Co-contamination of ligand-like antibiotics (e.g., tetracyclines and quinolones) and heavy metals prevails in the environment, and thus the complexation between them is involved in environmental risks of antibiotics. To understand toxicological significance of the complex, effects of metal coordination on antibiotics' toxicity were investigated. The complexation of two antibiotics, oxytetracycline and ciprofloxacin, with three heavy metals, copper, zinc, and cadmium, was verified by spectroscopic techniques. The antibiotics bound metals via multiple coordination sites and rendered a mixture of various complexation speciations. Toxicity analysis indicated that metal coordination did modify the toxicity of the antibiotics and that antibiotic, metal, and their complex acted primarily as concentration addition. Comparison of EC₅₀ values revealed that the complex commonly was highest toxic and predominately correlated in toxicity to the mixture. Finally, environmental scenario analysis demonstrated that ignoring complexation would improperly classify environmental risks of the antibiotics.

Spatially explicit estimates of critical loads of nitrogen (N) deposition (CLNdₑₚ) for nutrient enrichment in aquatic ecosystems were developed for the Rocky Mountains, USA, using a geostatistical approach. The lowest CLNdₑₚ estimates (<1.5 ± 1 kg N ha⁻¹ yr⁻¹) occurred in high-elevation basins with steep slopes, sparse vegetation, and abundance of exposed bedrock and talus. These areas often correspond with areas of high N deposition (>3 kg N ha⁻¹ yr⁻¹), resulting in CLNdₑₚ exceedances ≥1.5 ± 1 kg N ha⁻¹ yr⁻¹. CLNdₑₚ and CLNdₑₚ exceedances exhibit substantial spatial variability related to basin characteristics and are highly sensitive to the NO₃ ⁻ threshold at which ecological effects are thought to occur. Based on an NO₃ ⁻ threshold of 0.5 μmol L⁻¹, N deposition exceeds CLNdₑₚ in 21 ± 8% of the study area; thus, broad areas of the Rocky Mountains may be impacted by excess N deposition, with greatest impacts at high elevations.

Salinization is a major and growing threat to freshwater ecosystems, yet its effects on aquatic invertebrates have been poorly described at a community-level. Here we use a controlled experimental setting to evaluate short-term stream community responses to salinization, under conditions designed to replicate the duration (72 h) and intensity (up to 5 mS cm⁻¹) of salinity pulses common to Mediterranean rivers subjected to mining pollution during runoff events. There was a significant overall effect, but differences between individual treatments and the control were only significant for the highest salinity treatment. The community response to salinization was characterized by a decline in total invertebrate density, taxon richness and diversity, an increase in invertebrate drift and loss of the most sensitive taxa. The findings indicate that short-term salinity increases have a significant impact on the stream invertebrate community, but concentrations of 5 mS cm⁻¹ are needed to produce a significant ecological response.

International audience | Fish farming in barrage pond is a rearing system commonly used worldwide. Obtaining good water quality is essential to improve sustainability of these ecosystems, both for health of fish consumers and environmental considerations. However, ponds are often located in agricultural landscape, but few study reports impact of pesticide pressure on these ecosystems. This study characterizes five sites in Northeastern France. This work establishes an initial framework for pesticide monitoring with the aim to improve understanding of the fate of pesticides in ponds. This framework is based on surveys indicating managements and Geographical Information System (GIS) for five ponds and their watersheds (sites: C-0, C-25, C-45, C-75 and C-85) and completes with some analysis of a large spectrum of pesticide residues in surface waters. Watersheds show a gradient of crop proportion ranging from 0% to 82% of the watershed area, mainly rapeseed, wheat, barley and maize. Ponds were representative of local Northeastern France management. Many pesticides, and also nutrients, were measured in water with concentrations varying between sites and seasons. The sum of quantified molecules ranged from 0.17 mu g/l for site C-0 (March) to 8.81 mu g/l for site C-25 (October). Concentrations of metaldehyde, quinmerac, isoproturon and bentazon were sometimes above 1 mu g/l. There is a strong connection between pond and watershed, due to water supply throughout the fish production cycle. Sites with small pond/big watershed are the most exposed to acute contamination a few days after spraying because water discharges are not diluted.

International audience | Alkylphenols and alkylphenol ethoxylates (APE) are toxics classified as endocrine-disrupting compounds; they are used in detergents, paints, herbicides, pesticides, emulsifiers, wetting and dispersing agents, antistatic agents, demulsifiers, and solubilizers. Many studies have reported the occurrence of alkylphenols in different environmental matrices, though none of these studies have yet to establish a comprehensive overview of such compounds in the water cycle within an urban environment. This review summarizes APE concentrations for all environmental media throughout the water cycle, from the atmosphere to receiving waters. Once the occurrence of compounds has been assessed for each environmental compartment (urban wastewater, wastewater treatment plants [WWTP], atmosphere, and the natural environment), data are examined in order to understand the fate of APE in the environment and establish their geographical and historical trends. From this database, it is clear that the environment in Europe is much more contaminated by APE compared to North America and developing countries, although these APE levels have been decreasing in the last decade. APE concentrations in the WWTP effluent of developed countries have decreased by a factor of 100 over the past 30 years. This study is aimed at identifying both the correlations existing between environmental compartments and the processes that influence the fate and transport of these contaminants in the environment. In industrial countries, the concentrations observed in waterways now represent the background level of contamination, which provides evidence of a past diffuse pollution in these countries, whereas sediment analyses conducted in developing countries show an increase in APE content over the last several years. Finally, similar trends have been observed in samples drawn from Europe and North America.

