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21 pages, 5851 KiB  
Article
SAM-ResNet50: A Deep Learning Model for the Identification and Classification of Drought Stress in the Seedling Stage of Betula luminifera
by Shiya Gao, Hao Liang, Dong Hu, Xiange Hu, Erpei Lin and Huahong Huang
Remote Sens. 2024, 16(22), 4141; https://doi.org/10.3390/rs16224141 - 6 Nov 2024
Viewed by 373
Abstract
Betula luminifera, an indigenous hardwood tree in South China, possesses significant economic and ecological value. In view of the current severe drought situation, it is urgent to enhance this tree’s drought tolerance. However, traditional artificial methods fall short of meeting the demands [...] Read more.
Betula luminifera, an indigenous hardwood tree in South China, possesses significant economic and ecological value. In view of the current severe drought situation, it is urgent to enhance this tree’s drought tolerance. However, traditional artificial methods fall short of meeting the demands of breeding efforts due to their inefficiency. To monitor drought situations in a high-throughput and automatic approach, a deep learning model based on phenotype characteristics was proposed to identify and classify drought stress in B. luminifera seedlings. Firstly, visible-light images were obtained from a drought stress experiment conducted on B. luminifera shoots. Considering the images’ characteristics, we proposed an SAM-CNN architecture by incorporating spatial attention modules into classical CNN models. Among the four classical CNNs compared, ResNet50 exhibited superior performance and was, thus, selected for the construction of the SAM-CNN. Subsequently, we analyzed the classification performance of the SAM-ResNet50 model in terms of transfer learning, training from scratch, model robustness, and visualization. The results revealed that SAM-ResNet50 achieved an accuracy of 1.48% higher than that of ResNet50, at 99.6%. Furthermore, there was a remarkable improvement of 18.98% in accuracy, reaching 82.31% for the spatial transform images generated from the test set images by applying movement and rotation for robustness testing. In conclusion, the SAM-ResNet50 model achieved outstanding performance, with 99.6% accuracy and realized high-throughput automatic monitoring based on phenotype, providing a new perspective for drought stress classification and technical support for B. luminifera-related breeding work. Full article
(This article belongs to the Special Issue Intelligent Extraction of Phenotypic Traits in Agroforestry)
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Graphical abstract

Graphical abstract
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<p>Image acquisition platform for <span class="html-italic">Betula luminifera</span>.</p>
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<p>Sample images from the <span class="html-italic">B. luminifera</span> drought stress dataset (<b>a</b>–<b>f</b>) and from the moved and rotated datasets (<b>g</b>–<b>l</b>): (<b>a</b>) CG; (<b>b</b>) DR1; (<b>c</b>) DR2; (<b>d</b>) DR3; (<b>e</b>) DR4; (<b>f</b>) DR5; (<b>g</b>) moved down one-fifth to the left; (<b>h</b>) moved up one-sixth to the left; (<b>i</b>) moved down one-fifth to the right; (<b>j</b>) moved up one-sixth to the right; (<b>k</b>) turned 45° clockwise; (<b>l</b>) turned 45° counterclockwise.</p>
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<p>Workflow diagram.</p>
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<p>The SAM-CNN architecture.</p>
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<p>The change curves of the loss function value and accuracy during training: (<b>a</b>) loss function; (<b>b</b>) accuracy.</p>
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<p>The confusion matrixes describing the results of different models: (<b>a</b>) AlexNet; (<b>b</b>) VGG16; (<b>c</b>) GoogLeNet; (<b>d</b>) ResNet50; (<b>e</b>) SAM-ResNet50.</p>
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<p>The change curves of the loss function value and accuracy during training: (<b>a</b>) loss function; (<b>b</b>) accuracy.</p>
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<p>The change curves of the loss function value and accuracy during training: (<b>a</b>) loss function; (<b>b</b>) accuracy.</p>
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<p>The confusion matrixes describing the results of different models: (<b>a</b>) ResNet50; (<b>b</b>) SAM-ResNet50.</p>
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<p>Comparison of the visualization results before and after adding the SAM. The highlighted part of the class activation map represents the network’s attention on the image, with warmer colors indicating higher attention and cooler colors indicating lower attention: (<b>a</b>) the original image; (<b>b</b>) the area of attention before adding the attention mechanism; (<b>c</b>) the area of attention after adding the attention mechanism.</p>
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17 pages, 15092 KiB  
Article
Roles of Germin-like Protein Family in Response to Seed Germination and Shoot Branching in Brassica napus
by Qian Zhang, Luman Wang, Xinfa Wang, Jiangwei Qiao and Hanzhong Wang
Int. J. Mol. Sci. 2024, 25(21), 11518; https://doi.org/10.3390/ijms252111518 - 26 Oct 2024
Viewed by 508
Abstract
Germin-like proteins (GLPs) play important roles in the regulation of various plant development processes, such as seed vigor, root and leaf development and disease resistance, while the roles of GLPs on agronomic traits are rarely studied in Brassica napus. Here, we identified [...] Read more.
Germin-like proteins (GLPs) play important roles in the regulation of various plant development processes, such as seed vigor, root and leaf development and disease resistance, while the roles of GLPs on agronomic traits are rarely studied in Brassica napus. Here, we identified GLPs family genes in rapeseed and analyzed their potential functions. There are 77 GLPs family genes (BnGLPs) in the Zhongshuang11 rapeseed reference genome, divided into a, b, c, d, e, f six subfamilies. Tissue expression profile analysis of BnGLPs revealed the following: e subfamily genes were highly expressed in early stages of silique, cotyledon, vegetative rosette and leaf development; f subfamily genes were highly expressed in seed development; genes of a subfamily were mainly expressed in the root; and genes of b, c, d subfamily exhibited low-level or no expression in above mentioned tissues. RT-qPCR analysis confirmed that the transcripts of two f subfamily members decreased dramatically during seed germination, suggesting that f subfamily proteins may play vital roles in the early stage of seed germination. Transcriptome analysis of axillary buds in sequential developing stages revealed that the transcripts of eight e subfamily genes showed a rapid increase at the beginning of shoot branching, implying that the e subfamily members played vital roles in branch development. These results demonstrate that rapeseed BnGLPs likely play essential roles in seedling development, root development and plant architecture, indicating that harnessing certain BnGLPs may contribute to the improvement of rapeseed yield. Full article
(This article belongs to the Special Issue Advances in Brassica Crop Metabolism and Genetics)
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Figure 1

Figure 1
<p>Distribution of <span class="html-italic">GLPs</span> on <span class="html-italic">B. napus</span> chromosomes. In total, 77 <span class="html-italic">BnGLPs</span> were mapped on 18 chromosomes.</p>
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<p>Phylogenetic analysis of Germ-like proteins from <span class="html-italic">B. napus</span> and <span class="html-italic">A. thaliana</span>. The amino acid sequences of 77 <span class="html-italic">BnGLPs</span> and 32 <span class="html-italic">AtGLPs</span> were aligned by the MUSCLE tool. A phylogenetic tree was generated by MEGA using the neighbor-joining (NJ) method (bootstrap replications, n = 1000). The phylogenetic tree was highlighted with Evolview (version 3.0). The proteins are clustered into six distinct clades which were designated clade a to f, respectively. These clades were labeled with different colors.</p>
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<p>Genome-wide synteny analysis for <span class="html-italic">BnGLPs</span>. Gray lines indicate all the collinear blocks, and red lines highlight the orthologous relationships among <span class="html-italic">BnGLPs</span>.</p>
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<p>The phylogenetic relationship, exon-intron architecture and conserved motifs of 77 <span class="html-italic">BnGLPs</span> in <span class="html-italic">B. napus</span>. (<b>A</b>) The phylogenetic relationships of <span class="html-italic">BnGLPs</span> based on the NJ method. (<b>B</b>) The conserved motif composition of <span class="html-italic">BnGLPs</span>. (<b>C</b>) Gene structures of <span class="html-italic">BnGLPs</span>. Yellow boxes represent the untranslated regions (UTR), green boxes represent exons, and the gray lines represent introns.</p>
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<p>(<b>A</b>) Transcriptional expression profiles of 77 <span class="html-italic">BnGLPs</span> across different developmental stages and organs of ZS11 variety. (<b>B</b>–<b>F</b>) are relative expression levels of five <span class="html-italic">BnGLPs</span> in root, stem, leaf and silique. Error bars are standard deviations of three biological replicates. The color bar represents log10 expression values (Counts + 1). The color scale represents relative expression levels from low (blue color) to high (red color). DAF means days after flowering.</p>
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<p>Seed germination of ZS11, where 0 h refers to dry seed; 2 h, 4 h, 8 h, 16 h, 24 h, 48 h and 72 h refer to the different stages of seed imbibed in water, respectively.</p>
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<p>RT-qPCR analysis of expression differences in six genes at 0 h, 2 h, 4 h, 8 h, 16 h, 24 h and 48 h seed imbibed in water. Error bars are standard deviations of three biological replicates.</p>
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<p>RT-qPCR analysis of five genes expression level expressed in radicles, hypocotyls and cotyledons after 72 h and 120 h seed imbibed in water. Error bars are standard deviations of three biological replicates.</p>
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<p>The expression of <span class="html-italic">BnGLPs</span> family members in leaf under MeJA hormone treatment. The color bar represents log10 expression values (Counts + 1). The color scale represents relative expression levels from low (blue color) to high (red color).</p>
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<p>The expression of <span class="html-italic">BnGLPs</span> family members in different axillary buds. The color bar represents log10 expression values (Counts + 1) The color scale represents relative expression levels from low (blue color) to high (red color). S1 is the state of dormant axillary buds, S2 is the state of temporarily dormant axillary buds, S3 is the state of being activated axillary buds, S4 is the state of elongating axillary buds.</p>
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19 pages, 2479 KiB  
Article
Contrast Relative Humidity Response of Diverse Cowpea (Vigna unguiculata (L.) Walp.) Genotypes: Deep Study Using RNAseq Approach
by Ekaterina A. Krylova, Marina O. Burlyaeva, Varvara E. Tvorogova and Elena K. Khlestkina
Int. J. Mol. Sci. 2024, 25(20), 11056; https://doi.org/10.3390/ijms252011056 - 15 Oct 2024
Viewed by 609
Abstract
Cowpea (Vigna unguiculata (L.) Walp.) is appreciated for its suitability for cultivation and obtaining good yields in relatively extreme farming conditions. It is resistant to high temperatures and drought. Moreover, food products prepared from Vigna are rich in many nutrients such as [...] Read more.
