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The colloidal transport of trace (Fe, Al, Ba, Pb, Sr, U) and ultra-trace ( 226 Ra) elements was studied in a mining environment. An original approach combining 0.45 μm filtered water sampling, the Diffusive Gradient in Thin films (DGT) technique, mineralogical characterization, and geochemical modelling was developed and tested at 17 sampling points. DGT was used for the truly dissolved fraction of the elements of interest, while the 0.45 μm filtration includes both colloidal and truly dissolved fractions (together referred to as total dissolved fraction). Results indicated a colloidal fraction for Al (up to 50%), Ba (up to 86%), and Fe (up to 99%) explained by the presence of submicrometric grains of kaolinite, barite, and ferrihydrite, respectively. Furthermore, the total dissolved 226 Ra concentration in the water samples reached up to 10-25 Bq/L (1.2-3.0 10 -12  mol/L) at 3 sampling points, while the truly dissolved aqueous 226 Ra concentrations were in the mBq/L range. Such high total dissolved concentrations are explained by retention on colloidal barite, accounting for 95% of the total dissolved 226 Ra concentration. The distribution of 226 Ra between the truly dissolved and colloidal fractions was accurately reproduced using a (Ra x ,Ba 1-x )SO 4 solid solution, with values of the Guggenheim parameter a 0 close to ideality. 226 Ra sorption on ferrihydrite and kaolinite, other minerals well known for their retention properties, could not explain the measured colloidal fractions despite their predominance. This illustrates the key role of barite in such environments. The measured concentrations of total dissolved U were very low at all the sampling points (<4.5 10 -10  mol/L) and the colloidal fraction of U accounted for less than 65%. U sorption on ferrihydrite could account for the colloidal fraction. This original approach can be applied to other trace and ultra-trace elements to complement when necessary classical environmental surveys usually performed by filtration on 0.45 μm., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Freshly erupted volcanic ash contains a range of soluble elements, some of which can generate harmful effects in living cells and are considered potentially toxic elements (PTEs). This work investigates the leaching dynamics of ash-associated PTEs in order to optimize a method for volcanic ash respiratory hazard assessment. Using three pristine (unaffected by precipitation) ash samples, we quantify the release of PTEs (Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, V, Zn) and major cations typical of ash leachates (Mg, Na, Ca, K) in multiple simulated lung fluid (SLF) preparations and under varying experimental parameters (contact time and solid to liquid ratio). Data are compared to a standard water leach (WL) to ascertain whether the WL can be used as a simple proxy for SLF leaching. The main findings are: PTE concentrations reach steady-state dissolution by 24 h, and a relatively short contact time (10 min) approximates maximum dissolution; PTE dissolution is comparatively stable at low solid to liquid ratios (1:100 to 1:1000); inclusion of commonly used macromolecules has element-specific effects, and addition of a lung surfactant has little impact on extraction efficiency. These observations indicate that a WL can be used to approximate lung bioaccessible PTEs in an eruption response situation. This is a useful step towards standardizing in vitro methods to determine the soluble-element hazard from inhaled ash., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Diffusive gradients in thin-films (DGT) is an in situ passive sampling technique to assess labile trace metal concentrations in different environmental matrix. The technique is consisting of a diffusive domain backed up by a resin gel that binds free metals and metal complexes that dissociate in the diffusive domain. This technique requires specific resin for special metals, for example mercury (Hg), since the classic resin (Chelex-100) gel is not applicable for Hg measurement. A simultaneous determination of Hg with other metals by the DGT was not yet reported. Two biomolecule-based resins were prepared by glutaraldehyde immobilisation of cysteine onto 3-amino-functionalised silica and 3-aminopropyl-functionalised silica, respectively. The load of functional groups on modified resins was qualitatively and quantitatively characterised. The modified resins were applied in the DGT technique and the uptake efficiency, elution efficiency, and linear accumulation of analytes of the DGT were tested. This novel DGT technique, using two cysteine-modified resins, can accumulate Hg and other metals in a broad range of pH and ionic strength in solutions. In the Belgian coastal zone (BCZ), the concentrations of Hg and other trace metals sampled by cysteine-modified resin-DGTs were similar as those by the other two DGT assemblies for Hg and other trace metals, respectively. The cysteine-modified silica resin combined the features of Chelex-100 resin and 3-mercaptopropyl silica resin and allowed simultaneous determination of labile Hg and other trace metals. The resin with a higher load of functional groups also