Nothing Special   »   [go: up one dir, main page]

You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
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

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (2,039)

Search Parameters:
Keywords = stress map

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
25 pages, 7960 KiB  
Article
Effectiveness Analysis of the Non-Standard Reinforcement of Lattice Tower Legs Using the Component-Based Finite Element Method
by Jacek Szafran, Klaudia Juszczyk-Andraszyk and Paulina Kaszubska
Materials 2025, 18(6), 1242; https://doi.org/10.3390/ma18061242 (registering DOI) - 11 Mar 2025
Abstract
This paper presents an analysis of the effectiveness of the existing reinforcement of steel lattice tower legs made of L-sections by expanding to closely spaced built-up members. Due to the significant differences between the standard assumptions and the existing reinforcement, numerical analyses based [...] Read more.
This paper presents an analysis of the effectiveness of the existing reinforcement of steel lattice tower legs made of L-sections by expanding to closely spaced built-up members. Due to the significant differences between the standard assumptions and the existing reinforcement, numerical analyses based on the component-based finite element method (CBFEM) were used to estimate the capacity of the existing structure’s tower legs. Geometrically and materially nonlinear stress analysis and linear buckling analysis were performed. The obtained results (stress distribution maps, buckling forms, and corresponding critical forces) were used to modify the geometric parameters of the section of the analyzed tower legs in order to adapt the standard formulas in the calculation procedure. In the analyzed case, distance of the connections between the branches exceeded that indicated in EN 1993-1-1:2005 for the condition concerning the possibility of ignoring the deformation susceptibility in the calculation process. However, it did not result in the separate operation of each branch of the section. Thus, in the case of the analyzed reinforcement, it is possible to neglect the form susceptibility when calculating the buckling resistance of the element. The buckling capacity of the reinforced legs of the tower and the compression capacity of the section of the analyzed structure were calculated according to the method that took into account the results of the numerical analyses. These values are about 35–48% and 30–39% higher, respectively, than the capacity of the unreinforced angle calculated according to EN 1993-1-1:2005 and EN 1993-1-8:2006 standards. Thus, it may be possible to avoid costly and labor-intensive retrofitting of the existing reinforcement to meet the standard requirements. A key issue, and one that is particularly important in light of the lack of standard guidelines aimed at designing reinforcements for telecommunications structures, seems to be the performance of full-scale experimental tests. Full article
Show Figures

Figure 1

Figure 1
<p>The analyzed structure: (<b>a</b>) view of the tower; (<b>b</b>) a schematic of the structure.</p>
Full article ">Figure 2
<p>The view of the channel–angle connection (<b>top</b>) and cross-section through the reinforced tower leg at the selected location (<b>bottom</b>).</p>
Full article ">Figure 3
<p>Connections of reinforcing elements along the length.</p>
Full article ">Figure 4
<p>Anchoring of reinforcing elements in the foundation.</p>
Full article ">Figure 5
<p>Proximity elements according to the standard [<a href="#B22-materials-18-01242" class="html-bibr">22</a>].</p>
Full article ">Figure 6
<p>Connections at the ends of the tower leg: (<b>a</b>) bottom; (<b>b</b>) top.</p>
Full article ">Figure 7
<p>Computational models that do not include elements. (<b>A</b>) Model A (<b>B</b>) Model B (<b>C</b>) Model C (<b>D</b>) Model D.</p>
Full article ">Figure 8
<p>Computational model considering the lattice element.</p>
Full article ">Figure 9
<p>Mesh—general view (<b>top</b>), details (<b>bottom</b>).</p>
Full article ">Figure 10
<p>Material model in MNA and GMNIA analyses.</p>
Full article ">Figure 11
<p>Model A: equivalent stresses; GMNIA analysis—general view (left), close-ups on the element (center), close-ups on connections (right).</p>
Full article ">Figure 12
<p>Model B: equivalent stresses; GMNIA analysis—general view (left), close-ups on the element (center), close-ups on connections (right).</p>
Full article ">Figure 13
<p>Model C: equivalent stresses; GMNIA analysis—general view (left), close-ups on the element (center), close-ups on connections (right).</p>
Full article ">Figure 14
<p>Model D: equivalent stresses; GMNIA analysis—general view (left), close-ups on the element (center), close-ups on connections (right).</p>
Full article ">Figure 15
<p>Model E: equivalent stresses; GMNIA analysis—general view (left), close-ups on the element (center), close-ups on connections (right).</p>
Full article ">
27 pages, 10720 KiB  
Article
Evaluation of the Sensitivity of PBL and SGS Treatments in Different Flow Fields Using the WRF-LES at Perdigão
by Erkan Yılmaz, Şükran Sibel Menteş and Gokhan Kirkil
Energies 2025, 18(6), 1372; https://doi.org/10.3390/en18061372 - 11 Mar 2025
Viewed by 27
Abstract
This study investigates the effectiveness of the large eddy simulation version of the Weather Research and Forecasting model (WRF-LES) in reproducing the atmospheric conditions observed during a Perdigão field experiment. When comparing the results of the WRF-LES with observations, using LES settings can [...] Read more.
This study investigates the effectiveness of the large eddy simulation version of the Weather Research and Forecasting model (WRF-LES) in reproducing the atmospheric conditions observed during a Perdigão field experiment. When comparing the results of the WRF-LES with observations, using LES settings can accurately represent both large-scale events and the specific characteristics of atmospheric circulation at a small scale. Six sensitivity experiments are performed to evaluate the impact of different planetary boundary layer (PBL) schemes, including the MYNN, YSU, and Shin and Hong (SH) PBL models, as well as large eddy simulation (LES) with Smagorinsky (SMAG), a 1.5-order turbulence kinetic energy closure (TKE) model, and nonlinear backscatter and anisotropy (NBA) subgrid-scale (SGS) stress models. Two case studies are selected to be representative of flow conditions. In the northeastern flow, the MYNN NBA simulation yields the best result at a height of 100 m with an underestimation of 3.4%, despite SH generally producing better results than PBL schemes. In the southwestern flow, the MYNN TKE simulation at station Mast 29 is the best result, with an underestimation of 1.2%. The choice of SGS models over complex terrain affects wind field features in the boundary layer more than above the boundary layer. The NBA model generally produces better results in complex terrain when compared to other SGS models. In general, the WRF-LES can model the observed flow with high-resolution topographic maps in complex terrain with different SGS models for both flow regimes. Full article
(This article belongs to the Special Issue Computational and Experimental Fluid Dynamics for Wind Energy)
Show Figures

