Fluoroquinolones(FQs)have the propensity to accumulate in sediments once introduction into aquatic envi-ronments,thereby posing potential threats to benthic organisms,yet the ecotoxicity of sediment-associated FQs rem...Fluoroquinolones(FQs)have the propensity to accumulate in sediments once introduction into aquatic envi-ronments,thereby posing potential threats to benthic organisms,yet the ecotoxicity of sediment-associated FQs remains unclear.In this study,the toxicokinetics and responses of multiple biomarkers in Bellamya aeruginosa,exposed to the three commonly used FQs(norfloxacin,NOR;ciprofloxacin,CIP;levofloxacin,LEVO)at envi-ronmentally relevant concentrations were investigated under sediment exposure scenario.The results revealed that FQs were effectively ingested by B.aeruginosa from sediments,CIP showing the highest bioaccumulation(180.59μg/kg),followed by NOR(74.49μg/kg)and LEVO(36.02μg/kg).CIP exhibiting a highest uptake rate constant(Ks)(4.64 g/(g·day))and the lowest elimination rate constant(K_(e))(0.05 g/(g·day)).The descending order of biological half-life is as follows:CIP(13.62 days),LEVO(8.14 days),and NOR(6.83 days).NOR induced the activity of superoxide dismutase,catalase,and glutathione-S-transferase while CIP and LEVO depressed their activities and increased malondialdehyde content,indicating a more pronounced oxidative damage to B.aerug-inosa caused by CIP and LEVO than NOR.Furthermore,all three FQs were found to induce DNA damage and elevate acetylcholinesterase activity,suggesting distinct genotoxic and neurotoxic effects.Interestingly,despite its low bioaccumulation potential,LEVO exhibited high toxicity towards B.aeruginosa.These findings enhance our understanding of the ecotoxicity of FQs in sediments,providing further evidence of their potential ecological risks.展开更多
The escalating pace of industrialization has significantly intensified water pollution challenges,for instance,the persistent organic pollutants like methyl orange(MO).Conventional remediation techniques,such as adsor...The escalating pace of industrialization has significantly intensified water pollution challenges,for instance,the persistent organic pollutants like methyl orange(MO).Conventional remediation techniques,such as adsorption and biological degradation,are often hampered by low efficiency and the risk of secondary pollution.Photocatalysis emerges as a promising sustainable alternative;however,the benchmark material titanium dioxide(TiO_(2))suffers from its intrinsic limitations,notably its wide bandgap energy(≥3.4 eV)restricting its activity to the region of the ultraviolet light and its rapid recombination of photogenerated charge carriers.To overcome these constraints,this research focused on synthesizing novel TiO_(2)/Sn_(3)O_(4) heterojunction composite photocatalysts via a solvothermal approach.Comprehensive characterization techniques confirmed the successful formation of the composite,which revealed that ultrathin Sn3O4 nanosheets uniformly coated TiO_(2) nanospheres.This unique architecture effectively reduced the overall crystallinity and introduced the beneficial oxygen vacancies.Under visible-light irradiation(λ≥420 nm),the optimized TiO_(2)/Sn3O4 composite exhibited the exceptional photocatalytic performance,which achieved 96%degradation of MO within just 60 minutes.The calculated apparent kinetic rate constant(0.103 min^(-1))was remarkably(5.15 times)higher than that of pristine TiO_(2).ESR experiments identified that hydroxyl radicals(·OH)was the predominant active species driving the degradation.Furthermore,cyclic degradation tests demonstrated its excellent material stability,with the composite retaining 85%of its initial efficiency after four consecutive reuse cycles.This work underscored the synergistic effects within the TiO_(2)/Sn_(3)O_(4) heterojunction,which significantly enhanced the visible-light absorption,charge separation,and photocatalytic activity,which provided the valuable insights for designing efficient,stable catalysts for the advanced environmental remediation applications.展开更多
Anammox bacteria in constructed wetlands(CWs)play pivotal role in sustainable nitrogen transformation,yet existing studies lack comprehensive analysis of environmental gradients and microbial interactions,both key fac...Anammox bacteria in constructed wetlands(CWs)play pivotal role in sustainable nitrogen transformation,yet existing studies lack comprehensive analysis of environmental gradients and microbial interactions,both key factors in anammox bacteria enrichment.This study investigated the mechanisms driving anammox bacteria enrichment in lab-scale simulated CWs treating high-nitrogen wastewater,focusing on bacterial community re-sponses across wetland layers with various strategies,including continuous up-flow influent,nitrogen loading increase,effluent recirculation,intermittent influent,and anammox bacteria inoculation.Results showed that total relative and absolute abundances of anammox bacteria ranged from 0.77%to 12.50%and from 0.13 to 6.46×10^(7) copies/g,respectively.Dissolved oxygen and pH had significant positive correlations