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Search Results (11,667)

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10 pages, 895 KiB  
Article
Phosphine Sorption on Paddy Rice: Effects on Fumigation and Grain Quality Parameters
by Silvia Andréia Garibaldi Pereira, Lázaro da Costa Corrêa Cañizares, Silvia Leticia Rivero Meza, Cristiano Dietrich Ferreira, Silvia Naiane Jappe, Gustavo Heinrich Lang, Paulo Carteri Coradi and Maurício de Oliveira
Foods 2024, 13(20), 3293; https://doi.org/10.3390/foods13203293 (registering DOI) - 17 Oct 2024
Abstract
During storage, infestation by insect pests occurs, causing quantitative and qualitative losses in grains, which requires the control of these insects with phosphine gas. Rice husk has a high phosphine adsorption capacity, influencing the gas concentration during fumigation and potentially leading to inefficient [...] Read more.
During storage, infestation by insect pests occurs, causing quantitative and qualitative losses in grains, which requires the control of these insects with phosphine gas. Rice husk has a high phosphine adsorption capacity, influencing the gas concentration during fumigation and potentially leading to inefficient fumigation. Additionally, the high sorption of rice husk results in a higher residue of phosphine in the grain. Therefore, the objective of this study was to evaluate the phosphine sorption and phosphine residue in rice husk, paddy rice, and brown rice, as well as the industrial quality (head rice yield, rehydration capacity, cooking time, colorimetric profile) of brown and white rice during storage. To achieve this, fumigation of paddy rice, brown rice, and rice husks with 3.0 g·m−3 of phosphine was carried out for 240 h (recommended duration in the industry). A high sorption rate was observed in the rice husk (94.77%), paddy rice (97.61%), and, lastly, brown rice (35.17%). Due to the high sorption rate, only brown rice maintained a concentration above the recommended level for effective pest control (400 ppm for 120 h). Higher phosphine residues than permitted were observed in the rice husk (0.25 ppm). Lower rice head yields were observed in non-fumigated rice samples when analyzing the brown rice samples (66.21% for paddy rice and 65.01% for brown rice). A greater rehydration capacity was observed in fumigated samples at the beginning of storage when analyzing the brown rice samples (1.21 for paddy rice, 1.23 for brown rice), reducing the cooking time (24.00 for paddy rice, 23.80 for brown rice). More studies should be carried out to evaluate the effectiveness of fumigation on paddy rice, considering the high sorption rate of the paddy. Full article
(This article belongs to the Section Grain)
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<p>Metallic drums used for fumigation (<b>A</b>) and Silo-Chek—Canary Co device (<b>B</b>).</p>
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<p>Phosphine concentrations during fumigation.</p>
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<p>Phosphine residues after fumigation.</p>
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24 pages, 5552 KiB  
Article
Improving Simulations of Rice Growth and Nitrogen Dynamics by Assimilating Multivariable Observations into ORYZA2000 Model
by Jinmin Li, Liangsheng Shi, Jingye Han, Xiaolong Hu, Chenye Su and Shenji Li
Agronomy 2024, 14(10), 2402; https://doi.org/10.3390/agronomy14102402 (registering DOI) - 17 Oct 2024
Abstract
The prediction of crop growth and nitrogen status is essential for agricultural development and food security under climate change scenarios. Crop models are powerful tools for simulating crop growth and their responses to environmental variables, but accurately capturing the dynamic changes in crop [...] Read more.
The prediction of crop growth and nitrogen status is essential for agricultural development and food security under climate change scenarios. Crop models are powerful tools for simulating crop growth and their responses to environmental variables, but accurately capturing the dynamic changes in crop nitrogen remains a considerable challenge. Data assimilation can reduce uncertainties in crop models by integrating observations with model simulations. However, current data assimilation research is primarily focused on a limited number of observational variables, and insufficiently utilizes nitrogen observations. To address these challenges, this study developed a new multivariable data assimilation system, ORYZA-EnKF, that is capable of simultaneously integrating multivariable observations (including development stage, DVS; leaf area index, LAI; total aboveground dry matter, WAGT; and leaf nitrogen concentration, LNC). Then, the system was tested through three consecutive years of field experiments from 2021 to 2023. The results revealed that the ORYZA-EnKF model significantly improved the simulations of crop growth compared to the ORYZA2000 model. The relative root mean squared error (RRMSE) for LAI simulations decreased from 23–101% to 16–47% in the three-year experiment. Moreover, the incorporation of LNC observations enabled more accurate predictions of rice nitrogen dynamics, with RRMSE for LNC simulations reduced from 16–31% to 14–26%. And, the RRMSE decreased from 32–50% to 30–41% in the simulations of LNC under low-nitrogen conditions. The multivariable data assimilation system demonstrated its effectiveness in improving crop growth simulations and nitrogen status predictions, providing valuable insights for precision agriculture. Full article
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<p>Flowchart of the construction of the ORYZA-EnKF data assimilation system.</p>
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<p>(<b>a</b>) Location of Hengsha township, Shanghai city in China; (<b>b</b>) Location of two experiment sites (Yongfa village and Fumin village) in Hengsha Township; (<b>c</b>) Overview of 12 experimental plots in Yongfa village; (<b>d</b>) Overview of 24 experimental plots in Fumin village.</p>
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<p>Sensitivity indices of parameters in the ORYZA2000 model for rice yield under different nitrogen application scenarios: (<b>a</b>) the first-order sensitivity index and (<b>b</b>) the total sensitivity index. N0, N200, N300, and N400 refer to the total N rate of 0, 200, 300, and 400 kg N ha<sup>−1</sup>, respectively.</p>
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<p>Simulation results of rice state variables for three years by ORYZA2000 model. (<b>a1</b>–<b>a3</b>) DVS simulation results for 2021, 2022, and 2023; (<b>b1</b>–<b>b3</b>) LAI simulation results for 2021, 2022, and 2023; (<b>c1</b>–<b>c3</b>) WAGT simulation results for 2021, 2022, and 2023; (<b>d1</b>–<b>d3</b>) LNC simulation results for 2021, 2022, and 2023; and (<b>e1</b>–<b>e3</b>) Yield simulation results for 2021, 2022, and 2023.</p>
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<p>Influence of different observed variables on the ORYZA-EnKF data assimilation system. (<b>a1</b>–<b>e1</b>) Simulation results for DVS, LAI, WAGT, LNC, and yield when only DVS observations were assimilated; (<b>a2</b>–<b>e2</b>) Results when only LAI observations were assimilated; (<b>a3</b>–<b>e3</b>) Results when only WAGT observations were assimilated; (<b>a4</b>–<b>e4</b>) Results when only LNC observations were assimilated; and (<b>a5</b>–<b>e5</b>) Results when all observations were assimilated. The different columns represent the observations assimilated by ORYZA-EnKF, and the different rows are the simulation results of the model state variables. The black dots and lines refer to OSS observations; the red lines are open-loop simulation results; the thin lines in light blue are the simulation results of the different samples, and the thick lines in blue are the averages of the samples.</p>
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<p>Effects of nitrogen observation on the ORYZA-EnKF data assimilation system. (<b>a</b>–<b>e</b>) represent the simulation results for DVS, LAI, WAGT, LNC, and yield, respectively. The black dots and lines refer to OSS observations; the red lines are open-loop simulation results; the green line in Case 1 is the simulation result of all observed variables, and the blue line in Case 6 represents the result of removing the observation of leaf nitrogen content from all observed variables.</p>
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<p>Simulation of rice LNC by the ORYZA-EnKF data assimilation system. The legend is labeled with year + test field location + nitrogen application level. (<b>a1</b>–<b>a3</b>) 2021-YF; (<b>b1</b>–<b>b3</b>) 2022-YF; (<b>c1</b>–<b>c3</b>) 2023-FM.</p>
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<p>Simulation of the rice LAI by the ORYZA-EnKF data assimilation system. The legend is labeled with year + test field location + nitrogen application level. (<b>a1</b>,<b>a2</b>) 2021-YF; (<b>b1</b>,<b>b2</b>) 2022-YF; (<b>c1</b>,<b>c2</b>) 2023-FM.</p>
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<p>Simulation of WAGT by the ORYZA-EnKF data assimilation system. The legend is labeled with year + test field location + nitrogen application level. (<b>a1</b>,<b>a2</b>) 2021-YF; (<b>b1</b>,<b>b2</b>) 2022-YF; (<b>c1</b>,<b>c2</b>) 2023-FM.</p>
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14 pages, 3312 KiB  
Article
Revisiting the Evolution of Multi-Scale Structures of Starches with Different Crystalline Structures During Enzymatic Digestion
by Simin Chen, Zihui Qiu, Ying Yang, Jianfeng Wu, Wenjuan Jiao, Ying Chen and Chengzhi Jin
Foods 2024, 13(20), 3291; https://doi.org/10.3390/foods13203291 - 17 Oct 2024
Abstract
Porous starch has been created through hydrolysis by amyloglucosidase and α-amylase. However, little information is known about the precise evolution of multi-scale structures of starch during digestion. In this study, rice starch and potato starch, containing different crystalline structures, were hydrolyzed by amyloglucosidase [...] Read more.
