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Presence and sources of per- and polyfluoroalkyl substances (PFASs) in the three major rivers on Hainan Island. 海南岛三条主要河流中全氟烷基和多氟烷基物质(PFASs)的存在及来源
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-14 DOI: 10.1016/j.envres.2024.120590
Wang-Qing Tang, Tuan-Tuan Wang, Jiang-Wei Miao, Hua-Dong Tan, Hong-Jin Zhang, Tuan-Qi Guo, Zhong-Bing Chen, Chun-Yuan Wu, Ling Mo, Bi-Xian Mai, Sai Wang

Per- and polyfluoroalkyl substances (PFASs) have attracted considerable attention because of their toxicity, persistence and bioaccumulation potential. With the construction of the Hainan Free Trade Port and the rapid development of economy, environmental pollution on Hainan Island is becoming increasingly prominent. PFASs have been detected in the seawater and sediments of mangrove ecosystems on Hainan Island. As the receiving water of wastewater treatment plants (WWTPs) and industrial wastewater, rivers are inevitably contaminated by PFASs. However, few studies have focused on PFAS pollution in three large rivers (the Nandu, Changhua, and Wanquan rivers) on Hainan Island. In the present study, the pollution status, potential sources, and ecological risks of PFASs in these three major rivers were explored. Perfluorobutanonic acid (PFBA) (48.7%) was found to be the major PFASs in the surface waters, and perfluoroundecanoic acid (PFUnDA) (19.7%) was the major PFASs in the sediments of the three major rivers. The concentrations of ∑PFASs in the upper-midstream region were low due to minimal human influence and increased in the middle-lower reaches with increasing industrial activity and urbanization, whereas decreased at downstream sites near estuaries where river water was diluted with seawater. WWTP effluent, industrial wastewater discharge, the application and discharge of aqueous fire-fighting foam, storm runoff and landfill leachate were the major sources of PFASs in the three major rivers. In surface water, perfluorooctanoic acid (PFOA), perfluorooctane sulfonamide (PFOSA) and perfluorooctadecanoic acid (PFODA) posed low-moderate risks at 5.71-85.6% of the sampling sites. PFASs in the sediment posed no ecological risk. This study provides key data regarding the pollution status and potential sources of PFASs in large rivers on subtropical islands.

全氟和多氟烷基物质(PFASs)因其毒性、持久性和生物蓄积性而受到广泛关注。随着海南自由贸易港的建设和经济的快速发展,海南岛的环境污染问题日益突出。在海南岛红树林生态系统的海水和沉积物中检测到PFASs。河流作为污水处理厂和工业废水的接收水,不可避免地受到PFASs的污染。然而,对海南岛南渡河、彰化河和万泉河三大河流PFAS污染的研究较少。本研究对这三条主要河流的全氟辛烷污染现状、潜在来源和生态风险进行了探讨。地表水中全氟丁酸(PFBA)占48.7%,三条主要河流沉积物中全氟癸酸(PFUnDA)占19.7%。∑PFASs在中上游地区受人为影响较小,浓度较低,随着工业活动和城市化的增加,中下游地区浓度升高,而在靠近河口的下游地区,由于河水被海水稀释,∑PFASs浓度降低。污水处理厂出水、工业废水排放、消防泡沫水的应用和排放、暴雨径流和垃圾渗滤液是三大河流中PFASs的主要来源。在地表水中,全氟辛酸(PFOA)、全氟辛烷磺酰胺(PFOSA)和全氟十六烷酸(PFODA)在5.71-85.6%的采样点构成中低风险。沉积物中全氟辛烷不构成生态风险。本研究为研究亚热带海岛大型河流中全氟辛烷磺酸的污染现状和潜在来源提供了关键数据。
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引用次数: 0
Individual and joint associations of exposure to per- and polyfluoroalkyl substances with children's mitochondrial DNA copy number, and modified by estimated glomerular filtration rate. 暴露于全氟烷基和多氟烷基物质与儿童线粒体DNA拷贝数的个体和联合关联,并通过估计的肾小球滤过率加以修正。
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-10 DOI: 10.1016/j.envres.2024.120598
Biao Zhang, Jie Wang, Yuanyuan Zhang, Miao Liu, Xiaomin Zhang

Background: The association between per- and polyfluoroalkyl substances (PFAS) and mitochondrial DNA copy number (mtDNAcn) in children, and the potential impact of estimated glomerular filtration rate (eGFR) on this association, remains unclear.

Methods: We conducted a panel study with up to 3 surveys over 3 seasons in Weinan and Guangzhou, China. A total of 284 children aged 4-12 years were available, with 742 measurements of 11 PFAS and mtDNAcn. Linear mixed-effect (LME), quantile g-computation (qgcomp), weighted quantile sum (WQS) regression, and Bayesian kernel machine regression (BKMR) models were used to investigate the associations of individuals and a mixture of PFAS with mtDNAcn, and the modifying effect of eGFR on these associations.

