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Volume 16, issue 8
Atmos. Chem. Phys., 16, 5427-5451, 2016
https://doi.org/10.5194/acp-16-5427-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 16, 5427-5451, 2016
https://doi.org/10.5194/acp-16-5427-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 02 May 2016

Research article | 02 May 2016

Influences of emission sources and meteorology on aerosol chemistry in a polluted urban environment: results from DISCOVER-AQ California

Dominique E. Young1, Hwajin Kim1,a, Caroline Parworth1, Shan Zhou1, Xiaolu Zhang2, Christopher D. Cappa2, Roger Seco3, Saewung Kim3, and Qi Zhang1 Dominique E. Young et al.
  • 1Department of Environmental Toxicology, University of California, Davis, CA 95616, USA
  • 2Department of Civil and Environmental Engineering, University of California, Davis, CA 95616, USA
  • 3Department of Earth System Science, University of California, Irvine, CA 92697, USA
  • anow at: Center for Environment, Health and Welfare Research, Korea Institute Science and Technology, Seoul, Korea

Abstract. The San Joaquin Valley (SJV) in California experiences persistent air-quality problems associated with elevated particulate matter (PM) concentrations due to anthropogenic emissions, topography, and meteorological conditions. Thus it is important to unravel the various sources and processes that affect the physicochemical properties of PM in order to better inform pollution abatement strategies and improve parameterizations in air-quality models.

During January and February 2013, a ground supersite was installed at the Fresno–Garland California Air Resources Board (CARB) monitoring station, where comprehensive, real-time measurements of PM and trace gases were performed using instruments including an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) and an Ionicon proton transfer reaction time-of-flight mass spectrometer (PTR-TOF-MS) as part of the NASA Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) campaign. The average submicron aerosol (PM1) concentration was 31.0µgm−3 and the total mass was dominated by organic aerosols (OA, 55%), followed by ammonium nitrate (35%). High PM pollution events were commonly associated with elevated OA concentrations, mostly from primary sources. Organic aerosols had average atomic oxygen-to-carbon (O/C), hydrogen-to-carbon (H/C), and nitrogen-to-carbon (N/C) ratios of 0.42, 1.70, and 0.017, respectively. Six distinct sources of organic aerosol were identified from positive matrix factorization (PMF) analysis of the AMS data: hydrocarbon-like OA (HOA; 9% of total OA, O/C = 0.09) associated with local traffic, cooking OA (COA; 18% of total OA, O/C = 0.19) associated with food cooking activities, two biomass burning OA (BBOA1: 13% of total OA, O/C = 0.33; BBOA2: 20% of total OA, O/C = 0.60) most likely associated with residential space heating from wood combustion, and semivolatile oxygenated OA (SV-OOA; 16% of total OA, O/C = 0.63) and low-volatility oxygenated OA (LV-OOA; 24% of total OA, O/C = 0.90) formed via chemical reactions in the atmosphere.

Large differences in aerosol chemistry at Fresno were observed between the current campaign (winter 2013) and a previous campaign in winter 2010, most notably that PM1 concentrations were nearly 3 times higher in 2013 than in 2010. These variations were attributed to differences in the meteorological conditions, which influenced primary emissions and secondary aerosol formation. In particular, COA and BBOA concentrations were greater in 2013 than 2010, where colder temperatures in 2013 likely resulted in increased biomass burning activities. The influence from a nighttime formed residual layer that mixed down in the morning was found to be much more intense in 2013 than 2010, leading to sharp increases in ground-level concentrations of secondary aerosol species including nitrate, sulfate, and OOA, in the morning between 08:00 and 12:00PST. This is an indication that nighttime chemical reactions may have played a more important role in 2013. As solar radiation was stronger in 2013 the higher nitrate and OOA concentrations in 2013 could also be partly due to greater photochemical production of secondary aerosol species. The greater solar radiation and larger range in temperature in 2013 also likely led to both SV-OOA and LV-OOA being observed in 2013 whereas only a single OOA factor was identified in 2010.

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Aerosol chemistry and the sources and processes driving the observed temporal and diurnal variations of PM were studied in a polluted urban environment during winter 2013. These results were compared to a similar campaign from winter 2010. Meteorology strongly influenced PM composition, both directly and indirectly. Nighttime reactions played a more important role in 2013 and the influence from a nighttime formed residual layer that mixed down in the morning was also much more intense in 2013.
Aerosol chemistry and the sources and processes driving the observed temporal and diurnal...
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