INTRODUCTION
Natural radioactivity originates both from members of the radioactive arrays of which 232Th, 238U and 235U are the originators, as well as 40K. In addition to the natural ones, under the influence of technology (or human action), some artificial radionuclides have been released into the environment. One of them is 137Cs (T1 / 2 = 30y), to which the occurrence in nature was largely caused by nuclear tests in the 60's and the Chernobyl accident in 1986 [1].
This forms the bond between the substrate and a given specimen. The transfer factor (TF) is used as a parameter for environmental transfer models that are useful in predicting the specific activity of radionuclides in agricultural crops [3]. The main factors that determine TF variability are the type of radionuclide, the type of plant, the type of soil (its characteristics) and the stable concentration of the element [4]. Factor transfer values depend on plant varieties and weather [5]. The results of research on transfer factors should show, provide a basis for theoretical explanations for the different adoption of elements that do not participate in physiological and biochemical processes in the plant [6]. Transport processes in the soil-plant system for the radionuclide group 226Ra, 40K, 232Th, 238U, 235U and 137 Cs are not well known in the Pcinja region. The aim of this paper was to show the first results of transfer factors in some woody perennial plants that are very important in the food chain [7].
METHODOLOGY
This paper presents the results of transfer of 226Ra, 40K and 232Th factors in perennial woody plants (beech, oak, mulberry, acacia, apricot, plum). The first tests in the Vranje region included sampling at three locations: Slivnica and Toplac during 2016. About 10 samples of arable forest land were sampled as well as 9 samples of woody perennial plants.
The preparation of soil samples involves the removal of mechanical impurities, stones and plant material, as well as drying at 105° for 24 h. The samples of the woody plant cultures were dried at room temperature and mineralized at 450°.
The radioactivity of the samples was determined by gamma spectrometry at the Institute for Nuclear Sciences Vinca in the Laboratory for Radiation and Environmental Protection.
The gamma spectrometry was performed on three high purity germanium (HPGe) detectors (CAN -BERRA) with relative efficiencies of 18 % (n-type), 20 % (p-type), and 50% (n-type). Resolution of all of the detectors was 1.8 keV at 1332 keV. Efficiency calibration for soil samples was performed using a reference radioactive material - a silicone resin matrix, Czech Metrological Institute, Praha, 9031-OL-420/12, total activity 41.48 kBq on 31. 08. 2012. (241Am, 109Cd, 139Ce, 57Co, 60Co, 203Hg, 88Y, 113Sn, 85Sr, 137Cs) [8].
The counting time was 60000 s. The results are presented with the expanded measurement uncertainty for the factor k = 2, with the level of confidence of 95% for normal distribution [8].
The TF was calculated according to eq. (1), defined as the ratio of specific activity of radionuclide in plant dry matter [Bq/kg] and specificactivity in soil [Bq/kg].
TF = Ab/As (1)
where Ab is the specific activity of the radionuclide in plant dry matter [Bq/kg] and Az – the specific activity of the radionuclide in soil [Bq/kg].
The absorbed dose rate of gamma radiation from the natural radionuclides in soil was calculated according studies [9]
D (nGyh-1) = 0.462*CRa +0.604*CTh + 0.0417*Ck (2)
where CRa is the specific activity of 226Ra in soil, CTh the specific activity of 232Th in soil, and CK the specific activity of 40K in soil. The annual effective dose was calculated according to [9]
DE (mSv)=0.7SvGy-1*0.2*365*24*D (3)
RESULTS AND DISCUSSION
Soil samples were taken from different depths, but the sampling depths were not the same at all locations. In some locations, soil samples were taken from a depth of 0-5 cm, 0-10 cm and 0-20 cm, Bujkovac; soil samples from the depth of 0-5 cm, 5-10 cm and 10-15 cm were taken at Slivnica site; while at the Toplac site, soil samples were taken from a depth of 0-20 cm and 0-40 cm (Table 2).
At the given locations, the values of the specific activity of the detected natural radionuclides do not differ in depth; the differences present are within the measurement uncertainty of the measurement results. Even the specific activity values of the 137Cs radionuclide produced do not differ in depth.
