Reductive deposition of graphite at lithological margins in East Central Vermont: a Sr, C and O isotope study

Abstract

AbstractO, Sr and C isotopes from east‐central Vermont are used to provide information on the timing and volume of metamorphic fluid flow. The results are then used to assess the evidence for redox transformations between C species. Oxygen profiles are homogenised on a metre scale; comparison with Sr isotopes suggest that O alteration may have occurred over a significantly larger timescale than that of Sr, possibly because O was modified during dewatering and diagenesis in addition to the high temperature alteration recorded by strontium. Sr isotope distributions are consistent with cross‐layer fluid fluxes of 104−106 moles m−2; absolute values depend on the Sr fluid‐rock distribution coefficient which is poorly known; however, reaction progress constraints suggest that fluxes were towards the lower end of this range. High δ13C values observed at lithological boundaries cannot be explained by volume loss or closed system processes and are taken to indicate reductive precipitation of graphite as a result of mixing between CO2 and CH4‐bearing fluids. Mass balance calculations indicate that redox reactions occurring under metamorphic conditions convert a minimum of 10% of the CO2 released from limestones into graphite, thus providing a potentially important control on the average residence time of C within the crust with implications for C cycling models.