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Fig. 1 in Diversity of fecal parasitomes of wild carnivores inhabiting Korea, including zoonotic parasites and parasites of their prey animals, as revealed by 18S rRNA gene sequencing

Fig. 1. Diversity of fecal parasitomes of wild carnivores in Korea. The results shown are based on the diversity of zero-radius operational taxonomic units (ZOTUs) that were taxonomically assigned to parasites. (a) Comparison of richness and diversity of parasite ZOTUs between host animals estimated by the Chao1 estimator and Shannon index, respectively. (b) Non-metric multidimensional scaling (NMDS) plots showing the structure and membership of parasite ZOTUs represented by the Bray–Curtis dissimilarity and Jaccard index, respectively. In the panel (a), one asterisk (*) and two asterisks (**) represent p <0.05 and p <0.01, respectively, by the post hoc Wilcoxon rank-sum test. The abbreviation "ns" represents no statistical difference.

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Fig. 1 in Trichinella T9 in wild bears in Japan: Prevalence, species/genotype identification, and public health implications

Fig. 1. Map of Japan (A) illustrating the bear capture sites in this study (B). The red shapes indicate the capture sites for brown bears (Ursus arctos) and blue for Japanese black bears (Ursus thibetanus japonicus). The filled shapes indicate the locations of Trichinella-positive animals: A, Numata, Sorachi Subprefecture; B, Shimamaki, Shiribeshi Subprefecture; and C, Kaminokuni, Hiyama Subprefecture; D, Shiwa, Iwate Prefecture. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Molecular detection and characterization of Giardia spp., Cryptosporidium spp., and Blastocystis in captive wild animals rescued from central Colombia

Fig. 1. Cryptosporidium species in wild animals kept in captivity. The chord diagram shows the relation between Cryptosporidium species and the order and species of infected animals.

Fig. 5 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 5. Morphological comparison of Malayemys subtrijuga no. 5 between week 0 (A and B) and week 17 (C and D).

Fig. 4 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 4. Symptoms of Placobdelloides siamensis infection on Malayemys subtrijuga: (A) Leech penetration beneath the keratin layer (scute) on plastron from no. 8; (B) Shell holes resulting from leech penetration on plastron from no. 7; (C) Epidermal lesion on the hind foot from no. 6; (D) Keratin mandible jaw with leech consumption from no. 4.

Fig. 3 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 3. Trend analysis of red blood cell count (RCC) (left) and white blood cell count (WCC) (right) of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 1. Analysis of the mean red blood cell count (RCC) (blue line) and white blood cell count (WCC) (green line) of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 2. Analysis of the mean weight of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17).

Fig. 4 in New hosts for a snake's helminth: First report of intermediate and definitive hosts naturally infected by Ophidascaris arndti (Ascarididae) in the wild

Fig. 4. Scanning electron micrographs of Ophidascaris arndti larva from Akodon montensis. (A) Body; (B) Anterior end; (C) Apical view, amphids (am) and double papillae (dp); (D) Posterior end lateral view, anus (A).

Fig. 1 in Trichinella surveillance program in wild birds, Emilia-Romagna (northern Italy), 2006-2021. First report of Trichinella pseudospiralis in western marsh harrier (Circus aeruginosus) in Italy

Fig. 1. Alignment of homologous ESV sequences of T. pseudospiralis isolates belonging to Palearctic, Nearctic and Australian populations. C. aeruginosus, isolate from the western marsh harrier (ISS8343); IT_rk, isolate from a red kite (Milvus milvus) of the Basilicata region (ISS7768); IT_wb, isolate from a wild boar hunted in Northern Italy (ISS2851); FI, isolate from a raccoon dog (Nyctereutes procyonoides) of Finland (ISS681); SK, isolate from a peregrine falcon (Falcus peregrinus) of the Slovak Republic (MN963194); RU, isolate from a raccoon (Procyon lotor) of Southern Russia (ISS13); KZ, isolate from a tawny eagle (Aquila rapax) of Kazakhstan (ISS176); US, isolate from a black vulture (Coragypus atratus) of USA (ISS470); AU, isolate from a tiger cat (Dasyurus maculatus) of Australia (ISS141). Conserved bases are represented by dots; gaps are represented by dashes; different residues are highlighted in red; TGC microsatellite region is boxed in green. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Sarcoptic mange in wild ungulates in the European Alps - A systematic review

