Toxic mechanisms of the antiviral drug arbidol on microalgae in algal bloom water at transcriptomic level.

Increasing antivirals in surface water caused by their excessive consumption pose serious threats to aquatic organisms. Our recent research found that the input of antiviral drug arbidol to algal bloom water can induce acute toxicity to the growth and metabolism of Microcystis aeruginosa, resulting in growth inhibition, as well as decrease in chlorophyll and ATP contents. However, the toxic mechanisms involved remained obscure, which were further investigated through transcriptomic analysis in this study. The results indicated that 885-1248 genes in algae were differentially expressed after exposure to 0.01-10.0 mg/L of arbidol, with the majority being down-regulated. Analysis of commonly down-regulated genes found that the cellular response to oxidative stress and damaged DNA bonding were affected, implying that the stress defense system and DNA repair function of algae might be damaged. The down-regulation of genes in porphyrin metabolism, photosynthesis, carbon fixation, glycolysis, tricarboxylic acid cycle, and oxidative phosphorylation might inhibit chlorophyll synthesis, photosynthesis, and ATP supply, thereby hindering the growth and metabolism of algae. Moreover, the down-regulation of genes related to nucleotide metabolism and DNA replication might influence the reproduction of algae. These findings provided effective strategies to elucidate toxic mechanisms of contaminants on algae in algal bloom water.

Algal Extracellular Organic Matter Induced Photochemical Oxidation of Mn(II) to Solid Mn Oxide: Role of Mn(III)-EOM Complex and Its Ability to Remove 17α-Ethinylestradiol.

Photosensitizer-mediated abiotic oxidation of Mn(II) can yield soluble reactive Mn(III) and solid Mn oxides. In eutrophic water systems, the ubiquitous algal extracellular organic matter (EOM) is a potential photosensitizer and may have a substantial impact on the oxidation of Mn(II). Herein, we focused on investigating the photochemical oxidation process from Mn(II) to solid Mn oxide driven by EOM. The results of irradiation experiments demonstrated that the generation of Mn(III) intermediate was crucial for the successful photo oxidization of Mn(II) to solid Mn oxide mediated by EOM. EOM can serve as both a photosensitizer and a ligand, facilitating the formation of the Mn(III)-EOM complex. The complex exhibited excellent efficiency in removing 17α-ethinylestradiol. Furthermore, the complex underwent decomposition as a result of reactions with reactive intermediates, forming a solid Mn oxide. The presence of nitrate can enhance the photochemical oxidation process, facilitating the conversion of Mn(II) to Mn(III) and then to solid Mn oxide. This study deepens our grasp of Mn(II) geochemical processes in eutrophic water and its impact on organic micropollutant fate.

The environmental risks of antiviral drug arbidol in eutrophic lake: Interactions with Microcystis aeruginosa.

The environmental risks resulting from the increasing antivirals in water are largely unknown, especially in eutrophic lakes, where the complex interactions between algae and drugs would alter hazards. Herein, the environmental risks of the antiviral drug arbidol towards the growth and metabolism of Microcystis aeruginosa were comprehensively investigated, as well as its biotransformation mechanism by algae. The results indicated that arbidol was toxic to Microcystis aeruginosa within 48 h, which decreased the cell density, chlorophyll-a, and ATP content. The activation of oxidative stress increased the levels of reactive oxygen species, which caused lipid peroxidation and membrane damage. Additionally, the synthesis and release of microcystins were promoted by arbidol. Fortunately, arbidol can be effectively removed by Microcystis aeruginosa mainly through biodegradation (50.5% at 48 h for 1.0 mg/L arbidol), whereas the roles of bioadsorption and bioaccumulation were limited. The biodegradation of arbidol was dominated by algal intracellular P450 enzymes via loss of thiophenol and oxidation, and a higher arbidol concentration facilitated the degradation rate. Interestingly, the toxicity of arbidol was reduced after algal biodegradation, and most of the degradation products exhibited lower toxicity than arbidol. This study revealed the environmental risks and transformation behavior of arbidol in algal bloom waters.

Occurrence and cycle of dissolved iron mediated by humic acids resulting in continuous natural photodegradation of 17α-ethinylestradiol.

