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941.
Recent studies have found insignificant or decreasing trends in time‐series dissolved organic carbon (DOC) datasets, questioning the assumption that long‐term DOC concentrations in surface waters are increasing in response to anthropogenic forcing, including climate change, land use, and atmospheric acid deposition. We used the weighted regressions on time, discharge, and season (WRTDS) model to estimate annual flow‐normalized concentrations and fluxes to determine if changes in DOC quantity and quality signal anthropogenic forcing at 10 locations in the Mississippi River Basin. Despite increases in agriculture and urban development throughout the basin, net increases in DOC concentration and flux were significant at only 3 of 10 sites from 1997 to 2013 and ranged between ?3.5% to +18% and ?0.1 to 19%, respectively. Positive shifts in DOC quality, characterized by increasing specific ultraviolet absorbance at 254 nm, ranged between +8% and +45%, but only occurred at one of the sites with significant DOC quantity increases. Basinwide reductions in atmospheric sulfate deposition did not result in large increases in DOC either, likely because of the high buffering capacity of the soil. Hydroclimatic factors including annual discharge, precipitation, and temperature did not significantly change during the 17‐year timespan of this study, which contrasts with results from previous studies showing significant increases in precipitation and discharge over a century time scale. Our study also contrasts with those from smaller catchments, which have shown stronger DOC responses to climate, land use, and acidic deposition. This temporal and spatial analysis indicated that there was a potential change in DOC sources in the Mississippi River Basin between 1997 and 2013. However, the overall magnitude of DOC trends was not large, and the pattern in quantity and quality increases for the 10 study sites was not consistent throughout the basin.  相似文献   
942.
黔中小流域水体C、S同位素特征及主要风化过程   总被引:1,自引:0,他引:1  
选取贵州省红枫湖流域四条支流为研究对象,通过对水体中C、S元素浓度及稳定同位素特征的分析,探讨了典型碳酸盐小流域的主要风化过程对流域C、S循环的贡献。红枫湖流域河水中的C同位素组成在-7.47‰--11.68‰之间,硫酸根浓度为295.5~1315.6μmol/L,除受当地煤矿影响较大的区域外,其余部分水体中离子的δ^34S值在-3‰--7‰之内,反映了这些河段中硫化物矿物的氧化的影响。通过质量守恒的方法,得到硫化物的氧化、蒸发岩溶解以及大气输入对河水硫酸根离子的贡献率分别为63.8%、30.8%和5.4%。来自硫酸对碳酸盐岩、碳酸对碳酸盐岩以及碳酸对硅酸盐岩风化的DIC比例为1:3.58:1.37,三种不同的风化过程对区域二氧化碳的净吸收量为7.97×10^9mol/a。  相似文献   
943.
赵敏  曾成  刘再华 《地球化学》2009,38(6):565-572
土地利用变化对岩溶地下水溶解无机碳(DIC)的影响关系到岩溶作用强弱及其相关的全球碳循环的正确评价。对贵州茂兰原始森林内的板寨岩溶地下河流域和普定岩溶石漠化强烈的陈旗、灯盏河泉域三种不同的土地利用下的地下水的DIC及其稳定同位素进行了分析,结果表明,地下水的DIC表现形式主要为HCO3^-。对于缺少土壤覆盖的板寨和灯盏河岩溶地区,雨季主要因为稀释作用,HCO3^-含量出现年内最低值;而对于较多土壤覆盖的陈旗岩溶地区,雨季主要受土壤CO2效应控制。HCO3^-含量出现年内最高值,反映了土壤在岩溶作用及其碳循环中的特殊重要性。此外,夏季由于生物量的增加,δ^13DIC值较冬季偏轻1‰~2‰。而对于不同土地利用而言,石漠化影响下的地下水δ^13DIC较原始森林下的地下水偏重2.5‰-3.0‰,且随着石漠化的发展,土壤的进一步流失,地下水δ^13DIC进一步偏重,反映了石漠化后生物量比例减少和大气成因CO2比例增加对地下水δ^13DIC升高的影响。  相似文献   
944.
