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Fig. 21 in Phylogenetic Studies On Didelphid Marsupials Ii. Nonmolecular Data And New Irbp Sequences: Separate And Combined Analyses Of Didelphine Relationships With Denser Taxon Sampling
Fig. 21. Strict consensus of 34 equally mostparsimonious trees obtained by a heuristic analysis of the combined data (nonmolecular characters plus IRBP2) described in this report. Bremer support and bootstrap values are provided above and below each branch, respectively. Outgroup taxa are indicated with asterisks. Parsimonyequivalent resolutions of the basal ingroup polytomy are illustrated in figure 19D, E, and F. Parsimonyequivalent resolutions of the ''other Marmosa'' + Micoureus polytomy are shown in figure 22.
FIG. 11 in Phylogenetic Relationships of New World Porcupines (Rodentia, Erethizontidae): Implications for Taxonomy, Morphological Evolution, and Biogeography
FIG. 11. Camera-trap photograph of two Coendou bicolor visiting a mineral lick near the Centro de Investigación Río Los Amigos, Madre de Dios, Peru (courtesy of Dyana LaRosa). In situations like this, porcupines are probably exposed to a greater risk of predation than they would be in the canopy. Coendou prehensilis is the only other Neotropical species known to frequent mineral licks (Montenegro, 2004; Blake et al., 2011).
Fig. 11. Anthrenocerus stigmacrophilus. Lateral habitus. Scale line 0.5 in Description of the Larval Stage ofMyrmeanthrenus frontalisArmstrong andAnthrenocerus stigmacrophilusArmstrong (Coleoptera: Dermestidae), with a Discussion of their Phylogenetic Relationships
Fig. 11. Anthrenocerus stigmacrophilus. Lateral habitus. Scale line 0.5 mm.
Fig. 1. Myrmeanthrenus frontalis. Lateral habitus. Scale line 1 in Description of the Larval Stage ofMyrmeanthrenus frontalisArmstrong andAnthrenocerus stigmacrophilusArmstrong (Coleoptera: Dermestidae), with a Discussion of their Phylogenetic Relationships
Fig. 1. Myrmeanthrenus frontalis. Lateral habitus. Scale line 1 mm.
FIGURE 15 in Phylogenetic Relationships Of A New Genus Of Calliopsine Bees From Peru, With A Review Of Spinoliella Ashmead (Hymenoptera: Andrenidae)
FIGURE 15. Male paratype of Spinoliella packeri Gonzalez and Engel, new species. A. Facial view. B. Ventral view of head showing hypostomal carina projecting anteriorly (arrows). C. Dorsal habitus. D. Metabasitibial plate. E. Lateral habitus. F. Metasoma in dorsal view. G. Metasomal S7. H. Metasomal S8. I. Genital capsule in dorsal (left half) and ventral (right half) views. J. Lateral aspect of genital capsule.
FIGURE 10 in Phylogenetic Relationships Of A New Genus Of Calliopsine Bees From Peru, With A Review Of Spinoliella Ashmead (Hymenoptera: Andrenidae)
FIGURE 10. Male of Spinoliella longirostris Toro from Q. Paposo, Region II, Chile (AMNH). A. Facial view. B. Lateral view of head.
FIGURE 4 in Phylogenetic Relationships Of A New Genus Of Calliopsine Bees From Peru, With A Review Of Spinoliella Ashmead (Hymenoptera: Andrenidae)
FIGURE 4. Female holotype of Spinoliella aidae Gonzalez, Smith-Pardo, and Engel, new species. A. Facial view. B. Detail of face. C. Metabasitibial plate. D. Dorsal habitus. E. Detail of mesoscutum, mesoscutellum, metanotum, and propodeum in dorsal view. F. Lateral habitus. G. Terminal metasomal terga.
Figure 3 in Phylogenetic relationships and systematics of the jumping spider genus Colopsus with the description of eight new species from Sri Lanka (Araneae: Salticidae)
Figure 3. Photographs of live Colopsus cancellatus from Ethagala; (a–d). Male, (e–h). Female.
Figure 6 in Phylogenetic relationships of thorny catfishes (Siluriformes: Doradidae) inferred from molecular and morphological data
Figure 6. Maximum likelihood tree of Doradidae inferred from nuclear EF1a intron and exon sequence data. Numbers at nodes represent Bayesian posterior probability percentages, ML bootstrap (500 pseudoreplicates) values, MP bootstrap (1000 pseudoreplicates) values. Nodes without support values represent <50% support obtained by each method (Bayesian, ML, MP). This is an unrooted tree; the black star indicates the hypothetical attachment point of the root (see Fig. 7).
Figure 35 in Phylogenetic relationships of the suckermouth armoured catfishes (Loricariidae) with emphasis on the Hypostominae and the Ancistrinae
Figure 35. Inner dentary teeth, right side, ventral view. A, Hypostomus plecostomus 3, INHS 28903. B, Hypostomus hemicochliodon, FMNH 97010. C, Hypostomus plecostomoides (H. cochliodon group), INHS 59831. D, Scobinancistrus pariolispos Isbrücker and Nijssen, ZMA uncatalogued. Scale bars = 0.5 mm.
Figure 7 in Phylogenetic relationships of the suckermouth armoured catfishes (Loricariidae) with emphasis on the Hypostominae and the Ancistrinae
Figure 7. Phylogeny of the Rhinelepis group from Armbruster (1998b) based on osteology and digestive tract anatomy.
Figure 23 in Phylogenetic relationships of the suckermouth armoured catfishes (Loricariidae) with emphasis on the Hypostominae and the Ancistrinae
Figure 23. Sphenotic, right side, dorsolateral view. A, Ancistrus pirareta, UMMZ 206085. B, Chaetostoma anomala, INHS 69496. C, Panaque albomaculatus, FMNH 96951. Scale bars = 1 mm. Drawings sized such that the lengths of the orbits are the same.
