The aim of this study was to characterize qualitatively and quantitatively the composition of the main rhizodeposits emitted from maize (Zea mays) under Cd stress, in order to discuss their role in Cd availability and tolerance. Maize was grown for 6weeks in sand at four Cd exposure levels (0, 10, 20, and 40M Cd in nutrient solution) and two types of rhizodeposits were collected at the end of cultivation period. Mucilage and other molecules adhering to rhizospheric sand were extracted with a buffer before root exudates were collected by diffusion into water. Total carbon, proteins, amino acids, and sugars were analyzed for both rhizodeposit types and about 40 molecules were identified using GC-MS and LC-MS. Cadmium effect on plant morphology and functioning was slight, but consistent with previous works on Cd toxicity. However, rhizodeposition did tend to be impacted, with a decrease in total carbon, sugars, and amino acids correlating with an increasing Cd content. Such a decrease was not noticeable for proteins in root exudates. These observations were confirmed by the same trends in individual compound contents, although the results were generally not statistically significant. Many of the molecules determined are well-known to modify, whether directly or indirectly, Cd speciation and dynamics in the soil and could play a role in Cd tolerance.

The aim of this study was to characterize qualitatively and quantitatively the composition of the main rhizodeposits emitted from maize (Zea mays) under Cd stress, in order to discuss their role in Cd availability and tolerance. Maize was grown for 6 weeks in sand at four Cd exposure levels (0, 10, 20, and 40 μM Cd in nutrient solution) and two types of rhizodeposits were collected at the end of cultivation period. Mucilage and other molecules adhering to rhizospheric sand were extracted with a buffer before root exudates were collected by diffusion into water. Total carbon, proteins, amino acids, and sugars were analyzed for both rhizodeposit types and about 40 molecules were identified using GC-MS and LC-MS. Cadmium effect on plant morphology and functioning was slight, but consistent with previous works on Cd toxicity. However, rhizodeposition did tend to be impacted, with a decrease in total carbon, sugars, and amino acids correlating with an increasing Cd content. Such a decrease was not noticeable for proteins in root exudates. These observations were confirmed by the same trends in individual compound contents, although the results were generally not statistically significant. Many of the molecules determined are well-known to modify, whether directly or indirectly, Cd speciation and dynamics in the soil and could play a role in Cd tolerance.

[Departement_IRSTEA]Eaux [TR1_IRSTEA]BELCA [ADD1_IRSTEA]Systèmes aquatiques soumis à des pressions multiples | International audience | Perfluorinated and polyfluorinated substances (PFASs) are widely found in freshwater ecosystems because of their resistance to degradation and their ability to accumulate in aquatic organisms. While water temperature controls many physiological processes in fish, knowledge of the effects of this factor on PFAS toxicokinetic is still limited. This study presents experimental results of internal distribution and elimination rates of two perfluorinated acid compounds, namely perfluorooctane sulfonate (PFOS) and perfluorohexane sulfonate (PFHxS) in adult rainbow trout (Oncorhynchus mykiss) exposed to three temperatures. Dietary exposure experiments were conducted at 7 °C, 11 °C, and 19 °C and liver, blood, muscle, brain, and kidney were sampled for analysis. PFOS concentrations were comparable to or exceeded those of PFHxS, while PFHxS was eliminated faster than PFOS, whatever the temperature. Internal distribution changed significantly for both substances when fish were exposed to a range of temperatures from 7 to 19 °C. Indeed, PFOS and PFHxS relative distribution increased in blood, liver, and brain while they decreased in muscle when the water temperature rose. The water temperature variation affected the elimination half-lives, depending on the substances and organs.

Perfluorinated and polyfluorinated substances (PFASs) are widely found in freshwater ecosystems because of their resistance to degradation and their ability to accumulate in aquatic organisms. While water temperature controls many physiological processes in fish, knowledge of the effects of this factor on PFAS toxicokinetic is still limited. This study presents experimental results of internal distribution and elimination rates of two perfluorinated acid compounds, namely perfluorooctane sulfonate (PFOS) and perfluorohexane sulfonate (PFHxS) in adult rainbow trout (Oncorhynchus mykiss) exposed to three temperatures. Dietary exposure experiments were conducted at 7 °C, 11 °C, and 19 °C and liver, blood, muscle, brain, and kidney were sampled for analysis. PFOS concentrations were comparable to or exceeded those of PFHxS, while PFHxS was eliminated faster than PFOS, whatever the temperature. Internal distribution changed significantly for both substances when fish were exposed to a range of temperatures from 7 to 19 °C. Indeed, PFOS and PFHxS relative distribution increased in blood, liver, and brain while they decreased in muscle when the water temperature rose. The water temperature variation affected the elimination half-lives, depending on the substances and organs.

