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Search Results (2,885)

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12 pages, 2224 KiB  
Article
A Spatial Analysis of Coffee Plant Temperature and Its Relationship with Water Potential and Stomatal Conductance Using a Thermal Camera Embedded in a Remotely Piloted Aircraft
by Luana Mendes dos Santos, Gabriel Araújo e Silva Ferraz, Milene Alves de Figueiredo Carvalho, Alisson André Vicente Campos, Pedro Menicucci Neto, Letícia Aparecida Gonçalves Xavier, Alessio Mattia, Valentina Becciolini and Giuseppe Rossi
Agronomy 2024, 14(10), 2414; https://doi.org/10.3390/agronomy14102414 (registering DOI) - 18 Oct 2024
Viewed by 188
Abstract
Coffee is a key agricultural product in national and international markets. Physiological parameters, such as plant growth indicators, can signal interruptions in these processes. This study aimed to characterize the temperature obtained by a thermal camera embedded in a remotely piloted aircraft (RPA) [...] Read more.
Coffee is a key agricultural product in national and international markets. Physiological parameters, such as plant growth indicators, can signal interruptions in these processes. This study aimed to characterize the temperature obtained by a thermal camera embedded in a remotely piloted aircraft (RPA) and evaluate its relationship with the water potential (WP) and stomatal conductance (gs) of an experimental coffee plantation using geostatistical techniques. The experiment was conducted at the Federal University of Lavras, Minas Gerais, Brazil. A rotary-wing RPA with an embedded thermal camera flew autonomously at a height of 10 m and speed of 10 m/s. Images were collected on 26 November 2019 (rainy season), and 11 August 2020 (dry season), between 9:30 am and 11:30 am. Data on gs and WP were collected in the field. The thermal images were processed using FLIR Tools 5.13, and temperature analysis and spatialization were undertaken using geostatistical tools and isocolor maps by Kriging interpolation in R 4.3.2 software. Field data were superimposed on final crop temperature maps using QuantumGIS version 3.10 software. The study found that with decreasing WP, stomatal closure and reduction in gs occurred, increasing the temperature due to water deficit. The temperature distribution maps identified areas of climatic variations indicating water deficit. Full article
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<p>Limit of the study area and location of the sampling points of each plot.</p>
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<p>Equipment: (<b>a</b>) RPA (Matrice 100) used for the survey with a thermal camera attached; (<b>b</b>) bottom view of the equipment detailing the camera; (<b>c</b>) the thermal camera, FLIR DUO (Inc., Boston, MA, USA); (<b>d</b>) an example of the control plates used in the study area.</p>
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<p>Graphical representation of the meteorological variables recorded monthly in Lavras, MG, from November 2019 to August 2020.</p>
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<p>Spatial distribution of the temperature and stomatal conductance (gs) of coffee plants in the (<b>a</b>) rainy season; (<b>b</b>) dry season.</p>
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<p>Spatial distribution of temperature and water potential (MPa) of coffee plants. (<b>a</b>) rainy season; (<b>b</b>) dry season.</p>
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<p>Regression and correlation between temperature and water potential (WP) and temperature and stomatal conductance (gs) of coffee plants in the rainy season and dry season.</p>
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12 pages, 1126 KiB  
Article
Enhancing Prostate Cancer Staging: Association of 68Ga-PSMA PET/CT Imaging with Histopathological Grading in Treatment-Naive Patients
by Oleksii Pisotskyi, Piotr Petrasz, Piotr Zorga, Marcin Gałęski, Pawel Szponar, Katarzyna Brzeźniakiewicz-Janus, Tomasz Drewa, Krzysztof Kaczmarek, Michał Cezary Czarnogórski and Jan Adamowicz
Cancers 2024, 16(20), 3526; https://doi.org/10.3390/cancers16203526 - 18 Oct 2024
Viewed by 195
Abstract
Objective: This study aimed to evaluate the correlation between 68Ga-PSMA uptake in PSMA PET/CT in primary prostate cancer (PC) and its histopathological grading (Gleason score and ISUP grade). Additionally, we compared preoperative biopsy histopathological findings with definitive pathology results in radical prostatectomy (RP) [...] Read more.
Objective: This study aimed to evaluate the correlation between 68Ga-PSMA uptake in PSMA PET/CT in primary prostate cancer (PC) and its histopathological grading (Gleason score and ISUP grade). Additionally, we compared preoperative biopsy histopathological findings with definitive pathology results in radical prostatectomy (RP) specimens. Methods: We retrospectively analyzed 86 patients who underwent 68Ga-PSMA PET/CT for primary PC staging, of which 40 patients later underwent radical prostatectomy. PET/CT results, including SUVmax values, were correlated with GS and PSA concentrations. Histopathology reports were analyzed and compared between biopsy and final pathology results following RP. Results: A significant positive correlation was observed between SUVmax and ISUP grades (Pearson’s ρ = 0.34, p < 0.001), with higher SUVmax values associated with more advanced grades. A cut-off SUVmax value of 5.64 was determined to predict upstaging in patients, yielding a sensitivity of 76% and a specificity of 60% (AUC = 0.82, 95% CI: 0.70–0.94). Additionally, 57.5% of patients experienced a grade shift following RP, with a 35% upgrade and 22.5% downgrade in ISUP grades. Conclusion: 68Ga-PSMA PET/CT demonstrated high sensitivity in detecting high-risk prostate cancer, particularly in patients with GS > 7 or PSA levels ≥ 10 ng/mL. The findings suggest that this imaging modality may be less effective for the staging of patients with lower GS or PSA values, that is, low-risk PCa. Further prospective studies are necessary to validate these results. Full article
(This article belongs to the Special Issue Advances in the Management of Pelvic Tumors)
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<p>Correlation between SUVmax and tumor grade group. This scatter plot illustrates the moderately positive correlation between SUVmax and tumor grade groups in a cohort of 86 prostate cancer patients. The red best fit line indicates the relationship between SUVmax and ISUP grade, with a Pearson’s correlation coefficient of ρ = 0.34, demonstrating statistical significance (<span class="html-italic">p</span> &lt; 0.001). This finding suggests that higher SUVmax values are associated with more advanced tumor grade groups.</p>
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<p>Correlation between SUVmax and PSA. This scatter plot shows a moderately positive correlation between PSA concentration levels and SUVmax values in prostate cancer patients. The best fit line, represented in red, demonstrates a Pearson’s correlation coefficient of ρ = 0.42, indicating a statistically significant relationship (<span class="html-italic">p</span> &lt; 0.001). This suggests that as PSA levels increase, SUVmax values tend to rise, reflecting a potential link between higher PSA concentrations and increased tumor metabolic activity.</p>
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<p>ROC Curve Analysis of SUVmax for Risk Stratification in Prostate Cancer. Following radical prostatectomy, 27.5% (<span class="html-italic">n</span> = 11) of patients were upstaged from low-risk (grade groups 1 + 2) to high-risk levels (grade groups 3 + 4 + 5), while 7.5% (<span class="html-italic">n</span> = 3) moved from high-risk to low-risk levels. An SUVmax cut-off of 5.64 was seen in 4 out of 1l patients (36.36%) who transitioned to higher-risk groups. The ROC curve analysis of SUVmax. (AUC = 0.82, 95% Cl: 0.70–0.94) demonstrated a sensitivity of 76% and a specificity of 60% at the cut-off value of 5.64, suggesting a possible but limited role in predicting risk transitions.</p>
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13 pages, 1012 KiB  
Article
Lightweight Optic Disc and Optic Cup Segmentation Based on MobileNetv3 Convolutional Neural Network
by Yuanqiong Chen, Zhijie Liu, Yujia Meng and Jianfeng Li
Biomimetics 2024, 9(10), 637; https://doi.org/10.3390/biomimetics9100637 - 18 Oct 2024
Viewed by 247
Abstract
Glaucoma represents a significant global contributor to blindness. Accurately segmenting the optic disc (OD) and optic cup (OC) to obtain precise CDR is essential for effective screening. However, existing convolutional neural network (CNN)-based segmentation techniques are often limited by high computational demands and [...] Read more.
Glaucoma represents a significant global contributor to blindness. Accurately segmenting the optic disc (OD) and optic cup (OC) to obtain precise CDR is essential for effective screening. However, existing convolutional neural network (CNN)-based segmentation techniques are often limited by high computational demands and long inference times. This paper proposes an efficient end-to-end method for OD and OC segmentation, utilizing the lightweight MobileNetv3 network as the core feature-extraction module. Our approach combines boundary branches with adversarial learning, to achieve multi-label segmentation of the OD and OC. We validated our proposed approach across three public available datasets: Drishti-GS, RIM-ONE-r3, and REFUGE. The outcomes reveal that the Dice coefficients for the segmentation of OD and OC within these datasets are 0.974/0.900, 0.966/0.875, and 0.962/0.880, respectively. Additionally, our method substantially lowers computational complexity and inference time, thereby enabling efficient and precise segmentation of the optic disc and optic cup. Full article
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<p>Overview of the MBG-Net network architecture: (<b>a</b>) is the feature-extraction module; (<b>b</b>) is the boundary branch; (<b>c</b>) is the mask branch.</p>
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<p>An overview of discriminator network architecture.</p>
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<p>The sample images and corresponding annotation images of the Drishti-GS, RIM-ONE-r3, and REFUGE datasets are presented as follows: (<b>a</b>,<b>d</b>) represent the sample images and corresponding annotations of the Drishti-GS dataset; (<b>b</b>,<b>e</b>) are the RIM-ONE-r3 dataset sample map and the corresponding annotation map; (<b>c</b>,<b>f</b>) are the REFUGE dataset sample map and the corresponding annotation map.</p>
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<p>Prediction results of the Drishti-GS dataset (Image is the fundus picture, Ground Truth is the annotation map, and Prediction is the network prediction map).</p>
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<p>Prediction results of the RIM-ONE-r3 dataset (Image is the fundus picture, Ground Truth is the label map, and Prediction is the network prediction map).</p>
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<p>Prediction results of the REFUGE-train dataset (Image is the fundus picture, Ground Truth is the annotation map, and Prediction is the network prediction map).</p>
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<p>ROC curve and AUC evaluation results of different datasets on BGA-Net.</p>
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<p>Comparison of qualitative segmentation results under different module combinations: (<b>a</b>) the ROI area of the fundus image; (<b>b</b>) the manual annotation map; (<b>c</b>) the predicted segmentation map associated with the baseline model; (<b>d</b>) the predicted segmentation map for baseline + boundary branch; and (<b>e</b>) the predicted segmentation map for baseline + boundary branch + discriminator network (MBG-Net).</p>
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27 pages, 5002 KiB  
Article
The Diversity of Methylation Patterns in Serous Borderline Ovarian Tumors and Serous Ovarian Carcinomas
by Laura A. Szafron, Roksana Iwanicka-Nowicka, Piotr Sobiczewski, Marta Koblowska, Agnieszka Dansonka-Mieszkowska, Jolanta Kupryjanczyk and Lukasz M. Szafron
Cancers 2024, 16(20), 3524; https://doi.org/10.3390/cancers16203524 - 18 Oct 2024
Viewed by 207
Abstract
Background: Changes in DNA methylation patterns are a pivotal mechanism of carcinogenesis. In some tumors, aberrant methylation precedes genetic changes, while gene expression may be more frequently modified due to methylation alterations than by mutations. Methods: Herein, 128 serous ovarian tumors [...] Read more.