Cowpea (Vigna unguiculata (L.) Walp.) is appreciated for its suitability for cultivation and obtaining good yields in relatively extreme farming conditions. It is resistant to high temperatures and drought. Moreover, food products prepared from Vigna are rich in many nutrients such as proteins, amino acids, carbohydrates, minerals, fiber, vitamins, and other bioactive compounds. However, in East and Southeast Asia, where the products of this crop are in demand, the climate is characterized by excessive humidity. Under these conditions, the vast majority of cowpea varieties tend to have indeterminate growth (elongated shoot length) and are unsuitable for mechanized harvesting. The molecular mechanisms for tolerance to high relative humidity remain the least studied in comparison with those for other abiotic stress factors (drought, heat, cold, flooding, etc.). The purpose of the work was to reveal and investigate differentially expressed genes in cowpea accessions having contrasting growth habits (determinate and indeterminate) under humid and drought conditions. We performed RNA-seq analysis using selected cowpea accessions from the VIR collection. Among the genotypes used, some have significant changes in their plant architecture in response to high relative humidity, while others were tolerant to these conditions. In total, we detected 1697 upregulated and 1933 downregulated genes. The results showed that phytohormone-related genes are involved in cowpea response to high relative humidity. DEGs associated with jasmonic acid signaling are proposed to be key contributors in the maintenance of compact architecture under humid conditions. Full article
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<p>Principal component analysis (PCA) plot of all expressed genes in the RNA–seq data. The <span class="html-italic">X</span>-axis indicates the first principal component; the <span class="html-italic">Y</span>-axis indicates the second principal component. The percentage of variance explained by each PC is shown in each case. Rose color—control group (the relative humidity was equal to 60%), blue color—experimental group (the relative humidity—90%). Analysis was performed with the DESeq2 package version 1.38.3.</p>
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<p>Volcano plot representing 24,350 differentially expressed genes. The <span class="html-italic">X</span>-axis indicates the log2-transformed gene expression fold changes between control group and experimental group of cowpea accessions. The <span class="html-italic">Y</span>-axis indicates the log10-transformed <span class="html-italic">p</span>-value. Dashed lines indicate log<sub>2</sub>FC and <span class="html-italic">p</span>-value thresholds. The scattered points represent each gene. Significant differentially upregulated genes are highlighted in red, significant differentially downregulated genes are highlighted in blue. Genes with a nonsignificant log<sub>2</sub>FC value and nonsignificant <span class="html-italic">p</span>-value are highlighted in black.</p>
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<p>Number of DEGs identified in a comparison between the control and experimental groups for each cowpea accession.</p>
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<p>Principal component analysis (PCA) plots and volcano plots of expressed genes in the RNA-seq data for four comparisons. (<b>1a</b>,<b>1b</b>) PCA plot and volcano plot for k6; (<b>2a</b>,<b>2b</b>) PCA plot and volcano plot for k642; (<b>3a</b>,<b>3b</b>) PCA plot and volcano plot for k1783; (<b>4a</b>,<b>4b</b>) PCA plot and volcano plot for k2056. The <span class="html-italic">X</span>-axis on the PCA plots indicates the first principal component; the <span class="html-italic">Y</span>-axis indicates the second principal component. The percentage of variance explained by each PC is shown in each case. Rose color—control group (the relative humidity was equal to 60%), blue color—experimental group (the relative humidity—90%). Analysis was performed with the DESeq2 package version 1.38.3. The <span class="html-italic">X</span>-axis on the volcano plots indicates the log2-transformed gene expression fold changes between the control group and experimental group of cowpea accession. The <span class="html-italic">Y</span>-axis indicates the log10-transformed <span class="html-italic">p</span>-value. Dashed lines indicate log<sub>2</sub>FC and <span class="html-italic">p</span>-value thresholds. The scattered points represent each gene. Significantly differentially upregulated genes are highlighted in red, and significantly differentially downregulated genes are high-lighted in blue. Genes with a nonsignificant log<sub>2</sub>FC value and nonsignificant <span class="html-italic">p</span>-value are highlighted in black.</p>
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<p>Venn diagrams representing the overlap between DEGs identified in four cowpea accessions in the control and experimental groups (two relative humidity conditions): (<b>a</b>) upregulated genes and (<b>b</b>) downregulated genes. Accessions are marked by different colors in letters.</p>
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<p>GO enrichment analysis of the (<b>a</b>) upregulated genes and (<b>b</b>) downregulated genes identified in four cowpea accessions in the control and experimental groups (two relative humidity conditions). For the BP categories, the top 50 GO terms are presented.</p>
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<p>Number of DEGs associated with plant hormone biosynthesis, metabolism, and signal transduction pathways. Genes identified in four cowpea accessions in the control and experimental groups (two relative humidity conditions): (<b>a</b>) upregulated genes and (<b>b</b>) downregulated genes.</p>
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<p>qRT-PCR validation of nine DEGs for k-2056 in high RH (experimental) versus low RH (control). Data were normalized to the expression of <span class="html-italic">VuUBQ10</span> (<span class="html-italic">Vigun07g244400</span>) encoding ubiquitin. Each sample was amplified in three technical replicates. Significant differences between the mean values are indicated (* <span class="html-italic">p</span> ≤ 0.001, ** <span class="html-italic">p</span> ≤ 0.05) (<span class="html-italic">t</span>-test).</p>
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<p>Cowpea accessions k-2056 (<b>a</b>,<b>c</b>) and k-642 (<b>b</b>,<b>d</b>) in two climatic chambers: (<b>a</b>,<b>b</b>) 60% RH (control group), (<b>c</b>,<b>d</b>) 90% RH (experimental group). The formation of climbing shoot for k-642 in high RH was observed (<b>d</b>), and for k-2056, there was no formation of such shoots (<b>c</b>).</p>
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13 pages, 1953 KiB  
Article
A Maize Mutant Impaired in SL Biosynthesis (zmccd8) Shows a Lower Growth, an Altered Response to Nitrogen Starvation, and a Potential Secondary Effect on Drought Tolerance
by Laura Ravazzolo, Andrea Chichi, Franco Meggio, Leonardo Buzzicotti, Benedetto Ruperti, Serena Varotto, Mario Malagoli and Silvia Quaggiotti
Stresses 2024, 4(4), 614-626; https://doi.org/10.3390/stresses4040039 - 25 Sep 2024
Viewed by 761
Abstract
Strigolactones (SLs) are essential phytohormones involved in plant development and interaction with the rhizosphere, regulating shoot branching, root architecture, and leaf senescence for nutrient reallocation. The Zea mays L. zmccd8 mutant, defective in SL biosynthesis, shows various architectural changes and reduced growth. This [...] Read more.
