The concentration of Cs in the surface of the Greek marine environment

The radiological status of the Greek marine environment, prior to the Chernobyl accident, was characterized mainly by the fallout from nuclear weapon tests. However, the release of radioactivity into the environment from the accident in the Chernobyl Nuclear Power Plant and its deposition in the Greek marine environment resulted in an increase of the ¹³⁷Cs activity concentration by approximately one order of magnitude. In addition, the direct transport of radiocaesium into the North Aegean Sea has been further influenced by the late impact of the Chernobyl accident on the Greek marine environment, related to the transfer of ¹³⁷Cs, mainly through the Dnieper but also the Danube rivers, to the Black Sea and further to the North Aegean Sea through the Straits of Dardanelles. The aim of this work is to provide a present day picture of the geographic variation of the concentration of ¹³⁷Cs in the surface layer of the Greek marine environment and hence, to evaluate the annual committed effective dose delivered to humans through the ingestion pathway from marine sources.     

Fractionation of radionuclide species in the environment

Naturally occurring and artificially produced radionuclides in the environment may be present in different physico-chemical forms (i.e., radionuclide species) varying in size (nominal molecular mass), charge properties and valence, oxidation state, structure and morphology, density, degree of complexation, etc. Low molecular mass (LMM) species are believed to be mobile and potentially bioavailable, while high molecular mass (HMM) species such as colloids, polymers, pseudocolloids and particles are considered inert. Due to time-dependent transformation processes such as mobilisation of radionuclide species from solid phases or interactions of mobile and reactive radionuclide species with components in soils and sediments, the original distribution of radionuclides deposited in ecosystems will change over time. To assess the environmental impact from radionuclide contamination, information on radionuclide species deposited, interactions within affected ecosystems and the time-dependent distribution of radionuclide species influencing mobility and biological uptake is essential. The development of speciation techniques to characterize radionuclide species in waters, soils and sediments should therefore be essential for improving the prediction power of impact and risk assessment models. The present paper reviews available fractionation techniques which can be utilised for radionuclide speciation purposes.     

The role of physical processes controlling the behaviour of radionuclide contaminants in the aquatic environment: a review of state-of-the-art modelling approaches

This paper is aimed at presenting and discussing the methodologies implemented in state-of-the-art models for predicting the physical processes of radionuclide migration through the aquatic environment, including transport due to water currents, diffusion, settling and re-suspension. Models are briefly described, model parameter values reviewed and values recommended. The different modelling approaches are briefly classified and the advantages and disadvantages of the various model approaches and methodologies are assessed.     

Dealing with uncertainty in the assessment of human exposure to radioactivity in food and the environment

This paper presents an overview of the approach used to assess radiation dose and risk to members of the public from radioactivity in food and the environment. It describes uncertainties in the process and suggests ways of dealing with them to improve the risk assessment process. It also explains how uncertainty in the assessed dose/risk can be communicated to non-expert audiences such as members of the public. The issues covered in this paper apply to risk assessment of any contaminant and not only radioactivity.     

210Po in the marine environment with emphasis on its behaviour within the biosphere

The distribution and behaviour of the natural-series alpha-emitter polonium-210 in the marine environment has been under study for many years primarily due to its enhanced bioaccumulation, its strong affinity for binding with certain internal tissues, and its importance as a contributor to the natural radiation dose received by marine biota as well as humans consuming seafoods. Results from studies spanning nearly 5 decades show that ²¹⁰Po concentrations in organisms vary widely among the different phylogenic groups as well as between the different tissues of a given species. Such variation results in ²¹⁰Po concentration factors ranging from approximately 10³ to over 10⁶ depending upon the organism or tissue considered. ²¹⁰Po/²¹⁰Pb ratios in marine species are generally greater than unity and tend to increase up the food chain indicating that ²¹⁰Po is preferentially taken up by organisms compared to its progenitor ²¹⁰Pb. The effective transfer of ²¹⁰Po up the food chain is primarily due to the high degree of assimilation of the radionuclide from ingested food and its subsequent strong retention in the organisms. In some cases this mechanism may lead to an apparent biomagnification of ²¹⁰Po at the higher trophic level. Various pelagic species release ²¹⁰Po and ²¹⁰Pb packaged in organic biodetrital particles that sink and remove these radionuclides from the upper water column, a biogeochemical process which, coupled with scavenging rates of this radionuclide pair, is being examined as a possible proxy for estimating downward organic carbon fluxes in the sea. Data related to preferential bioaccumulation in various organisms, their tissues, resultant radiation doses to these species, and the processes by which ²¹⁰Po is transferred and recycled through the food web are discussed. In addition, the main gaps in our present knowledge and proposed areas for future studies on the biogeochemical behaviour of ²¹⁰Po and its use as a tracer of oceanographic processes are highlighted in this review.     

