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403 results for “morphological characteristics”
FIGURE 5 in Tuberculina photiniae sp. nov. (Helicobasidiales, Basidiomycota) supported by morphological characteristics and phylogenetic data
FIGURE 5. Conidiophores, phialide and conidia of Tuberculina photiniae. a, b Conidiophores. c Conidiogenous cells and conidia on their tops. d Conidia. Bars: a–d = 10 μm.
FIGURE 4 in Tuberculina photiniae sp. nov. (Helicobasidiales, Basidiomycota) supported by morphological characteristics and phylogenetic data
FIGURE 4. The sections of the sporodochia of Tuberculina photiniae and the aecia of the rust. (A, B) The sporodochia on the aecia. (C) Sporodochia. (D) Aecia of Aecidium wenshanese. Bars: A, C, D = 100 μm; B = 200 μm.
FIGURE 3 in Heterobasidion amyloideopsis sp. nov. (Basidiomycota, Russulales) evidenced by morphological characteristics and phylogenetic analysis
FIGURE 3. Chronogram and estimated divergence times of Heterobasidion spp. generated from molecular clock analysis using the RPB1-RPB2 data. Chronogram obtained using the Heterobasidion divergence time of 19.72 Mya (Chen et al. 2015) as the calibration point is shown. The calibration point and objects of this study are marked in the chronogram. The geological time scale is in millions of years ago (Mya). Divergence times of H. amyloideopsis highlighted in bold.
FIGURE 5 in Heterobasidion amyloideopsis sp. nov. (Basidiomycota, Russulales) evidenced by morphological characteristics and phylogenetic analysis
FIGURE 5. Microscopic structures of Heterobasidion amyloideopsis (drawn from the holotype). a. basidiospores. b. basidia and basidioles. c. cystidioles. d. hyphae from trama. e. hyphae from context. Bars: a–5 μm; b–e–10 μm.
FIGURE 2 in Tuberculina photiniae sp. nov. (Helicobasidiales, Basidiomycota) supported by morphological characteristics and phylogenetic data
FIGURE 2. Maximum Parsimony strict consensus tree illustrating the phylogeny of Tuberculina photiniae and related species based on the combined ITS+nLSU sequence datasets. Branches are labelled with maximum likelihood bootstraps higher than 70%, parsimony bootstrap proportions higher than 50% and Bayesian posterior probabilities greater than 0.95. Clade names follow Lutz et al. (2004b).
FIGURE 2 in Heterobasidion amyloideopsis sp. nov. (Basidiomycota, Russulales) evidenced by morphological characteristics and phylogenetic analysis
FIGURE 2. Maximum Parsimony strict consensus tree illustrating the position of Heterobasidion amyloideopsis and related species in the H. insulare complex based on the combined ITS+LSU+RPB1+RPB2 sequences. Branches are labeled with maximum likelihood bootstrap higher than 70%, parsimony bootstrap proportions higher than 50% and Bayesian posterior probabilities more than 0.95 respectively.
FIGURE 1 in Heterobasidion amyloideopsis sp. nov. (Basidiomycota, Russulales) evidenced by morphological characteristics and phylogenetic analysis
FIGURE 1. Maximum Parsimony strict consensus tree illustrating the position of Heterobasidion amyloideopsis and related species based on the combined RPB1+RPB2 sequences. Branches are labeled with maximum likelihood bootstrap higher than 70%, parsimony bootstrap proportions higher than 50% and Bayesian posterior probabilities more than 0.95 respectively.
FIGURE 3 in Morphological characteristics and molecular data reveal two new species of Dentipellis from China
FIGURE 3. Strict consensus tree illustrating the phylogeny of Dentipellis by Maximum Parsimony based on ITS and nLSU sequences. Parsimony bootstrap values (before the slash markers) higher than 50% and Bayesian posterior probabilities (after the slash markers) more than 0.95 were indicated along branches.
FIGURE 2 in Morphological characteristics and molecular data reveal two new species of Dentipellis from China
FIGURE 2. Dentipellis tropicalis (holotype). a. Basidiospores. b. A vertical section through a spine. c. Hyphae from subiculum.
