The influence of deep convection on HCHO and HO in the upper troposphere over Europe

Deep convection is an efficient mechanism for vertical trace gas transport from Earth's surface to the upper troposphere (UT). The convective redistribution of short-lived trace gases emitted at the surface typically results in a C-shaped profile. This redistribution mechanism can impact ph...

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Main Authors: H. Bozem, A. Pozzer, H. Harder, M. Martinez, J. Williams, J. Lelieveld, H. Fischer
Format: Article
Language:English
Published: Copernicus Publications 2017-10-01
Series:Atmospheric Chemistry and Physics
Online Access:https://www.atmos-chem-phys.net/17/11835/2017/acp-17-11835-2017.pdf
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spelling doaj-652c6193134d427fa0206e6ac34749f52020-11-25T00:32:40ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242017-10-0117118351184810.5194/acp-17-11835-2017The influence of deep convection on HCHO and HO in the upper troposphere over EuropeH. Bozem0H. Bozem1A. Pozzer2H. Harder3M. Martinez4J. Williams5J. Lelieveld6H. Fischer7Atmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, Germanynow at: Institute for Atmospheric Physics, Johannes Gutenberg University, Mainz, GermanyAtmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, GermanyAtmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, GermanyAtmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, GermanyAtmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, GermanyAtmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, GermanyAtmospheric Chemistry Department, Max Planck Institute for Chemistry, P.O. Box 3060, 55020 Mainz, GermanyDeep convection is an efficient mechanism for vertical trace gas transport from Earth's surface to the upper troposphere (UT). The convective redistribution of short-lived trace gases emitted at the surface typically results in a C-shaped profile. This redistribution mechanism can impact photochemical processes, e.g. ozone and radical production in the UT on a large scale due to the generally longer lifetimes of species like formaldehyde (HCHO) and hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), which are important HO<sub><i>x</i></sub> precursors (HO<sub><i>x</i></sub> =  OH + HO<sub>2</sub> radicals). Due to the solubility of HCHO and H<sub>2</sub>O<sub>2</sub> their transport may be suppressed as they are efficiently removed by wet deposition. Here we present a case study of deep convection over Germany in the summer of 2007 within the framework of the HOOVER II project. Airborne in situ measurements within the in- and outflow regions of an isolated thunderstorm provide a unique data set to study the influence of deep convection on the transport efficiency of soluble and insoluble trace gases. Comparing the in- and outflow indicates an almost undiluted transport of insoluble trace gases from the boundary layer to the UT. The ratios of out : inflow of CO and CH<sub>4</sub> are 0.94 ± 0.04 and 0.99 ± 0.01, respectively. For the soluble species HCHO and H<sub>2</sub>O<sub>2</sub> these ratios are 0.55 ± 0.09 and 0.61 ± 0.08, respectively, indicating partial scavenging and washout. Chemical box model simulations show that post-convection secondary formation of HCHO and H<sub>2</sub>O<sub>2</sub> cannot explain their enhancement in the UT. A plausible explanation, in particular for the enhancement of the highly soluble H<sub>2</sub>O<sub>2</sub>, is degassing from cloud droplets during freezing, which reduces the retention coefficient.https://www.atmos-chem-phys.net/17/11835/2017/acp-17-11835-2017.pdf
collection DOAJ
language English
format Article
sources DOAJ
author H. Bozem
H. Bozem
A. Pozzer
H. Harder
M. Martinez
J. Williams
J. Lelieveld
H. Fischer
spellingShingle H. Bozem
H. Bozem
A. Pozzer
H. Harder
M. Martinez
J. Williams
J. Lelieveld
H. Fischer
The influence of deep convection on HCHO and HO in the upper troposphere over Europe
Atmospheric Chemistry and Physics
author_facet H. Bozem
H. Bozem
A. Pozzer
H. Harder
M. Martinez
J. Williams
J. Lelieveld
H. Fischer
author_sort H. Bozem
title The influence of deep convection on HCHO and HO in the upper troposphere over Europe
title_short The influence of deep convection on HCHO and HO in the upper troposphere over Europe
title_full The influence of deep convection on HCHO and HO in the upper troposphere over Europe
title_fullStr The influence of deep convection on HCHO and HO in the upper troposphere over Europe
title_full_unstemmed The influence of deep convection on HCHO and HO in the upper troposphere over Europe
title_sort influence of deep convection on hcho and ho in the upper troposphere over europe
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2017-10-01
description Deep convection is an efficient mechanism for vertical trace gas transport from Earth's surface to the upper troposphere (UT). The convective redistribution of short-lived trace gases emitted at the surface typically results in a C-shaped profile. This redistribution mechanism can impact photochemical processes, e.g. ozone and radical production in the UT on a large scale due to the generally longer lifetimes of species like formaldehyde (HCHO) and hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), which are important HO<sub><i>x</i></sub> precursors (HO<sub><i>x</i></sub> =  OH + HO<sub>2</sub> radicals). Due to the solubility of HCHO and H<sub>2</sub>O<sub>2</sub> their transport may be suppressed as they are efficiently removed by wet deposition. Here we present a case study of deep convection over Germany in the summer of 2007 within the framework of the HOOVER II project. Airborne in situ measurements within the in- and outflow regions of an isolated thunderstorm provide a unique data set to study the influence of deep convection on the transport efficiency of soluble and insoluble trace gases. Comparing the in- and outflow indicates an almost undiluted transport of insoluble trace gases from the boundary layer to the UT. The ratios of out : inflow of CO and CH<sub>4</sub> are 0.94 ± 0.04 and 0.99 ± 0.01, respectively. For the soluble species HCHO and H<sub>2</sub>O<sub>2</sub> these ratios are 0.55 ± 0.09 and 0.61 ± 0.08, respectively, indicating partial scavenging and washout. Chemical box model simulations show that post-convection secondary formation of HCHO and H<sub>2</sub>O<sub>2</sub> cannot explain their enhancement in the UT. A plausible explanation, in particular for the enhancement of the highly soluble H<sub>2</sub>O<sub>2</sub>, is degassing from cloud droplets during freezing, which reduces the retention coefficient.
url https://www.atmos-chem-phys.net/17/11835/2017/acp-17-11835-2017.pdf
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