Variability in nocturnal nitrogen oxide processing and its role in regional air quality

被引:320
作者
Brown, SS
Ryerson, TB
Wollny, AG
Brock, CA
Peltier, R
Sullivan, AP
Weber, RJ
Dubé, WP
Trainer, M
Meagher, JF
Fehsenfeld, FC
Ravishankara, AR
机构
[1] NOAA, Earth Syst Res Lab, Boulder, CO 80305 USA
[2] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[3] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
[4] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
关键词
D O I
10.1126/science.1120120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nitrogen oxides in the lower troposphere catalyze the photochemical production of ozone (O-3) pollution during the day but react to form nitric acid, oxidize hydrocarbons, and remove O-3 at night. A key nocturnal reaction is the heterogeneous hydrolysis of dinitrogen pentoxide, N2O5. We report aircraft measurements of NO3 and N2O5, which show that the N2O5 uptake coefficient, gamma(N2O5), on aerosol particles is highly variable and depends strongly on aerosol composition, particularly sulfate content. The results have implications for the quantification of regional-scale O-3 production and suggest a stronger interaction between anthropogenic sulfur and nitrogen oxide emissions than previously recognized.
引用
收藏
页码:67 / 70
页数:4
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