Information about Archosaurs
| Archosaurs Fossil range: Early Triassic - Recent | ||||||||||||
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Living archosaurs include crocodiles (pictured above) and birds. Living archosaurs include crocodiles (pictured above) and birds. | ||||||||||||
| Scientific classification | ||||||||||||
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| Clades | ||||||||||||
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There is some debate about when archosaurs first appeared. Those who classify the Permian reptiles Archosaurus rossicus and / or Protorosaurus speneri as true archosaurs maintain that archosaurs first appeared in the late Permian. Those who classify both Archosaurus rossicus and Protorosaurus speneri as archosauriformes (not true archosaurs but very closely related) maintain that archosaurs first evolved from Archosauriform ancestors during the Olenekian (early Triassic Period).
Distinguishing characteristics
The simplest and most widely-agreed synapomorphies of archosaurs are:- Teeth set in sockets, which makes them less likely to be torn loose during feeding. This feature is responsible for the name "thecodonts" ("socket teeth"), which paleontologists used to apply to all or most archosaurs.
- Preorbital fenestrae (openings in the skull in front of the eyes but behind the nostrils), which reduced the weight of the skull, a useful feature since most early archosaurs had long, heavy skulls, rather like those of modern crocodilians. The preorbital fenestrae (sometimes called anteorbital fenestrae) are often larger than the orbits (eye sockets).
- Mandibular fenestrae (small openings in the jaw bones), which may have reduced the weight of the jaw slightly.
- A fourth trochanter (ridge for attaching muscles) on the femur. This seemingly insignificant detail may have made the evolution of dinosaurs possible (all early dinosaurs and many later ones were bipeds), and may also be connected with the ability of the archosaurs or their immediate ancestors to survive the catastrophic Permian-Triassic extinction event.
Archosaur takeover in the Triassic
Mammal-like reptiles were the dominant land vertebrates throughout the Permian, but most perished in the Permian-Triassic extinction event. Lystrosaurus (a herbivorous mammal-like reptile) was the only large land animal to survive the event, becoming the most populous land animal on the planet for a time.[1]But archosaurs quickly became the dominant land vertebrates in the early Triassic. The two most commonly-suggested explanations for this are:
- Archosaurs made quicker progress than mammal-like reptiles towards erect limbs, and this gave them greater stamina by avoiding Carrier's constraint. This is unconvincing since Archosaurs became dominant while they still had sprawling or semi-erect limbs, similar to those of Lystrosaurus and other mammal-like reptiles.
- The early Triassic was predominantly arid, because most of the earth's land was concentrated in the supercontinent Pangaea. Archosaurs were probably better at conserving water than mammal-like reptiles:
Modern diapsids (lizards, snakes, crocodilians, birds) excrete uric acid, which can be excreted as a paste. It is reasonable to suppose that archosaurs (diapsids and ancestors of crocodilians, dinosaurs and birds) also excreted uric acid, and therefore were good at conserving water. The aglandular (glandless) skins of diapsids would also have helped to conserve water.
Modern mammals excrete urea, which requires a lot of water to keep it dissolved. Their skins also contain many glands, which also lose water. Assuming that mammal-like reptiles had similar features, as argued e.g. in Palaeos http://www.palaeos.com/Vertebrates/Units/270Archosauromorpha/270.000.html, they were at a disadvantage in a mainly arid world. The same well-respected site points out that "for much of Australia's Plio-Pleistocene history, where conditions were probably similar, the largest terrestrial predators were not mammals but gigantic varanid lizards (Megalania) and land crocs."
Main types of archosaurs
Since the 1970s scientists have classified archosaurs mainly on the basis of their ankles.[2] The earliest archosaurs had "primitive mesotarsal" ankles: the astragalus and calcaneum were fixed to the tibia and fibula by sutures and the joint bent about the contact between these bones and the foot.
Crocodilian form of crurotarsal ankle. Adapted with permission from Palaeos

Reversed crurotarsal ankle. Adapted with permission from Palaeos

"Advanced" mesotarsal ankle. Adapted with permission from Palaeos
Hip joints and locomotion
Like the early tetrapods, early archosaurs had a sprawling gait because:- Their hip sockets faced sideways.
- The knobs at the tops of their femurs were in line with the femur.
- The hip sockets faced sideways but the knobs on the femurs were at right angles to the rest of the femur, which therefore pointed downwards. Dinosaurs evolved from archosaurs with this hip arrangement.
- The hip sockets faced downwards and the knobs on the femurs were in line with the femur. This "pillar-erect" arrangement appears to evolved more than once independently in various archosaur lineages, for example it was common in Rauisuchia and also appeared in some aetosaurs.
