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11.
By means of a new homogeneous set of data from 34 double-lined detached systems, we have recalibrated the colour-surface brightness correlation in the interval –0.3(B-V)o0.95. A comparison is made with Wesselink's calibration. We find that Wesselink's method can provide a good estimate of the stellar radii.  相似文献   
12.
The Villeta Group of Colombia and equivalent stratigraphic units of Venezuela and Ecuador comprise marine sequences ranging from Albian to Santonian in age. Deposition of the Villeta Group was presumed to take place entirely in quiet tectonic conditions in a passive margin setting that occupied NW South America. From a large database of 2D/3D seismic, well, surface geology, and biostratigraphic data, we present evidence for intra-Villeta (mostly late Albian–Cenomanian) deformation in parts of the Upper Magdalena Valley and Eastern Cordillera of Colombia, controlled by transpressional fault reactivation, produced by transpressional fault reactivation and thrusting that resulted in an angular unconformity. This event has been largely unnoticed in the literature, but previously scattered evidence supports our observations, suggesting regionally extensive tectonism. Published fission-track age determinations and other geologic evidence from Colombia and Venezuela suggest significant uplifts around 80–100 m.y., which may reflect changes in the subduction regime, with compressional deformation in certain regions and extensional deformation in others. A late Albian onset of compressional deformation along the Colombian and Peruvian segments of the Andes may be related to the opening of the South Atlantic Ocean at equatorial latitudes. Identification of tectonic activity with development of an unconformity in intra-Villeta times provides new insights into understanding the evolution of the Upper Magdalena Valley and adjacent areas of Colombia and western Venezuela and creates new possibilities for hydrocarbon exploration, with additional trapping phases, better reservoir preservation by early migration and secondary porosity, and ultimately facies changes with stratigraphic potential.  相似文献   
13.
Manganese oxides form typically in natural aqueous environments via Mn(II) oxidation catalyzed by microorganisms, primarily bacteria, but little is known about the structure of the incipient solid-phase products. The Mn oxide produced by a Pseudomonas species representative of soils and freshwaters was characterized as to composition, average Mn oxidation number, and N2 specific surface area. Electron microscopy, X-ray diffraction, and X-ray absorption near edge structure spectroscopy were applied to complement the physicochemical data with morphological and structural information. A series of synthetic Mn oxides also was analyzed by the same methods to gain better comparative understanding of the structure of the biogenic oxide. The latter was found to be a poorly crystalline layer type Mn(IV) oxide with hexagonal symmetry, significant negative structural charge arising from cation vacancies, and a relatively small number of randomly stacked octahedral sheets per particle. Its properties were comparable to those of δ-MnO2 (vernadite) and a poorly crystalline hexagonal birnessite (“acid birnessite”) synthesized by reduction of permanganate with HCl, but they were very different from those of crystalline triclinic birnessite. Overall, the structure and composition of the Mn oxide produced by P. putida were similar to what has been reported for other freshly precipitated Mn oxides in natural weathering environments, yielding further support to the predominance of biological oxidation as the pathway for Mn oxide formation. Despite variations in the degree of sheet stacking and Mn(III) content, all poorly crystalline oxides studied showed hexagonal symmetry. Thus, there is a need to distinguish layer type Mn oxides with structures similar to those of natural birnessites from the synthetic triclinic variety. We propose designating the unit cell symmetry as an addition to the current nomenclature for these minerals.  相似文献   
14.
The Carson River Superfund Site in west-central Nevada is an area of Hg-contaminated soil, sediment, water, air, and biola resulting from the amalgamation milling of Ag-Au ores of the Comstock lode worked approximately a century ago. In order to develop an understanding of the behavior, transport, and fate of Hg at this site, a technique was developed to estimate the proportions of total, elemental, exchangeable, organic, and sulfide Hg in soils, sediments, and tailings.Results of this analysis performed on active Carson River sediments indicate that Hg is selectively dissolved out of Hg-Au amalgam particles and subsequently adsorbed to fine-grained sediments which are then deposited in downstream, low-energy reaches of the Carson River and Labontan Reservoir. In the relatively more-reducing environment of the reservoir Hg appears to be converted, in large part, to relatively-insoluble HgS.The original elemental form of Hg released to the environment is the chemical form which is still dominant in most highly-contaminated soils, sediments, and tailings. Deeper, more-reducing soil horizons, however, appear to fix a significant portion of the Hg as HgS, analogous to the Lahontan Reservoir example described above. This fixation as HgS is documented to be largely limited to higher-sulfur areas where sulfide minerals from the Comstock ores increase the total sulfur concentrations of contaminated soils, sediments, and tailings.  相似文献   
15.
