超声波萃取-气相色谱/质谱法测定土壤中15种Pops类有机氯农药

用探头式超声波萃取仪、己烷/丙酮混合溶剂提取土壤中的15种Pops类有机氯农药(包括六氯苯、七氯、六六六、氯丹、艾氏剂、狄氏剂、异狄氏剂、灭蚁灵、滴滴涕),萃取溶液经氟罗里硅土柱净化、氮吹浓缩,用气相色谱/质谱仪(GC-MS)进行测定。方法检出限0.4～1.4μg/kg,空白样品有机氯农药加标回收率为52.8%～118%、有机氯标记替代物回收率为71.0%～122%,RSD为6.8%～16.5%。     

基于污染指数与ArcGIS的聊城市耕地OCPs污染研究

按8 km×8 km网格将聊城市耕地划分为136个采样点,调查六六六(BHCs)、滴滴涕(DDTs)、艾氏剂、狄氏剂、异狄氏剂、六氯苯和七氯等7种有机氯农药(OCPs)的残留状况。采用单因子污染指数和综合污染指数法进行污染评价,以此判断OCPs的污染程度。对7种OCPs在各样点中的含量进行差异分析,并应用ArcGIS8.3,以污染评价结果为数据支持,进行OCPs污染空间分布研究。结果表明,聊城市OCPs污染程度依次为DDTs>狄氏剂>七氯>艾氏剂>BHCs>异狄氏剂>六氯苯,总体变异程度依次为DDTs>狄氏剂>异狄氏剂>BHCs>七氯>六氯苯>艾氏剂。各OCPs空间分布没有固定的变化趋势;各采样点综合污染水平存在地域差异,以临清市污染最为严重,其他各县市污染较轻。     

G C/MS法测定环境空气中痕量POPs类有机氯农药及降解产物

采用快速溶剂萃取-氟罗里硅土柱净化-气相色谱/质谱联用法测定环境空气中POPs类有机氯农药及其降解产物.艾氏剂、狄氏剂、异狄氏剂、六六六、滴滴涕,七氯、氯丹、灭蚁灵及其降解产物的检出限为2.0 ng～4.6 ng,空白加标回收率为62.1%～118%,RSD为6.8%～15.2%.     

贵州农作物土壤中OCPs残留现状与差异性分析

通过在贵州主要农作物种植区域采集5 cm、10 cm、15 cm深度的土壤样品，检测其中22种OCPs的残留量。结果表明：在所有水稻土壤样品中除了环氧七氯-A、反式九氯和狄氏剂未检出外，其余19种OCPs均有不同程度检出；OCPs在上述3种深度土壤中总残留量分别为0.526 ng/g、0.497 ng/g、1.605 ng/g。DDTs在3种深度水稻土壤中的总残留量(0.359 ng/g)低于HCHs总残留量(1.135 ng/g)。水稻土壤中γ-HCH、δ-HCH残留量显著高于玉米土壤。水稻土壤中HCHs和硫丹残留主要源自历史上工业制剂的使用，DDTs在水稻土壤中的降解方式主要为厌氧。农作物种植区域土壤中OCPs残留量均符合国家农用地土壤污染风险管控标准。     

兰州西固区土壤中有机氯农药污染特征及风险评价

采集兰州西固区土壤样品,采用GC/μECD方法检测样品中有机氯农药(OCPs)污染残留,并分析调查区土壤中OCPs污染特征、来源及潜在生态风险。结果表明,8种OCPs异构体在兰州西固区土壤中的检出率均为100%,总质量比范围在18.34μg/kg~125.34μg/kg之间,平均值为54.84μg/kg;土壤中BCHs和DDTs残留质量比分别为0.742μg/kg~29.3μg/kg和10.9μg/kg~98.6μg/kg。OCPs残留以p,p'-DDT和β-BCH为主。不同采样点土壤样品中OCPs的残留量从高到低依次为路边样绿化带样树根土样菜地样。对DDTs与BCHs异构体残留组分分析发现,调查区土壤中残留的BCHs主要源于历史应用,而DDTs源于近期污染。     

POPs监测技术在环境样品中应用

利用超声提取、固相萃取(SPE)净化和GC-MS技术对某市四个区的的果蔬基地7个土壤样品进行了土壤中持久性有机氯污染物分析.结果显示,土壤样品中主要有机污染物为γ-HCH、异狄氏剂和α-HCH,其中γ-HCH的检出率为100%,不同样品中γ-HCH和异狄氏剂差异明显,异狄氏剂和α-HCH检出率分别为86%和71.4%.     

