Plutonium,241Am,90sr,and137cs concentrations in some antarctic matrices

A radioecological survey in Antarctica shows that the^239+240Pu,²³⁸Pu,²⁴¹Am,⁹⁰Sr, and¹³⁷Cs activities were detectable in nearly all the samples. The activity level of^239+240Pu,²⁴¹Am, and¹³⁷Cs in antarctic sediments was about 5–20 times lower than in the northern Adriatic Sea sediments, but the²³⁸Pu activities were relatively high. It was interesting to note that the⁹⁰Sr concentrations in all the sediments tended to be low, which could be the result of the easier exchangeable behavior of⁹⁰Sr in water. High concentrations were detected in mosses and lichens and their activity levels were comparable to those in central Italy. The radionuclide ratio analyses show that the major part of^239+240Pu,²⁴¹Am,⁹⁰Sr, and¹³⁷Cs was a result of nuclear weapon tests. The higher²⁴¹Am/^239+240Pu ratio was observed and it could perhaps be the result of fallout of nuclear weapon tests prior to 1962. The²³⁸Pu/^239+240Pu ratio in the antarctic matrices was about seven times higher than in the Northern hemisphere and it could be inferred that the major part of²³⁸Pu was originating from the SNAP-9A satellite accident.     

Radionuclide transfer to marine biota species: review of Russian language studies

An extensive programme of experiments on transfer of radionuclides to aquatic species was conducted in the former USSR starting from the early 1950s. Only a few of these studies were made available in the English language literature or taken into account in international reviews of radionuclide behaviour in marine ecosystems. Therefore, an overview of original information on radionuclide transfer to marine biota species available from Russian language literature sources is presented here. The concentration ratio (CR) values for many radionuclides and for marine species such as: ²³⁹Pu, ¹⁰⁶Ru and ⁹⁵Zr (crustacean), ⁵⁴Mn, ⁹⁰Sr, ⁹⁵Nb, ¹⁰⁶Ru, ¹³⁷Cs ²³⁹Pu, ²⁴¹Am and natural U (molluscs), and ⁵⁴Mn, ⁹⁰Sr, ¹³⁷Cs and ¹⁴⁴Ce (fish) are in good agreement with those previously published, whilst for some of them, in particular, for ³²P and ¹¹⁰Ag (crustaceans), ³⁵S (molluscs), ³²P, ³⁵S, ⁹⁵Nb, and ¹⁰⁶Ru (macroalgae) and ⁶⁰Co and ^239,240Pu (fish) the data presented here suggest that changes in the default CR reference values presented in recent marine reviews may be required. The data presented here are intended to supplement substantially the CR values being collated within the handbook on Wildlife Transfer Coefficients, coordinated under the IAEA EMRAS II programme.     

Influence of clay mineral type and organic matter content on the uptake of239Pu and241Am by plants

Summary The uptake of²³⁹Pu and²⁴¹Am from different clay mineral-organic matter-sand mixtures simulating contrasting soil types was examined in growth chamber experiments. The mixtures represented various combinations of organic matter (0, 5 and 10%), kaolinite (11 type) and montomorillonite (21 type) clay minerals, each at the levels of 5, 10 and 25%, and purified quartz sand (as filler).Results indicated a marked reduction in uptake of both²³⁹Pu and²⁴¹Am with increase in organic matter as well as clay content of the mixtures. The Pu Concentration Ratios (CRs) ranged from (2.5–7.0)×10^–3 in the case of kaolinite-organic matter mixtures, and from (0.9–5.5)×10^–3 in the case of montmorillonite-organic matter mixtures. The corresponding values of Am Concentration Ratios (CRs) obtained were (1.9–725.4)×10^–3 in the case of kaolinite-organic matter mixtures, and between (0.7–3.5)×10^–3 for the montmorillonite-organic matter mixtures.Reduction in the uptake of²⁴¹Am with increasing clay content was more pronounced in the montmorillonite clay-organic matter mixtures as compared to that in the case of kaolinite-organic matter mixtures. While similar qualitative reduction in²³⁹Pu CRs with increasing clay content was observed, the reduction was less marked than in the case of²⁴¹Am. The values for Am CRs were higher than the corresponding Pu CRs in kaolinite based mixtures whereas in the case of montmorillonite-organic matter mixtures Pu CRs exceeded the Am CRs.Increasing organic matter content and its interaction with both kaolinite and montmorillonite clay minerals were found to be equally effective in reducing the uptake of²³⁹Pu as well as²⁴¹Am by plants.     

