Long-term changes in 90Sr pools of Scots pine biomass in the Chornobyl Red Forest.

The trenches of the waste burial site in the Chornobyl Red Forest represent a big reservoir of radionuclides for the artificial plantation of Scots pine established in that area, but the long term dynamics of tree biomass contamination, especially with 90Sr, remains unclear. The present study was conducted between 2005 and 2018 on two groups of trees of the same age. The IN group is represented by trees growing on the trench containing highly radioactive contaminated fertile soil and organic matter, while the OUT group is located outside the trench. Within a little more than one decade, the total aboveground biomass doubled in the trees of the group OUT and increased more than four times in the group IN. In the group OUT, the concentrations of 90Sr have decreased in all biomass compartments compared to 2005, while in the group IN, the concentrations demonstrated a trend to increase. Regression analysis shows that both decrease in the compartment concentrations in the group OUT (slope coefficient 0.55) and increase in the group IN (1.58) were significant. As a result of the changes in the biomass inventories and 90Sr concentrations, in absence of changes in plantation density, the contamination of total aboveground biomass by 90Sr in the group OUT would have increased slightly in 2018 (from approximately 18 GBq ha-1 to 23 GBq ha-1) compared to 2005, while in the group IN it would have increased almost 6-fold, reaching approximately 560 GBq ha-1, or about (19 ± 9) % of the total 90Sr inventory in the trench area. Trenches of the Red Forest were shown to act as long-lasting hot spots of 90Sr bioavailability for forest trees.

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.

How dynamic transfer models can complement an equilibrium-based approach: Case studies of radiocesium transfer to forest trees following accidental atmospheric release.

Accidental release of radionuclides caused by nuclear accidents like those in Fukushima and Chernobyl can result in pulses of radioactivity entering the forest environment. Due to intense recycling in the forest, equilibrium between radioactivity concentrations in trees and in soil may not be reached during the period of short-term radionuclide transport following the accident. Another question arises as to whether the equilibrium hypothesis using empirical concentration ratios (CRs) can be applied to the long-term period. Using two atmospheric 137Cs fallout scenarios in the Fukushima and Chernobyl sites, this study investigated whether the CR approach could provide conservative predictions of 137Cs levels in trees following 137Cs fallout events by comparing predictions from the CR approach using data gathered for trees by the IAEA to those from dynamic transfer models and actual measured data. The inter-comparisons also aimed to investigate whether the CR approach could account for the variability of 137Cs levels across different tree organs. The results showed that caution may be necessary when using the CR approach, which relies on the IAEA dataset, to estimate 137Cs accumulation in forest trees in the short - and long term following atmospheric 137Cs fallout events. A calculation by TRIPS 2.0 demonstrated the importance of considering the distribution within tree organs for in-depth analysis of radiological impact of forest trees. Our findings suggest that it may be preferable to use CR values based on site-specific data rather than generic data collected from various sites. This is particularly relevant when studying the sites where the bioavailability of 137Cs for trees and thus possible exposures are higher. This study also showed that dynamic modeling approaches could offer an alternative means of estimating CR values of the entire tree or specific tree organs in situations where empirically derived values are not available.

Recycling and persistence of iodine 127 and 129 in forested environments: A modelling approach.

Differences in the source and behaviour of 129I compared to 127I isotopes have been described for a variety of surface environments, but little is known about the cycling rates of each isotope in terrestrial ecosystems. We developed a compartment model of the iodine cycle in a forest ecosystem, with a labile and non-labile pool to simplify the complex fate of iodine in the forest floor and soil. Simulations were performed using atmospheric 127I and 129I inputs for sites differing in climate, vegetation, and soil. In general, considering dry deposition in addition to wet deposition improved model simulations. Model results support the view that soil is the sink for atmospheric iodine deposited in forest ecosystems, while tree vegetation has little influence on long-term iodine budgets. Modelling also showed that iodine cycling reaches equilibrium after a period of about 5000 years, mainly due to a gradual incorporation of iodine into the bulk stabilised soil organic matter. At steady state, this pool of non-labile iodine in soil can retain about 20% of total deposition with a mean residence time of 900 years, while the labile iodine pool is renewed after 90 years. The proportions of modern anthropogenic 129I in each modelled pool reflect those of stable 127I at least several decades after input to the forest; this result explains why isotopic disequilibrium is common in field data analysis. Volatilisation plays a central role in regulating iodine storage in soil and, therefore, its residence time, while drainage is a minor export pathway, except at some calcareous sites. Dynamic modelling has been particularly helpful for gaining insight into the long-term response of iodine partitioning to continuous, single or even varying deposition. Our modelling study suggested that better estimates of dry deposition of atmospheric iodine, weathering of parent rock, and volatilisation of the deposited iodine from soil and vegetation will be required for reliable predictions of iodine cycling in specific forests, because these processes remain insufficiently explored.

