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101.
库车盆地西北缘下第三系碳、氧同位素特征及成岩环境   总被引:3,自引:0,他引:3  
傅启龙 《地层学杂志》1996,20(4):280-284
库车盆地西北缘及柯坪地区下第三系碳酸盐岩稳定同位素分析结果显示氧同位素组成在相对较小的范围内变化,而碳同位素组成变化很大。沉积学研究表明塔拉克组和小库孜拜组海相地层主要为潮坪、萨布哈和渴湖相沉积,在成岩过程中或成岩期后,沉积物不同程度地受到了淡水作用的影响。所分析的样品大部分形成于大气淡水成岩环境,富集12C,δ13C为正值的样品一般形成于海水成岩环境。稳定同位素分析是研究成岩作用的有效手段之一。  相似文献   
102.
新疆苏吉泉石墨矿床成因的碳同位素证据   总被引:13,自引:0,他引:13  
张国新  胡霭琴 《地球化学》1996,25(4):379-386
新疆苏吉泉石墨矿床产在海西期花岗岩体中,矿石具十分独特的球状构造,石墨的δ13C值分布范围为-20.5‰-23.9‰,平均值为-22.0‰,表明该石墨矿床碳质的有机成因。围岩中特别是中石碳统的含碳沉积岩被海西中期花岗岩岩浆同化,使碳质聚集并重结晶成石墨。  相似文献   
103.
黑色岩系中铂族元素地质地球化学特征   总被引:6,自引:0,他引:6  
含PGE黑色岩系可根据黑色岩系中有无火成岩,将其分为:(1)与火山作用或岩浆活动无关的黑色岩系;(2)与火山作用或岩浆活动有关的黑色岩系不同地质背景下,富金属黑色岩系的特征及其PGE的分布特征既有相似之处,又各具特点,反映出两者PGE的地球化学演化过程有所差别。有关PGE比值不仅可以反映出元素的地球化学行为,亦可区分或指示不同环境下PGE地球化学演化的规律性。  相似文献   
104.
面向21世纪的煤化工   总被引:8,自引:0,他引:8  
煤炭是中国的主要能源和资源,但同时也是主要的污染源。从保护环境、合理利用有限的化石资源的角度和中国的具体国情考虑,应该大力开发温和化高效煤的新工艺,使煤炭资源逐步由能源型利用转化为材料型利用,近年来,我们在煤的溶剂萃取,脱硫降灰机理,煤相关模型化合物反应,煤焦油中稠环芳香族化合物的分离精制,功能性高分子单体合成及一氧化碳高效吸附剂的制备等方面做了大量的研究工作,结合这些研究工作,本文介绍了煤化工的  相似文献   
105.
李儒峰  刘本培 《地质学报》1996,70(4):342-350
应用层序地层学理论对黔南独山地区晚石炭世麦粒链带地层进行了详细的沉积层序分析和系统的碳同位素测定,识别出2个三级沉积层序和17个准层序,其可与北美中大陆同期地层中发现的2个三级沉积层序和17个亚层序对比,是晚石炭世Gzhelian期存在全球沉积记录同时性的佐证。同时探讨了碳同位素演化与全球海平面变化之间的内在联系,总结出沉积层序内碳同位素演化规律。  相似文献   
106.
This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg–1 pH of 7.6 and p(CO2) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg–1, pH of 7.70 and p(CO2) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO2) up to 5.6 times the atmospheric P(CO2).  相似文献   
107.
 The amounts and types of extractable hydrocarbon components in sediment cores from the Rochester Basin of eastern Lake Ontario provide a record of environmental changes that have accompanied the settlement and population growth of the surrounding land areas. Sediments deposited prior to the mid-1800s contain low concentrations of hydrocarbons that are dominated by land-plant wax components. Concentrations begin to rise in the late 1800s as erosion of soil and nutrients from watershed areas accelerated. This pattern continues into modern times. Episodes of enhanced aquatic productivity are sometimes recorded in twentieth-century sediments by the dominance of algal hydrocarbons, but land-plant components typically predominate. Petroleum residues begin to appear in sediments deposited in the late 1800's but remain minor constituents of the hydrocarbon contents of modern sediments in the Rochester Basin. Received: 21 March 1995 · Accepted: 11 August 1995  相似文献   
108.
