<div>Throughout geological history, marine organic-rich shales show variable but appreciable enrichment in uranium (U), < 5 to > 500 ppm. Here we report the results of high-energy resolution fluorescence detection (HERFD) x-ray absorption spectroscopy at U L3 and M4 edges to characterize U speciation in marine sediments.</div><div><br></div><div>We characterised U oxidation state in samples from the Cretaceous Toolebuc Formation of the Eromanga Basin, Australia. Nine samples were carbonaceous shales with high total organic carbon (TOC) content of 5.9 to 13.4 wt&nbsp;% and with low maturity organic matter. Two samples of coquinite were selected for comparison (TOC 0.3 and 2.4 wt %).</div><div><br></div><div>Our results suggest that a significant proportion of U in marine black shales (~20 to 30%) exists as U(VI) (Figures 1-2), despite the extremely reducing (anoxic to euxinic) conditions during sediment precipitation and diagenesis. Within individual samples, spot analyses indicate variation in the estimated oxidation state within a range of ~20% of U(VI). Uranium is unevenly distributed at mm to nanoscale. Nanoscale secondary ion mass spectrometry (NanoSIMS) reveals different associations that often coexist in single samples; nano-particulate uranium is associated with organic matter matrix or sulphide minerals, whereas phosphate minerals display diffuse uranium enrichment. The coquinite has a higher proportion of U(VI), consistent with the dysoxic depositional environment (Boreham and Powell, 1987).</div><div><br></div><div>The unexpectedly enhanced proportion of U(VI) relative to U(IV) within marine organic-rich shales implies that U might not be immediately fixed by reduction processes during sedimentation, but adsorbed by accumulating organic matter, at least in part as U(VI). This is consistent with the behaviour of uranium reported within the water column of the anoxic Black Sea (Anderson, 1989), experiments on U(VI) sorption by organic matter (e.g., Bhat et al., 2008), and previously documented redox state of U from continental organic-rich Eocene (56-34 Ma) sediments of paleochannel and lacustrine origin (Cumberland et al., 2018).</div><div><br></div><div>The results are significant for improving hydrocarbon exploration in known fields (covering the gap to a carbon-free economy without development of new greenfield oil provinces); economic geology (uranium, base-metal, and critical-metal deposits); and environmental management (evaluating potential mobilization of U by groundwaters).</div><div><br></div>This Abstract was submitted and presented to the 2023 Goldschmidt Conference Lyon, France (https://conf.goldschmidt.info/goldschmidt/2023/meetingapp.cgi)

A comprehensive geochemical program was carried out on rock samples collected in the NDI Carrara 1 drill hole, the first stratigraphic test of the newly discovered Carrara Sub-basin located in the South Nicholson region of northern Australia. The drill hole recovered continuous core from 284 m to total depth at 1750 m and intersected approximately 1120 m of Proterozoic sedimentary rocks, unconformably overlain by 630 m of Cambrian Georgina Basin carbonate-rich rocks. Total organic carbon (TOC) contents from Rock-Eval pyrolysis highlight the potential for several thick black shales to be a source of petroleum for conventional and unconventional plays. Cambrian rocks contain an organic-rich section with TOC contents of up to 4.7 wt.% and excellent oil-generating potential. The Proterozoic section is overmature for oil generation but mature for gas generation, with potential for generating gas in carbonaceous mudstones showing TOC contents up to 5.5 wt.% between 680 and 725 m depth. A sustained release of methane (up to 2%) recorded during drilling from 1150 to 1500 m suggests potential for an unconventional gas system in the Proterozoic rocks from 950 to 1415 m depth, which exhibit favourable organic richness and thermal maturity. The Proterozoic rocks, which are comparable in age to the sediment-hosted deposits of the Century Mine, contain local occurrences of lead, zinc and copper sulfide minerals providing hints of mineralisation. The combined geochemical results offer the promise of a potential new resource province in northern Australia. <b>Citation:</b> E. Grosjean, A.J.M. Jarrett, C.J. Boreham, L. Wang, L. Johnson, J.M. Hope, P. Ranasinghe, J.J. Brocks, A.H.E. Bailey, G.A. Butcher, C.J. Carson, Resource potential of the Proterozoic–Paleozoic Carrara depocentre, South Nicholson region, Australia: Insights from stratigraphic drilling, <i>Organic Geochemistry</i>, Volume 186, 2023, 104688, ISSN 0146-6380, DOI: https://doi.org/10.1016/j.orggeochem.2023.104688.

