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171.
付伟  赵芹  罗鹏  李佩强  陆济璞  周辉  易泽邦  许成 《地质学报》2022,96(11):3901-3923
传统认为中国南方的离子吸附型稀土矿床可划分为以“足洞式”为代表的重稀土型和以“河岭式”(或“花山式”)为代表的轻稀土型两种矿化类型。然而,近年来发现的许多矿床(如清溪、寨背和馒头山等)的赋矿风化壳中出现了轻稀土矿与重稀土矿并存现象,表现出特殊的“上轻下重”双层矿体结构。这指示了除重稀土型和轻稀土型之外,还存在着轻重稀土共生型的过渡类型。本研究通过对三种不同成矿类型的若干典型矿床系统对比,指出成矿类型的多样性与母岩性质密切相关,尤其是母岩的稀土元素地球化学和稀土载体矿物属性是制约成矿类型变化的关键因素。统计数据表明,从重稀土型→轻重稀土共生型→轻稀土型,成矿母岩的全岩稀土总量变化不大(ΣREY: 200×10-6~450×10-6→200×10-6~500×10-6→200×10-6~800×10-6),但轻重稀土配分值出现较显著的区间性差异(ΣLREE/ΣHREY: 02~1→1~5→2~10)。与之同时,母岩中能为离子相稀土提供物源且具有重稀土配分属性的稀土副矿物类型和数量明显减少,这与全岩稀土元素地球化学特征中重稀土分量占比的降低趋势也互相匹配。该结果指示,以往认为重稀土配分母岩形成重稀土矿床、轻稀土配分母岩形成轻稀土矿床的传统观点需要外延,即一部分具有低度轻稀土配分属性(1<ΣLREE/ΣHREY<5)且含有丰富易风化稀土副矿物的母岩还可能形成轻重稀土共生型矿床,该认识可为今后离子吸附型稀土矿床勘查工作提供新的找矿依据。  相似文献   
172.
本文从物探科学技术的进步,勘查任务的发展变化、物探方法应用范畴的扩大和物性勘探等几个方面,论述了岩石和矿物物理性质测量、研究的重要性,指出:物性工作不可能毕其功于一役,并提出了五点建议:1.深入研究各类矿藏及其围岩(直至地面)物性的空间变化规律,为选择、研究合适的物探方法,提高物探效果,进一步探讨“直接”找矿问题,提供依据;2.这项工作可专门进行,但最好尽可能利用为其他目的而设计的钻井进行;3.物  相似文献   
173.
扬子地台前寒武纪-寒武纪界线地层的微体植物化石群   总被引:10,自引:2,他引:8  
前寒武纪一寒武纪界线地层在扬子地台发育良好、分布广泛,并有包括微体植物群、海藻、瓶形原生物、具硬体动物及‘澄江动物群’等化石的发现。因而,扬子地台成为研究前寒武纪-寒武纪界线生物地层的代表地区之一。基于对扬子地台前寒武纪-寒武纪界线地层已知微体植物化石记录的回顾和论定,总结概括了下寒武统微体植物化石组合:寒武系最底部硅质磷块岩中的Micrhystridium-Paracymatiosphaera-Megathrix组合和较高层位页岩的Skiagia-Annulum-Archaeodiscina组合。它们分别与Anabarites-Circotheca-Protohertzina小壳动物化石带和Parabadiella及Eoredlichia三叶虫带相对应。与东欧地台疑源类生物地层相对照,扬子地台Micrhystridium-Paracymatiosphaera-Megathrix组合的纵向分布大体和东欧地台Asteridiumtornatum-Comasphaeridiumvelvetum组合带相一致,而以上两地台的化石组合产出层位可能都略高于纽芬兰东部剖面,依据Phycodespedum所厘定的寒武系底界?  相似文献   
174.
