Aerosol measurements at a high-elevation site: composition, size, and cloud condensation nuclei activity

被引:17
作者
Friedman, B. [1 ]
Zelenyuk, A. [2 ]
Beranek, J. [2 ]
Kulkarni, G. [2 ]
Pekour, M. [2 ]
Hallar, A. Gannet [3 ]
McCubbin, I. B. [3 ]
Thornton, J. A. [1 ]
Cziczo, D. J. [4 ]
机构
[1] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
[2] Pacific NW Natl Lab, Richland, WA 99352 USA
[3] Desert Res Inst, Storm Peak Lab, Steamboat Springs, CO USA
[4] MIT, Dept Earth Atmospher & Planetary Sci, Cambridge, MA USA
关键词
PARTICLE FORMATION; HYGROSCOPIC PROPERTIES; NUMBER CONCENTRATION; CCN CONCENTRATIONS; SOLUBLE ORGANICS; MIXING STATE; ACTIVATION; CAPABILITIES; CHEMISTRY; PARAMETER;
D O I
10.5194/acp-13-11839-2013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Measurements of cloud condensation nuclei (CCN) concentrations, single particle composition and size distributions at a high-elevation research site from March 2011 are presented. The temporal evolution of detailed single particle composition is compared with changes in CCN activation on four days, two of which include new particle formation and growth events. Sulfate-containing particles dominated the single particle composition by number; biomass burning particles, sea salt particles, and particles containing organic components were also present. CCN activation largely followed the behavior of the sulfate-containing particle types; biomass burning particle types also likely contained hygroscopic material that impacted CCN activation. Newly formed particles also may contribute to CCN activation at higher supersaturation conditions. Derived aerosol hygroscopicity parameters from the size distribution and CCN concentration measurements are within the range of previous reports of remote continental kappa values.
引用
收藏
页码:11839 / 11851
页数:13
相关论文
共 64 条
  • [1] Cloud condensation nucleus activity of internally mixed ammonium sulfate/organic acid aerosol particles
    Abbatt, JPD
    Broekhuizen, K
    Kumal, PP
    [J]. ATMOSPHERIC ENVIRONMENT, 2005, 39 (26) : 4767 - 4778
  • [2] AEROSOLS, CLOUD MICROPHYSICS, AND FRACTIONAL CLOUDINESS
    ALBRECHT, BA
    [J]. SCIENCE, 1989, 245 (4923) : 1227 - 1230
  • [3] Aerosol-cloud-precipitation interactions. Part 1. The nature and sources of cloud-active aerosols
    Andreae, M. O.
    Rosenfeld, D.
    [J]. EARTH-SCIENCE REVIEWS, 2008, 89 (1-2) : 13 - 41
  • [4] Airborne cloud condensation nuclei measurements during the 2006 Texas Air Quality Study
    Asa-Awuku, Akua
    Moore, Richard H.
    Nenes, Athanasios
    Bahreini, Roya
    Holloway, John S.
    Brock, Charles A.
    Middlebrook, Ann M.
    Ryerson, Thomas B.
    Jimenez, Jose L.
    DeCarlo, Peter F.
    Hecobian, Arsineh
    Weber, Rodney J.
    Stickel, Robert
    Tanner, Dave J.
    Huey, Lewis G.
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2011, 116
  • [5] Importance of aerosol composition, mixing state, and morphology for heterogeneous ice nucleation: A combined field and laboratory approach
    Baustian, Kelly J.
    Cziczo, Daniel J.
    Wise, Matthew E.
    Pratt, Kerri A.
    Kulkarni, Gourihar
    Hallar, A. Gannet
    Tolbert, Margaret A.
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2012, 117
  • [6] CCN activation of slightly soluble organics: the importance of small amounts of inorganic salt and particle phase
    Bilde, M
    Svenningsson, B
    [J]. TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY, 2004, 56 (02): : 128 - 134
  • [7] Borys RD, 1997, B AM METEOROL SOC, V78, P2115, DOI 10.1175/1520-0477(1997)078<2115:SPLART>2.0.CO
  • [8] 2
  • [9] Partially soluble organics as cloud condensation nuclei: Role of trace soluble and surface active species
    Broekhuizen, K
    Kumar, PP
    Abbatt, JPD
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2004, 31 (01) : L011071 - 5
  • [10] Comparison between measured and predicted CCN concentrations at Egbert, Ontario: Focus on the organic aerosol fraction at a semi-rural site
    Chang, R. Y. -W.
    Liu, P. S. K.
    Leaitch, W. R.
    Abbatt, J. P. D.
    [J]. ATMOSPHERIC ENVIRONMENT, 2007, 41 (37) : 8172 - 8182