全文获取类型
收费全文 | 3476篇 |
免费 | 503篇 |
国内免费 | 915篇 |
专业分类
测绘学 | 51篇 |
大气科学 | 502篇 |
地球物理 | 623篇 |
地质学 | 1907篇 |
海洋学 | 760篇 |
天文学 | 99篇 |
综合类 | 161篇 |
自然地理 | 791篇 |
出版年
2024年 | 22篇 |
2023年 | 76篇 |
2022年 | 194篇 |
2021年 | 164篇 |
2020年 | 154篇 |
2019年 | 194篇 |
2018年 | 148篇 |
2017年 | 147篇 |
2016年 | 178篇 |
2015年 | 193篇 |
2014年 | 250篇 |
2013年 | 292篇 |
2012年 | 257篇 |
2011年 | 276篇 |
2010年 | 166篇 |
2009年 | 255篇 |
2008年 | 259篇 |
2007年 | 189篇 |
2006年 | 218篇 |
2005年 | 170篇 |
2004年 | 165篇 |
2003年 | 123篇 |
2002年 | 113篇 |
2001年 | 103篇 |
2000年 | 110篇 |
1999年 | 87篇 |
1998年 | 82篇 |
1997年 | 68篇 |
1996年 | 40篇 |
1995年 | 40篇 |
1994年 | 26篇 |
1993年 | 21篇 |
1992年 | 11篇 |
1991年 | 9篇 |
1990年 | 10篇 |
1989年 | 6篇 |
1988年 | 16篇 |
1987年 | 3篇 |
1986年 | 15篇 |
1985年 | 15篇 |
1984年 | 9篇 |
1983年 | 3篇 |
1982年 | 8篇 |
1981年 | 8篇 |
1980年 | 1篇 |
排序方式: 共有4894条查询结果,搜索用时 15 毫秒
941.
塔里木盆地喀什凹陷克拉托天然气来源分析及聚气特征 总被引:2,自引:1,他引:1
塔里木西南喀什凹陷的克拉托天然气主要表现为原油的溶解气或者湿气,甲烷含量为74.59%~85.58%,克4井和克30井天然气则为较干的湿气。克拉托天然气的δ13C1值为-41.2‰~-40.6‰,δ13C2值为-30.0‰~-27.4‰。气源对比表明克拉托天然气主要源自具有混源母质特征的中侏罗统湖相烃源岩,不同于源自石炭系烃源岩的阿克莫木天然气。喀什凹陷的中-下侏罗统烃源岩主要是由于新近系的巨厚沉积才从未成熟—低成熟阶段进入成熟—高成熟阶段,生成的油气在克拉托背斜圈闭中聚集,虽也属晚期成藏,却具有连续聚气的特征。上新世末期,喀什凹陷的周缘开始抬升,早期油气藏受到破坏,形成了现今的地表油气苗或油砂。 相似文献
942.
利用重建的华南区域黑碳气溶胶(Black Carbon, BC)浓度资料,分析其与南海夏季风在年际尺度上的关系。结果表明,华南区域BC浓度与南海夏季风的关系在2000年前后有明显的突变,由显著负相关变为显著正相关,即由高BC浓度弱季风变为高BC浓度强季风。通过合成对比分析,发现1988—1999年(第一时间段)的华南BC主要气候效应是间接辐射强迫作用:华南BC使云粒子半径减小,抑制华南区域春季降水,增加了云的生命期,从而使到达地面的短波辐射减少,表面和低层大气降温。负温度异常激发了异常反气旋,在南海区域即有东风异常。到夏季,东风异常减弱了季风强度,同时抑制了南海地区的降水。2000—2010年(第二时间段)的华南BC主要气候效应是直接辐射强迫作用:春季高BC浓度通过直接气候效应,增暖大气,加强降水,但是雨日减少,从而使到达地面的短波辐射增多,表面和低层大气增温。正温度异常激发了异常气旋,在南海区域即有西风异常一直维持到夏季,增大了季风强度,同时增强了南海地区的降水。 相似文献
943.
