Polybromodiphenyl Ethers Research Articles

Novel brominated flame retardants relevant for European aquatic environments: ranking of analytes to monitor and focus on the French Eastern Mediterranean coastline.

Around a hundred of novel brominated flame retardants are currently being used to replace those regulated in the 2000s. However, data about their production, usage, and toxicity is still scarce, as well as their levels of contamination in the Mediterranean Sea and the subsequent risk. Our goal was to select the relevant novel brominated flame retardants to monitor and to apply it along the northeastern Mediterranean Sea. We proposed a ranking for novel brominated flame retardants based on their production or import, occurrence, and ecotoxicology, yielding to a selection of 21 priority molecules. From this list, 16 compounds were analyzed in ten coastal suspended matter samples, together with six related chemicals. To assess their occurrence in comparison to better documented flame retardants, eight legacy polybromodiphenyl ethers, seven polychlorobiphenyls, and short- and medium-chain chlorinated paraffins were also targeted. Novel brominated flame retardants and polychlorobiphenyls were detected in all the samples. Polybromodiphenyl ethers and chlorinated paraffins were detected in nine and seven samples, respectively. Out of the 22 novel brominated flame retardants analyzed, nine were detected, with total concentrations ranging from 0.4 to 18.5ng.g-1 d.w., which was often higher than that of polybromodiphenyl ethers. A high risk for 2,4,6‑tribromophenol and PCB118 was assessed in two and six samples, respectively. To our knowledge, this is the first priority ranking and screening of most of the novel brominated flame retardants selected in the French Mediterranean Sea.

Co-transport of polybromodiphenyl ethers and soil nanoparticles in saturated porous media: implications for the risks of polybromodiphenyl ether spreading in groundwater

This study demonstrates that PBDEs attached to soil nanoparticles can be highly mobile in saturated porous media, providing important insights on risk assessment of PBDEs contamination.

Soil colloids can significantly enhance spreading of polybromodiphenyl ethers in groundwater by serving as an effective carrier

Polybromodiphenyl ethers (PBDEs), the widely used flame retardants, are common contaminants in surface soils at e-waste recycling sites. The association of PBDEs with soil colloids has been observed, indicating the potential risk to groundwater due to colloid-facilitated transport. However, the extent to which soil colloids may enhance the spreading of PBDEs in groundwater is largely unknown. Herein, we report the co-transport of decabromodiphenyl ester (BDE-209) and soil colloids in saturated porous media. The colloids released from a soil sample collected at an e-waste recycling site in Tianjin, China, contain high concentration of PBDEs, with BDE-209 being the most abundant conger (320 ± 30 mg/kg). The colloids exhibit relatively high mobility in saturated sand columns, under conditions commonly observed in groundwater environments. Notably, under all the tested conditions (i.e., varying flow velocity, pH, ionic species and ionic strength), the mass of eluted BDE-209 correlates linearly with that of eluted soil colloids, even though the mobility of the colloids varies markedly depending on the specific hydrodynamic and solution chemistry conditions involved. Additionally, the mass of BDE-209 retained in the columns also correlates strongly with the mass of retained colloids. Apparently, the PBDEs remain bound to soil colloids during transport in porous media. Findings in this study indicate that soil colloids may significantly promote the transport of PBDEs in groundwater by serving as an effective carrier. This might be the reason why the highly insoluble and adsorptive PBDEs are found in groundwater at some PBDE-contaminated sites.

Linking Transthyretin-Binding Chemicals and Free Thyroid Hormones: In Vitro to In Vivo Extrapolation Based on a Competitive Binding Model.

