Red mud was a highly alkaline hazardous waste, and their resource utilization was a research hotspot. In this study, influencing mechanisms of red mud based passivator on the transformation of Cd fraction in acidic Cd-polluted soil, photosynthetic property, and Cd accumulation in edible amaranth were investigated based on the evaluation of Cd adsorption capacity, root metabolic response, and soil aggregate distribution. Results showed that red mud exhibited good Cd adsorption capacities at about 35 °C and pH 9 in an aqueous solution, and the adsorption behavior of red mud on Cd in rhizosphere soil solution was considered to have some similarity. In the soil-pot trial, red mud application significantly facilitated edible amaranth growth by enhancing the maximum photochemical efficiency and light energy absorption by per unit leaf area by activating more reaction centers. The main mechanisms of rhizosphere soil Cd immobilisation by red mud application included: i) the reduction of mobilized Cd caused by the increasing negative surface charge of soil and precipitation of Cd hydroxides and carbonates at high pH; ii) the increase of organics-Cd complexes caused by the increasing –OH and –COOH amounts adsorbed on the surface of rhizosphere soil after red mud application; and iii) the decrease of available Cd content in soil aggregates caused by the increasing organic matters after red mud application. This study would provide the basis for the safe utilization of red mud remediating acidic Cd-polluted soil.

Thallium (Tl) is a highly toxic metalloid and is considered a priority pollutant by the US Environmental Protection Agency (EPA). Currently, few studies have investigated the distribution patterns of bacterial and fungal microbiomes in Tl-impacted environments. In this study, we used high-throughput sequencing to assess the bacterial and fungal profiles along a gradient of Tl contents in Tl mine waste rocks in southwestern China. Our results showed that Tl had an important, but different influence on the bacterial and fungal diversity indices. Using linear regression analysis, we furtherly divided the dominant bacterial and fungal groups into three distinct microbial sub-communities thriving at high, moderate, and low levels of Tl. Furthermore, our results also showed that Tl is also an important environmental variable that regulates the distribution patterns of ecological clusters and indicator genera. Interestingly, the microbial groups enriched in the samples with high Tl levels were mainly involved in metal and nutrient cycling. Taken together, our results have provided useful information about the responses of bacterial and fungal groups to Tl contamination.

Organosilicons are widely used in consumer products and are ubiquitous in living environments. However, there is little systemic information on this group of pollutants in ambient particles. This study proposes a novel untargeted strategy based mainly on the mass difference of three silicon isotopes to screen organosilicon compounds from 2-year PM₂.₅ samples of Beijing using gas chromatography and high-resolution time-of-flight mass spectrometry. 61 organosilicons were filtered from 1019 peaks, and 35 ones were identified as organosiloxanes including 17 methylsiloxanes and 18 phenylmethylsiloxanes, of which 6 and 3 species were confirmed using reference standards, respectively. These organosiloxanes could be clustered into three groups: low-silicon-number methylsiloxanes, high-silicon-number methylsiloxanes, and phenylmethylsiloxanes. Low-silicon-number methylsiloxanes showed high abundance in the heating season but low abundance in the non-heating season, whereas high-silicon-number methylsiloxanes showed the opposite seasonal variation. This study provides a promising strategy for screening organosilicon compounds through an untargeted approach and gives insights for further investigation of the sources and health risks of organosiloxanes.

In this study, we examined the change rates of PM₂.₅ concentrations, aerosol optical depth (AOD), and the concentrations of PM₂.₅ precursors, such as SO₂ and NO₂, in China and South Korea using surface and satellite observations from 2015 to 2018. To quantify the impacts of the emissions and meteorology on the concentration changes, we performed a series of air quality simulations with year-specific meteorology and a fixed anthropogenic emissions inventory. The surface PM₂.₅ observations in China and South Korea decreased at rates of 9.1 and 4.3%/yr during the study period, respectively. The AODs from Moderate Resolution Imaging Spectroradiometer (MODIS) and Geostationary Ocean Color Imager (GOCI) also decreased faster over China than the AODs over South Korea. For the PM₂.₅ decrease in China, the emission impact was more significant (73%) than the meteorology impact (27%). On the contrary, in South Korea, the emissions and meteorology impacts on PM₂.₅ reductions were similar (51% vs 49%). The SO₂ concentration over China in 2018 significantly reduced to approximately half of the level in 2015. In turn, the sulfate concentration in Baengnyeong (BN), located in a downwind pathway from China to South Korea, decreased at a rate of 0.79%/month. However, the nitrate concentration in BN showed an increasing trend due to the non-linear chemical reactions among sulfate-nitrate-ammonium. The increased nitrate compensated for the reduced PM₂.₅ concentration from the sulfate decrease at BN. Additionally, the number of high (>50 μg/m³) PM₂.₅ concentration days continuously decreased in China, but the number in South Korea increased. It is noted that emission reductions in an upwind area do not guarantee corresponding air quality improvement in the downwind area when complex secondary aerosol formation processes, as well as spatiotemporal changes in meteorology, are involved in the transboundary transport of air pollutants.

