FAM111A induces nuclear dysfunction in disease and viral restriction.

Mutations in the nuclear trypsin-like serine protease FAM111A cause Kenny-Caffey syndrome (KCS2) with hypoparathyroidism and skeletal dysplasia or perinatally lethal osteocraniostenosis (OCS). In addition, FAM111A was identified as a restriction factor for certain host range mutants of the SV40 polyomavirus and VACV orthopoxvirus. However, because FAM111A function is poorly characterized, its roles in restricting viral replication and the etiology of KCS2 and OCS remain undefined. We find that FAM111A KCS2 and OCS patient mutants are hyperactive and cytotoxic, inducing apoptosis-like phenotypes such as disruption of nuclear structure and pore distribution, in a protease-dependent manner. Moreover, wild-type FAM111A activity causes similar nuclear phenotypes, including the loss of nuclear barrier function, when SV40 host range mutants attempt to replicate in restrictive cells. Interestingly, pan-caspase inhibitors do not block these FAM111A-induced phenotypes, implying it acts independently or upstream of caspases. In this regard, we identify nucleoporins and the associated GANP transcription/replication factor as FAM111A interactors and candidate targets. Overall, we reveal a potentially unifying mechanism through which deregulated FAM111A activity restricts viral replication and causes KCS2 and OCS.

A meta-analysis reveals that geographical factors drive the bacterial community variation in Chinese lakes.

The biogeographical distribution of plants and animals has been extensively studied, however, the biogeographical patterns and the factors that influence bacterial communities in lakes over large scales are yet to be fully understood, even though they play critical roles in biogeochemical cycles. Here, bacterial community compositional data, geographic information, and environmental factors were integrated for 326 Chinese lakes based on previously published studies to determine the underlying factors that shape bacterial diversity among Chinese lakes. The composition of bacterial communities significantly varied among the three primary climatic regions of China (Northern China, NC; Southern China, SC; and the Tibetan Plateau, TIP), and across two different lake habitats (waters and sediments). Sediment bacterial communities exhibited significantly higher alpha-diversity and distance-decay relationships compared to water communities. The results indicate that the "scale-dependent patterns" of controlling factors, primarily influenced by geographical factors, become increasingly pronounced as the spatial scale increases. At a national scale, geographical factors exerted a dominant influence on both the water and sediment communities across all lakes, as geographical barriers restrict the dispersal of individuals. At smaller spatial scales, temperature-driven selection effects played a greater role in shaping water bacterial community variation in the NC, SC, and TIP, while geographical factors had a stronger association with sediment bacterial community variation in the lakes of the three regions. This synthesis offers novel insights into the ecological factors that determine the distribution of bacteria in Chinese lakes.

Minute Cu2+ coupling with HCO3- for efficient degradation of acetaminophen via H2O2 activation.

Homogeneous Cu2+-mediated activation of H2O2 has been widely applied for the removal of organic contaminants, but fairly high dosage of Cu2+ is generally required and may cause secondary pollution. In the present study, minute Cu2+ (2.5 µM) catalyzed H2O2 exhibited excellent efficiency in degradation of organic pollutants with the assistant of naturally occurring level HCO3- (1 mM). In a typical case, acetaminophen (ACE) was completely eliminated within 10 min which followed the pseudo-first-order kinetics. Singlet oxygen and superoxide radical rather than traditionally identified hydroxyl radical were the predominant reactive oxygen species (ROS) responsible for ACE degradation. Meanwhile, Cu3+ was deduced through Cu+ and p-hydroxybenzoic acid formation analysis. CuCO3(aq) was the main complex with high reactivity for the activation of H2O2 to form ROS and Cu3+. The removal efficiency of ACE depended on the operating parameters, such as Cu2+, HCO3- and H2O2 dosage, solution initial pH. The presence of Cl-, HPO42-, humic acid were found to retard ACE removal while other anions such as SO42- and NO3- had no obvious effect. ACE exhibited lower degradation efficiency in real water matrices than that in ultra-pure water. Nevertheless, 58-100% of ACE was removed from domestic wastewater, lake water and tap water within 60 min. Moreover, eight intermediate products were identified and the possible degradation pathways of ACE were proposed. Additionally, other typical organic pollutants including bisphenol A, norfloxacin, lomefloxacin hydrochloride and sulfadiazine, exhibited great removal efficiency in the Cu2+/H2O2/HCO3- system.

