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Vinylene‐linked two‐dimensional polymers (V‐2DPs) and their layer‐stacked covalent organic frameworks (V‐2D COFs) featuring high in‐plane π‐conjugation and robust frameworks have emerged as promising candidates for energy‐related applications. However, current synthetic approaches are restricted to producing V‐2D COF powders that lack processability, impeding their integration into devices, particularly within membrane technologies reliant upon thin films. Herein, we report the novel on‐water surface synthesis of vinylene‐linked cationic 2DPs films (V‐C2DP‐1 and V‐C2DP‐2) via Knoevenagel polycondensation, which serve as the anion‐selective electrode coating for highly‐reversible and durable zinc‐based dual‐ion batteries (ZDIBs). Model reactions and theoretical modeling revealed the enhanced reactivity and reversibility of the Knoevenagel reaction on the water surface. On this basis, we demonstrated the on‐water surface 2D polycondensation towards V‐C2DPs films that show large lateral size, tunable thickness, and high chemical stability. Representatively, V‐C2DP‐1 presents as a fully crystalline and face‐on oriented film with in‐plane lattice parameters of a=b≈43.3 Å. Profiting from its well‐defined cationic sites, oriented 1D channels, and stable frameworks, V‐C2DP‐1 film possesses superior bis(trifluoromethanesulfonyl)imide anion (TFSI−)‐transport selectivity (transference, t_=0.85) for graphite cathode in high‐voltage ZDIBs, thus triggering additional TFSI−‐intercalation stage and promoting its specific capacity (from ~83 to 124 mAh g−1) and cycling life (>1000 cycles, 95 % capacity retention). [ABSTRACT FROM AUTHOR]

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In this paper, we consider a fully nonlinear curvature flow of a convex hypersurface in the Euclidean 𝑛-space. This flow involves 𝑘-th elementary symmetric function for principal curvature radii and a function of support function. Under some appropriate assumptions, we prove the long-time existence and convergence of this flow. As an application, we give the existence of smooth solutions to the Orlicz–Christoffel–Minkowski problem.

Summary: Plants evolved sophisticated machineries to monitor levels of external nitrogen supply, respond to nitrogen demand from different tissues and integrate this information for coordinating its assimilation. Although roles of inorganic nitrogen in orchestrating developments have been studied in model plants and crops, systematic understanding of the origin and evolution of its assimilation and signaling machineries remains largely unknown.We expanded taxon samplings of algae and early‐diverging land plants, covering all main lineages of Archaeplastida, and reconstructed the evolutionary history of core components involved in inorganic nitrogen assimilation and signaling.Most components associated with inorganic nitrogen assimilation were derived from the ancestral Archaeplastida. Improvements of assimilation machineries by gene duplications and horizontal gene transfers were evident during plant terrestrialization. Clusterization of genes encoding nitrate assimilation proteins might be an adaptive strategy for algae to cope with changeable nitrate availability in different habitats. Green plants evolved complex nitrate signaling machinery that was stepwise improved by domains shuffling and regulation co‐option.Our study highlights innovations in inorganic nitrogen assimilation and signaling machineries, ranging from molecular modifications of proteins to genomic rearrangements, which shaped developmental and metabolic adaptations of plants to changeable nutrient availability in environments. [ABSTRACT FROM AUTHOR]

The BAP module, comprising BRASSINAZOLE RESISTANT 1 (BZR1), AUXIN RESPONSE FACTOR 6 (ARF6), and PHYTOCHROME‐INTERACTING FACTOR 4 (PIF4), functions as a molecular hub to orchestrate plant growth and development. In Arabidopsis thaliana, components of the BAP module physically interact to form a complex system that integrates light, brassinosteroid (BR), and auxin signals. Little is known about the origin and evolution of the BAP module. Here, we conducted comparative genomic and transcriptomic analyses to investigate the evolution and functional diversification of the BAP module. Our results suggest that the BAP module originated in land plants and that the ζ, ε, and γ whole‐genome duplication/triplication events contributed to the expansion of BAP module components in seed plants. Comparative transcriptomic analysis suggested that the prototype BAP module arose in Marchantia polymorpha, experienced stepwise evolution, and became established as a mature regulatory system in seed plants. We developed a formula to calculate the signal transduction productivity of the BAP module and demonstrate that more crosstalk among components enables higher signal transduction efficiency. Our results reveal the evolutionary history of the BAP module and provide insights into the evolution of plant signaling networks and the strategies employed by plants to integrate environmental and endogenous signals. [ABSTRACT FROM AUTHOR]

Children's Vitamin D (VitD) fortification and supplementation are diminishing due to less outdoor exercise and insufficient VitD intake (low exogenous intake and endogenous malabsorption induced by gastrointestinal disease). Consequently, children in many developed countries suffer from VitD deficiency, which may contribute to many paediatric disorders. Our review briefly introduced the metabolic process of VitD, summarized the role of VitD in paediatric diseases such as autism, obesity, rickets and asthma. We sought to identify the link between VitD deficiency and these diseases. [ABSTRACT FROM AUTHOR]