Large numbers of pollutants competitively inhibit the binding between thyroid hormones and transthyretin (TTR) in vitro. However, the impact of this unintended binding on free thyroid hormones in vivo has not yet been characterized. Herein, we established a quantitative in vitro to in vivo extrapolation (QIVIVE) method based on a competitive binding model to quantify the effect of TTR-binding chemicals on free thyroid hormones in human blood. Twenty-five TTR-binding chemicals including 6 hydroxyl polybromodiphenyl ethers (OH-PDBEs), 6 hydroxyl polychlorobiphenyls (OH-PCBs), 4 halogenphenols, 5 per- and polyfluorinated substances (PFASs), and 4 phenols were selected for investigation. Incorporating the in vitro binding parameters and human exposure data, the QIVIVE model could well predict the in vivo effect on free thyroid hormones. Co-exposure to twenty-five typical TTR-binding chemicals resulted in median increases of 0.080 and 0.060% in circulating levels of free thyroxine (FT4) and free triiodothyronine (FT3) in the general population. Individuals with occupational exposure to TTR-binding chemicals suffered 1.88-32.2% increases in free thyroid hormone levels. This study provides a quantitative tool to evaluate the thyroid-disrupting risks of TTR-binding chemicals and proposes a new framework for assessing the in vivo effects of chemical exposures on endogenous molecules.

PERSISTENT ORGANIC POLLUTANTS IN BELARUS: SOURCES, STOCKPILES, REGULATION

The article is devoted to the results of the study in Belarus of the chemicals, additionally included in the Stockholm Convention on Persistent Organic Pollutants (POPs) – ‘new’ POPs. The features of ‘new’ POPs and the problems of their identification are shown. The situation with industrial chemicals based on ‘new’ POPs in Belarus,
 including polybromodiphenyl esters, per- and polyfluorinated compounds, short-chain chlorinated paraffins, polychlorinated
 naphthalenes and other POPs is briefly described. Estimates of technogenic flows of polybromodiphenyl ethers in the composition of polymer waste of electrical and electronic equipment, including the volume of their annual formation
 on the territory of Belarus, are given. The list of scientific and methodological and regulatory technical documents for
 the regulation of POPs in Belarus, developed as part of the implementation of a number of activities of State scientific
 and technical programs, National plans and subprograms on the management of POPs, is given. Priority measures for
 the environmentally sound management of POPs, additionally included in the Convention, as well as the main directions
 of further research are identified.

Presence of novel and legacy flame retardants and other pollutants in an e-waste site in China and associated risks

Electrical and Electronic Equipment (EEE) residues and their management have been widely identified as potential sources of plasticizers and flame retardants to the environment, especially in non-formal e-waste facilities. This study evaluates the distribution, partitioning and environmental and human impact of organophosphate esters (OPEs), legacy polychlorinated biphenyls (PCBs), polybromodiphenyl ethers (PBDEs) and organochlorine pesticides (OCPs) in the e-waste recycling area of Baihe Tang village, in the Qingyuan county, Guangdong province, China. A plastic debris lump accumulated in a small pond during years was identified as the main source of pollution with ∑pollutants of 8400 μg/g dw, being OPEs the main contaminants detected, followed by PBDEs. This lump produced the contamination of water, sediments, soils and hen eggs in the surrounding area at high concentrations. Plastic-water and water-sediment partitioning coefficients explained the migration of OPEs to the water body and accumulation in sediments, with a strong dependence according to the KOW. Triphenyl phosphate (TPhP), tricresyl phosphate (TCPs) and high chlorination degree PCBs produced a risk in soils and sediments, considering the lowest predicted no effect concentration, while the presence of PCBs and PBDEs in free range hen eggs exceeded the acceptable daily intake. OCPs were detected at low concentrations in all samples. The presence of organic contaminants in e-waste facilities worldwide is discussed to highlight the need for a strict control of EEE management to minimize environmental and human risks.

