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One-hundred fluid inclusions in Silurian marine halite were analyzed in order to determine the major-ion composition of Silurian seawater. The samples analyzed were from three formations in the Late Silurian Michigan Basin, the A-1, A-2, and B Evaporites of the Salina Group, and one formation in the Early Silurian Canning Basin (Australia), the Mallowa Salt of the Carribuddy Group. The results indicate that the major-ion composition of Silurian seawater was not the same as present-day seawater. The Silurian ocean had lower concentrations of Mg2+, Na+, and SO42−, and much higher concentrations of Ca2+ relative to the ocean’s present-day composition. Furthermore, Silurian seawater had Ca2+ in excess of SO42−. Evaporation of Silurian seawater of the composition determined in this study produces KCl-type potash minerals that lack the MgSO4-type late stage salts formed during the evaporation of present-day seawater. The relatively low Na+ concentrations in Silurian seawater support the hypothesis that oscillations in the major-ion composition of the oceans are primarily controlled by changes in the flux of mid-ocean ridge brine and riverine inputs and not global or basin-scale, seawater-driven dolomitization. The Mg2+/Ca2+ ratio of Silurian seawater was ∼1.4, and the K+/Ca2+ ratio was ∼0.3, both of which differ from the present-day counterparts of 5 and 1, respectively. Seawaters with Mg2+/Ca2+ <2 facilitate the precipitation of low-magnesian calcite (mol % Mg < 4) marine ooids and submarine carbonate cements whereas seawaters with Mg2+/Ca2+ >2 (e.g., modern seawater) facilitate the precipitation of aragonite and high-magnesian calcite. Therefore, the early Paleozoic calcite seas were likely due to the low Mg2+/Ca2+ ratio of seawater, not the pCO2 of the Silurian atmosphere. 相似文献
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In recent years, many city authorities in Europe and North America have sought to attract people back to city centres for leisure, shopping, business and residence. The planning measures commonly adopted take explicit account of issues of crime and safety. The concept of `community safety' as applied to the city centre is problematic, however, as users have diverse lifestyles, interests and values which impact on their own and others' safety. This paper reports on a study of the experiences and perceptions of safety of different groups of city centre users in Newcastle upon Tyne, England. While social identities and roles shaped the extent of concern and subsequent impacts on people's use of the city centre space, the research suggested that many concerns are genuinely shared. The paper investigates the congruence of a range of planning strategies with city centre users' safety concerns. Situational measures were viewed with scepticism, as fear centres on the presence and behaviour of others. 相似文献
15.
Padinare V. Unnikrishna Jeffrey J. McDonnell Carol Kendall 《Journal of Hydrology》2002,260(1-4):38-57
Isotopic variations in melting snow are poorly understood. We made weekly measurements at the Central Sierra Snow Laboratory, California, of snow temperature, density, water equivalent and liquid water volume to examine how physical changes within the snowpack govern meltwater δ18O. Snowpack samples were extracted at 0.1 m intervals from ground level to the top of the snowpack profile between December 1991 and April 1992. Approximately 800 mm of precipitation fell during the study period with δ18O values between −21.35 and −4.25‰. Corresponding snowpack δ18O ranged from −22.25 to −6.25‰. The coefficient of variation of δ18O in snowpack levels decreased from −0.37 to −0.07 from winter to spring, indicating isotopic snowpack homogenization. Meltwater δ18O ranged from −15.30 to −8.05‰, with variations of up to 2.95‰ observed within a single snowmelt episode, highlighting the need for frequent sampling. Early snowmelt originated in the lower snowpack with higher δ18O through ground heat flux and rainfall. After the snowpack became isothermal, infiltrating snowmelt displaced the higher δ18O liquid in the lower snowpack through a piston flow process. Fractionation analysis using a two-component mixing model on the isothermal snowpack indicated that δ18O in the initial and final half of major snowmelt was 1.30‰ lower and 1.45‰ higher, respectively, than the value from simple mixing. Mean snowpack δ18O on individual profiling days showed a steady increase from −15.15 to −12.05‰ due to removal of lower δ18O snowmelt and addition of higher δ18O rainfall. Results suggest that direct sampling of snowmelt and snow cores should be undertaken to quantify tracer input compositions adequately. The snowmelt sequence also suggests that regimes of early lower δ18O and later higher δ18O melt may be modeled and used in catchment tracing studies. 相似文献
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Placing geographies of public health 总被引:6,自引:0,他引:6
Following the move to a 'post–medical' geography, a large amount of research has come to focus on public health issues. This paper explores these current geographies of public health and argues for the development of a more critical perspective. In particular, it draws on commentary that has emerged out of debates that have taken place within a body of literature usually identified as the critical 'new' public health. The paper goes on to argue that such scholarship offers crucial insights for the production of a critical geography of public health. 相似文献
18.
