Temporal variations of bacterial and eukaryotic community in coastal waters-implications for aquaculture.

Despite increased attention to the aquaculture environment, there is still a lack of understanding regarding the significance of water quality. To address this knowledge gap, this study utilized high-throughput sequencing of 16S rRNA and 18S rRNA to examine microbial communities (bacteria and eukaryotes) in coastal water over different months through long-term observations. The goal was to explore interaction patterns in the microbial community and identify potential pathogenic bacteria and red tide organisms. The results revealed significant differences in composition, diversity, and richness of bacterial and eukaryotic operational taxonomic units (OTUs) across various months. Principal coordinate analysis (PCoA) demonstrated distinct temporal variations in bacterial and eukaryotic communities, with significant differences (P = 0.001) among four groups: F (January-April), M (May), S (June-September), and T (October-December). Moreover, a strong association was observed between microbial communities and months, with most OTUs showing a distinct temporal preference. The Kruskal-Wallis test (P < 0.05) indicated significant differences in dominant bacterial and eukaryotic taxa among months, with each group exhibiting unique dominant taxa, including potential pathogenic bacteria and red tide organisms. These findings emphasize the importance of monitoring changes in potentially harmful microorganisms in aquaculture. Network analysis highlighted positive correlations between bacteria and eukaryotes, with bacteria playing a key role in network interactions. The key bacterial genera associated with other microorganisms varied significantly (P < 0.05) across different groups. In summary, this study deepens the understanding of aquaculture water quality and offers valuable insights for maintaining healthy aquaculture practices. KEY POINTS: • Bacterial and eukaryotic communities displayed distinct temporal variations. • Different months exhibited unique potential pathogenic bacteria and red tide organisms. • Bacteria are key taxonomic taxa involved in microbial network interactions.

Dual-Parasitic Effect Enables Highly Reversible Zn Metal Anode for Ultralong 25,000 Cycles Aqueous Zinc-Ion Batteries.

The use of electrolyte additives is an efficient approach to mitigating undesirable side reactions and dendrites. However, the existing electrolyte additives do not effectively regulate both the chaotic diffusion of Zn2+ and the decomposition of H2O simultaneously. Herein, a dual-parasitic method is introduced to address the aforementioned issues by incorporating 1-ethyl-3-methylimidazolium trifluoromethanesulfonate ([EMIm]OTf) as cosolvent into the Zn(OTf)2 electrolyte. Specifically, the OTf- anion is parasitic in the solvent sheath of Zn2+ to decrease the number of active H2O. Additionally, the EMIm+ cation can construct an electrostatic shield layer and a hybrid organic/inorganic solid electrolyte interface layer to optimize the deposition behavior of Zn2+. This results in a Zn anode with a reversible cycle life of 3000 h, the longest cycle life of full cells (25,000 cycles), and an extremely high initial capacity (4.5 mA h cm-2), providing a promising electrolyte solution for practical applications of rechargeable aqueous zinc-ion batteries.

Pure Amorphous and Ultrathin Phosphate Layer with Superior Ionic Conduction for Zinc Anode Protection.

Fast and uniform ion transport within the solid electrolyte interphase (SEI) is considered a crucial factor for ensuring the long-term stability of metal electrodes. In this study, we present the fabrication of ultrathin artificial interphases consisting of a zinc phosphate nanofilm with pure amorphous characteristics and a surfactant overlayer. The thickness of the interphases can be precisely controlled within the range of a few tens of nanometers. We explore the impact of artificial SEI structure, including thickness and crystallinity, on its protective capabilities. The pure amorphous phosphate layer with optimized nanoscale thickness is found to provide an abundance of short and isotropic ion migration pathways and a low diffusion energy barrier. These features facilitate rapid and homogeneous Zn2+ transportation, resulting in compact and planar zinc deposition. Meanwhile, the hydrophobic alkyl moieties of the overlayer prevent disassociation of water at the interface. As a result, this nanofilm endures ultralong cycling stability with a low overpotential and enables high Zn plating/stripping reversibility. The Zn||MnO2 full cell shows a stable cycle life for 700 cycles under practical conditions of lean electrolyte, high areal capacity cathode, and limited Zn excess. These findings provide insights into the design and optimization of SEI layers for protection of metal anodes.

