[go: up one dir, main page]

 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (296,570)

Search Parameters:
Keywords = mechanical

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
13 pages, 2160 KiB  
Article
Boosting Expression of a Specifically Targeted Antimicrobial Peptide K in Pichia pastoris by Employing a 2A Self-Cleaving Peptide-Based Expression System
by Yunhui Zhu, Yuwen Li, Yuxin Fang, Mingyang Hu, Lu Zhao, Mingrui Sui and Na Dong
Antibiotics 2024, 13(10), 986; https://doi.org/10.3390/antibiotics13100986 (registering DOI) - 18 Oct 2024
Abstract
Background/Objectives: The current epidemic of drug-resistance bacterial strains is one of the most urgent threats to human health. Antimicrobial peptides (AMPs) are known for their good activity against multidrug resistance bacteria. Specifically targeted AMPs (STAMPs) are a fraction of AMPs that target specific [...] Read more.
Background/Objectives: The current epidemic of drug-resistance bacterial strains is one of the most urgent threats to human health. Antimicrobial peptides (AMPs) are known for their good activity against multidrug resistance bacteria. Specifically targeted AMPs (STAMPs) are a fraction of AMPs that target specific bacteria and maintain the balance of the healthy microbiota of a host. We reported a STAMP Peptide K (former name: peptide 13) for E. coli. The aim of this study was to effectively produce peptide K using methylotrophic yeast Pichia pastoris. Methods: Three inserts (sequence of peptide K (K), two copies of peptide K fused with 2A sequence (KTK), and two copies of peptide K fused with 2A and an extra α mating factor (KTAK)) were designed to investigate the effect of the number of repeats and the trafficking of peptide on the yield. Results: The yield from KTK was the highest—more than two-fold higher compared with K—implying the role of the 2A sequence in heterologous peptide expression apart from the co-translation. Then, the fermentation condition for KTK was optimized. The optimized yield of KTK was 6.67 mg/mL, suggesting the efficiency of the expression system. Selectivity, antibacterial activity, biocompatibility, and the stability of the fermentation product were equivalent to the chemically synthesized peptide. The actional mechanism of the fermentation product included membrane permeabilization and ROS induction. Conclusions: Together, our work provided a new perspective to augment the yield of the antimicrobial peptide in the microbial system, building a technological foundation for their large-scale production and expanding the market application of AMPs. Full article
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Structure of pPIC9K plasmid and schematic diagram showing the alignment of K, KTK, and KTAK. (<b>b</b>) Agar gel electrophoresis for the recombinant plasmid. M: marker; E: pPIC9K; K: peptide K; T: KTK; A: KTAK. (<b>c</b>) Screening of positive transformants on MD plate. (<b>d</b>) PCR agar gel electrophoresis for monoclonal recombinant GS115 with universal primer <span class="html-italic">AOX</span>.</p>
Full article ">Figure 2
<p>(<b>a</b>) Time growth of GS115. The culture parameters for the growth curve were a single colony of GS115 with empty vector in BMGY, growing at 30 °C in a shaking incubator 250 rpm. (<b>b</b>) Wet weight of recombinant GS115. (<b>c</b>) Tricine-SDS-PAGE for fermentation products from recombinant GS115. MW: molecular weight; E: supernatant from GS115 containing empty vector; K: supernatant from GS115 containing K; T: supernatant from GS115 containing KTAK; A: supernatant from GS115 containing KTAK. (<b>d</b>) The antibacterial activity of fermentation supernatant. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; **** <span class="html-italic">p</span> &lt; 0.0001.</p>
Full article ">Figure 3
<p>Expression of peptide K at different fermentation time (<b>a</b>) with different methanol concentration (<b>b</b>) and with different pH value (<b>c</b>). M: marker.</p>
Full article ">Figure 4
<p>(<b>a</b>) Purification of recombinant peptide K. M: marker; K<sub>S</sub>: fermentation supernatant; K<sub>P</sub>: purified recombinant peptide K. (<b>b</b>) Hemolysis of purified peptide K from KTK. (<b>c</b>) Membrane permeability of recombinant peptide K using NPN method. (<b>d</b>) ROS production induced by recombinant peptide K using DCFH method. ME: melittin.</p>
Full article ">
18 pages, 6828 KiB  
Article
Characterization of Atlantic Forest Tucum (Bactris setosa Mart.) Leaf Fibers: Aspects of Innovation, Waste Valorization and Sustainability
by Taynara Thaís Flohr, Eduardo Guilherme Cividini Neiva, Marina Proença Dantas, Rúbia Carvalho Gomes Corrêa, Natália Ueda Yamaguchi, Rosane Marina Peralta, Afonso Henrique da Silva Júnior, Joziel Aparecido da Cruz, Catia Rosana Lange de Aguiar and Carlos Rafael Silva de Oliveira
Plants 2024, 13(20), 2916; https://doi.org/10.3390/plants13202916 (registering DOI) - 18 Oct 2024
Abstract
This study investigates the fibers of tucum (Bactris setosa Mart.), a palm species native to the Atlantic Forest. The fibers manually extracted from tucum leaves were characterized to determine important properties that help with the recognition of the material. The fibers were [...] Read more.
This study investigates the fibers of tucum (Bactris setosa Mart.), a palm species native to the Atlantic Forest. The fibers manually extracted from tucum leaves were characterized to determine important properties that help with the recognition of the material. The fibers were also subjected to pre-bleaching to evaluate their dyeing potential. The extraction and characterization of these fibers revealed excellent properties, making this material suitable not only for manufacturing high-quality textile products but also for various technical and engineering applications. The characterization techniques included SEM (Scanning Electron Microscopy), FTIR (Fourier Transform Infrared Spectroscopy), TGA (Thermogravimetric Analysis), and tensile strength tests. These analyses showed that tucum fibers possess desirable properties, such as high tensile strength, with values comparable to linen but with a much finer diameter. The fibers also demonstrated good affinity for dyes, comparable to cotton fibers. An SEM analysis revealed a rough surface, with superficial phytoliths contributing to their excellent mechanical strength. FTIR presented a spectrum compatible with cellulose, confirming its main composition and highly hydrophilic nature. The dyeing tests indicated that tucum fibers can be successfully dyed with industrial direct dyes, showing good color yield and uniformity. This study highlights the potential of tucum fibers as a renewable, biodegradable, and sustainable alternative for the transformation industry, promoting waste valorization. Full article
Show Figures

