Long term investigation of 137Cs in chicken meat and eggs from northwest Croatia.

This paper presents the results of long-term investigations of 137Cs activity concentrations in chicken meat and eggs from northwest Croatia for the period 1987-2018. The research has been done as a part of monitoring program of radioactive contamination in Croatia. The highest activity concentrations in both of these foodstuffs were measured in 1987 and have been decreasing exponentially ever since. The Fukushima-Daiichi accident in 2011 did not cause any increase of 137Cs activity concentrations. The ecological half-life for 137Cs was estimated to be 8.0 and 8.4 years for chicken meat and eggs respectively. The correlation between 137Cs in fallout and chicken meat as well as between 137Cs in fallout and eggs is very good, the respective correlation coefficients being 0.79 and 0.72, indicating that fallout was the main source of 137Cs contamination in both foodstuffs. The estimated effective doses received by adult members of the Croatian population due to the intake of radiocaesium by chicken meat and egg consumption for the overall observed period are very small, 2.0 and 0.6 µSv respectively. Therefore, chicken meat and chicken egg consumption was not a critical pathway for the transfer of radiocaesium to humans.

Assessment of multiple anthropogenic contaminants and their potential genotoxicity in the aquatic environment of Plitvice Lakes National Park, Croatia.

In this study, the influence of anthropogenic pollution on the aquatic environment of Plitvice Lakes National Park (PLNP) was investigated during 2011-2012 using a combination of chemical and cytogenetic analyses. Four groups of major contaminants [(volatile organic compounds: benzene, toluene, ethylbenzene, and xylenes (BTEX); persistent organochlorine pollutants: organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs); major and trace elements; anthropogenic radionuclides (90Sr, 134Cs, and 137Cs)] were determined in three aquatic compartments (water, sediment, fish). Mass fractions of inorganic constituents in different compartments reflected the geological background of the area, indicating their origin from predominantly natural sources. Levels of volatile and persistent organic compounds in water and fish, respectively, were very low, at levels typical for remote pristine areas. Analysis of anthropogenic radionuclides in water and sediment revealed elevated activity concentrations of 137Cs in water, and measurable 134Cs in the upper sediment layers from April 2011, possibly as a consequence of the Fukushima nuclear accident in March 2011. The potential genotoxicity of river and lake water and lake sediment was assessed under laboratory conditions using the alkaline comet assay on human peripheral blood lymphocytes, and measured levels of primary DNA damage were within acceptable boundaries. The results showed that despite the protected status of the park, anthropogenic impact exists in both its terrestrial and aquatic components. Although contaminant levels were low, further monitoring is recommended to make sure that they will not rise and cause potentially hazardous anthropogenic impacts.

The impact of multiple anthropogenic contaminants on the terrestrial environment of the Plitvice Lakes National Park, Croatia.

The anthropogenic impact on the terrestrial environment of the Plitvice Lakes National Park (PLNP) was investigated through the analysis of three groups of major contaminants (persistent organochlorine pollutants including 15 organochlorine pesticides (OCPs) and 17 polychlorinated biphenyls (PCBs), trace elements/heavy metals (6 major and 23 trace constituents), and anthropogenic radionuclides ((90)Sr, (134)Cs, and (137)Cs)) in three terrestrial compartments (soil, air, and bioindicators of air contamination) during 2011-2013. The correlation coefficients of element mass fractions with soil properties indicated that total Fe and Al minerals, soil organic matter (OM), and organic carbon (OC) content affected the mass fractions of most trace elements in the topsoils. The annual and spatial distributions of heavy metals in total deposited matter (TDM) indicated that the metals came from natural sources and long-range transfer of particulate matter. The PCB and OCP levels found in soil and conifer needles corresponded to global environmental pollution levels by persistent organic pollutants and represented the lower end of the mass fraction ranges reported in the relevant literature. Analyses of anthropogenic radionuclides in bioindicators (conifer needles, lichens, and mosses) showed low but measurable activity concentrations of (134)Cs (for the first time after the Chernobyl accident), which indicated origin from the March 2011 Fukushima Nuclear Power Plant accident. Our overall results indicated that human activity inside or near the PLNP had no significant impact either on contaminant spread by air or on their content in topsoils.

