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1.
南运河生态修复水体有机污染物的污染特征   总被引:1,自引:0,他引:1  
通过向水体投加高效微生物净水剂和生物复合酶生态修复南运河受污染水体.为研究南运河生态修复水体中持久性有机氯农药(Organochlorine pesticides,OCPs)、多环芳烃(Polycyclic aromatic hydrocarbons,PAHs)和有机磷农药(Organophosphorus pesticide,OPPs)污染特征,监测了南运河及生态修复试验河道水体中15种OCPs、17种PAHs和18种OPPs的含量.结果表明,南运河水体及试验河道表层水体中共检测出3种六六六类(Hexachlorocyclohexanes,HCHs)污染物,分别是α-六氯环己烷(α-HCH)、β-六氯环己烷(β-HCH)和林丹(γ-HCH),OCPs总量变化范围是1.11—1.78 ng·L~(-1);共检测出萘(Naphthalene,Nap)、苊(Acenaphthene,Ac P)、苊烯(Acenaphthylene,Ac Py)等11种PAHs,PAHs总量变化范围是52.76—60.28 ng·L~(-1);共检测出3种OPPs,分别是甲胺磷(Methamidophos,MTP)、敌敌畏(Dichlorvos,DDVP)、和甲基异柳磷(Isofenphos-methyl,IPM),OPPs总量变化范围是6.51—17.50 ng·L~(-1).微生物净水剂和生物复合酶的投加基本上不能降解水体中的OCPs和PAHs,而对水体中OPPs的降解有一定作用,降解率在19.6%—62.8%之间,平均降解率为35.2%.高效微生物净水剂和生物复合酶降解河道水体中持久性OCPs、PAHs和OPPs的机理有待进一步研究,该技术对河流、湖泊有机污染物生态修复实际应用具有一定的借鉴作用.  相似文献   

2.
近10年来,大批农药、化工企业迁出江苏南部地区,为了解该地区有机氯农药的残留状况以及环境行为,首次对南京、镇江、常州、无锡、苏州部分农业区和工业区浅层土壤中22种有机氯农药(OCPs)的分布特征进行研究,采用加速溶剂萃取法(ASE)和气相色谱法(GC-ECD),对30个不同深度样品进行检测。结果表明:表层土壤依旧是OCPs的主要残留层,主要为滴滴涕(DDTs)和六六六(HCHs)类污染,其中,ω(DDTs)为ND~313.0 ng·g-1(干重,下同),平均值75.04ng·g-1;ω(HCHs)为ND~9.25 ng·g-1,平均值2.82 ng·g-1。DDTs残留以降解代谢产物p,p′-DDD和p,p’-DDE为主,HCHs残留则以β-HCH为主。此外,六氯苯(HCB)、艾氏剂(Aldrin)、七氯(Heptachlor)、狄氏剂(Dieldrin)和硫酸硫丹(Endosulfan sulfate)也有不同程度检出。不同利用类型表层土壤中,有机氯残留状况有所差异,DDTs在工业区土壤中残留量最高,而HCHs在农业区土壤中残留量最高,OCPs残留平均值为工业区(127.2 ng·g-1)农业区(30.75 ng·g-1)。垂向土壤样品分析结果表明:大部分点位OCPs、DDTs及HCHs的残留量均随土壤深度增加而降低,但在下降过程中存在一定的波动性,由于场地土壤受到人为活动的影响,存在一定的干扰现象。本次调查未检出γ-HCH,仅有少量α-HCH检出,说明这些地区近期未出现林丹和HCHs输入。样品中(p,p′-DDD+p,p′-DDE)/DDTs的比值显示该地区近期新的外源DDTs输入较少。本次调查提供的数据可为该地区OCPs垂直分布研究提供参考。  相似文献   

