B11I-0554
Key Factors Influencing Rates of Heterotrophic Sulfate Reduction in Hydrothermal Massive Sulfide Deposits

Monday, 14 December 2015
Poster Hall (Moscone South)
Kiana L Frank, University of Hawaii at Manoa, Oceanography, Honolulu, HI, United States, Karyn L Rogers, Rensselaer Polytechnic Institute, Troy, NY, United States, Daniel Rogers, Stonehill College, Chemistry, Easton, MA, United States, David T Johnston, Harvard-Earth & Planet Science, Cambridge, MA, United States and Peter R Girguis, Harvard University, Cambridge, MA, United States
Abstract:
Hydrothermal vents are thermally and geochemically dynamic habitats, and the organisms therein are subject to steep fluctuations in temperature and chemistry. To date, the influence of these environmental dynamics on microbial sulfate reduction has not been well constrained. Here, via multivariate experiments, we evaluate the effects of key environmental variables (temperature, pH, H2S, SO42-, DOC) on sulfate reduction rates and metabolic energy yields in a hydrothermal flange recovered from the Grotto vent in the Main Endeavor Field, Juan de Fuca ridge. Sulfate reduction was measured in batch reactions across a range of physico-chemical conditions. Temperature and pH were the strongest stimuli and maximum sulfate reduction rates were observed at 50°C and pH 6, suggesting that the in situ community of sulfate reducing organisms at Grotto may be most active in a slightly acidic and moderate thermal/chemical regime. At pH 4, sulfate reduction rates increased with sulfide concentrations most likely due to the mitigation of metal toxicity. While substrate concentrations also influenced sulfate reduction rates, energy-rich conditions muted the effect of metabolic energetics on sulfate reduction rates. We posit that variability in sulfate reduction rates reflect the response of the active microbial consortia to environmental constraints on in situ microbial physiology, toxicity, and the type and extent of energy limitation. These experiments help to constrain models of the spatial contribution of heterotrophic sulfate within the complex gradients inherent to hydrothermal deposits.