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DOI 10.1016/j.scitotenv.2014.08.008

Медицинская библиотека · The Science of the total environment · 2014

Trends of ambient fine particles and major chemical components in the Pearl River Delta region: observation at a regional background site in fall and winter.

Fu Xiaoxin, Wang Xinming, Guo Hai, Cheung Kalam, Ding Xiang, Zhao Xiuying, He Quanfu, Gao Bo, Zhang Zhou, Liu Tengyu, Zhang Yanli

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: In the fall and winter of 2007 to 2011, 167 24-h quartz filter-based fine particle (PM2.5) samples were collected at a regional background site in the central Pearl River Delta. The PM2.5 showed an annual reduction trend with a rate of 8.58 μg m(-3) (p<0.01). The OC component of the PM2.5 reduced by 1.10 μg m(-3) yr(-1) (p<0.01), while the reduction rates of sulfur dioxide (SO2) and sulfate (SO4(2-)) were 10.2 μg m(-3) yr(-1) (p<0.01) and 1.72 μg m(-3) yr(-1) (p<0.01), respectively. In contrast, nitrogen oxides (NOx) and nitrate (NO(3-)) presented growth trends with rates of 6.73 μg m(-3) yr(-1) (p<0.05) and 0.79 μg m(-3) yr(-1) (p<0.05), respectively. The PM2.5 reduction was mainly related to the decrease of primary OC and SO4(2-), and the enhanced conversion efficiency of SO2 to SO4(2-) was related to an increase in the atmospheric oxidizing capacity and a decrease in aerosol acidity. The discrepancy between the annual trends of NOx and NO3(-) was attributable to the small proportion of NO3(-) in the total nitrogen budget.

CAPSULE ABSTRACT: Understanding annual variations of PM2.5 and its chemical composition is crucial in enabling policymakers to formulate and implement control strategies on particulate pollution.

Для цитирования: Fu Xiaoxin, Wang Xinming, Guo Hai, Cheung Kalam, Ding Xiang, Zhao Xiuying, He Quanfu, Gao Bo, Zhang Zhou, Liu Tengyu, Zhang Yanli. Trends of ambient fine particles and major chemical components in the Pearl River Delta region: observation at a regional background site in fall and winter.. The Science of the total environment. 2014. DOI: 10.1016/j.scitotenv.2014.08.008.

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