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15 pages, 4774 KiB  
Article
A Feasibility Study on Gradient Boosting Regressor for Subsurface Sensor-Based Surface Instability Assessment
by Shanelle Aira Rodrigazo, Junhwi Cho, Cherry Rose Godes, Yongseong Kim, Yongjin Kim, Seungjoo Lee and Jaeheum Yeon
Land 2025, 14(3), 565; https://doi.org/10.3390/land14030565 - 7 Mar 2025
Abstract
Urban expansion into rural and peri-urban areas increases landslide risks, posing significant threats to infrastructure and public safety. However, most studies focus on surface displacement or meteorological inputs, with less emphasis on subsurface sensor data that could detect early instability precursors. To address [...] Read more.
Urban expansion into rural and peri-urban areas increases landslide risks, posing significant threats to infrastructure and public safety. However, most studies focus on surface displacement or meteorological inputs, with less emphasis on subsurface sensor data that could detect early instability precursors. To address these gaps, this study presents a proof-of-concept validation, establishing the feasibility of using subsurface sensor data to predict near-surface slope displacements. A laboratory-scale slope model (300 cm × 50 cm × 50 cm) at a 30° inclination was subjected to simulated rainfall (150 mm/h for 180 s), with displacement measured at depths of 5 cm and 25 cm using PDP-2000 extensometers. The Gradient Boosting Regressor (GBR) effectively captured the nonlinear relationship between subsurface and surface displacements, achieving high predictive accuracy (R2 = 0.939, MSE = 0.470, MAE = 0.320, RMSE = 0.686). Results demonstrate that, while subsurface sensors do not detect sudden failure events, they effectively capture progressive deformation, offering valuable inputs for multi-sensor EWS in proactive urban planning. Despite demonstrating feasibility, limitations include the controlled laboratory environment and simplified slope conditions. Future work should focus on field-scale validation and multi-sensor fusion to enhance real-world applicability in diverse geological settings. Full article
(This article belongs to the Section Urban Contexts and Urban-Rural Interactions)
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Figure 1

Figure 1
<p>Extensometer setup: (<b>a</b>) example of measurement displacement through extension; (<b>b</b>) angle plate installation; (<b>c</b>) overall extensometer sensor.</p>
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<p>Schematic diagram illustrating the slope model dimensions, extensometer placements, and the positioning of the rainfall simulator for controlled water infiltration.</p>
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<p>Workflow of the laboratory experiment detailing (<b>a</b>) initial slope model setup, (<b>b</b>) controlled rainfall simulation, and (<b>c</b>) post-simulation observations.</p>
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<p>Architecture of GBR.</p>
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<p>Preprocessed sensor reading.</p>
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<p>Comparison of different training ratio metrics.</p>
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<p>CDF of residuals.</p>
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<p>Learning curve of the model (training set size vs. MSE).</p>
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14 pages, 3683 KiB  
Article
Monodisperse Hierarchical N-Doped Carbon Microspheres with Uniform Pores as a Cathode Host for Advanced K–Se Batteries
by Hyun-Jin Kim, Jeong-Ho Na and Seung-Keun Park
Batteries 2025, 11(3), 101; https://doi.org/10.3390/batteries11030101 - 7 Mar 2025
Abstract
K–Se batteries offer high energy density and cost-effectiveness, making them promising candidates for energy storage systems. However, their practical applications are hindered by Se aggregation, sluggish ion diffusion, and significant volumetric expansion. To address these challenges, monodisperse hierarchical N-doped carbon microspheres (NCHS) with [...] Read more.
K–Se batteries offer high energy density and cost-effectiveness, making them promising candidates for energy storage systems. However, their practical applications are hindered by Se aggregation, sluggish ion diffusion, and significant volumetric expansion. To address these challenges, monodisperse hierarchical N-doped carbon microspheres (NCHS) with uniformly sized pores were synthesized as cathode hosts. The flower-like microstructure, formed by the assembly of two-dimensional building blocks, mitigated Se aggregation and facilitated uniform distribution within the pores, enhancing Se utilization. Nitrogen doping, introduced during synthesis, strengthened chemical bonding between selenium and the carbon host, suppressed side reactions, and accelerated reaction kinetics. These synergistic effects enabled efficient ion transport, improved electrolyte accessibility, and enhanced redox reactions. Additionally, the uniform particle and pore sizes of NCHS effectively mitigated volumetric expansion and surface accumulation, ensuring long-term cycling stability and superior electrochemical performance. Se-loaded NCHS (Se@NCHS) exhibited a high discharge capacity of 199.4 mA h g−1 at 0.5 C after 500 cycles with 70.4% capacity retention and achieved 188 mA h g−1 at 3.0 C, outperforming conventional carbon hosts such as Super P. This study highlights the significance of structural and chemical modifications in optimizing cathode materials and offers valuable insights for developing high-performance energy storage systems. Full article
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Graphical abstract

Graphical abstract
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<p>Schematic of Se@NCHS synthesis process.</p>
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<p>Morphology and structure characterizations of NCHS: (<b>a</b>,<b>b</b>) SEM images; (<b>c</b>,<b>d</b>) TEM images; (<b>e</b>–<b>g</b>) HR-TEM image and inlet SAED pattern, and (<b>h</b>) EDX mapping image.</p>
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<p>Morphology and structure characterizations of Se@NCHS: (<b>a</b>,<b>b</b>) SEM images; (<b>c</b>,<b>d</b>) TEM images; (<b>e</b>) HR-TEM image and inlet SAED pattern, and (<b>f</b>) EDX mapping image.</p>
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<p>(<b>a</b>) N<sub>2</sub> adsorption-desorption isotherm curve, (<b>b</b>) HK method differential pore volume plot, (<b>c</b>) BJH pore-size distribution graph of NCHS and Super P, (<b>d</b>) N<sub>2</sub> adsorption-desorption isotherm curve, (<b>e</b>) TGA profiles of Se@NCHS and Se@Super P and (<b>f</b>) the Raman spectra of NCHS, Super P, Se@NCHS and Se@Super P.</p>
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<p>Charge–discharge mechanism of Se@NCHS electrodes; (<b>a</b>) CV curve, (<b>b</b>) charge-discharge 1st profiles at 0.1 C and (<b>c</b>) 1st discharge profile at 0.1 C.</p>
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<p>Electrochemical properties of Se@NCHS and Se@Super P electrodes; (<b>a</b>) Long-term cycle stability and efficiency of charge transfer at 0.5 C current rate and (<b>b</b>) Rate-dependent performance evaluated at varying current densities.</p>
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<p>EIS Nyquist plots of Se@NCHS and Se@Super P electrodes; (<b>a</b>) at fresh cells, (<b>b</b>) after the first cycle, (<b>c</b>) after 100 cycles and (<b>d</b>) Z<sub>re</sub>–w<sup>−1/2</sup> relationship after the 100 cycles.</p>
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<p>GITT analysis of Se@NCHS and Se@Super P electrodes: (<b>a</b>) GITT profiles, the calculated ion diffusion coefficient values (<b>b</b>) during discharging process and (<b>c</b>) during charging process.</p>
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17 pages, 4014 KiB  
Article
Research on SSR Genetic Molecular Markers and Morphological Differences of Different Pelodiscus sinensis Populations
by Yixin Liang, Changqing Huang, Pei Wang, Hewei Xiao, Zi’ao Wang, Jiawei Zeng, Xiaoqing Wang, Shuting Xiong, Yazhou Hu and Qin Qin
Genes 2025, 16(3), 318; https://doi.org/10.3390/genes16030318 - 7 Mar 2025
Abstract
Background/Objectives: The Chinese soft-shelled turtle (Pelodiscus sinensis) is an important species in freshwater aquaculture. Genetic admixture and degradation due to rapid industry expansion threaten sustainable development. This study aims to assess the genetic diversity and structure of six P. sinensis populations [...] Read more.
