Accumulation of 137Cs and 90Sr radionuclides by dominants and co-dominants of birch-pine forest communities in Northern Ukraine
iForest - Biogeosciences and Forestry, Volume 17, Issue 6, Pages 386-393 (2024)
doi: https://doi.org/10.3832/ifor4577-017
Published: Dec 20, 2024 - Copyright © 2024 SISEF
Research Articles
Abstract
Investigation of the post-Chernobyl accumulation of radionuclides in forest communities not only sheds light on the specific ecological aftermath of the disaster but also holds broader significance for enhancing our knowledge of radioactive contamination in natural environments and informing strategies for mitigating its impacts. The study was carried out in an area with soil contamination exceeding the pre-accident level for the isotopes cesium (137Cs, 5.0-15.0 Ci km-2) and strontium (90Sr, 0.15-3.0 Ci km-2) in the Semenivka State Forestry (Chernihiv Region, Northern Ukraine). Four experimental plots with an area of 400 m2 each were established in a birch-Scots pine forest, where dominant trees, herb and shrub layers, and mosses were analyzed for radionuclide bioaccumulation. Our results indicate a larger accumulation of 137Cs compared to 90Sr in the forest ecosystem. The highest 137Cs and 90Sr accumulation was detected in the fern Pteridium aquilinum, and the lowest in Pinus sylvestris. Based on our results, we hypothesized that the processes of accumulation and dispersion of 137Cs among the different vegetation layers are more complex compared to 90Sr. MANOVA regression analysis revealed significant differences in the accumulation of radionuclides between different layer levels, plant species and plant parts in the studied forest areas. According β coefficient analysis, both 137Cs and 90Sr are influenced by the site (area type) but in different ways. For 90Sr, the negative β coefficient implies that certain area types are associated with lower Sr accumulation, while for 137Cs the effect of area type may be more complex or context-dependent. These contrasting results suggest that Cs accumulation is more sensitive to changes in layer level compared to Sr. This could be due to differences in the environmental behaviour of these radionuclides, their chemical properties or differences in soil-plant transfer mechanisms. The significant effect of plant species on 137Cs/90Sr accumulation highlights that species-specific characteristics may play a role in radionuclide uptake. Moreover, we found significant differences in 137Cs/90Sr accumulation between different plant parts. Further research on the mechanisms of accumulation and distribution of these radionuclides are essential for better understanding their impact on human health and the environment.
Keywords
Forest Vegetation, Peucedano-Pinetum, Polesie, Radioactive Contamination, Radiocesium (137Cs), Radiostrontium (90Sr)
Introduction
Research on the accumulation of radiocesium (137Cs) and radiostrontium (90Sr) in forest communities has particular significance in the context of the Chernobyl disaster in Ukraine. The Chernobyl nuclear power plant disaster in 1986 resulted in the release of large quantities of radioactive materials into the environment, including 137Cs and 90Sr, which persisted in the ecosystems for decades. Nowadays, the ecological situation in the Ukrainian Polesie forests is complicated by the contamination of a vast area with radionuclides resulting from a mixture of products of nuclear decay and neutron activation ([5]).
Forests captured more than 80 percent of the Chernobyl-derived radionuclides, the most long-lived being 137Cs, 239Pu, 240Pu, 241Pu, and 90Sr. Forest ecosystems incorporate the radioactive material into their biological processes, moving within woody plants/forest litter and soil/woody plant systems in stable annual cycles ([10]). Most of the radiocesium was initially trapped in the leaves and branches and then transferred to the forest floor through litterfall and rain in the first few years. A small percentage of the total amount of radiocesium in the forest is absorbed from soil by trees and eventually returns to the ground surface as litterfall; in other words, it is cycling in the forest. At present, most of the radiocesium has been transferred to mineral soil, and its circulation in the forest is slow ([6]).
The bioaccumulation of radionuclides by plants may occur by two modes: foliar absorption by plant leaves and shoots, or root uptake from the soil. 90Sr and 137Cs are readily absorbed by leaves, but 137Cs is translocated more into fruits and seeds than 90Sr, as the latter tends to remain in the plant part where it was initially absorbed ([11]). Studies have been conducted on the accumulation and distribution of radionuclides in Pinus sylvestris ([16], [7], [8], [9], [20]). The main distribution patterns of radionuclides in the trunk do not significantly change with time ([8]). The distribution of 137Cs in Betula pendula wood shows a stronger dependence on site characteristics and the longevity of trees compared to Pinus sylvestris ([20]).
In the Chernihiv region, land contamination is mainly due to the long-lasting radionuclides 137Cs and 90Sr resulting from the Chernobyl disaster. The total area contaminated by 137Cs (above 1 Ci km-2) is 174.72 thousand ha, including forests (102.70 thousand ha) and agricultural land (72.02 thousand ha), while 97% of the area is contaminated by 90Sr above the threshold of 0.02 Ci km-2. More than 19% of state forests are radioactively contaminated, and 11 state forestry farms are contaminated with 137Cs above 1 Ci km-2. All forestry farms are contaminated with 90Sr above 1 Ci km-2 ([5]).
Studying the accumulation of these radionuclides in the forest communities surrounding the Chernobyl Exclusion Zone provides valuable insights into the long-term ecological consequences of nuclear accidents. Forest ecosystems play a crucial role in the retention and redistribution of radionuclides, affecting their transfer to soil, vegetation, wildlife, and ultimately humans through food chains. Therefore, understanding the dynamics of post-Chernobyl radionuclide accumulation in forest ecosystems is essential for assessing the ongoing environmental risks and developing effective management strategies.
