Global S&T Development Trend Analysis Platform of Resources and Environment
DOI | 10.5194/acp-18-3485-2018 |
Temporally delineated sources of major chemical species in high Arctic snow | |
Macdonald, Katrina M.1; Sharma, Sangeeta2; Toom, Desiree2; Chivulescu, Alina2; Platt, Andrew2; Elsasser, Mike2; Huang, Lin2; Leaitch, Richard2; Chellman, Nathan3; McConnell, Joseph R.3; Bozem, Heiko4; Kunkel, Daniel4; Lei, Ying Duan1; Jeong, Cheol-Heon1; Abbatt, Jonathan P. D.5; Evans, Greg J.1 | |
2018-03-09 | |
发表期刊 | ATMOSPHERIC CHEMISTRY AND PHYSICS
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ISSN | 1680-7316 |
EISSN | 1680-7324 |
出版年 | 2018 |
卷号 | 18期号:5页码:3485-3503 |
文章类型 | Article |
语种 | 英语 |
国家 | Canada; USA; Germany |
英文摘要 | Long-range transport of aerosol from lower latitudes to the high Arctic may be a significant contributor to climate forcing in the Arctic. To identify the sources of key contaminants entering the Canadian High Arctic an intensive campaign of snow sampling was completed at Alert, Nunavut, from September 2014 to June 2015. Fresh snow samples collected every few days were analyzed for black carbon, major ions, and metals, and this rich data set provided an opportunity for a temporally refined source apportionment of snow composition via positive matrix factorization (PMF) in conjunction with FLEXPART (FLEXible PARTicle dispersion model) potential emission sensitivity analysis. Seven source factors were identified: sea salt, crustal metals, black carbon, carboxylic acids, nitrate, non-crustal metals, and sulfate. The sea salt and crustal factors showed good agreement with expected composition and primarily northern sources. High loadings of V and Se onto Factor 2, crustal metals, was consistent with expected elemental ratios, implying these metals were not primarily anthropogenic in origin. Factor 3, black carbon, was an acidic factor dominated by black carbon but with some sulfate contribution over the winter-haze season. The lack of K+ associated with this factor, a Eurasian source, and limited known forest fire events coincident with this factor's peak suggested a predominantly anthropogenic combustion source. Factor 4, carboxylic acids, was dominated by formate and acetate with a moderate correlation to available sunlight and an oceanic and North American source. A robust identification of this factor was not possible; however, atmospheric photochemical reactions, ocean microlayer reaction, and biomass burning were explored as potential contributors. Factor 5, nitrate, was an acidic factor dominated by NO3-, with a likely Eurasian source and mid-winter peak. The isolation of NO3- on a separate factor may reflect its complex atmospheric processing, though the associated source region suggests possibly anthropogenic precursors. Factor 6, non-crustal metals, showed heightened loadings of Sb, Pb, and As, and correlation with other metals traditionally associated with industrial activities. Similar to Factor 3 and 5, this factor appeared to be largely Eurasian in origin. Factor 7, sulfate, was dominated by SO24- and MS with a fall peak and high acidity. Coincident volcanic activity and northern source regions may suggest a processed SO2 source of this factor. |
领域 | 地球科学 |
收录类别 | SCI-E |
WOS记录号 | WOS:000427039600001 |
WOS关键词 | BLACK CARBON EMISSIONS ; LIGHT CARBOXYLIC-ACIDS ; AIR-POLLUTION ; METHANESULFONIC-ACID ; SOURCE APPORTIONMENT ; SOURCE ATTRIBUTION ; AEROSOL ; BIOMASS ; ATMOSPHERE ; GREENLAND |
WOS类目 | Environmental Sciences ; Meteorology & Atmospheric Sciences |
WOS研究方向 | Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://119.78.100.173/C666/handle/2XK7JSWQ/27326 |
专题 | 地球科学 |
作者单位 | 1.Univ Toronto, Dept Chem Engn & Appl Chem, Toronto, ON M5S 3E5, Canada; 2.Environm & Climate Change Canada, Climate Res Div, Toronto, ON M3H 5T4, Canada; 3.Desert Res Inst, Reno, NV 89512 USA; 4.Johannes Gutenberg Univ Mainz, Inst Atmospher Phys, Becher Weg 21, D-55128 Mainz, Germany; 5.Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada |
推荐引用方式 GB/T 7714 | Macdonald, Katrina M.,Sharma, Sangeeta,Toom, Desiree,et al. Temporally delineated sources of major chemical species in high Arctic snow[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2018,18(5):3485-3503. |
APA | Macdonald, Katrina M..,Sharma, Sangeeta.,Toom, Desiree.,Chivulescu, Alina.,Platt, Andrew.,...&Evans, Greg J..(2018).Temporally delineated sources of major chemical species in high Arctic snow.ATMOSPHERIC CHEMISTRY AND PHYSICS,18(5),3485-3503. |
MLA | Macdonald, Katrina M.,et al."Temporally delineated sources of major chemical species in high Arctic snow".ATMOSPHERIC CHEMISTRY AND PHYSICS 18.5(2018):3485-3503. |
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