Organic composition of single and submicron particles in different regions of western North America and the eastern Pacific during INTEX-B 2006

被引:19
作者
Day, D. A. [1 ]
Takahama, S. [1 ]
Gilardoni, S. [1 ]
Russell, L. M. [1 ]
机构
[1] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
关键词
AEROSOL MASS-SPECTROMETRY; UNITED-STATES; CARBONACEOUS AEROSOLS; ATMOSPHERIC PARTICLES; CHEMICAL-COMPOSITION; FUNCTIONAL-GROUPS; MEXICO-CITY; CLIMATE; SECONDARY; URBAN;
D O I
10.5194/acp-9-5433-2009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Single particles were collected from an aircraft platform as part of the Intercontinental Chemical Transport Experiment - Phase B (INTEX-B) conducted over the eastern Pacific and western North America. Single particle spectra were obtained using scanning transmission X-ray microscopy-near edge X-ray absorption fine structure spectroscopy (STXM-NEXAFS). Bulk submicron particles were also collected and organic functional group and elemental concentrations were quantified with Fourier transform infrared (FTIR) spectroscopy and X-ray fluorescence (XRF). Single particle spectra were classified into metaclasses associated with different sources and atmospheric processing. Particles with spectra indicative of secondary organic aerosol production and combustion sources were found at several locations and a range of altitudes. At lower altitudes, particles with spectra resembling soil dust and biomass burning fingerprints were commonly observed. The types of particle spectra most commonly observed aloft were similar to those observed during a previous study over the northwestern Pacific, indicating that long-range transport may have been an important particle source. Single particle spectra provided evidence that condensation and surface-limited oxidation contributed to particle growth. Organic mass (OM) concentrations ranged from 1 to 7 mu g m(-3) and averaged 2.4-4.1 mu g m(-3). Alkane functional groups were the largest fraction of OM, averaging 1.9-2.1 mu g m(-3) or 50-76% of OM, followed by alcohol functional groups (0.35-0.39 mu g m(-3), 9-14%). Organic and elemental concentrations are compared within and among geographical air mass regions: 'Pacific' free troposphere, 'Continental' free troposphere, 'Seattle' metropolitan region, and the California 'Central Valley'. OM concentrations were highest and most variable in the Central Valley (3.5 +/- 2 mu g m(-3)). Oxygen-to-carbon ratios were relatively constant in the Central Valley but variable for the Continental air masses. Overall, the OM concentrations showed greater variability within air mass categories as compared to averages among them, suggesting sampled air mass regions included a variety of sources and processing of organic aerosol.
引用
收藏
页码:5433 / 5446
页数:14
相关论文
共 39 条
[1]  
Ade H., 2002, ADV SERIES PHYS CHEM, V12A, P285
[2]   O/C and OM/OC ratios of primary, secondary, and ambient organic aerosols with high-resolution time-of-flight aerosol mass spectrometry [J].
Aiken, Allison C. ;
Decarlo, Peter F. ;
Kroll, Jesse H. ;
Worsnop, Douglas R. ;
Huffman, J. Alex ;
Docherty, Kenneth S. ;
Ulbrich, Ingrid M. ;
Mohr, Claudia ;
Kimmel, Joel R. ;
Sueper, Donna ;
Sun, Yele ;
Zhang, Qi ;
Trimborn, Achim ;
Northway, Megan ;
Ziemann, Paul J. ;
Canagaratna, Manjula R. ;
Onasch, Timothy B. ;
Alfarra, M. Rami ;
Prevot, Andre S. H. ;
Dommen, Josef ;
Duplissy, Jonathan ;
Metzger, Axel ;
Baltensperger, Urs ;
Jimenez, Jose L. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (12) :4478-4485
[3]   Characterization of urban and rural organic particulate in the lower Fraser valley using two aerodyne aerosol mass spectrometers [J].
Alfarra, MR ;
Coe, H ;
Allan, JD ;
Bower, KN ;
Boudries, H ;
Canagaratna, MR ;
Jimenez, JL ;
Jayne, JT ;
Garforth, AA ;
Li, SM ;
Worsnop, DR .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (34) :5745-5758
[4]   Climatology of PM2.5 organic carbon concentrations from a review of ground-based atmospheric measurements by evolved gas analysis [J].
Bahadur, Ranjit ;
Habib, Gazala ;
Russell, Lynn M. .
ATMOSPHERIC ENVIRONMENT, 2009, 43 (09) :1591-1602
[5]   Carbon speciation in airborne particulate matter with C (1s) NEXAFS spectroscopy [J].
Braun, A .
JOURNAL OF ENVIRONMENTAL MONITORING, 2005, 7 (11) :1059-1065
[6]   Global distribution and climate forcing of carbonaceous aerosols [J].
Chung, SH ;
Seinfeld, JH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D19) :AAC14-1
[7]   INDOEX aerosol: A comparison and summary of chemical, microphysical, and optical properties observed from land, ship, and aircraft [J].
Clarke, AD ;
Howell, S ;
Quinn, PK ;
Bates, TS ;
Ogren, JA ;
Andrews, E ;
Jefferson, A ;
Massling, A ;
Mayol-Bracero, O ;
Maring, H ;
Savoie, D ;
Cass, G .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D19)
[8]   Aerosol chemical composition and distribution during the Pacific Exploratory Mission (PEM) Tropics [J].
Dibb, JE ;
Talbot, RW ;
Scheuer, EM ;
Blake, DR ;
Blake, NJ ;
Gregory, GL ;
Sachse, GW ;
Thornton, DC .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D5) :5785-5800
[9]   Evolution of Asian aerosols during transpacific transport in INTEX-B [J].
Dunlea, E. J. ;
DeCarlo, P. F. ;
Aiken, A. C. ;
Kimmel, J. R. ;
Peltier, R. E. ;
Weber, R. J. ;
Tomlinson, J. ;
Collins, D. R. ;
Shinozuka, Y. ;
McNaughton, C. S. ;
Howell, S. G. ;
Clarke, A. D. ;
Emmons, L. K. ;
Apel, E. C. ;
Pfister, G. G. ;
van Donkelaar, A. ;
Martin, R. V. ;
Millet, D. B. ;
Heald, C. L. ;
Jimenez, J. L. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2009, 9 (19) :7257-7287
[10]   Regional variation of organic functional groups in aerosol particles on four US east coast platforms during the International Consortium for Atmospheric Research on Transport and Transformation 2004 campaign [J].
Gilardoni, S. ;
Russell, L. M. ;
Sorooshian, A. ;
Flagan, R. C. ;
Seinfeld, J. H. ;
Bates, T. S. ;
Quinn, P. K. ;
Allan, J. D. ;
Williams, B. ;
Goldstein, A. H. ;
Onasch, T. B. ;
Worsnop, D. R. .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2007, 112 (D10)