390 research outputs found

    Continental-scale geochemical surveys and mineral prospectivity: Comparison of a trivariate and a multivariate approach

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    The National Geochemical Survey of Australia (NGSA) provides an internally consistent, state-of-the-art, continental-scale geochemical dataset that can be used to assess areas of Australia more elevated in commodity metals and/or pathfinder elements than others. But do regions elevated in such elements correspond to known mineralized provinces, and what is the best method for detecting and thus potentially predicting those? Here, using base metal associations as an example, I compare a trivariate rank-based index and a multivariate-based Principal Component Analysis method. The analysis suggests that the simpler rank-based index better discriminates catchments endowed with known base metal mineralization from barren ones and could be used as a first-pass prospectivity tool

    An improved method for assessing the degree of geochemical similarity (DOGS2) between samples from multi-element geochemical datasets

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    The multi-element aqua regia National Geochemical Survey of Australia (NGSA) database is used to demonstrate an improved method for quantifying the degree of geochemical similarity (DOGS2) between soil samples. The improvements introduced here address issues relating to compositional data (closure, relative scale). After removing the elements with excessive censored (below detection) values, the rank-based Spearman correlation coefficient (rs) between samples is calculated for the remaining 51 elements. Each element is given equal weight through the rank-based correlation. The rs values for pairs of samples of known similar origin (e.g. granitoid-derived) are significantly positive, whereas they are significantly negative for pairs of samples of known dissimilar origin (e.g. granitoid- v. greenstone-derived). Maps of rs for all samples in the database against various reference samples are used to obtain correlation maps for lithological derivations. Likewise, the distribution of soils having a geochemical fingerprint similar to established mineralized provinces can be mapped, providing a simple, first order mineral prospectivity tool. Sensitivity of results to the removal of up to a dozen elements from the correlation indicates the method to be extremely robust. The new method is compliant with contemporary compositional data analysis principles and is applicable to various digestion methods.The NGSA project was part of the Australian Government’s Onshore Energy Security Program 2006–2011, from which funding support is gratefully acknowledged

    Establishing geochemical background variation and threshold values for 59 elements in Australian surface soil

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    During the National Geochemical Survey of Australia over 1300 top (0–10 cm depth) and bottom (~ 60–80 cm depth) sediment samples (including ~ 10% field duplicates) were collected from the outlet of 1186 catchments covering 81% of the continent at an average sample density of 1 site/5200 km2. The < 2 mm fraction of these samples was analysed for 59 elements by ICP-MS following an aqua regia digestion. Results are used here to establish the geochemical background variation of these elements, including potentially toxic elements (PTEs), in Australian surface soil. Different methods of obtaining geochemical threshold values, which differentiate between background and those samples with unusually high element concentrations and requiring attention, are presented and compared to Western Australia's ‘ecological investigation levels’ (EILs) established for 14 PTEs. For Mn and V these EILs are so low that an unrealistically large proportion (~ 24%) of the sampled sites would need investigation in Australia. For the 12 remaining elements (As, Ba, Cd, Co, Cr, Cu, Hg, Mo, Ni, Pb, Sn and Zn) few sample sites require investigation and as most of these are located far from human activity centres, they potentially suggest either minor local contamination or mineral exploration potential rather than pollution. No major diffuse source of contamination by PTEs affects Australian soil at the continental scale. Of the statistical methods used to establish geochemical threshold values, the most pertinent results come from identifying breaks in cumulative probability distributions, the Tukey inner fence and the 98th percentile. Geochemical threshold values for 59 elements, including emerging ‘high-tech’ critical elements such as lanthanides, Be, Ga or Ge, for which no EILs currently exist, are presented

    Preference fusion and Condorcet's Paradox under uncertainty

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    Facing an unknown situation, a person may not be able to firmly elicit his/her preferences over different alternatives, so he/she tends to express uncertain preferences. Given a community of different persons expressing their preferences over certain alternatives under uncertainty, to get a collective representative opinion of the whole community, a preference fusion process is required. The aim of this work is to propose a preference fusion method that copes with uncertainty and escape from the Condorcet paradox. To model preferences under uncertainty, we propose to develop a model of preferences based on belief function theory that accurately describes and captures the uncertainty associated with individual or collective preferences. This work improves and extends the previous results. This work improves and extends the contribution presented in a previous work. The benefits of our contribution are twofold. On the one hand, we propose a qualitative and expressive preference modeling strategy based on belief-function theory which scales better with the number of sources. On the other hand, we propose an incremental distance-based algorithm (using Jousselme distance) for the construction of the collective preference order to avoid the Condorcet Paradox.Comment: International Conference on Information Fusion, Jul 2017, Xi'an, Chin

    Publicly available datasets on thallium (Tl) in the environment-a comment on "Presence of thallium in the environment: sources of contaminations, distribution and monitoring methods" by Bozena Karbowska, Environ Monit Assess (2016) 188: 640 (DOI 10.1007/s10661-016-5647-y)

