Long-term relationships among pesticide applications, mobility, and soil erosion in a vineyard watershed.

Agricultural pesticide use has increased worldwide during the last several decades, but the long-term fate, storage, and transfer dynamics of pesticides in a changing environment are poorly understood. Many pesticides have been progressively banned, but in numerous cases, these molecules are stable and may persist in soils, sediments, and ice. Many studies have addressed the question of their possible remobilization as a result of global change. In this article, we present a retro-observation approach based on lake sediment records to monitor micropollutants and to evaluate the long-term succession and diffuse transfer of herbicides, fungicides, and insecticide treatments in a vineyard catchment in France. The sediment allows for a reliable reconstruction of past pesticide use through time, validated by the historical introduction, use, and banning of these organic and inorganic pesticides in local vineyards. Our results also revealed how changes in these practices affect storage conditions and, consequently, the pesticides' transfer dynamics. For example, the use of postemergence herbicides (glyphosate), which induce an increase in soil erosion, led to a release of a banned remnant pesticide (dichlorodiphenyltrichloroethane, DDT), which had been previously stored in vineyard soil, back into the environment. Management strategies of ecotoxicological risk would be well served by recognition of the diversity of compounds stored in various environmental sinks, such as agriculture soil, and their capability to become sources when environmental conditions change.

Particle-Dissolved Phase Partition of Polychlorinated Biphenyls in High Altitude Alpine Lakes.

We investigated whether polychlorinated biphenyls (PCBs) partitioning between the dissolved and particulate phases in two high altitude alpine lakes was determined by the quantity, size structure, or composition of suspended particles. Within- and between-lakes differences in water-particulate phase partition coefficient (Kp) were not related to total suspended matter, phytoplankton biomass, or taxonomic composition. Yet, a seasonal relationship between Kp and Kow was detected for both lakes, revealing equilibrium of PCBs partition when lakes were ice covered. On the contrary, PCBs partitioning between particles and water appeared kinetically limited during the open water season. Partition is therefore mainly governed by thermodynamic laws during the ice-covered period, while none of the tested physical or biological parameters seemed to explain the distribution of these particle-reactive contaminants in the open water period. PCBs were always mainly associated with particulate matter, but partitioning within different particulate size-fractions varied between seasons and between years during open water periods. When ice cover is absent, PCBs were mainly adsorbed on microplankton, the largest phytoplanktonic size fraction, which is the least likely to get grazed by pelagic microconsumers.

Historical profiles of PCB in dated sediment cores suggest recent lake contamination through the "halo effect".

We investigated the major sources of polychlorinated biphenyls (PCB) and interpreted the environmental fate processes of these persistent organic pollutants in the past and current PCB contamination of three large, urbanized, French peri-alpine lakes. Dated sediment cores were analyzed in order to reconstruct and compare the historical contamination in all three lakes. Stratigraphic changes of PCB contents and fluxes were considered as revealing the temporal dynamics of PCB deposition to the lakes and the distribution of the seven indicator congeners (further referred to as PCBi) as an indicator of the main contamination origin and pathway. Although located within a single PCB industrial production region, concentration profiles for the three lakes differed in timing, peak concentration magnitudes, and in the PCBi congeners compositions. PCBi fluxes to the sediment and the magnitude of the temporal changes were generally much lower in Lake Annecy (0.05-2 ng·cm(-2)·yr(-1)) as compared to Lakes Geneva (0.05-5 ng·cm(-2)·yr(-1)) and Bourget (5-290 ng·cm(-2)·yr(-1)). For all three lakes, the paramount contamination occurred in the early 1970s. In Lakes Annecy and Bourget, PCB fluxes have declined and plateaued at 0.5 and 8 ng·cm(-2)·yr(-1), respectively, since the early 1990s. In Lake Geneva, PCB fluxes have further decreased by the end of the XX(th) century and are now very low. For the most contaminated lake (Lake Bourget), the high PCBi flux (5-290 ng·cm(-2)·yr(-1)) and the predominance of heavy congeners for most of the time period are consistent with a huge local input to the lake. This still high rate of Lake Bourget is explained by transport of suspended solids from one of its affluents, polluted by an industrial point source. Intermediate historical levels and PCBi distribution over time for Lake Geneva suggest a mixed contamination (urban point sources and distant atmospheric transport), while atmospheric deposition to Lake Annecy explains its lowest contamination rate. The presently low contamination levels recorded in Lake Geneva correspond to atmospheric inputs, but the recent PCBi distribution of Lake Annecy, enriched in relatively heavy congeners, reveals a contamination by the neighboring Lake Bourget, following a halo effect of about 40 km radius.

