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Dissolved inorganic nitrogen as an overlooked precursor of nitrogenous disinfection byproducts - A critical review 作为含氮消毒副产物的一种被忽视的前体的溶解无机氮--重要评论
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122654
Xiao Li, Tom Bond, Xiaoyu Tan, Haolin Yang, Yuheng Chen, Bingbing Jin, Baiyang Chen
Aquatic nitrogenous compounds can be classified as dissolved organic nitrogen (DON) and dissolved inorganic nitrogen (DIN), including ammonia, nitrite, nitrate, and inorganic chloramines. The occurrence of nitrogenous disinfection byproducts (N-DBPs) in water, such as haloacetonitriles (HANs), halonitromethanes (HNMs), haloacaetamides (HAcAms), and nitrosamines (NAs), has attracted considerable attention due to their higher toxicity than regulated carbonaceous analogues. While numerous studies have investigated the contributions of DON to N-DBP formation, relatively fewer studies have explored DIN as N-DBP precursors, although DINs are sometimes evaluated as influencing factors. Through a literature review and data mining, this study delves into the existing body of evidence that analyze the contributions of different forms of DIN to N-DBP generation. The results showed that ammonia and nitrite can enhance trichloronitromethane (TCNM) and nitrodimethylamine (NDMA) formation in conventional chlorination and chloramination processes, nitrate can promote HNM formation in ultraviolet-based processes, and monochloramine can increase HAN, HAcAm, HNM, and NDMA formation in most disinfection scenarios. Notably, some experiments demonstrated that the yields of dichloroacetonitrile (DCAN) and TCNM can be higher from reactions involving nitrogen-free organic precursors and DIN than those involving DON and nitrogen-free disinfectant, suggesting that the relative importance of DON and DIN in forming N-DBP in real water remains unresolved. These insights thus underscore DIN as a non-negligible precursor in N-DBP formation and call for more attention to water management strategies for DIN.
水生含氮化合物可分为溶解有机氮 (DON) 和溶解无机氮 (DIN),包括氨、亚硝酸盐、硝酸盐和无机氯胺。水中出现的含氮消毒副产物(N-DBPs),如卤代乙腈(HANs)、卤代硝基甲烷(HNMs)、卤代乙酰胺(HAcAms)和亚硝胺(NAs),因其毒性高于受管制的碳质类似物而备受关注。尽管有许多研究调查了 DON 对 N-DBP 形成的贡献,但探讨 DIN 作为 N-DBP 前体的研究相对较少,尽管 DIN 有时也被评估为影响因素。通过文献综述和数据挖掘,本研究深入研究了现有的证据,分析了不同形式的 DIN 对 N-DBP 生成的贡献。结果表明,在传统氯化和氯化工艺中,氨和亚硝酸盐可促进三氯硝基甲烷(TCNM)和硝基二甲胺(NDMA)的形成;在基于紫外线的工艺中,硝酸盐可促进 HNM 的形成;在大多数消毒方案中,一氯胺可增加 HAN、HAcAm、HNM 和 NDMA 的形成。值得注意的是,一些实验表明,与涉及 DON 和无氮消毒剂的反应相比,涉及无氮有机前体和 DIN 的反应产生的二氯乙腈 (DCAN) 和 TCNM 的产量更高,这表明 DON 和 DIN 在实际水中形成 N-DBP 的相对重要性仍未得到解决。因此,这些见解强调 DIN 是 N-DBP 形成过程中不可忽视的前体,并呼吁更多地关注 DIN 的水管理策略。
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引用次数: 0
Pharmaceuticals in urban streams: a review of their detection and effects in the ecosystem 城市溪流中的药物:关于其在生态系统中的检测和影响的综述
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122657
Fernanda Rodrigues, Luisa Durães, Nuno E.C. Simões, André M. P.T. Pereira, Liliana J.G. Silva, Maria João Feio
The presence of pharmaceuticals in urban freshwater has been considered an emerging issue. Although rivers are better studied, the streams crossing the cities, which are prone to higher concentrations of pharmaceuticals, and with a higher potential to affect animals, plant and human health, were never specifically addressed in a review. Thus, here we performed a literature review on the existing pharmaceutical contamination and impacts of these compounds in the urban stream ecosystems. To structure the review, 10 questions were designed. From a total of 206 scientific publications, only 51 addressed the issue of pharmaceuticals in urban streams compared to 180 studies in the larger urban rivers. In 49 urban streams located in 13 countries and four continents, 139 pharmaceuticals from ten therapeutic groups were found. Anti-inflammatories