This investigation aims to provide knowledge and tools to guide decisions on monitoring and remediation of contaminated areas, as well as to inform land use policies to reduce human radiation exposure. Moreover, studying the accumulation of 137Cs and 90Sr in forest communities provides a better understanding of the mechanisms driving the persistence and mobility of radioactive contaminants in terrestrial environments. This knowledge is crucial for predicting the long-term behavior of radionuclides in similar forest ecosystems affected by nuclear accidents worldwide, contributing to global efforts in nuclear safety and environmental protection.
The mobility and bioavailability of radionuclides of accidental origin in the terrestrial and aquatic environment are affected by both their chemical forms in the fallout and site-specific environmental characteristics, which determine the rate of leaching, fixation-remobilization, and absorption-desorption of the mobile fraction ([1]).
Pine and birch-pine forests of the Peucedano-Pinetum W. Mat. (1962) 1973 association are the most widespread in the Ukrainian Polesie, primarily established on sandy deposits ([13]). In Scots pine (Pinus sylvestris L.) forests, large fractions of total radionuclide depositions can be found in the aboveground biomass and litter ([8]). The possibility of economic utilization of forest products in radioactively contaminated areas depends on the compliance of radionuclide activity concentrations in plant tissues with the norms or national standards established by governments or regulators ([8]). This highlight the need of considering the different forest stand components (stems, leaves, shoots, roots, fruits, etc.) as repositories of biologically mobile radionuclides such as 90Sr and 137Cs.
The role of plants in monitoring radionuclides serves two purposes: to indicate recent atmospheric releases of radionuclides and to reflect the long-term behavior of aged radionuclide deposits in the soil. ([11]). Data on the accumulation of radionuclides in plants of different ecological and taxonomic groups are crucial for understanding the long-term dynamics of radionuclides in the entire forest ecosystem. Special attention should be paid to the radionuclide content in plants with the largest biomass (dominant and co-dominant species).
This study aimed at the analysis of radiocesium and radiostrontium accumulation in forest ecosystems by investigating the differences in the accumulation of radionuclides among different layer levels, plant species, and plant parts within specific forest areas and also evaluate the main effects of the area type, layer level, plant species (dominants and co-dominants of birch-pine forest communities), and plant part on radionuclide accumulation using a modeling approach.
Material and methods
Field research
A preliminary study was carried out in 2015 in areas of soil contamination exceeding the pre-accident level of two radioisotopes: cesium (137Cs, from 5.0 to 15.0 Ci km-2), and strontium (90Sr, from 0.15 to 3.0 Ci km-2 - [23]). The study area is located in the Bleshnya and Orlykivka forestry of the Semenivka State Forestry (Chernihiv Region, Northern Ukraine), which is known to be the most contaminated region in northern Ukraine following the Chernobyl accident.
Four experimental plots (~400 m2) were selected and georeferenced using a Garmin eTrex™ 10 GPS receiver (Garmin Ltd., Olathe, KS, USA). Soil samples were collected according with the sampling methods for radiation control ([15]). Soil samples (each about 1 kg) were taken from 10 randomly chosen points in each plot (n=10), combined to obtain one cumulative sample per plot, and then measured for contamination.
All plots were established in birch-pine forests belonging to the Peucedano-Pinetum W. Matuszkiewicz (1962) 1973 association of the Dicrano-Pinion sylvestris (Libbert 1933) W. Matuszkiewicz 1962 alliance of the Pinetalia sylvestris Oberd. 1957 order of the Vaccinio-Piceetea Br.-Bl. in Br.-Bl. et al. 1939 class. In all areas, the birch-pine forests were formed on sandy soils. The four experimental plots were homogeneous in terms of age (50-70 years), floristic composition, and structure of phytocoenoses but differed in the levels of soil radiation contamination.
Plot 1 (Baranivka) is located 1.4 km north of Baranivka village on the right-bank pine terrace of the Revna River (52.0689° N, 32.2931° E, 136 m a.s.l. - Fig. 1). Based on the measurements of the radionuclide activity in the collected soil samples, the soil depositions were estimated at 328 ± 21.56 Bq kg-1 of 37Cs and 2011 ± 241.47 Bq kg-1 of 90Sr.
Plot 2 (Bleshnya) is located 1.0 km north of Bleshnya village on the left-bank pine terrace of the Snov River (52.1361° N, 32.3403° E, 130 m a.s.l. - Fig. 1). The radionuclide activity of the soil samples was 354 ± 26.33 Bq kg-1 of 37Cs and 2326 ± 284.28 Bq kg-1 of 90Sr.
Plot 3 (Orlykivka) is located 1.2 km north of Orlykivka village on the right-bank pine terrace of the Revna River (52.0776° N, 32.4167° E, 145 m a.s.l. - Fig. 1). The radioactive contamination of the soil samples from this experimental plot is 387 ± 27.82 Bq kg-1 of 37Cs and 927 ± 178.23 Bq kg-1 of 90Sr.
Plot 4 (Mohy) is located 2.8 km east of Mohy village on the right-bank pine terrace of the Revna River (52.0776° N, 32.4167° E, 145 m a.s.l. - Fig. 1). The contamination in the soil was 380 ± 25.12 Bq kg-1 of 37Cs. The 90Sr activity in the soil was 1003 ± 221.16 Bq kg-1 of 90Sr.
Vegetation sampling
The vegetation relevés were taken during the optimum vegetation period (Jun-Aug 2015). The forest layers and the projective coverage of trees and understory species in each plant community was determined according to Yakubenko et al. ([26]). Syntaxa were identified according to Matuszkiewicz ([14]).