The effect of low concentration Cd stress on bivalves is unclear. In this study, Asian clams (Corbicula fluminea) were continuously exposed to 0, 0.05, 0.10, and 0.20 mg/L Cd for 14 d (exposure phase) and to artificial freshwater for 7 d (depuration phase). A total of 16 variables were measured to explore the toxic effects on C. fluminea. All physiological characteristics were significantly inhibited in the treatments (p < 0.05), and the negative effects of Cd did not return to normal levels in the short term. Tissue damage was found in the feet and gills of C. fluminea in all the treatments. On the 7th day (D7), enzyme activity in all the treatments was significantly higher (p < 0.05) than in the control group. Acetylcholinesterase, superoxide dismutase, and catalase activities were enhanced on D14 in all the treatments. However, only glutathione S-transferase activity was significantly higher in all the treatments (p < 0.05) than in the control group on D21. The instability of the enzymes indicated that the adaptability of C. fluminea became stronger throughout the experiment. In each group, the maximum bioaccumulation of Cd followed the order: 0.20 mg/L > 0.05 mg/L > 0.10 mg/L, which might be caused by the filtration capacity of C. fluminea in the 0.05-mg/L group, which was higher than that of the 0.10-mg/L group. Thus, low Cd concentrations effect the physiological characteristics, tissue health, and antioxidant system of C. fluminea and may require a long recovery time to be restored to normal levels.

The presence of higher concentrations of heavy metals in water affects its quality with a concomitant adverse effect on its users thus their removal is paramount. A novel adsorbent, PN-Fe₃O₄-IDA derived from the chemical modification of peanut husk (a low-cost agricultural biomass produced in significant quantities globally) using magnetic nanoparticles (Fe₃O₄) and iminodiacetic acid was utilized for the remediation of heavy metals in aqueous solution. Analytical techniques vis-à-vis the Fourier-Transform Infrared, Scanning Electron Microscope, Brunauer–Emmett–Teller, X-ray photoelectron spectroscopy and X-ray Diffraction were applied for the characterization of PN-Fe₃O₄-IDA. Results from the characterization studies showed that PN-Fe₃O₄-IDA possessed a mesoporous structure, a heterogeneous surface and functional groups such as carboxylic acid and a tertiary nitrogen atom which enhanced its adsorption capacities as well as magnetic properties which ensured its easy removal from the solution using a magnet. The maximum uptake of Pb and Cu onto PN-Fe₃O₄-IDA was 0.36 and 0.75 mmol g⁻¹ (at 318 K) respectively with the chemisorption process being the major reaction pathway for the processes. The synthesized adsorbent exhibits significant adsorption capacity for the selected pollutants as well as some unique features which promotes its use as an adsorbent for wastewater remediation processes.

Environmental impacts associated with mining can be important even after cessation of ore extraction, particularly where sites are abandoned and unremediated. Acid Mine Drainage (AMD) is a common concern in such legacy mines where sulfide ores were extracted. AMD can introduce large concentrations of heavy metals to aquatic systems and contaminate the environment for many kilometres downstream of old mines. Understanding the pattern and history of contamination from legacy mines can help environmental managers make better management decisions. Meta-analysis is a statistical tool that can help determine the significance of changes in metal contamination over the years since cessation of mining. Here we use meta-analysis to examine metal contamination at and downstream of Sunny Corner silver (Ag)-lead (Pb)-zinc (Zn) mine in eastern Australia. Copper (Cu), Zn and Pb concentrations in water increased from 1978 to 2018 within 2 km downstream of the main mine adit, whereas for stream sediment, only Zn concentrations increased significantly over the same period. In contrast, Pb concentrations in surface soil decreased over the years from 2000 to 2018.

