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171.
In planktonic food webs, the conversion rate of plant material to herbivore biomass is determined by a variety of factors such as seston biochemical/elemental composition, phytoplankton cell morphology, and colony architecture. Despite the overwhelming heterogeneity characterizing the plant–animal interface, plankton population models usually misrepresent the food quality constraints imposed on zooplankton growth. In this study, we reformulate the zooplankton grazing term to include seston food quality effects on zooplankton assimilation efficiency and examine its ramifications on system stability. Using different phytoplankton parameterizations with regards to growth strategies, light requirements, sinking rates, and food quality, we examined the dynamics induced in planktonic systems under varying zooplankton mortality/fish predation, light conditions, nutrient availability, and detritus food quality levels. In general, our analysis suggests that high food quality tends to stabilize the planktonic systems, whereas unforced oscillations (limit cycles) emerge with lower seston food quality. For a given phytoplankton specification and resource availability, the amplitude of the plankton oscillations is primarily modulated from zooplankton mortality and secondarily from the nutritional quality of the alternative food source (i.e., detritus). When the phytoplankton community is parameterized as a cyanobacterium-like species, conditions of high nutrient availability combined with high zooplankton mortality led to phytoplankton biomass accumulation, whereas a diatom-like parameterization resulted in relatively low phytoplankton to zooplankton biomass ratios highlighting the notion that high phytoplankton food quality allows the zooplankton community to sustain relatively high biomass and to suppress phytoplankton biomass to low levels. During nutrient and light enrichment conditions, both phytoplankton and detritus food quality determine the extent of the limit cycle region, whereas high algal food quality increases system resilience by shifting the oscillatory region towards lower light attenuation levels. Detritus food quality seems to regulate the amplitude of the dynamic oscillations following enrichment, when algal food quality is low. These results highlight the profitability of the alternative food sources for the grazer as an important predictor for the dynamic behavior of primary producer–grazer interactions in nature.  相似文献   
172.
In the present paper we propose a modification of a basic eco-epidemiological model by incorporating predator switching among susceptible and infected prey population. A local and global study of the basic model is performed around the disease-free boundary equilibrium and the interior equilibrium to estimate important parameter thresholds that control disease eradication and species coexistence. Next we analyze the switching model from the same perspective in order to elucidate the role of switching on disease dynamics. Numerical simulations are carried out to justify analytical results.  相似文献   
173.
EcoTroph (ET) is a model articulated around the idea that the functioning of aquatic ecosystems may be viewed as a biomass flow moving from lower to higher trophic levels, due to predation and ontogenetic processes. Thus, we show that the ecosystem biomass present at a given trophic level may be estimated from two simple equations, one describing biomass flow, the other their kinetics (which quantifies the velocity of biomass transfers towards top predators). The flow kinetic of prey partly depends on the abundance of their predators, and a top-down equation expressing this is included in the model. Based on these relationships, we simulated the impact on a virtual ecosystem of various exploitation patterns. Specifically, we show that the EcoTroph approach is able to mimic the effects of increased fishing effort on ecosystem biomass expected from theory. Particularly, the model exhibits complex patterns observed in field data, notably cascading effects and ‘fishing down the food web’. EcoTroph also provides diagnostic tools for examining the relationships between catch and fishing effort at the ecosystem scale and the effects of strong top-down controls and fast-flow kinetics on ecosystems resilience. Finally, a dynamic version of the model is derived from the steady-state version, thus allowing simulations of time series of ecosystem biomass and catches. Using this dynamic model, we explore the propagation of environmental variability in the food web, and illustrated how exploitation can induce a decrease of ecosystem stability. The potential for applying EcoTroph to specific ecosystems, based on field data, and similarities between EcoTroph and Ecopath with Ecosim (EwE) are finally discussed.  相似文献   
174.
讨论了无量纲廓线函数对稳定度分类标准计算结果的影响,利用北京325m气象铁塔的超声脉动资料和常规梯度观测资料,对4种无量纲廓线函数进行比较.结果表明,对于北京地区Businger-Hick公式最合适,风速比法稳定度分类标准不是稳定度级别的单调函数.  相似文献   
175.
ABSTRACT: Stream channels are known to change their form as a result of watershed urbanization, but do they restabilize under subsequent conditions of constant urban land use? Streams in seven developed and developing watersheds (drainage areas 5–35 km2) in the Puget Sound lowlands were evaluated for their channel stability and degree of urbanization, using field and historical data. Protocols for determining channel stability by visual assessment, calculated bed mobility at bankfull flows, and resurveyed cross‐sections were compared and yielded nearly identical results. We found that channel restabilization generally does occur within one or two decades of constant watershed land use, but it is not universal. When (or if) an individual stream will restabilize depends on specific hydrologic and geomorphic characteristics of the channel and its watershed; observed stability is not well predicted by simply the magnitude of urban development or the rate of ongoing land‐use change. The tendency for channel restabilization suggests that management efforts focused primarily on maintaining stability, particularly in a still‐urbanizing watershed, may not always be necessary. Yet physical stability alone is not a sufficient condition for a biologically healthy stream, and additional rehabilitation measures will almost certainly be required to restore biological conditions in urban systems.  相似文献   
176.
