GSA 2020 Connects Online

Paper No. 206-11
Presentation Time: 4:00 PM

IRON CYCLING IN ARCTIC METHANE SEEPS


HONG, Wei-Li1, LATOUR, Pauline2, SAUER, Simone3, SEN, Arunima4, GILHOOLY III, William5, LEPLAND, Aivo6 and FOUSKAS, Fotios5, (1)Department of Geological Sciences, Stockholm University, Svante Arrhenius väg 8, Stockholm, 11418, Sweden; Geological Survey of Norway, Leiv Eirikssons vei 39, Trondheim, 7491, Norway; CAGE-Centre for Arctic Gas Hydrate, Environment and Climate, The Arctic University of Norway in Tromsø, Tromsø, 9010, Norway, (2)Institute for Marine and Antarctic Studies, University of Tasmania, Tasmania, 7004, Australia, (3)Institut Universitaire Européen de la Mer (IUEM), Université de Bretagne Occidentale, Technopôle Brest-Iroise, Rue Dumont d'Urville, Plouzané, 29280, France, (4)Department of Biosciences and Aquaculture, Nord University, Bodø, Bodø, 8049, Norway, (5)Department of Earth Sciences, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, (6)Geological Survey of Norway, Leiv Eirikssons vei 39, Trondheim, 7491, Norway

Anoxic marine sediments contribute a significant amount of dissolved iron (Fe2+) to the ocean which is crucial for the global carbon cycle. Here, we investigate iron cycling in four Arctic cold seeps where sediments are anoxic and sulfidic due to the high rates of methane-fueled sulfate reduction. We estimated Fe2+ diffusive fluxes towards the oxic sediment layer to be in the range of 0.8 to 138.7 μmole/m2/day and Fe2+ fluxes across the sediment-water interface to be in the range of 0.3 to 102.2 μmole/m2/day. Such variable fluxes cannot be explained by Fe2+ production from organic matter–coupled dissimilatory reduction alone. We propose that the reduction of dissolved and complexed Fe3+ as well as the rapid formation of iron sulfide minerals are the most important reactions regulating the fluxes of Fe2+ in these cold seeps. By comparing seafloor visual observations with subsurface pore fluid composition, we demonstrate how the joint cycling of iron and sulfur determines the distribution of chemosynthesis-based biota.