The specific activity values of the radionuclide 226Ra at all sites are in the range of 22 to 45 Bq/kg, while for 232Th they are in the range of 29 to 55 Bq/kg. In the case of 40K, specific activity values at all sites are in the range of 460 to 730 Bq/kg, while specific activity values are 238U in the range of 22 to 51 Bq / kg, and 235U in the range of 1.1 to 2.7 Bq/kg. The specific activity values of the 137Cs produced radionuclide are in the range of 7.2 to 17 Bq/kg. The cesium leaching and relocation processes can lead to a very uneven distribution of this radionuclide in one area. Regardless, the obtained specific activity values of 137Cs are low, so obviously no accumulation of this produced radionuclide in the soil occurred. The specific activity ratio of 235U/238U corresponds to natural uranium.
All the detected values of natural radionuclides by location do not differ significantly.
Minimum values of specific activity for 226Ra, 232Th, 238U and 235U were obtained at the Bujkovac location, and maximum values at the Toplac location. The obtained values of the specific activity of the detected radionuclides are characteristic of the soil and correspond to values from other areas of the former Yugoslavia [10]. The value of the specific 226Ra activity is lower at the Bujkovac location compared to other locations.
Table 3 shows the results of the specific activity of the detected radionuclides in samples of woody plants in [Bq / kg] of dry matter. Samples of woody plants, tree, (beech, oak, apricot, mulberry, cherry, plum conifer, acacia and hornbeam) were taken from three locations: Bujkovac, Slivnica and Toplac. The altitudes of these samples are different, with the Slivnica location having the highest altitudes, as shown in Table 1.
In samples of tested woody plants taken from locations (Bujkovac, Slivnica and Toplac) in the Pcinja region (Table 4), the specific activity values of the detected 226Ra radionuclides were in the range of 0.48 Bq/kg for mulberry tree up to 12 Bq/kg for beech wood; for 232Th they are in the range of 0.6 Bq/kg for oak wood in the Bujkovac and Slivnica locations, up to 3.4 Bq/kg for hornbeam in the Slivnica location. For all other samples of woody plants, the specific activity of 232Th is below the minimum detection limit.
In the case of radionuclides, the 40K values of specific activity in wood samples are in the range of 25 Bq/kg (hornbeam tree in Slivnica) to 120 Bq/kg for elm tree in Bujkovac. The specific activity values of radionuclides 238U, 235U for all wood samples at Toplac and Bujkovac locations are below the minimum detection limit. At the Slivnica site in acacia and beech wood samples, the values of these radionuclides are also below the minimum detection limit.
Only at the Slivnica site, specific activity values of radionuclides 238U and 235U were detected in oak and hornbeam samples above the detection limit. The specific activity ratio of 235U/238U corresponds to natural uranium. In the case of the 137Cs radionuclide produced, the value of the specific activity is below the minimum detection limit in the apricot tree sample at the Toplac site, as well as in the acacia, cherry and elm tree samples at the Bujkovac site. The specific activity of the detected 137Cs radionuclide for the apricot tree per is 47 Bq/kg which is much higher than in the apricot tree sample examined.
Unlike other wood samples, cera wood has the least activity-specific values for 232Th, 40K, 238U, 235U and 137Cs. The maximum value of specific activity of 226Ra of 12 Bq/kg was detected in the beech sample at the site Slivnica, while the minimum value of specific activity of this radionuclide was 0.48 Bq/kg was detected in the mulberry sample at the Bujkovac location. For 232Th radionuclides, the maximum value of specific activity of 3.4 Bq/kg was detected in the gabbro sample at Slivnica site, and the minimum value of 1 Bq/kg was detected in oak at the same location.
The minimum value of specific activity of 40K radionuclide of 25 Bq/kg was detected in the hornbeam sample at Slivnica site, and the maximum value of 120 Bq/kg was detected in the elm sample at Bujkovac site. A maximum activity value of 235U of 0.2 Bq/kg at the Slivnica site was detected in the hornbeam sample. At the same location in the
oak sample, the specific activity of this radionuclide has a minimum value of 0.16 Bq/kg.
The maximum value of 137Cs specific activity was detected in the beech sample of 0.9 Bq / kg at the Slivnica site, while the minimum values of 0.09 Bq/kg were detected in the plum bean sample at the Bujkovac site.
The obtained values of transfer factor for woody plant samples are given (Table 5).
In most samples of woody cultures, natural radionuclides 238U and 235U were not detected, that is, their specific activities are below the minimum detection limit. The transfer factor is only determined for: 40K, 226Ra, 232Th. Higher transfer factor values were obtained by 40K for samples of oak, plum, hay, elm, cherry and acacia compared to other radionuclides and ranged from 0.09 to 0.24 [11]. Higher values of transfer factors were obtained for 226Ra in the beech sample, Bujkovac site, 0.46 compared to other woody plants.