Figure 1

Figure 1
<p>Tucum palm (<span class="html-italic">Bactris setosa</span> Mart.): (<b>a</b>) records of occurrences of the species <span class="html-italic">Bactris setosa</span> Mart. in Brazil (reproduced with permission from [<a href="#B25-plants-13-02916" class="html-bibr">25</a>]); (<b>b</b>) map of the geographic distribution of the species <span class="html-italic">Bactris setosa</span> Mart. in the Brazilian state of Santa Catarina (Reproduced with permission from [<a href="#B26-plants-13-02916" class="html-bibr">26</a>]); (<b>c</b>) clump from which samples were taken; (<b>d</b>) green fruit of the tucum palm; (<b>e</b>) detail of the thorns on the rachis of the tucum leaf; (<b>f</b>) ripe fruit of the tucum palm, from left to right: first, the fruit with its outer skin; next, the same fruit without the skin, exposing the pulp; and finally, the whole and broken almond, from which tucum oil is extracted.</p>
Full article ">Figure 2
<p>SEM analysis of raw tucum fibers: (<b>a</b>) panoramic view of the cross-section of a tucum fiber from its end, magnification of 3600×; (<b>b</b>) longitudinal view of tucum fibers, magnification of 7000×; (<b>c</b>) EDS analysis of tucum fiber, the black curve represents the EDS spectrum of the surface in a region without phytoliths, while the red curve represents the spectrum from the region containing the phytolith.</p>
Full article ">Figure 3
<p>SEM analysis of manually extracted raw tucum fibers and pre-bleached fiber: (<b>a</b>) photographic image of a bundle of raw fibers (before pre-bleaching); (<b>b</b>,<b>c</b>) longitudinal view of the manually extracted raw fiber, with magnifications of 300× and 5800×, respectively. (<b>d</b>) photographic image of a bundle of pre-bleached fibers; (<b>e</b>,<b>f</b>) longitudinal view of the pre-bleached fiber with H<sub>2</sub>O<sub>2</sub>, with magnifications of 295× and 5300×, respectively.</p>
Full article ">Figure 4
<p>Determination of the average fiber length: (<b>a</b>) shape of the tucum palm leaf × length of the leaflets; (<b>b</b>) variation in leaflet sizes depending on the region of the leaf; (<b>c</b>) histogram of fiber length distribution of the analyzed sample.</p>
Full article ">Figure 5
<p>Characterization analysis of manually-extracted tucum fibers: (<b>a</b>) FTIR analysis of the raw tucum fiber; (<b>b</b>) TGA-DTG analysis of the raw tucum fiber; (<b>c</b>) Zeta Potential analysis of the raw tucum fiber; (<b>d</b>) stress–strain analysis of the raw tucum fiber.</p>
Full article ">Figure 6
<p>Comparison of dyed samples and their respective residual dye baths: (<b>a</b>) cotton fabric; (<b>b</b>) viscose fabric; (<b>c</b>) tucum fiber.</p>
Full article ">Figure 7
<p>Steps of the manual process of fiber extraction from the leaves of the genus <span class="html-italic">Bactris setosa</span> Mart.: (<b>a</b>) tucum leaf; (<b>b</b>) manual process of tucum fiber extraction; (<b>c</b>) the leaflets were removed from the rachis, then a fold was made near the tip of the leaflet, creating a crease; (<b>d</b>,<b>e</b>) after folding the crease, the epidermis of the leaflet was pulled, promoting the release of the fibers along the entire leaflet, and this process could be repeated up to five times for complete extraction.</p>
Full article ">Figure 8
<p>Treatment parameters of the raw fibers: (<b>a</b>) placement of the fibers in a small tulle fabric pouch; (<b>b</b>) temperature curve of the pre-bleaching process; (<b>c</b>) molecule of the dye used in the dyeing of fiber and fabric samples; (<b>d</b>) temperature curve of the dyeing process.</p>
Full article ">
14 pages, 5184 KiB  
Article
Sustainable Composites from Waste Polypropylene Added with Thermoset Composite Waste or Recovered Carbon Fibres
by Ehsan Zolfaghari, Giulia Infurna, Sabina Alessi, Clelia Dispenza and Nadka Tz. Dintcheva
Polymers 2024, 16(20), 2922; https://doi.org/10.3390/polym16202922 (registering DOI) - 18 Oct 2024
Abstract
In order to limit the ever-increasing consumption of new resources for material formulations, regulations and legislation require us to move from a linear to a circular economy and to find efficient ways to recycle, reuse and recover materials. Taking into account the principles [...] Read more.
In order to limit the ever-increasing consumption of new resources for material formulations, regulations and legislation require us to move from a linear to a circular economy and to find efficient ways to recycle, reuse and recover materials. Taking into account the principles of material circularity and waste reuse, this research study aims to produce thermoplastic composites using two types of industrial waste from neighbouring companies, namely waste polypropylene (wPP) from household production and carbon-fibre-reinforced epoxy composite scrap from a pultrusion company. The industrial scrap of the carbon-fibre-reinforced epoxy composites was either machined/ground to powder (pCFRC) and used directly as a reinforcement agent or subjected to a chemical digestion process to recover the carbon fibres (rCFs). Both pCFRC and rCF, at different weight ratios, were melt-blended with wPP. Prior to melt blending, both pCFRC and rCF were analysed for morphology by scanning electron microscopy (SEM). The pCFRC powder contains epoxy resin fragments with spherical to ellipsoidal shape and carbon fibre fragments. The rCFs are clean from the matrix, but they are slightly thicker and corrugated after the matrix digestion. Further, the morphologies of wPP/pCFRC and wPP/rCF were also investigated by SEM, while the thermal behaviour, i.e., transitions and changes in crystallinity, and thermal resistance were evaluated by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), respectively. The strength of the interaction between the filler (i.e., pCFRC or rCF) and the wPP matrix and the processability of these composites were assessed by rheological studies. Finally, the mechanical properties of the systems were characterised by tensile tests, and as found, both pCFRC and rCF exert reinforcement effects, although better results were obtained using rCF. The wPP/pCFRC results are more heterogeneous than those of the wPP/rCF due to the presence of epoxy and carbon fibre fragments, and this heterogeneity could be considered responsible for the mechanical behaviour. Further, the presence of both pCFRC and rCF leads to a restriction of polymer chain mobility, which leads to an overall reduction in ductility. All the results obtained suggest that both pCFRC and rCF are good candidates as reinforcing fillers for wPP and that these complex systems could potentially be processed by injection or compression moulding. Full article
(This article belongs to the Special Issue Progress in Recycling of (Bio)Polymers and Composites, 2nd Edition)
Show Figures

Figure 1

Figure 1
<p>SEM images of the reinforcing additives at different magnifications: (<b>a</b>) virgin carbon fibre (vCF), (<b>b</b>) recovered fibres after matrix digestion (rCFs) and (<b>c</b>) powder (pCFRC).</p>
Full article ">Figure 2
<p>DSC traces of first and second heating (endotherm-down) and first cooling (exotherm-up) cycles for different composite formulations: (<b>a</b>) wPP alone, (<b>b</b>–<b>d</b>) wPP/pCFRC at varying concentrations of pCFRC and (<b>e</b>,<b>f</b>) wPP/rCF composites at two different rCF ratios.</p>
Full article ">Figure 3
<p>(<b>a</b>,<b>b</b>) TGA traces and (<b>c</b>,<b>d</b>) heat flow traces of wPP/pCFRC and wPP/rCF composites (endotherm-down); for comparison, the traces of wPP are also shown.</p>
Full article ">Figure 4
<p>Rheological data for composite materials: (<b>a</b>) complex viscosity vs. angular frequency for all samples, (<b>b</b>) G′ and G″ moduli vs. angular frequency for wPP/pCFRC composites at different concentrations of pCFRC and (<b>c</b>) G′ and G″ moduli vs. angular frequency for wPP/rCF composites at various rCF ratios.</p>
Full article ">Figure 5
<p>SEM images at identical magnifications: (<b>a</b>) wPP alone, (<b>b</b>–<b>d</b>) wPP/pCFRC at different concentrations of pCFRC and (<b>e</b>,<b>f</b>) wPP/rCF composites at various rCF ratios.</p>
Full article ">Figure 6
<p>ATR-FTIR spectra of wPP and composite materials: (<b>a</b>) wPP/pCFRC and (<b>b</b>) wPP/rCF composites.</p>
Full article ">Figure 7
<p>Mechanical properties of composite materials: (<b>a</b>) Young’s modulus, E; (<b>b</b>) tensile strength, TS; and (<b>c</b>) elongation at break, EB, of wPP and all wPP composites at different reinforcement concentrations.</p>
Full article ">Scheme 1
<p>Overall degradation and stabilisation pathways of PP under thermo-mechanical stress, which illustrates the formation of free radicals in the absence of antioxidants, leading to a degradation of products (readapted from [<a href="#B37-polymers-16-02922" class="html-bibr">37</a>]).</p>
Full article ">
19 pages, 3079 KiB  
Review
Opportunities and Challenges of Multi-Ion, Dual-Ion and Single-Ion Intercalation in Phosphate-Based Polyanionic Cathodes for Zinc-Ion Batteries
by Lei Cao, Tao Du, Hao Wang, Zhen-Yu Cheng, Yi-Song Wang and Li-Feng Zhou
Molecules 2024, 29(20), 4929; https://doi.org/10.3390/molecules29204929 (registering DOI) - 18 Oct 2024
Abstract
Abstract: With the continuous development of science and technology, battery storage systems for clean energy have become crucial for global economic transformation. Among various rechargeable batteries, lithium-ion batteries are widely used, but face issues like limited resources, high costs, and safety concerns. In [...] Read more.
Abstract: With the continuous development of science and technology, battery storage systems for clean energy have become crucial for global economic transformation. Among various rechargeable batteries, lithium-ion batteries are widely used, but face issues like limited resources, high costs, and safety concerns. In contrast, zinc-ion batteries, as a complement to lithium-ion batteries, are drawing increasing attention. In the exploration of zinc-ion batteries, especially of phosphate-based cathodes, the battery action mechanism has a profound impact on the battery performance. In this paper, we first review the interaction mechanism of multi-ion, dual-ion, and single-ion water zinc batteries. Then, the impact of the above mechanisms on battery performance was discussed. Finally, the application prospects of the effective use of multi-ion, dual-ion, and single-ion intercalation technology in zinc-ion batteries is reviewed, which has significance for guiding the development of rechargeable water zinc-ion batteries in the future. Full article
(This article belongs to the Special Issue Novel Electrode Materials for Rechargeable Batteries, 2nd Edition)
Show Figures

