Uptake of radiocesium by mushrooms

After the Chernobyl accident in April 1986 the 134Cs, 137Cs and 40K activity of mushrooms of different genera and their corresponding soils from woods located in the province of Umbria (Italy) was determined. The results indicated: a temporally increasing trend for 137Cs up to a "limit value" depending on local fallout in 1986; different cesium concentrations in various mushroom genera; and uptake of potassium from soil that did not appear to compete with cesium uptake. No reliable correlation can be inferred between the cesium content of the soil and those of mushrooms.     

Radiocaesium activity concentrations in the fruit-bodies of macrofungi in Great Britain and an assessment of dietary intake habits.

Radiocaesium activity concentrations in the fruit-bodies of some species of macrofungi are higher than in many other foodstuffs. The consumption of fruit-bodies contributes significantly to radiocaesium intake of humans in some countries. In the United Kingdom, the collection of wild fungi has generally been considered to be of minor importance and there are few data on consumption rates or radiocaesium activity concentrations in most edible species. Samples of commonly eaten species in Great Britain have been collected to assess radiocaesium contamination levels and geographical variation. Concurrently, surveys of consumption habits were conducted. A total of 425 samples representing 37 different species were collected. Significantly higher radiocaesium activity concentrations occurred in mycorrhizal compared to saprotrophic or parasitic species. The highest 137Cs activity concentration of 30.5 kBq kg-1 dry wt. was determined in a sample of Hydnum repandum collected in Wales. The transfer of radiocaesium from soil to fungal fruit-bodies was highly variable, ranging over three orders of magnitude within individual species. A number of approaches to quantifying radiocaesium transfer from soil to fungal fruit-bodies were used. Although these were in general agreement with previously measured values in other countries, all the approaches gave variable results. Over 200 people responded to the dietary habits questionnaire. The median intake rate was 0.75 kg year-1 (fresh wt.) and 60% of respondents consumed only one species (generally Agaricus campestris). However, intakes of up to 26 kg year-1 were recorded and a total of 82 species were consumed. The intake of 137Cs was determined by the amount of mycorrhizal fungi in the diet rather than the total intake of fungi. Assuming median recorded 137Cs activity concentrations in each fungal species, the estimated annual committed effective dose for over 95% of respondents was < 1 microSv. Hence, currently, the consumption of wild fungi in the UK would not be expected to significantly increase the dose above that attributable to the normal diet of most consumers. However, the results of this study demonstrate that, in the event of any future accidental release of radiocaesium, the potential ingestion dose received from the consumption of wild fungi would need to be considered.     

137Cs in the fungal compartment of Swedish forest soils

The (137)Cs activities in soil profiles and in the mycelia of four ectomycorrhizal fungi were studied in a Swedish forest in an attempt to understand the mechanisms governing the transfer and retention of (137)Cs in forest soil. The biomass of four species of fungi was determined and estimated to be 16 g m(-2) in a peat soil and 47-189 g m(-2) in non-peat soil to the depth of 10 cm. The vertical distribution was rather homogeneous for two species (Tylospora spp. and Piloderma fallax) and very superficial for Hydnellum peckii. Most of the (137)Cs activity in mycelium of non-peat soils was found in the upper 5 cm. Transfer factors were quite high even for those species producing resupinate sporocarps. In the peat soil only approximately 0.3% of the total (137)Cs inventory in soil was found in the fungal mycelium. The corresponding values for non-peat soil were 1.3, 1.8 and 1.9%.     

