The origin of Uranium in groundwater of the eastern Halkidiki region, northern Greece.

Uranium (U) pollution in groundwater has become a serious problem worldwide. Even in low concentrations, U has both radiological and toxicological impacts on human health. In this study an integrated hydrogeological approach was applied to conceptualize an aquifer system, and determine the origin of U detected in the aquifer of the eastern Halkidiki region in northern Greece. Data from measurements of groundwater level and hydrochemical and stable isotope analyses of groundwater samples were applied to perform geochemical modeling and multivariate statistical analysis. The modeling and statistical analysis identified three hydrogeochemical groups within the studied hydro-system, and U(VI) as the dominant U species. The first group is linked to the deeper aquifer which is characterized by water-rock interactions with weathering products of granodiorite. In this group the dominant U species is uranyl phosphate and U concentration is 3.7 µg/L. The upper aquifer corresponds to the second hydrogeochemical group where U concentrations are mainly influenced by high concentrations of nitrogen species (NO3- and NO2-). Factor analysis further discriminated the upper aquifer into a saline coastal zone and an inland zone impacted by agricultural activities. The third hydrogeochemical group presents the highest concentration of U (up to 15 µg/L) in groundwater and corresponds to the internal aquifer system. The U within this system is triggered by the presence of Mn2+, while the long residence time of the groundwater contributes synergistically to the hydrogeochemical process. Manganese triggers U oxidation in parallel with Fe2+ precipitation that acts as a regulator of U concentration. Groundwater depletion of the upper aquifers promotes the up-coning of geothermal fluids from fault zones leading to increased concentrations of U in the mid-depth aquifers.

Origin, implications and management strategies for nitrate pollution in surface and ground waters of Anthemountas basin based on a δ15N-NO3- and δ18O-NO3- isotope approach.

Nitrate pollution of surface and groundwater resources is a major worldwide environmental problem. In this study nitrogen isotopes of water, soil, fertilizer and manure were analyzed to determine the pollution sources of nitrate in the groundwater and surface waters of Anthemountas basin. The SIAR model and multivariate statistical analysis were used to determine and quantify the contribution of different NO3̄ sources in groundwater and surface water. Additionally, a detailed literature overview was carried out to identify the origin of nitrate pollution in surface and ground waters based on ΝΟ3- isotopes. The Piper diagram identified the dominant water types as Mg-Ca-HCO3 and Ca-Mg-HCO3. Nitrate concentrations reached 162.0 mg/L in groundwater and 39.0 mg/L in surface waters. The main source of nitrate in groundwater was mainly nitrified ammonium-based synthetic urea and less nitrate-based synthetic fertilizers. The correlation of SIAR results with other trace elements revealed a negative correlation between hexavalent chromium and a) nitrate-based synthetic fertilizers, and b) nitrification of urea synthetic fertilizers. However, a positive correlation was observed between hexavalent chromium and anthropogenic organic matter. The literature overview provided the basis to design a novel management protocol for nitrate pollution that includes three steps: a) fundamental research, b) management tools, c) monitoring and preservation actions. However, an integrated management protocol for nitrate pollution requires a deeper understanding of the hydro-system and the full participation of local farmers and stakeholders.