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2,327 results for “Placement”
Fig. 5 in DNA and Morphology Corroborate the Placement of the Former New World Adoceta Bourgeois in Macrolygistopterus Pic and Updates on the Status of North American Calochrominae (Coleoptera: Lycidae)
Fig. 5. Holotype of Adoceta apicalis (female) deposited at the California Academy of Sciences. Photo credit: Rachel Diaz-Bastin/CASC Entomology (used with permission). A) Dorsal habitus, B) Ventral view, C) Lateral view, D) Frontal view with antennal details, E) Labels.
Fig. 6 in DNA and Morphology Corroborate the Placement of the Former New World Adoceta Bourgeois in Macrolygistopterus Pic and Updates on the Status of North American Calochrominae (Coleoptera: Lycidae)
Fig. 6. Holotype of Caloptognatha beameri (male) deposited at the Snow Entomological Museum Collection. A) Dorsal habitus, B) Ventral view, C) Pronotal view, D) Frontal view with antennal details, E) Male genitalia in ventral and dorsal view, respectively, F) Labels. Scale bars: 1 mm (unless otherwise noted in image).
FIGURE. 1 in Generic Placement of the Former Condaliopsis (Rhamnaceae) species
FIGURE. 1. Simultaneous-analysis strict consensus parsimonious tree with parsimony jackknife support values ≥50% above each branch and likelihood bootstrap support values ≥50% below each branch. If a support value is in brackets [], then the clade is contradicted in the likelihood analysis, and the bootstrap support for the contradictory clade with the highest support is reported.
FIGURE 1 in A multiple gene genealogy reveals the phylogenetic placement of Iodosphaeria tongrenensis sp. nov. in Iodosphaeriaceae (Xylariales)
FIGURE 1. MP tree based on dataset of LSU, ITS and SSU sequences. Bootstrap support values for maximum parsimony (MP) greater than 50% are given above the nodes. The strains numbers are given after the species names. The tree is rooted to Botryosphaeria ribis. All sequences from type strains are shown in bold face.
FIGURE 2 in A multiple gene genealogy reveals the phylogenetic placement of Iodosphaeria tongrenensis sp. nov. in Iodosphaeriaceae (Xylariales)
FIGURE 2. Iodosphaeria tongrenensis (holotype). A. Herbarium material. B, C. Ascomata on the surface of host. D. Section of ascoma. E. Peridium. F,G. Ascus apical apparatus (stained in Melzer´s reagent). H–J. Mature asci with ascospores. K. Ceratosporium -like conidia. L–O. Ascospores (N, O stained in India ink). Scale bars: B=1 mm, C=300 μm, D=50 μm, E=10 μm, F, G=5 μm, H–K=10 μm, L–O=5 μm.
FIGURE 3 in Molecular phylogeny confirms the placement of enigmatic Stachys persepolitana in Lamium (Lamiaceae; subfam. Lamioideae)
FIGURE 3. Photographs of Lamium persepolitanum. A. Lectotype, G-BOIS, B. Habit, C. Calyx, D. Corolla, E. Inflorescence of L. persepolitanum (from Yasaman Salmaki).
FIGURE 1. The 50 in Molecular phylogeny confirms the placement of enigmatic Stachys persepolitana in Lamium (Lamiaceae; subfam. Lamioideae)
FIGURE 1. The 50% majority rule consensus phylogram from a Bayesian analysis of the combined cpDNA dataset of members of subfamily Lamioideae (Lamiaceae). Posterior probabilities and non-parametric bootstrap values ≥ 50% from 1000 replicates are indicated above and below branches, respectively.
FIGURE 2. The 50 in Molecular phylogeny confirms the placement of enigmatic Stachys persepolitana in Lamium (Lamiaceae; subfam. Lamioideae)
FIGURE 2. The 50% majority rule consensus phylogram from a Bayesian analysis of the nrITS dataset of members of subfamily Lamioideae (Lamiaceae). Posterior probabilities and non-parametric bootstrap values ≥ 50% from 1000 replicates are indicated above and below branches, respectively.
FIGURE 5 in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 5. Bispora betulina, conidiophores and conidia. a. From natural wood substrate (IMI 78573, K). Scale bar = 10 μm. b. From agar plate culture (IMI 96728, K). Scale bar = 20 μm.
FIGURE 2. Corynesporopsis acaciae. a in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 2. Corynesporopsis acaciae. a. Habitat formed by stump of Acacia confusa at type locality. b. Ex-type culture on corn meal agar with red pigment diffusing from the dark brown colony.
FIGURE 4. Corynesporopsis quercicola. a, b. Conidiophores and conidia. c in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 4. Corynesporopsis quercicola. a, b. Conidiophores and conidia. c. Young conidium emerging from apical pore of the terminal conidiogenous cell. d, e. Catenate conidia. Scale bars = 20 μm.
