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在某些地球化学环境中,微生物对水─岩相互作用有重要影响。本文通过氧化亚铁硫杆菌与硫化物相互作用试验,初步研究了氧化亚铁硫杆菌作用引起水─岩介质变化特征,分析了氧化亚铁硫杆菌水文地球化学作用的一些规律。 相似文献
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对我国南方中新生代地洼盆地中的砂岩铜矿床进行了化学动力学与热力学的理论与实验研究。矿源岩中以辉铜矿和黄铜矿最有利于溶解和迁移,NaCl对Cu的溶解和含矿流体的形成起了催化作用。溶液中Cu以络合物的形式迁移,其中以一价铜氯络合物为主;温度的降低和溶液中性化导致了络合物的失稳、分解和铜矿物的沉淀。铜矿物的化学动力学和热力学制约了砂岩铜矿中以辉铜矿为主及矿床分带的形成。 相似文献
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本文对Ni40Mn30Fe30合金与在不同焙烧温度下得到的含水叶蜡,在高温超高压下的反应进行了实验研究,温度测至1420℃,压是至5.5GPa,研究了该反应的物质-化学机制,以及反应速率与温度,压力,含水量等参数的关系,对高压下物质迁移运动的固有特征进行了探讨。 相似文献
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This paper presents a method of establishing a hydrothermal ore-forming reaction system.On the basis of the study of four typical hydrothermal deposits,the following conclusions concerning geochemical dynamic controlling during hydrothermal mineralization have been sions concerning geochemical dynaamic controlling during hydrothermal mineralization have been drawn:(1)The regional tectonic activities control the concentration and dispersion of elements in the ore-forming process in terms of their effects on the thermodynamic nature and conditions of the ore-forming reaction system.(2)During hydrothermal mineralization the activites of ore-bearing faults can be divideb into two stages:the brittle splitting stage and the brittle-tough tensing stage,which would create characteristically different geodynamic conditions for the geochemical thermodynamic ore-forming system.(3)The hydrothermal ore-forming reaaction system is an open dynamic system.At the brittle splitting stage the system was so strongly supersaturated and unequilibrated as to speed up and enhance the crystallization and differentiation of ore-forming fluids.And at the brittle-tough tensing stage,the ore-forming system was in a weak supersaturated state;with decreasing temperature and pressure the crystallization of oreforming material would show down,and it can be regarded as an equilibrated state.(4)In the lates stages of hydrothermal evolution,gold would be concentrated in the residual ore-forming solution.The pulsating fracture activite in this stage led to the crush of pyrite ore and it was then filled with gold-enriched solution,forming high-grage“fissure”gold ore.This ore-forming process could be called the coupling mechanism of ore formation. 相似文献
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通过对碳酸锰氧化实验的结果分析和讨论,建立了一种适合于锰氧化过程的非平衡热力学模型,并利用此模型对硫酸锰氧化过程作了热力学可行性分析,研究结果表明,碳酸锰氧化过程是矿物组合的变化过程,也是锰自身价态的转为过程,整个过程既存在平衡状态,又存在非平衡状态,是一个不可逆的,多相的复杂反应。 相似文献
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Zhang Sheng Li Tongjin Wang LiankuiGuangzhou Institute of Geochemistry Chinese Academy of SciencesWushan Guangzhou 《《地质学报》英文版》1997,71(4):433-445
The Changkeng gold-silver deposits consist of a sediment-hosted, disseminated gold deposit and a replacement-type silver deposit. The mineralizations of gold and silver are zoned and closely related to the silicification of carbonate and clastic rocks, so that siliceous ores dominate in the deposit. The mineralizing temperature ranges mainly from 300 to 170℃, and K+, Na+, Ca2+, Mg2+, and Cl- are the major ions in the ore-forming fluid. Calculations of distribution of metal complexes show that gold is mainly transported by hydrosulphide complexes, but chloride complexes of silver, iron, lead, and zinc, which are transformed into hydroxyl and hydrosulphide complexes under neutral to weak-alkaline circumstances in the late stage, predominate in the ore-forming solutions. Water-rock interaction is confirmed to be the effective mechanism for the formation of silver ores by computer modelling of reaction of hydrothermal solution with carbonate rocks. The solubility analyses demonstrate that the precipitation 相似文献
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Ralph Lehmann 《Journal of Atmospheric Chemistry》2004,47(1):45-78
When the output of a complex chemical model is analysed, a typical topic isthe determination of pathways, i.e., reaction sequences, that produce ordestroy a chemical species of interest.A representative example is the investigation of catalytic ozone destruction cycles in the stratosphere.An algorithm for the automatic determination of pathways in any given reactionsystem is presented. Under the assumption that reaction rates are known, it finds all significant pathways, i.e., all pathways with a rate above a prescribed threshold.The algorithm forms pathways step by step, starting from single reactions.The chemical species in the system are consecutively considered as `branching points'.For every branching-point species, each pathway producing it is connected witheach pathway consuming it.Rates proportional to `branching probabilities' are calculated.Pathways with a rate that is smaller than a prescribed threshold arediscarded.If a newly formed pathway contains sub-pathways, e.g., null cycles, it is split into these simpler pathways.In order to demonstrate the performance of the algorithm, it has been applied to the determination of catalytic ozone destruction cycles and methaneoxidation pathways in the stratosphere. 相似文献
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