Plant material for radiological analysis was collected from each plot. The tree layer was primarily dominated by Betula pendula Roth and Pinus sylvestris L., covering 40%-60% of the area. In the shrub layer, Frangula alnus Mill. was the dominant species, making up 30%-40% of the coverage, while Pteridium aquilinum (L.) Kuhn was a co-dominant species, accounting for 15%-20% of the cover in the herb layer. In the dwarf shrub layer, Vaccinium myrtillus L. was dominant (covering 40-60%) and Calluna vulgaris (L.) Hill co-dominant (15-20%). The plant community was also characterized by a moss layer with a projective cover of 50-75%. In this layer, Pleurozium schreberi (Willd. ex Brid.) Mitt. was the dominant species covering 40-65%, while Ptilium crista-castrensis (Hedw.) De Not. was co-dominant, accounting for 10-15%. All dominant and co-dominant species were selected for further analyses (Fig. 2).
Fig. 2 - Plant species included in the study and their allocation by layers. Plant species: 1 - Pinus sylvestris, 2 - Betula pendula, 3 - Frangula alnus, 4 - Pteridium aquilinum, 5 - Vaccinium myrtillus, 6 - Calluna vulgaris, 7 - Pleurozium schreberi, 8 -Ptilium crista-castrensis. Phytocenosis layers: I - tree layer , II - shrub layer , III - herb layer, IV - dwarf shrub layer, V - mosses layer. The circles show parts of plants that were selected for radiological analysis.
In each experimental plot, samples of vegetative plant organs were collected in 10 replicates for each component within a species. Ten samples were taken from each compartment, and one sample was obtained from each individual plant ([25]). The 137Cs content determination in the plant samples and soil was performed using a Gamma plus U spectrometer (Expert Center, Russia), whereas the 90Sr content determination was carried out with a radiometric ending at α-β detector CANBERRA-2400® (Mirion Technologies Inc., Atlanta, GA, USA).
Statistical analysis
The Statistica v. 13.3 package (TIBCO Software, Palo Alto, CA, USA) was used for statistical analysis and the results were expressed as means ± standard deviation. Significant differences between the means were determined using a multiple-range test, with p-values < 0.05 considered significant. The data were tested for homogeneity of variance using Levene’s test, and normality was checked with the Kolmogorov-Smirnov test.
Differences in the accumulation of radionuclides (in terms of 137Cs/133Cs ratios) among different layer levels, plant species (including Betula pendula Roth, Pinus sylvestris, Frangula alnus, Pteridium aquilinum, Vaccinium myrtillus. Calluna vulgaris, Pleurozium schreberi, and Ptilium crista-castrensis), and plant parts in the four plots were analyzed using four-way ANOVA and Tukey’s post-hoc test. The application of multivariate significance tests for the main effects (plot type, layer level, plant species, and plant part) on radionuclide accumulation enabled to estimate the mean value of the dependent variable, the main effect, and the experimental random error using the F-test. We have also used the concept of the maximum permissible specific activity (MPSA, 100%) as a point of reference for our comparisons. The multiple correlation coefficient (R), the coefficient of determination (R2), and its corrected form reduced by random errors (R2 adjusted) were obtained from MANOVA analysis. For each predictor variable (area, layer level, plant species, and plant part), the beta coefficient (β) of a regression model was used to indicate the magnitude and direction of its effect on the dependent variables (accumulation of 137Cs and 90Sr radionuclides).
Results
The 137Cs and 90Sr specific activity in the plant samples and its dependence on the layer level, plant species (Betula pendula, Pinus sylvestris, Frangula alnus, Pteridium aquilinum, Vaccinium myrtillus, Calluna vulgaris, Pleurozium schreberi, n=10), and plant part in the experimental plots Baranivka (1), Bleshnya (2), Orlykivka (3), and Mohy (4) are presented in Tab. 1, Tab. 2, Tab. 3and Tab. 4, respectively.
Tab. 1 - The accumulation of 137Cs and 90Sr radionuclides (in Bq kg-1) in plot 1 according to layer, species and plant part in Bleshnya and Orlykivka forests of the Semenivka State Forestry (Chernihiv Region, Northern Ukraine). The mean ± standard error (SE) are presented (n = 10). Significant differences (p<0.05) of each mean with other plant species groups after post-hoc Tuckey test are indicated by numbers in superscript. Plant species groups: 1 Betula pendula and Pinus sylvestris; 2 B. pendula and Frangula alnus; 3 B. pendula and Pteridium aquilinum; 4 B. pendula and Vaccinium myrtillus; 5 B. pendula and Calluna vulgaris; 6 B. pendula and Pleurozium schreberi; 7 B. pendula and Ptilium crista-castrensis; 8 Pinus sylvestris and F. alnus; 9 P. sylvestris and P. aquilinum; 10 P. sylvestris and V. myrtillus; 11 P. sylvestris and C. vulgaris; 12 P. sylvestris and P. schreberi; 13 P. sylvestris and P. crista-castrensis; 14 F. alnus and P. aquilinum; 15 F. alnus and V. myrtillus;16 F. alnus and C. vulgaris; 17 F. alnus and P. schreberi; 18 F. alnus and P. crista-castrensis;19 P. aquilinum and V. myrtillus; 20 P. aquilinum and C. vulgaris; 21 P. aquilinum and P. schreberi; 22 P. aquilinum and P. crista-castrensis; 23 V. myrtillus and C. vulgaris;24 V. myrtillus and P. schreberi; 25 V. myrtillus and P. crista-castrensis;26 C. vulgaris and P. schreberi; 27 C. vulgaris and P. crista-castrensis;28 P. schreberi and P. crista-castrensis.