with the absolute abundance of anammox bacteria,while organic matter and nitrate negatively impacted their relative abundance.Permutational multivariate analysis of variance indicated that spatial heterogeneity explained more variation in anammox bacteria abundance(43.44%)compared to operational strategies(8.58%).In terms of microbial interactions,60 dominant species exhibited potential correlations with anammox bacteria,comprising 170 interactions(105 positive and 65 negative),which suggested that anammox bacteria generally foster cooperative relationships with dominant bacteria.Notably,significant interspecies interactions were observed between Candidatus Kuenenia(dominant anammox bacteria in CWs)and species within the genera Chitinivibrio-nia and Anaerolineaceae,suggesting that microbial interactions primarily manifest as indirect facilitative effects rather than direct mutualistic relationships.Given that the Normalized Stochasticity Ratio in CWs were<50%,this study inferred that environmental gradients have greater influence on anammox bacteria than microbial interactions.展开更多
Tropospheric ozone(O_(3))is a harmful air pollutant negatively impacting forest health,causing O_(3)-specific visible foliar injury(O_(3)VFI).Ozone monitoring in forests has usually implemented by passive samplers,alt...Tropospheric ozone(O_(3))is a harmful air pollutant negatively impacting forest health,causing O_(3)-specific visible foliar injury(O_(3)VFI).Ozone monitoring in forests has usually implemented by passive samplers,although they cannot detect the diurnal peak when a significant part of stomatal O_(3)uptake occurs.This results into uncertainties for the calculation of stomatal O_(3)uptake.This study compares the stomatal-flux-based POD1(phytotoxic ozone dose above a threshold of 1 nmol m^(-2)s^(-1))for forest trees/shrubs estimated from data collected by either passive samplers or active O_(3)monitors to evaluate O_(3)damage to plants in terms of O_(3)VFI in the Southern Alps.The study was conducted over two years(2018-2019)in a mountainous Alpine area(Valle Stura,Italy).An integrative monitoring station for active O_(3)monitoring,as well as passive O_(3)monitors,were installed in an open field area(OFD).The O_(3)VFI was investigated in woody species in the light exposed sampling Site(LESS—Betula pendula,Fagus sylvatica,Larix decidua,Populus tremula,Salix caprea,Rubus sp.and Vaccinium myrtillus)in late summer according to the international co-operative programme on assessment and monitoring of air pollution effects on forests(ICP Forests)manual.The results confirmed that Fagus sylvatica and Rubus sp.are O_(3)-sensitive species showing relatively high POD1(>20 mmol m-2),while Larix decidua is O_(3)-tolerant.We derived flux-based critical levels(CL)corresponding to the presence of O_(3)VFI(5,25,and 50%of symptomatic plants along the LESS)from flux-effect relationships for forest protection against O_(3)VFI.The results support the hypothesis that passive samplers cannot detect episodic high stomatal O₃fluxes(>1 nmol m^(-2)s^(-1)).According to the active monitoring,the CL for O_(3)VFI occurrence was estimated to be 17.1 mmol m-2 POD1 for 25%presence and 34.3 mmol m-2 POD1 for 50%presence of symptomatic plants,while passive samplers underestimated POD1 values for CL calculations by 17%on average,with underestimation increasing at higher CL thresholds.The findings demonstrate that active monitoring refines CLs towards a proper quantitative assessment of O_(3)impact,particularly in capturing peak flux events that are crucial for evaluating plant damage and emphasizes the importance of active O₃monitoring for reliable forest health assessments.展开更多
Europe is grappling with a colossal textile waste problem.Over 125 million tonnes of raw materials are devoured by the global industry each year,yet a mere fraction-less than 1%-of these fibres originate from recycled...Europe is grappling with a colossal textile waste problem.Over 125 million tonnes of raw materials are devoured by the global industry each year,yet a mere fraction-less than 1%-of these fibres originate from recycled textiles.The majority faces an unsustainable fate in landfills,incinerators,or is exported.A pivotal new report by Systemiq,"The Textile Recycling Breakthrough,"offers both a stark assessment and a strategic roadmap:Europe has the potential to amplify polyester textile recycling nearly tenfold by 2035,but this hinges on immediate,decisive action from policymakers and the industry.展开更多
Located on the Qinghai-Xizang Plateau,the Xizang Autonomous Region boasts exceptional solar energy resources.Today,sunlight is being converted into electricity by a 100 megawatt(MW)photovoltaic power station in Chabal...Located on the Qinghai-Xizang Plateau,the Xizang Autonomous Region boasts exceptional solar energy resources.Today,sunlight is being converted into electricity by a 100 megawatt(MW)photovoltaic power station in Chabala Township,Quxu County,Lhasa.Built by Huadian(Quxu)New Energy Co.,Ltd,the project is at an average altitude of 4,000 meters above sea level.It has become a powerful driver of green development in the region,ushering in a new chapter of harmonious coexistence between humanity and nature.展开更多
