Academic literature on the topic 'Triadobatrachus'

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Journal articles on the topic "Triadobatrachus"

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Ascarrunz, Eduardo, Jean-Claude Rage, Pierre Legreneur та Michel Laurin. "Triadobatrachus massinoti, the earliest known lissamphibian (Vertebrata: Tetrapoda) re-examined by μCT scan, and the evolution of trunk length in batrachians". Contributions to Zoology 85, № 2 (2016): 201–34. http://dx.doi.org/10.1163/18759866-08502004.

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Triadobatrachus massinotiis a batrachian known from a single fossil from the Early Triassic of Madagascar that presents a combination of apomorphic salientian and plesiomorphic batrachian characters. Herein we offer a revised description of the specimen based on X-ray micro-tomography data. We report previously unknown caudal vertebrae, possible mentomeckelians, and hidden parts of other structures. We also confirm the presence of a ventrolateral ledge on the opisthotic, and we rectify some previous interpretations. There are no cervical ribs and the jaw may have had an angular. The presacral
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Rage, Jean-Claude. "Triadobatrachus (Salientia, Amphibia), hier et aujourd'hui." Annales de Paléontologie 92, no. 2 (2006): 165–74. http://dx.doi.org/10.1016/j.annpal.2006.03.008.

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Jésus, Valerian J. P., Octávio Mateus, Jesper Milàn, and Lars B. Clemmensen. "First occurrence of a frog-like batrachian (Amphibia) in the Late Triassic Fleming Fjord Group, central East Greenland." Bulletin of the Geological Society of Denmark 70 (August 24, 2022): 117–30. http://dx.doi.org/10.37570/bgsd-2022-70-08.

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During the Triassic, Batrachia diverged into ancestors of frogs (Salientia) and salamanders (Caudata). Fossils of Triassic batrachians are rare and found only in a few outcrops, such as the Middle Sakamena Formation of Madagascar (Induan). Only three Triassic taxa have been described, the two early frogs Triadobatrachus and Czatkiobatrachus and the early salamander Triassurus. Here we describe a right ilium, collected in 1991, attributed to the first batrachian from the Late Triassic Carlsberg Fjord Member (Ørsted Dal Formation, Fleming Fjord Group) in the Jameson Land Basin, located in centra
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Rocek, Zbynek. "Origin and evolution of the frontoparietal complex in anurans." Amphibia-Reptilia 9, no. 4 (1988): 385–403. http://dx.doi.org/10.1163/156853888x00062.

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AbstractThe frontoparietal is a unique feature of anurans, not only if this group is compared with other amphibians, but also with other vertebrates as well. It is often used as an important character in anuran systematics. However, little is still known about its evolutionary origin and significance. This is the reason why its state in Triadobatrachus and fossil anurans was examined, and compared with the condition in osteolepiforms and labyrinthodonts. Besides that also an information from the larval development was taken into consideration. It follows from all these data that the frontopari
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Sigurdsen, Trond, David M. Green, and Phillip J. Bishop. "Did Triadobatrachus Jump? Morphology and Evolution of the Anuran Forelimb in Relation to Locomotion in Early Salientians." Fieldiana Life and Earth Sciences 5 (October 18, 2012): 77–89. http://dx.doi.org/10.3158/2158-5520-5.1.77.

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Schoch, Rainer R. "The putative lissamphibian stem-group: phylogeny and evolution of the dissorophoid temnospondyls." Journal of Paleontology 93, no. 1 (2018): 137–56. http://dx.doi.org/10.1017/jpa.2018.67.

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AbstractDissorophoid temnospondyls are widely considered to have given rise to some or all modern amphibians (Lissamphibia), but their ingroup relationships still bear major unresolved questions. An inclusive phylogenetic analysis of dissorophoids gives new insights into the large-scale topology of relationships. Based on a TNT 1.5 analysis (33 taxa, 108 characters), the enigmatic taxonPerryellais found to nest just outside Dissorophoidea (phylogenetic defintion), but shares a range of synapomorphies with this clade. The dissorophoids proper are found to encompass a first dichotomy between the
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Maren, JANSEN, and MARJANOVIĆ David. "The scratch-digging lifestyle of the Permian "microsaur" Batropetes Carroll & Gaskill, 1971 as a model for the exaptative origin of jumping locomotion in frogs." Comptes Rendus Palevol 21, no. 23 (2022): 463–88. https://doi.org/10.5852/cr-palevol2022v21a23.

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Recent studies have shown that the Triassic stem-frog <em>Triadobatrachus </em>Kuhn, 1962 lacked the ability to jump, but nonetheless had the forelimb strength to withstand the impact of landing from a jump. We propose a hypothesis to resolve this pseudoparadox: the strengthened forelimbs are former adaptations to forelimb-based digging that later made jumping possible by exaptation. Micro-CT data from a skeleton of <em>Batropetes palatinus </em>Glienke, 2015 reveal thin cortical bone, confirming <em>Batropetes </em>Carroll&nbsp;&amp; Gaskill, 1971 as terrestrial. Combining adaptations to walk
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Stocker, Michelle R., Sterling J. Nesbitt, Ben T. Kligman, et al. "The earliest equatorial record of frogs from the Late Triassic of Arizona." Biology Letters 15, no. 2 (2019): 20180922. http://dx.doi.org/10.1098/rsbl.2018.0922.

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Crown-group frogs (Anura) originated over 200 Ma according to molecular phylogenetic analyses, though only a few fossils from high latitudes chronicle the first approximately 60 Myr of frog evolution and distribution. We report fossils that represent both the first Late Triassic and the earliest equatorial record of Salientia, the group that includes stem and crown-frogs. These small fossils consist of complete and partial ilia with anteriorly directed, elongate and distally hollow iliac blades. These features of these ilia, including the lack of a prominent dorsal protuberance and a shaft tha
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Lires, Andrés I., Ignacio M. Soto, and Raúl O. Gómez. "Walk before you jump: new insights on early frog locomotion from the oldest known salientian." Paleobiology 42, no. 4 (2016): 612–23. http://dx.doi.org/10.1017/pab.2016.11.

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AbstractUnderstanding the evolution of a Bauplan starts with discriminating phylogenetic signal from adaptation and the latter from exaptation in the observed biodiversity. Whether traits have predated, accompanied, or followed evolution of particular functions is the basic inference to establish the type of explanations required to determine morphological evolution. To accomplish this, we focus in a particular group of vertebrates, the anurans. Frogs and toads have a unique Bauplan among vertebrates, with a set of postcranial features that have been considered adaptations to jumping locomotio
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10

Maren JANSEN, undefined, and David MARJANOVIĆ. "The scratch-digging lifestyle of the Permian “microsaur” Batropetes Carroll & Gaskill, 1971 as a model for the exaptative origin of jumping locomotion in frogs." Comptes Rendus Palevol, no. 23 (July 6, 2022). http://dx.doi.org/10.5852/cr-palevol2022v21a23.

Full text
Abstract:
Recent studies have shown that the Triassic stem-frog Triadobatrachus Kuhn, 1962 lacked the ability to jump, but nonetheless had the forelimb strength to withstand the impact of landing from a jump. We propose a hypothesis to resolve this pseudoparadox: the strengthened forelimbs are former adaptations to forelimb-based digging that later made jumping possible by exaptation. Micro-CT data from a skeleton of Batropetes palatinus Glienke, 2015 reveal thin cortical bone, confirming Batropetes Carroll &amp; Gaskill, 1971 as terrestrial. Combining adaptations to walking and digging, confirmed by st
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