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dc.contributor.authorFoulkes, M
dc.contributor.authorMillward, G
dc.contributor.authorHenderson, S
dc.contributor.authorBlake, William
dc.date.accessioned2017-03-02T10:43:27Z
dc.date.available2017-03-02T10:43:27Z
dc.date.issued2016-12-12
dc.identifier.issn0265-931X
dc.identifier.issn1879-1700
dc.identifier.urihttp://hdl.handle.net/10026.1/8579
dc.description.abstract

Bioaccessible U, Th, Pb and the 238U decay products 214Pb and 210Pb have been determined, using a modified Unified BARGE Method (UBM), in waste solids and soils from an abandoned uranium mine in South West England, UK. Maximum aqua regia extractable concentrations for U, Th and Pb were 16,200, 3.8 and 4750 μg g-1, respectively. 238U had highest activity concentrations near the mine shaft, where the decay products214Pb and 210Pb had values of 235 and 180 Bq g-1, respectively. UBM extractions gave mean gastro-intestinal bioaccessibility factors (BAFs) for U and Pb in the waste solids of 0.05 and 0.03, respectively, whereas those for the soils were significantly higher at 0.24 and 0.17. The mean BAFs for the transient radionuclides, 214Pb and 210Pb, were similar to those for stable Pb implying that the stable and radioactive Pb isotopes were attached to similar sites on the particles. The doses arising from the ingestion of particulate 210Pb due to soil pica behaviour were in the range 0.2-65 and < 0.1-6.2 μSv day-1 for a 1-year old child or an adult (>17 years), respectively. The results suggest that the health risk posed by abandoned uranium mines, with waste rock and tailings, throughout the world should take account of the dose due to both bioaccessible radionuclides, as well as their stable counterparts.

dc.format.extent85-96
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherElsevier BV
dc.subjectUranium
dc.subjectMine
dc.subjectSolid wastes
dc.subjectRadioactivity
dc.subjectBioaccessibility
dc.subjectDose
dc.titleBioaccessibility of U, Th and Pb in solid wastes and soils from an abandoned uranium mine
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000401675800013&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.volume173
plymouth.publication-statusPublished
plymouth.journalJournal of Environmental Radioactivity
dc.identifier.doi10.1016/j.jenvrad.2016.11.030
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Admin Group - REF
plymouth.organisational-group/Plymouth/Admin Group - REF/REF Admin Group - FoSE
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering/School of Geography, Earth and Environmental Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA14 Geography and Environmental Studies
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plymouth.organisational-group/Plymouth/Research Groups/Marine Institute
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dc.publisher.placeEngland
dcterms.dateAccepted2016-11-27
dc.rights.embargodate2017-12-12
dc.identifier.eissn1879-1700
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1016/j.jenvrad.2016.11.030
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2016-12-12
rioxxterms.typeJournal Article/Review


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