Chlorination of soil organic matter: The role of humus type and land use.

The levels of natural organic chlorine (Clorg) typically exceed levels of chloride in most soils and is therefore clearly of high importance for continental chlorine cycling. The high spatial variability raises questions on soil organic matter (SOM) chlorination rates among topsoils with different types of organic matter. We measured Clorg formation rates along depth profiles in six French temperate soils with similar Cl deposition using 36Cl tracer experiments. Three forest sites with different humus types and soils from grassland and arable land were studied. The highest specific chlorination rates (fraction of chlorine pool transformed to Clorg per time unit) among the forest soils were found in the humus layers. Comparing the forest sites, specific chlorination was highest in mull-type humus, characterized by high microbial activity and fast degradation of the organic matter. Considering non-humus soil layers, grassland and forest soils had similar specific chlorination rates in the uppermost layer (0-10 cm below humus layer). Below this depth the specific chlorination rate decreased slightly in forests, and drastically in the grassland soil. The agricultural soil exhibited the lowest specific chlorination rates, similar along the depth profile. Across all sites, specific chlorination rates were correlated with soil moisture and in combination with the patterns on organic matter types, the results suggest an extensive Cl cycling where humus types and soil moisture provided best conditions for microbial activity. Clorg accumulation and theoretical residence times were not clearly linked to chlorination rates. This indicates intensive Cl cycling between organic and inorganic forms in forest humus layers, regulated by humic matter reactivity and soil moisture, while long-term Clorg accumulation seems more linked with overall deep soil organic carbon stabilization. Thus, humus types and factors affecting soil carbon storage, including vegetation land use, could be used as indicators of potential Clorg formation and accumulation in soils.

Influence of tree species on selenium and iodine partitioning in an experimental forest ecosystem.

Storage of selenium and iodine can greatly vary between forest ecosystems, but the influence of tree species on partitioning and recycling of those elements remains elusive. In this study, contents of Se and I were measured in tree compartments, litterfall, humus, and soil horizons in monospecific stands of Douglas fir, pine, spruce, beech, and oak under identical climatic and edaphic conditions. The cycle of each element was characterized in terms of stocks and fluxes. Lowest concentrations were in wood (Se: 8-13 µg kg-1; I: <16.5 µg kg-1). Senescing organs had higher Se and I content, than the living parts of trees due to direct exposure to atmospheric deposition, with some variation between coniferous and deciduous trees. For all stands, low amounts of Se and I were involved in biological cycle as reflected by low root uptake. In humus, the enrichment of elements greatly increased with the stage of organic matter (OM) degradation with average factors of 10 and 20 for Se and I. OM degradation and element persistence in humus was influenced by tree species. Deciduous trees, with low biomass, and fast degradation of OM stored less Se and I in humus compared to fir and spruce with high humus biomass. Interestingly, tree species did not affect soil reserves of Se and I. Concentration ranges were 331-690 µg Se kg-1 and 4.3-14.5 mg I kg-1. However, the divergent vertical profiles of the elements in the soil column indicated greater mobility of I. Selenium concentrations regularly decreased with depth in correlation with OM and Fe oxides content. For iodine, the maximum iodine concentration at a soil depth of 15 to 35 cm was caused by a parallel precipitation/sorption behavior of aluminium and organic iodine dissolved in the topsoil.

Dynamics of radiocaesium within forests in Fukushima-results and analysis of a model inter-comparison.

