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61.
Road construction through sulfidic materials in Virginia has resulted in localized acid rock drainage (ARD) that threatens water quality, sedimentation, integrity of building materials, and vegetation management. Geologic formations associated with acid roadcuts were characterized by potential peroxide acidity (PPA), expressed as calcium carbonate equivalence (CCE), and total sulfur (total-S) in order to develop a statewide sulfide hazard rating map. The geologic formations were grouped into four categories based on potential acid-producing severity: i) Tabb formation (PPA<6 Mg CCE/1000 Mg; S<0.2%); ii) Ashe formation (PPA<18 Mg CCE/1000 Mg; S<2.0%); iii) Chesapeake Group, Lower Tertiary deposits, Millboro shale, Marcellus shale, and Needmore Formation (PPA<60 Mg CCE/1000 Mg; S<2.6%), and; iv) Chattanooga shale and Quantico slate (PPA<99 Mg CCE/1000 Mg; S<3.9%). Sulfide hazard analysis should be an essential step in the pre-design phase of highway construction and other earth-disturbing activities.  相似文献   
62.
SW Iberia is interpreted as an accretionary magmatic belt resulting from the collision between the South Portuguese Zone and the autochthonous Iberian terrane in Variscan times (350 to 330 Ma). In the South Portuguese Zone, pull-apart basins were filled with a thick sequence of siliciclastic sediments and bimodal volcanic rocks that host the giant massive sulphides of the Iberian Pyrite Belt. Massive sulphides precipitated in highly efficient geochemical traps where metal-rich but sulphur-depleted fluids of dominant basinal derivation mixed with sulphide-rich modified seawater. Massive sulphides formed either in porous/reactive volcanic rocks by sub-seafloor replacement, or in dark shale by replacement of mud or by exhalation within confined basins with high biogenic activity. Crustal thinning and magma intrusion were responsible for thermal maturation and dehydration of sedimentary rocks, while magmatic fluids probably had a minor influence on the observed geochemical signatures.The Ossa Morena Zone was a coeval calc-alkaline magmatic arc. It was the site for unusual mineralization, particularly magmatic Ni–(Cu) and hydrothermal Fe-oxide–Cu–Au ores (IOCG). Most magmatism and mineralization took place at local extensional zones along first-order strike-slip faults and thrusts. The source of magmas and IOCG and Ni–(Cu) deposits probably lay in a large mafic–ultramafic layered complex intruded along a detachment at the boundary between the upper and lower crust. Here, juvenile melts extensively interacted with low-grade metamorphic rocks, inducing widespread anatexis, magma contamination and further exsolution of hydrothermal fluids. Hypersaline fluids (δ18Ofluid > 5.4‰ to 12‰) were focused upward into thrusts and faults, leading to early magnetite mineralization associated with a high-temperature (> 500 °C) albite–actinolite–salite alteration and subsequent copper–gold-bearing vein mineralization at somewhat lower temperatures. Assimilation of sediments by magmas led in turn to the formation of immiscible sulphide and silicate melts that accumulated in the footwall of the layered igneous complex. Further injection of both basic and sulphide-rich magmas into the upper crust led to the formation of Ni–(Cu)-rich breccia pipes.Younger (330 to 280 Ma?) peraluminous granitoids probably reflect the slow ascent of relatively dry and viscous magmas formed by contact anatexis. These granitoids have W–(Sn)- and Pb–Zn-related mineralization that also shows geochemical evidence of major mantle–crust interaction. Late epithermal Hg–(Cu–Sb) and Pb–Zn–(Ag) mineralization was driven by convective hydrothermal cells resulting from the high geothermal gradients that were set up in the zone by intrusion of the layered igneous complex. In all cases, most of the sulphur seems to have been derived from leaching of the host sedimentary rocks (δ34S = 7‰ to 20‰) with only limited mixing with sulphur of magmatic derivation.The metallogenic characteristics of the two terranes are quite different. In the Ossa Morena Zone, juvenile magmatism played a major role as the source of metals, and controlled the styles of mineralization. In the South Portuguese Zone, magmas only acted as heat sources but seem to have had no major influence as sources of metals and fluids, which are dominated by crustal signatures. Most of the magmatic and tectonic features related to the Variscan subduction and collision seem to be masked by those resulting from transpressional deformation and deep mafic intrusion, which led to the development of a metallogenic belt with little resemblance to other accretionary magmatic arcs.  相似文献   
63.
Volcanic rocks from Serra Branca, Iberian Pyrite Belt, Portugal, consist of calc-alkaline felsic and intermediate rocks. The latter are massive andesites, whereas the former include four dacitic to rhyolitic lithologies, distinguishable on spiderdiagrams and binary plots of immobile elements. Zircon thermometry indicates that two felsic suites may have formed from different magmas produced at distinct temperatures, with only limited fractionation within each suite. Alternatively, all the felsic rocks can be related through fractionation of a single magma if the lower zircon saturation temperature obtained for one suite merely results from Zr dilution, mostly reflecting silicification.