Background/Objectives: The Chinese soft-shelled turtle (Pelodiscus sinensis) is an important species in freshwater aquaculture. Genetic admixture and degradation due to rapid industry expansion threaten sustainable development. This study aims to assess the genetic diversity and structure of six P. sinensis populations for better management. Methods: We combined morphological analysis and microsatellite markers to evaluate the genetic diversity of six populations. A discriminant function based on morphology was developed, achieving 71.4% classification accuracy. Two SSR markers were identified to specifically distinguish the HS population. Results: The six populations were classified into three subgroups. Frequent gene flow was observed among the CY, W, and DT populations, with most genetic variation occurring within individuals. However, significant genetic differentiation was detected between populations. While gene flow enhanced diversity, it suppressed differentiation. Conclusions: This study provides insights into the genetic structure and diversity of six P. sinensis populations. The discriminant function and SSR markers offer a basis for germplasm conservation and management, supporting sustainable aquaculture development. Full article
(This article belongs to the Special Issue Genetics and Genomics Applied to Aquatic Animal Science—2nd Edition)
16 pages, 5369 KiB  
Article
Genome-Wide Identification and Expression Analysis of Phytosulfokine Peptide Hormone Genes in Camellia sinensis
by Fengshui Yang, Lan Zhang, Qiuying Lu, Qianying Wang, Yanjun Zhou, Qiuhong Wang, Liping Zhang, Kai Shi, Shibei Ge and Xin Li
Int. J. Mol. Sci. 2025, 26(6), 2418; https://doi.org/10.3390/ijms26062418 - 7 Mar 2025
Abstract
Phytosulfokine (PSK) is a tyrosine-sulfated pentapeptide found throughout the plant kingdom, playing key roles in plant growth, development, and responses to biotic and abiotic stresses. However, there is still a lack of a comprehensive analysis of the CsPSK gene family in Camellia sinensis [...] Read more.
Phytosulfokine (PSK) is a tyrosine-sulfated pentapeptide found throughout the plant kingdom, playing key roles in plant growth, development, and responses to biotic and abiotic stresses. However, there is still a lack of a comprehensive analysis of the CsPSK gene family in Camellia sinensis. In this study, we conducted a genome-wide identification and characterized 14 CsPSK genes in tea plants, which are unevenly distributed across seven chromosomes. CsPSK genes encode proteins ranging from 75 to 124 amino acids in length, all belonging to the PSK-α type and containing conserved PSK domains. A synteny analysis revealed that the expansion of the CsPSK gene family is primarily attributed to whole-genome duplication, with homology to Arabidopsis thaliana PSK genes. A promoter region analysis identified cis-regulatory elements related to hormone and stress responses. An expression profile analysis showed that CsPSK genes are highly expressed in roots, stems, flowers, and leaves, and are induced by both biotic and abiotic stresses. Furthermore, an RT-qPCR assay demonstrated that the expression levels of CsPSK8, CsPSK9, and CsPSK10 are significantly upregulated following Discula theae-sinensis infection. These findings establish a basis for further research into the role of the CsPSK gene family in tea plant disease resistance and underlying molecular mechanisms, offering valuable perspectives for developing novel antimicrobial peptides. Full article
(This article belongs to the Special Issue Plants Redox Biology)
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Figure 1

Figure 1
<p>Chromosomal localization of the <span class="html-italic">CsPSK</span> gene family members in tea plants. Chromosome numbers are labeled on the left in organe font color (abbreviated as Chr), while gene positions are indicated on the right in red font color.</p>
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<p>Phylogenetic relationships of the <span class="html-italic">CsPSK</span> gene family in <span class="html-italic">C. sinensis</span> and other plant species. The sequences of PSKs used in this analysis are provided in <a href="#app1-ijms-26-02418" class="html-app">Table S1</a>. Red pentagrams indicate CsPSK proteins. Different clades are highlighted in distinct colors.</p>
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<p>Synteny analysis of <span class="html-italic">CsPSK</span> genes in <span class="html-italic">C. sinensis</span>. Red lines represent duplicated gene pairs, while gray lines indicate syntenic gene pairs in the whole genome.</p>
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<p>Synteny analysis of <span class="html-italic">PSK</span> genes among <span class="html-italic">C. sinensis</span>, <span class="html-italic">A. thaliana, S. lycopersicum</span>. Cs represents the tea plant genome (sky blue), At represents the Arabidopsis genome (soft amber), and Sl represents the tomato genome (deep blue). Gray lines represent syntenic relationships among different genomes and red lines indicate syntenic relationships among the <span class="html-italic">PSK</span> genes.</p>
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<p>The phylogenetic tree, conserved motif, domain and gene structure of the CsPSK proteins. Different motif patterns are indicated by different colored numbered boxes. The blue squares represent the PSK superfamily in the domain pattern. The distribution of untranslated regions (UTRs) and coding sequences (CDSs) of the <span class="html-italic">CsPSK</span> gene family members. The soft green gradient represents UTRs and gradual orange represents CDSs.</p>
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<p>The multiple sequence alignment of the <span class="html-italic">CsPSK</span> gene family. Conserved pentapeptides are indicated by black triangles.</p>
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<p>Analysis of cis-acting elements in the promoter regions of <span class="html-italic">CsPSK</span> genes. The numbers in the grid represent the quantity of cis-acting elements, while the color intensity indicates the abundance of these elements. The right side displays the statistics of cis-acting elements for each gene under four types, including light-responsive elements, hormone-responsive elements, stress-responsive elements, and development-related elements.</p>
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<p>Expression patterns of <span class="html-italic">CsPSK</span> genes under different tissues and stress conditions. (<b>A</b>) Expression patterns of <span class="html-italic">CsPSK</span> genes in eight different tissues of tea plants. Expression responses of tea plants under (<b>B</b>) drought stress, (<b>C</b>) salt stress, (<b>D</b>) leafhopper infestation, and (<b>E</b>) gray blight infection. The size and color of the circles represent high and low expression levels, with red indicating high expression and dark blue indicating low expression.</p>
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<p>The relative expression patterns of <span class="html-italic">CsPSK</span> genes under <span class="html-italic">Discula theae-sinensis</span> infection within 12 h after inoculation. The error bars indicate the standard deviation (SD) based on three biological replicates. Asterisks (*) denote the level of statistical significance, where * indicates <span class="html-italic">p</span> &lt; 0.05, ** indicates <span class="html-italic">p</span> &lt; 0.01), and ns indicates non-significant. Dts, <span class="html-italic">D. theae-sinensis</span>.</p>
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27 pages, 11524 KiB  
Article
GPU Ray Tracing for the Analysis of Light Deflection in Inhomogeneous Refractive Index Fields of Hot Tailored Forming Components
by Pascal Kern, Max Brower-Rabinowitsch, Lennart Hinz, Markus Kästner and Eduard Reithmeier
Sensors 2025, 25(6), 1663; https://doi.org/10.3390/s25061663 - 7 Mar 2025
Abstract
In hot-forming, integrating in situ quality monitoring is essential for the early detection of thermally induced geometric deviations, especially in the production of hybrid bulk metal parts. Although hybrid components are key to meeting modern technical requirements and saving resources, they exhibit complex [...] Read more.