Results: Legacy PFAS, including perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUnDA), perfluorooctane sulfonate (PFOS) and emerging PFAS, 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFESA), were significantly associated with decreased mtDNAcn in a linear dose-response manner (FDR <0.05). The multiple PFAS model showed each doubling increase in PFOA related to a 6.36% (95%CI: -10.22%, -2.34%) decrement in mtDNAcn. Meanwhile, the PFAS mixture was dose-responsive related to decreased mtDNAcn, with PFOA being the largest contributor, followed by PFUnDA and PFNA. Notably, eGFR modified the inverse association between PFOA and mtDNAcn (P-int = 0.039), with a more pronounced decrement in children with an eGFR below the 20th value (101.71 mL/min/1.73m2). In addition, age significantly modified the relationship between PFOA and decreased mtDNAcn (P-int = 0.028), with a stronger association in those aged 7 years or older.

Conclusion: Both individual and the mixture of legacy and emerging PFAS exposure were associated with decreased mtDNAcn in children, with PFOA as the main contributor and modification of eGFR.

背景:全氟烷基和多氟烷基物质(PFAS)与儿童线粒体DNA拷贝数(mtDNAcn)之间的关系,以及估计的肾小球滤过率(eGFR)对这种关系的潜在影响尚不清楚。方法:我们在中国渭南和广州进行了一项为期3个季节的小组研究。共有284名4至12岁的儿童,进行了11项PFAS和mtDNAcn的742次测量。采用线性混合效应(LME)、分位数g计算(qgcomp)、加权分位数和(WQS)回归和贝叶斯核机回归(BKMR)模型研究个体与PFAS与mtDNAcn混合的关联,以及eGFR对这些关联的调节作用。传统PFAS,包括全氟辛酸(PFOA)、全氟壬酸(PFNA)、全氟癸酸(PFDA)、全氟癸酸(PFUnDA)、全氟辛烷磺酸(PFOS)和新出现的PFAS、6:2氯化多氟醚磺酸(6:2 Cl-PFESA),与mtDNAcn的降低呈线性剂量-反应关系(FDR < 0.05)。多重PFAS模型显示,PFOA每增加一倍,mtDNAcn减少6.36% (95%CI: -10.22%, -2.34%)。同时,PFAS混合物与mtDNAcn的降低呈剂量响应关系,其中PFOA是最大的贡献者,其次是PFUnDA和PFNA。值得注意的是,eGFR改变了PFOA和mtDNAcn之间的负相关关系(P-int = 0.039),在eGFR低于20值(101.71 mL/min/1.73m2)的儿童中下降更为明显。此外,年龄显著改变了PFOA与mtDNAcn下降的关系(P-int=0.028),其中7岁及以上的相关性更强。结论:儿童mtDNAcn的降低与个体暴露以及遗留和新出现的PFAS暴露的混合暴露有关,其中PFOA是eGFR的主要贡献者和改变因素。
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引用次数: 0
Quorum quenching inhibits the formation and electroactivity of electrogenic biofilm by weakening intracellular c-di-GMP and extracellular AHL-mediated signal communication. 群体猝灭通过削弱细胞内c-di-GMP和细胞外ahl介导的信号通信来抑制电致生物膜的形成和电活性。
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-10 DOI: 10.1016/j.envres.2024.120604
Qian Zhu, Yingying Du, Yanyan Zheng, Ziyi Hu, Zikang Liu, Jingping Hu, Huijie Hou

Electrogenic biofilm formation has been shown to be induced by intracellular c-di-GMP signaling and extracellular quorum sensing, but their interactions have been rarely explored. This study explored the effects of quorum quenching (induced by adding acylase) on electrogenic biofilm development and its underlying mechanisms. Quorum quenching impaired the electricity generation and electroactivity of electrogenic biofilms as indicated by dye decolorization rate. It significantly decreased the proportion of typical exoelectrogen Geobacter from 62.0% to 36.5% after 90 days of operation, and enriched some other functional genera (e.g., Dysgonomonas and Sphaerochaeta) to ensure normal physiological function. Moreover, metagenomic analysis revealed that the addition of acylase weakened the potential of chemical communication, as indicated by the decrease in the abundance of genes encoding the production of AHL and c-di-GMP, and the increase in the abundance of aiiA and pvdQ genes (encoding quorum quenching) and cdgC gene (responsible for c-di-GMP breakdown). Functional contribution analysis indicated that Geobacter was a major contributor to hdtS gene (encoding AHL synthesis). These findings demonstrated that quorum quenching adversely impaired not only quorum sensing but also intracellular c-di-GMP signaling, ultimately inhibiting the development of biofilm. This work lays the foundation for regulating electrogenic biofilm development and improving the performance of microbial electrochemical system using signal communication strategy.

