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23 pages, 6631 KiB  
Article
Design of a Suspension Controller with Human Body Model for Ride Comfort Improvement and Motion Sickness Mitigation
by Jinwoo Kim and Seongjin Yim
Actuators 2024, 13(12), 520; https://doi.org/10.3390/act13120520 (registering DOI) - 16 Dec 2024
Abstract
This paper presents a method to design a suspension controller with a human body model for ride comfort improvement and motion sickness mitigation. Generally, it has been known that the vertical acceleration of a sprung mass should be reduced for ride comfort. On [...] Read more.
This paper presents a method to design a suspension controller with a human body model for ride comfort improvement and motion sickness mitigation. Generally, it has been known that the vertical acceleration of a sprung mass should be reduced for ride comfort. On the other hand, recent studies have shown that, combined, the vertical acceleration and pitch rate of a sprung mass are key factors that cause motion sickness. However, those variables have been considered with respect to the center of gravity of a sprung mass. For motion sickness mitigation, the vertical acceleration of a human head should be also considered. In this paper, the vertical accelerations and pitch rates of a sprung mass and a human head are controlled by a suspension controller for ride comfort improvement and motion sickness mitigation. For the controller design, a half-car and human body models are adopted. With those models, several types of static output feedback suspension controller are designed with linear quadratic optimal control methodology. To reduce the pitch rate of the sprung mass and the vertical acceleration of the head, a filtered-X LMS algorithm is adopted as an adaptive feedforward algorithm and combined with the static output feedback controllers. A frequency response analysis and simulation are performed with the designed controllers on vehicle simulation software, CarSim®. From the simulation results, it is shown that the proposed controllers can effectively reduce the vertical accelerations and the pitch rate of the sprung mass and the human head. Full article
(This article belongs to the Section Actuators for Land Transport)
16 pages, 4094 KiB  
Article
Study of the Biogas Ebullition from Lacustrine Carbonate Enriched and Black Silt Bottom Sediments
by Evaldas Maceika, Laima Kazakevičiūtė-Jakučiūnienė, Zita Žukauskaitė, Nina Prokopčiuk, Marina Konstantinova, Vadimas Dudoitis and Nikolay Tarasiuk
Water 2024, 16(24), 3608; https://doi.org/10.3390/w16243608 - 15 Dec 2024
Viewed by 312
Abstract
The greenhouse effect, which is also promoted by naturally occurring biogas ebullition fluxes (released via bubbles), generated by the decomposition of organic matter in carbonate-enriched and black silt sediments, has been analyzed. This study is based on results obtained using passive gas collectors [...] Read more.
The greenhouse effect, which is also promoted by naturally occurring biogas ebullition fluxes (released via bubbles), generated by the decomposition of organic matter in carbonate-enriched and black silt sediments, has been analyzed. This study is based on results obtained using passive gas collectors at different parts of eutrophic Lake Juodis, located in a temperate climate zone in the vicinity of Vilnius (Lithuania). The measured annual biogas (containing about 60% of biomethane) ebullition fluxes from carbonate-enriched sediments and black silt sediments were 16.9–23.0 L/(m2∙y) and 38.5–43.2 L/(m2∙y), respectively. This indicates that the gas fluxes from carbonate sediments were almost twice as low as those from black silt sediments. Oxygen, produced by the photosynthetic activity of green algae in the near-surface water and sediments, helps to retain carbonates in the sediments by preventing their dissolution. In turn, the calcite coating on sediment particles partially preserves organic matter from decomposition, reducing the effective thickness of the sediment layer generating biogas. The characteristic vertical distribution profile of 137Cs activity, with sharp peaks in sediments, suggests that generated biogas bubbles move to the surface of the sediments forming vertical channels by pushing sediment particles asides without noticeably mixing them vertically. This examination showed that factors such as abundance of carbonates in the sediments may result in a significant reduction in biogas generation and emissions from the lake sediments. Full article
(This article belongs to the Section Water Quality and Contamination)
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<p>Scheme of the biogas (methane) sampling sites (N1–N13) (●) using the “Jellyfish” apparatus on 8 August 2003 in Lake Juodis and the location of the northern (×) and southern stations (+) on a shallow bottom terrace. Carbonate sediment N1 and N2 (●) were sampled near the northern station (×); black silt sediment N3 (●) was sampled near the southern station (+); inflow and outflow of the brook (←).</p>
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<p>Microscopic photographs of the extracted sediment samples: (<b>a</b>) black silt, typically containing a large amount of decomposing organic matter and trapped biogas bubbles; (<b>b</b>) carbonate sediments, containing remnants of green algae.</p>
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<p>Vertical profiles of oxygen concentrations (mg/L) in the northern part of the lake in the green algae area (northern station) on 19 August 2003 (<b>a</b>) (bottom depth~122 cm), 3 November 2003 (<b>b</b>) (bottom depth~120 cm), and 16 March 2004 (<b>c</b>) (bottom depth~115 cm, the transparent ice thickness of ~32 cm).</p>
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<p>Vertical profile of oxygen concentrations (mg/L) in the northern part of the lake in the area of black silt sediments (southern station) on 11 August 2004 (<b>a</b>) (bottom depth~141 cm) and 13 October 2004 (<b>b</b>) (bottom depth~147 cm).</p>
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<p>Vertical profiles of <sup>137</sup>Cs activity concentration (<b>a</b>) and sediment density (<b>b</b>) in sample N1 of bottom sediments (rich in carbonate deposits) collected on 16 July 2003 near the northern sampling station (×) at a depth of 110 cm.</p>
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<p>Vertical profiles of <sup>137</sup>Cs activity concentration (<b>a</b>) and sediment density (<b>b</b>) in the sample N2 of bottom sediments (rich in carbonate deposits) collected on 16 July 2003 near the northern sampling station (×) at a depth of 120 cm.</p>
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<p>Vertical profiles of <sup>137</sup>Cs activity concentration (<b>a</b>) and sediment density (<b>b</b>) in the sample of black silt deposits (N3) taken on 29 August 2003 near the southern sampling station (+) at a depth of 140 cm.</p>
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<p>Biogas ebullition flux (L/m<sup>2</sup>∙s) from 18 September 2005 to 19 May 2007 (<b>a</b>) and from 8 October 2008 to 6 October 2010 (<b>b</b>) at the northern station (carbonate sediments).</p>
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<p>Biogas ebullition flux (L/m<sup>2</sup>∙s) from 18 September 2005 to 6 August 2007 (<b>a</b>) and from 8 October 2008 to 19 October 2010 (<b>b</b>) at the southern station (black silt sediments).</p>
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10 pages, 446 KiB  
Article
Genetic Analysis of Days Open in Moroccan Holstein Using Different Models to Account for Censored Data
by Narjice Chafai and Bouabid Badaoui
Animals 2024, 14(24), 3614; https://doi.org/10.3390/ani14243614 - 15 Dec 2024
Viewed by 273
Abstract
Reproductive efficiency is a key element of profitability in dairy herds. However, the genetic evaluation of fertility traits is often challenged by the presence of high censorship rates due to various reasons. An easy approach to address this challenge is to remove the [...] Read more.
