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61.
Organic matter has been observed in cores of the Soultz-sous-Forêts granite (Alsace, France) at depths between 2158 and 2160 m, in a highly fractured and altered zone. The granite is overlain by a 1400-m-thick sedimentary cover containing petroleum (Pechelbronn oil field). The Soultz area is devoted to Hot Dry Rock geothermics thanks to a high geothermal gradient (up to 100 °C/km). During drilling operations, an artesian source produced oil in a fractured zone of the sedimentary cover (Buntsandstein). Its gas-chromatography and mass-spectrometry (GC-MS) analysis revealed the presence of normal alkanes (n-alkanes, i.e. linear hydrocarbons) centered on C17, branched alkanes with a major C19 peak, and few unsaturated hydrocarbons. The aromatic fraction is present in small amounts. In the Soultz granite, where it is altered, organic matter is exclusively associated with tosudite (interstratified clay mineral) which crystallized in plagioclase sites during a hydrothermal alteration episode. Organic matter has been later displaced and concentrated along veinlets in which illite and carbonates have crystallized during another hydrothermal alteration stage. The soluble organic matter analyzed by GC-MS is composed of aliphatic acids, n-alkanes with a bimodal C18 and C24-C25 centered distribution, alkylbenzenes and aromatic acids. Organic compounds in the granite would either originate from a single source (immature sediments) or from two sources (immature sediments and migration of the Pechelbronn oil). No real evidence was found to prove which hypothesis is the best one. The presence of organic matter in the granite shows the importance of fluid flows between the sedimentary cover and the granitic basement through major fractures. In addition, the impregnation of plagioclase pseudomorphs with organic matter is made possible due to their high interconnection degree and to the intergranular microfracturation of the granite. The succession of several hydrothermal events with different physico-chemical characteris- tics may also be inferred from the occurrence of organic matter found in association with neoformed clay minerals in the granite.  相似文献   
62.
Resistivity prospecting is the main tool used to investigate the shallow structure of the ground. A series of new techniques for determining the 2-D and 3-D geometry of the ground is now finding increasing use, but the light and simple Wenner prospecting technique remains a practical and efficient tool for rapidly mapping lateral variations in resistivity. When the resistivity changes are smooth, 1-D modelling can be used to interpret the data, and the criteria governing this approximation can be defined from synthetic data generated by a 3-D slab-model. For a Wenner array, two quadripole configurations can be used, Normal and Dipole-Dipole. For these two configurations the width of the transition zone, the apparent anisotropy effect and the precision of the resistivity values recovered from 1-D inversion differ. However the simultaneous inversion of both sets of data gives better results than for either configuration by itself. Two examples illustrate that in geological contexts where the thickness of the weathered zone causes the changes in the apparent resistivity value, this parameter can be recovered from 1-D inversion.  相似文献   
63.
Detailed petrographic and mineralogic investigations of an albite-lepidolite granite at Echassières (Massif Central, France; scientific deep drill program) shows the existence of hydrothermal stages which are closely related to the magmatic and structural history. According to fluid inclusion data, K-Ar datations and 18O/16O-D/H compositions of secondary minerals, two successive hydrothermal periods have been recognized. The early one (273–268 million years) produced a series of aluminous phyllosilicates: muscovite, pyrophyllite, donbassite, tosudite, kaolinite which are observed as vein deposits (<10 mm wide) and alteration products of primary minerals in wall-rocks. The vein system was sealed by monomineralic assemblages during a cooling period (400–150°C). This early hydrothermal alteration stage was controlled by interactions of rock with low salinity (1–10 wt% NaCl equivalent) fluids expelled from the granitic body during the cooling processes. The chemical properties of these fluids were the following: low pH, very low Mg and Fe and high Li, Na and K contents. Thermodynamic calculations show that the sequence pyrophyllite, Li-bearing donbassite, tosudite is mostly temperature dependent. From the chemical composition of secondary minerals and isotopic data it can be deduced that these fluids, which have a meteoric origin, have been expelled from the granite body during its cooling period and after interaction with it at high temperature. The late hydrothermal stage corresponds to deposits of fluorite and Fe-Mg rich illite (151 million years) in subvertical fractures. Temperature conditions did not exceed 250° C and fluids came through the surrounding metamorphic rocks into the granitic body. IIlite/smectite mixed-layer minerals have been identified in subvertical fractures which were opened during Tertiary periods. In the host micaschists, successive hydrothermal alterations took place during the cooling of the Beauvoir granite. Early magmatic fluids interacted with these micaschists. Locally, the metamorphic assemblage is replaced by a metasomatic one. Secondary topaz and (F, Li)-rich mica crystals were formed over a range of 450 of 150°C. Later hydrothermal fluids reacted with the country rocks to form phengite-biotite, chlorite-illite and kaolinite over a range of 300 to 150°C. Illite/smectite mixed-layer minerals crystallized in the roof micaschists and within the Beauvoir granite during the Tertiary alteration period. Meteoric water invaded open fractures producing supergene alteration mineral assemblages.  相似文献   
64.
