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256 results for “Salamandridae”
FIGURE 6 in Salamandridae) using molecular and morphological data. Revalidation of the taxon Pleurodeles nebulosus (Guichenot, 1850)
FIGURE 6. Ventral aspect of the skull of A. adult P. p o i re t i, BMNH 1920.1. 20.1383 (Bône) and B. adult P. nebulosus, BMNH 130 a (Algiers).
FIGURE 1 in Salamandridae) using molecular and morphological data. Revalidation of the taxon Pleurodeles nebulosus (Guichenot, 1850)
FIGURE 1. Map of North Africa showing localities of Pleurodeles used in the present study. See Table 1 and Fig. 5 for further details. The dashed line delimits the approximate distribution range of P. poireti. We refer to it in the text as the Edough Peninsula.
FIGURE 3 in Salamandridae) using molecular and morphological data. Revalidation of the taxon Pleurodeles nebulosus (Guichenot, 1850)
FIGURE 3. Photograph showing nine specimens of P. p i o i re t i (above) and four P. nebulosus (below). A 23 centimetres scale bar is shown on the lefthand side of the picture; black rectangles and intermediate white spaces all represent 1 cm. Numbers above the specimens refer to: 1. BMNH 1920.1. 20.1327. 2, largest specimen of P. p oireti included in the present study. Female from Bône (Annaba); 2. BMNH 1946.9. 6.77, male of P. poireti from Mount Edough; 3. BMNH 1946.9. 6.78, male of P. p o i re t i from Mount Edough; 4. BMNH 1946.9. 6.79, male of P. poireti from Mount Edough; 5. BMNH 1946.9. 6.80, male of P. p o i re t i from Mount Edough; 6. BMNH 1946.9. 6.81, male of P. p o i re t i from Mount Edough; 7. BMNH 1946.9. 6.79, male of P. poireti from Mount Edough; 8. MNHNP 4744, female, paralectotype of P. p o i re t i from Bône (Annaba); 9. MNHNP 4744 A, male, lectotype of P. p o i ret i from Bône (Annaba); 10. BMNH 1.1.3.1. a, largest specimen of P nebulosus recorded to date. Male from N. Africa; 11. BMNH 88.4. 9.3, female of P. nebulosus from Algiers; 12. BMNH 88.4. 4, male of P. nebulosus from Algiers; 13. MNHNP 1442, female, lectotype of P. nebulosus from Algiers.
Fig. 2 in Assessing The Abundance Of Caucasian Salamander, Mertensiella Caucasica (Caudata, Salamandridae), With N-Mixture Model In Northeastern Anatolia
Fig. 2. The average abundance of Caucasian salamanders from the East Black Sea Region, Turkey. X-axis shows the sampling plots number in each city; Y-axis shows the estimated population size.
Fig. 2 in Ventral And Lateral Spot Patterns Differentiation Between Three Smooth Newt Species (Amphibia: Salamandridae: Lissotriton)
Fig. 2. Color patterns of smooth newt species. Lissotriton schmidtleri: males from Domurcalı (lateral view) and Dursunköy (ventral view), females from Yassıören (lateral view) and Ka- racabey (ventral view), Turkey; L. vulgaris: Gatchina, Russia; L. kosswigi: males from Mollafeneri (lateral view) and Hacılar (ventral view), females from Alibahadır Köyü, Turkey; L. lanzi: males from Ldzaa (lateral view) and Sukhum (ventral view), females from Ldzaa
Fig. 1 in Ventral And Lateral Spot Patterns Differentiation Between Three Smooth Newt Species (Amphibia: Salamandridae: Lissotriton)
Fig. 1. Distribution of Lissotriton vulgaris, L. schmidtleri and L. kosswigi in the Western Palearctic (A) and western Turkey (B). Numbers for localities are given in Table 1
Fig. 4 in Ventral And Lateral Spot Patterns Differentiation Between Three Smooth Newt Species (Amphibia: Salamandridae: Lissotriton)
Fig. 4. Plot of centroids for females (A) and males (B) of Lissotriton kosswigi, L. schmidtleri and L. vulgaris in the space of the first and second canonical discriminant axes
Fig. 3 in Ventral And Lateral Spot Patterns Differentiation Between Three Smooth Newt Species (Amphibia: Salamandridae: Lissotriton)
Fig. 3. Polygons selected on the ventral surface of newts (A) and types of dark spot arrangements located on the border between lateral and ventral surfaces (B), where r is random
Figure 5 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China
Figure 5. Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov. in preserved status. A–B. Male holotype, GZNU20180806001, dorsal and ventral views. C–D. Female paratype, GZNU20180607001, dorsal and ventral views. E. Female paratype, GZNU20180607001, dorsal view of head. F. Female paratype, GZNU20180607001, view of oral cavity (yellow arrows represent vomerine teeth). Scale bars: A–D = 5.0 mm; E–F = 4.0 mm.
