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201.
202.
Aimed at the initial value problem of the particular second-order ordinary differential equations,y
=f(x, y), the symmetric methods (Quinlan and Tremaine, 1990) and our methods (Xu and Zhang, 1994) have been compared in detail by integrating the artificial earth satellite orbits in this paper. In the end, we point out clearly that the integral accuracy of numerical integration of the satellite orbits by applying our methods is obviously higher than that by applying the same order formula of the symmetric methods when the integration time-interval is not greater than 12000 periods. 相似文献
203.
204.
许康生 《地震地磁观测与研究》1992,13(2):15-19
地震泼由多种频率成份组成,在其传播过程中。由于地球介质的滤波作用,随着传播距离的增大。高频成份逐渐被衰减。周期越大的成份传播越远。因此,在地震观测上,不同频带的地震仪用于观测不同震中距范围的地震,使仪器较好地响应,就我国台网而言,短周期仪用于地方震、近震的监测,中长周期仪和长周期仪用于远震,极远震的监测,其中长周期仪偏重于记录极远震。但作者在实际分析工作中注意到,短周期仪的记录应用于远震,极远震的分析,显示出独特的作用,充分挖掘和利用短仪资料,将会更加丰富远震、极远震的震相资料。本文以高台地震台的资料为依据,从震中距和震级角度,与中长仪和长仪作比较,对短仪记录远震、极远震的震相及特征作了统计分析与初步探讨,并对新疆地区“影区”地震S波的记录、日本地区地震_PPcP等震相的出现提出了现象的存在,给出了相应的观测结果,以待步一步研究。 相似文献
205.
内蒙古正镶白旗碎斑熔岩岩石学特征及其岩相划分 总被引:4,自引:0,他引:4
白旗碎斑熔岩为不规则穹状体,可分为边缘玻质碎斑熔岩、过渡霏细碎斑熔岩、中心粒状碎斑熔岩和根部花岗斑岩四个岩性带。从玻质碎斑熔岩到粒状碎斑熔岩,斑晶碎裂度逐渐减弱,珠边结构在粒状碎斑熔岩中最发育,根部花岗斑岩与正常次火山岩相近。碎斑熔岩中钾长石有序度低,指示了岩石高温成因特征。白旌碎斑熔岩属太平洋岩系钙碱质系列,原始岩浆由来源于上地幔和下地壳熔体的混熔作用形成。 相似文献
206.
207.
208.
青藏高原腹地湖泊沉积对第四纪晚期古季风变化的响应 总被引:2,自引:0,他引:2
通过对青藏高原腹地的综合科学考察和对中心钻孔岩芯剖面的最新研究,用层序地层学与年代地层学和气候地层学相结合的方法,分辨出可可西里地区湖泊沉积记录(孔深7.25 m)的第四纪晚期距今3万余年以来的古气候变化,沉积物磁化率等因子综合表征的高原古季风变化是波动发展的,发生在仙女木期地质环境事件中的季风活动具有强烈暴发的特点,是高原季风发展中的突变事件,而且地表热点效应对其起到了激发作用。综合分析的研究成果表明,它的变化频谱与激变因子及其运行机制是伴随着青藏高原地质效应的演变而发展的,为研究第四纪冰消期以来的气候变化提供了新的信息。 相似文献
209.
Interaction between slab-derived melt and mantle peridotite and the role of slab melt as a metasomatizing agent in the sub-arc mantle is being increasingly recognized. Adakite, the slab melt erupted on the surface, usually exhibits anomalously high MgO, CaO, Cr and Ni contents that indicate interaction with mantle peridotitite. Here we note that Cenozoic adakites have Na2O contents below 5.8 wt.% with ∼95% samples lower than 5.0 wt.%, and are generally depleted in this component relative to experimental basalt partial melts (mostly beyond 5.0 wt.% and up to 9.0 wt.% Na2O) produced under 1.5-3.0 GPa conditions that are most relevant to adakite production. We interpret the adakite Na depletion to be also a consequence of the melt / rock reaction that takes place within the hot mantle wedge. During ascent and reaction with mantle peridotite, primary adakite melts gain mantle components MgO, CaO, Cr and Ni but lose Na2O, SiO2 and perhaps K2O to the mantle, leading to Na-rich mantle metasomatism. Selective assimilation of predominately mantle clinopyroxene, some spinel and minor olivine at high T/P has been considered to be an important process in producing high-Mg adakites from primary low-Mg slab melts [Killian, R., Stern, C. R., 2002. Constraints on the interaction between slab melts and the mantle wedge from adakitic glass in peridotite xenoliths. Eur. J. Mineral. 14, 25-36]. In such a process, Na depletion in the assimilated melt is the result of dilution due to the increase in melt mass. Phase relationships in the reaction system siliceous melt + peridotite and quantitative calculation suggest that assimilation of mantle clinopyroxene, olivine and spinel and fractional crystallization of sodic amphibole and orthopyroxene, under conditions of moderate T/P and increasing melt mass, is also an important process that modifies the composition of adakites and causes the Na depletion. 相似文献
210.
Xiang Xu 《Geochimica et cosmochimica acta》2006,70(17):4319-4331
Interaction of dissolved aqueous species with natural organic matter (NOM) is thought to be important in sequestering some species and enhancing the transport of others, but little is known about these interactions on a molecular scale. This paper describes a combined experimental 133Cs and 35Cl nuclear magnetic resonance (NMR) and computational molecular dynamics (MD) modeling study of the interaction of Cs+ and Cl− with Suwannee River NOM. The results provide a detailed picture of the molecular-scale structure and dynamics of these interactions. Individual NOM molecules are typically hundreds to thousands of Daltons in weight, and on the molecular scale their interaction with small dissolved species can be investigated in ways similar to those used to study the interaction of dissolved aqueous species with mineral surfaces. As for such surface interactions, understanding both the structural environments and the dynamics over a wide range of frequencies is essential. The NMR results show that Cs+ is associated with NOM at pH values from 3.4 ± 0.5 (unbuffered Suwannee River NOM solution) to 9.0 ± 0.5. The extent of interaction increases with decreasing CsCl concentration at constant pH. It also decreases with increasing pH at constant CsCl concentration due to pH-dependent negative structural charge development on the NOM caused by progressive deprotonation of carboxylic and phenolic groups. The presence of NOM has little effect on the 133Cs chemical shifts, demonstrating that its local coordination environment does not change significantly due to interaction with the NOM. Narrow, solution-like line widths indicate rapid exchange of Cs+ between the NOM and bulk solution at frequencies of >102 Hz. The MD simulations support these results and show that Cs+ is associated with the NOM principally as outer sphere complexes and that this interaction does not reduce the Cs+ diffusion coefficient sufficiently to cause NMR line broadening. The 35Cl NMR data and the MD results are consistent in demonstrating that there is no significant complexation between Cl− and NOM in the pH range investigated, consistent with negative structural charge on the NOM. 相似文献