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FIGURES 31–38. Servaea narraweena n in Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions

FIGURES 31–38. Servaea narraweena n. sp. 31–32 dorsal view (31 female, 32 male); 33–34 female genitalia (33 dorsal view of cleared specimen, 34 ventral view of external characteristics); 35–37 male palp (35 ventral view, 36 anterior lateral view, 37 posterior lateral view); 38 known and predicted distribution. Scale: total body 1 mm; remainder 0.2 mm.

FIGURE 2 in Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions

FIGURE 2. Observed and BIOCLIM predicted distributions of the genus Servaea based on all available specimens.

FIGURE 1 in Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions

FIGURE 1. Examples of intraspecific variation in abdomen patterning. A–D four specimens of S. villosa collected at the same location and showing similar COI sequences (Fig. 5); E–F dark and light forms of S. incana.

FIGURES 55–58. Servaea zabkai n in Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions

FIGURES 55–58. Servaea zabkai n. sp. 55 dorsal view (female); 55–57 female genitalia (56 dorsal view of cleared specimen, 57 ventral view of external characteristics); 58 known distribution. Scale: total body 1 mm; remainder 0.2 mm.

FIGURE 5 in Two new species of Siconema (Drilonematoidea: Ungellidae) parasitic in earthworms in Vietnam, and systematic relationships as inferred from ribosomal sequence data

FIGURE 5. Phylogram of the relationships between nematodes of the genera Siconema and Homungella tonkinense from Pu Mat National Park and other nematode genera based on the partial sequence of D2D3 expansion segment of LSU rDNA. A—Tree obtained with maximum parsimony and distance (NJ) optimality criteria. Number of bootstrap replicates = 10000; of 718 total characters: 276 characters are constant, 127 variable characters are parsimony-uninformative, number of parsimonyinformative characters = 315. Bootstrap values of MP and NJ analysis (in parentheses) are indicated near appropriate nodes. B—Maximum likelihood analysis, model selected - Model selected: GTR+G+I; – lnL = 6293.3618, Number of bootstrap replicates = 100, Bootstrap values are indicated near appropriate nodes.

FIGURE 4 in Two new species of Siconema (Drilonematoidea: Ungellidae) parasitic in earthworms in Vietnam, and systematic relationships as inferred from ribosomal sequence data

FIGURE 4. Siconema diducuncinum sp. n. SEM images. Female. A: hooks, dorsal view; B: stomatal tube, en face view; C: caudal organ, dorsal view; D: caudal organ, lateral view; E: margin of sub-lateral field. Scale bars in µm.

FIGURE 2 in Two new species of Siconema (Drilonematoidea: Ungellidae) parasitic in earthworms in Vietnam, and systematic relationships as inferred from ribosomal sequence data

FIGURE 2. Siconema ovicallosum sp. n. SEM images. Female. A, B: head hooks, latero-dorsal view; C: caudal organ, ventral view; D: amphid, lateral view. Scale bars in µm.

FIGURE 3 in Two new species of Siconema (Drilonematoidea: Ungellidae) parasitic in earthworms in Vietnam, and systematic relationships as inferred from ribosomal sequence data

FIGURE 3. Siconema diducuncinum sp. n. A & B, female & male in copula; C–H, female; I, J, male. C: pharynx region; C: posterior region; D: hooks; and G, I: hooks into D, G, I: hooks; J: posterior region. Except I, all in lateral position. Scale bars in µm.

FIGURE 1 in Two new species of Siconema (Drilonematoidea: Ungellidae) parasitic in earthworms in Vietnam, and systematic relationships as inferred from ribosomal sequence data

FIGURE 1. Siconema ovicallosum sp. n. A–G, female; H–K, male. A: entire worm; B: pharynx region; C: posterior region; D: vulval region; E: eggs; F: tail tip; G: hooks; H: entire worm; I: pharynx region; J: cloaca; K: caudal organ. All in lateral position. Scale bars in µm.

FIGURE 1. Bayesian phylogenetic tree inferred from SSU gene DNA sequences. Posterior probabilities great than 50 in New Zealand species of the genus Tripyla Bastian, 1865 (Nematoda: Triplonchida: Tripylidae). II: Two new, a known species and key to species

FIGURE 1. Bayesian phylogenetic tree inferred from SSU gene DNA sequences. Posterior probabilities great than 50% are given on appropriate clades. Nematode species, GenBank numbers, locations are listed for each taxon if known.

