The role of lipids in fermentative propionate production from the co-fermentation of lipid and food waste

● Lipid can promote PA production on a target from food waste. ● PA productivity reached 6.23 g/(L∙d) from co-fermentation of lipid and food waste. ● Lipid promoted the hydrolysis and utilization of protein in food waste. ● Prevotella , Veillonella and norank _f _Propioni bacteriaceae were enriched. ● Main pathway of PA production was the succinate pathway. Food waste (FW) is a promising renewable low-cost biomass substrate for enhancing the economic feasibility of fermentative propionate production. Although lipids, a common component of food waste, can be used as a carbon source to enhance the production of volatile fatty acids (VFAs) during co-fermentation, few studies have evaluated the potential for directional propionate production from the co-fermentation of lipids and FW. In this study, co-fermentation experiments were conducted using different combinations of lipids and FW for VFA production. The contributions of lipids and FW to propionate production, hydrolysis of substrates, and microbial composition during co-fermentation were evaluated. The results revealed that lipids shifted the fermentation type of FW from butyric to propionic acid fermentation. Based on the estimated propionate production kinetic parameters, the maximum propionate productivity increased significantly with an increase in lipid content, reaching 6.23 g propionate/(L∙d) at a lipid content of 50%. Propionate-producing bacteria Prevotella, Veillonella, and norank_f_Propionibacteriaceae were enriched in the presence of lipids, and the succinate pathway was identified as a prominent fermentation route for propionate production. Moreover, the Kyoto Encyclopedia of Genes and Genomes functional annotation revealed that the expression of functional genes associated with amino acid metabolism was enhanced by the presence of lipids. Collectively, these findings will contribute to gaining a better understanding of targeted propionate production from FW.     

Differences in distributions,assembly mechanisms,and putative interactions of AOB and NOB at a large spatial scale

● Nitrifiers in WWTP were investigated at large spatial scale. ● AOB populations varied greatly but NOB populations were similar among cities. ● Drift dominated both AOB and NOB assembling processes. ● DO did not show a significant effect on NOB. ● NOB tended to cooperate with AOB and non-nitrifying microorganisms. Ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB) play crucial roles in removing nitrogen from sewage in wastewater treatment plants (WWTPs) to protect water resources. However, the differences in ecological properties and putative interactions of AOB and NOB in WWTPs at a large spatial scale remain unclear. Hence, 132 activated sludge (AS) samples collected from 11 cities across China were studied by utilizing 16S rRNA gene sequencing technology. Results indicated that Nitrosomonas and Nitrosospira accounted for similar ratios of the AOB community and might play nearly equal roles in ammonia oxidation in AS. However, Nitrospira greatly outnumbered other NOB genera, with proportions varying from 94.7% to 99.9% of the NOB community in all WWTPs. Similar compositions and, hence, a low distance–decay turnover rate of NOB (0.035) across China were observed. This scenario might have partly resulted from the high proportions of homogenizing dispersal (~13%). Additionally, drift presented dominant roles in AOB and NOB assembling mechanisms (85.2% and 81.6% for AOB and NOB, respectively). The partial Mantel test illustrated that sludge retention time and temperature were the primary environmental factors affecting AOB and NOB communities. Network results showed that NOB played a leading role in maintaining module structures and node connections in AS. Moreover, most links between NOB and other microorganisms were positive, indicating that NOB were involved in complex symbioses with bacteria in AS.     

The impact of different voltage application modes on biodegradation of chloramphenicol and shift of microbial community structure

● Presented coupled system enhanced biodegradation of antibiotic chloramphenicol. ● HRT and electrical stimulation modes were key influencing factors. ● Electrical stimulation had little effect on the chloramphenicol metabolic pathway. ● Microbial community structure varied with the voltage application mode. Exoelectrogenic biofilms have received considerable attention for their ability to enhance electron transfer between contaminants and electrodes in bioelectrochemical systems. In this study, we constructed anaerobic-aerobic-coupled upflow bioelectrochemical reactors (AO-UBERs) with different voltage application modes, voltages and hydraulic retention times (HRTs). In addition, we evaluated their capacity to remove chloramphenicol (CAP). AO-UBER can effectively mineralize CAP and its metabolites through electrical stimulation when an appropriate voltage is applied. The CAP removal efficiencies were ~81.1%±6.1% (intermittent voltage application mode) and 75.2%±4.6% (continuous voltage application mode) under 0.5 V supply voltage, which were ~21.5% and 15.6% greater than those in the control system without voltage applied, respectively. The removal efficiency is mainly attributed to the anaerobic chamber. High-throughput sequencing combined with catabolic pathway analysis indicated that electrical stimulation selectively enriched Megasphaera, Janthinobacterium, Pseudomonas, Emticicia, Zoogloea, Cloacibacterium and Cetobacterium, which are capable of denitrification, dechlorination and benzene ring cleavage, respectively. This study shows that under the intermittent voltage application mode, AO-UBERs are highly promising for treating antibiotic-contaminated wastewater.     

