Institute of Meteorology and Water Management, National Research Institute, Maritime Branch, Waszyngtona 42, 81-342 Gdynia, Poland. Electronic address: michal.saniewski@imgw.pl.
Radionuclides in the Arctic echinoderms have seldom been studied despite their considerable environmental importance. This manuscript covers the results of 90Sr and 137Cs measurements in common echinoderm taxa collected from the Svalbard Bank in the Barents Sea and from two High-Arctic fjords (Isfjorden and Magdalenefjorden). We focused on the echinoid, Strongylocentrotus droebachiensis, the asteroid, Henricia sanguinolenta, and the ophiuroid, Ophiopolis aculeata. For all echinoderms, the analysis revealed a negative correlation between 90Sr activity and the mass. Thus, we concluded that metals are accumulated faster at a young age when the growth is most rapid. The highest average activities of 137Cs followed the order O. aculeata>H. sanguinolenta>S. droebachiensis. This suggests that bioaccumulation was highly taxon-dependent and could reflect differences in the isotope exposures associated with the diet of echinoderms. The study provides a baseline for understanding radionuclide processes in the High-Arctic benthic echinoderm communities.
The river Iset belongs to the Techa-Iset-Tobol-Irtysh-Ob system contaminated by liquid radioactive wastes from Mayak plutonium facility in 1949-1956. This study represents the first retrospective analysis of postmortem measurements of 90Sr in bones from residents of the Iset riverside settlements in 1960-1982. It was shown that 90Sr concentration in bones of residents lived in settlements located downstream from the Techa river mouth (Shadrinsk, Isetskoye, Yalutorovsk) was 5 times higher than average 90Sr concentration in bones of the Russian residents. There was not statistically significant difference in accumulated 90Sr in bones between residents of the considered Iset' settlements indicating similar levels of 90Sr ingestion. Dietary 90Sr intake was reconstructed from the measurements of the radionuclide in bones. Total 90Sr dietary intake in 1950-1975 was 68 kBq; and 90% of the intake occurred in 1950-1961. In 1960s, 90Sr-contamination of the diet in settlements located downstream from the Techa river mouth was mostly (by 70%) due to global fallouts. Absorbed dose in the red bone marrow cumulated over 25 years of exposure was equal to 14 (4.7-42) mGy.
The quantity of the long lived (half-life 15.7 million years) radioactive isotope 129I in the pre-nuclear age ocean was approximately 100 kg. Various nuclear related activities, including weapons testing, nuclear fuel reprocessing, Chernobyl and other authorized or non-authorized dumping of radioactive waste have increased the ocean inventory of 129I by more than one order of magnitude. The most important of these sources are the direct marine discharges from the commercial reprocessing facilities at La Hague (France) and Sellafield (UK) which have discharged approximately 1640 kg in the English Channel, and approximately 720 kg in the Irish Sea, respectively. We discuss how this 129I can be used as both a 'pathway' and 'transit time' tracer in the North Atlantic and Arctic oceans, as well as a parameter for distinguishing between reprocessed and non-reprocessed nuclear waste in the ocean, and as a proxy for the transport and dilution of other soluble pollutants input to the North Sea.
This research work is devoted to analyzing the processes of accumulation and distribution of long-lived radionuclides of 90Sr and 137Cs in the components of water-sediment-macrophytes of Lake Malye Kirpichiky (Chelyabinsk region). The characteristic features of redistribution of radioactive substances, depending on the texture of the bottom sediments of the lake and the species composition of aquatic vegetation are shown. Also shown is the total stock of radionuclides in water and bottom sediments. The coefficients of 90Sr and 137Cs accumulation in bottom sediments and macrophytes have been calculated.
