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111.
内蒙古巴彦塔拉盆地砂岩型铀矿化的蚀变特征   总被引:1,自引:0,他引:1  
巴彦塔拉盆地砂岩型铀矿床产于下白垩统赛汉塔拉组下段辫状河流相砂岩中。本文通过对含矿主岩沉积特征、矿化和矿床蚀变特征的分析研究 ,认为早期为潜水氧化蚀变成矿 ;晚期为层间氧化 油气还原蚀变成矿 ,即来自蚀源区和天窗补给的含铀、含氧地下水遇沿断裂 (F2 1)上升的含H2 S的油气还原叠加改造成矿  相似文献   
112.
鄂尔多斯深盆气与铀矿化关系初探   总被引:24,自引:4,他引:24  
张如良 《铀矿地质》2004,20(4):213-218,234
深盆气是非常规的天然气藏。鄂尔多斯深盆气与铀矿化有密切关系,上古生界气源层铀含量丰富、易浸出,故也为铀源层。在铀源层成岩时所形成的压榨水(即深层水),经燕山期热事件快速增温增压,使铀的溶解度大大增加。此时也正是盆地生气高峰期,气压远远大于水压,气体推动深层水沿断裂向上扩散。在上覆透水层,由于地表水的参与形成复杂的气水地球化学垒,使铀沉积成矿。本文还总结了该类型铀矿的找矿准则。  相似文献   
113.
油气圈闭与鄂尔多斯盆地北部铀成矿关系探讨   总被引:11,自引:2,他引:11  
鄂尔多斯盆地北部的伊盟隆起区 ,特别是杭锦旗至东胜一带的地层发育大量的圈闭 ,它们是油气聚集成藏的场所。本文剖析了这些圈闭的类型和成因 ,指出它们是盆地北部天然气运移的有利指向区 ,是还原性气体的储存库和重要的扩散源 ;油气渗出和含氧含铀水渗入的交汇部位是铀成矿的有利场所。因此 ,查明圈闭和断裂构造 ,对分析油气运移方向及砂岩型铀矿预测具有实际意义  相似文献   
114.
钱家店铀矿床U-Ra平衡系数特征研究   总被引:1,自引:0,他引:1  
本文探讨了可地浸砂岩型铀矿U-Ra平衡系数的计算方法,研究了钱家店砂岩型铀矿床U-Ra平衡系数的变化特征。这些成果为钱家店铀矿床放射性测井数据的修正、矿体边界的确定、铀矿资源量的计算提供了科学依据。  相似文献   
115.
江苏泥炭大多数为低有机质分解较强的低位泥炭,适于制作肥料或制成腐肥使用;江苏硅质原料丰富,一种以硅为主的化肥——硅肥正日益显示其重要性;湖泊淤泥具有颗粒微细、含砂量少、可塑性高、结合力强、干燥敏感性好和收缩率较大等特点,是生产空心砖的最佳原料;高家边组泥页岩和坟头组底部细粉砂质泥岩及泥质粉砂岩是良好的陶粒原料、砖瓦、陶瓷建材以及水泥用粘土质原料;利用矿泉水与茶的结合能够生产出高、中、低多效应的复合型新产品。上述尚未被利用或利用程度不够的矿产资源有着广泛的开发利用前景。  相似文献   
116.
云南白秧坪地区是以银、钴多金属矿化为特色的矿集区,成矿作用与兰坪盆地两侧的推覆构造系统密切相关,发育一套复杂的中低温热液矿物组合,出现了铜、钴、镍、铋等亲地幔元素的硫化物(硫钴镍矿、硫铋铜矿),显示地幔深源物质可能参与了成矿作用。银、钴赋存状态的初步研究表明载银矿物主要为汞银矿、辉银矿、银黝铜矿、方铅矿、黝铜矿及砷、锑、铅硫盐矿物等,载钴矿物主要为硫钴镍矿、辉砷钴矿、含钴毒砂等硫化物。  相似文献   
117.