Background: Changes in DNA methylation patterns are a pivotal mechanism of carcinogenesis. In some tumors, aberrant methylation precedes genetic changes, while gene expression may be more frequently modified due to methylation alterations than by mutations. Methods: Herein, 128 serous ovarian tumors were analyzed, including borderline ovarian tumors (BOTS) with (BOT.V600E) and without (BOT) the BRAF V600E mutation, low-grade (lg), and high-grade (hg) ovarian cancers (OvCa). The methylome of the samples was profiled with Infinium MethylationEPIC microarrays. Results: The biggest number of differentially methylated (DM) CpGs and regions (DMRs) was found between lgOvCa and hgOvCa. By contrast, the BOT.V600E tumors had the lowest number of DM CpGs and DMRs compared to all other groups and, in relation to BOT, their genome was strongly downmethylated. Remarkably, the ten most significant DMRs, discriminating BOT from lgOvCa, encompassed the MHC region on chromosome 6. We also identified hundreds of DMRs, being of potential use as predictive biomarkers in BOTS and hgOvCa. DMRs with the best discriminative capabilities overlapped the following genes: BAIAP3, IL34, WNT10A, NEU1, SLC44A4, and HMOX1, TCN2, PES1, RP1-56J10.8, ABR, NCAM1, RP11-629G13.1, AC006372.4, NPTXR in BOTS and hgOvCa, respectively. Conclusions: The global genome-wide hypomethylation positively correlates with the increasing aggressiveness of ovarian tumors. We also assume that the immune system may play a pivotal role in the transition from BOTS to lgOvCa. Given that the BOT.V600E tumors had the lowest number of DM CpGs and DMRs compared to all other groups, when methylome is considered, such tumors might be placed in-between BOT and OvCa. Full article
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<p>Violin plots of methylation changes (average beta values) in the promoter and first-exon regions of the <span class="html-italic">TP53</span>, <span class="html-italic">MDM2</span>, and <span class="html-italic">CDKN1A</span> genes (the remaining significant results are presented in <a href="#app1-cancers-16-03524" class="html-app">Supplementary Figure S3</a>). The values range from 0 to 1 (where 0 means no methylation and 1 denotes 100% methylation of CpGs detected in the region). Each analysis is supplemented with the results of two non-parametric statistical tests: the Kruskal–Wallis test (to determine overall methylation differences between the groups) and the Wilcoxon rank sum test to identify differences between particular groups; NS—non-significant result. Low p-values are displayed in exponential notation (e–n), in which e (exponent) multiplies the preceding number by 10 to the minus nth power.</p>
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<p>Differentially methylated CpGs. (<b>A</b>): the upset plot demonstrating the number of differentially methylated CpGs in each inter-tumor-group comparison (blue bars) and the number of such CpGs (red bars) for the specific intersection of tumor groups (all sets included in the given intersection are indicated with black dots, that are connected with a line if the intersection contains more than one set). (<b>B</b>–<b>G</b>): the distribution of M-values for the most differentiating CpGs for each inter-tumor-group comparison, followed by genomic locations and gene names with strand identificators shown in brackets. M-value is the log2 of the ratio between signal intensities for probes specific to methylated (numerator) and unmethylated (denominator) cytosines in the given CpG site. The higher the M-value, the higher the methylation level.</p>
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<p>Context plots depicting the most significant DMR for each inter-tumor-group comparison. Each plot title contains encompassed gene name(s) with the DNA strand identifier (+/−), on which the coding sequence of each gene is located. Below, a chromosome ideogram, graphical representation of the genomic range, and DMR location within the genome are shown. These are followed by a line + dot plot demonstrating the distribution of beta values for each CpG and sample (dot) along with mean values for each CpG (line). The visualization of Dnase I hypersensitive sites (DHSS) and transcription factor binding sites (TFBS) is also provided for the assessment of transcriptional activity in each DMR. (<b>A</b>): BOT vs. BOT.V600E (chr11:g.both 47269539–47270908); (<b>B</b>): BOT vs. lgOvCa (chr6:g.both 32935236–32943025); (<b>C</b>): BOT vs. hgOvCa (chr2:g.both 63275602–63285097); (<b>D</b>): BOT.V600E vs. lgOvCa (chr6:g.both 30651511–30654559); (<b>E</b>): BOT.V600E vs. hgOvCa (chr1:g. 2221807–2222674); (<b>F</b>): lgOvCa vs. hgOvCa (chr10:g.both 134977981–134981930).</p>
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<p>Nominated regression analyses for selected DMRs in hgOvCa. (<b>A</b>–<b>F</b>): Cox regression analysis (OS) in the subgroup of tumors with TP53 accumulation for the <span class="html-italic">HMOX1(+)/NA(−)</span> genes. (<b>A</b>,<b>B</b>): AUC plot for uni- and multivariable models obtained before (<b>A</b>) and after (<b>B</b>) a bootstrap-based cross-validation of the original data set. A red dashed line in B indicates the same time point which was used to draw the time-dependent ROC curve (<b>C</b>). An optimal cutoff point for this ROC curve, was calculated based on the multivariable model using the Youden index. Discrimination sensitivity and specificity values for this cutoff point are also provided. (<b>D</b>): Kaplan-Meier survival curves obtained for the patients divided into two categories (risk higher (high) or lower (low) than for the ROC curve (<b>C</b>)-estimated cutoff point) based on the risk of death, calculated using the multivariable model. The Kaplan-Meier curves are supplemented with the result of the log-rank test, as well. Box (<b>E</b>) and bar (<b>F</b>) plots depicting mean methylation beta values within the DMR in patients with the high or low risk of death. (<b>G</b>–<b>I</b>): logistic regression analysis (CR) for a DMR in unknown gene(s), in the subgroup of patients treated with the TP regimen. (<b>G</b>): ROC curves for uni- and multivariable logistic regression models. Box (<b>H</b>) and bar (<b>I</b>) plots depicting mean methylation beta values within the DMR in patients with (1) and without (0) CR. RT: residual tumor; TP: taxane/platinum chemotherapy; CR: complete remission. Low p-values are displayed in exponential notation (e−n), in which e (exponent) multiplies the preceding number by 10 to the minus nth power.</p>
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<p>A nominated logistic regression analysis for a DMR in the <span class="html-italic">BAIAP3(+)/NA(−)</span> gene in the whole group of BOTS patients (Full table). (<b>A</b>): ROC curves for uni- and multivariable logistic regression models; Box (<b>B</b>) and bar (<b>C</b>) plots depicting mean methylation beta values within the DMR in tumors with (Yes) and without (No) microinvasion/non-invasive implants.</p>
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19 pages, 15089 KiB  
Article
Genome-Scale Identification of Wild Soybean Serine/Arginine-Rich Protein Family Genes and Their Responses to Abiotic Stresses
by Yanping Wang, Xiaomei Wang, Rui Zhang, Tong Chen, Jialei Xiao, Qiang Li, Xiaodong Ding and Xiaohuan Sun
Int. J. Mol. Sci. 2024, 25(20), 11175; https://doi.org/10.3390/ijms252011175 - 17 Oct 2024
Viewed by 248
Abstract
Serine/arginine-rich (SR) proteins mostly function as splicing factors for pre-mRNA splicing in spliceosomes and play critical roles in plant development and adaptation to environments. However, detailed study about SR proteins in legume plants is still lacking. In this report, we performed a genome-wide [...] Read more.
Serine/arginine-rich (SR) proteins mostly function as splicing factors for pre-mRNA splicing in spliceosomes and play critical roles in plant development and adaptation to environments. However, detailed study about SR proteins in legume plants is still lacking. In this report, we performed a genome-wide investigation of SR protein genes in wild soybean (Glycine soja) and identified a total of 31 GsSR genes from the wild soybean genome. The analyses of chromosome location and synteny show that the GsSRs are unevenly distributed on 15 chromosomes and are mainly under the purifying selection. The GsSR proteins can be phylogenetically classified into six sub-families and are conserved in evolution. Prediction of protein phosphorylation sites indicates that GsSR proteins are highly phosphorylated proteins. The protein–protein interaction network implies that there exist numerous interactions between GsSR proteins. We experimentally confirmed their physical interactions with the representative SR proteins of spliceosome-associated components such as U1-70K or U2AF35 by yeast two-hybrid assays. In addition, we identified various stress-/hormone-responsive cis-acting elements in the promoter regions of these GsSR genes and verified their expression patterns by RT-qPCR analyses. The results show most GsSR genes are highly expressed in root and stem tissues and are responsive to salt and alkali stresses. Splicing analysis showed that the splicing patterns of GsSRs were in a tissue- and stress-dependent manner. Overall, these results will help us to further investigate the biological functions of leguminous plant SR proteins and shed new light on uncovering the regulatory mechanisms of plant SR proteins in growth, development, and stress responses. Full article
(This article belongs to the Special Issue Physiology and Molecular Biology of Plant Stress Tolerance)
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<p>Comparative phylogenetic tree of GsSR, AtSR, and OsSR proteins. The maximum likelihood (ML) tree was constructed based on the amino acid sequences of SR proteins from <span class="html-italic">Glycine soja</span>, <span class="html-italic">Arabidopsis thaliana,</span> and <span class="html-italic">Oryza sativa</span> using IQ-tree incorporated in TBtools with 5000 bootstrap replicates. The different colors indicate different sub-families.</p>
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<p>Chromosomal distribution and collinearity analysis of GsSR protein genes. (<b>A</b>) Chromosomal distribution of GsSR protein genes. The left scale determines the position of each <span class="html-italic">GsSR</span> on chromosome. Different shades of color reflect the distribution of gene density on chromosomes. (<b>B</b>) Inter-chromosomal relationships and segmental duplication of <span class="html-italic">GsSRs</span>. The green blocks indicate the part of wild soybean chromosomes (Chr01–Chr20). The duplicated GsSR protein gene pairs are highlighted in red lines. (<b>C</b>) Synteny analyses of SR protein genes between wild soybean and model plant species (Arabidopsis and rice). The gray lines indicate collinear blocks, and syntenic SR protein gene pairs are highlighted in blue lines.</p>
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<p>The gene structure and conserved protein motifs of 31 GsSR protein members. (<b>A</b>) The neighbor joining (NJ) tree was constructed using MEGA7 with 1000 bootstrap replicates. (<b>B</b>) Gene structure of GsSR protein genes. Grey boxes denote UTRs (untranslated regions); purple boxes denote exons; black lines denote introns. (<b>C</b>) Conserved motif analysis of GsSR proteins. A scale bar is provided at the bottom, and the length of each gene/protein is shown proportionally.</p>
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<p>Search of stress/hormone-associated <span class="html-italic">cis</span>-acting elements on <span class="html-italic">GsSR</span> gene promoters. (<b>A</b>) Putative stress/hormone-associated <span class="html-italic">cis</span>-acting elements in the promoter regions of <span class="html-italic">GsSR</span> genes. The putative <span class="html-italic">cis</span>-acting elements were searched from the 2000 bp promoter regions in the upstream of coding sequences of <span class="html-italic">GsSR</span> genes by using PlantCARE database. (<b>B</b>) Statistics of putative stress/hormone-associated <span class="html-italic">cis</span>-acting elements.</p>
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<p>Prediction of phosphorylation sites on GsSR proteins. (<b>A</b>) The distribution of phosphorylated serine (pSer), phosphorylated threonine (pThr), and phosphorylated tyrosine (pTyr) sites on GsSR proteins; (<b>B</b>) the sequence logos of the conserved motifs around the phosphosites (pSer or pTyr) extracted from GsSR proteins.</p>
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<p>Physical interactions between representative GsSR proteins and snRNPs revealed by Y2H assay. Yeast cells carrying the indicated constructs were diluted and grown on SD/-Trp-Leu or SD/-Trp-Leu-His medium for 6 days at 28 °C.</p>
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<p>Heatmap representation of expression profiles of the selected 20 <span class="html-italic">GsSR</span> genes in different tissues of wild soybean.</p>
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<p>Expression patterns of <span class="html-italic">GsSR</span> genes from wild soybean under salt and alkali stresses. (<b>A</b>) Expression patterns of selected 20 <span class="html-italic">GsSR</span> genes under salt treatment (150 mM NaCl) for 0, 3, 6 and 12 h respectively; (<b>B</b>) expression patterns of selected 10 <span class="html-italic">GsSR</span> genes under alkali treatment (150 mM NaHCO<sub>3</sub>) for 0, 3, 6, and 12 h, respectively. The error bars represent the standard error of the means of three replicates.</p>
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<p>Analyses of splicing patterns of selected eight <span class="html-italic">GsSR</span> genes based on RT-PCR. The diagrams on the left are schematic diagrams of predicted alternatively spliced transcripts of <span class="html-italic">GsSR6</span>, <span class="html-italic">GsSR11</span>, <span class="html-italic">Gs17</span>, and <span class="html-italic">GsSR29</span>. Green boxes represent exons, purple boxes represent untranslated regions (UTRs), and black lines represent introns. The red arrowheads indicate the position of primers used for RT-PCR. The numbers in the middle indicate the expected sizes of PCR products. The diagrams on the right are the representative gel images of RT-PCR results. The wild soybean seedlings were treated with salt (200 mM NaCl) or alkali (100 mM NaHCO<sub>3</sub>) for 6 h. R: root, L: leaf.</p>
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26 pages, 8121 KiB  
Article
Mixed Th1/Th2/Th17 Responses Induced by Plant Oil Adjuvant-Based B. bronchiseptica Vaccine in Mice, with Mechanisms Unraveled by RNA-Seq, 16S rRNA and Metabolomics
by Xuemei Cui, Qiuju Xiang, Yee Huang, Quanan Ji, Zizhe Hu, Tuanyuan Shi, Guolian Bao and Yan Liu
Vaccines 2024, 12(10), 1182; https://doi.org/10.3390/vaccines12101182 - 17 Oct 2024
Viewed by 293
Abstract
Background/Objectives: The current Bordetella bronchiseptica (Bb) vaccine, when adjuvanted with alum, does not elicit adequate robust cellular immunity or effective antibody defense against Bb attacks. Unfortunately, antibiotic treatment generally represents an ineffective strategy due to the development of resistance against a broad range [...] Read more.