3.
太原市污灌区地表土中有机氯农药分布特征   总被引:2,自引:0,他引:2  
为了研究太原市污灌区地表土中有机氯农药(OCPs)分布特征,本文在太原小店区共采集了31个地表土样,应用气相色谱-电子捕获检测器(GC-ECD)检测土壤中OCPs的含量.结果表明,研究区地表土中OCPs污染较轻,总OCPs浓度范围为2.01—47.20 ng.g-1(平均值为16.76 ng.g-1).其中总滴滴涕(∑DDT)浓度范围为0.27—37.93 ng.g-1(平均值为8.38 ng.g-1),总六六六(∑HCH)浓度范围为0.18—11.89 ng.g-1(平均值为3.37 ng.g-1),最高浓度均没有超过《土壤环境质量标准》(GB15618—1995)中的Ⅱ级标准(农业土地).不同灌溉区OCPs浓度平均值顺序为:污灌区>清灌区>背景点,表明污水回灌对OCPs浓度分布具有一定的影响,同时通过比较各采样点中OCPs各异构体的组成发现,该区域HCHs、DDTs和硫丹农药主要来自于历史残留,部分区域曾使用林丹和三氯杀螨醇农药.对比各有机氯农药浓度地理分布特征,表明OCPs浓度分布与污水灌溉存在一定的联系.  相似文献   

4.
利用同位素稀释质谱法测定了卧龙高海拔地区土壤中有机氯农药(OCPs)和低氯代多氯联苯(PCBs)的含量.海拔高度2800 m以上,土壤中HCHs和DDTs平均含量冬季(0.517和0.556 ng·g-1dw)高于夏季(0.293和0.323 ng·g-1dw).夏、冬两季的土壤中PCB28和PCB52含量浓度水平相近.以土壤干重表示的OCPs和低氯代PCBs含量随海拔升高而降低,而用有机碳归一化表示的含量随海拔升高而增加,证明了在卧龙高海拔地区存在着POPs的辛醇-空气分配系数与冷凝结效应相结合的富集现象.  相似文献   

5.
采用气相色谱质谱法测定了太湖沉积物柱状样品中有机氯农药(OCPs)含量,探讨了沉积柱中有机氯农药的垂直变化特征及可能的来源.研究结果表明:沉积柱中OCPs浓度为0.88—4.73 ng·g-1(干重),平均值为2.17 ng·g-1;DDTs、HCHs、六氯苯的残留量均较高,其中DDTs为0.10—1.32 ng·g-1,平均值为0.57 ng·g-1;HCHs的浓度为0.25—1.99 ng·g-1,平均值为0.65 ng·g-1;六氯苯为0.50—1.35 ng·g-1,平均值为0.92 ng·g-1.3个湖湾的沉积柱表层DDTs含量最高,有明显的表面富集现象,成分分析表明,太湖可能着存在着DDTs类物质的输入.  相似文献   

6.
多溴联苯醚(PBDEs)作为一种新型的持久性有机污染物,在海洋环境中广泛存在,研究PBDEs在不同介质中的赋存状态对于理解其环境行为及归趋具有重要的意义。通过采集不同区域沉积物及生物样品,考察了PBDEs在环渤海近岸海域表层沉积物及底栖生物中的含量及空间分布特征、污染模式及生物-沉积物富集因子。结果表明,环渤海沿岸表层沉积物中PBDEs总量(Σ10PBDEs)的浓度范围在0.446~26.8 ng·g-1(干重,dw)之间,中值为1.02 ng·g-1(dw),底栖生物中PBDEs(Σ9PBDEs)的浓度范围为0.053~9.90 ng·g-1(dw),中值为1.25 ng·g-1dw;沉积物中BDE-209为最主要的单体,平均丰度达到90.5%,生物体中主要以低溴代BDEs为主,其中单体BDE-47的含量最高,平均丰度范围为43.2%~49.7%;沉积物和生物中PBDEs的含量在空间上存在显著的差异,其中莱州湾和锦州附近区域的结果明显高于其他区域;5种不同的底栖生物对PBDEs均表现出一定的生物富集性,其中∑9PBDEs的BSAF值按从大到小的顺序为菲律宾蛤仔(0.43~4.06,mean=1.19)紫贻贝(0.34~2.86,1.03)四角蛤蜊(0.17~1.95,0.82)麻蛤(0.13~2.33,0.61)牡蛎(0.09~1.20,0.52)。辛醇水分配系数(log KOW)与不同物种BSAF值的相关性分析结果表明,除BDE-17单体外,其他单体的BSAF值表现出随log KOW的升高而下降的趋势。  相似文献   