Extinction and survival
Crocodilians, pterosaurs, dinosaurs, and champsosaurs survived the Triassic-Jurassic extinction event about 195 million years ago, but other archosaurs became extinct.Non-avian dinosaurs and pterosaurs perished in the Cretaceous-Tertiary extinction event, but crocodilians, champsosaurs, and birds (last suviving dinosaur group) survived. Birds are descendants of archosaurs, and are therefore archosaurs themselves under phylogenetic taxonomy.
Champsosaurs became extinct in the Oligocene.
Crocodilians (which include all modern crocodiles, alligators, and gharials) and birds flourish today, and it is generally agreed that birds have the most species of all air-breathing vertebrates.
Archosaur lifestyle
Diet
Most were large predators, but members of various lines diversified into other niches:- aetosaurs were herbivores and some developed spectacular armor.
- A few crocodilians were herbivores, e.g. Simosuchus.
- The large crocodilian Stomatosuchus may have been a filter feeder.
Land, water and air
Archosaurs are mainly portrayed as land animals, but:- The crocodilians dominated the rivers and swamps and even invaded the seas (the Teleosaurs and Metriorhynchidae). The Metriorhynchidae were rather dolphin-like, with paddle-like forelimbs, a tail fluke and smooth, unarmoured skins.
- Their descendants the pterosaurs and the birds dominated the air.
Metabolism
The metabolism of archosaurs is still a controversial topic. They certainly evolved from cold-blooded ancestors, and the surviving non-dinosaurian archosaurs, crocodilians, are cold-blooded. But crocodilians have some features which are normally associated with a warm-blooded metabolism because they improve the animal's oxygen supply:- 4-chambered hearts. Mammals and birds have 4-chambered hearts. Non-crocodilian reptiles have 3-chambered hearts, which are less efficient because they allow oxygenated and de-oxygenated blood to mix and therefore send some de-oxygenated blood out to the body instead of to the lungs. Modern crocodilians' hearts are 4-chambered, but are smaller relative to body size and run at lower pressure than those of modern mammals and birds. They also have a bypass which makes them functionally 3-chambered when under water, conserving oxygen.
- a secondary palate, which allows the animal to eat and breathe at the same time.
- a hepatic piston mechanism for pumping the lungs. This is different from the lung-pumping mechanisms of mammals and birds but similar to what some researchers claim to have found in some dinosaurs.[4][5]
Some experts believe that crocodilians were originally active, warm-blooded predators and that their archosaur ancestors were warm-blooded. Developmental studies indicate that crocodilian embryos develop fully 4-chambered hearts first and then develop the modifications which make their hearts function as 3-chambered under water. Using the principle that ontogeny recapitulates phylogeny, the researchers concluded that the original crocodilians had fully 4-chambered hearts and were therefore warm-blooded and that later crocodilians developed the bypass as they reverted to being cold-blooded aquatic ambush predators. [6][7]
If the original crocodilians were warm-blooded and other "crurotarsan" archosaurs were also warm-blooded, this would help to resolve some evolutionary puzzles:
- The earliest crocodilians, e.g. Terrestrisuchus, were slim, leggy terrestrial predators whose build suggests a fairly active lifestyle, which requires a fairly fast metabolism. And some other "crurotarsan" archosaurs appear to have had erect limbs, while those of rauisuchians are very poorly adapted for any other posture. Erect limbs are advantageous for active animals because they avoid Carrier's constraint, but disavantageous for more sluggish animals because they increase the energy costs of standing up and lying down.
- If early archosaurs were completely cold-blooded and (as seems most likely) dinosaurs were at least fairly warm-blooded, dinosaurs would have had to evolve warm-blooded metabolisms in less than half the time it took for mammal-like reptiles to do the same.
Phylogeny
Avesuchia `--ArchosauriaCrurotarsi | |-?Ctenosauriscidae | `--Crocodylotarsi | |--Ornithosuchidae | `--+--Phytosauria | `--Suchia | |--Prestosuchidae | `--Rauisuchiformes | |--Aetosauria | `--Rauisuchia | |--Rauisuchidae | `--+--Paracrocodylomorpha | `--Crocodylomorpha (crocodiles and relatives) `--OrnithodiraPterosauromorpha | |--Scleromochlus | `--Pterosauria `--Dinosauromorpha `--Dinosauriformes `--DinosauriaOrnithischia `--Saurischia `--Aves (birds)References
1. ^ Before the Dinosaurs, Discovery Channel
2. ^ Archosauromorpha: Archosauria - Palaeos
3. ^ Archosauromorpha: overview Palaeos
4. ^ Ruben, J., et al (1996). "The metabolic status of some Late Cretaceous dinosaurs". Science (273): 120-147.
5. ^ Ruben, J., et al (1997). "Lung structure and ventilation in theropod dinosaurs and early birds". Science (278): 1267-1247.