电致生物膜的形成被证明是由细胞内c-di-GMP信号和细胞外群体感应诱导的,但它们之间的相互作用很少被探索。本研究探讨了添加酰基酶诱导的群体猝灭对电生生物膜发育的影响及其机制。从染料脱色率可以看出,群体猝灭破坏了电生生物膜的发电和电活性。运行90 d后,显著降低了典型外电地杆菌的比例,由62.0%降至36.5%,并丰富了其他一些功能属(如Dysgonomonas和Sphaerochaeta),保证了正常的生理功能。此外,宏基因组分析显示,乙酰化酶的加入削弱了化学通讯的潜力,这表明编码AHL和c-di-GMP的基因丰度降低,编码群体猝灭的aiiA和pvdQ基因以及负责c-di-GMP分解的cdgC基因的丰度增加。功能贡献分析表明,Geobacter是hdtS基因(编码AHL合成)的主要贡献者。这些发现表明,群体猝灭不仅会损害群体感应,还会损害细胞内c-di-GMP信号,最终抑制生物膜的发育。该工作为利用信号通信策略调控电生生物膜的发育和提高微生物电化学系统的性能奠定了基础。
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引用次数: 0
Elucidating the role of the genus Pseudomonas involved in coumarin degradation. 阐明假单胞菌在香豆素降解中的作用。
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-10 DOI: 10.1016/j.envres.2024.120603
Shunli Hu, Peicheng Lu, Youhui Feng, Anqi Chen, Guomin Han

Coumarin, a synthetic chemical and phytotoxin, exhibits hepatotoxicity and carcinogenicity, posing threats to both human health and environmental safety. Microbial degradation effectively mitigates environmental contamination. In this study, a coumarin-degrading bacterial consortium designated as XDS-7 with Pseudomonas as the key degrader was obtained. However, there is a lack of comprehensive perspective on the key role of the genus Pseudomonas involved in coumarin degradation. We employed the consortium XDS-7 as a model system to investigate the critical role of the genus Pseudomonas involved in coumarin degradation. Metagenomic binning analysis indicated that bin 14 (Pseudomonas sp.) contains the full complement of genes required for coumarin degradation. A coumarin-degrading bacterium, Pseudomonas sp. strain X4, was isolated from consortium XDS-7 using a traditional enrichment method supplemented with chloramphenicol. Genomic analysis demonstrated that strain X4 carries a suite of genes to completely degrade coumarin. Bioinformatics analysis revealed that putative coumarin-degrading bacteria are widely distributed across diverse bacteria of the genus Pseudomonas. In addition, strain X4 completely removed 100 mg kg-1 of coumarin from contaminated soil within 48 h and 100 mg L-1 of coumarin from contaminated wastewater within 4 h. This study will greatly enhance our understanding and utilization of these valuable bioresources.

香豆素是一种合成化学物质和植物毒素,具有肝毒性和致癌性,对人类健康和环境安全构成威胁。微生物降解有效地减轻了环境污染。本研究获得了以假单胞菌为主要降解菌的香豆素降解菌群XDS-7。然而,对假单胞菌属在香豆素降解中的关键作用缺乏全面的认识。我们采用XDS-7作为模型系统来研究假单胞菌属在香豆素降解中的关键作用。宏基因组分析表明,bin 14 (Pseudomonas sp.)含有香豆素降解所需的全部基因。采用传统富集方法,在菌株XDS-7中添加氯霉素,分离得到一株香豆素降解菌X4。基因组分析表明,菌株X4携带一套完全降解香豆素的基因。生物信息学分析表明,假定的香豆素降解细菌广泛分布于假单胞菌属的各种细菌中。此外,菌株X4在48 h内完全脱除了污染土壤中的100 mg kg-1香豆素,在4 h内完全脱除了污染废水中的100 mg L-1香豆素。该研究将大大提高我们对这些宝贵生物资源的认识和利用。
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引用次数: 0
Activated CdS/ sulfur doped g-C3N4 photocatalyst for dye and antibiotic degradation: Experimental and DFT verification of S-scheme heterojunction. 活化CdS/硫掺杂g-C3N4光催化剂用于染料和抗生素降解:s -图式异质结的实验和DFT验证。
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-11-29 DOI: 10.1016/j.envres.2024.120487
Xu Duan, Jian Yang, Jiaqing Zhu, Hongbin Li, Yujie Fang, Runxue Liu, Chen Yang, Weizao Liu, Chunlian Ding, Qingcai Liu, Jiangling Li, Shan Ren