Forests cover approximately 70% of the area contaminated by the Fukushima Daiichi Nuclear Power Plant accident in 2011. Following this severe contamination event, radiocaesium (137Cs) is anticipated to circulate within these forest ecosystems for several decades. Since the accident, a number of models have been constructed to evaluate the past and future dynamics of 137Cs in these forests. To explore the performance and uncertainties of these models we conducted a model inter-comparison exercise using Fukushima data. The main scenario addressed an evergreen needleleaf forest (cedar/cypress), which is the most common and commercially important forest type in Japan. We also tested the models with two forest management scenarios (decontamination by removal of soil surface litter and forest regeneration) and, furthermore, a deciduous broadleaf forest (konara oak) scenario as a preliminary modelling study of this type of forest. After appropriate calibration, the models reproduced the observed data reliably and the ranges of calculated trajectories were narrow in the early phase after the fallout. Successful model performances in the early phase were probably attributable to the availability of comprehensive data characterizing radiocaesium partitioning in the early phase. However, the envelope of the calculated model end points enlarged in long-term simulations over 50 years after the fallout. It is essential to continue repetitive verification/validation processes using decadal data for various forest types to improve the models and to update the forecasting capacity of the models.

Selenium distribution in French forests: Influence of environmental conditions.

Selenium is a trace element and an essential nutrient. Its long-lived radioisotope, selenium 79 is of potential radio-ecological concern in surface environment of deep geological repository for high-level radioactive waste. In this study, the influence of environmental, climatic and geochemical conditions on stable Se (as a surrogate of 79Se) accumulation was statistically assessed (PCA analysis, Kruskall-Wallis and Spearman tests) based on the analysis of its concentration in litterfall, humus, and soil samples collected at 51 forest sites located in France. Selenium concentrations were in the ranges: 22-369, 57-1608 and 25-1222 µg kg-1 respectively in litterfall, humus, and soil. The proximity of the ocean and oceanic climate promoted Se enrichment of litterfall, likely due to a significant reaction of wet deposits with forest canopy. Se content was enhanced by humification (up to 6 times) suggesting that Se concentrations in humus were affected by atmospheric inputs. Selenium stock in humus decreased in the order of decreasing humus biomass and increasing turnover of organic matter: mor > moder > mull. Positive correlations between Se content and geochemical parameters such as organic carbon content, total Al and total Fe confirmed the important role of organic matter (OM) and mineral Fe/Al oxides in Se retention in soils.

Atmospheric iodine, selenium and caesium depositions in France: II. Influence of forest canopies.

Estimation of the canopy influence on atmospheric inputs of iodine (I), selenium (Se) and caesium (Cs) in terrestrial ecosystems is an essential condition for appropriate biogeochemical models. However, the processes involved in rain composition modifications after its passage through forest canopy have been barely studied for these elements. We monitored I, Se and Cs concentrations in both rainfall and throughfall of fourteen French forested sites throughout one year, and estimated dry deposition and canopy exchange fluxes for these elements, as well as speciation of I and Se. Comparison of rainfall and throughfall elemental composition highlighted an important impact of forest canopy on both (i) concentrations and fluxes of I, Se and Cs, and (ii) I and Se species. For the three elements, most of their throughfall concentrations were higher than corresponding rainfall. The increase of throughfall elemental fluxes was mostly due to dry deposition for I and Se although the canopy exchange model revealed some sorption within the canopy in most cases; for Cs, foliage leaching was most influencing. Regarding speciation, iodine species in rainfall were highly modified by forest canopy with an important increase of unidentified I proportion in throughfall (on average 49 and 82% in rainfall and throughfall, respectively), possibly due to washoff of dry deposition and/or to transformation into organic forms. Similarly, while rainfall was composed of 26-54% of inorganic Se, inorganic species were undetectable in throughfall. This dataset represents key information to improve modelling of I, Se and Cs cycling within forest ecosystems.

Atmospheric iodine, selenium and caesium depositions in France: I. Spatial and seasonal variations.

