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条子河中多环芳烃和有机氯农药的时空分布及来源解析
引用本文:苏禹龙,徐晓萌,郭志勇,梁大鹏,花修艺,董德明.条子河中多环芳烃和有机氯农药的时空分布及来源解析[J].吉林大学学报(理学版),2014,52(3):611-622.
作者姓名:苏禹龙  徐晓萌  郭志勇  梁大鹏  花修艺  董德明
作者单位:吉林大学 地下水资源与环境教育部重点实验室, 水资源与水环境吉林省重点实验室, 环境与资源学院, 长春 130012
基金项目:国家“水体污染控制与治理科技重大专项”基金(批准号:2012ZX07202-009);教育部博士学科点专项科研基金(批准号:20100061110041);吉林省环境保护厅项目(批准号:吉环科字第2010-14号)
摘    要:以辽河支流条子河中的多环芳烃(PAHs)和有机氯农药(OCPs)为目标物,分别于春汛期、丰水期、平水期和枯水期采集水样及表层沉积物样品,分析样品中PAHs和OCPs的赋存状态及污染物在该区域的分布和来源.结果表明:条子河水中总PAHs的质量浓度为658.1~3 096.6ng/L,均值(算术平均值,下同)为1 522.1ng/L;沉积物中总PAHs的质量比为775.7~2 835.4ng/g,均值为1 374.0ng/g;条子河水中总α,β,γ-HCHs(六六六)的质量浓度为5.36~16.57ng/L,均值为10.93ng/L;滴滴涕(DDTs)未检出;沉积物中总HCHs的质量比为2.87~5.56ng/g,均值为4.34ng/g;条子河水和沉积物中PAHs的含量均为自上游至下游递减,且枯水期平水期春汛期丰水期;条子河水中HCHs的质量浓度自上游至下游递增,且丰水期春汛期平水期枯水期,沉积物中HCHs的质量比自上游至下游递减,且枯水期平水期春汛期丰水期;条子河中的PAHs主要来源于煤炭燃烧和交通燃烧,HCHs主要来源于农药林丹的使用.

关 键 词:条子河  多环芳烃  有机氯农药  时空分布  源解析  
收稿时间:2013-10-10

Temporospatial Distribution and Source Identification of PolycyclicAromatic Hydrocarbons and Organochlorine Pesticides in Tiaozi River
SU Yulong,XU Xiaomeng,GUO Zhiyong,LIANG Dapeng,HUA Xiuyi,DONG Deming.Temporospatial Distribution and Source Identification of PolycyclicAromatic Hydrocarbons and Organochlorine Pesticides in Tiaozi River[J].Journal of Jilin University: Sci Ed,2014,52(3):611-622.
Authors:SU Yulong  XU Xiaomeng  GUO Zhiyong  LIANG Dapeng  HUA Xiuyi  DONG Deming
Institution:Key Lab of Groundwater Resources and Environment of Ministry of Education,Key Lab of Water Resources and  Aquatic Environment of Jilin Province,College of Environment and Resources, Jilin University, Changchun 130012, China
Abstract:Water and surface sediment samples were collected from the Tiaozi River, a branch of Liaohe River, in spring, summer, autumn and winter to determine the contents of polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs). On this basis, the distribution and sources of the two organic pollutants were investigated. Results indicate that the total PAHs levels in the water samples were 658.1—3 096.6 ng/L (arithmetic mean: 1 522.1 ng/L) and those in the sediments were 775.7—2 835.4 ng/g (1 374.0 ng/g). α,β,γ Hexachlorocyclohexanes (HCHs) were detected in all the samples and the total HCHs were 5.36—16.57 ng/L (10.93 ng/L) in the water samples and 2.87—5.56 ng/g (4.34 ng/g) in the sediments. Dichlorodiphenyl trichloroethanes (DDTs) in all the samples were below the detection limit. Temporospatial distributions of PAHs in the river water and sediments were similar: the PAHs levels decreased in the order of winter>autumn>spring>summer and decreased from the upstream to the downstream. In contrast, temporospatial distributions of HCHs in the river water and sediments were opposite: HCHs levels in the water decreased in the order of summer>spring>autumn>winter and reduced from the downstream to the upstream; HCHs levels in the sediments decreased in the order: winter>autumn>spring>summer and decreased from the upstream to the downstream. The results for source identification of PAHs and HCHs reveal that PAHs in the river were mainly from the combustion of coal and transportation, and HCHs were from the past use of lindane.
Keywords:Tiaozi River  polycyclic aromatic hydrocarbon (PAHs)  organochlorine pesticide (OCPs)  temporospatial distribution  source identification
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