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At least 91 records · Page 5

The relation between the chemical composition of solar cosmic rays and the duration spectrum of radiosplashes

The comparison of durations of the centimeter and meter components of the radiosplashes corresponding to the chromospheric flares with the known chemical composition of the radiated nuclei has shown a greater duration of the centimeter component for the splashes wherein protons are dominating, and vice versa. A conclusion is made about the interrelation of heavy nucleus emission and the processes which occur in the upper layers of the solar corona.

Tsimakhovich, N. P.↗

RR Lyrae stars and the distant Galactic halo - Distribution, chemical composition, kinematics, and dynamics

Published observational data on 29 outer-Galactic-halo RR Lyr stars (Saha, 1984, and Saha and Oke, 1984) and from other surveys are analyzed to characterize the mass distribution, chemical composition, kinematics, and dynamics of the outer Galaxy (up to galactocentric radius R = 40 kpc). The results are presented in graphs and tables and discussed. Findings reported include a rapid fall-off of RR Lyr density at R = 25 kpc, Fe/H varying from -1.0 to -2.2 (with two stars at -0.5), no net Fe/H gradient in the far halo, and Galactic mass (from dynamical computations) about 3 x 10 to the 11th solar mass within R = 25 kpc.

Saha, A.↗

Chemical composition of boulder-2 rocks and soils, Apollo 17, Station 2

The bulk and trace element composition of five small samples from four rocks is remarkably similar. This result indicates that the metaclastic rocks studied are relatively uniform in their chemical composition. The elemental abundances found in the study are presented in two tables and the implications of the data are considered, giving attention to siderophiles, atmophile elements, and questions of element correlations. The 'dark mantle' valley soil 75081 at Camelot Crater is low in siderophiles. Since the soil is low in alkalis, a derivation from low-alkali mare basalt is suggested. The identical volatile contents in the surface soil 72461 and the 4 cm depth soil 72441 under a 0.7 m boulder argue against any surficial volatization by galactic and solar particles.

Laul, J. C.↗

Ultraviolet spectrum and probable chemical composition of the high-excitation planetary nebula M1-1

Data obtained with the IUE and with the image-tube scanner on the Shane 3-m telescope at the Lick Observatory were used to determine the possible chemical composition of the high excitation nebula, M1-1. Though N may be enhanced, the composition of M1-1 does not seem to differ significantly from that of the sun, in contrast to NGC 6537. M1-1 abundances do not appear to differ by more than about a factor of two from those of the mean planetaries or the sun. NGC 6537 and NGC 6302 show large effects of nuclear processing in C, N, and possibly O, while M1-1, in spite of its high excitation and presumed origin from a relatively massive star, shows insignificant effects of nuclear processing.

Aller, L. H.↗

Study of mass flow distribution and chemical composition of comets from solar induced X-ray fluorescence

The expected performance of an X-ray detector as an instrument aboard a mission to a comet was evaluated. The functions of the detector are both nondispersive analysis of chemical composition and measurement of mass flow from the comet nucleus. Measurements are to be carried out at a distance from the comet. The approach distances considered are of the order of 1000 km and 100 km. A new type of X-ray detector, a proportional scintillation detector, is considered as an X-ray counter for nondispersive elemental analysis.

Gorenstein, P.↗

Extraterrestrial spherules in glacial sediment from the Transantarctic Mountains, Antarctica - Structure, mineralogy, and chemical composition

The morphological, mineralogical, and chemical characteristics of silicate and glassy spherules from a number of new localities in the Transantarctic Mountains were determined. The results indicate that these Antarctic spherules are of extraterrestrial origin. It is concluded that they, most likely, represent individual micrometeorites that melted during passage through the atmosphere; alternatively, they may be ablation spherules.

Koeberl, Christian↗

Aerosol Optical Properties Measured Onboard the Ronald H. Brown During ACE Asia as a Function of Aerosol Chemical Composition and Source Region

