Find research datasets worth reusing

FIGURE 5. Balanodytes taiwanus Utinomi, 1950 in Acrothoracican barnacles (Lithoglyptida) in Taiwan, including the taxonomic status of Balanodytes taiwanus Utinomi, 1950 and cryptic diversity of Auritoglyptes bicornis (Aurivillius, 1892)

FIGURE 5. Balanodytes taiwanus Utinomi, 1950, mouth parts of female. (A) Maxillae. (B) Mandible. (C) Maxillule. (D) Mandibular palp. (E) Labrum. (F) Enlarged view distal edge of labrum from rectangle area on "E" showing fine teeth. Scale bars in Μm.

FIGURE 7 in Acrothoracican barnacles (Lithoglyptida) in Taiwan, including the taxonomic status of Balanodytes taiwanus Utinomi, 1950 and cryptic diversity of Auritoglyptes bicornis (Aurivillius, 1892)

FIGURE 7. Phylogenetic neighbor joining (NJ) tree of: (A) 16S and (B) Cytochrome oxidase subunit I (COI) region of lithoglyptid barnacles collected in present study, based on K2P genetic distance. The topologies of NJ and maximum likelihood (ML) trees are identical for 16S, and with inconsistency (dash line as ML tree) for COI. Bootstrap statistical significance was shown on the branches; those less than 50 were not indicated.

FIGURE 1 in Acrothoracican barnacles (Lithoglyptida) in Taiwan, including the taxonomic status of Balanodytes taiwanus Utinomi, 1950 and cryptic diversity of Auritoglyptes bicornis (Aurivillius, 1892)

FIGURE 1. (A) Syntype of Balanodytes taiwanus at Seto Marine Laboratory, Kyoto University, Japan. (B) Jar of the syntypes contains the base of a Megabalanus where found Balanodytes were removed, and a vial contained two dissected syntypes of B. taiwanus. (C) Opercular region of syntype of B. taiwanus with opercular bars and orificial knob magnified in (D) and posterior process magnified in (E). (F) A pairs of caudal appendages (ca, magnified in "G") were observed at the last pair of terminal cirri (tc). Abbreviations: ca—caudal appendages, tc—terminal cirri. Scale bars in Μm, except B in mm.

FIGURE 4. Balanodytes taiwanus Utinomi, 1950 in Acrothoracican barnacles (Lithoglyptida) in Taiwan, including the taxonomic status of Balanodytes taiwanus Utinomi, 1950 and cryptic diversity of Auritoglyptes bicornis (Aurivillius, 1892)

FIGURE 4. Balanodytes taiwanus Utinomi, 1950, terminal cirri and caudal appendages of female. (A) Posterior end of thorax with bases of terminal cirri and caudal appendages. (B) and (C) Caudal appendages, 2-segmented, without pedestal. (D) Terminal cirri and caudal appendages under scanning electron microscope (SEM), rear view. (E) and (F) Caudal appendages under SEM. (G) Rear view of terminal cirri under SEM. Abbreviations: ca—caudal appendages, tc1-4—terminal cirri, th— thorax. Scale bars in Μm.

FIGURE 6 in Acrothoracican barnacles (Lithoglyptida) in Taiwan, including the taxonomic status of Balanodytes taiwanus Utinomi, 1950 and cryptic diversity of Auritoglyptes bicornis (Aurivillius, 1892)

FIGURE 6. Auritoglyptes and Trypetesa from Taiwan. (A) Auritoglyptes bicornis (Aurivillius, 1892). Opercular bars of females from three genetic clades revealed from molecular analysis. (B) Trypetesa habei Utinomi, 1962 showing burrow opening and external view of female. Abbreviations: ob—opercular bar, obp—posterior process of opercular bar, ok—orificial knob, p—palps of mantle sac, sp—setose process of operculum (auricle). Scale bars in Μm.

