Journal of Environmental Radioactivity

Publisher: Elsevier

Current impact factor: 2.48

Impact Factor Rankings

2016 Impact Factor Available summer 2017
2014 / 2015 Impact Factor 2.483
2013 Impact Factor 3.571
2012 Impact Factor 2.119
2011 Impact Factor 1.339
2010 Impact Factor 1.466
2009 Impact Factor 1.268
2008 Impact Factor 1.114
2007 Impact Factor 0.963
2006 Impact Factor 1.073
2005 Impact Factor 1.243
2004 Impact Factor 1.188
2003 Impact Factor 0.837
2002 Impact Factor 0.674
2001 Impact Factor 0.726
2000 Impact Factor 0.764
1999 Impact Factor 0.881
1998 Impact Factor 0.958
1997 Impact Factor 0.638
1996 Impact Factor 1.014
1995 Impact Factor 0.672
1994 Impact Factor 0.505
1993 Impact Factor 0.484
1992 Impact Factor 0.436

Impact factor over time

Impact factor

Additional details

5-year impact 2.32
Cited half-life 6.90
Immediacy index 0.31
Eigenfactor 0.01
Article influence 0.56
ISSN 1879-1700

Publisher details


  • Pre-print
    • Author can archive a pre-print version
  • Post-print
    • Author can archive a post-print version
  • Conditions
    • Authors pre-print on any website, including arXiv and RePEC
    • Author's post-print on author's personal website immediately
    • Author's post-print on open access repository after an embargo period of between 12 months and 48 months
    • Permitted deposit due to Funding Body, Institutional and Governmental policy or mandate, may be required to comply with embargo periods of 12 months to 48 months
    • Author's post-print may be used to update arXiv and RepEC
    • Publisher's version/PDF cannot be used
    • Must link to publisher version with DOI
    • Author's post-print must be released with a Creative Commons Attribution Non-Commercial No Derivatives License
    • Publisher last reviewed on 03/06/2015
  • Classification