Background/Objectives: The current Bordetella bronchiseptica (Bb) vaccine, when adjuvanted with alum, does not elicit adequate robust cellular immunity or effective antibody defense against Bb attacks. Unfortunately, antibiotic treatment generally represents an ineffective strategy due to the development of resistance against a broad range of antibiotics. Methods: The present study was designed to investigate the immune response, protective capabilities and underlying mechanisms of a plant oil-based adjuvant E515 formulated with inactivated Bb antigen as a potential vaccine candidate against Bordetella bronchiseptica. Results: Immunization studies revealed that a combination of SO, VE and GS (E515) exhibited a good synergistic adjuvant effect. The E515 adjuvanted Bb vaccine was proven to be highly efficacious and induced a mixed Th1/Th2/Th17 immune response in mice, leading to a significant increase in Bb-specific IgG, IgG1 and IgG2a antibodies, proliferative lymphocyte responses and cytokine levels (by lymphocytes and serum) and effectively induced responses by CD4+ TE, TM cells and B cells. The E515 adjuvant significantly enhanced the immune protection provided by the Bb vaccine in a mice model, as indicated by a reduced bacterial burden in the lungs. Multi-omics sequencing analysis revealed that E515 functions as an adjuvant by modulating critical pathways, including cytokine–cytokine receptor interaction, the IL-17 signaling pathway and the chemokine signaling pathway. This modulation also included interactions with beneficial species of bacteria including Alistipes, Odoribacter and Colidextribacter, as well as energy and lipid-related metabolites, thus highlighting its role as an immunomodulatory agent. Conclusion: Collectively, our results demonstrate the huge potential of E515-Bb vaccine candidates, thus highlighting the vegetable oil original adjuvant E515 as a promising agent for the development of new veterinary vaccines. Full article
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<p>Experimental design. (<b>A</b>) Synergistic effects of E515 adjuvant on Bb vaccine. Mice (n = 6/group) were immunized intramuscularly (i.m.) on days 0 and 14. Blood samples were collected 3 and 7 days after boost to measure Bb-specific IgG. (<b>B</b>) Immune effects of the E515-Bb vaccine. Mice (n = 15/group) were i.m. Blood samples were collected 7, 14, 21 and 28 days after boosting to measure Bb-specific IgG, IgG1 and IgG2a. On day 14, spleens were collected to measure lymphocyte proliferation, relative mRNA expression, T/B cell differentiation and cytokine production (spleen and serum). On day 28, spleens and cecal contents were collected for transcriptomic, 16S rRNA sequencing and untargeted metabolomics analyses. (<b>C</b>) Protection effect of E515-Bb vaccine. Mice (n = 9/group) were immunized i.m. on day 0. On day 28 post-boosting, mice were challenged with live Bb (5.2 × 10<sup>9</sup> CFU/mice); seven days later lungs were collected for bacterial burdens quantified.</p>
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<p>Vaccine-induced humoral immune response (Mice, n = 6/group). (<b>A</b>) Blood samples were collected 3 and 7 days after boost to measure Bb-specific IgG. (<b>B</b>) Serum samples were collected 7, 14, 21 and 28 days after boosting to measure Bb-specific IgG. (<b>C</b>) IgG1 and IgG2a were measured 14 days after the boost. Data shown as mean ± SE. Bars with different letters are statistically different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Vaccine-induced cellular immune response (Mice, n = 6/group). Splenocytes were isolated from spleens 14 days after the boost. (<b>A</b>) SI splenocytes were stimulated by Con A (10 µg/mL), LPS (10 µg/mL) or Bb antigen (20 µg/mL) for 48 h. (<b>B</b>) The expression of GATA-3, T-bet and ROR-γt mRNA splenocytes were stimulated by the Bb antigen (20 µg/mL) for 24 h. (<b>C</b>–<b>F</b>) The concentration of the IFN-γ, IL-6, TGF-β1 and IL-17 splenocytes were stimulated by the Bb antigen (20 µg/mL) for 72 h. Data shown as mean ± SE. Bars with different letters are statistically different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Cytokine production in serum (Mice, n = 5/group). Serum samples were collected 14 days after the boost and detected by a cytokine array. (<b>A</b>) Heat map of hierarchical clustering of cytokines in Bb vs. alum. (<b>B</b>) Heat map of hierarchical clustering of cytokines in Bb vs. E515. (<b>C</b>) Heat map of hierarchical clustering of cytokines in alum vs. E515. (<b>D</b>) KEGG pathway enrichment of cytokines in Bb vs. alum. (<b>E</b>) KEGG pathway enrichment of cytokines in Bb vs. E515. (<b>F</b>) KEGG pathway enrichment of cytokines in alum vs. E515. Red color on the heatmap indicates cytokines are upregulated and blue indicates cytokines are downregulated. Dot size on the KEGG pathway represents the number of cytokines; the color represents the <span class="html-italic">p</span> value.</p>
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<p>Bb-specific T cell and B cell responses in the spleen (Mice, n = 5/group). Splenocytes were isolated from the spleens 14 days after the boost, and analyzed by flow cytometry. (<b>A</b>,<b>B</b>) Frequencies and quantification of the CD4<sup>+</sup>, CD8<sup>+</sup> T cells and CD4<sup>+</sup>/CD8<sup>+</sup> ratio. (<b>C</b>,<b>D</b>) Frequencies and quantification of the CD4<sup>+</sup> TM (CD44<sup>+</sup> CD62L<sup>+</sup>) and TE (CD44<sup>+</sup> CD62L<sup>−</sup>) cells. (<b>E</b>,<b>F</b>) Frequencies and quantification of the CD8<sup>+</sup> TM and TE cells. (<b>G</b>,<b>H</b>) Frequencies and quantification of the plasmablasts (CD19<sup>+</sup> CD138<sup>+</sup> CD38<sup>+</sup>). (<b>I</b>,<b>J</b>) Frequencies and quantification of the plasma cells (CD19<sup>−</sup> CD138<sup>+</sup> CD38<sup>−</sup>). (<b>K</b>,<b>L</b>) Frequencies and quantification of the GC B cells (CD19<sup>+</sup> Fas<sup>+</sup> CD38<sup>−</sup>). Data shown as mean ± SE. Bars with different letters are statistically different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>KEGG pathways analysis (n = 3 /group). Comparison of DEGs KEGG modules between Bb-vs-alum (<b>A</b>), Bb-vs-E515 (<b>B</b>) and alum-vs-E515 (<b>C</b>).</p>
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<p>Effect of E515 on the diversity and composition of gut microbiota (n = 6/group). (<b>A</b>) Rank–abundance curve. (<b>B</b>,<b>G</b>–<b>I</b>) β-diversity was detected using PCoA (principal coordinates analysis) and ANOSIM (non-metric multi-dimensional scaling). (<b>C</b>) Observed OTUs (operational taxonomic units). (<b>D</b>–<b>F</b>) α-Diversity was detected using Chao1, Shannon and Simpson indices. (<b>J</b>–<b>L</b>) Composition of gut microbiota was analyzed at the phylum, family and genus levels.</p>
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<p>Differences in microbial abundances were identified by linear discriminant analysis (LDA, LDA score &gt; 2) and linear discriminant analysis effect size (LEfSe) analyses. (<b>A</b>) Bb-vs-E515. (<b>B</b>) alum-vs-E515.</p>
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<p>KEGG pathway analysis of differential microbes in the three groups.</p>
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<p>Effect of E515 on the changes of gut metabolic (n = 6 /group). (<b>A</b>) PLS-DA analysis score plots of the metabolic profiles in the negative ion mode. (<b>B</b>) PLS-DA analysis score plots of the metabolic profiles in the positive ion mode. PLS-DA and OPLS-DA analysis score plots of the metabolic profiles in the negative ion mode. Cross-validation results in the negative ion mode. (<b>C</b>) Differential expressed metabolites (DEMs) in every comparison group (VIP &gt; 1 and <span class="html-italic">p</span> &lt; 0.05). (<b>D</b>–<b>F</b>) KEGG pathway analysis of the differential metabolites in every comparison groups.</p>
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<p>Pearson’s correlation analysis among metabolites and microbes. (<b>A</b>) Bb-vs-E515. (<b>B</b>) Alum-vs-E515. Positive correlation marked with red color, negative correlation marked with green color, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Protective effect of E515-Bb vaccine on mice post-Bb challenge. Mice (n = 9/group) were s.c. injected with 0.2 mL of inactivated Bb antigen (3 × 10<sup>9</sup> CFU/mL) or Bb antigen adjuvanted with E515 or alum. Then, mice were challenged by an intraperitoneal injection of live Bb (5.2 × 10<sup>9</sup> CFU/mice). Seven days after attack, bacterial loads in lungs were quantified (n = 6). Data are presented as mean ± SE. Bars with different letters are statistically different (<span class="html-italic">p</span> &lt; 0.05).</p>
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18 pages, 11619 KiB  
Article
Investigation of Friction and Erosion Wear Properties of Titanium and Titanium Alloy Pipes
by Ting Mao, Zhiming Yu, Jing Yan, Yong Xu, Shibo Zhang and Lincai Peng
Materials 2024, 17(20), 5043; https://doi.org/10.3390/ma17205043 (registering DOI) - 15 Oct 2024
Viewed by 335
Abstract
Titanium alloys are applied in oil and gas development and transportation to improve conditions because of their high specific strength and corrosion resistance. However, the disadvantage of poor wear resistance has become an obstacle to developing titanium alloys. The friction and wear properties [...] Read more.
