A11C-0057
Aerosol Size and Chemical Composition in the Canadian High Arctic

Monday, 14 December 2015
Poster Hall (Moscone South)
Rachel Ying-Wen Chang1, Patrick L Hayes2, Warren Richard Leaitch3, Betty Croft1, Norman T. O'Neill4, Pierre Fogal5, James R Drummond1 and James J Sloan6, (1)Dalhousie University, Halifax, NS, Canada, (2)University of Montreal, Montreal, QC, Canada, (3)Environment Canada, Toronto, ON, Canada, (4)University of Sherbrooke, Sherbrooke, QC, Canada, (5)University of Toronto, Physics, Toronto, ON, Canada, (6)University of Waterloo, Waterloo, ON, Canada
Abstract:
Arctic aerosol have a strong annual cycle, with winter months dominated by long range transport from lower latitudes resulting in high mass loadings. Conversely, local emissions are more prominent in the summer months because of the decreased influence of transported aerosol, allowing us to regularly observe both transported and local aerosol. This study will present observations of aerosol chemical composition and particle number size distribution collected at the Polar Environment Artic Research Laboratory and the Alert Global Atmospheric Watch Observatory at Eureka (80N, 86W) and Alert (82N, 62W), Nunavut, respectively. Summer time observations of the number size distribution reveal a persistent mode of particles centered between 30-50 nm, with occasional bursts of smaller particles. The non-refractory aerosol chemical composition, measured by the Canadian Network for the Detection of Atmospheric Change quadrupole aerosol mass spectrometer, is primarily organic, with contributions from both aged and fresher organic aerosol. Factor analysis will be conducted to better understand these sources. The site at Eureka is more susceptible to long range transport since it is at the top of a mountain ridge (610 m above sea level) and will be compared to the site at Alert on an elevated plain (200 m above sea level). This will allow us to determine the relative contributions from processes and sources at the sites at different elevations. Comparisons with aerosol optical depth and GEOS-Chem model output will also be presented to put these surface measurements into context with the overlying and regional atmosphere. Results from this study contribute to our knowledge of aerosol in the high Arctic.