On the possibility of iodide oxidation in the near-surface of the Black Sea and its implications to iodine in the general ocean

Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this co...

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Published inDeep-sea research. Part I, Oceanographic research papers Vol. 48; no. 11; pp. 2397 - 2412
Main Authors Truesdale, Victor W, Watts, Simon F, Rendell, A.R
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.11.2001
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Pergamon Press Inc
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Abstract Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 μM) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89×10 −4 mol I m −2 a −1. The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO 3 −/I − and I 2/I − couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate–sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.
AbstractList Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 mu M) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89 x 10 super(-4) mol Im super(-2)a super(-1). The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO super(-) sub(3)/I super(-) and I sub(2)/I super(-) couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate-sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.
Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 μM) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89×10 −4 mol I m −2 a −1. The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO 3 −/I − and I 2/I − couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate–sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.
Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem.
Author Watts, Simon F
Truesdale, Victor W
Rendell, A.R
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Issue 11
Keywords Iodate
Iodide
Entrainment model
Redox modelling
Sulfur
Black Sea
advection
sea water
models
oxidation
halides
iodides
surface water
hydrochemistry
Asia
iodates
sulfur
iodine
Mediterranean Sea
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Snippet Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of...
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SubjectTerms Bacteria
Black Sea
Earth sciences
Earth, ocean, space
Entrainment model
Exact sciences and technology
External geophysics
Geochemistry
Iodate
Iodide
Marine
Mineralogy
Oceanography
Oxidation
Physical and chemical properties of sea water
Physics of the oceans
Redox modelling
Silicates
Sulfur
Water geochemistry
Title On the possibility of iodide oxidation in the near-surface of the Black Sea and its implications to iodine in the general ocean
URI https://dx.doi.org/10.1016/S0967-0637(01)00021-8
https://www.proquest.com/docview/196702613/abstract/
https://search.proquest.com/docview/18180207
Volume 48
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