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.

<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.

Hydrochemistry data for Australian groundwater, including field and laboratory measurements of chemical parameters (electrical conductivity (EC), potential of hydrogen (pH), redox potential, and dissolved oxygen), major and minor ions, trace elements, nutrients, pesticides, isotopes and organic chemicals. < <b>Value: </b>The chemical properties of groundwater are key parameters to understand groundwater systems and their functions. Groundwater chemistry information includes the ionic and isotopic composition of the water, representing the gases and solids that are dissolved in it. Hydrochemistry data is used to understand the source, flow, and interactions of groundwater samples with surface water and geological units, providing insight into aquifer characteristics. Hydrochemistry information is key to determining the quality of groundwater resources for societal, agricultural, industrial and environmental applications. Insights from hydrochemical analyses can be used to assess a groundwater resource, the impact of land use changes, irrigation and groundwater extraction on regional groundwater quality and quantity, assess prospective mineral exploration targets, and determine how groundwater interacts with surface water in streams and lakes. <b>Scope: </b>The database was inaugurated in 2016 with hydrochemical data collected over the Australian landmass by Geoscience Australia and its predecessors, and has expanded with regional and national data. It has been in the custodianship of the hydrochemists in Geoscience Australia's Minerals, Energy and Groundwater Division and its predecessors. Explore the <b>Geoscience Australia portal - https://portal.ga.gov.au/</b>

This report contains new whole-rock and isotope geochemical data, associated sample metadata, an assessment of the data’s quality assurance, for 742 samples collected in and around the Curnamona and Delamerian provinces, across numerous drillcore sampling campaigns through 2021-23. The data can be downloaded via the Geoscience Australia EFTF portal (https://portal.ga.gov.au/persona/eftf) or in the files attached with this record (http://pid.geoscience.gov.au/dataset/ga/148651). Geochemical sampling in the Curnamona region straddles both South Australia and New South Wales. The objective of sampling was to obtain representative coverage (both stratigraphically and spatially) to support developing regional geochemical baselines (in conjunction with existing geochemistry). Thus, this sampling included both the Curnamona Province and the overlying basins (Eromanga Basin, Lake Eyre Basin). Whole-rock geochemistry is reported for 562 samples, with a subset of 13 samples analysed for Pb and Sr isotopes, and another subset of 36 samples analysed by thin section petrography (all presented herein). Geochemical sampling in the Delamerian region has focussed on available legacy drill core in South Australia, New South Wales and Victoria. The objective of sampling was to (systematically) constrain the geochemical character of magmatic rocks across the mainland extent of the Delamerian Orogen, as well as younger volcanics within the Delamerian Orogen and/or overlying cover. This geochemical sampling was conducted in conjunction with geochronology, mineral systems sampling and stratigraphic drilling (all components of the DCD project) to reinterpret the timing, character and fertility of the Delamerian Orogen. Whole-rock geochemistry is reported for 180 samples. Version 2.0 (published 28 November 2023) has added whole rock geochemistry for 22 new samples in the Delamerian region. The data products and report have been updated accordingly.

