1Deutsches Zentrum für Luft- und Raumfahrt, Institut für Physik der Atmosphäre, Oberpfaffenhofen, Germany
2Johannes-Gutenberg-Universität, Institut für Physik der Atmosphäre, Mainz, Germany
Received: 28 Jun 2012 – Published in Atmos. Chem. Phys. Discuss.: 17 Sep 2012
Abstract. The impact of a recently proposed HNO3-forming channel of the HO2 + NO reaction on atmospheric ozone, methane and their precursors is assessed with the aim to investigate its effects on aviation NOx induced radiative forcing.
Revised: 17 Jan 2013 – Accepted: 25 Feb 2013 – Published: 15 Mar 2013
The first part of the study addresses the differences in stratospheric and tropospheric HOx-NOx chemistry in general, by comparing a global climate simulation without the above reaction to two simulations with different rate coefficient parameterizations for HO2 + NO → HNO3. A possible enhancement of the reaction by humidity, as found by a laboratory study, particularly reduces the oxidation capacity of the atmosphere, increasing methane lifetime significantly. Since methane lifetime is an important parameter for determining global methane budgets, this might affect estimates of the anthropogenic greenhouse effect.
In the second part aviation NOx effects are isolated independently for each of the three above simulations. Warming and cooling effects of aircraft NOx emissions are both enhanced when considering the HNO3-forming channel, but the sum is shifted towards negative radiative forcing. Uncertainties associated with the inclusion of the HO2 + NO → HNO3 reaction and with its corresponding rate coefficient propagate a considerable additional uncertainty on estimates of the climate impact of aviation and on NOx-related mitigation strategies.
Citation: Gottschaldt, K., Voigt, C., Jöckel, P., Righi, M., Deckert, R., and Dietmüller, S.: Global sensitivity of aviation NOx effects to the HNO3-forming channel of the HO2 + NO reaction, Atmos. Chem. Phys., 13, 3003-3025, doi:10.5194/acp-13-3003-2013, 2013.