Figure 1

Figure 1
<p>Perdigão terrain.</p>
Full article ">Figure 2
<p>Topography of domains used in the multiscale simulation. The three domains had resolutions of 5000 m as d01 (the coarsest corresponding to the entire domain), d02 and d03 (the finest), 1000 m, and 100 m.</p>
Full article ">Figure 3
<p>Taylor diagram of 100 m northeastern flow wind speeds at Mast 20 (blue dot) and Mast 29 (red dot), comparing observations with simulation results for 3 different PBL parameters in (I) MYNN PBL scheme, (II) SH PBL scheme, and (III) YSU PBL scheme for D02 domain.</p>
Full article ">Figure 4
<p>Average horizontal wind velocity and vertical wind component for 3 different PBL parameters and 3 different LES schemes of northeast flow: (I) MYNN PBL scheme, (II) YSU PBL scheme, and (III) SH PBL scheme for D03 domain. First column is horizontal wind velocity at 10 m, second column is vertical wind component at 10 m, third column is horizontal wind velocity at 100 m, and fourth column is vertical wind component at 100 m for d03 domain area. First lines of each PBL parameterization are TKE model results, second lines are SMAG model results, and third lines are NBA model results.</p>
Full article ">Figure 5
<p>Transect of one-day time-averaged along-transect velocity differences from MYNN TKE model results for (<b>a</b>) MYNN TKE model, (<b>b</b>) MYNN SMAG model, (<b>c</b>) MYNN NBA model, (<b>d</b>) YSU TKE model, (<b>e</b>) YSU SMAG model, (<b>f</b>) YSU NBA model, (<b>g</b>) SH TKE model, (<b>h</b>) SH SMAG model, and (<b>i</b>) SH NBA model for northeastern flow.</p>
Full article ">Figure 6
<p>Time series graphs and comparisons of simulated and observed wind speeds at 100 m for northeastern flow. First column shows MYNN results, second column shows YSU results, and third column shows SH results. First row is Mast 20, second row is Mast 25, and third row is Mast 29 results. Black lines represent measurements, green lines TKE simulations, blue lines SMAG simulations, and red lines NBA simulations.</p>
Full article ">Figure 7
<p>Wind speed bias results of comparisons of simulated and observed data vertical profiles for northeastern flow at (<b>a</b>) Mast 20, (<b>b</b>) Mast 25, and (<b>c</b>) Mast 29.</p>
Full article ">Figure 8
<p>Taylor diagram of 100 m southwestern flow wind speeds at Mast 20 (blue dot) and Mast 29 (red dot), comparing observations with simulation results for 3 different PBL parameters in (I) MYNN PBL scheme, (II) SH PBL scheme, and (III) YSU PBL scheme for D02 domain.</p>
Full article ">Figure 9
<p>Average horizontal wind velocity and vertical wind component for 3 different PBL parameters and 3 different LES schemes of southwestern flow: (I) MYNN PBL scheme, (II) YSU PBL scheme, and (III) SH PBL scheme. First columns are horizontal wind velocity at 10 m, second columns are vertical wind component at 10 m, third columns are horizontal wind velocity at 100 m, and fourth columns are vertical wind component at 100 m for d03 domain area. First line is TKE model results, second line is SMAG model results, and third line is NBA model results.</p>
Full article ">Figure 10
<p>Transect of one-day time-averaged along-transect velocity difference from MYNN TKE model results (<b>a</b>) MYNN TKE model, (<b>b</b>) MYNN SMAG model, (<b>c</b>) MYNN NBA model, (<b>d</b>) YSU TKE model, (<b>e</b>) YSU SMAG model, (<b>f</b>) YSU NBA model, (<b>g</b>) SH TKE model, (<b>h</b>) SH SMAG model, and (<b>i</b>) SH NBA model for southwestern flow.</p>
Full article ">Figure 11
<p>Time series graphs and comparisons of simulated and observed wind speeds at 100 m for southwestern flow. First column shows MYNN results, second column shows YSU results, and third column shows SH results. First row is Mast 20, second row is Mast 25, and third row is Mast 29 results. Black lines represent measurements, green lines TKE simulations, blue lines SMAG simulations, and red lines NBA simulations.</p>
Full article ">Figure 12
<p>Wind speed bias results of comparisons of simulated and observed data vertical profiles for southwestern flow at (<b>a</b>) Mast 20, (<b>b</b>) Mast 25, and (<b>c</b>) Mast 29.</p>
Full article ">Figure 13
<p>Daily diurnal wind speeds at 100 m of (<b>a</b>) northeastern flow at Mast 20, (<b>b</b>) southwestern flow at Mast 20, (<b>c</b>) northeastern flow at Mast 25, (<b>d</b>) southwestern flow at Mast 25, (<b>e</b>) northeastern flow at Mast 29, and (<b>f</b>) southwestern flow at Mast 29. Box plots include entire time period of study.</p>
Full article ">Figure 14
<p>Comparison of spectra between Mast 20 and WRF-LES d03 domain (Δx = 100 m) results for MYNN parameter and d02 domain (Δx = 1000 m).</p>
Full article ">
33 pages, 2472 KiB  
Review
Multi-Omics Approaches Against Abiotic and Biotic Stress—A Review
by Venkatramanan Varadharajan, Radhika Rajendran, Pandiyan Muthuramalingam, Ashish Runthala, Venkatesh Madhesh, Gowtham Swaminathan, Pooja Murugan, Harini Srinivasan, Yeonju Park, Hyunsuk Shin and Manikandan Ramesh
Plants 2025, 14(6), 865; https://doi.org/10.3390/plants14060865 - 10 Mar 2025
Viewed by 264
Abstract
Plants face an array of environmental stresses, including both abiotic and biotic stresses. These stresses significantly impact plant lifespan and reduce agricultural crop productivity. Abiotic stresses, such as ultraviolet (UV) radiation, high and low temperatures, salinity, drought, floods, heavy metal toxicity, etc., contribute [...] Read more.
Plants face an array of environmental stresses, including both abiotic and biotic stresses. These stresses significantly impact plant lifespan and reduce agricultural crop productivity. Abiotic stresses, such as ultraviolet (UV) radiation, high and low temperatures, salinity, drought, floods, heavy metal toxicity, etc., contribute to widespread crop losses globally. On the other hand, biotic stresses, such as those caused by insects, fungi, and weeds, further exacerbate these challenges. These stressors can hinder plant systems at various levels, including molecular, cellular, and development processes. To overcome these challenges, multi-omics computational approaches offer a significant tool for characterizing the plant’s biomolecular pool, which is crucial for maintaining homeostasis and signaling response to environmental changes. Integrating multiple layers of omics data, such as proteomics, metabolomics, ionomics, interactomics, and phenomics, simplifies the study of plant resistance mechanisms. This comprehensive approach enables the development of regulatory networks and pathway maps, identifying potential targets for improving resistance through genetic engineering or breeding strategies. This review highlights the valuable insights from integrating multi-omics approaches to unravel plant stress responses to both biotic and abiotic factors. By decoding gene regulation and transcriptional networks, these techniques reveal critical mechanisms underlying stress tolerance. Furthermore, the role of secondary metabolites in bio-based products in enhancing plant stress mitigation is discussed. Genome editing tools offer promising strategies for improving plant resilience, as evidenced by successful case studies combating various stressors. On the whole, this review extensively discusses an advanced multi-omics approach that aids in understanding the molecular basis of resistance and developing novel strategies to improve crops’ or organisms’ resilience to abiotic and biotic stresses. Full article
Show Figures

Figure 1

Figure 1
<p>Omics approaches to studying plant stress response.</p>
Full article ">Figure 2
<p>Gene regulation against abiotic/biotic stresses.</p>
Full article ">Figure 3
<p>Use of CRISPR/CAS9 in crop improvement against abiotic/biotic stresses. (1) Tomato leaf curl disease, (2) powdery mildew infection in wheat plant, (3) rice plant infested with <span class="html-italic">Xanthomonas oryzae,</span> (4) drought, (5) high salinity, and (6) high temperature.</p>
Full article ">Figure 4
<p>Applications of ZFN and TALEN on plants against abiotic/biotic stresses: (1) resistance against viruses in maize, (2) resistance of plants to heavy metals, (3) high-yield crops, and (4) herbicide resistance plant.</p>
Full article ">
18 pages, 12151 KiB  
Article
LGR-Net: A Lightweight Defect Detection Network Aimed at Elevator Guide Rail Pressure Plates
by Ruizhen Gao, Meng Chen, Yue Pan, Jiaxin Zhang, Haipeng Zhang and Ziyue Zhao
Sensors 2025, 25(6), 1702; https://doi.org/10.3390/s25061702 - 10 Mar 2025
Viewed by 181
Abstract
In elevator systems, pressure plates secure guide rails and limit displacement, but defects compromise their performance under stress. Current detection algorithms face challenges in achieving high localization accuracy and computational efficiency when detecting small defects in guide rail pressure plates. To overcome these [...] Read more.
In elevator systems, pressure plates secure guide rails and limit displacement, but defects compromise their performance under stress. Current detection algorithms face challenges in achieving high localization accuracy and computational efficiency when detecting small defects in guide rail pressure plates. To overcome these limitations, this paper proposes a lightweight defect detection network (LGR-Net) for guide rail pressure plates based on the YOLOv8n algorithm. To solve the problem of excessive model parameters in the original algorithm, we enhance the baseline model’s backbone network by incorporating the lightweight MobileNetV3 and optimize the neck network using the Ghost convolution module (GhostConv). To improve the localization accuracy for small defects, we add a high-resolution small object detection layer (P2 layer) and integrate the Convolutional Block Attention Module (CBAM) to construct a four-scale feature fusion network. This study employs various data augmentation methods to construct a custom dataset for guide rail pressure plate defect detection. The experimental results show that LGR-Net outperforms other YOLO-series models in terms of overall performance, achieving optimal results in terms of precision (p = 98.7%), recall (R = 98.9%), mAP (99.4%), and parameter count (2,412,118). LGR-Net achieves low computational complexity and high detection accuracy, providing an efficient and effective solution for defect detection in elevator guide rail pressure plates. Full article
(This article belongs to the Section Sensing and Imaging)
Show Figures

