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Search Results (10,049)

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11 pages, 1819 KiB  
Article
Cytoplasm of the Wild Species Aegilops mutica Reduces VRN1 Gene Expression in Early Growth of Cultivated Wheat: Prospects for Using Alloplasmic Lines to Breed Varieties Adapted to Global Warming
by Mina Matsumura, Yuko Watanabe, Hiroko Tada and Koji Murai
Plants 2024, 13(23), 3346; https://doi.org/10.3390/plants13233346 (registering DOI) - 28 Nov 2024
Abstract
In a warm winter due to climate warming, it is necessary to suppress early flowering of autumn-sown wheat plants. Here, we propose the use of cytoplasmic genome effects for this purpose. Alloplasmic lines, or cytoplasmic substitution lines, of bread wheat (Triticum aestivum [...] Read more.
In a warm winter due to climate warming, it is necessary to suppress early flowering of autumn-sown wheat plants. Here, we propose the use of cytoplasmic genome effects for this purpose. Alloplasmic lines, or cytoplasmic substitution lines, of bread wheat (Triticum aestivum) have cytoplasm from a related wild Aegilops species through recurrent backcrossing and exhibit altered characteristics compared with the euplasmic lines from which they are derived. Thus, alloplasmic lines with Aegilops mutica cytoplasm show delayed flowering compared with lines carrying normal cytoplasm. In the wheat flowering pathway, VERNALIZATION 1 (VRN1) encodes an APETALA1/FRUITFULL-like MADS box transcription factor that plays a central role in the activation of florigen genes, which induce floral meristems in the shoot apex. Here, we compared expression of VRN1 alleles in alloplasmic and euplasmic lines after vernalization. We found that alloplasmic wheat showed a lower level of VRN1 expression after vernalization compared with euplasmic wheat. Thus, nuclear-cytoplasm interactions affect the expression levels of the nuclear VRN1 gene; these interactions might occur through the pathway termed retrograde signaling. In warm winters, autumn-sown wheat cultivars with spring habit can pass through the reproductive growth phase in very early spring, resulting in a decreased tiller/ear number and reduced yield performance. Here, we present data showing that an alloplasmic line of ‘Fukusayaka’ can avoid the decrease in tiller/ear numbers during warm winters, suggesting that this alloplasmic line may be useful for development of varieties adapted to global warming. Full article
(This article belongs to the Special Issue Wheat Breeding for Global Climate Change)
17 pages, 1598 KiB  
Article
Unraveling Quinoa (Chenopodium quinoa Willd.) Defense Against Downy Mildew (Peronospora variabilis): Comparative Molecular Analysis of Resistant “Hualhuas” and Susceptible “Real” Cultivars
by Walaa Khalifa, Hala Badr Khalil and Marian Thabet
Plants 2024, 13(23), 3344; https://doi.org/10.3390/plants13233344 - 28 Nov 2024
Abstract
Quinoa (Chenopodium quinoa Willd.) is a new, promising non-conventional useful crop; however, its susceptibility to downy mildew, caused by Peronospora variabilis, is a key obstacle limiting its productivity in Egypt. Identifying and utilizing resistant quinoa cultivars appear to be reliable and [...] Read more.
Quinoa (Chenopodium quinoa Willd.) is a new, promising non-conventional useful crop; however, its susceptibility to downy mildew, caused by Peronospora variabilis, is a key obstacle limiting its productivity in Egypt. Identifying and utilizing resistant quinoa cultivars appear to be reliable and cost-efficient strategies for controlling downy mildew, particularly in resource-limited farmers’ fields. This study aimed to evaluate the differential resistance of the Peruvian “Hualhuas” and Bolivian “Real” quinoa cultivars to P. variabilis infection under laboratory conditions to provide precise insight into their basic defense mechanism(s). Inoculated “Hualhuas” plants displayed complete resistance against P. variabilis, with no visible symptoms (incompatible reaction), while those of “Real” plants revealed high susceptibility (compatible reaction), with typical downy mildew lesions on their leaf surfaces. Disease incidence reached about 66% in the inoculated “Real” plants, with most inoculated leaves having lesions of grades 4 and 5 covering up to 90% of their leaf surfaces. Susceptibility indices reached up to 66% in the inoculated “Real” plants. Resistance to P. variabilis observed in the “Hualhuas” plants may have been largely attributed to elevated endogenous H2O2 levels, increased peroxidase (POX) activity and abundance, enhanced phenylalanine ammonia-lyase (PAL) activity and expression, as well as the upregulation of the pathogen-related protein 10 gene (PR-10). The results of this study indicate that the quinoa cultivar “Hualhuas” not only is a promising candidate for sustainable control of quinoa downy mildew but also, through a deep understanding of its molecular resistance mechanisms, would provide a possible route to enhance downy mildew resistance in other genotypes. Full article
19 pages, 1705 KiB  
Article
Spectral Estimation of Chlorophyll for Non-Invasive Assessment in Apple Orchards
by Andrea Szabó, János Tamás and Attila Nagy
Horticulturae 2024, 10(12), 1266; https://doi.org/10.3390/horticulturae10121266 - 28 Nov 2024
Abstract
The main aim of our research was to develop a methodology of chlorophyll content in the leaves of apple trees non-invasive assessment in apple orchards and its adaptation to Early Gold and Golden Reinders based on spectral characteristics of chlorophyll content in the [...] Read more.
The main aim of our research was to develop a methodology of chlorophyll content in the leaves of apple trees non-invasive assessment in apple orchards and its adaptation to Early Gold and Golden Reinders based on spectral characteristics of chlorophyll content in the canopy. In each measurement period, 30 samples were collected from each of the two apple cultivars studied. For spectral data collection of leaf samples, an AvaSpec 2048 spectrometer was used in the wavelength range 400–1000 nm in three replicates. Principal component analysis (PCA) with varimax rotation was used to identify the wavelength with the highest factor weight to identify the chlorophyll-sensitive wavelength. The models were calibrated with 2/3 of the values in the database and validated with the remaining 1/3. The simple linear regression method generated the model for estimating chlorophyll. The coefficient of determination (R2) was used to compare the strength of the regression models, and the Root Mean Square Error (RMSE), Normalized Root Mean Square Error (NRMSE), Nash–Sutcliffe efficiency (NSE), Mean Absolute Error (MAE) and Mean Bias Error (MBE) functions were used to measure the accuracy of the estimator models. These metrics help to quickly assess how reliable and accurate a model’s predictions are. Nine indices were obtained based on the precision values, and CHLapple1 performed best (R2 = 0.633, RMSE = 298.28 µg/g, NRMSE = 9.61%, NSE = 0.60 MBE = 84.59, and MAE = 243.39). Full article
(This article belongs to the Section Biotic and Abiotic Stress)
15 pages, 2445 KiB  
Article
Physiology and Metabolism Alterations in Flavonoid Accumulation During Buckwheat (Fagopyrum esculentum Moench.) Sprouting
by Meixia Hu, Jia Yang, Jing Zhang, Weiming Fang and Yongqi Yin
Plants 2024, 13(23), 3342; https://doi.org/10.3390/plants13233342 - 28 Nov 2024
Abstract
In this research, we investigated the physiological modifications, flavonoid metabolism, and antioxidant systems of two buckwheat (Fagopyrum esculentum Moench.) cultivars, Pintian and Suqiao, during germination. The results demonstrated an initial increase followed by a subsequent decline in the flavonoid content of the [...] Read more.
