| 1. |
- Björkman, Mats P., et al.
(författare)
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Nitrate dry deposition in svalbard
- 2013
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 65, s. 19071-
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Tidskriftsartikel (refereegranskat)abstract
- Arctic regions are generally nutrient limited, receiving an extensive part of their bio-available nitrogen from the deposition of atmospheric reactive nitrogen. Reactive nitrogen oxides, as nitric acid (HNO3) and nitrate aerosols (p-NO3), can either be washed out from the atmosphere by precipitation or dry deposited, dissolving to nitrate (NO3-). During winter, NO3- is accumulated in the snowpack and released as a pulse during spring melt. Quantification of NO3- deposition is essential to assess impacts on Arctic terrestrial ecology and for ice core interpretations. However, the individual importance of wet and dry deposition is poorly quantified in the high Arctic regions where in-situ measurements are demanding. In this study, three different methods are employed to quantify NO3- dry deposition around the atmospheric and ecosystem monitoring site, Ny-Alesund, Svalbard, for the winter season (September 2009 to May 2010): (1) A snow tray sampling approach indicates a dry deposition of -10.27 +/- 3.84 mg m(-2) (+/- S.E.); (2) A glacial sampling approach yielded somewhat higher values -30.68 +/- 12.00 mg m(-2); and (3) Dry deposition was also modelled for HNO3 and p-NO3 using atmospheric concentrations and stability observations, resulting in a total combined nitrate dry deposition of -10.76 +/- 1.26 mg m(-2). The model indicates that deposition primarily occurs via HNO3 with only a minor contribution by p-NO3. Modelled median deposition velocities largely explain this difference: 0.63 cm s(-1) for HNO3 while p-NO3 was 0.0025 and 0.16 cm s(-1) for particle sizes 0.7 and 7 mm, respectively. Overall, the three methods are within two standard errors agreement, attributing an average 14% (total range of 2-44%) of the total nitrate deposition to dry deposition. Dry deposition events were identified in association with elevated atmospheric concentrations, corroborating recent studies that identified episodes of rapid pollution transport and deposition to the Arctic.
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| 2. |
- Björkman, Mats P., 1978, et al.
(författare)
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Nitrate postdeposition processes in Svalbard surface snow
- 2014
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Ingår i: Journal of Geophysical Research - Atmospheres. - 0148-0227 .- 2156-2202 .- 2169-897X .- 2169-8996. ; 119:22
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Tidskriftsartikel (refereegranskat)abstract
- The snowpack acts as a sink for atmospheric reactive nitrogen, but several postdeposition pathways have been reported to alter the concentration and isotopic composition of snow nitrate with implications for atmospheric boundary layer chemistry, ice core records, and terrestrial ecology following snow melt. Careful daily sampling of surface snow during winter (11-15 February 2010) and springtime (9 April to 5 May 2010) near Ny-Ålesund, Svalbard reveals a complex pattern of processes within the snowpack. Dry deposition was found to dominate over postdeposition losses, with a net nitrate deposition rate of (0.6+/-0.2) (my) molm 2 d 1 to homogeneous surface snow. At Ny-Ålesund, such surface dry deposition can either solely result from long-range atmospheric transport of oxidized nitrogen or include the redeposition of photolytic/bacterial emission originating from deeper snow layers. Our data further confirm that polar basin air masses bring 15 N-depleted nitrate to Svalbard, while high nitrate (delta) (18O) values only occur in connection with ozone-depleted air, and show that these signatures are reflected in the deposited nitrate. Such ozone-depleted air is attributed to active halogen chemistry in the air masses advected to the site. However, here the Ny-Ålesund surface snow was shown to have an active role in the halogen dynamics for this region, as indicated by declining bromide concentrations and increasing nitrate (delta) (18O), during high BrO (low-ozone) events. The data also indicate that the snowpack BrO-NO x cycling continued in postevent periods, when ambient ozone and BrO levels recovered.
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| 3. |
- Kuhnel, Rafael, et al.
(författare)
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Reactive nitrogen and sulphate wet deposition at Zeppelin Station, Ny-Alesund, Svalbard
- 2013
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Ingår i: Polar Research. - : Norwegian Polar Institute. - 0800-0395 .- 1751-8369. ; 32
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Tidskriftsartikel (refereegranskat)abstract
- As a potent fertilizer, reactive nitrogen plays an important role in Arctic ecosystems. Since the Arctic is a nutrient-limited environment, changes in nitrogen deposition can have severe impacts on local ecosystems. To quantify the amount of nitrogen deposited through snow and rain events, precipitation sampling was performed at Zeppelin Station, Svalbard, from November 2009 until May 2011. The samples were analysed for NO3-; nss-SO42- and NH4+ concentrations, and the deposition of single precipitation events was calculated using precipitation measurements taken at nearby Ny-Alesund. The majority of observed events showed concentrations ranging from 0.01 to 0.1 mg L-1 N for NO3- and NH4+ and from 0.02 to 0.3 mg L-1 S for nss-SO42-. The majority of calculated depositions ranged from 0.01 to 0.1 mg m(-2) N for NO3- and NH4+ and from 0.02 to 0.3 mg m(-2) S for nss-SO42-. The budget was controlled by strong deposition events, caused by long-lasting precipitation episodes that lasted for several days and which had raised concentrations of nitrogen and sulphur. Three future scenarios of increasing precipitation in the Arctic were considered. The results showed that deposition is mainly controlled by the amount of precipitation, which leads to the conclusion that increased precipitation might cause increases in deposition of the same magnitude.
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