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  • A new continental-scale geochemical atlas and dataset for Australia were officially released into the public domain at the end of June 2011. The National Geochemical Survey of Australia (NGSA) project, which started in 2007 under the Australian Government's Onshore Energy Security Program at Geoscience Australia, aimed at filling a huge knowledge gap relating to the geochemical composition of surface and near-surface materials in Australia. Better understanding the concentration levels and spatial distributions of chemical elements in the regolith has profound implications for energy and mineral exploration, as well as for natural resource management. In this world first project, a uniform regolith medium was sampled at an ultra-low density over nearly the entire continent, and subsamples from two depths and two grain-size fractions were analysed using up to three different (total, strong and weak) chemical digestions. This procedure yielded an internally consistent and comprehensive geochemical dataset for 68 chemical elements (plus additional bulk properties). From its inception, the emphasis of the project has been on quality control and documentation of procedures and results, and this has resulted in eight reports (including an atlas containing over 500 geochemical maps) and a large geochemical dataset representing the significant deliverables of this ambitious and innovative project. The NGSA project was carried out in collaboration with the geoscience agencies from every State and the Northern Territory under National Geoscience Agreements. .../...

  • ABSTRACT: Building on method developments achieved during a series of precursor pilot projects, the National Geochemical Survey of Australia (NGSA) project targets catchment outlet (overbank) sediments as a uniform sampling medium. These transported, fine-grained materials are collected (from a shallow and a deeper level) near the lowest point of 1390 catchments, which cover 91% of the country. Dry and moist Munsell® colour, soil pH and electrical conductivity and pH of 1:5 (soil:water) slurries are recorded and laser particle size analysis and infrared spectroscopy are performed. The dried samples are sieved into two grain-size fractions (<2 mm and <75 mm) that are analysed by x-ray fluorescence (XRF) and inductively-coupled mass spectrometry (ICP-MS) (multi-element, total analyses), by ICP-MS after aqua regia digestion (multi-element, including low level gold), and specialised methods for platinum group elements, fluorine and selenium. At the time of writing, 78% of the samples have been collected and most analyses are completed for the first 25% of samples. The project is due for completion in June 2011.

  • The 1:250 000 maps show the type and distribution of 51 regolith-landform units with unique dominant regolith-landform associations, and are a subset of the 205 mapping units on the six 1:100 000 maps. These units are distinct patterns of recurring landform elements with characteristic regolith associations. Geomorphic symbols indicate the location and type of geomorphic activity. The maps present a systematic analysis and interpretation of 1:89 000 scale 1973 RC9 aerial photography, 1:100 000 scale topographic maps (AUSLIG), and field mapping data. High resolution (250m line spacing) airborne gamma-ray spectrometry and magnetics (Geoterrex) were used where applicable

  • Inland sulfidic soils have recently formed throughout wetlands of the Murray River floodplain associated with increased salinity and river regulation (Lamontagne et al., 2006). Sulfides have the potential to cause widespread environmental degradation both within sulfidic soils and down stream depending on the amount of carbonate available to neutralise acidity (Dent, 1986). Sulfate reduction is facilitated by organic carbon decomposition, however, little is known about the sources of sedimentary organic carbon and carbonate or the process of sulfide accumulation within inland sulfidic wetlands. This investigation uses stable isotopes from organic carbon (13C and 15N), inorganic sulfur (34S) and carbonate (13C and 18O) to elucidate the sources and cycling of sulfur and carbon within sulfidic soils of the Loveday Disposal Basin.

  • In late 2006, the Australian Government announced its Energy Security Initiative, allowing Geoscience Australia to initiate a major program of onshore and offshore activities. The ambitious National Geochemical Survey of Australia (NGSA) project was launched in January 2007 as part of this program because until then Australia lacked a complete geochemical data coverage. Such a dataset informs on the concentrations and distributions of chemical elements in the near-surface environment. This pre-competitive knowledge, used in combination with other datasets, can contribute to making exploration for energy and mineral resources more cost-effective and less risky by helping target more detailed activities. As a spin-off, the multi-element dataset can also have applications in the fields of natural resources management, land-use decision-making and geohealth, for instance. During precursor pilot projects carried out between 2003 and 2006 in the Riverina, Gawler and Thomson regions, various sampling media, grain-size fractions and analytical methods were tested. In particular, it emerged that catchment outlet sediments from either overbank or floodplain settings or from similar low-lying settings were an ideal sampling medium that could be found across Australia. These sediments are, by their very nature, well-mixed composites of contributions from the dominant rock and soil types found within a catchment. Further, being deposited during times of receding floods, they are typically fine-grained, a beneficial property that enhances the geochemical signal-to-noise ratio. The data from the pilot projects indicated that even surface catchment outlet sediments could reflect geochemical signatures from basement and mineralisation, even when covered by thick transported overburden. .../...

  • The National Geochemical Survey of Australia (NGSA) project (www.ga.gov.au/ngsa) was part of Geoscience Australia's Onshore Energy Security Program 2006-2011 and was carried out in collaboration with the geological surveys of all States and the Northern Territory. It delivered (1) Australia's first national geochemical atlas, (2) an underpinning geochemical database, and (3) a series of reports. Catchment outlet sediments (similar to floodplain sediments in most cases) were sampled in 1186 catchments covering ~80% of the country (average sample density 1 sample per 5500 km2). Samples were collected at 2 depths each sieved to 2 grain size fractions. Chemical analyses carried out on the samples fall into 3 main categories: (1) total (using mainly XRF and total digestion ICP-MS), (2) aqua regia, and (3) Mobile Metal Ion® (MMI) element contents. The MMI analyses were conducted on the surface (0-10 cm) samples sieved to <2 mm, in one single batch, by ICP-MS. Concentrations of 54 elements (Ag, Al, As, Au, Ba, Bi, Ca, Cd, Ce, Co, Cr, Cs, Cu, Dy, Er, Eu, Fe, Ga, Gd, Hg, K, La, Li, Mg, Mn, Mo, Nb, Nd, Ni, P, Pb, Pd, Pr, Pt, Rb, Sb, Sc, Se, Sm, Sn, Sr, Ta, Tb, Te, Th, Ti, Tl, U, V, W, Y, Yb, Zn and Zr) were determined. Maps and quality assessment of these data are presented in reports available from the project website. Preliminary interpretations of the MMI dataset suggest that it potentially has significant value in geological, mineral exploration and agronomic (e.g., bioavailability) applications.