Distribution Of 137Cs Research Articles

Modeling of <sup>137</sup>Cs Dispersion in the Atlantic Ocean at Ahanta West Coast: A Hypothetical Candidate Site for Ghana’s First Nuclear Power Plant

The government of Ghana has the intention of adding nuclear to its energy mix. Due to water availability for cooling, the coastal areas will be the right place for siting a nuclear power plant. This study was carried out to assess the distribution of 137Cs should liquid radioactive waste be released into coastal waters because of a non-routine event. The distribution was studied for the first month after the release. In the first week following the release, 137Cs was distributed within 16 km of the Ahanta West coastal waters with a concentration of about 9.1 Bq. L-1. On the seventh day, the distribution reached the entire coast of the Nzema East with a lower concentration with the bulk of the concentration still in the Ahanta waters. The 137Cs continued to spread into the eastern coast until the thirty-first day with a concentration of less than 1 Bq. L-1. This study provides useful data for future monitoring along the coast.

High-energy SR-XRF Imaging of Cesium and Trace Elements in Mouse Kidneys: Short Communication.

For understanding trace element dynamics in tissues, methods for analyzing elemental distribution and localization without destroying tissue structures and cell arrangements are desired. Synchrotron radiation X-ray fluorescence (SR-XRF) analysis is one of the non-destructive and multi-element simultaneous analyses. The kidney is the major excretion pathway of cesium (Cs) taken into the body, and an understanding of cesium distribution in the kidney would be useful for establishing technology to facilitate the excretion of radioactive Cs from the body due to nuclear disasters. In the present study, the distribution of cesium and trace elements, such as iron (Fe) and zinc (Zn), corresponding to the kidney structure was examined in Cs-administered mice by SR-XRF imaging with high-energy excitation X-rays (40keV). By beam scanning with a 200-µm square beam, clear Cs images corresponding to the renal layer structure were obtained for the renal specimen at the early phase after Cs administration with the mean renal Cs concentration of 24.1 ± 3.2μg/g. Cs was distributed mainly in the medulla and the outer stripe of the outer medulla located in the center area of the kidney. Unlike the Cs distribution, endogenous Fe and Zn tended to be lower in the medulla than in the outer stripe of the outer medulla and the cortex. This method is effective for analyzing Cs distribution because it can simultaneously analyze the distribution of endogenous trace elements.

Two‐stage soil core sampler to collect a less‐compressed core from forested areas

AbstractA two‐stage sampler was designed to investigate the vertical distribution of heavy metals and trace elements that contaminate forest soils through atmospheric deposition. The hand‐corer consisted of two L‐shaped aluminum angles that were driven separately into the soil to reduce friction between the corer wall and the soil. This allowed for soil cores to be collected with less compression than with traditional corers. The corer is easily made, inexpensive, lightweight, and easy to carry. The degree of compression of soil cores collected at a depth of 20 cm from various montane forests in Japan was usually less than 10% (collected core length >18 cm); although, more compression occurred in soil with a higher air content. The degree of compression of soil cores collected from urban forests was lower than that in montane forests. When the two‐stage sampler was compared with a tube‐type sampler in a Japanese cedar (Cryptomeria japonica) forest, the compression degree of a soil core collected with the two‐stage sampler was a quarter that of the tube‐type sampler. The collection of less‐compressed soil cores will allow for reconstruction of a more accurate linear depth distribution of contaminants. To demonstrate this, we investigated the vertical distribution of Pb, Sb, and radioactive 137Cs in soil cores collected from conifer plantations on Mount Tsukuba, Japan, in April 2011. The migration centers of anthropogenic Pb, Sb, and 137Cs were positioned at 7.9, 7.5, and 3.3 cm from the ground surface, respectively. These distances probably reflect differences in the history of atmospheric pollution.

Confirmation of the recognition of Culiseta (Culiseta) indica Edwards, 1920 as a distinct species based on integrated morphological and molecular data.

Theobaldia indica Edwards, 1920, classified as a subspecies of Culiseta (Culiseta) alaskaensis (Ludlow, 1906), was recently restored to its original species status, as Culiseta (Culiseta) indica (Edwards), based on comprehensive assessments of morphological, ecological and distributional data. Predating the recognition of indica as a separate species, we collected specimens of this nominal taxon in the Western Himalayan region of India during 20152017, and used morphological and molecular studies to assess its taxonomic status. Our detailed examination of adult morphology, male genitalia and larval characteristics revealed significant distinctions between putative Cs. alaskaensis alaskaensis and Cs. alaskaensis indica, and sequencing of the barcode region of the mitochondrial COI gene yielded a Kimura 2 parameter genetic distance of 5.9% between them, well above the standard 23% commonly accepted to indicate separate species. These results strongly support the formal recognition of Cs. indica as a separate species. Furthermore, the geographical distribution of Cs. indica provides additional evidence in support of its species status.

