, does not show the large enrichment in Xe-129 (from decay of 16 Myr I-129) expected for supernova ejecta. Although this problem can be circumvented by ad hoc assumptions, a fission origin of CCFXe seems more likely.

Lewis, R. S.↗
NASA NTRS1981

Organic compounds in meteorites and their origins

The current investigation represents an extensively updated version of a review conducted by Anders et al. (1973). The investigation takes into account the literature through mid-1980. It is pointed out that Type 1 carbonaceous chondrites (C1) contain 6% of their cosmic complement of carbon, mainly in the form of organic matter. Most authors now agree that this material represents primitive prebiotic matter. The principal questions remaining are what abiotic processes formed the organic matter, and to what extent these processes took place in locales other than the solar nebula, such as interstellar clouds or meteorite parent bodes. The problem is approached in three stages. It is attempted to reconstruct the physical conditions during condensation from the clues contained in the inorganic matrix of the meteorite. The condensation behavior of carbon under these conditions is determined on the basis of thermodynamic calculations. Model experiments on the condensation of carbon are performed, and the synthesized compounds are compared with those actually found in meteorites.

Hayatsu, R.↗
NASA NTRS1980

Moon and earth - Compositional differences inferred from siderophiles, volatiles, and alkalis in basalts

A comparison of RNAA analyses of 18 trace elements in 25 low-Ti lunar and 10 terrestrial oceanic basalts indicated that the volatiles such as Ag, Bi, and Br are depleted in lunar basalts by nearly constant factors of 0.026 relative to terrestrial basalts. This constancy is not consistent with models that derive the moon's volatiles from partial recondensation of the earth's mantle or from partial degassing of a captured body; it is consistent with models which derive planetary volatiles from a thin veneer of C-chondrite material. Chalcogens (Se and Te) have almost constant and identical abundances in lunar and terrestrial basalts; siderophiles show abundant Ni in lunar basalts, while Ir, Re, Ge, and Au are depleted.

Wolf, R.↗
NASA NTRS1980

Chemical composition of earth, Venus, and Mercury

Model compositions of the earth, Venus, and Mercury are calculated from the premise that planets and chondrites underwent four identical fractionation processes in the solar nebula. Because elements of similar properties stay together in these processes, five constraints suffice to define the composition of a planet: mass of the core, abundance of U, and the ratios K/U, TI/U, and FeO/(FeO + MgO). Complete abundance tables, and normative mineralogies, are given for all three planets. A review of available data shows only a few gross trends for the inner planets: FeO decreases with heliocentric distance, whereas volatiles are depleted and refractories are enriched in the smaller planets.

Morgan, J. W.↗
NASA NTRS1980

Carbynes - Carriers of primordial noble gases in meteorites

Five carbynes (triply bonded allotropes of carbon) have been found by electron diffraction in the Allende and Murchison carbonaceous chondrites: carbon VI, VIII, X, XI, and (tentatively) XII. From the isotopic composition of the associated noble-gas components, it appears that the carbynes in Allende (C3V chondrite) are local condensates from the solar nebula, whereas at least two carbynes in Murchison (C2 chondrite) are of exotic, presolar origin. They may be dust grains that condensed in stellar envelopes and trapped isotropically anomalous matter from stellar nucleosynthesis.

Whittaker, A. G.↗
NASA NTRS1980

Carbynes in meteorites - Detection, low-temperature origin, and implications for interstellar molecules

The presence, origin and implications of carbynes in meteorites are investigated. A sample of the Allende meteorite was pyrolyzed at temperatures from 25 to 750 C and examined by solid probe time-of-flight mass spectrometry and high-resolution mass spectrometry. Fragments released upon heating at 250 to 330 C are found to be composed of macromolecules containing triply bonded carbon units and cyanoacetylenes, as well as some methyl- and phenylacetylenes. Although carbynes are well known to form from the condensation of carbon vapors above 2600 K or by shock greater than 600 kbar, which would be unlikely in Allende, it is found that carbynes rather than graphite are formed metastably by the disproportionation of CO at low temperatures when chromite is present as a catalyst. Results imply that metastable formation mechanisms may be the principal source of interstellar polycyanoacetylenes and meteoritic and terrestrial carbynes.

Hayatsu, R.↗
NASA NTRS1980

Chemical fractionations in meteorites. XI - C2 chondrites

Measurements of the compositions of 20 trace elements in the representative C2 chondrites Boriskino, Cold Bokkeveld, Erakot, Essebi, Haripura, Santa Cruz and Al Rais are reported. The contents of Ag, Au, Bi, Cd, Cs, Ge, In, Ir, Ni, Os, Pd, Rb, Re, Sb, Se, Sn, Te, Tl, U, and Zn were determined by radiochemical neutron activation analysis. The siderophile abundances of the C2 chondrites are found to be less uniform than those of other carbonaceous chondrites, while the C2R chondrite Al Rais is systematically lower in 12 volatiles than the C2M chondrites. Enrichment of Bi and Tl found in Erakot and Haripura indicate the possible presence of the late condensate mysterite. Volatile abundances are shown to agree with matrix contents for meteorites that have suffered little aqueous alteration, however to be 20-30% lower for the more altered meteorites. Finally, the decline of element abundance with volatility is shown to be consistent with the sigmoid curve explained by the two-component model.

Wolf, R.↗
NASA NTRS1980

Neutron capture time scale of the s-process, estimated from s-process krypton in a meteorite

A krypton fraction enriched in s-process isotopes was extracted from a mineral fraction of the Murchison C2 chondrite. The (Kr-86)/(Kr-84) ratio is enhanced by 6 standard deviations, showing that significant amounts of Kr-86 were made in the s-process, despite the short, 10.8 yr beta-decay half-life of its precursor, Kr-85. Judging from this sample, the mean neutron capture time in the s-process was on the order of 5-100 yr for nuclei with cross sections of 125 mb.

Matsuda, J.-I.↗
NASA NTRS1980

Isotopic anomalies of noble gases in meteorites and their origins. VI Presolar components in the Murchison C2 chondrite

Rare gases were analyzed by stepped heating in five fractions of a chemically resistant residue from Murchison that had been separated according to grain size and resistance to HClO4. Nine gas components were recognized, of which three appear to be presolar: (1) Ne-E(H) released at 1000-1600 C and located in spinel; (2) Ne-E(L) released at less than 800 C and apparently located in a carbonaceous phase of grain size up to 10 microns; and (3) s-process Xe and Kr released at 1200-1600 C and located in a poorly characterized, possibly carbonaceous phase, distinct from the host phase of Ne-E(L).

Alaerts, L.↗
NASA NTRS1979

Stellar condensates in meteorites - Isotopic evidence from noble gases

The Murchison carbonaceous chondrite contains three isotopically anomalous noble-gas components of apparently presolar origin: two kinds of Ne-E, (Ne-20)/(Ne-22) less than 0.6, and s-process Kr + Xe (enriched in the even isotopes 82, 84, 86, 128, 130, 132). Their carriers are tentatively identified as spinel and two carbonaceous phases, the principal high-temperature stellar condensates at low and high C/O ratios, respectively.

Lewis, R. S.↗