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城市化对中国沿海城市气态和颗粒态多环芳烃及多氯联苯的影响:水平、来源和健康风险。

Effects of urbanization on gaseous and particulate polycyclic aromatic hydrocarbons and polychlorinated biphenyls in a coastal city, China: levels, sources, and health risks.

机构信息

Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, People's Republic of China.

Ningbo Urban Environment Observation and Research Station-NUEORS, Chinese Academy of Sciences, Ningbo, 315800, People's Republic of China.

出版信息

Environ Sci Pollut Res Int. 2015 Oct;22(19):14919-31. doi: 10.1007/s11356-015-4616-2. Epub 2015 May 22.

Abstract

Gas/particle distributions of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) were measured in Xiamen from May 2009 to March 2010 to evaluate the impacts of urbanization on the fate of persistent organic pollutants (POPs) in the atmospheric environment. In a newly developing area (NDA), the concentrations of 16 PAHs (gas + particle) were significantly higher than that a historically urbanized area (HUA) (p value <0.05), while the trend of 28 PCBs was reversed. Diagnostic ratios and principle component analysis (PCA) implied that atmospheric PAHs in the NDA were mainly derived from petrogenic combustion, including mixed sources of vehicle emissions, biomass burning and oil combustion, while pyrogenic combustion (e.g., traffic and coal combustion) was considered the major source of PAHs in the HUA. Atmospheric PCBs in both HUA and NDA were dominated by TriCBs and PeCBs related to the use of commercial mixtures (Aroclors 1242 and 1254). Based on the toxicological equivalent factor (TEF) approach, total benzo[a]pyrene equivalent values in the HUA and NDA were 1.12 and 2.02 ng m(-3), respectively, exceeding the standard threshold values (1.0 ng m(-3)) of China and WHO. Average daily intake of dioxin-like compounds was 0.2 pg kg(-1) day(-1) in the HUA, which are below the WHO tolerable daily intake level. The results showed that the contribution to the toxic equivalency (TEQ) was dominated by PCB169, PCB105, and PCB81.

摘要

2009 年 5 月至 2010 年 3 月,在厦门采集大气气溶胶质谱,以评估城市化对大气环境中持久性有机污染物(POPs)归宿的影响。在一个新开发区域(NDA),16 种多环芳烃(气相+颗粒相)的浓度明显高于一个历史上已城市化区域(HUA)(p 值<0.05),而 28 种多氯联苯的趋势则相反。诊断比值和主成分分析(PCA)表明,NDA 大气中的多环芳烃主要来自于石油燃烧源,包括车辆排放、生物质燃烧和石油燃烧的混合源,而 HUA 中的多环芳烃则被认为主要来自于高温燃烧源(如交通和煤炭燃烧)。HUA 和 NDA 中的大气多氯联苯主要由三氯联苯和五氯联苯组成,与商用混合物(Aroclors 1242 和 1254)的使用有关。基于毒性等效因子(TEF)方法,HUA 和 NDA 中的总苯并[a]芘当量值分别为 1.12 和 2.02ngm(-3),超过了中国和世界卫生组织的标准阈值(1.0ngm(-3))。HUA 中的二噁英类化合物的日均摄入量为 0.2pgkg(-1)day(-1),低于世界卫生组织可耐受日摄入量水平。结果表明,对毒性等效(TEQ)的贡献主要来自于 PCB169、PCB105 和 PCB81。

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