Combined impact of antibiotics and Cr(VI) on antibiotic resistance, ARGs, and growth of Bacillussp. SH-1: A functionl analysis from gene to protease.

The simultaneous selection of antibiotic resistance genes (ARGs) induced by heavy metals and antibiotics has emerged as a growing environmental problem. This study investigated the combined effects of chromium (Cr(VI)) and antibiotics on the ARGs of Bacillus cereus SH-1. As Cr(VI) concentration increased, it triggered reactive oxygen species oxidative stress in SH-1, increased antioxidant enzyme activity, enhanced plasmid conjugative transfer, and reduced the efficiency of Cr(VI) removal by SH-1. Antibiotic resistance varied with increasing tetracycline and amoxicillin minimum inhibitory concentrations (MICs), whereas azithromycin and chloramphenicol MICs decreased with Cr(VI) induction. The overexpression of eight genes of the HAE-1 family of efflux pumps was detected using metagenomics and proteomics. Co-contamination with Cr(VI) and antibiotics has led to the emergence and spread of antibiotic-resistant bacteria. Therefore, resistance gene contamination resulting from Cr(VI)-polluted environments cannot be overlooked.

Bio-stabilization of arsenic in sediments by natural carbon-containing biomass: Performance and microbial metabolites.

The development of sustainable methods for the control and bio-stabilization of arsenic in sediments, without generating secondary pollution, is an urgent technological need. In this study, we utilized three types of natural carbon-containing biomass (NCCB) to explore the stabilization of arsenic through the synergistic action of native sediment microbiomes. We also examined the metabolic pathways of microorganisms following the introduction of NCCB into high-arsenic sediments, aiming to elucidate the biological processes critical for arsenic bio-stabilization. Our findings indicate that humic acid (HA) and soil organic matter (SOM) are effective in preventing the leaching of As(III) from sediments, while fulvic acid (FA) and SOM can significantly reduce the leaching of As(V). Furthermore, the introduction of NCCB into the system altered the biological metabolic processes, with notable upregulation of metabolites such as 8-hydroxyondansetron, 1,2,3,5,6,8-hexathionane, and citric acid. These results hold promise for the application of these findings in the management of arsenic in natural sediments.

Cellulose-based aerogel derived N, B-co-doped porous biochar for high-performance CO2 capture and supercapacitor.

The remarkable characteristics of porous biochar have generated significant interest in various fields, such as CO2 capture and supercapacitors. The modification of aerogel-derived porous biochar through activation and heteroatomic doping can effectively enhance CO2 adsorption and improve supercapacitor performance. In this study, a novel N, B-co-doped porous biochar (NBCPB) was synthesized by carbonating and activating the N, B dual-doped cellulose aerogel. N and B atoms were doped in-situ using a modified alkali-urea method. The potassium citrate was served as both an activator and a salt template to facilitate the formation of a well-developed nanostructure. The optimized NBCPB-650-1 (where 650 corresponded to activation temperature and 1 represented mass ratio of potassium citrate activator to carbonized NBCPB-400 precursor) displayed the largest micropore volume of 0.40 cm3·g-1 and a high specific surface area of 891 m2·g-1, which contributed to an excellent CO2 adsorption capacity of 4.19 mmol·g-1 at 100 kPa and 25 °C, a high CO2/N2 selectivity, and exceptional reusability (retained >97.5 % after 10 adsorption-desorption cycles). Additionally, the NBCPB-650-1 electrode also delivered a high capacitance of 220.9 F·g-1 at 1 A·g-1. Notably, the symmetrical NBCPB-650-1 supercapacitor exhibited a high energy density of 9 Wh·kg-1 at the power density of 100 W·kg-1. This study not only presents the potential application of NBCPB-650-1 material in CO2 capture and electrochemical energy storage, but also offers a new insight into easy-to-scale production of heteroatomic-modified porous biochar.

Synergistic preparation and application in PCU of α-calcium sulfate hemihydrate whiskers from phosphogypsum and electrolytic manganese residue.

