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991.
The mafic dykes in Wadi Mandar-Wadi Um Adawi area are as follows: (1) calc-alkaline lamprophyre (i.e., kersantite and spessartite), (2) diabase, and (3) alkaline lamprophyre (i.e., camptonite). The field relations reveal that the emplacement of calc-alkaline lamprophyres preceded the diabase dykes, while alkaline lamprophyres emplaced later than the diabase dykes. Calc-alkaline are basaltic andesite, basaltic trachyandesite to basalt, while the diabase dykes and alkaline lamprophyres are basaltic in composition. These dykes are characterized by metaluminous character. Calc-alkaline lamprophyres and diabase dykes show transitional affinity from calc-alkaline to alkaline, while the alkaline lamprophyres exhibit more strong alkaline character. The mafic dykes were crystallized under temperature 1100–1150 °C and pressure 3–5 kbars in a high oxygen fugacity conditions. Fe-Ti oxides in the dykes are represented by ilmenite and Ti-magnetite. The chemistry of the sulfides hosted in those mafic dykes suggests a magmatic-hydrothermal origin for these minerals. The geochemical behavior of high field strength elements and large ion lithophile elements in these dykes excludes the derivation of diabase or alkaline lamprophyre either by partial melting or fractional crystallization from calc-alkaline lamprophyre. The parental magmatic sources of the studied dykes were generated from crustal material with addition of mantle-derived melt during the post-collisional stage. The mafic dykes in Wadi Mandar-Wadi Um Adawi area were generated from different magmatic sources by partial melting and subsequent fractional crystallization. In addition, the crustal contamination/assimilation process has a prominent role in the magmatic evolution of diabase and alkaline lamprophyre dykes.  相似文献   
992.
993.
The paper reviews data (acquired in 2007–2016) on aliphatic and polycyclic aromatic hydrocarbons in comparison with data on concentrations of lipids, Corg, and chlorophyll a in the water and bottom sediments the river–sea geochemical barrier (for the Northern Dvina, Ob, Yenisei, and Lena rivers). It was established that the concentrations of anthropogenic hydrocarbons decrease and these compounds precipitate like other organic compounds and particulate matter, where riverine and marine waters mix. Relatively pure water flows in the pelagic zones of seas. In spite of low temperatures in the Arctic, anthropogenic hydrocarbons transform so rapidly that natural compounds dominate in the water and bottom sediments: autochthonous in the seawater and allochthonous in the bottom sediments.  相似文献   
994.
995.
996.
Aplite dikes intruding the Proterozoic 1.42(±?3) Ga Longs Peak-St. Vrain Silver Plume-type peraluminous granite near Jamestown, Colorado, contain F, P, and rare earth element (REE)-rich globular segregations, with 40–46% REE, 3.7–4.8 wt% P2O5, and 5–8 wt% F. A combination of textural features and geochemical data suggest that the aplite and REE-rich globular segregations co-existed as two co-genetic liquids prior to their crystallization, and we propose that they are formed by silicate–fluoride?+?phosphate (+?S?+?CO2) melt immiscibility following ascent, cooling, and decompression of what was initially a single homogeneous magma that intruded the granite. The REE distribution coefficients between the silica-rich aplites and REE-rich segregations are in good agreement with experimentally determined distribution coefficients for immiscible silicate–fluoride?+?phosphate melts. Although monazite-(Ce) and uraninite U–Th–Pb microprobe ages for the segregations yield 1.420(±?25) and 1.442(±?8) Ga, respectively, thus suggesting a co-genetic relationship with their host granite, εNd1.42Ga values for the granites and related granitic pegmatites range from ??3.3 to ??4.7 (average ??3.9), and differ from the values for both the aplites and REE-rich segregations, which range from ??1.0 to ??2.2 (average ??1.6). Furthermore, the granites and pegmatites have (La/Yb)N <50 with significant negative Eu anomalies, which contrast with higher (La/Yb)N >100 and absence of an Eu anomaly in both the aplites and segregations. These data are consistent with the aplite dikes and the REE-rich segregations they contain being co-genetic, but derived from a source different from that of the granite. The higher εNd1.42Ga values for the aplites and REE-rich segregations suggest that the magma from which they separated had a more mafic and deeper, dryer and hotter source in the lower crust or upper mantle compared to the quartzo-feldspathic upper crustal source proposed for the Longs Peak-St. Vrain granite.  相似文献   
997.
