Recent studies have demonstrated the occurrence of microplastic fibers (MFs) in soil environments. To determine whether MFs are harmful for soil biota, we evaluated toxic effects on terrestrial snails (Achatina fulica) after 28 d exposure to polyethylene terephthalate MFs at concentrations of 0.01–0.71 g kg−1 (dry soil weight). Digestion kinetics experiments on 24 snails showed that MFs can be ingested and excreted within 48 h. We found the appearance of cracks and deterioration on the surface of MFs after depuration by the digestive system. Prolonged exposure to 40 snails showed that 0.14–0.71 g kg−1 MFs caused an average reduction of 24.7–34.9% food intake and 46.6–69.7% excretion. 0.71 g kg−1 MFs induced significant villi damage in the gastrointestinal walls of 40% snails, but did not influence the histology of the liver and kidney. Moreover, 0.71 g kg−1 MFs exposure reduced glutathione peroxidase (59.3 ± 13.8%) and total antioxidant capacity (36.7 ± 8.5%), but elevated malondialdehyde level (58.0 ± 6.4%) in the liver, which indicates oxidative stress is involved in the toxic mechanism. Our results suggest that MFs have adverse impacts on the fitness of soil organisms, and highlight the ecological risks of microplastic pollution in terrestrial ecosystems.

We evaluated the short-term effect of mixtures of ambient air pollutants on respiratory and circulatory morbidity in four Colombian cities.Daily Emergency Department (ED) visit records for respiratory and circulatory selected diagnosis and daily concentrations for six criteria air pollutant were obtained in four of the five major cities in Colombia: Bucaramanga, Bogota, Cali, and Medellin during 2011–2014. Using conditional Poisson time series analysis with fixed effects, we assessed the effect of air pollutants on health outcomes using single-pollutant, two-pollutant and specific mixtures-of-pollutant models controlling for meteorology and time trends. The percentages of change in the rate of ED visits and their 95% confidence interval were estimated for the joint effect of pollutants.In single-pollutant models increases in gases concentrations were associated with increases in ED visits for respiratory and circulatory diseases. The two-pollutant models for respiratory diseases showed that the effect of NO₂ alone (% change 2.86 95% CI 1.87–3.85) is higher than the joint effect of any of its combinations except for its combination with SO₂ (% change 3.05 95%CI 1.04–5.05). The two-pollutant models for circulatory diseases showed synergistic effects between NO₂ and PM₂.₅ (% change 2.13 95%CI 0.001–4.26). Specific mixtures models showed that the mixture of “traffic-related pollutants” has the higher joint effect on circulatory morbidity and respiratory morbidity.The results show the dominant effect of NO₂ in air pollution mixtures on respiratory and circulatory morbidity, and the synergistic effect of NO₂ and SO₂ in air pollution mixtures on respiratory morbidity.

It remains a challenge to precisely predict and control environmental behaviors of ionizable organic contaminants (IOCs) due to their species change relative to pH and because of the lack of appropriate models to illustrate the underlying pH-dependent mechanisms. We studied the pH-dependent sorption behavior of five sulfonamide antibiotics (SAs) as typical IOCs with different pKₐ values towards a series of biochars as representative sorbents with well-characterized surface structures. After subtracting the contribution of the speciation effect using a classical speciation model, up to three unexpected enhanced sorption peaks could be found and regulated by the pKₐ,SA of the SAs and the pKₐ, BC of the biochars. The mono H-bond formation between the two pKₐ,SA of the SAs (pKₐ,SA₁ is from NH₂, pKₐ,SA₂ is from SO₂NH), and the biochar surface functional groups with comparable pKₐ values generated two peaks. Another peak around the middle between pKₐ,SA₁ and pKₐ,SA₂ appeared due to the aromatic π bonding-enhanced dual H-bond. All of these peaks were quantitatively separated by a novel two-compartment model, which was developed by capturing the characteristics of pH-dependent sorption. The quantified hydrogen bonding among different SAs elucidates the effectiveness and limits of the pKₐ equalization principle to predict the strengthening of hydrogen bonding at the solid-aqueous interface. This work recognizes the quantitative relationship among the structure, sorption, and H-bond interaction of biochars and guides the prediction of the fate of IOCs in the environment and the development of remediation options.

