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    PoCXCL8, a teleost chemokine, exerts direct bactericidal, chemotactic/ phagocytic, and NETs releasing properties, promoting host anti-bacterial immunity

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    As an important CXC chemokine, CXCL8 plays pleiotropic roles in immunological response. In teleost, CXCL8 is involved in cell migration and bacterial invasion. However, the immune antibacterial function of CXCL8 in Japanese flounder (Paralichthys olivaceus) (PoCXCL8) is largely scarce. In this research, we investigated the antibacterial property and leukocyte activation of PoCXCL8. PoCXCL8 consists of 100 amino acid residues, with a conserved chemokine CXC domain. PoCXCL8 was expressed in various tissues, with the highest level in liver and the lowest level in muscle, and sharply induced by V. harveyi or E. tarda in liver, spleen, and head kidney. In vitro, the recombinant PoCXCL8 (rPoCXCL8) could bind to Bacillus subtilis, Edwardsiella tarda, Escherichia coli, Pseudomonas fluorescens, Vibrio anguillarum, Vibrio harveyi, Staphylococcus aureus, and Micrococcus luteus, affect the growth of E. coli, E. tarda, M. luteus, and P. fluorescens, and have a direct bactericidal effect on E. coli and E. tarda. Moreover, rPoCXCL8 was able to bind the outer membranal protein rPilA of E. tarda. In addition, rPoCXCL8 could bind to PBLs, activating the PBLs activity including chemotaxis, proliferation, phagocytosis, reactive oxygen species, acid phosphatase activity. At same time, rPoCXCL8 could induce neutrophil to generate neutrophil extracellular traps (NETs) and promote the expression of inflammatory genes including IL-1 beta, IL6, MMP13, TNF alpha, and NF-kappa B. In flounder, the presence of rPoCXCL8 could enhance the in vivo resistance to E. tarda in liver, spleen, and head kidney. Moreover, the PoCXCL8-deficient could attenuate the fish defense against E. tarda infection in in spleen and head kidney. In conclusion, these results provided new insights into the antibacterial properties of CXCL8 in P. olivaceus

    Development and application of diffusive gradients in thin-films for in-situ monitoring of 6PPD-Quinone in urban waters

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    The occurrence and risk of N-(1,3-dimethylbutyl)-N '-phenyl-p-phenylenediamine-quinone (6PPD-Q), derived from the oxidation of the tire antidegradant 6PPD, has raised significant concern since it was found to cause acute mortality in coho salmon when exposed to urban runoff. Given the short half-life period and low solubility of 6PPD-Q, reliable in situ measurement techniques are required to accurately understand its occurrence and behaviour in aquatic environments. Here, using the diffusive gradients in thin-films (DGT) method with HLB as a binding agent, we developed a new methodology to measure 6PPD-Q in urban waters. 6PPD-Q was rapidly and strongly adsorbed on the HLB-binding gel and was efficiently extracted using organic solvents. The HLB-DGT accumulated 6PPD-Q linearly for >7 d and its performance was not significantly affected by pH (6.5-8.5), ionic strength (0.0001-0.5 M) or dissolved organic matter (0-20 mg L-1). Field evaluation of the DGT method demonstrated its effectiveness in urban runoff, detecting 6PPD-Q levels of 15.8-39.5 ng L-1 in rivers. In snowmelt, DGT detected 6PPD-Q levels of 210 ng L-1 which is two times higher than the value obtained by grab sampling. 6PPD-Q levels were much higher in snowmelt than those in rivers. This indicates that snowfall constitutes an important transport pathway for 6PPD-Q and that DGT effectively captured the fraction continuously released from dust particles in the snow samples. 6PPD-Q posed a substantial risk to migratory fish in urban waters, and its release from tire wear particles requires further investigation. This study is the first to develop a DGT-based method for 6PPD-Q determination in urban waters, and the method can ensure an accurate measurement of the release of 6PPD-Q to the environment, particularly in rainfall or snowmelt, important pathways for its entry into the aquatic environment

