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Louis W. Botsford Cathryn A. Lawrence Edward P. Dever Alan Hastings John Largier 《Deep Sea Research Part II: Topical Studies in Oceanography》2006,53(25-26):3116
The production and distribution of biological material in wind-driven coastal upwelling systems are of global importance, yet they remain poorly understood. Production is frequently presumed to be proportional to upwelling rate, yet high winds can lead to advective losses from continental shelves, where many species at higher trophic levels reside. An idealized mixed-layer conveyor (MLC) model of biological production from constant upwelling winds demonstrated previously that the amount of new production available to shelf species increased with upwelling at low winds, but declined at high winds [Botsford, L.W., Lawrence, C.A., Dever, E.P., Hastings, A., Largier, J., 2003. Wind strength and biological productivity in upwelling systems: an idealized study. Fisheries Oceanography 12, 245–259]. Here we analyze the response of this model to time-varying winds for parameter values and observed winds from the Wind Events and Shelf Transport (WEST) study region. We compare this response to the conventional view that the results of upwelling are proportional to upwelled volume. Most new production per volume upwelled available to shelf species occurs following rapid increases in shelf transit time due to decreases in wind (i.e. relaxations). However, on synoptic, event time-scales shelf production is positively correlated with upwelling rate. This is primarily due to the effect of synchronous periods of low values in these time series, paradoxically due to wind relaxations. On inter-annual time-scales, computing model production from wind forcing from 20 previous years shows that these synchronous periods of low values have little effect on correlations between upwelling and production. Comparison of model production from 20 years of wind data over a range of shelf widths shows that upwelling rate will predict biological production well only in locations where cross-shelf transit times are greater than the time required for phytoplankton or zooplankton production. For stronger mean winds (narrower shelves), annual production falls below the peak of constant wind prediction [Botsford et al., 2003. Wind strength and biological productivity in upwelling systems: an idealized study. Fisheries Oceanography 12, 245–259], then as winds increase further (shelves become narrower) production does not decline as steeply as the constant wind prediction. 相似文献
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本文综述了国内外关于介核生物(主要包括甲藻和裸藻)分子生物学方面的研究进展。介绍了介核生物的分子分类进展及其特殊的分类地位,甲藻毒素和裸藻在环境检测上的应用,同时简介了介核藻类活性物质的开发利用前景。 相似文献
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Viability theory for an ecosystem approach to fisheries 总被引:1,自引:1,他引:1
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In this paper, we focus on the status and trends of the current Korean fisheries management regime. Specifically, this paper briefly introduces the Korean conventional fisheries management regime (KCFMR) and discusses its problems and limitations. In describing policy evolution, this paper finds reasons why the Korean government has chosen a TAC system, an output control approach, besides input control approaches in force for almost a century. This paper also describes the evolution of the Korean TAC system, which is carrying out a pivotal role in Korean fisheries development, and analyzes problems of the Korean TAC system. Finally, this paper gives a perspective on expanding the Korean TAC system toward Output Control Systems (OCSs) such as Individual Quotas (IQs), Individual Vessel Quotas (IVQs), Individual Transferable Traps (ITTs), Community Quotas (CQs), and Individual Transferable Quotas (ITQs). 相似文献
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Abstract. Routine monthly samples of the commercially important portunid crab Liocarcimtx puber and the sympatric but ecologically separated L. holsatus were collected from the waters and shores around the Gowcr Peninsula, South Wales, between November 1983 and September 1985.
The pubertal moult in L. puber occurred at 38 mm CW (carapace width) (females) and 42 mm CW (males). In L. holsatus this occurred at 17 mm (females) and 18.5 mm CW (males). The median size of ovigcrous females was 49.2 ± 6.7 mm CW in L. puber and 26.5 ± 2.0 mm CW in L. holsatus.
Moulting and copulation occurred between spring and autumn, the moulting period of males being earlier than that of the females. Ovigcrous L. holsatus were recorded throughout the year, with highest proportions between February and April. L. puber were ovigcrous mainly between January and March; none was recorded between September and November. The number of eggs of the wild brood (range: 39,000–280,000 for L. holsatus and 40.000–262.000 for L. puber ) was related to female body size as y = 3.099.51 c0.1126x , r = 0.90, n = 21 and y = 6,335.98 c0.051x , r = 0.88, n = 23, respectively, where y = number of eggs and x = carapace width (mm).
Following successful copulation, females of both species were able to spawn more than once during an intcrmoult period. 相似文献
The pubertal moult in L. puber occurred at 38 mm CW (carapace width) (females) and 42 mm CW (males). In L. holsatus this occurred at 17 mm (females) and 18.5 mm CW (males). The median size of ovigcrous females was 49.2 ± 6.7 mm CW in L. puber and 26.5 ± 2.0 mm CW in L. holsatus.
Moulting and copulation occurred between spring and autumn, the moulting period of males being earlier than that of the females. Ovigcrous L. holsatus were recorded throughout the year, with highest proportions between February and April. L. puber were ovigcrous mainly between January and March; none was recorded between September and November. The number of eggs of the wild brood (range: 39,000–280,000 for L. holsatus and 40.000–262.000 for L. puber ) was related to female body size as y = 3.099.51 c
Following successful copulation, females of both species were able to spawn more than once during an intcrmoult period. 相似文献