In this research, we investigated the physiological modifications, flavonoid metabolism, and antioxidant systems of two buckwheat (Fagopyrum esculentum Moench.) cultivars, Pintian and Suqiao, during germination. The results demonstrated an initial increase followed by a subsequent decline in the flavonoid content of the buckwheat sprouts throughout germination. On the third day of germination, the highest flavonoid concentrations were observed, with the Pintian and Suqiao varieties reaching 996.75 and 833.98 μg/g fresh weight, respectively. Both the activity and relative gene expression level of the flavonoid metabolizing enzyme showed a significant rise in 3-day-old buckwheat sprouts, which was strongly correlated with the flavonoid content. The correlation analysis revealed that the buckwheat sprouts accumulated flavonoids by enhancing the activities and gene expression levels of flavonoid synthases. The antioxidant capacity and the activities and gene expression profiles of the antioxidant enzymes in both buckwheat cultivars notably increased after three days of germination. The correlation analysis indicated a significant positive link between antioxidant capacity and the activity and gene expression levels of the antioxidant enzymes, flavonoid content, and total phenol content. This research demonstrated that germination treatment can significantly boost the accumulation of flavonoids and total phenols, thereby enhancing the antioxidant properties of buckwheat sprouts, despite variations among different buckwheat varieties. Full article
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Figure 1

Figure 1
<p>Changes in growth morphology (<b>I</b>), fresh weight (<b>II</b>), total phenolic content (<b>III</b>), and flavonoid content (<b>IV</b>) in buckwheat sprouts. Distinct lowercase letters signify statistically significant differences in germination times for the same buckwheat cultivar (<span class="html-italic">p</span> &lt; 0.05). Asterisks (*) denote significant differences among buckwheat cultivars at identical germination times (<span class="html-italic">p</span> &lt; 0.05). PT: Pintian. SQ: Suqiao.</p>
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<p>Changes in the capacities of DPPH (<b>I</b>), ABTS (<b>II</b>), and FRAP (<b>III</b>) in buckwheat sprouts are shown. Distinct lowercase letters signify statistically significant differences in germination times for the same buckwheat cultivar (<span class="html-italic">p</span> &lt; 0.05). Asterisks (*) denote significant differences among buckwheat cultivars at identical germination times (<span class="html-italic">p</span> &lt; 0.05). PT: Pintian. SQ: Suqiao.</p>
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<p>Changes in the activities of PAL (<b>I</b>), C4H (<b>II</b>), 4CL (<b>III</b>), and CHI (<b>IV</b>) and the expression levels of <span class="html-italic">PAL</span> (<b>V</b>), <span class="html-italic">C4H</span> (<b>VI</b>), <span class="html-italic">4CL</span> (<b>VII</b>), <span class="html-italic">CHI</span> (<b>VIII</b>), <span class="html-italic">CHS</span> (<b>IX</b>), and <span class="html-italic">F3H</span> (<b>X</b>) in buckwheat sprouts. Distinct lowercase letters signify statistically significant differences in germination times for the same buckwheat cultivar (<span class="html-italic">p</span> &lt; 0.05). Asterisks (*) denote significant differences among buckwheat cultivars at identical germination times (<span class="html-italic">p</span> &lt; 0.05). PT: Pintian. SQ: Suqiao.</p>
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<p>Changes in the activity of POD (<b>I</b>), CAT (<b>II</b>), SOD (<b>III</b>), and APX (<b>IV</b>) and the expression levels of <span class="html-italic">POD</span> (<b>V</b>), <span class="html-italic">CAT</span> (<b>VI</b>), <span class="html-italic">SOD</span> (<b>VII</b>), and <span class="html-italic">APX</span> (<b>VIII</b>) in buckwheat sprouts. Distinct lowercase letters signify statistically significant differences in germination times for the same buckwheat cultivar (<span class="html-italic">p</span> &lt; 0.05). Asterisks (*) denote significant differences among buckwheat cultivars at identical germination times (<span class="html-italic">p</span> &lt; 0.05). PT: Pintian. SQ: Suqiao.</p>
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<p>The examination of the correlation analysis of flavonoids with various indexes in Pintian sprouts and Suqiao sprouts is represented by (<b>I</b>) and (<b>II</b>), respectively. Negative correlations are indicated by shades of purple, blue, and green, whereas positive correlations are represented by shades of red. The correlation coefficients can vary from −1 to 1. Asterisks (*) and (**) denote that the correlation coefficient is statistically significant at <span class="html-italic">p</span>-value thresholds of 0.05 and 0.01, respectively. PT: Pintian; SQ: Suqiao.</p>
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<p>The mechanism diagram of germination that regulates the antioxidant system and the flavonoid metabolism system of buckwheat sprouts.</p>
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17 pages, 4704 KiB  
Article
Physiological Mechanism of EBR for Grain-Filling and Yield Formation of Tartary Buckwheat
by Han Liu, Qiang Wang, Ting Cheng, Yan Wan, Wei Wei, Xueling Ye, Changying Liu, Wenjun Sun, Yu Fan, Liang Zou, Laichun Guo and Dabing Xiang
Plants 2024, 13(23), 3336; https://doi.org/10.3390/plants13233336 - 28 Nov 2024
Abstract
Tartary buckwheat is characterized by its numerous inflorescences; however, the uneven distribution of resources can lead to an overload in certain areas, significantly limiting plant productivity. Plant growth regulators effectively modulate plant growth and development. This study investigated the effects of three concentrations [...] Read more.
Tartary buckwheat is characterized by its numerous inflorescences; however, the uneven distribution of resources can lead to an overload in certain areas, significantly limiting plant productivity. Plant growth regulators effectively modulate plant growth and development. This study investigated the effects of three concentrations of brassinosteroids (EBR) on the Tartary buckwheat cultivar with high seed-setting rates, specifically Chuanqiao No. 1 (CQ1), and low seed-setting rates, namely Xiqiao No. 1 (XQ1), through field experiments. The goal was to investigate how EBR regulates buckwheat grain-filling, enhancing the seed-setting rates, and to understand the physiological mechanisms behind this improvement. The results indicated that EBR treatment followed the typical “S” type growth curve of crops, resulting in an increase in the Tartary buckwheat grain-filling rate. Varieties with high seed-setting rates demonstrated a greater capacity for grain-filling. EBR was observed to regulate hormone content, enhance the photosynthetic capacity of Tartary buckwheat, and increase yield. This was accomplished by enhancing the accumulation of photosynthetic products during the grain-filling period. Specifically, EBR elevated the activity of several key enzymes, including pre-leaf sucrose phosphate synthase (SPS), seed sucrose synthase (SS), late grain-filling acid invertase (AI), grain-filling leaf SPS, and grain SS. These changes led to an increased accumulation of sucrose and starch from photosynthetic products. In summary, the G2 concentration of EBR (0.1 mg/L) demonstrated the most significant impact on the seed-setting rates and yield enhancement of Tartary buckwheat. Full article
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Figure 1

Figure 1
