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801.
802.
V. Piscopo M. Barbieri V. Monetti G. Pagano S. Pistoni E. Ruggi D. Stanzione 《Hydrogeology Journal》2006,14(8):1508-1521
A conceptual hydrogeological model of the Viterbo thermal area (central Italy) has been developed. Though numerous studies have been conducted on its geological, geochemical and geothermal features, there is no generalized picture defining the origin and yield of the hydrothermal system. These latter aspects have therefore become the objectives of this research, which is based on new hydrogeological and geochemical investigations. The geological setting results in the coexistence of overlapped interacting aquifers. The shallow volcanic aquifer, characterized by fresh waters, is fed from the area around the Cimini Mountains and is limited at its base by the semiconfining marly-calcareous-arenaceous complex and low-permeability clays. To the west of Viterbo, vertical upflows of thermal waters of the sulphate-chloride-alkaline-earth type with higher gas contents, are due to the locally uplifted carbonate reservoir, the reduced thickness of the semiconfining layer and the high local geothermal gradient. The hot waters (30–60°C) are the result of deep circulation within the carbonate rocks (0.5–1.8 km) and have the same recharge area as the volcanic aquifer. The upward flow in the Viterbo thermal area is at least 0.1 m3/s. This flow feeds springs and deep wells, also recharging the volcanic aquifer from below. 相似文献
803.
V. I. Vinogradov G. A. Belenitskaya M. I. Bujakaite V. N. Kuleshov M. A. Minaeva B. G. Pokrovskii 《Lithology and Mineral Resources》2006,41(3):271-279
In previous communications based on the study of sulfur and strontium, we showed that Lower Cambrian rocks of the Irkutsk Amphitheater underwent a significant epigenetic transformation. All postsedimentary alterations of rocks are related to the influence of water solutions that provoke the direct (physical) dissolution of material and its chemical transformation. In particular, an appreciable portion of anhydrites disappeared from the section due to reduction. Probably, these processes took place several times in the past and they are continuing at present. A similar conclusion was deduced from the strontium isotopic composition of carbonate rocks. Their strontium isotopic composition is usually shifted relative to the primary composition, although the prevalence of sulfate and carbonate rocks in the section promotes the stability of strontium isotopic composition with respect to secondary alterations. The carbon isotope system is even more stable due to the abundance of carbonate rocks in the section. This circumstance is probably responsible for the incapacity of isotope data to serve as obvious evidence of the epigenetic transformation of carbonates. The major elements of the evolution of carbon isotope signature could be retained since the sedimentation stage. 相似文献
804.
805.
C. E. Runge A. Kubo B. Kiefer Y. Meng V. B. Prakapenka G. Shen R. J. Cava T. S. Duffy 《Physics and Chemistry of Minerals》2006,33(10):699-709
The equation of state of MgGeO3 perovskite was determined between 25 and 66 GPa using synchrotron X-ray diffraction with the laser-heated diamond anvil cell. The data were fit to a third-order Birch–Murnaghan equation of state and yielded a zero-pressure volume (V 0) of 182.2 ± 0.3 Å3 and bulk modulus (K 0) of 229 ± 3 GPa, with the pressure derivative (K′0 = (?K 0/?P) T ) fixed at 3.7. Differential stresses were evaluated using lattice strain theory and found to be typically less than about 1.5 GPa. Theoretical calculations were also carried out using density functional theory from 0 to 205 GPa. The equation of state parameters from theory (V 0 = 180.2 Å3, K 0 = 221.3 GPa, and K′0 = 3.90) are in agreement with experiment, although theoretically calculated volumes are systematically lower than experiment. The properties of the perovskite phase were compared to MgGeO3 post-perovskite phase near the observed phase transition pressure (~65 GPa). Across the transition, the density increased by 2.0(0.7)%. This is in excellent agreement with the theoretically determined density change of 1.9%; however both values are larger than those for the (Mg,Fe)SiO3 phase transition. The bulk sound velocity change across the transition is small and is likely to be negative [?0.5(1.6)% from experiment and ?1.2% from theory]. These results are similar to previous findings for the (Mg,Fe)SiO3 system. A linearized Birch–Murnaghan equation of state fit to each axis yielded zero-pressure compressibilities of 0.0022, 0.0009, and 0.0016 GPa?1 for the a, b, and c axis, respectively. Magnesium germanate appears to be a good analog system for studying the properties of the perovskite and post-perovskite phases in silicates. 相似文献
806.
