The surface of small glaciers as radioactive hotspots: Concentration of radioisotopes during predicted intensive melting in the Alps.

Glaciers are considered secondary sources of pollutants, including radioisotopes such as Cesium or Plutonium, with heightened concentrations compared to other ecosystems. The predicted melting of glaciers poses a substantial risk of releasing stored radioisotopes, yet understanding the glacier-specific factors influencing their concentration remains limited. This study investigates the relationship between glacier altitude, surface area, organic matter content in dark supraglacial sediment (cryoconite), precipitation, and activity concentrations of natural (210Pb) and anthropogenic radionuclides (137Cs and 241Am) across 19 Alpine glaciers. Results indicate that radioisotope concentrations depend on organic matter content in the cryoconite, highlighting the role of biotic-abiotic interactions in pollutant accumulation on glaciers. Moreover, 210Pb activity concentration decreases with glacier altitude, likely due to atmospheric variations in 222Rn. Water precipitation events, such as during peaks in 137Cs deposition and after the Chernobyl Nuclear Power Plant disaster, do not impact current activity concentrations. Importantly, radioisotope concentrations in cryoconite are higher on smaller glaciers. This directly supports the hypothesis that the cryoconite retains a significant share of radioisotopes stored in the ice during intensive melting. Since many small glaciers in the Alps are predicted to disappear within the next 50 years, we anticipate release of radioisotopes to mountain ecosystems might be higher than previously forecasted.

Cosmogenic 22Na, 7Be and terrestrial 137Cs, 40K radionuclides in ground level air samples collected weekly in Kraków (Poland) over years 2003-2006.

A low background gamma spectrometer with an Etruscan, 2500 years old lead shield and a muon veto detector were applied to study 22Na and 7Be activity concentration in ground level air aerosol samples collected weekly over the years 2003-2006 in Kraków. Each sample was formed with ca 100 000 m3 of passed air, collected with two parallel ASS-500 high volume air samplers. The results for 40K and 137Cs are also presented for reference and comparison. Presented frequency distributions for activity concentration and correlation between the obtained results are discussed. The activity concentration results confirmed seasonal variation of activity to be different for all the investigated radionuclides. Moreover, the seasonal variation in nucleus activity ratio was also noticed for 22Na and 7Be. Cosmogenic radionuclides being mainly of stratospheric origin, are subsequently attached to fine aerosols, via which they are transported to the ground level air. The mean aerosol transport time within the troposphere was estimated as equal to 7.5 days on average, reaching even 50 days in warm seasons. Limitations of the applied model were identified.

137Cs and 40K in fruiting bodies of different fungal species collected in a single forest in southern Poland.

Fruiting bodies of fungi belonging to more than 70 species were collected within a few thousand square meter area of one forest during 2006 and 2007. The soil profile was collected to check the cumulative deposition of (137)Cs, which was relatively high, equal to 64 +/- 2 kBq/m(2) (calculated for October 2006). The majority of this activity was in the first 6 cm. Fruitbodies were analyzed for radiocesium and (40)K by means of gamma-spectrometry. The highest (137)Cs activity was 54.1 +/- 0.7 kBq/kg (dry weight) for a sample of Lactarius helvus collected in 2006. The results for 2006 were higher than those for 2007. In a few cases the traces of short-lived (T(1/2) = 2.06 a) (134)Cs were still found in samples. The importance of mycorrhizal fungi for radiocesium accumulation is confirmed. The differences in activity among the species are discussed in relation to observations and predictions from previous studies, where the change in relative accumulation between fruiting bodies of different species was at least partially explained by the differences in the depth of the mycelium localization in a litter/soil system. It is concluded that in some cases, such as Boletus edulis and Xerocomus badius, this prediction is fulfilled and therefore this explanation confirmed.

Plutonium, 137Cs and 90Sr in selected invertebrates from some areas around Chernobyl nuclear power plant.

