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Conference Proceedings

Water in Mining 2009

Conference Proceedings

Water in Mining 2009

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The Use of Stable Isotopes of Oxygen, Hydrogen and Carbon to Understand Groundwater Dynamics in the Hamersley Basin, Western Pilbara Region, Northwest Australia

Major ions, d18O and d2H and Carbon-13 concentrations in groundwater from 30 bores near an open pit iron ore mine were used to better understand the chemical evolution of groundwater in the aquifer. The relatively depleted d18O and d2H isotopes of groundwater from various depths suggest that groundwater is recharged from intense rainfall events, with little evaporative effect. The 300 to 500 mg/L increase of major ions relative to that of rainfall is due to evapotranspiration of rainfall during recharge. Geochemical mass balance modelling suggests that the evapotranspiration of rainfall during infiltration through the unsaturated zone varies over six fold from 20 to 130._x000D_
This coupled with the dissolution of CO2 from the unsaturated zone and partial dissolution of carbonates and gypsum from Tertiary sediments and carbonates from the Wittenoom Formation accounts for the current major ion, d18O and d2H distribution in groundwater. Despite the relatively dissected morphology and steep hydraulic gradient the results of this study highlight the dominance of vertical flow relative to horizontal flow. The study also shows the dominance of rapid recharge by significant rainfall events as an important component of the water budget for east Pilbara aquifers._x000D_
FORMAL CITATION:Dogramaci, S and Dodson, W, 2009. The use of stable isotopes of oxygen, hydrogen and carbon to understand groundwater dynamics in the Hamersley Basin, Western Pilbara Region, northwest Australia, in Proceedings Water in Mining 2009, pp 89-98 (The Australasian Institute of Mining and Metallurgy: Melbourne).
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  • The Use of Stable Isotopes of Oxygen, Hydrogen and Carbon to Understand Groundwater Dynamics in the Hamersley Basin, Western Pilbara Region, Northwest Australia
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  • Published: 2009
  • PDF Size: 0.532 Mb.
  • Unique ID: P200910011

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