Глобальное загрязнение территории Южной Якутии Cs-137 и дозы облучения населения

The aim of the work is to estimate the radioactivity of Cs-137 in the soils of South Yakutia and to calculate the dose of internal irradiation of a critical group of people caused by the consumption of local foods containing radionuclide. An assessment of the radioactive contamination of the soil cover of South Yakutia showed that the radioactivity of Cs-137 in the soils of eluvial landscapes varies between 714 and 1,665 Bq/m2 and is commensurate with the radioactivity of Cs-137 in the soils of the Primorsky Krai, the Western Siberia and the Kola Peninsula. The present soil contamination levels of Cs-137, compared to the 2003 data, have been reduced on average by half due to radioactive decay of the radionuclide, the soil deepening and removal with surface water and vegetation. At present time there is no appreciable additional input of Cs-137 from the atmosphere to the soil cover of automorphic taiga landscapes in the South Yakutia. The specific activity of Cs-137 in watershed soils and river floodplains is low and corresponds to the background level of global pollution. The vertical distribution of Cs-137 over the soil profile of eluvial landscapes is realized on regressive-cumulative and eluvial-illuvial types. In soil profiles of hydromorphic landscapes Cs-137 is distributed, without any clear patterns, which is a consequence of the impact of alluvial processes. Calculations showed that at the current level of contamination of local foodstuffs, the annual effective dose of internal exposure of a critical population group from this radionuclide is 87 times less than the annual dose limit for the Russian population.

The migration behavior of cesium during plasma gasification melting process of spent radioactive resins by thermodynamic calculation

Plasma gasification melting is an effective method of spent radioactive resin disposal. However, the equilibrium distribution and migration of Cs during the plasma gasification melting process is still unclear. In this study, the volatilization behavior of Cs during the plasma gasification melting process of spent resins was investigated by thermodynamic model. The composition of the stable phase and the release of Cs from the stable phase in the three systems of Cs-C-O, Cs-S-O and Cs-N-O were calculated by HSC Chemistry. The possible composition of Cs during the plasma gasification melting process of spent resins was determined. At the same time, the thermodynamic simulation of spent resins in the temperature range of 300–1800 °C was carried out, and the morphological distribution of Cs during the plasma gasification melting process of spent resins was calculated and analyzed, which will provide theoretical guidance for subsequent experimental research. The results showed that Cs2CO3, Cs2SO4 and Cs2O were identified as the stable phases of each system at 1200 °C in air atmosphere. The existent forms of Cs in the three stages of plasma pyrolysis, gasification and melting are different. In the plasma pyrolysis and melting stage, Cs mainly enters the gas phase in the form of gaseous Cs and CsOH. In the plasma gasification stage, Cs mainly enters the gas phase in the form of gaseous Cs and Cs2SO4. By comparing with the results of some literature, the accuracy of thermodynamic calculation is proved. The migration and transformation law of Cs during the plasma gasification melting process of spent radioactive resins is revealed.

<sup>137</sup>Cs migration and pro le in bottom sediments of deep drainage lakes, north-western Russia

Modern contamination of global and «Chernobyl» 137Cs in lake-river systems bottom sediments is estimated. Drainage lakes of North-Western Russia were investigated. Kopanskoe Lake, located south of the Gulf of Finland, is on the trail of the «Chernobyl» 137Cs fallout, whereas Ladoga, Sukhodolskoe, Vuoksa, Imandra lakes are located at its periphery, in Karelia and Kola Peninsula. Following parameters are distinguished: lakes bottom 137Cs pollution density (kBq/m2), distribution of 137Cs in the pro le of bottom sediments, 137Cs di usion coe cients ( D ) in bottom sediments and content of the exchange chemical form of the radionuclide. 137Cs contamination of the lakes was formed due to suspended matter sedimentation with 137Cs, 137Cs sorption and di usion in bottom sediments. With sedimentation ≥3 mm/year, the concentration of 137Cs increased from the top to the bottom of the core (lakes Vuoksa, Ekostrovskaya Imandra), re ecting the gradual process of 137Cs migration into the sediments. The opposite trend of 137Cs concentration was observed in the bottom sediments of lakes Ladoga and Sukhodolskoe with sedimentation ≤0.5 mm/year. Here 137Cs di usion with D = (0.5-6.2) ×10-8 cm2/s caused slow radionuclide transfer in the bottom sediments. The main supply of 137Cs was contained in the top layer 0-5 cm. 14.4-20 % of absorbed 137Cs in lake Sukhodolskoye bottom sediments were was in an exchange chemical form, extracted into solution 1 М NH 4 Aс.

