School of Earth Sciences - Theses
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ItemHydrogeology of the newer volcanic basalt aquifer at the Shell Terminal Newport Victoria( 2000-10)The Shell Terminal at Newport, Victoria and adjacent areas have been intensively used as terminals for large petroleum companies (BP,Ampol,Caltex, Mobil and Shell) for many years. As a consequence the groundwater is contaminated with light non-aquaeous phase liquids (LNAPLs) and an associated dissolved phase.
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ItemDetection of uranium(VI) in groundwater using a field electroanalytical technique( 1999)In this thesis electroanalytical methods are investigated and a new method developed to determine uranium(VI) in groundwater samples. Differential pulse polarography, differential pulse voltammetry and adsorptive stripping voltammetry methods, with appropriate mercury drop electrodes, were optimised using the adsorptive chelate 2,5-dichloro-3,6-dihydroxy-l,4-benzoquinone (chloranilic acid). An alternative adsorptive stripping voltammetry method, with a hanging mercury drop electrode, was optimised using the chelate 8-hydroxyquinoline (oxine). The liquid mercury requirements of these techniques limit their use in the field. Therefore, mercury film electrode methods that are potentially better suited to field conditions are investigated. Chloranilic acid was found to be a suitable chelating agent for uranium determination in combination with a hanging mercury drop electrode, but the reduction of chloranilic acid was a concern. A new mercury film electrode determination method using chloranilic acid was developed but was found to result in the deterioration of the MFE to the extent of rendering the method unsuitable for uranium determination. An adsorptive stripping voltammetry, MFE method with oxine was investigated. The inability to remove the uranyl-oxine reaction products from the MFE created a memory effect that contributed to a lack of accuracy and precision when performing standard addition determinations. This interference was a significant factor in the inability to reliably measure a uranium response using an adsorptive stripping potentiometry method with oxine. The technique of square wave adsorptive stripping voltammetry with oxine in combination with a hanging mercury drop electrode was found to be the most appropriate method for uranium determination. The method was fast, sensitive, precise and accurate when analysing standard solutions. A low detection limit of 2.7 µg/L was achieved. Groundwater and surface water samples were analysed by the AdSV, HMDE method with oxine. The mineral spring water samples from Daylesford, Victoria, were high in ionic content and contained interfering ions. The unacidified samples contained high concentrations of dissolved C02 that needed to be removed prior to sample analysis to prevent pH changes during analysis. Of six unacidified samples uranium was found in only one sample, the Tipperary Spring sample at 4.9 µg/L U(VI). Interference prevented confirmation of this concentration in the acidified Tipperary Spring sample. The construction of a linear standard addition plot with a positive x-intercept was a common outcome for both the unacidified and the acidified spring samples. The uranium concentration was determined in three surface water samples collected from the Ranger Uranium Mine in the Northern Territory. Matrix interference in these surface water samples resulted in non-linearity for two standard addition determinations. A third sample was successfully analysed to give a concentration of 23 µg/L U(VI), which is in good agreement with an independent determination. The unselective nature of oxine was found to result in significant interference when analysing environmental samples by the AdSV, HMDE method with oxine. This method was found to be inappropriate for field analysis of environmental samples. However, in a laboratory environment the AdSV, HMDE method with oxine was the best performing method when determining uranium in standard solutions.