To alleviate situation caused by azo dyestuff and antibiotics, a series of CdS/sulfur doped carbon nitride (GCNS) S-scheme heterojunction photocatalysts have been successfully fabricated by a pretty facile solid-state diffusion (SSD) method,. Under visible light, the optimal sample called CdS/GCNS-1:2 presented the best photodegradation rate of nearly 100% over methyl orange (MO), of which the reaction constant k was about 9.67 and 5.39 times higher than that of pure GCNS and CdS, respectively. Degradation rate of 91% over tetracycline hydrochloride (TCH) was achieved within 60 min as well. The DFT calculations, XPS and charge flow tracking tests clarified the surge of C-S linkages and the construction of interfacial S-scheme heterojunction. The former promoted the fixation and conversion of adsorbed oxygen, while the latter accelerated the separation/transport of charge carriers. These tuning eventually collaborates on the promotion of •O2- reactive species, which confirmed as the predominant role of photoreaction. Furthermore, the plausible degradation pathways of MO/TCH and photocatalytic optimization mechanism were thoroughly elucidated.

为了减轻偶氮染料和抗生素的影响,采用一种简单的固态扩散(SSD)方法成功制备了一系列CdS/硫掺杂氮化碳(GCNS) s型异质结光催化剂。在可见光下,最优样品CdS/GCNS-1:2对甲基橙(MO)的光降解率接近100%,其反应常数k分别比纯GCNS和CdS高9.67倍和5.39倍。60 min内对盐酸四环素(TCH)的降解率为91%。DFT计算、XPS和电荷流跟踪实验明确了C-S键的涌动和界面s型异质结的构建。前者促进了吸附氧的固定和转化,后者则加速了载流子的分离/输运。这些调整最终协同促进•O2-反应物质,这证实了光反应的主要作用。进一步深入探讨了MO/TCH的降解途径及光催化优化机理。
{"title":"Activated CdS/ sulfur doped g-C<sub>3</sub>N<sub>4</sub> photocatalyst for dye and antibiotic degradation: Experimental and DFT verification of S-scheme heterojunction.","authors":"Xu Duan, Jian Yang, Jiaqing Zhu, Hongbin Li, Yujie Fang, Runxue Liu, Chen Yang, Weizao Liu, Chunlian Ding, Qingcai Liu, Jiangling Li, Shan Ren","doi":"10.1016/j.envres.2024.120487","DOIUrl":"10.1016/j.envres.2024.120487","url":null,"abstract":"<p><p>To alleviate situation caused by azo dyestuff and antibiotics, a series of CdS/sulfur doped carbon nitride (GCNS) S-scheme heterojunction photocatalysts have been successfully fabricated by a pretty facile solid-state diffusion (SSD) method,. Under visible light, the optimal sample called CdS/GCNS-1:2 presented the best photodegradation rate of nearly 100% over methyl orange (MO), of which the reaction constant k was about 9.67 and 5.39 times higher than that of pure GCNS and CdS, respectively. Degradation rate of 91% over tetracycline hydrochloride (TCH) was achieved within 60 min as well. The DFT calculations, XPS and charge flow tracking tests clarified the surge of C-S linkages and the construction of interfacial S-scheme heterojunction. The former promoted the fixation and conversion of adsorbed oxygen, while the latter accelerated the separation/transport of charge carriers. These tuning eventually collaborates on the promotion of •O<sub>2</sub><sup>-</sup> reactive species, which confirmed as the predominant role of photoreaction. Furthermore, the plausible degradation pathways of MO/TCH and photocatalytic optimization mechanism were thoroughly elucidated.</p>","PeriodicalId":312,"journal":{"name":"Environmental Research","volume":" ","pages":"120487"},"PeriodicalIF":7.7,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142765143","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Per- and polyfluoroalkyl substances (PFAS) accumulation in fish occupying different trophic positions from East Canyon Creek, a seasonally effluent-dominated river, Utah, USA. 东峡谷溪是美国犹他州一条季节性污水为主的河流,其不同营养位置的鱼类中全氟和多氟烷基物质(PFAS)的积累
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-11-28 DOI: 10.1016/j.envres.2024.120480
Yelena Sapozhnikova, Kevin M Stroski, Samuel P Haddad, S Rebekah Burket, Michael Luers, Bryan W Brooks

Fish and seafood are considered a major source of human dietary exposure to per- and polyfluoroalkyl substances (PFAS). In this study, we examined levels of 35 PFAS in fish samples of brown trout and mottled sculpin, which occupy different trophic positions, collected in 2014 from East Canyon Creek in Utah, USA. We observed 20 PFAS with ∑20PFAS ranging from 0.46-63.9 ng/g and from