Relationship between stable cesium concentration and body size of Japanese flounder Paralichthys olivaceus and the effect of a size-dependent shift in diet.

To understand the relationship between the radioactive cesium (Cs) concentration in muscle of Japanese flounder Paralichthys olivaceus and the species' biological characteristics (size, sex, and age) under conditions of ecological equilibrium (i.e., distributed among ecosystem components over sufficient time, and with nearly constant ratios of Cs concentration in organisms to the concentration in water) as existed before the accident at the Fukushima Dai-ichi Nuclear Power Station (FDNPS), Japan, in 2011, we examined stable Cs, as it is thought to exist in equilibrium in the environment and behave similarly to radioactive Cs in aquatic animals. The concentration of stable Cs in 241 P. olivaceus (range 216-782 mm total length [TL]) collected in Sendai Bay, approximately 90 km north of the FDNPS, in June-July 2015 was expressed as an exponential function with size as an independent variable; the results show the concentration of stable Cs doubled with an increase in TL of 442 mm. Next, to evaluate the cause of the size-dependent change in stable Cs concentration, we examined 909 individuals (200-770 mm TL) collected in September 2013-July 2015 to determine their feeding habit based on size. Analysis of the frequency of occurrence of prey organisms in stomach contents showed that sand lance Ammodytes japonicus (55-180 mm standard length [SL]) was the most consistently consumed across size classes. Analysis on a wet-mass basis showed that A. japonicus and anchovy Engraulis japonicus (65-130 mm SL) were the main food of P. olivaceus sized 200-599 mm TL, whereas chub mackerel Scomber japonicus (120-230 mm SL) and two species of flatfishes (180-205 mm SL) were abundant in the diet of P. olivaceus sized ≥600 mm TL. All these prey items were presumed to have similar concentrations of stable Cs. Based on the above, the effect of diet on the relationship between stable Cs in muscle and fish size was considered negligible. That the diet of P. olivaceus largely did not change with size was also confirmed by C and N stable isotope ratios in P. olivaceus and their prey species. Therefore, the Cs-size relationship is probably determined by changes in the balance between the rate of Cs intake from food and seawater and the excretion rate during growth, both of which change as functions of body mass. Values of stable Cs concentrations among environmental components and animals appear to be a valid indicator for understanding the radioactive Cs distribution in the marine environment and aquatic animals under the equilibrium state, as existed before the 2011 nuclear accident.

Leveraging the Proximity and Distribution of Cu−Cs Sites for Direct Conversion of Methanol to Esters/Aldehydes

AbstractMethanol serves as a versatile building‐block for various commodity chemicals, and the development of industrially promising strategies for its conversion remains the ultimate goal in methanol chemistry. In this study, we design a dual Cu−Cs catalytic system that enables a one‐step direct conversion of methanol and methyl acetate/ethanol into high value‐added esters/aldehydes, with customized chain length and saturation by leveraging the proximity and distribution of Cu−Cs sites. Cu−Cs at a millimeter‐scale intimacy triggers methanol dehydrogenation and condensation, involving proton transfer, aldol formation, and aldol condensation, to obtain unsaturated esters and aldehydes with selectivities of 76.3 % and 31.1 %, respectively. Cu−Cs at a micrometer‐scale intimacy significantly promotes mass transfer of intermediates across catalyst interfaces and their subsequent hydrogenation to saturated esters and aldehydes with selectivities of 67.6 % and 93.1 %, respectively. Conversely, Cu−Cs at a nanometer‐scale intimacy alters reaction pathway with a similar energy barrier for the rate‐determining step, but blocks the acidic‐basic sites and diverts the reaction to byproducts. More importantly, an unprecedented quadruple tandem catalytic production of methyl methacrylate (MMA) is achieved by further tailoring Cu and Cs distribution across the reaction bed in the configuration of Cu−Cs||Cs, outperforming the existing industrial processes and saving at least 15 % of production costs.

