An improved estimate of inorganic iodine emissions from the ocean using a coupled surface microlayer box model
| Autor: | R. J. Pound, L. V. Brown, M. J. Evans, L. J. Carpenter |
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| Jazyk: | angličtina |
| Rok vydání: | 2024 |
| Předmět: | |
| Zdroj: | Atmospheric Chemistry and Physics, Vol 24, Pp 9899-9921 (2024) |
| Druh dokumentu: | article |
| ISSN: | 1680-7316 1680-7324 |
| DOI: | 10.5194/acp-24-9899-2024 |
| Popis: | Iodine at the ocean's surface impacts climate and health by removing ozone (O3) from the troposphere both directly via ozone deposition to seawater and indirectly via the formation of iodine gases that are released into the atmosphere. Here we present a new box model of the ocean surface microlayer that couples oceanic O3 dry deposition to inorganic chemistry to predict inorganic iodine emissions. This model builds on the previous work of Carpenter et al. (2013), improving both chemical and physical processes. This new box model predicts iodide depletion in the top few micrometres of the ocean surface due to rapid chemical loss to ozone competing with replenishment from underlying water. From this box model, we produce parameterized equations for HOI and I2 emissions, which are implemented into the global chemical transport model GEOS-Chem along with an updated sea surface iodide climatology. Compared to the previous model, inorganic iodine emissions from some tropical waters decrease by as much as half, while higher-latitude emissions increase by a factor of ≫10. With these large local changes, global total inorganic iodine emissions increased by ∼49 % (2.99 to 4.48 Tg) compared to the previous parameterization. This results in a negligible change in average tropospheric OH ( %) and tropospheric methane lifetime ( %). The annual mean tropospheric O3 burden decreases (−1.5 % to 325 Tg); however, higher-latitude surface O3 concentrations decrease by as much as 20 %. |
| Databáze: | Directory of Open Access Journals |
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