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131.
云南兰坪-思茅盆地中一新生代砂页岩中赋存有许多脉状铜矿床。本文对盆地内从北至南三个典型脉状铜矿床(金满、水泄和白龙厂)进行了详细的铅、硫同位素研究,探讨了该类型矿床的成矿物质来源。分析表明。该类型矿床的铅同位素组成总体变化较小,且均位于上地壳铅演化线附近,说明成矿流体中铅具有稳定的上地壳来源。各矿床由于赋矿层位不同,矿石铅同位素组成表现出一定差异,如由兰坪盆地侏罗纪地层中的金满矿床到思茅盆地二叠纪地层中的白龙厂矿床,铅同位素比值(^207Pb/^204Pb)呈增高趋势,这表明这类矿床的铅主要来源于围岩地层,且地层越老,提供的铅就相对富含放射成因铅。矿床中脉石矿物重晶石、铁白云石等的锶同位素组成也表明,金满矿床成矿流体的^87Sr/^86Sr比值较高(0.70874—0.71232),而白龙厂矿床的^87Sr/^86Sr比值较低(0.70829—0.70938),接近于围岩灰岩的值(0.70755)。硫同位素研究表明,金满矿床中硫化物的δ^34S值变化最大,为-20.5‰- 7.0‰。水泄矿床中硫化物的δ^34S值变化最小,为-0.1‰- 4.2‰。而白龙厂矿床中硫化物的δ^34S值为-14.3‰--3.6‰。水泄和白龙厂矿床中重晶石的δ^34S值分别为 12.3‰- 19.0‰和 13.1‰,它们与盆地中蒸发岩层中石膏的δ^34S值( 10.8‰- 15.7‰)相近。分析表明,兰坪-思茅盆地中脉状铜矿的硫源主要来源于盆地热卤水萃取的地层中蒸发岩硫酸盐,它们通过有机质的热分解反应还原为沉淀硫化物所必需的低价硫。各矿床独特的硫同位素组成还表明它们的硫源受局部地层硫源和成矿流体物理化学性质所控制。本文提出大气降水起源的盆地热卤水通过对围岩中新生代地层的淋滤和萃取,获得了成矿所需的金属和硫,并在构造薄弱部位沉淀形成了本区的脉状铜矿床。  相似文献   
132.
133.
Abstract   The West Kunlun mountain range along the northwestern margin of the Tibetan Plateau is crucial in understanding the early tectonic history of the region. It can be divided into the North and South Kunlun Blocks, of which the former is considered to be part of the Tarim Craton, whereas consensus was not reached on the nature and origin of the South Kunlun Block. Samples were collected from the 471 Ma Yirba Pluton, the 405 Ma North Kudi Pluton and the 214 Ma Arkarz Shan Intrusive Complex. These granitoids cover approximately 60% of the Kudi area in the South Kunlun Block. Sr, Nd, and O isotope compositions preclude significant involvement of mantle-derived magma in the genesis of these granitoids; therefore, they can be used to decipher the nature of lower–mid crust in the area. All samples give Mesoproterozoic Nd model ages (1.1–1.5 Ga) similar to those of the exposed metamorphic complex of this block but significantly different from those of the basement of the North Kunlun Block (2.8 Ga). This indicates that the South Kunlun Block does not have an Archean basement, and, thus, does not support the microcontinent model that suggests the South Kunlun Block was a microcontinent once separated from and later collided back with the North Kunlun Block.  相似文献   
134.
For Central Greenland, water isotope analysis indicates a temperature difference of about 10°C since the Last Glacial Maximum (LGM). However, borehole thermometry and gas diffusion thermometry indicate that LGM surface temperatures were about 20°C colder than today. Two general circulation model studies have shown that changes in the seasonal precipitation timing in Central Greenland might have caused a warm bias in the LGM water isotope proxy temperatures, and that this bias could explain the difference in the estimated paleotemperatures. Here we present an analysis of a number of atmospheric general circulation model simulations mostly done within the framework of the Paleoclimate Modeling Intercomparison Project. The models suggest that the seasonal cycle of precipitation and surface mass balance over Central Greenland at the LGM might have been very different from today. This supports the idea that the accuracy of the water isotope thermometry at the LGM in Greenland might be compromised as a result of a modified surface mass balance seasonality. However, the models disagree on the amplitude and sign of the bias. For Central East Antarctica, a strong seasonality effect on the LGM isotopic signal is not simulated by any of the analyzed models. For the mid-Holocene (6 kyr BP) the models suggest relatively weak isotope paleothermometry biases linked to changes in the surface mass balance seasonality over both ice sheets.  相似文献   
135.
