The freshwater lakes of southwestern France are subject to the development of invasive macrophytes which are associated with mercury (Hg) contamination of the food web. The aim of this study was to determine the bioavailability of methylmercury (MeHg) produced by plant roots in aquatic ecosystems. A microcosm experiment was performed using isotopically enriched inorganic Hg at environmental concentrations (1 µg ¹⁹⁹IHg·L⁻¹). For all conditions, total Hg in fish as well as Hg species associated with different compartments (water, sediments, plant roots, fish) were analyzed by gas chromatography-inductively coupled plasma-mass spectrometry (GC-ICP-MS). In addition, sediment, plants, and fish gut microbiota were studied by MiSEQ sequencing. Some strains were isolated and tested for their ability to methylate Hg. The results revealed ¹⁹⁹MeHg production in plant roots and the presence of this form in fish (tissues and gut), highlighting a MeHg trophic transfer. Moreover, methylator bacteria were identified from the gut contents of the fish when they were in the presence of plants. Some of them were related to bacteria found in the plant roots. On the basis of these results, the transfer of MeHg and bacteria from plants to fish is highlighted; in addition, Hg methylation is strongly suspected in the fish gut, potentially increasing the Hg bioaccumulation.

Bioremediation of produced waters has been widely investigated in the last decades. More recently, microalgae-based treatments have been developed to produce biomass. The objective of this study was to determine, at lab scale, the remediation efficiency of three origin of microorganisms: a consortium of three halotolerant and halophilic microalgae and their associated bacteria, bacteria from liquid digestate, and aromatic-degrading bacteria selected to perform bioaugmentation. The medium was composed of artificial oil-produced water and seawater, and contained nutrients from liquid digestate. In order to identify what plays a role in nitrogen, chemical oxygen demand, and aromatics compounds elimination, and to determine the effectiveness of bioaugmentation to treat this mix of waters, 16S rRNA analyses were performed. Combination of microorganisms from different origins with the selected aromatic-degrading bacteria were also realized, to determine the effectiveness of bioaugmentation to treat these waters. Each population of microorganisms achieved similar percentage of removal during the biological treatment, with 43–76%, 59–77%, and 86–93% of elimination for ammonium, chemical oxygen demand, and aromatic compounds (with 50% of volatilization), respectively, after 7 days, and up to with 100%, 77%, and 99% after 23 days, demonstrating that in the case of this produced water, bioaugmentation with the specialized aromatic-degrading bacteria had no significant impact on the treatment. Regarding in detail the populations present and active during the tests, those from genus Marinobacter always appeared among the most active microorganisms, with some strains of this genus being known to degrade aromatic compounds.

Industrial residues with high concentrations of hexavalent chromium [Cr(VI)], characterized by an alkaline pH (between 9 and 13) and high salinity (around 100 psu), were used as a source for extremophilic chromium-resistant and -reducing microorganisms. An investigation of biodiversity through MiSeq showed the presence of 20 bacterial classes, with Bacilli (47%), Negativicutes (15%), Bacteriodia (8%), Gammaproteobacteria (7%) and Clostridia (5%) being the most abundant. The bioprospection allowed the cultivation of 87 heterotrophic bacterial colonies and 17 bacterial isolates at the end of the isolation, and screening procedures were obtained. The isolates were related to Cellulosimicrobium aquatile, C. funkei, Acinetobacter radioresistens, Staphylococcus equorum, S. epidermis, Brachybacterium paraconglometratum, Glutamicibacter creatinolyticus, Pseudomonas songnenensis, Microbacterium algeriense and Pantoea eucalypti, most of them being resistant to Cr(VI). Resistances of up to 400 ${\mathrm{m}\mathrm{g}.\mathrm{L}}^{-1}$ of chromate were obtained for four related strains (QReMLB55A, QRePRA55, QReMLB33A and QReMLB44C). The C. aquatile strain QReMLB55A and the P. songnenensis strain QReMLB33A were exposed to ${\mathrm{K}}_2{\mathrm{C}\mathrm{r}}_2{\mathrm{O}}_7$ (200 ${\mathrm{m}\mathrm{g}.\mathrm{L}}^{-1}$) under optimal conditions, diminishing 94% and 24% of the Cr(VI) in 6 days, respectively. These strains exhibited a high potential for chromium remediation biotechnologies.

In search of a Cr(VI) removal bioprocess, within a circular economy perspective, we combined two autochthonous bacterial consortia obtained from industrial residues and an agricultural waste (rice husk of Oryza sativa). After characterizing the rice husk (rh) properties, the bacterial growth and biofilm formation, we studied the taxonomical profile of the bacterial consortia (C55, C33, and C21, the last is a combination 2:1 of the previous ones). By using SEM analysis, we confirmed the presence of a smooth layer of exopolysaccharides (EPS) over the rice husk surface. Total bacterial biodiversity, assessed through MiSeq analysis, showed that the addition of Cr(VI) stimulated the growth of two main populations ( Cellulosimicrobium and Siminovitchia ) while inhibiting Peptoniphilus , Cutibacterium and Rhodococcus . We also evaluated chromium depletion, in batch experiments, with particular emphasis on its sorption to the agroresidue and its biotransformation by the biomass. When exposed to 200 mg.L ^-1 Cr(VI), the system containing both rh and the bacterial consortium completely removed Cr(VI) from the effluent with half-times between 53 and 67 h. The combination of Cr(VI) biosorption by rh and its biotransformation to Cr(III) by bacterial consortia confirmed an effective synergy capable of removing 92% of Cr(VI). This work supports the potential of an innovative bioprocess based on bacterial biofilms grown on rh for the mitigation of Cr(VI) contamination.