Mercury (Hg) is a global toxic pollutant and has raised the world's attention for decades. In this study, we reviewed the fish mercury levels in China (both marine and freshwater, as well as wild and farmed) documented over the past decade and their controlling environmental and biological factors. China is the largest contributor of global Hg cycling and the largest nation for the consumption and export of fish and fish product, thus Hg level in fish becomes a critical issue for food safety and public health. In China, Hg in fish is generally accumulated at a low level, but significant geographical differences were evident and formed the “hot spots” from the north to the south. For marine fish, the east (median: 70 ng g−1 ww, range: 5.0–330 ng g−1 ww) and southeast (median: 72 ng g−1 ww, range: 0.3–329 ng g−1 ww) of China have higher total Hg concentrations than the other coastal areas. For freshwater fish, Tibetan Plateau exhibited the highest total Hg levels (median: 104 ng g−1 ww, range: 5.0–868 ng g−1 ww). Risk assessment of the exposure of low-Hg-level fish to China's population deserves more attention and detailed fish consumption advisories to specific populations are urgently needed. The biokinetic model is a useful tool to characterize the underlying processes involved in Hg accumulation by fish. The diet (Hg concentration, speciation, food quality and quantity) and growth appear to be the important factors affecting the Hg levels of fish in China. The Hg biotransformation can also make contributions to Hg speciation and overall accumulation in fish. The intestinal microbes play an important role in Hg biotransformation and the potential for minimizing Hg contamination in fish deserves further investigation.

Predicting the cotransport of functional microorganisms and heavy metals in porous media is essential to both bioremediation and pollutant risk assessment. In this study, batch and column experiments were conducted to explore the cotransport behaviors of functional bacteria (FA1) and heavy metals (Pb²⁺/Cd²⁺) in saturated sand media under different conditions. The sorption capacity of heavy metals on FA1 was much greater than that of the sand, while both FA1 and sand showed stronger affinity to Pb²⁺ than Cd²⁺. The surface properties, especially zeta potential, of the bacteria and sand were altered by metal adsorption. As a result, the co-existence of Pb²⁺ decreased the transport of FA1 more significantly than that of Cd²⁺, and the influence was more significant with higher heavy metal concentration. On the other hand, the co-existence of FA1 inhibited the mobility of Pb²⁺ and Cd²⁺ in most scenarios, except when the cotransport concentration of Pb²⁺ was 5 mg L⁻¹, and the inhibition was more pronounced for Pb²⁺ than Cd²⁺. Increase in metal concentrations decreased the FA1-associated Pb²⁺/Cd²⁺ in effluents due to the remarkable decrease in FA1 mobility, and free soluble Pb²⁺/Cd²⁺ became the major migration species. In addition, due to stronger attractive forces and affinity between Pb²⁺ and FA1, nearly all presorbed-Pb²⁺ by sand was remobilized by FA1 and transported mainly in FA1-associated form other than soluble Pb²⁺. Findings from this study indicated that the cotransport of biocolloids and heavy metals are highly sensitive to the ion type and concentration, and evaluation of their transport in the subsurface should be carefully carried out to avoid inaccurate estimations.

It is estimated that 10% of the worldwide population lives in the vicinity of an active volcano. However, volcanogenic air pollution studies are still outnumbered when compared with anthropogenic air pollution studies, representing an unknown risk to human populations inhabiting volcanic areas worldwide. This study was carried out in the Azorean archipelago of Portugal, in areas with active non-eruptive volcanism. The hydrothermal emissions within the volcanic complex of Furnas (São Miguel Island) are responsible for the emission of nearly 1000 tons of CO₂ per day, along with H₂S, the radioactive gas – radon, among others. Besides the gaseous emissions, metals (e.g., Hg, Cd, Al, Ni) and particulate matter are also released into the environment. We test the hypothesis that chronic exposure to volcanogenic air pollution alters the histomorphology of the bronchioles and terminal bronchioles, using the house mouse, Mus musculus, as bioindicator species. Mus musculus were live-captured at three different locations: two villages with active volcanism and a village without any type of volcanic activity (reference site). The histomorphology of the bronchioles (diameter, epithelium thickness, smooth muscle layer thickness, submucosa thickness and the histological evaluation of the peribronchiolar inflammation) and of the terminal bronchioles (epithelium thickness and classification) were evaluated. Mice chronically exposed to volcanogenic air pollution presented bronchioles with increased epithelial thickness, increased smooth muscle layer, increased submucosa thickness and increased peribronchiolar inflammation. Similarly, terminal bronchioles presented structural alterations consistent with bronchodysplasia. For the first time we demonstrate that chronic exposure to non-eruptive volcanically active environments causes inflammation and histomorphological alterations in mice lower airways consistent with asthma and chronic bronchitis. These results reveal that chronic exposure to non-eruptive volcanic activity represents a risk factor that can affect the health of the respiratory system of humans inhabiting hydrothermal areas.

