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280 results for “endoparasite”
Fig. 6 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. 6. Distribution of parasite infection intensity (total number of helminths per guigna) in the analyzed guignas from Chile.
Fig. 4 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. 4. Richness of gastrointestinal parasites in guignas from Chile, compared (a) by geographic zone and (b) by sex. p values show the statistical significance in the Mann-Whitney U test between (a) center-south and (b) females-males.
Fig. 2 in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark
Fig. 2. Overall parasite prevalence by age. Numbers on the x-axis indicate age in years. Numbers on top of the columns indicate number of individuals, in red for hedgehogs with endoparasites, in blue for hedgehogs without endoparasites. Statistically significant differences in proportions of hedgehogs with endoparasites versus without hedgehogs, were found between juveniles (<1 year) and age classes 1–6 years, and between hedgehogs of one year versus two years of age as shown in the upper right corner of the figure. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark
Fig. 4. Overall parasite prevalence by region. Numbers indicate number of individuals, in red for hedgehogs with parasites, in blue without. JNL denotes Jutland north of the Limfjord, and JSL abbreviates Jutland south of the Limfjord. Statistically significant differences in proportions of hedgehogs with endoparasites versus hedgehogs without endoparasites were found between Zealand and Jutland south of the Limfjord (JSL), and Zealand and Falster (p <0.05 in both cases). We removed seven individuals from the analyses (Jutland north of the Limfjord (n = 1), Jutland south of the Limfjord (n = 4), Lolland (n = 1), Bornholm (n = 1)), as they were the only individuals found in April and December, and four were only categorised as collected in "Summer 2016". (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 An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark
Fig. 1. A map representing Denmark and the geographical locations of the 299 dead European hedgehogs examined. Colours indicate the different species of endoparasites detected in each individual. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 10. Mimosphinctes rudicostatus Bogoslovsky, 1980, PIMUZ 28595, bed 48 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 10. Mimosphinctes rudicostatus Bogoslovsky, 1980, PIMUZ 28595, bed 48, Polygnathus inversus Zone, Dzhaus−beds, early Emsian, Khodzha− Kurgan Gorge, Zerashan Range, Uzbekistan. This individual had suffered from a deep fracture, which had caused an irritation of the mantle. This had the formation of a spiral trace as a consequence.
Fig. 13 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 13. Relation between phragmocone size and spiral pit diameter (A) and between whorl height and spiral pit diameter (B).
Fig. 7. Longitudinal section through the well preserved specimen PIMUZ 28583 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 7. Longitudinal section through the well preserved specimen PIMUZ 28583 of Sellanarcestes spp., Sellanarcestes wenkenbachi Zone, Emsian, Oufrane (S of Tata), Morocco. A. +/− median section displaying many "Housean pits", most with internal tube; overview. "Housean pits" are marked by white arrows. B. Three closely spaced pits, two displaying the internal tubes, the remaining void inside the pit is filled with a fine−grained sparitic matrix, note the continuous ammonoid shell layer covering the pits and the septum, which grew on the pit wall, note the distinguishable shell layers, which are recrystallised to varying degrees. C. A corroded pit with tube, note the continuation of the innermost ammonoid shell layer. D. Two adjacent fused pits, only the right pit shows the delicate internal tube, mural part of septum on the left.
Fig. 5 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 5. "Housean pits" type 3. Sobolewia nuciformis (Whidborne, 1889), three specimens kept under the same number (MNHN−R.08459), Givetian, Redjel Iamrad, Algeria, Jacques Follot collection. A. A heavily weathered specimen in which the erosion was most intense around the pits; lateral (A1) and (A2) dorsal views, weathered specimen, where the shell broke at the pits and weathering intensified in those radii. B. Lateral view of a specimen showing only two pits, additional pits probably covered by shell. C. The best preserved specimen, previously published in Korn and Klug (2002: fig. 52B), in ventral (C1) and lateral (C2) views, well preserved specimen, where the shell broke off only at the four lateral pits, showing the tube cross section in the pits (the globular structures in the centre of the pit at the bottom and on the left are artefactsfrom the production of the cast). Images taken from epoxy casts. All specimens coated with NH4Cl.
Fig. 6. A–C in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 6. A–C. "Housean pits" type 4, Ivoites sp. nov. B, early Emsian, middle Kaub Formation (Hunsrück Slate), W−Germany; the images were stretched in PhotoShop in order to reconstruct the original form. A. HS 371 (Bartels collection), Bundenbach (Eschenbach–Bocksberg quarry); note the flattened phragmocone. B. H 55a (Lehmann collection), Bundenbach (Eschenbach–Bocksberg quarry); note the spiral trace between the aperture and the first pit pair. C. SMF−HF 940 (Senckenberg collection), Herrenberg (Schielebach quarry). D, E. "Housean pits" type 5, early Emsian, Ouidane Chebbi, Tafilalt, Morocco, from Klug et al. (2008). D. Chebbites reisdorfi Klug, 2001, PIMUZ 7484; in lateral (D1) and ventral (showing pits) (D2) views. E. Gracilites maghribensis Klug, 2001, PIMUZ 7490; in ventral (showing pits) (E1) and lateral (E2) views. All specimens coated with NH4Cl except in A and C.
