Under laboratory conditions, the effects of thiamethoxam were investigated in larvae, pupae and emerging honey bees after exposure at larval stages with different concentrations in the food (0.00001 ng/µL, 0.001 ng/µL and 1.44 ng/µL). Thiamethoxam reduced the survival of larvae and pupae and consequently decreased the percentage of emerging honey bees. Thiamethoxam induced important physiological disturbances. It increased acetylcholinesterase (AChE) activity at all developmental stages and increased glutathione-S-transferase (GST) and carboxylesterase para (CaEp) activities at the pupal stages. For midgut alkaline phosphatase (ALP), no activity was detected in pupae stages, and no effect was observed in larvae and emerging bees. We assume that the effects of thiamethoxam on the survival, emergence and physiology of honey bees may affect the development of the colony. These results showed that attention should be paid to the exposure to pesticides during the developmental stages ofthe honey bee. This study represents the first investigation of the effects of thiamethoxam on the development of A. mellifera following larval exposure.

International audience | Seabirds integrate bioaccumulative contaminants via food intake and have revealed geographical trends of contamination in a variety of ecosystems. Pre-fledging seabird chicks are particularly interesting as bioindicators of chemical contamination, because concentrations in their tissues reflect primarily dietary sources from the local environment. Here we measured 14 trace elements and 18 persistent organic pollutants (POPs) in blood of chicks of skuas that breed in four sites encompassing a large latitudinal range within the southern Indian Ocean, from Antarctica (Adélie Land, south polar skua Catharacta maccormicki), through subantarctic areas (Crozet and Kerguelen Islands, brown skua C. lonnbergi), to the subtropics (Amsterdam Island, C. lonnbergi). Stables isotopes of carbon (δ13C, feeding habitat) and nitrogen (δ15N, trophic position) were also measured to control for the influence of feeding habits on contaminant burdens. Concentrations of mercury (Hg) and selenium (Se) were very high at all the four sites, with Amsterdam birds having the highest concentrations ever reported in chicks worldwide (4.0 ± 0.8 and 646 ± 123 µg g-1 dry weight, respectively). Blood Hg concentrations showed a clear latitudinal pattern, increasing from chicks in Antarctica to chicks in the subantarctic and subtropical islands. Interestingly, blood Se concentrations showed similar between-population differences to Hg, suggesting its involvement in protective mechanisms against Hg toxicity. Chicks’ POPs pattern was largely dominated by organochlorine pesticides, in particular DDT metabolites and hexachlorobenzene (HCB). Skua chicks from subantarctic islands presented high concentrations and diversity of POPs. By contrast, chicks from the Antarctic site overall had the lowest concentrations and diversity of both metallic and organic contaminants, with the exception of HCB and arsenic. Skua populations from these sites, being naturally exposed to different quantities of contaminants, are potentially good models for testing toxic effects in developing chicks in the wild.

International audience | Aquatic ecosystems of the Bolivian Altiplano (∼3800 m a.s.l.) are characterized by extreme hydro-climatic constrains (e.g., high UV-radiations and low oxygen) and are under the pressure of increasing anthropogenic activities, unregulated mining, agricultural and urban development. We report here a complete inventory of mercury (Hg) levels and speciation in the water column, atmosphere, sediment and key sentinel organisms (i.e., plankton, fish and birds) of two endorheic Lakes of the same watershed differing with respect to their size, eutrophication and contamination levels. Total Hg (THg) and monomethylmercury (MMHg) concentrations in filtered water and sediment of Lake Titicaca are in the lowest range of reported levels in other large lakes worldwide. Downstream, Hg levels are 3-10 times higher in the shallow eutrophic Lake Uru-Uru than in Lake Titicaca due to high Hg inputs from the surrounding mining region. High percentages of MMHg were found in the filtered and unfiltered water rising up from <1 to ∼50% THg from the oligo/hetero-trophic Lake Titicaca to the eutrophic Lake Uru-Uru. Such high %MMHg is explained by a high in situ MMHg production in relation to the sulfate rich substrate, the low oxygen levels of the water column, and the stabilization of MMHg due to abundant ligands present in these alkaline waters. Differences in MMHg concentrations in water and sediments compartments between Lake Titicaca and Uru-Uru were found to mirror the offset in MMHg levels that also exist in their respective food webs. This suggests that in situ MMHg baseline production is likely the main factor controlling MMHg levels in fish species consumed by the local population. Finally, the increase of anthropogenic pressure in Lake Titicaca may probably enhance eutrophication processes which favor MMHg production and thus accumulation in water and biota.

