Find research datasets worth reusing

FIGURE 3 in Systematic Revision Of The North American Syntropine Vaejovid Scorpion Genera Balsateres, Kuarapu, And Thorellius, With Descriptions Of Three New Species

FIGURE 3. Map of central Mexico, plotting known locality records for the vaejovid scorpion species, Thorellius tekuani, sp. nov. (triangles), and Thorellius wixarika, sp. nov. (circles), based on data collected in the present study.

FIGURE 31 in Systematic Revision Of The North American Syntropine Vaejovid Scorpion Genera Balsateres, Kuarapu, And Thorellius, With Descriptions Of Three New Species

FIGURE 31. Thorellius wixarika, sp. nov., habitus, dorsal (A, C) and ventral (B, D) aspects. A, B. Holotype ♂ (CNAN T01251). C, D. Paratype ♀ (AMNH). Scale bars = 5 mm.

FIGURE 30 in Systematic Revision Of The North American Syntropine Vaejovid Scorpion Genera Balsateres, Kuarapu, And Thorellius, With Descriptions Of Three New Species

FIGURE 30. Thorellius tekuani, sp. nov., holotype ♂ (CNAN T01250), dextral pedipalp chela. A. Dorsal aspect. B. Retrolateral aspect. C. Ventral aspect. D. Prolateral aspect. Scale bars = 1 mm.

FIGURE 1 in Systematic Revision Of The North American Syntropine Vaejovid Scorpion Genera Balsateres, Kuarapu, And Thorellius, With Descriptions Of Three New Species

FIGURE 1. Habitus in life. A. Balsateres cisnerosi (Ponce-Saavedra and Sissom, 2004), ♀; B. Kuarapu purhepecha Francke and Ponce-Saavedra, 2010, ♀; C. Thorellius cristimanus (Pocock, 1898), ♂; and D. Thorellius intrepidus (Thorell, 1876), ♀.

Fig. 30 in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 30. Male anterior thoracic sternum and pleon of Pseudosesarma. A, P edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; D, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; E, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; F, P. anteactum, paratype male (21.2 × 19.7 mm) (ZRC 2016.0603), Sri Lanka; G, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; H, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq.

Fig. 27 in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 27. Outer view of chela of Pseudosesarma. A, P. edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. edwardsii, male (19.4 × 17.3 mm) (ZRC 1971.9.24.8), Singapore; D, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; E, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; F, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; G, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; H, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq.

Fig. 37. A–G in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 37. A–G, Pseudosesarma brehieri, paratype female (14.9 × 13.4 mm) (ZRC 2016.0594), Myanmar; F, G, P. brehieri, male (15.0 × 13.6 mm) (ZRC 2013.0209), West Bengal, India; H, I, P. brehieri, male (14.5 × 13.0 mm) (ZRC 2013.0209), West Bengal, India; J–O, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq. A, K, male pleon; B, F, L, left G1 (ventral view, denuded); D, G, M, left G1 (dorsal view, denuded); E, left G2; H, O, left distal part of G1 (dorsal view, denuded); I, N, left distal part of G1 (ventral view, denuded); J, anterior thoracic sternites 1–4. Scales: A = 4.0 mm; B–E, N, O = 1.0 mm; F–I = 0.5 mm; J, K = 5.0 mm; L, M = 2.0 mm. A–E, after Ng (2018: fig. 7E–I).

Fig. 25 in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 25. Frontal view of cephalothorax of Pseudosesarma. A, P. edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; D, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; E, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; F, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; G, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq; H, Contusarma bocourti, male (25.3 × 23.3 mm) (ZRC 2000.0952), Bangkok, Thailand; I, Contusarma cheirogonum, neotype male (24.5 × 21.5 mm) (ZRC 1995.225), Bako National Park, Sarawak; J, Miersarma granosimanum, lectotype male (16.9 × 14.8 mm) (NHM 1880.6), Borneo.

