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161.
In arctic and sub‐arctic environments, mercury (Hg), more specifically toxic methylmercury (MeHg), is of growing concern to local communities because of its accumulation in fish. In these regions, there is particular interest in the potential mobilization of atmospherically deposited Hg sequestered in permafrost that is thawing at unprecedented rates. Permafrost thaw and the resulting ground surface subsidence transforms forested peat plateaus into treeless and permafrost‐free thermokarst wetlands where inorganic Hg released from the thawed permafrost and draining from the surrounding peat plateaus may be transformed to MeHg. This study begins to characterize the spatial distribution of MeHg in a peat plateau–thermokarst wetland complex, a feature that prevails throughout the wetland‐dominated southern margin of thawing discontinuous permafrost in Canada's Northwest Territories. We measured pore water total Hg, MeHg, dissolved organic matter characteristics and general water chemistry parameters to evaluate the role of permafrost thaw on the pattern of water chemistry. A gradient in vegetation composition, water chemistry and dissolved organic matter characteristics followed a toposequence from the ombrotrophic bogs near the crest of the complex to poor fens at its downslope margins. We found that pore waters in poor fens contained elevated levels of MeHg, and the water draining from these features had dissolved MeHg concentrations 4.5 to 14.5 times higher than the water draining from the bogs. It was determined through analysis of historical aerial images that the poor fens in the toposequence had formed relatively recently (early 1970s) as a result of permafrost thaw. Differences between the fens and bogs are likely to be a result of their differences in groundwater function, and this suggests that permafrost thaw in this landscape can result in hotspots for Hg methylation that are hydrologically connected to downstream ecosystems. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   
162.
中国北方干旱/半干旱区是全球主要的沙尘源区之一,风蚀造成的沙尘排放可导致大量的土壤有机质(SOM)与养分流失,并通过传输与沉降过程对其进行空间再分配,对空气质量、气候变化、植被生长及生物地球化学过程等具有重要影响。本文利用WRF/Chem(Weather Research Forecasting with Chemistry)v3.7.1大气化学传输模型,对1980—2015年间中国北方沙尘排放及其引起的SOM、全氮(TN)与全磷(TP)的时空变化过程进行了精细化模拟,探究了中国北方风蚀引起的SOM、TN与TP养分流失的时空变化特征。结果表明:① 1980—2015年来平均每年约有66.59 Tg的沙尘颗粒排放至大气;② 沙尘排放具有较大的时空差异,沙尘排放源区主要集中在新疆东部、内蒙古西部的巴丹吉林沙漠和腾格里沙漠等地区;③ 每年因沙尘排放引起的SOM、TN和TP流失量分别约为0.07 Tg、0.004 Tg和0.005 Tg;④ 1980—2015年间中国北方沙尘排放及其引起的SOM、TN与TP的流失量具有较强的年际波动,未呈现显著的趋势性变化特征。本研究对于认知风蚀在碳循环与养分循环过程中的作用,以及对深入了解中国北方的土地退化机理具有重要意义。  相似文献   
163.
Located between terrestrial and marine ecosystems, mangrove forests are sensitive to changes in climate. The responses of mangrove ecosystems to climate change in the future can be understood by reconstructing past mangrove dynamics using proxies preserved in the intertidal sediments. Considering the complexity of the proxies commonly used, it is necessary to develop a relatively simple, inexpensive proxy. In this study, available chemical tracers (δ13Corg and C:N) of the four cores (YLW02, YLW03, O18, and Q37) from the intertidal zone of the northern Beibu Gulf (NBG) and a three-end-member (mangrove, sea grass, and suspended particulate matter) model was utilized to determine the contribution of mangrove-derived organic matter (CMOM) in carbonate-free sediments. Compared with the summed concentration of mangrove pollen (SCMP), a significant positive correlation between CMOM and SCMP is displayed. The calculated CMOM for an additional 210Pb-dated sediment core from the Yingluo Bay, NBG (YLW01) clearly indicates a mangrove development going through degradation, flourishing, relative degradation, and relative flourishing, which are separately in correspondence with the lowest, highest, lower, and higher air temperature and rainfall in the time intervals of 1890–1918 AD, 1919–1956 AD, 1957–1990 AD, and 1991–2010 AD. This suggests that CMOM preserved in intertidal sediments has a potential to reconstruct historical mangrove development in high resolution, at the very least, along the coasts of the NBG.  相似文献   
164.
