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臭氧活性炭工艺中卤乙酸生成潜能与相对分子质量分布关系的研究 总被引:4,自引:0,他引:4
通过臭氧生物活性炭和微曝气生物活性炭(O3/BAC和micro-aeration/BAC)2套工艺研究其对不同相对分子质量有机物去除特点和不同相对分子量有机物生成的卤乙酸及其去除特性.结果表明,O3/BAC工艺对相对分子质量区间>30×103的有机物去除率超过90%.O3/BAC与micro-aeration/BAC出水中,UV254值表示相对分子质量<103的有机物超过50%,相对分子量区间在10×103~30×103的有机物占20%~30%;在O3/BAC和微曝气/BAC工艺出水中,以相对分子质量<103的有机物生成的卤乙酸最多,生成DCAA、TCAA、DBAA分别为97.00、38.55、2.10μg/L和104.00、42.75和2.92μg/L;采用各处理单元不同分子量有机物与氯反应生成的DCAA、TCAA、DBAA和THAAs与相对应的UV254值进行线性拟合,相关系数分别为0.827、0.851 3、0.815 7和0.878.UV254与臭氧生物活性炭处理工艺出水中的卤乙酸生成潜能具有较好的线性关系. 相似文献
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以煤矸石为原料,采用碱熔-水热法合成4A沸石分子筛。由于煤矸石中铝、硅主要以高岭土形式存在,其活化过程是合成4A沸石分子筛关键环节。为提高4A沸石分子筛钙离子的交换能力,增加对模拟废水氨氮的去除率,实验考察了碳酸钠与煤矸石质量比、活化温度、活化时间、晶化温度和晶化时间对4A沸石分子筛钙离子交换能力的影响,同时也考察了模拟废水的pH、4A沸石分子筛加入量及吸附时间对氨氮去除率的影响。结果表明,最佳工艺条件为,碳酸钠与煤矸石质量比为0.9、活化温度为800℃、活化时间1.5 h、晶化温度90℃和晶化时间3 h。合成4A沸石分子筛的钙离子交换能力为310 mg/g,在pH为6的100 mL模拟氨氮废水中加入6 g 4A沸石分子筛吸附40 min后,废水中氨氮的去除率达到86%。通过最佳工艺条件合成4A沸石分子筛,在处理氨氮废水方面具有一定的应用前景。 相似文献
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表面活性剂改性4A分子筛对Cr(VI)的吸附行为 总被引:1,自引:0,他引:1
采用浸渍法对4A分子筛进行表面改性,通过引入阳离子表面活性剂,使4A分子筛表面附着季铵型阳离子,并与反离子Br-形成"阴离子交换膜",从而促使更多的Cr(VI)阴离子通过离子交换吸附到改性4A分子筛上,通过X-射线衍射(XRD)和傅里叶变换红外光谱(FTIR)对样品的物相结构和组成进行表征分析。研究表明,表面活性剂的类型和疏水碳氢链结构会影响4A分子筛的吸附能力,十八烷基三甲基溴化铵(OTAB)碳氢链长,在分子筛表面形成的双分子层密,对Cr(VI)的吸附量最大。采用准一级、准二级、Elovich和Bangham动力学模型对六价铬的吸附数据进行拟合,其中准一级动力学方程最符合十八烷基三甲基溴化铵改性分子筛的吸附行为。同时,分别从Langmuir和Redlich-Peterson等温吸附模型获得六价铬的最大吸附量为13.98 mg/g,且改性分子筛以均一表面吸附为主。 相似文献
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Pasan Samarasin Brian J. Shuter Stephen I. Wright F. Helen Rodd 《Conservation biology》2017,31(1):126-135
Accurate understanding of population connectivity is important to conservation because dispersal can play an important role in population dynamics, microevolution, and assessments of extirpation risk and population rescue. Genetic methods are increasingly used to infer population connectivity because advances in technology have made them more advantageous (e.g., cost effective) relative to ecological methods. Given the reductions in wildlife population connectivity since the Industrial Revolution and more recent drastic reductions from habitat loss, it is important to know the accuracy of and biases in genetic connectivity estimators when connectivity has declined recently. Using simulated data, we investigated the accuracy and bias of 2 common estimators of migration (movement of individuals among populations) rate. We focused on the timing of the connectivity change and the magnitude of that change on the estimates of migration by using a coalescent‐based method (Migrate‐n) and a disequilibrium‐based method (BayesAss). Contrary to expectations, when historically high connectivity had declined recently: (i) both methods over‐estimated recent migration rates; (ii) the coalescent‐based method (Migrate‐n) provided better estimates of recent migration rate than the disequilibrium‐based method (BayesAss); (iii) the coalescent‐based method did not accurately reflect long‐term genetic connectivity. Overall, our results highlight the problems with comparing coalescent and disequilibrium estimates to make inferences about the effects of recent landscape change on genetic connectivity among populations. We found that contrasting these 2 estimates to make inferences about genetic‐connectivity changes over time could lead to inaccurate conclusions. 相似文献
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STEPHANIE S. COSTER JESSICA S. VEYSEY POWELL KIMBERLY J. BABBITT 《Conservation biology》2014,28(3):756-762
