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778 results for “TOMATO”
Data from: Reproductive phenology of the tomato frog, Dyscophus antongili, in an urban pond of Madagascar's east coast
Based on daily monitoring around an urban pond in the coastal town of Maroantsetra, from 2003-2011, we provide an analysis of the yearly reproductive activity of the tomato frog (Dyscophus antongilii), a large-sized and prominent red-coloured microhylid frog from north-eastern Madagascar. Frogs were observed all year round but despite the lack of limited climatic seasonality in the region it was possible to observe a high activity period between January-May and a lower activity period between June-December. Freshly laid eggs were found in all months except November, and with highest incidence between January and May, while calling was heard in all months. We found a positive correlation between daily adult counts and minimum air temperature. On the contrary rainfall did not significantly predict activity, although boosts of calling and egg-laying especially in the austral winter were observed after heavy rainfall events. We define D. antongilii in Maroantsetra as a sporadic wet season breeder that reproduces at irregular intervals following heavy rain events.
FIGURE 1 in A new pest of tomato and other records of mealybugs (Hemiptera: Pseudococcidae) from Espírito Santo, Brazil
FIGURE 1. Typical live appearance of the adult female of P. solenopsis and infested tomato with associated symptoms of deformation and distortion of the terminal growth; A, twisting and curling of stems; B, leaf wrinkling and puckering (photographs January 2005, Manguinhos, ES, MPC).
Resequenced tomato MAGIC population parents
<p>The file Sl_MAGIC_population_parents_resequencing.vcf.gz provides the variants of eight highly diverse wild and weedy S. pimpinellifolium (BGV006454, BGV015382, BGV013720 and BGV007145 ) and S. lycopersicum var. cerasiforme (BGV006769, BGV007931, LA2251 and PI487625 ) accessions, which are the parents of a MAGIC population that is currently under development.<br> All the detailed information can be found in the following publication:<br> Gramazio, Pietro, et al. "Morphoagronomic characterization and whole-genome resequencing of eight highly diverse wild and weedy S. pimpinellifolium and S. lycopersicum var. cerasiforme accessions used for the first interspecific tomato MAGIC population." Horticulture Research 7.1 (2020): 1-16.</p>
FIGURE 1 in A new species of the genus Asobara Foerster (Hymenoptera: Braconidae) parasitic on Zeugodacus cucurbitae (Coquillett) (Diptera: Tephritidae) infesting tomato in India
FIGURE 1. Asobara jenningsi Gupta sp. nov. (female) A. Habitus (in dorsal view); Habitus (in lateral view).
FIGURE 2 in A new species of the genus Asobara Foerster (Hymenoptera: Braconidae) parasitic on Zeugodacus cucurbitae (Coquillett) (Diptera: Tephritidae) infesting tomato in India
FIGURE 2. Asobara jenningsi Gupta sp. nov. (female) A. Head, dorsal view, B. Head, frontal view, C. Mesopleuron, D. Fore wing, E. Hind wing, F. Mesosoma, G. Metasoma, H. Propodeum.
Supplementary Data for: Intraspecific diversity in the wild tomato species Solanum chilense in initial immune responses towards a glucan elicitor
<p>This repository contains:</p> <p>Read count data for the RNASeq as reported in the paper</p> <p>) All scripts used for the RNASeq analysis</p> <p> </p> <p>) a table describing DEGs with known homologous gene</p> <p> </p> <p>) a table describing DEGs with known homologous genes</p> <p><br> ) All data underlying the graphs related to the quantification of defence responses and plotting the result, sorted by figure.</p>
Inoculation of tomato plant by tomato ringspot virus (ToRSV)
<p>This movie shows inoculation of the lower leaves of the tomato plants with an age of 5 weeks by tomato ringspot virus (ToRSV).</p>
Fig. 2 in The esterification of xanthophylls in Solanum lycopersicum (tomato) chromoplasts; the role of a non-specific acyltransferase
Fig. 2. Example chromatograms showing the effect of the pyp mutation on azygous and ketocarotenoid fruit. 1) Astaxanthin, 2) Lutein, 3) Phoenicoxanthin, 4) Canthaxanthin, 5) 3′OH Echinenone, 6) 3OH Echinenone, 7) Echinenone, 8 and 8′) Lycopene, 9) Esterified carotenoid, 10) γ-Carotene, 11) Esterified carotenoid, 12) β-Carotene.
