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Groundwater geochemistry, hydrogeology and potash mineral potential of the Lake Woods region, Northern Territory, Australia

dc.contributor.authorde Caritat, Patrice
dc.contributor.authorBastrakov, Evgeniy N.
dc.contributor.authorJaireth, S.
dc.contributor.authorEnglish, P.M.
dc.contributor.authorClarke, J D A
dc.contributor.authorMernagh, Terrence
dc.contributor.authorWygralak, A S
dc.contributor.authorDulfer, H. E.
dc.contributor.authorTrafford, J.M.
dc.date.accessioned2020-04-01T00:42:42Z
dc.date.available2020-04-01T00:42:42Z
dc.date.issued2019
dc.date.updated2019-11-25T07:46:39Z
dc.description.abstractWe collected 38 groundwater and two surface-water samples in the semi-arid Lake Woods region of the Northern Territory to better understand the hydrogeochemistry of this system, which straddles the Wiso, Tennant Creek and Georgina geological regions. Lake Woods is presently a losing waterbody feeding the underlying groundwater system. The main aquifers comprise mainly carbonate (limestone and dolostone), siliciclastic (sandstone and siltstone) and evaporitic units. The water composition was determined in terms of bulk properties (pH, electrical conductivity, temperature, dissolved oxygen, redox potential), 40 major, minor and trace elements, and six isotopes (δ18Owater, δ2Hwater, δ13CDIC, δ34SSO42–, δ18OSO42–, 87Sr/86Sr). The groundwater is recharged through infiltration in the catchment from monsoonal rainfall (annual average rainfall ∼600 mm) and runoff. It evolves geochemically mainly through evapotranspiration and water–mineral interaction (dissolution of carbonates, silicates and to a lesser extent sulfates). The two surface waters (one from the main creek feeding the lake, the other from the lake itself) are extraordinarily enriched in 18O and 2H isotopes (δ18O of +10.9 and +16.4‰ VSMOW, and δ2H of +41 and +93‰ VSMOW, respectively), which is interpreted to reflect evaporation during the dry season (annual average evaporation ∼3000 mm) under low humidity conditions (annual average relative humidity ∼40%). This interpretation is supported by modelling results. The potassium (K) relative enrichment (K/Cl– mass ratio over 50 times that of sea water) is similar to that observed in salt-lake systems worldwide that are prospective for potash resources. Potassium enrichment is believed to derive partly from dust during atmospheric transport/deposition, but mostly from weathering of K-silicates in the aquifer materials (and possibly underlying formations). Further studies of Australian salt-lake systems are required to reach evidence-based conclusions on their mineral potential for potash, lithium, boron and other low-temperature mineral system commodities such as uranium.en_AU
dc.description.sponsorshipThis project was undertaken as part of the salt-lake mineral prospectivity project at Geoscience Australia during 2012–2013, which was supported by appropriation funding from the Commonwealth of Australiaen_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0812-0099en_AU
dc.identifier.urihttp://hdl.handle.net/1885/202575
dc.language.isoen_AUen_AU
dc.provenance© 2019 Crown Copyright in the Commonwealth of Australia Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_AU
dc.publisherTaylor & Francisen_AU
dc.rights© 2019 Crown Copyright in the Commonwealth of Australia Published by Informa UK Limited, trading as Taylor & Francis Groupen_AU
dc.rights.licenseCreative Commons Attribution Licenseen_AU
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_AU
dc.sourceAustralian Journal of Earth Sciencesen_AU
dc.titleGroundwater geochemistry, hydrogeology and potash mineral potential of the Lake Woods region, Northern Territory, Australiaen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue3en_AU
local.bibliographicCitation.lastpage430en_AU
local.bibliographicCitation.startpage411en_AU
local.contributor.affiliationDe Caritat, Patrice, College of Science, ANUen_AU
local.contributor.affiliationBastrakov, Evgeniy N., Geoscience Australiaen_AU
local.contributor.affiliationJaireth, S., Geoscience Australiaen_AU
local.contributor.affiliationEnglish, P.M., Geoscience Australiaen_AU
local.contributor.affiliationClarke, J D A, Monash Universityen_AU
local.contributor.affiliationMernagh, Terrence, College of Science, ANUen_AU
local.contributor.affiliationWygralak, A S, Northern Territory Geological Surveyen_AU
local.contributor.affiliationDulfer, H. E., Charles Universityen_AU
local.contributor.affiliationTrafford, J.M., Geoscience Australiaen_AU
local.contributor.authoruidDe Caritat, Patrice, u3702178en_AU
local.contributor.authoruidMernagh, Terrence, u5645128en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor040201 - Exploration Geochemistryen_AU
local.identifier.absseo961404 - Mining Soilsen_AU
local.identifier.absseo840199 - Mineral Exploration not elsewhere classifieden_AU
local.identifier.ariespublicationu3102795xPUB951en_AU
local.identifier.citationvolume66en_AU
local.identifier.doi10.1080/08120099.2018.1543208en_AU
local.identifier.scopusID2-s2.0-85060548311
local.publisher.urlhttps://www.routledge.com/en_AU
local.type.statusPublished Versionen_AU

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