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Articles 1 - 4 of 4
Full-Text Articles in Physical Sciences and Mathematics
Sources, Distribution, And Acidity Of Sulfate-Ammonium Aerosol In The Arctic In Winter-Spring, Jenny A. Fisher, Daniel J. Jacob, Q Wang, Roya Bahreini, C C. Carouge, M J. Cubison, Jack E. Dibb, Thomas Diehl, J L. Jimenez, E M. Leibensperger, Zifeng Lu, Marcel B.J Meinders, H. O T. Pye, Patricia K. Quinn, Sangeeta Sharma, David G. Streets, Aaron Van Donkelaar, R M. Yantosca
Sources, Distribution, And Acidity Of Sulfate-Ammonium Aerosol In The Arctic In Winter-Spring, Jenny A. Fisher, Daniel J. Jacob, Q Wang, Roya Bahreini, C C. Carouge, M J. Cubison, Jack E. Dibb, Thomas Diehl, J L. Jimenez, E M. Leibensperger, Zifeng Lu, Marcel B.J Meinders, H. O T. Pye, Patricia K. Quinn, Sangeeta Sharma, David G. Streets, Aaron Van Donkelaar, R M. Yantosca
Faculty of Science - Papers (Archive)
We use GEOS-Chem chemical transport model simulations of sulfate–ammonium aerosol data from the NASA ARCTAS and NOAA ARCPAC aircraft campaigns in the North American Arctic in April 2008, together with longer-term data from surface sites, to better understand aerosol sources in the Arctic in winter–spring and the implications for aerosol acidity. Arctic pollution is dominated by transport from mid-latitudes, and we test the relevant ammonia and sulfur dioxide emission inventories in the model by comparison with wet deposition flux data over the source continents. We find that a complicated mix of natural and anthropogenic sources with different vertical signatures is …
Effects Of Aging On Organic Aerosol From Open Biomass Burning Smoke In Aircraft And Laboratory Studies, M J. Cubison, A M. Ortega, P L. Hayes, D K. Farmer, D Day, M J. Lechner, W H. Brune, E Apel, G S. Diskin, J A. Fisher, H E. Fuelberg, A Hecobian, D J. Knapp, T Mikoviny, D Riemer, G W. Sachse, W Sessions, R Weber, A J. Weinheimer, A Wisthaler, J L. Jimenez
Effects Of Aging On Organic Aerosol From Open Biomass Burning Smoke In Aircraft And Laboratory Studies, M J. Cubison, A M. Ortega, P L. Hayes, D K. Farmer, D Day, M J. Lechner, W H. Brune, E Apel, G S. Diskin, J A. Fisher, H E. Fuelberg, A Hecobian, D J. Knapp, T Mikoviny, D Riemer, G W. Sachse, W Sessions, R Weber, A J. Weinheimer, A Wisthaler, J L. Jimenez
Faculty of Science - Papers (Archive)
Biomass burning (BB) is a large source of primary and secondary organic aerosols (POA and SOA). This study addresses the physical and chemical evolution of BB organic aerosols. Firstly, the evolution and lifetime of BB POA and SOA signatures observed with the Aerodyne Aerosol Mass Spectrometer are investigated, focusing on measurements at high-latitudes acquired during the 2008 NASA ARCTAS mission, in comparison to data from other field studies and from laboratory aging experiments. The parameter f60 , the ratio of the integrated signal at m/z 60 to the total signal in the organic component mass spectrum, is used as a …
Estimated Total Emissions Of Trace Gases From The Canberra Wildfires Of 2003: A New Method Using Satellite Measurements Of Aerosol Optical Depth & The Mozart Chemical Transport Model, Clare Paton-Walsh, L Emmons, Stephen R. Wilson
Estimated Total Emissions Of Trace Gases From The Canberra Wildfires Of 2003: A New Method Using Satellite Measurements Of Aerosol Optical Depth & The Mozart Chemical Transport Model, Clare Paton-Walsh, L Emmons, Stephen R. Wilson
Faculty of Science - Papers (Archive)
In this paper we describe a new method for estimating trace gas emissions from large vegetation fires using satellite measurements of aerosol optical depth (AOD) at 550 nm, combined with an atmospheric chemical transport model. The method uses a threshold value to screen out normal levels of AOD that may be caused by raised dust, sea salt aerosols or diffuse smoke transported from distant fires. Using this method we infer an estimated total emission of 15±5 Tg of carbon monoxide, 0.05±0.02 Tg of hydrogen cyanide, 0.11±0.03 Tg of ammonia, 0.25±0.07 Tg of formaldehyde, 0.03±0.01 of acetylene, 0.10±0.03 Tg of ethylene, …
Aerosol Optical Depth At Cape Grim, Tasmania 1986-1999, Stephen R. Wilson, B. W. Forgan
Aerosol Optical Depth At Cape Grim, Tasmania 1986-1999, Stephen R. Wilson, B. W. Forgan
Faculty of Science - Papers (Archive)
The aerosol optical depth at 4 wavelengths (368, 500, 778 and 868nm) has been measured automatically at Cape Grim since 1986. The site, on the northwest tip of Tasmania, Australia was chosen to be representative of much of the southern ocean. Fourteen years of measurement have been calibrated and analyzed. The data have been filtered so that only measurements made under on-shore wind conditions are considered. The major feature observed in the record is the eruption of Mt Pinatubo, which resulted in the aerosol optical depth at 500 nm rising to 0.2 – 0.3. If the period of high stratospheric …