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41.
Coral reefs throughout the world are under severe challenges from many environmental factors. This paper quantifies the size structure of populations and the growth rates of corals from 2000 to 2008 to test whether the Discovery Bay coral colonies showed resilience in the face of multiple acute stressors of hurricanes and bleaching. There was a reduction in numbers of colonies in the smallest size class for all the species at all the sites in 2006, after the mass bleaching of 2005, with subsequent increases for all species at all sites in 2007 and 2008. Radial growth rates (mm yr−1) of non-branching corals and linear extension rates (mm yr−1) of branching corals calculated on an annual basis from 2000–2008 showed few significant differences either spatially or temporally. At Dairy Bull reef, live coral cover increased from 13 ± 5% in 2006 to 20 ± 9% in 2007 and 31 ± 7% in 2008, while live Acropora species increased from 2 ± 2% in 2006 to 10 ± 4% in 2007 and 22 ± 7% in 2008. These studies indicate good levels of coral resilience on the fringing reefs around Discovery Bay in Jamaica.  相似文献   
42.
Since the early 1980s, episodes of coral reef bleaching and mortality, due primarily to climate-induced ocean warming, have occurred almost annually in one or more of the world's tropical or subtropical seas. Bleaching is episodic, with the most severe events typically accompanying coupled ocean–atmosphere phenomena, such as the El Niño-Southern Oscillation (ENSO), which result in sustained regional elevations of ocean temperature. Using this extended dataset (25+ years), we review the short- and long-term ecological impacts of coral bleaching on reef ecosystems, and quantitatively synthesize recovery data worldwide. Bleaching episodes have resulted in catastrophic loss of coral cover in some locations, and have changed coral community structure in many others, with a potentially critical influence on the maintenance of biodiversity in the marine tropics. Bleaching has also set the stage for other declines in reef health, such as increases in coral diseases, the breakdown of reef framework by bioeroders, and the loss of critical habitat for associated reef fishes and other biota. Secondary ecological effects, such as the concentration of predators on remnant surviving coral populations, have also accelerated the pace of decline in some areas. Although bleaching severity and recovery have been variable across all spatial scales, some reefs have experienced relatively rapid recovery from severe bleaching impacts. There has been a significant overall recovery of coral cover in the Indian Ocean, where many reefs were devastated by a single large bleaching event in 1998. In contrast, coral cover on western Atlantic reefs has generally continued to decline in response to multiple smaller bleaching events and a diverse set of chronic secondary stressors. No clear trends are apparent in the eastern Pacific, the central-southern-western Pacific or the Arabian Gulf, where some reefs are recovering and others are not. The majority of survivors and new recruits on regenerating and recovering coral reefs have originated from broadcast spawning taxa with a potential for asexual growth, relatively long distance dispersal, successful settlement, rapid growth and a capacity for framework construction. Whether or not affected reefs can continue to function as before will depend on: (1) how much coral cover is lost, and which species are locally extirpated; (2) the ability of remnant and recovering coral communities to adapt or acclimatize to higher temperatures and other climatic factors such as reductions in aragonite saturation state; (3) the changing balance between reef accumulation and bioerosion; and (4) our ability to maintain ecosystem resilience by restoring healthy levels of herbivory, macroalgal cover, and coral recruitment. Bleaching disturbances are likely to become a chronic stress in many reef areas in the coming decades, and coral communities, if they cannot recover quickly enough, are likely to be reduced to their most hardy or adaptable constituents. Some degraded reefs may already be approaching this ecological asymptote, although to date there have not been any global extinctions of individual coral species as a result of bleaching events. Since human populations inhabiting tropical coastal areas derive great value from coral reefs, the degradation of these ecosystems as a result of coral bleaching and its associated impacts is of considerable societal, as well as biological concern. Coral reef conservation strategies now recognize climate change as a principal threat, and are engaged in efforts to allocate conservation activity according to geographic-, taxonomic-, and habitat-specific priorities to maximize coral reef survival. Efforts to forecast and monitor bleaching, involving both remote sensed observations and coupled ocean–atmosphere climate models, are also underway. In addition to these efforts, attempts to minimize and mitigate bleaching impacts on reefs are immediately required. If significant reductions in greenhouse gas emissions can be achieved within the next two to three decades, maximizing coral survivorship during this time may be critical to ensuring healthy reefs can recover in the long term.  相似文献   
43.