Impact of land-use on PAH transfer in sub-surface water as recorded by CaCO3 concretions in urban underground structures (Paris, France).

In densely populated urban areas, the pressure on water resources is considerable and will tend to intensify over the next decades. Preserving water resources therefore seems fundamental, but many questions remain as to the transfer of contaminants to subsurface waters in these largely sealed areas. Because of their toxicity and persistence in the environment, this work focused on the study of polycyclic aromatic hydrocarbons (PAHs), ubiquitous pollutants mainly produced by human activities. To better understand the main factors leading to the retention or transport of these pollutants in urban environments, vertical transects, from the surface to several meters down, were established on three study sites in or near Paris (France), selected according to an urbanization gradient. Soil samples collected at the surface and urban secondary carbonate deposits (USCD), similar to cave speleothems, sampled underground in quarries and aqueducts were analyzed. As the hydrophobic properties of PAHs favor their sorption onto organic matter, the latter was also studied using organic carbon analysis and UV fluorescence spectroscopy. The USCD located closest to the urbanized surface contained high concentrations of PAHs (76.8 ± 5.3 ng g-1), while the USCD located at greater depth with organic soil on the surface contained the lowest amount of PAHs (2.9 ± 0.4 ng g-1), and no PAHs with log KOC > 5. The results highlight the predominant role played by the presence of organic topsoil at the surface in retaining and storing large amounts of PAHs (1914-2595 ng. gsoil-1), particularly the most hydrophobic ones (i.e. 60% of the 15 PAHs are characterized by a Log KOC >5), which are also the most toxic. The lithology and thickness of the bedrock (between the surface and the USCD) also play an important role in the retention of PAHs, particularly those adsorbed on the particulate phase.

Polycyclic aromatic hydrocarbon record in an urban secondary carbonate deposit over the last three centuries (Paris, France).

Preserving water resources and limiting pollution are central environmental issues in the current context of intense anthropization. Among organic pollutants, polycyclic aromatic hydrocarbons (PAHs) are commonly analysed as part of water quality assessments. After being emitted into the atmosphere, these persistent organic pollutants are deposited on the continental surface, where they are transported to the aquatic environment by run-off and infiltration waters. Mainly due to anthropogenic emissions, PAHs can therefore be considered as a proxy for human activities. Urban secondary carbonate deposits (USCDs), similar to cave speleothems, have recently been studied for their potential as natural archives of water quality. However, USCDs have never been used to trace water organic pollution and only a few studies on PAHs in speleothems are available. This study focuses on a well-dated USCD covering the last 300 years from the Great Aqueduct of Belleville (north-east of Paris, France). The aim is to determine the nature and variation of trapped organic compounds over time and to discuss their origin, transport, and link with changes in soil occupation due to human activities. To do so, high-resolution solid-phase UV fluorescence imaging analyses were combined with chemical analyses of PAHs and organic carbon carried out on low-weight samples. The results show that PAHs have been present in urban surface water for 300 years. Over the last few decades, a 7-fold increase is observed, accompanied by a change in the pollution source, enriched in high-molecular-weight PAHs, probably linked to urban dust. This study also reveals modes of transport directly influenced by changes in the soil occupation that are very different from those usually encountered in natural environments. This work thus paves the way for a better long-term understanding of the impact of human activity on the transfer of pollutants to sub-surface waters.

The biological invasion of an apex predator (Silurus glanis) amplifies PCB transfer in a large lake food web.