Cultivars and oil extraction techniques affect Cd/Pb contents and health risks in oil of rapeseed grown on Cd/Pb-contaminated farmland

● Organic solvent extracted fewer Cd/Pb in rapeseed oil than physical pressing. ● Brassica rapa transferred fewer Cd and Pb from seed to oil than Brassica napus . ● Carcinogenic risk mainly from Cd and worth more concern than noncarcinogenic risk. ● Organic solvent specially SLB pose less heath risk for oil than physical pressing. ● Rapeseed oil posed higher carcinogenic risk for rural residents than urban. Substitute planting with rapeseed offers promise for safely using large areas of Cd/Pb-contaminated farmland. Cd/Pb distributions during rapeseed oil production were investigated and health risks posed by the oil were assessed. Tests were performed using three cultivars (Brassica rapa SYH and ZS100 and Brassica napus QY-1) and four oil extraction techniques (mechanical and low-temperature pressing and n-hexane and subcritical low-temperature butane extraction). The amounts of Cd and Pb in oil were 0.73%–8.44% and 3.14%–11.76%, respectively, of the amounts in rapeseed and were strongly affected by the cultivar and oil extraction technique. The heavy metal (HM) concentrations were lower in solvent-extracted oil (particularly subcritical low-temperature butane extracted oil, in which HMs were not detected) than mechanically pressed oil. The Cd and Pb transfer indices were lower (meaning larger proportions of HMs were retained by the rapeseed meal) for B. rapa than B. napus. This was attributed to a high HM binding protein content of B. rapa seed. Health risks to humans were assessed using a probabilistic risk assessment model. The carcinogenic risk was mainly (97.1%–99.9%) caused by Cd and poses more concern than non-carcinogenic risk. Stronger health risks are posed by mechanically pressed than solvent-extracted oil, and higher carcinogenic risks are posed to people living in rural areas than urban areas. Substitute planting with B. rapa and extracting oil with organic solvent (preferably subcritical low-temperature butane) are optimal for safely utilizing Cd/Pb-contaminated soil. Attention should be paid to the health risks posed by Cd in oil to rural populations.     

Chromium phytoextraction and physiological responses of the hyperaccumulator Leersia hexandra Swartz to plant growth-promoting rhizobacterium inoculation

● Improved Cr phytoextration efficiency was achieved by B. cereus inoculation. ● B. cereus could produce plant-beneficial PGPR factors at diverse Cr stresses. ● Enhanced resistance of inoculated L. hexandra towards elevated Cr stress. ● The majority of Cr existed in the stable forms in the tissues of L. hexandra. Phytoextraction is a promising option for purifying hexavalent chromium (Cr(VI))-laden wastewater, but the long remediation period incurred by poor growth rate of Cr hyperaccumulators remains a primary hindrance to its large-scale application. In this study, we performed a hydroponic experiment to evaluate the feasibility of promoting the growth and phytoextraction efficiency of Cr hyperaccumulator Leersia hexandra Swartz (L. hexandra) by inoculating plant growth-promoting rhizobacteria (PGPR) Bacillus cereus (B. cereus). In batch tests, the Cr(VI) removal rates of L. hexandra and B. cereus co-culture were greater than the sum of their respective monocultures. This was likely due to the microbial reduction of Cr(VI) to Cr(III), which is amiable to plant uptake. Besides, the PGPR factors of B. cereus, including indoleacetic acid (IAA) production, 1-aminocyclopropane-1-carboxylic acid deamination (ACCd) activity, phosphate solubilization capacity, and siderophore production, were quantified. These PGPR factors helped explain the biomass augmentation, root elongation and enhanced Cr enrichment of the inoculated L. hexandra in pot experiments. Despite the increased Cr uptake, no aggravated oxidative damage to the cell membrane was observed in the inoculated L. hexandra. This was attributed to its capacity to confront the increased intracellular Cr stress by upregulating both the activities of antioxidative enzymes and expression of metal-binding proteins/peptides. Moreover, L. hexandra could always conserve the majority of Cr in the residual and oxalic integrated forms with low mobility and phytotoxicity, irrespective of the B. cereus inoculation. These results highlight the constructed Cr hyperaccumulator-rhizobacteria consortia as an effective candidate for decontaminating Cr(VI)-laden wastewater.     