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    This comment highlights a whole series of datasets on thallium concentrations in the environment that were overlooked in the recent review by Karbowska, Environmental Monitoring and Assessment, 188, 640, 2016 in this journal. Geochemical surveys carried out over the last few decades all over the world at various scales and using different sampling media have reported the concentration of thallium (and dozens more elements) in tens of thousands of samples. These datasets provide a `real-world' foundation upon which source apportionment investigations can be based, monitoring programs devised and modelling studies designed. Furthermore, this comment also draws attention to two global geochemical mapping initiatives that should be of interest to environmental scientists

    Catchment-based gold prospectivity analysis combining geochemical, geophysical and geological data across northern Australia

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    The results of a pilot study into the application of an unsupervised clustering approach to the analysis of catchment-based National Geochemical Survey of Australia (NGSA) geochemical data combined with geophysical and geological data across northern Australia are documented. NGSA Mobile Metal Ion (R) (MMI) element concentrations and first and second order statistical summaries across catchments of geophysical data and geological data are integrated and analysed using Self-Organizing Maps (SOM). Input features that contribute significantly to the separation of catchment clusters are objectively identified and assessed. A case study of the application of SOM for assessing the spatial relationships between Au mines and mineral occurrences in catchment clusters is presented. Catchments with high mean Au code-vector concentrations are found downstream of areas known to host Au mineralization. This knowledge is used to identify upstream catchments exhibiting geophysical and geological features that indicate likely Au mineralization. The approach documented here suggests that catchment-based geochemical data and summaries of geophysical and geological data can be combined to highlight areas that potentially host previously unrecognised Au mineralization.The NGSA project was part of the Australian Government’s Onshore Energy Security Program 2006 – 2011, from which funding support is gratefully acknowledged

    Quantifying Diffuse Contamination: Method and Application to Pb in Soil

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    A new method for detecting and quantifying diffuse contamination at the continental to regional scale is based on the, analysis of cumulative,distribution functions (CDFs). It uses cumulative probability (CP) plots for spatially representative data sets, preferably containing >1000 determinations. Simulations demonstrate how different types of contamination influence elemental CDFs of different sample media. It is found that diffuse contamination is characterized by a distinctive shift of the low-concentration end of the distribution of the studied element in its CP plot. Diffuse contamination can be detected and quantified via either (1) comparing the distribution of the contaminating element to that of an element with a geochemically comparable behavior but no contamination source (e.g., Pb vs Rb), or (2) comparing the top soil distribution of an element to the distribution of the same element in subsoil samples from the same area, taking soil forming processes into consideration. Both procedures are demonstrated for geochemical soil data sets from Europe, Australia, and the U.S.A. Several different data sets from Europe deliver comparable results at different scales. Diffuse Pb contamination in surface soil is estimated to be <0.5 mg/kg for Australia, 1-3 mg/kg for Europe, and 1-2 mg/kg, or at least <5 mg/kg, for the U.S.A. The analysis presented here also allows recognition of local contamination sources and can be used to efficiently monitor diffuse contamination at the continental to regional scale

    Chemical elements in the environment: Multi-element geochemical datasets from continental- to national-scale surveys on four continents

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    During the last 10–20 years, Geological Surveys around the world have undertaken a major effort towards delivering fully harmonised and tightly quality controlled low-density multi-element soil geochemical maps and datasets of vast regions including up to whole continents. Concentrations of between 45 and 60 elements commonly have been determined in a variety of different regolith types (e.g., sediment, soil). The multi-element datasets are published as complete geochemical atlases and made available to the general public. Several other geochemical datasets covering smaller areas, but generally at a higher spatial density, are also available. These datasets may, however, not be found by superficial internet-based searches because the elements are not mentioned individually either in the title or in the keyword lists of the original references. This publication attempts to increase the visibility and discoverability of these fundamental background datasets covering large areas up to whole continents.We thank the governments and other sponsors for funding geochemical surveys, field and laboratory support teams and collaborators for their support, and land owners for granting access to field sites around the globe

    Using surface regolith geochemistry to map the major crustal blocks of the Australian continent

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    Multi-element near-surface geochemistry from the National Geochemical Survey of Australia has been evaluated in the context of mapping the exposed to deeply buried major crustal blocks of the Australian continent. The major crustal blocks, interpreted from geophysical and geological data, reflect distinct tectonic domains comprised of early Archean to recent Cenozoic igneous, metamorphic and sedimentary rock assemblages. The geochemical data have been treated as compositional data to uniquely describe and characterize the geochemistry of the regolith overlying the major crustal blocks across Australia according to the following workflow: imputation of missing/censored data, log-ratio transformation, multivariate statistical analysis, multivariate geospatial (minimum/maximum autocorrelation factor) analysis, and classification. Using cross validation techniques, the uniqueness of each major crustal block has been quantified. The ability to predict the membership of a surface regolith sample to one or more of the major crustal blocks is demonstrated. The predicted crustal block assignments define spatially coherent regions that coincide with the known crustal blocks. In some areas, inaccurate predictions are due to uncertainty in the initial crustal boundary definition or from surficial processes that mask the crustal block geochemical signature. In conclusion, the geochemical composition of the Australian surface regolith generally can be used to map the underlying crustal architecture, despite secondary modifications due to physical transport and chemical weathering effects. This methodology is however less effective where extensive and thick sedimentary basins such as the Eromanga and Eucla basins overlie crustal blocks
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