Chemical characteristics of soluble aerosols over the central Himalayas: insights into spatiotemporal variations and sources

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作者
Lekhendra Tripathee
Shichang Kang
Dipesh Rupakheti
Zhiyuan Cong
Qianggong Zhang
Jie Huang
机构
[1] Northwest Institute of Eco-Environment and Resources,State Key Laboratory of Cryospheric Science
[2] Chinese Academy of Sciences,CAS Center for Excellence in Tibetan Plateau Earth Sciences
[3] Himalayan Environment Research Institute (HERI),Key Laboratory of Tibetan Environment Changes and Land Surface Processes
[4] Chinese Academy of Sciences,undefined
[5] Institute of Tibetan Plateau Research,undefined
[6] Chinese,undefined
[7] Academy of Sciences,undefined
关键词
Central Himalayas; Aerosol; Soluble inorganic ions; Spatial and temporal variations;
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摘要
In order to investigate the spatial and temporal variations of aerosols and its soluble chemical compositions of the data gap zone in the central Himalayan region, aerosol samples were collected at four sites. The sampling location were characterized by four different categories, such as urban (Bode), semi-urban site in the northern Indo-Gangetic Plain (Lumbini), rural (Dhunche), and semiarid rural (Jomsom). A total of 230 aerosol samples were collected from four representative sites for a yearlong period and analyzed for water-soluble inorganic ions (WSIIs). The annual average aerosol mass concentration followed the sequence as Bode (238.24 ± 162.24 μg/m3)> Lumbini (161.14 ± 105.95 μg/m3)> Dhunche (112.40 ± 40.30 μg/m3)> Jomsom (78.85 ± 34.28 μg/m3), suggesting heavier particulate pollution in the urban and semi-urban sites. The total soluble ions contributed to 12.61–28.19% of TSP aerosol mass. The results revealed that SO42− and NO3− were the major anion and Ca2+ and NH4+ were the major cation influencing the aerosol composition over the central Himalayas. Calcium played a major role in neutralizing aerosol acidity followed by NH4+ at all the sites. The major compound of aerosol was (NH4)2SO4 and NH4HSO4 in the central Himalayas. Clear seasonality was observed at three observation sites, with higher concentrations during non-monsoon (dry periods) and lower during monsoon (wet period), suggesting washing out of aerosol particles by heavy precipitation during monsoon. In contrast, semiarid sites did not show the clear seasonal trend due to limited precipitation. Stationary sources were predominant over the mobile sources mostly in the remote sites. Principal component analysis confirmed that the major sources of WSIIs in the region were industrial emissions, fossil fuel and biomass burning, and crustal fugitive dusts. Nevertheless, transboundary aerosol transport over the region from polluted cities from south Asia could not be ignored as indicated by the clusters of air mass backward trajectory analysis.
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页码:24454 / 24472
页数:18
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