and anticonvulsants were detected in the largest number of countries and urban streams, but the latter was more frequent in the streams. Metabolites were also detected, sometimes in higher concentrations than the original pharmaceutical but they were seldom analysed. The pharmaceuticals that caused more effects in the aquatic organisms were 17β-estradiol, estriol, estrone, acetaminophen, caffeine, carbamazepine, diltiazem, diphenhydramine, fluoxetine, norfluoxetine, sertraline, desmethylsertraline, methylphenidate and ciprofloxacin. The effects were varied, from bioaccumulation, endocrine disruption, impaired growth, reproduction inhibition, increased mortality and hatching disorder to morphological alterations, and decreased gross primary production and biomass. Streams had a higher mixture risk compared to the rivers. Important knowledge gaps detected are the low frequency of analysis of metabolites, the inefficient treatment of urban sewage regarding pharmaceuticals and the reduced number of studies on the impacts of pharmaceuticals at the aquatic community/population and functional level.
城市淡水中的药物被认为是一个新出现的问题。虽然对河流的研究较多,但对穿越城市的溪流的研究却很少,因为这些溪流中的药物浓度较高,影响动物、植物和人类健康的可能性也较大。因此,我们在此对城市溪流生态系统中现有的药物污染及其影响进行了文献综述。为了构建综述的结构,我们设计了 10 个问题。在总共 206 篇科学出版物中,只有 51 篇涉及城市溪流中的药物问题,而针对城市大河的研究则有 180 篇。在四大洲 13 个国家的 49 条城市河流中,发现了来自 10 个治疗组的 139 种药物。在最多的国家和城市溪流中发现了消炎药和抗惊厥药,但后者在溪流中更为常见。还检测到了代谢物,有时其浓度高于原药,但很少对其进行分析。对水生生物影响较大的药物有:17β-雌二醇、雌三醇、雌酮、对乙酰氨基酚、咖啡因、卡马西平、地尔硫卓、苯海拉明、氟西汀、氟西汀、舍曲林、去甲舍曲林、哌醋甲酯和环丙沙星。其影响多种多样,包括生物蓄积、内分泌紊乱、生长受损、繁殖抑制、死亡率上升、孵化障碍、形态改变、初级生产总量和生物量下降等。与河流相比,溪流的混合物风险更高。所发现的重要知识缺口包括:代谢物分析频率低、城市污水中药物处理效率低,以及关于药物在水生群落/种群和功能层面影响的研究较少。
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引用次数: 0
Adsorption of oxidized humic acid onto redox-inert mineral surfaces induces formation of hydroxyl radicals and carbon dynamics 氧化腐植酸在氧化还原惰性矿物表面的吸附诱导形成羟基自由基和碳动力学
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122653
Shengyan Pu, Xinyi Li, Zhongquan Liu, Peng Zhang, Chenglong Yu
The dark formation of hydroxyl radicals (•OH) from O2 activation by reduced humic substances at oxic-anoxic interfaces has been extensively documented. However, their generation in oxic subsurface environments is typically overlooked due to the scarcity of electron donors, especially in the presence of minerals. In this study, the formation of •OH during the adsorption of oxidized humic acids (HA) onto redox-inert minerals was investigated under oxic and pH-neutral conditions. Batch experiment results demonstrated that the adsorption of oxidized HA onto aluminum (hydr)oxide and Fe-free clay minerals induces the formation of •OH (e.g., 16/28 μmol/g C) without the addition of exogenous electron donors. In contrast, the interaction of oxidized HA alone with O2 did not result in measurable •OH production. The enhanced electron-donating capacity (EDC) and humification of the whole HA (mainly in adsorbed state) were measured after adsorption. The surface-catalyzed polymerization of oxidizable polyphenols in HA is proposed as the plausible mechanism for the observed EDC enhancement, which in turn triggers O2 activation for •OH production. Furthermore, substantial chemical alterations of lignins and condensed aromatics within HA were observed, producing more compounds exhibiting higher molecular weight, aromaticity, O/C ratio, and nominal oxidation state of carbon. It is indicated that the contribution of oxidative polymerization outweighs •OH oxidation in the molecular transformation of adsorbed HA. Overall, our findings extend the understanding of HA-induced •OH production from oxic-anoxic interfaces to the oxic zone and present a novel pathway for the abiotic transformation of recalcitrant organic matter in subsurface environments with extensive surface water-groundwater interactions.