In hot-forming, integrating in situ quality monitoring is essential for the early detection of thermally induced geometric deviations, especially in the production of hybrid bulk metal parts. Although hybrid components are key to meeting modern technical requirements and saving resources, they exhibit complex shrinkage behavior due to differing thermal expansion coefficients. During forming, these components are exposed to considerable temperature gradients, which result in density fluctuations in the ambient air. These fluctuations create an inhomogeneous refractive index field (IRIF), which significantly affects the accuracy of optical geometry reconstruction systems due to light deflection. This study utilizes existing simulation IRIF data to predict the magnitude and orientation of refractive index fluctuations. A light deflection simulation run on a GPU-accelerated ray tracing framework is used to assess the impact of IRIFs on optical measurements. The results of this simulation are used as a basis for selecting optimized measurement positions, reducing and quantifying uncertainties in surface reconstruction, and, therefore, improving the reliability of quality control in hot-forming applications. Full article
(This article belongs to the Section Optical Sensors)
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Figure 1

Figure 1
<p>A camera records a hot measurement object and is influenced by an inhomogeneous refractive index field.</p>
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<p>Visualization of Snell’s law of refraction.</p>
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<p>Visualization of ray tracing through an inhomogeneous refractive medium.</p>
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<p>General procedure for calculating viewing ray deviations.</p>
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<p>Core ray tracing functions.</p>
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<p>Reduction in edge formations using the Taubin filter: (<b>a</b>) the original and (<b>b</b>) with the applied Taubin filter.</p>
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<p>Illustration of the impact of COMSOL configuration on the simulation results. The color-coded viewing ray displacement on the surface of a cylinder during ray tracing through the IRIF is presented. (<b>a</b>) Configuration B+: normal mesh resolution and high isosurface resolution. (<b>b</b>) Configuration D: extra-fine mesh resolution and normal isosurface resolution.</p>
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<p>The number of viewing rays used in ray tracing exhibits a linear relationship with runtime.</p>
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<p>The number of polygons per boundary layer exhibits an approximately linear relationship with runtime.</p>
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<p>The number of boundary layers used exhibits a linear relationship with runtime and a diminishing trend with respect to the quality metric.</p>
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<p>Smoothing the boundary layers has no impact on runtime. The RMSE relative to the reference increases linearly with the number of smoothing iterations.</p>
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<p>Runtime and RMSE values for different simulation-based mesh configurations.</p>
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<p>Resolutions depending on the angle of incidence with (<b>a</b>) resolutions at <math display="inline"><semantics> <mrow> <msub> <mi>θ</mi> <mi>inc</mi> </msub> <mo>=</mo> <mn>0</mn> <mo>°</mo> </mrow> </semantics></math>; (<b>b</b>) describes the resolutions at <math display="inline"><semantics> <mrow> <msub> <mi>θ</mi> <mi>inc</mi> </msub> <mo>=</mo> <mn>45</mn> <mo>°</mo> </mrow> </semantics></math>, and (<b>c</b>) visualizes resolutions for a cylinder.</p>
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<p>Calculation time (<b>a</b>) and measurement object coverage (<b>b</b>) for each camera position.</p>
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<p>(<b>a</b>) Displacements for the surface area of the cylinder head. (<b>b</b>) Displacements for the lateral surface area of the cylinder. (<b>c</b>) Displacements for the total surface area of the cylinder. (<b>d</b>) Angle of incidence.</p>
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<p>Lateral (<b>a</b>) and axial (<b>b</b>) resolutions for each camera position.</p>
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<p>(<b>a</b>) Steel–aluminum hybrid cylinder geometry. (<b>b</b>) Mean displacement for each camera position. (<b>c</b>) Camera position with the highest displacement. (<b>d</b>) Camera position with the lowest displacement.</p>
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<p>(<b>a</b>) Bevel gear geometry. (<b>b</b>) Mean displacement for each camera position. (<b>c</b>) Camera position with the highest displacement. (<b>d</b>) Camera position with the lowest displacement.</p>
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<p>(<b>a</b>) Wishbone geometry. (<b>b</b>) Mean displacement for each camera position. (<b>c</b>) Camera position with the highest displacement. (<b>d</b>) Camera position with the lowest displacement.</p>
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<p>Investigation of a bevel gear tooth based on ray tracing metrics: (<b>a</b>) total mean displacement per camera position; (<b>b</b>) total coverage per camera position; (<b>c</b>) total mean axial resolution per camera position; (<b>d</b>) total mean lateral resolution per camera position; (<b>e</b>) combined metric per camera position; (<b>f</b>) camera position with the lowest displacement value.</p>
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<p>The intersection of boundary layers can lead to ray tracing errors as the boundary layers are sequentially incorporated into the ray tracing process hierarchically.</p>
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<p>Number of polygons (<b>a</b>) and number of ray hits (<b>b</b>) per camera position.</p>
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<p>Distributions of the four metrics for the simulation from <a href="#sensors-25-01663-f020" class="html-fig">Figure 20</a>.</p>
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<p>Normalized distributions of the four metrics for the simulation from <a href="#sensors-25-01663-f020" class="html-fig">Figure 20</a>.</p>
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23 pages, 4703 KiB  
Article
Exploring the Design Space of Low-Thrust Transfers with Ballistic Terminal Coast Segments in Cis-Lunar Space
by Kevin I. Alvarado and Sandeep K. Singh
Aerospace 2025, 12(3), 217; https://doi.org/10.3390/aerospace12030217 - 7 Mar 2025
Abstract
Spacecraft catering to the Lunar Gateway or other “permanent” stations in the lunar vicinity would require frequent travel between periodic orbits around the Earth–Moon L1 and L2 Lagrange points. The transition through the Hill sphere is often characterized by close passages [...] Read more.
Spacecraft catering to the Lunar Gateway or other “permanent” stations in the lunar vicinity would require frequent travel between periodic orbits around the Earth–Moon L1 and L2 Lagrange points. The transition through the Hill sphere is often characterized by close passages of our nearest neighbor—rendering the optimization problem numerically challenging due to the increased local sensitivities. Depending on the mission requirements and resource constraints, transfer architectures must be studied, and trade-offs between flight time and fuel consumption quantified. While direct low-thrust transfers between the circular restricted three-body problem periodic orbit families have been studied, the asymptotic flow in the neighborhood of the periodic orbits could be leveraged for expansion and densification of the solution space. This paper presents an approach to achieve a dense mapping of manifold-assisted, low-thrust transfers based on initial and terminal coast segments. Continuation schemes are utilized to attain the powered intermediate time-optimal segment through a multi-shooting approach. Interesting insights regarding the linear correlation between ΔV and change in reduced two-body osculating elements associated with the initial-terminal conditions are discussed. These insights could inform the subsequent filtering of the osculating selenocentric periapsis map and provide additional interesting and efficient solutions. The described approach is anticipated to be extremely useful for future crewed and robotic cis-lunar operations. Full article
(This article belongs to the Section Astronautics & Space Science)
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Figure 1

Figure 1
<p>Generalized dynamics of the restricted three-body problem.</p>
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<p>Invariant manifolds between <math display="inline"><semantics> <msub> <mi>L</mi> <mn>1</mn> </msub> </semantics></math> and <math display="inline"><semantics> <msub> <mi>L</mi> <mn>2</mn> </msub> </semantics></math> northern halo orbits in the Earth–Moon system with Jacobi constants 3.0326 and 3.1166, respectively.</p>
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<p>(<b>Left</b>) fixed-free single-shooting scheme. (<b>Right</b>) free-free multi-shooting scheme.</p>
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<p>(<b>Left</b>) plane piercing points. (<b>Right</b>) sphere piercing points with radius of <math display="inline"><semantics> <mrow> <mn>15</mn> <msub> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">m</mi> </msub> </mrow> </semantics></math>.</p>
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<p>(<b>Left</b>) unconstrained osculating boundary conditions in the lunar neighborhood. (<b>Right</b>) constrained osculating boundary conditions in the lunar neighborhood.</p>
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<p>Transfer arcs from <math display="inline"><semantics> <msub> <mi>L</mi> <mn>1</mn> </msub> </semantics></math> to <math display="inline"><semantics> <msub> <mi>L</mi> <mn>2</mn> </msub> </semantics></math> periodic orbits with the secondary shown.</p>