Fig. 1. Map of the European Alps and sarcoptic mange outbreaks in wild ungulates reported in the literature (n = 27). Host species is indicated with colour, the number of reported animals is indicated with size, and the time period is indicated by opacity. Grey area: alpine regions. Thin black lines: administrative boundaries. Thick black lines: country borders. The names of the countries are given. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in New hosts for a snake's helminth: First report of intermediate and definitive hosts naturally infected by Ophidascaris arndti (Ascarididae) in the wild

Fig. 3. Scanning electron micrographs of Ophidascaris arndti from Bothrops freitasi: (A) Male ventral view of the posterior end papillae (arrow); (B) Male cloaca (c) and papillae (arrow); (C) Male ventral view of tail, cloaca (c), papillae (arrow), and phasmid (ph, arrowhead); (D) Female ventro-lateral view of tail.

Fig. 2 in New hosts for a snake's helminth: First report of intermediate and definitive hosts naturally infected by Ophidascaris arndti (Ascarididae) in the wild

Fig. 2. Scanning electron micrographs of Ophidascaris arndti from Bothrops freitasi adult female. (A) Anterior end lateral view showing the excretory pore (arrow); (B) Dorsal view of lips, dorsal lip (D), double papillae (dp), lateroventral lips (LV), amphids (am), pointed depression (arrowhead); (C) Detail of denticles; (D) Detailed amphids.

Fig. 1 in New hosts for a snake's helminth: First report of intermediate and definitive hosts naturally infected by Ophidascaris arndti (Ascarididae) in the wild

Fig. 1. Light microscopy drawing of adult Ophidascaris arndti from Bothrops freitasi. (A) Female anterior end lateral view; (B) Female lips apical view; (C) Male posterior end lateral view, spicule, and ejaculatory duct; (D) Female posterior end ventral view; (E) Spicules; (F) Lateral view of the vulva, vagina, and uterine branches.

Fig. 2 in First detection and low prevalence of Pearsonema spp. in wild raccoons (Procyon lotor) from Central Europe

Fig. 2. Egg of Pearsonema spp. in urine sediment. The egg shows the characteristic features (barrel-shaped with bipolar plugs). Based on their morphology, the eggs were likely to be P. plica (see Discussion). Scale: 20 μm.

Fig. 1 in First detection and low prevalence of Pearsonema spp. in wild raccoons (Procyon lotor) from Central Europe

Fig. 1. Sampling areas, sample size (n) and prevalence of Pearonema spp. in wild raccoons (Procyon lotor) from Luxembourg, Poland and Germany. Luxembourg: LUX Luxembourg; Poland: ZL administrative district of Zgorzelecki; Germany: NH Northern Harzvorland, Saxony-Anhalt and administrative district of BZ Bautzen, Saxony; EIC Eichsfeld, Thuringia; PR Prignitz, Brandenburg; GO¨G¨oppingen, Baden-Württemberg.

Fig. 5 in New hosts for a snake's helminth: First report of intermediate and definitive hosts naturally infected by Ophidascaris arndti (Ascarididae) in the wild

Fig. 5. Photomicrography of Ophidascaris arndti larva from Akodon montensis. (A) Anterior end lateral view; (B) Posterior end lateral view.

Fig. 6 in New hosts for a snake's helminth: First report of intermediate and definitive hosts naturally infected by Ophidascaris arndti (Ascarididae) in the wild

Fig. 6. Phylogenetic relationships Bayesian tree based on partial MT-CO1 gene sequences of ascaridoid specimens, including Ophidascaris and outgroup. The numbers at the nodes are BPPs (left) and aLRT (right). The scale bar represents the number of substitutions per site.

Fig. 1 in Epidemiology of Trichinella infection in wild boar from Spain and its impact on human health during the period 2006-2019

Fig. 1. Prevalence of Trichinella infection in wild boar from several Spanish autonomous communities.

Fig. 4 in Epidemiology of Trichinella infection in wild boar from Spain and its impact on human health during the period 2006-2019

Fig. 4. Box-plot and post hoc pairwise comparison via Dunn's test of the incidence. Box-plot with different letters indicate a statistically significant difference.