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FIGURE 9 Hungarocypris suranareeae n in A checklist of Recent non-marine ostracods (Crustacea: Ostracoda) from Thailand, including descriptions of two new species

FIGURE 9 Hungarocypris suranareeae n. sp., male (MSU-ZOC.132). A. terminal part of penultimate segment and terminal segment of A2; B. right prehensile-palp, C. left prehensile-palp; D. hemipenis; E. Zenker organ. Scale bar = 100 Μm for B–D.

FIGURE 3 Dolerocypris sisaketensis n in A checklist of Recent non-marine ostracods (Crustacea: Ostracoda) from Thailand, including descriptions of two new species

FIGURE 3 Dolerocypris sisaketensis n. sp., female (MSU-ZOC.128). A. A1; B. A2; C. distal part of penultimate segment and terminal segment; D. Md-palp; E. terminal segment of Md-palp; F. Md-coxa. Scale bar = 100 Μm for A–B, F; 50 Μm for C–E.

FIGURE 2 Dolerocypris sisaketensis n in A checklist of Recent non-marine ostracods (Crustacea: Ostracoda) from Thailand, including descriptions of two new species

FIGURE 2 Dolerocypris sisaketensis n. sp., female. A. RV, internal view (MSU-ZOC.128); B. LV, internal view (ditto); C. anterior part of A; D. posterior part of A; E. posterior part of B; F. anterior part of B; G. carapace, left lateral view (MSU- ZOC.131); H. carapace, dorsal view (ditto). Scale bar = 500 Μm for A–B; 310 Μm for C–F; 230 Μm for G–H.

FIGURE 1 in A checklist of Recent non-marine ostracods (Crustacea: Ostracoda) from Thailand, including descriptions of two new species

FIGURE 1 Map of Thailand, showing the sampled provinces in each part of the country. Numbers refer to numbers of provinces in Table 1. ♠ Type locality of Dolerocypris sisaketensis n. sp., ★Type locality of Hungarocypris suranareeae n. sp.

FIGURE 5 Hungarocypris suranareeae n in A checklist of Recent non-marine ostracods (Crustacea: Ostracoda) from Thailand, including descriptions of two new species

FIGURE 5 Hungarocypris suranareeae n. sp., female (A, C–D, MSU-ZOC.135), male (B, E, MSU-ZOC.139). A. carapace, left lateral view; B. carapace, right lateral view; C. valve surface of A.; D. posterior part of A.; E. posterior part of B. Scale bar = 500 Μm for A–B; = 50 Μm for C; 100 Μm for D–E.

FIGURE 8 Hungarocypris suranareeae n in A checklist of Recent non-marine ostracods (Crustacea: Ostracoda) from Thailand, including descriptions of two new species

FIGURE 8 Hungarocypris suranareeae n. sp., female (MSU-ZOC.133). A. Mx1; B. T1; C. T2; D. T3; E. caudal ramus. Scale bar = 100 Μm for A–B; 200 Μm for C–E.

FIGURE 2 in Redescriptions of five species of marine peritrichs, Zoothamnium plumula, Zoothamnium nii, Zoothamnium wang, Pseudovorticella bidulphiae, and Pseudovorticella marina (Protista, Ciliophora)

FIGURE 2. Morphology of Zoothamnium nii and its synonyms from live cells (A, C–G, I–L, O, P, R), after staining with protargol (B, H, M, N), and after staining with silver nitrate (Q). A. General view of a typical zooid. B. Detail of infundibular polykineties. C, D. Zoothamnium duplicatum, after Kahl (1933). E, J. form of colony. F, G. Zoothamnium sp. after Kahl (1935). H. Oral view of the oral apparatus, arrow marks the epistomial membrane. I, K, L. Variations in shape of zooids. M. Lateral view showing macronucleus (dark area) and micronucleus (arrow). N. Macronucleus (dark area) and germinal kinety (arrow). O, P. Zooids at high magnification showing pellicuilar striations and variations in shape of the body. Q. General view of silverline system. R. Telotroch. Abbreviations: G, germinal kinety; H, haplokinety; P1–3, infundibular polykinety 1–3; Po, polykinety. Scale bars: 40 Μm (Figs. A, O, R), 50 Μm (Figs. L, P), 300 Μm (Figs. D–F, J, K).