During the ACE Asia intensive field campaign conducted in the spring of 2001 aerosol properties were measured onboard the R/V Ronald H. Brown to study the effects of the Asian aerosol on atmospheric chemistry and climate in downwind regions. Aerosol properties measured in the marine boundary layer included chemical composition; number size distribution; and light scattering, hemispheric backscattering, and absorption coefficients. In addition, optical depth and vertical profiles of aerosol 180 deg backscatter were measured. Aerosol within the ACE Asia study region was found to be a complex mixture resulting from marine, pollution, volcanic, and dust sources. Presented here as a function of air mass source region are the mass fractions of the dominant aerosol chemical components, the fraction of the scattering measured at the surface due to each component, mass scattering efficiencies of the individual components, aerosol scattering and absorption coefficients, single scattering albedo, Angstrom exponents, optical depth, and vertical profiles of aerosol extinction. All results except aerosol optical depth and the vertical profiles of aerosol extinction are reported at a relative humidity of 55 +/- 5%. An over-determined data set was collected so that measured and calculated aerosol properties could be compared, internal consistency in the data set could be assessed, and sources of uncertainty could be identified. By taking into account non-sphericity of the dust aerosol, calculated and measured aerosol mass and scattering coefficients agreed within overall experimental uncertainties. Differences between measured and calculated aerosol absorption coefficients were not within reasonable uncertainty limits, however, and may indicate the inability of Mie theory and the assumption of internally mixed homogeneous spheres to predict absorption by the ACE Asia aerosol. Mass scattering efficiencies of non-sea salt sulfate aerosol, sea salt, submicron particulate organic matter, and dust found for the ACE Asia aerosol are comparable to values estimated for ACE 1, Aerosols99, and INDOEX. Unique to the ACE Asia aerosol was the large mass fractions of dust, the dominance of dust in controlling the aerosol optical properties, and the interaction of dust with soot aerosol.

Quinn, P. K.↗

Mantle Metasomatism in Mars: Evidence from Bulk Chemical Compositions of Martian Basalts

Bulk compositions of martian meteorite basalts suggest that they formed from a highly depleted mantle that was variably metasomatised and enriched in incompatible elements. These results are consistent with radio-isotope results. Bulk chemical compositions of basaltic rocks retain clues and tracers to their origins and histories. Interpretations of bulk compositions are not so straight-forward as once envisioned, because real-world magmatic processes can be far from theoretical simple models like one-stage partial melting or closed-system fractional crystallization. Yet, bulk chemistry can shed a broad (if dim) light on Martian basalt petrogenesis that complements the sharply focussed illumination of radio-isotope systematics.

Treiman, A. H.↗

Unusual chemical compositions of noctilucent-cloud particle nuclei

Two sounding rocket payloads were launched from the ESRO range in Sweden during a noctilucent cloud display. Large numbers of submicron particles were collected, most of which appear to be made up of a high density material coated with a low density material. Typical electron micrographs are shown. Particle chemical compositions have been measured by use of dispersive X-ray analysis equipment attached to an electron microscope and have revealed that most of the high density particle nuclei have atomic weights greater than iron.

Hemenway, C. L.↗

Chemical compositions of primitive solar system particles

Chemical studies of micrometeorites are of fundamental importance primarily because atmospheric entry selection effects (such as destruction of friable objects) are less significant than those for conventional meteorites. As a result, particles that have experienced very little postaccretional processing have a significant chance of surviving the Earth encounter and subsequent collection. Thus, chemical analyses of these relatively unaltered micrometeorites may lead to a better understanding of the compositions of the most primitive materials in the solar system and thereby constrain the conditions (physical and chemical) that existed in the early solar nebula. Micrometeorites have been collected from the stratosphere, polar ices, and ocean sediments, but the stratospheric collection is the best source for the most unaltered material because they are small and are not heated to their melting points. Despite the fact that the stratospheric micrometeorites have masses in the nanogram range, a variety of microanalytical techniques have been applied to bulk chemical analyses with part-per-million sensitivity. In some cases, multi-disciplinary studies (e.g., chemistry and mineralogy) have been performed on individual particles. The first-order conclusion is that the chondrite-like particles are chemically similar to carbonaceous chondrites but in detail are distinct from members of the conventional meteorite collection. The purpose of this paper is to provide an overview of the results to date and identify important areas for further study.

Sutton, Steve R.↗

Chemical compositions of some soils and rock types from the Apollo 15, 16, and 17 lunar sites

The major and minor element compositions of three Apollo 15 mare basalts, four Apollo 16 breccias, one soil, three Apollo 17 soils, one mare basalt, and one breccia have been determined by semimicro combined atomic absorption and colorimetric spectrophotometries. A discussion regarding analysis of small subsamples of coarse-grained lunar materials, such as certain Apollo 15 and 17 basalts, is given in which the suggestion is made that analytical methods designed to determine the bulk 'representative' chemical composition as well as the presence and extent of specimen heterogeneity are fundamentally necessary for a more complete understanding of genesis and history of lunar materials.

Nava, D. F.↗

Chemical composition of HAL, an isotopically-unusual Allende inclusion

Samples of hibonite, black rim, and portions of friable rim from an unusual Allende inclusion, named HAL, were analyzed by INAA and RNAA for 37 major, minor, and trace elements. An unusually low amount of Ce was found in HAL, although it otherwise was highly enriched in REE compared to C1 chondrites. HAL is also depleted in Sr, Ba, U, V, Ru, Os, and Ir relative to other refractory elements. It is concluded that the distribution of REE between hibonite and rims was established when hibonite and other refractory minerals were removed at slightly different temperatures from a hot, oxidizing gas in which they previously coexisted as separate grains. Possible locations for the chemical and mass dependent isotopic fractionation are considered to be in ejecta from the low temperature helium-burning zone of a supernova and in the locally oxidizing environment generated by evaporation of interstellar grains of near-chondritic chemical composition.

