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61.
62.
Seismicity located by using the most recent data obtained from the high-gain seismograph network of Tohoku University shows that the deep seismic zone beneath northeastern Honshu, Japan, is composed of two thin planes which are parallel to each other and are 30–40 km apart. Focal mechanisms derived from the earthquakes in the upper plane are reverse-faulting, or, some of them, down-dip compression. As a contrast, those in the lower plane are down-dip extension. The location of the upper boundary of the descending lithospheric slab, inferred from the arrival-time difference between ScS and ScSp waves and from the travel-time anomaly of intermediate-depth earthquakes observed at the small-scale seismic array, coincides exactly with the upper plane of the double-planed deep seismic zone. Anelasticity (1/Q) structure of the upper mantle consists of three distinct zones: a high-Q (Qs− 1500) inclined lithospheric slab, an intennediate-Q (Qs−350) land-side mantle between the Pacific coast and the volcanic front, and a low-Q (Qs − 100) land-side mantle between the volcanic front and the coast of the Japan Sea.The evidence obtained here provides valuable information as to the definition of the type of mechanism producing the plate motion beneath island arcs.  相似文献   
63.
Labradorite was altered artificially by HC1 solution ranging from M = 1 to M = 0.003 at 245 and 230°C. The products of alteration were examined by X-ray diffraction, electron microscopy, electron diffraction, infrared spectroscopy and the electron microprobe and the solution was analyzed chemically.Amorphous silica only was formed in solutions with MHCl = 1 and MHCl = 0.3. In a solution with MHCl = 0.2, amorphous silica was initially formed, later dissolved and replaced by kaolinite. A mixture of microcrystalline boehmite and amorphous aluminosilicate was formed, altering to kaolinite in solutions with MHCl = 0.1 and 0.3. Small amounts of kaolinite were initially formed but the alteration soon stopped in solution with MHCl = 0.003. Relationships between the alteration processes and pH of the solutions can be roughly explained by using solubility diagrams assuming the congruent dissolution of labradorite and precipitation of the products in partial equilibrium. However, these assumptions are not valid with strongly acid solutions.The rate of dissolution of labradorite is controlled not only by its surface area, but also by the diffusion of matter through the layer of alteration products.  相似文献   
64.
An unusual association of chromite and hornblende was found in the spessartites of andesite composition, occurring as a dike swarm associated with a Cretaceous granite batholith. The spessartites are largely porphyritic with phenocrysts of either hornblende or augite. One dike, comprising a finegrained spessartite, exhibits distinct chilled selvages of aphanitic facies. The chromites in the fine-grained and augite-spessartites are significantly higher in Cr/ (Cr+Al) than those occurring rarely as inclusions in the phenocrystic hornblendes in the hornblende spessartite, although both are similar in Mg/ (Mg+Fe), Fe2O3, and TiO2. The phenocrystic hornblendes are titaniferous pargasite with high Mg/ (Mg+Fe), and differ in their higher octahedral Al from the groundmass hornblendes including those in the fine-grained spessartite. The crystallization sequence in the phenocrystic hornblende-bearing spessartites is Al-rich chromite, phenocrystic hornblende, and plagioclase without pyroxene, suggesting a high water content in the magma and the start of the crystallization at relatively high pressures. The finegrained spessartite from which the porphyritic spessartites have been derived by fractionation of dominant mafic minerals, has the high Mg-value and Cr content equivalent to those in primitive, undifferentiated basalts, although still andesitic in SiO2 content. Chemically similar magnesian andesites, although uncommon, found in some orogenic calc-alkalic suites may represent a magma composition in equilibrium with mantle peridotite under the condition of high water pressures.  相似文献   
65.
The accurate measurement of thermal expansion in spinel MgAl2O4 over a temperature range between 30° C and 900° C has revealed an anomalous behaviour indicating a possible presence of a second order phase transition at 660° C.  相似文献   
66.