Invasive species can affect food web structure possibly modifying the transfer of pollutants in ecosystems but this facet of biological invasion remains largely unexplored. We examined how trophic and ontogenetic characteristics of the invasive European catfish could differ from its native counterpart, the Northern pike, possibly resulting in the amplification of PCB transfer to the higher trophic levels in a large lake food web. The PCB contents of catfish and pike were on average low (Æ©7 PCBi 42.4 ± 38.6 ng g-1 ww and 37.9 ± 49.4 ng g-1 ww respectively) and dominated by PCB153 (~35 % of the PCB contamination). Only the largest pike (126 cm) slightly exceeded the European sanitary threshold of 125 ng g-1 ww Æ©6 PCBi-NDL. Both species increased in trophic position with body size while catfish had clearly higher littoral reliance than pike indicating they exploited complementary trophic niches. PCB biomagnification was identified only for catfish (PCB153, Æ©7 PCBi) leading to trophic magnification factor of ~5. PCB ontogenetic bioaccumulation was pervasive for catfish (PCB101, PCB118, PCB153, PCB138 and Æ©7 PCBi) and identified for pike only regarding PCB101. The derived size accumulation factors (~1.02) indicated a size-doubling PCB contamination of ~40 cm for catfish. This finding suggested that catfish would exceed the European sanitary threshold at body size larger than 168 cm possibly constraining their commercial exploitation. Our results highlighted that the invasive catfish was a littoral-oriented apex predator occupying an alternative trophic niche as compared to pike thereby modifying the lake food web structure that resulted in an enhancement of PCB transfer to higher trophic levels. The biomagnification and ontogenetic bioaccumulation of catfish underlined the impact of this biological invasion on the fate of PCB in the ecosystem. Finally, the remarkable inter-individual PCB contamination suggested variable inter-individual PCB exposure likely associated to localized hotspots of PCB contamination in the lake.

Evolution of pace-of-life syndrome under conditions of maternal PCB contamination and global warming in early life stages of cold stenothermic fish (Arctic char).

The end of the 20th century was characterised by rapid modifications of ecosystem functioning under different pressures (such as eutrophication and toxic pollution). Increasing temperatures in the context of global warming could have indirect consequences, such as increased bioavailability of hydrophobic organic pollutants amongst aquatic species. According to the "pace-of-life syndrome" (POLS) theory, these stressors could lead to covariations in many life traits. Lake Bourget is the largest natural lake in France and has been highly polluted from the fifties to the eighties both with a high load of nutrients (wastewater discharge) and polychlorinated biphenyls (PCBs) (industrial effluent discharge). Despite improvements in water quality since the 21st century, PCB levels are still higher than the United States Environmental Protection Agency cut-off for wildlife protection. The population of Arctic char, a cold stenothermic salmonid, has remained low in Lake Bourget for the last ten years despite restocking efforts and complete re-oligotrophication. We hypothesised that PCB pollution can affect the Arctic char population and that the increase in water temperature could magnify the effects of PCB. Thus, this study aimed to investigate the effects of maternal PCB contamination on offspring using a multiparametric and multiscale approach. Female Arctic char were contaminated with PCB before spawning, and each fertilised spawn was incubated at two temperatures (4 and 8.5 °C). The results showed that co-exposure to increased temperature and maternal PCB contamination influenced biodemographic, physiological, and behavioural parameters. The effects were highly dependant on the developmental stage. Based on the POLS theory, a continuum of life traits that may reflect potential physiological and behavioural modifications in response to these concurrent stressors is highlighted.

Polycyclic aromatic hydrocarbon dynamics in soils along proglacial chronosequences in the Alps.

Polycyclic aromatic hydrocarbons (PAHs) were studied in the soils of three proglacial areas in France (Noir and Chardon Glaciers) and Italy (Miage Glacier). PAH contents, PAH stocks and PAH contents normalized to the total organic carbon contents (PAHs/TOC ratio) were investigated along proglacial soil chronosequences to infer their evolutions with soil age (from 3 to 4200 years), where the PAH contamination was only related to long-range atmospheric transport. Evolutions of PAH and TOC contents, PAHs/TOC ratio and PAH stock were fitted with exponential and logarithmic relations. For the three proglacial areas, PAH contents increased rapidly during the first 150 years of soil development, ranged from 4 to 152 ng·g-1, and showed a strong relationship with total organic carbon (TOC) contents (r = 0.83, p < 0.05). The joint increase of PAH and TOC contents suggested that PAH accumulation in soils were not only driven by PAH inputs but also by the capacity of soils to store these contaminants. PAH contents in the oldest soils (from 1200 BCE and 2200 BCE) were similar than for soils from 1850 CE. The period 1850-2019 CE corresponded to a decrease in the PAHs/TOC ratio suggesting both a faster accumulation of TOC than PAHs and a dilution effect of PAHs already present in soils. For the oldest soils, the PAHs/TOC ratio appeared similar to those for soils from 1850 CE, with values ranging from 0.48 to 2.06 ng·mg-1, suggesting an equilibrium between both parameters for soils older than 170 years. Finally, PAH stocks ranged from 0.41 mg·m-2 to 6.80 mg·m-2 in the youngest and oldest soils, respectively. These results do not allow us to identify the same period of greatest emission as other studies (estimated ~1960), but they revealed changes in the capacity of soils to store these pollutants.

