scholarly journals Northward dispersal of dinosaurs from Gondwana to Greenland at the mid-Norian (215–212 Ma, Late Triassic) dip in atmospheric pCO2

2021 ◽  
Vol 118 (8) ◽  
pp. e2020778118
Author(s):  
Dennis V. Kent ◽  
Lars B. Clemmensen

The earliest dinosaurs (theropods and sauropodomorphs) are found in fossiliferous early Late Triassic strata dated to about 230 million years ago (Ma), mainly in northwestern Argentina and southern Brazil in the Southern Hemisphere temperate belt of what was Gondwana in Pangea. Sauropodomorphs, which are not known for the entire Triassic in then tropical North America, eventually appear 15 million years later in the Northern Hemisphere temperate belt of Laurasia. The Pangea supercontinent was traversable in principle by terrestrial vertebrates, so the main barrier to be surmounted for dispersal between hemispheres was likely to be climatic; in particular, the intense aridity of tropical desert belts and unstable climate in the equatorial humid belt accompanying high atmospheric pCO2 that characterized the Late Triassic. We revisited the chronostratigraphy of the dinosaur-bearing Fleming Fjord Group of central East Greenland and, with additional data, produced a correlation of a detailed magnetostratigraphy from more than 325 m of composite section from two field areas to the age-calibrated astrochronostratigraphic polarity time scale. This age model places the earliest occurrence of sauropodomorphs (Plateosaurus) in their northernmost range to ∼214 Ma. The timing is within the 215 to 212 Ma (mid-Norian) window of a major, robust dip in atmospheric pCO2 of uncertain origin but which may have resulted in sufficiently lowered climate barriers that facilitated the initial major dispersal of the herbivorous sauropodomorphs to the temperate belt of the Northern Hemisphere. Indications are that carnivorous theropods may have had dispersals that were less subject to the same climate constraints.

2018 ◽  
Vol 285 (1880) ◽  
pp. 20180361 ◽  
Author(s):  
Martín D. Ezcurra ◽  
Richard J. Butler

One of the key faunal transitions in Earth history occurred after the Permo-Triassic mass extinction ( ca 252.2 Ma), when the previously obscure archosauromorphs (which include crocodylians, dinosaurs and birds) become the dominant terrestrial vertebrates. Here, we place all known middle Permian–early Late Triassic archosauromorph species into an explicit phylogenetic context, and quantify biodiversity change through this interval. Our results indicate the following sequence of diversification: a morphologically conservative and globally distributed post-extinction ‘disaster fauna’; a major but cryptic and poorly sampled phylogenetic diversification with significantly elevated evolutionary rates; and a marked increase in species counts, abundance, and disparity contemporaneous with global ecosystem stabilization some 5 million years after the extinction. This multiphase event transformed global ecosystems, with far-reaching consequences for Mesozoic and modern faunas.


Zootaxa ◽  
2012 ◽  
Vol 3166 (1) ◽  
pp. 1 ◽  
Author(s):  
JULIA B. DESOJO ◽  
MARTÍN D. EZCURRA ◽  
EDIO E. KISCHLAT

We describe the new aetosaur Aetobarbakinoides brasiliensis gen. et sp. nov. from the early Late Triassic (late Carnian-early Norian) Brazilian Santa Maria Formation. The holotype is composed of a partial postcranium including several cer-vical and dorsal vertebrae and ribs, one anterior caudal vertebra, right scapula, right humerus, right tibia, partial right pes,and anterior and mid-dorsal paramedian osteoderms. Aetobarbakinoides is differentiated from other aetosaurs by the pres-ence of cervical vertebrae with widely laterally extended prezygapophyses, mid-cervical vertebrae with anterior articularfacet width more than 1.2 times wider than the posterior one, anterior caudal vertebrae with extremely anteroposteriorlyshort prezygapophyses, elongated humerus and tibia in relation to the axial skeleton, and paramedian osteoderms with aweakly raised anterior bar. A cladistic analysis recovered the new species as more derived than the South American generaAetosauroides (late Carnian-early Norian) and Neoaetosauroides (late Norian-Rhaetian), and it is nested as the sister-tax-on of an unnamed clade, composed of Typothoracisinae and Desmatosuchinae, due to the absence of a ventral keel in thecervical vertebrae. Aetobarbakinoides presents a skeletal anatomy previously unknown among South American aetosaurs,with the combination of presacral vertebrae with hyposphene, anteroposteriorly short and unkeeled cervical vertebrae,gracile limbs, and paramedian osteoderms with a weakly raised anterior bar. Aetobarbakinoides is among the oldest knownaetosaurs together with Aetosauroides from Argentina and Brazil and Stagonolepis robertsoni from Scotland, indicatinga widely distributed early record for the group. In addition, the recognition of a suite of derived features in Aetobarbaki-noides, which is one of the oldest known aetosaurs, is in agreement with an older origin for the group, as it is expected by the extensive ghost lineages at the base of the main pseudosuchian clades.


