Abandoned nonferrous metal(loid) tailings sites are anthropogenic, and represent unique and extreme ecological niches for microbial communities. Tailings contain elevated and toxic content of metal(loid)s that had negative effects on local human health and regional ecosystems. Microbial communities in these typical tailings undergoing natural attenuation are often very poorly examined. The diversity and inferred functions of bacterial communities were examined at seven nonferrous metal(loid) tailings sites in Guangxi (China), which were abandoned between 3 and 31 years ago. The acidity of the tailings sites rose over 31 years of site inactivity. Desulfurivibrio, which were always coupled with sulfur/sulfide oxidation to dissimilate the reduction of nitrate/nitrite, were specific in tailings with 3 years abandonment. However, genus beneficial to plant growth (Rhizobium), and iron/sulfur-oxidizing bacteria and metal(loid)-related genera (Acidiferrobacter and Acidithiobacillus) were specific within tailings abandoned for 23 years or more. The increased abundance of acid-generating iron/sulfur-oxidizing and metal(loid)-related bacteria and specific bacterial communities during the natural attenuation could provide new insights for understanding microbial ecosystem functioning in mine tailings. OTUs related to Sulfuriferula, Bacillus, Sulfurifustis, Gaiella, and Thiobacillus genera were the main contributors differentiating the bacterial communities between the different tailing sites. Multiple correlation analyses between bacterial communities and geochemical parameters indicated that pH, TOC, TN, As, Pb, and Cu were the main drivers influencing the bacterial community structures. PICRUSt functional exploration revealed that the main functions were related to DNA repair and recombination, important functions for bacterial adaptation to cope with the multi-contamination of tailings. Such information provides new insights to guide future metagenomic studies for the identification of key functions beyond metal-transformation/resistance. As well, our results offers novel outlooks for the management of bacterial communities during natural attenuation of multi-contaminated nonferrous metal(loid) tailings sites.

CuFeO₂/CeO₂ as a novel catalyst was synthesized and its catalytic performance was evaluated for electro-Fenton degradation of acid orange 7 (AO7). It was demonstrated from the characterization results that the rhombohedral structure of CuFeO₂ and face-centered cubic fluorite structure of CeO₂ remained stable after nanocomposite construction. The impact of such operating parameters as pH, current intensity and, catalyst amount was investigated and the optimum conditions (100 mgL⁻¹ AO7, pH 3, 150 mgL⁻¹ CuFeO₂/CeO₂, I: 150 mA) determination led to 99.3% AO7 removal and 79.1% COD removal in 60 min. The introduction of CeO₂ as non-inert support had a significant impact on H₂O₂ electro-generation as an important step in AO7 removal. CuFeO₂/CeO₂ presented negligible metal leaching (iron 4.13%, copper 2.4%, and cerium 0.33%) which could be due to the strong interaction between active species and support. The nanocomposite performed efficiently in salty systems and two samples of real wastewaters due to Brønsted acidity character of ceria, which makes it a potential choice in industrial applications. The good performance of nanocomposite could be the result of the synergistic effect between Fe, Cu, and Ce. Regarding scavenging measurements results, the electro-Fenton process followed the Haber-Weiss mechanism. The by-products detection was performed using GC-MS analysis to propose an acceptable pathway for EF degradation of AO7. The BMG kinetics model (1/b = 0.969 (min) and 1/m = 0.269 (min⁻¹)) was matched with the experimental data and described the kinetics of reaction very well. The catalytic activity of CuFeO₂/CeO₂ almost remained after six cycles. Based on the obtained results, CuFeO₂/CeO₂ using the benefit of the synergistic effect of Ce³⁺ with Fe²⁺ and Cu⁺can be introduced as a promising novel catalyst for the electro-Fenton reaction in wastewater treatment.

