THE EVOLUTION OF CLO AND NO ALONG AIR PARCEL TRAJECTORIES

被引:24
作者
SCHOEBERL, MR
DOUGLASS, AR
STOLARSKI, RS
NEWMAN, PA
LAIT, LR
TOOHEY, D
AVALLONE, L
ANDERSON, JG
BRUNE, W
FAHEY, DW
KELLY, K
机构
[1] UNIV CALIF IRVINE,DEPT GEOSCI,IRVINE,CA 92717
[2] HARVARD UNIV,ESL,ATMOSPHER RES PROJECT,CAMBRIDGE,MA 02138
[3] PENN STATE UNIV,DEPT METEOROL,UNIV PK,PA 16802
[4] NOAA,AERON LAB,BOULDER,CO 80303
关键词
D O I
10.1029/93GL01690
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Back trajectory analysis of Arctic and Antarctic aircraft data reveals that high ClO concentrations are associated with predicted polar stratospheric cloud (PSCs) encounters. The CIO concentrations within the Arctic and Antarctic polar vortices vary widely but appear to be inversely related to parcel solar exposure since the last PSC interaction. These results imply that production of NO(x) from HNO3 photolysis and reaction with OH is the mechanism for the loss of chlorine radicals through the reformation of chlorine nitrate. Highly denitrified air-parcels show no change in ClO with solar exposure. The recovery process is quantitatively duplicated using a model of chemistry along trajectories. Although PSC processing is the primary mechanism for producing elevated ClO amounts, back trajectories apparently unperturbed by PSC's also show slightly elevated ClO levels in 1992 compared to Arctic 1989 and Antarctic 1987 measurements presumably due to the presence of Pinatubo aerosol.
引用
收藏
页码:2511 / 2514
页数:4
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