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608 results for “Species recognition”
FIGURE 22. Komarkovaea angustata. A–B in Revision of the Synechococcales (Cyanobacteria) through recognition of four families including Oculatellaceae fam. nov. and Trichocoleaceae fam. nov. and six new genera containing 14 species
FIGURE 22. Komarkovaea angustata. A–B. Variation in trichome width between mature and young filament or hormogonia. C. Variation in cell shapes between young and mature trichomes: isodiametric, slightly longer than width or barrel-shaped, and abundance of necridia in mature trichomes. D. Rapid regional cell division along trichomes resulting in basal and apical parts of filaments. E. Reddish small granules occassionaly observed on cells. Scale bar 10μm in 1000X magnification.
FIGURE 21. Tildeniella nuda. A in Revision of the Synechococcales (Cyanobacteria) through recognition of four families including Oculatellaceae fam. nov. and Trichocoleaceae fam. nov. and six new genera containing 14 species
FIGURE 21. Tildeniella nuda. A. Filaments short, Pseudanabaena-like, trichomes not or only slight constricted, connected by somewhat translucent cell wall; B–H. Cells sometimes distinctively elongated, bent or involuted (arrows). Scale bar 10μm in 1000X magnification.
FIGURE 11. Pegethrix olivacea. A–D in Revision of the Synechococcales (Cyanobacteria) through recognition of four families including Oculatellaceae fam. nov. and Trichocoleaceae fam. nov. and six new genera containing 14 species
FIGURE 11. Pegethrix olivacea. A–D. Irregular filament shapes due to uneven cell division events along trichome. E. Single falsebranching filament. F. Nodule formation. G–K. Irregular cell shape and trichome length, hormogonia few-celled, abundant. Scale bar 10μm in 1000X magnification.
FIGURE 20. Tildeniella torsiva. A in Revision of the Synechococcales (Cyanobacteria) through recognition of four families including Oculatellaceae fam. nov. and Trichocoleaceae fam. nov. and six new genera containing 14 species
FIGURE 20. Tildeniella torsiva. A. Single false-branching very rarely observed, only in senescing culture. B. Cells isodiametric to slightly longer than width. C–D. Filaments sometimes wavy to strongly spirally coiled. Scale bar 10μm in 1000X magnification.
Fig. 5 in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
Fig. 5. PCA of environmental envelopes for four Hibiscus krichauffianus sens. lat. specimens sorted by morphotype groupings. Morphotype A, grey squares; Morphotype B, orange circles; Morphotype C, blue triangles; and Morphotype D, black crosses.
Fig. 4 in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
Fig. 4. Habit of morphotypes A–C. (a) Morphotype A Hibiscus krichauffianus sens. strict. (voucher: D.E.Albrecht 16356, CANB; images: Dave Albrecht); (b) morphotype B Hibiscus verecundus (voucher: T.G.B.McLay TM333, CANB; images: Mike Bayly); and (c) morphotype C Hibiscus calcareus (voucher: D.E.Albrecht 16345, CANB [holotype]; images: Dave Albrecht).
Fig. 1 in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
Fig. 1. Distribution map for the four morphotypes of H. krichauffianus sens. lat. in Australia. Distributions are based only on material viewed by the authors. Morphotype A: Hibiscus krichauffianus sens. strict., grey squares; Morphotype B: Hibiscus verecundus, orange circles; Morphotype C: Hibiscus calcareus, blue triangles; Morphotype D: Hibiscus sp. Belele (voucher: D.W.Goodall 3417), black crosses.
Fig. 2 in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
Fig. 2. Example herbarium specimens of the four morphotypes of H. krichauffianus sens. lat. (a) Morphotype A Hibiscus krichauffianus sens. strict. (voucher: C.J.Brodie & P.J.Lang 3402, AD 249644); (b) morphotype B Hibiscus verecundus (voucher: R.J.Fensham 2991, BRI AQ653057); (c) morphotype C Hibiscus calcareus (voucher: P.Hudson s.n., AD 98321044); and (d) morphotype D Hibiscus sp. Belele (voucher: D.W.Goodall 3417, PERTH 3427285). Scale bar: 2 cm.
Fig. 3 in Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus
Fig. 3. Seeds of the four morphotypes. (a) Morphotype A Hibiscus krichauffianus sens. strict. (voucher: C.J.Brodie & P.J.Lang 3402, AD 249644); (b) morphotype B Hibiscus verecundus (voucher: R.J.Fensham 2991, BRI AQ653057); (c) morphotype C Hibiscus calcareus (voucher: P.Hudson s.n., AD 98321044); and (d) morphotype D Hibiscus sp. Belele (voucher: D.W.Goodall 3417, PERTH 3427285). Scale bar: 1 mm.
FIGURE 3. Bessera elegantissima. A in Morphological variation in Bessera (Asparagaceae: Brodiaeoideae) allows for the recognition of two new species
FIGURE 3. Bessera elegantissima. A. Complete plant with corms, leaves, inflorescence and flowers. B. Dissected flower. C. Flower, lateral view. D. Membranous staminal tube with filaments and anthers. E. Fruit. F. Seeds. Watercolor illustration by Fátima Bracamontes.