Microplastic pollution of worldwide lakes.

Studies on microplastic (MP) pollution in lakes are recent, although the problem of MP particles in the oceans was first discovered in the 1970s. The first study on lakes was published in 2011. Since then, to our knowledge, 98 lakes have been investigated worldwide. In recent years, studies on this topic have increased worldwide, particularly those focusing on urbanised lakes. Most of the plastic waste in the seas and oceans originates from the terrestrial environment and inland waters. Moreover, lakes are potential temporary or long-term MP accumulators, according to the residence time of water. They are also of high interest for biodiversity, ecology, and the economy. Lacustrine ecosystems may suffer the same fate as marine ecosystems, or even worse, owing to their greater exposure. With the significant focus on ocean and sea contamination, contamination of freshwater ecosystems and lakes is a new and rising topic. However, as a new field of research, several methodological issues have been raised. The team diversity worldwide has led to contrasting sampling techniques and materials, sample treatments, analyses, and presentation of results. Consequently, it is necessary to determine several consensuses between scientific teams in order to work together with accuracy, produce comparable results, speed up knowledge sharing and reduce the reproducibility crisis. This review focuses on (1) MP contamination in 98 worldwide lakes. We identify (2) the theoretical sources of MPs and provide (3) an estimate of MP pollution in different compartments of the lakes based on current state-of-the-art methods. In addition, we also report (4) the predominant MP size classes and polymer types. Finally, we suggest (5) several recommendations to build a consensus between all the working teams to facilitate decision-making by public authorities.

Water-level fluctuation enhances sediment and trace metal mobility in lake littoral.

Water-level fluctuation (WLF) is a widespread management action in lakes and reservoirs whose impacts on contaminant fate have seldom been investigated. We used near shore hourly measurements (n = 2122) of turbidity (contaminant proxy) and water velocity (sediment resuspension proxy) to track high-frequency contaminant dynamics during a 0.6 m change in water level observed in autumn 2017 in a large French lake. Simultaneously, discrete trace metal measurements highlighted that trapped sediment was more contaminated and finer than surficial sediment supporting that suspended particles (measured by turbidity) were a preferential medium for contaminant mobility. General additive models involving tensor products revealed the enhancement of wind-speed and river discharge effects on turbidity with water draw down. The decrease of the explained deviances by the models over time-lags indicated short time-scale response of turbidity to external forcing. Three of the four major turbid events occurred at the lowest water-level and were concomitant of sediment resuspension as well as precipitation events and/or river flood suggesting a complex interplay among in-lake and watershed processes at controlling sediment mobility during the WLF. These results shed in light that WLF can affect lake littoral hydrodynamic cascading up to the enhancement of contaminant mobility. Sediment resuspension may be an overlooked feature of WLF increasing contamination risk and exposure for littoral organisms with widespread ecological consequences due to the large number of water-level regulated ecosystems.

Diversity, Functions and Antibiotic Resistance of Sediment Microbial Communities From Lake Geneva Are Driven by the Spatial Distribution of Anthropogenic Contamination.

Lake sediments are natural receptors for a wide range of anthropogenic contaminants including organic matter and toxicants such as trace metals, polycyclic aromatic hydrocarbons, polychlorinated biphenyls that accumulate over time. This contamination can impact benthic communities, including microorganisms which play a crucial role in biogeochemical cycling and food-webs. The present survey aimed at exploring whether anthropogenic contamination, at a large lake scale, can influence the diversity, structure and functions of microbial communities associated to surface sediment, as well as their genetic potential for resistance to metals and antibiotics. Changes in the characteristics of these communities were assessed in surface sediments collected in Lake Geneva from eight sampling sites in October 2017 and May 2018. These sampling sites were characterized by a large concentration range of metal and organic compound contamination. Variation between the two sampling periods were very limited for all sampling sites and measured microbial parameters. In contrast, spatial variations were observed, with two sites being distinct from each other, and from the other six sites. Benthic communities from the most contaminated sampling site (Vidy Bay, near the city of Lausanne) were characterized by the lowest bacterial and archaeal diversity, a distinct community composition, the highest abundance of antibiotic resistance genes and functional (respiration, denitrification, methanogenesis, phosphatase, and beta-glucosidase) activity levels. The second sampling site which is highly influenced by inputs from the Rhône River, exhibited low levels of diversity, a distinct community composition, high abundance of antibiotic resistance genes and the highest bacterial abundance. Overall, our results suggest that local anthropogenic contamination, including organic matter and toxicants, is a major driver of the diversity and functioning of sediment-microbial communities in Lake Geneva. This highlights the need to consider benthic microbial communities and a suite of complementary ecotoxicological endpoints for more effective environmental risk assessments of contaminants in lake sediments.