17α-ethinylestradiol (EE2), a synthetic endocrine-disrupting chemical, can degrade in natural waters where humic acids (HA) and dissolved iron (DFe) are present. The iron is mostly bound in Fe(III)-HA complexes, the formation process of Fe(III)-HA complexes and their effect on EE2 degradation were explored in laboratory experiments. The mechanism of ferrihydrite facilitated by HA was explored with results indicating that HA facilitated the dissolution of ferrihydrite and the generation of Fe(III)-HA complexes with the stable chemical bonds such as C-O, CO in neutral, alkaline media with a suitable Fe/C ratio. 1O2, •OH, and 3HA* were all found to be important in the photodegradation of EE2 mediated by Fe(III)-HA complexes. Fe(III)-HA complexes could produce Fe(II) and hydrogen peroxide (H2O2) to create conditions suitable for photo-Fenton reactions at neutral pH. HA helped to maintain higher dissolved iron concentrations and alter the Fe(III)/Fe(II) cycling. The natural EE2 photodegradation pathway elucidated here provides a theoretical foundation for investigating the natural transformation of other trace organic contaminants in aquatic environments.

Dissolved organic matter accelerates microbial degradation of 17 alpha-ethinylestradiol in the presence of iron mineral.

Dissolved organic matter (DOM) and iron minerals widely existing in the natural aquatic environment can mediate the migration and transformation of organic pollutants. However, the mechanism of interaction between DOM and iron minerals in the microbial degradation of pollutants deserves further investigation. In this study, the mechanism of 17 alpha-ethinylestradiol (EE2) biodegradation mediated by humic acid (HA) and three kinds of iron minerals (goethite, magnetite, and pyrite) was investigated. The results found that HA and iron minerals significantly accelerated the biodegradation process of EE2, and the highest degradation efficiency of EE2 (48%) was observed in the HA-mediated microbial system with pyrite under aerobic conditions. Furthermore, it had been demonstrated that hydroxyl radicals (HO•) was the main active substance responsible for the microbial degradation of EE2. HO• is primarily generated through the reaction between hydrogen peroxide secreted by microorganisms and Fe(II), with aerobic conditions being more conducive. The presence of iron minerals and HA could change the microbial communities in the EE2 biodegradation system. These findings provide new information for exploring the migration and transformation of pollutants by microorganisms in iron-rich environments.

Sunlight-induced degradation of COVID-19 antivirals arbidol in natural aquatic environments: Mechanisms, pathways and toxicity.

Insights into COVID-19 antivirals' environmental fate and ecological risk are urgently required due to their increasing concentrations in aquatic environments, which have rarely been studied. Herein, we first investigated the photochemical transformation and the resulting alterations in toxicity of arbidol, an antiviral drug with relatively higher toxicity. The photolysis of arbidol was rapid with a rate constant of 0.106 min-1 due to its superior ultraviolet light absorption, in which the direct photolysis was predominated with a contribution of 91.5%. Despite its substantial photolysis, only 14.45% of arbidol was mineralized after 100 min, implying that arbidol and its products might have a long-term impact on aquatic environment. It was inferred that arbidol was photolyzed mainly via the loss of thiophenol, bromine, and alkylamine, based on twelve photolytic products identified. Notably, the experimental results demonstrated that the photolysis process increased the acute toxicity of arbidol, and the toxicity prediction indicated that the ecotoxicity of two photolytic products was very high with LC50 values below 0.1 mg/L. Due to the co-effect of multiple constituents, the photolytic rate observed in wastewater treatment plant effluent and in river water was comparable to that in ultra-pure water, while it was slightly enhanced in lake water. The presence of dissolved organic matter suppressed arbidol photolysis, while NO3- exhibited a promotion effect. These results would be of great significance to assess the fate and risk of COVID-19 antivirals in natural aquatic environments.

Dynamic simulation of a motor longitudinally mounted on a centralized electric drive systems for pure electric vehicles under torque ripple and transmission error excitations.

