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81 results for “Capreolus”
Fig. 3 in Detection and molecular characterization of the mosquito-borne filarial nematode Setaria tundra in Danish roe deer (Capreolus capreolus)
Fig. 3. Neighbor-Joining phylogenetic relationship of four isolates of Setaria tundra from distant localities in Denmark. The analysis was based on cox1 gene sequences (578 bp). Percentage bootstrap support from 1000 replicate samples is indicated at the right of the supported node. Accession numbers for sequences obtained from GenBank are given in parentheses, followed by origin of isolate, only applicable to S. tundra. The scale bar indicates distance.
Fig. 1 in Detection and molecular characterization of the mosquito-borne filarial nematode Setaria tundra in Danish roe deer (Capreolus capreolus)
Fig. 1. Geographical origin (black dots) of Setaria tundra recovered from six infected roe deer. A: October 2010, B: May 2011, C: December 2012, D: May 2013 (two cases), and E: March 2014.
Fig. 2 in Detection and molecular characterization of the mosquito-borne filarial nematode Setaria tundra in Danish roe deer (Capreolus capreolus)
Fig. 2. Morphology of adult worms of Setaria tundra (A‾C) and microfilaria (D and E) recovered from roe deer in Denmark. A: Cephalic region showing the bifid projections (bp) carried on top of a peribuccal crown (pc) and one of the four cephalic papillae (cp). B: Posterior end of male worm with papillae weakly visible (arrowheads). C: Posterior end of female worm showing a knob at the tip of the tail (arrow head), that possesses longitudinal grooves and pores, a papilla (pa), and a collar composed of a row of bosses (co). D: Microfilaria collected from a female worm. The length of the microfilaria including the sheath (white arrow heads) was approximately 316 Mm, whereas the microfilaria was approximately 287 Mm, with a blunt anterior end and a tapering posterior end. E: Setaria tundra coiled under the liver capsule (case 3). Scale bars indicated for all but figure E.
Fig. 1 in Habitat selection of the roe deer Capreolus capreolus (Artiodactyla: Cervidae) in an agroforestry system
Fig. 1 - Study area: Vallevecchia (Venice). The walked transects (T1 to T6) are highlighted in red. / Area di studio: Vallevecchia (Venezia). I transetti percorsi (da T1 a T6) sono evidenziati in rosso.
Fig. 4 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)
Fig. 4 Light and scanning electron microscopy images of male specimens of Linguatula sp. collected from Capreolus capreolus. A SEM of posterior hook (SPL1165-2), with sensory papillae #3. B Anterior hook with fulcrum (SPL1165-2). Scale bar = 100 µm. C Posterior hook with fulcrum (SPL1165-2). Scale bar = 100 µm. D Posterior hook opening "pit" (SPL1165-2), showing fine spines on cuticle (arrow). Scale bar = 10 µm. E Anterior hook base with fine spines (arrow) (SPL1165-2). Scale bar = 25 µm. F Buccal capsule (SPL1156-1). Scale bar = 100 µm. G SEM of male genital aperture with sensory papillae #4 on lateral edges (SPL1165-3). H SEM of tip of copulatory spicule emerging from male genital aperture (SPL1165- 2). I Dissected copulatory spicule (SPL1165-1). Scale bar = 100 µm
Fig. 1 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)
Fig. 1 Map of the collection locations for the pentastomes examined in this study. Locations are indicated by red (collected from Canis lupus), yellow (collected from Canis aureus), and blue (collected from Capreolus capreolus) markers. The number within the marker refers to the specimen listed in Table 1
Fig. 3 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)
Fig. 3 Scanning electron microscopy images of male specimens of Linguatula sp. collected from Capreolus capreolus. A Anterior end, ventral view (SPL1165-3), white box marks location of sensory sensillae presented in E; ga, genital atrium. B Lateral edge of body (SPL1165-2), ventral side to the right. C Posterior end of body, dorsal view (SPL1165-2), note absence of chloride cells in midline of dorsal side. D Abdominal annulus, ventral view (SPL1165-2), note single row of chloride cells and markings on posterior edge of annuli. E Sensory pore, ventral surface of anterior end (SPL1165-3)
Fig. 2 in Characterization of tongue worms, Linguatula spp. (Pentastomida) in Romania, with the first record of an unknown adult Linguatula from roe deer (Capreolus capreolus Linnaeus)
Fig. 2 Scanning electron microscopy images of a male specimen of Linguatula serrata (Frölich 1789) collected from Canis lupus (specimen number L4). A Anterior end of specimen, ventral view; ga, genital atrium. B Posterior hook with hook "pit" showing spines on wall (white box). C Spines on wall of hook "pit"
Fig. 1 in Prevalence and co-infection with tick-borne Anaplasma phagocytophilum and Babesia spp. in red deer (Cervus elaphus) and roe deer (Capreolus capreolus) in Southern Norway
Fig. 1. Phylogenetic tree of Babesia isolates and samples of this study (●), based on fragments of 18S rRNA, generated using the Maximum-Likelihood clustering method in MEGA 6 software (1000 replicates; bootstrap values indicated at the nodes). Abbreviations: AU - Austria, BE - Belgium, CA - Canada, DE - Germany, FR - France, HU - Hungary, IT - Italy, JP - Japan, LT - Lithuania, NO - Norway, PL - Poland, RU - Russia, SK - Slovakia, SP - Spain, TU - Turkey, US - United States.
