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Plutonium in daily diet in Poland after the Chernobyl accident.

The content of 239,240Pu was determined in the daily diet collected in northeastern Poland (Bialystok) from March 1987 to May 1992. The estimated annual intake of plutonium decreased from 774 mBq y-1 in the first year after the Chernobyl accident down to approximately 90 mBq y-1 in the sixth year. Large fluctuations of daily intake in the first 2 y suggested that a large fraction of plutonium in the daily diet originated from the external contamination. Assuming the fractional absorption factor of 10(-5) for externally contaminated foodstuffs and 10(-3) for root uptake, the assimilated 239,240Pu would be in the range from approximately 0.02 mBq up to approximately 2 mBq for the period studied.

Accidents↗

Contributions of Rocky Flats releases to the total plutonium in regional soils.

Total 239,240Pu and the 240Pu:239Pu atom ratio were measured in soil samples from around the Rocky Flats Environmental Technology Site (RFETS) during 1992-1994. Mass isotopic data provided a sensitive technique to resolve low levels of RFETS 239,240Pu superimposed on plutonium from global fallout. Concentrations of 239,240Pu within this sample set ranged from 1.1 Bq kg(-1) offsite to 57 Bq kg(-1) onsite, and the 240Pu:239Pu atom ratio increased from 0.055 onsite to 0.123 at approximately 19 km east of the RFETS boundary. The relationship between 24OPu:239Pu atom ratios and distance indicated that a measurable RFETS contribution may have extended to > or = 19 km offsite in the easterly direction. Although the RFETS contribution to total plutonium at the offsite locations ranged from 24-90%, the overall inventory was relatively small. Total inventory estimates, for one transect, based on 239,240Pu and from 240Pu:239Pu atom ratio measurements were not significantly different.

Colorado↗

Gastrointestinal absorption of plutonium by the Marshall Islanders.

The gastrointestinal absorption constant (f1) is a critical parameter in assessing systemic uptake following the ingestion of a radioactive material and in monitoring such intakes. This study addresses the latter, particularly for plutonium, and from environmental measurements derives an f1 value of 4 x 10(-4) for the Marshallese population. The uncertainty associated with the methodology and measurements used in this f1 value assessment is evaluated. This evaluation takes into account the results from 24-h urine samples and the particular lifestyle of the Marshallese. Plutonium intake resulting from soil consumption is a primary parameter in this evaluation; for this study, it was assumed to be 500 mg d(-1). The f1 value determined here is consistent with the values in ICRP Publication 67 of 5x10(-4) for ages 1 to adult, and is the same as that suggested by the NRPB.

Adolescent↗

Siting criteria based on the prevention of deterministic effects from plutonium inhalation exposures.

Siting criteria are established by regulatory authorities to evaluate potential accident scenarios associated with proposed nuclear facilities. The 0.25 Sv (25 rem) siting criteria adopted in the United States has been historically based on the prevention of deterministic effects from acute, whole-body exposures. The Department of Energy has extended the applicability of this criterion to radionuclides that deliver chronic, organ-specific irradiation through the specification of a 0.25 Sv (25 rem) committed effective dose equivalent siting criterion. A methodology is developed to determine siting criteria based on the prevention of deterministic effects from inhalation intakes of radionuclides which deliver chronic, organ-specific irradiation. Revised siting criteria, expressed in terms of committed effective dose equivalent, are proposed for nuclear facilities that handle primarily plutonium compounds. The analysis determined that a siting criterion of 1.2 Sv (120 rem) committed effective dose equivalent for inhalation exposures to weapons-grade plutonium meets the historical goal of preventing deterministic effects during a facility accident scenario. The criterion also meets the Nuclear Regulatory Commission and Department of Energy Nuclear Safety Goals provided that the frequency of the accident is sufficiently low.

Air Pollution, Radioactive↗

The impact of plutonium speciation on the distribution coefficients in a sediment-sea water system, and radiological assessment of doses to humans.