冀西北长城纪宣龙式铁矿层中微体植物化石的发现及其意义   总被引:10,自引:0,他引:10  
杜汝霖  刘志礼 《地质论评》1992,38(2):184-189
本文研究的是笔者等在冀西北长城系串岭沟组宣龙式铁矿层中发现的微体植物化石,这些化石都保存在铁质叠层石(肾状赤铁矿)和铁质核形石(鲕状赤铁矿)的基本层中。微化石以丝状体为主,部分为球状体。归属于原核生物蓝藻门颤藻科的两个属和色球藻科的一个属。化石层同位素年龄约在1800—1757Ma。这些化石与北美冈弗林特组微化石比较,既有些相似,又有些区别。该化石的发现为研究铁矿的成因,指示沉积环境及层位对比都很有意义。  相似文献   
175.
矿物标型六性及其在胶东金矿中的应用   总被引:2,自引:0,他引:2  
目前矿物标型研究和应用已进入一个新的阶段。作者从哲学的高度,把国内外矿物标型特征的分散研究加以集中概括和总结,提出了“矿物标型六性”的普遍规律,即普遍性、特殊性、变化性、相应性、继承性和分带性,对矿物标型特征研究具重要的指导意义。这些规律在胶东金矿中得到广泛应用,并已取得良好效果。  相似文献   
176.
凤凰山铜(金)矿床产于燕山晚期花岗闪长岩及石英二长闪长斑岩与三叠系碳酸盐岩的接触带,先后包括矽卡岩型和斑岩型两期矿化,并可细分为9个成矿阶段。矿石中广泛出现角砾状和细脉状、网脉状构造。流体包裹体特征及显微冷热台测温资料表明,成矿流体存在过沸腾和局部超高压等现象。两个成矿期都经历了从高温高盐度向低温低盐度的转变,成矿溶液的主要成分也由钾钠型变成了钠钙型。来源于岩浆热液的早期含矿流体与来自围岩的地下水热液的混合可以解释成矿流体的这种演化。  相似文献   
177.
Catalytic ozonation has attracted much attention in treatment of wastewater for its mild conditions. Phenol and its ramifications are common components in a wide variety of wastewaters including those from coal conversion processes, coking plants, petroleum refineries and several chemical industries. In this paper, natural brucite and magnesia have been successfully used in catalytic ozonation of phenol. And the mechanisms of catalysis were also investigated. From Figs. 1 and 2, it can be found that both brucite and magnesia have remarkable catalysis on degradation of phenol and removal of Chemical Oxygen Demand (COD). The pH of solutions on the process of ozonation alone, catalytic ozonation with brucites and with magnesia were 6.35-2.76, 10.18-8.52 and 10.58-10.83, respectively. It can be concluded that alkali environment plays a critical role for catalytic ozonation of phenol. We also found that the alkaline minerals reacted on the surface with oxalic acid and other low molecular-weight acids which are intermediate products in ozonation, but those intermediate products could be mineralized into carbon dioxide completely with enough ozonation time.  相似文献   
178.
In southern Rocky Mountains, catchments characterized by acidic, metalliferous waters that are relatively unaffected by human activity usually occur within areas that have active or historical mining activity. The US Geological Survey has utilized these mineralized but unmined catchments to constrain geochemical processes that control the surface- and ground-water chemistry associated with near surface acid weathering as well as to estimate premining conditions. Study areas include the upper Animas River watershed, Lake City, Mt. Emmons, and Montezuma in Colorado and Questa in New Mexico. Although host-rock lithologies range from Precambrian gneisses to Cretaceous sedimentary units to Tertiary volcanic complexes, mineralization is Tertiary in age and associated with intermediate to felsic composition, porphyritic plutons. Pyrite is ubiquitous. Variability of metal concentrations in water is caused by two main factors: mineralogy and hydrology. Parameters that potentially affect water chemistry include: host-rock lithology, intensity of hydrothermal alteration, sulfide mineralogy and chemistry, gangue mineralogy, length of flow path, precipitation, evaporation, and redox conditions. Springs and headwater streams have pH values as low as 2.5, sulfate up to 3700 mg/L and high dissolved metal concentrations (for example: Al up to 170 mg/L; Fe up to 250 mg/L; Cu up to 3.5 mg/L and Zn up to 14 mg/L). With the exception of evaporative waters, the lowest pH values and highest Fe and Al concentrations occur in water draining the most intense hydrothermally altered areas consisting of the mineral assemblage quartz-sericite-pyrite. Stream beds tend to be coated with iron floc, and some reaches are underlain by ferricrete. When iron-rich ground water interacts with oxygenated waters in the stream or hyporheic zone, ferrous iron is oxidized to ferric iron, which is less soluble, leading to the precipitation of iron oxyhydroxides.  相似文献   
179.
