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17 results for “Zeiformes”
Fig. 1 in Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species
Fig. 1. Lateral view of oreosomatids. A, Allocyttus folletti from the Emperor Seamounts, SNFR 22402, 289.8 mm SL; B, Allocyttus verrucosus from New Zealand, NSMT-P 41168, 187.2 mm SL; caudal peduncle of A. folletti; C, SNFR 10560, 293.4 mm SL, Emperor Seamounts, and that of A. verrucosus; D, NSMT-P 41168, 187.2 mm SL, New Zealand; nasal of oreosomatids; E, A. folletti, SNFR 10561, 347 mm SL, Emperor Seamounts; F, A. verrucosus, NSMT-P 113107, 238.4 mm SL, west coast of Australia. Abbreviations: NA, nasal; PN, posterior nostril.
Fig. 3 in Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species
Fig. 3. Lateral aspect (above) and abdomen (below) of Allocyttus folletti. A, SNFR 10560, 293.4 mm SL, Emperor Seamounts; B, CAS-SU 15377, holotype of Allocyttus folletti, off California, traced from Myers (1960: fig. 1). Arrows indicate the rows of scutes.
Fig. 2 in Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species
Fig. 2. Scales on mid-side of body in, (A) Allocyttus folletti, FAKU 72575, 397 mm SL, Emperor Seamounts, and (B) Allocyttus verrucosus, NSMT-P 113107, 238.4 mm SL, Australia; enlarged scales of dorsal-fin base (S-DFB) in (C) A. folletti, SNFR 22403, 289.3 mm SL, Emperor Seamounts, and (D) A. verrucosus, BSKU 48476, 136.5 mm SL, off South Africa.
Figure 4. Diagrammaticfigureofajuvenileof Zenopsis stabilispinosa, AMS I.31147-002 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 4. Diagrammaticfigureofajuvenileof Zenopsis stabilispinosa, AMS I.31147-002 (80.4 mm SL), paratype.
Figure 3 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 3. Diagrammatic figures of anal-fin pterygiophores and spines of 3 species of Zenopsis: A, Z. stabilispinosa, holotype, FAKU 64803 (307.2 mm SL); B, Z. nebulosa, FAKU 64805 (379 mm SL); C, Z. conchifer, RUSI 14070 (135.5 mm SL). Scales indicate 10 mm.
Figure 2 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 2. Diagrammatic figure (A), and teeth on jaws and vomer (B) of the holotype of Zenopsis stabilispinosa sp. nov., FAKU 64803.
Figure 1 in A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia
Figure 1. Zenopsis stabilispinosa sp. nov. Holotype, FAKU 64803 (307.2 mm SL).
FIG. 8 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 8. Comparison of the branching patterns of molecular and combined-data trees produced with different methods. Each family recognized by Tyler et al. (2003) is a different color. Black lines indicate relationships with strong support; gray lines indicate weaker support. (A) Results from maximum likelihood analysis of molecular data. (B) Results from Bayesian inference analysis of molecular data. (C) Results from maximum likelihood analysis of combined morphological and molecular data, including three genera with morphological data only. (D) Results from Bayesian inference analysis of combined morphological and molecular data, including three genera with morphological data only.
FIG. 7 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 7. Combined (total-evidence) molecular and morphological phylogeny of the Zeiformes based on Bayesian inference (BI) using MrBayes v.3.1.2 (Huelsenbeck and Ronquist, 2001; Ronquist and Huelsenbeck, 2003). See Figure 6 for details of outgroup relationships, and see text for detailed methods and assumptions. The combined maximum likelihood (ML) analysis using Garli v2.0 (Zwickl, 2006) produced almost identical topology and very similar relative branch lengths. Taxa with asterisks (*) are of questionable or revised identification. Taxa with two asterisks (**) are those with morphological data only. Support values at nodes are from both analyses, with BI posterior probabilities above ML bootstrap percentages. Numbers after scientific names correspond to code numbers in Table 1. Thumbnail drawings of representative species by Michael Hanson.
