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51.
化学注浆治理巨厚表土层立井井壁漏水   总被引:1,自引:0,他引:1  
煤矿立井由于各种原因经常发生井壁渗漏水,严重影响正常的煤矿安全生产。邱集煤矿副立井表土层厚320m,为巨厚表土层,发生渗水后,采用改性脲醛树脂浆材成功进行了破壁注浆处理,将井筒的涌水量由10m3/h降至0.3m3/h左右。同时,注浆时浆液形成的帷幕能达到加固地层,减少地层压缩沉降量,排除生产安全隐患,保护井桶的作用。  相似文献   
52.
GDX-502树脂富集高效液相色谱法测定地表水中酚类化合物   总被引:2,自引:2,他引:2  
何淼  饶竹  苏劲  黄毅 《岩矿测试》2007,26(2):101-104
采用自制GDX-502固相萃取小柱萃取水中苯酚、对硝基酚、间甲酚、2,4-二氯酚、2,4,6-三氯酚、五氯酚等6种酚类化合物,以乙腈作为洗脱剂,选择280nm和290nm双波长紫外高效液相色谱进行检测。结果表明,方法检出限为0.01-0.05mg/L,IL水的平均加标回收率为82.5%-95.0%,精密度(RSD,n=7)为3.6%-9.2%。方法用于实际地表水中痕量酚类化合物的检测,操作简单,有机溶剂用量少,分析效率高;萃取小柱可多次重复使用,分析成本低。  相似文献   
53.
新疆包古图斑岩铜矿伴生元素金和银赋存状态初步研究   总被引:13,自引:0,他引:13  
新疆西准噶尔包古图斑岩铜矿床Au平均含量0.25g/t,Ag为2.56g/t,Cu为0.30%,属于富金斑岩铜矿。伴生金和银矿化作用有两期:早期为斑岩矿化,形成了Cu-Mo-Au矿化组合,是主矿化期;后期叠加了Cu-Au-Ag-Te-Bi矿化,规模不大,出露于矿床的局部部位,但对矿石起到了加富作用。通过对钻孔薄片和光薄片的镜下观察及电子探针成分分析,认为早期矿化中Au和Ag主要呈固溶体形式存在于硫化物中,分布比较均匀,基本上不出现独立矿物,Au含量明显高于Ag;晚期矿化形成了复杂的Cu-Au-Ag-Te-Bi矿物,矿石呈浸染状和脉状叠加在早期矿化之上,以银矿物为主,与多种碲铋类矿物共生,主要银矿物有碲银矿、铋-碲银矿(?)、银-辉碲铋矿(?)、银-硫铋铜矿、银金矿等。晚期矿化规模不大,但对于提高矿床的经济价值具有重要意义。  相似文献   
54.
Abstract: The Bulawan deposit is located in the porphyry copper belt of southwest Negros island, Philippines. Propylitic, K–feldspar, sericitic, and carbonate alteration types can be distinguished in the deposit. Propylite alteration occurs mainly in Cretaceous-Eocene andesitic lavas and agglomerates while K–feldspar, sericite and carbonate alteration types occur mostly in the Middle Miocene dacite porphyry breccia pipes and stocks which were intruded into the andesites. K-feldspar zones occur in the inner parts of the sericitized zone. Sericite alteration overprinted the propylitized and K-feldspar alteration zones, at lower temperature than epidote and chlorite in the propylitized zone. Carbonate alteration is associated with the mineralization in the center of the breccia pipes and along faults. Mineralization consists of gold-silver telluride ores that are hosted by the carbonate– and sericite-altered dacite porphyry breccia pipes. The Bulawan ores occur mainly as disseminations, but unlike many epithermal gold deposits, lack classical epithermal colloform and crustiform quartz veins. The ore minerals are sphalerite, galena, chalcopyrite, pyrite and tetrahedite-tennantite with minor amounts of electrum, calaverite, petzite, sylvanite, hessite, tellurobismuthite, coloradoite, altaite, and rucklidgeite. Electrum and telluride minerals are associated mostly with calcite and dolomite-ankerite minerals. Fluid inclusions in quartz and calcite in clasts of propylitized andesite in the breccia pipes homogenize from about 300° to 400°C while fluid inclusions in quartz, calcite and sphalerite within the dacite porphyry breccia pipes homogenize between 300° to 310°C. The ores were formed around 300°C from hydrothermal solutions with salinity of about 6. 6 wt % NaCl equivalent. The presence of sylvanite and calaverite as intergrowths with each other, and the Ag content of calaverite are consistent with the above temperature estimate. Based on paragenesis, the Bulawan deposit formed in a pyrite-stable environment, with pH between 3. 4 and 5. 5, fO2 between 10-32 to 10-30 atm, fS2 between 10-9.8 to 10-7.8 atm, fTe2 between 10-8.9 to 10-6.5 atm, and total sulfur content about 10-2.8 molal. The dominant reduced sulfur species in the ore solutions may have been H2S(aq), and the likely aqueous tellurium species were H2Te(aq) and H2TeO3(aq). The ore minerals in the Bulawan deposit were probably formed by mixing of slightly saline and low salinity fluids.  相似文献   
55.
