Journal cover Journal topic
Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
Atmos. Chem. Phys., 15, 5047-5068, 2015
http://www.atmos-chem-phys.net/15/5047/2015/
doi:10.5194/acp-15-5047-2015
© Author(s) 2015. This work is distributed
under the Creative Commons Attribution 3.0 License.
Research article
05 May 2015
Molecular characterization of free tropospheric aerosol collected at the Pico Mountain Observatory: a case study with a long-range transported biomass burning plume
K. Dzepina1,2,*, C. Mazzoleni2,3, P. Fialho4, S. China2,3, B. Zhang2,5, R. C. Owen2,**, D. Helmig6, J. Hueber6, S. Kumar2,3,***, J. A. Perlinger2,5, L. J. Kramer2,7, M. P. Dziobak7, M. T. Ampadu1, S. Olsen8,****, D. J. Wuebbles8, and L. R. Mazzoleni1,2,7 1Department of Chemistry, Michigan Technological University, Houghton, MI, USA
2Atmospheric Science Program, Michigan Technological University, Houghton, MI, USA
3Department of Physics, Michigan Technological University, Houghton, MI, USA
4Department of Agricultural Sciences, Azores University, Angra do Heroísmo, Portugal
5Department of Civil and Environmental Engineering, Michigan Technological University, Houghton, MI, USA
6Institute of Arctic and Alpine Research (INSTAAR), University of Colorado, Boulder, CO, USA
7Department of Geological and Mining Engineering and Sciences, Michigan Technological University, Houghton, MI, USA
8Department of Atmospheric Science, University of Illinois, Urbana Champaign, IL, USA
*now at: Department of Biotechnology, University of Rijeka, Rijeka, Croatia
**now at: US EPA, Research Triangle Park, NC, USA
***now at: National Center for Medium Range Weather Forecasting, Noida, India
****now at: Xyratex International Ltd, Sacramento, CA, USA
Abstract. Free tropospheric aerosol was sampled at the Pico Mountain Observatory located at 2225 m above mean sea level on Pico Island of the Azores archipelago in the North Atlantic. The observatory is located ~ 3900 km east and downwind of North America, which enables studies of free tropospheric air transported over long distances. Aerosol samples collected on filters from June to October 2012 were analyzed to characterize organic carbon, elemental carbon, and inorganic ions. The average ambient concentration of aerosol was 0.9 ± 0.7 μg m−3. On average, organic aerosol components represent the largest mass fraction of the total measured aerosol (60 ± 51%), followed by sulfate (23 ± 28%), nitrate (13 ± 10%), chloride (2 ± 3%), and elemental carbon (2 ± 2%). Water-soluble organic matter (WSOM) extracted from two aerosol samples (9/24 and 9/25) collected consecutively during a pollution event were analyzed using ultrahigh-resolution electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry. Approximately 4000 molecular formulas were assigned to each of the mass spectra in the range of m/z 100–1000. The majority of the assigned molecular formulas had unsaturated structures with CHO and CHNO elemental compositions. FLEXPART retroplume analyses showed the sampled air masses were very aged (average plume age > 12 days). These aged aerosol WSOM compounds had an average O/C ratio of ~ 0.45, which is relatively low compared to O/C ratios of other aged aerosol. The increase in aerosol loading during the measurement period of 9/24 was linked to biomass burning emissions from North America by FLEXPART retroplume analysis and Moderate Resolution Imaging Spectroradiometer (MODIS) fire counts. This was confirmed with biomass burning markers detected in the WSOM and with the morphology and mixing state of particles as determined by scanning electron microscopy. The presence of markers characteristic of aqueous-phase reactions of phenolic species suggests that the aerosol collected at the Pico Mountain Observatory had undergone cloud processing before reaching the site. Finally, the air masses of 9/25 were more aged and influenced by marine emissions, as indicated by the presence of organosulfates and other species characteristic of marine aerosol. The change in the air masses for the two samples was corroborated by the changes in ethane, propane, and ozone, morphology of particles, as well as by the FLEXPART retroplume simulations. This paper presents the first detailed molecular characterization of free tropospheric aged aerosol intercepted at a lower free troposphere remote location and provides evidence of low oxygenation after long-range transport. We hypothesize this is a result of the selective removal of highly aged and polar species during long-range transport, because the aerosol underwent a combination of atmospheric processes during transport facilitating aqueous-phase removal (e.g., clouds processing) and fragmentation (e.g., photolysis) of components.

Citation: Dzepina, K., Mazzoleni, C., Fialho, P., China, S., Zhang, B., Owen, R. C., Helmig, D., Hueber, J., Kumar, S., Perlinger, J. A., Kramer, L. J., Dziobak, M. P., Ampadu, M. T., Olsen, S., Wuebbles, D. J., and Mazzoleni, L. R.: Molecular characterization of free tropospheric aerosol collected at the Pico Mountain Observatory: a case study with a long-range transported biomass burning plume, Atmos. Chem. Phys., 15, 5047-5068, doi:10.5194/acp-15-5047-2015, 2015.
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Short summary
Aerosol was sampled at the Pico Mountain Observatory located at 2.2km amsl on Pico Island of the North Atlantic Azores archipelago. Two aerosol samples characterized by ultrahigh resolution mass spectrometry had biomass burning and marine emissions origins, as corroborated by collocated gas- and particle-phase measurements, air masses analyses and satellites. The paper presents the first molecular characterization of aged and processed aerosol intercepted at a remote lower free troposphere
Aerosol was sampled at the Pico Mountain Observatory located at 2.2km amsl on Pico Island of the...
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