Strigolactones (SLs) are essential phytohormones involved in plant development and interaction with the rhizosphere, regulating shoot branching, root architecture, and leaf senescence for nutrient reallocation. The Zea mays L. zmccd8 mutant, defective in SL biosynthesis, shows various architectural changes and reduced growth. This study investigates zmccd8 and wild-type (WT) maize plants under two nutritional treatments (N-shortage vs. N-provision as urea). Morphometric analysis, chlorophyll and anthocyanin indexes, drought-related parameters, and gene expression were measured at specific time points. The zmccd8 mutant displayed reduced growth, such as shorter stems, fewer leaves, and lower kernel yield, regardless of the nutritional regime, confirming the crucial role of SLs. Additionally, zmccd8 plants exhibited lower chlorophyll content, particularly under N-deprivation, indicating SL necessity for proper senescence and nutrient mobilization. Increased anthocyanin accumulation in zmccd8 under N-shortage suggested a stress mitigation attempt, unlike WT plants. Furthermore, zmccd8 plants showed signs of increased water stress, likely due to impaired stomatal regulation, highlighting SLs role in drought tolerance. Molecular analysis confirmed higher expression of SL biosynthesis genes in WT under N-shortage, while zmccd8 lacked this response. These findings underscore SL importance in maize growth, stress responses, and nutrient allocation, suggesting potential agricultural applications for enhancing crop resilience. Full article
(This article belongs to the Topic Plant Responses to Environmental Stress)
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Figure 1
<p>Phenotypic analysis of stem height (<b>A</b>), leaf number (<b>B</b>), internode length (<b>C</b>), stem circumference (<b>D</b>), kernel weight (<b>E</b>), and ears length (<b>F</b>) for wild-type (WT) and <span class="html-italic">zmccd8</span> mutant plants at different days after sowing (DAS) under two N treatments. Error bars represent the mean ± SE (<span class="html-italic">n</span> = 24). At 58 DAS, urea was provided as the N source (dashed red line). Different letters indicate significant differences (at <span class="html-italic">p</span> &lt; 0.05 according to LSD test) at each DAS. Based on ANOVA, the significance of F values was reported as follows: ‘***’ <span class="html-italic">p</span> &lt; 0.001; ‘**’ <span class="html-italic">p</span> &lt; 0.01; ‘*’ <span class="html-italic">p</span> &lt; 0.05; no asterisks <span class="html-italic">p</span> &gt; 0.05.</p>
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<p>Profiles in chlorophyll content (<b>A</b>) and anthocyanin levels (<b>B</b>) in four different groups of maize leaves (L1-2; L3-4-5; L6-7-8; L9-10-11). Error bars represent the mean of six biological replicates ± SE. At 58 DAS, urea was provided as the N source (dashed red line). Different letters indicate significant differences (at <span class="html-italic">p</span> &lt; 0.05 according to LSD test) at each DAS. Based on ANOVA, the significance of F values was reported as follows: ‘***’ <span class="html-italic">p</span> &lt; 0.001; ‘**’ <span class="html-italic">p</span> &lt; 0.01; ‘*’ <span class="html-italic">p</span> &lt; 0.05; no asterisks <span class="html-italic">p</span> &gt; 0.05.</p>
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<p>Profiles of stomatal conductance (gsw, mol H<sub>2</sub>O m<sup>−2</sup>s<sup>−1</sup>) (<b>A</b>), leaf transpiration (E-app, mol H<sub>2</sub>O m<sup>−2</sup>s<sup>−1</sup>) (<b>B</b>), and photosystem II efficiency (PhiPS II) (<b>C</b>) in the group of leaves 9-10-11. Error bars represent the mean of six biological replicates ± SE. At 58 DAS, urea was provided as the N source (dashed red line). Different letters indicate significant differences (at <span class="html-italic">p</span> &lt; 0.05 according to LSD test) at each DAS. Based on ANOVA, the significance of F values was reported as follows: ‘***’ <span class="html-italic">p</span> &lt; 0.001; ‘*’ <span class="html-italic">p</span> &lt; 0.05; no asterisks <span class="html-italic">p</span> &gt; 0.05.</p>
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<p>Relative gene expression of three genes involved in SL biosynthesis (<span class="html-italic">CCD7</span>, <span class="html-italic">CCD8</span>), signalling (<span class="html-italic">MAX2</span>), and drought stress (<span class="html-italic">SULTR6</span>) in leaf samples at three different days after sowing (DAS). Data are means ± SE for three biological replicates. Different letters indicate significant differences (at <span class="html-italic">p</span> &lt; 0.05 according to LSD test) at each DAS. Based on ANOVA, the significance of F values was reported as follows: ‘***’ <span class="html-italic">p</span> &lt; 0.001; ‘**’ <span class="html-italic">p</span> &lt; 0.01; ‘*’ <span class="html-italic">p</span> &lt; 0.05; no asterisks <span class="html-italic">p</span> &gt; 0.05.</p>
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20 pages, 6666 KiB  
Article
Rhizofungus Aspergillus terreus Mitigates Heavy Metal Stress-Associated Damage in Triticum aestivum L.
by Naveen Dilawar, Muhammad Hamayun, Amjad Iqbal, Bokyung Lee, Sajid Ali, Ayaz Ahmad, Abdulwahed Fahad Alrefaei, Turki Kh. Faraj, Ho-Youn Kim and Anwar Hussain
Plants 2024, 13(18), 2643; https://doi.org/10.3390/plants13182643 - 21 Sep 2024
Viewed by 619
Abstract
Industrial waste and sewage deposit heavy metals into the soil, where they can remain for long periods. Although there are several methods to manage heavy metals in agricultural soil, microorganisms present a promising and effective solution for their detoxification. We isolated a rhizofungus, [...] Read more.
Industrial waste and sewage deposit heavy metals into the soil, where they can remain for long periods. Although there are several methods to manage heavy metals in agricultural soil, microorganisms present a promising and effective solution for their detoxification. We isolated a rhizofungus, Aspergillus terreus (GenBank Acc. No. KT310979.1), from Parthenium hysterophorus L., and investigated its growth-promoting and metal detoxification capabilities. The isolated fungus was evaluated for its ability to mitigate lead (25 and 75 ppm) and copper (100 and 200 ppm) toxicity in Triticum aestivum L. seedlings. The experiment utilized a completely randomized design with three replicates for each treatment. A. terreus successfully colonized the roots of wheat seedlings, even in the presence of heavy metals, and significantly enhanced plant growth. The isolate effectively alleviates lead and copper stress in wheat seedlings, as evidenced by increases in shoot length (142%), root length (98%), fresh weight (24%), dry weight (73%), protein content (31%), and sugar content (40%). It was observed that wheat seedlings possess a basic defense system against stress, but it was insufficient to support normal growth. Fungal inoculation strengthened the host’s defense system and reduced its exposure to toxic heavy metals. In treated seedlings, exposure to heavy metals significantly upregulated MT1 gene expression, which aided in metal detoxification, enhanced antioxidant defenses, and maintained metal homeostasis. A reduction in metal exposure was observed in several areas, including normalizing the activities of antioxidant enzymes that had been elevated by up to 67% following exposure to Pb (75 mg/kg) and Cu (200 mg/kg). Heavy metal exposure elevated antioxidant levels but also increased ROS levels by 86%. However, with Aspergillus terreus colonization, ROS levels stayed within normal ranges. This decrease in ROS was associated with reduced malondialdehyde (MDA) levels, enhanced membrane stability, and restored root architecture. In conclusion, rhizofungal colonization improved metal tolerance in seedlings by decreasing metal uptake and increasing the levels of metal-binding metallothionein proteins. Full article
(This article belongs to the Special Issue Role of Microbial Plant Biostimulants in Abiotic Stress Mitigation)
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<p>Assessment of the copper and lead tolerance potential of NB (<span class="html-italic">A. terreus</span>). The isolate was grown in shaking flasks (250 mL) containing 50 mL Czapek broth amended with different concentrations of Pb and Cu. Mean of triplicated data with standard error and letter labels for denoting significance are given (ANOVA-Duncan <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Colony morphologies on (<b>a</b>) a macroscopic and (<b>b</b>) a microscopic scale of the isolated rhizospheric fungi. (<b>c</b>) Phylogenetic tree based on ITS rDNA sequences of the rhizospheric fungal strain <span class="html-italic">A. terreus</span> was constructed.</p>
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<p>Release of soluble sugars and proteins by NB (<span class="html-italic">A. terreus</span>) fungus in response to varied amounts of lead acetate and copper sulfate stress. Data are the means of duplicates with standard error and letter labels denoting significance (ANOVA-Duncan <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Root length, shoot length, (<b>b</b>) fresh weight, and dry weight of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Chlorophyll a, and (<b>b</b>) chlorophyll b of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) SOD, (<b>b</b>) POD, (<b>c</b>) CAT, and (<b>d</b>) electrolyte leakage of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) H<sub>2</sub>O<sub>2</sub> and (<b>b</b>) MDA content assessment of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Total protein, and (<b>b</b>) sugar content assessment of <span class="html-italic">T. aestivum</span> L. in response to varied amounts of lead acetate and copper sulfate stress treated with NB (<span class="html-italic">A. terreus</span>). Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Colonization of the rhizofungus NB (<span class="html-italic">A. terreus</span>) in the roots of <span class="html-italic">T. aestivum</span> L. exposed to different concentrations of Pb and Cu; (<b>a</b>) control, (<b>b</b>) NB (<span class="html-italic">A. terreus</span>), (<b>c</b>) NB + Pb 25 ppm, (<b>d</b>) NB + Pb 75 ppm, (<b>e</b>) NB + Cu 100 ppm, (<b>f</b>) NB + Cu 200 ppm, (<b>g</b>) NB + Pb 25Cu100 ppm, (<b>h</b>) NB + Pb75Cu200 ppm. Root sections were stained with lactophenol cotton blue and observed under a light microscope at 40× magnification.</p>
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<p>Role of NB (<span class="html-italic">A. terreus</span>) with lead acetate [Pb(C<sub>2</sub>H<sub>3</sub>O<sub>2</sub>)<sub>2</sub>] and copper sulfate [CuSO<sub>4</sub>] on (<b>a</b>) phytochelatin (PC1) and (<b>b</b>) metallothionein (MT1) gene expression in <span class="html-italic">T. aestivum</span> L. cultivated in soil polluted with Pb and Cu. Data are the means of duplicates with standard error (Duncan test; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The scanning electron microscopy (SEM) picture of the root surface show the presence of strain <span class="html-italic">A. terreus</span> on it. (<b>A</b>) The root of <span class="html-italic">T. aestivum</span> plant without inoculation. (<b>B</b>) The fine structure of <span class="html-italic">T. aestivum</span> roots, subjected to both induced Pb and Cu stresses at the minutest level. (<b>C</b>) Hyphae of the <span class="html-italic">A. terreus</span> strain (the white arrows show the position). This activity was performed in Centralized Resource Laboratory (CRL), University of Peshawar.</p>
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<p>The scanning electron microscopy (SEM) picture of the root surface show the presence of strain <span class="html-italic">A. terreus</span> on it. (<b>A</b>) The root of <span class="html-italic">T. aestivum</span> plant without inoculation. (<b>B</b>) The fine structure of <span class="html-italic">T. aestivum</span> roots, subjected to both induced Pb and Cu stresses at the minutest level. (<b>C</b>) Hyphae of the <span class="html-italic">A. terreus</span> strain (the white arrows show the position). This activity was performed in Centralized Resource Laboratory (CRL), University of Peshawar.</p>
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16 pages, 5661 KiB  
Article
Genotype and Nitrogen Source Influence Drought Stress Response in Oil Palm Seedlings
by Rodrigo Ruiz-Romero, Marlon De la Peña, Iván Ayala-Díaz, Carmenza Montoya and Hernán Mauricio Romero
Agronomy 2024, 14(9), 2082; https://doi.org/10.3390/agronomy14092082 - 12 Sep 2024
Viewed by 568
Abstract
As a significant global source of vegetable oil, the oil palm’s ability to withstand abiotic stresses, particularly drought, is crucial for sustainable agriculture. This is especially significant in tropical regions, where water scarcity is becoming more common. Nitrogen, a vital nutrient, plays an [...] Read more.