珠江三角洲城市群及高海拔地区表层土中有机氯农药的空间分布特征

利用GC-ECD方法测定了珠江三角洲城市群及高海拔地区表层土壤中的有机氯农药。有机氯农药变幅为2.4~78.7 ng/g,平均15.9 ng/g。最高值出现在江门。总HCHs变幅为ND~19.2 ng/g,平均2.91 ng/g, 最高值出现在佛山。总DDTs变幅为ND~74.6 ng/g,平均值为9.91 ng/g。最高值出现在东莞。六氯苯在佛山较高。灭蚁灵在深圳的污染较其它地区严重。总体来说,HCHs污染程度较低,但部分地区有林丹的使用;有些采样点DDTs的污染程度超过了国家土壤环境质量标准的一级自然背景值,且有些区域可能有非三氯杀螨醇的DDTs外源输入。     

气相色谱法测定赤水河中段水体中14种有机氯农药的残留

建立了用正己烷萃取,气相色谱—电子捕获（GC—ECD）测定水体中有机氯农药痕量残留的方法。结果表明：六氯苯、α-HCH、β-HCH、γ-HCH、δ-HCH、p,p′-DDD、p,p′-DDE、p,p′-DDT、艾氏剂、狄氏剂、异狄氏剂、七氯、环氧七氯、o,p′-DDT 14种农药在14 min内有较好的分离;2个不同浓...     

有机氯农药在湖北省菜地土壤中的污染研究

采集了湖北省武汉、宜昌、襄阳地区的45个菜地土壤样品,测定其中11种有机氯农药的残留量,并对其残留特征和污染来源进行了研究分析。结果表明,所有土壤样品中均检出有机氯农药,但大多数点位的污染物含量均低于相关标准限值,通过数据统计和因子分析法得出p,p’-DDT、p,p’-DDE为主要污染物。计算特征比值后发现,该地区滴滴涕污染可能源于传统工业滴滴涕和三氯杀螨醇的混合源,既有早期污染也有新污染的输入,六六六污染主要源于林丹,氯丹残留主要源于早期污染。     

两种有机氯农药在污水灌溉区蔬菜中的残留及生物富集

于污水灌溉区种植的6种蔬菜中均检测出有机氯农药(OCPs),六六六(HCHs)含量高于滴滴涕(DDTs).6种蔬菜对OCPs在不同程度上有富集作用,蔬菜种类不同,对HCHs、DDTs各异构体的富集能力不同.各类蔬菜均为微污染.     

Tiered aquatic ecological risk assessment of organochlorine pesticides and their mixture in Jiangsu reach of Huaihe River, China

A tiered approach consisting of several probabilistic options was used to refine aquatic ecological risk assessment (ERA) of individuals and mixture of various Organochlorine Pesticides (OCPs) detected in Jiangsu reach of Huaihe River, China. The tiered approach ranged from determined Hazard Quotient (HQ) to Joint Probability Curve and Monte Carlo simulation based HQ-distribution. The results from all levels of ERA methods in the tiered framework are consistent with each other. The results show that Endrin, o,p'-Dichloro-Diphenyl-Trichloroethane (DDT), alpha-Endosulfan and beta-Endosulfan posed clear ecological risk; p,p'-DDT, p,p'-DDD, Aldrin, Heptachlorepoxide and Methoxychlor posed potential risk; while Hexachlorocyclohexanes, Heptachlor, Dieldrin and Hexachlorobenzene posed negligible risk. Further, based on the concept of total equivalent concentration, combined ecological risk caused by the mixture of all detected OCPs was calculated, and it proved to be significantly higher than the risk caused by any individual OCP. Despite inevitable uncertainties in current ERA, a comprehensive tiered approach can help to get a more credible result of risks of individuals and mixture of hazardous pollutants and screen the major risk pollutants contributing to the combined ecological risk.     

Monitoring and Assessment of Persistent Organochlorine Residues in Sediments from the Daliaohe River Watershed, Northeast of China