Major volcanogenic structures within the Marifil Formation allowed to determine the location of a claderas field that spreads along 400 kilometers. This field has at least three large calderas with diameters near to 100 kilometers, recognizable by regional distribution of associated dikes and rhyolite lava flows present at the caldera border that separates a monotonous ignimbritic plateau from a depressed (150 meters) inner volcanic collapsed caldera. The Marifil ignimbritic plateau cover more than 50,000 square kilometers with thicknesses that reach 800 meters. Associated with these plateau ignimbrites there is an important fluorite mineralization.  相似文献   
16.
 Cerro Panizos, a large caldera in the central Andes Mountains, produced two large dacitic ignimbrites at 7.9 Ma and 6.7 Ma and many andesitic and dacitic lava flows and domes. The older rhyodacitic Cienago Ignimbrite represents the most silicic magma erupted by the system. The younger, much larger volume dacitic Cerro Panizos Ignimbrite is very crystal-rich, containing up to 50% biotite, plagioclase, and quartz crystals in the pumice. It is weakly zoned, with most of the zoning apparent between two main cooling units. Major and most trace elements show little variation through the Cerro Panizos Ignimbrite, but the small range of composition is consistent with typical fractionation trends. Sr, Nd, and Pb isotopic ratios are very “crustal”, with initial 87Sr/86Sr values of 0.711 to 0.715, ɛNd values of –7.5 to –10.2, and nearly invariant Pb isotopic ratios (206Pb/204Pb=18.85, 207Pb/204Pb=15.67, and 208Pb/204Pb=38.80). The limited zonation observed in the Cerro Panizos Ignimbrite is explained by impeded crystal settling due to high crystal content. The magma body was a crystal-liquid mush before ascent to the pre-eruption crustal levels. Crystals formed, but did not separate easily from the magma. Limited fractionation of plagioclase and biotite may have occurred, but the composition was largely controlled by lower crustal MASH processes. AFC modeling shows that the Cerro Panizos magmas resulted from a mixture of roughly equal proportions of late Miocene mantle-derived basalts and melts from ∼1.0 Ga (Grenville age) lower crust. This occurred in a MASH zone in the lower crust, and set the crustal isotopic ratios observed in the Cerro Panizos magmas. The great thickening of the crust beneath the central Andes Mountains sent upper and middle crustal rock types to lower crustal (and deeper) depths, and this explains the “upper crustal” isotopic signatures of the Cerro Panizos rocks. Minor upper crustal assimilation of early Miocene volcanic or subvolcanic rocks produced much of the isotopic variation seen in the system. The nearly invariant high Pb isotopic values and high Pb concentrations indicate that Pb came almost entirely from the crustal source, and was little altered by any subsequent upper crustal assimilation. This Pb signature is isotopically similar to that of the southern Bolivian Tin Belt, suggesting a widely distributed Pb source. The great difference between compositions of Miocene and Quaternary central Andean volcanic rocks is explained by crustal thickening in early Miocene time leading to abundant lower crustal water and associated fluxed melting during the time of the earlier eruptions. The lower crust dried out considerably by Quaternary time, so less crustal component is present. Received: 22 December 1994 / Accepted: 13 September 1995  相似文献   
17.
Tropical forest mapping is one of the major environmental concerns at global and regional scales in which remote sensing techniques are firmly involved. This study examines the use of the variogram function to analyse forest cover fragmentation at different image scales. Two main aspects are considered here: (1) analysis of the spatial variability structure of the forest cover observed at three different scales using fine, medium and coarse spatial resolution images; and (2) the study of the relationship between rescaled images from the finest spatial resolution and those of the medium and coarse spatial resolutions. Both aspects are analysed using the variogram function as a basic tool to calculate and interpret the spatial variability of the forest cover. An example is presented for a Brazilian tropical forest zone using satellite images of different spatial resolutions acquired by Landsat TM (30 m), Resurs MSU (160 m) and ERS ATSR (1000 m). The results of this study contribute to establishing a suitable spatial resolution of remotely sensed data for tropical forest cover monitoring.  相似文献   
18.