Evaluating the impact of sulfamethoxazole on hydrogen production during dark anaerobic sludge fermentation

● SMX promotes hydrogen production from dark anaerobic sludge fermentation. ● SMX significantly enhances the hydrolysis and acidification processes. ● SMX suppresses the methanogenesis process in order to reduce hydrogen consumption. ● SMX enhances the relative abundance of hydrogen-VFAs producers. ● SMX brings possible environmental risks due to the enrichment of ARGs. The impact of antibiotics on the environmental protection and sludge treatment fields has been widely studied. The recovery of hydrogen from waste activated sludge (WAS) has become an issue of great interest. Nevertheless, few studies have focused on the impact of antibiotics present in WAS on hydrogen production during dark anaerobic fermentation. To explore the mechanisms, sulfamethoxazole (SMX) was chosen as a representative antibiotic to evaluate how SMX influenced hydrogen production during dark anaerobic fermentation of WAS. The results demonstrated SMX promoted hydrogen production. With increasing additions of SMX from 0 to 500 mg/kg TSS, the cumulative hydrogen production elevated from 8.07 ± 0.37 to 11.89 ± 0.19 mL/g VSS. A modified Gompertz model further verified that both the maximum potential of hydrogen production (P_m) and the maximum rate of hydrogen production (R_m) were promoted. SMX did not affected sludge solubilization, but promoted hydrolysis and acidification processes to produce more hydrogen. Moreover, the methanogenesis process was inhibited so that hydrogen consumption was reduced. Microbial community analysis further demonstrated that the introduction of SMX improved the abundance of hydrolysis bacteria and hydrogen-volatile fatty acids (VFAs) producers. SMX synergistically influenced hydrolysis, acidification and acetogenesis to facilitate the hydrogen production.     

Evaluation of 1,4-naphthoquinone derivatives as antibacterial agents: activity and mechanistic studies

● All 1,4-naphthoquinone hybrids exhibited significant antimicrobial activity. ● Presence of a hydroxyl group on aromatic B-ring of juglone was crucial for activity. ● Juglone can cause DNA damage by producing ROS and downregulation of RecA. ● Juglone has the potential to become a disinfectant. The diverse and large-scale application of disinfectants posed potential health risks and caused ecological damage during the 2019-nCoV pandemic, thereby increasing the demands for the development of disinfectants based on natural products, with low health risks and low aquatic toxicity. In the present study, a few natural naphthoquinones and their derivatives bearing the 1,4-naphthoquinone skeleton were synthesized, and their antibacterial activity against selected bacterial strains was evaluated. In vitro antibacterial activities of the compounds were investigated against Escherichia coli and Staphylococcus aureus. Under the minimum inhibitory concentration (MIC) of ≤ 0.125 μmol/L for juglone (1a), 5,8-dimethoxy-1,4-naphthoquinone (1f), and 7-methyl-5-acetoxy-1,4-naphthoquinone (3c), a strong antibacterial activity against S. aureus was observed. All 1,4-naphthoquinone derivatives exhibited a strong antibacterial activity, with MIC values ranging between 15.625 and 500 μmol/L and EC₅₀ values ranging between 10.56 and 248.42 μmol/L. Most of the synthesized compounds exhibited strong antibacterial activities against S. aureus. Among these compounds, juglone (1a) showed the strongest antibacterial activity. The results from mechanistic investigations indicated that juglone, a natural naphthoquinone, caused cell death by inducing reactive oxygen species production in bacterial cells, leading to DNA damage. In addition, juglone could reduce the self-repair ability of bacterial DNA by inhibiting RecA expression. In addition to having a potent antibacterial activity, juglone exhibited low cytotoxicity in cell-based investigations. In conclusion, juglone is a strong antibacterial agent with low toxicity, indicating that its application as a bactericidal agent may be associated with low health risks and aquatic toxicity.     