2021 ◽  
pp. 1-16
Author(s):  
Arymathéia Santos Franco ◽  
Rodrigo Temp Müller ◽  
Agustín G. Martinelli ◽  
Carolina A. Hoffmann ◽  
Leonardo Kerber

Abstract Traversodontidae is a group of Triassic herbivorous/omnivorous cynodonts that represents the most diversified lineage within Cynognathia. In southern Brazil, a rich fossil record of late Middle/mid-Late Triassic cynodonts has been documented, with Exaeretodon riograndensis Abdala, Barberena, and Dornelles, 2002 and Siriusgnathus niemeyerorum Pavanatto et al., 2018 representing two abundant and well-documented traversodontids. The present study provides a comparative analysis of the morphology of the nasal cavity, nasal recesses, nasolacrimal duct, and maxillary canals of both species using computed tomography, highlighting the changes that occurred in parallel to the origin of mammaliaforms. Our results show that there were no ossified turbinals or a cribriform plate delimiting the posterior end of the nasal cavity, suggesting these structures were probably cartilaginous as in nonmammaliaform cynodonts. Both species show lateral ridges on the internal surface of the roof of the nasal cavity, but the median ridge for the attachment of a nasal septum is absent. Exaeretodon riograndensis and S. niemeyerorum show recesses on the dorsal region of the nasal cavity, which increase the volume of the nasal cavity, potentially enhancing the olfactory chamber and contributing to the sense of smell. On the lateral sides of the nasal cavity, the analyzed taxa show a well-developed maxillary recess. Although E. riograndensis and S. niemeyerorum have roughly similar nasal cavities, in the former taxon, the space between the left and right dorsal recesses of the nasal cavity is uniform along its entire extension, whereas this space narrows posteriorly in S. niemeyerorum. Finally, the nasolacrimal duct of S. niemeyerorum is more inclined anteroposteriorly than in E. riograndensis.


Zootaxa ◽  
2010 ◽  
Vol 2374 (1) ◽  
pp. 1 ◽  
Author(s):  
ALLEN L. NORRBOM ◽  
MARTY CONDON

The femoralis species group of the genus Blepharoneura is revised. The following 42 species, including 32 new species, are recognized: amplihyalina, n. sp. (northwestern Argentina), apaapa, n. sp. (Bolivia), aspiculosa, n. sp. (Mexico), bidigitata, n. sp. (southern Brazil), bipunctata, n. sp. (Ecuador), biseriata Wulp (Mexico), bivittata, n. sp. (Nicaragua, Costa Rica), brevivittata, n. sp. (Costa Rica to Peru), chaconi, n. sp. (Costa Rica), cornelli, n. sp. (Costa Rica), cyclantherae, n. sp. (Mexico), femoralis Wulp (Mexico to Brazil), fernandezi, n. sp. (Venezuela, northern Brazil), furcifer Hendel (Venezuela to Bolivia and Brazil), hirsuta Bates (Venezuela, Guyana, Brazil), hyalinella, n. sp. (Bolivia), io Giglio-Tos (Mexico), isolata, n. sp. (Guatemala), lutea, n. sp. (Costa Rica), macwilliamsae, n. sp. (Costa Rica), marshalli, n. sp. (northwestern Argentina), mexicana, n. sp. (Guatemala, Mexico), mikenoltei, n. sp. (Costa Rica), multipunctata, n. sp. (Ecuador), nigriapex, n. sp. (Bolivia), nigrifemur, n. sp. (Bolivia), osmundsonae, n. sp. (Mexico), punctistigma, n. sp. (Mexico to Costa Rica), quadristriata Wulp (Mexico to Costa Rica; possibly Colombia), quetzali, n. sp. (Guatemala), regina Giglio-Tos (Mexico), rupta (Wulp) (Mexico to Costa Rica), ruptafascia, n. sp. (Ecuador), septemdigitata, n. sp. (Peru, Bolivia), sinepuncta, n. sp. (Costa Rica), splendida Giglio-Tos (Mexico to Ecuador), tau, n. sp. (Costa Rica), thetis Hendel (southern Brazil), unifasciata, n. sp. (Ecuador), variabilis, n. sp. (Mexico), wasbaueri, n. sp. (Ecuador), and zumbadoi, n. sp. (Costa Rica). Blepharoneura amazonensis Lima & Leite, 1952 is considered a new synonym of B. hirsuta Bates, 1933, and a lectotype is designated for Blepharoneura furcifer Hendel, 1914. A key to species and phylogenetic analysis are provided, as well as descriptions, illustrations, distributions, and host plant data (as available) for each species.


2019 ◽  
pp. 1-9 ◽  
Author(s):  
Paulo R. Romo-de-Vivar-Martínez ◽  
Agustín G. Martinelli ◽  
Voltaire D. Paes Neto ◽  
Camila A. Scartezini ◽  
Marcel B. Lacerda ◽  
...  

2020 ◽  
Vol 18 (13) ◽  
pp. 1103-1126 ◽  
Author(s):  
Paulo R. Romo de Vivar ◽  
Agustín G. Martinelli ◽  
Annie Schmaltz Hsiou ◽  
Marina Bento Soares

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