Microplastics are an emerging pollutant of high concern, with their prevalence in the environment linked to adverse impacts on aquatic organisms. However, our knowledge of these impacts on freshwater species is rudimentary, and there is almost no research directly testing how these effects can change under ongoing and future climate warming. Given the potential for multiple stressors to interact in nature, research on the combined impacts of microplastics and environmental temperature requires urgent attention. Thus, we experimentally manipulated environmentally realistic concentrations of microplastics and temperature to partition their independent and combined impacts on metabolic and feeding rates of a model freshwater detritivore. There was a significant increase in metabolic and feeding rates with increasing body mass and temperature, in line with metabolic and foraging theory. Experimental warming altered the effect of microplastics on metabolic rate, which increased with microplastic concentration at the lowest temperature, but decreased at the higher temperatures. The microplastics had no effect on the amount of litter consumed by the detritivores, therefore, did not result in altered feeding rates. These results show that the metabolism of important freshwater detritivores could be altered by short-term exposure to microplastics, with greater inhibition of metabolic rates at higher temperatures. The consequences of these metabolic changes may take longer to manifest than the duration of our experiments, requiring further investigation. Our results suggest little short-term impact of microplastics on litter breakdown by gammarid amphipods and highlight the importance of environmental context for a better understanding of microplastic pollution in freshwater ecosystems.

The environmental consequences of nano-CuO particles have gained significant attention in recent decades. Identification of the mechanisms for soil and plant responses with respect to the chemical speciation of nano-CuO (mainly the exchangeable and reducible fractions) remains scarce. Here, we analyzed different chemical speciation of Cu and DTPA-extractable Cu over 42 days in (1) control soil without Cu addition; (2) soil treated with nano-CuO particles; and (3) soil treated with CuSO₄ solution. The applied dose was 500 mg Cu kg⁻¹ and maize was grown in these soils. Plant growth was inhibited, but the inhibition by nano-CuO was slightly weaker compared to CuSO₄. Cu accumulations were similar in the roots for CuSO₄ and nano-CuO treatments, but significantly higher in the shoots for CuSO₄ treatment. This indicates that Cu from nano-CuO-treated soils mainly accumulated in roots but rarely transferred to shoots. Enzyme activities on the rhizoplane visualized by zymography were strongly depressed by CuSO₄ but slightly inhibited by nano-CuO. Microbial community diversity measured by 16S rRNA was the lowest in CuSO₄-treated soils among three treatments. These results were explained by the following mechanisms: (1) Gradual increases of DTPA-extractable and exchangeable Cu were found in nano-CuO-treated soil, and the final concentrations at day 42 were only half of those in CuSO₄-treated soil; (2) Enzyme activities on the rhizoplane were positively related to soil pH and negatively correlated with DTPA-extractable and exchangeable Cu; (3) Even though reducible Cu in nano-CuO-treated soils was 1.3 times higher than in CuSO₄-treated soils, indicating stronger nano-accrued oxidative stress in nano-CuO-treated soils, the toxicity induced by nano-CuO particles was still weaker than CuSO₄. Nevertheless, the toxicity of Cu particles to plants and microbes mainly depends on the gradually-released bioavailable Cu. This demonstrates the greater importance of bioavailable Cu concentrations for toxicity modulation rather than the scale of Cu particles.

