Aspects on the analysis of 210Po

There has been little development regarding analysis of polonium (Po) in environmental samples since the 1960ies. This is due to the straightforward spontaneous deposition of this element on silver (Ag), nickel (Ni) or copper (Cu) without any radiochemical separation. For many years, no radiochemical yield determinant was used and it was generally supposed that the yield was 100% after two depositions. Counting was often done using ZnS scintillation counter coupled to a photomultiplier tube. However, the use of the yield determinants ²⁰⁸Po and ²⁰⁹Po and the development of alpha spectrometry showed that the yield was lower. Furthermore, the tendency of Po to volatilize at low temperatures constrains the sample preparation techniques; dry-ashing cannot be used. But during the wet-ashing procedure, there are still some losses.The aim of this study was to evaluate the Po losses during wet-ashing by the use of a double-tracer technique. We have found that the losses were about 30% when open glass beakers were used and about 17% when the samples were digested in microwave oven. When long-necked bottles (Kjeldahl flasks) were used, a loss of about 20% was registered.It has also been observed that ²¹⁰Pb to some extent is plating out together with its daughter nuclide Po during the electrochemical deposition. This will result in a systematic error since an unknown amount of supported ²¹⁰Po will be produced from the ²¹⁰Pb decay depending on the fraction of ²¹⁰Pb being deposited on the disc and the waiting time between deposition and measurement of the sample. A further consequence of this is that in the assessment of the ²¹⁰Pb content in the sample, very often the remaining liquid is stored after deposition for build-up of ²¹⁰Po. Since some ²¹⁰Pb is lost on the disc, the result for ²¹⁰Pb will be too low. Both these systematic errors give rise to a too high ²¹⁰Po/²¹⁰Pb ratio. The fraction of ²¹⁰Pb which is plating out has been assessed in this study for different matrices and is about 50-90%. During the measurement by solid state Si-detectors, some Po is evaporated in the vacuum conditions contaminating the detectors. Experiments have here been done by heating the discs after deposition which indicate that less Po is evaporated from Ag than from Ni. The losses from Ag are less than that from the other metals probably due to a deeper penetration into the surface of Po. We conclude that in most aspects, Ag is better to use than the other plating metals.     

Study of 210Po and 210Pb in the riverine environments of coastal Karnataka

Activity of ²¹⁰Po and ²¹⁰Pb were measured in soil and sediment samples collected from the major rivers Kali, Sharavathi and Netravathi of Coastal Karnataka. The activity of these two radionuclides were determined by radiochemical separation of ²¹⁰Po and counting the activity using a ZnS(Ag) Alpha counter. The activity of ²¹⁰Pb was higher than that of ²¹⁰Po in the riverine environs. The ²¹⁰Po and ²¹⁰Pb content in sediment was found to increase with silt/clay and organic matter contents. However no significant correlation was found between the activity ²¹⁰Po and ²¹⁰Pb with pH in sediments. The activity of ²¹⁰Po and ²¹⁰Pb and influence of physico-chemical parameters on these radionuclides were studied and discussed in this paper.     

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.     

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.     

210Pb and 210Po in Finnish cereals

A survey was carried out on the activity concentrations of ²¹⁰Pb and ²¹⁰Po in cereal grains produced in Finland. The cereal species were wheat (Triticum aestivum), rye (Secale cereale), oats (Avena sativa) and barley (Hordeum vulgare), which account for 90% of the Finnish consumption of cereal products. The survey consisted of 18 flour and 13 unprocessed cereal samples and one hulled grain sample from 22 flour mills. According to the results, the mean ²¹⁰Pb/²¹⁰Po concentrations in wheat grains, wheat flour, rye flour, oat grains and barley grains were 0.29, 0.12, 0.29, 0.36 and 0.36 Bq kg⁻¹, respectively. Combined with the consumption rates of the products, we assess that the mean effective doses from ²¹⁰Pb and ²¹⁰Po in cereal products for the adult male and female population are 22 and 17 μSv per year, respectively.     