The dynamic characteristics of electric drive systems are crucial in electric vehicles. Based on the dynamic finite element method and previous studies, this study proposes and analyzes a new mathematical model for a motor longitudinally mounted on a centralized electric drive system of a pure electric vehicle. First, we analyze the largest torque ripple of a fractional slot concentrated winding inner-mounted permanent magnet synchronous motor designed for commercial electric vehicles. This torque ripple is identified as one of the excitations influencing the dynamic performance of the electric drive system. Second, a new dynamic mathematical model for the electric drive system is established. Third, we investigate the linear vibration responses of the system subject to torque ripple and transmission error. Finally, the relationships between critical motor parameters and dynamic mesh force are revealed. The results demonstrate that the proposed theoretical method can effectively determine the dynamic characteristics of the electric drive system, thereby providing valuable theoretical guidance for the design and optimization of the motor and electric drive system.

Investigation of the luminescence properties and energy transfer mechanisms in Gd3TaO7:Bi3+,Eu3+ phosphors for their potential application in full-spectrum WLEDs.

In recent years, there has been increasing effort devoted to the development of single-phase white phosphors due to drawbacks such as severe reabsorption and color deviation in traditional white light-emitting diodes (WLEDs). A new feasible strategy has emerged for achieving white light emission through the Bi3+-Eu3+ energy transfer in suitable single-phase phosphors. Therefore, a series of Gd3TaO7:xBi3+ and Gd3TaO7:0.01Bi3+,yEu3+ phosphors were synthesized via a high-temperature solid-state method, and their properties were systematically characterized. In Gd3TaO7, Bi3+ occupies two kinds of Gd3+ site, resulting in two broad emission bands peaking at 427 nm and 500 nm respectively under ultraviolet (UV) excitation, which arise from 3P1 → 1S0 transitions. By adjusting the concentration of Eu3+ in Gd3TaO7:0.01Bi3+,yEu3+, effective energy transfer can occur between Bi3+ and Eu3+, thus enabling the regulation of green-white-red luminescence under 332 nm excitation and blue-white-red luminescence under 365 nm UV light irradiation. Upon stimulation with a 365 nm UV chip, Gd3TaO7:0.01Bi3+,0.02Eu3+ emits white light with CIE coordinates of (0.3509, 0.3202), a color temperature of 4629 K, and an impressive color rendering index of 87.96. The above results indicate the potential of Gd3TaO7:0.01Bi3+,yEu3+ phosphor as a viable candidate for WLED applications.

Variation in photochemical properties of dissolved black carbon during bio-transformation and iron mineral fractionation process.

The excellent photochemical properties of dissolved black carbon (DBC) have been proven to be a significant contributor to the removal of organic pollutants in environment. However, the photochemical properties of DBC will inevitably be changed during biotic and abiotic processes. Herein, the structures and compositions of DBC during bio-transformation and goethite adsorption processes were comprehensively studied, and their corresponding photochemical properties were also evaluated. Bio-transformed DBC (B-DBC) contained more aromatic, high molecular weight, and phenolic substances compared with pristine DBC (P-DBC). The photodegradation of 17α-ethynylestradiol (EE2) was significantly promoted by B-DBC because of its superior capacity for producing 3DBC*. Moreover, the subsequent goethite fractionation selectively reduced the parts of components with high aromaticity and carboxylic functional groups in B-DBC. The interaction between B-DBC and goethite resulted in the release of Fe2+ into goethite-fractionated DBC (G-DBC), which induced the photodegradation mechanism of EE2 shifting from a single-electron transfer driven by 3DBC⁎ to the oxidation of •OH. This study provides valuable insights into the changes in photochemical behavior of DBC resulting from biotic or abiotic processes, and enhances our understanding of the role of DBC in the fate of organic pollutants.

The photolytic behavior of COVID-19 antivirals ribavirin in natural waters and the increased environmental risk.

Increasing drug residues in aquatic environments have been caused by the abuse of antivirals since the global spread of the COVID-19 epidemic, whereas research on the photolytic mechanism, pathways and toxicity of these drugs is limited. The concentration of COVID-19 antivirals ribavirin in rivers has been reported to increase after the epidemic. Its photolytic behavior and environmental risk in actual waters such as wastewater treatment plant (WWTP) effluent, river water and lake water were first investigated in this study. Direct photolysis of ribavirin in these media was limited, but indirect photolysis was promoted in WWTP effluent and lake water by dissolved organic matter and NO3-. Identification of photolytic intermediates suggested that ribavirin was photolyzed mainly via C-N bond cleavage, splitting of the furan ring and oxidation of the hydroxyl group. Notably, the acute toxicity was increased after ribavirin photolysis owing to the higher toxicity of most of the products. Additionally, the overall toxicity was greater when ARB photolysis in WWTP effluent and lake water. These findings emphasize the necessity to concern about the toxicity of ribavirin transformation in natural waters, as well as to limit its usage and discharge.

