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.

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.

Paleoproterozoic arc and backarc assemblages accreted to the south Laurentian margin between 1800 Ma and 1600 Ma, and previously thought to be indigenous to North America, more likely represent fragments of a dismembered marginal sea developed outboard of the formerly opposing Australian-Antarctic plate. Fugitive elements of this arc-backarc system in North America share a common geological record with their left-behind Australia-Antarctic counterparts, including discrete peaks in tectonic and/or magmatic activity at 1780 Ma, 1760 Ma, 1740 Ma, 1710-1705 Ma, 1690-1670 Ma, 1650 Ma and 1620 Ma. Subduction rollback, ocean basin closure and the arrival of Laurentia at the Australian-Antarctic convergent margin first led to arc-continent collision at 1650-1640 Ma and then continent-continent collision by 1620 Ma as the last vestiges of the backarc basin collapsed. Collision induced obduction and transfer of the arc and more outboard parts of the Australian-Antarctic backarc basin onto the Laurentian margin where they remained following later breakup of the Neoproterozoic Rodinia supercontinent. North American felsic rocks generally yield Nd depleted mantle model ages consistent with arc and backarc assemblages built on early Paleoproterozoic Australian crust as opposed to older Archean basement making up the now underlying Wyoming and Superior cratons. Appeared in Lithosphere (2019) 11 (4): 551–559, June 10, 2019.

<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.

<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.

<b>Legacy service retired 29/11/2022</b> This is an Open Geospatial Consortium (OGC) web service providing access to Australian onshore and offshore borehole data conforming to the GeoSciML version 4.0 specification. The borehole data includes Mineral Drillholes, Petroleum Wells and Water Bores along with a variety of others types. The dataset has been restricted to onshore and offshore Australian boreholes, and bores that have the potential to support geological investigations and assessment of a variety of resources.

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.

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