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511.
Robert N. Clayton Glenn J. MacPherson Ian D. Hutcheon Andrew M. Davis Lawrence Grossman Toshiko K. Mayeda Carol Molini-Velsko John M. Allen Ahmed El Goresy 《Geochimica et cosmochimica acta》1984,48(3):535-548
We have discovered two FUN inclusions, CG-14 and TE, among a group of five forsterite-rich inclusions in Allende, two of which are described for the first time herein. All five consist of euhedral forsterite and spinel crystals poikilitically enclosed by fassaite. Forsterite and spinel are usually segregated from one another, sometimes into a spinel-rich mantle and a forsterite-rich core. Some inclusions contain vesicles, indicating that they were once molten. The crystallization sequence inferred from textures is: spinel, forsterite, fassaite and, finally, Mg-rich melilite. One concentrically-zoned inclusion contains melilite in its mantle whose composition lies on the opposite side of the liquidus minimum in the melilite binary from that in its core. This suggests that segregation of forsterite from spinel in all of these inclusions could be due to volatilization of MgO and SiO2 relative to Al2O3 and CaO from the outsides of droplets. CG-14 is relatively uniformly enriched in refractory elements relative to Cl chondrites by a factor similar to that for Ca-, Al-rich coarse-grained inclusions except for Ca, Al and Hf which are unusually low. No Ce anomaly such as found in FUN inclusions Cl and HAL is present in CG-14. Whole-rock samples of CG-14 and TE are more strongly mass-fractionated in oxygen relative to “normal” Allende inclusions than the FUN inclusion EK 1-4-1 and less so than Cl. Relative to bulk Allende, both inclusions have strongly massfractionated magnesium and silicon and 25Mg excesses or deficits of 24Mg or 26Mg. CG-14 has a 29Si excess or a deficit of 28Si or 30Si. Volatilization loss cannot be responsible for the magnesium and silicon isotope fractionations, as this would require prohibitively large mass loss from these magnesium-rich inclusions. The remarkable similarity in textures between FUN and non-FUN inclusions implies similar thermal histories, arguing against different rates of evaporative loss of major elements. Sputtering alone may be insufficient to account for the magnitude and direction of oxygen isotope fractionation in FUN inclusions. 相似文献
512.
Georges Calas Gordon E. Brown Jr. Glenn A. Waychunas Jacqueline Petiau 《Physics and Chemistry of Minerals》1987,15(1):19-29
Selected results of x-ray absorption spectroscopy (XAS) studies of amorphous silicates and minerals are presented in order to show their utility in providing short-and, in certain cases, medium-range structural and bonding information for cations and anions. EXAFS and XANES studies of amorphous silicates are reviewed with the objective of illustrating variations in structural environments of the various types of glass-forming cations, including Si, Al, Na, K, Ca, Ti, Fe, Yb, and U. Al is shown to occur in tetrahedral coordination in all aluminosilicate glasses examined, including peraluminous compositions. The weakly bonded Na and Ca cations are shown to occur in sites with observed coordination numbers (ranging from 6 to 7) and distances similar to those predicted by molecular dynamics simulations. Elements like Ti, which form bonds of intermediate strength, may show some order beyond the first coordination shell at low concentrations in silicate glasses. EXAFS studies of Yb and U in silicate glasses at trace to minor concentration levels provide unique structural information about the environments of these cations. K-edges and XANES of transition element sulfides, third-row tetrahedral oxyanions, and oxygen in minerals are interpreted in terms of band theory or molecular orbital theory. 相似文献
513.
514.
Miryam Bar-Matthews Ian D Hutcheon Glenn J MacPherson Lawrence Grossman 《Geochimica et cosmochimica acta》1982,46(1):31-41
A corundum-hibonite inclusion, BB-5, has been found in the Murchison carbonaceous chondrite. This is the first reported occurrence of corundum as a major phase in any refractory inclusion, even though this mineral is predicted by thermodynamic calculations to be the first condensate from a cooling gas of solar composition. Ion microprobe measurements of Mg isotopic compositions yield the unexpected result for such an early condensate that 26Mg excesses are small: δN26Mg = 7.0 ± 1.6%. for hibonite and 5.0 ± 4.8%. for corundum, despite very large ratios, 130 and 2.74 × 104, respectively. Within the errors, δN26Mg does not vary over this exceedingly large range of ratios. The extreme temperature required to melt this inclusion makes a liquid origin unlikely, except possibly by hypervelocity impact involving refractory bodies. If, instead, BB-5 is a direct gas-solid condensate, textural evidence implies that corundum formed first and later reacted to produce hibonite. In this model, BB-5's uniform enrichment in 26Mg must be a characteristic of the reservoir from which it condensed. Because severe difficulties are encountered in making such a reservoir by prior decay of 26Al, nebular heterogeneity in magnesium isotopic composition is a preferred explanation. 相似文献
515.
Thomas H. Shipley Jill M. Whitman Frederick K. Duennebier Lisa D. Petersen 《Earth and Planetary Science Letters》1983,64(2):257-275
An interpretation of the seismic stratigraphy and sedimentation history of the East Mariana Basin has been made using recently collected seismic reflection and refraction data. This Mesozoic(?) age basin, between the Marshall Islands and the Mariana Trench, is subdivided into three regions. The central region with about 1000 m of sediment probably records Jurassic to Late Cretaceous sedimentation of a pelagic biogenic and clay-rich section overlain by a thick section of mainly Cenozoic carbonates shed from nearby volcanic platforms. A western region is characterized by a thinner sediment cover and a shallower acoustic basement with a similar sedimentation history except that the upper section is thinner as a consequence of fewer nearby volcanic highs. Extensive Late Cretaceous mid-plate volcanics apparently masks the lower section and forms acoustic basement. The shallower eastern region (east of 157.5°E) contains WNW-trending ridges which may be either fracture zones or high-amplitude abyssal hills. The sedimentation appears controlled by the same factors as in the other regions but the area was bypassed by most Cenozoic basin-filling turbidites because of its elevation.The isostatistically corrected basement depths between the three regions suggest that the crust in the east may be substantially younger than in the rest of the East Mariana Basin, perhaps Cretaceous in age. This requires the existence of a tectonic boundary within the basin. 相似文献
516.