Publications in this journal

  • [Show abstract] [Hide abstract]
    ABSTRACT: Iodine-129 has been used as a powerful tool for environmental tracing of human nuclear activities. In this work, a sediment core collected from Jiaozhou Bay, the east coast of China, in 2002 was analyzed for 129I to investigate the influence of human nuclear activities in this region. Significantly enhanced 129I level was observed in upper 70 cm of the sediment core, with peak values in the layer corresponding to 1957, 1964, 1974, 1986, and after 1990. The sources of 129I and corresponding transport processes in this region are discussed, including nuclear weapons testing at the Pacific Proving Grounds, global fallout from a large numbers of nuclear weapon tests in 1963, the climax of Chinese nuclear weapons testing in the early 1970s, the Chernobyl accident in 1986, and long-distance dispersion of European reprocessing derived 129I. The very well 129I records of different human nuclear activities in the sediment core illustrate the potential application of 129I in constraining ages and sedimentation rates of the recent sediment. The releases of 129I from the European nuclear fuel reprocessing plants at La Hague (France) and Sellafield (UK) were found to dominate the inventory of 129I in the Chinese sediments after 1990, not only the directly atmospheric releases of these reprocessing plants, but also re-emission of marine discharged 129I of these reprocessing plants in the highly contaminated European seas.
    No preview · Article · Apr 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: Protected species are the focus of many radiological environmental assessments. However, the lack of radioecological data for many protected species presents a significant international challenge. Furthermore, there are legislative restrictions on destructive sampling of protected species to obtain such data. Where data are not available, extrapolations are often made from ‘similar’ species but there has been little attempt to validate this approach.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: The chemical composition and isotopes of carbon and uranium were investigated in groundwater samples that were collected from 16 wells and 2 sources in the Northern Dvina Basin, Northwest Russia. Across the dataset, the temperatures in the groundwater ranged from 3.6 to 6.9 °C, the pH ranged from 7.6 to 9.0, the Eh ranged from -137 to +128 mV, the total dissolved solids (TDS) ranged from 209 to 22,000 mg L(-1), and the dissolved oxygen (DO) ranged from 0 to 9.9 ppm. The (14)C activity ranged from 0 to 69.96 ± 0.69 percent modern carbon (pmC). The uranium content in the groundwater ranged from 0.006 to 16 ppb, and the (234)U:(238)U activity ratio ranged from 1.35 ± 0.21 to 8.61 ± 1.35. The uranium concentration and (234)U:(238)U activity ratio increased from the recharge area to the redox barrier; behind the barrier, the uranium content is minimal. The results were systematized by creating a conceptual model of the Northern Dvina Basin's hydrogeological system. The use of uranium isotope dating in conjunction with radiocarbon dating allowed the determination of important water-rock interaction parameters, such as the dissolution rate:recoil loss factor ratio Rd:p (a(-1)) and the uranium retardation factor:recoil loss factor ratio R:p in the aquifer. The (14)C age of the water was estimated to be between modern and >35,000 years. The (234)U-(238)U age of the water was estimated to be between 260 and 582,000 years. The Rd:p ratio decreases with increasing groundwater residence time in the aquifer from n × 10(-5) to n × 10(-7) a(-1). This finding is observed because the TDS increases in that direction from 0.2 to 9 g L(-1), and accordingly, the mineral saturation indices increase. Relatively high values of R:p (200-1000) characterize aquifers in sandy-clayey sediments from the Late Pleistocene and the deepest parts of the Vendian strata. In samples from the sandstones of the upper part of the Vendian strata, the R:p value is ∼24, i.e., sorption processes are expressed more weakly, and uranium is possibly desorbed from the sediments. Overall, these results provide a better understanding of the evolution of uranium isotopes in groundwater systems.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: High concentrations of radionuclides and toxic elements in gold mine tailings facilities present a health hazard to the environment and people living near that area. Soil and water samples from selected areas around the Princess Mine dump were collected. Soil sampling was done on the surface (15 cm) and also 100 cm below the surface. Water samples were taken from near the dump, mid-stream and the flowing part of the stream (drainage pipe) passing through Roodepoort from the mine dump. Soil samples were analyzed by gamma-ray spectroscopy using a HPGe detector to determine the activity concentrations of 238U, 232Th and 4 40K from the activities of the daughter nuclides in the respective decay chains. The average activity concentrations for uranium and thorium in soil were calculated to be 129 ± 36.1 Bq/kg and 18.1 ± 4.01 Bq/kg, respectively. Water samples were analyzed using Inductively Coupled Plasma Mass Spectrometer. Transfer factors for uranium and thorium from soil to water (at point A closest to dump) were calculated to be 0.494 and 0.039, respectively. At point Z2, which is furthest from the dump, they were calculated to be 0.121 and 0.004, respectively. These transfer factors indicate that there is less translocation of the radionuclides as the water flows.