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This paper addresses the fault-tolerant performance of real-time dual-computer embedded systems. The article first emphasizes the importance of real-time and reliability in various fields and points out that improving fault-tolerant performance is a crucial topic. Based on the Markov chain algorithm, the study optimizes the fault-tolerant integration method for real-time dual-computer embedded systems. By constructing a model of Markov algorithm and using the deadline of the task as a benchmark, the passage and transfer probabilities of faults are calculated. The article also provides algorithmic proofs of fault-tolerant control of Markovian jump systems and calculates their stability levels. The results show that the fault passage rate of the system increases as the number of complex tasks increases, e.g., when the number of complex tasks is 4, the passage rate can reach 90%. In addition, in the scheduling test, it was found that the schedulability of the system increases with the increase in the number of processors. When the number of processors reaches 5, the system's schedulability is 43%. In conclusion, the system fault tolerance optimization method based on Markov algorithm proposed in the article can effectively improve the reliability and fault tolerance of the system.

To improve the complexity and low catalytic performance and reduce the high cost of the traditional electrode preparation process for the sodium borohydride electro-oxidation reaction (BOR), in this work, a self-supported and efficient electrode material grown on nickel foam (CoNi/Co3O4/NF) was successfully designed using a simple hydrothermal synthesis method accompanied by the electrodeposition process. Benefiting from the three-dimensional nanoarray structure of CoNi/Co3O4/NF and the uniform distribution of Co and Ni modulating active sites by electrodeposition, the catalytic activity towards NaBH4 exhibits high efficiency. CoNi/Co3O4 exhibits excellent catalytic performance (up to 2157 mA cm−2 in 2 mol L−1 NaOH and 0.3 mol L−1 NaBH4), a high electrochemically active surface area (62.5 cm−2), and a low activation energy (15.56 kJ mol−1). The CoNi/Co3O4/NF electrode was further investigated on a direct sodium borohydride–hydrogen peroxide fuel cell (DBHPFC), which exhibited a maximum power density of 108.5 mW cm−2 and excellent stability. The excellent performance is mainly due to its unique nanoarray structure and electrodeposition distribution of Co and Ni active sites, which increases the electrochemical surface area and enhances the contact between the electrode and the electrolyte. [ABSTRACT FROM AUTHOR]

Ampullofolliculina Hadži, 1951 is a monotypic genus, the only species being A. lageniformis which was first discovered in estuarine habitats in the U.S. and has never been redescribed. In the present study, we investigated the taxonomy and phylogeny of A. lageniformis Hadži, 1951 based on analyses of a population collected from a brackish wetland in Ningbo, China. The main characteristics of this species are as follows: trophont about 450–700 μm long in vivo with two short, rounded peristomial lobes of equal size; lorica flask‐shaped, transparent and smooth with a short, wide neck at the base of which two transparent valves are asymmetrically inserted; cortex with brownish to reddish cortical granules and greenish pigment granules; about 80 somatic kineties evenly arranged; moniliform macronucleus with 4–8 ellipsoidal nodules; swarmer dark green, vermiform in shape, about 200–350 μm long in vivo, with about 60 adoral membranelles and 85 somatic kineties, no mouth nor paroral membrane. Phylogenetic analyses inferred from SSU rDNA sequences show that A. lageniformis is closely related to Folliculina and Eufolliculina which nest within a large clade that comprises five families, i.e. Stentoridae, Blepharismidae, Fabreidae, Maristentoridae, and Folliculinidae. [ABSTRACT FROM AUTHOR]

Two new polyoxometalate-based coordination polymers have been synthesized at different pHs under identical hydrothermal conditions, (Hbib)[Cu2(bib)2(PMo12O40)] (1) and (Hbib)2[Cu(bib) (PMo12O40)]·2H2O (2) (bib = 4-bis(imidazol-1-yl) benzene). Their structures were determined by single crystal X-ray diffraction analyses and characterized by routine methods. When the pH was adjusted to 2.0 − 2.5, 1 was obtained, which exhibits a 1-D rail-like chain. Compound 2 was obtained at pH of 2.5 − 3.2 and exhibits a 2-D layer with (44) sql net. The pH of the reaction plays a key role in the assembly of the polyoxometalate-based coordination polymer. The electrochemical experiments indicate that 2-based carbon paste electrode possesses high catalytic efficiency and high stability towards reduction of iodate and oxidation of ascorbic acid. [ABSTRACT FROM AUTHOR]

The temporal dynamics of ciliate community structure in a southern Chinese shrimp aquaculture facility were investigated during the period June–September 2012. A total of 53 species belonging to 37 genera and 17 orders were recorded based on analyses of eight samples. Ciliate abundance peaked between 16 August and 14 September 2012, while the maximum number of species occurred on 26 June 2012. Clear temporal patterns were observed in the ciliate community structure. The patterns of succession of the 10 most abundant species were consistent with the results of a Canonical Analysis of Principal coordinates (CAP) analysis. Correlation analyses showed that these patterns of succession were related to temporal changes in environmental variables. In summary, the results demonstrate that the ciliate community responds predictably to environmental variations and recovers from shrimp cultivation. [ABSTRACT FROM AUTHOR]