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Figures 12–19 in Diversity and distribution of species of the planktonic dinoflagellate genus Alexandrium (Dinophyta) from the tropical and subtropical Mexican Pacific Ocean

Figures 12–19: Alexandrium globosum, LM. (12) Cell outline, with the central nucleus arrowed. (13, 14) Two different cells in ventro-lateral and ventral views, respectively, showing some plates of the epitheca and the sulcus. (15) Epitheca with plate tabulation, arrow indicates the location of the ventral pore in the first apical plate (1′). (16) Hypotheca showing plate tabulation. (17) Po plate. (18) Posterior sulcal plate (Sp). (19) Detail of some precingular, cingular and sulcal plates.

Figures 53–66 in Diversity and distribution of species of the planktonic dinoflagellate genus Alexandrium (Dinophyta) from the tropical and subtropical Mexican Pacific Ocean

Figures 53–66: Alexandrium tamiyavanichii, LM and SEM. (53) Chain of 6 cells,LM. (54) Detail of two cells with cellular content of a chain, LM. (55) Cells in ventral view showing the anterior sulcal plate (Sa), LM. (56) Two cells slightly twisted in a chain, SEM. (57) Cell in ventral view showing plates of the ventral area, LM. (58) Empty cell in ventral view showing plate tabulation, the ventral pore is arrowed, LM. (59) Epitheca in ventro-lateral view with plate tabulation, the left sulcal list is arrowed, SEM. (60, 61) Hypotheca with plate tabulation and pore at the posterior sulcal plate (Sp),SEM.(62, 63) Po and plates around it; the ventral pore is arrowed, LM. (64) Posterior sulcal plate (Sp) with pore (arrow), LM. (65, 66) Anterior sulcal plate, LM.

Figure 71 in Diversity and distribution of species of the planktonic dinoflagellate genus Alexandrium (Dinophyta) from the tropical and subtropical Mexican Pacific Ocean

Figure 71: Maximum-likelihood (ML) tree inferred from ITS sequences of Alexandrium. ML bootstrap and Bayesian posterior probabilities values are shown at branches. Bold letters indicate newly generated sequences in this study. Bootstrap values <50 and posterior probabilities <0.50 are not shown.

Figure 70 in Diversity and distribution of species of the planktonic dinoflagellate genus Alexandrium (Dinophyta) from the tropical and subtropical Mexican Pacific Ocean

Figure 70: Maximum-likelihood (ML) tree inferred from D1-D2 LSU rDNA sequences of Alexandrium. ML bootstrap and Bayesian posterior probabilities values are shown at branches. Bold letters indicate newly generated sequences in this study. Bootstrap values <50 and posterior probabilities <0.50 are not shown.

Fig. 5 in First Record of the Rare Parasitic Isopod Elthusa splendida (Cymothoidae) from the Pacific Ocean, Based on a Specimen Found in a Museum Shark Collection

Fig. 5. Map showing the distribution of Elthusa splendida. T and P indicate the type locality and the present specimen's locality, respectively.

Fig. 3 in First Record of the Rare Parasitic Isopod Elthusa splendida (Cymothoidae) from the Pacific Ocean, Based on a Specimen Found in a Museum Shark Collection

Fig. 3. Four pits on pereonite 1 of Elthusa splendida (HUMZ-C 2400, ovigerous female, 57.9 mm TL) from the buccal cavity of Japanese spurdog Squalus japonicus collected from the East China Sea. A, Photograph; B, three-dimensional digital scanned image.

Fig. 2 in First Record of the Rare Parasitic Isopod Elthusa splendida (Cymothoidae) from the Pacific Ocean, Based on a Specimen Found in a Museum Shark Collection

Fig. 2. Elthusa splendida (HUMZ-C 2400, ovigerous female, 57.9 mm TL) from the buccal cavity of Japanese spurdog Squalus japonicus collected from the East China Sea. A, Dorsal body; B, lateral body; C, ventral cephalon; D, ventral view of pleon; E, right pereopod 1; F, right pereopod 7; G–K, right pleopods 1–5 (pleopods 2, 4, 5 are partially damaged). Scale bars: 5 mm.

Fig. 4 in First Record of the Rare Parasitic Isopod Elthusa splendida (Cymothoidae) from the Pacific Ocean, Based on a Specimen Found in a Museum Shark Collection

Fig. 4. Morphological differences between Elthusa splendida (A) and E. raynaudii (B). Posterolateral angles of pereonite 7 (arrows) and relative width of pereonite 7 and pleotelson (dashed lines). Only body outlines are shown. Scale bars: 10 mm. A, HUMZ-C 2400, ovigerous female, 57.9 mm TL; B, MNHN-IU-2016-9885, syntype, ovigerous female, 26.7 mm TL.

