Plutonium,241Am,90sr,and137cs concentrations in some antarctic matrices

A radioecological survey in Antarctica shows that the^239+240Pu,²³⁸Pu,²⁴¹Am,⁹⁰Sr, and¹³⁷Cs activities were detectable in nearly all the samples. The activity level of^239+240Pu,²⁴¹Am, and¹³⁷Cs in antarctic sediments was about 5–20 times lower than in the northern Adriatic Sea sediments, but the²³⁸Pu activities were relatively high. It was interesting to note that the⁹⁰Sr concentrations in all the sediments tended to be low, which could be the result of the easier exchangeable behavior of⁹⁰Sr in water. High concentrations were detected in mosses and lichens and their activity levels were comparable to those in central Italy. The radionuclide ratio analyses show that the major part of^239+240Pu,²⁴¹Am,⁹⁰Sr, and¹³⁷Cs was a result of nuclear weapon tests. The higher²⁴¹Am/^239+240Pu ratio was observed and it could perhaps be the result of fallout of nuclear weapon tests prior to 1962. The²³⁸Pu/^239+240Pu ratio in the antarctic matrices was about seven times higher than in the Northern hemisphere and it could be inferred that the major part of²³⁸Pu was originating from the SNAP-9A satellite accident.     

Solubility of airborne radioactive fuel particles from the Chernobyl reactor and implication to dose

Airborne particles of nuclear fuel from the Chernobyl reactor that had been collected on air filters and stored, were characterised using in vitro dissolution tests to assess effective doses after their inhalation. As solvent, the Gamble biological fluid was used to simulate lung fluid. The solubility of the measured radionuclides decreased in the order ¹³⁷Cs>⁹⁰Sr>>²⁴¹Am^239+240Pu in the simulated lung fluid. The dissolution rate constant of e.g. ^239+249Pu ranged from 0.72 to 5.4×10^–6 g·cm^–2 d^–1 and decreased (for all nuclides) with increasing particle size as predicted from theoretical considerations. Considering the inhalation dose, decreasing dose with size and increasing doses with lower solubility may partly counterbalance each other for ¹³⁷Cs and ⁹⁰Sr. On the other hand, for ²³⁹Pu and ²⁴¹Am larger particles and associated lower solubility both change the resulting dose in the same direction towards lower values. The comparison of the experimentally determined dose coefficients with ICRP values indicates that nuclear fuel particles closely resemble type M material characteristics for ¹³⁷Cs and ⁹⁰Sr and type S material characteristics for ²³⁹Pu and ²⁴¹Am.     

Organic forms of artificial radionuclide compounds in soil solutions from natural biogeocenosis

The date on the distribution of the main radiologicaly important polutants of biosphera (90Sr, 137Cs, 239 + 240Pu, 238Pu, 241Am) over the molecular mass fractions of organic matter in the soil solutions of natural environments are presented. Molecular mass constitution and radionuclide content in the fractions are dependent on radionuclide nature and type of soil and change along the soil profile. The major portion of 238Pu, 239 + 240Pu and 241Am (72-98%) was bound with organic matter in the soil solutions. In the case of organic horizons, these radionuclides were selectively connected with the fractions of high molecular masses (MMw > or = 2000). Radiostrontium is present principally in the fraction of inorganic compounds (19-100%) and in the low molecular mass fraction of organic matter (MMw = 350-500). A selective interaction of 137Cs with organic matter of definite molecular masses was not observed. The radionuclide was found in the "organic" fractions of a wide range of molecular masses (MMw from 350-500 to > or = 18,000) (34-97%) as well as in the fraction of inorganic compounds. The data obtained can provide the theoretical basis for explanation of higher mobility of 90Sr in soil profiles compared to other radionuclides.     

