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At least 163 records · Page 9

Oxygen isotope fractionation between analcime and water - An experimental study

The oxygen isotope fractionation between analcime and water is studied to test the feasibility of using zeolites as low-temperature thermometers. The fractionation of oxygen isotopes between natural analcime and water is determined at 300, 350, and 400 C, and at fluid pressures ranging from 1.5 to 5.0 kbar. Also, isotope ratios for the analcime framework, the channel water, and bulk water are obtained. The results suggest that the channel water is depleted in O-18 relative to bulk water by a constant value of about 5 percent, nearly independent of temperature. The analcime-water fractionation curve is presented, showing that the exchange has little effect on grain morphology and does not involve recrystallization. The exchange is faster than any other observed for a silicate. The exchange rates suggest that zeolites in active high-temperature geothermal areas are in oxygen isotopic equilibrium with ambient fluids. It is concluded that calibrated zeolites may be excellent low-temperature oxygen isotope geothermometers.

Karlsson, Haraldur R.↗

Isotope mass fractionation during evaporation of Mg2SiO4

Synthetic forsterite (Mg2SiO4) was partially evaporated in vacuum for various durations and at different temperatures. The residual charges obtained when molten Mg2SiO4 was evaporated to 12 percent of its initial mass were enriched in heavy isotopes by about 20, 30, and 15 per mil/amu for O, Mg, and Si, respectively, whereas solid forsterite evaporated to a similar residual mass fraction showed negligible fractionations. These results imply that calcium and aluminum-rich refractory inclusions in carbonaceous chondrites must have been at least partially molten in the primordial solar nebula if the observed large mass fractionation effects were caused by evaporation processes in the nebula.

Davis, Andrew M.↗

The least-squares mixing models to generate fraction images derived from remote sensing multispectral data

Constrained-least-squares and weighted-least-squares mixing models for generating fraction images derived from remote sensing multispectral data are presented. An experiment considering three components within the pixels-eucalyptus, soil (understory), and shade-was performed. The generated fraction images for shade (shade image) derived from these two methods were compared by considering the performance and computer time. The derived shade images are related to the observed variation in forest structure, i.e., the fraction of inferred shade in the pixel is related to different eucalyptus ages.

Shimabukuro, Yosio Edemir↗

Formation of Apollo 14 aluminous mare basalts by replenishment fractional crystallization and assimilation of precursor crust

Apollo 14 aluminous mare basalts (AMB) have been the subject of considerable controversy. These basalts were divided into 5 distinct groups on the basis of RE and HFS element abundances. The groups are similar in major element compositions but display an 8 fold variation in REE abundances. Open-system processes were explored which are common on Earth: combined replenishment fractional crystallization (RFC); and assimilation fractional crystallization (AFC), where the assimilant is a partial melt of precursor crust. RFC often produces decoupled major and trace element variations, while AFC can produce significant variation in incompatible trace element ratios. A model was envisioned by which magmas of Group 5 composition were emplaced in shallow chambers. The Apollo 14 AMB was modeled by RFC using a parental magma of Group 5 composition with the fractionating assemblage consisting of 60 pct. Px, 30 pct. Plag, and 3 pct. Il.

Dickinson, Tammy L.↗

Fractionation of terrestrial neon by hydrodynamic hydrogen escape from ancient steam atmospheres

Atmospheric neon is isotopically heavier than mantle neon. By contrast, nonradiogenic mantle Ar, Kr, and Xe are not known to differ from the atmosphere. These observations are most easily explained by selective neon loss to space; however, neon is much too massive to escape from the modern atmosphere. Steam atmospheres are a likely, if intermittent, feature of the accreting Earth. They occur because, on average, the energy liberated during accretion places Earth above the runaway greenhouse threshold, so that liquid water is not stable at the surface. It is found that steam atmospheres should have lasted some ten to fifty million years. Hydrogen escape would have been vigorous, but abundant heavy constituents would have been retained. There is no lack of plausible candidates; CO2, N2, or CO could all suffice. Neon can escape because it is less massive than any of the likely pollutants. Neon fractionation would have been a natural byproduct. Assuming that the initial Ne-20/Ne-22 ratio was solar, it was found that it would have taken some ten million years to effect the observed neon fractionation in a 30 bar steam atmosphere fouled with 10 bars of CO. Thicker atmospheres would have taken longer; less CO, shorter. This mechanism for fractionating neon has about the right level of efficiency. Because the lighter isotope escapes much more readily, total neon loss is pretty minimal; less than half of the initial neon endowment escapes.