Impact of mixtures of persistent organic pollutants on breast cancer aggressiveness

IntroductionBreast cancer (BC) is frequent with a poor prognosis in case of metastasis. The role of the environment has been poorly evaluated in its progression. We searched to assess whether a mixture of pollutants could be responsible of BC aggressiveness. MethodsPatients undergoing surgery for their BC were prospectively included in the METAPOP cohort. Forty-two POPs were extracted, among them 17 dioxins (PCDD/F), 16 polychlorobiphenyls (PCB), 8 polybromodiphenylethers (PBDE) and 2,2′,4,4′,5,5′-hexabromobiphenyl (PBB153) were measured in the adipose tissue surrounding the tumor. BC aggressiveness was defined using tumor size and metastasis (distant or lymph nodes). Two complementary models were used to evaluate the impact of the mixture of pollutants: the BKMR (Bayesian Kernel machine regression) and WQS (weighted quantile sum regression) models. The WQS estimates the weight (positive or negative) of a certain chemical based on its quantile and the BKMR model applies a kernel-based approach to estimate posterior inclusion probabilities. The sub-group of patients with a body mass index (BMI) > 22 kg/ m2 was also analyzed. ResultsNinety-one patients were included. Of these, 38 patients presented a metastasis, and the mean tumor size was 25.4 mm. The mean BMI was 24.5 kg/m2 (+/- 4.1). No statistical association was found in the general population. However, in patients with a BMI > 22 kg/ m2, our mixture was positively associated with tumor size (OR: 9.73 95 %CI: 1.30–18.15) and metastasis (OR = 3.98 95 %CI = 1.09–17.53) using the WQS model. Moreover, using the BKMR model on chemical families, dioxin like chemicals and PCDD were associated with a higher risk of metastasis. DiscussionThese novel findings identified a mixture associated with breast cancer aggressiveness in patients with a BMI > 22 kg/ m2.

Metal-organic frameworks incorporated with C3N4: A visible light enhanced platform for degradation of polybromodiphenyl ethers

A series of nano-photocatalysts metal-organic frameworks (MOFs)/graphitic carbon nitride (CN) (named MOFCN-x) with high activity have been synthesized by in-situ growth method. Under visible light irradiation, MOFCN-x hybrids show enhanced photocatalytic activity for the debromination of polybromodiphenyl ethers (PBDEs) compared with CN. Among all the hybrids, MOFCN-2 shows the highest reaction rate, which is 3.3 times as high as that in CN. MOFCN-x photocatalysts own stable visible light activity after recycled experiment. It indicates that a moderate amount of MOFs in MOFCN-x can largely enhance the photocatalytic ability by improved visible light absorption, larger specific surface area and better photo-generated charge carriers separation and transfer capabilities. More interestingly, the debromination pathway of PBDEs by MOFCN-x shows obvious selectivity compared with pure CN that bromines at meta-positions are much more susceptible than those at the para- and ortho-positions. The possible photoreductive mechanism has been proposed. This study shows that nanocomposite MOFCN can be an excellent candidate for dealing with halogen pollutants by solar-driven.

Seabird-mediated transport of organohalogen compounds to remote sites (North West Greenland polynya)

The role of sea birds as carriers of pollutants over long distances was evaluated by analyzing organochlorine and organobromine compounds in lake sediment cores from three remote sites around the North Water polynya (North West Greenland). One lake, NOW5, was in the vicinity of a little auk (Alle alle L.) bird colony, whereas the other two lakes, NOW14 and Q5, were undisturbed by seabirds. The former was strongly acidic (pH = 3.4) but the latter had a pH close to 8. Due to the guano loading, NOW5 exhibited higher chlorophyll concentrations (74 μg/L) than the other two lakes (1.6–3.4 μg/L), higher content of total phosphorous (0.34 mg/L vs. 0.007–0.01 mg/L) and total nitrogen (3.75 mg/L vs. 0.21–0.75 mg/L).The concentrations of all organohalogen compounds were substantially greater in NOW5 than in the other lakes, indicating the strong influence of these seabirds in the transport and deposition of these compounds to remote sites. However, not all compounds showed the same increases. Hexachlorocyclohexanes and endosulfans were more than 18 times higher in NOW5, the drin pesticides and hexachlorobenzene (HCB), between 9.5 and 18 times and DDTs, polybromodiphenyl ethers (PBDEs), polychlorobiphenyls (PCBs) and chlordanes about 2.7–6 times. These differences demonstrated that the bird-mediated deposition has preservation effects of the less stable and more volatile compounds, e.g. those with log Kaw < −2.4, log Koa < 9 and/or log Kow < 6.8.The sedimentary fluxes of PCBs, HCHs, drins, chlordanes, PBDEs, HCB and endosulfans were highest in the upper sediment layer of the polynya lake (year 2014). In contrast, the highest DDT fluxes were found in 1980. These trends indicate that despite restrictions and regulations, bird transport continues to introduce considerable amounts of organohalogen pollutants to the Arctic regions with the exception of DDTs, which show successful decline, even when mediated by bird metabolism.

