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16 pages, 1798 KiB  
Article
Evaluation of Evapotranspiration Prediction for Cassava Crop Using Artificial Neural Network Models and Empirical Models over Cross River Basin in Nigeria
by Oluwadamilare Oluwasegun Eludire, Oluwaseun Temitope Faloye, Michael Alatise, Ayodele Ebenezer Ajayi, Philip Oguntunde, Tayo Badmus, Abayomi Fashina, Oluwafemi E. Adeyeri, Idowu Ezekiel Olorunfemi and Akinwale T. Ogunrinde
Water 2025, 17(1), 87; https://doi.org/10.3390/w17010087 - 1 Jan 2025
Viewed by 345
Abstract
The accurate assessment of water availability throughout the cassava cropping season (the initial, developmental, mid-season, and late stages) is crucial for mitigating the impacts of climate change on crop production. Using the Mann–Kendall Test, we investigated the trends in rainfall and cassava crop [...] Read more.
The accurate assessment of water availability throughout the cassava cropping season (the initial, developmental, mid-season, and late stages) is crucial for mitigating the impacts of climate change on crop production. Using the Mann–Kendall Test, we investigated the trends in rainfall and cassava crop evapotranspiration (ETc) within the Cross River basin in Nigeria. Reference evapotranspiration (ETo) was based on two approaches, namely Artificial Neural Network (ANN) modelling and three established empirical models—the Penman–Monteith (considered the standard method), Blaney–Morin–Nigeria (BMN), and Hargreaves–Samani (HAG) models. ANN predictions were performed by using inputs from BMN and HAG parameters, denoted as BMN-ANN and HAG-ANN, respectively. The results from the ANN models were compared to those obtained from the Penman–Monteith method. Remotely sensed meteorological data spanning 39 years (1979–2017) were acquired from the Climatic Research Unit (CRU) to estimate ETc, while cassava yield data were acquired from the International Institute of Tropical Agriculture (IITA), Ibadan. The study revealed a significant upward trend in cassava crop ETc over the study period. Additionally, the ANN models outperformed the empirical models in terms of prediction accuracy. The BMN-ANN model with a Tansig activation function and a 3-3-1 architecture (number of input neurons, hidden layers, and output neurons) achieved the highest performance, with a coefficient of determination (R2) of 0.9890, a root mean square error (RMSE) of 0.000056 mm/day, and a Willmott’s index of agreement (d) of 0.9960. There is a decreasing trend in cassava yield in the region and further analysis indicated potential average daily water deficits of approximately −1.1 mm/day during the developmental stage. These deficits could potentially hinder root biomass, yield, and overall cassava yield in the Cross River basin. Our findings highlight the effectiveness of ANN modelling for irrigation planning, especially in the face of a worsening climate change scenario. Full article
(This article belongs to the Special Issue Crop Evapotranspiration, Crop Irrigation and Water Savings)
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Figure 1
<p>Map of Nigeria showing the Cross River basin, showing the 22 stations used by ArcGIS Pro 3.1.</p>
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<p>Network architecture showing input, hidden, and output layer connections.</p>
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<p>Annual trend in cassava cropping seasonal rainfall.</p>
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<p>Annual yield of cassava over Cross River basin from IITA yield data.</p>
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<p>Neural network structure of BMN-LogSig-ANN-3-1-1.</p>
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16 pages, 8192 KiB  
Article
Improved CSW-YOLO Model for Bitter Melon Phenotype Detection
by Haobin Xu, Xianhua Zhang, Weilin Shen, Zhiqiang Lin, Shuang Liu, Qi Jia, Honglong Li, Jingyuan Zheng and Fenglin Zhong
Plants 2024, 13(23), 3329; https://doi.org/10.3390/plants13233329 - 27 Nov 2024
Viewed by 486
Abstract
As a crop with significant medicinal value and nutritional components, the market demand for bitter melon continues to grow. The diversity of bitter melon shapes has a direct impact on its market acceptance and consumer preferences, making precise identification of bitter melon germplasm [...] Read more.
As a crop with significant medicinal value and nutritional components, the market demand for bitter melon continues to grow. The diversity of bitter melon shapes has a direct impact on its market acceptance and consumer preferences, making precise identification of bitter melon germplasm resources crucial for breeding work. To address the limitations of time-consuming and less accurate traditional manual identification methods, there is a need to enhance the automation and intelligence of bitter melon phenotype detection. This study developed a bitter melon phenotype detection model named CSW-YOLO. By incorporating the ConvNeXt V2 module to replace the backbone network of YOLOv8, the model’s focus on critical target features is enhanced. Additionally, the SimAM attention mechanism was introduced to compute attention weights for neurons without increasing the parameter count, further enhancing the model’s recognition accuracy. Finally, WIoUv3 was introduced as the bounding box loss function to improve the model’s convergence speed and positioning capabilities. The model was trained and tested on a bitter melon image dataset, achieving a precision of 94.6%, a recall of 80.6%, a mAP50 of 96.7%, and an F1 score of 87.04%. These results represent improvements of 8.5%, 0.4%, 11.1%, and 4% in precision, recall, mAP50, and F1 score, respectively, over the original YOLOv8 model. Furthermore, the effectiveness of the improvements was validated through heatmap analysis and ablation experiments, demonstrating that the CSW-YOLO model can more accurately focus on target features, reduce false detection rates, and enhance generalization capabilities. Comparative tests with various mainstream deep learning models also proved the superior performance of CSW-YOLO in bitter melon phenotype detection tasks. This research provides an accurate and reliable method for bitter melon phenotype identification and also offers technical support for the visual detection technologies of other agricultural products. Full article
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<p>Bitter gourd images in different states: (<b>a</b>) before harvesting, (<b>b</b>) after harvesting.</p>
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<p>Effects of image enhancement. (<b>a</b>) Original image, (<b>b</b>) vertical flip, (<b>c</b>) mirror flip + brightness increase, (<b>d</b>) combination of multiple methods.</p>
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<p>Improved network structure.</p>
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<p>FCMAE: fully convolutional masked autoencoder.</p>
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<p>ConvNeXt block designs.</p>
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<p>Schematic of the SimAM attention mechanism.</p>
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<p>Schematic of anchor boxes and target boxes.</p>
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<p>Performance comparison before and after network improvements.</p>
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<p>Heatmaps before and after network improvement. (<b>a</b>) Original image, (<b>b</b>) before improvement, (<b>c</b>) after improvement.</p>
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<p>Discrimination results of different models.</p>
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22 pages, 9450 KiB  
Article
Neonicotinoid Pesticides Affect Developing Neurons in Experimental Mouse Models and in Human Induced Pluripotent Stem Cell (iPSC)-Derived Neural Cultures and Organoids
by Alessandro Mariani, Davide Comolli, Roberto Fanelli, Gianluigi Forloni and Massimiliano De Paola
Cells 2024, 13(15), 1295; https://doi.org/10.3390/cells13151295 - 31 Jul 2024
Cited by 1 | Viewed by 1285
Abstract
Neonicotinoids are synthetic, nicotine-derived insecticides used worldwide to protect crops and domestic animals from pest insects. The reported evidence shows that they are also able to interact with mammalian nicotine receptors (nAChRs), triggering detrimental responses in cultured neurons. Exposure to high neonicotinoid levels [...] Read more.
Neonicotinoids are synthetic, nicotine-derived insecticides used worldwide to protect crops and domestic animals from pest insects. The reported evidence shows that they are also able to interact with mammalian nicotine receptors (nAChRs), triggering detrimental responses in cultured neurons. Exposure to high neonicotinoid levels during the fetal period induces neurotoxicity in animal models. Considering the persistent exposure to these insecticides and the key role of nAChRs in brain development, their potential neurotoxicity on mammal central nervous system (CNS) needs further investigations. We studied here the neurodevelopmental effects of different generations of neonicotinoids on CNS cells in mouse fetal brain and primary cultures and in neuronal cells and organoids obtained from human induced pluripotent stem cells (iPSC). Neonicotinoids significantly affect neuron viability, with imidacloprid (IMI) inducing relevant alterations in synaptic protein expression, neurofilament structures, and microglia activation in vitro, and in the brain of prenatally exposed mouse fetuses. IMI induces neurotoxic effects also on developing human iPSC-derived neurons and cortical organoids. Collectively, the current findings show that neonicotinoids might induce impairment during neuro/immune-development in mouse and human CNS cells and provide new insights in the characterization of risk for the exposure to this class of pesticides. Full article
(This article belongs to the Section Cells of the Nervous System)
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Figure 1
<p>Expression of α7-nAChR in cultured neurons and glia. Primary neuron/glia cocultures obtained from different areas of mouse embryo brain were immunostained for NF200 (<b>A</b>,<b>D</b>,<b>G</b>; green), CD11b (<b>J</b>) or GFAP (<b>M</b>), and α7-nAChR (<b>B</b>,<b>E</b>,<b>H</b>,<b>K</b>,<b>N</b>; red) at 14 DIV. Images were acquired by a confocal microscope at 400× magnification, scale bars 50 µm. Neurons derived from different brain areas showed a widespread α7-nAChR distribution colocalizing with NF200-positive cells (<b>C</b>,<b>F</b>,<b>I</b>; merge). CD11b-positive microglia (<b>J</b>) also expressed α7-nAChR (<b>K</b>, red) as shown by colocalized signals in the merge picture (<b>L</b>). A very weak non-specific α7-nAChR signal (<b>N</b>,<b>O</b>) was detected for GFAP-positive astrocytes (<b>M</b>).</p>
