Publicação:
Dissolved uranium, radium and radon evolution in the Continental Intercalaire aquifer, Algeria and Tunisia

dc.contributor.authorElliot, Trevor
dc.contributor.authorBonotto, Daniel Marcos [UNESP]
dc.contributor.authorAndrews, John Napier
dc.contributor.institutionQueens Univ Belfast
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Bath
dc.date.accessioned2015-03-18T15:53:34Z
dc.date.available2015-03-18T15:53:34Z
dc.date.issued2014-11-01
dc.description.abstractNatural, dissolved U-238-series radionuclides (U, Ra-226, Rn-222) and activity ratios (A.R.s: U-234/U-238; Ra-228/Ra-226) in Continental Intercalaire (Cl) groundwaters and limited samples from the overlying Complexe Terminal (CT) aquifers of Algeria and Tunisia are discussed alongside core measurements for U/Th (and K) in the contexts of radiological water quality, geochemical controls in the aquifer, and water residence times. A redox barrier is characterised downgradient in the Algerian Cl for which a trend of increasing U-234/U-238 A.R.s with decreasing U-contents due to recoil-dominated U-234 solution under reducing conditions allows residence time modelling similar to 500 ka for the highest enhanced A.R. = 3.17. Geochemical modelling therefore identifies waters towards the centre of the Grand Erg Oriental basin as palaeowaters in line with reported C-14 and Cl-36 ages. A similar U-234/U-238 trend is evidenced in a few of the Tunisian CI waters. The paleoage status of these waters is affirmed by both noble gas recharge temperatures and simple modelling of dissolved, radiogenic He-4-contents both for sampled Algerian and Tunisian CI and CT waters. For the regions studied these waters therefore should be regarded as "fossil" waters and treated effectively as a non-renewable resource. (C) 2014 The Authors. Published by Elsevier Ltd.en
dc.description.affiliationQueens Univ Belfast, Sch Planning Architecture & Civil Engn, Environm Tracers Lab, Belfast BT9 5AG, Antrim, North Ireland
dc.description.affiliationIGCE UNESP, Dept Petrol & Metalogenia, BR-13506900 Rio Claro, SP, Brazil
dc.description.affiliationUniv Bath, Sch Chem, Bath BA2 7AY, Avon, England
dc.description.affiliationUnespIGCE UNESP, Dept Petrol & Metalogenia, BR-13506900 Rio Claro, SP, Brazil
dc.description.sponsorshipUK Natural Environment Research Council NERC
dc.description.sponsorshipIdUK Natural Environment Research Council NERCGT/84/AAPS/58
dc.format.extent150-162
dc.identifierhttp://dx.doi.org/10.1016/j.jenvrad.2014.07.003
dc.identifier.citationJournal Of Environmental Radioactivity. Oxford: Elsevier Sci Ltd, v. 137, p. 150-162, 2014.
dc.identifier.doi10.1016/j.jenvrad.2014.07.003
dc.identifier.fileWOS000343628100021.pdf
dc.identifier.issn0265-931X
dc.identifier.lattes7430102726026121
dc.identifier.urihttp://hdl.handle.net/11449/116598
dc.identifier.wosWOS:000343628100021
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal Of Environmental Radioactivity
dc.relation.ispartofjcr2.263
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectUranium isotopesen
dc.subjectRadiogenic heliumen
dc.subjectNoble gas recharge temperaturesen
dc.subjectGroundwater agesen
dc.subjectContinental Intercalaire & Complexeen
dc.subjectTerminal aquifersen
dc.subjectAlgeria & Tunisiaen
dc.titleDissolved uranium, radium and radon evolution in the Continental Intercalaire aquifer, Algeria and Tunisiaen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes7430102726026121
unesp.author.orcid0000-0001-6452-9809[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Geociências e Ciências Exatas, Rio Claropt
unesp.departmentPetrologia e Metalogenia - IGCEpt

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