Ozonation of aromatic monomer compounds in water: factors determining reaction outcomes

● p- CNB and IBP were selected, to explore factors determining ozonation outcomes. ● •OH contributed only 50 % to IBP removal, compared to the 90 % for p -CNB removal. ● IBP achieved fewer TOC removal and more by-product types and quantities. ● A longer ring-opening distance existed during the degradation of IBP. ● Multiple positions on both branches of IBP were attacked, consuming more oxidants. For aromatic monomer compounds (AMCs), ozonation outcomes were usually predicted by the substituents of the benzene ring based on the electron inductive effect. However, the predicted results were occasionally unreliable for complex substituents, and other factors caused concern. In this study, p-chloronitrobenzene (p-CNB) and ibuprofen (IBP) were selected for ozonation. According to the electron inductive theory, p-CNB should be less oxidizable, but the opposite was true. The higher rates of p-CNB were due to various sources of assistance. First, the hydroxyl radical (•OH) contributed 90 % to p-CNB removal at pH 7.0, while its contribution to IBP removal was 50 %. Other contributions came from molecular O₃ oxidation. Second, p-CNB achieved 40 % of the total organic carbon (TOC) removal and fewer by-product types and quantities, when compared to the results for IBP. Third, the oxidation of p-CNB started with hydroxyl substitution reactions on the benzene ring; then, the ring opened. However, IBP was initially oxidized mainly on the butane branched chain, with a chain-shortening process occurring before the ring opened. Finally, the degradation pathway of p-CNB was single and consumed fewer oxidants. However, both branches of IBP were attacked simultaneously, and three degradation pathways that relied on more oxidants were proposed. All of these factors were determinants of the rapid removal of p-CNB.     

Effect of loading rate on shear strength parameters of mechanically and biologically treated waste

● Mechanical behavior of MBT waste affected by loading rate was investigated. ● Shear strength ratio of MBT waste increases with an increase in loading rate. ● Cohesion is inversely related to loading rate. ● Internal friction angles are positively related to loading rate. ● MBT waste from China shows smaller range of φ. Mechanical biological treatment (MBT) technology has attracted increasing attention because it can reduce the volume of waste produced. To deal with the current trend of increasing waste, MBT practices are being adopted to address waste generated in developing urban societies. In this study, a total of 20 specimens of consolidated undrained triaxial tests were conducted on waste obtained from the Hangzhou Tianziling landfill, China, to evaluate the effect of loading rate on the shear strength parameters of MBT waste. The MBT waste samples exhibited an evident strain-hardening behavior, and no peak was observed even when the axial strain exceeded 25%. Further, the shear strength increased with an increase in the loading rate; the effect of loading rate on shear strength under a low confining pressure was greater than that under a high confining pressure. Furthermore, the shear strength parameters of MBT waste were related to the loading rate. The relationship between the cohesion, internal friction angle, and logarithm of the loading rate could be fitted to a linear relationship, which was established in this study. Finally, the ranges of shear strength parameters cohesion c and effective cohesion c ´ were determined as 1.0–8.2 kPa and 2.1–14.9 kPa, respectively; the ranges of the internal friction angle φ and effective internal friction angle φ ´ were determined as 16.2°–29° and 19.8°–43.9°, respectively. These results could be used as a valuable reference for conducting stability analyses of MBT landfills.     

Relationship between groundwater cadmium and vicinity resident urine cadmium levels in the non-ferrous metal smelting area,China

● This study systematically examined the relationship between groundwater Cd and UCL. ● The study covered 211 UCL and sociological characteristic from nine groundwater samples. ● We found a significant positive correlation between groundwater Cd and UCL. ● Smoking status and education level also significantly affected UCL. Cadmium (Cd) has received widespread attention owing to its persistent toxicity and non-degradability. Cd in the human body is mainly absorbed from the external environment and is usually assessed using urinary Cd. Hunan Province is the heartland of the Chinese non-ferrous mining area, where several serious Cd pollution events have occurred, including high levels of Cd in the urine of residents. However, the environmental factors influencing high urinary Cd levels (UCLs) in nearby residents remain unclear. Therefore, 211 nearby residents’ UCLs and the corresponding sociological characteristics from nine groundwater samples in this area were analyzed using statistical analysis models. Groundwater Cd concentration ranged from 0.02 to 1.15 μg/L, aligning with class III of the national standard; the range of UCL of nearby residents was 0.37–36.60 μg/L, exceeding the national guideline of 0–2.5 μg/L. Groundwater Cd levels were positively correlated with the UCL (P < 0.001, correlation coefficient 95 % CI = 9.68, R² = 0.06). In addition, sociological characteristics, such as smoking status and education level, also affect UCL. All results indicate that local governments should strengthen the prevention and abatement of groundwater Cd pollution. This study is the first to systematically evaluate the relationship between groundwater Cd and UCL using internal and external environmental exposure data. These findings provide essential bases for relevant departments to reduce Cd exposure in regions where the heavy metal industry is globally prevalent.     

