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Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species
Treated effluent discharge from uranium (U) mines and mills elevates the concentrations of U, calcium (Ca), magnesium (Mg), and sulfate (SO(4)(2–)) above natural levels in receiving waters. Many investigations on the effect of hardness on U toxicity have been experiments on the combined effects of c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365698/ https://www.ncbi.nlm.nih.gov/pubmed/25475484 http://dx.doi.org/10.1002/etc.2834 |
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author | Goulet, Richard R Thompson, Patsy A Serben, Kerrie C Eickhoff, Curtis V |
author_facet | Goulet, Richard R Thompson, Patsy A Serben, Kerrie C Eickhoff, Curtis V |
author_sort | Goulet, Richard R |
collection | PubMed |
description | Treated effluent discharge from uranium (U) mines and mills elevates the concentrations of U, calcium (Ca), magnesium (Mg), and sulfate (SO(4)(2–)) above natural levels in receiving waters. Many investigations on the effect of hardness on U toxicity have been experiments on the combined effects of changes in hardness, pH, and alkalinity, which do not represent water chemistry downstream of U mines and mills. Therefore, more toxicity studies with water chemistry encountered downstream of U mines and mills are necessary to support predictive assessments of impacts of U discharge to the environment. Acute and chronic U toxicity laboratory bioassays were realized with 6 freshwater species in waters of low alkalinity, circumneutral pH, and a range of chemical hardness as found in field samples collected downstream of U mines and mills. In laboratory-tested waters, speciation calculations suggested that free uranyl ion concentrations remained constant despite increasing chemical hardness. When hardness increased while pH remained circumneutral and alkalinity low, U toxicity decreased only to Hyalella azteca and Pseudokirchneriella subcapitata. Also, Ca and Mg did not compete with U for the same uptake sites. The present study confirms that the majority of studies concluding that hardness affected U toxicity were in fact studies in which alkalinity and pH were the stronger influence. The results thus confirm that studies predicting impacts of U downstream of mines and mills should not consider chemical hardness. |
format | Online Article Text |
id | pubmed-4365698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43656982015-03-23 Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species Goulet, Richard R Thompson, Patsy A Serben, Kerrie C Eickhoff, Curtis V Environ Toxicol Chem Environmental Toxicology Treated effluent discharge from uranium (U) mines and mills elevates the concentrations of U, calcium (Ca), magnesium (Mg), and sulfate (SO(4)(2–)) above natural levels in receiving waters. Many investigations on the effect of hardness on U toxicity have been experiments on the combined effects of changes in hardness, pH, and alkalinity, which do not represent water chemistry downstream of U mines and mills. Therefore, more toxicity studies with water chemistry encountered downstream of U mines and mills are necessary to support predictive assessments of impacts of U discharge to the environment. Acute and chronic U toxicity laboratory bioassays were realized with 6 freshwater species in waters of low alkalinity, circumneutral pH, and a range of chemical hardness as found in field samples collected downstream of U mines and mills. In laboratory-tested waters, speciation calculations suggested that free uranyl ion concentrations remained constant despite increasing chemical hardness. When hardness increased while pH remained circumneutral and alkalinity low, U toxicity decreased only to Hyalella azteca and Pseudokirchneriella subcapitata. Also, Ca and Mg did not compete with U for the same uptake sites. The present study confirms that the majority of studies concluding that hardness affected U toxicity were in fact studies in which alkalinity and pH were the stronger influence. The results thus confirm that studies predicting impacts of U downstream of mines and mills should not consider chemical hardness. BlackWell Publishing Ltd 2015-03 2015-02-10 /pmc/articles/PMC4365698/ /pubmed/25475484 http://dx.doi.org/10.1002/etc.2834 Text en © 2014 The Authors. Published by Wiley Periodicals, Inc. on behalf of SETAC http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Environmental Toxicology Goulet, Richard R Thompson, Patsy A Serben, Kerrie C Eickhoff, Curtis V Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species |
title | Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species |
title_full | Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species |
title_fullStr | Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species |
title_full_unstemmed | Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species |
title_short | Impact of Environmentally Based Chemical Hardness on Uranium Speciation and Toxicity in Six Aquatic Species |
title_sort | impact of environmentally based chemical hardness on uranium speciation and toxicity in six aquatic species |
topic | Environmental Toxicology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365698/ https://www.ncbi.nlm.nih.gov/pubmed/25475484 http://dx.doi.org/10.1002/etc.2834 |
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