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>Geochemistry of soils, stream sediments, and overbank sediments, plays an important part in informing geochemical environmental baselines, mineral prospectivity, and environmental management practices. Australia has a large number of such surveys, but they are spatially isolated and often used in isolation. First released in 2020, the Levelled Geochemical Baseline of Australia focused on levelling such surveys across the North Australian Craton, so that they could be used as a seamless dataset. This data release acts as an update to the Levelled Geochemical Baseline of Australia by changing the focus to national scale and incorporating recently reanalysed legacy samples.</div><div><br></div><div>This work was undertaken as part of the Exploring for the Future program, an eight-year program by the Australian government. The 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, was an eight year, $225m investment by the Australian Government.</div><div><br></div><div><br></div><div><br></div><div><br></div>

Geoscience Australia and its predecessors have analysed hydrochemistry of water sampled from boreholes (both pore water and groundwater), surface features, and rainwater. Sampling was undertaken during drilling or monitoring projects, and this dataset represents a significant subset of stored analyses. Water chemistry including isotopic data is essential to better understand groundwater origins, ages and dynamics, processes such as recharge and inter-aquifer connectivity and for informing conceptual and numerical groundwater models. This GA dataset underpins a nationally consistent data delivery tool and web-based mapping to visualise, analyse and download groundwater chemistry and environmental isotope data. This dataset is a spatially-enabled groundwater hydrochemistry database based on hydrochemistry data from projects completed in Geoscience Australia. The database includes information on physical-chemical parameters (EC, pH, redox potential, dissolved oxygen), major and minor ions, trace elements, nutrients, pesticides, isotopes and organic chemicals. Basic calculations for piper plots colours are derived from Peeters, 2013 - A Background Color Scheme for Piper Plots to Spatially Visualize Hydrochemical Patterns - Groundwater, Volume 52(1) <https://doi.org/10.1111/gwat.12118>. Upon loading the data to the database, all hydrochemistry data are assessed for reliability using Quality Assurance/Quality Control procedures and all datasets were standardised. This data is made accessible with open geospatial consortium (OGC) web services and is discoverable via the Geoscience Australia Portal (<a href="https://portal.ga.gov.au/">https://portal.ga.gov.au/</a>). This dataset is published with the permission of the CEO, Geoscience Australia.

The Paleo- to Mesoproterozoic McArthur Basin and Mount Isa region of northern Australia (Figure 1) is richly-endowed with a range of deposit types (e.g., Ahmad et al., 2013; Geological Survey of Queensland, 2011). These include the basin-hosted base metal (Zn-Pb-Ag) deposits of the North Australian Zinc Belt, the richest zinc province in the world (Geological Survey of Queensland, 2011; Huston et al., 2006), as well as Cu (e.g., Mt Isa Copper) and IOCG (e.g., Ernest Henry) deposits (Geological Survey of Queensland, 2011). The giant size of the base metal deposits makes them attractive exploration targets and significant effort has been undertaken in understanding their genesis and setting and developing methodologies and data sets to aid in further discovery. As part of its Exploring for the Future program, Geoscience Australia is acquiring new, and reprocessing old, data sets to provide industry with new exploration tools for these basin-hosted Zn-Pb and Cu deposits, as well as iron-oxide copper-gold deposits. We have adopted a mineral systems approach (e.g., Huston et al., 2016) focussing on regional aspects such as source rocks, locations of mineral deposits, mineralisation haloes and footprints. Increased understanding of these aspects requires knowledge of the background variability of unaltered rocks within the basin. To assist in this we have undertaken a campaign of baseline geochemical studies, with over 800 new samples collected from sedimentary and igneous units of selected parts of the greater McArthur Basin–Mount Isa region. This has allowed us to document temporal and regional background geochemical (and mineralogical) variation within, and between sedimentary and igneous units. The main focus of this work was directed towards aspects of base metal mineralisation; a concurrent GA study (e.g., Jarrett et al., 2019) looking at aspects of hydrocarbon potential was undertaken in parallel. Appeared in Annual Geoscience Exploration Seminar (AGES) Proceedings, Alice Springs, Northern Territory 24-25 March 2020, p. 105

<b>IMPORTANT NOTICE: </b>This web service has been deprecated. The Australian Onshore and Offshore Boreholes OGC service at https://services.ga.gov.au/gis/boreholes/ows should now be used for accessing Geoscience Australia borehole data. This is an Open Geospatial Consortium (OGC) web service providing access to a subset of Australian geoscience samples data held by Geoscience Australia. The subset currently relates specifically to Australian Boreholes.

<b>IMPORTANT NOTICE:</b> This web service has been deprecated. The Australian Onshore and Offshore Boreholes OGC service at https://services.ga.gov.au/gis/boreholes/ows should now be used for accessing Geoscience Australia borehole data. This is an Open Geospatial Consortium (OGC) web service providing access to a subset of Australian geoscience samples data held by Geoscience Australia. The subset currently relates specifically to Australian Boreholes.

Manuscript detailing the results of chlorite dissolution experiments conducted at Geoscience Australia.

<b>IMPORTANT NOTICE:</b> This web service has been deprecated. The Hydrochemistry Service OGC service at https://services.ga.gov.au/gis/hydrogeochemistry/ows should now be used for accessing Geoscience Australia hydrochemistry analyses data. This is an Open Geospatial Consortium (OGC) web service providing access to hydrochemistry data (groundwater analyses) obtained from water samples collected from Australian water bores.