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Ammonia and ammonium measurements from the southeastern United States
Institution:1. Atmospheric Research & Analysis, Inc., 410 Midenhall Way, Cary, NC 27513, USA;2. Atmospheric Research & Analysis, Inc., Snellville, GA, USA;3. Atmospheric Research & Analysis, Inc., Plano, TX, USA;4. Southern Company, Birmingham, AL, USA;5. Electric Power Research Institute, Palo Alto, CA, USA;1. Instituto de Investigaciones Agropecuarias INIA, Carretera Panamericana Sur km 8 Norte, Osorno, Chile;2. Rothamsted Research, North Wyke, Okehampton, Devon EX20 2SB, UK;1. Centre for Ecology & Hydrology Edinburgh, Bush Estate, Penicuik, Midlothian EH26 0QB, UK;2. Rothamsted Research, North Wyke, Okehampton, Devon EX20 2SB, UK;1. Key Laboratory for Ultrafine Materials of Ministry of Education, School of Material Science and Engineering, East China University of Science and Technology, Shanghai 200237, PR China;2. School of Biomedical Engineering, Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, 200030, PR China;1. University of Potsdam, Dept. of Ecology and Ecosystem Modelling, Maulbeerallee 2, 14469 Potsdam, Germany;2. University of Potsdam, Dept. of Theoretical Aquatic Ecology and Ecophysiology, Maulbeerallee 2, 14469 Potsdam, Germany;1. Department of Environmental Horticulture, Dankook University, Cheonan, Chungnam 330-714, Korea;2. US Department of Agriculture, Agricultural Research Service, Floral and Nursery Plants Research Unit, Beltsville, MD 20705, USA
Abstract:Twenty-four-hour integrated gaseous NH3 and fine particulate (PM2.5)NH4+ were measured during 2004 at eight sites in the southeastern U.S. Mean NH3 concentrations for 2004 ranged from 2.44 ppbv at an urban-industrial site in North Birmingham, AL, to 0.23 ppbv at a rural-forested site near Centreville, AL. NH3 mixing ratios were found to be higher at urban sites than at nearby rural (or suburban sites) except for sites which were directly influenced by local sources. Only weak correlations with temperature were observed for NH3 at the sites; slightly greater correlations were observed for total ammonia (NHx=NH3+NH4+) vs. temperature. A weak seasonal variation was observed for NH3 mixing ratios at all sites, with all but one site exhibiting biannual maxima in spring and late summer/fall. Mean PM2.5 NH4+ concentrations ranged from 1.78μgm-3 in Atlanta, GA, to 1.02μgm-3 at Oak Grove, MS, and were more uniform across the network than NH3 mixing ratios, with only slightly larger values at urban sites as compared to nearby rural (or suburban) sites. All sites exhibited highest NHx between July and September and lowest NHx in November and December. The gaseous NH3 fraction (NH3/(NH3+NH4+)) was observed to decrease with increasing values of PM2.5 SO42- at all sites. At two rural-forested sites and two sites near the Gulf of Mexico, the NH3 gaseous fraction approached a relatively constant value of 5–10% as PM2.5SO42- increased beyond 5–7μgm-3, suggesting that NH3 availability at these locations limits aerosol neutralization.
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