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96 results for “epiphytic species”
FIGURE 1. Cymbidium lii. M.Z.Huang, J.M.Yin & G.S in An unusual new epiphytic species of Cymbidium (Orchidaceae: Epidedroideae) from Hainan, China
FIGURE 1. Cymbidium lii. M.Z.Huang, J.M.Yin & G.S.Yang, sp. nov. A. Habit. B. Flowers. Photograph by Ming-Zhong Huang.
FIGURE2. Colletotrichum serranegrense COAD 2100. A in Colletorichum serranegrense sp. nov., a new endophytic species from the roots of the endangered Brazilian epiphytic orchid Cattleya jongheana
FIGURE2. Colletotrichum serranegrense COAD 2100. A, Setae; B, Appressoria; C, Conidiophores; D, Conidia. Scale bars =10 μm.
FIGURE 3 in Colletorichum serranegrense sp. nov., a new endophytic species from the roots of the endangered Brazilian epiphytic orchid Cattleya jongheana
FIGURE 3. Bayesian phylogenetic tree inferred from DNA sequence data from multigene alignment (ITS, ACT, TUB2, CHS-1). Bayesian posterior probabilities (BPP,> 0.50) and RAxML bootstrap support (MLBS,> 50) values are indicated at the nodes (BPP/MLBS). The type status of strains is indicated with an asterisk (*) and specimens representing the new species are in bold face. The tree was rooted with Colletotrichum gloeosporioides (isolate CBS 953.97).
FIGURE 1 in Verrucaria tenebrosa (Verrucariaceae), a new lichen species from Finland and Norway, and notes on the taxonomy of epiphytic taxa belonging to the V. hydrophila complex
FIGURE 1. Phylogenetic relationships of Verrucaria tenebrosa and related species. A maximum likelihood phylogram obtained from RAxML analysis based on ITS data set. Bootstrap values (>50%) are shown at nodes. New species described in this study are indicated in bold.
FIGURE 2 in Clistax bahiensis (Acanthaceae), a new epiphytic species from Bahia, Brazil
FIGURE 2. Clistax bahiensis Profice & Leitman at Serra das Lontras National Park, Arataca, Bahia. A. Flowering branch. B. Bracts, bracteoles and corolla.
FIGURE 1. Clistax bahiensis Profice & Leitman. A. Branch. B. Inflorescence. C in Clistax bahiensis (Acanthaceae), a new epiphytic species from Bahia, Brazil
FIGURE 1. Clistax bahiensis Profice & Leitman. A. Branch. B. Inflorescence. C. Detail of flowering branches. D. Bracts, bracteoles and corolla. E. Posterior bracteole. F. Anterior bracteole. G. Corolla. H. Anthers. I. Upper portion of style showing stigma unequal. J. Capsule front view. K. Capsule lateral view. L. Detail of the fruit with persistent calyx and disc (W.W.Thomas et al. 14205).
FIGURE 3 in Clistax bahiensis (Acanthaceae), a new epiphytic species from Bahia, Brazil
FIGURE 3. Scanning electron (SEM) photomicrographs of Clistax pollen A. C. speciosus Nees equatorial view. B. C. brasiliensis Mart. equatorial view. C. C. bahiensis Profice & Leitman equatorial view. D. C. bahiensis Profice & Leitman detail of pollen surface
FIGURE. Map of Mexico, indicating the number of families, genera, and species of Mexican Vascular Epiphytes by state. in Mexican Vascular Epiphytes: Richness and Distribution
FIGURE. Map of Mexico, indicating the number of families, genera, and species of Mexican Vascular Epiphytes by state.
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano. in The genus Ramalina Acharius (Ascomycota, Lecanoromycetes, Ramalinaceae) in northern South America
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano.
FIGURE 3 in Gastrochilus pseudocalceolaris, a new species of epiphytic orchid from India
FIGURE 3. Labellum of – A, B. Gastrochilus calceolaris (Buch.-Ham. ex Sm.) D. Don; C. G. acaulis (Lindl.) Kuntze; D, E. G. pseudocalceolaris S. Dey, L. Phom, Av. Bhattacharjee, Moaakum & K. Eshuo.