<p>The agronomic traits (<b>A</b>–<b>G</b>) and seed-setting (<b>H</b>–<b>L</b>) of Tartary buckwheat under various growth regulator treatments. The parameters assessed include plant height (<b>A</b>), the number of main stem branches (<b>B</b>), the number of central stem nodes (<b>C</b>), the number of grains per plant (<b>D</b>), thousand-grain weight (<b>E</b>), yield (<b>G</b>), the total number of flowers (<b>H</b>), the number of dead flowers (<b>I</b>), the number of dead grains (<b>J</b>), the number of mature grains (<b>K</b>), and the seed-setting rate (<b>L</b>). Values in the graph reflect means; error bars show SEM. Different letters denote significant differences among means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The agronomic traits (<b>A</b>–<b>I</b>), plant height (<b>A</b>), number of branches of main stem bran (<b>B</b>), number of nodes in main stem (<b>C</b>), grain number per plant (<b>D</b>), grain weight per plant (<b>E</b>), 1000-grain weight (<b>F</b>), yield (<b>G</b>), actual grain-leaf ratio (<b>H</b>), total grain-leaf ratio (<b>I</b>). as well as the fruiting conditions of CQ1 (<b>J</b>) and XQ1 (<b>K</b>), under varying concentrations of EBR treatments. CQ1 refers to Sichuan Buckwheat No. 1, while XQ1 denotes Xiqiao No. 1. G0, G1, G2, and G3 represent the four concentrations of EBR, i.e., 0 mg/L, 0.05 mg/L, 0.1 mg/L, and 0.2 mg/L. Values in the graph show the means; error bars show SEM. Different letters denote significant differences among means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The chlorophyll content (AI) on various days under different EBR concentration treatments. The figure includes CQ1 chlorophyll a content (<b>A</b>), chlorophyll b content (<b>B</b>), and total chlorophyll content (<b>C</b>), as well as XQ1 chlorophyll a content (<b>D</b>), chlorophyll b content (<b>E</b>), and total chlorophyll content (<b>F</b>). Values in the graph reflect means; error bars indicate SEM. Different letters denote significant differences among means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The enzyme content related to carbon metabolism (AL) under varying concentrations of EBR treatments. The accumulation of flowers, stems, and leaves are presented over three time points: 10 days (<b>A</b>), 20 days (<b>B</b>), and 30 days (<b>C</b>). Additionally, the grain sucrose content is shown for CQ1 (<b>D</b>) and XQ1 (<b>E</b>), followed by the grain starch content for CQ1 (<b>F</b>) and XQ1 (<b>G</b>). The figure further details sucrose synthase activity for CQ1 (<b>H</b>) and XQ1 (<b>I</b>), acid invertase activity for CQ1 (<b>J</b>) and XQ1 (<b>K</b>), and sucrose phosphate synthase activity for CQ1 (<b>L</b>) and XQ1 (<b>M</b>). Finally, the sucrose content in the leaves is represented for CQ1 (<b>N</b>) and XQ1 (<b>O</b>). CQ1 denotes Chuanqiao Buckwheat No. 1, while XQ1 refers to Xiqiao No. 1. Values in the graph reflect means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Chlorophyll concentration (<b>A</b>–<b>D</b>) on different days under different EBR concentration treatments. Indole-3-acetic acid (IAA) content (<b>A</b>); abscisic acid (ABA) content (<b>B</b>); zeatin (TZ) content (<b>C</b>); gibberellin (GA<sub>3</sub>) content (<b>D</b>). CQ1 stands for Chuanqiao No. 1; XQ1 stands for Xiqiao No. 1. Values in the graph reflect means; error bars indicate SEM. Different letters denote significant differences among means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Biplot of CQ- and XQ1-related traits under different EBR concentration treatments. The indicators include Chla (chlorophyll a), Chlb (chlorophyll b), TChl (total chlorophyll), A (net photosynthetic rate), Gs (stomatal conductance), WUE (transpiration rate), Ci (intercellular CO<sub>2</sub> concentration), SS (sucrose synthase), AI (acid invertase), starch (starch), SPS (sucrose phosphate synthase), sucrose-seed (grain sucrose), and sucrose-leaf (leaf sucrose).</p>
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<p>Mechanism diagram of EBR regulating yield increase of Tartary buckwheat. The red arrows indicate an increase, while the blue arrows indicate a decrease.</p>
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<p>Chengdu weather conditions in 2018 (<b>A</b>) and 2019 (<b>B</b>). The data comes from the website <a href="http://www.worldweatheronline.com" target="_blank">www.worldweatheronline.com</a>.</p>
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17 pages, 3661 KiB  
Article
Investigating the Rhizosphere Fungal Communities of Healthy and Root-Rot-Infected Lycium barbarum in the Tsaidam Basin, China
by Guozhen Duan, Guanghui Fan, Jianling Li, Min Liu and Youchao Qi
Microorganisms 2024, 12(12), 2447; https://doi.org/10.3390/microorganisms12122447 - 28 Nov 2024
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Abstract
Lycium barbarum is a plant of considerable economic importance in China. However, root rot poses a significant threat to its yield and quality, leading to substantial economic losses. The disparities in rhizosphere soil fungal communities between healthy and root-rot-affected L. barbarum have not [...] Read more.
Lycium barbarum is a plant of considerable economic importance in China. However, root rot poses a significant threat to its yield and quality, leading to substantial economic losses. The disparities in rhizosphere soil fungal communities between healthy and root-rot-affected L. barbarum have not been thoroughly explored. Delving into the dynamics between these fungal communities and the onset of root rot may provide pivotal insights for the biological control of this disease in L. barbarum, as well as aid in identifying fungi associated with the condition. In this study, we utilized rhizosphere soil samples from Ningqi No. 1, a distinguished cultivar of L. barbarum, as our experimental material. We assessed the composition and diversity of fungal communities in both diseased (D) and healthy (H) samples using Illumina MiSeq sequencing technology. The study’s findings revealed that the mean concentrations of total nitrogen (TN) and soil organic matter (SOM) were significantly higher in the healthy specimens when contrasted with the diseased ones, while the pH levels were notably increased in the latter group. Additionally, the alpha-diversity of fungal communities was observed to be greater within the healthy samples as opposed to the diseased samples. Marked distinctions in fungal diversity were discerned between the healthy (H) and diseased (D) samples. Ascomycota was identified as the predominant fungal phylum in both groups. In the healthy samples, beneficial fungi such as Plectosphaerella and Mortierella were prevalent, in contrast to the diseased samples, the relative abundances of Embellisia and Alternaria demonstrated remarkable increases of 89.59% and 87.41%, respectively. Non-metric Multidimensional Scaling (NMDS) illustrated clear distinctions in the composition of fungal communities between the healthy and diseased samples. Redundancy Analysis (RDA) indicated total nitrogen (TN), organic matter (SOM), total phosphorus (TP), Available Potassium (AK), pH, and Total Potassium (TK). Notably, pH showed a stronger correlation with the diseased samples, while TN and SOM were more significantly associated with the healthy samples. Full article
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Figure 1

Figure 1
<p>(<b>A</b>) represents the sampling sites of <span class="html-italic">L. barbarum</span>; (<b>B</b>) depicts leaves exhibiting wilted conditions; (<b>C</b>) illustrates the stems in contact with the ground, which have been excavated to inspect for swelling; (<b>D</b>) contrasts the root systems of healthy plants (H) with those of infected plants (D); (<b>E</b>) shows the post-fruiting performance of the infected plants; and (<b>F</b>) displays the outcomes of the healthy plants.</p>
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<p>The analysis of soil physicochemical properties, where (<b>A</b>) is total nitrogen (TN), (<b>B</b>) is total potassium (TK), (<b>C</b>) is total phosphorus (TP), (<b>D</b>) is soil organic matter (SOM), (<b>E</b>) is alkali-hydrolyzable nitrogen (AN), (<b>F</b>) is available phosphorus (AP), (<b>G</b>) is available potassium (AK), and (<b>H</b>) is pH values. Letters indicate significant differences among different soil samples by ANOVA at <span class="html-italic">p</span> * &lt; 0.05, <span class="html-italic">p</span> ** &lt; 0.01 vs. H group (n = 17 in each group). H is healthy samples; D is diseased samples.</p>
