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36 results for “Anas platyrhynchos”
Fig. 4 in Morphometric Analysis Of Сapillaria Anatis (Nematoda, Capillariidae) From Anas Platyrhynchos Domesticus
Fig. 4. ♀ Сapillaria anatis: a — general view; b — body at vulva; с — eggs in uterus; d — tail end; Va — vulva, Vg — vagina, U — uterus, E — eggs, Es — posterior part of esophagus.
Fig. 2 in Morphometric Analysis Of Сapillaria Anatis (Nematoda, Capillariidae) From Anas Platyrhynchos Domesticus
Fig. 2. Morphometric parameters of sexual dimorphism in Сapillaria anatis: а — length of body (mm); b — length of trophic-sensory part (anterior body part) (mm); c — length of trophic-reproductive part (posterior body part) (mm); d — width of body at the middle of head end (μm); e — width of body at the esophago-intestinal junction (μm); f — width of body at the middle (μm); g — width of body at the middle of tail end (μm); *Р <0.05 compared to values of parameters in Ơ; х ± SD, Min–Мax; n = 15
Fig. 5 in Helminths Of The Mallard, Anas Platyrhynchos (Aves, Anatidae) In Ukraine: Analysis Of The Diversity In Mixed Forest Zone And The Black Sea Region
Fig. 5. Configuration of 2-dimensional MDS for specimens of Mallard from the mixed forest zone (P) and from the steppe zone (B) with overlapping clusters at similarity level of 15 %.
Fig. 3 in Helminths Of The Mallard, Anas Platyrhynchos (Aves, Anatidae) In Ukraine: Analysis Of The Diversity In Mixed Forest Zone And The Black Sea Region
Fig. 3. Prevalence (with lower and upper confidence intervals at significant level 95 %) and mean intensity (with range; in case when only one or two birds were infected by a certain type of helminth, then the actual intensity values are given) of Mallard´s infection with: A — trematodes from the mixed forest zone; B — trematodes from the steppe zone. * Logarithmic scale was used
Fig. 2 in Description of SarCoCYSTIS PlaTYrhYNChoSI n. sp. (Apicomplexa: Sarcocystidae) from domestic ducks ANaS PlaTYrhYNChoS (Anseriformes: Anatidae) in China
Fig. 2 Phylogenetic trees of selected members of Sarcocystis species. The trees were conducted using 18S rDNA (a), 28S rDNA (b) and mcox1 (c) sequences using maximum likelihood (ML) with the Kimura 2–parameter, Hasegawa–Kishino–Yano and Hasegawa–Kishino–Yano models, respectively. The values between the branches represent bootstrap values per 1000 replicates. Values <50% are not shown. Besnoitia besnoiti, Cystoisopora suis, Toxoplasam gondii or Hammondia heydorni were selected to root these trees.The newly obtained sequences of the 18S rDNA (OP480004), 28S rDNA (OP480005) and mtcox1 (OP485287) for Sarcocystis platyrhynchosi n. sp. are shown in bold. The phylogenetic trees inferred from the three genes had similar topologies, and Sarocystis platyrhynchosi formed a separate branch within a group encompassing Sarcocystis spp. obtained from avian or carnivorous intermediate hosts and avian marsupial, or carnivorous definitive hosts
Fig. 1 in Description of SarCoCYSTIS PlaTYrhYNChoSI n. sp. (Apicomplexa: Sarcocystidae) from domestic ducks ANaS PlaTYrhYNChoS (Anseriformes: Anatidae) in China
Fig. 1 Morphological characteristics of Sarcocystis platyrhynchosi n. sp. isolated from the skeletal muscle of domestic ducks. a Light microscopy (LM) micrograph of a sarcocyst (unstained). Note the short brush-like villar protrusions (vps). b LM micrograph of lancet-like bradyzoites (unstained). c Transmission electron microscopy (TEM) micrograph of a sarcocyst. Note the lanceolated villar protrusions (vps) and the bundles of microtubes (mt) within the vps. d TEM micrograph of a sarcocyst. Note the narrowed stalk (arrowhead) of the vps, bundled mt extending into the ground substance (gs) and the smooth electron dense layer (edl) lining the vps
Figure 3 in Ontogeny of Chenophila platyrhynchos sp. nov. (Acari: Syringophilidae), an ectoparasite of the Mallard Anas platyrhynchos (Anseriformes: Anatidae)
Figure 3. Chenophila platyrhynchos sp. nov., tritonymph: A) dorsal view, B) ventral view, C) gnathosoma in dorsal view, D) gnathosoma in ventral view, E) peritremes, F) solenidia of leg I.