Titanium alloys are applied in oil and gas development and transportation to improve conditions because of their high specific strength and corrosion resistance. However, the disadvantage of poor wear resistance has become an obstacle to developing titanium alloys. The friction and wear properties of pure titanium TA3 and titanium alloy TA10 were tested under different loads and different friction forms using a reciprocating friction and wear tester. Moreover, the erosion resistance of pure titanium TA3 and titanium alloy TA10 was studied using a gas–solid erosion tester. The results show that the wear rate of TA3 and titanium alloy TA10 increases with increasing friction load. Under a load of 50 N, the mass losses of TA3 under dry friction and wet friction were 0.0013 g and 0.0045 g, respectively, while the mass losses of TA10 were 0.0033 g and 0.0046 g, respectively. While the load increased to 70 N, the mass loss of TA3 was even greater, reaching 0.0065 g, and the mass loss of TA10 was 0.0058 g. The wear forms of TA3 and TA10 include abrasive wear, adhesive wear and oxidation wear. The joint action of various friction forms leads to the loss of materials. Under the simulated working conditions, the erosion rates of TA3 and TA10 were 1.01 × 10−3 g/s and 0.94 × 10−3 g/s. The erosion mechanism is the same, including plowing, indentation and cracking. Full article
(This article belongs to the Section Corrosion)
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<p>Experimental setup; (<b>a</b>) multi-function friction and wear tester, (<b>b</b>) air jet erosion tester.</p>
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<p>Macroscopic morphology of TA3 and TA10 after friction and wear tests under different working conditions ((<b>a</b>): 1#, (<b>b</b>): 2#, (<b>c</b>): 3#, (<b>d</b>): 4#, (<b>e</b>): 5#, (<b>f</b>): 6#).</p>
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<p>Macroscopic morphology of TA3 and TA10 after gas–solid erosion test ((<b>a</b>): TA3 and (<b>b</b>): TA10).</p>
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<p>Friction factor of TA3 and TA10 wear specimens.</p>
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<p>The curve of friction factor with time.</p>
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<p>The curve of friction factor with time.</p>
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<p>Three stages of surface wear.</p>
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<p>Microscopic images of wear topography under different friction conditions.</p>
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<p>Observation of wear morphology by laser confocal microscope.</p>
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<p>Section profile of friction mark.</p>
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<p>Measurement of average wear width, average wear depth and profile area. (<b>a</b>) Measurement method of wear scar width and depth, (<b>b</b>) The cross-sectional area of the contour is measured by integral.</p>
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<p>Average wear width and average wear depth ((<b>a</b>): average wear width; (<b>b</b>): average wear depth).</p>
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<p>Wear mass and volume of samples.</p>
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<p>SEM images of wear topography under different friction conditions. (<b>a1</b>–<b>a3</b>) TA3 during 50 N wet friction, (<b>b1</b>–<b>b3</b>) TA3 during 50 N dry friction, (<b>c1</b>–<b>c3</b>) TA3 during 70 N dry friction, (<b>d1</b>–<b>d3</b>) TA10 during 50 N wet friction, (<b>e1</b>–<b>e3</b>) TA10 during 50 N dry friction, (<b>f1</b>–<b>f3</b>) TA10 during 70 N dry friction.</p>
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<p>3D surface profile of eroded samples ((<b>a1</b>–<b>c1</b>): TA3; (<b>a2</b>–<b>c2</b>): TA10).</p>
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<p>Erosion micromorphology of TA3 and TA10 ((<b>a</b>): TA3; (<b>b</b>): TA10).</p>
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<p>Formation and evolution of friction layer in friction and wear. (<b>a</b>) contact phase, (<b>b</b>) wear debris generation, (<b>c</b>) friction oxide formation, (<b>d</b>) generation of shedding zone.</p>
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27 pages, 15139 KiB  
Article
Nitrogen Level Impacts the Dynamic Changes in Nitrogen Metabolism, and Carbohydrate and Anthocyanin Biosynthesis Improves the Kernel Nutritional Quality of Purple Waxy Maize
by Wanjun Feng, Weiwei Xue, Zequn Zhao, Haoxue Wang, Zhaokang Shi, Weijie Wang, Baoguo Chen, Peng Qiu, Jianfu Xue and Min Sun
Plants 2024, 13(20), 2882; https://doi.org/10.3390/plants13202882 (registering DOI) - 15 Oct 2024
Viewed by 388
Abstract
Waxy corn is a special type of maize primarily consumed as a fresh vegetable by humans. Nitrogen (N) plays an essential role in regulating the growth progression, maturation, yield, and quality of waxy maize. A reasonable N application rate is vital for boosting [...] Read more.
Waxy corn is a special type of maize primarily consumed as a fresh vegetable by humans. Nitrogen (N) plays an essential role in regulating the growth progression, maturation, yield, and quality of waxy maize. A reasonable N application rate is vital for boosting the accumulation of both N and carbon (C) in the grains, thereby synergistically enhancing the grain quality. However, the impact of varying N levels on the dynamic changes in N metabolism, carbohydrate formation, and anthocyanin synthesis in purple waxy corn kernels, as well as the regulatory relationships among these processes, remains unclear. To explore the effects of varying N application rates on the N metabolism, carbohydrate formation, and anthocyanin synthesis in kernels during grain filling, a two-year field experiment was carried out using the purple waxy maize variety Jinnuo20 (JN20). This study examined the different N levels, specifically 0 (N0), 120 (N1), 240 (N2), and 360 (N3) kg N ha−1. The results of the analysis revealed that, for nearly all traits measured, the N application rate of N2 was the most suitable. Compared to the N0 treatment, the accumulation and content of anthocyanins, total nitrogen, soluble sugars, amylopectin, and C/N ratio in grains increased by an average of 35.62%, 11.49%, 12.84%, 23.74%, 13.00%, and 1.87% under N2 treatment over five filling stages within two years, respectively, while the harmful compound nitrite content only increased by an average of 30.2%. Correspondingly, the activities of related enzymes also significantly increased and were maintained under N2 treatment compared to N0 treatment. Regression and correlation analysis results revealed that the amount of anthocyanin accumulation was highly positively correlated with the activities of phenylalanine ammonia-lyase (PAL) and flavanone 3-hydroxylase (F3H), but negatively correlated with anthocyanidin synthase (ANS) and UDP-glycose: flavonoid-3-O-glycosyltransferase (UFGT) activity, nitrate reductase (NR), and glutamine synthetase (GS) showed significant positive correlations with the total nitrogen content and lysine content, and a significant negative correlation with nitrite, while soluble sugars were negatively with ADP-glucose pyrophosphorylase (AGPase) activity, and amylopectin content was positively correlated with the activities of soluble starch synthase (SSS), starch branching enzyme (SBE), and starch debranching enzyme (SDBE), respectively. Furthermore, there were positive or negative correlations among the detected traits. Hence, a reasonable N application rate improves purple waxy corn kernel nutritional quality by regulating N metabolism, as well as carbohydrate and anthocyanin biosynthesis. Full article
(This article belongs to the Topic Crop Ecophysiology: From Lab to Field, 2nd Volume)
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<p>Effects of N application doses on dynamic changes in anthocyanin accumulation amount (AAA) and content in grains of purple waxy maize at different days after pollination. (<b>a</b>) dynamic changes of the phenotypes of Jinnuo20 ears and kernels; (<b>b</b>) anthocyanin accumulation amount (AAA); (<b>c</b>) anthocyanin content (ANC). Different lowercase letters denote significant differences between N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Relationship between anthocyanin accumulation amount (AAA), anthocyanin content (ANC), and anthocyanin-biosynthesis-related enzymes in grains of purple waxy maize on different days after pollination. ** signify significant differences at the <span class="html-italic">p</span> &lt; 0.01 levels.</p>
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<p>Effects of N application doses on the dynamic changes in the kernel N content in grains of purple waxy maize on different days after pollination. Different lowercase letters denote significant differences between N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Effects of N application doses on dynamic changes in nitrite content (NC) in fresh grains of purple waxy maize at different days after pollination. Different lowercase letters denote significant differences between N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes a standard error based on 3 data.</p>
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<p>Effects of N application doses on the dynamic changes in lysine content (LC) in fresh grains of purple waxy maize at different days after pollination. Different lowercase letters denote significant differences between N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Effects of N application doses on dynamic changes in nitrate reductase (NR) and glutamine synthetase (GS) activities in fresh grains of purple waxy maize at different days after pollination. ns denotes no significant difference. Different lowercase letters denote significant differences between the N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Relationship between the total N content (TNC), nitrite content (NC) , and lysine content (LC) in fresh grains of purple waxy maize at different days after pollination. ** signify significant differences at <span class="html-italic">p</span> &lt; 0.01 levels.</p>
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<p>Effects of N application doses on dynamic changes of soluble sugar content (SSC) in fresh grains of purple waxy maize on different days after pollination. Different lowercase letters denote significant differences between the N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Effects of N application doses on dynamic changes in amylopectin content (AC) in the fresh grains of purple waxy maize on different days after pollination. Different lowercase letters denote significant differences between the N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes a standard error based on 3 data.</p>
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<p>Effects of the N rate on the enzymatic activity of carbon metabolism in fresh grains of purple waxy maize at different days after pollination. Different lowercase letters denote significant differences between N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Relationship between soluble sugar content (SSC), amylopectin content (AC) and the enzymatic activity of the carbon metabolism in fresh grains of purple waxy maize on different days after pollination. ** signify significant differences at the <span class="html-italic">p</span> &lt; 0.01 levels.</p>
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<p>Effects of the N rate on the grain C/N ratio in fresh grains of purple waxy maize on different days after pollination. Different lowercase letters denote significant differences between N rates at the <span class="html-italic">p</span> &lt; 0.05 level. The error bar denotes standard error based on 3 data.</p>
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<p>Correlation analysis of anthocyanin, N metabolism, and carbohydrate content of purple waxy maize. *, ** and *** denote significant differences at the <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">p</span> &lt; 0.01 and <span class="html-italic">p</span> &lt; 0.001 levels, respectively.</p>
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20 pages, 2521 KiB  
Article
Synergistic Effect of Arbuscular Mycorrhizal Fungi and Germanium on the Growth, Nutritional Quality, and Health-Promoting Activities of Spinacia oleracea L.
by Basma Najar, Ahlem Zrig, Emad A. Alsherif, Samy Selim, Abeer S. Aloufi, Shereen Magdy Korany, Mousa Nhs, Mohammad Aldilam and Nahla Alsayd Bouqellah
Plants 2024, 13(20), 2869; https://doi.org/10.3390/plants13202869 - 14 Oct 2024
Viewed by 398
Abstract
Arbuscular mycorrhizal fungi (AMF) and the antioxidant germanium (Ge) are promising tools for boosting bioactive compound synthesis and producing healthier foods. However, their combined effect remains unexplored. This study demonstrates the synergistic impact of AMF and Ge on the growth, metabolite accumulation, biological [...] Read more.
