Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10111039 | Science of The Total Environment | 2005 | 17 Pages |
Abstract
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 μm) melted snow indicate that most samples are consistent with a diluted seawater composition. Deviations from this behaviour indicate additional SO42â and Clâ relative to seawater, suggesting a minor contribution from (probably local) coal combustion emissions (Alaska, Finland, Sweden, Svalbard). The samples with the highest Na and Clâ content (Canada, Russia) also have higher Na/SO42â and Clâ/SO42â 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 SO42â (NSS), suggesting that acidification due to long-range transport of SO2 pollution is not operating on an arctic-wide scale. In a few samples (Alaska, Finland, Sweden, Svalbard), a significant proportion (>50%) of SO42â is non-marine in origin. Sources for this non-marine SO42â 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 NO3â.
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Authors
Patrice de Caritat, Gwendy Hall, Sigurdur GıÌslason, William Belsey, Marlene Braun, Natalia I. Goloubeva, Hans Kristian Olsen, Jon Ove Scheie, Judy E. Vaive,