showed higher performance in the further application in the DGT technique., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Digestate treatment techniques have recently been proposed as a strategy to increase the ultimate biogas yield from dairy manure and to improve the digestate quality as an organic fertilizer. These studies however rarely take the trace elements (TE) and nutrient partitioning into account. This study focusses on ozone treatment (5-40 g O 3 kg -1 Total Solids (TS)) as a digestate treatment technique to control the concentration of TE and nutrients in the liquid phase of the digestate. Controlling the TE and nutrient concentrations in the liquid and solid digestate can improve the agronomic value of dairy manure digestate. The ozone concentration of the gas stream entering reactor was 48.53 g O 3 /Nm³ or 3.4% w/w O 3 in O 2 -gas. The experiments were repeated using pure oxygen gas to investigate its influence. The results from ozonation and oxygenation of the dairy manure digestates revealed that O 3 treatment up to 40 g O 3 kg -1 TS did not have a more pronounced effect on the biochemical parameters compared to supplementation of pure O 2 . Ozonation of the digestate and the supernatant showed that the TE concentration in the liquid phase followed a parabolic profile. The observed initial increase in this parabolic profile was explained by the release of TE from the organic matter to the supernatant causing an increase in TE concentration, followed by a decrease due to precipitation of TE as hydroxides and sulfides, due to the increasing pH and sulphur concentrations., Competing Interests: Declaration of competing interest None., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Knowledge on the bioavailability of trace elements is essential in developing environmental quality standards. The purpose of this study was to explore the relationships between trace elements (in particular Uranium (U)) in sediments, porewater and their bioaccumulation by Chironomus riparius on a uranium mining site and river sediments upstream of the mine. The mobility and speciation of U in sediments was investigated using DGT. Geochemical modelling using CHESS provided insight on sorption behavior of U on ironoxyhydrite (HFO) and aqueous speciation of U. In the upstream site U concentrations found were 0.05 μmol g -1 in surface sediment, 0.84 nmol L -1 in porewater and 2.4 nmol g -1 in Chironomus riparius whereas in the ferrihydrite deposits on the mining sites the concentrations found were up to 9.4 μmol g -1 in surface sediment, 0.37 μmol L -1 in porewater and 0.684 μmol g -1 in in Chironomus riparius. Despite the large differences in concentrations of U between the two sites, sediment to dissolved partitioning coefficients, bioconcentration factor (BCF) and biota sediment accumulation factors (BSAF) were very comparable. In the upstream sediment binding of U to organic matter controls sorption and aqueous speciation of U, whereas in the HFO rich sediments, sorption on HFO and the formation of HFO colloids are the determining factors. The low BSAF factors and high BCF factors indicate that the bioaccumulation is due to uptake from the dissolved phase. The DGT probes with different binding resins provide information on the colloidal nature and lability of the dissolved U species., (Copyright © 2019. Published by Elsevier Ltd.)

Concentrations of Al, As, Bi, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, U, V and Zn were quantified in surface sediments collected from 13 different sampling sites from Cau Hai lagoon in Central Vietnam, and in 8 wild and farmed-fishes involving both pelagic and benthic species. Multivariate analysis shows that these trace elements are mainly associated with lithogenic matter, and are most likely the result of alteration and erosion processes in the lagoon. Enrichment factors and geo-accumulation indices reveal substantial sediment enrichments for both As and Bi with respect to the mean composition in the upper continental crust. As is enriched in the edible portion of fish tissue with values up to 10 times higher than the allowed limits set up by Health Canada. Target hazard quotient and target carcinogenic risk for As were assessed through fish diet and were greater than 1 and 10 -4 , respectively, indicating potential health risks for fish consumers in Cau Hai lagoon., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

In North Sea and Port Açu (Brazil) coastal areas, high arsenic (As) concentrations were observed in water, soil and sediments. Therefore, the impact of this contamination on fish and shellfish species bought from local fishermen was studied. Total As was assessed with ICP-OES (Brazil) and ICP-MS (North Sea) after microwave digestion. Toxic As was assessed with liquid chromatography-ICP-MS (Brazil) and hydride generation-atomic fluorescence spectrometry (North Sea). All analytical methods comply with Quality Assurance/Quality Control procedures. Several fish species have average Total As concentrations above 1 μg g-1 wet weight (ww), but the highest concentrations are found in less spotted dogfish, lemon sole and whelks from the North Sea, with respectively 50, 49 and 50 μg g-1 ww. High Total As