School of Earth Sciences - Theses
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ItemThe platinum-group element geochemistry and petrogenesis of the Heazlewood River mafic-ultramafic complex, Tasmania( 1990)The Heazlewood River mafic-ultramafic complex (HRC) comprises well-layered olivine- and orthopyroxene-rich cumulates, gabbronorite dykes, tonalites and low-Ti tholeiitic basalt and boninite lavas. The complex was emplaced as part of a large, low-angle thrust sheet during the middle Cambrian and subsequently deformed during the Devonian, so that the original stratigraphical relationships are obscured. The cumulate succession incorporates two distinct blocks, viz. the western HRC, comprising primitive adcumulates, and the eastern HRC, consisting of more evolved orthocumulates and mesocumulates. These two cumulate blocks are interpreted to represent stratigraphically equivalent parts of a single magma chamber. In this scenario, the western HRC represents an axial part of the intrusion where high heat flows, due to repeated injections of primitive magma, promoted the development of a compositionally zoned magma chamber. In contrast, the eastern HRC is believed to constitute a marginal facies of the intrusion, where sidewall cooling caused rapid crystallisation of successive magma additions and inhibited adcumulate growth and the formation of a compositionally stratified liquid column. Results from a detailed study of the mineral compositions and whole-rock geochemistry of the HRC suggest that all of the cumulates and most of the dykes and tonalites were derived from boninitic parental magmas. This hypothesis is substantiated by empirical models which were calculated using both major and trace element approaches. The models also show that the low-Ti basalts (second-stage melts) and boninites (third-stage melts) were probably derived from component-induced progressive partial melting of a MORB-depleted spinel lherzolite source. Partial melting of the refractory mantle source was initiated and sustained by the continued influx of slab-derived Si02-, LREE-, Zr-enriched hydrous fluids. The proposed petrogenetic model for the HRC is most consistent with an island arc setting for the complex, with melting occurring in MORB-depleted forearc lithosphere overlying a subduction zone. The HRC is not an ophiolite sensu stricto, despite the fact that it is more similar to the upper portions of the so-called 'island-arc ophiolites' (eg. Troodos) than to any other type of ultramafic intrusion. It is best perceived as a high-level boninitic magma chamber which developed immediately beneath a platform of genetically-related submarine lavas. The composition of the boninitic parental magmas was the principal control on the PGE geochemistry of the cumulate sequences. Despite representing PGE-enriched, S-undersaturated second-stage melts similar to the parental (U-type) magmas for the ultramafic portions of the Bushveld complex, the boninites were unable to form a Merensky-reef type PGE deposit because they did not come into contact with S-saturated (A-type) magmas. In the absence of cumulus sulphides, the PPGE (Pt, Pd, Rh) were partitioned into the residual liquids, whereas the IPGE (Os, Ir, Ru) were strongly fractionated into early-formed olivine-chromite cumulates. These features are highlighted by the extremely low IPGE tenor of the boninites, and the relatively high IPGE tenor of the dunites in comparison to the more evolved cumulates. Three types of chromitites are recognised in the HRC. Type I and type II chromitites occur as magmatic schlieren which probably formed during replenishment events. Type III chromitites occur as layers, pods and irregular patches developed in an unusual xenolith-bearing plagioclase peridotite. It is interpreted to have formed due to mixing between ascending xenolith-bearing, hydrous intercumulus liquids and resident ultramafic magma along the floor of the magma chamber. Chromitite occurrences in the HRC are enriched in PGE by up to two orders of magnitude relative to their ultramafic host rocks, and most strongly-enriched in Ru and/or Pt and Rh. Their PGE tenor reflects the early crystallisation of laurite, followed by Pt and Rh sulpharsenides, in response to increasing S and As activities which developed primarily due to magma mixing. The low Os and Ir abundances in the chromitites is believed to reflect their formation from Os- and Ir-depleted boninitic magmas. The HRC and the Adamsfield complex were the world's major suppliers of Os-Ir-Ru alloys during the early part of this century. The alloys occur in alluvial deposits that are spatially associated with primitive olivine-rich cumulate sequences. The latter are commonly suspected to represent the source for the alloys, but recent exploration programs have yet to define a bedrock occurrence of Os-Ir-Ru alloys in Tasmania. The results from the present study provide important constraints on the genesis of these alloys. Silicate inclusions found in the alloys suggest that they formed at mantle temperatures and pressures and were transported to crustal magma chambers by boninitic magmas. The alloys may have crystallised during ascent, or alternatively, represent residual mantle phases which became incorporated into the boninites during partial melting. Most of the observations pertaining to the Os and Ir geochemistry of the HRC suggest that the alloys probably occur in thin magmatic concentrations that were deposited along the base of the intrusion from the most primitive of the boninitic magmas involved in the generation of the cumulate sequences. Future exploration should focus on delineating the cumulate products of these primitive magmas and specifically, in defining the horizons which demarcate fresh influxes of these liquids.