Changes in the hydrologic characters of the Tarim River Basin of Xinjiang Province during the past 50 years were studied to identify the key factors responsible for these changes. Observed hydrologic and socio-economic data provided the basis for this study. The impact of human activities on the decrease in the streamflow and changes in total dissolved solids (TDS) in the watercourse and groundwater of the mainstream were analyzed using the Mann–Kendall test, regression and principal component analysis. The results showed that during the past 50 years the streamflow in the headwater streams has increased slightly while the streamflow in the mainstream has decreased significantly. Human activities along the mainstream are the primary reason for the decreased streamflow, with the impact of human activities on the decrease in the streamflow of the mainstream being 65.61, 74.73 and 77.62% in the 1970s, 1980s and 1990s, respectively. The key factor that affected the TDS of the watercourse was the decreasing streamflow, which was caused by anthropological activities. However, the TDS of the groundwater was found to be affected significantly by groundwater depth. The degeneration of ecosystems in the lower reaches of the Tarim River was directly related with anthropogenic activities.  相似文献   
945.
利用陶瓷头土壤溶液收集器采集2006年7月~2007年8月问长白山阔叶红松天然林不同深度(15cm和60 cm)土壤溶液,探讨应用气液萃取平衡-气相色谱法测定森林土壤溶液中溶解性气体N_2O和CO_2浓度的可行性,并利用此方法研究林地不同深度土壤溶液中两种气体含量特征及其影响机理.研究结果显示观测期内林地15 cm和60 cm深度土壤溶液中溶解性CO_2浓度的变化范围分别为5.26~10.71μg·mL~(-1)(C)和3.13~6.16 μg·mL~(-1)(C),溶解性N_2O浓度的变化范围分别为2.44~13.40 ng·mL~(-1)(N)和3.23~27.98 ng·mL~(-1)(N).阔叶红松天然林土壤溶液中溶解性CO_2和N_2O浓度均呈现出明显的季节性变化.春融后的降水促进了土壤溶液中溶解性N_2O产生,尤其在60 cm深度.与60 cm深度相比,林地15 cm深度溶液中溶解性CO_2浓度的季节性变化更明显,尤其在植物生长旺季.逐步回归分析显示,水溶性有机碳含量可以解释林地不同深度溶液中溶解性CO_2浓度变化的29%;水溶性有机氮含量可以解释林地60 cm深度溶解性N_2O浓度变化的34%.因此,水溶性有机碳和有机氮分别是长白山阔叶红松林土壤溶液溶解性CO_2和N_2O形成的重要因子.同时研究结果表明本文实验方法对于测定林地不同深度土壤溶液中溶解性N_2O和CO_2含量均有较好的适用性,连续三次萃取后所获得的气体浓度可有效反映溶液中的实际气体浓度.  相似文献   
946.
高温硅酸盐熔体粘度与网络分数维值的相关性研究   总被引:1,自引:0,他引:1  
对高温硅酸盐熔体粘度的估算一直是国际地学界热点问题之一,本文在研究了高温硅酸盐熔体网络分数维值的基础上,建立了估算熔体粘度的新模式 (简称 FD模式 ) ,阐明了熔体粘度值除了与温度成反比外,还与分子网络介观尺度的自相似比 ri 和分数维值 D相关,即与分子网络 (纳米尺度以上 )中的桥氧数 Ni成正比 (Ni∝ ) , 与单位硅氧四面体中的非桥氧数成反比.经对 4个硅酸盐系列高温熔体的粘度测定证实, FD模式的理论计算值与实测值吻合,且优于现今国际通用的 VTF模式.为探索岩浆迁移演化规律和完善新型低维材料的性能提供了新的理论依据.  相似文献   
947.
The Nyangqu River, the largest right bank tributary of the Yarlung Zangbo River in the Qinghai–Tibet Plateau, was representative of an alpine riverine carbon cycle experiencing climate change. In this study, dissolved inorganic carbon (DIC) spatial and seasonal variations, as well as their carbon isotopic compositions (δ13CDIC) in river water and groundwater were systematically investigated to provide constraints on DIC sources, recharge and cycling. Significant changes in the δ13CDIC values (from −2.9‰ to −23.4‰) of the water samples were considered to be the result of different contributions of two dominant DIC origins: soil CO2 dissolution and carbonate weathering. Three types of rock weathering (dissolution of carbonate minerals by H2CO3 and H2SO4, and silicate dissolution by H2CO3) were found to control the DIC input into the riverine system. In DIC cycling, groundwater played a significant role in delivering DIC to the surface water, and DIC supply from tributaries to the main stream increased from the dry season to the wet season. Notably, the depleted δ13CDIC ‘peak’ around the 88.9° longitude, especially in the September groundwater samples, indicated the presence of ‘special’ DIC, which was attributed to the oxidation of methane from the Jiangsa wetland located nearby. This wetland could provide large amounts of soil organic matter available for bacterial degradation, producing 13C-depleted methane. Our study provided insights regarding the role of wetlands in riverine carbon cycles and highlighted the contribution of groundwater to alpine riverine DIC cycles.  相似文献   
948.
