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In Situ Chemical Characterization of Aged Biomass-Burning Aerosols Impacting Cold Wave Clouds

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dc.creator Pratt, Kerri A.
dc.creator Heymsfield, Andrew J.
dc.creator Twohy, Cynthia
dc.creator Murphy, Shane M.
dc.creator DeMott, Paul J.
dc.creator Hudson, James G.
dc.creator Subramanian, R.
dc.creator Wang, Zhien
dc.creator Seinfeld, John H.
dc.creator Prather, Kimberly A.
dc.date.accessioned 2011-12-30T17:22:02Z
dc.date.available 2011-12-30T17:22:02Z
dc.date.issued 2010-08
dc.identifier.citation Pratt, Kerri A., and Coauthors, 2010: In Situ Chemical Characterization of Aged Biomass-Burning Aerosols Impacting Cold Wave Clouds. Journal of the Atmospheric Sciences, 67(8), 2451–2468. en_US
dc.identifier.uri http://hdl.handle.net/1957/26418
dc.description.abstract During the Ice in Clouds Experiment–Layer Clouds (ICE-L), aged biomass-burning particles were identified within two orographic wave cloud regions over Wyoming using single-particle mass spectrometry and electron microscopy. Using a suite of instrumentation, particle chemistry was characterized in tandem with cloud microphysics. The aged biomass-burning particles comprised ~30%–40% by number of the 0.1–1.0-μm clear-air particles and were composed of potassium, organic carbon, elemental carbon, and sulfate. Aerosol mass spectrometry measurements suggested these cloud-processed particles were predominantly sulfate by mass. The first cloud region sampled was characterized by primarily homogeneously nucleated ice particles formed at temperatures near −40°C. The second cloud period was characterized by high cloud droplet concentrations (~150–300 cm⁻³) and lower heterogeneously nucleated ice concentrations (7–18 L⁻¹) at cloud temperatures of −24° to −25°C. As expected for the observed particle chemistry and dynamics of the observed wave clouds, few significant differences were observed between the clear-air particles and cloud residues. However, suggestive of a possible heterogeneous nucleation mechanism within the first cloud region, ice residues showed enrichments in the number fractions of soot and mass fractions of black carbon, measured by a single-particle mass spectrometer and a single-particle soot photometer, respectively. In addition, enrichment of biomass-burning particles internally mixed with oxalic acid in both the homogeneously nucleated ice and cloud droplets compared to clear air suggests either preferential activation as cloud condensation nuclei or aqueous phase cloud processing. en_US
dc.description.sponsorship NSF andNCARare acknowledged for financial support of the ICE-L field campaign, as well as the work of A. J. Heymsfield. K. A. Pratt and K. A. Prather acknowledge NSF for support of ICE-L (ATM- 0650659), A-ATOFMS development (ATM-0321362), and a graduate research fellowship for K. A. Pratt. S. M. Murphy and J. H. Seinfeld acknowledge NSF for support of ICE-L (ATM-0340832) and NASA for an Earth and Space Sciences Fellowship for S. M. Murphy. C. H. Twohy, P. J. DeMott, J. G. Hudson, R. Subramanian, and Z. Wang acknowledge NSF for ICE-L support (ATM-0612605, ATM-0611936, ATM-0615414, ATM- 0631919, andATM-0645644, respectively). en_US
dc.language.iso en_US en_US
dc.publisher American Meteorological Society en_US
dc.relation.ispartofseries Journal of the Atmospheric Sciences en_US
dc.relation.ispartofseries Vol. 67 no. 8 en_US
dc.title In Situ Chemical Characterization of Aged Biomass-Burning Aerosols Impacting Cold Wave Clouds en_US
dc.type Article en_US
dc.description.peerreview yes en_US
dc.identifier.doi 10.1175/2010JAS3330.1


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