Thirteen secondary organic aerosol (SOA) tracers of isoprene, monoterpenes and sesquiterpenes were measured for PM₂.₅ aerosols collected at the summit of Mt. Wuyi (1139 m, a.s.l.), to investigate their seasonality and formation mechanism. Concentrations of the isoprene and monoterpene SOA tracers were much higher in summer than those in other seasons. In contrast, β-caryophyllinic acid was found to be the lowest in summer. Concentrations of those BSOA tracers showed a positive correlation with temperature (R² = 0.52–0.70), and a negative correlation with relative humidity (R² = 0.43–0.78). Moreover, thermodynamic model (i.e., ISORROPIA-II) calculation results showed that acidity conditions are favorable for BSOA formation. Robust linear correlations between the BSOA tracers and anthropogenic pollutants such as SO₂ (R² = 0.53–0.7) and NO₂ (R² = 0.37–0.54) were observed for all the samples, suggesting that SO₂ and NOx can enhance BSOA production in the remote mountain area of southeast China, which is related to an acid-catalyzed heterogeneous chemistry. Moreover, we also found a significant correlation between the concentrations of the BSOA tracers and levoglucosan especially for β-caryophyllinic acid, indicating that biomass burning plumes from the distant lowland regions could influence the production of BSOA in the mountain free troposphere. Our results clearly demonstrated that anthropogenic emissions in China could enhance BSOA formation in the distant mountain regions.

Spiramycin is a widely used macrolide antibiotic and exists at high concentration in production wastewater. A thermal-acid hydrolytic pretreatment using silicotungstic acid (STA) under microwave (MW) irradiation was suggested to mitigate spiramycin from production wastewater. Positive correlations were observed between STA dosage, MW power, interaction time and the hydrolytic removal efficiencies, and an integrative equation was generalized quantitively. Rapid and complete removal 100 mg/L of spiramycin was achieved after 8 min of reaction with 1.0 g/L of STA under 200 W of MW irradiation, comparing to 30.1% by MW irradiation or 15.9% by STA alone. The synergetic effects of STA and MW irradiation were originated from the dissociated-proton catalysis by STA and the dipolar rotation heating effect of MW. STA performed much better than the mineral acid H2SO4 under MW, due to the much stronger Brönsted acidity and higher Hammett acidity. After 8 min, 98.0% of antibacterial potency was also reduced. The m/z 558.8614 fragment (P1) and m/z 448.1323 fragment (P2) were identified as the primary products, which were formed by breaking glucosidic bonds and losing mycarose and forosamine for P1 and further mycaminose moiety for P2. Finally, production wastewater with 433 mg/L of spiramycin was effectively treated using this thermal-acid hydrolytic method. Spiramycin and its antibacterial potency both dropped to 0 after 6 min. The potency drop was supposed from the losing of mycarose and/or forosamine. To decrease both the concentration of spiramycin and its antibacterial potency, combinedly using STA and MW was suggested in this work to break down the structural bonds of the functional groups rather than to destroy the whole antibiotic molecules. It is promising for pretreating spiramycin-contained production wastewater to mitigate both the antibiotic and its antibacterial potency.

A key criterion of the UK Government's policy on sustainable forest management is safeguarding the quality and quantity of water. Forests and forestry management practices can have profound effects on the freshwater environment. Poor forest planning or management can severely damage water resources at great cost to other water users; in contrast good management that restores and maintains the natural functions of woodland can benefit the whole aquatic ecosystem.Forests and forest management practices can affect surface water acidification. Monitoring of water chemistry in ten forest and two moorland acid-sensitive catchments in upland Wales commenced in 1991. The streams were selected to supplement the United Kingdom Upland Waters Monitoring Network (UWMN) with additional examples of afforested catchments. Analysis of 22 years of water chemistry data revealed trends indicative of recovery from acidification. Excess sulphate exhibited a significant coherent decline, accompanied by increases in pH and “charge-balance based” acid neutralising capacity (CB-ANC). Alkalinity and “alkalinity-based” acid neutralising capacity (AB-ANC) exhibited fewer trends, possibily due to the variable responses of the organic - carbonate species to increasing pH in these low alkalinity streams. Whilst total anthropogenic acidity declined, dissolved organic carbon and Nitrate-Nitrogen (NNO₃) concentrations have risen, and the contribution of NNO₃ to acidification has increased.Between-stream variability was analysed using Principal Component Analysis of the trend slopes. Hierarchical clustering of the changes in stream water chemistry indicated three distinct clusters with no absolute distinction between moorland and forest streams. Redundancy analysis was used to test for significant site-specific variables that explained differences in the trend slopes, with rainfall, crop age, base cation concentration and forest cover being significant explanatory variables.

