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Although significant amounts of methane are present in anthracite coal seams, coalbed methane resources cannot be extracted effectively and quickly. This study mainly focused on investigating the pore system and methane adsorption capacity to clarify the storage of coalbed methane. Anthracite coal samples from the Anzenan coalbed methane block in China were collected, and pore characterization methods (low-pressure N2 adsorption, mercury injection experiments, and scanning electron microscopy (SEM) observations) and methane isothermal adsorption experiments were conducted. The results showed that few mesopores and nanoscale macropores were present in the anthracite coal samples. The volume of the 2–300 nm pores in these coal samples obtained from the N2 adsorption experiment was lower than 0.01 cm3/g. SEM observations also revealed that only a small number of mesopores and nanoscale macropores could be seen, and most of these pores were isolated. In terms of the methane isothermal adsorption data, it was found these anthracite coals have a large methane adsorption capacity, and the Langmuir volume ranges from 19.5 to 28.4 cm3/g, with an average of 22.2 cm3/g. With increasing ash yield, the Langmuir volume decreased linearly, indicating that methane molecules were mainly adsorbed in the organic matter of coal. As methane is mainly adsorbed in the micropores of coal organic matter and there are few mesopores and nanoscale macropores in the organic pores in coal, there are not enough tunnels to transport the adsorbed methane molecules to the outside. Thus, it is difficult to extract coalbed methane from anthracite. This study reveals the impact of pore system limitations on the storage and extraction of coalbed methane in anthracite coal. The findings can be applied to the extraction of coalbed methane from anthracite coal seams worldwide.

The main purpose of this study was to improve the function and quality of frozen purple sweet potato cubes. In this study, osmotic dehydration (OD), natural drying, hot air drying and freeze drying (FD) were used as pretreatment methods to evaluate the changes in anthocyanin composition of purple sweet potato after freezing and thawing, and to identify the most effective pretreatment methods to reduce the loss of anthocyanin in the freeze-thawing process. The results showed that after freezing and thawing, OD-treated purple sweet potato exhibited a significant decrease in total colordifference compared with the other pretreatment groups (P < 0.05), and the colour was closest to that of the fresh samples. Compared with other treatment groups, OD and FD pretreatment could significantly inhibit the polyphenol oxidase (PPO) and peroxidase (POD) activities of purple sweet potato after dehydration (P < 0.05), while the OD-treated group had the lowest PPO and POD activities. The 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging capacity and total antioxidant capacity were maintained at a higher level in the OD- and FD-treated groups compared to the other pretreatment groups. Twenty-seven Anthocyanins in purple sweet potato were lost after freezing and thawing. Compared with other pretreatments, OD pretreatment minimised the loss of anthocyanins after dehydration and freeze-thawing of purple potato cubes. Therefore, OD is the most effective pretreatment method for anthocyanin protection infrozen purple sweet potato, which is suitable for freezing storage of purple sweet potato to be used for anthocyanin extraction.

The proliferation and differentiation of myoblasts are considered the key biological processes in muscle development and muscle-related diseases, in which the miRNAs involved remain incompletely understood. Previous research reported that miR-424(322)-5p is highly expressed in mouse skeletal muscle. Therefore, C2C12 cells are used as a model to clarify the effect of miR-424(322)-5p on the proliferation and differentiation of myoblasts. The data show that miR-424(322)-5p exhibits a decreasing trend upon myogenic differentiation. Overexpression of miR-424(322)-5p inhibits the proliferation of myoblasts, manifested by downregulation of proliferation marker genes ( CCNB1, CCND2, and CDK4), decreased percentage of EdU + cells, and reduced cell viability. In contrast, these phenotypes are promoted in myoblasts treated with an inhibitor of miR-424(322)-5p. Interestingly, its gain of function inhibits the expression of myogenic regulators, including MyoD, MyoG, MyHC, and Myf5. Additionally, immunofluorescence staining of MyHC and MyoD shows that overexpression of miR-424(322)-5p reduces the number of myotubes and decreases the myotube fusion index. Consistently, inhibition of its function mediated by an inhibitor promotes the expressions of myogenic markers and myotube fusion. Mechanistically, gene prediction and dual-luciferase reporter experiments confirm that enhancer of zeste homolog 1 ( Ezh1) is one of the targets of miR-424(322)-5p. Furthermore, knockdown of Ezh1 inhibits the proliferation and differentiation of myoblasts. Compared with NC and inhibitor treatment, inhibitor+si- EZH1 treatment rescues the phenotypes of proliferation and differentiation mediated by the miR-424(322)-5p inhibitor. Taken together, these data indicate that miR-424(322)-5p targets Ezh1 to negatively regulate the proliferation and differentiation of myoblasts.

