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Fig. 3 in Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica)

Fig. 3. Association between locomotor performance and pulmonary parasite intensity in Rhinella icterica (N = 20; r = –0.49, P = 0.03). SVL = snout-vent length.

Fig. 3 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 3. Single nucleotide polymorphisms in the ND2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Speciesspecific SNPs are shown in bold.

Fig. 1 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 1. Single nucleotide polymorphisms in the Cox1 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox1 gene (Franssen et al., 2013). Species-specific SNPs are shown in bold.

Fig. 2 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 2. Single nucleotide polymorphisms in the Cox2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox2 gene (Franssen et al., 2013).

Fig. 2 in Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica)

Fig. 2. Association between standard metabolic rate and total parasite intensity in Rhinella icterica (N = 22; r = –0.45, P = 0.03).

Fig. 1 in Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica)

Fig. 1. Association between the score of the first component of a PCA on morphological variables (large heart, kidney and intestine masses) and parasite intensities in Rhinella icterica (N = 16). Full circles represent total parasite intensity (r = 0.66, P <0.01), open circles represent pulmonary parasite intensity (r = 0.71, P <0.01), and open triangles represent intestinal parasite intensity (r = 0.51, P = 0.04).

Fig. 4 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 4. Single nucleotide polymorphisms in several tRNA genes of B. columnaris, compared to B. procyonis, B. transfuga and B. schroederi. Nucleotide position numbers are shown at the top of the figure. SNPs which distinguish B. columnaris from other Baylisascaris species are shown in bold.

Fig. 2 in Hepatozoon apri n. sp. (Adeleorina: Hepatozoidae) from the Japanese wild boar Sus scrofa leucomystax (Mammalia: Cetartiodactyla)

Fig. 2. Inflammatory lesion with released merozoites or gamonts in the femoral muscle of Japanese wild boar.

Fig. 1. a–b in Hepatozoon apri n. sp. (Adeleorina: Hepatozoidae) from the Japanese wild boar Sus scrofa leucomystax (Mammalia: Cetartiodactyla)

Fig. 1. a–b) Gamonts of Hepatozoon apri n. sp. in the cytoplasm of neutrophils detected in the blood smear of a boar (ID: 28-11), showing acentric and rounded nuclei (arrows) and a small protrusion containing eosinophilic granules (arrowheads).

Fig. 4 in Hepatozoon apri n. sp. (Adeleorina: Hepatozoidae) from the Japanese wild boar Sus scrofa leucomystax (Mammalia: Cetartiodactyla)

Fig. 4. Phylogenetic analysis of Hepatozoon apri n. sp. based on 18S rDNA sequences (522-bp). Adelina dimidiata (accession no. DQ096835) was chosen as the outgroup to root the phylogeny. Neighbor-joining (NJ) and maximum likelihood (ML) analysis showing the phylogenetic relationships among boar isolates and two Hepatozoon spp. (KF318170, KF318171) detected in Dermacentor ticks collected from wild boar in Thailand. Sequences included in the comparison were downloaded from the DDBJ/EMBL/GenBank databases. Filled circles indicate Hepatozoon species reported from Japan. Nodal support values based on 1000 bootstrap replicates (NJ/ML) are represented on the ML tree. Scale bar represents 0.01 nucleotide substitutions per site.

Fig. 3. a–d in Hepatozoon apri n. sp. (Adeleorina: Hepatozoidae) from the Japanese wild boar Sus scrofa leucomystax (Mammalia: Cetartiodactyla)

Fig. 3. a–d) Various developmental stages of Hepatozoon apri n. sp. detected in the muscles. a) A trophozoite (arrow) in the femoral muscles. The outer layer contains a fibroblast-like nucleus (arrowhead). b–c) Immature meronts found in the heart. d) Mature meront in the femoral muscles. H&E stain. Bar = 20 μm.

Fig. 2 in Occurrence of tongue worm, Linguatula cf. serrata (Pentastomida: Linguatulidae) in wild canids and livestock in south-eastern Australia

Fig. 2. In the petri dishes, adult males and females removed from the left and right nasal cavities of a wild dog; Right image shows the anterior end of a nymph removed from lymph node of a cow.

Fig. 1 in Occurrence of tongue worm, Linguatula cf. serrata (Pentastomida: Linguatulidae) in wild canids and livestock in south-eastern Australia

Fig. 1. Left: A female tongue worm being removed from the nasal cavity of a wild dog; Right: Two encapsulated tongue worm nymphs in a bovine mesenteric lymph node.

Fig. 4 in Occurrence of tongue worm, Linguatula cf. serrata (Pentastomida: Linguatulidae) in wild canids and livestock in south-eastern Australia

Fig. 4. Tongue worm eggs found in the faeces of a wild dog in the present study. Arrows indicate a pair of hooks.

Fig. 3. Localities where animals infected with L in Occurrence of tongue worm, Linguatula cf. serrata (Pentastomida: Linguatulidae) in wild canids and livestock in south-eastern Australia

Fig. 3. Localities where animals infected with L. cf. serrata were found. Open and solid symbols represent uninfected and infected animals, respectively. The stars, the red circles and the blue circles are cattle, wild dogs and foxes, respectively. Those animals that have been collected opportunistically have been excluded from this map. A) Creighton's Creek, B) Tallangatta, C) Mitta Mitta, D) Black Mountain, E) Corryong, F) Tumbarumba, G) Limestone, H) Wee Jasper, I) Brindabella, J) Mullion, K) Bullen Range, L) Booroomba, M) Perisher Valley, N) Orbost, O) Wabonga, P) Wangaratta, Q) Wodonga, R) Holbrook, S) Wagga Wagga, T) Towong, U) Braidwood, V) Carcoar. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 5 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 5. Transverse section of S. herzbergii skin parasitized by copepods. (Hematoxylineosin staining). a. Detail of the outer and middle layer of the epidermis (hyperplasia and hypertrophy) (100X). b. Sacciforme cell (400X).

Fig. 4 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 4. Cross section of healthy skin of S. herzbergii. Detail of the epidermis and dermis (staining with hematoxylin-eosin) (400X).

Fig. 2 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 2. Hemorrhagic cutaneous lesions caused by the infestation of copepods on S. herzbergii. a. Ventral view. b. Pectoral fins and mouth.

Fig. 3 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 3. Cross section of healthy skin of S. herzbergii, showing the different layers that make it up (Hematoxylin-eosin staining) (100X).