4.7 Article

Iodine chemistry in the chemistry-climate model SOCOL-AERv2-I

Journal

GEOSCIENTIFIC MODEL DEVELOPMENT
Volume 14, Issue 10, Pages 6623-6645

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/gmd-14-6623-2021

Keywords

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Funding

  1. Schweizerischer Nationalfonds zur Forderung der Wissenschaftlichen Forschung [200020_182239]
  2. US National Science Foundation [AGS-2027252, AGS-1261740, AGS-1104104]
  3. Ministry of Science and Higher Education of the Russian Federation [075-15-2021-583]

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This paper introduces a new version of the chemistry-climate model SOCOL-AERv2 with an added iodine chemistry module. The study shows that iodine has a significant impact on ozone, particularly in the lower stratosphere, resulting in reduced ozone concentrations. Sensitivity tests reveal that doubling iodine emissions globally leads to an additional decrease in the ozone column.
In this paper, we present a new version of the chemistry-climate model SOCOL-AERv2 supplemented by an iodine chemistry module. We perform three 20-year ensemble experiments to assess the validity of the modeled iodine and to quantify the effects of iodine on ozone. The iodine distributions obtained with SOCOL-AERv2-I agree well with AMAX-DOAS observations and with CAM-chem model simulations. For the present-day atmosphere, the model suggests that the iodine-induced chemistry leads to a 3 %-4 % reduction in the ozone column, which is greatest at high latitudes. The model indicates the strongest influence of iodine in the lower stratosphere with 30 ppbv less ozone at low latitudes and up to 100 ppbv less at high latitudes. In the troposphere, the account of the iodine chemistry reduces the tropospheric ozone concentration by 5 %-10 % depending on geographical location. In the lower troposphere, 75 % of the modeled ozone reduction originates from inorganic sources of iodine, 25 % from organic sources of iodine. At 50 hPa, the results show that the impacts of iodine from both sources are comparable. Finally, we determine the sensitivity of ozone to iodine by applying a 2-fold increase in iodine emissions, as it might be representative for iodine by the end of this century. This reduces the ozone column globally by an additional 1.5 %-2.5 %. Our results demonstrate the sensitivity of atmospheric ozone to iodine chemistry for present and future conditions, but uncertainties remain high due to the paucity of observational data of iodine species.

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