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21.
Himalayan magmatism and porphyry copper–molybdenum mineralization in the Yulong ore belt, East Tibet
Summary ?The NW–SE-trending Yulong porphyry Cu–Mo ore belt, situated in the Sanjiang0 area of eastern Tibet, is approximately 400 km
long and 35 to 70 km wide. Complex tectonic and magmatic processes during the Himalayan epoch have given rise to favorable
conditions for porphyry-type Cu–Mo mineralization.
Porphyry masses of the Himalayan epoch in the Yulong ore belt are distributed in groups along regional NW–SE striking tectonic
lineaments. They were emplaced mainly into Triassic and Lower Permian sedimentary-volcanic rocks. K–Ar und U–Pb isotopic datings
give an intrusion age range of 57–26 Ma. The porphyries are mainly of biotite monzogranitic and biotite syenogranitic compositions.
Geological and geochemical data indicate that the various porphyritic intrusions in the belt had a common or similar magma
source, are metaluminous to peraluminous, Nb–Y–Ba-depleted, I-type granitoids, and belong to the high-K calc-alkaline series.
Within the Yulong subvolcanic belt a number of porphyry stocks bear typical porphyry type Cu–Mo alteration and mineralization.
The most prominent porphyry Co–Mo deposits include Yulong, Malasongduo, Duoxiasongduo, Mangzong and Zhanaga, of which Yulong
is one of the largest porphyry Cu (Mo) deposits in China with approximately 8 × 106 tons of contained Cu metal. Hydrothermal alteration at Yulong developed around a biotite–monzogranitic porphyry stock that
was emplaced within Upper Triassic limestone, siltstone and mudstone. The earliest alteration was due to the effects of contact
metamorphism of the country rocks and alkali metasomatism (potassic alteration) within and around the porphyry body. The alteration
of this stage was accompanied by a small amount of disseminated and veinlet Cu–Mo sulfide mineralization. Later alteration–mineralization
zones form more or less concentric shells around the potassic zone, around which are distributed a phyllic or quartz–sericite–pyrite
zone, a silicification and argillic zone, and a propylitic zone.
Fluid inclusion data indicate that three types of fluids were involved in the alteration–mineralization processes: (1) early
high temperature (660–420 °C) and high salinity (30–51 wt% NaCl equiv) fluids responsible for the potassic alteration and
the earliest disseminated and/or veinlet Cu–Mo sulfide mineralization; (2) intermediate unmixed fluids corresponding to phyllic
alteration and most Cu–Mo sulfide mineralization, with salinities of 30–50 wt% NaCl equiv and homogenization temperatures
of 460–280 °C; and (3) late low to moderate temperature (300–160 °C) and low salinity (6–13 wt% NaCl equiv) fluids responsible
for argillic and propylitic alteration. Hydrogen and oxygen isotopic studies show that the early hydrothermal fluids are of
magmatic origin and were succeeded by increasing amounts of meteoric-derived convective waters. Sulfur isotopes also indicate
a magmatic source for the sulfur in the early sulfide mineralization, with the increasing addition of sedimentary sulfur outward
from the porphyry stock.
Received August 29, 2001; revised version accepted May 1, 2002
Published online: November 29, 2002 相似文献
22.
利用三维有限元模拟两层地球模型(包括弹性层和粘弹性层)介质的横向不均匀和断层错动的复杂性对震后地表位移场的影响,其数值结果包括弹性解和粘弹性解。结果表明,震后位移场的分布特征不仅与粘弹性层的流变特性有关,还与弹性层介质的剪切模量以及断层的同震错动有关。 相似文献
23.
24.
介绍了一种新颖的静态传感器网络实现方法,它利用可移动的中继节点来收集静态传感器网络的数据,有效的节约各传感器节点的能源,延长整个传感器网络的有效工作时间。也可以对该方法进行适当的改进,应用到某些实时性要求较高的场合中去。然后介绍了应用该原理实现的一个通讯协议。 相似文献
25.
26.
近年我国区域水文研究的若干进展 总被引:1,自引:1,他引:0
我国区域水文学的研究是在解放后其正发展起来的。尽管迄今人们对区域水文学仍有不同的认识,例如区域水文学是否可以与水文地理学等同,或是区域水文学是否应隶属于区域地理学等等,但是作为水文学的分支学科是无疑的。区域水文学从整体的观点来研究区域水文情势。区城可以是功能区,如城市、出口加工中心区等,或为自然景观区,如干旱区、喀斯特区等,也可以是行政区。目前,许多水文水利工作者已在致力于区域水文学的研究。 相似文献
27.
28.
Recharge source and hydrogeochemical evolution of shallow groundwater in a complex alluvial fan system,southwest of North China Plain 总被引:4,自引:0,他引:4
Fadong Li Guoying Pan Changyuan Tang Qiuying Zhang Jingjie Yu 《Environmental Geology》2008,55(5):1109-1122
Many cities around the world are developed at alluvial fans. With economic and industrial development and increase in population,
quality and quantity of groundwater are often damaged by over-exploitation in these areas. In order to realistically assess
these groundwater resources and their sustainability, it is vital to understand the recharge sources and hydrogeochemical
evolution of groundwater in alluvial fans. In March 2006, groundwater and surface water were sampled for major element analysis
and stable isotope (oxygen-18 and deuterium) compositions in Xinxiang, which is located at a complex alluvial fan system composed
of a mountainous area, Taihang Mt. alluvial fan and Yellow River alluvial fan. In the Taihang mountainous area, the groundwater
was recharged by precipitation and was characterized by Ca–HCO3 type water with depleted δ18O and δD (mean value of −8.8‰ δ18O). Along the flow path from the mountainous area to Taihang Mt. alluvial fan, the groundwater became geochemically complex
(Ca–Na–Mg–HCO3–Cl–SO4 type), and heavier δ18O and δD were observed (around −8‰ δ18O). Before the surface water with mean δ18O of −8.7‰ recharged to groundwater, it underwent isotopic enrichment in Taihang Mt. alluvial fan. Chemical mixture and ion
exchange are expected to be responsible for the chemical evolution of groundwater in Yellow River alluvial fan. Transferred
water from the Yellow River is the main source of the groundwater in the Yellow River alluvial fan in the south of the study
area, and stable isotopic compositions of the groundwater (mean value of −8.8‰ δ18O) were similar to those of transferred water (−8.9‰), increasing from the southern boundary of the study area to the distal
end of the fan. The groundwater underwent chemical evolution from Ca–HCO3, Na–HCO3, to Na–SO4. A conceptual model, integrating stiff diagrams, is used to describe the spatial variation of recharge sources, chemical
evolution, and groundwater flow paths in the complex alluvial fan aquifer system. 相似文献
29.
Mauro Lo Cascio Yan Liang Nobumichi Shimizu Paul C. Hess 《Contributions to Mineralogy and Petrology》2008,156(1):87-102
The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing
pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum
capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free,
olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across
the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations
in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and
is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange
between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt
interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is
especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt
partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive
boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume
diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements
in residual minerals reequilibrate with their surrounding melt.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
30.
Yan Liang 《Geochimica et cosmochimica acta》2008,72(15):3804-3821
Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle. 相似文献