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961.
We tested the hypothesis that increased growth of salmon during early marine life contributed to greater survival and abundance of salmon following the 1976/1977 climate regime shift and that this, in turn, led to density-dependent reductions in growth during late marine stages. Annual measurements of Bristol Bay (Bering Sea) and Chignik (Gulf of Alaska) sockeye salmon scale growth from 1955 to 2002 were used as indices of body growth. During the first and second years at sea, growth of both stocks tended to be higher after the 1976–1977 climate shift, whereas growth during the third year and homeward migration was often below average. Multiple regression models indicated that return per spawner of Bristol Bay sockeye salmon and adult abundance of western and central Alaska sockeye salmon were positively correlated with growth during the first 2 years at sea and negatively correlated with growth during later life stages. After accounting for competition between Bristol Bay sockeye and Asian pink salmon, age-specific adult length of Bristol Bay salmon increased after the 1976–1977 regime shift, then decreased after the 1989 climate shift. Late marine growth and age-specific adult length of Bristol Bay salmon was exceptionally low after 1989, possibly reducing their reproductive potential. These findings support the hypothesis that greater marine growth during the first 2 years at sea contributed to greater salmon survival and abundance, which in turn led to density-dependent growth during later life stages when size-related mortality was likely lower. Our findings provide new evidence supporting the importance of bottom-up control in marine ecosystems and highlight the complex dynamics of species interactions that continually change as salmon grow and mature in the ocean.  相似文献   
962.
In this study, seasonal and annual variability in the use of estuarine and ocean beaches by young-of-the-year bluefish, Pomatomus saltatrix, was evaluated by indices of abundance in coastal areas of southern New Jersey (1998–2000). Biological and physical factors measured at specific sites were correlated with bluefish abundance to determine the mechanisms underlying habitat selection. In addition, integrative and discrete indicators of bluefish growth were used to examine spatio-temporal dynamics in habitat quality and its effect on habitat selection by multiple cohorts of bluefish. Intra-annual recruitment to coastal areas of southern New Jersey was episodic, and resulted from the ingress of spring-spawned bluefish (hatch-date April) to estuarine beaches in late May to early June, followed by the recruitment of summer-spawned fish (hatch-date early July) to ocean beaches from July to October. Bluefish utilized estuarine and ocean beaches in a facultative manner that was responsive to dynamics in prey composition and temperature conditions. The recruitment and residency of bluefish in the estuary (1998–1999) and ocean beaches (1998), for example, was coincidental with the presence of the Atlantic silverside Menidia menidia and bay anchovy Anchoa mitchilli, the principal prey species for bluefish occupying these respective habitat-types. Bluefish abundance in the estuary (2000) and ocean beaches (1999–2000) was also correlated with water temperature, with the greatest catches of juveniles coinciding with their optimal growth temperature (24 °C). Bluefish growth, estimated as the slope of age–length relationships and daily specific growth rates, equaled 1.27–2.63 mm fork length (FL) d−1 and 3.8–8.7% body length increase d−1, respectively. The growth of sagittal otoliths was also used as a proxy for changes in bluefish size during and shortly before their time of capture. Accordingly, otolith growth rates of summer-spawned bluefish were greater at ocean beaches relative to the estuary and were explained by the more suitable temperature conditions found at ocean beaches during the mid- to late summer. Notwithstanding the fast growth of oceanic summer-spawned bluefish, individuals spawned in the spring were still larger in absolute body size at the end of the summer growing season (240 and 50–200 mm FL for spring- and summer-spawned bluefish, respectively). The size discrepancy between spring- and summer-spawned bluefish at the onset of autumn migrations and during overwintering periods may account for the differential recruitment success of the respective cohorts.  相似文献   
963.