Rain Amplification of Persistent Organic Pollutants.

Scavenging of gas- and aerosol-phase organic pollutants by rain is an efficient wet deposition mechanism of organic pollutants. However, whereas snow has been identified as a key amplification mechanism of fugacities in cold environments, rain has received less attention in terms of amplification of organic pollutants. In this work, we provide new measurements of concentrations of perfluoroalkyl substances (PFAS), organophosphate esters (OPEs), and polycyclic aromatic hydrocarbons (PAHs) in rain from Antarctica, showing high scavenging ratios. Furthermore, a meta-analysis of previously published concentrations in air and rain was performed, with 46 works covering different climatic regions and a wide range of chemical classes, including PFAS, OPEs, PAHs, polychlorinated biphenyls and organochlorine compounds, polybromodiphenyl ethers, and dioxins. The rain–aerosol (KRP) and rain–gas (KRG) partition constants averaged 105.5 and 104.1, respectively, but showed large variability. The high field-derived values of KRG are consistent with adsorption onto the raindrops as a scavenging mechanism, in addition to gas–water absorption. The amplification of fugacities by rain deposition was up to 3 orders of magnitude for all chemical classes and was comparable to that due to snow. The amplification of concentrations and fugacities by rain underscores its relevance, explaining the occurrence of organic pollutants in environments across different climatic regions.

Brominated flame retardants extraction from waste electrical and electronic equipment-derived ABS using supercritical carbon dioxide.

Persistent organic pollutants such as brominated flame retardants represent a major problem in the end-of-life of polymer materials. This study investigates the extraction of brominated flame retardants (BFR) from real waste electrical and electronic equipment (WEEE) using supercritical carbon dioxide (sc-CO2). Sc-CO2 is a non-toxic solvent which possesses intermediate properties between liquids and gases which confer it high diffusivity and solubility. A batch of WEEE-derived acrylonitrile-butadienestyrene (ABS) was first characterized to determine its bromine and BFR composition which was found to be four times higher than the regulation limit set in 2019. Then, different parameters of the sc-CO2 process such as temperature, pressure, granulometry and the use of a co-solvent were studied to estimate the effect of each one on the BFR extraction efficiency. With the view to determine the recyclability of the treated polymer, the impact of the extraction process on the polymer material was also studied by Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC) and Size Exclusion Chromatography (SEC). The extraction process performed on <500µm particle size sample at 40°C and 500 bars during 6h and using ethanol as a co-solvent allowed to remove 43.5±0.9% of bromine, which was the maximum extraction rate obtained. Sc-CO2 extraction was found to be an efficient technique to remove tetrabromobisphenol A (TBBPA) but the tested conditions did not allow to remove enough polybromodiphenylethers (PBDE) to satisfy the regulation. Sc-CO2 process seems to be a promising pre-treatment method prior to mechanical recycling as no degradation effect on the polymer matrix was observed.

Integration of 103 Semivolatile Organic Compounds into One Multianalyte Method for Human Serum Analysis: An Innovative Approach within Exposure Assessment

Semivolatile organic compounds (SVOCs) are frequently detected in the environment, and humans are exposed to a mixture of chemicals via multiple exposure pathways. However, there are few data on health outcomes caused by the cumulative exposure or toxicological interactions, due to the absence of simultaneous analytical methods. Herein, we present a method for simultaneous determination of 103 SVOCs, including seven phthalate esters, seven polychlorinated biphenyls, 16 polycyclic aromatic hydrocarbons, five polybromodiphenyl ethers, and 68 pesticides, in 0.5 mL of serum. The two-step extraction coupled with gas chromatography-tandem mass spectrometry was described with a single chromatographic run within 36.65 min. Methodological parameters such as recovery rates, matrix effects, and limits of detection were studied and complied with the validation guidelines. The absolute and relative recoveries ranged from 65.45% to 123.83%, and the relative standard deviations were ≤21.43%. The detection limits were <0.41 μg L–1. This method was then successfully applied to the analysis of 99 real serum samples. The developed protocol achieved a limit of quantification at a level of parts per billion for all compounds and presented benefits for the control of confounding factors, cumulative exposure, and risk assessment in population studies.

