全文获取类型
收费全文 | 4179篇 |
免费 | 689篇 |
国内免费 | 1513篇 |
专业分类
测绘学 | 88篇 |
大气科学 | 250篇 |
地球物理 | 1053篇 |
地质学 | 3109篇 |
海洋学 | 680篇 |
天文学 | 673篇 |
综合类 | 190篇 |
自然地理 | 338篇 |
出版年
2024年 | 12篇 |
2023年 | 40篇 |
2022年 | 115篇 |
2021年 | 159篇 |
2020年 | 207篇 |
2019年 | 207篇 |
2018年 | 141篇 |
2017年 | 139篇 |
2016年 | 185篇 |
2015年 | 191篇 |
2014年 | 218篇 |
2013年 | 256篇 |
2012年 | 240篇 |
2011年 | 309篇 |
2010年 | 272篇 |
2009年 | 338篇 |
2008年 | 361篇 |
2007年 | 329篇 |
2006年 | 326篇 |
2005年 | 297篇 |
2004年 | 241篇 |
2003年 | 231篇 |
2002年 | 177篇 |
2001年 | 183篇 |
2000年 | 140篇 |
1999年 | 172篇 |
1998年 | 148篇 |
1997年 | 114篇 |
1996年 | 111篇 |
1995年 | 94篇 |
1994年 | 85篇 |
1993年 | 66篇 |
1992年 | 54篇 |
1991年 | 43篇 |
1990年 | 31篇 |
1989年 | 49篇 |
1988年 | 19篇 |
1987年 | 20篇 |
1986年 | 17篇 |
1985年 | 11篇 |
1984年 | 7篇 |
1983年 | 4篇 |
1982年 | 4篇 |
1981年 | 2篇 |
1979年 | 4篇 |
1978年 | 4篇 |
1977年 | 2篇 |
1976年 | 2篇 |
1974年 | 1篇 |
1971年 | 2篇 |
排序方式: 共有6381条查询结果,搜索用时 46 毫秒
31.
氢化物发生-原子荧光光谱法直接测定地球化学样品中痕量碲 总被引:2,自引:1,他引:1
采用硝酸-氢氟酸-高氯酸溶解样品,以Fe3+作减缓剂,不需分离富集,用氢化物发生-原子荧光光谱法直接测定地球化学样品中痕量碲。对测定介质、KBH4浓度、铁盐的作用等条件进行试验。方法检出限为0.0031μg/g,精密度(RSD,n=11)<6.10%。方法用于国家一级地球化学标准物质中痕量碲的测定,结果与标准值一致。 相似文献
32.
33.
34.
碱消解-高效液相色谱-电感耦合等离子体质谱法测定生物样品中的甲基汞和乙基汞 总被引:7,自引:2,他引:5
建立了碱消解-高效液相色谱-电感耦合等离子体质谱联用系统测定生物样品中甲基汞(MeHg)与乙基汞(EtHg)的分析方法。为提高灵敏度,选用微流量的PFA雾化器,在优化的检测条件下,MeHg及EtHg检出限可达到0.036μg/L和0.03μg/L;线性范围达到4个数量级,两条工作曲线线性相关系数为1。对1.78μg/L MeHg、1.65μg/L EtHg的混合标准溶液重复测定7次,色谱峰面积的相对标准偏差(RSD)分别为1.79%和1.44%。对标准物质BCR 464(金枪鱼)的分析结果表明,测定值与标准值基本吻合,但略低于标准值;甲基汞和乙基汞的加标回收率分别为85.9%和84.5%。高效液相色谱与质谱联用技术的高灵敏度和低检出限能够满足生物样品中汞形态定量分析的要求。 相似文献
35.
36.
Paul R. Craddock Olivier J. Rouxel Lary A. Ball Wolfgang Bach 《Chemical Geology》2008,253(3-4):102-113
We have developed a technique for the accurate and precise determination of 34S/32S isotope ratios (δ34S) in sulfur-bearing minerals using solution and laser ablation multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). We have examined and determined rigorous corrections for analytical difficulties such as instrumental mass bias, unresolved isobaric interferences, blanks, and laser ablation- and matrix-induced isotopic fractionation. Use of high resolution sector-field mass spectrometry removes major isobaric interferences from O2+. Standard-sample bracketing is used to correct for the instrumental mass bias of unknown samples. Background on sulfur masses arising from memory effects and residual oxygen-tailing are typically minor (< 0.2‰, within analytical error), and are mathematically removed by on-peak zero subtraction and by bracketing of samples with standards determined at the same signal intensity (within 20%). Matrix effects are significant (up to 0.7‰) for matrix compositions relevant to many natural sulfur-bearing minerals. For solution analysis, sulfur isotope compositions are best determined using purified (matrix-clean) sulfur standards and sample solutions using the chemical purification protocol we present. For in situ analysis, where the complex matrix cannot be removed prior to analysis, appropriately matrix-matching standards and samples removes matrix artifacts and yields sulfur isotope ratios consistent with conventional techniques using matrix-clean analytes. Our method enables solid samples to be calibrated against aqueous standards; a consideration that is important when certified, isotopically-homogeneous and appropriately matrix-matched solid standards do not exist. Further, bulk and in situ analyses can be performed interchangeably in a single analytical session because the instrumental setup is identical for both. We validated the robustness of our analytical method through multiple isotope analyses of a range of reference materials and have compared these with isotope ratios determined using independent techniques. Long-term reproducibility of S isotope compositions is typically 0.20‰ and 0.45‰ (2σ) for solution and laser analysis, respectively. Our method affords the opportunity to make accurate and relatively precise S isotope measurement for a wide range of sulfur-bearing materials, and is particularly appropriate for geologic samples with complex matrix and for which high-resolution in situ analysis is critical. 相似文献
37.