Accumulation of 210Po in Baltic invertebrates

This paper presents the results of an investigation of the ²¹⁰Po contents of Baltic marine invertebrates. The ²¹⁰Po concentrations fall within the range 11·3–78·9 Bq kg⁻¹ (dry wt), the higher values relating to polychaeta, priapulida and malacostraca and the lower levels to bivalvia. It is demonstrated that ¹⁰Po is non-uniformly distributed within the isopod Mesidotea entomon and the bivalve Mya arenaria. The ²¹⁰Po contents of the internal organs decreasing in the order-hepatopancreas > alimentary tract > gill > muscle. Moreover, the results indicate the dominant role of the digestive organs of these invertebrates in controlling absorption and elimination of ²¹⁰Po.     

Polonium-210 and lead-210 in the terrestrial environment: a historical review

The radionuclides ²¹⁰Po and ²¹⁰Pb widely present in the terrestrial environment are the final long-lived radionuclides in the decay of ²³⁸U in the earth’s crust. Their presence in the atmosphere is due to the decay of ²²²Rn diffusing from the ground. The range of activity concentrations in ground level air for ²¹⁰Po is 0.03-0.3 Bq m⁻³ and for ²¹⁰Pb 0.2-1.5 Bq m⁻³.In drinking water from private wells the activity concentration of ²¹⁰Po is in the order of 7-48 mBq l⁻¹ and for ²¹⁰Pb around 11-40 mBq l⁻¹. From water works, however, the activity concentration for both ²¹⁰Po and ²¹⁰Pb is only in the order of 3 mBq l⁻¹.Mosses, lichens and peat have a high efficiency in capturing ²¹⁰Po and ²¹⁰Pb from atmospheric fallout and exhibit an inventory of both ²¹⁰Po and ²¹⁰Pb in the order of 0.5-5 kBq m⁻² in mosses and in lichens around 0.6 kBq m⁻². The activity concentrations in lichens lies around 250 Bq kg⁻¹, dry mass.Reindeer and caribou graze lichen which results in an activity concentration of ²¹⁰Po and ²¹⁰Pb of about 1-15 Bq kg⁻¹ in meat from these animals. The food chain lichen-reindeer or caribou, and Man constitutes a unique model for studying the uptake and retention of ²¹⁰Po and ²¹⁰Pb in humans. The effective annual dose due to ²¹⁰Po and ²¹⁰Pb in people with high consumption of reindeer/caribou meat is estimated to be around 260 and 132 μSv a⁻¹ respectively.In soils, ²¹⁰Po is adsorbed to clay and organic colloids and the activity concentration varies with soil type and also correlates with the amount of atmospheric precipitation. The average activity concentration levels of ²¹⁰Po in various soils are in the range of 20-240 Bq kg⁻¹.Plants become contaminated with radioactive nuclides both by absorption from the soil (supported Po) and by deposition of radioactive fallout on the plants directly (unsupported Po). In fresh leafy plants the level of ²¹⁰Po is particularly high as the result of the direct deposition of ²²²Rn daughters from atmospheric deposition. Tobacco is a terrestrial product with high activity concentrations of ²¹⁰Po and ²¹⁰Pb. The overall average activity concentration of ²¹⁰Po is 13 ± 2 Bq kg⁻¹. It is rather constant over time and by geographical origin.The average median daily dietary intakes of ²¹⁰Po and ²¹⁰Pb for the adult world population was estimated to 160 mBq day⁻¹ and 110 mBq day⁻¹, corresponding to annual effective doses of 70 μSv a⁻¹ and 28 μSv a⁻¹, respectively. The dietary intakes of ²¹⁰Po and ²¹⁰Pb from vegetarian food was estimated to only 70 mBq day⁻¹ and 40 mBq day⁻¹ corresponding to annual effective doses of 30.6 μSv a⁻¹ and 10 μSv a⁻¹, respectively. Since the activity concentration of ²¹⁰Po and ²¹⁰Pb in seafood is significantly higher than in vegetarian food the effective dose to populations consuming a lot of seafood might be 5-15 fold higher.     

The sources and fate of 210Po in the urban air: A review

The origin of ²¹⁰Po activity and its fluctuations in the air are discussed in this paper. In the case of atmospheric aerosol samples, a comparison of the ²¹⁰Po/²¹⁰Pb and ²¹⁰Bi/²¹⁰Pb activity ratios makes it possible not only to determine aerosol residence times but also to appraise the contribution of the unsupported ²¹⁰Po coming from other sources than ²²²Rn decay, such as human industrial activities, especially coal combustion. A simple mathematical method makes it possible to observe the seasonal fluctuations of the anthropogenic excess of ²¹⁰Po in the urban air. The average doses of ²¹⁰Po intake with food (including drinking water) and inhalation of urban aerosols are usually lower than those from ²¹⁰Po intake by cigarette smokers and negligible in comparison to total natural radiation exposure.     