Figure 1

Figure 1
<p>Schematic representation of multiple ion insertion mechanisms in rechargeable zinc phosphate-based batteries.</p>
Full article ">Figure 2
<p>Schematic diagram of different batteries and their advantages and disadvantages. (<b>a</b>) Schematic diagram of Zn-LiFePO<sub>4</sub> aqueous rechargeable battery; (<b>b</b>) schematic diagram of Zn-Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>2</sub>F<sub>3</sub> aqueous rechargeable battery; and (<b>c</b>) schematic diagram of Zn-VOPO<sub>4</sub> rechargeable battery in the electrolyte 21 M LiTFSI/1 M Zn (Tr)<sub>2</sub> solution.</p>
Full article ">Figure 3
<p>(<b>a</b>) Charge-discharge curves of Zn-LiFePO<sub>4</sub> [<a href="#B3-molecules-29-04929" class="html-bibr">3</a>]; Copyright© 2013 Copyright Clearance Center, Inc. All rights reserved, United Kingdom of Great Britain and Northern Ireland (<b>b</b>) Initial charge–discharge curves of Li<sub>3</sub>V<sub>2−x</sub>Mn<sub>x</sub>(PO<sub>4</sub>)<sub>3</sub> (x = 0.00, 0.02, 0.04, 0.06, 0.1) [<a href="#B41-molecules-29-04929" class="html-bibr">41</a>]; Copyright© 2023 Advanced Energy Materials, published by Wiley-VCH GmbH, American (<b>c</b>) Charge–discharge curves of Zn//0.5 mol L<sup>−1</sup> + Zn(CH<sub>3</sub>COO)<sub>2</sub>//Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> cell charge/discharge curves [<a href="#B42-molecules-29-04929" class="html-bibr">42</a>]; Copyright © 2022, under exclusive license to Springer-Verlag GmbH Germany, part of Springer Nature, Germany (<b>d</b>) Cycling stability of Li<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> cathode with different electrolytes; Copyright© 2016 Elsevier Ltd. All rights reserved. the Netherlands (<b>e</b>) Rate capability of LiFePO<sub>4</sub> tested in the range of 0.5 to 20 C [<a href="#B43-molecules-29-04929" class="html-bibr">43</a>]; Copyright© 2024 Copyright Clearance Center, Inc. All rights reserved, United Kingdom of Great Britain and Northern Ireland (<b>f</b>) Cycling performance at 500 mA·g<sup>−1</sup> in the potential range of Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub>@C of 0.4~2.0 V [<a href="#B17-molecules-29-04929" class="html-bibr">17</a>]. Copyright© 2021, American Chemical Society, American (<b>g</b>) The operando synchrotron XRD patterns of the hybrid Zn-LiFePO<sub>4</sub> (left) and the corresponding charge–discharge curve (right) [<a href="#B43-molecules-29-04929" class="html-bibr">43</a>]. (<b>h</b>) Contour plots of the operando synchrotron XRD data, 15.5–16.5°, in which the (131) peak of LiFePO<sub>4</sub> is converted to the (311) peak of FePO<sub>4</sub> during the initial charge process [<a href="#B43-molecules-29-04929" class="html-bibr">43</a>]. Copyright© 2024 Copyright Clearance Center, Inc. All rights reserved, United Kingdom of Great Britain and Northern Ireland.</p>
Full article ">Figure 4
<p>(<b>a</b>) Charge/discharge curves at different rates in the first cycle; Copyright© 2017, American Chemical Society, American (<b>b</b>) Charge/discharge curves of Li<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> during different cycles; Copyright© 2022, American Chemical Society, American (<b>c</b>) Charge/discharge curves of Zn/Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>2</sub>F<sub>3</sub> at 0.3 C; Copyright© 2020, American Chemical Society, American (<b>d</b>) Cycling performance of Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>2</sub>F<sub>3</sub>/C in non-aqueous zinc-ion batteries at 0.3 C; Copyright© 2020, American Chemical Society. (<b>e</b>) Cycling stability of Zn<sub>3</sub>V<sub>4</sub>(PO<sub>4</sub>)<sub>6</sub> starting from the second cycle at 0.04 Ag<sup>−1</sup> @C/30%BP cycle stability [<a href="#B48-molecules-29-04929" class="html-bibr">48</a>]; Copyright© 2022, American Chemical Society, American (<b>f</b>) Specific capacity and coulombic efficiency obtained at different specific currents [<a href="#B49-molecules-29-04929" class="html-bibr">49</a>]. Copyright © 2020 American Chemical Society, American (<b>g</b>–<b>l</b>) Corresponding SEM images and P:V ratios collected by EDX at the 2nd (<b>g</b>,<b>j</b>), 5th (<b>h</b>,<b>k</b>), and 20th (<b>i</b>,<b>l</b>) cycle; Copyright© 2022, American Chemical Society, American.</p>
Full article ">Figure 5
<p>(<b>a</b>) First charge/discharge curves of Zn/VOPO<sub>4</sub>-based batteries with different electrolytes; Copyright© 2019 Wiley-VCH Verlag GmbH &amp; Co. KGaA, Weinheim, Germany. (<b>b</b>) Cycling performance of batteries employing the electrolyte in different voltage windows of 21 M LiTFSI/1 m Zn(Tr)<sub>2</sub>; Copyright© 2019 Wiley-VCH Verlag GmbH &amp; Co. KGaA, Weinheim, Germany. (<b>c</b>) Charge/discharge curves of Zn asymmetric cells with Ti||1 mA<sup>−2</sup> at 70 PEG [<a href="#B34-molecules-29-04929" class="html-bibr">34</a>]; Copyright© 2022, American Chemical Society, Washington, WA, USA. (<b>d</b>) Cycling stability and Coulombic efficiency of a full cell with electrolyte with or without PEO additive, 1 M ZnSO<sub>4</sub> in 0.5 C [<a href="#B51-molecules-29-04929" class="html-bibr">51</a>]; Copyright© 2020 Wiley-VCH GmbH. (<b>e</b>) In situ XRD patterns of VOPO4/SWCNT electrodes; Copyright© 2019 Wiley-VCH Verlag GmbH &amp; Co. KGaA, Weinheim, Germany.</p>
Full article ">Figure 6
<p>Flow chart of zinc battery to energy storage power station.</p>
Full article ">
14 pages, 1578 KiB  
Article
A Platform of Federated Learning Management for Enhanced Mobile Collaboration
by Farkhod Yusubov and KangYoon Lee
Electronics 2024, 13(20), 4104; https://doi.org/10.3390/electronics13204104 (registering DOI) - 18 Oct 2024
Abstract
Federated learning (FL) has emerged as a crucial technology in today’s data-centric environment, enabling decentralized machine learning while safeguarding user privacy. This study introduces “Federated Learning ML Operations (FedOps) Mobile”, a novel FL framework optimized for the dynamic and heterogeneous ecosystem of mobile [...] Read more.
Federated learning (FL) has emerged as a crucial technology in today’s data-centric environment, enabling decentralized machine learning while safeguarding user privacy. This study introduces “Federated Learning ML Operations (FedOps) Mobile”, a novel FL framework optimized for the dynamic and heterogeneous ecosystem of mobile devices. FedOps Mobile addresses the inherent challenges of FL—such as system scalability, device heterogeneity, and operational efficiency—through advanced on-device training using TensorFlow Lite and CoreML. The framework’s innovative approach includes sophisticated client selection mechanisms that assess device readiness and capabilities, ensuring equitable and efficient participation across the network. Additionally, FedOps Mobile leverages remote device control for seamless task management and continuous learning, all without compromising the user experience. The main contribution of this study is the demonstration that federated learning across heterogeneous devices, especially those using different operating systems, can be both practical and efficient using the FedOps Mobile framework. This was validated through experiments that evaluated three key areas: operational efficiency, model personalization, and resource optimization in multi-device settings. The results showed that the proposed method excels in client selection, energy consumption, and model optimization, establishing a new benchmark for federated learning in diverse and complex environments. Full article
Show Figures

Figure 1

Figure 1
<p>Architecture of FedOps. 1. Platform manager—manages device-specific functionalities and ensures seamless integration and operation of various system components. 2. Network Manager-handles all network-related functionalities, such as registering the client with the FL server and managing network communication. 3. Native Platforms implements machine learning functions, such as Fit(), Evaluate(), and Get weights(), that are crucial for training and evaluating models on the client device. 4. Server side (Microk8s Environment), hosted in a Microk8s environment, plays a pivotal role in managing and coordinating the FL process. 5. FL server, central to the FL process, is the aggregation of models and data analysis. 6. Server Manager manages the overall server operations, including client performance monitoring and data management.</p>
Full article ">Figure 2
<p>Explanation of how FedOps Mobile works after installing the application on mobile. 1. The system administrator registers a new task by sending an FCM message. 2. The online devices send resource information to the FRD. 3. The client selection function is triggered to select devices based on the client selection algorithm 4. Selected device identifications are sent to the FCM. 5. The FCM sends a new message to call selected devices for training. 6. Selected devices connect to the server to obtain the initial global model. 7. The server gives the initial global model to the devices.</p>
Full article ">Figure 3
<p>Performance Increase (Accuracy) Across Rounds for Each Experiment.</p>
Full article ">Figure 4
<p>Energy Consumption Over Rounds for Each Experiment.</p>
Full article ">
19 pages, 2417 KiB  
Article
Modification of 316L Stainless Steel, Nickel Titanium, and Cobalt Chromium Surfaces by Irreversible Immobilization of Fibronectin: Towards Improving the Coronary Stent Biocompatibility
by Hesam Dadafarin, Evgeny Konkov, Hojatollah Vali, Irshad Ali and Sasha Omanovic
Molecules 2024, 29(20), 4927; https://doi.org/10.3390/molecules29204927 (registering DOI) - 18 Oct 2024
Abstract
An extracellular matrix protein, fibronectin (Fn), was covalently immobilized on 316L stainless steel, L605 cobalt chromium (CoCr), and nickel titanium (NiTi) surfaces through an 11-mercaptoundecanoic acid (MUA) self-assembled monolayer (SAM) pre-formed on these surfaces. Polarization modulation infrared reflection adsorption spectroscopy (PM-IRRAS) confirmed the [...] Read more.
An extracellular matrix protein, fibronectin (Fn), was covalently immobilized on 316L stainless steel, L605 cobalt chromium (CoCr), and nickel titanium (NiTi) surfaces through an 11-mercaptoundecanoic acid (MUA) self-assembled monolayer (SAM) pre-formed on these surfaces. Polarization modulation infrared reflection adsorption spectroscopy (PM-IRRAS) confirmed the presence of Fn on the surfaces. The Fn monolayer attached to the SAM was found to be stable under fluid shear stress. Deconvolution of the Fn amide I band indicated that the secondary structure of Fn changes significantly upon immobilization to the SAM-functionalized metal substrate. Scanning electron microscopy and energy dispersive X-ray analysis revealed that the spacing between Fn molecules on a modified commercial stent surface is approximately 66 nm, which has been reported to be the most appropriate spacing for cell/surface interactions. Full article
Show Figures

