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.

[Departement_IRSTEA]Eaux [TR1_IRSTEA]ARCEAU | The purpose of this work is to assess the effectiveness of two grass covers (buffer zone and grass-covered inter-row), to reduce pesticide leaching, and subsequently to preserve groundwater quality. Lower amounts of pesticides leached through grass-cover soil columns (2.7e24.3% of the initial amount) than the bare soil columns (8.0e55.1%), in correspondence with their sorption coefficients. Diuron was recovered in higher amounts in leachates (8.9e32.2%) than tebuconazole (2.7e12.9%), in agreement with their sorption coefficients. However, despite having a sorption coefficient similar to that of diuron, more procymidone was recovered in the leachates (10.2e55.1%), probably due to its facilitated transport by dissolved organic matter. Thus even in this very permeable soil, higher organic matter contents associated with grass-cover reduce the amount of pesticide leaching and limit the risk of groundwater contamination by the pesticides. The results of diuron and tebuconazole transfer through undisturbed buffer zone soil columns are in agreement with field observations on the buffer zone.

[Departement_IRSTEA]Eaux [TR1_IRSTEA]BELCA | Little information is available on the environmental occurrence and ecotoxicological effects of pharmaceutical gestagens released in the aquatic environment. Since eighteen different gestagens were found to be used in France, preliminary exposure and hazard assessment were done. Predicted environmental concentrations (PECs) suggest that if parent gestagens are expected to be found in the ng l−1 range, some active metabolites could be present at higher concentrations, although limited data on metabolism and environmental fate limit the relevance of PECs. The biological effects are not expected to be restricted to progestagenic activity. Both anti-androgenic activity (mainly for cyproterone acetate, chlormadinone acetate and their metabolites) and estrogenic activity (mainly for reduced metabolites of levonorgestrel and norethisterone) should also occur. All these molecules are likely to have a cumulative effect among themselves or with other xenoestrogens. Studies on occurrence, toxicity and degradation time are therefore needed for several of these compounds.

[Departement_IRSTEA]MA [TR1_IRSTEA]QSA / HYDRECO | International audience | The concentrations of dissolved and particulate polycyclic aromatic hydrocarbons (PAHs) were monitored in waters of the Rhône River (France) every fortnight for a full calendar year, from June 1994 to May 1995. All flood events occurring over the course of the experiment were sampled at higher frequency to better quantify the impact of these extreme hydrological episodes on the annual export of PAHs to the Mediterranean Sea. This time-series indicates that more than 90% of the annual load of particulate PAHs is transported during flood episodes, with 77% discharged during the course of only one extreme flood event occurring in November 1994. During these intense events, riverine particles are depleted in PAHs while at low river discharge particles are PAH-enriched. Dissolved PAHs were less variable and less abundant than adsorbed PAHs, consistently with the low solubility of these compounds.

Concerns about the use of residues from municipal solid waste incinerators (MSWI) in construction materials usually focus on the potential for heavy metals and organic chemicals to leach into drainage waters under the influence of rain.We hypothesised that high level of salts in the MSWI leachates may cause more of a problem, particularly on soil physico-chemical properties. Both bottom ash (BA) and Solidified Air Pollution Control residue (SAPCr) leachates were added to experimental grassland plots. The amounts of Na+ increased by up to 13% in soils supplemented with each leachate. A decrease of the soil total porosity (−14%) was evidence of a subsequent adverse physical effect of this strong salinity. The potential for the grass cover type (species composition or density) to limit this adverse effect was discussed. Laboratory tests allowed us to determine that undiluted SAPCr induced slaking of aggregates accompanied by a strong decrease of aggregate stability, to 49% of control values. Undiluted BA induced dispersion of clays and others fine particles, which are then dislodged and transported into pores, causing blockage and decreasing total porosity. Clay dispersion followed by aggregate collapse occurred when soil solution contaminated by SAPCr was diluted by rainwater. This work stressed the importance of accounting for mineral contaminants, such as salts, when conducting an assessment of waste reuse scenarios.