Surface sediment samples from 12 sites of the three selected rivers in Daliaohe River watershed (Hunhe River, Taizihe River and Daliaohe River) were analyzed with the objective of establishing sources and hazard of the organochlorinae pesticides (OCPs) and polychlorinated biphenyl (PCBs) in surface sediments. The total concentrations of OCPs varied from 3.06 to 23.24 ng g⁻¹. ∑HCH (α-HCH, β-HCH, δ-HCH, γ-HCH), ∑DDT (p, p′-DDE, p, p′-DDD, o, p′-DDT, p, p′-DDT) and ∑Cyclodiene (Heptachlor, Aldrin, Heptachlor epoxide, Dieldrin, Endrin) ranged from 1.86 to 21.48, 0.5 to 2.81 and 0.56 to 1.53 ng g⁻¹, respectively. Results of OCPs also illustrate that the most dominant pollutants among the OCPs was ∑HCH, and γ-HCH was the most dominant isomer in HCH, which was evidence of recent input of lindane. It possibly came from the runoff of polluted soils and long-scale transportation. Total PCB concentrations ranged between 1.88 and 16.88 ng g⁻¹. The peak concentrations of PCBs were found in sediments from station T5 and D3, which are in the vicinity of industrial areas and ferry, respectively. These data show a moderate level of OCPs and PCBs contaminations compared to that in other countries.     

The Contamination Levels of Organochlorine Pesticides in Water and Sediment Samples in Uluabat Lake, Turkey

The Uluabat Lake is a reservoir of 125 km² surface area, in the boundaries of Bursa province, Turkey. The results showed that Uluabat Lake was still contaminated by organochlorine pesticides and their residues despite the existence of bans over a long time. Considerable amounts of organochlorine pesticides (HCB, p.p^′-DDT, p.p^′- DDE, α -, β- and γ-BHC, Aldrin, Heptachlor epoxide, Endrin, Endosulfan I and II) were detected in water and sediment samples during one-year study in this lake. Samples of water and sediment were collected in different regions, (6 sampling point) of the lake between February 2002 and November 2002.The mean levels of organochlorine pesticides in water and sediments were determined. According to results, it was found that various environs in Uluabat Lake were contaminated by 11 different organochlorine pesticides. Residue analyses showed that higher organochlorine pesticides and their residues were generally more accumulated in the sediment samples.     

Organochlorine contamination in shorebirds from Washington state and the significance for their falcon predators

Arctic-breeding shorebirds collected in western Washington state during winter and spring, and a comparative sample collected in coastal California during the winter were analyzed for organochlorine contaminants to determine the potential impact of these residues on populations of peregrine falcons (Falco peregrinus) and merlins (F. columbarius) which prey upon shorebirds in western Washington. Dunlins (Calidris alpina), an important winter prey for falcons in western Washington, were collected between 1975 and 1981. During winter 1980–81, dunlins carried low organochlorine residues; DDE levels ranged from 0.01 to 1.2 ppm, and PCB levels ranged from 0.02 to 0.82 ppm (wet weight). Levels of other organochlorine contaminants (HCB, Chlordane compounds, Dieldrin, and Heptachlor Epoxide), analyzed in a subsample of dunlins, were consistently lower than DDE and PCB levels, and ranged from 0.001 to 0.22 ppm (wet weight). Dunlins in western Washington did not significantly increase their DDE or PCB burdens over the 1980–81 winter. A decline in DDE residues between 1978 and 1981 was noted, and declines in PCB residues from both 1975 and 1978 to 1980–81 were noted. Residues in other wintering shorebirds from western Washington were similar. Wintering sanderlings (Calidris alba) from California, revealed much higher DDE contamination than in Washington (up to 32 ppm, wet weight). Spring migrant shorebirds in western Washington contained both low and very high DDE residues (up to 417 ppm, wet weight). There is evidence suggesting these high DDE concentrations are accumulated along the Pacific coast of North America.     

Occurrence and characterization of selected organochlorine contaminants in outdoor dust collected from Xinxiang,a fast developing city in North China

As facile “environmental media”, the outdoor dust may reflect the changes of contaminants in environment more promptly. In the present study, selected organochlorine contaminants (OCs) include hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), hexachlorobenzene (HCB), and pentachlorobenzene (PeCB) were detected in 20 outdoor dust samples collected from Xinxiang City. The concentrations of ΣHCHs, ΣDDTs, HCB, and PeCB in dust were in the range of 0.18–5.05 ng/g dry weight, 0.44–13.50 ng/g dry weight, 0.13–51.61 ng/g dry weight and ND-0.74 ng/g dry weight, respectively. Long-range transport, historical use, and recent impact of impure pesticides might be the main sources of OCs in the outdoor dust. The results of this study indicated that impure pesticide application maybe an important source of DDTs and HCB in the environment.     

Regional differences and sources of organochlorine pesticides in soils surrounding chemical industrial parks

Concentrations of organochlorine pesticides (OCPs; dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB)) were investigated in 105 soil samples collected in vicinity of the chemical industrial parks in Tianjin, China. OCP concentrations significantly varied in the study area, high HCH and DDT levels were found close to the chemical industrial parks. The intensity of agricultural activity and distance from the potential OCP emitters have important influences on the OCP residue distributions. Principal component analysis indicates that HCH pollution is a mix of historical technical HCH and current lindane pollution and DDT pollution input is only due to technical DDT sources. The significant correlations of OCP compounds reveal that HCHs, DDTs and HCB could have some similar sources of origin.     