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<p>Direct time-optimal trajectories from all initial states to one final state with varying initial thrust accelerations of <math display="inline"><semantics> <mrow> <mn>20</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math>, <math display="inline"><semantics> <mrow> <mn>10</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math>, and <math display="inline"><semantics> <mrow> <mn>5</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math>, from left to right, respectively.</p>
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<p>Pork chop plot for all combinations of TPBVPs for end-to-end <math display="inline"><semantics> <msub> <mi>L</mi> <mn>1</mn> </msub> </semantics></math> to <math display="inline"><semantics> <msub> <mi>L</mi> <mn>2</mn> </msub> </semantics></math> transfers using an initial thrust acceleration of <math display="inline"><semantics> <mrow> <mn>1</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math> along with selected trajectory plots, from left to right, respectively.</p>
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<p>Best time-optimal direct transfer from <math display="inline"><semantics> <msub> <mi>L</mi> <mn>1</mn> </msub> </semantics></math> to <math display="inline"><semantics> <msub> <mi>L</mi> <mn>2</mn> </msub> </semantics></math> using <math display="inline"><semantics> <mrow> <mn>1</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math> thrust acceleration, with the Moon and orbits shown.</p>
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<p>Solution bifurcation for plane-piercing states using <math display="inline"><semantics> <mrow> <mn>5</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math> thrust acceleration with the Moon and manifolds shown (magenta: unstable; green: stable).</p>
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<p>Solution space for different thrust values on the same <math display="inline"><semantics> <mrow> <mn>20</mn> <mo> </mo> <msub> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">m</mi> </msub> </mrow> </semantics></math> target states.</p>
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<p>Solution space for thrust acceleration: <math display="inline"><semantics> <mrow> <mn>1</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>−</mo> <mn>3</mn> </mrow> </msup> </mrow> </semantics></math> m/<math display="inline"><semantics> <msup> <mi mathvariant="normal">s</mi> <mn>2</mn> </msup> </semantics></math> with 18, 14, and 10 <math display="inline"><semantics> <msub> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">m</mi> </msub> </semantics></math>.</p>
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<p>Pork chop plot for 18 <math display="inline"><semantics> <msub> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">m</mi> </msub> </semantics></math> (<b>left</b>) with most fuel-efficient solution shown (<b>right</b>).</p>
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<p>Pork chop plot for 14 <math display="inline"><semantics> <msub> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">m</mi> </msub> </semantics></math> (<b>left</b>) with most fuel-efficient solution shown (<b>right</b>).</p>
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<p>Pork chop plot for 10 <math display="inline"><semantics> <msub> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">m</mi> </msub> </semantics></math> (<b>left</b>) with most fuel-efficient solution shown (<b>right</b>).</p>
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<p>Solutions for the various seleno-centric osculating condition pairs.</p>
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<p>Most fuel-efficient solutions from all devised filtering approaches.</p>
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31 pages, 1042 KiB  
Article
Spatial Effects and Driving Factors of Consumption Upgrades on Municipal Solid Waste Eco-Efficiency, Considering Emission Outputs
by Baihui Jin and Wei Li
Sustainability 2025, 17(6), 2356; https://doi.org/10.3390/su17062356 - 7 Mar 2025
Abstract
To achieve the goal of building zero-waste cities, managing greenhouse gas (GHG) emissions generated from municipal solid waste (MSW) treatment is a critical step toward carbon neutrality. Waste produced by consumption activities constitutes an essential component of MSW management. Using the Super Slacks-Based [...] Read more.
To achieve the goal of building zero-waste cities, managing greenhouse gas (GHG) emissions generated from municipal solid waste (MSW) treatment is a critical step toward carbon neutrality. Waste produced by consumption activities constitutes an essential component of MSW management. Using the Super Slacks-Based Measure Data Envelopment Analysis (SSBM-DEA) model and the Spatial Durbin Model (SDM), this study investigates the spatial impacts of consumption upgrading (CU) on municipal waste management across 30 provinces in China, with a particular focus on GHGs as undesirable outputs. In this study, we construct a framework from the dimensions of consumption level, consumption structure, and green consumption. Additionally, other socioeconomic factors influencing waste management are explored. The results indicate a convergence trend in the uneven distribution of consumption upgrading, with the gaps between regions gradually narrowing. Consumption upgrading significantly enhances the eco-efficiency of local waste management and exhibits notable spatial spillover effects, positively influencing the eco-efficiency of neighboring regions. Furthermore, the promotion effect of consumption upgrading on the central and western regions, compared with the eastern region, is more pronounced. This indicates that the technological catch-up resulting from consumption upgrading, supported by policies, can further enhance the eco-efficiency of MSW. This study also provides insights for other regions transitioning from scale expansion to high-quality development in waste management. Full article
19 pages, 1581 KiB  
Article
A Structural Credit Risk Model with Jumps Based on Uncertainty Theory
by Hong Huang, Meihua Jiang, Yufu Ning and Shuai Wang
Mathematics 2025, 13(6), 897; https://doi.org/10.3390/math13060897 - 7 Mar 2025
Abstract
This study, within the framework of uncertainty theory, employs an uncertain differential equation with jumps to model the asset value process of a company, establishing a structured model of uncertain credit risk that incorporates jumps. This model is applied to the pricing of [...] Read more.
This study, within the framework of uncertainty theory, employs an uncertain differential equation with jumps to model the asset value process of a company, establishing a structured model of uncertain credit risk that incorporates jumps. This model is applied to the pricing of two types of credit derivatives, yielding pricing formulas for corporate zero-coupon bonds and Credit Default Swap (CDS). Through numerical analysis, we examine the impact of asset value volatility and jump magnitude on corporate default uncertainty, as well as the influence of jump magnitude on the pricing of zero-coupon bonds and CDS. The results indicate that an increase in volatility levels significantly enhances default uncertainty, and an expansion in the magnitude of negative jumps not only directly elevates default risk but also leads to a significant increase in the value of zero-coupon bonds and the price of CDS through a risk premium adjustment mechanism. Therefore, when assessing corporate default risk and pricing credit derivatives, the disturbance of asset value jumps must be considered a crucial factor. Full article
(This article belongs to the Special Issue Uncertainty Theory and Applications)
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<p>Pictorial representation of the proposed work.</p>
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<p>The variation in <math display="inline"><semantics> <msub> <mi mathvariant="script">M</mi> <mi>T</mi> </msub> </semantics></math> with respect to <math display="inline"><semantics> <mi>η</mi> </semantics></math>.</p>
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<p>The variation in <math display="inline"><semantics> <msub> <mi mathvariant="script">M</mi> <mi>T</mi> </msub> </semantics></math> with respect to <math display="inline"><semantics> <mi>σ</mi> </semantics></math>.</p>
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<p>The variation in <math display="inline"><semantics> <msub> <mi mathvariant="script">M</mi> <mi>T</mi> </msub> </semantics></math> with respect to <math display="inline"><semantics> <mi>μ</mi> </semantics></math>.</p>
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<p>The research approach of this section.</p>
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<p>The variation in <math display="inline"><semantics> <mrow> <mi>C</mi> <mi>S</mi> <mfenced separators="" open="(" close=")"> <mrow> <mn>0</mn> <mo>,</mo> <mi>T</mi> </mrow> </mfenced> </mrow> </semantics></math> with respect to <math display="inline"><semantics> <mi>η</mi> </semantics></math>.</p>
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<p>The variation in <math display="inline"><semantics> <mi>ω</mi> </semantics></math> with respect to <math display="inline"><semantics> <mi>η</mi> </semantics></math>.</p>
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27 pages, 6155 KiB  
Article
Construction and Zoning of Ecological Security Patterns in Yichang City
by Qi Zhang, Yi Sun, Diwei Tang, Hu Cheng and Yi Tu
Sustainability 2025, 17(6), 2354; https://doi.org/10.3390/su17062354 - 7 Mar 2025
Abstract
The study of ecological security patterns is of great significance to the balance between regional economic development and environmental protection. By optimizing the regional ecological security pattern through reasonable land-use planning and resource management strategies, the purpose of maintaining ecosystem stability and improving [...] Read more.