FIG. 1 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 1. World map showing the collecting localities for specimens from which tissues were obtained for this study, along with the type locality for each species in the order. Specimen and type localities are most numerous in the western and southwestern Pacific, in the waters surrounding southern Africa, and on either side of the North Atlantic.
FIG. 4 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 4. Maximum parsimony (MP) phylogeny of Zeiformes based on morphological data analyzed in PAUP v.4b10 (Swofford, 2003). The data (Table 3) are a modified version of those used by Tyler and Santini (2005) but with revised outgroups reflecting zeiform membership in the Paracanthopterygii (e.g., Grande et al., 2013), and with character deletions, additions, and edits described in the text. The characters are listed in Appendix 1. This analysis is based on 27 terminal taxa and 105 characters, and resulted in a single shortest tree of 319 steps with CI 0.567. Support values at nodes are 1000-replicate bootstrap percentages/decay (Bremer) values. Character-state optimization was in MacClade 4.08 (Maddison and Maddison, 2005) using the ACCTRAN option as used also by Tyler et al. (2003) and Tyler and Santini (2005). Thumbnail drawings of representative species are original artwork by Michael Hanson.
FIG. 5 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 5. Comparison of branching patterns of morphological trees under maximum parsimony (MP) from three studies. Each family recognized by Tyler et al. (2003) is a different color. (A) Results from Tyler et al. (2003). (B) Results from Tyler and Santini (2005). (C) Results from the morphological analysis of the present study. Black lines in C indicate relationships with strong support; gray lines indicate weaker support. Note that the new tree resembles the previous trees but with the root moved to a position near Zeidae.
FIG. 2 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 2. Maximum likelihood (ML) phylogeny of the Zeiformes as reconstructed by Garli v2.0 (Zwickl, 2006), using sequence data for the eight molecular loci of Table 1, under the substitution models given in Table 2. Support values at nodes are bootstrap percentages. For details of the outgroup relationships see Figure 1S (see Data Accessibility). Asterisk (*) indicates sample originally cataloged as Cyttomimus affinis. Numbers after scientific names correspond to code numbers in Table 1.
FIG. 3 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 3. Bayesian inference (BI) phylogeny of the Zeiformes as reconstructed by MrBayes v.3.1.2 (Huelsenbeck and Ronquist, 2001; Ronquist and Huelsenbeck, 2003), using sequence data for the eight molecular loci of Table 1, under the substitution models given in Table 2. Support values at nodes are posterior probabilities. For details of the outgroup relationships see Figure 2S (see Data Accessibility). Asterisk (*) indicates sample originally cataloged as Cyttomimus affinis. Numbers after scientific names correspond to code numbers in Table 1.
Data from: Bajaichthys elegans from the Eocene of Bolca (Italy) and the overlooked morphological diversity of Zeiformes (Teleostei, Acanthomorpha)
Open the record for dataset details and reuse information.
FIG. 9 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 9. Morphometric analysis of 24 zeiform species for which combined molecular and morphological phylogenetic results were obtained as in Figure 7. (A) Thirteen landmarks used in the morphometric analysis shown on an image of Zenopsis nebulosa (CSIRO). (B–D) Wireframe diagrams in which the red wireframe represents an average form while the blue outline represents change in the direction of the principal component. (E) Phylomorphospace diagram showing variation in the morphospace defined by the first two principal components, with the combined phylogeny of Figure 7 mapped into the morphospace. Thin blue lines and thick black lines represent convergent lineages. Note that most of the major lineages arose from common ancestors with near-average morphologies (blue ellipse). Thumbnail drawings by Michael Hanson.
FIG. 6 in Phylogenetic Relationships among Fishes in the Order Zeiformes Based on Molecular and Morphological Data
FIG. 6. Combined (total-evidence) molecular and morphological phylogeny of the Paracanthopterygii based on Bayesian inference (BI) using MrBayes v.3.1.2 (Huelsenbeck and Ronquist, 2001; Ronquist and Huelsenbeck, 2003). See text for detailed methods and assumptions. Zeiform taxa with an asterisk (*) are those with morphological data only. Support values at nodes are posterior probabilities. For details within Zeiformes see Figure 7. Drawings of representative species by Michael Hanson.
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