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opencc-by-4.0Apr 2015View details →

Fig. 1 in Endoparasites in a Norwegian moose (Alces alces) population - Faunal diversity, abundance and body condition

Fig. 1. Histogram of number of parasite groups (parasite diversity) found in individual moose (n = 30) shot during the licensed hunting season, autumn 2013, in Hedmark county, Norway.

Fig. 3 in Endoparasites in the feces of arctic foxes in a terrestrial ecosystem in Canada

Fig. 3. Phylogenetic tree showing relationship of Sarcocystis spp. detected in this study with existing reference sequence data in Genbank.

Fig. 1 in Endoparasites in the feces of arctic foxes in a terrestrial ecosystem in Canada

Fig. 1. Karrak Lake goose colony within the Queen Maud Gulf Bird Sanctuary, Nunavut. Inset map: sample collection sites within the goose colony.

Fig. 2. Melt curves for unknown samples. Each peak shows the melting temperature for a in Endoparasites in the feces of arctic foxes in a terrestrial ecosystem in Canada

Fig. 2. Melt curves for unknown samples. Each peak shows the melting temperature for a different coccidian species. Red: Sarcocystis (cervid), Blue: Neospora/Hammondia, Orange: Sarcocystis (avian), Black: Cystoisospora, Green: Eimeria sp., Pink: Eimeria sp. The horizontal axis indicates melting temperature (°C) and the vertical axis [—d(RFU)/dT] is related to the amount of DNA present.

Fig. 1. A in Endoparasites of the raccoon dog (Nyctereutes procyonoides) and the red fox (Vulpes vulpes) in Denmark 2009-2012 - A comparative study

Fig. 1. A map of Denmark showing the regions where the animals were sampled from 2009 to 2012. The grey shading indicates the mainland (Jutland), and the black shading the islands (Zealand, Funen, MØn, Lolland). Numbers above the bars are the sample sizes of each host species in each region.

opencc-by-4.0Dec 2016View details →

Fig. 1 in Endoparasites of American marten (Martes americana): Review of the literature and parasite survey of reintroduced American marten in Michigan

Fig. 1. Hookworm egg from an American marten (Martes americana). There was no significant difference in the prevalence of hookworm eggs in faecal samples from American marten from the Upper Peninsula (n = 18) and Northern Lower Peninsula (n = 31) of Michigan, USA (prevalence 11.1% and 16.1%, respectively). American marten infected with hookworms were significantly more likely to be anaemic than noninfected American marten (P = 0.01) with an odds ratio of 8.75 (95% confidence interval: 1.4‾56.4).

opencc-by-4.0Dec 2017View details →

Fig. 2 in Surrogate hosts: Hunting dogs and recolonizing grey wolves share their endoparasites

Fig. 2. Normalized helminth prevalence in hunting dogs from the wolf area (dark grey, n = 49) and control area without wolves (light grey, n = 29). Lack of statistical significance was determined using a GLM.

opencc-by-4.0Dec 2017View details →

Fig. 3. S. grueneri and S in Surrogate hosts: Hunting dogs and recolonizing grey wolves share their endoparasites

Fig. 3. S. grueneri and S. taeniata developmental cycles with their intermediate and definitive host in areas without wolves (A) and with wolves (B). In wolf habitats, wolves increase S. grueneri prevalence in their prey, in turn leading to a higher infection rate in hunting dogs. S. grueneri and S. taeniata strains spread by wolves are well‾adapted to both ungulate species, while S. grueneri and S. taeniata strains spread by hunting dogs from the control area are restricted to roe deer (right ungulate pictogram). The epidemiological influence of wolves regarding the spread of Sarcocystis in comparison to hunting dogs has a higher impact on red deer (left ungulate pictogram) than on roe deer. Sarcocystis strains in hunting dogs from the wolf area are likely to be a mixture of both dog and wolf strains. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

opencc-by-4.0Dec 2017View details →

Fig. 1 in Surrogate hosts: Hunting dogs and recolonizing grey wolves share their endoparasites

Fig. 1. Normalized Sarcocystis spp. prevalence in hunting dogs from the wolf area (dark grey, n = 49) and control area without wolves (light grey, n = 29). Hunting dogs were infected with 11 distinct Sarcocystis species, of which two species only occurred in wolf inhabited areas. They were significantly more likely to be infected with the 'wolf- ‾specialized' parasite S. grueneri when sharing their habitat with wolves (p = 0.035). It was not possible to determine a correlation for an infection with the other 'wolf specialist' S. taeniata and wolf presence (n.s. = not significant, p = 0.476). P values were extracted from GLMs.

