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11.
The northern Fossa Magna (NFM) basin is a Miocene rift system produced in the final stages of the opening of the Sea of Japan. It divides the major structure of Japan into two regions, with north-trending geological structures to the NE of the basin and EW trending structures to the west of the basin. The Itoigawa-Shizuoka Tectonic Line (ISTL) bounds the western part of the northern Fossa Magna and forms an active fault system that displays one of the largest slip rates (4–9 mm/year) in the Japanese islands. Deep seismic reflection and refraction/wide-angle reflection profiling were undertaken in 2002 across the northern part of ISTL in order to delineate structures in the crust, and the deep geometry of the active fault systems. The seismic images are interpreted based on the pattern of reflectors, the surface geology and velocities derived from refraction analysis. The 68-km-long seismic section suggests that the Miocene NFM basin was formed by an east dipping normal fault with a shallow flat segment to 6 km depth and a deeper ramp penetrating to 15 km depth. This low-angle normal fault originated as a comparatively shallow brittle/ductile detachment in a high thermal regime present in the Miocene. The NFM basin was filled by a thick (>6 km) accumulation of sediments. Shortening since the late Neogene is accommodated along NS to NE–SE trending thrust faults that previously accommodated extension and produce fault-related folds on their hanging wall. Based on our balanced geologic cross-section, the total amount of Miocene extension is ca. 42 km and the total amount of late Neogene to Quaternary shortening is ca. 23 km.  相似文献   
12.
Tetsuya  Waragai 《Island Arc》2005,14(4):368-377
Abstract   Calcretes can be observed on the surface of old moraines around Batura Glacier in the upper Hunza Valley, Karakoram Mountains, Pakistan. They develop as a calcareous crust cementing small gravels under boulders. In order to understand the genesis of the calcrete crust, a variety of methods were employed: (i) study of mineralogy and geochemistry of a calcrete crust precipitated on the lateral moraine using X-ray diffractometer and electron probe microanalysis; (ii) analysis of solute chemistry of surface water and ice bodies around the Batura Glacier; and (iii) accelerator mass spectrometry 14C dating of the crust itself. The results indicate that the calcrete crust has definite laminated layers composed of a fine-grain and compact calcite layer, and a mineral fragment layer. The chemical composition of the calcite layer is approximately 60% CaO and 1% MgO. The mineral fragment layer consists of rounded grain materials up to 0.2 mm in diameter. It shows a graded bedding structure with fine grains of quartz, albite and muscovite. Meanwhile, as the Paleozoic Pasu limestone is distributed around the terminal of Batura Glacier, Ca cations dissolve in the melt water of the glacier. Accordingly, the calcrete crust is precipitated by decreases in CO2 partial pressure from glacier ice and evaporation of the melt water, including high concentration of Ca2+ at ephemeral streams and small ponds stagnating between the moraine and glacial ice. On the basis of the AMS 14C age, the calcrete is considered to have formed approximately 8200 calibrated years bp under the Batura glacial stage.  相似文献   
13.
Fluid-undersaturated experiments were conducted to determine the phase relations in the simplified peridotite system MgO-SiO2-H2O (MSH) at 11.0-14.5 GPa and 800-1400 °C. Stability relations of dense hydrous magnesium silicates (DHMSs) under fluid-undersaturated conditions were experimentally examined. From the fluid-absent experimental results, we retrieved thermodynamic data for clinohumite, phase A, phase E, and hydrous wadsleyite, consistent with the published data set for dry mantle minerals. With this new data set, we have calculated phase equilibria in the MSH system including dehydration reactions. The dehydration reactions calculated with lower water activities of 0.68-0.60 match the fluid-present experiments of this study above 11.0 GPa and 1000 °C, indicating that considerable amounts of silicate component were dissolved into the fluid phase. The calculated phase equilibria illustrate the stability of the post-antigorite phase A-bearing assemblages. In the cold subducting slab peridotite, phase A + enstatite assemblage survives into the transition zone, whereas phase A + forsterite + enstatite assemblage forms hydrous wadsleyite at a much shallower depth of about 360-km. The slab is subducted with no dehydration reactions occurring when entering the transition zone. The phase equilibria also show the high temperature stability of phase E. Phase E is stable up to 1200 °C at 13.5 GPa, a plausible condition in the mantle of relatively low temperature, i.e., beneath subduction zones. Phase E is a possible water reservoir in the mantle as well as wadsleyite and ringwoodite.  相似文献   
14.
15.
We report Os isotope compositions of metal grains in two CBa chondrites (Bencubbin and Gujba) determined using a micromilling sampling coupled with thermal ionization mass spectrometry, together with the abundances of major and trace siderophile elements obtained by electron probe microanalysis and femtosecond laser ablation inductively coupled plasma–mass spectrometry. The CBa metal grains presented 187Os/188Os ratios akin to carbonaceous chondrites with limited variations (0.1257–0.1270). Most of the CBa metal grains were scattered along a 187Re-187Os reference isochron of IIIAB iron meteorites, indicating that the CBa metals experienced limited Re-Os fractionation at the time of their formation. The Re/Os ratios of sampling spots for the CBa metals, recast from the observed 187Os/188Os ratios, had a positive correlation with their Os/Ir ratios. In addition, the metal grains showed a positive correlation in a Pd/Fe versus Ni/Fe diagram. These correlations suggest that the CBa metal grains have formed via equilibrium condensation or evaporation from a gaseous reservoir at ~10−4 bar with enhanced metal abundances. Compared to the Bencubbin metals, the Gujba metals are characterized by having systematically lower Pd/Fe and Ni/Fe ratios that span subchondritic values. Such a difference was most likely induced by the compositionally heterogeneous impact plume from which the metals were condensed.  相似文献   
16.