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<p>(<b>A</b>) The OTU distribution Venn diagram; (<b>B</b>) The saturation of rarefaction curves; (<b>C</b>) The Observed Operational Taxonomic Units (OTUs); (<b>D</b>) The Chao1 richness index; (<b>E</b>) Simpson’s diversity index; (<b>F</b>) The Shannon-Wiener diversity index. Utilizing Illumina sequencing technology, Venn diagram is at a 97% sequence similarity threshold, and the OTU distribution Venn diagram shows that the D group harbored 830 unique OTUs, accounting for 32.07% of the total, while the H group had 1112 unique OTUs, comprising 42.97% of the total. Only 646 OTUs were shared between the two groups, representing 24.96% of the total. These data clearly indicate a higher fungal richness in the H group compared to the D group. The rarity curve saturation in (<b>B</b>) suggests that the sequencing depth was sufficient to capture the full spectrum of fungal community diversity in the rhizospheric soil. Consequently, these findings are deemed to accurately represent the actual state of the fungal communities and are suitable for further analysis. (<b>C</b>–<b>F</b>) illustrate the alpha diversity of the soil fungal communities within each sample, evaluated by multiple metrics, including the number of observed OTUs, the Chao1 richness index, the Simpson diversity index, and the Shannon-Wiener diversity index. Notably, significant differences were found between the D and H groups for all indices, with the H soils exhibiting a higher level of diversity than the D soils. * indicate significant differences among different soil samples by ANOVA at <span class="html-italic">p</span> &lt; 0.05, ** indicate significant differences among different soil samples by ANOVA at <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>(<b>A</b>,<b>B</b>): Variation in microbial abundance at the phylum and genus levels; (<b>C</b>,<b>D</b>): H and D microbes with differential abundance at the phylum and genus levels. (<b>A</b>–<b>D</b>) collectively illustrate the composition and relative abundance of the fungal community in the rhizospheric soil of wolfberry. (<b>A</b>) reveals the distribution of over nine distinct fungal phyla, with Ascomycota being the predominant group, averaging a 74.78% abundance, followed by Zygomycota, Basidiomycota, and Chytridiomycota. (<b>C</b>) discloses significant differences in the fungal communities between healthy (H) and root-rot (D) samples, where the abundance of Ascomycota increased by 10.43% in the D samples, while the abundance of Basidiomycota and Glomeromycota significantly decreased. (<b>B</b>,<b>D</b>) further analyze the distribution of fungal genera, with 332 genera exhibiting significant changes under different treatments; a higher abundance of <span class="html-italic">Plectosphaerella</span>, <span class="html-italic">Mortierella</span>, <span class="html-italic">Kotlabaea</span>, and <span class="html-italic">Neonectria</span> was observed in healthy samples, whereas the abundance of <span class="html-italic">Embellisia</span> and <span class="html-italic">Alternaria</span> significantly increased in D samples. These findings indicate that root rot significantly alters the structure of the fungal community in the rhizospheric soil, exerting a substantial impact on agricultural production. ** indicate significant differences among different soil samples by ANOVA at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Relative abundances of fungal classes in rhizosphere soil samples. NMDS analysis (<b>A</b>), coupled with LEfSe analysis (<b>B</b>), has elucidated significant distinctions in the fungal communities of the rhizosphere soil between healthy (H) and root-rot infected (D) in <span class="html-italic">L. barbarum</span> plants. The NMDS analysis revealed a notable differentiation in the fungal community structure between the two groups, with a stress value of 0.17, indicating statistically significant results. The fungal communities in the healthy plants exhibited greater consistency, whereas those in the infected plants were more dispersed. The LEfSe analysis further revealed significant differences in the relative abundance and distribution of fungi at the phylum, class, family, and genus levels between the H and D soil samples. Notably, the H samples registered higher LDA scores for Basidiomycota, Glomeromycota, Eurotiomycetes, Sordariomycetes, Chytridiomycetes, and Glomeromycetes, whereas the D samples were enriched with Dothideomycetes, Cucurbitariaceae, and Pleosporaceae. At the genus level, the H samples were characterized by the highest LDA scores for <span class="html-italic">Phoma</span>, <span class="html-italic">Bionectria</span>, <span class="html-italic">Neonectria</span>, <span class="html-italic">Plectosphaerella</span>, <span class="html-italic">Verticillium</span>, and <span class="html-italic">Glomus</span>, while the D samples were distinguished by the prominence of <span class="html-italic">Pyrenochaeta</span>, <span class="html-italic">Didymella</span>, <span class="html-italic">Alternaria</span>, <span class="html-italic">Embellisia</span>, and <span class="html-italic">Phaeomycocentrospora</span>.</p>
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<p>RDA of chemical properties and fungal communities in rhizosphere soils. RDA collectively elucidates the influence of soil chemical properties on the fungal community structure in the rhizosphere soil of <span class="html-italic">L. barbarum</span>. The RDA revealed that chemical attributes such as total nitrogen (TN), soil organic matter (SOM), and total phosphorus (TP) significantly affect the relative abundance of fungal genera, with TN emerging as a predominant influencing factor, positively correlating with the microbial communities associated with healthy plants. Conversely, pH exerted a pivotal impact on the distribution of fungi in the rhizosphere of diseased plants.</p>
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<p>The predicted trophic mode and subguilds bar graph by FUNguild (<b>A</b>,<b>B</b>) and Network diagram of fungal taxonomic trophic model interactions by cytoscape (<b>C</b>,<b>D</b>). In (<b>A</b>,<b>B</b>), we have evaluated the functional roles of soil fungi in both healthy and root-rot infected <span class="html-italic">L. barbarum</span> plants, categorizing the fungi into eight trophic modes and sixty-eight subgroups. C and D are Network diagrams drawn according to trophic mode in the H and D groups, where node represents trophic mode classification, node size represents OTU data values, Fn 1, Fn 2, Fn 3, etc. are abbreviations for OTU, blue lines represent two OTU with positive relationships, and red lines represent negative relationships between two OTU, through the analysis conducted via FUNGuild. The study revealed that 80.4% of the nutritional modes were understood in the healthy plants, while 79.9% were predicted in the infected ones. Notably, the pathotrophic (P) and saprotrophic (Sa) nutritional types exhibited significant positive and negative interactions, respectively, in both the healthy (H) and infected (D) plants. Pathogens were more prevalent in the infected plants, whereas the healthy plants predominantly harbored mutualistic and saprotrophic fungi.</p>
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16 pages, 3842 KiB  
Article
Genetic Diversity and Subspecific Races of Upland Cotton (Gossypium hirsutum L.)
by Asiya K. Safiullina, Dilrabo K. Ernazarova, Ozod S. Turaev, Feruza U. Rafieva, Ziraatkhan A. Ernazarova, Sevara K. Arslanova, Abdulqahhor Kh. Toshpulatov, Barno B. Oripova, Mukhlisa K. Kudratova, Kuvandik K. Khalikov, Abdulloh A. Iskandarov, Mukhammad T. Khidirov, John Z. Yu and Fakhriddin N. Kushanov
Genes 2024, 15(12), 1533; https://doi.org/10.3390/genes15121533 - 28 Nov 2024
Viewed by 179
Abstract
Background/Objectives: The classification and phylogenetic relationships of Gossypium hirsutum L. landraces, despite their proximity to southern Mexico, remain unresolved. This study aimed to clarify these relationships using SSR markers and hybridization methods, focusing on subspecies and race differentiation within G. hirsutum L. [...] Read more.
