Temporal behavior of manganese and iron in a sandy coastal sediment exposed to water column anoxia |
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| Authors: | Email author" target="_blank">Erik?KristensenEmail author Kim?Dyrberg?Kristiansen Mikael?Hjorth?Jensen |
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| Institution: | 1.Institute of Biology,Odense University, SDU,Odense M,Denmark;2.Nature Management and Water Quality Division,County of Fyn,Odense S?,Denmark |
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| Abstract: | The influence of bottom water anoxia on manganese (Mn), iron (Fe), and sulfur (S) biogeochemistry was examined in defaunated sandy sediment from Kærby Fed, Denmark, under controlled laboratory incubations. The initial narrow peaks and steep gradients in solid Mn(IV) and Fe(III) as well as porewater Mn2+ and Fe2+ observed in the upper 2–5 cm of the sediment indicate rapid metal reduction-oxidation cycles under oxic conditions in the overlying water. The fe zones were generally displaced about 0.5 cm downward compared with the Mn zones due to differences in reactivity. Mn(IV) was reduced and gradually disappeared first (within 10 d) when the sediment was exposed to anoxia followed by reduction and disappearance of Fe(III) (day 7 to 18). The associated loss of Mn2+ to the overlying water was most rapid during the first 15 d, whereas the Fe2+ efflux initiated around day 10, and after a few days with modest rates the efflux peaked around day 20. A considerable portion of the total Mn (26%) and Fe (23%) inventory initially present in the sediment was lost by efflux after about 1 mo of anoxia. The ability of the sediment to retain upward diffusion of H2S gradually disappeared in a temporal pattern closely related to the changes in pool size of the reactive Mn and Fe present. The total metal pool in Kærby Fed sediment prevented H2S release to the overlying water for at least a month of anoxia. It is speculated that external supplies from the overlying water allows a rapid refuelling of surface Mn and Fe oxides in the field when oxic conditions returns between periods of anoxia. |
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