Figure 1

Figure 1
<p>PM-IRRAS spectra of MUA SAM formed on (a) a 316L SS surface, (b) a CoCr surface, and (c) a NiTi surface.</p>
Full article ">Figure 2
<p>Lower wavenumber region of the PM-IRRAS spectra of MUA SAM formed on (<b>a</b>) a CoCr and (<b>b</b>) a NiTi surface: the solid line depicts the MUA response immediately after its formation and rinsing, whereas the dotted line represents the MUA response after treatment in a phosphoric acid solution.</p>
Full article ">Figure 3
<p>PM-IRASS responses of a modified 316L SS surface. The dotted line represents the response of an NHS activated surface, whereas the solid line represents that of an Fn-modified surface. Similar spectra were recorded with modified CoCr and NiTi surfaces (see <a href="#app1-molecules-29-04927" class="html-app">Figure S1 in the Supplemental</a>).</p>
Full article ">Figure 4
<p>Time dependence of the normalized integrated intensity of the amide I vibration of a covalently immobilized Fn on an MUA-modified 316L SS surface before (solid bars) and after (patterned bars) exposure to simulated laminar flow (PBS, pH = 7.4, T = 37 °C, 20.8 mL min<sup>−1</sup>) for 24 and 72 h.</p>
Full article ">Figure 5
<p>Amide I band of Fn deconvoluted into its underlying secondary structure component peaks (thin solid lines). The black dots represent the experimental PM-IRRAS spectrum of Fn chemically attached to a 316L SS surface through an MUA monolayer (<a href="#molecules-29-04927-sch001" class="html-scheme">Scheme 1</a>). The thick solid curve represents the summation of the secondary structure component bands. The secondary structure bands were assigned based on the values presented in <a href="#molecules-29-04927-t001" class="html-table">Table 1</a>.</p>
Full article ">Figure 6
<p>SEM image of a commercial 316L SS coronary stent surface functionalized with Fn covalently attached to the surface through an MUA monolayer and subsequently labeled with a gold conjugated antibody.</p>
Full article ">Figure 7
<p>EDX mapping of the elemental gold nanoparticle distribution on a commercial 316L SS coronary stent’s surface functionalized with Fn covalently bound to it through an MUA monolayer and subsequently labeled with a gold-conjugated antibody.</p>
Full article ">Scheme 1
<p>Covalent immobilization of fibronectin (Fn) onto a 316L stainless steel surface. (1) MUA film formation, (2) formation of COOH-EDC activated complex, (3) replacement of EDC by NHS to form an NHS-terminated film, (4) replacement of NHS with Fn, and (5) final structure of an Fn-modified 316L-SS surface [<a href="#B22-molecules-29-04927" class="html-bibr">22</a>].</p>
Full article ">
15 pages, 15159 KiB  
Article
Apoptosis, Mitochondrial Autophagy, Fission, and Fusion Maintain Mitochondrial Homeostasis in Mouse Liver Under Tail Suspension Conditions
by Lu-Fan Li, Jiao Yu, Rui Li, Shan-Shan Li, Jun-Yao Huang, Ming-Di Wang, Li-Na Jiang, Jin-Hui Xu and Zhe Wang
Int. J. Mol. Sci. 2024, 25(20), 11196; https://doi.org/10.3390/ijms252011196 (registering DOI) - 18 Oct 2024
Abstract
Microgravity can induce alterations in liver morphology, structure, and function, with mitochondria playing an important role in these changes. Tail suspension (TS) is a well-established model for simulating the effects of microgravity on muscles and bones, but its impact on liver function remains [...] Read more.
Microgravity can induce alterations in liver morphology, structure, and function, with mitochondria playing an important role in these changes. Tail suspension (TS) is a well-established model for simulating the effects of microgravity on muscles and bones, but its impact on liver function remains unclear. In the current study, we explored the regulatory mechanisms of apoptosis, autophagy, fission, and fusion in maintaining liver mitochondrial homeostasis in mice subjected to TS for 2 or 4 weeks (TS2 and TS4). The results showed the following: (1) No significant differences were observed in nuclear ultrastructure or DNA fragmentation between the control and TS-treated groups. (2) No significant differences were detected in the mitochondrial area ratio among the three groups. (3) Cysteine aspartic acid-specific protease 3 (Caspase3) activity and the Bcl-2-associated X protein (bax)/B-cell lymphoma-2 (bcl2) ratio were not higher in the TS2 and TS4 groups compared to the control group. (4) dynamin-related protein 1 (DRP1) protein expression was increased, while mitochondrial fission factor (MFF) protein levels were decreased in the TS2 and TS4 groups compared to the control, suggesting stable mitochondrial fission. (5) No significant differences were observed in the optic atrophy 1 (OPA1), mitofusin 1 and 2 (MFN1 and MFN2) protein expression levels across the three groups. (6) Mitochondrial autophagy vesicles were present in the TS2 and TS4 groups, with a significant increase in Parkin phosphorylation corresponding to the duration of the TS treatment. (7) ATP synthase and citrate synthase activities were significantly elevated in the TS2 group compared to the control group but were significantly reduced in the TS4 group compared to the TS2 group. In summary, the coordinated regulation of apoptosis, mitochondrial fission and fusion, and particularly mitochondrial autophagy preserved mitochondrial morphology and contributed to the restoration of the activities of these two key mitochondrial enzymes, thereby maintaining liver mitochondrial homeostasis in mice under TS conditions. Full article
Show Figures