The relationship between island-induced cyclonic eddies and chlorophyll a (chl-a) was investigated using field data and satellite images in the eastern channel of the Tsushima Straits. The maximum chl-a concentration around the leeward eddy of the Tsushima Islands was two or three times greater than that of outside the eddy. Two different mechanisms of chl-a enhancement associated with island-induced cyclonic eddies were found in the post-bloom periods. In summer, when nutrients were depleted in the surface layer, eddy pumping increased the nutrient supply in the euphotic zone, resulting in enhanced chl-a around the shallow thermocline near the eddy core. In late autumn, when the mixed layer deepened over the euphotic zone, the mixed layer depth became shallow due to the doming effect of the cyclonic eddy, therefore, the improved irradiance condition led to an increase in the chl-a concentration in the surface mixed layer. Nighttime satellite visible images showed a number of fishing vessels in the lee region of the Tsushima Islands, implying that the enhanced phytoplankton biomass may have resulted in good feeding conditions for fishes and squids in the Tsushima Straits.  相似文献   
67.
68.
Besshi-type Cu deposits are strata-bound volcanogenic massive sulfide deposits usually associated with mafic volcanic rocks or their metamorphic equivalents. Although there are numerous Besshi-type deposits in the Sanbagawa metamorphic belt, Japan, their tectonic settings and depositional environments remain controversial because of a lack of depositional age constraints. We report Re-Os data for the Iimori deposit, one of the largest Besshi-type deposits in western Kii Peninsula, in order to examine the robustness of the Re-Os isotope system for dating sulfide minerals in the high-P/T metamorphic belt and to elucidate the primary depositional environment of the Iimori sulfide ores. An 11-point Re-Os isochron plot yields an age of 156.8 ± 3.6 Ma. As this Re-Os isochron age is significantly older than the timing of the Sanbagawa peak metamorphism (110-120 or ∼90 Ma) and a well-defined isochron was obtained, the Re-Os age determined here is most likely the primary depositional age. Despite high-grade metamorphism at up to 520 ± 25 °C and 8-9.5 kbar, the Re-Os isotope system of the Iimori sulfides was not disturbed. Hence, we consider that the whole-rock Re-Os closure temperature for the Iimori sulfide ores was probably higher than 500 °C. As the accretion age of the Sanbagawa metamorphic belt is considered to be 120-130 or 65-90 Ma on the basis of radiolarian and radiometric ages, we estimated the time from the Iimori sulfide deposition on the paleo-seafloor to its accretion at the convergent plate boundary to be greater than 25 Myr. Consequently, the depositional environment of the Iimori sulfide ores was not in the marginal sea, but was truly pelagic.  相似文献   
69.
We performed a comprehensive metaproteomic analysis of the dissolved organic matter (DOM) in Japanese coastal waters using liquid chromatography–tandem mass spectrometry and demonstrated that these proteomes were characterized by proteins with various functions, including metabolic enzymes, membranes, and photosynthetic proteins. The protein sources included cyanobacteria, heterotrophic bacteria, and eukaryotic phytoplankton. Most of the components were similar among samples and also similar to pelagic components. We also observed differences in the compositions of the microbial communities of origin among the different dissolved protein samples and differences in the relative abundance of specific dissolved protein types (e.g., cytoskeletal proteins), possibly indicating potential dynamics in the coastal DOM pool.  相似文献   
70.
We measured dissolved isoprene (2-methyl-1,3-butadiene; C5H8) concentrations in a broad area of the southern Indian Ocean and in the Indian sector of the Southern Ocean from 35°S to 64°S and from 37°E to 111°E during austral summer 2010–2011. Isoprene concentrations were continuously measured by use of a proton-transfer-reaction mass spectrometer combined with a bubbling-type equilibrator. Concentrations of isoprene and its emission flux throughout the study period ranged from 0.2 to 395 pmol L?1 and from 181 to 313 nmol m?2 day?1, respectively, the averages being generally higher than those of previous studies. Although we found a significant linear positive relationship between isoprene and chlorophyll-a concentrations (r 2 = 0.37, n = 36, P < 0.001), the correlation coefficient was lower than previously reported. In contrast, in the high-latitude area (>53°S) we identified a significant negative correlation (r 2 = 0.59, n = 1263, P < 0.001) between isoprene and the temperature-normalized partial pressure of carbon dioxide (n-pCO2), used as an indicator of net community production in this study. This suggests that residence times and factors controlling variations in isoprene and n-pCO2 are similar within a physically stable water column.  相似文献   
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