Mobilization of aluminium and deposition on fish gills during sea salt episodes--catchment liming as countermeasure

Episodic events may be critical with respect to aluminium (Al) toxicity in moderately acidified salmon rivers. The present work demonstrates that sea salt episodes enhance the toxicity of Al in acidic rivers. The documented sea salt episode (300 [micro sign]M Cl) mobilized positively charged Al species (0.4 to 1.1 [micro sign]M Al(i)), enhanced the Al accumulation on fish gills (0.9 to 10 [micro sign]mol g(-1) dw) and caused increased stress responses (6 to15 mM blood glucose) in fish. Accumulated Al on gills remained high several days after the episode. The presented results are based on a six-week field study in two tributary rivers on the west coast of Norway. Changes in the river water qualities and Al speciation were followed using in situ fractionation techniques. Al accumulation on gills and stress responses were followed for Atlantic salmon (Salmo salar) kept in tanks continually exposed to the changing water quality. The potential mobilization of Al from the two catchments was studied by extracting soils with diluted seawater (salinity of 3). To counteract Al toxicity, one of the tributary catchments has been limed. The potential mobility of Al by sea salt was lower in limed soils compared to acid soils, and the Al deposition on fish gills (<3.5 [micro sign]mol g(-1) dw) and associated stress responses stayed low during the sea salt episode in the river draining the limed catchment. Thus, for acid river systems in coastal areas, catchment liming should be considered as a useful countermeasure for Al toxicity.     

Vertical distribution of anthropogenic radionuclides in cores from contaminated floodplains of the Yenisey River

The Mining and Chemical Industrial Combine, Zheleznogorsk (MCIC, previously known as Krasnoyarsk-26) on the River Yenisey has contaminated the surrounding environment with anthropogenic radionuclides as a result of discharges of radioactive wastes. The purpose of this study was to investigate the vertical distribution of anthropogenic contamination (¹³⁷Cs and plutonium) within floodplain areas at different distances from the discharge point. Sites were chosen that display different characteristics with respect to periodic inundation with river water. Cs-137 activity concentrations were in the range 23–3770 Bq/kg (dry weight, d.w.); Pu-239,240 activity concentrations were in the range <0.01–14.2 Bq/kg (d.w.). Numerous sample cores exhibited sub-surface maxima which may be related to the historical discharges from the MCIC. Possible evidence indicating the deposition of earlier discharges at MCIC in deeper core layers was observed in the ²³⁸Pu:^239,240Pu activity ratio data: a Pu signal discernible from global fallout could be observed in numerous samples. Cs-137 and Pu-239,240 activity concentrations were correlated with the silt fraction (% by mass <63 μm) though no significant correlation was observed between (grain-size) normalised ¹³⁷Cs activity concentrations and distance downstream from the MCIC.     

Radionuclide contamination of sediment deposits in the Ob and Yenisey estuaries and areas of the Kara Sea

The Ob and Yenisey rivers are major contributors to total riverine discharge to the Arctic Ocean. Several large nuclear facilities discharge into these rivers, which could affect actual and potential discharges of radionuclides to the Arctic region. This article presents new radionuclide concentration and grain-size data resulting from analyses of several sediment samples collected during research cruises in the Ob and Yenisey estuaries and adjacent areas during 2000 and 2001. Results indicate that discharges from the main nuclear facilities do not constitute a major contribution to the level of radioactive contamination in the marine areas studied, though Co-60 was detected at low concentrations in some sediment horizons. However, the aggregate contamination from different sources is not radioecologically significant in sediments within the study area, maximum Cs-137 levels being approximately 80 Bq kg(-1) dry weight.     

On-site gamma dose rates at the Andreeva Bay shore technical base, northwest Russia

