Genesis and evolution of the lithospheric mantle beneath the Buffalo Head Terrane, Alberta (Canada)

Mantle xenoliths and xenocrysts were retrieved from three of the 88–86 Ma Buffalo Hills kimberlites (K6, K11, K14) for a reconnaissance study of the subcontinental lithospheric mantle (SCLM) beneath the Buffalo Head Terrane (Alberta, Canada). The xenoliths include spinel lherzolites, one garnet spinel lherzolite, garnet harzburgites, one sheared garnet lherzolite and pyroxenites. Pyroxenitic and wehrlitic garnet xenocrysts are derived primarily from the shallow mantle and lherzolitic garnet xenocrysts from the deep mantle. Harzburgite with Ca-saturated garnets is concentrated in a layer between 135–165 km depth. Garnet xenocrysts define a model conductive paleogeotherm corresponding to a heat flow of 38–39 mW/m². The sheared garnet lherzolite lies on an inflection of this geotherm and may constrain the depth of the lithosphere–asthenosphere boundary (LAB) beneath this region to ca 180 km depth.

A loss of >20% partial melt is recorded by spinel lherzolites and up to 60% by the garnet harzburgites, which may be related to lithosphere formation. The mantle was subsequently modified during at least two metasomatic events. An older metasomatic event is evident in incompatible-element enrichments in homogeneous equilibrated garnet and clinopyroxene. Silicate melt metasomatism predominated in the deep lithosphere and led to enrichments in the HFSE with minor enrichments in LREE. Metasomatism by small-volume volatile-rich melts, such as carbonatite, appears to have been more important in the shallow lithosphere and led to enrichments in LREE with minor enrichments in HFSE. An intermediate metasomatic style, possibly a signature of volatile-rich silicate melts, is also recognised. These metasomatic styles may be related through modification of a single melt during progressive interaction with the mantle. This metasomatism is suggested to have occurred during Paleoproterozoic rifting of the Buffalo Head Terrane from the neighbouring Rae Province and may be responsible for the evolution of some samples toward unradiogenic Nd and Hf isotopic compositions.

Disturbed Re–Os isotope systematics, evident in implausible model ages, were obtained in situ for sulfides in several spinel lherzolites and suggest that many sulfides are secondary (metasomatic) or mixtures of primary and secondary sulfides. Sulfide in one peridotite has unradiogenic ¹⁸⁷Os/¹⁸⁸Os and gives a model age of 1.89±0.38 Ga. This age coincides with the inferred emplacement of mafic sheets in the crust and suggests that the melts parental to the intrusions interacted with the lithospheric mantle.

A younger metasomatic event is indicated by the occurrence of sulfide-rich melt patches, unequilibrated mineral compositions and overgrowths on spinel that are Ti-, Cr- and Fe-rich but Zn-poor. Subsequent cooling is recorded by fine exsolution lamellae in the pyroxenes and by arrested mineral reactions.

If the lithosphere beneath the Buffalo Head Terrane was formed in the Archaean, any unambiguous signatures of this ancient origin may have been obliterated during these multiple events.     

Spatial Concentration in Australian Regional Development,Exogenous Shocks and Regional Demographic Outcomes: a South Australian case study

ABSTRACT

As a tribute to the massive contribution of our friend and colleague Graeme Hugo to the population and settlement geography of Australian rural areas, this paper presents a longitudinal study from his home State. It forms part of a wider study of the long-term demographic relationships between Australia’s rapidly growing regional cities and their surrounding functional regions. Of particular interest is the question of what effect the accelerating concentration of population and economic activity into a given regional city will have for the longer term demographic sustainability of its functional region as a whole. Taking the case of Port Lincoln, regional capital of most of South Australia’s Eyre Peninsula, it examines the nature of change in the functional region over the period 1947–2011, and investigates the forces feeding, and partly counteracting, the population concentration process, informed by concepts of evolutionary economic geography. In particular it traces the demographic impact (particularly differential migration and ageing trends) of exogenous shocks to the region’s essentially primary productive economic base during the period of major change from 1981 to 2011.     