Aquatic organisms that inhabit coastal environments are generally exposed to multiple mixtures of chemicals. The single and mixture toxicity of nine trace metals (As, Cd, Cr, Cu, Fe, Hg, Ni, Pb, and Zn) to the rotifer Proales similis were examined at four different salinities (5, 15, 25, and 35 ppt). Chronic toxicity reproductive tests were performed using an application factor (AF) of 0.05, 0.1, 0.2, and 0.4 by multiplying the 24-h LC₅₀ values of each metal. The metal mixture treatments were: T1, As–Cd–Cr–Cu–Fe–Hg–Ni–Pb–Zn; T2, As–Cd–Hg–Pb and; T3, Cr–Cu–Fe–Ni–Zn. The LC₅₀ values ranged between 5 and 4140 μg L⁻¹ in the following order: Hg > Cu > Fe > Pb > Cd > Zn > As > Cr > Ni in low salinity and Hg > Cu > Fe > Pb > Zn > As > Cd > Cr > Ni in high salinity conditions. In all cases, acute toxicity was higher at a salinity of 5 ppt compared to 35 ppt. Chronic toxicity tests indicated that single metal toxicity intensified as the AF increased and as salinity decreased. Regardless of salinity, Pb at 0.4 AF was the most toxic metal. Proales similis evidenced a higher growth in the As treatments (0.1 and 0.2 AF) at 35 ppt compared to controls. Furthemore, the T1 and T2 treatments were the most toxic, and in most cases, they induced a synergistic effect. Antagonism effects were detected in the T3 treatment at 25 and 35 ppt. The present data highlights the importance of the examination of pollution in natural environmental conditions in which many aquatic invertebrates endure.

Urea is one of the most commonly used nitrogen fertilizers in agricultural soil and is easily decomposed by soil urease resulting in ammonium release. The produced ammonium can be volatilized or converted to nitrate, which is susceptible to leaching, leading to groundwater contamination unless used by plants. Hence, it is important to control the release of nitrogen from the urea. Pyroligneous acid inhibited the urease activity and decreased ammonium release up to 80% compared to the control. Amidase including asparaginase and glutaminase is an enzyme that catalyzes hydrolysis of amide group, similar to urease. Therefore, the effect of pyroligneous acid on the inhibition of soil amidase was also tested and the results showed that pyroligneous acid competitively inhibited asparaginase while glutaminase was not inhibited. However, inhibitory effect of pyroligneous acid on asparaginase was negligible compared to the urease. The application of pyroligneous acid with a smaller amount of urea for controlled nitrogen release during Chinese cabbage growth showed that dry biomass and nutrient contents of Chinese cabbage were similar to the case of the conventional urea application. The nitrogen utilization efficiency (NUE) was highest for 33% less amount of urea supply with pyroligneous acid (2.21) compared to conventional treatment (1.81). Consequently, the use of pyroligneous acid with urea enhances nitrogen use efficiency while also protecting environments from non-point source contamination.

In this study, PAHs and their transformed PAH products (TPPs) in road dust were subjected to UV driven photolysis, and then extracted using simultaneous pressurized fluid extraction, and analysed using Shimadzu Triple Quadrupole GC/MS. The results of the analysis were used to investigate the robustness and reliability of 14 existing diagnostic ratios (DRs) and two newly proposed molecular DRs that are relevant for characterizing the sources of PAHs and TPPs. The influence of photolysis on the carcinogenic health risk posed to humans by these hazardous pollutants was then assessed. The findings indicated that the DRs segregated into stable, moderately stable and non-stable classes of source characteristics under the influence of photolysis. Only two of the existing DRs, namely, benzo(a)pyrene/benzo(ghi)perylene (BaP/BghiP) and total index exhibited consistent stability to photolysis, whilst fluoranthene/(fluoranthene + pyrene) (FRT/(FRT+PYR)) showed moderate stability. The two newly proposed DRs, naphthalene/1-nitronaphthalene (NAP/NNAP) and pyrene/(1-nitropyrene + 1-hydroxypyrene) (PYR/(1NPY+HPY)) were found to be highly reliable in post-emission source characterization. The cross-plots of the most stable DRs showed that traffic emissions is the primary source of PAHs, whilst post-emission photolysis is the secondary source of nitro-PAH (NPAH) TPPs. The percent resonance energy thermodynamic stability of the PAH pollutants does not exert any direct influence on the source characteristics of the DRs. Adults are more vulnerable to potential carcinogenic risks as a result of PAH and TPPs photolysis whereas negligible risk exist for children. This study contributes to a more reliable diagnosis of PAH and TPP sources and thus, to the regulatory mitigation of these hazardous pollutants thereby, promoting enhanced protection of human health and the environment.