The α-calcium sulfate hemihydrate whiskers (α-CSHWs) were first prepared using phosphogypsum (PG) and electrolytic manganese residue (EMR) as raw materials for coating urea, demonstrating excellent controlled-release properties. The effects of different reaction conditions on α-CSHWs, achieved by optimizing the reaction time, the concentrations of NH4+, Mn2+, and other factors, were discussed. Results showed that when the EMR content was 25 wt%, the reaction temperature was 100 °C, and the reaction time was 3 h, α-CSHWs with a length-to-diameter ratio of 39 were obtained. Through experiments and density functional theory (DFT), the mechanism of α-CSHWs preparation was elucidated. The results show that the addition of EMR reduces the content of impurity ions PO43- and F- in PG while introducing NH4+ and Mn2+. Interestingly, both NH4+ and Mn2+ can reduce the nucleation time of α-CSHWs, while PO43-, Mn2+, and F- are more likely to adsorb on the (0 0 6) crystal plane of α-CSHWs, NH4+ readily adsorbs on the (4 0 0) crystal plane. The controlled-release performance of modified α-CSHWs incorporated into polyurethane-coated urea (PCU) was investigated, and it was found that the addition of Mα significantly prolonged the nutrient release period, with the period extending up to 116 days for coatings of 5wt% and above. This work not only enhances the efficiency of PG and EMR utilization but also serves as a reference for the straightforward synthesis and application of α-CSHWs.

Effects of bed depths and the ratio of aerobic to anaerobic zone on the performance of horizontal subsurface flow macrophyte-assisted high-rate vermifilters treating synthetic brewery wastewater.

Effects of total vermibed depth, as well as the ratio of aerobic (the unsubmerged) to anaerobic (the submerged) zone on the performance of the horizontal subsurface flow macrophyte-assisted vermifilters (HSSF-MAVFs) treating synthetic brewery wastewater at a higher hydraulic loading rate (HLR), were investigated for the first time. Results showed that the HSSF-MAVF with a 50 cm total and 18 cm submerged vermibed depth yielded the optimum removal of the pollutants, ensuring a (91.2 ± 1.7)%, (81.8 ± 1.9)%, (67.4 ± 3.9)%, and (63.1 ± 2.3)% removal of chemical oxygen demand (COD), ammonium N (NH4 + -N), total N (TN), and organic N, respectively, whereas there was an increase of (142 ± 6.3)% in the effluent nitrate-N (NO3 - -N) than that in the influent. At the optimum condition, the effluent concentrations of all the pollutants including COD, NH4 + -N, NO3 - -N, TN, and organic N were well below the surface water discharge standards specified by the Central Pollution Control Board (CPCB), and thus, the effluent of the HSSF-MAVF could be safely discharged into the surface water bodies. PRACTITIONER POINTS: Total vermibed depth of HSSF-MAVFs was optimized for organic and nitrogen removal. HSSF-MAVFs were subjected to the higher HLR of synthetic brewery wastewater. Removal of COD and NH4 + -N was decreased with the increase in submerged bed depth. Removal of organic N and TN was increased with the increase in submerged bed depth. Total/unsubmerged bed depth had a positive impact on the organic and N removal.

Changes of MRGs and ARGs in Acinetobacter sp. SL-1 used for treatment of Cr(VI)-contaminated wastewater with waste molasses as carbon source.

Antibiotic resistance genes (ARGs) may be synergistic selected during bio-treatment of chromium-containing wastewater and causing environmental risks through horizontal transfer. This research explored the impact of self-screening bacterium Acinetobacter sp. SL-1 on the treatment of chromium-containing wastewater under varying environmental conditions. The findings indicated that the optimal Cr(VI) removal conditions were an anaerobic environment, 30 °C temperature, 5 g/L waste molasses, 100 mg/L Cr(VI), pH = 7, and a reaction time of 168 h. Under these conditions, the removal of Cr(VI) reached 99.10 %, however, it also developed cross-resistance to tetracycline, gentamicin, clarithromycin, ofloxacin following exposure to Cr(VI). When decrease Cr(VI) concentration to 50 mg/L at pH of 9 with waste molasses as carbon source, the expression of ARGs was down regulated, which decreased the horizontal transfer possibility of ARGs and minimized the potential environmental pollution risk caused by ARGs. The study ultimately emphasized that the treatment of chromium-containing wastewater with waste molasses in conjunction with SL-1 not only effectively eliminates hexavalent chromium but also mitigates the risk of environmental pollution.

