Title | Uranium mobility in groundwater at historical mine sites in the Bancroft region of Ontario, Canada |
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Author | Desbarats, A J ;
Percival, J B ; Venance, K E |
Source | GSA Annual Meeting in Seattle, Washington, USA - 2017; Geological Society of America, Abstracts With Programs vol. 49, no. 6, 299-7, 2017 p. 1, https://doi.org/10.1130/abs/2017AM-299517 |
Links | Online - En ligne
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Year | 2017 |
Alt Series | Natural Resources Canada, Contribution Series 20170185 |
Publisher | Geological Society of America |
Meeting | Geological Society of America, Annual Meeting; Seattle, WA; US; October 22-25, 2017 |
Document | serial |
Lang. | English |
Media | on-line; digital |
File format | html; pdf (Adobe® Reader®) |
Program | Environmental Geoscience Tools for environmental impacts and adaptation for metal mining |
Released | 2017 10 01 |
Abstract | Granitic pegmatite-hosted U-Th-REE deposits are widespread within the Grenville geological province of eastern Canada. Around Bancroft, Ontario, during a uranium exploration boom in the 1950s, four of
these deposits entered production while numerous others saw underground development. The environmental legacy of past mining and renewed exploration activities in the area have raised public concerns about potential impacts to groundwater quality. To
investigate these concerns, groundwater at ten historical mine properties was sampled in drill holes, flowing adits and flooded shafts. Uranium occurs almost entirely in the dissolved (< 0.45micrometre) phase at concentrations varying between 0.6 and
2579 microgram/L. The Canadian standard for U in drinking water (20 microgram/L) is exceeded in 70% of samples. By comparison, background concentrations in nearby un-mineralized granitic Precambrian bedrock range between 0.02 and 66 microgram/L and
only 5% of values exceed the standard. The mineralogy and solubility of U-bearing minerals are important primary controls on U concentrations. While uraninite and uranothorite are the main U-bearing phases, uranothorite may be more soluble because of
its non-ideal composition and metamict structure. The highest U concentrations are observed in shallow, oxic groundwaters and speciation modeling indicates that over 98% of dissolved U is in the form of highly mobile uranyl-Ca-carbonate complexes
that inhibit U adsorption. The lowest concentrations are found in reducing groundwaters in equilibrium with uraninite and coffinite. Activities of Ra-226 and Pb-210, decay products of U-238, are only weakly correlated with U concentrations although
samplaes exceeding the standard for U generally exceed regulatory limits for Ra-226 (0.5 Bq/L) and Pb-210 (0.2 Bq/L) as well. In sub-oxic conditions Ra-226 is relatively more mobile than U whereas U and Pb-210 are more mobile in oxic groundwaters.
Natural mitigation of U at former mine sites is observed when discharge drains to organic-rich wetlands exhibiting reducing conditions. Where mine adits drain to nearby lakes, U may pose an environmental risk because of the mobility of
uranyl-Ca-carbonate complexes in oxic waters. |
Summary | (Plain Language Summary, not published) Small, low-grade, granite-hosted Uranium-Thorium-Rare Earth Element deposits are found throughout the Grenville geological province in Ontario, Québec
and Labrador. Renewed interest in this class of deposit, prompted by spikes in the price of uranium and the search for REE, has raised concerns about potential impacts to groundwater quality from mining activities. In order to inform public debate
and government decision making, NRCan scientists have investigated groundwater quality at historical mining sites in the Bancroft area, focusing on metals that may pose health risks. Results of this study show that elevated uranium concentrations are
derived from more soluble uranothorite, rather than uraninite, in the presence of carbonate species from calcite dissolution. Thorium, released concurrently with uranium, is immobilized close to its source. REE, from the dissolution of allanite and
other accessory minerals, occur at very low concentrations, mainly adsorbed on manganese precipitates. |
GEOSCAN ID | 305917 |
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