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: This is the first study reporting recent sedimentation rates data (e.g. the past 120–150 years) for the Cruhlig Lake situated in the Danube Delta. The aim of this study is to analyse the recent sedimentation rates using the 210Pb dating method and identifying the heavy metal pollutants and their variability in time. Five sediment cores were taken with a gravity corer and – after drying the sliced samples–physical parameters, organic material and inorganic carbon content were determined. The total 210Pb content was measured via 210Po by alpha spectrometry, while supported 210Pb was measured by 226Ra (trough short life 222Rn daughters) with HPGe detectors. Heavy metals were determined by ICP-MS; from the 64 measured elements, only exceeding values of Al, As, Cd, Co, Cs, Cr, Cu, Fe, Hg, K, Li, Mg, Mn, Ni, Pb and Zn are discussed. After applying the CRS model, ages and sedimentation rates were calculated. The average sedimentation rate of the Cruhlig Lake is 0.21 ± 0.02 g/cm2y, Minimum values (0.05 ± 0.003 g/cm2y) are registered along the eastern shoreline of the lake before 1913, while maximum values are recorded due to the flooding in 2006 in the western side (1.34 ± 0.12 g/cm2y). Recent sedimentation rates divide the lake into three areas: the secluded eastern near shore part (0.63 ± 0.07 g/cm2y), the centre of the lake (0.92 ± 0.05 g/cm2y) and the dynamic western area, where most sediment transport takes place (1.13 ± 0.01 g/cm2y). The sedimentation pattern proves this lake to be very sensitive to fluvial discharge fluctuations. The building of the Iron Gate dams (1972 and 1985) had a negative impact on the sedimentation decreasing it with 58.74%, while after 1989 these values grew 2.25 times. The lake received a quantity of sediment rich in heavy metals in 1992 ± 3 y, which settled mostly on the eastern part. Values for Cd, Co, Cr, Hg, Pb and Zn are up to five times higher in 1980 ± 5 y in the eastern part of the lake, while Cd, Co, Cr and Ni are twice as high as the values measured for the marine substrate. Values of As show increasing of up to 150% in 2006 ± 2 y throughout the whole surface of the lake.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: After the accident at the Fukushima Dai-ichi Nuclear Power Plant owned by the Tokyo Electric Power Company on 11 March 2011, potassium fertilizer was applied to agricultural fields in the southern Tohoku and northern Kanto regions of Japan to reduce the uptake of radiocesium by crops. In this study, we examined the effects of two types of potassium fertilizers, potassium chloride (a readily available potassium fertilizer) and potassium silicate (a slow-release potassium fertilizer), as well as a split application of potassium, on the accumulation of 137Cs by rice plants in two pot experiments. The 137Cs concentrations in the brown rice and in the above-ground plants were significantly lower after potassium chloride application than after potassium silicate application. The potassium ion (K+) concentrations in soil solutions sampled 9 and 21 d after transplanting were significantly higher for the potassium chloride application than for the potassium silicate application. The K+ concentrations in soil solutions observed in the application of potassium silicate were similar to those in the treatment when no potassium was applied. This finding indicates that the application of potassium silicate did not sufficiently increase the available K+ for rice plants in the soil, which led to a greater uptake of 137Cs after the potassium silicate application than after the application of potassium chloride. The 137Cs concentration in brown rice was higher in the split application of potassium fertilizer with the second application at the full heading stage than that without split application and the split application with the second application before heading.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: With regard to environmental monitoring of certain nuclear facilities, pentavalent actinides, in particular neptunium and plutonium, play a key role, as the chief soluble, mobile forms of actinides. In the past five years, investigations carried out by hyphenating capillary electrophoresis to ICP–MS (CE–ICP–MS) have allowed a number of hitherto unknown thermodynamic data to be determined for Np(V) and Pu(V) interactions with the chief environmentally abundant anions. For the first time, data were provided for Pu(V) interactions with carbonate, sulfate, oxalate, chloride, and nitrate ions, allowing the Np(V)/Pu(V) analogy to be verified experimentally. Knowledge of Np(V) chemistry, especially in carbonate, and sulfate media, was also refined. These CE–ICP–MS studies, combined with some earlier findings, have brought about a renewal in the knowledge of An(V) chemistry in solution.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: We report results of measurements of isotopic ratios obtained with atom probe tomography on U3O8 reference materials certified for their isotopic abundances of uranium. The results show good agreement with the certified values. High backgrounds due to tails from adjacent peaks complicate the measurement of the integrated peak areas as well as the fact that only oxides of uranium appear in the spectrum, the most intense of which is doubly charged. In addition, lack of knowledge of other instrumental parameters, such as the dead time, may bias the results. Isotopic ratio measurements can be performed at the nanometer-scale with the expectation of sensible results. The abundance sensitivity and mass resolving power of the mass spectrometer are not sufficient to compete with magnetic-sector instruments but are not far from measurements made by ToF-SIMS of other isotopic systems. The agreement of the major isotope ratios is more than sufficient to distinguish most anthropogenic compositions from natural.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: A rapid method has been developed for the direct determination of radiostrontium (89Sr and 90Sr) released in seawater in the early phase of an accident. The method employs a fast and effective pre-concentration of radiostrontium by Sr–Ca co-precipitation followed by separation of radiostrontium using extraction chromatography technique. Radiostrontium is effectively separated in the presence of excessive dominant salts of seawater. Čerenkov and liquid scintillation assay (LSA) techniques are used to determine 89Sr and 90Sr. Sample preparation time is approximately 4 h for a set of 10 samples. The method was validated using spiked seawater samples at various activity ratios of 89Sr:90Sr ranging from 1:10 to 9:1. The mean chemical recovery of Sr was 85 ± 3%. 