We collected surface water along the 142nd E meridian from Tasmania to Antarctica in December 1999. We measured temperature, salinity and total chlorophyll a; additionally, we collected suspended particle size fractions and used fluorometric analysis to determine the quantity of chlorophyll a in each of four cell size classes: picoplankton (<3 μm), two nanoplankton fractions (3–10 μm and 10–20 μm) and microplankton (> 20 μm). Changes in temperature and salinity show that we crossed 6 water masses separated by 5 fronts. We found low abundance (<0.2 mg m−3) of chlorophyll in all size classes, with the exception of higher values near the continent (0.2 to 0.4 mg m−3). Lowest chlorophyll values (<0.1 mg m−3) were found in the Polar Frontal Zone (51° to 54°S). Microplankton made up the largest portion of total chlorophyll throughout most of the region. We conclude that biomass of all phytoplankton fractions, especially pico-and nanoplankton, was constrained by limiting factors, most probably iron, throughout the region and that ecosystem dynamics within a zone are not circumpolar but are regionalized within sectors.  相似文献   
964.
Iron chemistry in seawater has been extensively studied in the laboratory, mostly in small-volume sample bottles. However, little has been reported about iron wall sorption in these bottles. In this paper, radio-iron 55Fe was used to assess iron wall adsorption, both in terms of capacity, affinity and kinetics. Various bottle materials were tested. Iron sorption increased from polyethylene/polycarbonate to polymethylmetacrylate (PMMA)/high-density polyethylene/polytetrafluoroethylene to glass/quartz, reaching equilibrium in a 25–70 h period. PMMA was studied in more detail: ferric iron (Fe(III)) adsorbed on the walls of the bottles, whereas ferrous iron (Fe(II)) did not. Considering that in seawater the inorganic iron pool mostly consists of ferric iron, the wall will be a factor that needs to be considered in bottle experiments.The present data indicate that for PMMA with specific surface (S)-to-volume (V) ratio S/V, both iron capacity (42 ± 16 × 10− 9 mol/m2 or 1.7 × 10− 9 mol/L recalculated for the S/V-specific PMMA bottles used) and affinity (log KFe'W = 11.0 ± 0.3 m2/mol or 12.4 ± 0.3 L/mol, recalculated for the S/V-specific PMMA bottles used) are of similar magnitude as the iron capacity and -affinity of the natural ligands in the presently used seawater and thus cannot be ignored.Calculation of rate constants for association and dissociation of both Fe'L (iron bound to natural occurring organic ligands) and Fe'W (iron adsorbed on the wall of vessels) suggests that the two iron complexes are also of rather similar kinetics, with rate constants for dissociation in the order of 10 −4–10− 5 L/s and rate constants for association in the order of 108 L/(mol s). This makes that iron wall sorption should be seriously considered in small-volume experiments, both in assessments of shorter-term dynamics and in end-point observations in equilibrium conditions. Therefore, the present data strongly advocate making use of iron mass balances throughout in experiments in smaller volume set-ups on marine iron (bio) chemistry.  相似文献   
965.
A non-hydrostatic algorithm for the Regional Oceanic Modeling System (ROMS) is proposed. It is based on a decomposition technique for hydrostatic and non-hydrostatic pressure. The algorithm has a pressure-correction scheme with split-explicit time-stepping for baroclinic and barotropic vertical modes with a free surface. The algorithm implementation requires solving a Poisson equation for a non-hydrostatic pressure that has a non-symmetric matrix in discrete form. The efficiency of a different class of solvers and preconditioners were tested. The algorithm is successfully implemented with several examples where non-hydrostatic effects are important. These include standing external gravity waves; strongly nonlinear internal wave generation and transformation; stratified shear instability and its associated mixing; and nonlinear internal tidal generation over a ridge. The corresponding changes in the pre-processing and post-processing infrastructure in the existing hydrostatic ROMS code were performed to implement parallel elliptic solvers and a new set of dynamical equations.  相似文献   
966.
