International audience | The environmental presence of mercury has dramatically increased over the past century, leading to increased uptake, especially by top predators such as seabirds. Understanding the exact sources of contamination requires an individual-level approach, which is especially challenging for species that migrate. We took such an approach and located the wintering areas of 80 common terns (Sterna hirundo) through tracking, and, across years, collected feathers grown in those areas to assess their mercury levels using atomic absorption spectrometry. Although feathers of males and females did not differ in their mercury level, we found the average feather mercury level to be highest in birds wintering in the Canary Current (3.87 μg g⁻¹), medium in birds wintering in the Guinea Current (2.27 μg g⁻¹) and lowest in birds wintering in the Benguela Current (1.96 μg g⁻¹). Furthermore, we found considerable inter-annual fluctuations in feather mercury levels, a within-individual repeatability of 41%, that the mercury levels of 17% of feather samples exceeded the admitted toxicity threshold of 5 μg g⁻¹, and that the overall mean concentration of 3.4 μg g⁻¹ exceeded that of other published reports for the species. Further studies therefore should assess whether these levels lead to individual-level carry-over effects on survival and reproductive performance.

International audience | The environmental presence of mercury has dramatically increased over the past century, leading to increased uptake, especially by top predators such as seabirds. Understanding the exact sources of contamination requires an individual-level approach, which is especially challenging for species that migrate. We took such an approach and located the wintering areas of 80 common terns (Sterna hirundo) through tracking, and, across years, collected feathers grown in those areas to assess their mercury levels using atomic absorption spectrometry. Although feathers of males and females did not differ in their mercury level, we found the average feather mercury level to be highest in birds wintering in the Canary Current (3.87 μg g⁻¹), medium in birds wintering in the Guinea Current (2.27 μg g⁻¹) and lowest in birds wintering in the Benguela Current (1.96 μg g⁻¹). Furthermore, we found considerable inter-annual fluctuations in feather mercury levels, a within-individual repeatability of 41%, that the mercury levels of 17% of feather samples exceeded the admitted toxicity threshold of 5 μg g⁻¹, and that the overall mean concentration of 3.4 μg g⁻¹ exceeded that of other published reports for the species. Further studies therefore should assess whether these levels lead to individual-level carry-over effects on survival and reproductive performance.

International audience | Mercury (Hg) is a highly toxic metal that adversely impacts human and wildlife health. The amount of Hg released globally in the environment has increased steadily since the Industrial Revolution, resulting in growing contamination in biota. Seabirds have been extensively studied to monitor Hg contamination in the world’s oceans. Multidecadal increases in seabird Hg contamination have been documented in polar, temperate and subtropical regions, whereas in tropical regions they are largely unknown. Since seabirds accumulate Hg mainly from their diet, their trophic ecology is fundamental in understanding their Hg exposure over time. Here, we used the sooty tern (Onychoprion fuscatus), the most abundant tropical seabird, as bioindicator of temporal variations in Hg transfer to marine predators in tropical ecosystems in response to trophic changes and other potential drivers. Body feathers were sampled from 220 sooty terns, from museum specimens (n=134) and free-living birds (n=86) from Ascension Island, in the South Atlantic Ocean, over 145 years (1876-2021). Chemical analyses included (i) Hg (total- and methyl-Hg), and (ii) carbon (δ¹³C) and nitrogen (δ¹5N) stable isotopes, as proxies of foraging habitat and trophic position, respectively, to investigate the relationship between trophic ecology and Hg contamination over time. Despite current regulations on its global emissions, mean Hg concentrations were 58.9% higher in the 2020s (2.0 µg/g, n=34) than in the 1920s (1.2 µg/g, n=107). Feather Hg concentrations were negatively and positively associated with δ¹³C and δ¹5N values. The sharp decline of 2.9 ‰ in δ¹³C values over time indicates ecosystem-wide changes (shifting primary productivity) in the tropical South Atlantic Ocean and can help explain the observed increase in tern’s feather Hg concentrations. Overall, this study provides invaluable information on how ecosystem-wide changes can increase Hg contamination of tropical marine predators and reinforces the need for long-term regulations of harmful contaminants at the global scale.