ESTIMATION OF AIRBORNE 106RU ACTIVITY CONCENTRATION FROM TOTAL BETA ACTIVITY OF PM10 PARTICLE FRACTIONS.

Airborne radioruthenium, as a result of an accidental release, presents a risk for occupational and public exposure. In fall 2017, a detection of 106Ru was reported by the European atmospheric radioactive contamination monitoring networks. We investigated the daily specific total beta activity of PM10 particle fractions samples. The presented method enables indirect determination of airborne 106Ru activity concentration from total beta activity, in case 106Ru was confirmed as single excess radiological pollutant. This allows for daily measurements and time-resolved 106Ru activity concentration data. We estimated the indicative committed effective dose due to 106Ru inhalation for the Croatian population during the exposure period. Although the estimated dose value of ~169.7 nSv, for ~6-d duration of ruthenium air pollution, was very low, it was ~40 times higher than the value for Hinh from inhalation of other radionuclides (90Sr + 137Cs + 40K + 7Be).

Baseline radioecological data for the soil and selected bioindicator organisms in the temperate forest of Plitvice Lakes National Park, Croatia.

The aim of this study was to provide baseline radioecological data for the temperate forest ecosystem in Plitvice Lakes National Park. Emphasis was placed on the determination of naturally occurring radionuclides since there is an acknowledged lack of data for these radionuclides in non-accident conditions in wildlife, even for bioindicator organisms. Activity concentrations of 238U, 226Ra, 210Pb, 232Th, 40K, 134Cs, and 137Cs were measured by gamma spectrometry in soil and bioindicators: earthworms, conifer needles, mosses, and lichens. From the measured activity concentrations, concentration ratios were calculated to quantify the transfer of these radionuclides from soil to bioindicators. Our results show that soil activity concentrations are biased toward results from other studies conducted within the Dinaric mountain region. However, in moss and lichen samples, we measured higher activity concentrations of 226Ra and lower activity concentrations of 40K and 137Cs in comparison to similar studies. Also, we estimated lower concentration ratios for all radionuclides from soil to these organisms, except for 210Pb, in comparison to generic values. The transfer of 238U was generally low for all of the bioindicator organisms. For conifer needles, a correlation was found between activity concentrations of 226Ra and 137Cs in soil and related concentration ratios. Correlation was also found between the activity concentration of 40K in soil and transfer of 40K and 137Cs to mosses and lichens. A comparison with literature data highlighted the lack of 226Ra related concentration ratios for conifer trees and especially for earthworms. Therefore, the results of this study could supplement the sparse data currently available on radionuclide background data in similar ecosystems and related soil-to-wildlife transfer of radionuclides. Dose rate assessments, performed by the ERICA Tool, estimated that 96% of the overall exposure of wildlife in the Park area is due to the background dose rates, while 0.06 µGy h-1 on average can be attributed as an incremental dose rate from 134Cs and 137Cs.

Radioactive contamination in Croatia by phosphate fertilizer production.

The contents of natural radionuclides (radium, uranium and potassium) were measured in the area of a phosphate fertilizer factory in central Croatia, as a part of extended and still ongoing monitoring program of radioactive contamination of human environment in Croatia that is performed by the Radiation Protection Unit of the Institute for Medical Research and Occupational Health in Zagreb. Activity concentrations in all analysed media (waste water, trickling water from piezometers, phosphogypsum deposit and final products) considerably fluctuated, especially in phosphogypsum and waste water. Mean (226)Ra activity concentration in waste phosphogypsum was measured to be 483+/-190 Bqkg(-1). Based on that value, it was estimated that 4 million m(3) of phosphogypsum that have been deposited up to now contain about 4.3 x 10(12) Bq, i.e. about 200 g of (226)Ra. However, effective dose for an adult that would be incurred by consumption of water from nearby wells was estimated to be 5.3+/-1.3 microSv. The results show that (226)Ra activities cause effective doses, which are below the recommended maximum as the estimated annual (226)Ra effective dose does not exceed 0.1 mSv as recommended by the World Health Organization.

Natural radioactivity of 226Ra and 228Ra in thermal and mineral waters in Croatia.

