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dc.contributor.authorMoore, RMen_US
dc.contributor.authorGroszko, W.en_US
dc.date.accessioned2013-06-19T18:02:26Z
dc.date.available2013-06-19T18:02:26Z
dc.date.issued1999-05en_US
dc.identifier.citationMoore, RM, and W. Groszko. 1999. "Methyl iodide distribution in the ocean and fluxes to the atmosphere." Journal of Geophysical Research-Oceans 104(C5): 11163-11171. DOI:10.1029/1998JC900073en_US
dc.identifier.issn0148-0227en_US
dc.identifier.urihttp://dx.doi.org/10.1029/1998JC900073en_US
dc.identifier.urihttp://hdl.handle.net/10222/27125
dc.description.abstractMethyl iodide concentrations have been measured in air samples, surface, and subsurface waters of the NW Atlantic, NE Atlantic, and Pacific Oceans. They are shown to be substantially oversaturated in all surface waters. Our best estimate of methyl iodide flux from the ocean to the atmosphere is 0.9 - 2.5 x 10(9) mol yr(-1), but further substantial and unquantifiable uncertainities exist because of the limited spatial and temporal data on which this flux estimate is based. Pronounced subsurface maxima in methyl iodide concentrations seen in the Pacific Ocean and the Sargasso Sea are thought to result from production and accumulation of the gas in the relatively poorly ventilated waters beneath the surface mixed layer. Our calculations suggest that latitudinal variations in methyl iodide concentrations in the Pacific Ocean are partly controlled by temperature-dependent chemical loss.en_US
dc.relation.ispartofJournal of Geophysical Research-Oceansen_US
dc.titleMethyl iodide distribution in the ocean and fluxes to the atmosphereen_US
dc.typearticleen_US
dc.identifier.volume104en_US
dc.identifier.issue5en_US
dc.identifier.startpage11163en_US
dc.rights.holderThis paper was published by AGU. Copyright 1999 American Geophysical Union
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