Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour

Stratospheric water vapour influences the chemical ozone loss in the polar stratosphere via control of the polar stratospheric cloud formation. The amount of water vapour entering the stratosphere through the tropical tropopause differs substantially between simulations from chemistry–climate models...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Thölix, Laura, Karpechko, Alexey, Backman, Leif, Kivi, Rigel
Format: Text
Language:English
Published: 2019
Subjects:
Online Access:https://doi.org/10.5194/acp-18-15047-2018
https://www.atmos-chem-phys.net/18/15047/2018/
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spelling ftcopernicus:oai:publications.copernicus.org:acp67502 2023-05-15T14:50:58+02:00 Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour Thölix, Laura Karpechko, Alexey Backman, Leif Kivi, Rigel 2019-01-16 application/pdf https://doi.org/10.5194/acp-18-15047-2018 https://www.atmos-chem-phys.net/18/15047/2018/ eng eng doi:10.5194/acp-18-15047-2018 https://www.atmos-chem-phys.net/18/15047/2018/ eISSN: 1680-7324 Text 2019 ftcopernicus https://doi.org/10.5194/acp-18-15047-2018 2019-12-24T09:49:47Z Stratospheric water vapour influences the chemical ozone loss in the polar stratosphere via control of the polar stratospheric cloud formation. The amount of water vapour entering the stratosphere through the tropical tropopause differs substantially between simulations from chemistry–climate models (CCMs). This is because the present-day models, e.g. CCMs, have difficulties in capturing the whole complexity of processes that control the water transport across the tropopause. As a result there are large differences in the stratospheric water vapour between the models. In this study we investigate the sensitivity of simulated Arctic ozone loss to the simulated amount of water vapour that enters the stratosphere through the tropical tropopause. We used a chemical transport model, FinROSE-CTM, forced by ERA-Interim meteorology. The water vapour concentration in the tropical tropopause was varied between 0.5 and 1.6 times the concentration in ERA-Interim, which is similar to the range seen in chemistry–climate models. The water vapour changes in the tropical tropopause led to about 1.5 ppmv less and 2 ppmv more water vapour in the Arctic polar vortex compared to the ERA-Interim, respectively. The change induced in the water vapour concentration in the tropical tropopause region was seen as a nearly one-to-one change in the Arctic polar vortex. We found that the impact of water vapour changes on ozone loss in the Arctic polar vortex depends on the meteorological conditions. The strongest effect was in intermediately cold stratospheric winters, such as the winter of 2013/2014, when added water vapour resulted in 2 %–7 % more ozone loss due to the additional formation of polar stratospheric clouds (PSCs) and associated chlorine activation on their surface, leading to ozone loss. The effect was less pronounced in cold winters such as the 2010/2011 winter because cold conditions persisted long enough for a nearly complete chlorine activation, even in simulations with prescribed stratospheric water vapour amount corresponding to the observed values. In this case addition of water vapour to the stratosphere led to increased areas of ICE PSCs but it did not increase the chlorine activation and ozone destruction significantly. In the warm winter of 2012/2013 the impact of water vapour concentration on ozone loss was small because the ozone loss was mainly NO x -induced. The results show that the simulated water vapour concentration in the tropical tropopause has a significant impact on the Arctic ozone loss and therefore needs to be well simulated in order to improve future projections of the recovery of the ozone layer. Text Arctic Copernicus Publications: E-Journals Arctic Atmospheric Chemistry and Physics 18 20 15047 15067
institution Open Polar
collection Copernicus Publications: E-Journals
op_collection_id ftcopernicus
language English
description Stratospheric water vapour influences the chemical ozone loss in the polar stratosphere via control of the polar stratospheric cloud formation. The amount of water vapour entering the stratosphere through the tropical tropopause differs substantially between simulations from chemistry–climate models (CCMs). This is because the present-day models, e.g. CCMs, have difficulties in capturing the whole complexity of processes that control the water transport across the tropopause. As a result there are large differences in the stratospheric water vapour between the models. In this study we investigate the sensitivity of simulated Arctic ozone loss to the simulated amount of water vapour that enters the stratosphere through the tropical tropopause. We used a chemical transport model, FinROSE-CTM, forced by ERA-Interim meteorology. The water vapour concentration in the tropical tropopause was varied between 0.5 and 1.6 times the concentration in ERA-Interim, which is similar to the range seen in chemistry–climate models. The water vapour changes in the tropical tropopause led to about 1.5 ppmv less and 2 ppmv more water vapour in the Arctic polar vortex compared to the ERA-Interim, respectively. The change induced in the water vapour concentration in the tropical tropopause region was seen as a nearly one-to-one change in the Arctic polar vortex. We found that the impact of water vapour changes on ozone loss in the Arctic polar vortex depends on the meteorological conditions. The strongest effect was in intermediately cold stratospheric winters, such as the winter of 2013/2014, when added water vapour resulted in 2 %–7 % more ozone loss due to the additional formation of polar stratospheric clouds (PSCs) and associated chlorine activation on their surface, leading to ozone loss. The effect was less pronounced in cold winters such as the 2010/2011 winter because cold conditions persisted long enough for a nearly complete chlorine activation, even in simulations with prescribed stratospheric water vapour amount corresponding to the observed values. In this case addition of water vapour to the stratosphere led to increased areas of ICE PSCs but it did not increase the chlorine activation and ozone destruction significantly. In the warm winter of 2012/2013 the impact of water vapour concentration on ozone loss was small because the ozone loss was mainly NO x -induced. The results show that the simulated water vapour concentration in the tropical tropopause has a significant impact on the Arctic ozone loss and therefore needs to be well simulated in order to improve future projections of the recovery of the ozone layer.
format Text
author Thölix, Laura
Karpechko, Alexey
Backman, Leif
Kivi, Rigel
spellingShingle Thölix, Laura
Karpechko, Alexey
Backman, Leif
Kivi, Rigel
Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
author_facet Thölix, Laura
Karpechko, Alexey
Backman, Leif
Kivi, Rigel
author_sort Thölix, Laura
title Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
title_short Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
title_full Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
title_fullStr Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
title_full_unstemmed Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
title_sort linking uncertainty in simulated arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour
publishDate 2019
url https://doi.org/10.5194/acp-18-15047-2018
https://www.atmos-chem-phys.net/18/15047/2018/
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op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-18-15047-2018
https://www.atmos-chem-phys.net/18/15047/2018/
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container_title Atmospheric Chemistry and Physics
container_volume 18
container_issue 20
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