Pyrite weathering often occurs in nature and causes heavy metal ion pollution and acid mine drainage during the process. Humic acid (HA) is a critical natural organic material that can bind metal ions, thus affecting metal transfer and transformation. In this work, in situ electrochemical techniques combined with spectroscopic analysis were adopted to investigate the interfacial processes involved in pyrite weathering with/without HA. The results showed that the pyrite weathering mechanism with/without HA is FeS₂ → Fe²⁺ + 2S⁰ + 2e⁻. The presence of HA did not change the pyrite weathering mechanism, but HA adsorbs on the pyrite surface and inhibits the further transformation of sulfur. Furthermore, HA and Fe(II) ions can form complex at 45.0 °C. Increased concentration of HA, decreased HA solution acidity or decreased environmental temperature would all weaken the pyrite weathering, for the above conditions cause pyrite weathering to have a larger resistance of the double layer and a larger passive film resistance. Pyrite will release 73.7 g m⁻²·y⁻¹ Fe²⁺ to solution at pH 4.5, and the amount decreases to 36.8 g m⁻²·y⁻¹ in the presence of 100 mg/L HA. This study provides an in situ electrochemical method for the assessment of pyrite weathering.

Historical increases in emissions and atmospheric deposition of oxidized and reduced nitrogen (N) provided the impetus for extensive, global-scale research investigating the effects of excess N in terrestrial and aquatic ecosystems, with several regions within the Eastern Deciduous Forest of the United States found to be susceptible to negative effects of excess N. The Clean Air Act and associated rules have led to decreases in emissions and deposition of oxidized N, especially in eastern U.S., representing a research challenge and opportunity for ecosystem ecologists and biogeochemists. The purpose of this paper is to predict changes in the structure and function of North American forest ecosystems in a future of decreased N deposition. Hysteresis is a property of a system wherein output is not a strict function of corresponding input, incorporating lag, delay, or history dependence, particularly when the response to decreasing input is different from the response to increasing input. We suggest a conceptual hysteretic model predicting varying lag times in recovery of soil acidification, plant biodiversity, soil microbial communities, forest carbon (C) and N cycling, and surface water chemistry toward pre-N impact conditions. Nearly all of these can potentially respond strongly to reductions in N deposition. Most responses are expected to show some degree of hysteresis, with the greatest delays in response occurring in processes most tightly linked to “slow pools” of N in wood and soil organic matter. Because experimental studies of declines in N loads in forests of North America are lacking and because of the expected hysteresis, it is difficult to generalize from experimental results to patterns expected from declining N deposition. These will likely be long-term phenomena, difficult to distinguish from other, concurrent environmental changes, including elevated atmospheric CO₂, climate change, reductions in acidity, invasions of new species, and long-term vegetation responses to past disturbance.