Mediterranean Basin ecosystems, their unique biodiversity, and the key services they provide are currently at risk due to air pollution and climate change, yet only a limited number of isolated and geographically-restricted studies have addressed this topic, often with contrasting results. Particularities of air pollution in this region include high O3 levels due to high air temperatures and solar radiation, the stability of air masses, and dominance of dry over wet nitrogen deposition. Moreover, the unique abiotic and biotic factors (e.g., climate, vegetation type, relevance of Saharan dust inputs) modulating the response of Mediterranean ecosystems at various spatiotemporal scales make it difficult to understand, and thus predict, the consequences of human activities that cause air pollution in the Mediterranean Basin

International audience | Abstract Nanomaterials are increasingly being used to improve the properties and functions of common building materials. A new type of self-cleaning cement incorporating TiO2 nanomaterials (TiO2-NMs) with photocatalytic properties is now marketed. This promising cement might provide air pollution-reducing properties but its environmental impact must be validated. During cement use and aging, an altered surface layer is formed that exhibits increased porosity. The surface layer thickness alteration and porosity increase with the cement degradation rate. The hardened cement paste leaching behavior has been fully documented, but the fate of incorporated TiO2-NMs and their state during/after potential release is currently unknown. In this study, photocatalytic cement pastes with increasing initial porosity were leached at a lab-scale to produce a range of degradation rates concerning the altered layer porosity and thickness. No dissolved Ti was released during leaching, only particulate TiO2-NM release was detected. The extent of release from this batch test simulating accelerated worst-case scenario was limited and ranged from 18.7 ± 2.1 to 33.5 ± 5.1 mg of Ti/m2 of cement after 168 h of leaching. TiO2-NMs released into neutral aquatic media (simulate pH of surface water) were not associated or coated by cement minerals. The TiO2-NM release mechanism is suspected to start from freeing of TiO2-NMs in the altered layer pore network due to partial cement paste dissolution followed by diffusion into the bulk pore solution to the surface. The extent of TiO2-NM release was not solely related to the cement degradation rate.

[Departement_IRSTEA]Eaux [TR1_IRSTEA]BELCA | International audience | This study evaluates the combined effects of two contaminants (copper and a herbicide S-metolachlor) and temperature on the early life stages of the Pacific oyster Crasssotrea gigas,which is native to Arcachon Bay (southwest France). The responses of D-larvae, obtained fromwild and cultivated oysters,were investigated for one year during the oyster breeding period at different sampling sites and compared with the response of D-larvae from a commercial hatchery. Embryotoxicity was measured by considering the percentage of abnormal D-shaped larvae. Normal development of embryos occurred only from 22 °C to 26 °C. There were synergistic effects of copper at low and high temperatures. Native oysters appear particularly sensitive to an increase in water temperature, suggesting a future increase in the percentage of larval abnormalities as a result of global climate change. Hatchery oysters represent a good alternative model for studying the effects of both pollutants and climate change stressors.

Polycyclic aromatic hydrocarbons (PAHs) are hardly biodegradable carcinogenic organic compounds. Bioremediation is a commonly used method for treating PAH contaminated environments such as soils, sediment, water bodies and wastewater. However, bioremediation has various drawbacks including the low abundance, diversity and activity of indigenous hydrocarbon degrading bacteria, their slow growth rates and especially a limited bioavailability of PAHs in the aqueous phase. Addition of nutrients, electron acceptors or co-substrates to enhance indigenous microbial activity is costly and added chemicals often diffuse away from the target compound, thus pointing out an impasse for the bioremediation of PAHs. A promising solution is the adoption of bioelectrochemical systems. They guarantee a permanent electron supply and withdrawal for microorganisms, thereby circumventing the traditional shortcomings of bioremediation. These systems combine biological treatment with electrochemical oxidation/reduction by supplying an anode and a cathode that serve as an electron exchange facility for the biocatalyst. Here, recent achievements in polycyclic aromatic hydrocarbon removal using bioelectrochemical systems have been reviewed. This also concerns PAH precursors: total petroleum hydrocarbons and diesel. Removal performances of PAH biodegradation in bioelectrochemical systems are discussed, focussing on configurational parameters such as anode and cathode designs as well as environmental parameters like porosity, salinity, adsorption and conductivity of soil and sediment that affect PAH biodegradation in BESs. The still scarcely available information on microbiological aspects of bioelectrochemical PAH removal is summarised here. This comprehensive review offers a better understanding of the parameters that affect the removal of PAHs within bioelectrochemical systems. In addition, future experimental setups are proposed in order to study syntrophic relationships between PAH degraders and exoelectrogens. This synopsis can help as guide for researchers in their choices for future experimental designs aiming at increasing the power densities and PAH biodegradation rates using microbial bioelectrochemistry.