Long-term development of the radionuclide exposure of murine rodent populations in Belarus after the Chernobyl accident

As a determinant of the associated health risks, the behavior of radionuclides in natural ecosystems needs to be better understood. Therefore, the activity concentration of various long-lived radionuclides released due to the Chernobyl accident, and the corresponding contributions to the whole-body dose rate, was studied as a function of time in mammalian indicator species inhabiting the natural forest ecosystems of Belarus, the bank vole (Clethrionomys glareolus) and the yellow-necked mouse (Apodemus flavicollus). The activity concentrations of ¹³⁷Cs, ¹³⁴Cs, ⁹⁰Sr, ²³⁸Pu, ^239,240Pu, ²⁴¹Pu and ²⁴¹Am in soil and in animals were measured at five monitoring sites with different ground deposition of radionuclides at different distances from the destroyed reactor. The observed temporal pattern of the radionuclide activity concentration in the studied animal populations reflects the changes in biological availability of these isotopes for biota, mostly due to fuel particle destruction and appearance of dissolved and exchangeable forms of radionuclides. The time course of ^134+137Cs activity concentrations in animal populations appeared as a sequence of increase, peak and decrease. Maximal levels of radiocesium occurred 1–2 years after deposition, followed by an exponential decrease. Concentrations of incorporated ⁹⁰Sr increased up to the tenth year after deposition. The activity concentrations of transuranic elements (²³⁸Pu, ^239,240Pu, ²⁴¹Pu and ²⁴¹Am) were much lower than those of the other radionuclides, in the studied animals. A considerable activity of ²⁴¹Am in animals from areas with high levels of contamination was firstly detected 5 years after deposition, it increased up to the tenth year and is expected to increase further in the future. Maximal values of the whole-body absorbed dose rates occurred during the year of deposition, followed by a decrease in the subsequent period. Generally, this decrease was monotonic, mainly determined by the decrease of the external γ-ray dose rate, but there were exceptions due to the delayed maximum of internal exposure. The inter-individual distributions of radionuclide concentrations and lifetime whole-body absorbed doses were asymmetric and close to log-normal, including concentrations and doses considerably higher than the population mean values.     

241Am dating of lake sediments

²⁴¹Am derived from decay of fallout ²⁴¹Pu is now frequently detected in analyses of lake sediments by low-background gamma assay, and offers an alternative to weapons test ¹³⁷Cs in dating recent sediments at those sites where the ¹³⁷Cs record has been degraded by post-depositional mobility or obliterated by Chernobyl fallout. Calculations of the in-growth of ²⁴¹Am from ²⁴¹Pu indicate a nominal distribution broadly similar to that of ¹³⁷Cs, with the maximum ²⁴¹Am activity occuring in fallout dating from 1963. Results from a number of sites suggest that ²⁴¹Am is significantly less mobile in lake sediments than ¹³⁷Cs, and that its distribution in cores reflects more closely the fallout record. Since further decay of existing weapons debris will increase ²⁴¹Am concentrations by about 24% over the next 40 years, ²⁴¹Am is likely to play an increasingly important role in assessing the validity of ²¹⁰Pb dates at sites with varying sediment accumulation rates.     

