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1.
Two processes are generally explained as causes of temporal changes in the stoichiometric silicon/nitrogen (Si/N) ratios of sinking particles and of nutrient consumption in the surface water during the spring diatom bloom: (1) physiological changes of diatom under the stress of photosynthesis of diatom and (2) differences of regeneration between silicon and nitrogen. We investigated which process plays an important role in these changes using a one-dimensional ecosystem model that explicitly represents diatom and the other non-silicious phytoplankton. The model was applied to station A7 (41°30′ N, 145°30′ E) in the western North Pacific, where diatom regularly blooms in spring. Model simulations show that the Si/N ratios of the flux exported by the sinking particles at 100 m depth and of nutrient consumptions in the upper 100 m surface water have their maxima at the end of the spring diatom bloom, the values and timings of which are significantly different from each other. Analyses of the model results show that the differences of regeneration between silicon and nitrogen mainly cause the temporal changes of the Si/N ratios. On the other hand, the physiological changes of diatoms under stress can hardly cause these temporal changes, because the effect of the change in the diatom's uptake ratio of silicon to nitrogen is cancelled by that in its sinking rate.  相似文献   
2.
A model based on that of Kishi et al. (2001) has been extended to 15 compartments including silicon and carbon cycles. This model was applied to Station A7 off Hokkaido, Japan, in the Northwestern Pacific. The model successfully simulated the observations of: 1. a spring bloom of diatoms; 2. large seasonal variations of nitrate and silicate concentrations in the surface water; and 3. large inter-annual variations in chlorophyll-a. It also reproduced the observed features of the seasonal variations of carbon dioxide partial pressure (pCO2)—a peak in pCO2 in winter resulting from deep winter convection, a rapid decrease in pCO2 as a result of the spring bloom, and an almost constant pCO2 from summer through fall (when the effect of increasing temperature cancels the effect of biological production). A comparison of cases with and without silicate limitation shows that including silicate limitation in the model results in: 1. decreased production by diatoms during summer; and 2. a transition in the dominant phytoplankton species, from diatoms to other species that do not take up silicate. Both of these phenomena are observed at Station A7, and our results support the hypothesis that they are caused by silicate limitation of diatom growth. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
3.
Mesozoic brackish-water bivalve faunas in Japan diversified in three steps: at the beginning of the Early Jurassic, Early and Late Cretaceous. The Hettangian Niranohama Fauna in northeastern Honshu represents the establishment of a heterodont-dominated brackish-water fauna that persisted until the early Late Cretaceous. No similar composition is known from the Triassic. The infauna consists mostly of non-siphonate and some short-siphonate heterodonts, while the epifauna is represented by diverse pteriomorphian families. In the Early Cretaceous Tetori Group in central Honshu, the long-siphonate heterodonts Tetoria (Corbiculidae) and the semi-infaunal soft-bottom oyster Crassostrea appeared. The evolutionary diversification of the latter, known as the most important element of modern brackish-water faunas, may thus originate at that time. In the early Late Cretaceous (Cenomanian) of the Goshoura and Mifune Groups in west Kyushu, several euryhaline deep-burrowing heterodont families, such as Veneridae and Tellinidae, further diversified in the brackish and marine environments. The Late Cretaceous is characterized by massive shell biolithic beds in which large Crassostrea species are common, a feature common for Cenozoic brackish-water faunas. The long-term changes in the composition of the brackish-water faunas in Japan represents thus an evolutionary record, irrespective of the severe physiological and environmental conditions imposed on the highly conservative nature of the fauna.  相似文献   
4.
The fruticose lichen Cetrariella delisei is among the dominant lichen species in the deglaciated High Arctic areas of Svalbard. As part of a study of carbon cycling in the High Arctic, we aimed to estimate the primary production of lichen in a deglaciated area in Ny-Ålesund, Svalbard (79° N), by examining the effects of abiotic factors on the net photosynthesis ( Pn ) and dark respiration ( R ) rates of C. delisei . Experiments were conducted in the snow-free season of 2000 using an open-flow gas exchange system with an infrared gas analyser. Positive photosynthetic activities were observed on rainy days or soon after rainfall when the thallus water content was high, whereas photosynthetic activities dropped below the detectable limit on clear days because of the low thallus water content. Under a sufficiently high thallus water content and close to light saturation, Pn was nearly constant over a wide temperature range of 4–20 °C, while R increased with increasing temperature. We constructed a model for estimating the net primary production ( NPP ) of lichen based on the relationships between abiotic factors and the CO2 exchange rate. The mean, minimum and maximum NPP values in the snow-free season, estimated using meteorological data obtained from 1995–2003, were 5.1, 1.0 and 8.4 g dry wt. m−2 snow-free season−1, respectively. These results suggest that NPP is highly variable and the contribution of lichen to carbon input is small compared with that of vascular plants and mosses in the study site.  相似文献   
5.