Fig. 1 in First Record of the Rare Parasitic Isopod Elthusa splendida (Cymothoidae) from the Pacific Ocean, Based on a Specimen Found in a Museum Shark Collection

Fig. 1. Elthusa splendida (HUMZ-C 2400, ovigerous female, 57.9 mm TL) from the buccal cavity of Japanese spurdog Squalus japonicus collected from the East China Sea. A, Dorsal view; B, ventral view.

Fig. 8 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 8. Neighbor-joining tree based on sequence variations of the partial mitochondrial DNA COI gene. Sequences indicated by catalog numbers of specimens (shown by asterisks, determined here) or INSDC/BOLD registration numbers (determined in previous studies: see text). Numbers at branches indicate bootstrap probabilities following 1,000 bootstrap replications. Scale bar equals 0.02 of Tamura and Nei's (1993) distance.

Fig. 3 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 3. Preserved specimens of Canthidermis macrolepis. A, FAKU 38281, 266.9 mm SL, Shimane Prefecture, Japan; B, NSMT-P 23948, 276.2 mm SL, Micronesia; C, FAKU 131436, 298.3 mm SL, Hyogo Prefecture, Japan.

Fig. 1 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 1. Fresh specimens of Canthidermis macrolepis from Japan at different growth stages. A, OMNH-P 2297 (image cataloged as KPM-NR 3192), 206.9 mm SL, Hyogo Prefecture; B, NSMT-P 129777, 308.8 mm SL, Yamaguchi Prefecture; C, FAKU 135237, 330.0 mm SL, Kyoto Prefecture; D, FAKU 146571, 344.5 mm SL, Ishikawa Prefecture; E, KAUM–I. 115632, 317.2 mm SL, Kagoshima Prefecture. Photos (A, B and E) by T. Suzuki, NSMT and KAUM, respectively.

Fig. 4 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 4. Distributional map of Canthidermis macrolepis. Stars and circles indicate present and previous records, respectively. Closed and open stars indicate specimen- and photograph-based records, respectively.

Fig. 6 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 6. Fresh specimens of Canthidermis maculata from Japan at different growth stages. A, KAUM–I. 108293, 192.1 mm SL, Kagoshima Prefecture; B, OMNH-P 2298, 213.7 mm SL, Hyogo Prefecture (image catalogued as KPM-NR 3193); C, KAUM–I. 131240, 247.0 mm SL, Kagoshima Prefecture; D, KAUM–I. 55564, 262.7 mm SL, Kagoshima Prefecdture.

Fig. 5 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 5. Relationship between body depth at second dorsal-fin end (% SL) and standard length (mm) in Canthidermis macrolepis (stars) and C. maculata (triangles).

Fig. 2 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 2. Fresh specimen of Canthidermis macrolepis (53 cm TL; not retained) from Kusagaki Islands, Kagoshima Prefecture, Japan. Image cataloged as KAUM–II 71. Photo by J. Ohtomi.

Fig. 7 in First Specimen-based Records of Canthidermis macrolepis (Tetraodontiformes: Balistidae) from the Pacific Ocean and Comparisons with C. maculata

Fig. 7. Relationship between number of spinules per caudalpeduncle scale and standard length (mm) in Canthidermis macrolepis (stars) and C. maculata (triangles) (A); photographs of caudal peduncle scales in Japanese specimens of C. macrolepis, showing growth related changes (B, C). B, FAKU 38281, 266.9 mm SL; C, FAKU 135237, 330.0 mm SL. Bars indicate 5 mm.

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Fig. 1 in New Record of a Marine Fish Parasite Nerocila trichiura (Crustacea: Isopoda: Cymothoidae) from Japan, with its Confirmed Distribution in the Western North Pacific Ocean

Fig. 1. Nerocila trichiura, ovigerous female, NSMT-Cr 26315. A, Cypselurus hiraii (252 mm in total length) infested with N. trichiura (arrow); B, skin wound at attachment site; C, N. trichiura, dorsal view, fresh specimen. Scale bars: A, 50 mm; B, C, 10 mm.

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Fig. 2 in New Record of a Marine Fish Parasite Nerocila trichiura (Crustacea: Isopoda: Cymothoidae) from Japan, with its Confirmed Distribution in the Western North Pacific Ocean

Fig. 2. Nerocila trichiura, ovigerous female, NSMT-Cr 26315. A, dorsal view; B, lateral view; C, cephalon and pereonite 1, dorsal view; D, pleotelson and right uropod, dorsal view; E, pereopod 7. Scale bars: A, B, 10 mm; C, E, 2 mm; D, 5 mm.