Radio nucl. |
Layer | Plant species | Plant part | Mean ± SE | Min | Max | Variance | Skewness |
---|---|---|---|---|---|---|---|---|
137Cs | Tree | - | branches with leaves | 135.00 ± 13.47 | 112 | 154 | 181.56 | -0.32 |
Tree | Pinus sylvestris | branches with needles | 95.00 ± 12.99 1 | 81 | 123 | 168.67 | 1.30 | |
Shrub | Frangula alnus | branches with leaves | 296.00 ± 27.05 2.8 | 251 | 329 | 731.78 | -0.54 | |
Herb | Pteridium aquilinum | leaves | 215.00 ± 22.52 3.9.14 | 184 | 252 | 507.11 | 0.23 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 210.00 ± 23.66 4.10.15 | 180 | 252 | 559.78 | 0.50 | |
Dwarf shrub | Calluna vulgaris | shoots | 223.00 ± 25.95 5.11.16 | 186 | 264 | 673.56 | 0.32 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 223.00 ± 30.70 6.12.17 | 187 | 277 | 942.22 | 0.68 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 132.00 ± 15.48 13.28 | 113 | 158 | 239.56 | 0.47 | |
90Sr | Tree | Betula pendula | branches with leaves | 1050.00 ± 94.72 | 920 | 1220 | 8972.22 | 0.64 |
Tree | Pinus sylvestris | branches with needles | 450.00 ± 51.69 1 | 365 | 535 | 2672.22 | 0.27 | |
Shrub | Frangula alnus | branches with leaves | 670.00 ± 84.75 2.8 | 545 | 805 | 7183.33 | -0.01 | |
Herb | Pteridium aquilinum | leaves | 2364.00 ± 341.20 3.9.14 | 1864 | 2765 | 116417.67 | -0.39 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 1210.00 ± 213.25 4.10.15.19 | 896 | 1470 | 45477.11 | -0.53 | |
Dwarf shrub | Calluna vulgaris | shoots | 1520.00 ± 217.96 5.11.16.20.23 | 1194 | 1875 | 47505.56 | 0.24 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 2005.00 ± 256.20 6.12.17.24.26 | 1647 | 2520 | 65639.78 | 0.81 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 1884.00 ± 230.25 7.13.18.25.27 | 1574 | 2225 | 53016.89 | 0.19 |
Tab. 2 - The accumulation of 137Cs and 90Sr radionuclides (in Bq kg-1) in plot 2 according to layer, species, and plant part in Bleshnya and Orlykivka forests of the Semenivka State Forestry (Chernihiv Region, Northern Ukraine). The mean ± standard error (SE) are presented (n = 10). Significant differences (p<0.05) of each mean with other plant species groups after post-hoc Tuckey test are indicated by numbers in superscript. For plant species groups, see Tab. 1.
Radionucl. | Layer | Plant species | Plant part | Mean ± SE | Min | Max | Variance | Skewness |
---|---|---|---|---|---|---|---|---|
137Cs | Tree | Betula pendula | branches with leaves | 160.00 ± 15.55 | 127 | 180 | 241.88 | -1.15 |
Tree | Pinus sylvestris | branches with needles | 125.00 ± 11.151 | 108 | 143 | 124.22 | 0.24 | |
Shrub | Frangula alnus | branches with leaves | 320.00 ± 28.212.8 | 289 | 374 | 795.78 | 0.70 | |
Herb | Pteridium aquilinum | leaves | 236.00 ± 30.323.9.14 | 194 | 284 | 919.56 | 0.23 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 179.00 ± 16.484.10.15.19 | 147 | 201 | 271.56 | -0.62 | |
Dwarf shrub | Calluna vulgaris | shoots | 165.00 ± 14.79 5.11.16.20.23 | 132 | 182 | 218.89 | -1.22 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 142.00 ± 24.70 6.17.21.26 | 115 | 178 | 610.22 | 0.44 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 144.00 ± 16.70 7.13.18.22.28 | 114 | 172 | 278.89 | -0.33 | |
90Sr | Tree | Betula pendula | branches with leaves | 1200.00 ± 296.64 | 830 | 1600 | 87993.56 | -0.19 |
Tree | Pinus sylvestris | branches with needles | 510.00 ± 76.16 1, | 385 | 738 | 4307.45 | 0.36 | |
Shrub | Frangula alnus | branches with leaves | 684.00 ± 80.04 2.8 | 564 | 819 | 6406.44 | 0.52 | |
Herb | Pteridium aquilinum | leaves | 2860.00 ± 378.49 3.9.14 | 2380 | 3393 | 143256.00 | 0.37 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 1367.00 ± 222.37 4.10.15.19 | 1006 | 1715 | 49448.89 | 0.16 | |
Dwarf shrub | Calluna vulgaris | shoots | 1734.00 ± 223.66 5.11.16.20.23 | 1394 | 2074 | 50026.00 | 0.15 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 2141.00 ± 317.84 6.12.17.21.24.26 | 1702 | 2563 | 101022.90 | -0.18 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 1985.00 ± 370.23 7.13.18.22.25.27.28 | 1390 | 2610 | 137068.90 | 0.05 |
Tab. 3 - The accumulation of 137Cs and 90Sr radionuclides (in Bq kg-1) in plot 3 according to layer, species, and plant part in Bleshnya and Orlykivka forests of the Semenivka State Forestry (Chernihiv Region, Northern Ukraine). The mean ± standard error (SE) are presented (n = 10). Significant differences (p<0.05) of each mean with other plant species groups after post-hoc Tuckey test are indicated by numbers in superscript. For plant species groups, see Tab. 1.