Insights into the changes of amino acids,microbial community,and enzymatic activities related with the nutrient quality of product during the composting of food waste

● The highest seed germination index was achieved at 0.3 g/g total solids of food waste. ● Proline was identified as the key amino acid related with the composting process. ● Amino acid metabolism sequences predominated during the whole composting process. This study systematically investigated the changes of amino acids as the composting process of food waste proceeded. It is found that the addition of 0.3 g/g total solids of food waste achieved the highest seed germination index of the product (268 %). The microbial community results indicated that the abundance of amino acid metabolism sequences remained at high levels during the whole composting process. Proline was identified as the key amino acid related with the nutrient quality of product during the composting of food waste. Further plant germination and hydroponic experiments found, that compared with those without the addition of proline, the addition of 50 mg/L proline increased seed germination rate by 20 %, increased shoot length by 3 %, increased root biomass of seedlings by 82 %, and increased leaf biomass of seedlings by 76 %, respectively. Firmicutes, γ-Pseudomonadota, Chloroflexi and Planctomycetes were the key identified bacteria related with the increase of proline during the composting of food waste. Meanwhile, the enzymatic tests of the activities of superoxide dismutase, peroxidase and malondialdehyde indicated that proline did not cause oxidative damage on the growth of plants. This study provided novel insights into the changes of amino acids, microbial community, and enzymatic activities related with the nutrient quality of product during the composting of food waste.     

Responses of microbial interactions to elevated salinity in activated sludge microbial community

● Salinity led to the elevation of NAR over 99.72%. ● Elevated salinity resulted in a small, complex, and more competitive network. ● Various AOB or denitrifiers responded differently to elevated salinity. ● Putative keystone taxa were dynamic and less abundant among various networks. Biological treatment processes are critical for sewage purification, wherein microbial interactions are tightly associated with treatment performance. Previous studies have focused on assessing how environmental factors (such as salinity) affect the diversity and composition of the microbial community but ignore the connections among microorganisms. Here, we described the microbial interactions in response to elevated salinity in an activated sludge system by performing an association network analysis. It was found that higher salinity resulted in low microbial diversity, and small, complex, more competitive overall networks, leading to poor performance of the treatment process. Subnetworks of major phyla (Proteobacteria, Bacteroidetes, and Chloroflexi) and functional bacteria (such as AOB, NOB and denitrifiers) differed substantially under elevated salinity process. Compared with subnetworks of Nitrosomonadaceae, Nitrosomonas (AOB) made a greater contribution to nitrification under higher salinity (especially 3%) in the activated sludge system. Denitrifiers established more proportion of cooperative relationships with other bacteria to resist 3% salinity stress. Furthermore, identified keystone species playing crucial roles in maintaining process stability were dynamics and less abundant under salinity disturbance. Knowledge gleaned from this study deepened our understanding of microbial interaction in response to elevated salinity in activated sludge systems.     

Highly efficient and selective removal of phosphate from wastewater of sea cucumber aquaculture for microalgae culture using a new adsorption-membrane separation-coordinated strategy