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<p>Effects of neonicotinoids on neuron viability. Primary neuronal, cultures obtained from different mouse embryo brain areas (HN: hippocampal neurons, CBN: cerebellar neurons, CXN: cortical neurons) were treated with different concentrations of neonics (up to 10,000× aFBC) or comparable doses of nicotine at 3 DIV (<b>A</b>–<b>D</b>) or 13 DIV (<b>E</b>–<b>H</b>) for 72 h. Neuron viability was evaluated from 3 independent experiments via MTS 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, **** <span class="html-italic">p</span> &lt; 0.0001 versus control. Two-way ANOVA and Dunnett’s post-test.</p>
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<p>Dose–response effects of mecamylamine. Hippocampal cultures were treated with the mecamylamine for 72 h (from 1 nM up to 6.2 mM). **** <span class="html-italic">p</span> &lt; 0.0001 versus control. Data are expressed as mean ± st.dev of 3 replicates/conditions from 3 independent experiments. One-way ANOVA and Dunnett’s post-test. The LC50, LOAEL, and NOAEL were calculated using GraphPad Prism software 6.01 (logarithmic transformation of X-values and non-linear regression, sigmoidal dose–response analysis with variable slope, with bottom and top constrains set at 0 and 100, respectively).</p>
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<p>Mecamylamine reverts imidacloprid- and nicotine-induced neurotoxic effects. Primary hippocampal neurons were cotreated with 10 μM mecamylamine and 50 μM imidacloprid or nicotine (NIC) at 13 DIV for 72 h. Neuron viability was evaluated via MTS test. Data are from 3 independent experiments (N = 18). ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05 versus control; ° <span class="html-italic">p</span> &lt; 0.05, °°°° <span class="html-italic">p</span> &lt; 0.0001 vs. treatment with imidacloprid or nicotine alone, respectively. F<sub>interaction</sub> (2.102) = 6.23; <span class="html-italic">p</span> &lt; 0.01. Two-way ANOVA and Tukey’s post-test.</p>
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<p>Neonicotinoid effects on microglia inflammatory response. Neonic effects on microglia activation and their responses to a pro-inflammatory stimulus (1 μg/mL LPS) were evaluated with in purified cultures treated with imidacloprid (up to 1000× aFBC, 170 μM) for 72 h. (<b>A</b>) Quantification of the expression levels of mRNA related to M1 (TNFα) or M2 (YM1) phenotype markers (by RT-PCR). The exposure to imidacloprid did not induce alterations in TNFα and YM1 mRNA. (<b>B</b>) LPS treatment induced TNFα expression, which was significantly inhibited by pre-incubation with imidacloprid (170 μM). (<b>C</b>) IMI significantly reduced the TNFα release in conditioned media in LPS-stimulated microglia cultures, as measured by ELISA assay. Data were obtained from 3-6 independent experiments. ° <span class="html-italic">p</span> &lt; 0.05; °°° <span class="html-italic">p</span> &lt; 0.001 versus 1 μg/mL LPS. One-way ANOVA and Dunnett’s post-test.</p>
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<p>Imidacloprid induced neurodevelopmental alterations in cultured neurons. The in vitro effects of imidacloprid on immature neurofilaments and presynaptic protein (synaptophysin) expression and on dendritic arborization were analyzed in hippocampal “sandwich” cocultures treated with the insecticide for 72 h at 13 DIV. Cells were stained with DCX, NF200, and synaptophysin antibodies; nuclei were counterstained with Hoechst 33258 dye (blue). Three-dimensional neuron reconstruction was then performed, and the different marker expressions were analyzed. (<b>A</b>) As an index of neuron maturation, the ratio between DCX (green) and NF200 (red) volumes was quantified. Exposure to imidacloprid (up to 17 μM, 100× aFBC) did not significantly affect the DCX/NF200 ratio. (<b>B</b>) Automated Sholl analyses, for detecting alterations in neuron branching complexity, were performed on the acquired images (NF200 in red). IMI reduced the number of dendritic branches per neuron from the lower tested concentration (170 nM). (<b>C</b>) The number of synaptophysin-positive puncta (green) were determined and normalized for NF200 (red) volume. * <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 versus control; one-way ANOVA and Dunnett’s post-test. At least 5 fields (600×) for each condition were analyzed from three independent experiments.</p>
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<p>α7-nAChR expression in human iPSC-derived neurons and astrocytes. iPSC-derived neurons (i-neu) and astrocytes (i-astro) were differentiated from NPCs for 28 DIV. Immunocytochemistry was performed on differentiated cells using neuron (NF200; <b>A</b>, green)- or astrocyte (S100β; <b>D</b>, green)- and α7-nAChR (<b>B</b>,<b>E</b>, red)-specific antibodies. Images were acquired via a confocal microscope at 400x magnification, scale bars 50 µm. Mature i-neu (<b>A</b>–<b>C</b>) and i-astro (<b>D</b>–<b>F</b>) showed a widespread α7-nAChR distribution colocalizing with NF200-positive (<b>C</b>, merged signal) or S100β-positive (<b>F</b>, merged signal) cells.</p>
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<p>Human iPSC-derived neuron and astrocyte viability is affected by imidacloprid in specific developmental stages. (<b>A</b>–<b>E</b>) I-neu were exposed to IMI by repetitive treatments with different pesticide concentrations, from 3 to 28 DIV of differentiation. Cell viability was evaluated with MTT assay at different time points: 3 (<b>A</b>), 10 (<b>B</b>), 14 (<b>C</b>), 21 (<b>D</b>) and 28 (<b>E</b>) DIV. (<b>F</b>) I-astro were differentiated for 28 days, then treated with IMI for 72h. Cell death was quantified via LDH release assay. Data were obtained from 3-10 replicates in 3 independent experiments. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 versus untreated cultures. One-way ANOVA and Dunnett’s post-test.</p>
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<p>Chronic exposure to imidacloprid induces cell death in human iPSC-derived cortical organoids. Representative image of mature hCO stained for nuclei (blue), astrocytes (green), and neurons (red) showing cell interaction complexity (merge). hCOs obtained from confluent NPCs were cultured for 60 DIV and treated with 5 nM or 17 μM IMI (eFBC and aFBC, respectively) three times a week starting from 11 DIV. Conditioned media were collected before the treatment (0 DIV) and at 25, 35 49, and 60 DIV, and LDH release was measured at the different time points. An amount of 17 μM IMI induced an increase in LDH release at 25, 35, and 60 DIV compared to untreated cultures. No significant effects were revealed for 5 nM IMI. Data were obtained from 3–15 replicates for each time point. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001 versus untreated cultures, ° <span class="html-italic">p</span> &lt; 0.05 versus 5 nM IMI. One-way ANOVA and Dunnett’s post-test at each time point.</p>
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<p>Prenatal exposure to imidacloprid or nicotine induced synaptic alterations in the hippocampus and cerebellum of newborn mice. The effects of prenatal exposure to imidacloprid on synaptic protein expression were evaluated by immunohistochemical analyses performed on single brains isolated from prenatally exposed (up to 10× ADI for imidacloprid) newborn mice of at least three different litters. (<b>A</b>) Representative images of synaptophysin staining in hippocampus and cerebellum of control and imidacloprid-treated mouse brains. Scale bar, 250 µm. (<b>B</b>) Quantification of the integrated density of synaptophysin staining in the hippocampus (left) and cerebellum (right). Imidacloprid increased synaptophysin expression starting from ADI. Nicotine induced an increase in synaptophysin expression already at the lower dose (<span class="html-italic">p</span> &lt; 0.05 compared to control group) only in the hippocampus. Data obtained from at least 3 different litters from 3 independent experiments. * <span class="html-italic">p</span> &lt; 0.05; *** <span class="html-italic">p</span> &lt; 0.001 versus control group; one-way ANOVA and Dunnett’s post-test.</p>
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<p>Prenatal exposure to imidacloprid or nicotine induced impairments in doublecortin expression in the hippocampus and cerebellum of newborn mice. The effects of prenatal exposure to imidacloprid and nicotine on doublecortin expression were evaluated by immunohistochemical analyses performed on single brains isolated from prenatally exposed newborn mice (up to 10× ADI for imidacloprid) of at least three different litters. (<b>A</b>) Representative images of DCX fluorescent signal (green: nuclei in blue) in hippocampus and cerebellum of control and imidacloprid-treated mouse brains. Scale bar, 200 µm. (<b>B</b>) Quantification of the area stained by DCX antibody on the total area analyzed in the hippocampus (left) and cerebellum (right). Data obtained from at least 3 different litters from 3 independent experiments. * <span class="html-italic">p</span> &lt; 0.05 versus control group; one-way ANOVA and Dunnett’s post-test.</p>
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<p>Prenatal exposure to imidacloprid or nicotine induced microglial alterations in the hippocampus and cerebellum of newborn mice. The effects of prenatal exposure to imidacloprid and nicotine on microglial markers (IBA-1 or CD11b) were evaluated by immunohistochemical analyses performed on single brains isolated from prenatally exposed newborn mice (up to 10× ADI for imidacloprid) from at least three different litters. (<b>A</b>) Representative images of IBA-1-positive cells in hippocampus and cerebellum of control and imidacloprid-treated mouse brains. Scale bar, 500 µm for the hippocampus and 300 µm for the cerebellum. (<b>B</b>) Quantification of the density of IBA-1-positive cells (n cells/mm<sup>2</sup>) in the hippocampus (left) and cerebellum (right). Data obtained from at least 3 different litters from 3 independent experiments. * <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 versus control group; one-way ANOVA and Dunnett’s post-test.</p>
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<p>Overall experimental design of this study is reported.</p>
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15 pages, 4429 KiB  
Article
The Effect of Biotic Stress in Plant Species Induced by ‘Candidatus Phytoplasma solani’—An Artificial Neural Network Approach
by Ivica Djalovic, Petar Mitrovic, Goran Trivan, Aleksandra Jelušić, Lato Pezo, Elizabet Janić Hajnal and Tatjana Popović Milovanović
Horticulturae 2024, 10(5), 426; https://doi.org/10.3390/horticulturae10050426 - 23 Apr 2024
Viewed by 1320
Abstract
Infections with phytoplasma present one of the most significant biotic stresses influencing plant health, growth, and production. The phytoplasma ‘Candidatus Phytoplasma solani’ infects a variety of plant species. This pathogen impacts the physiological and morphological characteristics of plants causing stunting, yellowing, leaf [...] Read more.
