Plutonium isotopes in the ground air layer in southern Poland (2010-2016): Source terms, seasonal variability and correlations with meteorological conditions.

In this study, the results of the analysis of Pu-238 and Pu-239 + 240 activity concentrations on aerosol filters collected from 2010 to 2016 in Krakow (Southern Poland) are presented and discussed. For the first time, the temporal variation of Pu-239 + 240 activity concentration in surface air in Poland was studied using Fourier analysis. The analysis clearly showed that the Pu-239 + 240 content in the near-ground air layer is subject to seasonal variations and demonstrates annual periodicity. Pu analyses were performed using alpha spectrometry. The measured values ranged from 1.93∙10-10 Bq/m3 to 1.31∙10-8 Bq/m3 with an average of 2.07∙10-9 Bq/m3 for Pu-239 + 240 and from 9.07∙10-11 Bq/m3 to 1.27∙10-9 Bq/m3 with the average 1.52∙10-10 Bq/m3 for Pu-238. The analysis of the potential sources of plutonium isotopes in the air aerosols samples indicated that only two samples are uniquely characterized by the ratio corresponding to spent nuclear fuel: February 2012 (0.59 ± 0.18) and February 2015 (0.68 ± 0.19). The remaining samples showed mixed origins, with global radioactive fallout appearing to contribute more than spent nuclear fuel. To study the relationship between Pu-239 + 240 and meteorological conditions, Pearson's correlation and circulation pattern analyses were performed. The analyses showed that the Pu-239 + 240 activity concentration depends on air temperature (R = 0.51), the sum of ice and snowfall (R = -0.45), relative humidity (R = -0.54) and mean total cloud cover (R = -0.56). High concentrations of Pu-239 + 240 were positively correlated with air advection from the southern and eastern sectors, whereas low concentrations were observed during dynamic weather conditions with intense circulation from the western sector. In case of Pu-238 no significant correlation was observed.

Air radioactivity in Marambio Base: The peculiar character of Antarctic Peninsula.

The Antarctic region is considered to be the least contaminated in the world due to its specific location and separation of this area as well as low activity of humans (Hashimoto et al., 1988). Additionally, in accordance with the provision of the Antarctic Treaty System (Antarctic Treaty Secretariat, 2020) it is prohibited to conduct any actions with nuclear materials in this area. Nevertheless, Antarctica is not free from radioactive pollutants (human activity, nuclear tests or accidents) created in other parts of the world and transported by air masses or sea currents to the region of the South Pole where they can be detected. This paper presents results of measurements of activity concentrations of both natural and artificial gamma-ray emitting isotopes present on air-filters exposed in the ground level of the air in Marambio Base (Antarctic Peninsula). Furthermore, comparison with results obtained from other part of Antarctica were performed (i.e. Aboa Station, including radioisotope sources estimation). Investigation suggests that the northern part of the Antarctic Peninsula is effectively isolated from the Antarctic mainland and, in case of air radioactivity, should be considered separately.

Europe-Wide Atmospheric Radionuclide Dispersion by Unprecedented Wildfires in the Chernobyl Exclusion Zone, April 2020.

From early April 2020, wildfires raged in the highly contaminated areas around the Chernobyl nuclear power plant (CNPP), Ukraine. For about 4 weeks, the fires spread around and into the Chernobyl exclusion zone (CEZ) and came within a few kilometers of both the CNPP and radioactive waste storage facilities. Wildfires occurred on several occasions throughout the month of April. They were extinguished, but weather conditions and the spread of fires by airborne embers and smoldering fires led to new fires starting at different locations of the CEZ. The forest fires were only completely under control at the beginning of May, thanks to the tireless and incessant work of the firefighters and a period of sustained precipitation. In total, 0.7-1.2 TBq 137Cs were released into the atmosphere. Smoke plumes partly spread south and west and contributed to the detection of airborne 137Cs over the Ukrainian territory and as far away as Western Europe. The increase in airborne 137Cs ranged from several hundred µBq·m-3 in northern Ukraine to trace levels of a few µBq·m-3 or even within the usual background level in other European countries. Dispersion modeling determined the plume arrival time and was helpful in the assessment of the possible increase in airborne 137Cs concentrations in Europe. Detections of airborne 90Sr (emission estimate 345-612 GBq) and Pu (up to 75 GBq, mostly 241Pu) were reported from the CEZ. Americium-241 represented only 1.4% of the total source term corresponding to the studied anthropogenic radionuclides but would have contributed up to 80% of the inhalation dose.

