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Resourceful treatment of complex uranium-organic wastewater by a hybrid tandem photocatalytic fuel cell with SnS2 nanoplate modified carbon felt cathode 采用 SnS2 纳米板修饰碳毡阴极的混合串联光催化燃料电池资源化处理复杂的铀有机废水
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-19 DOI: 10.1016/j.jhazmat.2024.135861
Rongzhong Wang , Yaqian Zhang , Xuemei Sun , Qingyan Zhang , Zhaowen Cheng , Wenjing Xue , Qingyi Zeng

Resourceful treatment of wastewater is a promising way to facilitate sustainable development. Recently, photocatalytic fuel cells (PFCs) have attracted widespread attention as the method that can synchronously achieve wastewater treatment and clean energy production only depend on light. However, few PFCs focused on treating complex uranium (U(VI))-organic wastewater. This study prepared a SnS2 nanoplate decorated carbon felt (SnS2/CF) material by facile hydrothermal method and used as the cathode to construct a hybrid tandem photocatalytic fuel cell (HTPFC) system. Compared to the CF-HTPFC, the removal efficiencies of U(VI) and tetracycline hydrochloride (TCH) increased to 3.4 and 1.8 times in the SnS2/CF-HTPFC system, accompanied with the reaction rate (kobs) values increased to 30.39 and 3.78 times, respectively. More importantly, under real sunlight irradiation (From 10:00 to 16:00), the removal efficiencies of U(VI) and TCH respectively reached 92.49 % and 97.96 %, and the Pmax reached 6.49 mW·cm−2. HTPFC also displayed satisfactory performances in treating radioactive wastewater containing different organic compounds, with the removal efficiencies of U(VI) and organic compounds both exceeded 93.35 %. The loading of SnS2 nanoplates enhanced electrochemical performance and introduced abundant S active sites, allowing more U(VI) to be adsorbed and reduced, and simultaneously promoting the removal of organic matter by improving the charge separation efficiency.

废水资源化处理是促进可持续发展的一条大有可为的途径。最近,光催化燃料电池(PFCs)作为一种仅依靠光就能同步实现废水处理和清洁能源生产的方法引起了广泛关注。然而,很少有 PFC 专注于处理复杂的铀 (U(VI)) 有机废水。本研究采用简便的水热法制备了SnS2纳米板装饰碳毡(SnS2/CF)材料,并以此为阴极构建了混合串联光催化燃料电池(HTPFC)系统。与 CF-HTPFC 相比,SnS2/CF-HTPFC 系统对 U(VI)和盐酸四环素(TCH)的去除率分别提高了 3.4 倍和 1.8 倍,反应速率(kobs)值也分别提高了 30.39 倍和 3.78 倍。更重要的是,在实际日光照射下(10:00 至 16:00),U(VI)和 TCH 的去除率分别达到 92.49 % 和 97.96 %,Pmax 达到 6.49 mW-cm-2。HTPFC 在处理含有不同有机化合物的放射性废水时也表现出令人满意的性能,对 U(VI)和有机化合物的去除率均超过 93.35%。SnS2纳米板的负载增强了电化学性能,并引入了丰富的S活性位点,使更多的U(VI)被吸附和还原,同时通过提高电荷分离效率促进了有机物的去除。
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引用次数: 0
Tracking chemical feature releases from plastic food packaging to humans 追踪塑料食品包装向人类释放的化学特征
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-18 DOI: 10.1016/j.jhazmat.2024.135897
Weikun Meng , Qianyu Chen , Yayun Zhang , Hao Sun , Jianhua Li , Hong Sun , Chunsheng Liu , Mingliang Fang , Guanyong Su

Humankind are being exposed to a cocktail of chemicals, such as chemicals released from plastic food packaging. It is of great importance to evaluate the prevalence of plastic food packaging-derived chemicals pollution along the flow of food-human. We developed a robust and practical database of 2101 chemical features associated with plastic food packaging that combined data from three sources, 925 of which were acquired from non-target screening of chemical extracts from eight commonly used plastic food packaging materials. In this database, 625 features, especially half of the non-targets, were potential migrants who likely entered our bodies through dietary intake. Biomonitoring analysis of plastic chemical features in foodstuffs or human serum samples showed that approximately 78 % of the 2101 features were detectable and approximately half were non-targets. Of these, 17 plastic chemicals with high detection frequencies (DFs) in the human serum were confirmed to be functional chemical additives. Together, our work indicates that the number of plastic chemicals in our bodies could be far greater than previously recognized, and human exposure to plastic chemicals might pose a potential health risk.

