Amniote

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Amniotes Temporal range: Late Carboniferous–Present[1] PreꞒ Ꞓ O S D C P T J K Pg N (Possible Mississippian record)
From top to bottom and left to right, examples of amniotes: Edaphosaurus, red fox (two synapsids), king cobra and a white-headed buffalo weaver (two sauropsids).
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Chordata
Superclass:	Tetrapoda
Clade:	Reptiliomorpha
Clade:	Amniota Haeckel, 1866
Clades
Synapsida Sauropsida incertae sedis †Casineria?[2] †Kraterokheirodon[3] †Diadectomorpha? †Varanopidae

Amniotes are tetrapod vertebrate animals belonging to the clade Amniota, a large group that comprises the vast majority of living terrestrial and semiaquatic vertebrates. Amniotes evolved from amphibious stem tetrapod ancestors during the Carboniferous period. Those of Amniota are defined as the smallest crown clade containing humans, the Greek tortoise, and the Nile crocodile.^[4][5]

Amniotes are distinguished from the other living tetrapod clade — the non-amniote lissamphibians (frogs, salamanders, and caecilians) — by the development of three extraembryonic membranes (amnion for embryonic protection, chorion for gas exchange, and allantois for metabolic waste disposal or storage), thicker and keratinized skin, costal respiration (breathing by expanding/constricting the rib cage), the presence of adrenocortical and chromaffin tissues as a discrete pair of glands near their kidneys, more complex kidneys, the presence of an astragalus for better extremity range of motion, the diminished role of skin breathing, and the complete loss of metamorphosis, gills, and lateral lines.^{[6][7][8][9][10]: 600  [10]: 552 [11] [10]: 694}

The presence of an amniotic buffer, of a water-impermeable skin, and of a robust, air-breathing, respiratory system, allow amniotes to live on land as true terrestrial animals. Amniotes have the ability to procreate without water bodies. Because the amnion and the fluid it secretes shields the embryo from environmental fluctuations, amniotes can reproduce on dry land by either laying shelled eggs (reptiles, birds and monotremes) or nurturing fertilized eggs within the mother (marsupial and placental mammals). This distinguishes amniotes from anamniotes (fish and amphibians) that have to spawn in aquatic environments. Most amniotes still require regular access to drinking water for rehydration, like the semiaquatic amphibians do.

They have better homeostasis in drier environments, and more efficient non-aquatic gas exchange to power terrestrial locomotion, which is facilitated by their astragalus.

Basal amniotes resembled small lizards and evolved from semiaquatic reptiliomorphs during the Carboniferous period.^[12] After the Carboniferous rainforest collapse, amniotes spread around Earth's land and became the dominant land vertebrates.^[12]

They almost immediately diverged into two groups, namely the sauropsids (including all reptiles and birds) and synapsids (including mammals and extinct ancestors like "pelycosaurs" and therapsids). Among the earliest known crown group amniotes, the oldest known sauropsid is Hylonomus and the oldest known synapsid is Asaphestera, both of which are from Nova Scotia during the Bashkirian age of the Late Carboniferous around 318 million years ago.^[1][13]

This basal divergence within Amniota has also been dated by molecular studies at 310–329 Ma,^[14] or 312–330 Ma,^[15] and by a fossilized birth–death process study at 322–340 Ma.^[16]

The term amniote comes from the amnion, which derives from Greek ἀμνίον (amnion), which denoted the membrane that surrounds a fetus. The term originally described a bowl in which the blood of sacrificed animals was caught, and derived from ἀμνός (amnos), meaning "lamb".^[17]

Zoologists characterize amniotes in part by embryonic development that includes the formation of several extensive membranes, the amnion, chorion, and allantois. Amniotes develop directly into a (typically) terrestrial form with limbs and a thick stratified epithelium (rather than first entering a feeding larval tadpole stage followed by metamorphosis, as amphibians do). In amniotes, the transition from a two-layered periderm to a cornified epithelium is triggered by thyroid hormone during embryonic development, rather than by metamorphosis.^[18] The unique embryonic features of amniotes may reflect specializations for eggs to survive drier environments; or the increase in size and yolk content of eggs may have permitted, and coevolved with, direct development of the embryo to a large size.

Features of amniotes evolved for survival on land include a sturdy but porous leathery or hard eggshell and an allantois that facilitates respiration while providing a reservoir for disposal of wastes. Their kidneys (metanephros) and large intestines are also well-suited to water retention. Most mammals do not lay eggs, but corresponding structures develop inside the placenta.