Fig. 22. Overall habitus, Pseudosesarma species. A, P in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 22. Overall habitus, Pseudosesarma species. A, P. edwardsii, lectotype male (17.5 × 16.1 mm) (RMNH-D17a), Mergui Archipelago; B, P. edwardsii, male (13.4 × 11.9 mm) (ZRC 1965.8.2.81), Pulau Pawai, Singapore; C, P. edwardsii, male (12.9 × 11.8 mm) (ZRC 1971.9.24.9), Singapore; D, P. crassimanum, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore; E, P. anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; F, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India; G, P. brehieri, holotype male (17.4 × 15.7 mm) (ZRC 2016.0593), Myanmar; H, P. boulengeri, lectotype male (26.9 × 23.5 mm) (NHM 1919.11.14.1), Basra, Iraq.

Fig. 36. A–G in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species

Fig. 36. A–G, Pseudosesarma anteactum, holotype male (16.7 × 14.7 mm) (ZRC 2016.0602), Sri Lanka; H–L, P. glabrum, holotype male (13.8 × 12.0 mm) (CUSAT 2016-1), Kerala, India. A, I, left G1 (ventral view); B, J, left G1 (dorsal view); C, D, distal part of left G1 (ventral view, slightly different angles); E, K, ventro-mesial view of distal part of left G1; F, distal part of left G1 (dorsal view); G, L, left G2; H, pleon. Scales: A, B, G = 1.0 mm; C–F, I–L = 0.5 mm; H = 2.0 mm. A–G, after Ng & Schubart (2017: fig. 17); H–L, after Ng et al. (2017a: fig. 4).

Fig. 5 in Taxonomic status of genera of Buccininae (Neogastropoda, Buccinidae) updated based on molecular data with description of new species and corrections of nomenclature of Buccinum

Fig. 5. Buccinum bizikovi sp. nov. A–B. Holotype (ZIN 62781), SL 20.0 mm. C. Paratype (ZIN 62782), SL 20.0 mm, lateral view to show the penis. D. South-eastern Sakhalin, depth 78 m, SL 21.5 mm, ZIN 62783. E–F. Buccinum ovulum Dall, 1895 (ZIN 48103), Kurile Is, Iturup I., depth 605–620 m, SL 16.9 mm. G. Holotype (USNM 106997), Aleutian Is, Andreanof Is, Amukta Pass, depth 454 m, SL 25.6 mm. Photo G: courtesy of USNM.

Fig. 6 in Taxonomic status of genera of Buccininae (Neogastropoda, Buccinidae) updated based on molecular data with description of new species and corrections of nomenclature of Buccinum

Fig. 6. Buccinum hasegawai sp. nov. (A–C) and Buccinum bizikovi sp. nov. (D–F). A–B. Paratype (ZIN 62777), SL 16.5 mm. A. Radula. B. Operculum. C. Paratype (ZIN 62782), penis. D. Paratype (ZIN 62782), SL 16.5 mm, radula. E. Paratype (ZIN 62782), SL 19.1 mm, operculum. F. Paratype (ZIN 62782), SL 16.5 mm, penis. Scale bars: C, F = 1 mm.

Fig. 1 in Taxonomic status of genera of Buccininae (Neogastropoda, Buccinidae) updated based on molecular data with description of new species and corrections of nomenclature of Buccinum

Fig. 1. Part of the Bayesian phylogenetic tree of Buccinoidea Rafinesque, 1815 obtained with the cox- 1, 16S and 28S concatenated dataset representing family Buccinidae Rafinesque, 1815. The full tree is available as supplementary material (Supplementary file 1). Subfamily Siphonaliinae Finlay, 1928 is collapsed. Vertical numbered lines on the right mark the subfamilies of Buccinidae: 1 = Beringiinae Golikov & Starobogatov, 1975; 2 = Neptuneinae Stimpson, 1865; 3 = Volutopsinae Habe & Sato, 1973; 4 = Parancistrolepidinae Habe, 1972. Posterior probabilities and bootstrap values are shown for each medium supported node. Highly supported nodes are marked with black dots. The colors of the text refer to valid genus (orange = Volutharpa P. Fischer, 1856) and species referred to or morphologically attributable to formerly recognized (sub)genera of Buccininae: red = Thysanobuccinum Golikov & Gulbin in Golikov, 1980; blue = Ovulatibuccinum Golikov & Sirenko, 1988; green = Bathybuccinum Golikov & Sirenko, 1988.