Bacterial community in Sinonovacula constricta intestine and its relationship with culture environment.

Although the importance of intestinal microbes to aquaculture animals has been recognized, the intestinal bacteria of Sinonovacula constricta and its culture environment are rarely studied. In this study, high-throughput sequencing was used to explore the intestinal bacterial communities of pond water, sediment, and S. constricta intestine. Significance analysis and principal coordinates analysis (PCoA) showed that there were significant differences in bacterial communities among animals' intestine, pond water, and sediment (p < 0.05). Venn analysis showed that intestinal bacteria shared a considerable number of OTUs (operational taxonomic units) with the sediment and water. SourceTracker analysis suggested that the contribution of sediment to the intestinal bacteria of S. constricta was much larger than that of rearing water. The Kruskal-Wallis test showed that the dominant bacterial taxa differed significantly between animals' intestines and the pond environment, and each of them has a unique bacterial composition. A network diagram indicated the complex positive and negative interactions between intestinal bacteria at the OTU level. Furthermore, BugBase analysis indicated that the bacterial contribution to potential pathogens in the animals' intestines is similar to that in sediments, suggesting that sediment was the main source of potential pathogens in S. constricta intestine. This study provided a theoretical basis for environmental regulation and disease prevention of S. constricta in aquaculture. KEY POINTS: • Culture environment had a significant effect on the intestinal bacterial community in S. constricta. • Sediment was a major source of intestinal bacteria and potentially pathogenic bacteria. • Complex positive and negative interactions existed between intestinal bacteria.

A Chlorine-Based Redox Electrochemical Capacitor.

Electrochemical capacitors are under the spotlight due to their high power density, but they have a low energy density. Redox electrolytes have emerged as a promising approach to design high-energy electrochemical energy storage devices. Herein, a chlorine-based redox electrochemical capacitor is reported in an ionic liquid electrolyte. The commercial activated carbon is employed as the working electrode to render the reversible redox of chloride ions in an ionic liquid, by the restriction of micropores on neutral chlorine. The carbon material can simultaneously provide electrical double-layer capacitance. The effective integration of a chlorine redox reaction and electrical double layer allows for high-energy electrochemical capacitors. By this means, a rechargeable chlorine-based redox electrochemical capacitor with reversible capacity and good rate capability and cycling stability is obtained. This work offers a solution for a new type of high-energy electrochemical capacitors.

In Situ Fabrication of Cuprous Selenide Electrode via Selenization of Copper Current Collector for High-Efficiency Potassium-Ion and Sodium-Ion Storage.

Selenium-based materials are considered as desirable candidates for potassium-ion and sodium-ion storage. Herein, an in situ fabrication method is developed to prepare an integrated cuprous selenide electrode by means of directly chemical selenization of the copper current collector with commercial selenium powder. Interestingly, only the electrolyte of 1 m potassium hexafluorophosphate dissolved in 1,2-dimethoxyethane with higher highest occupied molecular orbital energy and lower desolvation energy facilitates the formation of polyselenide intermediates and the further selenization of the copper current collector. Benefiting from the unique thin-film-like nanosheet morphology and the robust structural stability of the integrated electrode, the volume change and the loss of selenide species could be effectively restrained. Therefore, high performance is achieved in both potassium-ion batteries (462 mA h g-1 at 2 A g-1 for 300 cycles) and sodium-ion batteries (775 mA h g-1 at 2 A g-1 for 4000 cycles). The facile fabrication strategy paves a new direction for the design and preparation of high-performance electrodes.

Self-Assembled FeSe2 Microspheres with High-Rate Capability and Long-Term Stability as Anode Material for Sodium- and Potassium-Ion Batteries.