Reproductive efficiency is a key element of profitability in dairy herds. However, the genetic evaluation of fertility traits is often challenged by the presence of high censorship rates due to various reasons. An easy approach to address this challenge is to remove the censored data from the dataset. However, removing data might bias the genetic evaluation. Therefore, addressing this issue is crucial, particularly for small populations and populations with limited size. This study uses a Moroccan Holstein dataset to compare two Gaussian linear models and a threshold linear model to handle censored records of days open (DO). Data contained 8646 records of days open across the first three parities of 6337 Holstein cows. The pedigree file comprised 11,555 animals and 14.51% of the dataset was censored. The genetic parameters and breeding values of DO were computed using three different methods: a linear model where all censored records were omitted (LM), a penalty method in which a constant equal to one estrus cycle in cattle was added to the maximum value of DO in each contemporary group to impute the censored records (PLM), and a bivariate threshold model with a penalty (PTM). The heritability estimates were equal to 0.021 ± 0.01 (PLM), 0.029 ± 0.01 (LM), and 0.033 ± 0.01 (PTM). The penalty method and the threshold linear model with a penalty showed better prediction accuracy calculated using the LR method (0.21, and 0.20, respectively). PLM and PTM had a high Spearman correlation (0.99) between the estimated breeding values of the validation dataset, which explains the high percentage of common animals in the top 20% of selected animals. The lack of changes in the ranking of animals between PLM and PTM suggests that both methods can be used to address censored data in this population. Full article
(This article belongs to the Collection Applications of Quantitative Genetics in Livestock Production)
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<p>The distribution of days open (DO) across the three first parties.</p>
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10 pages, 8466 KiB  
Article
Investigation of a Robust Blind Deconvolution Algorithm Using Extracted Structures in Light Microscopy Images of Salivary Glands: A Pilot Study
by Kyuseok Kim, Jae-Young Kim and Ji-Youn Kim
Electronics 2024, 13(24), 4940; https://doi.org/10.3390/electronics13244940 (registering DOI) - 14 Dec 2024
Viewed by 329
Abstract
Although light microscopy (LM) images are widely used to observe various bodily tissues, including salivary glands, reaching a satisfactory spatial resolution in the final images remains a major challenge. The objective of this study was to model a robust blind deconvolution algorithm using [...] Read more.
Although light microscopy (LM) images are widely used to observe various bodily tissues, including salivary glands, reaching a satisfactory spatial resolution in the final images remains a major challenge. The objective of this study was to model a robust blind deconvolution algorithm using the extracted structure and analyze its applicability to LM images. Given LM images of the salivary glands, the proposed robust blind deconvolution method performs non-blind deconvolution after estimating the structural map and kernel of each image. To demonstrate the usefulness of the proposed algorithm for LM images, the perceptual sharpness index (PSI), Blanchet’s sharpness index (BSI), and natural image quality evaluator (NIQE) were used as evaluation metrics. We demonstrated that when the proposed algorithm was applied to salivary gland LM images, the PSI and BSI were improved by 7.95% and 7.44%, respectively, compared with those of the conventional TV-based algorithm. When the proposed algorithm was applied to an LM image, we confirmed that the NIQE value was similar to that of a low-resolution image. In conclusion, the proposed robust blind deconvolution algorithm is highly applicable to salivary gland LM images, and we expect that further applications will become possible. Full article
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<p>Simplified framework of a robust blind deconvolution method using a structural map to estimate the blur kernel in a light microscopy image.</p>
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<p>Low-resolution image of the salivary gland obtained via light microscopy (scale bar = 200 μm, <math display="inline"><semantics> <mrow> <mo>×</mo> </mrow> </semantics></math>100 magnification) (<b>top</b>), and restored images obtained by the total variation (TV)-based (<b>middle</b>) and proposed (<b>bottom</b>) algorithms. A distortion effect can be observed following restoration by the TV-based algorithm.</p>
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<p>Low-resolution image of the salivary gland obtained via light microscopy (scale bar = 50 μm, <math display="inline"><semantics> <mrow> <mo>×</mo> </mrow> </semantics></math>400 magnification) (<b>left</b>), and restored images obtained by the TV-based (<b>middle</b>) and proposed (<b>right</b>) algorithms. As a result of enlarging and observing areas where blurring occurred, it was confirmed that the TV-based algorithm incurs significant image distortion.</p>
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<p>(<b>a</b>) Perceptual sharpness index (PSI) and (<b>b</b>) Blanchet’s sharpness index (BSI) results measured from light microscopy images obtained for original images and reconstructions by the TV-based and proposed algorithms. Images reconstructed by the proposed algorithm exhibited superior PSI and BSI values compared to the original images and TV-based reconstructions.</p>
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<p>Natural image quality evaluator (NIQE) results measured from light microscopy images, obtained for original images and reconstructions by the TV-based and proposed algorithms. Although the original image exhibited the best NIQE results, the reconstruction obtained by the proposed algorithm also achieved excellent results.</p>
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14 pages, 2882 KiB  
Article
Proteomic Analysis of the Fish Pathogen Vibrio ordalii Strain Vo-LM-18 and Its Outer Membrane Vesicles
by Macarena Echeverría-Bugueño, Mauricio Hernández and Ruben Avendaño-Herrera
Animals 2024, 14(24), 3598; https://doi.org/10.3390/ani14243598 - 13 Dec 2024
Viewed by 318
Abstract
Vibrio ordalii is the causative agent of atypical vibriosis in salmonids cultured in Chile. While extensive research provides insights into V. ordalii through phenotypic, antigenic, and genetic typing, as well as various virulence mechanisms, proteomic characterization remains largely unexplored. This study aimed to [...] Read more.