FIGURE 3. Balanodytes taiwanus Utinomi, 1950 in Acrothoracican barnacles (Lithoglyptida) in Taiwan, including the taxonomic status of Balanodytes taiwanus Utinomi, 1950 and cryptic diversity of Auritoglyptes bicornis (Aurivillius, 1892)

FIGURE 3. Balanodytes taiwanus Utinomi, 1950, external morphology of female. (A) Lateral view of live female. (B) and (C) Posterior processes of opercular bars, opercular bars and orificial knob, showing variation in teeth number along the margin, lateral view. (D) and (E) Orificial knob, showing variation in teeth on surface, lateral view. (F) Opercular area observed under scanning electron microscope (SEM), upper lateral view. (G) Posterior process of opercular bars under SEM, showing teeth and setae, upper lateral view. (H) Orificial knob under SEM, showing teeth and sparse setae, upper view. (I) Comb collar under SEM, showing plumose projections. (J) Enlarged view of cuticular projections of comb collar. (K) Rows of massive multifid scales on opercular region. (L) Mantle teeth on surface of orificial knob. Abbreviations: cc—comb collar, ms—massive multifid scales, ob—opercular bar, obp—posterior process of opercular bar, ok—orificial knob. Scale bars in Μm.

FIGURE 6. Gastrotheca aratia. A in Cryptic species diversity in marsupial frogs (Anura: Hemiphractidae: Gastrotheca) in the Andes of northern Peru

FIGURE 6. Gastrotheca aratia. A, holotype, KU 212067 (holotype), adult female, 56.8 mm SVL, 8 km N Cutervo. B. KU 212055, male, 51.4 mm SVL, vicinity of Cutervo, Cajamarca, Peru.

FIGURE 4 in Cryptic species diversity in marsupial frogs (Anura: Hemiphractidae: Gastrotheca) in the Andes of northern Peru

FIGURE 4. Variation in dorsal color pattern among living adults of Gastrotheca aguaruna from the type locality, Molinopampa, Amazonas, Peru. A. KU 212021, male, 42.7 mm SVL. B. KU 212022, female, 50.8 mm SVL. C. KU 212024, male 43.3mm SVL. D. KU 212025, subadult, 36.8 mm SVL.

FIGURE 5 in Cryptic species diversity in marsupial frogs (Anura: Hemiphractidae: Gastrotheca) in the Andes of northern Peru

FIGURE 5. Topographic map of the Andean region of northern Peru showing localities of known occurrence of Gastrotheca aguaruna (black dots) and G. aratia (red dots), and names of political regions and major mountain ranges discussed in the text.

FIGURE 3 in Cryptic species diversity in marsupial frogs (Anura: Hemiphractidae: Gastrotheca) in the Andes of northern Peru

FIGURE 3. Dorsal and ventral coloration of preserved specimens of three species of Gastrotheca. A and D. G. monticola, KU 219771, 57.2 mm SVL, B and E. G. aguaruna, KU 212022, 50.8 mm SVL. C and F. G. aratia, KU 212067, 56.8 mm SVL.

FIGURE 2 in Cryptic species diversity in marsupial frogs (Anura: Hemiphractidae: Gastrotheca) in the Andes of northern Peru

FIGURE 2. Three previously described species of Gastrotheca from northern Peru. A–C. G. monticola: A. KU 219768, female, 62.1 mm SVL, from 1.8 km N Huancabamba, 1980 m, Piura, Peru; B. KU 219770, female, 60.2 mm SVL, from 4 km N Huancabamba, 1900 m, Piura, Peru; photos by E. R. Wild. C. MHNC 6742, male, 56.5 mm SVL, from Kuelap, 2920 m, Amazonas, Peru; photo by J. C. Chaparro. D. G. dysprosita, KU 212078, male, 60.5 mm SVL, from west slope Abra Barro Negro, 17 km (by road) WSW of Leimebamba, 3440 m, Amazonas, Peru; photo by W. E. Duellman. E and F. G. lateonota: E. KU 181730, female 62.1 mm SVL, KU 181732, female, 50.4 mm SVL, both from El Tambo, 2770 m, Piura, Peru; photos by W. E. Duellman.

FIGURE 1. A in Cryptic species diversity in marsupial frogs (Anura: Hemiphractidae: Gastrotheca) in the Andes of northern Peru

FIGURE 1. A postulated phylogenetic tree of selected species of Gastrotheca derived from a Maximum Likelihood analysis of four genes; the tree is rooted on Gastrotheca dendronastes (not shown). Node values indicate support based on proportion of 1000 bootstrap replicates.

FIGURES 9–12 in Sattleria revisited: unexpected cryptic diversity on the Balkan Peninsula and in the south-eastern Alps (Lepidoptera: Gelechiidae)

FIGURES 9–12. Male genitalia of Sattleria. 9, S. dinarica, sp. nov., paratype, slide GEL 1129; 10, S. triglavica Povolný, paratype, slide Mus. Vind. 11202; 11, S. haemusi, sp. nov., holotype, slide GU 13/1356 P. Huemer; 12, S. dzieduszyckii (Nowicki), slide L.M.P. 97.

