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Published byWalter Chambers Modified over 9 years ago
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The IAEA EMRAS programme has compared predictions of various models, to each other and to site data. Model-model intercomparison showed considerable variation between models www.ceh.ac.uk/PROTECT Pu-239
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The IAEA EMRAS programme has compared predictions of various models, to each other and to site data Model-model intercomparison showed considerable variation between models Missing value guidance approach often give comparatively high estimates (often for little studied organisms) ‘National’ (site specific) data www.ceh.ac.uk/PROTECT
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H-3, Cs-137, Co-60, Sr- 90 data for wide range of freshwater biota
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www.ceh.ac.uk/PROTECT
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Hopefully have appreciation of how wholebody radionuclide concentrations are estimated in available tools There are some short comings in approaches - not least data availability - but to cover wide range of organism-radionuclide combinations currently ‘best we can do’ Can be considerable variability between models (justify selection) Lack of equilibrium Probably – but if sufficient data should reflect ‘reality’ (e.g. Pu will never reach equilibrium) www.ceh.ac.uk/PROTECT
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Some radionuclides are heterogeneously distributed throughout the body Sr (bone), Am (bone & liver), I (thyroid), Ru (kidney) Uncertainty this adds to dose organ should be assessed (... available effects data are for wholebody dose rates?) If required dynamic models available or scope to adapt from human assessment models If predictions are required spatially - relatively easy to use parameters from models such as ERICA in a GIS www.ceh.ac.uk/PROTECT
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Technical report series Final draft submitted to IAEA On-line database for collation Will be maintained and used to provide annual update tables Database has also been used to collate data for ICRP framework (TG73 report in-press) www.ceh.ac.uk/PROTECT
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