Peng Ke-Xing, Li Rui-Fei, Zhou Yi-Chen, Zhuo Ze-Ming, Zhang Jin, Li Mei, Li Xue
Institute of Mass Spectrometry and Atmospheric Environment, Jinan University, Guangzhou 510632, China.
Institute of Urban and Industrial Water Management, Technische Universität Dresden, Dresden 01062, Germany.
Huan Jing Ke Xue. 2022 Jul 8;43(7):3645-3655. doi: 10.13227/j.hjkx.202109272.
Polycyclic aromatic hydrocarbons (PAHs) are a type of typical environmental pollutant with carcinogenic effects and high ecological risk. With the development of industry, surface water acts as a primary sink for PAHs. Owing to their low solubility, a significant amount of PAHs are adsorbed onto suspended particulate matter in surface water, which presents a serious risk to human health and the ecological environment. To protect human health and aquatic organisms, a systematic assessment of the trends in PAHs exposure risk is essential. Based on long-term monitoring data from 2002 to 2016, this study systematically evaluated the spatiotemporal distribution and source apportionment of PAHs adsorbed on suspended particulate matter in surface water. The results of the Mann-Kendall test indicated that pollution levels of PAHs decreased from 2012 to 2016. The maximum average content was 6239 μg·kg, and the minimum was 2760 μg·kg. Benzo(b)fluoranthene, benzo(k)fluoranthene, chrysene, and benzo(a)anthracene showed significant declines from 2002-2016 (<0.05). Levels of benzo(a)pyrene, dibenzo(a,h)anthracene, and indeno(1,2,3-cd)pyrene were steady. Wavelet analysis showed that the pollution level of PAHs had significant periodic oscillations for surface water. Midstream and downstream ΣPAHs showed significant declines from 2002-2016 (<0.05), whereas upstream ΣPAHs were steady. ANOVA analysis showed that the spatial difference was significant and occurred in the following order:midstream (6168 μg·kg)>upstream (5407 μg·kg)>downstream (3412 μg·kg). Diagnostic ratio analysis and the positive matrix factorization model suggested that the major sources of PAHs were traffic sources, coal burning sources, and biomass combustion sources, which accounted for 40.9%, 33.7%, and 25.4%, respectively. The contribution of traffic sources decreased by 25.9%. The contributions of coal burning sources and biomass combustion sources increased by 4.8% and 21.1% from 2002-2009 to 2010-2016, respectively. These results provide scientific reference for risk analysis and the control of PAHs pollution in surface water.
多环芳烃(PAHs)是一类具有致癌作用和高生态风险的典型环境污染物。随着工业的发展,地表水成为PAHs的主要汇。由于其低溶解度,大量PAHs吸附在地表水中的悬浮颗粒物上,这对人类健康和生态环境构成严重风险。为保护人类健康和水生生物,系统评估PAHs暴露风险趋势至关重要。基于2002年至2016年的长期监测数据,本研究系统评估了地表水中吸附在悬浮颗粒物上的PAHs的时空分布和源解析。Mann-Kendall检验结果表明,2012年至2016年PAHs污染水平下降。最大平均含量为6239μg·kg,最小为2760μg·kg。苯并(b)荧蒽、苯并(k)荧蒽、芘和苯并(a)蒽在2002 - 2016年呈显著下降(<0.05)。苯并(a)芘、二苯并(a,h)蒽和茚并(1,2,3-cd)芘水平稳定。小波分析表明,PAHs污染水平在地表水中具有显著的周期性振荡。2002 - 2016年,中游和下游ΣPAHs呈显著下降(<0.05),而上游ΣPAHs稳定。方差分析表明,空间差异显著,顺序如下:中游(6168μg·kg) > 上游(5407μg·kg) > 下游(3412μg·kg)。诊断比值分析和正定矩阵因子分解模型表明,PAHs的主要来源是交通源、燃煤源和生物质燃烧源,分别占40.9%、33.7%和25.4%。交通源贡献下降了25.9%。2002 - 2009年至2010 - 2016年,燃煤源和生物质燃烧源的贡献分别增加了4.8%和21.1%。这些结果为地表水PAHs污染的风险分析和控制提供了科学参考。