Background/Objectives: The classification and phylogenetic relationships of Gossypium hirsutum L. landraces, despite their proximity to southern Mexico, remain unresolved. This study aimed to clarify these relationships using SSR markers and hybridization methods, focusing on subspecies and race differentiation within G. hirsutum L. Methods: Seventy polymorphic SSR markers (out of 177 tested) were used to analyze 141 alleles and calculate genetic distances among accessions. Phylogenetic relationships were determined using MEGA software (version 11.0.13) and visualized in a phylogenetic tree. ANOVA in NCSS 12 was used for statistical analysis. Over 1000 inter-race crosses were conducted to assess boll-setting rates. Results: Distinct phylogenetic patterns were identified between G. hirsutum subspecies and races, correlating with boll-setting rates. Latifolium, richmondii, and morilli showed no significant increase in boll-setting rates in reciprocal crosses. Cultivars Omad and Bakht, as paternal parents, yielded higher boll-setting rates. Religiosum and yucatanense displayed high boll- and seed-setting rates as maternal parents but low rates as paternal parents. Additionally, phylogenetic analysis revealed a close relationship between cultivars ‘Omad’ and ‘Bakht’ with G. hirsutum race richmondii, indicating their close evolutionary relationship. Conclusions: Reciprocal differentiation characteristics of G. hirsutum subspecies and races, particularly religiosum and yucatanense, should be considered during hybridization for genetic and breeding studies. Understanding the phylogenetic relationships among G. hirsutum taxa is crucial for exploring the genetic diversity of this economically important species. Full article
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<p>The studied subspecies and races of <span class="html-italic">G. hirsutum</span> L. (<b>A</b>) subsp. <span class="html-italic">euhirsutum</span> (Omad cultivar); (<b>B</b>) subsp. <span class="html-italic">euhirsutum</span> (Bakht cultivar); (<b>C</b>) subsp. <span class="html-italic">paniculatum</span>; (<b>D</b>) subsp. <span class="html-italic">mexicanum</span>; (<b>E</b>) subsp. <span class="html-italic">punctatum</span>; (<b>F</b>) race <span class="html-italic">yucatanense</span>.</p>
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<p>The studied subspecies and races of <span class="html-italic">G. hirsutum</span> L. (<b>A</b>) race <span class="html-italic">richmondii</span>; (<b>B</b>) race <span class="html-italic">religiosum</span>; (<b>C</b>) race <span class="html-italic">morilli</span>; (<b>D</b>) race <span class="html-italic">latifolium</span>.</p>
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<p>Boll- and seed-setting rates of the hybrids between <span class="html-italic">G. hirsutum</span> subspecies and races. (<b>A</b>) <span class="html-italic">G. hirsutum × latifolium</span>; (<b>B</b>) <span class="html-italic">G. hirsutum × religiosum</span>; (<b>C</b>) <span class="html-italic">G. hirsutum × richmondii</span>; (<b>D</b>) <span class="html-italic">G. hirsutum × morilli</span>; (<b>E</b>) <span class="html-italic">G. hirsutum × yucatanense</span>.</p>
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<p>PCR-based analysis of cotton genetic polymorphisms using SSR markers. (<b>A</b>) Gh433; (<b>B</b>) NAU1221; (<b>C</b>) NAU1042; (<b>D</b>) NAU2265. M—molecular weight marker (base pairs, bp). (1) subsp. <span class="html-italic">mexicanum</span>; (2) subsp. <span class="html-italic">punctatum</span> (Fanome); (3) subsp. <span class="html-italic">paniculatum</span>; (4) race <span class="html-italic">latifolium</span>; (5) race <span class="html-italic">morilli</span>; (6) race <span class="html-italic">religiosum</span>; (7) race <span class="html-italic">yucatanense</span>; (8) race <span class="html-italic">richmondii</span>; (9) subsp. <span class="html-italic">euhirsutum</span> (cultivar ‘Omad’); (10) subsp. <span class="html-italic">euhirsutum</span> (cultivar ‘Bakht’).</p>
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<p>The phylogenetic tree of studied <span class="html-italic">G. hirsutum</span> accessions. Evolutionary relationships among subspecies and races of upland cotton are illustrated in this phylogenetic tree, which was constructed using the Neighbor-Joining method of the PAUP 4.0 (Phylogenetic Analysis Using Parsimony) program based on genetic distances calculated from 70 polymorphic SSR markers. The numerical values on the branches represent genetic distances, reflecting the degree of divergence between the accessions. A scale bar is included to indicate the proportional relationship between genetic distance values and the extent of evolutionary divergence.</p>
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17 pages, 2628 KiB  
Article
“Low-Hanging Fruit” Practices for Improving Water Productivity of Rainfed Potatoes Using Integration of Cultivar Selection, Mulch Application, and Different Agroecological Zones in Sub-Tropical, Semi-Arid Regions
by Nosipho Precious Minenhle Phungula, Sandile Thamsanqa Hadebe, Elmar Schulte-Geldermann, Lucky Sithole and Nomali Ziphorah Ngobese
Water 2024, 16(23), 3422; https://doi.org/10.3390/w16233422 - 28 Nov 2024
Viewed by 190
Abstract
Unevenly distributed rainfall leads to reduced potato water productivity (WP) under rainfed production conditions. Understanding the practices that can increase WP is vital. Our objectives were to understand (i) the seasonal variables that influence WP under rainfed conditions and (ii) the effect of [...] Read more.
Unevenly distributed rainfall leads to reduced potato water productivity (WP) under rainfed production conditions. Understanding the practices that can increase WP is vital. Our objectives were to understand (i) the seasonal variables that influence WP under rainfed conditions and (ii) the effect of the integration of cultivar x locality x mulch on potato WP. The study was undertaken in smallholder settings in two agroecological zones: Appelsbosch (Mbalenhle locality) and Swayimane (Stezi and Mbhava locality). A split plot, in a randomized complete block design experiment, included mulching (mulch and no mulch), four selected cultivars, and s three localities. Soil water content (SWC), yield, and climatic data were collected, and actual crop evapotranspiration (ETa) and WP were calculated. Rainfall, ETa, and crop growth and development had a significant influence on the seasonal WP. Cultivar × mulch × locality had an insignificant effect on the WP, however, locality × cultivar significantly altered the WP. The localities that had lower vapor pressure deficit (VPD), high relative humidity, and sandy soil had a higher potato WP for all cultivars, with the highest (18.38 kg m−3) being that from Electra. The findings suggest that using localities that have less atmospheric dryness and a cultivar (Electra) that shows stability of yield across the seasons can be an easy-to-apply practice for increasing potato WP in a resource-limited environment. Full article
(This article belongs to the Section Water, Agriculture and Aquaculture)
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<p>The study area shows three localities (Stezi, Mbhava, and Mbalenhle).</p>
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<p>Weather data [rainfall, relative humidity (RH), reference evapotranspiration (ETo), and air temperature] distribution according to growth stages [initial stage (IS), development stage (DS), mid-season stage (MS), and late-season stage (LS)] of the two growing seasons (2022/23 and 2023/24), for Mbalenhle, Mbhava, and Stezi.</p>
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<p>Seasonal measured variables: water productivity (<b>A</b>), yield (<b>B</b>), crop actual evapotranspiration, ETa (<b>C</b>), rainfall (<b>D</b>), maximum canopy cover, CCx (<b>E</b>), and duration of maximum canopy cover (<b>F</b>). Error bars is the standard deviation, bars with the same letter differ non-significantly (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Seasonal rainfall distribution according to growth stages for season 1 (2022/23) and season 2 (2023/24).</p>
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<p>Localities’ seasonal rainfall, drainage, actual crop evapotranspiration (ETa), and changes in soil water content (SWC) for 2022/23 and 2023/2.</p>
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<p>Soil water content (SWC) and rainfall for Mbalenhle, Mbhava, and Stezi for the 2022/23 and 2023/24 seasons. Field capacity (FC), permanent wilting point (PWP), and saturation (SAT).</p>
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<p>Maximum canopy cover (CCx) of selected cultivars across localities [(<b>A</b>) 2022/23 and (<b>B</b>) 2023/24] and duration of CCx [(<b>C</b>) 2022/23 and (<b>D</b>) 2023/24]. Error bars is the standard deviation, bars with the same letter differ non-significantly (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Maximum canopy cover (CCx) of selected cultivars across localities [(<b>A</b>) 2022/23 and (<b>B</b>) 2023/24] and duration of CCx [(<b>C</b>) 2022/23 and (<b>D</b>) 2023/24]. Error bars is the standard deviation, bars with the same letter differ non-significantly (<span class="html-italic">p</span> &gt; 0.05).</p>
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15 pages, 2664 KiB  
Article
Analysis on Unveiling the Natural Dynamics of Parthenocarpy and Self-Compatibility in Apple Trees
by Rongmei Wu, Xiaoying Chen, Bin Xia, Yujia Yang, Claire Molloy, Ruiling Wang, Hilary S. Ireland, Robert J. Schaffer, Satish Kumar and Jia-Long Yao
Horticulturae 2024, 10(12), 1261; https://doi.org/10.3390/horticulturae10121261 - 28 Nov 2024
Viewed by 190
Abstract
Apple (Malus domestica) is self-incompatible and typically requires cross-pollination for seed and fruit development. Parthenocarpy (fruit development without fertilization) and self-compatibility (fruit set without external pollen) are highly desirable traits in apple breeding, as they ensure consistent fruit production and quality [...] Read more.