As a significant global source of vegetable oil, the oil palm’s ability to withstand abiotic stresses, particularly drought, is crucial for sustainable agriculture. This is especially significant in tropical regions, where water scarcity is becoming more common. Nitrogen, a vital nutrient, plays an essential role in various physiological and biochemical processes in plants, directly influencing growth and stress tolerance. This study investigates the interaction between nitrogen sources (ammonium vs. nitrate) and drought stress in oil palm (Elaeis guineensis) seedlings, which is critical in enhancing productivity in this economically important crop. The experiment evaluated five commercial oil palm genotypes, which were supplied with nitrogen solutions (15 mM NH4+ or NO3) for 46 days, followed by 30 days of progressive drought. The results showed that drought conditions universally reduced the biomass, with ammonium-fed plants exhibiting greater shoot biomass sensitivity than nitrate-fed plants. Drought also significantly decreased the chlorophyll a, PhiPS2, and root-reducing sugar levels—critical indicators of photosynthetic efficiency and overall plant health. The effects on the root architecture were complex, with ammonium nutrition differentially influencing the lateral root length under well-watered versus drought conditions, highlighting nitrogen forms’ nuanced role in root development. Importantly, substantial genotypic variability was observed in most traits, affecting the responses to both the nitrogen source and drought stress. This variability suggests that certain genotypes may be better suited to cultivation in specific environmental conditions, particularly drought-prone areas. In conclusion, this study underscores the intricate interplay between nitrogen nutrition, genotypic variability, and drought tolerance in oil palm seedlings. These findings highlight the need to integrate these factors into agricultural management strategies to improve resilience and productivity in oil palm plantations. Full article
(This article belongs to the Section Plant-Crop Biology and Biochemistry)
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Figure 1
<p>Average dry weight of the shoots and roots of five oil palm genotypes across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watering). Statistical significance levels for the main effects and interactions among N sources (N), water availability (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, ** &lt;0.01, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>Root-to-shoot ratio for each genotype across two nitrogen forms (ammonium and nitrate) and two water conditions (drought and watered). Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (** &lt;0.01, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>The graph displays the average (<b>A</b>) total, (<b>B</b>) lateral, and (<b>C</b>) primary root length for each genotype across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watering). Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, ** &lt;0.01, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>Gas exchange for each genotype across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watered) after the imposition of water conditions: (<b>A</b>) net photosynthesis (A<sub>n</sub>), (<b>B</b>) stomatal conductance (g<sub>s</sub>), (<b>C</b>) substomatal CO<sub>2</sub> concentration (C<sub>i</sub>), and (<b>D</b>) transpiration rate (E). Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>Chlorophyll a fluorescence across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watered) after the imposition of water conditions: (<b>A</b>) quantum yield of photosystem II (PhiPS2) and (<b>B</b>) nonphotochemical quenching (NPQ). Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, ** &lt;0.01), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>Leaf metabolic content across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watered) after the imposition of water conditions: (<b>A</b>) chlorophyll a, (<b>B</b>) proteins, (<b>C</b>) amino acids, and (<b>D</b>) reducing sugars for each genotype. Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, ** &lt;0.01, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>Root metabolic content across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watered) after the imposition of water conditions: (<b>A</b>) proteins, (<b>B</b>) amino acids, and (<b>C</b>) reducing sugars for each genotype. Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, ** &lt;0.01, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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<p>Leaf mineral content across two different nitrogen forms (ammonium and nitrate) and two water conditions (drought and watered) after the imposition of water conditions: (<b>A</b>) nitrogen, (<b>B</b>) phosphorus, (<b>C</b>) potassium, (<b>D</b>) calcium, (<b>E</b>) magnesium, and (<b>F</b>) boron for each genotype. Statistical significance levels for the main effects and interactions among N sources (N), water conditions (W), and genotypes (G) are denoted by asterisks (* &lt;0.05, ** &lt;0.01, *** &lt;0.001), and nonsignificant results are labeled ns. Error bars represent standard errors (n = 5).</p>
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25 pages, 5935 KiB  
Article
Adaptive Responses of Hormones to Nitrogen Deficiency in Citrus sinensis Leaves and Roots
by Dan Hua, Rong-Yu Rao, Wen-Shu Chen, Hui Yang, Qian Shen, Ning-Wei Lai, Lin-Tong Yang, Jiuxin Guo, Zeng-Rong Huang and Li-Song Chen
Plants 2024, 13(14), 1925; https://doi.org/10.3390/plants13141925 - 12 Jul 2024
Cited by 2 | Viewed by 787
Abstract
Some citrus orchards in China often experience nitrogen (N) deficiency. For the first time, targeted metabolomics was used to examine N-deficient effects on hormones in sweet orange (Citrus sinensis (L.) Osbeck cv. Xuegan) leaves and roots. The purpose was to validate the [...] Read more.
Some citrus orchards in China often experience nitrogen (N) deficiency. For the first time, targeted metabolomics was used to examine N-deficient effects on hormones in sweet orange (Citrus sinensis (L.) Osbeck cv. Xuegan) leaves and roots. The purpose was to validate the hypothesis that hormones play a role in N deficiency tolerance by regulating root/shoot dry weight ratio (R/S), root system architecture (RSA), and leaf and root senescence. N deficiency-induced decreases in gibberellins and indole-3-acetic acid (IAA) levels and increases in cis(+)-12-oxophytodienoic acid (OPDA) levels, ethylene production, and salicylic acid (SA) biosynthesis might contribute to reduced growth and accelerated senescence in leaves. The increased ethylene formation in N-deficient leaves might be caused by increased 1-aminocyclopropanecarboxylic acid and OPDA and decreased abscisic acid (ABA). N deficiency increased R/S, altered RSA, and delayed root senescence by lowering cytokinins, jasmonic acid, OPDA, and ABA levels and ethylene and SA biosynthesis, increasing 5-deoxystrigol levels, and maintaining IAA and gibberellin homeostasis. The unchanged IAA concentration in N-deficient roots involved increased leaf-to-root IAA transport. The different responses of leaf and root hormones to N deficiency might be involved in the regulation of R/S, RSA, and leaf and root senescence, thus improving N use efficiency, N remobilization efficiency, and the ability to acquire N, and hence conferring N deficiency tolerance. Full article
(This article belongs to the Section Plant Response to Abiotic Stress and Climate Change)
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<p>Venn diagrams of HRMs detected in LN0, LN15, RN0, and RN15 (<b>A</b>), and total differentially abundant HRMs (<b>B</b>), upregulated HRMs (<b>C</b>), and downregulated HRMs (<b>D</b>) in LN0 vs. LN15 and RN0 vs. RN15.</p>
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<p>A PCoA plot of HRMs detected in leaves and roots from N0- and N15-treated <span class="html-italic">Citrus sinensis</span> seedlings.</p>
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<p>A diagram displaying the mean relative changes of AUXs in leaves (LN0/LN15; green) and roots (RN0/RN15; magenta). Data from <a href="#plants-13-01925-t001" class="html-table">Table 1</a>. In this Figure, we used italics for enzymes (proteins) and plain format for HRMs (AUXs). An asterisk indicated a significant difference between LN0 (RN0) and LN15 (RN15) at <span class="html-italic">p</span> &lt; 0.05. Also, an HRM was considered downregulated or upregulated when it was detected only in RN0 or LN0 (Inf) and RN15 or LN15 (fold change = 0) for a comparative group. AO1, aldehyde oxidase 1; ASB1, anthranilate synthase beta subunit 1; CYP83B1, cytochrome P450 83B1; DAO, dioxygenase for AUX oxidation; IAAId, indole-3-acetaldehyde; IAOx, indole-3-acetaldoxime; IGs, indole glucosinolates; IPyA, indole-3-pyruvic acid; MES17, methylesterase 17; oxIAA, 2-oxindole-3-acetic acid; PLC2, phosphoinositide phospholipase C 2; SATH, S-alkylthiohydroximate; SDRA, short-chain dehydrogenase/reductase; UGT74E2, UDP-glycosyltransferase 74E2; WAT1, Protein WALLS ARE THIN 1; YUC, indole-3-pyruvate monooxygenase YUCCA (refer to Ding et al. [<a href="#B44-plants-13-01925" class="html-bibr">44</a>]; Mano and Nemoto [<a href="#B39-plants-13-01925" class="html-bibr">39</a>]; Tognetti et al. [<a href="#B45-plants-13-01925" class="html-bibr">45</a>]; and Woodward and Bartel [<a href="#B40-plants-13-01925" class="html-bibr">40</a>]). The same notation will be used in <a href="#plants-13-01925-f004" class="html-fig">Figure 4</a>, <a href="#plants-13-01925-f005" class="html-fig">Figure 5</a>, <a href="#plants-13-01925-f006" class="html-fig">Figure 6</a> and <a href="#plants-13-01925-f007" class="html-fig">Figure 7</a>.</p>