FIGURE 5 in Redescriptions of five species of marine peritrichs, Zoothamnium plumula, Zoothamnium nii, Zoothamnium wang, Pseudovorticella bidulphiae, and Pseudovorticella marina (Protista, Ciliophora)

FIGURE 5. Morphology of Pseudovorticella marina (A–D, I–Q) and similar species (E–H). A, J, M. General view of typical cells. B. Variations in shape of the cell body. C. From Warren, 1986. D. Oral infraciliature, arrow marks the epistomial membrane. E. Pseudovorticella punctata (from Ji et al. 2006a). F. Vorticella campanulata (from Warren 1986). G. Vorticella fusca (from Warren 1986). H. Vorticella jaerae (from Precht 1935). I. Zooids seen at low magnification. K. Detail of stalk, arrows mark mitochondria. L. Detail of infundibular polykineties. N. Trochal band (arrows). O. Oral view of protargol impregnated specimen showing the epistomial membrane (arrow) and germinal kinety (arrowheads). P, Q. Silverline system, arrows mark pellicular pores. Abbreviations: G, germinal kinety; H, haplokinety; P1–3, infundibular polykinety 1–3; Po, polykinety. Scale bars: 20 Μm (Figs. A–C, E–H), 60 Μm (Fig. J), 100 Μm (Fig. M), 150 Μm (Fig. I).Fig. 1

FIGURE 4 in Redescriptions of five species of marine peritrichs, Zoothamnium plumula, Zoothamnium nii, Zoothamnium wang, Pseudovorticella bidulphiae, and Pseudovorticella marina (Protista, Ciliophora)

FIGURE 4. Morphology of Pseudovorticella bidulphiae (A–D, H–M) and similar species (E–G). A, I. General view of a typical cell. B. Variations in shape of the cell body. C, D. After Stiller (1939). E. Pseudovorticella pseudocampanula (after Foissner 1979). F. Pseudovorticella sauwaldensis (from Foissner and Schiffmann, 1979). G. Vorticella venusta (from Warren 1986). H. Oral infraciliature, arrow marks the epistomial membrane. J. Pellicular striations. K. Detail of stalk. L. Protargol-stained specimen showing infundibular polykineties. M. General view of silverline system, arrows mark the trochal band. Abbreviations: G, germinal kinety; H, plokinety; P1–3, infundibular polykinety 1–3; Po, polykinety. Scale bars: 20 Μm (Figs. A, E–G), 50 Μm (Figs. C, I).

FIGURE 3 in Redescriptions of five species of marine peritrichs, Zoothamnium plumula, Zoothamnium nii, Zoothamnium wang, Pseudovorticella bidulphiae, and Pseudovorticella marina (Protista, Ciliophora)

FIGURE 3. Morphology of Zoothamnium wangi from live cells (A, C, F–H, J), after staining with protargol (D, E, I, L, M), and after staining with silver nitrate (B, K). A. General view of a typical zooid. B, K. Silverline system, arrow marks the trochal band. C, F. Form of colony. D, M. Detail of infundibular polykineties. E. Oral infraciliature, arrow marks the epistomial membrane. G. Zooids at low magnification showing shape of the body. H. Highly magnified zooid showing pellicular striations. I. Lateral view showing macronucleus (dark area) and micronucleus (arrow). J. Structure of stalk showing densely arranged mitochondria in spasmoneme (arrow). L. Germinal kinety (arrow) and trochal band (arrowhead). Abbreviations: F, filamentous reticulum; G, germinal kinety; H, haplokinety; P1–3, infundibular polykinety 1–3; Po, polykinety. Scale bars: 5 Μm (Fig. J), 40 Μm (Fig. A), 50 Μm (Fig. G), 200 Μm (Fig. F), 250 Μm (Fig. C).