FIGURE 1 in Morphological variation in Bessera (Asparagaceae: Brodiaeoideae) allows for the recognition of two new species
FIGURE 1. Geographic distribution of the genus Bessera. Red circles = B. elegans, fuchsia squares = B. elegantissima, blue rhombuses = B. ramirezii, and lilac triangles = B. tuitensis.
FIGURE 5. Bessera ramirezii. A in Morphological variation in Bessera (Asparagaceae: Brodiaeoideae) allows for the recognition of two new species
FIGURE 5. Bessera ramirezii. A. Complete plant with corms, leaves, inflorescence, flowers, and detail of scabrous scape at the base. B. Dissected flower. C. Flower, lateral view. D. Membranous staminal tube with filaments and anthers. E. Fruit. F. Seed. Watercolor illustration by Fátima Bracamontes.
FIGURE 4. A in Morphological variation in Bessera (Asparagaceae: Brodiaeoideae) allows for the recognition of two new species
FIGURE 4. A. Bessera elegantissima, different perianth colors found in a single locality. B. elegantissima showing two different perianth and anther colors. C. Close-up of Bessera ramirezii, showing membranous staminal tube, flat filaments and anthers. D. B. ramirezii inflorescence showing some open flowers. E. Typical scarlet perianth of Bessera elegans. F. Bessera tuitensis inflorescence and flowers. Photos by Juan Pablo Ortiz-Brunel (C–F) and Eduardo Ruiz-Sanchez (A, B).
FIGURE 2 in Morphological variation in Bessera (Asparagaceae: Brodiaeoideae) allows for the recognition of two new species
FIGURE 2. Box-plots for five characters that were significantly different among species (P <0.05). A. Filament length. B. Leaf length. C. Tube length. D. Leaf width. E. Pedicel length. Boxes represent 75% of the variation and horizontal bars the other 25%; middle lines indicate the mean; whiskers indicate the range of the data; and dots indicate outliers. F. Discriminant analysis. Red circles = Bessera elegans, fuchsia squares = B. elegantissima, blue rhombuses = B. ramirezii, lilac triangles = B. tuitensis. Black crosses are the centroids for each species.
FIGURE 9 in Evidence for the recognition of two species of Anolis formerly referred to as A. tropidogaster (Squamata: Dactyloidae)
FIGURE 9. Designation of nasal scalation types. (a) Nasal type 1 (MHCH 1636); (b) Nasal type 2 (SMF 91901). Scale bars = 1.0 mm. See Text for details.
FIGURE 5 in Evidence for the recognition of two species of Anolis formerly referred to as A. tropidogaster (Squamata: Dactyloidae)
FIGURE 5. Results of 16S mtDNA analysis. a) Consensus tree from Maximum Likelihood analysis. Scale bar refers to substitutions per site. Bootstrap support values above nodes correspond to Maximum Likelihood analysis, those below the nodes to the Maximum Parsimony consensus tree of exactly the same topology. (b) Parsimony network derived from the same alignment, each node representing a unique haplotype.
FIGURE 2 in Evidence for the recognition of two species of Anolis formerly referred to as A. tropidogaster (Squamata: Dactyloidae)
FIGURE 2. Map indicating known collecting sites mentioned in text of anoles formerly referred to as Anolis tropidogaster. Each symbol can represent one or more nearby localities. Circles: Type A hemipenes; squares: Type B hemipenes; triangles: localities of Anolis tropidogaster-like specimens not verified by authors (sources: MHUA catalogue, Donoso-Barros 1968, Carvajal-Cogollo and Urbina-Cardona 2008). See text for details.
FIGURE 1 in Evidence for the recognition of two species of Anolis formerly referred to as A. tropidogaster (Squamata: Dactyloidae)
FIGURE 1. (a) Type A hemipenis (SMF 91956); (b) Type B hemipenis (SMF 91902). See text for details. Scale bar = 1.0 mm.
FIGURE 13 in Evidence for the recognition of two species of Anolis formerly referred to as A. tropidogaster (Squamata: Dactyloidae)
FIGURE 13. Map indicating collecting sites of selected lowland anoles inhabiting the Pacific versant of Panama and Costa Rica. Each symbol can represent one or more nearby localities. Circles: Anolis tropidogaster; squares: A. gaigei; white triangles: localities of A. tropidogaster-like specimens not verified by authors; black inverted triangles: A. polylepis; stars: A. osa; hexagons: A. cupreus. See text for details.
FIGURE 4 in Evidence for the recognition of two species of Anolis formerly referred to as A. tropidogaster (Squamata: Dactyloidae)
FIGURE 4. Comparison of scalation details in Anolis gaigei (left column) and A. tropidogaster (right column). Dorsal head in (a) A. gaigei SMF 91956 and (b) A. tropidogaster MHCH 1701. Cloacal region in (c) A. gaigei SMF 82705 and (d) A. tropidogaster FMNH 63793. Dorsal tail in (e) A. gaigei SMF 91956 and (f) A. tropidogaster MHCH 1636. Chin region in (g) A. gaigei SMF 91956 and (h) A. tropidogaster MHCH 1640.
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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.