    The response of soil carbon mineralization losses to changes in rainfall frequency is seasonally dependent in an estuarine saltmarsh

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    Altered rainfall distribution patterns resulting from climate change have substantial effects on soil carbon (C) cycling in terrestrial ecosystems particularly in water-limited regions. However, how rainfall redistribution affects soil C mineralization (CO2 and CH4 fluxes) in humid regions such as of the coastal saltmarshes remain unclear. We conducted mesocosm experiments in an estuarine saltmarsh in the Yellow River Delta of China, where we simulated three rainfall frequency scenarios (high-frequency, medium-frequency and low-frequency) with the same total rainfall amount in the dry and wet seasons, respectively. Soil CO2 and CH4 fluxes were measured before and after rain frequency treatment during a 40-day period for each season. The decrease in rainfall frequency significantly reduced the mean soil CO2 and CH4 fluxes during the dry season, but had no effect on either flux during the wet season. The seasonal variation in the response of soil C mineralization to rainfall frequency changes could be explained by the changes in antecedent soil water and salinity conditions, soil C substrate, microbial activities and diversity. Thus, the effects of changes in rainfall frequency on soil C mineralization are regulated by season, and should be considered when predicting the future C balance of coastal wetland ecosystems. Furthermore, the shift in precipitation frequency distribution towards increasing heavy rainfall events during the dry season in this region will have a great effect on soil C losses, potentially feeding back into the soil C budget and stability in this estuarine saltmarsh

    Genomic and single-cell analyses reveal genetic signatures of swimming pattern and diapause strategy in jellyfish

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    Jellyfish exhibit innovative swimming patterns that contribute to exploring the origins of animal locomotion. However, the genetic and cellular basis of these patterns remains unclear. Herein, we generated chromosome-level genome assemblies of two jellyfish species, Turritopsis rubra and Aurelia coerulea, which exhibit straight and free-swimming patterns, respectively. We observe positive selection of numerous genes involved in statolith formation, hair cell ciliogenesis, ciliary motility, and motor neuron function. The lineage-specific absence of otolith morphogenesis- and ciliary movement-related genes in T. rubra may be associated with homeostatic structural statocyst loss and straight swimming pattern. Notably, single-cell transcriptomic analyses covering key developmental stages reveal the enrichment of diapause-related genes in the cyst during reverse development, suggesting that the sustained diapause state favours the development of new polyps under favourable conditions. This study highlights the complex relationship between genetics, locomotion patterns and survival strategies in jellyfish, thereby providing valuable insights into the evolutionary lineages of movement and adaptation in the animal kingdom. Jellyfish represent a critical step in the evolution of early animal movement systems. Here, the authors identify adaptive genetic bases explaining the loss of statocysts in Turritopsis rubra and its ability for reverse development

    Moderate nitrogen enrichment increases CO<sub>2</sub> sink strength in a coastal wetland

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    Coastal wetlands remarkably influence terrestrial carbon (C) stock by serving as natural reservoirs for 'blue carbon'. Anthropogenic nitrogen (N) enrichment shapes the dynamics of soil and plant communities, consequently affecting the C balance and ecosystem functions. The impacts of various levels of N enrichment on CO2 sequestration in coastal wetlands, however, remain elusive. Here we conducted a long-term field study of N fertilization in a coastal wetland in the Yellow River Delta, China, to investigate N effects on soil properties, indicators of plant dynamics, and fluxes of ecosystem CO2. The results indicated that moderate N enrichment (5 g N m(-2) y(-1)) stimulated C fluxes with increases in gross primary productivity (+26.4%), ecosystem respiration (+23.3%), and net ecosystem exchange (NEE, +31.5%) relative to the control. High (10 g N m(-2) y(-1)) and extreme (20 g N m(-2) y(-1)) amounts of N enrichment, however, had relatively minor impacts on these CO2 fluxes. Overall, we observed a decrease in soil electrical conductivity (-24.6%) and increases in soil organic C (+25.2%) and microbial biomass C (+369.3%) for N enrichment. N enrichment also altered the composition of plant species, with a higher proportion of a local dominant species (Phragmites australis), and affected root biomass distribution, with more biomass near the soil surface. Structural equation modeling explained 65.2% of the variance of NEE and supported the assumption that N enrichment could alter the dynamics of soil properties and plant conditions and accelerate ecosystem CO2 sequestration. These findings have important implications for forecasting the C cycle with increasing N deposition in coastal wetlands, contributing to the projections of the global C budget