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ItemMineralogy, geochemistry and origin of the Kalgoorlie gold deposits, Western Australia( 1978)Rich gold-telluride lodes (steeply dipping and flatly dipping) and minor gold-quartz stockwork mineralization characterize the Kalgoorlie gold-field. The origin of these gold deposits, the relationship between deposits and then nature of the host rocks are the major problems considered in this thesis. Extensive diamond drilling at the essentially unmineralized southern end of the field provided excellent material for stratigraphic studies and for country rock analysis whilst ore samples were obtained from both mines and drill core.
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ItemVolatile and precious metal geochemistry of the Mount Isa ores and their host rocks( 1986)Geochemical and petrographic investigations of Pb-Zn-Ag mineralization (12 orebody) and Cu-Co mineralization (1100 orebody) from Mount Isa were undertaken. Over one hundred and twenty carefully selected samples were analyzed for major and minor elements and for some or all of the following volatile metals: Au, Ag, Cd, As, Sb, Se, Bi, Co and Tl. A strong Tl enrichment is observed in (pyritic) unmineralized lateral equivalents of 12 orebody for several kilometers to the north of the mine sequence. The Se and As contents, S/Se ratios and S isotope relationships in the Pb-Zn ores and their host pyritic shales preclude a magmatic or deep-seated hydrothermal S Source. The data suggest that sulfide S in the Urquhart Shales was derived from reduction of a “seawater”/evaporitic/pore water sulfate source. Lateral variations in the thickness of mineralized intervals, the nature of the sulfide-gangue textures in the ores, the pervasive K and Tl enrichment in the host rocks and other chemical features of the Pb-Zn ores indicate that much of the Mount Isa mineralization formed epigenetically within the unconsolidated Urquhart Shales. The Pb-Zn-Ag ores contain very little Au and it is argued that this feature is best explained by the hydrothermal solutions that formed the Pb-Zn ores being cool (<<200°C) and moderately oxidized. The “silica dolomite” (the host to all the Mount Isa Cu mineralization) formed from “normal” Urquhart Shale as a result of intense fault-related hydrothermal activity (Perkins, 1984). The alteration has silicified the shales adjacent to the fault, and dolomite, phyllosilicates and “immobile” elements liberated during the silicification have been re-deposited at higher levels up-dip in the silica dolomite bodies. For the most part primary sulfide textures have not been preserved. It is argued that the distribution of several elements (notably Co, Bi, As, Fe and S) in 1100 orebody and its location down-dip from a strongly pyritic section of Urquhart shale are good evidence that stratiform Co (and Cu) mineralization was present in pyritic Urquhart Shales prior to formation of the silica dolomite. Chemical and isotopic evidence suggest that the Cu mineralization had a similar S-source and formed from similar solutions to the Pb-Zn-Ag ores. A new co-genetic model for the Mount Isa Cu and Pb-Zn-Ag deposits in which the mineralization formed from cool oxidized solutions in the upper few meters of the unconsolidated Urquhart Shales is presented. The metal-bearing solutions were expelled from their source rocks (oxidized clastic sediments lower in the Moust Isa Group) during the course of normal basin compaction and dewatering. Base metal sulfides were fixed by sulfate reduction processes occurring in the diagenetic environment of the Urquhart Shales. Weathered mafic volcanic detritus may have been and important component of the source.
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ItemThe geology, petrology and geochemistry of the Otway formation volcanogenic sediments( 1983)The geology, petrology and geochemistry of the Early Cretaceous Otway Formation have been investigated in detail and used to determ ine the nature of the source rocks and to develop a model for the diagenetic and low-grade metamorphic readjustments. The fluviatile Otway Formation was deposited in continental rift grabens that stretched some 1000 km along the southern coast of Australia during the Early Cretaceous. The main areas of deposition in the Otway, Gippsland and Bass Basins contain an estimated 100,000 cubic kilometres of detritus. The major part of this detritus was derived from pyroclastic material which has been shown by the fission track dating studies to have been derived from contemporaneous volcanism. The pile of volcanogenic material comprising the Otway Formation is at least 3 to 4 km thick in the main basins. The sediments are entirely non-marine and were deposited by large scale multichannel streams cut in extensive floodplains. The streams deposited thick multistorey channel sandstones in sheet-like bodies and a diverse spectrum of overbank mudstones and fine-grained sandstones. The complex channel sandstones fine upwards but have numerous erosional breaks indicating repeated flood cycles. Whereas the channel deposits have internal features consistent with braided stream channels the overall system has a large proportion of floodplain which was been considered in the past to have been a feature of meandering channels. The oversupply of volcanogenic detritus is considered to have been responsible for the development of the multiple channel depositional system in a climate of high seasonal rainfall. Whole rock chemical analyses of all lithologies in the sedimentary suite, recalculated i.nto a set of normative minerals, have proved useful in the distinction and description of sedimentary rocks in general. P20S was found to be useful for the identification of Early Cretaceous soil forming processes. The study of the chemical composition of detrital minerals has demonstrated the usefulness of this approach in the identification of the nature of the source magmas of volcanogenic sediments. For the Otway Formation, analyses of clinopyroxenes, amphiboles, feldspars and sphene in particular, have shown that high potassium dacitic to shoshonitic volcanism dominated during Early Cretaceous rifting. The new data on the geology and mineralogical and chemical features of the Otway Formation have application to the study of diagenesis and low-grade metamorphism in volcanogenic sediments in general. (From Abstract)