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Transported acid aerosols measured in southern Ontario
Institution:1. School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou 510006, PR China;2. Instrumental Analysis Center, Guangdong University of Technology, Guangzhou 510006, PR China;1. Department of City and Regional Planning, University of North Carolina, Chapel Hill, NC, USA;2. Interdisciplinary Studies Department, Howard University, Washington, DC, USA;3. School of Environmental and Forest Sciences, University of Washington, Seattle, WA, USA;4. Department of Environmental & Occupational Health Sciences, University of Washington, Seattle, WA, USA;5. Partnerships and Programs, Vulcan LLC, Seattle, WA, USA;6. Department of Environmental Health Sciences, Jonathan and Karin Fielding School of Public Health, University of California, Los Angeles, CA, USA;7. United States Environmental Protection Agency, Office of Research and Development, Durham, NC, USA;8. The Nature Conservancy, Portland, OR, USA;1. NSW Bushfire Risk Management Research Hub, Wollongong, NSW 2522, Australia;2. School of Earth, Atmospheric and Life Sciences, University of Wollongong, NSW 2522, Australia;3. Research Program, Bureau of Meteorology, Hobart, TAS 7000, Australia
Abstract:During the period 29 June 1986–9 August 1986, a field health study assessing the acute health effects of air pollutants on children was conducted at a summer girls' camp on the northern shore of Lake Erie in SW Ontario. Continuous air pollution measurements of SO2, O3, NOx, particulate sulfates, light scattering, and meteorological measurements including temperature, dew point, and wind speed and direction were made. Twelve-hour integrated samples of size fractioned particles were also obtained using dichotomous samplers and Harvard impactors equipped with an ammonia denuder for subsequent hydrogen ion determination. Particulate samples were analyzed for trace elements by X-ray fluorescence and Neutron Activation, and for organic and elemental carbon by a thermal/optical technique. The measured aerosol was periodically very acidic with observed 12-h averaged H+ concentrations in the range < 10–560 nmoles m−3. The aerosol H+ appeared to represent the net strong acidity after H2SO4 reaction with NH3(g). Average daytime concentrations were higher than night-time for aerosol H+, sulfate, fine mass and ozone. Prolonged episodes of atmospheric acidity, sulfate, and ozone were associated with air masses arriving at the measurement site from the west and from the southwest over Lake Erie. Sulfate concentrations measured at the lakeshore camp were more than twice those measured at inland sites during extreme pollution episodes. The concentration gradient observed with onshore flow was potentially due to enhanced deposition near the lakeshore caused by discontinuities in the meteorological fields in this region.
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