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.

Climate-induced hydrological fluctuations shape Arctic Alaskan peatland plant communities.

Rapidly increasing temperatures in high-latitude regions are causing major changes in wetland ecosystems. To assess the impact of concomitant hydroclimatic fluctuations, mineral deposition, and autogenous succession on the rate and direction of changing arctic plant communities in Arctic Alaska, we conducted detailed palaeoecological analyses using plant macrofossil, pollen, testate amoebae, elemental analyses, and radiocarbon and lead (210Pb) dating on two replicate monoliths from a peatland that developed in a river valley on the northern foothills of the Books Range. We observed an expansion of Sphagnum populations and vascular plants preferring dry habitats, such as Sphagnum warnstorfii, Sphagnum teres/squarrosum, Polytrichum strictum, Aulacomnium palustre and Salix sp., in recent decades between 2000 and 2015 CE, triggered by an increase in temperature and deepening water tables. Deepening peatland water tables became accentuated over the last two decades, when it reached its lowest point in the last 700 years. Conversely, a higher water-table between ca. 1500 and 1950 CE led to a recession of Sphagnum communities and an expansion of sedges. The almost continuous supply of mineral matter during this time led to a dominance of minerotrophic plant communities, although with varying species composition throughout the study period. The replicate cores show similar patterns, but nuanced differences are also visible, depicting fine spatial scale differences particularly in peat-forming plant distribution and the different timings of their presence. In conclusion, our study provides valuable insights into the impact of hydroclimatic fluctuations on peatland vegetation in Arctic Alaska, highlighting their tendency to dry out in recent decades. It also highlights the importance of river valley peatlands in paleoenvironmental reconstructions.

Global variability and controls on the accumulation of fallout radionuclides in cryoconite.

The accumulation of fallout radionuclides (FRNs) from nuclear weapons testing and nuclear accidents has been evaluated for over half a century in natural environments; however, until recently their distribution and abundance within glaciers have been poorly understood. Following a series of individual studies of FRNs, specifically 137Cs, 241Am and 210Pb, deposited on the surface of glaciers, we now understand that cryoconite, a material commonly found in the supraglacial environment, is a highly efficient accumulator of FRNs, both artificial and natural. However, the variability of FRN activity concentrations in cryoconite across the global cryosphere has never been assessed. This study thus aims to both synthesize current knowledge on FRNs in cryoconite and assess the controls on variability of activity concentrations. We present a global database of new and previously published data based on gamma spectrometry of cryoconite and proglacial sediments, and assess the extent to which a suite of environmental and physical factors can explain spatial variability in FRN activity concentrations in cryoconite. We show that FRNs are not only found in cryoconite on glaciers within close proximity to specific sources of radioactivity, but across the global cryosphere, and at activity concentrations up to three orders of magnitude higher than those found in soils and sediments in the surrounding environment. We also show that the organic content of cryoconite exerts a strong control on accumulation of FRNs, and that activity concentrations in cryoconite are some of the highest ever described in environmental matrices outside of nuclear exclusion zones, occasionally in excess of 10,000 Bq kg-1. These findings highlight a need for significant improvements in the understanding of the fate of legacy contaminants within glaciated catchments. Future interdisciplinary research is required on the mechanisms governing their accumulation, storage, and mobility, and their potential to create time-dependent impacts on downstream water quality and ecosystem sustainability.

Unveiling the extreme environmental radioactivity of cryoconite from a Norwegian glacier.

This study is a first survey of the occurrence of artificial (137Cs, 241Am, 207Bi, Pu isotopes) and natural (210Pb, 228Ac, 214Bi, 40K) radionuclides in Norwegian cryoconite. Cryoconite samples were collected before (12 samples) and after (5 samples) a rainfall event, after which 7 cryoconite holes dissapeared. The concentrations of radionuclides in cryoconite samples from the Blåisen Glacier are compared with data from the Arctic and Alpine glaciers. Cryoconite samples from the studied glacier had extremely high activity concentrations of 137Cs, 241Am, 207Bi and 239+240Pu (up to 25,000 Bq/kg, 58 Bq/kg, 13 Bq/kg and 131 Bq/kg, respectively) and also high concentrations of organic matter (OM), comparing to other Scandinavian and Arctic glaciers, reaching up to ~40% of total mass. The outstandingly high concentrations of 137Cs, 241Am, Pu isotopes, and 207Bi on the Blåisen Glacier are primarily related to bioaccumulation of radionuclides in organic-rich cryoconite and might be enhanced by additional transfers of contamination from the tundra by lemmings during their population peaks. The presumed influence of intense rainfall on radionuclide concentrations in the cryoconite was not confirmed.

