Reactivity of Inorganic Mn and Mn Desferrioxamine B with O2, O2–, and H2O2 in Seawater

Wuttig, K, Heller, MI and Croot, PL 2013 Reactivity of Inorganic Mn and Mn Desferrioxamine B with O2, O2–, and H2O2 in Seawater. Environmental Science & Technology. 10257-10265. https://doi.org/10.1021/es4016603

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Official URL: http://dx.doi.org/10.1021/es4016603

Abstract/Summary

Manganese (Mn) is a required element for oceanic phytoplankton as it plays a critical role in photosynthesis, through its unique redox chemistry, as the active site in photosystem II, and in enzymes that act as defenses against reactive oxygen species (ROS), most notably for protection against superoxide (O2?), through the action of superoxide dismutase (SOD), and against hydrogen peroxide (H2O2) via peroxidases and catalases. The distribution and redox speciation of Mn in the ocean is also apparently controlled by reactions with ROS. Here we examine the connections between ROS and dissolved Mn species in the upper ocean using field and laboratory experimental data. Our results suggest it is unlikely that significant concentrations of Mn(III) are produced in the euphotic zone, as in the absence of evidence for the existence of strong Mn(III) ligands, Mn(II) reacts with O2? to form the short-lived transient manganous superoxide, MnO2+, which may react rapidly with other redox species in a manner similar to O2?. Experiments with the strong Mn(III) chelator, desferrioxamine B (DFB), in seawater indicated that the Mn(III) species are unlikely to form, as formation of the precursor Mn(II) complex is hindered due to the stability of the Ca complex with DFB.

Item Type: Publication - Article
Subjects: Chemistry
Ecology and Environment
Marine Sciences
Divisions: Plymouth Marine Laboratory > Science Areas > Cycling in the Sunlit Ocean (expired)
Depositing User: Mrs Julia Crocker
Date made live: 03 Mar 2014 11:47
Last Modified: 05 Nov 2018 12:30
URI: https://plymsea.ac.uk/id/eprint/5587

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