Influence of rainfall characteristics on elimination of aerosols of cesium, strontium, barium and tellurium deposited on grassland

This work is aimed at quantifying foliar transfer of cesium, strontium, barium and tellurium under the influence of rainfall characteristics (intensity, frequency and time elapsed between contamination and first rainfall). Grassland boxes were contaminated by dry deposition of multi-element aerosols of (137)Cs, (85)Sr, (133)Ba and (123m)Te. They were grown in a greenhouse under controlled conditions. The treatments consisted of mowing and applying rainfalls (8 and 30 mmh(-1)) at different times after the contamination. At a leaf area index of 5.9+/-1.9, interception of the aerosols was similar for the 4 radionuclides (83.8+/-5.9%). Dew produced significant radionuclide accumulation in the base of the vegetation and transfer to the soil. For moderate intensity, an early (2 days after contamination) first rainfall was as efficient, in terms of leaf wash-off, as a longer rainfall occurring later (6 days after contamination). For early rainfalls, eliminated activities were comparable because the influence of rain intensity was compensated by rain duration. However, for late rainfalls, wash-off efficiency increased with rainfall intensity. Total transfer factors (TTF) were determined on whole grass immediately after 4 rainfalls and at harvest. After 4 medium intensity rainfalls, rain frequency did not influence total transfer factors (TTF) of strontium, barium and tellurium (about 0.2, 0.3 and 0.35 Bq kg(fresh weight)(-1) by Bq m(-2), respectively). Cesium TTF value was lower in the case of a weekly rain (0.1 against 0.2 Bq kg(fresh weight)(-1) by Bqm(-2)). TTF values were similar for twice-a-week rainfalls, whatever their intensity. They were higher for weekly rains of high intensity (between 0.3 and 0.75 Bq kg(fresh weight)(-1) by Bqm(-2) against 0.1-0.35 Bq kg(fresh weight)(-1) by Bq m(-2), depending on the radionuclides). TTF values attested that wash-off was more efficient when rainfalls lasted longer. Field loss on the top of the leaves was well described by an offset exponential model. The half-lives varied with rainfall characteristics from 4 days for cesium, strontium and barium to 20 days for tellurium. The offset value varied between 0% for tellurium (high intensity rainfalls) and 14% for cesium (medium intensity rainfalls).     

Watershed wash-off of atmospherically deposited radionuclides: review of the fluxes and their evolution with time

Radionuclide transport with water from contaminated watersheds is an intermittent flux--also called watershed wash-off--which causes radionuclide redistribution in terrestrial ecosystems, and more critically radionuclide delivery to downstream waterbodies. Mean wash-off fluxes and their evolution with time have been generally quantified with transfer functions, which can be seen as transfer factors varying with time. But unfortunately the published quantifications rely on many analytical formulations for the transfer function. This paper aims at unifying the heterogeneous information concerning radionuclide wash-off. A generic transfer function model was proposed. Published wash-off quantifications were gathered in a database and converted within this new framework. This extensive review covered various radionuclides, source terms, processes, time and space scales reported in the literature since 1960. It demonstrated the feasibility of a generic wash-off model. Intervals of variations for the introduced coefficients were summarised and the influence of wash-off conditions were discussed. In some cases, the influence of wash-off conditions should be clarified to propose narrower parameter intervals for practical assessments.     

Seasonal variations in radionuclide transfer in a Mediterranean grazing-land ecosystem.

We made quarterly determinations of the transfer coefficients and effective transfer coefficients for the radionuclides 137Cs, 90Sr, 40K, 226Ra, 228Ra and 228Th over a full annual cycle, in a Mediterranean grazing-land ecosystem. The input and output fluxes of the radionuclides between the different compartments of this ecosystem were quantified for the following processes: root uptake; variation in root and aerial biomass; pasture production; translocation; leaf fall; efflux due to grazing action; resuspension and subsequent aerial deposition of radionuclides. We observed there to be a marked seasonal variation for this type of ecosystem in both the transfer coefficients and the radionuclide fluxes, which impedes the soil-plant transfer being characterized on the basis of values that are constant with time.     

Foliar and root uptake of 134Cs, 85Sr and 65Zn in processing tomato plants (Lycopersicon esculentum Mill.)