Infections with phytoplasma present one of the most significant biotic stresses influencing plant health, growth, and production. The phytoplasma ‘Candidatus Phytoplasma solani’ infects a variety of plant species. This pathogen impacts the physiological and morphological characteristics of plants causing stunting, yellowing, leaf curling, and other symptoms that can lead to significant economic losses. The aim of this study was to determine biochemical changes in peony (Paeonia tenuifolia L.), mint (Mentha × piperita L.), and dill (Anethum graveolens L.) induced by ‘Ca. Phytoplasma solani’ in Serbia as well as to predict the impact of the biotic stress using artificial neural network (ANN) modeling. The phylogenetic position of the Serbian ‘Ca. Phytoplasma solani’ strains originated from the tested hosts using 16S rRNA (peony and carrot strains) and plsC (mint and dill strains) sequences indicated by their genetic homogeneity despite the host of origin. Biochemical parameters significantly differed in asymptomatic and symptomatic plants, except for total anthocyanidins contents in dill and the capacity of peony and mint extracts to neutralize superoxide anions and hydroxyl radicals, respectively. Principal Component Analysis (PCA) showed a correlation between different chemical parameters and revealed a clear separation among the samples. Based on the ANN performance, the optimal number of hidden neurons for the calculation of TS, RG, PAL, LP, NBT, OH, TP, TT, Tflav, Tpro, Tant, DPPH, and Car was nine (using MLP 8-9-13), as it produced high r2 values (1.000 during the training period) and low SOS values. Developing an effective early warning system for the detection of plant diseases in different plant species is critical for improving crop yield and quality. Full article
(This article belongs to the Special Issue The Diagnosis, Management, and Epidemiology of Plant Diseases)
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<p>Symptoms caused by ‘<span class="html-italic">Ca</span>. Phytoplasma solani’ on (<b>A</b>) peony<span class="html-italic">—P. tenuifolia</span>, (<b>B</b>) dill—<span class="html-italic">A. graveolens</span>, (<b>C</b>) mint<span class="html-italic">—Mentha</span> × <span class="html-italic">piperita</span>, and (<b>D</b>) carrot<span class="html-italic">—D. carota</span>.</p>
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<p>ANN topology with three layers (input, output, and hidden) with weights, biases, and transfer functions.</p>
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<p>Neighbor-joining phylogenetic tree showing the position of the three tested Serbian ‘<span class="html-italic">Ca</span>. Phytoplasma solani’ strains from <span class="html-italic">P. tenuifolia</span> <span class="html-fig-inline" id="horticulturae-10-00426-i001"><img alt="Horticulturae 10 00426 i001" src="/horticulturae/horticulturae-10-00426/article_deploy/html/images/horticulturae-10-00426-i001.png"/></span> and <span class="html-italic">D. carota</span> <span class="html-fig-inline" id="horticulturae-10-00426-i002"><img alt="Horticulturae 10 00426 i002" src="/horticulturae/horticulturae-10-00426/article_deploy/html/images/horticulturae-10-00426-i002.png"/></span> and 23 comparative <span class="html-italic">Phytoplasma</span> spp. strains belonging to different 16Sr Groups. <span class="html-italic">Acholeplasma laidlawii</span> strain NCTC10116 from the GenBank database served as an outgroup.</p>
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<p>Neighbor-joining phylogenetic tree showing the position of the two tested Serbian ‘<span class="html-italic">Ca</span>. Phytoplasma solani’ strains from <span class="html-italic">A. graveolens</span> <span class="html-fig-inline" id="horticulturae-10-00426-i003"><img alt="Horticulturae 10 00426 i003" src="/horticulturae/horticulturae-10-00426/article_deploy/html/images/horticulturae-10-00426-i003.png"/></span> and <span class="html-italic">Mentha</span> × <span class="html-italic">piperita</span> <span class="html-fig-inline" id="horticulturae-10-00426-i004"><img alt="Horticulturae 10 00426 i004" src="/horticulturae/horticulturae-10-00426/article_deploy/html/images/horticulturae-10-00426-i004.png"/></span> and 13 comparative <span class="html-italic">Phytoplasma</span> spp. strains according to sequences of the <span class="html-italic">plsC</span> gene. <span class="html-italic">Acholeplasma laidlawii</span> strain DSM23060 from the GenBank database served as an outgroup.</p>
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<p>Biplot graph of chemical analysis for asymptomatic (A) and symptomatic (S) samples of the leaves of peony, mint, dill, and carrot.</p>
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<p>The relative influence of plant type and treatment on (<b>a</b>) TS, (<b>b</b>) RG, (<b>c</b>) PAL, (<b>d</b>) LP, (<b>e</b>) ATO2, (<b>f</b>) ATOH, (<b>g</b>) TP, (<b>h</b>) TT, (<b>i</b>) Tflav, (<b>j</b>) Tpro, (<b>k</b>) Tant, (<b>l</b>) DPPH, (<b>m</b>) Car, (<b>n</b>) Tcha, and (<b>o</b>) Tchb.</p>
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18 pages, 4602 KiB  
Article
Exposure of Zebrafish Embryos to Urea Affects NOS1 Gene Expression in Neuronal Cells
by Pietro Cacialli, Serena Ricci, Flavia Frabetti, Sara Ferrando and Valeria Franceschini
Environments 2024, 11(3), 41; https://doi.org/10.3390/environments11030041 - 21 Feb 2024
Cited by 3 | Viewed by 2265
Abstract
Nitrogen-based fertilizers represent the most common fertilization tools, particularly used in crop food agriculture, despite the low cost-efficiency and the high negative environmental impact. At present, there is still inadequate information available about the effects of urea on human health; nevertheless, previous studies [...] Read more.
Nitrogen-based fertilizers represent the most common fertilization tools, particularly used in crop food agriculture, despite the low cost-efficiency and the high negative environmental impact. At present, there is still inadequate information available about the effects of urea on human health; nevertheless, previous studies in animals observed that high urea concentration exposure can damage different tissues, including the brain. In several vertebrates, a crucial factor involved in neuronal cell formation is represented by the gas molecule, nitric oxide (NO), derived from the conversion of arginine to citrulline through the enzymatic activity of nitric oxide synthases (NOS). In zebrafish, three different isoforms of the NOS gene are known: nos1, nos2a, and nos2b. In the present study we show that nos1 represents the unique isoform with a stable high expression in the brain and spinal cord during all the embryonic stages of zebrafish development. Then, by using a specific transgenic zebrafish line, Tg(HuC:GFP), to mark neuronal cells, we observed nos1 to be specifically expressed in neurons. Interestingly, we observed that urea exposure at sub-lethal doses affected cell proliferation and the number of nos1-expressing cells, inducing apoptosis. Consistently, brain NO levels were observed to be reduced in urea-treated animals compared to untreated ones. This finding represents the first evidence that urea exposure affects the expression of a key gene involved in neuronal cell formation during embryonic development. Full article
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Figure 1
<p>Analysis of <span class="html-italic">NOS</span> gene expression by qPCR. (<b>a</b>) Experimental outline of qPCR experiments at different stages of embryonic brain development (24; 48; 72 and 96 hpf). A pool of 30 heads was used for each group. (<b>b</b>) qPCR analysis of <span class="html-italic">NOS</span> gene family: <span class="html-italic">nos1</span>, <span class="html-italic">nos2a</span>, and <span class="html-italic">nos2b</span>. The gene, <span class="html-italic">nos1</span>, was the most expressed during brain development in zebrafish embryos, compared to <span class="html-italic">nos2a</span> and <span class="html-italic">nos2b</span> (** <span class="html-italic">p</span> &lt; 0.001; *** <span class="html-italic">p</span> &lt; 0.0001; ns: not-significant). All results are represented as the means ± SD of three independent experiments.</p>
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<p>Whole-mount in situ hybridization and chromogenic revelation for <span class="html-italic">nos1</span>, <span class="html-italic">nos2a</span>, and <span class="html-italic">nos2b</span> genes at different stages of zebrafish embryonic development (24, 48, 72, and 96 hpf). Expression of <span class="html-italic">nos1</span> is high in the brain and eyes at all stages of development.</p>
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<p>Fluorescence whole-mount in situ hybridization for <span class="html-italic">nos1</span> combined with immunohistochemistry to detect anti-GFP in <span class="html-italic">HuC:GFP</span> embryos at 30 hpf. (<b>a</b>) Fluorescence WISH for <span class="html-italic">nos1</span>, rectangles indicate respectively head and spinal cord. (<b>b</b>) Fluorescence WISH for <span class="html-italic">nos1</span> (red), combined with immunohistochemistry to detect anti-GFP (green) in the heads of <span class="html-italic">HuC:GFP</span> embryos. (<b>c</b>) Fluorescence WISH for <span class="html-italic">nos1</span> (red), combined with immunohistochemistry to detect anti-GFP (green) in the spinal cord of <span class="html-italic">HuC:GFP</span> embryos, with zoom of spinal cord region (within the rectangle box, white arrows indicate co-expressed cells).</p>
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<p>(<b>a</b>) Experimental outline of urea treatment in zebrafish embryos. (<b>b</b>) Survival rate of zebrafish embryos (40 embryos per group) treated with different concentrations of urea (0, 10, 50, 100 mM).</p>
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<p>Morphological evaluation at 24 hpf of zebrafish embryos having undergone urea exposure (0, 10, 50, 100 mM).</p>
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<p>Fluorescence WISH for <span class="html-italic">nos1</span> and DAPI (to mark cell nuclei) in control and urea-treated embryos (dorsal view of head).</p>
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<p>(<b>a</b>) Fluorescence WISH for <span class="html-italic">nos1</span> and DAPI in control and urea-treated embryos at 48 hpf (dorsal view of head). (<b>b</b>) Fluorescence WISH for <span class="html-italic">nos1</span> and DAPI in control and urea-treated embryos at 72 hpf (dorsal view of head).</p>
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<p>Fluorescence WISH for <span class="html-italic">nos1</span> and DAPI in control and urea-treated embryos at 96 hpf (dorsal view of head).</p>
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<p>(<b>a</b>) Fluorescence ISH for <span class="html-italic">nos1</span>, TUNEL staining and DAPI in control and urea-treated embryos at 96 hpf (paraffin section of brain from embryos). (<b>b</b>) Statistical analysis (unpaired <span class="html-italic">t</span> test) of <span class="html-italic">nos1</span>-expressing cell number was calculated based on average of three paraffin sections obtained from 10 urea-treated heads and 10 non-treated heads (** <span class="html-italic">p</span> &lt; 0.001). (<b>c</b>) Statistical analysis (unpaired <span class="html-italic">t</span> test) of TUNEL positive cell number was calculated based on average of three paraffin sections obtained from 10 urea-treated heads and 10 non-treated heads (*** <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>(<b>a</b>) NO production was detected at 96 hpf after urea treatment and/or supplementation with LPS (to stimulate NO production). The intracellular NO production levels were observed via a fluorescence microscope after staining with diamino fluorophore DAF-FM DA. (<b>b</b>) Relative fluorescence intensity. All results are represented as the means ± SD of three independent experiments. Statistical analysis was performed by one-way ANOVA (multiple comparison—Tukey–Kramer post hoc test) using calculations from a total of 15 embryos (** <span class="html-italic">p</span> &lt; 0.001; *** <span class="html-italic">p</span> &lt; 0.0001; ns: not significant).</p>
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17 pages, 13020 KiB  
Article
A Fractional-Order Memristive Two-Neuron-Based Hopfield Neuron Network: Dynamical Analysis and Application for Image Encryption
by Jayaraman Venkatesh, Alexander N. Pchelintsev, Anitha Karthikeyan, Fatemeh Parastesh and Sajad Jafari
Mathematics 2023, 11(21), 4470; https://doi.org/10.3390/math11214470 - 28 Oct 2023
Cited by 7 | Viewed by 1282
Abstract
This paper presents a study on a memristive two-neuron-based Hopfield neural network with fractional-order derivatives. The equilibrium points of the system are identified, and their stability is analyzed. Bifurcation diagrams are obtained by varying the magnetic induction strength and the fractional-order derivative, revealing [...] Read more.
