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Aerosol major ion record at Mount Washington
Author(s) -
Fischer E. V.,
Ziemba L. D.,
Talbot R. W.,
Dibb J. E.,
Griffin R. J.,
Husain L.,
Grant A. N.
Publication year - 2007
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2006jd007253
Subject(s) - environmental science , aerosol , spring (device) , atmospheric sciences , seasonality , air mass (solar energy) , climatology , meteorology , geography , geology , ecology , mechanical engineering , physics , boundary layer , engineering , biology , thermodynamics
This study examined the seasonal cycles and regional‐scale meteorological controls on the chemical properties of bulk aerosols collected from 1999 to 2004 at Mount Washington, the highest peak in the northeastern United States. The concentrations of NH 4 + and SO 4 2− peaked during summer months. The pattern for aerosol NO 3 − was more complicated with relatively high median concentrations characterizing spring and summer months, but with major elevated events occurring during fall, winter, and spring. The seasonal relationship between NH 4 + and SO 4 2− indicated that during warmer months a mixture of (NH 4 ) 2 SO 4 and NH 4 HSO 4 was present, while it was mainly the latter in winter. More acidity and higher concentrations of the major species were generally associated with winds from the southwest and west sectors. The highest (≥95th percentile) concentrations of SO 4 2− and NH 4 + were associated with air mass transport from major upwind source regions in the Midwest and along the eastern seaboard. The ionic composition and seasonal cycle observed at Mount Washington were similar to those measured at other northeastern sites, but the range and average concentrations were much lower. These differences were exaggerated during wintertime. Included in this paper are several Eulerian case studies of SO 2 conversion to SO 4 2− during transit from Whiteface Mountain, New York, to Mount Washington. The calculations suggest a gas‐phase SO 2 oxidation rate of ∼1–2% per hour and demonstrate the possibility of using these two sites to investigate the chemical evolution of air masses as they move from Midwestern source regions to northern New England.

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