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1.
Uniform models for the Earth–ionosphere cavity are considered with particular attention to the physical properties of the ionosphere for the extremely low frequency (ELF) range. Two consistent features have long been recognized for the range: the presence of two distinct altitude layers of maximum energy dissipation within the lower ionosphere, and a “knee”-like change in the vertical conductivity profile representing a transition in dominance from ion-dominated to electron-dominated conductivity. A simplified two-exponential version of the Greifinger and Greifinger (1978) technique widely used in ELF work identifies two slopes in the conductivity profile and, providing accurate results in the ELF communication band (45–75 Hz), simulates too flat a frequency dependence of the quality factor within the Schumann resonance frequency range (5–40 Hz). The problem is traced to the upward migration, with frequency increasing, of the lower dissipation layer through the “knee” region resulting in a pronounced decrease of the effective scale height for conductivity. To overcome this shortcoming of the two-exponential approximation and still retain valuable model analyticity, a more general approach (but still based on the Greifinger and Greifinger formalism) is presented in the form of a “knee” model whose predictions for the modal frequencies, the wave phase velocities and the quality factors reasonably represent observations in the Schumann resonance frequency range. 相似文献
2.
Ore-placer shows of platinum group elements in the areal of North-Asian Superplume derivations(South-East Russia) 下载免费PDF全文
The sources of large and unique platinum-metal placers were the zonal alkali-ultrabasic massifs be coming active in the retaceous ime that gravitated to the periphery of the areal of the North-Asian Su... 相似文献
3.
Cornel E. J. de Ronde Gary J. Massoth David A. Butterfield Bruce W. Christenson Junichiro Ishibashi Robert G. Ditchburn Mark D. Hannington Robert L. Brathwaite John E. Lupton Vadim S. Kamenetsky Ian J. Graham Georg F. Zellmer Robert P. Dziak Robert W. Embley Vesselin M. Dekov Frank Munnik Janine Lahr Leigh J. Evans Ken Takai 《Mineralium Deposita》2011,46(5-6):541-584
Brothers volcano, of the Kermadec intraoceanic arc, is host to a hydrothermal system unique among seafloor hydrothermal systems known anywhere in the world. It has two distinct vent fields, known as the NW Caldera and Cone sites, whose geology, permeability, vent fluid compositions, mineralogy, and ore-forming conditions are in stark contrast to each other. The NW Caldera site strikes for ??600?m in a SW?CNE direction with chimneys occurring over a ??145-m depth interval, between ??1,690 and 1,545?m. At least 100 dead and active sulfide chimney spires occur in this field and are typically 2?C3?m in height, with some reaching 6?C7?m. Their ages (at time of sampling) fall broadly into three groups: <4, 23, and 35?years old. The chimneys typically occur near the base of individual fault-controlled benches on the caldera wall, striking in lines orthogonal to the slopes. Rarer are massive sulfide crusts 2?C3?m thick. Two main types of chimney predominate: Cu-rich (up to 28.5?wt.% Cu) and, more commonly, Zn-rich (up to 43.8?wt.% Zn). Geochemical results show that Mo, Bi, Co, Se, Sn, and Au (up to 91?ppm) are correlated with the Cu mineralization, whereas Cd, Hg, Sb, Ag, and As are associated with the dominant Zn-rich mineralization. The Cone site comprises the Upper Cone site atop the summit of the recent (main) dacite cone and the Lower Cone site that straddles the summit of an older, smaller, more degraded dacite cone on the NE flank of the main cone. Huge volumes of diffuse venting are seen at the Lower Cone site, in contrast to venting at both the Upper Cone and NW Caldera sites. Individual vents are marked by low-relief (??0.5?m) mounds comprising predominately native sulfur with bacterial mats. Vent fluids of the NW Caldera field are focused, hot (??300°C), acidic (pH????2.8), metal-rich, and gas-poor. Calculated end-member fluids from NW Caldera vents indicate that phase separation has occurred, with Cl values ranging from 93% to 137% of seawater values. By contrast, vent fluids at the Cone site are diffuse, noticeably cooler (??122°C), more acidic (pH?1.9), metal-poor, and gas-rich. Higher-than-seawater values of SO4 and Mg in the Cone vent fluids show that these ions are being added to the hydrothermal fluid and are not being depleted via normal water/rock interactions. Iron oxide crusts 3?years in age cover the main cone summit and appear to have formed from Fe-rich brines. Evidence for magmatic contributions to the hydrothermal system at Brothers includes: high concentrations of dissolved CO2 (e.g., 206?mM/kg at the Cone site); high CO2/3He; negative ??D and ??18OH2O for vent fluids; negative ??34S for sulfides (to ?4.6??), sulfur (to ?10.2??), and ??15N2 (to ?3.5??); vent fluid pH values to 1.9; and mineral assemblages common to high-sulfidation systems. Changing physicochemical conditions at the Brothers hydrothermal system, and especially the Cone site, occur over periods of months to hundreds of years, as shown by interlayered Cu?+?Au- and Zn-rich zones in chimneys, variable fluid and isotopic compositions, similar shifts in 3He/4He values for both Cone and NW Caldera sites, and overprinting of ??magmatic?? mineral assemblages by water/rock-dominated assemblages. Metals, especially Cu and possibly Au, may be entering the hydrothermal system via the dissolution of metal-rich glasses. They are then transported rapidly up into the system via magmatic volatiles utilizing vertical (??2.5?km long), narrow (??300-m diameter) ??pipes,?? consistent with evidence of vent fluids forming at relatively shallow depths. The NW Caldera and Cone sites are considered to represent stages along a continuum between water/rock- and magmatic/hydrothermal-dominated end-members. 相似文献
4.
The effect of crystal structure relaxation in oxygen-based Cr3+-containing minerals on the crystal field stabilization energy (CFSE) is considered. It is shown that the dependence of
\textCFSE\textCr 3+ {\text{CFSE}}_{{{\text{Cr}}^{ 3+ } }} , which is found from optical absorption spectra, on the average interatomic distances is described by the power function
with a negative exponent
c \mathord