    Unveiling microplastic's ' s role in nitrogen cycling: Metagenomic insights from estuarine sediment microcosms

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    Marine microplastics (MPs) pollution, with rivers as a major source, leads to MPs accumulation in estuarine sediments, which are also nitrogen cycling hotspots. However, the impact of MPs on nitrogen cycling in estuarine sediments has rarely been documented. In this study, we conducted microcosm experiment to investigate the effects of commonly encountered polyethylene (PE) and polystyrene (PS) MPs, with two MPs concentrations (0.3% and 3% wet sediment weight) based on environmental concentration considerations and dose-response effects, on sediment dissolved oxygen (DO) diffusion capacity and microbial communities using microelectrode system and metagenomic analysis respectively. The results indicated that high concentrations of PE-MPs inhibited DO diffusion during the mid-phase of the experiment, an effect that dissipated in the later stages. Metagenomic analysis revealed that MP treatments reduced the relative abundance of dominant microbial colonies in the sediments. The PCoA results demonstrated that MPs altered the microbial community structure, particularly evident under high concentration PE-MPs treatments. Functional analysis related to the nitrogen cycle suggested that PS-MPs promoted the nitrification, denitrification, and DNRA processes, but inhibited the ANRA process, while PE-MPs had an inhibitory effect on the nitrate reduction process and the ANRA process. Additionally, the high concentration of PE-MPs treatment significantly stimulated the abundance of genus (Bacillus) by 34.1% and genes (lip, pnbA) by 100-187.5% associated with plastic degradation, respectively. Overall, in terms of microbial community structure and the abundance of nitrogen cycling functional genes, PEand PS- MPs exhibit both similarities and differences in their impact on nitrogen cycling. Our findings highlight the complexity of MP effects on nitrogen cycling in estuarine sediments and high concentrations of PE-MP stimulated plastic-degrading genus and genes

    Investigation of the causes and mechanisms of hypoxia in the central Bohai Sea in the summer of 2022

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    The deep-water area in the central Bohai Sea (BS) serves as a spawning ground and nursery for fish, shrimp, and crabs. Frequent hypoxia will affect the ecological environment in the central BS. Data from an on-site investigation of the central BS in the spring and summer of 2022 were used to analyze the relevant factors generating the occurrence of hypoxia in the central BS through the eutrophication index E, apparent oxygen consumption (AOU), and Spearman correlation. The hypoxia area was largely distributed in the study area's deep water section, and stratification was the main cause of hypoxia at the bottom. Organic matter mineralization, degradation, and biological respiration further exacerbated the hypoxia. In the summer of 2022, temperature stratification was the dominant factor influencing hypoxia

    Continuous Field Determination and Ecological Risk Assessment of Pb in the Yellow Sea of China

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    Field determination and ecological risk assessment of dissolved lead (Pb) were performed at two Yellow Sea sites in China using a continuous automated electrochemical system (CAEDS). This CAEDS instrument includes an automatic triple filter sampler and an electrochemical detection water quality analyzer, which might be operated automatically four times daily. The dissolved Pb concentrations varied from 0.29 to 1.57 mu g/L in the South Yellow Sea over 16 days and from 0.32 to 2.28 mu g/L in the North Yellow Sea over 13 days. During the typhoon and algal bloom periods, the Pb concentration was as high as ten times greater than usual. According to the calculation of contamination factors (Cf) and subsequent analysis, seawater quality was classified as Grade II. Through species sensitivity distribution (SSD) method experiments and ecological risk analysis, an average risk quotient (RQ) below 1 for both areas was obtained, indicating a low-to-moderate ecological risk. This system will be helpful for Pb monitoring and assessment in seawater and contribute to the biogeochemical cycling study of Pb