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ItemThe geology and hydrogeology of the Corangamite region( 1971)Tectonic activity after the early Cretaceous resulted in a complete change in the depositional environment in the sedimentary basin - the Otway Basin - located to the south of the Western Highlands of Victoria and to the west of Melbourne. ThiS Basin became subject to increasing marine influences and the sediments deposited include thick sequences of Miocene marls: the Gellibrand Marl. The water in the marls and in the underlying sands of the Dilwyn Formation is saline near Lake Corangamite but elsewhere water of good quality is found in the sand aquifers, indicating that tectonic activity has caused the local isolation of the lower formation from the effects of flushing by fresher groundwater. Continued tectonic activity and associated volcanic activity during the Miocene and Lower Pliocene resulted firstly in the regression of the sea then the development of the internal drainage characteristic of the Corangamite Region. The sea probably retreated to the southeast as indicated by the unusual parallel physiographic features which have influenced the flows of 'earlier' Newer Volcanic lavas in the Curdie River area and the subsequent development of this river's drainage system. These features are probably related to remanent coast strandlines. The quality of the groundwater found in the 'earlier' lavas is generally poor but the basalts and tuffs of the 'later' Newer Volcanic age often contain water of low salinity, particularly in the intake areas which are located in the ‘stony rises' or near the volcanic cones. The intake area water of the Mt. Warrion basalts is a low salinity calcium-magnesium-bicarbonate water, having an unusually high nitrate content. As the salinity of the water increases away from the intake area the chemical nature of the water approaches that of a dilute sea water. This has been interpreted as being the result of a release of 'oceanic' connate salts by weathering of the calcareous material found in the tuffs and scoria beds of the volcanic cones. The material has been derived from the underlying marl sequence and has been incorporated into the igneous rocks during eruption. The high nitrate concentration has been attributed to the effects of pollution, since there is some evidence that the nitrate values have increased over the last sixty years, but there is also probably an increased rate of fixation in the intake area due to the effects of cultivation. The high bicarbonate values are probably due to a high rate of absorption of carbon dioxide from the atmosphere in the intake areas. The hydraulic characteristic of the basalts ensures the rapid distribution at the high nitrate and bicarbonate waters of the intake area over large areas, hence the effects of pollution are more readily noticeable. The groundwater regime plays an important role in the transfer of dissolved salts in the mainly saline water domain of the Corangamite Region. The study of the water and salt content of some of the lakes of the area indicates that a balance exists that results in the maintenance of a specific lake salinity within narrow limits, and in which the groundwater regime is often involved. By considering the salt balance and water balance of a system as one parameter, referred to as the Hydro Salinity Factor, a simple mathematical model can be postulated to determine some of the unknown factors involved in the maintenance of an equilibrium salinity in a lake. The drilling programme and groundwater investigation outlined an important water resource located in the Warrion area. Already 40 bores have been drilled in this area and they produce 6.6 x 105m3 /year (800 acre feet/year). There is an annual underflow of about 1.5 x 107 m3 (12,000 acre feet). This quantity is well within the 'safe yield' of the area and further development should be encouraged, but because of the presence of the large number of saline lakes in the area, saline water intrusion into the basalts would rapidly occur if the groundwater levels are lowered beneath the lake levels.
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ItemPhysical and chemical hydrogeology of the Otway Basin, southeast Australia( 2009)The Otway Basin of southeast Australia is the subject of this thesis, which incorporates pre-existing geological, hydraulic and major element hydrogeological data with new isotope hydrogeochemical investigations. The region is an Upper Cretaceous–Tertiary basin, filled with siliciclastic and calcareous aquifers and aquitards and characterised by late volcanic activity, pervasive faulting and karstification. (For complete abstract open document.) As part of this study, an hydrogeological database is compiled for the Otway Basin region from existing distinct datasets from the states of Victoria and South Australia. Utilising this new resource, the data are reinterpreted into a 3D model of the hydrostratigraphy for the basin in GoCAD, and interpolated surfaces of hydraulic head and electrical conductivity are created for 5 aquifers/aquitards. The Victorian hydraulic head data is analysed for long term declining or inclining trends and hydrograph trend maps are created for different aquifer systems. The data are also compiled into representative cross sections of flow and chemical composition, with one section located in each of the three major sub-basins. The records of groundwater chemistry from the Victorian section of the Otway Basin are used to plot the relative concentration of major cations and anions for the main aquifers. More than 120 groundwater samples were taken for analysis of major and minor ion concentration and/or oxygen, hydrogen, carbon, strontium and chlorine isotope composition. These data are used to characterise the hydrogeochemical evolution of the groundwater and to identify the processes that