Fig. 48 Partial Cytochrome Oxidase I sequences for 14 in Cryptic, adaptive radiation of endoparasitic snails: sibling species of Leptoconchus (Gastropoda: Coralliophilidae) in corals

Fig. 48 Partial Cytochrome Oxidase I sequences for 14 species of Leptoconchus; for each species, the respective combination of underlined nucleotides is considered diagnostic

Fig. 5 in Cryptic, adaptive radiation of endoparasitic snails: sibling species of Leptoconchus (Gastropoda: Coralliophilidae) in corals

Fig. 5 Transversional (solid circles) and transitional (open circles) rates in pairwise comparisons between COI sequences plotted against rates of all substitutions; rates calculated using Paup 4.0b10 (Swofford 2002)

Fig. 2 in Cryptic, adaptive radiation of endoparasitic snails: sibling species of Leptoconchus (Gastropoda: Coralliophilidae) in corals

Fig. 2 Map of Indo-Pacific region from Red Sea to Papua New Guinea, with research localities 1–10 (1= Egypt, Red Sea, Marsa Nakari c. 350 km S of Hurghada; 2 =Oman; 3=Maldives, Ari Atoll, Vilamendhoo Island; 4=Thailand, Krabi, PhiPhi Islands; 5=Palau; 6 =

Fig. 1 in Cryptic, adaptive radiation of endoparasitic snails: sibling species of Leptoconchus (Gastropoda: Coralliophilidae) in corals

Fig. 1 Leptoconchus snails inside of mushroom corals. a Coral broken to reveal gastropod endoparasites; arrow indicates snail about 2 cm in diameter. b Detail of upper surface of coral; arrow indicates snail's only opening to the outside world, a siphon extended through a 2–3 mm hole. c Detail of underside of coral; arrows indicate male left

opencc-by-4.0Apr 2018View details →

Fig. 3 in Occurrence of endoparasites in wild Antillean manatees (Trichechus manatus manatus) in Colombia

Fig. 3. The phylogenetic tree including the here identified trematodes Chiorchis fabaceus and Nudacotyle undicola shows that they belong to the superfamilies Paramphistomatoidea and Pronocephaloidea, respectively. Fasciola hepatica (Fasciolidae) was used as the outgroup taxon.

opencc-by-4.0Apr 2018View details →

Fig. 2 in Occurrence of endoparasites in wild Antillean manatees (Trichechus manatus manatus) in Colombia

Fig. 2. Illustrations of endoparasite stages identified in faecal samples of Antillean manatees (Trichechus manatus manatus) from Colombia: (A) Chiorchis fabaceus egg, (B) Eimeria manatus oocyst, (C) Eimeria nodulosa oocyst, (D) Nudacotyle undicola egg.

opencc-by-4.0Apr 2018View details →

Fig. 1. A in Occurrence of endoparasites in wild Antillean manatees (Trichechus manatus manatus) in Colombia

Fig. 1. A) Clinical evaluation of a calf manatee as part of the conservation programme of the OMACHA Foundation in Colombia. B) Blood collection for health status evaluation. C) 'Ciénaga Grande de Lorica', Cordoba, flowers of water spinach (Ipomea aquatica), are a favorite manatee food.

opencc-by-4.0Aug 2020View details →

Fig. 1. A in First report of Labrorostratus caribensis (Annelida, Oenonidae) as endoparasite of Haplosyllis rosenalessoae (Annelida, Syllidae) from Brazil

Fig. 1. A. Labrorostratus caribensis (parasite on the left) and Haplosyllis rosenalessoae (host on the right), lateral view; B. H. rosenalessoae, lateral view (* = enlarged region); C. L. caribensis, anterior region, lateral view; D. L. caribensis, lateral view; E. Mandibles and maxillae. (Scale bar: A, B, C, D: 0.5 mm; E: x400).

opencc-by-4.0Dec 2020View details →

Fig. 2 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species

Fig. 2. Parasites recovered from analyzed guignas in Chile: A-anterior extremity of female Molineus sp. (40x); B- caudal extremity of female Molineus sp. with caudal spine (40x); C- oral extremity of female Angiostrongylus sp. (40x); D-lateral view of caudal extremity of female Angiostrongylus sp. (40x); E-caudal extremity of male Angiostrongylus sp., caudal bursa and spicules can be observed (40x); F- lateral view of the rounded caudal extremity of female Oslerus sp. (40x); G-lateral view of the caudal extremity of male Oslerus sp., with characteristic short and stout spicules (40x); H- oral extremity of female Troglostrongylus sp. (100x); I- lateral view of the caudal extremity of male Troglostrongylus sp., long spicules and caudal bursa can be observed (40x).

opencc-by-4.0Dec 2020View details →

Fig. 3 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species

Fig. 3. Parasite richness (number of species/genera) in the analyzed guignas from Chile (a) overall, (b) by geographic zone and (c) by sex. Error bars represent standard error of 5%.