Tracking sources and transfer of contamination according to pollutants variety at the sediment-biota interface using a clam as bioindicator in peri-alpine lakes.

Point pollution sources may differently impact lakes littoral, possibly leading to local ecological risks. The concomitant chemical analysis of littoral-benthic organisms and sediment can provide insights into the bioavailability and thus the ecological risk of contaminants. In this study, the autochthonous Corbicula fluminea was used to assess the sources and transfer of six trace metals (TMs) and fourteen Polycyclic Aromatic Hydrocarbons (PAHs) to the littoral-benthic biota of a large lake. The contaminant concentrations spatially varied with a value scale from 1 to 280 000 times along the lake littoral in both the sediment and clams. Multiple linear regressions were performed to explain the spatial variability of Corbicula fluminea contamination by considering both watershed and in-lake sources. The concentration of the sum of PAHs in clams was significantly correlated with sediment contamination, suggesting that PAHs contamination of the benthic biota mainly occur from the sediment. Most of the internal TM concentrations of clams were significantly correlated with stormwater drainage areas in the lake watershed, highlighting the importance of stormwater runoffs in the littoral biota contamination. The transfer of TMs and PAHs was assessed through the bioconcentration factor defined as the ratio of internal and sediment concentrations. As, Cd, Cu, Zn and light molecular weight PAHs were more bioconcentrated in C. fluminea than Pb, Sn and heavy molecular weight PAHs, suggesting differences in their bioavailability. This study underlines the relevance of using autochthonous organisms as bioindicators of lake littoral biota contamination concomitantly with sediment matrices, and illustrates the challenge of tracking pollution sources in lakes.

Adsorption kinetics of 4-chlorophenol onto granular activated carbon in the presence of high frequency ultrasound.

This work describes the results of investigations carried out to examine the adsorption kinetics of 4-chlorophenol (4-CP) from aqueous solution containing tert-butyl alcohol (10%, v/v) onto granular activated carbon (GAC) in the presence of ultrasound of different high frequencies (516, 800 and 1660 kHz) and acoustic powers (15.2, 21.5, 31.1 and 38.3 W). The main objective of this study is to describe the mechanism of ultrasound-assisted adsorption rather than the enhancement of adsorption capacity. Sonochemical degradation of 4-CP was studied in the absence and presence of tert-butyl alcohol. The sonolysis of 4-CP is effectively inhibited by the addition of tert-butyl alcohol (10%, v/v) and very little 4-CP degradation occurs, indicating that little or no pyrolysis of the compound occurs. Without addition of tert-butyl alcohol, after 300 min and at 1660 kHz, the removal of 4-CP in the presence of ultrasound for an acoustic power of 38.3 W was nearly total (99%), but in the conventional method only 60% was eliminated. In this case, the removal of 4-CP by GAC in the ultrasound-assisted technique is due to both adsorption and ultrasonic degradation, but the removal by simple stirring is only due to adsorption, which makes a direct comparison unacceptable. In order to distinguish sonochemical degradation and adsorption of 4-CP onto GAC and to make an exact and practical comparison of the adsorption in the absence and presence of ultrasound, kinetic adsorption experiments were conducted using aqueous solution containing 10% (v/v) tert-butyl alcohol. The obtained results show that both adsorption rate and adsorbed amount were significantly enhanced and improved in the presence of ultrasound for all the studied frequencies and powers. The enhancement of adsorption is favored by increasing ultrasonic power. Adsorption kinetic data were modeled using the liquid-film mass transfer equation and intraparticle diffusion model. The values of the intraparticle diffusion coefficient obtained in the presence of ultrasound are greater than that obtained in the absence of ultrasound. In the initial period of adsorption, where external mass transfer is assumed to predominate, liquid-film mass transfer coefficients significantly increased by the assistance of ultrasound. These results indicate that ultrasound enhances the mass transport in the pores as well as across the boundary layer. This effect increased with increasing ultrasonic power for the three studied frequencies. The average order for the studied ultrasonic waves according to the initial adsorption rate, the intraparticle diffusion coefficient and the liquid-film mass transfer coefficient is 516 kHz>800 kHz>1660 kHz.

