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1.
采于墨西哥湾GC238海底天然气渗漏区浅表层的冷泉碳酸盐岩呈结核状产出,由方解石微晶和胶结物及少量的黄铁矿构成。胶结物由直径为0.1~0.5 m的方解石化的球体、卵形体、棒状体组成,充填于方解石晶体之间。冷泉碳酸盐岩结核下表面发育有由方解石化的球体、卵形体、棒状体组成的薄层,其中的一些球状集合体(约5 m)断面显示发育有核和外壳的层圈结构。黄铁矿呈草莓状,也具有相似的层圈结构。这种层状结构与活体古细菌被硫酸盐还原细菌包裹的层圈结构相似。样品中所保存的球体、卵形体、棒状体及其所组成的层圈结构可能是石化的甲烷氧化古细菌和硫酸盐还原细菌。  相似文献   
2.
1IntroductionThe tropical West Pacific warm pool(TWP-WP),which spans an area roughly between10°Nto10°S of the equator from Indonesia to the dateline,has the world’s warmest sea surface temperature ofbeing greater than29℃.With the increase of recog-niz…  相似文献   
3.
Based on the recent research results on dry and wet deposition of nutrient elements and sulphate,we estimate the atmospheric flux of nutrient elements and sulphate to the southern Yellow Sea and the East China Sea in each season.The results suggest that the concentrations of nutrient elements and sulphate in aerosol and precipitation show an apparent seasonal cycle with the maximum values in winter and the minimum values in summer.Depositions of nitrate and sulphate are dominated by wet deposition,while the deposition for phosphate is mainly dry deposition.Moreover,compared with the riverine inputs,the atmospheric deposition may be the main source of dissolved inorganic nutrients in the southern Yellow Sea and the East China Sea.  相似文献   
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5.
自生碳酸盐矿物的分布特点,是体现孔隙水地球化学特征的一个侧面。在布莱克海岭气体水合物赋存的沉积区域里(ODP994#、995#、997#)就利用这点来评价成岩作用。碳酸盐矿物的分布特点揭示了三个独特的成岩分带:(1)在上部20mbsf (bsf:below seafloor,海底以下深度)处的碳酸盐矿物主要是生物成因的,没有显示成岩作用的存在。这个区域的方解石FOC和8180值(PDB)反映了海相碳酸盐的特点,是与海水平衡的条件下沉淀形成的;(2)在20mbsf和100mbsf深度,方解石的FOC值明显呈现负数(低至-7.0‰),自生白云石较普遍可见(2—40wt%),δ^13C值在3.6‰~13.7‰之间;(3)在,100mbsf以下,白云石从含量丰富减低至微量分布,而分散状的菱铁矿成为主要出现的矿物。菱铁矿的δ^1C和δ^18O值分别在5.0‰~10.9‰、2.9‰~7.6‰之间变化。把溶解无机碳(DIC)的δ^1C剖面分布特点和孔隙水的浓集梯度趋势与自生碳酸盐矿物的δ^13C和δ^18O值对比,我们发现,自生碳酸盐矿物在一个独特的深度区域里形成,呈带状分布。在20mbsf深度及以下,无机碳的δ^13C DIC出现最小负值(≤-38‰)、方解石白云石出现δ^13C负值,这种现象的出现是伴随着孔隙水碱度的增加、硫酸盐的亏损和孔隙间Ca^ 2 、Mg^ 2 离子的减少一起发生的,这表明自生方解石和自生白云石的形成是在硫酸盐还原带的底部开始(21mbsf左右)而在100mbsf附近深处大量出现。菱铁矿的形成很显然是在120~450mbsf之间发生,这个区间在气体水合物赋存的沉积物区域内和上部(赋存区域200—450mbsf)。菱铁矿的δ^13C和δ^18O值从它们出现的薄层一直到沉积物底部都几乎一致。然而,现在孔隙水中的δ^13C DIC仅仅与120~450mbsf间的菱铁矿的δ^13C值相似。此外,从菱铁矿中计算出来的与之平衡的δ^18O值与120~450mbsf区段处菱铁矿的δ^18O测量值很好地匹配起来。该区段以高碱度(40-120mm)、低Ca^ 2 、Mg^ 2 浓集度为特征,这符合菱铁矿的形成条件。  相似文献   
6.
本文提出了东海沉积物间隙水中溶解硅酸盐和硫酸盐的“扩散-平流-反应”模式。研究结果表明,由于间隙水受到硅酸盐溶解、吸附和沉淀不同体系的控制,因而间隙水中的硅酸盐具有三种不同形式的垂直分布,并从模式中得到了上述反应的反应常数,其中E柱硅溶解的一级动力学反应常数为0.00l 42a~(-1)。首次发现了东海沉积物间隙水中硅酸盐指数下降的垂直分布规律,并从数学模式上进行了处理。本文还研完了由于有机质还原sO_4~(2-)而产生的硫酸盐指数下降垂直分布,提出其模式,结果表明,SO_4~(2-)还原最大速率发生在沉积物-水界面附近,每年可达lmmo1/dm~3。  相似文献   
7.