Zahnle, K.↗

A comparison of solar wind and estimated solar system xenon abundances - A test for solid/gas fractionation in the solar nebula

The solar Xe elemental abundance is determined here using solar wind measurements from lunar ilmenites which are normalized to Si by spacecraft data. The results are compared with estimated abundances assuming no fractionation. When corrected for solar wind/photospheric fractionation, the Xe-130 abundance given by surface layer oxidation of ilmenite from solid 71501 exposed within the last 200 m.y. is 0.24 +/- 0.09 normalized to Si = 10 exp 6. This is indistinguishable from estimates made assuming no solid/gas fractionation. Results from breccia 79035 ilmenite exposed at least 1 Gyr ago indicate that the solar wind Xe flux may have been significantly higher relative to other noble gases, perhaps due to more efficient Xe ionization. If this is true, fluxes of C and S, which have first ionization potentials similar to Xe, should also be higher in the ancient solar wind from the same time period.

Wiens, Roger C.↗

Rock fraction effects on the interpretation of microwave emission from soils

The effect of the rock fraction of soil on emissivity is presently investigated through a combination of laboratory dielectric measurements and field observation of emissivity from soils with and without rocks. The rock fraction reduced the range of emissivity; beyond this, it appears to be important only in determining the moisture in the soil component. Data gathered at 6 cm indicate that the presence of rocks renders this and shorter wavelengths useless as soil-moisture sensors. Modeling of the 21-cm case suggest that rock-fraction effects on soil dielectric properties can be compensated for by the greater surface roughness.

Jackson, Thomas J.↗

Impact glasses from the less than 20-micrometer fraction of Apollo 17 soils 72501 and 78221

The chemical compositions of microscopic glasses produced during meteoroid impacts on the lunar surface provide information regarding the various fractionation processes that accompany these events. To learn more about these fractionation processes, we studied the compositions of submicrometer glass spheres from two Apollo 17 sampling sites using electron microscopy. The majority of the analyzed glasses show evidence for varying degrees of impact-induced chemical fractionation. Among these are HASP glasses (high-Al, Si-poor), which are believed to represent the refractory residuum left after the loss of volatile elements (e.g., Si, Fe, Na) from the precursor material. In addition to HASP-type glasses, we also observed a group of volatile-rich, Al-poor (VRAP) glasses that represent condensates of vaporized volatile constituents, and are complementary to the HASP compositions. High-Ti glasses were also found during the course of this study, and are documented here for the first time.

Norris, John A.↗

Fractionation of CO in the diffuse clouds toward Zeta Ophiuchi

An analysis of CO A-X bands in diffuse clouds toward Zeta Ophiuchi is presented. The results provide isotopic ratios that constitute the strongest observational evidence for highly localized isotopic fractionation of CO in diffuse portions of an interstellar cloud. The value of the fractionation implies that selective photodissociation is the controlling influence of the fractionation. The molecule's excitation temperature is discussed and a lower limit to the O-16/O-18 ratio is provided. The absence of CO lines from the gas that provides broad CH+ and CH lines commonly attributed to warm gas behind a shock front is addressed.