Ternary metal sulfides normally have narrow band gap energy levels, leading to fast recombination of photogenerated carriers. The construction of heterojunctions is generally believed to boost the photogenerated carrier efficiency via capturing and transferring electrons, and thus improving the photocatalytic activity. In this paper, different ratios of AgInS2–SnIn4S8 composites were synthesized by a microwave-assisted hydrothermal method, and the molar ratio of SnIn4S8:AgInS2 = 0.5:1 is determined as the optimal ratio based on the experimental results of visible photocatalytic degradation of methyl orange (MO). Furthermore, AgIn5S8/AgInS2–SnIn4S8 composites were successfully prepared by changing the ratio of In, S element, and AgNO3. The component, structural morphology, and surface physicochemical properties of the composites were characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, ultraviolet–visible diffuse reflectance absorption spectroscopy, and nitrogen adsorption–desorption tests. The results show that AgInS2 and AgIn5S8 are compounded with SnIn4S8 to form a heterogeneous structure. After the formation of heterogeneous structures, light absorption properties are changed and light absorption range is broadened due to stronger light absorption capacity in AgInS2 and AgIn5S8. As they have matched energy band structures, the electron transfer paths are increased and the e−–h+ lifetime is prolonged, which leads to enhanced photocatalytic performance of AgIn5S8/AgInS2–SnIn4S8 composites. Moreover, the formation of regular and homogeneous flower globose structure under the effect of microwave polarization also has an important contribution to the improvement of their photocatalytic performance. AgIn5S8/AgInS2–SnIn4S8 composites exhibit a certain degradation ability towards MO, and the degradation is almost complete within 180 min under visible light irradiation. Finally, through trapping experiments with the addition of different radical trapping agents and the ESR tests, photocatalytic active species are identified, and thus the possible photocatalytic reaction mechanism of AgIn5S8/AgInS2–SnIn4S8 composite is inferred. [ABSTRACT FROM AUTHOR]

We study a transport equation with nonlocal velocity and power law type damping. We show that a certain class of initial data smooth solution blows up in finite time. [ABSTRACT FROM AUTHOR]

Emerging rechargeable aluminium batteries (RABs) offer a sustainable option for next‐generation energy storage technologies with low cost and exemplary safety. However, the development of RABs is restricted by the limited availability of high‐performance cathode materials. Herein, we report two polyimide two‐dimensional covalent organic frameworks (2D‐COFs) cathodes with redox‐bipolar capability in RAB. The optimal 2D‐COF electrode achieves a high specific capacity of 132 mAh g−1. Notably, the electrode presents long‐term cycling stability (with a negligible ≈0.0007 % capacity decay per cycle), outperforming early reported organic RAB cathodes. 2D‐COFs integrate n‐type imide and p‐type triazine active centres into the periodic porous polymer skeleton. With multiple characterizations, we elucidate the unique Faradaic reaction of the 2D‐COF electrode, which involves AlCl2+ and AlCl4− dual‐ions as charge carriers. This work paves the avenue toward novel organic cathodes in RABs. [ABSTRACT FROM AUTHOR]

Neuartige Aluminium‐Akkumulatoren (AlAKs) stellen eine nachhaltige Option für Energiespeichertechnologien der nächsten Generation mit niedrigen Kosten und beispielhafter Sicherheit dar. Die Entwicklung von AlAKs wird jedoch durch die begrenzte Verfügbarkeit von Hochleistungs‐Kathodenmaterialien eingeschränkt. In diesem Artikel beschreiben wir zwei Polyimid‐ basierte zweidimensionale Covalent‐Organic‐Framework‐ (2D COF) Elektrodenmaterialien mit redox‐bipolarer Fähigkeit in AlAKs. Die optimierte 2D‐COF‐Elektrode erreicht eine hohe spezifische Kapazität von 132 mAh g−1. Die Elektrode weist eine langfristige Zyklenstabilität auf (mit einem vernachlässigbaren Kapazitätsabfall von ≈0.0007 % pro Zyklus) und übertrifft damit frühere Ergebnisse organischer AlAK‐Kathoden. Unsere 2D‐COFs beinhalten n‐Type‐Imide und p‐Type‐Triazine als aktive Zentren im periodisch‐porösen Polymerskelett. Anhand umfänglicher Charakterisierungen erklären wir die ungewöhnliche Faradische Reaktion der 2D‐COF‐Elektrode, bei der AlCl2+‐ und AlCl4− Dualionen als Ladungsträger beteiligt sind. Diese Arbeit ebnet den Weg zu neuartigen organischen Kathodenmaterialien in AlAKs. [ABSTRACT FROM AUTHOR]

DNA methylation plays important roles through the methyl-CpG-binding domain (MBD) to realize epigenetic modifications. Thirteen AtMBD proteins have been identified from the Arabidopsis thaliana genome, but the functions of some members are unclear. AtMBD3 was found to be highly expressed in pollen and seeds and it preferably binds methylated CG, CHG, and unmethylated DNA sequences. Then, two mutant alleles at the AtMBD3 locus were obtained in order to further explore its function using CRISPR/Cas9. When compared with 92.17% mature pollen production in the wild type, significantly lower percentages of 84.31% and 78.91% were observed in the mbd3-1 and mbd3-2 mutants, respectively. About 16–21% of pollen from the mbd3 mutants suffered a collapse in reproductive transmission, whereas the other pollen was found to be normal. After pollination, about 16% and 24% of mbd3-1 and mbd3-2 mutant seeds underwent early or late abortion, respectively. Among all the late abortion seeds in mbd3-2 plants, 25% of the abnormal seeds were at the globular stage, 31.25% were at the transition stage, and 43.75% were at the heart stage. A transcriptome analysis of the seeds found 950 upregulated genes and 1128 downregulated genes between wild type and mbd3-2 mutants. Some transcriptional factors involved in embryo development were selected to be expressed, and we found significant differences between wild type and mbd3 mutants, such as WOXs, CUC1, AIB4, and RGL3. Furthermore, we found a gene that is specifically expressed in pollen, named PBL6. PBL6 was found to directly interact with AtMBD3. Our results provide insights into the function of AtMBD3 in plants, especially in sperm fertility. [ABSTRACT FROM AUTHOR]