the groundwater drives or experiences in the system. The potentiometric maps and cross sections reveal the interconnected nature of the flow in all aquifers and the relationship between local and regional flow systems. Regional flow paths originate inland near basement highs or the basin margins. In the shallower aquifers they terminate at the coastline where the groundwater mixes with ocean water at a diffuse interface and density differences induce groundwater discharge at the land surface or the ocean floor. In the deeper confined aquifers, discharge is submarine via several possible mechanisms, which include: diffuse intergranular leakage to overlying units; flow along faults or volcanic conduits; and/or seepage directly to the ocean from exposed sections of the aquifer, e.g. in submarine canyons. These mechanisms may be operating up to 50 km offshore but the interface is currently migrating landward, which will result in a shortening of that estimated distance. Local-scale flow lines are complex and may be oriented against the direction of regional coastward flow. Local hydraulic divides are often associated with volcanic eruption centres, which have elevated topography and relatively high hydraulic head, making them important recharge zones. These zones contain low salinity groundwater because infiltration is relatively rapid. Conversely, basalt flows that have developed clay horizons through weathering reduce drainage and allow significant evapotranspiration which concentrates the cyclic salts in solution. Many local flow systems discharge mainly via evapotranspiration, which acts again to concentrate the cyclic salts in solution. Other local discharge zones are rivers, creeks and lakes or lagoons that receive baseflow and seeps and springs associated with geological contacts or boundaries and faults. Evaporitic concentration of solutes in surface water bodies and shallow groundwater affects the quality of water recharging the underlying aquifers and aquitards. This quality has changed over the last 50,000 years or so due to fluctuations in climate and hence variation of the precipitation/evaporation ratio. Stresses on the aquifers are climate fluctuations, sea level change, land use change and groundwater extraction. These stresses have resulted in the system being out of hydraulic equilibrium in many cases. Lags in response to these changes in boundary conditions are identified and/or hypothesised. In particular, the confined aquifer’s response to sea level change could be subject to a lag in the order of millennia. The stress on an aquifer is often transferred to its adjacent units, in some cases inducing cross-formational leakage, which is possibly supported by radiocarbon dating evidence. The area of the Otway Ranges appears to have escaped the effects of stress to date because of its stable microclimate, its distance from the ocean and from groundwater extraction. Increase in demand on groundwater resources, development of geothermal, sequestration and hydrocarbon industries and future climate change may yet have a detrimental effect on the groundwater of the Otway Basin. Isotopic composition of the groundwater confirms its meteoric origin and chlorine isotopes from several samples of the deep groundwater indicate that accumulation of solutes along the flow path is not due to diffusion or dissolution of connate salt. Thus, the salinity of the water is sourced from cyclic salts and solutes from water-rock interaction, both of which may be concentrated by evapotranspiration. Water-rock interaction is dominated by dissolution of carbonates and weathering of silicates as a result of the surficial geology being dominated by calcarenite or limestone and young basalt. The volcanic activity has produced gas that has interacted with the groundwater, and continues to do so, fractionating oxygen, hydrogen and carbon isotopes and contributing fluorine, boron and sulphur to solution. The addition of volcanic CO2 creates an uncommon situation for water-rock interaction, where continued dissolution of carbonate and silicate minerals along the deeper flow paths is demonstrated by the silicon/chloride ratios and strontium isotopic composition of the groundwater. These water-rock interaction processes, with the addition of cation exchange, are responsible for the development of a relatively fresh Na+HCO− 3 type water that is characteristic in parts of the deep aquifer. The study confirms the existing hydrogeological understanding of the Otway Basin and forms new conclusions regarding the history of the groundwater and the processes of flow and chemical evolution by integrating numerous lines of evidence. Significant contributions of this work which improve current scientific knowledge include these findings: the maps and cross sections of hydraulic head and electrical conductivity reveal the connected nature of flow systems within all the aquifers and aquitards; geological features can induce discharge, e.g. at contacts or faults, and recharge, e.g. volcanic eruption centres; the changes to the surface drainage system as a result of the eruption of basalt flows have affected the water chemistry and flow systems in all the underlying units; there is a lag in aquifers’ responses to sea level change and therefore future migration of the interface is expected regardless of further boundary changes; climate change has influenced surface water quality by changing the regional water balance, and therefore has affected groundwater quality; the discharge from the confined aquifer is submarine via various pathways, interaction between the groundwater and volcanic gas has occurred in the past and is ongoing, and consequently mineral dissolution persists at deep levels; the origin of high salinity of brackish groundwater in all Tertiary aquifers and aquitards is concentrated solutes from water rock interaction and cyclic deposition.