The influence of trophic status on the distribution of hydrophobic organic contaminants (HOCs) in different subtropical shallow waters at large spatial scales remains largely unknown. In this study, samples of surface sediments, water, total suspended particles, phytoplankton, and zooplankton were simultaneously collected from 83 sampling sites in 20 subtropical oligotrophic to hyper-eutrophic shallow lakes in China to investigate the influence of trophic status on the spatial distribution and sinking fluxes of 16 polycyclic aromatic hydrocarbons (PAHs). The total concentration of the 16 PAHs (ΣPAH₁₆) in the water columns of these lakes varied from 0.22 to 5.81 μg L⁻¹, and increased with the trophic state index (TSI) and phytoplankton biomass. Phytoplankton were the dominant reservoir for the PAHs in the water column. However, the fraction of ΣPAH₁₆ in phytoplankton decreased with the TSI. The average sinking flux of ΣPAH₁₆ of the individual lakes varied from 2257.1 to 261674.1 mg m⁻² d⁻¹, and increased with the TSI of the lakes. The concentration of ΣPAH₁₆ in the surface sediments ranged from 385.77 to 3784.37 ng gdw⁻¹, and increased with the TSI and the ratio of phycocyanin/sediment organic carbon. It suggested that cyanobacterial biomass affected by trophic status dominated the occurrence of the PAHs in the surface sediments of these lakes. Biomass dilution and the biological pump affected the accumulation of the PAHs in phytoplankton, and zooplankton, and had more influence on the PAHs with higher hydrophobicity. Both the bioconcentration factors and bioaccumulation factors of the PAHs decreased with the TSI. No biomagnification was observed for the PAHs from phytoplankton to zooplankton in these lakes in spring. Our study provided novel knowledge for the coupling between eutrophication and HOCs in 20 subtropical shallow lakes with different trophic status.

The bioremediation potential of an aquifer contaminated with tetrachloroethene (PCE) was assessed by combining hydrogeochemical data of the site, microcosm studies, metabolites concentrations, compound specific-stable carbon isotope analysis and the identification of selected reductive dechlorination biomarker genes. The characterization of the site through 10 monitoring wells evidenced that leaked PCE was transformed to TCE and cis-DCE via hydrogenolysis. Carbon isotopic mass balance of chlorinated ethenes pointed to two distinct sources of contamination and discarded relevant alternate degradation pathways in the aquifer. Application of specific-genus primers targeting Dehalococcoides mccartyi species and the vinyl chloride-to-ethene reductive dehalogenase vcrA indicated the presence of autochthonous bacteria capable of the complete dechlorination of PCE. The observed cis-DCE stall was consistent with the aquifer geochemistry (positive redox potentials; presence of dissolved oxygen, nitrate, and sulphate; absence of ferrous iron), which was thermodynamically favourable to dechlorinate highly chlorinated ethenes but required lower redox potentials to evolve beyond cis-DCE to the innocuous end product ethene. Accordingly, the addition of lactate or a mixture of ethanol plus methanol as electron donor sources in parallel field-derived anoxic microcosms accelerated dechlorination of PCE and passed cis-DCE up to ethene, unlike the controls (without amendments, representative of field natural attenuation). Lactate fermentation produced acetate at near-stoichiometric amounts. The array of techniques used in this study provided complementary lines of evidence to suggest that enhanced anaerobic bioremediation using lactate as electron donor source is a feasible strategy to successfully decontaminate this site.

This study investigates the dynamics of glyphosate and AMPA in the soil surface layer of two fields growing glyphosate-resistant crops in the loess Pampas of Córdoba Province, Argentina. Glyphosate decay and AMPA formation/decay were studied after a single application, using decay kinetic models. Furthermore, glyphosate and AMPA concentrations were investigated in runoff to evaluate their off-site risk. During a 2.5-month study, cultivations of glyphosate-resistant soybean and maize received an application of 1.0 and 0.81 kg a.e. ha⁻¹, respectively, of Roundup UltraMax©. Topsoil samples (0–1, 1–2 cm) were collected weekly (including before application) and analysed for glyphosate, AMPA and soil moisture (SM) contents. Runoff was collected from runoff plots (3 m²) and weirs after 2 erosive rainfall events, and analysed for glyphosate and AMPA contents (water, eroded-sediment). Under both cultivations, background residues in soil before application were 0.27–0.42 mg kg⁻¹ for glyphosate and 1.3–1.7 mg kg⁻¹ for AMPA. In the soybean area, the single-first-order (SFO) model performed best for glyphosate decay. In the maize area, the bi-phasic Hockey-Stick (HS) model performed best for glyphosate decay, due to an abrupt change in SM regimes after high rainfall. Glyphosate half-life and DT₉₀ were 6.0 and 19.8 days, respectively, in the soybean area, and 11.1 and 15.4 days, respectively, in the maize area. In the soybean area, 24% of the glyphosate was degraded to AMPA. In the maize area, it was only 5%. AMPA half-life and DT₉₀ were 54.7 and 182 days, respectively, in the soybean area, and 71.0 and 236 days, respectively, in the maize area. Glyphosate and AMPA contents were 1.1–17.5 times higher in water-eroded sediment than in soil. We conclude that AMPA persists and may accumulate in soil, whereas both glyphosate and AMPA are prone to off-site transport with water erosion, representing a contamination risk for surface waters and adjacent fields.