Janus Zn-IV-VI: Robust Photocatalysts with Enhanced Built-In Electric Fields and Strain-Regulation Capability for Water Splitting.

The use of 2D materials to produce hydrogen (H2 ) fuel via photocatalytic water splitting has been intensively studied. However, the simultaneous fulfillment of the three essential requirements-high photon utilization, rapid carrier transfer, and low-barrier redox reactions-for wide-pH-range production of H2 still poses a significant challenge with no additional modulation. By employing the first-principles calculations, it has been observed that the Janus ZnXY2 structures (X = Si/Ge/Sn, Y = S/Se/Te) exhibit significantly enhanced built-in electric fields (0.20-0.36 eV Å-1 ), which address the limitations intrinsically. Compared to conventional Janus membranes, the ductile ZnSnSe2 and ZnSnTe2 monolayers have stronger regulation of electric fields, resulting in improved electron mobility and excitonic nature (Ebinding = 0.50/0.35 eV). Both monolayers exhibit lower energy barriers of hydrogen evolution reaction (HER, 0.98/0.86 eV, pH = 7) and resistance to photocorrosion across pH 0-7. Furthermore, the 1% tensile strain can further boost visible light utilization and intermediate absorption. The optimal AC-type bilayer stacking configuration is conducive to enhancing electric fields for photocatalysis. Overall, Janus ZnXY2 membranes overcome the major challenges faced by conventional 2D photocatalysts via intrinsic polarization and external amelioration, enabling efficient and controllable photocatalysis without the need for doping or heterojunctions.

Spatiotemporal-based automated inundation mapping of Ramsar wetlands using Google Earth Engine.

Wetlands are one of the most critical components of an ecosystem, supporting many ecological niches and a rich diversity of flora and fauna. The ecological significance of these sites makes it imperative to study the changes in their inundation extent and propose necessary measures for their conservation. This study analyzes all 64 Ramsar sites in China based on their inundation patterns using Landsat imagery from 1991 to 2020. Annual composites were generated using the short-wave infrared thresholding technique from June to September to create inundation maps. The analysis was carried out on each Ramsar site individually to account for its typical behavior due to regional geographical and climatic conditions. The results of the inundation analysis for each site were subjected to the Mann-Kendall test to determine their trends. The analysis showed that 8 sites exhibited a significantly decreasing trend, while 14 sites displayed a significantly increasing trend. The accuracy of the analysis ranged from a minimum of 72.0% for Hubei Wang Lake to a maximum of 98.0% for Zhangye Heihe Wetland National Nature Reserve. The average overall accuracy of the sites was found to be 90.0%. The findings emphasize the necessity for conservation strategies and policies for Ramsar sites.

Ti-doped iron phosphide nanoarrays grown on carbon cloth as a self-supported electrode for enhanced electrocatalytic nitrogen reduction.

The electrocatalytic nitrogen reduction reaction (eNRR) has been widely recognized as a promising method for green ammonia synthesis. However, the inert NN bond, inferior catalytic activity and small electrochemically active area impede its practical application. To circumvent these problems, we proposed self-supported Ti-doped iron phosphide (FeP) nanorod arrays grown on carbon cloth (Ti-FeP/CC) as an electrode for eNRR. The introduction of Ti doping sites regulated the electron structure of FeP, leading to electron migration from Fe to P, which facilitated N2-to-NH3 conversion. The as-prepared Ti-FeP/CC showed an enhancement of electrochemical surface area (ECSA), high electrical conductivity and well-exposed active sites. Ti-FeP/CC was capable of producing a high NH3 yield of 10.93 µg h-1 cm-2 and faradaic efficiency of 10.77% at an optimal voltage of -0.3 V (vs. RHE) in a 0.1 M Na2SO4 solution with excellent stability and durability during the eNRR process. This work not only presents a promising electrode material for eNRR, but also provides a new insight into rational heteroatom doping for electrocatalysis.

