HR: 17:46h
AN: A24C-08    [Abstracts]
TI: Fast airborne aerosol size and composition measurements from the NCAR C-130 during the MIRAGE-Mex 2006 field campaign
AU: * DeCarlo, P F
EM: decarlop@colorado.edu
AF: CIRES, University of Colorado, 216 UCB, Boulder, CO 80309, United States
AU: * DeCarlo, P F
EM: decarlop@colorado.edu
AF: Dept of Atmospheric and Oceanic Science, Univ. of Colorado, 318 UCB, Boulder, CO 80309, United States
AU: Dunlea, E
EM: edward.dunlea@colorado.edu
AF: CIRES, University of Colorado, 216 UCB, Boulder, CO 80309, United States
AU: Kimmel, J
EM: joel.kimmel@colorado.edu
AF: CIRES, University of Colorado, 216 UCB, Boulder, CO 80309, United States
AU: Ulbrich, I
EM: Ingrid.Ulbrich@Colorado.EDU
AF: CIRES, University of Colorado, 216 UCB, Boulder, CO 80309, United States
AU: Ulbrich, I
EM: Ingrid.Ulbrich@Colorado.EDU
AF: Dept. of Chemistry, Univ. of Colorado, 215 UCB, Boulder, CO 80309, United States
AU: Aiken, A
EM: allison.aiken@colorado.edu
AF: CIRES, University of Colorado, 216 UCB, Boulder, CO 80309, United States
AU: Aiken, A
EM: allison.aiken@colorado.edu
AF: Dept. of Chemistry, Univ. of Colorado, 215 UCB, Boulder, CO 80309, United States
AU: Crounse, J
EM: crounjd@caltech.edu
AF: Geology and Planetary Science, California Inst. of Tech., MC 170-25 1200 E. California Blvd., Pasadena, CA 91125, United States
AU: Wennberg, P
EM: wennberg@gps.caltech.edu
AF: Geology and Planetary Science, California Inst. of Tech., MC 170-25 1200 E. California Blvd., Pasadena, CA 91125, United States
AU: Shinozuka, Y
EM: yohei@hawaii.edu
AF: Department of Oceanography, University of Hawaii, 1000 Pope Rd, Honolulu, HI 96822, United States
AU: Clarke, T
EM: tclarke@soest.hawaii.edu
AF: Department of Oceanography, University of Hawaii, 1000 Pope Rd, Honolulu, HI 96822, United States
AU: Zhao, J
EM: jczhou@hawaii.edu
AF: Department of Oceanography, University of Hawaii, 1000 Pope Rd, Honolulu, HI 96822, United States
AU: Tomlinson, J
EM: jason.tomlinson@tamu.edu
AF: Dept. of Atm. Sci., College of Geosciences, Texas A&M Univ., 3150 TAMU, College Station, TX 77843, United States
AU: Collins, D
EM: dcollins@tamu.edu
AF: Dept. of Atm. Sci., College of Geosciences, Texas A&M Univ., 3150 TAMU, College Station, TX 77843, United States
AU: Campos, T
EM: campos@ucar.edu
AF: NCAR, PO Box 3000, Boulder, CO 80307, United States
AU: Jimenez, J L
EM: jose.jimenez@colorado.edu
AF: CIRES, University of Colorado, 216 UCB, Boulder, CO 80309, United States
AU: Jimenez, J L
EM: jose.jimenez@colorado.edu
AF: Dept. of Chemistry, Univ. of Colorado, 215 UCB, Boulder, CO 80309, United States
AB: A high mass resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, DeCarlo et al., 2006) was deployed for the first time on an airborne platform during the MIRAGE-Mex campaign on the NCAR C-130 research aircraft, for measurements of size-resolved non-refractory sulfate, nitrate, ammonium, chloride, and organics. Onboard the C-130 the HR-ToF-AMS was operated in a medium resolution mode known as "V-ToF mode", providing added chemical resolution of the measured aerosol, while still maintaining good spatial (time) resolution and allowing the measurement of size distributions. Organic aerosol (OA) accounted for approximately half of the non-refractory submicron aerosol mass and showed strong correlation with gas phase measurements of CO and HCN. Due to the strong correlations with HCN and CO, the sources of organic aerosol are thought to be a combination of biomass burning, transportation and other urban combustion sources, and (pollution-related) secondary OA (SOA). High-resolution OA mass spectra were also analyzed with the Positive Matrix Factorization algorithm, including periods with high and low regional biomass burning (BB) as determined by satellite fire counts and tracers. Four dominant OA components were extracted. Three oxidized organic aerosol components, termed oxygenated OA 1 and 2 (OOA-1, OOA-2) and biomass burning OA (BBOA) were obtained, along with a reduced "hydrocarbon-like" (HOA) component. OOA-1 is linked to regional airmasses and highly oxidized and aged organic aerosol. Based on absolute levels and correlations with tracers in high vs. low fire periods, the majority (total to 2/3) attributed to anthropogenic sources and up to 1/3 estimated to come from BB during periods of high burning activity. OOA-2 appears to be a fresh SOA strongly correlated with ammonium nitrate, and the Mexico City Basin. The similar correlation with tracers in both flights strongly indicates an urban origin, and during low fires periods it is the largest OA component in the Mexico City basin. BBOA is identified as biomass burning aerosol due to a strong correlation with HCN, and the presence of marker ions such as C2H4O2+ and C3H5O2+ (m/z 60 and 73 markers for Levoglucosan). At times when burning activity is high, BBOA makes a large contribution to OA mass in the basin and contributes strongly to the mass in the outflow. This component is small (~10%) during periods of low BB activity. Comparing to measurements in the city basin (T0, Aiken et al., this conference) the BBOA observed in the C-130 has increased oxidation. This may be due to SOA formation from BB precursors, or to a Robinson-like evaporation-oxidation-repartitioning mechanism (Robinson et al., Science, 2007), since fresh BBOA in Mexico is very volatile (Huffman et al., this conference).
DE: 0305 Aerosols and particles (0345, 4801, 4906)
DE: 0345 Pollution: urban and regional (0305, 0478, 4251)
SC: Atmospheric Sciences [A]
MN: 2007 Fall Meeting