This paper presents a study on a memristive two-neuron-based Hopfield neural network with fractional-order derivatives. The equilibrium points of the system are identified, and their stability is analyzed. Bifurcation diagrams are obtained by varying the magnetic induction strength and the fractional-order derivative, revealing significant changes in the system dynamics. It is observed that lower fractional orders result in an extended bistability region. Also, chaos is only observed for larger magnetic strengths and fractional orders. Additionally, the application of the fractional-order model for image encryption is explored. The results demonstrate that the encryption based on the fractional model is efficient with high key sensitivity. It leads to an encrypted image with high entropy, neglectable correlation coefficient, and uniform distribution. Furthermore, the encryption system shows resistance to differential attacks, cropping attacks, and noise pollution. The Peak Signal-to-Noise Ratio (PSNR) calculations indicate that using a fractional derivative yields a higher PSNR compared to an integer derivative. Full article
(This article belongs to the Special Issue Chaotic Systems and Their Applications)
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Figure 1

Figure 1
<p>(<b>a</b>) Solutions of Equations (7a) (red color) and (7b) (blue color) with the intersection (0,0). The first equation is solved for <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>0.8</mn> <mo>,</mo> <mo> </mo> <mn>1.5</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mn>2</mn> </mrow> </semantics></math> and shown by different red tones. (<b>b</b>) The real part of the eigenvalues <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>λ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>λ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>. (<b>c</b>) The imaginary part of the eigenvalues <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>λ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>λ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>. (<b>d</b>) The argument of the eigenvalues <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>λ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>λ</mi> </mrow> <mrow> <mn>3</mn> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>(<b>a</b>) Bifurcation diagrams of the system as a function of magnetic coupling strength <math display="inline"><semantics> <mrow> <mi>k</mi> </mrow> </semantics></math> for different derivative orders. (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>1</mn> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.96</mn> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.94</mn> </mrow> </semantics></math>. The orange and blue colors correspond to two initial conditions, <math display="inline"><semantics> <mrow> <mo>(</mo> <mn>0.1</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>)</mo> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mo>(</mo> <mo>−</mo> <mn>0.1</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>)</mo> </mrow> </semantics></math>.</p>
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<p>Bifurcation diagram of the model as a function of <math display="inline"><semantics> <mrow> <mi>q</mi> </mrow> </semantics></math> for <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>1.2</mn> <mo>,</mo> <mn>1.4</mn> <mo>,</mo> <mn>1.6</mn> <mo>,</mo> <mn>1.8</mn> <mo>,</mo> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mn>2</mn> </mrow> </semantics></math>.</p>
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<p>The attractors of the model for <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>2.1</mn> </mrow> </semantics></math> and two initial conditions <math display="inline"><semantics> <mrow> <mo>(</mo> <mo>±</mo> <mn>0.1</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>)</mo> </mrow> </semantics></math>. (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>1</mn> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.96</mn> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.94</mn> </mrow> </semantics></math>.</p>
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<p>Time series corresponding to the attractors shown in <a href="#mathematics-11-04470-f004" class="html-fig">Figure 4</a> where <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>2.1</mn> </mrow> </semantics></math> and (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>1</mn> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.96</mn> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.94</mn> </mrow> </semantics></math>.</p>
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<p>Basin of attraction of two chaotic attractors for (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>1</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>1.5</mn> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>1.8</mn> </mrow> </semantics></math>, (<b>c</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.96</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>2.1</mn> </mrow> </semantics></math>, (<b>d</b>) <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.94</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>2.5</mn> </mrow> </semantics></math>.</p>
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<p>Flowchart of the encryption algorithm.</p>
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<p>Result of encryption method using the fractional-order system with <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>2</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math> and the initial condition <math display="inline"><semantics> <mrow> <mo>(</mo> <mn>0.1</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>)</mo> </mrow> </semantics></math>. (<b>a</b>,<b>d</b>) original images, (<b>b</b>,<b>e</b>) the encrypted images, (<b>c</b>,<b>f</b>) the decrypted images.</p>
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<p>Result of decryption with the wrong key. The encryption keys are <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>2</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>q</mi> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <mo>(</mo> <msub> <mrow> <mi>x</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>y</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>z</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> <mo>)</mo> <mo>=</mo> <mo>(</mo> <mn>0.1</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>)</mo> </mrow> </semantics></math>. (<b>a</b>,<b>d</b>) decrypted images with the correct key, (<b>b</b>,<b>e</b>) the decrypted images with <math display="inline"><semantics> <mrow> <mo>(</mo> <msub> <mrow> <mi>x</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>y</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> <mo>,</mo> <msub> <mrow> <mi>z</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> <mo>)</mo> <mo>=</mo> <mo>(</mo> <mn>0.100001</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>,</mo> <mo> </mo> <mn>0</mn> <mo>)</mo> </mrow> </semantics></math>, (<b>c</b>,<b>f</b>) the decrypted images with <math display="inline"><semantics> <mrow> <mi>k</mi> <mo>=</mo> <mn>1.99</mn> </mrow> </semantics></math>.</p>
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<p>The histogram of the colors of the original and encrypted images. (<b>a</b>) original onion image, (<b>b</b>) encrypted onion image, (<b>c</b>) original cameraman image, (<b>d</b>) encrypted cameraman image.</p>
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<p>The correlation of the color depth of two adjacent pixels. (<b>a</b>) original onion image, (<b>b</b>) encrypted onion image, (<b>c</b>) original cameraman image, (<b>d</b>) encrypted cameraman image.</p>
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<p>The result of the decryption of cropped images. (<b>a</b>) 1/64 of the image is cropped, (<b>b</b>) 1/16 of the image is cropped, (<b>c</b>) 1/4 of the image is cropped.</p>
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<p>The decrypted images from the noisy encrypted images with different intensities. (<b>a</b>,<b>d</b>) noise intensity is 0.05, (<b>b</b>,<b>e</b>) noise intensity is 0.1, (<b>c</b>,<b>f</b>) noise intensity is 0.2.</p>
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<p>Peak Signal-to-Noise Ratio of the decrypted image to the original image for different derivative orders. For each <span class="html-italic">q</span>, a range of <span class="html-italic">k</span> with monostable chaotic dynamics is adopted.</p>
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32 pages, 2601 KiB  
Article
Chemical and Biological Profiling of Fish and Seaweed Residues to Be Applied for Plant Fertilization
by Marios Maroulis, Sevasti Matsia, Georgios Lazopoulos, Oana Cristina Pârvulescu, Violeta Alexandra Ion, Oana-Crina Bujor, Joshua Cabell, Anne-Kristin Løes and Athanasios Salifoglou
Agronomy 2023, 13(9), 2258; https://doi.org/10.3390/agronomy13092258 - 28 Aug 2023
Cited by 2 | Viewed by 2378
Abstract
Brown algae and fish waste contain high-value compounds with potentially beneficial effects on plant growth. Several commercial fertilizer products are currently available, but the characteristics of the materials are usually not well-described. Fish and seaweed residues originating from the Norwegian coast are available, [...] Read more.
Brown algae and fish waste contain high-value compounds with potentially beneficial effects on plant growth. Several commercial fertilizer products are currently available, but the characteristics of the materials are usually not well-described. Fish and seaweed residues originating from the Norwegian coast are available, after industrial processing, which may be combined into complete fertilizers exerting additional effects on crop plants (biostimulants). In this study, raw samples of fish and seaweed residues were investigated using ecofriendly technologies (drying, leaching), targeting search and isolation of potential biostimulants, followed by physicochemical characterization (elemental analysis, UV–visible, FT-IR, ICP-MS, ICP-OES, electrical conductivity, pH, etc.). Organic solvent extractions were employed to determine the available mineral content, micro- and macro-nutrients, antioxidant compounds, and amino acid content by chemical hydrolysis. The in vitro biotoxicity profile (cell viability, morphology, migration) of the generated extracts was also perused, employing Gram-positive (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli) along with sensitive neuronal eukaryotic cell lines N2a58 and SH-SY5Y, to assess their time- and concentration-dependent efficacy as antimicrobials and agents counteracting oxidative stress. The analytical composition of all raw materials showed that they contain important nutrients (K, P, Ca, N) as well as organic compounds and amino acids (Gly, Asp, Glu, Leu, Phe) capable of acting as plant biostimulants. Concurrently, the inherently high conductivity values and salt content necessitated leaching processes, which result in Na+ and K+ decreasing by more than ~60% and justifying further their use in soil treatment formulations. The aforementioned results and assertions, combined with physical measurements (pH, electrical conductivity, etc.) on naturally occurring and dried samples as well as green solvent extracts, formulated a physicochemical profile reflecting well-defined inorganic–organic species that might function as biostimulants. The collective physicochemical and biological properties support the notion that appropriate mixtures of marine organism residues may be efficient fertilizers for crop plants and concurrently possess biostimulant characteristics. Full article
(This article belongs to the Section Agroecology Innovation: Achieving System Resilience)
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<p>FC-FID chromatograms for <b>HNSW</b>, <b>LNSW</b>, and <b>GFB</b> samples. Each chromatogram is of a different color, corresponding to each one of the three samples employed (HNSW, red; LNSW, blue; GFB, green).</p>
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<p>Comparative GC–MS spectra for <b>HNSW</b> and <b>LNSW</b> samples in ethyl acetate (<b>EA</b>) and hexane (<b>H</b>) solvents.</p>
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<p>Growth rate of (<b>A</b>) <span class="html-italic">E. coli</span>, and (<b>B</b>) <span class="html-italic">S. aureus</span> in in vitro liquid cell cultures exposed to ethyl acetate extracts. The experimental graphs (a) are depicted in different colors, (b) include all three types of samples employed (HNSW, LNSW, GFB), (c) reflect all DMSO concentrations used (1, 5, 10%), and (d) involve the appropriate controls (LB broth and antibiotics penicillin-streptomycin), as shown on the side of the Figure.</p>
Full article ">Figure 3 Cont.
<p>Growth rate of (<b>A</b>) <span class="html-italic">E. coli</span>, and (<b>B</b>) <span class="html-italic">S. aureus</span> in in vitro liquid cell cultures exposed to ethyl acetate extracts. The experimental graphs (a) are depicted in different colors, (b) include all three types of samples employed (HNSW, LNSW, GFB), (c) reflect all DMSO concentrations used (1, 5, 10%), and (d) involve the appropriate controls (LB broth and antibiotics penicillin-streptomycin), as shown on the side of the Figure.</p>
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<p>In vitro cell viability in the presence of <b>GFB-E-EA</b> for 24, 48, and 72 h in (<b>A</b>) N2a58, and (<b>B</b>) SH-SY5Y neuronal cell cultures in a concentration-dependent fashion (with details provided in the text). Significance levels were assessed as follows: * <span class="html-italic">p</span> &lt; 0.05 (significant), ** <span class="html-italic">p</span> &lt; 0.01 (highly significant), and **** <span class="html-italic">p</span> ≤ 0.0001 (extremely significant) or non-significant (<span class="html-italic">p</span> &gt; 0.05).</p>
Full article ">Figure 4 Cont.
