Mn(II) carbonate authigenesis marks the benthic SMTZ and is fueled by Mn-driven anaerobic oxidation of methane: A Black Sea evidence

<p>In the Black Sea, sediment cores covering the last brackish-limnic transition were recovered and investigated for anaerobic biogeochemical processes controlling sulfur, carbon, and metal cycling. The development of a sulfate-methane transition zone (SMTZ) is nowadays found below the brackish zone in the limnic part of the sediments that limits the upward migration of biogenic methane into surface sediments and the water column. The position of the SMTZ may have changed in the past due to dynamic fluxes of dissolved species in the pore water. Besides dissolved sulfate, metal-bearing minerals have been shown to serve as potential reactants, also converting CH₄ into dissolved inorganic carbon (DIC). The pore water and sediment stable isotope (C, S, O) and geochemical composition were investigated, as well as in-situ microbial rates of sulfate reduction and total anaerobic oxidation of CH₄ (AOM) obtained from sediment incubations for the identification of a potential contribution of manganese-bearing minerals to AOM in the limnic part of the sediments (Mn-AOM). In the limnic Black Sea sediments Mn-AOM is causes an upward flux of dissolved Mn whereas intense SO₄-AOM located in shalower sediments leads to an increase in pH and a maximum in DIC concentrations in the SMTZ. The resulting change in saturation states leads to the precipitation of mixed MnCa-carbonate solid-solutions (&#8216;rhodochrozitization front&#8217;) and the development of a zone enriched in excess sedimentary Mn(II). We further argue that these authigenic fronts may survive changes in pore water composition and are stable in the anoxic sedimentary record, marking the position of paleo-SMTZs. The persisting formation of this geochemical marker has advantage in application over the transient development of a sulfidization front of metastable mackinawite, that is fromed by the reaction of downard migrating sulfide with upward diffusing Fe(II), originating from SO₄-AOM and Fe-AOM, respectively.</p>