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201.
Marc S. Seigar Paul D. Lynam Nicole E. Chorney 《Monthly notices of the Royal Astronomical Society》2003,344(1):110-114
We present a ground-based, near-infrared, K -band image and a Hubble Space Telescope ( HST ) WFPC2 image of the brightest cluster galaxy in Abell 193 (IC 1695). This object was selected as the central cluster galaxy using X-ray information. Both images reveal a triple nucleus structure. Previously, this galaxy was thought to have only two nuclei. We present colours and magnitudes and a colour plot of the three nuclei. The nuclear structure and colours of the nuclei in this galaxy suggest that a merger may have taken place in its recent history. 相似文献
202.
Catherine Dupas-Bruzek Tracy N. Tingle Harry W. Green II. Nicole Doukhan Jean-Claude Doukhan 《Physics and Chemistry of Minerals》1998,25(7):501-514
Synthetic polycrystals of α-Mg2GeO4 (with the olivine structure) and γ-Mg2GeO4 (with the spinel structure) deformed at high temperature and pressure in their respective stability fields were investigated by analytical transmission electron microscopy. Specimens with a mean grain size of 20–30 µm deform by dislocation glide and/or climb. The predominance of glide versus climb depends on stress and grain orientation. The defect microstructures of both polymorphs are very similar to those observed in their respective silicate analogues, α- and γ-(Mg,Fe)2SiO4, and, in the case of the spinel phase, very similar to those observed in magnesium aluminate spinels. These observations suggest that Mg2GeO4 is a good rheological analogue for the Earth’s upper mantle. A spinel specimen deformed under the same conditions of temperature and strain rate as an olivine specimen was approximately three times stronger than olivine. In specimens of both phases deformed at or above 1400 K, a thin amorphous film composed of Mg, Ge, and O was detected along some grain boundaries. Grains ≤10 µm diameter surrounded by a film of amorphous phase (>10 nm thick) exhibited low dislocation densities, and deformation appeared to have occurred by grain boundary sliding. 相似文献
203.
Karine Issautier Nicole Meyer-Vernet Viviane Pierrard Joseph Lemaire 《Astrophysics and Space Science》2001,277(1-2):189-193
We use a kinetic collisionless model of the solar wind to calculate the radial variation of the electron temperature and obtain
analytical expressions at large radial distances. In order to be compared with Ulysses observations, the model, which initially
assumed a radial magnetic field, has been generalized to a spiral magnetic field. We present a preliminary comparison with
Ulysses observations in the fast solar wind at high heliospheric latitudes.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
204.
205.
Patrick Huntjens Louis Lebel Claudia Pahl-Wostl Jeff Camkin Roland Schulze Nicole Kranz 《Global Environmental Change》2012,22(1):67-81
This paper provides an evidence-based contribution to understanding processes of climate change adaptation in water governance systems in the Netherlands, Australia and South Africa. It builds upon the work of Ostrom on institutional design principles for local common pool resources systems. We argue that for dealing with complexities and uncertainties related to climate change impacts (e.g. increased frequency and intensity of floods or droughts) additional or adjusted institutional design propositions are necessary that facilitate learning processes. This is especially the case for dealing with complex, cross-boundary and large-scale resource systems, such as river basins and delta areas in the Netherlands and South Africa or groundwater systems in Western Australia. In this paper we provide empirical support for a set of eight refined and extended institutional design propositions for the governance of adaptation to climate change in the water sector. Together they capture structural, agency and learning dimensions of the adaptation challenge and they provide a strong initial framework to explore key institutional issues in the governance of adaptation to climate change. These institutional design propositions support a “management as learning” approach to dealing with complexity and uncertainty. They do not specify blueprints, but encourage adaptation tuned to the specific features of local geography, ecology, economies and cultures. 相似文献
206.
Elevated As concentrations have been measured in wells in the St. Peter Sandstone aquifer of eastern Wisconsin, USA. The primary source is As-bearing sulfide minerals (pyrite and marcasite) within the aquifer. There is concern that well disinfection by chlorination may facilitate As release to groundwater by increasing the rate and extent of sulfide oxidation. The objective of this study was to examine the abiotic processes that mobilize As from the aquifer solids during controlled exposure to chlorinated solutions. Thin sections made from sulfidic aquifer material were characterized by quantitative electron probe micro-analysis before and after 24 h exposure to solutions of different Cl2 concentrations. Batch experiments using crushed aquifer solids were also conducted to examine changes in solution chemistry over 24 h. Results of the combined experiments indicate that Cl2 addition affects As release and uptake in two ways. First, Cl2 increases oxidation of sulfide minerals, releasing more As from the mineral structure. Chlorine addition also increases the rate of Fe(II) oxidation and subsequent hydrous ferric oxide (HFO) precipitation, allowing for increased uptake of As onto the mineral surface. Although HFOs can act as sinks for As, they can release As if biogeochemical conditions (e.g. redox, pH) change. These results have implications not only for disinfection of drinking water wells in the study area, but also suggest that introduction of oxidants may adversely affect water quality during aquifer storage and recovery programs in aquifers containing As-bearing minerals. 相似文献
207.