International audience | Mercury (Hg) is a toxic contaminant present in most aquatic ecosystems. High concentrations pose serious threats to organisms and to human health. Because previous studies focused on few countries, environmental hazard due to Hg contamination remains obscure in many geographic areas, and for example limited information is available in North Africa. We examined total Hg contamination in 13 sites in Morocco (12 rivers and one lake) spread over a large area, 400 km north–south and 350 km west–east, that encompasses different biogeographic zones separated by the Atlas Mountains. Due to their longevity and sedentary habits, we used freshwater turtles as biological probes to monitor Hg exposure. Keratinized tissues reflect long-term Hg exposure; thus, we assayed Hg concentration in the claws of > 200 individuals and supplemented these data with blood Hg concentrations of > 60 individuals (a tissue that provides shorter term Hg exposure integration). The results provide the first large-scale picture of Hg contamination in the aquatic freshwater systems of Morocco. Comparisons with previous studies revealed that some of the sites were highly contaminated (e.g. mean Hg concentrations were above 5 μg g⁻¹, a very high level in keratinized tissues) whereas other sites presented moderate or baseline levels. Unexpectedly, all highly contaminated sites were found in less densely populated areas, while more densely urbanized northern sites, even the sewers of large cities, were not highly contaminated. We hypothesize that silver mining activities in the southern High Atlas and in the Anti-Atlas contaminate rivers of the catchment basins over long distances. These findings indicate that fish, water consumption and contamination levels in local people should be further scrutinized.

Inhalation represents the most prevalent route of exposure with Thorium-232 compounds (Th-nitrate/Th-dioxide)/Th-containing dust in real occupational scenario. The present study investigated the mechanism of Th response in normal human alveolar epithelial cells (WI26), exposed to Th-nitrate or colloidal Th-dioxide (1–100 μg/ml, 24–72 h). Assessment in terms of changes in cell morphology, cell proliferation (cell count), plasma membrane integrity (lactate dehydrogenase leakage) and mitochondrial metabolic activity (MTT reduction) showed that Th-dioxide was quantitatively more deleterious than Th-nitrate to WI26 cells. TEM and immunofluorescence analysis suggested that Th-dioxide followed a clathrin/caveolin-mediated endocytosis, however, membrane perforation/non-endocytosis seemed to be the mode of Th internalization in cells exposed to Th-nitrate. Th-estimation by ICP-MS showed significantly higher uptake of Th in cells treated with Th-dioxide than with Th-nitrate at a given concentration. Both Th-dioxide and nitrate were found to increase the level of reactive oxygen species, which seemed to be responsible for lipid peroxidation, alteration in mitochondrial membrane potential and DNA-damage. Amongst HSPs, the protein levels of HSP70 and HSP90 were affected differentially by Th-nitrate/dioxide. Specific inhibitors of ATM (KU55933) or HSP90 (17AAG) were found to increase the Th- cytotoxicity suggesting prosurvival role of these signaling molecules in rescuing the cells from Th-toxicity.

Microbial biofilms can rapidly colonize plastic debris in aquatic environments and subsequently, accumulate chemical pollutants from the surrounding water. Here, we studied the microbial colonization of different plastics, including polyethylene terephthalate (PET), polypropylene (PP), polyvinyl chloride (PVC), and polyethylene (PE) exposed in three freshwater systems (the Qinhuai River, the Niushoushan River, and Donghu Lake) for 44 days. We also assessed the biofilm mass and associated metals attached to plastics. The plastics debris characteristics, such as contact angle and surface roughness, greatly affected the increased biofilm biomass. All types of metal accumulation onto the plastic substrate abundances significantly higher than the concentrations of heavy metal in the water column, such as Ba (267.75 μg/g vs. 42.12 μg/L, Donhu Lake), Zn (254 μg/g vs. 0.023 μg/L the Qinhuai River), and Cr (93.75 μg/g vs. 0.039 μg/L, the Niushoushan River). Compared with other metals, the heavy metal Ba, Cr and Zn accumulated easily on the plastic debris (PET, PP, PVC, and PE) at all incubation sites. Aquatic environmental factors (total nitrogen, total phosphorus, and suspended solids concentrations) largely shaped metal accumulation onto plastic debris compared with plastic debris properties.

Piscivorous avian species may be affected by mercury (Hg) which tends to accumulate in aquatic environments and biomagnifies across the food webs. One of such species is the black stork, whose population increase recently slowed down due to unknown reasons. At the same time Hg contamination and its effects were almost unaudited for this species, so it may have exerted deleterious effects on the population and an evaluation is necessary. This is the first study of this species concerning Hg contamination. Thus, Hg concentrations were investigated in the down of black stork chicks (N = 90) from breeding locations in central and southern Poland (Europe) between 2015 and 2017. As well as Hg levels, morphometric parameters and age were evaluated. Mean Hg concentrations reached 0.7 μg/g d.w. and differed significantly between years, from the lowest value noted in 2017 (mean 0.5 μg/g), through 2016 (0.7 μg/g), to the highest one in 2015 (0.9 μg/g), and between nest locations where higher Hg levels were generally found in northern parts of the study area. Hg concentrations were also unrelated to morphometric parameters. Contrarily, morphometric parameters revealed high correlations between themselves, which was confirmed by the cluster analysis (revealing only two clusters) and principal component analysis (the first PC explained 96.8% of the variance). Hg levels in the down of black storks were rather low with the fluctuation between years and nest locations probably caused by parental exposure during wintering, migration, pre-breeding season and recent exposure through food provided by parents. Such low Hg concentrations seemed not to affect the population from the region studied.

