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...
Main Authors: | , , , , , , |
---|---|
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 |
Summary: | 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. |
---|---|
ISSN: | 1680-7316 1680-7324 |