Toxicity of tailing leachates from a niobium mine toward three aquatic organisms.

The aim of this research was to assess the ecotoxicity of leachates originating from a niobium mine located in Canada. These tailings contain considerable amounts of carbonates and phosphates and could potentially be used as fertilizer for agriculture. However, the presence of different contaminants linked with the ores mined, including rare earth elements and daughter elements of the uranium disintegration chain is of concern. Bioassays have been used to determine if the tailings leachates could be harmful. The assessment of the toxicity of progressive dilutions of five tailing leachates (808, 809, 810, 811 and 897) was performed on different organisms: phytoplankton Raphidocelis subcapitata and duckweed Lemna minor, based on their growth and chlorophyll a content, and water flea Daphnia magna based on their mobility, mortality and reproduction. Overall, the leachates showed higher toxicity to Raphidocelis subcapitata and Lemna minor, than toward Daphnia magna. Leachate 808 showed no toxicity to all organisms while leachate 810 showed significant effects to all species. The results can be explained by the leachate dissolved metal or nutrient concentrations, but also by the metal bioavailability which depends on pH and hardness. Generally, toxicity was observed in undiluted samples tested, which is not representative of the conditions that could occur in the environment. This supports the idea that these tailings could be used as fertilizer albeit more studies may be required, particularly to assess the toxicity of the tailings leachate for benthic organisms, the toxicity of the tailings for terrestrial organisms and the variations of soil and sediment physicochemical properties after tailing treatments.

A rapid sequential chromatographic separation of U- and Th-decay series radionuclides in water samples.

A new sequential protocol for the separation and preconcentration of U, Th, Ra, Po and Pb for the same sample aliquot has been designed. The optimized stacking of chromatographic resins [TRU, Sr and a new hybrid Ra resin (composed of Analig Ra-01 and cation exchange AG50Wx8)] enables a rapid loading of the sample (less than 75 min for 300 mL of samples) while ensuring a high retention of the analytes of interest. The use of a hybrid Ra resin allows the complete and selective extraction of Ra on a solid support, a feature lacking in other sequential separation procedures. A loading medium composed of 1 M HNO3 and chloride ions (as NH4Cl) was found suitable for the retention of all analytes of interest onto the stacked chromatographic resins. The proposed elution conditions facilitate the complete segregation of individual elements in 5 distinctive fractions, reducing the risk of spectral and non-spectral interferences. This feature enables the proper quantification of the radioisotopes either by ICP-MS or alpha spectrometry below national and international regulatory guidelines. The mean chemical recoveries for the separation are 93, 98, 105, 88, and 98% for U, Th, Ra, Po and Pb, respectively. Reproducible yields were obtained independently of the water type tested, demonstrating the versatility and the robustness of the proposed methodology.