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450 results for “external morphology”
Fig. 8 in External morphology, postcranial and appendicular osteology of three southwestern Atlantic flatfishes (Paralichthys, Paralichthyidae), and comparisons with other congeneric species
Fig. 8. Relationships of interorbital width to head length in Paralichthys californicus, P. dentatus, P. lethostigma, P. oblongus, P. orbignyanus, P. squamilentus, P. triocellatus, P. tropicus and P. woolmani.
Fig. 3 in External morphology, postcranial and appendicular osteology of three southwestern Atlantic flatfishes (Paralichthys, Paralichthyidae), and comparisons with other congeneric species
Fig. 3. Skeleton of the precaudal vertebrae region of Paralichthys isosceles (a); P. orbignyanus (b and d); and P. patagonicus (c). See abbreviations in text. Scale bar indicates 1 mm.
Fig. 1 in External morphology, postcranial and appendicular osteology of three southwestern Atlantic flatfishes (Paralichthys, Paralichthyidae), and comparisons with other congeneric species
Fig. 1. Photographs of three flatfishes of Paralichthys from the Southwestern Atlantic: a. Paralichthys isosceles, b. Paralichthys orbignyanus, c. Paralichthys patagonicus. Scale bar indicates 5 cm.
Figure 1 in Phylogenetic analysis of the myrmecophilous Cremastocheilus Knoch (Coleoptera, Scarabaeidae, Cetoniinae), based on external adult morphology
Figure 1. Strict consensus of 24 equally parsimonious trees (153 steps, CI = 0.46, RI = 0.80) of Cremastocheilus. Dark bars indicate monophyletic groups that correspond with Alpert's (1994) subgenera and respective species groups. Jackknife values are shown above branches, with support <50 not shown. Bremer support values are shown in bold below branches. Black dot indicates the genus Cremastocheilus.
Text-fig. 1. Diplopanax cacaoides (ZENKER) comb. nov. a–d: [Holotype of Mastixia cantia E.REID et M.CHANDLER, V.22953]. a: Lateral view of longitudinally broken specimen, reflected light. b–d: Surface renderings from micro-CT data. b: Lateral view of longitudinal fracture surface. c: Same specimen rotated to show external surface. d: Enlargement of lower half from (a, b), reflected light. e, f: Specimen figured originally as a paratype of M. cantia, V.22954 (Reid and Chandler 1933: pl. 25, fig. 3), reflected light. e: Ventral view with much of the endocarp wall fallen away exposing smooth convex ventral surface of locule cast. f: Transversely fractured surface, showing thick wall of the endocarp, and dehiscence plane leading to the left limb of the locule. g: Transversely sectioned, laterally compressed specimen from Miocene of Wiesa, Germany for comparison, Senckenberg Museum, SM.B. 21034/I. h–j: Digital transverse sections from micro-CT data of the Holotype V.22953. h: Transverse fracture surface from (b), showing curved locule and zone of weakness defining the germination valve (arrow), reflected light. i: Same orientation with clear demarcation of the separation plane of the germination valve (arrow), digital section from micro-CT scan. j: Enlargement from (h). Scale bars 5 mm. in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision
Text-fig. 1. Diplopanax cacaoides (ZENKER) comb. nov. a–d: [Holotype of Mastixia cantia E.REID et M.CHANDLER, V.22953]. a: Lateral view of longitudinally broken specimen, reflected light. b–d: Surface renderings from micro-CT data. b: Lateral view of longitudinal fracture surface. c: Same specimen rotated to show external surface. d: Enlargement of lower half from (a, b), reflected light. e, f: Specimen figured originally as a paratype of M. cantia, V.22954 (Reid and Chandler 1933: pl. 25, fig. 3), reflected light. e: Ventral view with much of the endocarp wall fallen away exposing smooth convex ventral surface of locule cast. f: Transversely fractured surface, showing thick wall of the endocarp, and dehiscence plane leading to the left limb of the locule. g: Transversely sectioned, laterally compressed specimen from Miocene of Wiesa, Germany for comparison, Senckenberg Museum, SM.B. 21034/I. h–j: Digital transverse sections from micro-CT data of the Holotype V.22953. h: Transverse fracture surface from (b), showing curved locule and zone of weakness defining the germination valve (arrow), reflected light. i: Same orientation with clear demarcation of the separation plane of the germination valve (arrow), digital section from micro-CT scan. j: Enlargement from (h). Scale bars 5 mm.