Arbuscular mycorrhizal fungi (AMF) and the antioxidant germanium (Ge) are promising tools for boosting bioactive compound synthesis and producing healthier foods. However, their combined effect remains unexplored. This study demonstrates the synergistic impact of AMF and Ge on the growth, metabolite accumulation, biological activities, and nutritional qualities of Spinacia oleracea L. (spinach), a globally significant leafy vegetable. Individually, Ge and AMF increased biomass by 68.1% and 22.7%, respectively, while their combined effect led to an 86.3% increase. AMF and Ge also improved proximate composition, with AMF–Ge interaction enhancing crude fiber and mineral content (p < 0.05). Interestingly, AMF enhanced photosynthesis-related parameters (e.g., total chlorophyll) in Ge treated plants, which in turn increased carbohydrate accumulation. This accumulation could provide a route for the biosynthesis of amino acids, organic acids, and fatty acids, as evidenced by increased essential amino acid and organic acid levels. Consistently, the activity of key enzymes involved in amino acids biosynthesis (e.g., glutamine synthase (GS), methionine biosynthase (MS), lysine biosynthase (LS)) showed significant increments. Furthermore, AMF improved fatty acid levels, particularly unsaturated fatty acids in Ge-treated plants compared to the control. In addition, increased phenylalanine provided a precursor for the production of antioxidants (e.g., phenols and flavonoids), through the action of the enzyme phenylalanine ammonia-lyase (PAL), resulting in improved antioxidant activity gains as indicated by FRAP, ABTS, and DPPH assays. This study is the first to show that Ge enhances the beneficial effect of AMF on spinach, improving growth and nutritional quality, with promising implications for agricultural practices. Full article
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<p>Effect of different treatments on biomass (<b>A</b>) and Ge level (<b>B</b>). Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on photosynthetic pigments, (<b>A</b>): chlorophyll a, chlorophyll b and chlorophyll ab; (<b>B</b>) b-carotene, lycopene. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on proximate composition, (<b>A</b>): moisture, (<b>B</b>): total protein, (<b>C</b>) crude fiber, (<b>D</b>): total lipd, (<b>E</b>): ash content, (<b>F</b>): carbohydrates. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on mineral contents, (<b>A</b>): Ca, FE and Mg; (<b>B</b>): Cu, Zn and Mn (<b>C</b>): K, Na and P. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on vitamin and sugar contents, (<b>A</b>): vitamin C, vitamin and L-galactose; (<b>B</b>): vitamin B1, vitamin B2 and D-mannose. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on antidiabetic activity. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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21 pages, 6056 KiB  
Article
Research on the Mechanism of Growth of Codonopsis pilosula (Franch.) Nannf. Root Responding to Phenolic Stress Induced by Benzoic Acid
by Yantong Ma, Lei Ma, Ling Xu, Ruonan Wei, Guiping Chen, Junhong Dang, Zhen Chen, Shaoying Ma and Sheng Li
Int. J. Mol. Sci. 2024, 25(20), 11007; https://doi.org/10.3390/ijms252011007 - 13 Oct 2024
Viewed by 489
Abstract
Soil autotoxic chemosensory substances have emerged as the predominant environmental factors constraining the growth, quality, and yield of Codonopsis pilosula in recent years. Among a vast array of chemosensory substances, benzoic acid constitutes the principal chemosensory substance in the successive cultivation of C. [...] Read more.
Soil autotoxic chemosensory substances have emerged as the predominant environmental factors constraining the growth, quality, and yield of Codonopsis pilosula in recent years. Among a vast array of chemosensory substances, benzoic acid constitutes the principal chemosensory substance in the successive cultivation of C. pilosula. However, the exploration regarding the stress exerted by benzoic acid on the growth and development of C. pilosula remains indistinct, and there is a scarcity of research on the mechanism of lobetyolin synthesis in C. pilosula. In the current research, it was discovered that exposure to benzoic acid at a concentration of 200 mmol/L conspicuously attenuated the plant height, root length, total length, fresh weight, root weight, root thickness, chlorophyll content, electrolyte osmolality, leaf intercellular CO2 concentration (Ci), net photosynthesis rate (Pn), transpiration rate (Tr), and leaf stomatal conductance (Gs) of C. pilosula. Benzoic acid (200 mmol/L) significantly enhanced the activity of root enzymes, including superoxide dismutase (SOD), malondialdehyde (MDA), and peroxidase (POD), as well as the accumulation of polysaccharides and lobetyolins (polyacetylene glycosides) in the roots of C. pilosula. In this study, 58,563 genes were assembled, and 7946 differentially expressed genes were discovered, including 4068 upregulated genes and 3878 downregulated genes. The outcomes of the histological examination demonstrated that benzoic acid stress augmented the upregulation of genes encoding key enzymes implicated in the citric acid cycle, fatty acid metabolism, as well as starch and sucrose metabolic pathways. The results of this investigation indicated that a moderate amount of benzoic acid could enhance the content of lobetyolin in C. pilosula and upregulate the expression of key coding genes within the signaling cascade to improve the resilience of C. pilosula lobetyolin against benzoic acid stress; this furnished a novel perspective for the study of C. pilosula lobetyolin as a potential substance for alleviating benzoic acid-induced stress. Full article
(This article belongs to the Section Molecular Plant Sciences)
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<p>Phenotypic manifestations of <span class="html-italic">C. pilosula</span> under diverse concentrations of benzoic acid treatments. The upper portion showcases the phenotypic traits of potted plants, whereas the lower portion delineates the root morphology of <span class="html-italic">C. pilosula</span>.</p>
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<p>Morphological parametric assessments of <span class="html-italic">C. pilosula</span> upon exposure to benzoic acid at a concentration of 200 mmol/L: (<b>A</b>) Plant height; (<b>B</b>) root length; (<b>C</b>) total plant length; (<b>D</b>) fresh weight; (<b>E</b>) root weight; (<b>F</b>) root thickness. Note: “*” indicates significant differences between treatments at (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Photosynthetic parameters under varying concentrations of benzoic acid treatments: (<b>A</b>) chlorophyll content; (<b>B</b>) leaf electrolyte osmolality; (<b>C</b>) Fv/Fm ratio; (<b>D</b>) leaf intercellular CO<sub>2</sub> concentration (Ci); (<b>E</b>) net photosynthetic rate (Pn); (<b>F</b>) leaf transpiration rate (Tr); (<b>G</b>) leaf stomatal conductance (Gs). Note: “*” indicates significant differences between treatments at (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Physiological and photosynthetic metrics under diverse concentrations of benzoic acid administration: (<b>A</b>) leaf superoxide dismutase activity; (<b>B</b>) leaf peroxidase activity; (<b>C</b>) leaf malondialdehyde content; (<b>D</b>) root superoxide dismutase activity; (<b>E</b>) root peroxidase activity; (<b>F</b>) root malondialdehyde content. Note: “*” signifies statistically noteworthy discrepancies between treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Expression profiling of genes associated with lobetyolin biosynthesis in the roots of <span class="html-italic">C. pilosula</span>: (<b>A</b>) Statistical charting of upregulated and downregulated genes in <span class="html-italic">C. pilosula</span> under control (CK) and benzoic acid (200 mmol/L) treatments; (<b>B</b>) shows a Venn plot depicting the cross expression of differentially expressed genes between CK and 200; Specifically, the two groups have a total of 20,209 genes, with 3174 and 3180 representing the genes uniquely expressed in each respective group; (<b>C</b>) fluctuations in lobetyolin content in the roots of <span class="html-italic">C. pilosula</span> under CK and benzoic acid (200 mmol/L) treatments; (<b>D</b>) modifications in polysaccharide content in the roots of <span class="html-italic">C. pilosula</span> under CK and benzoic acid (200 mmol/L) treatments. Note: “*” signifies statistically prominent disparities between treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Heatmap illustrating sample expression correlation: (<b>A</b>) The magnitude of each color block represents the correlation between two samples along the x and y axes; the higher the magnitude, the stronger the correlation. (<b>B</b>) Bubble plot demonstrating KEGG enrichment analysis of differentially expressed genes in <span class="html-italic">C. pilosula</span> upon CK and benzoic acid (200 mmol/L) treatment: The size of the bubbles reflects the count of enriched genes, with larger bubbles indicating a greater abundance of enriched genes, and the bubble colors signify the enrichment significance—darker colors correspond to higher q-values, <span class="html-italic">p</span> ≤ 0.01 and fold change ≥ 1.2. (<b>C</b>) Distinctive expression profiles of genes encoding key enzymes in the kynurenine synthesis pathway in <span class="html-italic">C. pilosula</span> roots subjected to CK and benzoic acid (200 mmol/L) treatments.</p>
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<p>Schematic illustration of the biosynthetic route for lobetyolin in <span class="html-italic">C. pilosula.</span> Dotted arrowhead indicates an indirect effect.</p>
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<p>FPKM trend profiling of enzyme-encoding genes relevant to the biosynthetic trajectory of lobetyolin in <span class="html-italic">C. pilosula</span>.</p>
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<p>Dynamic correlation heatmap annotation. Note: “*” designates significant disparities between treatments (<span class="html-italic">p</span> &lt; 0.05); “**” and “***” signify highly significant variances between treatments, (<span class="html-italic">p</span> &lt; 0.01) and (<span class="html-italic">p</span> &lt; 0.001) respectively.</p>
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<p>qRT-PCR analysis was conducted to examine the changes in DEGs in <span class="html-italic">C. pilosula</span> roots under CK and 200 mmol/L benzoic acid treatment. Nine DEGs that regulate key metabolic pathways were selected for qRT-PCR validation. The qRT-PCR values were compared with gene FPKM values to verify the reliability of transcriptomic data. “*” represents the results of Duncan’s multiple range test, indicating statistically significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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28 pages, 7076 KiB  
Article
Coupling Image-Fusion Techniques with Machine Learning to Enhance Dynamic Monitoring of Nitrogen Content in Winter Wheat from UAV Multi-Source
by Xinwei Li, Xiangxiang Su, Jun Li, Sumera Anwar, Xueqing Zhu, Qiang Ma, Wenhui Wang and Jikai Liu
Agriculture 2024, 14(10), 1797; https://doi.org/10.3390/agriculture14101797 - 12 Oct 2024
Viewed by 504
Abstract
Plant nitrogen concentration (PNC) is a key indicator reflecting the growth and development status of plants. The timely and accurate monitoring of plant PNC is of great significance for the refined management of crop nutrition in the field. The rapidly developing sensor technology [...] Read more.
Plant nitrogen concentration (PNC) is a key indicator reflecting the growth and development status of plants. The timely and accurate monitoring of plant PNC is of great significance for the refined management of crop nutrition in the field. The rapidly developing sensor technology provides a powerful means for monitoring crop PNC. Although RGB images have rich spatial information, they lack the spectral information of the red edge and near infrared bands, which are more sensitive to vegetation. Conversely, multispectral images offer superior spectral resolution but typically lag in spatial detail compared to RGB images. Therefore, the purpose of this study is to improve the accuracy and efficiency of crop PNC monitoring by combining the advantages of RGB images and multispectral images through image-fusion technology. This study was based on the booting, heading, and early-filling stages of winter wheat, synchronously acquiring UAV RGB and MS data, using Gram–Schmidt (GS) and principal component (PC) image-fusion methods to generate fused images and evaluate them with multiple image-quality indicators. Subsequently, models for predicting wheat PNC were constructed using machine-selection algorithms such as RF, GPR, and XGB. The results show that the RGB_B1 image contains richer image information and more image details compared to other bands. The GS image-fusion method is superior to the PC method, and the performance of fusing high-resolution RGB_B1 band images with MS images using the GS method is optimal. After image fusion, the correlation between vegetation indices (VIs) and wheat PNC has been enhanced to varying degrees in different growth periods, significantly enhancing the response ability of spectral information to wheat PNC. To comprehensively assess the potential of fused images in estimating wheat PNC, this study fully compared the performance of PNC models before and after fusion using machine learning algorithms such as Random Forest (RF), Gaussian Process Regression (GPR), and eXtreme Gradient Boosting (XGB). The results show that the model established by the fusion image has high stability and accuracy in a single growth period, multiple growth periods, different varieties, and different nitrogen treatments, making it significantly better than the MS image. The most significant enhancements were during the booting to early-filling stages, particularly with the RF algorithm, which achieved an 18.8% increase in R2, a 26.5% increase in RPD, and a 19.7% decrease in RMSE. This study provides an effective technical means for the dynamic monitoring of crop nutritional status and provides strong technical support for the precise management of crop nutrition. Full article
(This article belongs to the Section Digital Agriculture)
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Figure 1
<p>Chuzhou City, Anhui Province (<b>A</b>) and experiment design (<b>B</b>), with (<b>C</b>–<b>E</b>) representing the booting stage, heading stage, and early-filling stage, respectively.</p>
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<p>Image-fusion process flowchart. (<b>A</b>) represents the PC image-fusion method; (<b>B</b>) represents the GS image-fusion method.</p>
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<p>Flow chart in this study.</p>
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<p>Comprehensive strategy for model construction.</p>
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<p>Information entropy of RGB band images of wheat canopy. B1, B2, and B3 correspond to the red, green, and blue bands of the RGB imagery, respectively.</p>
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<p>Correlation change of band information and wheat PNC before and after image fusion.</p>
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<p>Correlation change of VIs and wheat PNC before and after image fusion.</p>
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<p>Compared to the MS model, the improvements of the fusion image model from the <span class="html-italic">R</span><sup>2</sup> perspective.</p>
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<p>Compared to the MS model, the improvements of the fusion image model from the <span class="html-italic">RMSE</span> and <span class="html-italic">RPD</span> perspective.</p>
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<p>Estimating PNC across different varieties. V1, V2, and V3 represent Huaimai 44, Yannong 999, and Ningmai 13, respectively.</p>
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<p>Estimating PNC across different nitrogen treatments. N0, N1, N2, and N3 represent 0 kg/ha, 100 kg/ha, 200 kg/ha, and 300 kg/ha, respectively.</p>
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<p>The importance and interaction of variables within the model. Vint represents variable interactions, and Vimp represents variable importance.</p>
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<p>Winter wheat PNC spatiotemporal distribution map. (<b>a</b>) represents the measured PNC, and (<b>b</b>) represents the predicted PNC.</p>
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<p>The RF algorithm’s Vint and Vimp from 100 cycles of sampling for both fusion and MS images during the heading stage. Vint represents variable interactions, and Vimp represents variable importance.</p>
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<p>Difference treatment on the correlation (|r|) between feature variables in the fusion image and MS image.</p>
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28 pages, 3798 KiB  
Article
Smooth Sigmoid Surrogate (SSS): An Alternative to Greedy Search in Decision Trees
by Xiaogang Su, George Ekow Quaye, Yishu Wei, Joseph Kang, Lei Liu, Qiong Yang, Juanjuan Fan and Richard A. Levine
Mathematics 2024, 12(20), 3190; https://doi.org/10.3390/math12203190 - 11 Oct 2024
Viewed by 581
Abstract
Greedy search (GS) or exhaustive search plays a crucial role in decision trees and their various extensions. We introduce an alternative splitting method called smooth sigmoid surrogate (SSS) in which the indicator threshold function used in GS is approximated by a smooth sigmoid [...] Read more.
