The influence of fog and airmass history on aerosol optical, physical and chemical properties at Pt. Reyes National Seashore

Carl M. Berkowitz, Larry K. Berg, Xiao Ying Yu, M. Lizabeth Alexander, Alexander Laskin, Rahul A. Zaveri, B. Thomas Jobson, Elisabeth Andrews, John A. Ogren

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17 Scopus citations

Abstract

This paper presents an analysis of the aerosol chemical composition, optical properties and size distributions for a range of conditions encountered during a field measurement campaign conducted between July 7-29, 2005 at Point Reyes National Seashore, north of San Francisco, CA. The fractional mass loading derived from hourly measurements of an Aerodyne Mass Spectrometer (AMS) during this period are compared with filter-pack measurements from the Pt. Reyes IMPROVE station with good agreement found between the two if it assumed that chloride is primarily from large sea-salt particles (not measured by the AMS). During the first half of the campaign (July 7-17), conditions at the site were largely maritime while flow during the second half of the campaigns (July 18-29) was influenced by a thermal trough that added a cyclonic twist to the incoming marine air, bringing it from the south with a more extensive over-land trajectory. Neither flow regime was associated with air coming from the San Francisco Bay area to the south. The AMS measurements are partitioned into clear and foggy conditions which are then used to calculate the equivalent molar ratio of ammonium to the sum of sulfate, nitrate and chloride. Ratios calculated from measurements made before the onset of the thermal trough on July 18th were associated with acidic or near-neutral particles. Measurements made after July 18th yield ratios that appear to have excess ammonium. Model calculations of the equilibrium gas-phase mixing ratio of NH3 suggest very high values which we attribute to agricultural practices within the park. Reported as an incidental finding is evidence for the cloud droplet activation of large particles (DP > 0.2 μm) with a corresponding reduction in the single scattering albedo of the non-activated particles, followed by a return in the particle size spectrum to the pre-fog conditions immediately afterwards.

Original languageEnglish
Pages (from-to)2559-2568
Number of pages10
JournalAtmospheric Environment
Volume45
Issue number15
DOIs
StatePublished - May 2011
Externally publishedYes

Funding

Financial support for this study was provided by the Atmospheric Sciences Program (now the Atmospheric Systems Research Program) of the Department of Energy’s Office of Biological and Environmental Research . The authors also gratefully acknowledge the NOAA Air Resources Laboratory (ARL) for the use of the HYSPLIT transport and dispersion model ( http://www.arl.noaa.gov/ready.html ) used in this publication, and to the Department of Energy’s Atmospheric Radiation Measurements Program for use of the observations collected by the ARM Mobile Facility during the campaign. Acknowledgment is also given to Brannon Ketcham and John DiGregoria of Pt. Reyes National Seashore who provided many useful comments on an early version of this manuscript, and to the anonymous reviewer who provided many constructive suggestions for how to improve the clarity of the manuscript. A portion of the research was performed using EMSL, a national scientific user facility sponsored by the Department of Energy’s Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory. PNNL is operated by the U.S. Department of Energy by Battelle Memorial Institute under contract DE-AC06-76RL0.

FundersFunder number
Office of Biological and Environmental Research
U.S. Department of Energy
BattelleDE-AC06-76RL0
Pacific Northwest National Laboratory

    Keywords

    • Aerodyne mass spectrometer
    • Air quality
    • Ammonia
    • Ammonium
    • Atmospheric aerosol
    • Dairy farm
    • IMPROVE
    • Pt. Reyes National Seashore
    • Scavenging
    • Sulfate
    • Thermal trough

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