Natural variation in <Superscript>210</Superscript>Po and <Superscript>210</Superscript>Pb activity concentrations in the urine of Finnish population groups

A study to determine activity concentrations of ²¹⁰Pb and ²¹⁰Po in the urine of certain Finnish population groups was conducted, to investigate the variation in natural background level of urinary excretion. The study participants were divided into three groups mainly based on their diet. The first group comprised recreational fishermen and the second group represented people consuming more reindeer meat than an average Finn, while people using drinking water with very high activity concentrations of ²¹⁰Po were selected for the third group. The fourth group was a control group. The mean urinary excretion of ²¹⁰Po in groups 1 and 2 was 73 and 100 mBq d⁻¹, respectively. These values were higher than the value of the control group (20 mBq d⁻¹) and the mean values reported in the literature. The mean daily urinary excretion of ²¹⁰Pb in groups 1 and 2, 70 and 52 mBq d⁻¹, was also slightly higher than that in the control group (32 mBq d⁻¹). In contrast, the excretion rates of both ²¹⁰Po and ²¹⁰Pb for the members of group 3 were one to two orders of magnitude higher than those reported in the literature. This was clearly due to the elevated levels of natural radionuclides in their drinking water. The present study demonstrates the importance of possessing good knowledge of the background levels, in order to allow the determination of the additional exposure due, for example, to the malevolent use of radiation.     

Studies on the lysosomal binding of 141Ce, 239Np, 239Pu and 241Am in rat and syrian hamster liver using carrier-free electrophoresis

The binding of ¹⁴¹Ce, ²³⁹Np, ¹³⁹Pu and ²⁴¹Am in the liver of rats and Syrian hamsters, following injection in essentially monomeric form, was analyzed by carrier-free electrophoresis at 4–9 days and several months after radionuclide injection. In contrast to density gradient methods lysosomes can be clearly separated from other cell organelles by carrier-free electrophoresis. These, and previous results from this and other laboratories confirm that lysosomes are the main initial binding site for these four radionuclides in the livers of rats and Syrian or Chinese hamsters. Light microscopic autoradiography showed that at all the time intervals studied ²⁴¹Am was more or less uniformly distributed in the liver of all three species. Thus, the changes in the electrophoretic pattern of the nuclides, observed at later time periods in hamsters, cannot be explained by gross redistribution phenomena such as accumulation in macrophages.     

Comparative role of salps and other zooplankton in the cycling and transport of selected elements and natural radionuclides in Mediterranean waters

Salps, salp fecal pellets and other zooplankton species were analyzed for a suite of elements and natural radionuclides to assess their role in the biogeochemical cycling of nuclides in oceanic waters. The nuclide/Al ratios in organisms normalized to the same ratio in crustal rock indicated that Ca, Sr, Zn, Cu, U,²¹⁰Po, and²¹⁰Pb are enriched in the organisms. The concentrations of Fe, Al, Th isotopes and²¹⁰Pb in salps and fecal pellets were about an order of magnitude higher than those in salps, whereas Ca, Cu, Zn, Mn and Po were higher by factors of about 2–5. Fluxes via salp defecation were higher than those which have been measured in crustacean zooplankton species, a result primarily due to the high defecation rates characteristic of salps. High nuclide levels in salp fecal pellets coupled with high defecation rates and presumed high salp biomass in many areas underscore the importance of these indiscriminate filter feeders in packaging and transporting to depth particulate-associated nuclides in surface waters.     

Biosorption of radionuclides by Rhizopus arrhizus

The sorption of various radionuclides viz. 233U, 239Pu, 241Am, 144Ce, 147Pm, 152+154Eu and 95Zr from aqueous nitrate medium has been studied using biomass Rhizopus arrhizus. The biosorption of 233U and 239Pu was found to be maximum at pH 6-7 whereas for other trivalent actinides and fission products viz. 241Am, 144Ce, 147Pm, 152+154Eu and tetravalent 95Zr, it was more effective at pH 2. This biomass is a promising sorbant for the treatment of radioactive effluents from nuclear industry. © Rapid Science Ltd. 1998     

Organic forms of artificial radionuclide compounds in soil solutions from natural biogeocenosis

