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81.
总结不对称抽道集共反射面元叠加方法的工作经验,提出自由观测面自由反射界面不对称抽道集共反射面元叠加方法的处理思路和计算方法。在自由观测面的条件下,反射界面可分为简单倾斜平面、规则曲面和自由反射界面三种情况,针对不同情况讨论共反射面元的叠加方法。综合一般情况下的共反射面元叠加方法,提出了“鳞片法”的处理思路。 相似文献
82.
大别山南坡蕲春等地榴辉岩的发现及相关问题 总被引:1,自引:0,他引:1
20世纪90年代早、中期,一些研究者根据榴辉岩的出露情况,将大别山腹地的大别杂岩出露区划分为“北大别地体”、“UHP地体”和“宿松地体”3个不同性质的大地构造单元,其中“北大别地体”和“宿松地体”2个地体被视为不含榴辉岩的构造单元。然而,自90年代后期以来,在“北大别地体”中陆续发现了大量的榴辉岩露头。近期笔者在“宿松地体”中也首次发现了榴辉岩露头。上述事实表明前人仅仅根据榴辉岩的出露将大别杂岩划分为3个构造单元的认识是不妥的,大别杂岩应该为一个具有一定成因联系的构造-岩石单元,属于同一个大地构造单元。 相似文献
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86.
建立了用单道扫描电感耦合等离子体发射光谱法测定珊瑚礁中主量和微量元素的方法。珊瑚礁样品经酸溶解后,直接进行Ca、Mg、K、Na、V、Sr、Ba、Co、Ni、Pb、Li、Rb的测定,方法检出限为0.0004~0.1mg/L,精密度RSD<5%(n=6),样品的加标回收率为97%~105%。测定w(CaO)为50%的样品,结果与传统的EDTA容量法相符。方法经碳酸盐岩石国家一级标准物质验证可行,已用于大批量的珊瑚礁样品的测定。 相似文献
87.
底质不连续面是沉积作用中断时所形成的一种地层界面。根据底质的粘结程度可将底质不连续面划分为两大类:固底不连续面和硬底不连续面。固底不连续面中的简单停积面依靠沉积序列的变化来识别,界面上、下的生物地层带是连续的;而复成停积面上、下的生物地层带不连续。在硬底不连续面中,硬底的上、下地层属于同一个沉积体系,而继承性岩底的上、下地层则属于不同的沉积体系,其间发生过重大的沉积间断。根据底质控制的Glossifungites遗迹相和Trypanites遗迹相可以有效地识别各类不连续面并解释其成因。三种类型的不连续面具有层序地层学意义:①侵蚀性不连续面,包括低水位侵蚀面(LSE)和海进侵蚀面(TSE);②无沉积间断面;③沉积性不连续面(凝缩段)。 相似文献
88.
A method, based on the Hilbert–Huang spectral analysis, has been proposed by the authors to identify linear structures in which normal modes exist (i.e., real eigenvalues and eigenvectors). Frequently, all the eigenvalues and eigenvectors of linear structures are complex. In this paper, the method is extended further to identify general linear structures with complex modes using the free vibration response data polluted by noise. Measured response signals are first decomposed into modal responses using the method of Empirical Mode Decomposition with intermittency criteria. Each modal response contains the contribution of a complex conjugate pair of modes with a unique frequency and a damping ratio. Then, each modal response is decomposed in the frequency–time domain to yield instantaneous phase angle and amplitude using the Hilbert transform. Based on a single measurement of the impulse response time history at one appropriate location, the complex eigenvalues of the linear structure can be identified using a simple analysis procedure. When the response time histories are measured at all locations, the proposed methodology is capable of identifying the complex mode shapes as well as the mass, damping and stiffness matrices of the structure. The effectiveness and accuracy of the method presented are illustrated through numerical simulations. It is demonstrated that dynamic characteristics of linear structures with complex modes can be identified effectively using the proposed method. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
89.
Laser Ablation ICP-MS Analysis of Geological Materials Prepared as Lithium Borate Glasses 总被引:9,自引:0,他引:9
Stephen M. Eggins 《Geostandards and Geoanalytical Research》2003,27(2):147-162
A simple, rapid and precise method is described for determining trace elements by laser ablation (LA)-ICP-MS analysis in bulk geological materials that have been prepared as lithium borate glasses following standard procedures for XRF analysis. This approach reliably achieves complete sample digestion and provides for complementary XRF and LA-ICP-MS analysis of a full suite of major and trace elements from a single sample preparation. Highly precise analysis is enabled by rastering an ArF excimer laser (λ= 193nm) across fused samples to deliver a constant sample yield to the mass spectrometer without inter-element fractionation effects during each analysis. Capabilities of the method are demonstrated by determination of twenty five trace elements (Sc, Ti, V, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, REE, Hf, Ta, Pb, Th and U) in a diverse range of geological reference materials that includes peridotites, basalts, granites, metamorphic rocks and sediments. More than 90% of determinations are indistinguishable from published reference values at the 95% confidence level. Systematic bias greater than 5% is observed for only a handful of elements (Zr, Nb and U) and may be attributed in part to inaccurate calibration values used for the NIST SRM 612 glass in the case of Zr and Nb. Detection limits for several elements, most notably La, are compromised at ultra-trace levels by impurities in the lithium borate flux but can be corrected for by subtracting appropriate procedural blanks. Reliable Pb analysis has proved problematic due to variable degrees of contamination introduced during sample polishing prior to analysis and from Pt-crucibles previously used to fuse Pb-rich samples. Scope exists for extending the method to include internal standard element/isotope spiking, particularly where integrated XRF analysis is not available to characterise major and trace elements in the fused lithium borate glasses prior to LA-ICP-MS analysis. 相似文献
90.
William J. Chazey III Clive R. Neal Jinesh C. Jain William S. Kinman 《Geostandards and Geoanalytical Research》2003,27(2):181-192
The geochemical reference material BHVO-1 was analysed by a variety of techniques over a six year period. These techniques included inductively coupled plasma-mass spectrometry and atomic emission spectroscopy (ICP-MS and ICP-AES, respectively), laser ablation ICP-MS and spark source mass spectroscopy. Inconsistencies between the published consensus values reported by Gladney and Roelandts (1988, Geostandards Newsletter) and the results of our study are noted for Rb, Y, Zr, Pb and Th. The values reported here for Rb, Y, Zr and Pb are generally lower, while Th is higher than the consensus value. This is not an analytical artefact unique to the University of Notre Dame ICP-MS facility, as most of the BHVO-1 analyses reported over the last ten to twenty years are in agreement with our results. We propose new consensus values for each of these elements as follows: Rb = 9.3 ± 0.2 μg g-1 (compared to 11 ± 2 μg g-1), Y = 24.4 ± 1.3 μg g-1 (compared to 27.6 ± 1.7 μg g-1), Zr = 172 ± 10 μg g-1 (compared to 179 ± 21 μg g-1), Pb = 2.2 ± 0.2 μg g-1 (compared to 2.6 ± 0.9 μg g-1) and Th = 1.22 ± 0.02 μg g-1 (compared to 1.08 ± 0.15 μg g-1). 相似文献