Level, distribution and sources of Np, Pu and Am isotopes in Peter the Great Bay of Japan sea.

Transuranium elements such as Np, Pu and Am, are considered to be the most important radioactive elements in view of their biological toxicity and environmental impact. Concentrations of 237Np, Pu isotopes and 241Am in two sediment cores collected from Peter the Great Bay of Japan Sea were determined using radiochemical separation combined with inductively coupled plasma mass spectrometry (ICP-MS) measurement. The 239,240Pu and 241Am concentrations in all sediment samples range from 0.01 Bq/kg to 2.02 Bq/kg and from 0.01 Bq/kg to 1.11 Bq/kg, respectively, which are comparable to reported values in the investigated area. The average atomic ratios of 240Pu/239Pu (0.20 ± 0.02 and 0.21 ± 0.01) and 241Am/239+240Pu activity ratios (3.32 ± 2.76 and 0.45 ± 0.17) in the two sediment cores indicated that the sources of Pu and Am in this area are global fallout and the Pacific Proving Grounds through the movement of prevailing ocean currents, and no measurable release of Np, Pu and Am from the local K-431 nuclear submarine incident was observed. The extremely low 237Np/239Pu atomic ratios ((2.0-2.5) × 10-4) in this area are mainly attributed to the discrepancy of their different chemical behaviors in the ocean due to the relatively higher solubility of 237Np compared to particle active plutonium isotopes. It was estimated using two end members model that 23% ± 6% of transuranium radionuclides originated from the Pacific Proving Grounds tests, and the rest (ca. 77%) from global fallout.

Radionuclides' Recovery from Seawater Using FIC and FIC A Sorbents.

To solve radioecological and oceanological problems (estimate the vertical transport, flows of particulate organic carbon, phosphorus biodynamics, submarine groundwater discharge, etc.), it is necessary to determine the natural values of the radionuclides' activity in seawater and particulate matter. For the first time, the radionuclides' sorption from seawater was studied using sorbents based on activated carbon modified with iron(III) ferrocyanide (FIC) and based on activated carbon modified with iron(III) hydroxide (FIC A-activated FIC) obtained by FIC sorbent treatment with sodium hydroxide solution. The possibility of trace amounts of phosphorus, beryllium, and cesium recovery in laboratory conditions has been investigated. Distribution coefficients, dynamic, and total dynamic exchange capacities were determined. The physicochemical regularities (isotherm and kinetics) of sorption have been studied. The results obtained are characterized via Langmuir, Freindlich, and Dubinin-Radushkevich isotherm equations, as well as pseudo-first and pseudo-second-order kinetic models, intraparticle diffusion, and the Elovich model. Under expeditionary conditions, the sorption efficiency of 137Cs using FIC sorbent, 7Be, 32P, and 33P-using FIC A sorbent with a single-column method by adding a stable tracer, as well as the sorption efficiency of radionuclides 210Pb and 234Th with their natural content by FIC A sorbent in a two-column mode from large volumes of seawater was assessed. High values of efficiency of their recovery by the studied sorbents were achieved.

The anthropogenic fallout radionuclides in soils of Mount Khuko (the Western Caucasus) and their application for determination of sediment redistribution.

The purposes of this study are to determine the content and origin of anthropogenic fallout radionuclides (FRN) in soils of Mount Khuko, located in the western sector of the Caucasus Mountains and to assess the possibility to use them for evaluation of sediment redistribution for the alpine grasslands,. The field study was carried out in August 2019 near the top of Mount Khuko, located in the western part of the main Caucasus Mountain Ridge. Integral and incremental soil samples were collected from the different morphological units of the studied area. The content of 137Cs and 241Am in soil samples was evaluated using laboratory gamma-spectrometry. A part of samples was selected for Pu isotopes extraction and then alpha-spectrometric analysis. It was established that the 137Cs contamination of soils in the studied area has at least two sources of origin. The first source is the 137Cs bomb-derived fallout after the bomb tests in 1950-60th, which is widespread across the globe. The second source is 137Cs Chernobyl-derived fallout High random variability (Cv = 25-42%) was found within reference sites, located at the undisturbed areas on the local flat interfluves due to high variability of soil characteristics (grain size, density, organic matter content etc.). However minimum spatial variability (range 12,2-14,3 kBq/m2) was identified for the mean value of 137Cs inventories for all 5 reference sites located in the different parts of the studied area. It is difficult to separate individual peaks of the bomb-derived and Chernobyl-derived 137Cs falloutin sediment sinks with low sedimentation rates. Application 239,240Pu as an additional chronological marker allows to identify the origin of above mention peaks in the soils of alpine grasslands and of dry lake bottom.

Use of natural and artificial radionuclides to determine the sedimentation rates in two North Caucasus lakes.

The specific activities of natural (210Pb, 226Ra, and 232Th) and artificial (137Cs, 239,240Pu, and 241Am) radionuclides in the sediments of two North Caucasus lakes were determined. The two lakes, Lake Khuko and Lake Donguz-Orun, differ in their sedimentation conditions. Based on the use of unsupported 210Pbex and both Chernobyl-derived and bomb-derived 137Cs as chronological markers, it was established that the sedimentation rates in Lake Khuko over the past 55-60 y did not exceed 0.017 cm y-1. Sedimentation rates in Lake Donguz-Orun were found to be more than an order of magnitude higher. In the latter case, the sedimentation rates for the period from 1986 to the present were over 1.5 times higher than they were for the period 1963-1986. The differences in sedimentation rates were due to differences in the rates of denudation of their respective catchment areas. The specific activities of artificial radionuclides (137Cs, 2600 Bq kg-1; 239,240Pu, 162 Bq kg-1; and 241Am, 36 Bq kg-1) and their ratios in the sediments of Lake Khuko show that their deposition was mainly due to global stratospheric fallout of technogenic radionuclides associated with nuclear bomb testing during 1954-1963-rather than fallout from the Chernobyl accident. Several factors, including the mode of precipitation, features of the surface runoff, and location of Lake Khuko, were responsible for the accumulation of artificial radionuclides.