FIGURE 2 in The morphology and SSU rRNA gene sequence analysis of a poorly-known brackish water ciliate, Pinacocoleps tesselatus (Kahl, 1930) (Ciliophora, Colepidae) from Hangzhou Bay, China

FIGURE 2. Photomicrographs of Pinacocoleps tesselatus (Kahl, 1930) from live cells (A–G), after silver carbonate impregnation (H, J), and after protargol impregnation (I). (A) Lateral view of a typical individual. (B) Anterior secondary plate. (C) Anterior main plate. (D) Posterior main plate. (E) Posterior secondary plate. (F) A squashed specimen showing the arrangement of plates. (G) Posterior view, arrows mark the posterior spines. (H) Lateral view, arrows denote the oral basket, arrowheads mark the extrusomes. (I) Anterior view, showing the oral structure, arrows indicate the adoral organelles. (J) Lateral view, showing the ciliary pattern. Scale bars (in A, J) = 30 μm; in (B–H) = 10 μm.

FIGURE 1 in The morphology and SSU rRNA gene sequence analysis of a poorly-known brackish water ciliate, Pinacocoleps tesselatus (Kahl, 1930) (Ciliophora, Colepidae) from Hangzhou Bay, China

FIGURE 1. Morphology and infraciliature of Pinacocoleps tesselatus (Kahl, 1930) Foissner et al. 2008 (A–E), P. similis (Kahl, 1933) Chen et al. 2010 (F, G), P. heteracanthus (Noland, 1937) Chen et al. 2010 (H), P. arenarius (Bock, 1952) Chen et al. 2010 (I), P. spiralis (Noland, 1937) Chen et al. 2010 (J), P. i n c u r v u s (Ehrenberg, 1833) Foissner et al. 2008 (K), and P. pulcher (Spiegel, 1926) Foissner et al. 2008 (L). (A) Lateral view of typical individual. (B) One row of plates. The circumoral plate is omitted. (C) Ciliary pattern at apical end of body. (D) Ciliary pattern of P. t e s s e l a t u s. (E) P. tesselatus (Kahl, 1930) (from Kahl 1930). (F) P. similis (Kahl, 1933) (from Chen et al. 2010). (G) P. similis (Kahl, 1933) (from Borror 1972). (H) P. heteracanthus (Noland, 1937) (from Noland 1937). (I) P. arenarius (Bock, 1952) (from Bock 1952). (J) P. spiralis (Noland, 1937) (from Noland 1937). (K) P. i n c u r v u s (Ehrenberg, 1933) (from Kahl 1930). (L) P. pulcher (Spiegel, 1926) (from Kahl 1930). AO = adoral organelle; AS = anterior spine; CC = caudal cilium; CK = circumoral kinety; Ma = macronucleus; Mi = micronucleus; PC = perioral ciliature; PS = posterior spine; SK = somatic kinety. Scale bars = 30 μm.

FIGURE 3 in The morphology and SSU rRNA gene sequence analysis of a poorly-known brackish water ciliate, Pinacocoleps tesselatus (Kahl, 1930) (Ciliophora, Colepidae) from Hangzhou Bay, China

FIGURE 3. Maximum likelihood (ML) phylogenetic tree based on the small subunit (SSU) rDNA of Pinacocoleps tesselatus and other colepids. Numbers at branching points show bootstrap values of 1,000 replicates for ML tree and posterior probability for Bayesian (BI) tree, respectively. Fully supported (100%/1.00) branches are marked with solid circles. The scale bar corresponds to 10 substitutions per 100 nucleotide positions. Taxonomic classification mainly follows Lynn (2008). GenBank numbers follow species names.

FIGURE 7. Bayesian phylogenetic tree inferred from SSU rRNA gene sequences. Posterior probabilities greater than 50 in Description of Trischistoma abharensis n. sp. (Nematoda: Trischistomatidae) and first record of Tripylella intermedia (Bütschli, 1873) Brzeski & Winiszewska-Ślipinska, 1993 (Nematoda: Tripylidae) from Iran

FIGURE 7. Bayesian phylogenetic tree inferred from SSU rRNA gene sequences. Posterior probabilities greater than 50% are given on appropriate clades. Nematode species, GenBank accession numbers, and locations are listed for each taxon if known. The accession no. AY284737 was originally deposited in GenBank as Paratripyla sp., but it was used as Tripylella sp. by van Megen et. al. (2009).

