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161.
本文通过环境背景值、风化壳地球化学、对流层(大气气溶胶)地球化学和人为地球化学异常,初步探讨了南极长城站地区的现代环境地球化学特征。分析表明:环境要素固有的地球化学性质、区域环境条件和自然环境演变之间具有深刻的内在联系。  相似文献   
162.
侯可军  李延河  万德芳 《矿床地质》2006,25(Z2):167-170
文章分析了辽宁太古代红透山铜矿中硫化物的多硫同位素组成和石英的硅氧同位素组成。δ34S在-0.7‰~+3.1‰,极差为3.8‰,平均值为0.21‰,与深部幔源硫相似。δ33S≈0.52δ34S,即δ33S=0(δ33S =δ33S-1000[(1+ δ34S/1000)0.515-1],不具有硫同位素非质量分馏效应,表明该矿床中的硫没有经历大气循环过程。矿石中石英的δ30Si分布在-0.8‰~+0.4‰之间,δ18O分布在+8.5‰~+9.5‰之间,与海底黑烟囱及热水喷气成因硅质岩的硅氧同位素组成相似。提出红透山铜矿为海底热液喷气沉积变质成因。  相似文献   
163.
密坑山锡矿田位于江西省会昌县西南约40km处。该区为一晚中生代破火山,火山岩为上侏罗统鸡笼嶂组流纹质凝灰熔岩及火山碎屑岩,火山口周围环状及放射状断裂发育,火山口中心为浅成相的密坑山似斑状钾长花岗岩中央岩株侵入体所充填。上世纪80年代以来,在该岩体与流纹质凝灰熔岩的内外接触带相继发现了岩背、淘锡坝、苦竹岽、矿背、上湾等一批大、中型锡多金属矿床或矿点,表明这一岩体对成矿具有重要的制约作用。  相似文献   
164.
2005年12月23日~24日,中国地质调查局分析质量检查组对江苏省地质调查研究院测试所承担的“江苏国土生态地球化学调查”多元素分析测试工作进行了最终成果评审和评级验收。检查组听取了情况汇报,了解了数据的使用情况,随后逐一审阅了54项分析指标的地球化学图,同时对外部标准控制样的各项质量参数进行了统计分析,并查阅了分析测试的原始记录。检查组认为,“江苏国土生态地球化学调查”项目土壤样品多元素分析工作的各项指标均达到或优于规范要求,地球化学图图面效果好,元素空间分布规律与地质背景特征和生态环境特征相吻合,分析数据准确、可…  相似文献   
165.
Element geochemistry of lake sediments has been widely used to detect climate change because element composition and ratios can reflect the weathering degree in the source area. Given the dement composition of lake sediments from Gulug Co Lake, Hoh Xil, Qing- hai-Xizang Plateau, chemical index of alteration (CIA), index of composition variability (ICV) and other element ratios have been used to establish the weathering sequence of this area since 1820 AD. The weathering is so weak that the element composition change is more sensitive to climate change and autochthonous processes. From 1820 to 1984 AD, there were two drier periods with a wetter interval from 1870 to 1945 AD. After 1984 the weather showed a tendency of becoming wet.  相似文献   
166.
Adsorption of arsenate on hydrous iron oxide is an important process controlling geochemical cycling of arsenic in environment as well as the fate of arsenic-bearing mining wastes. The widely accepted view on the mechanism of adsorption is that arsenate is adsorbed via bidentate binuclear inner-sphere complexation. In this study, we characterized the arsenate-hydrous iron oxide sorption solids synthesized at pH=3-8 using Fourier transformed infrared spectroscopy (FTIR) and X-ray diffraction (XRD). It has been determined that poorly crystalline ferric arsenate developed on the surface of iron oxide when arsenate was sorbed at acidic pH, while at alkaline pH the adsorption of arsenate was via bidentate complexation.  相似文献   
167.
Metals, including heavy metals and metalloids, are a common group of environmental contaminants. Their sources in the environment are geogenic or anthropogenic. The growing trend in global industrialization ensures that more metals could be dispersed even in pristine ecosystems. To fuel industrialization, more metal ore mines have to be discovered and explored. These explorations often result in landscape disturbance, soil degradation and environmental contamination by unwanted mining constituents. Mine tailings brought up to the ground surface often serve as the main source of contaminants when these pyrite-rich materials oxidize. The oxidation of mine tailings results in proton generation, coupled with the dissolution of metals and other cations Unwanted anionic constituents are also produced. The so-called "acid mine drainage" may affect the productivity of farmlands and stability of receiving streams and other bodies of water-acidifying the waters and enriching the ecosystem with metals, i.e., high total dissolved solids. The acidified overburden materials become inhospitable to plant and microbial life as they are typically low in organic matter content and infertile. This exposes the landscape to runoff and erosion.  相似文献   
168.