Apple (Malus domestica) is self-incompatible and typically requires cross-pollination for seed and fruit development. Parthenocarpy (fruit development without fertilization) and self-compatibility (fruit set without external pollen) are highly desirable traits in apple breeding, as they ensure consistent fruit production and quality without cross-pollination. However, apple parthenocarpic and self-compatible accessions have not been available for practical breeding. To identify these accessions, we analysed 436 accessions of Malus domestica and 84 accessions of wild Malus species by assessing fruit production. Flowers were bagged before opening to prevent cross-pollination. If fruit developed from the bagged flowers, it indicated the presence of self-compatibility or parthenocarpy, depending on whether the fruit contained seeds. We observed and scored a range of phenotypic expressions among accessions, from weak to strong in both parthenocarpy and potential self-compatibility. Strong parthenocarpy was observed in 5.95% of wild Malus species accessions and 3.44% of M. domestica accessions. Similarly, strong self-compatibility was exhibited in 5.95% of wild Malus species accessions and 2.75% of M. domestica accessions. Although bagged flowers showed lower fruit set rates than open-pollinated (OP) flowers, fruit size, weight, firmness, and soluble sugar and starch content showed no significant differences between fruits produced from bagged and OP flowers. Furthermore, a genome-wide association study (GWAS) was conducted with a high-throughput SNP array. This analysis identified several genes potentially associated with these traits. This research provides parthenocarpic and self-compatible apple accessions for breeding, which can generate novel cultivars that eliminate the need for cross-pollination or produce seedless fruit without pollination. Full article
(This article belongs to the Special Issue Research on Germplasm Resources and Genetic Improvement of Tree Fruit)
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<p>(<b>A</b>) Representative picture of bagged flower and naturally pollinated (OP) flower on a tree. (<b>B</b>) Double-bagged flowers, with an inner paper bag and outer net bag.</p>
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<p>Phenotypic analysis of fruit derived from open-pollinated (OP) and bagged flowers of <span class="html-italic">Malus domestica</span> accessions. (<b>A</b>) Parthenocarpic accessions ‘CJ07’, ‘MM114’, ‘Prince Alfred’, and ‘Double Red Wealthy’. Seeds were found in the fruit derived from OP flowers (bottom panel) but not found in fruit derived from bagged flowers (upper panel). (<b>B</b>) The graph shows the average fruit weight of those derived from OP and bagged flowers of 22 parthenocarpic accessions. (<b>C</b>) Photographs show whole and cut fruit of five self-compatible accessions ‘Katja’, ‘Krugers Dickstiel’, ‘MM105’, ‘Rome Beauty’, and ‘Yoko’. Seeds were found in the fruit derived from both OP (bottom panel) and bagged flowers (upper panel). (<b>D</b>) The graph shows average fruit weight of those derived from OP and bagged flowers of 26 self-compatible accessions. The error bars present SE of three fruits for OP accessions, and variable fruits for bagged accessions. Asterisks indicate significant differences between bagged and OP fruits (*, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01, Student’s test).</p>
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<p>Phenotypic analysis of fruit derived from open-pollinated (OP) and bagged flowers of <span class="html-italic">Malus domestica</span> accessions. (<b>A</b>) Parthenocarpic accessions ‘CJ07’, ‘MM114’, ‘Prince Alfred’, and ‘Double Red Wealthy’. Seeds were found in the fruit derived from OP flowers (bottom panel) but not found in fruit derived from bagged flowers (upper panel). (<b>B</b>) The graph shows the average fruit weight of those derived from OP and bagged flowers of 22 parthenocarpic accessions. (<b>C</b>) Photographs show whole and cut fruit of five self-compatible accessions ‘Katja’, ‘Krugers Dickstiel’, ‘MM105’, ‘Rome Beauty’, and ‘Yoko’. Seeds were found in the fruit derived from both OP (bottom panel) and bagged flowers (upper panel). (<b>D</b>) The graph shows average fruit weight of those derived from OP and bagged flowers of 26 self-compatible accessions. The error bars present SE of three fruits for OP accessions, and variable fruits for bagged accessions. Asterisks indicate significant differences between bagged and OP fruits (*, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01, Student’s test).</p>
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<p>Comparison of quality traits between fruits derived from open-pollinated (OP) and bagged flowers. (<b>A</b>) Fruit firmness, soluble sugar content and starch index were measured for 16 parthenocarpy accessions. (<b>B</b>) Fruit firmness, soluble sugar content and starch index were measured for 18 self-compatible accessions. Starch pattern index was visually match to the standard ground colour chart (ENZA International, New Zealand). The error bars present SE of three fruits for OP accessions, and variable fruits for bagged accessions.</p>
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<p>Comparison of quality traits between fruits derived from open-pollinated (OP) and bagged flowers. (<b>A</b>) Fruit firmness, soluble sugar content and starch index were measured for 16 parthenocarpy accessions. (<b>B</b>) Fruit firmness, soluble sugar content and starch index were measured for 18 self-compatible accessions. Starch pattern index was visually match to the standard ground colour chart (ENZA International, New Zealand). The error bars present SE of three fruits for OP accessions, and variable fruits for bagged accessions.</p>
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<p>The principal component analysis (PCA) represents the genetic distance of accessions used in this survey based on SNP markers.</p>
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<p>Genome-wide association study (GWAS) analysis for parthenocarpy and self-compatibility. (<b>A</b>,<b>B</b>) The quantile–quantile (Q–Q) plots of parthenocarpy trait (<b>A</b>) and self-compatible trait (<b>B</b>). The red line indicates the observed <span class="html-italic">p</span> &lt; 0.001 threshold and the black line indicates the expected threshold. (<b>C</b>,<b>D</b>) The Manhattan plot shows the level of significance for SNPs correlated with parthenocarpy trait (<b>C</b>) and self-compatible (<b>D</b>) trait from the GWAS analysis (numbers across the <span class="html-italic">x</span>-axis indicate the chromosome). The black dashed lines represent the threshold −log10(<span class="html-italic">p</span>)  ≥  3.0.</p>
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12 pages, 341 KiB  
Article
Agromorphological Evaluation of Elite Lines of Native Tomato (Solanum lycopersicum L.) from Central and Southern Mexico
by María Concepción Valencia-Juárez, Enrique González-Pérez, Salvador Villalobos-Reyes, Carlos Alberto Núñez-Colín, Jaime Canul-Ku, José Luis Anaya-López, Elizabeth Chiquito-Almanza and Ricardo Yáñez-López
Agronomy 2024, 14(12), 2829; https://doi.org/10.3390/agronomy14122829 - 27 Nov 2024
Viewed by 203
Abstract
Tomato (Solanum lycopersicum L.) is one of the most important cultivated vegetables in the world. However, in some countries such as Mexico the lack of cultivars adapted to different environmental production conditions is a limitation. Moreover, recent studies have indicated that breeding [...] Read more.
Tomato (Solanum lycopersicum L.) is one of the most important cultivated vegetables in the world. However, in some countries such as Mexico the lack of cultivars adapted to different environmental production conditions is a limitation. Moreover, recent studies have indicated that breeding aimed at increasing yield has led to a loss of genetic diversity. Therefore, it is necessary to explore and characterize new sources of germplasms. This study aimed to characterize new sources of germplasm and identify the most transcendental traits for distinguishing tomato types and lines that are useful for the genetic improvement of the species. Sixty characters were evaluated in 16 advanced lines of native tomatoes from Central and Southern Mexico during the fall–winter cycles 2023–2024 at the Bajío Experimental Station, Celaya, Guanajuato, Mexico, based on the guidelines of the International Union for the Protection of New Varieties of Plants (UPOV) and the International Plant Genetic Resources Institute (IPGRI). The data were analyzed using descriptive statistics, analysis of variance and post hoc tests, canonical discriminant analysis, and the Eigenanalysis selection index method (ESIM). Morphological variation showed that five qualitative traits were determinant factors in distinguishing tomato types and lines, whereas agronomic discriminant traits were the equatorial and polar diameters of the fruit and its ratio, number of locules, pedicel length, stem length, and internode distance. In addition, significant positive correlations were found between leaf length and width, equatorial diameter of the fruit, and polar diameter of the fruit. Lines JCM-17, JMC-10, and JCM-01 were the most selectable lines according to the ESIM values. The morphological variation found and the characteristics with higher selection values identified may be valuable for optimizing the tomato genetic improvement process in general. Full article
17 pages, 1070 KiB  
Article
The Effect of Nighttime LED Lighting on Tomato Growth, Yield, and Nutrient Content of Fruits
by Inna V. Knyazeva, Olga Panfilova, Oksana Vershinina, Alexander A. Smirnov, Alexey S. Dorokhov and Ibrahim Kahramanoğlu
Horticulturae 2024, 10(12), 1259; https://doi.org/10.3390/horticulturae10121259 - 27 Nov 2024
Viewed by 229
Abstract
Food insecurity is a top economic and national security concern in many countries, and scientists worldwide are working to increase crop productivity in order to address this issue. In line with this information, the present study aimed to test the possibility of improving [...] Read more.
