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Figure 7. A, Gronovius type specimens BMNH 53.11.12.49 in Delineating the fishes of the Clinus superciliosus species complex in southern African waters (Blennioidei: Clinidae: Clinini), with the validation of Clinus arborescens Gilchrist & Thompson, 1908 and Clinus ornatus Gilchrist & Thompson, 1908, and with descriptions of two new species
Figure 7. A, Gronovius type specimens BMNH 53.11.12.49, Clinus mycterizans, identified as Clinus superciliosus; B, BMNH 53.11.12.50, Clinus mycterizans, identified as Clinus cf. ornatus; C, BMNH 53.11.12.51, Clinus mycterizans, identified as Clinus superciliosus; D, BMNH 53.11.12.52, Clinus ignobilis, identified as Clinus acuminatus (Bloch & Schneider, 1801); E, MNHN 2143, Castelnau type specimen of Clinus marmoratus photograph; F, radiograph, identified as Clinus agilis Smith, 1931; G, Clinus superciliosus Linnaeus type NRM135a, photograph; H, radiograph.
Figure 4. A in Delineating the fishes of the Clinus superciliosus species complex in southern African waters (Blennioidei: Clinidae: Clinini), with the validation of Clinus arborescens Gilchrist & Thompson, 1908 and Clinus ornatus Gilchrist & Thompson, 1908, and with descriptions of two new species
Figure 4. A, Clinus ornatus, Lectotype, SAM MB-F038012, male, 158 mm SL (drawn by Elaine Heemstra); B, orbital cirri; C, D, Clinus ornatus underwater, False Bay (C, G. Zsilavecz; D, unknown); E, Clinus spatulatus, SAIAB 93658, male, 84.6 mm SL, Klein River estuary, aquarium photograph (W. Holleman); F, orbital cirri (from Bennett 1983); G, Clinus spatulatus underwater, male; H, female, Bot River estuary; I, female, Klein River estuary (G. Zsilavecz).
Figure 5 in Delineating the fishes of the Clinus superciliosus species complex in southern African waters (Blennioidei: Clinidae: Clinini), with the validation of Clinus arborescens Gilchrist & Thompson, 1908 and Clinus ornatus Gilchrist & Thompson, 1908, and with descriptions of two new species
Figure 5. Posterior of skull with first three dorsal-fin spines and supporting pterygiophores: A, Clinus superciliosus; B, Clinus ornatus.
Figure 3. A in Delineating the fishes of the Clinus superciliosus species complex in southern African waters (Blennioidei: Clinidae: Clinini), with the validation of Clinus arborescens Gilchrist & Thompson, 1908 and Clinus ornatus Gilchrist & Thompson, 1908, and with descriptions of two new species
Figure 3. A, Clinus musaicus, holotype, SAIAB 96616, male, 108 mm SL, Windmill, False Bay (drawn by Elaine Heemstra); B, orbital cirri; C, Clinus musaicus, photograph of holotype (G. Zsilavecz); D–F, Clinus musaicus underwater, habitat and different colour forms, False Bay (G. Zsilavecz).
Figure 6. A in Delineating the fishes of the Clinus superciliosus species complex in southern African waters (Blennioidei: Clinidae: Clinini), with the validation of Clinus arborescens Gilchrist & Thompson, 1908 and Clinus ornatus Gilchrist & Thompson, 1908, and with descriptions of two new species
Figure 6. A, Clinus superciliosus, SAIAB 8260, male, 78 mm SL (drawn by David Voorveld); B, orbital cirri; C–F, Clinus superciliosus underwater, different colour forms and habitats, False Bay; C is the 'default' colour form (G. Zsilavecz).