金、铜、铅、锌(银)矿是辽宁地区的优势矿种,过去和现在都曾从多个不同角度或多个方面予以研究论述,但从成矿系列理论研究则是作者(1994)在Ⅱ轮区划工作中所做的一种新的尝试。根据程裕淇先生的成矿系列理论,辽宁地区早前寒武纪变质岩系中的金、铜、铅、锌(银)矿床属变质成矿系列组合,可进一步划分为三个成矿系列,六个成矿亚系列,九个矿床(种)类型和十二个矿床式。成矿系列特征表明成矿物质与原岩的含矿性关系非常密切,成矿物质或元素具有随原岩建造时空演化而演化的特点,成矿具有鲜明的专属性和层控性,是典型或比较典型的层控变质矿床。金矿床的形成和分布均与韧性剪切带及其糜棱岩有关,表明辽宁前寒武纪金矿床的形成不仅与变质作用有关,而且韧性剪切作用也是极其重要的成矿条件;铜、锌(银)和铅、锌(银)矿床以块状硫化物型为主,其成矿多与火山作用关系十分密切,变质作用过程中,发生重就位或再富集,或热液交代富集成矿。由太古宙至早元古代不同成矿系列或成矿亚系列中的矿床具有自下而上有序的空间分布规律。  相似文献   
56.
黄斑篮子鱼去毒相关基因的克隆与肝脏组成型表达分析   总被引:1,自引:0,他引:1  
从基因水平探讨海洋鱼类对海洋藻毒素的去毒分子机理。采用RT-PCR法成功克隆了黄斑篮子鱼Siganus oramin肝脏I时相代谢酶细胞色素P450 1A(CYP1A)、II时相代谢酶alpha型谷胱甘肽S-转移酶(GSTA)和rho型谷胱甘肽S-转移酶(GSTR)、热休克蛋白70 (HSP70)、alpha 1型钠钾ATP酶(ATP1A1)及β-肌动蛋白(beta-actin, ACT)基因cDNA核心序列,序列分别长879 bp、582 bp、588 bp、660 bp、749 bp和554 bp。序列同源性分析发现,属鲈形目的黄斑篮子鱼CYP1A、GSTA和GSTR与同属鲈形目的牙鲆Paralichthys olivaceus、欧洲鲽Pleuronectes platessa、真鲷Pagrus major、鲤形目的斑马鱼Brachydanio rerio 相应氨基酸序列同源性较高,CYP1A和GSTA与非洲爪蟾(两栖类)、鸡(鸟类)、小鼠、大鼠和人(哺乳类)相应氨基酸序列同源性低,这可能与鱼类I、II时相去毒酶基因承担水环境毒素去毒代谢的特殊功能有关;而HSP70、ATP1A和β-肌动蛋白在鱼类、两栖类、鸟类、哺乳类中均有较高的同源性,这可能与这些基因在机体中承担的最基本的生命功能相关。应用半定量RT-PCR的方法,以β-肌动蛋白作为外参照,在指数期增长范围内分别得到了CYP1A、GSTA、GSTR、HSP70和ATP1A1 mRNA与β-肌动蛋白mRNA (%)的比值,确定黄斑篮子鱼肝脏去毒相关基因的组成型表达水平。其中,黄斑篮子鱼肝脏CYP1A、GSTA和GSTR基因组成型表达相对较高,HSP70和ATP1A1基因组成型表达相对较低,这可能与不同基因在黄斑篮子鱼海洋藻毒素去毒分子机理中承担的作用相关,为海洋藻毒素在海洋鱼类中的积聚及代谢去毒分子机制的研究提供了相关数据。  相似文献   
57.
Dissolved and particulate concentrations of silver in Tokyo Bay estuarine waters and Japanese rivers were determined in this study. The dissolved silver concentrations in the surface water of Tokyo Bay range from 5.9 to 15.1 pmol kg−1, which is comparable to those in the surface water of the Japan Sea, but two or three times higher than those in the surface water of the open ocean. However, elevated concentrations of dissolved silver are not found in Tokyo Bay compared with those in other highly urbanized estuaries, such as San Francisco Bay (20∼243 pmol kg−1). In the Tokyo Bay estuary, silver typically exhibits non-conservative mixing behavior, which is a common feature in the other estuaries reported previously. Dissolved silver concentrations decrease with salinity from the rivers to the mouth of Tokyo Bay. Silver is efficiently scavenged by suspended particulates, as evidenced by the high conditional distribution coefficients for silver throughout the estuary (log Kd > 5.0 ± 0.6). The silver fluxes into Tokyo Bay via inflowing rivers and atmospheric deposition were estimated as 83 kg y−1 and 15 kg y−1, respectively. A simple budget calculation shows that the silver supplied from rivers and atmosphere must be rapidly scavenged within the Tokyo Bay estuary.  相似文献   
58.
