Re-emission of heavy water vapour from soil to the atmosphere

The re-emission process of tritiated water (HTO) deposited on a soil surface is an important process to assess tritium doses to the general public around nuclear fusion facilities in future. A field experiment using heavy water (HDO) as a substitute for HTO was carried out in the summertime to investigate the re-emission process of HTO from soil to the atmosphere. In the experiment, the time variations of depth profiles of HDO concentrations in soil exposed to HDO vapour and soil mixed with HDO were measured during the re-emission process on the field. The HDO concentrations in soil water in top soil layers of both the exposed and mixed soil rapidly decreased with time during the re-emission. However, the decrease of exposed soil was much greater than that of mixed soil. The re-emission process was analysed using a model including the evaporation of HDO from soil, the exchange between soil HDO and air H2O, and the diffusion of HDO in soil. It was found that the model is applicable to calculating the time variations of detailed depth profiles of HDO concentration in soil water in surface soil layers, using an estimated exchange velocity.     

Assessment, validation and intercomparison of operational models for predicting tritium migration from routine discharges of nuclear power plants: the case of Loire River

During last decades, a number of projects have been launched to validate models for predicting the behaviour of radioactive substances in the environment. The project of the "Aquatic" working group of the project EMRAS (Environmental Modelling for Radiation Safety) organised by the International Atomic Energy Agency (IAEA) was based on the validation and assessment of models for predicting the behaviour of radionuclides in the aquatic ecosystems. The present paper describes a blind test of models aimed at assessing the dispersion of tritium releases in the Loire River (France), on a large domain ( approximately 350km) and on a period of six months, by comparing the results obtained by operational-to-experimental values of tritium concentration at Angers, a city along the Loire River. The common conclusion is that the models used by the different participants namely 1D models and models based on a schematic hydraulic (box models) are reliable tools for tritium transport modelling. Nevertheless, the importance of proper and detailed hydrological data for the appropriate prediction of pollutant migration in water is demonstrated by the example provided during this study.     

Development and validation of a dynamical atmosphere-vegetation-soil HTO transport and OBT formation model

A numerical model simulating transport of tritiated water (HTO) in atmosphere-soil-vegetation system, and, accumulation of organically bound tritium (OBT) in vegetative leaves was developed. Characteristic of the model is, for calculating tritium transport, it incorporates a dynamical atmosphere-soil-vegetation model (SOLVEG-II) that calculates transport of heat and water, and, exchange of CO₂. The processes included for calculating tissue free water tritium (TFWT) in leaves are HTO exchange between canopy air and leaf cellular water, root uptake of aqueous HTO in soil, photosynthetic assimilation of TFWT into OBT, and, TFWT formation from OBT through respiration. Tritium fluxes at the last two processes are input to a carbohydrate compartment model in leaves that calculates OBT translocation from leaves and allocation in them, by using photosynthesis and respiration rate in leaves. The developed model was then validated through a simulation of an existing experiment of acute exposure of grape plants to atmospheric HTO. Calculated TFWT concentration in leaves increased soon after the start of HTO exposure, reaching to equilibrium with the atmospheric HTO within a few hours, and then rapidly decreased after the end of the exposure. Calculated non-exchangeable OBT amount in leaves linearly increased during the exposure, and after the exposure, rapidly decreased in daytime, and, moderately nighttime. These variations in the calculated TFWT concentrations and OBT amounts, each mainly controlled by HTO exchange between canopy air and leaf cellular water and by carbohydrates translocation from leaves, fairly agreed with the observations within average errors of a factor of two.     

HTO and OBT activity concentrations in soil at the historical atmospheric HT release site (Chalk River Laboratories)

Tritium is routinely released by the Chalk River Laboratories (CRL) nuclear facilities. Three International HT release experiments have been conducted at the CRL site in the past. The site has not been disturbed since the last historical atmospheric testing in 1994 and presents an opportunity to assess the retention of tritium in soil. This study is devoted to the measurement of HTO and OBT activity concentration profiles in the subsurface 25 cm of soil.In terms of soil HTO, there is no evidence from the past HT release experiments that HTO was retained. The HTO activity concentration in the soil pore water appears similar to concentrations found in background areas in Ontario. In contrast, OBT activity concentrations in soil at the same site were significantly higher than HTO activity concentrations in soil. Elevated OBT appears to reside in the top layer of the soil (0-5 cm). In addition, OBT activity concentrations in the top soil layer did not fluctuate much with season, again, quite in contrast with soil HTO. This result suggests that OBT activity concentrations retained the signature of the historical tritium releases.     