Biomonitoring of ²¹⁰Po and ²¹⁰Pb using lichens and mosses around coal-fired power plants in Western Turkey

Mosses and lichens are useful biological indicators of environmental contamination for a variety of metals and radionuclides of both natural and artificial origin. These plants lack a well-developed root system and rely largely on atmospheric deposition for nourishment. Therefore in the study, different lichens (Cladonia convoluta, Cladonia foliacea) and mosses (Homalothecium sericeum, Hypnum lacunosum, Hypnum cupressiforme, Tortella tortuosa, Didymodon acutus, Syntrichia ruralis, Syntrichia intermedia, Pterogonium graciale, Isothecium alopecuroides, Pleurochatae squarrosa) were collected around the Yata?an (Mu?la), Soma (Manisa), Seyitömer - Tunçbilek (Kütahya) coal-fired power plants and investigated for potential use as biomonitors for ²¹⁰Po and ²¹⁰Pb deposition. While the activity concentrations of ²¹⁰Po and ²¹⁰Pb in lichens are in the ranges of 151 ± 7-593 ± 21 and 97 ± 5-364 ± 13 Bq kg⁻¹, for mosses the ranges for ²¹⁰Po and ²¹⁰Pb are 124 ± 5-1125 ± 38 and 113 ± 4-490 ± 17 Bq kg⁻¹, respectively. In the study, the moss samples were observed to accumulate more ²¹⁰Po and ²¹⁰Pb compared to lichens. While the most suitable biomonitor was a moss species (H. lacunosum) for Yata?an (Mu?la), it was another moss species (S. intermedia) for Soma (Manisa) and Seyitömer - Tunçbilek (Kütahya) sites. ²¹⁰Po concentrations were found higher than ²¹⁰Pb concentrations at the all sampling stations.     

Po-210 and Pb-210 as atmospheric tracers and global atmospheric Pb-210 fallout: a review

Over the past ∼5 decades, the distribution of ²²²Rn and its progenies (mainly ²¹⁰Pb, ²¹⁰Bi and ²¹⁰Po) have provided a wealth of information as tracers to quantify several atmospheric processes that include: i) source tracking and transport time scales of air masses; ii) the stability and vertical movement of air masses iii) removal rate constants and residence times of aerosols; iv) chemical behavior of analog species; and v) washout ratios and deposition velocities of aerosols. Most of these applications require that the sources and sink terms of these nuclides are well characterized.Utility of ²¹⁰Pb, ²¹⁰Bi and ²¹⁰Po as atmospheric tracers requires that data on the ²²²Rn emanation rates is well documented. Due to low concentrations of ²²⁶Ra in surface waters, the ²²²Rn emanation rates from the continent is about two orders of magnitude higher than that of the ocean. This has led to distinctly higher ²¹⁰Pb concentrations in continental air masses compared to oceanic air masses. The highly varying concentrations of ²¹⁰Pb in air as well the depositional fluxes have yielded insight on the sources and transit times of aerosols. In an ideal enclosed air mass (closed system with respect to these nuclides), the residence times of aerosols obtained from the activity ratios of ²¹⁰Pb/²²²Rn, ²¹⁰Bi/²¹⁰Pb, and ²¹⁰Po/²¹⁰Pb are expected to agree with each other, but a large number of studies have indicated discordance between the residence times obtained from these three pairs. Recent results from the distribution of these nuclides in size-fractionated aerosols appear to yield consistent residence time in smaller-size aerosols, possibly suggesting that larger size aerosols are derived from resuspended dust. The residence times calculated from the ²¹⁰Pb/²²²Rn, ²¹⁰Bi/²¹⁰Pb, and ²¹⁰Po/²¹⁰Pb activity ratios published from 1970’s are compared to those data obtained in size-fractionated aerosols in this decade and possible reasons for the discordance is discussed with some key recommendations for future studies.The existing global atmospheric inventory data of ²¹⁰Pb is re-evaluated and a ‘global curve’ for the depositional fluxes of ²¹⁰Pb is established. A current global budget for atmospheric ²¹⁰Po and ²¹⁰Pb is also established. The relative importance of dry fallout of ²¹⁰Po and ²¹⁰Pb at different latitudes is evaluated. The global values for the deposition velocities of aerosols using ²¹⁰Po and ²¹⁰Pb are synthesized.     