Figure 1

Figure 1
<p>Influence of TS on morphological data in mice. Numerical values are mean ± standard deviation. n = 8. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group. ** <span class="html-italic">p</span> &lt; 0.01 and * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 2
<p>Histological morphology of mouse liver under different TS treatments. (<b>a</b>) Scale = 100 μm. (<b>b</b>) Scale = 20 μm. Arrows point to hepatocytes. Dashed arrows point to sinusoids. # shows vasculature. Cells within square boxes are necrotic liver cells. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group.</p>
Full article ">Figure 3
<p>Ultrastructure of mouse liver tissue and analysis of mitochondrial number and area under different TS treatments. (<b>a</b>) Scale = 1 μm. * shows mitochondrial autophagic vesicles. Arrows point to mitochondria. (<b>b</b>) Scale = 10 μm. # shows liver nucleus. Arrows point to mitochondria. (<b>c</b>) Number of mitochondria. (<b>d</b>) Mitochondrial cross-sectional area. (<b>e</b>) Mitochondrial area ratio. Numerical values are mean ± standard deviation. Fifteen pictures were analyzed in each group. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group. ** <span class="html-italic">p</span> &lt; 0.01 and * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 4
<p>Activities of ATP synthase (<b>a</b>), CS (<b>b</b>), and Caspase3 (<b>c</b>) in mouse liver under different TS treatments. Numerical values are mean ± standard deviation. n = 8. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group. ** <span class="html-italic">p</span> &lt; 0.01.</p>
Full article ">Figure 5
<p>TUNEL staining of mouse liver under different TS treatments. (<b>a</b>) Scale = 20 μm. Arrows point to DNA fragmentation. Blue fluorescence indicates nuclei; green fluorescence indicates DNA fragmentation. (<b>b</b>) Negative control for TUNEL staining of mouse liver. Scale = 20 μm. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group.</p>
Full article ">Figure 6
<p>Expression levels of liver apoptosis-associated proteins in mice under different TS treatments. (<b>a</b>) Representative Western blot gels. (<b>b</b>) Polyacrylamide gel of total protein. (<b>c</b>) Apoptosis-associated protein level. Numerical values are mean ± standard deviation. n = 8. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group. * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 7
<p>Expression levels of mitochondrial fission- and fusion-associated proteins in mice liver mitochondria under different TS treatments. (<b>a</b>) Representative Western blot gels. (<b>b</b>) Polyacrylamide gel of total protein in the liver. (<b>c</b>) Mitochondrial fission-associated protein levels. (<b>d</b>) Expression levels of mitochondrial fusion-associated proteins. Numerical values are mean ± standard deviation. n = 8. CON, control group; TS2, tail suspension 2-week group; and TS4, tail suspension 4-week group. * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 8
<p>Expression levels of autophagy-associated proteins in mouse liver mitochondria under different TS treatments. (<b>a</b>) Representative Western blot gels. (<b>b</b>) Polyacrylamide gel of total protein. (<b>c</b>) Mitochondrial autophagy-associated protein levels. Numerical values are mean ± standard deviation. n = 8. ** <span class="html-italic">p</span> &lt; 0.01 and * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 9
<p>Summary of impact of TS on liver mitochondrial homeostasis in mice. bcl2, B-cell lymphoma-2; bax, Bcl-2-associated X protein; caspase3, cysteine aspartic acid-specific protease 3; MFN1, mitofusin 1; MFN2, mitofusin 2; OPA1, optic atrophy 1; MFF, mitochondrial fission factor; DRP1, dynamin-related protein 1; Parkin, Parkinson disease protein 2; P-Parkin, phosphorylated Parkin; ATP synthase, adenosine triphosphate synthase; and CS, citrate synthase. Yellow represents apoptosis-related proteins. Gray represents mitochondrial fusion-related proteins. Pink represents mitochondrial fission-related proteins. Green represents mitochondrial autophagy-related proteins. Blue represents oxidative phosphorylation-related proteins. Red arrows represent up- or down-regulation in TS2 group. Blue arrows represent up- or down-regulation in TS4 group.</p>
Full article ">
20 pages, 25074 KiB  
Article
Unraveling Magnet Structural Defects in Permanent Magnet Synchronous Machines—Harmonic Diagnosis and Performance Signatures
by Mehdi Abdolmaleki, Pedram Asef and Christopher Vagg
Magnetism 2024, 4(4), 348-367; https://doi.org/10.3390/magnetism4040023 (registering DOI) - 18 Oct 2024
Abstract
Rare-earth-based permanent magnets (PMs) have a vital role in numerous sustainable energy systems, such as electrical machines (EMs). However, their production can greatly harm the environment and their supply chain monopoly presents economic threats. Alternative materials are emerging, but the use of rare-earth [...] Read more.
Rare-earth-based permanent magnets (PMs) have a vital role in numerous sustainable energy systems, such as electrical machines (EMs). However, their production can greatly harm the environment and their supply chain monopoly presents economic threats. Alternative materials are emerging, but the use of rare-earth PMs remains dominant due to their exceptional performance. Damage to magnet structure can cause loss of performance and efficiency, and propagation of cracks in PMs can result in breaking. In this context, prolonging the service life of PMs and ensuring that they remain damage-free and suitable for re-use is important both for sustainability reasons and cost management. This paper presents a new harmonic content diagnosis and motor performance analysis caused by various magnet structure defects or faults, such as cracked or broken magnets. The proposed method is used for modeling the successive physical failure of the magnet structure in the form of crack formation, crack growth, and magnet breakage. A surface-mounted permanent magnet synchronous motor (PMSM) is studied using simulation in Ansys Maxwell software (Version 2023), and different cracks and PM faults are modeled using the two-dimensional finite element method (FEM). The frequency domain simulation results demonstrate the influence of magnet cracks and their propagation on EM performance measures, such as stator current, distribution of magnetic flux density, back EMF, flux linkage, losses, and efficiency. The results show strong potential for application in health monitoring systems, which could be used to reduce the occurrence of in-service failures, thus reducing the usage of rare-earth magnet materials as well as cost. Full article
Show Figures

Figure 1

Figure 1
<p>Cross-sectional presentation of the studied SPMSM.</p>
Full article ">Figure 2
<p>Cross-sectional view of the model in Ansys Maxwell: (<b>a</b>) 2D CAD and (<b>b</b>) meshed model.</p>
Full article ">Figure 3
<p>Proposed methodology to investigate harmonic and performance signatures in motors.</p>
Full article ">Figure 4
<p>Faulty SPMSM associated with fault type A in the 2D FEM environment, (<b>a</b>) CAD modeling, and (<b>b</b>) corresponding flux density distribution.</p>
Full article ">Figure 5
<p>Faulty SPMSM with fault type B using 2D FEM: (<b>a</b>) CAD modeling; (<b>b</b>) flux density distribution.</p>
Full article ">Figure 6
<p>Faulty SPMSM with fault type C using 2D FEM: (<b>a</b>) CAD modeling; (<b>b</b>) flux density distribution.</p>
Full article ">Figure 7
<p>Torque in the time domain in (<b>a</b>) transient and (<b>b</b>) electrical angle rated load states for healthy and faulty motors with A–C faults.</p>
Full article ">Figure 8
<p>Harmonic content analysis using FEM simulation results and rated load states for healthy and faulty motors with A–C faults: (<b>a</b>) FFT of output torque; (<b>b</b>) FFT of stator currents.</p>
Full article ">Figure 9
<p>Comparison of the amplitude of the harmonics (index) appearing in the output torque in healthy and faulty motors, consecutively.</p>
Full article ">Figure 10
<p>Comparison of the amplitude of the harmonics (index) appearing in the stator currents in healthy and faulty motors.</p>
Full article ">Figure 11
<p>The impact of the demagnetization faults for the healthy and faulty motors under faults A–C: (<b>a</b>) the output torque; and (<b>b</b>) total power.</p>
Full article ">Figure 12
<p>Impact of faults on losses of healthy and faulty motors: (<b>a</b>) copper loss; (<b>b</b>) core loss.</p>
Full article ">Figure 13
<p>The changes in the total loss and efficiency of the healthy and faulty motors under faults A–C: (<b>a</b>) total loss; (<b>b</b>) efficiency.</p>
Full article ">Figure 14
<p>Impact analysis of other types of alternative crack faults with depth, width, and different directions across the magnet. (<b>a</b>) depth cracking study; (<b>b</b>) depth and width cracking study; (<b>c</b>) depth and width cracking study in different magnet locations.</p>
Full article ">Figure 15
<p>Two-dimensional CAD models for (<b>a</b>) fault A: impact analysis of crack depth; (<b>b</b>) fault B: impact analysis of crack widths; and (<b>c</b>) fault C: the random cracks with certain sizes across the magnet.</p>
Full article ">Figure 16
<p>Harmonic content analysis using FEM when fault 1 occurs at rated load torque with the faulty SPMSM: (<b>a</b>) harmonic content analysis of output torque using FFT in healthy and faulty states; (<b>b</b>) harmonic content analysis of stator currents under healthy and fault conditions.</p>
Full article ">Figure 17
<p>Harmonic content analysis using FEM when fault 2 occurs at rated load torque with the faulty SPMSM: (<b>a</b>) harmonic content analysis of output torque using FFT in healthy and faulty states; (<b>b</b>) harmonic content analysis of stator currents in healthy and fault states.</p>
Full article ">Figure 18
<p>Harmonic content analysis using FEM when fault 3 occurs in rated load torque with the faulty SPMSM: (<b>a</b>) harmonic content analysis of output torque using FFT in healthy and faulty states; (<b>b</b>) harmonic content analysis of stator currents in healthy and fault states.</p>
Full article ">
16 pages, 337 KiB  
Review
Overview of Antimicrobial Resistant ESKAPEE Pathogens in Food Sources and Their Implications from a One Health Perspective
by Naomi Oyenuga, José Francisco Cobo-Díaz, Avelino Alvarez-Ordóñez and Elena-Alexandra Alexa
Microorganisms 2024, 12(10), 2084; https://doi.org/10.3390/microorganisms12102084 (registering DOI) - 18 Oct 2024
Abstract
Antimicrobial resistance is an increasing societal burden worldwide, with ESKAPEE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter species and Escherichia coli) pathogens overwhelming the healthcare sectors and more recently becoming predominantly a [...] Read more.
Antimicrobial resistance is an increasing societal burden worldwide, with ESKAPEE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter species and Escherichia coli) pathogens overwhelming the healthcare sectors and more recently becoming predominantly a concern for their persistence in food and food industries, including agricultural settings and animal husbandry environments. The aim of this review is to explore the mechanisms by which the ESKAPEE group gained its multidrug resistance profiles, to analyse their occurrence in different foods and other related reservoirs, including water, and to address the current challenges due to their spread within the food production chain. Moreover, the repertoire of surveillance programmes available focused on monitoring their occurrence, common reservoirs and the spread of antimicrobial resistance are described in this review paper. Evidence from the literature suggests that restricting our scope in relation to multidrug resistance in ESKAPEE pathogens to healthcare and healthcare-associated facilities might actually impede unveiling the actual issues these pathogens can exhibit, for example, in food and food-related reservoirs. Furthermore, this review addresses the need for increasing public campaigns aimed at addressing this challenge, which must be considered in our fight against antimicrobial resistance shown by the ESKAPEE group in food and food-related sectors. Full article
(This article belongs to the Section Food Microbiology)
13 pages, 4004 KiB  
Essay
Genome-Wide Identification and Expression Analysis of the PsTPS Gene Family in Pisum sativum
by Hao Yuan, Baoxia Liu, Guwen Zhang, Zhijuan Feng, Bin Wang, Yuanpeng Bu, Yu Xu, Zhihong Sun, Na Liu and Yaming Gong
Horticulturae 2024, 10(10), 1104; https://doi.org/10.3390/horticulturae10101104 (registering DOI) - 18 Oct 2024
Abstract
This study aimed to explore the role of the trehalose-6-phosphate synthase (TPS) gene family in the adaptation of peas to environmental stress. A comprehensive analysis of the PsTPS gene family identified 20 genes with conserved domains and specific chromosomal locations. Phylogenetic [...] Read more.
This study aimed to explore the role of the trehalose-6-phosphate synthase (TPS) gene family in the adaptation of peas to environmental stress. A comprehensive analysis of the PsTPS gene family identified 20 genes with conserved domains and specific chromosomal locations. Phylogenetic analysis delineated evolutionary relationships, while gene structure analysis revealed compositional insights, and motif analysis provided functional insights. Cis-regulatory element identification predicted gene regulation patterns. Tissue-specific and stress-induced expression profiling highlighted eight genes with ubiquitous expression, with PsTPS15 and PsTPS18 displaying elevated expression levels in roots, nodules, and young stems, and PsTPS13 and PsTPS19 expression downregulated in seeds. Transcriptome analysis identified a differential expression of 20 PsTPS genes, highlighting the significance of 14 genes in response to drought and salinity stress. Notably, under drought conditions, the expression of PsTPS4 and PsTPS6 was initially upregulated and then downregulated, whereas that of PsTPS15 and PsTPS19 was downregulated. Salinity stress notably altered the expression of PsTPS4, PsTPS6, and PsTPS19. Taken together, these findings elucidate the regulatory mechanisms of the PsTPS gene family and their potential as genetic targets for enhancing crop stress tolerance. Full article
(This article belongs to the Section Genetics, Genomics, Breeding, and Biotechnology (G2B2))
Show Figures

