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991.
伏牛山构造带变质流体脉变形特征及构造意义   总被引:1,自引:0,他引:1       下载免费PDF全文
伏牛山构造带由多条近平行的断裂带和夹持其间的变形岩片组成,洛南-栾川断裂带和瓦穴子-乔端断裂带为其中的两条主要断裂带。这两条断裂带虽遭受多期强烈构造活动的影响,但主造山期的构造特征至今仍然保存完好,并以中深层次的韧性剪切变形为主,形成了典型的糜棱岩和同构造期石英脉。本文从宏观、微观、超微观变形特征及年龄等方面对这些变质流体脉进行了研究,以探讨与其形成密切相关的构造活动特征、年代及其在秦岭造山带和华北板块南缘强变形带中的作用。石英脉中石英颗粒动态重结晶特征总体显示远离剪切带只有少量的膨凸式,靠近断裂带为亚颗粒式,形成核-幔结构,位错特征显示远离剪切带位错密度较小,靠近断裂带较大,位错形态显示瓦乔断裂带以挤压为主,洛南-栾川断裂带以剪切为主。两条断裂带石英脉的变形特征说明它们的糜棱岩化过程均为塑性变形中的晶质塑性变形,形成过程均为挤压在先,剪切在后。所测糜棱岩中石英脉的ESR年龄分别为372.9±30.0 Ma、275.0±20.0 Ma和218.0±20.0 Ma,真实地记录了晚加里东至中-晚海西期北秦岭的构造活动及所受影响。其中372.9±30.0 Ma是宽坪岩块向华北板块下的斜向俯冲汇聚和走滑的年代, 275.0±20.0 Ma是瓦乔断裂带的形成年龄。218.0±20.0 Ma的年龄则反映了华南、华北两大板块印支晚期全面闭合作用在秦岭造山带内部的影响。从以上3个年龄可以看出:北秦岭各构造带自北向南演化,时代上自北向南变新。  相似文献   
992.
Within the Pilbara Block of Western Australia, a complex of migmatite, gneissic and foliated granite near Marble Bar is intruded by a stock of younger massive granite (the Moolyella Granite) with which swarms of tin‐bearing pegmatites are associated. The age of the older granite has been determined by the Rb‐Sr method as 3,125 ± 366 m.y., and that of the Moolyella Granite as 2,670 ± 95 m.y. Initial Sr87/Sr86 ratios suggest that the older granite is close to primary crustal material, but that the Moolyella Granite consists of reworked material. It probably formed by partial remelting of the older granite.  相似文献   
993.
Tabular steeply dipping cassiterite‐bearing lodes in the Mount Wells region are hosted by lower greenschist fades metasediment of the Pine Creek Geosyncline within the contact aureole of late orogenic granitoids. The latter are predominantly I‐type, but S‐type phases are developed near the sediment‐granitoid contact.

Quartz, cassiterite, pyrite, arsenopyrite, chalcopyrite and pyrrhotite are the main minerals. Two types of lodes are present: (i) Sn‐quartz lodes containing 5–10 vol% sulphide minerals; and (ii) Sn‐sulphide lodes containing ~ 70 vol% sulphide minerals. At the surface, the former appear as normal quartz veins and the latter as hematite‐quartz breccia resulting from the collapse of original sulphide‐rich lodes as a consequence of volume reduction due to oxidation and leaching.

Two stages of quartz veining are recognized in both types of lodes. Cassiterite is present in stage I while stage II is composed of barren quartz with minor pyrite. Late stage III carbonate veinlets are present in Sn‐sulphide lodes. The lode‐wallrock contact is sharp with weak alteration effects confined to the fringe of the lodes. The alteration minerals include sericite, quartz, tourmaline, chlorite, pyrite and minor K‐feldspar.

