Atmospheric Chemistry and Physics (Oct 2018)
Multi-year chemical composition of the fine-aerosol fraction in Athens, Greece, with emphasis on the contribution of residential heating in wintertime
Abstract
In an attempt to take effective action towards mitigating pollution episodes in Athens, precise knowledge of PM2.5 composition and its sources is a prerequisite. Thus, a 2-year chemical composition dataset from aerosol samples collected in an urban background site in central Athens from December 2013 to March 2016 has been obtained and a positive matrix factorization (PMF) was applied in order to identify and apportion fine aerosols to their sources. A total of 850 aerosol samples were collected on a 12 to 24 h basis and analyzed for major ions, trace elements, and organic and elemental carbon, allowing us to further assess the impact of residential heating as a source of air pollution over Athens.The ionic and carbonaceous components were found to constitute the major fraction of the PM2.5 aerosol mass. The annual contribution of the ion mass (IM), particulate organic mass (POM), dust, elemental carbon (EC), and sea salt (SS) was calculated at 31 %, 38 %, 18 %, 8 %, and 3 %, respectively, and exhibited considerable seasonal variation. In winter, the share of IM was estimated down to 23 %, with POM + EC being the dominant component accounting for 52 % of the PM2.5 mass, while in summer, IM (42 %) and carbonaceous aerosols (41 %) contributed almost equally.Results from samples collected on a 12 h basis (day and night) during the three intensive winter campaigns indicated the impact of heating on the levels of a series of compounds. Indeed, PM2.5, EC, POM, NO3−, C2O42−, non sea salt (nss) K+ and selected trace metals including Cd and Pb were increased by up to a factor of 4 in the night compared to the day, highlighting the importance of heating on air quality in Athens. Furthermore, in order to better characterize wintertime aerosol sources and quantify the impact of biomass burning on PM2.5 levels, source apportionment was performed. The data can be interpreted on the basis of six sources, namely biomass burning (31 %), vehicular emissions (19 %), heavy oil combustion (7 %), regional secondary (21 %), marine aerosols (9 %), and dust particles (8 %). Regarding night-to-day patterns their contributions shifted from 19 %, 19 %, 8 %, 31 %, 12 %, and 10 % of the PM2.5 mass during day to 39 %, 19 %, 6 %, 14 %, 7 %, and 7 % during the night, underlining the significance of biomass burning as the main contributor to fine particle levels during nighttime in winter.