巢湖表层水体中有机氯农药的分布及其组成

以固相萃取-气相色谱法/电子捕获检测器(SPE-GC/ECD)作为检测手段,对巢湖表层水体中有机氯农药(OCPs)的分布及组成特征进行分析.结果表明:研究区13个采样点中共检出包括六六六(HCHs)、滴滴涕(DDTs)、β-硫丹(β-Endosulfan)、艾氏剂(Aldrin)、六氯苯(hexachlorobenzene)和七氯(Heptachlor)在内的16种有机氯农药,其总含量范围为0.54～64.01ng.L-1;16种有机氯农药中以HCHs和DDTs为主,其平均质量浓度分别为5.56ng.L-1和16.57ng.L-1,约占其总量的84.75%;研究区的有机氯农药污染除了主要源于历史上农田中有机氯农药的残留外,近期可能还有新的农药污染源进入水环境;研究区所检出的各类有机氯农药均未超过国家地表水环境质量标准,巢湖表层水体中有机氯农药含量及潜在风险均属于中等偏低水平.     

宁波滩涂贝类养殖区沉积物中有机氯农药和多氯联苯残留及生态风险评估

利用GC-ECD对宁波市主要滩涂贝类养殖区表层沉积物中的多氯联苯(PCBs)和有机氯农药六六六(HCHs)、滴滴涕(DDTs)的残留量进行测定,研究其分布状况,并进行生态风险评估.结果表明:贝类养殖区表层沉积物中的总有机氯农药含量为0.80～32.40ng·g-1,多氯联苯含量为3.20～33.33 ng·g-1.HCHs主要来自远距离大气传输及历史残留,部分区域有DDTs输入,其来源可能是三氯杀螨醇的使用.大部分站位的p,p’-DDT和DDTs存在潜在的生态风险,其中墙头和西店海域的p,p’-DDT残留超过生物效应中值,对底栖生物毒害效应较高.大多数站位PCBs的生态风险较低.     

有机氯农药在大滨鹬和红腹滨鹬体内的富集程度

为探讨东亚-澳大利西亚迁徙路线上的鸻鹬类体内有机氯农药的含量及来源,本研究以该迁徙路线上的大滨鹬(Calidris tenuirostris)和红腹滨鹬(C.canutus)为研究对象,用索氏提取法对这两种鸟的胸肌和皮下脂肪中的有机污染物进行萃取,并用气相色谱法对19种有机氯农药进行检测。结果表明,HCHs、DDTs、硫丹Ⅱ等14种有机氯农药在大滨鹬和红腹滨鹬的组织中均有不同程度的检出,所有样品中的含量最高值达1 573.5 ng/g脂重;在检出的14种有机氯农药中,α-HCH、β-HCH、γ-HCH、p,p′-DDE、硫丹Ⅱ、硫丹硫酸酯和/或p,p′-DDT的检出率达100%;在大滨鹬的肌肉组织、红腹滨鹬的肌肉和脂肪组织中,p,p′-DDE的残留量最高;而在大滨鹬的脂肪组织中硫丹硫酸酯和/或p,p′-DDT的含量最高;目标物中的艾氏剂、异狄氏剂、七氯、反式氯丹等未达检出限或含量较低。我们对比了不同物种及不同组织样本中有机氯农药的富集程度,红腹滨鹬的肌肉组织中HCHs的沉积量显著高于大滨鹬,而大滨鹬的脂肪组织中硫丹硫酸酯和/或p,p′-DDT的含量显著高于红腹滨鹬。此外,分别对比两个物种的肌肉组织和脂肪组织中有机氯农药沉积量,部分有机氯农药在脂肪组织中的沉积量显著高于肌肉组织,说明相比于肌肉组织,有机氯农药可能更易于在脂肪组织中累积。     