Rice is a staple food in Japan and other Asian countries, and the soil-to-plant transfer factor of 137Cs released into the environment is an important parameter for estimating the internal radiation dose from food ingestion. Soil and rice grain samples were collected from 20 paddy fields throughout Aomori Prefecture, Japan in 1996 and 1997, and soil-to-polished rice transfer factors were determined. The concentrations of 137Cs, derived from fallout depositions, stable Cs and K in paddy soils were 2.5-21 Bq kg(-1), 1.2-5.3 and 5000-13000 mg kg(-1), respectively. The ranges of 137Cs, stable Cs and K concentration in polished rice were 2.5-85 mBq kg(-1) dry wt., 0.0005-0.0065 and 580-910 mg kg(-1) dry wt., respectively. The geometric mean of soil-to-polished rice transfer factor of 137Cs was 0.0016, and its 95% confidence interval was 0.00021-0.012. The transfer factor of 137Cs was approximately 3 times higher than that of stable Cs at 0.00056, and they were well correlated. This implied that fallout 137Cs, mostly deposited up to the 1980s, is more mobile and more easily absorbed by plants than stable Cs in the soil, although the soil-to-plant transfer of stable Cs can be used for predicting the long-term transfer of 137Cs. The transfer factors of both 137Cs and stable Cs decreased with increasing K concentration in the soil. This suggests that K in the soil was a competitive factor for the transfers of both 137Cs and stable Cs from soil-to-polished rice. However, the transfer factors of 137Cs and stable Cs were independent of the amount of organic materials in soils.     

Altitude dependent 137Cs concentrations in different plant species in alpine agricultural areas

The Gastein valley in the Central Part of the Austrian Alps was one of the regions most heavily affected by fallout of the Chernobyl nuclear catastrophe, depositing (137)Cs inventory up to 70 kBq/m(2) in May 1986. In many studies dealing with the uptake of (137)Cs by vegetation used for farming, a significant correlation between (137)Cs concentration in the plants and altitude a.s.l. has been observed. In order to quantify the influence of the composition of plant communities on the average (137)Cs concentration in vegetation on farmland, plant-specific activity concentrations in plant species have been determined. Alongside a transect from valley sites at 850 m a.s.l. to alpine pastures at 1660 m, the aggregated transfer factors C(ag) (m(2)/kg) have been measured for plant communities and plant species. C(ag) values for mixed vegetation are more or less similar in valley sites, but they increase exponentially with a doubling height of 122+/-22 m above appr. 1200 m altitude a.s.l. On average all species are affected by this increase in a similar way. C(ag) values of ubiquitous plant indicate that the composition of plant communities is of minor importance for the contamination of mixed vegetation.     

A modelling study on 137Cs and 239,240Pu behaviour in the Alborán Sea, western Mediterranean

A model for simulating the dispersion processes of 137Cs and 239,240Pu in the Alborán Sea is described. The model consists of two hydrodynamic models: a 2D depth-averaged model and a two-layer model which provide tidal and geostrophic currents, respectively; a sediment transport model which provides suspended particle concentrations and sedimentation rates over the domain; and the radionuclide dispersion model including interactions of dissolved radionuclides with suspended particles and bed sediments. These processes are formulated using kinetic transfer coefficients. The hydrodynamic and sediment models are run and validated in advance, and their results are then used to simulate the dispersion of 137Cs and 239,240Pu, which are introduced from atmospheric fallout. Radionuclide concentrations in the water column and distributions in bed sediments have been compared with measurements in the sea. Both set of data are, in general, in agreement. The model has also been applied to calculate radionuclide fluxes through the Strait of Gibraltar. These computed fluxes have been compared with previous estimations as well.     