Рис. 4. Микроскульптура наружной поверхности глохидиальных створок перловиц Nodularia biwae (A, D – увеличенный фрагмент) и Lanceolaria grayana (B, C – увеличенный фрагмент) иЗ Японии, о-в Хонсю. СканируюЩаЯ ЭлектроннаЯ микроскопиЯ. МасШтаб 1 мкм (А, В) и 2 мкм (C, D). Fig. 4. Microsculpture of external surface of glochidia of mussels Nodularia biwae (A, D – fragment) and Lanceolaria grayana (B, C – fragment) from Honshu Is., Japan. Scanning electron microscopy. Scale bar 1µm (А, В) and 2 µm (C, D). in Morphology of glochidia of the freshwater mussels Nodularia amurensis and Middendorffinaia sujfunensis (Bivalvia: Unionidae: Nodulariinae) from the Russian Far East
Рис. 4. Микроскульптура наружной поверхности глохидиальных створок перловиц Nodularia biwae (A, D – увеличенный фрагмент) и Lanceolaria grayana (B, C – увеличенный фрагмент) иЗ Японии, о-в Хонсю. СканируюЩаЯ ЭлектроннаЯ микроскопиЯ. МасШтаб 1 мкм (А, В) и 2 мкм (C, D). Fig. 4. Microsculpture of external surface of glochidia of mussels Nodularia biwae (A, D – fragment) and Lanceolaria grayana (B, C – fragment) from Honshu Is., Japan. Scanning electron microscopy. Scale bar 1µm (А, В) and 2 µm (C, D).
FIGURE 23. Palissya batrumi 1. Specimen showing external morphology, LX721 in Middle-Late Jurassic plant assemblages of the Catlins coast, New Zealand
FIGURE 23. Palissya batrumi 1. Specimen showing external morphology, LX721, Little Beach (Note adjacent Pityophyllum); 2. Specimen with apical part split longitudinally, revealing the axis, LX1096, Curio Bay.; 3. Specimen weathered to reveal the adaxial surface with paired ovule/scale units, LX2238, Otara-20. All scale bars equal 10 mm.
Figs. 61–62 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 61–62. Male genitalia of species of Siderone Hübner, [1823] in lateral view. 61: Siderone galanthis catarina Dottax and Pierre, 2009 comb. nov. (Santa Catarina, Brazil). 62: Siderone syntyche mars Bates, 1860 (Huánuco, Peru). Scale bar = 1 mm.
Fig. 58. Neighbor joining tree using Kimura-2 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Fig. 58. Neighbor joining tree using Kimura-2-Parameter distance model of 37 sequences of species of Siderone Hübner [1823] and Coenophlebia C. Felder and R. Felder, 1862, with 658 base pairs of the mitochondrial gene cytochrome oxidase, Subunit I. Scale bar = 1% of distance.
Figs. 33–36 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 33–36. Head capsules of fifth instars in anterior and lateral views. 33 and 34: Zaretis strigosus (Gmelin, [1790]). 35 and 36: Siderone galanthis catarina Dottax and Pierre, 2009 comb. nov. Scale bar = 1 mm.
Figs. 44–57 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 44–57. Host plant and immature stages of Siderone galanthis catarina Dottax and Pierre, 2009 comb. nov. 44: Host plant, Casearia sylvestris (Salicaceae). 45: Egg, lateral. 46: Second instar resting in frass chain. 47: Second instar, dorsal. 48 and 49: Third instar, lateral and dorsal. 50 and 51: Fourth instar, lateral and dorsal. 52 and 53: Fifth instar, lateral and dorsal. 54: Fifth instar, head capsule in anterior view. 55 and 56: Pupa, ventral, dorsal and lateral views. Scale bars = 1 mm.
Figs. 5–8 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 5–8. Siderone galanthis catarina Dottax and Pierre, 2009 comb. nov. (Santa Catarina, Brazil). 5 and 6: Male, dorsal and ventral. 7 and 8: Female, dorsal and ventral. Scale bar = 1 cm.