Cryoconite - From minerals and organic matter to bioengineered sediments on glacier's surfaces.

Cryoconite is a mixture of mineral and organic material covering glacial ice, playing important roles in biogeochemical cycles and lowering the albedo of a glacier surface. Understanding the differences in structure of cryoconite across the globe can be important in recognizing past and future changes in supraglacial environments and ice-organisms-minerals interactions. Despite the worldwide distribution and over a century of studies, the basic characteristics of cryoconite, including its forms and geochemistry, remain poorly studied. The major purpose of our study is the presentation and description of morphological diversity, chemical and photoautotrophs composition, and organic matter content of cryoconite sampled from 33 polar and mountain glaciers around the globe. Observations revealed that cryoconite is represented by various morphologies including loose and granular forms. Granular cryoconite includes smooth, rounded, or irregularly shaped forms; with some having their surfaces covered by cyanobacteria filaments. The occurrence of granules increased with the organic matter content in cryoconite. Moreover, a major driver of cryoconite colouring was the concentration of organic matter and its interplay with minerals. The structure of cyanobacteria and algae communities in cryoconite differs between glaciers, but representatives of cyanobacteria families Pseudanabaenaceae and Phormidiaceae, and algae families Mesotaeniaceae and Ulotrichaceae were the most common. The most of detected cyanobacterial taxa are known to produce polymeric substances (EPS) that may cement granules. Organic matter content in cryoconite varied between glaciers, ranging from 1% to 38%. The geochemistry of all the investigated samples reflected local sediment sources, except of highly concentrated Pb and Hg in cryoconite collected from European glaciers near industrialized regions, corroborating cryoconite as element-specific collector and potential environmental indicator of anthropogenic activity. Our work supports a notion that cryoconite may be more than just simple sediment and instead exhibits complex structure with relevance for biodiversity and the functioning of glacial ecosystems.

Temporal variability of Pu signatures in a 210Pb-dated Sphagnum peat profile from the Northern Ural, Russian Federation.

The peat archives are one of the stratigraphic records revealing clearly physical, chemical and biological signals of human influence on the Earth System since the 1950s, at least. The presented study was aimed mainly to identify the level and origin of anthropogenic radionuclides such as 238, 239, 240Pu in a 210Pb-dated peat profile derived from the Northern Ural, Russian Federation. As stated, the vertical variability of 240Pu/239Pu isotopic compositions reflects the nuclear weapons testing history with the maximum in the 1960s and small regional impact most likely of high-yielded tests in the 1950s as well as Chinese detonations in the 1970s. Peat accumulations rates were similar to those obtained in adjacent areas, whereas 210Pb flux slightly exceeded the reference level established for adequate latitude belt.

Biotope and biocenosis of cryoconite hole ecosystems on Ecology Glacier in the maritime Antarctic.

