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1.
The potential of heterotrophs to degrade aromatic hydrocarbons derived from oil in water and sediments in the northern North Sea around the Brent, Beryl, Forties and Murchison oilfields and at a number of stations, from the Forties field to the Firth of Forth, was estimated using 1-14C naphthalene and 7, 10-14C benzo(a)pyrene. The degradation of uniformly labelled 14C mixed 1-amino acids was used as a measure of total heterotrophic activity. Results showed that microorganisms have the potential to degrade the smaller aromatic hydrocarbon molecules rapidly in the water column and in surface sediments. Close to the Beryl platform, where diesel-washed drill cuttings have been continuously dumped, the rate of input of hydrocarbons to the sediment has exceeded the rate of degradation. Mineralization of benzo(a)pyrene, estimated in the sediments only, was minimal. Close to production platforms the biodegradation rate of mixed 1-amino acids showed no increase comparable with that found for naphthalene, suggesting that existing microbial populations had not increased but adapted to degrade oil in water and sediments.  相似文献   
2.
Distribution of Ferric Iron in some Upper-Mantle Assemblages   总被引:16,自引:5,他引:11  
The distribution of ferric iron among the phases of upper-mantlerocks, as a function of pressure (P), temperature (T) and bulkcomposition, has been studied using 57Fe Mssbauer spectroscopyto determine the Fe3+/Fe ratios of mineral separates from 35peridotite and pyroxenite samples. The whole-rock Fe3+ complementof a peridotite is typically shared approximately evenly amongthe major anhydrous phases (spinel and/or garnet, orthopyroxeneand clinopyroxene), with the important exception of olivine,which contains negligible Fe3+. Whole-rock Fe3+ contents areindependent of the T and P of equilibration of the rock, butshow a well-defined simple inverse correlation with the degreeof depletion in a basaltic component. Fe3+ in spinel and inboth pyroxenes from the spinel Iherzolite facies shows a positivecorrelation with temperature, presumably owing to the decreasein the modal abundance of spinel. In garnet peridotites, theFe3+ in garnet increases markedly with increasing T and P, whereasthat in clinopyroxene remains approximately constant. The complexnature of the partitioning of Fe3+ between mantle phases resultsin complicated patterns of the activities of the Fe3+ -bearingcomponents, and thus in calculated equilibrium fO2, which showlittle correlation with whole-rock Fe3+ or degree of depletion.Whether Fe3+ is taken into account or ignored in calculatingmineral formulae for geothermobarometry can have major effectson the resulting calculated T and P. For Fe-Mg exchange geothermometers,large errors must occur when applied to samples more oxidizedor reduced than the experimental calibrations, whose fO2 conditionsare largely unknown. Two-pyroxene thermometry is more immuneto this problem, and probably provides the most reliable P—Testimates. Accordingly, the convergence of P—T valuesderived for a given garnet peridotite assemblage may not necessarilybe indicative of mineral equilibrium. The prospects for thecalculation of accurate Fe3+ contents from electron microprobeanalyses by assuming stoichiometry are good for spinel, uncertainfor garnet, and distinctly poor for pyroxenes. KEY WORDS: mantle; oxidation; partitioning; peridotite; thermobarometry *Corresponding author. Present address: School of Earth and Ocean Sciences, University of Victoria, P.O. Box 1700, Victoria, B.C., V8W 2Y2, Canada  相似文献   
3.
The solubility of sulfur as S2– has been experimentallydetermined for 19 silicate melt compositions in the system CaO–MgO–Al2O3–SiO2(CMAS)± TiO2 ± FeO, at 1400°C and 1 bar, using CO–CO2–SO2gas mixtures to vary oxygen fugacity (fO2) and sulfur fugacity(fS2). For all compositions, the S solubility is confirmed tobe proportional to (fS2/fO2)1/2, allowing the definition ofthe sulfide capacity (CS) of a silicate melt as CS = [S](fO2/fS2)1/2.Additional experiments covering over 150 melt compositions,including some with Na and K, were then used to determine CSas a function of melt composition at 1400°C. The resultswere fitted to the equation  相似文献   
4.
5.
