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1.
地幔岩中流体包裹体研究   总被引:5,自引:2,他引:3  
卢焕章 《岩石学报》2008,24(9):1954-1960
地幔岩石中的流体包裹体代表地幔流体的样品。地幔流体包裹体可以存在从地幔来的金刚石,地幔捕虏体和岩浆碳酸岩中。研究这些岩石和矿物中的流体包裹体可以得出其所代表的地幔流体的温度、压力、成分和同位素。我们目前见到的这三类地幔岩石的包裹体主要可在橄榄石、辉石、金刚石、方解石和磷灰石中见到。这些包裹体可以粗略地分为CO2包襄体和硅酸盐熔融体包裹体。又可细分为四类包裹体:(1)富碳酸盐的硅酸盐熔融包裹体。这种包裹体在金刚石、地幔岩捕虏体和岩浆碳酸盐岩中见到,它又可分为结晶质熔融包裹体和玻璃包裹体。(2)CO2包裹体。这种包裹体大多见于地幔捕虏体中,在金刚石和岩浆碳酸岩中也可见到。(3)含硫化物的包裹体。这种包裹体见于地幔捕虏体中,与纯CO2包裹体和含CO2的熔融包裹体共存。(4)高密度的流体包裹体。这种包裹体见于金刚石中,是一种高盐度、高密度的含K、Cl和H2O的流体包裹体,又可分为高卤水包裹体和含卤水的富硅的碳酸盐岩浆包裹体。从对金刚石、地幔捕虏体和岩浆碳酸盐岩中流体包裹体的研究表明,地幔流体存在不均匀性和不混溶性。  相似文献   
2.
A combination of CTD casts, discrete bottle sampling and in situ voltammetric microelectrode profiling was used to examine changing redox conditions in the water column at a single station south of the Bay Bridge in the upper Chesapeake Bay in late July/early August, 2002–2005. Short-term (2–4 h) fluctuations in the oxic/suboxic/anoxic interface were documented using in situ voltammetric solid-state electrodes. Profiles of dissolved oxygen and sulfide revealed tidally-driven vertical fluctuations of several meters in the depth and thickness of the suboxic zone. Bottom water concentrations of sulfide, Mn2+ and Fe2+ also varied over the tidal cycle by approximately an order of magnitude. These data indicate that redox species concentrations at this site varied more due to physical processes than biogeochemical processes. Based on analysis of ADCP data, tidal currents at this station were strongly polarized, with the principal axis of tidal currents aligned with the mainstem channel. Together with the chemical data, the ADCP analysis suggests tidal flushing of anoxic bottom waters with suboxic water from north of the site. The present study is thus unique because while most previous studies have focused on processes across relatively stable redox interfaces, our data clearly demonstrate the influence of rapidly changing physical mixing processes on water column redox chemistry.Also noted during the study were interannual differences in maximum bottom water concentrations of sulfide, Mn2+ and Fe2+. In 2003, for example, heavy spring rains resulted in severe hypoxia/anoxia in June and early July. While reported storm-induced mixing in late July/early August 2003 partially alleviated the low-oxygen conditions, bottom water concentrations of sulfide, Mn2+ and Fe2+ were still much higher than in the previous year. The latter implies that the response time of the microbial community inhabiting the suboxic/anoxic bottom waters to changing redox conditions is slow compared to the time scale of episodic mixing events. Bottom water concentrations of the redox-sensitive chemical species should thus be useful as a tracer to infer prior hypoxic/anoxic conditions not apparent from ambient oxygen levels at the time of sampling.  相似文献   
3.
Zinc–lead–barite deposits located in Lefan and Lower Banik localities of about 25 km northeast of Zakho City, Northern Iraq consist of a group of strata-bound sulfides hosted in Upper Cretaceous (Upper Campanian–Maastrichtian) dolomitic limestone. Carbonate-hosted ores contain 3.77% Zn, 2% Pb, and 5% Fe, while in lower Banik, they contain 1.5% Zn, 0.37% Pb, and 1.4% Fe. Diagenetic processes, such as dolomitization and recrystalization in addition to the type of microfacies, provided appropriate physical and chemical conditions that permitted the passage of ore-bearing fluids and participated in precipitation and ore localization. These deposits are precipitated in a platform and developed within the Foreland Thrust Belt. Ore precipitated as infill of intergranular dolomite porosity with replaced dolomite and rudist shells forming disseminated crystals that occupy intergranular pore spaces around dolomite and calcite and as infill of dissolution spaces and fractures.  相似文献   
4.
