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.     

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.     

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.     

Natural and artificial radioactivity determination of some medicinal plants

Several medicinal plants used in Italy were analysed to determine natural and artificial radioactivity in those parts (leaves, fruits, seeds, roots, peduncles, flowers, barks, berries, thallus) used generally as remedies. The radionuclides were determined by alpha (²³⁸U, ²¹⁰Po) and gamma (²¹⁴Pb-Bi, ²¹⁰Pb, ⁴⁰K and ¹³⁷Cs) spectrometry. ²³⁸U ranged between <0.1 and 7.32 Bq kg_dry⁻¹; ²¹⁰Po between <0.1 and 30.3 Bq kg_dry⁻¹; ²¹⁴Pb-²¹⁴Bi between <0.3 and 16.6 Bq kg_dry⁻¹; ²¹⁰Pb between <3 and 58.3 Bq kg_dry⁻¹; ⁴⁰K between 66.2 and 3582.0 Bq kg_dry⁻¹; ¹³⁷Cs between <0.3 and 10.7 Bq kg_dry⁻¹. The percentage of ²¹⁰Po extraction in infusion and decoction was also determined; the arithmetical mean value of percentage of ²¹⁰Po extraction resulted 20.7 ± 7.5.     

Escaping radioactivity from coal-fired power plants (CPPs) due to coal burning and the associated hazards: a review

Coal, like most materials found in nature, contains trace quantities of the naturally occurring primordial radionuclides, i.e. of ⁴⁰K and of ²³⁸U, ²³²Th and their decay products. Therefore, the combustion of coal results in the released into the environment of some natural radioactivity (1.48 TBq y⁻¹), the major part of which (99 %) escapes as very fine particles, while the rest in fly ash. The activity concentrations of natural radionuclides measured in coals originated from coal mines in Greece varied from 117 to 435 Bq kg⁻¹ for ²³⁸U, from 44 to 255 Bq kg⁻¹ for ²²⁶Ra, from 59 to 205 Bq kg⁻¹ for ²¹⁰Pb, from 9 to 41 Bq kg⁻¹ for ²²⁸Ra (²³²Th) and from 59 to 227 Bq kg⁻¹ for ⁴⁰K. Fly ash escapes from the stacks of coal-fired power plants in a percentage of 3-1% of the total fly ash, in the better case. The natural radionuclide concentrations measured in fly ash produced and retained or escaped from coal-fired power plants in Greece varied from 263 to 950 Bq kg⁻¹ for ²³⁸U, from 142 to 605 Bq kg⁻¹ for ²²⁶Ra, from 133 to 428 Bq kg⁻¹ for ²¹⁰Pb, from 27 to 68 Bq kg⁻¹ for ²²⁸Ra (²³²Th) and from 204 to 382 Bq kg⁻¹ for ⁴⁰K. About 5% of the total ash produced in the coal-fired power plants is used as substitute of cement in concrete for the construction of dwellings, and may affect indoor radiation doses from external irradiation and the inhalation of radon decay products (internal irradiation) is the most significant. The resulting normalized collective effective doses were 6 and 0.5 man-Sv (GW a)⁻¹ for typical old and modern coal-fired power plants, respectively.     

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.     

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.     

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.     

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.     

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.     

Natural radioactivity levels in topsoil from the Pearl River Delta Zone, Guangdong, China

Concentrations of the natural radionuclides ²³⁸U, ²²⁶Ra, ²³²Th and ⁴⁰K have been measured by γ-ray spectrometry in 796 topsoil samples from the Pearl River Delta Zone (PRDZ) of Guangdong, China. The mean concentrations for ²³⁸U, ²²⁶Ra, ²³²Th and ⁴⁰K were found to be 140 ± 37 Bq kg⁻¹, 134 ± 41 Bq kg⁻¹, 187 ± 80 Bq kg⁻¹ and 680 ± 203 Bq kg⁻¹ dry mass, respectively. These values were all higher than the mean values in soil for China and the world. Outdoor air-absorbed dose rates, calculated from activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K, ranged from 86 to 237 nGy h⁻¹, with a mean value of 165 ± 46 nGy h⁻¹. The corresponding annual outdoor effective dose rate per person was estimated to be between 0.11 and 0.29 mSv y⁻¹, with a mean value of 0.20 ± 0.06 mSv y⁻¹, which was also higher than the world mean value of 0.07 mSv y⁻¹. The radium equivalent activity (Ra_eq) and the external hazard index (I_r) resulted from the natural radionuclides in soil, were also calculated and found to vary from 230 to 676 Bq kg⁻¹ and from 0.6 to 1.8, respectively. The Ra_eq and the I_r in all the investigated regions were up to 75% higher than the set limits of 370 Bq kg⁻¹ and 1.0, respectively.     