The study of ecological security patterns is of great significance to the balance between regional economic development and environmental protection. By optimizing the regional ecological security pattern through reasonable land-use planning and resource management strategies, the purpose of maintaining ecosystem stability and improving ecosystem service capacity can be achieved, and ultimately regional ecological security can be achieved. As a typical ecological civilization city in the middle reaches of the Yangtze River, Yichang City is also facing the dual challenges of urban expansion and environmental pressure. The construction and optimization of its ecological security pattern is the key to achieving the harmonious coexistence of economic development and environmental protection and ensuring regional sustainable development. Based on the ecological environment characteristics and land-use data of Yichang City, this paper uses morphological spatial pattern analysis and landscape connectivity analysis to identify core ecological sources, constructs a comprehensive ecological resistance surface based on the sensitivity–pressure–resilience (SPR) model, and combines circuit theory and Linkage Mapper tools to extract ecological corridors, ecological pinch points, and ecological barrier points and construct the ecological security pattern of Yichang City with ecological elements of points, lines, and surfaces. Finally, the community mining method was introduced and combined with habitat quality to analyze the spatial topological structure of the ecological network in Yichang City and conduct ecological security zoning management. The following conclusions were drawn: Yichang City has a good ecological background value. A total of 64 core ecological sources were screened out with a total area of 3239.5 km². In total, 157 ecological corridors in Yichang City were identified. These corridors were divided into 104 general corridors, 42 important corridors, and 11 key corridors according to the flow centrality score. In addition, 49 key ecological pinch points and 36 ecological barrier points were identified. The combination of these points, lines, and surfaces formed the ecological security pattern of Yichang City. Based on the community mining algorithm in complex networks and the principle of Thiessen polygons, Yichang City was divided into five ecological functional zones. Among them, Community No. 2 has the highest ecological security level, high vegetation coverage, close distribution of ecological sources, a large number of corridors, and high connectivity. Community No. 5 has the largest area, but it contains most of the human activity space and construction and development zones, with low habitat quality and severely squeezed ecological space. In this regard, large-scale ecological restoration projects should be implemented, such as artificial wetland construction and ecological island establishment, to supplement ecological activity space and mobility and enhance ecosystem service functions. This study aims to construct a multi-scale ecological security pattern in Yichang City, propose a dynamic zoning management strategy based on complex network analysis, and provide a scientific basis for ecological protection and restoration in rapidly urbanizing areas. Full article
19 pages, 4849 KiB  
Article
Impact of Supercritical Carbon Dioxide on Pore Structure and Gas Transport in Bituminous Coal: An Integrated Experiment and Simulation
by Kui Dong, Zhiyu Niu, Shaoqi Kong and Bingyi Jia
Molecules 2025, 30(6), 1200; https://doi.org/10.3390/molecules30061200 - 7 Mar 2025
Abstract
The injection of CO2 into coal reservoirs occurs in its supercritical state (ScCO2), which significantly alters the pore structure and chemical composition of coal, thereby influencing the adsorption and diffusion behavior of methane (CH4). Understanding these changes is [...] Read more.
The injection of CO2 into coal reservoirs occurs in its supercritical state (ScCO2), which significantly alters the pore structure and chemical composition of coal, thereby influencing the adsorption and diffusion behavior of methane (CH4). Understanding these changes is crucial for optimizing CH4 extraction and improving CO2 sequestration efficiency. This study aims to investigate the effects of ScCO2 on the pore structure, chemical bonds, and CH4 diffusion mechanisms in bituminous coal to provide insights into coal reservoir stimulation and CO2 storage. By utilizing high-pressure CO2 injection adsorption, low-pressure CO2 gas adsorption (LP-CO2-GA), Fourier-transform infrared spectroscopy (FTIR), and reactive force field molecular dynamics (ReaxFF-MD) simulations, this study examines the multi-scale changes in coal at the nano- and molecular levels. The following results were found: Pore Structure Evolution: After ScCO2 treatment, micropore volume increased by 19.1%, and specific surface area increased by 11.2%, while mesopore volume and specific surface area increased by 14.4% and 5.7%, respectively. Chemical Composition Changes: The content of aromatic structures, oxygen-containing functional groups, and hydroxyl groups decreased, while aliphatic structures increased. Specific molecular changes included an increase in (CH2)n, 2H, 1H, and secondary alcohol (-C-OH) and phenol (-C-O) groups, while Car-Car and Car-H bonds decreased. Mechanisms of Pore Volume Changes: The pore structure evolves through three distinct phases: Swelling Phase: Breakage of low-energy bonds generates new micropores. Aromatic structure expansion reduces intramolecular spacing but increases intermolecular spacing, causing a decrease in micropore volume and an increase in mesopore volume. Early Dissolution Phase: Continued bond breakage increases micropore volume, while released aliphatic and aromatic structures partially occupy these pores, converting some mesopores into micropores. Later Dissolution Phase: Minimal chemical bond alterations occur, but weakened π-π interactions and van der Waals forces between aromatic layers result in further mesopore volume expansion. Impact on CH4 Diffusion: Changes in pore volume directly affect CH4 migration. In the early stages of ScCO2 interaction, pore shrinkage reduces the mean square displacement (MSD) and self-diffusion coefficient of CH4. However, as the reaction progresses, pore expansion enhances CH4 diffusion, ultimately improving gas extraction efficiency. This study provides a fundamental understanding of how ScCO2 modifies coal structure and CH4 transport properties, offering theoretical guidance for enhanced CH4 recovery and CO2 sequestration strategies. Full article
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<p>ScCO<sub>2</sub> and TL interaction mechanism analysis flow chart.</p>
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<p>(<b>a</b>) Macromolecular structure of TL; (<b>b</b>) geometric optimization model of TL; (<b>c</b>) supramolecular structure of TL; and (<b>d</b>) ScCO<sub>2</sub> injection model (C: gray; H: white; O: red; S: yellow; N: blue).</p>
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<p>Relationship between the absolute adsorption capacity of TL coal and CO<sub>2</sub> injection pressure.</p>
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<p>FTIR change characteristics before and after ScCO<sub>2</sub> treatment.</p>
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<p>Characteristics of chemical bond changes in TL samples during ScCO<sub>2</sub> treatment.</p>
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<p>The process of new micropore formation during ScCO<sub>2</sub> reactions (C: gray; O: red; N: blue; S: Yellow).</p>
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<p>The process of micropore deformation during ScCO<sub>2</sub> reactions (C: gray; O: red).</p>
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<p>The process of mesopore deformation during ScCO<sub>2</sub> reactions (C: gray; O: red; N: blue).</p>
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<p>Changes in MSD of CH4 during ScCO<sub>2</sub> reaction.</p>
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<p>Self-diffusion coefficients change during the ScCO<sub>2</sub> reaction.</p>
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21 pages, 2734 KiB  
Article
The Chimeric Antigen Receptor T Cell Target Claudin 6 Is a Marker for Early Organ-Specific Epithelial Progenitors and Is Expressed in Some Pediatric Solid Tumor Entities
by Larissa Seidmann, Arthur Wingerter, Marie Oliver Metzig, Angelina Bornas, Khalifa El Malki, Arsenij Ustjanzew, Franziska Ortmüller, Yevgeniy Kamyshanskiy, Thomas Kindler, Mark Laible, Xenia Mohr, Nicole Henninger, Alexandra Russo, Olaf Beck, Francesca Alt, Pia Wehling, Wilfried Roth, Claudia Paret and Jörg Faber
Cancers 2025, 17(6), 920; https://doi.org/10.3390/cancers17060920 - 7 Mar 2025
Abstract
Background/Objectives: The oncofetal membrane protein Claudin 6 (CLDN6) is an attractive target for T cell-based therapies. There is a lack of detailed analyses on the age-dependent expression of CLDN6 in normal tissues is lacking, which limits the expansion of CLDN6 CAR-T cell [...] Read more.
