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D E Dunning

Publications and source records attributed to D E Dunning.

6 recordsLinked to original sources

Sensitivity and uncertainty studies of the CRAC2 computer code.

We have studied the sensitivity of health impacts from nuclear reactor accidents, as predicted by the CRAC2 computer code, to the following sources of uncertainty: (1) the model for plume rise, (2) the model for wet deposition, (3) the meteorological bin-sampling procedure for selecting weather sequences with rain, (4) the dose conversion factors for inhalation as affected by uncertainties in the particle size of the carrier aerosol and the clearance rates of radionuclides from the respiratory tract, (5) the weathering half-time for external ground-surface exposure, and (6) the transfer coefficients for terrestrial foodchain pathways. Predicted health impacts usually showed little sensitivity to use of an alternative plume-rise model or a modified rain-bin structure in bin-sampling. Health impacts often were quite sensitive to use of an alternative wet-deposition model in single-trial runs with rain during plume passage, but were less sensitive to the model in bin-sampling runs. Uncertainties in the inhalation dose conversion factors had important effects on early injuries in single-trial runs. Latent cancer fatalities were moderately sensitive to uncertainties in the weathering half-time for ground-surface exposure, but showed little sensitivity to the transfer coefficients for terrestrial foodchain pathways. Sensitivities of CRAC2 predictions to uncertainties in the models and parameters also depended on the magnitude of the source term, and some of the effects on early health effects were comparable to those that were due only to selection of different sets of weather sequences in bin-sampling.

Accidents↗

An assessment of health risk from radiation exposures.

A methodology has been developed to assess potential hazards from low-level exposures to radioactive pollutants. Estimates of dose rates to reference organs from internal and external exposure pathways (inhalation of contaminated air, ingestion of contaminated food or water, immersion in contaminated air, and exposure to contaminated ground surfaces) are computed with contemporary dosimetric models. These dose rates are used in a life-table analysis to estimate the radiation-induced cancer deaths and resultant years of life lost in an exposed cohort of 100,000 persons, all simultaneously liveborn and subject to the same risks of dying from competing causes (including natural background radiation). Estimates of the potential health risk are tabulated for approx. 150 radionuclides for each of the exposure pathways; results are summarized in terms of the probability of premature radiation-induced death for a member of the cohort due to incremental radiation exposure, and the average number of years of life lost per incremental fatality. The estimates of radiation-induced mortality generated by these methods provide a useful means of quantifying radiation risk; however, these estimates may be subject to large uncertainties, and can be best interpreted as a measure of the relative degree of hazard associated with exposures to various radionuclides through several exposure pathways.

Actuarial Analysis↗

Imprecision in estimates of dose from ingested 137Cs due to variability in human biological characteristics.

An attempt has been made to quantify the variability in human biological parameters determining dose to man from ingestion of a unit activity of soluble 137Cs and the resulting imprecision in the predicted total-body dose commitment. The analysis is based on an extensive review of the literature along with the application of statistical methods to determine parameter variability, correlations between parameters, and predictive imprecision. The variability in the principal biological parameters (biological half-time and total-body mass) involved can be described by a geometric standard deviation of 1.2-1.5 for adults and 1.6-1.9 for children/adolescents of age 0.1-18 yr. The estimated predictive imprecision (using a Monte Carlo technique) in the total-body dose commitment from ingested 137Cs can be described by a geometric standard deviation on the order of 1.3-1.4, meaning that the 99th percentile of the predicted distribution of dose is within approximately 2.1 times the mean value. The mean dose estimate is 0.009 Sv/MBq (34 mrem/mu Ci) for children/adolescents and 0.01 Sv/MBq (38 mrem/muCi) for adults. Little evidence of age dependence in the total-body dose from ingested 137Cs is observed.

Administration, Oral↗