The Lanping basin is a significant Pb–Zn–Cu–Ag mineralization belt of the Sanjiang Tethyan metallogenic province in China. Over 100 thrust-controlled, sediment-hosted, Himalayan base metal deposits have been discovered in this basin, including the largest sandstone-hosted Pb–Zn deposit in the world (Jinding), and several Cu ± Ag ± Co deposits (Baiyangping, Baiyangchang and Jinman). These deposits, with total reserves of over 16.0 Mt Pb + Zn, 0.6 Mt Cu, and 7000 t Ag, are mainly hosted in Meso-Cenozoic mottled clastic rocks, and strictly controlled by two Cenozoic thrust systems developed in the western and eastern segments of the Lanping basin.To define the metallogenic history of the study area, we dated nine calcite samples associated with copper sulfides from the Jinman Cu deposit by the Sm–Nd method and five molybdenite samples from the Liancheng Cu–Mo deposit by the Re–Os method. The calcite Sm–Nd age for the Jinman deposit (58 ± 5 Ma) and the molybdenite Re–Os age for the Liancheng deposit (48 ± 2 Ma), together with previously published chronological data, demonstrate (1) the Cu–Ag mineralization in the western Lanping basin mainly occurred in three episodes (i.e., ∼56–54, 51–48, and 31–29 Ma), corresponding to the main- and late-collisional stages of the Indo–Asian orogeny; and (2) the Pb–Zn–Ag (±Cu) mineralization in the eastern Lanping basin lacked precise and direct dating, however, the apatite fission track ages of several representative deposits (21 ± 4 Ma to 32 ± 5 Ma) may offer some constraints on the mineralization age.  相似文献   
59.
A new method for the direct determination of reduced and oxidized Mo species (Mo (V) and Mo (VI)) in seawater was developed and used for the first time. The method includes the complexation of Mo (V) with tartrate, solid phase extraction of the Mo (V)–tartrate complex by a XAD 7HP resin, followed by elution with acidic acetone. In this study, the eluted Mo (V) was quantified by graphite furnace atomic absorption spectrometry. The detection limit of this protocol was on the order of 0.2 nM. The analytical precision was 10% of ~ 10 nM. This method was successfully applied to the determination of Mo (V) and Mo (VI) in surface and bottom waters at the head of Peconic River Estuary. Total Mo (Mo (V) + Mo (VI)) ranged from 100–120 nM in most bottom saline waters, and 2.5–15 nM for surface fresher waters. Concentrations of Mo (V) in these environments ranged from 0 nM to ~ 15 nM, accounting for 0%–15% of the total dissolved Mo pool. The time series experiments showed that the Mo speciation changed within 1 h after the water collection, and therefore it is strongly suggested that speciation analysis be carried out within the first 15 min. However, since these are the first Mo speciation data in concentration ranges typical of normal marine and coastal waters, additional research may be required to optimize the methodology and further explore Mo cycling mechanisms.  相似文献   
60.
The concentrations of cadmium, phosphorus, and aluminum in size-fractionated phytoplankton, zooplankton, and sinking particles are determined using ICPMS to evaluate the roles of biotic and abiotic particles on the cycling and ratios of Cd and P in the water column. Plankton were collected with a filtration apparatus equipped with 10-, 60-, and 150-μm aperture plankton nets on two occasions (2002 and 2006), and sinking particles were sampled by moored sediment traps deployed at depths of 120, 600, and 3500 m from 2004 to 2005. In contrast to what our previous study revealed, i.e., that most of the other bioactive trace metals in plankton were strongly correlated with abiotic Al and adsorbed on phytoplankton [Ho, T.Y., Wen, L.S., You, C.F., Lee, D.C., 2007. The trace metal composition of size-fractionated plankton in the South China Sea: biotic versus abiotic sources. Limnol Oceanogr 52, 1776–88.], Cd/P ratios, ranging from 0.12 to 0.34 mmol/mol P, did not vary with Al and exhibited fairly consistent values among different sizes of plankton, showing that Cd was mostly incorporated on an intracellular basis. In terms of the sinking particles, fluxes in Cd and P as well as in Cd/P ratios were strongly influenced by both biotic and abiotic particles. Overall, the Cd/P ratios in the sinking particles ranged from 0.03 to 1.2 mmol/mol, with the highest value observed in traps at 120 m during the productive season. The lowest value was observed in deep water during high flux periods for lithogenic particles. At surface depth, flux and Cd/P ratios were elevated during the most productive season in the region. The elevated ratios in the traps at 120 m were most likely related to preferential uptake of Cd for the dominant species (coccolithophores) during the productive period. Relatively, Cd/P ratios sharply decreased with increasing Al flux in deep water and ratios were much lower than the expected Cd/P ratios obtained from the relative portion of lithogenic and biogenic particles, indicating that the adsorption of soluble P into lithogenic particles was significant in the deep water during high lithogenic particle flux periods. Using averaged annual fluxes and standing stock in the water column, the residence time of biogenic Cd and P are 0.10 and 0.20, 250 and 100, and 9100 and 5000 years respectively in the top 120 m, 600 m, and water column as a whole, also showing preferential removal for Cd in the euphotic zone but relatively higher removal rates for P in the deep water. Our study suggests that the shift in microalgal community structure along with input of lithogenic minerals are both potentially important factors in influencing Cd/P ratios in oceanic water on a geological time scale.  相似文献   
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