Background/Objectives: The oncofetal membrane protein Claudin 6 (CLDN6) is an attractive target for T cell-based therapies. There is a lack of detailed analyses on the age-dependent expression of CLDN6 in normal tissues is lacking, which limits the expansion of CLDN6 CAR-T cell clinical trials to pediatric populations. Methods: We analyzed CLDN6 expression in extracranial solid tumors and normal tissues of children using RNA-sequencing data from over 500 pediatric solid tumor samples, qRT-PCR and immunohistochemistry (IHC) in more than 100 fresh-frozen tumor samples and, approximately, 250 formalin-fixed paraffin-embedded (FFPE) samples. We examined normal tissue expression via qRT-PCR in 32 different infant tissues and via IHC in roughly 290 tissues from donors across four age groups, as well as in fetal autopsy samples. Results: In fetal tissues, we detected CLDN6 expression primarily in the epithelial cells of several organs, including the skin, lungs, kidneys, intestinal tract, and pancreas, but not in undifferentiated blastemal cells. Postnatally, we found CLDN6-positive epithelial progenitors only during the first few weeks of life. In older-age groups, isolated clusters of CLDN6-positive progenitors were present, but in scarce quantities. In tumor tissues, we found strong and homogeneous CLDN6 expression in desmoplastic small round cell tumors and germ cell tumors. Wilms tumors demonstrated heterogeneous CLDN6 expression, notably absent in the blastemal component. Conclusions: These findings highlight an organ-specific presence of CLDN6-positive epithelial precursors that largely disappear in terminally differentiated epithelia within weeks after birth. Therefore, our data support CLDN6 as a viable therapeutic target in pediatric patients and justify their inclusion in basket studies for anti-CLDN6-based therapies. Full article
(This article belongs to the Special Issue Targeted Therapies for Pediatric Solid Tumors (2nd Edition))
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<p>CLDN6 expression is predicted in solid and blood cancer in the pediatric population. Batch-corrected and transformed gene expression values of CLDN6 across blood cancer (<b>A</b>) and extracranial cancer types (<b>B</b>). The lower half represents a boxplot per tumor type, where the box range from the first to third quantiles, divided by a line indicating the median, and whiskers demonstrate the largest and lowest values no further than 1.5 × IQR from the hinge. The upper half shows the distribution of the samples, where each dot represents a sample. B-ALL = B-cell Acute Lymphoblastic Leukemia, T-ALL = T cell Acute Lymphoblastic Leukemia, AML = Acute Myeloid Leukemia, AMKL = Acute Megakaryoblastic Leukemia, AMML = Acute Myelomonocytic Leukemia, AL = Acute Leukemias, DLBCL = Diffuse Large B-cell Lymphoma, RMS = Rhabdomyosarcoma, DSRCT = Desmoplastic Small Round Cell Tumor.</p>
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<p>CLDN6 mRNA is present in the normal tissues of infants and in pediatric tumors. (<b>A</b>) Distribution of the solid tumor samples analyzed by qRT–PCR. (<b>B</b>) Expression of CLDN6 analyzed by qRT–PCR in normal and tumor tissues. Relative expression is shown as a box and whisker plot; the box range is from minimum to maximum value. Each dot represents a sample. In the normal tissues boxplot, red dots indicate lung, purple dots indicate kidney, bright green dots indicate pancreas, blue dots indicate skin, dark green dots indicate renal pelvis and orange dots indicate colon samples. In the normal kidney boxplot, a purple triangle indicates the medulla and the star cortex samples. In the boxplot for “nephroblastoma,” the brown dots and triangles represent metastases from two different patients, while the yellow triangle indicates the nephroblastoma component of a tumor that also presented with nephroblastomatosis (depicted as a yellow dot in the “other tumor entities” boxplot). Further, in the boxplot “other tumor entities”, a pink dot represents a DSRCT sample. (<b>C</b>) Relative expression of CLDN6 in subtypes of GCT. (<b>D</b>) Relative expression of CLDN6 in subtypes of nephroblastoma.</p>
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<p>Organ–specific presence of CLDN6–positive epithelial precursors (5th week of pregnancy). Tissues were stained with an anti–CLDN6 specific antibody. The evaluation of the staining can be found in <a href="#cancers-17-00920-t004" class="html-table">Table 4</a>. Embryonic epithelium of (<b>A</b>) kidney (score 2+/3+), (<b>B</b>) Intestine (score 3+), (<b>C</b>) liver ducts (score 2+/3+), (<b>D</b>) peritoneum (score 2+). (<b>E</b>) Yolk sac (score 2+/3+). (<b>F</b>) Chorionic epithelium of the placenta (score 2+/3+).</p>
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<p>CLDN6 expression is lost after birth. IHC was performed with the indicated organs and in different age groups, including embryo. The picture frame in red indicates tissues isolated from an embryo at the fifth week of pregnancy, while blue indicates a newborn (1 week old) and green indicates 13- to 18-years-old donors. Expression of CLDN6 in sparse small clusters can be observed in pancreas, skin, kidney and lung after birth. Negative control (embryonic skin, right without frame). The arrows indicate the CLDN6 positive epithelial cells.</p>
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<p>CLDN6 was analyzed by immunohistochemistry in DSRCT ((<b>A</b>), 100% of tumor cells are positive, with score 3+); Yolk sac tumor ((<b>B</b>), 95% of the tumor cells are positive, with score 2+/3+) and high-risk WTs after therapy (<b>C</b>,<b>E</b>,<b>F</b>). Blastema (<b>F</b>), tumor stroma and part of the tumor epithelium (<b>E</b>) were CLDN6-negative, individual tumor cells in the metastasis were positive (<b>C</b>), 5%. The persistent immature nephroblastomatosis foci were partially positive (<b>D</b>). In the graph, the intensity and heterogeneity of CLDN6 expression across pediatric tumor entities is reported. The y-axis indicates the percentage of positive tumor cells (with a score of 2+/3+). Each dot represents a sample. The median value is indicated. Within GCT, the yellow dot indicates a mature teratoma, the green dots yolk sac tumors, the pink dot a dysgerminoma and the black dot a mixed subtype. Within “WT”, the blue dots indicate high-risk patients.</p>
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24 pages, 5803 KiB  
Article
Design, Modeling, and Optimization of a Nearly Constant Displacement Reducer with Completely Distributed Compliance
by Yanchao Tong, Beibei Hou, Shuaishuai Lu, Pengbo Liu, Zhi Yang and Peng Yan
Appl. Sci. 2025, 15(6), 2886; https://doi.org/10.3390/app15062886 - 7 Mar 2025
Abstract
This article proposes a displacement reducer based on distributed compliant mechanisms to improve the motion resolution of actuators commonly used in precision operation systems that require high-precision control and positioning, such as micro-grippers, biological manipulation, and micro-alignment mechanisms. Distributed compliance significantly diminishes its [...] Read more.