The high acidity of mercury ions (Hg²⁺) contained wastewater can complicate its safe disposal. MgAl-LDHs supported [SnS₄]⁴⁻ clusters were synthesized for Hg²⁺ removal from acid wastewater. The active sites of [SnS₄]⁴⁻ clusters were inserted into the interlayers of MgAl-LDHs using an ion-exchange method. The experimental results indicated that [SnS₄]⁴⁻/MgAl-LDHs composite can obtain higher than 99% Hg²⁺ removal efficiency under low pH values. The maximum mercury adsorption capacity is 360.6 mg g⁻¹. It indicated that [SnS₄]⁴⁻ clusters were the primary active sites for mercury uptake, existing as stable Hg₂(SnS₄) on the surface of the composite. Under low pH values, such a composite seems like a “net” for HgSO₄ molecules, exhibiting great potential for mercury removal from acid solutions. Moreover, the co-exist metal ions such as Zn²⁺, Na⁺, Cd²⁺, Cr³⁺, Pb²⁺, Co²⁺, and Ni²⁺ have no significant influences on Hg²⁺ removal. The adsorption isotherms and kinetics were also studied, indicating that the adsorption mechanism follows a monolayer chemical adsorption model. The [SnS₄]⁴⁻/MgAl-LDHs composite exhibits a great potential for Hg²⁺ removal from acid wastewater.

In this study, some different selected plant leaves grown in Jordan such as Citrus limon (Rutaceae), Ceratonia siliqua L., Olea europaea (Oleaceae), Washingtonia filifera, and Myoporum (Myoporaceae) were examined for removal of copper (Cu) and zinc (Zn) ions from aqueous solutions. Cu and Zn were analyzed by atomic absorption spectrometry. A pH S-2 acidometer was used for determining the acidity of leaves solution system. Our findings showed the plants leaves were relatively efficient for removal of Cu and Zn compared to activated carbon. Removal of a 5 mg/L aqueous metal solution of Cu and Zn was treated with 2.5 g oven-dried plant in a 50 mL deionized water. The removal of Cu and Zn was expressed in terms of a time function ranged between 0 and 192 hours of contact time. The uptake of Cu and Zn by plant leaves was arranged in the following order:(i)Cu: Activated carbon > Washingtonia filifera > Ceratonia siliqua L. > Olea europaea (Oleaceae) > Myoporum (Myoporaceae) > Citrus limon (Rutaceae)(ii)Zn: Activated carbon > Olea europaea (Oleaceae) > Citrus limon (Rutaceae) > Ceratonia siliqua L. > Washingtonia filifera > Myoporum (Myoporaceae)

Chengdu, the capital city of Sichuan Province, is one of the most polluted cities in China. We used single-particle aerosol mass spectrometer to monitor particulate matter pollution in an urban area of Chengdu from December 9, 2015 to January 4, 2016 to determine the characteristics of air pollution during the winter months. The mass concentrations of particulate matter were high during the whole observation period, with mean values for PM₂.₅ and PM₁₀ of 101 ± 60 and 162 ± 99 μg m⁻³, respectively. The particles were clustered into nine distinct particle types: dust (3%), potassium-elemental carbon (KEC) (24%), organic carbon (OC) (12%), combined OC and EC (OCEC) (6%), K-organic nitrogen (KCN) (10%), K-nitrate (KNO₃) (12%), K-sulfate (KSO₄) (18%), K-sulfate and nitrate (KSN) (12%), and metal (3%) particles. Analysis on different types of day showed that: (1) from “excellent” (days with PM₂.₅ lower than 35 μg m⁻³) to “light pollution” (PM₂.₅ between 75 and 115 μg m⁻³) days, local/regional combustion was the major contributor, whereas the aggravation of pollution from light pollution to “heavy pollution” (PM₂.₅ higher than 150 μg m⁻³) days was mainly determined by the combined effect of local/regional combustion and long-distance transport; (2) as the air quality deteriorated, the mixing of sulfate and nitrate in particles increased sharply, especially sulfate; and (3) the relative aerosols acidity increased from excellent to light pollution days, while decreased significantly from light pollution to heavy pollution days. Backward trajectory analysis showed that there were significant differences in PM₂.₅ concentrations and particle compositions between clusters of trajectories, which affected the level and evolution of PM₂.₅ pollution in Chengdu. These results give a deeper understanding of PM₂.₅ pollution in Chengdu and the Sichuan Basin.