Sodium- and potassium-ion batteries have attracted intensive attention recently as low-cost alternatives to lithium-ion batteries with naturally abundant resources. However, the large ionic radii of Na+ and K+ render their slow mobility, leading to sluggish diffusion in host materials. Herein, hierarchical FeSe2 microspheres assembled by closely packed nano/microrods are rationally designed and synthesized through a facile solvothermal method. Without carbonaceous material incorporation, the electrode delivers a reversible Na+ storage capacity of 559 mA h g-1 at a current rate of 0.1 A g-1 and a remarkable rate performance with a capacity of 525 mA h g-1 at 20 A g-1 . As for K+ storage, the FeSe2 anode delivers a high reversible capacity of 393 mA h g-1 at 0.4 A g-1 . Even at a high current rate of 5 A g-1 , a discharge capacity of 322 mA h g-1 can be achieved, which is among the best high-rate anodes for K+ storage. The excellent electrochemical performance can be attributed to the favorable morphological structure and the use of an ether-based electrolyte during cycling. Moreover, quantitative study suggests a strong pseudocapacitive contribution, which boosts fast kinetics and interfacial storage.

Co9S8@carbon nanofiber as the high-performance anode for potassium-ion storage.

Thanks to their intrinsic merits of low cost and natural abundance, potassium-ion batteries have drawn intense interest and are regarded as a possible replacement for lithium-ion batteries. The larger radius of potassium, however, provides slow mobility, which normally leads to sluggish diffusion of host materials and eventual expansion of volume, typically resulting in electrode failure. To address these issues, we design and synthesize an effective micro-structure with Co9S8 nanoparticles segregated in carbon fiber utilizing a concise electrospinning process. The anode delivers a high K+ storage capacity of 721 mA h g-1 at 0.1 A g-1 and a remarkable rate performance of 360 mA h g-1 at a high current density of 3 A g-1. A small charge-transfer resistance and a high pseudocapacitive contribution that benefit fast potassium ion migration are indicated by quantitative analysis. The outstanding electrochemical performance can be attributed to the distinct architecture design facilitating high active electrode-electrolyte area and fast kinetics as well as controlled volume expansion.

Boosting potassium-storage performance via the functional design of a heterostructured Bi2S3@RGO composite.

Potassium-ion batteries (PIBs) are considered a promising alternative to lithium-ion batteries (LIBs) for next-generation energy storage due to the abundance and competitive cost of potassium resources. However, the excavation and the development of proper electrodes for PIBs are still confronted with great challenges. Herein, a self-assembled bismuth sulfide microsphere wrapped with reduced graphene oxide was fabricated to form a heterostructured Bi2S3@RGO composite via a visible-light-assisted method and served as the anode for PIBs. The as-prepared Bi2S3@RGO composite presented a high reversible specific capacity of 538 mA h g-1 at 0.2 A g-1 and superior rate capability of 237 mA h g-1 at a high current density of 2 A g-1 after 300 cycles. In particular, the high capacity could be ascribed to the synergistic effect of the conversion and alloying reactions during the electrochemical processes, which was validated by ex situ X-ray diffraction. The fabrication of a unique heterostructure combining the self-assembled Bi2S3 microspheres and flexible RGO boosted the facile charge transfer, leading to the enhanced cyclic stability and rate performance.

In Operando Synchrotron Studies of NH4+ Preintercalated V2O5·nH2O Nanobelts as the Cathode Material for Aqueous Rechargeable Zinc Batteries.

NH4+ preintercalated V2O5·nH2O nanobelts with a large interlayer distance of 10.9 Å were prepared by the hydrothermal method. The material showed a large specific capacity of 391 mA·h·g-1 at the 500 mA·g-1 current density in aqueous rechargeable zinc batteries. In operando synchrotron X-ray diffraction demonstrated that the material experienced reversible solid-solution reaction and two-phase transition during charge-discharge cycling, accompanied by the reversible formation/decomposition of a ZnSO4Zn3(OH)6·5H2O byproduct. In operando X-ray absorption spectroscopy confirmed the reversible reduction/oxidation of V, together with small changes in the VO6 local structure. The formation of byproduct was attributed to the dehydration of [Zn(H2O)6]2+, which concurrently improved the desolvation of [Zn(H2O)6]2+ into Zn2+. Bond valence sum map analysis and electrochemical impedance spectroscopy demonstrated that the byproduct improved the charge transfer kinetics of the electrode. Cyclic voltammetry and galvanostatic intermittent titration technique showed that the electrode reaction was dominated by ionic intercalation where the discharge capacity in the voltage window of 1.4-0.85 V was attributed to the intercalation of [Zn(H2O)6]2+, followed by the intercalation of Zn2+ at 0.85-0.4 V.