Hierarchical Ni-Mn LDHs@CuC2O4 Nanosheet Arrays-Modified Copper Mesh: A Dual-Functional Material for Enhancing Oil/Water Separation and Supercapacitors.

The pursuit of superhydrophilic materials with hierarchical structures has garnered significant attention across diverse application domains. In this study, we have successfully crafted Ni-Mn LDHs@CuC2O4 nanosheet arrays on a copper mesh (CM) through a synergistic process involving chemical oxidation and hydrothermal deposition. Initially, CuC2O4 nanosheets were synthesized on the copper mesh, closely followed by the growth of Ni-Mn LDHs nanosheets, culminating in the establishment of a multi-tiered surface architecture with exceptional superhydrophilicity and remarkable underwater superoleophobicity. The resultant Ni-Mn LDHs@CuC2O4 CM membrane showcased an unparalleled amalgamation of traits, including superhydrophilicity, underwater superoleophobicity, and the ability to harness photocatalytic forces for self-cleaning actions, making it an advanced oil-water separation membrane. The membrane's performance was impressive, manifesting in a remarkable water flux range (70 kL·m-2·h-1) and an efficient oil separation capability for both oil/water mixture and surfactant-stabilized emulsions (below 60 ppm). Moreover, the innate superhydrophilic characteristics of the membrane rendered it a prime candidate for deployment as a supercapacitor cathode material. Evidenced by a capacitance of 5080 mF·cm-2 at a current density of 6 mA cm-2 in a 6 M KOH electrolyte, the membrane's potential extended beyond oil-water separation. This work not only introduces a cutting-edge oil-water separation membrane and supercapacitor electrode but also offers a promising blueprint for the deliberate engineering of hierarchical structure arrays to cater to a spectrum of related applications.

Remediation of arsenic contaminated water and soil using mechanically (ball milling) activated and pyrite-amended electrolytic manganese slag.

With the development of industry, heavy metal (HM) pollution of soil has become an increasingly serious problem. Using passivators made of industrial by-products to immobilize HMs in contaminated soil is a promising in-situ remediation technology. In this study, the electrolytic manganese slag (EMS) was modified into a passivator (named M-EMS) by ball milling, and the effects of M-EMS on adsorption of As(V) in aquatic samples and on immobilization of As(V) and other HMs in soil samples were investigated under different conditions. Results demonstrated that M-EMS had a maximum As(V) adsorption capacity of 65.3 mg/g in the aquatic samples. Adding M-EMS to the soil reduced the leaching of As (from 657.2 to 319.8 µg/L) and other HMs after 30 d of incubation, reduced the bioavailability of As(V) and improved the quality and microbial activity of the soil. The mechanism for M-EMS to immobilize As in the soil are complex reactions, ion exchange reaction with As and electrostatic adsorption. This work provides new ideas of using waste residue matrix composites for sustainable remediation of Arsenic in the aquatic environment and soil.

Enhancing degradation of organic matter in microbial electrolytic cells coupled with anaerobic digestion (MEC-AD) systems by carbon-based materials.

Currently, little information is available on relative contributions among biochar (BC), activated carbon (AC), magnetic BC (MBC), and magnetic AC (MAC) to enhance the effectiveness of a microbial electrolytic cells coupled with anaerobic digestion (MEC-AD) system and the impact of carbon-based materials on microbial community. In this study, six anaerobic reactors were constructed to demonstrate the effects of different carbon-based materials on organic matter elimination in the MEC-AD system. Remarkably, the reactor containing MBC exhibited a significant increase in organic removal, achieving 95.0 % chemical oxygen demand (COD) eradication. Additionally, the MBC-added MEC-AD reactor yields acetic acid at a rate 2.9 times higher than that of the BC-added reactor. Electrical stimulation enriched electro-producing bacteria such as Pseudomonas (18.1 %) and Gordonia (6.8 %), which were further promoted by the addition of MBC, indicating that the microbial communities cultivated with the MBC could provide the necessary microbiome for the MEC.