Comparative study of natural radioactivity levels in soil samples from the Upper Siwaliks and Punjab,India using gamma-ray spectrometry

Natural radioactive materials under certain conditions can reach hazardous radiological levels. So, it becomes necessary to study the natural radioactivity levels in soil to assess the dose for the population in order to know the health risks and to have a baseline for future changes in the environmental radioactivity due to human activities. The natural radionuclide (²²⁶Ra, ²³²Th, and ⁴⁰K) contents in soil were determined for 26 locations around the Upper Siwaliks of Kala Amb, Nahan and Morni Hills, Northern India, using high-resolution gamma-ray spectrometric analysis. It was observed that the concentration of natural radionuclides viz., ²²⁶Ra, ²³²Th and ⁴⁰K, in the soil varies from 28.3 ± 0.5 to 81.0 ± 1.7 Bq kg⁻¹, 61.2 ± 1.3 to 140.3 ± 2.6 Bq kg⁻¹ and 363.4 ± 4.9 to 1002.2 ± 11.2 Bq kg⁻¹ respectively. The total absorbed dose rate calculated from activity concentration of ²²⁶Ra, ²³²Th and ⁴⁰K ranged from 71.1 to 162.0 nGy h⁻¹. The radium equivalent (R_eq) and the external hazard index (H_ex), which resulted from the natural radionuclides in soil, were also calculated and found to vary from 149.4 to 351.8 Bq kg⁻¹and from 0.40 to 0.95 respectively. These values in Upper Siwaliks area were compared with that from the adjoining areas of Punjab. The radium equivalent activities in all the soil samples were lower than the limit (370 Bq kg⁻¹) set in the Organization for Economic Cooperation and Development (OECD) report and the dose equivalent was within the safe limit of 1 mSv y⁻¹.     

Ra–Po–Pb isotope systematics in waters of Sambhar Salt Lake,Rajasthan (India): geochemical characterization and particulate reactivity

The Sambhar Salt Lake hydrological system, including river waters, groundwaters, evaporating pans and sub-surface brines, has been analyzed for the salt content (TDS) and naturally occurring radionuclides (²¹⁰Po, ²¹⁰Pb and ^226,228Ra). The abundance of these radionuclides and their activity ratios show a wide variation in different hydrological regimes, which helps to geochemically characterize the lake system. A significantly lower Ra to total dissolved solids (TDS) ratio in the brines (by two to three orders of magnitude), when compared to the groundwaters and river waters, suggests removal of dissolved Ra by co-precipitation with Ca–Mg minerals at an early stage of the brine evolution. The concentration of Ra in evaporating lake/pan waters saturates at a value of about 35 Bq L⁻¹ over the salinity range of 100–370 g L⁻¹; attributable to its equilibration with the clay minerals. The two distinct regimes, saline lake system (lake water, evaporating pans and sub-surface brines) and groundwaters have been identified based on their differences in the distribution of ^226,228Ra isotopes. This observation points to the conclusion that the groundwaters and the lake brines are not intimately coupled in terms of their origin and evolution. The abundances of ²¹⁰Po and ²¹⁰Pb along with their activity ratios (²¹⁰Po/²¹⁰Pb) are markedly different among the surface lake waters/evaporating pans, sub-surface lake brines and groundwaters. These differences are explained in terms of different geochemical behaviour of these nuclides in presence of algae and organic matter present in these water regimes.     

Concentrations of U,U, U,Th, Th,Th, Ra,Ra, Ra,Po, Pb and Pb in drinking water in Italy: reconciling safety standards based on measurements of gross α and β

Some important naturally occurring α- and β-radionuclides in drinking water samples collected in Italy were determined and the radiological quality evaluated. The mean activity concentrations (mBq L⁻¹) of the radionuclides in the water samples were almost in the order: 26 ± 36 (²³⁴U) > 21 ± 30 (²³⁸U) > 8.9 ± 15 (²²⁶Ra) > 4.8 ± 6.3 (²²⁸Ra) > 4.0 ± 4.1 (²¹⁰Pb) > 3.2 ± 3.7 (²¹⁰Po) > 2.7 ± 1.2 (²¹²Pb) > 1.4 ± 1.8 (²²⁴Ra) > 1.1 ± 1.3 (²³⁵U) > 0.26 ± 0.39 (²²⁸Th) > 0.0023 ± 0.0009 (²³⁰Th) > 0.0013 ± 0.0006 (²³²Th). The mean estimated dose (μSv yr⁻¹) to an adult from the water intake was in this order: 2.8 ± 3.3 (²¹⁰Po) > 2.4 ± 3.2 (²²⁸Ra) > 2.1 ± 2.1 (²¹⁰Pb) > 1.8 ± 3.1 (²²⁶Ra) > 0.94 ± 1.30 (²³⁴U) > 0.70 ± 0.98 (²³⁸U) > 0.069 ± 0.087 (²²⁴Ra) > 0.036 ± 0.044 (²³⁵U) > 0.014 ± 0.021 (²²⁸Th) > 0.012 ± 0.005 (²¹²Pb) > 0.00035 ± 0.00029 (²³⁰Th) > 0.00022 ± 0.00009 (²³²Th). It is obvious that ²¹⁰Po, ²²⁸Ra, ²¹⁰Pb and ²²⁶Ra are the most important dose contributors in the drinking water intake. As far as the seventeen brands of analysed drinking water were concerned, the committed effective doses were in the range of 2.81–38.5 μSv yr⁻¹, all well below the reference level of the committed effective dose (100 μSv yr⁻¹) recommended by the WHO. These data throw some light on the scale of the radiological impact on the public from some naturally occurring radionuclides in drinking water, and can also serve as a comparison for the dose contribution from artificial radionuclides released to the environment as a result of human practices. Based on the radionuclide composition in the analysed waters, comment was made on the new screening level for gross α activity in guidelines for drinking-water quality recommended by the WHO, 2004.     