Porous starch has been created through hydrolysis by amyloglucosidase and α-amylase. However, little information is known about the precise evolution of multi-scale structures of starch during digestion. In this study, rice starch and potato starch, containing different crystalline structures, were hydrolyzed by amyloglucosidase and α-amylase for 20 and 60 min, respectively, and their resulting structural changes were examined. The digestion process caused significant degradation of the molecular structures of rice and potato starches. In addition, the alterations in the ordered structures varied between the two starches. Rice starch exhibited porous structures, thicker crystalline lamellae as determined by small-angle X-ray scattering, and enhanced thermostability after digestion using differential scanning calorimetry. For rice starch, the extent of crystalline structures was analyzed with an X-ray diffractometer; it was found to first increase after 20 min of digestion and then decrease after 60 min of digestion. In contrast, potato starch did not display porous structures but exhibited thicker crystalline lamellae and a reduction in ordered structures after digestion. These findings suggest that it is possible to intentionally modulate the multi-scale structures of starch by controlling the digestion time, thereby providing valuable insights for the manipulation of starch functionalities. Full article
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<p>Morphology of starches. Rice/potato 20/60 refers to the corresponding starch after enzymatic digestion for 20/60 min. The red dotted circles indicate the breakdown of potato starch. The blue arrows indicate the starches that were greatly digested.</p>
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<p>Size distribution of starches.</p>
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<p>Lamellar structures of starches. (<b>A</b>), SAXS curves; (<b>B</b>), Kratky plots; (<b>C</b>) one-dimension correlation profiles.</p>
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<p>X-ray diffraction patterns of starches.</p>
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<p>Changes in the molecular structures of starches. (<b>A</b>), Normalized RI response of the SEC-RI chromatogram of whole starches (normalization was carried out using the individual RI signal of the first eluted peak at around 34–43 min as the normalization factor for each sample); (<b>B</b>), SEC weight chain-length distributions of debranched starches with normalized <span class="html-italic">R<sub>h</sub></span> signals (normalization was performed using the individual signal at Peak I as the normalization factor for each sample); (<b>C</b>), amylose content of starches (columns followed by different letters indicate the data differed significantly in digestion time within the same starch (<span class="html-italic">p &lt;</span> 0.05)).</p>
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<p>Schematic illustration of the changes in multi-scale structures of starches during enzymatic digestion. Rice starch is represented in green, while potato starch is shown in blue.</p>
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12 pages, 271 KiB  
Article
On Productiveness and Complexity in Computable Analysis Through Rice-Style Theorems for Real Functions
by Jingnan Xie, Harry B. Hunt and Richard E. Stearns
Mathematics 2024, 12(20), 3248; https://doi.org/10.3390/math12203248 - 17 Oct 2024
Abstract
This paper investigates the complexity of real functions through proof techniques inspired by formal language theory. Productiveness, which is a stronger form of non-recursive enumerability, is employed to analyze the complexity of various problems related to real functions. Our work provides a deep [...] Read more.
This paper investigates the complexity of real functions through proof techniques inspired by formal language theory. Productiveness, which is a stronger form of non-recursive enumerability, is employed to analyze the complexity of various problems related to real functions. Our work provides a deep reexamination of Hilbert’s tenth problem and the equivalence to the identically 0 function problem, extending the undecidability results of these problems into the realm of productiveness. Additionally, we study the complexity of the equivalence to the identically 0 function problem over different domains. We then construct highly efficient many-one reductions to establish Rice-style theorems for the study of real functions. Specifically, we show that many predicates, including those related to continuity, differentiability, uniform continuity, right and left differentiability, semi-differentiability, and continuous differentiability, are as hard as the equivalence to the identically 0 function problem. Due to their high efficiency, these reductions preserve nearly any level of complexity, allowing us to address both complexity and productiveness results simultaneously. By demonstrating these results, which highlight a more nuanced and potentially more intriguing aspect of real function theory, we provide new insights into how various properties of real functions can be analyzed. Full article
(This article belongs to the Section Mathematics and Computer Science)
15 pages, 4552 KiB  
Article
Non-Destructive Measurement of Rice Spikelet Size Based on Panicle Structure Using Deep Learning Method
by Ruoling Deng, Weisen Liu, Haitao Liu, Qiang Liu, Jing Zhang and Mingxin Hou
Agronomy 2024, 14(10), 2398; https://doi.org/10.3390/agronomy14102398 - 17 Oct 2024
Abstract
Rice spikelet size, spikelet length and spikelet width, are very important traits directly related to a rice crop’s yield. The accurate measurement of these parameters is quite significant in research such as breeding, yield evaluation and variety improvement for rice crops. Traditional measurement [...] Read more.
Rice spikelet size, spikelet length and spikelet width, are very important traits directly related to a rice crop’s yield. The accurate measurement of these parameters is quite significant in research such as breeding, yield evaluation and variety improvement for rice crops. Traditional measurement methods still mainly rely on manual labor, which is time-consuming, labor-intensive and error-prone. In this study, a novel method, dubbed the “SSM-Method”, based on convolutional neural network and traditional image processing technology has been developed for the efficient and precise measurement of rice spikelet size parameters on rice panicle structures. Firstly, primary branch images of rice panicles were collected at the same height to build an image database. The spikelet detection model using convolutional neural network was then established for spikelet recognition and localization. Subsequently, the calibration value was obtained through traditional image processing technology. Finally, the “SSM-Method” integrated with a spikelet detection model and calibration value was developed for the automatic measurement of spikelet sizes. The performance of the developed SSM-Method was evaluated through testing 60 primary branch images. The test results showed that the root mean square error (RMSE) of spikelet length for two rice varieties (Huahang15 and Qingyang) were 0.26 mm and 0.30 mm, respectively, while the corresponding RMSE of spikelet width was 0.27 mm and 0.31 mm, respectively. The proposed algorithm can provide an effective, convenient and low-cost tool for yield evaluation and breeding research. Full article
(This article belongs to the Special Issue Advanced Machine Learning in Agriculture)
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<p>Illustration of SSM-Method.</p>
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<p>Illustration of the equipment for collecting rice panicle branch images.</p>
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<p>Samples of rice panicle branch for (<b>a</b>) Huahang 15 rice variety and (<b>b</b>) Qingyang rice variety.</p>
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<p>Spikelet annotation using LabelImg software (v4.5.3).</p>
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<p>Spikelets in special circumstances of (<b>a</b>) spikelet in slanted position, (<b>b</b>) spikelet with narrow side up and (<b>c</b>) spikelet that is mostly shaded at one end.</p>
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<p>FPN structure.</p>
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<p>Structure of spikelet detection model.</p>
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<p>Single spikelet reference object of (<b>a</b>) origin image and (<b>b</b>) pixel size of single spikelet.</p>
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<p>Flowchart for calculating pixel size per millimeter for spikelet reference object.</p>
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<p>Comparison of training result between SSM-Method, Deng et al. [<a href="#B31-agronomy-14-02398" class="html-bibr">31</a>], Model-1 and Model-2 for (<b>a</b>) loss curve and (<b>b</b>) accuracy curve.</p>
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<p>Measurement results of spikelet size based on SSM-Method for (<b>a</b>) Huahang 15 rice variety and (<b>b</b>) Qingyang rice variety.</p>
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<p>Schematic diagram of automatically filtering spikelets in special situations by the proposed method for (<b>a</b>) spikelets in slanted position and (<b>b</b>) spikelets in slanted position with narrow side up.</p>
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<p>Measurement accuracy of SSM-Method of (<b>a</b>) spikelet length of Huahang 15, (<b>b</b>) spikelet width of Huahang 15, (<b>c</b>) spikelet length of Qingyang and (<b>d</b>) spikelet width of Qingyang.</p>
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12 pages, 2742 KiB  
Article
Effects of OsLPR2 Gene Knockout on Rice Growth, Development, and Salt Stress Tolerance
by Ying Gu, Chengfeng Fu, Miao Zhang, Changqiang Jin, Yuqi Li, Xingyu Chen, Ruining Li, Tingting Feng, Xianzhong Huang and Hao Ai
Agriculture 2024, 14(10), 1827; https://doi.org/10.3390/agriculture14101827 - 17 Oct 2024
Viewed by 146
Abstract
Rice (Oryza sativa L.), a globally staple food crop, frequently encounters growth, developmental, and yield limitations due to phosphate deficiency. LOW PHOSPHATE ROOT1/2 (LPR1/2) are essential genes in plants that regulate primary root growth and respond [...] Read more.
