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61.
A large body of existing theories of flow and contaminant transport in aquifers ignore the presence of recharge, eliminate the boundary conditions, neglect transient conditions in groundwater flow, conceive hydraulic gradients as linear, and require parameter variability to be stationary and Gaussian. The most outstanding and difficult to justify assumption is the subjective small size of the stochastic terms (i.e., small perturbation methods), which usually is forced by considering the logarithm of the hydraulic conductivity. Several problems in flow and contaminant subsurface hydrology, such as the enhanced dispersion parameters with plume size or time after injection, remain to be observed in the light of a stochastic theory that allows a more realistic consideration of physical and hydrologic properties. In this article, an attempt is made to reformulate a contaminant transport equation (the variable dispersion equation, VDE) with transport parameters in terms of regional hydrologic and aquifer hydraulic properties, such as recharge rate, spatially random transmissivity, hydraulic gradient, aquifer thickness, and soil porosity. Subsequently, a general analytic procedure, the method of decomposition, is used to derive a solution to the VDE. This procedure does not require small perturbation, logarithmic transformations, or specific probability law assumptions. Comparison tests with existing theoretical and field results are given. The tests illustrate the enhanced dispersion and shifting concentration effects produced by the variable dispersion equation. Finally a generalization of the method to nonstationary dispersion in three-dimensional domains is proposed.  相似文献   
62.
Heavy rainfall and dense vegetation on tropical volcanoes produce abundant carbonized wood in pyroclastic deposits, in addition to easy contamination of this wood by root systems and soluble humic material. Because the physical nature of the charcoal varies, some samples are more prone to contamination. Two independent studies of the same volcano, Mt Liamuiga on St Kitts in the Lesser Antilles, sometimes using samples from the same carbonized tree, yielded a systematic difference in radiocarbon ages. An exchange of samples and a re-investigation of three physically distinct types of charcoal yielded the following results. Rare, hard, dense charcoal, lacking contamination, which had yielded a spurious age of 2860 years bp, was redated at 1845±58 years bp. Common soft, friable charcoal with good cellular structure proved to be susceptible to contamination. A field decontamination technique utilized by one group seems significant as it yields older ages than when only routine laboratory pre-treatment was used, indicating that the latter technique only partly removes the dried and hard residue produced by the decomposition of modern plant rootlets. A previous date of 24870 years bp obtained from powdery charcoal in a horizon beneath the Mansion Series contradicted ages older than 41000 years bp from common friable charcoal in the lower Mansion Series. The soft powdery charcoal was re-investigated using a sample collected a few centimeters from the original, although field decontamination of this sample was not possible, more extensive laboratory treatment yielded an age of ca. 43000 years bp, again proving that routine laboratory pretreatments are inadequate. A revised geochronology for the Mansion Series is described and a cautionary discussion is presented for the benefit of investigators using radiocarbon ages to date volcanic deposits.  相似文献   
63.
分析了浅埋藏砂岩的成岩环境,并从岩石学、矿物学、同位素及质量平衡估算方面论证硅质碎屑砂岩中的胶结物主要来源于砂岩浅埋藏期间的地下水,进而分析浅埋藏带内地下水的流动机制及早期胶结作用对晚期成岩作用的影响。  相似文献   
64.
Prototype instrumentation, able to automatically measure groundwater radon content variations, is presented. The equipment is made of stainless steel and has spherical valves with automatic and pneumatic control. The deemanation of the gases from the water is obtained by evacuating a suitable expansion chamber. The instrumentation can make discrete sampling ranging from 1 per hour to 1 per 99 hours. The equipment was tested in the laboratory: the efficiency was measured by means of a266Ra solution. A mean value of (0.65±0.07) count/s/Bq was obtained. A calibration test was carried out by comparing countings from the automatic equipment with those obtained by the standard laboratory cell. Results of an operational check over a period of approximately one year indicate that variations in radon at the calibration site are attributable more to meteorological than to tectonic causes.  相似文献   
65.
渗流域内应用拉普拉斯变换(LT)建立相应的有限分析(FAM)方程,顾及渗流域内地下水流的初始条件和边界条件,可在LT空间构成一个封闭的以水头像函数为变量的线性方程组。将此方程组所得的解,通过Stehfest数值反演公式,可归化为时间域的解(水头)。由于时间t被隐含在数值方程内,从而克服了传统数值法按时段(△t)逐步迭代的缺陷,提高了计算效率,也为用嵌入法建立地下水流管理模型提供了一条捷径。  相似文献   
66.
