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382 results for “Citrus”
Fig. 1 in The effectiveness of fruit bagging and culling for risk mitigation of fruit flies affecting citrus in China: a preliminary report
Fig. 1. Five culling procedures for quality control and risk mitigation of fruit flies in the county where this test was conducted.
Fig. 5 in A new subfamily classification of the Citrus family (Rutaceae) based on six nuclear and plastid markers
Fig. 5. Ancestral state reconstruction for the characters growth form, flower symmetry, corolla tube, and winged vs. unwinged seeds. See Fig. 2 for taxon names.
Fig. 2 in A new subfamily classification of the Citrus family (Rutaceae) based on six nuclear and plastid markers
Fig. 2. Phylogenetic reconstruction of Rutaceae. The Bayesian 50% majority-rule consensus tree based on the concatenated alignments of all six markers is shown. Posterior probability (PP) and bootstrap (BS) support values are displayed next to each branch. Strongly supported branches are marked with an asterisk (*), branches with moderate and low support in the ML analyses are represented by a degree symbol (°) and a hash key (#) respectively. A hyphen (-) indicates branches that lack statistical support.
Fig. 1 in A new subfamily classification of the Citrus family (Rutaceae) based on six nuclear and plastid markers
Fig. 1. Diversity of flowers and fruits in Rutaceae. A, Trimerous and haplostemonous flower of Cneorum tricoccon L.; B, Tetramerous and diplostemonous flower of Ruta graveolens L.; C, Pentamerous and diplostemonous flower of Philotheca verrucosa (A.Rich.) Paul G.Wilson; D, Pentamerous and polystemonous flower of Citrus trifoliata L.; E, Zygomorphic flower of Dictamnus albus L.; F, Zygomorphic flower of Ravenia spectabilis (Lindl.) Planch. ex Griseb.; G, Tubular flower with connate petals of Correa lawrenceana Hook.; H, Inconspicuous flowers with tepals of the apomictic Zanthoxylum simulans Hance; I, Pendulous, capitate inflorescence with showy bracts of Diplolaena grandiflora Desf.; J, Baccate fruit of Triphasia trifolia (Burm.f.) P.Wilson; K, Capsular fruit of Melicope clusiifolia (A.Gray) T.G.Hartley & B.C.Stone, in which seeds remain attached to the carpels; L, Capsular fruit of Dictamnus albus L., in which seeds are ejected at maturity; M, Drupaceous fruit of Acronychia brassii T.G.Hartley; N, Young winged drupes of Spathelia splendens Urb.; O, Samaroid fruit of Ptelea trifoliata L.; P, Capsular fruit of Flindersia australis R.Br. — All photos by Marc S. Appelhans, except (F) by Milton Groppo and (P) by Paul I. Forster.
Fig. 4 in A new subfamily classification of the Citrus family (Rutaceae) based on six nuclear and plastid markers
Fig. 4. Ancestral state reconstruction for the characters ovules per locule, fruit type, presence of endosperm, and chromosome number. Dashed gray lines indicate unknown character states. See Fig. 2 for taxon names.
Figures 13–18. Female genitalia. 13 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 13–18. Female genitalia. 13) C. obliquatus–sternum VIII. 14) C. obliquatus–spermatheca. 15) C. viridivittatus–sternum VIII. 16) C. viridivittatus–spermatheca. 17) C. viridivittatus–ovipositor, dorsal view. 18) C. viridivittatus–ovipositor, lateral view.
Figures 5–8. Habitus. 5 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 5–8. Habitus. 5) C. viridivittatus–male dorsal. 6) C. viridivittatus–male lateral. 7) C. viridivittatus–female dorsal. 8) C. viridivittatus–female lateral.
Figures 1–4. Habitus. 1 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 1–4. Habitus. 1) C. obliquatus–male dorsal. 2) C. obliquatus–male lateral. 3) C. obliquatus–female dorsal. 4) C. obliquatus–female lateral.
Figures 9–12. Male median Lobe. 9 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 9–12. Male median Lobe. 9) C. obliquatus–dorsal. 10) C. obliquatus –lateral. 11) C. viridivittatus–dorsal. 12) C. viridivittatus–lateral.
Figure 2 in Climatic and cultivar effects on phytoseiid species establishment and seasonal abundance on citrus
Figure 2 Abundances (number of individuals per beating sample) of phytoseiid mite species on seedlings in August. A – mean Amblyseius swirskii abundance with and without pollen provisioning. B – The relationship betweenTyphlodromus athiasae andA. swirskii abundances on different cultivars. The order of cultivars appearing in the legend corresponds to the magnitudes of their fitted intercepts (Pomello> Volka> …> Shamouti). Error bars are ± 1 SE
Figure 1 in Climatic and cultivar effects on phytoseiid species establishment and seasonal abundance on citrus
Figure 1 Phytoseiid species abundances (number of individuals per beating sample) on different cul- tivars in April, 5 weeks post release, on seedlings where Euseius stipulatus was released, with pollen provisioning (white bars), on seedlings where Euseius scutalis was released, with pollen provision- ing (gray bars), and on seedlings where no predator was released, without pollen provisioning (black bars). A – Euseius stipulatus abundances. B –Iphiseius degeneransabundances. C –Amblyseius swirskii abundances. Error bars are ± 1 SE.
