Interaction between nitrogen and sulfur cycles in the polluted marine boundary layer
Author(s) -
Yvon S. A.,
Plane J. M. C.,
Nien C.F.,
Cooper D. J.,
Saltzman E. S.
Publication year - 1996
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 - 10.1029/95jd02905
Subject(s) - sink (geography) , boundary layer , nitrogen , ozone , environmental science , bay , nox , nitrogen dioxide , planetary boundary layer , nitrate , atmospheric sciences , sulfur , oceanography , sulfur dioxide , environmental chemistry , chemistry , meteorology , geology , inorganic chemistry , thermodynamics , combustion , physics , geography , cartography , organic chemistry
Simultaneous measurements are reported of the nitrate radical (NO 3 ), nitrogen dioxide (NO 2 ), ozone (O 3 ), and dimethylsulfide (DMS) in the nighttime marine boundary layer over Biscayne Bay in South Florida. These field observations are analyzed and used to initialize a boundary layer box model which examines the relative importance of the various sinks for NO x in the marine boundary layer. The results show that the observed lifetime of NO 3 (≤6 min.) is probably controlled both by the loss of nitrogen pentoxide (N 2 O 5 ) to reaction with water vapor and aerosols and by the reaction between NO 3 and DMS. The model is then extended to investigate the loss of nitrogen oxides from an air parcel that remains in the boundary layer with a constant sea‐to‐air DMS flux for several days. The principal conclusions are (1) that DMS is a much more important sink for NO 3 at lower NO 2 levels and (2) that the reaction between NO 3 and DMS is an important sink for DMS in the marine boundary layer and could exceed that of the daytime removal by OH.
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