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High daytime abundance of primary organic aerosols over Mt. Emei, Southwest China in summer.
Zhao, Yue; Ren, Hong; Deng, Junjun; Li, Linjie; Hu, Wei; Ren, Lujie; Yue, Siyao; Fan, Yanbing; Wu, Libin; Li, Jie; Sun, Yele; Wang, Zifa; Akimoto, Hajime; Zeng, Xin; Cheng, Yi; Kong, Shaofei; Su, Hang; Cheng, Yafang; Kawamura, Kimitaka; Fu, Pingqing.
Afiliação
  • Zhao Y; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Ren H; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Deng J; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Li L; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
  • Hu W; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Ren L; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Yue S; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
  • Fan Y; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Wu L; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China.
  • Li J; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
  • Sun Y; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
  • Wang Z; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
  • Akimoto H; Center for Global Environmental Research, National Institute for Environmental Studies, Tsukuba, Japan.
  • Zeng X; Department of Atmospheric Science, School of Environmental Sciences, China University of Geosciences, Wuhan 430074, China.
  • Cheng Y; Department of Atmospheric Science, School of Environmental Sciences, China University of Geosciences, Wuhan 430074, China.
  • Kong S; Department of Atmospheric Science, School of Environmental Sciences, China University of Geosciences, Wuhan 430074, China.
  • Su H; Multiphase Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany.
  • Cheng Y; Multiphase Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany.
  • Kawamura K; Chubu Institute for Advanced Studies, Chubu University, Kasugai 487-8501, Japan.
  • Fu P; Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China. Electronic address: fupingqing@tju.edu.cn.
Sci Total Environ ; 703: 134475, 2020 Feb 10.
Article em En | MEDLINE | ID: mdl-31759721
ABSTRACT
Organic molecular composition of fine aerosols in the free troposphere is poorly understood. Here, PM2.5 (particles with aerodynamic diameters ≤ 2.5 µm) samples were collected at the summit of Mt. Emei (3080 m a.s.l.) in the Southwestern China on a daytime and nighttime basis during summer 2016 (June-July). The samples were analyzed by solvent-extraction followed by derivatization and gas chromatography/mass spectrometry (GC/MS). Four classes of organic compounds, i.e. n-alkanes, fatty acids, saccharides and lignin/resin acids were measured quantitatively. Fatty acids were found to be the most abundant species with an average concentration of 401 ±â€¯419 ng m-3 (range 25.7-1490 ng m-3) in the daytime, similar to the average concentration at night (399 ±â€¯447 ng m-3, 19.6-1970 ng m-3). However, the concentrations of biomass burning tracers (e.g., levoglucosan), primary biological aerosol tracers (e.g., mannitol and arabitol) and low molecular weight n-alkanes derived from fossil fuel combustion in daytime samples were obviously higher than those in nighttime samples. The results suggest that valley breezes transported a large number of aerosols and their precursors from the ground surface to the summit of Mt. Emei in the daytime. Estimated with tracer-based methods, the contributions of biogenic primary sources (plant debris, fungal spore, and biomass burning) to organic carbon was in the range of 3.28-83.5% (22.0 ±â€¯17.5%) in the daytime and 3.45-37.4% (10.9 ±â€¯8.97%) at night. As the largest contributor, biomass burning was an important anthropogenic/natural source of aerosol particles in the free troposphere over Mt. Emei. CAPSULE Valley/mountain breeze is an important constraint to the temporal variations in organic aerosols over Mt. Emei.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Total Environ Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China País de publicação: HOLANDA / HOLLAND / NETHERLANDS / NL / PAISES BAJOS / THE NETHERLANDS

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Total Environ Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China País de publicação: HOLANDA / HOLLAND / NETHERLANDS / NL / PAISES BAJOS / THE NETHERLANDS