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101.
Oxidation of CH4 provides the major source for atmospheric H2 which is removed mainly by reaction with OH. Biological activity at the Earth's surface appears to represent at most a minor sink for H2. Anthropogenic activity is a significant source for both H2 and CO in the present atmosphere and may be expected to exert a growing influence in the future. Models are presented which suggest a rise in the mixing ratio of H2 from its present value of 5.6 × 10?7 to about 1.8 × 10?6 by the year 2100. The mixing ratio of CO should grow from 9.7 × 10?8 to 2.3 × 10?7 over the same time period and there should be a rise in CH4 by about a factor of 1.5 associated with anthropogenically induced reductions in tropospheric OH. 相似文献
102.
Michael A. Cosca Eric J. Essene Michael J. Kunk John F. Sutter 《Contributions to Mineralogy and Petrology》1992,110(2-3):211-225
An 40Ar/39Ar thermochronological investigation of upper greenschist to granulite facies gneiss, amphibolite and marble was conducted in the Central Metasedimentary Belt (CMB), Ontario, to constrain its cooling history. Incremental 40Ar/39Ar release spectra indicate that substantial differential unroofing occurred in the CMB between 1000 and 600 Ma. A consistent pattern of significantly older hornblende and phlogopite 40Ar/3Ar cooling ages on the southeast sides of major northeast striking shear zones is interpreted to reflect late displacement due to extensional deformation. Variations in hornblende 40Ar/39Ar age plateaus exceeding 200 Ma occur over distances less than 50 km with major age discontinuities occurring across the Robertson Lake shear zone and the Sharbot Lake mylonite zone which separate the Sharbot Lake terrane from the Elzevir and Frontenac terranes. Extensional displacements of up to 14 km are inferred between the Frontenac and Elzevir terranes of the CMB. No evidence for significant post argon-closure vertical displacement is indicated in the vicinity of the Perth Road mylonite within the Frontenac terrane. Variations of nearly 100 Ma in phlogopite 40Ar/39Ar plateau ages occur in undeformed marble on either side of the Bancroft Shear Zone. Phlogopites from sheared and mylonitized marble within the shear zone yield 40Ar/39Ar diffusional loss profiles, but have older geologically meaningless ages thought to reflect incorporation of excess argon. By 900 Ma, southeast directed extension was occurring throughout the CMB, possibly initiated along previous zones of compressional shearing. An easterly migration of active zones of extension is inferred, possibly related to an earlier, overall easterly migration of active zones of regional thrusting and easterly migration of an ancient subduction zone. The duration of extensional shearing is not well constrained, but must have ceased before 600 Ma as required by the deposition of overlying undeformed Cambrian and/or Ordovician sedimentary rocks.Contribution No. 481 from the Mineralogical Laboratory, University of Michigan 相似文献
103.
Michael Kohlhase 《Astrophysics and Space Science》1992,198(1):167-172
Guide and examples for users of the SPACEKAP style fileBasic instructions 相似文献
104.
105.
The 0.3–2.6 m reflectance spectra of most mafic and ultramafic assemblages can best be interpreted by considering the spectra as being composed of mafic silicate spectra modified by the presence of opaques, such as ilmenite or magnetite, and plagioclase feldspar. The systematic spectral-compositional relationships for olivine, orthopyroxene, and clinopyroxene have been examined and it has been determined that absorption band wavelength positions are correlated with ferrous iron content. Binary mafic silicate mixtures are generally less well understood, but certain spectral features such as reflectance maxima and minima wavelength positions and absorption band areas can be used to quantify or at least constrain end member abundances and compositions. The addition of opaques to a mafic silicate assemblage lowers overall reflectance and band depths. This differs from the effects of increasing grain size which are to lower overall reflectance but increase band depths. Plagioclase is relatively transparent compared to mafic silicates and must be present in appreciable amounts (tens of percent) to be spectrally detectable. The reflectance spectra of most mafic and ultramafic assemblages are dominated by mafic silicate absorption features and analysis of their spectra on this basis allows constraints to be placed on properties such as end member abundances and compositions. 相似文献
106.
107.
M. R. Ramesh Kumar Y. Sadhuram G. S. Michael L. V. Gangadhara Rao 《Boundary-Layer Meteorology》1990,52(1-2):177-191
The spatial variability of the structure of the lower troposphere over the northwestern Indian Ocean for the period 12th July to 2nd September, 1983 has been studied using upper air data collected during the first scientific cruise of ORV Sagar Kanya.An analysis of thermodynamic structure and kinematics of the marine boundary layer for different zonal and meridional sections revealed the following features: (a) Temperature and humidity inversions were generally absent over the study area except over a few locations in the western region; (b) Large-scale subsidence was found over the central equatorial Indian Ocean; (c) The convective activity over the western Indian Ocean was found to be moderately suppressed as compared to the eastern region; (d) The zonal and meridional components of winds along the equator and 10° N zonal section exhibited a mirror-image-like distribution. 相似文献
108.
