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We have calculated a grid of empirically well tested evolutionary tracks with masses M between 0.5 and 50 M⊙, spaced by approximately 0.1 in log M , and with metallicities Z  = 0.0001, 0.0003, 0.001, 0.004, 0.01, 0.02 and 0.03. We use a robust and fast evolution code with a self-adaptive non-Lagrangian mesh, which employs the mixing-length theory but treats convective mixing as a diffusion process, solving simultaneously for the structure and the chemical composition. The hydrogen and helium abundances are chosen as functions of the metallicity: X  = 0.76 − 3.0 Z Y  = 0.24 + 2.0 Z .   Two sets of models were computed, one without and one with a certain amount of enhanced mixing or 'overshooting'. This amount has been empirically chosen by means of various sensitive tests for overshooting: (1) the luminosity of core helium burning (blue loop) giants of well-known mass, (2) the width of the main sequence as defined by double-lined eclipsing binaries with well-measured masses and radii, and (3) the shape and implied stellar distribution of isochrones of various open clusters. The first two tests have been the subject of previous papers, the third test is discussed in this paper. On the basis of these tests, we recommend the use of the overshooting models for masses above about 1.5M ⊙.   We describe here the characteristics of the models, the procedure for constructing isochrones for arbitrary age and metallicity from the models, and the performance of these isochrones for several intermediate-age and old open clusters. All original models are available in electronic form and we describe the means by which they may be obtained.  相似文献   
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The paper presents recent achievements in evaluations of site-dependent seismic hazard in Romania and the capital city of Bucharest caused by the Vrancea focal zone (SE-Carpathians). The zone is characterized by a high rate of occurrence of large earthquakes in a narrow focal volume at depths 60–170 km. The database that was used for the hazard evaluation includes parameters of seismicity, ground-motion source scaling and attenuation models (Fourier amplitude spectra), and site-dependent spectral amplification functions. Ground-motion characteristics were evaluated on the basis of several hundred records from more than 120 small magnitude (M 3.5–5) earthquakes occurred in 1996–2001 and a few tens of acceleration records obtained during four large (M 7.4, 7.2, 6.9 and 6.3) earthquakes. The data provide a basis for probabilistic seismic hazard assessment in terms of peak ground acceleration, peak spectral acceleration and MSK intensity using Fourier amplitude spectra for various exceedance probabilities or average return periods. It has been shown that the influence of geological factors plays very important role in distribution of earthquake ground-motion parameters along the territory of Romania.  相似文献   
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We present the regional ground-motion prediction equations for peak ground acceleration (PGA), peak ground velocity (PGV), pseudo-spectral acceleration (PSA), and seismic intensity (MSK scale) for the Vrancea intermediate depth earthquakes (SE-Carpathians) and territory of Romania. The prediction equations were constructed using the stochastic technique on the basis of the regional Fourier amplitude spectrum (FAS) source scaling and attenuation models and the generalised site amplification functions. Values of considered ground motion parameters are given as the functions of earthquake magnitude, depth and epicentral distance. The developed ground-motion models were tested and calibrated using the available data from the large Vrancea earthquakes. We suggest to use the presented equations for the rapid estimation of seismic effect after strong earthquakes (Shakemap generation) and seismic hazard assessment, both deterministic and probabilistic approaches.  相似文献   
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Atmospheric concentrations of ca. 250 C6–C15 hydrocarb on and C4–C12 oxygenated volatile organic compounds (VOC) including alkanes, benzene and alkyl benzenes, monoterpenes and aldehydes were measured in August 1994 during the POPCORN campaign (POPCORN = Photo-Oxidant formation by Plant emitted Compounds and OH Radicals in North-Eastern Germany). About 80 substances together contributed 90% of the atmospheric carbon in this range of molecular weight. During this field campaign VOC-emissions from several crop and tree species and the ambient concentrations of CO, C2–C7 non-methane hydrocarbons (NMHC), C1 and C2 aldehydes, nitrogen oxides, ozone and hydroxyl-radicals (OH) were also measured. These data were used to interpret the VOC measurements presented here. The on-line GC–MS used for the VOC measurements combines adsorptive sampling with thermal desorption and GC–MS analysis in an automated system. Internal standards were used to quantify the measurements. Ozone was destroyed prior to the sample preconcentration through the gas phase reaction with NO. Aromatic compounds like benzene, toluene and xylenes were the most abundant compound class among the measured substances, -pinene and 3-carene, most probably originating from pineforests ca. 1 km away from the measuring site, were the most abundant monoterpenes. The highest mixing ratios of most compounds were measured in nights with strong inversion situations. The toluene mixing ratios then reached 630 pptv; -pinene mixing ratios went up to 430 pptv. The median of all toluene and -pinene measurements during the campaign was 125 pptv or 22 pptv, respectively. These values are on the lower end of ambient measurements reported for continental sites. In most samples also n-pentanal, n-hexananl, n-nonanal and n-undecanal were present. Median mixing ratios were 9, 16, 14 and 8 pptv, respectively. Emission studies indicate that these highly reactive compounds are most probably emitted from maize. It is shown by a simple first order approach that the potential for ozone formation during the POPCORN campaign was roughly equal for anthropogenic and biogenic VOC. From measured concentrations of ozone, OH-radicals, methane, CO, C2–C15 nonmethane hydrocarbons (NMHC) and C5–C11 aldehydes a photochemical production of ozone in the order of 3.5 ppb/h can be estimated. Apart from formaldehyde and acetaldehyde, which are at least partly products of VOC oxidation, the substance group with the largest contribution to the VOC turnover are the monoterpenes. They contribute ca. 30%. However, the mechanism of terpene oxidation is very complex and presently only partly understood. Thus the actual contribution of monoterpenes to ozone formation is very uncertain. Other measured compound classes such as light alkenes, alkanes, aromatics, and C5–C11 aldehydes contribute each between 10% and 15% to ozone formation. The measuring site was not influenced directly from strong biogenic or anthropogenic sources, and the results obtained during the POPCORN campaign can be regarded as a typical picture of a remote rural central European environment.  相似文献   
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