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Fig. 5 in Morphological and molecular studies on two myxosporean infections of cyprinid fishes: Thelohanellus pyriformis from tench and Thelohanellus cf. fuhrmanni from nase

Fig. 5. Phylogenetic tree generated by maximum likelihood analysis of ssrDNA sequences of Thelohanellus pyriformis and Thelohanellus fuhrmanni and other closely related myxozoan species identified by BLAST; GenBank accession numbers. Numbers at nodes indicate the bootstrap confidence values (ML). Chloromyxum cristatum was used as an outgroup.

Fig. 2 in Morphological and molecular studies on two myxosporean infections of cyprinid fishes: Thelohanellus pyriformis from tench and Thelohanellus cf. fuhrmanni from nase

Fig. 2. Spores of Thelohanellus pyriformis a) Schematic drawing of a spore in frontal view, b) Schematic drawing of a spore in sutural view. c) Microscopic photos of spores.

Fig. 4. a in Morphological and molecular studies on two myxosporean infections of cyprinid fishes: Thelohanellus pyriformis from tench and Thelohanellus cf. fuhrmanni from nase

Fig. 4. a) Plasmodia (p) of Thelohanellus cf. fuhrmanni enclosed in a cyst inside the loose connective tissue (ct) in the snout of the common nase. Empty holes (h) show the place of plasmodia fell out during histological processing or damaged by syringe at sampling spores b) Enlarged picture of T. cf. fuhrmanni plasmodia. Plasmodia are surrounded by a thin, dens connective tissue of the host (arrows) c) A part of T. cf. fuhrmanni plasmodium. Inside the connective tissue capsule (arrow) and the thin ectoplasm a dark staining layer of young developmental stages (white arrow) is located, followed by a zone of sporoblast (sb) and young spores (Yds) toward to the center. The center of the plasmodium is filled with matured spores (ms).

Fig. 1 in Morphological and molecular studies on two myxosporean infections of cyprinid fishes: Thelohanellus pyriformis from tench and Thelohanellus cf. fuhrmanni from nase

Fig. 1. Plasmodia (arrows) of Thelohanellus pyriformis in the lumen of arteria branchialis afferens (aa). Arteria branchialis efferens (ae) is uninfected. Histological section. H. and E. staining.

Fig. 3 in A tale of two nematodes: Climate mediates mustelid infection by nematodes across the geographical range

Fig. 3. Prediction of prevalence and infection intensity of Aonchotheca putorii and Molineus patens in the Northern Hemisphere based on averaged model estimates, using the WorldClim climate data set. Areas outside of the range of climatic variables used for model fitting are filled with checkerboard pattern. Transparency of the prediction colour reflects the coefficient of variation (CV) of predicted values (i.e. more uncertain prediction has more pattern tint). Predictions assumed the stomach was included in the analyses. (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 Role of three bird species in the life cycle of two Sarcocystis spp. (Apicomplexa, Sarcocystidae) in the Czech Republic

Fig. 2. Maximum likelihood tree for Sarcocystis halieti isolates from intermediate and definitive hosts (red asterisk) based on internal transcribed spacer sequences (HKY + I model). Sequences of the present study in blue. The tree was rooted on Sarcocystis arctica. (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 A tale of two nematodes: Climate mediates mustelid infection by nematodes across the geographical range

Fig. 1. Geographical location of study sites for the nematode parasites Aonchotheca putorii and Molineus patens, within the Palaearctic and Nearctic in seven mustelid host species. Details of the samples are given in Table S1.

Fig. 2 in A tale of two nematodes: Climate mediates mustelid infection by nematodes across the geographical range

Fig. 2. Model results for Aonchotheca putorii and Molineus patens infection parameters in seven mustelid species. Panels show model-averaged predictions of prevalence and infection intensity depending on the part of the alimentary tract analysed and climatic conditions (seasonality in precipitation and mean temperature of the warmest quarter). Points and lines show the mean, whiskers or shading denote 95% confidence intervals. Remaining explanatory variables were kept at their mean values or most common factor levels. The distribution of the data is shown at the bottom axes as a histogram or density plots.

Fig. 1 in Role of three bird species in the life cycle of two Sarcocystis spp. (Apicomplexa, Sarcocystidae) in the Czech Republic

Fig. 1. Sarcocystis halieti from Sturnus vulgaris. (a) Free thin-walled sarcocyst from skeletal muscle, wet mount. (b) Haematoxylin and eosin-stained histological sections of breast muscle with sarcocyst. Scale bars = 25 μm.