鱼类和海产品被认为是人类从饮食中接触全氟烷基和多氟烷基物质的主要来源。在这项研究中,我们检测了2014年在美国犹他州东峡谷溪采集的处于不同营养位置的褐鳟鱼和斑驳鱼样本中35种PFAS的水平。共观察到20个PFAS,∑20PFAS范围为0.46 ~ 63.9 ng/g
{"title":"Per- and polyfluoroalkyl substances (PFAS) accumulation in fish occupying different trophic positions from East Canyon Creek, a seasonally effluent-dominated river, Utah, USA.","authors":"Yelena Sapozhnikova, Kevin M Stroski, Samuel P Haddad, S Rebekah Burket, Michael Luers, Bryan W Brooks","doi":"10.1016/j.envres.2024.120480","DOIUrl":"10.1016/j.envres.2024.120480","url":null,"abstract":"<p><p>Fish and seafood are considered a major source of human dietary exposure to per- and polyfluoroalkyl substances (PFAS). In this study, we examined levels of 35 PFAS in fish samples of brown trout and mottled sculpin, which occupy different trophic positions, collected in 2014 from East Canyon Creek in Utah, USA. We observed 20 PFAS with ∑<sub>20</sub>PFAS ranging from 0.46-63.9 ng/g and from <LOQ-52.1 ng/g wet weight in sculpin and brown trout, respectively. Among detected compounds, PFOS was measured at highest levels ranging 3.8-46.5 ng/g in sculpin, which occupies a lower trophic level, and 2.5-38.4 ng/g in brown trout, which occupies a higher trophic position. The most frequently detected PFAS were PFDA and FOSA, and these contaminants were found in 93% and 81% of fish samples; however, we did not identify appreciable PFAS biomagnification. To evaluate potential risk associated with consumption of fish, we calculated risk-based consumption limits using European Food Safety Authority (EFSA) regulated values of maximum levels (MLs) and total weekly intake for four regulated PFAS: PFOA, PFNA, PFHxS, and PFOS. The levels of regulated PFAS exceeded at least one of the MLs in 74% of sculpin samples and 45% of brown trout samples. Based on calculated weekly intake for the sum of the four regulated PFAS, a typical adult would need to consume 4.2 and 5.6 meals per week of whole body sculpin and brown trout, respectively, to reach the tolerable weekly intake (TWI) of 4.4 ng/kg body weight per week set by EFSA.</p>","PeriodicalId":312,"journal":{"name":"Environmental Research","volume":" ","pages":"120480"},"PeriodicalIF":7.7,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142754405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficient removal and recovery of phosphate by biochar loaded with ultrafine MgO nanoparticles. 负载超细MgO纳米颗粒的生物炭对磷酸盐的高效去除和回收。
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-07 DOI: 10.1016/j.envres.2024.120518
Yanpeng Huang, Qiong Wu, Jingfan Yan, Fumin Chu, Yuming Xu, Dongmin Li, Hongjia Zhang, Sen Yang

Biochar loaded with MgO is a promising adsorbent for the removal and recovery of phosphate from aqueous solutions. However, its phosphate adsorption capacity is unsatisfactory, especially at low phosphate concentrations. Loading nanoscale MgO onto biochar is an effective strategy. Here, ultrafine MgO nanoparticles and MgO nanosheets were loaded onto biochar from steam-exploded straw (UMB and SMB) via an impregnation-precipitation-pyrolysis method. The crystal sizes of ultrafine MgO nanoparticles and MgO nanosheets were about 6-8 nm and 10-16 nm, respectively. The phosphate adsorption capacity of UMB at C0 = 100 mg P L-1 was 219.4 mg P g-1, which was higher than that of SMB (164.9 mg P g-1). The results suggest that surface precipitation was the dominant adsorption mechanism and the hydration process and the smaller particle size of MgO may play a key role in the superior phosphate removal by UMB. Removal tests in real low-concentration phosphate water samples showed that 0.05 g L-1 UMB could reduce the phosphate concentration from 0.17 mg P L-1 to 0.01 mg P L-1. In addition, phosphate could be desorbed from UMB in varying environments, and therefore has the potential to be used in fertilizer production or directly as a slow-release fertilizer.

