Geochemical response to pulsed sedimentation: Implications for the use of Mo as a paleo-proxy

Deglacial sediments in piston core JT96-02 from the continental slope off western Canada contain numerous centimeter-thick, iron sulfide-rich layers. Major and minor element chemistry, as well as C and N isotopic data suggest that these layers represent background hemipelagic sedimentation. Intervening gray silty clay layers, each of which exhibits a fining-upward trend, are distal turbidites. The iron sulfides precipitated in response to the emplacement of each turbidite, which slowed oxygen diffusion into the sediment allowing anoxic conditions to develop in the underlying relatively organic-rich deposits. Resulting sulfate reduction and precipitation of Fe-sulfide fostered Mo enrichment (> 2 μg/g). It may also explain Ni, Cr, V, and Co enrichments, although differences in detrital mineralogy cannot be ruled out, particularly for Ni and Cr. Rhenium is also enriched, albeit slightly, within the sulfide layers, but low Re/Mo ratios (~ 0.78 ng/g/μg/g) suggest that anoxic conditions developed very rapidly. Metals with high lithogenic concentrations (Cd and U) are not obviously enriched in the sulfide layers because there was insufficient time for noticeable authigenic accumulation before deposition of the next turbidite which severed diffusive communication with overlying seawater, the primary source of metals. Silver is also slightly higher in the sulfide layers, possibly linked to higher marine organic matter content. In summary, the pulsed character of sedimentation during the deglaciation led to episodic enrichment of Mo and occurred independently of changes in bottom water oxygen or organic carbon content. This observation potentially complicates the use of Mo as a paleo-proxy in some continental margin environments.