As the chemical industry expands,the use of benzene,toluene,and xylene(collectively known as BTX)in industrial production has increased greatly.Meanwhile,the toxic nature and potential health hazards of BTX gases cann...As the chemical industry expands,the use of benzene,toluene,and xylene(collectively known as BTX)in industrial production has increased greatly.Meanwhile,the toxic nature and potential health hazards of BTX gases cannot be ignored due to low-concentration leaks underline the critical need for rapid and real-time monitoring of these gases.Chemiresistive metal oxide semiconductor(MOS)-based gas sensors,which are extensively used for gas detection in both industrial settings and everyday life,emerge as one of the optimal solutions for trace BTX detection.These sensors are highly valued for their high sensitivity and low detection limits.Nevertheless,the improvement of selectivity towards specific BTX gases to achieve efficient and precise detection still remains challenging.This review summarizes the chemiresistive MOS-based gas sensors designed for BTX detection,categorizing them based on the components of sensing materials-basically into three groups:single-component,single heterojunction,and multiple heterojunctions gas sensing materials.Further,the review proposes the future application prospects of chemiresistive MOS-based BTX gas sensors,with specific emphasis on their significance in promoting industrial safety and environmental monitoring.展开更多
Successfully generating reactive oxygen species(ROS)in a targeted and efficient manner for the detoxification of chlorinated organic pollutants(CPs)is a significant and demanding challenge.Herein,we present an in-situ...Successfully generating reactive oxygen species(ROS)in a targeted and efficient manner for the detoxification of chlorinated organic pollutants(CPs)is a significant and demanding challenge.Herein,we present an in-situ photoreduction strategy to fabricate a composite of palladium(Pd)nanoparticles anchored few-layer carbon nitride nanosheets(Pd-CN).This innovative Pd-CN is then leveraged to activate peroxymonosulfate(PMS)in pursuit of our objective.The incorporation of Pd nanoparticles enhances PMS absorption and targets its terminal oxygen,thereby aiding in the cleavage of the O-O bond.This process generates crucial intermediates,including adsorbed hydroxyl radicals(*OH)and adsorbed atomic oxygen(O*),which are essential for the production of ^(1)O_(2).Consequently,the Pd-CN catalyst demonstrates strong preference for ^(1)O_(2) generation during the PMS activation process,successfully degrading over 95%of pollutants such as 4-chlorophenol(4-CP),2,4-dichlorophenol(2,4-DCP),and 2,4,6-trichlorophenol(2,4,6-TCP)within just 20 min.Additionally,the catalyst exhibits total organic carbon(TOC)removal rates ranging from 49.4%to 31.4%,while the rates for de-chlorination fall between 68.6%and 72.7%.A subsequent continuous-flow treatment experiment has confirmed the application potential of this system,demonstrating consistent catalytic activity for up to 8 h.This promising technique presents an efficient strategy for addressing the high toxicity of chlorinated organic pollutants in contaminated water.展开更多
Triclosan(TCS) poses harmful risks to ecosystems and human health owing to its endocrine-disrupting effects.Therefore,developing an efficient and sustainable technology to degrade TCS is urgently needed.Herein,cobalt ...Triclosan(TCS) poses harmful risks to ecosystems and human health owing to its endocrine-disrupting effects.Therefore,developing an efficient and sustainable technology to degrade TCS is urgently needed.Herein,cobalt oxyhydroxide @covalent organic frameworks(CoOOH@COFs) S-scheme heterojunction was synthesized,which combined the visible-light-driven photocatalysis and peroxymonosulfate(PMS) activation to synergistically generate abundant reactive oxygen species(ROSs) for TCS degradation.The degradation efficiency of TCS reached 100 % within 8 min in the Vis-CoOOH@COFs/PMS system,and the reaction rate constant was 0.456 min^(-1),which was nearly 1.90 and 2.85 times that of single Co OOH and COFs,and2.36 times that under dark condition,respectively.The density functional theory(DFT) calculations confirmed the energy band bending of CoOOH@COFs and S-scheme charge transport from COFs to Co OOH.Both experimental and theoretical analyses indicated that Co OOH@COFs in photocatalytic-PMS activation systems synergistically facilitated photo-generated carrier separation,enhanced interfacial electron transfer,accelerated PMS activation,and generated multiple ROSs.In particular,photogenerated electrons(e^(-))accelerated the Co(Ⅲ)/Co(Ⅱ) redox cycle,while the PMS captured the e-,which significantly decreased the charge combination of Co OOH@COFs.Radicals(O_(2)^(·-),^(·)OH,and SO_(4)^(·-)) and non-radicals(such as ^(1)O_(2),h^(+),and e^(-)) were both presented in the Vis-CoOOH@COFs/PMS system,with O_(2)^(-) playing a dominant role in TCS degradation.Furthermore,the pathway of TCS degradation and toxicity of intermediates were explored by DFT calculation and transformation product identification.Importantly,the environmentally friendly CoOOH@COFs S-scheme heterojunction exhibited excellent stability and reusability.In conclusion,this study innovatively designed an S-scheme heterojunction in the photocatalytic-PMS activation system,providing guidance and theoretical support for efficient and eco-friendly wastewater treatment.展开更多