<div>Soil is a complex and spatially variable material that has a demonstrated potential to be a useful evidence class in forensic casework and intelligence operations. Here, the capability to spatially constrain searches and prioritise resources by triaging areas as low and high interest is advantageous. Conducted between 2017 and 2021, a forensically relevant topsoil survey (0-5 cm depth; 1 sample per 1 km2) has been carried out over Canberra, Australia, with the aims of documenting the distribution of chemical elements in an urban/suburban environment, and of acting as a testbed for investigating various aspects of forensic soil provenancing. Geochemical data from X-Ray Fluorescence (XRF; for total major oxides) and Inductively Coupled Plasma-Mass Spectrometry (ICP-MS; for trace elements) following a total digestion (HF + HNO3) were obtained from the survey’s 685 topsoil samples (plus 138 additional quality control samples and six “Blind” simulated evidentiary samples). Using those “Blind” samples, we document a likelihood ratio approach where for each grid cell the analytical similarity between the grid cell and evidentiary sample is attributed from a measure of overlap between both Cauchy distributions, including appropriate uncertainties. Unlike existing methods that base inclusion/exclusion on an arbitrary threshold (e.g., ± three standard deviations), our approach is free from strict binary or Boolean thresholds, providing an unconstrained gradual transition dictated by the analytical similarity. Using this provenancing model, we present and evaluate a new method for upscaling from a fine (25 m x 25 m) interpolated grid to a more appropriate coarser (500 m x 500 m) grid, in addition to an objective method using Random Match Probabilities for ranking individual variables to be used for provenancing prior to receiving evidentiary material. Our results show this collective procedure generates more consistent and robust provenance maps between two different interpolation algorithms (e.g., inverse distance weighting, and natural neighbour), grid placements (e.g., grid shifts to the north or east) and theoretical users (e.g., different computer systems, or forensic geoscientists).</div> <b>Citation:</b> Michael G. Aberle, Patrice de Caritat, James Robertson, Jurian A. Hoogewerff, A robust interpolation-based method for forensic soil provenancing: A Bayesian likelihood ratio approach,<i> Forensic Science International</i>, Volume 353, 2023, 111883, ISSN 0379-0738. https://doi.org/10.1016/j.forsciint.2023.111883.

<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)

<div>The Exploring for the Future (EFTF) program is an Australian government initiative aimed at stimulating investment in resource exploration and development. It operates multiple interconnected projects, such as the Australia’s Resources Framework (ARF), a continental-scale endeavor to enhance understanding of Australia's geology and resource potential. A module of ARF, the Geochemistry for Basin Prospectivity (G4BP), studies Australian basins with prospective base metal mineral systems. </div><div><br></div><div>The current report focuses on the Neoproterozoic segment of the Stuart Shelf region in South Australia, a part of the Adelaide Rift Complex. This research is conducted collaboratively with the Geological Survey of South Australia, examining sediment-hosted copper potential in the rift complex.</div><div><br></div><div>The Adelaide Rift Complex is a geological formation that underwent extensive sedimentation from the Neoproterozoic to early Cambrian, particularly within the rift zone. Stuart Shelf sediments overlay Mesoproterozoic magmatic and Paleoproterozoic metasediment layers. The complex hosts multiple copper deposits, which are usually associated with movement of basinal brines that leach metals from lower basinal layers or rift-related volcanic rocks.</div><div><br></div><div>To improve understanding of the geology of the Stuart Shelf and related copper mineralisation, two primary objectives were set: </div><div><br></div><div>1. Geochemical fingerprinting and baseline data collection: This involves compilation and reanalysis of existing data, along with new data collection aimed at providing comprehensive geochemical data for stratigraphic units within the Stuart Shelf.</div><div><br></div><div>2. Identification of mineral system components: Utilising data from the first objective, this phase aims to identify potential metal and fluid sources and potential sites of metal deposition. </div><div>In conjunction with these efforts, a GA-GSSA geochemical sampling project is underway, tying geochemistry to lithostratigraphic units and facies. The newly acquired geochemical data will be integrated into the overall GSSA-CSIRO project to contribute to a more comprehensive understanding of the sediment-hosted stratabound mineral system.</div><div><br></div>

