Origin of the hydrocarbon component of carbonaceous chondrites: the star-meteorite connection

We report the results of an experiment that produced a residue which closely matches the hydrocarbon component of the Murchison carbonaceous chondrite. This experiment suggests that the parent material of the meteoritic component originated as polycyclic aromatic hydrocarbon species in carbon stars during their later stages of evolution. The experiments also indicate that the pathway from those formation sites to eventual incorporation into the meteorite parent body involved hydrogenation in a plasma in the solar nebula or in H II regions prior to the solar nebula. This model is consistent with what is known about the meteoritic hydrocarbon component including deuterium abundance, the observation of cosmic infrared emission bands best attributed to polycyclic aromatic hydrocarbon molecules, and the inherent stability of these molecules that allows their formation in stars and subsequent survival in the interstellar medium.     

Microwave emission from a sunspot

From the gyroresonance brightness temperature spectrum of a sunspot, one can determine the magnetic field strength by using the property that microwave brightness is limited above a frequency given by an integer-multiple of the gyrofrequency. In this paper, we use this idea to find the radial distribution of magnetic field at the coronal base of a sunspot in the active region, NOAA 4741. The gyroresonance brightness temperature spectra of this sunspot are obtained from multi-frequency interferometric observations made at the Owens Valley Radio Observatory at 24 frequencies in the range of 4.0–12.4 GHz with spatial resolution 2.2″–6.8″. The main results of present study are summarized as follows: first, by comparison of the coronal magnetic flux deduced from our microwave observation with the photospheric magnetic flux measured by KPNO magnetograms, we show that theo-mode emission must arise predominantly from the second harmonic of the gyrofrequency, while thex-mode arises from the third harmonic. Second, the radial distribution of magnetic fieldsB(r) at the coronal base of this spot (say, 2000–4000 km above the photosphere) can be adequately fitted by $$B(r) = 1420(1 \pm 0.080)\exp \left[ { - \left( {\frac{r}{{11.05''(1 \pm 0.014)}}} \right)^2 } \right]G,$$ wherer is the radial distance from the spot center at coronal base. Third, it is found that coronal magnetic fields originate mostly from the photospheric umbral region. Fourth, although the derived vertical variation of magnetic fields can be approximated roughly by a dipole model with dipole moment 1.6 × 10³⁰ erg G^?1 buried at 11000 km below the photosphere, the radial field distribution at coronal heights is found to be more confined than predicted by the dipole model.     

Geochronology and geochemistry of eclogites from the Mariánské Lázně Complex,Czech Republic: Implications for Variscan orogenesis

The Mariánské Lázn complex (MLC) is located in the Bohemian Massif along the north-western margin of the Teplá-Barrandian microplate and consists of metagabbro, amphibolite and eclogite, with subordinate amounts of serpentinite, felsic gneiss and calcsilicate rocks. The MLC is interpreted as a metaophiolite complex that marks the suture zone between the Saxothuringian rocks to the north-west and the Teplá-Barrandian microplate to the south-east. Sm-Nd geochronology of garnet-omphacite pairs from two eclogite samples yields ages of 377±7, and 367±4 Ma. Samples of eclogite and amphibolite do not define a whole rock Sm-Nd isochron, even though there is a large range in Sm/Nd ratio, implying that the suite of samples may not be cogenetic. Eclogites do not have correlated _Nd values and initial ⁸⁷Sr/⁸⁶Sr ratios. Five of the eight eclogite samples have high _Nd values (+10.2 to +7.1) consistent with derivation from a MORB-like source, but variable ⁸⁷Sr/⁸⁶Sr ratios (0.7033 to 0.7059) which probably reflect hydrothermal seawater alteration. Three other eclogite samples have lower _Nd values (+ 5.4 to –0.8) and widely variable ⁸⁷Sr/⁸⁶Sr ratios (0.7033 to 0.7096). Such low _Nd values are inconsistent with derivation from a MORB, source and may reflect a subduction or oceanic island basalt component in their source. The MLC is an important petrotectonic element in the Bohemian Massif, providing evidence for Cambro-Ordovician formation of oceanic crust and interaction with seawater, Late Devonian (Frasnian-Famennian) high- and medium-pressure metamorphism related to closure of a Saxothuringian ocean basin, Early Carboniferous (Viséan) thrusting of the Teplá terrane over Saxothuringian rocks and Late Viséan extension.     