The spent nuclear fuel (SNF) and radioactive waste (RAW) storage facility at Andreeva Bay shore technical base (STB) is one of the largest and most hazardous nuclear legacy sites in northwest Russia. Originally commissioned in the 1960s the facility now stores large amounts of SNF and RAW associated with the Russian Northern Fleet of nuclear powered submarines. The objective of the present study was to map ambient gamma dose rates throughout the facility, in particular at a number of specific sites where SNF and RAW are stored. The data presented here are taken from a Norwegian-Russian collaboration enabling the first publication in the scientific literature of the complete survey of on-site dose rates. Results indicate that elevated gamma dose rates are found primarily at discrete sites within the facility; maximum dose rates of up to 1000 microSv/h close to the ground (0.1m) and up to 3000 microSv/h at 1m above ground were recorded, higher doses at the 1m height being indicative primarily of the presence of contaminated equipment as opposed to ground contamination. Highest dose rates were measured at sites located in the immediate vicinity of buildings used for storing SNF and sites associated with storage of solid and liquid radioactive wastes. Elevated dose rates were also observed near the former channel of a small brook that became heavily contaminated as a result of radioactive leaks from the SNF storage at Building 5 starting in 1982. Isolated patches of elevated dose rates were also observed throughout the STB. A second paper detailing the radioactive soil contamination at the site is published in this issue of Journal of Environmental Radioactivity.     

Remobilisation of 109Cd, 65Zn and 54Mn from freshwater-labelled river sediments when mixed with seawater

A major fraction of trace metals transported by rivers is associated with sediments, especially during flooding, when erosion and resuspension increase sediment loads. Upon contact with seawater in estuaries, changes in ionic strength and pH may remobilise trace metals from sediment surfaces into more bioavailable forms. The objective of the present work was to investigate time-dependent interactions between trace metals and freshwater sediments and their potential remobilisation upon contact with seawater. Two river sediments (one organic and one inorganic) were labelled with 109Cd2+, 65Zn2+ and 54Mn2+ radioactive tracers for periods up to 6 months. Sorption of tracers occurred rapidly (> or = 80% sorption, < 1 h), followed by a slower approach to pseudoequilibrium. Kd(6 months) were estimated as 460, 480 and 2200 ml/g (inorganic sediment) compared to 5300, 4000 and 1200 ml/g (organic sediment) for 109Cd, 65Zn and 54Mn, respectively. Remobilisation of tracers from labelled sediments was studied using sequential extractions. Artificial seawater extracts simulated an estuarine environment. Subsequent extractions provided information about more strongly sorbed tracer fractions within sediments. Remobilisation of 109Cd by seawater was significant (> 65%) and least affected by sediment type or freshwater labelling time. Redistribution of Cd to strongly bound phases was minimal (4% and 1% of 109Cd in strongly oxidisable fractions). Seawater remobilisation of 65Zn was significantly greater from the organic sediment (54%) compared to the inorganic sediment (8%), where a large fraction of 65Zn (14%) became irreversibly bound. Similarly, more 54Mn was remobilised by seawater from the organic sediment than the inorganic sediment (66% and 3% remobilised, respectively), i.e., 54Mn became more strongly bound in the inorganic sediment. A simple three-box model, based on first-order differential equations, was used to describe the interaction between tracers in spiked freshwater and two operationally defined sediment fractions ("seawater exchangeable" and "seawater unexchangeable") up to 6 months of freshwater labelling. Model simulations were fitted to experiment data and apparent rate constants were calculated using numerical optimisation methods. Sorption ratios from modelling data (i.e., k1/k2) were greater for organic compared to inorganic sediments, while fixation ratios were higher in inorganic sediments. In conclusion, trace metals can be remobilised from sediments on contact with seawater in estuaries. High organic content in sediments increased initial sorption of tracers but inhibited redistribution to more strongly bound fractions over time, resulting in greater remobilisation of tracers when in contact with seawater.     

Norway's role in international collaboration towards rehabilitation of Andreeva Bay

Andreeva Bay is one of the largest and most hazardous nuclear legacy sites in northwest Russia. The site is the location of large amounts of Spent Nuclear Fuel (SNF) and radioactive wastes and the risks associated with the site have precipitated an extensive international collaborative effort towards securing and rehabilitating the site. Given the location and proximity of the site, Norway has and continues to contribute in a number of ways towards this effort. Norway's activities in relation to rehabilitative efforts at Andreeva Bay are focused on both infrastructural and remediative initiatives as well as regulatory collaboration with Russia towards ensuring effective and safe operations during handling and removal of SNF and radioactive materials. This article describes Norway's role within international efforts in the context of the rehabilitation of Andreeva Bay and outlines previous activities and Norway's future direction with respect to the site.     