Association of Chernobyl-derived 239+240Pu, 241Am, 90Sr and 137Cs with different molecular size fractions of organic matter in the soil solution of two grassland soils

Radiocesium is normally bound only rather weakly and unspecifically by humic substances, in contrast to the actinides Pu and Am. Recently, however, it was observed that fallout ¹³⁷Cs in the soil solution from an Of-horizon of a podzol forest soil (slightly decomposed plant material) was associated essentially only with one single size fraction of the humic substances. In deeper soil layers with well humified material (AOh-horizon), radiocesium was associated with all size fractions of the dissolved organic matter (DOM). To examine whether this unexpected behaviour is also observable for DOM isolated from other soils, we determined the association of fallout ¹³⁷Cs,⁹⁰Sr,²³⁸Pu, ^239+240Pu and ²⁴¹Am with various size fractions of DOM from in situ soil solutions isolated from two layers (0–2 cm and 2–5 cm) of two grassland soils (a soddy podzolic soil and a peat soil) within the 10 km zone of the nuclear reactor at Chernobyl (Ukraine). The four size fractions of DOM as obtained by gel filtration of the soil solution were (mean nominal molecular weight in daltons): fraction I: ≥2000, fraction II: 1300; fraction III: 560, fraction IV: inorganic compounds. The results for the well humified DOM (humus accumulation horizon of podzol, deeper layer of peat soil) showed that Pu and Am are essentially associated with the high molecular weight fractions, while Sr is present only in the `inorganic' fraction. Radiocesium is found in all the size fractions separated. A quite similar pattern was also found for Pu, Am, and Sr in the soil solution from only slightly decomposed plant material (0–2 cm of peat soil), but not for radiocesium. This radionuclide was again essentially only observable in one single low molecular weight fraction of DOM. The above results thus support our recent observations in the different horizons of a forest podzol mentioned above, even though no reason for the different binding of radiocesium by well humified soil organic matter and by only slightly decomposed plant material can be given at present. The data demonstrate, however, that information on only the total amount of a radionuclide in the soil solution will not be sufficient to interpret or predict its fate adequately in the soil. Received: 13 February 1998 / Accepted in revised form: 14 July 1998     

Estimation of rate constant for dissolution of radioactive fuel particles

Some theoretical of the experimental investigation of solubility of radioactive aerosols were examined. Filters, which were exposed during October-November 1987 in Pripyat town, were studied. Measurements on 22 November 1987 showed that an activity in the air was 12.1-20.8 mBq/m3 for 137Cs, 34.9-89.3 mBq/m-3 for 144Ce, 24.3-30.5 mBq/m-3 for 106Ru. Disperse structure of aerosol hot particles and the number of hot particles on each filter fragment was estimated by radiography. To determine a dissolution rate constant a static system with two 0.14 micron pore size membrane MFE filters (Dubna, Russia) enclosing fragments of Petryanov filters was selected. The composition was held in Gamble's solution lung fluid anf then in 0.1 mol/l HCl as dastic juice simulation. The activity of 90Sr, 238Pu, 239 + 240Pu, 241Am and 244Cm in aerosol filters and solutions was measured by radiochemical methods. It was shown that leaching of radionuclides from aerosol hot particles in lung fluid simulation decreases in line 137Cs > 90Sr > 239 + 240Pu > or = 241Am, depending om particle diameter and time. Dissolution constants were presented. Dissolution of aerosol particles in 0.1 mol/l HCl is also shown (dissolution time was 3 days). A radionuclide transition to HCl solution decreases in line 90Am 241Am > 137Cs > 239 + 240Pu. A transition degree reached 21% for 90Sr and extraction of 241Am was 3-17%.     

The use of fallout 137Cs and 239,240Pu for dating of lake sediments

The distribution of ¹³⁷Cs and ^239,240Pu in sediment core samples of the Finnish lakes Laukunlampi, Lovojärvi and Pääjärvi were determined. The sediment samples were collected using dry ice and liquid nitrogen freezing methods. The sediments of these lakes are annually laminated. A clear maximum concentration of ¹³⁷Cs and ^239,240Pu was found in sediment layers formed during 1962–1964, the years of maximum fallout, and the middle of the 1950's can be estimated from the ¹³⁷Cs and ^239,240Pu profiles. The highest concentrations, 11 500 and 820 pCi kg^–1 dry wt for ¹³⁷Cs and ^239,240Pu, respectively, were found in the sediment of Laukunlampi. The vertical distribution was similar for ¹³⁷Cs and ^239,240Pu in the lakes investigated. A slight migration of ^239,240Pu and ¹³⁷Cs was found and the migration of ¹³⁷Cs seems to be higher than that of ^239,240Pu. The advantages of ¹³⁷Cs dating method are rapidity and simplicity. ^239,240Pu is preferable when the sample size is small. The agreement found between ¹³⁷Cs and ^239,240Pu dates and the annual laminae show that these fallout radio isotopes can be used for dating sediments formed during the past 25 years.     