Gamma activity from the naturally occurring radionuclides namely, 226Ra, 232Th, the primordial radionuclide 40K was measured in the soil of Cuihua Mountain National Geological Park, China using γ-ray spectrometry technique. The mean
activity of 226Ra, 232Th and 40K were found to be 27.2 ± 6.5, 43.9 ± 6.2 and 653.1 ± 127.6 Bq kg−1, respectively. The concentrations of these radionuclides were compared with the typical world values and the average activities
of Chinese soil. The radium equivalent activity, the air absorbed dose rate, the annual effective dose rate, and the external
hazard index were evaluated and compared with the internationally approved values. All the soil samples have Raeq lower than the limit of 370 Bq kg−1 and H
ex less than unity. The overall mean outdoor terrestrial gamma dose rate is 66.3 nGy h−1 and the corresponding outdoor annual effective dose is 0.081 mSv. 相似文献
38.
D. J. Cherniak 《Physics and Chemistry of Minerals》2008,35(4):179-187
Self-diffusion of Si under anhydrous conditions at 1 atm has been measured in natural zircon. The source of diffusant for
experiments was a mixture of ZrO2 and 30Si-enriched SiO2 in 1:1 molar proportions; experiments were run in crimped Pt capsules in 1-atm furnaces. 30Si profiles were measured with both Rutherford backscattering spectrometry (RBS) and nuclear reaction analysis with the resonant
nuclear reaction 30Si(p,γ)31P. For Si diffusion normal to c over the temperature range 1,350–1,550°C, we obtain an Arrhenius relation D = 5.8 exp(−702 ± 54 kJ mol−1/RT) m2 s−1 for the NRA measurements, which agrees within uncertainty with an Arrhenius relation determined from the RBS measurements
[62 exp(−738 ± 61 kJ mol−1/RT) m2 s−1]. Diffusion of Si parallel to c appears slightly faster, but agrees within experimental uncertainty at most temperatures
with diffusivities for Si normal to c. Diffusion of Si in zircon is similar to that of Ti, but about an order of magnitude faster than diffusion of Hf and two
orders of magnitude faster than diffusion of U and Th. Si diffusion is, however, many orders of magnitude slower than oxygen
diffusion under both dry and hydrothermal conditions, with the difference increasing with decreasing temperature because of
the larger activation energy for Si diffusion. If we consider Hf as a proxy for Zr, given its similar charge and size, we
can rank the diffusivities of the major constituents in zircon as follows: D
Zr < D
Si << D
O, dry < D
O, ‘wet’. 相似文献
39.
M. Mejías J. Garcia-Orellana J. L. Plata M. Marina E. Garcia-Solsona B. Ballesteros P. Masqué J. López C. Fernández-Arrojo 《Environmental Geology》2008,54(3):521-536
A methodology for the characterization of deep carbonate aquifers has been developed and applied to El Maestrazgo Jurassic
aquifer in Castellón, Spain. Characterization of these aquifer formations, located at more than 300 m deep, consisted of a
previous phase of compilation, analysis and synthesis of the existing information about the area, followed by a coordinated
combination of different speciality studies: geology, stratigraphy, structural analysis, hydrogeology, hydrochemistry, geophysics
and remote sensing. Geological studies included geological mapping, definition of stratigraphical units and facies and structural
analysis. The aim of the hydrogeology study was to define aquifer formations, recharge area, aquifer points inventory and
groundwater flow directions for the establishment of piezometric and water quality observation nets. Special techniques were
applied, like thermal infrared aerial images and the evaluation of submarine groundwater discharge by means of natural radium
isotopes. Hydrochemical techniques, including majority elements characterization and stable isotopes (18O, 2H and 3H) determination, allowed classifying hydrochemical facies and establishing a renewal pattern for water within the system.
Geophysics was useful in determining the aquifer geometry, the features of the basement and the petrophysical characteristics
of the geological formations. Preliminary results show an important tectonic complexity and the possibilities for groundwater
uses in the area of study. 相似文献
40.
滑坡体三维地质建模与可视化分析 总被引:1,自引:0,他引:1
针对滑坡地质研究的自身特点,提出了面向滑坡地质体三维建模的NURBS-BRep混合数据结构和地质结构单元实体构造技术.通过对滑坡基础地质数据的预处理、滑坡数字地形和滑动面的三维建模、地质结构面的系统构造、地质结构体的生成和显示,形成了一套完整的滑坡三维地质模型的构建方法.将该方法应用于某水库滑坡,建立了相应的三维滑坡地质模型,并基于此模型进行了三维剖切分析、数字钻孔、等值线生成、滑块自动剖分、滑坡失稳可视化动态模拟和滑坡体方量精确计算等一系列实用的可视化分析,为滑坡稳定性的准确计算和客观评价提供了有力的支持. 相似文献