Quantifying wet scavenging processes in aircraft observations of nitric acid and cloud condensation nuclei

被引:32
作者
Garrett, T. J.
Avey, L.
Palmer, P. I.
Stohl, A.
Neuman, J. A.
Brock, C. A.
Ryerson, T. B.
Holloway, J. S.
机构
[1] Univ Utah, Dept Meteorol, Salt Lake City, UT 84112 USA
[2] Univ Leeds, Sch Earth & Environm, Leeds LS2 9JT, W Yorkshire, England
[3] Norsk Inst Luftforskning, N-2027 Kjeller, Norway
[4] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[5] NOAA, Div Chem Sci, Earth Syst Res Lab, Boulder, CO 80305 USA
关键词
D O I
10.1029/2006JD007416
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[ 1] Wet scavenging is an important sink term for many atmospheric constituents. However, production of precipitation in clouds is poorly understood, and pollutant removal through wet scavenging is difficult to separate from removal through dry scavenging, atmospheric mixing, or chemical transformations. Here we use airborne data from the International Consortium for Atmospheric Research on Transport and Transformation project to show that measured ratios of soluble and insoluble trace gases provide a useful indicator for quantifying wet scavenging. Specifically, nitric acid (HNO3), produced as a by-product of combustion, is highly soluble and removed efficiently from clouds by rain. Regional carbon monoxide ( CO), which is also an indicator of anthropogenic activity, is insoluble and has a lifetime against oxidation of about a month. We find that relative concentrations of HNO3 to regional CO observed in clear air are negatively correlated with precipitation production rates in nearby cloudy air (r(2) = 0.85). Also, we show that relative concentrations of HNO3 and CO can be used to quantify cloud condensation nucleus (CCN) scavenging by precipitating clouds. This is because CCN and HNO3 molecules are both fully soluble in cloud water and hence can be treated as analogous species insofar as wet scavenging is concerned. While approximate, the practical advantage of this approach to scavenging studies is that it requires only measurement in clear air and no a priori knowledge of the cloud or aerosol properties involved.
引用
收藏
页数:12
相关论文
共 51 条
[1]   REASSESSING THE DEPENDENCE OF CLOUD CONDENSATION NUCLEUS CONCENTRATION ON FORMATION RATE [J].
ACKERMAN, AS ;
TOON, OB ;
HOBBS, PV .
NATURE, 1994, 367 (6462) :445-447
[2]   Disproportionate impact of particulate emissions on global cloud condensation nuclei concentrations [J].
Adams, PJ ;
Seinfeld, JH .
GEOPHYSICAL RESEARCH LETTERS, 2003, 30 (05)
[3]   AEROSOLS, CLOUD MICROPHYSICS, AND FRACTIONAL CLOUDINESS [J].
ALBRECHT, BA .
SCIENCE, 1989, 245 (4923) :1227-1230
[4]   Estimates of sulfate aerosol wet scavenging coefficient for locations in the Eastern United States [J].
Andronache, C .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (06) :795-804
[5]   Estimated variability of below-cloud aerosol removal by rainfall for observed aerosol size distributions [J].
Andronache, C .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2003, 3 :131-143
[6]   PARAMETERIZATION OF BELOW-CLOUD SCAVENGING OF HIGHLY SOLUBLE GASES UNDER CONVECTIVE CONDITIONS [J].
ASMAN, WAH .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (12) :1359-1368
[7]   BISTABILITY OF CCN CONCENTRATIONS AND THERMODYNAMICS IN THE CLOUD-TOPPED BOUNDARY-LAYER [J].
BAKER, MB ;
CHARLSON, RJ .
NATURE, 1990, 345 (6271) :142-145
[8]   Evidence for the formation of CCN by photochemical processes in Mexico City [J].
Baumgardner, D ;
Raga, GB ;
Muhlia, A .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (03) :357-367
[9]   THE SOLUBILITY AND BEHAVIOR OF ACID GASES IN THE MARINE AEROSOL [J].
BRIMBLECOMBE, P ;
CLEGG, SL .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1988, 7 (01) :1-18
[10]   Particle characteristics following cloud-modified transport from Asia to North America -: art. no. D23S26 [J].
Brock, CA ;
Hudson, PK ;
Lovejoy, ER ;
Sullivan, A ;
Nowak, JB ;
Huey, LG ;
Cooper, OR ;
Cziczo, DJ ;
de Gouw, J ;
Fehsenfeld, FC ;
Holloway, JS ;
Hübler, G ;
Lafleur, BG ;
Murphy, DM ;
Neuman, JA ;
Nicks, DK ;
Orsini, DA ;
Parrish, DD ;
Ryerson, TB ;
Tanner, DJ ;
Warneke, C ;
Weber, RJ ;
Wilson, JC .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D23) :1-17