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41.
含水矿物在真空下的释Ar机制:Ar-Ar热年代学面临的新问题   总被引:2,自引:0,他引:2  
马芳  穆治国 《地学前缘》2002,9(2):505-510
地质体的实际情况、激光显微探针束研究、XRD和SEM观测以及真空加热下Ar的释放特征都表明体积扩散不是含水矿物在真空加热中释放Ar的唯一机制。在低温下 ,Ar的释放主要受由缺陷引起的短程扩散和体积扩散共同作用的多途径扩散机制制约 ;而在高温下 ,由于含水矿物在真空中不够稳定 ,Ar的释放受到脱羟基、脱氢、氧化反应、分层作用等造成的晶体结构改变的强烈影响。含水矿物在高温下的氧化分解会导致矿物中原始Ar浓度梯度的均一化 ,因而无法得到真实的Ar分布剖面 ,也无法据此计算矿物的封闭温度 ,并进而可能影响到ArAr年龄坪的地质意义。  相似文献   
42.
Trevor H. Green  John Adam 《Lithos》2002,61(3-4):271-282
The solubility of Ti- and P-rich accessory minerals has been examined as a function of pressure and K2O/Na2O ratio in two series of highly evolved silicate systems. These systems correspond to (a) alkaline, varying from alkaline to peralkaline with increasing K2O/Na2O ratio; and (b) strongly metaluminous (essentially trondhjemitic at the lowest K2O/Na2O ratio) and remaining metaluminous with increasing K2O/Na2O ratio (to 3). The experiments were conducted at a fixed temperature of 1000 °C, with water contents varying from 5 wt.% at low pressure (0.5 GPa), increasing through 5–10 wt.% at 1.5–2.5 GPa to 10 wt.% at 3.5 GPa. Pressure was extended outside the normal crustal range, so that the results may also be applied to derivation of hydrous silicic melts from subducted oceanic crust.

For the alkaline composition series, the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure but is unchanged with increasing K content (at fixed pressure). The P2O5 content of the alkaline melts at apatite saturation increases with increased pressure at 3.5 GPa only, but decreases with increasing K content (and peralkalinity). For the metaluminous composition series (termed as “trondhjemite-based series” (T series)), the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure and with increasing K content (at fixed pressure). The P2O5 content of the T series melts at apatite saturation is unchanged with increasing pressure, but decreases with increasing K content. The contrasting results for P and Ti saturation levels, as a function of pressure in both compositions, point to contrasting behaviour of Ti and P in the structure of evolved silicate melts. Ti content at Ti-rich mineral saturation is lower in the alkaline compared with the T series at 0.5 GPa, but is similar at higher pressures, whereas P content at apatite saturation is lower in the T series at all pressures studied. The results have application to A-type granite suites that are alkaline to peralkaline, and to I-type metaluminous suites that frequently exhibit differing K2O/Na2O ratios from one suite to another.  相似文献   

43.
Abstract: A strange, unidentified, Cu-Fe bearing zinc sulfide occurs in the Laloki massive sulfide deposit, Papua New Guinea. The mineral is optically uniform in texture but is chemically variable and zoned even within a single grain. Copper contents vary from 0.1 up to 8.85 wt%. Iron reaches 18.31 wt% at maximum and decreases as Cu increases. It is remarkable, however, that the total Fe+Cu remains essentially unchanged between roughly 18 and 20 wt%. Zn and S are least variable, giving 45.85–47.84 wt% and 33.48–34.58 wt%, respectively. Other trace elements such as Cd and Mn are in general less than 0.2 wt%. It is strongly suggested that the mineral in question constitutes a unique Fe-Cu substitutional solid solution series belonging essentially to the Zn–Fe–Cu–S system.
The ideal chemical formula of the solid solution series can well be presented as Zn10(Fe, Cu)5S15 or Zn2(Fe, Cu)S3, where Fe is always greater than Cu. It is intriguing that chalcopyrite blebs are recognizable restrictively only in nearby portions of the Cu-rich end member with the ideal composition close to Zn10Fe3Cu2S15. It has been confirmed by vacuum-sealed heating experiments that this mineral is decomposed to produce chalcopyrite and Fe-bearing normal sphalerite at temperatures below 200C. This would provide another evidence for the existence of such distinct phase as suggested here.  相似文献   
44.
