TY - JOUR
T1 - Air quality diagnosis from comprehensive observations of total OH reactivity and reactive trace species in urban central Tokyo
AU - Yoshino, Ayako
AU - Nakashima, Yoshihiro
AU - Miyazaki, Koji
AU - Kato, Shungo
AU - Suthawaree, Jeeranut
AU - Shimo, Nobuo
AU - Matsunaga, Sou
AU - Chatani, Satoru
AU - Apel, Eric
AU - Greenberg, James
AU - Guenther, Alex
AU - Ueno, Hiroyuki
AU - Sasaki, Hiroyuki
AU - Hoshi, Jun ya
AU - Yokota, Hisashi
AU - Ishii, Koichiro
AU - Kajii, Yoshizumi
PY - 2012/3
Y1 - 2012/3
N2 - We have conducted a comprehensive observational study to determine the mixing ratios of atmospheric chemical species and total OH reactivity in central Tokyo, in order to diagnose the air quality during summer and winter 2007 and autumn 2009. Concentrations of over 70 reactive trace species were continuously measured throughout each season. The total OH reactivity was measured directly using a laser-induced pump and probe technique. The observed chemical species exhibited seasonal variations. There was a good correlation between NO and CO in winter, but not in summer. This indicates that during winter, vehicle exhaust provided a significant source of NO in central Tokyo, while photolysis of NO 2 was dominant in summer. Similar values (approximately 30s -1) for the averaged total OH reactivity were observed in both summer and autumn during the daytime. However, VOCs accounted for a larger percentage of the OH reactivity in summer, while NO x was more dominant in autumn. We find that photochemical processes leading to oxidant production via VOCs dominated OH removal in summer, while the production of nitric acid from the reaction between OH and NO 2 was dominant in autumn, by-passing the oxidant production pathways and resulting in reduced oxidant formation.
AB - We have conducted a comprehensive observational study to determine the mixing ratios of atmospheric chemical species and total OH reactivity in central Tokyo, in order to diagnose the air quality during summer and winter 2007 and autumn 2009. Concentrations of over 70 reactive trace species were continuously measured throughout each season. The total OH reactivity was measured directly using a laser-induced pump and probe technique. The observed chemical species exhibited seasonal variations. There was a good correlation between NO and CO in winter, but not in summer. This indicates that during winter, vehicle exhaust provided a significant source of NO in central Tokyo, while photolysis of NO 2 was dominant in summer. Similar values (approximately 30s -1) for the averaged total OH reactivity were observed in both summer and autumn during the daytime. However, VOCs accounted for a larger percentage of the OH reactivity in summer, while NO x was more dominant in autumn. We find that photochemical processes leading to oxidant production via VOCs dominated OH removal in summer, while the production of nitric acid from the reaction between OH and NO 2 was dominant in autumn, by-passing the oxidant production pathways and resulting in reduced oxidant formation.
KW - Total OH reactivity
KW - Tropospheric ozone
KW - Urban air quality
KW - Volatile organic compounds
UR - https://www.scopus.com/pages/publications/84856533517
U2 - 10.1016/j.atmosenv.2011.12.029
DO - 10.1016/j.atmosenv.2011.12.029
M3 - Article
AN - SCOPUS:84856533517
SN - 1352-2310
VL - 49
SP - 51
EP - 59
JO - Atmospheric Environment
JF - Atmospheric Environment
ER -