In underground coal mining any increase in coal recovery rate is dependent on a decrease in pillar size. Backfilling is one way of reducing the required size of pillars and hence the volume of coal left underground. Therefore any comparisons made between a self-supported mine layout and backfill supported mine layout are based directly on pillar design. The most effective way to examine the effect of backfill on pillar support, and subsequently the rate of recovery, would be to incorporate the mechanisms of backfill support directly into the current design procedure for coal pillars. This paper presents a review of the mechanics of backfill support, a method of estimating the magnitude of that support based on earth pressure theory, and an example that incorporates backfill support into current coal pillar design.  相似文献   
19.
The synthetic amphibole Na0.95(Li0.95Mg1.05)Mg5Si8O22(OH)2 was studied in situ at high-T, using IR OH-stretching spectroscopy and synchrotron X-ray powder diffraction. At room-T the sample has P21 /m symmetry, as shown by the FTIR spectrum. It shows in the OH region two well-defined and intense absorptions at 3,748 and 3,712 cm−1, respectively, and two minor bands at 3,667 and 3,687 cm−1. The main bands are assigned to the two independent O–H groups in the primitive structure. The two minor bands evidencing the presence of small amount of vacant A-site (A0.05). With increasing T, these bands shift continuously and merge into a unique absorption at high temperature. A change as a function of increasing T is revealed by the evolution of the refined unit-cell parameters, whose trend shows a transition to C2/m at about 320–330°C. The spontaneous scalar strain, fitted with a tricritical 2–6 Landau potential, gives a T c of 325(10)°C (β parameter = 0.27). Comparison with the second-order P21 /mC2/m phase transition at 255°C for synthetic amphibole ANa0.8B(Na0.8Mg1.2)CMg5Si8O22(OH)2 indicates that the substitution of Na with Li at the B-sites strongly affects the thermodynamic character and the T c of the phase transition. The comparison of LNMSH amphiboles with cummingtonitic ones shows that the high-T thermodynamic behaviour is affected by A-site occupancy.  相似文献   
20.
Noble gas isotopes are widely used to elucidate the history of the rocks in which they have been trapped, either from distinct reservoirs or by accumulation following radioactive decay. To extract noble gases from their host rocks, stepwise heating is the most commonly used technique to deconvolve isotopically different components, e.g., atmospheric, in situ radiogenic, or excess radiogenic from mantle or crustal reservoirs. The accurate determination of the isotopic composition of these different components is of crucial importance, e.g., for ages obtained by 40Ar-39Ar stepheating plateaus. However, diffusion theory-based model calculations predict that the stepwise thermal extraction process from mineral phases induces isotope fractionation and, hence, adulterates the original composition. Such effects are largely unconsidered, as they are small and a compelling experimental observation is lacking. We report the first unequivocal evidence for significant mass fractionation of argon isotopes during thermal extraction, observed on shungite, a carbon-rich Precambrian sedimentary rock. The degree of fractionation, as monitored by 38Ar/36Ar and 40Ar/36Ar ratios, very well agrees with theoretical predictions assuming an inverse square root dependence of diffusion coefficient and atomic mass, resulting in easier extraction of lighter isotopes. Hence, subatmospheric 40Ar/36Ar ratios obtained for argon extracted at low temperatures may not represent paleoatmospheric argon. Shungite argon resembles modern atmospheric composition, but constraints on the timing of trapping appear difficult to obtain, as shungites are multicomponent systems.In 40Ar-39Ar stepwise heating, the isotope fractionation effect could cause systematic underestimations of plateau ages, between 0.15 and 0.4% depending on age, or considerably higher if samples contain appreciable atmospheric Ar. The magnitude of this effect is similar to the presently achieved uncertainties of this increasingly precise dating technique. Our results also indicate the importance of thermally activated diffusion as a possible fractionation mechanism, e.g., for hydrothermal gas exhalations, or for carbonaceous carrier phases such as “Q” in meteorites that have been suggested as carriers of highly fractionated noble gas residues from the early solar nebula.  相似文献   
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