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1,968 results for “morphological taxonomy”
FIGURES 47–54 in Taxonomy of ' Euconnus complex'. Part III. Morphology of Euconnus subgenus Napochus and revision of the Australian species (Coleoptera, Staphylinidae, Scydmaeninae)
FIGURES 47–54. Napochus of Australia; aedeagus in ventral (47, 49, 51, 53) and lateral (48, 50, 52, 54) views. Euconnus feeneyi feeneyi sp. n. (47–50), E. feeneyi parallelilaminatus ssp. n. (51–54).
FIGURES 1–2 in Taxonomy of ' Euconnus complex'. Part III. Morphology of Euconnus subgenus Napochus and revision of the Australian species (Coleoptera, Staphylinidae, Scydmaeninae)
FIGURES 1–2. General morphology of Euconnus (Napochus) claviger (Müller & Kunze), the type species of Napochus, in dorsal (1) and lateral (2) views.
FIGURES 24–34 in Taxonomy of ' Euconnus complex'. Part III. Morphology of Euconnus subgenus Napochus and revision of the Australian species (Coleoptera, Staphylinidae, Scydmaeninae)
FIGURES 24–34. Napochus of Australia; dorsal habitus (24–25, 28–34) and original labels of holotypes (26–27). Euconnus palmwoodianus (Franz) (24, 26), E. pisoniae Franz (25, 27), E. setiphallus sp. n. (28), E. yadhaigana sp. n. (29), E. microlaminatus sp. n. (30), E. feeneyi feeneyi sp. n. (31, 32), E. feeneyi parallelilaminatus ssp. n. (33, 34).
FIGURES 11–13 in Taxonomy of ' Euconnus complex'. Part III. Morphology of Euconnus subgenus Napochus and revision of the Australian species (Coleoptera, Staphylinidae, Scydmaeninae)
FIGURES 11–13. Details of morphology of Euconnus (Napochus) claviger (Müller & Kunze). Pterothorax and abdomen in ventral view (11), mesothorax in ventral view (12), posteromedian part of metathorax and base of abdomen in ventral view (13). Abbreviations: anterior ridge; cx3, metacoxa; epm3, metepimeron; mscc, mesocoxal cavity; mscs, mesocoxal socket; mcp, mesocoxal projection; msff, mesofurcal fovea; msvp, mesoventral intercoxal process; mtvp, metaventral intercoxal process; pcr, procoxal rest; pre, prepectus; tr3, metatrochanter; v3, metaventrite.
FIGURES 10–13 in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURES 10–13. Scanning electron microscopy of a specimen of Phyllodistomum wallacei n. sp. 10. Adult, ventral view, with scattered dome-like papillae on hind- and forebody. 11. Oral sucker, showing 7 pairs of papillae. 12. Ventral sucker, showing 3 pairs of papillae. 13. Dome-like papillae with small projections.
FIGURE 14 in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURE 14. Coalescent-based phylogenetic tree obtained from the species tree analysis of the combined data set (COI+28S). The scale bar represents the number of nucleotide substitutions per site. Filled circles above/below branches represent Bayesian posterior probability ≥ 0.95. GenBank accession numbers of the new species are given in the taxonomic remarks section.
FIGURES 6–9 in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURES 6–9. Scanning electron microscopy of a specimen of Phyllodistomum cribbi n. sp. 6. Adult, ventral view. 7. Oral sucker, showing 4 pairs of papillae. 8. Ventral sucker, showing 3 pairs of papillae. 9. Ventral surface of hindbody exhibiting papillae on the tegument.
FIGURES 2–5 in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURES 2–5. Line drawings of the holotype of P. cribbi n. sp. and P. wallacei n. sp., and detail of the male reproductive system of both species 2. Phyllodistomum cribbi n. sp. from Zoogoneticus quitzeoensis, ventral view. 3. Detail of the cirrus sac of P. cribbi n. sp. 4. Phyllodistomum wallacei n. sp. from Ilyodon furcidens, ventral view. 5. Detail of the cirrus sac of P. wallacei n. sp. Symbols: os = oral sucker, gp = genital pore, c = cecum, vs = ventral sucker, vg = vitelline gland, o = ovary, t = testis, e = eggs.
FIGURE 1. Hydrological systems and collection sites for Phyllodistomum cribbi n in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURE 1. Hydrological systems and collection sites for Phyllodistomum cribbi n. sp. (square) and P. wallacei n. sp. (circles) in central Mexico. Full green circles and square correspond to localities where specimens were collected for molecular phylogenetic analyses; full grey circle and square indicate specimens identified either as Dendrorchis sp. or Phyllodistomum sp. from previous studies. These records were not included in the phylogenetic analyses in this study.