Habitat linkages can help maintain connectivity of animal populations in developed landscapes. However, the lack of empirical data on the width of lateral movements (i.e., the zigzagging of individuals as they move from one point to point another) makes determining the width of such linkages challenging. We used radiotracking data from wood frogs (Lithobates sylvaticus) and spotted salamanders (Ambystoma maculatum) in a managed forest in Maine (U.S.A.) to characterize movement patterns of populations and thus inform planning for the width of wildlife corridors. For each individual, we calculated the polar coordinates of all locations, estimated the vector sum of the polar coordinates, and measured the distance from each location to the vector sum. By fitting a Gaussian distribution over a histogram of these distances, we created a population‐level probability density function and estimated the 50th and 95th percentiles to determine the width of lateral movement as individuals progressed from the pond to upland habitat. For spotted salamanders 50% of lateral movements were ≤13 m wide and 95% of movements were ≤39 m wide. For wood frogs, 50% of lateral movements were ≤17 m wide and 95% of movements were ≤ 51 m wide. For both species, those individuals that traveled the farthest from the pond also displayed the greatest lateral movement. Our results serve as a foundation for spatially explicit conservation planning for pond‐breeding amphibians in areas undergoing development. Our technique can also be applied to movement data from other taxa to aid in designing habitat linkages. Caracterización de la Amplitud de Movimiento de Anfibios durante la Migración Pos‐Reproducción 相似文献
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NICK M. HADDAD LARS A. BRUDVIG ELLEN I. DAMSCHEN DANIEL M. EVANS BRENDA L. JOHNSON DOUGLAS J. LEVEY JOHN L. ORROCK JULIAN RESASCO LAUREN L. SULLIVAN JOSH J. TEWKSBURY STEPHANIE A. WAGNER AIMEE J. WELDON 《Conservation biology》2014,28(5):1178-1187
Despite many studies showing that landscape corridors increase dispersal and species richness for disparate taxa, concerns persist that corridors can have unintended negative effects. In particular, some of the same mechanisms that underlie positive effects of corridors on species of conservation interest may also increase the spread and impact of antagonistic species (e.g., predators and pathogens), foster negative effects of edges, increase invasion by exotic species, increase the spread of unwanted disturbances such as fire, or increase population synchrony and thus reduce persistence. We conducted a literature review and meta‐analysis to evaluate the prevalence of each of these negative effects. We found no evidence that corridors increase unwanted disturbance or non‐native species invasion; however, these have not been well‐studied concerns (1 and 6 studies, respectively). Other effects of corridors were more often studied and yielded inconsistent results; mean effect sizes were indistinguishable from zero. The effect of edges on abundances of target species was as likely to be positive as negative. Corridors were as likely to have no effect on antagonists or population synchrony as they were to increase those negative effects. We found 3 deficiencies in the literature. First, despite studies on how corridors affect predators, there are few studies of related consequences for prey population size and persistence. Second, properly designed studies of negative corridor effects are needed in natural corridors at scales larger than those achievable in experimental systems. Third, studies are needed to test more targeted hypotheses about when corridor‐mediated effects on invasive species or disturbance may be negative for species of management concern. Overall, we found no overarching support for concerns that construction and maintenance of habitat corridors may result in unintended negative consequences. Negative edge effects may be mitigated by widening corridors or softening edges between corridors and the matrix. Other negative effects are relatively small and manageable compared with the large positive effects of facilitating dispersal and increasing diversity of native species. Efectos Negativos Potenciales de los Corredores 相似文献