6. ^ Seymour, R. S., Bennett-Stamper, C. L., Johnston, S. D., Carrier, D. R. and Grigg, G. C. (2004). "Evidence for endothermic ancestors of crocodiles at the stem of archosaur evolution". Physiol. Biochem. Zool. 77: 1051-1067.
7. ^ Summers, A.P. (2005). "Evolution: Warm-hearted crocs". Nature 434: 833-834.
2. ^ Archosauromorpha: Archosauria - Palaeos
3. ^ Archosauromorpha: overview Palaeos
4. ^ Ruben, J., et al (1996). "The metabolic status of some Late Cretaceous dinosaurs". Science (273): 120-147.
5. ^ Ruben, J., et al (1997). "Lung structure and ventilation in theropod dinosaurs and early birds". Science (278): 1267-1247.
6. ^ Seymour, R. S., Bennett-Stamper, C. L., Johnston, S. D., Carrier, D. R. and Grigg, G. C. (2004). "Evidence for endothermic ancestors of crocodiles at the stem of archosaur evolution". Physiol. Biochem. Zool. 77: 1051-1067.
7. ^ Summers, A.P. (2005). "Evolution: Warm-hearted crocs". Nature 434: 833-834.
Further reading
- Benton, M. J. (2004), Vertebrate Paleontology, 3rd ed. Blackwell Science Ltd
- Carroll, R. L. (1988), Vertebrate Paleontology and Evolution, W. H. Freeman and Co. New York
External links
- UCMP
- Paleos reviews the messy history of archosaur phylogeny (family tree) and has an excellent image of the various archosaur ankle types.
- Mikko's Phylogeny Archive Archosauria
The Early Triassic (also known as Lower Triassic, Buntsandstein, or Scythian) is the first of three epochs of the Triassic period. It spans the time between 251 ± 0.4 Ma and 245 ± 1.5 Ma (million years ago).
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Crocodylidae
Cuvier, 1807
Genera
A crocodile is any species belonging to the family Crocodylidae
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Cuvier, 1807
Genera
- Mecistops
- Crocodylus
- Osteolaemus
A crocodile is any species belonging to the family Crocodylidae
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Aves
Linnaeus, 1758
Orders
About two dozen - see section below
Birds (class Aves) are bipedal, warm-blooded, egg-laying vertebrate animals.
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Linnaeus, 1758
Orders
About two dozen - see section below
Birds (class Aves) are bipedal, warm-blooded, egg-laying vertebrate animals.
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Scientific classification or biological classification is a method by which biologists group and categorize species of organisms. Scientific classification also can be called scientific taxonomy, but should be distinguished from folk taxonomy, which lacks scientific basis.
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Chordata
Bateson, 1885
Typical Classes
See below
Chordates (phylum Chordata) are a group of animals that includes the vertebrates, together with several closely related invertebrates.
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Bateson, 1885
Typical Classes
See below
Chordates (phylum Chordata) are a group of animals that includes the vertebrates, together with several closely related invertebrates.
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Sauropsida*
Goodrich, 1916
Subclasses
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Goodrich, 1916
Subclasses
- Anapsida
- Diapsida
- Reptilia Laurenti, 1768
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Diapsida
Osborn, 1903
Groups
See text
Diapsids ("two arches") are a group of tetrapod animals that developed two holes (temporal fenestra) in each side of their skulls, about 300 million years ago during the late Carboniferous period.
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Osborn, 1903
Groups
See text
Diapsids ("two arches") are a group of tetrapod animals that developed two holes (temporal fenestra) in each side of their skulls, about 300 million years ago during the late Carboniferous period.
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Archosauromorpha
von Huene, 1946
Orders
See text
Archosauromorpha (Greek for "ruling lizard forms") is an Infraclass of diapsid reptiles that first appeared during the late Permian and became more common during the Triassic.
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von Huene, 1946
Orders
See text
Archosauromorpha (Greek for "ruling lizard forms") is an Infraclass of diapsid reptiles that first appeared during the late Permian and became more common during the Triassic.
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Edward Drinker Cope (July 28, 1840–April 12, 1897) was an American paleontologist and comparative anatomist, as well as a noted herpetologist and ichthyologist.
Cope was born in Philadelphia to Quaker parents.
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Cope was born in Philadelphia to Quaker parents.