In Situ Electrochemical Coating Mechanism of NASICON-Structured AgTi2(PO4)3 for Sodium-Ion Batteries.

The development of high-performance electrode materials is of great significance for the next-generation room-temperature sodium-ion batteries. In this work, a new Na super-ionic conductor (NASICON) negative electrode, AgTi2(PO4)3, is prepared by a facile solid-state reaction and employed as a sodium storage material for the first time. In situ X-ray diffraction during battery operation reveals an electrochemically Ag nanoparticle coating mechanism upon sodiation, facilitating the electron transfer in the complex. In addition, two steps of highly reversible biphasic transformation are observed. As a result, a reversible capacity of 214.9 mA h g-1 can be achieved, corresponding to the insertion/extraction of nearly four sodium ions. The AgTi2(PO4)3 electrode also demonstrates better kinetic properties than the bare NaTi2(PO4)3 material. Such an "in situ" decorating method can open up a new direction for the design of NASICON-structured materials.

Metagenomic Analysis of the Effect of Enteromorpha prolifera Bloom on Microbial Community and Function in Aquaculture Environment.

Enteromorpha prolifera blooms considerably affected coastal environments in recent years. However, the effects of E. prolifera on microbial ecology and function remained unknown. In this study, metagenomic sequencing was used to investigate the effect of E. prolifera bloom on the microbial communities and functional genes in an aquaculture environment. Results showed that E. prolifera bloom could significantly alter the microbial composition and abundance, and heterotrophic bacteria comprised the major groups in the E. prolifera bloom pond, which was dominated by Actinomycetales and Flavobacteriales. The study indicated that viruses played an important role in shaping the microbial community and diversity during E. prolifera bloom. These viruses affected various dominant microbial taxa (such as Rhodobacteraceae, Synechococcus, and Prochlorococcus), which produced an obvious impact on potential nutrient transformation. Functional annotation analysis indicated that E. prolifera bloom would considerably shift the metabolism function by altering the structure and abundance of the microbial community. E. prolifera bloom pond had the low ability of potential metabolic capabilities of nitrogen, sulfur, and phosphate, whereas promoted gene abundance of genetic information processing. These changes in the microbial community and function could produce serious effect on aquaculture ecosystem.

The intestinal bacterial community of healthy and diseased animals and its association with the aquaculture environment.

Although increasing levels of attention have been targeted towards aquaculture-associated bacteria, the bacterial community of animal intestines and its relationship with the aquaculture environment need to be further investigated. In this study, we used high-throughput sequencing to analyze the bacterial community of pond water, sediment, and the intestines of diseased and healthy animals. Our data showed that Proteobacteria, Firmicutes, Cyanobacteria, and Bacteroidetes were the dominant taxa of bacteria across all samples and accounted for more than 90% of the total sequence. Difference analysis and Venn diagrams showed that most of the intestinal bacterial OTUs (operational taxonomic units) of diseased and healthy animals were the same as those of sediment and water, indicating that the aquaculture environment was the main source of intestinal bacteria. Compared with healthy animals, a considerable reduction of OTUs was evident in diseased animals. Welch's t test showed that the dominant bacterial taxa in sediment, water, and animal intestine were significantly different (p < 0.05) and each had its own unique dominant microorganisms. In addition, differences between the intestinal bacteria of healthy and diseased animals were represented by potential probiotics and pathogens, such as Bacillus, Vibrio, Oceanobacillus, and Lactococcus. Principal component analysis (PcoA) showed that a similar environment shaped a similar microbial structure. There was a large difference in the spectrum of intestinal bacteria in diseased animals; furthermore, the spectrum of intestinal bacteria in diseased animals was very different from the environment than in healthy animals. This study provides a theoretical basis for a relationship between the intestinal bacteria of healthy and diseased animals and the environment and provides guidance for environmental regulation and disease prevention in aquaculture areas.