Figure 8 in Cranial osteology and phylogenetic relationships of Hamadasuchus rebouli (Crocodyliformes: Mesoeucrocodylia) from the Cretaceous of Morocco
Figure 8. Results of phylogenetic analysis. A, strict consensus of the 48 most parsimonious trees with all taxa included. Tree length is 548 steps, consistency index is 0.3923, retention index is 0.6623, and rescaled consistency index is 0.2598. Bootstrap support values are given above each branch for values greater than 50%. Bremer decay values are given below each branch. B, Adams consensus of the same set of trees with Adams decay values below each branch. C, strict consensus of the 138 most parsimonious trees of the reduced taxon set. Tree length is 540 steps, consistency index is 0.3981, retention index is 0.6546, and rescaled consistency index is 0.2606. Bootstrap support values greater than 50% are presented above each branch and Bremer decay values below each branch. D, Adams consensus of this set of trees with Adams decay values below each branch.
Figure 1. Phylogenetic diagram showing hypothesized relationships between the 14 in Bivalvia - a look at the Branches
Figure 1. Phylogenetic diagram showing hypothesized relationships between the 14 nominal major clades here recognized for the living members of the molluscan class Bivalvia. Shaded boxes indicate branches that are treated in whole or part in this volume.
Fig. 22 in Descriptive morphology and phylogenetic relationships among species of the Neotropical annual killifish genera Nematolebias and Simpsonichthys (Cyprinodontiformes: Aplocheiloidei: Rivulidae)
Fig. 22. Strict consensus of six equally parsimonious shortest phylogenies (L = 297; CI = 0.53; RI = 0.79). Letters left of branches represent different clades of the strict consensus tree, and numbers left of branches are bootstrap values. List of apomorphies by node is presented in Appendix III.
Fig. 4 in Descriptive morphology and phylogenetic relationships among species of the Neotropical annual killifish genera Nematolebias and Simpsonichthys (Cyprinodontiformes: Aplocheiloidei: Rivulidae)
Fig. 4. Urogenital region, pelvic and anal fins in Nematolebias and Simpsonichthys. (a) pelvic-fin insertion, ventral view, of N. papilliferus, male, UFRJ 5361; (b) pelvic fin and urogenital papilla, lateral view, of N. papilliferus, male, UFRJ 5361; (c) pelvic fin and urogenital papilla, lateral view, of N. papilliferus, female, UFRJ 5361; (d) pelvic fin and urogenital papilla, lateral view, of S. semiocellatus, male, UFRJ 3933; (e) posterior margin of the anal-fin, lateral view, of S. myersi, female, UFRJ 4760. AF = anal fin; PF = pelvic fin; UP = urogenital papilla. Scale bar 1 mm.
Fig. 1 in Descriptive morphology and phylogenetic relationships among species of the Neotropical annual killifish genera Nematolebias and Simpsonichthys (Cyprinodontiformes: Aplocheiloidei: Rivulidae)
Fig. 1. Diagrammatic representation of cephalic structures of Nematolebias papilliferus, including latero-sensory system and cephalic squamation; UFRJ 5295, male, 36.1 mm SL. (a) lateral view; (b) dorsal view; (c) ventral view. ais = anterior infraorbital series; an = anterior naris; arn = anterior rostral neuromast; lal = lateral line neuromasts; lms = lateral mandibular series; mas = mandibular series; mis = median infraorbital series; mon = median opercular series; nai = neuromast anterior to infraorbital series; ots = otic series; pan = parietal neuromast; pbs = preorbital series; pis = posterior infraorbital series; pmn = paramandibular neuromast; pn = posterior naris; pos = post-otic series; prn = posterior rostral neuromast; prs = preopercular series; sos = supraorbital series; stn = supra-temporal neuromast; vos = ventral opercular series; A- H = frontal scales A-H; in bold, frontal scale with all borders free.
FIG. 32. Digital 3D in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate
FIG. 32. Digital 3D reconstructions of the osseous labyrinths of Cochilius volvens AMNH VP-29651, Tetramerorhinus lucarius AMNH VP-9245, Tapirus indicus AMNH M-200300, Ceratotherium simum AMNH M-51882, and Equus caballus AMNH M-204155 (above and on opposite page), in lateral, ventral, and dorsal views. In each ventral view, arrow indicates position of fenestra cochleae.
FIG. 28 in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate
FIG. 28. Homalodotherium sp. MPM PV 17490, oblique caudoventral aspect. Patterson (1934a) claimed that in this taxon a carotid foramen existed on bulla's caudal surface, lying close to jugular area of basicapsular fenestra. In this specimen, only transbullar aperture in this location (asterisk) is very small and more readily interpreted as a canaliculus for tympanic nerve. If adult Homalodotherium possessed an intact internal carotid artery at all (see p. 114), it must have entered endocranium through exposed rostral part of basicapsular fenestra (not visible from this angle), as in Toxodon (see fig. 29). Note fully caudal position of posttemporal foramen, as in other notoungulates (cf. fig. 30).
FIG. 33 in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate
FIG. 33. Stapes in selected members of comparative set. Top: Digital 3-D reconstruction of left stapes of Astrapotherium magnum MACN A 3208 in A, medial; B, tympanic; C, lateral; D, vestibular views. E, Dislocated stapes lodged in vestibule of left osseous labyrinth of MACN A 3208 (note scale). Bottom: Left stapes of Tapirus indicus (F) and Equus caballus (G) in medial and distal views (after Fleischer, 1973: figs. 48, 49). All to same scale as Astrapotherium.
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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.
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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.
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