Because of the high degree of automation in the coal mining industry in the Ruhr area, Germany, about 1 metric ton of crushed rock/colliery spoil is brought to the surface for every metric ton of coal. Most of the colliery spoil disposed of must be dumped. These colliery spoil dumps are anthropogenic geological sediment bodies, which have a characteristic facies resulting from geological, technical, and economical factors connected with the formation of the dumps. The relation between the facies of the dumps and these factors, for example, is examplified with the pyrite content within the colliery spoil. Pyrite content within the dumps is dependent both on the conditions during sedimentation and (early) diagenesis and the techniques used for mining and processing. Thus, this geologic-technical facies of the dumps controls the weathering processes on and in dumps. These humaninduced processes are mainly responsible for the environmental impact on soil and groundwater. Oxidation of pyrite as well as alteration of pyrite under anoxic conditions yields dissolution of carbonates, accompanied by gypsum formation, by acid attack and strong acidification takes place.  相似文献   
5.
T. Kawakami  D.J. Ellis  A.G. Christy 《Lithos》2006,92(3-4):431-446
The high-temperature (HT) to ultrahigh-temperature (UHT) metamorphic rocks from Lützow–Holm Complex, East Antarctica show a systematic difference between sulfide assemblages in the rock matrix and those found as inclusions in the silicates stable in high-temperatures. Matrix sulfides are commonly pyrite with or without pentlandite and chalcopyrite. On the other hand, inclusion sulfides are pyrrhotite with or without pentlandite and chalcopyrite lamellae. When recalculated into integrated single-phase sulfide compositions, inclusion sulfides from the UHT region showed a wider range of solid–solution composition than the inclusion sulfides from the HT region. The host minerals of the sulfides with extreme solid–solution compositions are those stable at the peak of metamorphism such as orthopyroxene and garnet. One of the most extreme ones is included in orthopyroxene coexisting with sillimanite ± quartz, which is the diagnostic mineral assemblage of UHT metamorphism. These observations suggest that sulfide inclusions preserve their peak metamorphic compositions. Pyrrhotite did not revert to pyrite because of the closed system behavior of sulfur in inclusion sulfides. On the other hand, in the rock matrix where the open system behavior of sulfur is permitted, original sulfides were partly to completely altered by the later fluid activity.  相似文献   
6.
This study investigates the retention of heavy metals in secondary precipitates from a sulfidic mine rock dump and underlying podzolic soils by means of mineralogical and chemical extraction methods. The rock dump, which is at least 50 years old, consists of a 5–10-cm-thick leached zone and an underlying 110–115-cm-thick accumulation zone. Optical microscopy and electron microprobe analyses confirm that pyrrhotite weathering has proceeded much further in the leached horizon relative to the accumulation horizon. The weathering of sulfides in the leached zone has resulted in the migration of most heavy metals to the accumulation zone or underlying soils, where they are retained in more stable phases such as secondary ferric minerals, including goethite and jarosite. Some metals are temporarily retained in hydrated ferrous sulfates (e.g., melanterite, rozenite). Received: 28 October 1996 · Accepted: 24 February 1997  相似文献   
7.
Silicate and sulfide melt inclusions from the andesitic Farallón Negro Volcanic Complex in NW Argentina were analyzed by laser ablation ICPMS to track the behavior of Cu and Au during magma evolution, and to identify the processes in the source of fluids responsible for porphyry-Cu-Au mineralization at the 600 Mt Bajo de la Alumbrera deposit. The combination of silicate and sulfide melt inclusion data with previously published geological and geochemical information indicates that the source of ore metals and water was a mantle-derived mafic magma that contained approximately 6 wt.% H2O and 200 ppm Cu. This magma and a rhyodacitic magma mixed in an upper-crustal magma chamber, feeding the volcanic systems and associated subvolcanic intrusions over 2.6 million years. Generation of the ore fluid from this magma occurred towards the end of this protracted evolution and probably involved six important steps: (1) Generation of a sulfide melt upon magma mixing in some parts of the magma chamber. (2) Partitioning of Cu and Au into the sulfide melt (enrichment factor of 10,000 for Cu) leading to Cu and Au concentrations of several wt.% or ppm, respectively. (3) A change in the tectonic regime from local extension to compression at the end of protracted volcanism. (4) Intrusion of a dacitic magma stock from the upper part of the layered magma chamber. (5) Volatile exsolution and resorption of the sulfide melt from the lower and more mafic parts of the magma chamber, generating a fluid with a Cu/Au ratio equal to that of the precursor sulfide. (6) Focused fluid transport and precipitation of the two metals in the porphyry, yielding an ore body containing Au and Cu in the proportions dictated by the magmatic fluid source. The Cu/S ratio in the sulfide melt inclusions requires that approximately 4,000 ppm sulfur is extracted from the andesitic magma upon mixing. This exceeds the solubility of sulfide or sulfate in either of the silicate melts and implies an additional source for S. The extra sulfur could be added in the form of anhydrite phenocrysts present in the rhyodacitic magma. It appears, thus, that unusually sulfur-rich, not Cu-rich magmas are the key to the formation of porphyry-type ore deposits. Our observations imply that dacitic intrusions hosting the porphyry–Cu–Au mineralization are not representative of the magma from which the ore-fluid exsolved. The source of the ore fluid is the underlying more mafic magma, and unaltered andesitic dikes emplaced immediately after ore formation are more likely to represent the magma from which the fluids were generated. At Alumbrera, these andesitic dikes carry relicts of the sulfide melt as inclusions in amphibole. Sulfide inclusions in similar dykes of other, less explored magmatic complexes may be used to predict the Au/Cu ratio of potential ore-forming fluids and the expected metal ratio in any undiscovered porphyry deposit.Editorial handling: B. Lehmann  相似文献   
8.