Rice (Oryza sativa L.), a globally staple food crop, frequently encounters growth, developmental, and yield limitations due to phosphate deficiency. LOW PHOSPHATE ROOT1/2 (LPR1/2) are essential genes in plants that regulate primary root growth and respond to local phosphate deficiency signals under low phosphate stress. In rice, five LPR genes, designated OsLPR1OsLPR5 based on their sequence identity with AtLPR1, have been identified. OsLPR3 and OsLPR5 are specifically expressed in roots and induced by phosphate deficiency, contributing to rice growth, development, and the maintenance of phosphorus homeostasis under low phosphate stress. In contrast, OsLPR2 is uniquely expressed in shoots, suggesting it may have distinct functions compared with other family members. This study employed Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated protein 9 (CRISPR/Cas9) gene editing technology to generate oslpr2 mutant transgenic lines and subsequently investigated the effect of OsLPR2 gene knockout on rice growth, phosphate utilization, and salt stress tolerance in the seedling stage, as well as the effect of OsLPR2 gene knockout on rice development and agronomic traits in the maturation stage. The results indicated that the knockout of OsLPR2 did not significantly impact rice seedling growth or phosphate utilization, which contrasts significantly with its homologous genes, OsLPR3 and OsLPR5. However, the mutation influenced various agronomic traits at maturity, including plant height, tiller number, and seed setting rate. Moreover, the OsLPR2 mutation conferred enhanced salt stress tolerance in rice. These findings underscore the distinct roles of OsLPR2 compared with other homologous genes, establishing a foundation for further investigation into the function of the OsLPR family and the functional differentiation among its members. Full article
(This article belongs to the Section Crop Genetics, Genomics and Breeding)
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<p>Transcript level of <span class="html-italic">OsLPR2</span> under different nutrient deficiencies. Wild type rice seedlings of Nipponbare were cultivated for 7 days in complete nutrient solution (CK) or in nutrient-deficiency solution, which excluded nitrogen (−N), phosphorus (−P), potassium (−K), magnesium (−Mg), or iron (−Fe). Relative expression levels of OsLPR2 in shoot (<b>A</b>) and root (<b>B</b>) were determined via qRT-PCR. Values are presented as means ± SE (<span class="html-italic">n</span> = 3). Different letters above the bars indicate significant differences in the relative expression levels of OsLPR2 (<span class="html-italic">p</span> &lt; 0.05, one-way ANOVA).</p>
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<p>Construction and identification of <span class="html-italic">OsLPR2</span> mutant material. (<b>A</b>) Schematic diagram of the <span class="html-italic">oslpr2</span> target sites. (<b>B</b>) Identification of positive <span class="html-italic">oslpr2</span> seedlings. (<b>C</b>) Sequencing sequences and chromatograms of homozygous <span class="html-italic">oslpr2</span> mutant lines. (<b>D</b>) Cas9 segregation identification of mutant lines.</p>
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<p>The effect of <span class="html-italic">OsLPR2</span> mutation on the plant height and tillers per plant at maturity. (<b>A</b>) Plant types. (<b>B</b>) Plant height. (<b>C</b>) Number of tillers per plant. Scale bar: 20 cm. Values are means ± SE (<span class="html-italic">n</span> = 15). Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05, one-way ANOVA).</p>
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<p>The effect of <span class="html-italic">OsLPR2</span> mutation on panicle type of rice. (<b>A</b>) Panicle types. (<b>B</b>) Panicle length. (<b>C</b>) Number of primary branches. (<b>D</b>) Number of secondary branches. (<b>E</b>) Number of grains per panicle. (<b>F</b>) Seed setting rate. Scale bar: 5 cm. Values are means ± SE (<span class="html-italic">n</span> = 15). Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05, one-way ANOVA).</p>
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<p>The effect of <span class="html-italic">OsLPR2</span> mutation on the lengths of shoots and roots. (<b>A</b>,<b>B</b>) Images showing the relative growth performances of WT and <span class="html-italic">oslpr2</span> mutant lines under +P and −P conditions (bar = 10 cm). (<b>C</b>,<b>E</b>) Lengths and biomass of shoots or roots under phosphate sufficiency. (<b>D</b>,<b>F</b>) Lengths and biomass of shoots and roots under phosphate deficiency. Values are presented as means ± SE (<span class="html-italic">n</span> = 6). Same letters above the bars indicate no significant differences (<span class="html-italic">p</span> &lt; 0.05, one-way ANOVA).</p>
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<p>The effect of <span class="html-italic">OsLPR2</span> mutation on soluble Pi concentration of rice. (<b>A</b>) <span class="html-italic">OsLPR2</span> transgenic materials and wild type plants with consistent growth under normal phosphate supply. (<b>B</b>) After 21 days of phosphate deficiency treatment, sampling of different plant parts (leaves, leaf sheaths, roots) for extractable phosphate content measurement. Values are means ± SE (<span class="html-italic">n</span> = 3). Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05, one-way ANOVA).</p>
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<p>Assessment of <span class="html-italic">oslpr2</span> mutant survival and physiological responses under saline conditions. (<b>A</b>) Phenotypes of WT and <span class="html-italic">oslpr2</span> mutants after 200 mM NaCl treatment. (<b>B</b>) Survival rate statistics. (<b>C</b>) POD activity after 150 mM NaCl treatment. (<b>D</b>) MDA content after 150 mM NaCl treatment. Values are means ± SE (<span class="html-italic">n</span> = 3). Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05, one-way ANOVA).</p>
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20 pages, 7114 KiB  
Article
The Synergistic Effect of Limestone Powder and Rice Husk Ash on the Mechanical Properties of Cement-Based Materials
by Jialei Wang, Feifei Jiang, Juan Zhou and Zhongyang Mao
Materials 2024, 17(20), 5058; https://doi.org/10.3390/ma17205058 - 16 Oct 2024
Viewed by 317
Abstract
Fully utilizing solid waste as supplementary cementitious materials (SCMs) while ensuring the mechanical properties of cement-based materials is one of the pathways for carbon reduction in the cement industry. Understanding the effects of the two solid wastes-limestone powder (LP) and rice husk ash [...] Read more.