High removal efficiency and excellent recyclability are the fundamental qualities that an outstanding adsorbent used for organic dye removal should possess. In this study, two recyclable gels (sodium alginate/Ca/fiber: SCFA hydrogels; cellulose nanofiber/chitosan: CNFCS aerogels) were successfully fabricated using the facile method. Additionally, the as-prepared adsorbents were investigated using a series of characterizations. The adsorption behavior and anti-interference performance of the synthesized gels were compared by choosing methylene blue (MB) as the model pollutant. The kinetic behavior of the gels towards MB was consistent with the pseudo first-order model, and the SCFA hydrogels reached adsorption equilibrium faster than the CNFCS aerogels. The maximum adsorption capacity of MB on the SCFA hydrogels and CNFCS aerogels was 1335.0 and 164.5 mg g⁻¹ (pH = 7.0, dosage: 0.5 g/L; initial concentration from 15 to 180 mg L⁻¹), respectively. More specifically, we found that the co-existing anions had different effects on MB adsorption over the gels used for MB removal. Furthermore, for the SCFA hydrogels, co-existing natural organic matter (NOM) at low concentrations enhanced MB adsorption, and then stabilized as the concentration of NOM increased. However, this increasing trend was not observed for MB adsorption on CNFCS aerogels; these gels exhibited a slight decrease at first, and then showed no change. Nevertheless, both the gels exhibited superior regeneration and recycling abilities.

Airborne lower-chlorinated PCBs are vulnerable to metabolization to PCB sulfates through further sulfation of the hydroxylated metabolites (OH-PCBs). However, studies on the toxic effects and mechanisms of PCB sulfates are still very limited. Here, we investigated for the first time the potential endocrine disruption effects of PCB sulfates through estrogen-related receptor γ (ERRγ) in comparison with their OH-PCBs precursors and PCB parent compounds. The binding affinity of thirteen PCBs/OH-PCBs/PCB sulfates was measured by using fluorescence competitive binding assays based on fluorescence polarization (FP). All of the tested chemicals could bind to ERRγ with the Kd (dissociation constant) values ranging from not available (NA) to 3.2 μM 4′–OH–PCB 12 showed the highest binding affinity with Kd value of 3.2 μM, which was comparable to that of a synthetic ERRγ agonist GSK4716. The effects of the thirteen chemicals on the ERRγ transcriptional activity were determined by using the luciferase reporter gene assay. We found the PCBs/OH-PCBs/PCB sulfates acted as agonists for ERRγ, with the lowest observed effective concentration reaching 3 μM. The binding affinity and agonistic activity of PCBs towards ERRγ were both enhanced after hydroxylation, while further sulfation of OH-PCBs decreased the activity instead. Molecular docking simulation showed that OH-PCBs had lower binding energy than the corresponding PCBs and PCB sulfates, indicating that OH-PCBs had higher binding affinity theoretically. In addition, OH-PCBs could form hydrogen bonds with amino acids Glu316 and Arg247 while PCBs and PCB sulfates could not, which might be the main factor impacting the binding affinity and agonistic activity. Overall, ERRγ is a novel target for lower-chlorinated PCBs and their metabolites.

Mine tailings contain toxic metals and can lead to serious pollutions of soil environment. Phytoremediation using legumes has been regarded as an eco-friendly way for the rehabilitation of tailings-laden lands but little is known about the changes of microbial structure during the process. In the present study, we monitored the dynamic change of microbiota in the rhizosphere of Pongamia pinnata during a 2-year on-site remediation of vanadium-titanium magnetite tailings. After remediation, overall soil health conditions were significantly improved as increased available N and P contents and enzyme activities were discovered. There was also an increase of microbial carbon and nitrogen contents. The Illumina sequencing technique revealed that the abundance of taxa under Proteobacteria was increased and rhizobia-related OTUs were preferentially enriched. A significant difference was discovered for sample groups before and after remediation. Rhizobium and Nordella were identified as the keystone taxa at genus rank. Functional predictions indicated that nitrogen fixation was enhanced, corresponding well with qPCR results which showed a significant increase of nifH gene copy numbers by the 2nd year. Our findings for the first time elucidated that legume phytoremediation can effectively cause microbial communities to shift in favour of rhizobia in heavy metal contaminated soil.

Size-segregated ambient particles down to particles smaller than 0.1 μm (PM₀.₁) were collected during the year 2014–2015 using cascade air samplers with a PM₀.₁ stage, at two cities in Thailand, Bangkok and Chiang Mai. Their characteristics and seasonal behavior were evaluated based on the thermal/optical reflectance (IMPROVE_TOR) method. Diagnostic indices for their emission sources and the black carbon (BC) concentration were assessed using an aethalometer and related to the monthly emission inventory (EI) of particle-bound BC and organic carbon (OC) in order to investigate the contribution of agricultural activities and forest fires as well as agro-industries in Thailand. Monthly provincial EIs were evaluated based on the number of agricultural crops produced corresponding to field residue burning and the use of residues as fuel in agro-industries, and also on the number of hot spots from satellite images corresponding to the areas burned by forest fires. The ratio of char-EC/soot-EC describing the relative influence of biomass combustion to diesel emission was found to be in agreement with the EI of BC from biomass burning in the size range <1 μm. This was especially true for PM₀.₁, which usually tends to be indicative of diesel exhaust particles, and was shown to be very sensitive to the EI of biomass burning. In Chiang Mai, the northern part of Thailand, the forest fires located upwind of the monitoring site were found to be the largest contributor while the carbon behavior at the site in Bangkok was better accounted for by the EI of provinces in central Thailand including Bangkok and its surrounding provinces, where the burning of crop residues and the cultivation of sugarcane for sugar production are significant factors. This suggests that the influence of transportation of polluted air masses is important on a multi-provincial scale (100–200 km) in Thailand.