Bio-controlled thermostasis involving the sulfur cycle 总被引:4,自引:0,他引:4
Glenn E. Shaw 《Climatic change》1983,5(3):297-303
The Gaia hypothesis proposed by Lovelock and Margulis presumes the existence of an unspecified biological means of ameliorating
climate that has operated since the emergence of life 3500 Myr ago: Recently it was suggested that the mechanism of thermostasis
may involve biospheric cycling of atmospheric carbon dioxide.
We suggest an alternative hypothesis of biothermostasis operating through the sulfur cycle, rather than the carbon cycle.
The mechanism would operate by altering planetary albedo through the selective creation of biospheric organic sulfide gases
which go on to metamorphize into submicron particles and introduce cooling. In contrast to the carbon-cycle mechanism, sulfur-based
cooling would have the ability to ameliorate climate well into the future, in principle over stellar Main Sequence time intervals.
The main feature of interest is that the S cycle represents a particularly favorable thermodynamic pathway, involving three
to four orders of magnitude less mass of active material cycled through the biospheric-atmospheric system (in response to
a given temperature-imposed stress) than would be the case for a greenhouse gas hypothesis.
There is no evidence that the suggested biospheric controlled particle-albedo change mechanism is actually operating, but
we speculate that the probability of its rising importance and perhaps eventual dominance will improve when the partial pressure
of atmospheric CO2 drops low enough to impose stress on metabolic processes. The intriguing thing about the process is its extremely high efficiency. 相似文献
517.
518.
The regional patterns of change of temperature and rainfall that might accompany a global warming due to increased carbon
dioxide can be studied by experiments with theoretical models of the climate system, by reconstructing the climates of past
warm epochs, and by determining the anomalies of temperature and precipitation that prevailed during years or seasons when
the Arctic region was unusually warm. The current study pursues the last course, making use of the northern hemisphere meteorological
data record for the period 1931–1978. Hemispheric maps of anomalies of both temperature and precipitation are presented for
the 10 warmest Arctic seasons and years, and for differences between the 5 warmest and 5 coldest consecutive Arctic winters.
Wintertime anomalies are generally greatest and dominate in determining the annual averages. The hemispheric temperature anomalies
for these data sets are similar to those determined earlier by the first author (Williams, 1980) using 1900–1969 data, but
the precipitation anomalies (for North America alone) show more variation, partly due to the method of computing the anomalies.
Work reported here begun while a visitor to the National Center for Atmospheric Research.
The National Center for Atmospheric Research is sponsored by the National Science Foundation. 相似文献
519.
Johanna Marin-Carbonne Kevin D. McKeegan Andrew M. Davis Glenn J. MacPherson Ruslan A. Mendybaev Frank M. Richter 《Meteoritics & planetary science》2023,58(4):546-571
Oxygen, magnesium, and silicon isotopic abundances in Vigarano 1623-5 were studied using secondary ion mass spectrometry to investigate correlations between isotopic and petrologic properties of this unique forsterite-bearing FUN inclusion. Vigarano 1623-5 displays large, correlated mass-dependent fractionation effects, tightly linked to mineralogy within distinct petrologic units of the inclusion. The pyroxene-rich and melilite-rich interior parts of the inclusion display highly mass-fractionated isotopic compositions of oxygen, magnesium, and silicon, consistent with Rayleigh distillation during evaporation of a melt with initial oxygen composition close to a solar composition. However, the chemical composition, enriched in magnesium and silicon, suggests a precursor already fractionated by prior melt evaporation. A discontinuous igneous rim was produced by a flash-melting event followed by isotopic exchange in the rim melilite with planetary-like oxygen, mechanical fragmentation, and reassembly with an accretionary rim of heterogeneous materials. Al-rich minerals in 1623-5 show evidence for having crystallized with live 26Al but at less than the “canonical” level of most CV calcium-aluminum-rich inclusions. However, well-defined 26Al-26Mg isochrons are not found and temporal implications are ambiguous. 相似文献
520.
Suzanne B. Bricker Fred T. Mackenzie Jill S. Baron Jason R. Price 《Aquatic Geochemistry》2014,20(2-3):81-86
This special volume of aquatic geochemistry is dedicated to the memory of Owen Peterson Bricker III (1936–2011) and serves as a tribute to his life and career. Owen had a distinguished and productive research career in both academics at Johns Hopkins University (Fig. 1) and as a public servant with the Maryland Geological Survey, the US Environmental Protection Agency, and the US Geological Survey. He was a pioneer and leader in aqueous geochemistry, who applied a study approach that quantified mineral weathering reactions and equilibrium thermodynamic relations to better understand the chemical evolution of stream water in small watersheds. He will be especially remembered for his efforts to establish rigorous field studies in small catchments around the United States as a means of quantifying the sources of acid-neutralizing capacity that affect the chemical status and biological health of natural waters. Fig. 1
Owen in a Johns Hopkins University laboratory in the early years (~1965, note the tie!) 相似文献