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1.
Hydrothermal vein minerals directly associated with native gold mineralization in the Muruntau vein system (Uzbekistan) have been studied for noble gas, carbon isotope and halogen chemistry of the trapped ore-related fluids. Helium trapped in early arsenopyrite 1, which has preserved the original fluid signature better than associated scheelite and quartz, indicates a small input from a mantle source (?5% of total He). However, the overwhelming majority of the He in the fluid (∼95%) is from crustal sources. The noble gases Ne, Kr and Xe in the sample fluids are dominated by gases of atmospheric origin. The carbon isotope (δ13C: −2.1‰ to −5.3‰) and halogen characteristics of the fluids (log Br/Cl: −2.64 to −3.23) lend further support for the activity of juvenile fluids during the main ore stage. The high proportion of crustal components in the ore-forming fluids may be explained by intense fluid-rock interaction and is also supported by previous Nd and Sr isotope studies. The involvement of a juvenile fluid component during the main stage of hydrothermal activity at Muruntau (∼275 Ma) can be linked to the emplacement of lamprophyric dikes at Muruntau, due to apparently overlapping ages for high-temperature alteration, related ore vein formation and intrusion of the dikes. The input of mantle-derived fluids, possibly related to the Hercynian collisional event in the western Tien Shan, stimulated intense fluid-rock interaction in the crust. In this context, the mantle-derived fluid should be considered as one possible carrier of metals. Significant amounts of external meteoric fluids circulating in fracture systems are interpreted to have modified the noble gas signature of fluid in quartz, mostly during late, low temperature fluid circulation.  相似文献   
2.
This short note reviews our thinking on how IGGOS can best achieve a high status within the set of global monitoring programmes. If such a high status can be obtained, then the importance of geodetic networks and services will be recognized more widely, and their activities will consequently be better resourced in the long term. One particular aspect concerns how IGGOS can complement the roles of the various IGOS partners within global monitoring. The different ways in which IGGOS can contribute to IGOS are outlined.  相似文献   
3.
Kyanite eclogites occur as part of the Münchberger nappe pile in NE-Bavaria, West Germany. Eclogites are overprinted by subsequent amphibolite facies metamorphism. The preservation of primary eclogitic textures as well as symplectitic textures are indicative of rapid decompression. Eclogite formation is estimated to have occurred under conditions of high H2O-activities at pressures between 20 and 26 kbar and temperatures ranging between 590 and 660° C, as is shown by the coexistence of omphacite (Jd 50), kyanite, zoisite and quartz. Minimum pressure estimates, independent of the water activity, range between 9 and 16 kbar at the relevant temperatures. Detailed studies of fluid inclusion reveal two predominant groups of aqueous-brine inclusions: high salinity (14–17 wt% NaCl equiv.) and low salinity (0–8 wt% NaCl equiv.) inclusions. Fluid compositions of both groups of inclusions yield isochores passing close to the estimated amphibolite facies PT-field. The compositions of these fluids are in good agreement with fluid compositions considered from mineral equilibria. None of the fluid inclusions has densities appropriate for eclogite facies metamorphism, but probably reflect later amphibolite facies metamorphism.  相似文献   
4.
Drillcores and waters from Wairakei and Broadlands geothermal areas New Zealand have been analyzed for Li, Rb, Cs, Na, K, Mg, Ca, Al, Ti, Mn, and Be. The drillcores were altered to various degrees at temperatures below 300°C in slightly alkaline chloride water, probably derived from rock-water interaction in untapped horizons at higher temperature. It changes its composition as it leaches Ca and Na from the rock and adds K, Rb, Cs and Li. Evaluation of these changes in relation to the dimensions of the altered zone under observation suggests that a high mass ratio of water to rock (e.g., 100) and a period of up to 1 million years are responsible for the present stage of alteration.Increase of K and Rb in the altered rocks is a result of the formation of abundant adularia in addition to illite. The KRb ratio of the rock decreases during alteration but remains higher than that of the fluid. Only clay materials and zeolites that preferentially absorb Rb give slightly lower KRb ratios than the fluid.The mineral phases responsible for the uptake of lithium during alteration are chlorite (300 ppm Li) and quartz (up to 430 ppm Li). Li uptake in quartz is considered to be the mechanism by which Al-rich quartz crystallises from alumino-silicates. LiAl atomic ratios of 0.3–0.57 and Al concentrations up to 3000 ppm have been observed.Relatively small concentrations of Cs are found in potassic minerals (e.g. 10 ppm Cs in adularia, 44 ppm Cs in illite). However, 240 ppm Cs are found in wairakite from Wairakei equilibrated at 235°C. Lower equilibration temperatures may lead to higher cesium concentrations. This effect, in conjunction with a more concentrated hydrothermal fluid, could explain a content of 4500 ppm Cs in wairakite extracted from a drillcore taken in the El-Tatio geothermal field in Chile.  相似文献   
5.
