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1.
污染土壤毒性研究方法进展   总被引:1,自引:0,他引:1  
综述了国内外有关污染土壤毒性研究方法,包括传统的方法如植物法、动物法和微生物法等和生态毒理学方法,并从生物、非生物和环境等方面论述了影响土壤毒性的因素,提出了当前土壤污染毒性研究方法中存在的问题,认为随着环境科学技术的发展,污染土壤毒性研究方法在环境保护中必将发挥越来越重要的作用。  相似文献   

2.
邻苯二甲酸酯(PAEs)是一类环境激素类化合物,具有致畸、致癌和致突变的毒性。土壤中的PAEs可以通过食物链在人体内富集,威胁人类身体健康。当前土壤受PAEs污染现象日益普遍,选择合适的提取和检测方法评估土壤的PAEs污染程度显得至关重要。在前人研究成果的基础上,比较了索氏提取法、振荡提取法等传统方法与加速溶剂提取法等新型方法共7种土壤样品提取方法的优缺点,并综述了国内外检测土壤样品中PAEs含量的主要方法。展望了土壤中PAEs提取方法的发展趋势,为今后高效、快速检测土壤中的PAEs污染状况提供科学依据。  相似文献   

3.
污染场地环境的调查诊断是污染场地风险管理的重要环节和依据,迄今为止中国在污染场地土壤生态毒性诊断方面尚未形成系统的技术方法。借鉴了发达国家在土壤生态毒性诊断方面的相关经验,从保护土壤功能(保持功能、栖息地功能)的角度出发,结合污染场地现在或未来土地利用类型,建立了污染场地土壤生态毒性诊断方法的筛选程序,包括污染场地初步调查、生态毒性诊断方法初筛和生态毒性诊断方法复筛3个阶段。该筛选方法在某铅蓄电池污染场地进行了应用,为中国污染场地土壤生态毒性诊断的规范化提供了参考。  相似文献   

4.
在实施污染土壤修复的环境工程后,需要通过灵敏和有效的评定方法对污染土壤修复的效果进行评定.然而,单纯依靠化学方法进行污染土壤修复效果的评定,不能揭示土壤的整体质量特征,因此需要生态毒理方法作为相互补充的手段.本文概述了植物毒性评定法、陆生无脊椎动物评定法和土壤微生物评定法及其在污染土壤修复效果评定中的应用,并对污染土壤修复效果评定方法的发展前景进行展望.  相似文献   

5.
基于GCM_CB模型的土壤重金属污染评价   总被引:2,自引:0,他引:2  
灰色聚类法已经运用于土壤重金属污染评价中,然而此法在确定聚类权重时仅考虑重金属浓度,忽略了衡量重金属毒性强弱的重要指标生物毒性指数。为了更客观和准确地反映土壤重金属的污染程度,将生物毒性指数引入到聚类指标权重中,构建GCM_CB(grey clustering method_concentration and biotoxicity)土壤重金属污染评价模型。通过对华东某地区的10个区域土壤重金属污染进行分析评价,并与常用评价方法对比研究,表明:其多数样点的评价结果基本一致,但针对样品4和样品9中的元素Hg,因其强毒性,使得评价等级由I级定为II级,从而提高了评价方法的灵敏度,更加符合该区域的实际土壤污染情况。  相似文献   

6.
污染土壤修复效果评定方法的研究   总被引:7,自引:0,他引:7  
在实施污染土壤修复的环境工程后,需要通过灵敏和有效的评定方法对污染土壤修复的效果进行评定。然而,单纯依靠化学方法进行污染土壤修复效果的评定,不能揭示土壤的整体质量特征,因此需要生态毒理方法作为相互补充的手段。本文概述了植物毒性评定法、陆生无脊椎动物评定法和土壤微生物评定法及其在污染土壤修复效果评定中的应用,并对污染土壤修复效果评定方法的发展前景进行展望。  相似文献   

7.
汞是常温常压下唯一以液态存在的金属,由于其高挥发性和剧毒性,排放到环境中容易造成严重的污染。而且,长期暴露在汞含量超标的环境中对人体具有极大的伤害。主要综述了当前应用吸附法治理气体、水体和土壤中汞污染的研究进展,并指出生物吸附技术是今后治理重金属污染的重要发展方向。  相似文献   