2500年来艾比湖的环境演变信息   总被引:22,自引:9,他引:22  
通过对艾比湖缘1,8m浅孔的沉积相和孢粉组合,结合14C测年资料分析。指出近2500年来艾比湖的沉积环境总体是比较稳定的,但由于气候波动引起艾比湖水位曾发生较明显的变化。约在公元前300~400年,是艾比湖面积缩小时期;约公元前300—公元300年,即东周末至西晋,是艾比湖水位较高时期;约公元300—1400年,即东晋至15世纪初,是艾比湖的高水位时期;约15世纪初至17世纪中是艾比湖的水位下降期,但水位比现代仍然高;约17世纪中至19世纪初的小冰期是艾比湖的水位上升期。研究还提供了历史时期湖泊的盐度变化和湖周发生大火的信息。  相似文献   
6.
The convective boundary layer (CBL) with a wide range of stability is simulated experimentally using a thermally stratified wind tunnel, and numerically by direct numerical simulation (DNS). The turbulence structures and flow characteristics of various CBL flows, capped by a strong temperature inversion and affected by surface shear, are investigated. The various vertical profiles of turbulence statistics similar to those from the observed CBL in the field are successfully simulated in both the wind-tunnel experiment and in DNS. The comparison of the wind-tunnel data and DNS results with those of atmospheric observations and water-tank studies shows the crucial dependence of the turbulence statistics in the upper part of the layer on the strength of the inversion layer, as well as the modification of the CBL turbulence regime by the surface shear.  相似文献   
7.
Abstract. The Nankai Trough runs along the Japanese Islands, where extensive BSRs have been recognized in its forearc basins. High resolution seismic surveys and site-survey wells undertaken by the MITI have revealed the gas hydrate distribution at a depth of about 290 mbsf. The MITI Nankai Trough wells were drilled in late 1999 and early 2000. The highlights were successful retrievals of abundant gas hydrate-bearing cores in a variety of sediments from the main hole and the post survey well-2, keeping the cored gas hydrate stable, and the obtaining of continuous well log data in the gas hydrate-dominant intervals from the main hole, the post survey well-1 and the post survey well-3. Gas-hydrate dominant layers were identified at the depth interval from 205 to 268 mbsf. Pore-space hydrate, very small in size, was recognized mostly filling intergranular pores of sandy sediments. Anomalous chloride contents in extracted pore water, core temperature depression, core observations as well as visible gas hydrates confirmed the presence of pore-space hydrates within moderate to thick sand layers. Gas hydrate-bearing sandy strata typically were 10 cm to a meter thick with porosities of about 40 %. Gas hydrate saturations in most hydrate-dominant layers were quite high, up to 90 % pore saturation.
All the gas hydrate-bearing cores were subjected to X-ray CT imagery measurements for observation of undisturbed sedimentary textures and gas-hydrate occurrences before being subjected to other analyses, such as (1) petrophysical properties, (2) biostratigraphy, (3) geochemistry, (4) microbiology and (5) gas hydrate characteristics.  相似文献   
8.
9.
More than 30 years of chemical oxygen demand (COD) and dissolved inorganic nitrogen (DIN) data for the inner area of the Ariake Sea were analyzed with a box model to show the changes in the average seasonal budget and the decadal-scale variation during the summer. The COD peaked in August and March on average. This summertime peak can be explained by an enhanced riverine load and increased primary production. The peak in March suggested additional organic matter production. There were also two peaks in DIN concentration on average: a summertime peak that could be explained by an enhanced riverine load, and a peak in December that was more complicated to explain. From the 1970s to the early 1990s, the bottom water in this area became increasingly hypoxic due to increased COD during the summer, even though there were minimal increases in terrestrial COD and nutrient loads and there were tidal flats covering a widespread area during this period. The increase in COD was caused by increased net ecosystem production, which was due to enhanced primary production induced by an increased freshwater residence time and decreased bivalve grazing. There was a negative feedback control in which hypoxia progressively increased, leading to declines in bivalve biomass, which in turn decreased the grazing pressure limiting primary production, meaning that primary production increased and the area became even more hypoxic. The net DIN production decreased during the 1980s and the 1990s. This was consistent with the change in net ecosystem production according to the COD.  相似文献   
10.
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