During the past two decades, the isotope ratios of numerous redox-sensitive metals in sedimentary archives (particularly organic-rich mudrocks, carbonates, and iron formations) have emerged as valuable tools for constraining changes in global oceanic redox conditions. The long modern ocean residence times of Mo (~440 kyr; Miller et al., 2011), U (~450 kyr; Dunk et al., 2002), and Tl (~20 kyr;Nielsen et al., 2017) relative to ocean mixing times (~1-2 kyr; Sarmiento & Gruber, 2006), together with the distinctive isotope fractionations observed for metal removal into diverse marine sinks, means that the isotopic composition of these metals can serve as global oceanic redox tracers. Redox-sensitive metal isotopes have become an attractive tool with which to place constraints on the magnitude of oceanic anoxia associated with the emplacement of LIPs. The overarching approach is to use sedimentary rocks (organic-rich mudrocks for Mo, U, and Tl; carbonates for U) to infer the isotopic composition of coeval global seawater before, during, and after LIP emplacement, and employ isotopic mass