The partitioning behavior of PAHs between settled dust and its extracted water phase: Coefficients and effects of the fluorescent organic matter.

The occurrence and distribution of polycyclic aromatic hydrocarbons (PAHs) in a city of Central China were determined in the settled dust and its extracted water phase from different land use types and bus stops in Nanchang City. The physicochemical properties of its water extracted dissolved organic matter (WEOM) were characterized to investigate the effect of fluorescence organic matter on the dust-water partitioning coefficients (Kd) using three-dimensional excitation-emission matrix fluorescence spectroscopy combined parallel factor analysis. Results showed that the range of ∑PAHs in settled dust and the extracted water phase was 0.05-15.92 µg·g-1 and 2-211 ng·L-1, respectively. These PAHs mostly came from the combustion of biomass. The risk assessment showed that PAHs in dust had no obvious health risk (less than the magnitude of 10-6). Additionally, the high molecular weight (HMW) PAHs and the low molecular weight (LMW) PAHs were preferentially adsorbed by dust and the dissolved portion, respectively. It was confirmed by the relatively high logKd values of 4.23 for the HMW-PAHs. Pearson correlation analysis suggested that the higher concentration of dissolved organic carbon and humic-like substance were in favor of PAHs in dust released into waters. This study can provide information on pollution control when considering the impact of fluorescent organic matter on the fate and transport of PAHs.

Exploration of the variations and relationships between trace metal enrichment in dust and ecological risks associated with rapid urban expansion.

Trace metals in street dust originate from many natural and anthropogenic sources and may directly or indirectly affect daily life and health. Here, the enrichment factor (EF), an efficient parameter to assess the contamination by trace metals, was evaluated and compared in four different zones of the urban area of Nanchang city during different seasons. Results showed that EFs of trace metals have regional seasonal variations. The EF range of Cr, Ni, Cu, Zn, As, Cd and Pb were found to be (0.76-16.38), (0.66-9.06), (1.09-169.58), (1.52-36.16), (0.44-7.17), (2.07-78.38), (0.95-20.94), respectively. These values indicate minimal to significant pollution. The EF values of Zn, Cd and Pb in street dust show very similar variations as their median and mean values of EF are higher in certain zones, and their seasonal variations are similar. The Ni and As results suggest that anthropogenic influences for these elements are not significant. The Ni may be influenced by land use type rather than point sources and As may be attributed to natural sources. The Principal Component Absolute Scores - Multivariate Linear Regression (PCAS-MLR) model was used to identify the types and contributions of trace metal sources. The main sources of trace metals in dust were found to be industrial discharges and traffic emissions. However, the percentages of their contributions have significant regional differences. The relationship between the EF of trace metals and the ecological risk index (ERI) was also investigated, and indicates that seriously polluted areas correspond to high ERI regions. The land use types and characteristics of the source jointly affects the relationship between EFs and ERI.

SUMO-targeted ubiquitin ligase activity can either suppress or promote genome instability, depending on the nature of the DNA lesion.

The posttranslational modifiers SUMO and ubiquitin critically regulate the DNA damage response (DDR). Important crosstalk between these modifiers at DNA lesions is mediated by the SUMO-targeted ubiquitin ligase (STUbL), which ubiquitinates SUMO chains to generate SUMO-ubiquitin hybrids. These SUMO-ubiquitin hybrids attract DDR proteins able to bind both modifiers, and/or are degraded at the proteasome. Despite these insights, specific roles for SUMO chains and STUbL in the DDR remain poorly defined. Notably, fission yeast defective in SUMO chain formation exhibit near wild-type resistance to genotoxins and moreover, have a greatly reduced dependency on STUbL activity for DNA repair. Based on these and other data, we propose that a critical role of STUbL is to antagonize DDR-inhibitory SUMO chain formation at DNA lesions. In this regard, we identify a SUMO-binding Swi2/Snf2 translocase called Rrp2 (ScUls1) as a mediator of the DDR defects in STUbL mutant cells. Therefore, in support of our proposal, SUMO chains attract activities that can antagonize STUbL and other DNA repair factors. Finally, we find that Taz1TRF1/TRF2-deficiency triggers extensive telomeric poly-SUMOylation. In this setting STUbL, together with its cofactor Cdc48p97, actually promotes genomic instability caused by the aberrant processing of taz1Δ telomeres by DNA repair factors. In summary, depending on the nature of the initiating DNA lesion, STUbL activity can either be beneficial or harmful.