Tritium profiles in snowpacks

The release of tritiated water (HTO) to the atmosphere during the winter can contribute significantly to snow contamination and to water-soil-plant contamination after the spring thaw. The dose significance of such a release depends on the persistence of tritiated water in the snowpack, which is primarily controlled by the HTO diffusion process in snow and the rate of re-emission into the atmosphere from the snowpack surface. Monitoring data collected after an acute winter release at Chalk River Laboratories and data obtained in winter over a chronically contaminated area were analyzed to estimate the diffusion coefficient of HTO in the snowpack. Under conditions of cold and dry snow, the diffusion coefficient lay in the range 1-2 × 10⁻¹⁰ m² s⁻¹, an order of magnitude lower than diffusion in water but an order of magnitude higher than self-diffusion in ice. These results confirm the theoretical predictions (Bales, 1991). Values up to six times higher were found for warmer periods and just before spring melt, when other processes contribute to profile evolution. The low diffusion rate of tritium in cold, dry snow means that tritium remains in the snowpack throughout the winter, to be released during spring thaw to potentially contaminate surface water, soil and crops.     

Time-series sampling of Ra and Ra at the inlet to Great South Bay (New York): a strategy for characterizing the dominant terms in the Ra budget of the bay

Ra isotopes are a powerful tool for quantifying the flux of submarine groundwater discharge (SGD) into the sea. Previous studies of ²²³Ra and ²²⁴Ra mass balances in coastal embayments have shown that the Ra balance is dominated by supply via SGD, exchange with the open ocean and radioactive decay. The current study shows that a single time series over a tidal cycle at the principal inlet to Great South Bay (NY, US) is sufficient to determine the net flux of Ra across the inlet, and also can be used to estimate the decay of short-lived Ra in the bay. Estimates of the net Ra flux obtained from a single tidal time-series by using three different approaches agree with those determined from a more time-consuming survey of Ra within the bay, and may represent a first step of estimating SGD in bays and coastal lagoons.     

The effect of tropopause height on the content of radioactive debris in surface atmosphere

The effect of tropopause height on the content of ¹³⁷Cs and total beta activity in surface atmosphere was considered for the period of intensive nuclear weapon tests, from 1968–1971. The activity of ¹³⁷Cs in monthly air filter samples was measured by gamma spectrometry and total beta activity was determined by 2π proportional counters. The results were correlated with data on tropopause height. The results indicate that the movement of radioactive debris from the stratosphere into the troposphere occurs simultaneously with the changes in tropopause height. The content of long lived radionuclides in the troposphere follows the changes with a certain delay due to meteorological conditions in surface air and due to the location of sampling.     

Radioecological consequences of radioactive discharges into the Techa River on the Southern Urals

The sources and levels of radioactive contamination of the Techa River are analyzed. Dose assessments are made for humams and biota. The highest radionuclide concentrations in the river water were observed in the period 1950–1951. In 1951, at a distance of 78 km from the site of radioactive discharges, the content of ⁹⁰Sr in the water was 2.7 × 10⁴ Bq l⁻¹ and that of ¹³⁷Cs was 7.5 × 10³ Bq l⁻¹. Subsequently, the radionuclide activity in the river water decreased considerably. In the period 1991–1994, the average annual content of ⁹⁰Sr in the water varied between 6 and 20 Bq l⁻¹. The average annual content of ¹³⁷Cs in the river water varied from 0.06 to 0.23 Bq l⁻¹, i.e. was lower than that of ⁹⁰Sr approximately by two orders of magnitude. The concentration of ^239,240Pu in the water varied between 0.004 and 0.019 Bq l⁻¹. The radioactive contamination of the Techa floodplain is highly nonuniform. With increasing distance from the river sources, the contamination density of the floodplain decreases, remaining, however, considerably higher than the background values.At present, the average annual dose rates in contaminated areas are (0.1–2) × 10⁻³ Sv year⁻¹, which is considerably lower than in the periods of ‘acute’ exposure (1950–1951). The doses to aquatic biota were much higher than those to humans.     