Characterisation of primary and secondary carbonates in hypabyssal kimberlites: an integrated compositional and Sr-isotopic approach

Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable ⁸⁷Sr/⁸⁶Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted ⁸⁷Sr/⁸⁶Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with ⁸⁷Sr/⁸⁶Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.

     

Daily variability of dissolved inorganic radiocarbon at three sites in the surface ocean

We report radiocarbon measurements of dissolved inorganic carbon (DIC) in surface water samples collected daily during cruises to the central North Pacific, the Sargasso Sea and the Southern Ocean. The ranges of Δ¹⁴C measurements for each cruise (11–30‰) were larger than the total uncertainty (7.8‰, 2-sigma) of the measurements. The variability is attributed to changes in the upper water mass that took place at each site over a two to four week period. These results indicate that variability of surface Δ¹⁴C values is larger than the analytical precision, because of patchiness that exists in the DIC Δ¹⁴C signature of the surface ocean. This additional variability can affect estimates of geochemical parameters such as the air–sea CO₂ exchange rate using radiocarbon.     

Trace‐element signatures of apatites in granitoids from the Mt Isa Inlier,northwestern Queensland

The concentrations of trace elements in apatite from granitoid rocks of the Mt Isa Inlier have been investigated using the laser‐ablation inductively coupled plasma‐mass spectrometry (ICP‐MS) microprobe. The results indicate that the distribution of trace elements (especially rare‐earth elements (REE), Sr, Y, Mn and Th) in apatite strongly reflects the chemical characteristics of the parental rock. The variations in the trace‐element concentrations of apatite are correlated with parameters such as the SiO₂ content, oxidation state of iron, total alkalis and the aluminium saturation index (ASI). The relative enrichment of Y, HREE and Mn and the relative depletion of Sr in the apatites studied reflect the degree of fractionation of the host granite. Apatites from strongly oxidised plutons tend to have higher concentrations of LREE relative to MREE. Manganese concentrations are higher in apatite from reduced granitoids because Mn²⁺substitutes directly for Ca²⁺. The La/Ce ratio of apatite is well‐correlated with the whole‐rock K²O and Na²O contents, as well as with the oxidation state and ASI. Because apatite trace‐element composition reflects the chemistry of the whole rock, it can be a useful indicator mineral for the recognition of mineralised granite suites, where particular mineralisation styles are associated with granitoids that have specific geochemical fingerprints.     

Chronology of the pressure-temperature history recorded by a granulite terrain

Coronite-bearing anorthositic granulites consisting of olivine, orthopyroxene, clinopyroxene, garnet and plagioclase assemblages are particularly well preserved at Gaupås and Holsnöy in the Bergen Arc of West Norway. The coronites are considered to have formed near T= 900° C and P=10 Kb by two stages of subsolidus reaction from an anorthositic gabbro parent. The first reaction involved ol+plagcpxI+opxI+sp and the second cpxI+opxI+sp+plcpxII+opxII+gn. The incomplete reaction products are preserved to varying extents in different corona structures. Sm-Nd isotopic data for each of four coronas yield precise isochrons, and demonstrate isochronism both between the constituent phases of the corona assemblages and dispersed ground mass phases. Three individual coronas not associated with shear zones yield ages of 907±9 my, 912±18 my and 905±37 my. Eclogite facies mineralogy is developed locally in shear zones, which are shown by Sm-Nd and Rb-Sr analyses to be Caledonian in age. Where relict corona structures survive unsheared within these zones, Nd exchange between the constituent phases cannot be resolved. This observation together with sympathetic Ca/Mg and Sm/Nd zoning preserved at T900° C in the garnet mantles of coronites places a limit on the diffusivity of Nd in pyropic garnets which is no higher than published experimental values for Mg in pyrope-almandine garnets. Consequently even in slowly-cooled granulite terrains, garnet grains are expected to yield Sm-Nd chronologies very close to the time of mineral growth.     