Leveraging the Proximity and Distribution of Cu-Cs Sites for Direct Conversion of Methanol to Esters/Aldehydes.

Methanol serves as a versatile building-block for various commodity chemicals, and the development of industrially promising strategies for its conversion remains the ultimate goal in methanol chemistry. In this study, we design a dual Cu-Cs catalytic system that enables a one-step direct conversion of methanol and methyl acetate/ethanol into high value-added esters/aldehydes, with customized chain length and saturation by leveraging the proximity and distribution of Cu-Cs sites. Cu-Cs at a millimeter-scale intimacy triggers methanol dehydrogenation and condensation, involving proton transfer, aldol formation, and aldol condensation, to obtain unsaturated esters and aldehydes with selectivities of 76.3 % and 31.1 %, respectively. Cu-Cs at a micrometer-scale intimacy significantly promotes mass transfer of intermediates across catalyst interfaces and their subsequent hydrogenation to saturated esters and aldehydes with selectivities of 67.6 % and 93.1 %, respectively. Conversely, Cu-Cs at a nanometer-scale intimacy alters reaction pathway with a similar energy barrier for the rate-determining step, but blocks the acidic-basic sites and diverts the reaction to byproducts. More importantly, an unprecedented quadruple tandem catalytic production of methyl methacrylate (MMA) is achieved by further tailoring Cu and Cs distribution across the reaction bed in the configuration of Cu-Cs||Cs, outperforming the existing industrial processes and saving at least 15 % of production costs.

Distribution of 137Cs in the marine environment from King George Island (Southern Shetlands, maritime Antarctica)

The article presents data on the activity of the radionuclide 137Cs in seawater, sediment, macroalgae, and zoobenthos from different locations in Admiralty Bay, King George Island, maritime Antarctica. The activity of 137Cs in the macrophytobenthos remained relatively stable across species, oscillating at the level of 1 Bq kg−1dw. However, a few individuals exhibited higher activity, particularly at stations closer to the glacier front. This result could have been caused by specific conditions resulting from melting glaciers and meltwater inflow and mixing with oceanic water. The activities of 137Cs in zoobenthic were in the range from 0.12 Bq kg−1dw (Asteroidea) to 24.2 Bq kg−1dw (Porifera) and the total doses in marine species were several orders of magnitude lower than reference levels. Stable isotopes of δ13C and δ15N suggest that the main factor influencing 137Cs activity may be the source of carbon (marine vs. terrestrial/glacial), rather than feeding strategy or trophic niches.

Simulated inventory and distribution of 137Cs released from multiple sources in the global ocean

Radioactive cesium (137Cs) is distributed in the world's oceans as a result of global fallout from atmospheric nuclear weapons tests, releases from fuel reprocessing plants, and inputs from nuclear power plant accident. In order to detect future radionuclide contamination, it is necessary to establish a baseline global distribution of radionuclides such as 137Cs and to understand the ocean transport processes that lead to that distribution. In order to aid in the interpretation of the observed database, we have conducted a suite of simulations of the distribution of 137Cs using a global ocean general circulation model (OGCM). Simulated 137Cs radioactivity concentrations agree well with observations, and the results were used to estimate the changes in inventories for each ocean basin. 137Cs activity concentration from atmospheric nuclear weapons tests are expected to be detectable in the world ocean until at least 2030.

Colloidal CsBr Nanocrystals Triggered Inorganic Cation and Anion Exchange Enables High-Performance Perovskite Solar Cells.

Achieving longitudinal doping of specific ions by surface treatment remains a challenge for perovskite solar cells, which are often limited by dopant and solvent compatibility. Here, with the flowing environment created by CsBr colloidal nanocrystals, ion exchange is induced on the surface of the perovskite film to enable the homogeneous distribution of Cs+ and gradient distribution of Br- simultaneously at whole depth of the film. Meanwhile, assisted by long-chain organic ligands, the excess PbI2 on the surface of perovskite film is converted to a more stable quasi-2D perovskite, which realizes effective passivation of defects on the surface. As a result, the unfavorable n-type doping on the top surface is suppressed, so that the energy level alignment between perovskite and hole transport layer is optimized. On the basis of co-modification of the surface and the bulk, the PCE of champion device reaches 23.22% with enhanced VOC of 1.12V. Device maintains 97.12% of the initial PCE in dark ambient air at 1% RH after 1056h without encapsulation, and 91.56% of the initial PCE under light illumination of 1 sun in N2 atmosphere for more than200h. The approach demonstrated here provides an effective strategy for the nondestructive introduction of inorganic ions in perovskite film.

