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   » » Wiki: Archosauriformes
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Archosauriformes ( for 'ruling lizards', and for 'form') is a of encompassing and some of their close relatives. It was defined by (1994) as the clade stemming from the last common ancestor of and Archosauria.Gauthier J. A. (1994): The diversification of the amniotes. In: D. R. Prothero and R. M. Schoch (ed.) Major Features of Vertebrate Evolution: 129-159. Knoxville, Tennessee: The Paleontological Society. (2005) defined it as the most exclusive clade containing and Archosauria. Gauthier as part of the (2020) defined the clade as the last common ancestor of , , and , and all its descendants.

(2025). 9780429446276, CRC Press. .
Archosauriforms are a branch of which originated in the (roughly 252 million years ago) and persist to the present day as the two surviving archosaur groups: and .

Archosauriforms present several traits historically ascribed to the group Archosauria. These include serrated teeth set in deep sockets, a more active metabolism, and an antorbital fenestra (a hole in the skull in front of the eyes). Reptiles with these traits have also been termed "" in older methods of classification. Thecodontia is a group, and its usage as a category has been rejected under modern systems. The name Archosauriformes is intended as a replacement compatible with modern taxonomy.


Evolutionary history
Early archosauriforms, informally termed "", were superficially crocodile-like animals with sprawling gaits, carnivorous habits, and long hooked snouts. Unlike the bulk of their contemporaries, archosauriforms survived the catastrophic end-Permian mass extinction. The Late Permian proterosuchid is similar in appearance to its relative, Proterosuchus. Within a few million years after the beginning of the , the archosauriformes had diversified past the "proterosuchian" grade. The next major archosauriform group was , a family of with massive heads, the largest terrestrial carnivorous reptiles up to that time.

In 2016, provided the name Eucrocopoda for the clade including all archosauriforms more (closer to archosaurs) than erythrosuchids. He defined the clade all taxa more closely related to Euparkeria capensis, , Doswellia kaltenbachi, Parasuchus hislopi, Passer domesticus (the house sparrow), or Crocodylus niloticus (the Nile crocodile) than to Proterosuchus fergusi or Erythrosuchus africanus. The name translates to "true crocodile feet", in reference to the possession of a crocodilian-style . Eucrocopodans include the families (small, agile reptiles),Proterochampsidae (narrow-snouted predators endemic to ), and (heavily armored reptiles similar to proterochampsids), as well as various other strange reptiles such as and .

The most successful archosauriforms, and the only members to survive into the , were the . Archosauria includes crocodilians, birds, and all descendants of their . Extinct archosaurs include , (both members of the crocodilian branch), , and non-avian (both members of the avian branch). Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and Their Kin


Metabolism
Vascular density and density, shape and area have been used to estimate the bone growth rate of archosaurs, leading to the conclusion that this rate had a tendency to grow in ornithodirans and decrease in pseudosuchians. The same method also supports the existence of high resting metabolical rates similar to those of living endotherms (mammals and birds) in the -Archosauriformes clade that were retained by most subgroups, though decreased in Proterosuchus, and Crocodilia. Erythrosuchids and Euparkeria are basal archosauriforms showing signs of high growth rates and elevated metabolism, with Erythrosuchus possessing a rate similar of the fastest-growing dinosaurs. Sexual maturity in those Triassic taxa was probably reached quickly, providing advantage in a habitat with unpredictable variation from heavy rainfall to drought and high mortality. and Euparkeria, which show slower growth rates compared to Erythrosuchus, lived after the climatic stabilization. Early crown archosaurs possessed increased growth rates, which were retained by ornithodirans. and are stem-crocodilians that show high growth rates similar to those of basal archosauriforms.

Developmental, physiological, anatomical and palaeontological lines of evidence indicate that crocodilians evolved from endothermic ancestors. Living crocodilians are ambush predators adapted to a semi-aquatic lifestyle that benefits from ectothermy due to the lower oxygen intake that allows longer diving time. The mixing of oxygenated and deoxygenated blood in their circulatory system is apparently an innovation that benefits ectothermic life. Earlier archosaurs likely lacked those adaptations and instead had completely separated blood as birds and mammals do. A similar process occurred in phytosaurs, which were also semi-aquatic.

The similarities between , and integument suggest a common origin of thermal insulation (feathers) in ornithodirans at least 250 million years ago. Erythrosuchids living in high latitudes might have benefited from some sort of insulation. If was an archosauromorph, it could be associated with the origin of feathers.


Relationships
Below is a cladogram from Nesbitt (2011):

Below is a cladogram from Sengupta et al. (2017), based on an updated version of Ezcurra (2016) that reexamined all historical members of the "Proterosuchia" (a historical group including and ). The placement of fragmentary taxa that had to be removed to increase tree resolution are indicated by dashed lines (in the most derived position that they can be confidently assigned to). Taxa that are are indicated by the note "dubium". Bold terminal taxa are collapsed.


Sources
  • (1986). 9780940228146, California Academy of Sciences.


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