807.
A comparative geochemical study of rare-metal granitoids with various fluorine-bearing minerals (fluorite, topaz, and cryolite)
was carried out. It was shown that these rocks correspond to both plumasitic and agpaitic geochemical types. The fluorite-,
topaz-, and cryolite-bearing granites of these geochemical types are distinctly different in geochemical parameters and the
character of magmatic evolution. These differences are related to the composition of initial magmas and their sources. Rare-metal
granitoids with fluorine-bearing minerals compose small massifs, stocks, and dike swarms. Their formation is independent of
the composition and age of the country rocks or geologic structures where they occur.
Original Russian Text ? V.S. Antipin, E.A. Savina, M.A. Mitichkin, 2006, published in Geokhimiya, 2006, No. 10, pp. 1040–1052. 相似文献
808.
A. V. Maslov V. N. Podkovyrov Yu. L. Ronkin M. T. Krupenin E. Z. Gareev V. M. Gorozhanin 《Stratigraphy and Geological Correlation》2006,14(2):126-149
In the mid-1980s, it was concluded based on geochemical study that Th, Sc, La concentrations and ratios Th/Sc, La/Sc and Eu/Eu* did not wary significantly in the post-Archean time. It was impossible to judge about compositional variations of upper crust during the Riphean and Vendian, because data of that time characterized a limited number of samples from the post-Archean basins of Australia, New Zealand, and Antarctic. Considered in this work are variations of Eu/Eu*, LREE/HREE, Th/Sc, and La/Sc ratios in Upper Precambrian fine-grained siliciclastic rock of the Southern Urals western flank (Bashkirian meganticlinorium) and Uchur-Maya region (Uchur-Maya plate and Yudoma-Maya belt). As is established, only the Eu anomaly in the studied siliciclastic rocks is practically identical to this parameter of the average post-Archean shale. Three other parameters plot on the Riphean-Vendian variation curves with positive and negative excursions of diverse magnitude, which do not coincide always in time. It is assumed that these excursions likely mark stages of local geodynamic activity, destruction of pre-Riphean cratons, and progressing recycling of sedimentary material during the Riphean. 相似文献
809.
A. B. Kuznetsov M. A. Semikhatov A. V. Maslov I. M. Gorokhov E. M. Prasolov M. T. Krupenin I. V. Kislova 《Stratigraphy and Geological Correlation》2006,14(6):602-628
New data on Sr-and C-isotopic systematics of carbonate rocks from the Upper Riphean stratotype (Karatau Group of the southern Urals) are obtained for several southwestern sections of the Bashkirian meganticlinorium, which have not been studied before. The results obtained supplement the Sr-and C-isotopic information for the group upper horizons thus detailing chemostratigraphic characterization of the entire succession. Limestone and dolostone samples used to analyze the Sr isotope composition satisfy strict geochemical criteria of the isotopic system retentivity and have been subjected to preliminary treatment in ammonium acetate to remove secondary carbonate phases. Data on 255 samples of carbonate rocks (171 studied for the first time) show that δ13C value varies in the Karatau Group succession from ?2.8 to +5.9 ‰ V-PDB with several in-phase excursions from the general trend in all the sections studied in the area 90 × 130 km. The δ13C variation trend demarcates several levels in the carbonate succession of the Karatau Group suitable for objectives of regional stratigraphy and for C-isotope chemostratigraphic subdivision of the Upper Riphean. The results of Sr isotopic analysis of 121 samples (51 unstudied before) from the Karatau Group imply that rocks in its lower part (the Katav Formation and basal horizon of the Inzer Formation) experienced considerable secondary alterations, while limestones and dolostones of the overlying interval of the group are frequently unaltered. In the “best” samples satisfying geochemical criteria of the isotopic system retentivity, the 87Sr/86Sr initial ratio increases from 0.70521–0.70532 in the lower Inzer deposits to 0.70611 in the upper Min’yar carbonates, decreasing to <0.70600 near the top of the latter. Above the regional hiatus separating the Min’yar and Uk formation, this ratio grows from 0.70533 to 0.70605–0.70609 in the limestone succession of the last formation. 相似文献
810.