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51.
Fe‐rich metapelitic granulites of the Musgrave Block, central Australia, contain several symplectic and coronal reaction textures that post‐date a peak S2 metamorphic assemblage involving garnet, sillimanite, spinel, ilmenite, K‐feldspar and quartz. The earliest reaction textures involve spinel‐ and quartz‐bearing symplectites that enclose garnet and to a lesser extent sillimanite. The symplectic spinel and quartz are in places separated by later garnet and/or sillimanite coronas. The metamorphic effects of a later, D3, event are restricted to zones of moderate to high strain where a metamorphic assemblage of garnet, sillimanite, K‐feldspar, magnetite, ilmenite, quartz and biotite is preserved. Quantitative mineral equilibria calculations in the system K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 (KFMASHTO) using Thermocalc 3.0 and the accompanying internally consistent dataset provide important constraints on the influence of TiO2 and Fe2O3 on biotite‐bearing and spinel‐bearing equilibria, respectively. Biotite‐bearing equilibria are shifted to higher temperatures and spinel‐bearing equilibria to higher pressures and lower temperatures in comparison to the equivalent equilibria in K2O–FeO–MgO–Al2O3–SiO2–H2O (KFMASH). The sequence of reaction textures involving spinel is consistent with a D2 P–T path that involved a small amount of decompression followed predominantly by cooling within a single mineral assemblage stability field. Thus, the reaction textures reflect changes in modal proportions within an equilibrium assemblage rather than the crossing of a univariant reaction. The D3 metamorphic assemblage is consistent with lower temperatures than those inferred for D2. 相似文献
52.
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)5 S15 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 Zn10 Fe3 Cu2 S15. 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
The ideal chemical formula of the solid solution series can well be presented as Zn
53.
54.
低聚合羟基铁离子-蒙脱石复合体吸附砷的实验研究 总被引:15,自引:2,他引:15
将提纯的钙蒙脱石与羟基铁离子溶液作用,制备了低聚合羟基铁-蒙脱石复合体,用化学分析,电子探针分析,粉晶X射线衍射分析,差热分析和穆斯堡尔谱分析等手段。对蒙脱石原样,低聚合羟基铁-蒙脱石复合体和相同条件下制备的铁的含水氧化物进行了表征。在实际土壤的酸度(pH=4-7)和温度(18-40℃)条件下,进行了低聚合羟基铁-蒙脱石复合体吸附有害元素砷的实验,探讨了复合体的砷吸附能力与pH值,温度,吸附时间,砷初始浓度,离子强度间的关系,并与蒙脱石和铁的含水氧化物的砷吸附行为进行了对比,研究表明,在实验条件下,低聚合羟基铁-蒙脱石复合体对砷具有明显的亲合力,低聚合羟基铁-蒙脱石复合体吸附砷的过程有可能是地表岩石和土壤中重要的地球化学过程,是影响砷地地表,特别是土壤中迁移,富集的重要因素。 相似文献
55.
X射线荧光光谱法测定叶腊石中的铝铁钾钠 总被引:1,自引:0,他引:1
采用同一矿区已知成分含量的叶腊石配制标样系列,克服了粉末法测定叶腊石中Al2O3,Fe2O3,K2O,Na2O的矿物和粒度效应。分析结果准确度满足出口材料的检测要求。 相似文献
56.
HanBin Xue René Gächter Laura Sigg 《Aquatic Sciences - Research Across Boundaries》1997,59(2):176-189
Data on the cycling of Cu and Zn in two eutrophic lakes are presented: Lake Greifen that becomes seasonally anoxic in its
hypolimnion and Lake Sempach that is aerated during winter and oxygenated during summer. They suggest that hypolimnetic oxygenation
1) enhances the release of copper from the sediment but 2) also accelerates the entrapment and deposition of Cu and Zn by
freshly formed Mn- and Fe-oxides. 相似文献
57.
中条山—塔儿山成矿带属滨西太平洋成矿域华北断块金、银、铜、铅、锌、锰、铝土矿、金刚石成矿区中的3级成矿带,其中包括2个成矿系列、7个成矿亚系列和11个矿床式。2个成矿系列具有成矿世代的“双层性”、成矿物质来源的二元性、成矿作用的三阶段和矿化带展布与地质构造单元的趋近性等一系列特征 相似文献
58.
59.
The spinel solid solution was found to exist in the whole range between Fe3O4 and γ-Fe2SiO4 at over 10 GPa. The resistivity of Fe3−
x
Si
x
O4 (0.0<x<0.288) was measured in the temperature range of 80∼300 K by the AC impedance method. Electron hopping between Fe3+ and Fe2+ in the octahedral site of iron-rich phases gives a large electric conductivity at room temperature. The activation energy
of the electron hopping becomes larger with increasing γ-Fe2SiO4 component. A nonlinear change in electric conductivity is not simply caused by the statistical probability of Fe3+–Fe2+ electron hopping with increasing the total Si content. This is probably because a large number of Si4+ ions occupies the octahedral site and the adjacent Fe2+ keeping the local electric neutrality around Si4+ makes a cluster, which generates a local deformation by Si substitution.
The temperature dependence of the conductivity of solid solutions indicates the Verwey transition temperature, which decreases
from 124(±2) K at x=0 (Fe3O4) to 102(±5) K at x=0.288, and the electric conductivity gap at the transition temperature decreases with Si4+ substitution.
Received: 15 March 2000 / Accepted: 4 September 2000 相似文献
60.
富钴结壳生长过程中铁锰氧化物矿物组合的变化 总被引:3,自引:0,他引:3
富钴结壳的矿物学研究是一个难点,本文运用电子探针微区分析结合X射线衍射和矿相显微镜观察的综合方法对富钴结壳中的铁锰氧化物矿物组合及其组分变化进行了研究,研究发现,富钴结壳是从与胶状粘土类混合共沉积开始生长的,结壳内部的韵律层和柱状构造也是始于粘土层终于粘土层的;铁锰团粒的核心一般是较纯的水羟凶国矿小核心,可能是在生物媒介作用下在水体中形成后沉降叠积的,FM、FPE海山结壳的中层存在一较纯水羟锰矿层,但该层中Co含量FM15比FPE06低得多,可能反映了FM15在该层形成时Co通量较低,而该层在FN12中不存在,反映了区域环境的较大差异,在FN12火焰状构造亚带存在Mn氧化物和Fe氧化物的极度分异现象,可能反映了结壳形成环境的重大变化。 相似文献