Figure 1

Figure 1
<p>Schematic diagram of the guide rail clamp.</p>
Full article ">Figure 2
<p>YOLOv8 network architecture diagram.</p>
Full article ">Figure 3
<p>LGR-Net network structure.</p>
Full article ">Figure 4
<p>CBAM structure. Where ⊗ denotes element-wise multiplication.</p>
Full article ">Figure 5
<p>CAM structure. <span class="html-fig-inline" id="sensors-25-01702-i001"><img alt="Sensors 25 01702 i001" src="/sensors/sensors-25-01702/article_deploy/html/images/sensors-25-01702-i001.png"/></span> represents element-wise addition and the application of the activation function sigmoid, respectively.</p>
Full article ">Figure 6
<p>SAM structure. <span class="html-fig-inline" id="sensors-25-01702-i002"><img alt="Sensors 25 01702 i002" src="/sensors/sensors-25-01702/article_deploy/html/images/sensors-25-01702-i002.png"/></span> represents the activation function Sigmoid.</p>
Full article ">Figure 7
<p>MobileNetV3 structure.</p>
Full article ">Figure 8
<p>GhostConv structure.</p>
Full article ">Figure 9
<p>Defect types.</p>
Full article ">Figure 10
<p>Images after data augmentation.</p>
Full article ">Figure 11
<p>LGR-Net training results.</p>
Full article ">Figure 12
<p>Visualization of ablation experiment data. ((A)—YOLOv8n, (B)—YOLOv8n + i, (C)—YOLOv8n + ii, (D)—YOLOv8n + i + ii, (E)—YOLOv8n + i +ii + iii, (F)—LGR-Net).</p>
Full article ">Figure 13
<p>Visualization of detection results from ablation experiments.</p>
Full article ">Figure 14
<p>Detection results for small hole defects.</p>
Full article ">Figure 15
<p>Detection results for scratch defects.</p>
Full article ">Figure 16
<p>Detection results for crack defects.</p>
Full article ">Figure 17
<p>Detection results for wear defects.</p>
Full article ">Figure 18
<p>LGR-Net deployment demonstration.</p>
Full article ">
23 pages, 10348 KiB  
Article
Genome-Wide Identification of the SWEET Gene Family and Functional Analysis of BraSWEET10 in Winter B. rapa (Brassica rapa L.) Under Low-Temperature Stress
by Jinli Yue, Shunjie Yuan, Lijun Liu, Zaoxia Niu, Li Ma, Yuanyuan Pu, Junyan Wu, Yan Fang and Wancang Sun
Int. J. Mol. Sci. 2025, 26(6), 2398; https://doi.org/10.3390/ijms26062398 - 7 Mar 2025
Viewed by 92
Abstract
Sugars will eventually be exported transporter (SWEET), a class of glucose transport proteins, is crucial in plants for glucose transport by redistribution of sugars and regulates growth, development, and stress tolerance. Although the SWEET family has been studied in many plants, little is [...] Read more.
Sugars will eventually be exported transporter (SWEET), a class of glucose transport proteins, is crucial in plants for glucose transport by redistribution of sugars and regulates growth, development, and stress tolerance. Although the SWEET family has been studied in many plants, little is known about its function in winter B. rapa (Brassica rapa L.). Bioinformatics approaches were adopted to identify the SWEET gene (BraSWEETs) family in B. rapa to investigate its role during overwintering. From the whole-genome data, 31 BraSWEET genes were identified. Gene expansion was realized by tandem and fragment duplication, and the 31 genes were classified into four branches by phylogenetic analysis. As indicated by exon–intron structure, cis-acting elements, MEME (Multiple EM for Motif Elicitation) motifs, and protein structure, BraSWEETs were evolutionarily conserved. According to the heat map, 23 BraSWEET genes were differentially expressed during overwintering, revealing their potential functions in response to low-temperature stress and involvement in the overwintering memory-formation mechanism. BraSWEET10 is mainly associated with plant reproductive growth and may be crucial in the formation of overwintering memory in B. rapa. The BraSWEET10 gene was cloned into B. rapa (Longyou-7, L7). The BraSWEET10 protein contained seven transmembrane structural domains. Real-time fluorescence quantitative PCR (qRT-PCR) showed that the BraSWEET10 gene responded to low-temperature stress. BraSWEET10 was localized to the cell membrane. The root length of overexpressing transgenic A. thaliana was significantly higher than that of wild-type (WT) A. thaliana under low temperatures. Our findings suggest that this gene may be important for the adaptation of winter B. rapa to low-temperature stress. Overall, the findings are expected to contribute to understanding the evolutionary links of the BraSWEET family and lay the foundation for future studies on the functional characteristics of BraSWEET genes. Full article
(This article belongs to the Collection Advances in Molecular Plant Sciences)
Show Figures

Figure 1

Figure 1
<p>The transmembrane domain of BraSWEET proteins. The blue lines signify the intracellular region. The thick purple line denotes the transmembrane region. Yellow lines indicate the extracellular region.</p>
Full article ">Figure 2
<p>Gene structure and motifs of the <span class="html-italic">BraSWEET</span> genes. (<b>A</b>) The phylogenetic tree of BraSWEET proteins. (<b>B</b>) The exon–intron structure of 31 <span class="html-italic">BraSWEET</span> genes. Exons and introns are represented by rose boxes and blue lines, respectively. (<b>C</b>) The motif composition of BraSWEET proteins. The seven motifs are represented by differently colored rectangles.</p>
Full article ">Figure 3
<p>Phylogenetic tree of SWEET proteins in <span class="html-italic">Brassica rapa</span> L. (L7) and <span class="html-italic">A. thaliana</span>. The numbers on the branches indicate the bootstrap percentage values calculated from 1000 replicates. The genes in the pink, yellow, blue, and green clades are clubbed in Group1, Group2, Group3, and Group4, respectively. The clades containing only <span class="html-italic">AtSWEET</span> genes are marked with a red star. The clade containing only one MtN3 motif is indicated using a green triangle.</p>
Full article ">Figure 4
<p>Chromosomal locations of <span class="html-italic">BraSWEET</span> genes. Black lines represent the gene position on the chromosome. Tandemly duplicated genes are indicated with orange boxes.</p>
Full article ">Figure 5
<p>Synteny analysis for the SWEET family in <span class="html-italic">B. rapa</span> (L7). Gray lines indicate all synteny blocks in the genome of <span class="html-italic">B. rapa</span> (L7). Red lines indicate the duplication of <span class="html-italic">BraSWEET</span> gene pairs.</p>
Full article ">Figure 6
<p>Synteny analysis of SWEET genes in <span class="html-italic">B. rapa</span> (L7), Arabidopsis, and Chinese cabbage. The gray lines in the background represent collinear blocks in genomes of <span class="html-italic">B. rapa</span> (BrapaL7), A. thaliana (ATH), and Chinese cabbage (rapa), and the red lines highlight collinear SWEET gene pairs.</p>
Full article ">Figure 7
<p>Predicted tertiary structure of BraSWEET proteins.</p>
Full article ">Figure 8
<p>Cis-acting elements in the promoter regions of <span class="html-italic">BraSWEETs</span>. Cis-acting elements were identified by PlantCARE using upstream 1500 bp sequences of the <span class="html-italic">BraSWEETs</span>. Red inverted triangle, green inverted triangle, brown square, blue triangle, light blue square, orange inverted triangle, purple square, dark green square, dark red triangle, and red inverted triangle represent <span class="html-italic">ABRE</span>, <span class="html-italic">ARE</span>, <span class="html-italic">DRE</span>, <span class="html-italic">ERE</span>, <span class="html-italic">LTR</span>, <span class="html-italic">MBS</span>, <span class="html-italic">MYB</span>, <span class="html-italic">MYC</span>, and <span class="html-italic">W-Box</span>, respectively. The scale bar on the bottom indicates the length of promoter sequences.</p>
Full article ">Figure 9
<p>Predicted protein–protein interaction network for BraSWEET proteins. The network nodes represent proteins. The line width indicates the reliability of the interaction. The node size represents the number of proteins that interact with each other.</p>
Full article ">Figure 10
<p>Expression profiles of 23 <span class="html-italic">BraSWEWTs</span> genes in different overwintering periods. (<b>A</b>) Heat map of <span class="html-italic">BraSWEWTs</span> genes in six periods of overwintering (S1–S6). (<b>B</b>) Plant growth map in different wintering periods (S1–S6).</p>
Full article ">Figure 11
<p>Subcellular localization of BraSWEET10 in tobacco. Treatment: 20% sucrose, 5–10 min. (<b>A</b>) Fluorescence image for BraSWEET10-GFP. (<b>B</b>) Bright field. (<b>C</b>) Merger of the first two images.</p>
Full article ">Figure 12
<p>Expression level of <span class="html-italic">BraSWEET10</span> in <span class="html-italic">transgenic A. thaliana.</span> WT: wild type, 1#/2#/3#: <span class="html-italic">BraSWEET10</span> transgenic <span class="html-italic">A. thaliana</span>. <sup>a</sup> <span class="html-italic">p</span> &lt; 0.01 vs. WT group, <sup>b</sup> <span class="html-italic">p</span> &lt; 0.05 vs. WT group.</p>
Full article ">Figure 13
<p>Root length of transgenic <span class="html-italic">A. thaliana</span> after low-temperature stress. WT: wild type, 3#: <span class="html-italic">BraSWEET10</span> transgenic <span class="html-italic">A. thaliana.</span> (<b>A</b>) Normal condition culture, (<b>B</b>) low-temperature (4 °C) treatment, (<b>C</b>) root length of <span class="html-italic">A. thaliana</span> plants after low-temperature treatment. <sup>a</sup> <span class="html-italic">p</span> &lt; 0.01, 3# group vs. WT group.</p>
Full article ">
13 pages, 12068 KiB  
Review
The Effect of Leisure-Time Exercise on Mental Health Among Adults: A Bibliometric Analysis of Randomized Controlled Trials
by Karuppasamy Govindasamy, Masilamani Elayaraja, Abderraouf Ben Abderrahman, Koulla Parpa, Borko Katanic and Urs Granacher
Healthcare 2025, 13(5), 575; https://doi.org/10.3390/healthcare13050575 - 6 Mar 2025
Viewed by 136
Abstract
Background: Adequate levels of leisure-time exercise (LTE) are associated with mental health benefits. Despite increased research in recent years through randomized controlled trials (RCTs), a systematic literature review summarizing these findings is lacking. Here, we examined publication trends, impact, and research gaps regarding [...] Read more.
Background: Adequate levels of leisure-time exercise (LTE) are associated with mental health benefits. Despite increased research in recent years through randomized controlled trials (RCTs), a systematic literature review summarizing these findings is lacking. Here, we examined publication trends, impact, and research gaps regarding LTE’s effects on mental health in the form of a bibliometric analysis. Methods: Five electronic databases (PubMed, EMBASE, Web of Science, Ovid Medline, and the Cumulative Index for Nursing and Allied Health Literature) were searched from their inception until 20 November 2024. Citations were independently screened by two authors and included based on pre-determined eligibility criteria. Bibliometric analysis was conducted using SciVal and VOSviewer under five themes: (1) descriptive analysis, (2) network analysis, (3) thematic mapping, (4) co-citation and co-occurrence analysis, and (5) bibliometric coupling. Results: The systematic search identified 5792 citations, of which 78 RCTs met the inclusion criteria. Only one study was conducted in a low- or middle-income country. Sixty-four percent of studies were published in quartile-one journals. Most studies were conducted in the United States, followed by Australia, Canada, and the United Kingdom. National collaborations yielded the highest citation rates, reflecting the influence of cultural and social norms on exercise and mental health. Research gaps were identified with regards to the validity of mental health measures, the paucity of data from low- and middle-income countries, and emerging research sources. Conclusions: This bibliometric analysis highlights the existing evidence on LTE’s impact on mental health and identifies areas for future research and policy. Trials exploring valid mental health outcomes, biomarkers such as mood and oxidative stress, and collaborative research are needed, particularly in underrepresented regions of the world. Full article
(This article belongs to the Special Issue Physical Activity for Promoting Mental Health)
Show Figures