The concentrations of major and trace elements have been determined in igneous rocks from Apollo 15. All materials analyzed have typical depletions of Eu except for minerals separated from sample 15085. Four samples have concentrations of trace elements that are similar to those of KREEP. The samples of mare basalt from Apollo 15 have higher concentrations of FeO, MgO, Mn, and Cr and lower concentrations of CaO, Na2O, K2O, and rare-earth elements (REE) as compared to the samples of mare basalt from Apollos 11, 12, and 14. The samples can be divided into two groups on the basis of their normative compositions. One group is quartz normative and has low concentrations of FeO while the other is olivine normative and has high concentrations of FeO. The trace element data indicate that the samples of olivine normative basalt could be from different portions of a single lava flow. At least two and possible three parent magmas can be identified from the samples of the quartz normative group on the basis of their concentration ratios of Sm to Eu. Within each group, the compositions of the samples appear to be related by crystallization of olivine or pyroxene. Significant variations of the ratio of concentration of Sm to Eu cannot be produced without plagioclase-liquid equilibrium. The source material of mare basalt may be depleted in Eu. Alternatively, the magmas may have assimilated a small volume of material similar to KREEP.Paper dedicated to Prof. Harold C. Urey on the occasion of his 80th birthday on 29 April 1973.  相似文献   
65.
Following the spill of fuel oils from the New Carissa in February 1999, approximately 300 km of beaches on the Pacific coast of North America were surveyed. A long-term observation program focused on the documentation of stranded tar balls in the vicinity of the spill site. Systematic beach surveys which were conducted over the period March 1999 to April 2001 and semi-logarithmic scale, time-series plots proved the most useful format for identifying trends. Beach monitoring continued through to August 2001. by which time 212 tar balls had been analyzed by GC/MS for their chemical characteristics. The samples of tar balls collected between February 1999 and August 2001 were qualitatively compared with New Carissa source oils (NCSO) and 101 (48%) were not consistent with NSCO. The presence of tar balls that are not related to an incident can confound attempts to define cleanup or endpoint criteria and to assess possible injury to natural resources.  相似文献   
66.
The Callovo-Oxfordian claystones located at 500 m depth at Bure (Meuse, France) are currently being investigated by Andra (the French National Radioactive Waste Management Agency) for testing the feasibility of long-term and deep geological nuclear waste disposal. In order to evaluate its potential as a geological barrier, it is very important to study, assess and describe its physico-chemical variability. The molecular biomarker composition of 150 samples of these claystones and their surrounding limestones carry diverse information on the sources of the sedimentary organic matter, the chemistry of the depositional environment, the preservation and diagenesis conditions. It also allows assessing the degree of lateral and vertical variability of the organic matter within these sedimentary series. The abundance of unsaturated biomarkers, the distribution of steroids and hopanoids and CPI values >2 prove the thermal immaturity of the organic matter. The co-occurrence of plankton, bacteria and land plant biomarkers indicate that the organic matter is a mixture of marine and continental contributions. The data also reveal that the organic matter was deposited under oxic and open-sea conditions except for a brief event of photic zone anoxia at the beginning of the Middle Callovian. In the claystones, the geosynthesis of diasterenes is favored to the detriment of the formation of steranes, especially in smectite-rich levels, and the organic matter is rapidly isolated from oxidizing then reducing conditions after the deposition due to the protective effect of clays. On the scale investigated, the claystones are characterized by a unique molecular facies and are thus homogenous from their organic content point of view. Yet, detailed investigation of specific molecular families indicates changes related to major claystone–limestone transitions. The homogeneity of these claystones can be explained by the paleogeographic position of their depositional setting and the plane and sub-horizontal paleotopography on which they were deposited. This study demonstrates the efficiency of organic geochemistry in the assessment of the variability of geological barriers.  相似文献   
67.