人类正暴露于各种化学物质,如塑料食品包装释放的化学物质。评估食品-人类流动过程中由塑料食品包装产生的化学品污染的普遍程度具有重要意义。我们开发了一个强大而实用的数据库,其中包含 2101 个与塑料食品包装相关的化学特征,该数据库综合了三个来源的数据,其中 925 个特征是通过对八种常用塑料食品包装材料的化学提取物进行非目标筛选获得的。在这个数据库中,有 625 种化学特征,尤其是一半的非目标化学特征,是可能通过饮食摄入进入人体的潜在迁移物。对食品或人体血清样本中的塑料化学特征进行的生物监测分析表明,在 2101 个特征中,约 78% 可以检测到,约一半为非目标。其中,17 种在人体血清中检测频率较高的塑料化学物质被证实为功能性化学添加剂。总之,我们的工作表明,我们体内的塑料化学物质数量可能远远超过以前的认识,人类接触塑料化学物质可能对健康构成潜在风险。
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引用次数: 0
A new strategy integrating peroxymonosulfate oxidation and soil amendments in contaminated soil: Bensulfuron methyl degradation, soil quality improvement and maize growth promotion 将过硫酸盐氧化和土壤改良剂整合到受污染土壤中的新策略:苄嘧磺隆甲基降解、土壤质量改善和玉米生长促进
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135852
Xiaoyu Wang, Jiangyan Xu, Wei Chen, Ying Shi, Fang Liu, Hongmei Jiang

Bensulfuron methyl (BSM) residues have caused serious yield reductions of sensitive crops. Chemical oxidation is an effective remediation technology, while it affects soil quality and subsequent agricultural activity, necessitating approriate improvement measures. So Fe2O3-Mn3O4 with excellent bimetallic synergistic effect was synthesized to activate peroxymonosulfate (PMS) for BSM degradation. The catalytic activity and influencing factors were systematically predetermined in water in view of soil remediation. Results showed Fe2O3-Mn3O4/PMS oxidized 99.3 % BSM within 60 min with the help of multi-reactive species and electron transfer. Meanwhile, Fe2O3-Mn3O4/PMS treatment exhibited technical feasibility in soil that 97.6 % BSM was degraded in 5 days under the low usages of Fe2O3-Mn3O4 (0.8 %) and PMS (0.15 %). Although Fe2O3-Mn3O4/PMS decreased BSM phytotoxicity and improved maize growth, a few gaps existed between the remediated group and uncontaminated group, including biomass, length, available potassium, organic matters, pH, redox potential (Eh) and sulfate content. The introductions of biochar and chitosan in remediated soils promoted growth, increased organic matters content, improved soil resistance to acidification and decreased Eh, alleviating the negative effects of Fe2O3-Mn3O4/PMS. Overall, the study provided new insights into the combination of Fe2O3-Mn3O4/PMS and biochar and chitosan in BSM-contaminated soil, achieving BSM degradation and improvements of soil quality and plant growth.

苄嘧黄隆(BSM)残留物已导致敏感作物严重减产。化学氧化是一种有效的修复技术,但它会影响土壤质量和后续的农业活动,因此需要采取适当的改进措施。因此,研究人员合成了具有优异双金属协同效应的 Fe2O3-Mn3O4 来激活过一硫酸盐(PMS)降解 BSM。从土壤修复的角度出发,在水中系统地测定了催化活性和影响因素。结果表明,Fe2O3-Mn3O4/PMS 在多反应物和电子传递的帮助下,在 60 分钟内氧化了 99.3% 的 BSM。同时,Fe2O3-Mn3O4/PMS 处理在土壤中表现出技术可行性,在低用量 Fe2O3-Mn3O4(0.8%)和 PMS(0.15%)的情况下,5 天内 97.6% 的 BSM 被降解。虽然 Fe2O3-Mn3O4/PMS 降低了 BSM 的植物毒性并改善了玉米的生长,但在生物量、长度、可利用钾、有机物、pH 值、氧化还原电位(Eh)和硫酸盐含量等方面,修复组与未污染组之间仍存在一些差距。在修复土壤中引入生物炭和壳聚糖可促进生长、增加有机质含量、提高土壤抗酸化能力并降低 Eh,从而减轻 Fe2O3-Mn3O4/PMS 的负面影响。总之,该研究为在 BSM 污染土壤中将 Fe2O3-Mn3O4/PMS 与生物炭和壳聚糖相结合,实现 BSM 降解,改善土壤质量和植物生长提供了新的见解。
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引用次数: 0
Effect of phosphate-mineralized bacteria on multi-metals migration behavior in vanadium tailing slags: Coexistence of immobilization and mobilization 磷矿化细菌对钒尾渣中多金属迁移行为的影响:固定和移动的共存
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135880
Dinghua Peng , Yumei Zhang , Xianghan Chen , Ying Zhang , Huayan Huang , Huakang Liu , Heng Xu