Algal organic matter and dissolved Mn cooperatively accelerate 17α-ethinylestradiol photodegradation: Role of photogenerated reactive Mn(III).

Algal extracellular organic matter (EOM), a major fraction of the dissolved organic matter found in eutrophic plateau lakes, can act as a photosensitizer to drive the abiotic oxidation of Mn(II). This process has the potential to generate reactive Mn(III) and influence the fate of organic pollutants. In this study, the photodegradation of 17α-ethinylestradiol (EE2) in the presence of Mn(II) and EOM was investigated with emphasis on the photogeneration mechanism of Mn(III). The results indicated that Mn(II) can accelerate EE2 photodegradation in EOM solution owing to the photogeneration of reactive Mn(III), and the enhancement was greater at higher Mn(II) concentrations. The generation of reactive Mn(III) was mainly attributable to the action of superoxide radical generated by photosensitization of EOM. In addition, the photodegradation of EE2 was slower at higher pH, possibly because of the deactivation of Mn(III) under alkaline conditions. Single-electron transfer was an indispensable process in the photodegradation. The differences in fluorophore content, pH, and NO3- concentrations are all important determinants for EE2 photodegradation in natural waters. The information obtained in this research would contribute to the understanding of reactions between Mn(II) and EOM, and provide new insights into the behaviors of reactive Mn(III) in eutrophic water irradiated by sunlight.

The efficient treatment of mature landfill leachate using tower bipolar electrode flocculation-oxidation combined with electrochemical biofilm reactors.

Mature landfill leachate contains high concentrations of organic and inorganic compounds that inhibit the performance of conventional biological treatment. Nowadays, few single treatment techniques could fulfill the requirements of cleaning mature landfill leachate. In this study, a tower bipolar electrode flocculation-oxidation (BEF-O) reactor and an electrochemical biofilm reactor (EBR) combine device was constructed to effectively treat mature landfill leachate. And the removal efficiency and mechanism of various pollutants using the BEF-O reactor were investigated. The BEF-O system with the current density of 100 mA/cm2 shows excellent treatment efficiency, which can roundly remove most pollutants (NH4+-N, COD and heavy metals, etc.), and increase the bioavailability of the effluent to facilitate subsequent EBR treatment. Benefiting from the metabolic stimulation and population selection effect of electric current on microorganisms, EBR has a denser biofilm, stronger anti-pollution load capacity, superior, and stable pollution treatment efficiency. More importantly, the combined device can reduce the concentrations of COD and NH4+-N from 6410 to 338 mg/L and 4065 to 4 mg/L, respectively, and has an economical energy consumption of 32.02 kWh/(kg COD) and 54.04 kWh/ (kg NH4+-N). To summarize, this research could provide an innovative and industrial application prospect technology for the mature landfill leachate treatment.

Photoaging mechanisms of microplastics mediated by dissolved organic matter in an iron-rich aquatic environment.

As emerging pollutants, microplastics (MPs) have aroused worldwide concern due to their ubiquitous distribution, environmental persistence, and potential ecological risks. However, the ageing mechanisms, environmental behaviours and risks of photoaged MPs mediated by environmental factors remain obscure. Herein, systems containing a light source, humic acid (HA) and Fe were established to investigate the natural photoaging process of MPs including polyvinyl chloride (PVC) and polyethylene terephthalate (PET). The dehydrochlorination reaction of PVC-MP was inhibited by HA and Fe, which resulted from the coeffect of photon competition, excited state quenching, radical deactivation or transformation, and defect structure destruction. In contrast, the enhanced fluorescence effect suggested that the photooxidation reactions of PET-MP were promoted by HA and Fe. Therefore, the presence of HA and Fe in the environment inhibited the photoreduction of MPs while favoring the photooxidative process. Additionally, the adsorption capacity for 17α-ethinylestradiol and the cytotoxicity of MPs were increased after ageing in the hv + HA and hv + HA + Fe systems, which was attributed to the changes in morphology, elements and functional groups. This study provided new insight into the ageing behaviours of MPs in the natural environment with widespread dissolved organic matter and Fe.

