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26 results for “Dianthus caryophyllus”
Dianthus caryophyllus L. (BR0000015229335V)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Dianthus caryophyllus L. (BR0000010669099)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Dianthus caryophyllus L. (BR0000014449437)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Dianthus caryophyllus L. (BR0000012291656)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Dianthus caryophyllus L. (BR0000014449444)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Dianthus caryophyllus L. (BR0000010120835)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Dianthus caryophyllus L. (BR0000010801895)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Fig. 9 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 9. Effects of hypoxic treatment on earlier responses of gene expression. Relative transcript levels calculated by real-time RT-PCR using DcUbq3-7 as a standard were compared before (black bars) and after 3 or 12 h of incubation under normoxic (gray bars) and hypoxic (white bars) conditions. Significant differences (P <0.05) detected by Tukey's multiple comparison test are indicated by different letters above the bars.
Fig. 5 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 5. Phylogenetic tree of sucrose synthase (SUS). Amino acid sequences deduced from SUS genes of Arabidopsis, rice, and carnation, distinguished by AGI ID, locus identifier, or ORF no. shown in parentheses, were aligned by ClustalW. The tree was constructed by the neighbor-joining method using MEGA7.0 software. * indicates carnation SUS described in this study.
Fig. 8 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 8. Expression profiles of sucrose synthase (SUS) gene family of carnation in petals under sucrose and hypoxic treatments. Relative transcript levels calculated by real-time RT-PCR using DcUbq3-7 as a standard were compared among petals after 24 h of incubation with distilled water (plain bars) or sucrose solution (hatched bars), under normoxic (gray bars) and hypoxic (white bars) conditions. Data are expressed as mean ± SE of three separate samples. The results of two-way analysis of variance (ANOVA) are shown below each graph; NS, *, and ** indicate not significant and significant at P <0.05 and P <0.01, respectively.
Fig. 7 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 7. Expression profiles of invertase (INV) gene family of carnation in petals under sucrose and hypoxic treatments. Relative transcript levels calculated by realtime RT-PCR using DcUbq3-7 as a standard were compared among petals after 24 h of incubation with distilled water (plain bars) or sucrose solution (hatched bars), under normoxic (gray bars) and hypoxic (white bars) conditions. Data are expressed as mean ± SE of three separate samples. The results of two-way analysis of variance (ANOVA) are shown below each graph; NS, *, and ** indicate not significant and significant at P <0.05 and P <0.01, respectively.
Fig. 6 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 6. Expression profiles of invertase (INV) and sucrose synthase (SUS) gene families of carnation among organs. Relative transcript levels of gene families of cellwall INV (A), vacuolar INV (B), cytoplasmic INV (C), and SUS (D) calculated by real-time RT-PCR using DcUbq3-7 as a standard were compared among leaves (dotted bars) and petals (black bars). The graph for the gene with an eminent value is shown as an inset. Data are expressed as mean ± SE of three separate samples. The result of Student's t-test is shown above the bars; NS, *, and ** indicate not significant and significant at P <0.05 and P <0.01, respectively.
Fig. 2 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 2. Sugar content in carnation petals. Contents of reducing sugars (A), sucrose (B), and starch (C) were compared among petals after 24 h of incubation following pretreatment with silver-thiosulfate (STS), and supplied with distilled water (plain bars) or sucrose solution (hatched bars), under normoxic (gray bars) and hypoxic (white bars) conditions. Data are expressed as mean ± SE of three separate samples. The results of two-way analysis of variance (ANOVA) are shown below each graph; NS, *, and ** indicate not significant and significant at P <0.05 and P <0.01, respectively. *** indicates significant difference at P <0.05 detected by Dunnett's test.
Fig. 1 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 1. Effects of chemical treatment on flower senescence of carnation. Carnation florets pretreated with silver-thiosulfate (STS) or incubated with sucrose (Suc, not pretreated with STS) were compared to non-pretreated control florets incubated with distilled water (DW).
Fig. 3 in Comprehensive analysis of sucrolytic enzyme gene families in carnation (Dianthus caryophyllus L.)
Fig. 3. Enzymatic activities of invertase (INV) and sucrose synthase (SUS) in carnation petals. Activities of cell-wall INV (A), vacuolar INV (B), cytoplasmic INV (C), and SUS (D) were compared among petals after 24 h of incubation following pretreatment with silver-thiosulfate (STS), and supplied with distilled water (plain bars) or sucrose solution (hatched bars), under normoxic (gray bars) and hypoxic (white bars) conditions. Data are expressed as mean ± SE of three separate samples. The results of two-way analysis of variance (ANOVA) are shown below each graph; NS and * indicate not significant and significant at P <0.05, respectively.
