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384 results for “epiphyte”
Data from: Genetic inference of epiphytic orchid colonization; it may only take one
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Data from: Biodiversity in agricultural landscapes: the effect of apple cultivar on epiphyte diversity
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Community structure of vascular epiphytes: a neutral perspective
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Epiphytic diatom community structure and richness is determined by macroalgal host and location in the South Shetland Islands (Antarctica)
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Making the most of your pollinators: An epiphytic fig tree encourages its pollinators to roam between figs
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Data from: Consequences of swamp forest fragmentation on assemblages of vascular epiphytes and climbing plants: evaluation of the metacommunity structure
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The mycorrhizal community of the epiphytic orchid Thrixspermum japonicum is strongly biased toward a single Ceratobasidiaceae fungus, despite a wide range of fungal partners
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Data from: Trait patterns of epiphytes compared to other plant life forms along a tropical elevation gradient
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Data on epiphytic lichens along elevational gradients in South Tyrol, Italy
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Data from: Structure of the epiphyte community in a tropical montane forest in SW China
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Data from: European phylogeography of the epiphytic lichen fungus Lobaria pulmonaria and its green algal symbiont
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Sustainable harvesting and conservation of Laelia furfuracea, a rare epiphytic orchid from Oaxaca, Mexico
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Data from: Extensive yellow crusts below limestone overhangs: a new taxon close to a minute epiphytic lichen
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Data from: Tropical forest restoration enriches vascular epiphyte recovery
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Fig. 6 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 6. Neophyllobius tescalicola sp. nov., ♀, holotype. A. Palp. B. Subcapitulum. C. Dorsal idiosoma. D. Ventral idiosoma. E. Trochanter–tibia of leg I. F. Tarsus I.
Fig. 3 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 3. Schematic leg setations of Neophyllobius cibyci sp. nov. A–D. ♀, holotype. A. Trochanter–tibia of leg I. B. Trochanter–tibia of leg II. C. Trochanter–tibia of leg III. D. Trochanter–tibia of leg IV. E–H. ♁, paratype (CNAC009238). E. Trochanter–tibia of leg I. F. Trochanter–tibia of leg II. G. Trochanter–tibia of leg III. H.Trochanter–tibia of leg IV. I–L. Protonymph, paratype (CNAC009241). I. Trochantertibia of leg I. J. Trochanter–tibia of leg II. K. Trochanter–tibia of leg III. L. Trochanter–tibia of leg IV. M–O. Larva, paratype (CNAC009242). M. Trochanter–tibia of leg I. N. Trochanter–tibia of leg II. O. Trochanter–tibia of leg III.
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>
Data from: Effects of forest-use intensity on vascular epiphyte diversity along an elevational gradient
Aim: Understanding patterns of tropical plant diversity and their vulnerability to anthropogenic disturbance at different spatial scales remains a great challenge in ecology and conservation. Here, we study how the effects of forest-use intensity on vascular epiphyte diversity vary along a tropical elevational gradient. Location: 3500-m elevational gradient along the eastern slopes of Cofre de Perote, Mexico. Methods: We studied the effects of forest-use intensity on alpha, beta, and gamma diversity of vascular epiphyte assemblages in old-growth, degraded, and secondary forests at eight study sites at 500 m intervals along the elevational gradient. At each elevation and in each of the three forest-use intensity levels, we established five 400 m² plots yielding a total of 120 plots. Results: Interactive effects of elevation and forest-use intensity strongly impacted local-scale patterns of vascular epiphyte diversity. We found a bimodal trend, with species diversity peaking at 500 and 1500 m above sea-level, which deviates from the previously reported humped-shaped pattern. In most cases alpha diversity did not differ significantly among forest-use intensity levels. However, gamma diversity was always lower in secondary forests compared to old-growth forests across the entire elevational gradient. Within each elevational belt, beta diversity was dominated by species turnover along the forest-use intensity gradient in the lowlands and declined with increasing elevation, where community composition became increasingly nested. Along the elevational gradient, the spatial turnover of vascular epiphyte community composition was similar among forest-use intensity levels. Main conclusions: Our results reveal a strong interaction between forest-use intensity and elevation, making it difficult to extrapolate findings from one elevational belt to another. Our findings highlight the value of old-growth forest for epiphyte diversity, but also show that degraded and secondary forests –depending on the elevational belt– may maintain a high species diversity, and thus play an important role in conservation planning.
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.
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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
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.