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This article presents the geochemical characteristics and physicochemical properties of water and sediment from twelve semi-permanent, dryland pools in the upper Leichhardt River catchment, north-west Queensland, Australia. The pools were examined to better understand the quality of sediments and temporary waters in a dryland system with a well-established metal contamination problem. Water and sediment sampling was conducted at the beginning of the hydroperiod in May and September 2007. Water samples were analyzed for major solute compositions (Ca, Na, K, Mg, Cl, SO(4), HCO(3)) and water-soluble (operationally defined as the <0.45 μm fraction) metals (Cd, Cu, Pb, Zn). Sediment samples were analyzed for total extractable and bioaccessible metals (As, Cd, Cu, Pb, Zn), elemental composition and grain morphology. At the time of sampling a number of pools contained water and sediment with elevated concentrations, compared to Australian regulatory guidelines, of Cu (maximum: water 28 μg L(-1); sediment 770 mg kg(-1)), Pb (maximum: water 3.4 μg L(-1); sediment 630 mg kg(-1)) and Zn (maximum: water 150 μg L(-1); sediment 780 mg kg(-1)). Concentrations of Cd and As in pools were relatively low and generally within Australian regulatory guideline values. Localized factors, such as the interaction of waters with anthropogenic contaminants from modern and historic mine wastes (i.e. residual smelter and slag materials), exert influence on the quality of pool waters. Although the pools of the upper Leichhardt River catchment are contaminated, they do not appear to be the primary repository of water and sediment associated metals when compared to materials in the remainder channel and floodplain. Nevertheless, a precautionary approach should be adopted to mitigating human exposure to contaminated environments, which might include the installation of appropriate warning signs by local health and environmental authorities.  相似文献   
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The purpose of this investigation was to determine the influence of humic acids (HA) and Ca-montmorillonite (CaM) on the solid-phase extraction (SPE) efficiency of atrazine, alachlor and α-cypermethrin from water samples at various pH-values. The nature and intensity of binding of the studied pesticides to CaM were determined by X-ray diffraction analysis and termogravimetric analysis (TGA) test. The studied pesticides eluted from discs were analysed by thin-layer chromatography (TLC). The effects of CaM and humic acid were generally pH-dependent and acted independently in extraction efficiency influence. Lower recovery of pesticides was observed at higher pH values when CaM was ≥0.1 g and was attributed to greater dispersion of clay, increased surface area and subsequent adsorption. Concentrations of dissolved organic carbon (DOC) in humic acid had less effect on the extraction efficiency when water was at pH 8 compared to water at pH 2, which was probably due to greater nonpolar interactions of the pesticides to the charge-neutralized humic acid molecule.  相似文献   
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This paper details the distribution of Cu, Pb and Zn in aquatic systems draining Mount Isa Ag-Cu-Pb-Zn Mine in arid northern Queensland, Australia. Sediment-metal concentrations in the <2mm grain-size fraction adjacent to and downstream of the mine significantly exceed background concentrations (Cu, 159; Pb, 36; Zn, 86 ppm) as well as Australian government sediment quality low trigger guidelines (Cu, 65; Pb, 50; Zn, 200 ppm). Overbank sediments are more contaminated than channel sediments with mean values of Cu, 480; Pb, 540; Zn, 750 ppm. Mean concentrations in cut riverbank samples from the <2mm fraction were Cu, 195; Pb, 724; Zn, 807 ppm. Corresponding <180 microm samples returned concentrations of Cu, 321; Pb, 995; Zn, 1110 ppm. Delivery of contaminants during wet seasons from Mount Isa Mine and historically contaminated riverbanks remains an ongoing issue. The ease of dust entrainment in arid zones means that sediments enriched in toxic concentrations of metals may be widely dispersed and ultimately ingested and absorbed by biota.  相似文献   
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