在缺氧-缺氧界面上,还原腐殖质在氧气活化作用下暗中形成羟基自由基(-OH)的现象已被广泛记录。然而,由于缺乏电子供体,尤其是在矿物存在的情况下,它们在含氧地下环境中的生成通常被忽视。本研究调查了氧化腐植酸(HA)在氧化和 pH 值中性条件下吸附在氧化还原惰性矿物上过程中 -OH 的形成。批量实验结果表明,氧化型腐植酸吸附在氧化铝(水)和无铁粘土矿物上时,在不添加外源电子供体的情况下会形成-OH(例如,16/28 μmol/g C)。与此相反,氧化的HA单独与O2相互作用不会产生可测量的-OH。在吸附后,还测量了增强的电子供体能力(EDC)和整个HA(主要是吸附状态)的腐殖化。据推测,HA 中可氧化多酚的表面催化聚合是导致所观察到的 EDC 增强的合理机制,而 EDC 的增强反过来又会引发 O2 激活以产生 -OH。此外,还观察到 HA 中的木质素和缩合芳烃发生了重大化学变化,产生了更多分子量、芳香度、O/C 比和碳的名义氧化态更高的化合物。这表明,在吸附 HA 的分子转变过程中,氧化聚合的作用超过了-OH 氧化的作用。总之,我们的研究结果将人们对 HA 诱导的 -OH 生成的理解从缺氧-缺氧界面扩展到了缺氧区,并为地表水-地下水相互作用广泛的地下环境中难降解有机物的非生物转化提供了一条新途径。
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引用次数: 0
Methylmercury degradation by hot spring sulfur-linked microbial communities as a dominant pathway in regulating mercury speciation 温泉硫链微生物群落对甲基汞的降解是调节汞标示的主要途径
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122652
Jin-Ping Xue, Rosanna Margalef-Marti, Aubin Thibault De Chanvalon, Emmanuel Tessier, Rémy Guyoneaud, Zoyne Pedrero, Claire Gassie, Mathieu Sebilo, Michael S. Bank, David Amouroux
Sulfidic hot springs harbor unique microbial communities and are important in mercury (Hg) species transformations, although the fine scale drivers of these processes remain poorly understood. Here we studied Hg speciation in water, biofilms, and sediment across three sampling seasons in a French sulfidic hot spring with low Hg concentrations. Microbial Hg species methylation and demethylation potentials were evaluated using incubation experiments with species-specific Hg isotope tracers. Temporal variation in inorganic Hg (iHg) and methylmercury (MeHg) concentrations in water, biofilm, and sediment was observed. The incubation of microbial communities in biofilms and sediment under dark conditions exhibited low iHg methylation potentials, whereas a significant extent of biotic MeHg demethylation to oxidized iHg was found in relation to MeHg concentrations. Results from microbial diversity (16S rDNA) and the metabolic inhibition experiments suggest an important role of sulfur-linked bacterial metabolism dynamics. Specifically, sulfate-reducers and anoxygenic phototrophs were important factors in the regulation of MeHg concentrations in our study site. Overall, the observed dominance of microbial MeHg demethylation demonstrates a strong Hg detoxification capacity in sulfidic aquatic environments.