Fig. 4 in Taxonomic status of genera of Buccininae (Neogastropoda, Buccinidae) updated based on molecular data with description of new species and corrections of nomenclature of Buccinum

Fig. 4. Buccinum hasegawai sp. nov. A–B. Holotype (ZIN 62775 (Buc274)), SL 18.5 mm. C. Paratype 1 (ZIN 62902 (Buc276)) from the type locality, SL 14.8 mm. D. Paratype 2 (MIMB 42300 (Buc273)), Urup I., 450–460 m, SL 14.7 mm. E. Paratype (ZIN 26228), Iturup I., 414 m, SL 16.1 mm. F. Paratype (ZIN 26228), Iturup I., 414 m, SL 16.2 mm, lateral view to show the penis. G. Buccinum bombycinum Dall, 1907 (ZIN 48100) Iturup I., 910–920 m, SL 15.3 mm. H–I. Syntype (USNM 1105311), Japan, Honshu I., Suruga Bay, 536 m, SL 23.9 mm. I = enlarged upper part of the shell to show the sculpture. Scale bars: A–H = same scale; I = 5 mm. Photos H–I: courtesy of USNM.

Fig. 2 in Taxonomic status of genera of Buccininae (Neogastropoda, Buccinidae) updated based on molecular data with description of new species and corrections of nomenclature of Buccinum

Fig. 2. Sequenced species of Buccinum Linnaeus, 1758 previously attributed to Thysanobuccinum Golikov & Gulbin in Golikov, 1980, Bathybuccinum Golikov & Sirenko, 1988 and Ovulatibuccinum Golikov & Sirenko, 1988. A–B. Buccinum tunicatum Golikov & Gulbin, 1977 (Buc265), Okhotsk Sea, off Urup I., depth 142 m, R/V Akademik Oparin, 56 cr., sta 7, SL 20.4 mm. C. Buccinum sp. 2 (Buc175), off Onagawa, Miyagi, Honshu I., Japan, depth 3302–3311 m, SL 20.3 mm. D–D'. Buccinum cf. tunicatum (Buc269), Okhotsk Sea coast of Urup I., 2 m, R/V Akademik Oparin, 56 cr., sta 26, SL 8.7 mm. D = at the same scale as others; D' = enlarged. E–E'. Buccinum bicordatum (Golikov & Sirenko, 1988) (Buc188), off Onagawa, Miyagi, Honshu I., Japan, depth 342–343 m, SL 8.4 mm. E = at the same scale as others; E' = enlarged. F. Buccinum unicordatum (Golikov & Sirenko, 1988) (Buc266), Kurile Is, Iturup I., Prostor Bay, depth 264–270 m, SL 15.9 mm. G. Buccinum chinoi nom. nov. (Buc190), off Onagawa, Miyagi, Honshu I., Japan, depth 342–343 m, SL 9.0 mm. H. Buccinum fimbriatum (Golikov & Sirenko, 1988) (Buc275), Kurile Is, Simushir I., depth 436 m, R/V Akademik Oparin, 56 cr., stn 19, SL 16.6 mm. I. Buccinum sp. 1 (Buc189), off Onagawa, Miyagi, Honshu I., Japan, depth 342–343 m, SL 22.4 mm. All shells (except D', E') at the same scale.