Plasma processing of interstellar PAHs into solar system kerogen

Processes resulting in the formation of hydrocarbons of carbonaceous chondrites and the identity of the interstellar molecular precursors involved are an objective of investigations into the origin of the solar system and perhaps even life on earth. We have combined the resources and experience of an astronomer and physicists doing laboratory simulations with those of a chemical expert in the analysis of meteoritic hydrocarbons, in a project that investigated the conversion of polycyclic aromatic hydrocarbons (PAHs) formed in stellar atmospheres into alkanes found in meteorites. Plasma hydrogenation has been found in the University of Alabama at Birmingham Astrophysics Laboratory to produce from the precursor PAH naphthalene, a new material having an IR absorption spectrum (Lee, W. and Wdowiak, T.J., Astrophys. J. 417, L49-L51, 1993) remarkably similar to that obtained at Arizona State University of the benzene-methanol extract of the Murchison meteorite (Cronin, J.R. and Pizzarello, S., Geochim. Cosmochim. Acta 54, 2859-2868, 1990). There are astrophysical and meteoritic arguments for PAH species from extra-solar sources being incorporated into the solar nebula, where plasma hydrogenation is highly plausible. Conversion of PAHs into alkanes could also have occurred in the interstellar medium. The synthesis of laboratory analogs of meteoritic hydrocarbons through plasma hydrogenation of PAH species is underway, as is chemical analysis of those analogs. The objective is to clarify this heretofore uninvestigated process and to understand its role during the origin of the solar system as a mechanism of production of hydrocarbon species now found in meteorites. Results have been obtained in the form of time-of-flight spectroscopy and chemical analysis of the lab analog prepared from naphthalene.     

On the astrometric detection of neighboring planetary systems,II

Extensive testing suggests that astrometric techniques can be employed to detect and study virtually any planetary system that may exist within 40 light years (12.5 parsec) of the Sun. Following the conclusion of Paper I [G. Gatewood, Icarus27 (1976), 1–12], the astrometric group at the Allegheny Observatory began an intensive survey of 20 nearby stars to detect the nonlinear variations in their motion that planetary systems would induce. Several tests conducted to further our understanding of the limitations of this survey indicated that the photographic detector itself is responsible for the majority of the random error. A new photoelectric detector has been designed and a simplified prototype of it successfully tested. The new detector is expected to be able to utilize virtually all of the astrometric information transmitted through the Earth's atmosphere. This is sufficient to determine relative positions to within an accuracy of approximately 1 milliarcsec/hr. Such precisions exceed the design capabilities of the best existing astrometric telescopes, thus a feasibility study has been conducted for the design of an improved instrument. The study concludes that a new ground-based telescope and the new detector combined should be able to study stars as faint as the 17th magnitude with an annual accuracy of a few tenths of a milliarcsecond. However, to obtain the ultimate accuracy possible from current technology, we must place an astrometric system above the Earth's atmosphere. A space-borne instrument utilizing the new detector would in theory have sufficient accuracy to detect any Earth-like planet orbiting any of the several hundred stars nearest the Sun.     

Coherent amplification and pulsar phenomena

A modification of the rotating-star model has been developed to interpret the periodic energy bursts from pulsars. This new configuration involves -directed oscilltion modes in the stellar atmosphere or magnetosphere, and most aspects of the typical pulse characteristics are well accounted for. Gain is provided by resonant interactions with particles trapped in the stellar magnetic field. The most significant feature is the fact that highly directional beaming of the output energy results as a natural consequence of coherence between the radiation fields emerging from various locations about the pulsar; and a localized radiation origin is not required.     

M computed from strong motion accelerograms recorded in Yugoslavia

It is shown that the new definition¹ of strong motion local magnitude M leads to stable estimates of magnitudes for earthquakes in Yugoslavia, with epicentral distances R <100 km and for 2.5 < M < 6.5. Tables with magnitudes computed using this new procedure are presented for all earthquakes contributing to the strong motion accelerogram files in EQINFOS for Yugoslavia.² The similarity of our findings with the analogous analyses for California suggests new possibilities for relative calibration between various local magnitude scales, which are used in southeastern Europe, and M_L in California.     

