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The hydrocarbon seepage chronology during deglaciation across the formerly glaciated Barents Sea was established using uranium-thorium (U–Th) dating of seep carbonates. Seep carbonates were sampled with remotely operated vehicles (ROV) from the seafloor at three active hydrocarbon seeps (water depth 156–383 m), located in the north-west (Storfjordrenna), north-central (Storbanken High), and south-west (Loppa High) Barents Sea. Overall, the U–Th dates range from 13.5 to 1.2 thousand years (ka) before present, indicating episodic seep carbonate formation since the late Pleistocene throughout the Holocene. The new U–Th dates indicate protracted post-glacial gas seepage, congruent with previously published seep carbonate ages from the south-west Barents Sea. Gas hydrate dissociation and associated seep carbonate formation occurred at Storfjordrenna between ≈6 and 1.2 ka, and around 13.5 and 6 ka at Storbanken. Early and late Holocene seep carbonate ages from Loppa High support post-glacial seismic activity as potential seepage trigger mechanism.

We review our current understanding of groundwater flow history in the northern part of the Baltic Artesian Basin (BAB) from the end of the Late Pleistocene to current conditions based on the hydrogeological studies carried out in 2012–2020 by the Department of Geology, Tallinn University of Technology and its partners. Hydrogeochemical data and various numerical models are combined in order to understand the link between glaciations and groundwater flow. The results of our earlier research and published literature on groundwater flow history in the BAB are also taken into account. The reconstruction of groundwater flow history is based on the database of the isotopic, chemical and dissolved gas composition of groundwater. The database contains data on 1155 groundwater samples collected during 1974–2017. We find that groundwater in the BAB is controlled by the mixing of three distinct water masses: interglacial/modern meteoric water (δ18O ≈ –11‰), glacial meltwater (δ18O ≤ –18‰) and an older syngenetic end­member (δ18O ≥–4.5‰). The numerical modelling has suggested that the preservation of meltwater in the northern part of the BAB is controlled by confining layers and the proximity to the outcrop areas of aquifers. Aquifers containing groundwater of glacial origin are in a transient state with respect to modern topographically­driven groundwater flow conditions. The most important topics for future research that can address gaps in our current knowledge are also reviewed.

The effect of freshwater sources on wintertime sea-ice CO2 processes was studied from the glacier front to the outer Tempelfjorden, Svalbard, in sea ice, glacier ice, brine and snow. March–April 2012 was mild, and the fjord was mainly covered with drift ice, in contrast to the observed thicker fast ice in the colder April 2013. This resulted in different physical and chemical properties of the sea ice and under-ice water. Data from stable oxygen isotopic ratios and salinity showed that the sea ice at the glacier front in April 2012 contained on average 54% of frozen-in glacial meltwater. This was five times higher than in April 2013, where the ice was frozen seawater. In April 2012, the largest excess of sea-ice total alkalinity (AT), carbonate ion ([CO32−]) and bicarbonate ion concentrations ([HCO3−]) relative to salinity was mainly related to dissolved dolomite and calcite incorporated during freezing of mineral-enriched glacial water. In April 2013, the excess of these variables was mainly due to ikaite dissolution as a result of sea-ice processes. Dolomite dissolution increased sea-ice AT twice as much as ikaite and calcite dissolution, implying different buffering capacity and potential for ocean CO2 uptake in a changing climate.

Submarine groundwater discharge could impact the transport of critical solutes to the ocean. However, its driver(s), significance over geological time scales, and geographical coverage are poorly understood. We characterize a submarine groundwater seep from the continental slope off northern Norway where substantial amount of meteoric water was detected. We reconstruct the seepage history from textural relationships and U‐Th geochronology of authigenic minerals. We demonstrate how glacial‐interglacial dynamics have promoted submarine groundwater circulation more than 100 km offshore and result in high fluxes of critical solutes to the ocean. Such cryosphere‐hydrosphere coupling is likely common in the circum‐Arctic implying that future decay of glaciers and permafrost in a warming Arctic is expected to attenuate such a coupled process and thus decreases the export of critical solutes.

The geological factors controlling gas release from Arctic deep-water gas reservoirs through seabed methane seeps are poorly constrained. This is partly due to limited data on the precise chronology of past methane emission episodes. Here, we use uranium-thorium dating of seep carbonates sampled from the seabed and from cores drilled at the Vestnesa Ridge, off West Svalbard (79°N, ~1200 m water depth). The carbonate ages reveal three emission episodes during the Penultimate Glacial Maximum (~160,000 to 133,000 years ago), during an interstadial in the last glacial (~50,000 to 40,000 years ago), and in the aftermath of the Last Glacial Maximum (~20,000 to 5,000 years ago), respectively. This chronology suggests that glacial tectonics induced by ice sheet fluctuations on Svalbard mainly controlled methane release from Vestnesa Ridge. Data corroborate past methane release in response to Northern Hemisphere cryosphere variations and suggest that Arctic deep-water gas reservoirs are sensitive to temperature variations over Quaternary time scales.