Functional Crosstalk between the PP2A and SUMO Pathways Revealed by Analysis of STUbL Suppressor, razor 1-1.

Posttranslational modifications (PTMs) provide dynamic regulation of the cellular proteome, which is critical for both normal cell growth and for orchestrating rapid responses to environmental stresses, e.g. genotoxins. Key PTMs include ubiquitin, the Small Ubiquitin-like MOdifier SUMO, and phosphorylation. Recently, SUMO-targeted ubiquitin ligases (STUbLs) were found to integrate signaling through the SUMO and ubiquitin pathways. In general, STUbLs are recruited to target proteins decorated with poly-SUMO chains to ubiquitinate them and drive either their extraction from protein complexes, and/or their degradation at the proteasome. In fission yeast, reducing or preventing the formation of SUMO chains can circumvent the essential and DNA damage response functions of STUbL. This result indicates that whilst some STUbL "targets" have been identified, the crucial function of STUbL is to antagonize SUMO chain formation. Herein, by screening for additional STUbL suppressors, we reveal crosstalk between the serine/threonine phosphatase PP2A-Pab1B55 and the SUMO pathway. A hypomorphic Pab1B55 mutant not only suppresses STUbL dysfunction, but also mitigates the phenotypes associated with deletion of the SUMO protease Ulp2, or mutation of the STUbL cofactor Rad60. Together, our results reveal a novel role for PP2A-Pab1B55 in modulating SUMO pathway output, acting in parallel to known critical regulators of SUMOylation homeostasis. Given the broad evolutionary functional conservation of the PP2A and SUMO pathways, our results could be relevant to the ongoing attempts to therapeutically target these factors.

Pli1(PIAS1) SUMO ligase protected by the nuclear pore-associated SUMO protease Ulp1SENP1/2.

Covalent modification of the proteome by SUMO is critical for genetic stability and cell growth. Equally crucial to these processes is the removal of SUMO from its targets by the Ulp1 (HuSENP1/2) family of SUMO proteases. Ulp1 activity is normally spatially restricted, because it is localized to the nuclear periphery via interactions with the nuclear pore. Delocalization of Ulp1 causes DNA damage and cell cycle defects, phenotypes thought to be caused by inappropriate desumoylation of nucleoplasmic targets that are normally spatially protected from Ulp1. Here, we define a novel consequence of Ulp1 deregulation, with a major impact on SUMO pathway function. In fission yeast lacking Nup132 (Sc/HuNUP133), Ulp1 is delocalized and can no longer antagonize sumoylation of the PIAS family SUMO E3 ligase, Pli1. Consequently, SUMO chain-modified Pli1 is targeted for proteasomal degradation by the concerted action of a SUMO-targeted ubiquitin ligase (STUbL) and Cdc48-Ufd1-Npl4. Pli1 degradation causes the profound SUMO pathway defects and associated centromere dysfunction in cells lacking Nup132. Thus, perhaps counterintuitively, Ulp1-mediated desumoylation can promote SUMO modification by stabilizing a SUMO E3 ligase.

RNF4 interacts with both SUMO and nucleosomes to promote the DNA damage response.

The post-translational modification of DNA repair and checkpoint proteins by ubiquitin and small ubiquitin-like modifier (SUMO) critically orchestrates the DNA damage response (DDR). The ubiquitin ligase RNF4 integrates signaling by SUMO and ubiquitin, through its selective recognition and ubiquitination of SUMO-modified proteins. Here, we define a key new determinant for target discrimination by RNF4, in addition to interaction with SUMO. We identify a nucleosome-targeting motif within the RNF4 RING domain that can bind DNA and thereby enables RNF4 to selectively ubiquitinate nucleosomal histones. Furthermore, RNF4 nucleosome-targeting is crucially required for the repair of TRF2-depleted dysfunctional telomeres by 53BP1-mediated non-homologous end joining.

Hypochlorite-mediated degradation and detoxification of sulfathiazole in aqueous solution and soil slurry.

