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71 results for “Stromateiformes”
Figure 70 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 70. Unambiguous phenotypic synapomorphies for Stromateiformes superimposed on the reference tree of the order obtained under implied-weights parsimony (k = 13.56554).
Figure 67 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 67. Reference tree obtained under implied-weights parsimony (k = 13.56554), with sensitivity analysis of alternative weighting schemes, highlighting the interrelationships of node 82. Squares representing each value of k are coloured according to their respective element-based scores. Numbers below sensitivity plots indicate the average element-based comparison score for the clade. Node numbers referenced in the text displayed above each clade.
Figure 66 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 66. Reference tree (A) with the highest global topological similarity and nodal stability (implied-weights parsimony, with k = 13.56554), obtained by pairwise comparisons of the 11 tested trees organized in descending order of their average element-based comparison scores (B) and in ascending order of the standard deviation of the element-based comparison scores (C). The root taxon (Beryx splendens) is not represented in this tree.
Figure 65 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 65. Examples of the association between juvenile fishes and pelagic, gelatinous invertebrates. A, B, the nomeid Nomeus gronovii sheltering inside a pyrosome (A) and swimming around the tentacles of a pelagic siphonophore (B). C, the amarsipid Amarsipus carlsbergi hiding in the abdominal cavity of a pelagic salp. D, a bramid Brama sp. resting on the top of a jellyfish. Images from Suzan Meldonian (A) and Linda Ianniello (B–D).
Figure 71 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 71. Left lateral view of preserved specimen of the tetragonurid Tetragonurus cuvieri (MZUSP 123241, 94.7 mm standard length; A) and the amarsipid Amarsipus carlsbergi (SIO 75-122, 50.4 mm standard length; B).
Figure 62 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 62. Diagrammatic cross-sections of the pharyngeal sac of the ariommatid Ariomma indicum (A), the stromateid Stromateus fiatola (B), the centrolophid Centrolophus niger (C) and the nomeid Cubiceps capensis (D). The pointy projections emerging from the internal walls of the pharyngeal sac (A–D) represent the sac papillae, and arrows (in C, D) indicate the greatly enlarged, posteriorly directed, toothed gill rakers. In ariommatids (A) and stromateids (B), the internal lining of the sac is classified as papillary (or polypoid), whereas the presence of enlarged rakers entering the pharyngeal sac of centrolophids (C) and nomeids (D) gives the sac a folded (or wrinkled) aspect. The obliquely shaded oval structures (C, D) represent the elongated fourth upper pharyngeal tooth plates. They are not shown in ariommatids (A) and stromateids (B) because they extend only into the anterior half of the sac. Figure modified from Barnard (1948: fig. 10).
Figure 63 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 63. Intradermal canal plexus of the centrolophid Tubbia tasmanica (CSIRO H 6979-03, 325.2 mm standard length). A, intradermal canals in a radiographed specimen. B, transverse section of the superficial layers of skin and axial musculature. C, high magnification of external appearance of skin surface. D, internal surface of the same piece. Visible pores connect the external surface to the interdermal space (C, D). Scale bars: 1 mm (in B–D).
Figure 59 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 59. Rakers from ceratobranchials and pharyngeal sac of the centrolophid Psenopsis anomala (MZUSP 119730; A–D) and the ariommatid Ariomma bondi (MZUSP 86717; E–H). A, E, rakers from with outer face of ceratobranchial 1. B, F, rakers from inner face of ceratobranchial 1. C, G, rakers from outer face of ceratobranchial 5. D, H, pharyngeal-sac rakers. Scale bars: 0.5 mm.
Figure 60 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 60. Stromateiform pharyngeal-sac rakers in dorsal (A, C, E) and lateral (B, D, F) view. A, B, the ariommatid Ariomma bondi (MZUSP 86717), showing round base and elongate axis. C, D, the stromateid Peprilus triacanthus (MZUSP 123240), showing stellate base and elongate axis. E, F, the nomeid Psenes cyanophrys (MZUSP 106392), showing stellate base and less elongate axis. Scale bars: 0.5 mm.
