De. Canfield et al., THE ANAEROBIC DEGRADATION OF ORGANIC-MATTER IN DANISH COASTAL SEDIMENTS - IRON REDUCTION, MANGANESE REDUCTION, AND SULFATE REDUCTION, Geochimica et cosmochimica acta, 57(16), 1993, pp. 3867-3883
We used a combination of porewater and solid phase analysis as well as
a series of sediment incubations, to quantify organic carbon oxidatio
n by dissimilatory Fe reduction, Mn reduction, and sulfate reduction,
in sediments from the Skagerrak (located off the northeast coast of Ju
tland, Denmark). In the deep portion of the basin, surface Mn enrichme
nts reached 3.5 wt%, and Mn reduction was the only important anaerobic
carbon oxidation process in the upper 10 cm of the sediment. In the l
ess Mn-rich sediments from intermediate depths in the basin, Fe reduct
ion ranged from somewhat less, to far more important than sulfate redu
ction. Most of the Mn reduction in these sediments may have been coupl
ed to the oxidation of acid volatile sulfides (AVS), rather than to di
ssimilatory reduction. High rates of metal oxide reduction at all site
s were driven by active recycling of both Fe and Mn, encouraged by bio
turbation. Recycling was so rapid that the residence time of Fe and Mn
oxides, with respect to reduction, ranged from 70-250 days. These res
ults require that, on average, an atom of Fe or Mn is oxidized and red
uced between 100-300 times before ultimate burial into the sediment. W
e observed that dissolved Mn2+ was completely removed onto fully oxidi
zed Mn oxides until the oxidation level of the oxides was reduced to a
bout 3.8, presumably reflecting the saturation by Mn2+ of highly react
ive surface adsorption sites. Fully oxidized Mn oxides in sediments, t
hen, may act as a cap preventing Mn2+ escape. We speculate that in sha
llow sediments of the Skagerrak, surface Mn oxides are present in a so
mewhat reduced oxidation level (<3.8) allowing Mn2+ to escape, and per
haps providing the Mn2+ which enriches sediments of the deep basin.