Tunable diode laser measurements of formaldehyde during the TOPSE 2000 study: Distributions, trends, and model comparisons

被引:46
作者
Fried, A [1 ]
Wang, YH
Cantrell, C
Wert, B
Walega, J
Ridley, B
Atlas, E
Shetter, R
Lefer, B
Coffey, MT
Hannigan, J
Blake, D
Blake, N
Meinardi, S
Talbot, B
Dibb, J
Scheuer, E
Wingenter, O
Snow, J
Heikes, B
Ehhalt, D
机构
[1] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80303 USA
[2] Rutgers State Univ, Dept Environm Sci, New Brunswick, NJ 08903 USA
[3] Univ Colorado, Dept Chem, Boulder, CO 80309 USA
[4] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[5] Univ New Hampshire, Inst Study Earth Oceans & Space, Durham, NH 03824 USA
[6] New Mexico Inst Min & Technol, Dept Chem, Socorro, NM 87801 USA
[7] Univ Rhode Isl, Sch Oceanog, Narragansett, RI 02882 USA
[8] Inst Atmospher Chem, D-52428 Julich, Germany
关键词
airborne formaldehyde measurements; tunable diode laser measurements; formaldehyde measurements at high latitudes; formaldehyde during TOPSE;
D O I
10.1029/2002JD002208
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] Airborne measurements of formaldehyde (CH2O) were acquired employing tunable diode laser absorption spectroscopy (TDLAS) during the 2000 Tropospheric Ozone Production About the Spring Equinox (TOPSE) study. This study consisted of seven deployments spanning the time period from 4 February to 23 May 2000 and covered a wide latitudinal band from 40degreesN to 85degreesN. The median measured CH2O concentrations, with a few exceptions, did not show any clear temporal trends from February to May in each of five altitude and three latitude bins examined. Detailed measurement-model comparisons were carried out using a variety of approaches employing two different steady state models. Because recent emissions of CH2O and/or its precursors often result in model underpredictions, background conditions were identified using a number of chemical tracers. For background conditions at temperatures warmer than -45degreesC, the measurement-model agreement on average ranged between -13% and +5% (measurement-model/measurement), which corresponded to mean and median (measurement-model) differences of 3 +/- 69 and -6 parts per trillion by volume (pptv), respectively. At very low temperatures starting at around -45degreesC, significant and persistent (measurement-model) differences were observed from February to early April from southern Canada to the Arctic Ocean in the 6-8 km altitude range. In such cases, measured CH2O was as much as 392 pptv higher than modeled, and the median difference was 132 pptv (83%). Low light conditions as well as cold temperatures may be important in this effect. A number of possible mechanisms involving the reaction of CH3O2 with HO2 to produce CH2O directly were investigated, but in each case the discrepancy was only minimally reduced. Other possibilities were also considered but in each case there was no compelling evidence to support any of the hypotheses. Whatever the cause, the elevated CH2O concentrations significantly impact upper tropospheric HOx levels at high latitudes (>57degreesN) in the February-April time frame.
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页数:22
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