A remnant of glacial seawater preserved in the pore fluids of sediment cores from the Maldives Inner Sea provided an opportunity to investigate the stable strontium isotopic composition (δ88/86Sr) of the ocean during the Last Glacial Maximum and explore the usefulness of δ88/86Sr as a tracer of early marine diagenesis. We used paired measurements of δ88/86Sr and radiogenic Sr isotope ratios (87Sr/86Sr) in pore fluids and surrounding carbonate sediments to constrain the diagenetic history of the preserved glacial water mass at IODP Sites U1466 and U1468. These pore fluid profiles document variability in δ88/86Sr in a shallow marine setting, revealing distinct diagenetic processes dominating within different depth intervals. We find evidence for isotope fractionation during secondary calcite precipitation at intermediate depths and observe that in aragonite-dominated settings, fractionation during recrystallization may be obscured by the dissolution of aragonite in the uppermost sediments. Correcting for the effect of carbonate recrystallization on pore fluid Sr concentration ([Sr]) and isotopic composition, we estimate that glacial seawater [Sr] was higher (∼98μM) and δ88/86Sr lower (∼0.32‰) compared to the modern ocean, consistent with hypotheses attributing the present-day disequilibrium of the ocean Sr budget to glacial/interglacial changes in shelf carbonate weathering and burial. Our results provide evidence that the ocean [Sr] and δ88/86Sr are sensitive to carbon cycle changes on timescales much shorter than its residence time (∼2 Myr) and demonstrate that pore fluid δ88/86Sr measurements are a useful addition to multi-tracer studies of diagenesis in complex marine systems.
Read full abstract