7.
在黄河三角洲不同区域采集了26个土壤样品,利用GC-MS内标法测定土壤中22种有机氯农药(OCPs)含量,并对其残留特征、污染来源和生态风险进行了分析和评价.研究结果表明,土壤中共检测到19种OCPs,总的OCPs浓度范围为0.01—10.49 ng·g~(-1),平均浓度为1.678 ng·g~(-1).OCPs平均浓度顺序如下:DDTsHCHs氯丹类硫丹类,DDTs类农药的检出率最高,DDTs和HCHs是土壤中OCPs主要的组成成分,研究区土壤中DDTs和HCHs的残留水平低于国内其他地区土壤中含量,也低于规定的土壤阈值和土壤环境质量标准,本研究区土壤未受OCPs的污染.β-HCH和p,p'-DDE分别是HCHs和DDTs的主要组成成分.研究区土壤中OCPs主要来源于历史残留,无新的污染源输入.土壤中TOC和p H值对OCPs的残留存在影响,并且呈现弱的负相关性,不同类型土壤OCPs残留量存在差异,OCPs在树林土壤中的残留含量高于海岸带和原耕地土壤中.风险评价表明研究区土壤中HCHs农药残留量不会对生物产生风险;DDTs类农药对研究区生物存在可能性较小的生态风险,危害性总体较低.  相似文献   

8.
环境中有机磷农药污染状况、来源及风险评价   总被引:2,自引:0,他引:2  
环境中农药的污染残留问题备受社会关注,尤其是食品安全这一方面.作为世界上有机磷农药(OPPs)生产和使用的大国,国内环境中OPPs的残留赋存问题尤其受到重视.残留在环境中水体、土壤、生物体的OPPs可能经口、皮肤接触、呼吸等暴露途径进入人体对人体健康造成风险.了解OPPs在国内主要江河湖泊、土壤、生物体中的残留赋存情况并进行风险评价至关重要.本文对比总结了中国环境中水体、土壤、生物体中主要OPPs的含量范围、检出率及其分布特征,并利用美国RBCA健康风险评价模型对其进行健康风险评价和RQ商值法进行水生生态风险评价.结果显示,中国地表水体含量最高的5种OPPs分别是敌敌畏、乐果、对硫磷、马拉硫磷、甲基对硫磷,浓度变化范围ND—30180 ng·L~(-1),北方水体的OPPs污染状况水平要高于南方水体.OPPs风险评价结果显示,地表水、土壤、蔬菜中OPPs的非致癌风险系数(HQ)分别为7.25×10~(-5)—6.93×10~(-1)、9.56×10~(-7)—5.30×10~(-2)、1.08×10~(-2)—7.01×10~(-1),都还未超过1的安全标准,对人体健康不会产生明显的不良影响.地表水中敌敌畏的致癌风险系数(R)范围为2.86×10~(-8)—6.25×10~(-6)在10~(-5)—10~(-6)安全范围内.对比地表水、土壤、蔬菜的HQ值,蔬菜中残留的单体OPPs对人体的健康风险大于地表水和土壤,水生生态风险评价结果中OPPs对糠虾和水蚤RQ值1,处于高风险.  相似文献   

