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Strikingly, the wastewater from a pharmaceutical factory producing Chinese medicine was also rich in bacA, sul1, mexW, mexB, mexF and oprn. It can be seen from the co-occurrence patterns that pathogens and the main ARGs have strong co-occurrence. Higher abundance of offensive virulence factors in industrial wastewater and their strong correlation with pathogens containing ARGs suggest higher microbiological risk. These findings highlight the need to assess ARG acquisition by pathogens in the surface water of human-impacted environments where pathogens and ARGs may co-thrive.Biochar was proved as an electron shuttle to facilitate extracellular electron transfer (EET) of electrochemically active bacteria (EAB); however, its underlying mechanism was not fully understood. In this study, we aimed to further explore how the regulation of surface functional groups of biochar would affect the microbial iron reduction process of Geobacter sulfurreducens as a typical EAB. Two modified biochars were achieved after HNO3 (NBC) and NaBH4 (RBC) pretreatments, and a control biochar was produced after deionized water (WBC) washing. Results showed that WBC and RBC significantly accelerated microbial iron reduction of G. sulfurreducens PCA, while had no effect in the final Fe (II) minerals (e.g., vivianite and green rust (CO32-)). Besides, Brunauer-Emmett-Teller (BET) surface area, electron spin resonance (ESR) and electrochemical measurements showed that larger surface area, lower redox potential, and more redox-active groups (e.g., aromatic structures and quinone/hydroquinone moieties) in RBC explained its better electron transfer performance comparing to WBC. Interestingly, NBC completely suppressed the Fe (III) reduction process, mainly due to the production of reactive oxygen species which inhibited the growth of G. sulfurreducens PCA. Overall, this work paves a feasible way to regulate the surface functional groups for biochar, and comprehensively revealed its effect on EET process of microorganisms.Although the toxicity of microplastics (MPs) and nanoplastics (NPs) is recognized at different trophic levels, our know-how about their effects on amphibians is limited. Thus, we present and discuss the current state on studies involving amphibians and plastic particles, based on a broad approach to studies published in the last 5 years. To search for the articles, the ISI Web of Science, ScienceDirect, and Scopus databases were consulted, using different descriptors related to the topic of study. After the systematic search, we identified 848 publications. Of these, 12 studies addressed the relationship "plastic particles and amphibians" (7 studies developed in the laboratory and 5 field studies). The scientometric analysis points to geographic concentration of studies in Brazil and China; low investment in research in the area, and limited participation of international authors in the studies carried out. In the systematic approach, we confirm the scarcity of available data on the toxicity of plastic particles in amphibians; we observed a concentration of studies in the Anura order, only one study explored the toxicological effects of NPs and polystyrene and polyethylene are the most studied plastic types. https://www.selleckchem.com/products/cpi-1205.html Moreover, the laboratory tested concentrations are distant from those of the environmentally relevant; and little is known about the mechanisms of action of NPs/MPs involved in the identified (eco)toxicological effects. Thus, we strongly recommend more investments in this area, given the ubiquitous nature of NPs/MPs in aquatic environments and their possible consequences on the dynamics, reproduction, and survival of species in the natural environment.Sulfamethoxazole (SMX) is a widely distributed emerging contaminant, which will bring serious harm to ecology and human health. Herein, evaluation of ozone (O3) coupled with calcium peroxide (CaO2) for SMX elimination was carried out. The results showed that CaO2 could promote SMX elimination in O3 system. The removal efficiency was improved from 65.6% to 73.9% when the CaO2 dosage was 0.06 g L-1. O3 dosage of 0.55 g h-1 was beneficial to SMX degradation. With decrease of initial SMX concentration, the removal of SMX firstly enhanced and then declined. Compared with alkaline, acidic and neutral conditions were favorable for SMX degradation. ROS including ?OH, ?O2- and 1O2 play critical role for SMX degradation. Synergetic effect could be established between O3 and CaO2, which encouraged formation of ?OH and accelerated SXM decomposition. The total organic carbon (TOC) and chemical oxygen demand (COD) were all declined after O3/CaO2 treatment. According to results of liquid chromatography-mass spectrometry (LC-MS) and references, four major pathways were proposed. The O3/CaO2 technology was also suitable for practical wastewater treatment. QSAR calculation and seed germination experiment showed that toxicity of the treatment solution was alleviated after O3/CaO2 treatment.Sulfonamide antibiotics (SAs) are used on a large scale in human and veterinary medicine. The main goal of this study was to develop a method for the detection of selected SAs (sulfamethoxazole, sulfadiazine, sulfamethazine, sulfathiazole, sulfapyridine, sulfamerazine, sulfamethiazole, and sulfisoxazole) in aqueous samples (targeted analysis), and then conduct a non-targeted analysis to determine the transformation products to elucidate their degradation pathways. These analyses were performed using ultra-high-performance liquid chromatography coupled to tandem mass spectrometry. The procedure was used to detect selected antibiotics in water samples collected throughout a highly urbanized area. Among the studied compounds, sulfamethoxazole (max. 78.88 ng L-1) and sulfapyridine (max. 38.88 ng L -1) were the most common pollutants identified in surface waters. Trace amounts of sulfadiazine (below LOQ = 0.40 ng L-1) were also detected. Next, the samples were screened to detect the transformation products. Several sulfadiazine and sulfamethoxazole transformation products were detected and confirmed in the environmental samples.Functional nMnOx@RBC composites were synthesized via a simple co-precipitation method. The nanomaterials have efficient activity in activating peroxymonosulfate (PMS) for removal of chlorophenols (CPs). Rice husk biochar (RBC) could support nMnOx, and acted as an electron shuttle to mediate electron transfer reaction. nMnOx@RBC had superior catalytic and adsorption properties and exhibited remarkable synergistic effects. This led to complete degradation of 4-chloro-3-methyl phenol (CMP) in 60 min at the natural pH (7.0). Reactive oxygen species (ROS) were also identified via the corresponding scavengers. The results indicated that singlet oxygen (1O2) played a dominant role in the degradation of CMP within nMnOx@RBC system. Moreover, the mechanism of CMP decomposition was rationally proposed, and possible intermediate products were deduced. The high degradation performances of diverse CPs were also observed in nMnOx@RBC/PMS system. This research aims to offer novel insights into carbon-metal nanomaterials for the elimination of emerging pollutants.