Fig. 9 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 9. Trematode (?) pits in the internal mould of an Early Devonian palaeotaxodont bivalve (modified after Klug et al. 2008b: pl. 3). Nuculoidea grandaeva (Goldfuss 1837), PIMUZ 7338, Faunule 2, Polygnathus gronbergi (Polygnathus excavatus) Zone, early Emsian, Ouidane Chebbi (Tafilalt, Morocco) in dorsal (A) and lateral (B) views.
Fig. 2 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 2. Palaeogeographic map for the Emsian showing occurrences of the genera Sellanarcestes and Anarcestes with and without "Housean pits" of type 1. Modified from Scotese (2001).
Fig. 3 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 3. "Housean pits" type 1. A. Sellanarcestes ebbighauseni Klug, 2002, GPIT 1871−171, Sellanarcestes wenkenbachi Zone, Emsian, northern Jebel Amessoui, Tafilalt, Morocco, from Klug (2002); in ventral (A1) and lateral (A2) views. B. Sellanarcestes cf. ebbighauseni Klug, 2002, PIMUZ 28582, Sellanarcestes wenkenbachi Zone, Emsian, Jebel Ouaoufilal, Tafilalt, Morocco; in lateral (B1) and ventral (B2) views. C. Large pits in Anarcestes sp., PIMUZ 28581, late Emsian, Jebel Mech Agrou, Tafilalt, Morocco; in lateral (C1) and ventral (C2) views. All specimens coated with NH4Cl.
Fig. 4 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 4. "Housean pits" type 2. A. Crispoceras tureki Klug, 2002, PIMUZ 28591, Pinacites jugleri Zone, Eifelian, Jebel Ouaoufilal, Tafilalt, Morocco; in dorsal (A1) and lateral (A2) views; A3, detail of A2, whose position is pointed out by the black arrow in A2, note the three pits (white arrows), the middle pit shows the pit filling and the base of the tube cross section. B. Crispoceras tureki Klug, 2002, PIMUZ 28590, Pinacites jugleri Zone, Eifelian, Jebel Ouaoufilal, Tafilalt, Morocco; in lateral (B1) and (B2) dorsal views, pits continue into the body chamber. C–E. Afromaenioceras sulcatostriatum Bensaïd, 1974, Givetian, Jebel Ouaoufilal, Tafilalt, Morocco; in ventral (C1, D1, E1) and lateral (C2, D2, E2) views. C. PIMUZ 28592. D. PIMUZ 28593. E. PIMUZ 28594. All specimens coated with NH4Cl except in A3.
Fig. 14 in Devonian pearls and ammonoid-endoparasite co-evolution
Fig. 14. Relation between the estimated amount of pits per half whorl and the ratio between pit size and phragmocone diameter.
Fig. 2 in Endoparasite loads and the efficacy of conventional anthelmintics against gastrointestinal nematodes in captive European bison
Fig. 2. Mean (±SE) number of Eimeria species in European bison without ungulate neighbors (N0) and kept near other ungulates (YES) for seasons, calculated in a generalized linear model. Differences were statistically significant in the pairwise comparison for autumn and winter (p values shown above the bars).
Fig. 1 in Endoparasite loads and the efficacy of conventional anthelmintics against gastrointestinal nematodes in captive European bison
Fig. 1. Location of coproscopically examined European bison enclosures and other ungulate species in the vicinity of these enclosures in Poland.
Fig. 2 in Parasites of pufferfish, Lagocephalus spp. and Torquigener flavimaculosus of the Israeli Mediterranean: A new case of Lessepsian endoparasites
Fig. 2. Multidimensional scaling (MDS) plot displaying the similarity of the parasite fauna of the four pufferfish species. Only infected pufferfish shown and one extreme outlier of Torquigener flavimaculosus excluded for a more compact display.
Fig. 1 in Parasites of pufferfish, Lagocephalus spp. and Torquigener flavimaculosus of the Israeli Mediterranean: A new case of Lessepsian endoparasites
Fig. 1. Habitus of alive (A) and mounted line-drawn (B) specimens of Maculifer dayawensis from the intestinal tract of Lagocephalus guentheri, including all visible characteristics. The black spots in the alive specimen – the pigment granules. Diagnostic characteristics of the parasite - the muscular post-oral ring (1), genital pore (2), cirrus sack (3), ovary dorsally behind left testes (4) and opposite testes (5), as well as vitelline follicles reaching up to the pharynx. Follicles extend over the whole body and are partially omitted in the drawing for the sake of clarity.
Fig. 1 in Applying a modified streamlined disease risk analysis framework to a platypus conservation translocation, with special consideration for the conservation of ecto- and endoparasites
Fig. 1. An outline of how parasite conservation can be considered in translocation planning, reproduced from Carlson et al. (2020).
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