<Superscript>137</Superscript>Cs, <Superscript>40</Superscript>K, <Superscript>238</Superscript>Pu, <Superscript>239+240</Superscript>Pu and <Superscript>90</Superscript>Sr in biological samples from King George Island (Southern Shetlands) in Antarctica

There are few data reported on radionuclide contamination in Antarctica. The aim of this paper is to report ¹³⁷Cs, ⁹⁰Sr and ^238,239+240Pu and ⁴⁰K activity concentrations measured in biological samples collected from King George Island (Southern Shetlands, Antarctica), mostly during 2001–2002. The samples included: bones, eggshells and feathers of penguin Pygoscelis papua, bones and feathers of petrel Daption capense, bones and fur of seal Mirounga leonina, algae Himantothallus grandifolius, Desmarestia anceps and Cystosphaera jacquinotii, fish Notothenia corriceps, sea invertebrates Amphipoda, shells of limpet Nacella concina, lichen Usnea aurantiaco-atra, vascular plants Deschampsia antarctica and Colobanthus quitensis, fungi Omphalina pyxidata, moss Sanionia uncinata and soil. The results show a large variation in some activity concentrations. Samples from the marine environment had lower contamination levels than those from terrestrial ecosystems. The highest activity concentrations for all radionuclides were found in lichen and, to a lesser extent, in mosses, probably because lichens take up atmospheric pollutants and retain them. The only significant correlation (except for that expected between ²³⁸Pu and ^239+240Pu) was noted for moss and lichen samples between plutonium and ⁹⁰Sr. A tendency to a slow decrease with time seems to be occurring. Analyses of the activity ratios show varying fractionation between various radionuclides in different organisms. Algae were relatively more highly contaminated with plutonium and radiostrontium, and depleted with radiocesium. Feathers had the lowest plutonium concentrations. Radiostrontium and, to a lesser extent, Pu accumulated in bones. The present low intensity of fallout in Antarctic has a lower ²³⁸Pu/^239+240Pu activity ratio than that expected for global fallout.     

Radioactive aerosols released from the Chernobyl Shelter into the immediate environment

The release of radioactive particles through large gaps in the containment of the destroyed Chernobyl reactor was assessed during two measurement periods. In 1996–1999, a total radionuclide flow rate of 274 Bq s⁻¹ or 8.64 × 10⁹ Bq year⁻¹ was determined. These releases were predominantly due to ¹³⁷Cs (78.5%), ⁹⁰Sr (21.1%), and ^239+240Pu (0.4%). The mean activity concentration in the aerosol measured directly at the gaps was about 240 mBq m⁻³ with an activity median aerodynamic diameter (AMAD) of 2.4 μm for ¹³⁷Cs, 120 mBq m⁻³ with an AMAD in the range 3.1–13 μm for ⁹⁰Sr, 1.8 mBq m⁻³ with an AMAD in the range 3.5–11 μm for ^239+240Pu, and 2.0 mBq m⁻³ with an AMAD of 1.5 μm for ²⁴¹Am. The resulting total inhalation dose rate calculated close to the gaps was about 100 nSv h⁻¹. In the near environment, the mean ¹³⁷Cs activity in the aerosol was 2.2 mBq m⁻³ with an AMAD of 2.2 μm, which gave rise to an inhalation dose rate of about two orders of magnitude lower than the corresponding dose rate at the gaps. Occasionally, however, dose levels were measured in the near environment that were similar to those at the gaps. In 2000–2003, lower activity concentrations were observed. The decrease was more pronounced at the gaps than in the near environment. The results indicate that effective dose due to inhalation must be considered for the dose assessment of construction workers who will be deployed at the Chernobyl site to reconstruct the old or to build the new Shelter, in the future.     

