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FIGURE 10 in Myrmeleotettix Bolivar (Orthoptera, Gomphocerinae) in Anatolia on the basis of morphological and behavioural characters: data suggest a new species from southern end of the Anatolian refugium

FIGURE 10. Results of canonical discriminant function analysis using 5 song parameters (Durations of Phase I, Phase Ib and Phase II; Syllable periods of Phase Ib and Phase II).

FIGURE 3 in Anopheles (Kerteszia) lepidotus (Diptera: Culicidae), not the malaria vector we thought it was: Revised male and female morphology; larva, pupa, and male genitalia characters; and molecular verification

FIGURE 3. Anopheles (Kerteszia) lepidotus Zavortink, female habitus: A, wing; B, thorax, dorsal view; C, head, lateral view; D, thorax, lateral view; E, abdomen, dorsal and ventral views; F, (left to right) foreleg, anterior view; midleg, anterior view; hindleg, anterior view; hindleg, dorsal view.

FIGURE 1. The ITS2 in Anopheles (Kerteszia) lepidotus (Diptera: Culicidae), not the malaria vector we thought it was: Revised male and female morphology; larva, pupa, and male genitalia characters; and molecular verification

FIGURE 1. The ITS2 (rDNA) sequence alignments of Anopheles (Kerteszia) pholidotus (n = 3, Venezuela) and An. lepidotus (n = 5, Ecuador), using MAFFT (Katoh et al., 2002). A total of 343 nucleotides were identical; 45 transversions, 39 transitions, and 89 gaps were observed. Underlined bases show the ITS2 primers.

FIGURE 2 in Anopheles (Kerteszia) lepidotus (Diptera: Culicidae), not the malaria vector we thought it was: Revised male and female morphology; larva, pupa, and male genitalia characters; and molecular verification

FIGURE 2. Bootstrap NJ-K2P tree of COI sequences belonging to Anopheles (Kerteszia) lepidotus and An. pholidotus from Ecuador (EC) and Venezuela (VZ). Bootstrap values below 70 % are not shown. Outgroup: An. (Ker.) homunculus Komp.

FIGURE 4 in Anopheles (Kerteszia) lepidotus (Diptera: Culicidae), not the malaria vector we thought it was: Revised male and female morphology; larva, pupa, and male genitalia characters; and molecular verification

FIGURE 4. Anopheles (Kerteszia) lepidotus. A, male genitalia (from Zavortink, 1973); B, An. lepidotus pupal trumpet, pinna (Pi) long, about 0.5 trumpet length; C, pupal paddle showing lateral margin exceptionally thick, lateral margin without long filamentous spicules and relatively straight apical margin at 1-Pa; D, seta 3-C very thick and short; E, seta 6-VI stout, long, with median length aciculae on basal 0.33 and shorter aciculae more distal, without strong basal branches.

FIGURE 6 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters

FIGURE 6. Comparison of genitalia of Eufriesea zhangi sp. n. (left column) and E. nordestina Moure, 1999 (right column). A–B: ventral view of S7; C–D: ventral view of S8; E–F: lateral view of genital capsule; G–H: ventral view of genital capsule.

FIGURE 5 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters

FIGURE 5. Eufriesea nordestina (Moure, 1999). A: dorsal view of head and mesosoma; B: frontal view of face; C: dorsal view of metasoma; D: ventral view of mesotiba. E: frontal view of metatibia; F: metatibia seen from above.

FIGURE 4 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters

FIGURE 4. Holotype Eufriesea zhangi sp. n. A: dorsal view of head and mesosoma; B: frontal view of face; C: dorsal view of metasoma; D: ventral view of mesotiba. E: frontal view of metatibia; F: metatibia seen from above.

FIGURE 2 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters

FIGURE 2. Cluster of the 35 specimens (numbers 2 to 36) of Eufriesea nordestina (Moure, 1999) and the single specimen of Eufriesea zanghi sp. n. (number 1, right side) according to measurements of four morphological characters through SAS (see 'Material and Methods'). Each specimen is represented by numbers 1 to 36. The correspondent identification and access number at UFMG collection is shown in Appendix 1.

FIGURE 1 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters

FIGURE 1. Map illustrating northeastern Brazil and the type locality (black square) of Eufriesea zhangi sp. n. Acronyms represent Brazilian states, as following: AL: Alagoas; BA: Bahia; CE: Ceará; PB: Paraíba; PE: Pernambuco; PI: Piauí; RN: Rio Grande do Norte; SE: Sergipe.

FIGURE 3 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters

FIGURE 3. Tree constructed from the COI gene sequences using Maximum Likelihood (ML). An identical topology was obtained with Maximum Parsimony (MP), and bootstrap values for both reconstruction methods are shown above (ML) and below (MP) branches. The numbers shown in parentheses after the taxon names refer to the lineages and locations presented in Table 2. Exaerete smaragdina (Guérin-Méneville, 1844) was used as outgroup.