The date on the distribution of the main radiologicaly important polutants of biosphera (90Sr, 137Cs, 239 + 240Pu, 238Pu, 241Am) over the molecular mass fractions of organic matter in the soil solutions of natural environments are presented. Molecular mass constitution and radionuclide content in the fractions are dependent on radionuclide nature and type of soil and change along the soil profile. The major portion of 238Pu, 239 + 240Pu and 241Am (72-98%) was bound with organic matter in the soil solutions. In the case of organic horizons, these radionuclides were selectively connected with the fractions of high molecular masses (MMw > or = 2000). Radiostrontium is present principally in the fraction of inorganic compounds (19-100%) and in the low molecular mass fraction of organic matter (MMw = 350-500). A selective interaction of 137Cs with organic matter of definite molecular masses was not observed. The radionuclide was found in the "organic" fractions of a wide range of molecular masses (MMw from 350-500 to > or = 18,000) (34-97%) as well as in the fraction of inorganic compounds. The data obtained can provide the theoretical basis for explanation of higher mobility of 90Sr in soil profiles compared to other radionuclides.     

Solubility of airborne radioactive fuel particles from the Chernobyl reactor and implication to dose

Airborne particles of nuclear fuel from the Chernobyl reactor that had been collected on air filters and stored, were characterised using in vitro dissolution tests to assess effective doses after their inhalation. As solvent, the Gamble biological fluid was used to simulate lung fluid. The solubility of the measured radionuclides decreased in the order ¹³⁷Cs>⁹⁰Sr>>²⁴¹Am^239+240Pu in the simulated lung fluid. The dissolution rate constant of e.g. ^239+249Pu ranged from 0.72 to 5.4×10^–6 g·cm^–2 d^–1 and decreased (for all nuclides) with increasing particle size as predicted from theoretical considerations. Considering the inhalation dose, decreasing dose with size and increasing doses with lower solubility may partly counterbalance each other for ¹³⁷Cs and ⁹⁰Sr. On the other hand, for ²³⁹Pu and ²⁴¹Am larger particles and associated lower solubility both change the resulting dose in the same direction towards lower values. The comparison of the experimentally determined dose coefficients with ICRP values indicates that nuclear fuel particles closely resemble type M material characteristics for ¹³⁷Cs and ⁹⁰Sr and type S material characteristics for ²³⁹Pu and ²⁴¹Am.     

The distribution of the radionuclides in the main components of lake ecosystems within the Chernobyl NPP exclusion zone

The results of the studies devoted to the distribution of radionuclides 90Sr, 137Cs, 238Pu, 239 + 240Pu and 241Am in 1998-2003 in main components of Glubokoe Lake and Dalekoe-1 Lake located within Krasnensky flood lands of the Pripyat River (inner exclusion zone of the Chernobyl NPP) were analysed. The data about the radionuclide content in bottom sediments, in water, in seston, in macrozoobenthos (including bivalvia molluscs), in gasteropods molluscs, in higher aquatic plants and in fish are presented.     

Comparative assessment of the danger of inhaling 239Pu and 241Am based on the degree of leukopenia in dogs

From the analysis of the results of examination of 96 dogs it is concluded that the estimate of a relative danger of breathing transuranium radionuclides with different metabolism rates (polymeric 239Pu and monomeric 241Am), according to degree of leukopenia is more reliable when it is compared with a mean weighed dose per whole organism than the dose per individual "critical" organ.     

Assessment of the exposure pathway in the uptake and distribution of americium and cesium in cuttlefish (Sepia officinalis) at different stages of its life cycle

Laboratory radiotracer experiments were performed to study the uptake, assimilation and retention of americium (²⁴¹Am) and cesium (¹³⁴Cs) by the common cuttlefish Sepia officinalis. Uptake and loss kinetics of the radionuclides were measured following exposure through sediments, seawater and food at different stages of the animal's life cycle. Sediment was found to be a minor uptake pathway for both radionuclides in juveniles. Following a short seawater exposure, cuttlefish accumulated ²⁴¹Am and ¹³⁴Cs, but only to a limited extent (whole-body CF < 2). Among the cuttlefish organs, branchial hearts and their appendages displayed the highest degree of uptake for ²⁴¹Am (CF = 42 and 16, respectively), but these tissues contained low percentage of total ²⁴¹Am due to their relatively small contribution to whole organism weight. The major fraction of incorporated radionuclides was associated with muscular tissues (viz. 65% and 82% of total ²⁴¹Am and ¹³⁴Cs, respectively). Whole-body loss of ²⁴¹Am and ¹³⁴Cs was relatively rapid (T_b½ = 14 and 6 days, respectively). After dietary exposure, around 60% and 30% of ingested ²⁴¹Am was assimilated into the tissues of juvenile and adult cuttlefish, respectively. However, assimilated ²⁴¹Am was more strongly retained in adults than in juveniles (T_b½ = 28 vs. 5 days, respectively), suggesting that different mechanisms govern ²⁴¹Am elimination at both ages. Ingested ¹³⁴Cs was assimilated to a similar extent in juveniles (29%) and adults (23%), but the depuration rate was four times faster in adults. Our results strongly suggest that these two radionuclides follow different excretion pathways and that the mechanisms can vary with age for a given radionuclide.     