PCB mass budget in a perialpine lake undergoing natural decontamination in a context of global change.

Despite the fact that PCB contamination of the global environment has been extensively studied in the last decades, the fate of these compounds in freshwater ecosystems is not fully understood and an important knowledge gap remains regarding the understanding of PCB dynamics and fate in perialpine lakes. This study relied on both field sampling performed and modeling to accurately identify the main fluxes involved in the PCB dynamics into the French perialpine Lake Bourget from 2013 to 2017. Our results show that the main inputs responsible for the PCB loading of the water column are tributaries inflows (~90%) rather than atmospheric inputs which could be related to the high catchment area over lake surface area ratio (i.e., 13). The main mechanism responsible for the lake natural decontamination was sediment burial (76%) due to the effect of the biological pump coupled with a high sedimentation rate. Volatilization represented 19% of the loss of PCBs from the water column and was mainly controlled by the high PCB concentration in water. These mechanisms are susceptible to be affected by the impact of the global change (increase of temperature, modification of the primary production rate) in the near future.

Sonochemical and photosonochemical degradation of 4-chlorophenol in aqueous media.

The degradation of 4-chlorophenol (4-CP) in aqueous media by 516 kHz ultrasonic irradiation was investigated in order to clarify the degradation mechanism. The degradation of concentrated 4-CP solution by means of ultrasound, UV irradiation and their combined application was also studied. The obtained results indicate that *OH radical are the primary reactive species responsible for 4-CP ultrasonic degradation. Very little 4-CP degradation occurs if the sonolysis is carried out in the presence of the *OH radical scavenger tert-butyl alcohol, also indicating that little or no pyrolysis of the compound occurs. The dominant degradation mechanism is the reaction of substrate with *OH radicals at the gas bubble-liquid interface rather than high temperature direct pyrolysis in ultrasonic cavities. This mechanism can explain the lower degradation rate of the ionic form of 4-CP that is partly due to the rapid dissociation of *OH radicals in alkaline solutions. The sonochemical destruction of concentrated 4-CP aqueous solution is obtained with low rate. Coupling photolysis with ultrasound irradiation results in increased efficiency compared to the individual processes operating at common conditions. Interestingly, the photosonochemical decomposition rate constant is greater than the additive rate constants of the two processes. This may be the result of three different oxidative processes direct photochemical action, high frequency sonochemistry and reaction with ozone produced by UV irradiation of air, dissolved in liquid phase because of the geyser effect of ultrasound streaming. Additionally, the photodecomposition, at 254 nm, of hydrogen peroxide produced by ultrasound generating *OH radical can partly explain the destruction enhancement.

Ultrasound-assisted removal of malachite green from aqueous solution by dead pine needles.

The dead needles of Aleppo pine (Pinus halepensis) were tested as a possible sorbent for the removal of malachite green from aqueous solutions in the absence and presence of ultrasound. Batch process was employed for sorption kinetic and equilibrium studies. Sorption experiments indicated that the sorption capacity was dependent of operating variables. Both the rate and the amount of malachite green sorption are markedly increased in the presence of the ultrasonic field. The dye removal with the assistance of ultrasound was enhanced with the increase of sorbate initial concentration and temperature, and with the decrease of sorbent dosage and ionic strength. The combination of stirring and ultrasound leads to an improvement of the removal of dye. The sorption kinetics was controlled by the intraparticle diffusion. The intraparticle diffusion coefficient increased 1.7 times in the presence of ultrasound and up to 3.6 times in the combined process. The sorption capacity, estimated according to the Freundlich model, indicates that ultrasound enhanced the sorption properties of the sorbent. The effect of ultrasound on the improvement of dye sorption is due to a variety of physical and mechanical effects as well as to thermal properties. The combination of ultrasound and stirring for the sorption process was shown to be of interest for the treatment of wastewaters contaminated with malachite green.

Looking at biological community level to improve ecotoxicological assessment of freshwater sediments: report on a first French-Swiss workshop.