Fully utilizing solid waste as supplementary cementitious materials (SCMs) while ensuring the mechanical properties of cement-based materials is one of the pathways for carbon reduction in the cement industry. Understanding the effects of the two solid wastes-limestone powder (LP) and rice husk ash (RHA) on the mechanical properties of cement-based materials is of great significance for their application in concrete. This study investigates the impact of LP and RHA on the strength of cement mortar at various ages and the microhardness of hardened cement paste. The results suggest that two materials have a certain synergistic effect on the mechanical properties of the cementitious materials. The addition of RHA effectively addresses the issues of slow strength development, insufficient late-stage strength of the cementitious material, and the low strength blended with a large amount of LP, while a suitable amount of LP can promote the strength increase in the cement-RHA system. Based on the comprehensive analysis of compressive strength and microhardness, the optimal solution for achieving high mechanical properties in composite cementitious materials is to use 10% each of LP and RHA, resulting in a 9.5% increase in 28 d strength compared to a pure cement system. The higher the content of LP, the greater the increase caused by 10% RHA in compressive strength of the composite system, which makes the strength growth rate of cementitious material mixed with 10% LP at 3–56 d 62.1%. When the LP content is 20% and 30%, the addition of 10% RHA increases the 28 d strength by 44.8% and 38.8%, respectively, with strength growth rates reaching 109.8% and 151.1% at 3–56 d. Full article
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<p>Combustion program and preparation process of RHA.</p>
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<p>The (<b>a</b>) particle size distribution and (<b>b</b>) particle parameters of cement, LP, and RHA.</p>
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<p>Characterization of pore structure characteristics of RHA.</p>
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<p>SEM images (<b>a</b>) ×500 and (<b>b</b>) ×4000 of RHA.</p>
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<p>Compressive and flexural strength tests of cement mortar.</p>
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<p>Indentation lattice of microhardness.</p>
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<p>Effect of RHA on (<b>a</b>) compressive strength and (<b>b</b>) flexural strength of cement mortar.</p>
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<p>Effect of RHA on (<b>a</b>,<b>c</b>) compressive strength and (<b>b</b>,<b>d</b>) flexural strength of cement-LP composite mortar.</p>
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<p>Effect of RHA on compressive strength growth rate of cement-LP mortar.</p>
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<p>Effect of LP on (<b>a</b>) compressive strength and (<b>b</b>) flexural strength of cement mortar.</p>
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<p>Effect of LP on (<b>a</b>) compressive strength and (<b>b</b>) flexural strength of cement-RHA mortar.</p>
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<p>Effect of LP and RHA on compressive strength (<b>a</b>) 3 d, (<b>b</b>) 7 d, (<b>c</b>) 28 d, and (<b>d</b>) 56 d in composite system.</p>
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<p>Effect of LP and RHA on compressive strength (<b>a</b>) 3 d, (<b>b</b>) 7 d, (<b>c</b>) 28 d, and (<b>d</b>) 56 d in composite system.</p>
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<p>Microhardness of cement-LP-RHA composite paste.</p>
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<p>Probability distribution of composite paste microhardness in (<b>a</b>) cement-LP, (<b>b</b>) cement-RHA and (<b>c</b>,<b>d</b>) cement-LP-RHA system.</p>
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<p>Box-plot of microhardness distribution of hardened cement paste.</p>
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<p>Fitting of microhardness data with different distributions (<b>a</b>) normal, (<b>b</b>) 3-Parameter Lognormal, (<b>c</b>) 3-Parameter Weibull, and (<b>d</b>) 3-Parameter Gamma of samples.</p>
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<p>Probability density of 3-Parameter Lognormal distribution of microhardness data in (<b>a</b>) cement-LP, (<b>b</b>) cement-RHA and (<b>c</b>,<b>d</b>) cement-LP-RHA system.</p>
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<p>Comparison of compressive strength and statistical parameters of microhardness in (<b>a</b>) cement-LP, (<b>b</b>) cement-RHA and (<b>c</b>,<b>d</b>) cement-LP-RHA system.</p>
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15 pages, 1942 KiB  
Article
Role of Nitrogen Fertilization and Sowing Date in Productivity and Climate Change Adaptation Forecast in Rice–Wheat Cropping System
by Khalid Hussain, Erdoğan Eşref Hakki, Ayesha Ilyas, Sait Gezgin and Muhammad Asif Kamran
Nitrogen 2024, 5(4), 977-991; https://doi.org/10.3390/nitrogen5040062 (registering DOI) - 16 Oct 2024
Viewed by 208
Abstract
Global food security is at risk due to climate change. Soil fertility loss is among the impacts of climate change which reduces the productivity of rice–wheat cropping systems. This study investigated the effects of varying nitrogen levels and transplanting/sowing dates on the grain [...] Read more.
Global food security is at risk due to climate change. Soil fertility loss is among the impacts of climate change which reduces the productivity of rice–wheat cropping systems. This study investigated the effects of varying nitrogen levels and transplanting/sowing dates on the grain yield (GY) and biological yield (BY) of rice and wheat cultivars over two growing seasons (2017–2019). Additionally, the impact of climate change on the productivity of both crops was tested under a 1.5 °C temperature increase and 510 ppm CO2 concentration while nitrogen fertilization and sowing window adjustments were evaluated as adaptation options using the DSSAT and APSIM models. Results indicated that the application of 120 kg N ha−1 significantly enhanced both GY and BY in all rice cultivars. The highest wheat yields were obtained with 140 kg N ha−1 for all cultivars. Rice transplanting on the 1st of July and wheat sowing on the 15th of November showed the best yields. The statistical indices of the model’s forecast results were satisfactory for rice (R2 = 0.83–0.85, root mean square error (RMSE) = 341–441, model efficiency (EF) = 0.82–0.89) and wheat (R2 = 0.84–0.89, RMSE = 213–303, EF = 0.88–0.91). Both models predicted yield loss in wheat (20–25%) and rice (28–30%) under a climate change scenario. The models also predicted that increased nitrogen application and earlier planting would be necessary to reduce the impacts of climate change on the productivity of both crops. Full article
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<p>Relationships between modeled and measured rice grain yield during (<b>a</b>) DSSAT calibration, (<b>b</b>) DSSAT evaluation (<b>c</b>) APSIM calibration and (<b>d</b>) APSIM evaluation.</p>
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<p>Climate change impact assessment and adaptation strategies in three high-yielding rice cultivars at baseline (2017–2018 conditions), Scenario 1 (+1.5 °C with 510 ppm CO<sub>2</sub>), Scenario 2 (Scenario 1 with 10% fertilizer increase), Scenario 3 (Scenario 1 with 10 days earlier sowing) by using (<b>a</b>) DSSAT and (<b>b</b>) APSIM after calibration and evaluation. Standard error is presented as error bars.</p>
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<p>Climate change impact assessment and adaptation strategies in three high-yielding wheat cultivars at baseline (2017–2018 conditions), Scenario 1 (+1.5 °C with 510 ppm CO<sub>2</sub>), Scenario 2 (Scenario 1 with 10% fertilizer increase), Scenario 3 (Scenario 1 with 15 days earlier transplanting) by using (<b>a</b>) DSSAT and (<b>b</b>) APSIM after calibration and evaluation. Standard error is presented as error bars.</p>
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26 pages, 2170 KiB  
Review
Advancements in Bacteriophages for the Fire Blight Pathogen Erwinia amylovora
by Dufang Ke, Jinyan Luo, Pengfei Liu, Linfei Shou, Munazza Ijaz, Temoor Ahmed, Muhammad Shafiq Shahid, Qianli An, Ivan Mustać, Gabrijel Ondrasek, Yanli Wang, Bin Li and Binggan Lou
Viruses 2024, 16(10), 1619; https://doi.org/10.3390/v16101619 (registering DOI) - 16 Oct 2024
Viewed by 321
Abstract
Erwinia amylovora, the causative agent of fire blight, causes significant economic losses for farmers worldwide by inflicting severe damage to the production and quality of plants in the Rosaceae family. Historically, fire blight control has primarily relied on the application of copper [...] Read more.
Erwinia amylovora, the causative agent of fire blight, causes significant economic losses for farmers worldwide by inflicting severe damage to the production and quality of plants in the Rosaceae family. Historically, fire blight control has primarily relied on the application of copper compounds and antibiotics, such as streptomycin. However, the emergence of antibiotic-resistant strains and growing environmental concerns have highlighted the need for alternative control methods. Recently, there has been a growing interest in adopting bacteriophages (phages) as a biological control strategy. Phages have demonstrated efficacy against the bacterial plant pathogen E. amylovora, including strains that have developed antibiotic resistance. The advantages of phage therapy includes its minimal impact on microbial community equilibrium, the lack of a detrimental impact on plants and beneficial microorganisms, and its capacity to eradicate drug-resistant bacteria. This review addresses recent advances in the isolation and characterization of E. amylovora phages, including their morphology, host range, lysis exertion, genomic characterization, and lysis mechanisms. Furthermore, this review evaluates the environmental tolerance of E. amylovora phages. Despite their potential, E. amylovora phages face certain challenges in practical applications, including stability issues and the risk of lysogenic conversion. This comprehensive review examines the latest developments in the application of phages for controlling fire blight and highlights the potential of E. amylovora phages in plant protection strategies. Full article
(This article belongs to the Section Bacterial Viruses)
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<p>Distribution of phages from various families infecting <span class="html-italic">E. amylovora</span> and <span class="html-italic">E. pyrifoliae</span> in different countries. The stacked bar chart was constructed utilizing Chiplot (<a href="https://www.chiplot.online/" target="_blank">https://www.chiplot.online/</a>; accessed on 22 August 2024).</p>
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<p>This phylogenetic tree of <span class="html-italic">E. amylovora</span> phages was constructed with MEGA 7.0 software by using the maximum composite likelihood method based on the terminase large subunit available in published articles. Nodes show the result of 500 bootstrap replicates.</p>
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<p>The figure illustrates an integrated control strategy based on a phage–carrier system and phage cocktail approach. (<b>A</b>) Different phages binding to vector bacteria; (<b>B</b>) phage infestation of vectors; and (<b>C</b>) phage release. The strategy employs a combination of three key elements: phages, UV protectants, and an auxiliary formulation.</p>
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11 pages, 2073 KiB  
Article
Polylactide-Based Polymer Composites with Rice Husk Filler
by Roman Aleksandrovich Lyubushkin, Natalia Igorevna Cherkashina, Daria Vasilievna Pushkarskaya, Elena Vitalievna Forova, Artem Yuryevich Ruchiy and Semyon Nikolaevich Domarev
J. Compos. Sci. 2024, 8(10), 427; https://doi.org/10.3390/jcs8100427 (registering DOI) - 16 Oct 2024
Viewed by 188
Abstract
In this work, composites made of polylactide (PLA) and filled with alkali-pretreated rice husk (RH) were investigated. Composites containing 20, 30, and 40 wt.% of RH were synthesized. It was shown that alkaline treatment, along with the change in crystal lattice, led to [...] Read more.