Figure 58 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 58. Micro-computed tomography scans of pharyngeal-sac skeletons in left lateral view, whole (A, C) and sagittal (B, D) view. A, B, the ariommatid Ariomma bondi (MZUSP 86717). C, D, the stromateid Peprilus triacanthus (MZUSP 123240). Scale bar: 2 mm.
Figure 64 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 64. Photographs of Alizarin Red-stained percomorph scales. Posterior margin of a cycloid scale of the nomeid Cubiceps whiteleggii (MZUSP 67590; A), a spinoid scale of the berycid Beryx splendens (MZUSP 121649; B) and a transforming ctenoid scale of the apogonid Apogon maculatus (MZUSP 43155; C). Scale sampling was standardized to underneath the left pectoral-fin rays. Scale bars: 0.5 mm.
Figure 69 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 69. Reference tree obtained under implied-weights parsimony (k = 13.56554), with sensitivity analysis of alternative weighting schemes, highlighting the interrelationships of Stromateiformes (node 90). Squares representing each value of k are coloured according to their respective element-based scores. Numbers below sensitivity plots indicate the average element-based comparison score for the clade. Node numbers referenced in the text displayed above each clade.
Figure 57 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 57. Branchial and pharyngeal-sac musculoskeletal system of the stromateid Stromateus brasiliensis (MZUSP 51279) in dorsal (A), lateral (B) and ventral (C) view. Arrow indicates posterolateral set of sphincter oesophagi fibres. Scale bar: 5 mm.
Figure 56 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 56. Branchial and pharyngeal-sac musculoskeletal system of the nomeid Cubiceps whiteleggii (MZUSP 67590) in dorsal (A), lateral (B) and ventral (C) view. Scale bar: 6 mm.
Figure 55 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 55. Branchial and pharyngeal-sac musculoskeletal system of the centrolophid Icichthys lockingtoni (OS 16732) in dorsal (A), lateral (B) and ventral (C) view. Scale bar: 5 mm.
Figure 54 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 54. Dorsal view of branchial and pharyngeal-sac musculoskeletal system of the ariommatid Ariomma melana (MZUSP 123246; A) and the centrolophid Hyperoglyphe perciformis (MZUSP 119733; B). Scale bars: 5 mm. Arrow points to the dorsal expansion of the pharyngeal sac.
Figure 53. A in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 53. A, cranial and abdominal anatomy of the tetragonurid Tetragonurus cuvieri (MZUSP 123241). Gill arches, pharyngeal sac and anterior portion of the abdominal cavity (orbital, adductor mandibulae, opercular, hyopalatal and pectoral girdle complexes removed). Scale bar: 10 mm (in A). B, higher magnification of the gill arch muscles and bones. Scale bar: 2 mm (in B). C, higher magnification pharyngeal sac and anteriormost abdominal organs. Scale bar: 2 mm (in C).
Figure 49 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 49. Left adductor mandibulae and associated structures of the trichiurid Trichiurus lepturus (MZUSP 8855) in medial (A) and lateral (B) view. Scale bar: 10 mm.
Figure 45 in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 45. The dorsal fin of a cleared and stained Peprilus sp. (SML 34163), depicting the blade-like anteriormost dorsal-fin spines. Arrows indicate to two anteriormost dorsal-fin spines. Photograph taken by Miguel Montalvo. Scale bar: 0.5 mm.
Figure 40. A, B in Comprehensive phenotypic phylogenetic analysis supports the monophyly of stromateiform fishes (Teleostei: Percomorphacea)
Figure 40. A, B, micro-computed tomography scan of the branchial and pharyngeal-sac skeleton of the nomeid Psenes cyanophrys (MZUSP 106392) in dorsal (A) and left lateral (B) view. Scale bar: 4 mm (in B). C, magnification of third pharyngobranchial and associated pharyngeal tooth plate in ventral view. Scale bar: 1 mm (in C).
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