● A new adsorption-membrane separation strategy is used for phosphate removal. ● PVC/Zr-BT shows a selective adsorption ability to low-concentration phosphate. ● Low concentration of P below 0.05 mg/L was achieved in actual wastewater treatment. ● Algal biomass production served as a demonstration of phosphorus recycling. Enhanced phosphorus treatment and recovery has been continuously pursued due to the stringent wastewater discharge regulations and a phosphate supply shortage. Here, a new adsorption-membrane separation strategy was developed for rational reutilization of phosphate from sea cucumber aquaculture wastewater using a Zr-modified-bentonite filled polyvinyl chloride membrane. The as-obtained polyvinyl chloride/Zr-modified-bentonite membrane was highly permeability (940 L/(m²·h)), 1–2 times higher than those reported in other studies, and its adsorption capacity was high (20.6 mg/g) when the phosphate concentration in water was low (5 mg/L). It remained stable under various conditions, such as different pH, initial phosphate concentrations, and the presence of different ions after 24 h of adsorption in a cross-flow filtration system. The total phosphorus and phosphate removal rate reached 91.5% and 95.9%, respectively, after the membrane was used to treat sea cucumber aquaculture wastewater for 24 h and no other water quality parameters had been changed. After the purification process, the utilization of the membrane as a new source of phosphorus in the phosphorus-free f/2 medium experiments indicated the high cultivability of economic microalgae Phaeodactylum tricornutum FACHB-863 and 1.2 times more chlorophyll a was present than in f/2 medium. The biomass and lipid content of the microalgae in the two different media were similar. The innovative polyvinyl chloride/Zr-modified-bentonite membrane used for phosphorus removal and recovery is an important instrument to establish the groundwork for both the treatment of low concentration phosphate from wastewater as well as the reuse of enriched phosphorus in required fields.     

Hybrid energy harvesting systems for self-powered sustainable water purification by harnessing ambient energy

● Energy harvesters harness multiple energies for self-powered water purification. ● Hybrid energy harvesters enable continuous output under fluctuating conditions. ● Mechanical, thermal, and solar energies enable synergic harvesting. ● Perspectives of hybrid energy harvester-driven water treatment are proposed. The development of self-powered water purification technologies for decentralized applications is crucial for ensuring the provision of drinking water in resource-limited regions. The elimination of the dependence on external energy inputs and the attainment of self-powered status significantly expands the applicability of the treatment system in real-world scenarios. Hybrid energy harvesters, which convert multiple ambient energies simultaneously, show the potential to drive self-powered water purification facilities under fluctuating actual conditions. Here, we propose recent advancements in hybrid energy systems that simultaneously harvest various ambient energies (e.g., photo irradiation, flow kinetic, thermal, and vibration) to drive water purification processes. The mechanisms of various energy harvesters and point-of-use water purification treatments are first outlined. Then we summarize the hybrid energy harvesters that can drive water purification treatment. These hybrid energy harvesters are based on the mechanisms of mechanical and photovoltaic, mechanical and thermal, and thermal and photovoltaic effects. This review provides a comprehensive understanding of the potential for advancing beyond the current state-of-the-art of hybrid energy harvester-driven water treatment processes. Future endeavors should focus on improving catalyst efficiency and developing sustainable hybrid energy harvesters to drive self-powered treatments under unstable conditions (e.g., fluctuating temperatures and humidity).     

Removal of ammonium and nitrate through Anammox and FeS-driven autotrophic denitrification

● Simultaneous NH₄⁺/NO₃^– removal was achieved in the FeS denitrification system ● Anammox coupled FeS denitrification was responsible for NH₄⁺/NO₃^– removal ● Sulfammox, Feammox and Anammox occurred for NH₄⁺ removal ● Thiobacillus, Nitrospira , and Ca. Kuenenia were key functional microorganisms An autotrophic denitrifying bioreactor with iron sulfide (FeS) as the electron donor was operated to remove ammonium (NH₄⁺) and nitrate (NO₃⁻) synergistically from wastewater for more than 298 d. The concentration of FeS greatly affected the removal of NH₄⁺/NO₃⁻. Additionally, a low hydraulic retention time worsened the removal efficiency of NH₄⁺/NO₃⁻. When the hydraulic retention time was 12 h, the optimal removal was achieved with NH₄⁺ and NO₃⁻ removal percentages both above 88%, and the corresponding nitrogen removal loading rates of NH₄⁺ and NO₃⁻ were 49.1 and 44.0 mg/(L·d), respectively. The removal of NH₄⁺ mainly occurred in the bottom section of the bioreactor through sulfate/ferric reducing anaerobic ammonium oxidation (Sulfammox/Feammox), nitrification, and anaerobic ammonium oxidation (Anammox) by functional microbes such as Nitrospira, Nitrosomonas, and Candidatus Kuenenia. Meanwhile, NO₃⁻ was mainly removed in the middle and upper sections of the bioreactor through autotrophic denitrification by Ferritrophicum, Thiobacillus, Rhodanobacter, and Pseudomonas, which possessed complete denitrification-related genes with high relative abundances.     