Vibrio ordalii is the causative agent of atypical vibriosis in salmonids cultured in Chile. While extensive research provides insights into V. ordalii through phenotypic, antigenic, and genetic typing, as well as various virulence mechanisms, proteomic characterization remains largely unexplored. This study aimed to advance the proteomic knowledge of Chilean V. ordalii Vo-LM-18 and its OMVs, which have known virulence. Using Nano-UHPLC-LC-MS/MS, we identified 2242 proteins and 1755 proteins in its OMVs. Of these, 644 unique proteins were detected in V. ordalii Vo-LM-18, namely 156 unique proteins in its OMVs and 1596 shared proteins. The major categories for the OMVs were like those in the bacteria (i.e., cytoplasmic and cytoplasmic membrane proteins). Functional annotation identified 37 biological pathways in V. ordalii Vo-LM-18 and 28 in its OMVs. Proteins associated with transport, transcription, and virulence were predominant in both. Evident differences in protein expression were found. OMVs expressed a higher number of virulence-associated proteins, including those related to iron- and heme-uptake mechanisms. Notable pathways in the bacteria included flagellum assembly, heme group-associated proteins, and protein biosynthesis. This proteomic analysis is the first to detect the RTX toxin in a V. ordalii strain (Vo-LM-18) and its vesicles. Our results highlight the crucial role of OMVs in the pathogenesis and adaptation of V. ordalii, suggesting use as potential diagnostic biomarkers and therapeutic targets for bacterial infections. Full article
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<p>Characteristics of <span class="html-italic">Vibrio ordalii</span> Vo-LM-18 and its OMVs. SEM visualization of (<b>a</b>) the bacteria and (<b>c</b>) its OMVs. SEM-determined size of (<b>b</b>) the bacterium and (<b>d</b>) OMVs, showing greater heterogeneity in OMVs sizes vs. bacteria. Venn diagram illustrating proteins identified across each replicate of (<b>e</b>) <span class="html-italic">Vibrio ordalii</span> Vo-LM-18 and (<b>f</b>) its OMVs. The arrowhead points to the OMVs.</p>
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<p>Proteomic and protein subcellular localization resources (PSORT) analyses of <span class="html-italic">Vibrio ordalii</span> strain Vo-LM-18 and its OMVs. (<b>a</b>) Venn diagram showing the overlap of proteins identified in the Vo-LM-18 strain and its OMVs. (<b>b</b>) Distribution of proteins by cellular compartment as predicted by PSORT. (<b>c</b>) Functional categorization and grouping of proteins annotated by Gene Ontology.</p>
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<p>Graphic representation of the quantitative proteomic analysis of <span class="html-italic">Vibrio ordalii</span> Vo-LM-18 and its OMVs. (<b>a</b>) Principal component analysis (PCA) of quantifiable proteins from <span class="html-italic">Vibrio ordalii</span> Vo-LM-18 and its OMVs. (<b>b</b>) Heatmap displaying significantly differentially expressed proteins (DEPs) common to both the Vo-LM-18 strain and its OMVs, along with their functional distribution.</p>
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<p>Co-expression networks in <span class="html-italic">Vibrio ordalii</span> Vo-LM-18 and its OMVs. Each node represents a metabolic pathway, and the edges between nodes indicate subordinate relationships between different pathways. Proteins involved in each pathway are highlighted as either over-expressed (red) or under-expressed (blue).</p>
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17 pages, 8597 KiB  
Article
Automatic Segmentation of Metastatic Livers by Means of U-Net-Based Procedures
by Camilla Tiraboschi, Federica Parenti, Fabio Sangalli, Andrea Resovi, Dorina Belotti and Ettore Lanzarone
Cancers 2024, 16(24), 4159; https://doi.org/10.3390/cancers16244159 - 13 Dec 2024
Viewed by 250
Abstract
Background: The liver is one of the most common sites for the spread of pancreatic ductal adenocarcinoma (PDAC) cells, with metastases present in about 80% of patients. Clinical and preclinical studies of PDAC require quantification of the liver’s metastatic burden from several acquired [...] Read more.
Background: The liver is one of the most common sites for the spread of pancreatic ductal adenocarcinoma (PDAC) cells, with metastases present in about 80% of patients. Clinical and preclinical studies of PDAC require quantification of the liver’s metastatic burden from several acquired images, which can benefit from automatic image segmentation tools. Methods: We developed three neural networks based on U-net architecture to automatically segment the healthy liver area (HL), the metastatic liver area (MLA), and liver metastases (LM) in micro-CT images of a mouse model of PDAC with liver metastasis. Three alternative U-nets were trained for each structure to be segmented following appropriate image preprocessing and the one with the highest performance was then chosen and applied for each case. Results: Good performance was achieved, with accuracy of 92.6%, 88.6%, and 91.5%, specificity of 95.5%, 93.8%, and 99.9%, Dice of 71.6%, 74.4%, and 29.9%, and negative predicted value (NPV) of 97.9%, 91.5%, and 91.5% on the pilot validation set for the chosen HL, MLA, and LM networks, respectively. Conclusions: The networks provided good performance and advantages in terms of saving time and ensuring reproducibility. Full article
(This article belongs to the Special Issue Advanced Research in Pancreatic Ductal Adenocarcinoma)
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<p>Proposed architecture consisting of three CNNs: the healthy liver (HL) network, the metastatic liver area (MLA) network, and the liver metastases (LM) network.</p>
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<p>Healthy liver slice (<b>a</b>) and metastatic liver slice (<b>b</b>) in the sagittal (∼2600 × 1500 pixels), frontal (∼2600 × 1600 pixels), and transverse planes (∼1500 × 1600 pixels), visualized with open source software 3DSlicer (version 5.7) [<a href="#B22-cancers-16-04159" class="html-bibr">22</a>].</p>
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<p>Sample images of healthy liver for HL: proximal slice (<b>a</b>), slice in the middle (<b>b</b>), and distal slice (<b>c</b>). The acquired image, the corresponding GT, the HL segmentations before binarization, and the predicted BPMs from all networks (U-net-1, U-net-2, and U-net-3) are reported for each slice.</p>
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<p>Sample images of liver with metastases for MLA: proximal slice (<b>a</b>), slice in the middle (<b>b</b>), and distal slice (<b>c</b>). The acquired image, the corresponding GT, the MLA segmentations before binarization and the predicted BPMs from all networks (U-net-1, U-net-2, and U-net-3) are reported for each slice.</p>
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<p>Sample images of liver with metastases for LM: proximal slice (<b>a</b>), slice in the middle (<b>b</b>), and distal slice (<b>c</b>). The acquired image, the corresponding GT, the LM segmentations before binarization, and the predicted BPMs from all networks (U-net-1, U-net-2, and U-net-3) are reported for each slice.</p>
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<p>Comparison between the original U-net-3 for LM (<b>left</b>) and the alternative one based on the manually cleaned images (<b>right</b>): image and GT common to both alternatives, LM segmentation before binarization, and predicted BPM.</p>
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<p>Examples of a combined mask: BPM for metastases in yellow and metastatic liver surface in blue (<b>a</b>); GT with metastases in fuchsia and metastatic liver surface in blue (<b>b</b>).</p>
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17 pages, 1043 KiB  
Article
Can Different Dietary Protein Sources Influence the Survival, Growth, and Physiology of 0+Marron (Cherax cainii) Exposed to Feed Deprivation?
by Thi Thanh Thuy Dao and Ravi Fotedar
Animals 2024, 14(24), 3591; https://doi.org/10.3390/ani14243591 - 12 Dec 2024
Viewed by 471
Abstract
We investigated the effect of feed deprivation for 45 days on the growth, immunity, and health of 0+marron (Cherax cainii) initially fed for 110 days on various protein sources including fishmeal (FM), poultry by-product meal (PBM), black soldier fly [...] Read more.
