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Figure 27 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera

Figure 27. Varicus cephalocellatus, illustration of holotype, 28.2 mm SL, USNM 427232, based on notes of live coloration, by R.G. Gilmore.

Figure 21 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera

Figure 21. Psilotris laurae holotype, preserved, 26.8 mm SL, USNM 426779. Photo by J.L. Van Tassell.

Figure 8 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera

Figure 8. Ancestral character estimation for (A) branched versus unbranched 5th pelvic ray and (B) presence/absence of a well-developed membrane connecting the innermost pelvic rays. Pies at nodes represent posterior probabilities for ancestor's character state. Species from the eastern Pacific are denoted with "(P)".

Figure 26 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera

Figure 26. Varicus adamsi papillae pattern, composite from type series. Illustration by J.L. Van Tassell.

Figure 14. Pinnichthys saurimimica, holotype. 55.5 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera

Figure 14. Pinnichthys saurimimica, holotype. 55.5 mm SL, USNM 427228, in situ at 282 m, Bahamas, photo by R.G. Gilmore, from the Johnson Sea Link II submersible.

Figure 15. Pinnichthys saurimimica holotype, 55.4 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera

Figure 15. Pinnichthys saurimimica holotype, 55.4 mm SL, USNM 427228, preserved. Photo by J.L. Van Tassell.

FIGURE 6 in A new vole from Xizang, China and the molecular phylogeny of the genus Neodon (Cricetidae: Arvicolinae)

FIGURE 6. Maximum likelihood (ML) tree reconstructed from cytochrome b nucleotide sequences based on GTR + I + G model and rooted with Mesocricetus auratus. Bootstrap support above 50% is shown at nodes.

FIGURE 5. Fifty percent majority rule consensus tree from a in A new vole from Xizang, China and the molecular phylogeny of the genus Neodon (Cricetidae: Arvicolinae)

FIGURE 5. Fifty percent majority rule consensus tree from a Bayesian inference analysis of cytochrome b nucleotide sequences. Numbers at nodes represent posterior probabilities.

FIGURE 3 in A new vole from Xizang, China and the molecular phylogeny of the genus Neodon (Cricetidae: Arvicolinae)

FIGURE 3. Comparison of the glans penis of six voles (A: Neodon linzhiensis; B: N. sikimensis; C: N. irene; D: N. fuscus; E. N. leucurus). Numbered views are 1: glans; 2: midventral cut view; 3: urethral lappet; 4: dorsal papilla. For N. linzhiensis, lettered structural features are: a. distal baculum; b. outer crater; c. inner crater; d. ventral groove; e. glans; f. prepuce; g. penis body; h. station of dorsal papilla; i. lateral baculum (cartilage); j. urethral lappet; k. lateral baculum (bony part); l. distal baculum (bony part); and m. proximal baculum.

FIGURE 2 in A new vole from Xizang, China and the molecular phylogeny of the genus Neodon (Cricetidae: Arvicolinae)

FIGURE 2. Skull of the new species Neodon linzhiensis (A1: ventral view; A2: dorsal view; A3: lateral view; A4: lower jaw (ventral); A5: lower jaw (lateral)), and teethrows of five species of Neodon (B1, B2 and B3: N. linzhiensis; C1 and C2: N. sikimensis; D1 and D2: N. irene; E1 and E2: N. fuscus; F1 and F2: N. leucurus).

FIGURE 12 in A new interstitial species of the Hydroporus ferrugineus group from north-western Turkey, with a molecular phylogeny of the H. memnonius and related groups (Coleoptera: Dytiscidae: Hydroporinae)

FIGURE 12. Ultrametric tree obtained with Beast and an evolutionary rate of 0.0115 substitutions/site/MY for the H. memnonius, H. longulus and H. ferrugineus groups. Numbers in nodes, estimated ages; blue bars, 95% confidence intervals.