Biochar has been used to remove heavy metals from aqueous solutions. In this study, a sulfurized wood biochar (SWB) by direct impregnation with elemental sulfur was produced and evaluated along with pristine wood biochar (WB) for adsorption characteristics and mechanism of mercury. Mercury adsorption by WB and SWB was well described by Langmuir model and pseudo second order model and the maximum adsorption capacities of WB and SWB were 57.8 and 107.5 mg g⁻¹, respectively. Intraparticle diffusion model showed that mercury adsorption was fast due to boundary layer and slow adsorption due to diffusion into biochar pores. Although, mercury adsorption by both WB and SWB was predominantly influenced by the pH, temperature, salt concentration, and biochar dosage, the SWB showed a relatively stable mercury adsorption compared to WB under different conditions, suggesting the strong affinity of SWB for mercury. The XPS analysis showed different adsorption mechanisms of mercury between WB and SWB. In particular, mercury adsorption in WB was due to Hg-Cπ bond formation and interaction with carboxyl and hydroxyl groups, whereas in SWB it is primarily due to mercury interaction with C-SOₓ-C and thiophenic groups in addition to Hg-Cπ bond formation and interaction with carboxyl groups. The SEM-EDS mapping also demonstrated that mercury in SWB was related to carbon, oxygen and sulfur. Overall, the sulfurized biochar was effective for removing mercury from aqueous solution, and its direct production through pyrolysis with elemental sulfur impregnation of wood chips could make it an economic option as absorbent for treating mercury-rich wastewater.

The effect of exposure to vinyl chloride monomer (VCM) on susceptibility to hepatotoxicity in children is unknown, although experimental studies have demonstrated a significantly increased risk of hepatocellular carcinoma in rodents exposed to VCM in early life. Epidemiological studies have revealed a high prevalence of liver fibrosis and abnormal liver function in workers exposed to high VCM levels. We aimed to assess the association among urinary thiodiglycolic acid (TDGA) level, abnormal liver function, and hepatic fibrosis in school-aged children living near a petrochemical complex. A total of 303 school-aged (6–13 years) children within 10 km nearly a petrochemical complex was recruited in central Taiwan. First-morning urine and blood samples were collected from each subject, and urinary TDGA level was analyzed through liquid chromatography–tandem mass spectrometry. Liver function was determined by serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. Hepatic fibrosis was assessed using the AST to platelet ratio index (APRI) and fibrosis-4 score (FIB-4). Risk of hepatotoxicity induced by TDGA exposure was estimated using multivariate logistic regression. The median (range, subclinically abnormal %) AST and ALT levels of all subjects were 26.0 (17.0–99.0, 25.7%) and 15.0 (7.0–211.0, 5.9%) IU/L, respectively. Children in the highest urinary TDGA quartile (≥160.0 μg/g creatinine) exhibited significantly elevated median AST levels compared with those in the lowest quartiles (<35.4 μg/g creatinine, p = 0.033). After adjustment for potential confounding factors, children in the highest quartiles (Q₄) of TDGA level had significantly increased odds ratio (OR) of subclinically abnormal AST (OR = 3.86; 95% confidence interval: 1.54–9.67) compared with those in the lowest quartile. A dose-response trend (p = 0.004) was observed. Our findings support the hypothesis that elevated urinary TDGA level in children living near petrochemical complex is associated with susceptibility to hepatotoxicity.