Fig. 3 in Taxonomic status of genera of Buccininae (Neogastropoda, Buccinidae) updated based on molecular data with description of new species and corrections of nomenclature of Buccinum

Fig. 3. Sequenced species of Buccinum Linnaeus, 1758, Volutharpa P. Fischer, 1856, and Plicibuccinum Golikov & Gulbin, 1977. A. Buccinum tenuisulcatum Golikov & Gulbin, 1977 (Buc264), Okhotsk Sea, Kurile Is, Onekotan I., depth 571–580 m, R/V Akademik Oparin, 56 cr., stn 68, SL 29.4 mm. B. Buccinum cyaneum Bruguière, 1789 (Buc281), Barents Sea, Teriberka Inlet, depth 10–17 m, SL 18.1 mm. C–D. Volutharpa ampullacea (Middendorff, 1848) (Buc277), Kurile Is, off Chirpoi I., depth 148–147 m, SL 14.1 mm. E. Buccinum nipponense Dall, 1907 (Buc187), off Otsuchi, Iwate, Honshu I., Japan, depth 479–484 m, SL 40.8 mm. F. Buccinum percrassum Dall, 1883 (Buc283), Kurile Is, Simushir I., 1–6 m, SL 33.5 mm. G–H. Buccinum cf. kobjakovae Golikov & Gulbin, 1977 (Buc278), Kurile Is, Simushir I., R/V Akademik Oparin, 56 cr., stn 19, 46°40.6′ N, 151°58.4′ E, depth 436 m, SL 12.1 mm. I. Plicibuccinum declivis (Habe & Ito, 1976) (Buc289), Japan Sea, Primorje, R/V Akademik Oparin, 64 cr., stn 73, 43°43.5′ N, 135°22.9′ E, depth 45–49 m, SL 36.2 mm. Shells not to scale.

Fig. 4 in Phylogenetic position of genera Acrostilicus Hubbard and Pachystilicus Casey (Staphylinidae, Paederinae) and their redescription

Fig. 4. Pachystilicus hanhami (Wickham, 1898), habitus photographs and drawings of the apical abdominal sternite and genital structures. A. Habitus, holotype, ♂ (NMNH). B. Habitus, additional male specimen with darker colouration (NMNH). C. Male sternite VIII. D. Aedeagus, parameral view. E. Aedeagus, lateral view. Scale bars = 0.5 mm.

Fig. 1. 50 in Phylogenetic position of genera Acrostilicus Hubbard and Pachystilicus Casey (Staphylinidae, Paederinae) and their redescription

Fig. 1. 50% majority-rule consensus tree from a Bayesian analysis of combined molecular and morphological datasets. Posterior probabilities (PP) and UFB values> 70 are shown near the corresponding nodes in PP/UFB format. A hyphen (-) refers to a lack of support in the result of certain analyses. Tribes and subtribes of Paederinae Fleming, 1821 are highlighted in colour.

Fig. 2. Acrostilicus hospes Hubbard, 1896 in Phylogenetic position of genera Acrostilicus Hubbard and Pachystilicus Casey (Staphylinidae, Paederinae) and their redescription

Fig. 2. Acrostilicus hospes Hubbard, 1896, habitus photograph and drawings of the apical abdominal sternite and genital structures. A. Habitus, lectotype, ♂ (NMNH). B. Male sternite VIII. C. Aedeagus, parameral view. D. Aedeagus, lateral view. Scale bar = 0.5 mm.

Fig. 3 in Phylogenetic position of genera Acrostilicus Hubbard and Pachystilicus Casey (Staphylinidae, Paederinae) and their redescription

Fig. 3. Pachystilicus quadriceps (LeConte, 1880), habitus photograph and drawings of the apical abdominal sternite and genital structures. A. Habitus, lectotype, ♂ (MCZ). B. Male sternite VIII. C. Aedeagus, parameral view. D. Aedeagus, lateral view. Scale bar = 0.5 mm.