In this work, composites made of polylactide (PLA) and filled with alkali-pretreated rice husk (RH) were investigated. Composites containing 20, 30, and 40 wt.% of RH were synthesized. It was shown that alkaline treatment, along with the change in crystal lattice, led to an increase in the content of non-crystalline parts and the volume of intercrystalline spaces, and the internal surface of the cellulose fiber increased, which resulted in improved adhesion of the fiber with the matrix. The addition of rice husk to the PLA matrix led to an increase in the flexural modulus, which increased to 2881 MPa for the PLA/RH (80/20 wt.%) and 3034 MPa for the PLA/RH (70/30 wt.%) composites and lowered the peak load stress by approximately 43% for the composite with 20 wt.% RH and 56% for the composite with 30 wt.% RH. The reduction in the degree of PLA crystallinity allows macromolecules to move more freely in amorphous regions, which has a positive effect on increasing the flexibility of materials in general. The optimal formulation is a composite consisting of 30% RH and 70% PLA matrix. Full article
(This article belongs to the Section Polymer Composites)
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<p>Morphology (<b>a</b>) and size distribution (<b>b</b>) of alkali-treated RH particles after milling.</p>
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<p>FTIR spectra of untreated and alkaline-treated RHs.</p>
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<p>XRD patterns of untreated and alkaline-treated rice husks.</p>
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<p>Thermal stability of PLA (<b>a</b>), alkaline-treated RH (<b>b</b>), and the composite based on them (<b>c</b>) (PLA 60%-RH40%).</p>
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<p>Weight increase in pure PLA and its composites (20%, 30%, and 40% RH immersed in saline solution at 40 °C).</p>
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22 pages, 14941 KiB  
Article
Profiling of Key Hub Genes Using a Two-State Weighted Gene Co-Expression Network of ‘Jao Khao’ Rice under Soil Salinity Stress Based on Time-Series Transcriptome Data
by Prasit Khunsanit, Kitiporn Plaimas, Supachitra Chadchawan and Teerapong Buaboocha
Int. J. Mol. Sci. 2024, 25(20), 11086; https://doi.org/10.3390/ijms252011086 (registering DOI) - 16 Oct 2024
Viewed by 274
Abstract
RNA-sequencing enables the comprehensive detection of gene expression levels at specific time points and facilitates the identification of stress-related genes through co-expression network analysis. Understanding the molecular mechanisms and identifying key genes associated with salt tolerance is crucial for developing rice varieties that [...] Read more.
RNA-sequencing enables the comprehensive detection of gene expression levels at specific time points and facilitates the identification of stress-related genes through co-expression network analysis. Understanding the molecular mechanisms and identifying key genes associated with salt tolerance is crucial for developing rice varieties that can thrive in saline environments, particularly in regions affected by soil salinization. In this study, we conducted an RNA-sequencing-based time-course transcriptome analysis of ‘Jao Khao’, a salt-tolerant Thai rice variety, grown under normal or saline (160 mM NaCl) soil conditions. Leaf samples were collected at 0, 3, 6, 12, 24, and 48 h. In total, 36 RNA libraries were sequenced. ‘Jao Khao’ was found to be highly salt-tolerant, as indicated by the non-significant differences in relative water content, cell membrane stability, leaf greenness, and chlorophyll fluorescence over a 9-day period under saline conditions. Plant growth was slightly retarded during days 3–6 but recovered by day 9. Based on time-series transcriptome data, we conducted differential gene expression and weighted gene co-expression network analyses. Through centrality change from normal to salinity network, 111 key hub genes were identified among 1,950 highly variable genes. Enriched genes were involved in ATP-driven transport, light reactions and response to light, ATP synthesis and carbon fixation, disease resistance and proteinase inhibitor activity. These genes were upregulated early during salt stress and RT-qPCR showed that ‘Jao Khao’ exhibited an early upregulation trend of two important genes in energy metabolism: RuBisCo (LOC_Os10g21268) and ATP synthase (LOC_Os10g21264). Our findings highlight the importance of managing energy requirements in the initial phase of the plant salt-stress response. Therefore, manipulation of the energy metabolism should be the focus in plant resistance breeding and the genes identified in this work can serve as potentially effective candidates. Full article
(This article belongs to the Special Issue Abiotic Stress Tolerance and Genetic Diversity in Plants, 2nd Edition)
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<p>Comparison of phenotypic traits between normal and saline conditions of ‘Jao Khao’. (<b>A</b>) tiller number, (<b>B</b>) SES, (<b>C</b>) shoot fresh weight, (<b>D</b>) root fresh weight, (<b>E</b>) shoot dry weight, (<b>F</b>) root dry weight, (<b>G</b>) shoot dry-to-fresh weight ratio, (<b>H</b>) root dry-to-fresh weight ratio, (<b>I</b>) CMS, and (<b>J</b>) RWC. Data are presented as means ± SD (n = 3). Statistical significance was determined using the Duncan multiple range test. Significant differences (<span class="html-italic">p</span> ≤ 0.05) are indicated by different letters. ns: not significant.</p>
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<p>Leaf greenness and chlorophyll fluorescence of ‘Jao Khao’ compared between that of control and salt conditions. (<b>A</b>) SPAD index, (<b>B</b>) Maximum PSII efficiency (Fv/Fm), and (<b>C</b>) Performance index (Pi). Data are presented as means ± SD (n = 3). Statistical significance was determined using the Duncan multiple range test. Significant differences (<span class="html-italic">p</span> ≤ 0.05) are indicated by different letters. ns: not significant.</p>
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<p>Normalized read counts of 36 RNA-sequencing library (<b>A</b>), scale-free topology and mean connectivity (the horizontal red line was at <span class="html-italic">R</span><sup>2</sup> = 0.9) (<b>B</b>), the heatmap of topological overlapping matrix (TOM) plot visualizing the strength of the connections (similarity) between genes with the bright yellow color indicating genes with more connections or shared neighbors in the network and the colors representing modules displayed on both axes (<b>C</b>), and module–trait relationships (MTR) (<b>D</b>). The colors of modules include blue, red, turquoise, green, brown, yellow and grey. The letters ct and ss indicate control conditions and salt stress conditions, respectively. ME: Module Eigengene, a representative of gene expression levels in a cluster of co-expressed genes. Significant differences (<span class="html-italic">p</span> ≤ 0.05) are indicated by *.</p>
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<p>Comparison of the distribution of centrality between the normal-state and saline-state networks for (<b>A</b>) degree, (<b>B</b>) closeness, (<b>C</b>) betweenness, and (<b>D</b>) the clustering coefficient.</p>
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<p>Gene Ontology (GO) enrichment analysis results for each module. <span class="html-italic">p</span>-values were adjusted using the Benjamini–Hochberg correction. (<b>A</b>) Brown module, (<b>B</b>) turquoise module, (<b>C</b>) yellow module, (<b>D</b>) blue module, (<b>E</b>) red module, and (<b>F</b>) green module. GO terms include biological process (BP), cellular component (CC), and molecular function (MF).</p>
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<p>Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment results for each module. <span class="html-italic">p</span>-values were adjusted using the Benjamini–Hochberg correction.</p>
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<p>Gene networks and key genes were identified based on the centrality change between the two states (normal and saline) and mapped to the global state network. (<b>A</b>) Brown module, (<b>B</b>) turquoise module, (<b>C</b>) yellow module, (<b>D</b>) blue module, (<b>E</b>) red module, (<b>F</b>) green module, and (<b>G</b>) grey module. Small nodes and edges are colored according to the module they belong to. Large nodes represent key genes detected based on DG, BW, CN, and CC centrality, with combinations of 1, 2, 3, and 4 centrality measures, which are indicated in bright colors: green, blue, orange, and red, respectively.</p>
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<p>Relative expression levels (fold change) of two genes involved in energy metabolism: <span class="html-italic">LOC_Os10g21268</span> and <span class="html-italic">LOC_Os10g21264</span> in three varieties: ‘Jao Khao’ (<b>A</b>,<b>D</b>), ‘Pokkali’ (<b>B</b>,<b>E</b>), and ‘IR29’ (<b>C</b>,<b>F</b>) grown under salt stress conditions relative to those under control conditions by RT-qPCR. Data are presented as means ± SD (<span class="html-italic">n</span> = 3). Statistical significance was determined using the Duncan multiple range test. Significant differences (<span class="html-italic">p</span> ≤ 0.05) are indicated by different letters.</p>
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<p>Proposed mechanism of salt stress responses in ‘Jao Khao’ rice as inferred from a comprehensive analysis of time-course transcriptome data. Names bordered by colored lines are key genes. Transcription factors are shown in red letters. GO enrichment analysis revealed several GO terms related to key plant energy metabolism processes, such as light reactions, carbon fixation, and ATP synthesis. Many genes associated with these GO terms exhibited increased expression under salt stress. These enriched processes indicate the importance of maintaining energy production early during salt stress to regulate ion and water uptake and transport. Other enriched GO terms suggested the involvement of ATP-driven transport and the ubiquitination-proteasome pathway in responses to salt stress. Several candidate transcription factors, including <span class="html-italic">bZIP46</span>, <span class="html-italic">SPL4</span>, <span class="html-italic">ASR5</span>, and the transcriptional corepressor LEUNIG, may coordinate these processes. Dash-arrows and question marks suggest potential regulatory relationships.</p>
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<p>Diagram illustrating the co-expression network analysis pipeline used in the present study.</p>
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17 pages, 1263 KiB  
Article
Differences in Grain Yield and Nitrogen Uptake between Tetraploid and Diploid Rice: The Physiological Mechanisms under Field Conditions
by Jian Xiao, Zhuang Xiong, Jiada Huang, Zuolin Zhang, Detian Cai, Dongliang Xiong, Kehui Cui, Shaobing Peng and Jianliang Huang
Plants 2024, 13(20), 2884; https://doi.org/10.3390/plants13202884 (registering DOI) - 15 Oct 2024
Viewed by 303
Abstract
Research indicates that, owing to the enhanced grain-filling rate of tetraploid rice, its yield has notably improved compared to previous levels. Studies conducted on diploid rice have revealed that optimal planting density and fertilization rates play crucial roles in regulating rice yield. In [...] Read more.