16 ref.;Nø special | National audience

National audience

This article describes a stochastic method to calculate the annual pollutant loads and its application over several years at the outlet of three catchments drained by separate storm sewers. A stochastic methodology using Monte Carlo simulations is proposed for assessing annual pollutant load, as well as the associated uncertainties, from a few event sampling campaigns and/or continuous turbidity measurements (representative of the total suspended solids concentration (TSS)). Indeed, in the latter case, the proposed method takes into account the correlation between pollutants and TSS. The developed method was applied to data acquired within the French research project BINOGEV^ (innovations for a sustainable management of urban water) at the outlet of three urban catchments drained by separate storm sewers. Ten or so event sampling campaigns for a large range of pollutants (46 pollutants and 2 conventional water quality parameters: TSS and total organic carbon (TOC)) are combined with hundreds of rainfall events for which, at least one among three continuously monitored parameters (rainfall intensity, flow rate, and turbidity) is available. Results obtained for the three catchments show that the annual pollutant loads can be estimated with uncertainties ranging from 10 to 60%, and the added value of turbidity monitoring for lowering the uncertainty is demonstrated. A low inter-annual and inter-site variability of pollutant loads, for many of studied pollutants, is observed with respect to the estimated uncertainties, and can be explained mainly by annual precipitation.

Nitrogen (N) is an input essential to agriculture which produces plant but also animal proteins. N cycle is a biological complex cycle, with biological fixation converting atmospheric unreactive di-nitrogen into many reactive nitrogen forms (Nr), essential for life. Nr forms are implicated in many transformations in air, water and soil, as well as within living organisms, until recovering to the N2 form through denitrification. These natural processes were amplified by the development of industrial husbandry and the massive use of N industrial fertilizers, making N expensive for forffarmers. Furthermore, its management in agriculture and its low efficiency in plant production and even more in animal production lead to losses to the environment. The most mediatized one is nitrate lixiviation with its impacts on water quality. N losses to atmosphere have become a matter of concern for the French public authorities since about twenty years, for their impacts on greenhouse balance (nitrous oxide N2 0), air quality and ecosystems and biodiversity (ammonia NH3 , and nitrogen oxides NOx). The costs of abatement strategies are more or less amortized thanks to the profits realized in economy (N expenses in agriculture) and for society (human health, global changes…). | L’azote (N) est un intrant indispensable à une agriculture productrice de protéines végétales mais surtout animales. Le cycle de l’azote est un cycle biogéochimique complexe, dont l’essentiel des entrées dans la biosphère est constitué par la fixation biologique. Toutes les formes d’azote chimiquement et biologiquement actives constituent l’azote dit réactif. Il l’eau et le sol, ainsi qu’au sein des êtres vivants, allant jusqu’au retour à sa forme diazote par la dénitrification. Ces processus naturels ont été amplifiés par le développement de l’élevage industriel et le recoursmassif aux engrais industriels azotés. Or l’azote coûte cher financièrement aux agriculteurs, et sa gestion en agriculture génère des rejets vers l’environnement liés aux faibles rendements d’utilisation de l’azote par les végétaux et surtout par les animaux. Les rejets les plus médiatisés sont les nitrates, avec les impacts sur la qualité des eaux. Les pertes vers l’atmosphèrepréoccupent les pouvoirs publics français depuis une vingtaine d’années, du fait de leurs impacts sur le réchauffement global de l’atmosphère (protoxyde d’azote, N2 0) mais aussi sur la qualité de l’air (ammoniac NH3 , et oxydes d’azote NOX). Les parades pour réduire les émissions de ces polluants et gaz à effet de serre ont également un coût, plus ou moins amorti selon lescomposés émis et/ou les postes émetteurs concernés grâce aux bénéfices économiques (poste azote en agriculture) et sociaux (santé humaine, changements globaux…) réalisés.