华南西部晚二叠世碳同位素地层学研究   总被引:1,自引:1,他引:1  
对黔桂地区7条晚二叠世碳酸盐岩型煤系剖面进行了碳酸盐岩碳氧同位素测定,发现晚二叠世吴家坪阶与长兴阶碳酸盐岩的δ13C值有明显差异,前者δ13C多大于3.0‰,后者多小于3.0‰,进一步对晚二叠世δ13C的变化原因的分析表明,δ13C的变化可能与晚古生代末期聚煤作用的减弱密切相关,后者造成自然界碳库中的12C的富集,从而使得海水以及在其中沉淀出的碳酸盐岩中的δ13C值降低。此外,植物光合作用从大气中吸收CO2的量也随陆地植被减少而减少,结果造成大气中的CO2的大量富集,从而进一步产生温室效应,制约生物界的发展。联系到这一阶段生物界的衰亡灭绝,可以认为温室效应是晚二叠世生物逐渐衰亡及晚二叠世末群体灭绝的主要原因之一。  相似文献   
109.
 Acidification of groundwater lags behind acid deposition due to the relatively long water residence time in conjunction with various buffering processes in the soil zone and deeper aquifer (chemical weathering, cation exchange, sulfate sorption, and N uptake by the biomass). Extensive field data from eight forested catchments in the Bunter Sandstone of the Black Forest, including results from water budget studies and hydrochemical analysis of stream and spring waters, were used to simulate the future evolution of ground-water acidification with the MAGIC model. The present acid deposition exceeds the “critical load” (here meaning buffering due to chemical weathering and protonation of organic acids) in six of eight catchments. Two catchments are well buffered because they contain carbonate-bearing layers in the Upper Bunter sandstone. Transient buffering (i.e., cation exchange, N uptake, the sulfate sorption) thus far prevents worse acidification, but this effect will decline in the future. For one of the poorly buffered catchments (Seebach), a two-layer simulation was carried out, based on extensive data from 10 years of measurements. Validation of the long-term simulations by hydrochemical and soil data was hampered by strong annual variations but generally supported by paleolimnological studies. In the future, reductions in the S deposition by 20% and the N deposition by 10% up to the year 2030 are assumed as the most probable scenario. N uptake through soil and vegetation will come to an end as suggested by decreasing C/N ratios of the organic matter. This process is arbitrarily included in the simulations. In the periglacial soil layer, acidification will decrease until the year 2030 and then approach a steady-state condition. In the fractured aquifer, acidification will also proceed at a decreasing rate; however, sulfate desorption up to the year 2130, the end of simulated period, will prevent earlier remediation. Despite a significant reduction in S deposition since the mid-1980s, further efforts are necessary to reduce the emission of acidifying substances. Liming in the recharge area is partially effective to ameliorate “shallow” groundwater but largely fails to ameliorate “deeper” groundwater in the sandstone aquifer. Received: 30 July 1996/Accepted: 23 January 1997  相似文献   
110.
 This paper examines the cause of color variations of trachytic pumices which are essentially uniform in chemical composition and proposes a geological model for their formation. A pyroclastic sequence of distinct subunits with brown, buff, and black pumices was deposited during the 5000-B.P. eruption of a tuff ring in the central Meidob volcanic field (Sudan). Subunits of buff pumices locally contain minor amounts of streaky pumice with pale-gray and dark-gray domains. The combined evidence of petrographic studies, chemical analyses of whole pumices and groundmass separates, electron microprobe analyses, optical spectroscopy, transmission electron microscopy, and magnetic susceptibility measurements show that color variations of the pumice clasts are related to the size and distribution of Fe3+-rich oxide microcrysts. Buff pumice and light-gray domains of streaky pumice have a colorless, transparent groundmass with very few microcrysts. Dark-gray domains of streaky pumice contain abundant hematite and/or magnetite microcrysts visible in thin section within a transparent, colorless glass groundmass. The groundmass of the black pumice clasts is brown in thin section which is most likely caused by submicroscopic magnetite microcrysts. Brown pumice clasts have a mixed groundmass consisting of brown domains and domains with opaque microcrysts in transparent glass. Variations in the eruption dynamics have been inferred from lithological observations. Subunits of black pumices are related to eruption pulses with low magma discharge and high water/magma mass ratio, whereas subunits of buff pumice were deposited during eruption pulses with high magma discharge and low water/magma mass ratio. Brown pumices represent the top part of the magma body, and the initial stage of the eruption probably had a low magma discharge. Streaky pumices are interpreted as the product of syn-eruptive mixing of Fe3+-rich oxide microcryst-bearing magma and microcryst-free magma. Received: 3 February 1997 / Accepted: 28 July 1997  相似文献   
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