Migration of fallout radiocaesium in a grassland soil from 1986 to 2001. Part I: activity-depth profiles of (134)Cs and (137)Cs

The temporal changes of the vertical distribution of (134)Cs (deposited by the Chernobyl fallout in 1986) and (137)Cs (deposited by the Chernobyl and the global fallout) in the soil were investigated at an undisturbed Bavarian grassland site in Germany. At ten sampling dates between 1986 and 2001, the activity density of (134)Cs and (137)Cs was determined in various soil layers down to 80 cm depth. In 2001, the small-scale spatial variability of the radiocaesium activity was determined by sampling five plots within 10 m(2) (coefficient of variation about 20% for the upper soil layers). Between 1987 and 1990, substantial changes of the activity-depth profiles were observed. The percentage depth distributions of (134)Cs and (137)Cs were rather similar. The 50%-depth of the accumulated activity increased from 2.4 cm in 1988 to 5.3 cm in 2001 for (134)Cs and from 2.7 to 5.8 cm for (137)Cs. This indicates that at the study site the migration data of Chernobyl-derived (137)Cs can be estimated by those of total (137)Cs. In the second part of this study, the activity-depth profiles will be evaluated by the convection-dispersion model [Schimmack, W, Feria Márquez, F. Migration of fallout radiocaesium in a grassland soil from 1986 to 2001. Part II: Evaluation of the activity-depth profiles by transport models. Sci Total Environ 2006-this issue].     

137Cs loss via soil erosion from a mountainous headwater catchment in central Japan

Eroded sediment and coarse organic material were sampled for a year at the outlet of the study catchment in central Japan to investigate characteristics of 137Cs loss and to quantify erosional 137Cs loss in a forested headwater catchment. Results showed that loss of both eroded sediment and 137Cs varied markedly according to the magnitude of rainfall events. About 90% of the total sediment delivery and the total 137Cs loss was associated with only two storm rainfall events. The significant contribution of high-magnitude-low-frequency storm events to 137Cs loss from the catchment was emphasized. To quantify the contribution of erosional 137Cs loss to 137Cs cycling, the current mean 137Cs inventory of the study catchment was estimated from direct measurements of 137Cs in soil cores collected from 27 points. The input of 137Cs through litterfall to the soil was estimated from monitoring the annual litterfall of the study catchment. The present 137Cs fallout input was estimated from published 137Cs fallout data. Consequently, the loss of 137Cs associated with eroded sediment was estimated to represent 0.013% of the 137Cs inventory of the study catchment, which is comparable to the input through litterfall. The equivalent value for 137Cs runoff with coarse organic material was estimated as 0.0003%. Therefore, the effect of 137Cs loss in association with coarse organic material on estimates of erosion rate obtained by measuring 137Cs inventories in soil core samples was inferred to be negligible in Japanese cypress plantations. Results confirm the applicability of 137Cs measurements to estimate erosion rates in other relatively stable forested areas.     

Application of potassium chloride to a Chernobyl-contaminated lake: modelling the dynamics of radiocaesium in an aquatic ecosystem and decontamination of fish

This study tests a whole-lake experiment to reduce the bioaccumulation of radiocaesium (137Cs) in fish in lakes contaminated by the Chernobyl accident. In many lakes in the Chernobyl contaminated areas, radiocaesium activity concentrations in fish are still significantly higher (up to 100 times in some species) than acceptable limits for human consumption. Estimates of the long-term rate of decline of 137Cs in fish in these regions, in the absence of countermeasures, show that radioactivity in fish in some lakes may remain above acceptable consumption limits for a further 50-100 years from the present date. In February 1998 we applied 15 t of potassium chloride to Lake Svyatoe, Kostiukovichy. The addition of potassium chloride fertilizer to the lake resulted in a decrease in activity concentration of 137Cs to approximately 40% of pre-countermeasure values in a number of different fish species. In contrast to Lake Svyatoe, 137Cs activity concentrations in fish from four control lakes showed no systematic decrease over the study period. Simplified models for transfers of 137Cs in lakes successfully 'blind' predicted the changes in 137Cs in water and fish resulting from this major alteration of the potassium concentration of the lake. The experiment represents the first test of a predictive model for the dynamics of radiocaesium in response to a major perturbation in potassium (its major competitor ion) in a whole lake ecosystem.     