Research indicates that, owing to the enhanced grain-filling rate of tetraploid rice, its yield has notably improved compared to previous levels. Studies conducted on diploid rice have revealed that optimal planting density and fertilization rates play crucial roles in regulating rice yield. In this study, we investigated the effects of different nitrogen application and planting density treatments on the growth, development, yield, and nitrogen utilization in tetraploid (represented by T7, an indica–japonica conventional allotetraploid rice) and diploid rice (Fengliangyou-4, represented by FLY4, a two-line super hybrid rice used as a reference variety for the approval of super rice with a good grain yield performance). The results indicated that the highest grain-filling rate of T7 could reach 77.8% under field experimental conditions due to advancements in tetraploid rice breeding. This is a significant improvement compared with the rate seen in previous research. Under the same conditions, T7 exhibited a significantly lower grain yield than FLY4, which could be attributed to its lower grain-filling rate, spikelets per panicle, panicle number m−2, and harvest index score. Nitrogen application and planting density displayed little effect on the grain yield of both genotypes. A higher planting density significantly enhanced the leaf area index and biomass accumulation, but decreased the harvest index score. Compared with T7, FLY4 exhibited a significantly higher nitrogen use efficiency (NUEg), which was mainly due to the higher nitrogen content in the straw. Increasing nitrogen application significantly decreased NUEg due to its minimal effect on grain yield combined with its significant enhancement of nitrogen uptake. Our results suggest that the yield and grain-filling rate of T7 have been improved compared with those of previously tested polyploid rice, but are still lower than those of FLY4, and the yield of tetraploid rice can be further improved by enhancing the grain-filling rate, panicle number m−2, and spikelets per panicle via genotype improvement. Full article
(This article belongs to the Special Issue Emerging Trends in Alternative and Sustainable Crop Production)
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<p>Effects of different planting density and nitrogen application treatments on grain yield in tetraploid T7 and diploid FLY4 rice in 2018 (<b>a</b>) and 2019 (<b>b</b>). The error bar indicates SE (<span class="html-italic">n</span> = 3). Within a group of the same genotypes, different letters indicate significant differences according to LSD (0.05). T7: tetraploid rice; FLY4: Fengliangyou-4. TD17: lower-density treatment (20.0 cm × 30.0 cm), 16.7 hills per m<sup>−2</sup>; TD25: high-density treatment (13.3 cm × 30.0 cm), 25 hills per m<sup>−2</sup>. N1: N rate 150 kg ha<sup>−1</sup>; N2: N rate 225 kg ha<sup>−1</sup>; N3: N rate 300 kg ha<sup>−1</sup>. N1TD25, N1TD17, N2TD25, N2TD17, N3TD25, and N3TD17 represent different combinations of N application rates and density treatments.</p>
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<p>Changes in tillering dynamics in tetraploid T7 (<b>a</b>,<b>c</b>) and diploid FLY4 (<b>b</b>,<b>d</b>) under different densities and nitrogen application treatments in 2018 (<b>a</b>,<b>b</b>) and 2019 (<b>c</b>,<b>d</b>). The error bar indicates SE (<span class="html-italic">n</span> = 3). The red arrow indicates the time point of the panicle initiation stage. TD17: lower-density treatment (20.0 cm × 30.0 cm), 16.7 hills per m<sup>−2</sup>; TD25: high-density treatment (13.3 cm × 30.0 cm), 25 hills per m<sup>−2</sup>. N1: N rate 150 kg ha<sup>−1</sup>; N2: N rate 225 kg ha<sup>−1</sup>; N3: N rate 300 kg ha<sup>−1</sup>. N1TD25, N1TD17, N2TD25, N2TD17, N3TD25 and N3TD17 represent different combinations of N application rates and density treatments.</p>
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<p>Effects of different planting density and nitrogen application treatments on leaf area index in tetraploid T7 (<b>a</b>,<b>c</b>) and diploid FLY4 (<b>b</b>,<b>d</b>) in 2018 (<b>a</b>,<b>b</b>) and 2019 (<b>c</b>,<b>d</b>). Error bar indicates SE (<span class="html-italic">n</span> = 3). Within a group of the same genotypes, different letters indicate significant differences according to LSD (0.05). TD17: lower-density treatment (20.0 cm × 30.0 cm), 16.7 hills per m<sup>−2</sup>; TD25: high-density treatment (13.3 cm × 30.0 cm), 25 hills per m<sup>−2</sup>. N1: N rate 150 kg ha<sup>−1</sup>; N2: N rate 225 kg ha<sup>−1</sup>; N3: N rate 300 kg ha<sup>−1</sup>. N1TD25, N1TD17, N2TD25, N2TD17, N3TD25 and N3TD17 represent different combinations of N application rates and density treatments. PI: panicle initiation stage approximately 32 days after transplanting; HD: heading stage approximately 63 days after transplanting.</p>
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<p>Effects of different planting density and nitrogen application treatments on biomass in tetraploid T7 (<b>a</b>,<b>c</b>) and diploid FLY4 (<b>b</b>,<b>d</b>) in 2018 (<b>a</b>,<b>b</b>) and 2019 (<b>c</b>,<b>d</b>). The error bar indicates SE (<span class="html-italic">n</span> = 3). Within a group of the same genotypes, different letters indicate significant differences according to LSD (0.05). TD17: lower-density treatments (20.0 cm × 30.0 cm), 16.7 hills per m<sup>−2</sup>; TD25: high-density treatments (13.3 cm × 30.0 cm), 25 hills per m<sup>−2</sup>. N1: N rate 150 kg ha<sup>−1</sup>; N2: N rate 225 kg ha<sup>−1</sup>; N3: N rate 300 kg ha<sup>−1</sup>. N1TD25, N1TD17, N2TD25, N2TD17, N3TD25 and N3TD17 represent different combinations of N application rates and density treatments. PI: panicle initiation stage approximately 32 days after transplanting; HD: heading stage approximately 63 days after transplanting; MA: approximately 104 days after transplanting.</p>
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<p>Effects of different treatments on the SPAD value of the flag leaf in tetraploid T7 (<b>a</b>,<b>c</b>) and diploid FLY4 (<b>b</b>,<b>d</b>) at HD and 21 days after HD stage in 2018 (<b>a</b>,<b>b</b>) and 2019 (<b>c</b>,<b>d</b>). The error bar indicates SE (<span class="html-italic">n</span> = 3). In a set of bar charts of the same color, different letters indicate significant differences according to LSD (0.05). Lower-case letters indicate comparisons among different treatments within each group. The content in the legend represents measurement time at HD (approximately 63 days after transplanting) and 21 days after the HD stage. TD17: lower-density treatment (20.0 cm × 30.0 cm), 16.7 hills per m<sup>−2</sup>; TD25: high-density treatment (13.3 cm × 30.0 cm), 25 hills per m<sup>−2</sup>. N1: N rate 150 kg ha<sup>−1</sup>; N2: N rate 225 kg ha<sup>−1</sup>; N3: N rate 300 kg ha<sup>−1</sup>. N1TD25, N1TD17, N2TD25, N2TD17, N3TD25 and N3TD17 represent different combinations of N application rates and density treatments.</p>
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16 pages, 6874 KiB  
Article
Genome-Wide Identification of the RALF Gene Family and Expression Pattern Analysis in Zea mays (L.) under Abiotic Stresses
by Baoping Xue, Zicong Liang, Yue Liu, Dongyang Li and Chang Liu
Plants 2024, 13(20), 2883; https://doi.org/10.3390/plants13202883 (registering DOI) - 15 Oct 2024
Viewed by 353
Abstract
Rapid Alkalization Factor (RALF) is a signaling molecule in plants that plays a crucial role in growth and development, reproductive processes, and responses to both biotic and abiotic stresses. Although RALF peptides have been characterized in Arabidopsis and rice, a comprehensive bioinformatics analysis [...] Read more.