Self-renewal capacity of murine hemopoietic stem cells under internal contamination with239Pu and241Am

Summary The self-renewal capacity of murine pluripotent hemopoietic stem cells (CFU-S) of vertebral bone marrow was studied under conditions of short-term and long-term internal contamination with²³⁹Pu or²⁴¹Am in female mice. Measurement of the CFU-S self-renewal capacity was carried out using double transplantation assay. To evaluate the production of differentiated progeny of stem cells average erythroblast numbers/visible spleen colony and⁵⁹Fe-uptake/colony were computed. The marrow cellularity/vertebra and the number of CFU-S/vertebra were decreased and affected more by²³⁹Pu than by²⁴¹Am. The production of erythroblasts per a single CFU-S and the⁵⁹Fe-uptake/colony were reduced, similarly the numbers of secondary spleen colonies and of secondary CFU-S in primary colonies. The above changes resulting from impaired functions of surviving CFU-S were more serious with²⁴¹Am than with²³⁹Pu. The biological effects of plutonium and americium appeared independent of the phase of contamination.     

Comparison of chronic low-dose effects of alpha- and beta-emitting radionuclides on marine bacteria

Effects of Americium-241 (²⁴¹Am), alpha-emitting radionuclide of high specific radioactivity, and tritium (³H), beta-emitting radionuclide, on luminous bacteria Photobacterium phosphoreum were compared. Bioluminescence intensity served as a marker of bacterial physiological activity. Three successive stages in the bioluminescence response to ²⁴¹Am and ³H were found under conditions of lowdose irradiation: (1) absence of effects, (2) activation, and (3) inhibition. They were interpreted in terms of bacterial response to stressfactor as stress recognition, adaptive response/syndrome, and suppression of physiological function (i.e. radiation toxicity). Times of bioluminescence activation (TBA) and inhibition (TBI) were suggested as parameters to characterize hormesis and toxic stages in a course of chronic low-dose irradiation of the microorganisms. Values of TBA and TBI of ²⁴¹Am were shorter than those of ³H, revealing higher impact of alpha-irradiation (as compared to beta-irradiation) under comparable radiation doses. Increases of peroxide concentration and NADH oxidation rates in ²⁴¹Am aquatic solutions were demonstrated; these were not found in tritiated water. The results reveal a biological role of reactive oxygen species generated in water solutions as secondary products of the radioactive decay. The study provides a scientific basis for elaboration of bioluminescence-based assay to monitor radiotoxicity of alpha- and beta-emitting radionuclides in aquatic solutions.     

Transfer of radionuclides to ants, mosses and lichens in semi-natural ecosystems

There is a scarcity of data on transfer of both natural and anthropogenic radionuclides to detritivorous invertebrates for use in the assessment of radiation exposure. Although mosses and lichens have been extensively used in biomonitoring programs, the data on transfer of radionuclides to these species are limited, particularly for natural radionuclides. To enhance the available data, activity concentrations of ¹³⁷Cs, ²²⁶Ra and ²²⁸Ra were measured in ants, mosses and lichens and corresponding undisturbed soil collected from semi-natural ecosystems in Serbia and Montenegro and biota/soil concentration ratios (CR) calculated. Since the majority of internal dose to biota is expected to come from ⁴⁰K, the activity concentrations of this radionuclide were also determined. The mean CR values for ¹³⁷Cs, ²²⁶Ra and ²²⁸Ra in ants analyzed in this study were found to be 0.02, 0.06 and 0.02, respectively. The mean CR values of radionuclides in mosses were found to be 2.84 for ¹³⁷Cs, 0.19 for ²²⁶Ra and 0.16 for ²²⁸Ra, while those in lichens were found to be 1.08 for ¹³⁷Cs, 0.15 for ²²⁶Ra and 0.13 for ²²⁸Ra. The CR values obtained in this study were compared with default CR values used in the ERICA Tool database and also with those reported in other studies.     