We investigated the effect of feed deprivation for 45 days on the growth, immunity, and health of 0+marron (Cherax cainii) initially fed for 110 days on various protein sources including fishmeal (FM), poultry by-product meal (PBM), black soldier fly meal (BSFM), soybean meal (SBM), lupin meal (LM), and tuna hydrolysate. The marron were weighed and sacrificed immediately after feeding stopped (day 0) and at days 15, 30, and 45 after the feed deprivation trial commenced. Total haemolymph count, differential haemocyte count, lysozyme activity, protease activity, total bacterial count in the digestive tract, and organosomatic indices were analysed. Initially feeding marron any protein sources did not influence the percentage of weight gain and specific growth rates of marron. All marron showed more than 83% survival; however, marron fed soybean meal showed significantly lower survival than others. Dietary sources of protein altered organosomatic indices of starved marron during various starvation periods and resulted in a significant decrease in total haemocyte counts, lysozyme activity, protease activity, and bacterial count in the digestive tract of marron. Starved marron initially fed PBM and BSFM showed higher tolerance to starvation, followed by marron initially fed FM and SBM, while marron initially fed TH and LM showed the highest susceptibility to starvation. Full article
(This article belongs to the Section Aquatic Animals)
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<p>The survival rate of the marron fed test diet during the starvation test. Mean ± SE (n = 3). ns indicates not significant. * <span class="html-italic">p</span> &lt; 0.05 denotes significant differences. SFM: starved marron initially fed fishmeal; SPBM: starved marron initially fed poultry by-product meal; SBSFM: starved marron fed initially black soldier fly meal; STH: starved marron initially fed tuna hydrolysate; SLM: starved marron initially fed lupin meal; SSBM: starved marron initially fed soybean meal.</p>
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<p>Lysozyme activity (<b>A</b>) and THC (<b>B</b>) in marron during feed deprivation. The values are mean ± SE (n = 3). Letters (A, B, C) indicate significantly different means for different groups at <span class="html-italic">p</span> &lt; 0.05. Different numbers (1, 2, 3) denote significantly different means at times of feed deprivation. Two-way ANOVA, followed by Tukey post hoc test at <span class="html-italic">p</span> &lt; 0.05 determined the effects of treatments on lysozyme, feed deprivation durations on lysozyme activity, and their interaction between treatments and feed deprivation durations. SFM: starved marron initially fed fishmeal; SPBM: starved marron initially fed poultry by-product meal; SBSFM: starved marron fed initially black soldier fly meal; STH: starved marron initially fed tuna hydrolysate; SLM: starved marron initially fed lupin meal; SSBM: starved marron initially fed soybean meal.</p>
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<p>Differential haemocyte count of starved marron during feed deprivation period. Granular cells (<b>A</b>), hyaline cells (<b>B</b>), and semi-granular cells (<b>C</b>). The values are mean ± SE (n = 3). Letters (A, B, C, D) indicate significantly different means for different groups at <span class="html-italic">p</span> &lt; 0.05. Different numbers (1, 2, 3, 4) denote significantly different means at different times of feed deprivation. Two-way ANOVA, followed by Tukey post hoc test at <span class="html-italic">p</span> &lt; 0.05 determined the effects of treatments on lysozyme, feed deprivation durations on lysozyme activity, and their interaction between treatments and feed deprivation durations. SFM: starved marron initially fed fishmeal; SPBM: starved marron initially fed poultry by-product meal; SBSFM: starved marron fed initially black soldier fly meal; STH: starved marron initially fed tuna hydrolysate; SLM: starved marron initially fed lupin meal; SSBM: starved marron initially fed soybean meal.</p>
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<p>The protease activity (<b>A</b>) and total bacterial count (<b>B</b>) of starved marron before and after feed deprivation. Two-way ANOVA, followed by Tukey post hoc test with <span class="html-italic">p</span> &lt; 0.05 determined the effects of treatments on lysozyme, feed deprivation durations on lysozyme activity, and their interaction between treatments and feed deprivation durations. Letters (A, B, C, D) represent significant differences among treatments. * <span class="html-italic">p</span> &lt; 0.05 indicates a significant difference before and after feed deprivation. ns denotes non-significant differences. A paired <span class="html-italic">t</span>-test determined the significant difference between the starved marron groups before and after feed deprivation. The line within each box represents the median. The results are expressed in mean ± SE (n = 3). The dots indicate the replicate (n).</p>
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14 pages, 3391 KiB  
Article
Comparative Study on Selenium and Volatile Compounds in Selenium-Enriched Cardamine violifolia Pickles Fermented by Three Distinct Methods
by Jue Gong, Shen Rao, Xiaomeng Liu, Shuiyuan Cheng, Xin Cong and Dingxiang Zhu
Fermentation 2024, 10(12), 632; https://doi.org/10.3390/fermentation10120632 - 11 Dec 2024
Viewed by 326
Abstract
Cardamine violifolia is a selenium (Se)-rich vegetable crop belonging to the Brassicaceae family. This study investigated the Se concentration and volatiles in the fresh (CK) C. violifolia, natural fermented (NF), Lactiplantibacillus plantarum (LP), and Leuconostoc mesenteroides (LM) fermented C. violifolia pickles. Results [...] Read more.
Cardamine violifolia is a selenium (Se)-rich vegetable crop belonging to the Brassicaceae family. This study investigated the Se concentration and volatiles in the fresh (CK) C. violifolia, natural fermented (NF), Lactiplantibacillus plantarum (LP), and Leuconostoc mesenteroides (LM) fermented C. violifolia pickles. Results showed that fermentation promoted the levels of selenocysteine, methyl selenocysteine, and selenate. A total of 648 volatile compounds were found, including 119 terpenoids, 105 heterocyclic compounds, 103 esters, and 65 hydrocarbons. Differential analysis of volatiles indicated that fermentation induced the release of volatiles when compared to CK, whereas volatile profiles in LM and NF pickles showed notable differences from LP pickles. SeCys2, MeSeCys, and selenate significantly correlated to several volatile compounds, implying that Se metabolism may affect the formation of volatiles. Conclusively, fermentation promoted the release of aroma and bioactive volatiles and the degradation of unpleasant and harmful substances in C. violifolia pickles. Full article
(This article belongs to the Section Fermentation for Food and Beverages)
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<p>Overview of the volatile compounds in fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) classification of the volatile compounds, (<b>B</b>) principal component analysis of the samples, and (<b>C</b>) concentration changes of the volatiles in each group. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control.</p>
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<p>Comprehensive analysis of the DVCs in fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) statistics of the DVCs in each comparison group, (<b>B</b>) classification of the DVCs, and (<b>C</b>) cluster analysis of the concentrations of DVCs. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control.</p>
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<p>Analysis of the DVCs between CK and fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) overlap of the three comparison groups; (<b>B</b>) classification of the 248 DVCs in the overlap; (<b>C</b>) overlap of the DVCs with a fold change greater than 10 in the three comparison groups; (<b>D</b>) K-means analysis of the 48 DVCs. Different color lines indicate different subclasses of compounds; (<b>E</b>) concentration changes of the nine DVCs in subclass 5 from the K-means analysis; and (<b>F</b>) concentration changes of the 13 top changed DVCs. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control.</p>
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<p>Analysis of DVCs between the fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) overlap of the two comparison groups; (<b>B</b>) concentration changes of the 40 DVCs in three pickles; (<b>C</b>) top changed DVCs in NF vs. LP comparison group; and (<b>D</b>) top changed DVCs in LM vs. LP comparison group. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control. XMW1398: methyl 5-hydroxynicotinate; XMW0533: 3-methylbenzothiophene; KMW0359: 3-ethyl-phenol; XMW0300: 3,5-dimethyl-phenol; KMW0469: 4-ethyl-2-methoxy-phenol; NMW0066: 2,4-dimethyl-benzenamine; D276: umbellulon; XMW0212: 1,4-benzodioxan-6-amine; NMW0193: 4-hydroxy-benzeneethanol; w21: 6-pentyl-2H-pyran-2-one; XMW0549: naphthalene.</p>
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<p>Correlation analysis between Se and volatile compounds detected in <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) correlation between SeCys<sub>2</sub> and volatile compounds; (<b>B</b>) correlation between MeSeCys and selenate and volatile compounds; and (<b>C</b>) correlation between Se and the representative volatile compounds.</p>
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18 pages, 1629 KiB  
Article
Exploring Feedback Design Perceptions and Relationships with Scores in the Online Component of an EAP-Blended Course
by Anna Moni, María-Jesús Martínez-Argüelles and Enric Serradell-López
Appl. Sci. 2024, 14(24), 11554; https://doi.org/10.3390/app142411554 - 11 Dec 2024
Viewed by 365
Abstract
This quantitative study investigates the perceptions of learners and faculty regarding the help provided by the feedback process, which aligns with and integrates Brooks et al.’s Matrix of Feedback for Learning in the asynchronous online component of a blended course and the relationship [...] Read more.
