School of Resources and Environmental Engineering, Hefei University of Technology, Hefei 246011, China.
National Institute of Environmental Health Sciences, National Health Research Institutes, 35 Keyan Road, Zhunan Town, Miaoli 35053, Taiwan.
Sci Total Environ. 2019 Jun 20;670:439-447. doi: 10.1016/j.scitotenv.2019.03.198. Epub 2019 Mar 15.
We investigated spatial and season variations in particle-bound PAH concentrations, identified their potential sources and estimated resultant health risk of activate toxicity pathways in a residential area near coal-fired power and steelmaking plants. Both atmospheric PM and PM samples (n = 94) were simultaneously collected for summer and winter in the Wuqi and Shalu districts of Taichung City, central Taiwan. The principal component analysis (PCA) measure was used to evaluate the sources of particle-bound PAHs. The health risk of PAHs-activated toxicity pathways was estimated through a probabilistic model in cooperation with high-throughput screening (HTS) in vitro assays and measurement data for children and adults. No spatial difference, but significant seasonal variation, in PAH concentrations for PM (summer = 1.7 ng m and winter = 4.7 ng m) and PM (summer = 2.1 ng m and winter = 4.8 ng m) between two sites was observed, where both sites shared the similar PAH patterns in congener concentrations. PAH contents in the fine mode (PM) of ambient particles are predominant while coarse mode (PM) PAHs is negligible. Children with particle-bound PAH exposures have a relatively high health risk of aryl hydrocarbon receptor (AhR)-mediated adverse outcomes than adults, in particular in the winter period, while the activations of Nrf2 and p53 pathways are insignificant. Vehicle emission (67.1%), unburned petroleum (15.0%), steel industry and stationary emission (6.1%), and oil combustion + cooking oil fume (5.6%) associated with PM-bound PAHs were apportioned. The emission from the Taichung coal-fired power plant is rarely attributable to particle-bound PAHs of the study area based on results of spatiotemporal variation of PAHs, wind direction, and source apportionment.
我们研究了燃煤电厂和钢铁厂附近居民区颗粒结合态多环芳烃(PAH)浓度的时空变化,识别了其潜在来源,并评估了活性毒性途径对健康的潜在风险。本研究于 2017 年夏冬两季在台湾中部台中市乌日区和沙鹿区同步采集大气颗粒物(PM)和细颗粒物(PM)样本(n=94)。主成分分析(PCA)用于评估颗粒结合态多环芳烃的来源。通过高通量筛选(HTS)体外测定和儿童及成人的实测数据,采用概率模型评估了多环芳烃活性毒性途径的健康风险。两个采样点的 PM(夏季=1.7ngm,冬季=4.7ngm)和 PM(夏季=2.1ngm,冬季=4.8ngm)中 PAH 浓度无空间差异,但有显著的季节变化,两个采样点的 PAH 模式相似,且细颗粒(PM)中的 PAH 含量占主导地位,粗颗粒(PM)中的 PAH 可忽略不计。与成人相比,儿童对颗粒结合态 PAH 的暴露有较高的健康风险,特别是在冬季,这与芳基烃受体(AhR)介导的不良后果有关,而 Nrf2 和 p53 途径的激活则不显著。与 PM 结合态 PAHs 相关的主要排放源有:机动车排放(67.1%)、未燃烧石油(15.0%)、钢铁工业和固定源排放(6.1%)以及油燃烧+食用油油烟(5.6%)。根据多环芳烃的时空变化、风向和源解析结果,台中燃煤电厂的排放对研究区域颗粒结合态 PAHs 的贡献可以忽略不计。