At Kabbaldurga, infiltration of carbonic fluids along a systemof ductile shears and foliation planes has led to partial transformationof Archaean grey biotite–hornblende gneiss to coarse-grainedmassive charnockite at about 2.5 b.y. ago. The dehydration ofthe gneiss assemblage was induced by a marked metasomatic changeof the reacting system from granodioritic to granitic, and obviouslytook place under conditions of an open system at 700–750?C and 5–7 kb. Extensive replacement of plagioclase (An16–30)by K-feldspar through Na, Ca–K exchange reactions withthe ascending carbonic fluids led to strong enrichment in K,Rb, Ba, and SiO2, and to a depletion in Ca. Progressive dissolutionof hornblende, biotite, magnetite, and the accessory mineralsapatite and zircon resulted in a marked depletion in Fe, Mg,Ti, Zn, V, P, and Zr. Most important is the recognition of REEmobility: with advancing charnockitization, the moderately fractionatedREE distribution patterns of the grey gneisses (LaN270; LaN/YbN= 5–20; EuN27; Eu/Eu* = 0.6–0.3) give way to stronglyfractionated REE patterns with a positive Eu-anomaly (LaN200;LaN/YbN = 20–80; EuN22; Eu/Eu* = 0.6–1.8). The systematicdepletion especially in the HREE is due to the progressive dissolutionof zircon, apatite (and monazite), which strongly concentratethe REE. Stable isotope data (18O of 6.9–8.0 per mille for gneissesand charnockites; 13C of –8.5 and –6.5 per millefor late carbonate) indicate a magmatogenic source for the carbonicfluids. In contrast to the currently favoured derivation ofcarbonic fluids by decarbonation of the upper mantle or degassingof underplated basaltic intrusions, it is discussed here thatabundant fluid inclusions in lower crustal charnockites providedan extensive reservoir of ‘fossil’ carbonic fluids.Shear deformation has tapped this reservoir and generated thechannel-ways for fluid ascent. Charnockitization of the Kabbaldurgatypethus appears to be a metasomatic process which is tectonicallycontrolled and restricted to the crustal level of the amphiboliteto granulite transition.  相似文献   
6.
Hydrogen solubility and hydroxyl substitution mechanism in olivineat upper-mantle conditions are not only a function of pressure,temperature, water fugacity and hydrogen fugacity, but are alsoinfluenced by silica activity. Olivine synthesized in equilibriumwith magnesiowüstite displays hydroxyl stretching bandsin the wavenumber range from 3640 to 3430 cm–1. In contrast,olivine in equilibrium with orthopyroxene shows absorption bandsin a narrower wavenumber range from 3380 to 3285 cm–1.The two fundamentally different spectra are assigned to hydroxylin tetrahedral and octahedral sublattices, respectively. Olivinein equilibrium with orthopyroxene is also less capable of incorporatinghydroxyl, relative to olivines in equilibrium with magnesiowüstite,by about a factor of ten. A comparison of spectra obtained aspart of this study with hydroxyl spectra of natural mantle olivinesshows that the latter display hydroxyl stretching patterns reminiscentof equilibrium with magnesiowüstite, although undoubtedlyolivine in the Earth’s mantle coexists with orthopyroxene.This may be attributed to a metasomatic overprint by a low-silicafluid and/or melt that was in reaction relationship with orthopyroxene.A likely metasomatic agent is a carbonatitic melt. When carbonatiticmelts decompose to oxides and CO2, they may temporarily imposea low-aSiO2 environment inherited by the olivine structure.If this suggestion proves true, Fourier transform IR spectroscopymay be used to fingerprint metasomatic episodes in the lithosphericmantle. KEY WORDS: FTIR spectrometry; olivine; mantle; metasomatism; water  相似文献   
7.
Analysis of a Miocene-Pleistocene ice-rafted debris (IRD) record from the western Irminger Basin provides evidence for the initiation and long-term behavior of the SE portion of the Greenland Ice Sheet. In the late Miocene (~7.3 Ma), IRD supply to Ocean Drilling Program site 918 increased significantly indicating that glaciers large enough to reach sea level were present in SE Greenland long before the onset of widespread Northern Hemisphere glaciation. IRD accumulated at this site throughout the Pliocene and Pleistocene, supporting the hypothesis that SE Greenland was a key nucleation area for the formation of the Greenland Ice Sheet. Since glacial onset, the western Irminger Basin IRD record is characterized by a succession of episodes with high IRD mass accumulation rates (MARs). The site 918 IRD record indicates that greatest iceberg production in SE Greenland occurred during major climatic transitions (e.g. widespread Northern Hemisphere glacial expansion at 2.7 Ma and the mid-Pleistocene climate shift at 0.9 Ma), and that SE Greenland sometimes also led the northern North Atlantic region in glacial response to climatic forcing (e.g. glacial intensification at ~4.8 and, along with NE Greenland, at ~3.5 Ma).  相似文献   
8.