Figure 1

Figure 1
<p>PRISMA flowchart guiding the screening and inclusion of studies for bibliometric analysis.</p>
Full article ">Figure 2
<p>Descriptive analysis of the studies included for the systematic review: (<b>a</b>) shows year-wise number of publications; (<b>b</b>) shows citations across time; (<b>c</b>) shows the publications in different quartiles.</p>
Full article ">Figure 3
<p>Global trends in the number of publications (numbers depicted). United States and Australia dominates in exploring the effect of leisure-time physical activity on mental health.</p>
Full article ">Figure 4
<p>Pie chart shows the publication trends in different disciplines.</p>
Full article ">Figure 5
<p>Top 50 key phrases identified in the included studies.</p>
Full article ">Figure 6
<p>Co-occurrences of the keywords and the strength of interconnections.</p>
Full article ">Figure 7
<p>Highly cited authors and the connections [<a href="#B16-healthcare-13-00575" class="html-bibr">16</a>,<a href="#B17-healthcare-13-00575" class="html-bibr">17</a>,<a href="#B18-healthcare-13-00575" class="html-bibr">18</a>,<a href="#B19-healthcare-13-00575" class="html-bibr">19</a>,<a href="#B20-healthcare-13-00575" class="html-bibr">20</a>,<a href="#B21-healthcare-13-00575" class="html-bibr">21</a>].</p>
Full article ">Figure 8
<p>Affiliations of the most influential documents.</p>
Full article ">
28 pages, 9250 KiB  
Article
Multi-Hazards and Existing Data: A Transboundary Assessment for Climate Planning
by Alessandra Longo, Chiara Semenzin and Linda Zardo
Land 2025, 14(3), 548; https://doi.org/10.3390/land14030548 - 5 Mar 2025
Viewed by 196
Abstract
Many regions worldwide are exposed to multiple omnipresent hazards occurring in complex interactions. However, multi-hazard assessments are not yet fully integrated into current planning tools, particularly when referring to transboundary areas. This work aims to enable spatial planners to include multi-hazard assessments in [...] Read more.
Many regions worldwide are exposed to multiple omnipresent hazards occurring in complex interactions. However, multi-hazard assessments are not yet fully integrated into current planning tools, particularly when referring to transboundary areas. This work aims to enable spatial planners to include multi-hazard assessments in their climate change adaptation measures using available data. We focus on a set of hazards (e.g., extreme heat, drought, landslide) and propose a four-step methodology to (i) harmonise existing data from different databases and scales for multi-hazard assessment and mapping and (ii) to read identified multi-hazard bundles in homogeneous territorial areas. The methodology, whose outputs are replicable in other EU contexts, is applied to the illustrative case of Northeast Italy. The results show a significant difference between hazards with a ‘dichotomous’ spatial behaviour (shocks) and those with a more complex and nuanced one (stresses). The harmonised maps for the single hazards represent a new piece of knowledge for our territory since, to date, there are no comparable maps with this level of definition to understand hazards’ spatial distribution and interactions between transboundary areas. This study does present some limitations, including putting together data with a remarkable difference in definition for some hazards. Full article
Show Figures

Figure 1

Figure 1
<p>(<b>top</b>) Map and localisation of case study area. (<b>bottom</b>) Focus on key areas of interest outlined and main statistics (surface and population).</p>
Full article ">Figure 2
<p>Workflow illustrating four-step methodology.</p>
Full article ">Figure 3
<p>Relevant hazards according to IPCC and EEA. Hazards and indices selected in this work are highlighted in yellow.</p>
Full article ">Figure 4
<p>Mapping of nine hazards in Triveneto study area according to harmonised classification.</p>
Full article ">Figure 5
<p>Quantification of percentage of land occupied by each hazard out of total extent of study area, according to hazard level, i.e., 0—null to 5—very high.</p>
Full article ">Figure 6
<p>Proposed spatialisation of homogeneous territorial areas for Triveneto study area.</p>
Full article ">Figure 7
<p>Multi-hazard matrix by homogeneous territorial area. Graphs show percentage of land occupied by each hazard in the different areas, according to hazard levels from medium to very high.</p>
Full article ">Figure 8
<p>Overlapping hazards. Map shows average of each selected climatic hazard correlated to homogeneous territorial areas.</p>
Full article ">
17 pages, 1643 KiB  
Article
An Innovative Algorithm for Damage Mapping in Multiaxial Fatigue Using the Stress Scale Factor (SSF) Concept
by Francisco Bumba, Vitor Anes and Luis Reis
Metals 2025, 15(3), 281; https://doi.org/10.3390/met15030281 - 5 Mar 2025
Viewed by 137
Abstract
Predicting damage to materials under multiaxial fatigue is a complex challenge, especially when normal and shear stresses interact in dynamic and non-linear ways. Traditional methods often oversimplify these interactions, leading to less reliable fatigue predictions and limiting their usefulness in real-world applications. To [...] Read more.
Predicting damage to materials under multiaxial fatigue is a complex challenge, especially when normal and shear stresses interact in dynamic and non-linear ways. Traditional methods often oversimplify these interactions, leading to less reliable fatigue predictions and limiting their usefulness in real-world applications. To address this, we present a novel algorithm based on the principles of the Stress Scale Factor (SSF), designed to dynamically evaluate the relative contributions of normal and shear stresses to fatigue damage. By providing a more accurate mapping of multiaxial fatigue damage, this approach enables improved predictions of fatigue life. The methodology combines experimental insights with mathematical modeling to create a flexible and adaptive framework. By making it possible to map multiaxial fatigue damage with greater precision, this SSF-based approach not only enhances the understanding of fatigue behavior but also enables better design decisions. The result is safer, more reliable, and efficient structures across a range of applications. This study bridges the gap between theoretical methods and practical needs, offering engineers and researchers a powerful tool to improve fatigue analysis and optimize structural performance. Full article
Show Figures