Rapid Alkalization Factor (RALF) is a signaling molecule in plants that plays a crucial role in growth and development, reproductive processes, and responses to both biotic and abiotic stresses. Although RALF peptides have been characterized in Arabidopsis and rice, a comprehensive bioinformatics analysis of the ZmRALF gene family in maize is still lacking. In this study, we identified 20 RALF genes in the maize genome. Sequence alignment revealed significant structural variation among the ZmRALF family genes. Phylogenetic analysis indicates that RALF proteins from Arabidopsis, rice, and maize can be classified into four distinct clades. Duplication events suggest that the expansion of the RALF gene family in maize primarily relies on whole-genome duplication. ZmRALF genes are widely expressed across various tissues; ZmRALF1/15/18/19 are highly expressed in roots, while ZmRALF6/11/14/16 are predominantly expressed in anthers. RNA-seq and RT-qPCR demonstrated that the expression levels of ZmRALF7, ZmRALF9, and ZmRALF13 were significantly up-regulated and down-regulated in response to PEG and NaCl stresses, respectively. Overall, our study provides new insights into the role of the RALF gene family in abiotic stress. Full article
(This article belongs to the Collection Exploration and Application of Useful Agricultural Genes)
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<p>Chromosome distribution of <span class="html-italic">ZmRALF</span> genes. The distribution of 20 <span class="html-italic">ZmRALFs</span> genes on ten maize chromosomes.</p>
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<p>Multiple sequence alignment of ZmRALF proteins. Multiple sequence alignment was carried out using DNAman 8. The red triangles represent cysteine residues. The scissors represent the RRXL protease recognition site. The first red box represents the RRXL cleavage site and the second red box represents the YISY conserved motif. The blue lines represent GASYY conserved motif.</p>
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<p>Phylogenetic tree of 133 proteins from ZmRALF, AtRALF, SiRALF, SbRALF, and OsRALF proteins. These protein sequences were aligned using MUSCLE, then a phylogenetic tree was constructed using the neighbor-joining (N-J) method with 1000 bootstraps in MEGA 7.0. The picture was created with the online tool iTOL 6.9.1 (<a href="https://itol.embl.de/" target="_blank">https://itol.embl.de/</a>, accessed on 20 July 2024). Different colors indicate different RALF subgroups.</p>
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<p>The gene structure and protein conserved motifs of ZmRALF. (<b>A</b>) The phylogenetic tree was constructed using MEGA 7.0 software (method: neighbor-joining; bootstrap: 1000). (<b>B</b>) The gene structure was analyzed using GFF files. (<b>C</b>) Protein conserved motifs were analyzed by MEME. (<b>D</b>) Protein sequence analysis of ZmRALF motifs.</p>
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<p>The duplication events analysis of <span class="html-italic">ZmRALF</span> genes. Names in red name represent tandem replication genes, while blue lines represent whole-genome duplication genes.</p>
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<p>Collinear gene pair analysis of <span class="html-italic">ZmRALF</span> between maize and rice and <span class="html-italic">Arabidopsis</span>. The blue line represents collinear gene pairs. The pink color represents the maize chromosome, the green represents the rice chromosome, and the purple represents the <span class="html-italic">Arabidopsis</span> chromosome.</p>
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<p>Analysis of cis-elements of <span class="html-italic">ZmRALF</span> gene promoter sequences. (<b>A</b>) This evolutionary tree was generated by MEGA 7.0 software (method: neighbor-joining; bootstrap: 1000). (<b>B</b>) Cis-elements in the 2 kb promoter sequences of <span class="html-italic">ZmRALF</span> genes were predicted. These cis-elements include hormone-related, abiotic and biotic-related, growth and development-related, light-related, and transcription factor binding sites-related.</p>
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<p>The tissue expression pattern of <span class="html-italic">ZmRALF</span> genes in different tissues including root, endosperm, leaf base, ear, embryo, anther, leaf tip, shoot, and leaf. Red and blue boxes indicate high and low expression levels of <span class="html-italic">ZmRALF</span> genes.</p>
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<p>The expression pattern analysis of <span class="html-italic">ZmRALF</span> under different abiotic stresses including drought, heat, salt, and cold. Red and blue boxes indicate high and low expression levels of <span class="html-italic">ZmRALF</span> genes.</p>
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<p>The relative expression patterns of <span class="html-italic">ZmRALF</span> genes under 20% PEG6000 and 200 mM NaCl stresses, as determined by RT-qPCR. (<b>A</b>–<b>C</b>) Expression levels of <span class="html-italic">ZmRALF7</span>, <span class="html-italic">ZmRALF9</span>, and <span class="html-italic">RALF13</span> genes in response to 20% PEG6000 treatment. (<b>D</b>–<b>F</b>) Expression levels of <span class="html-italic">ZmRALF7</span>, <span class="html-italic">ZmRALF9</span>, and <span class="html-italic">RALF13</span> genes in response to 200 mM NaCl treatment. The expression levels at subsequent time points were calculated relative to the 0 h measurement. The data include the standard error (SE) based on three replicates. Different letters indicate significant differences determined by one-way analysis of variance (ANOVA). RT-qPCR analysis utilized the <span class="html-italic">Zm00001d013367</span> gene as an internal control.</p>
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16 pages, 5407 KiB  
Article
Transcriptome and Metabolome Reveal Accumulation of Key Metabolites with Medicinal Properties of Phylloporia pulla
by Ji-Hang Jiang, Qian-Zhu Li, Xing Luo, Jia Yu and Li-Wei Zhou
Int. J. Mol. Sci. 2024, 25(20), 11070; https://doi.org/10.3390/ijms252011070 (registering DOI) - 15 Oct 2024
Viewed by 262
Abstract
Phylloporia pulla, a macrofungal species in the Hymenochaetales, Basidiomycota, is known to enhance the nutritional and bioactive properties of rice through co-fermentation; however, its own secondary metabolites are not well understood. In this study, an integrative analysis of transcriptome and [...] Read more.