有机碳和无机碳的流域输出是湖泊碳埋藏的重要驱动因子,而喀斯特地区无机碳循环具有反应迅速且对人类活动影响敏感的特点.在流域开发持续增强的背景下,喀斯特地区湖泊有机碳和无机碳的来源、含量与埋藏通量可能会出现同步变化的协同模式.本文以云南省石林喀斯特地区流域土地利用类型不同的两个中型湖泊(长湖、月湖)开展对比分析,通过对沉积物钻孔的土壤侵蚀强度(磁化率)、流域外源输入(C:N比值)、水动力(粒度)、营养盐(总氮、总磷)、藻类生产力(叶绿素色素)等代用指标的分析,结合监测数据和历史资料重建了两个湖泊环境变化的近百年历史,并定量识别了有机碳和无机碳埋藏响应流域开发的变化特征与协同模式.沉积物磁化率和C:N比值结果揭示了流域地表侵蚀和外源输入的阶段性特征,同时总氮和总磷含量记录了长湖和月湖营养水平上升的长期模式.在流域森林覆被较高(33.43%)的长湖中,全岩和有机质C:N比值分别与磁化率信号呈显著正相关(r=0.95和0.89,P<0.001),且与无机碳和有机碳含量呈显著负相关(r=-0.94,P<0.001和r=-0.52,P=0.01),反映了森林植被退化时流域碳输出的减少对沉... 相似文献
944.
Alluviation and sedimentation of the Yellow River are important factors influencing the surface soil structure and organic carbon content in its lower reaches. Selecting Kaifeng and Zhoukou as typical cases of the Yellow River flooding area, the field survey, soil sample collection, laboratory experiment and Geographic Information System(GIS) spatial analysis methods were applied to study the spatial distribution characteristics and change mechanism of organic carbon components at different soil depths. The results revealed that the soil total organic carbon(TOC), active organic carbon(AOC) and nonactive organic carbon(NOC) contents ranged from 0.05–30.03 g/kg, 0.01–8.86 g/kg and 0.02–23.36 g/kg, respectively. The TOC, AOC and NOC contents in the surface soil layer were obviously higher than those in the lower soil layer, and the sequence of the content and change range within a single layer was TOCNOCAOC. Geostatistical analysis indicated that the TOC, AOC and NOC contents were commonly influenced by structural and random factors, and the influence magnitudes of these two factors were similar. The overall spatial trends of TOC, AOC and NOC remained relatively consistent from the 0–20 cm layer to the 20–100 cm layer, and the transition between high-and low-value areas was obvious, while the spatial variance was high. The AOC and NOC contents and spatial distribution better reflected TOC spatial variation and carbon accumulation areas. The distribution and depth of the sediment, agricultural land-use type, cropping system, fertilization method, tillage process and cultivation history were the main factors impacting the spatial variation in the soil organic carbon(SOC) components. Therefore, increasing the organic matter content, straw return, applying organic manure, adding exogenous particulate matter and conservation tillage are effective measures to improve the soil quality and attain sustainable agricultural development in the alluvial/sedimentary zone of the Yellow River. 相似文献
945.
946.
947.
The flux of fluvial carbon from the terrestrial biosphere to the world's oceans is known to be an important component of the global carbon cycle, but within this pathway, the flux and return of carbon to the river network via sewage effluent has not been quantified. In this study, monitoring data from 2000 to 2016 for the dissolved organic carbon (DOC) concentration, biochemical oxygen demand, and chemical oxygen demand of the final effluent of sewage treatment works from across England were examined to assess the amount of DOC contributing to national‐scale fluvial fluxes of carbon. The study shows that the median concentration of DOC in final effluent was 9.4 compared with 4.8 mg C/L for all surface waters for the United Kingdom over the study period and that the DOC in final effluent significantly declined over the study period from 11.0 to 6.4 mg C/L. Rivers receiving sewage effluent showed a significant, on average 19%, increase in DOC concentration downstream of sewage discharges. At the scale of the United Kingdom, the flux of DOC in final effluent was 31 ktonnes C/year with a per capita export of 0.55 kg C/year and compared with an average annual flux of DOC from the United Kingdom of 859 ktonnes C/year, that is, only 3.6% of national‐scale flux. The lability of this DOC was limited, with only 7.4% loss of final effluent DOC concentration over in‐stream residence times of up to 5 days. The direct decline in DOC concentration from sewage treatment works was not large enough on its own to explain the declines observed in DOC concentration in U.K. rivers at their tidal limit. 相似文献
948.
