This web service delivers datasets produced by the Critical Minerals Mapping Initiative (CMMI), a collaboration between Geoscience Australia (GA), the Geological Survey of Canada (GSC) and the United States Geological Survey (USGS). Data in this service includes geochemical analyses of over 7000 samples collected from or near mineral deposits from 60 countries, and mineral prospectivity models for clastic-dominated (Zn, Pb) and Mississippi Valley-type (Zn-Pb) deposits across Canada, the United States, and Australia.

This web service delivers datasets produced by the Critical Minerals Mapping Initiative (CMMI), a collaboration between Geoscience Australia (GA), the Geological Survey of Canada (GSC) and the United States Geological Survey (USGS). Data in this service includes geochemical analyses of over 7000 samples collected from or near mineral deposits from 60 countries, and mineral prospectivity models for clastic-dominated (Zn, Pb) and Mississippi Valley-type (Zn-Pb) deposits across Canada, the United States, and Australia.

Although critical minerals (CMs) are currently produced from existing mines, their distributions in many mineral systems are, in many cases, poorly known, raising the possibility that CMs are not fully recovered from some ores. The Critical Minerals in Ores (CMiO) database, compiled by Geoscience Australia, United States Geological Survey, Geological Survey of Canada, and Geological Survey of Queensland as part of the Critical Minerals Mapping Initiative, contains high-quality geochemical data from global ore deposits classified using a common framework, enabling global comparison. Using CMiO and other data, we have undertaken preliminary investigations on distributions of CMs in mineral systems including porphyry Cu (PCu), iron oxide-Cu-Au (IOCG), iron oxide-apatite (IOA), rare earth element (REE), and Zn-dominated systems. The PCu systems are enriched in Re, Pt, Pd, Se, and Te relative to the continental crust. At the Pebble (USA) PCu deposit, Re and Se are enriched in Cu ore zones; whereas Te is enriched immediately outside these zones. Although generally not recovered, alkalic PCu deposits (e.g., Galore Creek, Canada; Cadia, Australia) can be enriched in Pd and Pt. Cobalt and some REEs occur in IOCG systems, with Co enriched in magnetite-dominant IOCG systems (e.g., Ernest Henry, Australia; Kwyjibo, Canada), and REEs enriched in IOA (e.g., Pea Ridge, USA) and hematite-dominant IOCG systems (e.g., Olympic Dam, Australia). The enrichment of individual REEs depends strongly on mineral system type. In magmatic and metasomatic systems, light REEs (Ce to Sm) and Y are enriched in hematite-rich IOCG, IOA and carbonatite (e.g., Saint-Honoré, Canada) deposits, whereas heavy REEs (Eu to Lu) are enriched in deposits associated with peralkaline magmatism (e.g., Strange Lake, Canada). Unconformity-related REE (e.g., Maw, Canada; Wolverine, Australia) and ionic clay (e.g., Koopamurra, Australia) deposits also tend to be heavy REE-rich, whereas shale-hosted (e.g., SBH, Canada) and phosphorite (e.g., Ardmore, Australia) deposits can be enriched in heavy and/or light REEs. Zinc deposits are important sources of Ga, Ge, and In. Assessment of the distribution of these CMs in Zn deposits suggest that Ge is concentrated in deposits formed from low temperature, oxidized fluids (Mississippi Valley-type: Tres Marias, Mexico; sediment-hosted massive sulfides: Red Dog, USA), whereas In is enriched in deposits formed from higher temperature, reduced fluids (volcanic-hosted massive sulfide: Kidd Creek, Canada; skarn: Isabel, Australia). These examples demonstrate the utility of the CMiO and other datasets for characterizing CMs distribution in individual ore deposit and predicting CMs potentials of mineral systems. This abstract was presented at the Joint Annual Meeting of the Geological Association of Canada (GAC), Mineralogical Association of Canada (MAC) and Society for Geology Applied to Mineral Deposits, Sudbury, Canada May 2023

This web map service provides visualisations of datasets prepared for the Technology Investment Roadmap Data Portal. The service has been developed using various mineral deposit, mine location and industrial plant location datasets sourced from the Australia’s Identified Mineral Resources (2019), produced by Geoscience Australia (http://dx.doi.org/10.11636/1327-1466.2018)

A review of mineral exploration trends, activities and discoveries in Australia in 2023.