为了定量计算陵区近海核电站排水管线泄漏情景下核素通过地下水途径向海洋环境的释放通量,以某近海核电站为例进行研究。首先,应用GOCAD软件建立三维地形地质模型,刻画地层的分布、剥蚀以及倾向等特点;然后,运用地下水数值模拟软件FEFLOW精细刻画丘陵区地下水系统的补给、径流和排泄特征;最后,以不被吸附滞留的核素3H和被吸附滞留的核素90Sr、137Cs为对象,通过实验测定了90Sr、137Cs在不同岩土介质中的分配系数,模拟计算了排水管线连续渗漏60 a后3H、90Sr、137Cs在地下水中的放射性分布及释放。结果表明:3H迁移速度基本与地下水流速一致,地下水中的最大放射性浓度为0.285 0 Bq/L,第20 000天时向收纳水域的释放通量达到最大值,约526 Bq/d;90Sr吸附性能相对较弱,最大迁移距离约80 m,地下水中的最大放射性浓度为0.032 1 Bq/L;137Cs吸附能力较强,相当长的时间内被滞留在管线附近,地下水中最大放射性浓度分别为6.840×10-3 Bq/L,释放通量为0 Bq/d。由弥散度的不确定分析可知,弥散度越大,地下水中3H的最大放射性浓度越小,向海洋环境的释放通量越多。  相似文献   
67.
地下水中高浓度的铵态氮对生活饮用水安全及生态环境存在潜在威胁。相比较硝态氮,高浓度的铵态氮不仅有各种人为来源,天然沉积环境更是造成高铵地下水的主要成因。本文以城镇化快速发展的珠江三角洲为研究区,运用数理统计、主成分分析等方法深入探讨了研究区高铵地下水的赋存环境特征及驱动因素。结果表明,研究区地下水中NH4+质量浓度介于未检出~180 mg/L。研究区1539组地下水样品中,NH4+质量浓度大于10 mg/L的高铵地下水69组,其中含NH4+质量浓度大于30 mg/L的高铵"肥水"23组。对比2005-2008年历史水化学数据,2009-2018年新增建设用地孔隙含水层高铵地下水样品比例增加25%。高铵地下水呈斑块状分布于三角洲平原区第四系底部低洼的基底、洼地等退积层序发育的淤泥质含水层中。淤泥层等富含有机质和总有机碳的沉积层是珠江三角洲地区的"生铵层",有机氮的矿化是三角洲平原区城市化孔隙含水层中高铵地下水的主要驱动力。城镇化扩张引起生活污水及富铵工业废水的泄漏入渗是城乡结合部高铵地下水铵氮的重要来源。三角洲平原区中性至弱碱性富含有机质的还原环境是高铵地下水的主要成因。风化溶滤、阳离子交换吸附、海陆交互作用是珠江三角洲高铵地下水质演变的主要水文地球化学过程。  相似文献   
68.
论四川盆地三叠系地下水水文地质条件   总被引:3,自引:0,他引:3       下载免费PDF全文
四川盆地三叠系地下水可划分出碎屑岩孔隙裂隙和碳酸盐岩岩溶裂隙两大储集类型。按此处构造开启程度和埋深条件等的不同,下中三叠统地下水有沉积变质水和渗入淋滤水两种基本成因类型,水动力特征各异。沉积变质水处于深埋封闭条件,受地静压力驱动控制;渗入淋滤水分布于背斜露头区和浅部地区,受静水压力驱动控制。并由此控制了盆地三叠系盐类的保存条件。  相似文献   
69.
The study area in the northwest Sinai represents one of the most significant regions in the Egyptian basement intensely invaded by post-orogenic calc-alkaline dyke swarms. Two post-orogenic dyke swarms have been recognized in NW Sinai namely: (1) mafic dykes of basalt, basaltic andesite and andesite composition and (2) felsic dykes of dacite, rhyodacite and rhyolite composition. These basaltic to rhyolitic dykes intruded contemporaneously and shortly after the intrusion of the post-orogenic leucogranite. The mafic and felsic dykes are enriched in incompatible elements, especially in the large ion lithophile elements (e.g. K, Rb, Ba) and depleted in high field strength elements with negative P, Ti and Nb anomalies. Major and trace element geochemistry indicates that investigated mafic and felsic magma types are not related via fractional crystallization. The protoliths of the mafic and felsic dykes appear to have evolved from different parental magmas. The incompatible trace element patterns favour a derivation of the mafic dykes from melting of a garnet peridotite source followed by fractional crystallization of olivine, clinopyroxene amphibole and zircon. The felsic dykes, on the other hand, could be generated by melting of garnet-free source modified subsequently by fractional crystallization of plagioclase, apatite and titanomagnetite. This implies variable source characteristics at the end of the Pan-African in the NW Sinai.The mafic and felsic dykes can be related to an intracontinental setting and that this was accompanied by a chemical evolution of the subcontinental lithosphere. Magma generation and ascent in the area was favoured by extensional movements, which is already known from other areas in NE Africa.  相似文献   
70.
Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria (IRB hereafter) in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As (Ⅲ)] removal. The floc samples were collected from two drinking water plants using IRB (Jyoyo and Yamatokoriyama, Japan), and our pilot - scale test site where arsenic and iron removal using IRB is under way (Mukoh, Japan). The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As (Ⅲ) and As(Ⅴ) sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 (Hyogo, Japan). FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in +5 valence state when As (Ⅲ) (or As (Ⅴ)) was added in laboratory sorption test, Fe in +3 valence state, and Mn a mixture of+3 and +4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As (Ⅲ) associated with IRB or change in arsenic binding with sorption site were the probable mechanism.  相似文献   
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