Academic literature on the topic 'Hynobiid salamanders'

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Journal articles on the topic "Hynobiid salamanders"

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Syromyatnikova, Elena V. "New Neogene Hynobiidae (Amphibia: Caudata) from Eastern Europe." Russian Journal of Herpetology 29, no. 3 (2022): 156–60. http://dx.doi.org/10.30906/1026-2296-2022-29-3-156-160.

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Fossil records of the Asiatic salamanders (Hynobiidae) are extremely scarce. The fossil European hynobiids come from a few localities of the Miocene-Pleistocene age and potentially suggest that in the past they were widely distributed across the European continent. This paper describes new Neogene records of Hynobiidae from the Late Miocene of Gritsev (Ukraine) and the Late Pliocene of Zhukovsky Mayak (Russia) localities. The hynobiids from Gritsev and Zhukovsky Mayak are the first records of hynobiid salamanders from certain time intervals of the corresponding regions and partly fill the exis
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Xiong, Jianli, Xiuying Liu, Liyan Qing, and Xiaomao Zeng. "Comparison of vomerine tooth rows in juvenile and adult Hynobius guabangshanensis (Urodela: Hynobiidae)." Vertebrate Zoology 64 (July 15, 2014): 215–20. https://doi.org/10.3897/vz.64.e31482.

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In this note, the vomerine tooth rows of juveniles and adults H. guabangshanensis are described and compared. The vomerine tooth rows are long and posteriorly directed, and arranged in a V-shape in adults while short and slightly arched, parallel to the premaxilla and maxilla in juveniles. The vomerine tooth rows of juveniles are similar to the aquatic salamanders, which feed by suction in water, and the vomerine tooth rows function in hindering escape of prey. The vomerine tooth rows of adults are resemble with terrestrial salamanders, which use inertial feeding or protruding tongue to captur
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Iizuka, K., J. Kezer, and T. Seto. "Karyotypes of two rare species of hynobiid salamanders from Taiwan, Hynobius sonani (Maki) and Hynobius formosanus Maki (Urodela)." Genetica 78, no. 2 (1988): 105–10. http://dx.doi.org/10.1007/bf00058841.

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Tsuneki, K., M. Ouji, H. Akiyoshi, and K. Ichihara. "Absence of blood vessels in the brain parenchyma of hynobiid salamanders." Experientia 41, no. 11 (1985): 1400–1402. http://dx.doi.org/10.1007/bf01950004.

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Xiong, Jianli, Yanan Zhang, Yuanye Sun, et al. "Comparison of hematological parameters in two different high altitudinal populations of Batrachuperus pinchonii (Amphibian: Urodela)." Amphibia-Reptilia 39, no. 1 (2018): 11–20. http://dx.doi.org/10.1163/15685381-00003142.

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Hematological parameters are key to reflect the health status of animals and their physiological adaptation to the environment. However, few studies focused on the inter- and intra-specific variations of hematological parameters in hynobiid salamanders. Here, we examined the hematological parameters of the stream salamander,Batrachuperus pinchonii, originating from two different altitudinal populations to explore their intra-specific variation. Sexual dimorphism is only present in the erythrocyte count and males have higher mean values than females. The morphometric values of erythrocyte, hemo
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Sato, Hiroshi, Sadao Ihara, Osamu Inaba, and Yumi Une. "IDENTIFICATION OF EURYHELMIS COSTARICENSIS METACERCARIAE IN THE SKIN OF TOHOKU HYNOBIID SALAMANDERS (HYNOBIUS LICHENATUS), NORTHEASTERN HONSHU, JAPAN." Journal of Wildlife Diseases 46, no. 3 (2010): 832–42. http://dx.doi.org/10.7589/0090-3558-46.3.832.

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Jia, Jia, and Ke-Qin Gao. "A new hynobiid-like salamander (Amphibia, Urodela) from Inner Mongolia, China, provides a rare case study of developmental features in an Early Cretaceous fossil urodele." PeerJ 4 (October 5, 2016): e2499. http://dx.doi.org/10.7717/peerj.2499.

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A new fossil salamander,Nuominerpeton aquilonaris(gen. et sp. nov.), is named and described based on specimens from the Lower Cretaceous Guanghua Formation of Inner Mongolia, China. The new discovery documents a far northern occurrence of Early Cretaceous salamanders in China, extending the geographic distribution for the Mesozoic fossil record of the group from the Jehol area (40th–45th parallel north) to near the 49th parallel north. The new salamander is characterized by having the orbitosphenoid semicircular in shape; coracoid plate of the scapulocoracoid greatly expanded with a convex ven
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Hasegawa, Hideo, and Kanto Nishikawa. "New Species of Kathlaniid (Nematoda: Cosmocercoidea) Collected From Hynobiid Salamanders in Japan." Journal of Parasitology 95, no. 1 (2009): 186–90. http://dx.doi.org/10.1645/ge-1635.1.