Fig. 6 in Flavonoid biosynthesis in Dianthus caryophyllus L. is early regulated during interaction with Fusarium oxysporum f. sp. dianthi
Fig. 6. Most-important flavonoids from roots of resistant carnation cultivar (GRC) at 96 h post-inoculation (hpi). (a) Top-ranked rt/m/z features by t-test associated with Fod-inoculated or non-inoculated (control) plants of GRC. The ranking is organized from top to bottom according t-test. Each colored cell on the map the heat map indicates the higher (red) or lower (blue) autoscaled feature intensities. Bold numbers in parenthesis correspond to the annotated features listed in Table 1. (b) Classical receiver operating characteristic (ROC) curves of the three top-ranked features comparing Fod-inoculated/control plants of GRC at 96 hpi. Sensitivity on the y-axis; Specificity on the x-axis. Area-under-the-curve (AUC) in blue. Box-plots of the autoscaled intensity of each selected feature between inoculated and control groups within the dataset are presented at left side of each ROC curve. A horizontal red line in box-plots define the optimal cutoff. (c) Time-course profiles of crossvalidated, top-ranked features of GRC. GRC = red time-course; MSC = green time-course. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 7 in Flavonoid biosynthesis in Dianthus caryophyllus L. is early regulated during interaction with Fusarium oxysporum f. sp. dianthi
Fig. 7. Fod inoculation effect on transcriptional levels of putative genes encoding the CHS, CHI and FLS enzymes (i.e., chi, chs and fls) and gene encoding the MYB11 transcription factor (cmyb11) in carnation roots for 'Golem' resistant (GRC) and 'Mizuki' susceptible (MSC) cultivars. Gene expression levels of Fod-inoculated and non-inoculated (control) carnation plants based on real-time RT-PCR experiments. Box plots for the relative quantification of mRNA to histone (left) and the ratio of inoculated/control mRNA levels (right) for (a) chs, (b) chi, (c) fls, and (d) cmyb11. Green boxes = control GRC; light green boxes = inoculated GRC; Blue boxes = control MSC; light blue boxes = inoculated MSC; red boxes = inoculated/control mRNA level ratio of GRC; purple boxes = inoculated/control mRNA level ratio of MSC. Different letter indicates significant differences for each post-inoculation time examined according to Tukey test (P <0.05). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Flavonoid biosynthesis in Dianthus caryophyllus L. is early regulated during interaction with Fusarium oxysporum f. sp. dianthi
Fig. 4. Important features selected by fold-change (FC) analysis, principal component analysis (PCA) and multivariate empirical bayes approach (MEBA) of carnation samples according to the profiles of constitutive flavonoids from both non-inoculated cultivars. (a) Paired FC analysis with threshold |2| of GCR/MSC ratio as comparison type. UV-based filtered features were labelled retention time–mass/charge ratio (rt/m/z) pairs. A feature was highlighted as significant if this ratio was above/below threshold. Red dots represent features above the threshold and related to GRC; Blue dots represent features below the threshold and related to MSC. (b) PCA-derived 3D-scores plot (81% of explained variance). Cultivars are differentiated by colors (blue = MSC; red = GRC); Sampling times (in h) are differentiated by shapes (circles = 0 h; squares = 12 h; triangles = 24 h; diamonds = 48 h; octagons = 96 h). GRC samples collected at later times (24, 48, and 96 h) are highlighted with the semi-transparent red ellipse. (c) PCA-derived 3D-loadings plot. Each dot represents a feature and the distribution across the 3D-plot is related to its statistical influence on principal components for discriminating the samples. The most-influencing GCR-related features are highlighted the semi-transparent red ellipse. (d) Time-course profiles of those high-ranked features for GRC. GRC = red time-course; MSC = green time-course. (e) Hotelling-T2-ranked features from MEBA. Autoscaled relative abundances per cultivar according to the heat map colors: red = higher; blue = lower. Bold numbers in parenthesis correspond to the annotated features listed in Table 1. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Flavonoid biosynthesis in Dianthus caryophyllus L. is early regulated during interaction with Fusarium oxysporum f. sp. dianthi
Fig. 3. (a) Total Phenolic Content (TPC) and (b) Total Flavonoid Content (TFC) of carnation roots at early times during the 96-h Fod-inoculation in vivo assay. TPC expressed as micrograms of gallic acid equivalents per gram of fresh weight (μg CE/100 g fw). TFC expressed as micrograms of catechin equivalents per gram of fresh weight (μg CE/g fw). Each data point is expressed as mean values ± standard error of the mean (SEM) as vertical bars (n = 3). Different letter indicates significant differences for each post-inoculation time examined according to Tukey test (P <0.05). Carnation cultivars: GRC = 'Golem' resistant cultivar; MSC = 'Mizuki' susceptible cultivar.
Fig. 2 in Flavonoid biosynthesis in Dianthus caryophyllus L. is early regulated during interaction with Fusarium oxysporum f. sp. dianthi
Fig. 2. Vascular wilt severity, expressed as severity index (SI), during the 7- week in vivo assay. Each data point is expressed as mean SI ± standard error of the mean (SEM) as vertical bars (n = 3). Different letter marking each data point indicates significant differences for each post-inoculation time examined according to Tukey test (P <0.05). Carnation cultivars: GRC = 'Golem' resistant cultivar; MSC = 'Mizuki' susceptible cultivar.
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Allen Brain Atlas
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International Brain Laboratory public data
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