The relationship of climatic and hydrological parameters to surface water quality in the lower Mekong River

The relationship between climatic, hydrological and water quality parameters of the lower Mekong River flowing through four different countries (Thailand, Cambodia, Lao PDR and Vietnam) was studied. The Mekong River Commission (MRC) secondary data of climatic and hydrological parameters included precipitation, evaporation, average air temperatures, mean water level and discharge flow. Water quality parameters consisted of TSS, NO(3)(-), PO(4)(3-), DO, pH, conductivity, Ca, Mg, Na, K, alkalinity, Cl, SO(4)(2-), Fe, TP, Si and COD. Pearson's correlation was used to determine their relationship. The results reveal that the correlations of climatic, hydrological and water quality parameters in those four countries located along the lower Mekong River had the same trend. Precipitation had fair positive correlations with mean water level (ranging 0.375-0.661), discharge flow (ranging 0.526-0.659) and mean air temperature (ranging 0.515-0.621), however had weak negative correlation with evaporation (ranging 0.169-0.468). Concerning relationship with water quality, the results show that TSS, NO(3)(-), PO(4)(3-), TP and COD had weak to fair positive correlations with precipitation, mean water level, discharge flow. However, DO, pH, conductivity, Ca, Mg, Na, K, alkalinity, Cl, SO(4)(2-) and Si had fair to strong negative correlations with all hydrological parameters. Finally, TSS, alkalinity and conductivity were proposed as sensitive water quality parameters for monitoring impacts of changing climate in the lower Mekong River.     

Preliminary assessment of current radiation doses to the population of Brodokalmak from contamination of the Techa River

Significant quantities of liquid radioactive waste were discharged to the Techa River in the southern Urals region of Russia in the early years of operation of the Mayak PA plant (1948–1951). A collaborative project is underway under contract to the European Commission to consider the radiological impact of radioactive contamination in the Southern Urals. Part of this project involves the calculation of radiation doses currently received by the population of Brodokalmak on the Techa river. The assessment made use of local data on the habits of the population and measurements of radionuclide activity concentrations in food and water. Exposure pathways included in the assessment were ingestion of foods and external exposure to gamma radiation from radionuclides deposited on the banks of the river. A range of doses was calculated for different age groups, firstly, assuming that the restrictions in place are retained and, secondly, assuming that there are no restrictions. These restrictions include bans on drinking river water, fishing and bathing in the river and the prohibition of use of the river and surrounding flood plains by humans and cattle. With restrictions the highest dose estimated was 0.56 mSv y⁻¹ for the most exposed adults and without restrictions this increased to 3.4 mSv y⁻¹.     

贵州阿哈湖喀斯特小流域DOC输出特征

河流不仅是陆地碳循环的通道,也是碳交换的重要场所,而小流域更被认为是陆地碳循环的热点。为探究人类活动影响下喀斯特小流域溶解性有机碳(DOC)输出特征,于2017年6月～2018年5月对阿哈湖3条主要入湖小流域游鱼河、白岩河、金钟河河水主要理化特征和DOC含量进行分析,并计算流域DOC输出通量。研究期间游鱼河、白岩河、金钟河DOC含量分别为4.78±2.11、5.61±2.27、7.40±2.51 mg/L,输出通量分别为2.71、2.91、3.82 t/(km~2. a)。结果表明:(1)阿哈湖小流域河水DOC含量时空变化特征明显,与降雨、流域土地利用类型密切相关,人类外源输入对DOC有显著影响;(2)对比不同河流DOC输出特征发现,小流域通常具有更高的DOC输出通量,特别是受城市输出影响的中小流域,其河流碳过程在碳循环中的贡献可能被低估。     

Fukushima fallout in Northwest German environmental media

Traces of short- and long-lived fallout isotopes (¹³¹I, ¹³⁴Cs and ¹³⁷Cs) were found in environmental samples collected in Northwest Germany (rain water, river sediment, soil, grass and cow milk) from March to May 2011, following the radioactivity releases after the nuclear accident in Fukushima, Japan. The measured concentrations are consistent with reported concentrations in air, amount of rainfall and expected values applying simple radioecological models. The [¹³⁴Cs]/[¹³⁷Cs] ratio reported for air (about 1) allows for discrimination between “recent” and “old” ¹³⁷Cs. Expected ¹³⁶Cs values fell below the detection limits of the instrumentation, despite large sample masses and long counting times.     

