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Fig. 28 in Freshwater Stingrays Of The Green River Formation Of Wyoming (Early Eocene), With The Description Of A New Genus And Species And An Analysis Of Its Phylogenetic Relationships (Chondrichthyes: Myliobatiformes)

Fig. 28. †Heliobatis radians, AMNH P 19665, approximately 255 mm TL subadult (?) female, dorsally exposed (from F2 locality). Anterior to top.

Fig. 27 in Freshwater Stingrays Of The Green River Formation Of Wyoming (Early Eocene), With The Description Of A New Genus And Species And An Analysis Of Its Phylogenetic Relationships (Chondrichthyes: Myliobatiformes)

Fig. 27. Teeth of †Asterotrygon maloneyi, n.gen., n.sp. Occlusal (dorsal) (A), basal (B), lingual (C), labial (D), and lateral (E, F) views. Panels A–E from FMNH PF 12989 (paratype; adult male); panel F from FMNH PF 14069 (paratype; female). Teeth are obliquely positioned in order to facilitate comparisons (magnified 60×).

Fig. 20 in Freshwater Stingrays Of The Green River Formation Of Wyoming (Early Eocene), With The Description Of A New Genus And Species And An Analysis Of Its Phylogenetic Relationships (Chondrichthyes: Myliobatiformes)

Fig. 20. Enlarged view of FMNH PF 15180 from figure 12, depicting extremely wellpreserved jaws, ventral gill arches, and other features of a juvenile specimen of †Asterotrygon maloneyi, n.gen., n.sp. Note preservation of basihyal cartilage, first pair of hypobranchials, and gill rays of ventral pseudohyoid bar preserved in original positions.

Fig. 19 in Freshwater Stingrays Of The Green River Formation Of Wyoming (Early Eocene), With The Description Of A New Genus And Species And An Analysis Of Its Phylogenetic Relationships (Chondrichthyes: Myliobatiformes)

Fig. 19. Left aspect of neurocranium of †Asterotrygon maloneyi, n.gen., n.sp. (FMNH PF 14567; entire specimen in fig. 7), dorsally exposed, showing triangular shape of antorbital cartilage (indicated by arrowhead). Anterior to top.

Fig. 29 in Freshwater Stingrays Of The Green River Formation Of Wyoming (Early Eocene), With The Description Of A New Genus And Species And An Analysis Of Its Phylogenetic Relationships (Chondrichthyes: Myliobatiformes)

Fig. 29. †Heliobatis radians, FMNH PF 2020, approximately 463 mm TL adult male (terminal cartilages of claspers indicated by arrowhead), ventrally exposed (from F1 locality). Anterior to top.

Fig. 9 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 9. Close up of the polyps showing mantle vesicles in the examined taxa: A, Blastomussa merleti, New Caledonia, ST117; B, B. loyae, Djibouti; C, B. omanensis, Yemen; D, B. wellsi, New Caledonia, ST1084; E, B. vivida new species, New Caledonia, ST332; F, Nemenzophyllia turbida, Semporna, Malaysia; G, Physogyra lichtensteini, New Caledonia, ST1477; H, Plerogyra sinuosa, New Caledonia, ST1461. White arrows indicate mantle vesicle.

Fig. 1 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 1. Morphology of examined specimens, Blastomussa merleti: A, top and lateral view of typically phaceloid corallites (IRD HS3264); B, side view of a corallite of the same specimen; C, detail of a corallite (IRD HS1686). B. wellsi: D, corallite arrangement (IRD HS3011); E, side view of a corallite; F, columella of the same specimen. Morphology of examined specimens, B. loyae: G, cerioid corallites (UN- IMIB DJ050); H, lateral view of the colony surface showing exsert septa devoid of dentation in the same specimen as in G; I, detail of a corallite B. omanensis: J, polygonal corallites showing the typical "groove and tubercule" appearance (UNIMIB MU094); K, side view of the same specimen as in J; L, detail of a corallite. Morphology of examined specimens, B. vivida, new species: M) ceriod corallites of a paratype (RMNH Coel. 40091; same specimen as in Fig. 2D); N, side view of septa of specimen IRD HS3000; O, columella of the same specimen. Scale bars A, D, G, J, M = 1 cm; B, C, E, F, H, I, K, L, N, O = 5 mm. Numbers 1–6 in front of the septa in C, E, I, L, and M indicate their cycle number.

Fig. 5 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 5. Phylogenetic tree of rDNA (spanning the entire ITS1, 5.8S, ITS2 and a portion of 28S and 18S) reconstructed with Bayesian Inference. Numbers at each node show percentages of Bayesian posterior probability (>70%) and MP bootstrap (>50%); – = no support. Filled circles indicate well-supported clades (bootstrap values ≥99 and posterior probability of 100).

Fig. 8 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 8. In situ images of the examined taxa: A, Blastomussa merleti, New Caledonia, ST117; B, B. loyae, Djibouti; C, B. omanensis, Yemen; D, B. wellsi, New Caledonia, ST1084; E, B. vivida, new species, New Caledonia (IRD HS3000), ST332; F, Nemenzophyllia turbida, Semporna, Malaysia; G, Physogyra lichtensteini, New Caledonia, ST1477; H, Plerogyra sinuosa, New Caledonia, ST1461. Scale bars = 1 cm

Fig. 4 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 4. Phylogenetic tree of mitochondrial gene COI reconstructed with Bayesian Inference. Numbers at each node show percentages of Bayesian posterior probability (>70%) and MP bootstrap (>50%); – = no support. Filled circles indicate well-supported clades (bootstrap values ≥99 and posterior probability of 100).