Inventories of fallout 210Pb and 137Cs radionuclides in moorland and woodland soils around Edinburgh urban area (UK)

Inventories of fallout (210)Pb and (137)Cs have been measured in moorland and woodland soils around the Edinburgh urban area, using a high purity germanium detector. The (210)Pb inventories in moorland soils were relatively uniform, with a mean value of 2520+/-270Bqm(-2). The mean (137)Cs inventory in moorland soils varied greatly from 1310 to 2100Bqm(-2), with a mean value of 1580+/-310Bqm(-2). The variability was ascribed mainly to the non-uniform distribution of fallout Chernobyl (137)Cs. The mean (210)Pb and (137)Cs inventories in woodland canopy soils were found to be 3630+/-380Bqm(-2) and 2510+/-510Bqm(-2), respectively. At sites for which both moorland and woodland data were available, the mean inventories provided fairly similar average enhancements of (47+/-7)% and (46+/-18)% of (210)Pb and (137)Cs under woodland canopy soils relative to open grassland soils, respectively. The enhancement factors are broadly in line with other independent findings in literature. Enhancement of both (210)Pb and (137)Cs in woodland soils relative to moorland soils is, in part, due to deposition by impaction during air turbulence, wash-off, gravitational settling and deposition during leaf senescence. Results of this study suggest that these processes affect both (210)Pb and (137)Cs carrier aerosols in a similar way.     

A new general dynamic model predicting radionuclide concentrations and fluxes in coastal areas from readily accessible driving variables

This paper presents a general, process-based dynamic model for coastal areas for radionuclides (metals, organics and nutrients) from both single pulse fallout and continuous deposition. The model gives radionuclide concentrations in water (total, dissolved and particulate phases and concentrations in sediments and fish) for entire defined coastal areas. The model gives monthly variations. It accounts for inflow from tributaries, direct fallout to the coastal area, internal fluxes (sedimentation, resuspension, diffusion, burial, mixing and biouptake and retention in fish) and fluxes to and from the sea outside the defined coastal area and/or adjacent coastal areas. The fluxes of water and substances between the sea and the coastal area are differentiated into three categories of coast types: (i) areas where the water exchange is regulated by tidal effects; (ii) open coastal areas where the water exchange is regulated by coastal currents; and (iii) semi-enclosed archipelago coasts. The coastal model gives the fluxes to and from the following four abiotic compartments: surface water, deep water, ET areas (i.e., areas where fine sediment erosion and transport processes dominate the bottom dynamic conditions and resuspension appears) and A-areas (i.e., areas of continuous fine sediment accumulation). Criteria to define the boundaries for the given coastal area towards the sea, and to define whether a coastal area is open or closed are given in operational terms. The model is simple to apply since all driving variables may be readily accessed from maps and standard monitoring programs. The driving variables are: latitude, catchment area, mean annual precipitation, fallout and month of fallout and parameters expressing coastal size and form as determined from, e.g., digitized bathymetric maps using a GIS program. Selected results: the predictions of radionuclide concentrations in water and fish largely depend on two factors, the concentration in the sea outside the given coastal area and/or adjacent coastal areas and the ecological half-life of the radionuclide in the sea. Uncertainties in these factors generally dominate all other uncertainties, e.g., concerning the surface water retention time, the settling velocity of the particulate fraction, the distribution coefficient regulating the fluxes in dissolved and particulate phases, the catchment area influences and the factors regulating biouptake and excretion of the radionuclide in fish. This means that the conditions in the sea are of paramount importance for the conditions in the coastal area, even for relatively enclosed coastal areas. This coastal model may be regarded as a tool for testing working hypotheses on the relative roles of different processes in different coastal areas. Such information is essential for getting realistic expectations of various remedial measures, such as coastal dredging discussed in this work.     

A new generic sub-model for radionuclide fixation in large catchments from continuous and single-pulse fallouts, as used in a river model

