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Modeling NH4NO3 Over the San Joaquin Valley During the 2013 DISCOVER-AQ Campaign.
Kelly, James T; Parworth, Caroline L; Zhang, Qi; Miller, David J; Sun, Kang; Zondlo, Mark A; Baker, Kirk R; Wisthaler, Armin; Nowak, John B; Pusede, Sally E; Cohen, Ronald C; Weinheimer, Andrew J; Beyersdorf, Andreas J; Tonnesen, Gail S; Bash, Jesse O; Valin, Luke C; Crawford, James H; Fried, Alan; Walega, James G.
Afiliación
  • Kelly JT; Office of Air Quality Planning and Standards, U.S. Environmental Protection Agency, RTP, NC, USA.
  • Parworth CL; Ames Research Center, National Aeronautics and Space Administration, Moffett Field, CA, USA.
  • Zhang Q; Department of Environmental Toxicology, University of California, Davis, CA, USA.
  • Miller DJ; Agricultural and Environmental Chemistry Graduate Group, University of California, Davis, CA, USA.
  • Sun K; Environmental Defense Fund, Boston, MA, USA.
  • Zondlo MA; Atomic and Molecular Physics Division, Harvard-Smithsonian Center for Astrophysics, Cambridge, MA, USA.
  • Baker KR; Department of Civil and Environmental Engineering, Princeton University, Princeton, NJ, USA.
  • Wisthaler A; Office of Air Quality Planning and Standards, U.S. Environmental Protection Agency, RTP, NC, USA.
  • Nowak JB; Institute for Ion Physics and Applied Physics, University of Innsbruck, Innsbruck, Austria.
  • Pusede SE; Langley Research Center, National Aeronautics and Space Administration, Hampton, VA, USA.
  • Cohen RC; Department of Environmental Sciences, University of Virginia, Charlottesville, VA, USA.
  • Weinheimer AJ; Department of Earth and Planetary Sciences, University of California at Berkeley, Berkeley, CA, USA.
  • Beyersdorf AJ; National Center for Atmospheric Research, Boulder, CO, USA.
  • Tonnesen GS; Department of Chemistry and Biochemistry, California State University, San Bernardino, CA, USA.
  • Bash JO; Region 8, U.S. Environmental Protection Agency, Denver, CO, USA.
  • Valin LC; Office of Research and Development, U.S. Environmental Protection Agency, RTP, NC, USA.
  • Crawford JH; Office of Research and Development, U.S. Environmental Protection Agency, RTP, NC, USA.
  • Fried A; Langley Research Center, National Aeronautics and Space Administration, Hampton, VA, USA.
  • Walega JG; Institute of Arctic and Alpine Research, University of Colorado Boulder, Boulder, CO, USA.
J Geophys Res Atmos ; 123(9): 4727-4745, 2018 May 16.
Article en En | MEDLINE | ID: mdl-30245954
ABSTRACT
The San Joaquin Valley (SJV) of California experiences high concentrations of particulate matter NH4NO3 during episodes of meteorological stagnation in winter. A rich data set of observations related to NH4NO3 formation was acquired during multiple periods of elevated NH4NO3 during the Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) field campaign in SJV in January and February 2013. Here NH4NO3 is simulated during the SJV DISCOVER-AQ study period with the Community Multiscale Air Quality (CMAQ) model, diagnostic model evaluation is performed using the DISCOVER-AQ data set, and integrated reaction rate analysis is used to quantify HNO3 production rates. Simulated NO3- generally agrees well with routine monitoring of 24-hr average NO3-, but comparisons with hourly average NO3- measurements in Fresno revealed differences at higher time resolution. Predictions of gas-particle partitioning of total nitrate (HNO3 + NO3-) and NHx (NH3 + NH4+) generally agree well with measurements in Fresno, although partitioning of total nitrate to HNO3 is sometimes overestimated at low relative humidity in afternoon. Gas-particle partitioning results indicate that NH4NO3 formation is limited by HNO3 availability in both the model and ambient. NH3 mixing ratios are underestimated, particularly in areas with large agricultural activity, and additional work on the spatial allocation of NH3 emissions is warranted. During a period of elevated NH4NO3, the model predicted that the OH + NO2 pathway contributed 46% to total HNO3production in SJV and the N2O5 heterogeneous hydrolysis pathway contributed 54%. The relative importance of the OH + NO2 pathway for HNO3 production is predicted to increase as NOx emissions decrease.

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Geophys Res Atmos Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Geophys Res Atmos Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos