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Originally published in Science Express on 3 May 2001
Science 8 June 2001: Vol. 292. no. 5523, pp. 1882 - 1888
DOI: 10.1126/science.1058673
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Research Articles
Evidence for Substantial Variations of Atmospheric Hydroxyl Radicals in the Past Two Decades
R. G. Prinn,1
J. Huang,1
R. F. Weiss,2
D. M. Cunnold,3
P. J. Fraser,4
P. G. Simmonds,5
A. McCulloch,5
C. Harth,2
P. Salameh,2
S. O'Doherty,5
R. H. J. Wang,3
L. Porter,6
B. R. Miller2
The hydroxyl radical (OH) is the dominant oxidizing
chemical in the atmosphere. It destroys most air pollutants and many
gases involved in ozone depletion and the greenhouse effect. Global measurements of 1,1,1-trichloroethane (CH3CCl3,
methyl chloroform) provide an accurate method for determining the
global and hemispheric behavior of OH. Measurements show that
CH3CCl3 levels rose steadily from 1978 to reach
a maximum in 1992 and then decreased rapidly to levels in 2000 that
were lower than the levels when measurements began in 1978. Analysis of
these observations shows that global OH levels were growing between
1978 and 1988, but the growth rate was decreasing at a rate of
0.23 ± 0.18% year 2, so that OH levels began declining
after 1988. Overall, the global average OH trend between 1978 and 2000 was 0.64 ± 0.60% year 1. These variations imply
important and unexpected gaps in current understanding of the
capability of the atmosphere to cleanse itself.
1 Department of Earth, Atmospheric, and
Planetary Sciences, Massachusetts Institute of Technology, Cambridge,
MA 02139, USA.
2 Scripps Institution of
Oceanography, University of California, San Diego, La Jolla, CA 92093, USA.
3 Department of Earth and Atmospheric Sciences,
Georgia Institute of Technology, Atlanta, GA 30332, USA.
4 Atmospheric Research, Commonwealth Scientific and
Industrial Research Organization, Aspendale, Victoria 3195, Australia.
5 School of Chemistry, University of
Bristol, Bristol 8S8 1TH, UK.
6 Cape Grim Baseline
Air Pollution Station, Bureau of Meteorology, Smithton, Tasmania 7330, Australia.
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