The present study investigated the integrated effects of several geochemical processes that control radium-226 ((226) Ra) mobility in the aquatic environment and bioaccumulation in in situ caged benthic invertebrates. Radium-226 bioaccumulation from sediment and water was evaluated using caged oligochaetes (Lumbriculus variegatus) deployed for 10 d in 6 areas downstream of decommissioned uranium operations in Ontario and Saskatchewan, Canada. Measured (226) Ra radioactivity levels in the retrieved oligochaetes did not relate directly to water and sediment exposure levels. Other environmental factors that may influence (226) Ra bioavailability in sediment and water were investigated. The strongest mitigating influence on (226) Ra bioaccumulation factors was sediment barium concentration, with elevated barium (Ba) levels being related to use of barium chloride in effluent treatment for removing (226) Ra through barite formation. Observations from the present study also indicated that (226) Ra bioavailability was influenced by dissolved organic carbon in water, and by gypsum, carbonate minerals, and iron oxyhydroxides in sediment, suggestive of sorption processes. Environmental factors that appeared to increase (226) Ra bioaccumulation were the presence of other group (II) ions in water (likely competing for binding sites on organic carbon molecules), and the presence of K-feldspars in sediment, which likely act as a dynamic repository for (226) Ra where weak ion exchange can occur. In addition to influencing bioavailability to sediment biota, secondary minerals such as gypsum, carbonate minerals, and iron oxyhydroxides likely help mitigate (226) Ra release into overlying water after the dissolution of sedimentary barite. Environ Toxicol Chem 2015;34:507-517. © 2014 SETAC.
Keywords: Bioaccumulation; Bioavailability; Radium-226; Sediment chemistry; Uranium mine.
© 2015 SETAC.