Spectral data from airborne and ground surveys enable mapping of the mineralogy and chemistry of soils in a semi-arid terrain of Northwest Queensland. The study site is a region of low relief, 20 km southeast of Duchess near Mount Isa. The airborne hyperspectral survey identified more than twenty surface components including vegetation, ferric oxide, ferrous iron, MgOH, and white mica. Field samples were analysed by spectrometer and X-ray diffraction to test surface units defined from the airborne data. The derived surface materials map is relevant to soil mapping and mineral exploration, and also provides insights into regolith development, sediment sources, and transport pathways, all key elements of landscape evolution.

Recently, continental-scale geochemical surveys of Europe and Australia were completed. Thanks to having exchanged internal project standards prior to analysing the samples, we can demonstrate direct comparability between these datasets for 10 major oxides (Al2O3, CaO, Fe2O3, K2O, MgO, MnO, Na2O, P2O5, SiO2 and TiO2), 16 total trace elements (As, Ba, Ce, Co, Cr, Ga, Nb, Ni, Pb, Rb, Sr, Th, V, Y, Zn and Zr), 14 aqua regia extracted elements (Ag, As, Bi, Cd, Ce, Co, Cs, Cu, Fe, La, Li, Mn, Mo and Pb), Loss On Ignition (LOI) and pH. By comparing these new datasets to one another, we can learn lessons about continental-scale controls on soil geochemistry and about critical requirements for global geochemical mapping. Although the median soil compositions of both continents are overall quite similar, the Australian median values are systematically lower, except for SiO2 and Zr. This reflects the generally longer and, locally more intense weathering in Australia (median Chemical Index of Alteration values are 72 and 60% for Australia and Europe, respectively). We found that element concentrations typically span 3 (and up to 5) orders of magnitude on each continent. The comparison of 2 continental geochemical surveys shows that the most critical requirement for global geochemical mapping is good analytical quality. Only where a comprehensive quality control program, including field and laboratory duplicates, internal project standards and Certified Reference Materials, is implemented and documented, are the results credible and comparable with other datasets.

The use of airborne hyperspectral imagery for mapping soil surface mineralogy is examined for the semi-arid Tick Hill test site (20 km2) near Mount Isa in north-western Queensland. Mineral maps at 4.5 m pixel resolution include the abundances and physicochemistries (chemical composition and crystal disorder) of kaolin, illite-muscovite, and Al smectite (both montmorillonite and beidellite), as well as iron oxide, hydrated silica (opal), and soil/rock water (bound and unbound). Validation of these hyperspectral mineral maps involved field sampling (34 sites) and laboratory analyses (spectral reflectance and X-ray diffraction). The field spectral data were processed for their mineral information content the same way as the airborne HyMap data processing. The results showed significant spatial and statistical correlation. The mineral maps provide more detailed surface compositional information compared with the published soil and geology maps and other geoscience data (airborne radiometrics and digital elevation model). However, there is no apparent correlation between the published soil types (i.e. Ferrosols, Vertosols, and Tenosols) and the hyperspectral mineral maps (e.g. iron oxide-rich areas are not mapped as Ferrosols and smectite-rich areas are not mapped as Vertosols). This lack of correlation is interpreted to be related to the current lack of spatially comprehensive mineralogy for existing regional soil mapping. If correct, then this new, quantitative mineral mapping data has the potential to improve not just soil mapping but also soil and water catchment monitoring and modeling at local to regional scales. The challenges to achieving this outcome include gaining access to continental-scale hyperspectral data and models that link the surface mineralogy to subsurface soil characteristics/processes.

We describe the information content of soil visible-near infrared (vis-NIR) reflectance spectra and map their spatial distribution across Australia. The spectra of 4030 surface soil sample from across the country were measured using a vis-NIR spectrometer with a wavelength range between 350-2500 nm. The spectra were treated using a principal component analysis (PCA) and the resulting scores were mapped by ordinary point kriging. The largely dominant and common feature in the maps was the difference between the more expansive, older and more weathered landscapes in the centre and west of Australia and the generally younger, more complex landscapes in the east. A surface soil class map derived from the clustering of the principal components was similar to an existing soil classification map. We show that vis-NIR reflectance spectra: (i) provide an integrative measure to rapidly and efficiently measure the constituents of the soil, (ii) can replace the use of traditional soil properties to describe the soil and make geomorphological interpretations of its spatial distribution and (iii) can be used to classify soil objectively.

Data gathered in the field during the sample collection phase of the National Geochemical Survey of Australia (NGSA) has been used to compile the Preliminary Soil pH map of Australia. The map, which was completed in late 2009, offers a first-order estimate of where acid or alkaline soil conditions are likely to be expected. It provides fundamental datasets that can be used for mineral exploration and resource potential evaluation, environmental monitoring, landuse policy development, and geomedical studies into the health of humans, animals and plants.

