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International audience; Pore water and solid phase geochemical profiles of sediment cores collected along two transects on the western and eastern sides of the Mississippi River mouth in the northern Gulf of Mexico were incorporated into a reactive transport model to determine the role of manganese and iron in the remineralization of carbon. Reactive transport model calculations indicate that sedimentation rates control the intensity of anaerobic carbon remineralization and select for the dominant anaerobic carbon remineralization pathways. Although sulfate reduction dominates the shelf station (65 m water depth), denitrification and microbial manganese reduction appear equally significant anaerobic respiration processes along the continental slope the closest to the Mississippi River, whereas microbial iron reduction does not represent an important process in these sediments. These findings suggest that the differential kinetics of manganese and iron redox transformations influence carbon remineralization processes on the continental slope. The fast kinetics of Fe2+ oxidation near the sediment-water interface and high sedimentation rates maintain Fe under the form of Fe(III) oxides and thermodynamically prevent sulfate reduction from dominating carbon remineralization processes on the slope, whereas the much slower Mn2+ oxygenation kinetics allows diffusion of Mn2+ across the sediment-water interface of the shelf station closest to the river mouth. Exposure to oxygenated bottom waters and entrainment within mobile muds typical of deltaic sediments during high riverine discharge likely promote the formation and downslope transport of Mn(III/IV) oxides within the nepheloid layer. This phenomenon appears to form a manganese ‘conveyor belt’ that selectively enriches Mn(III/IV) oxides relative to Fe(III) oxides in the deep sediment. In contrast, the intensity of anaerobic carbon remineralization processes along the eastern continental slope the farthest from the Mississippi River plume is much lower due to the low organic and lithogenic inputs, and denitrification dominates anaerobic respiration. Overall, these findings suggest that manganese cycling and its role in carbon remineralization processes in continental slope sediments exposed to large riverine inputs may be more important than previously considered.

Despite the undeniable effect of iron on shaping patterns of ocean productivity, the relative importance of the different sources of this limiting nutrient to the ocean is still under debate. Although global estimates indicate that the benthic input of iron to the oceans is significant, most studies have investigated continental margins exposed to either upwelling or large riverine inputs, environments that are not representative of the majority of the oceans. Additionally, the number of studies that report dissolved iron concentrations in continental slope sediments is limited, despite the fact that these regions between the shelf edge and the continental rise make up >5% of the sedimentary surface area of the global ocean. The sedimentary flux of iron has traditionally been considered negligible due to the rapid oxidation of Fe2+ in oxic waters and poor solubility of the Fe(III) product. The recent realization that ferric iron may be stabilized in solution by organic ligands during oxidation near the sediment-water interface suggests that a significant fraction of the dissolved iron pool may be present under the form organic-Fe(III) complexes that could eventually reach the overlying waters. In this study, the speciation and biogeochemical importance of iron was determined in intact sediment cores along a transect across the entire continental margin near Cape Lookout, North Carolina, a region not dominated by upwelling or riverine inputs that is representative of most passive continental margins. Rates of diffusive oxygen uptake (DOU) and maximum diffusive fluxes of both dissolved Fe2+and organic-Fe(III) complexes decreased from the coastal zone to the continental shelf, remained low on the shelf and the upper continental slope, but rebounded to reach a maximum in mid-slope sediments where concentrations of Fe(III) oxides were the highest along the transect. In turn, DOU decreased and dissolved iron was below detection in lower-slope sediments, indicating that mid-slope sediments represent depocenters where Fe(III) oxides and organic matter may accumulate. Pore water sulfate and sulfide concentrations as well as separate sediment incubations confirmed that sulfate reduction does not greatly influence the cycling of iron in these sediments. The production of dissolved organic-Fe(III) in these continental margin sediments is likely regulated by a combination of aerobic oxidation in the presence of natural organic ligands near the sediment-water interface, dissimilatory iron reduction, or chemical oxidation of Fe(II) complexed to natural organic ligands. Fluxes of Fe2+ and organic-Fe(III) complexes across the sediment-water interface were not observed. However, diffusive fluxes of Fe2+ and organic-Fe(III) complexes into the oxic zone of these sediments (