This report investigates the suggestion that the pattern of plasma convection in the polar cleft region is directly determined by the interplanetary electric field (IEF). Owing to the geometrical properties of the magnetosphere, the East-West component of the IEF will drive field-aligned currents which connect to the ionosphere at points lying on either side of noon, while currents associated with the North-South component of the IEF will connect the two polar caps as sheet currents centered at noon. The effects of the hypothesized IEF driven cleft current systems on polar cap ionospheric plasma convection are investigated through a series of numerical simulations. The simulations demonstrate that this simple electrodynamic model can account for the narrow “throats” of strong dayside antisunward convection observed during periods of southward interplanetary magnetic field (IMF) as well as the sunward convection observed during periods of strongly northward IMF. Thedawn-dusk shift of polar cap convection which is related to the By component of the IMF is also accounted for by the model.  相似文献   
9.
A re-evaluation of the threat status of New Zealand's marine invertebrates was undertaken in 2009, following earlier review of New Zealand's Threat Classification System and subsequent refinement of the national criteria for classifying threat of extinction to New Zealand's flora and fauna. Sufficient information was available to enable 295 marine invertebrate taxa to be fully evaluated and assigned to a national threat category. The 10 taxa at most risk of extinction (‘nationally critical’) were the giant seep clam Calyptogena sp., the primitive acorn barnacle Chionelasmus crosnieri, O'Shea's vent barnacle Volcanolepas osheai, the stalked barnacle Ibla idiotica, the four-blotched umbrella octopus Cirroctopus hochbergi, the roughy umbrella octopus Opisthoteuthis chathamensis, the giant squid Idioteuthis cordiformis, the large-egged polychaete Boccardiella magniovata and two gravel maggots, Smeagol climoi and Smeagol manneringi. The key threatening processes identified for marine invertebrates were fishing and land-use associated impacts such as sedimentation. We identified no taxa that had improved in threat status as a result of past or ongoing conservation management action, nor any taxa that had worsened in threat status because of known changes in their distribution, abundance or rate of population decline. We evaluated a small fraction of New Zealand's marine invertebrate fauna for their threat status. Many taxa remain ‘data deficient’ or unlisted. In addition to the most threatened taxa, we recommend these taxa and their habitats as priorities for further survey and monitoring.  相似文献   
10.
Hitherto Jupiter's spectrum at short millimeter wavelenghts showed a clear discrepancy with model calculations (e.g., G.L. Berge and S. Gulkis, 1976, In Jupiter (T. Gehrels, Ed.), pp. 621–692. Univ. of Arizona Press, Tucson). A similar although less pronounced, discrepancy appears to exist for Uranus and Neptune. One explanation of this discrepancy is that additional absorbers not included in the model calculations are present in the atmosphere. It was suggested that uncertainties in the absorption coefficient of ammonia, especially at millimeter wavelengths, may be responsible for at least part of the discrepancy. A comparison of various model atmosphere calculations with data for all four giant planets is shown. The absorption profile of ammonia at centimeter wavelengths was assumed to be rightly represented by a Ben Reuven line profile, which enabled the derivation of information on the vertical distribution of ammonia in these planets' atmospheres. It appeared that ammonia must be depleted in the upper atmospheres of all four planets by a factor of 4–5 with respect to the solar abundance for Jupiter (and Saturn) and by a factor of 100–200 for Uranus and Neptune. At deeper layers the optical depth is larger, due either to a larger abundance of ammonia or to absorption by the presence of water. Given the vertical ammonia distribution in the atmospheres as derived from the centimeter data, a best fit to the millimeter spectra of all four planets was found by changing the high frequency tail of the ammonium lineshape profile. This, we feel, is legitimate since the profile at millimeter wavelenghts is not or is only poorly known due to the absence of laboratory spectra for ammonia as a trace constituent in an otherwise hydrogen gas. It was found that a line profile which at millimeter wavelenghts more closely resembles a Van Vleck-Weisskopf lineshape than the usually adopted Ben Reuven profile gives a rather satisfactory fit to the data of all four gaseous planets.  相似文献   
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