Kinetic envelope solitons in turbulent plasmas

A non-linear Schrödinger equation which characterizes the non-linear electrostatic waves in collisionless turbulent plasma is derived. Detailed analysis of this equation for the non-linear Langmuir waves is presented to show how the ion dynamics affects the envelope behaviour of these waves. Necessary condition for the existence of Langmuir envelope solitons is found to bek ² _D ² (m/M);k being the characteristic wave number, _D the electron Debye length andm andM the electron and the proton mass.Paper dedicated to Professor Hannes Alfvén on the occasion of his 70th birthday, 30 May, 1978.     

A new model for X-ray emission from NGC 4151

We present an analysis of the reported spectral features of NGC 4151 in X-rays. It is shown that the origin of X-rays from the source is inconsistent with a single production mechanism. We suggest a new two-component model in which soft X-rays arise from the black-body emission of a tiny hot nucleus withT2×10⁷ K and the hard X-ray photons are generated in an extended region by inverse Compton scattering of electrons with the infrared photons.     

Noble gases in the Allende and Abee meteorites and a gas-rich mineral fraction: investigation by stepwise heating

Noble gases in three meteoritic samples were examined by stepwise heating, in an attempt to relate peaks in the outgassing curves to specific minerals: NeKrXe in Allende (C3V) and an Allende residue insoluble in HF-HCl, and Xe in Abee (E4). In Allende, chromite and carbon contain most of the trapped Ne (²⁰Ne/²²Ne ≈ 8.7) and anomalous Xe enriched in light and heavy isotopes, and release it at ~850°C (bulk meteorite) or 1000°C (residue). Mineral Q, containing most of the trapped Ar, Kr, Xe as well as some Ne (²⁰Ne/²²Ne ≈ 10.4), releases its gases mainly between 1200 and 1600°C, well above the release temperatures of organic polymers (300–500°) or amorphous carbon (800–1000°). The high noble-gas release temperature, ready solubility in oxidizing acids, and correlation with acid-soluble Fe and Cr all point to an inorganic rather than carbonaceous nature of Q.All the radiogenic ¹²⁹Xe is contained in HCl, HF-soluble minerals, and is distributed as follows over the peaks in the release curve: Attend 1000° (75%), 1300° (25%); Abee (data of Hohenberg and Reynolds, 1969) ~850° (15%), 1100° (60%), 1300° (25%). No conclusive identifications of host phases can yet be given; possible candidates are troilite and silicates for Allende, and djerfisherite, troilite and silicates for Abee.Mineral Q strongly absorbs air xenon, and releases some of it only at 800–1000°C. Dilution by air Xe from Q and other minerals may explain why temperature fractions from bulk meteorites often contain less ^124–130Xe for a given enrichment in heavy isotopes than does xenon from etched chromitecarbon samples, although chromite-carbon is the source of the anomalous xenon in either case. Air xenon contamination thus is an important source of error in the derivation of fission xenon spectra.     

Comparison of crude oils and their alteration products

A simple method is proposed for using gas Chromatographic data on the high molecular weight saturated fractions of crude oils to make comparisons of source materials, migration mechanisms and, in particular, alteration processes within reservoirs. The preferential loss of normal alkanes by bacterial attack on a light crude is one of several processes readily followed using this scheme.     

Formation of the Bencubbin polymict meteoritic breccia

The Bencubbin meteorite is a polymict breccia consisting of a host fraction of ~60% metal and ~40% ferromagnesian silicates and a selection of carbonaceous, ordinary and ‘enstatite’ chondritic clasts. Concentrations of 27 elements were determined by neutron activation in replicate samples of the host silicates and the ordinary and carbonaceous chondritic clasts; 12 elements were determined in the host metal. Compositional data for the ordinary chondrite clast indicate a classification of LL4 ± 1. Refractory element data for the carbonaceous chondrite clast indicate that it belongs to the CI-CM-CO clan; its volatile element abundances are intermediate between those of CM and CO chondrites. Abundances of nonvolatile elements in the silicate host are similar to those in the carbonaceous chondrite clast and in CM chondrites; the rare earths are unfractionated. We conclude that it is not achondritic as previously designated, but chondritic and that it is probably related to the CI-CM-CO clan; its volatile abundances are lower than those in CO chondrites. Oxygen isotope data are consistent with these classifications. Host metal in Bencubbin and in the closely related Weatherford meteorite has low abundances of moderately volatile siderophiles; among iron meteorite groups its nearest relative is group IIIF.We suggest that Bencubbin and Weatherford formed as a result of an impact event on a carbonaceous chondrite regolith. The impact generated an ‘instant magma’ that trapped and surrounded regolithic clasts to form the polymict breccia. The parent of this ‘magma’ was probably the regolith itself, perhaps mainly consisting of the so-called ‘enstatite’ chondrite materials. Accretion of such a variety of materials to a small parent body was probably only possible in the asteroid belt.     

The chemistry of orthophosphate uptake from seawater on to calcite and aragonite

The chemistry of orthophosphate uptake from synthetic seawater onto the surfaces of synthetic calcite, aragonite and low-magnesium biogenic calcite has been studied, in order to elucidate the kinetics of the process (generally believed to be the major control of dissolved reactive phosphate in carbonate-rich marine sediments). Our results differ from those obtained by others, who have studied orthophosphate uptake in low ionic strength solutions and at much higher supersaturations relative to apatite.In both ‘free drift’ and chemostat experiments, Mg and F have only a minor effect on the reaction rate. Even at constant solution composition the rate of orthophosphate uptake was found to decrease by 10⁶ over a two week period. The data from the ‘free drift’ experiments can be fitted to the Elovich equation. This indicates that the kinetics observed for this reaction can be explained by an exponential decrease in available surface reaction sites and/or a linear increase in the activation energy associated with chemisorption as the reaction proceeds.     

The formation and clay mineral reactions of melanoidins

Sugars and amino acids condense readily to form polymers known as melanoidins that closely resemble natural humic substances. In this study melanoidins are formed by reacting glucose with each of three amino acids: glutamic acid, valine and lysine. The basic amino acid, lysine, reacts with glucose at a much greater rate than either of the other two compounds. The chemical properties of the melanoidins are strongly influenced by the amino acid from which they are formed. The nitrogen contents, acidities and electrophoretic behavior of the polymers all reflect functional group distributions inherited from the amino acids. These chemical differences strongly influence the extent of association of the melanoidins with kaolinite and montmorillonite clay minerals. Laboratory simulations suggest that melanoidin formation may be favored in marine environments where basic amino acids should preferentially condense with sugars to form nitrogen-rich polymers that have a great affinity for clay mineral surfaces.