Four types of fluid inclusions are present in vein quartz and cassiterite: Type A (CO2 ± H2O ± CH4); Type B (H2O+~ 20% vapour); Type C (H2O+ < 15% vapour) and Type D (H2O+ < 15% vapour + NaCl). Early ‘primary’ inclusions represented by Types A and B are present in stage I only and have a well‐defined temperature mode at ~300°C and a salinity range of 1–20 wt% eq NaCl. Types C and D inclusions are ‘secondary’ in stage I and primary in stage II and have a temperature mode at 120–160°C and salinities from about 1 to more than 26 wt% eq NaCl. Variable H2O‐CO2 ratios of Type A inclusions and homogenization in CO2 or H2O phase at near identical temperature indicate entrapment at the H2O‐CO2 solvus and define a pressure of ~ 100 MPa. The melting sequence of frozen inclusions suggests that the ore fluids were mainly H2O‐CO2‐CH4‐Na‐Ca‐Cl brines. This is also confirmed by Raman Laser Spectrometry.

Oxygen and sulphur isotope data are consistent with a magmatic origin of the ore fluids. The δD values are up to 20%0 higher than those expected for magmatic fluids and probably resulted from interaction of the latter with the carbonaceous strata. This interpretation is supported by δ13C data on the fluid inclusion CO2.

Fluid inclusions, stable isotope and mineralogical data are used to approximate the physico‐chemical parameters of the ore fluids which are as follows: T 300°C, m Cl~2, fO2 ~ 10‐35, mSS ~ 0.01, Sn ~ 1 ppm, Cu ~ 1 ppm and pH ~ 5.5.

It is suggested that fluids of granitic parentage interacted with the enclosing sediment and picked up CO2, CH4 and possibly Ca. The granitic phases became reduced due to this interaction and developed S‐type characteristics. Tin was probably partitioned into the CH4‐bearing reduced fluids. At some stage the fluid overpressure exceeded the lithostatic lode enforcing failure of the carapace and the intruded rocks by hydraulic fracturing causing CH4 and CO2 loss resulting in the precipitation of the ore minerals.  相似文献   
994.
Skarns are developed over two temperature‐time intervals in calcite limestone adjacent to the southern extension of the Glenrock Granodiorite, a pluton of the Marulan Batholith, Southern Highlands, New South Wales. The initial volumetrically‐dominant prograde phase of skarn formation produced a suite comprising bimetasomatic skarn, including pyroxene endoskarn, potassic endoskarn and wollastonite‐bearing exoskarn, together with mineralogically‐zoned vein skarn, massive garnet‐pyroxene skarn and calcite‐vesuvianite skarn. Retrograde replacement is manifested by the development of hydrous silicate minerals, carbonate and cross‐cutting sulphide veinlets.

A genetic model is proposed to account for the development of bimetasomatic skarn in the deposit. Exoskarn geochemistry indicates addition of many components relative to an essentially pure limestone precursor, including Si, Al, Fe, Zr, Zn, S, Mn and Cu, negligible transfer of K, Na and Rb and loss of CO2. Strontium and Ca loss from the parent limestone is indicated by mass balance calculations at constant volume.

Garnet and pyroxene compositions in the massive garnet‐pyroxene skarn range from Gr30 to Gr66 and Hd61 to Hd87, respectively. Compositions from Gr67 to Gr95 are typical of the vein skarn garnets. Chemical zonation patterns in garnet, pyroxene and vesuvianite are generally characterized by rim Fe depletion relative to cores of grains.

Prograde skarn probably formed at T = 500–580°C; P < 220 MPa. The massive garnet‐pyroxene skarn evolved under conditions of log fO2 = ‐18.9 to ‐22.9 (assuming a constant fCO2 of 20 MPa) within the fS2 stability field of pyrrhotite. Retrograde skarn formed at T < 400°C, possibly under conditions of XH2O < 0.01.

Vesuvianite plus wollastonite assemblages, present in exoskarn, probably attest to very water‐rich conditions. The marble wall rocks, isolated from the source of skarn‐forming fluids, probably evolved under conditions of minimum Xco2 >0.2. Low temperature CO2 ‐rich fluid inclusions and prehnite (stable at Xco2 <0.01), present in the marble and skarn, respectively, suggest that substantial differences in Xco2: XH2O were maintained during cooling.

