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Discussion papers
https://doi.org/10.5194/acp-2019-1043
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-2019-1043
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.

Submitted as: research article 20 Nov 2019

Submitted as: research article | 20 Nov 2019

Review status
This discussion paper is a preprint. It is a manuscript under review for the journal Atmospheric Chemistry and Physics (ACP).

Influences of oceanic ozone deposition on tropospheric photochemistry

Ryan J. Pound1, Tomás Sherwen1,2, Detlev Helmig3, Lucy J. Carpenter1, and Mat J. Evans1,2 Ryan J. Pound et al.
  • 1Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, York, YO10 5DD, UK
  • 2National Centre for Atmospheric Science, University of York, York, YO10 5DD, UK
  • 3Institute of Alpine and Arctic Research, University of Colorado at Boulder, Boulder, Colorado, USA

Abstract. The deposition of ozone to seawater is an important ozone sink. Despite constituting as much as a third of the total ozone deposition, it receives significantly less attention than the deposition to terrestrial ecosystems. Models have typically calculated the deposition rate based on a resistance-in-series model with a uniform waterside resistance. This leads to models having an essentially uniform deposition velocity of approximately 0.05 cm s−1 to seawater, which is significantly higher than the limited observational dataset. Following from Luhar et al. (2018) we include a representation of the oceanic deposition of ozone into the GEOS-Chem model of atmospheric chemistry and transport based on its reaction with sea-surface iodide. The updated scheme halves the calculated annual area-weighted mean deposition velocity to water from 0.0464 cm s−1 (25th and 75th percentiles of 0.0461 cm s−1 and 0.0471 cm s−1 respectively), to 0.0231 cm s−1 (25th and 75th percentiles of 0.0121 cm s−1 and 0.0303 cm s−1 respectively). The calculated ozone deposition velocity varies from 0.009 cm s−1 in polar waters to 0.040 cm s−1 at the tropics. This improves comparisons to observations. The variability is driven mainly by the temperature dependant rate constant for the reaction between iodide and ozone, the temperature dependence of the solubility and variations in the ocean iodide concentration. The calculated annual deposition flux of ozone to the ocean is reduced from 222 Tg yr−1 to 112 Tg yr−1, and overall deposition of ozone to all surface types reduces from 862 Tg yr−1 to 758 Tg yr−1. Tropospheric ozone burdens and global mean OH increase from 324 Tg to 328 Tg, and from 1.17 × 106 molec cm−3 to 1.18 × 106 molec cm−3, respectively. 34 % of surface grid boxes experience a 10 % or greater increase in ozone concentration. Comparisons between observations of surface ozone and the model are improved with the new parameterization notably around the Southern Ocean. Process level representation of oceanic deposition of ozone thus appears essential for representing the concentration of surface ozone over the planet.

Ryan J. Pound et al.
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Ryan J. Pound et al.
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Short summary
Ozone is an important pollutant with impacts on health and the environment. Ozone is lost to plants, land and the oceans. Loss to the ocean is slow compared to all other types of land cover and hasn’t received as much attention. We build on previous work to more accurately model ozone loss to the ocean. We find changes in the concentration of ozone over the oceans, notably the Southern Ocean which improves model performance.
Ozone is an important pollutant with impacts on health and the environment. Ozone is lost to...
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