To differentiate the source of aeolian dust between the desert sources from Pan-third pole and high mountain glaciers, therefore, we investigated the spatial variability of aeolian dust sources in the Pan-third polar region. The question of whether such changes reflect variable transport pathways from a unique source in the western China area was addressed. That is, the SrNd radiogenic isotope composition of modern desert samples do not support the hypothesis of a single dust provenance at higher elevation mountain glaciers by long-distance transport; regional sources also play a significant role. Based on previous studies and the data from this study, the five isotopic regions were divided, which are controlled by the geological characteristics in western China. The results suggest that mineral dust deposited into the high-mountain glaciers originated from the free ice region because of glacier melting and the physical and chemical erosion of rocks from the surrounding mountains by local wind systems. The Pb isotopic data further demonstrated that natural dust is the source of Pb for the high-mountain glaciers of Pan-third pole. These results provide an exhaustive documentation of the isotopic signature of the regional dust reaching the glacier regions.

The intentional production and degradation of plastic debris may result in the formation of nanoplastics. Currently, the scarce information on the environmental behaviors of nanoplastics hinders accurate assessment of their potential risks. Herein, the aggregation kinetics of different surface-modified polystyrene nanoparticles in monovalent and divalent electrolytes was investigated to shed some light on the fate of nanoplastics in the aquatic environment. Three monodisperse nanoparticles including unmodified nanoparticles (PS-Bare), carboxylated nanoparticles (PS–COOH) and amino modified nanoparticles (PS–NH₂), as well as one polydisperse nanoparticles that formed by laser ablation of polystyrene films (PS-Laser) were used as models to understand the effects of surface groups and morphology. Results showed that aggregation kinetics of negatively charged PS-Bare and PS-COOH obeyed the DLVO theory in NaCl and CaCl₂ solutions. The presence of Suwannee river natural organic matters (SRNOM) suppressed the aggregation of PS-Bare and PS-COOH in monovalent electrolytes by steric hindrance. However, in divalent electrolytes, their stability was enhanced at low concentrations of SRNOM (below 5 mg C L⁻¹), while became worse at high concentrations of SRNOM (above 5 mg C L⁻¹) due to the interparticle bridging effect caused by Ca²⁺ and carboxyl groups of SRNOM. The cation bridging effect was also observed for PS-laser in the presence of high concentrations of divalent electrolytes and SRNOM. The adsorption of SRNOM could neutralize or even reverse surface charges of positively charged PS-NH₂ at high concentrations, thus enhanced or inhibited the aggregation of PS-NH₂. No synergistic effect of Ca²⁺ and SRNOM was observed on the aggregation of PS-NH₂, probably due to the steric repulsion imparted by the surface modification. Our results highlight that surface charge and surface modification significantly influence aggregation behaviors of nanoplastics in aquatic systems.

Whilst numerous studies have explored the spatial patterns and underlying causes of PM₂.₅, little attention has been paid to the spatial heterogeneity of the factors affecting PM₂.₅. In this study, a geographically weighted regression (GWR) model was used to explore the strength and direction of nexus between various factors and PM₂.₅ in Chinese cities. A comprehensive interpretive framework was established, composed of 18 determinants spanning the three categories of natural conditions, socioeconomic factors, and city features. Our results indicate that PM₂.₅ concentration levels were spatially heterogeneous and markedly higher in cities in eastern China than in cities in the west of the country. Based on the results of GWR, significant spatial heterogeneity was identified in both the direction and strength of the determinants at the local scale. Among all of the natural variables, elevation was found to be statistically significant with its effects on PM₂.₅ in 95.60% of the cities and it correlated negatively with PM₂.₅ in 99.63% cities, with its effect gradually weakening from the eastern to the western parts of China. The variable of built-up areas emerged as the strongest variable amongst the socioeconomic variables studied; it maintained a positive significant relationship in cities located in the Pearl River Delta and surrounding areas, while in other cities it exhibited a negative relationship to PM₂.₅. The highest coefficients were located in cities in northeast China. As the strongest variable amongst the six landscape factors, patch density maintained a positive relationship in part of cities. While in cities in the northeast regions, patch density exhibited a negative relationship with PM₂.₅, revealing that increasing urban fragmentation was conducive to PM₂.₅ reductions in those regions. These empirical results provide a basis for the formulation of targeted and differentiated air quality improvement measures in the task of regional PM₂.₅ governances.