Figure 1

Figure 1
<p>Correlation between normal stress amplitude and loading path: (<b>a</b>) pure tensile loading, (<b>b</b>) proportional loading with SAR = 30°, (<b>c</b>) proportional loading with SAR = 45°, and (<b>d</b>) proportional loading with SAR = 60°.</p>
Full article ">Figure 2
<p>Regression analysis of the polynomial constants from <a href="#metals-15-00281-t005" class="html-table">Table 5</a>: (<b>a</b>) third-degree polynomial regression for parameter a, (<b>b</b>) third-degree polynomial regression for parameter b.</p>
Full article ">Figure 3
<p>Regression analysis of the polynomial constant a: (<b>a</b>) two-degree polynomial regression, (<b>b</b>) third-degree polynomial regression.</p>
Full article ">Figure 4
<p>Regression analysis of the polynomial constant b: (<b>a</b>) two-degree polynomial regression, (<b>b</b>) third-degree polynomial regression.</p>
Full article ">
13 pages, 2575 KiB  
Article
Mapping of a Quantitative Trait Locus for Stay-Green Trait in Common Wheat
by Xin Li, Xin Bai, Lijuan Wu, Congya Wang, Xinghui Liu, Qiqi Li, Xiaojun Zhang, Fang Chen, Chengda Lu, Wei Gao and Tianling Cheng
Plants 2025, 14(5), 727; https://doi.org/10.3390/plants14050727 - 27 Feb 2025
Viewed by 226
Abstract
The stay-green (SG) trait enhances photosynthetic activity during the late grain-filling period, benefiting grain yield under drought and heat stresses. CH7034 is a wheat breeding line with SG. To clarify the SG loci carried by CH7034 and obtain linked molecular markers, in this [...] Read more.
The stay-green (SG) trait enhances photosynthetic activity during the late grain-filling period, benefiting grain yield under drought and heat stresses. CH7034 is a wheat breeding line with SG. To clarify the SG loci carried by CH7034 and obtain linked molecular markers, in this study, a recombinant inbred line (RIL) population derived from the cross between CH7034 and non-SG SY95-71 was genotyped using the Wheat17K single-nucleotide polymorphism (SNP) array, and a high-density genetic map covering 21 chromosomes and consisting of 2159 SNP markers was constructed. Then, the chlorophyll content of flag leaf from each RIL was estimated for mapping, and one QTL for SG on chromosome 7D was identified, temporarily named QSg.sxau-7D, with the maximum phenotypic variance explained of 8.81~11.46%. A PCR-based diagnostic marker 7D-16 for QSg.sxau-7D was developed, and the CH7034 allele of 7D-16 corresponded to the higher flag leaf chlorophyll content, while the 7D-16 SY95-71 allele corresponded to the lower value, which confirmed the genetic effect on SG of QSg.sxau-7D. QSg.sxau-7D located in the 526.4~556.2 Mbp interval is different from all the known SG loci on chromosome 7D, and 69 high-confidence annotated genes within the interval expressed throughout the entire period of flag leaf senescence. Moreover, results of an association analysis based on the diagnostic marker showed that there is a positive correlation between QSg.sxau-7D and thousand-grain weight. Our results revealed a novel QTL QSg.sxau-7D whose CH7034 allele had a strong effect on SG, which can be applied in further wheat molecular breeding. Full article
(This article belongs to the Special Issue QTL Mapping of Seed Quality Traits in Crops, 2nd Edition)
Show Figures

Figure 1

Figure 1
<p>Variation in stay green in CH × SY RIL population. (<b>a</b>) Stay-green line. (<b>b</b>) Non-stay-green line. (<b>c</b>) Flag leaf chlorophyll content of RILs. CH: CH7034; SY: SY95-71; SG: stay green; BLUE: best linear unbiased estimation.</p>
Full article ">Figure 2
<p>SNPs from the 17K SNP chip screened to form a genetic map for the RILs. (<b>a</b>) Distribution of SNPs on wheat chromosomes. (<b>b</b>) The number of SNPs on each chromosome.</p>
Full article ">Figure 3
<p>Map position and linked markers of <span class="html-italic">QSg.sxau-7D</span>. (<b>a</b>) Genetic map. (<b>b</b>) Genomic map. (<b>c</b>) Re-mapping result of <span class="html-italic">QSg.sxau-7D</span> integrated with six developed SSR markers. Red boxes represent <span class="html-italic">QSg.sxau-7D</span> region; the linked SNP markers are marked in red, while the developed SSR markers are marked in blue.</p>
Full article ">Figure 4
<p>Expression patterns of 280 annotated genes within <span class="html-italic">QSg.sxau-7D</span> region in wheat flag leaf from the main tiller that harvested at 3, 7, 10, 13, 15, 17, 19, 21, 23, and 26 days after anthesis (DAA). Unexpressed genes are represented by gray squares. From gray to red, the TPM value goes from low to high.</p>
Full article ">Figure 5
<p>Significant differences analysis in genotypes of the diagnostic marker <span class="html-italic">7D-16</span> of <span class="html-italic">QSg.sxau-7D</span> in CH × SY RIL population. * indicates <span class="html-italic">p</span> &lt; 0.05, *** indicates <span class="html-italic">p</span> &lt; 0.001, and **** indicates <span class="html-italic">p</span> &lt; 0.0001, by the <span class="html-italic">t</span>-test.</p>
Full article ">Figure 6
<p>The physical positions of <span class="html-italic">QSg.sxau-7D</span> and the previously reported SG-associated loci on chromosome 7D. The line with rhombic dots indicates QTL interval flanked by markers, and the single rhombic dot indicates the solitary linked marker of QTL. QTLs for flag leaf chlorophyll content that were measured by SPAD value are marked in blue, and the <span class="html-italic">QSg.sxau-7D</span> in this study is marked in red.</p>
Full article ">
18 pages, 3898 KiB  
Article
Use of Real-Time Online Respirometry to Assess Temperature-Induced Metabolic Disorder in Koi Carp (Cyprinus carpio)
by Yi Zhang and Zongming Ren
Water 2025, 17(5), 666; https://doi.org/10.3390/w17050666 - 25 Feb 2025
Viewed by 182
Abstract
This study involved the use of a real-time online respiratory metabolism-monitoring system to examine the effects of water temperature on koi carp metabolism, focusing on the oxygen-consumption rate (OCR), carbon dioxide-excretion rate (CER), and respiratory quotient (RQ). Experiments were conducted at four temperatures: [...] Read more.
This study involved the use of a real-time online respiratory metabolism-monitoring system to examine the effects of water temperature on koi carp metabolism, focusing on the oxygen-consumption rate (OCR), carbon dioxide-excretion rate (CER), and respiratory quotient (RQ). Experiments were conducted at four temperatures: 18 °C, 22 °C, 26 °C, and 30 °C. The results showed that as the temperature increased from 18 °C to 26 °C, the OCR and CER rose significantly, indicating higher metabolic rates. At 30 °C, these indicators declined, reflecting physiological stress and reduced efficiency. The RQ showed minimal fluctuations at 22 °C, suggesting optimal metabolic stability, while at 26 °C and 30 °C, RQ fluctuations increased and rhythmicity was lost, indicating disrupted metabolic activity. Autocorrelation and self-organizing map (SOM) analyses revealed stable circadian rhythms at 18 °C and 22 °C, which were significantly disrupted at higher temperatures. These findings indicate that the optimal temperature range for koi carp is 22 °C to 26 °C, at which temperatures metabolic activity is efficient and rhythms are stable. Beyond this range, metabolism becomes disrupted. This study underscores the importance of maintaining suitable water temperatures in aquaculture to promote fish health and productivity, particularly in the context of climate change. Full article
Show Figures

Figure 1

Figure 1
<p>The online respiratory metabolism-monitoring system (ORMMS). (<b>a</b>), the blue lines represent the power and signal connections, the black solid lines represent the water flow during the circulation phase, and the black dotted lines represent the water flow during the flush phase. (<b>b</b>), the blue solid lines indicate the route of water flow, and the purple solid lines indicate the route of gas flow. Arrows indicate the direction of fluid flow: red arrows indicate the flow in flush mode; blue arrows indicate the flow in circulation mode; and purple arrows indicate the direction of gas flow. Abbreviations: O<sub>2</sub>—oxygen; CO<sub>2</sub>—carbon dioxide; SV—solenoid valve.</p>
Full article ">Figure 2
<p>Real-time oxygen-consumption rate (OCR) of koi over 48 h: solid line (real-time OCR), dotted line with shading (standard deviation), vertical shadow (studied dark period), bar graphs (average OCR for entire study and for light and dark periods). Statistical significance (<span class="html-italic">p</span> &lt; 0.05; ANOVA, Duncan’s multiple range test) is indicated by letters above bars.</p>
Full article ">Figure 3
<p>Real-time carbon dioxide-excretion rate (CER) of koi over 48 h: solid line (real-time CER), dotted line with shading (standard deviation), vertical shadow (studied dark period), bar graphs (average CER for entire study and for light and dark periods). Statistical significance (<span class="html-italic">p</span> &lt; 0.05; ANOVA, Duncan’s multiple range test) is indicated by letters above bars.</p>
Full article ">Figure 4
<p>Real-time respiratory quotient (RQ) of koi over 48 h: solid line (real-time RQ), dotted line with shading (standard deviation), vertical shadow (studied dark period), bar graphs (average RQ for entire study and for light and dark periods). Statistical significance (<span class="html-italic">p</span> &lt; 0.05; ANOVA, Duncan’s multiple range test) is indicated by letters above bars.</p>
Full article ">Figure 5
<p>The columns, from left to right, show the autocorrelation analyses of OCR, CER, and RQ at temperatures of 18 °C, 22 °C, 26 °C, and 30 °C, respectively.</p>
Full article ">Figure 6
<p>Respiratory metabolism of koi, as determined using self-organizing map (SOM) analysis. (<b>a</b>): Ordination map; the red elliptical shadow represents the photoperiod. (<b>b</b>): Cluster map; five clusters classified in the SOM. (<b>c</b>): Ward’s linkage dendrogram. (<b>d</b>): SOM patterns; profiles of OCR, CER, and RQ visualized on the SOM in different treatments. The standing color gradient bar represents levels of respiratory metabolism in the SOM patterns.</p>
Full article ">
19 pages, 2641 KiB  
Article
Nitrogen Fertilization Coupled with Zinc Foliar Applications Modulate the Production, Quality, and Stress Response of Sideritis cypria Plants Grown Hydroponically Under Excess Copper Concentrations
by Nikolaos Tzortzakis, Giannis Neofytou and Antonios Chrysargyris
Plants 2025, 14(5), 691; https://doi.org/10.3390/plants14050691 - 24 Feb 2025
Viewed by 177
Abstract
The demand for medicinal and aromatic plants (MAPs) has grown significantly in recent years, due to their therapeutic value. Among these, Sideritis cypria Post is a promising yet under-evaluated species. Existing research assessing the effects of nitrogen (N) fertilization, zinc (Zn) foliar applications, [...] Read more.
The demand for medicinal and aromatic plants (MAPs) has grown significantly in recent years, due to their therapeutic value. Among these, Sideritis cypria Post is a promising yet under-evaluated species. Existing research assessing the effects of nitrogen (N) fertilization, zinc (Zn) foliar applications, and toxic copper (Cu) concentrations often overlooks MAPs such as S. cypria. Additionally, the interactions among these parameters, as well as their combined roles in MAPs plant physiology and secondary metabolite biosynthesis, have yet to be fully elucidated. In this study, hydroponically grown S. cypria plants were cultivated using nutrient solutions (NSs) with different N (75, 150, and 300 mg L−1) and Cu (5 and 100 μM) levels, combined with foliar spraying (0 and 1.74 mM Zn), to evaluate the growth, mineral uptake, secondary metabolites production and stress response. N levels at 75 and 150 mg L−1 resulted in increased dry matter content, whereas fresh biomass production was preserved. Foliar Zn applications enhanced chlorophylls and antioxidants, contingent upon N and Cu in the NS. Increased N accumulation was observed via the increase in N in the NS, while foliar Zn enhanced its uptake at moderate N levels. Excess Cu stimulated its accumulation, while a reduction was observed with foliar Zn at low and high N levels. Excess Cu increased lipid peroxidation (MDA) at low and moderate N in the NS, while foliar Zn decreased both MDA and hydrogen peroxide, contingent upon Cu and N levels. Low-to-moderate N in the NS can be applied under excess Cu without compromising the yield, quality, and safety of S. cypria plants, while foliar Zn can modulate the stress response of plants under excess Cu and the production of secondary metabolites. These results may be utilized for optimizing nutrient management strategies for the cultivation of MAPs, contributing to conservation efforts by supporting the cultivation of endemic species like S. cypria, considering the potential benefits of Zn foliar applications under Cu-contaminated conditions. Full article
(This article belongs to the Special Issue Responses of Crops to Abiotic Stress)
Show Figures