Manuel D. Menzel Carlos J. Garrido Vicente Lpez Snchez‐Vizcaíno Kroly Hidas Claudio Marchesi 《Journal of Metamorphic Geology》2019,37(5):681-715
At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO2 contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO2 ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H2O–CO2 fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H2O and molecular CO2 are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H2O–CO2 fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle. 相似文献
949.
Kyle S. Boodoo Jakob Schelker Nico Trauth Tom J. Battin Christian Schmidt 《水文研究》2019,33(17):2279-2299
Gravel bars (GBs) contribute to carbon dioxide (CO2) emissions from stream corridors, with CO2 concentrations and emissions dependent on prevailing hydraulic, biochemical, and physicochemical conditions. We investigated CO2 concentrations and fluxes across a GB in a prealpine stream over three different discharge‐temperature conditions. By combining field data with a reactive transport groundwater model, we were able to differentiate the most relevant hydrological and biogeochemical processes contributing to CO2 dynamics. GB CO2 concentrations showed significant spatial and temporal variability and were highest under the lowest flow and highest temperature conditions. Further, observed GB surface CO2 evasion fluxes, measured CO2 concentrations, and modelled aerobic respiration were highest at the tail of the GB over all conditions. Modelled CO2 transport via streamwater downwelling contributed the largest fraction of the measured GB CO2 concentrations (31% to 48%). This contribution increased its relative share at higher discharges as a result of a decrease in other sources. Also, it decreased from the GB head to tail across all discharge‐temperature conditions. Aerobic respiration accounted for 17% to 36% of measured surface CO2 concentrations. Zoobenthic respiration was estimated to contribute between 4% and 8%, and direct groundwater CO2 inputs 1% to 23%. Unexplained residuals accounted for 6% to 37% of the observed CO2 concentrations at the GB surface. Overall, we highlight the dynamic role of subsurface aerobic respiration as a driver of spatial and temporal variability of CO2 concentrations and evasion fluxes from a GB. As hydrological regimes in prealpine streams are predicted to change following climatic change, we propose that warming temperatures combined with extended periods of low flow will lead to increased CO2 release via enhanced aerobic respiration in newly exposed GBs in prealpine stream corridors. 相似文献
950.
Coastal peatlands represent an interface between marine and terrestrial ecosystems; their hydrology is affected by salt and fresh water inflow alike. Previous studies on bog peat have shown that pore water salinity can have an impact on the saturated hydraulic conductivity (Ks) of peat because of chemical pore dilation effects. In this study, we aimed at quantifying the impact of higher salinities (up to 3.5% NaCl) on Ks of fen peat. Two experiments employing a constant‐head upward‐flow permeameter and differing in measurement and salinity change duration were conducted. Additionally, a third experiment to determine the impact of water salinity on the release of dissolved organic carbon (DOC) of the studied peat type was carried out. The results show a decrease of Ks with time, which does not depend on the water salinity but is differently shaped for different peat types. We assume pore clogging due to a conglomerate of physical, chemical, and biological processes, which rather depend on water movement rate and time than on water salinity. However, an increased water salinity did increase the DOC release. We conclude that salinity‐dependent behaviour of Ks is a function of peat chemistry and that for some peat types, salinity may only affect the DOC release without having a pronounced impact on water flow. 相似文献