Biomineralization techniques have been utilized to remediate heavy metals (HMs) contaminated environments. However, the effect of microbial-induced phosphate precipitation (MIPP) on HMs behavior in vanadium tailing slags has not been revealed. This study is the first to report the influence of MIPP on multiple HMs including Cd, Cu, Pb and Zn in the slags with and without soil mixing. The results showed that MIPP exhibited excellent ability for Cd immobilization, Cd immobilization rate reached 43.41 % under the optimal parameters within 7 days. Cd immobilization performance was significantly improved and sustained after the slags were covered with soil, resulting from better colonization of phosphate mineralizing bacteria in slag-soil mixtures. Surprisingly, DTPA-Cu, Zn and Pb contents in slags were all increased to varying degrees after MIPP treatment. Leaching solution mineralization tests further suggested that MIPP significantly reduced the concentration of Cd2+, Pb2+, Ca2+, Mg2+ and Al3+, but barely changed Cu2+ and Zn2+ concentrations. Characterization analysis confirmed that formation of phosphates including Cd(PO4)2 and dissolution of minerals including PbZnSiO2 were the reason for HMs immobilization and mobilization in vanadium tailing slags. This study provides new insights for understanding biomineralization technology and using MIPP to remediate HMs contaminated mine waste.

生物矿化技术已被用于修复重金属(HMs)污染的环境。然而,微生物诱导磷酸盐沉淀(MIPP)对钒尾渣中 HMs 行为的影响尚未被揭示。本研究首次报道了微生物诱导磷酸盐沉淀对钒尾渣中多种有害物质(包括镉、铜、铅和锌)的影响。结果表明,MIPP 对镉的固定化能力很强,在最佳参数下,7 天内镉的固定化率达到 43.41%。炉渣覆盖土壤后,镉的固定化性能得到明显改善和维持,这是因为磷酸盐矿化细菌在炉渣-土壤混合物中的定植效果更好。令人惊讶的是,经过 MIPP 处理后,炉渣中的 DTPA-铜、锌和铅含量都有不同程度的增加。浸出液矿化试验进一步表明,MIPP 能显著降低 Cd2+、Pb2+、Ca2+、Mg2+ 和 Al3+ 的浓度,但几乎没有改变 Cu2+ 和 Zn2+ 的浓度。表征分析证实,包括 Cd(PO4)2 在内的磷酸盐的形成和包括 PbZnSiO2 在内的矿物的溶解是 HMs 在钒尾渣中固定和移动的原因。这项研究为了解生物矿化技术和利用 MIPP 修复受 HMs 污染的矿山废料提供了新的见解。
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引用次数: 0
Methane oxidation coupling with heavy metal and microplastic transformations for biochar-mediated landfill cover soil 甲烷氧化与生物炭介导的垃圾填埋场覆盖土的重金属和微塑料转化耦合
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135879
Jiang Wu , Qiyong Xu , Rujie Zhang , Xinyue Bai , Chao Zhang , Qindong Chen , Huaihai Chen , Ning Wang , Dandan Huang