FIGURES 15–23. Morphological character variation within P. c a m b o u e i. Figs 15–17 in Revision of the Pachycondyla wasmannii - group (Hymenoptera: Formicidae) from the Malagasy region

FIGURES 15–23. Morphological character variation within P. c a m b o u e i. Figs 15–17: Head in profile showing the shape of the occipital corner. Fig. 15: Normally rounded in form 1; Fig. 16: Protruding as a lobe in form 2; Fig. 17: Hornlike extension in form 3. Figs 18–19: Mesosoma in lateral view showing hairs on propodeal dorsum. Fig. 18: Hairs present in form 1; Fig. 19: Hairs absent in form 4. Figs 20–21: Anterodorsal angles of pronotum. Fig. 20: Bidentate in form 5; Fig. 21: Smoothly rounded in form 6. Figs 22–23: Sculpture and pubescence on fourth abdominal tergite. Fig. 22: Smooth and shiny between large punctures and pubescence absent (form 1); Fig. 23: With closely-spaced small punctures between large punctures and abundant pubescence (form 6).

FIGURE 1 in Symphurus orientalis (Bleeker) redefined based on morphological and molecular characters (Pleuronectiformes: Cynoglossidae)

FIGURE 1. Symphurus orientalis (Bleeker, 1879), ASIZP 72344, female, 77.0 mm SL, off northeast Taiwan. A. Ocular-side pigmentation of freshly-caught specimen. B. Blind-side coloration of same specimen.

FIGURE 2. A in Symphurus orientalis (Bleeker) redefined based on morphological and molecular characters (Pleuronectiformes: Cynoglossidae)

FIGURE 2. A. Symphurus novemfasciatus Shen and Lin, 1984, holotype, NTUM 04586, female, 79.9 mm SL, off Dong-Gang, southwest Taiwan. B. Blind-side coloration of same specimen. C. Symphurus orientalis, Neotype, BSKU 44238, female, 91.0 mm SL, collected off Kochi, Japan. D. Blind-side coloration of Neotype.

FIGURE 5 in Symphurus orientalis (Bleeker) redefined based on morphological and molecular characters (Pleuronectiformes: Cynoglossidae)

FIGURE 5. Neighbor-joining tree (part) from partial COI gene sequence of species of Symphurus. Numbers above nodes indicate bootstrap value for 10000 replications.

FIGURE 4 in Symphurus orientalis (Bleeker) redefined based on morphological and molecular characters (Pleuronectiformes: Cynoglossidae)

FIGURE 4. Neighbor-joining tree (part) from partial 16S rRNA gene sequence of species of Symphurus. Numbers above nodes indicate bootstrap values for 10000 replications.

FIGURE 3 in Symphurus orientalis (Bleeker) redefined based on morphological and molecular characters (Pleuronectiformes: Cynoglossidae)

FIGURE 3. Geographic distribution of Symphurus orientalis based on specimens examined in this study (indicated by triangles) and reliable literature reports (indicated by stars). Questionable localities in the literature where S. orientalis has been reported to occur are indicated by a question mark (?). Symbols may represent more than one locality and/or more than a single collection from each locality.

FIGURE 1. Lauriea adusta n in A new genus and some new species of the genus Lauriea Baba, 1971 (Crustacea, Decapoda, Galatheidae) from the Pacific and Indian Oceans, using molecular and morphological characters

FIGURE 1. Lauriea adusta n. sp., holotype, ovigerous female, 3.3 mm, Philippines, PANGLAO, Stn B19 (NTUO). A, carapace and abdomen, dorsal view; B, sternal plastron, sternites 3 and 4; C, left cephalic region, showing antennular and antennal peduncles, ventral view; D, right Mxp3, lateral view; E, right P1, dorsal view; F, right P2, lateral view; G, right P3, lateral view; H, right P4, lateral view. Scale: A, E–H = 1 mm; B–D = 0.5 mm.

FIGURE 6. Lauriea teresae n in A new genus and some new species of the genus Lauriea Baba, 1971 (Crustacea, Decapoda, Galatheidae) from the Pacific and Indian Oceans, using molecular and morphological characters

FIGURE 6. Lauriea teresae n. sp., holotype, ovigerous female, 2.7 mm, French Polynesia, Moorea Island (UF-10148). A, carapace and abdomen, dorsal view; B, sternal plastron, sternites 3 and 4; C, left cephalic region, showing antennular and antennal peduncles, ventral view; D, right Mxp3, lateral view; E, right P1, dorsal view; F, left P2, lateral view; G, left P3, lateral view; H, left P4, lateral view. Scale: A, B–H = 1 mm; C–D = 0.5 mm.

FIGURE 5. Lauriea simulata n in A new genus and some new species of the genus Lauriea Baba, 1971 (Crustacea, Decapoda, Galatheidae) from the Pacific and Indian Oceans, using molecular and morphological characters

FIGURE 5. Lauriea simulata n. sp., holotype, ovigerous female, 2.7 mm, Vanuatu, SANTO, Stn FR4-F22 (MNHN-IU-2010- 5290). A, carapace and abdomen, dorsal view; B, sternal plastron, sternites 3 and 4; C, left cephalic region, showing antennular and antennal peduncles, ventral view; D, right Mxp3, lateral view; E, right P1, dorsal view; F, right P2, lateral view; G, right P3, lateral view; H, right P4, lateral view. Scale: A, B, E–H = 1 mm; C–D = 0.7 mm.