沉积(地质)
微粒
环境科学
空气质量指数
空气污染
中国
二氧化硫
污染
生态系统
旱季
酸雨
大气科学
季节性
水文学(农业)
环境化学
气候学
自然地理学
地理
气象学
化学
生态学
构造盆地
地质学
生物
考古
岩土工程
古生物学
地图学
作者
Xiaosheng Luo,Yuepeng Pan,K. W. T. Goulding,Lin Zhang,Xuejun Liu,Fusuo Zhang
标识
DOI:10.1016/j.atmosenv.2016.07.038
摘要
The large emissions of sulfur dioxide (SO 2 ) in China have raised worldwide concerns due to its contribution to acid rain and particulate pollution. Monitoring sulfur (S) concentrations and estimating its deposition are important for evaluating air quality and its effects on ecosystems and human health. To date atmospheric dry S deposition in China remains unclear due to the paucity of measurements, especially in rural regions where the ecosystems are sensitive to acid deposition. In this study, we monitored both SO 2 and particulate SO 4 2− (pSO 4 2− ) concentrations at 8 sites south and 8 sites north of the Huai River in rural and suburban parts of China between 2010 and 2012. The measured concentration of SO 2 and pSO 4 2− were combined with GEOS-Chem modeled dry deposition velocities to estimate dry S deposition inputs to the surfaces. SO 2 and pSO 4 2− concentrations were high from October/November to next March/April and they (esp. SO 2 ) decreased sharply since March/April at the northern sites, reflecting elevated SO 2 emissions by winter heating (which normally starts in October/November and ends in March/April in the north of the Huai River). However the southern sites did not show this trend. Annual dry deposition of SO 2 plus pSO 4 2− in this study ranged from 3.1 to 27.1 kg S ha −1 across all the sites in the year 2011 (except one site from May 2011 to April 2012) and showed large spatial variation. The sites in northern China had greater dry deposition due to the higher S concentrations compared with sites in southern China. We also found relatively low pSO 4 2− /pNO 3 - ratios at most sites, reflecting NO x emissions had a larger influence than SO 2 emissions on particle composition during the 2010–2012 period at the measurement sites. Our results suggest that dry S deposition is still important input to ecosystems in spite of slow reduction of Chinese national SO 2 emissions since 2005. More research on both wet and dry S deposition and their impacts on the environment and human health should be carried out following the introduction of policies to reduce SO 2 emissions. • Sulfur (S) dry deposition was quantified at eight southern and eight northern sites in China. • Total SO 2 plus pSO 4 2− deposition (3.1–27.1 kg S ha −1 yr −1 ) showed large spatial variation across all sites. • Concentration and dry deposition of S were remarkably higher at northern than southern sites. • Low pSO 4 2− /pNO 3 - ratios at most sites reflected increasing NO x relative to SO 2 emissions.
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