The first French-Swiss workshop on ecotoxicology of freshwater sediment communities was co-organized by the French Research Institute of Science and Technology for Environment and Agriculture (Irstea) and the Swiss Centre for Applied Ecotoxicology (Ecotox Centre EAWAG-EPFL) in Villié-Morgon (Beaujolais Region, France) on April 27-28, 2017. The workshop brought together scientists working in different fields of expertise (ecotoxicologists, ecologists, environmental chemists…), environmental stakeholder groups and managers, as well as economic players (start-ups and consultancies) to better connect research needs of potential end-users with research outputs. The objectives of this workshop were (i) to establish the state of the art of research in the characterization of sediment contamination and in the evaluation of the effects on sediment-associated biological communities and ecosystem functioning and (ii) to give an overview of the French and Swiss regulations dealing with the assessment of contaminated sediments in freshwater ecosystems. The ultimate goal was to collectively identify research needs and knowledge gaps, as well as to highlight ways to improve the ecotoxicological assessment of sediments in freshwater environments by further considering the structure and functions of associated microbial and invertebrate communities.

Modeling of adsorption isotherms of phenol and chlorophenols onto granular activated carbon. Part II. Models with more than two parameters.

The adsorption equilibrium isotherms of five phenolic compounds, phenol, 2-chlorophenol, 4-chlorophenol, 2,4-dichlorophenol, and 2,4,6-trichlorophenol, from aqueous solutions onto granular activated carbon were studied and modeled. In order to determine the best-fit isotherm, the experimental equilibrium data were analyzed using thirteen adsorption isotherm models with more than two-parameter; nine three-parameter equations - the Redlich-Peterson, Sips, Langmuir-Freundlich, Fritz-Schlunder, Radke-Prasnitz (three models), Tóth, and Jossens isotherms - three four-parameter equation - the Weber-van Vliet, Fritz-Schlunder, and Baudu isotherms - and one five-parameter equation - the Fritz-Schlunder isotherm. The results reveal that the adsorption isotherm models fitted the experimental data in the order: Baudu (four-parameter)>Langmuir-Freundlich (three-parameter)>Sips (three-parameter)>Fritz-Schlunder (five-parameter)>Tóth (three-parameter)>Fritz-Schlunder (four-parameter)>Redlich-Peterson (three-parameter). The influence of solution pH on the adsorption isotherms of 4-CP was investigated. It was shown that the solution pH has not an effect on the adsorption isotherms for pH

Modeling of adsorption isotherms of phenol and chlorophenols onto granular activated carbon. Part I. Two-parameter models and equations allowing determination of thermodynamic parameters.

The adsorption equilibrium isotherms of five phenolic compounds from aqueous solutions onto granular activated carbon (GAC) were studied and modeled. Phenol (Ph), 2-chlorophenol (2-CP), 4-chlorophenol (4-CP), 2,4-dichlorophenol (DCP), and 2,4,6-trichlorophenol (TCP) were chosen for the adsorption tests. To predict the adsorption isotherms and to determine the characteristic parameters for process design, seven isotherm models: Langmuir (five linear forms), Freundlich, Elovich, Temkin, Fowler-Guggenheim, Kiselev, and Hill-de Boer models were applied to experimental data. The results reveal that the adsorption isotherm models fitted the data in the order: Fowler-Guggenheim>Hill-de Boer>Temkin>Freundlich>Kiselev>Langmuir isotherms. Adsorption isotherms modeling shows that the interaction of phenolic compounds with activated carbon surface is localized monolayer adsorption, that is adsorbed molecules are adsorbed at definite, localized sites. Each site can accommodate only one molecule. The interaction among adsorbed molecules is repulsive and there is no association between them, adsorption is carried out on energetically different sites and is an exothermic process. Uptake of phenols increases in the order Ph<2-CP<4-CP

Avoid the PCB mistakes: A more sustainable future for ionic liquids.

Based on our original knowledge and experience on both polychlorinated biphenyls (PCBs) identification in aquatic ecosystems, and use of ionic liquids (ILs) as solvents and/or co-catalysts in green chemistry, we drawn a dared comparison between these two families. Indeed, PCBs has been used during several decades for their new properties, but are now considered as prevalent and persistent pollutants; some toxic effects on environment or human are still revealed. ILs, often designated as "green solvents" are increasingly used in numerous applications, but few studies reported about their environmental impact are still controversial. Through a parallel between properties and applications of PCBs and ILs, we wondered if history could not repeat itself, and how to provide a better future for ILs. Here, we provide some interesting comparisons and we discuss which tracks it could be important to follow for ILs applications in order to avoid the errors done with PCBs.