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131.
中国东部古生界沉积—改造型铁矿床含矿岩系基本上由细碎屑—碳酸盐岩组成,而且常与富铁白云岩共生。矿体产状多与围岩一致,呈沉积整合接触。矿床中普遍发育有后生“再造”型矿体,呈脉状叠加在层状矿体之上,有明显的穿层现象。 海解作用是沉积成矿的重要因素,再造成矿作用是在沉积富铁碳酸盐建造的基础上发生富铁碳酸盐矿物的重溶,铁质被搬运、迁移,最后在碱性或偏碱性围岩中重新沉淀出来。 相似文献
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A global-scale glaciation occurred at about 600 Ma ago. As a result, the Earth became the “Snowball Earth“. The glaciation came to the end abruptly when atmospheric carbon dioxide increased to such an extent as to be about 350 times the modem level because of subaerial volcanic degassing. The rapid termination of glaciation would have led to warming of the Snowball Earth and extreme greenhouse conditions would have been created. The transfer of atmospheric carbon dioxide to oceans would give rise to the rapid precipitation of calcium carbonate in warm surface seawaters, thus forming the cap carbonate rocks as observed worldwide today. Regionally persisting, thin layers of carbonate rocks directly and ubiquitously overlie Proterozoic glacial deposits almost on every continent, and are commonly referred to as cap carbonates. Their unusual litho- fabrics, stratigraphically abrupt basal and upper-level contacts and strongly negative carbonate isotopic signatures ( δ ^13Cearb. values range from -7.0‰ —0‰) suggest a chemical oceanographic origin, the details of which remain unknown. It is proposed that these enigmatic deposits are related to the destabilization of gaseous hydrate in terrestrial permafrost following rapid postglacial warming and flooding of widely exposed continental shelves and internal basins. The authors carried out studies on the geochemistry, sedimentology and palacontology of the Sinian cap carbonates in Guizhou and Hunan provinces, including the occurrence of cap carbonates of unusual fabrics, strongly negative carbon isotopic signatures, and a lot of bitumen nodules.From the results it is suggested that the cap carbonates were formed from solid methane seepage, and it is in agreement with Kennedy‘‘ s viewpoint (2001) that the cap carbonates resulted from the rapid precipitation of calcium carbonate in response to solid methane seepage. 相似文献
134.
In terms of major element, trace element and REE geochemical characteristics ofvolcanic rocks in the area studied and by making use of the TiO2-K2O-P2O5,The-Hf-Ta and Zr-Nb-Y trianglar diagrams and the environmental discrimination diagrams of incompatible ele-ment distribution pattems,the authors have drawn some conclusions that are different from those by previous workers.It is concluded that volcanic rocks in the Laochang Ag polymetallic deposit at Lancang,Yunnan belong to continental within-plate alkali basalts, and that their geotectonic setting seems to be at the northeastern margin of East Gondwana Land. 相似文献
135.
廖卫华 《中国科学D辑(英文版)》2002,45(4):380-384
The Frasnian-Famennian (F-F) mass extinction is one of the five great extinctions of marine life during the Phanerozoic. The
F-F event killed most of the Devonian reefs, the characteristic Devonian corals, stromatoporoids, bryozoans, nearly all tentaculites,
a few superfamilies of brachiopods, such as Atrypacea and Pentameracea and some important elements of goniatites, such as
Manticoceras.
The end-Frasnian was a phase of mass extinction. A large number of shelly benthos were killed by the F-F event. Early and
middle Famennian was the survival interval. The marine faunas were very rare at that time. The late Famennian was the recovery
interval. There appeared to have many new taxa in the Strunian stage. It lacked a radiation interval in Late Devonian Famennian
because another event (the D-C mass extinction) happened at the Devonian-Carboniferous boundary.
Several causes for the F-F mass extinction have been proposed by some geologists, which have been grouped into two broad types,
terrestrial and extraterrestrial. The former is related to sea level changes, climate changes and anoxic water event. The
latter is linked with some forms of meteorite impact.
A large-scale eustatic change of sea level and black shales representing an anoxic environment has been invoked to explain
one of the causes for the F-F mass extinction. 相似文献
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一种土的非线性弹性本构模型参数的反演方法 总被引:2,自引:1,他引:1
旨在提出一种土的非线性弹性本构模型参数反演的方法。以现今普遍实行的地基载荷试验为基础,依据遗传算法的组合优化理论,采用正演计算和遗传算法优化相结合的方式,建立了土层非线性弹性本构模型参数反演的方法;并依据某黄土场地地基载荷试验数据,实施了黄土土层非线性弹性本构模型参数反演的全过程。计算结果表明,所建立的方法可以实现土层非线性弹性本构模型中相互关联的多个参数的组合优化,并在对初始值要求较低的情况下,可以获得良好的参数反演精度。从而为土的变形特性分析和土与其中及相邻结构的共同作用分析,提供了较好的土体本构模型参数的确定方法。 相似文献
138.
The speciation and thermodynamic properties of ferric chloride complexes in hydrothermal solutions and hypersaline brines are still poorly understood, despite the importance of this element as a micronutrient and ore-component. Available experimental data are limited to room temperature and relatively low chloride concentrations. This paper reports results of UV-Vis spectrophotometric and synchrotron XAFS experiments of ferric chloride complexes in chloride concentrations up to 15 m and at temperatures of 25-90 °C. Qualitative interpretation of the UV-Vis spectra shows that FeCl2+, FeCl2+, FeCl3(aq) and FeCl4− were present in the experimental solutions. As chloride concentrations increase, higher ligand number complexes become important with FeCl4− predominating in solutions containing more than 10 m at 25 °C. The predominance fields of FeCl3(aq) and FeCl4− expand to lower Cl concentrations with increasing T. Both XANES and UV-Vis spectra reveal a major change in the geometry of the complex between FeCl2+ and FeCl3(aq). EXAFS data confirm that the number of chloride ligands increases with increasing chloride concentration and show that Fe3+, FeCl2+ and FeCl2+ share an octahedral geometry. FeCl3(aq) could be either tetrahedral or trigonal dipyramidal, while FeCl4− is expected to be tetrahedral. EXAFS data support a tetrahedral geometry for FeCl4−, especially at 90 °C, but do not allow to distinguish between a tetrahedral or trigonal dipyramidal geometry for FeCl3(aq) because of similar Fe-Cl distances. At room temperature, EXAFS data suggest that FeCl3(aq) may be a mixture of octahedral and tetrahedral or trigonal dipyramidal forms.The room temperature formation constants for three ferric chloride complexes (FeCl2+, FeCl3(aq) and FeCl4−) determined from the UV data are generally in good agreement with previous studies. Calculations based on the properties extrapolated to 300 °C show that hematite solubility is much higher than previously estimated, and that the high orders complexes FeCl3(aq) and FeCl4− are important at high temperatures even in solutions with low chloride concentrations. The accuracy of these properties is limited by a poor understanding of activity-composition relationships in concentrated electrolytes, and by limitations in the available experimental techniques and extrapolation algorithms; however, the inclusion of higher order complexes in numerical models of ore transport and deposition allows for a more accurate qualitative prediction of Fe behaviour in hydrothermal and hypersaline systems. 相似文献
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