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41.
The Eagle Ford Shale of Central and South Texas is currently of great interest for oil and gas exploration and production. Laboratory studies show that the Eagle Ford Shale is anisotropic, with a correlation between anisotropy and total organic carbon. Organic materials are usually more compliant than other minerals present in organic‐rich shales, and their shapes and distribution are usually anisotropic. This makes organic materials an important source of anisotropy in organic‐rich shales. Neglecting shale anisotropy may lead to incorrect estimates of rock and fluid properties derived from inversion of amplitude versus offset seismic data. Organic materials have a significant effect on the PP and PS reflection amplitudes from the Austin Chalk/Upper Eagle Ford interface, the Upper Eagle Ford/Lower Eagle Ford interface, and the Lower Eagle Ford/Buda Limestone interface. The higher kerogen content of the Lower Eagle Ford compared with that of the Upper Eagle Ford leads to a negative PP reflection amplitude that dims with offset, whereas the PS reflection coefficient increases in magnitude with increasing offset. The PP and PS reflection coefficients at the Austin Chalk/Upper Eagle Ford interface, the Upper Eagle Ford/Lower Eagle Ford interface, and the Lower Eagle Ford/Buda Limestone interface all increase in magnitude with increasing volume fraction of kerogen.  相似文献   
42.
Diffusion parameters for hydrogen diffusion in epidote-group minerals and micas have been measured under hydrothermal conditions, or calculated from existing experimental data, for bulk hydrogen isotope exchange experiments between hydrous minerals and water. Activation energies in the range 14 to 31 kcals/g-atom H are comparable to those derived by application of kinetic theory to experimental hydrogen isotope exchange data, and to those for oxygen diffusion in minerals under hydrothermal conditions. Diffusion of hydrogen in epidote is about four orders of magnitude faster than in muscovite, and about two orders of magnitude faster than in zoisite. Hydrogen diffusion in micas is about five orders of magnitude faster than oxygen diffusion, and hydrogen transport occurs dominantly parallel to the layers rather than parallel to the c-axis as for oxygen.Rapid hydrogen transport in minerals may proceed by hydrolysis of Si-O and Al-O bonds, followed by exchange of hydrolyzed oxygens with slower-diffusing (OH) or H2O. Water appears to be essential for stable isotope exchange between minerals in slowly cooling metamorphic rocks.Stable isotope data for regional metamorphic mineral assemblages suggests that water is usually present in small amounts during cooling of prograde regional metamorphic systems, and estimated closure temperatures for cessation of stable isotope exchange are often more comparable to those calculated from diffusion data than to likely temperatures of metamorphism.Alpine deformation of the Hercynian Monte Rose Granite (Frey et al. 1976) permitted access of water and initiated stable isotope exchange amongst coexisting minerals. The diffusional behaviour of species in relict Hercynian muscovites is consistent with available experimental diffusion data.  相似文献   
43.
We present an 8000‐year history spanning 650 km of ice margin retreat for the largest marine‐terminating ice stream draining the former British–Irish Ice Sheet. Bayesian modelling of the geochronological data shows the ISIS expanded 34.0–25.3 ka, accelerating into the Celtic Sea to reach maximum limits 25.3–24.5 ka before a collapse with rapid marginal retreat to the northern Irish Sea Basin (ISB). This retreat was rapid and driven by climatic warming, sea‐level rise, mega‐tidal amplitudes and reactivation of meridional circulation in the North Atlantic. The retreat, though rapid, is uneven, with the stepped retreat pattern possibly a function of the passage of the ice stream between normal and adverse ice bed gradients and changing ice stream geometry. Initially, wide calving margins and adverse slopes encouraged rapid retreat (~550 m a?1) that slowed (~100 m a?1) at the topographic constriction and bathymetric high between southern Ireland and Wales before rates increased (~200 m a?1) across adverse bed slopes and wider and deeper basin configuration in the northern ISB. These data point to the importance of the ice bed slope and lateral extent in predicting the longer‐term (>1000 a) patterns and rates of ice‐marginal retreat during phases of rapid collapse, which has implications for the modelling of projected rapid retreat of present‐day ice streams. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
44.
We quantify and compare different measures of potential propagule pressure (PPP) of aquatic invasive species (AIS) from commercial vessels in Canada. We used ship arrivals and ballast water discharge volumes as proxies for PPP from ballast water organisms, and wetted surface area (WSA) as a proxy for hull fouling PPP, to determine their relative contributions to total PPP. For three regions studied, PPP proxies correlated significantly across ports and some vessel categories. Relative contributions of ship arrivals, ballast discharge, and WSAs to PPP, evidenced by non-significant correlations across these measures, varied across regions, ports, vessel types, and seasons. Flow-through (dominant on east and west coasts) and empty-refill (in Great Lakes-St. Lawrence region) were the major ballast water exchange methods employed by the vessels surveyed. These methods have different biological efficacy for AIS removal, influencing PPP. Our study illustrates benefits and limitations of using different PPP proxies to estimate invasion risk.  相似文献   
45.