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<p>A diagram displaying the mean relative changes of CKs in leaves (LN0/LN15; green) and roots (RN0/RN15; magenta). Data from <a href="#plants-13-01925-t001" class="html-table">Table 1</a>. An asterisk indicated a significant difference between LN0 (RN0) and LN15 (RN15) at <span class="html-italic">p</span> &lt; 0.05. Ade, adenine; Ado, adenosine; CKX, CK oxidase/dehydrogenase; CYP735A, cytochrome P450 monooxygenase, family 735, subfamily A (CK hydroxylase); DMAPP, dimethylallyl diphosphate; DZ, dihydrozeatin; DZR, DZ riboside; DZRMP, DZ riboside 5′-monophosphate; iPRDP, iP riboside 5′-diphosphate; iPRMP, iP riboside 5′-monophosphate; iPRTP, iP riboside 5′-triphosphate; tRNA-IPT, tRNA isopentenyltransferase; LOG, CK riboside 5′-monophosphate phosphoribohydrolase; tZRDP, tZR 5′-diphosphate; tZRMP, tZR 5′-monophosphate; tZRTP, tZR 5′-triphosphate; ZOGT, zeatin O-glucosyltransferase (refer to Hirose et al. [<a href="#B53-plants-13-01925" class="html-bibr">53</a>] and Sakakibara [<a href="#B38-plants-13-01925" class="html-bibr">38</a>]).</p>
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<p>A diagram displaying the mean relative changes of GAs in leaves (LN0/LN15; green) and roots (RN0/RN15; magenta). Data from <a href="#plants-13-01925-t001" class="html-table">Table 1</a>. An asterisk indicated a significant difference between LN0 (RN0) and LN15 (RN15) at <span class="html-italic">p</span> &lt; 0.05. CPS, <span class="html-italic">ent</span>-copalyl diphosphate synthase; GA2<sub>ox</sub>, GA 2-oxidase; GA3<sub>ox</sub>, GA 3-oxidase; GA20<sub>ox</sub>, GA 20-oxidase (refer to Binenbaum et al. [<a href="#B58-plants-13-01925" class="html-bibr">58</a>] and Yamaguchi [<a href="#B59-plants-13-01925" class="html-bibr">59</a>]).</p>
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<p>A diagram displaying the mean relative changes of JAs in leaves (LN0/LN15; green) and roots (RN0/RN15; magenta). Data from <a href="#plants-13-01925-t001" class="html-table">Table 1</a>. An asterisk indicated a significant difference between LN0 (RN0) and LN15 (RN15) at <span class="html-italic">p</span> &lt; 0.05. AOC, allene oxide cyclase; AOS, allene oxide synthase; 4CL, 4-coumarate--CoA ligase; Dihydro-OPDA, dihydro-12-oxo-phytodienoic acid; 12,13-EOT, 12,13-epoxyoctadecatrienoic acid; 13-HPOT, (13S)-hydroperoxyoctadecatrienoic acid; JAS, jasmonoyl amino acid synthetase; JMT, jasmonate O-methyltransferase; LOX, lipoxygenase; OPDA, 12-oxo-phytodienoic acid; OPR, 12-oxophytodienoate reductase (refer to Kienow et al. [<a href="#B73-plants-13-01925" class="html-bibr">73</a>]).</p>
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<p>A diagram displaying the mean relative changes of ABAs in leaves (LN0/LN15; green) and roots (RN0/RN15; magenta). Data from <a href="#plants-13-01925-t001" class="html-table">Table 1</a>. An asterisk indicated a significant difference between LN0 (RN0) and LN15 (RN15) at <span class="html-italic">p</span> &lt; 0.05. AAO3, abscisic-aldehyde oxidase; ABA2, xanthoxin dehydrogenase; ABA3, molybdenum cofactor sulfurase; CYP707A, ABA 8′-hydroxylase; NCED, 9-cis-epoxycarotenoid dioxygenase; ZEP, zeaxanthin epoxidase (refer to Chen et al. [<a href="#B91-plants-13-01925" class="html-bibr">91</a>] and Watanabe et al. [<a href="#B92-plants-13-01925" class="html-bibr">92</a>]).</p>
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<p>The schematic diagram of hormone responses to N deficiency in leaves and roots. Red, increase; Blue, decrease (refer to Lee and Yoon [<a href="#B116-plants-13-01925" class="html-bibr">116</a>] and Tian et al. [<a href="#B101-plants-13-01925" class="html-bibr">101</a>]).</p>
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18 pages, 2974 KiB  
Article
Computer Vision Method for Automatic Detection of Microstructure Defects of Concrete
by Alexey N. Beskopylny, Sergey A. Stel’makh, Evgenii M. Shcherban’, Irina Razveeva, Alexey Kozhakin, Besarion Meskhi, Andrei Chernil’nik, Diana Elshaeva, Oksana Ananova, Mikhail Girya, Timur Nurkhabinov and Nikita Beskopylny
Sensors 2024, 24(13), 4373; https://doi.org/10.3390/s24134373 - 5 Jul 2024
Viewed by 1164
Abstract
The search for structural and microstructural defects using simple human vision is associated with significant errors in determining voids, large pores, and violations of the integrity and compactness of particle packing in the micro- and macrostructure of concrete. Computer vision methods, in particular [...] Read more.
The search for structural and microstructural defects using simple human vision is associated with significant errors in determining voids, large pores, and violations of the integrity and compactness of particle packing in the micro- and macrostructure of concrete. Computer vision methods, in particular convolutional neural networks, have proven to be reliable tools for the automatic detection of defects during visual inspection of building structures. The study’s objective is to create and compare computer vision algorithms that use convolutional neural networks to identify and analyze damaged sections in concrete samples from different structures. Networks of the following architectures were selected for operation: U-Net, LinkNet, and PSPNet. The analyzed images are photos of concrete samples obtained by laboratory tests to assess the quality in terms of the defection of the integrity and compactness of the structure. During the implementation process, changes in quality metrics such as macro-averaged precision, recall, and F1-score, as well as IoU (Jaccard coefficient) and accuracy, were monitored. The best metrics were demonstrated by the U-Net model, supplemented by the cellular automaton algorithm: precision = 0.91, recall = 0.90, F1 = 0.91, IoU = 0.84, and accuracy = 0.90. The developed segmentation algorithms are universal and show a high quality in highlighting areas of interest under any shooting conditions and different volumes of defective zones, regardless of their localization. The automatization of the process of calculating the damage area and a recommendation in the “critical/uncritical” format can be used to assess the condition of concrete of various types of structures, adjust the formulation, and change the technological parameters of production. Full article
(This article belongs to the Section Fault Diagnosis & Sensors)
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<p>Photographs of concrete structure: (<b>a</b>) sample 1; (<b>b</b>) sample 2.</p>
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<p>U-Net.</p>
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<p>LinkNet.</p>
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<p>PSPnet-v1.</p>
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<p>PSPNet-v2.</p>
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<p>Photograph of concrete structure: (<b>a</b>) original image; (<b>b</b>) mask.</p>
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<p>Training: (<b>a</b>) U-Net; (<b>b</b>) LinkNet; (<b>c</b>) PSPNet-v1; (<b>d</b>) PSPNet-v2.</p>
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<p>Training: (<b>a</b>) U-Net; (<b>b</b>) LinkNet; (<b>c</b>) PSPNet-v1; (<b>d</b>) PSPNet-v2.</p>
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<p>Metric graphics: (<b>a</b>) U-Net; (<b>b</b>) LinkNet; (<b>c</b>) PSPNet-v1; (<b>d</b>) PSPNet-v2.</p>
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<p>Metric graphics: (<b>a</b>) U-Net; (<b>b</b>) LinkNet; (<b>c</b>) PSPNet-v1; (<b>d</b>) PSPNet-v2.</p>
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<p>Dispersion graph for the “defect” class: (<b>a</b>) U-Net; (<b>b</b>) LinkNet; (<b>c</b>) PSPNet-v1; (<b>d</b>) PSPNet-v2.</p>
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<p>Segmentation result: (<b>a</b>) the original image; (<b>b</b>) the original mask; (<b>c</b>) segmentation by the U-Net model; (<b>d</b>) segmentation by the LinkNet model; (<b>e</b>) segmentation by the PSPNet-v1 model; (<b>f</b>) segmentation by the PSPNet-v2 model.</p>
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<p>Segmentation result: (<b>a</b>) the original image; (<b>b</b>) the original mask; (<b>c</b>) segmentation by the U-Net model; (<b>d</b>) segmentation by the LinkNet model; (<b>e</b>) segmentation by the PSPNet-v1 model; (<b>f</b>) segmentation by the PSPNet-v2 model.</p>
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<p>The result of using a cellular automaton: (<b>a</b>) an improved mask; (<b>b</b>) an area dispersion graph.</p>
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20 pages, 14009 KiB  
Article
Canopy Architecture and Sun Exposure Influence Berry Cluster–Water Relations in the Grapevine Variety Muscat of Alexandria
by Olfa Zarrouk, Clara Pinto, Maria Victoria Alarcón, Alicia Flores-Roco, Leonardo Santos, Teresa S. David, Sara Amancio, Carlos M. Lopes and Luisa C. Carvalho
Plants 2024, 13(11), 1500; https://doi.org/10.3390/plants13111500 - 29 May 2024
Viewed by 1439
Abstract
Climate-change-related increases in the frequency and intensity of heatwaves affect viticulture, leading to losses in yield and grape quality. We assessed whether canopy-architecture manipulation mitigates the effects of summer stress in a Mediterranean vineyard. The Vitis vinifera L variety Muscat of Alexandria plants [...] Read more.