Solid–Aqueous Phase Partitioning of Radionuclides by Complexing Compounds Excreted by Subsurface Bacteria

Radionuclides are present in numerous aerobic and anaerobic subsurface environments due to nuclear weapons testing, leakage from process and storage facilities, and discharge of radioactive waste. The partitioning of radionuclides between liquid and solid phases by complexing compounds excreted by subsurface bacteria was studied. The solid–aqueous phase partitioning of pico- to submicromolar amounts of ⁵⁹Fe, ¹⁴⁷Pm, ²³⁴Th, and ²⁴¹Am was analyzed in the presence of quartz sand and exudates from three species of subsurface bacteria: Pseudomonas fluorescens, Pseudomonas stutzeri, and Shewanella putrefaciens. All were grown under aerobic conditions, and P. stutzeri and S. putrefaciens were grown under anaerobic conditions as well. The supernatants of the aerobic and anaerobic cultures were collected and radionuclide was added. Quartz sand, with a Brunauer, Emmett, and Teller (BET) surface area of 0.1 m² g^–1, was added to the supernatant radionuclide mix, and the pH was adjusted to approximately 8. After centrifuging, the amount of radionuclide in the liquid phase of the samples and controls was analyzed using scintillation. Relative to the control, aerobic supernatants maintained more than 50% of the added ⁵⁹Fe, ²³⁴Th, and ²⁴¹Am. The highest amount of metal present in the liquid phase of the anaerobic supernatants was found in the case of ²⁴¹Am, with 40% more ²⁴¹Am in samples than in controls. Both aerobic and anaerobic supernatants tested positive for complexing compounds when analyzed using the Chrome Azurol S assay. The great amounts of radionuclides in the liquid phases of samples were likely due to complexation with such compounds. Bacterially excreted complexing compounds hence seem able to influence the solid–aqueous phase partitioning of radionuclides. This could influence the mobility of radionuclides in contaminated subsurface environments.     

Comparative studies on the lysosomal association of monomeric 239Pu and 241Am in rat and Chinese hamster liver: analysis with sucrose, metrizamide, and Percoll density gradients of subcellular binding as dependent on time

The binding of 239Pu and 241Am in the livers of Chinese hamsters and rats was analyzed by centrifugation of a mitochondrial-lysosomal fraction in sucrose, metrizamide, and Percoll density gradients at intervals between 4 and 70 days after nuclide injection. The behavior of 239Pu and 241Am during the centrifugation experiments was very similar. In contrast to the results for rats, the median densities of the nuclide profiles from hamsters decrease with time in hyperosmolar sucrose gradients, as does the nuclide fraction liberated by addition of Triton X-100, and the nuclide profiles do not respond typically to Triton WR 1339 treatment of the animals. The results with nearly iso- osmolar metrizamide gradients, together with those for Percoll, agree with the assumption that there is an initial lysosomal association of the transuranium elements. It was concluded from the results that the major fraction of 239Pu and 241Am remained bound to typical lysosomes in rat liver, whereas those in hamster liver may be transformed into telolysosomes . Possibly, a vesicular biliary transport system for certain heavy metals, for which evidence exists in rat liver, does not occur in Chinese hamster liver.     

Sorption of plutonium, americium and fission products from reprocessing effluents using Rhizopus arrhizus

Rhizopus arrhizus biomass removed more than 95% of 239Pu, 241Am, 95Zr, 144Ce and 152+154Eu from different waste streams generated in Purex as well as Truex processes after suitable adjustment of pH. © Rapid Science Ltd. 1998