The Balkuyumcu region, located in the southwestern part of Ankara in the Izmir-Ankara suture zone (central Anatolia, Turkey), consists of basic andesitic, andesitic, dacitic and rhyolitic rocks extruded during the Early Miocene (20–22 Ma) as a result of post-collisional volcanism. Balkuyumcu volcanic rocks can be divided into two groups on the basis of their mineralogy and composition: The basic andesitic (BA) and andesitic, dacitic and rhyolitic (ADR) groups. The ADR and BA group of rocks have adakite-like and calc-alkaline characteristics, respectively. The ADR group has higher SiO2 content, Sr/Y and La/Yb ratios and low MgO, Mg#, Y and Yb contents than the BA group. Both groups have nearly the same Sr, Nd isotopic compositions and display similar normalized multi-element patterns with enrichments in LILE and LREE, depletions in Nb, Ti, Zr, P and a lack of Eu anomalies. Major, trace element and Sr, Nd isotopic data indicate that both groups of rocks were derived from the same source but affected by different magmatic processes during ascent. The adakite-like rocks may have been produced by partial melting of thickened lower continental crust. Fractional crystallization also played a major role in their formation. However, the BA group rocks were derived from partial melting of lower continental crust that was probably delaminated. These rocks appear to have had limited interaction with mantle peridodite during ascent to the surface.  相似文献   
68.
Neogene volcanism in the Eastern Rif (Morocco) comprises a series of calc-alkaline, potassic calc-alkaline, shoshonitic and alkaline volcanic rocks. According to new stratigraphical, along with new and previous chronological and geochemical data, the orogenic volcanism was successively (1) calc-alkaline (basaltic andesites and andesites: 13.1 to 12.5 Ma, rhyolites: 9.8 Ma), (2) K-calc-alkaline (basaltic andesitic to rhyolitic lavas and granodiorites: 9.0 to 6.6 Ma), and (3) shoshonitic (absarokites, shoshonites, latites, trachytes: 7.0 to 5.4 Ma). The later Pliocene volcanism was basaltic and alkaline (5.6 to 1.5 Ma). The calc-alkaline and K-calc-alkaline series exhibit lower K2O (0.7–5.3 wt.%), Nb (8–19 ppm) contents and higher 87Sr/86Sr (0.70773–0.71016) than the shoshonitic series (K2O: 2.4–7.2 wt.%, Nb: 21–38 ppm, 87Sr/86Sr: 0.70404–0.70778). Pliocene alkaline basalts have a sodic tendency (Na2O/K2O: 1.7–3.5), high Nb content (up to 52 ppm), and low 87Sr/86Sr ratio (0.70360–0.70413). The variations through time of K2O, Nb and Sr isotopic ratio reflect different mantle sources: (i) calc-alkaline, potassic calc-alkaline and shoshonitic series are derived from a mantle source modified by older subduction, (ii) alkaline basalts are derived mainly from an enriched mantle source. Through time, incompatible elements such as Nb increased while 87Sr/86Sr decreased, suggesting a decreasing influence of metasomatized mantle (inherited subduction). Such evolution is related to the post-collision regimes operating in this area, and could be linked to the succession of extensional, compressional and strike-slip fault tectonics.  相似文献   
69.