Oxidative potential(OP)can be used as an indicator of the health risks of particulate matter in the air.To study the variation and sources of OP,we conducted an observation of PM_(2.5) in a megacity in southern China ...Oxidative potential(OP)can be used as an indicator of the health risks of particulate matter in the air.To study the variation and sources of OP,we conducted an observation of PM_(2.5) in a megacity in southern China in winter and spring of 2021.The results show that the average concentration of PM_(2.5) decreased by 47%from winter to spring,while volume-normalized and mass-normalized OP(i.e.,OP_(v) and OP_(m))increased by 6%and 69%,respectively.It suggests that the decline of PM_(2.5) may not necessarily decrease the health risks and the intrinsic toxicity of PM_(2.5).Variations of OP_(v) and OP_(m) among different periods were related to the different source contributions and environmental conditions.The positive matrix factorization model was used to identify the major sources of OP_(v).OP_(v) was mainly contributed by biomass burning/industrial emissions(29%),soil/road dust(20%),secondary sulfate(14%),and coal combustion(13%)in winter.Different major sources were resolved to be secondary sulfate(36%),biological sources(21%),and marine vessels(20%)in spring,presenting the substantial contribution of biological sources.The analysis shows strong associations between OP_(v) and both live and dead bacteria,further confirming the important contribution of bioaerosols to the enhancement of OP.This study highlights the importance of understanding OP in ambient PM_(2.5) in terms of public health impact and provides a new insight into the biological contribution to OP.展开更多
The widespread use of herbicides such as glyphosate isopropyl amine salt(GIS)and atrazine(ATZ)poses significant risks to aquatic ecosystems.This study investigated the single and joint acute toxicity of a 1:1 GIS-ATZ ...The widespread use of herbicides such as glyphosate isopropyl amine salt(GIS)and atrazine(ATZ)poses significant risks to aquatic ecosystems.This study investigated the single and joint acute toxicity of a 1:1 GIS-ATZ mixture on zebrafish(Danio rerio).Acute tests determined 96-h LC_(50) values of 123.41 mg/L for GIS and 103.95 mg/L for ATZ.In the joint toxicity test,these values decreased to 60.96 and 50.88 mg/L,respectively.The Additive Index(AI)analysis revealed a consistent synergistic interaction between the herbicides at all exposure intervals.These findings underscore the enhanced ecological threat of herbicide mixtures and highlight the necessity of considering joint effects in environmental risk assessments.展开更多
Biochar, known as “black gold”, has garnered wide attention in various applications. However, the potential release of toxic organic compounds has raised environmental concerns, thereby limiting its safe and sustain...Biochar, known as “black gold”, has garnered wide attention in various applications. However, the potential release of toxic organic compounds has raised environmental concerns, thereby limiting its safe and sustainable application. Herein, we propose a distillation strategy to simultaneously detoxify biochar and enhance its redox functionality. Multi-factor correlation analysis identified 30 min as the optimal distillation time, which significantly increased the biochar's Brunauer-Emmett-Teller(BET) surface area(by 143%), improved hydrophilicity(with contact angle decreased by 3.8%), and effectively reduced the dissolved organic carbon(DOC) content of the biochar. Regarding the effect of distillation solvent, both water and acetic acid significantly enhanced the electron exchange capacity(EEC) of the biochar, with lactic acid exhibiting the best performance in improving the electron donating capacity(EDC). Meanwhile, distillation with acetic acid achieved optimal detoxification by effectively removing toxic organic compounds such as naphthalene, amines, and aromatic hydrocarbons. Further validation confirmed the good generalizability of this method to biochars derived from various feedstocks. Techno-economic analysis showed a 98.7% reduction in water consumption and 22.9%-62.5% cost savings compared to traditional washing methods. This work highlights distillation as an efficient, eco-friendly, and cost-effective method to enhance biochar safety and redox functionality, thereby advancing its sustainable applications.展开更多
基金supported by the Hunan Provincial Natural Science Foundation of China(Nos.2023JJ40518 and 2023JJ30490)the Scientific Research Foundation of Hunan Provincial Education Department(Nos.21B0511 and 22A0384)the Research Funding Project of Jishou University for talent introduction.