Despite recent great interest in glacier ecosystems in the continental Antarctic, little is known about their maritime counterparts. Our study presents descriptive data on cryoconite sediments and cryoconite holes on Ecology Glacier (King George Island) to accomplish three main objectives: (a) to identify main eukaryotic (algae, invertebrates) and prokaryotic (cyanobacteria) components of microbial communities; (b) to provide a "baseline" of community composition, organic matter and artificial contamination; and (c) to identify key abiotic factors that might be important in community assembly. Cryoconite holes were sampled along an altitudinal gradient of Ecology Glacier in January, mid Austral Summer 2017. Cryoconite holes located in lower altitude were deeper than those located in the middle and the highest altitude. Seventeen species of algae and cyanobacteria with biomass of 0.79 to 5.37 µg/cm3 have been found in sediments. Dominant species were cyanobacterial Pseudanabaena frigida and Bacillariophyceae Microcostaus sp. Biomass of Bacillariophyceae was significantly higher than that of Chlorophyta and Cyanobacteria. We found three species of rotifers (potentially two new to science) and for the first time a glacier dwelling Acari (suspension feeder, Nanorchestes nivalis). Organic matter content ranged from 5.4% to 7.6%. Investigated artificial radionuclides included 137Cs, 238Pu, 239+240Pu and 241Am. 210Pb seems to be related to organic matter content. Overall, cryoconite holes on Ecology Glacier present unique habitats that serve as biodiversity hotspots of psychrophiles, source of organic matter, matrices for radioactivity tracking and model for observing changes in supraglacial ecosystems in the maritime Antarctic.

Sources and variation of isotopic ratio of airborne radionuclides in Western Arctic lichens and mosses.

This research concerned radioactivity of lichens and mosses from coastal zones of the Canadian Arctic and Alaska. Over 50 samples were collected from 7 positions during two scientific expeditions in 2012 and 2013. The tundra contamination caused by anthropogenic radionuclides was relatively low, reaching mean values with SD's of: 17.4 ±â€¯3.5 Bq/kg for 90Sr, 14.0 ±â€¯2.9 Bq/kg for 134Cs, 38.4 ±â€¯7.5 Bq/kg for 137Cs, 0.86 ±â€¯0.24 Bq/kg for 239+240Pu, 0.065 ±â€¯0.017 Bq/kg for 238Pu and 0.50 ±â€¯0.13 Bq/kg for 241Am. The increase of activity concentration with increasing latitudes was noticed mostly in regard to 90Sr, Pu isotopes and 241Am. The analysis of isotopic ratios exhibited dominant contribution of the global fallout (+SNAP 9A satellite re-entry fallout) for the presence of plutonium isotopes and 241Am. The Fukushima fallout signature was identified in a few lichens from Alaska. However, the influence of additional unknown factor on the occurrence of 90Sr and 137Cs has been detected in western part of Canadian Arctic. Natural radioisotopes of thorium and uranium were found throughout the entire investigated region and the average values of activity concentration with SD's were as follows: 2.92 ±â€¯0.47 Bq/kg for 230Th, 2.61 ±â€¯0.48 Bq/kg for 232Th, 4.32 ±â€¯0.80 Bq/kg for 234U and 3.97 ±â€¯0.71 Bq/kg for 238U. Examined Western Arctic tundra was not affected with any technically enhanced natural radioactivity.

The radioactive contamination study in south-western Greenland tundra in 2012-2013.

The paper presents results of the radioecological investigation carried out in south-western Greenland shoreline. There were examined over 50 samples of lichens and mosses collected from 7 locations during two scientific expeditions conducted in the summer of 2012-2013. The levels, trends and the most likely origin were determined for following natural and artificial radionuclides: 90Sr, 137Cs, 230, 232Th, 234, 238U, 238, 239+240Pu and 241Am. The radioactive pollution was found as relatively low, reaching the maximum values at: 25.3 ± 2.04 Bq/kg for 90Sr, 293 ± 27 Bq/kg for 137Cs, 4.01 ± 0.13 Bq/kg for 239+240Pu, 0.1381 ± 0.0070 Bq/kg for 238Pu and 1.90 ± 0.21 Bq/kg of 241Am, 9.15 ± 0.48 Bq/kg for 230Th, 25.1 ± 1.2 Bq/kg for 232Th, 7.5 ± 1.5 Bq/kg for 234U and 7.26 ± 0.80 Bq/kg for 238U. Both activity and mass isotopic ratio assays revealed dominant contribution of the global fallout + SNAP 9A on the presence of plutonium isotopes and 241Am in Greenland tundra. However, noticeable deviations of 241Am/239+240Pu and to a lesser extend of 240Pu/239Pu ratios from the GF level have been observed. The origin of 137Cs was evidently connected with the coexistence of global and Chernobyl fallout, while the presence of 90Sr was caused by nuclear weapon tests and affected by leaching process. The seaborne signature of uranium isotopes was manifested in research material as well.