硫化温泉蕴藏着独特的微生物群落,在汞(Hg)物种转化过程中起着重要作用,但人们对这些过程的精细驱动因素仍然知之甚少。在这里,我们研究了法国一个汞浓度较低的硫酸型温泉在三个采样季节中水、生物膜和沉积物中的汞分类。通过使用物种特异性汞同位素示踪剂进行培养实验,评估了微生物汞物种甲基化和脱甲基化的潜力。观察了水、生物膜和沉积物中无机汞(iHg)和甲基汞(MeHg)浓度的时间变化。生物膜和沉积物中的微生物群落在黑暗条件下的培养显示出较低的 iHg 甲基化潜能,而生物甲基汞脱甲基化为氧化 iHg 的程度与甲基汞浓度有关。微生物多样性(16S rDNA)和代谢抑制实验的结果表明,与硫有关的细菌代谢动态起着重要作用。具体来说,硫酸盐还原菌和无氧光养菌是调节研究地点甲基汞浓度的重要因素。总之,所观察到的微生物甲基汞脱甲基作用的优势表明,硫酸型水生环境具有很强的汞解毒能力。
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引用次数: 0
Making Waves: The Progress of Management Strategies for Cleaning and Rinsing of PFAS-Impacted Fire Suppression Systems 掀起波澜:受 PFAS 影响的灭火系统清洗和冲洗管理策略的进展情况
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122661
Hooman Vatankhah, Richard H. Anderson, Rajat Ghosh, Janice Willey, Andrea Leeson
Aircraft rescue firefighting (ARFF) vehicles often contain residual levels of per- and polyfluoroalkyl substances (PFAS) due to the global use of legacy and current use of aqueous film-forming foam (AFFF) for class B firefighting. However, numerous countries are transitioning to fluorine-free foam (F3) alternatives. There is, thus, an urgent need to develop efficient methods to rinse and clean interior ARFF surfaces thereby avoiding expensive replacement costs and preventing further discharge of PFAS to the environment. However, the unique self-assembly behavior of amphiphilic PFAS is a complicating factor that can result in measurable levels of PFAS within replacement F3s following cleanout efforts (i.e., the rebound effect). This Making Waves article aims to elucidate the emerging challenges associated with cleanout of impacted ARFF vehicles and introduce the current efforts for PFAS management of rinsate derived from cleanout of impacted fire suppression infrastructure.
由于全球都在使用传统的水成膜泡沫(AFFF)进行 B 级灭火,因此飞机救援消防(ARFF)车辆通常都含有残留的全氟和多氟烷基物质(PFAS)。然而,许多国家正在向无氟泡沫(F3)替代品过渡。因此,迫切需要开发有效的方法来冲洗和清洁 ARFF 内部表面,从而避免昂贵的更换费用,并防止 PFAS 进一步排放到环境中。然而,两亲性 PFAS 独特的自组装行为是一个复杂因素,可能导致在清理工作结束后,替换 F3 内的 PFAS 含量达到可测量的水平(即反弹效应)。这篇 "兴风作浪 "的文章旨在阐明与清理受影响的 ARFF 车辆相关的新挑战,并介绍目前对清理受影响的灭火基础设施所产生的冲洗液进行 PFAS 管理的工作。
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引用次数: 0
Bacterial hosts and horizontal transfer characteristics of clinically important tet(X)-variant genes in municipal wastewater treatment plants using epicPCR-directed cultivation strategy 利用 epicPCR 引导培养策略研究城市污水处理厂中临床重要的 tet(X) 变异基因的细菌宿主和水平转移特征
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122658
Shiting Dai, Ziming Han, Shihai Liu, Yang Wang, Yu Zhang, Min Yang
Mobile tet(X)-variant genes confer resistance to a wide range of tetracyclines, including the antibiotic of last-resort, tigecycline, raising significant concerns regarding their potential spread cross-environmental dissemination. However, the bacterial hosts and environmental spread of these genes remain poorly understood. Herein, a retrospective study unveiled the prevalence of tet(X)-variant genes (ranging from tet(X3) to tet(X6)) in activated sludge samples from five municipal wastewater treatment plants (WWTPs) from 2013 to 2021. Among these variants, tet(X4) exhibited the highest detection frequency (100%) and abundance [(2.48 ± 3.07) × 107 copies/g dry weight] with an increasing trend. An epicPCR-directed cultivation strategy was proposed to facilitate the targeted isolation of tet(X4)-carrying bacterial hosts in activated sludge. This strategy involves the identification of bacterial host profiles using