Davis, A. M.↗

The surface chemical composition of lunar samples and its significance for optical properties

The surface Fe, Ti, Ca, and Si concentrations in a variety of soil and rock samples from all the Apollo sites are determined using an Auger spectrometer plus a single-pass cylindrical-mirror analyzer with a standard 15-stage BeCu electron multiplier. It is found that there are no great differences between the surface and bulk concentrations of any of the four elements in the rock samples, but the surface Fe and Ti concentrations in soil samples are higher than the bulk concentrations. Results are also reported for solar-wind simulation experiments in which a pulverized rock sample was bombarded with 2-keV alpha-particles corresponding to about a 30,000-yr dose of the solar-wind proton component. These results indicate that the chemical change induced on the surface of a rock powder by positive-ion bombardment is similar to the change from bulk to surface chemical composition in lunar soil samples. A clear correlation is observed between the surface Fe concentration and albedo of the soil samples.

Gold, T.↗

The Chemical Composition and Gas-to-Dust Mass Ratio of Nearby Interstellar Matter

We use recent results on interstellar gas toward nearby stars and interstellar by-products within the solar system to select among the equilibrium radiative transfer models of the nearest interstellar material presented in Slavin & Frisch. For the assumption that O/H - 400 parts per million, models 2 and 8 are found to yield good fits to available data on interstellar material inside and outside of the heliosphere, with the exception of the Ne abundance in the pickup ion and anomalous cosmic-ray populations. For these models, the interstellar medium (ISM) at the entry point to the heliosphere has n(H(sup 0)) = 0.202-0.208/cu cm, n(He(sup 0) = 0.0137-0.0152/cu cm, and ionizations X(H) = 0.29-0.30, X(He) = 0.47-0.51. These best models suggest that the chemical composition of the nearby ISM is approx.60%-70% subsolar if S is undepleted. Both H(0) and H(+) need to be included when evaluating abundances of ions found in warm diffuse clouds. Models 2 and 8 yield an H filtration factor of approx.0.46. Gas-to-dust mass ratios for the ISM toward epsilon CMa are R(sub gd) = 178-183 for solar abundances of Holweger or R(sub gd) = 611-657 for an interstellar abundance standard 70% solar. Direct observations of dust grains in the solar system by Ulysses and Galileo yield R(sub gd) appr0x. 115 for models 2 and 8, supporting earlier results (Frisch and coworkers). If the local ISM abundances are subsolar, then gas and dust are decoupled over small spatial scales. The inferred variation in R(sub gd) over parsec length scales is consistent with the fact that the ISM near the Sun is part of a dynamically active cluster of cloudlets flowing away from the Sco-Cen association. Observations toward stars within approx.500 pc show that R(sub gd) correlates with the percentage of the dust mass that is carried by iron, suggesting that an Fe-rich grain core (by mass) remains after grain destruction. Evidently large dust grains (>10(exp -13) g) and small dust grains (<10(exp -13) g) are not well mixed over parsec length spatial scales in the ISM. It also appears that very small C-dominated dust grains have been destroyed in the ISM within several parsecs of the Sun, since C appears to be essentially undepleted. However, if gas-dust coupling breaks down over the cloud lifetime, the missing mass arguments applied here to determine R(sub gd) and dust grain mineralogy are not appropriate.

Frisch, Priscilla C.↗

Computer program determines chemical composition of physical system at equilibrium

FORTRAN 4 digital computer program calculates equilibrium composition of complex, multiphase chemical systems. This is a free energy minimization method with solution of the problem reduced to mathematical operations, without concern for the chemistry involved. Also certain thermodynamic properties are determined as byproducts of the main calculations.

Kwong, S. S.↗

Variations in chemical composition of Apollo 15 mare basalts

Chemical analyses of 30 different Apollo 15 mare basalts were examined to evaluate the effects of closure on the pearson moment correlation coefficient. It is shown possible to describe the Apollo 15 mare basalts in terms of an opaque, an olivine/pyroxene, an anorthite, and a KREEP component, if significant correlations are identified using the expected correlations as null values. Using Q-mode cluster analysis and nonlinear mapping, it is possible to recognize three groups of the mare basalts, groups 1 and 2 belonging to the olivine normative basalt cluster and group 3 to the quartz normative cluster.

Butler, J. C.↗