Recent findings on water masses, biogeochemical tracers, deep currents and basin-scale circulation in the East/Japan Sea, and numerical modeling of its circulation are reviewed. Warming continues up to 2007 despite an episode of bottom water formation in the winter of 2000–2001. Water masses have definitely changed since the 1970s and further changes are expected due to the continuation of warming. Accumulation of current data in deep waters of the East/Japan Sea reveals that the circulation in the East/Japan Sea is primarily cyclonic with sub-basin scale cyclonic and anticyclonic cells in the Ulleung Basin (Tsushima Basin). Our understanding of the circulation of intermediate water masses has been deepened through high-resolution numerical studies, and the implementation of data assimilation has had initial success. However, the East/Japan Sea is unique in terms of the fine vertical structures of physical and biogeochemical properties of cold water mass measured at the highest precision and their rapid change with the global warming, so that full understanding of the structures and their change requires in-depth process studies with continuous monitoring programs.  相似文献   
44.
海洋浮游动物多样性及其分布对全球变暖的响应   总被引:1,自引:0,他引:1  
针对日益加剧的全球增温和生物多样性丧失等现象,结合浮游动物在海洋生态系统中的重要性,从世界各大海域的浮游甲壳类、水母类及毛颚类等群落对海洋表层温度升高及海流变化的响应等方面进行了综述,以期为进一步深入开展相关研究提供参考。  相似文献   
45.
46.
This study investigates the Arctic Ocean warming episodes in the 20th century using both a high-resolution coupled global climate model and historical observations. The model, with no flux adjustment, reproduces well the Atlantic Water core temperature (AWCT) in the Arctic Ocean and shows that four largest decadalscale warming episodes occurred in the 1930s, 70s, 80s, and 90s, in agreement with the hydrographic observational data. The difference is that there was no pre-warming prior to the 1930s episode, while there were two pre-warming episodes in the 1970s and 80s prior to the 1990s, leading the 1990s into the largest and prolonged warming in the 20th century. Over the last century, the simulated heat transport via Fram Strait and the Barents Sea was estimated to be, on average, 31.32 TW and 14.82 TW, respectively, while the Bering Strait also provides 15.94 TW heat into the west- ern Arctic Ocean. Heat transport into the Arctic Ocean by the Atlantic Water via Fram Strait and the Barents Sea correlates significantly with AWCT ( C = 0.75 ) at 0- lag. The modeled North Atlantic Oscillation (NAO) index has a significant correlation with the heat transport ( C = 0.37 ). The observed AWCT has a significant correlation with both the modeled AWCT ( C =0.49) and the heat transport ( C =0.41 ). However, the modeled NAO index does not significantly correlate with either the observed AWCT ( C = 0.03 ) or modeled AWCT ( C = 0.16 ) at a zero-lag, indicating that the Arctic climate system is far more complex than expected.  相似文献   
47.
过去的几个冬季中,北美、欧洲、西伯利亚和东亚大部分地区经历了冷冬和强降雪,而这与北极海冰的快速减少有关。尽管北极海冰减少在冷冬和强降雪中的作用仍存在争议,但这种新兴的气候反馈在未来变暖背景下是否会持续仍值得关注。中等排放情境下的气候模式模拟结果揭示,欧洲东北部、亚洲中部北部、北美北部的冬季降雪增加会成为贯穿21世纪的一个稳健的特征。21世纪这些区域冬季降雪增加的主要原因是北极秋季海冰的减少(很大的外部强迫),而冬季北极涛动的变化(北半球主要的自然变化形态)对降雪增加的作用很小。这一结果不仅体现在多模式平均上,而且每个单独模式的结果依然如此。我们认为海冰-降雪之间的强反馈作用可能已经出现,并且在接下来的几十年中这种强反馈作用可能会增强,北半球高纬地区的强降雪事件也会增加。  相似文献   
48.