FIGURE 21 in Sattleria revisited: unexpected cryptic diversity on the Balkan Peninsula and in the south-eastern Alps (Lepidoptera: Gelechiidae)

FIGURE 21. Neighbour joining tree of Sattleria from central and south-eastern Europe (Kimura 2 parameter, built with MEGA 5; cf. Tamura et al. 2011) based on sequences of the mtDNA COI gene (barcode fragment 5', 658 bp), except for S. basistrigella (599 bp, 1 specimen), S. dzieduszyckii (623 bp, 1 specimen), S. triglavica (540 bp, 1 specimen). Width of triangles represent sample size, depth the molecular variation within the cluster. Source: DNA Barcode data from BOLD (Barcode of Life Database, cf. Ratnasingham & Hebert 2007).

FIGURES 17–20 in Sattleria revisited: unexpected cryptic diversity on the Balkan Peninsula and in the south-eastern Alps (Lepidoptera: Gelechiidae)

FIGURES 17–20. Male genitalia of Sattleria, details of vincular processes (seconardy process marked with arrow) and valva. 17, S. dinarica, sp. nov., paratype, slide GEL 1129; 18, S. triglavica Povolný, paratype, slide Mus. Vind. 11202; 19, S. haemusi, sp. nov., holotype, slide GU 13/1356 P. Huemer; 20, S. dzieduszyckii (Nowicki), slide L.M.P. 97.

FIGURES 13–16 in Sattleria revisited: unexpected cryptic diversity on the Balkan Peninsula and in the south-eastern Alps (Lepidoptera: Gelechiidae)

FIGURES 13–16. Male genitalia of Sattleria, details of vincular processes (seconardy process marked with arrow) and valva. 13, S. sophiae, sp. nov., slide 1135 Timossi; 14, S. styriaca Pitkin & Sattler, slide 001 Wiesmair; 15, S. dolomitica, sp. nov., holotype, slide Mus. Vind. 1832; 16, S. basistrigella Huemer, slide GEL 1139.

FIGURES 5–8 in Sattleria revisited: unexpected cryptic diversity on the Balkan Peninsula and in the south-eastern Alps (Lepidoptera: Gelechiidae)

FIGURES 5–8. Male genitalia of Sattleria. 5, S. sophiae, sp. nov., slide 1135 Timossi; 6, S. styriaca Pitkin & Sattler, slide 001 Wiesmair; 7, S. dolomitica, sp. nov., holotype, slide Mus. Vind. 1832; 8, S. basistrigella Huemer, slide GEL 1139.

FIGURES 1–4 in Sattleria revisited: unexpected cryptic diversity on the Balkan Peninsula and in the south-eastern Alps (Lepidoptera: Gelechiidae)

FIGURES 1–4. Adults of Sattleria. 1, S. sophiae, sp. nov., holotype; 2, S. dolomitica, sp. nov., holotype; 3, S. dinarica, sp. nov., holotype; 4, S. haemusi, sp. nov., holotype.

FIGURE 42 in Diversity of sponges (Porifera) from cryptic habitats on the Belize barrier reef near Carrie Bow Cay

FIGURE 42. Smenospongia cf. echina, fiber skeleton (light microscopy): a, ectosomal reticulation ending in a conule; b, choanosomal reticulation, including primary fiber containing sediment particles; c, primary fiber with pith; d, primary fiber containing foreign (sedimentary) sponge spicules. Abbreviation: pf=primary fiber.

FIGURE 43 in Diversity of sponges (Porifera) from cryptic habitats on the Belize barrier reef near Carrie Bow Cay

FIGURE 43. Aplysina sciophila, anatomy/histology (holotype USNM1191343, light and electron microscopy): a, lightmicroscope view of fiber skeleton; b. SEM view of fiber cross-section, showing bark and pith; c. TEM view of choanocyte chamber, mesohyle full of bacteria, and spherulous cell; d. TEM view of bacteriocyte, spherulous cell, and mesohyle containing free bacteria. Abbreviations: ba=bacteria in mesohyle; bc=bacteriocyte; cc=choanocyte; sc=spherulous cell.