International audience | Fixation reactions reduce the concentration of soluble phosphorus (P) and affect crop growth in alkaline calcareous soils. In lab and greenhouse studies, phosphoric acid (PA) or diammonium phosphate (DAP) were evaluated at various P rates (0, 18, 36 and 54 mg kg−1 soil), either as non-mix (designated as NM-PA and NM-DAP, respectively) or after premixing with farmyard manure (FYM) at 400 mg kg−1 soil (designated as PM-PA and PM-DAP, respectively). The amended soil was incubated at 25 °C and 70% water holding capacity for 7 weeks; thereafter, 32P dynamics were measured using the Freundlich kinetic model. A greenhouse study was also conducted using the same thirteen treatments (as used in incubation experiment) and wheat cultivar (Galaxy 2013) was grown following standard agronomic practices. The results showed that application of PM-PA at the highest rate, which caused maximum change in Pr (ΔPr = 59%) in laboratory condition, also produced maximum P uptake by grain (190.3 mg pot−1) and grain yield (44.1 g pot−1) of wheat in greenhouse experiment. Similarly, regression analysis showed that an increase in Pr values caused a corresponding increase in crop parameters. The results suggested that pre-mixing P fertilizer with FYM could be a viable technique to increase P supply and enhance productivity of wheat in alkaline calcareous soils.

Fixation reactions reduce the concentration of soluble phosphorus (P) and affect crop growth in alkaline calcareous soils. In lab and greenhouse studies, phosphoric acid (PA) or diammonium phosphate (DAP) were evaluated at various P rates (0, 18, 36 and 54 mg kg⁻¹ soil), either as non-mix (designated as NM-PA and NM-DAP, respectively) or after premixing with farmyard manure (FYM) at 400 mg kg⁻¹ soil (designated as PM-PA and PM-DAP, respectively). The amended soil was incubated at 25 °C and 70% water holding capacity for 7 weeks; thereafter, ³²P dynamics were measured using the Freundlich kinetic model. A greenhouse study was also conducted using the same thirteen treatments (as used in incubation experiment) and wheat cultivar (Galaxy 2013) was grown following standard agronomic practices. The results showed that application of PM-PA at the highest rate, which caused maximum change in Pr (ΔPr = 59%) in laboratory condition, also produced maximum P uptake by grain (190.3 mg pot⁻¹) and grain yield (44.1 g pot⁻¹) of wheat in greenhouse experiment. Similarly, regression analysis showed that an increase in Pr values caused a corresponding increase in crop parameters. The results suggested that pre-mixing P fertilizer with FYM could be a viable technique to increase P supply and enhance productivity of wheat in alkaline calcareous soils.

Household consumption has been identified to have an essential role in influencing ultimately the environmental pressures generated by human activities. This study assesses the indirect environmental footprint of the Spanish households applying a combination of consumer expenditure surveys with environmentally extended multi-regional input–output analysis. A total of fourteen environmental impact categories are studied from 2006 to 2015. All the impact categories present a similar trend, particularly affected by the economic crisis. The impacts decreased from 2008 to 2013 and finally slightly started rising again from 2014 to 2015. Results show that the dominant categories influencing the indirect environmental footprint in 2015 are (1) food and beverages, (2) housing, and (3) furnishings. From the intensity perspective, housing, transport, and food and beverages appear to be the most intensive consumption clusters in the Spanish household indirect environmental footprint. In relation to the indirect water impacts embodied in the Spanish households’ imports, the largest amount is from European countries and the highest virtual water (59%) corresponds to food and agriculture, in particular from wheat, fruit, vegetables, and dairy products. The findings obtained in relation to the sources generating indirect impacts from household consumption could aid the implementation of future mitigation policies.

Household consumption has been identified to have an essential role in influencing ultimately the environmental pressures generated by human activities. This study assesses the indirect environmental footprint of the Spanish households applying a combination of consumer expenditure surveys with environmentally extended multi-regional input–output analysis. A total of fourteen environmental impact categories are studied from 2006 to 2015. All the impact categories present a similar trend, particularly affected by the economic crisis. The impacts decreased from 2008 to 2013 and finally slightly started rising again from 2014 to 2015. Results show that the dominant categories influencing the indirect environmental footprint in 2015 are (1) food and beverages, (2) housing, and (3) furnishings. From the intensity perspective, housing, transport, and food and beverages appear to be the most intensive consumption clusters in the Spanish household indirect environmental footprint. In relation to the indirect water impacts embodied in the Spanish households’ imports, the largest amount is from European countries and the highest virtual water (59%) corresponds to food and agriculture, in particular from wheat, fruit, vegetables, and dairy products. The findings obtained in relation to the sources generating indirect impacts from household consumption could aid the implementation of future mitigation policies.