Figs. 9–22 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 9–22. Immature stages of Zaretis strigosus (Gmelin, [1790). 9 and 10: First instar, lateral and dorsal. 11 and 12: Second instar, lateral and dorsal. 13 and 14: Third instar, lateral and dorsal. 15 and 16: Fourth instar, lateral and dorsal. 17 and 18: Fifth instar, lateral and dorsal. 19: Fifth instar, head capsule, anterior view. 20–22: Pupa, ventral, dorsal and lateral views. Scale bars = 1 mm.
Figs. 23–26 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 23–26. Schematics of the first instar of Zaretis strigosus (Gmelin, [1790]) and Siderone galanthis catarina Dottax and Pierre, 2009 comb. nov. 23 and 24: Head capsule, anterior and posterior. 25: Prothoracic plate, dorsal. 26: Thorax and abdomen, lateral.
Figs. 1–4 in External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae)
Figs. 1–4. Zaretis strigosus (Gmelin, [1790]) (Santa Catarina, Brazil). 1 and 2: Male, dorsal and ventral. 3 and 4: Female, dorsal and ventral. Scale bar = 1 cm.
Figure 2 in The first description of the female external morphology of Bisetocreagris cheni Jia, Zhao & Zhang, 2010 (Pseudoscorpiones, Neobisiidae) from China
Figure 2. Bisetocreagris cheni Jia, Zhao & Zhang, 2010, female: a. carapace, dorsal view; b. right chelicera, dorsal view; c. galea; d. rallum; e. left pedipalpal chela, retro-lateral view; f. left pedipalp without chela, dorsal view; g. genital area, ventral view; h. right leg I, lateral view; i. right leg IV, lateral view. Scale bars: 0.05 mm (c and d) and 0.5 mm (a, b, e–i).
Figure 1 in The first description of the female external morphology of Bisetocreagris cheni Jia, Zhao & Zhang, 2010 (Pseudoscorpiones, Neobisiidae) from China
Figure 1. Bisetocreagris cheni Jia, Zhao & Zhang, 2010, a. male habitus, dorsal view; b. female habitus, dorsal view. Scale bars: 2.00 mm (a, b).
Linked collectors and determiners for: Endangered beauties: micro-CT cranial osteology, molecular genetics and external morphology reveal three new species of chameleons in the Calumma boettgeri complex (Squamata: Chamaeleonidae).
Natural history specimen data linked to collectors and determiners held within, "Endangered beauties: micro-CT cranial osteology, molecular genetics and external morphology reveal three new species of chameleons in the Calumma boettgeri complex (Squamata: Chamaeleonidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/99b3b009-f006-4146-b335-cbfdc2fcd60b">https://bionomia.net/dataset/99b3b009-f006-4146-b335-cbfdc2fcd60b</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/99b3b009-f006-4146-b335-cbfdc2fcd60b">https://gbif.org/dataset/99b3b009-f006-4146-b335-cbfdc2fcd60b</a>. Formatted as a Frictionless Data package.
Figs. 9–10 in The external morphology of eggs of three Rhopalidae species (Hemiptera: Heteroptera) with a review of the eggs of this family
Figs. 9–10. Eggs of Chorosoma schillingi (Schilling, 1829). 9 – apex of micropylar process, most exposed view; 10 – cuticular cap of hatched larva attached to empty egg, with egg burster, most exposed view. Scale = 100 μm for Fig. 10; 10 μm for Fig. 9. Letterings: b – egg burster; o – opening of micropylar process.
Figs. 17–22 in The external morphology of eggs of three Rhopalidae species (Hemiptera: Heteroptera) with a review of the eggs of this family
Figs. 17–22. Eggs of Rhopalus (Aeschyntelus) maculatus (Fieber, 1837). 17 – whole egg, ventral view; 18 – whole egg, lateral view; 19 – empty egg with separated pseudoperculum, ventral view; 20 – anterior pole of egg with two micropylar processes, lateral view; 21 – detail of micropylar process, most exposed view; 22 – detail of part of dorsal egg surface where is egg attached to surface. Scale = 100 μm for Figs. 17–20; 10 μm for Figs. 21–22. Letterings: m1, m2 – micropylar processes; p – pseudoperculum.
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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)
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.