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.     

Recent atmospheric lead deposition recorded in an ombrotrophic peat bog of Great Hinggan Mountains, Northeast China, from Pb and Cs dating

Radioactive markers are useful in dating lead deposition patterns from industrialization in peat archive. Peat cores were collected in an ombrotrophic peat bog in the Great Hinggan Mountains in Northeast China in September 2008 and dated using ²¹⁰Pb and ¹³⁷Cs radiometric techniques. The mosses in both cores were examined systematically for dry bulk density, water and ash content. Lead also was measured using atomic emission spectroscopy with inductively coupled plasma (ICP-AES). Both patterned peat profiles were preserved well without evident anthropogenic disturbance. Unsupported ²¹⁰Pb and ¹³⁷Cs decreased with the depth in both of the two sample cores. The ²¹⁰Pb chronologies were established using the constant rate of supply model (CRS) and are in good agreement with the ¹³⁷Cs time marker. Recent atmospheric ²¹⁰Pb flux in Great Hinggan Mountains peat bog was estimated to be 337 Bq m⁻² y⁻¹, which is consistent with published data for the region. Lead deposition rate in this region was also derived from these two peat cores and ranged from 24.6 to 55.8 mg m⁻² y⁻¹ with a range of Pb concentration of 14-262 μg g⁻¹. The Pb deposition patterns were consistent with increasing industrialization over the last 135-170 y, with a peak of production and coal burning in the last 50 y in Northeast China. This work presents a first estimation of atmospheric Pb deposition rate in peatlands in China and suggests an increasing trend of environmental pollution due to anthropogenic contaminants in the atmosphere. More attention should be paid to current local pollution problems, and society should take actions to seek a balance between economic development and environmental protection.     

The effect of air mass origin on the ambient concentrations of Be and Pb in Islamabad, Pakistan

Concentration of radionuclides ²¹⁰Pb and ⁷Be, having half lives of 22.3 years and 53.29 days, respectively, in the surface air samples of Islamabad (33.38° N, 73.10° E and Altitude ∼536 m asl.) are measured. The non-destructive technique of gamma-spectrometry, with a high purity germanium HPGe detector, was employed for the analysis of all samples. The annual average concentrations of ²¹⁰Pb and ⁷Be in the surface air samples were determined as 0.284 ± 0.15 and 3.171 ± 1.14 mBq m⁻³, respectively. Our results have shown a seasonal variation of the concentration of ⁷Be in air samples with high values for the spring season. High concentrations for ²¹⁰Pb are obtained when air masses originate from plain areas of Pothohar region, located in the South-West, West and North West of Islamabad. Our values of concentrations show a nice agreement with the relevant reported results.     

Radiological monitoring: terrestrial natural radionuclides in Kinta District,Perak, Malaysia

Natural background gamma radiation and radioactivity concentrations were investigated from 2003 to 2005 in Kinta District, Perak, Malaysia. Sample locations were distant from any ‘amang’ processing plants. The external gamma dose rates ranged from 39 to 1039 nGy h⁻¹. The mean external gamma dose rate was 222 ± 191 nGy h⁻¹. Small areas of relatively enhanced activity were located having external gamma dose rates of up to 1039 ± 104 nGy h⁻¹. The activity concentrations of ²³⁸U, ²³²Th and ⁴⁰K were analyzed by using a high-resolution co-axial HPGe detector system. The activity concentration ranges were 12–426 Bq kg⁻¹ for ²³⁸U, 19–1377 Bq kg⁻¹ for ²³²Th and <19–2204 Bq kg⁻¹ for ⁴⁰ K. Based on the radioactivity levels determined, the gamma-absorbed dose rates in air at 1 m above the ground were calculated. The calculated dose rates and measured dose rates had a good correlation coefficient, R of 0.94. To evaluate the radiological hazard of the natural radioactivity, the radium equivalent activity, the gamma-absorbed dose rate and the mean population weighted dose rate were calculated. An isodose map for the Kinta District was also produced.     

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.