Chemical NOx budget in the upper troposphere over the tropical South Pacific

被引:18
作者
Schultz, MG
Jacob, DJ
Bradshaw, JD
Sandholm, ST
Dibb, JE
Talbot, RW
Singh, HB
机构
[1] Univ New Hampshire, Inst Study Earth Oceans & Space, Durham, NH 03824 USA
[2] Harvard Univ, Div Engn & Appl Sci, Cambridge, MA 02139 USA
[3] Harvard Univ, Dept Earth & Planetary Sci, Cambridge, MA 02139 USA
[4] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
[5] NASA, Ames Res Ctr, Moffett Field, CA 94035 USA
关键词
D O I
10.1029/1999JD900994
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The chemical NOx budget in the upper troposphere over the tropical South Pacific is analyzed using aircraft measurements made at 6-12 km altitude in September 1995 during the Global Tropospheric Experiment (GTE) Pacific Exploratory Mission (PEM) Tropics A campaign. Chemical loss and production rates of NOx along the aircraft flight tracks are calculated with a photochemical model constrained by observations. Calculations using a standard chemical mechanism show a large missing source for NOx; chemical loss exceeds chemical production by a factor of 2.4 on average. Similar or greater NOx budget imbalances have been reported in analyses of data from previous field studies. Ammonium aerosol concentrations in PEM-Tropics A generally exceeded sulfate on a charge equivalent basis, and relative humidities were low (median 25% relative to ice). This implies that the aerosol could be dry in which case N2O5 hydrolysis would be suppressed as a sink for NOx. Suppression of N2O5 hydrolysis and adoption of new measurements of the reaction rate constants for NO2 + OH + M and HNO3 + OH reduces the median chemical imbalance in the N-x budget for PEM-Tropics A from 2.4 to 1.9. The remaining imbalance cannot be easily explained from known chemistry or long-range transport of primary NOx and may imply a major gap in our understanding of the chemical cycling of NOx in the free troposphere.
引用
收藏
页码:6669 / 6679
页数:11
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