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1.
A 43 cm long E271 sediment core collected near the East Pacific Rise(EPR) at 13°N were studied to investigate the origin of smectite for understanding better the geochemical behavior of hydrothermal material after deposition.E271 sediments are typical metalliferous sediments. After removal of organic matter, carbonate, biogenic opal,and Fe-Mn oxide by a series of chemical procedures, clay minerals(2 μm) were investigated by X-ray diffraction,chemical analysis and Si isotope analysis. Due to the influence of seafloor hydrothermal activity and close to continent, the sources of clay minerals are complex. Illite, chlorite and kaolinite are suggested to be transported from either North or Central America by rivers or winds, but smectite is authigenic. It is enriched in iron, and its contents are highest in clay minerals. Data show that smectite is most likely formed by the reaction of hydrothermal Fe-oxyhydroxide with silica and seawater in metalliferous sediments. The Si that participates in this reaction may be derived from siliceous microfossils(diatoms or radiolarians), hydrothermal fluids, or detrital mineral phases. And their δ30 Si values are higher than those of authigenic smectites, which implies that a Si isotope fractionation occurs during the formation because of the selective absorption of light Si isotopes onto Feoxyhydroxides. Sm/Fe mass ratios(a proxy for overall REE/Fe ratio) in E271 clay minerals are lower than those in metalliferous sediments, as well as distal hydrothermal plume particles and terrigenous clay minerals. This result suggests that some REE are lost during the smectite formation, perhaps because their large ionic radii of REE scavenged by Fe-oxyhydroxides preclude substitution in either tetrahedral or octahedral lattice sites of this mineral structure, which decreases the value of metalliferous sediments as a potential resource for REE.  相似文献   
2.
The authors analyzed the data collected in the Ecological Station Jiaozhou Bay from May 1991 to November 1994, including 12 seasonal investigations, to determine the characteristics, dynamic cycles and variation trends of the silicate in the bay. The results indicated that the rivers around Jiaozhou Bay provided abundant supply of silicate to the bay. The silicate concentration there depended on river flow variation. The horizontal variation of silicate concentration on the transect showed that the silicate concentration decreased with distance from shorelines. The vertical variation of it showed that silicate sank and deposited on the sea bottom by phytoplankton uptake and death, and zooplankton excretion. In this way, silicon would endlessly be transferred from terrestrial sources to the sea bottom. The silicon took up by phytoplankton and by other biogeochemical processes led to insufficient silicon supply for phytoplankton growth. In this paper, a 2D dynamic model of river flow versus silicate concentration was established by which silicate concentrations of 0.028–0.062 μmol/L in seawater was yielded by inputting certain seasonal unit river flows (m3/s), or in other words, the silicate supply rate; and when the unit river flow was set to zero, meaning no river input, the silicate concentrations were between 0.05–0.69 μmol/L in the bay. In terms of the silicate supply rate, Jiaozhou Bay was divided into three parts. The division shows a given river flow could generate several different silicon levels in corresponding regions, so as to the silicon-limitation levels to the phytoplankton in these regions. Another dynamic model of river flow versus primary production was set up by which the phytoplankton primary production of 5.21–15.55 (mgC/m2·d)/(m3/s) were obtained in our case at unit river flow values via silicate concentration or primary production conversion rate. Similarly, the values of primary production of 121.98–195.33 (mgC/m2·d) were achieved at zero unit river flow condition. A primary production conversion rate reflects the sensitivity to silicon depletion so as to different phytoplankton primary production and silicon requirements by different phytoplankton assemblages in different marine areas. In addition, the authors differentiated two equations (Eqs. 1 and 2) in the models to obtain the river flow variation that determines the silicate concentration variation, and in turn, the variation of primary production. These results proved further that nutrient silicon is a limiting factor for phytoplankton growth. This study was funded by NSFC (No. 40036010), and the Director's Fund of the Beihai Sea Monitoring Center, the State Oceanic Administration.  相似文献   
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素土桩挤密地基由桩间挤密土和回填素土夯实的桩体组成,它是一种人工“复合地基”。其作用是通过素土桩挤密法提高地基土的密实度,从而对湿陷性黄土达到消除浅部或深部的部分或全部湿陷性的作用,并改善地基承载能力,减少地基变形。本文通过现场单桩、群桩单元体轻便触探、小环刀深层取样、开剖取样等方法对场地地基土挤密前、后干重度和压实系数进行了对比分析,判定用素土桩挤密法处理陇东湿陷性黄土地基的可行性。  相似文献   
5.