The desorption mechanism of dissolved organic matter on pollutants and the change of biodiversity during sediment dredging.

Sediment dredging is an effective means to control the endogenous pollution of lakes, which could significantly change the concentration and composition of organic matter, especially dissolved organic matter (DOM) in the lake. DOM is particularly important for the release of endogenous pollutants, which will inevitably bring an impact on aquatic biodiversity. Nevertheless, in recent research little attention has been paid to the desorption mechanism of DOM on pollutants and the change of biodiversity during dredging. This study investigated the physicochemical properties of DOM in the sediment by taking a sediment dredging project in Dianchi Lake in China for example. The correlations of DOM properties with the desorption behavior of nitrogen (N), phosphorus (P), cadmium (Cd), lead (Pb) and the biodiversity of aquatic organisms were analyzed. The results show that the aromaticity and humification of DOM were improved after dredging, and the high molecular weight DOM was degraded into low molecular weight substance. The desorption amount of N, P and heavy metals (Cd, Pb) were decreased as the pH values increased. Moreover, NH4+-N promoted the release of Pb2+ from DOM, while the release of PO43--P was inhibited. Correlation analysis shows that the physicochemical properties of DOM exactly affected the release of N, P, Cd and Pb. It was easier to desorb pollutants with low aromaticity and humification of DOM, leading to a decrease in the diversity of aquatic organisms. This study identified the desorption mechanism of endogenous pollutants in DOM and the ecological risk to aquatic organisms, providing a theoretical basis for the prevention and control of water pollution.

Assessment technologies of rail systems' structural adequacy - A review from mechanical engineering perspectives.

The structural adequacy challenges of railroad track structures have received considerable attention globally. Track defects and failures due to weak strength and buckling effect account for one-third of all railroad accidents. The current paper provides a comprehensive study of the recent work on the structural adequacy/bearing capacity of rail systems from mechanical engineering perspectives; existing techniques for track stiffness/modulus evaluations, including standstill and continuous methods. Further, this paper demonstrates the current techniques for track stiffness/modulus evaluation. Prevailing track modulus techniques, while accurate but time-taking, effortful, requires a track closure and provides only single-point information. Also, this review provides a suggestion on the non-destructive and non-invasive technologies for example Ground-penetrating radar (GPR) and evaluation of the substructures of tracks as they have great potential for image subsurface features.

The distribution and risk of microplastics discharged from sewage treatment plants in terrestrial and aquatic compartment.

Many microplastics (MPs) were produced in daily life, which would enter sewage treatment plants (STPs) with the wastewater. Although the STPs has a good interception effect on these MPs, there will still be a part of MPs entering the environment with the effluent and sludge treatment, causing a certain ecological risk. This study investigated the abundance, characteristics and retention of MPs in different STPs, as well as the ecological risks caused by MPs entering the environment. The abundance of MPs in influent and effluent was ranged from 2.02 to 2.50 items L-1 and 0.27-0.48 items L-1, respectively. The abundance of MPs in dewatered sludge and sediment of Lake Dianchi was ranged from 3.719-6.949 × 103 items (kg Ds)-1 and 1.84-5.23 × 103 items (kg Ds)-1, respectively. So roughly 80% of the MPs were trapped and transferred into the dewatered sludge. The observed colors of MPs were transparent, black, blue, red, pale brown, green and gray, and their main species were polypropylene (PP) and polyethylene (PE). To further evaluate the ecological risks of MPs, the oyster mushroom was cultivated in a medium supplemented with MPs. It was found that MPs could be absorbed by oyster mushrooms with a 7-11% of absorption rate, the fibers were widely distributed in the stipes and the pileus. This study had theoretical significance for exploring the distribution of MPs in STPs and clarifying the ecological risk posed by MPs in the environment.