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41.
The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar PT conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   
42.
Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle.  相似文献   
43.
Microbial Fe reduction is widely believed to be the primary mechanism of As release from aquifer sands in Bangladesh, but alternative explanations have been proposed. Long-term incubation studies using natural aquifer material are one way to address such divergent views. This study addresses two issues related to this approach: (1) the need for suitable abiotic controls and (2) the spatial variability of the composition of aquifer sands. Four sterilization techniques were examined using orange-colored Pleistocene sediment from Bangladesh and artificial groundwater over 8 months. Acetate (10 mM) was added to sacrificial vials before sterilization using either (1) 25 kGy of gamma irradiation, (2) three 1-h autoclave cycles, (3) a single addition of an antibiotic mixture at 1× or (4) 10× the typical dose, and (5) a 10 mM addition of azide. The effectiveness of sterilization was evaluated using two indicators of microbial Fe reduction, changes in diffuse spectral reflectance and leachable Fe(II)/Fe ratios, as well as changes in P-extractable As concentrations in the solid phase. A low dose of antibiotics was ineffective after 70 days, whereas autoclaving significantly altered groundwater composition. Gamma irradiation, a high dose of antibiotics, and azide were effective for the duration of the experiment.  相似文献   
44.
按矿化特征将金川X矿区主矿体分为致密块状特富矿、海绵状富矿和浸染状贫矿.应用MicroMine软件对3类矿化体分别建立了数学模型,并应用距离平方反比法对模型单元块进行了镍、铜品位估值.通过分析和对比矿床数学模型900m至1300m不同水平剖面上的Ni、Cu品位及Ni/Cu比值的变化,得出在X矿区的中部西侧是一个Ni和Cu的矿化中心,并且向深部Cu的矿化强度高于Ni.  相似文献   
45.
碳酸盐岩裂缝与岩溶作用研究   总被引:12,自引:2,他引:10  
从构造与非构造作用角度出发,突出研究断层对裂缝的控制作用、断裂与岩溶的关系和裂缝与岩溶之间的关系,揭示碳酸盐岩裂缝与岩溶的发育规律。研究表明:构造裂缝为岩溶发育提供岩溶作用进行的有利通道,非构造裂缝则可以加速溶蚀作用的进行,促进岩溶的发育;裂缝与岩溶之间的关系始终是相辅相成、相互促进的关系。  相似文献   
46.
西藏马攸木金矿床金银互化物的赋存状态   总被引:3,自引:0,他引:3  
马攸木金矿床是西藏近年发现的首例规模较大、矿石品位富、金成色高的岩金矿床.作者通过对马攸木金矿床矿石组构、矿石共生组合及矿物特征研究发现,金银互化物主要有自然金、含银自然金、银金矿、自然银.载金矿物为黝铜矿、针铁矿、脆硫锑铅矿及石英;金银互化物的赋存形式主要为包裹体金、裂隙金及粒间金.金银互化物的形成、富集与热液成矿作用及表生风化作用关系密切.  相似文献   
47.
王猛  刘焰  何延波  魏东 《地质科学》2008,43(3):603-622
利用GTOPO30和SRTM3数字高程(DEM)数据,提取了喜马拉雅山脉(造山带)的数字高程模型并对其进行了地质地貌的初步分析。从SRTM3数字高程数据提取出坡度数据,初步分析了喜马拉雅山脉坡度和高程的特征。数字高程和坡度图清楚地展现了喜马拉雅大型断裂带(构造边界)的空间分布特征。分析了中国气象局下属的西藏、青海、四川和云南4省区气象观测台站55年来的年平均降水量观测数据、喜马拉雅山脉南坡的年平均降水量数据、喜马拉雅DEM和裂变径迹数据,发现喜马拉雅山脉从东至西,年平均降水量逐渐减少,地形起伏逐渐变小,而高程渐次升高,与此同时剥蚀速率降低;从北至南,年平均降水量逐渐增加,地形起伏增大,高程快速降低,而剥蚀速率则急剧升高。这充分说明了喜马拉雅年平均降水量大的地区,地表剥蚀作用相对较强,年平均降水量小的地区,地表剥蚀作用则较弱,即:在喜马拉雅地区,长周期的地表剥蚀过程(可长达数个百万年时间尺度)和短周期(仅仅50年)的降水量观测是耦合的。  相似文献   
48.
气候变化对塔里木河来自天山的地表径流影响   总被引:21,自引:10,他引:11  
塔里木河水资源主要来自天山南坡两条源流,选择西段阿克苏河和中段开都河-孔雀河作为研究区.1956-2003年研究河源山区气温呈持续升温且降水波动增加的趋势,其中1995-2003年升温强劲,升温速率高出48 a期间平均的3倍以上;降水自1986年后持续增加,20世纪90年代较80年代增幅达18%,并显示出河源山区湿岛向塔里木盆地扩展.因高山缺少气象观测,出山径流过程变化可以综合反映中高山带的气候变化.塔里木河来自天山的地表径流在1986-2003年间持续增长,以冰川融水补给为主的库玛拉克河,1994年以来年径流量增加已在前期平均值基础上提升了一个台阶;开都河以降水径流补给为主,1986-2002年出现了观测记录以来的丰水期,并使1986年后博斯腾湖水位快速上升,恢复到1958年记录的最高水位以上.两河年径流变化趋势基本相似,但也显示有西、中段的气候变化局部差异,出现丰枯水期的不一致;然而,在近16 a升温过程中,年径流增长幅度和快慢相近.  相似文献   
49.
在-25~ 25 ℃环境温度条件下, 采用水中冻融和空气中冻融两种方式, 经过50次冻融循环后, 在15 ℃、 0 ℃、 -10 ℃、 -20 ℃和-35 ℃工况下对土工格栅试样进行了拉伸性能的试验研究, 获得了聚乙烯塑料土工格栅的极限承载力、最大延伸率、 不同延伸率对应的应力值等数据. 试验结果表明, 聚乙烯塑料土工格栅在低温时抗拉性能明显提高, 从 15 ℃降至-35 ℃时, 5%延伸率对应的抗拉强度提高107%, 极限承载力提高19%. 同时, 聚乙烯塑料土工格栅极限延伸率随温度降低呈线形关系降低, 从 15 ℃降至-35 ℃时, 极限延伸率降低80%.  相似文献   
50.
青藏高原季节性冻土的时空分布特征   总被引:9,自引:4,他引:5  
利用青藏高原72个气象台站的冬季逐日冻结深度资料, 采用动力学Q指数和小波分析方法, 研究了青藏高原季节性冻土的时空变化特征. 结果发现: 青藏高原季节性冻土各站点相互间的动力学Q指数在高原大部分地区都比较小, 仅在高原南部部分站点值较大, 表明在高原上总体来说季节性冻土的动力学结构是一致的. 各站季节性冻土1980年代前后的Q指数在高原主体也都比较小, 只是在高原东南部和柴达木盆地的部分地区Q指数较大, 表明在高原大部分地区季节性冻土变化的动力学结构特征没有发生突变. 青藏高原季节性冻土总体上呈现下降趋势, 在20世纪80年代中期有一次均值突变, 突变以前的冬季平均冻结深度在93 cm左右, 突变以后的冬季平均冻结深度下降了10 cm左右. 高原季节性冻土冬季平均深度有准4 a的周期变化.  相似文献   
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