Peroxy radical observations using chemical ionization mass spectrometry during TOPSE

被引:31
作者
Cantrell, CA
Edwards, GD
Stephens, S
Mauldin, L
Kosciuch, E
Zondlo, M
Eisele, F
机构
[1] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80303 USA
[2] Georgia Inst Technol, Atlanta, GA 30332 USA
关键词
peroxy radicals; tropospheric photochemistry; chemical ionization mass spectrometry; hydroperoxyl radical; organylperoxyl radical; TOPSE;
D O I
10.1029/2002JD002715
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] Peroxy radicals (HO2 + RO2) were measured by chemical conversion-chemical ionization mass spectroscopy in the TOPSE (Tropospheric Ozone Production about the Spring Equinox) campaign that took place February through May 2000. Instrumentation for these measurements was deployed on the NCAR/NSF C-130 aircraft that flew at latitudes from 40 to 85 degreesN, and altitudes from the surface to 7.5 km over the North American continent. The measurements demonstrate the evolution of photochemical activity as time progresses through the study period due to increases in free radical source rates. The increase in average peroxy radical concentration moves northward as the maximum solar elevation and length of sunlit days increase. HOxROx (HO2 + RO2) concentrations are distributed lognormally with means of 11.5 and 7.8 pptv for the middle-latitude band (MLB) and high-latitude band (HLB), respectively. The observations agree well on average with steady state derived concentrations; measurement-model concentration ratios are 1.04 (MLB) and 0.94 (HLB). Concentrations within a given latitude band and altitude region sometimes appear to increase with NOx concentrations, but this correlation nearly disappears at low and moderate NOx levels when the data are parsed by radical production rate; lower radical levels are observed at the highest NOx levels measured (near 1 ppbv). These data are compared with results from other recent observations utilizing a variety of platforms.
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