文摘Fluoroquinolones(FQs)have the propensity to accumulate in sediments once introduction into aquatic envi-ronments,thereby posing potential threats to benthic organisms,yet the ecotoxicity of sediment-associated FQs remains unclear.In this study,the toxicokinetics and responses of multiple biomarkers in Bellamya aeruginosa,exposed to the three commonly used FQs(norfloxacin,NOR;ciprofloxacin,CIP;levofloxacin,LEVO)at envi-ronmentally relevant concentrations were investigated under sediment exposure scenario.The results revealed that FQs were effectively ingested by B.aeruginosa from sediments,CIP showing the highest bioaccumulation(180.59μg/kg),followed by NOR(74.49μg/kg)and LEVO(36.02μg/kg).CIP exhibiting a highest uptake rate constant(Ks)(4.64 g/(g·day))and the lowest elimination rate constant(K_(e))(0.05 g/(g·day)).The descending order of biological half-life is as follows:CIP(13.62 days),LEVO(8.14 days),and NOR(6.83 days).NOR induced the activity of superoxide dismutase,catalase,and glutathione-S-transferase while CIP and LEVO depressed their activities and increased malondialdehyde content,indicating a more pronounced oxidative damage to B.aerug-inosa caused by CIP and LEVO than NOR.Furthermore,all three FQs were found to induce DNA damage and elevate acetylcholinesterase activity,suggesting distinct genotoxic and neurotoxic effects.Interestingly,despite its low bioaccumulation potential,LEVO exhibited high toxicity towards B.aeruginosa.These findings enhance our understanding of the ecotoxicity of FQs in sediments,providing further evidence of their potential ecological risks.
文摘The escalating pace of industrialization has significantly intensified water pollution challenges,for instance,the persistent organic pollutants like methyl orange(MO).Conventional remediation techniques,such as adsorption and biological degradation,are often hampered by low efficiency and the risk of secondary pollution.Photocatalysis emerges as a promising sustainable alternative;however,the benchmark material titanium dioxide(TiO_(2))suffers from its intrinsic limitations,notably its wide bandgap energy(≥3.4 eV)restricting its activity to the region of the ultraviolet light and its rapid recombination of photogenerated charge carriers.To overcome these constraints,this research focused on synthesizing novel TiO_(2)/Sn_(3)O_(4) heterojunction composite photocatalysts via a solvothermal approach.Comprehensive characterization techniques confirmed the successful formation of the composite,which revealed that ultrathin Sn3O4 nanosheets uniformly coated TiO_(2) nanospheres.This unique architecture effectively reduced the overall crystallinity and introduced the beneficial oxygen vacancies.Under visible-light irradiation(λ≥420 nm),the optimized TiO_(2)/Sn3O4 composite exhibited the exceptional photocatalytic performance,which achieved 96%degradation of MO within just 60 minutes.The calculated apparent kinetic rate constant(0.103 min^(-1))was remarkably(5.15 times)higher than that of pristine TiO_(2).ESR experiments identified that hydroxyl radicals(·OH)was the predominant active species driving the degradation.Furthermore,cyclic degradation tests demonstrated its excellent material stability,with the composite retaining 85%of its initial efficiency after four consecutive reuse cycles.This work underscored the synergistic effects within the TiO_(2)/Sn_(3)O_(4) heterojunction,which significantly enhanced the visible-light absorption,charge separation,and photocatalytic activity,which provided the valuable insights for designing efficient,stable catalysts for the advanced environmental remediation applications.
基金supported by Natural Science Foundation of Xiamen,China(No.3502Z20227232)the STS Project of Fujian-CAS(No.2023T3018)Bureau of International Cooperation,Chinese Academy of Sciences(No.322GJHZ2022035MI).