Greedy search (GS) or exhaustive search plays a crucial role in decision trees and their various extensions. We introduce an alternative splitting method called smooth sigmoid surrogate (SSS) in which the indicator threshold function used in GS is approximated by a smooth sigmoid function. This approach allows for parametric smoothing or regularization of the erratic and discrete GS process, making it more effective in identifying the true cutoff point, particularly in the presence of weak signals, as well as less prone to the inherent end-cut preference problem. Additionally, SSS provides a convenient means of evaluating the best split by referencing a parametric nonlinear model. Moreover, in many variants of recursive partitioning, SSS can be reformulated as a one-dimensional smooth optimization problem, rendering it computationally more efficient than GS. Extensive simulation studies and real data examples are provided to evaluate and demonstrate its effectiveness. Full article
(This article belongs to the Special Issue Statistics and Data Science)
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Figure 1
<p>Plot of the goodness-of-split measure <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mo>????</mo> <mo>(</mo> <mi>c</mi> <mo>)</mo> </mrow> </semantics></math> and its approximation <math display="inline"><semantics> <mrow> <mover accent="true"> <mo>Δ</mo> <mo>˜</mo> </mover> <mo>????</mo> <mrow> <mo>(</mo> <mi>c</mi> <mo>)</mo> </mrow> </mrow> </semantics></math> versus the permissible cutoff point <span class="html-italic">c</span>. Data of sample size <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>50</mn> </mrow> </semantics></math> were generated from Model A in (<a href="#FD7-mathematics-12-03190" class="html-disp-formula">7</a>) with <math display="inline"><semantics> <mrow> <mi>β</mi> <mo>=</mo> <mn>0.2</mn> </mrow> </semantics></math>. The dark line corresponds to the goodness-of-split measures or splitting statistics <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mo>????</mo> <mo>(</mo> <mi>c</mi> <mo>)</mo> </mrow> </semantics></math> in greedy search, while the lines in gray scale are approximated <math display="inline"><semantics> <mrow> <mover accent="true"> <mo>Δ</mo> <mo>˜</mo> </mover> <mo>????</mo> <mrow> <mo>(</mo> <mi>c</mi> <mo>)</mo> </mrow> </mrow> </semantics></math> values in SSS with <math display="inline"><semantics> <mrow> <mi>a</mi> <mo>=</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mo>…</mo> <mo>,</mo> <mn>100</mn> </mrow> </semantics></math>. The red solid triangle point corresponds to the best cutpoint found by GS, while the blue disc points are the best cutpoints obtained from SSS with different <span class="html-italic">a</span> values. The solid green line corresponds to the true cutoff point <math display="inline"><semantics> <mrow> <msub> <mi>c</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>0.5</mn> </mrow> </semantics></math>.</p>
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<p>Plot of the logistic function <math display="inline"><semantics> <mrow> <mi>π</mi> <mo>{</mo> <mi>x</mi> <mo>;</mo> <mi>a</mi> <mo>}</mo> </mrow> </semantics></math> for different values of <math display="inline"><semantics> <mrow> <mi>a</mi> <mo>=</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mo>…</mo> <mo>,</mo> <mn>100</mn> </mrow> </semantics></math>. The dark line corresponds to the Heaviside step function <math display="inline"><semantics> <mrow> <mi>H</mi> <mo>(</mo> <mi>x</mi> <mo>)</mo> <mo>=</mo> <mi>I</mi> <mo>{</mo> <mi>x</mi> <mo>≤</mo> <mn>0</mn> <mo>}</mo> <mo>.</mo> </mrow> </semantics></math></p>
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<p>Empirical density of estimated cutpoint <math display="inline"><semantics> <mover accent="true"> <mi>c</mi> <mo stretchy="false">^</mo> </mover> </semantics></math>: SSS vs. GS (<b>a</b>–<b>j</b>). Ten scenarios were considered by combining two sample sizes <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>∈</mo> <mo>{</mo> <mn>50</mn> <mo>,</mo> <mn>500</mn> <mo>}</mo> </mrow> </semantics></math>, signal strength <math display="inline"><semantics> <mrow> <msub> <mi>β</mi> <mn>1</mn> </msub> <mo>∈</mo> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>0.2</mn> <mo>,</mo> <mn>1</mn> <mo>}</mo> </mrow> <mo>,</mo> </mrow> </semantics></math> and two true cutoff points <math display="inline"><semantics> <mrow> <msub> <mi>c</mi> <mn>0</mn> </msub> <mo>∈</mo> <mrow> <mo>{</mo> <mn>0.5</mn> <mo>,</mo> <mn>0.8</mn> <mo>}</mo> </mrow> </mrow> </semantics></math> (indicated via vertical blue lines). Each scenario was examined with 200 simulation runs. In each plot, the density curve of <math display="inline"><semantics> <mover accent="true"> <mi>c</mi> <mo stretchy="false">^</mo> </mover> </semantics></math> from GS is shaded and outlined in red. The <span class="html-italic">a</span> value in SSS falls within the range {1, 2, <span class="html-italic">…</span>, 100}, corresponding to the curves in grayscale, where darker colors represent larger <span class="html-italic">a</span> values.</p>
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<p>MSE of the estimated cutpoint <math display="inline"><semantics> <mover accent="true"> <mi>c</mi> <mo stretchy="false">^</mo> </mover> </semantics></math> vs. <span class="html-italic">a</span> in SSS. In Panels (<b>a</b>,<b>b</b>,<b>e</b>,<b>f</b>), the true cutpoint is <math display="inline"><semantics> <mrow> <msub> <mi>c</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>0.5</mn> </mrow> </semantics></math>, while in Panels (<b>c</b>,<b>d</b>,<b>g</b>,<b>h</b>) it is <math display="inline"><semantics> <mrow> <msub> <mi>c</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>0.8</mn> </mrow> </semantics></math>. The solid red horizontal line corresponds to the MSE value from GS.</p>
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<p>Plot of estimated cutoff point <math display="inline"><semantics> <mover accent="true"> <mi>c</mi> <mo stretchy="false">^</mo> </mover> </semantics></math> versus <math display="inline"><semantics> <mrow> <mi>a</mi> <mo>=</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mo>…</mo> <mo>,</mo> <mn>100</mn> </mrow> </semantics></math> for 100 simulation runs (<b>a</b>–<b>d</b>). Data were generated from Model A with <math display="inline"><semantics> <mrow> <mi>β</mi> <mo>=</mo> <mn>1</mn> <mo>.</mo> </mrow> </semantics></math> Each gray line corresponds to one simulation run. Superimposed on each plot are the true cutoff point (dotted red line) and mean cutoff at each <span class="html-italic">a</span> (solid green line). In Panel (<b>b</b>), the median cutoff is also added (solid blue line). Four scenarios were considered by combining two sample sizes <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>∈</mo> <mo>{</mo> <mn>50</mn> <mo>,</mo> <mn>500</mn> <mo>}</mo> </mrow> </semantics></math> and two true cutoff points <math display="inline"><semantics> <mrow> <msub> <mi>c</mi> <mn>0</mn> </msub> <mo>∈</mo> <mrow> <mo>{</mo> <mn>0.5</mn> <mo>,</mo> <mn>0.8</mn> <mo>}</mo> </mrow> <mo>.</mo> </mrow> </semantics></math></p>
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<p>Relative difference in MSE of SSS versus GS for different sample sizes <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>∈</mo> <mo>{</mo> <mn>50</mn> <mo>,</mo> <mn>100</mn> <mo>,</mo> <mn>150</mn> <mo>,</mo> <mo>…</mo> <mo>,</mo> <mn>1000</mn> <mo>}</mo> <mo>.</mo> </mrow> </semantics></math> A few constant <span class="html-italic">a</span> choices in {10, 30, 50} are considered for SSS, together with <span class="html-italic">n</span>-adaptive choices <math display="inline"><semantics> <mrow> <mo>{</mo> <mi>n</mi> <mo>,</mo> <msqrt> <mi>n</mi> </msqrt> <mo>,</mo> <mo form="prefix">ln</mo> <mrow> <mo>(</mo> <mi>n</mi> <mo>)</mo> </mrow> <mo>}</mo> <mo>.</mo> </mrow> </semantics></math> Negative values indicate advantages over GS.</p>
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<p>Computing time comparison between GS and SSS. The sample size <span class="html-italic">n</span> varies in <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>20</mn> <mo>,</mo> <mn>30</mn> <mo>,</mo> <mo>…</mo> <mo>,</mo> <mn>100</mn> <mo>,</mo> <mn>200</mn> <mo>,</mo> <mn>300</mn> <mo>,</mo> <mo>…</mo> </mrow> </semantics></math>, 10,000). The total CPU time (in seconds) for ten simulation runs in each setting was recorded for both GS and SSS. For SSS, the number <span class="html-italic">m</span> of iterative steps in Brent’s optimization algorithm was also obtained and averaged over ten simulation runs. Panel (<b>a</b>) plots the CPU computing time versus the sample size <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>.</mo> </mrow> </semantics></math> The computing times from GS are plotted with black circles and superimposed with a smooth curve from lowess. The curves from SSS with <math display="inline"><semantics> <mrow> <mi>a</mi> <mo>∈</mo> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mo>…</mo> <mo>,</mo> <mn>100</mn> <mo>}</mo> </mrow> </semantics></math> are plotted. In addition, an adaptive choice <math display="inline"><semantics> <mrow> <mi>a</mi> <mo>=</mo> <msqrt> <mi>n</mi> </msqrt> </mrow> </semantics></math> is also included and its associated computing times are plotted with gray diamonds. In Panel (<b>b</b>), the averaged number of iterative steps involved in Brent’s method are plotted vs. <span class="html-italic">n</span>.</p>
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<p>Bar plot of frequencies (from 1000 simulation runs) of splitting variables selected by SSS vs. greedy search. The data were generated from a null model. Nine variables <math display="inline"><semantics> <mrow> <mo>{</mo> <msub> <mi>X</mi> <mn>1</mn> </msub> <mo>,</mo> <msub> <mi>X</mi> <mn>2</mn> </msub> <mo>,</mo> <mo>…</mo> <mo>,</mo> <msub> <mi>X</mi> <mn>9</mn> </msub> <mo>}</mo> </mrow> </semantics></math>, with the possible number of distinct values equal to <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>4</mn> <mo>,</mo> <mn>5</mn> <mo>,</mo> <mn>10</mn> <mo>,</mo> <mn>20</mn> <mo>,</mo> <mn>50</mn> <mo>,</mo> <mn>100</mn> <mo>,</mo> <mn>500</mn> <mo>}</mo> </mrow> </semantics></math>, respectively, were included in each dataset. Two sample sizes <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>50</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>500</mn> </mrow> </semantics></math> were considered. For SSS, three choices of <math display="inline"><semantics> <mrow> <mi>a</mi> <mo>∈</mo> </mrow> </semantics></math> {10, 30, 50} were tried.</p>
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<p>Percentages of correct selection (out of 500 simulation runs) by GS vs. SSS: (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>50</mn> </mrow> </semantics></math> and (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>500</mn> <mo>.</mo> </mrow> </semantics></math> The data were generated from Model B in (<a href="#FD9-mathematics-12-03190" class="html-disp-formula">9</a>).</p>
