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 | This study examined the long-term effects of the landfill disposal of untreated urban waste for soil fertilization on the prevalence and antibiotic resistance profiles of various human opportunistic pathogens in soils from Burkina Faso. Samples were collected at three sites in the periphery of Ouagadougou during two campaigns in 2008 and 2011. At each site, amendment led to changes in physico-chemical characteristics as shown by the increase in pH, CEC, total C, total N, and metal contents. Similarly, the numbers of total heterotrophic bacteria were higher in the amended fields than in the control ones. No sanitation indicators, i.e., coliforms, Staphylococci, and Enterococci, were detected. Pseudomonas aeruginosa and Burkholderia cepacia complex (Bcc) were d e t e c t e d a t a l o w l e v e l i n o n e a m e n d e d f i e l d. Stenotrophomonas maltophilia was detected from both campaigns at the three sites in the amended fields and only once in an unamended field. Diversity analysis showed some oppor-tunistic pathogen isolates to be closely related to reference clinical strains responsible for nosocomial-or community-acquired infections in Northern countries. Antibiotic resistance tests showed that P. aeruginosa and Bcc isolates had a wild-type phenotype and that most S. maltophilia isolates had a multi-drug resistance profile with resistance to 7 to 15 antibiotics. Then we were able to show that amendment led to an increase of some human opportunistic pathogens including multi-drug resistant isolates. Although the application of untreated urban waste increases both soil organic matter content and therefore soil fertility, the consequences of this practice on human health should be considered.

International audience

International audience

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

Polycyclic aromatic hydrocarbons (PAHs) concentrations in PM10 and PM2.5 particles were measured at 14 monitoring sites (12 for PM10 and 2 for PM2.5), located in the Metropolitan Area of Costa Rica, from January to November 2013. High-volume air samplers with pretreated quartz filters were used to collect the particles. The analytical determination was carried out using high-performance liquid chromatography (HPLC). The most abundant PAHs were benzo[a]anthracene, indeno(1,2,3-cd)pyrene, dibenz[a,h]anthracene and acenaphthylene. Ratios obtained by correlating the concentration of some PAHs, both PM10 and PM2.5, suggest that gasoline and diesel vehicles are the main sources in the area being studied. This is consistent with the results obtained when applying the positive matrix factorization (PMF) analysis, since vehicles accounted for 62–74% of total emissions in the area; burning wood fuel was the second source of emissions, contributing between 7 and 15%; and road dust was third, with almost 8%. | Se midieron las concentraciones de hidrocarburos aromáticos policíclicos (HAP) en partículas PM10 y PM2.5 en 14 sitios de monitoreo (12 para PM10 y 2 para PM2.5), ubicados en el Área Metropolitana de Costa Rica, de enero a noviembre de 2013. Alto volumen Se utilizaron muestreadores de aire con filtros de cuarzo pretratados para recoger las partículas. La determinación analítica se realizó mediante cromatografía líquida de alta resolución (HPLC). Los HAP más abundantes fueron benzo [a] antraceno, indeno (1,2,3-cd) pireno, dibenz [a, h] antraceno y acenaftileno. Los ratios obtenidos al correlacionar la concentración de algunos HAP, tanto de PM10 como de PM2,5, sugieren que los vehículos de gasolina y diésel son las principales fuentes en el área de estudio. Esto es consistente con los resultados obtenidos al aplicar el análisis de factorización matricial positiva (PMF), ya que los vehículos representaron 62-74% de las emisiones totales en el área; la quema de leña fue la segunda fuente de emisiones, contribuyendo entre el 7 y el 15%; y el polvo de la carretera ocupó el tercer lugar, con casi el 8%. | Universidad Nacional, Costa Rica | Laboratorio de Análisis Ambiental. Facultad de Ciencias Ambientales. Universidad Nacional, Costa Rica