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11.
Precise hydrogeochemical modeling of early diagenesis is a key in the reconstruction of sedimentary basin models. This determines the mineralogical evolution of the sediment and consequently the porosity of the rock. During early diagenesis also part of the initial organic matter is converted into biogenic gas: CH4 CO2, and H2S. These processes are part of complex reaction chains during sedimentation, and biogeochemical reactions leave different signals that can be observed today. In this work, we reproduce the early diagenetic processes as integrated signals over geological times in sediments of the Demerara Rise by applying chemical thermodynamics using the PHREEQC (version 2) computer code. The investigated sediments are characterized by the presence of black shales in 410–490 mbsf and by a diagenetic barite layer above in 300–350 mbsf at depth of sulfate-methane transition (SMT). We determine the parameters that influence the location of diagenetic barite peaks in sediments overlying black shales by means of a novel modeling approach. Crucial parameters are the amount of bacterial organic matter mineralization, sedimentation rates and bottom water sulfate concentrations. All parameters are intertwining and influence the sulfate-methane cycle. They affect the location of the SMT visualized by diagenetic barite peaks. However, our model approach opens a wide field in exploring early diagenetic reactions, processes and products (such as biogenic methane) over geological times mirrored by diagenetic minerals and pore water concentration profiles that can be detected in present-day sediments.  相似文献   
12.
MultiBeam echosounder data were collected during a surface-ship survey of the 22/4b well site in the North Sea in September 2011 using a Teledyne-Reson 7125. Modern multibeam echosounders are instrumental in providing detection and accurate localization of weak to strong bubble plumes. Two survey profiles effectively insonified the bubble plumes rising from the main crater at the well site, providing snapshot data of bubble plume processes. Additionally, three profiles insonified bubble plumes rising from, in, and to the south of a secondary crater, 1.2 km southeast of the main crater. Data processing included a simple algorithm that muted mislocated echoes from incomplete sidelobe suppression. The data processing produced a Cartesian volume of echo intensity from the water column and seabed.Plume geometry was analyzed to investigate a number of important large-scale plume processes, including plume bubble detrainment due to currents and stratification, downwelling flows, sea surface interaction, plume heterogeneity, and other fluid transport processes. The data showed strong upwelling flows, with bubble vertical motions generally much faster than currents. One important finding was that megaplumes create intrusions above the general thermocline, in part because their extensive upwelling flow lifts the thermocline locally. As a result, the intrusion layer deposits dissolved gases in the upper wave-mixed layer of the water column where it is not isolated from the atmosphere, unlike dissolved gases in the lower water column.The analysis shows that high fidelity multibeam echosounder data can provide a wealth of remote sensing information on bubble plume characteristics and processes, with important applications, including blowout monitoring and response, better understanding of megaplumes such as used in lake destratification, and improved characterization of natural seep emission processes.  相似文献   
13.
Nearly 2000 pockmarks with diameters ranging from a few tens of meters up to 700 m are present on the seafloor of the St. Lawrence Estuary in eastern Canada. Coring of some pockmarks resulted in the recovery of various-sized and shaped carbonate concretions in a predominantly silty mud matrix. Petrographic and geochemical data on four authigenic carbonate concretions are reported as well as data from shell material in the unconsolidated sediment. Video observations and echo-sounder images indicate that the sampled pockmarks are actively gas venting. The video images show significant look-alike microbial mats in areas where gas is venting. The carbonate concretions are primarily made up of carbonate cements with varying percentage of shell fragments, micrite particles and fine-grained clastics. Orthorhombic crystal morphology and diagenetic fabrics including isopachous layers and botryoids characterize the aragonite cement. Oxygen isotopes ratios for the cement crusts do not record any thermal anomaly at the site of precipitation with δ18OVPDB ratios (+3) in equilibrium with cold (5 °C) deep marine waters, whereas significant negative δ13CVPDB ratios (−9.9 to −33.5) for cement and shell material within concretions indicate that the carbonates largely derive from the microbial oxidation of methane. The δ13CVPDB ratios of aragonite shells (−2.7 to −5.6) taken from unconsolidated sediments at some distance from the concretions/vents show variable dilution of HCO3 with negative δ13CVPDB ratios derived from microbial oxidation of methane with isotopically normal (0) marine bicarbonate. These results are in agreement with other lines of evidence suggesting that pockmarks formed through the recent and still active release of gas from a reservoir within the Paleozoic sedimentary succession.  相似文献   
14.
湿地甲烷排放研究简述   总被引:4,自引:2,他引:4  
马学慧  李君泉 《地理科学》1995,15(2):163-169
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15.