Observed mineralogical and chemical zonation within the skarn reflects the complex interaction of T, P, fO2, Xco2 and other chemical variables such as aSiO2 and aAl2O3 throughout the skarn system. No single variable can account adequately for the mineralogical diversity observed in the skarn deposit.  相似文献   
995.
The Pb–Zn deposit at Jebel Ghozlane, in the Nappe zone (northern Tunisia), is hosted by Triassic dolostones and Eocene limestones and is located along faults and a thrust‐sheet boundary. The sulfide mineralization of the deposit consists mainly of galena and sphalerite and occurs as vein, stockwork, breccia, dissemination and replacement ores. Three hydrothermal stages are involved in the formation of the ores: stage I is dominated by celestite‐barite, hydrothermal dolomite DII, colloform sphalerite, and galena I; stage II consist of galena II; and stage III contains calcite. Galena in the deposit yielded average 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of 18.705, 15.667 and 38.734, respectively, suggesting a single upper crustal source reservoir for metals. Trace element data indicate the presence of Zn‐ and As‐free galena and As‐rich galena (with 0.2–0.5% As). Sphalerite contains 0.4% As, 0.7–0.9% Cd and 0.1–1.5% Fe. Microthermometric analysis of fluid inclusions in celestite shows that the deposit formed from fluids composed of heterogeneous mixtures of saline (19.5 ± 1 wt% NaCl eq.) aqueous solutions sourced from basinal brines, and gaseous CO2‐rich phases bearing low amounts of CH4, N2 and/or H2S, at temperatures of 172 ± 5°C.  相似文献   
996.
宋家营勘查区位于河北唐山丰南区,存在着新生界厚度大,流沙层、卵石层、砂砾层松散破碎,部分钻孔漏失严重;煤层埋藏深、层数多、层位变化大等问题,给提高钻探施工质量和效益带来了不便。为解决这些问题,作者从钻孔设计人手,针对不同的地层采用相适应钻探工艺和技术措施,对长期沿用钻探方法进行改进,使钻进方法更具有针对性;对不同的地层配制了不同的冲洗液,对地层漏失根据情况采用恰当的堵漏方法,大大减少了因堵漏增加的成本。从而使钻进效率由过去的287m/台月,提高到440m/台月,台月效率提高了53.3%,大大降低了钻探成本。  相似文献   
997.