Efficient photo-adsorptive eradication of endocrine disrupting pesticides by chitosan co- decorated metal oxide bio-nanocomposite.

Extensive consumption, toxicity and bioaccumulation of malathion (MLT) and lindane (γ-HCH) pesticides collectively attract the world's attention. Herein, the nanocomposite of chitosan wrapped NiO@ZnO was synthesized by a green methodology using Azadirachta indica leaves extract. Structural and morphological analysis of chitosan-NiO@ZnO showed hollow sphere-flake shaped image adsorbed on a solid chitosan surface with a large surface area of 73 m2g-1. A decrease in values of lattice strain, dislocation density and crystallite size described the imperfection in crystal geometry and new peaks in FT-IR spectra at 698 cm-1 and 448 cm-1 of Ni-N and Zn-N, which respectively confirm the coupling. Chitosan-NiO@ZnO and individual nanoparticles (NiO and ZnO) were well-characterized and utilized for degradation MLT and γ-HCH under direct sunlight and dark conditions. The highest degradation of pesticides (above 94%) resulted with 2 mg L-1 and 10 mg L-1 of MLT (π-π) and γ-HCH, respectively with a 20 mg catalyst dose, and pH of ~ 7 under daylight exposure (5 h). Chitosan-NiO@ZnO substantially suppressed the half-life of the targeted pesticides (MLT: 0.48 h; HCH 0.51 h) and demonstrated the first-order kinetics with a high adsorption capacity, Xm (MLT: 14.5 mg g-1 and γ-HCH 20.7 mg g-1), which also confirmed the strong binding with the pesticides, followed by their conversion into safer and smaller metabolites. The charge separation mechanism was elucidated by UV reflectance and photoluminescence data. Hydroxyl radicals were most frequently responsible for the degradation of pesticides as confirmed by scavenger analysis. The synthesized green-nano photocatalyst showed high reusability (up to 10th cycles), sensitivity and stability within the degradation process, presumably making it suitable for industrial applications.

A biomimetic beetle-like membrane with superoleophilic SiO2-induced oil coalescence on superhydrophilic CuC2O4 nanosheet arrays for effective O/W emulsion separation.

It is highly attractive to develop highly efficient oil-in-water (O/W) emulsion separation technologies for promoting the oily wastewater treatment. Herein, a novel inversely Stenocara beetle-like hierarchical structure of superhydrophobic SiO2 nanoparticle-decorated CuC2O4 nanosheet arrays were prepared on copper mesh membrane by bridging polydopamine (PDA) to make a SiO2/PDA@CuC2O4 membrane for substantially enhanced separation of O/W emulsions. The superhydrophobic SiO2 particles on the as-prepared SiO2/PDA@CuC2O4 membranes were served as localized active sites to induce coalescence of small-size oil droplets in oil-in-water (O/W) emulsions. Such innovated membrane delivered outstanding demulsification ability of O/W emulsion with a high separation flux of 2.5 kL⋅m-2⋅h-1 and its filtrate's chemical oxygen demand (COD) being 30 and 100 mg⋅L-1 for surfactant-free emulsion (SFE) and surfactant-stabilized emulsion (SSE), respectively, and also exhibited a good anti-fouling performance in cycling tests. The innovative design strategy developed in this work broadens the application of superwetting materials for oil-water separation and presents a promising prospect in practical oily wastewater treatment applications.

Preparation of phosphogypsum-copper smelting slag-based consolidating body with high compressive strength.

