Rivers play a crucial role in collecting and transporting microplastics. Nonetheless, the degree to which microplastic pollution of freshwaters affects its biota remains understudied. Sampling of wild fishes has so far demonstrated that microplastic ingestion occurs commonly across species with alternate feeding modes, as well as in different environmental compartments. Due to the exploratory nature of many preceding studies, drawing insight about factors driving microplastic ingestion has remained difficult. It continues unknown for instance, what the importance of varying environmental microplastic concentrations is to predict ingestion rates in fish from those areas. Here we show that ingestion rates of microplastic particles (>300 μm) in the benthic round goby from the Rhine river were negligible (1 particle in 417 fish). Among the 535 visually selected putative microplastic fragments, stringent data processing steps to reduce the number of false positives during reference library searches, revealed the importance of taking such steps into account in comparison with other data processing routines. Our observations remained consistent, despite having collected fish from a strongly polluted site of the lower Rhine, which served as contrast to a significantly cleaner site upstream. These results demonstrate that higher environmental microplastic concentrations are not necessarily mirrored by higher ingestion rates in a given fish species.

Endocrine disrupting chemicals (EDCs) are common pollutants in coastal waters. To investigate the estrogen risk of EDCs in the coastal areas of Japan, the Japanese common goby, which is a commonly observed species in these waters, was used as the target fish. Plasma 17β-estradiol (E₂) and vitellogenin (VTG) levels were analyzed and the gonads of fish collected from the Taira River (northern Nagasaki, reference site), Nagasaki Port, and two sites in Tokyo Bay were observed. Abnormal levels (>150 ng/mL, p < 0.05) of plasma VTG and high levels of plasma E₂ were detected in the fish from Nagasaki Port and Tokyo Bay, whereas the levels of both were low in the fish from the Taira River. The target EDCs, including natural estrogen [estrone (E₁), and E₂] and alkylphenols [4-t-octylphenol (4-t-OP), 4-nonylphenol (4-NP), and bisphenol-A (BPA)] in water samples were quantified using gas chromatography tandem mass spectrometry (GC/MS/MS), respectively. It was observed that the E₂-equivalent (EEQ) in Nagasaki Port and Tokyo Bay, which was calculated from the actual EDC measurement value, were almost 20- and 150-fold higher, respectively, than that at the reference site (Taira River, 0.021 ng/L). The EEQs mostly comprised natural estrogen in the sampling sites, although there was some influence of alkylphenols. There was an association between the EEQ and the E₂ in environmental water, suggesting a high estrogen risk in Japan coastal waters. Moreover, the results indicated that abnormal VTG synthesis was induced by environmental estrogen (EE) pollution in Nagasaki Port and Tokyo Bay.

Marine and freshwater plastic pollution is a challenging issue receiving large amounts of research and media attention. Yet, few studies have documented the impact of microplastic ingestion to aquatic organisms. In the Pacific Northwest, Chinook salmon are a culturally and commercially significant fish species. The presence of marine and freshwater microplastic pollution is well documented in Chinook salmon habitat, yet no research has investigated the impacts to salmon from microplastic ingestion. The majority of the marine microplastics found in the Salish Sea are microfibers, synthetic extruded polymers that come from commonly worn clothing. To understand the potential impacts of microfiber ingestion to fish, we ran a feeding experiment with juvenile Chinook salmon to determine if ingested fibers are retained or digestion rates altered over a 10 day digestion period. The experiment was completed in two trials, each consisted of 20 control and 20 treatment fish. Treatment fish were each fed an amended ration of 12 food pellets spiked with 20 polyester microfibers and control fish were fed the same ration without added microfibers. Fish were sampled at day 0, 3, 5, 7, and 10 to assess if fibers were retained in their gastrointestinal tract and to determine the rate of digestion. Fibers for the experiment came from washing a red polyester fleece jacket in a microfiber retention bag. Fibers had a mean length of 4.98 mm. Results showed fish were able to clear up to 94% of fed fibers over 10 days. Differences in mean gastrointestinal mass were not statistically significant at any sampled time between treatment and controls, suggesting that the ingestion of microfibers did not alter digestion rates. Further work is needed to understand if repeated exposures, expected in the environment, alter digestion or food assimilation for growth.