The Bonnifield district hosts 26 tmmined volcanogenic massive sulfide (VMS) occurrences. Environmental geochemical samples of water and stream sediment were collected at several occurrences, concentrating on the two best-exposed and largest deposits, Red Mountain (RM) and Sheep Creek (SC). Limited samples were also collected at the poorly exposed WTF deposit. The deposits are Late Devonian to Early Mississippian, and are hosted by felsic metavolcanic and carbonaceous schist members of the Totatlanika Schist or Keevy Peak Fm. Spring and stream waters at RM and SC have pH values commonly 〈3.5 (as low as 2.4 at RM and 2.5 at SC), high conductivity (up to 11000 μS/cm), and very high (Is to 100s mg/L) dissolved contents of Al, Cd, Co, Cu, Fe, Ni, and Pb. Waters at RM are characterized by extremely high REE contents (summed REE median 3200 μg/L, n=33). At both RM and SC, pyrite oxidation and dissolution produce low pH waters that interact with and dissolve bedrock minerals, resulting in acidic, metal-laden, naturally degraded streams that are mostly devoid of aquatic life. Ferricrete is common. In contrast, WTF barely produces a surficial environmental footprint, mostly due to topography and relief. RM and SC are well exposed in the areas of relatively high relief, and both exhibit extensive areas of quartz-sericite-pyrite-alteration. While WTF shares many of the same deposit-and alteration characteristics, it is concealed by tundra in a large, nearly flat area. Surface water at WTF is absent and outcrops are sparse. Even though WTF is roughly the same size as Red Mountain (both around 3 million tonnes) and has similar base- and precious-metal grades, the surficial geochemical manifestation of WTF is minimal. However, exposure through mining of the altered, mineralized rock at WTF potentially could initiate the same processes of pyrite oxidation, acid generation, and mineral dissolution that are observed naturally at RM and SC.  相似文献   
180.
Although hydrotalcite, or layered double hydroxides (LDHs), is not a common mineral, it is an important material that can be easily synthesized in laboratory. In this study, structural evolvement and BET surface area changes of heat treated Mg/AI-LDH is evaluated by XRD, TEM and N2-BET analyses. The results indicate that the magnesium-aluminum LDH with carbonate as interlayer anion, periclase-like oxides was formed at temperatures of 400-800℃. Meanwhile, 2-3 nanometer mesoporous were formed during decomposition of LDH. However, the heat treated samples still preserve the morphology of the original LDH plates. Periclase-like formed from LDH heat treatment may re-hydrolyze and recover the structure of LDH. However, crystallinity of the recovered LDH is lower than that of the original LDH. This heat treatment will result in formation of (Mg, Al)-oxide nano-crystals and nanopores among the nano-crystals. When heating temperature exceeds 1000, the periclase-like (Mg, Al)-oxide is transformed into a composite with periclase (MgO) and spinel phases. The periclase can be re-hydrolyzed and dissolved in HCl solution. After acid treatment, the sample with a high surface area is composed of spinel nano-crystals and nanopores among them. Our results will provide a new and economic way to synthesize mesoporous materials through pathways of phase transformation of precursor materials with different composition.  相似文献   
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