Redox-controlled iron isotope fractionation during magmatic differentiation: An example from the Red Hill intrusion, S. Tasmania

This study presents accurate and precise iron isotopic data for 16 co-magmatic rocks and 6 pyroxene-magnetite pairs from the classic, tholeiitic Red Hill sill in southern Tasmania. The intrusion exhibits a vertical continuum of compositions created by in situ fractional crystallisation of a single injection of magma in a closed igneous system and, as such, constitutes a natural laboratory amenable to determining the causes of Fe isotope fractionation in magmatic rocks. Early fractionation of pyroxenes and plagioclase, under conditions closed to oxygen exchange, gives rise to an iron enrichment trend and an increase in fo₂ of the melt relative to the Fayalite-Magnetite-Quartz (FMQ) buffer. Enrichment in Fe³⁺/ΣFe_melt is mirrored by δ⁵⁷Fe, where ^VIFe²⁺-bearing pyroxenes partition ⁵⁷Fe-depleted iron, defining an equilibrium pyroxene-melt fractionation factor of Δ⁵⁷ Fe_px-melt ≤ -0.25‰ × 10⁶/T² Upon magnetite saturation, the fo₂ and δ⁵⁷Fe of the melt fall, commensurate with the sequestration of the oxidised, ⁵⁷Fe-enriched iron into magnetite, quantified as Δ⁵⁷ Fe_mtn-melt= +0.20‰ × 10⁶/T² Pyroxene-magnetite pairs reveal an equilibrium fractionation factor of Δ⁵⁷ Fe_mtn-px= ≈ + 0.30‰ at 900-1,000 °C. Iron isotopes in differentiated magmas suggest that they may act as an indicator of their oxidation state and tectonic setting.