提供生物稳定饮用水的最佳工艺   总被引:20,自引:1,他引:19  
研究由预处理、常规处理和深度处理组合而成的 7种不同工艺对饮用水源水中可生物同化有机碳 ( AOC)的去除效果 .试验表明 :生物陶粒预处理对 AOC具有较高的去除率 ,达到 45%左右 ,如果在它之前先经过预臭氧化 ,生物处理的去除率可增大到 58.4% ;常规处理对 AOC的去除非常有限 ,去除率平均在 2 0 %左右 ;新活性炭单元因其吸附作用对 AOC的去除效果稳定在30 %左右 ,如和臭氧氧化连用 ,去除效果能提高到 50 %以上 ;包括了常规处理、生物预处理、预臭氧和臭氧活性炭的组合工艺对AOC的去除效果最好 ,达到 86% .因此臭氧氧化、生物炭和生物处理是提高饮用水生物稳定性的重要手段 ,并以本试验结果为依据提出了对于不同的水源水所采用的最佳工艺 .  相似文献   
177.
我国生态工业系统稳定性的结构型因素实证研究   总被引:8,自引:0,他引:8  
在查阅国内外大量文献的基础上,提出了5个可能影响我国生态工业系统稳定性的结构型因素假设:关键种企业、成员距离、成员相互依赖程度、成员多样性、领导因素.并在全国47个生态工业系统进行统计实证研究加以证实.数据相关分析和回归分析结果表明:强有力的系统内部关键种企业、较少的成员交流障碍、较近的成员空间距离、多样化的成员企业主营业务等4个因素对我国生态工业系统稳定性有显著影响.对我国生态工业系统的发展提出了相应的政府决策建议.   相似文献   
178.
净水工艺对饮用水生物稳定性控制的研究   总被引:1,自引:1,他引:0  
利用现场中试装置,系统比较了预处理单元、常规处理单元及深度处理单元中可生物降解有机物BDOC和AOC的生成和去除特性.结果表明:常规工艺+活性炭过滤对CODMn的去除率仅能达到30%,无法有效保证出水水质要求,而常规工艺+臭氧活性炭可以很好地满足水质标准,去除率可达50%以上.以控制生物稳定性为目的时,氧化剂的投加会增加AOC和BDOC浓度,降低生物稳定性.不投加氧化剂,直接采用常规工艺+普通活性炭过滤可将出水AOC含量控制在50μg/L以下.但要实现对CODMn和生物稳定性的同时控制,常规工艺+臭氧+生物活性炭的工艺组合是本研究中的最佳工艺组合.  相似文献   
179.
快速木质纤维素分解菌复合系MC1对秸秆的分解能力及稳定性   总被引:19,自引:2,他引:17  
以天然水稻秸秆为材料研究了快速降解木质纤维素的细菌复合系MC1对木质纤维素的分解能力;并在不同条件保藏、高温处理以及利用变性梯度胶电泳(DGGE)技术研究了复合系的稳定性.结果表明,复合系MC1在50℃液体静止培养条件下8~10d,把培养液2%干重的水稻秸秆完全分解溶化;经过9d的培养,水稻秸秆的总干重减少81%,其中纤维素减少99%,半纤维素减少74%,木质素减少51%.连续继代培养4a、常温干燥保存4a、-20℃冷冻藏4a、培养液直接在室温和4℃保存1a、90℃处理30min仍具旺盛的分解能力并稳定传代.平板培养基培养证明MC1全部由细菌组成,16SrDNA变性梯度胶电泳(DGGE)检测结果,在6个月内主要条带几乎没有变化,说明MC1的菌种组成相当稳定.MC1对纤维素的分解利用具重要前景.  相似文献   
180.
砷酸钙化合物的溶解度及其稳定性随pH值的变化   总被引:8,自引:0,他引:8  
通过混合沉淀和溶解实验详细研究了pH值和Ca/As摩尔比对石灰沉淀法处理高浓度含砷废水的影响.沉淀后溶液中的As浓度随pH值的变化趋势与混合液的Ca/As摩尔比有关,在Ca/As=1·50和1·67时,沉淀后溶液中的As浓度在pH=7附近达到最低,然后随pH值的升高而呈现出增大的趋势;在Ca/As=2·00和4·00时,沉淀后溶液中的As浓度随pH值的升高而降低,且2种Ca/As摩尔比条件下的实验结果基本一致.混合沉淀过程中生成的砷酸钙化合物的组成与结构取决于溶液的Ca/As摩尔比和pH值.在低pH值和低Ca/As摩尔比条件下形成的沉淀物要比在高pH值和高Ca/As摩尔比条件下形成的沉淀物的颗粒要大,而且结晶程度要好.在Ca/As摩尔比为1·0~4·0和不同pH值条件下,主要生成Ca_3(AsO_4)_2·3H_2O、Ca_3(AsO_4)_2·2·25H_2O、Ca_5(AsO-4)_3OH和Ca_4(OH)-2(AsO_4)2·4H_2O,溶度积分别等于10~(-21·14)、10~(-21·40)、10~(-40·12)和10~(-27·49).  相似文献   
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