本文系统梳理了IPCC 《气候变化中的海洋和冰冻圈特别报告》(SROCC)的主要结论,并对主要观点进行了解读。报告主要关注全球变暖背景下高山、极地、海洋和沿海地区现在和未来的变化及其对人类和生态系统的影响,以及实现气候适应发展路径的方案。在全球变暖背景下,冰冻圈大面积萎缩,冰川冰盖质量损失,积雪减少,北极海冰范围和厚度减小,多年冻土升温,全球海洋持续增温,1993年以来,海洋变暖和吸热速度增加了一倍以上。同时,海洋表面酸化加剧,海洋含氧量减少。全球平均海平面呈加速上升趋势,2006—2015年全球海平面上升速率为3.6 mm/yr,是1901—1990年的2.5倍,但存在区域差异。高山、极地和海洋的生态系统的物种组成、分布和服务功能均发生变化,并对人类社会产生了显著负面影响。极端海洋气候事件发生频率增多,强度加大。1982年以来,全球范围内海洋热浪的发生频率增加了一倍,且范围更广,持续时间更长。海平面持续上升加剧了洪涝、海水入侵、海岸侵蚀等海岸带灾害,并影响沿海生态系统。海洋及冰冻圈的变化及其影响在未来一定时期仍将持续,应对这些影响而面临的挑战,应加强基于生态系统的适应和可再生能源管理,强化海岸带地区的海平面上升综合应对,打造积极有效、可持续和具有韧性的气候变化应对方案。  相似文献   
49.
Brief Review of Some CLIVAR-Related Studies in China   总被引:2,自引:0,他引:2  
The Climate Variability and Predictability (CLIVAR) program is one of the sub-programs of the World Climate Research Program (WCRP). In this paper, CLIVAR related research in China (2003-2006) is briefly reviewed, including four major components, namely, low-frequency intraseasonal oscillations, interannual variability, decadal variations in East Asia, and global warming simulations.  相似文献   
50.
There are serious concerns that ocean acidification will combine with the effects of global warming to cause major shifts in marine ecosystems, but there is a lack of field data on the combined ecological effects of these changes due to the difficulty of creating large‐scale, long‐term exposures to elevated CO2 and temperature. Here we report the first coastal transplant experiment designed to investigate the effects of naturally acidified seawater on the rates of net calcification and dissolution of the branched calcitic bryozoan Myriapora truncata (Pallas, 1766). Colonies were transplanted to normal (pH 8.1), high (mean pH 7.66, minimum value 7.33) and extremely high CO2 conditions (mean pH 7.43, minimum value 6.83) at gas vents off Ischia Island (Tyrrhenian Sea, Italy). The net calcification rates of live colonies and the dissolution rates of dead colonies were estimated by weighing after 45 days (May–June 2008) and after 128 days (July–October) to examine the hypothesis that high CO2 levels affect bryozoan growth and survival differently during moderate and warm water conditions. In the first observation period, seawater temperatures ranged from 19 to 24 °C; dead M. truncata colonies dissolved at high CO2 levels (pH 7.66), whereas live specimens maintained the same net calcification rate as those growing at normal pH. In extremely high CO2 conditions (mean pH 7.43), the live bryozoans calcified significantly less than those at normal pH. Therefore, established colonies of M. truncata seem well able to withstand the levels of ocean acidification predicted in the next 200 years, possibly because the soft tissues protect the skeleton from an external decrease in pH. However, during the second period of observation a prolonged period of high seawater temperatures (25–28 °C) halted calcification both in controls and at high CO2, and all transplants died when high temperatures were combined with extremely high CO2 levels. Clearly, attempts to predict the future response of organisms to ocean acidification need to consider the effects of concurrent changes such as the Mediterranean trend for increased summer temperatures in surface waters. Although M. truncata was resilient to short‐term exposure to high levels of ocean acidification at normal temperatures, our field transplants showed that its ability to calcify at higher temperatures was compromised, adding it to the growing list of species now potentially threatened by global warming.  相似文献   
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