文摘Anammox bacteria in constructed wetlands(CWs)play pivotal role in sustainable nitrogen transformation,yet existing studies lack comprehensive analysis of environmental gradients and microbial interactions,both key factors in anammox bacteria enrichment.This study investigated the mechanisms driving anammox bacteria enrichment in lab-scale simulated CWs treating high-nitrogen wastewater,focusing on bacterial community re-sponses across wetland layers with various strategies,including continuous up-flow influent,nitrogen loading increase,effluent recirculation,intermittent influent,and anammox bacteria inoculation.Results showed that total relative and absolute abundances of anammox bacteria ranged from 0.77%to 12.50%and from 0.13 to 6.46×10^(7) copies/g,respectively.Dissolved oxygen and pH had significant positive correlations with the absolute abundance of anammox bacteria,while organic matter and nitrate negatively impacted their relative abundance.Permutational multivariate analysis of variance indicated that spatial heterogeneity explained more variation in anammox bacteria abundance(43.44%)compared to operational strategies(8.58%).In terms of microbial interactions,60 dominant species exhibited potential correlations with anammox bacteria,comprising 170 interactions(105 positive and 65 negative),which suggested that anammox bacteria generally foster cooperative relationships with dominant bacteria.Notably,significant interspecies interactions were observed between Candidatus Kuenenia(dominant anammox bacteria in CWs)and species within the genera Chitinivibrio-nia and Anaerolineaceae,suggesting that microbial interactions primarily manifest as indirect facilitative effects rather than direct mutualistic relationships.Given that the Normalized Stochasticity Ratio in CWs were<50%,this study inferred that environmental gradients have greater influence on anammox bacteria than microbial interactions.
基金supported by the INTERREG ALCOTRA project MITIMPACT,PNRR for Mission 4(Component 2,Notice 3264/2021,IR0000032)-ITINERIS-Italian Integrated Environmental Research Infrastructure System CUP B53C22002150006Project funded under the National Recovery and Resilience Plan(NRRP),Mission 4 Component 2 Investment 1.4-Call for tender No.3138 of December 16,2021,rectified by Decree n.3175 of December 18,2021 of Italian Ministry of University and Research funded by the European Union-NextGenerationEU,Award Number:Project code CN_00000033,Concession Decree No.1034 of June 17,2022 adopted by the Italian Ministry of University and Research,CUP,H43C22000530001 Project title“National Biodiversity Future Center-NBFC”(Spoke 3 and 5)AP and IP were supported by the FOR-CLIMSOC Programme,Project ID PN23090101,financed by the Ministry of Research,Innovation,and Digitization in Romania.
文摘Tropospheric ozone(O_(3))is a harmful air pollutant negatively impacting forest health,causing O_(3)-specific visible foliar injury(O_(3)VFI).Ozone monitoring in forests has usually implemented by passive samplers,although they cannot detect the diurnal peak when a significant part of stomatal O_(3)uptake occurs.This results into uncertainties for the calculation of stomatal O_(3)uptake.This study compares the stomatal-flux-based POD1(phytotoxic ozone dose above a threshold of 1 nmol m^(-2)s^(-1))for forest trees/shrubs estimated from data collected by either passive samplers or active O_(3)monitors to evaluate O_(3)damage to plants in terms of O_(3)VFI in the Southern Alps.The study was conducted over two years(2018-2019)in a mountainous Alpine area(Valle Stura,Italy).An integrative monitoring station for active O_(3)monitoring,as well as passive O_(3)monitors,were installed in an open field area(OFD).The O_(3)VFI was investigated in woody species in the light exposed sampling Site(LESS—Betula pendula,Fagus sylvatica,Larix decidua,Populus tremula,Salix caprea,Rubus sp.and Vaccinium myrtillus)in late summer according to the international co-operative programme on assessment and monitoring of air pollution effects on forests(ICP Forests)manual.The results confirmed that Fagus sylvatica and Rubus sp.are O_(3)-sensitive species showing relatively high POD1(>20 mmol m-2),while Larix decidua is O_(3)-tolerant.We derived flux-based critical levels(CL)corresponding to the presence of O_(3)VFI(5,25,and 50%of symptomatic plants along the LESS)from flux-effect relationships for forest protection against O_(3)VFI.The results support the hypothesis that passive samplers cannot detect episodic high stomatal O₃fluxes(>1 nmol m^(-2)s^(-1)).According to the active monitoring,the CL for O_(3)VFI occurrence was estimated to be 17.1 mmol m-2 POD1 for 25%presence and 34.3 mmol m-2 POD1 for 50%presence of symptomatic plants,while passive samplers underestimated POD1 values for CL calculations by 17%on average,with underestimation increasing at higher CL thresholds.The findings demonstrate that active monitoring refines CLs towards a proper quantitative assessment of O_(3)impact,particularly in capturing peak flux events that are crucial for evaluating plant damage and emphasizes the importance of active O₃monitoring for reliable forest health assessments.
文摘Europe is grappling with a colossal textile waste problem.Over 125 million tonnes of raw materials are devoured by the global industry each year,yet a mere fraction-less than 1%-of these fibres originate from recycled textiles.The majority faces an unsustainable fate in landfills,incinerators,or is exported.A pivotal new report by Systemiq,"The Textile Recycling Breakthrough,"offers both a stark assessment and a strategic roadmap:Europe has the potential to amplify polyester textile recycling nearly tenfold by 2035,but this hinges on immediate,decisive action from policymakers and the industry.