Figure 1

Figure 1
<p>The effect of N levels (N75, 75 mg L<sup>−1</sup>; N150, 150 mg L<sup>−1</sup>; and N300, 300 mg L<sup>−1</sup>), Zn foliar application (0 and 1.74 mM Zn), and Cu application (no additional, 5 μM Cu; and with additional Cu, 100 μM Cu) on the fresh weight (FW; g) (<b>A</b>) and dry matter (DM; %) (<b>B</b>) of <span class="html-italic">Sideritis cypria</span> plants grown in soilless cultivation. Significant differences (<span class="html-italic">p</span> &lt; 0.05) among the different applications are indicated by different letters. ns: not significant.</p>
Full article ">Figure 2
<p>The effect of N levels (N75, 75 mg L<sup>−1</sup>; N150, 150 mg L<sup>−1</sup>; and N300, 300 mg L<sup>−1</sup>), Zn foliar application (0 and 1.74 mM Zn), and Cu application (no additional, 5 μM Cu; and with additional Cu, 100 μM Cu) on leaf SPAD (<b>A</b>), chlorophyll fluorescence (Fv Fm<sup>−1</sup>) (<b>B</b>), chlorophyll a (Chl a; mg g<sup>−1</sup>) (<b>C</b>), chlorophyll b (Chl b; mg g<sup>−1</sup>) (<b>D</b>), total chlorophylls (Total Chl; mg g<sup>−1</sup>) (<b>E</b>), and total carotenoids (Total Car; mg g<sup>−1</sup>) (<b>F</b>) of <span class="html-italic">Sideritis cypria</span> plants grown in soilless cultivation. Significant differences (<span class="html-italic">p</span> &lt; 0.05) among the different applications are indicated by different letters.</p>
Full article ">Figure 3
<p>The effect of N levels (N75, 75 mg L<sup>−1</sup>; N150, 150 mg L<sup>−1</sup>; and N300, 300 mg L<sup>−1</sup>), Zn foliar application (no foliar, 0 mM Zn; and foliar Zn, 1.74 mM Zn), and Cu application (no additional, 5 μM Cu; and with additional Cu, 100 μM Cu) on leaf and root N (<b>A1</b>,<b>A2</b>), P (<b>B1</b>,<b>B2</b>), K (<b>C1</b>,<b>C2</b>), Na (<b>D1</b>,<b>D2</b>), Fe (<b>E1</b>,<b>E2</b>), Cu (<b>F1</b>,<b>F2</b>), and Zn (<b>G1</b>,<b>G2</b>), respectively, of <span class="html-italic">Sideritis cypria</span> plants grown in soilless cultivation. Significant differences (<span class="html-italic">p</span> &lt; 0.05) among the different applications are indicated by different letters. ns: not significant.</p>
Full article ">Figure 3 Cont.
<p>The effect of N levels (N75, 75 mg L<sup>−1</sup>; N150, 150 mg L<sup>−1</sup>; and N300, 300 mg L<sup>−1</sup>), Zn foliar application (no foliar, 0 mM Zn; and foliar Zn, 1.74 mM Zn), and Cu application (no additional, 5 μM Cu; and with additional Cu, 100 μM Cu) on leaf and root N (<b>A1</b>,<b>A2</b>), P (<b>B1</b>,<b>B2</b>), K (<b>C1</b>,<b>C2</b>), Na (<b>D1</b>,<b>D2</b>), Fe (<b>E1</b>,<b>E2</b>), Cu (<b>F1</b>,<b>F2</b>), and Zn (<b>G1</b>,<b>G2</b>), respectively, of <span class="html-italic">Sideritis cypria</span> plants grown in soilless cultivation. Significant differences (<span class="html-italic">p</span> &lt; 0.05) among the different applications are indicated by different letters. ns: not significant.</p>
Full article ">Figure 4
<p>The effect of N levels (N75, 75 mg L<sup>−1</sup>; N150, 150 mg L<sup>−1</sup>; and N300, 300 mg L<sup>−1</sup>), Zn foliar application (no foliar, 0 mM Zn; and foliar Zn, 1.74 mM Zn), and Cu application (no additional, 5 μM Cu; and with additional Cu, 100 μM Cu) on phenols (<b>A</b>), DPPH (<b>B</b>), FRAP (<b>C</b>), ABTS (<b>D</b>), flavonoids (<b>E</b>), H<sub>2</sub>O<sub>2</sub> (<b>F</b>), and MDA (<b>G</b>) of <span class="html-italic">Sideritis cypria</span> plants grown in soilless cultivation. Significant differences (<span class="html-italic">p</span> &lt; 0.05) among the different applications are indicated by different letters.</p>
Full article ">
22 pages, 12070 KiB  
Article
Nonlinear Viscoelasticity of and Structural Modulation in Guar Gum-Enhanced Triple-Network Hydrogels
by Yi Luo, Werner Pauer and Gerrit A. Luinstra
Polymers 2025, 17(5), 597; https://doi.org/10.3390/polym17050597 - 24 Feb 2025
Viewed by 298
Abstract
The effect of the presence of guar gum (0–0.75 wt%) in a thermo-responsive triple-network (TN) PVA/TA/PVA-MA-g-PNIPAAm hydrogel (PVA: polyvinyl alcohol; MA: methacrylate, PNIPAAm: poly-N-isopropyl acryl amide; TA: tannic acid) with respect to the structural, mechanical, and viscoelastic properties was mapped. A comprehensive analysis, [...] Read more.
The effect of the presence of guar gum (0–0.75 wt%) in a thermo-responsive triple-network (TN) PVA/TA/PVA-MA-g-PNIPAAm hydrogel (PVA: polyvinyl alcohol; MA: methacrylate, PNIPAAm: poly-N-isopropyl acryl amide; TA: tannic acid) with respect to the structural, mechanical, and viscoelastic properties was mapped. A comprehensive analysis, using large-amplitude oscillatory shear (LAOS), SEM imaging, XRD, and mechanical analysis revealed that guar enhances hydrogel crystallinity (up to 30% at 0.75 wt%), which goes along with a strain hardening. The hydrogel achieved superior mechanical performance at a gum concentration of 0.5 wt% with a 40% increase in shear-thickening, an enhanced strain tolerance in nonlinear regimes, and a good mechanical robustness (maximum elongation to break of 500% and stress of 620 kPa). The hydrogel with 0.5 wt% guar exhibited also a good thermal response (equilibrium swelling ratio changed from 8.4 at 5 °C to 2.5 at 50 °C) and an excellent thermal cycling dimensional stability. Higher guar concentrations reduce structural resilience, leading to brittle hydrogels with lower extensibility and viscoelastic stability. Full article
(This article belongs to the Special Issue Mechanic Properties of Polymer Materials)
Show Figures