8.
以盐城海岸带为研究区,分别采用地质累积指数法、内梅罗指数法和潜在生态危害指数法对土壤重金属污染进行风险评价,分析不同方法在评价同一研究区时结果的差异性。结果表明,研究区Cr、Ni、Zn、Cd质量浓度平均值超过盐城海岸带环境背景值。地质累积指数法显示研究区土壤重金属在中度污染到强污染;内梅罗指数法显示研究区土壤重金属为重度污染;潜在生态危害指数法显示研究区土壤重金属处于中度潜在生态危害程度。3种方法评价结果的严重程度为:内梅罗指数法地质累积指数法潜在生态危害指数法。3种评价方法均有一定缺陷与局限性,相对于单一方法的污染评价,采用多种方法评价土壤重金属污染可使评价结果更加客观。  相似文献   

9.
表面活性剂冲洗修复多氯联苯污染土壤多相流研究   总被引:3,自引:1,他引:2  
多氯联苯(PCBs)是一种具有持久性、抗生物降解性、脂肪溶性和明显的生物毒性等特性的持久性有机污染物,PCBs在土壤中难于准确定位、难被分解和强烈吸附,去除土壤中PCBs比较困难.表面活性剂冲洗法可以通过提高PCBs溶解度和降低水-PCBs界面张力来实现PCBs从土壤中去除;表面活性剂冲洗PCBs污染土壤涉及气相、水相、NAPLs相和固相等物质,是多相共存并相互发生作用的过程,发生相对渗透率、饱和度和毛细压力的变化;另外,为研究表面活性剂冲洗土壤中PCBs的去除机理,并降低PCBs对研究人员的危害,采用微观孔隙结构网络模型是一种较新颖的和效果显著的研究方法.开展表面活性剂冲洗PCBs污染土壤多相流研究,可以为PCBs污染场地修复提供理论基础和实验支持,并促进我国POPs履约工作的顺利进行.  相似文献   

10.
Pb与1,2,4-三氯苯单一及复合污染对蚯蚓毒性机制的研究胡艳祝飞王艳吴石金(浙江工业大学生物与环境工程学院,浙江杭州310014)以赤子爱胜蚓(Eisenia Foetida)作为受试生物,研究了土壤中Pb2+与1,2,4-三氯苯单一及复合污染对蚯蚓的毒性机制。通过滤纸接触法研究Pb2+与1,2,4-三氯苯的单一急性毒性效应,结果表明,两者对赤子爱胜蚓均有毒性。染毒48 h时,Pb2+的半数致死浓  相似文献   

11.
We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.  相似文献   

12.
Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for 3H, 90Sr, 137Cs, totU, 238Pu, 239,240Pu, and 241Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of 90Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g‐1 [126E‐02 Bq kg‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g‐1 [518E‐02 Bq kg‐1]). The differences in 90Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y‐1 (1.0 ± 1.0 μSv y‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y‐1 (1000 μSv y‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.  相似文献   

13.
14.
Approximately 25, 000-35, 000 dry cleaning facilities currently operate in the U.S. The release of perchloroethylene and other solvents from these establishments represents a major source of soil and groundwater contamination. The manner in which dry cleaning solvents escape from dry cleaning plants is, for all practical purposes, identical for chlorinated and petroleum hydrocarbon solvents and is related to one of the following events: the catastrophic failure of a component of the dry cleaning system, the improper installation, operation or maintenance of the dry cleaning equipment or a combination of all of these causes. Acceptable customs, codes and regulations can also dictate what is authorized for operation of a dry cleaning facility in a particular community, geographic area during a particular time frame. Environmental litigation dealing with the origin of a solvent release from dry cleaners tends to focus on the design and manufacture of dry cleaning industry machines such as washers, washer extractors, tumblers, solvent filters, water separators, stills and spotting boards. A thorough analysis of the daily operations of dry cleaners often reveals that poor maintenance, failure to follow the manufacturer's instructions and the actions of the operator are the most likely causes of soil and groundwater pollution. In order to forensically evaluate the most probable origins of a solvent release and to examine issues regarding liability, a thorough understanding of the history of dry cleaning and a detailed analysis of the operation and maintenance of the dry cleaning equipment are necessary. The discovery of solvent plumes in the vicinity of dry cleaning plants may suggest that the solvent source is the dry cleaning plant; however, the presence of these plumes does not necessarily indicate that the dry cleaning equipment was defectively designed or manufactured. A thorough review of the type of equipment used over the life of the dry cleaning plant and verifiable solvent mileage records frequently indicates that operators of the plant have disposed of solvent and contaminated solids into the municipal sewer or on ground surfaces.  相似文献   