Thermal waters are known as valuable natural resources of a country. They contain certain degree of natural radioactivity attributable to the elements of the uranium and thorium natural decay series. Among these elements, the most radiotoxic and the most important is radium that exists in several isotopic forms (226Ra and 228Ra). The focus of attention was the content of radium in samples of thermal and mineral spring water from several spas in Croatia. These waters are mainly used for medical, bathing and recreational purposes, and some of them are used for drinking. Measured activity concentrations of 226Ra ranged from 87 to 6200 mBq l(-1) which, in some springs, exceed the maximal permissible level of 1 Bq l(-1) for drinking water. Measured activity concentrations of 228Ra ranged from 23 to 3480 mBq l(-1). The study showed that radium content for the investigated thermal and mineral waters is below the levels at which negative consequences would arise due to ingestion.

Long-term investigations of post-Chernobyl radiocaesium in fallout and air in North Croatia.

The long-term behaviour of (137)Cs activity concentrations in air and fallout has been studied in the city of Zagreb for the post-Chernobyl period (1986-2006) as a part of an extended monitoring program of radioactive contamination of human environment in Croatia. Annual mean (137)Cs activity concentrations in air and annual total deposition fluxes (wet plus dry) decreased from 2.8 x 10(-4) Bq m(-3) in September 1986 to 3.0 x 10(-6) Bq m(-3) in last quarter of 2006 and from 6,410 Bq m(-2) year(-1) in 1986 to 2 Bq m(-2) year(-1) in 2006 respectively. By fitting the measured (137)Cs activity concentrations to the theoretical curve the ecological half-lives of (137)Cs in air and fallout were estimated with respective values of 0.46 and 0.54 years for immediate post-Chernobyl period, increasing to 5.52 and 3.97 years afterwards. Using the data on (137)Cs activity concentrations in air and fallout total caesium deposition velocity of (3.34 +/- 3.13) x 10(-2) ms(-1) was estimated with median value being 2.13 x 10(-2) ms(-1). Such relatively high (137)Cs deposition velocities compared with pre-Chernobyl ones, are characteristic for the post-Chernobyl period and, according to Stokes' settling law, indicate that the diameters of aerosol particles associated with (137)Cs originated from the Chernobyl accident are pretty large, i.e. >1 microm. (134)Cs/(137)Cs activity ratio in fallout and in air has been found to be similar to the theoretically predicted values, initial value being about 0.5 and decreasing according to differential radioactive decay. The similar ratio has been observed in most of the other environmental samples.

Environmental radiological risk assessment of a coal ash and slag disposal site with the use of the ERICA Tool.

The aim of this study was to assess the environmental radiological risk of coal ash and slag to terrestrial wildlife. The research site used in this study was a disposal site of coal ash and slag with enhaced content of uranium decay chain radionuclides. With the use of the ERICA Tool, total dose rates to wildlife and risk of resultant radiobiological effects were estimated. As input data for the assessment, experimental activity concentrations of 238U, 226Ra and 210Pb in coal ash and slag and best estimates of activity concentrations for related daughter radionuclides and 235U decay chain were used. Where possible, the experimental data for activity concentrations of 238U, 226Ra and 210Pb in plants and related concentration ratios were used. Results were compared to background dose rates, also estimated by the Tool. The Tool's assessment data indicated internal exposure as the prevalent exposure pathway with 226Ra and 210Po as the main dose contributors. Also, the contribution of 235U decay chain to the total dose rate was not negligible since for some organisms it represented up to 11% of the total dose rate. The risk of an occurrence of radiobiological effects in plants on the coal ash and slag disposal site can be considered negligible since the estimated total dose rates were below the screening dose of 10 µGyh-1 and near the dose rates estimated for plants in the control area. However, the estimated dose rates for reference animals and Lichen & Bryophytes were above the screening dose rate for most organisms and on average 13 times higher than the estimated background dose rates. At the given dose rates, an occurrence of different radiobiological effects could not be excluded for animals in close contact with coal ash and slag such as earthworms and small burrowing mammals. A separate assessment performed on an example of reference plants showed that the use of activity concentrations in organisms as input data can result in an order of magnitude smaller estimates of dose rates in comparison to activity concentration in coal and ash as input data. Our study highlighted the need for experimental data in radiological risk assessments to mitigate the conservatism of the ERICA Tool and its tendency to overestimate dose rates.

Multi-element composition of soil, mosses and mushrooms and assessment of natural and artificial radioactivity of a pristine temperate rainforest system (Slavonia, Croatia).