Figure 4 in Ontogeny of Chenophila platyrhynchos sp. nov. (Acari: Syringophilidae), an ectoparasite of the Mallard Anas platyrhynchos (Anseriformes: Anatidae)
Figure 4. Chenophila platyrhynchos sp. nov., protonymph: A) dorsal view, B) ventral view, C) gnathosoma in dorsal view, D) gnathosoma in ventral view, E) peritremes, F) tarsus I in dorsal view, G) tarsus II in dorsal view.
Fig. 2. Sarcocyst and bradyzoite morphology. A. Isolated S in Sarcocystis rileyi (Apicomplexa) in Anas platyrhynchos in Europe with a potential for spread
Fig. 2. Sarcocyst and bradyzoite morphology. A. Isolated S. rileyi sarcocysts (mean length 5.25 mm) mounted in Aquatex, B. Wet smear of liberated bradyzoites (mean length 13.48 μm) from a sarcocyst of S. rileyi, C. Histological section of a sarcocyst in the musculature of the mallard (scale bar 100 μm), D. Histological section of a S. rileyi sarcocyst in pectoral musculature of male mallard showing densely packed bradyzoites with strongly stained nuclei. Haematoxylin staining. DePeX mounting, (scale bar 100 μm).
Fig. 3 in Sarcocystis rileyi (Apicomplexa) in Anas platyrhynchos in Europe with a potential for spread
Fig. 3. Alignment of PCR products. The shading on the scale at the top indicates a part of sequences, which resulted in no proper similarity towards any sequence at GenBank. Arrows indicate the features of the combined sequence (MZ151434). The grey bars indicate GenBank sequences with 100% similarity to the obtained sequences. The black bars indicate obtained PCR products, which notations at the left are "Forward primer vs Reverse primer".
Fig. 1 in Sarcocystis rileyi (Apicomplexa) in Anas platyrhynchos in Europe with a potential for spread
Fig. 1. Sarcocystis rileyi sarcocysts in mallard musculature. A. Pectoral musculature, B. Dorsal musculature, C. Hand and arm musculature, D. Leg musculature.
Fig. 1 in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 1. Proved occurrence of R. auricularia snails in Hungarian habitats based on museum collections and own investigations. The species was detected in artificial ponds or canals (yellow dots: living specimens; green dots: shells) and also in natural habitats (red dots: living specimens; blue dots: shells). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 8. a, b in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 8. a, b. Maximum likelihood tree of the samples of Trichobilharzia franki and Bilharziella polonica from the present study (a COI, b 28S) in relation to other schistostomatid sequences deposited in GenBank. Bootstrap values are given at the nodes; posterior probabilities for Bayesian inference are shown behind the bootstrap values. Unsupported nodes by BI are marked with a hyphen. Samples from the present study are in bold. The scale bar indicates the expected number of substitutions per sit.
Fig. 6. A in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 6. A hemalaun-stained Dendritobilharzia male from the liver of a mallard. Every scale under the specimen is equal to a millimetre.
Fig. 3. A in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 3. A complete specimen of native Trichobilharzia male in cell suspension from the liver of a mallard.
Fig. 2 in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 2. The shape of bursa copulatrix of the adult R. auricularia is spherical and the stalk is long (A), while the bursa copulatrix of Radix balthica is oval and stalk is short (B). This anatomical structure seems the most reliable morphological difference to distinguish of the two most common Radix species in Hungary, but can only be studied on sexually mature and non-trematode infected specimens (Juh´asz, 2018) The length of the dissected organs is about 1 cm.
Fig. 1 in Morphometric Analysis Of Сapillaria Anatis (Nematoda, Capillariidae) From Anas Platyrhynchos Domesticus
Fig. 1. Head end of Сapillaria anatis.
Ánade real (Anas platyrhynchos)
**Ejemplar:** *Anas platyrhynchos* **Nombre común**: Ánade real, ànec collverd **Descripción:** Cráneo largo, ancho, plano y redondeado. Macho 10 meses. Alimentación plantas acuáticas, y también pequeños invertebrados y peces. Presenta un marcado dimorfismo sexual. Altura (5 cm), anchura (7 cm) y profundidad (16 cm). **Sigla museo, colección y entidad:** VER0000441. Colección del Dpto. de Zoología (Facultad Ciencias Biológicas). MUVHN. **Técnica digitalización / modelo**: escaneado superficial, escáner 3D Einscan Pro **Software empleado**: einscan v3.1.0.2, modo manual con plataforma giratoria, calidad media **Autor digitalización:** Natalia Conejero-Ortega **Cita ejemplar:** modelo 3D Colección cráneos de aves del Dpto. de Zoología. Museo Universitat de València de Historia Natural (MUVHN).  VER0000075. Ejemplar taxidermizado. Colección Histórica de Aves MUVHN. 1932. Source: Objaverse 1.0 / Sketchfab
Fig. 5 in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 5. Male Bilharziella polonica from the liver of a mallard.
Fig. 8 in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 8. (continued).
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