文摘Located on the Qinghai-Xizang Plateau,the Xizang Autonomous Region boasts exceptional solar energy resources.Today,sunlight is being converted into electricity by a 100 megawatt(MW)photovoltaic power station in Chabala Township,Quxu County,Lhasa.Built by Huadian(Quxu)New Energy Co.,Ltd,the project is at an average altitude of 4,000 meters above sea level.It has become a powerful driver of green development in the region,ushering in a new chapter of harmonious coexistence between humanity and nature.
基金supported by the National Natural Science Foundation of China(Nos.62104045,52101213)Jiangsu Provincial Department of Science and Technology of China(No.BE2022426).
文摘As the chemical industry expands,the use of benzene,toluene,and xylene(collectively known as BTX)in industrial production has increased greatly.Meanwhile,the toxic nature and potential health hazards of BTX gases cannot be ignored due to low-concentration leaks underline the critical need for rapid and real-time monitoring of these gases.Chemiresistive metal oxide semiconductor(MOS)-based gas sensors,which are extensively used for gas detection in both industrial settings and everyday life,emerge as one of the optimal solutions for trace BTX detection.These sensors are highly valued for their high sensitivity and low detection limits.Nevertheless,the improvement of selectivity towards specific BTX gases to achieve efficient and precise detection still remains challenging.This review summarizes the chemiresistive MOS-based gas sensors designed for BTX detection,categorizing them based on the components of sensing materials-basically into three groups:single-component,single heterojunction,and multiple heterojunctions gas sensing materials.Further,the review proposes the future application prospects of chemiresistive MOS-based BTX gas sensors,with specific emphasis on their significance in promoting industrial safety and environmental monitoring.
基金supported by the Natural Science Foundation of Hebei Province(No.B2024203026)the Yanzhao Golden Platform Talent Project(Education Platform)of Hebei Province(No.HJYB202517)+1 种基金the National Natural Science Foundation of China(Nos.U22A20403,22006128)the Open Foundation of MOE Key Laboratory of Resources and Environmental System Optimization,College of Environmental Science and Engineering,North China Electric Power University(No.KLRE-KF202308).
文摘Successfully generating reactive oxygen species(ROS)in a targeted and efficient manner for the detoxification of chlorinated organic pollutants(CPs)is a significant and demanding challenge.Herein,we present an in-situ photoreduction strategy to fabricate a composite of palladium(Pd)nanoparticles anchored few-layer carbon nitride nanosheets(Pd-CN).This innovative Pd-CN is then leveraged to activate peroxymonosulfate(PMS)in pursuit of our objective.The incorporation of Pd nanoparticles enhances PMS absorption and targets its terminal oxygen,thereby aiding in the cleavage of the O-O bond.This process generates crucial intermediates,including adsorbed hydroxyl radicals(*OH)and adsorbed atomic oxygen(O*),which are essential for the production of ^(1)O_(2).Consequently,the Pd-CN catalyst demonstrates strong preference for ^(1)O_(2) generation during the PMS activation process,successfully degrading over 95%of pollutants such as 4-chlorophenol(4-CP),2,4-dichlorophenol(2,4-DCP),and 2,4,6-trichlorophenol(2,4,6-TCP)within just 20 min.Additionally,the catalyst exhibits total organic carbon(TOC)removal rates ranging from 49.4%to 31.4%,while the rates for de-chlorination fall between 68.6%and 72.7%.A subsequent continuous-flow treatment experiment has confirmed the application potential of this system,demonstrating consistent catalytic activity for up to 8 h.This promising technique presents an efficient strategy for addressing the high toxicity of chlorinated organic pollutants in contaminated water.
文摘Triclosan(TCS) poses harmful risks to ecosystems and human health owing to its endocrine-disrupting effects.Therefore,developing an efficient and sustainable technology to degrade TCS is urgently needed.Herein,cobalt oxyhydroxide @covalent organic frameworks(CoOOH@COFs) S-scheme heterojunction was synthesized,which combined the visible-light-driven photocatalysis and peroxymonosulfate(PMS) activation to synergistically generate abundant reactive oxygen species(ROSs) for TCS degradation.The degradation efficiency of TCS reached 100 % within 8 min in the Vis-CoOOH@COFs/PMS system,and the reaction rate constant was 0.456 min^(-1),which was nearly 1.90 and 2.85 times that of single Co OOH and COFs,and2.36 times that under dark condition,respectively.The density functional theory(DFT) calculations confirmed the energy band bending of CoOOH@COFs and S-scheme charge transport from COFs to Co OOH.Both experimental and theoretical analyses indicated that Co OOH@COFs in photocatalytic-PMS activation systems synergistically facilitated photo-generated carrier separation,enhanced interfacial electron transfer,accelerated PMS activation,and generated multiple ROSs.In particular,photogenerated electrons(e^(-))accelerated the Co(Ⅲ)/Co(Ⅱ) redox cycle,while the PMS captured the e-,which significantly decreased the charge combination of Co OOH@COFs.Radicals(O_(2)^(·-),^(·)OH,and SO_(4)^(·-)) and non-radicals(such as ^(1)O_(2),h^(+),and e^(-)) were both presented in the Vis-CoOOH@COFs/PMS system,with O_(2)^(-) playing a dominant role in TCS degradation.Furthermore,the pathway of TCS degradation and toxicity of intermediates were explored by DFT calculation and transformation product identification.Importantly,the environmentally friendly CoOOH@COFs S-scheme heterojunction exhibited excellent stability and reusability.In conclusion,this study innovatively designed an S-scheme heterojunction in the photocatalytic-PMS activation system,providing guidance and theoretical support for efficient and eco-friendly wastewater treatment.