This quantitative study investigates the perceptions of learners and faculty regarding the help provided by the feedback process, which aligns with and integrates Brooks et al.’s Matrix of Feedback for Learning in the asynchronous online component of a blended course and the relationship between student perceptions and scores. The feedback process, integrated into 12 weekly learning modules in Blackboard Learn (LMS) in alignment with Quality Matters (QM) standards for higher online education, seeks to facilitate feedback uptake and support student learning. Results from the test analysis of student (N = 135) and faculty (N = 10) surveys indicated that positive learner perceptions of feedback, corroborated by institutional course evaluations, aligned with faculty perceptions, suggesting a shared understanding of feedback’s role in learning. Interestingly, these findings suggested that feedback was perceived as beneficial independently of academic performance, potentially showing a trend of growth in students’ academic mindset, where feedback becomes a critical component of their learning experience. Additionally, this study points out that the Matrix of Feedback for Learning could be applied across different disciplinary contexts. Full article
(This article belongs to the Special Issue The Application of Digital Technology in Education)
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<p>A Matrix of Feedback for Learning [<a href="#B15-applsci-14-11554" class="html-bibr">15</a>]. Reprinted with permission.</p>
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<p>A structured flow of instructional content and activities within each weekly learning cycle in the EAP asynchronous online component.</p>
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<p>Flowchart depicting the research design. Created by the authors.</p>
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25 pages, 5732 KiB  
Article
Analyzing the Impact of Binaural Beats on Anxiety Levels by a New Method Based on Denoised Harmonic Subtraction and Transient Temporal Feature Extraction
by Devika Rankhambe, Bharati Sanjay Ainapure, Bhargav Appasani, Avireni Srinivasulu and Nicu Bizon
Bioengineering 2024, 11(12), 1251; https://doi.org/10.3390/bioengineering11121251 - 10 Dec 2024
Viewed by 416
Abstract
Anxiety is a widespread mental health issue, and binaural beats have been explored as a potential non-invasive treatment. EEG data reveal changes in neural oscillation and connectivity linked to anxiety reduction; however, harmonics introduced during signal acquisition and processing often distort these findings. [...] Read more.
Anxiety is a widespread mental health issue, and binaural beats have been explored as a potential non-invasive treatment. EEG data reveal changes in neural oscillation and connectivity linked to anxiety reduction; however, harmonics introduced during signal acquisition and processing often distort these findings. Existing methods struggle to effectively reduce harmonics and capture the fine-grained temporal dynamics of EEG signals, leading to inaccurate feature extraction. Hence, a novel Denoised Harmonic Subtraction and Transient Temporal Feature Extraction is proposed to improve the analysis of the impact of binaural beats on anxiety levels. Initially, a novel Wiener Fused Convo Filter is introduced to capture spatial features and eliminate linear noise in EEG signals. Next, an Intrinsic Harmonic Subtraction Network is employed, utilizing the Attentive Weighted Least Mean Square (AW-LMS) algorithm to capture nonlinear summation and resonant coupling effects, effectively eliminating the misinterpretation of brain rhythms. To address the challenge of fine-grained temporal dynamics, an Embedded Transfo XL Recurrent Network is introduced to detect and extract relevant parameters associated with transient events in EEG data. Finally, EEG data undergo harmonic reduction and temporal feature extraction before classification with a cross-correlated Markov Deep Q-Network (DQN). This facilitates anxiety level classification into normal, mild, moderate, and severe categories. The model demonstrated a high accuracy of 95.6%, precision of 90%, sensitivity of 93.2%, and specificity of 96% in classifying anxiety levels, outperforming previous models. This integrated approach enhances EEG signal processing, enabling reliable anxiety classification and offering valuable insights for therapeutic interventions. Full article
(This article belongs to the Special Issue Adaptive Neurostimulation: Innovative Strategies for Stimulation)
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<p>Block Diagram of the proposed system.</p>
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<p>Wiener Fused Convo Filter.</p>
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<p>Flowchart of Hilbert–Huang transformation process of the proposed system.</p>
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<p>Attentive Weighted Least Mean Square (AW-LMS) algorithm of the proposed model.</p>
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<p>Schematic representation of a Transformer-XL.</p>
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<p>Long Short-Term Memory.</p>
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<p>Input EEG of the proposed model for (<b>a</b>) delta, (<b>b</b>) theta, (<b>c</b>) alpha, (<b>d</b>) beta, and (<b>e</b>) gamma.</p>
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<p>Input EEG of the proposed model for (<b>a</b>) delta, (<b>b</b>) theta, (<b>c</b>) alpha, (<b>d</b>) beta, and (<b>e</b>) gamma.</p>
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<p>Pre-processed EEG of the proposed model for (<b>a</b>) delta, (<b>b</b>) theta, (<b>c</b>) alpha, (<b>d</b>) beta, and (<b>e</b>) gamma.</p>
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<p>Normalized frequencies of the proposed model for (<b>a</b>) delta, (<b>b</b>) theta, (<b>c</b>) alpha, (<b>d</b>) beta, and (<b>e</b>) gamma.</p>
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<p>Brain rhythm of the proposed model for (<b>a</b>) delta, (<b>b</b>) theta, (<b>c</b>) alpha, (<b>d</b>) beta, and (<b>e</b>) gamma.</p>
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<p>The loss rate of the proposed system.</p>
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<p>Mean square error (MSE) of the proposed model.</p>
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<p>Confusion matrix of the proposed method.</p>
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<p>Accuracy, precision, sensitivity, specificity, and F1 score of the proposed model.</p>
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<p>FPR, FNR, and MAE of the proposed model.</p>
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<p>NPV, PSNR, and MCC of the proposed model.</p>
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<p>Comparison of key metrics such as accuracy, precision, sensitivity, specificity, and F1 score of the proposed model.</p>
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<p>Comparison of the NPV and MCC of the proposed model.</p>
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<p>Comparison of the FNR, FPR, and FDR of the proposed model.</p>
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21 pages, 3950 KiB  
Review
Generative AI in Medicine and Healthcare: Moving Beyond the ‘Peak of Inflated Expectations’
by Peng Zhang, Jiayu Shi and Maged N. Kamel Boulos
Future Internet 2024, 16(12), 462; https://doi.org/10.3390/fi16120462 - 9 Dec 2024
Viewed by 927
Abstract
The rapid development of specific-purpose Large Language Models (LLMs), such as Med-PaLM, MEDITRON-70B, and Med-Gemini, has significantly impacted healthcare, offering unprecedented capabilities in clinical decision support, diagnostics, and personalized health monitoring. This paper reviews the advancements in medicine-specific LLMs, the integration of Retrieval-Augmented [...] Read more.