We describe the structure, reproductive cycle, fecundity, growth, and mortality of a harvested population of the ghost shrimp Callichirus major. Samples were collected at monthly intervals from September 1999 to October 2000 on an urban sandy beach (08°11′S 34°55′W) in northeastern Brazil. During this period the sex ratio did not differ significantly from 1:1 (0.98 M: 1 F). Minimum and maximum sizes of the Dorsal Oval were 2.59 and 12.19 mm for males and 4.46 and 12.62 mm for females, respectively. Ovigerous females were found throughout the period, except between August and September 2000. Maximum lifespan was estimated as 3.3 and 3.4 years for females and males, respectively. This northeastern population differed from others previously studied in southern and southeastern Brazil, in regard to sex ratio, maximum attained size, maturation size, period and duration of the reproductive cycle, and fecundity. We interpret these regional differences as evidence for over-fishing at the study site, and suggest that large-scale management plans for callianassid populations should use regional population parameters.  相似文献   
967.
We examined whether adults of three species of sea urchins species (Diadema antillarum, Arbacia lixula, and Paracentrotus lividus) exhibit a consistent depth-dependent partitioning pattern on rocky reefs of the Canarian Archipelago (eastern Atlantic). Hydrodynamic experiments were carried out to quantify the resistance to flow-induced dislodgement in these three species. We tested the model that different morphology can result in habitat partitioning among these sea urchins. Abundances of D. antillarum increased with depth. In contrast, A. lixula and P. lividus showed the opposite zonation pattern, coexisting in high abundances in the shallowest depths (<5 m), and occurring in low densities in the deepest part of reefs (>7 m). Both A. lixula and P. lividus had greater adhesion-surface to body-height ratios than D. antillarum. Similarly, A. lixula and P. lividus showed a greater ability to resist flow-induced dislodgement compared with D. antillarum. The mean “velocity of dislodgement” was 300% and 50% greater for A. lixula and P. lividus, respectively, relative to D. antillarum, for any particular size. As a result, A. lixula and P. lividus are better fitted to life in high-flow environments than D. antillarum. We conclude that the risk of dislodgement by water motion likely play a relevant role in the vertical distribution patterns of these sea urchins in the eastern Atlantic.  相似文献   
968.
根据1998年和2000年东海北部的营养盐调查资料和相应的历史资料,以及同期开展的虾类资源调查资料,研究了冬、夏季长江冲淡水的流向以及它对长江口渔场、舟山渔场硅酸盐分布规律和虾类生物量分布规律的影响。结果表明,长江冲淡水转向的原因可以归纳为4类,夏季长江冲淡水的流动界限由123°E,30.3°N到127.3°E,33°N的直线和由123°E,31.8°N到127.3°E,34.5°N的直线所围的区域。长江冲淡水给长江口渔场、舟山渔场提供了大量的硅酸盐,对提高该海区的初级生产力起到了积极的作用,有利于生物的繁衍生息,提高了生物量。最后,用该海区虾类的分布密度证实了由该水团所做出的对生物量的推论。  相似文献   
969.
于2007年5月至2010年5月间,在湄洲湾海域设置50个浅海测站,16条软相潮间带断面,进行底栖生物调查,根据调查采获的多毛类动物样品进行整理,研究湄洲湾多毛类物种多样性及生态特点.湄洲湾海域共鉴定有多毛类环节动物177种,隶属4l科112属.湄洲湾多毛类的动物区系特点与台湾海峡具有相似的热带、亚热带特征.讨论多毛类环节动物在调查区域底栖生物种类及数量组成中的地位,分析调查区域多毛类多样性指数等生态特征,为湄洲湾的生态环境监控、环境保护提供多毛类生态学的资料.  相似文献   
970.
In the present paper, a hydroelastic model is developed to deal with surface gravity wave interaction with an elastic bed based on the small amplitude water wave theory and plate deflection in finite water depth. The elastic bottom bed is modelled as a thin elastic plate and is based on the Euler-Bernoulli beam equation. The wave characteristics in the presence of the elastic bed is analyzed in both the cases of deep and shallow water waves. Further, the linearized long wave equation is generalized to include bottom flexibility. A generalized expansion formula for the velocity potential is derived to deal with the boundary value problems associated with surface gravity waves having an elastic bed. The utility of the expansion formula is illustrated by demonstrating specific physical problems which will play significant role in the analysis of wave structure interaction problems. Behavior of the wave spectra are discussed in the case of closed basin having a free surface and an elastic bottom topography.  相似文献   
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