Sixteen kimberlite boulders were collected from three sites on the Munro and Misema River Eskers in the Kirkland Lake kimberlite field and one site on the Sharp Lake esker in the Lake Timiskaming kimberlite field. The boulders were processed for heavy-mineral concentrates from which grains of Mg-ilmenite, chromite, garnet, clinopyroxene and olivine were picked, counted and analyzed by electron microprobe. Based on relative abundances and composition of these mineral phases, the boulders could be assigned to six mineralogically different groups, five for the Kirkland Lake area and one for the Lake Timiskaming area. Their indicator mineral composition and abundances are compared to existing data for known kimberlites in both the Kirkland Lake and Lake Timiskaming areas. Six boulders from the Munro Esker form a compositionally homogeneous group (I) in which the Mg-ilmenite population is very similar to that of the A1 kimberlite, located 7–12 km N (up-ice), directly adjacent to the Munro esker in the Kirkland Lake kimberlite field. U–Pb perovskite ages of three of the group I boulders overlap with that of the A1 kimberlite. Three other boulders recovered from the same localities in the Munro Esker also show some broad similarities in Mg-ilmenite composition and age to the A1 kimberlite. However, they are sufficiently different in mineral abundances and composition from each other and from the A1 kimberlite to assign them to different groups (II–IV). Their sources could be different phases of the same kimberlite or—more likely—three different, hitherto unknown kimberlites up-ice of the sample localities along the Munro Esker in the Kirkland Lake kimberlite field. A single boulder from the Misema River esker, Kirkland Lake, has mineral compositions that do not match any of the known kimberlites from the Kirkland Lake field. This suggests another unknown kimberlite exists in the area up-ice of the Larder Lake pit along the Misema River esker. Six boulders from the Sharp Lake esker, within the Lake Timiskaming field, form a homogeneous group with distinct mineral compositions unmatched by any of the known kimberlites in the Lake Timiskaming field. U–Pb perovskite age determinations on two of these boulders support this notion. These boulders are likely derived from an unknown kimberlite source up-ice from the Seed kimberlite, 4 km NW of the Sharp Lake pit, since indicator minerals with identical compositions to those of the Sharp Lake boulders have been found in till samples collected down-ice from Seed. Based on abundance and composition of indicator minerals, most importantly Mg-ilmenite, and supported by U–Pb age dating of perovskite, we conclude that the sources of 10 of the 16 boulders must be several hitherto unknown kimberlite bodies in the Kirkland Lake and Lake Timiskaming kimberlite fields.  相似文献   
118.
An experimental study on reduction of U (Ⅵ) by anaerobic bacteria, Shewane//a putrefaciens, is first reported here in China. The experimental conditions were: 35℃ and pH =7.0-7.4, corresponding to a physicochemical environments in which the sandstone-hosted interlayer oxidation-zone type uranium deposit formed in Northwest China's Xinjiang. Bacteria adopted in the present experiment, Shewanella putrefaciens, occur extensively in natural environment. Our study shows that nano-crystal precipitates of uraninite quickly occurred on the surface of the cells within one week. It was found that the pitchblende was characterized by a random arrangement of uraninite nanocrystals (2-4 nm) in it, significantly different from natural pitchblende in which uraninite nanocrystals are arranged in order. Finally, a possible mechanism of uranium biomineralization by microorganisms in the deposits is discussed. Our investigation may supply a technical train of thoughts for bioremediation of nuclear-contaminated water environments and for underground dissolving extraction of the sandstone-hosted uranium ores.  相似文献   
119.
Biomineralization of Uranium: A Simulated Experiment and Its Significance   总被引:5,自引:0,他引:5  
A simulated experimental reduction of U^v1 and the synthesis of uraninite by a sulfate-reducing bacteria,Desulfovibrio desulfuricans DSM 642, are first reported. The simulated physicochemical experimental conditions were:35℃, pH=7.0-7.4, corresponding to the environments of formation of the sandstone-hosted interlayer oxidation-zone type uranium deposits in Xinjiang, NW China. Uraninite was formed on the surface of the host bacteria after a one-week‘s incubation. Therefore, sulfate-reducing bacteria, which existed extensively in Jurassic sandstone-producing environments,might have participated in the biomineralization of this uranium deposit. There is an important difference in the orderdisorder of the crystalline structure between the uraninite produced by Desulfovibrio desulfuricans and naturally occurring uraninite. Long time and slow precipitation and growth of uraninite in the geological environment might have resulted in larger uraninite crystals, with uraninite nanocrystals arranged in order, whereas the experimentally produced uraninite is composed of unordered uraninite nanocrystals which, in contrast, result from the short time span of formation and rapid precipitation and growth of uraninite. The discovery has important implications for understanding genetic significance in mineralogy, and also indicates that in-situ bioremediation of U-contaminated environments and use of biotechnology in the treatment of radioactive liquid waste is being contemplated.  相似文献   
120.
Experimental studies on the interactions between artificial seawater (ASW) and fresh rhyolite, perlite and weakly altered dacitic tuff containing a small amount of smectite suggest changing cation transfer during smectite-forming processes. Initially, dissolution of K from the rocks accompanies incorporation of Mg and Ca from ASW during both earlier (devitrification stage) and later smectite formation, whereas Ca incorporated with early smectite formation redissolves with progressive reaction. Barium mobility increases toward the later smectite-forming reactions. Therefore, the large amounts of barite, anhydrite and gypsum in Kuroko ore deposits are considered to have precipitated from hydrothermal solutions derived from the interaction with previously altered felsic rocks during late smectite formation, rather than by the reaction with fresh felsic rocks.Editorial handling: D. Lentz  相似文献   
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