The ancestors of true amniotes, such as Casineria kiddi, which lived about 340 million years ago, evolved from amphibian reptiliomorphs and resembled small lizards. At the late Devonian mass extinction (360 million years ago), all known tetrapods were essentially aquatic and fish-like. Because the reptiliomorphs were already established 20 million years later when all their fishlike relatives were extinct, it appears they separated from the other tetrapods somewhere during Romer's gap, when the adult tetrapods became fully terrestrial (some forms would later become secondarily aquatic).^[19] The modest-sized ancestors of the amniotes laid their eggs in moist places, such as depressions under fallen logs or other suitable places in the Carboniferous swamps and forests; and dry conditions probably do not account for the emergence of the soft shell.^[20] Indeed, many modern-day amniotes require moisture to keep their eggs from desiccating.^[21] Although some modern amphibians lay eggs on land, all amphibians lack advanced traits like an amnion.

The amniotic egg formed through a series of evolutionary steps. After internal fertilization and the habit of laying eggs in terrestrial environments became a reproduction strategy amongst the amniote ancestors, the next major breakthrough appears to have involved a gradual replacement of the gelatinous coating covering the amphibian egg with a fibrous shell membrane. This allowed the egg to increase both its size and in the rate of gas exchange, permitting a larger, metabolically more active embryo to reach full development before hatching. Further developments, like extraembryonic membranes (amnion, chorion, and allantois) and a calcified shell, were not essential and probably evolved later.^[22] It has been suggested that shelled terrestrial eggs without extraembryonic membranes could still not have been more than about 1 cm (0.4-inch) in diameter because of diffusion problems, like the inability to get rid of carbon dioxide if the egg was larger. The combination of small eggs and the absence of a larval stage, where posthatching growth occurs in anamniotic tetrapods before turning into juveniles, would limit the size of the adults. This is supported by the fact that extant squamate species that lay eggs less than 1 cm in diameter have adults whose snout-vent length is less than 10 cm. The only way for the eggs to increase in size would be to develop new internal structures specialized for respiration and for waste products. As this happened, it would also affect how much the juveniles could grow before they reached adulthood.^[23]

A similar pattern can be seen in modern amphibians. Frogs that have evolved terrestrial reproduction and direct development have both smaller adults and fewer and larger eggs compared to their relatives that still reproduce in water.^[24]

Fish and amphibian eggs have only one inner membrane, the embryonic membrane. Evolution of the amniote egg required increased exchange of gases and wastes between the embryo and the atmosphere. Structures to permit these traits allowed further adaption that increased the feasible size of amniote eggs and enabled breeding in progressively drier habitats. The increased size of eggs permitted increase in size of offspring and consequently of adults. Further growth for the latter, however, was limited by their position in the terrestrial food-chain, which was restricted to level three and below, with only invertebrates occupying level two. Amniotes would eventually experience adaptive radiations when some species evolved the ability to digest plants and new ecological niches opened up, permitting larger body-size for herbivores, omnivores and predators.^{[citation needed]}

While the early amniotes resembled their amphibian ancestors in many respects, a key difference was the lack of an otic notch at the back margin of the skull roof. In their ancestors, this notch held a spiracle, an unnecessary structure in an animal without an aquatic larval stage.^[25] There are three main lines of amniotes, which may be distinguished by the structure of the skull and in particular the number of holes behind each eye. In anapsids, the ancestral condition, there are none; in synapsids (mammals and their extinct relatives) there is one; and in diapsids (including birds, crocodilians, squamates, and tuataras), there are two. Turtles have secondarily lost their fenestrae, and were traditionally classified as anapsids because of this. Molecular testing firmly places them in the diapsid line of descent.

Post-cranial remains of amniotes can be identified from their labyrinthodont ancestors by their having at least two pairs of sacral ribs, a sternum in the pectoral girdle (some amniotes have lost it) and an astragalus bone in the ankle.^[26]

Amniota was first formally described by the embryologist Ernst Haeckel in 1866 on the presence of the amnion, hence the name. A problem with this definition is that the trait (apomorphy) in question does not fossilize, and the status of fossil forms has to be inferred from other traits.

Amniotes

Archaeothyris, one of the most basal synapsids, first appears in the fossil records about 306 million years ago.^[27]

By the Mesozoic, 150 million years ago, sauropsids included the largest animals anywhere. Shown are some late Jurassic dinosaurs, including the early bird Archaeopteryx perched on a tree stump.