Atmospheric deposition of semivolatile organic pollutants in European high mountains: Sources, settling and chemical degradation

Bulk atmospheric deposition samples, including wet and dry deposition, were collected during 2004–2006 in four high mountain European lakes: Skalnate Pleso (Tatra mountains, Slovakia), Gossenköllesee (Alps, Austria), Redon (Pyrenees, Spain), and Lochnagar (Grampian Mountains, Scotland). Samples were analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs), hexachlorobenzene (HCB), hexachlorocyclohexanes (HCHs), endosulfans, and polybromodiphenyl ethers (PBDEs).The deposition of PCBs, HCHs, and low brominated BDEs reflected baseline contributions from long range atmospheric transport. This was also the case for PAHs in Redon and Gossenköllesee, endosulfans in Lochnagar and Gossenköllesee and HCB in these three lakes. However, Skalnate received PAHs, endosulfans, and HCB from regional sources as it was the case for endosulfans in Redon. The distinct origin of these pollutants was reflected in the relative composition of some metabolites such as the proportion of endosulfan sulfate vs α- and β-endosulfans or the relative composition of BDE47 and BDE99.Wet deposition was the main process for atmospheric removal of PAHs, HCHs, and HCB. In addition, warm season revolatilization from soils and melting snow with subsequent condensation at low temperature were significant for volatile PAHs, HCB, low chlorinated PCBs, and endosulfans.Reaction with OH radicals was not a significant loss process of HCHs and HCB in remote areas, dominated by wet deposition, whereas PCBs and PAHs were significantly removed by both wet deposition and OH radical oxidation, the latter dominating in the highest altitude sites. Photolysis was the main atmospheric removal process of PBDEs, dominating over atmospheric deposition and OH depletion in all sites.

Optimization of a new selective pressurized liquid extraction methodology for determining organic pollutants in wild boar livers

In this study, a new selective pressurised liquid extraction (SPLE) methodology was optimised for determining about 70 organic pollutants (OPs) including organochlorine (OCPs), organophosphate (OPPs) and pyrethroid (PYRs) pesticides, polychlorinated biphenyls (PCBs), polybromodiphenyl ethers (PBDEs), as well as, polycyclic aromatic hydrocarbons (PAHs) in wild boar liver samples considering the temperature, pressure and time of contact between the solvent and the matrix as influential variables. Clean-up of extracts was performed by solid-phase extraction (SPE) using EZ-POP cartridges. Detection of OPs was carried out by gas chromatography (GC) coupled to tandem mass spectrometry (QqQ-MS/MS). This new approach offers:•A new non-time consuming SPLE methodology for determining about 70 OPs in wild boar.•Recoveries achieved ranged between 74 to 119 % with RSD less than 20 %.•Detection and quantification limits in the low to mid pg/g range.

Wild boar (Sus scrofa) as bioindicator for environmental exposure to organic pollutants