This paper presents a new general sub-model for fixation in catchment areas to be used within the framework of a river model for substances such as radionuclides and metals from continuous and single-pulse fallouts. The model has been critically tested using data from 27 European river sites covering a very wide geographical area and contaminated by radiocesium and radiostrontium from the Chernobyl accident and from the nuclear weapons tests (NWT fallout). This modelling approach gives radionuclide concentrations in water (total, dissolved and particulate phases) at defined sites on a monthly basis. The overall river model is based on processes in the upstream river stretch and in the catchment area. The catchment area is differentiated into inflow (approximately dry land) areas and outflow (approximately wetland) areas. The model has a general structure, which can be used for all radionuclides or substances. It is simple to apply in practice since all driving variables may be readily accessed from maps and standard monitoring programs. The driving variables are: latitude, altitude, catchment area, mean annual precipitation and fallout. Note that for large catchments, this model does not require data on the characteristic soil type or the percentage of outflow areas (wet lands) in the catchment, as in most previous models, since in practice it is very difficult to obtain reliable data on characteristic soil type or percentage of outflow areas, especially in large and topographically complex catchments. Modelled values have been compared to empirical data from rivers sites covering a wide domain (catchment areas from 3000 to 3,000,000 km2, precipitation from 400 to 1700 mm/year; fallouts from 1600 to 280,000 Bq/m2; altitudes from 0 to 1000 m.a.s.l. and latitudes from 41 degrees to 72 degrees N). The river model with its sub-model for fixation predicts close to the uncertainty factors given by the empirical data, which have been shown to be about a factor of 1.6 for 137Cs and a factor of 2.2 for 90Sr in river water. The obtained characteristic uncertainty factors for 137Cs from the Chernobyl fallout is 2.4, for 137Cs from the NWT fallout it is 1.3 and for the 90Sr results from the NWT fallout it is 3 using the new model.     

The radiological impact of the Chernobyl debris compared with that from nuclear weapons fallout

Our basic knowledge of the radiological impact of fallout from nuclear accidents is based on the experience gained from the study of nuclear weapons fallout. Radioecologically, the most important radionuclides generated by the Chernobyl accident were ¹³⁷Cs, ¹³⁴Cs, ¹³¹I and, to a lesser degree, ⁹⁰Sr. These nuclides are well known from global fallout, although in different relative amounts to those observed in the Chernobyl debris. Another important difference between the fallout from Chernobyl and that from nuclear weapon tests is that their seasonal and geographical distributions were quite dissimilar. A number of examples show how these differences influenced transfer factors and thus population doses. Special emphasis is paid to the contamination of milk and cereal products.Furthermore, it is shown how the composition of the Chernobyl debris changed with distance from Chernobyl, due to the differences in volatility of the various radionuclides involved. Finally, the paper compares the dose equivalents received from unit releases (1 P Bq ¹³⁷Cs) of global fallout and of Chernobyl accident debris.     

Influence of spruce and pine on the acidity and composition of atmospheric fallout in north taiga forests of an industrially developed region

The ideas concerning the spatial and temporal variation of acidity and composition of atmospheric fallout in forests of the boreal zone are discussed. The role played by the atmospheric component in the functioning of these forests depends on the acidity and composition of fallout and the extent of their transformation by the biocenosis. The most profound transformation of fallout occurs during the growing season. In spaces between crowns, the corresponding changes are atmogenic; in undercrown areas, they are obviously biogenic (autogenic). Spruce transforms the fallout more intensively than pine. Under conditions of industrial pollution, the atmobiogenic character of fallout is supplemented with a technogenic component, as its acidity and concentration of pollutants and other elements sharply increase. Concentrations of principal cations reach high values because of their leaching from the crown by acid precipitation. The traditional concept of atmospheric load on boreal forests should be reconsidered taking into account their spatial structure.     

Soil- and plant-based countermeasures to reduce 137Cs and 90Sr uptake by grasses in natural meadows: the REDUP project.

The effectiveness of a set of soil- and plant-based countermeasures to reduce 137Cs and 90Sr transfer to plants was tested in natural meadows in the area affected by Chernobyl fallout. Countermeasures comprised the use of agricultural practices (disking + ploughing, liming and NPK fertilisation), addition of soil amendments and reseeding with a selection of grass species. Disking + ploughing was the most effective treatment, whereas the K fertiliser doses applied were insufficient to produce a significant increase in K concentration in soil solution. The application of some agricultural practices was economically justifiable for scenarios with a high initial transfer, such as 137Cs-contaminated organic soils. The use of soil amendments did not lead to a further decrease in transfer. Laboratory experiments demonstrated that this was because of their low radionuclide sorption properties. Finally, experiments examining the effect of plant species on radionuclide transfer showed that both transfer and biomass can depend on the plant species, indicating that those with high radionuclide root uptake should be avoided when reseeding after ploughing.     