On 25th January 2019, the tailings dam of the Brumadinho iron mine operated by Vale S/A failed catastrophically. The death toll stood at 259 and 11 people remained missing as of January 2020. This tragedy occurred three years after Mariana’s tailings dam rupture – the most significant tailing dam disaster in Brazilian history. Thus far, a systematic investigation on the cause and effect of the failure has yet to be conducted. Here, we use satellite-driven soil moisture index, multispectral high-resolution imagery and Interferometric Synthetic Aperture Radar (InSAR) products to assess pre-disaster scenarios and the direct causes of the tailings dam collapse. A decreasing trend in the moisture content at the surface and the full evanescence of pond water through time (2011–2019) suggest that the water was gradually penetrating the fill downwards and caused the seepage erosion, saturating the tailings dam. Large-scale slumping of the dam (extensional failure) upon the rupture indicates that the materials of the fill were already saturated. InSAR measurements reveal a dramatic, up to 30 cm subsidence in the dam (at the rear part) within the past 12 months before the dam collapse, signifying that the sediments had been removed from the fill. Although the information on the resistance level of the tailings dam to infiltrations is not available, these pieces of evidence collectively indicate that the seepage erosion (piping) is the primary cause for the chronic weakening of the structure and, hence, the internal “liquefaction” condition. Upon the collapse, the fully saturated mud tailings flowed down the gentle slope area (3.13 × 106 m2), where 73 % were originally covered by tree, grass or agricultural tracts. The toxic mud eventually reached the Paraopeba River after travelling 10 km, abruptly increasing the suspended particulate matter (SPM) concentration and the toxic chemical elements in the river, immediately affecting the local livelihoods that depend on its water. The Paraopeba River is a major tributary of the San Francisco River, the second-longest river in Brazil reaching the Atlantic Ocean. We anticipate that the environmental repercussions of this toxic seepage will be felt throughout the entire basin, especially riverine communities located downstream.  相似文献   
165.
Many of the commonly used analytical techniques for assessing the properties of fluvial suspended particulate matter (SPM) are neither cost effective nor time efficient, making them prohibitive to long‐term high‐resolution monitoring. We present an in‐depth methodology utilizing two types of spectroscopy which, when combined with automatic water samplers, can generate accurate, high‐temporal resolution SPM geochemistry data, inexpensively and semi‐destructively, directly from sediment covered filter papers. A combined X‐ray fluorescence spectroscopy and diffuse reflectance infrared Fourier transform spectroscopy approach is developed to estimate concentrations for a range of elements (Al, Ca, Ce, Fe, K, Mg, Mn, Na, P, Si, Ti) and compounds (organic carbon, Aldithionate, Aloxalate, Fedithionate, and Feoxalate) within SPM trapped on quartz fibre filters at masses as low as 3 mg. Calibration models with small prediction errors are derived, along with mass correction factor models to account for variations in retained SPM mass. Spectral pre‐processing methods are shown to enhance the reproducibility of results for some compounds, and the importance of filter paper selection and homogeneous sample preparation in minimizing spectral interference is emphasized. The geochemical signal from sediment covered filter papers is demonstrated to be time stable enabling samples to be stored for several weeks prior to analysis. Example results obtained during a heavy precipitation event in October 2012 demonstrate the methodology presented here has considerable potential to be utilized for high‐resolution monitoring of SPM geochemistry under a range of in‐stream hydrological conditions. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
166.
Exploring the chemical characterization of dissolved organic matter (DOM) is important for understanding the fate of laterally transported organic matter in watersheds. We hypothesized that differences in water-extractable organic matter (WEOM) in soils of varying land uses and rainfall events may significantly affect the quality and the quantity of stream DOM. To test our hypotheses, characteristics of rainfall-runoff DOM and WEOM of source materials (topsoil from different land uses and gullies, as well as typical vegetation) were investigated at two adjacent catchments in the Loess Plateau of China, using ultraviolet–visible absorbance and excitation emission matrix fluorescence with parallel factor analysis (PARAFAC). Results indicated that land-use types may significantly affect the chemical composition of soil WEOM, including its aromaticity, molecular weight, and degree of humification. The PARAFAC analysis demonstrated that the soils and stream water were dominated by terrestrial/allochthonous humic-like substances and microbial transformable humic-like fluorophores. Shifts in the fluorescence properties of stream DOM suggested a pronounced change in the relative proportion of allochthonous versus autochthonous material under different rainfall patterns and land uses. For example, high proportions of forestland could provide more allochthonous DOM input. This study highlights the relevance of soils and hydrological dynamics on the composition and fluxes of DOM issuing from watersheds. The composition of DOM in soils was influenced by land-use type. Precipitation patterns influenced the proportion of terrestrial versus microbial origins of DOM in surface runoff. Contributions of allochthonous, terrestrially derived DOM inputs were highest from forested landscapes.  相似文献   
167.
