Over the last five years, research led by this team has made it apparent that the reaction of iodide with ozone at the sea surface plays an important role in controlling the chemical composition of the troposphere. This process directly controls the deposition of O3 to the oceans and is the dominant source of reactive iodine to the atmosphere, which leads to significant loss of tropospheric O3. Ozone concentrations are directly impacted but through changes to the atmospheric oxidants, indirect changes also occur to methane and aerosols leading to potential ramifications on climate, air quality and food security. This is likely a biogeochemical negative feedback for tropospheric O3 and oxidants, which, since it is dependent on both atmospheric O3 and ocean iodide concentrations, will have changed over time. Iodine is also an essential human nutrient. The transport of iodine from the oceans to the atmosphere and subsequent deposition over land is a pathway by which marine iodine may enter the terrestrial food chain, and iodine radioisotopes released to the sea may be dispersed. These iodine ocean-atmosphere processes are now being incorporated into chemical transport models but critical uncertainties remain. The marine iodide distribution is poorly understood, yet it is likely that it will be subject to change as a result of changes in ocean circulation, biological productivity and ocean deoxygenation. This proposal brings together marine and atmospheric scientists in order to address uncertainties in the marine iodine flux and associated ozone sink. Specifically, it aims to quantify the dominant controls on the sea surface iodide distribution and improve parameterisation of the sea-to-air iodine flux and of ozone deposition. This will be achieved through a combination of laboratory experiments, field measurements and ocean and atmospheric modelling.