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861.
There have been many studies of the retail industry in recent years, and of the impact that retailing has had on the spatial arrangement of urban areas and on consumer behaviour. Little attention has been paid, however, to employment in retailing, which is disturbing in view of its growing importance and its rapidly changing nature and composition. This paper examines the nature of the broad structural changes within the industry, and investigates their spatial consequences through a case study of employment generation within a system of suburban retail centres in Canberra, Australia. It is shown that the evolution of suburban centres, particularly those of a regional variety, has had an important and enriching impact on the suburban labour market. The regional centres are also seen to be the focus of the major structural employment changes currently affecting the retail industry. This has some important implications for urban planning. 相似文献
862.
863.
864.
Lawrence Grossman John M. Allen Glenn J. MacPherson 《Geochimica et cosmochimica acta》1980,44(2):211-216
The black inclusion from the Krymka LL3 chondrite previously found to contain ‘mysterite’ by Lewiset al. (1979) belongs to a hitherto unknown class of carbonaceous chondrites. Its olivine and pyroxene compositions. Fo 97–99 and En 96, respectively, are characteristic of carbonaceous chondrites and its plagioclase composition. An 100, is characteristic of C3's. It contains a peculiar group of Co-, Cr-rich metal grains whose compositions are similar, but not identical, to those in C2 chondrites and which also bear some similarities to those in Renazzo. Its weight ratios of total and are 0.74 and 1.43, respectively, and its atomic ratio of is 10.7, exactly the same as in carbonaceous chondrites. Its bulk chemical composition is very close to that of the Murchison C2 chondrite. The association of mysterite with a special type of carbonaceous chondrite material suggests that mysterite formed by low-temperature condensation in a different region of the nebula from other carbonaceous chondrites. 相似文献
865.
The stick-slip of frictional sliding depends not only on material properties but also on the elastic and inertial properties of the loading system. To compare data from different testing machines or to apply them to the problem of natural seismogenic faulting, one must account for the differences in stiffness and mass. We develop a simple mechanical model to describe the stick-slip oscillation during frictional sliding in a triaxial-compression machine. The experimental system, the loading frame and rock specimen with precut sliding surface, is divided into two subsystems across this surface. The model is based upon two key assumptions: the kinetic friction is constant regardless of the relative motion of the subsystems, and the elastic restoring force is uniform throughout each subsystem. The first assumption leads to the decoupling of the subsystems, and the behavior of each becomes mathematically analogous to that of a simple spring/mass/slider-block model, owing to the second assumption. The theory agrees well with the experimental data from the dynamic measurements of stick-slip. The displacement-time function is of cosine form, the rise time of stick-slip is constant, and the relation between force drop and average displacement rate is linear. From this model we argue that the differences in the frictional behavior of experimental fault-gouges may indeed be ascribed to differences in the material properties of their specimens because the elastic and inertial properties of a particular testing machine are little influenced by the specimen itself, so long as all specimens are of about the same size. However, interlaboratory correlations may well be invalid unless machine effects are properly accounted for. 相似文献
866.
867.
Richard B. Wheeler John B. Anderson Rudy R. Schwarzer Claudia L. Hokanson 《Environmental Geology》1980,3(3):163-175
Sediments are the ultimate sink for contaminants in the marine environment, and physical processes of sedimentation influence
the distribution and accumulation of these contaminants. Evaluation of contaminant levels in sediments is one approach to
assessing environmental impact; data interpretation depends on consideration of sediment texture and mineralogy, however,
which profoundly influence chemical composition. In this study, comparison of potentially contaminated sediments from the
production field with control populations was done only within the context of similar (as to texture and organic carbon and
carbonate content) sample groups as determined by cluster analysis. Ba, Cd, and Sr are identified as contaminants. Supported
by the identification of a well-crystallized expandable clay—possibly bentonite—drilling fluids are a potential source of
Ba. Ba and Sr may be unnaturally high because of their abundance in discharged produced formation waters, but may also be
naturally controlled by the unique faunal assemblage associated with the structures. Cd is probably derived from corrosion
of the structures and assorted debris on the seafloor. In general, contamination is limited to an area within 100 m of the
platforms. Furthermore, substantial erosion around platforms has probably effectively removed and dispersed the bulk of the
contaminants introduced into the marine environment by the offshore exploration/production operations. 相似文献
868.
William A. Bassett John M. Bird Maura S. Weathers D.L. Kohlstedt 《Physics of the Earth and Planetary Interiors》1980,23(4):255-261
Josephinite, a complex, metal-bearing rock from the region of the Josephine Peridotite in southwest Oregon, contains FeNiCo metal alloy phases having exsolution textures. Scanning and transmission electron microscopy have revealed Widmanstaetten patterns in which the lamellae are polysynthetically twinned, ordered, face-centered-cubic FeNi3 surrounded by untwinned, ordered, face-centered-cubic FeNi3 and body-centered-cubic FeCo. These exsolution textures require a temperature in excess of 500°C for their formation. This is consistent with a mantle derivation of josephinite prior to obduction of the peridotite in one of the Klamath ophiolites. 相似文献
869.
Rare earth element distribution in some hydrothermal minerals: evidence for crystallographic control 总被引:1,自引:0,他引:1
Rare earth element (REE) abundances were measured by neutron activation analysis in anhydrite (CaSO4), barite (BaSO4), siderite (FeCO3) and galena (PbS). A simple crystal-chemical model qualitatively describes the relative affinities for REE substitution in anhydrite, barite, and siderite. When normalized to ‘crustal’ abundances (as an approximation to the hydrothermal fluid REE pattern), log REE abundance is a surprisingly linear function of (ionic radius of major cation—ionic radius of REE)2 for the three hydrothermal minerals, individually and collectively. An important exception, however, is Eu, which is anomalously enriched in barite and depleted in siderite relative to REE of neighboring atomic number and trivalent ionic radius. In principle, REE analyses of suitable pairs of co-existing hydrothermal minerals, combined with appropriate experimental data, could yield both the REE content and the temperature of the parental hydrothermal fluid.The REE have only very weak chalcophilic tendencies, and this is reflected by the very low abundances in galena—La, 0.6 ppb; Sm, 0.06 ppb; the remainder are below detection limits. 相似文献
870.
Chemical equilibrium between sodium-aluminum silicate minerals and chloride bearing fluid has been experimentally determined in the range 500–700°C at 1 kbar, using rapid-quench hydrothermal methods and two modifications of the Ag + AgCl acid buffer technique. The temperature dependence of the thermodynamic equilibrium constant (K) for the reaction Albite Andalusite Qtz. can be described by the following equation: log k = ?4.437 + 5205.6/T(K) The data from this study are consistent with experimental results reported by Montoya and Hemley (1975) for lower temperature equilibria defined by the assemblages albite + paragonite + quartz + fluid and paragonite + andalusite + quartz + fluid. Values of the equilibrium constants for the above reactions were used to estimate the difference in Gibbs free energy of formation between NaClo and HClo in the range 400–700°C and 1–2 kbar. Similar calculations using data from phase equilibrium studies reported in the literature were made to determine the difference in Gibbs free energy of formation between KClo and HClo. These data permit modelling of the chemical interaction between muscovite + kspar + paragonite + albite + quartz assemblages and chloride-bearing hydrothermal fluids. 相似文献