Dominance of organic aerosols in the marine boundary layer over the Gulf of Maine during NEAQS 2002 and their role in aerosol light scattering

被引:51
作者
Bates, TS
Quinn, PK
Coffman, DJ
Johnson, JE
Middlebrook, AM
机构
[1] NOAA, Pacific Marine Environm Lab, Seattle, WA 98115 USA
[2] NOAA, Aeron Lab, Boulder, CO 80303 USA
[3] Univ Washington, Joint Inst Study Atmosphere & Oceans, Seattle, WA 98195 USA
关键词
D O I
10.1029/2005JD005797
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Aerosol chemical, physical, and optical measurements were made aboard the NOAA R/V Ronald H. Brown off the coast of New England from July 12 through August 10, 2002, as part of the New England Air Quality Study (NEAQS). Measurements (generally 20 to 100 km from the coast) were made downwind of urban centers (New York City, Boston) and rural areas, and in air masses that had not been in contact with land for several days. On average during NEAQS, 75 +/- 8% of the sub-10 mu m aerodynamic diameter dry aerosol mass sampled 18 m above the sea surface was in the sub-10 mu m fraction ( size cut at 55% RH). The major submicrometer aerosol components were ammonium sulfate and particulate organic matter (POM, defined here as 1.6 times the mass concentration of organic carbon) comprising more than 92 +/- 4% of the total mass. Under northwesterly flow with an average submicrometer total mass concentrations of 11 +/- 4.5 mg m(-3), POM was the dominant component (68 +/- 8%) followed by (NH4)(x)HySO4 (23 +/- 8%), inorganic oxidized material (IOM) (6 +/- 4%), and EC ( 3 +/- 1%). Under southwesterly flow with an average submicrometer total mass concentrations of 30 +/- 11 mu g m (-3), (NH4)(x)HySO4 was the dominant component (54 +/- 9%) followed by POM (41 +/- 9%), IOM (3 +/- 2%), and EC ( 2 +/- 1%). Mie calculations using submicrometer nonrefractory (R) POM and NR (NH4)(x)HySO4 + H2O size distributions to calculate submicrometer light scattering (sigma(sp)) at a wavelength of 550 nm suggest that POM was a dominant chemical component contributing to aerosol light scattering ( haze) during NEAQS 2002, and contributed 60 +/- 6 % and 57 +/- 11 % to sigma(sp) at 55% RH during two pollution episodes off the New England Coast. These results are similar to those from the mid-Atlantic states during TARFOX but contrary to the long-term monitoring measurements over the continental northeast United States that show the New England haze is primarily a result of sulfate aerosol.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 47 条
  • [1] Quantitative sampling using an Aerodyne aerosol mass spectrometer - 1. Techniques of data interpretation and error analysis
    Allan, JD
    Jimenez, JL
    Williams, PI
    Alfarra, MR
    Bower, KN
    Jayne, JT
    Coe, H
    Worsnop, DR
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2003, 108 (D3)
  • [2] Determining aerosol radiative properties using the TSI 3563 integrating nephelometer
    Anderson, TL
    Ogren, JA
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 1998, 29 (01) : 57 - 69
  • [3] SOOT CARBON AND EXCESS FINE POTASSIUM - LONG-RANGE TRANSPORT OF COMBUSTION-DERIVED AEROSOLS
    ANDREAE, MO
    [J]. SCIENCE, 1983, 220 (4602) : 1148 - 1151
  • [4] Coastal boundary layer influence on pollutant transport in New England
    Angevine, WM
    Senff, CJ
    White, AB
    Williams, EJ
    Koermer, J
    Miller, STK
    Talbot, R
    Johnston, PE
    McKeen, SA
    Downs, T
    [J]. JOURNAL OF APPLIED METEOROLOGY, 2004, 43 (10): : 1425 - 1437
  • [5] [Anonymous], PARTICULATE MONITORI
  • [6] [Anonymous], 2001, Climate Change 2001:Impacts, Adaptation and Vulnerability
  • [7] Regional marine boundary layer aerosol size distributions in the Indian, Atlantic, and Pacific Oceans: A comparison of INDOEX measurements with ACE-1, ACE-2, and Aerosols99
    Bates, TS
    Coffman, DJ
    Covert, DS
    Quinn, PK
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D19)
  • [8] SIZE DISTRIBUTION OF THE URBAN AEROSOL IN VIENNA
    BERNER, A
    LURZER, C
    POHL, F
    PREINING, O
    WAGNER, P
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 1979, 13 (03) : 245 - 261
  • [9] General circulation model assessment of the sensitivity of direct climate forcing by anthropogenic sulfate aerosols to aerosol size and chemistry
    Boucher, O
    Anderson, TL
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1995, 100 (D12) : 26117 - 26134
  • [10] Nighttime removal of NOx in the summer marine boundary layer -: art. no. L07108
    Brown, SS
    Dibb, JE
    Stark, H
    Aldener, M
    Vozella, M
    Whitlow, S
    Williams, EJ
    Lerner, BM
    Jakoubek, R
    Middlebrook, AM
    DeGouw, JA
    Warneke, C
    Goldan, PD
    Kuster, WC
    Angevine, WM
    Sueper, DT
    Quinn, PK
    Bates, TS
    Meagher, JF
    Fehsenfeld, FC
    Ravishankara, AR
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2004, 31 (07) : L071081 - 5