Carbon Capture and Storage (CCS) is a technique for mitigating anthropogenic climate change by separating CO2 from industrial flue gas, transporting it to and storing it in a subsurface geological storage reservoir. The low-salinity (TDS<3 000 mg/L) Jurassic sandstone formations in Australia's Surat Basin have been identified as a potential reservoir system for geological CO2 sequestration. However, given the prevailing use of saline reservoirs in CCS projects elsewhere, limited data are available on CO2-water-rock dynamics during geological sequestration in such low-salinity formations. Here, a combined batch experiment and numerical modelling approach is used to characterise potential CO2-water-rock reaction pathways, to assess potential impacts of CCS on groundwater chemistry, and to identify geochemical tracers of inter- and intra-formational CO2 migration during geological sequestration within the Jurassic sandstones. Mineralogy and physical properties of the prospective reservoir are characterized for 66 core samples from stratigraphic well GSQ Chinchilla 4. Representative samples are reacted with synthetic formation water and high-purity CO2 for up to 27 days at a range of pressures to simulate conditions during carbon sequestration in the Jurassic sandstones. Results show the low formation water salinity, temperature, and mineralization in the reservoirs yield high solubility trapping capacity (1.18 mol/L at 45°C, 100 bar), while the paucity of divalent cations in groundwater and the silicate reservoir matrix result in very low mineral trapping capacity within the footprint of the supercritical CO2 (scCO2) plume. Though alkalinity buffers formation water pH under elevated CO2 pressure, the acidic pH significantly enhances mineral dissolution in reactors with heterogeneous Hutton and Boxvale Sandstone samples. Smaller TDS changes are observed for samples of the mature Precipice Sandstone than for the other formations. Non-radiogenic, regional groundwater-like 87Sr/86Sr values (0.704845 - 0.706600) in batch reactors indicate carbonate and authigenic clay dissolution as the primary reaction pathways regulating solution composition in all formations during carbon sequestration. Slightly higher Sr isotope ratios in felsic samples than in calcitic samples, and dissolved Si concentrations in mature Precipice Sandstone reactors show detrital silicate dissolution to be an ancillary process. Batch reactor degassing at the end of the incubation period was simulated to assess geochemical changes in formation waters during transport away from a scCO2 plume. Model results suggest geological sequestration in the Jurassic sandstone formations would increase regional groundwater alkalinity and redistribute carbonate minerals outside the scCO2 footprint, but is unlikely to result in net mineral trapping of CO2. Several elements are mobilised in concentrations greater than found in regional groundwater, making them viable tracers of CO2 migration. Most notable is cobalt, concentrations of which are significantly elevated regardless of CO2 pressure or sample mineralogy. Experimental results indicate manganese and cadmium concentrations may locally exceed drinking water quality guidelines, but further modelling of intra aquifer mixing is required to quantify the potential risk to regional groundwaters from trace element mobilisation.

<div>Heavy rare earth elements are essential in renewable energy and high-tech products. Some natural rare earth element (REE) deposits exhibit heavy rare earth element (HREE) enrichment from &lt;&nbsp;10% to ~85% of the REE budget (Williams-Jones et al., 2015). </div><div><br></div><div>Controls on REE fractionation in hydrothermal systems are imposed by (1) changes in the relative stability of REE aqueous complexes with temperature (Migdisov et al., 2016) and (2) incorporation or rejection of REE by crystalline structures. Also, the REEs are invariably found as solid solutions but not as pure minerals. REE and yttrium (Y) sulphate complexes are some of the most stable REE and Y aqueous species in hydrothermal fluids (Migdisov and William-Jones, 2008, 2016; Guan et al., 2022) and may be responsible for REE transport and deposition in sediment-hosted deposits. Within the unconformity-related deposits, REEs are hosted mostly by xenotime ((Y,Dy,Er,Tb,Yb)PO4) and minor florencite ((La,Ce)Al3(PO4)2(OH)6) (Nazari-Dehkordi et al., 2019). Modelling the stability of xenotime in the H-O-Cl-(±F)-S-P aqueous system is critical for understanding HREE enrichment in this mineral system.</div><div><br></div><div>We use a newly derived thermodynamic dataset depos for REESO4+ and REE(SO4)2‑ aqueous complexes to generate stability diagrams illustrating mechanisms of REE transport and deposition in the above deposits. Sulphate REE complexes may dominate even in chloride-rich brines and facilitate REE mobilization in acid oxidizing environments. Previously Nazari-Dehkordi et al. (2019) proposed an ore genesis model involving the mixing of discrete hydrothermal fluids that separately carried REE + yttrium and phosphorus. The speciation model that includes sulphate complexes expands this scenario; a process resulting in fluid neutralization or reduction will also promote precipitation of xenotime enriched in HREEs.&nbsp;</div><div><br></div>This Abstract was submitted/presented to the 2022 Specialist Group in Geochemistry, Mineralogy and Petrology (SGGMP) Conference 7-11 November (https://gsasggmp.wixsite.com/home/biennial-conference-2021)

<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>