Caesium-137 profiles in the sediments of a partial-meromictic lake on Great Sandy Island (Fraser Island), Queensland,Australia

Hidden Lake is a perched, brown-water lake located in the centre of Great Sandy Island (Fraser Is.), S.E. Queensland. It is highly acid (pH 4.0), oligotrophic and is thermally and chemically stratified for most of the year. The sediments revealed a ¹³⁷Cs profile which departed from the temporal pattern of ¹³⁷Cs fallout in Brisbane and was represented by an exponential increase of ¹³⁷Cs towards the surface sediments from ca. 32 cm depth. The possible causes of the divergent profile are discussed, including physical and biological mixing, lag in the transport of catchment material to the sedimentary basin, diffusion, recycling and biological concentration. It is hypothesised that a combination of the last four processes, with diffusion facilitated by the highly acid conditions, are the major causes of the observed ¹³⁷Cs profile. Possible recycling and bioconcentration of ¹³⁷Cs raises questions as to the validity of this method of dating in similar environmental conditions, and as to the interpretation of other palaeochemical data. These hypotheses are to be tested against profiles obtained from ¹⁴C, ²¹⁰Pb, ^239/240Pu analyses of the sediment, and the measurement of ¹³⁷Cs activity in the water and biota of the lake.     

Influence of clay mineral type and organic matter content on the uptake of239Pu and241Am by plants

Summary The uptake of²³⁹Pu and²⁴¹Am from different clay mineral-organic matter-sand mixtures simulating contrasting soil types was examined in growth chamber experiments. The mixtures represented various combinations of organic matter (0, 5 and 10%), kaolinite (11 type) and montomorillonite (21 type) clay minerals, each at the levels of 5, 10 and 25%, and purified quartz sand (as filler).Results indicated a marked reduction in uptake of both²³⁹Pu and²⁴¹Am with increase in organic matter as well as clay content of the mixtures. The Pu Concentration Ratios (CRs) ranged from (2.5–7.0)×10^–3 in the case of kaolinite-organic matter mixtures, and from (0.9–5.5)×10^–3 in the case of montmorillonite-organic matter mixtures. The corresponding values of Am Concentration Ratios (CRs) obtained were (1.9–725.4)×10^–3 in the case of kaolinite-organic matter mixtures, and between (0.7–3.5)×10^–3 for the montmorillonite-organic matter mixtures.Reduction in the uptake of²⁴¹Am with increasing clay content was more pronounced in the montmorillonite clay-organic matter mixtures as compared to that in the case of kaolinite-organic matter mixtures. While similar qualitative reduction in²³⁹Pu CRs with increasing clay content was observed, the reduction was less marked than in the case of²⁴¹Am. The values for Am CRs were higher than the corresponding Pu CRs in kaolinite based mixtures whereas in the case of montmorillonite-organic matter mixtures Pu CRs exceeded the Am CRs.Increasing organic matter content and its interaction with both kaolinite and montmorillonite clay minerals were found to be equally effective in reducing the uptake of²³⁹Pu as well as²⁴¹Am by plants.     

Reconstruction of local fallout composition and gamma-ray exposure in a village contaminated by the first USSR nuclear test in the Semipalatinsk nuclear test site in Kazakhstan

After the disintegration of the USSR in end of 1991, it became possible for foreign scientists to visit Kazakhstan, in order to investigate the radiological consequences of nuclear explosions that had been conducted at the Semipalatinsk nuclear test site (SNTS). Since the first visit in 1994, our group has been continuing expeditions for soil sampling at various areas around SNTS. The current level of local fallout at SNTS was studied through γ-spectrometry for ¹³⁷Cs as well as α-spectrometry for ^239,240Pu. Average values of soil inventory from wide areas around SNTS were 3,500 and 3,700 Bq m^?2 for ¹³⁷Cs and ^239,240Pu, respectively, as of January 1, 2000. The average level of ¹³⁷Cs is comparable to that in Japan due to global fallout, while the level of ^239,240Pu is several tens of times larger than that in Japan. Areas of strong contamination were found along the trajectories of radioactive fallout, information on which was declassified after the collapse of the USSR. Our recent efforts of soil sampling were concentrated on the area around the Dolon village heavily affected by the radioactive plume from the first USSR atomic bomb test in 1949 and located 110 km east from ground zero of the explosion. Using soil inventory data, retrospective dosimetry was attempted by reconstructing γ-ray exposure from fission product nuclides deposited on the ground. Adopting representative parameters for the initial ¹³⁷Cs deposition (13 kBq m^?2), the refractory/volatile deposition ratio (3.8) and the plume arrival time after explosion (2.5 h), an absorbed dose in air of 600 mGy was obtained for the 1-year cumulative dose in Dolon village, due to the first bomb test in 1949. Considering possible ranges of the parameters, 350 and 910 mGy were estimated for high and low cases of γ-ray dose in air, respectively. It was encouraging that the deduced value was consistent with other estimations using thermal luminescence and archived monitoring data. The present method can be applied to other settlements affected by local fallout from SNTS.     

