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8 results for “flower volatiles”
Fig. 1 in Differences in volatile composition and sexual morphs in rambutan (Nephelium lappaceum L.) flowers and their effect in the Apis mellifera L. (Hymenoptera, Apidae) attraction
Fig. 1. Relation between compounds in rambutan hermaphrodite flowers from Herradero (Her RH) and Metapa orchard (Her RM), and male flowers (Male RH).
Haplopappus floral volatiles, flower visitors' preferences, and floral-visitors interaction outcomes along an Andean elevational gradient
Open the record for dataset details and reuse information.
Fig. 3 in Profiling of volatile and non-volatile metabolites in Polianthes tuberosa L. flowers reveals intraspecific variation among cultivars
Fig. 3. Soluble and wall-bound phenolics profile of tuberose cultivars. Histogram A shows the amount of rutin determined by UHPLC analysis in ng g −1 fr. wt of flower tissue, and B shows the amount of caffeic acid, p-coumaric acid and ferulic acid in ng mg−1 pellet dry wt of. Note: All values are mean ± s.d. of three replicates.
Fig. 2 in Profiling of volatile and non-volatile metabolites in Polianthes tuberosa L. flowers reveals intraspecific variation among cultivars
Fig. 2. Heat map representing the diversity of nonvolatile compounds detected in P. tuberosa flowers. Floral extracts after derivatization were analysed by GC-MS. Classes 0, 1, 2, 3, 4, 5, and 6 indicates group average abundances of Calcutta double, Calcutta single, Jyothi, Ujwal, Shnigdha, Shringhar, and Phule rajani cultivars respectively. Red and green color denotes highest and lowest relative abundances of non-volatile compounds, respectively. Abbreviations: Met a-D-gal - Methyl α-D-galactofuranoside, Met b-D-gal - Methyl β-D-galactopyranoside, Met b-D-glu - Methyl β-D-glucofuranoside, 4- HBALD - 4-hydroxybenzaldehyde, 4-HBA - 4-hydroxybenzoic acid, 2, 5-DHBA - 2, 5-Dihydroxybenzoic acid. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5 in Profiling of volatile and non-volatile metabolites in Polianthes tuberosa L. flowers reveals intraspecific variation among cultivars
Fig. 5. Metabolite map representing the normalized relative abundances of few important primary and specialized metabolites during the blooming stage of P. tuberosa flowers. The amount of metabolites from four different P. tuberosa cultivar clusters were colour coded for low to high contents as per the scale shown. Cluster A includes CD, cluster B includes CS, cluster C includes JY and PR and cluster D includes SN, UJ, and SR. Solid arrows represent single step reactions, dotted arrows represent multi step reactions and block arrows represent volatile emission or exchange within the cell. Emitted levels of volatiles are shown outside the cell, while endogenous levels are represented inside the cytosol. Glycosyl-bound volatiles are shown inside in a representative vacuolar structure. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Profiling of volatile and non-volatile metabolites in Polianthes tuberosa L. flowers reveals intraspecific variation among cultivars
Fig. 1. Profile of floral scent volatiles in studied cultivars of P. tuberosa. Stack plots represent (A) volatiles emitted by flowers in μg g−1 fr. wt h−1, (B) free endogenous volatiles of whole flower in μg μg g−1 fr. wt and (C) glycosyl-bound volatiles of whole flower in μg μg g−1 fr. wt. Abbreviations: CD - Calcutta double, CS - Calcutta single, JY - Jyothi, UJ - Ujwal, SN - Shnigdha, SR - Shringhar, and PR - Phule rajani.
Fig. 4 in Profiling of volatile and non-volatile metabolites in Polianthes tuberosa L. flowers reveals intraspecific variation among cultivars
Fig. 4. Multivariate analysis of P. tuberosa cultivars (classes 0–6). The scores plot obtained after PLS-DA analysis has been shown in A, where components 1 and 2 together can explain the maximum variance between the cultivars. Metabolites having higher VIP scores are shown in B where their relative abundances are color coded from high to low as per the scale shown. The dendrogram as shown in C was obtained after hierarchical clustering analysis of studied P. tuberosa cultivars. Classes 0, 1, 2, 3, 4, 5, and 6 represent Calcutta double, Calcutta single, Jyothi, Ujwal, Shnigdha, Shringhar and Phule rajani cultivars. Metabolites enlisted as 1–25 in B are sequentially represented as follows: quinic acid, V_D-limonene (V: detected as emitted volatile), myo-inositol, D-mannose, V_3-carene, EV_cis-methyl eugenol (EV: detected as endogenous volatile), V_Z- β-caryophyllene, V_benzyl salicylate, EV_benzyl benzoate, EV_eugenol, methyl α-D-galactofuranoside, EV_(Z, E)-farnesol, GV_2-nitrocumene (GV: detected as glycosyl-bound volatile), EV_1,8-cineole, V_1,R-α-pinene, Methyl β-D-galactopyranoside, GV_4-propyl benzaldehyde, Methyl α-Dglucofuranoside, V_β-terpineol, D-fructofuranose, L-threonine, EV_2-hydroxy cineole, EV_3-exo-hydroxy-1,8-cineole, EV_5-hydroxy-7(Z)-decenoic acid-δ-lactone and GV_5-hydroxy-7Z-decenoic acid- δ –lactone.
Honey bee foraging decisions are influenced by pear flower volatiles
<p>Data of honey bee foraging bias on pear flowers.</p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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