Rice is a major dietary source of the toxic trace metal Cd. Large variation in Cd concentration in rice grain was documented by global and regional surveys, with this variation difficult to predict from soil tests. Even within individual fields, a large spatial variation is often observed but the factors controlling this within-field spatial variation are still poorly understood. In the present study, we used field- and laboratory-based experiments to investigate the effects of a gentle slope gradient within paddy fields (a common farmers’ practice to facilitate water flow from the inlet to the outlet) on Cd availability and grain Cd concentrations in unlimed and limed soils. In our field experiments, a gentle slope resulted in large spatial variations in soil redox potential (Eh) and pH upon soil drainage during rice grain filling. As a result of these variations in Eh and pH, there was a 6- to 7-fold spatial within-field variation in grain Cd concentrations, which were the highest in the irrigation inlet area associated with higher Eh values and the lowest in the outlet area with lower Eh values. Our results highlight that soil Eh, and more importantly, field-moist soil pH during grain filling determine grain Cd concentration and accordingly, incorporating measurements of soil redox status (or water content) and pH of field moist soils (rather than air-dried soils) during grain filling may improve the prediction of grain Cd concentrations. Delaying drainage during grain filling or increasing soil pH by liming is effective in reducing grain Cd accumulation.

Studies of the chemical composition of atmospheric aerosols, rain water and snow in various regions of the globe quite often show the presence of pyridine and a number of its low mass derivatives. Nevertheless, the sources of those compounds in the environment have not yet been established and definitely require elucidation, supported by reliable experimental results. In the present work the chemical composition of peat combustion products as one of the important sources of atmospheric aerosol emission is studied by two-dimensional gas chromatography – high-resolution mass spectrometry with a focus on the detection of pyridine derivatives. Twenty-five compounds of this class were reliably identified and quantified in laboratory experiments on peat burning. Among them 3-hydroxypyridine predominates, while the rest analytes are mostly represented by alkyl derivatives: pyridine, 2-methylpyridine, 3-methylpyridine, 2,5-dimethylpyridine, 2,6-dimethylpyridine, 2-ethylpyridine, lutidines (in order of decreasing concentration). The distribution of these combustion products coincides with that obtained earlier in environmental studies carried out in Arctic, Central Russia and France. The experiments on peat thermal decomposition by pyrolysis GC-MS demonstrated that the maximum concentrations as well as the number of detected analytes were found under conditions of oxygen lack and a temperature of about 500 °C, i.e. characteristic conditions of peat wildfires. The observed levels of pyridines’ emission recalculated on the peat dry weight exceeded 200 mg kg⁻¹. Considering hundreds of millions tons of peat burning in megafires over 20,000 tons of pyridines penetrate the Earth atmosphere annually. The obtained results allow concluding that peat burning may be the major and still underestimated source of pyridine and lower alkylpyridines in the Earth atmosphere.

Epidemiological studies have investigated the associations of bisphenol A (BPA) exposure with hypertension risk or blood pressure levels, but findings are inconsistent. Furthermore, the association between its alternatives bisphenol S and F (BPS and BPF) and hypertension risk are not yet known. We conducted a cross-sectional study in 1437 eligible participants without hypertension-related diseases, with complete data about blood pressure levels, hypertension diagnosis, and urinary bisphenols concentrations. Multivariable logistic and linear models were respectively applied to examine the associations of urinary bisphenols concentrations with hypertension risk and blood pressure levels. The dose-response relationship was explored by the restricted cubic spline model. Compared with the reference group of BPA, individuals in the middle and high exposure group had an adjusted odds ratio (OR) of 1.30 and 1.40 for hypertension, had a 3.08 and 2.82 mm Hg higher systolic blood pressure (SBP) levels, respectively, with an inverted “U” shaped dose-response relationship. Compared with the reference group of BPS, individuals in the second and third tertile had an adjusted OR of 1.49 and 1.48 for hypertension, had a 2.61 and 3.89 mm Hg increased levels of SBP, respectively, with a monotonic curve. No significant associations of BPF exposure with hypertension risk or blood pressure levels were found. BPA and BPS exposure were suggested to be associated with increased hypertension risk and blood pressure levels, with different dose-response relationships. Our findings have important implications for public health but require confirmation in prospective studies.

Inorganic particulate nitrate (p-NO3−), gaseous nitric acid (HNO₃₍g₎) and nitrogen oxides (NOₓ = NO + NO₂), as main atmospheric pollutants, have detrimental effects on human health and aquatic/terrestrial ecosystems. Referred to as the ‘Third Pole’ and the ‘Water Tower of Asia’, the Tibetan Plateau (TP) has attracted wide attention on its environmental changes. Here, we evaluated the oxidation processes of atmospheric nitrate as well as traced its potential sources by analyzing the isotopic compositions of nitrate (δ¹⁵N, δ¹⁸O, and Δ¹⁷O) in the aerosols collected from the Mt. Everest region during April to September 2018. Over the entire sampling campaigns, the average of δ¹⁵N(NO3−), δ¹⁸O(NO3−), and Δ¹⁷O(NO3−) was −5.1 ± 2.3‰, 66.7 ± 10.2‰, and 24.1 ± 3.9‰, respectively. The seasonal variation in Δ¹⁷O(NO3−) indicates the relative importance of O₃ and HO₂/RO₂/OH in NOₓ oxidation processes among different seasons. A significant correlation between NO3− and Ca²⁺ and frequent dust storms in the Mt. Everest region indicate that initially, the atmospheric nitrate in this region might have undergone a process of settling; subsequently, it got re-suspended in the dust. Compared with the Δ¹⁷O(NO3−) values in the northern TP, our observed significantly higher values suggest that spatial variations in atmospheric Δ¹⁷O(NO3−) exist within the TP, and this might result from the spatial variations of the atmospheric O₃ levels, especially the stratospheric O₃, over the TP. The observed δ¹⁵N(NO3−) values predicted remarkably low δ¹⁵N values in the NOₓ of the sources and the N isotopic fractionation plays a crucial role in the seasonal changes of δ¹⁵N(NO3−). Combined with the results from the backward trajectory analysis of air mass, we suggest that the vehicle exhausts and agricultural activities in South Asia play a dominant role in determining the nitrate levels in the Mt. Everest region.

