Chemical compositions of fog and precipitation at Sejila Mountain in the southeast Tibetan Plateau, China

被引:36
作者
Wang, Wei [1 ,2 ,3 ]
Xu, Wen [1 ]
Collett, Jeffrey L., Jr. [4 ]
Liu, Duanyang [5 ]
Zheng, Aihua [6 ]
Dore, Anthony J. [7 ]
Liu, Xuejun [1 ]
机构
[1] China Agr Univ, Coll Resources & Environm Sci, Natl Acad Agr Green Dev, Key Lab Plant Soil Interact MOE, Beijing 100193, Peoples R China
[2] Xizang Agr & Anim Husb Coll, Nyingchi 860000, Tibet, Peoples R China
[3] Xizang Agr & Anim Husb Coll, Minist Educ, Key Lab Forest Ecol Tibet, Nyingchi 860000, Tibet, Peoples R China
[4] Colorado State Univ, Dept Atmospher Sci, Ft Collins, CO 80523 USA
[5] China Meteorol Adm, Key Lab Transportat Meteorol, Nanjing 210008, Peoples R China
[6] Beijing Normal Univ, Anal & Testing Ctr, Beijing 100875, Peoples R China
[7] Ctr Ecol & Hydrol, Bush Estate, Penicuik EH26 0QB, Midlothian, Scotland
基金
中国博士后科学基金; 英国自然环境研究理事会; 中国国家自然科学基金;
关键词
Fog water; Ion concentration; Trace elements; Emission source; Southeast Tibet; CLOUD-WATER CHEMISTRY; NAM CO REGION; WET DEPOSITION; INTERCEPTED CLOUDS; INORGANIC NITROGEN; FOREST ECOSYSTEMS; SIZE-DEPENDENCE; AQUEOUS-PHASE; RAIN-FOREST; AEROSOL;
D O I
10.1016/j.envpol.2019.07.055
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Chemical compositions of fog and rain water were measured between July 2017 and September 2018 at Sejila Mountain, southeast Tibet, where fog events frequently occurred in original fir forests at altitude 3950 m. Fog water samples were collected using a Caltech Active Strand Cloud Collector (CASCC), and rain samples were collected using a precipitation gauge. Differences were observed between fog water and rain composition for most analyzed ions. Ion abundance in fog water was Ca2+ > Cl- > Na+ > SO42- > Mg2+> NH4+ >K+ > NO3- whereas an order of Ca2+ > Na+ > Cl- > Mg2+ > SO42-> NO3- > K+> NH4+ was observed for rain water. All ion concentrations were higher in fog water than in rain water. Additionally, Ca2+ was the dominant cation in both fog and rain samples, accounting for more than half of all measured cations. NH4+ and SO42- concentrations were notable for being higher in fog than rain water when compared with other ions. For trace elements, Al, As, Mn and Se were the most abundant elements in fog water; only Al and As were detected in rain water. Seventy-two hour back-trajectory analysis showed that air masses during fog and/or rain events mainly came from the south of Sejila Mountain. Spearman correlation analysis and source contribution calculations indicated that both marine and terrestrial sources contributed to the observed ion concentrations. Considering the higher concentrations of NH4+ and higher ratio of NH4+/NO3- measured in fog than in rain, we suggest that quantification of fog nitrogen deposition and its ecological effect in this area should be given more attention. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:560 / 568
页数:9
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