Figure 1

Figure 1
<p>Chromosomal locations of the <span class="html-italic">PsTPS</span> genes on the seven pea chromosomes. The distribution of <span class="html-italic">PsTPS</span> genes is relatively sparse, and they are not distributed on every chromosome. The highest distribution of <span class="html-italic">PsTPS</span> genes is observed on Chr5, which contains seven genes.</p>
Full article ">Figure 2
<p>Phylogenetic tree incorporating TPS proteins from <span class="html-italic">Pisum sativum</span> L, <span class="html-italic">Arabidopsis</span>, and <span class="html-italic">Glycine max</span>. The tree of the <span class="html-italic">TPS</span> gene family was constructed by the IQ-TREE 2 software (Version 2.2.0) using the maximum likelihood (ML) method with 1000 bootstrap replicates. The color of the outer ring and branches denote <span class="html-italic">TPS</span> subfamilies.</p>
Full article ">Figure 3
<p>The phylogenetic relationship, conserved motifs, and gene structure of <span class="html-italic">PsTPSs</span>. (<b>a</b>) The maximum likelihood (ML) phylogenetic tree of PsTPS proteins was constructed using a full-length sequence with 1000 bootstrap replicates; (<b>b</b>) Distribution of conserved motifs in PsTPS proteins. A total of 10 motifs were predicted, and the scale bar represents 100 aa; (<b>c</b>) Distribution of the TPS domain in PsTPSs; (<b>d</b>) The gene structures of <span class="html-italic">PsTPSs</span>, including introns (black lines) and exons (green rectangles). The scale bar indicates 1000 bp.</p>
Full article ">Figure 4
<p>CREs on the putative promoters of <span class="html-italic">PsTPSs</span>. (<b>a</b>) Distribution of CREs identified in the 2000 bp upstream promoter region of <span class="html-italic">PsTPSs</span>; (<b>b</b>) The number of CREs on the putative promoters of <span class="html-italic">PsTPSs</span>. Numbers in the heatmap represent the number of elements.</p>
Full article ">Figure 5
<p>Syntenic analyses of <span class="html-italic">TPS</span> genes in <span class="html-italic">Pisum sativum</span>, <span class="html-italic">Arabidopsis</span>, <span class="html-italic">G. max</span>. (<b>a</b>) Seven chromosomes from <span class="html-italic">Pisum sativum</span> (Ps1–Ps7) are mapped, with chromosome length expressed as Mb. Lines denote syntenic <span class="html-italic">TPS</span> gene pairs on the chromosomes. (<b>b</b>) The seven chromosomes of <span class="html-italic">Pisum sativum</span> (Ps1–7), five chromosomes of <span class="html-italic">A. thaliana</span> (At1–5), and twenty chromosomes of <span class="html-italic">G. max</span> (Gm1–20) are mapped. Lines represent syntenic <span class="html-italic">TPS</span> gene pairs.</p>
Full article ">Figure 6
<p>Predicted protein–protein interaction networks of PsTPS proteins with other proteins using the STRING tool. Interactions between proteins are represented by gray lines.</p>
Full article ">Figure 7
<p>Expression profiles of the eight <span class="html-italic">PsTPS</span> genes. The color scale from blue to red indicates increasing log2-transformed FPKM values.</p>
Full article ">Figure 8
<p>Transcriptome analysis depicting the expression levels of 14 <span class="html-italic">PsTPS</span> genes in <span class="html-italic">Pisum sativum</span> under drought stress conditions induced by 10%, 20%, and 30% PEG6000 and salt stress induced by 100 mM, 200 mM, and 300 mM NaCl. Each experiment was conducted independently with a minimum of three replicates. “CK_0h” denotes the control group.</p>
Full article ">
18 pages, 4253 KiB  
Article
The D75N and P161S Mutations in the C0-C2 Fragment of cMyBP-C Associated with Hypertrophic Cardiomyopathy Disturb the Thin Filament Activation, Nucleotide Exchange in Myosin, and Actin–Myosin Interaction
by Anastasia M. Kochurova, Evgenia A. Beldiia, Victoria V. Nefedova, Daria S. Yampolskaya, Natalia A. Koubassova, Sergey Y. Kleymenov, Julia Y. Antonets, Natalia S. Ryabkova, Ivan A. Katrukha, Sergey Y. Bershitsky, Alexander M. Matyushenko, Galina V. Kopylova and Daniil V. Shchepkin
Int. J. Mol. Sci. 2024, 25(20), 11195; https://doi.org/10.3390/ijms252011195 (registering DOI) - 18 Oct 2024
Abstract
About half of the mutations that lead to hypertrophic cardiomyopathy (HCM) occur in the MYBPC3 gene. However, the molecular mechanisms of pathogenicity of point mutations in cardiac myosin-binding protein C (cMyBP-C) remain poorly understood. In this study, we examined the effects of the [...] Read more.
About half of the mutations that lead to hypertrophic cardiomyopathy (HCM) occur in the MYBPC3 gene. However, the molecular mechanisms of pathogenicity of point mutations in cardiac myosin-binding protein C (cMyBP-C) remain poorly understood. In this study, we examined the effects of the D75N and P161S substitutions in the C0 and C1 domains of cMyBP-C on the structural and functional properties of the C0-C1-m-C2 fragment (C0-C2). Differential scanning calorimetry revealed that these mutations disorder the tertiary structure of the C0-C2 molecule. Functionally, the D75N mutation reduced the maximum sliding velocity of regulated thin filaments in an in vitro motility assay, while the P161S mutation increased it. Both mutations significantly reduced the calcium sensitivity of the actin–myosin interaction and impaired thin filament activation by cross-bridges. D75N and P161S C0-C2 fragments substantially decreased the sliding velocity of the F-actin-tropomyosin filament. ADP dose-dependently reduced filament sliding velocity in the presence of WT and P161S fragments, but the velocity remained unchanged with the D75N fragment. We suppose that the D75N mutation alters nucleotide exchange kinetics by decreasing ADP affinity to the ATPase pocket and slowing the myosin cycle. Our molecular dynamics simulations mean that the D75N mutation affects myosin S1 function. Both mutations impair cardiac contractility by disrupting thin filament activation. The results offer new insights into the HCM pathogenesis caused by missense mutations in N-terminal domains of cMyBP-C, highlighting the distinct effects of D75N and P161S mutations on cardiac contractile function. Full article
(This article belongs to the Special Issue Research Progress on the Mechanism and Treatment of Cardiomyopathy)
Show Figures