木里煤田属高寒缺氧地区,冻土(岩)层在钻进中遇热融解、融化,从而使孔内出现大范围的坍塌,造成卡钻、埋钻事故频发,给钻探施工及岩煤心采取带来很大的困难。从钻孔结构设计、钻具选择、低温冲洗液配置等方面进行深入研究,总结出来了一套适用于木里煤田永久冻土地层的钻探技术。应用表明,该项技术将钻月效率从2004年的224m,提高到2006年的424.5m,效果显著。  相似文献   
998.
河南省新县姚冲钼矿床流体包裹体研究   总被引:1,自引:1,他引:0  
河南省新县姚冲钼矿床产于大别造山带,属于陆-陆碰撞体制的斑岩型矿床,其流体成矿过程可以分为早、中、晚三个阶段,分别以石英+钾长石±黄铁矿±磁铁矿、石英±钾长石+辉钼矿±其他硫化物和石英±碳酸盐±萤石组合为标志.热液石英和萤石中发育纯CO2包裹体(PC型)、CO2-H2O型包裹体(C型)、水溶液包裹体(W型)和含子晶多相包裹体(S型).早阶段石英中发育纯CO2包裹体、CO2-H2O型包裹体和含子晶多相包裹体,中阶段的石英则发育CO2-H2O型包裹体、水溶液包裹体和含子晶多相包裹体,在晚阶段的无矿石英脉中发育水溶液包裹体和少量的CO2-H2O型包裹体,石英-碳酸盐-(萤石)脉石英与萤石中只发育水溶液包裹体.早阶段流体包裹体的均一温度为277~ 380℃,集中于300~ 360℃,盐度变化于3.0%~10.3% NaCleqv之间.中阶段包裹体均一温度介于185 ~ 351℃之间,集中在260~ 320℃,盐度介于2.4% ~9.3%NaCleqv;晚阶段包裹体均一温度为139 ~245℃,盐度介于0.7% ~6.3% NaCleqv之间.中阶段多相包裹体中常见黄铜矿和其他透明子矿物,表明流体具有还原性、过饱和的特征,是矿石矿物沉淀的主要阶段.估算早、中阶段流体捕获压力分别集中于47 ~ 131MPa和26 ~118MPa,所对应的成矿深度分别约为4.7km和2.6~4.2km.上述流体包裹体的研究表明姚冲钼矿床的初始成矿流体具有高温、高盐度、富CO2的特征,同时预测了深部找矿潜能.  相似文献   
999.
新疆阿尔泰塔拉特铁铅锌矿床流体包裹体研究及矿床成因   总被引:4,自引:1,他引:3  
李登峰  张莉  郑义 《岩石学报》2013,29(1):178-190
塔拉特铁铅锌矿位于新疆阿尔泰造山带南缘的阿巴宫多金属成矿带,矿体赋存于克兰盆地下泥盆统康布铁堡组中,为一套海相中酸性火山岩-火山碎屑岩、陆源碎屑沉积岩-碳酸盐岩建造,脉状矿体受阿巴宫大断裂次级断裂控制.根据矿物组合和脉体穿插关系,塔拉特铁铅锌矿可分为4个成矿阶段:矽卡岩,氧化物,硫化物和碳酸盐阶段,后3个阶段均有石英共生.其中,硫化物(方铅矿-闪锌矿±磁黄铁矿±黄铜矿)阶段是铅锌成矿的主要阶段.不同阶段石英中广泛发育流体包裹体,可分为水溶液包裹体(W型)、纯CO2包裹体(PC型)、CO2-NaCl-H2O包裹体(C型)及含子矿物多相包裹体(S型)4类.冷热台显微测温和激光拉曼分析表明,氧化物阶段石英含有4种类型的包裹体,以W型为主,C型和S型包裹体次之,包裹体均一温度介于271~ 426℃,W型和C型盐度范围0.5%~22.4% NaCleqv,S型包裹体盐度30.5% ~40.6% NaCleqv;硫化物阶段的石英流体包裹体为W型、C型和PC型,均一温度为204 ~ 269℃,盐度介于0.2%~15.6% NaCleqv之间;碳酸盐阶段的矿物只含W型包裹体,均一温度集中在175~211℃之间,盐度为1.1% ~9.9% NaCleqv.利用C型包裹体对硫化物阶段成矿压力估算,得到107 ~ 171MPa,对应深度为4~6km.塔拉特铁铅锌矿初始成矿流体具有高温、高盐度、富CO2的特征,但碳酸盐阶段低盐度、贫CO2,流体不混溶和混合作用导致了成矿物质的沉淀.塔拉特铁铅锌矿的地质和成矿流体特征显示其为碰撞造山体制形成的矽卡岩型成矿系统.  相似文献   
1000.
为研究利津洼陷沙四上亚段深部砂岩成岩环境,对岩心样品进行偏光、荧光、阴极发光显微镜和扫描电镜观察,辅以粘土矿物含量、元素含量测试.识别出酸性和碱性2种成岩环境,酸性环境以硅质沉淀、碳酸盐矿物溶解、长石溶解或蚀变为高岭石等现象组合为标志,碱性环境以碳酸盐矿物沉淀、长石次生加大、石英溶解等现象组合为标志.总体演化为:同生期,原始沉积流体造成碱性环境;早成岩期,未熟有机质演化形成短期的酸性环境,继承流体形成主体的碱性环境;中成岩A1期(埋深约2700~3200m),有机质成熟形成酸性环境;中成岩A2期(埋深约3200~4200m),深部断裂活动形成碱性环境;中成岩B期(埋深约4200~4400m),第二期充注油气的热演化形成酸性环境.  相似文献   
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