9.
本研究基于GC-MS分析了巢湖湖区及入湖河流共40个采样点的表层水及表层沉积物样品中有机氯杀虫剂(OCPs)的含量.研究结果表明,在一年内不同季节中,巢湖湖区及入湖河流表层水体∑OCPs浓度均较低,春季6.09—11.53 ng·L~(-1),夏季6.32—11.10 ng·L~(-1),秋季6.76—16.23 ng·L~(-1),冬季5.97—16.29 ng·L~(-1);相应季节OCPs平均浓度分别为8.33±1.19 ng·L~(-1),8.43±1.21 ng·L~(-1),9.25±1.96 ng·L~(-1)和8.33±2.14 ng·L~(-1).表层水体中OCPs主要为工业生产六六六(HCHs)以及杀虫剂林丹.湖区及入湖河流表层沉积物中OCPs浓度(ng·g~(-1)级别)远高于表层水体(ng·L~(-1)级别)的浓度,∑OCPs浓度范围为2.55—19.03 ng·g~(-1),平均浓度为5.80±4.07 ng·g~(-1),且巢湖西部地区OCPs污染大于东部区域,其中较高浓度的狄氏剂和硫丹成分说明巢湖区域受到这两类物质的污染.异构体分析表明,表层沉积物中OCPs的来源也与周边农田土壤和地表径流所带来的污染以及不同程度工业品HCHs粉剂和林丹的陆源性输入有关;在绝大多数采样点的表层沉积物中滴滴涕类农药(DDTs)的检出为历史的残留污染.生态风险评价表明,巢湖湖区及入湖河流表层水体中OCPs对该区域的生态风险几乎没有影响且表层沉积物中OCPs亦处于较低的风险状态.  相似文献   

10.
本研究以经济底栖生物菲律宾蛤仔和河蚬为受试生物,分别对不同浓度梯度的海洋和淡水底泥中9种代表性有机氯农药(OCPs)进行累积实验;同时采用Tenax连续萃取法研究2类底泥中OCPs的脱附动力学,提供简单、快速评价养殖底泥中OCPs生物有效性的方法,并将Tenax萃取结果与2种底栖生物的累积结果进行比较。结果表明,菲律宾蛤仔和河蚬对OCPs的生物-底泥富集因子(BSAF)分别为0.31~1.89和0.12~2.12,且底泥中有机碳标化的OCPs浓度与生物体内脂肪标化的OCPs浓度之间的相关性较差。Tenax脱附动力学的结果表明,2类底泥中OCPs的快速脱附比例(F_(rap))均在50%左右,其快速、慢速和极慢速脱附速率常数数量级分别为10~(~(-1))、10~(-2)和10~(-4)。Tenax快速脱附组分与2种底栖生物累积结果之间具有良好的相关性(r~2=0.75,P0.0001),表明Tenax萃取技术可以预测OCPs在底栖生物体内的累积量,并且该方法克服了大型底栖生物累积实验结果重复性较差等缺点。另外通过与基于热力学平衡的方法对比发现,Tenax萃取技术更适用于滤食性或可消化底泥的底栖生物对底泥污染物的富集;同时Tenax 6 h和24 h单点萃取技术可以作为简单快速评价底泥疏水性有机污染物(HOCs)生物有效性的替代方法,进一步为养殖领域的底泥污染状况以及相关水产品的质量安全和食用风险提供生物有效性评价依据。  相似文献   

11.
Spatial distribution, sources and potential health risks of organochlorine pesticides (OCPs), including hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT), in surface soils (n = 544) collected from a typical alluvial plain of the Yangtze River Delta region, China, were elucidated. Concentrations of ΣHCH and ΣDDT in soils ranged from less than the limit of detection (<LOD) to 99.0 ng g?1, dry weight (dw) (mean 3.23 ng g?1 dw) and <LOD to 600 ng g?1 dw (mean 88.8 ng g?1 dw), respectively. Historical applications of HCH and DDT were the major sources of the residue in soils. HCH was mainly distributed in Anthrosols in the southern part of the watershed, while DDT was mainly distributed in Cambosols in the northern part. The 95 % cumulative probability incremental lifetime cancer risks (ILCRs) of different age groups such as children, youths, and adults all exceeded the acceptable risk level of 10?6 recommended by USEPA for carcinogenic chemicals. The spatial distributions of ∑ILCRs were consistent with concentrations of OCPs in soils, while they were slight different for the different age groups. Adult females had the greatest risk of OCPs in soils, followed by children, while youths had the least risk. The ingestion of OCPs in soils was the more important route of exposure compared with dermal and inhalation exposures. The concentration of OCPs in soils, the particulate emission factor, the fraction of dermal exposure ratio, and the soil ingestion rate were the major contributing variables to total ILCRs according to sensitivity analyses.  相似文献   