Graphene oxide wrapped Cu3V2O7(OH)2 · 2H2O nanocomposite with enhanced electrochemical performance for lithium-ion storage.

Transition metal oxides (TMOs) are widely accepted as one of the alternatives for the graphite anode in lithium-ion batteries (LIBs) owing to the high specific capacity and facile synthesis of nanoscale materials facilitating fast ionic transfer. However, the lower electronic conductivity always impedes the application of TMOs. Herein, we report a graphene oxide wrapped layer-structured Cu3V2O7(OH)2 · 2H2O nanocomposite (CVO/GO) synthesized via an in situ co-precipitation method. It is corroborated that the introduction of GO not only provides more active sites for lithium-ion storage, but also improves the charge transfer rate of the electrode, issuing an enhanced electrochemical performance. As expected, the CVO/GO nanocomposite exhibits an ultrahigh specific capacity of 870 mA h g-1 at 0.1 A g-1 compared with CVO nanoparticles. Even at a high current density of 5 A g-1, a specific capacity of 158 mA h g-1 could be achieved for the CVO/GO nanocomposite.

Ti3C2T x MXene decorated with Sb nanoparticles as anodes material for sodium-ion batteries.

A large family of two-dimensional (2D) transition metal carbides, MXene, has demonstrated potential applications for electrochemical energy storage. 2D MXene sheets may buffer large volume changes and form a 3D conductive network to facilitate the electronic transfer of working electrodes. However, multilayer Ti3C2T x material could only deliver a moderate capacity in sodium ion battery cells, below the requirement of commercial applications. Herein, we decorated multilayer MXene (Ti3C2T x ) with Sb nanoparticles (NPs) via a facile solution-phase method, in which Sb NPs with a diameter of about 5-10 nm are absorbed on the surface of MXene layers by the electrostatic attraction action. The hybrid material Ti3C2T x @Sb-0.5 delivers a higher reversible capacity of 200 mA h g-1 at 0.1 A g-1 than that of pure Ti3C2T x (90 mA h g-1), and shows a much better capacity retention of nearly 98% after 500 cycles compared with Sb NPs. Also, it achieves superior rate performance (remaining a capacity of 127 mA h g-1 at 2 A g-1) and excellent long-term stability (a capacity retention of almost 92.3% after 8000 cycles). These results indicate that Ti3C2T x @Sb-0.5 possess a potential for high-performance sodium ion batteries anodes.

High Rate Capability and Enhanced Cyclability of Na3 V2 (PO4 )2 F3 Cathode by In†Situ Coating of Carbon Nanofibers for Sodium-Ion Battery Applications.

A facile chemical vapor deposition method is developed for the preparation of carbon nanofiber (CNF) composite Na3 V2 (PO4 )2 F3 @C as cathodes for sodium-ion batteries. In all materials under investigation, the optimized composite content, denoted as NVPF@C@CNF-5, shows excellent sodium storage performance (86.3 % capacity retention over 5000 cycles at 20 C rate) and high rate capability (84.3 mA h g-1 at 50 C). The superior sodium storage performance benefits from the enhanced electrical conductivity of the working electrode after formation of a composite with CNF. Furthermore, the full cell using NVPF@C@CNF-5 and hard carbon as the cathode and anode, respectively, demonstrates an impressive electrochemical performance, realizing an ultrahigh rate charge/discharge at a current rate of 30 C and long-term stability over 1000 cycles. This approach is facile and effective, and could be extended to other materials for energy-storage applications.

Assembly of Na3V2(PO4)2F3@C nanoparticles in reduced graphene oxide enabling superior Na+ storage for symmetric sodium batteries.

Reduced graphene oxide (rGO) was used to encapsulate Na3V2(PO4)2F3@Carbon nanoparticles to overcome its inherent low electronic conductivity and achieve superior sodium storage performance. This as-prepared cathode delivers a remarkable rate performance with a discharge capacity of ca. 64 mA h g-1 at 70C and an ultra-long-term cyclability over 4000 cycles with great capacity retention of 81% at 30C. This excellent performance can be attributed to the favorable combination of fast ionic conductivity of the NASICON structure and the interpenetrating conductive carbon framework; thus bringing a good pseudocapacitive quality to this material. Furthermore, thanks to the good sodium storage properties at low potential, a symmetric full cell can be assembled using Na3V2(PO4)2F3@C@rGO as both cathode and anode. The full cell delivers a high discharge capacity of 53 mA h g-1 at 20C rate, further demonstrating the feasibility of this hybrid material for smart grids.