Magmatism in the eastern Aleutian Arc: temporal characteristic of igneous activity on Akutan Island 总被引:1,自引:0,他引:1
Jay D. Romick Michael R. Perfit Samuel E. Swanson Robert D. Shuster 《Contributions to Mineralogy and Petrology》1990,104(6):700-721
Lavas from Akutan Island, located in the eastern Aleutian arc at the transition between continental and oceanic crust, show a gradual change in their petrologic and chemical characteristics over the last 4 million years. The oldest lavas exposed on the island, the Hot Springs Bay Volcanics (HSBV), range from magnesian basalt to dacite (45%–62% SiO2). The most mafic basalts contain salitic clinopyroxene, Cr- and Al-rich spinel, and pargasitic amphibole suggesting that they were derived from relatively hydrous magmas at greater pressures than lavas from the younger Akutan Volcanics (AKV) and the modern volcano (MOD). AKV lavas also range between basalt and dacite (46%–63% SiO2), but contain no hydrous phenocrysts and seem to have fractionated within a shallow level magma chamber. Lavas from the modern volcano are andesitic (52%–57% SiO2) and have a mineral assemblage similar to that of AKV lavas of similar composition. With the exception of clinopyroxene and spinel in the most mafic lavas, the compositions of plagioclase (An92?45), olivine (Fo88?51), orthopyroxene (En69?56), and titanomagnetite (15%–21% TiO2) phenocrysts found in these lavas are within the range observed in lavas from other Aleutian volcanoes. Variations in the major element chemistry of the older lavas can be reproduced by fractional crystallization of the observed mineral assemblages, however closed system crystal fractionation models are inadequate to explain the trace element variations. During the last 4 million years, La/Yb ratios have decreased (6.5–3.3 for HSBV lavas and 2.9–1.9 for MOD lavas) whereas Ba/La ratios appear to have increased slightly (37–43 for HSBV and AKV, and 41–45 of MOD). The lower La/Yb ratios of MOD lavas correspond with lower total abundances of the REE and slightly higher Sr and Pb isotopic ratios. The increased87Sr/86Sr ratios and Pb isotopic ratios in the MOD lavas, the less enriched LREE, and the higher Ba/La ratios may result from partial melting of an arc source which has experienced previous melting events but has continued to be contaminated by a component from the subducting slab. It may also indicate a change in the degree of partial melting of the underlying mantle, which corresponds to a different percentage of a slab derived component being incorporated into the overlying mantle. 相似文献
109.
Fresh mid-ocean ridge basalt of varying crystallinity has been powdered and reacted with seawater and an artificial Na-K-Ca-Cl solution at 200–500°C and 500–1000 bar in sealed gold capsules. Water/rock mass ratios of 1–3 were used and durations ranged from 2 to 20 months.These time periods were sufficient for most elements to approach a steady-state concentration in solution which was determined by equilibrium with alteration minerals (Mg, SiO2, SO4), by rate of formation of these minerals (Na, Ca), or by depletion from the rock (K, B, Ba). The resulting solutions closely resemble the brines from the basalt-seawater geothermal system at Reykjanes, Iceland. Mg was almost completely removed from seawater into the alteration products smectite, tremolite-actinolite, or talc. Sulfate also was removed to low concentrations, both by precipitation of anyhydrite and by reduction to sulfide. Net transfer of Na from seawater into solids occurred in most experiments by formation of sodic feldspar and possibly analcime. Sr was removed from seawater in some experiments but showed no change or a small gain in others. SiO2, Ca, K, Ba, B and CO2 were leached from basalt and enriched in solution. SiO2 concentrations were controlled by saturation with quartz at 300°C and above. The principal Ca-bearing phases which formed were anhydrite, the hydrated Ca-silicate truscottite, tremolite-actinolite, and possibly wairakite. No K-rich phases formed. For some minerals the crystallinity of the starting basalt affected the amount which formed.Removal of Mg from seawater into solid alteration products occurred rapidly and was balanced largely by leaching of Ca from basalt. Net transfer of Na from seawater into solids occurred more slowly and was balanced mainly by leaching of additional Ca from basalt. Thus, reaction between seawater and basalt at low water/rock ratios can be considered to consist of two exchanges: Mg for Ca, and Na for Ca. 相似文献
110.
The theoretical disk brightness temperature spectra for Uranus are computed and compared with the observed microwave spectrum. It is shown that the emission observed at short centimeter wavelengths originates deep below the region where ammonia would ordinarily begin to condense. We demonstrate that this result is inconsistent with a wide range of atmospheric models in which the partial pressure of NH3 is given by the vapor-pressure equation in the upper atmosphere. It is estimated that the ammonia mixing ratio must be less than 10?6 in the 150 to 200°K temperature range. This is two orders of magnitude less than the expected mixing ratio based on solar abundances. The evidence for this depletion and a possible explanation are discussed. 相似文献