137Cs, 239+240Pu and 240Pu/239Pu atom ratios in the surface waters of the western North Pacific Ocean, eastern Indian Ocean and their adjacent seas

Surface seawater samples were collected along the track of the R/V Hakuho-Maru cruise (KH-96-5) from Tokyo to the Southern Ocean. The (137)Cs activities were determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas, the eastern Indian Ocean, the Bay of Bengal, the Andaman Sea, and the South China Sea. The (137)Cs activities showed a wide variation with values ranging from 1.1 Bq m(-3) in the Antarctic Circumpolar Region of the Southern Ocean to 3 Bq m(-3) in the western North Pacific Ocean and the South China Sea. The latitudinal distributions of (137)Cs activity were not reflective of that of the integrated deposition density of atmospheric global fallout. The removal rates of (137)Cs from the surface waters were roughly estimated from the two data sets of Miyake et al. [Miyake Y, Saruhashi K, Sugimura Y, Kanazawa T, Hirose K. Contents of (137)Cs, plutonium and americium isotopes in the Southern Ocean waters. Pap Meteorol Geophys 1988;39:95-113] and this study to be 0.016 yr(-1) in the Sulu and Indonesian Seas, 0.033 yr(-1) in the Bay of Bengal and Andaman Sea, and 0.029 yr(-1) in the South China Sea. These values were much lower than that in the coastal surface water of the western Northwest Pacific Ocean. This was likely due to less horizontal and vertical mixing of water masses and less scavenging. (239+240)Pu activities and (240)Pu/(239)Pu atom ratios were also determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas and the South China Sea. The (240)Pu/(239)Pu atom ratios ranged from 0.199+/-0.026 to 0.248+/-0.027 on average, and were significantly higher than the global stratospheric fallout ratio of 0.18. The contributions of the North Pacific Proving Grounds close-in fallout Pu were estimated to be 20% for the western North Pacific Ocean, 39% for the Sulu and Indonesian Seas and 42% for the South China Sea by using the two end-member mixing model. The higher (240)Pu/(239)Pu atom ratios could be attributed to close-in fallout Pu delivered from the Enewetak and Bikini Atolls by ocean currents of branches of the North Equatorial Current to the Southeast Asian seas.     

Plutonium and 137Cs in surface water of the South Pacific Ocean

The present plutonium and 137Cs concentrations in South Pacific Ocean surface waters were determined. The water samples were collected in the South Pacific mid-latitude region (32.5 degrees S) during the BEAGLE expedition conducted in 2003-04 by JAMSTEC. 239,240Pu concentrations in surface seawater of the South Pacific were in the range of 0.5 to 4.1 mBq m(-3), whereas 137Cs concentrations ranged from 0.07 to 1.7 Bq m(-3). The observed 239,240Pu and 137Cs concentrations in the South Pacific were almost of the same level as those in the North Pacific subtropical gyre. The surface 239,240Pu in the South Pacific subtropical gyre showed larger spatial variations than 137Cs, as it may be affected by physical and biogeochemical processes. The 239,240Pu/137Cs activity ratios, which reflect biogeochemical processes in seawater, were generally smaller than that observed in global fallout, except for the most eastern station. The 239,240Pu/137Cs ratios in the South Pacific tend to be higher than that in the North Pacific. The relationships between anthropogenic radionuclides and oceanographic parameters such as salinity and nutrients were examined. The 137Cs concentrations in the western South Pacific (the Tasman Sea) and the eastern South Pacific were negatively correlated with the phosphate concentration, whereas there is no correlation between the 137Cs and nutrients concentrations in the South Pacific subtropical gyre. The mutual relationships between anthropogenic radionuclides and oceanographic parameters are important for better understanding of transport processes of anthropogenic radionuclides and their fate in the South Pacific.     

