Insights on nitrate sources at Dome C (East Antarctic Plateau) from multi-year aerosol and snow records

© 2014 R. Traversi et al. Here we present the first multi-year record of nitrate in the atmospheric aerosol (2005-2008) and surface snow (2006-08) from central Antarctica. PM10 and size-segregated aerosol, together with superficial snow, have been collected all year-round at high resolution (daily for all the snow samples and for most of aerosol samples) at Dome C since the 2004/05 field season and analysed for main and trace ionic markers. The suitability of the sampling location in terms of possible contamination from the base is shown in detail. In spite of the relevance of nitrate in Antarctic atmosphere, both for better understanding the chemistry of N cycle in the plateau boundary layer and for improving the interpretation of long-term nitrate records from deep ice core records, nitrate sources in Antarctica are not well constrained yet, neither in extent nor in timing. A recurring seasonal pattern was pointed out in both aerosol and snow records, showing summer maxima and winter minima, although aerosol maxima lead the snow ones of 1-2 months, possibly due to a higher acidity in the atmosphere in mid-summer, favouring the repartition of nitrate as nitric acid and thus its uptake by the surface snow layers. On the basis of a meteorological analysis of one major nitrate event, of data related to PSC I extent and of irradiance values, we propose that the high nitrate summer levels in aerosol and snow are likely due to a synergy of enhanced source of nitrate and/or its precursors (such as the stratospheric inputs), higher solar irradiance and higher oxidation rates in this season. Moreover, we show here a further evidence of the substantial contribution of HNO3/NOx re-emission from the snowpack, already shown in previous works, and which can explain a significant fraction of atmospheric nitrate, maintaining the same seasonal pattern in the snow. As concerning snow specifically, the presented data suggest that nitrate is likely to be controlled mainly by atmospheric processes, not on the daily timescale but rather on the seasonal one.This research was performed in the framework of the Air-Glacs1181 'Station Concordia' project, which was funded by the MIUR through the Italian 'Programma Nazionale di Ricerche in Antartide' (PNRA) and in the framework of 'PRIDE' (2009/A2.21) and 'DECA-POL' (2010/A3.05) PNRA projects. The field operations benefited from the support of the French-Italian Concordia Station. This paper is a contribution to the HOLOCLIP project, which is funded by the European Science Foundation. This is HOLOCLIP publication no. 25. Meteorological data and information were obtained from IPEV/PNRA Project >Routine Meteorological Observation at Station Concordia - www.climantartide.it. Moreover, the authors appreciate the support of the AMRC, SSEC, UW-Madison for the data set, NSF grant numbers ANT-0944018 and ANT-1245663. B. Funke was supported by the Spanish MCINN under grant AYA2011-23552 and EC FEDER funds. We are grateful to the anonymous reviewers whose comments markedly improved the final manuscript.Peer Reviewe

Insights on nitrate sources at Dome C (East Antarctic Plateau) from multi-year aerosol and snow records

Here we present the first multi-year record of nitrate in the atmospheric aerosol (2005–2008) and surface snow (2006–08) from central Antarctica. PM10 and size-segregated aerosol, together with superficial snow, have been collected all year-round at high resolution (daily for all the snow samples and for most of aerosol samples) at Dome C since the 2004/05 field season and analysed for main and trace ionic markers. The suitability of the sampling location in terms of possible contamination from the base is shown in detail. In spite of the relevance of nitrate in Antarctic atmosphere, both for better understanding the chemistry of N cycle in the plateau boundary layer and for improving the interpretation of long-term nitrate records from deep ice core records, nitrate sources in Antarctica are not well constrained yet, neither in extent nor in timing. A recurring seasonal pattern was pointed out in both aerosol and snow records, showing summer maxima and winter minima, although aerosol maxima lead the snow ones of 1–2 months, possibly due to a higher acidity in the atmosphere in mid-summer, favouring the repartition of nitrate as nitric acid and thus its uptake by the surface snow layers. On the basis of a meteorological analysis of one major nitrate event, of data related to PSC I extent and of irradiance values, we propose that the high nitrate summer levels in aerosol and snow are likely due to a synergy of enhanced source of nitrate and/or its precursors (such as the stratospheric inputs), higher solar irradiance and higher oxidation rates in this season. Moreover, we show here a further evidence of the substantial contribution of HNO3/NOx re-emission from the snowpack, already shown in previous works, and which can explain a significant fraction of atmospheric nitrate, maintaining the same seasonal pattern in the snow. As concerning snow specifically, the presented data suggest that nitrate is likely to be controlled mainly by atmospheric processes, not on the daily timescale but rather on the seasonal one