Older classifications of the amniotes traditionally recognised three classes based on major traits and physiology:^{[28][29][30][31]}

• Class Reptilia (reptiles)
  • Subclass Anapsida ("proto-reptiles", possibly including turtles)
  • Subclass Diapsida (majority of reptiles,^[32] progenitors of birds)
  • Subclass Euryapsida (plesiosaurs, placodonts, and ichthyosaurs)
  • Subclass Synapsida (stem or proto-mammals, progenitors of mammals)
• Class Aves (birds)
  • Subclass Archaeornithes (reptile-like birds, progenitors of all other birds)
  • Subclass Enantiornithes (early birds with an alternative shoulder joint)^[33]
  • Subclass Hesperornithes (toothed aquatic flightless birds)
  • Subclass Ichthyornithes (toothed, but otherwise modern birds)
  • Subclass Neornithes (all living birds)
• Class Mammalia (mammals)
  • Subclass Prototheria (Monotremata, egg-laying mammals)
  • Subclass Theria (Metatheria (such as marsupials) and Eutheria (such as placental mammals))

This rather orderly scheme is the one most commonly found in popular and basic scientific works. It has come under critique from cladistics, as the class Reptilia is paraphyletic—it has given rise to two other classes not included in Reptilia.

Most species described as microsaurs, formerly grouped in the extinct and prehistoric amphibian group lepospondyls, has been placed in the newer clade Recumbirostra, and shares many anatomical features with amniotes which indicates they were amniotes themselves.^[34]

A different approach is adopted by writers who reject paraphyletic groupings. One such classification, by Michael Benton, is presented in simplified form below.^[35]

• Series Amniota
  • (Class) Clade Synapsida
    • A series of unassigned families, corresponding to Pelycosauria †
    • (Order) Clade Therapsida
      • Class Mammalia – mammals
  • (Class) Clade Sauropsida
    • Subclass Parareptilia †
      • Family Mesosauridae †
      • Family Millerettidae †
      • Family Bolosauridae †
      • Family Procolophonidae †
      • Order Pareiasauromorpha
        • Family Nycteroleteridae †
        • Family Pareiasauridae †
    • (Subclass) Clade Eureptilia
      • Family Captorhinidae †
      • (Infraclass) Clade Diapsida
        • Family Araeoscelididae †
        • Family Weigeltisauridae †
        • Order Younginiformes †
        • (Infraclass) Clade Neodiapsida
          • Order Testudinata
            • Suborder Testudines – turtles
          • Infraclass Lepidosauromorpha
            • Unnamed infrasubclass
              • Infraclass Ichthyosauria †
              • Order Thalattosauria †
              • Superorder Lepidosauriformes
                • Order Sphenodontida – tuatara
                • Order Squamata – lizards and snakes
            • Infrasubclass Sauropterygia †
              • Order Placodontia †
              • Order Eosauropterygia †
                • Suborder Pachypleurosauria †
                • Suborder Nothosauria †
              • Order Plesiosauria †
          • (Infraclass) Clade Archosauromorpha
            • Family Trilophosauridae †
            • Order Rhynchosauria †
            • Order Protorosauria †
            • Division Archosauriformes
              • Subdivision Archosauria
                • Infradivision Crurotarsi
                  • Order Phytosauria†
                  • Family Ornithosuchidae †
                  • Family Stagonolepididae †
                  • Family Rauisuchidae †
                  • Superfamily Poposauroidea †
                  • Superorder Crocodylomorpha
                    • Order Crocodylia – crocodilians
                • Infradivision Avemetatarsalia
                  • Infrasubdivision Ornithodira
                    • Order Pterosauria †
                    • Family Lagerpetidae †
                    • Family Silesauridae †
                    • (Superorder) Clade Dinosauria – dinosaurs
                      • Order Ornithischia †
                      • (Order) Clade Saurischia
                        • (Suborder) Clade Theropoda – theropods
                          • Class Aves – birds

With the advent of cladistics, other researchers have attempted to establish new classes, based on phylogeny, but disregarding the physiological and anatomical unity of the groups. Unlike Benton, for example, Jacques Gauthier and colleagues forwarded a definition of Amniota in 1988 as "the most recent common ancestor of extant mammals and reptiles, and all its descendants".^[26] As Gauthier makes use of a crown group definition, Amniota has a slightly different content than the biological amniotes as defined by an apomorphy.^[36] Though traditionally considered reptiliomorphs, some recent research has recovered diadectomorphs as the sister group to Synapsida within Amniota, based on inner ear anatomy.^[37][38][39]

The cladogram presented here illustrates the phylogeny (family tree) of amniotes, and follows a simplified version of the relationships found by Laurin & Reisz (1995),^[40] with the exception of turtles, which more recent morphological and molecular phylogenetic studies placed firmly within diapsids.^{[41][42][43][44][45][46]} The cladogram covers the group as defined under Gauthier's definition.

Following studies in 2022 and 2023,^[47][48] with Drepanosauromorpha placed sister to Weigeltisauridae (Coelurosauravus) in Avicephala based on Senter (2004):^[49]