Food insecurity is a top economic and national security concern in many countries, and scientists worldwide are working to increase crop productivity in order to address this issue. In line with this information, the present study aimed to test the possibility of improving the yield and fruit quality of two tomato cultivars, namely ‘Vspyshka’ and ‘Lyana’. The effect of LSL (light of sodium lamps—control) and the short additional 4 h treatment of nighttime LED lighting (LSL+night LED) with an increase in the proportion of red, blue, and far-red spectra on tomato fruit yield as well as its physiological, biochemical, and consumer attributes were compared in this study. The results suggested that LSL+night LED significantly increased soluble solids concentration, vitamin C content, and polyphenolic compounds of tomato fruits, taking into account the varietal characteristics. Moreover, a moderate to high relationship was also observed between the polyphenolic complex, vitamin C content, and antioxidant activity. It was concluded that the LSL+night LED could further enhance the relationship between polyphenols and antioxidants, as well as soluble solids concentration. LSL+night LED treatment also provided an increased accumulation of five essential amino acids associated with the taste characteristics of fruits, namely histidine, valine, threonine, licin, and the sum of isoleucine. In addition, the contents of lysine and methionine increased in the ‘Lyana’ cultivar. LSL+night LED treatment was also noted to have a less pronounced effect on the contents of aspartic acid and asparagine, as bio stimulators of plant growth processes, as well as the amino acids arginine, serine, glycine, and tyrosine, which were additionally consumed to restore photosynthesis. LSL+night LED treatment reduced the concentration of nitrates in fruits, which is a toxic element for human health. Overall, the results of the study are believed to be demanded in practical applications, with potential benefits in improving the elements of resource-saving technology for growing vegetable crops. Full article
12 pages, 3726 KiB  
Article
Comparative Transcriptome Analysis Reveals a Tissue-Specific Pathway Involved in Nitrogen Utilization Between Genotypes with Different Nitrogen Use Efficiencies in Tea Plants (Camellia sinensis)
by Min Wang, Kangwei Sun, Xujun Qin, Shuting Gong, Zhipeng Li and Kai Fan
Agronomy 2024, 14(12), 2824; https://doi.org/10.3390/agronomy14122824 - 27 Nov 2024
Viewed by 249
Abstract
Nitrogen (N) is a key nutrient which affects plant development and quality formation for tea plants. Notable genetic variation in nitrogen use efficiency (NUE) has been reported among different genotypes of Camellia sinensis. However, the molecular mechanisms underlying these differences have not [...] Read more.
Nitrogen (N) is a key nutrient which affects plant development and quality formation for tea plants. Notable genetic variation in nitrogen use efficiency (NUE) has been reported among different genotypes of Camellia sinensis. However, the molecular mechanisms underlying these differences have not been illuminated. In this study, a 15N tracing method was used to compare nitrogen use efficiency among six genotypes. The results show that there were significant differences in the NUEs among these genotypes. Among them, TC12 had the highest NUE, while LJCY had the lowest NUE. Transcriptome analysis between these two cultivars showed that differentially expressed genes (DEGs) were significantly enriched in photosynthesis—antenna proteins and zeatin biosynthesis in mature leaves and new shoots, respectively. TC12 had higher expression levels of AMT1.2, NRT2.4, and NRT3.2 in the roots, AAP6 and AAP7 in the stems and shoots, and LHC in the mature leaves than LJCY. The expression of ZOG1 and CKX, which are involved in zeatin biosynthesis, was down-regulated in the shoots of TC12 compared with LJCY. These findings will contribute to insights into the molecular mechanism of nitrogen utilization and the identified candidate genes provide a genetic resource for improving N use efficiency in tea plants. Full article
(This article belongs to the Section Horticultural and Floricultural Crops)
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<p>Comparison of nitrogen use efficiency among different tea cultivars. (<b>a</b>) N<sub>dff</sub> in different tissues; (<b>b</b>) <sup>15</sup>N accumulation in different tissues; (<b>c</b>) NUEs among different tea cultivars. The error bars indicate the standard deviations and the values corresponding to the mean ± standard deviation (SD) of three independent biological replicates. Different letters indicate significant difference (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Functional annotation classification for unigenes. (<b>a</b>) GO enrichment analysis for unigenes; (<b>b</b>) KOG enrichment analysis for unigenes; (<b>c</b>) KEGG enrichment analysis for unigenes. The red rectangle means the most enriched category.</p>
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<p>Enrichment of DEGs for the top 20 KEGG pathways in different tissues. (<b>a</b>) Roots; (<b>b</b>) stems; (<b>c</b>) leaves; and (<b>d</b>) new shoots. The red dotted rectangles means the most significantly encirched pathways.</p>
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<p>Expression profiles of DEGs involved in nitrogen uptake and transport in different tissues between the two cultivars. (<b>a</b>) Ammonium and nitrate transporter; (<b>b</b>) amino acid transporter.</p>
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<p>Expression profiles of DEGs involved in photosynthesis in different tissues between the two cultivars. (<b>a</b>) <span class="html-italic">LHCB</span>; (<b>b</b>) <span class="html-italic">LHCB</span> in tea leaves.</p>
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<p>Expression profiles of DEGs involved in cytokinin metabolism in different tissues between the two cultivars.</p>
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14 pages, 1522 KiB  
Article
Modeling the Effects of Sowing Dates on Maize in Different Environments in the Tropical Area of Southwest China Using DSSAT
by Wenfeng Li, Wenrong Liu, Yue Huang, Weihua Xiao, Lei Xu, Kun Pan, Guodong Fu, Xiuyue Chen and Chao Li
Agronomy 2024, 14(12), 2819; https://doi.org/10.3390/agronomy14122819 - 27 Nov 2024
Viewed by 148
Abstract
Maize yield is affected by meteorological conditions and cultivation management. Sowing date adjustment is one of the most commonly used cultivation management methods for achieving a high maize yield in the tropical area of Southwest China. This study conducted field experiments involving five [...] Read more.
Maize yield is affected by meteorological conditions and cultivation management. Sowing date adjustment is one of the most commonly used cultivation management methods for achieving a high maize yield in the tropical area of Southwest China. This study conducted field experiments involving five maize cultivars with different sowing dates in Yunnan Province from 2012 to 2015. The parameters of the CERES model in the decision support systems for agrotechnology transfer (DSSAT) were calibrated, and its adaptability was validated. The model was applied to simulate and analyze the maize growing period and yield with different sowing dates over 12 years (2012–2023) in the tropical area of Southwest China. The results show that the DSSAT-Maize model demonstrates good adaptability in the southwestern region of China. The model predictions for maize flowering, maturity, and yield were compared with the measured values, yielding R2 values of 0.62, 0.64, and 0.92, d-index values of 0.86, 0.87, and 0.97, and normalized root-mean-square errors (nRMSEs) of 4.53%, 2.92%, and 6.37%, respectively. The verified model was used to assess the effects of different sowing dates on the maize growing period and yield. Sowing between 15 May and 29 May resulted in relatively higher yields with lower coefficients of variation. The whole growing season was shortened by 1.13 days, and the yield was decreased by 3% every 7 days ahead of the sowing date before early May. A delayed planting date after June had a positive effect on maize yields, with an average yield increase of 4% per 7 days of delay. The maize yield was significantly positively correlated with rainfall during the vegetative period and solar radiation during the reproductive period; meanwhile, it was significantly negatively correlated with solar radiation and the maximum temperature during the vegetative period and rainfall during the reproductive period. This study concluded that the sowing date significantly influenced maize’s growth period and yield in the tropical area of Southwest China. Delaying sowing after 15 May can help achieve higher yields, mainly because early sowing leads to insufficient rainfall in the vegetative period, while delayed sowing ensures adequate rainfall and higher total solar radiation. Full article
(This article belongs to the Section Precision and Digital Agriculture)
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<p>Study station locations.</p>
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<p>Comparison of measured and simulated values for days from sowing to flowering (<b>a</b>), days from sowing to maturity (<b>b</b>), and grain yield (<b>c</b>).</p>
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<p>The duration of days from sowing to flowering and maturity for maize sown on various dates. Note: each box plot is based on 13 years of meteorological data to simulate the growth period. The upper and lower limits of each box are the upper and lower quartiles of the data, respectively. ▲ represents the average of the data.</p>
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<p>Prediction results of maize yield using DSSAT model on different planting dates of 5 maize cultivars from 2012 to 2023. Note: the blue dashed line represents the average yield for all sowing periods in all years. ▲ represents the average of the data.</p>
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<p>Coefficients of variation of maize yield predicted using DSSAT model for sowing dates from 2012 to 2023.</p>
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<p>Box plot distribution of solar radiation, maximum temperature, minimum temperature, and total rainfall during vegetative period, reproductive period, and whole growth period of maize on each planting date from 2012 to 2023. ▲ represents the average of the data.</p>
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18 pages, 4224 KiB  
Review
Genetic Insights and Molecular Breeding Approaches for Downy Mildew Resistance in Cucumber (Cucumis sativus L.): Current Progress and Future Prospects
by Ewa Mirzwa-Mróz, Bartłomiej Zieniuk, Zhimin Yin and Magdalena Pawełkowicz
Int. J. Mol. Sci. 2024, 25(23), 12726; https://doi.org/10.3390/ijms252312726 - 27 Nov 2024
Viewed by 256
Abstract
Cucurbit downy mildew, caused by Pseudoperonospora cubensis, is a devastating disease in cucumbers that leads to significant yield losses in many cucurbit-growing regions worldwide. Developing resistant cucumber varieties is a sustainable approach to managing this disease, especially given the limitations of chemical [...] Read more.