The effect of Rayleigh distillation by outgassing of SO2 and H2S on the isotopic composition of sulfur remaining in silicate melts is quantitatively modelled.A threshold mole fraction of sulfur in sulfide component of the melts is reckoned to be of critical importance in shifting the δ^34S of the melts mith respect to the original magmas.The partial equilibrium fractionation in a magmatic system is evaluated by assuming that a non-equilibrium flux of sulfur occurs between magmatic volatiles and the melts,while an equilibrium fractionation is approached between sulfate and sulfide within the melts.The results show that under high fo2 conditions,the sulfate/sulfide ratio in a melt entds to increase,and the δ^34S value of sulfur in a solidified rock might then be shifted in the positive direction.This may either be due to Rayleigh outgassing in case the mole fraction of sulfide is less than the threshold,or due to a unidirectional increase in δ^34S value of the sulfate with decreaing temperature,Conversely,at low fo2,the sulfate/sulfide ratio tends to decrease and the δ^34S value of total sulfur could be driven in the negative direction,either because of the Rayleigh outgassing in case the mole fraction of sulfide is greater than the threshold,or because of a unidirectional decrease inδ^34S value of the sulfide.To establish isotopic equilibrium between sulfate and sulfide,the HM,QFM or WM buffers in the magmatic system are suggested to provide the redox couple that could simultaneously reduce the sulfate and oxidize the sulfide.CaO present in the silicatte Melts is also called upon to participate in the chemical equilibrium between sulfate and sulfide,Consequently,the δ^34S value of an igneous rock could considerably deviate from that of its original magma due to the influence of oxygen fugacity and temperature at the time of magma solidification.  相似文献   
8.
The purpose of the thesis is to analyze the temporal and dimensional distribution of sulfate-reducing bacteria (SRB) groups and quantity in Lake Erhai. In April and September 2005, two sediment cores were collected from Lake Erhai. SRB groups were analyzed by PCR with six-groups primers designed according to the specific 16SrDNA sequence. FISH (fluorescence in-situ hybridization) was established with the oligonucleotide probe (SRB385) and utilized to analyze SRB quantity in the sediments. The results showed that in the sediments of Lake Erhai four SRB groups were detected except Desulfobacterium and Desulfobacter, meanwhile Desulfovibrio-Desulfomicrobium were detected only in autumn; different SRB groups had different temporal and dimensional distribution, and each group in autumn is distributed more widely than in spring; FISH used to count SRB in the sediments of fresh lake was set up successfully; the analysis of correlation between the sediment's depth and SRB quantity had statistical meaning (P〈0.05) . The result showed that SRB quantity showed a decreasing trend with increasing depth. Through the analysis of randomized block designed analysis of variance, the difference in SRB quantity between spring and autumn also had statistical meaning (P〈0.001), which revealed SRB quantity in autumn was larger than in spring; the result of FISH showed that there were some SRB in the deeper sediments in which no above-mentioned six SRB groups were detected by PCR. SRB groups in the sediments of Lake Erhai were rich, and the quantities of SRB groups in autumn were larger than in spring; possibly there were uncultivable SRB groups in the sediments of Lake Erhai.  相似文献   
9.
Uranium processing and mining activities that generate many contaminants, such as high concentrations of U (VI), sulfate and heavy metals (Zn, Cu, Ni, etc), may pose a serious threat to the groundwater resources. In recent years, considerable research has been conducted respectively on two kinds of permeable reactive barriers (PRB), including zerovalent iron (ZVI) and sulfate reducing bacteria (SRB), for in-situ removal of these pollutants from groundwater. However, little investigation has been carried out on the potential benefits of bioaugmenting ZVI barriers to enhance the elimination of the pollutants by combining ZVI with SRB systems. The main goal of this study was to conduct batch and column experiments to determine whether the combination of SRB and ZVI can function synergistically and accelerate the rate of pollutant removal. The results of anaerobic batch experiments demonstrated that although the integrated ZVI/PRB system itself has no ability to reduce and remove sulfate directly, SRB can utilize hydrogen gas produced during the slow process of ZVI corrosion as an electron donor to raise biomass yields significantly and accelerate reductive sulfate removal. In particular, ferrous cations produced as the byproduct of ZVI corrosion process reacted with hydrogen sulfide from sulfate reduction and formed iron-bearing sulfide precipitates, which can stimulate the growth of SRB and promote sulfate removal activity by eliminating the biotoxicity of hydrogen sulfide. It was also shown that secondary mineral products (pyrite/ferrous sulfide) formed as a consequence of microbial sulfate reduction and ZVI corrosion process can enhance the microbial precipitation of soluble U (VI) as insoluble uraninite(uranium dioxide).  相似文献   
10.
Sulfates are a main constituent of aerosols, which sulfate aerosols, it is necessary to determine what can cause various environmental problems sulfate ions are contained in these aerosols In the evaluation of the influence of In this study, sulfur K-edge XANES was used to determine sulfate species present in size-fractionated aerosol particles based on the post-edge structure after the main absorption peak in the XANES region. Aerosol samples were collected as part of the Japan-China joint project, "Asian Dust Experiment on Climate Impact" using a low-volume Andersen-type air sampler. XANES was measured at Beamline BL-9A at Photon Factory, Japan. A comparison of the XANES spectra of reference sulfate materials and aerosol samples collected in Tsukuba in Japan clearly showed that (NH4)2SO4 was the main sulfur species in particles with a smaller diameter and gypsum was the main sulfur species in particles with a larger diameter. A simulation of the XANES spectra by reference materials allows us to obtain the quantitative mixing ratios of the different sulfate species present in the aerosol samples. The presence of minor sulfur species other than (NH4)2SO4 and gypsum at the surface of mineral aerosols is suggested in our simulations and by a surface-sensitive conversion electron/He-ion yield XANES. In the absence of a contribution from a large dust event, the mole concentration of gypsum in the mineral aerosol fraction determined by XANES is similar to that of Ca which is determined independently using ion chromatography. This shows that the Ca and sulfate in the mineral aerosols are present only as gypsum. Considering that calcite is the main Ca mineral in the original material arising from an arid and semi-arid area in China, it is strongly suggested that gypsum is formed in aerosol during its long-range transportation by a reaction between calcite and sulfate ions.  相似文献   
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