Potential for phytoextraction of137 Cs from a contaminated soil

Potential for phytoremediation of a soil contaminated with radiocesium was investigated in three phases: (1) hydroponic screening for plant species capable of accumulating elevated levels of cesium in shoots, (2) investigation of several amendments for their potential to increase the bioavailability of ¹³⁷Cs in the contaminated soil, and (3) bioaccumulation of radiocesium in shoots of plants grown in¹³⁷ Cs-contaminated soil.The bioaccumulation ratio for Cs in shoots of hydroponically grown plants ranged between 38 and 165. From solution, dicot species accumulated 2- to 4-fold more cesium in shoots than grasses. In studies investigating the bioavailability of ¹³⁷Cs in aged contaminated soil, ammonium salts were found to be the most effective desorbing agents, releasing approximately 25% of the¹³⁷ Cs. The extent of ¹³⁷Cs desorption from the soil increased with ammonium concentration up to 0.2 M. In a pot study conducted in a greenhouse, there was significant species-dependent variability in the ability to accumulate ¹³⁷Cs in the shoot from contaminated soil. The ability to accumulate ¹³⁷Cs from the soil increased in the order: reed canarygrass (Phalaris arundinacea) < Indian mustard (Brassica juncea) < tepary bean (Phaseolus acutifolius)< cabbage (B. oleracea var. capitata). It was also found that addition of NH₄NO₃ solution to the soil elicited a two- to twelve-fold increase in ¹³⁷Cs accumulation in the shoot. The greatest amount of ¹³⁷Cs (40 Bq g^-1 dw) was removed in shoots of cabbage grown in contaminated soil amended with 80 mmols NH₄NO₃ kg^-1 soil. Bioaccumulation ratios of 2–3 were obtained with the best performing plant species. These values are significantly greater than those previously reported in the literature (usually <0.1) for plants grown on aged contaminated soil. These results indicate that careful species selection along with amendments that increase the bioavailability of¹³⁷ Cs in the soil could greatly enhance the prospects for the use of plants to remediate ¹³⁷Cs-contaminated soils.     

90Sr, 137Cs, 238Pu, 239+240Pu,and 241Am radionuclides in macrophytes within the Krasnensky flood plain: species specificity of concentration and distribution in phytocenosis components

The analysis of the content of radionuclides 90Sr, 137Cs, 238Pu, 239 + 240Pu and 241Am in water vegetation of flood plain reservoirs has allowed studing features of radionuclide accumulation by various species of macrophytes and revealing bioindicators of radionuclide contamination. Thus species-specificity of radionuclide accumulation can essentially change the contribution of different species to a percentage ratio of the radionuclide content in phytomass of reservoirs in comparison with fund of higher aquatic plants.     