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<p>Analysis of 1987 baseball salary data. In (<b>a</b>), <math display="inline"><semantics> <msub> <mi>S</mi> <mn>1</mn> </msub> </semantics></math> and <math display="inline"><semantics> <msub> <mi>S</mi> <mn>2</mn> </msub> </semantics></math> represent specific subsets of baseball teams. Within each terminal node is the mean response (log-transformed salary); underneath is the sample size.</p>
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<p>Comparison of SSS and GS in finding the best cutoff point <math display="inline"><semantics> <mrow> <mi>c</mi> <mo>=</mo> <mn>0.5</mn> </mrow> </semantics></math> for classification trees. The results are based on 500 simulation runs. Panels (<b>a</b>,<b>b</b>) plot the estimated density curves for <math display="inline"><semantics> <mover accent="true"> <mi>c</mi> <mo stretchy="false">^</mo> </mover> </semantics></math> with <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>50</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>500</mn> </mrow> </semantics></math>, respectively. Panel (<b>c</b>) is the scatterplot (smoothed in such a way that the frequencies of overlapped points are represented in the electromagnetic spectrum) of the cutoff point identified by GS versus that identified by SSS when <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>50</mn> <mo>.</mo> </mrow> </semantics></math> Panel (<b>d</b>) plots the MSE vs. <span class="html-italic">a</span>, superimposed as orange solid lines with MSE from GS.</p>
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<p>Comparison of SSS (combined with Boulesteix [<a href="#B42-mathematics-12-03190" class="html-bibr">42</a>]’s method) and GS in terms of selection bias for classification trees. The bar plots are based on frequencies (out of 500 simulation runs) of splitting. Variables were selected by either method. Data were generated from a null model. Two sample sizes of <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>50</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>n</mi> <mo>=</mo> <mn>500</mn> </mrow> </semantics></math> were considered.</p>
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<p>Final classification trees for the credit card default data. The misclassification error rates are 0.1792 for the SSS tree and 0.1798 for the GS tree.</p>
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13 pages, 16239 KiB  
Article
Anti-Obesity Effect of Fresh and Browned Magnolia denudata Flowers in 3T3-L1 Adipocytes
by Deok Jae Lee, Jae Ho Yeom, Yong Kwon Lee, Yong Hoon Joo and Namhyun Chung
Appl. Sci. 2024, 14(20), 9254; https://doi.org/10.3390/app14209254 - 11 Oct 2024
Viewed by 353
Abstract
The major components of magnolia flower extracts (MFEs) were classified into four substances, such as flavonoids, phenylethanoid glycoside derivatives (PhGs), caffeoylquinic acids (CQAs), and others, in our previous study. The chemical components of MFEs, including the rutin of flavonoid, acteoside and isoacteoside of [...] Read more.
The major components of magnolia flower extracts (MFEs) were classified into four substances, such as flavonoids, phenylethanoid glycoside derivatives (PhGs), caffeoylquinic acids (CQAs), and others, in our previous study. The chemical components of MFEs, including the rutin of flavonoid, acteoside and isoacteoside of PhGs, and caffeyolquinic acids, are reported to have physiological effects on anti-obesity effects. The anti-obesity effect of fresh and browned Magnolia denudata flower extracts (FMFE and BMFE, respectively) was investigated in 3T3-L1 adipocytes. The treatment concentrations of FMFE and BMFE were 200 and 400 μg/mL, respectively, as determined with the WST-1 assay. Intracellular lipid accumulation in 3T3-L1 cells was inhibited with the treatment of MFEs, including FMFE and BMFE, as observed with an image of the culture plate, using an optical microscope and Oil red O staining. The expression of the adipogenic target genes involved in adipocyte differentiation, including PPARγ, C/EBPα, perilipin, FABP4, FAS, HSL, and SREBP-1, was suppressed with the treatment of MFEs. Additionally, the phosphorylation of AMPK and ACC in 3T3-L1 cells was significantly increased following treatment with the MFEs. These results suggest that both MFEs have a potential for physiological effects on anti-obesity activity. Full article
(This article belongs to the Section Food Science and Technology)
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Figure 1
<p>Cell viability of various concentrations of the fresh and browned <span class="html-italic">Magnolia denudata</span> flower extracts (FMFE and BMFE). Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of the fresh and browned <span class="html-italic">Magnolia denudata</span> flower extracts (FMFE and BMFE) on the lipid accumulation of differentiating 3T3-L1 adipocytes. (<b>A</b>) Images of cell culture plates of 3T3-L1 adipocytes following the Oil red O staining of intracellular lipid droplets. (<b>B</b>) Images from a optical microscope of 3T3-L1 adipocytes following the Oil red O staining of intracellular lipid droplets. (<b>C</b>) Lipid contents of FMFE and BMFE groups. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of FMFE and BMFE on the expression of mRNA related to differentiation in 3T3-L1 adipocytes. (<b>A</b>) PPARγ, (<b>B</b>) C/EBPα, (<b>C</b>) SREBP-1, (<b>D</b>) FAS, (<b>E</b>) perilipin, (<b>F</b>) FABP4, (<b>G</b>) HSL. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of FMFE and BMFE on the expression genes related to differentiation in 3T3-L1 adipocytes. (<b>A</b>) PPARγ, (<b>B</b>) C/EBPα, (<b>C</b>) perilipin. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of FMFE and BMFE on the energy and lipid metabolism in 3T3-L1 adipocytes. (<b>A</b>) p-ACC, (<b>B</b>) p-AMPK. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Anti-adipogenesis effect of FMFE and BMFE in 3T3-L1 adipocytes. Red arrow indicates the increase and decrease in the expression of genes and proteins, and the observed phenomena.</p>
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31 pages, 42225 KiB  
Article
Comparative Insights into Photosynthetic, Biochemical, and Ultrastructural Mechanisms in Hibiscus and Pelargonium Plants
by Renan Falcioni, Werner Camargos Antunes, Roney Berti de Oliveira, Marcelo Luiz Chicati, José Alexandre M. Demattê and Marcos Rafael Nanni
Plants 2024, 13(19), 2831; https://doi.org/10.3390/plants13192831 - 9 Oct 2024
Viewed by 670
Abstract
Understanding photosynthetic mechanisms in different plant species is crucial for advancing agricultural productivity and ecological restoration. This study presents a detailed physiological and ultrastructural comparison of photosynthetic mechanisms between Hibiscus (Hibiscus rosa-sinensis L.) and Pelargonium (Pelargonium zonale (L.) L’Hér. Ex Aiton) [...] Read more.
Understanding photosynthetic mechanisms in different plant species is crucial for advancing agricultural productivity and ecological restoration. This study presents a detailed physiological and ultrastructural comparison of photosynthetic mechanisms between Hibiscus (Hibiscus rosa-sinensis L.) and Pelargonium (Pelargonium zonale (L.) L’Hér. Ex Aiton) plants. The data collection encompassed daily photosynthetic profiles, responses to light and CO2, leaf optical properties, fluorescence data (OJIP transients), biochemical analyses, and anatomical observations. The findings reveal distinct morphological, optical, and biochemical adaptations between the two species. These adaptations were associated with differences in photochemical (AMAX, E, Ci, iWUE, and α) and carboxylative parameters (VCMAX, ΓCO2, gs, gm, Cc, and AJMAX), along with variations in fluorescence and concentrations of chlorophylls and carotenoids. Such factors modulate the efficiency of photosynthesis. Energy dissipation mechanisms, including thermal and fluorescence pathways (ΦPSII, ETR, NPQ), and JIP test-derived metrics highlighted differences in electron transport, particularly between PSII and PSI. At the ultrastructural level, Hibiscus exhibited optimised cellular and chloroplast architecture, characterised by increased chloroplast density and robust grana structures. In contrast, Pelargonium displayed suboptimal photosynthetic parameters, possibly due to reduced thylakoid counts and a higher proportion of mitochondria. In conclusion, while Hibiscus appears primed for efficient photosynthesis and energy storage, Pelargonium may prioritise alternative cellular functions, engaging in a metabolic trade-off. Full article
(This article belongs to the Special Issue Photosynthesis and Carbon Metabolism in Higher Plants and Algae)
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Figure 1
<p>Representative of Hibiscus (<span class="html-italic">Hibiscus rosa-sinensis</span> L.) and Pelargonium (<span class="html-italic">Pelargonium zonale</span> (L.) L’Hér. Ex Aiton) plants. Hibiscus leaves exhibit a waxy surface and large size, while Pelargonium leaves are smaller, lobed, and covered with trichomes.</p>
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<p>Spectral analysis of leaves (in vivo) and pigments (in vitro) in Hibiscus and Pelargonium plants. (<b>A</b>) Reflectance factor (Ref) from 350 to 2500 nm. (<b>B</b>) Transmittance factor (Trans) from 350 to 2500 nm. (<b>C</b>) Absorbance factor (Abs) from 350 to 2500 nm. (<b>D</b>) Spectral analysis of chloroplast and extrachloroplast pigments from 350 to 750 nm, with specific peaks for chlorophylls (green arrow) and flavonoids (pink arrow). The solid lines represent the adaxial surface, and the dashed lines represent the abaxial surface. The arrows highlight peaks for chlorophyll and flavonoid concentrations. Blue arrows denote water-specific spectral signatures. Peak shifts indicate variations due to pigments such as chlorophylls, carotenoids, and phenolic compounds. (<span class="html-italic">n</span> = 100).</p>
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<p>Spectral analysis of leaves (in vivo) and pigments (in vitro) in Hibiscus and Pelargonium plants. (<b>A</b>) Reflectance factor (Ref) from 350 to 2500 nm. (<b>B</b>) Transmittance factor (Trans) from 350 to 2500 nm. (<b>C</b>) Absorbance factor (Abs) from 350 to 2500 nm. (<b>D</b>) Spectral analysis of chloroplast and extrachloroplast pigments from 350 to 750 nm, with specific peaks for chlorophylls (green arrow) and flavonoids (pink arrow). The solid lines represent the adaxial surface, and the dashed lines represent the abaxial surface. The arrows highlight peaks for chlorophyll and flavonoid concentrations. Blue arrows denote water-specific spectral signatures. Peak shifts indicate variations due to pigments such as chlorophylls, carotenoids, and phenolic compounds. (<span class="html-italic">n</span> = 100).</p>
