Metal and sulfide minerals in ultramafic rocks are ideal tracers for fluid-rock interaction processes. During hydrothermal alteration of ultramafic rocks-the so-called serpentinization reaction where the primary mantle minerals olivine and pyroxene are converted to serpentine, magnetite, talc, and brucite-H 2 is produced due to ferrous iron oxidation McCollom et al., 2016). Simultaneously, H 2 can react abiogenically with CO 2 or CO to produce CH 4 and higher hydrocarbons following Fischer-Tropsch Type and Sabatier reactions (e.g., Etiope et al., 2011). Associated with variations in water-rock ratios during ongoing serpentinization and rock fracturing, this imparts strong variations in fluid redox conditions, i.e., variations in fO 2 , fH 2 , and fS 2 conditions controlling the opaque mineralogy (Foustoukos et al., 2015;Frost, 1985;. Effectively, changes in fO 2 and fS 2 cause precipitation of secondary opaque phases and/ or decomposition of primary mantle sulfides (Alt & Shanks, 1998;Schwarzenbach et al., 2012). In fact, serpentinization environments are among the most reducing environments found on Earth allowing for formation and stabilization of native metals and metal alloys, for example, by desulfurization of magmatic pentlandite (e.g., Frost, 1985;Schwarzenbach, Gazel, & Caddick, 2014). Simultaneously, abiogenically produced H 2 and/or CH 4 as well as other reduced carbon species, produced as a result of the serpentinization process, together with oxidants such as sulfate or CO 2 , provide an ideal energy source for chemolithoautotrophic communities living at sites of active serpentinization (e.g.,