FIGURE 4 in Description of the second species of Synhalcurias Carlgren, 1914, Synhalcurias kahakui sp. nov. (Actiniaria: Actinernidae) with redescription of S. elegans (Wassilieff, 1908)
FIGURE 4. The cnidoms of Synhalcurias elegans and S. kahakui. A–L, cnidom of S. elegans. A–C, tentacle. A, spirocyst; B, basitrich; C, microbasic b-mastigophore. D–F, Actinopharynx. D, spirocyst; E, basitrich; F, microbasic p-mastigophore. G–I, Column. G, spirocyst; H, basitrich; I, microbasic p-mastigophore. J–M, filament. J, spirocyst; K, basitrich; L, microbasic p- mastigophore. M–Y, cnidom of S. kahakui. M–O, tentacle. M, spirocyst; N, basitrich; O, microbasic b-mastigophore. P–R, Actinopharynx. P, spirocyst; Q, basitrich; R, microbasic p-mastigophore. S–U, Column. S, spirocyst; T, basitrich; U, microbasic p- mastigophore. V–Y, filament. V, spirocyst; W, basitrich; X, microbasic b-mastigophore; Y, microbasic p-mastigophore (large).
FIGURE 2 in Description of the second species of Synhalcurias Carlgren, 1914, Synhalcurias kahakui sp. nov. (Actiniaria: Actinernidae) with redescription of S. elegans (Wassilieff, 1908)
FIGURE 2 Two syntypes of Synhalcurias elegans deposited in Bavarian State Collection of Zoology (ZSM). A, Lateral view of syntype (ZSM20040148, original Doflein's specimen no. 167); B, Lateral view of syntype (ZSM20040147, original Doflein's specimen no. 157A).
FIGURE 5 in Description of the second species of Synhalcurias Carlgren, 1914, Synhalcurias kahakui sp. nov. (Actiniaria: Actinernidae) with redescription of S. elegans (Wassilieff, 1908)
FIGURE 5. External and internal views of Synhalcurias kahakui sp. nov. (NSMT-Co 1695). A–C, External view. A, Whole living specimen of S. kahakui; B, oral view; C, preserved specimen. D–I internal view. D longitudinal section of tentacle; E, enlarged view of D; F, transverse section of tentacle; G, enlarged view of F; H. transverse section of actinopharynx; I, enlarged view of mesentery; J, transversal section of gamete (matured oocyte). Abbreviations: Ac, actinopharynx; Me, mesoglea; Oo, oocyte; Pm, parietal muscle; Rm, retractor muscle; Si, siphonoglyph; Te, tentacle. Scale bars: A–C, 1 cm; D, F, I, J, 200 µm; E, G, 50 µm; H, 1 mm.
FIGURE 3 in Description of the second species of Synhalcurias Carlgren, 1914, Synhalcurias kahakui sp. nov. (Actiniaria: Actinernidae) with redescription of S. elegans (Wassilieff, 1908)
FIGURE 3. External and internal views of Synhalcurias elegans (Wassilieff, 1908). A, B, F, G, NSMT-Co 1693; C–E, NSMT- Co 1694. A, B, external views of S. elegans. A, lateral view; B, oral view. C–H, internal views. C, gross section of upper column; D, transversal section of macrocnemes at upper column; E, transversal section of macrocnemes at lower column; F, longitudinal section of a tentacle; G, transversal section of a tentacle. Abbreviations: a, actinopharynx; fi, filament; go, gonad; ma, macrocneme; me, mesoglea; pa, parietal muscle; rm, retractor muscle; s, siphonoglyph; te, tentacle. Scale bars indicate 5 cm in A and B, 1 cm in C, 1 mm in D and E; F, G, 50 µm.
FIGURE 21. Koroga megalops Holmes, 1908 in A generic review of the lysianassoid family Uristidae and descriptions of new taxa from Australian waters (Crustacea, Amphipoda, Uristidae)
FIGURE 21. Koroga megalops Holmes, 1908, female, approx. 10.0 mm mm, AM P.69462; male A1 from male, 8.7 mm, AM P.69463, from east of Shoalhaven Heads, New South Wales, Australia. Scale bars: 0.1 mm.
FIGURE 9. Callorhynchocotyle amatoi. A. Whole mount. B in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 9. Callorhynchocotyle amatoi. A. Whole mount. B. Enlarged anterior section of whole mount. C. Enlarged mid-section of whole mount. Scale bars = 1000µm.