240Pu/239Pu atom ratios in seawater from Sagami Bay, western Northwest Pacific Ocean: sources and scavenging

Seawater samples were collected in Sagami Bay, western Northwest Pacific Ocean, and their (239+240)Pu activities and (240)Pu/(239)Pu atom ratios were determined by alpha-spectrometry and sector field high-resolution ICP-MS. A few samples also were analyzed for (137)Cs activities. The (239+240)Pu inventory of 41.1 Bq m(-2) was equivalent to the expected cumulative deposition density of atmospheric global fallout at the same latitude and this inventory was considerably lower than inventories in the underlying sediment columns. This result indicated that a significant amount of (239+240)Pu has been removed into the underlying sediments through enhanced scavenging from the water column by the high fluxes of particles in this region. The atom ratio of (240)Pu/(239)Pu showed no notable variation from the surface to the bottom; the average value was 0.234+/-0.004. This atom ratio was significantly higher than the mean global fallout ratio of 0.18, proving the existence of close-in fallout plutonium originating from the Pacific Proving Grounds (PPG). The relative contributions of the global stratospheric fallout and the PPG close-in fallout were evaluated by using the two end-member mixing model. The contribution of the PPG close-in fallout was estimated to be 15.2 Bq m(-2), which corresponded to 37% of the (239+240)Pu inventory in the water column. Thus (239)Pu and (240)Pu from the two sources of global fallout and close-in fallout have been homogenized in the water masses in the western Northwest Pacific margin during the past three decades.     

Soil-water distribution coefficients and plant transfer factors for (134)Cs, (85)Sr and (65)Zn under field conditions in tropical Australia

Measurements of soil-to-plant transfer of (134)Cs, (85)Sr and (65)Zn from two tropical red earth soils ('Blain' and 'Tippera') to sorghum and mung crops have been undertaken in the north of Australia. The aim of the study was to identify factors that control bioaccumulation of these radionuclides in tropical regions, for which few previous data are available. Batch sorption experiments were conducted to determine the distribution coefficient (K(d)) of the selected radionuclides at pH values similar to natural pH values, which ranged from about 5.5 to 6.7. In addition, K(d) values were obtained at one pH unit above and below the soil-water equilibrium pH values to determine the effect of pH. The adsorption of Cs showed no pH dependence, but the K(d) values for the Tippera soils (2300-4100 ml/g) exceeded those for the Blain soils (800-1200 ml/g) at equilibrium pH. This was related to the greater clay content of the Tippera soil. Both Sr and Zn were more strongly adsorbed at higher pH values, but the K(d) values showed less dependence on the soil type. Strontium K(d)s were 30-60 ml/g whilst Zn ranged from 160 to 1630 ml/g for the two soils at equilibrium pH. With the possible exception of Sr, there was no evidence for downward movement of radionuclides through the soils during the course of the growing season. There was some evidence of surface movement of labelled soil particles. Soil-to-plant transfer factors varied slightly between the soils. The average results for sorghum were 0.1-0.3 g/g for Cs, 0.4-0.8 g/g for Sr and 18-26 g/g for Zn (dry weight) with the initial values relating to Blain and the following values to Tippera. Similar values were observed for the mung bean samples. The transfer factors for Cs and Sr were not substantially different from the typical values observed in temperate studies. However, Zn transfer factors for plants grown on both these tropical soils were greater than for soils in temperate climates (by more than an order of magnitude). This may be related to trace nutrient deficiency and/or the growth of fungal populations in these soils. The results indicate that transfer factors depend on climatic region together with soil type and chemistry and underline the value of specific bioaccumulation data for radionuclides in tropical soils.     

Uptake of radionuclides and stable elements from paddy soil to rice: a review

The critical paths for radionuclides and the critical foods in Asian countries differ from those in Western countries because agricultural products and diets are different. Consequently, safety assessments for Asian countries must consider rice as a critical food. As most rice is produced under flooded conditions, the uptake of radionuclides by rice is affected by soil conditions. In this report, we summarize radionuclide and stable element soil-to-plant transfer factors (TFs) for rice. Field observation results for fallout ¹³⁷Cs and stable Cs TFs indicated that while fallout ¹³⁷Cs had higher TF than stable Cs over several decades, the GM (geometric mean) values were similar with the GM of TF value for ¹³⁷Cs being 3.6 × 10⁻³ and that for stable Cs being 2.5 × 10⁻³. Although there are some limitations to the use of TF for stable elements under some circumstances, these values can be used to evaluate long-term transfer of long-lived radionuclides in the environment. The compiled data showed that TF values were higher in brown rice than in white rice because distribution patterns for elements were different in the bran and white parts of rice grains.     