负载MgO的生物炭是一种很有前途的吸附剂,用于从水溶液中去除和回收磷酸盐。然而,其对磷酸盐的吸附能力并不理想,特别是在低磷酸盐浓度下。将纳米级MgO装载到生物炭上是一种有效的策略。通过浸渍-沉淀-热解的方法,将超细MgO纳米颗粒和MgO纳米片加载到蒸汽爆炸秸秆(UMB和SMB)的生物炭上。超细MgO纳米颗粒和MgO纳米片的晶粒尺寸分别约为6 ~ 8 nm和10 ~ 16 nm。在C0=100 mg P -1时,UMB对磷酸盐的吸附量为219.4 mg P -1,高于SMB (164.9 mg P -1)。结果表明,表面沉淀是主要的吸附机制,水化过程和较小的MgO粒径可能是UMB高效除磷的关键因素。对实际低浓度磷酸盐水样的去除试验表明,0.05 g L-1 UMB可将磷酸盐浓度从0.17 mg P -1降至0.01 mg P -1。此外,磷酸盐可以在不同的环境下从UMB中解吸,因此有潜力用于肥料生产或直接作为缓释肥料。
{"title":"Efficient removal and recovery of phosphate by biochar loaded with ultrafine MgO nanoparticles.","authors":"Yanpeng Huang, Qiong Wu, Jingfan Yan, Fumin Chu, Yuming Xu, Dongmin Li, Hongjia Zhang, Sen Yang","doi":"10.1016/j.envres.2024.120518","DOIUrl":"10.1016/j.envres.2024.120518","url":null,"abstract":"<p><p>Biochar loaded with MgO is a promising adsorbent for the removal and recovery of phosphate from aqueous solutions. However, its phosphate adsorption capacity is unsatisfactory, especially at low phosphate concentrations. Loading nanoscale MgO onto biochar is an effective strategy. Here, ultrafine MgO nanoparticles and MgO nanosheets were loaded onto biochar from steam-exploded straw (UMB and SMB) via an impregnation-precipitation-pyrolysis method. The crystal sizes of ultrafine MgO nanoparticles and MgO nanosheets were about 6-8 nm and 10-16 nm, respectively. The phosphate adsorption capacity of UMB at C<sub>0</sub> = 100 mg P L<sup>-1</sup> was 219.4 mg P g<sup>-1</sup>, which was higher than that of SMB (164.9 mg P g<sup>-1</sup>). The results suggest that surface precipitation was the dominant adsorption mechanism and the hydration process and the smaller particle size of MgO may play a key role in the superior phosphate removal by UMB. Removal tests in real low-concentration phosphate water samples showed that 0.05 g L<sup>-1</sup> UMB could reduce the phosphate concentration from 0.17 mg P L<sup>-1</sup> to 0.01 mg P L<sup>-1</sup>. In addition, phosphate could be desorbed from UMB in varying environments, and therefore has the potential to be used in fertilizer production or directly as a slow-release fertilizer.</p>","PeriodicalId":312,"journal":{"name":"Environmental Research","volume":" ","pages":"120518"},"PeriodicalIF":7.7,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142783587","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Carbon catabolite repression during the simultaneous utilization of lignocellulose-derived sugars in lactic acid production: Influencing factors and mitigation strategies. 在乳酸生产中同时利用木质纤维素衍生糖时碳分解代谢抑制:影响因素和缓解策略。
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-11-29 DOI: 10.1016/j.envres.2024.120484
Mingxi Li, Wenbin Zhu, Jiamei Fan, Ming Gao, Xiaona Wang, Chuanfu Wu, Ying Wang, Yuan Lu

Lignocellulose is the most abundant, sustainable, and comparatively economical renewable biomass containing ample fermentable sugars for bio-based chemical production, such as lactic acid (LA). LA is a versatile chemical with substantial global demand. However, the concurrent utilization of mixed sugars derived from lignocellulose, including glucose, xylose, and arabinose, remains a formidable challenge because of the metabolic regulation of carbon catabolite repression (CCR), in which glucose is preferentially utilized over non-glucose sugars, resulting in the loss of carbon resources and a decrease in biorefinery efficacy. Most current studies on CCR have concentrated on elucidating the principles and their impact on specific bacterial species using mixed carbon sources. However, there remains a notable dearth of comprehensive reviews summarizing the underlying principles and corresponding mitigation strategies across other bacterial strains encountering similar challenges. In light of this, this article delineates the possible factors that lead to CCR, including signal transduction and metabolic pathways. Additionally, the fermentation conditions and nutrients are described. Finally, this study proposes appropriate mitigation strategies to overcome the aforementioned obstacles and presents new insights into the rapid and simultaneous consumption of mixed sugars to bolster the production yields of biofuels and chemicals in the future.