FIGURE 10. Stenopsyche tienmushanensis Hwang 1957, larva. 10A–G in A new species of Stenopsyche, with descriptions of larvae and females of some species associated by gene sequences (Insecta: Trichoptera)

FIGURE 10. Stenopsyche tienmushanensis Hwang 1957, larva. 10A–G, head: 10A, dorsal; 10B, left lateral; 10C, ventral; 10D, labrum and clypeus, dorsal; 10E, mandibles, mentum, and anterior ventral apotome, ventral; 10F, left mandible, ventral; 10G, pair of #18 setae, posteroventral. 10H–I, prothorax: 10H, dorsal; 10I, left lateral. 10J–L, foreleg and propleuron: 10J, left foretrochantin, episternum, and epimeron, left lateroventral; 10K, left forecoxa, left lateral; 10L, right tarsus and claw, right lateral.

FIGURE 11 in A new species of Stenopsyche, with descriptions of larvae and females of some species associated by gene sequences (Insecta: Trichoptera)

FIGURE 11. Stenopsyche sp. 1, larva. 11A–F, head: 11A, dorsal; 11B, left lateral; 11C, ventral; 11D, labrum and clypeus, dorsal; 11E, mandibles, mentum, and anterior ventral apotome, ventral; 11F, left mandible, ventral, 11G, pair of #18 setae, posteroventral. 11H–I, prothorax: 11H, dorsal; 11I, left lateral. 11J-L, foreleg and propleuron: 11J, left foretrochantin, episternum, and epimeron, left lateroventral; 11K, left forecoxa, left lateral; 11L, right tarsus and claw, right lateral.

FIGURE 9. Stenopsyche tienmushanensis Hwang 1957, female genitalia. 9A in A new species of Stenopsyche, with descriptions of larvae and females of some species associated by gene sequences (Insecta: Trichoptera)

FIGURE 9. Stenopsyche tienmushanensis Hwang 1957, female genitalia. 9A, left lateral; 9B, dorsal; 9C, ventral.

FIGURE 8. Stenopsyche navasi Ulmer 1926, larva. 8A–F in A new species of Stenopsyche, with descriptions of larvae and females of some species associated by gene sequences (Insecta: Trichoptera)

FIGURE 8. Stenopsyche navasi Ulmer 1926, larva. 8A–F, head: 8A, dorsal; 8B, left lateral; 8C, ventral; 8D, labrum and clypeus, dorsal; 8E, mandibles, mentum, and anterior ventral apotome, ventral; 8F, left mandible, ventral; 8G, pair of #18 setae, posteroventral. 8H–I, prothorax: 8H, dorsal; 8I, left lateral. 8J–M, foreleg and propleuron: 8J, left foretrochantin, episternum, and epimeron, left lateroventral; 8K, left forecoxa, left lateral; 8L, right tarsus and claw, right lateral. 8M, left mesotrochanter, anterior.

FIGURE 7. Stenopsyche navasi Ulmer 1926, female genitalia. 7A in A new species of Stenopsyche, with descriptions of larvae and females of some species associated by gene sequences (Insecta: Trichoptera)

FIGURE 7. Stenopsyche navasi Ulmer 1926, female genitalia. 7A, left lateral; 7B, dorsal; 7C, ventral.

FIGURE 6. Stenopsyche angustata Martynov 1930, larva. 6A–F in A new species of Stenopsyche, with descriptions of larvae and females of some species associated by gene sequences (Insecta: Trichoptera)

FIGURE 6. Stenopsyche angustata Martynov 1930, larva. 6A–F, head: 6A, dorsal; 6B, left lateral; 6C, ventral; 6D, labrum and clypeus, dorsal; 6E, mandibles, mentum, and anterior ventral apotome, ventral; 6F, left mandible, ventral, 6G, pair of #18 setae, posteroventral. 6H–I, prothorax: 6H, dorsal; 6I, left lateral. 6J–L, foreleg and propleuron: 6J, left foretrochantin, episternum and epimeron, left lateroventral; 6K, left forecoxa, left lateral; 6L, right tarsus and claw, right lateral.