Accumulation of artificial and natural radionuclides in the chains of food webs leading to non-predatory and piscivorous fish of the Yenisei River was investigated during one year before and three years after the shutdown of a nuclear power plant at the Mining-and-Chemical Combine (2009-2012). The activity of artificial radionuclides in the samples of biota ofthe Yenisei River (aquatic moss, gammarids, dace, grayling, pike) was estimated. The concentration of radionuclides with induced activity (51Cr, 54Mn, 58Co, 60Co, 65Zn, 141, 144Ce, 152, 154Eu, 239Np) decreased in the biomass of biota after the shutdown of the nuclear power plant; the concentration of 137Cs did not. Analysis of the accumulation factors (C(F)) allows us to expect the effective accumulation of 137Cs in the terminal level of the food web of the Yenisei River--pike (C(F) = 2.0-9.4), i.e. biomagnifications of radiocesium. Accumulation of artificial, radionuclides in non-predatory fish from gammarids was not effective (C(F)
The activity concentrations of (226)Ra and (228)Ra in drinking water were determined in water samples from 176 drilled wells. (226)Ra activity concentrations were in the range of
Waterborne radioactive releases into the Techa River from the Mayak Production Association in Russia during 1949-1956 resulted in significant doses to about 30,000 persons who lived in downstream settlements. The residents were exposed to internal and external radiation. Two methods for reconstruction of the external dose are considered in this paper, electron paramagnetic resonance (EPR) measurements of teeth, and fluorescence in situ hybridization (FISH) measurements of chromosome translocations in circulating lymphocytes. The main issue in the application of the EPR and FISH methods for reconstruction of the external dose for the Techa Riverside residents was strontium radioisotopes incorporated in teeth and bones that act as a source of confounding local exposures. In order to estimate and subtract doses from incorporated (89,90)Sr, the EPR and FISH assays were supported by measurements of (90)Sr-body burdens and estimates of (90)Sr concentrations in dental tissues by the luminescence method. The resulting dose estimates derived from EPR to FISH measurements for residents of the upper Techa River were found to be consistent: The mean values vary from 510 to 550 mGy for the villages located close to the site of radioactive release to 130-160 mGy for the more distant villages. The upper bound of individual estimates for both methods is equal to 2.2-2.3 Gy. The EPR- and FISH-based dose estimates were compared with the doses calculated for the donors using the most recent Techa River Dosimetry System (TRDS). The TRDS external dose assessments are based on the data on contamination of the Techa River floodplain, simulation of air kerma above the contaminated soil, age-dependent lifestyles and individual residence histories. For correct comparison, TRDS-based doses were calculated from two sources: external exposure from the contaminated environment and internal exposure from (137)Cs incorporated in donors' soft tissues. It is shown here that the TRDS-based absorbed doses in tooth enamel and muscle are in agreement with EPR- and FISH-based estimates within uncertainty bounds. Basically, this agreement between the estimates has confirmed the validity of external doses calculated with the TRDS.
In this study the solid cancer mortality data in the Techa River Cohort in the Southern Urals region of Russia was analyzed. The cohort received protracted exposure in the 1950s due to the releases of radioactive materials from the Mayak plutonium complex. The Extended Techa River Cohort includes 29,849 people who resided along the Techa River between 1950 and 1960 and were followed from January 1, 1950 through December 31, 1999. The analysis was done within the framework of the biologically based two-stage clonal expansion (TSCE) model. It was found that about 2.6% of the 1854 solid cancer deaths (excluding 18 bone cancer cases) could be related to radiation exposure. At age 63, which is the mean age for solid cancer deaths, the excess relative risk (ERR) and excess absolute risk (EAR) were found to be 0.76 Gy(-1) (95% CI 0.23; 1.29) and 33.0 (10(4) PY Gy)(-1) (95% CI 9.8; 52.6), respectively. These risk estimates are consistent with earlier excess relative risk analyses for the same cohort. The change in the ERR with age was investigated in detail, and an increase in risk with attained age was observed. Furthermore, the data were tested for possible signs of genomic instability, and it was found that the data could be described equally well by a model incorporating effects of genomic instability. Results from the TSCE models indicated that radiation received at older ages might have stronger biological effects than exposure at younger ages.
Population exposure in the Urals region occurred due to the releases of radionuclides by the Mayak plutonium facility in the 1950's. The major sources of radioactive contamination were the discharges of liquid wastes into the Techa river (1949-1956); an explosion in the storage facility for high level radioactive wastes which formed the East Urals Radioactive Trace in 1957; and gaseous aerosol releases within the first decade of the facility's operation (1949-1957). The problems of dose reconstruction for the population exposed on the Techa river banks and East Urals Radioactive Trace are outlined. The initial data sets and basic models for dose reconstruction are described. The main tasks of the Techa River Dosimetry System Project and the approaches to individual internal and external dose reassessment are formulated.
A numerical model simulation has been used to predict extent and variability in the anthropogenic (129)I pollution in the Arctic Ocean and Nordic Seas region over a period of 100 years. The source function of (129)I used in the model is represented by a well-known history of discharges from the Sellafield and La Hague nuclear reprocessing facilities. The simulations suggest a fast transport and large inventory of the anthropogenic (129)I in the Arctic and North Atlantic Oceans. In a fictitious case of abrupt stop of the discharges, a rapid decline of inventories is observed in all compartments except the North Atlantic Ocean, the deep Nordic Seas and the deep Arctic Ocean. Within 15 years after the stop of releases, the model prediction indicates that near-equilibrium conditions are reached in all compartments.