High dimethylsulfide photolysis rates in nitrate-rich Antarctic waters

Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 31 (2004): L11307, doi:10.1029/2004GL019863. The photochemistry o...

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Bibliographic Details
Published in:Geophysical Research Letters
Main Authors: Toole, Dierdre A., Kieber, David J., Kiene, Ronald P., White, E. M., Bisgrove, J., del Valle, Daniela A., Slezak, D.
Format: Article in Journal/Newspaper
Language:English
Published: American Geophysical Union 2004
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Online Access:https://hdl.handle.net/1912/3309
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Summary:Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 31 (2004): L11307, doi:10.1029/2004GL019863. The photochemistry of dimethylsulfide (DMS) was examined in the Southern Ocean to assess its impact on the biogeochemical dynamics of DMS in Antarctic waters. Very high DMS photolysis rate constants (0.16–0.23 h−1) were observed in surface waters exposed to full sunlight. DMS photolysis rates increased linearly with added nitrate concentrations, and 35% of the DMS loss in unamended samples was attributed to the photochemistry of ambient nitrate (29 μM). Experiments with optical filters showed that the UV-A band of sunlight (320–400 nm) accounted for ~65% of DMS photolysis suggesting that dissolved organic matter was the main photosensitizer for DMS photolysis. During the austral spring, DMS photolysis was the dominant loss mechanism under non-bloom and non-ice cover conditions owing to the high doses and deep penetration of UV radiation in the water column, low observed microbial consumption rates, and high in situ nitrate concentrations. This work was supported by NSF (OPP- 0230499, DJK; OPP-0230497, RPK).