90Sr showed variable relative bias which enhanced with increasing ratio of 89Sr:90Sr and was in the range ±21%. The highest biases of 90Sr determination were due to lower activity concentrations of 90Sr and are regarded as acceptable in emergency situations with elevated levels of radiostrontium in the sample. The minimum detectable concentration (MDC) of 90Sr and 89Sr varied at different 89Sr:90Sr ratios. For 0.1 L seawater and 15 min counting time on a low background Hidex liquid scintillation counter (LSC), the MDC of 90Sr was in the range of 1.7–3.5 Bq L−1 and MDC of 89Sr was in the range 0.5–2.4 Bq L−1.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: Health Canada's Radiation Protection Bureau has identified trace quantities of 134Cs and 137Cs in commercially available green tea products of Japanese origin. Referenced to March 11, 2011, the activity ratio (134Cs/137Cs) has been determined to be 1:1, which supports an origin from the Fukushima Dai-ichi Nuclear Power Plant accident. The upper limits of typical tea beverage preparation conditions were applied to the most contaminated of these green tea samples to determine the proportion of radiocesium contamination that would be available for human consumption. The distribution of radiocesium among the components of the extraction experiments (water, residual tea solid, and filter media) was determined by both conventional and Compton-suppressed gamma spectroscopy. The latter aided tremendously in providing a more complete radiocesium distribution profile, particularly for the shorter-lived 134Cs. Cesium extraction efficiencies of 64 ± 7% and 64 ± 5% were determined based on 134Cs and 137Cs, respectively. Annual, effective dose estimates from ingestion of 137Cs and 134Cs (1.8-3.7 μSv), arising from the consumption of tea beverages prepared from the most contaminated of these samples, are insignificant relative to both total (~2.4 mSv) and ingested (~0.28 mSv) annual effective doses received from naturally occurring radioactive sources. As such, there is no health concern arising from the consumption of green tea beverages contaminated with radiocesium at the levels encountered in this study.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: The development of chemometric methods has substantially improved the quantitative usefulness of the fluorescence excitation-emission matrix (EEM) in the analysis of dissolved organic matter (DOM). In this study, Regional Integration Analysis (RIA) was used to quantitatively interpret EEMs and assess fluorescence quenching behavior in order to study the binding between uranyl ion and fulvic acid. Three fulvic acids including soil fulvic acid (SFA), Oyster River fulvic acid (ORFA) and Suwannee River fulvic acid (SRFA) were used and investigated by the spectroscopic techniques. The EEM spectra obtained were divided into five regions according to fluorescence structural features and two distinct peaks were observed in region III and region V. Fluorescence quenching analysis was conducted for these two regions with the stability constants, ligand concentrations and residual fluorescence values calculated using the Ryan-Weber model. Results indicated a relatively strong binding ability between uranyl ion and fulvic acid samples at low pH (log K value varies from 4.11 to 4.67 at pH 3.50). Fluorophores in region III showed a higher binding ability with fewer binding sites than in region V. Stability constants followed the order, SFA > ORFA > SRFA, while ligand concentrations followed the reverse order, SRFA > ORFA > SFA. A comparison between RIA and Parallel Factor Analysis (PARAFAC) data treatment methods was also performed and good agreement between these two methods (less than 4% difference in log K values) demonstrates the reliability of the RIA method in this study.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: Large quantities of radioactive materials were released into the air and the ocean as a result of the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, caused by the 2011 Tohoku earthquake and the subsequent major tsunami off the Pacific coast. There is much concern about radioactive contamination in both the watershed of the Abukuma River, which flows through Fukushima Prefecture, and its estuary, where it discharges into the sea in Miyagi Prefecture. We investigated radioactive cesium dynamics using mixing diagrams obtained from hydrographic observations of the Abukuma River Estuary. Particulate radioactive cesium dominates the cesium load in the river, whereas the dissolved form dominates in the sea. As the salinity increased from <0.1 to 0.1-2.3, the mixing diagram showed that dissolved radioactive cesium concentrations increased, because of desorption. Desorption from suspended particles explained 36% of dissolved radioactive cesium in estuarine water. However, the dissolved and particulate radioactive cesium concentrations in the sea decreased sharply because of dilution. It is thought that more than 80% of the discharged particulate radioactive cesium was deposited off the river mouth, where the radioactive cesium concentrations in sediment were relatively high (217-2440 Bq kg-1). Radioactive cesium that was discharged to the sea was transported southward by currents driven by the density distribution.