Organic pollutants (OPs) are widely distributed around the globe, their presence has become an issue of great concern in the last years due to their potential health effects. Wildlife biomonitoring of OPs has been nowadays a common approach to assess chemical exposure in wildlife and humans. In a sample of 60 wild boars (Sus scrofa) from NW Spain, we evaluated the suitability of using liver and hair samples for the assessment of exposure and bioaccumulation of polychlorinated biphenyls (PCBs) including dioxin and non-dioxin like PCBs (DLPCBs and NDLPCBs), organochlorine and organophosphate pesticides (OCPs and OPPs, respectively), polybromodiphenyl ethers (PBDEs), pyrethroids (PYRs) and polycyclic aromatic hydrocarbons (PAHs). Selective pressurized liquid extraction (SPLE) and liquid-liquid extraction (LLE) methodologies were used to determine the target OPs in liver and hair samples. Clean-up of extracts was performed by solid-phase extraction (SPE) using EZ-POP cartridges and detection by gas chromatography coupled to tandem mass spectrometry (GC-QqQ-MS/MS). We found a distribution pattern of ΣPAHs > ΣOCPs > ΣPYRs > ΣNDLPCBs > ΣOPPs > ΣDLPCBs > ΣPBDEs in liver and of ΣPAHs > ΣOCPs > ΣNDLPCBs > ΣPYRs > ΣOPPs > ΣDLPCBs > ΣPBDEs in hair. Significant correlations (p < 0.050) between the socio-demographic characteristics (gender, age and place) and OP concentrations of OCPs, PBDEs, PYRs, OPPs and PAHs were detected. Moderate correlation was found between HCB, PCB28, PCB157 and chlorpyrifos contents in both hair and liver samples. On the basis of these results, our data shows the correlation and complementary information given by both biological samples.

Legacy and Emerging Contaminants in Demersal Fish Species from Southern Norway and Implications for Food Safety.

The present study aimed at measuring the levels of legacy and emerging contaminants in fillet samples from four demersal fish caught in two fishing sites from Southern Norway, in order to assess possible implications for food safety. Levels of organochlorine compounds (OCs), organophosphate pesticides (OPs), polychlorinated biphenyls (PCBs), polybromodiphenyl ethers (PBDE), per- and polyfluoroalkyl substances (PFASs), and polycyclic aromatic hydrocarbons (PAHs) were measured in fillet from Atlantic cod (Gadus morhua), European plaice (Pleuronectes platessa), lemon sole (Microstomus kitt), and European flounder (Platichthys flesus) specimens. A negligible contamination by all the investigated chemicals was noted in both the fishing sites, as very low levels of OCs, PCBs, and PFASs were noted in a limited number of individuals for each species. Considering the levels of contaminants measured in fillets of the four demersal fish species, negligible risk for human health for Norwegian consumers can be supposed.

Occurrence of Halogenated and Organophosphate Flame Retardants in Sediments and Eels (Anguilla anguilla) From Bizerte Lagoon, Tunisia

Contamination by classic (polybromodiphenyl ethers, PBDEs) and emerging halogenated flame retardants (HFRs) like pentabromobenzene (PBEB), hexabromobenzene (HBB), decabromodiphenyl ethane (DBDPE ) and halogenated norbornenes (HNs), as well as organophosphate flame retardants (OPFRs) were investigated in sediment and eel (Anguilla Anguilla) samples from Bizerte Lagoon, northern Tunisia. This is the first time that OPFR levels have been reported in this area, showing higher concentrations than HFRs: from 9.77 to 164 ng/g dry weight (dw) and from 19.7 to 2154 ng/g lipid weight (lw) for sediment and eel samples, respectively. As regards HFRs, concentrations ranged from 3.30 to 28.5 ng/g dw in sediments and from 4.72 to 151 ng/g lw in eels. The relationship between OPFR and HFR concentrations in sediment and total organic content (TOC) was examined. Results suggested that OPFR levels were significantly correlated with TOC, whereas no correlation was found for HFRs and TOC. The study of potential health risks by eel consumption suggested that there is no significant human health risk associated with the dietary intakes for PBDEs.

