Genome-wide association study and genomic selection of spike-related traits in bread wheat.

KEY MESSAGE: Identification of 337 stable MTAs for wheat spike-related traits improved model accuracy, and favorable alleles of MTA259 and MTA64 increased grain weight and yield per plant. Wheat (Triticum aestivum L.) is one of the three primary global, staple crops. Improving spike-related traits in wheat is crucial for optimizing spike and plant morphology, ultimately leading to increased grain yield. Here, we performed a genome-wide association study using a dataset of 24,889 high-quality unique single-nucleotide polymorphisms (SNPs) and phenotypic data from 314 wheat accessions across eight diverse environments. In total, 337 stable and significant marker-trait associations (MTAs) related to spike-related traits were identified. MTA259 and MTA64 were consistently detected in seven and six environments, respectively. The presence of favorable alleles associated with MTA259 and MTA64 significantly reduced wheat spike exsertion length and spike length, while enhancing thousand kernel weight and yield per plant. Combined gene expression and network analyses identified TraesCS6D03G0692300 and TraesCS6D03G0692700 as candidate genes for MTA259 and TraesCS2D03G0111700 and TraesCS2D03G0112500 for MTA64. The identified MTAs significantly improved the prediction accuracy of each model compared with using all the SNPs, and the random forest model was optimal for genome selection. Additionally, the eight stable and major MTAs, including MTA259, MTA64, MTA66, MTA94, MTA110, MTA165, MTA180, and MTA164, were converted into cost-effective and efficient detection markers. This study provided valuable genetic resources and reliable molecular markers for wheat breeding programs.

Preparing for the Next Pandemic: Predicting UV Inactivation of Coronaviruses with Machine Learning.

The epidemic of coronaviruses has posed significant public health concerns in the last two decades. An effective disinfection scheme is critical to preventing ambient virus infections and controlling the spread of further outbreaks. Ultraviolet (UV) irradiation has been a widely used approach to inactivating pathogenic viruses. However, no viable framework or model can accurately predict the UV inactivation of coronaviruses in aqueous solutions or on environmental surfaces, where viruses are commonly found and spread in public places. By conducting a systematic literature review to collect data covering a wide range of UV wavelengths and various subtypes of coronaviruses, including severe acute respiratory syndrome 2 (SARS-CoV-2), we developed machine learning models for predicting the UV inactivation effects of coronaviruses in aqueous solutions and on environmental surfaces, for which the optimal test performance was obtained with R2 = 0.927, RMSE = 0.565 and R2 = 0.888, RMSE = 0.439, respectively. Besides, the required UV doses at different wavelengths to inactivate the SARS-CoV-2 to 1 Log TCID50/mL titer from different initial titers were predicted for inactivation in protein-free water, saliva on the environmental surface, or the N95 respirator. Our models are instructive for eliminating the ongoing pandemic and controlling the spread of an emerging and unknown coronavirus outbreak.

Sunlight-Mediated Reductive Transformation of Thallium(III) in Acidic Natural Organic Matter Solutions: Mechanisms and Kinetic Modeling.

Thallium (Tl) redox state determines its speciation and fate in aqueous environments. Despite the high potential of natural organic matter (NOM) providing the reactive groups to complex and reduce Tl(III), the kinetics and mechanisms by which NOM influences the Tl redox transformation have remained insufficiently understood. Here, we studied the reduction kinetics of Tl(III) in acidic Suwannee River fulvic acid (SRFA) solutions under dark and solar-irradiated conditions. Our results show that the thermal Tl(III) reduction occurs by the reactive organic moieties in SRFA, with the electron-donating capacities of SRFA increased with pH and decreased with [SRFA]/[Tl(III)] ratios. Solar irradiation promoted Tl(III) reduction in SRFA solutions as a result of ligand-to-metal charge transfer (LMCT) within the photoactive Tl(III) species as well as an additional reduction process mediated by a photogenerated superoxide. We demonstrated that the formation of Tl(III)-SRFA complexes decreased the reducibility of Tl(III), with the kinetics dependent on the nature of the binding component and SRFA concentrations. A "three ligand class" kinetics model has been developed and satisfactorily describes Tl(III) reduction kinetics over a range of experimental conditions. The insights presented here should assist in understanding and predicting the NOM-mediated speciation and redox cycle of Tl in a sunlit environment.