Tungstate enrichment in aquatic systems may cause negative environmental and health effects. This study addresses tungstate removal from aqueous solution by nanocrystalline iowaite, an iron-bearing layered double hydroxide, which has not been used for treatment of tungstate-rich waters so far. Tungstate sorption experiments were conducted with various contact times, temperatures, initial tungstate concentrations (0.001–2 mM), and solution pH values (2–13), the results indicating that iowaite sorbed aqueous tungstate effectively and quickly, and the sorption maximum can be up to 71.9 mg/g. Moreover, the tungsten sorption capacity keeps nearly constant at a wide pH range from 3 to 11. Duo to its pH buffering effect, the alkaline conditions were generated by the addition of iowaite, which are favorable for the removal of aqueous tungstate because the polymerization of tungstate can be prohibited at alkaline pH values. Zeta potential, XRD and XPS analyses were employed to clarify the sorption mechanisms, and it was concluded that tungstate was sorbed via its exchange with the chloride originally intercalated into iowaite interlayers as well as its stronger inner-sphere complexation with the Fe atoms located in iowaite layers. Nanocrystalline iowaite is suitable for treating both tungstate-bearing natural waters with moderately high tungstate concentrations and industrial wastewaters extremely rich in tungstate.

Tetracycline (TC) can enter the human body via the soil-vegetable-human food chain; therefore, it is necessary to understand the toxicity of TC to humans through vegetables grown on contaminated soils. The present study combined an enzyme-linked immunosorbent assay method and an HL-7702 cell model and assessed the bioavailability and toxicity of TC from pak choi (Brassica campestris L. ssp. chinensis) grown on TC-contaminated soils. The results showed that the degradation rate of TC in black soil was significantly higher than that in purplish clay, while the results for TC uptake in pak choi were opposite. The bioaccessibility of TC was found to be higher in pak choi grown on purplish clay (5.67–7.59%) than in that grown on black soil (5.22–6.77%). It is suggested that soil properties contribute to the uptake of TC by pak choi. More fertile soil contained lower TC concentrations and thus mediated lower TC toxicity to humans. It may seem comforting that TC concentrations in the edible parts of pak choi are often found to be below safe limits. However, the TC diagnosis method showed that even moderate increases in TC concentrations in pak choi may induce oxidative stress, liver injury, mitochondrial cristae and rough endoplasmic reticulum swelling, and early apoptosis in liver cells HL-7702. The pak choi grown in purplish clay showed higher TC cytotoxicity than that grown in black soil. The TC cytotoxicity of raw pak choi was found to be higher than that of cooked pak choi. These results provide direct evidence of effective ways to prevent TC toxicity in humans.

We studied the size distribution of ions (Cl⁻, NO₃⁻, SO₄⁼, Na⁺, NH₄⁺, K⁺, Mg⁺⁺, Ca⁺⁺) and elements (As, Ba, Cd, Co, Cs, Cu, Fe, Li, Mn, Ni, Pb, Rb, Sb, Se, Sn, Sr, Ti, Tl, V, Zn) during the winter and summer seasons of seven consecutive years (2008–2014) in an area of the Po Valley (Northern Italy) characterised by industrial, agricultural and urban settings. The study included the collection and analysis of 41 series of size-segregated samples (MOUDI sampler, 10 stages, cut sizes from 0.18 to 18 μm). Ions were analysed by ion chromatography; elemental analysis was carried out by ICP-MS, by applying a chemical fractionation method able to increase the selectivity of PM source tracers.Our results indicate that important winter/summer variations occurred in both the concentration and size distribution of most PM components. These variations were explained in terms of variations in the strength of the prevailing sources of each component.The contribution of biomass burning for domestic heating was highlighted by the well-known tracer K⁺ but also by the soluble fraction of Rb, Cs and Li. Biomass burning contribution to atmospheric PM was mostly contained in the fine fraction, with a broad size-distribution from 0.18 to 1.8 μm. This source also appreciably increased the concentration of other elements in fine PM (As, Cd, Co, Mn, Pb, Sb, Sn).A few PM components (tracers of sea-spray, brake lining and some industries) did not show marked seasonal variations in concentration and size distribution. However, during winter, for brake lining and industry tracers we observed an upward shift in the dimension of fine particles and a downward shift in the dimension of coarse particles, due to the ageing of the air masses.