Kan Ke-Cong, Gu Xiao-Hong, Li Hong-Min, Chen Hui-Hui, Mao Zhi-Gang, Zeng Qing-Fei
State Key Laboratory of Lake Science and Environment, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences, Nanjing 210008, China.
Huan Jing Ke Xue. 2020 Mar 8;41(3):1346-1356. doi: 10.13227/j.hjkx.201909043.
To investigate the distribution, source, and ecological risk of organochlorine pesticides (OCPs) residues in Lake Gucheng, surface water, sediment, and biological samples were collected from 12 sampling sites of Lake Gucheng and its inlets and outlets during summer and winter, and the concentrations of 19 OCPs were analyzed. The results showed that the concentration (dry weight) of OCPs in Lake Gucheng ranged from 26.74 to 48.12 ng·L in surface water, 9.01 to 35.34 ng·g in sediment, and 13.39 to 124.29 ng·g in organisms. The pollution characteristics of OCPs in surface water showed that the concentration was much higher in summer than in winter, and much higher at inflow and outflow rivers than in farming ponds and the central region of Lake Gucheng; the seasonal pollution characteristics in sediment were not obvious. All 19 kinds of OCPs in water, sediment, and organisms were detected in different degrees, and the dominant contaminants were HCHs and DDTs. -HCH was the main pollutant at all sites in both surface water and sediment, with 21% to 42% of total HCHs in two seasons. '-DDD was the main pollutant in surface water with 30% to 76% of total DDTs, whereas '-DDT was the main pollutant in sediment with 68% to 93% of total DDTs in two seasons. Source analysis based on ratios of HCHs isomers and DDTs isomers indicated that there was a new input of OCPs under anaerobic conditions in the study area. The ecological risk assessment showed that the OCPs in surface water did not lead to significant health risks, but the OCPs in sediments might pose ecological risks to the Lake Gucheng ecosystem. The organisms were within the acceptable potential carcinogenic risk range.
为调查固城湖有机氯农药(OCPs)残留的分布、来源及生态风险,于夏季和冬季从固城湖及其入水口和出水口的12个采样点采集了地表水、沉积物和生物样品,并分析了19种OCPs的浓度。结果表明,固城湖OCPs浓度(干重)在地表水中为26.74至48.12 ng·L,沉积物中为9.01至35.34 ng·g,生物体中为13.39至124.29 ng·g。地表水中OCPs的污染特征表明,夏季浓度远高于冬季,且在入流和出流河流处远高于养殖池塘和固城湖中心区域;沉积物中的季节性污染特征不明显。水、沉积物和生物体中均不同程度地检测到了所有19种OCPs,主要污染物为六六六(HCHs)和滴滴涕(DDTs)。α-HCH是地表水和沉积物中所有采样点的主要污染物,在两个季节中占总六六六的21%至42%。β-DDD是地表水中的主要污染物,占总滴滴涕的30%至76%,而β-DDT是沉积物中的主要污染物,在两个季节中占总滴滴涕的68%至93%。基于六六六异构体和滴滴涕异构体比例的源分析表明,研究区域在厌氧条件下有新的OCPs输入。生态风险评估表明,地表水中的OCPs不会导致显著的健康风险,但沉积物中的OCPs可能对固城湖生态系统构成生态风险。生物体处于可接受的潜在致癌风险范围内。