Transfer of radiocobalt from soil to selected plant species in tropical environments

Soil-to-plant transfer factors (TFs) of radiocobalt (60Co) were determined in pot experiments for leafy vegetation, root crops and rice grown in the tropical environment of Bangladesh. Soil properties were also measured to establish a relationship between these properties and TF values. Measured TF values of 60Co for leafy vegetation (average of 2.2 x 10(-2)) were slightly higher than the values obtained for root vegetation (average of 1.6 x 10(-2)). However, TF values obtained for rice (average of 1.17 x 10(-2)) were about a factor of 2 lower than the values obtained for leafy vegetation. TF values of 60Co for leafy vegetation and root crops were observed to decrease with increasing pH, exchangeable K+ and clay content in the soil, even though poor correlations were estimated statistically. No consistent relationship between the TF value for 60Co and organic matter content could be deduced. The results presented here provide a useful addition to existing databases on soil-plant transfer for 60Co, since this information is still rather sparse for tropical environments.     

基于土壤侵蚀模型的滑波临界雨量估算探讨

针对滑坡临界雨量确定目前存在的问题,提出一种基于土壤侵蚀模型的滑坡临界雨量估算的新方法。该方法基本思路是：降雨引起土壤侵蚀,当土壤侵蚀达到一定强度时可诱发滑坡,因此利用土壤侵蚀模型可以推算滑坡临界雨量。以湖北省秭归县为例进行试验,从降雨-土壤侵蚀-滑坡的成灾机理入手,利用卫星资料、地理信息资料及降雨资料,计算降雨侵蚀力、土壤可蚀性、地形（坡长、坡度）、植被覆盖和土地利用类型等因子,基于USLE土壤侵蚀模型,计算滑坡发生时土壤侵蚀强度,通过分析多个滑坡个例,确定滑坡临界土壤侵蚀强度,再根据降雨侵蚀力与降雨量之间的关系,推算不同预警点滑坡临界雨量。相比以往仅仅分析灾情与降雨之间关系的传统方法,该方法有较为清晰的物理意义,实际业务中也易于实现,在滑坡预警预报中有较高实用价值     

Laboratory experiments to predict changes in radiocaesium root uptake after flooding events

Changes in soil solution composition after a flooding event were hypothesised to be one of the key factors in explaining changes in radiocaesium incorporation in the food chain in the areas affected by the Chernobyl accident. A laboratory methodology was set up to monitor changes in the soil solution composition after a sequence of flooding cycles. Experiments were performed using column and batch approaches on test soils with contrasting initial soil solution composition (high and low initial concentrations of K+). Results from column experiments indicated a potential increase in NH(4)(+) concentrations, a parameter which could lead to an increase in the radiocaesium root uptake. Batch results in the soil with high initial K+ concentration showed that after a number of flooding cycles, especially for high ratios of flooding solution/mass of soil, K+ concentration decreased sometimes below a threshold value (around 0.5-1 mmol l(-1)), a fact that could lead to an increase in radiocaesium transfer. For the soils with a low initial K+ concentration, the flooding solution increased K+ and NH(4)(+) values in the soil solution. The comparison of test soils with soils from Ukraine areas affected by flooding showed that the final stage in soil solution composition was similar in both cases, regardless of the initial composition of the soil solution. Moreover, the comparison with unflooded soils from the same area showed that potential changes in other soil parameters, such as (137)Cs activity concentration, clay content, and radiocaesium interception potential, RIP (a parameter that estimates the radiocaesium specific sorption capacity of a soil), should also be monitored for additional effects due to the flooding event. Therefore, the changes in the root uptake would depend on the resulting situation from changes in RIP, K+ and NH(4)(+) values in the soil solution.     