FIGURE 1 in Redescriptions of five species of marine peritrichs, Zoothamnium plumula, Zoothamnium nii, Zoothamnium wang, Pseudovorticella bidulphiae, and Pseudovorticella marina (Protista, Ciliophora)

FIGURE 1. Morphology of Zoothamnium plumula from live cells (A–F, J–M), after staining with protargol (H, I, N–P), and after staining with silver nitrate (G, Q) (A, G from Song et al. 2002; B, C after Kahl 1933). A. General view of a typical zooid. B, D–F. Different colony forms. C. Comparison of normal zooid with enlarged zooid. G. Silverline system, arrow marks the trochal band. H. Oral infraciliature, arrow marks the epistomial membrane, double-arrow indicates the distal fragment. I. Detail of infundibular polykineties. J. Branching pattern of a typical colony. K. Variations in shape of zooids. L. Detail of stalk, arrows mark mitochondria. M. Pellicular striations. N. Arrangement of infundibular polykineties. O. Germinal kinety (arrow) and radial myonemes in cell body (arrowheads). P. Epistomial membrane (arrow). Q. General view of silverline system. Abbreviations: G, germinal kinety; H, haplokinety; P1-3, infundibular polykinety 1–3; Po, polykinety. Scale bars: 30 Μm (Fig. A), 100 Μm (Fig. K), 400 Μm (Figs. F, J).

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FIGURE 2. A in A checklist of parasitic helminths reported from sixtyfive species of marine fish from Turkey including two new records of monogeneans

FIGURE 2. A photograph of Pyragraphorus pyragraphorus (Mac Callum and Mac Callum, 1913). Scale bar 1.1mm.

FIGURE 3 in The cane or marine toad, Rhinella marina (Anura, Bufonidae): two genetically and morphologically distinct species

FIGURE 3. Statistical parsimony network for the Rhinella marina species complex in northern Venezuela based on concatenated ND3+CR mitochondrial haplotypes. The left branches correspond to western populations and the right branches to eastern populations. Connections between haplotypes correspond to one mutational step and small dots indicate additional mutational steps.

FIGURE 4 in The cane or marine toad, Rhinella marina (Anura, Bufonidae): two genetically and morphologically distinct species

FIGURE 4. Trees showing phylogenetic relationships for the Rhinella marina species complex in northern Venezuela. Phylogenetic relationships are inferred from 429bp fragment of the ND3 (a) and 737bp for CR (b). The names refer to the location where the haplotype was collected and east and west to their location in relation the Andean Cordillera, as in Figure 1. The numbers at the nodes indicate maximum likelihood, maximum parsimony and Bayesian inference bootstrap values (ML/ MP/BI).

FIGURE 1 in The cane or marine toad, Rhinella marina (Anura, Bufonidae): two genetically and morphologically distinct species

FIGURE 1. Geographic distribution of Rhinella marina populations sampled for two mitochondrial markers and morphometric landmarks across the Andean cordillera in northern Venezuela. The circles indicate locations of specimens sequenced in this study and the squares indicate locations associated to previously published sequences used in this study. Black circles and squares correspond to eastern populations and white circles and squares to western populations. The geographic coordinates of localities are given in Table 1. The genetic distances between western and eastern populations (grey) are greater than between western populations (black) or between eastern populations (white) (see text for details).

FIGURE 2. Dorsal x in The cane or marine toad, Rhinella marina (Anura, Bufonidae): two genetically and morphologically distinct species

FIGURE 2. Dorsal x-ray images of Rhinella marina skulls from one western and one eastern population. Circles show the anatomical landmarks described in Table 2. The red circles correspond to landmarks showing the greatest contributions to the shape differences between eastern and western populations. The red arrows indicate the direction of displacement of landmarks. The white vertical bars indicate differences in measurements in externally visible landmarks between eastern and western populations.

FIGURE 5 in The cane or marine toad, Rhinella marina (Anura, Bufonidae): two genetically and morphologically distinct species

FIGURE 5. Morphological differences in skull shape between east and west populations of Rhinella marina. Changes with respect to the average on the deformation grids (a) and morphospaces in the canonical variates (b) resulting from comparisons between eastern and western populations.

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FIGURE 15 in Four new species of free-living marine nematodes of the family Desmodoridae (Nematoda: Desmodorida) and a redescription of Desmodora nini (Inglis, 1963) from the continental shelf off northeastern Brazil

FIGURE 15. Desmodora nini (Inglis, 1963) Female - A: overview. B: anterior region. C: head region. D: ovary and vulva opening. E: tail region.

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FIGURE 12 in Four new species of free-living marine nematodes of the family Desmodoridae (Nematoda: Desmodorida) and a redescription of Desmodora nini (Inglis, 1963) from the continental shelf off northeastern Brazil

FIGURE 12. Desmodora paraconica sp. n. Paratype female MNRJ 349 A: overview. B: anterior region. C: head region. D: ovary and vulva opening. E: tail region.