Sedimentary radioactive tracers and diffusive models

This paper examines the underlying assumptions and consequences of applying a steady-state equation to sediment profiles of radioactive tracers in order to deconvolute sedimentation from bioturbation processes modelled as a diffusive type process.Several factors follow immediately from this investigation:

(i)

if the observed radioactive concentration increases with depth over any finite depth range then the proposed steady-state, constant flux equation is not applicable. Any increase in radioactive concentration with depth implies a negative mixing coefficient which is a physical impossibility;

(ii)

when the radioactive concentration systematically decreases with increasing sedimentary depth then solutions to the steady-state conservation equation exist only when either the constant solid state flux to the sediment surface is small enough so that a positive mixing coefficient results or when the mixing coefficient is small enough so that a positive flux results.

If the radioactive concentration, porosity and/or density of the solid phase are such that the proposed equation is inappropriate (because no physically acceptable solution exists) then one must abandon the proposed steady-state equation.Further: if the flux of solid sediment to the sediment surface varies with time then, of course, a steady-state conservation equation is also inappropriate.Simple examples illustrate that the assumption of steady-state restricts the applicability of this modelling approach to a relatively small sub-set of expected situations in the real world.     

流域气候变化和人类活动对长江径流量影响的辨识

利用1956~2011年的流域气温、降水量、径流量及有关文献所载蒸发量、水库修建、用水量、水土保持等资料，探讨气候变化和人类活动对长江径流量的影响。结果表明：（1）流域气温明显上升，且上升速率大于全球平均上升速率;（2）流域平均降水量下降了约1%，年降水量与年均气温之间无显著相关性;（3）年径流量随降水量频繁振荡，最大和最小值之比达19;（4）太阳净辐射量和风速下降导致流域自然蒸发作用减弱，而水库修建、耗水增多和水土保持等人类活动则使蒸发作用加强。两方面的影响相互削弱；入海年径流量下降1%;（5）流域内分区间存在差异，北域（岷江、嘉陵江和汉江）人类活动的影响居主导地位，径流量下降约15%；中域（金沙江以下干流两翼“未测区”）则以气候变化的影响占优，径流量上升约9%；西域（金沙江流域）径流量减少4%；南域（乌江、洞庭湖和鄱阳湖流域）径流量上升2%。推断今后几十年气候要素仍将主导径流量的年际波动，而南水北调、新建水库、耗水增多和水土保持加强将可能使径流量再下降约10%     

流域过境水对流域水循环的影响——以太湖流域地表水平衡为例

流域水循环是流域生态系统的核心,其中流域过境水是流域水循环的一个重要要素。通过对大量有关太湖流域水文资料的流域水平衡分析,初步探讨太湖流域过境水对流域水循环的影响。结果显示太湖流域是长江流域中受过境水强烈影响的一个子流域。在太湖流域,流域过境水的引入扩大了流域水循环总的通量,影响了流域水循环的路径,改变了流域水循环水的配置格局。同时水循环作为流域内物质运输的介质,流域过境水的引入对太湖流域内物质的运输有不可忽视的影响,其中最重要的就是影响了污染物的运输,增加了污染物在太湖当中的沉积与滞留     

A review and model assessment of (32)P and (33)P uptake to biota in freshwater systems

Bioaccumulation of key short-lived radionuclides such as ¹³¹I and ^32,33P may be over-estimated since concentration ratios (CRs) are often based on values for the corresponding stable isotope which do not account for radioactive decay during uptake via the food chain. This study presents estimates for bioaccumulation of radioactive phosphorus which account for both radioactive decay and varying ambient levels of stable P in the environment. Recommended interim CR values for radioactive forms of P as a function of bioavailable stable phosphorus in the water body are presented. Values of CR are presented for three different trophic levels of the aquatic food chain; foodstuffs from all three trophic levels may potentially be consumed by humans. It is concluded that current recommended values of the CR are likely to be significantly over-estimated for radioactive phosphorus in many freshwater systems, particularly lowland rivers. Further research is recommended to field-validate these models and assess their uncertainty. The relative importance of food-chain uptake and direct uptake from water are also assessed from a review of the literature. It can be concluded that food-chain uptake is the dominant accumulation pathway in fish and hence accumulation factors for radioactive phosphorus in farmed fish are likely to be significantly lower than those for wild fish.     

