Assessing
Site-Specific Risk to Aquatic Biota from Multiple Exposure Pathways.
Vertucci, F.A.,
Naddy, R.B., and Tillquist, H.T.
ENSR, 4303 W. La Porte Ave., Fort Collins, CO.
Abstract--Many risk assessments rely on ambient water quality
criteria (AWQC) to evaluate potential risks to aquatic biota from contaminant
exposure. The AWQC are not intended
to consider risk from sediment or dietary exposure pathways and few assessments
account for site-specific bioavailability of metals. Risks to a variety of aquatic biota from metals in the Upper
Clark Fork River (UCFR), Montana were evaluated using assessment tools specific
to each exposure medium- water, sediment, and diet. Each medium was evaluated using extensive site-specific
exposure data and, when possible, effects criteria that reflect site-specific
metals bioavailability. Risk from
exposures to water column metals (As, Cd, Cu, Pb and Zn) was evaluated by comparing observed dissolved metals
concentrations (an average of long term monitoring) to chronic AWQC and a
site-specific rainbow trout chronic toxicity reference value (TRV) developed by
EPA based on testing UCFR water. (When environmental concentrations are below
TRV’s, risks are usually assumed nominal.) Sediment metals exposure was
evaluated using EPA draft Equilibrium Sediment Guidelines (ESGs--i.e.,
simultaneously extractable metals - acid-volatile sulfide and sediment porewater
summed as toxic units) and using bulk Sediment Effects Concentrations (SEC)
derived from toxicity tests with UCFR bed sediments.
Trout dietary exposures were addressed by comparing extensive benthic
macroinvertebrate tissue data with dietary TRVs derived from selected
literature. Dissolved metals
concentrations were generally lower than the water column TRVs for each metal.
Metals in pore water and bulk sediments were below ESGs and SECs.
Furthermore, benthic macroinvertebrate tissue concentrations did not
exceed dietary TRVs. These results
predict nominal risk to most UCFR aquatic biota under observed conditions for
each of the exposure pathways evaluated.