<p>In vitro cell viability in the presence of <b>GFB-E-EA</b> for 24, 48, and 72 h in (<b>A</b>) N2a58, and (<b>B</b>) SH-SY5Y neuronal cell cultures in a concentration-dependent fashion (with details provided in the text). Significance levels were assessed as follows: * <span class="html-italic">p</span> &lt; 0.05 (significant), ** <span class="html-italic">p</span> &lt; 0.01 (highly significant), and **** <span class="html-italic">p</span> ≤ 0.0001 (extremely significant) or non-significant (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Cell morphology studies of <b>HNSW-E-EA</b>, <b>LNSW-E-EA</b>, and <b>GFB-E-EA</b> in N2a58 neuronal cell cultures for 0, 24, 48, and 72 h, at the highest concentration of extracts investigated (<b>HNSW-E-EA</b>, 28.0 × 10<sup>2</sup> ng<sub>extract</sub>/g of dry HNSW/mL DMSO; <b>LNSW-E-EA</b>, 24.6 × 10<sup>2</sup> ng<sub>extract</sub>/g of dry LNSW/mL DMSO, and <b>GFB-E-EA</b>, 64.8 × 10<sup>2</sup> ng<sub>extract</sub>/g of dry GFB/mL DMSO).</p>
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<p>Migration studies of <b>HNSW-E-EA</b>, <b>LNSW-E-EA</b>, and <b>GFB-E-EA</b> in SH-SY5Y neuronal cell cultures for 0, 24, 48, and 72 h, at the highest concentration of extracts investigated (<b>HNSW-E-EA</b>, 28.0 × 10<sup>2</sup> ng<sub>extract</sub>/g dry HNSW/mL DMSO; <b>LNSW-E-EA</b>, 24.6 × 10<sup>2</sup> ng<sub>extract</sub>/g dry LNSW/mL DMSO, and <b>GFB-E-EA</b>, 64.8 × 10<sup>2</sup> ng<sub>extract</sub>/g dry GFB/mL DMSO). Close ups of the provided experiments, provide tangible proof of the progress of cell migration during the investigation.</p>
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29 pages, 12305 KiB  
Article
APO-ELM Model for Improving Azimuth Correction of Shipborne HFSWR
by Yaning Wang, Haibo Yu, Ling Zhang and Gangsheng Li
Remote Sens. 2023, 15(15), 3818; https://doi.org/10.3390/rs15153818 - 31 Jul 2023
Cited by 1 | Viewed by 1254
Abstract
Shipborne high-frequency surface wave radar (HFSWR) has a wide range of applications and plays an important role in moving target detection and tracking. However, the complexity of the sea detection environment causes the target signals received by shipborne HFSWR to be seriously disturbed [...] Read more.
Shipborne high-frequency surface wave radar (HFSWR) has a wide range of applications and plays an important role in moving target detection and tracking. However, the complexity of the sea detection environment causes the target signals received by shipborne HFSWR to be seriously disturbed by sea clutter. Sea clutter increases the difficulty of azimuth estimation, resulting in a challenging problem for shipborne HFSWR. To solve this problem, a novel azimuth correction method based on adaptive boosting error feedback dynamic weighted particle swarm optimization extreme learning machine (APO-ELM) is proposed to improve the azimuth estimation accuracy of shipborne HFSWR. First, the sea clutter is modeled and simulated. Then, we study its characteristics and analyze the influence of its characteristics on the first-order clutter spectrum and target detection accuracy, respectively. In addition, the proposed improved particle swarm optimization (PSO) and adaptive neuron clipping algorithm are used to optimize the input parameters of the ELM network. Then, the network performs error feedback based on the optimized parameter performance and updates the feature matrix, which can give a minimum clutter-error estimation. After that, it iteratively trains multiple weak learners using the adaptive boosting (AdaBoost) algorithm to form a strong learner and make strong predictions. Finally, after error compensation, the best azimuth estimation results are obtained. The sample sets used for the APO-ELM network are obtained from field shipborne HFSWR data. The network training and testing features include the wind direction, sea current, wind speed, platform speed, and signal-to-clutter ratio (SCR). The experimental results show that this method has a lower root-mean-square error than the back-propagation neural network and support vector regression (SVR) azimuth correction methods, which verifies the effectiveness of the proposed method. Full article
(This article belongs to the Special Issue Feature Paper Special Issue on Ocean Remote Sensing - Part 2)
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<p>First-order sea surface echo space-frequency distribution characteristics of (<b>a</b>) shore-based HFSWR and (<b>b</b>) shipborne HFSWR.</p>
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<p>Schematic diagram of sea echo.</p>
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<p>Simulation results: (<b>a</b>) Sea clutter RD spectrum, with target information added; (<b>b</b>) 1D spectrogram of the distance cell where the target is located; (<b>c</b>) Result obtained by DBF of the target.</p>
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<p>(<b>a</b>) Effect of wind speed on target azimuth error; (<b>b</b>) Effect of wind speed on the Doppler spectrum of the distance cell where the target (−25°) is located.</p>
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<p>RD spectrum. (<b>a</b>) Parameters: wind speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind direction 45°, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB. (<b>b</b>) Parameters: wind speed 10 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind direction 45°, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB.</p>
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<p>Wind direction diagram.</p>
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<p>(<b>a</b>) Effect of wind direction on target azimuth error; (<b>b</b>) Effect of wind speed on the Doppler spectrum of the distance cell where the target (−25°) is located.</p>
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<p>RD spectrum. (<b>a</b>) Parameters: wind direction 45°, wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.1 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB; (<b>b</b>) Parameters: wind direction 315°, wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.1 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB; (<b>c</b>) Parameters: wind direction 180°,wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.1 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB.</p>
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<p>(<b>a</b>) Effect of sea current on target azimuth error; (<b>b</b>) Effect of currents on the Doppler spectrum of the distance cell where the target (−25°) is located.</p>
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<p>RD spectrum. (<b>a</b>) Parameters: current speed 0.3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind direction 45°, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB; (<b>b</b>) Parameters: current speed 1.2 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind direction 45°, platform speed 3 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, and SCR 3 dB.</p>
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<p>(<b>a</b>) Effect of platform speed on the echo spectrum; (<b>b</b>) First-order echo spectrum of excessive ship speed; (<b>c</b>) Effect of platform forward motion on target azimuth error; (<b>d</b>) Effect of platform forward motion on the Doppler spectrum of the distance cell where the target (−25°) is located.</p>
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<p>RD spectrum. (<b>a</b>) Parameters: platform speed 1 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.2 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind direction 45°, and SCR 3 dB; (<b>b</b>) Parameters: platform speed 8 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind speed 5 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, current speed 0.2 <math display="inline"><semantics> <mrow> <mrow> <mi mathvariant="normal">m</mi> <mo>/</mo> <mi mathvariant="normal">s</mi> </mrow> </mrow> </semantics></math>, wind direction 45°, and SCR 3 dB.</p>
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<p>Image of the probability density function of the beta distribution.</p>
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<p>EDPO-ELM network model schematic.</p>
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<p>APO-ELM network framework schematic.</p>
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<p>(<b>a</b>) Processing flowchart of azimuth correction based on APO-ELM; (<b>b</b>) RD spectrum with targets detected by HFSWR (marked with black circles) and AIS (marked with black crosses).</p>
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<p>(<b>a</b>) Trend of RMSE based on the number of hidden layer neurons on the network model under the <math display="inline"><semantics> <mrow> <mrow> <mi>Sigmoid</mi> <mo>(</mo> </mrow> <mo>·</mo> <mo>)</mo> </mrow> </semantics></math> function; (<b>b</b>) Trend of network model accuracy based on the number of hidden layer neurons under the <math display="inline"><semantics> <mrow> <mrow> <mi>Sigmoid</mi> <mo>(</mo> </mrow> <mo>·</mo> <mo>)</mo> </mrow> </semantics></math> function.</p>
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<p>Relationship between the weight coefficient ratio and the number of neurons in the hidden layer.</p>
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<p>(<b>a</b>) Effect of the number of weak learners on the accuracy of the strong learner model; (<b>b</b>) Effect of the number of weak learners on the time consumption of the strong learner model.</p>
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<p>Target azimuth correction results.</p>
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<p>Azimuth correction results of BP, SVR, ELM, PSO-ELM, EDPO-ELM, and the proposed method. (<b>a</b>) Errors of different target azimuth correction algorithms; (<b>b</b>) Azimuth estimation results of different algorithms.</p>
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28 pages, 6036 KiB  
Article
An Accurate Classification of Rice Diseases Based on ICAI-V4
by Nanxin Zeng, Gufeng Gong, Guoxiong Zhou and Can Hu
Plants 2023, 12(11), 2225; https://doi.org/10.3390/plants12112225 - 5 Jun 2023
Cited by 19 | Viewed by 3343
Abstract
Rice is a crucial food crop, but it is frequently affected by diseases during its growth process. Some of the most common diseases include rice blast, flax leaf spot, and bacterial blight. These diseases are widespread, highly infectious, and cause significant damage, posing [...] Read more.
Rice is a crucial food crop, but it is frequently affected by diseases during its growth process. Some of the most common diseases include rice blast, flax leaf spot, and bacterial blight. These diseases are widespread, highly infectious, and cause significant damage, posing a major challenge to agricultural development. The main problems in rice disease classification are as follows: (1) The images of rice diseases that were collected contain noise and blurred edges, which can hinder the network’s ability to accurately extract features of the diseases. (2) The classification of disease images is a challenging task due to the high intra-class diversity and inter-class similarity of rice leaf diseases. This paper proposes the Candy algorithm, an image enhancement technique that utilizes improved Canny operator filtering (the gravitational edge detection algorithm) to emphasize the edge features of rice images and minimize the noise present in the images. Additionally, a new neural network (ICAI-V4) is designed based on the Inception-V4 backbone structure, with a coordinate attention mechanism added to enhance feature capture and overall model performance. The INCV backbone structure incorporates Inception-iv and Reduction-iv structures, with the addition of involution to enhance the network’s feature extraction capabilities from a channel perspective. This enables the network to better classify similar images of rice diseases. To address the issue of neuron death caused by the ReLU activation function and improve model robustness, Leaky ReLU is utilized. Our experiments, conducted using the 10-fold cross-validation method and 10,241 images, show that ICAI-V4 has an average classification accuracy of 95.57%. These results indicate the method’s strong performance and feasibility for rice disease classification in real-life scenarios. Full article
(This article belongs to the Collection Application of AI in Plants)
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<p>Process of acquisition, transmission, enhancement (flip, crop), and preprocessing of four rice disease images.</p>
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<p>Main flow chart of rice disease classification.</p>
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<p>Main process of rice leaf image processing with Candy algorithm.</p>
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<p>Picture utilizing the gravitational edge detection algorithm and Candy algorithm for processing rice leaf images.</p>
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<p>Block diagram of ICAI-V4 model. It includes INCV blocks and coordinate attention network structure.</p>
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<p>Schematic diagram of involution.</p>
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<p>Accuracy of 10-fold cross-validation training results.</p>
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<p>Classification confusion matrix of citrus diseases by different models (the models corresponding to the (<b>A</b>–<b>G</b>) confusion matrix are: AlexNet, ResNet50, Inceptionv4, ResNeXt, MobileNetv3, DenseNet121, and ICAI-V4).</p>
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16 pages, 696 KiB  
Article
Influence of Hyperparameters in Deep Learning Models for Coffee Rust Detection
by Adrian F. Chavarro, Diego Renza and Dora M. Ballesteros
Appl. Sci. 2023, 13(7), 4565; https://doi.org/10.3390/app13074565 - 4 Apr 2023
Cited by 5 | Viewed by 1976
Abstract
Most of the world’s crops can be attacked by various diseases or pests, affecting their quality and productivity. In recent years, transfer learning with deep learning (DL) models has been used to detect diseases in maize, tomato, rice, and other crops. In the [...] Read more.