木质纤维素是最丰富、可持续和相对经济的可再生生物质,含有充足的可发酵糖,用于生物基化学生产,如乳酸(LA)。LA是一种用途广泛的化学品,全球需求巨大。然而,同时利用来自木质纤维素的混合糖,包括葡萄糖、木糖和阿拉伯糖,仍然是一个巨大的挑战,因为碳分解代谢抑制(CCR)的代谢调节,其中葡萄糖优先于非葡萄糖被利用,导致碳资源的损失和生物炼制效率的降低。目前对混合碳源CCR的研究大多集中在阐明混合碳源CCR的原理及其对特定菌种的影响。然而,对于其他遇到类似挑战的细菌菌株的基本原理和相应的缓解策略的综合综述仍然明显缺乏。鉴于此,本文概述了导致CCR的可能因素,包括信号转导和代谢途径。此外,还描述了发酵条件和营养成分。最后,本研究提出了适当的缓解策略,以克服上述障碍,并对混合糖的快速和同时消耗提出了新的见解,以提高未来生物燃料和化学品的产量。
{"title":"Carbon catabolite repression during the simultaneous utilization of lignocellulose-derived sugars in lactic acid production: Influencing factors and mitigation strategies.","authors":"Mingxi Li, Wenbin Zhu, Jiamei Fan, Ming Gao, Xiaona Wang, Chuanfu Wu, Ying Wang, Yuan Lu","doi":"10.1016/j.envres.2024.120484","DOIUrl":"10.1016/j.envres.2024.120484","url":null,"abstract":"<p><p>Lignocellulose is the most abundant, sustainable, and comparatively economical renewable biomass containing ample fermentable sugars for bio-based chemical production, such as lactic acid (LA). LA is a versatile chemical with substantial global demand. However, the concurrent utilization of mixed sugars derived from lignocellulose, including glucose, xylose, and arabinose, remains a formidable challenge because of the metabolic regulation of carbon catabolite repression (CCR), in which glucose is preferentially utilized over non-glucose sugars, resulting in the loss of carbon resources and a decrease in biorefinery efficacy. Most current studies on CCR have concentrated on elucidating the principles and their impact on specific bacterial species using mixed carbon sources. However, there remains a notable dearth of comprehensive reviews summarizing the underlying principles and corresponding mitigation strategies across other bacterial strains encountering similar challenges. In light of this, this article delineates the possible factors that lead to CCR, including signal transduction and metabolic pathways. Additionally, the fermentation conditions and nutrients are described. Finally, this study proposes appropriate mitigation strategies to overcome the aforementioned obstacles and presents new insights into the rapid and simultaneous consumption of mixed sugars to bolster the production yields of biofuels and chemicals in the future.</p>","PeriodicalId":312,"journal":{"name":"Environmental Research","volume":" ","pages":"120484"},"PeriodicalIF":7.7,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142765145","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Associations between per- and polyfluoroalkyl substances (PFAS) and female sexual function in a preconception cohort. 在孕前队列中,全氟和多氟烷基物质(PFAS)与女性性功能的关系
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-05 DOI: 10.1016/j.envres.2024.120556
Samantha Schildroth, Julia C Bond, Amelia K Wesselink, Jasmine Abrams, Antonia M Calafat, Julianne Cook Botelho, Katharine O White, Ganesa Wegienka, Elizabeth E Hatch, Lauren A Wise

Background: Female sexual function is important for sexual well-being, general health, fertility, and relationship satisfaction. Distressing impairments in sexual function, clinically recognized as female sexual dysfunction (FSD), can manifest as issues with interest/desire, arousal, orgasm, and pain during vaginal penetration. Some evidence suggests that exposure to endocrine-disrupting chemicals may adversely affect female sexual function, but associations for per- and polyfluoroalkyl substances (PFAS) have not been previously evaluated.

Objective: We investigated associations between serum PFAS concentrations and female sexual function among U.S. pregnancy planners.

Methods: We used cross-sectional data from participants from Pregnancy Study Online (PRESTO), a prospective preconception cohort study. Participants reported sexual function and distress at baseline on two validated measures: a modified version of the Female Sexual Function Index-6 (FSFI-6) and the Female Sexual Distress Scale (FSDS). We quantified PFAS serum concentrations in samples collected in the preconception period (i.e., at baseline) using solid phase extraction-high performance liquid chromatography-isotope-dilution-mass spectrometry. Participants reported sociodemographic information on structured baseline questionnaires. We included 78 participants with complete PFAS and sexual function data and fit multivariable linear regression models to estimate mean differences in FSFI-6 scores (β) or percent differences (%) in FSDS scores per interquartile range (IQR) increase in PFAS concentrations, adjusting for age, annual household income, years of education, parity, and body mass index. We further investigated effect measure modification by parity (parous vs. nulliparous) in stratified models.

Results: An IQR increase in perfluorohexanesulfonic acid was associated with a 1.0-point decrease (95% CI = -1.8, -0.1) in reported FSFI-6 scores, reflecting poorer sexual function. PFAS were consistently associated with lower FSFI-6 scores among parous participants. PFAS were also associated, though imprecisely, with greater sexual distress.

Conclusion: Some PFAS were associated with poorer sexual function among U.S. pregnancy planners, but future studies are needed to clarify the extent to which PFAS influences female sexual health.