Fig. 1 in Short Communication Alpine chamois Rupicapra rupicapra (L. 1758) and European roe deer Capreolus capreolus (L. 1758) close together at a salt lick
Fig. 1 - The positions of the three chamois (C), two roe deer (R), and two observers (O) at the first full sighting of the animals, when the shortest distance between chamois and roe deer was four metres, 27 metres the longest. / Le posizioni dei tre camosci (C), dei due caprioli (R) e dei due osservatori (O) nel momento del primo avvistamento completo degli animali, quando tra camosci e caprioli la minima distanza era 4 metri, la massima 27 metri.
Fig. 2 in Short Communication Alpine chamois Rupicapra rupicapra (L. 1758) and European roe deer Capreolus capreolus (L. 1758) close together at a salt lick
Fig. 2 - The roe deer and two chamois at the shortest interspecific distance (see Fig. 1) and the trampled and ravaged ground around their rock, suggesting the salt lick. / Il capriolo e i due camosci alla minima distanza interspecifica (vedi Fig. 1) e il terreno calpestato e rivoltato intorno alla loro roccia, indicativo di una salina.
Fig. 4 in First record of chronic Fascioloides magna infection in roe deer (Capreolus capreolus)
Fig. 4. Same liver as in Fig. 3. Left part of the liver contains new migratory channels. Note less pronounced hemorrhages and clean migratory channels, as well as traces of iron-porphyrin on surface of the livers.
Fig. 3 in First record of chronic Fascioloides magna infection in roe deer (Capreolus capreolus)
Fig. 3. Cut surface of roe deer liver. Note the pseudocyst and numerous ironporphyrin traces in the liver parenchyma and fluke extracted from the pseudocyst.
Fig. 1 in First record of chronic Fascioloides magna infection in roe deer (Capreolus capreolus)
Fig. 1. Acutely infected roe deer liver. Irregular liver surface with opaque Glissons capsule, traces of dark pigment and nodular protrusions (hemorrhages).
Fig. 5. H&E in First record of chronic Fascioloides magna infection in roe deer (Capreolus capreolus)
Fig. 5. H&E liver pseudocyst fragment (Sony alpha 6000). The center of the cyst containing numerous F. magna eggs, traces of free (P) and phagocytosed intracellular iron-porphyrin (IP) embedded in thick collagenous tissue (C), surrounded by numerous irregular bile ducts (B), new blood vessels (BV) and hypertrophied smooth muscle bundles. Magnification 2x.
Fig. 3 in A novel intermediate host for Taenia serialis (Gervais, 1847): The European roe deer (Capreolus capreolus L. 1758) from the Monti Sibillini National Park (MSNP), Italy
Fig. 3. Phylogenetic relationships between two species of Taenia (T. serialis and T. multiceps) and the sample obtained for this study (sample from roe deer).
Fig. 1. Microscope view 100 in A novel intermediate host for Taenia serialis (Gervais, 1847): The European roe deer (Capreolus capreolus L. 1758) from the Monti Sibillini National Park (MSNP), Italy
Fig. 1. Microscope view 100 magnifications of the scolex collected from one of the cysts recovered in a wild European roe deer.
Fig. 2 in A novel intermediate host for Taenia serialis (Gervais, 1847): The European roe deer (Capreolus capreolus L. 1758) from the Monti Sibillini National Park (MSNP), Italy
Fig. 2. Note the meningeal vessels' congestion and the suppurative exudate covering the meningeal surface.
Data from: Pan-European phylogeography of the European roe deer (Capreolus capreolus)
<p>To provide the most comprehensive picture of species phylogeny and phylogeography of European roe deer (<em>Capreolus</em> <em>capreolus</em>), we analysed mtDNA control region (610 bp) of 1469 samples of roe deer from Central and Eastern Europe and included in the analyses an additional 1,541 mtDNA sequences from GenBank from other regions of the continent. We detected two mtDNA lineages of the species: European and Siberian (an introgression of <em>C</em>. <em>pygargus</em> mtDNA into <em>C</em>. <em>capreolus</em>). The Siberian lineage was most frequent in the eastern part of the continent and declined towards Central Europe. The European lineage contained three clades (Central, Eastern and Western) composed of several subclades, many of which were separated in space. The Western clade appeared to have a discontinuous range from Portugal to Russia. Most of the subclades in the Central and the Eastern clades were under expansion during the Weichselian glacial period before the Last Glacial Maximum (LGM), while the expansion time of the Western clade overlapped with the Eemian interglacial. The high genetic diversity of extant roe deer is the result of their survival during the LGM probably in a large, contiguous range spanning from the Iberian Peninsula to the Caucasus Mts. and in two northern refugia.</p>
Data from: Pan-European phylogeography of the European roe deer (Capreolus capreolus)
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