208.
Filippo Pantellini Soraya Belheouane Nicole Meyer-Vernet Arnaud Zaslavsky 《Astrophysics and Space Science》2012,341(2):309-314
High rate sampling detectors measuring the potential difference between the main body and boom antennas of interplanetary spacecraft have been shown to be efficient means to measure the voltage pulses induced by nano dust impacts on the spacecraft body itself (see Meyer-Vernet et al. in Sol. Phys. 256:463, 2009). However, rough estimates of the free charge liberated in post impact expanding plasma cloud indicate that the cloud’s own internal electrostatic field is too weak to account for measured pulses as the ones from the TDS instrument on the STEREO spacecraft frequently exceeding 0.1 V/m. In this paper we argue that the detected pulses are not a direct measure of the potential structure of the plasma cloud, but are rather the consequence of a transitional interruption of the photoelectron return current towards the portion of the antenna located within the expanding cloud. 相似文献
209.
Benjamin Rotenberg Jean-Pierre Morel Pierre Turq Nicole Morel-Desrosiers 《Geochimica et cosmochimica acta》2009,73(14):4034-20527
We study the origin of the ionic exchange enthalpy in montmorillonite clays using microcalorimetry measurements and molecular simulation. We first determine the standard reaction enthalpy for well-defined interlayer water contents. We then show by a detailed analysis based on thermodynamic cycles that replacing Na+ ions by Cs+ in the interlayer of montmorillonite clays is an endothermic process, and that the overall exchange is exothermic only because it is dominated by the exothermic replacement of Cs+ by Na+ in the aqueous phase. This conclusion from ionic exchange enthalpies supports the one of a recent study of the ionic exchange free energy by Teppen and Miller [Teppen B. J. and Miller D. M. (2006) Hydration energy determines isovalent cation exchange selectivity by clay minerals. Soil Sci. Soc. Am. J.70(1), 31-40] and contradicts long-held views on the role of ion-clay interactions in determining the ionic exchange thermodynamics. This calls for a paradigm shift for the origin of this exchange: The driving force is the “hydrophobicity” of Cs+ compared to Na+ and not its affinity for clay surfaces. 相似文献
210.
The oxidation state of sulfur in synthetic and natural glasses determined by X-ray absorption spectroscopy 总被引:1,自引:0,他引:1
Sulfur K-edge X-ray absorption near edge structure (XANES) spectra were recorded for experimental glasses of various compositions prepared at different oxygen fugacities (fO2) in one-atmosphere gas-mixing experiments at 1400 °C. This sample preparation method only results in measurable S concentrations under either relatively reduced (log fO2 < −9) or oxidised (log fO2 > −2) conditions. The XANES spectra of the reduced samples are characterised by an absorption edge crest at 2476.4 eV, typical of S2−. In addition, spectra of Fe-bearing compositions exhibit a pronounced absorption edge shoulder. Spectra for all the Fe-free samples are essentially identical, as are the spectra for the Fe-bearing compositions, despite significant compositional variability within each group. The presence of a sulfide phase, such as might exsolve on cooling, can be inferred from a pre-edge feature at 2470.5 eV.The XANES spectra of the oxidised samples are characterised by an intense transition at 2482.1 eV, typical of the sulfate anion SO42−. Sulfite (SO32−) has negligible solubility in silicate melts at low pressures. The previous identification of sulfite species in natural glass samples is attributed to an artefact of the analysis (photoreduction of S6+). S4+ does, however, occur unambiguously with S6+ in Fe-free and Fe-poor compositions prepared in equilibrium with CaSO4 at 4-16 kbar, and when buffered with Re/ReO2 at 10 kbar. Solubility of S4+ thus requires partial pressures of SO2 considerably in excess of 1 bar. A number of experiments were undertaken in an attempt to access intermediate fO2s more applicable to terrestrial volcanism. Although these were largely unsuccessful, S2− and S6+ were found to coexist in some samples that were not in equilibrium with the imposed fO2.The XANES spectra of natural olivine-hosted melt inclusions and submarine glasses representative of basalts at, or close to, sulfide saturation show mainly dissolved S2−, but with minor sulfate, and additionally a peak at 2469.5 eV, which, although presumably due to immiscible sulfide, is 1 eV lower than that typical of FeS. These sulfate and sulfide-related peaks disappear with homogenisation of the inclusions by heating to 1200 °C followed by rapid quenching, suggesting that both these features are a result of cooling under natural conditions. The presence of small amounts of sulfate in otherwise reduced basaltic magmas may be explained by the electron exchange reaction: S2− + 8Fe3+ = S6+ + 8Fe2+, which is expected to proceed strongly to the right with decreasing temperature. This reaction would explain why S2− and S6+ are frequently found together despite the very limited fO2 range over which they are thermodynamically predicted to coexist. The S XANES spectra of water-rich, highly oxidised, basaltic inclusions hosted in olivine from Etna and Stromboli confirm that nearly all S is dissolved as sulfate, explaining their relatively high S contents. 相似文献