CONCLUSION
Specific soil radionuclide activities at all sites ranged from 22 to 45 Bk/kg for 226Ra, 29 to 55 Bk / kg for 232Th, 460 to 730 Bk/kg for 40K, 22 to 51 Bk/kg for 238U, from 1.1 to 2.7 Bk/kg for 235U, and 7.2 to 17 Bk / kg for 137Cs. The differences between the specific activities of radionuclides in soil samples from different depths are within different ratios, and the specific activity values of radionuclides 235U/ 238U are of uranium origin.
The activities of the radionuclides tested do not differ in general from the values given by other authors in their tests [12].
The distribution of radionuclides from soil to soil and in the plant depends on the bioavailability of at least other quantities in the soil, root structure, habitat only, as well as the processes that take place in the plant. Which were the only ones that gave some significant results in the measurement. Examination of soil samples and woody perennials yielded results showing that the transfer factor behaves according to a certain probability distribution. It can be concluded that the transfer factor obtained for 40K compared to other radionuclides has higher values. This means that the largest number of plants (tree trunks) absorb between 0.02-0.46%226Ra and about 0.6-0.24%40K [13].
These are the first studies of transfer factors for some cereals grown in the Pcinja district. Since the results of the transfer factors are determined only for some types of cereals taken from the soil of the type of manure, I suggest further research, but for some other type of land, to make sure that the Pcinja district is a region that can produce healthy food.
1. Bikit I (2012) Monitoring of radioactivity of land in the City of Novi sad during 2012 (in Ser bian). Faculty of Science, University of Novi Sad, Serbia.
2. Mitrovic B, Andrić V, Ajtić J, Lazić M, Krstić N (2016) Natural and anthropogenic radioactivity in the environment of kopaonik moun tain. Serbia Environ Pollut 215: 273-279.
3. Pulhani VA (2005) Uptake and distribution of natural radioactivity in wheat plants from soil. J Environ Radioact 79: 331-346.
4. Schimmack W, Kracke W, Sommer M (2003) Spatial variabil ity of fall out 90sr in soil and vegetation of an alpine pasture. J Environ Radioact 65: 281-296.
5. Djelic G, Krstic D, Stajic J, Milenkovic B, Topuzovic M, et al. (2016) Transfer factors of natural radionuclides and 137cs from soil to plants used in traditional medicine in central Serbia. J Environ Radioact 158: 81-88.
6. Popovic D, Bozic T, Stevanovic J, Frontasyeva M, Todorovic D, et al. (2010) Concentration of trace elements IN blood and feed of home bred animals in Southern Serbia. Environ Sci Pollut Res Int 17: 1119-1128.
7. Popovic D, Todorovic D, Frontasyeva M, Ajtic J, Tasic M, et al. (2008) Radionuclides and heavy metals in borovac, Southern Serbia. Environ Sci Pollut Res 15: 509-520.
8. Nikolic JD, Jokovic D, Todorovic D, Rajacic M (2014) Application of GEANT4 simulation on calibration of HPGe De tectors for cylindrical environmental samples. J Radiol Prot 34: N47-N55.
9. Jia G, Belli M, Sansone U, Rosamilia S, Gaudino S (2006) Concentration and character is tics of depleted uranium in biological and water samples collected in bosnia and Herzegovina. J Environ Radioact 89: 172-187.
10. Mitchell N, Sanchez DP, Thorne MC (2013) A review of the behaviour of 238U series radionuclides in soils and plants. J Radiol Prot 33: R17-R48.
11. Alsaffar MS, Jaafar MS, Norlaili AK, Ahmad N (2015) Distribution of 226Ra, 232Th, and 40K in rice plant components and physico-chemical effects of soil on their transportation to grains. J Radiat Res Appl Sc 3: 300-310.
12. Markovic J, Stevovic S, Rajacic M, Todorovic D (2016) Transfer factors for the “soils-cereals” system in the region pcinja serbia. Nucl Techno Radiat 31: 376-381.
13. Vera TF, Rodríguez MPB, Lozano JC (2003) Soil-to-plant transfer factors for natural radionuclides and stable elements in a mediterranean area. J Environ Radioactiv 65: 161-175.