Fig. 2 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 2. Blastomussa vivida, new species: A, the holotype (MNHN IK 2012 14226) (c1 and c2 are the larger and the smaller corallite, respectively); B, top view of corallite c1 of the same specimen, numbers 1–5 in front of the septa their cycle number; C, detail of the same corallite as in A and B showing the dentation and granulation of the septa; D, paratype (RMNH Coel. 40091); E, paratype (IRD HS3100); F, UBDM 6.0003; G, RMNH Coel. 40092; H, UBDM 6.0002. Scale bar = 1 cm

Fig. 3 in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 3. Blastomussa vivida, new species in situ: A, holotype (MNHN IK 2012 14226) from New Caledonia (same specimen as in Figs. 2A–C); B, specimen IRD HS3100 from New Caledonia; C, colony from Kota Kinabalu, Malaysia showing the typically fleshy and bright coloured polyps; D, the same colony as in C with partially retracted polyps showing cerioid arrangement; E, specimen RMNH Coel. 40092 from Brunei (same specimen as in Fig. 2G); F, from Cebu, the Philippines. Scale bars = 1 cm

Fig. 6. A in Phylogenetic relationships and revision of the genus Blastomussa (Cnidaria: Anthozoa: Scleractinia) with description of a new species

Fig. 6. A, Corallum; and B, detail of corallites of the holotype of Blastomussa omanensis (BMNH 1991.6.4.150) collected by C. Sheppard in Oman (Sheppard & Sheppard, 1991: Fig. 147); C, neotype of Parasimplastrea sheppardi (MTQ G 55860); and D, close up of corallites; E, paratype of Blastomussa loyae (ZMA 8322); and F, close up of its corallites. Scale bars A, C, E = 1 cm; B, D, F = 5 mm.

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Fig. 1 in Relationships Of Black-Fly Species Of The Simulium Tuberosum Species-Group (Diptera: Simuliidae) In Peninsular Malaysia, With Keys To Ten Malaysian Species

Fig. 1. The geographical distributions of 10 Malaysian species of the Simulium tubesrosum species-group. Numbers in circles correspond to the following species: 1, Simulium aeneifacies; 2, S. alberti; 3, S. brevipar; 4, S. jasmoni; 5, S. keningauense; 6, S. lunduense;7, S. masilauense; 8, S. sabahense; 9, S. tani;10, S. tiomanense. Dotted lines indicate international boundaries.

FIG. 4 in Description and Phylogenetic Relationships of a New Genus and Species of Lizard (Squamata, Gymnophthalmidae) from the Amazonian Rainforest of Northern Brazil

FIG. 4. Intergeneric variation of cloacal plate scales and precloacal pores: A, Marinussaurus curupira, INPA 19856; B, Arthrosaura reticulata, MPEG 19181; C, Colobosauroides cearensis, uncatalogued specimen from MPEG; D, Dryadosaura nordestina, MPEG 27738; E, Amapasaurus tetradactylus, MPEG 27370; F, Alopoglossus angulatus, MPEG 24372, a basal Gymnophthalmidae.

FIG. 3. Marinussaurus curupira, INPA 19856 in Description and Phylogenetic Relationships of a New Genus and Species of Lizard (Squamata, Gymnophthalmidae) from the Amazonian Rainforest of Northern Brazil

FIG. 3. Marinussaurus curupira, INPA 19856 (paratype). Drawing of the pericloacal region showing cloacal plate, precloacal and femoral pores. Scale bar = 5 mm.

FIG. 1 in Description and Phylogenetic Relationships of a New Genus and Species of Lizard (Squamata, Gymnophthalmidae) from the Amazonian Rainforest of Northern Brazil

FIG. 1. Marinussaurus curupira, in life, INPA 19856 (paratype). SVL = 56.2 mm. Photo by V.T. Carvalho.

FIG. 2. Marinussaurus curupira, INPA 19855 in Description and Phylogenetic Relationships of a New Genus and Species of Lizard (Squamata, Gymnophthalmidae) from the Amazonian Rainforest of Northern Brazil

FIG. 2. Marinussaurus curupira, INPA 19855 (holotype). Drawings of A, dorsal, B, lateral, and C, ventral views of the head. Scale bar = 5 mm.

FIG. 6 in Description and Phylogenetic Relationships of a New Genus and Species of Lizard (Squamata, Gymnophthalmidae) from the Amazonian Rainforest of Northern Brazil

FIG. 6. Phylogenetic trees inferred from parsimony (PAR) analyses. A, Strict consensus of three equally parsimonious trees from the analysis of the morphological characters, (L = 76, CI = 0.684, RI = 0.784). B, Single most parsimonious tree based on combined analyses of morphology and molecular partitions (L = 2634, CI = 0.525, RI = 0.481). Numbers above branches are bootstrap support values (BS) and numbers below branches are total Goodman-Bremer support values (GBS). Open diamonds represent Bayesian posterior probability values of 1.0 (PP; only shown for the Ecpleopodini clade). Node X represents incongruence among trees under PAR and Bayesian methods. Clades in node Y represent the tribe Ecpleopodini, sensu Pellegrino et al. (2001) and Rodrigues et al. (2005).