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.

This report presents the results of an elemental and carbon and oxygen isotope chemostratigraphy study on three historic wells; Kidson-1, Willara-1 and Samphire Marsh-1, from the southern Canning Basin, Western Australia. The objective of this study was to correlate the Early to Middle Ordovician sections of the three wells to each other and to wells with existing elemental and carbonate carbon isotope chemostratigraphy data from the Broome Platform, Kidson and Willara sub-basins, and the recently drilled and fully cored stratigraphic Waukarlycarly 1 well from the Waukarlycarly Embayment.

<div>Levelling of geochemical data between surveys is a vital step in using datasets together. This code can apply a number of approaches to eliminate inter-laboratory differences from multi-generational and spatially isolated geochemical surveys. This codes allow the use of a variety of levelling methods: re-analysis, single standards, and multiple standards. The methodology and effectiveness of each of these methods are outlined in Main, P.T. and Champion, D.C., 2022. Levelling of multi-generational and spatially isolated geochemical surveys. Journal of Geochemical Exploration.</div>

Exploring for the Future (EFTF) is an Australian Government program led by Geoscience Australia, in partnership with state and Northern Territory governments. This first phase of the EFTF program (2016–2020) aimed to assist industry investment in resource exploration in frontier regions of northern Australia by providing precompetitive data and information about energy, mineral and groundwater resource potential. As part of this initiative, this record presents whole-rock inorganic geochemistry data including X-ray fluorescence (XRF) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analyses and quantitative X-ray diffraction (qXRD) results for 67 drill core and cuttings samples of sedimentary rocks from Barnicarndy 1 drilled in the Barnicarndy Graben of the Canning Basin. The inorganic geochemistry analyses were undertaken by Geoscience Australia and Bureau Veritas (BV). This work complements other components of the EFTF program, including a comprehensive sampling program of the Barnicarndy 1 deep stratigraphic well, the Kidson Sub-basin seismic survey, and the Kidson Sub-basin petroleum systems model to better understand the geological evolution, basin architecture and petroleum prospectivity of the region.

Hydrothermal magnetite from the Starra iron oxide‑copper gold (IOCG) deposit in northwest Queensland, Australia, records a gradual decrease in V, Ni, Cr, and Mn that correlates with the transition from early, amphibole-biotite-magnetite dominant alteration to late, chlorite-quartz-hematite-dominated alteration assemblages. The observed systematic change in multivariate elements in magnetite is interpreted to indicate an increase in fO2 during the main Cu(Au) mineralization. We suggest that variations in the V, Ni, and Cr contents of magnetite at Starra indicate either a primary magmatic fluid source or the leaching of mafic rocks by fluids during early albitization. Late silician magnetite contained in ankerite veins that crosscut the pre-existing alteration assemblages in the hanging wall to the Starra 222 ore body is likely the result of a second mineralization phase, which contributed additional metals to the Starra ore bodies. Existing data on magnetite chemistry from several IOA, IOCG, Fe, and Fe-W skarn deposits show that the ratio of V to Ga discriminates the various ore types effectively. Skarn deposits are separated from IOA and IOCG by lower concentrations of V, Ni, and Cr, suggesting a more primitive fluid source or the precipitation of magnetite at distinct physicochemical conditions than IOA and IOCG deposits. Magnetite from IOA deposits exhibits a consistently elevated V concentration whereas magnetite from Fe(–– W) skarn records an increase in V concentration with the evolution of the system. A pronounced decrease in the V contents of magnetite associated with Cu Au mineralization at Starra is interpreted as a change in redox conditions from reduced to oxidized at the time of mineralization. Such variations are also observed in other IOCG deposits. We propose that systematic decreases in V concentration in magnetite during the paragenetic evolution of the host mineral system is a diagnostic indicator for Cu(Au) mineralization in IOCG deposits, and as such, it may be used as a proxy for Cu-Au exploration, if the paragenetic context of magnetite is well constrained. <b>Citation:</b> Max Hohl, Jeffrey A. Steadman, Jonathan Cloutier, Shaun L.L. Barker, Ivan Belousov, Karsten Goemann, David R. Cooke, Trace element systematics of magnetite from the Starra iron oxide‑copper gold deposits reveals early fluid conditions characteristic for Cu mineralization, <i>Chemical Geology</i>, Volume 648, 2024, 121960, ISSN 0009-2541, https://doi.org/10.1016/j.chemgeo.2024.121960