In an attempt to determine the helium and neon isotopic composition of the lower oceanic crust, we report new noble gas measurements on 11 million year old gabbros from Ocean Drilling Program site 735B in the Indian Ocean. The nine whole rock samples analyzed came from 20 to 500 m depth below the seafloor. Helium contents vary from 3.3×10−10 to 2.5×10−7 ccSTP/g by crushing and from 5.4×10−8 to 2.4×10−7 ccSTP/g by melting. 3He/4He ratios vary between 2.2 and 8.6 Ra by crushing and between 2.9 and 8.2 by melting. The highest R/Ra ratios are similar to the mean mid-ocean ridge basalt (MORB) ratio of 8±1. The lower values are attributed to radiogenic helium from in situ α-particle production during uranium and thorium decay. Neon isotopic ratios are similar to atmospheric ratios, reflecting a significant seawater circulation in the upper 500 m of exposed crust at this site. MORB-like neon, with elevated 20Ne/22Ne and 21Ne/22Ne ratios, was found in some high temperature steps of heating experiments, but with very small anomalies compared to air. These first results from the lower oceanic crust indicate that subducted lower oceanic crust has an atmospheric 20Ne/22Ne ratio. Most of this neon must be removed during the subduction process, if the ocean crust is to be recirculated in the upper mantle, otherwise this atmospheric neon will overwhelm the upper mantle neon budget. Similarly, the high (U+Th)/3He ratio of these crustal gabbros will generate very radiogenic 4He/3He ratios on a 100 Ma time scale, so lower oceanic crust cannot be recycled into either MORB or oceanic island basalt without some form of processing.  相似文献   
136.
The carbon isotope measurements, carried out on subsurface carbonate samples from Oxfordian Jaisalmer Formation, western India, yield positive d13C values up to +3.17%. The most positive Oxfordian C-isotope value corresponds to the carbon isotope excursion measured in samples from from other late Jurassic basins of world. The latest Oxfordian C-isotope values of Jaisalmer Basin fluctuate around 2% while the C-isotope values of 1.50% mark the base of Kimmeridgian. The Oxfordian C-isotope excursion appears to correspond to a time of overall increased organic carbon burial triggered by increased nutrient transfer from continents to oceans during a time of rising global sea level.  相似文献   
137.
Natural production of the radionuclide chlorine-36 (36Cl) has provided a valuable tracer for groundwater studies. The nuclear industry, especially the testing of thermonuclear weapons, has also produced large amounts of 36Cl that can be detected in many samples of groundwater. In order to be most useful in hydrologic studies, the natural production prior to 1952 should be distinguished from more recent artificial sources. The object of this study was to reconstruct the probable preanthropogenic levels of 36Cl in groundwater in the United States. Although significant local variations exist, they are superimposed on a broad regional pattern of 36Cl/Cl ratios in the United States. Owing to the influence of atmospherically transported ocean salt, natural ratios of 36Cl/total Cl are lowest near the coast and increase to a maximum in the central Rocky Mountains of the United States. Electronic Publication  相似文献   
138.
