Chemical characterization of aerosols on the east coast of the United States using aircraft and ground-based stations during the CLAMS experiment

被引:15
作者
Castanho, ADD
Martins, JV
Hobbs, PV
Artaxo, P
Remer, L
Yamasoe, M
Colarco, PR
机构
[1] Univ Sao Paulo, Inst Phys, BR-05508900 Sao Paulo, Brazil
[2] Univ Maryland, JCET, Baltimore, MD 21201 USA
[3] NASA, Goddard Space Flight Ctr, Greenbelt, MD 20771 USA
[4] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
[5] Univ Sao Paulo, Inst Astron Geophys & Atmospher Sci, BR-05508900 Sao Paulo, Brazil
[6] Univ Maryland Baltimore Cty, Earth Syst Sci Interdisciplinary Ctr, Baltimore, MD 21201 USA
关键词
D O I
10.1175/JAS3388.1
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The Chesapeake Lighthouse and Aircraft Measurements for Satellites (CLAMS) experiment was carried out off the central East Coast of the United States in July 2001. During CLAMS, aerosol particle mass was measured at two ground stations and on the University of Washington's Convair 580 research aircraft. Physical and chemical characteristics of the aerosols were identified and quantified. Three main aerosol regimes were identified in the region and are discussed in this work: local pollution/sea salt back,ground, long-range transported dust, and long-range transported pollution. The major component measured in the fine mode of the aerosol on the ground at Wallops Island, Virginia, was sulfate, estimated as NH4HSO4, which accounted for 55% +/- 9% on average of the fine particle mass (FPM) during the experiment period. Black carbon concentrations accounted for 3% +/- 1% of FPM; soil dust was also present, representing on average 6% +/- 8% of FPM. The difference between the sum of the masses of the measured compounds and the total fine particle mass was 36% +/- 10% of FPM, which is attributed primarily to nitrates and organic carbon that were not measured. Aerosol chemical composition in the atmospheric column is also discussed and compared with ground-based measurements. Aerosol dust concentration reached 40% of FPM during an incursion of Saharan dust between 24 and 26 July. Sulfate aerosol reached 70% of FPM during the transport of regional pollution on 17 July. Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol optical thickness, coupled with air parcel back trajectories, supported the conclusion of episodes of long-range transport of dust from the Sahara Desert and pollutants from the continental United States.
引用
收藏
页码:934 / 946
页数:13
相关论文
共 25 条
  • [1] [Anonymous], PARTICLE INDUCED XRA
  • [2] PIXE AND RECEPTOR MODELS APPLIED TO REMOTE AEROSOL SOURCE APPORTIONMENT IN BRAZIL
    ARTAXO, P
    ORSINI, C
    [J]. NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 1987, 22 (1-3) : 259 - 263
  • [3] Wintertime and summertime Sao Paulo aerosol source apportionment study
    Cantanho, ADA
    Artaxo, P
    [J]. ATMOSPHERIC ENVIRONMENT, 2001, 35 (29) : 4889 - 4902
  • [4] Saharan dust transport to the Caribbean during PRIDE: 2. Transport, vertical profiles, and deposition in simulations of in situ and remote sensing observations
    Colarco, PR
    Toon, OB
    Reid, JS
    Livingston, JM
    Russell, PB
    Redemann, J
    Schmid, B
    Maring, HB
    Savoie, D
    Welton, EJ
    Campbell, JR
    Holben, BN
    Levy, R
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2003, 108 (D19)
  • [5] Chemical apportionment of aerosol column optical depth off the mid-Atlantic coast of the United States
    Hegg, DA
    Livingston, J
    Hobbs, PV
    Novakov, T
    Russell, P
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D21) : 25293 - 25303
  • [6] AERONET - A federated instrument network and data archive for aerosol characterization
    Holben, BN
    Eck, TF
    Slutsker, I
    Tanre, D
    Buis, JP
    Setzer, A
    Vermote, E
    Reagan, JA
    Kaufman, YJ
    Nakajima, T
    Lavenu, F
    Jankowiak, I
    Smirnov, A
    [J]. REMOTE SENSING OF ENVIRONMENT, 1998, 66 (01) : 1 - 16
  • [7] Hopke P. K., 1991, RECEPTOR MODELING AI
  • [8] Characterization of the gent stacked filter unit PM10 sampler
    Hopke, PK
    Xie, Y
    Raunemaa, T
    Biegalski, S
    Landsberger, S
    Maenhaut, W
    Artaxo, P
    Cohen, D
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 1997, 27 (06) : 726 - 735
  • [9] KALNAY E, 1990, B AM METEOROL SOC, V71, P1410, DOI 10.1175/1520-0477(1990)071<1410:GNWPAT>2.0.CO
  • [10] 2