太湖湿地生态系统有机氯污染的夜鹭生物指示

1999年春季,在对无锡鼋头渚鹭鸟种群野外生态调查的基础上,对夜鹭幼鸟反吐物,觅食地底泥和水体进行了采样,并在实验室用气相色谱测定了样品中的α-HCH、β-HCH、γ-HCH、艾氏剂、狄氏剂、异狄氏剂、七氯、环氧七氯、p,p'-DDE、p,p'-DDD、o,p'-DDT和p,p'-DDT等有机氯农药的残留状况,结果表明,在有机氯农药禁用近20年后,六六六的异构体和滴滴涕及其衍生物均能在环境中和夜鹭食物中有不明,在有机氯农药禁用近20年后,六六六的异构体和滴滴涕及其衍生物均能在环境中和夜鹭食物中有不明,在有机氯农药禁用近20年后,六六六的异构体和滴滴涕及其衍生物均能在环境中和夜鹭食物中有不检出,有机氯污染物沿夜鹭食物链产生逐级富集,太湖湿地生态系统中夜鹭卵富集了滴滴涕万倍以上,富集了六六六数千倍,从而使有机氯污染物易被检测,因此夜鹭锘放可作为湿地生态系统有机氯污染的生物指示物。     

DDTs和HCHs在珠江口南部海域管角螺的组织分布及生物转化

通过测定珠江口海域典型腹足类管角螺(Hemifusus tuba)各组织器官中DDTs和HCHs的含量,研究了管角螺体内DDTs和HCHs的组织分布和生物转化规律.结果表明:管角螺肠中DDTs和HCHs含量远高于其他器官,表明其肠壁对有机氯农药有一定的屏蔽作用;性腺中检出较高浓度的DDTs和HCHs,表明性腺是DDTs...     

南亚热带典型地区农业土壤中多环芳烃和有机氯农药研究

参考美国EPA标准方法对南亚热带潮汕地区农业土壤中持久性有机污染物多环芳烃（PAHs）和有机氯农药（OCPs）进行分析,并对其分布和来源进行研究,最后探讨了不同种植方式下污染物的污染特征。结果表明：该区农业土壤中PAHs含量范围从22．1ng／g到1256．9ng／g,与其它地区的污染程度和一些土壤环境质量标准相比,该区处于中等污染水平。高温裂解是土壤PAHs的主要来源。OCPs在被禁止20a后在土壤中仍有残留,残留水平从4．6ng／g到1021．5ng／g,其中HCHs和DDTs的残留未超过国家土壤环境质量标准。早期使用残留是其主要污染源,但新近仍有DDT和硫丹的输入。PAHs和OCPs的污染主要集中在土壤表层和亚表层,且随着深度的加深,污染逐渐减少,但40cm以下,污染变化很小。菜地土壤PAHs污染水平低于稻田土壤,而OCPs污染水平高于稻田土壤。     

安徽农田表层土壤中有机氯农药的分布及其组成

以安徽省寿县等19个地区的农田表层土壤(0～20 cm)为对象,采用超声波提取,气相色谱法/电子捕获检测器(GC/ECD)检测,分析了α-六六六、β-六六六、γ-六六六、δ-六六六、op′-DDE、pp′-DDD、α-硫丹和百菌清等8种有机氯农药(OCPs)在农田表层土壤中的分布及组成特征.结果表明： 19个取样点中8种有机氯农药残留的总含量范围为ND～23.75 μg·kg^-1,其中PP′-DDD、γ-HCH为主要污染物,平均质量浓度分别为13.83和13.49 μg·kg^-1.与1990年的调查结果相比,六六六平均值含量呈明显下降趋势;与国内外土壤相比,安徽省农田表层土壤中的六六六(HCHs)处于中等偏高的水平.安徽省农田表层土壤中OCPs、HCHs和pp′-DDD平均浓度分别为48.58、28.64和13.83 μg·kg^-1,均未超过《土壤环境质量标准》(GB 15618-1995)的一级土壤质量标准(<50 μg·kg^-1),污染较轻.     