Phosphogypsum (PG) is an industrial waste residue produced during the production of phosphoric acid through the wet process. With strong acidity and a large amount of toxic impurities, PG is difficult to reuse. In this study, the solidified body (PG-S) was made by mechanical compression of the mixture of PG, copper smelting slag (CSS), CaO, NaOH, and water. Results indicate that the composition of the material phases in the PG-S samples changed with hydrated calcium silicate and amorphous silicate derivatives were formed during the reaction; Fe and Ca in the material were transformed; and the prepared geopolymer material had a dense internal structure with the materials being cemented to each other. The highest compressive strength of PG-S cured for 28 days could reach 21.3 MPa with a fixation efficiency of PO43-and F-reaching 99.81 and 94.10%, respectively. The leaching concentration of heavy metals of the PG-S cured for 28 days met the requirements of the Comprehensive Wastewater Discharge Standard (GB 8978-1996). The simulation results of the geochemical model verified the feasibility of the whole immobilization process from the thermodynamic point of view. This work directly uses copper smelting slag and phosphogypsum for coupled immobilization/stabilization treatment not only to achieve the immobilization of pollutants in both solid wastes but also to obtain colloidal masses with certain compressive strength, which also provides a new option for resource utilization of phosphogypsum and copper smelting slag. This work also shows great potential in turning the actual mine backfill into cementitious material.

Using innovative copper-loaded activated alumina (Cu/AA) as the catalyst for catalytic wet peroxidation (CWPO) of catechol.

In this study, copper-loaded activated alumina (Cu/AA) was synthesized and used for the CWPO of catechol (a representative refractory organic pollutant). Various characterization techniques were deployed to characterize the catalysts, e.g., activated alumina (AA), as well as pristine and spent 1% Cu/AA. The innovative 1% Cu/AA catalyst exhibited good thermal stability up to 1173 K with a marginal weight loss of 13%. The Cu species were well dispersed on the activated alumina framework with no significant cluster formation. Typically, the average copper particle size of 5 nm was dispersed on the AA framework. Catechol removal was observed to be 92% with 87% mineralization at optimized conditions (initial catechol concentration = 200 mg/L, catalyst dose of 1% Cu/AA = 2 g/L; temperature = 323 K; pH = 6; and H2O2/catechol stoichiometric ratio = 0.5). The mineralization of catechol was analyzed using mass spectroscopy, with the associated mechanism has been elucidated. Results of this study indicated that synthesized catalyst has phenomenal advantages in terms of simple separation and high removal efficiency of catechol, suggesting the feasibility of employing Cu/AA as the effective catalyst for the CWPO of catechol.

The microbial synergy and response mechanisms of hydrolysis-acidification combined microbial electrolysis cell system with stainless-steel cathode for textile-dyeing wastewater treatment.

Microbial electrolysis cell (MEC) has been existing problems such as poor applicability to real wastewater and lack of cost-effective electrode materials in the practical application of refractory wastewater. A hydrolysis-acidification combined MEC system (HAR-MECs) with four inexpensive stainless-steel and conventional carbon cloth cathodes for the treatment of real textile-dyeing wastewater, which was fully evaluated the technical feasibility in terms of parameter optimization, spectral analysis, succession and cooperative/competition effect of microbial. Results showed that the optimum performance was achieved with a 12 h hydraulic retention time (HRT) and an applied voltage of 0.7 V in the HAR-MEC system with a 100 µm aperture stainless-steel mesh cathode (SSM-100 µm), and the associated optimum BOD5/COD improvement efficiency (74.75 ± 4.32 %) and current density (5.94 ± 0.03 A·m-2) were increased by 30.36 % and 22.36 % compared to a conventional carbon cloth cathode. The optimal system had effective removal of refractory organics and produced small molecules by electrical stimulation. The HAR segment could greatly alleviate the imbalance between electron donors and electron acceptors in the real refractory wastewater and reduce the treatment difficulty of the MEC segment, while the MEC system improved wastewater biodegradability, amplified the positive and specific interactions between degraders, fermenters and electroactive bacteria due to the substrate complexity. The SSM-100 µm-based system constructed by phylogenetic molecular ecological network (pMEN) exhibited moderate complexity and significantly strong positive correlation between electroactive bacteria and fermenters. It is highly feasible to use HAR-MEC with inexpensive stainless-steel cathode for textile-dyeing wastewater treatment.

A feasibility investigation of a pilot-scale bioelectrochemical coupled anaerobic digestion system with centric electrode module for real membrane manufacturing wastewater treatment.