Relations between resuspension and the content of 137Cs in freshwater fish in some Swedish lakes

In many Swedish lakes, the fallout of ¹³⁷Cs from the Chernobyl accident in April 1986 has largely accumulated in the sediments. The availability and transfer of deposited ¹³⁷Cs to biota is influenced by factors such as resuspension. The frequency of resuspension and the ¹³⁷Cs-content of different fish species was studied in three shallow lakes in Uppland, central Sweden, and in one deeper lake in northern Sweden. Resuspension was measured by the use of sediment traps. Sedimentation rates measured from the traps in the shallower lakes were 5–10 times higher than normal for this type of lake, indicating that resuspension was an important factor. The decrease of the ¹³⁷Cs-content in muscle tissue of pike, perch and roach was slow in each of the shallow lakes. ¹³⁷Cs decreased by about 30% over a period of 2 years in the shallowest lake (maximum depth 4 m), whereas ¹³⁷Cs decreased by 50% in the deeper lakes (maximum depth 10 m). The slower rates of decline of ¹³⁷Cs in biota from the shallow lakes, are probably a function of sediment dynamics (mainly influenced by lake morphometry, wind direction and strength). They may be influenced, also, by bioavailability of resuspended sediment material. In the deepest northern lake, much of the ¹³⁷Cs-containing material collected in the sediment traps originated from the catchment area. Resuspension was minimal, and the high activity of ¹³⁷Cs in the sediment had no effect on content or decline of ¹³⁷Cs in lake fish.     

Variability of water content and of depth profiles of global fallout 137Cs in grassland soils and the resulting external gamma-dose rates

¹³⁷Cs from global fallout of nuclear weapon testings in the 1950s and 1960s was determined in successive layers (0–30 cm) of eight undisturbed grassland soils in Bavaria, Germany. The maximum activity concentration was found in soil layers between 4 and 15 cm below the surface. Using the vertical distribution of the cesium activity, which varied considerably from site to site, the mean residence half-time of ¹³⁷Cs from global fallout in each soil layer was evaluated with a compartment model. These values ranged from 1.0 to 6.3 years/cm. The mean residence half-time averaged over all soil layers and all sites was 2.7±1.4 years/cm and, thus, about twice the corresponding residence half-time of the Chernobyl-derived ¹³⁷Cs as determined in the same soil layers (also in 1993). The dose rate of the external gamma-radiation due to ¹³⁷Cs from global fallout in the soil determined from the depth distributions varied between 0.34 and 0.57 (mean: 0.45±0.07) nGy/h per kBq/m². The effect of soil water content on the dose rate was studied by considering four states of the soil, from water content zero to complete water saturation of the total pore volume. It was shown that the difference between the dose rates at the permanent wilting point and the field capacity, which both represent the most relevant water contents of soils, was only 10% of the dose rate at the permanent wilting point for all sites. Received: 8 September 1997 / Accepted in revised form: 15 December 1997     

Response of changes in soil nutrients to soil erosion on a purple soil of cultivated sloping land

Severe soil erosion of cultivated sloping land in hilly areas of Sichuan, China, has resulted in deterioration of soil quality, and therefore has an adverse impact on crop production. A hillslope of 110 m in length was selected with a slope steepness of 10.12% where the soils were classified as Regosols. Soil samples for determining ¹³⁷Cs, soil organic matter (SOM), total N, P, K, available N, P, K and particle size fraction were collected at 10 m intervals along a transect of the hillslope. Loss of soil nutrients owing to soil erosion was studied by using ¹³⁷Cs technique, and the relationships between ¹³⁷Cs-derived soil redistribution rates and soil nutrients were established over the cultivated sloping land in hilly areas of Sichuan, China (30o26′N, 104o28′E). The values of SOM, total N, available N, P, K and the soil particle fractions of size < 0.002 mm were smaller at upper and middle slope positions where ¹³⁷Cs inventories were lower (i.e., soil erosion rates were higher) than at downslope positions where ¹³⁷Cs inventories were higher (i.e., soil erosion rates were lower). The lowest ¹³⁷Cs inventories were found at the hilltop, showing that besides erosion owing to water flow, tillage also contributed to soil losses, and intensive tillage was mostly responsible for severe erosion at upper slope positions. There were significant differences in SOM, total N, available N, P, K and the soil particle fractions of size < 0.002 mm between different slope segments, and these properties were significantly correlated with slope length. These soil properties were also significantly correlated with ¹³⁷Cs inventories, indicating that both ¹³⁷Cs and nutrient concentrations varied with topographical changes. The variation in soil properties was strongly influenced by erosion-induced soil redistribution, and therefore ¹³⁷Cs inventories mirroring soil redistribution rates would be considered as an integrated indicator of soil quality.     