Cucurbit downy mildew, caused by Pseudoperonospora cubensis, is a devastating disease in cucumbers that leads to significant yield losses in many cucurbit-growing regions worldwide. Developing resistant cucumber varieties is a sustainable approach to managing this disease, especially given the limitations of chemical control and the evolving nature of pathogens. This article reviews the genetic basis of downy mildew resistance in cucumbers, emphasizing key resistance (R) genes and quantitative trait loci (QTLs) that have been mapped. Recent advances in molecular breeding tools, including marker-assisted selection (MAS), genomic selection (GS), and CRISPR/Cas9 genome editing, have accelerated the development of resistant cultivars. This review also explores the role of transcriptomics, genomics, and other ‘omics’ technologies in unraveling the molecular mechanisms behind resistance and offers insights into the future of breeding strategies aimed at long-term disease management. Management strategies for cucurbit downy mildew are discussed, along with the potential impacts of climate change on the occurrence and severity of downy mildew, highlighting how changing environmental conditions may influence disease dynamics. Integrating these advanced genetic approaches with traditional breeding promises to accelerate the development of downy mildew-resistant cucumber varieties, contributing to the sustainability and resilience of cucumber production. Full article
(This article belongs to the Special Issue Molecular Biology of Cucurbitaceae Family Plants)
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<p>Symptoms of cucurbit downy mildew on cucumber: (<b>a</b>) chlorotic lesions on the upper leaf surface restricted by leaf veins, (<b>b</b>) spots soaked with water on the underside of the leaf, (<b>c</b>) magnification of spots soaked with water, (<b>d</b>) chlorotic and yellow lesions on the upper leaf surface, (<b>e</b>) brown, necrotic spots, (<b>f</b>) merging necrotic spots, (<b>g</b>) upward leaf curling, and (<b>h</b>) dying plants (Photos C. Zamorski).</p>
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<p>Symptoms of cucurbit downy mildew on cucumber: (<b>a</b>) chlorotic lesions on the upper leaf surface restricted by leaf veins, (<b>b</b>) spots soaked with water on the underside of the leaf, (<b>c</b>) magnification of spots soaked with water, (<b>d</b>) chlorotic and yellow lesions on the upper leaf surface, (<b>e</b>) brown, necrotic spots, (<b>f</b>) merging necrotic spots, (<b>g</b>) upward leaf curling, and (<b>h</b>) dying plants (Photos C. Zamorski).</p>
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<p>Sporulation of <span class="html-italic">P. cubensis</span> on the underside of the leaf: (<b>a</b>) sporangiophore and (<b>b</b>) dark sporangia (Photos E. Mirzwa-Mróz).</p>
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<p>Life cycle of <span class="html-italic">P. cubensis</span>.</p>
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12 pages, 2687 KiB  
Article
Non-Destructive Monitoring of External Quality of Date Palm Fruit (Phoenix dactylifera L.) During Frozen Storage Using Digital Camera and Flatbed Scanner
by Younes Noutfia, Ewa Ropelewska, Zbigniew Jóźwiak and Krzysztof Rutkowski
Sensors 2024, 24(23), 7560; https://doi.org/10.3390/s24237560 - 27 Nov 2024
Viewed by 294
Abstract
The emergence of new technologies focusing on “computer vision” has contributed significantly to the assessment of fruit quality. In this study, an innovative approach based on image analysis was used to assess the external quality of fresh and frozen ‘Mejhoul’ and ‘Boufeggous’ date [...] Read more.
The emergence of new technologies focusing on “computer vision” has contributed significantly to the assessment of fruit quality. In this study, an innovative approach based on image analysis was used to assess the external quality of fresh and frozen ‘Mejhoul’ and ‘Boufeggous’ date palm cultivars stored for 6 months at −10 °C and −18 °C. Their quality was evaluated, in a non-destructive manner, based on texture features extracted from images acquired using a digital camera and flatbed scanner. The whole process of image processing was carried out using MATLAB R2024a and Q-MAZDA 23.10 software. Then, extracted features were used as inputs for pre-established algorithms–groups within WEKA 3.9 software to classify frozen date fruit samples after 0, 2, 4, and 6 months of storage. Among 599 features, only 5 to 36 attributes were selected as powerful predictors to build desired classification models based on the “Functions-Logistic” classifier. The general architecture exhibited clear differences in classification accuracy depending mainly on the frozen storage period and imaging device. Accordingly, confusion matrices showed high classification accuracy (CA), which could reach 0.84 at M0 for both cultivars at the two frozen storage temperatures. This CA indicated a remarkable decrease at M2 and M4 before re-increasing by M6, confirming slight changes in external quality before the end of storage. Moreover, the developed models on the basis of flatbed scanner use allowed us to obtain a high correctness rate that could attain 97.7% in comparison to the digital camera, which did not exceed 85.5%. In perspectives, physicochemical attributes can be added to developed models to establish correlation with image features and predict the behavior of date fruit under storage. Full article
(This article belongs to the Special Issue Artificial Intelligence and Key Technologies of Smart Agriculture)
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<p>Experimental design for frozen date fruit under storage. MEJ: ‘Mejhoul’; BFG: ‘Boufeggous’; FRZ10: freezing at −10 °C; M0: month 0; Cam: camera; Scan: scanner.</p>
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<p>Logical flowchart for date fruit image processing and analysis.</p>
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<p>Illustration of background images and their respective ROIs for ‘Mejhoul’ (<b>a</b>) and ‘Boufeggous’ (<b>b</b>) cultivars.</p>
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<p>Accuracy rates obtained using the flatbed scanner and digital camera for discrimination between frozen date samples under different temperatures.</p>
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<p>Confusion matrix, ROC area, and RRSE of freeze-stored ‘Mejhoul’ and ‘Boufeggous’ cultivars obtained using a flatbed scanner (<b>a</b>) and digital camera (<b>b</b>).</p>
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<p>Classification correctness between fresh and freeze-stored date fruit at 2, 4, and 6 months at −10 °C and −18 °C for ‘Mejhoul’ samples acquired with (<b>a</b>) a digital camera and (<b>b</b>) flatbed scanner and ‘Boufeggous’ samples acquired with (<b>c</b>) a digital camera and (<b>d</b>) flatbed scanner.</p>
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