The rapid development of specific-purpose Large Language Models (LLMs), such as Med-PaLM, MEDITRON-70B, and Med-Gemini, has significantly impacted healthcare, offering unprecedented capabilities in clinical decision support, diagnostics, and personalized health monitoring. This paper reviews the advancements in medicine-specific LLMs, the integration of Retrieval-Augmented Generation (RAG) and prompt engineering, and their applications in improving diagnostic accuracy and educational utility. Despite the potential, these technologies present challenges, including bias, hallucinations, and the need for robust safety protocols. The paper also discusses the regulatory and ethical considerations necessary for integrating these models into mainstream healthcare. By examining current studies and developments, this paper aims to provide a comprehensive overview of the state of LLMs in medicine and highlight the future directions for research and application. The study concludes that while LLMs hold immense potential, their safe and effective integration into clinical practice requires rigorous testing, ongoing evaluation, and continuous collaboration among stakeholders. Full article
(This article belongs to the Special Issue The Future Internet of Medical Things II)
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<p>AI-generated image and text description in response to the prompt “generate an image illustrating the different generative AI and LLM uses and applications in medicine and healthcare”. Note the malformed and misspelled text towards the top right part of the image (it was probably meant to read “personalized medicine”). This is a common observation with current models. Generator: OpenAI’s DALL·E 3, September 1, 2024; Requestor: Maged N. Kamel Boulos; License: Public Domain (CC0).</p>
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17 pages, 4293 KiB  
Article
A Gravity-Driven Membrane Bioreactor in Treating Real Fruit Juice Wastewater: Response Relationship Between Filtration Behavior and Microbial Community Evolution
by Dan Song, Haiyao Du, Shichun Chen, Xiaodie Han, Lu Wang, Yonggang Li, Caihong Liu, Wenjuan Zhang and Jun Ma
Membranes 2024, 14(12), 260; https://doi.org/10.3390/membranes14120260 - 6 Dec 2024
Viewed by 421
Abstract
The issue of environmental pollution caused by wastewater discharge from fruit juice production has attracted increasing attention. However, the cost-effectiveness of conventional treatment technology remains insufficient. In this study, a gravity-driven membrane bioreactor (GDMBR) was developed to treat real fruit juice wastewater from [...] Read more.
The issue of environmental pollution caused by wastewater discharge from fruit juice production has attracted increasing attention. However, the cost-effectiveness of conventional treatment technology remains insufficient. In this study, a gravity-driven membrane bioreactor (GDMBR) was developed to treat real fruit juice wastewater from secondary sedimentation at pressures ranging from 0.01 to 0.04 MPa without requiring backwashing or chemical cleaning, with the aim of investigating flux development and contaminant removal under low-energy conditions. The results demonstrate an initial decrease in flux followed by stabilization during long-term filtration. Moreover, the stabilized flux level achieved with the GDMBR at pressures of 0.01 and 0.02 MPa was observed to surpass that obtained at 0.04 MPa, ranging from 4 to 4.5 L/m−2 h−1. The stability of flux was positively associated with the low membrane fouling resistance observed in the GDMBR system. Additionally, the GDMBR system provided remarkable efficiencies in removing the chemical oxygen demand (COD), biological oxygen demand (BOD), ammonia (NH4+-N), and total nitrogen (TN), with average removal rates of 82%, 80%, 83%, and 79%, respectively. The high biological activity and microbial community diversity within the sludge and biofilm are expected to enhance its biodegradation potential, thereby contributing to the efficient removal of contaminants. Notably, a portion of total phosphorus (TP) can be effectively retained in the reactor, which highlighted the promising application of the GDMBR process for actual fruit juice wastewater based on these findings. Full article
(This article belongs to the Section Membrane Applications for Water Treatment)
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<p>Schematic diagram of the GDMBR system in treating fruit juice wastewater directly.</p>
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<p>(<b>a</b>) Variation in water flux with operation time; (<b>b</b>) stable flux; (<b>c</b>) variation in membrane resistances with operation time; and (<b>d</b>) stable membrane resistance during the operation.</p>
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<p>(<b>a</b>) COD concentrations in influent and effluent; (<b>b</b>) COD removal rates; (<b>c</b>) stable COD concentration in influent and effluent and stable removal efficiency; (<b>d</b>) BOD concentrations in influent and effluent; (<b>e</b>) BOD removal rates; (<b>f</b>) stable BOD concentration in influent and effluent and stable removal efficiency; (<b>g</b>) SS concentrations in influent and effluent; (<b>h</b>) SS removal rates; (<b>i</b>) stable SS concentration in influent and effluent and stable removal efficiency.</p>
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<p>(<b>a</b>) NH<sub>4</sub><sup>+</sup>-N concentrations in influent and effluent; (<b>b</b>) NH<sub>4</sub><sup>+</sup>-N removal rates; (<b>c</b>) stable NH<sub>4</sub><sup>+</sup>-N concentration in influent and effluent and stable removal efficiency; (<b>d</b>) TN concentrations in influent and effluent; (<b>e</b>) TN removal rates; (<b>f</b>) stable TN concentration in influent and effluent and stable removal efficiency; (<b>g</b>) TP concentrations in influent and effluent; (<b>h</b>) TP removal rates; and (<b>i</b>) stable TP concentration in influent and effluent and stable removal efficiency.</p>
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<p>The sludge characteristics in the reactor: (<b>a</b>) MLVSS and MLSS; (<b>b</b>) SVI and MLVSS/MLSS; (<b>c</b>) <span class="html-italic">d<sub>50</sub></span> and bacteria counts in the reactor.</p>
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<p>(<b>a</b>) Venn diagram showing unique and shared operational taxonomic units (OTUs) among the three sampling sites. (<b>b</b>) Principal component analysis (PCA) of the samples and (<b>c</b>) the OTUs number shift detected from samples.</p>
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<p>(<b>a</b>) Taxonomic classification of the bacterial communities in the GDMBR at genus levels; and (<b>b</b>) cluster analysis at genus levels.</p>
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<p>(<b>a</b>) Circos sample–species diagram; and (<b>b</b>) single-factor species correlation network heat map analysis.</p>
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<p>(<b>a</b>) Circos sample–species diagram; and (<b>b</b>) single-factor species correlation network heat map analysis.</p>
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12 pages, 4414 KiB  
Communication
Homogalacturonans and Hemicelluloses in the External Glands of Utricularia dichotoma Traps
by Bartosz J. Płachno, Małgorzata Kapusta, Marcin Feldo and Piotr Świątek
Int. J. Mol. Sci. 2024, 25(23), 13124; https://doi.org/10.3390/ijms252313124 - 6 Dec 2024
Viewed by 498
Abstract
The Utricularia (bladderworts) species are carnivorous plants that prey mainly on invertebrates using traps (bladders) of leaf origin. On the outer surfaces of the trap, there are dome-shaped glands (capitate trichomes). Each such trichome consists of a basal cell, a pedestal cell, and [...] Read more.