Large residual stress induced by significant difference in the coefficient of thermal expansion compromises the mechanical performance of a brazed joint between the WC–Co cemented carbide (YG20) and 3Cr13 stainless steel in a cutting tool of shield machine. In this study, a melamine formaldehyde foam precursor was utilized to produce a 3D hollow carbon foam (HCF) used as interlayer through a high‐temperature carbonization process to aid in the brazing process of YG20 and 3Cr13. First, the morphology and microstructure of the HCF interlayer were revealed as a defect‐rich carbon shell with a hollow structure. Afterward, the effects of introducing the as‐prepared HCF interlayer on the joint microstructure and shear performance were investigated. Results indicate that the HCF interlayer contributed to phase homogenization and, moreover, the residual stress relieving through in situ forming a core (metallic matrix)–sheath (ceramic shell) structure. This method outperformed the direct brazing approach without using an interlayer, with a 41% increase in the joint shear strength due to the synergistic strengthening mechanism of the HCF through residual stress reliving and joint seam toughening. Based on the results, in spite of the residual stress, the fast load transfer and the compensation from the matrix core to the ceramic sheath are responsible for the improved mechanical performance of the joint. [ABSTRACT FROM AUTHOR]

Objective: The main pathological change of myocarditis is an inflammatory injury of cardiomyocytes. Long noncoding RNAs (lncRNAs) are closely related to inflammation, and our previous study showed that differential expression of lncRNAs is associated with myocarditis. This study aimed to investigate the impact of lncRNAs on the onset of myocarditis. Methods: RNA expression was measured by quantitative reverse-transcription polymerase chain reaction (RT-qPCR). Lipopolysaccharide (LPS) was used to induce inflammation in human cardiomyocytes (HCMs). The expression of inflammatory cytokines and myocardial injury markers was detected by enzyme-linked immunosorbent assay (ELISA) and RT-qPCR. Cell viability and apoptosis were measured by the cell counting kit-8 assay and flow cytometry. The binding force between lncRNA NONHSAT122636.2 and microRNA miRNA-2110 was detected using the dual-luciferase assay. Results: NONHSAT122636.2 was dynamically expressed in patients with myocarditis and negatively correlated with inflammation severity. The overexpression of NONHSAT122636.2 improved inflammatory injury in LPS-stimulated HCMs. The study observed that there was a weak binding force between NONHSAT122636.2 and miR-2110. Conclusion: NONHSAT122636.2 attenuates myocardial inflammation and apoptosis in myocarditis. Additionally, its expression decreases in the peripheral blood of children suffering from myocarditis and in patients who are diagnosed for the first time showing higher diagnostic sensitivity and specificity. This decrease is negatively correlated with the degree of inflammation. Overall, the study suggests that NONHSAT122636.2 can be exploited as a potential diagnostic biomarker for pediatric myocarditis. [ABSTRACT FROM AUTHOR]

Aims/Background Gestational diabetes mellitus is a common pregnancy complication that affects approximately 14% of pregnancies worldwide and can lead to adverse maternal and neonatal outcomes. This study aimed to investigate the trajectories of gestational weight gain among gestational diabetes mellitus patients and to inform the development of effective weight management strategies. Methods Demographic and antenatal examination data from 1421 pregnant women diagnosed with gestational diabetes mellitus were retrospectively analysed. Quantitative data comparisons were performed using Chi-square tests, Fisher's exact test, t-tests, and one-way analysis of variance. Group-based trajectory modelling was employed to identify the trajectories of gestational weight gain among patients with gestational diabetes mellitus. Results This study revealed that pre-pregnancy body mass index and types of gestational diabetes mellitus significantly influence gestational weight gain (p < 0.05). Group-based trajectory modelling identified three distinct gestational weight gain trajectories. Patients with gestational diabetes mellitus demonstrated a continuous weight gain throughout pregnancy, while women who were overweight or obese before pregnancy were more likely to follow a low-speed growth trajectory. Women in the rapid growth trajectory group were more inclined to deliver by caesarean section and were more likely to give birth to macrosomic infants. Conclusion Our research underscores the importance of identifying and distinguishing between different gestational weight gain trajectories in pregnant women, thereby identifying high-risk groups, which is crucial for improving the health conditions of both mothers and newborns. [ABSTRACT FROM AUTHOR]