Carbon and nitrogen stocks in physical fractions of a subtropical Acrisol as influenced by long-term no-till cropping systems and N fertilisation

The long-term soil management effects on C and N stocks of soil physical fractions are still poorly understood for South American subtropical soils. This study aimed (i) to evaluate the influence of cereal- and legume-based cropping systems and N fertilisation on C and N stocks of the sand-, silt- and clay-size fractions of a no-tilled subtropical Acrisol in southern Brazil, (ii) to compute the Carbon Management Index (CMI) for those cropping systems using physical fractionation data, and (iii) to investigate the possible existence of finite capacity of those soil physical fractions to store C and N. Soil samples of a long-term experiment were collected from the 0–2.5 and 2.5–7.5 cm layers of three no-till cropping systems [fallow bare soil, oat/maize (O/M) and pigeon pea+maize (P+M)] under two N fertilisation levels (0 and 180 kg N ha^–1). However, for fallow bare soil, only the non-fertilised sub-plot was sampled. An adjacent native grassland soil was sampled as a reference. The C and N stocks of the three soil physical fractions were higher in the legume-based cropping system (P+M) than in O/M and bare soil, because of the higher residue input in the former. The P+M cropping system restored the C and N stocks in sand- and silt-size fractions to the same levels found in grassland soil. Higher C and N stocks in all physical fractions were also obtained with N fertilisation. The C and N stocks and the C:N ratio were most affected by cropping systems in the sand- and least in the clay-size fraction. Particulate organic matter was found in the silt-size fraction, showing this fraction is not only constituted by mineral-associated organic mater, as commonly believed. Taking grassland soil as reference (CMI = 100), the CMI ranged from 46, in O/M no N, to 517, in P+M with N, pointing to a better soil management in the latter. The clay-size fraction tended to show a finite capacity to store C and N (48.8 g C kg^–1 and 4.9 g N kg^–1 of clay), which was not verified in sand- and silt-size fractions. The adoption of no-tillage and legume-based cropping systems with high residue input are adequate soil management strategies to improve soil quality and make the agricultural production systems more sustainable in subtropical regions.     

The distribution of the radionuclides in the main components of lake ecosystems within the Chernobyl NPP exclusion zone

The results of the studies devoted to the distribution of radionuclides 90Sr, 137Cs, 238Pu, 239 + 240Pu and 241Am in 1998-2003 in main components of Glubokoe Lake and Dalekoe-1 Lake located within Krasnensky flood lands of the Pripyat River (inner exclusion zone of the Chernobyl NPP) were analysed. The data about the radionuclide content in bottom sediments, in water, in seston, in macrozoobenthos (including bivalvia molluscs), in gasteropods molluscs, in higher aquatic plants and in fish are presented.     

Natural and Chernobyl-caused radioactivity in mushrooms,mosses and soil-samples of defined biotops in SW Bavaria

Summary Different mushrooms, mosses and corresponding soil samples have been collected mainly from two sites in the alpine region of southwestern Bavaria. At the end of the growthseason, September 1986, gamma spectroscopic analysis showed that the moss-, mould, and needle-layer contained considerably more ¹³⁴Cs and ¹³⁷Cs activity per unit fresh weight than eight different species of mushroom. These two isotopes were carried into the biotop mainly as a consequence of the Chernobyl accident. ¹³¹J could not be found any more in the samples ca. 5–6 months after the catastrophe. The activity of the cesium isotopes decreased with increasing soil depth. In the mushrooms the activity was relatively high in Xerocomus badius and surprisingly low in Boletus edulis; samples of the latter and of Cantharellus cibarius collected in September 1985 (before the accident) and kept deep frozen contained almost identical amounts of ¹³⁷Cs as those collected from August to October 1986. Mushrooms contained considerably more of the natural isotope ⁴⁰K than the needlelayers and the soil samples in the neighbourhood. In all mushrooms except Xerocomus badius the activity of ⁴⁰K was generally higher than the ¹³⁷Cs activity. The results indicate that except Xerocomus badius the analyzed mushrooms do not actively take up Cs from the soil, in contrast to K.