International audience | Gentle remediation options (GRO) are based on the combined use of plants, associated microorganisms and soil amendments, which can potentially restore soil functions and quality. We studied the effects of three GRO (aided-phytostabilisation, in situ stabilisation and phytoexclusion, and aided-phytoextraction) on the soil microbial biomass and respiration, the activities of hydrolase enzymes involved in the biogeochemical cycles of C, N, P, and S, and bacterial community structure of trace element contaminated soils (TECS) from six field trials across Europe. Community structure was studied using denaturing gradient gel electrophoresis (DGGE) fingerprinting of Bacteria, α- and β-Proteobacteria, Actinobacteria and Streptomycetaceae, and sequencing of DGGE bands characteristic of specific treatments. The number of copies of genes involved in ammonia oxidation and denitrification were determined by qPCR. Phytomanagement increased soil microbial biomass at three sites and respiration at the Biogeco site (France). Enzyme activities were consistently higher in treated soils compared to untreated soils at the Biogeco site. At this site, microbial biomass increased from 696 to 2352 mg ATP kg-1 soil, respiration increased from 7.4 to 40.1 mg C-CO2 kg-1 soil d-1, and enzyme activities were 2-11-fold higher in treated soils compared to untreated soil. Phytomanagement induced shifts in the bacterial community structure at both, the total community and functional group levels, and generally increased the number of copies of genes involved in the N cycle (nirK, nirS, nosZ, and amoA). The influence of the main soil physico-chemical properties and trace element availability were assessed and eventual site-specific effects elucidated. Overall, our results demonstrate that phytomanagement of TECS influences soil biological activity in the long term.

