Gas and aerosol carbon in California: comparison of measurements and model predictions in Pasadena and Bakersfield

被引:38
作者
Baker, K. R. [1 ]
Carlton, A. G. [2 ]
Kleindienst, T. E. [3 ]
Offenberg, J. H. [3 ]
Beaver, M. R. [3 ]
Gentner, D. R. [4 ]
Goldstein, A. H. [5 ]
Hayes, P. L. [6 ]
Jimenez, J. L. [7 ,8 ]
Gilman, J. B. [9 ]
de Gouw, J. A. [9 ]
Woody, M. C. [3 ]
Pye, H. O. T. [3 ]
Kelly, J. T. [1 ]
Lewandowski, M. [3 ]
Jaoui, M. [10 ]
Stevens, P. S. [11 ,12 ]
Brune, W. H. [13 ]
Lin, Y. -H. [14 ]
Rubitschun, C. L. [14 ]
Surratt, J. D. [14 ]
机构
[1] US EPA, Off Air Qual Planning & Stand, Res Triangle Pk, NC 27711 USA
[2] Rutgers State Univ, Dept Environm Sci, New Brunswick, NJ 08903 USA
[3] US EPA, Off Res & Dev, Res Triangle Pk, NC 27711 USA
[4] Yale Univ, Dept Chem & Environm Engn, New Haven, CT USA
[5] Univ Calif Berkeley, Dept Civil & Environm Engn, Berkeley, CA 94720 USA
[6] Univ Montreal, Dept Chim, Montreal, PQ H3C 3J7, Canada
[7] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
[8] Univ Colorado, CIRES, Boulder, CO 80309 USA
[9] Natl Ocean & Atmospher Adm, Chem Sci Div, Earth Syst Res Lab, Boulder, CO USA
[10] Alion Sci & Technol Inc, Res Triangle Pk, NC USA
[11] Indiana Univ, Sch Publ & Environm Affairs, Ctr Res Environm Sci, Bloomington, IN USA
[12] Indiana Univ, Dept Chem, Bloomington, IN USA
[13] Penn State Univ, Dept Meteorol, University Pk, PA 16802 USA
[14] Univ N Carolina, Dept Environm Sci & Engn, Gillings Sch Global Publ Hlth, Chapel Hill, NC USA
关键词
SECONDARY ORGANIC AEROSOL; SAN-JOAQUIN VALLEY; AIR-QUALITY; LOS-ANGELES; AGRICULTURAL CROPS; OXALIC-ACID; 2010; CALNEX; EMISSIONS; SOA; OXIDATION;
D O I
10.5194/acp-15-5243-2015
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Co-located measurements of fine particulate matter (PM2.5 /organic carbon (OC), elemental carbon, radiocarbon (C-14), speciated volatile organic compounds (VOCs), and OH radicals during the CalNex field campaign provide a unique opportunity to evaluate the Community Multi-scale Air Quality (CMAQ) model's representation of organic species from VOCs to particles. Episode average daily 23 h average C-14 analysis indicates PM2.5 carbon at Pasadena and Bakersfield during the CalNex field campaign was evenly split between contemporary and fossil origins. CMAQ predicts a higher contemporary carbon fraction than indicated by the C-14 analysis at both locations. The model underestimates measured PM2.5 organic carbon at both sites with very little (7% in Pasadena) of the modeled mass represented by secondary production, which contrasts with the ambient-based SOC / OC fraction of 63% at Pasadena. Measurements and predictions of gas-phase anthropogenic species, such as toluene and xylenes, are generally within a factor of 2, but the corresponding SOC tracer (2,3-dihydroxy-4-oxo-pentanoic acid) is systematically underpredicted by more than a factor of 2. Monoterpene VOCs and SOCs are underestimated at both sites. Isoprene is underestimated at Pasadena and overpredicted at Bakersfield and isoprene SOC mass is underestimated at both sites. Systematic model underestimates in SOC mass coupled with reasonable skill (typically within a factor of 2) in predicting hydroxyl radical and VOC gas-phase precursors suggest error( s) in the parameterization of semivolatile gases to form SOC. Yield values (alpha) applied to semivolatile partitioning species were increased by a factor of 4 in CMAQ for a sensitivity simulation, taking into account recent findings of underestimated yields in chamber experiments due to gas wall losses. This sensitivity resulted in improved model performance for PM2.5 organic carbon at both field study locations and at routine monitor network sites in California. Modeled percent secondary contribution (22% at Pasadena) becomes closer to ambient-based estimates but still contains a higher primary fraction than observed.
引用
收藏
页码:5243 / 5258
页数:16
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