FIGURE 1 in Morphological characteristics and molecular data reveal two new species of Dentipellis from China
FIGURE 1. Dentipellis longiuscula (holotype). a. Basidiospores. b. A vertical section through a spine. c. Hyphae from subiculum.
Table ̚: Diagnostic morphological characteristics of the Hipposideros armiger captured in cave of the Sadar Upazila subdistrict (Bandarban district, Bangladesh) and closely related species of the genus Hipposideros in South Asia according to Srinivasulu et al. (2010). in First record of Great Himalayan leaf-nosed bat, Hipposideros armiger (Hipposideridae) from Bangladesh
<p><b>Table ̚:</b> Diagnostic morphological characteristics of the <i>Hipposideros armiger</i> captured in cave of the Sadar Upazila subdistrict (Bandarban district, Bangladesh) and closely related species of the genus <i>Hipposideros</i> in South Asia according to Srinivasulu et al. (2010).</p><table><tbody><tr><th><b>External characters</b></th><th><b>This study</b></th><th><i>H. armiger</i></th><th><i>H. speoris</i></th><th><i>H. larvatus</i></th><th><i>H. lankadiva</i></th></tr></tbody><tbody><tr><th><b>(mm)</b></th><td></td><td><b>(Hodgson, ̚s̒ƽ)</b></td><td><b>(Schneider, ̚see)</b></td><td><b>(Horsfield, ̚sz̒)</b></td><td><b>(Kellart, ̚sƽe)</b></td></tr><tr><th>Forearm length</th><td>90.1</td><td>85.4–95.0</td><td>45.6–54.0</td><td>61.2–64.8</td><td>75.0–99.0</td></tr><tr><th>Head body length</th><td>98.3</td><td>82.0–105.0</td><td>46.0–62.0</td><td>74.0–78.0</td><td>87.0–106.0</td></tr><tr><th>Tail length</th><td>49.9</td><td>50.0–64.0</td><td>20.0–29.0</td><td>37.0–44.0</td><td>35.0–58.0</td></tr><tr><th>Ear length</th><td>26.6</td><td>26.0–34.0</td><td>12.5–19.0</td><td>23.0–26.0</td><td>19.5–30.0</td></tr><tr><th>No. of supplementary</th><td>4 (4th much</td><td>4 (4th much reduced)</td><td>3 (3rd much reduced)</td><td>4 (4th much reduced)</td><td>4 (4th sometimes</td></tr><tr><th>leaflets</th><td>reduced)</td><td></td><td></td><td></td><td>absent)</td></tr></tbody></table>
FIGURE 45 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 45. Arrenurus inexploratus: A—ventral side, B—dorsal plate, C—excretory pore plate, D—pedipalp (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 42 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 42. Arrenurus biscissus: A—ventral side, B—dorsal plate, C—excretory pore plate, D—pedipalp (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 39 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 39. Arrenurus truncatellus: A—ventral side, B – dorsal plate, C – excretory pore plate, D—leg I (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 37 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 37. Arrenurus nodosus: A—ventral side, B – dorsal plate, C – excretory pore plate, D – pedipalp, E – leg I (scale bars: A, B—100 µm; C, D, E—20 µm).
FIGURE 48 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 48. Arrenurus pugionifer: A—ventral side, B—dorsal plate, C—excretory pore plate, D—pedipalp (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 36 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 36. Arrenurus knauthei: A—ventral side, B—dorsal plate, C—excretory pore plate, D—pedipalp (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 35 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 35. Arrenurus conicus: A—ventral side, B—dorsal plate, C—excretory pore plate, D—leg III (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 34 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 34. Arrenurus cylindratus: A – ventral side, B—dorsal plate, C—excretory pore plate, D—leg I (scale bars: A, B—100 µm; C, D—20 µm).
FIGURE 32 in Morphological characteristics of water mite larvae of the genus Arrenurus Dugès, 1834, with notes on the phylogeny of the genus and an identification key
FIGURE 32. Arrenurus stjoerdalensis: A—ventral side, B – dorsal plate, C – excretory pore plate, D – leg III (scale bars: A, B—100 µm; C, D—20 µm).
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.