The brassinosteroid biosynthesis gene TaD11-2A controls grain size and its elite haplotype improves wheat grain yields.

KEY MESSAGE: TaD11-2A affects grain size and root length and its natural variations are associated with significant differences in yield-related traits in wheat. Brassinosteroids (BRs) control many important agronomic traits and therefore the manipulation of BR components could improve crop productivity and performance. However, the potential effects of BR-related genes on yield-related traits and stress tolerance in wheat (Triticum aestivum L.) remain poorly understood. Here, we identified TaD11 genes in wheat (rice D11 orthologs) that encoded enzymes involved in BR biosynthesis. TaD11 genes were highly expressed in roots (Zadoks scale: Z11) and grains (Z75), while expression was significantly suppressed by exogenous BR (24-epiBL). Ectopic expression of TaD11-2A rescued the abnormal panicle structure and plant height (PH) of the clustered primary branch 1 (cpb1) mutant, and also increased endogenous BR levels, resulting in improved grain yields and grain quality in rice. The tad11-2a-1 mutant displayed dwarfism, smaller grains, sensitivity to 24-epiBL, and reduced endogenous BR contents. Natural variations in TaD11-2A were associated with significant differences in yield-related traits, including PH, grain width, 1000-grain weight, and grain yield per plant, and its favorable haplotype, TaD11-2A-HapI was subjected to positive selection during wheat breeding. Additionally, TaD11-2A influenced root length and salt tolerance in rice and wheat at seedling stages. These results indicated the important role of BR TaD11 biosynthetic genes in controlling grain size and root length, and also highlighted their potential in the molecular biological analysis of wheat.

Light- and H2O2-Mediated Redox Transformation of Thallium in Acidic Solutions Containing Iron: Kinetics and Mechanistic Insights.

The redox transformation between the oxidation states of thallium (Tl(I) and Tl(III)) is the key to influencing its toxicity, reactivity, and mobility. Dissolved iron (Fe) is widely distributed in the environment and coexists at a high level with Tl in acidic mine drainages (AMDs). While ultraviolet (UV) light and H2O2 can directly (by inducing Tl(III) reduction) and indirectly (by inducing Fe(III) to form reactive intermediates) impact the redox cycles of Tl in Fe(III)-containing solutions, the kinetics and mechanism remain largely unclear. This study is the first to investigate the UV light- and H2O2-mediated Tl redox kinetics in acidic Fe(III) solutions. The results demonstrate that UV light and H2O2 could directly reduce Tl(III) to Tl(I), with the extent of reduction dependent on the presence of Fe(III) and the solution pH. At pH 3.0, Tl(I) was completely oxidized to Tl(III), which can be ascribed to the generation of hydroxyl radicals (•OH) from the Fe(III) photoreduction or Fe(III) reaction with H2O2. The kinetics of Tl(I) oxidation were strongly affected by the Fe(III) concentration, pH, light source, and water matrix. Kinetic models incorporating Tl redox kinetics with Fe redox kinetics were developed and satisfactorily interpreted Tl(III) reduction and Tl(I) oxidation under the examined conditions. These findings emphasize the roles of the UV light- and H2O2-driven Fe cycles in influencing the redox state of Tl, with implications for determining its mobility and fate in the environment.

Kinetics of Thallium(I) Oxidation by Free Chlorine in Bromide-Containing Waters: Insights into the Reactivity with Bromine Species.

The oxidation of thallium [Tl(I)] to Tl(III) by chlorine (HOCl) is an important process changing its removal performance in water treatment. However, the role of bromide (Br-), a common constituent in natural water, in the oxidation behavior of Tl(I) during chlorination remains unknown. Our results demonstrated that Br- was cycled and acted as a catalyst to enhance the kinetics of Tl(I) oxidation by HOCl over the pH range of 5.0-9.5. Different Tl(I) species (i.e., Tl+ and TlOH(aq)) and reactive bromine species (i.e., HOBr/BrO-, BrCl, Br2O, and BrOCl) were kinetically relevant to the enhanced oxidation of Tl(I). The oxidation by free bromine species became the dominant pathway even at a low Br- level of 50 µg/L for a chlorine dose of 2 mg of Cl2/L. It was found that the reactions of Tl+/BrCl, Tl+/BrOCl, and TlOH(aq)/HOBr dominated the kinetics of Tl(I) oxidation at pH < 6.0, pH 6.0-8.0, and pH > 8.0, respectively. The species-specific rate constants for Tl+ reacting with individual bromine species were determined and decreased in the order: BrCl > Br2 > BrOCl > Br2O > HOBr. Overall, the presented results refine our knowledge regarding the species-specific reactivity of TI(I) with bromine species and will be useful for further prediction of thallium mobility in chlorinated waters containing bromide.

