GEOCHEMICAL CONSTRAINTS FOR THE DEPOSITION OF THE DEVONIAN LEICESTER PYRITE MEMBER, WESTERN NEW YORK: IMPLICATIONS FOR THE ACCUMULATION OF DETRITAL SULFIDE DEPOSITS BENEATH AN OXIC ATMOSPHERE
Although the S isotope data are relatively consistent with the proposed model for the deposition of the Leicester Pyrite, fundamental questions remain. First, is the inferred extreme water-column stratification and oxygen depletion supported by independent evidence? Second, what environmental variables ultimately exhumed pyrite from the underlying consolidated Windom Shale while concurrently minimizing both sulfide oxidation and the presence of calcium carbonate bioclasts? Finally, what environmental conditions can be characterized based upon trace metal partitioning within the lag deposit? Addressing geochemical conditions responsible for the formation of the Leicester Pyrite will provide insight into the formation of other geologically significant detrital sulfide deposits.
Constraining depositional controls responsible for the formation of the Leicester Pyrite will assess the validity of applying detrital pyritic lags as proxies for low atmospheric oxygen concentrations. Understanding the fundamental controls governing the formation of metal sulfide deposits will have important implications for the global redox cycling of sulfur and atmospheric oxygen throughout the Proterozoic and Phanerozoic.