Although various activated sodium hypochlorite (NaClO) systems were proven to be promising strategies for recalcitrant organics treatment, the direct interaction between NaClO and pollutants without explicit activation is quite limited. In this work, a revolutionary approach to degrade sulfathiazole (STZ) in aqueous and soil slurry by single NaClO without any activator was proposed. The results demonstrated that 100% and 94.11% of STZ could be degraded by 0.025 mM and 5 mM NaClO in water and soil slurry, respectively. The elimination of STZ was shown to involve superoxide anion (O2•-), chlorine oxygen radical (ClO•), and hydroxyl radical (•OH), according to quenching experiments and the analysis of electron paramagnetic resonance. The addition of Cl-, HCO3-, SO42-, and humic acid (HA) marginally impeded the decomposition of STZ, while NO3-, Fe3+, and Mn2+ facilitated the process. The NaClO process exhibited significant removal effectiveness at a neutral initial pH. Moreover, the NaClO facilitated application in various soil samples and water matrices, and the procedure was also successful in effectively eliminating a range of sulfonamides. The suggested NaClO degradation mechanism of STZ was based on the observed intermediates, and the majority of the products exhibited lower ecotoxicity than STZ. Besides, the experiment results by using X-ray diffraction (XRD) and a fourier transform infrared spectrometer (FTIR) indicated the negligible effects on the composition and structure of soil by the treatment of NaClO. Simultaneously, the experimental results also illustrated that the bioavailability of heavy metals and the physiochemical characteristics of the soil before and after the remediation did not change to a significant extent. Following the remediation of NaClO, the phytotoxicity tests showed reduced toxicity to wheat and cucumber seeds. As a result, treating soil and water contaminated with STZ by using NaClO was a reasonably practical and eco-friendly method.

Effect of pyrolysis temperature and molecular weight on characterization of biochar derived dissolved organic matter from invasive plant and binding behavior with the selected pharmaceuticals.

A comprehensive understanding of the characteristics of biochar released-dissolved organic matter (BDOM) derived from an invasive plant and its impact on the binding behavior of pharmaceuticals is essential for the application of biochar, yet has received less attention. In this study, the binding behavior of BDOM pyrolyzed at 300-700 °C with sulfathiazole, acetaminophen, chloramphenicol (CAP), and carbamazepine (CMZ) was investigated based on a multi-analytical approach. Generally, the pyrolysis temperature exhibited a more significant impact on the spectral properties of BDOM and pharmaceutical binding behavior than those of the molecular weight. With increased pyrolysis temperature, the dissolved organic carbon decreased while the proportion of the protein-like substance increased. The highest binding capacity towards the drugs was observed for the BDOM pyrolyzed at 500 °C with the molecular weight larger than 0.3 kDa. Moreover, the protein-like substance exhibited higher susceptive and released preferentially during the dialysis process and also showed more sensitivity and bound precedingly with the pharmaceuticals. The active binding points were the aliphatic C-OH, amide II N-H, carboxyl CO, and phenolic-OH on the tryptophan-like substance. Furthermore, the binding affinity of the BDOM pyrolyzed at 500 °C was relatively high with the stability constant (logKM) of 4.51 ± 0.52.

Dual recruitment of Cdc48 (p97)-Ufd1-Npl4 ubiquitin-selective segregase by small ubiquitin-like modifier protein (SUMO) and ubiquitin in SUMO-targeted ubiquitin ligase-mediated genome stability functions.

Protein modification by SUMO and ubiquitin critically impacts genome stability via effectors that "read" their signals using SUMO interaction motifs or ubiquitin binding domains, respectively. A novel mixed SUMO and ubiquitin signal is generated by the SUMO-targeted ubiquitin ligase (STUbL), which ubiquitylates SUMO conjugates. Herein, we determine that the "ubiquitin-selective" segregase Cdc48-Ufd1-Npl4 also binds SUMO via a SUMO interaction motif in Ufd1 and can thus act as a selective receptor for STUbL targets. Indeed, we define key cooperative DNA repair functions for Cdc48-Ufd1-Npl4 and STUbL, thereby revealing a new signaling mechanism involving dual recruitment by SUMO and ubiquitin for Cdc48-Ufd1-Npl4 functions in maintaining genome stability.

Spectral characteristic of the waters with different sizes of particles: impact of water quality and land-use type.

