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Fig. 2 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)

Fig. 2 Scanning electron microscopy images of a male specimen of Linguatula serrata (Frölich 1789) collected from Canis lupus (specimen number L4). A Anterior end of specimen, ventral view; ga, genital atrium. B Posterior hook with hook "pit" showing spines on wall (white box). C Spines on wall of hook "pit"

Fig. 5 in Molecular characterization and lesions associated with Diomedenema diomedeae (Aproctoidea: Desmidocercidae) from grey-headed albatrosses (Thalassarche chrysostoma) on Subantarctic Marion Island

Fig. 5. Bayesian phylogenetic tree of Diomedenema diomedeae based on COI gene sequences of spirurid worms. Branch lengths are drawn proportionally to evolutionary distance (scale bar is shown). Numbers adjacent to nodes indicate posterior probabilities.

Fig. 4 in Molecular characterization and lesions associated with Diomedenema diomedeae (Aproctoidea: Desmidocercidae) from grey-headed albatrosses (Thalassarche chrysostoma) on Subantarctic Marion Island

Fig. 4. Bayesian phylogenetic tree of Diomedenema diomedeae based on 18S rRNA gene sequences of spirurid worms. Branch lengths are drawn proportionally to evolutionary distance (scale bar is shown). Numbers adjacent to nodes indicate posterior probabilities.

Fig. 2 in Molecular characterization and lesions associated with Diomedenema diomedeae (Aproctoidea: Desmidocercidae) from grey-headed albatrosses (Thalassarche chrysostoma) on Subantarctic Marion Island

Fig. 2. Lesions associated with Diomedenema diomedeae infection in a grey-headed albatross chick (Thalassarche chrysostoma). Legend: (A) blood clots (arrows) and masses of pus (arrowheads) in the right thoracic air sac; (B) close-up of the blood clot and nematodes (arrowheads) in the right thoracic air sac; (C) nematodes (arrowheads) and masses of pus (arrows) in the abdominal air sacs; (D) tracheal hemorrhage.

Fig. 3 in Molecular characterization and lesions associated with Diomedenema diomedeae (Aproctoidea: Desmidocercidae) from grey-headed albatrosses (Thalassarche chrysostoma) on Subantarctic Marion Island

Fig. 3. Morphological characteristics of Diomedenema diomedeae. (A) Female, lateral view of the cephalic end: esophagus (e). (B) Female, dorsal view of the cephalic extremity: outer papilla (op), inner papilla (ip), vestibulum (ve), esophagus (e). (C) Male, lateral view of the posterior end (fast green counterstaining): large spicule (ls), small spicule (ss), precloacal papillae (pr). (D) Female, dorsal view of the cephalic end (fast green counterstaining): tricuspid tooth (tt), outer papilla (op), inner papilla (ip), vestibulum (ve). (E,F) Female, lateral view: uterus (u), vulva (v). (G,H) Eggs. Scale bars: (A) 125 μm, (B) 30 μm, (C) 150 μm, (D) 15 μm, (E) 100 μm, (F) 50 μm, (G,H) 30 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1. A in Molecular characterization and lesions associated with Diomedenema diomedeae (Aproctoidea: Desmidocercidae) from grey-headed albatrosses (Thalassarche chrysostoma) on Subantarctic Marion Island

Fig. 1. A grey-headed albatross (Thalassarche chrysostoma) chick at Greyheaded Albatross Ridge on Marion Island with drooping wings. A chick sitting with a normal posture can be seen in the background. Photo: P.G. Ryan.

Fig. 3 in Morphological and molecular characterization of Cystoisospora sp. from Asian small-clawed otters Aonyx cinereus

Fig. 3. Mid-point rooting tree of Cystoisospora spp. inferred from concatenated alignment of two nucleotide sequences (18S and cox1). Nucleotide sequences of Cystoisospora spp. GenBank/DDBJ/EMBL accession numbers for 18S and cox1 are shown next to species names. Nodal support values (NJ/ML) greater than 60% are represented on ML branches. Scale bar represents 0.01 nucleotide substitutions per sites.

Fig. 2 in Morphological and molecular characterization of Cystoisospora sp. from Asian small-clawed otters Aonyx cinereus

Fig. 2. Line drawing of sporulated oocysts of Cystoisospora rivolta-like oocysts from small-clawed otters. Bar = 10 μm.

Fig. 1 in Morphological and molecular characterization of Cystoisospora sp. from Asian small-clawed otters Aonyx cinereus

Fig. 1. Photographs of Cystoisospora oocysts detected from Asian small-clawed otters. (a and b) Immature oocysts containing one (a) or two sporoblasts (b). (c) Mature oocysts containing two sporocysts, each with four club-shaped sporozoites. Sporozoites contained rounded retractile vacuoles (arrow). (d–f) Sporozoites containing sporocyst residuum, which was composed of numerous small granules (d and e) or a rounded granule (f).