Several studies have reported associations between exposure to particulate matter and incidence of out-of-hospital cardiac arrest (OHCA) and some have observed associations with ozone (O3). There are no studies investigating susceptibility based on previous disease history to short-term O3 exposure and the risk of OHCA.To investigate the role of previous cardiovascular-related hospitalizations in modifying the associations between the risk of OHCA and short-term increase in O3 concentrations.A time-stratified case-crossover analysis of 11,923 OHCA registered in the Swedish Register for Cardiopulmonary Resuscitation from 2006 to 2014 was performed. Using personal identification numbers, OHCA were linked to all previous hospitalizations in Sweden since 1987 to create susceptible groups based on the principal diagnosis code at discharge. Susceptibility was based on hospitalization for i) acute myocardial infarction; ii) heart failure; iii) arrhythmias; iv) diabetes; v) hypertension; and vi) stroke. Moving 2 and 24-h averages for O3, PM2.5, PM10, and NO2 were constructed from hourly averages.A 10 μg/m3 higher 2-h average O3 concentration was associated with a 2% higher risk of OHCA (95% CI, 0% 3%). Associations were similar for 24-h average O3 and in individuals with or without hospitalizations for AMI, heart failure, diabetes, hypertension or stroke. Individuals with previous hospitalizations for arrhythmias had a lower risk of OHCA with higher O3. No associations were observed for other pollutants.Short-term exposure to O3 was associated with an elevated risk of OHCA, however, previous hospitalizations for cardiovascular diseases were not associated with additionally augmented risks.

Pesticide residues most likely coexist with antibiotics due to the application of animal-based fertilizers in agriculture. In this study, the degradation and enantioselectivity of beta-cypermethrin in soil and chicken manure-amended soil were investigated. The effects of oxytetracycline on the soil microbial community were also estimated. The results showed that the half-life of beta-cypermethrin in the soil was 16.9 days and that the (+)-enantiomer was degraded preferentially in both pairs of enantiomers. The metabolites cis/trans-DCCA(3-(2′,2′-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid) and 3-PBA (3-Phenoxybenzoic acid) were detected. The trans-DCCA concentrations ranged from 0.094 to 0.120 mg/kg, which were higher than the concentrations of cis-DCCA (0.091–0.120 mg/kg) and 3-PBA (0.022–0.061 mg/kg). In the presence of oxytetracycline, beta-cypermethrin degradation was inhibited slightly, while the enantioselectivity was not affected. Oxytetracycline increased the enrichment and persistence of the metabolites. Addition of chicken manure decreased the cis-DCCA residue levels in the soil and alleviated the effect of oxytetracycline; however, chicken manure increased the accumulation and persistence of 3-PBA. In addition, oxytetracycline perturbed the structure of the soil microbial community. The abundance of Proteobacteria increased, while the abundances of Firmicutes and Actinobacteria decreased. These changes might affect the biodegradation of beta-cypermethrin and its metabolites. Combined pollution with antibiotics should be considered for its potential impact on pesticide residues.

Anthropogenic Pb emitted from East Asia, particularly China, is often long-range transported to the east by the prevailing westerlies. To characterize the geographical properties of varying atmospheric Pb concentrations by transboundary and domestic source(s)-related Pb in Korea, closely adjacent to China, the Al and Pb concentrations and the stable Pb isotopic composition were determined in the total suspended particles (TSP) collected at urban (IC), rural (TA), and remote background (JJ) sites in western Korea from August 2015 to October 2016. The annual average Pb concentrations were significantly higher in urban and rural areas (IC, 16.2 ng m⁻³ and TA, 11.1 ng m⁻³) than in remote area (JJ, 6.41 ng m⁻³), showing pronounced seasonal variations with relatively higher concentrations in winter and spring and lower concentrations in summer and autumn. Significantly high enrichment factors (EF) for Pb indicate that anthropogenic contributions are important for this toxic element in TSP. Coupling the Pb isotopic signatures with the air mass back trajectories identified the major potential source regions for individual samples. The results show that during winter, China was the dominant contributor, accounting for 92%, 82%, and 100% of the sampling periods at IC, TA, and JJ, respectively. The Chinese contribution decreased in summer and autumn, whereas the Korean contribution increased, according to the East Asian monsoon system. The Pb concentrations increased by 2.2 (IC), 1.2 (TA) and 1.4 (JJ) times when the Chinese contribution was dominant, compared to the Korea-dominant periods. The Pb isotopic systematics for the samples characterized by the dominant Korean contribution differed substantially between the three sites, implying that the relative importance of various domestic sources varied with geographical areas in western Korea.

Perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic (PFOS) are two perfluorinated chemical products widely existing in the environment. Evidence suggested that PFOA might relate to male reproductive dysfunction in rats and humans. PFOA exposure inhibited the function of Leydig cells. However, it is still unknown whether PFOA affects stem Leydig cells (SLCs). In the present study, we examined the effects of a short-term exposure to PFOA on Leydig cell regeneration and also explored the possible mechanism involved. Thirty-six adult Sprague-Dawley rats were randomly divided into three groups and intraperitoneally injected with a single dose of 75 mg/kg ethane dimethyl sulfonate (EDS) to eliminate all Leydig cells. From post-EDS day 7, the 3 group rats received 0, 25 or 50 mg/kg/day PFOA (n = 12 per group) for 9 consecutive days. Exposure to PFOA significantly decreased serum testosterone levels by day 21 and day 56 post-EDS treatment. Also, the expression levels of Leydig cell specific genes (Lhcgr, Scarb1, Star, Cyp11a1, Hsd3b1, Hsd11b1 and Cyp17a1) and their protein levels were all down-regulated. PFOA exposure may also affect proliferation of SLCs or their progeny since the numbers of PCNA-positive Leydig cells were reduced by post-EDS day 21. These in vivo observations were also confirmed by in vitro studies where the effects of PFOA were tested by culture of seminiferous tubules. In summary, PFOA exposure inhibits the development of Leydig cells, possibly by affecting both the proliferation and differentiation of SLCs or their progeny.

Graphene oxide (GO), used in a wide variety of applications, is increasingly being introduced into aquatic environments; this situation calls for research on GO aggregation and sedimentation to regulate the environmental behaviors and risks. Many studies have investigated the aggregation and the mechanism of GO in water with a single background salt (monosalt system); however, this may not reflect real water environments where multiple salts coexist (multisalt system). A typical synthetic surface water (soft water) with representative multisalts was therefore used to study the aggregation and sedimentation of GO. The GO concentration-dependent aggregation (low concentration aggregation, high concentration stability) was observed in the soft water, and this concentration-dependent aggregation is opposite to the aggregation in monosalt systems (NaCl or CaCl2 solutions). The presence of GO sheets induced the formation of amorphous CaMg(CO3)2 nanoparticles on the GO surfaces in the soft water, and the formed nanoparticles promoted the aggregation and sedimentation of low concentrations of GO through bridging action. Neutral and alkaline conditions were favorable for the formation of CaMg(CO3)2 nanoparticles and the induced GO aggregation. These findings show a new mechanism of GO aggregation in environmentally relevant waters and help us to better evaluate the environmental fate of GO.

The salinization of freshwater environments is a global concern, and one of the largest sources of salinated water is the mining industry. An increasing number of modern mines are working with low grade sulfide ores, resulting in increased volumes of potentially harmful saline drainage. We used water monitoring data, together with data on sedimentary fossil remains (cladoceran, diatom and chironomid), to analyze the spatio-temporal (5 sampling locations and 3 sediment depths) impact of salinated mine water originating from the Talvivaara/Terrafame open cast mine on multiple components of the aquatic ecosystem of Lake Jormasjärvi, Finland. Lake Jormasjärvi is the fourth and largest lake in a chain of lakes along the path of the mine water. Despite the location and large water volume, the mine water has changed the chemistry of Lake Jormasjärvi, reflected in increased electrical conductivity values since 2010. The ecological impact is significant around the inflow region of the lake, as all biological indicator groups show a rapid and directional shift towards new species composition. There is a clear trend in improved water quality as one moves further from the point of inflow, and as one looks back in time. Our results show that salinated mine water may induce rapid and large scale changes, even far downstream along a chain of several sinking basins. This is of special importance in cases where large amounts of waste water are processed in the vicinity of protected habitats.

Due to their low temperatures, the Arctic, Antarctic and Tibetan Plateau are known as the three polar regions of the Earth. As the most remote regions of the globe, the occurrence of persistent organic pollutants (POPs) in these polar regions arouses global concern. In this paper, we review the literatures on POPs involving these three polar regions. Overall, concentrations of POPs in the environment (air, water, soil and biota) have been extensively reported, with higher levels of dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) detected on the Tibetan Plateau. The spatial distribution of POPs in air, water and soil in the three polar regions broadly reflects their distances away from source regions. Based on long-term data, decreasing trends have been observed for most “legacy POPs”. Observations of transport processes of POPs among multiple media have also been carried out, including air–water gas exchange, air–soil gas exchange, emissions from melting glaciers, bioaccumulations along food chains, and exposure risks. The impact of climate change on these processes possibly enhances the re-emission processes of POPs out of water, soil and glaciers, and reduces the bioaccumulation of POPs in food chains. Global POPs transport model have shown the Arctic receives a relatively small fraction of POPs, but that climate change will likely increase the total mass of all compounds in this polar region. Considering the impact of climate change on POPs is still unclear, long-term monitoring data and global/regional models are required, especially in the Antarctic and on the Tibetan Plateau, and the fate of POPs in all three polar regions needs to be comprehensively studied and compared to yield a better understanding of the mechanisms involved in the global cycling of POPs.