The impact of co-occurring heavy metal (HM) and microplastic (MP) pollution on methane (CH4) oxidation by methanotrophs (MOB) in landfill cover soil (LCS) and the role of biochar in mediating these collaborative transformations remains unclear. This study conducted batch-scale experiments using LCS treated with individual or combined HMs and MPs, with or without biochar amendment. Differentiation in methanotrophic activities, HM transformations, MP aging, soil properties, microbial communities, and functional genes across the groups were analyzed. Biochar proved essential in sustaining efficient CH4 oxidation under HM and MP stress, mainly by diversifying MOB, and enhancing polysaccharide secretion to mitigate environmental stress. While low levels of HMs slightly inhibited CH4 oxidation, high HM concentration enhanced methanotrophic activities by promoting electron transfer process. MPs consistently stimulated CH4 oxidation, exerting a stronger influence than HMs. Notably, the simultaneous presence of low levels of HMs and MPs synergistically boosted CH4 oxidation, linked to distinct microbial evolution and adaptation. Methanotrophic activities were demonstrated to affect the fate of HMs and MPs. Complete passivation of Cu was readily achieved, whereas Zn stabilization was negatively influenced by biochar and MPs. The aging of MPs was also partially suppressed by biochar and HM adsorption.

重金属(HM)和微塑料(MP)共存污染对垃圾填埋场覆盖土(LCS)中甲烷养分(MOB)氧化甲烷(CH4)的影响以及生物炭在介导这些协同转化中的作用仍不清楚。本研究使用单独或组合的 HMs 和 MPs 处理过的垃圾填埋场覆盖土(LCS)进行了批量实验,无论是否添加了生物炭。研究分析了各组甲烷营养体活性、甲烷转化、MP 老化、土壤性质、微生物群落和功能基因的差异。事实证明,在 HM 和 MP 胁迫下,生物炭对维持高效的 CH4 氧化至关重要,主要是通过使 MOB 多样化和增强多糖分泌来缓解环境胁迫。低浓度的 HMs 会轻微抑制 CH4 氧化,而高浓度的 HMs 则会通过促进电子传递过程来提高甲烷营养体的活性。MPs 始终刺激 CH4 氧化,其影响强于 HMs。值得注意的是,同时存在低浓度的 HMs 和 MPs 会协同促进 CH4 氧化,这与不同的微生物进化和适应有关。甲烷营养活动被证明会影响 HMs 和 MPs 的归宿。铜很容易完全钝化,而锌的稳定则受到生物炭和 MPs 的负面影响。生物炭和 HM 吸附也部分抑制了 MPs 的老化。
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引用次数: 0
Simultaneous removal of nutrients and pharmaceuticals and personal care products using two-stage woodchip bioreactor-biochar treatment systems 利用两级木屑生物反应器-生物炭处理系统同时去除营养物质、药物和个人护理产品
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135882
Hongxu Zhou , Haribansha Timalsina , Shuai Tang , Sophie Circenis , Jason Kandume , Richard Cooke , Buchun Si , Rabin Bhattarai , Wei Zheng

The co-occurrence of nutrients and pharmaceuticals and personal care products (PPCPs) in sewage effluent can degrade water quality of the receiving watersheds. This study investigated the simultaneous removal of excess nutrients and PPCP contaminants by developing a novel woodchip bioreactor and biochar (B2) treatment system. The result revealed that woodchip bioreactors could effectively remove nitrate via a denitrification process and adsorb some PPCPs. Biochar as a secondary treatment system significantly reduced the concentrations of PPCPs and dissolved reactive phosphorus (DRP) (p < 0.05), compared to the woodchip bioreactor. The removal efficiencies of all targeted contaminants by the B2 system were evaluated using various hydraulic retention times (HRTs) and biochar types (pelletized versus granular biochar). Longer HRTs and smaller biochar particles (granular biochar) could enhance the removal efficiencies of targeted contaminants. Average contaminant removals were 77.25 % for nitrate-N, 99.03 % for DRP, 69.51 % for ibuprofen, 73.65 % for naproxen, 91.09 % for sitagliptin, and 96.96 % for estrone, with woodchip bioreactor HRTs of 12 ± 1.4 h and granular biochar HRTs of 2.1 ± 0.1 h. Notably, the second-stage biochar systems effectively mitigated by-products leaching from woodchip bioreactors. The presence of PPCPs in the woodchip bioreactors enriched certain species, such as Methylophilus (69.6 %), while inhibiting other microorganisms and reducing microbial community diversity. Furthermore, a scaled-up B2 system was analyzed and assessed, indicating that the proposed engineering treatment system could provide decades of service in real-world applications. Overall, this study suggests that the B2 system has promising applications for addressing emerging and conventional contaminants.