Gerrit de Leeuw Lucinda Spokes Tim Jickells Carsten Ambelas Skjth Ole Hertel Elisabetta Vignati Susanne Tamm Michael Schulz Lise-Lotte Srensen Britta Pedersen Laura Klein K. Heinke Schlünzen 《Continental Shelf Research》2003,23(17-19):1743
The ANICE (Atmospheric Nitrogen Inputs into the Coastal Ecosystem) project addressed the atmospheric deposition of nitrogen to the North Sea, with emphasis on coastal effects. ANICE focused on quantifying the deposition of inorganic nitrogen compounds to the North Sea and the governing processes. An overview of the results from modelling and experimental efforts is presented. They serve to identify the role of the atmosphere as a source of biologically essential chemical species to the marine biota. Data from the Weybourne Atmospheric Observatory (UK) are used to evaluate the effect of short episodes with very high atmospheric nitrogen concentrations. One such episode resulted in an average deposition of 0.8 mmol N m−2 day−1, which has the potential to promote primary productivity of 5.3 mmol C m−2 day−1. This value is compared to long-term effects determined from model results. The total calculated atmospheric deposition to the North Sea in 1999 is 948 kg N km−1, i.e. 0.19 mmol N m−2 day−1 which has the potential to promote primary productivity of 1.2 mmol C m−2 day−1. Detailed results for August 1999 show strong gradients across the North Sea due to adjacent areas where emissions of NOx and NH3 are among the highest in Europe. The average atmospheric deposition to the southern part of the North Sea in August 1999 could potentially promote primary production of 2.0 mmol C m−2 day−1, i.e. 5.5% of the total production at this time of the year in this area of the North Sea. For the entire study area the atmospheric contribution to the primary production per m2 is about two-third of this value. Most of the deposition occurs during short periods with high atmospheric concentrations. This atmospheric nitrogen is almost entirely anthropogenic in origin and thus represents a human-induced perturbation of the ecosystem. 相似文献
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The forces of interaction were measured between the siderophore azotobactin and the minerals goethite (α-FeOOH) and diaspore (α-AlOOH) in aqueous solution using force microscopy. Azotobactin, a pyoverdin-type siderophore, was covalently linked to a hydrazide terminated atomic force microscope tip using a standard active ester protein coupling technique. Upon contact with each mineral surface, the adhesion force between azotobactin and goethite was two to three times the value observed for the isostructural Al-equivalent diaspore. The affinity for the solid iron oxide surface reflected in the force measurements correlates with the specificity of azotobactin for aqueous ferric iron. Further, the adhesion force between azotobactin and goethite significantly decreases (4 nN to 2 nN) when small amounts of soluble iron (0.1 μM FeCl3 · 6H2O) are added to the system at pH 3.5 suggesting a significant specific interaction between the chelating reactive center of azotobactin and the mineral surface. Changes in the force signature with pH and ionic strength were fairly predictable when considering mineral solubility, the charge character of the mineral surfaces, the molecular structure of azotobactin, and the intervening solution. For example, azotobactin-goethite adhesion values were consistently smaller at pH 3.5 relative to the forces at pH 7. At the lower pH, the large number of protons and the increase in the mineral solubility provides additional electron acceptors (e.g., H+ and Fe3+(aq)) that are free to compete for the basic oxygen chelating sites in the azotobactin structure. It is believed that this competition disrupts siderophore affinity for the surface resulting in decreased adhesion values. 相似文献