Photodegradation of Decabromo Diphenyl Ether Flame Retardant in Poly (Acrylonitrile Butadiene Styrene) (ABS)

Decabromodiphenylether (DBDE) is a brominated flame retardant which belongs to the group of polybromodiphenylethers (PBDEs) often used as a fire resistant additive in various well known polymeric systems like polystyrene, poly(acrylonitrile-butadiene-styrene) (ABS), polypropylene, etc. This compound can be considered as a persistent organic pollutant and presents certain risks for the environment owing to the fact that it is bioaccumulable and not biodegradable. A detailed investigation, described here, was carried out on the effect of ultraviolet/visible radiation on DBDE in ABS with the aim to study the photolytic reactions of this molecule in the solid state, in order to improve the economic and ecological treatment of brominated plastic waste from waste electrical and electronic equipment (WEEE). This study presents new aspects of the photochemical degradation of DBDE/ABS systems in the solid state. The photodegradation of DBDE in ABS was followed by Fourier transform infrared spectroscopy (FTIR) as well as by thermogravimetrical analysis (TGA). Good agreement was obtained for the results of both analytical methods in terms of the overall photolysis of DBDE.

Incidence of persistent contaminants through blue mussels biomonitoring from Flekkefjord fjord and their relevance to food safety

ABSTRACTDredging activities can lead to the re-suspension of contaminated sediments, resulting in a potential hazard for the whole ecosystem and also for human health. Six-month active biomonitoring was performed in order to monitor the trends of different classes of both legacy (organochlorine – OCPs – and organophosphate (OPs) compounds and polychlorinated biphenyls – PCBs) and emerging (polybromodiphenyl ethers – PBDE – and per- and polyfluoroalkyl substances – PFASs) organohalogen compounds, as well as polycyclic aromatic hydrocarbons (PAHs), in blue mussel (Mytilus edulis spp.) specimens transplanted at different depths in the Flekkefjord fjord. Such biomonitoring was performed to evaluate the efficacy of sediment restoration activities and to check for the potential environmental risk for the biota and food safety for human seafood. Negligible contamination by OCPs, OPs, PBDEs and PFASs was noted in mussels over the 6-month biomonitoring, while a notable increase in the concentrations of PCBs and PAHs occurred in mussels transplanted at 15 m depth in three sampling sites within the fjord, as a consequence of an undersea landslide which occurred during restoration activities. Levels of PCBs and PAHs suggested a potential risk for mussel predators and also for the human health, as they exceeded the limit set by the European Commission for the consumption of bivalve molluscs. These results confirm the reliability of active biomonitoring to flank dredging activities aimed at ecosystem restoration in order to monitor the trend of contaminants and to estimate the potential risk for the aquatic communities and human health.

On-line coupling of thermal extraction with gas chromatography / tandem mass spectrometry for the analysis of semivolatile organic compounds in a few milligrams of indoor dust

An original multiresidue method based on thermal extraction (TE) and gas chromatography/tandem mass spectrometry (GC/MS/MS) was developed to simultaneously quantify, from a very small amount of sample (a few milligrams), a wide range of concerning SVOCs, including polycyclic musks, organochlorines (OCs), organophosphates (OPs), oxadiazolones, polycyclic aromatic hydrocarbons (PAHs), polybromodiphenylethers (PBDEs), polychlorobiphenyls (PCBs), phthalates and pyrethroids, in indoor settled dust. Method limits of quantification (LOQs) ranged from 5 ng g−1 for PCBs, oxadiazon, 4,4′-DDE and 4,4′-DDT to 2000 ng g−1 for DEHP for a 2 mg sample of sieved dust. The proposed method was successfully validated in terms of accuracy and precision via replicate analysis of four different standard reference materials (SRMs 1649b (Urban Dust), 2585 (Organic Contaminants in House Dust), 2786 and 2787 (Fine Atmospheric Particulate Matter)) supplied by the National Institute of Standards and Technology (NIST) and was applied to five real indoor settled dust samples collected in French schools. In addition, its performance was compared to that of a previously published method based on pressurized liquid extraction (PLE) and GC/MS/MS. The different results obtained demonstrate the advantages of the proposed method over conventional methods and illustrate its two main features: i) its ease of use and very rapid implementation in only three steps (sieving, weighing and analysis), which make it particularly appropriate for environmental monitoring programs and large-scale studies, and ii) its ability to precisely and accurately quantify a wide range of SVOCs from trace (a few ng g−1) to highly concentrated (several mg g−1) compounds from only 2 mg of sieved dust.