Release of deposited MnO2 nanoparticles from aqueous surfaces.

Changes in solution chemistry and transport conditions can lead to the release of deposited MnO2 nanoparticles from a solid interface, allowing them to re-enter the aqueous environment. Understanding the release behavior of MnO2 nanoparticles from naturally occurring surfaces is critical for better prediction of the transport potential and environmental fate of MnO2 nanoparticles. In this study, the release of MnO2 nanoparticles was investigated using a quartz crystal microbalance with dissipation monitoring (QCM-D), and different environmental surface types, solution pH values and representative macromolecular organics were considered. MnO2 nanoparticles were first deposited on crystal sensors at elevated NaNO3 concentrations before being rinsed with double-deionized water to induce their remobilization. The results reveal that the release rate of MnO2 depends on the surface type, in the decreasing order: SiO2 > Fe3O4 > Al2O3, resulting from electrostatic interactions between the surface and particles. Moreover, differences in solution pH can lead to variance in the release behavior of MnO2 nanoparticles. The release rate from surfaces was significantly higher at pH 9.8 that at 4.5, indicating that alkaline conditions were more favorable for the mobilization of MnO2 in the aquatic environment. In the presence of macromolecular organics, bovine serum albumin (BSA) can inhibit the release of MnO2 from the surfaces due to attractive forces. In presence of humic acid (HA) and sodium alginate (SA), the MnO2 nanoparticles were more likely to be mobile, which may be associated with a large repulsive barrier imparted by steric effects.

Deposition Kinetics of Colloidal Manganese Dioxide onto Representative Surfaces in Aquatic Environments: The Role of Humic Acid and Biomacromolecules.

The initial deposition kinetics of colloidal MnO2 on three representative surfaces in aquatic systems (i.e., silica, magnetite, and alumina) in NaNO3 solution were investigated in the presence of model constituents, including humic acid (HA), a polysaccharide (alginate), and a protein (bovine serum albumin (BSA), using laboratory quartz crystal microbalance with dissipation monitoring equipment (QCM-D). The results indicated that the deposition behaviors of MnO2 colloids on three surfaces were in good agreement with classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. Critical deposition concentrations (CDC) were determined to be 15.5 mM NaNO3 and 9.0 mM NaNO3 when colloidal MnO2 was deposited onto silica and magnetite, respectively. Both HA and alginate could largely retard the deposition of MnO2 colloids onto three selected surfaces due to steric repulsion, and HA was more effective in decreasing the deposition rate relative to alginate. However, the presence of BSA can provide more attractive deposition site and thus lead to greater deposition behavior of MnO2 colloids onto surfaces. The dissipative properties of the deposited layer were also influenced by surface type, electrolyte concentration, and organic matter characteristics. Overall, these results provide insights into the deposition behavior of MnO2 colloids on environmental surfaces and have significant implications for predicting the transport potential of common MnO2 colloids in natural environments and engineered systems.

The determination of thallium in the environment: A review of conventional and advanced techniques and applications.

Thallium (Tl) is a potential toxicity element that poses significant ecological and environmental risks. Recently, a substantial amount of Tl has been released into the environment through natural and human activities, which attracts increasing attention. The determination of this hazardous and trace element is crucial for controlling its pollution. This article summarizes the advancement and progress in optimizing Tl detection techniques, including atomic absorption spectroscopy (AAS), voltammetry, inductively coupled plasma (ICP)-based methods, spectrophotometry, and X-ray-based methods. Additionally, it introduces sampling and pretreatment methods such as diffusive gradients in thin films (DGT), liquid-liquid extraction, solid phase extraction, and cloud point extraction. Among these techniques, ICP-mass spectrometry (MS) is the preferred choice for Tl detection due to its high precision in determining Tl as well as its species and isotopic composition. Meanwhile, some new materials and agents are employed in detection. The application of novel work electrode materials and chromogenic agents is discussed. Emphasis is placed on reducing solvent consumption and utilizing pretreatment techniques such as ultrasound-assisted processes and functionalized magnetic particles. Most detection is performed in aqueous matrices, while X-ray-based methods applied to solid phases are summarized which provide non-destructive analysis. This work improves the understanding of Tl determination technology while serving as a valuable resource for researchers seeking appropriate analytical techniques.