FIGURE 10 in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 10. Callorhynchocotyle amatoi sucker sclerites of complexes 1 (A), 2 (B) and 3 (C), and hamulus (D). Scale bars: A = 260µm, B, C = 340µm, D = 50µm.
FIGURE 11 in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 11. Callorhynchocotyle sagamiensis sucker sclerites of complexes 1 (A), 2 (B) and 3 (C), and hamulus (D). Scale bars: A, B, C = 360µm, D = 60µm.
FIGURE 8 in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 8. Callorhynchocotyle callorhynchi sucker sclerites of complexes 1 (A), 2 (B) and 3 (C), and hamulus (D). Scale bars: A = 260µm, B, C = 350µm, D = 60µm.
FIGURE 3. Hamulus morphological measurements. A in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 3. Hamulus morphological measurements. A. Rectangular grid, total length; line a–b, total diameter; line c–d; hook shank length; line e–f, hook point length; line f–g, distal hook point width; line f–h. B. Outer aperture angle (x) from vertex (f) by rays f–g, f–i, Root base angle (y) from vertex (j) by rays j–k, j–l. C. Inner aperture angle (z) from vertex (h) by rays h–g, h– i. Aperture; line g–i, hook shank base width; line e–i, outer root shaft length; line i–m, inner root shaft length; line i–n, root base width; line m–n. Abbreviations as for Fig. 1.
FIGURE 6 in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 6. Callorhynchocotyle marplatensis sucker sclerites of complexes 1 (A), 2 (B) and 3 (C), and hamulus (D). Scale bars: A = 260µm, B, C = 340µm, D = 60µm.
FIGURE 2. Hexabothriid sucker sclerite hook morphological measurements. A in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 2. Hexabothriid sucker sclerite hook morphological measurements. A. Hook length; line a–b, hook aperture; line b– c, hook base width; line a–c. B. Hook curve length; line e–f. C. Hook aperture angle (x) from vertex (f) by rays f–b, f–c.
FIGURE 1. Hexabothriid sucker sclerite morphological measurements. A in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 1. Hexabothriid sucker sclerite morphological measurements. A. rectangular grid (quad), circumference length (cir), total length; line a–b, total diameter; line c–d. B. Shaft width; line e–f; inner diameter; line f–g. C. Shaft length; line h–i. D. Aperture angle (x) from vertex (f) by rays f–j, f–k. E. Hook-side curve length; line l–m; shaft-side curve length; line n–o. F. Aperture; line j–k. Other abbreviations: gui, guide line.
FIGURE 5. Callorhynchocotyle marplatensis. A. Whole mount. B in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 5. Callorhynchocotyle marplatensis. A. Whole mount. B. Enlarged anterior section of whole mount. C. Enlarged mid-section of whole mount. Abbreviations: ao, anterior section of ovary; ap, appendix; ci, cirrus; dv, distal portion of vagina; eg, egg; ep, excretory pore; i, intestinal caecum; ivt, indentation of ventral tegument surrounding ovate distal cirrus; ji, junction of caeca posterior to testes; oot, ootype; os, oral sucker; p, pharynx; po, posterior section of ovary; sr, seminal receptacle; t, testes; vas, vas deferens; vd, vitteline duct; vp, vaginal pore; 1–3, sucker-sclerite complexes 1–3. Scale bars = 1000µm.
FIGURE 4 in Towards addressing the current state of confusion within the Hexabothriidae Price, 1942 (1908): Callorhynchocotyle Suriano & Incorvaia, 1982 (Monogenea: Hexabothriidae) re-visited, with the preliminary evaluation of novel parameters for measuring haptoral armature of hexabothriids
FIGURE 4. Principle Component Analysis plot (PCA) of all qualified character variables for the haptoral armature of all Callorhynchocotyle species excluding C. hydrolagi. Separations by component 1 are acted upon by decreasing sizes of the hamulus measurements and increasing sizes of sucker sclerites of all 3 sucker complexes. The function of the latter is likely to be influenced by the difference in sclerite symmetry of species parasitising representatives of Callorhynchidae and Chimaeridae. Separations by component 2 are acted upon significantly by sucker sclerites shape as a function of the relationship between length and diameter.
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