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The Techa River was contaminated as a result of radioactive releases by the Mayak plutonium production facility in 1949-1956. The residents of riverside communities were exposed to internal irradiation from radionuclides ingested mainly with river water, and also to external gamma irradiation resulting from shoreline and flood-plain contamination. The most important role in population exposure was played by (89,90)Sr and 137Cs. The persons born after the onset of the contamination have been identified as the 'Techa River Offspring Cohort' (TROC). The TROC has the potential to provide direct data on health effects in progeny that resulted from exposure of a general population to chronic radiation. This report describes the results of the calculation of fetal doses due to intakes of radionuclides by their mothers. Particular attention has been given to fetal dose from 90Sr because this nuclide is the most significant in terms of population dose for the Techa River. The comparison of the fetal bone marrow doses evaluated using different approaches proposed in the literature has shown a large dispersal in dose values. The main cause of this is the difference in model assumptions simplifying some developmental aspects of fetal haematopoiesis and bone formation. This paper presents an analysis of these basic assumptions that could be useful for further improvements in fetal dosimetry.

An age- and gender-dependent biokinetic model for strontium was developed based on the study of a population living along the Techa River exposed to effluents from the Mayak Production Association (MPA). To estimate the parameters of a new model (Techa biokinetic model, TBM) many data sets have been assembled: our whole-body counter data on long-term retention of 90Sr in humans, data from studies during the period of global fallout, data resulting from deliberate injection of strontium radionuclides and non-radiological data regarding bone formation and resorption, mineral content of the body, etc. The model was developed using the basic structure of the ICRP biokinetic model for strontium, but new age- and gender-specific parameters were derived. This paper discusses the approaches applied to develop the new model.