Natural colloids (NCs) are heterogeneous mixtures of particles in the aquatic environments that are strongly influenced by land use and water quality between terrestrial and aquatic environments. However, the relevant study paid little attention to the difference among the waters with different sizes of particles (e.g., suspended particulate matter (SPM), NCs, and the truly soluble substances). In this study, the spectral properties of these different waters were investigated from different land-use types in the Yuan River basin, China. Results of the UV-visible absorption spectral showed that with the particle size increased, the aromaticity, chromophoric dissolved organic matter, and humification degree of organic matter increased, while the condensation degree decreased. Data analysis from the fluorescence indices indicated that the source and the autochthonous feature of the truly soluble substances differed from that of NCs and SPM, whereas the protein-like component was mainly combined with the relatively larger size of particles (i.e., SPM and NCs), especially the downstream. Although the spectral characteristics of the water samples were strongly influenced by the water quality (> 45%), the land-use type might be the real potential impactor. Furthermore, the influence of land-use type on the spectral properties differed between the large and small scale of the buffer strips and between the mainstream and the tributaries. And this effect was more significant on the fluorescence properties in the mainstream and the spectral properties for NCs than for SPM. The study helps to understand the biogeochemical effects of the waters with different particle sizes.

Characterization of copper binding to biochar-derived dissolved organic matter: Effects of pyrolysis temperature and natural wetland plants.

Characterization of the biochar-derived dissolved organic matter (BDOM) is essential to understanding the environmental efficacy of biochar and the behavior of heavy metals. In this study, the binding properties of BDOM derived from different pyrolysis temperatures, wetland plants, and plant organs with Cu was investigated based on a multi-analytical approach. In general, the pyrolysis temperature exhibited a more significant impact on both the spectral characteristics of BDOM and Cu binding behavior than those of the feedstocks. With the pyrolysis temperature increased, the dissolved organic carbon, aromaticity, and fluorescence substance of BDOM decreased and the structure became more condensed. Humic-and tryptophan-like substance was more susceptible to the addition of Cu for BDOM pyrolyzed at 300 â„ƒ and 500 â„ƒ, respectively. In addition, the more tyrosine-like substance is involved in Cu binding at higher pyrolysis temperature (500 â„ƒ). However, the fluvic-like substance occurred preferentially with Cu than the other fluorophores. Moreover, the higher binding capacity for Cu was exhibited by the humic-like substance and by BDOM derived from the higher pyrolysis temperature and the lower elevation plants with the corresponding average stability constants (log KM) of 5.58, 5.36, and 5.16.

Potential of granular complexes of lime and montmorillonite for stabilizing soil cadmium and the underlying mechanisms.

Cadmium (Cd) contaminated soils were widely remediated by alkaline materials in powder, while the effects of granular materials are still unknown. This study was conducted to prepare granular materials based on hydrated lime and montmorillonite with ratios of 1:1, 1:2, and 1:3 (LM1, LM2, and LM3); their effects and mechanisms on stabilizing Cd in hydroponic, pot, and field conditions were further explored. The results showed that powdery materials caused intense pH elevations within 30-60 min and dissolved-Cd reductions within 8-100 min. However, granular materials significantly delayed these effects; the highest solution pH and lowest dissolved-Cd occurred after 250 min. The LM1 granules induced a much higher reduction of dissolved-Cd (99.8%) than that in the LM2 (53.6%) and LM3 granules (14.3%) due to the generation of more cadmium carbonate precipitates. Additionally, the soil pH gradually decreased after an intense elevation induced by powdery materials, but the LM1 granules maintained the soil pH at approximately 7.0, resulting in a lower level of CaCl2-extractable Cd (0.03 mg kg-1) than the LM1 powder (0.22 mg kg-1) after 30 d of cultivation. Similar to lime powder, a small spatial variation (Std. of 3.45) of DGT (diffusive gradient in thin films) extractable Cd in soil profile was observed in the LM1 granules, revealing a homogeneous stabilization effect induced by the LM1 granules. Accordingly, the LM1 granules induced a higher reduction in brown rice Cd (50.9%) than that in the LM1 powders (35.1%). Thus, the granular material of hydrated lime and montmorillonite (1:1) h the potential to replace lime powder in the remediation of Cd-contaminated field.