FIGURE 2. Gastrochilus pseudocalceolaris S. Dey, L in Gastrochilus pseudocalceolaris, a new species of epiphytic orchid from India
FIGURE 2. Gastrochilus pseudocalceolaris S. Dey, L. Phom, Av. Bhattacharjee, Moaakum & K. Eshuo. A. Habit; B. Flower; C. Portion of inflorescence; D. Dorsal sepal; E. Petal; F. Lateral sepal; G. Labellum, column and pedicel plus ovary; H. Labellum with portion of column and pollinarium; I. Flower; J. Labellum, column and pedicel plus ovary; K. Labellum; L. Pollinarium; M. Dehisced capsule showing seeds. [From S. Dey 1342 (Holotype and isotype); I–M: From preserved flowers taken from S. Dey 1342 before mounting]
FIGURE 1. Gastrochilus pseudocalceolaris S. Dey, L in Gastrochilus pseudocalceolaris, a new species of epiphytic orchid from India
FIGURE 1. Gastrochilus pseudocalceolaris S. Dey, L. Phom, Av. Bhattacharjee, Moaakum & K. Eshuo. A–B. Photograph of plant in natural habitat; C. Habit.
FIGURE 2 in Phylogenetics of two rhizomatous epiphytic species of Cymbidium (Orchidaceae; Cymbidieae): evidence from analyses of nuclear and plastid DNA
FIGURE 2. Maximum likelihood tree for Cymbidium based on combined nuclear and plastid DNA regions. The previously recognised sections from Liu et al. (2006) are highlighted by the colour of branches. Numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BS ML, BS MP, PP). A dash (–) indicates that the node is inconsistent between the topology of the MP/ML trees and the Bayesian tree. "*" indicates that the node has 100 bootstrap percentage or 1.00 posterior probability.
FIGURE 1 in Phylogenetics of two rhizomatous epiphytic species of Cymbidium (Orchidaceae; Cymbidieae): evidence from analyses of nuclear and plastid DNA
FIGURE 1. Phylogenetic comparison between the ML/MP/BI trees of Cymbidium based on nuclear ribosomal ITS (left) and plastid DNA (right). Numbers near the nodes are bootstrap percentages and Bayesian posterior probabilities (BS, BS, PP). A dash (–) indicates that ML MP the node is inconsistent between the topology of the MP/ML trees and the Bayesian tree. "*" indicates that the node has 100 bootstrap percentage or 1.00 posterior probability.
Data from: Primary ecological succession in vascular epiphytes: the species accumulation model
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Data from: Environmental optimality, not heterogeneity, drives regional and local species richness in lichen epiphytes
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Species richness and abundance of vascular epiphytes along an elevation gradient
<p>Because of the difficulty in sampling and the logistics of identifying canopy-dwelling plants, the number of inventories quantifying tropical epiphytes is limited. This has resulted in a substantial gap in knowledge, even though forest canopies contain significant biodiversity and forest biomass. In the case of Volcán Maderas, multiple ecological and taxonomic research initiatives have been conducted. However, for vascular epiphytes, georeferenced specific spatial descriptions were lacking and a standardized effort for documenting species richness was non-existent. We provide a detailed qualitative and quantitative assessment of the vascular epiphyte flora and its spatial distribution. These data shed light on important plant assemblages across elevational gradients that can be used for monitoring and understanding adaptive strategies to drought conditions.</p>
Figure 2 from: Francisco-Gutiérrez A, Cházaro-Basáñez M, Carral-Domínguez R (2023) The first epiphytic species of Valeriana in the world: Valeriana rudychazaroi (Caprifoliaceae). PhytoKeys 236: 145-156. https://doi.org/10.3897/phytokeys.236.110905
Figure 2 Valeriana rudychazaroi on Quercus glabrescens trees in the field. Photograph taken by Rodrigo Carral-Domínguez.
Figure 3 from: Francisco-Gutiérrez A, Cházaro-Basáñez M, Carral-Domínguez R (2023) The first epiphytic species of Valeriana in the world: Valeriana rudychazaroi (Caprifoliaceae). PhytoKeys 236: 145-156. https://doi.org/10.3897/phytokeys.236.110905
Figure 3 Valeriana rudychazaroi in the field. A habitat at an altitude of 3–6 m on Quercus glabrescens trees B detail of inflorescence with flowers and fruit C hosts in cloud forests from central Veracruz, Mexico. Photographs taken by Rodrigo Carral-Domínguez.
Figure 1 from: Francisco-Gutiérrez A, Cházaro-Basáñez M, Carral-Domínguez R (2023) The first epiphytic species of Valeriana in the world: Valeriana rudychazaroi (Caprifoliaceae). PhytoKeys 236: 145-156. https://doi.org/10.3897/phytokeys.236.110905
Figure 1 Valeriana rudychazaroi Cházaro, Franc.Gut. & J.R.Carral. A habit of flowering branch B staminate flower C fruit. Drawn from the holotype Carral-Domínguez & Cházaro-Basáñez 766 (XAL). Illustration by Gerardo Andrade–Quintos.
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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.
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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.