背景:女性性功能对性健康、一般健康、生育能力和关系满意度都很重要。令人痛苦的性功能障碍,在临床上被认为是女性性功能障碍(FSD),可以表现为兴趣/欲望、性唤起、性高潮和阴道插入时的疼痛问题。一些证据表明,接触干扰内分泌的化学物质可能对女性性功能产生不利影响,但对全氟烷基物质和多氟烷基物质(PFAS)的关联此前尚未进行评估。目的:研究美国计划怀孕者血清PFAS浓度与女性性功能之间的关系。方法:我们使用来自在线妊娠研究(PRESTO)参与者的横断面数据,这是一项前瞻性孕前队列研究。参与者在基线上报告了两种有效的性功能测量:女性性功能指数-6 (FSFI-6)和女性性困扰量表(FSDS)的修改版本。我们使用固相萃取-高效液相色谱-同位素稀释-质谱法定量了孕前(即基线)收集的样品中PFAS的血清浓度。参与者在结构化基线问卷上报告社会人口统计信息。我们纳入了78名具有完整PFAS和性功能数据的参与者,并拟合多变量线性回归模型,以估计PFAS浓度每四分位数范围(IQR)增加的FSDS分数的平均差异(β)或百分比差异(%),调整年龄、家庭年收入、受教育年限、平价和体重指数。在分层模型中,我们进一步研究了胎次(已产与未产)对效应测量的修正。结果:全氟己磺酸的IQR增加与报告的FSFI-6评分下降1.0分(95% CI=-1.8, -0.1)相关,反映出性功能较差。在已生育的参与者中,PFAS始终与较低的FSFI-6评分相关。PFAS也与更大的性困扰有关,尽管不准确。结论:一些PFAS与美国计划生育女性的性功能低下有关,但需要进一步的研究来阐明PFAS对女性性健康的影响程度。
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引用次数: 0
Distribution characteristics, source analysis and ecological risk assessment of PAHs in tea garden soil in China. 中国茶园土壤中多环芳烃分布特征、来源分析及生态风险评价
IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2025-02-01 Epub Date: 2024-12-05 DOI: 10.1016/j.envres.2024.120559
Jinzhi Li, Jiantao Xue, Yan Tan, Mingmin Jia, Junjun Feng, Xueqing Feng, Ningguo Zheng, Haoxin Fan, Huaiying Yao

In this study, we collected 177 soil samples from major tea-producing areas in China, systematically investigated the spatial distribution characteristics of the polycyclic aromatic hydrocarbons (PAHs) in the soil of these tea plantations and discussed the environmental factors influencing of the PAHs in tea garden soil. The feature ratio method and source analysis methods were used to determine the PAHs source in tea garden soil, and the potential risk of PAHs in tea garden soil was also evaluated. The results showed that the concentrations of the 16 PAHs in 177 samples ranged from 6.21 to 4068.91 ng g-1, with an average of 257.00 ng g-1. The majority of PHAs in tea garden soils predominantly contained a 5-6 ring pattern, and the highest content was indeno (1,2,3-cd) pyrene (InP, 23%) and benzo (b) fluoranthrene (BbF, 16%). In addition, 10.16% of the PAHs in tea plantation soils contained a 2-3-ring pattern, with naphthalene (NAP) having the highest content. PAH source in Chinese tea garden soil was predominantly mixed combustion, such as incomplete biomass combustion, petroleum combustion, coal combustion and wood combustion. The PAHs distribution was mainly affected by the industrial structure, geographical location of tea plantation, climatic conditions, soil properties and other factors in different regions. According to the Dutch Maliszewska-Kordybach grading standard, 79% of the soil samples from Chinese tea plantations were classified as unpolluted, 13% as mildly polluted, and 2% and 6% as moderately and severely polluted, respectively. Although the PAH pollution in tea plantations was generally low, BaP and InP pose significant ecological risk in some areas. Therefore, strategies such as effective guidelines and environmentally friendly technologies, must be developed to reduce the risk of PAH pollution in tea plantation soils.

本研究以中国主要产茶区177个土壤样品为研究对象,系统调查了茶园土壤中多环芳烃(PAHs)的空间分布特征,并探讨了影响茶园土壤多环芳烃含量的环境因素。采用特征比法和源分析方法确定茶园土壤中多环芳烃的来源,并对茶园土壤中多环芳烃的潜在风险进行评价。结果表明,177份样品中16种多环芳烃的浓度范围为6.21 ~ 4068.91 ng·g-1,平均为257.00 ng·g-1。茶园土壤中大部分多环芳烃以5 ~ 6环型为主,其中吲哚(1,2,3-cd)芘(InP, 23%)和苯并(b)芴(BbF, 16%)含量最高。此外,茶园土壤中多环芳烃(PAHs)有10.16%为2-3环型,其中萘(NAP)含量最高。中国茶园土壤中多环芳烃源以混合燃烧为主,如生物质不完全燃烧、石油燃烧、煤燃烧和木材燃烧。不同区域多环芳烃分布主要受产业结构、茶园地理位置、气候条件、土壤性质等因素影响。根据荷兰Maliszewska-Kordybach分级标准,中国茶园土壤样本中79%为未污染,13%为轻度污染,2%为中度污染,6%为重度污染。茶园的多环芳烃污染总体较低,但部分地区的酚类化合物(BaP)和酚类化合物(InP)存在较大的生态风险。因此,必须制定有效的指导方针和环境友好型技术等策略来降低茶园土壤中多环芳烃污染的风险。
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Environmental Research
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