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Crurotarsi
Sereno & Arcucci, 1990
Orders
The Crurotarsi ("cross-ankles") are a group of archosaurs created as a node-based clade by Paul Sereno in 1991 to supplant the old term
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Sereno & Arcucci, 1990
Orders
- Phytosauria
- Aetosauria
- Rauisuchia*
- Crocodilia
The Crurotarsi ("cross-ankles") are a group of archosaurs created as a node-based clade by Paul Sereno in 1991 to supplant the old term
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Aetosauria
Lydekker, 1889
Family: Stagonolepididae
Lydekker, 1887
Genera
Acaenasuchus
Aetosauroides
Aetosaurus
Argentinosuchus
''Calyptosuchus
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Lydekker, 1889
Family: Stagonolepididae
Lydekker, 1887
Genera
Acaenasuchus
Aetosauroides
Aetosaurus
Argentinosuchus
''Calyptosuchus
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Crocodilia
Owen, 1842
Families
Crocodilia
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Owen, 1842
black: range of Crocodilia
Families
- Gavialidae
- Alligatoridae
- Crocodylidae
Crocodilia
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Phytosauria
von Meyer, 1861
Family: Phytosauridae
Jaeger, 1828
Genera
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von Meyer, 1861
Family: Phytosauridae
Jaeger, 1828
Genera
- ?Centemodon
- Paleorhinus
- Angistorhinus
- Brachysuchus
- Smilosuchus
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Rauisuchia*
von Huene, 1942
Families
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von Huene, 1942
Families
- Family Prestosuchidae
- Family Rauisuchidae
- Family Poposauridae
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Ornithodira
Gauthier, 1986
Clades
Ornithodira is a clade within the larger group Archosauria. Another name for this group is Avemetatarsalia.
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Gauthier, 1986
Clades
- Dinosauromorpha
- Pterosauromorpha
Ornithodira is a clade within the larger group Archosauria. Another name for this group is Avemetatarsalia.
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Aves
Linnaeus, 1758
Orders
About two dozen - see section below
Birds (class Aves) are bipedal, warm-blooded, egg-laying vertebrate animals.
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Linnaeus, 1758
Orders
About two dozen - see section below
Birds (class Aves) are bipedal, warm-blooded, egg-laying vertebrate animals.
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Dinosauria *
Owen, 1842
Orders & Suborders
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Owen, 1842
Orders & Suborders
- Ornithischia
- Cerapoda
- Thyreophora
- Saurischia
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Pterosauria
Kaup, 1834
Suborders
Pterodactyloidea
Rhamphorhynchoidea *
Pterosaurs (/ˈtɛ.
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Kaup, 1834
Suborders
Pterodactyloidea
Rhamphorhynchoidea *
Pterosaurs (/ˈtɛ.
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Ancient Greek refers to the second stage in the history of the Greek language[1] as it existed during the Archaic (9th–6th centuries BC) and Classical (5th–4th centuries BC) periods in Greece.
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Diapsida
Osborn, 1903
Groups
See text
Diapsids ("two arches") are a group of tetrapod animals that developed two holes (temporal fenestra) in each side of their skulls, about 300 million years ago during the late Carboniferous period.
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Osborn, 1903
Groups
See text
Diapsids ("two arches") are a group of tetrapod animals that developed two holes (temporal fenestra) in each side of their skulls, about 300 million years ago during the late Carboniferous period.
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Sauropsida*
Goodrich, 1916
Subclasses
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Goodrich, 1916
Subclasses
- Anapsida
- Diapsida
- Reptilia Laurenti, 1768
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Aves
Linnaeus, 1758
Orders
About two dozen - see section below
Birds (class Aves) are bipedal, warm-blooded, egg-laying vertebrate animals.
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Linnaeus, 1758
Orders
About two dozen - see section below
Birds (class Aves) are bipedal, warm-blooded, egg-laying vertebrate animals.
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Crocodilia
Owen, 1842
Families
Crocodilia
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Owen, 1842
black: range of Crocodilia
Families
- Gavialidae
- Alligatoridae
- Crocodylidae
Crocodilia
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Dinosauria *
Owen, 1842
Orders & Suborders
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Owen, 1842
Orders & Suborders
- Ornithischia
- Cerapoda
- Thyreophora
- Saurischia
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Permian is a geologic period that extends from about 299.0 ± 0.8 Ma to 251.0 ± 0.4 Ma (million years before the present; ICS 2004). It is the last period of the Paleozoic Era.
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'Archosauriformes
Gauthier, 1986
Groups
Proterosuchidae
Erythrosuchidae
Euparkeriidae
Archosauria
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Gauthier, 1986
Groups
Proterosuchidae
Erythrosuchidae
Euparkeriidae
Archosauria
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'Archosauriformes
Gauthier, 1986
Groups
Proterosuchidae
Erythrosuchidae
Euparkeriidae
Archosauria
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Gauthier, 1986
Groups
Proterosuchidae
Erythrosuchidae
Euparkeriidae
Archosauria
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The Olenekian (also known as the Yongningzhenian) is a stage of the Early Triassic epoch. It spans the time between 249.7 ± 0.7 Ma and 245 ± 0.7 Ma (million years ago).
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