Journal
NATURE GEOSCIENCE
Volume 6, Issue 2, Pages 108-111Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/NGEO1687
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Funding
- UK NERC SOLAS (Surface Ocean Lower Atmosphere) programme
- NERC
- Natural Environment Research Council [NE/D006546/1, NE/D006538/1] Funding Source: researchfish
- NERC [NE/D006546/1, NE/D006538/1] Funding Source: UKRI
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Naturally occurring bromine-and iodine-containing compounds substantially reduce regional, and possibly even global, tropospheric ozone levels(1-4). As such, these halogen gases reduce the global warming effects of ozone in the troposphere(5), and its capacity to initiate the chemical removal of hydrocarbons such as methane. The majority of halogen-related surface ozone destruction is attributable to iodine chemistry(2). So far, organic iodine compounds have been assumed to serve as the main source of oceanic iodine emissions(1,6-9). However, known organic sources of atmospheric iodine cannot account for gas-phase iodine oxide concentrations in the lower troposphere over the tropical oceans(3,4). Here, we quantify gaseous emissions of inorganic iodine following the reaction of iodide with ozone in a series of laboratory experiments. We show that the reaction of iodide with ozone leads to the formation of both molecular iodine and hypoiodous acid. Using a kinetic box model of the sea surface layer and a one-dimensional model of the marine boundary layer, we show that the reaction of ozone with iodide on the sea surface could account for around 75% of observed iodine oxide levels over the tropical Atlantic Ocean. According to the sea surface model, hypoiodous acid-not previously considered as an oceanic source of iodine-is emitted at a rate ten-fold higher than that of molecular iodine under ambient conditions.
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