Figure 1

Figure 1
<p>SEM images of the hydrogels with guar gum (magnifications of 1.00, 5.50, and 15.00 K×).</p>
Full article ">Figure 2
<p>Porosity (Φ) of hydrogels with different contents of guar, calculated as VV/VT, where VV is the volume of void-space (such as fluids) and VT is the total or bulk volume of material.</p>
Full article ">Figure 3
<p>Fracture tensile curves of the guar hydrogels before (<b>a</b>) and after crystallization (<b>b</b>) in an F–T operation.</p>
Full article ">Figure 4
<p>Storage modulus G′(γ<sub>0</sub>) and loss modulus G″(γ<sub>0</sub>) across different concentrations of guar hydrogels.</p>
Full article ">Figure 5
<p>(<b>a</b>) Fourier-Transform rheology spectrum, displaying relative intensity (I<sub>n/1</sub>) versus normalized harmonic frequency (ω/ω<sub>1</sub>) for hydrogel with 0.5 wt% of guar, under an excitation angular frequency of 1 rad/s at 1000% amplitude and (<b>b</b>) relative intensity of the third harmonic (I<sub>3/1</sub>) and the slopes at MAOS.</p>
Full article ">Figure 6
<p>(<b>a</b>) Nonlinear elastic moduli (G′<sub>L</sub> and G′<sub>M</sub>) and (<b>b</b>) dynamic viscosities (η′L and η′M) for a hydrogel comprising 0.5 wt% of guar at ω = 1 rad/s and γ<sub>0</sub> = 1000%, T = 25 °C. Dashed lines denote the associated linear (first harmonic) material properties <math display="inline"><semantics> <mrow> <msubsup> <mi mathvariant="normal">G</mi> <mn>1</mn> <mo>′</mo> </msubsup> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <msubsup> <mi mathvariant="normal">η</mi> <mn>1</mn> <mo>′</mo> </msubsup> </mrow> </semantics></math>.</p>
Full article ">Figure 7
<p>(<b>a</b>) Elastic Lissajous–Bowditch curves for hydrogel containing 0.5 wt% guar at 25 °C yielding the (ω, γ<sub>0</sub>)-Pipkin space, with normalized total stress σ(t)/σ<sub>max</sub> (in black) and normalized elastic stress σ′(t)/σ<sub>max</sub> (in red) relative to the normalized strain γ(t)/γ<sub>0</sub>; (<b>b</b>) corresponding viscous Lissajous–Bowditch curves with normalized total stress σ(t)/σ<sub>max</sub> (in black) and normalized viscous stress σ′(t)/σ<sub>max</sub> (in red) plotted against the normalized strain rate <math display="inline"><semantics> <mrow> <mrow> <mover> <mi mathvariant="normal">γ</mi> <mo>˙</mo> </mover> </mrow> <mfenced> <mi mathvariant="normal">t</mi> </mfenced> <mo>/</mo> <msub> <mrow> <mover> <mi mathvariant="normal">γ</mi> <mo>˙</mo> </mover> </mrow> <mn>0</mn> </msub> </mrow> </semantics></math>.</p>
Full article ">Figure 8
<p>(<b>a</b>) Elastic Lissajous–Bowditch curves: (<b>a</b>) (the total stress σ(t)and the elastic stress σ′(t); viscous Lissajous–Bowditch curves: (<b>b</b>) (the total stress σ(t) and the viscous stress σ″(t) at a constant strain γ<sub>0</sub> of 40%. Elastic Lissajous–Bowditch curves: (<b>c</b>) (the total stress σ(t) and the elastic stress σ′(t); viscous Lissajous–Bowditch curves: (<b>d</b>) (the total stress σ(t)and the viscous stress σ″(t) as function of the strain γ(t)) at a constant angular frequency ω of 1 rad/s.</p>
Full article ">Figure 9
<p>(<b>a</b>) Elastic Lissajous–Bowditch plots illustrating normalized total stress σ(t)/σ<sub>max</sub> (black lines) and normalized elastic stress σ′(t)/σ<sub>max</sub> (red lines) relative to normalized strain γ(t)/γ and (<b>b</b>) viscous Lissajous–Bowditch graphs displaying normalized total stress σ(t)/σ<sub>max</sub> (black lines) and normalized viscous stress σ′(t)/σ<sub>max</sub> (red lines) as functions of normalized strain rate <math display="inline"><semantics> <mrow> <mrow> <mover> <mi mathvariant="normal">γ</mi> <mo>˙</mo> </mover> </mrow> <mfenced> <mi mathvariant="normal">t</mi> </mfenced> <mo>/</mo> <msub> <mrow> <mover> <mi mathvariant="normal">γ</mi> <mo>˙</mo> </mover> </mrow> <mn>0</mn> </msub> </mrow> </semantics></math> across varying concentrations of guar (0 to 0.75 wt%) at ω of 1 rad/s, T = 25 °C.</p>
Full article ">Figure 10
<p>(<b>a</b>) Strain-stiffening ratio S (defined as (G′<sub>L</sub> − G′<sub>M</sub>)/G′<sub>L</sub>) against strain amplitude γ<sub>0</sub> and (<b>b</b>) shear-thickening ratio T (calculated as (η′L − η′M)/η′L) as functions of strain amplitude γ<sub>0</sub> for guar hydrogels (ω = 1 rad/s and T = 25 °C) (C.f. <a href="#app1-polymers-17-00597" class="html-app">Figure S6</a>).</p>
Full article ">Figure 11
<p>Alternating step strain sweep conducted over 100 s, cycling between 1% and 250% strain at ambient temperature with a frequency of 1 Hz on hydrogels with (<b>a</b>) 0.5 wt% and (<b>b</b>) 0 wt% of guar [<a href="#B15-polymers-17-00597" class="html-bibr">15</a>].</p>
Full article ">Figure 12
<p>Equilibrium swelling ratio (ESR) with temperature for the guar-based hydrogels and the picture of 0.5 wt% guar hydrogel showing swelling and deswelling status.</p>
Full article ">Figure 13
<p>Dynamic swelling degree normalized by length (Q<sub>L</sub>) for the hydrogel with 0.5 wt% of guar under cyclic temperature alternation between 40 °C and ambient conditions (grey shading) in deionized water.</p>
Full article ">Figure 14
<p>Measurements of length (L), ultimate length alteration (L<sub>C</sub>), and the corresponding linear rate constant in %/min (R<sub>LC</sub>) for guar hydrogel in deionized water during cycling of 30 min intervals between 40 °C (<b>a</b>) and 20 °C (<b>b</b>).</p>
Full article ">
13 pages, 1473 KiB  
Article
Sensitivity of Lumbar Total Joint Replacement Contact Stresses Under Misalignment Conditions—Finite Element Analysis of a Spine Wear Simulator
by Steven M. Kurtz, Steven A. Rundell, Hannah Spece and Ronald V. Yarbrough
Bioengineering 2025, 12(3), 229; https://doi.org/10.3390/bioengineering12030229 - 24 Feb 2025
Viewed by 336
Abstract
A novel total joint replacement (TJR) that treats lumbar spine degeneration was previously assessed under Mode I and Mode IV conditions. In this study, we relied on these previous wear tests to establish a relationship between finite element model (FEM)-based bearing stresses and [...] Read more.
A novel total joint replacement (TJR) that treats lumbar spine degeneration was previously assessed under Mode I and Mode IV conditions. In this study, we relied on these previous wear tests to establish a relationship between finite element model (FEM)-based bearing stresses and in vitro wear penetration maps. Our modeling effort addressed the following question of interest: Under reasonably worst-case misaligned conditions, do the lumbar total joint replacement (L-TJR) polyethylene stresses and strains remain below values associated with Mode IV impingement wear tests? The FEM was first formally verified and validated using the risk-informed credibility assessment framework established by ASME V&V 40 and FDA guidance. Then, based on criteria for unreasonable misuse outlined in the surgical technique guide, a parametric analysis of reasonably worst-case misalignment using the validated L-TJR FEM was performed. Reasonable misalignment was created by altering device positioning from the baseline condition in three scenarios: Axial Plane Convergence (20–40°), Axial Plane A-P Offset (0–4 mm), and Coronal Plane Tilt (±20°). We found that, for the scenarios considered, the contact pressures, von Mises stresses, and effective strains of the L-TJR-bearing surfaces remained consistent with Mode I (clean) conditions. Specifically, the mechanical response values fell below those determined under Mode IV (worst-case) boundary conditions, which provided the upper-bound benchmarks for the study (peak contact pressure 83.3 MPa, peak von Mises stress 32.2 MPa, and peak effective strain 42%). The L-TJR was judged to be insensitive to axial and coronal misalignment under the in vitro boundary conditions imposed by the study. Full article
(This article belongs to the Section Biomedical Engineering and Biomaterials)
Show Figures