Removal of thallium by MnOx coated limestone sand filter through regeneration of KMnO4: Combination of physiochemical and biochemical actions.

Treatment of industrial thallium(Tl)-containing wastewater is crucial for mitigating environmental risks and health threats associated with this toxic metal. The incorporation of Mn oxides (MnOx) into the filtration system is a promising solution for efficient Tl(I) removal. However, further research is needed to elucidate the underlying mechanism behind MnOx-enhanced filtration and the rules of its stable operation. In this study, limestone, a cost-effective material, was selected as the filter media. Raw water with Mn(II), Tl(I), and other pollutants was prepared after a thorough investigation of actual industrial wastewater conditions. KMnO4 was added to induce the formation of MnO2 on limestone surfaces, while long-term operation led to enrichment of manganese oxidizing microorganisms (MnOM). Results revealed a dual mechanism. Firstly, most Mn(II) were oxidized by KMnO4 to form MnO2 attaching to limestone sands, and both Tl(I) and residual Mn(II) were adsorbed onto the newly formed MnO2. Subsequently, enzymes secreted by MnOM facilitated oxidation of remaining Mn(II), resulting in the generation of biogenic manganese oxides (BioMnOx) with numerous vacancies during long-term operation. The generated BioMnOx not only adsorbed Mn(II) and Tl(I) but also promoted their oxidation process. This approach offers an effective and sustainable method for removing both Mn(II) and Tl(I) from industrial wastewater, thereby addressing the challenges posed by thallium-contaminated effluents.

Photochemical transformation and immobilization of thallium in the presence of iron and arsenic: Mechanistic insights from the coupled formation of arsenate complexes.

Despite the occurrence of thallium (Tl) in the acidic mining-affected areas being highly positively correlated with iron (Fe) and arsenic (As), the effects of the two accompanying elements on Tl redox transformation and immobilization remain largely unknown. Here, we investigated the photochemical redox kinetics and immobilization efficiency of Tl for a wide range of As/Fe and As/Tl ratios under acidic conditions. We provided the first experimental confirmation of the complexation of Tl(III) with As(V) by the spectrophotometric method and revealed the role of Tl(III)-As(V) complexes in decreasing the photoreduction rate of Tl(III) under sunlight. Additionally, the negative impact of colloidal Fe(III)-As(V) and Fe(III)-As(III) complexes formation on decreasing photoactive Fe(III) speciation and thus the apparent quantum yield of •OH was highlighted, which consequently hindered the oxidative conversion of Tl(I) to Tl(III). We rationalize the kinetics results by developing the model which quantitatively describes the photochemistry of Tl. Furthermore, we demonstrated the colloid-facilitated immobilization of Tl(III) through the formation of Tl(III)-As(V) clusters and surface adsorption onto the complexes. This study broadens the mechanistic understanding of redox transformation and immobilization potential of Tl and aids in assessing Tl speciation as well as its coupled transformation with Fe and As species in the sunlit water environment.

Endoplasmic reticulum stress-induced NLRP3 inflammasome activation as a novel mechanism of polystyrene microplastics (PS-MPs)-induced pulmonary inflammation in chickens. / å† è´¨ç½‘åº”æ¿€è¯±å¯¼çš„NLRP3炎性体激活是聚苯乙烯微塑料（PS-MPs）诱导的鸡肺部炎症的新机制.

