Atmospheric CH₄, CO and OH from 1860 to 1985
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Thompson, Anne M., and Ralph J. Cicerone. “Atmospheric CH₄, CO and OH from 1860 to 1985.” Nature 321, no. 6066 (May 1986): 148–50. https://doi.org/10.1038/321148a0.
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This work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
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Abstract
Atmospheric methane, CO and the gaseous OH radical are interdependent: if CH₄, CO or OH is perturbed, background concentrations of the other two constituents are affected. Perturbations to OH alter photo-oxidation rates of numerous natural and anthropogenic trace gases and affect lifetimes of those species that pass from the Earth's surface to the free troposphere and stratosphere. It is now known that global atmospheric methane concentrations are increasing¹⁻⁶; less definite data suggest that carbon monoxide is also increasing¹,⁷⁻⁹. Even before the measurements of refs 1–9 were made, modelling studies of CH₄-CO-OH coupling had led to predictions¹⁰⁻¹² of future temporal increases of CH₄ and CO. Here we look backwards in time, using a photochemical model to simulate the trace-gas composition of the unpolluted troposphere at the start of the industrial era (taken as 1860), and at intervals up to 1985. We find that the OH concentration in the background troposphere has decreased significantly and O₃ has increased due to increases of CH₄ and CO; calculated changes depend on temporal trends of NOₓ (NOₓ = NO + NO₂), for which no historical data are available. The calculations allow recent trace-gas trends affecting background chemistry and climate to be viewed in a longer-term context.