根据2017年7月和9月在山东威海褚岛北部海域现场测量的COD_(Mn)(Chemical oxygen demand)值和水体表观光学量,结合COMS(Communication,OceanMeteorological Satellite)上搭载的传感器GOCI(Geostationary Ocean Color Imager)所提供的有色可溶性有机物(Chromophoric dissolved organic matter,CDOM)产品,利用星地同步观测数据对现有的基于遥感反射比反演CDOM的模式进行验证,确定适合该海域的CDOM浓度遥感反演模式;通过对测试海域化学需氧量与遥感反演的水体CDOM浓度相关性分析,建立利用CDOM反演COD_(Mn)的遥感模式,并将该模式应用于测试海域LANDSAT 8/OLI(Operational Land Imager)遥感图像上,获取该海域COD_(Mn)浓度专题图,基于这些专题图分析了测试海域COD_(Mn)时空分布特征。结果表明:(1)基于GOCI产品的CDOM浓度值随时间和站点动态变化大,离岸越近数值越高,同一地点水体前后相差近1 h的数值变化也较大;(2)基于LANDSAT 8/OLI遥感数据反演的COD_(Mn)浓度时间动态变化大,总体来看褚岛附近水体的COD_(Mn)含量相对较低,褚岛以北海域水体COD_(Mn)含量有所增加,褚岛西侧水体的COD_(Mn)含量较东侧水体COD_(Mn)含量来说整体偏高。  相似文献   
168.
硅微条探测器具有位置分辨高、响应快、低噪声、低功耗等优点,广泛应用在各大加速器试验中,测量粒子径迹.新世纪以来,逐渐应用于空间探测领域.计划中的"悟空"2号暗物质粒子探测卫星的硅微条探测器将至数十万计,将产生海量的原始数据.如何实现探测器快速实时的数据压缩,是其需要解决的一大难题.立足于面向空间应用的硅微条探测器在轨实时压缩算法,算法采用FPGA (Field-programmable Gate Array)搭建流水线结构的方式实现,在提高系统集成度、节省逻辑资源的同时,批量数据处理时最高可将数据压缩率提升至38.4 M通道/s.算法结构具有通用性,设计思想和方案将为"悟空"2号的径迹探测器的研制提供参考.  相似文献   
169.
与搭载气溶胶观测和分析仪器测量相比,利用无人直升机搭载气囊采集高空大气颗粒物是一种经济、便捷和安全的采集方式。为了解无人直升机采样装置的采样效果,选择2014年10月至2015年3月的4次重污染天气过程,由无人直升机搭载气囊采集大气颗粒物,然后利用气溶胶采样器采集气囊内的大气颗粒物样品并计算采样时间,再利用气溶胶采样器采集相同时间段内的地面大气颗粒物(气囊外),并将两者进行对比。结果表明:在稳定的污染天气条件下,采集气囊内的大气颗粒物,与相同时间段内利用气溶胶采样器直接采集气囊外的大气颗粒物相比,两种方式采集到的大气颗粒物质量最大差值29%,最小差值11%,平均为21%;利用无人直升机的大气采样装置采集大气颗粒物对碳气溶胶组分影响很小,气囊内与气囊外OC/TC最大相差2.0%,最小相差0.5%。上述结果表明,无人直升机的大气采样装置有比较好的采集效率,利用气囊这种经济、便捷、安全的方式,搭载在无人机平台上,采集高空大气是一种获取气溶胶垂直廓线的有效方法,有望在未来的气溶胶气候和环境研究中提供宝贵数据。  相似文献   
170.
鄂尔多斯盆地北部直罗组有机质特征及与铀成矿关系   总被引:2,自引:0,他引:2  
本文研究了鄂尔多斯盆地典型铀矿床的有机质与铀成矿的关系。探讨了煤屑的赋存状态、煤质特征及成熟度,认为煤屑的演化程度均较低,处于低成熟阶段,有利于对铀的吸附。总体上看煤质有机质和铀矿化关系密切,铀含量与煤屑含量呈正相关关系,对铀矿物为吸附态形式。通过对该区油气包裹体的研究认为,该区存在多期次的成岩方解石胶结过程,并伴随多期次的油气包裹体发育,尤以晚期的胶结方解石矿物中存在丰富的晚期油气包裹体。研究认为晚期可能发生过油、气的运移和聚集,铀矿床的形成与赋矿砂岩中有机流体或还原性气体的充注和络合作用密切相关,因而这些丰富的有机流体和还原性气体对于铀的富集沉淀具有重要意义。  相似文献   
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