污水中营养物质和药物及个人护理产品(PPCPs)的共存会使受纳流域的水质恶化。本研究通过开发新型木屑生物反应器和生物炭(B2)处理系统,对同时去除过量营养物和 PPCP 污染物进行了研究。结果表明,木屑生物反应器可通过反硝化过程有效去除硝酸盐,并吸附一些 PPCPs。与木屑生物反应器相比,生物炭作为二级处理系统可显著降低 PPCPs 和溶解性活性磷 (DRP) 的浓度(p < 0.05)。采用不同的水力停留时间(HRTs)和生物炭类型(颗粒状生物炭与粒状生物炭)对 B2 系统去除所有目标污染物的效率进行了评估。较长的水力停留时间和较小的生物炭颗粒(颗粒状生物炭)可提高目标污染物的去除率。木片生物反应器的 HRT 为 12 ± 1.4 小时,颗粒生物炭的 HRT 为 2.1 ± 0.1 小时,污染物的平均去除率分别为硝酸盐-N(77.25%)、DRP(99.03%)、布洛芬(69.51%)、萘普生(73.65%)、西他列汀(91.09%)和雌酮(96.96%)。值得注意的是,第二阶段生物炭系统有效地减轻了木片生物反应器中副产品的沥滤。木片生物反应器中 PPCPs 的存在富集了某些物种,例如嗜甲菌(69.6%),同时抑制了其他微生物,降低了微生物群落的多样性。此外,还对一个扩大的 B2 系统进行了分析和评估,表明拟议的工程处理系统可在实际应用中提供数十年的服务。总之,这项研究表明,B2 系统在处理新兴和传统污染物方面具有广阔的应用前景。
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引用次数: 0
Flumethrin exposure perturbs gut microbiota structure and intestinal metabolism in honeybees (Apis mellifera) 接触氟氯氰菊酯会扰乱蜜蜂(Apis mellifera)肠道微生物群结构和肠道新陈代谢
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135886
Jianhui Liu , Jingliang Shi , Yueyang Hu , Yuchen Su , Yonghong Zhang , Xiaobo Wu

Flumethrin mitigates Varroa’s harm to honeybee colonies; however, its residues in colonies threaten the fitness of honeybee hosts and gut microbiota. Our previous research has shown that flumethrin induces significant physiological effects on honeybee larvae; but the effects of flumethrin on the gut microbiota and metabolism of adult honeybees are still unknown. In this study, 1-day-old honeybees were exposed to 0, 0.01, 0.1, and 1 mg/L flumethrin for 14 days and the impacts of flumethrin on the intestinal system were evaluated. The results showed that exposure to 1 mg/L flumethrin significantly reduced honeybee survival and the activities of antioxidative enzymes (superoxide dismutase and catalase) and detoxification enzymes (glutathione S-transferase) in honeybee heads. Moreover, exposure to 0.01, 0.1, and 1 mg/L flumethrin significantly decreased the diversity of the honeybee gut microbiota. Results from untargeted metabolomics showed that long-term exposure to 0.01, 0.1, and 1 mg/L flumethrin caused changes in the metabolic pathways of honeybee gut microbes. Furthermore, increased metabolism of phenylalanine, tyrosine, and tryptophan derivatives was observed in honeybee gut microbes. These findings underscore the importance of careful consideration in using pesticides in apiculture and provide a basis for safeguarding honeybees from pollutants, considering the effects on gut microbes.

氟氯氰菊酯可减轻 Varroa 对蜜蜂蜂群的危害,但其在蜂群中的残留物会威胁蜜蜂宿主和肠道微生物群的健康。我们之前的研究表明,氟氯氰菊酯会对蜜蜂幼虫产生显著的生理影响;但氟氯氰菊酯对成年蜜蜂肠道微生物群和新陈代谢的影响尚不清楚。本研究将 1 日龄蜜蜂分别暴露于 0、0.01、0.1 和 1 mg/L 氟氯氰菊酯 14 天,并评估了氟氯氰菊酯对肠道系统的影响。结果表明,接触 1 毫克/升氟氯氰菊酯会显著降低蜜蜂的存活率以及蜜蜂头部抗氧化酶(超氧化物歧化酶和过氧化氢酶)和解毒酶(谷胱甘肽 S-转移酶)的活性。此外,接触 0.01、0.1 和 1 mg/L 氟氯氰菊酯会显著降低蜜蜂肠道微生物群的多样性。非靶向代谢组学研究结果表明,长期接触 0.01、0.1 和 1 mg/L 氟氯氰菊酯会导致蜜蜂肠道微生物的代谢途径发生变化。此外,在蜜蜂肠道微生物中观察到苯丙氨酸、酪氨酸和色氨酸衍生物的代谢增加。这些发现强调了在养蜂业中使用杀虫剂时慎重考虑的重要性,并为保护蜜蜂免受污染物影响提供了依据,同时考虑到了对肠道微生物的影响。
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引用次数: 0
Evidence that beneficial microbial inoculation enhances heavy metal-contaminated soil remediation: Variations in plant endophyte communities 有益微生物接种可加强重金属污染土壤修复的证据:植物内生菌群落的变化
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135883
Fangming Yu , Ziang He , Xiaomin Xin , Xinwei Shi , Lixing Chen , Xinying He , Yueying Huang , Yi Li

