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.

Distribution, composition and risk assessment of PAHs and PCBs in cryospheric watersheds of the eastern Tibetan Plateau.

Polycyclic Aromatic Hydrocarbons (PAHs) and Polychlorinated Biphenyls (PCBs) are significant components of persistent organic pollutants (POPs) and pose a threat to both ecosystems and human health. To explore their spatial distribution, origins, and risk assessment, we collected 25 glacial meltwater and downstream river water samples in the eastern Tibetan Plateau (including the Qilian Mountains in the northeast) during the summer of 2022 (June-July). Our results showed that ∑PAHs and ∑PCBs were present in a wide range from ND-1380 ng/L and ND-1421 ng/L, respectively. Compared to other studies worldwide, the ∑PAHs and ∑PCBs in the Hengduan Mountains were at high levels. The PAHs and PCBs mainly consisted of low-molecular-weight homologs, including Ace, Flu, Phe, and PCB52. Phe was the primary component of PAHs. Glacial meltwater samples generally exhibited low concentration of PAHs and PCB52, whereas downstream river water samples typically showed high concentration of PAHs and PCB52. We attributed this characteristic to the influence of pollutants physicochemical properties, altitude effect, long-range transport (LRT), and local environmental conditions. In the eastern Tibetan Plateau glacier basin (especially in the Hailuogou watersheds), the concentration of PAHs and PCB52 in runoff generally increased with decreasing elevation. We believe that the primary factor affecting the concentration of PAHs and PCB52 in the region is the difference in local human activity inputs from various altitudes. The composition characteristics of PAHs and PCBs suggested that incomplete coal combustion and coking discharge mainly caused PAHs, while the combustion of coal and charcoal and the release of capacitors primarily caused PCBs. We assessed the carcinogenic risk of PAHs and PCBs in the glacier basin of the TP and found that the potential threat of PAHs was stronger than that of PCBs. Overall, this study provides new insights into the ecological security of water resources in eastern Tibetan Plateau. It is significant for controlling PAHs and PCBs emissions, assessing the ecological environment of the glacier watershed, and regional human health.

Insights on the distribution and environmental implications of the radio-isotope 235U in surface soils and glaciers of the Tibetan Plateau.

Atom ratio between 235U and 238U is often used as an indicator of U contamination as the isotopic signature of products generated by the nuclear and military industry significantly vary from the natural isotopic ratio of U. In this study, surface soils and glaciers samples were collected in the Tibetan Plateau (TP) and its surrounding areas and analyzed for U isotopic composition. Results show that the 235U/238U atom ratios in the surface soils of the TP ranges from 0.007122 to 0.007615, with an average value of 0.007378 ± 0.00011; while in the snow/ice dust from high-altitude glaciers it ranges from 0.007254 to 0.007687, with an average value of 0.007345 ± 0.000128. These ratios are slightly higher than the typical crustal value, indicating that the TP was affected by an anthropogenic input of 235U, especially in its northeast and southwest sectors. The variability of our results suggests that the spatial distribution of this contamination is not uniform, pointing to differences in the potential sources and transmission paths of radioactive particles. Combining the knowledge of past tests and activities conducted in the geographic areas around the TP with the knowledge of prevailing winds, we hypothesize that the observed 235U contamination in the TP surface soils and glaciers may have originated mainly from the previous nuclear related activities in surrounding areas (e.g., north Gobi Desert and South Asia). In addition, the horizontal and vertical wind field around the Tibetan Plateau, as well as the atmospheric aerosol optical thickness data also demonstrated the possible transport paths of the radionuclides, that is, originated from in northern Gobi desert and South Asia and reached the TP crossing the Himalayas.

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.

Jarosite formation in deep Antarctic ice provides a window into acidic, water-limited weathering on Mars.