This study investigates multi-element composition of soil, mosses and mushrooms from a pristine temperate rainforest (Prasnik, Croatia). Additionally, the activity levels of natural (238U, 235U and 232Th decay chains, 40K and 7Be) and anthropogenic (137Cs and 134Cs) radionuclides in the investigated soil samples, obtained by gamma spectrometry, provide baseline of environmental radioactivity levels in this area. The aim of investigation was to explore the uptake of metal(loid)s by bioindicator species (mosses, mushrooms) growing in a pristine environment characterized by naturally elevated concentration of metals. The calculated enrichment and bioaccumulation factors, correlations between different groups of elements and similar multi-element patterns in mosses, mushrooms and soil samples revealed the prevailing influence of the local substrate geochemistry on element concentrations in mosses and mushrooms. The results suggest atmospheric deposition of Bi, Cd and Pb, while radionuclide activities point to atmospheric fall-out (including global contamination by radiocaesium) and influence of the pedological substrate. The confined area of investigation, with limited variations in soil characteristics and geological composition, allowed clearer insight into the origin of metal(loid)s in mosses and mushrooms. On the other hand, using bioindicator species with different element uptake mechanisms enabled distinction between different sources of elements.

Radiocaesium contamination of beef in Croatia after the Chernobyl accident.

Long-term investigations of radiocaesium activity concentrations in beef in the Republic of Croatia are presented. The radiocaesium levels in beef decreased exponentially and the effective ecological half-life of 137Cs was estimated to be 0.57+/-0.06 years for 1986-1990 period and 5.21+/-0.27 years for the 1991-2005 period. For 1986-1990 period, the effective ecological half-life of 134Cs in was estimated to be about 0.69+/-0.05 while 134Cs activity concentrations after year 1990 were below the detection limit of the instruments. The 134Cs:137Cs activity ratio in beef has been found to be similar to the ratio that has been observed in other foodstuffs and environmental samples. Radioecological sensitivity for beef meat, i.e., the transfer coefficient from fallout to sample was estimated to be 1.15x 10(-2)Bqykg(-1)/(Bqm(-2)). For an adult member of Croatian population annual effective doses received by 134Cs and 137Cs intake due to consumption of beef are small, as per caput effective dose for the overall 1986-2005 period was estimated to be 24.6microSv. Consequently, after the Chernobyl accident beef consumption was not a critical pathway for the transfer of radiocaesium from fallout to humans in Croatia.

Mosses and some mushroom species as bioindicators of radiocaesium contamination and risk assessment.

Mosses, lichens, mushrooms are able to efficiently accumulate different radioactive elements from their environment to a much higher degree than other vegetation. They are sensitive bioindicators of radioactive contamination for various ecosystems, particularly in the event of a nuclear accident and uncontrolled emission oh fission products. Results of systematic, long-term measurements of 137Cs activities in mosses and in some edible mushroom species in North Croatia for the post-Chernobyl period (1986-2007) are summarized. The study was conducted in the Radiation Protection Unit of the Institute for Medical Research and Occupational Health in Zagreb, as a part of an extensive monitoring program of the Croatian environment. In the overall observed period the highest activity concentration of 137Cs deposited by fallout has been recorded in 1986, which is the year of Chernobyl accident, causing peak S7Cs activity concentration in moss of 8800 Bq/kg in May 1986. In the same period mean 137Cs activity concentration in grass was 390 Bq/kg. The highest value of 137Cs activity concentration in Cortinarius caperatus mushrooms of 1351 Bq/kg has been recorded in 1989. Fitting the measured 137Cs activity concentrations to the theoretical curve the ecological half-life of 137Cs in moss was found to be around 978 days, in grass around 126 days in the period 1986-1990, in Cortinarius caperatus mushroom around 5865 days (16.1 years). Regarding the risk assessment to Croatian population, due to consumption of mushrooms, the collective effective dose for Croatian population, estimated to be about 35 mSv per year, was found to be quite low. Therefore, it can be concluded that mushroom consumption was not a critical pathway for the transfer of radiocaesium from fallout to humans after the Chernobyl accident.

226Ra and 228Ra in Croatian rivers.