Climate-change-related increases in the frequency and intensity of heatwaves affect viticulture, leading to losses in yield and grape quality. We assessed whether canopy-architecture manipulation mitigates the effects of summer stress in a Mediterranean vineyard. The Vitis vinifera L variety Muscat of Alexandria plants were monitored during 2019–2020. Two canopy shoot-positioning treatments were applied: vertical shoot positioning (VSP) and modulated shoot positioning (MSP). In MSP, the west-side upper foliage was released to promote partial shoot leaning, shading the clusters. Clusters were sampled at pea size (PS), veraison (VER), and full maturation (FM). Measurements included rachis anatomy and hydraulic conductance (Kh) and aquaporins (AQP) and stress-related genes expression in cluster tissues. The results show significant seasonal and interannual differences in Kh and vascular anatomy. At VER, the Kh of the rachis and rachis+pedicel and the xylem diameter decreased but were unaffected by treatments. The phloem–xylem ratio was either increased (2019) or reduced (2020) in MSP compared to VSP. Most AQPs were down-regulated at FM in pedicels and up-regulated at VER in pulp. A potential maturation shift in MSP was observed and confirmed by the up-regulation of several stress-related genes in all tissues. The study pinpoints the role of canopy architecture in berry–water relations and stress response during ripening. Full article
(This article belongs to the Special Issue Grapevine Response to Abiotic Stress)
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<p>Anatomy of peduncle. (<b>A</b>) Complete cross section of FM in VSP from 2019, stained with Toluidine Blue. Scale bar: 1000 μm. (<b>B</b>) Cross section of PS in MSP from 2020 stained with Safranin and Astra Blue. Both lignified secondary xylem cells and sclerenchyma cells turn reddish with safranin. Scale bar: 100 μm. (<b>C</b>) Details of a vascular bundle of VER in MSP from 2020 stained with Toluidine Blue. Scale bar: 100 μm. Arrows indicate radio-medullary parenchyma rays. Abbreviations: C: cambium; Cx: cortex; OCx and ICx indicate the outer and inner layers of cortex parenchyma. Ep: epidermis; P: pith; PP: primary phloem; PX: primary xylem; S: sclerenchyma; SP: secondary phloem; SX: secondary xylem; t: tracheid; v: vessel; VB: vascular bundle.</p>
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<p>Details of vascular tissue areas at FM stained with Safranin and Astra Blue. In 2019, a significant decrease in xylem and phloem areas in MSP (<b>B</b>) when compared to VSP (<b>A</b>). In 2020, the xylem area is increased in MSP (<b>C</b>) versus VSP (<b>D</b>). Scale bars: 100 μm.</p>
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<p>Morpho-anatomical parameters and quantitative characteristics of vascular tissue of Muscat of Alexandria peduncle at three developmental stages during the 2019 and 2020 seasons under different shoot-positioning treatments (VSP and MSP) at three different phenological stages (pea size, PS; veraison, VER; and full maturation, FM). For each parameter, different letters indicate significant differences between sampling times for VSP (lower-case) or MSP (upper-case), while * indicates significant differences between treatments at the same sampling time and are indicated in the MSP square (ANOVA and Tukey’s HSD. <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Specific hydraulic conductivity Kh (Kg s<sup>−1</sup> MPa<sup>−1</sup> m<sup>−1</sup> Berry<sup>−1</sup>) in cluster (rachis+pedicel) and in rachis (normalized to cluster length and berry number) at five phenological stages (pea size (PS), beginning of veraison (VER<sub>i</sub>), end of veraison (VER<sub>f</sub>), mid-ripening (MR), and full maturation (FM)) of the Muscat of Alexandria variety conducted in VSP and MSP in 2019 (<b>A</b>,<b>B</b>) and 2020 (<b>C</b>,<b>D</b>) seasons. Data are means ± SE (<span class="html-italic">n</span> = 5).</p>
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<p>Pedicel conductivity contribution to the total cluster (rachis+pedicel) hydraulic conductivity (%) at five phenological stages (pea size (PS), beginning of veraison (VER<sub>i</sub>), end of veraison (VER<sub>f</sub>), mid-ripening (MR), full maturation (FM)) of the Muscat of Alexandria variety trained in VSP and MSP during 2019 and 2020 seasons. Data are means ± SE (<span class="html-italic">n</span> = 4). Comparisons between treatments at the same sampling time were performed by Student’s <span class="html-italic">t</span>-test (*: <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>Expression of genes coding for aquaporins of the PIP (plasma membrane intrinsic proteins), TIP (tonoplast intrinsic proteins), NIP (nodulin26-like intrinsic proteins), and SIP (small basic intrinsic proteins) subfamilies (log<sub>2</sub>(fold change)) during the berry maturation stages (pea size (PS), veraison (VER), and full maturation both at east (FM<sub>east</sub>) and west side (FM<sub>west</sub>)) in pedicel, pulp, and skin of the Muscat of Alexandria variety. Relative values for the treatmentsMSP are expressed in comparison to VSP. White boxes correspond to not-detected gene expression.</p>
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<p>Stress-related genes <span class="html-italic">VviAPX1</span>, <span class="html-italic">VviCOX6B</span>, <span class="html-italic">VviHSP20</span>; <span class="html-italic">VviHSP22</span>, <span class="html-italic">VviHSP23.6</span>, <span class="html-italic">VviP450</span>, <span class="html-italic">VviRINGU</span>, <span class="html-italic">VviUG1P</span>, <span class="html-italic">VviWRKY40</span> gene expression (log<sub>2</sub>(fold change)), during the grape maturation stages (pea size (PS), veraison (VER), and full maturation both at east (FM<sub>east</sub>) and west side (FM<sub>west</sub>)) in pedicel, pulp, and skin of Muscat of Alexandria variety. Relative values for the treatment MSP are expressed in comparison to VSP.</p>
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16 pages, 4859 KiB  
Article
FLsM: Fuzzy Localization of Image Scenes Based on Large Models
by Weiyi Chen, Lingjuan Miao, Jinchao Gui, Yuhao Wang and Yiran Li
Electronics 2024, 13(11), 2106; https://doi.org/10.3390/electronics13112106 - 29 May 2024
Viewed by 779
Abstract
This article primarily focuses on the study of image-based localization technology. While traditional methods have made significant advancements in technology and applications, the emerging field of visual image-based localization technology demonstrates tremendous potential for research. Deep learning has exhibited a strong performance in [...] Read more.
This article primarily focuses on the study of image-based localization technology. While traditional methods have made significant advancements in technology and applications, the emerging field of visual image-based localization technology demonstrates tremendous potential for research. Deep learning has exhibited a strong performance in image processing, particularly in developing visual navigation and localization techniques using large-scale visual models. This paper introduces a sophisticated scene image localization technique based on large models in a vast spatial sample environment. The study involved training convolutional neural networks using millions of geographically labeled images, extracting image position information using large model algorithms, and collecting sample data under various conditions in elastic scene space. Through visual computation, the shooting position of photos was inferred to obtain the approximate position information of users. This method utilizes geographic location information to classify images and combines it with landmarks, natural features, and architectural styles to determine their locations. The experimental results show variations in positioning accuracy among different models, with the most optimal model obtained through training on a large-scale dataset. They also indicate that the positioning error in urban street-based images is relatively small, whereas the positioning effect in outdoor and local scenes, especially in large-scale spatial environments, is limited. This suggests that the location information of users can be effectively determined through the utilization of geographic data, to classify images and incorporate landmarks, natural features, and architectural styles. The study’s experimentation indicates the variation in positioning accuracy among different models, highlighting the significance of training on a large-scale dataset for optimal results. Furthermore, it highlights the contrasting impact on urban street-based images versus outdoor and local scenes in large-scale spatial environments. Full article
(This article belongs to the Special Issue Advances in Social Bots)
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<p>Schematic diagram of image fuzzy positioning.</p>
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<p>Flow description of image positioning algorithm.</p>
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<p>Overall framework of elastic spatial positioning.</p>
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<p>Visual fuzzy positioning process based on large model.</p>
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<p>Image and text information fusion processing positioning.</p>
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<p>Overall framework of the FLsM structure, integrating image and text large models.</p>
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<p>Schematic diagram of global distribution of image dataset.</p>
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<p>Experimental results under different models.</p>
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<p>Relationship between positioning accuracy of different datasets under different models.</p>
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20 pages, 9321 KiB  
Article
Research on Road Pattern Recognition of a Vision-Guided Robot Based on Improved-YOLOv8
by Xiangyu Zhang and Yang Yang
Appl. Sci. 2024, 14(11), 4424; https://doi.org/10.3390/app14114424 - 23 May 2024
Viewed by 922
Abstract
In order to promote the accurate recognition and application of visual navigation robots to the environment, this paper carried out research on the road pattern recognition of a vision-guided robot based on improved YOLOv8 on the basis of road pattern calibration and experimental [...] Read more.