Gamma emitters in atmospheric precipitation in Krakow (Southern Poland) during the years 2005-2015.

The results of the sum of dry and wet activity deposition for naturally occurring 7Be, 210Pb, 40K, 22Na and anthropogenic 137Cs radionuclides in Krakow (Southern Poland) for the samples collected over 10 years (from August 2005 to July 2015) are presented and discussed. The radionuclides were determined using low background gamma spectrometry with HPGe detectors. Additionally, in this paper there are shown the results of activity concentrations in water from air precipitation for 7Be, 210Pb, 22Na, 40K and 137Cs radioisotopes from the period of 7 years (from August 2008 to July 2015). For all these series the statistical analysis including Spearman correlations, effects of seasonal variation and multiple regression models were conducted. After excluding two months from 2011 affected by the Fukushima accident, high Spearman correlation factors (R > 0.5) for activity deposition were noticed for the pair of the cosmogenic radionuclides 7Be and 22Na (R = 0.508) and between 210Pb and 7Be (R = 0.570). High correlation was noted between activity deposition and amount of precipitation for 7Be (R = 0.677). The seasonal correlations between 7Be-22Na, 40K-137Cs, 210Pb-137Cs and 7Be-210Pb were investigated and the highest correlation coefficient R = 0.731 for the 40K-137Cs pair was in the spring season. High correlations were observed also between 210Pb and 7Be for autumn (R = 0.594), 40K-137Cs in summer (R = 0.582), 7Be-22Na in spring (R = 0.635) and 210Pb-137Cs in autumn (R = 0.672). The multiple regression approach showed the interesting difference in scavenging mechanisms of cosmogenic and terrestrial radionuclides. According to that model, the deposition of cosmogenic nuclides was noticeably related to the amount of precipitation, while the deposition of terrestrial radionuclides did not show such dependence.

Combined, sequential procedure for determination of 137Cs, 40K, 63Ni, 90Sr, 230,232Th, 234,238U, 237Np, 238,239+240Pu and 241Am applied for study on contamination of soils near Zarnowiec Lake (northern Poland).

The paper summarizes results of investigation of the current state of radioactive contamination on site being under consideration for planned nuclear power plant in northern Poland. Thanks to use of sequential procedure it was possible to determine activity concentrations for radioisotopes of nine elements, both natural and artificial. Results show that observed levels of radioactive contamination are rather typical for central Europe and global fallout is dominant factor of presence of artificial radionuclides. The total deposition for artificial radionuclides revealed maxima equal to 1747 ± 121 Bq/m2 for 137Cs, 3854 ± 158 Bq/m2 for 90Sr, 101 ± 23 mBq/m2 for 237Np, 57.7 ± 6.0 Bq/m2 for 241Am, 3.27 ± 0.80 Bq/m2 for 238Pu and 68.5 ± 5.0 Bq/m2 for 239+240Pu.

Plutonium isotopes in the atmosphere of Central Europe: Isotopic composition and time evolution vs. circulation factors.

This paper reports evidence of Pu isotopes in the lower part of the troposphere of Central Europe. The data were obtained based on atmospheric aerosol fraction samples collected from four places in three countries (participating in the informal European network known as the Ring of Five (Ro5)) forming a cell with a surface area of about 200,000km(2). We compared our original data sets from Krakow (Poland, 1990-2007) and Bialystok (Poland, 1991-2007) with the results from two other locations, Prague (Czech Republic; 1997-2004) and Braunschweig (Germany; 1990-2003) to find time evolution of the Pu isotopes. The levels of the activity concentration for (238)Pu and for ((239+240))Pu were estimated to be a few and some tens of nBqm(-3), respectively. However, we also noted some results were much higher (even about 70 times higher) than the average concentration of (238)Pu in the atmosphere. The achieved complex data sets were used to test a new approach to the problem of solving mixing isotopic traces from various sources (here up to three) in one sample. Results of our model, supported by mesoscale atmospheric circulation parameters, suggest that Pu from nuclear weapon accidents or tests and nuclear burnt-up fuel are present in the air.