12.
Organochlorines (including organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs)) were analysed in 10 surface sediment samples collected from the Bahiret el Bibane lagoon, which is one of the most productive lagoons and one of the most important active commercial fish traps in the southern Tunisia. The aim was to obtain information concerning the recent deposition of these compounds in this area, together with the levels, the distribution and any potential biological risk. Total concentrations of OCPs and PCBs in the sediments ranged from below the limit of detection (?1 and from 29.5 to 88.2?ng?g?1?dw, respectively. The spatial distribution of PCBs suggested that the sources of these contaminants are probably located outside the lagoon and are transported by water currents and atmospheric deposition. Compared with some other regions of the world, the Bahiret el Bibane lagoon exhibited low to moderate levels of PCBs and OCPs. According to established sediment quality guidelines, PCBs and Lindane at most of the study sites would be more concerned for the ecotoxicological risk in the Bahiret el Bibane lagoon. The results of this study could provide a useful aid for the sustainable marine management of the region.  相似文献   

13.
A systematic survey of organochlorine pesticides (OCPs) including hexachlorocyclohexane isomers (α-HCH, β-HCH, γ-HCH, δ-HCH and ΣHCH) and dichlorodiphenyltrichloroethane metabolites (p,p′-DDT, p,p′-DDE, o,p′-DDT, p,p′-DDD and ∑DDT) in soils along the north coastal areas of the Bohai Sea, China, has been lacking. In this study, 31 representative surface soil samples were collected along the north coastal and riverine areas of the Bohai Sea to characterise the potential for adverse effects of ∑HCH, ∑DDT and their individual isomers and transformation products. Concentrations of ΣHCH and ΣDDT in soils ranged from less than the limit of detection (1 ng · g?1 dw (mean: 3.5 ng · g?1 dw) and2 ng · g?1 dw (mean: 1.7 × 101 ng · g?1 dw), respectively. Compared with studies of OCPs in soils from other locations, concentrations of HCHs and DDTs observed in this study were moderate. Concentrations of OCPs observed in soils were generally less than proposed reference values. HCH residues were a mixture of historical technical HCH and current lindane sources. The pattern of DDTs was consistent with historical releases of technical DDTs. Selected soil physicochemical properties did not explain the sorption and/or partitioning of HCHs or DDTs.  相似文献   

14.
Contamination profiles of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) were determined in six fish species from three selected regions along coastal waters off Savannah, GA, USA. Concentrations of PCBs were predominant (12–493 ng g?1 lw) followed by PBDEs (10–337 ng g?1 lw), OCPs such as DDTs (2.7–153 ng g?1 lw), chlordanes (3.8–34 ng g?1 lw), cyclodienes (<0.1–35 ng g?1 lw), mirex (<0.1–8.6 ng g?1 lw), γ-hexachlorocyclohexane (<0.1–1.4 ng g?1 lw), and hexachlorobenzene (<0.1–0.68 ng g?1 lw). The results indicated no region-specific difference in the contaminants however inter-species as well as intra-species differences were evident. Comparison of DDTs, PCBs, and PBDEs profiles in fish with those from other countries revealed that fish from coastal waters off Savannah contained relatively less concentrations of PCBs and chlorinated pesticides, while PBDE concentrations were comparable or even higher than fish samples from other regions. Polychlorinated biphenyl congeners and chlorinated pesticide tempoal trend data exhibited no increase of contamination levels. The levels of PCBs and chlorinated pesticides in fish from Savannah coastal waters were below the Food and Drug Administrations (FDA) established limits for human consumption.  相似文献   