Application of an environmental impact assessment methodology to a site discharging low levels of radioactivity to a freshwater environment in Norway

Significant shifts in opinion regarding environmental protection from ionising radiation have resulted in the development and availability of bespoke approaches for the assessment of impacts on wildlife from radioactive contaminants. The application of such assessment methodologies to actual situations, however, remains relatively limited. This paper describes the implementation of the ERICA Integrated Approach and associated tools within the context of routine discharges of radioactive materials to a freshwater environment. The article follows the implementation through its relevant stages and discusses strengths and weaknesses of the approach in relation to the case study. For current discharge levels, ¹³⁷Cs and ⁶⁰Co constitute the main dose contributors to the majority of reference organisms studied, although ²⁴¹Am and ³H are the main contributors for the phyto- and zooplankton categories. Patterns are observed depending on whether the reference organism is sediment-associated or not. At current discharge levels, none of the reference organisms exceeded or approached the selected screening level, and impacts on biota could be regarded as negligible.     

A Strategy for the Evaluation of Sensory and Pulmonary Irritation Due to Chemical Emissions from Indoor Sources

Abstract

Sensory and pulmonary irritation are physiological responses to chemical exposure which result in characteristic, measurable changes in respiratory activity in mice. A standard method has been applied to the estimation of sensory irritation associated with a specific chemical exposure. This method has been correlated with human responses to these chemicals. Symptoms associated with chemical irritants are consistent with complaints due to problems with indoor air quality, which may include eye and upper respiratory tract irritation, headaches, and nausea. A stepwise strategy for assessing the contribution of indoor products to sensory and pulmonary irritation is discussed in the current paper. The strategy includes product emissions testing using dynamic environmental chambers, the selection of suspected irritants for respiratory irritation testing, respiratory irritation testing of individual compounds and representative mixtures using synthesized atmospheres, and the evaluation of test data to determine those compounds which may contribute to sensory and pulmonary irritation in humans. The current strategy is being applied to evaluate carpet system materials and their constituent chemicals.     

On-site radioactive soil contamination at the Andreeva Bay shore technical base, Northwest Russia

The radioactive waste (RAW) storage site at Andreeva Bay in the Russian Northwest has experienced radioactive contamination both as a result of activities carried out at the site and due to incidents that have occurred there in the past such as accidental releases of radioactive materials. The site is an interesting case study for decommissioning due to the extremely large amounts of radioactivity present at the site and the conditions under which it is stored; very little has been previously published in the scientific literature about this site. This paper complements the paper describing dose rates at Andreeva Bay which is published in this issue of Journal of Environmental Radioactivity by the same authors. This study presents new data related to the activity concentrations of (137)Cs and (90)Sr in surface soils and measurements of alpha- and beta-particle fluxes taken at different areas around the site. Limited data on 60Co is also presented. The results of the study indicate that the main areas of site contamination are associated with the former spent nuclear fuel storage facility at Building 5, due to accidental discharges which began in 1982. Substantial contamination is also observed at the solid radioactive waste storage facilities, probably due to the ingress of water into these facilities. More than 240 samples were measured: maximum contamination levels were 1 x 10(6)Bq/kg (137)Cs (mean value 4.1 x 10(5)Bq/kg) and 4 x 10(6)Bq/kg (90)Sr (mean value 1.2 x1 0(5)Bq/kg). Localised patches of alpha and beta contamination were also observed throughout the site.     

Will global warming affect soil-to-plant transfer of radionuclides?

Recent assessments of global climate/environmental change are reaching a consensus that global climate change is occurring but there is significant uncertainty over the likely magnitude of this change and its impacts. There is little doubt that all aspects of the natural environment will be impacted to some degree. Soil-to-plant transfer of radionuclides has long been a significant topic in radioecology, both for the protection of humans and the environment from the effects of ionising radiation. Even after five decades of research considerable uncertainty exists as to the interplay of key environmental processes in controlling soil-plant transfer. As many of these processes are, to a lesser or greater extent, climate-dependent, it can be argued that climate/environmental change will impact soil-to-plant transfer of radionuclides and subsequent transfers in specific environments. This discussion attempts to highlight the possible role of climatic and climate-dependent variables in soil-to-plant transfer processes within the overall predictions of climate/environmental change. The work is speculative, and intended to stimulate debate on a theme that radioecology has either ignored or avoided in recent years.