Increase of 210Po levels in human semen fluid after mussel ingestion

Polonium-210 (²¹⁰Po) radioactive concentrations were determined in human semen fluid of vasectomized non-smoker volunteers. The ²¹⁰Po levels ranged from 0.10 to 0.39 mBq g⁻¹ (mean: 0.23 ± 0.08 mBq g⁻¹). This value decreased to 0.10 ± 0.02 mBq g⁻¹ (range from 0.07 to 0.13 mBq g⁻¹) after two weeks of a controlled diet, excluding fish and seafood. Then, volunteers ate during a single meal 200 g of the cooked mussel Perna perna L., and ²¹⁰Po levels were determined again, during ten days, in semen fluid samples collected every morning. Volunteers continued with the controlled diet and maintained sexual abstinence through the period of the experiment. A 300% increase of ²¹⁰Po level was observed the day following mussel consumption, with a later reduction, such that the level returned to near baseline by day 4.     

Radionuclides in marine mammals off the Portuguese coast

Radionuclide analyses were performed in tissue samples including muscle, gonad, liver, mammary gland, and bone of marine mammals stranded on the Portuguese west coast during January-July 2006. Tissues were collected from seven dolphins (Delphinus delphis and Stenella coeruleoalba) and one pilot whale (Globicephala sp.). Samples were analyzed for ²¹⁰Po and ²¹⁰Pb by alpha spectrometry and for ¹³⁷Cs and ⁴⁰K by gamma spectrometry. Po-210 concentrations in common dolphin’s muscle (D. delphis) averaged 56 ± 32 Bq kg⁻¹ wet weight (w.w.), while ²¹⁰Pb averaged 0.17 ± 0.07 Bq kg⁻¹ w.w., ¹³⁷Cs averaged 0.29 ± 0.28 Bq kg⁻¹ w.w., and ⁴⁰K 129 ± 48 Bq kg⁻¹ w.w. Absorbed radiation doses due to these radionuclides for the internal organs of common dolphins were computed and attained a 1.50 μGy h⁻¹ on a whole body basis. ²¹⁰Po was the main contributor to the weighted absorbed dose, accounting for 97% of the dose from internally accumulated radionuclides. These computed radiation doses in dolphins are compared to radiation doses from ²¹⁰Po and other radionuclides reported for human tissues. Due to the high ²¹⁰Po activity concentration in dolphins, the internal radiation dose in these marine mammals is about three orders of magnitude higher than in man.     

Assessment of Po and Pb in marine biota of the Mallipattinam ecosystem of Tamil Nadu, India

To provide baseline data on background radiation levels for the future assessment of the impact of nuclear and thermal power stations, a systematic study was carried out in the Mallipattinam ecosystem of Tamil Nadu, India. Mallipattinam is located between the Kudankulam and Kalpakkam nuclear power plants and near to Tuticorin thermal power plant. Water, sediments, seaweeds, crustaceans, molluscs, and fish were collected to measure the concentrations of ²¹⁰Po and ²¹⁰Pb. The concentrations of ²¹⁰Po and ²¹⁰Pb in most samples are comparable to values reported worldwide. In fish, the concentrations of ²¹⁰Po and ²¹⁰Pb are in the range 16-190 Bq kg⁻¹ and 8-153 Bq kg⁻¹, respectively. The concentration factors of ²¹⁰Po and ²¹⁰Pb for the biotic components ranges from 10³ to 10⁶.     