Precipitation scavenging of 7Be and 137Cs radionuclides in air

Atmospheric depositional fluxes of the naturally occurring 7Be of cosmogenic origin and 137Cs from fallout of the Chernobyl accident were measured over a 6-year period (January 1987-December 1992) at Thessaloniki, Greece (40 degrees 38'N, 22 degrees 58'E). Total precipitation accumulation during 1987-1992 varied between 33.7 cm and 65.2 cm, reflecting a relatively dry (precipitation-free) climate. The activity concentrations of 7Be and 137Cs in rainwater depended on the precipitation rate, being higher for low precipitation rates and lesser for high precipitation rates. 137Cs was removed by rain and snow more efficiently than 7Be. Snowfall was more efficient than rainfall in removing the radionuclides from the atmosphere. The annual bulk depositional fluxes of 7Be varied between 477 and 1133 Bq m(-2) y(-1) and this variability was attributed to the amount of precipitation and the variations of the atmospheric concentrations of 7Be. The annual bulk depositional fluxes of 137Cs showed a significant decrease over time from 1987 to 1992, resulting in a removal half-life of 1.33 years. The presence of 137Cs in air, and therefore in rainwater and snow, long after the Chernobyl accident (26 April 1986) was mainly due to the resuspension process. The normalized depositional fluxes of both radionuclides showed maximal values during the spring season where the maximum amount of precipitation occurred. The relatively high positive correlation between 7Be and 137Cs normalized depositional fluxes indicates that the scavenging process of local precipitation controlled the fluxes of both radionuclides. The dry depositional flux of 7Be was less than 9.37% of total (wet and dry) depositional flux. The fraction of dry-to-total depositional flux of 137Cs was much higher than that of 7Be, due to the resuspended soil.     

Exploring the fate,transport and risk of Perfluorooctane Sulfonate (PFOS) in a coastal region of China using a multimedia model

Perfluorooctane Sulfonate (PFOS) and related substances have been widely applied in both industrial processes and domestic products in China. Exploring the environmental fate and transport of PFOS using modeling methods provides an important link between emission and multimedia diffusion which forms a vital part in the human health risk assessment and chemical management for these substances. In this study, the gridded fugacity based BETR model was modified to make it more suitable to model transfer processes of PFOS in a coastal region, including changes to PFOS partition coefficients to reflect the influence of water salinity on its sorption behavior. The fate and transport of PFOS in the Bohai coastal region of China were simulated under steady state with the modified version of the model. Spatially distributed emissions of PFOS and related substances in 2010 were estimated and used in these simulations. Four different emission scenarios were investigated, in which a range of half-lives for PFOS related substances were considered. Concentrations of PFOS in air, vegetation, soil, fresh water, fresh water sediment and coastal water were derived from the model under the steady-state assumption. The median modeled PFOS concentrations in fresh water, fresh water sediment and soil were 7.20 ng/L, 0.39 ng/g and 0.21 ng/g, respectively, under Emission Scenario 2 (which assumed all PFOS related substances immediately degrade to PFOS) for the whole region, while the maximum concentrations were 47.10 ng/L, 4.98 ng/g and 2.49 ng/g, respectively. Measured concentration data for PFOS in the Bohai coastal region around the year of 2010 were collected from the literature. The reliability of the model results was evaluated by comparing the range of modeled concentrations with the measured data, which generally matched well for the main compartments. Fate and transfer fluxes were derived from the model based on the calculated inventory within the compartments, transfer fluxes between compartments and advection fluxes between sub-regions. It showed that soil and costal water were likely to be the most important sinks of PFOS in the Bohai costal region, in which more than 90% of PFOS was stored. Flows of fresh water were the driving force for spatial transport of PFOS in this region. Influences of the seasonal change of fresh water fluxes on the model results were also analyzed. When only seasonal changes of the fresh water flow rates were considered, concentrations of PFOS in winter and spring were predicted to be higher than that under annual average conditions, while the concentrations in summer and autumn were lower. For PFOS fluxes entering the sea, opposite conclusions were drawn compared to the concentrations. Environmental risks from the presence of PFOS in fresh water were assessed for this region through comparison with available water quality criteria values. The predicted concentrations of PFOS in the Bohai coastal region provided by the model were lower than the water quality criteria published by the United States Environmental Protection Agency and Chinese researchers, while the concentrations in more than 80% of the sampling locations exceeded the European Union Water Framework Directive Environmental Quality Standards values. Seasonal variations of flow rate might cause a significant increase in environmental risks.