Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry
A transient model simulation of the 40-year time period 1960 to 1999 with the coupled climate-chemistry model (CCM) ECHAM4.L39(DLR)/CHEMshows a stratospheric water vapor increase over the last two decades of 0.7ppmv and, additionally, a short-term increase after major volcanic eruptions. Furthermore...
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Format: | Article in Journal/Newspaper |
Language: | English |
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Copernicus Publications
2005
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Online Access: | https://doaj.org/article/2172b8ed28d347eabc3c0882397caafd |
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author | A. Stenke V. Grewe |
author_facet | A. Stenke V. Grewe |
author_sort | A. Stenke |
collection | Directory of Open Access Journals: DOAJ Articles |
description | A transient model simulation of the 40-year time period 1960 to 1999 with the coupled climate-chemistry model (CCM) ECHAM4.L39(DLR)/CHEMshows a stratospheric water vapor increase over the last two decades of 0.7ppmv and, additionally, a short-term increase after major volcanic eruptions. Furthermore, a long-term decrease in global total ozone as well as a short-term ozone decline in the tropics after volcanic eruptions are modeled. In order to understand the resulting effects of the water vapor changes on lower stratospheric ozone chemistry, different perturbation simulations were performed with the CCM ECHAM4.L39(DLR)/CHEMfeeding the water vapor perturbations only to the chemistry part. Two different long-term perturbations of lower stratospheric water vapor, +1ppmv and +5ppmv, and a short-term perturbation of +2ppmv with an e-folding time of two months were applied. An additional stratospheric water vapor amount of 1ppmv results in a 5–10% OHincrease in the tropical lower stratosphere between 100 and 30hPa. As a direct consequence of the OHincrease the ozone destruction by the HO x cycle becomes 6.4% more effective. Coupling processes between the HO x -family and the NO x /ClO x -family also affect the ozone destruction by other catalytic reaction cycles. The NO x cycle becomes 1.6% less effective, whereas the effectiveness of the ClO x cycle is again slightly enhanced. A long-term water vapor increase does not only affect gas-phase chemistry, but also heterogeneous ozone chemistry in polar regions. The model results indicate an enhanced heterogeneous ozone depletion during antarctic spring due to a longer PSC existence period. In contrast, PSC formation in the northern hemisphere polar vortex and therefore heterogeneous ozone depletion during arctic spring are not affected by the water vapor increase, because of the less PSC activity. Finally, this study shows that 10% of the global total ozone decline in the transient model run can be explained by the modeled water vapor increase, but the simulated tropical ... |
format | Article in Journal/Newspaper |
genre | Antarc* Antarctic Arctic |
genre_facet | Antarc* Antarctic Arctic |
geographic | Antarctic Arctic |
geographic_facet | Antarctic Arctic |
id | ftdoajarticles:oai:doaj.org/article:2172b8ed28d347eabc3c0882397caafd |
institution | Open Polar |
language | English |
op_collection_id | ftdoajarticles |
op_relation | http://www.atmos-chem-phys.net/5/1257/2005/acp-5-1257-2005.pdf https://doaj.org/toc/1680-7316 https://doaj.org/toc/1680-7324 1680-7316 1680-7324 https://doaj.org/article/2172b8ed28d347eabc3c0882397caafd |
op_source | Atmospheric Chemistry and Physics, Vol 5, Iss 5, Pp 1257-1272 (2005) |
publishDate | 2005 |
publisher | Copernicus Publications |
record_format | openpolar |
spelling | ftdoajarticles:oai:doaj.org/article:2172b8ed28d347eabc3c0882397caafd 2025-01-16T19:08:03+00:00 Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry A. Stenke V. Grewe 2005-01-01T00:00:00Z https://doaj.org/article/2172b8ed28d347eabc3c0882397caafd EN eng Copernicus Publications http://www.atmos-chem-phys.net/5/1257/2005/acp-5-1257-2005.pdf https://doaj.org/toc/1680-7316 https://doaj.org/toc/1680-7324 1680-7316 1680-7324 https://doaj.org/article/2172b8ed28d347eabc3c0882397caafd Atmospheric Chemistry and Physics, Vol 5, Iss 5, Pp 1257-1272 (2005) Physics QC1-999 Chemistry QD1-999 article 2005 ftdoajarticles 2022-12-31T01:01:18Z A transient model simulation of the 40-year time period 1960 to 1999 with the coupled climate-chemistry model (CCM) ECHAM4.L39(DLR)/CHEMshows a stratospheric water vapor increase over the last two decades of 0.7ppmv and, additionally, a short-term increase after major volcanic eruptions. Furthermore, a long-term decrease in global total ozone as well as a short-term ozone decline in the tropics after volcanic eruptions are modeled. In order to understand the resulting effects of the water vapor changes on lower stratospheric ozone chemistry, different perturbation simulations were performed with the CCM ECHAM4.L39(DLR)/CHEMfeeding the water vapor perturbations only to the chemistry part. Two different long-term perturbations of lower stratospheric water vapor, +1ppmv and +5ppmv, and a short-term perturbation of +2ppmv with an e-folding time of two months were applied. An additional stratospheric water vapor amount of 1ppmv results in a 5–10% OHincrease in the tropical lower stratosphere between 100 and 30hPa. As a direct consequence of the OHincrease the ozone destruction by the HO x cycle becomes 6.4% more effective. Coupling processes between the HO x -family and the NO x /ClO x -family also affect the ozone destruction by other catalytic reaction cycles. The NO x cycle becomes 1.6% less effective, whereas the effectiveness of the ClO x cycle is again slightly enhanced. A long-term water vapor increase does not only affect gas-phase chemistry, but also heterogeneous ozone chemistry in polar regions. The model results indicate an enhanced heterogeneous ozone depletion during antarctic spring due to a longer PSC existence period. In contrast, PSC formation in the northern hemisphere polar vortex and therefore heterogeneous ozone depletion during arctic spring are not affected by the water vapor increase, because of the less PSC activity. Finally, this study shows that 10% of the global total ozone decline in the transient model run can be explained by the modeled water vapor increase, but the simulated tropical ... Article in Journal/Newspaper Antarc* Antarctic Arctic Directory of Open Access Journals: DOAJ Articles Antarctic Arctic |
spellingShingle | Physics QC1-999 Chemistry QD1-999 A. Stenke V. Grewe Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
title | Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
title_full | Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
title_fullStr | Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
title_full_unstemmed | Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
title_short | Simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
title_sort | simulation of stratospheric water vapor trends: impact on stratospheric ozone chemistry |
topic | Physics QC1-999 Chemistry QD1-999 |
topic_facet | Physics QC1-999 Chemistry QD1-999 |
url | https://doaj.org/article/2172b8ed28d347eabc3c0882397caafd |