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51.
中国地区气溶胶的辐射强迫及其气候响应试验 总被引:15,自引:3,他引:12
根据国内测定的排放因子数据和国家、部委及各省市统计年鉴公布的排放源数据,得到的中国大陆的1°×1°网格精度的SO2的排放分布,计算了中国地区人为扰动气溶胶的辐射强迫。应用近期开发的二维能量平衡模式计算了由该种气溶胶所引起的中国地区地面温度变化。模式结果表明,最大辐射强迫和最大地面温度变化都集中在中国的沿海和四川地区。最大辐射强迫达3 W/m2。 相似文献
52.
A Three-Dimensional Global Model Study of Carbonyl Sulfide in the Troposphere and the Lower Stratosphere 总被引:4,自引:0,他引:4
Erik Kjellström 《Journal of Atmospheric Chemistry》1998,29(2):151-177
Global distributions of carbonyl sulfide and carbon disulfide have been calculated with a three-dimensional global model of the atmospheric general circulation (ECHAM). The model calculates a global sink strength for carbonyl sulfide of 0.3 Tg S yr-1, with vegetation uptake being the largest sink. With this sink strength, the sources have to be close to the lower limit of the present estimate in the literature. The calculated mixing ratios are higher in the Southern Hemisphere than in the Northern Hemisphere. This interhemispheric gradient is the opposite of what is observed demonstrating that the present knowledge of the distribution of sinks and sources is not fully adequate. The model calculations support the idea that the open oceans could act as a net sink of carbonyl sulfide. The calculated stratospheric photolysis of carbonyl sulfide constitutes about 4% of the total sink of carbonyl sulfide. A stratospheric production of sulfate from carbonyl sulfide of 0.013 Tg S yr-1 is obtained, which is 3 to 12 times less than what is needed to maintain the stratospheric sulfate aerosol layer. Although these results are associated with uncertainties, due to the low upper boundary and coarse vertical resolution of the model, they support recent findings of a low stratospheric production of sulfate from carbonyl sulfide. Instead, sulfur dioxide transported from the troposphere is calculated to be the most important precursor for the stratospheric sulfate aerosol layer. 相似文献
53.
陆相咸化湖泊沉积硫酸盐岩硫同位素组成及其地质意义 总被引:1,自引:0,他引:1
现代海洋中的硫酸盐矿物和海水硫酸盐本身常有相似的硫同位素组成,因而可根据现代蒸发岩的硫酸盐同位素来判断古环境。据李任伟[1]引用Holser和Kaplan及格里年科的资料报道,海相蒸发岩及其所反映的古海洋硫酸盐的硫同位素组成只在较狭窄的范围内变化,现... 相似文献
54.
The biogeochemical sulfur cycle in the marine boundary layer over the Northeast Pacific Ocean 总被引:1,自引:0,他引:1
T. S. Bates J. E. Johnson P. K. Quinn P. D. Goldan W. C. Kuster D. C. Covert C. J. Hahn 《Journal of Atmospheric Chemistry》1990,10(1):59-81
The major components of the marine boundary layer biogeochemical sulfur cycle were measured simultaneously onshore and off the coast of Washington State, U.S.A. during May 1987. Seawater dimethylsulfide (DMS) concentrations on the continental shelf were strongly influenced by coastal upwelling. Concentration further offshore were typical of summer values (2.2 nmol/L) at this latitude. Although seawater DMS concentrations were high on the biologically productive continental shelf (2–12 nmol/L), this region had no measurable effect on atmospheric DMS concentrations. Atmospheric DMS concentrations (0.1–12 nmol/m3), however, were extremely dependent upon wind speed and boundary layer height. Although there appeared to be an appreciable input of non-sea-salt sulfate to the marine boundary layer from the free troposphere, the local flux of DMS from the ocean to the atmosphere was sufficient to balance the remainder of the sulfur budget. 相似文献
55.
Annual wet deposition of excess sulfate at Macquarie Island has been estimated from 5 months of rainwater composition data covering the Austral summer of 1985/86. The resulting figure of 2.1±0.6 mmol/m2/yr is at the low end of previous estimates of maritime excess sulfate deposition by precipitation. Within estimated uncertainty limits this figure is consistent with the DMS emission flux which would be predicted for latitude 50°–60° S, based solely on available Northern Hemispheric DMS measurements.Temporarily at the International Meteorological Institute, Stockholm University, S-106 91, Stockholm, Sweden. 相似文献
56.