Drying effects on sorption capacity of coastal sediment: The importance of architecture and polarity of organic matter

Investigations on how desiccation changes sorption of organic compounds by salt marsh sediments provide insight into the physical and chemical properties of these wide-spread coastal sediments. We measured sorption of compounds with different polarities (lysine, tyrosine, naphthalene and aniline) onto natural sediments and sediments that were dried and rewetted. Sorption of lysine by marsh sediment decreased significantly when the sediment was dried using a freeze-drier, oven, or desiccator, and sorption capacity was not restored when sediments were rewetted. In contrast to lysine, the sorption capacity of more hydrophobic compounds (tyrosine, aniline and naphthalene) increased significantly after salt marsh sediment was dried. These results suggest that drying greatly increased sediment hydrophobicity. Consistently, water drop penetration time, an index of hydrophobicity, was significantly lower for combusted sediments than for those that were simply dried. Sediments treated with EDTA, or boiled in seawater, exhibited a similar or even greater reduction in lysine sorption capacity compared with sediments that were dried. Water retention capacity of salt marsh sediment decreased 50% after sediment was dried. The effects of pH and salinity on lysine sorption in wet and dry sediments suggest that carboxyl groups play a major role in lysine sorption through cation ion exchange, and drying may reduce access to carboxyl groups. We hypothesize that the three-dimensional (3D) structure of organic matter, originating mainly from Spartina alterniflora, is an important factor controlling sorption capacity in salt marsh sediment. The drying process makes sedimentary organic matter change conformation, shrink in volume, and expose hydrophobic groups, thus becoming more hydrophobic. In environments with wet and dry cycles, the distribution of hydrophobic or hydrophilic compounds between solution and particulate phases could thus be influenced by the 3D structure and polarity of organic matter.     

Oil-generation kinetics for organic facies with Type-II and -IIS kerogen in the Menilite Shales of the Polish Carpathians

The Menilite Shales (Oligocene) of the Polish Carpathians are the source of low-sulfur oils in the thrust belt and some high-sulfur oils in the Carpathian Foredeep. These oil occurrences indicate that the high-sulfur oils in the Foredeep were generated and expelled before major thrusting and the low-sulfur oils in the thrust belt were generated and expelled during or after major thrusting. Two distinct organic facies have been observed in the Menilite Shales. One organic facies has a high clastic sediment input and contains Type-II kerogen. The other organic facies has a lower clastic sediment input and contains Type-IIS kerogen. Representative samples of both organic facies were used to determine kinetic parameters for immiscible oil generation by isothermal hydrous pyrolysis and S₂ generation by non-isothermal open-system pyrolysis. The derived kinetic parameters showed that timing of S₂ generation was not as different between the Type-IIS and -II kerogen based on open-system pyrolysis as compared with immiscible oil generation based on hydrous pyrolysis. Applying these kinetic parameters to a burial history in the Skole unit showed that some expelled oil would have been generated from the organic facies with Type-IIS kerogen before major thrusting with the hydrous-pyrolysis kinetic parameters but not with the open-system pyrolysis kinetic parameters. The inability of open-system pyrolysis to determine earlier petroleum generation from Type-IIS kerogen is attributed to the large polar-rich bitumen component in S₂ generation, rapid loss of sulfur free-radical initiators in the open system, and diminished radical selectivity and rate constant differences at higher temperatures. Hydrous-pyrolysis kinetic parameters are determined in the presence of water at lower temperatures in a closed system, which allows differentiation of bitumen and oil generation, interaction of free-radical initiators, greater radical selectivity, and more distinguishable rate constants as would occur during natural maturation. Kinetic parameters derived from hydrous pyrolysis show good correlations with one another (compensation effect) and kerogen organic-sulfur contents. These correlations allow for indirect determination of hydrous-pyrolysis kinetic parameters on the basis of the organic-sulfur mole fraction of an immature Type-II or -IIS kerogen.     

Source(s) and cycling of the nonhydrolyzable organic fraction of oceanic particles

A major fraction of particulate organic carbon (POC) in the deep ocean remains molecularly uncharacterized. In an effort to determine the chemical characteristics and source(s) of sinking POC, we studied a nonhydrolyzable fraction of sinking POC using ¹³C NMR (nuclear magnetic resonance) spectroscopy and analytical pyrolysis. ¹³C NMR spectra and products from analytical pyrolysis of the nonhydrolyzable fraction exhibit a strongly aliphatic character that is distinct from that of bulk POC. The aliphatic nature of this fraction is consistent with its low stable carbon isotope values. We hypothesize that the nonhydrolyzable fraction derives to a significant extent from a refractory component of organisms that selectively accumulates, resulting in its manifestation as a major part of POC sinking to the deep ocean and in underlying sediments.