Oscillatory zoning in low δ18O skarn garnet from the Willsboro wollastonite deposit, NE Adirondack Mts, NY, USA, preserves a record of the temporal evolution of mixing hydrothermal fluids from different sources. Garnet with oscillatory zoning are large (1–3 cm diameter) euhedral crystals that grew in formerly fluid filled cavities. They contain millimetre‐scale oscillatory zoning of varying grossular–andradite composition (XAdr = 0.13–0.36). The δ18O values of the garnet zones vary from 0.80 to 6.26‰ VSMOW and correlate with XAdr. The shape, pattern and number of garnet zones varies from crystal to crystal, as does the magnitude of the correlated chemistry changes, suggesting fluid system variability, temporal and/or spatial, over the time of garnet growth. The zones of correlated Fe content and δ18O indicate that a high Fe3+/Al, high δ18O fluid mixed with a lower Fe3+/Al and δ18O fluid. The high δ18O, Fe enriched fluids were likely magmatic fluids expelled from crystallizing anorthosite. The low δ18O fluids were meteoric in origin. These are the first skarn garnet with oscillatory zoning reported from granulite facies rocks. Geochronologic, stable isotope, petrologic and field evidence indicates that the Adirondacks are a polymetamorphic terrane, where localized contact metamorphism around shallowly intruded anorthosite was followed by a regional granulite facies overprint. The growth of these garnet in equilibrium with meteoric and magmatic fluids indicates an origin in the shallow contact aureole of the anorthosite prior to regional metamorphism. The zoning was preserved due to the slow diffusion of oxygen and cations in the large garnet and protection from deformation and recrystallization in zones of low strain in thick, rigid, garnetite layers. The garnet provide new information about the hydrothermal system adjacent to the shallowly intruded massif anorthosite that predates regional metamorphism in this geologically complex, polymetamorphic terrane.  相似文献   
139.
Fluorine, chlorine, bromine, iodine and sulfur were determined in seventeen geological reference materials after extraction by pyrohydrolysis. Fluorine, Cl and S (as sulfate ions) were determined in the extraction solution by ion chromatography with detection limits of around 0.2 mg l−1. Bromine and I were measured by ICP-MS with detection limits of 1 μg l−1 for Br and 0.1 μg l−1 for I. For rock samples, using normal extraction conditions (500 mg of sample and 100 ml of final solution) detection limits were 40 mg kg−1 for F and Cl, 15 mg kg−1 for S, 0.2 mg kg−1 for Br and 0.02 mg kg−1 for I. These detection limits may be improved by increasing the amount of sample and hence the concentration of the final solution. Water was also determined using an extraction technique based on H2O degassing, reduction on zinc at 1000 °C and H2 manometry. Our results for fluorine, chlorine, sulfur and water are in good agreement with literature data. Very few reference materials have recommended values for bromine and especially for iodine. Among the analysed samples, three are new reference materials: BHVO-2, BCR-2 and AGV-2.  相似文献   
140.
Abstract. The petrography, chemical, fluid inclusion and isotope analyses (O, Rb-Sr) were conducted for the shale samples of the Mount McRae Shale collected from the Tom Price, Newman, and Paraburdoo mines in the Hamersley Basin, Western Australia. The Mount McRae Shale at these mines occurs as a footwall unit of the secondary, hematite-rich iron ores derived from the Brockman Iron Formation, one of the largest banded iron formations (BIFs) in the world. Unusually low contents of Na, Ca, and Sr in the shales suggest that these elements were leached away from the shale after deposition. The δ18O (SMOW) values fall in the range of + 15.0 to +17.9 per mil and show the positive correlation with calculated quartz/sericite ratios of the shale samples. This suggests that the oxygen isotopic compositions of shale samples were homogenized and equilibrated by postdepositional event. The pyrite nodules hosted by shales are often rimmed by thin layers of silica of varying crystallinity. Fluid inclusions in quartz crystals rimming a pyrite nodule show homogenization temperatures ranging from 100 to 240C for 47 inclusions and salinities ranging from 0.4 to 12.3 wt% NaCl equivalent for 18 inclusions. These fluid inclusion data give direct evidence for the hydrothermal activity and are comparable to those of the vein quartz collected from the BIF-derived secondary iron ores (Taylor et al, 2001). The Rb-Sr age for the Mount McRae Shale is 1,952 ± 289 Ma and at least 200 million years younger than the depositional age of the Brockman Iron Formation of ∼ 2.5 Ga in age. All the data obtained in this study are consistent with the suggestion that high temperature hydrothermal fluids were responsible for both the secondary iron ore formation and the alteration of the Mount McRae Shale.  相似文献   
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