废弃工业场地有机氯农药分布及生态风险评价

对典型废弃有机氯农药生产场地中土壤中六六六（α-,β-,γ-,δ-HCH）和滴滴涕（p,p’-DDT,p,p′-DDE,p,p′-DDD,o,p’-DDT）的残留特征进行了分析。结果发现场地中六六六的残留水平为13.16～148.71mg/kg;滴滴涕残留水平为3.02～67.42mg/kg。表层土残留最大,随着土层加深,污染物残留逐渐下降。六六六的残留水平要高于滴滴涕。残留分析表明场地中有机氯农药有逐步降解的趋势,但是现有残留水平超出了国家的土壤质量二级标准。根据场地土地利用方向,运用CalTOX暴露模型结合Monte Carlo分析进行了健康风险评价,结果表明,健康风险主要来自于两种人体暴露途径：皮肤吸收和呼吸摄入,总的风险都超过了可接受风险水平（10^-6）,通过敏感性分析表明5个参数对于总的风险贡献较大。该研究对于有机氯农药场地土壤的风险管理提供了依据。     

厦门海域贝类养殖环境中有机氯农药的积累和降解

利用气相色谱法(GC-ECD)对厦门海域贝类养殖环境(海水、底质和养殖贝类)中有机氯农药六六六(HCH)和滴滴涕(DDT)的含量进行了调查分析,初步探讨了贝类养殖环境中HCH和DDT的积累和降解规律.结果表明:厦门海域不同种贝类养殖环境中HCH和DDT的积累和降解存在明显差异,主要与各种贝类的栖息环境和生理生活习性有关.贝类养殖环境中处于积累状态(Rx＞1)的主要为p-HCH、δ-HCH和γ-HCH;处于降解状态(Rx＜1)的主要为α-HCH.α-HCH/γ-HCH的比值≤1.0,贝类养殖环境中的HCH来源于工业品HCH和林丹,大部分HCH为长时间残留,但尚有少量林丹输入.贝类养殖区海水中DDT主要为好氧降解,底质中主要为厌氧降解.海水中的降解产物主要为DDE,(DDD+ DDE )/DDTs(p,p-DDE+p,p-DDD+o,p-DDT+p,p-DDT)的比值＜0.5;底质和养殖贝类体中的降解产物主要为DDD,(DDD+DDE)/DDTs的比值＞0.5,贝类养殖区底质和养殖贝类体中的DDT大部分已降解为DDD和DDE,海水中尚有少量新的DDT输入.贝类养殖环境中HCH异构体降解率的高低顺序存在一定差异,其在贝类养殖生态系中的迁移、转化过程发生了构象变化.     

松辽流域河流表层沉积物中有机氯农药的分布特征

利用气相色谱-电子捕获检测器(gas chromatography-electron capture detector,GC-ECD)对松辽流域重点污染河流22个表层沉积物样品的13种有机氯农药进行了分析.结果表明,大辽河流域有机氯农药含量为3.06～23.24 ng·g^-1,松花江流域为4.26～18.45 ng·g^-1.松辽流域沉积物中主要有机氯农药为六六六(HCH),松花江流域和大辽河流域表现出了不同的污染趋势.松花江沉积物中也有较高的滴滴涕(DDT)残留量.整个松辽流域都有较高含量的丙体六六六(γ-HCH),超过了其初始效应浓度,可能对该地区水生生物产生毒性效应.     