FIGURE 1 in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 1. Maximum Likelihood tree showing estimated relationships of Corynesporopsis acaciae among Xylariales and some other orders of Sordariomycetes based on 5.8S-ITS and LSU rDNA sequences. Bootstrap values above 50% (1,000 replicates) are indicated at the nodes. The tree was rooted with the clade representing Hypocreales (Claviceps purpurea and Nectria cinnabarina).
FIGURE 3. Corynesporopsis acaciae, microscopic characteristics. a. Conidiophores and conidia from the holotype. b. Conidiophores from another, overmature specimen. c in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 3. Corynesporopsis acaciae, microscopic characteristics. a. Conidiophores and conidia from the holotype. b. Conidiophores from another, overmature specimen. c. Conidiophores from the ex-type culture shown in 2b. Scale bars: c, d, e = 10 μm.
FIGURE 3 in Phylogenetic placement and new data on macro and micro morphology of Nopalxochia phyllanthoides (Cactaceae), an endangered species from Mexico
FIGURE 3. Micro-morphological characters of Nopalxochia phyllanthoides. A) Areole with short trichomes, gloquides, base of two central spines and six radial spines, (×50). B) Apical part of a spine, continuous epidermic cells, (×900). C) Middle part of a spine, continuous epidermic cells without fissures among the cells and with smooth texture (×700). D) Glabrous epidermis, epidermic cells with smooth anticlinal walls, paracytic stomata, (×150). E) Pollen grain. F) Seed.
FIGURE 4 in Phylogenetic placement and new data on macro and micro morphology of Nopalxochia phyllanthoides (Cactaceae), an endangered species from Mexico
FIGURE 4. Phylogenetic relationships of Nopalxochia phyllanthoides. Maximum clade credibility tree for the Cactaceae family, with emphasis in PHB clade. Character support values along branches for maximum likelihood non-parametric bootstrap. Bold branches correspond with Bayesian posterior probabilities of 0.95 or above. Clade names follows Hernández-Hernández et al. (2011).
FIGURE 2 in Phylogenetic placement and new data on macro and micro morphology of Nopalxochia phyllanthoides (Cactaceae), an endangered species from Mexico
FIGURE 2. Morphological floral characters of Nopalxochia phyllanthoides. A) Longitudinal flower view, whitish filaments and yellow anthers, very long style, thin and white, yellow stigma lobes. B) Interior tepal finishing in a dark mucro. C) Seven stigma lobes, yellowish and papillate. D) Yellow anthers with longitudinal dehiscence. E) Pericarpel showing scales with the a dark and widen base. F) Ovaric chamber showing numerous white ovules.
FIGURE 1 in Phylogenetic placement and new data on macro and micro morphology of Nopalxochia phyllanthoides (Cactaceae), an endangered species from Mexico
FIGURE 1. Habitat and macro morphology of Nopalxochia phyllanthoides. A) Epiphyte wild plant growing on Ostrya virginiana (Miller 1768: without pagination) Koch (1873: 6–7), 1.13 m tall, B) Ramified phylloclades, showing the flower base bend upwards. C) Flower in anthesis, internal segments pink, superior view. Recollected in the Municipality of Tenango de Doria, Hidalgo.
FIGURES 108–113 in The diatom genus Oricymba in Vietnam and Laos with description of one new species, and a consideration of its systematic placement
FIGURES 108–113. Oricymba voronkinae sp. nov. 108. external view. 109–113, internal views. 108. Girdle view showing distinct marginal ridge and striae extending from valve face to mantle. 109. Low magnification valve view with distinct central nodule present. 110, 111. Central area demonstrating lack of an intermission and two elongate-elliptical stigma openings occluded by a dendritic structure. 112, 113. Apices with distinct helictoglossae offset from axial area. Siliceous granules are present around aveoli. Porelli area restricted to the mantle. Scale bars = 5 μm in Fig. 108; 10 μm in Fig. 109; 1 μm in Figs 110, 112; 0.5 μm in Figs 111, 113.
FIGURES 74–101 in The diatom genus Oricymba in Vietnam and Laos with description of one new species, and a consideration of its systematic placement
FIGURES 74–101. Oricymba voronkinae sp. nov. LM. Valve views showing size range. Holotype is illustrated in Fig. 75. Scale bar = 10 μm.
FIGURES 70–73 in The diatom genus Oricymba in Vietnam and Laos with description of one new species, and a consideration of its systematic placement
FIGURES 70–73. Oricymba perjaponica, comb. nov. SEM, external views. 70. Low magnification valve view. The arched raphe and stigma opening are evident. 71. Central area showing dilated proximal raphe ends and round stigma opening. Rectangular striae with subtending dendritic coverings are evident. 72. Axial area showing striae structure and presence of marginal ridges. 73. Apex with pore field porelli physically separate and structurally differentiated from areolae. The distal raphe end does not bisect the pore field. Scale bars = 10 μm in Fig. 70, 1 μm in Figs 71, 72 and 0.5 μm in Fig. 73.
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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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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.