concentrations correspond to high Toxic As concentrations, except for scallops having increased Toxic As concentrations. Toxic As fractions are highest in scallops (almost 10%) but rarely exceeds 2% in all other species. Liver samples were only analyzed in ray, dogfish and catfish and their Toxic As fractions are between 2 and 4 times higher than in muscle. For a consumption of 150 g of seafood, only 3 samples exceed the provisional total daily intake of 2 μg kg-1 bw, however, cancer risks are non-negligible. Using mean Toxic As concentrations for each of the different fish and shellfish species studied, Lifetime Cancer Risk values at the actual global seafood consumption rate of 54 g day-1 are above 10-4 for whelks, scallops, dogfish, ray and lemon sole., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

The Diffusive Gradients in Thin films (DGT) technique was used to analyse U, (226)Ra and other trace metals in stream water and soil porewater in a wetland in France impacted by uranium mining. High resolution profiles of metals in soil porewater obtained by DGT could be measured for the first time up to a depth of 75 cm by the construction of a novel DGT holder. In stream water, the DGT technique was compared to speciation carried out by filtration (0.45 μm) and ultrafiltration (UF) (500 kDa/100 kDa/10 kDa) and DGT porewater profiles were compared with piezometer data obtained in a parallel study. An increase in the trace concentrations of dissolved (0.45 μm) and particulate U, (226)Ra, and elements such as Al, Fe, Mn and Ba was observed in the stream water as it passes through the bog as a results of mobilization from the wetland. The porewater results indicate DGT labile metals species to be present in porewater and mobilization of uranium and other elements linked to the presence of enriched clays. In stream water, colloids and particles govern the behavior of U, Al and Fe, whereas Mn, Ba and Ra are essentially transported as truly dissolved metal species with DGT labile concentrations accounting for 100% of the dissolved fraction. The combined approaches of DGT and UF allow us to obtain a better understanding on the biogeochemical processes involved in the retention and mobility of U and (226)Ra in the wetland., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Endocrine disrupting chemicals represent a broad class of compounds, are widespread in the environment and can pose severe health effects. The objective of this study was to investigate the overall estrogen activating potential of PM10 air samples at an urban location with high traffic incidence in Flanders, using a human in vitro cell bioassay. PM10 samples (n = 36) were collected on glass fiber filters every six days between April 2013 and January 2014 using a high-volume sampler. Extraction was executed with a hexane/acetone mixture before analysis using a recombinant estrogen-responsive human ovarian carcinoma (BG1Luc4E2) cell line. In addition, several samples and procedural blanks were extracted with ultra-pure ethanol or acetonitrile to compare extraction efficiencies. Results were expressed as bioanalytical equivalents (BEQs) in femtogram 17β-estradiol equivalent (fg E2-Eq) per cubic meter of air. High fluctuations in estrogenic activity were observed during the entire sampling period, with mean and median BEQs of 50.7 and 35.9 fg E2-Eq m(-)(3), respectively. Estrogenic activity was measured in more than 70% of the samples and several sample extracts showed both high BEQs and high cytotoxicity, which could not be related to black carbon, PM10 or heavy metal concentrations. At this moment, it remains unclear which substances cause this toxicity, but comparison of results obtained with different extraction solvents indicated that acetone/hexane extracts contained more compounds that were cytotoxic and suppressive of responses than those extracted using ultra-pure ethanol. Although more research is needed, the use of a more polar extraction solvent seems to be advisable., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

PAHs, PCDD/Fs and non-ortho PCBs have been assessed in Yser and Upper-Scheldt river sediments. Higher contamination levels were observed in the Upper-Scheldt sediments: maximum concentrations for the 16 US-EPA PAHs, PCDD/Fs and non-ortho PCBs respectively amount to 8.9 mg kg(-1), 12 ng TEQ kg(-1) and 5.1 ng TEQ kg(-1). Diagnostic PAH ratios in sediments and atmospheric samples suggest that the PAH compounds are from pyrolytic origin, more specifically combustion processes. The huge consumption of coal in cokes-ovens and smelters and its use for house-heating in Northern France, although decreasing during the last decades, are in support of that suggestion. PCDD/F fingerprints in sediments and deposition material indicate that OCDD is the dominant congener. In addition use of pentachlorophenol (PCP) in the past led to a minor contribution of PCDD/Fs in our sediment samples. Non-ortho PCBs form a substantial fraction of the total TEQ concentrations observed in the sediments. Since the 1980s and 1990s a substantial reduction of the PCDD/F sediment concentrations is observed, but this is not the case for the PAHs., (Copyright © 2011 Elsevier Ltd. All rights reserved.)