Radiological risk from consuming fish and wildlife to Native Americans on the Hanford Site
Author:
Damon Delistraty, Scott Van Verst, and Elizabeth A. Rochette
Date Published:
2009
Description:
Historical operations at the Hanford Site (Washington State,USA) have released a wide array of non-radionuclide and radionuclide contaminants into the environment. As a result of stakeholder concerns, Native American exposure scenarios have been integrated into Hanford risk assessments. Because its contribution to radiological risk to Native Americans is culturally and geographically specific but quantitatively uncertain, a fish and wildlife ingestion pathway was examined in this study.
Adult consumption rates were derived from 20 Native American scenarios (based on 12 studies) at
Hanford, and tissue concentrations of key radionuclides in fish, game birds, and game mammals were
compiled from the Hanford Environmental Information System (HEIS) database for a recent time interval (1995–2007) during the post-operational period. It was assumed that skeletal muscle comprised 90% of in take, while other tissues accounted for the remainder. Acknowledging data gaps, median concentrations of eight radionuclides (i.e., Co-60, Cs-137, Sr-90, Tc-99, U-234, U-238, Pu-238, and Pu-239/240) in skeletal muscle and other tissues were below 0.01 and 1pCi/g wet wt, respectively. These radionuclide concentrations were not significantly different (Bonferroni > P 0.05) on and off the Hanford Site. Despite no observed difference between onsite and offsite tissue concentrations, radiation dose and risk were calculated for the fish and wildlife ingestion pathway using on site data. With median consumption rates and radionuclide tissue concentrations, skeletal muscle provided 42% of the dose, while other tissues (primarily bone and carcass) accounted for 58%. Interms of biota, fish ingestion was the largest contributor to dose (64%). Among radionuclides, Sr-90 was dominant, accounting for 47% of the dose. At median intake and radionuclide levels, estimated annual dose (0.36 mrem/yr) was below a dose limit of 15 mrem/yr recommended by the United States Environmental Protection Agency (USEPA), as well as below a dose limit of 100 mrem/yr proposed by the International Commissionon Radiation Protection (ICRP). Similarly, lifetime cancer risk (1.7E5), calculated with median inputs, was below risk levels corresponding to these dose limits. However, our dose and risk estimates apply to only one pathway within a multidimensional exposure scenario for Native Americans. On the other hand, radiation dose and risk corresponding to onsite tissue concentrations were not significantly different from those corresponding to offsite (background) concentrations. Recognizing uncertainties in exposure and toxicity assessments, our results may facilitate informed decision making and optimize resource allocation within a risk assessment
framework at the Hanford Site.
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