Pollution assessment of organochlorine pesticides in urban agricultural soils of Jilin City,China

The content, source, and pollution level of organochlorine pesticides (OCPs) in soils are necessary to assess potential risks to eco-environment and human health, and to target environment-friendly policies. A total of 50 surface soil samples were collected from urban vegetable fields of Jilin City and thirteen OCPs were analyzed. The concentrations were in the ranges of 3.16–48.35 ng·g^?1 for Dichloro-Diphenyl-Tricgloroethanes (DDTs, sum of o, p′-DDT, p, p′-DDT, p, p′-DDD, and p, p′-DDE), 4.37–44.77 ng·g^?1 for Hexachlorocyclohexanes (HCHs, sum of α-HCH, β-HCH, γ-HCH, and δ-HCH), 1.19–13.17 ng·g^?1 for Chlordanes (sum of heptachlor, t-chlordane, and c-chlordane), 0.24–2.60 ng·g^?1 for aldrin, and nd–3.43 ng·g^?1 for dieldrin, respectively. The different compositions indicated that the residues of DDTs and HCHs originated mainly from the historical application, while chlordanes were mostly from recent input. On the basis of soil quality standards of China and the Netherlands, DDTs and chlordanes in this study were categorized as light pollution, and HCHs were classified as no pollution for the majority of soil samples. There are a variety of OCPs residues in urban vegetable soils of Jilin City, but it is still safe and suitable for agricultural production.     

Characterization,ecological and health risks of DDTs and HCHs in water from a large shallow Chinese lake

The levels of dichloro diphenyl trichloroethanes (DDTs) and hexachlorocyolohexanes (HCHs) in water from Lake Chaohu were measured. The residues, possible sources and potential ecological and health risks of these compounds were analyzed. The results show that the contents of total DDTs and HCHs in the water varied from 1.52 to 21.79 and from 1.58 to 31.66 ng L^− 1, respectively, which were higher than those in other Chinese lakes. The main sources of HCHs and DDTs were lindane and technical DDT, respectively. The o,p′-DDT/p,p′-DDT ratios indicated the new illegal inputs of DDT in all studied inflow rivers and some lake areas. The MOS10 (margin of safety) values suggested that the Lake was facing a potential ecological risks from p,p′-DDT, whereas the risk of γ-HCH was small. Both carcinogenic and noncarcinogenic risks of DDTs and HCHs associated with the water use were very low.     

Occurrence,distribution and possible sources of organochlorine pesticides in peri-urban vegetable soils of Changchun,Northeast China

The characterizations of residue levels and sources of organochlorine pesticides (OCPs) in soils are necessary to evaluate the potential pollution and risks of OCPs to the ecosystems and human health. A total of 51 surface soil samples were collected from peri-urban vegetable fields of Changchun and 13 OCPs were analyzed to learn the composition, spatial distribution and sources. The concentrations were in the ranges of 0.94–107.8 ng g^?1 for DDTs, 0.89–98.3 ng g^?1 for HCHs, 0.22–18.20 ng g^?1 for Chlordanes, nd–4.49 ng g^?1 for aldrin and nd–9.66 ng g^?1 for dieldrin, respectively. The total OCPs concentrations ranged from 2.44 to 177.1 ng g^?1 and the higher residues were mainly distributed in northeast and southwest sites, as well as sites along the Yitong River. According to the concentrations and detection frequencies, DDTs and HCHs were the most dominant compounds. Compositional analysis and principal component analysis suggested that DDT, HCH and chlordane in most soil samples derived from historical application except the slight fresh introduction at some locations. There exist a variety of OCPs residues in peri-urban vegetable soils of Changchun, but it is still safe and suitable for agricultural production for the most part, and some specific locations with high OCPs residues ought to be a cause for concern.     

Ecological Risk Assessment of Organochlorine Pesticides in Surface Waters of Lake Taihu,China

The residues of organochlorine pesticides (OCPs) in surface waters from Meiliang Bay, Gonghu Bay, and Xukou Bay of Lake Taihu, China, were investigated, and their ecological risks were assessed using the risk quotient method and probabilistic risk assessment. Environmental concentrations of OCPs in surface water of these bays were relatively lower compared with other rivers or lakes in China. Calculation of risk quotient associated with taxonomic groups indicates moderate ecological risks from OCPs for crustaceans and insects in these bays, while the ecological risks were low for fish and negligible for phytoplankton. The ecological risk quotients associated with individual OCPs were lower than 0.01 in these bays, suggesting a negligible risk to aquatic organisms. Ecological risk from α-HCH was relatively lower compared with DDTs, endosulfans, and γ-HCH. The combined ecological risks were evaluated using probabilistic risk assessment for only eight OCPs owing to a lack of available toxicity data for β-HCH and δ-HCH. The percentage of species with the potential to be at risk from mixture of OCPs was lower than the criteria of 5% in each bay, indicating that the combined ecological risks were acceptable.     