The late Ludlow Lau Event was a severe biotic crisis in the Silurian, characterized by resurgent microbial facies and faunal turnover rates otherwise only documented during the "big five" mass extinctions. This asynchronous late Silurian marine extinction event preceded an associated positive carbon isotope excursion (CIE), the Lau CIE, although a mechanism for this temporal offset remains poorly constrained. Here, we report thallium isotope data from locally reducing late Ludlow strata within the Baltic Basin to document the earliest onset of global marine deoxygenation. The initial expansion of anoxia coincided with the onset of the extinction and therefore preceded the Lau CIE. Additionally, sulfur isotope data record a large positive excursion parallel to the Lau CIE, interpreted to indicate an increase in pyrite burial associated with the widely documented CIE. This suggests a possible global expansion of euxinia (anoxic and sulfidic water column) following deoxygenation. These data are the most direct proxy evidence of paleoredox conditions linking the known extinction to the Lau CIE through the progressive expansion of anoxia, and most likely euxinia, across portions of the late Silurian oceans.

Major ions were analysed in firn and ice cores located at Fimbul Ice Shelf (FIS), Dronning Maud Land – DML, Antarctica. FIS is the largest ice shelf in the Haakon VII Sea, with an extent of approximately 36 500 km2. Three shallow firn cores (about 20 m deep) were retrieved in different ice rises, Kupol Ciolkovskogo (KC), Kupol Moskovskij (KM), and Blåskimen Island (BI), while a 100 m long core (S100) was drilled near the FIS edge. These sites are distributed over the entire FIS area so that they provide a variety of elevation (50–400 m a.s.l.) and distance (3–42 km) to the sea. Sea-salt species (mainly Na+ and Cl−) generally dominate the precipitation chemistry in the study region. We associate a significant sixfold increase in median sea-salt concentrations, observed in the S100 core after the 1950s, to an enhanced exposure of the S100 site to primary sea-salt aerosol due to a shorter distance from the S100 site to the ice front, and to enhanced sea-salt aerosol production from blowing salty snow over sea ice, most likely related to the calving of Trolltunga occurred during the 1960s. This increase in sea-salt concentrations is synchronous with a shift in non-sea-salt sulfate (nssSO42−) toward negative values, suggesting a possible contribution of fractionated aerosol to the sea-salt load in the S100 core most likely originating from salty snow found on sea ice. In contrast, there is no evidence of a significant contribution of fractionated sea salt to the ice-rises sites, where the signal would be most likely masked by the large inputs of biogenic sulfate estimated for these sites. In summary, these results suggest that the S100 core contains a sea-salt record dominated by the proximity of the site to the ocean, and processes of sea ice formation in the neighbouring waters. In contrast, the ice-rises firn cores register a larger-scale signal of atmospheric flow conditions and a less efficient transport of sea-salt aerosols to these sites. These findings are a cont

The climate impact of black carbon (BC) is notably amplified in the Arctic by its deposition, which causes albedo decrease and subsequent earlier snow and ice spring melt. To comprehensively assess the climate impact of BC in the Arctic, information on both atmospheric BC concentrations and deposition is essential. Currently, Arctic BC deposition data are very scarce, while atmospheric BC concentrations have been shown to generally decrease since the 1990s. However, a 300-year Svalbard ice core showed a distinct increase in EC (elemental carbon, proxy for BC) deposition from 1970 to 2004 contradicting atmospheric measurements and modelling studies. Here, our objective was to decipher whether this increase has continued in the 21st century and to investigate the drivers of the observed EC deposition trends. For this, a shallow firn core was collected from the same Svalbard glacier, and a regional-to-meso-scale chemical transport model (SILAM) was run from 1980 to 2015. The ice and firn core data indicate peaking EC deposition values at the end of the 1990s and lower values thereafter. The modelled BC deposition results generally support the observed glacier EC variations. However, the ice and firn core results clearly deviate from both measured and modelled atmospheric BC concentration trends, and the modelled BC deposition trend shows variations seemingly independent from BC emission or atmospheric BC concentration trends. wet-deposited at this Svalbard glacier, indicating that meteorological processes such as precipitation and scavenging efficiency have most likely a stronger influence on the BC deposition trend than BC emission or atmospheric concentration trends. BC emission source sectors contribute differently to the modelled atmospheric BC concentrations and BC deposition, which further supports our conclusion that different processes affect atmospheric BC concentration and deposition trends. Consequently, Arctic BC deposition trends should not directly be inf