137Cs in the western South Pacific Ocean

The 137Cs activities were determined for seawater samples from the East Caroline, Coral Sea, New Hebrides, South Fiji and Tasman Sea (two stations) Basins of the western South Pacific Ocean by gamma spectrometry using a low background Ge detector. The 137Cs activities ranged from 1.4 to 2.3 Bq m(-3) over the depth interval 0-250 m and decreased exponentially from the subsurface to 1000 m depth. The distribution profiles of 137Cs activity at these six western South Pacific Ocean stations did not differ from each other significantly. There was a remarkable difference for the vertical profiles of 137Cs activity between the East Caroline Basin station in this study and the GEOSECS (Geochemical Ocean Sections Study) station at the same latitude in the Equatorial Pacific Ocean; the 137Cs inventory over the depth interval 100-1000 m increased from 400+/-30 Bq m(-2) to 560+/-30 Bq m(-2) during the period from 1973 to 1992. The total 137Cs inventories in the western South Pacific Ocean ranged from 850+/-70 Bq m(-2) in the Coral Sea Basin to 1270+/-90 Bq m(-2) in the South Fiji Basin. Higher 137Cs inventories were observed at middle latitude stations in the subtropical gyre than at low latitude stations. The 137Cs inventories were 1.9-4.5 times (2.9+/-0.7 on average) and 1.7-4.3 times (3.1+/-0.7 on average) higher than that of the expected deposition density of atmospheric global fallout at the same latitude and that of the estimated 137Cs deposition density in 10 degrees latitude by 10 degrees longitude grid data obtained by Aoyama et al. [Aoyama M, Hirose K, Igarashi Y. Re-construction and updating our understanding on the global weapons tests 137Cs fallout. J Environ Monit 2006;8:431-438], respectively. The possible processes for higher 137Cs inventories in the western South Pacific Ocean than that of the expected deposition density of atmospheric global fallout may be attributable to the inter-hemisphere dispersion of the atmospheric nuclear weapons testing 137Cs from the northern stratosphere to the southern one and its subsequent deposition, and water-bearing transport of 137Cs from the North Pacific Ocean to the western South Pacific.     

Radiocaesium and natural gamma emitters in mushrooms collected in Spain

Mushrooms can accumulate heavy metals in general, including radionuclides found in the nature. However, little attention has been paid to the radioactive content of mushrooms collected in Spain and the dose for the population due to their ingestion. To address this, we analysed the contents of 137Cs, 40K, 226Ra and 7Be present in different species of mushrooms, according to their genus and nutritional mechanism. We observed that mycorrhizal mushrooms accumulate 137Cs more than saprophytes, and vice versa for 7Be. 40K and 226Ra are accumulated to the same degree by the two groups of mushrooms. We estimated the dose due to ingestion of mushrooms in Spain to be 2 microSv/year, and the contribution of 40K and 226Ra to be generally greater than that of 137Cs. The contribution of 137Cs to the dose was calculated by taking into account the results of an experiment carried out under the controlled laboratory conditions, which showed that approximately 98% of 134Cs was associated with the readily digestible fraction of the mushrooms.     

Long-term variations in dissolved trace elements in the Sagami River and its tributaries (upstream area), Japan

We investigated long-term variations in dissolved chemical species in water sampled from the Sagami River and its tributaries, Japan. The samples were taken monthly from May 1993 to April 2000 at 28 sampling sites in the Sagami River system. In this paper, we concentrate on 17 sites in the upper catchment. Twenty-four major to trace elements (Li, Mg, Al, Ca, V, Mn, Fe, Co, Ni, Cu, Zn, As, Rb, Sr, Mo, Ag, Cd, Sb, Cs, Ba, W, Tl, Pb, U) were determined by using conventional Q-pole ICP-MS with direct nebulizalion. Water flux was measured from 1995. The data for most species were subjected to fast Fourier transformation (FFT) to extract dominant periodicities, their magnitudes, and their phases. Clear seasonal variations were observed for Al, V, As, Rb and Cs at some sampling points, especially in the tributaries. The seasonal variations may be due to either anthropogenic causes, such as irrigation or wastewater discharge, or natural causes, such as water temperature, pH, redox condition, water flux, or activity of microorganisms. We found no correlation with pH. Water temperature may not be a main controlling factor, although the seasonal variability would be correlated with it. Hydrologic factors may have only minor effects. We suggest that most of the seasonal variation might be correlated with the irrigation of rice paddies. It was difficult to identify all the causes of the seasonal variability. To investigate interannual trends, we used centered 12-month moving averages to eliminate seasonal variations. The water quality of the uppermost streams was generally constant, being controlled by springs on Mt. Fuji. However, in 1993 and 1998, V, As, Rb, Cs and U were depleted briefly, possibly by dilution by overflow from Lakes Kawaguchi and Yamanaka. Hydrologic factors may be more important for interannual variability than seasonal variability. Some heavy trace elements (Zn, Ni, Cd and Sb) showed very irregular variations with high concentration peaks. These elements were discharged from either factories or abandoned mine tailings.     