<div>Diamond exploration over the past decade has led to the discovery of a new province of kimberlitic pipes (the Webb Province) in the Gibson Desert of central Australia. The Webb pipes comprise sparse macrocrystic olivine set in a groundmass of olivine, phlogopite, perovskite, spinel, clinopyroxene, titanian-andradite and carbonate. The pipes resemble ultramafic lamprophyres (notably aillikites) in their mineralogy, major and minor oxide chemistry, and initial 87Sr/ 86Sr and <em>ε</em>Nd-<em>ε</em>Hf isotopic compositions. Ion probe U-Pb geochronology on perovskite (806 ± 22 Ma) indicates the eruption of the pipes was co-eval with plume-related magmatism within central Australia (Willouran-Gairdner Volcanic Event) associated with the opening of the Centralian Superbasin and Rodinia supercontinent break-up. The equilibration pressure and temperature of mantle-derived garnet and chromian (Cr) diopside xenocrysts range between 17 and 40 kbar and 750–1320°C and define a paleo-lithospheric thickness of 140 ± 10 km. Chemical variations of xenocrysts define litho-chemical horizons within the shallow, middle, and deep sub-continental lithospheric mantle (SCLM). The shallow SCLM (50–70 km), which includes garnet-spinel and spinel lherzolite, contains Cr diopside with weakly refertilized rare earth element compositions and unenriched compositions. The mid-lithosphere (70–85 km) has lower modal abundances of Cr diopside. This layer corresponds to a seismic mid-lithosphere discontinuity interpreted as pargasite-bearing lherzolite. The deep SCLM (&gt;90 km) comprises refertilized garnet lherzolite that was metasomatized by a silicate-carbonatite melt.</div><div><br></div><div>Geoscience Australia’s Exploring for the Future program provides precompetitive information to inform decision-making by government, community and industry on the sustainable development of Australia's mineral, energy and groundwater resources. By gathering, analysing and interpreting new and existing precompetitive geoscience data and knowledge, we are building a national picture of Australia’s geology and resource potential. This leads to a strong economy, resilient society and sustainable environment for the benefit of all Australians. This includes supporting Australia’s transition to net zero emissions, strong, sustainable resources and agriculture sectors, and economic opportunities and social benefits for Australia’s regional and remote communities. The Exploring for the Future program, which commenced in 2016, is an eight year, $225m investment by the Australian Government.</div><div><br></div><div><strong>Citation:</strong></div><div>Sudholz, Z. J., et al. (2023). Petrology, age, and rift origin of ultramafic lamprophyres (aillikites) at Mount Webb, a new alkaline province in Central Australia. <i>Geochemistry, Geophysics, Geosystems</i>, 24, e2023GC011120.</div><div>https://doi.org/10.1029/2023GC011120</div>

<div>This dataset comprises hydrochemistry results for groundwater, surface water, and rainwater samples collected as part of the Upper Darling Floodplain groundwater study. Associated methods, interpretation, and integration with other datasets are found in the Upper Darling Floodplain geological and hydrogeological assessment (Geoscience Australia Ecat ID:149689). This project is part of the Exploring for the Future (EFTF) program, an eight-year, $225 million Australian Government funded geoscience data and precompetitive information acquisition program. The dataset contains 68 groundwater samples, 17 surface water samples, and four rainwater samples. Groundwater samples are from the Cenozoic formations within the alluvium of the Darling River, the Great Artesian Basin, and the Murray geological basin. Surface water samples are from the Darling River, and rainwater samples were taken within the study area. Subsets of the samples were analysed for major ions and trace metals, stable isotopes of water (δ2H and δ18O), radiocarbon (14C), stable carbon isotopes (δ13C), strontium isotopes (87Sr/86Sr), sulfur hexafluoride (SF6), chlorofluorocarbon (CFC) isotopes, chlorine-36 (36Cl), noble gases, and Radon-222. The results were used to inform a range of hydrogeological questions including aquifer distribution and quality, inter-aquifer connectivity, and groundwater-surface water connectivity.&nbsp;</div><div><br></div>