15.
Abstract

This paper summarizes radionuclide concentrations (3H, 90Sr, 137Cs, 238Pu, 239,240Pu, 241Am, and totU) in muscle and bone tissue of mule deer (Odocoileus hemionus) and Rocky Mountain elk (Cervus elaphus) collected from Los Alamos National Laboratory (LANL), Los Alamos, New Mexico, lands from 1991 through 1998. Also, the committed effective dose equivalent (CEDE) and the risk of excess cancer fatalities (RECF) to people who ingest muscle and bone from deer and elk collected from LANL lands were estimated. Most radionuclide concentrations in muscle and bone from individual deer (n = 11) and elk (n = 22) collected from LANL lands were either at less than detectable quantities (where the analytical result was smaller than two counting uncertainties) and/or within upper (95%) level background (BG) concentrations. As a group, most radionuclides in muscle and bone of deer and elk from LANL lands were not significantly higher (p<0.10) than in similar tissues from deer (n = 3) and elk (n = 7) collected from BG locations. Also, elk that had been radio collared and tracked for two years and spent an average time of 50% on LANL lands were not significantly different in most radionuclides from road kill elk that have been collected as part of the environmental surveillance program. Overall, the upper (95%) level net CEDEs (the CEDE plus two sigma for each radioisotope minus background) at the most conservative ingestion rate (50 lbs of muscle and 13 lbs of bone) were as follows: deer muscle = 0.22 mrem y‐1 (2.2 μSv y‐1), deer bone = 3.8 mrem y‐1 (38 μSv y‐1), elk muscle = 0.12 mrem y‐1 (1.2 μSv y‐1), and elk bone = 1.7 mrem y‐1 (17 μSv y‐1). All CEDEs were far below the International Commission on Radiological Protection guideline of 100 mrem y‐1 (1000 μSv y‐1), and the highest muscle plus bone net CEDE corresponded to a RECF of 2E‐06, which is far below the Environmental Protection Agency upper level guideline of 1E‐04.  相似文献   

16.
This study aimed to evaluate the leaching of pesticides and the applicability of the Attenuation Factor (AF) Model to predict their leaching. The leaching of carbofuran, carbendazim, diuron, metolachlor, α and β endosulfan and chlorpyrifos was studied in an Oxisol using a field experiment lysimeter located in Dom Aquino – Mato Grosso. The samples of percolated water were collected by rain event and analyzed. Chemical and physical soil attributes were determined before pesticide application to the plots. The results showed that carbofuran was the pesticide that presented a higher leaching rate in the studied soil, so was the one representing the highest contamination potential. From the total carbofuran applied in the soil surface, around 6 % leached below 50 cm. The other pesticides showed lower mobility in the studied soil. The calculated values to AF were 7.06E-12 (carbendazim), 5.08E-03 (carbofuran), 3.12E-17 (diuron), 6.66E-345 (α-endosulfan), 1.47E-162 (β-endosulfan), 1.50E-06 (metolachlor), 3.51E-155 (chlorpyrifos). AF Model was useful to classify the pesticides' potential for contamination; however, that model underestimated pesticide leaching.  相似文献   

17.
Endosulfan in China 2—emissions and residues   总被引:4,自引:0,他引:4  
Background, aim, and scope  Endosulfan is one of the organochlorine pesticides (OCPs) and also a candidate to be included in a group of new persistent organic pollutants (UNEP 2007). The first national endosulfan usage inventories in China with 1/4° longitude by 1/6° latitude resolution has been reported in an accompanying paper. In the second part of the paper, we compiled the gridded historical emissions and soil residues of endosulfan in China from the usage inventories. Based on the residue/emission data, gridded concentrations of endosulfan in Chinese soil and air have been calculated. These inventories will provide valuable data for the further study of endosulfan. Methods  Emission and residue of endosulfan were calculated from endosulfan usage by using a simplified gridded pesticide emission and residue model—SGPERM, which is an integrated modeling system combining mathematical model, database management system, and geographic information system. By using the emission and residue inventories, annual air and soil concentrations of endosulfan in each cell were determined. Results and discussion  Historical gridded emission and residue inventories of α- and β-endosulfan in agricultural soil in China with 1/4° longitude by 1/6° latitude resolution have been created. Total emissions were around 10,800 t, with α-endosulfan at 7,400 t and β-endosulfan at 3,400 t from 1994 to 2004. The highest residues were 140 t for α-endosulfan and 390 t for β-endosulfan, and the lowest residues were 0.7 t for α-endosulfan and 170 t for β-endosulfan in 2004 in Chinese agricultural soil where endosulfan was applied. Based on the emission and residue inventories, concentrations of α- and β-endosulfan in Chinese air and agricultural surface soil were also calculated for each grid cell. We have estimated annual averaged air concentrations and the annual minimum and maximum soil concentrations across China. The real concentrations will be different from season to season. Although our model does not consider the transport of the insecticide in the atmosphere, which could be very important in some areas during some special time, the estimated concentrations of endosulfan in Chinese air and soil derived from the endosulfan emission and residue inventories are in general consistent with the published monitoring data. Conclusions  To our knowledge, this work is the first inventory of this kind for endosulfan published on a national scale. Concentrations of the chemical in Chinese air and agricultural surface soil were calculated for each grid cell. Results show that the estimated concentrations of endosulfan in Chinese air and soil agree reasonably well with the monitoring data in general. Recommendations and perspectives  The gridded endosulfan emission/residue inventories and also the air and soil concentration inventories created in this study will be updated upon availability of new information, including usage and monitoring data. The establishment of these inventories for the OCP is important for both scientific communities and policy makers.  相似文献   