Figure 3 in Climatic and cultivar effects on phytoseiid species establishment and seasonal abundance on citrus
Figure 3 Mean daily reproductive output per female (panels A and B) and survival rate (of both sexes, panels C and D), ofA. swirskii and E. stipulatus on Pomelo and Shamouti leaf discs in climate-controlled chambers. Panels A and C – Temperature regime 1 (simulating spring temperatures). Panels B and D – Temperature regime 2 (simulating summer temperatures). See Table 2 for the daily temperature schedule of each regime. Note the different scales of reproductive output between the two temperature regimes. Error bars are ± 1 SE.
Figure 1 in New mite records (Acari: Mesostigmata Trombidiformes) from soil and vegetation of some Syrian citrus agrosystems
Figure 1 Variations in the shape of dorsal body setae in the Syrian specimens ofPseudobryobia nikitensis: a – prodorsal setae; b –sc1 seta; c – c1 seta; d –d1 seta.
Figure 1 in Histopathological aspects in ripe fruits of Tahiti lime Citrus citrus x latifolia (Rutaceae) affected by phytophagous mites
Figure 1. Macroscopic and microscopic lesions on the pericarps of healthy Tahiti lime fruits affected by phytophagous mites. A–C. Healthy fruit and tissue. A. Pericarp surface; B. Pericarp surface viewed under scanning electron microscopy (SEM). Stomata can be observed; C. Cross section of the pericarp, showing the exocarp (Safranina- Alcian blue). D–F. Fruit and tissues affected by Polyphagotarsonemus latus. D. Lesions on the pericarp; E. Detail of the lesions on the pericarp surface (white arrow) (SEM); F. Cross section of the pericarp, showing the lesion affecting the exocarp and the formation of the peridermis (Safranin-Alcian blue). G–I. Fruit and tissues affected by Phyllocoptruta oleivora. G. Lesions on the pericarp; H. Detail of the lesions on the pericarp surface (white arrow) (SEM); I. Cross section of the pericarp, showing the lesion affecting the exocarp and the formation of peridermis and melanin deposits (Safranin-Alcian blue); J–L. Fruit and tissues affected by Schizotetranychus hindustanicus. J. Lesions on the pericarp. Mites nests (white arrows) can be observed; K. Mites nests in SEM (white arrow). Spider web of nest formation can be clearly seen; L. Cross section of the pericarp, showing the lesion affecting the exocarpal layers (white arrow) (Safranin-Alcian blue). CU: cuticle; EN: stomata; IEX: inner exocarp; ME: melanin; OEX:
Figure 3 in Histopathological aspects in ripe fruits of Tahiti lime Citrus citrus x latifolia (Rutaceae) affected by phytophagous mites
Figure 3. Histochemical tests applied to Tahiti lime pericarps affected by phytophagous mites (Cross sections). A–C. Pericarps affected by Polyphagotarsonemus latus, Phyllocoptruta oleivora and Schizotetranychus hindustanicus respectively. A dark brown stain can be observed due to the accumulation of polyphenols in the OEX: exocarpal layers (white arrows, Fast Blue B); D–F. Pericarps affected by Po. latus, Ph. Oleivora and S. hindustanicus respectively. A magenta stain can be observed due to the accumulation of lignin in the exocarpal layers (white arrows, Phloroglucinol acid); G–I. Pericarps affected by Po. latus, Ph. Oleivora and S. hindustanicus respectively. Callose was not detected in the exocarpal layers (Lacmoid). Melanin deposits were observed; J–L. Pericarps affected by Po. latus, Ph. Oleivora and S. hindustanicus respectively. Primary walls stain magenta and no protein or starch granules were detected (PAS-Amidoblack); M–O. Pericarps affected by Po. latus, Ph. Oleivora and S. hindustanicus respectively. Primary walls are stained purple, lignified tissues blue-green, and polyphenols brown or black (Toluidine Blue). Schizotetranychus hindustanicus lesions are restricted to feeding zones below nests (Fig. 3O) (White arrows). Peridermis formation was observed in all cases (Fig. 3A–O). CU: cuticle; IEX: inner exocarp; ME: Melanin; OEX: outer exocarp; PP: primary walls; PR: Peridermis.
Figure 2. A–E in Histopathological aspects in ripe fruits of Tahiti lime Citrus citrus x latifolia (Rutaceae) affected by phytophagous mites
Figure 2. A–E. Histochemical tests applied to healthy Tahiti lime pericarps (cross sections). A. Polyphenols Test (Fast Blue B). No positive reaction for polyphenols is observed in the exocarpal layers; B. The reaction for lignin detection (phloroglucinol acid) is negative in the exocarpal layers, but it is positive in lignified tissues (reddish staining) such as the fruit xylem (detail, white arrow); C. Callose reaction (Lacmoid) is negative in the exocarpal layers, but positive (blue staining) in fruit phloem (detail, arrow heads); D. PAS-Amidoblack test, the primary walls of the exocarpal layers and starch granules are stained magenta; E. Toluidine Blue stain, the primary walls of the exocarpal layers stain violet and cuticle dark blue. CU: cuticle; GA: starch granules; IEX: inner exocarp; OEX: outer exocarp; PP: primary walls.
MS/MS proteomics from: <em>Citrus sinensis</em> leaves in response to Diaphorina citri infestation and Huanglongbing disease
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1H NMR based metabolomics from: <em>Citrus sinensis</em> leaves in response to Diaphorina citri infestation and Huanglongbing disease
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High quality, chromosome-scale genome assemblies: Comparisons of three Diaphorina citri (Asian Citrus Psyllid) geographic populations
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Data from: The shape of aroma: Measuring and modeling citrus oil gland distribution
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.