Most of the world’s crops can be attacked by various diseases or pests, affecting their quality and productivity. In recent years, transfer learning with deep learning (DL) models has been used to detect diseases in maize, tomato, rice, and other crops. In the specific case of coffee, some recent works have used fixed hyperparameters to fine-tune the pre-trained models with the new dataset and/or applied data augmentation, such as image patching, to improve classifier performance. However, a detailed evaluation of the impact of architecture (e.g., backbone) and training (e.g., optimizer and learning rate) hyperparameters on the performance of coffee rust classification models has not been performed. Therefore, this paper presents a comprehensive study of the impact of five types of hyperparameters on the performance of coffee rust classification models. Specifically, eight pre-trained models are compared, each with four different amounts of transferred layers and three different numbers of neurons in the fully-connected (FC) layer, and the models are fine-tuned with three types of optimizers, each with three learning rate values. Comparing more than 800 models in terms of F1-score and accuracy, it is identified that the type of backbone is the hyperparameter with the greatest impact (with differences between models of up to 70%), followed by the optimizer (with differences of up to 20%). At the end of the study, specific recommendations are made on the values of the most suitable hyperparameters for the identification of this type of disease in coffee crops. Full article
(This article belongs to the Special Issue AI-Based Image Processing)
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<p>Schematic representation of transfer learning. Typically, dataset B is much smaller than dataset A. The classifier block contains new fully-connected (FC) layers and the output of the model.</p>
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<p>Proposed methodology for quantitative evaluation of coffee rust detection models using transfer learning.</p>
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<p>Different levels of coffee rust severity. The higher the level, the more the coffee leaf is affected by coffee rust. Level 1 implies that between 1% to 5% of the leaf has rust, level 2 means that between 6% to 20% of the leaf is affected, level 3 has an affectation between 21% to 50% of the leaf, while level 4 implies that more than 50% of the leaf has rust.</p>
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<p>Summary of evaluation results by pre-trained model used as a backbone, in terms of F1-score. Points marked with + represent outliers beyond the first and third quartiles.</p>
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<p>Summary of evaluation results by optimizer, in terms of F1-score.</p>
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<p>Evaluation results for VGG19 model by learning rate and Optimizer, in terms of F1-score.</p>
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<p>Summary of evaluation results by learning rate and model type, in terms of F1-score.</p>
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<p>Summary of evaluation results by the number of neurons in the last FC layer (except the output layer), in terms of F1-score.</p>
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<p>Summary of evaluation results by the last layer transfered, in terms of F1-score.</p>
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<p>Confusion matrices of the models obtained from DenseNet201, Xception, MobileNetV2, Inception, VGG19 and InceptionResNetV2, by transfer learning. Multi-class classification with 0: Healthy, 1: Other, and 2: Rust. The darker the grid, the greater the number of cases located in that condition.</p>
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17 pages, 3285 KiB  
Article
Hyperspectral Non-Imaging Measurements and Perceptron Neural Network for Pre-Harvesting Assessment of Damage Degree Caused by Septoria/Stagonospora Blotch Diseases of Wheat
by Sofia V. Zhelezova, Elena V. Pakholkova, Vladislav E. Veller, Mikhail A. Voronov, Eugenia V. Stepanova, Alena D. Zhelezova, Anton V. Sonyushkin, Timur S. Zhuk and Alexey P. Glinushkin
Agronomy 2023, 13(4), 1045; https://doi.org/10.3390/agronomy13041045 - 1 Apr 2023
Cited by 5 | Viewed by 2363
Abstract
The detection and identification of plant diseases is a fundamental task for sustainable crop production. Septoria tritici and Stagonospora nodorum blotch (STB and SNB) are two of the most common diseases of cereal crops that cause significant economic damage. Both pathogens are difficult [...] Read more.
The detection and identification of plant diseases is a fundamental task for sustainable crop production. Septoria tritici and Stagonospora nodorum blotch (STB and SNB) are two of the most common diseases of cereal crops that cause significant economic damage. Both pathogens are difficult to identify at early stages of infection. Determining the degree of the disease at a late infection stage is useful for assessing cereal crops before harvesting, as it allows the assessment of potential yield losses. Hyperspectral sensing could allow for automatic recognition of Septoria harmfulness on wheat in field conditions. In this research, we aimed to collect information on the hyperspectral data on wheat plants with different lesion degrees of STB&SNB and to create and train a neural network for the detection of lesions on leaves and ears caused by STB&SNB infection at the late stage of disease development. Spring wheat was artificially infected twice with Septoria pathogens in the stem elongation stage and in the heading stage. Hyperspectral reflections and brightness measurements were collected in the field on wheat leaves and ears on the 37th day after STB and the 30th day after SNB pathogen inoculation using an Ocean Insight “Flame” VIS-NIR hyperspectrometer. Obtained non-imaging data were pre-treated, and the perceptron model neural network (PNN) was created and trained based on a pairwise comparison of datasets for healthy and diseased plants. Both statistical and neural network approaches showed the high quality of the differentiation between healthy and damaged wheat plants by the hyperspectral signature. A comparison of the results of visual recognition and automatic STB&SNB estimation showed that the neural network was equally effective in the quality of the disease definition. The PNN, based on a neuron model of hyperspectral signature with a spectral step of 6 nm and 2000–4000 value datasets, showed a high quality of detection of the STB&SNB severity. There were 0.99 accuracy, 0.94 precision, 0.89 recall and 0.91 F-score metrics of the PNN model after 10,000 learning epochs. The estimation accuracy of diseased/healthy leaves ranged from 88.1 to 97.7% for different datasets. The accuracy of detection of a light and medium degree of disease was lower (38–66%). This method of non-imaging hyperspectral signature classification could be useful for the identification of the STB and SNB lesion degree identification in field conditions for pre-harvesting crop estimation. Full article
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<p>The degrees of septoriosis disease severity on spring wheat leaves and ears: (<b>a</b>) healthy leaf; (<b>b</b>) medium lesion on leaf; (<b>c</b>) severe lesion on leaf; (<b>d</b>) healthy ear; (<b>e</b>) medium lesion on ear; (<b>f</b>) severe lesion on ear.</p>
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<p>The perceptron neural network architecture. Inputs p1, p2… pr are the hyperspectral signatures from one dataset.</p>
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<p>Hyperspectral curves of one dataset after preprocessing of raw data (each chart includes 2000 curves): (<b>a</b>) curves of healthy leaf, (<b>b</b>) curves of leaf in medium stage of Septoria disease.</p>
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<p>Two examples of curve dataset clusterization: (<b>a</b>) cluster of typical curves of healthy leaves; (<b>b</b>) cluster of invalid curves of healthy leaves; (<b>c</b>) cluster of typical curves of leaves with severe lesions caused by Septoria; (<b>d</b>) cluster of non-typical (invalid) curves of leaves with severe lesions caused by Septoria.</p>
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<p>Datasets of means and quantiles of variety of hyperspectral curves of leaves: (<b>a</b>,<b>c</b>,<b>e</b>)—means of healthy, medium-damaged and severely damaged leaves, respectively; (<b>b</b>,<b>d</b>,<b>f</b>) quantile distribution of the same datasets.</p>
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<p>Dataset means and quantiles of variety of hyperspectral curves of ears: (<b>a</b>,<b>c</b>,<b>e</b>)—means of healthy, medium-damaged and severely damaged ears, respectively; (<b>b</b>,<b>d</b>,<b>f</b>) quantile distribution of the same datasets.</p>
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<p>Hyperspectral curves of reflectance of leaves (<b>a</b>,<b>c</b>,<b>e</b>) and ears (<b>b</b>,<b>d</b>,<b>f</b>)—means of healthy, medium-damaged and severely damaged leaves and ears, respectively, and values of the angle (%) between the branches of the graph.</p>
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<p>Regression relationship between the degree of septoriosis lesion and yield loss: (<b>a</b>) STB lesion of flag-leaf; (<b>b</b>) SNB lesion of ears. Every circle is an individual measurement from the plot with studied wheat cultivar.</p>
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15 pages, 445 KiB  
Article
Deep Learning-Based Method for Classification of Sugarcane Varieties
by Priscila Marques Kai, Bruna Mendes de Oliveira and Ronaldo Martins da Costa
Agronomy 2022, 12(11), 2722; https://doi.org/10.3390/agronomy12112722 - 2 Nov 2022
Cited by 12 | Viewed by 3047
Abstract
The classification of sugarcane varieties using products derived from remote sensing allows for the monitoring of plants with different profiles without necessarily having physical contact with the study objects. However, differentiating between varieties can be challenging due to the similarity of the spectral [...] Read more.