When radionuclides are released from a source into the marine environment, the assessment of long term consequences to humans depends on information on the source term, transport in water, interactions with sediments (KD) and biological uptake (CF). Sensitivity analysis of assessment models demonstrates that KD is one of the most sensitive parameters contributing to large uncertainties in the assessment. Furthermore, the interaction of Pu-species with sediments is a time and temperature dependent process. The distribution coefficient, Bq kg(-1) sediment per Bq L(-1) sea water, increases with time until pseudo-equilibrium/equilibrium is reached (KD). Thus, the contact time between contaminated sea water and sediments should be taken into account in dispersion and dose assessment models. In the present work, dynamic tracer experiments have been performed where different Pu-species are added to a sediment-sea water system to obtain information on KD's. After a defined contact time, the samples have been sequentially extracted to determine mobile and bound fractions. The results indicate that the distribution coefficient, KD, for plutonium depends on Pu-species in question. Thus, sediments act as a sink for Pu(III, IV) (high KD), while Pu(III, IV)-organic and Pu(V, VI) should be considered more mobile (low KD). Furthermore, the interaction with inert fractions obtained from sequential extraction depends less on Pu-species but increase with time. For short time interactions, species-specific time functions rather than KD constants should be applied in assessment models. When the accepted KD (10(5) L kg(-1)) is implemented in the model, the estimated collective dose is about 8 x 10(-4) person-Sv, i.e., a factor of about 2 lower than for Pu(III, IV)-organic and Pu(V, VI). So changes in KD have an impact on the assessment of collective dose received from a potential release of plutonium from fallout, reactor accidents, etc., which underlines the need for more detailed studies on speciation, kinetics, and KD's in different sediment-sea water systems.

Acetates↗

Internal dosimetry of plutonium using the late urinary excretion.

An attempt has been made to standardize the methodology of internal dose computation from the late urinary excretion data. The methodology was selected keeping in mind the most recent ICRP publications and the results of internal dosimetry intercomparison studies reported in literature. The key element of this methodology is the PC-based computational software LUDEP 2.05, which implements the new model of the human respiratory tract. Late urinary excretion data of three male subjects involved in accidental intakes of plutonium aerosols more than 25 years ago were interpreted in terms of intakes and internal doses with the aid of the standardized methodology. An important implication of this work is that late urinary excretion data of the occupational workers of any plutonium handling facility could be used to show the compliance with the life-time dose limit.

Aerosols↗

The quality evaluation program for plutonium pits at the U.S. DOE Pantex plant.

The United States Department of Energy Pantex Plant quality evaluation program for plutonium pits is an extensive program that includes 1) weigh and leak check system; 2) radiography; and 3) dye penetrant testing. Successful completion of these diagnostics qualifies a pit to remain in the active status stockpile program. The use of lead aprons and a robot when handling the plutonium pits minimizes personnel exposures to ionizing radiation. All personnel exposures to ionizing radiation at Pantex Plant are As Low As Reasonably Achievable.

Humans↗

High-resolution autoradiography of intracellular plutonium.

Intracellular incorporation of polymeric plutonium injected into mice was demonstrated in liver and spleen by electron-microscopic auto-radiography. The observations are not inconsistent with other evidence indicating the association of plutonium with lysosomal components. Early results with a quantitative electron-microscopic technique may lead to microdosimetry of cells and cellular components.

Animals↗

Intracellular plutonium: removal by liposome-encapsulated chelating agent.

Chelating agents, such as ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA) were successfully encapsulated within lipid spherules (that is, liposomes). Encapsutlated [(14)C]EDTA, given intravenously to mice, was retained longer in tissues that nonencapsulated [(14)C]EDTA. Encapsulated DTPA, given to mice 3 days after pluttonium injection, removed an additional fraction of plutonium in the liver, presumably intracellular, not available to nonencapslulated DTPA. It also further increased urinary excretion of plutonium. Introduction of chelating agents into cells by liposomal encapsulation is a promising new approach to the treatment of metal poisoning

Animals↗

Radioactive waste: the problem of plutonium.

Systems under development for the recovery of plutonium from spent fuel and its recycling in fresh fuel would not significantly reduce either the total alpha-activity or the amount of fissile plutonium in radioactive waste relative to what is possible with once-through fuel cycles.

Animals↗

Plutonium-induced proliferative lesions and pulmonary epithelial neoplasms in the rat: immunohistochemical and ultrastructural evidence for their origin from type II pneumocytes.