Fig. 5 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 5. The relationship between the prevalence of Eimeria spp. oocysts in European bison feces measured by the Willis and modified McMaster techniques (each point represents an individual parasite species).

Fig. 1 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 1. Probability of detection of Eimeria spp. oocysts with the modified McMaster technique based on the number of oocysts detected using the Willis technique.

Fig. 4 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 4. The relationship between the prevalence of various taxa eggs/oocysts in European bison feces measured by the Willis and modified McMaster techniques (each point represents an individual taxon/genus, blue points stand for oocysts and red point for eggs). (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 Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 3. Probability of detection of Trichostrongylidae eggs with the modified McMaster technique based on the number of eggs detected using the Willis technique.

Fig. 1 in Surveillance and genotype characterization of zoonotic trypanosomatidae in Didelphis marsupialis in two endemic sites of rural Panama

Fig. 1. Map showing the communities of Las Pavas (LP) (top set of images) and Trinidad de Las Minas (TM) (bottom set of images) with the number of opossums captured and infected with T. cruzi in the 3 collection sites in each community. A. Map with the geographic location of the LP and TM communities in the country of Panama. Satellite view of the P: Peridomicile (B), R1: remnant 1 (C) and R2: remnant 2 (D) collection site each with its 4 transects in the LP community. Satellite view of the P: Peridomicile (E), R1: remnant 1 (F) and R2: remnant 2 (G) collection site each with its 4 transects in the TM community.

Fig. 2 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 2. Probability of detection of Trichuris sp. eggs with the modified McMaster technique based on the number of eggs detected using the Willis technique.

Fig. 1. Myxobolus tihanyensis n in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 1. Myxobolus tihanyensis n. sp. plasmodia inhabiting Perca fluviatilis. (A). Plasmodia in the mesenchymal tissue between the caudal fin rays beneath the skin. (B) Plasmodia in the subcutaneous muscle close to the cartilage and ossified caudal fin rays (C) Plasmodia close to the pleural centrum (pc) located in the homocercal caudal fin. (D) Plasmodia is shown in the homocercal caudal skeleton in the urostyle (u) and the hypural (h). Note plasmodia are indicated in black arrows. Scale bars = 500 μm.

Fig. 4 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 4. Histology sections of Perca fluviatilis using the haematoxylin and eosin (H & E) technique. (A–B) Sagittal section of the proximal region of the caudal fin. (A) Rounded plasmodia (p) developing in the mesenchyme (mh) closely attached to the bases of the rays (r), scale bar = 100 μm. (B) Higher magnification of plasmodiacontaining spores. Scale bar = 20 μm. (C–D) Transversal section of the caudal vertebrate region. (C) Plasmodia located between the hemal spine (hs) and muscular fibres (mf), scale bar = 200 μm. (D) Higher magnification of plasmodia containing spores (black arrows), scale bar = 20 μm.

Fig. 3 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 3. Schematic drawings of the mature spore of Myxobolus tihanyensis n. sp. from the caudal fin of Perca fluviatilis (A) in frontal view, (B) in sutural view. Scale bar = 10 μm.

Fig. 2 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906

Fig. 2. Photomicrographs of Myxobolus tihanyensis n. sp. spores from Perca fluviatilis. (A–D) Myxobolus tihanyensis n. sp., and (E–H), Myxobolus sandrae from Sander lucioperca. (A, E) Numerous mature spores (s) illustrate an ovoid shape and two polar capsules (pc). (B, F) Ovoid spores with sutural markings (white arrows) with two polar capsules which contain coiled polar tubules (pf) (C, G) Spore in sutural view showing the suture (su) (D, H) Spores releasing the polar tubules (pf) and showing sutural markings. Figs. C, G and H represented spores stained with Lugol solution. Scale bars = 10 μm.

Fig. 4 in Surveys on Baylisascaris procyonis in two of the three French wild raccoon populations

Fig. 4. Results of the analysis of the population genetic structure of raccoon roundworms in north-western Europe. The three genetic clusters were inferred by the program BAPS, taking geographic coordinates into account. Different colors represent different genetic populations. Pie charts represent the genetic populations of origin of the individuals and their size is indicative of the number of samples included. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)