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We examined arsenic (As) uptake by vegetable crops (amaranth, Amaranthus gangeticus, and silverbeet, Beta vulgaris) as affected by As speciation (AsIII and AsV) and their concentrations in nutrient solution. Amaranth and silverbeet were grown in a nutrient solution containing four levels of arsenate (AsV): 0, 1, 5, and 25 mg As/l and three levels of arsenite (AsIII): 0, 5, 10 mg As/l. Both AsV and AsIII are phytotoxic to these crops with the latter being five times more toxic. Amaranth treated with AsIII exhibited As toxicity symptoms within 48 h of exposure and was close to death within 1 week. However, AsV treatment did not show clear toxicity symptoms other than wilting and yield reduction at the highest dose rate of 25 mg AsV/l. The main mechanism used by vegetable crops to tolerate AsV is probably avoidance—limiting As transport to shoots and increasing As accumulation in the root system. When AsV was added to the nutrient solution, the uptake of As in shoots increased and, at the highest dose (25 mg AsV/l), 60 μg As/g DW (3.6 mg/kg FW) accumulated in the edible portion, which exceeds the WHO recommended limit for food stuffs (2 mg/kg FW) as the water contents of the crops were 94%. It is therefore important to determine the nature of the As species and their bio-accessibility. Iron treatment with 0.5 mg NaFe(III)EDTA/l dose decreased silverbeet As uptake by 45% given its affinity to bind As at the root surface or root rhizosphere and so restrict As translocation to the shoots.  相似文献   
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Pacific hake [Merluccius productus (Ayres)], migrating northward along the California coastline during summer, encounter the southwesterly flowing plume of the Columbia River. Radioactive 65Zn associated with the plume waters is taken up by the migrating hake. Smaller fish reflect this contamination earlier than larger fish. Zinc-65 specific activities increase toward the north as far as 46°N, off the mouth of the Columbia River, and then decline northward along the coast of Washington.  相似文献   
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Environmental Geochemistry and Health - Human health risk assessment at hydrocarbon-contaminated sites requires a critical evaluation of the exposure pathways of volatile organic compounds...  相似文献   
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The bioavailability of arsenic (As) in the soil environment is largely governed by its adsorption–desorption reactions with soil constituents. We have investigated the sorption–desorption behaviour of As in four typical Bangladeshi soils subjected to irrigation with As-contaminated groundwater. The total As content of soils (160 samples) from the Laksham district ranged from <0.03 to approximately 43 mg kg−1. Despite the low total soil As content, the concentration of As in the pore water of soils freshly irrigated with As-contaminated groundwater ranged from 0.01 to 0.1 mg l−1. However, when these soils were allowed to dry, the concentration of As released in the pore water decreased to undetectable levels. Remoistening of soils to field moisture over a 10-day period resulted in a significant (up to 0.06 mg l−1) release of As in the pore water of soils containing >10 mg As kg−1 soil, indicating the potential availability of As. In soils containing <5 mg As kg−1, As was not detected in the pore water. A comparison of Bangladeshi soils with strongly weathered long-term As-contaminated soils from Queensland, Australia showed a much greater release of As in water extracts from the Australian soils. However, this was attributed to the much higher loading of As in these Australian soils. The correlation of pore water As with other inorganic ions (P, S) showed a strongly significant (P < 0.001) relationship with P, although there was no significant relationship between As and other inorganic cations, such as Fe and Mn. Batch sorption studies showed an appreciable capacity for both AsV and AsIII sorption, with AsV being retained in much greater concentrations than AsIII.  相似文献   
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Bioremediation approaches for organic pollutants: a critical perspective   总被引:8,自引:0,他引:8  
Due to human activities to a greater extent and natural processes to some extent, a large number of organic chemical substances such as petroleum hydrocarbons, halogenated and nitroaromatic compounds, phthalate esters, solvents and pesticides pollute the soil and aquatic environments. Remediation of these polluted sites following the conventional engineering approaches based on physicochemical methods is both technically and economically challenging. Bioremediation that involves the capabilities of microorganisms in the removal of pollutants is the most promising, relatively efficient and cost-effective technology. However, the current bioremediation approaches suffer from a number of limitations which include the poor capabilities of microbial communities in the field, lesser bioavailability of contaminants on spatial and temporal scales, and absence of bench-mark values for efficacy testing of bioremediation for their widespread application in the field. The restoration of all natural functions of some polluted soils remains impractical and, hence, the application of the principle of function-directed remediation may be sufficient to minimize the risks of persistence and spreading of pollutants. This review selectively examines and provides a critical view on the knowledge gaps and limitations in field application strategies, approaches such as composting, electrobioremediation and microbe-assisted phytoremediation, and the use of probes and assays for monitoring and testing the efficacy of bioremediation of polluted sites.  相似文献   
18.
Toxicity studies considering both the bare and stabilized forms of zero valent iron nanoparticles (nZVI) could be timely, given that ecological risks identified are minimized through modification or with substitution of approaches in the synthesis, development and environmental application of the nanoparticles before succeeding to volume production. This review is focused on the fate, transport and toxicological implications of the bare nZVI and surface modified particles used for environmental applications.  相似文献   
19.
The influence of ionic strength, index cations and competing anions on arsenate (AsV) adsorption–desorption kinetics was studied in an Alfisol soil. A flow-through reactor system similar to that developed by Carski and Sparks (Soil Sci Soc Am J 49:1114–1116, 1985) was constructed for the experiments. Arsenate adsorption kinetics for all the treatments were initially fast with 58–91% of AsV adsorbed in the first 15 min. Beyond 15 min, AsV adsorption continued at a slower rate for the observation period of the experiments. Changes in the solution composition had differing effects on the cumulative amount of AsV adsorbed by the soil. Ionic strength and different index cations had little effect on the amount of AsV adsorbed, while the presence of phosphate decreased the amount of AsV adsorbed from 169 to 89 and 177 to 115 g AsV μg−1 in 0.03 M sodium nitrate and 0.01 M calcium nitrate, respectively. Considerably less AsV was desorbed than was adsorbed, with only between 2 to 17% of the adsorbed AsV desorbed. The presence of phosphate increased the amount of AsV desorbed by 17%, but other changes in the solution ionic strength or index cation had little effect on the amount of AsV desorbed.  相似文献   
20.
The acute toxicity of arsenic(III) and arsenic(V) alone and in combination to a cladoceran, Daphnia carinata, was studied in both cladoceran culture medium and natural water collected from a local suburban stream. As(III) was found to be more toxic than As(V) to Daphnia survival. The LC50 values for As(III), As(V), and As(III) + As(V) were 0.554, 1.499, and 0.692 mg l−1, respectively. Although various species of As, particularly As(III) and As(V) co-exist together in natural waters, the existing guidelines for water quality are based on individual As species. The results of this investigation suggest that As(III) and As(V) can interact either synergistically or additively resulting in an increase in the overall toxicity of the mixture compared to individual As species. Also, indigenous microorganisms in natural water may play a significant role in the transformation of As, thereby influencing the toxicity of As in receiving waters. This study clearly suggests that the joint action of As species should be considered in the development of water quality guidelines. To our knowledge this is the first study on the interactive effect of As(III) and As(V) to a cladoceran. Thus, this study suggests that these two species of As, when present together above 0.1 mg l−1 concentration, are toxic to fresh water invertebrates; therefore, pollution with these compounds may adversely affect natural ecosystems.  相似文献   
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