The environmental presence of mercury has dramatically increased over the past century, leading to increased uptake, especially by top predators such as seabirds. Understanding the exact sources of contamination requires an individual-level approach, which is especially challenging for species that migrate. We took such an approach and located the wintering areas of 80 common terns (Sterna hirundo) through tracking, and, across years, collected feathers grown in those areas to assess their mercury levels using atomic absorption spectrometry. Although feathers of males and females did not differ in their mercury level, we found the average feather mercury level to be highest in birds wintering in the Canary Current (3.87 μg g⁻¹), medium in birds wintering in the Guinea Current (2.27 μg g⁻¹) and lowest in birds wintering in the Benguela Current (1.96 μg g⁻¹). Furthermore, we found considerable inter-annual fluctuations in feather mercury levels, a within-individual repeatability of 41%, that the mercury levels of 17% of feather samples exceeded the admitted toxicity threshold of 5 μg g⁻¹, and that the overall mean concentration of 3.4 μg g⁻¹ exceeded that of other published reports for the species. Further studies therefore should assess whether these levels lead to individual-level carry-over effects on survival and reproductive performance.

Insufficient evidence exists regarding the effects of microplastics (MPs) on the neuronal toxicity of heavy metals in the early stages of organisms. Herein, the effects of micro-polystyrene (μ-PS; 157 μm) and nano-polystyrene (n-PS; 100 nm) particles on the neurodevelopmental toxicity of mercury (Hg) in zebrafish embryos were compared. Zebrafish embryos exposed to Hg at the concentration of 0.1 mg L⁻¹ revealed blood disorders, delayed hatching, and malformations such as pericardial oedema and tail deformity. The length of the larval head was significantly reduced (P < 0.01) and in vivo expression of atoh1a in the cerebellum of neuron-specific transgenic zebrafish Tg(atoh1a:dTomato) larvae was inhibited by 29.46% under the Hg treatment. Most of the toxic effects were inhibited by the combined exposure to μ-PS or n-PS with Hg, and n-PS decreased the neurodevelopmental toxicity of Hg more significantly than μ-PS. Metabolomic analysis revealed that in addition to inhibiting the amino acid metabolism pathway as in the μ-PS+Hg treatment, the n-PS+Hg treatment inhibited unsaturated fatty acid metabolism in zebrafish larvae, likely because of a greater reduction in Hg bioavailability, thus reducing the oxidative damage caused by Hg in the larvae. The combined effects of MPs and heavy metals differ greatly among different species and their targeted effects. We conclude that the combined toxicity mechanisms of MPs and heavy metals require further clarification.

Maize (Zea mays L.) leaves play an important role in stomatal uptake and surface adsorption of atmospheric mercury (Hg). However, the influence of atmospheric gaseous elemental mercury (GEM) on methylmercury (MeHg) accumulation in maize plants is poorly understood. In this study, we conducted a field open-top chambers (OTCs) experiment and a soil Hg-enriched experiment to investigate the response of MeHg accumulation in maize tissues to different GEM levels in the air. Maize upper leaves had a higher average MeHg concentration (0.21 ± 0.08 ng g⁻¹) than bottom leaves (0.15 ± 0.05 ng g⁻¹) in the OTCs experiment, which was inconsistent with that in the soil Hg-enriched experiment (maize upper leaves: 0.41 ± 0.07 ng g⁻¹, maize bottom leaves: 0.60 ± 0.05 ng g⁻¹). Additionally, significantly positive correlations were found between MeHg concentrations in maize leaves and air Hg levels, suggesting that elevated air Hg levels enhanced MeHg accumulation in maize leaves, which was possibly attributed to methylation of Hg on leaf surfaces. Mature maize grains from the OTCs experiment had low MeHg concentrations (0.12–0.23 ng g⁻¹), suggesting a low accumulation capability of MeHg by maize grains. Approximately 93–96% of MeHg and 51–73% of total Hg in maize grains were lost from the grain-filling stage to the grain-ripening stage at all GEM level treatments, implying that self-detoxification in maize grains occurred. MeHg concentrations in maize roots showed a significant linear relationship (R² = 0.98, p < 0.01) with soil Hg levels, confirming that MeHg in maize roots is primarily from soil. This study provides a new finding that elevated air GEM levels could enhance MeHg accumulation in maize leaves, and self-detoxification may occur in maize grains. Further studies are needed to clarify these mechanisms of Hg methylation on maize leaf surfaces and self-detoxification of Hg by maize grains.