Hydrochemical and geological controls on dissolved radium and radon in northwestern Algeria hydrothermal groundwaters.

This study presents the results of the first investigation on natural occurrence of radium and radon in Algerian thermal water systems. Activity concentrations of Rn and Ra isotopes were measured in sixteen hydrothermal springs of northwestern Algeria. Samples displayed high activities, especially for 222Rn, 224Ra and 226Ra (up to 377 × 103 Bq/m3, 730 Bq/m3 and 4470 Bq/m3, respectively). Approximately, 50% of the investigated springs displayed activities of combined long-lived Ra (226Ra + 228Ra) in excess of the maximum contaminant level (MCL) of the WHO and EPA for drinking water. Factors controlling the distribution of radionuclides in the aquifer system are investigated. The observed correlation between Ra isotope and TDS suggests that adsorption/desorption is not the dominant process controlling the distribution of Ra in waters. Our results indicate that the excess SO42- limits the concentration of dissolved Ba2+ and thereby, the elevated Ra activities in these hydrothermal systems are not simply limited by co-precipitation with BaSO4 (barite). The data shows that Ra activities are likely dominated by the recoil process of parent isotopes in the aquifer solids. The minimal abundance of clay minerals and oxides in the aquifer, in addition to thermal activities in northwestern Algeria, significantly enhances the mobilization of Ra into waters.

Tritium in river waters from French Mediterranean catchments: Background levels and variability.

Tritium background levels in various environmental compartments are deeply needed in particular to assess radiological impact, especially in river systems where most of releases from nuclear facilities are performed. The present study aims to identify the main environmental factors that influence tritium background levels in rivers at the regional scale. 41 samples were collected from 2014 to 2016 along 17 small rivers in the south of France. All were located out of the influence of direct releases from nuclear facilities. Tritiated water (HTO) concentrations measured in water samples ranged from 0.12±0.11 to 0.86±0.15BqL-1 and HTO concentrations in rains were modelled between 2015 and 2016 over the study period referring to time series acquired from 1963 to 2014 at Thonon-les-Bains monitoring station. The results of tritium concentrations in rivers studied present a significant variability and are more than twice lower than forecasted values in rain. Multiple linear regressions allowed identifying that HTO concentration in rains, watershed area and altitude were the main tested parameters that are linked to the variability of HTO concentrations in the studied rivers. Finally, HTO fluxes delivered to the Mediterranean Sea by French coastal rivers out of influence of nuclear releases were estimated. The results highlight that those account for around 1% of HTO exported while 99% are transferred by the nuclearized Rhone River.