epicPCR and subsequent selective isolating target bacteria. Enterobacteriaceae emerged as the primary bacterial host for tet(X4), alongside previously unreported genera like Providencia, Advenella, and Moheibacter. Subsequent selective isolation of the most abundant Enterobacteriaceae based on the epicPCR-informed host spectrum yielded 39 tet(X4)-carrying Escherichia coli strains from the WWTP. Whole genome sequencing of tet(X4)-positive strains revealed that plasmid-mediated horizontal gene transfer is the primary mechanism driving tet(X4) dissemination. Plasmids including IncFIA(HI1)/IncHI1A/IncHI1B(R27) and IncX1, commonly reported in various clinical and animal settings, were identified as the predominant carriers of tet(X4). E. coli strains harbouring tet(X4) in the WWTP showed substantial genetic similarity to strains from hospital and animal sources, underscoring concerns about the potential risk of across diverse sectors. This study provided the first glimpse of the presence of mobile tet(X)-variants in WWTPs, and highlighted the promise of the epicPCR-directed cultivation strategy for exploring bacterial hosts of clinically important ARGs in different habitats from a One Health perspective.
可移动的 tet(X)变异基因对多种四环素类药物(包括最后的抗生素替加环素)具有抗药性,这引起了人们对其跨环境传播潜力的极大关注。然而,人们对这些基因的细菌宿主和环境传播仍然知之甚少。在本文中,一项回顾性研究揭示了2013年至2021年期间五个城市污水处理厂(WWTPs)活性污泥样本中的tet(X)变体基因(从tet(X3)到tet(X6)不等)的流行情况。在这些变体中,tet(X4)的检测频率(100%)和丰度[(2.48 ± 3.07)×107拷贝/克干重]最高,且呈上升趋势。为便于有针对性地分离活性污泥中携带 tet(X4) 的细菌宿主,提出了一种 epicPCR 引导的培养策略。该策略包括使用 epicPCR 鉴定细菌宿主特征,然后选择性分离目标细菌。肠杆菌科成为 tet(X4) 的主要细菌宿主,此外还有普罗维登斯属、阿文氏菌属和莫氏菌属等以前未报道过的菌属。随后,根据 epicPCR 信息宿主谱对最丰富的肠杆菌科细菌进行选择性分离,从污水处理厂中分离出 39 株携带 tet(X4) 的大肠埃希菌。对 tet(X4) 阳性菌株的全基因组测序显示,质粒介导的水平基因转移是驱动 tet(X4) 传播的主要机制。包括 IncFIA(HI1)/IncHI1A/IncHI1B(R27) 和 IncX1 在内的质粒是 tet(X4) 的主要携带者,这些质粒通常在各种临床和动物环境中被报道。污水处理厂中携带 tet(X4)的大肠杆菌菌株与医院和动物来源的菌株在基因上有很大的相似性,这突显了对不同行业潜在风险的担忧。这项研究首次揭示了污水处理厂中存在的移动 tet(X)变体,并强调了 epicPCR 引导培养策略的前景,该策略可从 "一体健康 "的角度探索不同生境中临床上重要的 ARGs 的细菌宿主。
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引用次数: 0
Role of biogeochemical and hydrodynamic characteristics in simulating nitrogen dynamics in river confluence 生物地球化学和水动力特征在模拟河流汇流处氮动态中的作用
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122647
The confluence area is the link of different river systems, whose specific hydrodynamic characteristics can significantly influence mass transport and…
汇流区是不同河流水系的连接点,其特定的水动力特性会极大地影响河流的质量输运和水流的速度。
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引用次数: 0
Removal of per- and polyfluoroalkyl substances (PFAS) from municipal wastewater by foam fractionation 通过泡沫分馏去除城市污水中的全氟和多氟烷基物质 (PFAS)
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122660
Andriy Malovanyy, Erika Forsén, Richard Lihammar
Municipal wastewater has a relatively low content of per- and polyfluoroalkyl substances (PFAS), compared with other point sources such as landfill leachate and industrial effluents. Nevertheless, it is considered as one of the major point pollution sources. Foam fractionation was previously shown to effectively remove PFAS from different water matrices and to reach a high PFAS enrichment. In this study, the removal of PFAS from municipal wastewater of different origins was investigated. Despite the low foaming potential, it was possible to reach an average removal of the sum of perfluorooctanesulfonic acid (PFOS), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorohexanesulfonic acid (PFHxS) of 93%, the removal of the sum of 21 PFAS of 56%, and the removal of the sum of PFAS expressed as PFOA equivalents (ΣPFOAeq) of 91%, without any surfactant addition utilizing a novel approach of foam collection. The PFAS content was reduced to below the limit values for drinking water in Sweden and the anticipated future limit values for surface water in the European Union. The addition of four commercial surfactants and an extract of extracellular polymeric substances (EPS) from waste activated sludge each enhanced the foam formation. Moreover, a cationic surfactant increased the removal of short-chain PFAS. Additionally, foam fractionation of activated sludge was performed. A considerably lower ΣPFOAeq removal of only 20% was demonstrated, which was explained by a high proportion of PFAS sorbed to sludge. Finally, the study discusses the practical implications of the application of foam fractionation at municipal wastewater treatment plants.
与垃圾填埋场沥滤液和工业废水等其他点污染源相比,城市污水中的全氟和多氟烷基物质 (PFAS) 含量相对较低。尽管如此,它仍被视为主要的点污染源之一。之前的研究表明,泡沫分馏法能有效去除不同水基质中的 PFAS,并达到较高的 PFAS 富集度。本研究调查了从不同来源的城市污水中去除 PFAS 的情况。尽管发泡潜能较低,但全氟辛烷磺酸(PFOS)、全氟辛酸(PFOA)、全氟壬酸(PFNA)和全氟己烷磺酸(PFHxS)的平均去除率达到了 93%、利用一种新型泡沫收集方法,在不添加任何表面活性剂的情况下,21 种 PFAS 的去除率为 56%,以 PFOA 当量(ΣPFOAeq)表示的 PFAS 去除率为 91%。PFAS 的含量被降低到低于瑞典饮用水的限值和欧盟地表水的预期限值。添加四种商用表面活性剂和一种从废弃活性污泥中提取的细胞外高分子物质(EPS)都能增强泡沫的形成。此外,阳离子表面活性剂还能提高短链 PFAS 的去除率。此外,还对活性污泥进行了泡沫分馏。结果表明,ΣPFOAeq 的去除率大大降低,仅为 20%,原因是吸附在污泥中的 PFAS 比例较高。最后,该研究讨论了在城市污水处理厂应用泡沫分馏技术的实际意义。
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引用次数: 0
Feedstock-dependent antibiotic resistance gene patterns and expression profiles in industrial scale biogas plants revealed by meta-omics technology 元组学技术揭示工业规模沼气厂中原料依赖性抗生素耐药基因模式和表达谱
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122650
Roland Wirth, Prateek Shetty, Zoltán Bagi, Kornél L. Kovács, Gergely Maróti
This study investigated antimicrobial resistance in the anaerobic digesters of two industrial-scale biogas plants processing agricultural biomass and municipal wastewater sludge. A combination of deep sequencing and genome-centric workflow was implemented for metagenomic and metatranscriptomics data analysis to comprehensively examine potential antimicrobial resistance in microbial communities. Anaerobic microbes were found to harbour numerous antibiotic resistance genes (ARGs), with 58.85% of the metagenome-assembled genomes (MAGs) harbouring antibiotic resistance. A moderately positive correlation was observed between the abundance and expression of ARGs. ARGs were located primarily on bacterial chromosomes. A higher expression of resistance genes was observed on plasmids than on chromosomes. Risk index assessment suggests that most ARGs identified posed a significant risk to human health. However, potentially pathogenic bacteria showed lower ARG expression than non-pathogenic ones, indicating that anaerobic treatment is effective against pathogenic microbes. Resistomes at the gene category level were associated with various antibiotic resistance categories, including multidrug resistance, beta-lactams, glycopeptides, peptides, and macrolide-lincosamide-streptogramin (MLS). Differential expression analysis revealed specific genes associated with potential pathogenicity, emphasizing the importance of active gene expression in assessing the risks associated with ARGs.