In order to promote the accurate recognition and application of visual navigation robots to the environment, this paper carried out research on the road pattern recognition of a vision-guided robot based on improved YOLOv8 on the basis of road pattern calibration and experimental sampling. First, an experimental system for road image shooting was built independently, and 21 different kinds of road pattern image data were obtained by sampling roads with different weather conditions, road materials, and degrees of damage. Second, the road pattern recognition model based on the classical neural network Resnet 18 was constructed for model training and testing, and the initial recognition of road pattern was realized. Third, the YOLOv8 target detection model was introduced to build the road pattern recognition model based on YOLOv8n, and the model was trained and tested, improving road pattern recognition accuracy and recognition response speed by 3.1% and 200%, respectively. Finally, to further improve the accuracy of road pattern recognition, improvement research was carried out on the YOLOv8n road pattern recognition model based on the C2f-ODConv module, the AWD adaptive weight downsampling module, the EMA attention mechanism, and the collaboration of the three modules. Three network architectures, classical CNN (Resnet 18), YOLOv8n, and improved YOLOv8n, were compared. The results show that four different optimization models can further improve the accuracy of road pattern recognition, among which the accuracy of the improved YOLO v8 road pattern recognition model based on multimodule cooperation is the highest, reaching more than 93%. Full article
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<p>Pavement image capture system.</p>
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<p>Pavements with different conditions.</p>
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<p>Pavements with different conditions.</p>
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<p>Network structure of Resnet 18.</p>
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<p>Classification principle of the YOLO v8n algorithm.</p>
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<p>C2f-ODConv module structure.</p>
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<p>Improved YOLO v8 pavement recognition model based on the C2f-ODConv module.</p>
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<p>AWD structure.</p>
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<p>Improved YOLO v8 pavement recognition model based on the AWD adaptive weight downsampling module.</p>
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<p>EMA structure.</p>
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<p>The improved YOLO v8 pavement recognition model based on the EMA attention mechanism module.</p>
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<p>Improved YOLO v8 road recognition model based on multimodule collaboration.</p>
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22 pages, 23766 KiB  
Article
Fine-Grained Feature Perception for Unmanned Aerial Vehicle Target Detection Algorithm
by Shi Liu, Meng Zhu, Rui Tao and Honge Ren
Drones 2024, 8(5), 181; https://doi.org/10.3390/drones8050181 - 3 May 2024
Viewed by 1556
Abstract
Unmanned aerial vehicle (UAV) aerial images often present challenges such as small target sizes, high target density, varied shooting angles, and dynamic poses. Existing target detection algorithms exhibit a noticeable performance decline when confronted with UAV aerial images compared to general scenes. This [...] Read more.
Unmanned aerial vehicle (UAV) aerial images often present challenges such as small target sizes, high target density, varied shooting angles, and dynamic poses. Existing target detection algorithms exhibit a noticeable performance decline when confronted with UAV aerial images compared to general scenes. This paper proposes an outstanding small target detection algorithm for UAVs, named Fine-Grained Feature Perception YOLOv8s-P2 (FGFP-YOLOv8s-P2), based on YOLOv8s-P2 architecture. We specialize in improving inspection accuracy while meeting real-time inspection requirements. First, we enhance the targets’ pixel information by utilizing slice-assisted training and inference techniques, thereby reducing missed detections. Then, we propose a feature extraction module with deformable convolutions. Decoupling the learning process of offset and modulation scalar enables better adaptation to variations in the size and shape of diverse targets. In addition, we introduce a large kernel spatial pyramid pooling module. By cascading convolutions, we leverage the advantages of large kernels to flexibly adjust the model’s attention to various regions of high-level feature maps, better adapting to complex visual scenes and circumventing the cost drawbacks associated with large kernels. To match the excellent real-time detection performance of the baseline model, we propose an improved Random FasterNet Block. This block introduces randomness during convolution and captures spatial features of non-linear transformation channels, enriching feature representations and enhancing model efficiency. Extensive experiments and comprehensive evaluations on the VisDrone2019 and DOTA-v1.0 datasets demonstrate the effectiveness of FGFP-YOLOv8s-P2. This achievement provides robust technical support for efficient small target detection by UAVs in complex scenarios. Full article
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<p>Network Architecture of FGFP-YOLOv8s-P2.</p>
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<p>Example of slicing operation.</p>
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<p>DC2-DCNv3 network architecture.</p>
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<p>Architecture of C2f and DC2-DCNv3-C2f modules.</p>
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<p>LSKA and LSPPF Module Structures.</p>
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<p>Random Partial Convolution Structure (RPConV).</p>
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<p>Illustrates the structure of the Random FasterNet Block.</p>
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<p>Influence of Different Feature Extraction Modules on the Model Training Process.</p>
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<p>Impact of Different Lightweight Modules on the Training Process of the Model on the DOTA Dataset.</p>
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<p>Exemplary Detection Results on the VisDrone2019 Test Set. (<b>a</b>) Insufficient lighting, small targets. (<b>b</b>) At night, small targets. (<b>c</b>) Insufficient lighting, small targets. (<b>d</b>) Complex background, insufficient lighting, small targets.</p>
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<p>Exemplary Detection Results on the GUDT-HWD Test Set.</p>
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<p>Grad-CAM Visualization of Shallow and Deep Layers in the Backbone Network. (<b>a</b>) Insufficient lighting, small targets. (<b>b</b>) Insufficient lighting, small targets. (<b>c</b>) At night, small targets. (<b>d</b>) At night, small targets.</p>
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16 pages, 31750 KiB  
Article
A Deep Learning Method for Log Diameter Measurement Using Wood Images Based on Yolov3 and DeepLabv3+
by Zhenglan Lu, Huilu Yao, Yubiao Lyu, Sheng He, Heng Ning, Yuhui Yu, Lixia Zhai and Lin Zhou
Forests 2024, 15(5), 755; https://doi.org/10.3390/f15050755 - 25 Apr 2024
Cited by 1 | Viewed by 1422
Abstract
Wood volume is an important indicator in timber trading, and log diameter is one of the primary parameters used to calculate wood volume. Currently, the most common methods for measuring log diameters are manual measurement or visual estimation by log scalers, which are [...] Read more.
Wood volume is an important indicator in timber trading, and log diameter is one of the primary parameters used to calculate wood volume. Currently, the most common methods for measuring log diameters are manual measurement or visual estimation by log scalers, which are laborious, time consuming, costly, and error prone owing to the irregular placement of logs and large numbers of roots. Additionally, this approach can easily lead to misrepresentation of data for profit. This study proposes a model for automatic log diameter measurement that is based on deep learning and uses images to address the existing problems. The specific measures to improve the performance and accuracy of log-diameter detection are as follows: (1) A dual network model is constructed combining the Yolov3 algorithm and DeepLabv3+ architecture to adapt to different log-end color states that considers the complexity of log-end faces. (2) AprilTag vision library is added to estimate the camera position during image acquisition to achieve real-time adjustment of the shooting angle and reduce the effect of log-image deformation on the results. (3) The backbone network is replaced with a MobileNetv2 convolutional neural network to migrate the model to mobile devices, which reduces the number of network parameters while maintaining detection accuracy. The training results show that the mean average precision of log-diameter detection reaches 97.28% and the mean intersection over union (mIoU) of log segmentation reaches 92.22%. Comparisons with other measurement models demonstrate that the proposed model is accurate and stable in measuring log diameter under different environments and lighting conditions, with an average accuracy of 96.26%. In the forestry test, the measurement errors for the volume of an entire truckload of logs and a single log diameter are 1.20% and 0.73%, respectively, which are less than the corresponding error requirements specified in the industry standards. These results indicate that the proposed method can provide a viable and cost-effective solution for measuring log diameters and offering the potential to improve the efficiency of log measurement and promote fair trade practices in the lumber industry. Full article
(This article belongs to the Section Wood Science and Forest Products)
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<p>Flowchart of log diameter measurement.</p>
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<p>Examples of stacked wood end images, capturing in different scenes: (<b>a</b>) in the forest farm and (<b>b</b>) at the wood factory.</p>
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<p>Examples of annotated images for Yolov3: (<b>a</b>) original image and (<b>b</b>) annotation.</p>
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<p>Examples of annotated images for DeepLabv3+. With each group of images separated by a dashed line, red and black represent the log-section labeling and background, respectively.</p>
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<p>The structure of MobileNetv2-Yolov3.</p>
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<p>The structure of MobileNetv2-DeepLabv3+.</p>
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<p>Schematic diagram and curves of the pixel length of AprilTag codes changing with shooting angle. (<b>a</b>) Shooting schematic diagram, (<b>b</b>) AprilTag A, (<b>c</b>) AprilTag B, and (<b>d</b>) AprilTag C.</p>
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<p>Accuracy change curves for different initial learning rates. (<b>a</b>) Yolov3 and (<b>b</b>) DeepLabv3+.</p>
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<p>Training loss values and accuracy change curves for: (<b>a</b>) Yolov3 and (<b>b</b>) DeepLabv3+.</p>
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<p>Example of a process for measuring log diameter: (<b>a</b>) original image, (<b>b</b>) Yolov3 detection, (<b>c</b>) DeepLabv3+ segmentation, and (<b>d</b>) ellipse fitting.</p>
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<p>Log diameter measurements in different scenarios: (<b>a</b>) truck and (<b>b</b>) timber yard.</p>
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<p>Log end face segmentation images using different methods: (<b>a</b>) original image, (<b>b</b>) dual-network, (<b>c</b>) K-means, and (<b>d</b>) HSV.</p>
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<p>Segmentation accuracy of different methods for each test image.</p>
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<p>The log diameter measurement process image.</p>
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21 pages, 10034 KiB  
Article
Rail-STrans: A Rail Surface Defect Segmentation Method Based on Improved Swin Transformer
by Chenghao Si, Hui Luo, Yuelin Han and Zhiwei Ma
Appl. Sci. 2024, 14(9), 3629; https://doi.org/10.3390/app14093629 - 25 Apr 2024
Viewed by 1104
Abstract
With the continuous expansion of the transport network, the safe operation of high-speed railway rails has become a crucial issue. Defect detection on the surface of rails is a key part of ensuring the safe operation of trains. Despite the progress of deep [...] Read more.