Activities of Po and Pb in the water column at Kuala Selangor, Malaysia

Natural radionuclides, such as ²¹⁰Po and ²¹⁰Pb were measured in the water samples collected from six stations at Kuala Selangor, Malaysia. Results for ²¹⁰Po and ²¹⁰Pb in dissolved and particulate phases have showed the difference in distribution and chemical behavior. The fluctuation activities of ²¹⁰Po and ²¹⁰Pb depend on wave action, geology and degree of fresh water input occurring at study areas and probably due to different sampling dates. The distribution coefficient, K_d, values of ²¹⁰Po and ²¹⁰Pb ranged from 2.0 × 10³ l g⁻¹ to 265.15 × 10⁵ l g⁻¹, and from 3.0 × 10³ l g⁻¹ to 558.16 × 10⁵ l g⁻¹, respectively. High K_d values of ²¹⁰Po and ²¹⁰Pb indicated that a strong adsorption of ²¹⁰Po and ²¹⁰Pb onto suspended particles, and the sinking of both nuclides on the seabed at study locations were controlled by the characteristics of suspended particles.     

Accumulation of 210Po in selected species of Baltic fish

Results are presented here for the ²¹⁰Po contents of selected species of Baltic fish. It is shown that ²¹⁰Po is non-uniformly distributed within these fish, the highest levels being found in the digestive organs, particularly within the intestine. It is found that the proportional contribution by the digestive organs to the total accumulation of ²¹⁰Po is correlated with the degree of repletion of the stomach and that this decreases if food is lacking. Moreover, it is observed that fish represent an important source of supply of ²¹⁰Po to humans.     

Levels and transfer of Po and Pb in Nordic terrestrial ecosystems

Recent developments regarding environmental impact assessment methodologies for radioactivity have precipitated the need for information on levels of naturally occurring radionuclides within and transfer to wild flora and fauna. The objectives of this study were therefore to determine activity concentrations of the main dose forming radionuclides ²¹⁰Po and ²¹⁰Pb in biota from terrestrial ecosystems thus providing insight into the behaviour of these radioisotopes. Samples of soil, plants and animals were collected at Dovrefjell, Central Norway and Olkiluoto, Finland. Soil profiles from Dovrefjell exhibited an approximately exponential fall in ²¹⁰Pb activity concentrations from elevated levels in humus/surface soils to “supported” levels at depth. Activity concentrations of ²¹⁰Po in fauna (invertebrates, mammals, birds) ranged between 2 and 123 Bq kg⁻¹ d.w. and in plants and lichens between 20 and 138 Bq kg⁻¹ d.w. The results showed that soil humus is an important reservoir for ²¹⁰Po and ²¹⁰Pb and that fauna in close contact with this media may also exhibit elevated levels of ²¹⁰Po. Concentration ratios appear to have limited applicability with regards to prediction of activity concentrations of ²¹⁰Po in invertebrates and vertebrates. Biokinetic models may provide a tool to explore in a more mechanistic way the behaviour of ²¹⁰Po in this system.     

Direct comparison of 210Po, 234Th and POC particle-size distributions and export fluxes at the Bermuda Atlantic Time-series Study (BATS) site

Particle-reactive, naturally occurring radionuclides are useful tracers of the sinking flux of organic matter from the surface to the deep ocean. Since the Joint Global Ocean Flux Study (JGOFS) began in 1987, the disequilibrium between ²³⁴Th and its parent ²³⁸U has become widely used as a technique to measure particle export fluxes from surface ocean waters. Another radionuclide pair, ²¹⁰Po and ²¹⁰Pb, can be used for the same purpose but has not been as widely adopted due to difficulty with accurately constraining the ²¹⁰Po/²¹⁰Pb radiochemical balance in the ocean and because of the more time-consuming radiochemical procedures. Direct comparison of particle flux estimated in different ocean regions using these short-lived radionuclides is important in evaluating their utility and accuracy as tracers of particle flux. In this paper, we present paired ²³⁴Th/²³⁸U and ²¹⁰Po/²¹⁰Pb data from oligotrophic surface waters of the subtropical Northwest Atlantic and discuss their advantages and limitations. Vertical profiles of total and particle size-fractionated ²¹⁰Po and ²³⁴Th activities, together with particulate organic carbon (POC) concentrations, were measured during three seasons at the Bermuda Atlantic Time-series Study (BATS) site. Both ²¹⁰Po and ²³⁴Th reasonably predict sinking POC flux caught in sediment traps, and each tracer provides unique information about the magnitude and efficiency of the ocean's biological pump.     