Erciyes stratovolcano, culminating at 3917 m, is located in the Cappadocian region of central Anatolia. During its evolution, this Quaternary volcano produced pyroclastic deposits and lava flows. The great majority of these products are calc-alkaline in character and they constitute Kocdag and Erciyes sequences by repeated activities. Alkaline activity is mainly observed in the first stages of Kocdag and approximately first-middle stages of Erciyes sequences. Generally, Kocdag and Erciyes stages terminate by pyroclastic activities. The composition of lavas ranges from basalt to rhyolite (48.4–70.5 wt.% SiO2). Calc-alkaline rocks are represented mostly by andesites and dacites. Some compositional differences between alkaline basaltic, basaltic and andesitic rocks were found; while the composition of dacites remain unchanged. All these volcanics are generally enriched in LIL and HFS elements relative to the orogenic values except Rb, Ba, Nb depleted alkaline basalt. 87Sr/86Sr and 143Nd/144Nd isotopic composition of the volcanics range between 0.703344–0.703964, 0.512920–0.512780 for alkaline basalts and change between 0.704322–0.705088, 0.512731–0.512630 for alkaline basaltic rocks whereas calc-alkaline rocks have relatively high Sr and Nd isotopic ratios (0.703434–0.705468, 0.512942–0.512600). Low Rb, Ba, Nb content with high Zr/Nb, low Ba/Nb, La/Yb ratio and low Sr isotopic composition suggest an depleted source component, while high Ba, Rb, Nb content with high La/Yb, Ba/Nb, low Zr/Nb and low 87Sr/86Sr ratios indicate an OIB-like mantle source for the generation of Erciyes alkaline magma. These elemental and ratio variations also indicate that the different mantle sources have undergone different degree of partial melting episodes. The depletion in Ba, Rb, Nb content may be explained by the removal of these elements from the source by slab-derived fluids which were released from pre-collisional subduction, modified the asthenospheric mantle. The chemically different mantle sources interacted with crustal materials to produce calc-alkaline magma. The Ba/Nb increase of calc-alkaline samples indicates the increasing input of crustal components to Erciyes volcanics. Sr and Nd isotopic compositions and elevated LIL and HFS element content imply that calc-alkaline magma may be derived from mixing of an OIB-like mantle melts with a subduction-modified asthenospheric mantle and involvement of crustal materials in intraplate environments.  相似文献   
70.
We present analyses of spheres magnetically extracted from mid-Pacific abyssal clays 0–500,000 years old. The concentration of spheres >200 μm is a few times 10 ppb. The spheres were divided into three groups using their dominant mineralogy, and are named iron, glassy, and silicate. Most spheres were formed from particles that completely melted as they separated from their parent meteoroids during the ablation process. However, some of the silicate spheres contain relict grains of the parent meteoroids that did not experience any melting. Typically, these relict grains are olivine crystals whose cores are Mg-rich (Fo89–99). Commonly the outer rims of these grains were altered during heating. Other relict mineral grains include enstatite, ferrous spinel, chromite, and pentlandite.The three groups of spheres may possibly indicate some genetic significance. It seems reasonable to expect iron-rich spheres to be produced during ablation of iron and metal-rich silicate meteoroids. Metal spheres are probably not produced by ablation of predominantly silicate meteoroids because studies of fusion crusts and laboratory ablated silicate materials have never yielded separate metal spheres, but rather have produced spheres with intergrown iron oxide and silicate phases. The iron spheres possess identical mineralogy with the fusion crusts of Boguslavka, Norfork, and N'Kandhla iron meteorites as well as with the ablation debris created in the laboratory using iron and nickel-iron samples.The glassy spheres are considerably more Fe-rich than the silicate spheres. They consist of magnetite and a Fe-rich glass which is relatively low in Si. Some of these spheres may have experienced pronounced volatile depletion during the ablation process and could have been derived from silicate or metal-rich silicate meteoroids.The silicate spheres are undoubtedly derived from ablation of stony meteoroids. Two of the mineral assemblages occurring in these spheres (olivine-magnetite-glass and sulfide) are identical to those described in the natural fusion crusts of Allende, Orgueil, and Murchison meteorites, laboratory-made ablation debris, and melted interplanetary dust collected from the stratosphere. Bulk compositions and relict grains are useful for determining the parent meteoroid types for the silicate spheres. Bulk analyses of spheres have non-volatile elemental abundances similar to chondritic abundances. Analyses of relict grains identified high-temperature minerals which often occur as larger crystals in a fine-grained matrix that is characterized by voids. These voids were caused by escaping volatiles as minerals decomposed during ablation. Because larger crystals of higher-temperature minerals are associated with fine-grained, low-temperature, volatile-rich matrix, the obvious candidates for parent meteoroids of the silicate spheres containing relict grains are carbonaceous chondrites.  相似文献   
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