The spatial distribution and seasonal variations of atmospheric iodine (I), selenium (Se) and caesium (Cs) depositions remain unclear and this precludes adequate inputs for biogeochemical models. We quantified total concentrations and fluxes of these elements in rainfalls from 27 monitoring sites in France with contrasted climatic conditions; monthly measurements were taken over one year (starting in 2016/09). Since speciation of I and Se can impact their behaviour in the environment, analysis of their inorganic compounds was also conducted. Our results showed that annual I concentrations in rainfall were much higher than those of Se and Cs (annual means = 1.56, 0.044 and 0.005 µg L-1, respectively). The annual iodine concentrations were highly positively correlated with those of marine elements (i.e. Na, Cl and Mg), involving higher I concentrations under oceanic climate than for transition, continental and mountainous ones. Furthermore, common patterns were found between Se concentrations and both marine and terrestrial components consistent with the various sources of Se in atmosphere. The association of Cs with two anthropogenic components (i.e. NH4+ and NO3-) used in agriculture supports the hypothesis of its terrestrial origin (i.e. from atmospheric dusts) in rainfall. We found higher rainfall concentrations of I during the warmest months for all climates. However, no specific seasonal trend occurred for Se and Cs. On annual average, rainfall contained mostly unidentified selenium compounds (inorganic Se proportions = 25-54%) and equal proportions of inorganic and unidentified I compounds. Concentrations of iodate were higher under oceanic climate consistent with an iodine marine-origin.

A dataset of 137Cs activity concentration and inventory in forests contaminated by the Fukushima accident.

The majority of the area contaminated by the Fukushima Daiichi Nuclear Power Plant accident is covered with forests. We developed a dataset for radiocaesium (137Cs) in trees, soil, and mushrooms measured at numerous forest sites. The 137Cs activity concentration and inventory data reported in scientific journal papers written in English and Japanese, governmental reports, and governmental monitoring data on the web were collated. The ancillary information describing the forest stands were also collated, and further environmental information (e.g. climate) was derived from the other databases using longitude and latitude coordinates of the sampling locations. The database contains 8593, 4105, and 3189 entries of activity concentration data for trees, soil, and mushrooms, and 471 and 3521 entries of inventory data for trees and soil, respectively, which were collected from 2011 to 2017, and covers the entire Fukushima prefecture. The data can be used to document and understand the spatio-temporal dynamics of radiocaesium in the affected region and to aid the development and validation of models of radiocaesium dynamics in contaminated forests.

Vertical distributions of radiocesium in Japanese forest soils following the Fukushima Daiichi Nuclear Power Plant accident: A meta-analysis.

This study investigated the temporal change in vertical distributions of radiocesium inventories in Japanese forest soils during the early phase (from 2011 to 2017) following the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident, using three simple parameters. We calculated the fraction in the organic layer (Fl/t), the migration center (Xc) and the relaxation depth (α) using 99 soil inventory data sets. Fl/t decreased significantly from 2011 to 2017 (logistic analysis, p < 0.001). In addition, Fl/t in the FDNPP zone rapidly decreased compared to that in the Chernobyl Nuclear Power Plant (ChNPP) zone from the first year to the second year. Different migration rates from organic to mineral soil layers between previous studies in the ChNPP and this study have several possible causes such as organic litter features, climate and physico-chemical forms of initial deposition. In mineral soil layers in the FDNPP zone, only Xc increased significantly with time according to generalized mixed model analysis (p < 0.01). However, Xc and α in the ChNPP zone decreased from two to five years after the accident in 1986, which shows a high 137Cs retention in the organic layer even in the fifth year after the accident. The vertical migration of 137Cs in the mineral soil layer in the FDNPP zone appears to be due to low input of 137Cs from organic to surface mineral soil layer after the second year. These results indicate that 137Cs retention capacity of the organic layer can affect the apparent vertical migration of 137Cs in the underlying mineral soil layer.

Soil organic matter affects arsenic and antimony sorption in anaerobic soils.