The amount of energy used in tectonic processes is computed, and estimated as 2.108 kw. It is shown that thermal contraction can yield only much smaller amounts of energy, and must be discarded. Tectonic energy is believed to come, either from convection currents in the mantle, either from gravitational differentiation, or both.  相似文献   
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7.
苏文  高俊  Reiner  KLEMD  熊贤明 《岩石学报》2006,22(5):1380-1386
运用电子探针和显微Fourier变换红外光谱技术,对新疆西天山3个榴辉岩样品中的石榴石进行了详细的主量元素和结构水分析。结果显示,石榴石发育以核部富锰铝榴石组分、边部富镁铝榴石组分进变质作用的成分环带。石榴石中OH^-1分布也具有规律:核部→边缘。其结构水OH^-1逐步增加,即从核部的89-239ppm增加到边部的367-658ppm;与石榴石边部相比,石榴石的核部含有较低的OH^-1,却含有较高的H2O和Mn含量。这表明,在蓝片岩向榴辉岩进变质作用过程中,含水矿物脱水反应而释放出大量的分子水,这部分水促进了高压变质反应,形成榴辉岩相矿物,石榴石核部的结晶就是在富水和Mn的条件下进行的。随着高压变质作用的继续,石榴石核部的分子水逐步失水而进入石榴石晶格,形成结构水。因此,在高压变质作用过程中,OH^-1演化实际上是一个由内部不平衡逐步向平衡转变过程。P588.348  相似文献   
8.
The formal stereological transformation equation for particle sieve size distribution from measurements in lower dimensional spaces is applied to laser diffractometer measurements. The transformation function for iron ore particles is measured experimentally, and modeled. The solution is tested against the measured transformation function data as well as synthetic composite distributions of the original sample. The natural size distribution of a sample taken from a grinding circuit stream was measured by a combination of standard sieving and cyclosizer, and the result is compared to the transformed size distribution calculated from laser diffractometer measurements. The stereological transformation technique performed well in all cases.  相似文献   
9.
Hawaiian volcanoes characteristically have but few of the many types of minerals found in incrustations of other volcanic areas. In Hawaii sulfates resulting from air oxidation of volatiles predominate, and fluorides produced during rock alteration by fumarolic gases are prominent. Halides are generally found where reducing conditions exist in fumaroles and lava lake drill holes. The most common mineral types are sulfur, opaline silica, gypsum, ralstonite, and thenardite. Minerals from the same deposit are found to vary markedly in the content of the less abundant components. Condensates from vapor issuing from fumaroles show little quantitative relationship in component content to incrustations deposited at the same fumaroles. It is believed that an energetically favorable isomorphic substitution of some elements in the crystal lattice of a depositing mineral may lead to the build-up of a high concentration of an element from a lean vapor. Equilibrium calculations applied to condensate studies give a good quantitative approximation to the concentrations of the elements found in natural systems, but when applied to incrustations they serve only to indicate general compositional relations. Laboratory studies have shown the important role of chlorides in metal transfer in the gas phase in high-temperature aqueous systems, but only in the absence of oxygen. These studies also demonstrated the important role of HF in rock alteration and in the transfer of silica.  相似文献   
10.
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