High concentrations of arsenic and humic substances in groundwater from the southwestern coastal plain of Taiwan were well known for their probable relationships with black-foot disease. In order to realize the relationships between the concentrations of humic substances and arsenic in this area, 24 well water samples were analyzed. After filtered through 0.45 μm glass fiber membrane in the field, samples were kept in the dark at 4℃ and then separated into six fractions with varying range of molecular weight (〈0.5, 0.5-1, 1-5, 5-10, 10-50 and 〉50 k Da) by ultrafiltration apparatus (Molecular/Por Stirred Cell system) in the lab. Concentrations of humic substances were measured by fluorescence spectrometer (HITACHI F-2000, ex=370, em=445) and arsenic by FIAS-AA (Perkin Elmer AAnalyst 100, FIAS-400). On average, only 6.2% of the total arsenic in water existed in the fraction of 〉0.5 k Da. and the others were complexed with humic substances (including humic acid and fulvic acid). The results demonstrated a distinct positive correlation between the concentrations of humic substances and arsenic.  相似文献   
169.
Background: Radiographic signs of Pneumoconiosis found in farming Ladakhi despite absences of mines and industries were believed to be due to exposure to frequent dust storms and domestic fire pollutions. Seasonal Koilonychia (spoon nail) occurring predominantly in farming women in absences of iron deficiency anaemia was thought to arise from exposure to water made alkaline by weathering of hornblende minerals. The relation of these health conditions to environmental geohydrochemistry is postulated as the source of irrigation water in the affected population originates from glaciers in trans-Himalaya range of sedimentary geology and steep landscape favouring flushing of silica/silicate containing silts. Methods and results: Survey in two central Ladakh villages revealed radiographic evidence of silicosis in all middle aged women and half in middle aged men. In a large-scale study of 3105 subjects aged over 30 years from three villages; 101 (22.5%) of the 449 radiographed showed signs of pneumoconiosis (ILO 1980 criteria) including eggshell calcification of hilar gland and progressive massive fibrosis. Indoor dust analyzed using Philips 400T electron microscope with energy dispersive analysis system attached showed SiO2 levels upto 53.27% with particle size of 0.5 to 5.0 microns and the concentration during cooking period in the worst affected area was 7.495 mg/m^3. Microscopy and histopathology from the subject was characteristic of pneumoconiosis. Analysis of the inorganic dust in the lung showed 40.2% muscovite, 37.3% quartz with the extracted dust wt 147.9 mg/gm of dry tissue. Prevalence of chronic cough with chronic phlegm and percentage of villagers with FEV1/FVC ratio of less than 65% rose with age. Of 70 subjects studied 19 women and 2 men had Koilonychia with incidence being highest in summer. Absence of seasonal Koilonychia in villages fed by water derived from northern mountain range glaciers with mainly igneous geology supports our hypothesis.  相似文献   
170.
Mt. Amiata (Southern Tuscany, Central Italy) is an extinct Quaternary volcano located in an area still marked by high heat-flow that is caused by deep seated (6-10 km) hot masses related to Pliocene magmatic activity. The anomalous geothermal gradient gives rise, within the Mesozoic limestone formation (Tuscan series), to geothermal systems that fed the Ca-SO4 thermal springs characterizing this area. Besides of thermal fluids, several cold, dry CO2-rich gas emissions seep out on the NE flank of the volcano. These gas vents mostly consist of large sub-circular craters at variable depth and diameter (5-15 m and 10-50 m, respectively), and represent a serious hazard for the local population, as testified by the several asphyxia casualties that have been repeatedly occurred within these morphological depressions. In this work, the chemical and isotopic compositions of the Mt. Amiata "CO2-rich gas vents" and the estimation of both the CO2 flux from the soil and the CO2 distribution in air of their surroundings, has been carried out in order to: (1) assess the origin of gases, (2) recognize the mechanism of formation for these gas emissions and their relationship with local tectonics, and (3) to evaluate the CO2 hazard in the high flux emanations. The chemical composition of the gases is largely dominated by CO2 (up to 98 % by vol) and shows relatively high concentrations of N2, CH4 and H2S (up to 1.1%, 0.9% and 3.9 % by vol, respectively). These features, coupled with the carbon and nitrogen isotopic signatures, suggest that the origin of the main gas compounds may be related to the contribution of deep (i.e., thermometamorphic processes on carbonate formations for CO2) and shallow (i.e. thermal decomposition of organic material for CH4, N2 and H2S) sources.  相似文献   
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