Air quality monitoring in communities of the Canadian Arctic during the high shipping season with a focus on local and marine pollution
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Published:2015-03-09
Issue:5
Volume:15
Page:2651-2673
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ISSN:1680-7324
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Container-title:Atmospheric Chemistry and Physics
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language:en
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Short-container-title:Atmos. Chem. Phys.
Author:
Aliabadi A. A., Staebler R. M.ORCID, Sharma S.
Abstract
Abstract. The Canadian Arctic has experienced decreasing sea ice extent and increasing shipping activity in recent decades. While there are economic incentives to develop resources in the north, there are environmental concerns that increasing marine traffic will contribute to declining air quality in northern communities. In an effort to characterize the relative impact of shipping on air quality in the north, two monitoring stations have been installed in Cape Dorset and Resolute, Nunavut, and have been operational since 1 June 2013. The impact of shipping and other sources of emissions on NOx, O3, SO2, BC, and PM2.5 pollution have been characterized for the 2013 shipping season from 1 June to 1 November. In addition, a high-resolution Air Quality Health Index (AQHI) for both sites was computed. Shipping consistently increased O3 mixing ratio and PM2.5 concentration. The 90% confidence interval for mean difference in O3 mixing ratio between ship- and no ship-influenced air masses were up to 4.6–4.7 ppb and 2.5–2.7 ppb for Cape Dorset and Resolute, respectively. The same intervals for PM2.5 concentrations were up to 1.8–1.9 μg m−3 and 0.5–0.6 μg m−3. Ship-influenced air masses consistently exhibited an increase of 0.1 to 0.3 in the high-resolution AQHI compared to no ship-influenced air masses. Trajectory cluster analysis in combination with ship traffic tracking provided an estimated range for percent ship contribution to NOx, O3, SO2, and PM2.5 that were 12.9–17.5 %, 16.2–18.1 %, 16.9–18.3 %, and 19.5–31.7 % for Cape Dorset and 1.0–7.2 %, 2.9–4.8 %, 5.5–10.0 %, and 6.5–7.2 % for Resolute during the 2013 shipping season. Additional measurements in Resolute suggested that percent ship contribution to black carbon was 4.3–9.8 % and that black carbon constituted 1.3–9.7 % of total PM2.5 mass in ship plumes. Continued air quality monitoring in the above sites for future shipping seasons will improve the statistics in our analysis and characterize repeating seasonal patterns in air quality due to shipping, local pollution, and long-range transport.
Publisher
Copernicus GmbH
Subject
Atmospheric Science
Reference60 articles.
1. Bond, T. C., Anderson, T. L., and Campbell, D.: Calibration and intercomparison of filter-based measurements of visible light absorption by aerosols, Aerosol Sci. Tech., 30, 582–600, https://doi.org/10.1080/027868299304435, 1999. 2. Brigham, L., McCalla, R., Cunningham, E., Barr, W., Vanderzaag, D., Chircop, A., Santos-Pedro, V., MacDonald, R., Harder, S., Ellis, B., Snyder, J., Huntington, H., Skjoldal, H., Williams, M., Wojhan, T., and Falkingham, J.: Arctic Marine Shipping Assessment, Report, Arctic Council, Tromsø, Norway, available at: http://library.arcticportal.org/1400/ (last access: 3 March 2014), 2009. 3. Browse, J., Carslaw, K. S., Schmidt, A., and Corbett, J. J.: Impact of future Arctic shipping on high-latitude black carbon deposition, Geophys. Res. Lett., 40, 4459–4463, https://doi.org/10.1002/grl.50876, 2013. 4. Bulletin: Ship Safety Bulletin: New regulations for vessel air emissions, ship to ship transfer of oil, and greywater, Bulletin 06/2013, Transport Canada, Marine Safety and Security, Tower C, Place de Ville, 10th Floor, 330 Sparks Street, Ottawa, ON K1A 0N8, available at: http://www.tc.gc.ca/media/documents/marinesafety/SSB-06-2013E.pdf (last access: 10 July 2014), 2013. 5. Capaldo, K. P. and Pandis, S. N.: Dimethylsulfide chemistry in the remote marine atmosphere: evaluation and sensitivity analysis of available mechanisms, J. Geophys. Res.-Atmos., 102, 23251–23267, https://doi.org/10.1029/97JD01807, 1997.
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