Immunohistochemistry and transmission electron microscopy were used to clarify the cellular origin for plutonium-239-induced pulmonary proliferative (preneoplastic) epithelial lesions and epithelial neoplasms in F344 rats. Examples of each histologic type of proliferative lesion and neoplasm were stained by the avidin-biotin complex immunoperoxidase method using antibodies to rat surfactant apoprotein and Clara cell antigen. Rat surfactant apoprotein immunostaining was detected in type II pneumocytes in sections of normal lung, in the cells of the proliferative lesions classified histologically as alveolar epithelial hyperplasia (51) and mixed foci (alveolar epithelial hyperplasia with fibrosis) (30), and in adenomas (2), adenocarcinomas (3), and adenosquamous carcinomas (2). With the exception of one adenosquamous carcinoma, Clara cell antigen immunostaining was not detected in any of the pulmonary lesions but was detected in nonciliated cuboidal epithelial (Clara) cells in normal bronchioles. The epithelial cells of the proliferative lesions and neoplasms had ultrastructural features consistent with type II pneumocytes, i.e., the presence of cytoplasmic lamellar and multivesicular bodies. The results of these studies indicate that the majority of plutonium-induced proliferative epithelial lesions and neoplasms in the rat originate from alveolar type II pneumocytes.

Animals↗

Improving estimates of exposures for epidemiologic studies of plutonium workers.

Epidemiologic studies of nuclear facilities usually focus on relations between cancer and doses from external penetrating radiation, and describe these exposures with little detail on measurement error and missing data. We demonstrate ways to document complex exposures to nuclear workers with data on external and internal exposures to ionizing radiation and toxic chemicals. We describe methods for assessing internal exposures to plutonium and external doses from neutrons; the use of a job exposure matrix for estimating chemical exposures; and methods for imputing missing data for exposures and doses. For plutonium workers at Rocky Flats, errors in estimating neutron doses resulted in underestimating the total external dose for production workers by about 16%. Estimates of systemic deposition do not correlate well with estimates of organ doses. Only a small percentage of workers had exposures to toxic chemicals, making epidemiologic assessments of risk difficult.

Colorado↗

[The specificity of the deposition of intratracheally administered plutonium in different skeletal bones with a change in iron homeostasis].

A study was made of the distribution of plutonium-239 injected intratracheally within different bones of the skeleton, the iron status in the blood being changed. The iron preparation caused a 2.5-3-fold decrease in the plutonium loading onto cancellous bone tissue that displayed, in ordinary conditions, a higher tropism to the radionuclide than a cortical highly mineralized bone did.

Animals↗

[The levels of soil pollution with plutonium isotopes in the Bryansk Oblast (following the accident at the Chernobyl Atomic Electric Power Station)].

The estimates of plutonium concentration in soils of Western regions of Bryansk (Krasnogorsky, Novozybkovsky, Zlynkovsky and Klintsovsky) are presented. The levels of soil contamination with plutonium within the regions examined vary by 4-5 times, although no definite geographical direction of pollution intensity within the territory examined is noted. The cumulative concentration of isotopes (238Pu, 239Pu, and 240Pu) varies within 21-112 Bq/kg.

Accidents↗

[Effect of liposome-encapsulated pentacin on plutonium-239 excretion].

A study was made of the influence of pentacin, encapsulated in liposomes, on the excretion of monomeric plutonium-239 from dogs and albino rats. Pentacin in a liposomal form, in comparison with free pentacin, increased the excretion of plutonium in urine from a dog body by 23.5% when administered in 24 h, and by 28% when administered in 20 days; in rats, the excretion increase made 40% after the administration in 30 or 45 days.

Animals↗

[Distribution of plutonium in the body of rats after its intratracheal administration in the form of a Pu(IV)-TBP complex].

Tributyl phosphate intratracheally administered to rat body with a Pu(IV)-TBP complex does not increase the accumulation of plutonium in the skeleton and liver. Plutonium is excreted from the lungs more readily than Pu(IV) nitrate and its large amounts are resorbed in the blood early after the administration; its excretion in feces is approximately 100 times more intense than in urine.

Administration, Inhalation↗