Microplastics (MPs) have attracted growing attention worldwide as an increasingly prevalent environmental pollutant. In addition, chicken meat is currently the most widely consumed kind of poultry in the global market. Consumer demand for chicken is on the rise both at home and abroad. As a result, the safety of chicken raising has also received significant attention. The lungs play an essential role in the physiological activities of chickens, and they are also the most vulnerable organs. Lung injury is difficult to repair after the accumulation of contaminants, and the mortality rate is high, which brings huge economic losses to farmers. The research on the toxicity of MPs has mainly focused on the marine ecosystem, while the mechanisms of toxicity and lung damage in chickens have been poorly studied. Thus, this study explored the effects of exposure to polystyrene microplastics (PS-MPs) at various concentrations for 42 d on chicken lungs. PS-MPs could cause lung pathologies and ultrastructural abnormalities, such as endoplasmic reticulum (ER) swelling, inflammatory cell infiltration, chromatin agglutination, and plasma membrane rupture. Simultaneously, PS-MPs increased the expression of genes related to the heat shock protein family (Hsp60, Hsp70, and Hsp90), ER stress signaling (activating transcription factor 6 (ATF6), ATF4, protein kinase RNA-like ER kinase (PERK), and eukaryotic translation initiation factor 2 subunit α (eIF2α)), pyroptosis-related genes (NOD-|, LRR- and pyrin domain-containing protein 3 (NLRP3), apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), interleukin-1ß (IL-1ß), cysteinyl aspartate-specific proteinase 1 (Caspase1), and gasdermin-D (GSDMD)), and the inflammatory signaling pathway (nuclear factor-|κB (NF-|κB), inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2)). The above results showed that PS-MP exposure could result in lung stress, ER stress, pyroptosis, and inflammation in broilers. Our findings provide new scientific clues for further research on the mechanisms of physical health and toxicology regarding MPs.

Cotransport of aged biochar colloids and thallium(I) in water-saturated porous media: Impact of the ionic strength, pH and aging degree.

Biochar colloids entering the soil undergo aging over time and exhibit strong capabilities in adsorbing and transporting pollutants. Therefore, investigating the cotransport of aged biochar colloids and thallium (Tl(I)) in quartz sand media is crucial for understanding Tl(I) migration in underground environments. This study investigated the migration of biochar colloids with two different aging degrees and Tl(I) in quartz sand media at various pH and ionic strengths (ISs). The results revealed that under all ISs and pH, 30%AWB (biochar aged with 30 % (w/w) HNO3) inhibited Tl(I) migration in media. This inhibition primarily arose from the introduction of hydroxyl and carboxyl groups during aging, which significantly enhanced colloid adsorption onto Tl(I). At lower ISs, 30%AWB colloids exhibited greater inhibition of Tl(I) migration due to their increased adsorption capacity. Additionally, aging promoted the migration of biochar colloids in the media. Greater biochar aging notably enhanced this promotion, potentially owing to reduced colloidal particle size and the formation of biochar derivatives. Moreover, 50%AWB (biochar aged with 50 % (w/w) HNO3) inhibited Tl(I) migration under low ISs but had almost no impact under high ISs. Nonetheless, at high pH, 50%AWB colloids facilitated Tl(I) migration. This phenomenon might be attributed to the inhibitory effect of aged biochar colloids on Tl(I) adsorption onto media at a high pH, as well as the stable binding between Tl(I) and aged biochar colloids. This study discusses the cotransport of biochar with various degrees of aging and Tl(I) in media, providing insights into remediating soils contaminated with Tl.

Sequestration and oxidation of heavy metals mediated by Mn(II) oxidizing microorganisms in the aquatic environment.

Microorganisms can oxidize Mn(II) to biogenic Mn oxides (BioMnOx), through enzyme-mediated processes and non-enzyme-mediated processes, which are generally considered as the source and sink of heavy metals due to highly reactive to sequestrate and oxidize heavy metals. Hence, the summary of interactions between Mn(II) oxidizing microorganisms (MnOM) and heavy metals is benefit for further work on microbial-mediated self-purification of water bodies. This review comprehensively summarizes the interactions between MnOM and heavy metals. The processes of BioMnOx production by MnOM has been firstly discussed. Moreover, the interactions between BioMnOx and various heavy metals are critically discussed. On the one hand, modes for heavy metals adsorbed on BioMnOx are summarized, such as electrostatic attraction, oxidative precipitation, ion exchange, surface complexation, and autocatalytic oxidation. On the other hand, adsorption and oxidation of representative heavy metals based on BioMnOx/Mn(II) are also discussed. Thirdly, the interactions between MnOM and heavy metals are also focused on. Finally, several perspectives which will contribute to future research are proposed. This review provides insight into the sequestration and oxidation of heavy metals mediated by Mn(II) oxidizing microorganisms. It might be helpful to understand the geochemical fate of heavy metals in the aquatic environment and the process of microbial-mediated water self-purification.