Sheffer, Yaron↗

Mineral equilibrium in fractionated nebular systems

We investigated the equilibrium mineral assemblages in chemically fractionated nebular systems, using a computer routine that finds the set of minerals and gases which minimizes the Gibbs free energy of a system with stipulated elemental abundances. Diagrams are presented showing the equilibrium mineralogy, as a function of temperature (400-2300 K), for unfractionated solar material and five fractionated systems. The fractionated systems were defined by mixing, in various proportions, the following four volatility components that solar material can be divided into: refractory dust, carbonaceous matter, ices, and H2 gas. Dust enrichment is seen to increase temperatures of condensation/evaporation and the Fe(2+) content of mafic minerals and to permit existence of stable melt phases. Enrichment of dust and organic matter produces mineral assemblages that are similar in many ways to those of enstatite chondrites, but with mafic minerals that are far more reduced than those in primitive enstatite chondrites. Enrichment of dust, organics, and ices leads to highly ferrous mineralogies even at the highest temperatures but does not predict the stability of hydrous phases above about 450 K.

Wood, John A.↗

Petrogenesis of Apollo 12 mare basalts. Part 1: Multiple melts and fractional crystallization to explain olivine and ilmenite basalt compositions

Mare basalts returned by the Apollo 12 mission have been divided into 4 groups on the basis of mineralogy and whole-rock chemistry: olivine basalts; pigeonite basalts; ilmenite basalts; and feldspathic basalts. James and Wright and Rhodes et al. concluded that the olivine and pigeonite groups were co-magmatic and that the within group variations are due to fractional crystallization of olivine and minor Cr-spinel, with pigeonite replacing olivine in the pigeonite basalts. Rhodes et al. concluded that the parental compositions for these suites were probably represented by the vitrophyres, and the olivine basalts are comprised essentially of cumulates and the pigeonites of evolved end-members. However, Neal et al. have demonstrated, using trace-element considerations, that the Apollo 12 olivine and pigeonite suites are not related. The ilmenite basalts were studied extensively by Dungan and Brown who noted that both cumulates and evolved fractionates were present within this group. In their modeling, Dungan and Brown used the vitrophyre compositions as parents. Neal et al. demonstrated that the feldspathic suite was probably comprised of only one member - 12038. Herein, the ilmenite and olivine basalts are demonstrated to be the products of several non-modal partial melting events of a single source followed by closed-system fractional crystallization.

Neal, Clive R.↗

Impact glasses from the ultrafine fraction of lunar soils

The chemical compositions of microscopic glasses produced during meteoroid impacts on the lunar surface provide information regarding the various fractionation processes which accompany these events. To learn more about these fractionation processes, we studied the compositions of submicrometer glass spheres from two Apollo 17 sampling sites using electron microscopy. The majority of the analyzed glasses show evidence for varying degrees of impact induced chemical fractionation. Among these are HASP glasses (High-Al, Si-Poor) which are believed to represent the refractory residuum left after the loss of volatile elements (e.g. Si, Fe, N) from the precursor material. In addition to HASP-type glasses, we also observed a group of VRAP glasses (volatile-rich, Al-poor) that represent condensates of vaporized volatile constituents and are complementary to the HASP compositions. High-Ti glasses were also found during the course of the study, and are documented here for the first time.

Norris, J. A.↗

Low-energy ion implantation: Large mass fractionation of argon

The isotropic signatures of noble gases in the atmospheres of the Earth and other planets are considerably evolved when compared to signatures observed in the solar wind. The mechanisms driving the evolution of planetary volatiles from original compositions in the solar accretion disk are currently poorly understood. Modeling of noble-gas compositional histories requires knowledge of fractionating processes that may have operated through the evolutionary stages. Since these gases are chemically inert, information on noble-gas fractionation processes can be used as probes. The importance of understanding these processes extends well beyond 'noble-gas planetology.' Trapped argon acquired by low-energy implantation (approximately less than 100 eV) into solids is strongly mass fractionated (approximately greater than or equal to 3 percent/amu). This has potential implications for the origin and evolution of terrestrial planet atmospheres.