Cu-poor meneghinite from La Lauzière Massif (Savoy, France) has the composition (electron microprobe) (in wt%): Pb 59.50, Sb 20.33, Bi 1.19, Cu 0.87, Ag 0.05, Fe 0.03, S 17.62, Se 0.05, Total 99.64. Its crystal structure (X-ray on a single crystal) was solved with R1=0.0506, wR2=0.1026, with an orthorhombic symmetry, space group Pnma, and a=24.080(5) Å, b=4.1276(8) Å, c=11.369(2) Å, V=1130.0(4) Å3, Z=4. Relatively to the model of Euler and Hellner (1960), this structure shows a significantly lower site occupancy factor for the tetrahedral Cu site (0.146 against 0.25). Among the five other metallic sites, Bi appears in the one with predominant Sb. Developed structural formula: Cu0.15Pb2(Pb0.53Sb0.47)(Pb0.46Sb0.54)(Sb0.75Pb0.19Bi0.06)S6; the reduced one: Cu0.58Pb12.72(Sb7.04Bi0.24)S24. The formation of such a Cu-poor variety seems to be related to specific paragenetic conditions (absence of coexisting galena), or to crystallochemical constraints (minor Bi). To cite this article: Y. Moëlo et al., C. R. Geoscience 334 (2002) 529–536.  相似文献   
45.
46.
阿尔泰可可塔勒铅锌矿床围岩蚀变及成因   总被引:2,自引:3,他引:2  
姜俊 《矿产与地质》2003,17(6):679-682,734
可可塔勒铅锌矿床受火山喷发中心和沉积洼地控制,铅锌沉淀于海进阶段的局限还原卤水池中;矿下存在大型蚀变带,构成成矿流体对流循环过程中的水-岩作用带;后期造山挤压过程使地层和矿体倒转,矿床最终定位于麦兹倒转向斜之北东倒转翼的东南近转折部位。指出该矿床属海底火山喷流沉积改造型块状硫化物铅锌矿床。  相似文献   
47.
An isochron age of 282±20 (95% conf. limit) Ma of the sulfide ores in the Huangshandong Cu-Ni sulfide deposit, the East Tianshan Mountains has been obtained through Re-Os isotopic measurement. The age implies that the Cu-Ni sulfide deposit and other related deposits in the same area occurred in a Permian extensional environment of post-collision instead of Devonian-Early Carboniferous ophiolite-related oceanic or island arc environments inferred before. It shares the same ages with the orogenic and epithermal gold deposit systems in the same area. An initial 187Os/188Os ratio of 0.25±0.04 (1σ) and a γos value of 99 on average display the participation of large quantities of crustal components into the rock-forming and ore-forming system during mineralization and magmatic emplacement.  相似文献   
48.
胶东金矿床碳酸盐矿物的碳-氧和锶-钕同位素地球化学研究   总被引:16,自引:8,他引:16  
对胶东四类金矿床(盆地边缘砾岩型、斑岩型-浅成热液型、石英脉型和破碎带蚀变岩型)矿石中的碳酸盐矿物开展了系统的碳-氧同位素和锶-钕同位素地球化学研究。研究结果表明,与宏观的成矿地质条件和矿床地质特征相对应,山东金矿床可能有亲岩浆岩和亲沉积盆地两个不同的成矿系统。前者包括斑岩型-浅成热液型、石英脉型和破碎带蚀变岩型三类金矿床,后者指盆地边缘砾岩型金矿床,二者具有不同的碳-氧和锶-钕同位素地球化学特征。山东亲岩浆岩系列的金矿床,其锶-钕同位素与同时代的幔源岩浆岩一致,碳同位素显示幔源碳和岩浆碳的特征,氧同位素则显示初生水与大气降水不同比例混合的可能性,因此有可能是以CO2为主、富合成矿金属的地幔流体与浅部下渗大气降水相互作用的结果。而与岩浆岩关系不密切、主要受盆地边缘断裂控制的盆地边缘砾岩型金矿床,其碳-氧和锶-钕同位素组成均较分散,可能主要与地壳浅部下渗大气降水对上地壳各种岩石淋滤萃取演化而成的成矿流体有关。  相似文献   
49.
区内砂岩中的粘土矿物主要是自生的高岭石、绿泥石和伊蒙混层,而泥岩中的粘土矿物是伊蒙混层和高岭石,少量绿泥石。未见蒙脱石。砂岩和泥岩中粘土矿物的转化具有相似的水介质和地温条件,都反映出在中—晚成岩期形成,而且与烃类的排出和运移密切相关。泥岩中粘土矿物转化和脱水作用为砂岩输送流体和释放溶解物质。而且泥岩中有机质的脱羟基向砂输送酸性水,促进砂岩中骨架颗粒溶解、次生孔隙的产生。  相似文献   
50.
多孔结构矿物(岩石)及其环境修复材料的实用性   总被引:12,自引:1,他引:12       下载免费PDF全文
具有多孔结构的矿物(岩石)作为一类特殊的工业原材料,在环境修复领域的应用前景正在成为研究热点。本文从微孔的尺度、结构、形态、成分等表面固体特征出发,概括性地论述了凹凸棒石、海泡石、蒙脱石、沸石、硅藻土等十几种多孔结构矿物(岩石)在环境修复工程中用作过滤材料、吸附剂、离子交换剂和催化剂等材料时的基本特征和使用时应注意的问题。  相似文献   
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