Radionucl. | Layer | Plant species | Plant part | Mean ± SE | Min | Max | Variance | Skewness |
---|---|---|---|---|---|---|---|---|
137Cs | Tree | Betula pendula | branches with leaves | 204.00 ± 22.66 | 169 | 244 | 513.56 | 0.13 |
Tree | Pinus sylvestris | branches with needles | 73.00 ± 8.25 1 | 610 | 860 | 68.00 | 0.16 | |
Shrub | Frangula alnus | branches with leaves | 352.00 ± 40.07 2.8 | 286 | 412 | 1605.78 | -0.35 | |
Herb | Pteridium aquilinum | leaves | 243.00 ± 28.42 3.9.14 | 205 | 297 | 807.78 | 0.29 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 198.00 ± 21.65 10.15 | 156 | 232 | 468.89 | -0.36 | |
Dwarf shrub | Calluna vulgaris | shoots | 154.00 ± 21.21 5.11.16.20.23 | 118 | 179 | 450.00 | -0.61 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 135.00 ± 19.69 6.12.17.21.24 | 109 | 171 | 387.78 | 0.50 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 138.00 ± 19.68 7.13.18.22.25.28 | 113 | 169 | 387.11 | 0.28 | |
90Sr | Tree | Betula pendula | branches with leaves | 402.00 ± 51.94 | 315 | 482 | 2697.78 | -0.28 |
Tree | Pinus sylvestris | branches with needles | 461.00 ± 58.20 1 | 345 | 532 | 3387.56 | -0.64 | |
Shrub | Frangula alnus | branches with leaves | 212.00 ± 26.15 2.8 | 180 | 255 | 683.78 | 0.43 | |
Herb | Pteridium aquilinum | leaves | 728.00 ± 105.22 3.9, 4 | 562 | 865 | 11071.11 | -0.61 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 415.00 ± 60.50 4.10.15.19 | 325 | 510 | 3660.44 | -0.01 | |
Dwarf shrub | Calluna vulgaris | shoots | 578.00 ± 77.85 5.11.16.23 | 452 | 701 | 6060.89 | -0.13 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 790.00 ± 82.50 6.12.17.21.24.26, | 650 | 945 | 6805.56 | 0.21 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 780.00 ± 67.33 7.13.18.22.25.27.28 | 632 | 848 | 4534.00 | -0.59 |
Tab. 4 - The accumulation of 137Cs and 90Sr radionuclides (in Bq kg-1) in plot 4 according to layer, species, and plant part in Bleshnya and Orlykivka forests of the Semenivka State Forestry (Chernihiv Region, Northern Ukraine). The mean ± standard error (SE) are presented (n = 10). Significant differences (p<0.05) of each mean with other plant species groups after post-hoc Tuckey test are indicated by numbers in superscript. For plant species groups, see Tab. 1.
Radionucl. | Layer | Plant species | Plant part | Mean ± SE | Min | Max | Variance | Skewness |
---|---|---|---|---|---|---|---|---|
137Cs | Tree | Betula pendula | branches with leaves | 212.00 ± 23.99 | 187 | 268 | 575.33 | 1.48 |
Tree | Pinus sylvestris | branches with needles | 146.00 ± 15.25 1 | 123 | 165 | 232.44 | -0.19 | |
Shrub | Frangula alnus | branches with leaves | 348.00 ± 34.18 2, 8 | 286 | 409 | 1168.44 | -0.13 | |
Herb | Pteridium aquilinum | leaves | 228.00 ± 31.04 3, 9, 14 | 186 | 274 | 963.56 | 0.27 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 206.00 ± 27.38 4, 10, 15, 19 | 168 | 243 | 749.56 | -0.07 | |
Dwarf shrub | Calluna vulgaris | shoots | 177.00 ± 23.36 11, 16, 20 | 138 | 213 | 545.78 | -0.11 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 133.00 ± 13.16 6, 17, 21, 24, 26 | 114 | 151 | 173.11 | 0.10 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 141.00 ± 18.32 7, 13, 18, 22, 25, 28 | 112 | 173 | 335.56 | 0.06 | |
90Sr | Tree | Betula pendula | branches with leaves | 456.00 ± 54.11 | 380 | 528 | 2927.78 | -0.60 |
Tree | Pinus sylvestris | branches with needles | 492.00 ± 52.16 1 | 390 | 576 | 2720.22 | -0.46 | |
Shrub | Frangula alnus | branches with leaves | 238.00 ± 31.30 2, 8 | 188 | 292 | 979.78 | -0.07 | |
Herb | Pteridium aquilinum | leaves | 794.00 ± 83.50 3, 9, 14, | 665 | 942 | 6972.89 | 0.14 | |
Dwarf shrub | Vaccinium myrtillus | shoots | 487.00 ± 75.75 4, 10, 15, 19 | 378 | 592 | 5739.33 | -0.02 | |
Dwarf shrub | Calluna vulgaris | shoots | 589.00 ± 88.26 5, 11, 16, 23 | 467 | 751 | 7789.56 | 0.41 | |
Mosses | Pleurozium schreberi | caulidia with philidia | 814.00 ± 69.38 6, 12, 17, 21, 24, 26 | 730 | 970 | 4814.00 | 0.71 | |
Mosses | Ptilium crista-castrensis | caulidia with philidia | 822.00 ± 92.10 7, 13, 18, 22, 25, 27, 28 | 675 | 964 | 8481.78 | -0.38 |
The comparative analysis showed that the highest 137Cs specific activity was recorded in the Frangula alnus plant samples in plot 3, with a mean value of 352.00 ± 40.07 Bq kg-1 (Tab. 3). This value exceeds the maximum permissible specific activity (MPSA) by 76% (Fig. 3). It should be noted that the 137Cs MPSA for vegetable raw materials is 200 Bq kg-1 ([24]).