Phylloporia pulla, a macrofungal species in the Hymenochaetales, Basidiomycota, is known to enhance the nutritional and bioactive properties of rice through co-fermentation; however, its own secondary metabolites are not well understood. In this study, an integrative analysis of transcriptome and metabolome data revealed that the accumulation of steroids, steroid derivatives, and triterpenoids in P. pulla peaks during the mid-growth stage, while the genes associated with these metabolites show higher expression levels from the early to mid-growth stages. Weighted gene co-expression network analysis identified several modules containing candidate genes involved in the synthesis of steroids, steroid derivatives, and triterpenoids. Specifically, six key hub genes were identified, along with their connectivity to other related genes, as potential catalysts in converting the precursor lanosterol to celastrol. This study enhances our understanding of the secondary metabolites of P. pulla and is essential for the selective utilization of these bioactive compounds. Full article
(This article belongs to the Section Molecular Microbiology)
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<p>Differentially expressed genes (DEGs) of 12 samples at four growth times of liquid fermentation. (<b>A</b>): Principal component analysis of DEGs identified from the 12 samples at four growth times. (<b>B</b>): Heatmap of 4351 DEGs. The abscissa represents the hierarchical clustering of 12 samples at four growth times, and the ordinate represents the hierarchical clustering of DEGs. Red color indicates a high expression level, and purple color indicates a low expression level. (<b>C</b>): Volcano plots showing the down-regulated (Down), up-regulated (Up) and not changed (NoDiff) genes, respectively, indicated with blue, red and grey colors between D1 and another three growth times (D4, D7, and D10). (<b>D</b>): Top 20 enriched KEGG pathways from 4351 differentially expressed genes. The closer the value of false discovery rate (FDR) is to zero, the more significant the enrichment of KEGG pathway is. The circular radius indicates the gene number.</p>
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<p>(<b>A</b>): Expression patterns of DEGs involving the steroids biosynthesis pathway. The abscissa represents the four growth times, and the ordinate represents the hierarchical clustering of DEGs. Orange color represents a high expression level, and blue color corresponds to a low expression level. (<b>B</b>): The steroids biosynthesis pathway with related DEGs and their expression levels at D1, D4, D7 and D10.</p>
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<p>Pearson correlation analysis of DEGs involving the steroids biosynthesis pathways and coding cytochrome P450 monooxygenases with differentially accumulated steroids, steroid derivatives (<b>A</b>), and triterpenoids (<b>B</b>). The abscissa represents the metabolites, and the ordinate represents the DEGs. The blue and red circles represent positive and negative correlations, respectively, and the color represents the value of correlation coefficient. The abs_cor indicates the absolute value of correlation coefficient via the area of circles.</p>
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<p>Diagram of LC-MS/MS analysis of celastrol from mycelia of <span class="html-italic">P. pulla</span> at four growth stages. The selected ion pairs are 451.4/201.0 (<b>A</b>) and 451.4/215.0 (<b>B</b>). STD means the standard substance of celastrol.</p>
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<p>Weighted gene co-expression network analysis. (<b>A</b>): Hierarchical cluster dendrogram showing co-expression modules across four growth times. Each leaf of the dendrogram corresponds to one gene, and the leaves constitute 15 modules, labeled with different colors. (<b>B</b>): Module correlated with steroids and steroid derivatives. (<b>C</b>): Module correlated with triterpenoids. Two triterpenoids, viz. celastrol (M405T116) and lanosterol (M425T108), are indicated in bold font. The numbers in each cell are the correlation coefficient between each gene and metabolite (above) and the corresponding <span class="html-italic">p</span>-value (below). Red color indicates a positive correlation, while green color indicates a negative correlation between the gene and metabolite.</p>
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<p>The co-expression network of genes in the brown module mostly correlated with celastrol. The hub genes are highlighted by red color, and the six key hub genes are indicated by larger circles filled with red color (See <a href="#app1-ijms-25-11070" class="html-app">Table S4</a> for details).</p>
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19 pages, 5544 KiB  
Article
Comprehensive Transcriptomic Analysis Reveals Defense-Related Genes and Pathways of Rice Plants in Response to Fall Armyworm (Spodoptera frugiperda) Infestation
by Xueyan Zhang, Xihao Wang and Tao Wang
Plants 2024, 13(20), 2879; https://doi.org/10.3390/plants13202879 (registering DOI) - 15 Oct 2024
Viewed by 391
Abstract
Rice (Oryza sativa L.) serves as a substitute for bread and is a staple food for half of the world’s population, but it is heavily affected by insect pests. The fall armyworm (Spodoptera frugiperda) is a highly destructive pest, threatening [...] Read more.
Rice (Oryza sativa L.) serves as a substitute for bread and is a staple food for half of the world’s population, but it is heavily affected by insect pests. The fall armyworm (Spodoptera frugiperda) is a highly destructive pest, threatening rice and other crops in tropical regions. Despite its significance, little is known about the molecular mechanisms underlying rice’s response to fall armyworm infestation. In this study, we used transcriptome analysis to explore the global changes in gene expression in rice leaves during a 1 h and 12 h fall armyworm feeding. The results reveal 2695 and 6264 differentially expressed genes (DEGs) at 1 and 12 h post-infestation, respectively. Gene Ontology (GO) and KEGG enrichment analyses provide insights into biological processes and pathways affected by fall armyworm feeding. Key genes associated with hormone regulation, defense metabolic pathways, and antioxidant and detoxification processes were upregulated, suggesting the involvement of jasmonic acid (JA) signaling, salicylic acid biosynthesis pathways, auxin response, and heat shock proteins in defense during 1 h and 12 h after fall armyworm infestation. Similarly, key genes involved in transcriptional regulation and defense mechanisms reveal the activation of calmodulins, transcription factors (TFs), and genes related to secondary metabolite biosynthesis. Additionally, MYB, WRKY, and ethylene-responsive factors (ERFs) are identified as crucial TF families in rice’s defense response. This study provides a comprehensive understanding of the molecular dynamics in rice responding to fall armyworm infestation, offering valuable insights for developing pest-resistant rice varieties and enhancing global food security. The identified genes and pathways provide an extensive array of genomic resources that can be used for further genetic investigation into rice herbivore resistance. This also suggests that rice plants may have evolved strategies against herbivorous insects. It also lays the groundwork for novel pest-resistance techniques for rice. Full article
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<p>Showing the layout of experimental design: (<b>A</b>) infestation of rice plants with FAW larvae for 1 h and 12 h and control; (<b>B</b>) larvae were collected from infested host plants for RNA extraction and cDNA synthesis; (<b>C</b>) high-throughput sequencing and raw data; (<b>D</b>) biological insights; and (<b>E</b>) RTq-PCR analysis for the verification of DEGs data obtained from transcriptome analysis.</p>
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<p>Bar graph showing a total number of up- and downregulated differentially expressed genes (DEGs) in transcriptome analysis of Rice-1h vs. control and Rice-12h vs. control after FAW larvae infestation.</p>
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<p>Gene Ontology (GO) classification of transcripts. The number of significantly up- and downregulated unigenes in Rice-1h vs. control (<b>A</b>) and Rice-12h vs. control (<b>B</b>) after FAW larvae infestation.</p>
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<p>Gene Ontology (GO)-enriched terms of differentially expressed genes (DEGs) and unigenes in Rice-1h vs. control (<b>A</b>) and Rice-12h vs. control (<b>B</b>) after FAW larvae infestation. The <span class="html-italic">x</span>-axis lists the sub-GO terms under categories of biological process, cellular component, and molecular function. The <span class="html-italic">y</span>-axis is the number of DEGs involved in each term.</p>
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<p>Kyoto Encyclopedia of Genes and Genomes (KEGG) annotation and pathways of in Rice-1h vs. control (<b>A</b>) and Rice-12h vs. control (<b>B</b>) after FAW larvae infestation.</p>
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<p>The expression patterns of defensive–responsive genes in in Rice-1h vs. control (<b>A</b>) and Rice-12h vs. control (<b>B</b>) after FAW larvae infestation. Hierarchical clustering heat map depicting overall results of the FPKM clustering using log2 (FPKM + 1) values. The red and blue squares indicate genes with high or low gene expression levels, respectively.</p>
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<p>A number of upregulated genes related to secondary metabolism (<b>A</b>) and transcriptional regulation in Rice-1h vs. control (<b>A</b>) and Rice-12h vs. control (<b>B</b>) after FAW larvae infestation.</p>
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<p>A number of upregulated genes related to hormone regulation (<b>A</b>) and antioxidant and detoxification processes in Rice-1h vs. control (<b>A</b>) and Rice-12h vs. control (<b>B</b>) after FAW larvae infestation.</p>
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<p>(<b>A</b>–<b>F</b>). Results for the qRT-PCR confirmation of the DEGs library. qRT-PCR analysis of ten upregulated genes of detoxification genes: transcriptional regulation (<b>A</b>–<b>F</b>) and hormone regulation (<b>G</b>–<b>L</b>) in Rice-1h vs. control and Rice-12h vs. control after FAW larvae infestation. Different letters a and b indicate significant differences.</p>
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<p>(<b>A</b>–<b>H</b>) Results for the qRT-PCR confirmation of the DEGs library and qRT-PCR analysis of upregulated genes of antioxidants and detoxification genes: Hormone regulation (<b>A</b>–<b>D</b>). Antioxidant and detoxification processes (<b>E</b>–<b>H</b>) in Rice-1h vs. control and Rice-12h vs. control after FAW larvae infestation.</p>
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<p>A working model diagram of molecular insights into the rice plant defense mechanism in response to an insect-attacked plant. Insect-derived elicitors are perceived by unidentified receptors on the plasma membranes, triggering rapid activation of MAPKs followed by biosynthesis of phytohormones, JA, JA-Ile, and ethylene. After several steps of signaling transduction, transcription factors (MYC2 and ERFs, for instance) regulate the accumulation of non-volatile secondary metabolites (such as TPIs in rice), which function as direct defenses against herbivores.</p>
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