The presence of natural radionuclides in Croatian rivers emphasizes the need for its continuous monitoring. Therefore results of 226Ra and 228Ra determination in Croatian river waters are presented in this paper. 226Ra and 228Ra were chosen as a possible source of human exposure due to their high radio-toxicity. Fifty liters of river water samples were collected from the Danube, Drava, Sava, Krka and Neretva rivers twice a year from 2002 to 2006. It is showed that activity concentrations of 226Ra ranged from 6.54 mBq/L to 59.44 mBq/L and 228Ra activity concentrations ranged from 2.57 mBq/L to 20.76 mBq/L. The highest values of both 226Ra and 228Ra were measured in the river Drava, and the lowest values in the river Sava. Statistically significant differences were not observed between radium concentrations from two watersheds (the Black Sea and the Adriatic Sea watershed), nor between 226Ra/228Ra ratio in rivers individually. The number of collected samples is insufficient to make more statistically significant conclusions. However the data obtained in this study could be the baseline for evaluating possible future changes.

Long-term investigations of radiocaesium activity concentrations in carp in North Croatia after the Chernobyl accident.

Long-term investigations of radiocaesium activity concentrations in carp in the Republic of Croatia are presented. The radiocaesium levels in carp decreased exponentially and the effective ecological half-life of (137)Cs was estimated to be about 1 year during 1987-2002 and 5 years during 1993-2005. The observed (134)Cs:(137)Cs activity ratio in carp was found to be similar to the ratio observed in other environmental samples. The concentration factor for carp (wet weight) was estimated to be 128+/-74 Lkg(-1), which is in reasonable agreement with model prediction based on K(+) concentrations in water. Estimated annual effective dose received by adult members of the Croatian population due to consumption of carp contaminated with (134)Cs and (137)Cs are small: per capita dose from this source during 1987-2005 was estimated to be 0.5+/-0.2 microSv. Due to minor freshwater fish consumption in Croatia and low radiocaesium activity concentrations in carp, it can be concluded that carp consumption was not a critical pathway for the transfer of radiocaesium from fallout to humans after the Chernobyl accident.

Post-Chernobyl Investigations of Radiocesium Activity Concentrations in Cistern Waters along the Croatian Coast of the Adriatic Sea.

The results of long-term investigations into the post-Chernobyl period of radiocesium activity concentrations in cistern waters along the Croatian coast of the Adriatic Sea are presented. The Cs activity concentrations in cistern water samples were in excellent correlation with fallout activities. The observed mean residence time of Cs in cistern waters was estimated to be 6.9 ± 0.8 y. Cesium-137 radioecological sensitivity for the period 1988-1997 for cistern water was estimated to be 1.17 × 10 Bq y L/(Bq m). The annual total effective dose incurred by Cs and Cs that a hypothetical adult person drinking 1 L of cistern water per day would receive was estimated to be < 1 mSv in 1986, decreasing to 3.6 µSv in 2015.

Plant uptake of 238U, 235U, 232Th, 226Ra, 210Pb and 40K from a coal ash and slag disposal site and control soil under field conditions: A preliminary study.

The aim of this study was to investigate the uptake of 238U, 235U, 232Th, 226Ra, 210Pb and 40K by plants that grow on a coal ash and slag disposal site known for its higher content of naturally occurring radionuclides. Plant species that were sampled are common for the Mediterranean flora and can be divided as follows: grasses & herbs, shrubs and trees. To compare the activity concentrations and the resultant concentration ratios of the disposal site with those in natural conditions, we used control data specific for the research area, obtained for plants growing on untreated natural soil. Radionuclide activity concentrations were determined by high resolution gamma-ray spectrometry. Media parameters (pH, electrical conductivity and organic matter content) were also analysed. We confirmed significantly higher activity concentrations of 238U, 235U, 226Ra and 210Pb in ash and slag compared to control soil. However, a significant increase in the radionuclide activity concentration in the disposal site's vegetation was observed only for 226Ra. On the contrary, a significantly smaller activity concentration of 40K in ash and slag had no impact on its activity concentration in plant samples. The calculated plant uptake of 238U, 235U, 226Ra and 210Pb is significantly smaller in comparison with the uptake at the control site, while it is vice versa for 40K. No significant difference was observed between the disposal site and the control site's plant uptake of 232Th. These results can be the foundation for further radioecological assessment of this disposal site but also, globally, they can contribute to a better understanding of nature and long-term management of such disposal sites.

226Ra removal processes in Croatian water facilities.

