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684 results for “Phylogenetic placement”
FIGURE 5 in First record of Larsonella pumilus (Teleostei: Gobiidae) from Japan, with phylogenetic placement of the genus Larsonella
FIGURE 5. Underwater photograph (A) and a dried shell (B and C) of Xenophora chinensis. A, Collecting the shell in which Larsonella pumilus may have taken refuge, using a Remotely Operated Vehicle at a depth of 214 m in the East China Sea off Seragaki, Onna Village, Okinawa, Japan. B (dorsal view) and C (ventral view) are likely the same shell as A. Scale bars, 10 mm.
FIGURE 2 in First record of Larsonella pumilus (Teleostei: Gobiidae) from Japan, with phylogenetic placement of the genus Larsonella
FIGURE 2. Three-dimensional images of the head of Larsonella pumilus reconstructed from microcomputed tomography data. A, frontal view, showing the outermost teeth. B, mid-sagittal view of the right side (cut along section x-x' in A), showing inner teeth without a part of ceratohyal and 5th branchiostegal ray to observe teeth easily. Red, premaxilla and outermost teeth on the premaxilla; blue, dentary and outermost teeth on the dentary. Triangles, vestiges of missing teeth. Scale bars, 1 mm.
FIGURE 2. Mimosa pabstiana. A in Phylogenetic placement of Mimosa pabstiana reinforces a biogeographic pattern of the Pleistocene Arc Theory in Mimosa (Leguminosae, Caesalpinoideae)
FIGURE 2. Mimosa pabstiana. A. Detail of flowering branches. B. Detail of flowering and fruiting branches. C. Detail of craspedia. (photographed by A.C. Sevilha).
FIGURE 4. Mimosa paraibana. A in Phylogenetic placement of Mimosa pabstiana reinforces a biogeographic pattern of the Pleistocene Arc Theory in Mimosa (Leguminosae, Caesalpinoideae)
FIGURE 4. Mimosa paraibana. A. Detail of capitate inflorescences. B. Detail of craspedia. C. Detail of habit. D. Detail of spicate, paniculate inflorescences (A and C, photographed by Leonardo Jales Leitão; B, photographed by Dr. Rubens Queiroz; D, photographed by M.F. Simon).
FIGURE 1 in Phylogenetic placement of Mimosa pabstiana reinforces a biogeographic pattern of the Pleistocene Arc Theory in Mimosa (Leguminosae, Caesalpinoideae)
FIGURE 1. Phylogeny of Mimosa based on DNA sequences of the trnD-trnT noncoding plastid locus. The 50% majority-rule consensus tree from a Bayesian analysis. Letters on nodes represent well-supported clades recognized by Simon et al. (2011). Numbers next to nodes are posterior probabilities. The lines in gray represent trimerous lineages.
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 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.
FIGURE 6 in Lapidia, a new monotypic genus of Asteraceae (Eupatorieae) from Brazil, and its phylogenetic placement
FIGURE 6. Genera of Eupatorieae sympatric with Lapidia (Clade Z) in the Chapada Diamantina, Bahia state. A–B. Semiria viscosa D.J.N.Hind. A. Habit. B. Detail of head, showing convex, epaleaceous receptacle, and epappose cypselae. C. Stylotrichium glomeratum Bautista et al. D. Stylotrichium sucrei R.M.King & H.Rob. (Photographs: A–C: V.Amorim; D: S.C.Ferreira).
FIGURE 4 in Lapidia, a new monotypic genus of Asteraceae (Eupatorieae) from Brazil, and its phylogenetic placement
FIGURE 4. Endemic genera of Eupatorieae in the Chapada Diamantina, Bahia state (Clade W). A–B. Bahianthus viscosus R.M.King & H.Rob. A. Fruits in dispersal. B. Flowers in anthesis. C. Catolesia huperzioides Roque et al. Flowering branch with dense spiral of leaves. D–E. Morithamnus crassus R.M.King & H.Rob. D. Habit. E. Buds and flowers in anthesis. (Photographs: A–B: L.Moura; C. A.A.Conceição; D–E: N.Roque).
FIGURE 3. Majority-rule 50 in Lapidia, a new monotypic genus of Asteraceae (Eupatorieae) from Brazil, and its phylogenetic placement
FIGURE 3. Majority-rule 50% consensus tree of a Bayesian analysis to study the phylogenetic placement of Lapidia apicifolia among selected taxa of the "CAFE clade" (according to Rivera et al. 2016a) (Eupatorieae, Asteraceae), based on a combined matrix with sequence data from the internal transcribed spacer (ITS1 and ITS2) of the nuclear ribosomal DNA and the trnL–trnF plastid region (trnL intron, trnL-trnF spacer). Branch colors follow the same color scheme of Rivera et al. (2016a), and the values above branches correspond to the posterior probabilities calculated from the 18,000 trees obtained in the analysis after excluding burn-in.
FIGURE 5 in Lapidia, a new monotypic genus of Asteraceae (Eupatorieae) from Brazil, and its phylogenetic placement
FIGURE 5. Genera of Eupatorieae sympatric with Lapidia (Clade Z) in the Chapada Diamantina, Bahia state. A. Agrianthus myrtoides Mattf. B. Agrianthus giulietiae D.J.N.Hind. C. Arrojadocharis santosii R.M.King & H.Rob. D–E. Lasiolaena blanchetii (Sch.Bip. ex Baker) R.M.King & H.Rob. F. Lasiolaena duartei R.M.King & H.Rob.: bicolored leaves. (Photographs: A: N.Roque; B: L.Moura; C–F: V.Amorim).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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