Nickel speciation in a nickel hyperaccumulating plant (Sebertia acuminata) and its associated soil of southern New Caledonia was studied using various analytical methods. The soil is formed of iron oxides (goethite, hematite), which contain almost all the nickel. The available nickel is probably linked to the organic matter in the litter. Sebertia acuminata, acts as a nickel pump, and concentrates the metal in its leaves. It partitions nickel and silica; nickel is concentrated in the cells (probably in the vacuoles) as organometallic complexes, whereas silica forms the framework of the cells, and the phytolithes. A thorough study of these plants seems essential in order to define the soil–plant relations, and to propose appropriate ways for ecological restoration. To cite this article: N. Perrier et al., C. R. Geoscience 336 (2004).  相似文献   
46.
Probabilistic domain decomposition is proposed as a novel method for solving the two-dimensional Maxwell’s equations as used in the magnetotelluric method. The domain is split into non-overlapping sub-domains and the solution on the sub-domain boundaries is obtained by evaluating the stochastic form of the exact solution of Maxwell’s equations by a Monte-Carlo approach. These sub-domains can be naturally chosen by splitting the sub-surface domain into regions of constant (or at least continuous) conductivity. The solution over each sub-domain is obtained by solving Maxwell’s equations in the strong form. The sub-domain solver used for this purpose is a meshless method resting on radial basis function-based finite differences. The method is demonstrated by solving a number of classical magnetotelluric problems, including the quarter-space problem, the block-in-half-space problem and the triangle-in-half-space problem.  相似文献   
47.
Eluvial concentration of platinum-group minerals (PGM) has developed in the south of New Caledonia, from the weathering of a mafic and ultramafic cumulate. The platinum/palladium (Pt/Pd) ratio evolution from the bottom to the top of the weathering profile indicates a chemical mobilization of Pd in supergene environment. The examination by scanning electron microscopy of the residual PGM collected in the weathering profile and their chemical characterization by electronic microprobe show a preservation of the structure and chemical signature (in the core of the grains) of the fresh PGM. This clearly demonstrates that the PGM studied here are residual and are affected by dissolution process.  相似文献   
48.
The breakdown of potassium feldspar at high water pressures   总被引:1,自引:0,他引:1  
The equilibrium position of the reaction between sanidine and water to form “sanidine hydrate” has been determined by reversal experiments on well characterised synthetic starting materials in a piston cylinder apparatus. The reaction was found to lie between four reversed brackets of 2.35 and 2.50 GPa at 450 °C, 2.40 and 2.59 GPa at 550 °C, 2.67 and 2.74 GPa at 650 °C, and 2.70 and 2.72 GPa at 680 °C. Infrared spectroscopy showed that the dominant water species in sanidine hydrate was structural H2O. The minimum quantity of this structural H2O, measured by thermogravimetric analysis, varied between 4.42 and 5.85 wt% over the pressure range of 2.7 to 3.2 GPa and the temperature range of 450 to 680 °C. Systematic variation in water content with pressure and temperature was not clearly established. The maximum value was below 6.07 wt%, the equivalent of 1 molecule of H2O per formula unit. The water could be removed entirely by heating at atmospheric pressure to produce a metastable, anhydrous, hexagonal KAlSi3O8 phase (“hexasanidine”) implying that the structural H2O content of sanidine hydrate can vary. The unit cell parameters for sanidine hydrate, measured by powder X-ray diffraction, were a = 0.53366 (±0.00022) nm and c = 0.77141 (±0.00052) nm, and those for hexasanidine were a = 0.52893 (±0.00016) nm and c = 0.78185 (±0.00036) nm. The behaviour and properties of sanidine hydrate appear to be analogous to those of the hydrate phase cymrite in the equivalent barium system. The occurrence of sanidine hydrate in the Earth would be limited to high pressure but very low temperature conditions and hence it could be a potential reservoir for water in cold subduction zones. However, sanidine hydrate would probably be constrained to granitic rock compositions at these pressures and temperatures. Received: 6 May 1997 / Accepted: 2 October 1997  相似文献   
49.
50.
Considerable uncertainty surrounds the timing of glacier advance and retreat during the Younger Dryas or Loch Lomond Stade (LLS) in the Scottish Highlands. Some studies favour ice advance until near the end of the stade (c. 11.7 ka), whereas others support the culmination of glacier advance in mid‐stade (c. 12.6–12.4 ka). Most published 10 Be exposure ages reported for boulders on moraines or deglacial sites post‐date the end of the LLS, and thus appear to favour the former view, but recalibration of 33 10 Be ages using a locally derived 10 Be production rate and assuming rock surface erosion rates of zero to 1 mm ka?1 produces exposure ages 130–980 years older than those originally reported. The recalibrated ages are filtered to exclude anomalous data, and then employed to generate aggregate probability density distributions for the timing of moraine deposition and deglaciation. The results suggest that the most probable age for the timing of the deposition of the sampled outermost moraines lies in the interval 12.4–12.1 ka or earlier. Deglacial ages obtained for sites inside Loch Lomond Stadial glacier limits imply that glaciers at some or all of the sampled sites were retreating prior to 12.1 ka. Use of aggregated data does not exclude the possibility of asynchronous glacier behaviour at different sites, but confirms that some glaciers reached their maximum limits and began to retreat several centuries before the rapid warming that terminated the LLS at 11.7–11.6 ka, consistent with the retrodictions of recent numerical modelling experiments and with geomorphological evidence for gradual oscillatory ice‐margin retreat under stadial conditions.  相似文献   
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