The Utricularia (bladderworts) species are carnivorous plants that prey mainly on invertebrates using traps (bladders) of leaf origin. On the outer surfaces of the trap, there are dome-shaped glands (capitate trichomes). Each such trichome consists of a basal cell, a pedestal cell, and a terminal cell. During the maturation of these external glands, there are changes in the cell wall of the terminal cell of the gland (deposited layers of secondary wall material). Thus, due to changes in the cell wall, these glands are excellent models for studying the specialization of cell walls. The main aim of this study was to check whether different cell wall layers in terminal gland cells have a different composition in the case of homogalacturonans (low-methylesterified HGs, fully de-esterified HGs, and galactan) and hemicelluloses (galactoxyloglucan, xyloglucan, and xylan). The antibodies were used against cell wall components (anti-pectins JIM5, JIM7, LM19, CCRC-M38, and LM5 and anti-hemicelluloses LM25, LM15, CCRC-M1, and CCRC-M138). The localization of the examined compounds was determined using immunohistochemistry techniques, Carbotrace 680, and Calcofluor White. Our study showed the presence of various components in the cell walls of external gland cells: methylesterified and demethylesterified homogalacturonans, galactan, xylan, galactoxyloglucan, and xyloglucan. In the terminal cell, the primary cell wall contains different pectins in contrast to the secondary wall material, which is rich in cellulose and hemicelluloses. We also found that the basal cell differs from the other gland cells by the presence of galactan in the cell wall, which resembles the epidermal cells and parenchyma of traps. A particularly noteworthy part of the cell wall functions as a Casparian strip in the pedestal cell. Here, we found no labeling with Carbotrace 680, possibly due to cell wall modification or cell wall chemical composition variation. We have shown that the apoplastic space formed by the cell walls of the terminal cell is mainly composed of cellulose and hemicelluloses (galactoxyloglucan and xyloglucan). This composition of the cell walls allows the easy uptake of components from the external environment. Our research supports the external glands’ function as hydropotens. Full article
(This article belongs to the Special Issue Latest Research on Plant Cell Wall)
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<p>External gland distribution and structure. (<b>A</b>) Trap epidermis with external glands (arrows), treated with toluidine blue; the glands absorbed the dye; the bar is 100 µm. (<b>B</b>) The structure of the external gland, terminal cell (Tc), pedestal cell (Pc), and basal cell (Bc); the bar is 10 µm.</p>
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<p>Homogalacturonan distribution in the external gland (intense green color—signal of antibody, blue color—cellulose stained by Calcofluor White), terminal cell (Tc), pedestal cell (Pc), and basal cell (Bc). (<b>A</b>) A section through the external gland, labeled with JIM5; the bar is 10 µm. (<b>B</b>) The same section as in A, labeled with JIM5 and Calcofluor White; the bar is 10 µm. (<b>C</b>) A section through the external gland, labeled with JIM5; the bar is 10 µm. (<b>D</b>) A section through the external gland, labeled with LM19; the bar is 10 µm. (<b>E</b>) The same section as in (<b>D</b>), labeled with LM19 and Calcofluor White; the bar is 10 µm. (<b>F</b>) A section through the external gland, labeled with LM19; the bar is 10 µm. (<b>G</b>) A section through the external gland, labeled with CCRC-M38; the bar is 10 µm. (<b>H</b>) The same section as in (<b>G</b>), labeled with CCRC-M38 and Calcofluor White; the bar is 10 µm. (<b>I</b>) A section through the external gland, labeled with CCRC-M38; the bar is 10 µm.</p>
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<p>Homogalacturonan distribution in the external gland (intense green color—signal of antibody, blue color—cellulose stained by Calcofluor White), terminal cell (Tc), pedestal cell (Pc), and basal cell (Bc). (<b>A</b>) A section through the external gland, labeled with JIM7; the bar is 10 µm. (<b>B</b>) A section through the external gland, labeled with LM5; the bar is 10 µm. (<b>C</b>) A section through the external gland, labeled with LM5; the bar is 10 µm. (<b>D</b>) The same section as in (<b>C</b>), labeled with LM5 and Calcofluor White; the bar is 10 µm.</p>
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<p>Hemicellulose (xyloglucan) distribution in the external gland (intense green color—signal of antibody, blue color—cellulose stained by Calcofluor White), terminal cell (Tc), pedestal cell (Pc), and basal cell (Bc). (<b>A</b>) A section through the external gland, labeled with CCRC-M138; the bar is 10 µm. (<b>B</b>) The same section as in A, labeled with CCRC-M138 and Calcofluor White; the bar is 10 µm. (<b>C</b>) A section through the external gland, labeled with CCRC-M138; the bar is 10 µm. (<b>D</b>) A section through the external gland, labeled with CCRC-M1; the bar is 10 µm. (<b>E</b>,<b>F</b>) A section through the external gland and through the terminal cell, labeled with LM15; the bar is 10 µm.</p>
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<p>Hemicellulose (galactoxyloglucan) distribution in the external gland (intense green color—signal of antibody, blue color—cellulose stained by Calcofluor White), terminal cell (Tc), pedestal cell (Pc), and basal cell (Bc). (<b>A</b>) A section through the external gland, labeled with LM25; the bar is 10 µm. (<b>B</b>) The same section as in A, labeled with LM25 and Calcofluor White; the bar is 10 µm. (<b>C</b>) A section through the external gland, labeled with LM25, noting the cell wall ingrowths in the pedestal cell (arrow); the bar is 10 µm. (<b>D</b>) A section through the external gland, labeled with LM25; the bar is 10 µm.</p>
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<p>Dye staining the external gland, terminal cell (Tc), pedestal cell (Pc), and basal cell (Bc). (<b>A</b>,<b>B</b>) A section through the external gland stained by Carbotrace 680 (red color); the bar is 10 µm. (<b>C</b>) A section through the external gland stained by Calcofluor White (blue color); the bar is 10 µm.</p>
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16 pages, 3359 KiB  
Article
Integrated System of Reverse Osmosis and Forward Pressure-Assisted Osmosis from ZrO2 Base Polymer Membranes for Desalination Technology
by Saleh O. Alaswad, Heba Abdallah and Eman S. Mansor
Technologies 2024, 12(12), 253; https://doi.org/10.3390/technologies12120253 - 6 Dec 2024
Viewed by 544
Abstract
In this work, reverse osmosis and forward osmosis membranes were prepared using base cellulosic polymers with ZrO2. The prepared membranes were rolled on the spiral-wound configuration module. The modules were tested on a pilot unit to investigate the efficiency of the [...] Read more.
