posted on 2007-04-01, 00:00authored byLinda H. Kalnejais, William R. Martin, Richard P. Signell, Michael H. Bothner
The release of particulate-phase trace metals due to
sediment resuspension has been investigated by combining
erosion chamber experiments that apply a range of
shear stresses typically encountered in coastal environments
with a shear stress record simulated by a hydrodynamic
model. Two sites with contrasting sediment chemistry were
investigated. Sediment particles enriched in silver,
copper, and lead, 4−50 times greater than the bulk surface-sediment content, were the first particles to be eroded.
As the shear-stress level was increased in the chamber,
the total mass eroded increased, but the enrichment of these
trace metals fell, approaching the bulk-sediment content.
From the temporal distribution of shear stress generated by
the hydrodynamic model for a site in Boston Harbor,
resuspension fluxes were estimated. The erosion threshold
of this site is exceeded during spring tides, releasing the
particles enriched in trace metals into the water column. Due
to the higher trace metal content and the regularity of
resuspension, low-energy resuspension events (up to a
shear stress of 0.2 N/m2) contribute up to 60% of the
resuspension metal flux in an average year. The estimated
annual quantity of copper and lead resuspended into the
water column is higher than estimates of the total riverine
flux for these metals. These results indicate that sediment
resuspension is a very important mechanism for releasing
metals into the water column and provide new insight into
the chemical and physical processes controlling the long-term fate of trace metals in contaminated sediments.