Many interpretations have been proposed to explain the presence of jarosite within Martian surficial sediments, including the possibility that it precipitated within paleo-ice deposits owing to englacial weathering of dust. However, until now a similar geochemical process was not observed on Earth nor in other planetary settings. We report a multi-analytical indication of jarosite formation within deep ice. Below 1000 m depth, jarosite crystals adhering on residual silica-rich particles have been identified in the Talos Dome ice core (East Antarctica) and interpreted as products of weathering involving aeolian dust and acidic atmospheric aerosols. The progressive increase of ice metamorphism and re-crystallization with depth, favours the relocation and concentration of dust and the formation of acidic brines in isolated environments, allowing chemical reactions and mineral neo-formation to occur. This is the first described englacial diagenetic mechanism occurring in deep Antarctic ice and supports the ice-weathering model for jarosite formation on Mars, highlighting the geologic importance of paleo ice-related processes on this planet. Additional implications concern the preservation of dust-related signals in deep ice cores with respect to paleoclimatic reconstructions and the englacial history of meteorites from Antarctic blue ice fields.

East Greenland ice core dust record reveals timing of Greenland ice sheet advance and retreat.

Accurate estimates of the past extent of the Greenland ice sheet provide critical constraints for ice sheet models used to determine Greenland's response to climate forcing and contribution to global sea level. Here we use a continuous ice core dust record from the Renland ice cap on the east coast of Greenland to constrain the timing of changes to the ice sheet margin and relative sea level over the last glacial cycle. During the Holocene and the previous interglacial period (Eemian) the dust record was dominated by coarse particles consistent with rock samples from central East Greenland. From the coarse particle concentration record we infer the East Greenland ice sheet margin advanced from 113.4 ± 0.4 to 111.0 ± 0.4 ka BP during the glacial onset and retreated from 12.1 ± 0.1 to 9.0 ± 0.1 ka BP during the last deglaciation. These findings constrain the possible response of the Greenland ice sheet to climate forcings.

137Cs contamination in the Adamello glacier: Improving the analytical method.

An alpine ice core, extracted from the Adamello glacier (Central Italian Alps), was analyzed in its entire length through low background γ-spectroscopy, for the detection of 137Cs. Our results show that in glacier ice 137Cs is tightly bound to insoluble particulate matter inside the ice core, and it is therefore possible to restrict γ-spectroscopy analysis to particulate matter only. We show how the sensibility of the detection limit can be improved by almost one order of magnitude by using a well-type detector instead of a coaxial one. Hypothesis on the dating of some radioactive layers are also hereby presented.

Author Correction: Cryoconite as a temporary sink for anthropogenic species stored in glaciers.

A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has not been fixed in the paper.

Cryoconite as a temporary sink for anthropogenic species stored in glaciers.

Cryoconite, the typical sediment found on the surface of glaciers, is mainly known in relation to its role in glacial microbiology and in altering the glacier albedo. But if these aspects are relatively well addressed, the same cannot be said about the geochemical properties of cryoconite and the possible interactions with glacial and peri-glacial environment. Current glacier retreat is responsible for the secondary emission of species deposited in high-altitude regions in the last decades. The role played by cryoconite in relation to such novel geochemical fluxes is largely unknown. Few and scarce observations suggest that it could interact with these processes, accumulating specific substances, but why, how and to what extent remain open questions. Through a multi-disciplinary approach we tried to shed lights. Results reveal that the peculiar composition of cryoconite is responsible for an extreme accumulation capability of this sediment, in particular for some, specific, anthropogenic substances.

A new method based on low background instrumental neutron activation analysis for major, trace and ultra-trace element determination in atmospheric mineral dust from polar ice cores.

Dust found in polar ice core samples present extremely low concentrations, in addition the availability of such samples is usually strictly limited. For these reasons the chemical and physical analysis of polar ice cores is an analytical challenge. In this work a new method based on low background instrumental neutron activation analysis (LB-INAA) for the multi-elemental characterization of the insoluble fraction of dust from polar ice cores is presented. Thanks to an accurate selection of the most proper materials and procedures it was possible to reach unprecedented analytical performances, suitable for ice core analyses. The method was applied to Antarctic ice core samples. Five samples of atmospheric dust (µg size) from ice sections of the Antarctic Talos Dome ice core were prepared and analyzed. A set of 37 elements was quantified, spanning from all the major elements (Na, Mg, Al, Si, K, Ca, Ti, Mn and Fe) to trace ones, including 10 (La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb and Lu) of the 14 natural occurring lanthanides. The detection limits are in the range of 10(-13)-10(-6) g, improving previous results of 1-3 orders of magnitude depending on the element; uncertainties lies between 4% and 60%.