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Exploring Oxidation in the Remote Free Troposphere: Insights From Atmospheric Tomography (ATom)

Authors :
T. P. Bui
T. B. Ryerson
Chelsea R. Thompson
Bruce C. Daube
Thomas F. Hanisco
Roisin Commane
R. A. Hannun
Hannah M. Allen
J. A. Neuman
James W. Elkins
J. M. St Clair
John D. Crounse
Colm Sweeney
Patrick R. Veres
D. O. Miller
Fred L. Moore
Michelle J. Kim
William H. Brune
Glenn M. Wolfe
Julie M. Nicely
Alex P. Teng
Jeff Peischl
Eric C. Apel
Paul O. Wennberg
A. B. Thames
Glenn S. Diskin
Kirk Ullmann
Kathryn McKain
Eric J. Hintsa
Donald R. Blake
J. P. DiGangi
Rebecca S. Hornbrook
Samuel R. Hall
Source :
Journal of Geophysical Research: Atmospheres. 125
Publication Year :
2020
Publisher :
American Geophysical Union (AGU), 2020.

Abstract

Earth's atmosphere oxidizes the greenhouse gas methane and other gases, thus determining their lifetimes and oxidation products. Much of this oxidation occurs in the remote, relatively clean free troposphere above the planetary boundary layer, where the oxidation chemistry is thought to be much simpler and better understood than it is in urban regions or forests. The NASA airborne Atmospheric Tomography study (ATom) was designed to produce cross sections of the detailed atmospheric composition in the remote atmosphere over the Pacific and Atlantic Oceans during four seasons. As part of the extensive ATom data set, measurements of the atmosphere's primary oxidant, hydroxyl (OH), and hydroperoxyl (HO₂) are compared to a photochemical box model to test the oxidation chemistry. Generally, observed and modeled median OH and HO₂ agree to with combined uncertainties at the 2σ confidence level, which is ~±40%. For some seasons, this agreement is within ~±20% below 6 km altitude. While this test finds no significant differences, OH observations increasingly exceeded modeled values at altitudes above 8 km, becoming ~35% greater, which is near the combined uncertainties. Measurement uncertainty and possible unknown measurement errors complicate tests for unknown chemistry or incorrect reaction rate coefficients that would substantially affect the OH and HO₂ abundances. Future analysis of detailed comparisons may yield additional discrepancies that are masked in the median values.

Details

ISSN :
21698996 and 2169897X
Volume :
125
Database :
OpenAIRE
Journal :
Journal of Geophysical Research: Atmospheres
Accession number :
edsair.doi...........6807e0f882f1692bd58d52e245c06059