Polonium-210 in mussels and its implications for environmental alpha-autoradiography

Alpha-autoradiographic and radiochemical studies of the distributions of transuranic nuclides in the tissues and organs of mussels collected from the vicinity of the British Nuclear Fuels plc reprocessing plant at Sellafield, Cumbria, England, appeared to require assessment also of baseline alpha-activities of natural ²¹⁰ Po levels. Results for the latter were found to be in excess of the anthropogenic activities of Pu and Am isotopes. To ensure that the levels of ²¹⁰ Po in Cumbrian mussels were not artificially enhanced by local discharges and in the absence of published data, mussels from remote British and French coastal sites were also analyzed. General similarities in ²¹⁰Po concentrations (111 to 459 Bq kg⁻¹ dry) found in mussels soft parts suggest that the ²¹⁰Po levels in the Ravenglass mussels (279 Bq kg⁻¹) are natural and largely unsupported by ²¹⁰Pb; however these levels are as much as four times greater than the present day ^239+240Pu concentrations in the same samples. As the transuranic nuclide content of Cumbrian mussels produces a major component of the local critical group radiation exposure from the Sellafield discharges, this finding places in some perspective the significance of the baseline natural radionuclide concentrations in generating total exposure of the public. More specifically, these findings severely limit the usefulness of alpha-autoradiographic studies for transuranic nuclides performed on such samples. Because of the recently lower concentrations of alpha-emitting transuranic nuclides (mainly ²³⁸Pu, ^239+240Pu and ²⁴¹Am) in the Ravenglass environment, natural ²¹⁰Po is now a major contributor to alpha-track distributions in autoradiographic studies.     

Polonium (210Po) and lead (210Pb) in marine organisms and their transfer in marine food chains

The determination of ²¹⁰Po and ²¹⁰Pb was performed in marine organisms from the seashore to abyssal depths, encompassing a plethora of species from the microscopic plankton to the sperm whale. Concentrations of those radionuclides ranged from low values of about 5 × 10⁻¹ Bq kg⁻¹ (wet wt.) in jellyfish, to very high values of about of 3 × 10⁴ Bq kg⁻¹ (wet wt.) in the gut walls of sardines, with a common pattern of ²¹⁰Po > ²¹⁰Pb.These radionuclides are primarily absorbed from water and concentrated by phyto- and microzooplankton, and then are transferred to the next trophic level along marine food chains. Investigation in epipelagic, mesopelagic, bathypelagic and abyssobenthic organisms revealed that ²¹⁰Po is transferred in the marine food webs with transfer factors ranging from 0.1 to 0.7, and numerically similar to those of the energy transfer in the marine food chains. As ²¹⁰Po preferentially binds to amino acids and proteins, its transfer in food chains likely traces protein transfer and, thus, ²¹⁰Po transfer factors are similar to ecotrophic coefficients. ²¹⁰Pb is transferred less efficiently in marine food chains and this contributes to increased ²¹⁰Po:²¹⁰Pb activity ratios in some trophic levels.     

Transfer factors of Polonium from soil to parsley and mint

Transfer factors of ²¹⁰Po from soil to parsley and mint have been determined. Artificial polonium isotope (²⁰⁸Po) was used as a tracer to determine transfer factor of Po from soil to plant in pot experiments. Two plant growing systems were used for this study namely, an outdoor system and a sheltered system by a polyethylene tent. ²⁰⁸Po and ²¹⁰Po were determined in soil and different parts of the studied plants (stem and leaf), using alpha spectroscopy. The results have shown that there was a clear uptake of ²⁰⁸Po by roots to leaves and stems of both plants. Higher values of transfer factors using the ²¹⁰Po activity concentrations than the ²⁰⁸Po activity concentration were observed. Transfer factors of ²¹⁰Po from soil to parsley varied between 20 × 10⁻² and 50 × 10⁻² and 22 × 10⁻³ and 67 × 10⁻³ in mint, while ²⁰⁸Po transfer factors varied between 4 × 10⁻² and 12 × 10⁻² for parsley and 10 × 10⁻² and 22 × 10⁻² in mint. Transfer factors of Po were higher in those plants grown in the sheltered system than in the open system; about 75% of Po was transferred from atmosphere to parsley parts using the two systems. Ratios of transferred Po from soil to mint stem and leaf in the sheltered system were higher by 2 times from those in the open system.