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1.
A method of structural damage identification using harmonic excitation force is presented. It considers the effects of both measurement and modelling errors in the baseline finite element model. Damage that accompanies changes in structural parameters can be estimated for a damaged structure from the change between measured vibration responses and ones calculated from the analytical model of the intact structure. In practice, modelling errors exist in the analytical model due to material and geometric uncertainties and a reduction in the degrees of freedom as well as measurement errors, making identification difficult. To surmount these problems, bootstrap hypothesis testing, which enables statistical judgment without information about these errors, was introduced. The method was validated by numerical simulation using a three‐dimensional frame structure and real vibration data for a three‐storey steel frame structure. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
2.
Ocean Color Satellite Imagery and Shipboard Measurements of Chlorophyll a and Suspended Particulate Matter Distribution in the East China Sea 总被引:1,自引:0,他引:1
Satellite-derived ocean color data of Coastal Zone Color Scanner (CZCS) on board the Nimbus-7 and Ocean Color and Temperature Scanner (OCTS) on board the Advanced Earth Observing Satellite (ADEOS) are jointly used with historical in situ data to examine seasonal and spatial distributions of chlorophyll a (Chl-a) and suspended particulate matter (SPM) concentrations in the East China Sea. Ocean color imagery showed that Chl-a concentrations on the continental shelf were higher than those of the Kuroshio area throughout the year. Satellite-derived Chl-a concentrations are generally in good accordance with historical in situ values during spring through autumn (although no shipboard in situ measurement was conducted at nearshore areas). In contrast, ocean color imagery in winter indicated high Chl-a concentrations (4–10 mg m–3) on the continental shelf where bottom depth was less than 50 m when surface water was turbid (2–72 g m–3 of SPM at surface), while historical in situ values were usually less than 1 mg m–3. This suggests that resuspended bottom sediment due to wind-driven mixing and winter cooling is responsible for the noticeable overestimation of satellite-derived Chl-a concentrations. The algorithm for ocean color needs to be improved urgently for turbid water. 相似文献
3.
The characteristics of the ratios between cadmium (Cd) and phosphorus (P) in settling particles collected from the Okinawa
Trough in the East China Sea were examined using a sediment trap, moored at a depth of 811 m for one year. The Cd/P ratios
varied within a narrow range throughout the year, in spite of the large seasonal change in the total dry mass, Cd, and P fluxes.
The average Cd/P ratio of settling particles was 0.062 (nmol/μmol), which was obviously lower than that of surface seawater around the study site (0.16). This lower ratio in the Okinawa
Trough particles collected using the 811 m-moored trap certainly reflected the mixture of biologically produced organic matter
around the study site and other components that were mainly transported as lateral flux from the shelf edge and slope area
of the East China Sea. 相似文献
4.
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6.
Single crystals of akermanite (Ca1–x
Sr
x
)2Co-Si2O7 solid solution were grown in nitrogen by the floating zone method using a lamp-image furnace. The grown crystals were 6 mm in diameter by 50 mm in length. Microprobe analyses indicate uniform strontium content x except in the initially crystallized part. Synthetic crystals with x from 0.0 to 0.3 give, at room temperature, satellite reflections and circular diffuse scatterings in the electron diffraction pattern, which are related to an incommensurate phase and microdomains, respectively. With increasing Sr content the wavelength of a modulation increases and the intensity of satellites decreases, but the intensity of circular diffuse scattering increases up to x=0.15 and then decreases until eventually the satellites and the circular diffuse scatterings disappear at x = 0.3. The circular diffuse scattering is explained by the cluster model for the transition state, proposed by De Ridder et al. (1976). 相似文献
7.
Yoko Tsushima S. Emori T. Ogura M. Kimoto M. J. Webb K. D. Williams M. A. Ringer B. J. Soden B. Li N. Andronova 《Climate Dynamics》2006,27(2-3):113-126
We have conducted a multi-model intercomparison of cloud-water in five state-of-the-art AGCMs run for control and doubled carbon dioxide climates. The most notable feature of the differences between the control and doubled carbon dioxide climates is in the distribution of cloud-water in the mixed-phase temperature band. The difference is greatest at mid and high latitudes. We found that the amount of cloud ice in the mixed phase layer in the control climate largely determines how much the cloud-water distribution changes for the doubled carbon dioxide climate. Therefore evaluation of the cloud ice distribution by comparison with data is important for future climate sensitivity studies. Cloud ice and cloud liquid both decrease in the layer below the melting layer, but only cloud liquid increases in the mixed-phase layer. Although the decrease in cloud-water below the melting layer occurs at all latitudes, the increase in cloud liquid in the mixed-phase layer is restricted to those latitudes where there is a large amount of cloud ice in the mixed-phase layer. If the cloud ice in the mixed-phase layer is concentrated at high latitudes, doubling of carbon dioxide might shift the center of cloud water distribution poleward which could decrease solar reflection because solar insolation is less at higher latitude. The magnitude of this poleward shift of cloud water appears to be larger for the higher climate sensitivity models, and it is consistent with the associated changes in cloud albedo forcing. For the control climate there is a clear relationship between the differences in cloud-water and relative humidity between the different models, for both magnitude and distribution. On the other hand the ratio of cloud ice to cloud-water follows the threshold temperature which is determined in each model. Improved measurements of relative humidity could be used to constrain the modeled representation of cloud water. At the same time, comparative analysis in global cloud resolving model simulations is necessary for further understanding of the relationships suggested in this paper. 相似文献
8.