The comparison of fly ash generated from lignite combustion in a thermal power plant Kolubara A (Veliki Crljeni) and bottom and fly ash from coal waste combustion in a semi-industrial fluidized bed boiler (Vinča) was performed as the function of particle size. The average total concentrations of the 16 EPA priority PAHs in ash fractions are 0.49 mg kg⁻¹ of ash (thermal power plant) and 17.48 mg kg⁻¹ of ash (fluidized bed boiler). The sum of 3- and 4-ring PAHs accounts for more than 93% of overall PAHs concentration, and the most abundant among them is fluoranthene.The portions of PAHs groups defined based on their physico-chemical properties, as obtained from quantitative structure-activity relationship (QSAR) models included in the Vega platform, were determined. These portions, emission factors, and benzo[a]pyrene equivalence concentrations were further on used to estimate the potential environmental impact of ash disposal. The PAHs emission factors are higher compared to values in the air pollutant emission inventory guidebook of the cooperative program for monitoring and evaluation of the long-range transmission of air pollutants in Europe (EMEP/EEA). The overall emission factors of 16 PAHs for combustion of lignite and coal waste are determined to be 0.15 and 249.97 mg kg⁻¹ of fuel, respectively. Based on the ratios of benzo[a]pyrene equivalence concentrations of each ash and correspondent fuel, the disposal of fly ash from the cyclone of fluidized bed boiler represents the highest risk to the environment among tested ashes.

Laboratory studies demonstrated that the mussels were good model organisms in revealing microplastics (MPs) uptake and toxicity. However, only limited field study data on the MPs in benthic marine mesoherbivores collected from mangrove forests are currently available. In this study, the MPs in the snails (Ellobium chinense) organs, rather than the shell, from a mangrove forest were dominant fraction (maximum reaching to 60%). Unexpectedly, no significant linear relationships were found between the levels of MPs in the organs of the snails and the levels in the sediment/tidal water. Further studies were done to explore the sources of the MPs in snail organs. MPs in snail organs at both the landward (interior) and seaward (exterior) zones mainly origin from the pore water. Moreover, the MPs found in the snails showed no relevance to the particulate matter (PM) collected from pore water. The findings reported here imply that both the MPs and PM in pore water affect the extent of MPs enter into the organs of benthic marine mesoherbivores collected from mangrove forest.

Nickel and cobalt are essential elements that become toxic at high concentrations. Little is known about nickel and cobalt toxicity in aquatic animals. This study aimed to investigate acute and chronic toxicity of nickel and cobalt in Japanese flounder (Paralichthys olivaceous), with emphasis on oxidative stress reactions, histopathological changes, and differences in gene expression. The lethal concentration for 50% mortality (LC₅₀) in 3 and 8 cm Japanese flounder exposed to nickel for 96 h was found to be 86.2 ± 0.018 and 151.3 ± 0.039 mg/L; for cobalt exposure, LC₅₀ was 47.5 ± 0.015 and 180.4 ± 0.034 mg/L, respectively. Chronic nickel and cobalt exposure caused different degrees of oxidative enzyme activity changes in gill, liver, and muscle tissues. Erythrocyte deformations were detected after acute or chronic exposure to nickel and cobalt. the nickel and cobalt exposure also caused pathological changes such as spherical swelling over other gill patches, rod-like proliferations in the gill patch epithelial cell layer, and disorder in hepatocyte arrangement, cell swelling, and cytoplasm loosening. RNA-Seq indicated that there were 184 upregulated and 185 downregulated genes in the liver of Japanese flounder exposed to 15 mg/L nickel for 28 d. For cobalt, 920 upregulated and 457 downregulated genes were detected. Among these differentially expressed genes, 162 were shared by both nickel and cobalt exposure. In both nickel and cobalt, pathways including fatty acid elongation, steroid biosynthesis, unsaturated fatty acid biosynthesis, fatty acid metabolism, PPAR signaling, and ferroptosis were significantly enriched. Taken together, these results aided our understanding of the toxicity of nickel and cobalt in aquatic animals.