Fig. 1 in The esterification of xanthophylls in Solanum lycopersicum (tomato) chromoplasts; the role of a non-specific acyltransferase
Fig. 1. Workflow for the generation, screening and phenotypic observations of the four genotypes created. Blue circles indicate number of genotypes detected from the total pool used.
Fig. 3 in The esterification of xanthophylls in Solanum lycopersicum (tomato) chromoplasts; the role of a non-specific acyltransferase
Fig. 3. Biosynthetic pathway of ketocarotenoids and ketocarotenoid esters. CRTZ and CRTW are the bacterial carotenoid hydroxylase and oxygenase enzymes respectively. The PYP gene facilitates the esterification with fatty acids to generate ketocarotenoid esters. Phoenicoxanthin and astaxanthin accumulate within the genotypes assessed and esterified forms of these have been observed in this work.
Fig. 3. A in Bio-genetic analysis of resistance in tomato to early blight disease, Alternaria alternata
Fig. 3. A two-dimensional plot of the Principal Component Analysis (PCA) of ISSR data showing the clustering of 35 tomato genotypes. On PCA plot, three groups are formed and two other genotypes, namely 111 Falat American and Roma, scattered on the plot and do not fall under any of the groups. The distribution of genetic variation within, and among, groups, was detected using the molecular variance analysis (AMOVA) in GenAlEx software. Genetic variation indices, including observed number of alleles (Na) and effective numbers of alleles (Ne), Shannon's information index (I), Nei's gene diversity (H), percent of polymorphic loci (PPL), were estimated using POP-GENE software.
Fig. 1 in Bio-genetic analysis of resistance in tomato to early blight disease, Alternaria alternata
Fig. 1. Ward's clustering dendrogram of 35 tomato genotypes based on resistance to Alternaria alternata. Note: Cluster Ӏ consisted of moderately susceptible and moderately resistant genotypes, Cluster ӀӀ consisted of resistant genotypes and Cluster ӀӀӀ consisted of highly susceptible genotypes. Disease severity was assessed based on infection percent (0–100) against the scoring scales of: 0, 5, 10, 25, 50, 75, or 100%.
Fig. 2 in Bio-genetic analysis of resistance in tomato to early blight disease, Alternaria alternata
Fig. 2. Grouping of 35 tomato genotypes and lines using the UPGMA method based on complete algorithm and Jaccard's similarity coefficient of 11 ISSR molecular markers. G1 consisted of highly susceptible genotype, G2 consisted of susceptible genotype, G3 consisted of moderately susceptible genotype, G4 consisted of moderately resistant genotype and G5 consisted of resistant genotype. Pearson correlation analysis was carried out to analyze the relationship among the tomato genotypes and response variability and cluster analysis of data was performed using SPSS software.
Fig. 4 in Glandular trichome-derived sesquiterpenes of wild tomato accessions (Solanum habrochaites) affect aphid performance and feeding behavior
Fig. 4. Effect of pure β-caryophyllene and α-humulene on M. euphorbiae feeding performance (A–C) and choice behavior (D). Different amounts of a mix of pure β-caryophyllene and α-humulene (3:1 ratio) were added to the feeding diet. The data in (A), (B), and (C) show the comparison of Kaplan-Meier survival curves (logrank test, α =0.05), gel saliva density (Tukey's HSD, α =0.05), and number of honeydew drops (ANOVA, α = 0.05), respectively, upon addition of different amounts of pure sesquiterpenes to the artificial diet. The data in (D) represent the behavioral responses of aphid alatae to odors from leaves of c.v. M82 alone (right bars) or from leaves of c.v. M82 leaves in combination with different amounts of a mix of pure β-caryophyllene and α-humulene (left bars) (Chi-square goodness of fit; *, P <0.05; **, P <0.01).