Fig. 3 - The mean values of 137Cs relative specific activity (%) in plant samples compared to maximum permissible specific activity (MPSA); 1 - Betula pendula, 2 - Pinus sylvestris, 3 - Frangula alnus, 4 - Pteridium aquilinum, 5 - Vaccinium myrtillus, 6 - Calluna vulgaris, 7 - Pleurozium schreberi, 8 -Ptilium crista-castrensis.
Radiostrontium (90Sr) exhibited a higher bioaccumulation in plant tissues than 137Cs. This confirms the findings obtained by previous studies showing that pharmaceutical tree and shrub plants exhibited much stronger accumulation of strontium than cesium ([19]). The comparative analysis showed the highest value of 90Sr accumulation in the vegetative organs of Pteridium aquilinum and mosses in the experimental plots 1 and 2 (Tab. 1, Tab. 2). The highest 90Sr specific activity was recorded in the Pteridium aquilinum plant samples in plot 2 (2860.00 ± 378.49 Bq kg-1 - Tab. 2). The 90Sr MPSA threshold for vegetable raw materials is 500 Bq kg-1 ([24]). The highest excess of the 90Sr MPSA was observed in Pteridium aquilinum from plot 2, equalling 372% of the threshold (Fig. 4). In the herb layer, the excess of 137Cs MPSA in the leaves of the co-dominant fern Pteridium aquilinum was estimated to be between 7.5% and 21.5% across samples from all plots.
Fig. 4 - The mean values of 90Sr relative specific activity (%) in plant samples compared to maximum permissible specific activity (MPSA, in green); 1 - Betula pendula, 2 - Pinus sylvestris, 3 - Frangula alnus, 4 - Pteridium aquilinum, 5 - Vaccinium myrtillus, 6 - Calluna vulgaris, 7 - Pleurozium schreberi, 8 -Ptilium crista-castrensis.
The lowest 90Sr specific activity (212.00 ± 26.15 Bq kg-1) was recorded in the Frangula alnus branches with leaves in plot 3 (Tab. 3). It should be noted that 90Sr specific activity of 39.4 Bq kg-1 was observed in Frangula alnus cortex from the Lublin (Poland) region ([19]). For comparison, this is more than 10 times less than the 90Sr specific activity in Viola tricolor L. flowers collected in this region. The high bioaccumulation of radionuclides detected for Frangula alnus might be a species-specific characteristic, but further studies are needed to confirm this result.
The tree layer dominants (Pinus sylvestris and Betula pendula) were minimally contaminated with radiostrontium. A slight excess (2%) of the 90Sr MPSA was found in plot 2 in the Pinus sylvestris branches with needles. The deviation (62%-73.4%) from the 90Sr MPSA (Fig. 4) is smaller in the Vaccinium myrtillus shoots compared to the Calluna vulgaris shoots. Schmidt et al. ([18]) carried out a study on the radionuclide accumulation in Bryophytes in the Chernobyl Exclusion Zone, showing that the 90Sr uptake behaviour in mosses is counterintuitive and not affected by the presence or lack of vascular tissue. In this study, we obtained similar values of 90Sr specific activity in both moss species (Pleurozium schreberi and Ptilium crista-castrensis) within the same experimental plot for all the plots. In Bryophytes, an excess of the 90Sr MPSA in the range of 56%-328% was observed in all the plots (Fig. 4).
Both 90Sr and 137Cs are readily absorbed by plant leaves. However, 137Cs is more likely translocated into fruits and seeds compared to 90Sr, which tends to remain in the plant part where it was initially absorbed. The uptake of these radionuclides from soil to root is conditioned by soil chemical and physical factors, which may selectively retain a radionuclide, such as 137Cs. The presence of organic matter, inorganic colloids (clay), and competing elements can strongly affect the uptake of radiostrontium and radiocesium by plants from the soil.
MANOVA analysis
The results of MANOVA showed significant differences in the 137Cs/90Sr ratio among the different layer levels, plant species, and plant parts among the specified forest areas.
In the case of the 137Cs bioaccumulation, the MANOVA yielded a significant F-ratio (F[4, 315] = 172.64, p<0.001), indicating that the relationship between the dependent variable (137Cs accumulation) and the predictors (area type, layer level, plant species, and plant part) is highly significant. Moreover, the MANOVA results revealed a high multiple correlation coefficient (R = 0.829), which indicates that approximately 82.87% of the variance in the dependent variable can be explained by the combination of the predictor variables. The coefficient of determination R2 was approximately 68.67%; however, after correction of the degrees of freedom for the number of predictors and sample size, the adjusted R2 value was 0.683, i.e., 68.28% of the total variance was explained by the combination of predictor variables.
Regarding 90Sr bioaccumulation, the results yielded a significant F-ratio (F[4, 315] = 30.607, p<0.001), indicating a significant relationship between the predictors and the dependent variable. The multiple correlation coefficient (R) was 0.529, while the coefficient of determination R2 was 0.279 and the adjusted R2 was 0.271, suggesting that approximately 27.1% of the variance in the dependent variable can be explained by the combination of predictors.
