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At least 217 records · Page 12

Noble gas trapping and fractionation during synthesis of carbonaceous matter

An investigation of noble gas entrapment during synthesis of carbonaceous, macromolecular, and kerogen-like substances is presented. High molecular weight organic matter synthesized in aqueous condensation reactions contained little gas, and the composition was consistent with fractionation due to noble gas solubility in water; however, propane soot produced during a modified Miller-Urey experiment in an aritificial gas mixture contained high concentrations of trapped noble gases that displayed strong elemental fractionation from their reservoirs. It is concluded that theses experiemnts show that processes exist for synthesis of carbonaceous carriers that result in high noble gas concentrations and strong elemental fractionation at temperatures well above those required by absorption to achieve similar effects.

Frick, U.↗

Trace elements in ocean ridge basalt glasses - Implications for fractionations during mantle evolution and petrogenesis

Seven documented and fresh glassy selvages from ocean floor basalt pillows were analyzed for trace elements including Ag, Au, Bi, Br, Ni, Pd, and Zn using radiochemical activation analysis. Glasses from DSDP leg 24, site 238 in the Indian Ocean have a trace element pattern which reflects secondary processes at a shallow depth. Chemical fractionations in petrogenesis of tholeiitic basalts indicate that (Ir, Os), Au, Pd, Ni, and Re are strongly fractionated in igneous processes; the unfractionated chondritic mantle pattern thus imposes constraints on mantle evolution models. Finally, the limited Rb/Cs fractionation in oceanic tholeiites reflects the low abundance of volatiles and hydrous silicates in normal ocean ridge basalts.

Hertogen, J.↗

Single isotope fractionation of (16)O(-) implications for early history of solar system

Chemical fractionation processes are investigated with emphasis on selective single isotope fractionation in polyisotopic systems, particularly in oxygen. The related temperature parameters of meteoritic condensates and of their source medium are investigated by a thermometric method that is independent of assumptions regarding temperatures and pressures in the solar nebula. The crucial nonlinear chemical fractionation of O-16 was demonstrated experimentally. The effect was achieved in condensed CO2 formed from CO with C-12 O-16 selectively excited by H Ly alpha. The effect was verified by mass spectrometric measurements. The meteorite paleotemperature estimates were advanced from defining only thermal exposure to evaluating time and temperature independently. Grain temperatures at condensation of refractory inclusion materials are indicated to be less than 900 K in agreement with radiation temperature considerations and observations in circumstellar dust shells.

Arrhenius, G.↗

Fractionation of siderophiles in cosmic spherules and its implications

Fractionation of siderophiles between metal and silicate phases at different oxygen fugacities was extensively studied. Such data could be applied to study the fractionation during formation of stony or iron spherules. However another kind of fractionation exists which takes place within the spherules as they are molten and oxidized in the Earth's atmosphere. During this process two phases develop, one oxidized, the other not. Unoxidized phase is the globule described by shape and high Fe and Ni contents. The process of atmospheric melting is dependent on many factors, one of which is the density of the atmosphere. The density profile of the atmosphere is assumed to have remained constant with time, whereas composition has not. Quantitative explanations of depletions or absence of siderophiles in spherules were initiated.

Czajkowski, J.↗

Grain size evolution and fractionation trends in an experimental regolith

The communication of blocky planetary surfaces into fine-grained regoliths was simulated by impacting a fragmental gabbro target 200 times with stainless steel projectiles. It is found that the comminution efficiency of the surfaces changes with time, being highest in the early stages of regolith formation and decreasing gradually. The relationship between mean grain size and cumulative energy is not linear. Individual, fine-grained regolith components can be generated very early from relatively large progenitor fragments without going through intermediate-size fractions. Impact comminution is capable of producing fractionated fines as postulated by Papike et al. (1982). The role of grain-size selective, lateral transport to explain the fractionated nature of lunar regolith fines may have been overestimated in the past.