Polystyrene microplastics mediate inflammatory responses in the chicken thymus by Nrf2/NF-κB pathway and trigger autophagy and apoptosis.

Microplastics (MPs) are a hot environmental contaminant now. However, researchers paid little attention to their effects on immune organs such as the thymus. Here, we exposed chickens to a concentration gradient of polystyrene microplastics (PS-MPs) and then followed the decrease in the thymus index. HE staining showed cellular infiltration in the thymus. The assay kit corroborated that PS-MPs impelled oxidative stress in the thymus: increased MDA levels, downregulated antioxidants such as SOD, CAT, and GSH, and significantly undermined total antioxidant capacity. Western blotting and qRT-PCR results showed that Nrf2/NF-κB, Bcl-2/Bax, and AKT signaling pathways were activated in the thymus after exposure to PS-MPs. It stimulated the increased expression of downstream such as IL-1ß, caspase-3, and Beclin1, triggering thymus inflammation, apoptosis, and autophagy. This study provides new insights into the field of microplastic immunotoxicity and highlights potential environmental hazards in poultry farming.

Impact of biochar colloids on thallium(I) transport in water-saturated porous media: Effects of pH and ionic strength.

Understanding the migration behavior of thallium (TI) in subsurface environments is essential for Tl pollution prevention. With the wide production and utilization of biochar, the notable ability of biochar colloids to carry environmental contaminants may make these colloids important for Tl(I) mobility. This study systematically investigated the impact of wood-derived biochar (WB) and corn straw-derived biochar (CB) colloids on Tl(I) transport in water-saturated porous media under different pH (5, 7 and 10) and ionic strengths (ISs) (1, 5 and 50 mM NaNO3). WB colloids improved Tl(I) transport under all IS conditions at pH 7 due to the adsorption capacity of biochar and competition for adsorption sites on the sand surface. However, at IS 50 mM, CB colloids slightly impeded Tl(I) mobility due to the straining. In addition, both WB and CB colloids accelerated Tl(I) mobility under all pH conditions at IS 5 mM. At pH 10, the promotion effect was more obvious due to the deprotonation of O-containing functional groups and higher fluidity of biochar colloids. Furthermore, the two-site nonequilibrium model and two-site kinetic attachment/detachment model suitably described the breakthrough curves (BTCs) of Tl(I) and biochar colloids, respectively. The colloid-facilitated solute transport model could also describe Tl(I) transport influenced by biochar colloids reasonably well. This study provides insight into the migration and fate of Tl(I) in the presence of biochar colloids.

Kinetics and mechanism of Thallium(I) oxidation by Permanganate: Role of bromide.

The oxidation of thallium(I) (Tl (I)) to Tl (III) is referred to as an efficient means for Tl removal. Bromide (Br‾) inevitably occurs in nearly all water sources at concentrations of 0.01-67 mg/L (0.14-960 µM). The effect of Br‾ remains largely unclear but likely of critical importance on the redox fate and thus the removal potential of Tl (I) during typical oxidation treatment processes. Here, we investigate the kinetics and tackle the mechanism of Tl (I) oxidation by permanganate (KMnO4) under the influence of Br‾. The results demonstrated that Br‾ at environmental levels exhibited significant catalytic effect on Tl (I) oxidation kinetics by KMnO4 at acidic pH of 4.0-7.0, while no significant effect of Br‾ was observed for Tl(I) oxidation under alkaline conditions of pH 8.0 and 9.0. It was found that the enhanced oxidation kinetics under acidic conditions was driven by the combined effect of and autocatalysis mediated by MnO2 and a fast oxidation kinetics served by in-situ formed bromine species. Through quantifying the relative contributions of those bromine species to the homogenous oxidation of Tl(I), HOBr, Br2 and Br2O were found to play roles in catalyzing the oxidation of Tl(I) by KMnO4. The results discussed herein highlight the critical role of Br‾ on the Tl(I) complex oxidation process by KMnO4 and may have implications for evaluating the redox cycle and removal potential of Tl in bromide-containing water treatment.