Soil organic matter (SOM) affects arsenic (As) and antimony (Sb) mobility in soils under waterlogged conditions by acting as an electron donor, by catalyzing redox-cycling through electron shuttling and by acting as a competing ligand. This study was set up to disentangle these different effects of SOM towards As and Sb sorption in anaerobic soils. Nine samples were taken at different depths in an agricultural soil profile to collect samples with a natural SOM gradient (<1-40 g soil organic carbon kg-1). The samples were incubated either or not under waterlogged conditions in an anaerobic chamber for 63-70 days, and glucose (5 g C kg-1) was either or not added to the anaerobic incubated samples as an electron donor that neither acts as an electron shuttle nor as a competing ligand. The solid-liquid distribution coefficients (KD) of As and Sb were measured at trace levels. The KD values of As decreased ∼2 orders of magnitude upon waterlogging the SOM rich topsoil, while no additional changes were observed when glucose was added. In contrast, smaller changes in the As KD values were found in the low SOM containing subsoil samples, unless glucose was added that mobilised As. The Sb KD values increased upon reducing conditions up to factor 20, but again only in the high SOM topsoil samples. Surprisingly, the Sb immobilisation during waterlogging only occurred in Sb amended soils whereas the geogenic Sb was mobilised upon reducing conditions, although total dissolved Sb concentrations remained low (<10 nM). The change in As and Sb sorption upon waterlogging was similar in the SOM rich topsoil as in the low SOM subsoil amended with glucose. This suggests that the SOM dependent changes in As and Sb mobility in response to soil waterlogging are primarily determined by the role of SOM as electron donor.

Assessing the recycling of chlorine and its long-lived 36Cl isotope in terrestrial ecosystems through dynamic modeling.

It is unclear to what extent chlorine (Cl) and its long-lived isotope 36Cl are recycled in different terrestrial environments in response to time-variable inputs. A new version of a dynamic compartment model was developed to examine the transformation and transfer processes influencing the partitioning and persistence of both Cl and 36Cl in forest ecosystems. The model's performance was evaluated by comparing simulations and field observations of scenarios of stable Cl atmospheric deposition and of global 36Cl fallout. The model reproduced Cl storage in soil reasonably well, despite wide heterogeneity in environmental conditions and atmospheric deposits. Sensitivity analysis confirmed that the natural production of organochlorine in soil plays a major role in Cl build-up and affects long-term Cl dynamics. The timeframe required for the soil organochlorine pool to reach equilibrium in a steady-state system was several thousands of years. Interestingly, root uptake flux, a predominant pathway of the inorganic cycle, was found to affect both inorganic and organic pools in soil, highlighting the importance of plant-soil interactions in Cl dynamics. Model outputs agreed well with local 36Cl measurements, and demonstrated that 90% of the 36Cl found in soil may have come from bomb-test fallout. The pattern of estimated 36Cl/Cl ratios showed that soil 36Cl was not in equilibrium with 36Cl levels in rain input in the post-bomb period. Complete recovery of a natural isotopic ratio in drainage water will need a time close to the residence time of organic 36Cl in soil: i.e., 800 years. A simple dynamic model concept was found to be suitable to illustrate the plant-soil interactions combining both the inorganic and organic Cl cycles acting over different time scales.

Iodine budget in forest soils: Influence of environmental conditions and soil physicochemical properties.

Due to its longevity, radioisotope 129I is a health concern following potential releases in the environment which raises questions about residence and exposure times relevant for risk assessments. We determined 127I concentrations (as a surrogate for 129I) in a series of French forest soils (i.e. litters, humus and mineral soils) under different vegetation and climate conditions in order to identify the major processes affecting its accumulation and persistence in the soil column. The input fluxes linked to rainfall, throughfall and litterfall were also characterized. Main results obtained showed that: (i) rainfall iodine concentrations probably influenced those of litterfall through absorption by leaves/needles returning to the ground; (ii) throughfall was the major iodine input to soils (mean = 83%), compared to litterfall (mean = 17%); (iii) humus represented a temporary storage of iodine from atmospheric and biomass deposits; (iv) iodine concentrations in soils depended on both the iodine inputs and the soil's ability to retain iodine due to its organic matter, total iron and aluminium concentrations; (v) these soil properties were the main factors influencing the accumulation of iodine in the soil column, resulting in residence times of 419-1756 years; and (vi) the leaching of iodine-containing organic matter dissolved in soil solution may be an important source of labile organic iodine for groundwater and streams.

Iodine distribution and cycling in a beech (Fagus sylvatica) temperate forest.