Modeling long-term transfers of radiocesium in farmland under different tillage and cover crop treatments

The 2011 nuclear accident at Japan's Fukushima Daiichi Nuclear Power Plant (FDNPP) prompted inquiries about the long-term transfer of Cesium-137 (137Cs) from soil to agricultural plants. In this context, numerical modeling is particularly useful for the long-term evaluation of the consequences of agroecosystem contamination. Agricultural practices, such as tillage and cover cropping, play key roles in 137Cs recycling in agroecosystems. In this study, we used 10-year monitoring data to develop a dynamic model to predict 137Cs redistribution (via uptake, litterfall, translocation, and percolation) under different tillage (no-tillage, NT; rotary cultivation, RC; moldboard plow, MP) and cover crop (rye; hairy vetch; fallow weed) treatments. The verification exercise and assessment results indicated the model's reliability, as the temporal dynamics of predicted values agreed with observed values. Tillage significantly influenced the 137Cs distribution in soil, thereby decreasing plant uptake of 137Cs, whereas cover crop exerted a minimal effect on 137Cs cycling. Furthermore, while the 137Cs concentrations in soybean grain under RC and NT treatments were comparable 62 years after the FDNPP accident, the concentration under MP treatment remained consistently the lowest. Despite natural decay being the main cause of the decreased global 137Cs level in the agroecosystem, with minimal losses from percolation to deeper soil layers and soybean harvesting, adopting an appropriate tillage practice was shown to promote a long-term reduction of 137Cs concentration in crops. Finally, to improve the model's accuracy, further research should consider incorporating the effects of soil properties and extreme weather events on 137Cs flow into the model, as these factors are essential for realizing improved agroecosystem predictions.

Моделирование нисходящего переноса 210Pb на примере естественного торфяника Иласского болотного массива Европейской Субарктики России: модель IP-CRS

The paper presents the results of the modelling of the transport of 210Pb down the peat core for the Ilassky natural bog massif. The activities of radionuclides 210Pb and 137Cs were investigated in the core layer by layer. Due to the nonexponential decrease of 210Pb activity, significant errors are possible in determining the age and accumulation rates of peat when applying classical dating models. The article presents 210Pb dating data obtained using the IP-CRS model. Data analysis showed that the vertical distribution of 137Cs and 210Pb is related to peat parameters: ash content and bulk density. The 210Pb dating of the core showed an age of 1963 for a depth of 17—19 cm, which is consistent with the 137Cs data. The dating of this horizon is indirectly confirmed by the data of the ash content and bulk density of peat. The above mentioned confirms the correctness and adequacy of the chosen model of dating of the natural peat bog. The peak of anthropogenic radionuclide content in peat deposits corresponds to 1963, the date of signing the Partial Nuclear Test Ban Treaty, being a reference point for geochronological studies. The results of linear accumulation rate, peat deposit mass accumulation rate and the magnitude of the atmospheric flux of 210Pb presented in the study are in good agreement with the data on peatlands of Northern Europe and the European Subarctic of Russia.

Xylem K+ loading modulates K+ and Cs+ absorption and distribution in Arabidopsis under K+-limited conditions.

Potassium (K+) is an essential macronutrient for plant growth. The transcriptional regulation of K+ transporter genes is one of the key mechanisms by which plants respond to K+ deficiency. Among the HAK/KUP/KT transporter family, HAK5, a high-affinity K+ transporter, is essential for root K+ uptake under low external K+ conditions. HAK5 expression in the root is highly induced by low external K+ concentration. While the molecular mechanisms of HAK5 regulation have been extensively studied, it remains unclear how plants sense and coordinates K+ uptake and translocation in response to changing environmental conditions. Using skor mutants, which have a defect in root-to-shoot K+ translocation, we have been able to determine how the internal K+ status affects the expression of HAK5. In skor mutant roots, under K+ deficiency, HAK5 expression was lower than in wild-type although the K+ concentration in roots was not significantly different. These results reveal that HAK5 is not only regulated by external K+ conditions but it is also regulated by internal K+ levels, which is in agreement with recent findings. Additionally, HAK5 plays a major role in the uptake of Cs+ in roots. Therefore, studying Cs+ in roots and having more detailed information about its uptake and translocation in the plant would be valuable. Radioactive tracing experiments revealed not only a reduction in the uptake of 137Cs+ and 42K+in skor mutants compared to wild-type but also a different distribution of 137Cs+ and 42K+ in tissues. In order to gain insight into the translocation, accumulation, and repartitioning of both K+ and Cs+ in plants, long-term treatment and split root experiments were conducted with the stable isotopes 133Cs+ and 85Rb+. Finally, our findings show that the K+ distribution in plant tissues regulates root uptake of K+ and Cs+ similarly, depending on HAK5; however, the translocation and accumulation of the two elements are different.

