Ammonia in the summertime Arctic marine boundary layer: sources, sinks, and implications

oleh: G. R. Wentworth, J. G. Murphy, B. Croft, R. V. Martin, J. R. Pierce, J. R. Pierce, J.-S. Côté, I. Courchesne, J.-É. Tremblay, J. Gagnon, J. L. Thomas, S. Sharma, D. Toom-Sauntry, A. Chivulescu, M. Levasseur, J. P. D. Abbatt

Format: Article
Diterbitkan: Copernicus Publications 2016-02-01

Deskripsi

Continuous hourly measurements of gas-phase ammonia (NH<sub>3(g)</sub>) were taken from 13 July to 7 August 2014 on a research cruise throughout Baffin Bay and the eastern Canadian Arctic Archipelago. Concentrations ranged from 30 to 650 ng m<sup>−3</sup> (40–870 pptv) with the highest values recorded in Lancaster Sound (74°13′ N, 84°00′ W). Simultaneous measurements of total ammonium ([NH<sub><i>x</i></sub>]), pH and temperature in the ocean and in melt ponds were used to compute the compensation point (<i>χ</i>), which is the ambient NH<sub>3(g)</sub> concentration at which surface–air fluxes change direction. Ambient NH<sub>3(g)</sub> was usually several orders of magnitude larger than both <i>χ</i><sub>ocean</sub> and <i>χ</i><sub>MP</sub> (&lt; 0.4–10 ng m<sup>3</sup>) indicating these surface pools are net sinks of NH<sub>3</sub>. Flux calculations estimate average net downward fluxes of 1.4 and 1.1 ng m<sup>−2</sup> s<sup>−1</sup> for the open ocean and melt ponds, respectively. Sufficient NH<sub>3(g)</sub> was present to neutralize non-sea-salt sulfate (nss-SO<sub>4</sub><sup>2−</sup>) in the boundary layer during most of the study. This finding was corroborated with a historical data set of PM<sub>2.5</sub> composition from Alert, Nunavut (82°30′ N, 62°20′ W) wherein the median ratio of NH<sub>4</sub><sup>+</sup>/nss-SO<sub>4</sub><sup>2−</sup> equivalents was greater than 0.75 in June, July and August. The GEOS-Chem chemical transport model was employed to examine the impact of NH<sub>3(g)</sub> emissions from seabird guano on boundary-layer composition and nss-SO<sub>4</sub><sup>2−</sup> neutralization. A GEOS-Chem simulation without seabird emissions underestimated boundary layer NH<sub>3(g)</sub> by several orders of magnitude and yielded highly acidic aerosol. A simulation that included seabird NH<sub>3</sub> emissions was in better agreement with observations for both NH<sub>3(g)</sub> concentrations and nss-SO<sub>4</sub><sup>2−</sup> neutralization. This is strong evidence that seabird colonies are significant sources of NH<sub>3</sub> in the summertime Arctic, and are ubiquitous enough to impact atmospheric composition across the entire Baffin Bay region. Large wildfires in the Northwest Territories were likely an important source of NH<sub>3</sub>, but their influence was probably limited to the Central Canadian Arctic. Implications of seabird-derived N-deposition to terrestrial and aquatic ecosystems are also discussed.