Elemental and individual particle analysis of atmospheric aerosols from high Himalayas

被引:59
作者
Cong, Zhiyuan [1 ]
Kang, Shichang [1 ,2 ]
Dong, Shuping [3 ]
Liu, Xiande [4 ]
Qin, Dahe [2 ]
机构
[1] Chinese Acad Sci, Inst Tibetan Plateau Res, Beijing 100085, Peoples R China
[2] Chinese Acad Sci, State Key Lab Cryospher Sci, Lanzhou 730000, Peoples R China
[3] Natl Ctr Environm Anal & Measurements, Beijing 100029, Peoples R China
[4] Chinese Res Inst Environm Sci, Beijing 100012, Peoples R China
基金
中国国家自然科学基金;
关键词
Aerosols; Himalayas; Chemical composition; Individual particle analysis; SEM-EDX; CHEMICAL-COMPOSITION; CHEMISTRY; AIR; CLIMATE; POLLUTION; SULFATE; STATION; EVEREST; CITY; SNOW;
D O I
10.1007/s10661-008-0698-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atmospheric aerosols were collected during the scientific expedition to Mt. Qomolangma (Everest) in May-June, 2005. The elemental concentrations of the aerosols were determined by inductively coupled plasma mass spectrometry. This yielded data for the concentration of 14 elements: Na, Mg, Al, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, and Pb. The mean elemental concentrations were generally comparable with those from central Asia and the Arctic, while much higher than those from Antarctic. Size, morphology, and chemical composition of 900 individual aerosol particles were determined by scanning electron microscopy and energy-dispersive X-ray microanalysis. Based on morphology and elemental composition, the particles were clustered into eight groups: soot (8%), tar ball (3%), alumosilicates/silica (55%), calcium sulfate (16%), Ca/Mg carbonate (2%), Fe/Ti-rich particles (3%), Pb-rich particles (1%), and biological particles (12%). The sampling site, located at 6,520 m in the Himalayas, is particularly remote and located at high altitude. Nonetheless, high aerosol enrichment factors for copper, chromium, lead, nickel, vanadium, and zinc all suggest the influence of long-range transported pollution, while enrichment in calcium and the presence of alumino-silicates in individual particle analyses indicates a distinct mineral dust influence. The backward air mass trajectories showed that the northwestern part of India may contribute to the atmospheric aerosol in the central high Himalayas.
引用
收藏
页码:323 / 335
页数:13
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