The corrosion performances and tribological behaviors of β-type Ti–V–Al based biomedical shape memory alloys were systematically investigated through electrochemical experiments and reciprocating friction and wear tests. The results revealed significant distinctions in corrosion performances between the Ti–V–Al–Zr and Ti–V–Al–Sn shape memory alloys, which can be attributed to the difference in the types of oxides formed during the corrosion process. In comparison, Ti–V–Al based shape memory alloys exhibited superior corrosion properties by adding an Sn alloying element. In addition, adding the moderate Sn alloying element could significantly improve the wear resistance compared with Ti–V–Al–Zr shape memory alloys. In summary, the present study provided a theoretical basis for the selection of Ti–V–Al based shape memory alloys applied for various biomedical fields. [ABSTRACT FROM AUTHOR]

At present, the world is undergoing profound changes unseen in a century, and the international political and economic governance system is undergoing profound changes. Protectionism and antiglobalization are on the rise, and the normalization of COVID-19 prevention and control has intensified international investment and economic and trade frictions. The domestic and foreign environment faced by the overseas investment and merger of Chinese power enterprises is increasingly complex, and the potential risks and uncertainties are increasing. Combing the energy industry key risk points of transnational mergers and acquisitions, this paper analyse the energy industry transnational M&A project political risk and legal risk evaluation method, and put forward the company transnational M&A project political risk and legal risk prevention strategy.

Despite extensive research highlighting the pivotal role of MYB transcription factors in regulating anthocyanin biosynthesis, the interactive regulatory network involving these MYB factors in pear fruits remains inadequately characterized. In this study, the anthocyanin-regulatory gene PbrMYB114 was successfully cloned from 'Yuluxiang' pear (Pyrus bretschneideri) fruits, and its influence on anthocyanin accumulation was confirmed through transient expression assays. Specifically, the co-transformation of PbrMYB114 with its partner PbrbHLH3 in pears served to validate the functional role of PbrMYB114. Subsequently, PbrMYB114 was employed as bait in a yeast two-hybrid screening assay, using a 'Yuluxiang' pear protein library, which led to the identification of 25 interacting proteins. Further validation of the interactions between PbrMYB114 and PbrMT2/PbrMT3 was conducted. Investigations into the role of PbrMT2 and PbrMT3 in 'Duli' seedlings (Pyrus betulaefolia) revealed their potential to enhance anthocyanin accumulation. The outcomes of these studies provide novel insights into the protein network that regulates pear anthocyanin biosynthesis, particularly the functional interactions among PbrMYB114 and associated proteins. [ABSTRACT FROM AUTHOR]

The growth and development of apricot flower organs are severely impacted by spring frosts. To better understand this process, apricot flowers were exposed to temperatures ranging from 0 °C to −8 °C, including a control at 18 °C, in artificial incubators to mimic diverse low-temperature environments. We aimed to examine their physiological reactions to cold stress, with an emphasis on changes in phenotype, membrane stability, osmotic substance levels, and antioxidant enzyme performance. Results reveal that cold stress induces significant browning and cellular damage, with a sharp increase in browning rate and membrane permeability below −5 °C. Soluble sugars and proteins initially rise as osmoprotectants, but their content decreases at lower temperatures. Proline content consistently increases, suggesting a protective role. Antioxidant enzyme activities, including catalase (CAT), peroxidase (POD), superoxide dismutase (SOD), and ascorbate peroxidase (APX), exhibit a complex pattern, with initial increases followed by declines at more severe cold conditions. Correlation and principal component analyses highlight the interplay between these responses, indicating a multifaceted adaptation strategy. The findings contribute to the understanding of apricot cold tolerance and inform breeding efforts for improved crop resilience. [ABSTRACT FROM AUTHOR]