<div>This A1 poster aims to introduce Year 3/4 and older students to the many ways that minerals and elements are used in our everyday lives. </div><div>&nbsp;6 key uses of 14 critical and strategic minerals are highlighted by colourful lines linking images. Students should take their time viewing the poster; they can follow the wiggly lines from minerals to product or vice versa and work out how many minerals link to each type of use.</div><div>&nbsp;The poster is also suitable for secondary students with the inclusion of a specific element name with each highlighted mineral plus the element symbol and atomic number.</div><div>&nbsp;The poster is intended to be a colourful rich stimulus to engage student interest in the resources from the ground used in our modern world.</div><div><br></div>

<div>High purity quartz (HPQ) is the only naturally occurring and economically viable source for the production of silicon. Silicon is a critical mineral, and a key component in modern technologies such as semiconductors and photovoltaic cells. Critical minerals support the move towards a greater reliance on electrification, renewable energy sources and economic security. The global transition to net zero carbon emissions means there is a growing need for new discoveries of HPQ to supply the silicon production chain. High purity quartz deposits are identified in a multitude of geological settings, including pegmatites, hydrothermal veins, sedimentary accumulations and quartzite; however, deposits of sufficient volume and quality are rare. Quartz is abundant throughout Australia, but the exploration and discovery of HPQ occurrences is notably under-reported, making assessment of the HPQ potential in Australia extremely difficult. This paper presents a much-needed summary of the state of the HPQ industry, exploration and deposit styles in Australia. <b>Citation:</b> Jennings, A., Senior, A., Guerin, K., Main, P., & Walsh, J. (2024). A review of high-purity quartz for silicon production in Australia. <i>Australian Journal of Earth Sciences</i>, 1–13. https://doi.org/10.1080/08120099.2024.2362296

<div>The lookbook accompanies a loan of Australian critical mineral samples provided by Geoscience Australia for display at the Australian Embassy in Washington DC, United States.&nbsp; It contains information about each of the samples, including their provenance, mineral or rock name, and the critical mineral they contain.</div>

<div>Alkaline and related rocks are a relatively rare class of igneous rocks worldwide. Alkaline rocks encompass a wide range of rock types and are mineralogically and geochemically diverse. They are typically though to have been derived by generally small to very small degrees of partial melting of a wide range of mantle compositions. As such these rocks have the potential to convey considerable information on the evolution of the Earth’s mantle (asthenosphere and lithosphere), particularly the role of metasomatism which may have been important in their generation or to which such rocks may themselves have contributed. Such rocks, by their unique compositions and or enriched source protoliths, also have considerable metallogenic potential, e.g., diamonds, Th, U, Zr, Hf, Nb, Ta, REEs. It is evident that the geographic occurrences of many of these rock types are also important, and may relate to presence of old cratons, craton margins or major lithospheric breaks. Finally, many alkaline rocks also carry with them mantle xenoliths providing a snapshot of the lithospheric mantle composition at the time of their emplacement.</div><div><br></div><div>Accordingly, although alkaline and related rocks comprise only a volumetrically minor component of the geology of Australia, they are of considerable importance to studies of lithospheric composition, evolution and architecture and to helping constrain the temporal evolution of the lithosphere, as well as more directly to metallogenesis and mineralisation.</div><div><br></div><div>This contribution presents data on the distribution and geology of Australian alkaline and related rocks of Proterozoic age. Proterozoic alkaline and related rocks are primarily restricted to the western two-thirds of the Australia continent, congruent with the distribution of Proterozoic rocks more generally. Proterozoic alkaline rock units are most abundant in Western Australia and the Northern Territory, with minor occurrences in South Australia, and the western regions of Queensland, New South Wales and Tasmania.</div><div><br></div><div>The report and accompanying GIS document the distribution, age, lithology, mineralogy and other characteristics of these rocks (e.g., extrusive/intrusive, presence of mantle xenoliths, presence of diamonds), as well as references for data sources and descriptions. The report also reviews the nomenclature of alkaline rocks and classification procedures. GIS metadata are documented in the appendices.&nbsp;</div>

The stabilities of uranyl-carbonate and uranyl-hydroxide aqueous complexes were experimentally determined at temperatures ranging from 25 to 125 °C using in situ UV–vis and Raman spectroscopic techniques. Combined with earlier determinations of the stability of chloride, sulfate, and hydroxide complexes at temperatures up to 250 °C, these data permit to create a consolidated dataset suitable for modeling of U(VI) mobilization in natural systems. The parameters of the Modified Ryzhenko-Bryzgalin and the Helgeson-Kirkham-Flowers (HKF) Equations of State (EoS) were derived based on this dataset and used for thermodynamic modeling different scenarios of U(VI) mobilization. These models suggest that at conditions relevant to natural systems, carbonate-mediated transport of U(VI) is likely suppressed by the high stability of solid UO2(OH)2 and Na2U2O7. In contrast, sulfate-mediated mobilization mechanisms are highly efficient at acidic and near-neutral pH conditions and can lead to effective hydrothermal mobilization of U(VI). <b>Citation:</b> A. Migdisov, E. Bastrakov, C. Alcorn, M. Reece, H. Boukhalfa, F.A. Capporuscio, C. Jove-Colon, A spectroscopic study of the stability of uranyl-carbonate complexes at 25–150 °C and re-visiting the data available for uranyl-chloride, uranyl-sulfate, and uranyl-hydroxide species, <i>Geochimica et Cosmochimica Acta</i>, 2024, ISSN 0016-7037, https://doi.org/10.1016/j.gca.2024.04.023.