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971.
The aim of this paper is to evaluate the role of groundwater and sea weathering on the strength of the chalk rocks exposed on the coastline of the English Channel in Normandy, NW France. We present a study of the rock strength variations of three representative chalk units (Lewes Chalk, Seaford Chalk and Newhaven Chalk) exposed at various locations on the coastal chalk cliffs. The combination of UCS tests and SEM observations have been used (1) on dry natural chalk samples, (2) on chalk samples at various moisture contents, (3) on dry chalk samples submitted to a 10-day cycle of alternating wetting and drying by distilled water and by sea water. Dry chalk samples show low UCS strength (3.46–4 MPa) indicative of very weak rocks. When chalk samples are submitted to progressive water wetting, they present a decrease of UCS strength and Young's modulus of 40% to 50%. This behaviour begins at low values of water content within the chalk, i.e., for a degree of water saturation ranging between 10% and 17%. When chalk samples are submitted to an artificial weathering cycle with distilled water, a decrease in strength is observed, whereas the Young's modulus increases. SEM observations indicate the occurrence of microcracks and particle aggregates in the sample. When chalk samples are submitted to an artificial weathering with sea water, the decrease of UCS strength and Young's modulus achieves a minimum. SEM observations indicate salt crystals within the chalk. On the coastal cliffs of NW France, weathering processes depend both on chalk lithology, which show a range of sensitivity to weathering and on the location of the chalk in the coastal area. Processes allied to the degree of weathering (e.g., salt crystallisation or fresh water disaggregation) differ in the chalk massif, on the cliff face and on the shore platform.  相似文献   
972.
Neutron powder diffraction studies of calcite on heating towards the orientational order–disorder phase transition show that the phase transition is not a simple analogue of an Ising-like transition, but more similar to a rotational analogue of Lindemann melting. The transition is precipitated by the librational amplitude of the carbonate molecular ions exceeding a critical value rather than a result of a statistical entropy of ‘wrong’ orientations. Using tested interatomic potentials the single-particle orientational potential and nearest-neighbour orientational interactions have been calculated.  相似文献   
973.
A dense grid of multichannel high-resolution seismic sections from the Bay of Kiel in the western Baltic Sea has been interpreted in order to reveal the Mesozoic and Cenozoic geological evolution of the northern part of the North German Basin. The overall geological evolution of the study area can be separated into four distinct periods. During the Triassic and the Early Jurassic, E–W extension and the deposition of clastic sediments initiated the movement of the underlying Zechstein evaporites. The deposition ceased during the Middle Jurassic, when the entire area was uplifted as a result of the Mid North Sea Doming. The uplift resulted in a pronounced erosion of Upper Triassic and Lower Jurassic strata. This event is marked by a clear angular unconformity on all the seismic sections. The region remained an area of non-deposition until the end of the Early Cretaceous, when the sedimentation resumed in the area. Throughout the Late Cretaceous the sedimentation took place under tectonic quiescence. Reactivated salt movement is observed at the Cretaceous Cenozoic transition as a result of the change from an extensional to compressional regional stress field. The vertical salt movement influenced the Cenozoic sedimentation and resulted in thin-skinned faulting.  相似文献   
974.
Mineral exploration drillholes and geoelectric prospecting provide for the first time evidence for thrusting of the South Carpathian Paleozoic basement over northerly adjacent Middle Miocene sediments. Investigations were carried out in two locations, 30 km apart, along the northern margin of the Poiana Rusca Mountains, Romania, southwestern Carpathians. Drill holes in both locations encountered weakly consolidated Middle Miocene clay, sand, and fine gravel below Paleozoic low-grade metamorphic rocks. Intersections from various drill holes demonstrate the presence of low-angle thrusting. Kinematic indicators are so far lacking, but with a thrust direction oriented roughly normal to strike of the Poiana Rusca Mountains, minimum displacement is 1–1.4 km in northwestern or northern direction, respectively. Thrusting occurred most likely during the Late Miocene–Pliocene, whereafter Quaternary regional uplift dissected the thrust plane. In the tectonic framework of Neogene dextral translation of the Tisza–Dacia Block against the southerly adjacent Moesian Platform, transtension appears responsible for Middle Miocene basin formation along the northern margin of the Poiana Rusca region. Proceeding collision of the Tisza–Dacia Block with the East European Craton introduced stronger impingement of the Tisza–Dacia Block against the Moesian Platform, leading to a Late Miocene–Pliocene transpressional regime, in which the northern Poiana Rusca basement was thrust over its adjacent Middle Miocene sediments.  相似文献   
975.
