Polonium-210 accumulates in a lake receiving coal mine discharges—anthropogenic or natural?
Creators
- 1. Department of Chemistry, University of Iowa, Chemistry Building, 251 North Capitol Street, Iowa City, IA 52242 (United States)
- 2. University of Iowa State Hygienic Laboratory, Research Park, State Hygienic Laboratory 2490, Crosspark Road, Coralville, IA 52242 (United States)
- 3. Interdisciplinary Human Toxicology Program, University of Iowa, Iowa City, IA 52242 (United States)
- 4. Department of Environmental and Occupational Health, College of Public Health, University of Iowa, 145 N. Riverside Drive, 100 CPHB, Iowa City, IA 52242 (United States)
- 5. Departments of Radiology and Radiation Oncology, Free Radical and Radiation Biology Program, University of Iowa, ML B180 FRRB, 500 Newton Road, Iowa City, IA 52242 (United States)
Description
Coal is an integral part of global energy production; however, coal mining is associated with numerous environmental health impacts. It is well documented that coal-mine waste can contaminate the environment with naturally-occurring radionuclides from the uranium-238 (238U) decay series. However, the behavior of the final radionuclide in the 238U-series, i.e., polonium-210 (210Po) arising from coal-mine waste-water discharge is largely unexplored. Here, results of a year-long (2014–2015) field study, in which the concentrations of 210Po in sediments and surface water of a lake that receives coal-mine waste-water discharge in West Virginia are presented. Initial measurements identified levels of 210Po in the lake sediments that were in excess of that which could be attributed to ambient U-series parent radionuclides; and were indicative of discharge site contamination of the lake ecosystem. However, control sediment obtained from a similar lake system in Iowa (an area with no coal mining or unconventional drilling) suggests that the levels of 210Po in the lake are a natural phenomenon; and are likely unrelated to waste-water treatment discharges. Elevated levels of 210Po have been reported in lake bottom sediments previously, yet very little information is available on the radioecological implications of 210Po accumulation in lake bottom sediments. The findings of this study suggest that (Monthly Energy Review, 2016) the natural accumulation and retention of 210Po in lake sediments may be a greater than previously considered (Chadwick et al., 2013) careful selection of control sites is important to prevent the inappropriate attribution of elevated levels of NORM in lake bottom ecosystems to industrial sources; and (Van Hook, 1979) further investigation of the source-terms and potential impacts on elevated 210Po in lake-sediment ecosystems is warranted. - Highlights: • 210Po accumulates in lake bottom sediments downstream of water treatment facility. • 210Po approximately 10-fold higher than parent 238U. • Increased levels of 210Po appear to be a natural phenomenon. • More studies are needed to understand the bioaccumulation pathways of 210Po.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jenvrad.2016.10.023Additional details
Identifiers
- DOI
- 10.1016/j.jenvrad.2016.10.023;
- PII
- S0265-931X(16)30391-5;
Publishing Information
- Journal Title
- Journal of Environmental Radioactivity
- Journal Volume
- 167
- Journal Page Range
- p. 211-221
- ISSN
- 0265-931X
- CODEN
- JERAEE
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49056121
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- BIOLOGICAL ACCUMULATION; BUILDUP; COAL MINES; COAL MINING; ECOSYSTEMS; ENVIRONMENTAL IMPACTS; IOWA; LAKES; LEAD 210; POLONIUM 210; SEDIMENTS; SOURCE TERMS; URANIUM 238; WASTE WATER; WATER TREATMENT; WEST VIRGINIA
- Descriptors DEC
- ACTINIDE NUCLEI; ALPHA DECAY RADIOISOTOPES; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; DAYS LIVING RADIOISOTOPES; DEVELOPED COUNTRIES; EVEN-EVEN NUCLEI; HEAVY NUCLEI; HYDROGEN COMPOUNDS; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LEAD ISOTOPES; LIQUID WASTES; MINES; MINING; NANOSECONDS LIVING RADIOISOTOPES; NORTH AMERICA; NUCLEI; OXYGEN COMPOUNDS; POLONIUM ISOTOPES; RADIOISOTOPES; SPONTANEOUS FISSION RADIOISOTOPES; SURFACE WATERS; UNDERGROUND FACILITIES; URANIUM ISOTOPES; USA; WASTES; WATER; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.