Determination activity of radionuclides in marine sediment by gamma spectrometer with anti cosmic shielding

In this work, the activities of radionuclides in a marine sediment sample have been determined. The gamma spectrometer comprises an N type coaxial HPGe detector with active shielding to reduce cosmic background. The mass activities of radionuclides have been derived and found to be around a few Bq kg⁻¹ to several hundreds Bq kg⁻¹ with relative uncertainties in this paper quoted corresponding to the combined standard uncertainties (k = 1).     

Sources of anthropogenic radionuclides in the environment: a review

Studies of radionuclides in the environment have entered a new era with the renaissance of nuclear energy and associated fuel reprocessing, geological disposal of high-level nuclear wastes, and concerns about national security with respect to nuclear non-proliferation. This work presents an overview on sources of anthropogenic radionuclides in the environment, as well as a brief discussion of salient geochemical behavior of important radionuclides. We first discuss the following major anthropogenic sources and current developments that have lead, or could potentially contribute, to the radionuclide contamination of the environment: (1) nuclear weapons program; (2) nuclear weapons testing; (3) nuclear power plants; (4) uranium mining and milling; (5) commercial fuel reprocessing; (6) geological repository of high-level nuclear wastes that include radionuclides might be released in the future, and (7) nuclear accidents. Then, we briefly summarize the inventory of radionuclides ⁹⁹Tc and ¹²⁹I, as well as geochemical behavior for radionuclides ⁹⁹Tc, ¹²⁹I, and ²³⁷Np, because of their complex geochemical behavior, long half-lives, and presumably high mobility in the environment; biogeochemical cycling and environment risk assessment must take into account speciation of these redox-sensitive radionuclides.     

Development of a new aerosol monitoring system and its application in Fukushima nuclear accident related aerosol radioactivity measurement at the CTBT radionuclide station in Sidney of Canada

A high volume aerosol sampler ("Grey Owl") has been designed and developed at the Radiation Protection Bureau, Health Canada. Its design guidance is based on the need for a low operational cost and reliable sampler to provide daily aerosol monitoring samples that can be used as reference samples for radiological studies. It has been developed to provide a constant air flow rate at low pressure drops (∼3 kPa for a day sampling) with variations of less than ±1% of the full scale flow rate. Its energy consumption is only about 1.5 kW for a filter sampling over 22,000 standard cubic meter of air. It has been demonstrated in this Fukushima nuclear accident related aerosol radioactivity monitoring study at Sidney station, B.C. that the sampler is robust and reliable. The results provided by the new monitoring system have been used to support decision-making in Canada during an emergency response.     

Dose assessment for marine biota and humans from discharge of (131)I to the marine environment and uptake by algae in Sydney, Australia

Iodine-131 reaches the marine environment through its excretion to the sewer by nuclear medicine patients followed by discharge through coastal and deepwater outfalls. ¹³¹I has been detected in macroalgae, which bio-accumulate iodine, growing near the coastal outfall of Cronulla sewage treatment plant (STP) since 1995. During this study, ¹³¹I levels in liquid effluent and sludge from three Sydney STPs as well as in macroalgae (Ulva sp. and Ecklonia radiata) growing near their shoreline outfalls were measured. Concentration factors of 176 for Ulva sp. and 526 for E. radiata were derived. Radiation dose rates to marine biota from ¹³¹I discharged to coastal waters calculated using the ERICA dose assessment tool were below the ERICA screening level of 10 μGy/hr. Radiation dose rates to humans from immersion in seawater or consumption of Ulva sp. containing ¹³¹I were three and two orders of magnitude below the IAEA screening level of 10 μSv/year, respectively.     

Solid partitioning and solid-liquid distribution of Po and Pb in marine anoxic sediments: roads of Cherbourg at the northwestern France

A sequential extraction protocol has been used to determine the solid-phase partition of ²¹⁰Po and ²¹⁰Pb in anoxic marine sediment from the roads of Cherbourg (France) in the central English Channel. Measurements were also obtained in pore waters, in which ²¹⁰Po activities range between 1 and 20 mBq L⁻¹ and ²¹⁰Pb activities between 2.4 and 3.8 mBq L⁻¹, with highest activities in the topmost layer. These activities are higher than in seawater, suggesting that sediment act as a source of both ²¹⁰Po and ²¹⁰Pb for overlying water. The ²¹⁰Po profile in the pore waters is apparently correlated with those obtained for Fe, Mn and SO₄²⁻, suggesting an influence of early diagenetic processes on the ²¹⁰Po solid-liquid distribution. In the sediment, ²¹⁰Po is predominantly bound to organic matter or chromium reducible sulphides, and residuals (clay minerals and refractory oxides). Our results indicate that ²¹⁰Po is not significantly bound to AVS, i.e. acid volatile sulphides: bioturbation could play a role by the early redistribution of ²¹⁰Po bound to acid volatile sulphides in the sediment. ²¹⁰Po, ²¹⁰Pb and Pb exhibit differences in terms of distribution, probably due to a different mode of penetration in the sediment. This work provides information on solid and liquid distribution of ²¹⁰Po and ²¹⁰Pb in marine sediment. These data are very scarce in the litterature.