With the continuous expansion of the transport network, the safe operation of high-speed railway rails has become a crucial issue. Defect detection on the surface of rails is a key part of ensuring the safe operation of trains. Despite the progress of deep learning techniques in defect detection on the rails’ surface, there are still challenges related to various problems, such as small datasets and the varying scales of defects. Based on this, this paper proposes an improved encoder–decoder architecture based on Swin Transformer network, named Rail-STrans, which is specifically designed for intelligent segmentation of high-speed rail surface defects. The problem of a small and black-and-white rail dataset is solved using self-made large and multiple rail surface defect datasets through field shooting, data labelling, and data expansion. In this paper, two Local Perception Modules (LPMs) are added to the encoding network, which helps to obtain local context information and improve the accuracy of detection. Then, the Multiscale Feature Fusion Module (MFFM) is added to the decoding network, which helps to effectively fuse the feature information of defects at different scales in the decoding process and improves the accuracy of defect detection at multiple scales. Meanwhile, the Spatial Detail Extraction Module (SDEM) is added to the decoding network, which helps to retain the spatial detail information in the decoding process and further improves the detection accuracy of small-scale defects. The experimental results show that the mean accuracy of the semantic segmentation of the method proposed in this paper can reach 90.1%, the mean dice coefficient can reach 89.5%, and the segmentation speed can reach 37.83 FPS, which is higher than other networks’ segmentation accuracy. And, at the same time, it can achieve higher efficiency. Full article
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<p>Rail-STrans network framework.</p>
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<p>Rail surface defect image from the RSDDs dataset.</p>
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<p>Dataset built in this paper. (<b>a</b>) Original picture. (<b>b</b>) Flip 45 degrees. (<b>c</b>) Flip horizontal. (<b>d</b>) Flip vertical.</p>
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<p>Dataset built in this paper. (<b>a</b>) Original picture. (<b>b</b>) Flip 45 degrees. (<b>c</b>) Flip horizontal. (<b>d</b>) Flip vertical.</p>
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<p>Improved Swin Transformer network structure diagram.</p>
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<p>LPM framework.</p>
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<p>The architecture of the Swin Transformer block.</p>
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<p>The architecture of MFFM.</p>
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<p>The architecture of SDEM. (<b>a</b>) SDEM; (<b>b</b>) the structure of DM.</p>
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<p>Confusion matrix.</p>
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<p>Frames for railroad inspection car.</p>
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<p>The training curve of loss function.</p>
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<p>Partial picture display of ablation experiments. (<b>a</b>) Original picture; (<b>b</b>) swin_upernet; (<b>c</b>) swin_upernet + LPM; (<b>d</b>) Swin Transformer + SDEM; (<b>e</b>) Swin Transformer + MFFM; (<b>f</b>) Swin Transformer + LPM + SDEM; (<b>g</b>) Swin Transformer + MFFM + SDEM; (<b>h</b>) Swin Transformer + LPM + MFFM; (<b>i</b>) Rail-STrans.</p>
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<p>Partial picture display of ablation experiments. (<b>a</b>) Original picture; (<b>b</b>) swin_upernet; (<b>c</b>) swin_upernet + LPM; (<b>d</b>) Swin Transformer + SDEM; (<b>e</b>) Swin Transformer + MFFM; (<b>f</b>) Swin Transformer + LPM + SDEM; (<b>g</b>) Swin Transformer + MFFM + SDEM; (<b>h</b>) Swin Transformer + LPM + MFFM; (<b>i</b>) Rail-STrans.</p>
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<p>Performance comparison of different segmentation models.</p>
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<p>The visual segmentation results of different models. (<b>a</b>) Original picture; (<b>b</b>) deeplabV3+; (<b>c</b>) segnext_mscan; (<b>d</b>) U-Net; (<b>e</b>) swin_upernet; (<b>f</b>) SegFormer; (<b>g</b>) Mask R-CNN+; (<b>h</b>) Rail-STrans.</p>
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18 pages, 3537 KiB  
Article
Characterization and Transcriptome Analysis Reveal Exogenous GA3 Inhibited Rosette Branching via Altering Auxin Approach in Flowering Chinese Cabbage
by Xinghua Qi, Ying Zhao, Ningning Cai, Jian Guan, Zeji Liu, Zhiyong Liu, Hui Feng and Yun Zhang
Agronomy 2024, 14(4), 762; https://doi.org/10.3390/agronomy14040762 - 8 Apr 2024
Cited by 1 | Viewed by 1115
Abstract
Branching is an important agronomic trait that is conducive to plant architecture and yield in flowering Chinese cabbage. Plant branching is regulated by a complex network mediated by hormones; gibberellin (GA) is one of the important hormones which is involved in the formation [...] Read more.
Branching is an important agronomic trait that is conducive to plant architecture and yield in flowering Chinese cabbage. Plant branching is regulated by a complex network mediated by hormones; gibberellin (GA) is one of the important hormones which is involved in the formation of shoot branching. Research on the regulatory mechanism of GA influencing rosette branch numbers is limited for flowering Chinese cabbage. In this study, the exogenous application of 600 mg/L GA3 effectively inhibited rosette branching and promoted internode elongation in flowering Chinese cabbage. RNA-Seq analysis further found that these DEGs were significantly enriched in ‘the plant hormone signal transduction’ pathways, and auxin-related genes were significantly differentially expressed between MB and MB_GA. The upregulation of auxin (AUX) and the upregulation of auxin/indole-3-acetic acid (AUX/IAA), as well as the downregulation of SMALL AUXIN-UPREGULATED RNA (SAUR), were found in the negative regulation of the rosette branching. The qRT-PCR results showed that the expression of AUX/IAA and SAUR from IAA gene family members were consistent with the results of transcriptome data. Phytohormone profiling by targeted metabolism revealed that endogenous auxin contents were significantly increased in MB_GA. Transcriptome and metabolome analysis clarified the main plant hormones and genes underlying the rosette branching in flowering Chinese cabbage, confirming that auxin could inhibit rosette branching. In this regard, the results present a novel angle for revealing the mechanism of gibberellin acting on the branching architecture in flowering Chinese cabbage. Full article
(This article belongs to the Special Issue Advances in Crop Molecular Breeding and Genetics)
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<p>Phenotypes of MB and MB with 600 mg/L of GA<sub>3</sub> treatment. The entire plant appearance of MB (<b>A</b>) and MB after 600 mg/L of GA<sub>3</sub> treatment (<b>B</b>). The phenotype of rosette branching in MB (<b>C</b>) and MB after 600 mg/L of GA<sub>3</sub> treatment (<b>D</b>). The rosette branching is indicated with red arrows.</p>
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<p>The primary rosette branch numbers of MB and MB_GA (<b>A</b>). Relationship between internode position and internode length (<b>B</b>). * and ** indicate significant differences in expression levels at <span class="html-italic">p</span> &lt; 0.05 and <span class="html-italic">p</span> &lt; 0.01 between the two types as determined according to the <span class="html-italic">t</span>-test.</p>
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<p>Comparative analysis of expression patterns of differentially expressed genes (DEGs) in six segments of MB. Hierarchical cluster diagram of gene expression level in samples. MB1, MB2, and MB3 are controls; MB_GA_1, MB_GA_2, and MB_GA_3 are the experimental groups treated with 600 mg/L GA<sub>3</sub> (<b>A)</b>. Principal component analysis (PCA) of the differentially expressed genes between MB and MB_GA (<b>B</b>). Volcano plot of the differentially expressed genes between MB and MB_GA. Blue indicates downregulation of the gene, red indicates upregulation of the gene, and gray indicates non−regulation of the gene (<b>C</b>). The number of up− and down−regulated expressed genes (<b>D</b>).</p>
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<p>The trend analysis of the expression profile of all DEGs in all six pairwise comparisons. The <span class="html-italic">y</span>-axis represents the clustering groups of the gene expression level and the <span class="html-italic">x</span>-axis represents the different samples.</p>
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<p>Twenty most significantly enriched GO and KEGG metabolic pathways. (<b>A</b>) GO enrichment analysis for MB vs. MB_GA; (<b>B</b>) KEGG enrichment analysis for MB vs. MB_GA.</p>
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<p>Expression of differentially expressed genes involved in the plant hormone genes (auxin, cytokinin, abscisic acid). Note: The bar on the right represents the relative expression values. Upregulated genes are marked with red borders and downregulated genes with green borders. Unchanged genes are marked with black borders (<b>A</b>). Expression of differentially expressed genes involved in the plant hormone genes (gibberellin, ethylene, brassinosteroid, jasmonic acid) (<b>B</b>).</p>
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<p>Expression profiles of 11 key differentially expressed genes (DEGs) in the MB and MB_GA. Error bars represent the standard error of the mean for three biological replicates. ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001 determined by Student’s <span class="html-italic">t</span>-test.</p>
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<p>Determination of the content of auxin in MB and MB_GA. ** <span class="html-italic">p</span> &lt; 0.01 determined by Student’s <span class="html-italic">t</span>-test.</p>
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<p>A hypothetical regulatory network of the rosette branching inhibited by exogenous GA<sub>3</sub> in flowering Chinese cabbage.</p>
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