Household consumption has been identified to have an essential role in influencing ultimately the environmental pressures generated by human activities. This study assesses the indirect environmental footprint of the Spanish households applying a combination of consumer expenditure surveys with environmentally extended multi-regional input-output analysis. A total of fourteen environmental impact categories are studied from 2006 to 2015. All the impact categories present a similar trend, particularly affected by the economic crisis. The impacts decreased from 2008 to 2013 and finally slightly started rising again from 2014 to 2015. Results show that the dominant categories influencing the indirect environmental footprint in 2015 are (1) food and beverages, (2) housing, and (3) furnishings. From the intensity perspective, housing, transport, and food and beverages appear to be the most intensive consumption clusters in the Spanish household indirect environmental footprint. In relation to the indirect water impacts embodied in the Spanish households' imports, the largest amount is from European countries and the highest virtual water (59%) corresponds to food and agriculture, in particular from wheat, fruit, vegetables, and dairy products. The findings obtained in relation to the sources generating indirect impacts from household consumption could aid the implementation of future mitigation policies.

Nowadays, environmental pollution by microplastics (<5 mm; MP) is a major issue. MP are contaminating marine organisms consumed by humans. This work studied MP contamination in two bivalve species of commercial interest: blue mussel (Mytilus edulis) and common cockle (Cerastoderma edule) sampled on the Channel coastlines (France). In parallel, 13 plastic additives and 27 hydrophobic organic compounds (HOC) were quantified in bivalves flesh using SBSE-TD-GS-MS/MS to explore a possible relationship between their concentrations and MP contamination levels. MP were extracted using a 10% potassium hydroxide digestion method then identified by μ-Raman spectroscopy. The proportion of contaminated bivalves by MP ranged from 34 to 58%. Blue mussels and common cockles exhibited 0.76 ± 0.40 and 2.46 ± 1.16 MP/individual and between 0.15 ± 0.06 and 0.74 ± 0.35 MP/g of tissue wet weight. Some HOC and plastic additives were detected in bivalves. However, no significant Pearson or Spearman correlation was found between MP loads and plastic additives or HOC concentrations in bivalve tissues for the two species.

Nowadays, environmental pollution by microplastics (<5 mm; MP) is a major issue. MP are contaminating marine organisms consumed by humans. This work studied MP contamination in two bivalve species of commercial interest: blue mussel (Mytilus edulis) and common cockle (Cerastoderma edule) sampled on the Channel coastlines (France). In parallel, 13 plastic additives and 27 hydrophobic organic compounds (HOC) were quantified in bivalves flesh using SBSE-TD-GS-MS/MS to explore a possible relationship between their concentrations and MP contamination levels. MP were extracted using a 10% potassium hydroxide digestion method then identified by μ-Raman spectroscopy. The proportion of contaminated bivalves by MP ranged from 34 to 58%. Blue mussels and common cockles exhibited 0.76 ± 0.40 and 2.46 ± 1.16 MP/individual and between 0.15 ± 0.06 and 0.74 ± 0.35 MP/g of tissue wet weight. Some HOC and plastic additives were detected in bivalves. However, no significant Pearson or Spearman correlation was found between MP loads and plastic additives or HOC concentrations in bivalve tissues for the two species.

Due to the growing concern about the presence of microplastics (MP) in the environment, the number of studies evaluating the toxicity of these small persistent particles on different marine species has increased in recent years. Few studies have addressed their impact on marine phytoplankton, a subject of great concern since they are primary producers of the aquatic food web. The aim of this study is to unravel the cytotoxicity of 2.5 μg mL−1 unlabelled amino-modified polystyrene beads of different sizes (0.5 and 2 μm) on the marine diatom Chaetoceros neogracile. In addition to traditional growth and photosynthesis endpoints, several physiological and biochemical parameters were monitored every 24 h in C. neogracile cells by flow cytometry during their exponential growth (72 h). Dynamic Light Scattering measurements revealed the strong aggregation and the negative charge of the beads assayed in the culture medium, which seemed to minimize particle interaction with cells and potentially associated impacts. Indeed, MP were not attached to the microalgal cell wall, as evidenced by scanning electron micrographs. Cell growth, morphology, photosynthesis, reactive oxygen species levels and membrane potential remained unaltered. However, exposure to MP significantly decreased the cellular esterase activity and the neutral lipid content. Microalgal oil bodies could serve as an energy source for maintaining a healthy cellular status. Thus, MP-exposed cells modulate their energy metabolism to properly acclimate to the stress conditions.