[Bacterioplankton Communities and Assembly Mechanisms in Wet Season of Lakes, Nanchang].

Bacterioplankton communities play an important role in nutrient cycling and organic matter decomposition in urban lakes. Based on high-throughput sequencing, we analyzed the temporal (April, June, and August) and urban-suburban difference and assembly of bacterioplankton communities in lakes of Nanchang City. Our results showed that:① the dominant bacterioplankton communities in the lakes were Actinobacteria (41.60%), Proteobacteria (22.29%), Cyanobacteria (16.21%), and Bacteroidota (10.17%). ② There were significant differences in bacterial communities between April, June, and August but not between urban lakes and suburban lakes. The abundance of 10 bacteria, mainly Proteobacteria (April>June>August) and Cyanobacteria (June>August>April), was significantly different among the three months. There was a significant distance decay pattern in June, which was not seen in April and August. ③ The proportion of non-freshwater bacteria was significantly higher in June than that in April and August, but there were no significant differences between urban lakes and suburban lakes. ④ Deterministic processes dominated the assembly of bacterioplankton communities, whereas stochastic processes had a lower contribution. Water temperature (WT) was the environmental factor that best explained the changes in bacterioplankton communities in the lakes.

[Characteristics of Microplastic-derived Dissolved Organic Matter(MPDOM) and the Complexation Between MPDOM and Sulfadiazine/Cu2].

Microplastic-derived dissolved organic matter(MPDOM) during the aging process could be complexed with organic pollutants, heavy metals, and other contaminants and thus affect their migration and transformation. In this study, two types of microplastics, polyethylene terephthalate(PET) and polystyrene(PS), were selected to investigate the spectral properties of MPDOM and their effect on the complexation between MPDOM and sulfadiazine(SDZ)/copper ion(Cu2+) using the fluorescence quenching method, various spectroscopic analysis techniques, and the Ryan-Weber quenching model. The results of UV-vis absorption spectroscopy analysis showed that the molecular weight of the two MPDOMs decreased; the aromaticity and humification increased; and the carboxyl, carbonyl, hydroxyl, and ester substituents on aromatic rings increased after aging. The fluorescence quenching process between MPDOM and SDZ/Cu2+ was static quenching. After quenching, the aromaticity and humification of the two MPDOMs were similar, and the molecular weights were comparable. Combined with three-dimensional fluorescence spectra and parallel factor analysis, two humic-like components and one protein-like component were identified. In addition, the protein-like components of MPDOM reacted preferentially with SDZ and were more sensitive to Cu2+. The results of the Ryan-Weber quenching model revealed that the binding ability of humic-like components to PET-DOM was higher in both SDZ and Cu2+ quenching systems, but the binding ability of MPDOM in the SDZ quenching system was generally stronger than that in the Cu2+ system.

[Community Composition, Symbiotic Patterns, and Influencing Factors of Planktonic Fungi in Urban Lakes of Nanchang].

To investigate the characteristics of planktonic fungal communities in Nanchang lakes and the mechanism of environmental stress on planktonic fungal communities, surface water samples were collected from seven major urban lakes evenly distributed in different county-level districts of Nanchang in the dry (February and December), normal (April and October), and wet (June and August) seasons, respectively. The environmental stressors such as WT, DO, NH4+-N, and NO3--N were measured; the characteristics of planktonic fungal communities were studied using high-throughput sequencing; the symbiotic patterns of planktonic fungal communities were elucidated using network analysis and other methods; and the environmental stressors affecting the structure and symbiotic patterns of planktonic fungal communities were revealed. The results showed that ① the planktonic fungal community composition in lakes of Nanchang varied significantly among seasons but not significantly among the lakes. WT, DO, pH, and NH4+-N were the significant environmental stressors affecting the planktonic fungal community composition. ② The dominant phyla of the planktonic fungal community were Chytridiomycota (9.55%-33.14%), Basidiomycota (0.48%-4.25%), and Ascomycota (1.29%-3.19%), and the sizes of the dominant phyla were in the following order:wet season>normal season>dry season. The relative abundance of Chytridiomycota was significantly higher in the wet season than that in the normal season and the dry season, the relative abundance of Basidiomycota was significantly lower in the dry season than that in the normal and wet seasons, and the difference in Ascomycota among seasons was not significant. ③ The stability size of the planktonic fungal community symbiosis network in lakes of Nanchang was in the following order:wet season>normal season>dry season. WT was the best environmental stressor affecting the planktonic fungal community symbiosis pattern. The study can provide theoretical basis for the comprehensive evaluation and management study of the lake and provide guidance for protecting the lake ecosystem in the middle and lower reaches of the Yangtze River.

