Chemical composition of arctic snow:: concentration levels and regional distribution of major elements

被引:63
作者
de Caritat, P
Hall, G
Gìslason, S
Belsey, W
Braun, M
Goloubeva, NI
Olsen, HK
Scheie, JO
Vaive, JE
机构
[1] Geol Survey Norway, N-7491 Trondheim, Norway
[2] Geol Survey Canada, Ottawa, ON K1A 0E8, Canada
[3] Univ Iceland, Inst Sci, IS-107 Reykjavik, Iceland
[4] Leo Ussak Elementary Sch, Rankin Inlet, NT X0C 0G0, Canada
[5] Bur Land Management, No Dist Off, Fairbanks, AK 99709 USA
[6] Murmansk Marine Biol Inst, Murmansk, Russia
[7] Minerals Off, DK-3900 Nuuk, Greenland
[8] Sysselmannen Pa Svalbard, N-9170 Longyearbyen, Norway
关键词
snow chemistry; long-range transport; acidification; pollution; contamination;
D O I
10.1016/j.scitotenv.2004.05.031
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
At the end of the northern winter 1996/1997, 21 snow samples were collected from 17 arctic localities in Norway, Sweden, Finland, Svalbard, Russia, Alaska, Canada, Greenland and Iceland. Major element concentrations of the filtered (0.45 mum) melted snow indicate that most samples are consistent with a diluted seawater composition. Deviations from this behaviour indicate additional SO(4)(2-) and Cl(-) relative to seawater, suggesting a minor contribution from (probably local) coal combustion 4 emissions (Alaska, Finland, Sweden, Svalbard). The samples with the highest Na and Cl(-) content (Canada, Russia) also have higher Na/SO(4)(2-) and Cl(-)/SO(4)(2-) ratios than seawater, suggesting a slight contamination from (probably local) deicing activities. Local soil or rock dust inputs in the snow are indicated by 'excess' Ca contents (Alaska, Svalbard, Greenland, Sweden). No overall relationship was found between pH (range: 4.6-6.1) and total or non-seasalt SO(4)(2-) (NSS), suggesting that acidification due to long-range transport of SO(2) pollution is not operating on an arctic-wide scale. In a few samples (Alaska, Finland, of SO(4)(2-) Sweden, Svalbard), a significant proportion (>50%) of SO(4)(2-) is non-marine in origin. Sources for this non-marine SO(4)(2-) need not all be found in long-range atmospheric transport and more likely sources are local industry (Finland, Sweden), road traffic (Alaska) or minor snow-scooting traffic (one Svalbard locality). A few samples from northern Europe show a relatively weak trend of decreasing pH with increasing NO(3)(-) (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 199
页数:17
相关论文
共 43 条
[21]  
Hammer C. U., 1985, GEOPHYS MONOG SERIES, V33, P90, DOI [DOI 10.1029/GM033P0090/SUMMARY), 10.1029/GM033p0090]
[22]  
HANSSON ME, 1993, CHEM COMPOSITION INS
[23]  
HERRON MM, 1985, GEOPHYS MONOGR SER, V33, P77, DOI DOI 10.1029/GM033P0077
[25]  
Krachler M, 1996, FRESEN ENVIRON BULL, V5, P418
[26]   EXPLORATORY DATA-ANALYSIS - RECENT ADVANCES FOR THE INTERPRETATION OF GEOCHEMICAL DATA [J].
KURZL, H .
JOURNAL OF GEOCHEMICAL EXPLORATION, 1988, 30 (03) :309-322
[27]   Trace metal suites in Antarctic pre-industrial ice are consistent with emissions from quiescent degassing of volcanoes worldwide [J].
Matsumoto, A ;
Hinkley, TK .
EARTH AND PLANETARY SCIENCE LETTERS, 2001, 186 (01) :33-43
[28]  
Moller D., 1990, Tellus, Series B (Chemical and Physical Meteorology), V42B, P254, DOI 10.1034/j.1600-0889.1990.t01-1-00004.x
[29]   MULTIELEMENT REGIONAL GEOCHEMICAL RECONNAISSANCE AS AN AID TO TARGET SELECTION IN IRISH CALEDONIAN TERRAINS [J].
OCONNOR, PJ ;
REIMANN, C .
JOURNAL OF GEOCHEMICAL EXPLORATION, 1993, 47 (1-3) :63-87
[30]  
PFIFMAN S, 1994, CARC N PERSPECT, V21, P8