15.
Although use of pesticides is critical in agricultural production, their residues present a potential risk to non-target organisms and lower the quality of surface water. In Kenya for instance, widespread use of pesticides in the catchment of Lake Naivasha, has raised concern over the years due to possible pollution of the lake through discharge of runoff from agricultural fields. In this study, sediment, water, and fish samples were analyzed for selected pesticide residue contamination. Chlorpyrifos-ethyl (CPF) was detected in the range of 2.6–24.9 ng/ml and 6.8–35.8 ng/g dry weight (dw) in water and sediment, respectively. Meanwhile, diazinon was detected in the range of below detection limit (bdl) to 33.3 ng/ml and bdl to 9.3 ng/g dw in water and sediment, respectively. CPF was detected in fish tissues (Niloticus leucosticus) in the range of bdl to 8.9 ng/g dw with diazinon and carbofuran not detected in any fish sample. A significant difference was observed between different seasons with wet season recording higher levels. Concentrations detected varied seasonally and on average exceeded the maximum criterion set by European Union. Therefore, data generated in this study are useful in environmental risk assessment and as a baseline in formulation of mitigation measures to protect the lake from pesticides residues pollution.  相似文献   

16.
Organochlorine pesticides (OCPs) are pesticides with global scale ubiquity, persistence and bioaccumulation, which leave long-term residuals in the water body. OCPs’ high toxicity poses significant threats to human health and aquatic biodiversity, making assessment of OCPs’ impact on aquatic ecology and human health urgently necessary. In this research, the presence of 16 OCPs in surface water and groundwater along Shaying River, China, as well as OCPs concentration correlations, was investigated at 24 selected sampling sites. At the same time, the ecological risk and human carcinogenic risk were also analyzed by risk quotient method and USEPA’s Risk Assessment Guidance, respectively. Results showed that the total concentration of OCPs ranged from 21.0 to 61.4 ng L?1 in groundwater, and 12.3–77.5 ng L?1 in surface water. Hexachlorocyclohexane (HCHs) and heptachlor were the prominent contaminants in groundwater, which indicated their use in the recent past and confirmed their persistence. The α-HCH/γ-HCH ratios in groundwater confirmed that γ-HCH (lindane) was used as main substitute of technical HCH in the study area. The correlation analysis illustrated that δ-HCH and γ-HCH played a dominant role in HCHs residue. Heptachlor and α-HCH, as well as endosulfan and heptachlor epoxide, had a strongly significant positive correlation, suggesting an associated usage of the two pair OCPs. An extremely high ecological risk for aquatic organism was observed for γ-HCH, heptachlor and dieldrin, while the carcinogenic risks posed by the selected OCPs in surface water and groundwater were all acceptable.  相似文献   

17.
Soil is an important source to other environmental media and organisms for organochlorine pesticides (OCPs) bioaccumulation. Twenty-four representative surface soil samples were collected from the lower reaches of the Jiulong River, China, in 2009. The concentrations of hexachlorocyclohexane isomers (HCHs) ranged from 0.38 to 39.52 ng·g?1, with a mean value of 9.51 ng·g?1. The concentrations of dichlorodiphenyltrichloroethanes (DDTs) and their metabolites were within the ranges of 0.94–700.99 ng·g?1, with a mean value of 71.17 ng·g?1. The concentrations of HCHs and DDTs in the soil were lower than the first grade level (50 ng·g?1) of the Chinese Environmental Quality Standard (GB15618-1995). Hierarchical Cluster Analysis (HCA) and Pearson’s bivariate Correlations Analysis (PCA) were used to analyse the distribution and contamination levels of OCPs in this region. The results showed that DDTs were the major contaminants and there were no significant correlations between various OCPs concentrations and the total organic carbon (TOC) contents. A significant positive correlation was observed between HCHs and DDTs (p<0.01), which indicates that HCHs and DDTs may have similar sources and fate in the study area.  相似文献   