The beta coefficients of the regression analysis indicated the magnitude and direction of the effect of the different predictor variables (area type, layer level, plant species, and plant part) on radionuclide accumulation. In the case of 137Cs, the layer level (β = 2.601 ± 0.159, p < 0.001), the plant species (β = -0.429 ± 0.151, p = 0.005) and the plant part (β = -2.456 ± 0.101, p < 0.001) showed a significant impact on the accumulation of radiocesium in the studied forest biocoenoses. Regarding the 90Sr bioaccumulation, the only significant coefficient was found for the area type (β = -0.425 ± 0.048, p < 0.001).
Both 137Cs and 90Sr are influenced by plot type, but in a different way. For 90Sr, the negative beta coefficient implies that lower 90Sr accumulation are associated to certain area types (=sites). While significant, the effect of area type for 137Cs suggests that plot characteristics may affect 137Cs bioaccumulation in a more complex way. These contrasting results also suggest that 137Cs accumulation is more sensitive to changes in the stratum level compared to 90Sr. This could be due to differences in the environmental migration of these radionuclides, their chemical properties, differences in soil-plant transfer mechanisms or how each radionuclide interacts with different forest layers. The significant effect of plant species on 137Cs/90Sr accumulation highlights the role of plant-specific characteristics in influencing radionuclide uptake. The significant variation in 137Cs/90Sr accumulation between different plant parts suggests that certain plant parts accumulate more 137Cs than others.
The results of MANOVA indicate a higher accumulation of 137Cs compared to 90Sr. The R2 values and the F-tests indicate a significant and strong relationship between the independent and dependent variables. Hence, it can be hypothesized that the processes of accumulation and dispersion of 137Cs are more complex in the studied areas and among plant layers than those of 90Sr. Further research on the mechanisms of accumulation and distribution of these radionuclides may be essential for a better understanding of their impact on the environment and human health.
Discussion
Our study examines the differences in the accumulation of specific radionuclides and their ratios across various soil layers, plant species, and plant parts within birch-pine forest communities near the Chernobyl Exclusion Zone, specifically the Bleshnya and Orlykivka forests of the Semenivka State Forestry in the Chernihiv Region of Northern Ukraine. This study explores the dynamics of radionuclide accumulation in forest ecosystems following the Chernobyl disaster, which is crucial for assessing current environmental risks and developing effective management strategies. Additionally, our research enhances the understanding of radionuclide dynamics in these ecosystems, providing valuable insights into ecological responses to radioactive contamination and guiding future research and environmental management efforts. Ultimately, our results contribute to a better understanding of the patterns of 137Cs and 90Sr radionuclide accumulation in the birch-pine forest communities of the Chernihiv region in Ukraine.
We found the lowest 137Cs specific activity in the Pinus sylvestris plant samples in plot 3 with a mean value of 73.00 ± 8.25 Bq kg-1 (Tab. 3). The Pinus sylvestris branches with needles from all the plots did not exceed the radiocesium MPSA threshold. The Betula pendula branches with leaves from the third and fourth plots had a slight 2% and 6% MPSA excess, respectively (Fig. 4). These results are in good agreement with findings from Eastern Poland ([22]), which indicate that higher levels of 137Cs accumulate in birch (Betula pendula) than in pine (Pinus sylvestris). This is also confirmed by the transfer coefficients of the 137Cs isotope, which were higher in birch wood than in pine wood, especially in older stands. Indeed, as the age of the stand increases, the accumulation of 137Cs in wood has been also found to increase ([22]).
As for the herb layer, in the leaves of the co-dominant fern Pteridium aquilinum, the 137Cs excess was estimated to be 7.5%-21.5% higher than MPSA level in the samples from all the plots. The significant accumulation of 137Cs in ferns has been previously reported in the scientific literature. Calmon et al. ([3]) found that the aggregated transfer factors for vascular plants growing in forests on mineral soils were generally lower than in a peat-land forest or in plants growing on a thick organic soil layer. Both perennial and annual plants differed in the uptake of 137Cs. The highest values were found for the fern Dryopteris carthusiana (Vill.) H.P.Fuchs ([3]) in an ecosystem similar to the forest ecosystems considered in this study.
Notably, isolated cases of MPSA excess for 137Cs were found in the moss and dwarf shrub layers. For example, the dominant species Calluna vulgaris and Pleurozium schreberi exhibited an excess of the radiocesium only in the samples from plot 1 (11.5% higher than the MPSA threshold). It is known that mosses accumulate pollutants from precipitation and, to a lesser extent, from the substrate ([21]). The vegetative organs of Vaccinium myrtillus had a moderate degree of 137Cs accumulation. Following the Chernobyl accident, the 137Cs content in all plant organs across various berry species demonstrated a clear decreasing trend. Long-term monitoring data after the Chernobyl accident ([3]) indicated a relatively rapid decline in the 137Cs specific activity in both the aboveground biomass and in the berries of the main berry species in the initial period following deposition (1986-1995). However, this decrease slowed significantly in the years following 1995.