Radiocaesium (137Cs) in marine mammals from Svalbard, the Barents Sea and the North Greenland Sea

Specific activities of the anthropogenic radionuclide, 137Cs, were determined in marine mammals from Svalbard and the Barents and North Greenland Seas. Muscle samples were collected from 12 polar bears, 15 ringed seals, 10 hooded seals, 7 bearded seals, 14 harp seals, one walrus, one white whale and one blue whale in the period 2000-2003. The mean concentrations (+/-SD) of 137Cs were: 0.72+/-0.62 Bq/kg wet weight (w.w.) for polar bears; 0.49+/-0.07 Bq/kg w.w. for ringed seals; 0.25+/-0.10 Bq/kg w.w. for hooded seals; 0.22+/-0.11 Bq/kg w.w. for bearded seals; 0.36+/-0.13 Bq/kg w.w. for harp seals; 0.67 Bq/kg w.w. for the white whale sample; 0.24 Bq/kg w.w. for the blue whale; and below detection limit for the walrus. Significant differences in 137Cs specific activities between some of the species were found. Ringed seals had higher specific activities than the other seal species in the study. Bearded seals and hooded seals had similar values, which were both significantly lower than the harp seal values. The results in the present study are consistent with previous reported results, indicating low specific activities of 137Cs in Arctic marine mammals in the Barents Sea and Greenland Sea region during the last 20 years. The species specific differences found may be explained by varying diet or movement and distribution patterns between species. No age related patterns were found in specific activities for the two species (polar bears and hooded seals) for which sufficient data was available. Concentration factors (CF) of 137Cs from seawater were determined for polar bears, ringed, bearded, harp and hooded seals. Mean CF values ranged from 79+/-32 (SD) for bearded seals sampled in 2002 to 244+/-36 (SD) for ringed seals sampled in 2003 these CF values are higher than those reported for fish and benthic organisms in the literature, suggesting bioaccumulation of 137Cs in the marine ecosystem.     

Specific activity and activity ratios of radionuclides in soil collected about 20 km from the Fukushima Daiichi Nuclear Power Plant: Radionuclide release to the south and southwest

Soil samples at different depths (0-2, 5-7 and 10-12 cm) were collected from J Village, about 20 km south of Fukushima Daiichi Nuclear Power Plant (FNPP) to determine their radionuclide specific activities and activity ratios. The concentrations and activity ratios of ¹³¹I, ^{134, 136, 137}Cs and ^129mTe were obtained, but only trace amounts of ⁹⁵Nb, ^110mAg and ¹⁴⁰La were detected which were too low to provide accurate concentrations. Radionuclides such as ⁹⁵Zr, ^{103, 106}Ru and ¹⁴⁰Ba that were found in Chernobyl fallout, were not found in these soil samples. This suggests that noble gasses and volatile radionuclides predominated in the releases from FNPP to the terrestrial environment. The average activity ratios of ¹³¹I/¹³⁷Cs, ¹³⁴Cs/¹³⁷Cs, ¹³⁶Cs/¹³⁷Cs and ^129mTe/¹³⁷Cs were 55, 0.90, 0.22 and 4.0 (corrected to March 11, 2011) in the 0-2 cm soil samples of April 20 and 28, 2011.     