This database contains geochemical data for samples analysed both for inorganic and organic geochemistry. Analytical data are sourced from Geoscience Australia's Inorganic Geochemistry Database (OZCHEM) and Organic Geochemistry Database (ORGCHEM), respectively. The data are joined on a unique sample number. Inorganic geochemical data cover the majority of the periodic table, with metadata on analytical methods and detection limits. Organic geochemical data include results of pyrolysis, derivative calculated values, and, where available, isotopic composition of carbonates (D13C) and isotopic composition of rock nitrogen (D15N). Further, there are provisions for delivery of isotopic data for kerogen (H, C, N) and oxygen (O) for carbonates. Where available, sample descriptions include stratigraphic unit names and ages, and lithology. Location information includes coordinates of the sampled feature (eg, borehole), coordinates of the sample and sample depth. Interpretation of the combined inorganic and organic geochemistry for organic-rich shales will facilitate comprehensive characterisation of hydrocarbons source rocks and mineral commodities source and trap environments. All are achieved within the frameworks of petroleum and mineral systems analysis. The initial data delivered by this service include 1785 samples from 35 boreholes from 14 geological provinces, including recently released data for 442 samples from the South Nicholson National Drilling Initiative Carrara 1 stratigraphic drill hole (Butcher et al., 2021; Carson et al., 2021). Many sampled boreholes are located within the polygon of the Exploring for the Future Barkly-Isa-Georgetown project. This dataset will be updated periodically as more data become available.

Brumbys 1 was an appraisal well drilled and cored through Brumbys Fault at the CO2CRC Otway International Test Centre in 2018. The Otway Project is located in South West Victoria, on private farming property approximately 35 km southeast of Warrnambool and approximately 10 km northwest of the town of Peterborough. Total measured depth was 126.6 m (80 degrees). Sonic drilling enabled excellent core recovery and the borehole was completed as a groundwater monitoring well. Brumbys 1 cores through the upper Hesse Clay, Port Campbell Limestone and extends into the Gellibrand Marl. This dataset compiles the extensive analysis undertaken on the core. Analysis includes: Core log; Foram Analysis; Paleodepth; % Carbonate (CaCO3); X-Ray Fluorescence Spectrometry (XRF); Inductively Coupled Plasma Mass Spectrometry (ICP-MS); X-Ray Diffraction (XRD); Grain Size; Density; Surface Area Analysis (SAA); Gamma. Samples were taken at approximately 1-2 m intervals.

<div>Environmental DNA (eDNA), elemental and mineralogical analyses of soil have been shown to be specific to their source material, prompting consideration of the use of dust for forensic provenancing. Dust is ubiquitous in the environment and is easily transferred to items belonging to a person of interest, making dust analysis an ideal tool in forensic casework. The advent of Next Generation Sequencing technologies means that metabarcoding of eDNA can uncover microbial, fungal, and even plant genetic fingerprints in dust particles. Combining this with elemental and mineralogical compositions offers multiple, complementary lines of evidence for tracing the origin of an unknown dust sample. This is particularly pertinent when recovering dust from a person of interest to ascertain where they may have travelled. Prior to proposing dust as a forensic trace material, however, the optimum sampling protocols and detection limits need to be established to place parameters around its utility in this context. We tested several approaches to collecting dust from different materials and determined the lowest quantity of dust that could be analysed for eDNA, geochemistry and mineralogy, whilst still yielding results capable of distinguishing between sites. We found that fungal eDNA profiles could be obtained from multiple sample types and that tape lifts were the optimum collection method for discriminating between sites. We successfully recovered both fungal and bacterial eDNA profiles down to 3&nbsp;mg of dust (the lowest tested quantity) and recovered elemental and mineralogical compositions for all tested sample quantities. We show that dust can be reliably recovered from different sample types, using different sampling techniques, and that fungal, bacterial, and elemental and mineralogical profiles, can be generated from small sample quantities, highlighting the utility of dust as a forensic provenance material.</div> <b>Citation:</b> Nicole R. Foster, Belinda Martin, Jurian Hoogewerff, Michael G. Aberle, Patrice de Caritat, Paul Roffey, Robert Edwards, Arif Malik, Priscilla Thwaites, Michelle Waycott, Jennifer Young, The utility of dust for forensic intelligence: Exploring collection methods and detection limits for environmental DNA, elemental and mineralogical analyses of dust samples, <i>Forensic Science International </i>, Volume 344, 2023, 111599, ISSN 0379-0738, https://doi.org/10.1016/j.forsciint.2023.111599. ISSN 0379-0738,