Fig. 1 in Molecular characterization and prevalence of Halarachne halichoeri in threatened southern sea otters (Enhydra lutris nereis)

Fig. 1. (A) Scanning electron microscopy of adult Halarachne halichoeri showing opisthosoma (abdomen) with slight constriction only at the anterior end and dorsal shield broader posteriorly than anteriorly with linguiform caudal tip. (B) Scanning electron microscopy of larvae Halarachne halichoeri with postanal setae (bristles) longer than adanal setae.

Fig. 3 in Isolation and characterization of unrecorded yeasts species in the family Metschnikowiaceae and Bulleribasidiaceae in Korea

Fig. 3. Phylogenetic tree derived from neighbor-joining analysis based on the D1/D2 domains of the LSU rRNA gene sequences, showing the placement of strains YP355, YP230 and YP366 in the genus Hannaella. Bulleromyces albus CBS 500T was used as outgroup. Bootstrap values of above 50% are given at nodes based on 1,000 replicates. Bar, 0.02 substitutions per site.

Fig. 2 in Isolation of wild yeasts from soils collected in Pochoen-si, Korea and characterization of unrecorded yeasts

Fig. 2. Neighbor-joining phylogenetic tree based on 26S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the genus Leucosporidium. Bar: 0.005 substitutions per site.

Fig. 2 in Isolation and characterization of unrecorded yeasts species in the family Metschnikowiaceae and Bulleribasidiaceae in Korea

Fig. 2. Phylogenetic tree derived from neighbor-joining analysis based on the D1/D2 domains of the LSU rRNA gene sequences, showing the placement of strain YI7 in the Kodamaea clade. Candida melibiosica CBS 5814T was used as outgroup. Bootstrap values of above 50% are given at nodes based on 1,000 replicates. Bar, 0.02 substitutions per site.

Fig. 1 in Isolation and characterization of unrecorded yeasts species in the family Metschnikowiaceae and Bulleribasidiaceae in Korea

Fig. 1. Photomicrographs showing budding cells of strains YI7 (a); YP355 (b); YP366 (c); YP320 (d). All strains were grown on YM agar for 3 days. Bars, 20 μm.

Fig. 1 in Isolation of wild yeasts from soils collected in Pochoen-si, Korea and characterization of unrecorded yeasts

Fig. 1. Phase-contrast micrographs of the unrecorded strains isolated in this study. Strains: A, YP204; B, YP205; C, YP211; D, YP215; E, YP189; F, YP196; G, YP329; H, YP76.

Fig. 3 in Isolation and characterization of unrecorded yeast species from Korea in the families Debaryomycetaceae and Piskurozymaceae

Fig. 3. Phylogenetic tree derived from neighbor-joining analysis based on the 26S rDNA gene sequences, showing the placement of strains 20g9-1 in the genus Solicoccozyma. Candida tropicalis ATCC 750T was used as outgroup. Bootstrap values of above 70% are given at nodes based on 1,000 replicates. Bar, 0.05 substitutions per site.

Fig. 2 in Isolation and characterization of unrecorded yeast species from Korea in the families Debaryomycetaceae and Piskurozymaceae

Fig. 2. Phylogenetic tree derived from neighbor-joining analysis based on the 26S rDNA gene sequences, showing the placement of strain YL1 in the Debaryomyces and YL9 in the Candida saitoana. Saitozyma paraflava CBS 10100T was used as outgroup. Bootstrap values of above 70% are given at nodes based on 1,000 replicates. Bar, 0.05 substitutions per site.

Fig. 1 in Isolation and characterization of unrecorded yeast species from Korea in the families Debaryomycetaceae and Piskurozymaceae

Fig. 1. Photomicrographs showing budding cells of strains YL1 (a), YL9 (b) and 20g9-1 (c). All strains were grown for 3 days on YM and YNB agar.

Fig. 4 in Characterizations of five heterotrophic nanoflagellates newly recorded in Korea

Fig. 4. (A, B) General light micrographs and sketch of Ancyromonas micra strain IG005. AF: anterior flagellum, PF: posterior flagellum, scale bar = 5 μm. Arrowhead and double arrowhead represent a shallow groove and rostrum, respectively. All micrographs are differential interference contrast (DIC) images. (C) Maximum likelihood phylogenetic tree inferred from the 18S rDNA sequences of Ancyromonadida (order) species including Ancyromonas micra strain IG005 and outgroup (Diacronema vlkiauum strain AC67 and Prymnesium patelliferum). Bootstrap support values (>70%) are shown at the nodes. Solid circles indicate a Bayesian posterior probability of 1 (posterior probability <0.75 not shown).

Fig. 3 in Characterizations of five heterotrophic nanoflagellates newly recorded in Korea

Fig. 3. (A, B) General light micrographs and sketch of Neobodo curvifilus (formerly Procryptobia sorokini) strain KM017. AF: anterior flagellum, PF: posterior flagellum, GR: granules, scale bar = 5 μm. All micrographs are differential interference contrast (DIC) images. (C) Maximum likelihood phylogenetic tree inferred from the 18S rDNA sequences of Neobodonida (order) species including Neobodo curvifilus strain KM017 and outgroup (Bodo saltans and Bodo uncinatus). Bootstrap support values (>80%) are shown at the nodes. Solid circles indicate a Bayesian posterior probability of 1 (posterior probability<0.95 not shown).