This study investigated CO2 degassing and related carbon isotope fractionation effects in the Wiesent River that drains a catchment in the karst terrain of the Franconian Alb, Southern Germany. The river was investigated by physico‐chemical and stable isotope analyses of water and dissolved inorganic carbon during all seasons along 65‐km long downstream transects between source and mouth. Calculated pCO2 values at the source were 21 400 ± 2400 µatm. The pCO2 rapidly decreased in the river water and dropped to an average of 1240 ± 330 µatm near the mouth. About 90% of this decrease occurred within the first 6 km of the river. The river was supersaturated with respect to CO2 over its entire course and must have acted as a continuous year‐round CO2 source to the atmosphere. The average CO2 flux from the karst river was estimated with 450 mmol m?2 day?1 with higher fluxes up to 5680 mmol m?2 day?1 at the source. At the source, δ13CDIC values showed no seasonal variations with an average of ?14.2 ± 0.2‰. This indicated that groundwater retained high pCO2 mainly from soil CO2. The contribution of soil CO2 to dissolved inorganic carbon was estimated at 65% to 72%. The downstream CO2 loss caused a positive shift in δ13CDIC values of 2‰ between source and mouth because of the preferential loss of the 12C isotope during degassing. Considering the findings of this study and the fact that carbonate lithology covers a significant part of the earth's surface, CO2 evasion from karst regions might contribute notably to the annual carbon dioxide release from global freshwater systems. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   
949.
Synoptic water sampling at a fixed site monitoring station provides only limited ‘snap‐shots’ of the complex water quality dynamics within a surface water system. However, water quality often changes rapidly in both spatial and temporal dimensions, especially in highly polluted urban rivers. In this study, we designed and applied a continuous longitudinal sampling technique to monitor the fine‐scale spatial changes of water quality conditions, assess water pollutant sources, and determine the assimilative capacity for biochemical oxygen demand (BOD) in an urban segment of the hypoxic Wen‐Rui Tang River in eastern China. The continuous longitudinal sampling was capable of collecting dissolved oxygen (DO) data every 5 s yielding a ~11 m sampling interval with a precision of ±0.1 mg L?1. The Streeter and Phelps BOD‐DO model was used to calculate: (1) the oxygen consumption coefficient (K1) required for calibration of water quality models, (2) BOD assimilative capacity, and (3) BOD source and load identification. In the 2014 m river segment sampled, the oxygen consumption coefficient (K1) was 0.428 d?1 (20°C), the total BOD discharge was 916 kg d?1, and the BOD assimilative capacity was 382 kg d?1 when the minimum DO level was set to 2 mg L?1. In addition, the longitudinal analysis identified eight major drainage outlets (BOD point sources), which were verified by field observations. This new approach provides a simple, cost‐effective method of evaluating BOD‐DO dynamics over large spatial areas with rapidly changing water quality conditions, such as urban environments. It represents a major breakthrough in the development and application of water quality sampling techniques to obtain spatially distributed DO and BOD in real time. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
950.
Boreal mire landscapes are rich in soil carbon and significantly contribute to the carbon input of aquatic ecosystems. They are composed of different mesoscale ecohydrological subunits, whose individual contributions to the water and carbon export of mire catchments are not well understood. The spring snowmelt period is the major hydrological event in the annual water cycle of the boreal regions and strongly influences the carbon flux between the terrestrial and aquatic systems. The aim of this study was (1) to provide a conceptual understanding of the spatial and temporal dynamics of the surface water chemistry along a swamp forest‐fen‐bog gradient during the snowmelt period, (2) to quantify the exported dissolved organic carbon (DOC) content in the runoff and (3) to identify the ecohydrological landscape unit that contributes most to DOC export during the snowmelt period in a heterogeneous mire complex in Northwest Russia. The highest DOC concentrations were detected in the swamp forest, and the lowest concentrations were observed at the treeless bog by the end of the snowmelt period (swamp forest: 37–43 mg l?1, bog: 13–17 mg l?1). During the spring snowmelt period, a significant amount (~1.7 g C m?2) of DOC was transferred by the ~74 mm of runoff from the catchment into the river. Variability in the thawing periods led to differences in the relative contributions of each ecohydrological zone to the carbon export measured at a stream channel draining the studied part of the mire complex. An increased understanding of the variation in DOC concentrations and contributions from the mesoscale ecohydrological subunits to carbon export can help to predict the potential regional loss of DOC based on land cover type under climate change. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   
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