Cotransport of thallium(I) with polystyrene plastic particles in water-saturated porous media.

Exploring the transport behaviors of thallium (Tl) in porous media is crucial for predicting Tl pollution in natural soils and groundwater. In recent years, the misuse of plastics has led to plastic becoming an emerging pollutant in soil. In this work, the effects of plastic particles on Tl(I) transport in water-saturated sand columns were investigated under different ionic strengths (ISs), pH values, and plastic particle sizes. The two-site nonequilibrium model was selected to fit the breakthrough curves (BTCs) of Tl(I). The results demonstrated that nanoplastics (NPs) accelerated Tl(I) transport at pH 7, which might be attributed to the competitive adsorption of NPs and Tl(I) on sand surfaces. However, at pH 5, the deposited NPs might provide more adsorption sites for Tl(I), and thus enhance its retention in the columns. In addition, the "straining" process could intercept microplastics (MPs) with Tl(I) that was attached under unfavorable attachment conditions, which would result in the inhibited mobility of Tl(I). On the other hand, the migration of plastics was restrained to some extent when Tl(I) was present. Overall, the findings from this work provided a new perspective for understanding the transport of Tl(I) and plastics in subsurface environments.

Machine learning in natural and engineered water systems.

Water resources of desired quality and quantity are the foundation for human survival and sustainable development. To better protect the water environment and conserve water resources, efficient water management, purification, and transportation are of critical importance. In recent years, machine learning (ML) has exhibited its practicability, reliability, and high efficiency in numerous applications; furthermore, it has solved conventional and emerging problems in both natural and engineered water systems. For example, ML can predict various water quality indicators in situ and real-time by considering the complex interactions among water-related variables. ML approaches can also solve emerging pollution problems with proven rules or universal mechanisms summarized from the related research. Moreover, by applying image recognition technology to analyze the relationships between image information and physicochemical properties of the research object, ML can effectively identify and characterize specific contaminants. In view of the bright prospects of ML, this review comprehensively summarizes the development of ML applications in natural and engineered water systems. First, the concept and modeling steps of ML are briefly introduced, including data preparation, algorithm selection and model evaluation. In addition, comprehensive applications of ML in recent studies, including predicting water quality, mapping groundwater contaminants, classifying water resources, tracing contaminant sources, and evaluating pollutant toxicity in natural water systems, as well as modeling treatment techniques, assisting characterization analysis, purifying and distributing drinking water, and collecting and treating sewage water in engineered water systems, are summarized. Finally, the advantages and disadvantages of commonly used algorithms are analyzed according to their structures and mechanisms, and recommendations on the selection of ML algorithms for different studies, as well as prospects on the application and development of ML in water science are proposed. This review provides references for solving a wider range of water-related problems and brings further insights into the intelligent development of water science.

Phytoplankton community structure in relation to environmental factors and ecological assessment of water quality in the upper reaches of the Genhe River in the Greater Hinggan Mountains.

Phytoplankton assemblages were investigated in 2015 along the seasonal changes of the Genhe River in the Greater Hinggan Mountains. The survey was performed in June (spring), August (summer), and October (autumn) at nine sampling stations to study the community composition, abundance, and biodiversity. The results showed that 61 species belonging to 16 genera were identified, including Bacillariophyta of 31 species, Dinophyta 2 species, Cyanophyta 2 species, Chlorophyta 20 species, Chrysophyta 2 species, and Cryptophyta 1 species; Besides, Bacillariophyta are dominant species. Shannon-Wiener (H') and Pielou (J') indices indicated that phytoplankton community was stable. And these two indices were significantly lower in summer than in spring and autumn. Phytoplankton abundance and biomass show significant differences in each season. The total phytoplankton abundance (1122.3 × 104 ind/L) and biomass (6.5709 mg/L) in summer are much higher than that in spring and autumn. There were few species and low abundance and biomass in the upper reaches of Genhe River; this fact can be explained by the cold climate in the Greater Higgnan Mountains region. Canonical correspondence analysis (CCA) was used to analyze the data. It revealed that Fe3+, Cu2+, pH, and water temperature (WT) were responsible for most of the variation in space in the phytoplankton community. These environmental parameters play an essential role in the community structure variation of phytoplankton in the upper reaches of Genhe River, the strong association between phytoplankton community structure and ecological factors is varied in each season.