The sources of high airborne radioactivity in cryoconite holes from the Caucasus (Georgia).

Cryoconite granules are mixtures of mineral particles, organic substances and organisms on the surface of glaciers where they decrease the ice albedo and are responsible for formation of water-filled holes. The contaminants are effectively trapped in the cryoconite granules and stay there for many years. This study evaluates the contamination level of artificial and natural radionuclides in cryoconite holes from Adishi glacier (Georgia) and identifies the sources of contamination based on activity or mass ratios among artificial radionuclides. Results revealed high activity concentrations of fallout radionuclides reaching 4900 Bq/kg, 2.5 Bq/kg, 107 Bq/kg and 68 Bq/kg for 137Cs, 238Pu, 239+240Pu and 241Am, respectively. The main source of Pu is global fallout, but the low 240Pu/239Pu atomic ratios also indicated local tropospheric source of 239Pu, probably from the Kapustin Yar nuclear test site. Also, high activity ratios of 241Am/239+240Pu could originate from Kapustin Yar. The natural radionuclides originate from the surrounding rocks and were measured to control the environmental processes. 210Pb in cryoconite granules comes predominantly from the atmospheric deposition, and its activity concentrations reach high values up to 12000 Bq/kg.

Airborne radionuclides in the proglacial environment as indicators of sources and transfers of soil material.

A survey of artificial (137Cs, 238Pu, 239+240Pu, 241Am) and natural (226Ra, 232Th, 40K, 210Pb) radioactive isotopes in proglacial soils of an Arctic glacier have revealed high spatial variability of activity concentrations and inventories of the airborne radionuclides. Soil column 137Cs inventories range from below the detection limit to nearly 120 kBq m-2, this value significantly exceeding direct atmospheric deposition. This variability may result from the mixing of materials characterised by different contents of airborne radionuclides. The highest activity concentrations observed in the proglacial soils may result from the deposition of cryoconites, which have been shown to accumulate airborne radionuclides on the surface of glaciers. The role of cryoconites in radionuclide accumulation is supported by the concordant enrichment of the naturally occurring airborne 210Pb in proglacial soil cores showing elevated levels of artificial radionuclides. The lithogenic radionuclides show less variability than the airborne radionuclides because their activity concentrations are controlled only by the mixing of material derived from the weathering of different parent rocks. Soil properties vary little within and between the profiles and there is no unequivocal relationship between them and the radionuclide contents. The inventories reflect the pathways and time variable inputs of soil material to particular sites of the proglacial zone. Lack of the airborne radionuclides reflects no deposition of material exposed to the atmosphere after the 1950s or its removal by erosion. Inventories above the direct atmospheric deposition indicate secondary deposition of radionuclide-bearing material. Very high inventories indicate sites where transport pathways of cryoconite material terminated.

Atmospheric fallout radionuclides in peatland from Southern Poland.

Two peat profiles were collected in a peat bog located in Southern Poland and their geochronology were determined using 210Pb, 238,239+240Pu and 137Cs radiometric techniques. The 210Pb chronologies were established using the constant rate of supply model (CRS) and are in good agreement with the Pu isotopes and 137Cs time markers. Maximum activities of Pu isotopes were found at a depth corresponding to the early 1960s, which is the period characterized by the maximum nuclear weapon tests. The results showed that the 210Pb method is the most accurate technique for the determination age and accumulation rate of a peat. The next part of this study calculated linear accumulation rates by analyzing 238,239+240Pu and 137Cs vertical distributions in the profiles. Activities of fallout isotopes were also measured in plants covering the peatland. The highest activities of 137Cs and 210Pb were found in Calluna vulgaris samples, and 239+240Pu were found only in two samples (C. vulgaris and leaves of Oxycoccus quadripelatus).

Automation of sample processing for ICP-MS determination of 90Sr radionuclide at ppq level for nuclear technology and environmental purposes.