137Cs availability for soil to understory transfer in different types of forest ecosystems

A quantitative analysis of 137Cs bioavailability in forest soils in the long term after the Chernobyl NPP accident based on a 3-year (1996-1998) investigation is presented. Five forest sites with different trees, composition and properties of soil were studied to identify factors determining radiocaesium transfer to different understory species. The following parameters were investigated: 137Cs activity concentrations and its speciation in various horizons of forest soil, accumulation of this radionuclide by different species of understory vegetation and distribution of root biomass in the soil profile. It has been shown that one decade after the deposition maximum 137Cs activity in soil of the experimental sites considered is located in different soil layers dependent on moisture regime, characteristics of litter and soil properties. A linear dependence between aggregated transfer factors for different species and groups of species of understory vegetation and exchangeable and available fractions of radiocaesium in soil was found. The vertical distribution of 137Cs activity, percentage of exchangeable radiocaesium in each horizon of litter and soil, as well as distribution of root systems (mycelia) over the soil profile are key factors governing variations in the availability of 137Cs for transfer to all forest understory components.     

137Cs distribution and geochemistry of Lena River (Siberia) drainage basin lake sediments

The Lena River is the second largest river that discharges into the Arctic Ocean. It is therefore important to determine not only the direct impact its discharge has on the 137Cs concentration of the Arctic, but also the potential its drainage basin has as a 137Cs source. 137Cs surface sediment concentrations and inventory values, which range from 4.97 to 338 Bq kg(-1) and 357 to 1732 Bq m(-2), respectively, were determined for the Lena River drainage basin lake samples, via gamma analysis. The average geochemical and mineralogical composition of a subset of samples was also determined using neutron activation analysis, X-ray diffraction and X-ray fluorescence spectrometry techniques. Results of these geochemical analyses allowed for the identification of key geochemical factors that influence the distribution of 137Cs in the Lena River drainage basin. 137Cs profiles indicate that Lena River drainage basin lacustrine sediments serve as a record of 137Cs fallout. Based on the downcore 137Cs, %illite, %smectite, %Al and %Mn distribution patterns, it was concluded that a small fraction of non-selectively bound 137Cs was remobilized at depth in some cores. Inconsistencies between the actual 137Cs fallout record and the 137Cs profiles determined for the lake sediments were attributed to 137Cs remobilization in subsurface sediments. In addition to establishing the agreement between the global atmospheric fallout record and the downcore 137Cs distribution patterns determined for these sediments, results indicate that 137Cs deposited during periods of maximum atmospheric release was buried and is not susceptible to surface erosion processes. However, mean 137Cs concentrations of the lacustrine surface sediments (125 Bq kg(-1)) are still significantly higher than those of the nearby Lena River estuary (11.22 Bq kg(-1)) and Laptev Sea (6.00 Bq kg(-1)). Our study suggests that the Lena River drainage basin has the potential to serve as a source of 137Cs to the adjacent Arctic Ocean.     

Trace element analysis in the serum and hair of Antarctic leopard seal, Hydrurga leptonyx, and Weddell seal, Leptonychotes weddellii

Leopard seal, Hydrurga leptonyx, and Weddell seal, Leptonychotes weddellii, occupy an upper trophic level within the Antarctic ecosystem and are useful indicator species in the Southern Ocean of trace element concentrations. Reference values for the concentration of 19 trace elements were determined in the serum and hair of leopard and Weddell seals sampled in Eastern Antarctica. These reference values can be used as 'baseline' levels for monitoring trace element concentrations in these species. Greater trace element concentrations were determined in hair compared to serum, indicating different time scales of trace element accumulation in these samples. For the majority of trace elements, except for Se in the leopard seal samples and Cr in the Weddell seal samples, significant regression relationships for trace element concentrations in hair and serum were not elucidated. Significant differences were determined in the concentrations of seven out of 15 elements with hair type, moult and new, in the leopard seal; concentrations in moult hair were determined to be greater than in new hair for all elements except Zn. Hair analysis was determined to be useful for monitoring exposure to trace elements and when collected off the ice from moulting seals, hair can be employed as a non-invasive sample for trace element analysis in leopard and Weddell seals.     