The relatively high magma temperatures at Serra Branca ease the classification of felsic rocks based on their HFSE contents and also indicate volcanogenic massive sulfide deposit favorability. This contrasts with other areas of the Belt that register lower magma temperatures and are subsequently barren. However, magma temperatures may have not been high enough to cause complete melting of refractory phases in which HFSE reside during crustal fusion of an amphibolite protolith, implying difficult discrimination of tectonic environments for the felsic rocks. The intermediate rocks were possibly formed by mixing between basaltic magmas and crustal material, compatible with volcanism in an attenuated continental lithosphere setting.  相似文献   

64.
峪耳崖金矿黄铁矿的标型特征研究   总被引:3,自引:0,他引:3  
吴丹  廖香俊 《矿产与地质》1998,12(3):183-187
峪耳崖金矿黄铁矿的形态、粒度、化学成分、热电系数、硫同位素特征表明:黄铁矿的金含量由早阶段至晚阶段随着自形程度降低、粒度变小而增高;峪耳崖金矿北矿带7中段以下仍有矿脉延伸;峪耳崖金矿的硫来源于深部。  相似文献   
65.
江西银山矿区黄铁矿的标型特征研究   总被引:1,自引:0,他引:1  
银山矿区黄铁矿有七个世代,其中与矿化密切的为3-6世代,随着矿化的演化,黄铁矿中硫相对减少,砷相对增高。银山黄铁矿微量元素以高As、Te,低Se、Co、Ni,且Se/Te<1,Co/Ni<1为特征,黄铁矿的稀土元素配分型式与矿区火山岩一次火山岩相一致  相似文献   
66.
As a result of the collapse of a mine tailing dam, a large extension of the Guadiamar valley was covered with a layer of pyritic sludge. Despite the removal of most of the sludge, a small amount remained in the soil, constituting a potential risk of water contamination. The kinetics of the sludge oxidation was studied by means of laboratory flow-through experiments at different pH and oxygen pressures. The sludge is composed mainly of pyrite (76%), together with quartz, gypsum, clays, and sulphides of zinc, copper, and lead. Trace elements, such as arsenic and cadmium, also constitute a potential source of pollution. The sludge is fine grained (median of 12 μm) and exhibits a large surface (BET area of 1.4±0.2 m2 g−1).

The dissolution rate law of sludge obtained is r=10−6.1(±0.3) [O2(aq)]0.41(±0.04) aH+0.09(±0.06) gsludge m−2 s−1 (22 °C, pH=2.5–4.7). The dissolution rate law of pyrite obtained is r=10−7.8(±0.3) [O2(aq)]0.50(±0.04) aH+0.10(±0.08) mol m−2 s−1 (22 °C, pH=2.5–4.7). Under the same experimental conditions, sphalerite dissolved faster than pyrite but chalcopyrite dissolves at a rate similar to that of pyrite. No clear dependence on pH or oxygen pressure was observed. Only galena dissolution seemed to be promoted by proton activity. Arsenic and antimony were released consistently with sulphate, except at low pH conditions under which they were released faster, suggesting that additional sources other than pyrite such as arsenopyrite could be present in the sludge. Cobalt dissolved congruently with pyrite, but Tl and Cd seemed to be related to galena and sphalerite, respectively.

A mechanism for pyrite dissolution where the rate-limiting step is the surface oxidation of sulphide to sulphate after the adsorption of O2 onto pyrite surface is proposed.  相似文献   