Calcium isotope fractionation in calcite and aragonite   总被引:1,自引:0,他引:1  
Calcium isotope fractionation was measured on skeletal aragonite and calcite from different marine biota and on inorganic calcite. Precipitation temperatures ranged from 0 to 28°C. Calcium isotope fractionation shows a temperature dependence in accordance with previous observations: 1000 · ln(αcc) = −1.4 + 0.021 · T (°C) for calcite and 1000 · ln(αar) = −1.9 + 0.017 · T (°C) for aragonite. Within uncertainty the temperature slopes are identical for the two polymorphs. However, at all temperatures calcium isotopes are more fractionated in aragonite than in calcite. The offset in δ44/40Ca is about 0.6‰. The underlying mechanism for this offset may be related to the different coordination numbers and bond strengths of the calcium ions in calcite and aragonite crystals, or to different Ca reaction behavior at the solid-liquid interface. Recently, the observed temperature dependence of the Ca isotope fractionation was explained quantitatively by the temperature control on precipitation rates of calcium carbonates in an experimental setting (Lemarchand et al., 2004). We show that this mechanism can in principle also be applied to CaCO3 precipitation in natural environments in normal marine settings. Following this model, Ca isotope fractionation in marine Ca carbonates is primarily controlled by precipitation rates. On the other hand the larger Ca isotope fractionation of aragonite compared to calcite can not be explained by different precipitation rates. The rate control model of Ca isotope fractionation predicts a strong dependence of the Ca isotopic composition of carbonates on ambient CO32− concentration. While this model is in general accordance with our observations in marine carbonates, cultured specimens of the planktic foraminifer Orbulina universa show no dependence of Ca-isotope fractionation on the ambient CO32− concentration. The latter observation implies that the carbonate chemistry in the calcifying vesicles of the foraminifer is independent from the ambient carbonate ion concentration of the surrounding water.  相似文献   
976.
977.
978.
979.
Growth of zircon with respect to that of garnet has been studied using a combination of petrography, U–Pb dating and oxygen isotope analysis. The aim is to document the mechanism and pressure–temperature conditions of zircon growth during metamorphism in order to better constrain the Tertiary metamorphic history of Naxos, Greece. Two metamorphisms are recognised: (1) an Eocene Franciscan metamorphism (M1) and (2) a widespread Miocene Barrovian metamorphism (M2) that increases from greenschist facies up to partial melting. An amphibolite sample contains zircon crystals characterised by a magmatic core and two metamorphic rims, denoted as A and B, dated at 200–270, 42–69, and 14–19 Ma, respectively. The first metamorphic rim A (δ18O = 7 ± 1‰) preserves the δ18O value of the magmatic core (6.2 ± 0.8‰), whereas rim B is characterised by higher δ18O values (7.8 ± 1.8‰). These observations indicate the formation of A rims by solid-state recrystallisation in a closed system with regard to oxygen and those of B in an open system. Compositional zoning in garnet is interpreted as the result of decompressional heating. Zircon B rims and garnet rims display similar δ18O values which indicates a contemporaneous growth of garnet and zircon rims during the Miocene Barrovian event (M2). Calcic gneiss and metapelite samples contain zircon crystals with single metamorphic overgrowths aged 41–57 Ma. δ18O values measured in zircon overgrowths (11.8 ± 1.4‰) from the calcic gneiss are similar to those measured in garnet rims (11.4 ± 1.1‰) from the same rock. This suggests that garnet rims and zircon overgrowths grew during the high pressure–low temperature event in equilibrium with prograde fluids. In the metapelite sample, δ18O values are similar in garnet cores (14.8 ± 0.2‰) and in zircon metamorphic overgrowths (14.2 ± 0.5‰). As zircon overgrowths have been dated at ca. 50 Ma by U–Pb, garnet cores and zircon overgrowths are interpreted to have grown during the high pressure event.

As demonstrated here for the island of Naxos, correlating the crystallisation of zircon with that of metamorphic index minerals such as garnet using stable isotope composition and U–Pb determination is a powerful tool for deciphering the mechanism of zircon growth and pin-pointing zircon crystallisation within the metamorphic history of a terrain. This approach is potentially hampered by an inability to verify the degree of textural equilibrium of zircon with other mineral phases, and the possible preservation (in metamorphic rims) of isotopic signatures from pre-existing zircon when they form by recrystallisation. Nevertheless, this study illustrates the application of this approach in providing key constraints on the timing and mechanism of growth of minerals important to understanding metamorphic petrogenesis.  相似文献   

980.
Quantum mechanical calculations based on the density functional theory (DFT) are used to study the crystal structures of dioctahedral 2:1 phyllosilicates. The isomorphous cation substitution is investigated by exploring different substitutions of octahedral Al3+ by Mg2+ or Fe3+, tetrahedral substitution of Si4+ by Al3+, and different interlayer cations (IC) (Na+, K+, Ca2+, and Mg2+). Samples with different kinds of layer charges are studied: only tetrahedrally charged, only octahedrally charged, or mixed octahedral/tetrahedral charged. The effect of the relative arrangements of these substitutions on the lattice parameters and total energy is studied. The experimental observation of segregation tendency of Fe3+ and dispersion tendency of Mg2+ in the octahedral sheet is reproduced and explained with reference to the relative energies of the octahedral cation arrangements. These energies are higher than those due to the IC/tetrahedral and IC/octahedral relative arrangements. The tetrahedral and octahedral substitutions that generate charged layers also tend to be dispersed. The octahedral cation exchange potentials change with the IC-charge/ionic radius value.  相似文献   
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