Recycling of surface-derived sulfur into the deep earth can impart distinct sulfur isotope signatures to magmas. The details of sulfur transfer from sedimentary rocks to magmas (and ultimately igneous rocks) through metamorphism and devolatilization and/or partial melting, however, is difficult to trace. To understand this process in detail we studied multiple-sulfur isotope compositions of sulfides in the Archean (c. 2685 Ma) Ghost Lake batholith (GLB) and its surrounding host metasedimentary rocks of the Superior Craton (Ontario, Canada) by high spatial resolution secondary ion mass spectrometry, complemented by high-precision gas source isotope ratio mass spectrometry measurements. The GLB comprises strongly peraluminous biotite+cordierite, biotite+muscovite, and muscovite+garnet+tourmaline granites to leucogranites, which are thought to represent the partial melts of surrounding metagreywackes and metapelites. The metasedimentary rocks display a range of metamorphic grades increasing from biotite-chlorite (280-380 °C) at ∼5 km away from the GLB to sillimanite-K-feldspar grade (∼660 °C) immediately adjacent to the batholith, thus providing a natural experiment to understand sulfur isotope variations from low- to high-grade Archean sedimentary rocks, as well as granites representative of their partial melts.
We find that metasedimentary sulfide δ³⁴S values increase with progressive metamorphism at most 2-3‰ (from −1‰ up to +1 to +2‰). An increase in δ³⁴S values in pyrrhotite during prograde metamorphism can be explained through Rayleigh fractionation during pyrite desulfidation reactions. Pyrite from all but one of the granite samples preserve δ³⁴S values similar to that of the high-grade metasedimentary rocks, indicating that partial melting did not result in significant fractionation of δ³⁴S. The exception to this is one granite sample from a part of the batholith characterized by abundant metasedimentary inclusions. This sample contains pyrite with heterogeneous and low δ³⁴S values (down to −16‰) which likely resulted from incomplete homogenization of sulfur between the granitic melt and metasedimentary inclusions. Small (several tenths of a permil), mostly positive Δ³³S are observed in both the metasedimentary rocks and granites.
Our results suggest that Archean strongly peraluminous granites could be a high-fidelity archive to quantify the bulk sulfur isotope composition of the Archean siliciclastic sediments. Further, our findings indicate that subduction of reduced sulfur-bearing sediments in the Archean with δ³⁴S at or near 0‰ should result in release of sulfur-bearing fluids in the mantle wedge with similar values (within a few permil). S-MIF (if initially present in Archean surface material) may be preserved during this process. However, the absence of S-MIF in igneous rocks does not preclude assimilation of Archean sedimentary material as either S-MIF may not be originally present in the Archean sedimentary sulfur and/or homogenization or dilution could obscure any S-MIF originally present in assimilated Archean sediments