FIGURES 2–3 in A new interstitial species of the Hydroporus ferrugineus group from north-western Turkey, with a molecular phylogeny of the H. memnonius and related groups (Coleoptera: Dytiscidae: Hydroporinae)

FIGURES 2–3. Hydroporus bithynicus sp. n. (paratype male, DNA voucher specimen MNCN-AI782); 2) head and pronotum; 3) detail of the metacoxa (photos: A. Castro).

FIGURE 11 in A new interstitial species of the Hydroporus ferrugineus group from north-western Turkey, with a molecular phylogeny of the H. memnonius and related groups (Coleoptera: Dytiscidae: Hydroporinae)

FIGURE 11. Average node support (Bayesian posterior probability) (blue line) and number of species groups defined (red line) in each node level, counting from the root of the genus Hydroporus in the tree of Fig. 10.

FIGURES 7–9 in A new interstitial species of the Hydroporus ferrugineus group from north-western Turkey, with a molecular phylogeny of the H. memnonius and related groups (Coleoptera: Dytiscidae: Hydroporinae)

FIGURES 7–9. Habitat of Hydroporus bithynicus sp. n.; 7) detail of the spring in which all specimens were found; 8) general view of the stream between Yeniçaga and Mengen; 9) two of the authors (P. Aguilera and C. Hernando) next to the spring (photos: I. Ribera).

FIGURE 10 in A new interstitial species of the Hydroporus ferrugineus group from north-western Turkey, with a molecular phylogeny of the H. memnonius and related groups (Coleoptera: Dytiscidae: Hydroporinae)

FIGURE 10. Phylogram obtained with MrBayes. Above nodes, Bayesian posterior probabilities (when> 0.5) / bootstrap support values in Garli (when> 50%). "-", node not resolved; "x", node not present. See Table 1 for the localities and voucher reference of the specimens.

FIGURES 4–6 in A new interstitial species of the Hydroporus ferrugineus group from north-western Turkey, with a molecular phylogeny of the H. memnonius and related groups (Coleoptera: Dytiscidae: Hydroporinae)

FIGURES 4–6. Hydroporus bithynicus sp. n. (paratype male, DNA voucher specimen MNCN-AI782); 4) median lobe of the aedeagus, lateral view; 5) median lobe of the aedeagus, ventral view; 6) right paramere, lateral view. Scale bar: 1 mm (photos: A. Castro).

FIGURE 1 in Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China

FIGURE 1. Geographic location of sampling localities in Taiwan. Areas above 1000 m are shaded. Numerals refer to sampling sites mentioned in Table 1.

FIGURE 5 in Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China

FIGURE 5. Skulls of (a) Myotis laniger from Fujian, China (ZMB 4146, lectotype; hind parts missing), and (b) M. laniger from Taiwan (THUMB 103). Scale= 5 mm.

FIGURE 6 in Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China

FIGURE 6. Skulls of (a) M. secundus sp. n. from Taiwan (THUMB 92, paratype), (b) Myotis sowerbyi from Fujian, China (USNM 238869, holotype), (c) M. pruinosus from Japan (NSMT 14842, holotype), and (d) M. yanbarensis from Japan (NSMT 31306, holotype). Scale= 5 mm.

FIGURE 10. Gymnocorymbus bondi. a in Taxonomic revision and molecular phylogeny of Gymnocorymbus Eigenmann, 1908 (Teleostei, Characiformes, Characidae)

FIGURE 10. Gymnocorymbus bondi. a) Holotype of Phenacogaster bondi, ANSP 37863, 33.5 mm SL, Corisal, Río Orinoco basin, Venezuela; b) Holotype of Moenkhausia profunda, FMNH 53717, 39.0 mm SL, Guyana; c) Paratype of Gymnocorymbus socolofi, ANSP 139711, 26.1 mm SL, upper Río Meta, Río Orinoco basin, Colombia; d) Gymnocorymbus bondi, ANSP 191255, 59.5 mm SL, Río Ventuari, Río Orinoco basin, Venezuela. Photos by Kyle Luckenbill (a, c), ©Field Museum (b) and Mjaan McIvor (d).