Results are presented for (137)Cs, (90)Sr and plutonium activity concentrations in more than 20 samples of terrestrial invertebrates, including species of beetles, ants, spiders and millipedes, collected in the highly contaminated area of the Chernobyl exclusion zone. The majority of samples were collected in Belarus, with some also collected in the Ukraine. Three other samples were collected in an area of lower contamination. Results show that seven samples exceed an activity concentration of 100 kBq/kg (ash weight--a.w.) for (137)Cs. The maximum activity concentration for this isotope was 1.52+/-0.08 MBq/kg (a.w.) determined in ants (Formica cynerea). Seven results for (90)Sr exceeded 100 kBq/kg (a.w.), mostly for millipedes. Relatively high plutonium activity concentrations were found in some ants and earth-boring dung beetles. Analyses of activity ratios showed differences in transfer of radionuclides between species. To reveal the correlation structure of the multivariate data set, the Partial Least-Squares method (PLS) was used. Results of the PLS model suggest that high radiocesium activity concentrations in animal bodies can be expected mainly for relatively small creatures living on the litter surface. In contrast, high strontium activity concentrations can be expected for creatures which conduct their lives within litter, having mixed trophic habits and a moderate lifespan. No clear conclusions could be made for plutonium.

Substituent effects on the electrophilic activity of nitroarenes in reactions with carbanions.

The effect on electrophilic activity of substituents located para, ortho, and meta to the nitro group of nitrobenzenes was determined by using vicarious nucleophilic substitution of hydrogen (VNS) with the carbanion of chloromethyl phenyl sulfone (1) as the model process. Values for the relative activities of substituted nitroarenes are given relative to nitrobenzene, which was taken as the standard. This process was chosen as a model reaction because it meets key criteria, such as the wide range of substituents that can be present on the nitrobenzene ring, a low sensitivity to steric hindrance, and in particular the possibility of ensuring conditions in which the overall relative rates of reaction in competitive experiments are equal to the relative rates of nucleophilic addition. The values of relative rates of addition, which were taken to be a measure of electrophilic activity, were determined by competitive experiments in which pairs of nitroarenes competed for the VNS reaction with carbanion of 1. A comprehensive set of data for effects of substituents on the electrophilic activity of nitroarenes is presented for the first time.

Reactions of nitroheteroarenes with carbanions: bridging aromatic, heteroaromatic, and vinylic electrophilicity.

The relative rate constants for the vicarious nucleophilic substitution (VNS) of the anion of chloromethyl phenyl sulfone (1-) with a variety of nitroheteroarenes, for example, nitropyridines, nitropyrroles, nitroimidazoles, 2-nitrothiophene, and 4-nitropyrazole, have been determined by competition experiments. It was shown that nitropyridines are approximately four orders of magnitude more reactive than nitrobenzene. Among the five-membered heterocycles 2-nitrothiophene is the most active followed by nitroimidazoles and 4-nitropyrazole. Nitropyrroles are the least electrophilic nitroheteroarenes with reactivities comparable to nitrobenzene. Quantum chemically calculated methyl anion affinities (B3LYP/6-311G(d,p)//B3LYP/6-31G(d)) of the nitroarenes correlated only moderately with the partial relative rate constants. The correlation of these activities with the LUMO energies of nitroarenes is even worse. By measuring the second-order rate constants of the addition of 1- to nitroarenes and to diethyl arylidenemalonates 10, it was possible to link the electrophilic reactivities of nitroheteroarenes with the comprehensive electrophilicity scale based on the linear-free-energy-relationship log k(20 degrees C)=s(N+E).

Traces of DU in samples of environmental bio-monitors (non-flowering plants, fungi) and soil from target sites of the Western Balkan region.

This paper reports results of gamma and alpha spectrometric measurements for mosses, lichens, fungi and soil samples from areas in the Balkans targeted by depleted uranium (DU). Samples were collected in 2002 and 2003 in the vicinity of several villages, principally Han Pijesak (Bosnia and Herzegovina, hit by DU in 1995) and Bratoselce (South Serbia, hit by DU in 1999) and in lesser numbers from Gornja Stubla, Kosovo (which is identified as a high natural radon/thoron area) and Presevo close to the Kosovo border. In the course of gamma spectrometric measurements some results suggested samples with unusual high uranium contents which might be considered to be a signature for the presence of DU, although many samples had very high detection limits. Alpha spectrometric measurements directly proved the presence of DU for five samples, all from directly targeted places. These were samples of mosses, lichens and soil. For some samples homogeneity tests were applied which showed a rather even distribution of DU in these samples. No trace of DU was found in any sample from a dwelling.