全文获取类型
收费全文 | 14804篇 |
免费 | 3410篇 |
国内免费 | 5002篇 |
专业分类
测绘学 | 1977篇 |
大气科学 | 2859篇 |
地球物理 | 3202篇 |
地质学 | 8412篇 |
海洋学 | 2748篇 |
天文学 | 437篇 |
综合类 | 1315篇 |
自然地理 | 2266篇 |
出版年
2024年 | 113篇 |
2023年 | 306篇 |
2022年 | 854篇 |
2021年 | 1007篇 |
2020年 | 802篇 |
2019年 | 950篇 |
2018年 | 872篇 |
2017年 | 808篇 |
2016年 | 867篇 |
2015年 | 916篇 |
2014年 | 1011篇 |
2013年 | 1228篇 |
2012年 | 1260篇 |
2011年 | 1295篇 |
2010年 | 1232篇 |
2009年 | 1158篇 |
2008年 | 1163篇 |
2007年 | 1120篇 |
2006年 | 1007篇 |
2005年 | 878篇 |
2004年 | 657篇 |
2003年 | 542篇 |
2002年 | 559篇 |
2001年 | 528篇 |
2000年 | 375篇 |
1999年 | 334篇 |
1998年 | 222篇 |
1997年 | 199篇 |
1996年 | 182篇 |
1995年 | 158篇 |
1994年 | 116篇 |
1993年 | 107篇 |
1992年 | 84篇 |
1991年 | 50篇 |
1990年 | 46篇 |
1989年 | 49篇 |
1988年 | 28篇 |
1987年 | 16篇 |
1986年 | 17篇 |
1985年 | 19篇 |
1984年 | 9篇 |
1983年 | 13篇 |
1982年 | 6篇 |
1981年 | 8篇 |
1980年 | 5篇 |
1979年 | 8篇 |
1978年 | 7篇 |
1977年 | 5篇 |
1958年 | 4篇 |
1957年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
31.
Mauro Lo Cascio Yan Liang Nobumichi Shimizu Paul C. Hess 《Contributions to Mineralogy and Petrology》2008,156(1):87-102
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 P–T 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
32.
Yan Liang 《Geochimica et cosmochimica acta》2008,72(15):3804-3821
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
33.
Kathleen A. Radloff Anya R. Manning Brian Mailloux Yan Zheng M. Moshiur Rahman M. Rezaul Huq Kazi M. Ahmed Alexander van Geen 《Applied Geochemistry》2008
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
34.
淡水双壳类壳体碳同位素研究:以河蚬(corbicula fluminea,Müller 1774)为例 总被引:2,自引:0,他引:2
双壳类壳体碳酸盐(文石)稳定同位素组成已被广泛地用于古气候和古环境重建研究中,但是双壳类壳体碳同位素组成所指示的气候和环境意义一直是争议的问题.对双壳类河蚬(corbicula fluminea)进行了室内养殖,并选取两个壳体样品(壳高,A=13 mm,B=9mm),测定其生长部分壳体和生长期间水体碳同位素,研究表明,随着水体碳同位素的升高(δ13CDIC由-5.24‰升至1.41‰),两壳体碳同位素也随之升高,表明水体对壳体碳同位素的影响;δ13CA分布范围为-4.76‰~2.09‰,δ13CB为-8.49‰~2.89,壳体A和B碳同位素均比预测平衡值偏负,表明壳体在形成过程中利用了新陈代谢产生的富集12C的CO2.根据计算壳体A在实验中沉淀部分壳体利用新陈代谢碳的比例(M值)为24%~43%,平均值为33%;壳体B为33%~75%,平均值为58%.M值随生物的生长呈下降变化,这说明在实验中河蚬主要是通过增加对DIC的吸收和利用来满足壳体生长对物质量增加的需求. 相似文献
35.
贵州普定陈旗堡地区土体主要理化性质与持水量相关性研究 总被引:2,自引:0,他引:2
根据贵州普定陈旗堡典型喀斯特地区的生态特性,从水文地质与工程地质角度,借助土壤学对土壤水分特性的研究理论,对表层土壤20cm以下土层的土体物理化学性质与土体水分含量,即土体的持水量(waterholding capacity),进行了相关性研究。分析结果表明:土体颗粒成分、孔隙比、矿物成分含量等对土体水分含量均有影响。土体中粉粒含量较高而粘粒含量较少,且粒度分配不均匀时,土体水分含量相对较高;孔隙率高的土体水分含量较高;伊蒙混层矿物、伊利石和绿泥石等粘土矿物含量较高时,土体水分含量相对较高,而长石、碳酸盐等原生矿物含量较高时,土体水分含量相对较小。石英对于土体持水量影响不明显。 相似文献
36.
37.
38.
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
39.
贡嘎山海螺沟冰川径流水文规律的同位素示踪研究 总被引:3,自引:1,他引:2
应用同位素地球化学的基本原理和示踪技术, 对贡嘎山海螺沟冰川河源区和干流的不同区段, 不同时域径流的组成特点及其水文动态变化规律进行分析研究.结果表明: 贡嘎山海螺沟冰川河源区水的组成, 不同季节、不同时段(早、晚)有明显的变化. 夏季晚上的水大约有82.4%是来自冰川区的水, 17.6%为非冰川区的径流; 早晨中的水来自冰川区的占74.6%, 非冰川区径流占25.4%. 冰川消融水的最大可占总水量的6.9%~7.8%左右. 在冬季时段, 冰舌末端排泄水(BCH-1)和冰川水文站(HLG-6)径流的同位素组成均低于底部冰川冰(BCB-2: -16.639‰), 显示出严重同位素不平衡的特点, 反映了冬季底部冰川消融水在源区水(BCH-1)中的贡献已达很低的程度, 而代之以冰川上部占主导优势的雨雪水. 这意味着在冬季当地冰川的退缩速度与夏季相比有明显减慢的趋势. 示踪表明, 在冰川水文站附近区域内存在水的渗漏, 夏季可能延伸到倒中桥(HLG-13采样点上方)一带, 下渗水通过地下通道, 到杉树坪(HLG-2采样点)邻近的区域回补到河道内. 相似文献
40.
在柴达木盆地北缘地区,分别选取有机碳含量很低和较高的侏罗系泥岩样品,对比分析了它们在生物标志物组成上的差异。结果发现,高有机质丰度泥岩的生标组成与我国西北地区侏罗纪煤系有机质的特征差异不大,相比而言,低有机质丰度泥岩的正烷烃以前主峰为特征,Pr/Ph比值在1.0左右,三环萜烷和伽马蜡烷丰度较高,并在部分样品中检出了25 降藿烷系列。结合泥岩的有机岩石学特征,认为这些差异可能反映了泥岩沉积环境和生烃母质的不同:高有机质丰度泥岩的有机显微组分以相对弱还原条件下的形态有机质为主,包括藻类体、孢子体和角质体等,而低有机质丰度泥岩的有机显微组分以相对强还原条件下的矿物沥青基质为主,其母质可能来源于低等显微菌藻类。进一步通过对比不同有机质丰度泥岩,以及区内原油生标组成之间的相互关系,讨论了研究区的油源问题。 相似文献