Organochlorine Pesticides in Sediments around Chaohu Lake: Concentration Levels and Vertical Distribution

Eighteen organochlorine pesticides (OCPs) were investigated in surface sediments from the Nanfei River and in four sediment cores from the primary estuaries of Chaohu Lake, Eastern China. The results indicate that the OCP concentrations in the surface and core sediments around Chaohu Lake were 3.48–121.08 (with a mean of 34.93) ng/g and 0.60–39.28 (7.07) ng/g, respectively. Significantly higher concentrations of ΣOCPs were observed in sediment samples from the Nanfei River and its estuary. The three important OCP contributors around Chaohu Lake were dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexane isomers (HCHs), and hexachlorobenzene (HCB), which originated primarily from the historical use of technical DDTs and HCHs. A principal component analysis (PCA) suggests that HCB and lindane may originate from the same sources, and DDTs were greatly influenced by organic carbon from the soil environment and the impact of urbanization processes.     

Effect of Surfactant Tween 80 on the Anaerobic Degradation and Desorption of HCHs and DDX in Aged Soil under Saturated Condition with Low Liquid/Solid Ratio

The application of surfactant Tween 80 was investigated to accelerate the anaerobic degradation of HCHs (α-, β-, γ- and δ-hexachlorocyclohexane) and DDX (p,p′-DDT, o,p′-DDT, p,p′-DDE and p,p′-DDD) in aged soil from a former organochlorine pesticide manufacturing plant under saturated condition with low liquid/solid ratio (liquid/solid ratio = 0.50). The surfactant Tween 80 did not facilitate the degradation of HCHs and DDX in the soil used in this experiment. Subsequent desorption experiment results also showed that the surfactant Tween 80 did not increase the pollutant desorption from the soil. The results in this study are not in accordance with the results reported in previous literature. This difference might be due to the fact that the soils used in this experiment were polluted by HCHs and DDX for more than 20 years, and soil aging reduced the desorption of HCHs and DDX in soil. Furthermore, the surfactants might be adsorbed by soils in low liquid/solid ratio condition.     

Levels of Hexachlorocyclohexanes and Dichloro-Dipheny-Trichloroethanes in Penguin Droppings Collected from Ardley Island,Maritime Antarctic

This article reports the concentrations of hexachlorocyclohexanes (HCHs) and dichloro-diphenyl-trichloroethanes (DDTs) in fresh Gentoo penguin (Pygoscelis Papua) droppings deposited on the Ardley Island (62°13′S, 58°56′W), West Antarctica, and those in the island's two lake cores. In the fresh penguin droppings, metabolites were the predominant constituents of the DDT group, most likely due to the ban on DDT use in agriculture and the higher stability of the metabolites in the environment. In contrast, γ-HCH comprised 66% of the total HCHs, apparently due to the continuous use of Lindane in the Southern Hemisphere. The concentrations of HCHs and DDTs in the fresh droppings are many times higher than those in penguin plume, the latter currently being used as biomaterial for monitoring coastal contaminations in Antarctica. Results of this study indicate that penguin droppings have a good potential for use as another biomonitoring material in detecting the organochlorine pesticides and other contaminants in the maritime Antarctic. Because penguin droppings can be well preserved in lake sediments, they also provide a good and continuous historical record of these contaminants. The slight increase of DDTs since the 1990s, as observed in the aged penguin droppings in the sediment cores, suggests there have been new inputs of DDT into the Antarctic coastal ecosystem, probably from the illegal use of DDT in the Southern Hemisphere.