本研究调查了两个处理农业生物质和城市污水污泥的工业规模沼气厂厌氧消化池中的抗菌素耐药性。该研究结合深度测序和以基因组为中心的工作流程,对元基因组学和元转录组学数据进行分析,以全面研究微生物群落中潜在的抗菌药耐药性。研究发现厌氧微生物携带大量抗生素耐药性基因(ARGs),58.85%的元基因组组装基因组(MAGs)携带抗生素耐药性。ARGs的丰度和表达之间呈中度正相关。ARGs 主要位于细菌染色体上。与染色体相比,质粒上抗性基因的表达量更高。风险指数评估表明,大多数已发现的 ARGs 对人类健康构成重大风险。不过,潜在致病菌的 ARG 表达量低于非致病菌,这表明厌氧处理对致病微生物是有效的。在基因类别水平上,耐药性基因组与各种抗生素耐药性类别有关,包括多重耐药性、β-内酰胺类、糖肽类、肽类和大环内酯-林可酰胺-链霉亲和素(MLS)。差异表达分析揭示了与潜在致病性相关的特定基因,强调了活性基因表达在评估 ARGs 相关风险中的重要性。
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引用次数: 0
Shell-induced enhancement of Fenton-like catalytic performance towards advanced oxidation processes: concept, mechanism, and properties 贝壳诱导增强芬顿催化性能以实现高级氧化过程:概念、机理和特性
IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-10-18 DOI: 10.1016/j.watres.2024.122655
Yuezhu Wang, Mengxiao Zhong, Fuqiu Ma, Ce Wang, Xiaofeng Lu
Fenton-like advanced oxidation processes (AOPs) are commonly used to eliminate recalcitrant organic pollutants as they produce highly reactive oxygen species through the reactions between the catalysts and oxidants. Recently, considerable attention has been directed towards shell-structured Fenton-like catalysts that offer high stability, maximum utilization of active sites, and exceptional catalytic performance. In this review, we have introduced the concept of several typical shell-forming architectures (e.g., hollow structure, core-shell structure, yolk-shell structure, particle-in-tube structure, and multi-shelled structure), elucidating their role in promoting Fenton-like reaction catalysis through the nanoconfinement mechanism. In each aspect, the correlation between the shell-induced effects and the Fenton-like catalytic performance is highlighted. Finally, future challenges and opportunities for the development of shell-structured Fenton-like catalysts towards AOPs are presented, offering bright practical application prospects.
类似芬顿的高级氧化工艺(AOPs)通过催化剂和氧化剂之间的反应产生高活性氧物种,通常用于消除难降解的有机污染物。最近,人们开始关注具有高稳定性、活性位点利用率最大化和优异催化性能的壳结构 Fenton 类催化剂。在这篇综述中,我们介绍了几种典型的成壳结构(如中空结构、核壳结构、卵黄壳结构、管内颗粒结构和多壳结构)的概念,阐明了它们通过纳米融合机制在促进 Fenton 类反应催化中的作用。每个方面都强调了壳诱导效应与 Fenton 类催化性能之间的相关性。最后,介绍了未来开发壳结构 Fenton 类催化剂的挑战和机遇,为 AOPs 提供了广阔的实际应用前景。
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