Aaron J. Beck Yoko Tsukamoto Antonio Tovar-Sanchez Miguel Huerta-Diaz Henry J. Bokuniewicz Sergio A. Sañudo-Wilhelmy 《Applied Geochemistry》2007
Seasonal (Spring and Summer 2002) concentrations of dissolved (<0.22 μm) trace metals (Ag, Al, Co, Cu, Mn, Ni, Pb), inorganic nutrients (NO3, PO4, Si), and DOC were determined in groundwater samples from 5 wells aligned along a 30 m shore-normal transect in West Neck Bay, Long Island, NY. Results show that significant, systematic changes in groundwater trace metal and nutrient composition occur along the flowpath from land to sea. While conservative mixing between West Neck Bay water and the groundwaters explains the behavior of Si and DOC, non-conservative inputs for Co and Ni were observed (concentration increases of 10- and 2-fold, respectively) and removal of PO4 and NO3 (decreases to about half) along the transport pathway. Groundwater-associated chemical fluxes from the aquifer to the embayment calculated for constituents not exhibiting conservative behavior can vary by orders of magnitude depending on sampling location and season (e.g. Co, 3.4 × 102– 8.2 × 103 μmol d−1). Using measured values from different wells as being representative of the true groundwater endmember chemical composition also results in calculation of very different fluxes (e.g., Cu, 6.3 × 103 μmol d−1 (inland, freshwater well) vs. 2.1 × 105 μmol d−1(seaward well, S = 17 ppt)). This study suggests that seasonal variability and chemical changes occurring within the subterranean estuary must be taken into account when determining the groundwater flux of dissolved trace metals and nutrients to the coastal ocean. 相似文献
9.
Toshiyuki Wakatsuki Hisao Furukawa Kazutake Kyuma 《Geochimica et cosmochimica acta》1977,41(7):891-902
Sixteen alluvial and terrace soils from Japan and Thailand were separated into six fractions ; an amorphous sesquioxide and combined organic matter fraction, crystalline sesquioxides, clay, silt, fine sand and coarse sand. Content of ten major and minor elements in these six fractions was analyzed; SiO2, A12O3, Fe2O3, MgO, CaO, K2O, TiO2, Rb2O and SrO were determined by X-ray fluorescence spectrometry, and Na2O was determined by neutron activation analysis. The clay, silt, fine sand and coarse sand mineralogy were estimated semi-quantitatively by X-ray diffraction methods.We propose three indices of geochemical maturity for the soils and test their usefulness as measures of the degree of weathering. Three concomitant factors are proposed to measure the relative resistate, hydrolyzate and oxidate nature of the major elements in the soils. 相似文献
10.
Associations of organic matter with minerals in Tagish Lake meteorite via high spatial resolution synchrotron‐based FTIR microspectroscopy 下载免费PDF全文
We have investigated spatial and spectral associations between mineral species and organic matter in the Tagish Lake meteorite. Synchrotron‐based infrared microspectroscopy allowed us to spatially locate specific organic and inorganic compounds within multiple Tagish Lake grains with high spatial resolution. Generated two‐dimensional infrared maps present strong spatial association between aliphatic C‐H and OH in phyllosilicates in Tagish Lake grains. These observations indicate possible roles of phyllosilicates for the formation, evolution, and preservation of organic matter. Infared spectra of all studied Tagish Lake grains show a strong carbonate band, which also shows a weak but positive correlation with organic matter in some grains. However, intergrain correlation was not observed between carbonates and organics, which is likely due to the difference of carbonate occurrence, e.g., presence of larger grains or intergrowth of carbonates on phyllosilicates. Possible scenarios further explaining the observed associations of organics with phyllosilicates and carbonates are presented. 相似文献