Today, bottled and tap drinking water mainly originates from underground waters which might contain considerable amounts of naturally occurring radionuclides. One of the most toxic radionuclide in drinking water is 226Ra. Following the metabolism of calcium, it could be deposited into the bone where, in sufficient amount, it could cause bone sarcoma. Although current drinking water preparation techniques are not specifically designed for 226Ra removal they can reduce certain amounts of 226Ra. This paper presents the efficacy of standard water preparation processes (granular activated carbon, green sand and fixed-leaf filtrations) currently used by Zagreb water supply and two Croatian water bottlers in removing 226Ra. Compared with other studies, the results of our study show low to moderate efficacy in lowering the 226Ra concentration in drinking water. Even so, 226Ra concentrations still comply with the recommendation of the Word Health Organisation (WHO) and with Croatian legislation.

Public exposure to 226Ra in drinking water.

This paper presents a new method for calculating the effective dose of 226Ra regularly ingested with drinking water over a long period of time. The method is based on the assessment of cumulated 226Ra activity in the fraction retained in the whole body at time t (in days) after intake [so called m(t) value]. For modelling, simulation, and visualisation of the continuous intake of 226Ra by drinking water, we used the Simulink program package integrated with the Matlab. The dose assessment was performed for 226Ra activities of 5 mBq L(-1), 50 mBq L(-1), 1000 mBq L(-1) and 5000 mBq L(-1). The results suggest that 226Ra activities above 1000 mBq L(-1) produce effective doses which are below the recommended maximum. However, the potential effect of 226Ra activities of this extent is still unknown in children.

[Radioactive waste due to electric power and mineral fertiliser production]. / Otpad vezan uz proizvodnju elektricne energije i proizvodnju mineralnih gnojiva.

Radiation Protection Unit of the Institute for Medical Research and Occupational Health in Zagreb has been conducting systematic investigations of radioactive contamination of the Croatian environment by anthropogenic fission products as well as by naturally occurring radioactive material (NORM) since 1963. Several critical sites in Croatia were identified for NORM, that is, for slag and ash repositories from coal-fired power plants and phosphogypsum repository from a mineral fertilizer production plant. As the coals and phosphate ores contain naturally occurring radionuclides, especially the members of the uranium and thorium radioactive chains, utilising these materials in various industries only enhances their natural radioactivity in residual waste. Consequently, the resulting activity concentrations of natural radionuclides in waste material could be several times higher than in the adjacent soil. These deposited materials pose permanent risk of radiation exposure due to the long physical half-life of natural radionuclides (e.g., T 1/2 = 1600 years for 226Ra). Results of scientific investigations related to natural radioactivity are used in the recovery of slag and ash repositories and landfills, as well as in establishing regulatory criteria targeting import of coal and phosphate ores. In consequence, recently measured activity concentrations of natural radioactivity in imported materials used nowadays in coal-fired power plants are significantly lower than in previously used raw materials. Therefore, slag and ash can be used as additive materials in cement production.

Age-dependent dose assessment of 226Ra from bottled water intake.

Water may present a source of prolonged exposure to naturally occurring radionuclides. One of the most frequently occurring radionuclides in natural mineral and spring waters is 226Ra and its decay products. The contribution of drinking water to the total exposure is very small, at about 5% of the average effective dose attributable annually to natural background radiation, but that exposure contributes to the risk of adverse health consequences. In this study the mean values of 226Ra concentration determined in natural mineral and spring bottled waters range from 6 to 412 mBq L(-1), which is in accord with Croatian legislation. 226Ra effective doses per year from spring water consumption range up to 86 microSv, while 226Ra effective doses per year from mineral water consumption show much higher values. The highest 226Ra effective doses per year from mineral waters consumption, which are up to seven times higher than the dose recommended by WHO (100 microSv), were found in infants and teens. Based on this study, drinking of certain brands of bottled mineral water is not recommended for these age groups because assessed 226Ra effective doses per year exceed the recommended limits. From other research it is known that testosterone appears in elevated concentration during these life periods and affects bone calcification. Therefore, testosterone could affect the retention of 226Ra into the bone. To make more precise conclusions further research is necessary. Adults and especially elderly people are much less susceptible to the presence of 226Ra. According to the results obtained in this study, 226Ra effective doses per year assessed for these age groups were considerably lower (i.e., 10 microSv).