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<p>Concentrations of compounds in Hibiscus and Pelargonium plants. (<b>A</b>) Chlorophyll a (g m<sup>−2</sup>). (<b>B</b>) Chlorophyll b (g m<sup>−2</sup>). (<b>C</b>) Total chlorophyll (<span class="html-italic">a</span>+<span class="html-italic">b</span>) (g m<sup>−2</sup>). (<b>D</b>) Carotenoids (g m<sup>−2</sup>). (<b>E</b>) Chl a/b ratio. (<b>F</b>) Car/Chl a+b ratio. (<b>G</b>) Flavonoids (nmol cm<sup>−2</sup>). (<b>H</b>) Phenolic compounds (mL cm<sup>−2</sup>). (<b>I</b>) Chlorophyll a (mg g<sup>−1</sup>). (<b>J</b>) Chlorophyll b (mg g<sup>−1</sup>). (<b>K</b>) Total chlorophyll (a+b) (mg g<sup>−1</sup>). (<b>L</b>) Carotenoids (mg g<sup>−1</sup>). (<b>M</b>) Flavonoids (μmol g<sup>−1</sup>). (<b>N</b>) Radical scavenging (% of antioxidant activity). (<b>O</b>) Lignin (mg g<sup>−1</sup>). (<b>P</b>) Cellulose (nmol mg<sup>−1</sup>). Asterisks over bars indicate statistically significant differences in the <span class="html-italic">t</span>-test (<span class="html-italic">p</span> &lt; 0.01). Mean ± SE (<span class="html-italic">n</span> = 100).</p>
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<p>Daily curves between 6 and 20 h were evaluated over three days for Hibiscus and Pelargonium plants. (<b>A</b>–<b>C</b>) Net assimilation rate (μmol CO<sub>2</sub> m<sup>−2</sup> s<sup>−1</sup>). (<b>D</b>–<b>F</b>) Internal CO<sub>2</sub> concentration (μmol CO<sub>2</sub> mol<sup>−1</sup>). (<b>G</b>–<b>H</b>) Net transpiration rate (mmol H<sub>2</sub>O m<sup>−2</sup> s<sup>−1</sup>). (<b>J</b>–<b>M</b>) Stomatal conductance (mol H<sub>2</sub>O m<sup>−2</sup> s<sup>−1</sup>). Black bars indicate darkness, and yellow bars indicate light environments. Mean ± SE (<span class="html-italic">n</span> = 20).</p>
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<p>Response curves for Hibiscus and Pelargonium plants. (<b>A</b>) Net photosynthetic light (<span class="html-italic">A</span>-PPFD) response. (<b>B</b>) Net photosynthetic CO<sub>2</sub> (<span class="html-italic">A</span>−<span class="html-italic">C</span><sub>i</sub>) responses. (<b>C</b>) Stomatal conductance (<span class="html-italic">g</span><sub>s</sub>) and transpiration rate (<span class="html-italic">E</span>). (<b>D</b>) Intrinsic water use efficiency (<span class="html-italic">i</span>WUE) response curves. The red arrow indicates the inflection point of 426 μmol mol<sup>−1</sup> CO<sub>2</sub> for decreased <span class="html-italic">C</span><sub>i</sub> in leaves. Mean ± SE (<span class="html-italic">n</span> = 10).</p>
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<p>Fluorescence response curves obtained simultaneously with the photosynthetic response to light in Hibiscus and Pelargonium plants. (<b>A</b>) Effective quantum yield of PSII (Fv’/Fm’). The inset shown in the bar graph indicates the maximum quantum yield of PSII (Fv/Fm) in dark−adapted leaves. (<b>B</b>) Operational efficiency of photosystem II (ΦPSII). The inset shows the electron transport rate (ETR). (<b>C</b>) Nonphotochemical quenching (NPQ). (<b>D</b>) Photochemical dissipation quenching (qP) and nonphotochemical dissipation quenching (qN). Asterisks over the bars indicate statistically significant differences according to the t-test (<span class="html-italic">p</span> &lt; 0.01). “ns” denotes no statistical significance. Mean ± SE (<span class="html-italic">n</span> = 10).</p>
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<p>Chlorophyll a fluorescence kinetic parameters derived from the JIP test in Hibiscus and Pelargonium plants. (<b>A</b>) Chlorophyll a fluorescence induction kinetics using normalised data. (<b>B</b>) Pipeline leaves display phenomenological energy flow through the excited cross-sections (CSs) of leaves. Yellow arrow—ABS/CS, absorption flow by approximate CS; green arrow—TR/CS, energy flow trapped by CS; red arrow—ET/CS, electron transport flow by CS; blue arrow—DI/CS, energy flow dissipated by CS; circles inscribed in squares—RC/CS indicate the % of active/inactive reaction centres. The white circles inscribed in squares represent reduced (active) QA reaction centres, the black circles represent non-reducing (inactive) QA reaction centres, and 100% of the active reaction centres responded with the highest average numbers observed in relation to Hibiscus. Arrow sizes indicate changes in the energy flow to Hibiscus plants. (<b>C</b>) ΨEO. (<b>D</b>) ΨRO. (<b>E</b>) ΦPO. (<b>F</b>) ΦPO. (<b>G</b>) ΦRO. (<b>H</b>) ΦDO. (<b>I</b>) δRO. (<b>J</b>) ρRO. (<b>K</b>) KN. (<b>L</b>) KP. (<b>M</b>) SFI<sub>ABS</sub>. (<b>N</b>) PI<sub>ABS</sub>. Different asterisks inside the arrows indicate significance, as determined by a <span class="html-italic">t</span>-test (<span class="html-italic">p</span> &lt; 0.01). Mean ± SE (<span class="html-italic">n</span> = 100).</p>
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<p>Representative images of optical microscopy (OM) in top–bottom and anatomical analyses of Hibiscus (first and second columns) and Pelargonium (third and fourth columns) plants. (<b>A</b>–<b>D</b>) Cross-sections. (<b>E</b>–<b>H</b>) Historesin cross-sections under false colour. (<b>I</b>–<b>L</b>) Details of the leaf thickness and cells. (<b>M</b>–<b>P</b>) Structures present in cellular tissues. Green arrows indicate chloroplasts, red arrows indicate diffuse crystals, and yellow arrows indicate dense cytoplasmic content. Accumulative and secretory structures of the adaxial epidermis are highlighted. Scale bars = 200 µm and 50 µm, left to right, respectively.</p>
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<p>Representative scanning electron microscopy (SEM) images of adaxial and abaxial surfaces of Hibiscus and Pelargonium plants. (<b>A</b>,<b>E</b>,<b>I</b>,<b>M</b>) Adaxial surface of the Hibiscus. (<b>B</b>,<b>F</b>,<b>J</b>,<b>N</b>) Abaxial surface of the Hibiscus. (<b>C</b>,<b>G</b>,<b>K</b>,<b>O</b>) Adaxial surface of Pelargonium. (<b>D</b>,<b>H</b>,<b>L</b>,<b>P</b>) Abaxial surface of Pelargonium. Scale bars = 250 μm (<b>A</b>–<b>D</b>), 150 μm (<b>E</b>–<b>H</b>), and 50 μm (<b>I</b>–<b>P</b>), top to bottom, respectively.</p>
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<p>Representative transmission electron microscopy (TEM) images of chloroplasts in Hibiscus and Pelargonium plants. (<b>A</b>,<b>B</b>,<b>E</b>,<b>F</b>,<b>I</b>,<b>J</b>,<b>M</b>,<b>N</b>,<b>Q</b>,<b>R</b>) Hibiscus. (<b>C</b>,<b>D</b>,<b>G</b>,<b>H</b>,<b>K</b>,<b>L</b>,<b>O</b>,<b>P</b>,<b>S</b>,<b>T</b>) Pelargonium plants. Scale bar = 4 μm (<b>A</b>–<b>D</b>), 1 μm (<b>E</b>–<b>P</b>) and 600 nm (<b>Q</b>–<b>T</b>).</p>
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<p>Representative transmission electron microscopy (TEM) images of mesophyll cells in the leaves. (<b>A</b>,<b>B</b>,<b>E</b>,<b>F</b>,<b>I</b>,<b>J</b>) Hibiscus. (<b>C</b>,<b>D</b>,<b>G</b>,<b>H</b>,<b>K</b>,<b>L</b>) Pelargonium plants. Scale bar = 4 μm (<b>A</b>–<b>D</b>), 1 μm (<b>E</b>–<b>P</b>) and 600 nm (<b>Q</b>–<b>T</b>).</p>
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<p>Multivariate analysis of Hibiscus and Pelargonium plants. The 2D PCA biplot of principal component analysis (PCA) displayed two dimensions (Dim1 and Dim2) and the contribution of the 20 most important variables to explain the formed clusters. See the abbreviation in <a href="#sec4-plants-13-02831" class="html-sec">Section 4</a>.</p>
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<p>Comparative scheme of Hibiscus and Pelargonium plants. It highlights the superior photosynthetic efficiency of Hibiscus, emphasising its enhanced cellular structure, including higher chloroplast density, which contributes to improved photosynthesis and energy storage. In contrast, Pelargonium exhibits cellular adjustments, including changes in thylakoid count and a higher proportion of mitochondria, suggesting resource allocation to alternative cellular functions. Detailed insets and labels elucidate the distinct morphological, biochemical, and photosynthetic adaptations between the two species. Thicker lines indicate more efficient electron flow in the electron transport chain. Elements of the figure were created using Biorender.com (accessed on 5 October 2024).</p>
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15 pages, 1421 KiB  
Article
The Effect of Nitrogen and Potassium Interaction on the Leaf Physiological Characteristics, Yield, and Quality of Sweet Potato
by Xing Shu, Minghuan Jin, Siyu Wang, Ximing Xu, Lijuan Deng, Zhi Zhang, Xu Zhao, Jing Yu, Yueming Zhu, Guoquan Lu and Zunfu Lv
Agronomy 2024, 14(10), 2319; https://doi.org/10.3390/agronomy14102319 - 9 Oct 2024
Viewed by 349
Abstract
This study selected two sweet potato varieties as research subjects and conducted a field experiment using a two-factor design with two potassium (K) levels (K0 and K1) and five nitrogen (N) levels (N0–N4). The physiological changes in sweet potato leaves under different N [...] Read more.
This study selected two sweet potato varieties as research subjects and conducted a field experiment using a two-factor design with two potassium (K) levels (K0 and K1) and five nitrogen (N) levels (N0–N4). The physiological changes in sweet potato leaves under different N and K treatments were measured, and nutrients such as the soluble sugar, protein, and starch content of sweet potato roots were analyzed. The results indicate that the activity of glutamine synthetase (GS) and the soluble protein content in sweet potato leaves increase first and then decrease with increasing N application, while K application can significantly increase the activity of GS and the soluble protein content. The N metabolic capacity of leaves is strongest when the fertilizer ratio is K1N2. The SPAD value of sweet potato leaves increases with increasing N application. The net photosynthetic rate, stomatal conductance, and intercellular CO2 concentration first increase and then decrease with increasing N application. K fertilizer has a significant effect on these parameters. As the N application rate increases, the starch and protein content in the tubers increase, while the soluble sugar content decreases. However, the number of tubers per plant, fresh weight of the tubers, and dry weight of the tubers increase initially and then decrease, while the vine length continuously increases. The application of K fertilizer can significantly increase the number of tubers per plant and stem thickness of sweet potato. In conclusion, the appropriate N–K combined application can promote N metabolism, enhance the photosynthetic capacity of sweet potato, increase yield, and improve quality. Full article
(This article belongs to the Special Issue Advances in Soil Fertility, Plant Nutrition and Nutrient Management)
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<p>Changes in soluble protein content in sweet potato leaves under different N and K levels. The letters on the column represent the significant difference at the 5% level. Columns with the same letter have no significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Changes in GS activity in sweet potato leaves under different N and K levels. The letters on the column represent the significant difference at the 5% level. Columns with the same letter have no significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Changes in SPAD value in sweet potato leaves under different N and K levels. The letters on the column represent the significant difference at the 5% level. Columns with the same letter have no significant difference at <span class="html-italic">p</span> &lt; 0.05. *** <span class="html-italic">p</span> &lt; 0.001.</p>
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