18.
从广东省西江流域三个饮用水源地采集三个样品,分别分析其中两类持久性有机污染物—有机氯农药和多环芳烃的含量以及来源,从这两类污染物对水环境污染的角度初步判断饮用水源的安全性。首先采用液液萃取的方法对样品进行前处理,然后分别用GC.ECD和GC—MS测定有机氯农药和多环芳烃的含量。实验发现有机氯农药质量浓度在水相中为1.99ng·L^-1~ 4.76ng·L^-1,在颗粒相中为0.36ng·L^-1~0.68ng·L^-1;多环芳烃质量浓度在水相中为73.40ng·L^-1~865.89ng·L^-1,在颗粒相中为16.76ng·L^-1~19.31ng·L^-1。结果表明,六六六和滴滴涕质量浓度低于国标《生活饮用水水源水质标准》(CJ3020.93)的规定,同时苯并[a]芘也低于世界卫生组织《饮用水水质标准》的规定,而其它物质标准中均无规定。由此说明,就有机氯农药和多环芳烃这两类污染物在水中的含量来说,广东西江领域饮用水源是相对安全的。但是由于这两类污染物都具有很强的生物富集性,因此它们在水环境中的存在和作用也是不容忽视的。  相似文献   

19.
In this study, the current situation of five types of toxic organics and endocrine disrupters in the sediments of rivers around Beijing, i.e., polycyclic aromatic hydrocarbons (PAHs), phthalic acid esters (PAEs), organic chlorinated pesticides (OCPs), estrogens (Es), and bisphenol A (BPA), which included 56 contaminants, was analyzed and compared with that registered by the historical literatures. The ecological risks were also assessed. The total concentration of PAHs, PAEs, OCPs, Es, and BPA ranged from 232.5 ng·g–1 to 5429.7 ng·g–1, 2047.2 ng·g–1 to 18051.5 ng·g–1, 4.5 ng·g–1 to 11.7 ng·g–1, 18.1 ng·g–1 to 105.2 ng·g–1, and 36.3 ng·g–1 to 69.6 ng·g–1, respectively. Among these five types of organic compounds, the concentration levels of PAHs and OCPs have decreased significantly in the last ten years, while those of PAEs and Es had an upward trend compared with the previous studies. BPA still remained at a moderately high level, as it was ten years ago. The risks of the PAEs in all of the sample sites, and fluoranthene, benzo[a]anthrene, and benzo[a]pyrene in the Wenyu River sediment, were relatively high. These results supplemented the database of toxic organics’ concentration levels in the sediments of Beijing rivers.
  相似文献   

20.
分析了水生(鲶鱼)和陆生(家鸽)生物体中卤系阻燃剂(HFRs)的组成和浓度。鲶鱼中短链氯化石蜡(SCCPs)浓度均值为30 800 ng·g~(-1)lw(脂肪归一化浓度),是最主要的HFRs,然后依次是多溴联苯醚(PBDEs)(2 300 ng·g~(-1)lw)、四溴双酚A(TBBPA)(37 ng·g~(-1)lw)、六溴环十二烷(HBCD)(21 ng·g~(-1)lw)、德克隆(DP)(14 ng·g~(-1)lw)、十溴二苯乙烷(DBDPE)(7.1 ng·g~(-1)lw)和六溴苯(HBB)(6.2 ng·g~(-1)lw);而家鸽中PBDEs含量最高(17 000 ng·g~(-1)lw),其次是SCCPs(7 600 ng·g~(-1)lw)DP(1 600 ng·g~(-1)lw)DBDPE(14 ng·g~(-1)lw)HBB、TBBPA和HBCDs(未检出)。鲶鱼和家鸽HFRs组成比较发现,鲶鱼中具有较高百分含量的低溴代PBDE单体和较低的fanti值,而家鸽中具有较高百分含量的高溴代PBDE单体和较高的fanti值。实验结果初步表明,水生生物较多地富集水溶性较大的化合物,陆生生物则较多地富集疏水性较强的化合物。研究认为以上水生和陆生生物体中污染物的差异性富集现象可能与化合物因不同物理化学性质导致的不同环境迁移行为有关。  相似文献   

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