Self-Assembled CoS Nanoflowers Wrapped in Reduced Graphene Oxides as the High-Performance Anode Materials for Sodium-Ion Batteries.

It remains a big challenge to identify high-performance anode materials to promote practical applications of sodium-ion batteries. Herein, the facile synthesis of CoS nanoflowers wrapped in reduced graphene oxides (RGO) is reported, and their sodium storage properties are systematically studied in comparison with bare CoS. The CoS@RGO nanoflowers deliver a high reversible capacity of 620 mAh g-1 at a current density of 100 mA g-1 and superior rate capability with discharge capacity of 329 mAh g-1 at 4 A g-1 , much higher than those of the bare CoS. Evidenced by electrochemical impedance spectra and ex-situ SEM images, the improvement in the sodium storage performance is found to be due to the introduction of RGO which serves as a conducting matrix, to not only increase the kinetic properties of CoS, but also buffer the volume change and maintain the integrity of working electrodes during (de)sodiation processes. More importantly, the pseudocapacitive contribution of more than 89 % is only observed in the CoS@RGO nanocomposites, owing to the enhanced specific area and surface redox behavior.

Assessment of the effect of Enteromorpha prolifera on bacterial community structures in aquaculture environment.

In recent years, Enteromorpha prolifera blooms had serious impacts on costal environments and fisheries in China. Nevertheless, the effects of E. prolifera on microbial ecology remain unknown. In this study, for the first time, an Illumina sequencing analysis was used to investigate bacterial communities in source water, aquaculture ponds with E. prolifera, and an aquaculture pond in which E. prolifera -free. Principal coordinate and phylogenic analyses revealed obvious differences among the bacterial communities in the pond water with and without E. prolifera. Abundant bacterial taxa in the E. prolifera-containing pond were generally absent from the pond without E. prolifera. Interestingly, pond water with E. prolifera was dominated by Actinomycetales (> 50%), as well as by anaerobic bacteria in the underlying sediment (Desulfobacterales and Desulfuromonadales (> 20%). Pond water in which E. prolifera-free was dominated by Rhodobacterales (58.19%), as well as aerobic and facultative anaerobic bacteria in the sediment. In addition, the ecological functions of other dominant bacteria, such as Candidatus Aquiluna, Microcella spp., and Marivita spp., should be studied in depth. Overall, massive growth of E. prolifera will have serious effects on bacterial communities, and, thus, it will have an important impact on the environment. The novel findings in this study will be valuable for understanding green tides.

Exploration of Spinel LiCrTiO4 as Cathode Material for Rechargeable Mg-Li Hybrid Batteries.

Mg-Li hybrid batteries have attracted wide interest in recent years because of their potential safety as well as their cost benefit and high volumetric capacity. However, slow kinetic properties strongly hinder their commercial application. In this study, we have prepared spinel LiCrTiO4 by a solid-state reaction and have conducted a comprehensive study aimed at improving the performance of Mg-Li hybrid batteries by optimizing the dual-salt electrolyte. LiCrTiO4 has been found to show reversible discharge/charge capacities of 178 and 169 mA h g-1 in electrolytes of 1 m LiCl and 0.3 m APC (all-phenyl-complex), respectively. When the concentration of APC was increased to 0.4 m, LiCrTiO4 showed a high capacity retention of 95 % after 30 cycles. In addition, no phase transition could be observed for an LiCrTiO4 electrode in a dual-salt system, suggesting high electrochemical reversibility. Ex situ EDX and SEM studies have indicated that only Li+ ions are inserted into the cathode side, while Mg2+ ions are reversibly deposited on the surface of Mg metal without dendrite-like growth, indicative of good safety of the Mg-Li hybrid batteries.