International audience | * Introduction : Acidic and metal(oid)-rich topsoils resulted after 34 years of continuous operations of a copper smelter in the Puchuncaví valley, central Chile. Currently, large-scale remediation actions for simultaneous in situ immobilization of metals and As are needed to reduce environmental risks of polluted soils. Aided phytostabilization is a cost-effective alternative, but adequate local available soil amendments have to be identified and management options have to be defined. * Materials and methods : Efficacy of seashell grit (SG), biosolids (B), natural zeolite (Z), and iron-activated zeolite (AZ), either alone or in mixtures, was evaluated for reducing metal (Cu and Zn) and As solubilization in polluted soils under laboratory conditions. Perennial ryegrass was used to test phytotoxicity of experimental substrates. * Results : Soil neutralization to a pH of 6.5 with SG, with or without incorporation of AZ, significantly reduces metal (Cu and Zn) solubilization without affecting As solubilization in soil pore water; furthermore, it eliminates phytotoxicity and excessive metal(oid) accumulation in aerial plant tissues. Addition of B or Z to SG-amended soil does not further reduce metal solubilization into soil pore water, but increase As solubilization due to excessive soil neutralization (pH > 6.5); however, no significant As increase occurs in aerial plant tissues. * Conclusion : Simultaneous in situ immobilization of metal(oid) in acidic topsoils is possible through aided phytostabilization.

We present a new formulation of the acidification model MAGIC that uses decomposer dynamics to link nitrogen (N) cycling to carbon (C) turnover in soils. The new model is evaluated by application to 15–30 years of water chemistry data at three coniferous-forested sites in the Czech Republic where deposition of sulphur (S) and N have decreased by >80% and 40%, respectively. Sulphate concentrations in waters have declined commensurately with S deposition, but nitrate concentrations have shown much larger decreases relative to N deposition. This behaviour is inconsistent with most conceptual models of N saturation, and with earlier versions of MAGIC which assume N retention to be a first-order function of N deposition and/or controlled by the soil C/N ratio. In comparison with earlier versions, the new formulation more correctly simulates observed short-term changes in nitrate leaching, as well as long-term retention of N in soils. The model suggests that, despite recent deposition reductions and recovery, progressive N saturation will lead to increased future nitrate leaching, ecosystem eutrophication and re-acidification.

Evidence from a multi-date regional-scale analysis of both high-flow and annual-average water quality data from Galloway, south-west Scotland, demonstrates that forest land cover continues to exacerbate freshwater acidification. This is in spite of significant reductions in airborne pollutants. The relationship between freshwater sulphate and forest cover has decreased from 1996 to 2006 indicating a decrease in pollutant scavenging. The relationship between forest cover and freshwater acidity (pH) is, however, still present over the same period, and does not show conclusive signs of having declined. Furthermore, evidence for forest cover contributing to a chlorine bias in marine ion capture suggests that forest scavenging of sea-salts may mean that the forest acidification effect may continue in the absence of anthropogenic pollutant inputs, particularly in coastal areas.

For a given emissions inventory, the general levels of air pollutants and the spatial distribution of their concentrations are determined by the physiochemical state of the atmosphere. Apart from the trivial seasonal and daily cycles, most of the variability is associated with the atmospheric synoptic scale. A simple methodology for assessing future levels of air pollutants' concentrations based on synoptic forecasts is presented. At short time scales the methodology is comparable and slightly better than persistence and seasonal forecasts at categorical classification of pollution levels. It's utility is shown for air quality studies at the long time scale of a changing climate scenario, where seasonality and persistence cannot be used. It is demonstrated that the air quality variability due to changes in the pollution emissions can be expected to be much larger than that associated with the effects of climatic changes.

Soil is an important reservoir of PCDD/PCDF, which can be released when environmental conditions change. Fire is an extreme event that can increase the surface temperatures of soil substantially, yet little is known of the role soil plays in the emission of PCDD/PCDF. Soil containing native PCDD/PCDF was fortified with a mixture of mass labelled PCDD/PCDF and heated between 150°C and 400°C. Both native and mass labelled PCDD/PCDF were released from the soil beyond 200°C. Release of the mass labelled compounds was linearly related to temperature with up to 9 % found in the air stream at 400°C. The release of some native PCDD/PCDF was much greater. At 400°C, emission of 1,2,3,7,8-Cl₅DD was 300% compared to pre-experimental soil. Emission of PCDD/PCDF from soil during bushfires is a relevant process and may originate from both volatilization and formation via de novo or precursor pathways, or dechlorination.