Figure 1

Figure 1
<p>Temperature dependences of excess heat capacity (Cp) monitored by DSC for the WT C0-C2 fragment and C0-C2 fragments with D75N and P161S mutations.</p>
Full article ">Figure 2
<p>Binding of C0-C2 fragments to F-actin. (<b>a</b>) Examples of images of F-actin bound to the flow cell surface at 100 nM, 300 nM, and 500 nM loading concentrations of C0-C2 fragments. (<b>b</b>) The dependence of the mean fluorescence intensity in the microscope field of view on the C0-C2 fragment concentration. The intensity was averaged by 10 fields of view in three experiments. Experimental data (mean ± SD) were fitted using the Hill equation corresponding fits shown as lines.</p>
Full article ">Figure 3
<p>Effects of cMyBP-C mutations in the N-terminal part of cMyBP-C on the actin–myosin interaction. (<b>a</b>) Dependence of the sliding velocity of thin filaments over myosin in the in vitro motility assay on the C0-C2 fragment loading concentration at <span class="html-italic">p</span>Ca4. (<b>b</b>) Calcium dependence of the sliding velocity of thin filaments over myosin. (<b>c</b>) Effect of cMyBP-C mutations on the relationship between the thin filament sliding velocity and myosin concentration at <span class="html-italic">p</span>Ca4. (<b>d</b>) Influence of cMyBP-C mutations on the dependence of the sliding velocity of F-actin–Tpm filaments on myosin concentration. In (<b>a</b>), the experimental data (mean ± SD) are fitted by the logistic function. In (<b>b</b>–<b>d</b>), the data (mean ± SD) are fitted to the Hill equation. The equation parameters are given in <a href="#ijms-25-11195-t001" class="html-table">Table 1</a> and <a href="#ijms-25-11195-t002" class="html-table">Table 2</a>.</p>
Full article ">Figure 4
<p>Effect of saturated Ca<sup>2+</sup> concentration on the sliding velocity of F-actin over myosin in the presence of 500 nM cMyBP-C fragments. The velocity is presented as the mean ± SD. The symbol * indicates the statistically significant difference between the sliding velocity of F-actin at saturating Ca<sup>2+</sup> concentration (+Ca<sup>2+</sup>) from those without Ca<sup>2+</sup> (−Ca<sup>2+</sup>), <span class="html-italic">p</span> &lt; 0.05. Statistical significance was estimated using the Student’s <span class="html-italic">t</span>-test.</p>
Full article ">Figure 5
<p>(<b>a</b>) Dependence of the sliding velocity of thin filaments on the ATP concentration. The experimental data are fitted to the Hill equation. (<b>b</b>) Dependence of the sliding velocity of thin filaments on the ADP concentration. The experimental data (mean ± SD) for 500 nM D75N C0-C2 fragment are fitted by a linear function; experimental data (mean ± SD) for 0 nM WT C0-C2 fragment, 500 nM WT C0-C2 fragment, and 500 nM P161S C0-C2 fragment were fitted to the Hill equation. The values of the ATP and ADP concentration, at which the velocity was half-maximal, are given in <a href="#ijms-25-11195-t003" class="html-table">Table 3</a>.</p>
Full article ">Figure 6
<p>(<b>a</b>) The minimal distance between Glu2, first charged N-terminal residue of C0 domain, and actin surface in MD trajectory. (<b>b</b>,<b>c</b>) Fluctuations of Tpm strands from the actin helix shown as standard deviations of the mean of the azimuthal angles of the residues in two chains of the Tpm strand 1 and 2, respectively, from the actin helix defined by the positions of the K328 residues in the corresponding long pseudo-helical actin strand.</p>
Full article ">
28 pages, 2807 KiB  
Article
The Mechanism of Tendentious Information Dissemination in Cyberspace
by Teng Zong, Bing Chen, Fengsi Wang, Xin Wei, Yibo Liu, Zongmin Hu and Taowei Li
Appl. Sci. 2024, 14(20), 9505; https://doi.org/10.3390/app14209505 (registering DOI) - 18 Oct 2024
Abstract
Cyberspace has evolved into a hub for the dissemination of large amounts of tendentious information, posing significant challenges to the role of mainstream value information. As netizens’ are the main recipients of tendentious information, their personal cognition, attitude, and behavioral ability affect their [...] Read more.
Cyberspace has evolved into a hub for the dissemination of large amounts of tendentious information, posing significant challenges to the role of mainstream value information. As netizens’ are the main recipients of tendentious information, their personal cognition, attitude, and behavioral ability affect their willingness to re-disseminate information, making them an inalienable force in the promotion of information dissemination. Exploring the dissemination mechanism of tendentious information in cyberspace can help to understand the law of information dissemination and predict the trend of information diffusion, which is of great significance to maintaining information security and social stability. However, the existing research has overlooked the potential influence of the attribute characteristics of information in terms of content, and has failed to overcome the methodological constraints of traditional statistical analysis to accurately describe the variables and mechanisms influencing the dissemination of tendentious information at the cognitive level. Therefore, using structural equation modeling, we propose a research index system based on the Theory of Planned Behavior and the characteristics of tendentious information. To this end, confirmatory factor and model fitting analyses were conducted to develop a tendentious information dissemination mechanism model, which we validated through testing and comparative experiments. Path analysis revealed that Attitude Toward Dissemination, Information Dissemination Intention, and Information Dissemination Behavior are the main links in the information dissemination process. Moreover, Information Sentiment Orientation was found to strongly promote the dissemination of tendentious information, while Subject Norm of Dissemination had a minor inhibiting effect. Full article
Show Figures

Figure 1

Figure 1
<p>Theoretical framework for examining the dissemination mechanism of tendentious information.</p>
Full article ">Figure 2
<p>Model hypotheses for researching the mechanism of tendentious information dissemination.</p>
Full article ">Figure 3
<p>Flowchart of tendentious information dissemination analysis.</p>
Full article ">Figure 4
<p>The measurement model (ATD).</p>
Full article ">Figure 5
<p>Final TIDM model.</p>
Full article ">Figure 6
<p>Model comparison based on different modeling theories: (<b>a</b>) based on TIDM and (<b>b</b>) based on TPB.</p>
Full article ">Figure 7
<p>Model comparison based on different modeling methods: (<b>a</b>) based on structural equation modeling and (<b>b</b>) based on traditional statistical modeling.</p>
Full article ">Figure 8
<p>Cross-validation based on different data samples: (<b>a</b>) <span class="html-italic">N</span> = 227 and (<b>b</b>) <span class="html-italic">N</span> = 516.</p>
Full article ">
13 pages, 5291 KiB  
Article
Redesign of a Balance Rehabilitation Device Based on a Parallel Continuum Mechanism
by Francisco J. Campa and Daniel Díaz-Caneja
Machines 2024, 12(10), 735; https://doi.org/10.3390/machines12100735 (registering DOI) - 18 Oct 2024
Abstract
In the present work, a parallel continuum manipulator for trunk rehabilitation tasks for patients who have suffered a stroke was analyzed and redesigned. The manipulator had to perform active assistance exercises for the motor recovery of the patient. Based on this background, a [...] Read more.
In the present work, a parallel continuum manipulator for trunk rehabilitation tasks for patients who have suffered a stroke was analyzed and redesigned. The manipulator had to perform active assistance exercises for the motor recovery of the patient. Based on this background, a series of requirements were defined, which determined the design framework during the modeling of the manipulator. Finally, an improved prototype was built and tested to verify that the model can properly characterize the behavior of the manipulator. Such tests were carried out using a self-made dummy that replicates the simplifying hypotheses and conditions assumed in the mathematical model. Full article
(This article belongs to the Special Issue Dynamics and Optimization of Compliant and Flexible Mechanisms)
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Elements of the trunk motion rehabilitation device. (<b>b</b>) Kinematic diagram.</p>
Full article ">Figure 2
<p>(<b>a</b>) Model of the i = 1 discretized flexible bar for <span class="html-italic">N</span> = 4. (<b>b</b>) Radius of curvature.</p>
Full article ">Figure 3
<p>Manipulator at −20 degrees during exercise A: (<b>a</b>) α = 0. (<b>b</b>) α = 1.</p>
Full article ">Figure 4
<p>Simulation of exercise A: (<b>a</b>) motors torque; (<b>b</b>) motors position.</p>
Full article ">Figure 5
<p>Parasitic forces in X and Y: (<b>a</b>) exercise A; (<b>b</b>) exercise B; (<b>c</b>) exercise C.</p>
Full article ">Figure 6
<p>(<b>a</b>) Reference system on the coupling between motor and bars. (<b>b</b>) Parametrization of the new section.</p>
Full article ">Figure 7
<p>Parasitic forces in X and Y: (<b>a</b>) exercise A; (<b>b</b>) exercise B; (<b>c</b>) exercise C.</p>
Full article ">Figure 8
<p>(<b>a</b>) New design of the bars. (<b>b</b>) New couplings with better orientation of the spherical joints and the uniaxial sensors attached.</p>
Full article ">Figure 9
<p>(<b>a</b>) Fixture designed with the jacket at default position. (<b>b</b>) Maximum tilting around X (20 deg.). (<b>c</b>) Maximum tilting around Y (20 deg.). (<b>d</b>) Maximum rotation around Z (10 deg.).</p>
Full article ">Figure 10
<p>Tilting measured by the inclinometer: (<b>a</b>) exercise A, (<b>b</b>) exercise B and (<b>c</b>) exercise C.</p>
Full article ">Figure 11
<p>Force measured by the uniaxial force sensors in the bars vs. simulated forces: (<b>a</b>) exercise A; (<b>b</b>) exercise B.</p>
Full article ">
7 pages, 1013 KiB  
Case Report
External Carotid Artery Entrapment by the Hyoid Bone Associated with an Atherosclerotic Stenosis of the Internal Carotid Artery
by Grigol Keshelava, Zurab Robakidze and Devi Tsiklauri
Diseases 2024, 12(10), 258; https://doi.org/10.3390/diseases12100258 (registering DOI) - 18 Oct 2024
Abstract
The mechanical compression of an external carotid artery (ECA) is a rare pathology. The compression of the carotid bifurcation can be positional, induced by anatomical elements, or provoked by volumetric formation in the neck area. In this study, we describe a rare case [...] Read more.
The mechanical compression of an external carotid artery (ECA) is a rare pathology. The compression of the carotid bifurcation can be positional, induced by anatomical elements, or provoked by volumetric formation in the neck area. In this study, we describe a rare case of an entrapment of the ECA. A 67-year-old man who had two episodes of transient ischemic attack (TIA) demonstrated by loss of consciousness was transferred to our hospital. Ultrasonography and computed tomography revealed the atherosclerotic stenosis (80%) of a right internal carotid artery (ICA) and, at the same time, entrapment of the right ECA by the elongated right greater horn of the hyoid bone (GHHB). A 1 cm section of the GHHB was resected. After clamping of the carotid arteries, longitudinal arteriotomy and endarterectomy surgeries were performed from the right ICA. At the two months follow-up examination, the patient’s condition was reported as normal, with no episodes of TIA, dysphagia, or pharyngeal discomfort. Full article
Show Figures