In this work, reverse osmosis and forward osmosis membranes were prepared using base cellulosic polymers with ZrO2. The prepared membranes were rolled on the spiral-wound configuration module. The modules were tested on a pilot unit to investigate the efficiency of the RO membrane and the hydraulic pressure effect on both sides of the FO membranes. The RO membrane provided a rejection of 99% for the seawater desalination, and the brine was used as a draw solution for the FO system. First, seawater was used as a draw solution to indicate the best hydraulic pressure, where the best one was 3 bar for the draw solution side, and 2 bar for the feed side, where the water flux reached 48.89 L/m2·h (LMH) with a dilution percentage of 80% and a low salt reverse flux of 0.128 g/m2·h (gMH) after 5 h of operation time. The integrated system of RO and forward-assisted osmosis (PAO) was investigated using river water as a feed and RO brine as a draw solute, where the results of PAO indicate a high-water flux of 68.6 LMH with a dilution of 93.2% and a salt reverse flux of 0.18 gMH. Therefore, using PAO improves the performance of the system. Full article
(This article belongs to the Section Innovations in Materials Processing)
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<p>Machines for (<b>a</b>) casting large-scale membranes and (<b>b</b>) spiral-wound fabrication.</p>
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<p>Fabricated spiral-wound modules, (<b>a</b>) before fiberglass winding; (<b>b</b>) RO module and (<b>c</b>) FO module.</p>
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<p>Pilot testing unit for RO/FO modules.</p>
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<p>SEM images for (<b>a</b>) TEM for ZrO<sub>2</sub>, (<b>b</b>) RO blend membrane and (<b>c</b>) FO blend membrane.</p>
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<p>Effect of feeding saline concentration on (<b>a</b>) permeate flux and (<b>b</b>) salt rejection of prepared RO module.</p>
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<p>Effect of feeding saline concentration on (<b>a</b>) recovery of the prepared RO module, and (<b>b</b>) transmembrane pressure.</p>
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<p>Effect of pressure on the draw solute concentration and dilution percentage of draw solute. (<b>a</b>) Pressure of the DS of 1 bar to feed pressure of 2 bar; (<b>b</b>) pressure of the DS of 3 bar to feed pressure of 2 bar; (<b>c</b>) pressure of the DS of 2 bar to feed pressure of 2 bar.</p>
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<p>Effect of pressure on the draw solute to the pressure of the feed water on the salt flux and water flux. (<b>a</b>) Pressure of DS of 1 bar to feed pressure of 2 bar; (<b>b</b>) pressure of the DS of 3 bar to feed pressure of 2 bar; (<b>c</b>) pressure of the DS of 2 bar to feed pressure of 2 bar.</p>
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<p>Effect of DS pressure to feed pressure on the water flux and dilution %.</p>
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<p>Performance of FAO (<b>a</b>) using brine from RO as draw solution in terms of dilution % and TDS of draw solute; (<b>b</b>) water flux and salt reverse flux.</p>
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<p>Performance of FAO (<b>a</b>) using brine from RO as draw solution in terms of dilution % and TDS of draw solute; (<b>b</b>) water flux and salt reverse flux.</p>
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12 pages, 4539 KiB  
Article
A Flexible Sensing Material with High Force and Thermal Sensitivity Based on GaInSn in Capillary Embedded in PDMS
by Fandou Bao, Fengyao Ni, Qianqian Zhai, Zhizhuang Sun, Xiaolin Song and Yu Lin
Polymers 2024, 16(23), 3426; https://doi.org/10.3390/polym16233426 - 5 Dec 2024
Viewed by 578
Abstract
Flexible sensing materials have become a hot topic due to their sensitive electrical response to external force or temperature and their promising applications in flexible wear and human–machine interaction. In this study, a PDMS/capillary GaInSn flexible sensing material with high force and thermal [...] Read more.
Flexible sensing materials have become a hot topic due to their sensitive electrical response to external force or temperature and their promising applications in flexible wear and human–machine interaction. In this study, a PDMS/capillary GaInSn flexible sensing material with high force and thermal sensitivity was prepared utilizing liquid metal (LM, GaInSn), flexible silicone capillary, and polydimethylsiloxane (PDMS). The resistance (R) of the flexible sensing materials under the action of different forces and temperatures was recorded in real-time. The electrical performance results confirmed that the R of the sensing material was responsive to temperature changes and increased with the increasing temperature, indicating its ability to transmit temperature signals into electrical signals. The R was also sensitive to the external force, such as cyclic stretching, cyclic compression, cyclic bending, impact and rolling. The ΔR/R0 changed periodically and stably with the cyclic stretching, cyclic compression and cyclic bending when the conductive pathway diameter was 0.5–1.0 mm, the cyclic tensile strain ≤ 20%, the cyclic tensile rate ≤ 2.0 mm/min, the compression ratio ≤ 0.5, and the relative bending curvature ≤ 0.16. Moreover, the material exhibited sensitivity in detecting biological signals, such as the joint movements of the finger, wrist, elbow and the stand up-crouch motion. In conclusion, this work provides a method for preparing a sensing material with the capillary structure, which was confirmed to be sensitive to force and heat, and it produced different types of R signals under different deformations and different temperatures. Full article
(This article belongs to the Section Smart and Functional Polymers)
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<p>Model diagram of the PDMS/capillary GaInSn flexible sensing material.</p>
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<p>Δ<span class="html-italic">R/R</span><sub>0</sub> of the PDMS/capillary GaInSn flexible sensing material at different heating rates with the conductive path diameters of (<b>a</b>) 0.5 mm, (<b>b</b>) 0.8 mm, and (<b>c</b>) 1.0 mm. (<b>d</b>) Schematic diagram of the equipment connection for temperature sensitivity testing.</p>
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<p>Δ<span class="html-italic">R/R</span><sub>0</sub> of (<b>a</b>) the PDMS/capillary LM flexible sensing material and (<b>b</b>) the PDMS + PDMS/GaInSn + PDMS sensor materials under a specific heating procedure.</p>
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<p>(<b>a</b>) Diagram of the stretching equipment connection. (<b>b</b>) Correspondence of stress, strain, and Δ<span class="html-italic">R</span>/<span class="html-italic">R</span><sub>0</sub> under the cyclic stretching operations. The Δ<span class="html-italic">R</span>/<span class="html-italic">R</span><sub>0</sub> evolutions of the GaInSn flexible sensing material samples under cyclic stretching operations: (<b>c</b>) tensile strain 20%, tensile rate 2.0 mm/min, diameters 0.5/0.8/1.0 mm, (<b>d</b>) tensile strain 20%, diameter 0.5 mm, tensile rates of 1.0/1.5/2.0 mm/min, and (<b>e</b>) tensile rate 1.0 mm/min, diameter 0.5 mm, tensile strains 13.3%, 16.7%, and 20%.</p>
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<p>Δ<span class="html-italic">R</span>/<span class="html-italic">R</span><sub>0</sub> of the PDMS/capillary GaInSn sensing materials with different conductive path diameters of 0.5 mm, 0.8 mm, and 1.0 mm during (<b>a</b>) the compression process and (<b>b</b>) the bending process. (<b>c</b>) Actual operation pictures of the compression and bending.</p>
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<p>The brightness comparison of the bulb under the four conditions of the material in the (<b>a</b>) original, (<b>b</b>) stretched, (<b>c</b>) compressed, and (<b>d</b>) bent states.</p>
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<p>Δ<span class="html-italic">R/R</span><sub>0</sub> of the material under (<b>a</b>) impact operations and (<b>b</b>) rolling operations.</p>
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<p>Movement signals collection of the (<b>a</b>) elbow, (<b>b</b>) wrist, (<b>c</b>) finger and (<b>d</b>) the sole of foot.</p>
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