Figure 1

Figure 1
<p>Image depicting the loading conditions of the validated FEM of the L-TJR and in vitro wear simulator. Uniform loading was applied across the superior surface (green surface).</p>
Full article ">Figure 2
<p>Definitions of convergence angle, axial A/P offset, and coronal tilt angle and images of 3D CAD models illustrating the component positioning of cases 1 through 8.</p>
Full article ">Figure 3
<p>Contour plots representing the superposition of all contact pressures over the Mode I duty cycle for the baseline (40°), 30°, and 20° convergence angle simulations. The contact stress plots are viewed on the L-TJR superior polyethylene components from the bottom looking up. The up direction in the figure corresponds to the anterior direction.</p>
Full article ">Figure 4
<p>Contour plots representing the superposition of all contact pressures over the Mode I duty cycle for the baseline (0 mm A-P offset), 2 mm A-P offset, and 4 mm A-P offset simulations. The contact stress plots are viewed on the L-TJR superior polyethylene components from the bottom looking up. The up direction in the figure corresponds to the anterior direction.</p>
Full article ">Figure 5
<p>Contour plots representing the superposition of all contact pressures over the Mode I duty cycle for the baseline, −20°, −10°, 10°, and 20° of coronal tilt simulations. The contact stress plots are viewed on the L-TJR superior polyethylene components from the bottom looking up. The up direction in the figure corresponds to the anterior direction.</p>
Full article ">
16 pages, 6287 KiB  
Article
A Risk Assessment of Water Inrush in Deep Mining in Metal Mines Based on the Coupling Methods of the Analytic Hierarchy Process and Entropy Weight Method: A Case Study of the Huize Lead–Zinc Mine in Northeastern Yunnan, China
by Ronghui Xia, Hongliang Wang, Ticai Hu, Shichong Yuan, Baosheng Huang, Jianguo Wang and Zhouhong Ren
Water 2025, 17(5), 643; https://doi.org/10.3390/w17050643 - 22 Feb 2025
Viewed by 281
Abstract
Deep mining in metal mines faces more and more complex geological conditions, such as “three highs and one disturbance” (high ground stress, high permeability, high temperature, and mining-induced disturbance), which can easily trigger water inrush disasters and seriously affect the safety and efficiency [...] Read more.
Deep mining in metal mines faces more and more complex geological conditions, such as “three highs and one disturbance” (high ground stress, high permeability, high temperature, and mining-induced disturbance), which can easily trigger water inrush disasters and seriously affect the safety and efficiency of deep mining. This paper focuses on the deep hydrogeological structural characteristics of the Huize lead–zinc mine. Firstly, two main factors affecting the production safety of the mining area, namely the water source and water channel of the mine, were analyzed. Based on this analysis, nine factors were determined as indicators for the risk assessment of water inrush, including the water head difference, water-bearing capacity, permeability coefficient, aquifer thickness, water pressure, fault type, fault scale, fault water conductivity, and karst zoning characteristics. Then, a water inrush risk assessment model for the deep mine was constructed, and the weights of the individual factors were determined using the analytic hierarchy process (AHP) and entropy weight method (EWM). Combined with the multi-factor spatial fitting function of the GIS, a zoning map of the risk assessment of water inrush was developed. The results showed that the aquifer groups of the Permian Liangshan Formation and the Carboniferous Maping Formation (P1l + C3m) were relatively safe, whereas the karst fissure aquifer of the Qixia–Maokou Formation (P1q + m) posed a high risk of water inrush, necessitating advanced exploration and water drainage in the area. These findings provide guidance for water control measures in the Huize lead–zinc mine and offer valuable insights into the prediction and prevention of mine water hazards associated with ore body mining in karst aquifers. Full article
(This article belongs to the Section Hydrogeology)
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Location map of the study area. (<b>b</b>) Schematic geological map of study area.</p>
Full article ">Figure 2
<p>Schematic hydrogeological map of study area.</p>
Full article ">Figure 3
<p>Hierarchical structure of evaluation factors.</p>
Full article ">Figure 4
<p>Thematic maps of evaluation factors: (<b>a</b>) water head difference; (<b>b</b>) water-bearing capacity; (<b>c</b>) hydraulic conductivity; (<b>d</b>) aquifer thickness; (<b>e</b>) water pressure; (<b>f</b>) fault type; (<b>g</b>) fault scale; (<b>h</b>) fault water conductivity; (<b>i</b>) karst zoning.</p>
Full article ">Figure 5
<p>Distribution of weight of evaluation factors based on EWM.</p>
Full article ">Figure 6
<p>Zoning map of the risk assessment of water inrush in deep mining.</p>
Full article ">
18 pages, 18199 KiB  
Article
Diel Variation in Summer Stream Temperature in an Idaho Desert Stream and Implications for Identifying Thermal Refuges
by Mel Campbell, Donna Delparte, Matthew Belt, Zhongqi Chen, Christopher C. Caudill and Trevor Caughlin
Climate 2025, 13(3), 44; https://doi.org/10.3390/cli13030044 - 22 Feb 2025
Viewed by 586
Abstract
Thermal refuges in streams are essential for the survival of coldwater fish species such as Redband trout (Oncorhynchus mykiss) in landscapes with stressful or lethal stream temperatures. We utilized an uncrewed aerial system (UAS) mounted with thermal and natural color sensors [...] Read more.
Thermal refuges in streams are essential for the survival of coldwater fish species such as Redband trout (Oncorhynchus mykiss) in landscapes with stressful or lethal stream temperatures. We utilized an uncrewed aerial system (UAS) mounted with thermal and natural color sensors to conduct hourly flights over a 24 h period in the desert stream Little Jacks Creek during late summer when temperatures were near seasonal maximums and streamflow was near seasonal minimums. We used fine-resolution imagery to map stream temperatures and characterize how our thermal sensor exhibits variability across a diel period in an environment where thermal sensor viability had not yet been assessed. Thermal imagery from 3 out of 24 flights showed no significant differences when compared to true water temperatures from in-stream temperature loggers, which appeared to be highly dependent on atmospheric conditions. The thermal imagery (range of 9.17 to 21.04 °C) consistently underestimated HOBO logger stream temperatures (range of 13.6 to 17.1 °C) during cooler, nighttime flights and overestimated temperatures during hotter, afternoon hours, resulting in a global RMSE of 2.12 °C. Between-flight RMSE values ranged from 0.53 °C to 4.00 °C, within the error range of the thermal sensor. The thermal data support existing findings of optimal hours for flying UAS thermal surveys and showed specific patterns in TIR sensor accuracy that were dependent on the time of flight. This study yields valuable lessons for future stream temperature data collection in environments with highly variable temperatures, aiding in the calibration of thermal sensors on UAS missions. Furthermore, our results provide insights into environmental stressors such as increased stream temperatures, which is vital for conservation efforts for organisms that rely on coldwater refuges within desert streams. Full article
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Location of our Little Jacks Creek (LJC) UAS survey (left, red pin) and our RGB orthomosaic of the flight area with temperature logger locations (right). Red markers indicate the northeast, southeast, central, and southwest pools where HOBO loggers were tethered at the surface, middle, and bottom of the water column. (<b>b</b>) Dense vegetation in the horseshoe bend canyon of LJC shown from our takeoff and landing location.</p>
Full article ">Figure 1 Cont.
<p>(<b>a</b>) Location of our Little Jacks Creek (LJC) UAS survey (left, red pin) and our RGB orthomosaic of the flight area with temperature logger locations (right). Red markers indicate the northeast, southeast, central, and southwest pools where HOBO loggers were tethered at the surface, middle, and bottom of the water column. (<b>b</b>) Dense vegetation in the horseshoe bend canyon of LJC shown from our takeoff and landing location.</p>
Full article ">Figure 2
<p>Polystyrene housing for HOBO temperature loggers floating on the surface of LJC (housing cover not pictured).</p>
Full article ">Figure 3
<p>RGB orthomosaic (main) and a zoomed portion (inset) showing one temperature logger housing next to digitized logger point (black triangle).</p>
Full article ">Figure 4
<p>Surface logger temperatures for a full week before and after the survey period (<b>a</b>) (survey period: dashed gray box) and surface logger temperatures for only the survey period (<b>b</b>). The loggers are symbolized by shades of similar colors representing loggers grouped in the same pools.</p>
Full article ">Figure 5
<p>Our RGB orthomosaic overlaid with the Altum TIR band from flights 4, 7, 16, and 23, clipped to the stream boundaries and symbolized with 1<math display="inline"><semantics> <mrow> <mo>°</mo> </mrow> </semantics></math> intervals to highlight potential CWPs. Inset windows show examples of potential CWPs, the spatial shift in the TIR data during the night flight, and “edge effects” from longwave radiation off the cliff faces.</p>
Full article ">Figure 6
<p>Surface and water column temperatures for the (<b>a</b>) southwest, (<b>b</b>) central, (<b>c</b>) southeast, and (<b>d</b>) northeast pools where we tethered the HOBO loggers on the surface, middle, and bottom of the water column.</p>
Full article ">Figure 7
<p>Boxplots of LJC temperatures from the in-stream HOBO loggers and the Altum thermal band at the location of each in-stream logger for all 23 UAS flights, with flight 1 commencing at 13:30 h on September 11 and flight 23 commencing at 12:00 h on September 12. Circles show outliers for both HOBO logger and Altum values.</p>
Full article ">
Back to TopTop