Results of more than 800 new measurements of methane (CH4) concentrations in the Southern Hemisphere troposphere (34–41° S, 130–150° E) are reported. These were obtained between September 1980 and March 1983 from the surface at Cape Grim, Tasmania, through the middle (3.5–5.5 km) to the upper troposphere (7–10 km). The concentration of CH4 increased throughout the entire troposphere over the measurement period, adding further support to the view that CH4 concentrations are currently increasing on a global scale. For data averaged vertically through the troposphere the rate of increase found was 20 ppbv/yr or 1.3%/yr at December 1981. In the surface CH4 data a seasonal cycle with a peak to peak amplitude of approximately 28 ppbv is seen, with the minimum concentration occurring in March and the maximum in September–October. A cycle with the same phase as that seen at the surface, but with a significantly decreased amplitude, is apparent in the mid troposphere but no cycle is detected in the upper tropospheric data. The phase and amplitude of the cycle are qualitatively in agreement with the concept that the major sink for methane is oxidation by hydroxyl radicals. Also presented is evidence of a positive vertical gradient in methane, with a suggestion that the magnitude of this gradient has changed over the period of measurements.  相似文献   
16.
The global distribution of methane in the troposphere   总被引:6,自引:0,他引:6  
Methane has been measured in air samples collected at approximately weekly intervals at 23 globally distributed sites in the NOAA/GMCC cooperative flask sampling network. Sites range in latitude from 90° S to 76° N, and at most of these we report 2 years of data beginning in early 1983. All measurements have been made by gas chromatography with a flame ionization detector at the NOAA/GMCC laboratory in Boulder, Colorado. All air samples have been referenced to a single secondary standard of methane-in-air, ensuring a high degree of internal consistency in the data. The precision of measurements is estimated from replicate determinations on each sample as 0.2%. The latitudinal distribution of methane and the seasonal variation of this distribution in the marine boundary layer has been defined in great detail, including a remarkable uniformity in background levels of methane in the Southern Hemisphere. We report for the first time the observation of a complete seasonal cycle of methane at the South Pole. A significant vertical gradient is observed between a sea level and a high altitude site in Hawaii. Globally averaged background concentrations in the marine boundary layer have been calculated for the 2 year-period May 1983–April 1985 inclusive, from which we find an average increase of 12.8 ppb per year, or 0.78% per year when referenced to the globally averaged concentration (1625 ppb) at the mid-point of this period. We present evidence that there has been a slowing down in the methane growth rate.Presented at the Conference on the Scientific Application of Baseline Observations of Atmospheric Composition (SABOAC), Aspendale, Australia, 7–9 November 1984.  相似文献   
17.
New CH4 emission data from a number of Northern and Southern Hemispheric, tropical and temperate termites, are reported, which indicate that the annual global CH4 source due to termites is probably less than 15 Tg. The major uncertainties in this estimate are identified and found to be substantial. Nevertheless, our results suggest that termites probably account for less than 5% of global CH4 emissions.  相似文献   
18.
广州地区稻田甲烷排放及中国稻田甲烷排放的空间变化   总被引:13,自引:0,他引:13  
1993年在广州地区采用中国科学院大气物理研究所研制的自动采集和分析系统测量了稻田甲烷的排放率,首次获得了占我国20-25%左右水稻收获面积的华南地区稻田甲烷排放特征值。从而宏观地使我国五个主要水稻生态区的甲烷排放率都有了实测资料。稻田甲烷排放率的季节变化主要与气温及灌溉水状态的变化的较大关系,日变化规律以下午出现极大为主。本实验田的甲烷排放率低。  相似文献   
19.
封闭系统中多孔介质甲烷水合物的CT实验研究   总被引:2,自引:0,他引:2  
阐述了在封闭系统中的查理模型,建立了利用查理定律计算分析甲烷水合物生成和分解的方法。通过实验,对封闭系统中不同含水量多孔介质甲烷水合物生成、发育和分解的实验方法、相平衡条件、生成量关系等进行了探讨。在一定温度差的介质里,水分克服重力向冷端迁移并生成水合物。实验中利用查理数的改变计算水合物的生成量变化,连通性好的含水多孔介质有很好的水—气结合条件,达到平衡条件后迅速生成水合物,在240分钟内完成,含水量线性地影响甲烷水合物的生成量。同时,利用CT扫描方法直接观测含水粗砂在低温—高压环境下的甲烷水合物生成和分解过程,并可以利用CT图像数据计算出多孔介质中水分迁移、区域密度改变和砂体的移动、及分解后介质密度分布变化特征。  相似文献   
20.
High-pressure Raman studies of methane hydrate were performed using a diamond anvil cell in the pressure range of 0.1–86 GPa at room temperature. Raman spectra of the methane molecules revealed that new softened intramolecular vibration mode of ν 1 appeared at 17 GPa and that the splitting of vibration mode of ν 3 occurred at 15 GPa. The appearance of these two modes indicates that an intermolecular attractive interaction increases between the methane molecules and the host water molecules and between the neighboring methane molecules. These interactions might result in the exceptional stability of a high-pressure structure, a filled ice Ih structure (FIIhS) for methane hydrate, up to 40 GPa. At 40 GPa, a clear change in the slope of the Raman shift versus pressure occurred, and above 40 GPa the Raman shift of the vibration modes increased monotonously up to 86 GPa. A previous XRD study showed that the FIIhS transformed into another new high-pressure structure at 40 GPa. The change in the Raman spectra at 40 GPa may be induced by the transition of the structure.  相似文献   
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