Microbial remediation of heavy metal (HM)-contaminated soil is a sustainable approach; however, the impact of microbial inoculation on the internal environment of plants remains understudied. Thus, Enterobacter sp. FM-1 (Enterobacter sp.) and the hyperaccumulator Bidens pilosa L. (B. pilosa L.) were used to study these effects. Through analyses of plant physiological and biochemical characteristics, the endophytic microbial community composition, microbial co-occurrence networks and functional predictions, the potential mechanisms by which Enterobacter sp. benefits the phytoremediation of HM-contaminated soil by B. pilosa L. were elucidated. Inoculation with Enterobacter sp. promoted the growth of B. pilosa L. and influenced the endophytic microbial community diversity in B. pilosa L. Interactions among endophytes facilitated the formation of microbial networks, with endophytic fungi playing a more prominent role than endophytic bacteria as the level of HM contamination increased. Functional predictions via PICRUSt2 revealed that endophytic bacteria are involved primarily in processes related to carbohydrate metabolism, ABC transporters, and amino acid metabolism. In conclusion, this study provides evidence for the beneficial role of microbes in improving the plant endosphere environment.

对重金属(HM)污染的土壤进行微生物修复是一种可持续的方法;然而,微生物接种对植物内部环境的影响仍未得到充分研究。因此,我们使用肠杆菌 FM-1 和高积累菌 Bidens pilosa L. (B. pilosa L.)来研究这些影响。通过对植物生理生化特征、内生微生物群落组成、微生物共生网络和功能预测的分析,阐明了肠杆菌有利于 B. pilosa L. 对受 HM 污染的土壤进行植物修复的潜在机制。内生菌之间的相互作用促进了微生物网络的形成,随着 HM 污染程度的增加,内生真菌的作用比内生细菌更为突出。通过 PICRUSt2 进行的功能预测显示,内生细菌主要参与碳水化合物代谢、ABC 转运体和氨基酸代谢的相关过程。总之,这项研究为微生物在改善植物内圈环境中的有益作用提供了证据。
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引用次数: 0
Interplay of humic acid and Cr(VI) on green microalgae: Metabolic responses and chromium enrichment 腐殖酸和六价铬对绿色微藻的相互作用:代谢反应和铬富集
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135885
Li Luo , Tong Yang , Mawuli Dzakpasu , Xu Jiang , Wenshan Guo , Huu Hao Ngo , Xiaochang C. Wang

Dissolved organic matter (DOM) present in aquatic environments can significantly influence microalgal metabolism and the enrichment of heavy metals. However, the specific mechanism through which typical DOM affects the enrichment of the heavy metal chromium (Cr) in green algae remains unclear. This study investigates the impacts of varying concentrations of humic acid (HA), selected as a representative DOM in water, on the growth, metabolism, and Cr enrichment in Chlorella vulgaris, a typical green alga. The results indicated that low concentrations of HA were capable of enhancing Cr enrichment in C. vulgaris, with the highest Cr enrichment rate recorded at 41.50 % at TOC = 10 mg/L. The enrichment of Cr in algal cells primarily occurred through cell proliferation and complexation reduction of extracellular polymeric substances (EPS). In the presence of HA, C. vulgaris predominantly removed Cr through extracellular adsorption, accounting for 79.76–85.88 % of the total Cr removal. Furthermore, carboxyl complexation and hydroxyl reduction within EPS facilitated both the enrichment of Cr (18.72–21.49 %) and the reduction of Cr(VI) (63.93–74.10 %). These findings provide valuable insights into strategies for mitigating heavy metal pollution and managing associated risks in aquatic environments.