Transfer of 137Cs and stable Cs from soil to potato in agricultural fields.

The concentrations of 137Cs, stable Cs and K were measured in soils and potatoes collected from 26 agricultural fields in Aomori, Japan and soil-to-potato transfer factors of 137Cs and stable Cs were determined. The concentrations of 137Cs derived from fallout deposition and stable Cs in soils were 1-37 Bq kg-1 and 1-11 mg kg-1, respectively. The isotopes, 137Cs and stable Cs, were homogeneously mixed in the rooting zone in the upper 20 cm of soil in agricultural fields. The concentrations of 137Cs and stable Cs in potatoes were 50-2000 mBq kg-1 dry wt. and 0.004-0.13 mg kg-1 dry wt., respectively. The soil-to-potato transfer factor of 137Cs was in the range of 0.0037-0.16, which was higher than that of stable Cs of 0.00052-0.080. The transfer factors of 137Cs and stable Cs were correlated and the geometric mean of 137Cs was 0.030, which was four times higher than that of stable Cs at 0.0075. This implied that artificially added 137Cs is more mobile and more easily absorbed by plants than stable Cs in the soil. The concentration of K in potatoes showed a relatively constant value, independent of that in the soil. The transfer factors of both 137Cs and stable Cs decreased with increasing K concentration in the soil, which was mainly supplied as fertilizers to the fields. This suggests that the transfer of both 137Cs and stable Cs from soil to potato was affected by the presence of K in the soil. However, the transfer factors of 137Cs and stable Cs were independent of the amount of organic materials in soils.     

Distribution of radiocaesium in an Austrian forest stand

Within an Austrian spruce stand, vertical distribution of radiocaesium in soil as well as 137Cs concentration in different forest ecosystem compartments including spruce and surface water were investigated 10 years after the Chernobyl accident. The total 137Cs inventory in the forest was estimated to be 46 kBq m-2 (ref. date: 86-05-01). From the collected data annual input rates via litterfall of 0.48% per year and output rates through waterflows of only 0.02% per year were derived. The results identify the high importance of forest soils as a sink for radiocaesium. The estimated ecological residence half-times turned out to be highest in the organic soil horizons (1-3 years per cm), whereas in mineral horizons the values decrease significantly. As a consequence, soil inventory represents more than 95% of the total, whereas only approximately 3.3% of the 137Cs inventory is stored in the living biomass of spruce trees and a further 0.5% in the phytomass of understorey vegetation.     

Assessment of Committed Effective Dose due to consumption of Red Sea coral reef fishes collected from the local market (Sudan)

An assessment of Committed Effective Dose (CED) due to consumption of Red Sea fish containing (210)Po and (137)Cs was performed for 23 different marine fish samples collected from the local market at Port Sudan. The fish were classified according to their feeding habits into three categories: carnivores, herbivores, and omnivores. Measured activity concentrations of (210)Po were found in the ranges 0.25-6.42 (carnivores), 0.7-5 (omnivores) and 1.5-3.8 (herbivores) Bq/kg fresh weight. In the same study, activity concentrations of Cs-137 were determined to be in the ranges 0.1-0.46 (carnivores), 0.09-0.35 (omnivores) and 0.09-0.32 (herbivores) Bq/kg fresh weight, which were several times lower than those of (210)Po. Appropriate conversion factors were used to derive the CED, which was found to be 0.012, 0.01 and 0.01 (microSv/yr) in carnivores, omnivores and herbivores, respectively, for (137)Cs. This contributes about 0.4% of the total dose exclusively by ingestion of fish. For (210)Po, it was found to be 3.47, 4.81 and 4.14 (microSv/yr) in carnivores, omnivores and herbivores, respectively, which represents 99.6% of the total dose (exclusively by ingestion of fish). The results of CED calculations suggest that the dose received by the Sudanese population from the consumption of marine fish is rather small and that the contribution of (137)Cs is negligible compared to (210)Po.