Geochemical data from two continental-scale soil surveys in Europe and Australia are presented and compared. Internal project standards were exchanged to assess comparability of analytical results. The total concentration of 26 elements (Al, As, Ba, Ca, Ce, Co, Cr, Fe, Ga, K, Mg, Mn, Na, Nb, Ni, P, Pb, Rb, Si, Sr, Th, Ti, V, Y, Zn, and Zr), Loss On Ignition (LOI) and pH are found to be comparable. In addition, for the first time, directly comparable data for 14 elements in an aqua regia extraction (Ag, As, Bi, Cd, Ce, Co, Cs, Cu, Fe, La, Li, Mn, Mo, and Pb) are provided for both continents. Median soil compositions are remarkably close, though overall Australian soils are slightly depleted in all elements with the exception of SiO2 and Zr. This is interpreted to reflect the overall longer and, in places, more intense weathering in Australia. Calculation of the Chemical Index of Alteration (CIA) gives a median value of 72% for Australia compared to 60% for Europe. In general, element concentrations vary over 3 (and up to 5) orders of magnitude. Several elements (As, Ni, Co, Bi, Li, Pb, Mn, and Cu) have a lower element concentration by a factor of 2-3 in the soils of northern Europe compared to southern Europe. The break in concentration coincides with the maximum extent of the last glaciation. In Australia the central region with especially high SiO2 concentrations is commonly depleted in many elements. The data provided define the natural background variation for two continents on both hemispheres based on real data. Judging from the experience of these two continental surveys it can be concluded that analytical quality is the key requirement for the success of global geochemical mapping.

From 2007 to 2009, the National Geochemical Survey of Australia (NGSA) project collected sediment samples from 1315 sites located in 1186 catchments (~10 % of which were sampled in duplicate) from across Australia. Overbank sediments were chosen as sampling media, with a near-surface sample (Top Outlet Sediment, TOS, from 0-10 cm below the surface) and a bottom sample (Bottom Outlet Sediment, BOS, ~10 cm interval between approximately 60-80 cm below the surface) being collected. The sample sites were selected to be near outlets or spill points of large catchments, so that overbank sediments there could reasonably be assumed to represent well-mixed, fine-grained composite samples of all major rock and soil types present in the catchment. Sample sites and their corresponding sediment samples were subjected to a detailed description and the determination of bulk parameters in the field (texture, moist and dry colour, field pH). This is complemented by a series of laboratory measurements and analyses reported elsewhere. This report documents the complete field dataset and discusses the pH and soil colour data that were collected in the field. At the time of writing, field pH and colour are the only datasets available for all sites. Maps are presented showing the spatial distribution of these data in both TOS and BOS samples. These data will be the basis of further interpretative work.

The present report is a compilation of 531 geochemical maps that result from the National Geochemical Survey of Australia. These constitute the first continental-scale series of geochemical maps based on internally consistent, state-of-the-art data pertaining to the same sampling medium collected, prepared and analysed in a uniform and well documented manner and over a short time period (four years). Interpretations of the data and maps will be published separately.

Geoscience Australia and CO2CRC have constructed a greenhouse gas controlled release reference facility to simulate surface emissions of CO2 (and other GHG gases) from an underground slotted horizontal well into the atmosphere under controlled conditions. The facility is located in a paddock maintained by CSIRO Plant and Industry at Ginninderra, ACT. The design of the facility is modelled on the ZERT controlled release facility in Montana, which conducts experiments to develop capabilities and test techniques for detecting and monitoring CO2 leakage. The first phase of the installation is complete and has supported an above ground, point source, release experiment, utilising a liquid CO2 storage vessel (2.5 tonnes) with a vaporiser, mass flow controller unit with a capacity for 6 individual metered gas outlet streams, equipment shed and a gas cylinder cage. Phase 2 involved the installation of a shallow (2m depth) underground 120m horizontally drilled slotted well, in June 2011, intended to model a line source of CO2 leakage from a storage site. This presentation will detail the various activities involved in designing and installing the horizontal well, and designing a packer system to partition the well into six CO2 injection chambers. A trenchless drilling technique used for installing the slotted HDPE pipe into the bore hole will be described. The choice of well orientation based upon the effects of various factors such as topography, wind direction and ground water depth, will be discussed. It is envisaged that the facility will be ready for conducting sub-surface controlled release experiments during spring 2011.

Soil mapping at the local- (paddock), to continental-scale, may be improved through remote hyperspectral imaging of surface mineralogy. This opportunity is demonstrated for the semiarid Tick Hill test site (20 km2) near Mount Isa in western Queensland, which is part of a larger Queensland government initiative involving the public delivery of 25,000 km2 of processed airborne hyperspectral mineral maps at 4.5 m pixel resolution to the mineral exploration industry. Some of the "soil" mineral maps for the Tick Hill area include the abundances and/or physicochemistries (chemical composition and crystal disorder) of dioctahedral clays (kaolin, illite-muscovite and Al smectite, both montmorillonite and beidellite), ferric/ferrous minerals (hematite/goethite, Fe2+-bearing silicates/carbonates) and hydrated silica (opal) as well as "soil" water (bound and unbound) and green and dry (cellulose/lignin) vegetation. Validation of these hyperspectral mineral products is based on field sampling and laboratory analyses (spectral reflectance, X-ray diffraction, scanning electron microscope and electron backscatter). The mineral maps show more detailed information regards the surface composition compared with the published soil and geology (1:100,000 scale) maps and airborne radiometric imagery (collected at 200 m line spacing). This mineral information can be used to improve the published mapping but also has the potential to provide quantitative information suitable for soil modeling/monitoring.