Radioiodine is of health concerns in case of nuclear events. Possible pathways and rates of flow are essential information for risk assessment. Forest ecosystems could influence the global cycle of long-lived radioiodine isotope (129I) with transfer processes similar to stable isotope (127I). Understanding iodine cycling in forest involves study of the ecosystem as a whole. In this context, we determined the 127I contents and distribution in soil, tree compartments and atmospheric inputs during a three years in situ monitoring of a temperate beech forest stand. The iodine cycle was first characterized in terms of stocks by measuring its concentrations in: tree, litterfall, humus, soil, rainfall, throughfall, stemflow and soil solutions. Main annual fluxes (requirement, uptake and internal transfers) and forest input-output budget were also estimated using conceptual model calculations. Our findings show that: (i) soil is the main I reservoir accounting for about 99.9% of ecosystem total stock; (ii) iodine uptake by tree represents a minor fraction of the available pool in soil (<0.2%); (iii) iodine allocation between tree compartments involves low immobilization in wood and restricted location in the roots; (iv) translocation of excess iodine towards senescing foliage appears as an elimination process for trees, and (v) litterfall is a major pathway in the I biological cycling. In our soil conditions, the input - output budget shows that the ecosystem behaves as a potential source of I for groundwater.

Development and assessment of a simple ecological model (TRIPS) for forests contaminated by radiocesium fallout.

The management of vast forested zones contaminated by radiocesium (rCs) following the Chernobyl and Fukushima fallout is of great social and economic concern in affected areas and requires appropriate dynamic models as predictive or questioning tools. Generally, the existing radio-ecological models need less fragmented data and more ecological realism in their quantitative description of the rCs cycling processes. The model TRIPS ("Transfer of Radionuclide In Perennial vegetation Systems") developed in this study privileged an integrated approach which makes the best use of mass balance studies and available explicit experimental data for Scots pine stands. A main challenge was the differentiation and calibration of foliar absorption as well as root uptake in order to well represent the rCs biocycling. The general dynamics of rCs partitioning was simulated with a relatively good precision against an independent series of observed values. In our scenario the rCs biological cycling enters a steady-state about 15 years after the atmospheric deposits. At that time, the simulations showed an equivalent contribution of foliage and root uptake to the tree contamination. But the root uptake seems not sufficient to compensate the activity decline in the tree. The initial foliar uptake and subsequent internal transfers were confirmed to have a great possible impact on the phasing of tree contamination. An extra finding concerns the roots system acting as a buffer in the early period. The TRIPS model is particularly useful in cases where site-specific integrated datasets are available, but it could also be used with adequate caution to generic sites. This development paves the way for simplification or integration of new modules, as well as for a larger number of other applications for the Chernobyl or Fukushima forests once the appropriate data become available. According to the sensitivity analysis that involves in particular reliable estimates of net foliar uptake as well as root uptake not disconnected from rCs exchange reactions in soil.

Radiocaesium partitioning in Japanese cedar forests following the "early" phase of Fukushima fallout redistribution.

Our study focused on radiocaesium (137Cs) partitioning in forests, three vegetation periods after the Fukushima Daiichi nuclear power plant accident. 137Cs distribution in forest components (organic and mineral soil layers as well as tree compartments: stem, bark, needles, branches and roots) was measured for two Japanese cedar stand ages (17 and 33 years old). The results showed that around 85% of the initial deposit was found in the forest floor and topsoil. For the youngest stand almost 70% of the deposit is present in the forest floor, whereas for the oldest stand 50% is present in the 0-3 cm mineral soil layer. For trees, old and perennial organs (including dead and living needles and branches, litter fall and outer bark) directly exposed to the fallout remained the most contaminated. The crown concentrated 61-69% of the total tree contamination. Surprisingly the dead organs concentrated 25 ± 9% (young cedars) to 36 ± 20% (mature cedar) of the trees' residual activity, highlighting the importance of that specific compartment in the early post-accident phase for Japanese cedar forests. Although the stem (including bark) represents the highest biomass pool, it only concentrates 3.3% and 4.6% of the initial 137Cs deposit for mature and young cedars, respectively.