Filterable PM2.5 concentrations and their chemical characterizations were analyzed for 67 boilers and 25 indirect furnaces located in the Metropolitan Area of Costa Rica from February 2014 to November 2015. The PM2.5 samples were characterized by their composition, focusing on trace elements, inorganic ions and organic and elemental carbon. The results of PM2.5 concentrations ranged from 72 to 735 mgm-3, with the highest concentrations found for sources using biomass fuel, particularly Type B boilers, and the lowest values for diesel boilers. Further speciation of fine particulate matter (PM) showed significant levels of vanadium and nickel for boilers that use heavy fuel oil (bunker); 4886 and 1942 μgm-3, respectively. Copper and manganese were the most relevant metals for biomass burning sources, due to plant absorption from the soil. As for ion concentration, sulfate presented the highest concentrations for biomass boilers and furnaces, whereas chloride only presented the highest concentrations for furnaces. To complete the balance, organic and elemental carbon (OC and EC) analyses were made, in which biomass burning sources presented values five times higher than oil fuels. A Spearman's correlation analysis was made for the data set, revealing significant relationships between heavy metals, sulfate, and fine PM with respect to heavy fuel oil. For the biomass sources, the correlations pointed to K, Na, Mn and, in some cases, oxygen. | Se analizaron las concentraciones filtrables de PM2.5 y sus caracterizaciones químicas para 67 calderas y 25 hornos indirectos ubicados en el Área Metropolitana de Costa Rica desde febrero de 2014 hasta noviembre de 2015. Las muestras de PM2.5 se caracterizaron por su composición, centrándose en oligoelementos, iones inorgánicos y carbono orgánico y elemental. Los resultados de las concentraciones de PM2.5 variaron de 72 a 735 mgm-3, con las concentraciones más altas encontradas para fuentes que utilizan combustible de biomasa, particularmente calderas Tipo B, y el valores más bajos para calderas diesel. Una mayor especiación de partículas finas (PM) mostró una significativa niveles de vanadio y níquel para calderas que utilizan fuel oil pesado (bunker); 4886 y 1942 mgm-3, respectivamente. El cobre y el manganeso fueron los metales más relevantes para las fuentes de combustión de biomasa, debido a Absorción de plantas del suelo. En cuanto a la concentración de iones, el sulfato presentó las mayores concentraciones para calderas y hornos de biomasa, mientras que el cloruro solo presentó las concentraciones más altas para los hornos. Para completar el balance, se realizaron análisis de carbono orgánico y elemental (OC y EC), en los cuales las fuentes de combustión de biomasa presentaron valores cinco veces superiores a los combustibles derivados del petróleo. La correlación de Spearman. Se realizó un análisis para el conjunto de datos, revelando relaciones significativas entre metales pesados, sulfato y PM fino con respecto al fuelóleo pesado. Para las fuentes de biomasa, las correlaciones apuntaron a K, Na, Mn y, en algunos casos, oxígeno. | As concentrações filtráveis ​​de PM2,5 e suas caracterizações químicas foram analisadas para 67 caldeiras e 25 fornos indiretos localizados na Região Metropolitana da Costa Rica de fevereiro de 2014 a novembro de 2015. As amostras de PM2,5 foram caracterizadas por sua composição, com foco em oligoelementos, íons inorgânicos e carbono orgânico e elementar. Os resultados para as concentrações de PM2,5 variaram de 72 a 735 mgm-3, com as concentrações mais altas encontradas para fontes que usam combustível de biomassa, particularmente caldeiras Tipo B, e os valores mais baixos para caldeiras a diesel. A maior especiação de partículas finas (PM) mostrou níveis significativos de vanádio e níquel para caldeiras que usam óleo combustível pesado (bunker); 4886 e 1942 mgm-3, respectivamente. O cobre e o manganês foram os metais mais relevantes para as fontes de combustão da biomassa, devido à absorção das plantas do solo. Em relação à concentração de íons, o sulfato apresentou as maiores concentrações para caldeiras e fornos a biomassa, enquanto o cloreto apresentou as maiores concentrações apenas para os fornos. Para completar o balanço, foram realizadas análises de carbono orgânico e elementar (OC e EC), nas quais as fontes de combustão de biomassa apresentaram valores cinco vezes maiores que os combustíveis derivados do petróleo. A correlação de Spearman. Uma análise foi realizada para o conjunto de dados, revelando relações significativas entre metais pesados, sulfato e MP fino em relação ao óleo combustível pesado. Para fontes de biomassa, as correlações apontaram para K, Na, Mn e, em alguns casos, oxigênio. | Universidad Nacional, Costa Rica | Universidad Autónoma Metropolitana, México | Escuela de Ciencias Ambientales

A number of methods have been reported for determining hydrophobic organic compound adsorption to dispersed carbon nanotubes (CNTs), but their accuracy and reliability remain uncertain. We have evaluated three methods to investigate the adsorption of phenanthrene (a model polycyclic aromatic hydrocarbon; PAH) to CNTs with different physicochemical properties; dialysis tube (DT) protected negligible depletion solid phase microextraction (DT-nd-SPME), ultracentrifugation and filtration using various types of filters. Dispersed CNTs adhered to the unprotected PDMS-coated fibers used in nd-SPME. Protection of the fibers from CNT adherence was investigated with hydrophilic DT, but high PAH sorption to the DT was observed. The efficiency of ultracentrifugation and filtration to separate CNTs from the water phase depended on CNT physicochemical properties. While non-functionalized CNTs were efficiently separated from the water phase using ultracentrifugation, incomplete separation of carboxyl functionalized CNTs was observed. Filtration efficiency varied with different filter types (composition and pore size), and non-functionalized CNTs were more easily separated from the water phase than functionalized CNTs. Sorption of phenanthrene was high (<70%) for three of the filters tested, making them unsuitable for the assessment of phenanthrene adsorption to CNTs. Filtration using a hydrophilic polytetrafluoroethylene (PTFE) filter membrane (0.1 µm) was found to be a simple and precise technique for the determination of phenanthrene adsorption to a range of CNTs, efficiently separating all types of CNTs and exhibiting a good and highly reproducible recovery of phenanthrene (82%) over the concentration range tested (70-735 µg/L). | acceptedVersion