The transfer of 137Cs and heavy metals to tissues within the organs of snails

This paper describes the dynamics of 137Cs accumulation and its concentration ratio as well as that of some stable elements in the body, shell, gastrointestinal tract and albumin gland of a particular species of snail (terrestrial gastropod), namely the Giant African snail (Lissachatina fulica), after the long-term ingestion of contaminated forage and/or soil. The activity concentration of 137Cs in the their bodies increased over the first 40 days of the experiment, after which the increase in the activity of this radionuclide significantly reduced. The distribution of 137Cs in the body of a snail decreases as follows: gastrointestinal tract ˃ body = albumin gland ˃ shell. It was found that the contribution of soil towards the contamination of their bodies by 137Cs is far less than that of forage. Although the biological availability of Pb and U in forage is one order of magnitude higher than in soil, the main contribution to the contamination of snails originates from soil.

Correction to: Distributions of tritium and 137Cs in coastal seawater and biota off Aomori and Iwate prefectures, Japan

Correction to: Distributions of tritium and 137Cs in coastal seawater and biota off Aomori and Iwate prefectures, Japan

Radioactivity concentration and radiological risk assessment of beach sand along the coastline in the Mediterranean Sea

A radiological baseline survey was conducted using a calculation analysis to assess the 226Ra, 232Th, 40K, and 137Cs distribution in beach sand samples collected from the coastal areas of the Mediterranean Sea. An analysis of the activity concentration of selected radionuclides was conducted. No evidence of recent migration of radiocaesium was found through precipitation, as well as indirect pathways, such as ocean runoff. The activity concentration of 226Ra, 232Th, 40K and 137Cs in beach sands ranged from 12 ± 1 to 37 ± 4 Bq kg− 1 (mean of 26 ± 3 Bq kg− 1); 18 ± 2 to 71 ± 8 Bq kg− 1 (mean of 40 ± 5 Bq kg− 1); 411 ± 10 to 720 ± 16 Bq kg− 1 (mean of 572 ± 12 Bq kg− 1); and 0.8 ± 0.1 to 3.1 ± 0.6 Bq kg− 1 (mean of 1.9 ± 0.3 Bq kg− 1), respectively. The radiological risk assessment showed that in all cases the values were lower than those that endanger life and safe work.

Long-term study (1987-2023) on the distribution of 137Cs in soil following the Chernobyl nuclear accident: a comparison of temporal migration measurements and compartment model predictions.

After the Chernobyl accident, a designated area of ~1000m2 within the University farm of Aristotle University of Thessaloniki in Northern Greece was utilized as a test ground for radioecological measurements. The profile of 137Cs in the soil was monitored from 1987 to 2023, with soil samples collected in 5-cm-thick slices (layers) down to a depth of 30cm. The mean total deposition of 137Cs in the area, backdated to the time of the Chernobyl accident, was determined to be 18.6±1.8kBqm-2 based on four follow-up profile measurements of 137Cs in the soil for the years 2022 and 2023. It is noteworthy that this value is similar the total deposition at the site, which was independently measured to be about 20kBqm-2 during the first year after the Chernobyl accident. The fractional contribution of each soil layer (e.g., 0-5cm, 5-10cm, 10-15cm, etc.) to the total deposition of 137Cs (0-30cm) is presented and analyzed. A compartment model was utilized to forecast the temporal evolution of fractional contributions of the different soil layers to the total deposition of 137Cs (0-30cm). In this model, each soil layer is represented as a separate compartment. The model assumes that the transfer rates between adjacent compartments are equal. The agreement between the measured fractional contributions and the model predictions suggests that the compartment model with equal transfer rates can capture the broad patterns of 137Cs migration within the soil layers over the long period of 1987-2023. However, the use of a second compartment model with increasing transfer rates between consecutive soil layers did not align with the observed outcomes. This indicates that diffusion may not be the primary migration mechanism over the 36-y period covered by our study.