67.
This paper describes coal petrographic characteristics, sulfur abundance, distribution and isotopic signature in coals in the Wuda coalfield, Inner Mongolia, northern China. Petrographic studies suggest that depositional environment influences petrographic composition. The No. 9 and No. 10 coal seams, which are thought to have formed on a tidal delta plain, have high collodetrinite contents (up to 66.1%) indicating enhanced gelification and bacteria activity during coal accumulation, and also have the highest sulfur content (3.46% and 3.42%). Both organic and pyritic sulfur isotope values (−12.3‰ to 5.8‰ and −18.7‰ to 1.1‰, respectively) are variable and generally tend to be more negative in high-sulfur coals than those in low-sulfur coals in the Wuda coalfield. The negative sulfur isotope values indicate that a large portion of sulfur in the high-sulfur coals has a bacterial origin. Sulfur isotopic compositions and variations within the section were used to propose a model to explain the origin of sulfur in these coals. The presence of pyritized rod-like bacteria, cyanophyte's gelatinous sheaths and degraded algae organic matter suggests that bacteria, and perhaps algae, may play an important role in the formation of these high-sulfur coals.  相似文献   
68.
 The assessment of the aluminosilicate buffering potential during acid weathering of the Estonian alum shale is provided. It is found that the stoichiometric interaction between dissolved pyrite oxidation products and illite of the shale best describe the buffering process and are consistent with earlier field studies. The scheme includes incongruent dissolution of illite with smectite and K-jarosite precipitating. This complex mechanism involves buffering of 8% of the acidity by K+ and temporary precipitation of 25% of the acidity as K-jarosite. Dissolution proceeds at a low pH (1.5–3) until all pyrite in the shale particle is oxidised. Hence, if the total amount of illite present is larger than needed for stoichiometric interactions, only part of it is involved in a buffering process, neutralising a certain percentage of acidity. The next stage in shale weathering is the incongruent dissolution of K-jarosite with the release of the precipitated acidity and the formation of ferric oxyhydroxide. Received: 3 August 1998 · Revised paper: 26 January 1999 · Accepted: 23 February 1999  相似文献   
69.
西南三江地区镇沅金矿载金黄铁矿稀土与微量元素特征   总被引:5,自引:1,他引:4  
赵岩  黄钰涵  梁坤  张岐能 《岩石学报》2015,31(11):3297-3308
镇沅金矿(也称老王寨金矿)是西南三江地区哀牢山金矿带超大型金矿床之一。前人研究表明黄铁矿的稀土与微量元素含量可以反映成矿流体与成矿物质来源的特征,本次采用电感耦合等离子质谱仪(ICP-MS)技术对镇沅金矿主要载金矿物黄铁矿进行研究。通过野外实地调查及室内显微镜下观察,将镇沅金矿载金黄铁矿分为四个阶段:Ⅰ阶段脉状黄铁矿;Ⅱ阶段团块状黄铁矿;Ⅲ阶段与辉锑矿等硫化物共生浸染状黄铁矿;Ⅳ阶段破碎状黄铁矿。矿区内多种地层均有矿化现象,矿石类型包括变砂岩型、炭质板岩型、蚀变大理岩型、蛇绿岩套型、蚀变花岗岩型、煌斑岩型等。ICP-MS测定结果显示Ⅰ阶段黄铁矿富集高场强元素Th、U、Ta、Nb、Zr、Hf,亏损大离子亲石元素;其后三阶段黄铁矿该特征则不明显。黄铁矿总体稀土元素含量较低,∑REE含量为4.72×10-6~48.96×10-6,平均为24.93×10-6。稀土配分曲线显示黄铁矿总体呈较平缓的右倾型轻稀土元素富集配分模式;存在负δEu异常,基本无δCe异常。各阶段黄铁矿稀土配分模式存在微弱差异,Ⅰ阶段黄铁矿总体REE含量较高,部分具有LREE/HREE比值较低的特征,与超基性岩REE配分模式相近;Ⅱ阶段黄铁矿REE含量明显偏低,LREE/HREE比值较高;Ⅲ阶段黄铁矿∑REE含量较低,但较Ⅱ阶段要高;Ⅳ阶段黄铁矿∑REE含量低,有与Ⅱ阶段黄铁矿REE相近特征。黄铁矿中Au与As伴生现象明显。Co/Ni值反映黄铁矿具有沉积与热液黄铁矿成因特征,另外黄铁矿的稀土微量元素特征还反映出成矿流体为含F-的还原性流体。研究认为镇沅金矿至少存在两期金成矿作用,早期载金黄铁矿呈脉状产出,并可能与印支期古特提斯洋闭合中含超基性岩的增生楔形成有关;晚期载金黄铁矿与辉锑矿、黄铜矿等硫化物共生,与新生代区域范围内红河剪切带活动及扬子板块的俯冲导致的广泛变质作用有关。  相似文献   
70.
哈图金矿蚀变岩型矿体特征及金赋存状态研究   总被引:1,自引:0,他引:1  
哈图金矿由石英脉型和蚀变岩型矿体组成,蚀变岩型矿体遭受了强烈黄铁矿化、毒砂化、碳酸盐化、硅化和绢云母化蚀变.成矿作用划分5个阶段:钠长石-石英阶段(I)、黄铁矿-碳酸盐-石英阶段(II)、黝铜矿-黄铜矿-自然金阶段(III)、毒砂-碳酸盐-绢云母阶段(IV)和方解石-石英阶段(V).其中,II—IV阶段是主要金成矿阶段.哈图金矿含金矿物主要为自然金,平均成色912.自然金呈裂隙金、包裹金、粒间金形式嵌布在黄铁矿和毒砂中.当载金矿物为黄铁矿时,自然金与黝铜矿-黄铜矿-闪锌矿关系密切;当载金矿物为毒砂时,自然金与黄铁矿-黄铜矿关系密切.  相似文献   
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