The large-scale application of bioelectrochemical coupled anaerobic digestion (BES-AD) is limited by the matching of electrode configuration and the applicability of real wastewater. In this study, a pilot-scale BES-AD system with an effective system volume of 5 m3 and a 1 m3 volume of a carbon fiber brush electrode module was constructed and tested for treatment of the membrane manufacturing wastewater. The results showed that the BOD5/COD of the wastewater was increased from 0.238 to 0.398 when the applied voltage was 0.9 V. The pollutants such as N, N-Dimethylacetamide and glycerol in wastewater were degraded significantly. The microorganisms in the electrode modules were spatially enriched. The fermenters (Norank_f__ML635J-40_aquatic_group, 6.55 %; unclassified_f__Propionibacteriaceae, 5.25 %) and degraders (Corynebacterium, 29.31 %) were mostly enriched at the bottom, while electroactive bacteria (Pseudomonas, 29.39 %, Geobacter, 7.86 %) were mostly enriched at the top. Combined with the economical construction and operation cost ($1708.8/m3 and $0.76/m3) of the BES-AD system.

Comparison of GHG emissions from open field burning and anaerobic digestion of rice straw.

Rice straw (RS) has been burned in open fields in many countries, which is a growing environmental concern. Anaerobic digestion (AD) of RS is one of the sustainable alternatives to open burning of RS for converting the biomass into methane, carbon dioxide, and digestate for use as agricultural manure. The present study evaluates the RS generation, use patterns, and greenhouse gas emissions from open field burning and the AD of RS. Results indicate the AD of RS offers greater environmental benefits than that by RS open field burning. As a result of the open burning of RS in India emitted 592032.52 kg of CO2 equivalents/kg per year, whereas AD of RS contributes 122.86 kg of CO2 equivalents/kg per year. If RS were burned in an open field, its Global Warming Potential would be 493,873 times greater than that of AD. By minimizing GHG emissions and creating sustainable energy from waste, sustainable development, and circular economies are achieved.

Toxicity determination, pollution source delineation, and microbial diversity evaluation of PAHs-contaminated sediments for an urban river.

The Feng-Sang River is a metropolitan river in Kaohsiung City, Taiwan. In this study, Feng-Sang River sediments were analyzed to investigate the distributions and sources of polycyclic aromatic hydrocarbons (PAHs). The Sediment Quality Guidelines (SQGs), potentially carcinogenic PAHs (TEQcarc ), and toxic equivalence quotient (TEQ) were applied to evaluate influences of PAHs on ecosystems and microbial diversities. Results indicate that PAHs concentrations varied between seasons and locations. The concentrations of ∑16 PAHs ranged from 73.6 to 603.8 ng/kg in dry seasons and from 2.3 to 199.3 ng/kg in wet seasons. This could be because of the flushing effect during wet seasons, which caused the movement and dilution of the PAH-contaminated sediments. Diagnostic ratio analysis infers that high PAHs levels were generated by combustion processes and vehicle traffic, and results from multivariate descriptive statistical analysis also demonstrate that the vehicular traffic pollution could be the major emission source of PAHs contamination. Comparisons of PAHs with SQGs indicate that PAHs concentrations in sediment were below the effects range low (ERL) values, and thus, the immediate threat to organisms might not be significant. The diagnostic ratio analyses are effective methods for PAH source appointment. The metagenomic assay results imply that sediments contained essential microbial species with eminent diversity. The detected PAH-degrading bacteria (Desulfatiglans, Dechloromonas, Sphingomonas, Methylobacterium, Rhodobacter, Clostridium, and Exiguobacterium) played a key role in PAHs biotransformation, and Dechloromonas and Rhodobacter had a higher relative abundance. Results of microbial diversity analyses indicate that the contaminated environment induced the changes of governing microbial groups in sediments. PRACTITIONER POINTS: Diagnostic ratio analyses are effective methods for PAHs source appointment. Microbial composition in sediments are highly affected by anthropogenic pollution. Combustion and vehicle traffic contribute to urban river sediments pollution by PAHs. Dechloromonas and Rhodobacter are dominant PAHs-degrading bacteria in sediments.