Geochemical, isotopic, and mineralogical constraints on atmospheric deposition in the hyper-arid Atacama Desert, Chile

被引:39
|
作者
Wang, Fan [1 ]
Michalski, Greg [1 ]
Seo, Ji-hye [2 ]
Ge, Wensheng [3 ]
机构
[1] Purdue Univ, Dept Earth Atmospher & Planetary Sci, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[3] China Univ Geosci, Sch Earth Sci & Resources, Beijing, Peoples R China
基金
美国国家科学基金会;
关键词
MARINE BOUNDARY-LAYER; SEA-SALT PARTICLES; NORTHERN CHILE; PEDOGENIC PROCESSES; CHEMICAL PROCESSES; NITROGEN ISOTOPES; AEROSOL-PARTICLES; SULFUR-DIOXIDE; DRY DEPOSITION; EXCESS SULFATE;
D O I
10.1016/j.gca.2014.03.017
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Modern atmospheric deposition across the Atacama was collected by an array of dust traps that stretched from the Pacific coast to the Andean altiplano, and the material was analyzed for its geochemical, mass and isotopic composition. The coastal trap had the second-highest insoluble mineral particle and highest soluble salt deposition rates due to significant inputs from the Morro Mejillones Range and the Pacific Ocean, respectively. The Andean trap had the highest insoluble mineral particle deposition owing to transport of weathered material, but the lowest deposition rate of soluble salts due to its distance from the ocean and anthropogenic sources. The removal of oceanic material was effective by the coastal mountains, while the westward transport of the Andean material was determined to be minimal. The atmospheric deposition in the inland traps was mainly from the local entrainment of surface material, inland anthropogenic emissions, and transport of marine aerosols. The nitrate isotopes (delta N-15 and Delta O-17) suggested that NOx sources and NO3- chemistry shifted along the west-east transect, and were greatly impacted by anthropogenic emissions with soil NO3- being a minor source of deposited nitrogen. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 48
页数:20
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