It is well-established that mosses absorb radioisotopes from the environment differently than higher plants due to their unique structural features. This difference occurs both in the quantity and quality of uptake. Moreover, mosses are likely to display a wide range of uptake patterns influenced by their anatomy, the availability of radioisotopes on the surface layer of their substrate - such as soil, rock, or tree bark - as well as from unusual substrates like animal corpses or hairballs. Dust deposition may also play a role in determining these patterns ([18]). A study on 137Cs in Bryophytes found pronounced differences between samples but no conclusive evidence for differences between taxa ([4]). Our research confirms the above evidence for Bryophytes in plots 2 and 3 (Tab. 2, Tab. 3). In plot 1, both the lowest and the higher average values of the radiocesium-specific activity (32.00 ± 15.48 and 223.00 ± 30.70 Bq kg-1 in Ptilium crista-castrensis and Pleurozium schreberi, respectively) were recorded in Bryophytes.
This study combined field research methods with laboratory analysis techniques, including gamma spectrometry and radiochemical methods. This methodological approach represents an advancement in assessing radionuclide accumulation in plant samples as it considers plants to be effective indicators for monitoring the environmental conditions. Plants can absorb radionuclides through their leaves and shoots from the air or from the soil via their roots. The epidermal characteristics of plant foliage may affect particle retention on leaves and the subsequent uptake of radionuclides from the surface. The transport of radionuclides through the cuticle and epidermis of leaves is affected by leaf anatomy and physiological factors, which can largely differ across different species. Moreover, evidence of long-term deposit of radionuclides in the soil has been reported.
Our results indicated that different species respond uniquely to radionuclide uptake. For example, the fern Pteridium aquilinum exhibited an outstanding level of bioaccumulation in this study. This highlights the need to consider species-specific responses when dealing with radioactive contamination. Understanding these differences is crucial for creating targeted mitigation strategies and evaluating ecological risks.
In our study, we observed variations in the accumulation of the radionuclides 137Cs and 90Sr among different plant species. These differences can be attributed to several factors, including variations in root morphology and depth, differences in uptake mechanisms, variations in metabolic processes, or species-specific affinity for these radionuclides. Environmental factors, such as soil composition, pH levels, and the availability of nutrients, also play a significant role in influencing how plants uptake and accumulate radionuclides. Understanding the complex interplay of these factors is essential for a comprehensive understanding of the variations in radionuclide accumulation among different plant species.
The accumulation of 137Cs and 90Sr in various forests of Ukraine following the Chernobyl disaster differs significantly. These differences can be attributed to several factors, including differences in soil composition, vegetation types, and environmental conditions across the affected regions. Additionally, the intensity of radioactive fallout and subsequent remediation efforts may vary from one forest to another, leading to differences in radionuclide accumulation levels. Understanding these variations is crucial for assessing the long-term environmental impact of the nuclear disasters and implementing targeted management strategies to mitigate further contamination.
In this study, we showed that 90Sr had greater accumulation than 137Cs in birch-Scots pine forest ecosystems. These findings offer important insights into the dynamics of radionuclide bioavailability, which is essential for predicting their fate and transport in terrestrial environments. Understanding the mechanisms driving the retention, translocation, and bioaccumulation of radioactive contaminants, can help develop targeted approaches for monitoring and remediating contaminated areas, thereby mitigating potential threats to both human health and the environment ([12], [17], [2], [27], [18]).
The insights gained from studying the Chernobyl-affected forests should serve as a benchmark for similar environments worldwide, informing global efforts in nuclear safety, environmental protection, and sustainable land management practices.
Conclusions
Our study helps understand how 137Cs is absorbed by plants and how its presence affects the birch-Scots pine forest ecosystems in Ukraine. We found variations in the accumulation of the 137Cs and 90Sr radionuclides among different plant species. The MANOVA regression analysis revealed significant relationships in radionuclide accumulation across different layer levels, plant species, and plant parts in the studied forest areas. The analysis showed that 90Sr accumulation is lower in certain area types, while the effect of area type on 137Cs is more variable. 137Cs accumulation is more sensitive to layer-level changes compared to 90Sr, probably due to differences in environmental behavior, chemical properties, or soil-plant transfer mechanisms. Plant species significantly differed in 137Cs/90Sr ratio, and several parts of plants showed more 137Cs bioaccumulation than others. These differences may be attributed to various factors, such as root structure, uptake mechanisms, or specific physiological characteristics of each plant species.
Further research is needed to elucidate the underlying mechanisms driving these variations and their implications for ecosystem dynamics and environmental management. Continued research in this field is essential for better understanding the long-term effects of radioactive contamination.
Acknowledgments
The Ministry of Education and Science of Ukraine has financed this research.
References
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Authors’ Info
Authors’ Affiliation
Oleksandr Yakovenko 0000-0003-1417-6042
Department of Ecology, Geography and Nature Management, T.H. Shevchenko National University “Chernihiv Colehium”, Chernihiv (Ukraine)
Natalia Kurhaluk 0000-0002-4669-1092
Institute of Biology, Pomeranian University in Slupsk, Slupsk (Poland)
Department of Biology and Chemistry, Ferenc Rákóczi II Transcarpathian Hungarian College of Higher Education, Berehove (Ukraine)
Corresponding author
Paper Info
Citation
Lukash O, Tkaczenko H, Yakovenko O, Szikura A, Kurhaluk N (2024). Accumulation of 137Cs and 90Sr radionuclides by dominants and co-dominants of birch-pine forest communities in Northern Ukraine. iForest 17: 386-393. - doi: 10.3832/ifor4577-017
Academic Editor
Rossella Guerrieri
Paper history
Received: Feb 06, 2024
Accepted: Sep 22, 2024
First online: Dec 20, 2024
Publication Date: Dec 31, 2024
Publication Time: 2.97 months
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© SISEF - The Italian Society of Silviculture and Forest Ecology 2024
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