The Pozanti–Karsanti ophiolite (PKO) is one of the largest oceanic remnants in the Tauride belt, Turkey. Micro-diamonds were recovered from the podiform chromitites, and these diamonds were investigated based on morphology, color, cathodoluminescence, nitrogen content, carbon and nitrogen isotopes, internal structure and inclusions. The diamonds recovered from the PKO are mainly mixed-habit diamonds with sectors of different brightness under the cathodoluminescence images. The total δ13C range of the PKO diamonds varies between ??18.8 and ??28.4‰, with a principle δ13C mode at ??25‰. Nitrogen contents of the diamonds range from 7 to 541 ppm with a mean value of 171 ppm, and the δ15N values range from ??19.1 to 16.6‰, with a δ15N mode of ??9‰. Stacking faults and partial dislocations are commonly observed in the Transmission Electron Microscopy foils whereas inclusions are rather rare. Combinations of (Ca0.81Mn0.19)SiO3, NiMnCo-alloy and nano-sized, quenched fluid phases were observed as inclusions in the PKO diamonds. We believe that the 13C-depleted carbon signature of the PKO diamonds derived from previously subducted crustal matter. These diamonds may have crystallized from C-saturated fluids in the asthenospheric mantle at depth below 250 km which were subsequently carried rapidly upward by asthenospheric melts.  相似文献   
998.
Fluoro-sodalite was synthesized for the first time at temperatures of 400–800°C and H2O pressures of 1–2 kbar in the Si–Al–Na–H–O–F system. X-ray diffraction and infrared spectroscopic investigations showed that fluorine is incorporated in the sodalite structure as anionic octahedral groups, [AlF6]3–, the number of which can vary from 0 to 1. Correspondingly, the end-members of the F-sodalite series are Na7(H2O)8[Si5Al7O24] and Na8(AlF6)(H2O)4[Si7Al5O24]. Depending on the composition of the system, F-sodalite associates at 500–650°C with nepheline, albite, cryolite, and villiaumite, which are joined by analcime below 500°C and aluminosilicate melt above 650°C. Fluorine-bearing sulfate–chlorine-sodalite was found for the first time in a pegmatite sample from the Lovozero massif. The highest fraction of the fluorine end-member in natural sodalite is 0.2. The incorporation of F into the sodalite structure requires much more energy compared with Cl and SO 4 2- , because it is accompanied by a structural rearrangement and a transition from tetrahedral Al to octahedral Al.  相似文献   
999.
Garnet crystals with quartz inclusions were hydrothermally crystallized from oxide starting materials in piston–cylinder apparatuses at pressures from 0.5 to 3 GPa and temperatures ranging from 700 to 800 °C to study how entrapment conditions affect remnant pressures of quartz inclusions used for quartz-in-garnet (QuiG) elastic thermobarometry. Systematic changes of the 128, 206 and 464 cm?1 Raman band frequencies of quartz were used to determine pressures of quartz inclusions in garnet using Raman spectroscopy calibrations that describe the P–T dependencies of Raman band shifts for quartz under hydrostatic pressure. Within analytical uncertainties, inclusion pressures calculated for each of the three Raman band frequencies are equivalent, which suggests that non-hydrostatic stress effects caused by elastic anisotropy in quartz are smaller than measurement errors. The experimental quartz inclusions have pressures ranging from ??0.351 to 1.247 GPa that span the range of values observed for quartz inclusions in garnets from natural rocks. Quartz inclusion pressures were used to model P–T conditions at which the inclusions could have been trapped. The accuracy of QuiG thermobarometry was evaluated by considering the differences between pressures measured during experiments and pressures calculated using published equation of state parameters for quartz and garnet. Our experimental results demonstrate that Raman measurements performed at room temperature can be used without corrections to estimate garnet crystallization pressures. Calculated entrapment pressures for quartz inclusions in garnet are less than ~?10% different from pressures measured during the experiments. Because the method is simple to apply with reasonable accuracy, we expect widespread usage of QuiG thermobarometry to estimate crystallization conditions for garnet-bearing silicic rocks.  相似文献   
1000.
The geodynamic nature of the Late Neoproterozoic island-arc dacites (691 ± 8.8 Ma) and rift basalts (572 ± 6.5 Ma) of the Kiselikhinskaya Formation, Kutukasskaya Group, in the Isakovskii terrane is inferred from geochemical data and U–Pb zircon (SHRIMP-II) dates. The volcanic rocks were produced during the late evolutionary history of the Yenisei Range, starting at the origin of oceanic crustal fragments and their accretion to the Siberian craton to the postaccretionary crustal extension and the onset of the Caledonian orogenesis. The reproduced sequence of geological processes marks the early evolution of the Paleo- Asian Ocean in its junction zone with the Siberian craton. The data refine the composition and age of volcanic rocks in the trans-Angara part of the Yenisei Range and specifics of the Neoproterozoic evolution of the Sayan–Yenisei accretionary belt.  相似文献   
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