Abstract

Abstract. Expanding hypoxia in the Baltic Sea over the past century has led to the development of anoxic and sulfidic (euxinic) deep basins that are only periodically ventilated by inflows of oxygenated waters from the North Sea. In this study, we investigate the potential consequences of the expanding hypoxia for manganese (Mn) burial in the Baltic Sea using a combination of pore water and sediment analyses of dated sediment cores from eight locations. Diffusive fluxes of dissolved Mn from sediments to overlying waters at oxic, hypoxic and euxinic sites are consistent with an active release of Mn from these areas. Although the present-day fluxes are significant (ranging up to ca. 240 μmol m−2 d−1), comparison to published water column data suggests that the current benthic release of Mn is small when compared to the large pool of Mn already present in the hypoxic and anoxic water column. Our results highlight two modes of Mn carbonate formation in sediments of the deep basins. In the Gotland Deep area, Mn carbonates likely form from Mn oxides that are precipitated from the water column directly following North Sea inflows. In the Landsort Deep, in contrast, Mn carbonate and Mn sulfide layers appear to form independently of inflow events, and are possibly related to the much larger and continuous input of Mn oxides linked to sediment focusing. Whereas Mn-enriched sediments continue to accumulate in the Landsort Deep, this does not hold for the Gotland Deep area. Here, a recent increase in euxinia, as evident from measured bottom water sulfide concentrations and elevated sediment molybdenum (Mo), coincides with a decline in sediment Mn content. Sediment analyses also reveal that recent inflows of oxygenated water (since ca. 1995) are no longer consistently recorded as Mn carbonate layers. Our data suggest that eutrophication has not only led to a recent rise in sulfate reduction rates but also to a decline in reactive Fe input to these basins. We hypothesize that these factors have jointly led to higher sulfide availability near the sediment–water interface after inflow events. As a consequence, the Mn oxides may be reductively dissolved more rapidly than in the past and Mn carbonates may no longer form. Using a simple diagenetic model for Mn dynamics in the surface sediment, we demonstrate that an enhancement of the rate of reduction of Mn oxides is consistent with such a scenario. Our results have important implications for the use of Mn carbonate enrichments as a redox proxy in marine systems.

Highlights

  • Manganese (Mn) enrichments in brackish and marine sedimentary deposits can be used as an indicator of redox changes in the overlying waters (e.g. Calvert and Pedersen, 1993)

  • We investigate the potential consequences of the expanding hypoxia for manganese (Mn) burial in the Baltic Sea using a combination of pore water and sediment analyses of dated sediment cores from eight locations

  • The pore waters are supersaturated with respect to Mn carbonate below the surface sediment at the Landsort Deep

Read more

Summary

Introduction

Manganese (Mn) enrichments in brackish and marine sedimentary deposits can be used as an indicator of redox changes in the overlying waters (e.g. Calvert and Pedersen, 1993). Mn carbonate minerals are suggested to form from Mn oxides deposited during periods of bottom water oxygenation (Calvert and Pedersen, 1996; Huckriede and Meischner, 1996), with. Sediment Mn data for both the Landsort Deep in the Baltic Sea (Lepland and Stevens, 1998) and the Black Sea (Lyons and Severmann, 2006) indicate that Mn enrichments may form in sediments overlain by continuously anoxic bottom waters. In the Landsort Deep, these enrichments consist of both Mn carbonates and Mn sulfides (Lepland and Stevens, 1998; Suess, 1979). A better understanding of the various modes of formation of sedimentary Mn and the link with variations in bottom water redox conditions is essential when interpreting Mn enrichments in geological deposits (e.g. Calvert and Pedersen, 1996; Huckriede and Meischner, 1996; Jones et al, 2011; Meister et al, 2009)

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call