水生环境中的溶解有机物(DOM)会对微藻的新陈代谢和重金属富集产生重大影响。然而,典型 DOM 影响重金属铬(Cr)在绿藻中富集的具体机制仍不清楚。本研究调查了不同浓度的腐植酸(HA)对典型绿藻绿球藻(Chlorella vulgaris)的生长、代谢和铬富集的影响。结果表明,低浓度的 HA 能够提高绿藻中铬的富集率,当 TOC = 10 mg/L 时,绿藻中铬的富集率最高,达到 41.50%。铬在藻类细胞中的富集主要是通过细胞增殖和胞外聚合物质(EPS)的复合减少实现的。在有 HA 存在的情况下,褐藻主要通过胞外吸附去除铬,占铬去除总量的 79.76-85.88%。此外,EPS 中的羧基络合和羟基还原促进了铬的富集(18.72-21.49%)和六价铬的还原(63.93-74.10%)。这些发现为减轻重金属污染和管理水生环境中相关风险的策略提供了宝贵的见解。
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引用次数: 0
A novel sequential extraction method for the measurement of Cr(VI) and Cr(III) species distribution in soil: New insights into the chromium speciation 测量土壤中六价铬和三价铬物种分布的新型顺序萃取法:铬标示的新见解
IF 12.2 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Pub Date : 2024-09-17 DOI: 10.1016/j.jhazmat.2024.135864
Qian Guo , Dongmei Yu , Jing Yang , Ting Zhao , Dan Yu , Lei Li , Duanjie Wang

The distribution characteristics of Cr(VI) species in contaminated soil is crucial for soil remediation; however, there is currently a lack of methods for analysing anionic Cr(VI) species in soil. This study has developed a novel sequential extraction method for speciation of Cr(VI) and Cr(III). Besides extraction experiments, simulated chromium species were prepared to verify the presence of proposed chromium species. The results show that Cr(VI) species in soil can be categorized into water-soluble Cr(VI), electrostatically adsorbed Cr(VI), Cr(VI) specifically adsorbed by minerals containing exchangeable Ca2+, Cr(VI) specifically adsorbed by hydrous metal oxides, calcium chromate Cr(VI) and stable complexed adsorption Cr(VI). These Cr(VI) species can be selectively extracted by specific solutions through ion exchange or weak acid dissolution. The most stable Cr(VI) species is Cr(VI) complexed by hydrous iron oxides through bidentate ligand binding; only by dissolution of hydrous iron oxides can this Cr(VI) species be leached. The distribution of Cr(VI) species is closely linked to particular soil compositions including exchangeable Ca2+ and hydrous iron oxides which determinate the Cr(VI) adsorption in soil. Cr(III) species comprise Fe-Cr coprecipitate hydroxides Cr(III), Fe-Mn oxide-bound Cr(III), organic matter-bound Cr(III) and residual Cr(III). Their distribution depends on the types of reductants present in the soil.

六价铬在受污染土壤中的分布特征对于土壤修复至关重要;然而,目前缺乏分析土壤中阴离子六价铬的方法。本研究开发了一种新型的顺序萃取法,用于六价铬和三价铬的标样分析。除萃取实验外,还制备了模拟铬物种,以验证拟议铬物种的存在。结果表明,土壤中的六价铬可分为水溶性六价铬、静电吸附六价铬、含可交换 Ca2+ 的矿物特异性吸附六价铬、水合金属氧化物特异性吸附六价铬、铬酸钙六价铬和稳定的络合吸附六价铬。这些六价铬物种可以通过离子交换或弱酸溶解的方式被特定溶液选择性地提取出来。最稳定的六价铬是通过双齿配体结合与水合氧化铁络合的六价铬,只有溶解水合氧化铁才能萃取这种六价铬。六价铬的分布与特定的土壤成分密切相关,包括可交换的 Ca2+ 和水合氧化铁,它们决定了六价铬在土壤中的吸附性。铬(III)的种类包括铁-铬共沉淀氢氧化物铬(III)、铁-锰氧化物结合铬(III)、有机物结合铬(III)和残留铬(III)。它们的分布取决于土壤中还原剂的类型。
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引用次数: 0
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Journal of Hazardous Materials
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