Figure 1

Figure 1
<p>(<b>A</b>) CTA reveals the atherosclerotic stenosis of the right ICA and the entrapment of the right ECA by the GHHB. (<b>B</b>) Axial view of the carotid bifurcation. ICA: internal carotid artery; AP: atherosclerotic plaque; GHHB: greater horn of the hyoid bone; and SECA: stump of external carotid artery.</p>
Full article ">Figure 2
<p>(<b>A</b>) Intraoperative photo: surgical exposure of the right carotid arteries and the GHHB. (<b>B</b>) Graphical image shows the relationship between the carotid arteries and the GHHB. ICA: internal carotid artery; GHHB: greater horn of the hyoid bone; and ECA: external carotid artery.</p>
Full article ">
17 pages, 3832 KiB  
Article
Acceleration of Numerical Modeling of Uranium In Situ Leaching: Application of IDW Interpolation and Neural Networks for Solving the Hydraulic Head Equation
by Maksat B. Kurmanseiit, Madina S. Tungatarova, Banu Z. Abdullayeva, Daniar Y. Aizhulov and Nurlan M. Shayakhmetov
Minerals 2024, 14(10), 1043; https://doi.org/10.3390/min14101043 (registering DOI) - 18 Oct 2024
Abstract
The application of In Situ Leaching (ISL) has significantly boosted uranium production in countries like Kazakhstan. Given that hydrodynamic and chemical processes occur underground, mining enterprises worldwide have developed models of reactive transport. However, modeling these complex processes demands considerable computational resources. This [...] Read more.
The application of In Situ Leaching (ISL) has significantly boosted uranium production in countries like Kazakhstan. Given that hydrodynamic and chemical processes occur underground, mining enterprises worldwide have developed models of reactive transport. However, modeling these complex processes demands considerable computational resources. This issue is particularly significant in the context of numerical analyses of mining processes or when modeling production scenarios in uranium mining by the ISL technique, given that a substantial portion of computational resources is allocated to solving the hydraulic head equation. This work aims to explore the applicability of PINNs to accelerate hydrodynamic simulations of the ISL process. The solution of the Poisson equation is accelerated by generating an initial approximation for the iterative method through the application of the Inverse Distance Weighting (IDW) interpolation and PINNs. The impact of various factors, including the computational grid and the spacing between wells, on both the accuracy and efficiency of initial approximation and the overall solution of the elliptic equation are explored. Employing the hydraulic head distribution obtained through PINNs as the initial approximation led to a significant reduction in computation time and a decrease in the number of iterations by a factor of 2.8 to 7.10. Full article
(This article belongs to the Section Mineral Processing and Extractive Metallurgy)
Show Figures

Figure 1

Figure 1
<p>In-Situ Leaching process involves injection of leaching solution into subsoil (green arrows) and recovery of pregnant solution into the surface (yellow arrows).</p>
Full article ">Figure 2
<p>Calculation domain (<b>a</b>) and distribution of hydraulic pressure (<b>b</b>) at a distance between wells of 50 m.</p>
Full article ">Figure 3
<p>Dependence of mean value on grid size.</p>
Full article ">Figure 4
<p>Distributions of hydraulic head determined by the IDW interpolation method with <math display="inline"><semantics> <mrow> <mi>p</mi> <mspace width="3.33333pt"/> <mo>=</mo> <mspace width="3.33333pt"/> <mn>2</mn> </mrow> </semantics></math> (<b>a</b>) and the iterative SOR method (<b>b</b>) at a distance between wells of 50 m.</p>
Full article ">Figure 5
<p>Resulting number of iterations from various initial approximations used to calculate hydraulic head distribution at various power parameters <span class="html-italic">p</span> and distances between wells (101 × 101 grid dimensions).</p>
Full article ">Figure 6
<p>Initial approximation of hydraulic head determined by the IDW interpolation method with <span class="html-italic">p</span> = 1.47 (<b>a</b>) and the iterative SOR method (<b>b</b>) with the distance between wells of 50 m.</p>
Full article ">Figure 7
<p>Dependence of the number of iterations on power parameter <span class="html-italic">p</span> in IDW method for the computational grids of 151 × 151 (<b>a</b>) and 201 × 201 (<b>b</b>) for different values of the distances between wells.</p>
Full article ">Figure 8
<p>Physics-Informed Neural Network (PINN) algorithm architecture.</p>
Full article ">Figure 9
<p>Distribution of the initial approximation of the hydraulic head determined by the PINN method (<b>a</b>) and the distribution of the hydrodynamic head calculated by the iterative SOR method (<b>b</b>) on a 101 × 101 computational grid with a distance between wells of 50 m.</p>
Full article ">Figure 10
<p>Initial approximation for hydraulic head distribution defined by PINNs (<b>a</b>) and hydraulic head calculated by SOR method (<b>b</b>) for a distance of 30 m between wells.</p>
Full article ">Figure 11
<p>Initial approximation for hydraulic head distribution defined by PINNs (<b>a</b>) and hydraulic head calculated by SOR method (<b>b</b>) for a distance of 40 m between wells.</p>
Full article ">Figure 12
<p>Initial approximation for hydraulic head distribution defined by PINNs (<b>a</b>) and hydraulic head calculated by SOR method (<b>b</b>) for a distance of 60 m between wells.</p>
Full article ">Figure 13
<p>Initial approximation for hydraulic head distribution defined by PINNs (<b>a</b>) and hydraulic head calculated by SOR method (<b>b</b>) for a distance of 70 m between wells.</p>
Full article ">Figure 14
<p>Dependence of computation time on learning rate and number of epochs.</p>
Full article ">Figure 15
<p>Dependence of the maximum calculation error on the learning rate and the number of epochs.</p>
Full article ">Figure 16
<p>Distribution of hydrodynamic pressure along the diagonal line, determined by the iterative method (red line), and initial approximations defined by interpolation IDW with power parameters <math display="inline"><semantics> <mrow> <mi>p</mi> <mspace width="3.33333pt"/> <mo>=</mo> <mspace width="3.33333pt"/> <mn>2</mn> </mrow> </semantics></math> (orange line), <math display="inline"><semantics> <mrow> <mi>p</mi> <mspace width="3.33333pt"/> <mo>=</mo> <mspace width="3.33333pt"/> <mn>1.47</mn> </mrow> </semantics></math> (green line) and by PINNs (blue line) on computational mesh 101 × 101.</p>
Full article ">Figure 17
<p>Distribution of hydrodynamic pressure along the diagonal line, determined by the iterative method (red line), and initial approximations defined by interpolation IDW (green line) and by PINNs (blue line) with power parameter <math display="inline"><semantics> <mrow> <mi>p</mi> <mspace width="3.33333pt"/> <mo>=</mo> <mspace width="3.33333pt"/> <mn>0.56</mn> </mrow> </semantics></math> for calculation mesh 151 × 151 (<b>a</b>) and <math display="inline"><semantics> <mrow> <mi>p</mi> <mo>=</mo> <mn>0.3</mn> </mrow> </semantics></math> for mesh 201 × 201 (<b>b</b>).</p>
Full article ">
Back to TopTop