Limitations and feasibility of the land disposal of organic solvent-contaminated wastes

The limitations and feasibility of the land disposal of solid wastes containing organic solvents and refrigerants (chlorinated fluorocarbons) were investigated by evaluating the attenuation capacity of a hypothetical waste-disposal site by numerical modeling. The basic theorem of this approach was that the land disposal of wastes would be environmentally acceptable if subsurface attenuation reduced groundwater concentrations of organic compounds to concentrations that were less than health-based, water-quality criteria. Computer simulations indicated that the predicted concentrations of 13 of 33 organic compounds in groundwater would be less than their health-based criteria. Hence, solid wastes containing these compounds could be safely disposed at the site. The attenuation capacity of the site was insufficient to reduce concentrations of four compounds to safe levels without limiting the amount of mass available to leach into groundwater. Threshold masses based on time-dependent migration simulations were estimated for these compounds. The remaining 16 compounds, which consisted mainly of chlorinated hydrocarbons and fluorocarbons could not be safely landfilled without severe restrictions on the amounts disposed. These organic compounds were candidates to ban from land disposal.     

Crystal features of supergene gold at Hannan South,Western Australia

Deep weathering of basalt-hosted sulphidic gold mineralisation has resulted in remobilisation of the gold and the formation of a supergene deposit. The deposit occurs beneath an ephemeral lake system and is at least partially saturated by highly saline groundwater. A general downward movement of an iron redox front associated with the weathering has controlled the distribution of the gold and its morphology. It is unusual in that the high fineness gold crystals formed are coarse and well-preserved. Small octahedra, up to 50 μm, are the most abundant form of gold crystals but large, up to 3 mm, octahedral plates are common. Crystal morphology variations described here suggest that the gold is initially precipitated as euhedral octahedra and plates. Subsequent dissolution and recrystallisation associated with fluctuations in the chemical environment above the redox front has led to the development of the more common irregular dendritic or wire gold forms observed in other supergene deposits.     

Geology-based conditional simulation in the Athabasca oil sands deposit,Alberta, Canada

The Athabasca oil sands deposit, Alberta, Canada, is one of the largest known hydrocarbon accumulations. The efficient exploitation of this deposit, as well as other oil sand accumulations throughout the world, is based onin situ recovery and surface mining methods. Quantitative modeling of deposit heterogeneity provides a valuable engineering tool. In the present study, conditional simulation was used to model oil-saturated zones in part of the Athabasca deposit. This technique generates equiprobable models of thein situ variability of essential deposit attributes that honor the available data and their spatial statistics. The application of the technique is based on the delineation of geologically homogeneous zones within the host McMurray Formation, their statistical validity, and the integration of geological interpretations. The geological framework is developed, and subsequently, high resolution conditionally simulated models of three identified hydrocarbon-bearing zones are generated, in terms of the zone boundaries and the percent weight of oil saturation. These models serve as “what-if” tools for risk assessment and future planning.     

Residence of trace elements in metasomatized spinel lherzolite xenoliths: a proton-microprobe study

Minerals occurring in dry and modally metasomatized spinel lherzolites from western Victoria have been analysed by proton microprobe for Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Ba, Pb, Br, rare-earth elements (REE), Th and U. Mass-balance calculations demonstrate that these trace elements are contained in specific acceptor minerals and do not occur in significant concentrations at clean grain boundaries. The level of particular trace elements in the rock depends on the presence of specific phases: for example high levels of REE, Sr (and U, Th, Br) require apatite, while Ba, Nb and Ta are strongly concentrated in amphibole±mica. Mantle metasomatism in these spinel lherzolites is inferred to result from an open-system process involving infiltration of fluids released by crystallizing silicate melts. This process produces metasomatic zones with different modal mineralogy and hence greatly different trace-element signatures. The data demonstrate that large-ion-lithophile (LIL) and high-field strength (HFS) elements in metasomatized spinel lherzolites are strongly concentrated in non-refractory phases, which will break down easily in heated volumes such as the walls of magma conduits. The heterogeneity observed in trace-element patterns of intraplate alkali basaltic rocks may not reflect source heterogeneity, but may result largely from contamination by metasomatized mantle wall rock. The K_Ds for most trace elements show little temperature dependence except for K_DSr between orthopyroxene and clinopyroxene where K_D decreases with increasing temperature. The generally uniform K_Ds can be used to test for disequilibrium in such assemblages.