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Nitrate-dependent Uranium mobilisation in groundwater

dc.contributor.authorBonotto, Daniel Marcos [UNESP]
dc.contributor.authorWijesiri, Buddhi
dc.contributor.authorGoonetilleke, Ashantha
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionShenzhen University
dc.contributor.institutionQueensland University of Technology (QUT)
dc.date.accessioned2020-12-12T01:42:10Z
dc.date.available2020-12-12T01:42:10Z
dc.date.issued2019-11-25
dc.description.abstractNitrate is a critical substance that determines the prevailing redox conditions in groundwater, and in turn the behaviour of Uranium (U). Therefore, the excessive use of nitrate-fertiliser in agricultural catchments could exert a significant influence on U mobilisation. This is a significant issue in catchments, where groundwater resources are increasingly being exploited for drinking water production. Past studies on U mobility in groundwater have considered individual hydro-geochemical factors influencing U concentrations, rather than as a single system with multiple factors. This research study investigated nitrate-dependent U mobility within a catchment in Brazil, where a range of intensive agricultural activities are undertaken and the giant Guarani aquifer is located. The study used direct measurements of groundwater redox conditions and other hydro-geochemical parameters. The research outcomes indicated that U could have two hydro-geochemical systems based on positive and negative redox potential of groundwater. The pH, HCO3 − and temperature pose the largest influence, respectively, on U mobilisation, and these impacts are greater in agricultural lands than urban areas. Acidic and less reducing (positive redox) groundwater across the aquifer and basic and highly reducing (negative redox) groundwater in agricultural areas make U more mobile. The alkalinity increases U mobility in less reducing groundwater across the aquifer and in highly reducing groundwater in agricultural areas. Further, U can be mobile in hot and less reducing groundwater across the aquifer, but hot and highly reducing groundwater in agricultural areas can limit U mobility. More importantly, the study revealed that U can be mobile under high NO3 − concentrations in reducing groundwater in non-agricultural areas. However, anthropogenic inputs of NO3 − are expected to be lower than natural NO3 − inputs in areas where the groundwater is highly reducing. Hence, fertiliser use in agricultural lands is less likely to increase U mobility in highly reducing groundwater.en
dc.description.affiliationDepartamento de Petrologia e Metalogenia Universidade Estadual Paulista (UNESP), Câmpus de Rio Claro, Av. 24-ANo.1515, C.P. 178
dc.description.affiliationCollege of Chemistry and Environmental Engineering Shenzhen University
dc.description.affiliationScience and Engineering Faculty Queensland University of Technology (QUT), GPO Box 2434
dc.description.affiliationUnespDepartamento de Petrologia e Metalogenia Universidade Estadual Paulista (UNESP), Câmpus de Rio Claro, Av. 24-ANo.1515, C.P. 178
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2016/50327-4
dc.identifierhttp://dx.doi.org/10.1016/j.scitotenv.2019.133655
dc.identifier.citationScience of the Total Environment, v. 693.
dc.identifier.doi10.1016/j.scitotenv.2019.133655
dc.identifier.issn1879-1026
dc.identifier.issn0048-9697
dc.identifier.scopus2-s2.0-85073649863
dc.identifier.urihttp://hdl.handle.net/11449/199520
dc.language.isoeng
dc.relation.ispartofScience of the Total Environment
dc.sourceScopus
dc.subjectDrinking water
dc.subjectGeochemistry
dc.subjectGroundwater
dc.subjectNitrates
dc.subjectRedox potential
dc.subjectUranium
dc.titleNitrate-dependent Uranium mobilisation in groundwateren
dc.typeArtigo
unesp.author.orcid0000-0003-1504-1836 0000-0003-1504-1836[2]
unesp.author.orcid0000-0002-8783-1223[3]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Geociências e Ciências Exatas, Rio Claropt
unesp.departmentPetrologia e Metalogenia - IGCEpt

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