Multi-isotope (H, O, S, Sr, Pb) systems coupled with conventional (major and trace element) hydrogeochemical analysis were applied to determine the origin of water, to model water-rock-tailings interactions and for source apportionment of sulfur and associated toxic metals in the mining region of Taxco, Guerrero in southern Mexico. Oxygen and H isotopes indicate that meteoric water in the zone is rainwater undergoing varying degrees of isotopic fractionation by atmospheric evaporation whereas Sr isotopes trace the interaction of pristine water from volcanics of the regional recharge zone and subsequently flowing through sandstone and shale to spring points. Leachates form from two distinctive sources (spring water and surface water) having differential interactions with bedrocks prior to entering the tailings. Compared to pristine water, leachates are enriched in sulfate, metals (e.g. Fe, Mn, Pb and Zn) and metalloids (e.g. As). The sulfur isotopic composition of ore-sulfides, leachates, secondary precipitates, regional surface water and hypogenic sulfates is described in terms of a two-component mixing model with shale of Mexcala and limestone of Morelos formations representing the light and heavy end-members, respectively, whereas Sr isotopic composition is bracketed combining three lithogenic (Mexcala/Morelos, Tilzapotla and Taxco Schist) sources. Finally, leachates have a mixture of lead from ore-sulfides and Taxco Schist Formation (Family I) or from ore-sulfides alone (Family II). The application of multiple environmental isotopic techniques is an outstanding tool for elucidating complex interactions of water with bedrocks and tailings and for determining the source of sulfur and toxic metal from mining and other metal polluted environments.  相似文献   
9.
王梦玺  陈炳龙  焦建刚 《岩石学报》2018,34(8):2223-2244
坡北杂岩体位于塔里木板块东北缘北山裂谷带,主要由橄榄岩相、单辉辉石岩相、二辉岩相、辉长岩相、苏长岩相和辉长苏长岩相组成。坡一岩体中硫化物矿体赋存于超镁铁质岩中,而坡东岩体中硫化物矿体赋存于辉长苏长岩相中。坡一和坡东岩体不同岩相中单斜辉石的MgO和CaO含量、斜长石的An值和SiO_2含量连续变化且呈负相关,说明二者可能是同一原始岩浆分离结晶的产物。根据前人计算的原始岩浆成分,我们利用MELTS软件模拟了坡北杂岩体的分离结晶过程。结果表明矿物结晶顺序为:橄榄石→橄榄石+单斜辉石→橄榄石+单斜辉石+斜长石→单斜辉石+斜长石+斜方辉石,与岩相观察一致。坡北杂岩体原始岩浆经过20%分离结晶达到S饱和而发生早期硫化物熔离,形成坡一岩体中矿体。因此,在利用具有最高Fo值(90.9mol%)的橄榄石成分进行的模拟中,坡一岩体早期结晶的纯橄榄岩中橄榄石成分与分离结晶趋势线一致,而斜长橄榄岩中橄榄石成分低于趋势线,可能形成于早期硫化物熔离之后。随后岩浆中S再一次不饱和,但坡一岩体橄榄单辉辉石岩和辉长岩中橄榄石Fo和Ni含量在分离结晶趋势线之下,同时坡东岩体不含矿岩石中铂族元素总量主要在8.9×10~(-9)~29.0×10~(-9)之间,且相对于Ni和Cu明显亏损,说明在岩浆分离结晶晚期再次发生硫化物熔离,而且可能是地壳混染引起的,并形成了坡东岩体中的硫化物矿体。坡东岩体橄榄二辉岩和橄榄辉长苏长岩中橄榄石Fo值(74.5mol%~81.0mol%)较低,但变化范围较大,且Fo和Ni呈负相关关系,这可能是由于橄榄石和硫化物熔体在不平衡状态下发生成分交换造成的。坡北杂岩体超镁铁质岩石中单斜辉石Ti O2含量为0.21%~0.83%,阳离子中呈四次配位的Al(AlZ)为0.8mol%~7.8mol%,与裂谷环境堆晶岩中单斜辉石成分相似。因此,坡北杂岩体可能形成于和塔里木二叠纪地幔柱活动相关的裂谷环境。然而,超镁铁质岩石全岩Nd同位素指示其来源于亏损地幔,并不是地幔柱物质熔融的直接产物。纯橄榄岩和异剥橄榄岩La/Sm,Sm/Yb和La/Yb比值指示其源区为尖晶石二辉橄榄岩地幔。因此,坡北杂岩体源区应为浅部以尖晶石二辉橄榄岩为主的亏损岩石圈地幔,地幔柱在源区部分熔融过程中提供了大量的热。  相似文献   
10.
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