在查明搭格架铯矿床产出的地质背景、成矿阶段及其年龄、地球化学与同位素组成的基础上,本文较为系统地研究了硅华的矿物学与组构特征,加深了对硅华形成演化过程的认识.研究表明成矿早期,矿石中存在大量的石英,晚期全为蛋白石.粒状蛋白石自早到晚均有出现,胶状蛋白石主要出现于晚期.早期矿石出现脱水造成的菜花状、粗粒块状与粗大孔隙状构造及溶蚀结构.晚期出现细粒块状与细小孔隙状构造.在第3阶段存在硅藻Denticula属,体现出低温阶段的特征.由早到晚,矿石的SiO2呈降低趋势,而(Na2O Al2O3 K2O CaO)与Cs2O呈升高趋势,是随着矿石中SiO2有序度的降低而其它成分被保留在晶格中所致.  相似文献   
6.
王辉  冯士笮 《海洋与湖沼》1995,26(2):161-168
基于拉格朗日余流及其输运过程的一种三维空间弱非线性理论,进一步假定Si在河口的无因次化学转移项量级为k^2,给出了Si的长期输运方程。对于一种二维模型河口,数值求解了零阶天文潮,欧拉余流、斯托克斯漂移、拉格朗日余流和盐度的分布;分别计算了平均逼留时间为13,30,60,180d等所对应的Si浓度分布;给出了Si-s相关图,讨论了河口中Si的保守性问题。  相似文献   
7.
长江生源要素的输出通量   总被引:6,自引:2,他引:6  
长江是太平洋西岸最大的河流,它源源不断地向东海输送大量物质,是舟山渔场的重要化学物质基础,不仅对长江口海区以至整个东海有举足轻重的影响,对太平洋的影响也是不可忽视的。本文报道颗粒有机碳(POC)、溶  相似文献   
8.
对取自冲绳海槽北段的6个沉积岩心进行了CaCO3含量、粒度和铀系同位素分析,结合氧同位素数据和海槽其他钻孔的相应结果,探讨了冲绳海槽北部晚第四纪以来CaCO3含量的垂向与横向变化特征。结果表明,冲绳海槽北段沉积总体上表现为全新世CaCO3含量高、晚更新世CaCO3含量低的“大西洋型”碳酸盐演化特征,但冲绳海槽北段和中部的碳酸盐演化特征并不一致,海槽内西坡、槽底和东坡的不同部位其演化特征也存在较大差异。碳酸盐含量的变化与沉积物粒度特征密切相关,晚第四纪冲绳海槽碳酸盐演化的时空差异是多种因素相互作用的结果。  相似文献   
9.
本文就山东省海积型硅砂资源的开发应用现状及今后进一步的开发应用进行了探讨。  相似文献   
10.
南沙群岛海域沉积物间隙水营养盐(氮、磷、硅)的研究   总被引:14,自引:2,他引:14  
通过1997年11月和1999年7月2个航次对南沙群岛海域的现场调查,实测了南沙群岛深海盆沉积物的孔隙度?间隙水的营养盐含量,估算了沉积物海水界面营养盐的扩散通量?2个航次的沉积物间隙水的NO2-N,NO3-N ,NH4-N,PO4-P ,SiO3-Si含量,1997年冬季航次平均为4.68,43.84,115.68 ,6.85,425.71μmol·L-1,1999年夏季航次(H4SiO4除外)平均为2.72,36.86,31.40,10.10μmol·L-1;平均扩散通量,1997年冬季航次为0.03,-14.07,121.70,0.25,72.54μmol·m-2·d -1,1999年夏季航次(H4SiO4除外)为0.10,-11.74,40.47,-0.56μmol·m-2·d -1?NH 4和H4SiO4 是扩散量最大的2种组分,而HPO2-4 和NO-2的扩散量极小?  相似文献   
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