Three surface sediments and two sediment cores were collected from the Gulf of Alaska, Bering Sea and Chukchi Sea, and analysed for persistent organochlorines (OCs). The geographical distributions of OCs showed different patterns according to their physicochemical properties. The concentrations of HCHs and HCB revealed rather uniform distribution, suggesting their more transportable nature in long-range atmospheric transport. On the other hand, DDTs and PCBs were predicted to be less transportable via the atmosphere due to the decreasing trends of residue levels in sediments from south to north. The OC profiles in the sediment core from the Gulf of Alaska which seemed to be preserved without turbation revealed the elevated residue levels from bottom to surface layers. This implies that the aerial inputs of OCs in the cold ocean are still continuing significantly. The accumulation rates of OCs into sediments were rather smaller than the atmospheric inputs, indicating that the residue levels in water bodies are unlikely to decrease rapidly in the near future.  相似文献   
17.
An interactive computer system has been developed to assist the mineral identification in ore microscopy. The reference file of the system consists of optical, mechanical, and chemical properties of about 130 ore minerals. The properties are name, chemical formula, color, bireflectance, anisotropism, internal reflection, reflectance at wavelengths of 470, 546, 589, and 650 nm, and polishing hardness and micro-indentation hardness. All the properties except reflectance and microindentation hardness are qualitative or semi-qualitative. Most of the properties are given as characters relative to the more common minerals. This implies that most of the identification processes advance on the basis of the comparison between a subject mineral and coexisting minerals. For this reason, the system asks a user at first to input already identified mineral names. This is quite different from the mineral identification procedures used in petrographic microscopy. To reduce the number of possible minerals, the system presents a series of questions to a user, and the user selects any of the prepared answers according to his observation. The user can also choose any desired question independently of the sequence. The user is expected to be able to recognize some common minerals, such as pyrite, chalcopyrite, galena, and hematite, without the assistance of the system.  相似文献   
18.
Oxygen isotope exchange rate between dissolved sulfate and water was experimentally determined at 100, 200 and 300°C. The isotope exchange rate is strongly dependent on temperature and pH of the solution. Combining the temperature and pH dependence of the reaction rate, the exchange reaction was estimated to be first-order with respect to sulfate. The logarithm of apparent rate constant of exchange reaction at a given temperature is a function of the pH calculated at the experimental temperatures. From the pH dependence of the apparent rate constant, it was deduced that the isotope exchange reaction between dissolved sulfate and water proceeds through collision between H2SO04 and H2O at low pH, and between HSO?4 and H2O at intermediate pH. The isotope exchange rate obtained indicates that oxygen isotope geothermometry utilizing the studied isotope exchange is suitable for temperature estimation of geothermal reservoirs. The extrapolated half-life of this reaction to oceanic temperature is about 109 years, implying that exchange between oceanic sulfate and water cannot control the oxygen isotope ratio of oceanic sulfates.  相似文献   
19.
The sulfide and sulfate contents and their δ34S values were determined in Quaternary volcanic rocks from the Japanese Islands Arc. The total sulfur contents are much lower (less than 40 ppm) and the δ34S values are higher (+4.4 ± 2.1) than those of ocean-floor basalts (800 ± 100 ppm and +0.8 ± 0.5, respectively; Moore and Fabbi, 1971; Sakaiet al., 1982). Lateral variations of both sulfur content and δ34S values were observed in the four volcanic belts in Japan. In the Northeast Japan belt, the sulfur content (30 ± 10 ppm) of the rocks in the inner zone (the Japan Sea side) is 3 to 5 times that in the outer zone (the Pacific side), although the δ34S values of the two zones are almost the same (+4.3 ± 1.0). The δ34S values for the two belts in West Japan are on the average 2%. higher than those of East Japan.This study suggests that the primary magmas that formed the island arc volcanic rocks are initially depleted in sulfur (<120 ppm) and enriched in 34S (δ34S: +5 ~ +7) compared to ocean-floor tholeiitic basalts which formed at mantle under oceanic region. This indicates that the upper-mantle is heterogeneous in sulfur content and isotope composition.  相似文献   
20.
Analysis of physical properties in long sediment cores (BDP96) from Academician Ridge in Lake Baikal indicates that major climato-limnological changes during the past 3.5 Myr occurred at about 2.5–2.8, 1.7–1.9, and 0.9–1.2 Ma, which were close to times of major geomagnetic polarity reversals (Matuyama/Gauss, Olduvai, Jaramillo + Matuyama/Brunhes). The principal climato-limnological oscillation has a long-term period of nearly 1,000 kyr, which corresponds to the periodicity of fluctuation in solar insolation. It also seems to be related to geomagnetic field intensity. Other long-term period of 400 kyr corresponds to Milankovitch parameters of eccentricity. These results suggest that changes in solar insolation were closely related to long-term environmental variations in the deep continental interior.  相似文献   
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