The classification of sugarcane varieties using products derived from remote sensing allows for the monitoring of plants with different profiles without necessarily having physical contact with the study objects. However, differentiating between varieties can be challenging due to the similarity of the spectral characteristics of each crop. Thus, this study aimed to classify four sugarcane varieties through deep neural networks, subsequently comparing the results with traditional machine learning techniques. In order to provide more data as input for the classification models, along with the multi-band values of the pixels and vegetation indices, other information can be obtained from the sensor bands through RGB combinations by reconciling different bands so as to yield the characteristics of crop varieties. The methodology created to discriminate sugarcane varieties consisted of a dense neural network, with the number of hidden layers determined by the greedy layer-wise method and multiples of four neurons in each layer; additionally, a 5-fold evaluation in the training data was composed of Sentinel-2 band data, vegetation indices, and RGB combinations. Comparing the results acquired from each model with the hyperparameters selected by Bayesian optimisation, except for the neural network with manually defined parameters, it was possible to observe a greater precision of 99.55% in the SVM model, followed by the neural network developed by the study, random forests, and kNN. However, the final neural network model prediction resulted in the 99.48% accuracy of a six-hidden-layers network, demonstrating the potential of using neural networks in classification. Among the characteristics that contributed the most to the classification, the chlorophyll-sensitive bands, especially B6, B7, B11, and some RGB combinations, had the most impact on the correct classification of samples by the neural network model. Thus, the regions encompassing the near-infrared and shortwave infrared regions proved to be suitable for the discrimination of sugarcane varieties. Full article
(This article belongs to the Special Issue Applications of Deep Learning Techniques in Agronomy)
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<p>Sugarcane harvest cycle of varieties RB867515, RB92579, RB966928, and RB988082.</p>
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<p>Database for the experiments. Each sample is composed of values from each Sentinel-2 band (except for band 10), vegetation indices, and combinations of the Sentinel-2 bands.</p>
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<p>Flowchart for classifying sugarcane varieties.</p>
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<p>Evaluation of the dense neural network model according to the number of layers added.</p>
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<p>Evaluation of the dense neural network model according to the number of hidden layers added for bands, vegetation indices, and RGB combinations.</p>
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<p>The five most significant features as input in the neural network model for the correct classification of sugarcane varieties. Among the characteristics, the bands B6 (band 6—Vegetation Red Edge), B1 (band 1—Coastal Aerosol), B7 (band 7—Vegetation Red-Edge), B11 (band 11—SWIR), and combination C1 (band 8, band 6, and band 4).</p>
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<p>The five most significant features as input in the SVM model for the correct classification of sugarcane varieties. Respectively, the Sentinel-2 bands B6 (band 6—Vegetation Red-Edge), B7 (band 7—Vegetation Red-Edge), combination C1 (band 8, band 6, and band 4), B11 (band 11—SWIR), and B2 (band 2—Blue).</p>
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13 pages, 4986 KiB  
Article
The Neurotoxic Effect of Ochratoxin-A on the Hippocampal Neurogenic Niche of Adult Mouse Brain
by Eva Mateo, Rik Paulus Bernardus Tonino, Antolin Canto, Antonio Monroy Noyola, Maria Miranda, Jose Miguel Soria and María Angeles Garcia Esparza
Toxins 2022, 14(9), 624; https://doi.org/10.3390/toxins14090624 - 6 Sep 2022
Cited by 6 | Viewed by 2664
Abstract
Ochratoxin A (OTA) is a common secondary metabolite of Aspergillus ochraceus, A. carbonarius, and Penicillium verrucosum. This mycotoxin is largely present as a contaminant in several cereal crops and human foodstuffs, including grapes, corn, nuts, and figs, among others. Preclinical [...] Read more.
Ochratoxin A (OTA) is a common secondary metabolite of Aspergillus ochraceus, A. carbonarius, and Penicillium verrucosum. This mycotoxin is largely present as a contaminant in several cereal crops and human foodstuffs, including grapes, corn, nuts, and figs, among others. Preclinical studies have reported the involvement of OTA in metabolic, physiologic, and immunologic disturbances as well as in carcinogenesis. More recently, it has also been suggested that OTA may impair hippocampal neurogenesis in vivo and that this might be associated with learning and memory deficits. Furthermore, aside from its widely proven toxicity in tissues other than the brain, there is reason to believe that OTA contributes to neurodegenerative disorders. Thus, in this present in vivo study, we investigated this possibility by intraperitoneally (i.p.) administering 3.5 mg OTA/kg body weight to adult male mice to assess whether chronic exposure to this mycotoxin negatively affects cell viability in the dentate gyrus of the hippocampus. Immunohistochemistry assays showed that doses of 3.5 mg/kg caused a significant and dose-dependent reduction in repetitive cell division and branching (from 12% to 62%). Moreover, the number of countable astrocytes (p < 0.001), young neurons (p < 0.001), and mature neurons (p < 0.001) negatively correlated with the number of i.p. OTA injections administered (one, two, three, or six repeated doses). Our results show that OTA induced adverse effects in the hippocampus cells of adult mice brain tissue when administered in cumulative doses. Full article
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<p>The chemical structure of ochratoxin A.</p>
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<p>Photomicrographs of GFAP-labeled cells in the control, OTA1, OTA2, OTA3, and OTA6 groups (which received one to six injections of ochratoxin A, respectively), taken at 20× magnification. Compared to the control, the number of GFAP-positive cells decreased as the number of ochratoxin A treatments increased. (Control n = 4, OTA1 n = 4, OTA2 n = 4, OTA3 n = 4, OTA6 n = 5). ** = <span class="html-italic">p</span> &lt; 0.01, and *** = <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Individual GFAP-labeled cells in the control group and after two (O2) or six (O6) doses of ochratoxin A. Note how the morphology of these cells changed as the number of doses increased, with the cellular body appearing to decrease in volume and the cytoplasmic processes retracting. These photomicrographs were obtained at a 40× magnification.</p>
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<p>Photomicrographs of GFAP-labeled cells in the control, OTA2, OTA3, and OTA6 groups (which received two, three, or six ochratoxin A injections, respectively) at a 20× magnification Compared to the control: *** = <span class="html-italic">p</span> &lt; 0.001. An example of the branch quantification and the branches per cell and branch lengths for each photo are also shown. (Control n = 4, OTA2 n = 4, OTA3 n = 4, OTA6 n = 5).</p>
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<p>Photomicrographs of DCX-labeled cells in the dentate gyrus of the control, OTA1, OTA2, OTA3, and OTA6 groups (which received one to six injections with ochratoxin A, respectively) at a magnification of 20×. Compared to the control, the number of DCX-positive cells decreased as the number of ochratoxin A treatments increased: *** = <span class="html-italic">p</span> &lt; 0.001. Games–Howell statistical analysis. (Control n = 4, OTA1 n = 4, OTA2 n = 4, OTA3 n = 4, OTA6 n = 5).</p>
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<p>Photomicrographs of individual DCX-labeled young neurons demonstrating small morphological changes as the doses of ochratoxin A increased. The sizes of the cells appear to have decreased compared to the control group, although these changes do not appear to be as prominent as with the GFAP-labeled cells.</p>
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<p>Photomicrographs of MAP2-labeled cells in the dentate gyrus of the control, O1, O2, O3, and O6 groups taken at a 20× magnification. Compared to the control, the number of MAP2-positive cells decreased as the number of ochratoxin A treatments increased. *** = <span class="html-italic">p</span> &lt; 0.001). Statistical analysis was one-way ANOVA with a post-hoc LSD test. (Control n = 4, OTA1 n = 4, OTA2 n = 4, OTA3 n = 4, OTA6 n = 5).</p>
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<p>Photomicrographs of individual MAP2-labeled mature neurons and DAPI-labeled nuclei demonstrating their changing morphology as the number of doses of ochratoxin A increased. Whereas many dendrites and cells were present in the control, no comparable structures were present in the O6 group (6 doses of ochratoxin A). Very few dendrites could be found, and the cell body fluorescence was strongly decreased in the O6 group. The images were taken at a 40× magnification and digitally magnified to 400×. The arrow indicates a Map2/DAPI co-labeled cell.</p>
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22 pages, 3519 KiB  
Article
Enhancing Smallholder Wheat Yield Prediction through Sensor Fusion and Phenology with Machine Learning and Deep Learning Methods
by Andualem Aklilu Tesfaye, Berhan Gessesse Awoke, Tesfaye Shiferaw Sida and Daniel E. Osgood
Agriculture 2022, 12(9), 1352; https://doi.org/10.3390/agriculture12091352 - 1 Sep 2022
Cited by 9 | Viewed by 2836
Abstract
Field-scale prediction methods that use remote sensing are significant in many global projects; however, the existing methods have several limitations. In particular, the characteristics of smallholder systems pose a unique challenge in the development of reliable prediction methods. Therefore, in this study, a [...] Read more.
Field-scale prediction methods that use remote sensing are significant in many global projects; however, the existing methods have several limitations. In particular, the characteristics of smallholder systems pose a unique challenge in the development of reliable prediction methods. Therefore, in this study, a fast and reproducible new approach to wheat prediction is developed by combining predictors derived from optical (Sentinel-2) and radar (Sentinel-1) sensors using a diverse set of machine learning and deep learning methods under a small dataset domain. This study takes place in the wheat belt region of Ethiopia and evaluates forty-two predictors that represent the major vegetation index categories of green, water, chlorophyll, dry biomass, and VH polarization SAR indices. The study also applies field-collected agronomic data from 165 farm fields for training and validation. According to results, compared to other methods, a combined automated machine learning (AutoML) approach with a generalized linear model (GLM) showed higher performance. AutoML, which reduces training time, delivered ten influential parameters. For the combined approach, the mean RMSE of wheat yield was from 0.84 to 0.98 ton/ha using ten predictors from the test dataset, achieving a 99% confidence interval. It also showed a correlation coefficient as high as 0.69 between the estimated yield and measured yield, and it was less sensitive to the small datasets used for model training and validation. A deep neural network with three hidden layers using the ten influential parameters was the second model. For this model, the mean RMSE of wheat yield was between 1.31 and 1.36 ton/ha on the test dataset, achieving a 99% confidence interval. This model used 55 neurons with respective values of 0.1, 0.5, and 1 × 10−4 for the hidden dropout ratio, input dropout ratio, and l2 regularization. The approaches implemented in this study are fast and reproducible and beneficial to predict yield at scale. These approaches could be adapted to predict grain yields of other cereal crops grown under smallholder systems in similar global production systems. Full article
(This article belongs to the Section Digital Agriculture)
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<p>Location of the study area (<b>a</b>), study districts (<b>b</b>) and farm distribution (points) (<b>b</b>) as well as some farm boundaries (polygons), (<b>c</b>) and histogram of study farm areas.</p>
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<p>Flow diagram showing the input dataset, derivation of predictors, and the three algorithms used.</p>
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<p>Scatter plots of SAR indices of single growth stage (<span class="html-italic">x</span>−axis) vs. grain yield (<span class="html-italic">y</span>−axis) for tillering and grain-filling stage.</p>
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<p>Scatter plots of SAR indices of single growth stage (<span class="html-italic">x</span>−axis) and grain yield (<span class="html-italic">y</span>−axis) for post-grain-filling stage.</p>
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<p>Scatter plots showing the non-linear models for three indices using combined-date VH polarization (db). Sub plots (<b>a</b>–<b>c</b>) represent non-linear model results of the SND, SSD, and SSR indices, respectively.</p>
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<p>Scatter plots showing the performance of GLM on the test dataset for six randomly selected seeds. The red lines represent a 1:1 line between estimated and measured yields. (<b>A</b>–<b>F</b>) refer to six plots prepared using six randomly generated numbers (seeds).</p>
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<p>Histogram of measured yield with mean and median values.</p>
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<p>Table showing the number of neurons against error metrics (RMSE, MAE, and RMSLE) for one hidden layer in the validation group. The three metrics are average values.</p>
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<p>Table showing the number of neurons for the range of 0–1000 against error metrics (RMSE, MAE, and RMSLE) for one hidden layer in the validation group. The three metrics are average values.</p>
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<p>Table showing number of neurons against error metrics (RMSE, MAE, and RMSLE) for three numbers of hidden layers in the validation group. The three metrics are average values.</p>
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<p>Scatter plots showing the performance of DNN with three hidden layers on the test dataset for six randomly selected seeds. (<b>A</b>–<b>F</b>) refer to six plots prepared using six randomly generated numbers (seeds).</p>
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<p>A plot showing the top ten most influential variables using the GLM model.</p>
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<p>A plot showing the top ten most influential variables using the GBM model.</p>
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20 pages, 4657 KiB  
Article
The Efficacy of Camelina sativa Defatted Seed Meal against Colitis-Induced Persistent Visceral Hypersensitivity: The Relevance of PPAR α Receptor Activation in Pain Relief
by Elena Lucarini, Laura Micheli, Eleonora Pagnotta, Alessandra Toti, Valentina Ferrara, Clara Ciampi, Francesco Margiotta, Alma Martelli, Lara Testai, Vincenzo Calderone, Roberto Matteo, Serafino Suriano, Antonio Troccoli, Nicola Pecchioni, Clementina Manera, Lorenzo Di Cesare Mannelli and Carla Ghelardini
Nutrients 2022, 14(15), 3137; https://doi.org/10.3390/nu14153137 - 29 Jul 2022
Cited by 7 | Viewed by 2591
Abstract
Brassicaceae are natural sources of bioactive compounds able to promote gut health. Belonging to this plant family, Camelina sativa is an ancient oil crop rich in glucosinolates, polyunsaturated fatty acids, and antioxidants that is attracting renewed attention for its nutraceutical potential. This work [...] Read more.