    Synergistic enhancement of oil-water separation and flame retardant properties of melamine sponges based on 9,10-dihydro-9-oxa-10-phospha-phenanthrene-10-oxide (DOPO) and perfluorinated compounds

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    Facing the escalating issue of industrial wastewater discharge and its profound environmental repercussions, the creation of novel sponge materials that excel in oil-water separation while incorporating flame retardancy becomes critically urgent. Despite their superior absorption capabilities, conventional oil-water separation sponges typically overlook flame retardant features, a limitation that curtails their applicability. To address this gap, we have developed a multifunctional hydrophobic sponge through a sophisticated multi-step chemical self-assembly process. This method grafts 9,10-Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and perfluorinated compounds onto melamine foam (MF), yielding a composite material designated as DOPO-PF@MF. DOPOPF@MF boasts a dual functionality of hydrophobicity and flame retardance. Its modified surface exhibits a pronounced hydrophobic-lipophilic balance, with a static water contact angle of 134 degrees. It also displays favorable wetting characteristics towards various organic solvents, such as methanol, ethanol, dimethylformamide, dichloromethane, and hexane. This material demonstrates an impressive adsorption capacity for these solvents, with the adsorption-desorption capacity for ethanol remaining consistent over ten cycles. Furthermore, DOPOPF@MF efficiently separates emulsions of methylene chloride and water, showcasing its versatility. Moreover, DOPO-PF@MF exhibits commendable chemical resilience under extreme temperatures, ranging from 0 degrees C to 100 degrees C, and withstands both acidic and alkaline conditions (pH 1-14), preserving its structural integrity against corrosive substances. Most notably, it surpasses unmodified melamine foam in flame retardancy. The incorporation of DOPO fortifies the material's resistance to high-temperature ignition, effectively inhibiting flame propagation and reducing burn rate, enhancing safety measures

    Synergistic enhancement of oil-water separation and flame retardant properties of melamine sponges based on 9,10-dihydro-9-oxa-10-phospha-phenanthrene-10-oxide (DOPO) and perfluorinated compounds

    No full text
    Facing the escalating issue of industrial wastewater discharge and its profound environmental repercussions, the creation of novel sponge materials that excel in oil-water separation while incorporating flame retardancy becomes critically urgent. Despite their superior absorption capabilities, conventional oil-water separation sponges typically overlook flame retardant features, a limitation that curtails their applicability. To address this gap, we have developed a multifunctional hydrophobic sponge through a sophisticated multi-step chemical self-assembly process. This method grafts 9,10-Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and perfluorinated compounds onto melamine foam (MF), yielding a composite material designated as DOPO-PF@MF. DOPOPF@MF boasts a dual functionality of hydrophobicity and flame retardance. Its modified surface exhibits a pronounced hydrophobic-lipophilic balance, with a static water contact angle of 134 degrees. It also displays favorable wetting characteristics towards various organic solvents, such as methanol, ethanol, dimethylformamide, dichloromethane, and hexane. This material demonstrates an impressive adsorption capacity for these solvents, with the adsorption-desorption capacity for ethanol remaining consistent over ten cycles. Furthermore, DOPOPF@MF efficiently separates emulsions of methylene chloride and water, showcasing its versatility. Moreover, DOPO-PF@MF exhibits commendable chemical resilience under extreme temperatures, ranging from 0 degrees C to 100 degrees C, and withstands both acidic and alkaline conditions (pH 1-14), preserving its structural integrity against corrosive substances. Most notably, it surpasses unmodified melamine foam in flame retardancy. The incorporation of DOPO fortifies the material's resistance to high-temperature ignition, effectively inhibiting flame propagation and reducing burn rate, enhancing safety measures

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