Horz, F.↗

Zr-Hf-Ta fractionation during lunar evolution

Zr/Hf ratios and other elemental data in 68 samples of various mare basalts, KREEP units, and lunar glasses have been determined using instrumental neutron activation analysis coupled with coincidence-anticoincidence counting for greater precision. The data are presented in order to quantify further the amount of Zr/Hf fractionation that has occurred during primordial crystallization and cumulate remelting or by any other process. Models of Zr-Hf evolution are developed to place additional constraints on the bulk lunar composition and on the effects of minor phases that may be responsible for the observed fractionations. The Hf-Ta fractionation in lunar compositions is also reviewed in order to characterize normal Hf(4+) versus Ta(4+) behavior and to delineate possible effects due to the oxidation of Ta(4+) to Ta(5+) during late-stage ilmenite crystallization.

Hughes, S. S.↗

Isotopic fractionation of Kr and Xe implanted in solids at very low energies

Results on the implantation of Kr and Xe in W under closed system conditions at very low energies (50-500 eV) are reported. Investigation of the fraction of gas trapped as a function of time reveals the existence of competing trapping and release mechanisms, and analysis of recovered trapped gas and residual gas phases shows that both elemental and isotropic fractionation result from these mechanisms. It is determined that the mass dependence for the overall implantation process is at or near m exp 1, with heavier isotopes enriched in the implanted gas. This mass dependence is inferred to result from implantation and a combination of diffusive and gas sputtering release mechanisms. These results reaffirm the conclusion of Bernatowicz and Fahey (1986) that previously observed isotopic fractionation of Kr and Xe in carbonaceous material synthesized in electrical discharges owes its origin to low-energy ion implantation, and also suggest that this process may be relevant to incorporation of noble gases in early solar system materials. The implication of these results for noble gas mass spectrometry are discussed.

Bernatowicz, Thomas J.↗

Numerical analysis of discrete fractional integrodifferential structural dampers

This paper develops solution algorithms enabling the handling of the dynamic response of nonlinear structures contained discretely attached dampers modeled by fractional integrodifferential operators of the Grunwald-Liouville-Riemann type. The development consists of two levels of formulation, namely: (1) numerical approximations of fractional operators and, (2) the establishment of global level implicit schemes enabling the solution to nonlinear structural formulations. To generalize the overall results, error estimates are derived for the fractional operator approximation algorithm. These enable an ongoing optimization of solution efficiency for a given error tolerance. To benchmark the scheme, the results of several numerical experiments are presented. These illustrate the numerical characteristics of the overall formulation.

Padovan, Joseph↗

Isotopic fractionation in ozone decomposition

The oxygen isotopic fractionation, which occurs during ozone decomposition, has been determined, complementing earlier studies on the fractionation during ozone formation. Oxygen produced in the decomposition is depleted in heavy isotopes in a mass-independent fashion. The mechanism for the mass-independent effect is unknown, though the fractionation magnitude information is required for modeling the steady-state isotopic composition of stratospheric ozone.

Bhattacharya, S. K.↗

Mole fraction imaging of transverse injection in a ducted supersonic flow

Laser-induced iodine fluorescence has been used to generate two-dimensional images of the mixing characteristics of air injected transversely as underexpanded jets behind a rearward-facing step into a ducted Mach 2 freestream; the images thus obtained were processed digitally in order to yield planar-injectant mole fraction distributions. The resulting planar images represent a three-dimensional data base of the injectant mole fraction distribution throughout the flowfield which is then used to reconstruct images exhibiting mole-fraction distributions normal to the duct. These images furnish a direct representation of the evolution of supersonic mixing along the duct, and facilitate the development of one-dimensional mixing schedules on the basis of the three-dimensional data base.

Abbitt, John D. Iii↗

Volatile fractionation and tektite source material

The arguments used by Love and Woronow (1988) to assess the role played in the origin of bediasites by extensive volatile fractionation are critically examined. Using the ratios of 'refractory' oxides, CaO, Al2O3, and MgO, to the 'volatile' oxides, Na2O and K2O, these authors concluded that vapor fractionation did not play a significant role. In this paper, experimental evidence is presented that shows that the assumption of volatility for the alkali elements (as least with respect to silica) to be not valid under the conditions under which tektites formed. It is shown that the results of vapor fractionation in experiments on glasses of tektite composition are approximately parallel the trends seen in bediasite analysis.

Walter, Louis S.↗

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.↗