Abstract: Carbonate rocks of Cambrian (18 samples) and lower-middle Ordovician (11 samples) ages from South Korea were analyzed for sulfur contents of structurally substituted sulfate (SSS) and sulfides and their δ34 S values. The δ34 S values of SSS ranging from +25.9 to +45.2 permil, are averaged as +33.6 and +33.5 permil for the Cambrian and Ordovician rocks, respectively, which indicate high δ34 S values of the Cambro-Ordovician seawater. The SSS contents in the carbonate rocks are low being 2.9 to 17.3 ppm S (averaged as 7.0 ppm S). Sulfide sulfur, on the contrary, is much abundant containing 3 to 1,880 ppm S and the δ34 S values range widely between –17.6 and +31.1 permil. Sulfide sulfur of the studied rocks excluding impure carbonates has an average content of 187 ppm S and δ34 S value of +12.8 permil (n=24). The estimated δ34 S (sulfate–sulfide) values, which range from 13.8 to 25.4 permil in general with a few exceptions from 36.5 up to 52.3 permil for some impure carbonates, may provide evidence for the persistent oceanic anoxia with its temporary recovery during the Cambro-Ordovician time.
The SSS and sulfide sulfurs have often higher δ34 S values than the Mesozoic-Cenozoic ore sulfur (Ishihara et al., 2000). Since carbonate rocks are very reactive with circulating hydrothermal ore solution, high δ34 S values of the Korean ore deposits might be caused to some extent by 34 S enrichment from the host carbonates, resulting in the low SSS contents observed. 相似文献
The SSS and sulfide sulfurs have often higher δ
57.
在分散度不同的区域内进行区域采样用于水中硫酸根离子的测定,结果令人满意。应用此方法测定硫酸根离子的线性范围为200.0~3000mg/L;进样频率为120次/h;相对标准偏差为1.70% 相似文献
58.
矿床技术经济评价在地质勘查工作中占有重要地位。目前编写地质勘查报告都必须包括技术经济评价章节。但我国矿床技术经济评价的理论和方法还存在一些问题,某些评价方法和基本概念还不够统一。通过对投资回收期、净现值、总现值、销售成本、经营成本等参数的研究认为,矿床技术经济评价要进一步规范化。 相似文献
59.
Trace metals in acid sediments and waters, Pimpama catchment, southeast Queensland, Australia 总被引:2,自引:1,他引:2
The Pimpama River floodplain has developed over the last several thousand years as a result of sea-level fluctuations that
shaped the lower catchment and enabled the formation of sedimentary pyrite. The subsequent production of sulfuric acid due
to the oxidation of this pyrite enhances the breakdown of metal-bearing sediments and can lead to leaching of major and trace
metals into the waters of the region. The seasonal pattern of rainfall and current land-use activities are important aspects
that intensify the natural production of acid and influence the release and distribution of metals. To identify the source
and migration of metals in the Pimpama catchment and to understand the impact of pyrite oxidation on the distribution of metals
in sediments and waters, several components of the drainage system were analyzed: bedrock, sediments from river bed and bank,
and water. The elements analyzed in this study (V, Cr, Co, Ni, Cu, Zn and Pb) are all present in the bedrock material which
explains their occurrence in the unconsolidated sediments of the floodplain. These metals concentrate in the upper section
of the sedimentary sequence and their presence is related to clay minerals such as smectite, organic matter and iron phases.
However, Zn, Mo and Co occur in higher amounts than the local background and within standard shale. This comparison suggests
that the diagenetic processes alone cannot explain the higher concentrations and it is concluded that these metals also have
an anthropogenic source. The formation of sulfuric acid creates conditions for higher mobility of some metals, such as Cr,
Co, Ni, Cu, Zn, but does not affect less mobile ones such as Mo and Pb. Over the longterm, the production of acid influences
the breakdown of mineral phases and enhances the process of weathering. Over the short term, every rain event leaches acid
from sediments and mobilizes metals resulting in a substantial reduction in the quality of river water.
Received: 2 October 1998 · Accepted: 16 February 1999 相似文献
60.
William R. Stockwell 《Journal of Atmospheric Chemistry》1994,19(3):317-329
The rates and mechanisms of both gas and liquid phase reactions for the oxidation of sulfur dioxide play an important role in the production of atmospheric acids and aerosol particles. Rhodeet al. (1981) concluded that sulfate production rates were highly non-linear functions of sulfur dioxide emission rates. Their modelling study used an HO
x
termination mechanism for the HO—SO2 reaction in the gas-phase. Stockwell and Calvert (1983) determined that one of the products of the overall reaction of HO with sulfur dioxide was an HO2 radical. The National Research Council (1983) using a version of the Rhodeet al. (1981) model modified to include HO2 production from the HO—SO2 reaction concluded that sulfate production becomes much more linear with respect to reductions in sulfur dioxide emissions. However, the cause of this increased linearity was not explained by the National Research Council report. It is demonstrated that the increased linearity is due to the coupling of gas-phases and aqueous phase chemistry. The gas-phase sulfur dioxide oxidation mechanism has a very significant effect on hydrogen perodide production rates. 相似文献