Abstract

AbstractThe silicon isotopic composition of silicic acid (δ30Si(OH)4) and biogenic silica (δ30Si‐bSiO2) were measured for the first time in marine Arctic waters from the Mackenzie River delta to the deep Canada Basin in the late summer of 2009. In the upper 100 m of the water column, δ30Si(OH)4 signals (+1.82‰ to +3.08‰) were negatively correlated with the relative contribution of Mackenzie River water. The biogenic Si isotope fractionation factor estimated using an open system model, 30ε = −0.97 ± 0.17‰, agrees well with laboratory and global‐ocean estimates. Nevertheless, the δ30Si dynamics of this region may be better represented by closed system isotope models that yield lower values of 30ε, between −0.33‰ and −0.41‰, depending on how the contribution of sea‐ice diatoms is incorporated. In the upper 400 m, δ30Si‐bSiO2 values were among the heaviest ever measured in marine suspended bSiO2 (+2.03‰ to +3.51‰). A positive correlation between δ30Si‐bSiO2 and sea‐ice cover implies that heavy signals can result from isotopically heavy sea‐ice diatoms introduced to pelagic assemblages. Below the surface bSiO2 production zone, the δ30Si(OH)4 distribution followed that of major water masses. Vertical δ30Si(OH)4 profiles showed a minimum (average of +1.84 ± 0.10‰) in the upper halocline (125–200 m) composed of modified Pacific water and heavier average values (+2.04 ± 0.11‰) in Atlantic water (300–500 m deep). In the Canada Basin Deep Water (below 2000 m), δ30Si(OH)4 averaged +1.88 ± 0.12‰, which represents the most positive value ever measured anywhere in the deep ocean. Since most Si(OH)4 enters the Arctic from shallow depths in the Atlantic Ocean, heavy deep Arctic δ30Si(OH)4 signals likely reflect the influx of relatively heavy intermediate Atlantic waters. A box model simulation of the global marine δ30Si(OH)4 distribution successfully reproduced the observed patterns, with the δ30Si(OH)4 of the simulated deep Arctic Ocean being the heaviest of all deep‐ocean basins.

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