This article proposes a displacement reducer based on distributed compliant mechanisms to improve the motion resolution of actuators commonly used in precision operation systems that require high-precision control and positioning, such as micro-grippers, biological manipulation, and micro-alignment mechanisms. Distributed compliance significantly diminishes its effective moving lumped mass, endowing the structure with advantages such as reduced stress concentration and an expansive range of motion. Additionally, the design incorporates an over-constraint structure through a dual-layer displacement reducer, ensuring that the reducer achieves a nearly constant reduction ratio. According to the compliance matrix method, the analytical model of the reducer is established to predict the input–output behaviors, which are verified by finite element simulations. On the basis of sensitivity analysis to structure parameters, including node positions and beam parameters, the Particle Swarm Optimization (PSO) algorithm is used to optimize the displacement reduction performance. Through finite element analysis and experimental results on the prototype, the proposed displacement reducer demonstrates a large reduction ratio of 11.03, an energy transfer efficiency of 39.6%, and a nearly constant reduction ratio with an input displacement range of 0 to 2000 µm. Full article
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<p>Design procedure of the displacement reducer based on over-constraint: (<b>a</b>) A reducer designed based on triangular mechanical amplifier labeled by <math display="inline"><semantics> <mrow> <mi>D</mi> <mi>A</mi> <msup> <mi>D</mi> <mo>′</mo> </msup> </mrow> </semantics></math>; (<b>b</b>) Added two triangular levers by <math display="inline"><semantics> <mrow> <mi>D</mi> <mi>E</mi> <mi>G</mi> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <msup> <mi>D</mi> <mo>′</mo> </msup> <msup> <mi>E</mi> <mo>′</mo> </msup> <msup> <mi>G</mi> <mo>′</mo> </msup> </mrow> </semantics></math>; (<b>c</b>) Internal secondary reduction mechanism constructed on the same principle; (<b>d</b>) The final structure of the combined internal and external displacement reducer.</p>
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<p>Definition of coordinate frame for a single strip beam.</p>
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<p>Model geometry analysis chart.</p>
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<p>Local coordinate diagram.</p>
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<p>Mesh generation of the structure.</p>
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<p>Comparison of the predicted results between the kinetostatic model and FEA: (<b>a</b>) Input and output displacements; (<b>b</b>) The input displacement and the input force.</p>
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<p>Analysis results in ANSYS: (<b>a</b>) Stress distribution results in ANSYS; (<b>b</b>) Deformation results in ANSYS.</p>
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<p>Analysis of the influence of different points in the x−coordinates on the reduction ratio: (<b>a</b>) point <span class="html-italic">A</span>, (<b>b</b>) point <span class="html-italic">B</span>, (<b>c</b>) point <span class="html-italic">C</span>, (<b>d</b>) point <span class="html-italic">D</span>, (<b>e</b>) point <span class="html-italic">F</span>, (<b>f</b>) point <span class="html-italic">G</span>, (<b>g</b>) point <span class="html-italic">H</span>, (<b>h</b>) the relative position of points <span class="html-italic">C</span> and <span class="html-italic">D</span>.</p>
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<p>Analysis of the influence of different points in the y−coordinates on the reduction ratio: (<b>a</b>) point <span class="html-italic">A</span>, (<b>b</b>) point <span class="html-italic">B</span>, (<b>c</b>) point <span class="html-italic">C</span>, (<b>d</b>) point <span class="html-italic">D</span>, (<b>e</b>) point <span class="html-italic">F</span>, (<b>f</b>) point <span class="html-italic">G</span>, (<b>g</b>) point <span class="html-italic">H</span>, (<b>h</b>) the relative position of points <span class="html-italic">A</span> and <span class="html-italic">B</span>.</p>
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<p>Local sensitivity analysis of point and width: (<b>a</b>) The local sensitivity of point; (<b>b</b>) The local sensitivity of width.</p>
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<p>Constant maximum stiffness range along the Y-axis: (<b>a</b>) Fitness values; (<b>b</b>) Optimized structure; (<b>c</b>) Comparison of stiffness before and after optimization.</p>
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<p>Minimize the Y-axis displacement: (<b>a</b>) Fitness values. (<b>b</b>) Optimized structure. (<b>c</b>) Comparison of output displacement before and after optimization.</p>
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<p>Maximum energy transfer efficiency: (<b>a</b>) Fitness values; (<b>b</b>) Optimized structure; (<b>c</b>) Comparison of energy transfer efficiency before and after optimization.</p>
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<p>Fitness values.</p>
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<p>Optimized structure.</p>
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<p>The input–output displacement relationship.</p>
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<p>The shapes of the first 4 modes of the displacement reducer: (<b>a</b>) 1st Mode; (<b>b</b>) 2nd Mode; (<b>c</b>) 3rd Mode; (<b>d</b>) 4th Mode.</p>
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<p>Experimental testing setup: (<b>a</b>) The prototype displacement reducer; (<b>b</b>) The experimental devices.</p>
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<p>The experimental results of the displacement reducer: (<b>a</b>) The input–output displacement relationship in the range of 0 to 4000 µm; (<b>b</b>) The input–output reduction ratio in the range of 0 to 4000 µm; (<b>c</b>) Zoom in on the image from (<b>a</b>), 0 to 2000 µm; (<b>d</b>) Zoom in on the image from (<b>b</b>), 0 to 2000 µm.</p>
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<p>Reduction ratio under different loads.</p>
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<p>The displacement and force: (<b>a</b>) The output displacement and the output force; (<b>b</b>) The input displacement and the input force.</p>
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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
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)
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<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>
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<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>
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<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>
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<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>
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<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>
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<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>
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<p>Predicted tertiary structure of BraSWEET proteins.</p>
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<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>
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<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>
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<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>
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<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>
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<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>
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<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>
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29 pages, 6438 KiB  
Article
Potato Cultivation Under Zero Tillage and Straw Mulching: Option for Land and Cropping System Intensification for Indian Sundarbans
by Saikat Dey, Sukamal Sarkar, Anannya Dhar, Koushik Brahmachari, Argha Ghosh, Rupak Goswami and Mohammed Mainuddin
Land 2025, 14(3), 563; https://doi.org/10.3390/land14030563 - 7 Mar 2025
Abstract
Agriculture in the Indian Sundarbans deltaic region primarily depends on a rice-based monocropping system during the rainy season, with the subsequent season often remaining fallow. To mitigate this issue, a series of experiments using zero tillage and straw mulching (ZTSM) potato cultivation were [...] Read more.
Agriculture in the Indian Sundarbans deltaic region primarily depends on a rice-based monocropping system during the rainy season, with the subsequent season often remaining fallow. To mitigate this issue, a series of experiments using zero tillage and straw mulching (ZTSM) potato cultivation were conducted over eight consecutive years (2017–2024) across various islands in the Sundarbans Delta, West Bengal, aimed to intensify the cropping system and ensure the betterment of the land use pattern using climate-smart agricultural practices. In the initial two years, the experiments concentrated on assessing different potato cultivars and nutrient dosages under zero tillage and paddy straw mulching conditions. During the subsequent years, the focus shifted to field demonstrations under diverse climatic conditions. The research included the application of different macronutrients and growth regulators, in combination with different depths of straw mulching. In the final years of the study, the intervention was dedicated solely to the horizontal expansion of cultivated land. These initiatives aimed to enhance agricultural productivity and sustainable land use in the polders, promoting climate-resilient farming practices. From the sets of experiments, we standardized the sustainable nutrient management strategies and selection of appropriate potato cultivars vis-à-vis depth of straw mulching and, finally, the overall best agronomic practices for the region. The adoption of the ZTSM potato cultivation system demonstrated considerable success, as evidenced by the remarkable increase in the number of farmers employing this sustainable agricultural practice. The number of farmers practicing zero tillage potato cultivation surged from 23 in the initial year to over 1100, covering an area of more than 15 ha, highlighting the effectiveness of the technology. The analysis of the estimated adoption also showed that more than 90% adoption is likely to be achieved within a decade. This potential expansion underscores the benefits of the ZTSM potato cultivation system in improving soil health, conserving water, and reducing labour and costs. As more farmers recognize the advantages of zero tillage potato mulching, this approach is poised to play a pivotal role in sustainable agriculture, enhancing productivity while promoting environmental stewardship. Full article
