Measurements of tropospheric NO3 at midlatitude

被引:48
作者
Aliwell, SR [1 ]
Jones, RL [1 ]
机构
[1] Univ Cambridge, Ctr Atmospher Sci, Cambridge CB2 1EW, England
关键词
D O I
10.1029/97JD03119
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The column abundance of NO3 has been measured through sunrise at the midlatitude site of Cambridge, England. (52.2 degrees N, 0.1 degrees E) using zenith sky visible absorption spectroscopy. This technique allows distinction between the tropospheric and stratospheric components of the total NO3 vertical column during sunrise. Measurements of the tropospheric component during July to October 1995 are presented and show an average concentration of 89 ppt if it is assumed that all tropospheric NO3 is present in a 1 lan thick atmospheric boundary layer. The day today variability is considerable. The NO3 measurements together with point measurements of O-3, NO2, NO and temperature show that the NO3 lifetime is significantly longer than reported in other studies. The very short lifetime expected as a result of the measured levels of NO suggests that the ground level measurements of O-3, NO2 and NO are not representative of the whole boundary layer and therefore that the NO3 lifetime at the surface is not representative of the average boundary layer lifetime. Idealized model calculations confirm that a gradient in NO3 concentration would be expected in the boundary layer as a result of the different timescales for mixing and reaction with NO in a stable nocturnal situation. Any other rapid loss reaction near the surface, for example, with dimethyl sulphide in the marine environment or isoprene at a wooded rural site, may have a similar effect. In addition, such high concentrations of NO3 may alter the balance toward significant nighttime oxidation of hydrocarbons either directly or by production of OH.
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收藏
页码:5719 / 5727
页数:9
相关论文
共 20 条
[1]   Measurement of atmospheric NO3 .2. Diurnal variation of stratospheric NO3 at midlatitude [J].
Aliwell, SR ;
Jones, RL .
GEOPHYSICAL RESEARCH LETTERS, 1996, 23 (19) :2589-2592
[2]   Measurement of atmospheric NO3 .1. Improved removal of water vapour absorption features in the analysis for NO3 [J].
Aliwell, SR ;
Jones, RL .
GEOPHYSICAL RESEARCH LETTERS, 1996, 23 (19) :2585-2588
[3]  
ALIWELL SR, 1995, THESIS U CAMBRIDGE C
[4]   ESTIMATES OF ATMOSPHERIC HYDROXYL RADICAL CONCENTRATIONS FROM THE OBSERVED DECAY OF MANY REACTIVE HYDROCARBONS IN WELL-DEFINED URBAN PLUMES [J].
BLAKE, NJ ;
PENKETT, SA ;
CLEMITSHAW, KC ;
ANWYL, P ;
LIGHTMAN, P ;
MARSH, ARW ;
BUTCHER, G .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1993, 98 (D2) :2851-2864
[5]   Is the reaction between CH3C(O)O-2 and NO3 important in the night-time troposphere? [J].
CanosaMas, CE ;
King, MD ;
Lopez, R ;
Percival, CJ ;
Wayne, RP ;
Shallcross, DE ;
Pyle, JA ;
Daele, V .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (12) :2211-2222
[6]  
DEMORE WB, 1997, JPL PUB
[7]  
FISH DJ, 1994, THESIS U CAMBRIDGE C
[8]   Long-term observation of nitrate radicals at the tor station, Kap Arkona (Rugen) [J].
Heintz, F ;
Platt, U ;
Flentje, H ;
Dubois, R .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D17) :22891-22910
[9]   THE SEASONAL-VARIATION OF NONMETHANE HYDROCARBONS IN THE FREE TROPOSPHERE OVER THE NORTH-ATLANTIC OCEAN - POSSIBLE EVIDENCE FOR EXTENSIVE REACTION OF HYDROCARBONS WITH THE NITRATE RADICAL [J].
PENKETT, SA ;
BLAKE, NJ ;
LIGHTMAN, P ;
MARSH, ARW ;
ANWYL, P ;
BUTCHER, G .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1993, 98 (D2) :2865-2885
[10]  
Plane J. M. C., 1995, SPECTROSCOPY ENV SCI, P223