90Sr is a widely determined radionuclide for environmental purposes, nuclear waste control, and can be also monitored in coolants in nuclear reactor plants. In the developed method, the ICP-MS detection was employed together with sample processing in sequential injection analysis (SIA) setup, equipped with a lab-on-valve with mechanized renewal of sorbent bed for solid-phase extraction. The optimized conditions of determination included preconcentration of 90Sr on cation-exchange column and removal of different type of interferences using extraction Sr-resin. The limit of detection of the developed procedure depends essentially on the configuration of the employed ICP-MS spectrometer and on the available volume of the sample to be analyzed. For 1L initial sample volume, the method detection limit (MDL) value was evaluated as 2.9ppq (14.5BqL-1). The developed method was applied to analyze spiked river water samples, water reference materials, and also simulated and real samples of the nuclear reactor coolant.

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.

Accumulation of atmospheric radionuclides and heavy metals in cryoconite holes on an Arctic glacier.

Surface of glaciers is covered by mineral and organic dust, together with microorganisms forming cryoconite granules. Despite fact that glaciers and ice sheets constitute significance part of land surface, reservoir of freshwater, and sites of high biological production, the knowledge on the cryoconite granules still remain unsatisfactory. This study presents information on radionuclide and heavy metal contents in cryoconites. Cryoconites collected from the Hans Glacier in SW Spitsbergen reveal high activity concentrations of anthropogenic ((238,239,240)Pu, (137)Cs, (90)Sr) and natural ((210)Pb) radionuclides. The (238)Pu/(239+240)Pu activity ratios in these cryoconites significantly exceed the mean global fallout ratio (0.025). The (238)Pu/(239+240)Pu ranged from 0.064 to 0.118. The (239+240)Pu/(137)Cs varied from 0.011 ± 0.003 to 0.030 ± 0.007. Such activity ratios as observed in these cryoconites were significantly higher than the values characterizing global fallout, pointing to possible contributions of these radionuclides from other sources. Heavy metals (Pb, Cd, Cu, Zn, Fe, and Mn) in cryoconites exceed both UCC concentrations and local rocks' concentrations, particularly for cadmium. The concentration ratios of stable lead isotopes ((206)Pb/(207)Pb, (208)Pb/(206)Pb) were determined to discriminate between the natural and anthropogenic sources of Pb in cryoconites and to confirm the strong anthropogenic contribution to heavy metal deposition in the Arctic. In investigated cryoconite holes, two groups of invertebrates, both extremophiles, Tardigrada and Rotifera were detected. Our study indicate that cryoconites are aggregates of mineral and organic substances on surfaces of glaciers are able to accumulate large amounts of airborne pollutants bound to extracellular polymeric substances secreted by microorganisms.

Strontium-90 activity concentration in soil samples from the exclusion zone of the Fukushima daiichi nuclear power plant.

The radioactive fission product (90)Sr has a long biological half-life (˜18 y) in the human body. Due to its chemical similarity to calcium it accumulates in bones and irradiates the bone marrow, causing its high radio-toxicity. Assessing (90)Sr is therefore extremely important in case of a nuclear disaster. In this work 16 soil samples were collected from the exclusion zone (<30 km) of the earthquake-damaged Fukushima Daiichi nuclear power plant, to measure (90)Sr activity concentration using liquid scintillation counting. (137)Cs activity concentration was also measured with gamma-spectroscopy in order to investigate correlation with (90)Sr. The (90)Sr activity concentrations ranged from 3.0 ± 0.3 to 23.3 ± 1.5 Bq kg(-1) while the (137)Cs from 0.7 ± 0.1 to 110.8 ± 0.3 kBq kg(-1). The fact that radioactive contamination originated from the Fukushima nuclear accident was obvious due to the presence of (134)Cs. However, (90)Sr contamination was not confirmed in all samples although detectable amounts of (90)Sr can be expected in Japanese soils, as a background, stemming from global fallout due to the atmospheric nuclear weapon tests. Correlation analysis between (90)Sr and (137)Cs activity concentrations provides a potentially powerful tool to discriminate background (90)Sr level from its Fukushima contribution.