Description: The Argentina Continental Margin represents a unique geologic setting where fundamental interactions between bottom currents and sediment deposition as well as their impact on biogeochemical processes and element cycling, in particular iron, can be studied. The aims of this study were to investigate 1) the consequences of different depositional conditions on biogeochemical processes and 2) diagenetic cycling of Fe mineral phases in surface sediments. Furthermore, it was 3) studied how sedimentary stable Fe isotope signatures (δ56Fe) are affected during early diagenesis and finally 4) evaluated, under which conditions δ56Fe might be used as proxy for microbial Fe reduction in methanic sediments. During RV SONNE expedition SO260, carried out in the framework of the DFG-funded Cluster of Excellence “The Ocean in the Earth System”, surface sediments from two depositional environments were sampled each using gravity corer and multi corer. One study site is located on the lower continental slope at 3605 m water depth (Biogeochemistry Site), while the other site is situated in a contourite system on the Northern Ewing Terrace at 1078 m water depth (Contourite Terrace Site). Sequential Fe extractions were performed on the collected sediments to determine four operationally defined reactive Fe phases targeting Fe carbonates, (easily) reducible Fe (oxyhydr)oxides and hardly reducible Fe oxides [1]. Purification of extracts for δ56Fe analysis of the Fe carbonates and easily reducible Fe (oxyhydr)oxide fractions followed [2]. The dataset was combined with pore-water data obtained during the cruise and complemented by concentrations and stable carbon isotope signatures of dissolved methane determined post-cruise. The extent of the redox zonation and depth of the sulfate-methane-transition (SMT) differ between the two sites. It is suggested that sedimentation rates at the Biogeochemistry Site are low and that steady state conditions prevail, leading to a strong diagenetic overprint of sedimentary Fe phases. In contrast the Contourite Terrace Site is characterized by high sedimentation rates and a lack of pronounced diagenetic overprint [3]. Reactive Fe phases are subject to reductive dissolution at the SMT. Nevertheless, significant amounts of reactive Fe phases are preserved below the SMT as evidenced by the presence of dissolved Fe in the methanic sediments, and are available for deep Fe reduction possibly through Fe-mediated anaerobic oxidation of methane [4]. In this study, δ56Fe signatures of reactive Fe phases in methanic sediments were determined for the first time. These data suggest significant microbial fractionation of Fe isotopes during deep Fe reduction at the Biogeochemistry Site, whereas at the Contourite Terrace Site the δ56Fe signatures do not indicate remarkable microbial Fe isotope fractionation. It is concluded that the applicability of δ56Fe signatures as tracer for microbial Fe reduction might be sensitive to the depositional regime, and thus may be limited in high sedimentation areas. References: [1]Poulton SW and Canfield DE, 2005. Chemical Geology 214: 209-221. [2]Henkel, S. et al., 2016. Chemical Geology 421: 93-102. [3]Riedinger, N. et al., 2005. Geochimica et Cosmochimica Acta 69: 4117-4126. [4]Riedinger, N. et al., 2014. Geobiology 12: 172-181.

Description: Permeable sandy sediments cover 50-60% of the global continental shelf and are important bioreactors that regulate organic matter (OM) turnover and nutrient cycling in the coastal ocean. In sands, the dynamic porewater advection can cause rapid mass transfer and variable redox conditions, thus affecting OM remineralization pathways as well as the recycling of iron and phosphorus. In this study, North Sea sands were incubated in flow-through reactors (FTRs) to investigate biogeochemical processes under porewater advection and changing redox conditions. We found that the average rate of anaerobic OM remineralization was 12 times lower than the aerobic pathway, and Fe(III) oxyhydroxides were found as the major electron acceptors during 34 days of anoxic incubation. Abundant reduced Fe in the solid phase (expressed as Fe(II)) was measured before extensive Fe2+ release into porewater, and most of the reduced Fe (~96%) remained in the solid phase throughout the anoxic incubation. Fe(II) retained in the solid phase, either through the formation of authigenic Fe(II)-bearing minerals or adsorption, was easily re-oxidized upon exposure to O2 . Excessive P release (apart from OM remineralization) started at the beginning of the anoxic incubation and accelerated after the release of Fe2+ with a constant P/Fe2+ ratio of 0.26. After 34 days of anoxic incubation, porewater was re-oxygenated and 〉99% of released P was coprecipitated through Fe2+ oxidation (so-called “Fe2+ curtain”). Our results demonstrate that Fe(III)/Fe(II) in the solid phase can serve as relatively immobile and rechargeable “redox battery” under dynamic porewater advection. Due to frequent oscillation of redox conditions, the Fe “redox battery” is characteristic for permeable sediments and plays an important role in coastal OM turnover. We also suggest that P liberated before Fe2+ release can escape the “Fe2+ curtain” in porewater advection, thus potentially increasing net benthic P efflux from permeable sediments under variable redox conditions.