(This article belongs to the Special Issue Tillage Methods on Soil Properties and Crop Growth)
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<p>Working principle of zero-tillage potato cultivation with paddy straw mulching (image created with <a href="https://BioRender.com" target="_blank">https://BioRender.com</a>; license no: BE27A0036T, accessed on 7 September 2024).</p>
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<p>(<b>a</b>) Plant height (cm); (<b>b</b>) the number of main branches/plants; (<b>c</b>) plant dry weight/plant, and (<b>d</b>) tuber dry weights/plants of different varieties of potatoes under ZTSM condition (where V1 = <span class="html-italic">K. chandramukhi</span>, V2 = <span class="html-italic">K. jyoti</span>, V3 = <span class="html-italic">S-52</span>, V4 = S6, and V5 = local).</p>
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<p>Effect of foliar nutrient management on (<b>a</b>) plant height, (<b>b</b>) number of compound leaves/plant, (<b>c</b>) leaf area index, and (<b>d</b>) total biomass per plant of ZTSM system of potato (T1: Control; T2: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 DAP</sub>; T3: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub>; T4: RDF<sub>NPK</sub> fb MOP 2% fs <sub>30 DAP</sub>; T5: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub> + MOP 2% fs <sub>30 DAP</sub>; T6: RDF<sub>NPK</sub> fb Boron 0.1% fs <sub>30 DAP</sub>; T7: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub> + Boron 0.1% fs <sub>30 DAP</sub>; T8: RDF<sub>NPK</sub> fb Zinc 0.5% fs <sub>30 DAP</sub>; T9: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub> + Zinc 0.5% fs <sub>30 DAP</sub>).</p>
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<p>Effects of biostimulants on (<b>a</b>) plant height; (<b>b</b>) number of compound leaves/plant; (<b>c</b>) leaf area index; and (<b>d</b>) total biomass/plant of ZTSM potato (where T1: Control, T2: RDF<sub>NPK</sub> fb <span class="html-italic">Sargassum</span> 5% fs <sub>30 DAP</sub>; T3: RDF<sub>NPK</sub> fb Sargassum 5% fs <sub>30 DAP &amp; 50 DAP</sub>; T4: RDF<sub>NPK</sub> fb Sargassum + humic acid 5% fs <sub>30 DAP</sub>; T5: RDF<sub>NPK</sub> fb Sargassum + humic acid 5% fs <sub>30 DAP &amp; 50 DAP</sub>; T6: RDF<sub>NPK</sub> fb Triacontanol 0.05% fs <sub>30 DAP</sub>; T7: RDF<sub>NPK</sub> fb Triacontanol 0.05% fs <sub>30 DAP &amp; 50 DAP</sub>; T8: Water).</p>
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<p>Effects of foliar nutrient and growth regulators on (<b>a</b>) plant height; (<b>b</b>) the number of compound leaves; (<b>c</b>) leaf area index; and (<b>d</b>) total biomass/plant (where T1: Water Spray; T2: 2% DAP at 30 DAP; T3: 2% DAP at 30 And 50 DAP; T4: 2% MOP at 30 DAP; T5: 2% MOP at 30 and 50 DAP; T6: 2% DAP and 2% MOP at 30 DAP; T7: 2% DAP and 2% MOP At 30 and 50 DAP; T8: 2% DAP + 2% MOP + 0.1% Triacontanol 0.05% EC (Miraculan) at 30 and 50 DAP).</p>
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<p>Effect of foliar nutrient management on (<b>a</b>) tuber hardness; (<b>b</b>) specific gravity; (<b>c</b>) pH; (<b>d</b>) vitamin C; (<b>e</b>) TSS; and (<b>f</b>) acidity of potatoes. T1: Control; T2: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 DAP</sub>; T3: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub>; T4: RDF<sub>NPK</sub> fb MOP 2% fs <sub>30 DAP</sub>; T5: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub> + MOP 2% fs <sub>30 DAP</sub>; T6: RDF<sub>NPK</sub> fb Boron 0.1% fs <sub>30 DAP</sub>; T7: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub> + Boron 0.1% fs <sub>30 DAP</sub>; T8: RDF<sub>NPK</sub> fb Zinc 0.5% fs <sub>30 DAP</sub>; T9: RDF<sub>NPK</sub> fb Urea 2% fs <sub>30 &amp; 50 DAP</sub> + Zinc 0.5% fs <sub>30 DAP</sub>.</p>
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<p>Effect of biostimulants on (<b>a</b>) acidity; (<b>b</b>) tuber hardness; (<b>c</b>) specific gravity; (<b>d</b>) pH; (<b>e</b>) vitamin C; (<b>f</b>) TSS of potatoes (where T1: Control, T2: RDF<sub>NPK</sub> fb Sargassum 5% fs <sub>30 DAP</sub>; T3: RDF<sub>NPK</sub> fb Sargassum 5% fs <sub>30 DAP &amp; 50 DAP</sub>; T4: RDF<sub>NPK</sub> fb Sargassum + humic acid 5% fs <sub>30 DAP</sub>; T5: RDF<sub>NPK</sub> fb Sargassum + humic acid 5% fs <sub>30 DAP &amp; 50 DAP</sub>; T6: RDF<sub>NPK</sub> fb Triacontanol 0.05% fs <sub>30 DAP</sub>; T7: RDF<sub>NPK</sub> fb Triacontanol 0.05% fs <sub>30 DAP &amp; 50 DAP</sub>; T8: Water).</p>
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<p>Effect of foliar nutrient and growth regulators on (<b>a</b>) tuber hardness; (<b>b</b>) specific gravity; (<b>c</b>) pH (<b>d</b>) vitamin C; (<b>e</b>) TSS; (<b>f</b>) pH of potatoes (where, T1: Water Spray; T2: 2% DAP at 30 DAP; T3: 2% DAP at 30 And 50 DAP; T4: 2% MOP at 30 DAP; T5: 2% MOP at 30 and 50 DAP; T6: 2% DAP and 2% MOP at 30 DAP; T7: 2% DAP and 2% MOP At 30 and 50 DAP; T8: 2% DAP + 2% MOP + 0.1% Triacontanol 0.05% EC (Miraculan) at 30 and 50 DAP).</p>
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<p>Comparison of soil moisture (%) between (<b>a</b>) zero-tilled–mulched potato fields and adjacent (<b>b</b>) fallow rice fields (vertical bars indicate the standard deviation of the mean).</p>
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<p>Comparison of soil salinity between (<b>a</b>) zero-tilled–mulched potato fields and adjacent (<b>b</b>) fallow rice fields (vertical bars indicate the standard deviation of the mean).</p>
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<p>Location and spatial distribution of ZTSM potato field across the various experimental sites of Indian Sundarbans (Site-I: Rangabelia, Site-II: Choto Mollakhali, and Site-III: Satjelia).</p>
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<p>Probability of exceedance (0–1) of potato tuber yield (kg/ha) across different locations in (<b>a</b>) <span class="html-italic">Rabi</span>, 2022, and (<b>b</b>) <span class="html-italic">Rabi</span>, 2023.</p>
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<p>Peak adoption level (%) and peak time to adoption (year) for zero tillage and straw mulching (ZTSM) potato cultivation for three scenarios. Scenarios are defined by the perceived “step-up” and “step-down” options of the ADOPT model. The figures on the right of the dotted vertical line suggest the likely rate of adoption in the first five years.</p>
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21 pages, 1939 KiB  
Review
Innovative Thermal Stabilization Methods for Expansive Soils: Mechanisms, Applications, and Sustainable Solutions
by Abdullah H. Alsabhan and Wagdi Hamid
Processes 2025, 13(3), 775; https://doi.org/10.3390/pr13030775 - 7 Mar 2025
Abstract
The thermal stabilization of expansive soils has emerged as a promising and sustainable alternative to conventional chemical stabilization methods, addressing the long-standing challenges associated with soil swelling and shrinkage. This review critically evaluates the mechanisms, applications, and advancements in thermal stabilization techniques, with [...] Read more.
The thermal stabilization of expansive soils has emerged as a promising and sustainable alternative to conventional chemical stabilization methods, addressing the long-standing challenges associated with soil swelling and shrinkage. This review critically evaluates the mechanisms, applications, and advancements in thermal stabilization techniques, with a particular focus on both traditional approaches (e.g., kiln heating) and emerging innovations such as microwave heating. This study synthesizes recent research findings to assess how thermal treatment modifies the mineralogical, physical, and mechanical properties of expansive soils, reducing their plasticity and improving their strength characteristics. Comparative analysis highlights the advantages, limitations, and sustainability implications of different thermal methods, considering factors such as energy efficiency, scalability, and environmental impact. While thermal stabilization offers a viable alternative to chemical treatments, key challenges remain regarding cost, field implementation, and long-term performance validation. The integration of thermal treatment with complementary techniques, such as lime stabilization, is explored as a means to enhance soil stability while minimizing environmental impact. By addressing critical research gaps and providing a comprehensive perspective on the future potential of thermal stabilization, this review contributes valuable insights for researchers and engineers seeking innovative and sustainable solutions for managing expansive soils. Full article
(This article belongs to the Special Issue 1st SUSTENS Meeting: Advances in Sustainable Engineering Systems)
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<p>Methods for stabilizing expansive soils.</p>
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<p>Factors influencing soil expansiveness.</p>
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<p>Illustration depicting moisture content in the active zone with and without the presence of a moisture barrier (adapted from [<a href="#B44-processes-13-00775" class="html-bibr">44</a>]).</p>
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<p>Construction process of the soil model [<a href="#B59-processes-13-00775" class="html-bibr">59</a>]: (<b>a</b>) sampling, (<b>b</b>) filling, (<b>c</b>) stilling, and (<b>d</b>) molding.</p>
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<p>Effect of microwave heating on expansive soil properties [<a href="#B8-processes-13-00775" class="html-bibr">8</a>]: (<b>a</b>) change in liquid limit and plastic limit with heating duration, (<b>b</b>) change in free swelling ratio with heating duration.</p>
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