Baltic Sea water tritium and stable isotopes in 2016-2017.

Water samples from the different basins of the Baltic Sea and North Sea were collected during four cruises taken place in 2016-2017. Altogether 60 water samples for 3H activity concentration and 120 water samples for stable isotopes ratio (δ18O and δ2H) were analysed. Exceptionally strong inflow activity from North Sea to the Baltic Sea occurred prior our surveys. The data obtained enabled comprehensive evaluation of tritium and stable isotopes distribution in waters of Baltic Sea and contributing inputs, including riverine and atmospheric freshwater flux and saline water inflow through the Danish Straits. By comparing with the previous studies, we noticed a tendency toward an increase in the δ18O and δ2H values of zero-salinity component over time, which may be due to climate change. In the case of tritium, the influence of artificial sources has also been noticed.

A 160,000-year-old history of tectonically controlled methane seepage in the Arctic.

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.

Free amino acids in the Arctic snow and ice core samples: Potential markers for paleoclimatic studies.

The role of oceanic primary production on climate variability has long been debated. Defining changes in past oceanic primary production can help understanding of the important role that marine algae have in climate variability. In ice core research methanesulfonic acid is the chemical marker commonly used for assessing changes in past primary production. However, other organic compounds such as amino acids, can be produced and emitted into the atmosphere during a phytoplankton bloom. These species can be transported and deposited onto the ice cap in polar regions. Here we investigate the correlation between the concentration of chlorophyll-a, marker of marine primary production, and amino acids present in an ice core. For the first time, free l- and d-amino acids in Arctic snow and firn samples were determined by a sensitive and selective analytical method based on liquid chromatography coupled with tandem mass spectrometry. The new method for the determination of free amino acids concentrations was applied to firn core samples collected on April 2015 from the summit of the Holtedahlfonna glacier, Svalbard (N 79'08.424, E 13'23.639, 1120m a.s.l.). The main results of this work are summarized as follows: (1) glycine, alanine and proline, were detected and quantified in the firn core samples; (2) their concentration profiles, compared with that of the stable isotope δ18O ratio, show a seasonal cycling with the highest concentrations during the spring and summer time; (3) back-trajectories and Greenland Sea chlorophyll-a concentrations obtained by satellite measurements were compared with the amino acids profile obtained from ice core samples, this provided further insights into the present results. This study suggests that the amino acid concentrations in the ice samples collected from the Holtedahlfonna glaciers could reflect changes in oceanic phytoplankton abundance.

Investigations of the unsaturated zone at two radioactive waste disposal sites in Lithuania.

The unsaturated zone is an important part of the water cycle, governed by many hydrological and hydrogeological factors and processes and provide water and nutrients to the terrestrial ecosystem. Besides, the soils of the unsaturated zone are regarded as the first natural barrier to a large extent and are able to limit the spread of contaminants depending on their properties. The unsaturated zone provides a linkage between atmospheric moisture, groundwater, and seepage of groundwater to streams, lakes, or other surface water bodies. The major difference between water flow in saturated and unsaturated soils is that the hydraulic conductivity, which is conventionally assumed to be a constant in saturated soils, is a function of the degree of saturation or matrix suction in the unsaturated soils. In Lithuania, low and intermediate level radioactive wastes generated from medicine, industry and research were accumulated at the Maisiagala radioactive waste repository. Short-lived low and intermediate levels radioactive waste, generated during the operation of the Ignalina Nuclear Power Plant (INPP) and arising after the INPP decommissioning will be disposed of in the near surface repository close to the INPP (Stabatiske site). Extensive data sets of the hydraulic properties and water content attributed to unsaturated zone soil profiles of the two radioactive waste disposal sites have been collected and summarized. Globally widespread radionuclide tritium ((3)H) and stable isotope ratio ((18)O/(16)O and (2)H/(1)H) distribution features were determined in precipitation, unsaturated zone soil moisture profiles and groundwater.

Pleistocene age paleo-groundwater inferred from water-stable isotope values in the central part of the Baltic Artesian Basin.

A new data set of δ(2)H and δ(18)O in the groundwater from the central part of the Baltic Artesian Basin is presented. The hydrogeological section is subdivided into stagnation, slow exchange and active exchange zones. Na-Ca-Cl brine found at the deepest part - the stagnation zone - is characterized by δ(18)O values above -5 ‰ and δ(2)H values approaching -40 ‰ with respect to Vienna Standard Mean Ocean Water. The slow exchange zone where waters of mostly intermediate salinity reside is characterized by δ(18)O values around -11.7 ‰ and δ(2)H values around -85.3 ‰. Mean δ(18)O and δ(2)H values of the fresh groundwater in the active water exchange zone are -11.1 and -79.9 ‰, respectively. Characteristically, the groundwater in the active and slow exchange zone is isotopically more depleted compared with the precipitation values observed, and the depletion increases with depth down to the level where strongly enriched brines are encountered.

Role of a productive lake in carbon sequestration within a calcareous catchment.

For a long time, lakes were considered unimportant in the global carbon (C) cycle because of their small total area compared to the ocean. Over the last two decades, a number of studies have highlighted the important role of lakes in both sequestering atmospheric C and modifying the C flux from the catchment by degassing CO2 and methane and burying calcite and organic matter in the sediment. Based on a full C mass balance, high frequency measurements of lake metabolism and stable isotope analysis of a large shallow eutrophic lake in Estonia, we assess the role alkaline lakes play in augmenting the strength of terrestrial carbonate weathering as a temporary CO2 sink. We show that a large part of organic C buried in the sediments in this type of lakes originates from the catchment although a direct uptake from the atmosphere during periods of intensive phytoplankton growth in eutrophic conditions contributes to the carbon sink.

Timescales of methane seepage on the Norwegian margin following collapse of the Scandinavian Ice Sheet.

Gas hydrates stored on continental shelves are susceptible to dissociation triggered by environmental changes. Knowledge of the timescales of gas hydrate dissociation and subsequent methane release are critical in understanding the impact of marine gas hydrates on the ocean-atmosphere system. Here we report a methane efflux chronology from five sites, at depths of 220-400 m, in the southwest Barents and Norwegian seas where grounded ice sheets led to thickening of the gas hydrate stability zone during the last glaciation. The onset of methane release was coincident with deglaciation-induced pressure release and thinning of the hydrate stability zone. Methane efflux continued for 7-10 kyr, tracking hydrate stability changes controlled by relative sea-level rise, bottom water warming and fluid pathway evolution in response to changing stress fields. The protracted nature of seafloor methane emissions probably attenuated the impact of hydrate dissociation on the climate system.