18.
This study is aimed at investigating the impact of water quality on the uptake and distribution of three non-essential and toxic elements, namely, As, Cd and Pb in the watercress plant to assess for metal toxicity. The plant was hydroponically cultivated under greenhouse conditions, with the growth medium being spiked with varying concentrations of As, Cd and Pb. Plants that were harvested weekly for elemental analysis showed physiological and morphological symptoms of toxicity on exposure to high concentrations of Cd and Pb. Plants exposed to high concentrations of As did not survive and the threshold for As uptake in watercress was established at 5 ppm. Translocation factors were low in all cases as the toxic elements accumulated more in the roots of the plant than the edible leaves. The impact of Zn on the uptake of toxic elements was also evaluated and Zn was found to have an antagonistic effect on uptake of both Cd and Pb with no notable effect on uptake of As. The findings indicate that phytotoxicity or death of the watercress plant would prevent it from being a route of human exposure to high concentrations of As, Cd and Pb in the environment.  相似文献   

19.
Concentrations of mono- (MBT), di- (DBT), and tri-(TBT) butyltin compounds were measured in eggs, liver, and muscle of nine species of fish from four regions of the Baltic Sea - the Firth of Vistula, the Gulf of Gdańsk, Puck Bay, and the mouth of the Vistula River. The overall concentration ranges among all the fish sampled from the four sites were: < 7 to 79 ng/g for MBT, 6 to 1100 ng/g for DBT, 7 to 3600 ng/g for TBT, and 16 to 4800 ng/g for total BTs, on a wet wt basis. The highest concentration of total BTs was found in herring liver from the Firth of Vistula (4800 ng/g, wet wt) and in roach muscle from Puck Bay (3300 ng/g, wet wt), while the least concentration was found in burbot eggs and liver from the Vistula River (39 and 32 ng/g, wet wt, respectively). TBT was the major form of BTs present in most samples analyzed. Sediment samples collected from shipyards in the Gulf of Gdańsk contained butyltin concentrations ranging from 1.2 to 46 μg/g (dry wt) for MBT, 2.0 to 42 μg/g for DBT, and 2.6 to 40 μg/g for TBT. As with the fish, the majority of the BTs in sediment were present as TBT, which suggested recent exposure of the aquatic environment of the region to TBT.  相似文献   

20.
The effect of malathion [diethyl(dimethoxythiophosphorylthio)succinate] at sublethal concentration (0.006 ppm) on hematological parameters of the cricket frog (Fejervarya limnocharis) was studied for 24 hrs to 240 hrs of exposure and remarkable hematological alterations were observed. The study on hematological parameters revealed a highly significant decrease (P < 0.01) in the total erythrocytes count in malathion-exposed animals from 24 hours to 96 hrs of exposure as compared to control. Significant decreases (P < 0.01) of hemoglobin and packed cell volume were also observed from 48 hrs to 240 hrs. A significant increase (P < 0.01) in leucocytes count was noted throughout the exposure period. Elevated numbers of lymphocytes and eosinophils as found in the present study revealed lymphocytosis as well as eosinophilia, suggesting that this was a result of direct stimulation of the immunological defense due to the presence of a toxic substance or may be associated with tissue damage. The cytomorphological and cytopathological study of erythrocytes and leucocytes in malathion-exposed frogs at 0.006 ppm concentration revealed various cytotoxic effects at different exposure times. It was noted that the size and the shape of the erythrocytes were subjected to variation in different blood disorders.  相似文献   

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