基金supported by the National Natural Science Foundation of China(No.41975156)and the Fundamental Research Funds for the Central Universities.
文摘Oxidative potential(OP)can be used as an indicator of the health risks of particulate matter in the air.To study the variation and sources of OP,we conducted an observation of PM_(2.5) in a megacity in southern China in winter and spring of 2021.The results show that the average concentration of PM_(2.5) decreased by 47%from winter to spring,while volume-normalized and mass-normalized OP(i.e.,OP_(v) and OP_(m))increased by 6%and 69%,respectively.It suggests that the decline of PM_(2.5) may not necessarily decrease the health risks and the intrinsic toxicity of PM_(2.5).Variations of OP_(v) and OP_(m) among different periods were related to the different source contributions and environmental conditions.The positive matrix factorization model was used to identify the major sources of OP_(v).OP_(v) was mainly contributed by biomass burning/industrial emissions(29%),soil/road dust(20%),secondary sulfate(14%),and coal combustion(13%)in winter.Different major sources were resolved to be secondary sulfate(36%),biological sources(21%),and marine vessels(20%)in spring,presenting the substantial contribution of biological sources.The analysis shows strong associations between OP_(v) and both live and dead bacteria,further confirming the important contribution of bioaerosols to the enhancement of OP.This study highlights the importance of understanding OP in ambient PM_(2.5) in terms of public health impact and provides a new insight into the biological contribution to OP.
基金Supported by The Central Public-Interest Scientific Institution Basal Research Fund,CAFS(2025XT0902)Earmarked for China Agriculture Research System(CARS-46).
文摘The widespread use of herbicides such as glyphosate isopropyl amine salt(GIS)and atrazine(ATZ)poses significant risks to aquatic ecosystems.This study investigated the single and joint acute toxicity of a 1:1 GIS-ATZ mixture on zebrafish(Danio rerio).Acute tests determined 96-h LC_(50) values of 123.41 mg/L for GIS and 103.95 mg/L for ATZ.In the joint toxicity test,these values decreased to 60.96 and 50.88 mg/L,respectively.The Additive Index(AI)analysis revealed a consistent synergistic interaction between the herbicides at all exposure intervals.These findings underscore the enhanced ecological threat of herbicide mixtures and highlight the necessity of considering joint effects in environmental risk assessments.
基金supported by the National Key R&D Program of China (Grant No.2025YFE0100700)the National Natural Science Foundation of China (Grant No.52270138)the International Science and Technology Cooperation Program of Shanghai Science and Technology Innovation Action Plan (Grant No.22230712200)。
文摘Biochar, known as “black gold”, has garnered wide attention in various applications. However, the potential release of toxic organic compounds has raised environmental concerns, thereby limiting its safe and sustainable application. Herein, we propose a distillation strategy to simultaneously detoxify biochar and enhance its redox functionality. Multi-factor correlation analysis identified 30 min as the optimal distillation time, which significantly increased the biochar's Brunauer-Emmett-Teller(BET) surface area(by 143%), improved hydrophilicity(with contact angle decreased by 3.8%), and effectively reduced the dissolved organic carbon(DOC) content of the biochar. Regarding the effect of distillation solvent, both water and acetic acid significantly enhanced the electron exchange capacity(EEC) of the biochar, with lactic acid exhibiting the best performance in improving the electron donating capacity(EDC). Meanwhile, distillation with acetic acid achieved optimal detoxification by effectively removing toxic organic compounds such as naphthalene, amines, and aromatic hydrocarbons. Further validation confirmed the good generalizability of this method to biochars derived from various feedstocks. Techno-economic analysis showed a 98.7% reduction in water consumption and 22.9%-62.5% cost savings compared to traditional washing methods. This work highlights distillation as an efficient, eco-friendly, and cost-effective method to enhance biochar safety and redox functionality, thereby advancing its sustainable applications.
