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Groundwater geochemistry,hydrogeology and potash mineral potential of the Lake Woods region,Northern Territory,Australia
Authors:P de Caritat  E N Bastrakov  S Jaireth  P M English  J D A Clarke  T P Mernagh
Institution:1. Geoscience Australia, GPO Box 378, Canberra, ACT 2601, Australia;2. Research School of Earth Sciences, The Australian National University, Canberra, ACT 2601, Australia;3. Formerly at: Geoscience Australia, Canberra, Australia;4. Present address: Aranda, ACT 2614, Australia;5. Present address: Monash, ACT 2904, Australia;6. Research School of Earth Sciences, The Australian National University, Canberra, ACT 2601, Australia;7. Formerly at: Geoscience Australia, Canberra, Australia
Abstract:We 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.
Keywords:Groundwater  hydrogeochemistry  mineral systems  potash  processes  Australia
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