[Influence of Land Use Structure and Spatial Pattern on Water Quality of Small and Medium-sized Rivers in Poyang Lake Basin].

To reveal the influence mechanism of land use structure and spatial pattern on water quality of small and medium-sized rivers, water samples were collected from 25 sampling points in three small and medium-sized rivers of the Poyang Lake Basin in January 2022 and July 2022. Bioenv analysis, the Mantel test, and variance partitioning analysis were used to quantify the effects of land use structure and spatial patterns on water quality at different spatial scales; generalized additive models were used to fit the relationship between water quality and different land use structures and spatial patterns; and a generalized linear model was used to construct segmented regression models and calculate the thresholds based on the stepwise recursive method. The results showed that:① the average interpretation rate of land use structure and spatial pattern on river water quality was 59.72% during the wet period and 48.95% during the dry period. The sub-basin and riparian 100 m scales were the key scales of land use structure and spatial pattern affecting water quality in small and medium-sized rivers, with an average explanation rate of 54.70% and 64.88%, respectively. The joint explanation of land use structure and spatial pattern was an important factor driving the change in river water quality, accounting for 66.90% of the total explanation. ② The impact of land use structure on the water quality of small and medium-sized rivers had a significant threshold effect. When the proportion of construction land was less than 2%, farmland was less than 8%, or forest land was more than 82% at the sub-basin scale and the proportion of construction land was less than 12%, farmland was less than 41%, or forest land was more than 49% at the riparian buffer scale, all could significantly improve water quality. ③ The effect of spatial pattern on water quality in small and medium-sized rivers also had a threshold effect but was weaker than that of land use structure. A patch shape value more than 28.77 or patch diversity more than 0.69 at the sub-basin scale and a patch shape value more than 2.99 or patch diversity more than 1.02 at the riparian buffer scale could improve water quality. The above results showed that strengthening the management of land use at the sub-basin and riparian 100 m scales and setting a reasonable threshold of land use structure and spatial pattern can effectively prevent water quality from deteriorating.

[Bisulfite Promoted Minute Fe2+-Activated Peroxydisulfate for Paracetamol Degradation].

Fe2+ has been commonly selected to activate peroxydisulfate(PDS) for sulfate radical(SO4-·) generation because of its eco-friendly, cost-effective, and high activity characteristics. However, Fe2+ can be rapidly oxidized to Fe3+ in the reaction, leading to poor utilization of iron for PDS activation. Further, a fairly high concentration of Fe2+ is generally required and may cause iron sludge production and secondary pollution. In this study, a minute Fe2+-activated PDS system induced by bisulfite(BS) was used to degrade paracetamol(APAP) in water. The results showed that the Fe2+-PDS system could be enhanced by the circulation of Fe2+-Fe3+ with the injection of BS and by keeping Fe2+ at a high concentration. Under the optimal conditions(PDS=0.6 mol·L-1; BS=0.4 mol·L-1; Fe2+=10 µmol·L-1; pH=4), 100% APAP(4 µmol·L-1) was removed within 180 s. The degradation rate of APAP increased with the increase in BS(0-0.6 mmol·L-1) and PDS(0.2-1.5 mmol·L-1) concentration, and a modest Fe2+ concentration could accelerate APAP removal. Co-existing substances inhibited the APAP removal and followed the order of HCO3->HPO42->Cl->NO3->humic acid(HA). Based on the quenching experiments and electron paramagnetic resonance spectroscopy test, SO4-· was shown to be the primary reactive species for APAP decomposition in the BS-Fe2+-PDS process. Three-dimensional fluorescence spectroscopy revealed that APAP intermediates had fluorescence characteristics. Moreover, five intermediates were identified, and the probable APAP degradation pathways were proposed. The removal efficiencies of APAP were lower in real waters than that in ultrapure water. Nevertheless, the removal effect was greatly improved after a prolonged reaction time. All results indicated that the BS-Fe2+-PDS system could be a promising method for organic pollutant treatment.