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: The BAEC TRIGA research reactor (BTRR) is the only nuclear reactor in Bangladesh. Bangladesh Atomic Energy Regulatory Authority (BAERA) regulations require that nuclear reactor licensees undertake all reasonable precautions to protect the environment and the health and safety of persons, including identifying, controlling and monitoring the release of nuclear substances to the environment. The primary activation product of interest in terms of airborne release from the reactor is (41)Ar. (41)Ar is a noble gas readily released from the reactor stacks and most has not decayed by the time it moves offsite with normal wind speed. Initially (41)Ar is produced from irradiation of dissolved air in the primary water which eventually transfers into the air in the reactor bay. In this study, the airborne radioisotope (41)Ar generation concentration, ground level concentration and release rate from the BTRR bay region are evaluated theoretically during the normal reactor operation condition by several governing equations. This theoretical calculation eventually minimizes the doubt about radiological safety to determine the radiation level for (41)Ar activity whether it is below the permissible limit or not. Results show that the estimated activity for (41)Ar is well below the maximum permissible concentration limit set by the regulatory body, which is an assurance for the reactor operating personnel and general public. Thus the analysis performed within this paper is so much effective in the sense of ensuring radiological safety for working personnel and the environment.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: Research on nuclear technologies has been largely driven by a detachment of the 'technical content' from the 'social context'. However, social studies of science and technology - also for the nuclear domain - emphasize that 'the social' and 'the technical' dimensions of technology development are inter-related and co-produced. In an effort to create links between nuclear research and innovation and society in mutually beneficial ways, the Belgian Nuclear Research Centre started fifteen years ago a 'Programme of Integration of Social Aspects into nuclear research' (PISA). In line with broader science-policy agendas (responsible research and innovation and technology assessment), this paper argues that the importance of such programmes is threefold. First, their multi-disciplinary basis and participatory character contribute to a better understanding of the interactions between science, technology and society, in general, and the complexity of nuclear technology assessment in particular. Second, their functioning as (self -)critical policy supportive research with outreach to society is an essential prerequisite for policies aiming at generating societal trust in the context of controversial issues related to nuclear technologies and exposure to ionising radiation. Third, such programmes create an enriching dynamic in the organisation itself, stimulating collective learning and transdisciplinarity. The paper illustrates with concrete examples these claims and concludes by discussing some key challenges that researchers face while engaging in work of this kind.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: Food chain contamination with radiocaesium (RCs) in the aftermath of the Fukushima accident calls for an analysis of the specific factors that control the RCs transfer. Here, soil-to-plant transfer factors (TF) of RCs for grass were predicted from the potassium concentration in soil solution (mK) and the Radiocaesium Interception Potential (RIP) of the soil using existing mechanistic models. The mK and RIP were (a) either measured for 37 topsoils collected from the Fukushima accident affected area or (b) predicted from the soil clay content and the soil exchangeable potassium content using the models that had been calibrated for European soils. An average ammonium concentration was used throughout in the prediction. The measured RIP ranged 14-fold and measured mK varied 37-fold among the soils. The measured RIP was lower than the RIP predicted from the soil clay content likely due to the lower content of weathered micas in the clay fraction of Japanese soils. Also the measured mK was lower than that predicted. As a result, the predicted TFs relying on the measured RIP and mK were, on average, about 22-fold larger than the TFs predicted using the European calibrated models. The geometric mean of the measured TFs for grass in the affected area (N = 82) was in the middle of both. The TFs were poorly related to soil classification classes, likely because soil fertility (mK) was obscuring the effects of the soil classification related to the soil mineralogy (RIP). This study suggests that, on average, Japanese soils are more vulnerable than European soils at equal soil clay and exchangeable K content. The affected regions will be targeted for refined model validation.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity
  • [Show abstract] [Hide abstract]
    ABSTRACT: Understanding the behaviors of Cs+ in soils is crucial for evaluation of the impacts of disposal of soils contaminated by radiocesium, 137Cs. The desorption rate of Cs+ evaluated in relatively short periods of time may not be adequate for such a purpose. In this study, we investigated long-term desorption kinetics of 137Cs and 133Cs from soils collected in Fukushima Prefecture by batch desorption experiments in the presence of cation exchange resin as a sorbent. The sorbent can keep the concentration of Cs+ in the aqueous phase low and prevent re-sorption of desorbed Cs+. Up to 60% of 137Cs was desorbed after 139 d in dilute KCl media, which was larger than the desorption by conventional short-term extraction with 1 M ammonium acetate. Desorption of 137Cs continued even after this period. It was also found that high concentration of K+ prevented desorption of Cs+ in the initial stage of desorption, but the effect was alleviated with time. The desorbed fraction of stable Cs was smaller than that of 137Cs. This indicated that 137Cs may gradually move to more stable states in soils. The half-life of 137Cs desorption from the slowest sorption site was estimated to be at least two years by a three-site desorption model.
    No preview · Article · Mar 2016 · Journal of Environmental Radioactivity