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61.
Christine Destrigneville Jacques Schott Yves Caristan Pierre Agrinier 《Earth and Planetary Science Letters》1991,104(2-4)
Evidence for a deuteric alteration process induced by a magmatic fluid has been found in the feeder zone of the Mururoa volcano (French Polynesia). Within the dikes, where basaltic glass does not show any evidence of pervasive alteration, vesicles are filled with dioctahedral smectites and calcite, while olivine phenocrysts are replaced by dioctahedral smectites, ankerite and calcite.The 13C signature of carbonates, the carbon and H2O content of the whole rocks and their impoverishment in deuterium are compatible with the presence of magmatic CO2 during the crystallization of intruding lavas and exclude contamination by seawater. Mass balance calculations on selected thin sections photographs of partly filled up vesicles and replaced olivine crystals, constrain, assuming a closed system interaction, the chemical composition of the initial fluid and the respective amounts of the initial solid phases involved in the alteration process. Thermodynamic modelings using the EQ3/6 software package correctly predict the mineralogic, chemical and isotopic exchanges accompanying alteration, thus validating the closed system assumption. The model which allows prediction of the influence of CO2 on the alteration products, shows that, above a 0.25 CO2 mole fraction in the initial fluid, the alteration is entirely controlled by the chemical composition of the initial solid phases. The presence of CO2 implies the precipitation of dioctahedral smectites and carbonates instead of the magnesian smectites commonly observed in CO2-free systems.The Mururoa feeder zone shows alteration features typical of a closed system interaction between the basaltic rock and a magmatic fluid in which seawater did not take part. 相似文献
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Emmanuelle Montarges-Pelletier Laurent Jeanneau Pierre Faure Isabelle Bihannic Odile Barres Bruno S. Lartiges 《Environmental Geology》2007,53(1):85-102
The Moselle river flows in the north-east of France, from Vosges Mountains to neighboring countries Luxembourg and Germany.
One of its tributaries, the Fensch river, drains a highly industrialized watershed, strongly impacted by mining, smelting
and surfacing activities. The objective of this work, part of a general research program on Moselle watershed (Zone Atelier
Moselle) was to assess the impact of the polluted Fensch river on the global quality of the Moselle river. For that purpose,
water, sediments and suspended particulate matter were sampled in both rivers, upstream and downstream the junction. Four
main sampling campaigns were carried out, in winter during a flood event and in spring at low water level. On a first step,
mineralogical analyses (XRD and FTIR) and chemical analyses (ICP-MS, ICP-AES), were performed on sediments, suspended particulate
matters and filtered waters. Major and trace elements concentrations were obtained on two different granulometric fractions
(0–2 mm and 0–50 μm) revealing the enrichment in heavy metals of fine particles. From one collecting campaign to another,
seasonal variations could be evidenced on suspended matter composition even though major minerals (calcite, quartz and kaolinite)
were always present. Furthermore, spatial variations were evidenced for Fensch and Moselle downstream sediments. Thus, very
fine-grained sediments, poorly crystallized, displaying at the same time higher metal concentrations and higher organic matter
content than in Fensch river material, were collected downstream, in a low hydrodynamic conditions zone, assumed as a preferential
sedimentary zone or even as a placer. Strong correlations could be revealed between iron content and contaminant concentrations,
confirming the origin of polluted material. 相似文献
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Fluid composition and evolution in coesite-bearing rocks (Dora-Maira massif,Western Alps): implications for element recycling during subduction 总被引:10,自引:0,他引:10
Pascal Philippot Pierre Chevallier Christian Chopin Jean Dubessy 《Contributions to Mineralogy and Petrology》1995,121(1):29-44
Fluid inclusions and F, Cl concentration of hydrous minerals were analysed in the coesite-pyrope quartzite, the interlayered jadeite quartzite and their country-rock gneiss from the Dora-Maira massif using a combination of microthermometry, Raman spectrometry, synchrotron X-ray microfiuorescence and electron microprobe analysis. Three populations of fluid inclusions were recognized texturally and can be related to distinct metamorphic stages. A low-salinity aqueous fluid occurs in the retrogressed country gneiss and as late secondary inclusions in jadeite quartzite and chloritized pyrope. An earlier secondary population is found in matrix quartz of the jadeite- and pyro-pe-quartzites. This population can be related to the early decompression and so to incipient breakdown of garnet into phlogopite-bearing assemblages. The inclusion fluid is highly saline (up to 84 wt% equivalent NaCl) and contains Na, Ca, Fe, Cu and Zn as major cations. In pyrope quartzite, additional K was found in these brines, which locally coexist with CO2-rich inclusions. The oldest fluid inclusions are preserved in kyanite grains included in fresh pyrope and in pyrope itself. In pyrope, all inclusions have decrepitated and contain magnesite, an Mg-phosphate, sheet-silicate(s), a chloride and an opaque phase, with no fluid preser ved. In contrast, the kyanite inclusions in pyrope preserve primary H2O-CO2 low-salinity fluid inclusions, probably owing to the low compressibility of the kyanite inclusions and host garnet. In spite of in-situ re-equilibration, these inclusions can be interpreted as relics of the dehydration fluid that attended pyrope growth. These correlations between textural and chemical fluid inclusion data and metamorphic stages are consistent with the fluid composition calculated from the halogen content of different generations of phlogopite and biotite. The preservation of different fluid compositions, both in time and space, is evidence for local control and possibly origin of the fluids, in agreement with isotopic data. These results, in particular the absence of CO2 in the jadeite quartzite, are best interpreted in terms of a fluid-melt system evolution. With increasing metamorphism, partitioning of H2O, Na, Ca, Fe and heavy metals into melt (jadeite quartzite) and Mg, Na/K, F, CO2 and P(?) into a residual aqueous fluid can account for depletion in Na, Ca and Fe of the pyrope quartzite. During the retrograde path, a H 2 O rose as melt crystallized, generating the two populations of hypersaline and water-rich fluids that were highly reactive to pyrope. The process of fluid-melt interaction envisioned here coupled with models of melt extraction in subduction zones provides an attractive opportunity for the instantaneous ( < 1 Ma) and selective transport of elements between a downgoing slab and the overlying mantle wedge. 相似文献
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