Catalytic reduction of water pollutants: knowledge gaps,lessons learned,and new opportunities

● Advances, challenges, and opportunities for catalytic water pollutant reduction. ● Cases of Pd-based catalysts for nitrate, chlorate, and perchlorate reduction. ● New functionalities developed by screening and design of catalytic metal sites. ● Facile catalyst preparation approaches for convenient catalyst optimization. ● Rational design and non-decorative effort are essential for future work. In this paper, we discuss the previous advances, current challenges, and future opportunities for the research of catalytic reduction of water pollutants. We present five case studies on the development of palladium-based catalysts for nitrate, chlorate, and perchlorate reduction with hydrogen gas under ambient conditions. We emphasize the realization of new functionalities through the screening and design of catalytic metal sites, including (i) platinum group metal (PGM) nanoparticles, (ii) the secondary metals for improving the reaction rate and product selectivity of nitrate reduction, (iii) oxygen-atom-transfer metal oxides for chlorate and perchlorate reduction, and (iv) ligand-enhanced coordination complexes for substantial activity enhancement. We also highlight the facile catalyst preparation approach that brought significant convenience to catalyst optimization. Based on our own studies, we then discuss directions of the catalyst research effort that are not immediately necessary or desirable, including (1) systematic study on the downstream aspects of under-developed catalysts, (2) random integration with hot concepts without a clear rationale, and (3) excessive and decorative experiments. We further address some general concerns regarding using H₂ and PGMs in the catalytic system. Finally, we recommend future catalyst development in both “fundamental” and “applied” aspects. The purpose of this perspective is to remove major misconceptions about reductive catalysis research and bring back significant innovations for both scientific advancements and engineering applications to benefit environmental protection.     

Genome-resolved metagenomic analysis reveals different functional potentials of multiple Candidatus Brocadia species in a full-scale swine wastewater treatment system

● Four Ca. Brocadia species were observed during the spontaneously enrichment. ● Novel anammox species SW510 and SW773 dominated the full-scale ecosystem. ● Urease and cyanase genes were detected in the new anammox genomes. ● Functional differentiation potentially facilitated co-occurrence of anammox species. The increasing application of anammox processes suggests their enormous potential for nitrogen removal in wastewater treatment facilities. However, the functional potentials and ecological differentiation of cooccurring anammox species in complex ecosystems have not been well elucidated. Herein, by utilizing functional reconstruction and comparative genome analysis, we deciphered the cooccurring mechanisms of four Candidatus Brocadia species that were spontaneously enriched in a full-scale swine wastewater treatment system. Phylogenetic analysis indicated that species SW172 and SW745 were closely related to Ca. Brocadia caroliniensis and Ca. Brocadia sapporoensis, respectively, whereas the dominant species SW510 and SW773, with a total average abundance of 34.1%, were classified as novel species of the genus Ca. Brocadia. Functional reconstruction revealed that the novel species SW510 can encode both cytochrome cd₁-type nitrite reductase and hydroxylamine oxidase for nitrite reduction. In contrast, the detected respiratory pentaheme cytochrome c nitrite reductase and acetate kinase genes suggested that SW773 likely reduced nitrite to ammonium with acetate as a carbon source. Intriguingly, the presence of genes encoding urease and cyanase indicated that both novel species can use diverse organic nitrogen compounds in addition to ammonia and nitrite as substrates. Taken together, the recovery and comparative analysis of these anammox genomes expand our understanding of the functional differentiation and cooccurrence of the genus Ca. Brocadia in wastewater treatment systems.     

Perfluoroalkane acids in human milk under the global monitoring plan of the Stockholm Convention on Persistent Organic Pollutants (2008–2019)