Polybrominated diphenyl ethers and organochlorine pesticides in human breast milk from Massachusetts, USA

Concentrations of polybrominated diphenyl ethers (PBDEs), and organochlorine pesticides (OCPs; DDTs, HCHs, CHLs, and HCB) were measured in human breast milk samples collected across Massachusetts, USA, in 2004. Seventeen PBDE congeners were found in the samples, ranging in concentration from 0.06 to 1910 ng g(-1) lipid wt. BDE-47 (2,2',4,4'-tetraBDE), BDE-99 (2,2',4,4',5-pentaBDE), and BDE-100 (2,2',4,4',6-pentaBDE) were the major congeners detected in breast milk samples. Overall mean (+/-SD) concentrations of DDTs, HCHs, CHLs, and HCB were 64.5 +/- 75, 18.9 +/- 19, 32.4 +/- 36, and 2.3 +/- 2.2 ng g(-1) lipid wt, respectively. Concentrations of PBDEs were strongly correlated with concentrations of OCPs in the samples. Based on the concentrations of organohalogens and the intake rates of breast milk by infants in the United States, daily ingestion rates of contaminants were calculated. The median ingestion rates for PBDEs, HCHs, DDTs, CHLs, and HCB were 4.0, 212, 141, 44, and 5.79 ng kg(-1) body wt day(-1), respectively. The estimated daily intake of organohalogens by infants was compared with threshold reference values suggested by the United States Environmental Protection Agency (USEPA) and the Agency for Toxic Substances and Disease Registry (ATSDR), for calculation of hazard quotients (HQs). HQs for individual organohalogens and the sum of HQ for all organohalogens were calculated as HQ indices (HQI). The results suggest that one or more of the contaminants analyzed in this study exceeded the threshold reference values in at least 26% of the breast milk samples.     

Organochlorine pesticide residues in Songkla Lake

The water quality of Songkla Lake for organochlorine (OC) pesticide contamination was studied from chosen sampling sites (stations) using the lakes geographic data and pollution sources. The water samples were collected monthly from 13 stations in Songkla Lake during September 1991–November 1992. The OC pesticide residues found were Heptachlor, Heptachlor Epoxide, DDD, DDE, DDT and Aldrin in the range 0–0.5690 ppm. This study showed that DDT and its metabolite products (DDD and DDE) dominated OC pesticide residues in the lake. The concentration of OC residues also depended on the season, i.e. at some sampling stations the concentration of OC residues in the dry season (July–September) were higher than in the wet season (October–January).     

Distribution of Organochlorine Pesticides in the Chao Phraya River, Thailand

Water samples from the Chao Phraya River, the main river in Thailand were collected and analyzed during 1988–1994. Organochlorine pesticides such as HCHs, DDTs, aldrin, dieldrin and chlordanes were determined. Aldrin and dieldrin had high frequencies of occurrence in water samples. The concentration median of the pesticides was approximately one order of magnitude higher than those of total HCHs and DDTs. Levels of aldrin were relatively high in the upstream while levels of DDTs were high in the urban area of Bangkok during 1989–1990. p,p-DDE levels were relatively higher in 1992. No clear trends in the levels of pesticides were observed.     

Time course of organochlorine pesticides and polychlorinated biphenyls in breast-feeding mothers throughout the first 10 months of lactation in Tunisia

Organochorine (OCs) residues were measured in human breast milk samples from four Tunisian women. Month-mix samples composed of weekly collected breast milk samples were analyzed over the lactation period between 3 days after delivery and 10 months post-partum. The concentrations of dichlorodiphenytrichloroethane and its metabolites (DDTs), hexachlorobenzene (HCB), hexachlorocyclohexane isomers (HCHs), dieldrin, and 20 polychlorinated biphenyl congeners (PCBs) were determined by gas chromatography with electron capture detection. The variation of OC residue levels in human milk was investigated for each woman individually. The average p,p’-DDE and p,p’-DDT concentrations declined from 661- and 438-ng g^?1 fat basis at day 3 to 77- and 106-ng g^?1 fat basis after 8 months, respectively. No essential changes in HCB, HCHs, dieldrin, and total PCBs concentrations in human breast milk occurred over the lactation periods investigated; the concentrations remained either relatively constant or show no significant weak decrease.