Brassicaceae are natural sources of bioactive compounds able to promote gut health. Belonging to this plant family, Camelina sativa is an ancient oil crop rich in glucosinolates, polyunsaturated fatty acids, and antioxidants that is attracting renewed attention for its nutraceutical potential. This work aimed at investigating the therapeutic effects of a defatted seed meal (DSM) of Camelina sativa on the colon damage and the persistent visceral hypersensitivity associated with colitis in rats. Inflammation was induced by the intrarectal injection of 2,4-dinitrobenzenesulfonic acid (DNBS). The acute administration of Camelina sativa DSM (0.1–1 g kg−1) showed a dose-dependent pain-relieving effect in DNBS-treated rats. The efficacy of the meal was slightly enhanced after bioactivation with myrosinase, which increased isothiocyanate availability, and drastically decreased by pre-treating the animals with the selective peroxisome proliferator-activated receptor alpha (PPAR α) receptor antagonist GW6471. Repeated treatments with Camelina sativa DSM (1 g kg−1) meal counteracted the development, as well as the persistence, of visceral hyperalgesia in DNBS-treated animals by reducing the intestinal inflammatory damage and preventing enteric neuron damage. In conclusion, Camelina sativa meal might be employed as a nutraceutical tool to manage persistent abdominal pain in patients and to promote gut healing. Full article
(This article belongs to the Section Nutrition and Public Health)
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Figure 1
<p>The effect of <span class="html-italic">Camelina sativa</span> DSM acute administration on visceral pain associated with colitis in rats before and after bio-activation with myrosinase enzyme (Myr). (<b>A</b>) Experimental scheme: the behavioural test was performed 30 min after the oral administration of the <span class="html-italic">Camelina sativa</span> DSM (0.1–1 g kg<sup>−1</sup> p.o.). <span class="html-italic">Camelina sativa</span> DSM was bioactivated by adding 30 μL mL<sup>−1</sup> of myrosinase (32 U mL<sup>−1</sup>) 15 min before the administration. (<b>B</b>) Visceral sensitivity was assessed in animals by measuring the extent of the abdominal withdrawal response (AWR) to colorectal distension, carried out by applying an increasing distending stimulus on the colon walls (0.5–3 mL). Each value represents the mean ± SEM of six animals per group. ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^ <span class="html-italic">p</span> &lt; 0.05 and ^^ <span class="html-italic">p</span> &lt; 0.01 vs. DNBS + vehicle.</p>
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<p>The involvement of H<sub>2</sub>S and Kv7 potassium channels in the acute pain-relieving effects of <span class="html-italic">Camelina sativa</span> DSM. (<b>A</b>) Experimental scheme: the behavioural test was performed 30 min after the oral administration of the <span class="html-italic">Camelina sativa</span> DSM (0.1–1 g kg<sup>−1</sup> p.o.). Visceral sensitivity was assessed in animals by measuring the extent of the abdominal withdrawal response (AWR) to colorectal distension, carried out by applying an increasing distending stimulus on the colon walls (0.5–3 mL). (<b>B</b>) Oxidized glutathione (GSSG) (20 mg kg<sup>−1</sup>) was orally administered in concomitance with <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>), and the test was performed after 30 min. (<b>C</b>) The Kv7 potassium channel blocker XE991 (1 mg kg<sup>−1</sup>) was intraperitoneally administered in concomitance with <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>), and the test was performed after 30 min. Each value represents the mean ± SEM of six animals per group. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^ <span class="html-italic">p</span> &lt; 0.05 and ^^ <span class="html-italic">p</span> &lt; 0.01 vs. DNBS + vehicle. ° <span class="html-italic">p</span> &lt; 0.05 vs. DNBS + <span class="html-italic">Camelina sativa</span> DSM.</p>
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<p>The contribution of PPAR-α receptor activation to the acute pain-relieving effect of <span class="html-italic">Camelina sativa</span> DSM. (<b>A</b>) Experimental scheme: the behavioural test was performed 30 min after the oral administration of the <span class="html-italic">Camelina sativa</span> DSM (0.1–1 g kg<sup>−1</sup> p.o.). (<b>B</b>) Visceral sensitivity was assessed in animals by measuring the extent of the abdominal withdrawal response (AWR) to colorectal distension, carried out by applying an increasing distending stimulus on the colon walls (0.5–3 mL). The PPAR-α receptor antagonist GW6471 (2 mg kg<sup>−1</sup>) was intraperitoneally administered in concomitance with <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>), and the test was performed after 30 min. Each value represents the mean ± SEM of six animals per group. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^^ <span class="html-italic">p</span> &lt; 0.01 vs. DNBS + vehicle. ° <span class="html-italic">p</span> &lt; 0.05 and °° <span class="html-italic">p</span> &lt; 0.01 vs. DNBS + <span class="html-italic">Camelina sativa</span> DSM.</p>
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<p>The involvement of PPAR-Ƴ, CB1, and CB2 receptor in the acute pain-relieving effect of <span class="html-italic">Camelina sativa</span> DSM. Visceral sensitivity was assessed in animals by measuring the extent of the abdominal withdrawal response (AWR) to colorectal distension, carried out by applying an increasing distending stimulus on the colon walls (0.5–3 mL). (<b>A</b>) The PPAR-Ƴ receptor antagonist G3335 (2 mg kg<sup>−1</sup>) was intraperitoneally administered in concomitance with <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>), and the test was performed after 30 min. (<b>B</b>) CB1 and CB2 receptor antagonists (SR141716A and MC21, respectively; 10 mg kg<sup>−1</sup>) were intraperitoneally administered in concomitance with <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>), and the test was performed after 30 min. Each value represents the mean ± SEM of six animals per group. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^ <span class="html-italic">p</span> &lt; 0.05 and ^^ <span class="html-italic">p</span> &lt; 0.01 vs. DNBS + vehicle.</p>
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<p>The effects of the repeated administration of <span class="html-italic">Camelina sativa</span> DSM in DNBS-treated rats. (<b>A</b>) Experimental scheme: <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>) was administered once daily in the DNBS-treated animals, starting from the day of DNBS injection and continuing the daily treatment for 14 consecutive days. Body weight (<b>B</b>) and visceral pain threshold (<b>C</b>) were assessed on Days 8 (acute inflammatory phase) and 15 (post-inflammatory phase), 24 h after the last administration. Visceral sensitivity was assessed by measuring the extent of the abdominal withdrawal response (AWR) to colorectal distension (0.5–3 mL). Each value represents the mean ± SEM of six animals per group. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^ <span class="html-italic">p</span> &lt; 0.05 vs. DNBS + vehicle.</p>
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<p>The effects of the repeated treatment with <span class="html-italic">Camelina sativa</span> DSM on colon damage induced by DNBS in rats. <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>) was administered once daily in the DNBS-treated animals, starting from the day of DNBS injection for 14 consecutive days; then tissues were collected (Day 15). The column graphs report the colon macroscopic (<b>A</b>) and microscopic (<b>B</b>) damage score; Representative pictures of haematoxylin–eosin-stained sections of full-thickness colon (<b>C</b>). Original magnification: 4× and 10×. Each value represents the mean ± SEM of six animals per group. ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^ <span class="html-italic">p</span> &lt; 0.05 vs. DNBS + vehicle.</p>
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<p>The effects of the repeated treatment with <span class="html-italic">Camelina sativa</span> DSM on submucosal mast cell infiltration caused by DNBS. <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>) was administered once daily in the DNBS-treated animals, starting from the day of DNBS injection for 14 consecutive days, and then tissues were collected. The column graph displays the mean mast cell density per area of colonic wall (cells/field) (<b>A</b>). The panel shows pictures captured from submucosa of mast cell granules stained in purple with GIEMSA (<b>B</b>). Each value represents the mean ± SEM of six animals per group. ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^^ <span class="html-italic">p</span> &lt; 0.01 vs. DNBS. Original magnification: 40×.</p>
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<p>The neuroprotective effects of <span class="html-italic">Camelina sativa</span> DSM on the colonic myenteric plexus of DNBS-treated rats. <span class="html-italic">Camelina sativa</span> DSM (1 g kg<sup>−1</sup>) was administered once daily in the DNBS-treated animals, starting from the day of DNBS injection for 14 consecutive days, and then tissues were collected. The immunolabeling quantification of PGP 9.5 (<b>A</b>) and GFAP (<b>B</b>) with relative immunofluorescence images showing the expression of PGP 9.5 (green), GFAP (red), and DAPI (blue) in the myenteric plexus of the colon (<b>C</b>). The quantitative analysis of PGP9.5- and GFAP-related immunofluorescence intensity (arbitrary unit) was performed by collecting independent fields (4–6 for each animal) from the myenteric plexi. Results were expressed as a percentage of the control group (vehicle-treated animals). Each value represents the mean ± SEM of six animals per group. * <span class="html-italic">p</span> &lt; 0.05 vs. vehicle. ** <span class="html-italic">p</span> &lt; 0.01 vs. vehicle. ^ <span class="html-italic">p</span> &lt; 0.05 vs. DNBS + vehicle. Original magnification: 40×.</p>
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