Ponganis, K. V.↗

Diffusion-controlled magnesium isotopic fractionation of a single crystal forsterite evaporated from the solid state

Though the origin of calcium- and aluminum-rich inclusions (CAI's) in carbonaceous chondrites is till a disputed issue, evaporation is no doubt one of the most important processes for the formation of CAI's in the early solar nebula. The mechanism for production of large isotopic mass fractionation effects in magnesium, silicon, oxygen, and chromium in CAI's can be better understood by examining isotopic fractionation during the evaporation of minerals. New evaporation experiments were performed on single-crystal forsterite. The magnesium isotopic distribution near the evaporating surfaces of the residues using a modified AEI IM-20 ion microprobe to obtain rastered beam depth profiles was measured. A theoretical model was used to explain the profiles and allowed determination of the diffusion coefficient of Mg(++) in forsterite at higher temperatures than previous measurements. The gas/solid isotopic fractionation factor for magnesium for evaporation from solid forsterite was also determined and found to be nearly the same as that for evaporation of liquid Mg2SiO4.

Wang, Jianhua↗

Predicting LANDSAT MSS endmember signatures from corresponding higher resolution TM fraction images

The approach to predicting Landsat Multispectral Scanner System (MSS) endmember signatures from fraction images derived from high resolution Landsat Thematic Mapper (TM) data is presented. The purpose, conducted in the Mogi-Guacu study site located in Sao Paulo State, Brazil, was to determine if information derived from a mixture model applied to higher resolution TM data could serve as ground truth for the lower resolution MSS sensor. The Constrained Least Squares (CLS) method was used to generate vegetation, soil, and shade fraction images from the TM data. The resulting images were then used to estimate the endmember spectral response for MSS data by regressing each MSS spectral channel against the corresponding proportion values estimated for the same resolution cells from the TM mixture model. The evaluation of the predicted signatures was performed by comparing the corresponding fraction images derived from both the MSS and TM data acquired on 14 Sep. 1986. The techniques serves as a potential tool for integrating information in global studies where remote sensors with different spectral and spatial resolutions were used.

Shimabukuro, Yosio E.↗

First observation of a mass independent isotopic fractionation in a condensation reaction

Thiemens and Heidenreich (1983) first demonstrated that a chemically produced mass independent isotopic fractionation process could produce an isotopic composition which is identical to that observed in Allende inclusions. This raised the possibility that the meteoritic components could be produced by chemical, rather than nuclear processes. In order to develop a mechanistic model of the early solar system, it is important that relevant reactions be studied, particularly, those which may occur in the earliest condensation reactions. The isotopic results for isotopic fractionations associated with condensation processes are reported. A large mass independent isotopic fractionation is observed in one of the experiments.

Thiemens, M. H.↗

Mars atmospheric loss and isotopic fractionation by pick-up-ion sputtering and photochemical escape

We examine the effects of loss of constituents of the Martian atmosphere due to sputtering by solar-wind pick-up ions and photochemical escape during the last 3.8 billion years. Sputtering is capable of efficiently removing species from the upper atmosphere to space, including the light noble gases; nitrogen and oxygen are removed by both sputtering ad photochemical processes. Due to diffusive separation (by mass) above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species, with the lighter isotope being preferentially lost. This allows current measurements of the isotopic ratios to be used as a measure of the atmospheric evolution as integrated over geologic time. For carbon and oxygen, isotopic fractionation is buffered by exchange of atmospheric species with non-atmospheric reservoirs of CO2 and H2O. This allows us to determine the size of the non-atmospheric reservoirs which are capable of mixing with the atmosphere; these reservoirs can be CO2 absorbed in the regolith and/or H2O in the polar ice caps. Such an exchangeable reservoir is required in order to keep the fractionation of the atmospheric gases as low as is observed.

Jakosky, B. M.↗

(H2)2 mole-fraction altitude profile in the atmosphere of Jupiter: A computational study

The mole fraction x(sub 2) of (H2)2 in equilibrium mixture with H2 under the atmospheric conditions of Jupiter is evaluated from the dimerization equilibrium constant calculated by quantum-chemical treatments and also from the Lennard-Jones potential. The treatments are of an ab initio type with the second and fourth order Moller-Plesset perturbation techniques and a basis set superposition error evaluation. The computed dimerization equilibrium constant is combined with observed height profiles of temperature and pressure. In six treatments considered it is found that the mole fraction decreases with increasing height. Various approximations suggest the dimeric mole fraction at the Jupiter 1 atm pressure level between 0.04 and 1.06%.

Slanina, Zdenek↗