Due to the growing concern about the presence of microplastics (MP) in the environment, the number of studies evaluating the toxicity of these small persistent particles on different marine species has increased in recent years. Few studies have addressed their impact on marine phytoplankton, a subject of great concern since they are primary producers of the aquatic food web. The aim of this study is to unravel the cytotoxicity of 2.5 μg mL⁻¹ unlabelled amino-modified polystyrene beads of different sizes (0.5 and 2 μm) on the marine diatom Chaetoceros neogracile. In addition to traditional growth and photosynthesis endpoints, several physiological and biochemical parameters were monitored every 24 h in C. neogracile cells by flow cytometry during their exponential growth (72 h). Dynamic Light Scattering measurements revealed the strong aggregation and the negative charge of the beads assayed in the culture medium, which seemed to minimize particle interaction with cells and potentially associated impacts. Indeed, MP were not attached to the microalgal cell wall, as evidenced by scanning electron micrographs. Cell growth, morphology, photosynthesis, reactive oxygen species levels and membrane potential remained unaltered. However, exposure to MP significantly decreased the cellular esterase activity and the neutral lipid content. Microalgal oil bodies could serve as an energy source for maintaining a healthy cellular status. Thus, MP-exposed cells modulate their energy metabolism to properly acclimate to the stress conditions.

Seafloor litter has been studied both on the continental shelves (by trawling during 24 years) and in canyons (by ROV) of the French Mediterranean sea Water (FMW). On the continental shelf, mean densities range from 49.63 to 289.01 items/km2. The most abundant categories were plastic, glass/ceramics, metals and textiles. Trend analysis shows a significant increase in plastic quantities during the study period. Plastics accumulate at all depths, with heavier items being found in deeper areas, while the continental slope-break appears as a clean area. The spatial distribution of litter revealed the influence of geomorphologic factors, anthropic activities, shipping route, river inputs. All the canyons are affected by debris but coastal canyons (Ligurian Sea and Corsica) were more impacted than offshore canyons in the Gulf of Lion. The FMW appears to be highly polluted with regard to values found in other areas, but lower than those observed in the Eastern Mediterranean.

Seafloor litter has been studied both on the continental shelves (by trawling during 24 years) and in canyons (by ROV) of the French Mediterranean sea Water (FMW). On the continental shelf, mean densities range from 49.63 to 289.01 items/km². The most abundant categories were plastic, glass/ceramics, metals and textiles. Trend analysis shows a significant increase in plastic quantities during the study period. Plastics accumulate at all depths, with heavier items being found in deeper areas, while the continental slope-break appears as a clean area. The spatial distribution of litter revealed the influence of geomorphologic factors, anthropic activities, shipping route, river inputs. All the canyons are affected by debris but coastal canyons (Ligurian Sea and Corsica) were more impacted than offshore canyons in the Gulf of Lion. The FMW appears to be highly polluted with regard to values found in other areas, but lower than those observed in the Eastern Mediterranean.

In this work, a multi-elemental approach combining Cu and Zn stable isotopes is used to assess the metal contamination evolution in the Loire estuary bulk sediments. Elemental geochemical data indicate an increase of metal concentrations from the beginning of the industrial period peaking in the 1990s, followed by an attenuation of metal contamination inputs to the estuary. Zinc isotope compositions suggest a binary mixing process between Zn derived from terrigenous material and multi-urban anthropogenic sources. Copper isotope systematics indicate a single natural dominant source represented by weathered silicate particles from soils and rocks. This work demonstrates the applicability of Zn isotopes to identify anthropogenic Zn sources in coastal systems, even under a low to moderate degree of contamination. Further studies are required to constrain Cu sources and to elucidate possible effects of grain-size and mineralogy in the Cu isotope composition of sediment in the Loire estuary.

In this work, a multi-elemental approach combining Cu and Zn stable isotopes is used to assess the metal contamination evolution in the Loire estuary bulk sediments. Elemental geochemical data indicate an increase of metal concentrations from the beginning of the industrial period peaking in the 1990s, followed by an attenuation of metal contamination inputs to the estuary. Zinc isotope compositions suggest a binary mixing process between Zn derived from terrigenous material and multi-urban anthropogenic sources. Copper isotope systematics indicate a single natural dominant source represented by weathered silicate particles from soils and rocks. This work demonstrates the applicability of Zn isotopes to identify anthropogenic Zn sources in coastal systems, even under a low to moderate degree of contamination. Further studies are required to constrain Cu sources and to elucidate possible effects of grain-size and mineralogy in the Cu isotope composition of sediment in the Loire estuary.