Carmen P. Vega

Reactive nitrogen and sulphate wet deposition at Zeppelin Station, Ny-Alesund, Svalbard

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 , nss- and concentrations, and the deposition of single precipitation events was calculated using precipitation measurements taken at nearby Ny-Ålesund. The majority of observed events showed concentrations ranging from 0.01 to 0.1 mg L−1 N for and and from 0.02 to 0.3 mg L−1 S for nss- . The majority of calculated depositions ranged from 0.01 to 0.1 mg m−2 N for and and from 0.02 to 0.3 mg m−2 S for nss- . 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.

Nitrate postdeposition processes in Svalbard surface snow

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-Alesund, 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) μmol m A2 d A1 to homogeneous surface snow. At Ny-Alesund, 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 δ(18 O) 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-Alesund 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 δ(18 O), 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.

Nitrate stable isotopes and major ions in snow and ice samples from four Svalbard sites

Increasing reactive nitrogen (Nr) deposition in the Arctic may adversely impact N-limited ecosystems. To investigate atmospheric transport of Nr to Svalbard, Norwegian Arctic, snow and firn samples were collected from glaciers and analysed to define spatial and temporal variations (1–10 years) in major ion concentrations and the stable isotope composition (δ 15N and δ 18O) of nitrate ( ) across the archipelago. The and averaged −4‰ and 67‰ in seasonal snow (2010–11) and −9‰ and 74‰ in firn accumulated over the decade 2001–2011. East–west zonal gradients were observed across the archipelago for some major ions (non-sea salt sulphate and magnesium) and also for and in snow, which suggests a different origin for air masses arriving in different sectors of Svalbard. We propose that snowfall associated with long-distance air mass transport over the Arctic Ocean inherits relatively low due to in-transport N isotope fractionation. In contrast, faster air mass transport from the north-west Atlantic or northern Europe results in snowfall with higher because in-transport fractionation of N is then time-limited.

Nitrate and Sulfate Anthropogenic Trends in the 20th Century from Five Svalbard Ice Cores

Abstract Sulfate and nitrate records from 5 ice cores spread across Svalbard were compared and revealed strong temporal similarities with previously published global estimates of SO2 and NOx anthropogenic emissions during the 20th century. A significant departure from the early century sulfate and nitrate levels was evident at all drilling sites starting from the mid-1940s. A steady increase was observed in both sulfate and nitrate profiles at most sites until the late 1960s, when the annual concentrations started to increase at a higher rate. This peak activity lasted for about a decade, and was observed to decrease steadily from the early 1980s on, when sulfate levels declined significantly and when nitrate levels finally reached sulfate levels for the first time in 20th century. The timing of these trends in Svalbard with global SO2 and NOx concentration profiles was best appraised when considering composite concentration profiles of all Svalbard ice cores for sulfate and nitrate, respectively. Composite profiles were also found to provide a convenient mean for distinguishing between the most important world source regions. Based on correlation analysis, the major pollutant sources appeared to be Western Europe and North America for both sulfate and nitrate, followed by Central Europe and former U.S.S.R. in generally similar proportions.

First ice core records of NO3− stable isotopes from Lomonosovfonna, Svalbard

Samples from two ice cores drilled at Lomonosovfonna, Svalbard, covering the period 1957-2009, and 1650-1995, respectively, were analyzed for NO(3)(-)concentrations, and NO3- stable isotopes (N-15 ...

An 800 year high-resolution black carbon ice-core record from Lomonosovfonna, Svalbard

Produced by the incomplete combustion of fossil fuel and biomass, black carbon (BC) contributes to Arctic warming by reducing snow albedo and thus triggering a snow-albedo feedback leading to increased snowmelt. Therefore, it is of high importance to assess past BC emissions to better understand and constrain their role. However, only a few long-term BC records are available from the Arctic, mainly originating from Greenland ice cores. Here, we present the first long-term and high-resolution refractory black carbon (rBC) record from Svalbard, derived from the analysis of two ice cores drilled at the Lomonosovfonna ice field in 2009 (LF-09) and 2011 (LF-11) and covering 800 years of atmospheric emissions. Our results show that rBC concentrations strongly increased from 1860 on due to anthropogenic emissions and reached two maxima, at the end of the 19th century and in the middle of the 20th century. No increase in rBC concentrations during the last decades was observed, which is corroborated by atmospheric measurements elsewhere in the Arctic but contradicts a previous study from another ice core from Svalbard. While melting may affect BC concentrations during periods of high temperatures, rBC concentrations remain well preserved prior to the 20th century due to lower temperatures inducing little melt. Therefore, the preindustrial rBC record (before 1800), along with ammonium (NH+4 ), formate (HCOO ) and specific organic markers (vanillic acid, VA, and p-hydroxybenzoic acid, pHBA), was used as a proxy for biomass burning. Despite numerous single events, no long-term trend was observed over the time period 1222–1800 for rBC and NH+4 . In contrast, formate, VA, and p-HBA experience multi-decadal peaks reflecting periods of enhanced biomass burning. Most of the background variations and single peak events are corroborated by other ice core records from Greenland and Siberia. We suggest that the paleofire record from the LF ice core primarily reflects biomass burning episodes from northern Eurasia, induced by decadal-scale climatic variations.