FIGURE 4. A in Unraveling Tragia peltata (Euphorbiaceae): taxonomy, morphology, distribution and conservation
FIGURE 4. A. Geographic distribution of Tragia peltata in the Atlantic Forest in the states of Bahia (BA), Espírito Santo (ES), and Rio de Janeiro (RJ), Brazil. B. Spatial distribution of the Phytophisiognomies in the area of occurrence of T. peltata, stats of Bahia (BA), Espírito Santo (ES), Minas Gerais (MG), and Rio de Janeiro (RJ).
FIGURE 3 in Unraveling Tragia peltata (Euphorbiaceae): taxonomy, morphology, distribution and conservation
FIGURE 3. Leaf variability in Tragia peltata. Population from Rio de Janeiro state. A. Leaf blade, B. Leaf base on adaxial view, C. Leaf margin. Population from Bahia and Espírito Santo states. D. Leaf blade, E. Base of leaf blade with petiole insertion close to the margin, F. Leaf margin. A‒C from D. Sucre & J. Gomes 11277 (RB); D‒F from T.S. Santos 1551 (CEPEC). Scale = 1 cm (A‒B and D‒E) or 0.1 cm (C and F).
FIGURE 1 in Unraveling Tragia peltata (Euphorbiaceae): taxonomy, morphology, distribution and conservation
FIGURE 1. Lectotype of Tragia peltata. Original plate of T. peltata (1831b) on Flora Fluminensis in the Manuscripts Section of the National Library of Rio de Janeiro (cat. no.: mss1198659_010).
Supplementary material 1 from: Prasad D, Kumar R, Jaiswal S, Yadav R, Tiwari S, Agnihotri P (2022) An update on the taxonomy of Calamagrostis nagarum (Bor) G.Singh and its allies (Poaceae, Agrostidinae): morphometrics and micro-morphology. PhytoKeys 212: 135-155. https://doi.org/10.3897/phytokeys.212.89253
Quantitative data of morphological characters and elevation data of Calamagrostis lahulensis, C. nagarum, and C. scabrescens
FIGURE 1 in Taxonomy and morphology of Phacidiella kunmingensis sp. nov. (Stictidaceae) from southwest China
FIGURE 1. RAxML tree inferred from combined ITS, LSU, mtSSU and rpb2 sequence. Bootstrap support for maximum likelihood analysis equal to or greater than 70% and Bayesian posterior probabilities equal to or above 0.95 are denoted next to the notes in this order. The newly introduced species are marked in blue and the type strains are indicated in black bold font.
FIGURE 2 in Taxonomy and morphology of Phacidiella kunmingensis sp. nov. (Stictidaceae) from southwest China
FIGURE 2. Phacidiella kunmingensis (HKAS 124175, holotype). a Substrate. b, c Apothecia. d, e Vertical section of apothecia. f Subhymenium. g Exciplum. h Hymenium. i–k Paraphyses showing faintly blue iodine reaction. l–n Asci. o–q Ascospores. r Ascus cap. s, t Upper and lower view of culture on PDA after 48 days. Scale bars: d = 500 µm, e = 200 µm, g, h = 100 µm, l–p = 50 µm, f = 30 µm, i–k, q, r = 10 µm. (i–n, r were treated with Melzer's reagent)
Figure 4 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 4. Sonograms of territorial songs of Lyncornis. A, Lyncornis macrotis bourdilloni, Kerala, India, B. King. B, Lyncornis macrotis cerviniceps, Thailand, J. C. Roché (BLSA 42510). C, Lyncornis macrotis jacobsoni, Simeulue Island, F. Verbelen. D, Lyncornis temminckii, Johore, Malaysia, T. C. White (BLSA 6414). E, L. temminckii, Way Kambas, Sumatra, A. B. van den Berg (ML 70527). F, Lyncornis macrotis macrotis, Mindanao, A. Greensmith (BLSA 34287). G, Lyncornis macrotis macropterus, Tangkoko Batuangus, Sulawesi, G. Sangster (GS 1841).
Figure 8 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 8. Integrative taxonomy of Lyncornis nightjars, illustrating contrasting sensitivities of datasets and the failure of each dataset to recover all five species.
Figure 3 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 3. Maximum likelihood tree of cytochrome b sequences of the genus Lyncornis and various outgroups. Bootstrap proportions (> 70%) and posterior probabilities (> 0.8) are indicated above and below branches, respectively.
Figure 1 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 1. Map showing range of currently recognized taxa in the Lyncornis macrotis complex. Taxonomy follows Cleere (1998).
Figure 7 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 7. Upper tail of four taxa in the Lyncornis macrotis complex, illustrating differences in pattern and coloration. Note the marked differences in pattern and coloration between L. m. cerviniceps and L. m. jacobsoni. G. Sangster/©Naturalis Biodiversity Center, Leiden.
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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
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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.