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Stöck, Matthias, Fatemeh Fakharzadeh, Heiner Kuhl, et al. "Shedding Light on a Secretive Tertiary Urodelean Relict: Hynobiid Salamanders (Paradactylodon persicus s.l.) from Iran, Illuminated by Phylogeographic, Developmental, and Transcriptomic Data." Genes 10, no. 4 (2019): 306. http://dx.doi.org/10.3390/genes10040306.

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The Hyrcanian Forests present a unique Tertiary relict ecosystem, covering the northern Elburz and Talysh Ranges (Iran, Azerbaijan), a poorly investigated, unique biodiversity hotspot with many cryptic species. Since the 1970s, two nominal species of Urodela, Hynobiidae, Batrachuperus (later: Paradactylodon) have been described: Paradactylodon persicus from northwestern and P. gorganensis from northeastern Iran. Although P. gorganensis has been involved in studies on phylogeny and development, there is little data on the phylogeography, systematics, and development of the genus throughout the
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WEISROCK, DAVID W., J. ROBERT MACEY, MASAFUMI MATSUI, and DANIEL G. MULCAHY. "Molecular phylogenetic reconstruction of the endemic Asian salamander family Hynobiidae (Amphibia, Caudata)." Zootaxa 3626, no. 1 (2013): 77–93. http://dx.doi.org/10.11646/zootaxa.3626.1.3.

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The salamander family Hynobiidae contains over 50 species and has been the subject of a number of molecular phylo-genetic investigations aimed at reconstructing branches across the entire family. In general, studies using the greatest amount of sequence data have used reduced taxon sampling, while the study with the greatest taxon sampling has used a limited sequence data set. Here, we provide insights into the phylogenetic history of the Hynobiidae using both dense taxon sampling and a large mitochondrial DNA sequence data set. We report exclusive new mitochondrial DNA data of 2566 aligned ba
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Dissertations / Theses on the topic "Hynobiid salamanders"

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Komatsu, Yukihiro. "Cause and consequence of cannibalistic polyphenism in larval salamander Hynobius retardatus." 京都大学 (Kyoto University), 2001. http://hdl.handle.net/2433/150857.

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Lai, June-Shiang, and 賴俊祥. "Systematic of Taiwanese Hynobius Salamanders and the Studies of Ecology and Population Genetics of Hynobius arisanensis." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/g2j996.

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博士<br>國立臺灣師範大學<br>生命科學研究所<br>96<br>The species diversity of Taiwanese Hynobius salamanders has long been debated. In this study, I analyzed morphological and molecular data from these taxonomically problematic salamanders. My results showed that there are five distinct molecular clades of Taiwanese salamanders that match morphological differences and are indicative of specie`s-level recognition. Three species corroborate previous finding, while the other two are described as new species. The distribution survey of Alishan salamander (Hynobius arisanensis) in Alishan Areas was conducted in 36 f
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Book chapters on the topic "Hynobiid salamanders"

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Kohno, Sei-ichi, Masaki Kuro-o, and Chikako Ikebe. "Cytogenetics and Evolution of Hynobiid Salamanders." In Amphibian Cytogenetics and Evolution. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-12-297880-7.50008-1.

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Vieites, David R., Peng Zhang, and David B. Wake. "Salamanders (Caudata)." In The Timetree of Life. Oxford University PressOxford, 2009. http://dx.doi.org/10.1093/oso/9780199535033.003.0050.

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Abstract Salamanders form a monophyletic group, constituting one of the three orders of modern amphibians (Lissamphibia), together with frogs and caecilians. Salamanders comprise the second most species-rich order of amphibians (1) and are typically classified in 10 families, with ca. 68% of the species belonging to the Family Plethodontidae. thebody plan has remained relatively stable since the Jurassic (2, 3) (Fig. 1), displaying several features that in combination distinguish it from the body plan of other amphibians: presence of a tail both in larval and adult phases, two pairs of limbs of equal size (when present) set perpendicular to the body, presence of teeth on both jaws, presence of ribs on most trunk vertebrae, and absence of several skull bones (4). Here we review the phylogenetic relationships and the divergence times of salamander families. thefamilies are grouped into Ave suborders: Cryptobranchoidea (Cryptobranchidae and Hynobiidae), Sirenoidea (Sirenidae), Salamandroidea (Salamandridae, Ambystomatidae, Dicamptodontidae), Proteoidea (Proteidae), and Plethodontoidea (Plethodontidae, Rhyacotritonidae, and Amphiumidae). Despite the increasing number of studies and data addressing the phylogeny of salamander families, their relationships are di1cult to resolve. Several relationships are consistently recovered with diBerent data sets, while the positions of others, in particular the sirenids and proteids, have remained contentious.
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"Hynobiidae Cope, 1859." In Salamanders of the Old World. KNNV Publishing, 2014. http://dx.doi.org/10.1163/9789004285620_004.

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"Hynobiidae Cope, 1859." In Salamanders of the Old World. KNNV Publishing, 2014. http://dx.doi.org/10.1163/9789004285620_007.

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