Fig. 5 in Glandular trichome-derived sesquiterpenes of wild tomato accessions (Solanum habrochaites) affect aphid performance and feeding behavior
Fig. 5. α-Santalene and α-bergamotene producing tomato introgression line affects performance, feeding and choice behavior of M. euphorbiae. (A) Performance of M. euphorbiae apterae arrested on the leaf surface of S. lycopersicum LA4024, S. habrochaites LA1777, and the introgression lines LA3935, LA3934, LA3936, and LA3937. Values for longevity and fecundity are presented as mean ± SE and compared by Tukey's HSD test (α =0.05). (B) Kaplan-Meier estimates of survivorship of M. euphorbiae apterae feeding on artificial diets containing leaf dip extracts of S. lycopersicum LA4024, S. habrochaites LA1777, and the introgression line LA3935 (logrank test, α = 0.05). (C) and (D) Box plots represent means ± SE of gel saliva density (cm 2) and number of honeydew drops, respectively. Tukey's HSD tests (α = 0.05) are used for post-hoc analysis. (E) Choice of M. euphorbiae alatae between odors from LA4024 leaves alone (left bars) and from LA4024 leaves with added leaf dip extracts (100 and 300 μL) from the introgression line LA3935 or S. habrochaites LA1777 (right bars) (Chi-square goodness of fit; *, P <0.05; **, P <0.01).
Fig. 3 in Glandular trichome-derived sesquiterpenes of wild tomato accessions (Solanum habrochaites) affect aphid performance and feeding behavior
Fig. 3. Choice behavior of M. euphorbiae alatae in an open Y-track olfactometer. (A) Choice of aphids between air and odors from leaves of different S. lycopersicum cultivars or S. habrochaites accessions. (B) Choice of aphids between odors from leaves of c.v. M82 and different S. habrochaites accessions. (C) Choice of aphids between odors from leaves of c.v. M82 leaves alone (left bars) and from leaves of c.v. M82 leaves with added S. habrochaites leaf dip extracts (right bars). Asterisks following each pair of bars indicates significant differences according to Chi-square goodness of fit (⋅, P <0.07; *, P <0.05; **, P <0.01).
Fig. 2 in Glandular trichome-derived sesquiterpenes of wild tomato accessions (Solanum habrochaites) affect aphid performance and feeding behavior
Fig. 2. Feeding performance of M. euphorbiae apterae on artificial diets containing leaf dip extracts of S. lycopersicum c.v. M82 and different S. habrochaites accessions (MTBE solvent control). (A) Kaplan-Meier estimates of survivorship and analysis of log-rank test (α =0.05). (B) Box and violin plots represent mean ± SE of gel saliva density (cm 2) and the probability density, respectively. (C) Number of honeydew drops accumulated in the feeding chambers. Asterisks in (B) and (C) represent significant differences between diets with leaf dip extracts and control based on Dunnett's test (⋅, P <0.08; *, P <0.05; **, P <0.01; ***, P <0.001).
Fig. 1 in Glandular trichome-derived sesquiterpenes of wild tomato accessions (Solanum habrochaites) affect aphid performance and feeding behavior
Fig. 1. Longevity (A) and fecundity (B) of M. euphorbiae apterae arrested on the leaf surface of two S. lycopersicum cultivars and different S. habrochaites accessions. Solanum habrochaites accessions represent five chemotypes characterized by the production of different sesquiterpenes in their glandular trichomes. Values for longevity and fecundity are presented as mean ± SE. Different letters indicate that logarithmic values were significantly different (Tukey's HSD test, α = 0.05).
The dataset of Tomato
<p>This dataset contains <strong>895 images</strong> with <strong>bounding box annotations</strong> provided in PASCAL VOC format for the creation of detection models.<br> All annotations belong to a single class: tomato.</p> <p>A link to the original dataset: https://www.kaggle.com/datasets/andrewmvd/tomato-detection</p> <p>We randomly divided it into new training set, verification set and test set in a ratio close to 7:2:1.</p>
Effects of Tomato Consumption on Steatosis, Intestinal Function and Glucose and Lipid Metabolism in Subjects With NAFLD
ClinicalTrials.gov study NCT06389851. IPD Sharing: NO. Countries: 1. Publications: 4.
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