● Perfluorooctanesulfonic acid and perfluorooctanoic acid highest in human milk. ● All other perfluoroalkane substances had median values of zero (101 samples). ● Branched PFOS recommended to be analyzed separately from linear isomer. ● PFOS and PFOA showed differentiated regional and income distribution. ● Human health risk assessment values not yet available at global level. Within the global monitoring plan (GMP) established by article 16 of the Stockholm Convention on Persistent Organic Pollutants, perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorohexane sulfonic acid (PFHxS) are recommended for analysis in core matrices to assess occurrence and changes geographically and with time. In 101 samples consisting of 86 national pools and 15 pools from States in Brazil obtained between 2008 and 2019, PFHxS was detected in 17% of the national pools and none in Brazil. PFOA and PFOS had a detection frequency of 100% and 92%, respectively. Other perfluoroalkane substances (PFAS) had either low detection frequencies and median values of zero (carboxylic acids C₄–C₁₁; except PFOA) or could not be quantified in any sample (sulfonic acids, C₄–C₁₀, and long-chain carboxylic acids, C₁₂–C₁₄). Correlation between PFOA and PFOS was moderately (r = 0.58). Whereas median values were almost identical (18.9 pg/g f.w. for PFOS; 18.6 pg/g f.w. for PFOA), PFOS showed larger ranges (< 6.2 pg/g f.w.–212 pg/g f.w.) than PFOA (< 6.2 pg/g f.w.–63.4 pg/g f.w.). It was shown that wealthier countries had higher PFOA concentrations than poorer countries. No difference in concentrations was found for samples collected in countries having or not having ratified the Stockholm Convention amendments to list PFOS or PFOA. The goal to achieve 50% decrease in concentrations within ten years was met by Antigua and Barbuda, Kenya, and Nigeria for PFOS and by Antigua and Barbuda for PFOA. In a few cases, increases were observed; one country for PFOS, four countries for PFOA.     

China’s carbon neutrality: an extensive and profound systemic reform

● China has pledged ambitious carbon peak and neutrality goals for mitigating global climate change. ● Major challenges to achieve carbon neutrality in China are summarized. ● The new opportunities along the pathway of China’s carbon neutrality are discussed from four aspects. ● Five policy suggestions for China are provided. China is the largest developing economy and carbon dioxide emitter in the world, the carbon neutrality goal of which will have a profound influence on the mitigation pathway of global climate change. The transition towards a carbon-neutral society is integrated into the construction of ecological civilization in China, and brings profound implications for China’s socioeconomic development. Here, we not only summarize the major challenges in achieving carbon neutrality in China, but also identify the four potential new opportunities: namely, the acceleration of technology innovations, narrowing regional disparity by reshaping the value of resources, transforming the industrial structure, and co-benefits of pollution and carbon mitigation. Finally, we provide five policy suggestions and highlight the importance of balancing economic growth and carbon mitigation, and the joint efforts among the government, the enterprises, and the residents.     

The distribution and availability of phosphorus fractions in restored cut slopes soil aggregates: a case study of subalpine road,Southwest China

● There was no significant difference in soil aggregates TP along altitude gradient. ● Overall, PAC dropped steadily as aggregate size increased. ● In soil aggregate sizes, TPi > TPo > R-P at 3009,3347 and 3654 m except 3980 m. ● Active NaHCO₃-Pi was the main AP source. ● Proportion of small aggregate sizes was emphasized to increase AP storage. The distribution and availability of phosphorus (P) fractions in restored cut slope soil aggregates, along altitude gradients, were analyzed. Samples were collected at 3009, 3347, 3654 and 3980 m of altitude. We examined soil aggregates total phosphorus (TP), available phosphorus (AP) and phosphorus activation coefficient (PAC), and discovered that there was no significant difference in TP levels between all four altitudes samples (p > 0.05). However, there was a significant difference in AP at 3009, 3347 and 3980 m of altitude (p < 0.05). At the altitudes of 3009, 3347 and 3654 m, the AP accumulation in small size aggregates was more advantageous. Overall, PAC dropped steadily as soil aggregates sizes increased, as shown: PAC (3654 m) > PAC (3347 m) > PAC (3009 m) > PAC (3980 m). In all particle size soil aggregates, the distribution of the P fractions was as follows: total inorganic phosphorus (TPi) > total organic phosphorus (TPo) > residual phosphorus (R-P), at 3009, 3347 and 3654 m, but a different registry was observed at 3980 m of altitude: TPo > TPi > R-P. Through correlation and multiple stepwise regression analysis, it was concluded that active NaHCO₃-Pi was the main AP source. It was also suggested that more attention should be given to the ratio of small particle size aggregates to increase soil AP storage. In order to improve the activation capacity and supply of soil P, along with promotion of the healthy development of soil ecosystem on slope land, it was suggest that inorganic P fertilizer and P activator could be added to soil at both low (3009 m) and high altitudes (3980 m).