Emission factors for PCDD/PCDF and dl-PCB from open burning of biomass

The Stockholm Convention on Persistent Organic Pollutants includes in its aims the minimisation of unintentional releases of polychlorinated dibenzo-dioxins and dibenzofurans (PCDD/PCDF) and dioxin like PCB (dl-PCB) to the environment. Development and implementation of policies to achieve this aim require accurate national inventories of releases of PCDD/PCDF/dl-PCB. To support this objective, the Conference of Parties established a process to review and update the UNEP Standardized Toolkit for Identification and Quantification of Dioxin and Furan Releases. An assessment of all emission inventories was that for many countries open burning of biomass and waste was identified as the major source of PCDD/PCDF releases. However, the experimental data underpinning the release estimates used were limited in number and, consequently, confidence in the accuracy of the emissions predictions was low. There has been significant progress in measurement technology since the last edition of the Toolkit in 2005. In this paper we reassess published emission factors for release of PCDD/PCDF and dl-PCB to land and air.In total, four types of biomass and 111 emission factors were assessed. It was found that there are no systematic differences in emission factors apparent between biomass types or fire classes. The data set is best described by a lognormal distribution. The geometric mean emission factors (EFs) for releases of PCDD/PCDF to air for the four biomass classes used in the Toolkit (sugarcane, cereal crops, forest and savannah/grass) are 1.6 μg TEQ (t fuel)⁻¹, 0.49 μg TEQ (t fuel)⁻¹, 1.0 μg TEQ (t fuel)⁻¹ and 0.4 μg TEQ (t fuel)⁻¹, respectively. Corresponding EFs for release of PCDD/PCDF to land are 3.0 ng TEQ (kg ash)⁻¹, 1.1 ng TEQ (kg ash)⁻¹, 1.1 ng TEQ (kg ash)⁻¹ and 0.67 ng TEQ (kg ash)⁻¹. There are now also sufficient published data available to evaluate EFs for dl-PCB release to air for sugarcane, forest and grass/savannah; these are 0.03 μg TEQ (t fuel)⁻¹, 0.09 μg TEQ (t fuel)⁻¹ and 0.01 μg TEQ (t fuel)⁻¹, respectively. The average EF for dl-PCB release to land is 0.19 ng TEQ (kg ash)⁻¹. Application of these EFs to national emissions of PCDD/PCDF for global estimates from open burning will lower previous estimates of PCDD/PCDF releases to air and to land by 85% and 90%, respectively. For some countries, the ranking of their major sources will be changed and open burning of biomass will become less significant than previously concluded.     

Water to atmosphere fluxes of 131I in relation with alkyl-iodide compounds from the Seine Estuary (France)

This study presents an original work on measurements of stable and radioactive iodinated species in the Seine estuary (France), with estimates fluxes of volatile gaseous species from water to the atmosphere. Various iodinated compounds were identified in water and air in particular 131I in water, what is unusual. Concentrations and behaviour of iodinated elements in the Seine estuary seem similar to what has been observed in other European estuaries. MeI (Methyl Iodide) and Total Volatile Iodine (TVI) fluxes from water to air vary between 392 and 13949 pmol m(-2) d(-1) and between 1279 and 16484 pmol m(-2) d(-1), respectively. Water to air flux of TVI for the Seine river was estimated in the range 4-46 kg y(-1). Measurements of (131)I in water varying between 0.4 and 11.9 Bq m(-3). Fluxes of (131)I from water to atmosphere are in the range 2.4 x 10(5)-1.3 x 10(7)Bq y(-1), close to an annual discharge of (131)I by a nuclear reactor.     

Possible health effects of energy conservation: Impairment of indoor air quality due to reduction of ventilation rate

Efforts to reduce the energy needs to heat or cool dwellings have the potential to create new health hazards. Increases in indoor levels of radon and its progeny from the reduction in air exchange rates add a substantial radioactive burden to the general population. Other indoor pollutants reaching critical concentrations in homes with low air exchange rates are CO and NO₂ from unvented combustion in gas stoves and heaters, tobacco smoke, and asbestos fibers. In addition, insulation materials and certain types of furniture may contribute the toxicant formaldehyde diffusing from foam injected walls or chipboard. Risk estimations using linear dose-response relationships show risk factors per kWh saved which are orders of magnitude greater than for a kWh produced by large power plants using coal, oil, gas, or uranium.     

Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH₃T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH₃T concentrations. The HT and CH₃T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH₃T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH₄ to estimate global warming in its 2007 report. The longer environmental half-life of CH₃T suggested its supply from other sources than past nuclear weapon testing in the atmosphere.