Figure 6 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China
Figure 6. Habitat and eggs of Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov. at the type locality. A. Microhabitats. B. Individual found in the type locality. C. Eggs laid by GZNU20180607001 on 7 June 2018. D. Individual GZNU20180608001 collected on 8 June 2018 in Kuankuoshui National Nature Reserve.
Figure 4 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China
Figure 4. Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov. in life. A–C. Male holotype, GZNU20180806001, dorsal, ventral, and dorsolateral views. D–F. Female paratype, GZNU20180607001, dorsal, ventral, and dorsolateral views. H–I. Male holotype, GZNU20180806001, ventral view of the hand, foot, and cloaca. J–L. Female paratype, GZNU20180607001, ventral view of the hand, foot, and cloaca (yellow arrow). All photos were taken at around 9:00 am.
Figure 2 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China
Figure 2. Bayesian inference (BI) tree based on 16S+ND2 gene sequences. Bayesian posterior probabilities (BPP) from BI analyses/ ultrafast bootstrap supports (UFB) from ML analyses were noted beside nodes. The scale bar represents 0.04 nucleotide substitutions per site. The numbers at the tip of branches correspond to the ID numbers in Table 1.
Figure 1 in A new species of the genus Tylototriton (Amphibia: Urodela: Salamandridae) from the Eastern Dalou Mountains in Guizhou, China
Figure 1. Sampling localities of the Tylototriton daloushanensis Zhou, Xiao & Luo, sp. nov., T. maolanensis, and T. kweichowensis in Guizhou, China. A. Huoqiuba Nature Reserve, Suiyang County. B. Kuankuoshui National Nature Reserve, Suiyang County. C. Maolan National Nature Reserve, Libo County. D. Nayong County.
Fig. 3 in Distribution range expansion of Salamandra infraimmaculata Martens, 1885 (Caudata: Salamandridae) in Anatolia, Turkey, with a new locality record
Fig. 3. Predicted distribution of Salamandra infraimmaculata under current climatic conditions. Warm colors (red and yellow) show suitable habitats, whereas the blue color represents unsuitable habitats for S. infraimmaculata.
Fig. 2 in Distribution range expansion of Salamandra infraimmaculata Martens, 1885 (Caudata: Salamandridae) in Anatolia, Turkey, with a new locality record
Fig. 2. Distribution patterns of Salamandra infraimmaculata throughout southern Anatolia together with the new locality record.
Fig. 1 in Distribution range expansion of Salamandra infraimmaculata Martens, 1885 (Caudata: Salamandridae) in Anatolia, Turkey, with a new locality record
Fig. 1. Samples of Salamandra infraimmaculata captured from the new locality: (A) male and (B) female.
Fig. 4 in Distribution range expansion of Salamandra infraimmaculata Martens, 1885 (Caudata: Salamandridae) in Anatolia, Turkey, with a new locality record
Fig. 4. The marginal response curves of S. infraimmaculata to (A) Minimum Temperature of Coldest Month (Bio6), (B) Mean Temperature of Wettest Quarter (Bio8), and (C) Precipitation of Warmest Quarter (Bio18). The red lines and blue shading respectively show the mean responses of the 30 replicate MaxEnt runs and the mean plus/minus one standard deviation.
Fig. 6 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives
Fig. 6. Tylototriton ziegleri larvae from Bao Lac district, Cao Bang Province with indication of the corresponding developmental stage and scale. Photographs of stages 27 to 36 are from preserved eggs photographed under a digital microscope (photos C. Michel) and photographs of stages 44 and 45 are from individuals in life kept at the Me Linh station (photos T. Ziegler).
Fig. 4 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives
Fig. 4. Drawing of a formol-preserved larva of Tylototriton ziegleri at stage 35. Drawing C. Michel.
Fig. 2 in Larval development and breeding ecology of Ziegler's Crocodile Newt, Tylototriton ziegleri Nishikawa, Matsui and Nguyen, 2013 (Caudata: Salamandridae), compared to other Tylototriton representatives
Fig. 2. Percentage of the number of adults of Tylototriton vietnamensis and T. ziegleri found at each interval of percentage of canopy cover measured above the water of the breeding site.
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International Brain Laboratory public data
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OpenNeuro
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