Are there interactions of iodine and sulfur species in marine air photochemistry?
- 20 December 1990
- journal article
- Published by American Geophysical Union (AGU) in Journal of Geophysical Research: Atmospheres
- Vol. 95 (D13) , 22319-22341
- https://doi.org/10.1029/jd095id13p22319
Abstract
Portions of the global cycles of sulfur and iodine could be intertwined in reactions resulting from the emissions of dimethyl sulfide (DMS) and methyl iodide. A two‐dimensional photochemical model of a marine tropical tropospheric synoptic system is used to analyze the consequences of these emissions through their atmospheric transformation cycles to aerosols. Following one line of analysis, the reaction of IO+DMS → DMSO+I could play a significant role, ∼30–50%, in destroying DMS, if the reaction proceeds at the published fast rate. Under these assumptions, the concentrations of DMSO (dimethyl sulfoxide), dimethyl sulfone (DMSO2), and sulfate appear to set rather strict upper limits on the extent of the reaction over the global oceans, and hence, on [IO], which is < 2×105 molecule cm−3. DMS plays an important role in the iodine cycle by converting IO into I. The formation of a reservoir species HOI, following H abstraction by IO, may help explain the high concentrations and apparent strong diurnal variation of filter‐sampled inorganic iodine gases and help to explain low [IO] values. In an alternate, preferred, line of analysis, the rate of reaction of IO+DMS may be much slower, < 10−12 cm3 molecule−1s−1 and the I and S cycles remain decoupled: in this case, it appears that the OH+DMS addition reaction could proceed ∼30% to form DMSO. The mean concentration and variations of gaseous and particulate iodine species are also better simulated. A simple aerosol model describing fine and coarse particles is used to close the S budget, and, if only a minor role is played by DMSO, the budget compares well with data. Simulated SO2 concentrations for the upper troposphere are highly dependent on upper tropospheric [OH]. The paper concentrates on remote tropical ocean regions and includes simulations of the spatial and diurnal variation of iodine species I, IO, HI, HOI, IONO2, I2O2 and Itot(particulate) the sulfur species DMS, DMSO, DMSO2, MSA (methane sulfonic acid), SO2, and SO4=(particulate), as well as the species OH, HO2, and H2O2.This publication has 86 references indexed in Scilit:
- Nucleation of sulfuric acid-water and methanesulfonic acid-water solution particles: Implications for the atmospheric chemistry of organosulfur speciesAtmospheric Environment (1967), 1988
- Nucleation in the MSA-water vapor systemAtmospheric Environment (1967), 1987
- Measurements of the aerosol concentrations of methanesulphonic acid, dimethyl sulphoxide and dimethyl sulphone in the marine atmosphere of the British IslesAtmospheric Environment (1967), 1987
- Atmospheric methanesulfonic acid and non‐sea‐salt sulfate at Fanning and American SamoaGeophysical Research Letters, 1985
- The hydrolysis of iodine: Equilibria at high temperaturesJournal of Nuclear Materials, 1985
- Oxidation rates of SO2 in sea-water and sea-salt aerosolsAtmospheric Environment (1967), 1984
- Halogens in the atmosphereReviews of Geophysics, 1981
- Rate of reaction of OH with COSGeophysical Research Letters, 1980
- New particle formation in the presence of an aerosolAtmospheric Environment (1967), 1979
- Cumulus Convection and Larger Scale Circulations I. Broadscale and Mesoscale ConsiderationsMonthly Weather Review, 1973