Evolution of tetrapods

The evolution of tetrapods began about 400 million years ago in the Devonian Period with the earliest tetrapods evolved from lobe-finned fishes.[1] Tetrapods (under the apomorphy-based definition used on this page) are categorized as animals in the biological superclass Tetrapoda, which includes all living and extinct amphibians, reptiles, birds, and mammals. While most species today are terrestrial, little evidence supports the idea that any of the earliest tetrapods could move about on land, as their limbs could not have held their midsections off the ground and the known trackways do not indicate they dragged their bellies around. Presumably, the tracks were made by animals walking along the bottoms of shallow bodies of water.[2] The specific aquatic ancestors of the tetrapods, and the process by which land colonization occurred, remain unclear, and are areas of active research and debate among palaeontologists at present.

See also: Skeletal changes of organisms transitioning from water to land and Vertebrate land invasion
In Late Devonian vertebrate speciation, descendants of pelagic lobe-finned fish — like Eusthenopteron — exhibited a sequence of adaptations: *Panderichthys, suited to muddy shallows *Tiktaalik with limb-like fins that could take it onto land *Early tetrapods in weed-filled swamps, such as: **Acanthostega, which had feet with eight digits **Ichthyostega with limbs Descendants also included pelagic lobe-finned fish such as coelacanth species.
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Most amphibians today remain semiaquatic, living the first stage of their lives as fish-like tadpoles. Several groups of tetrapods, such as the snakes and cetaceans, have lost some or all of their limbs. In addition, many tetrapods have returned to partially aquatic or fully aquatic lives throughout the history of the group (modern examples of fully aquatic tetrapods include cetaceans and sirenians). The first returns to an aquatic lifestyle may have occurred as early as the Carboniferous Period[3] whereas other returns occurred as recently as the Cenozoic, as in cetaceans, pinnipeds,[4] and several modern amphibians.[5]

The change from a body plan for breathing and navigating in water to a body plan enabling the animal to move on land is one of the most profound evolutionary changes known.[6] It is also one of the best understood, largely thanks to a number of significant transitional fossil finds in the late 20th century combined with improved phylogenetic analysis.[1]

Origin

Evolution of fish
Further information: Evolution of fish

The Devonian period is traditionally known as the "Age of Fish", marking the diversification of numerous extinct and modern major fish groups.[7] Among them were the early bony fishes, who diversified and spread in freshwater and brackish environments at the beginning of the period. The early types resembled their cartilaginous ancestors in many features of their anatomy, including a shark-like tailfin, spiral gut, large pectoral fins stiffened in front by skeletal elements and a largely unossified axial skeleton.[8]

They did, however, have certain traits separating them from cartilaginous fishes, traits that would become pivotal in the evolution of terrestrial forms. With the exception of a pair of spiracles, the gills did not open singly to the exterior as they do in sharks; rather, they were encased in a gill chamber stiffened by membrane bones and covered by a bony operculum, with a single opening to the exterior. The cleithrum bone, forming the posterior margin of the gill chamber, also functioned as anchoring for the pectoral fins. The cartilaginous fishes do not have such an anchoring for the pectoral fins. This allowed for a movable joint at the base of the fins in the early bony fishes, and would later function in a weight bearing structure in tetrapods. As part of the overall armour of rhomboid cosmin scales, the skull had a full cover of dermal bone, constituting a skull roof over the otherwise shark-like cartilaginous inner cranium. Importantly, they also had a pair of ventral paired lungs,[9] a feature lacking in sharks and rays.

It was assumed that fishes to a large degree evolved around reefs, but since their origin about 480 million years ago, they lived in near-shore environments like intertidal areas or permanently shallow lagoons and didn't start to proliferate into other biotopes before 60 million years later. A few adapted to deeper water, while solid and heavily built forms stayed where they were or migrated into freshwater.[10][11] The increase of primary productivity on land during the late Devonian changed the freshwater ecosystems. When nutrients from plants were released into lakes and rivers, they were absorbed by microorganisms which in turn was eaten by invertebrates, which served as food for vertebrates. Some fish also became detritivores.[12] Early tetrapods evolved a tolerance to environments which varied in salinity, such as estuaries or deltas.[13]

Lungs before land

The lung/swim bladder originated as an outgrowth of the gut, forming a gas-filled bladder above the digestive system. In its primitive form, the air bladder was open to the alimentary canal, a condition called physostome and still found in many fish.[14] The primary function is not entirely certain. One consideration is buoyancy. The heavy scale armour of the early bony fishes would certainly weigh the animals down. In cartilaginous fishes, lacking a swim bladder, the open sea sharks need to swim constantly to avoid sinking into the depths, the pectoral fins providing lift.[15] Another factor is oxygen consumption. Ambient oxygen was relatively low in the early Devonian, possibly about half of modern values.[16] Per unit volume, there is much more oxygen in air than in water, and vertebrates are active animals with a high energy requirement compared to invertebrates of similar sizes.[17][18] The Devonian saw increasing oxygen levels which opened up new ecological niches by allowing groups able to exploit the additional oxygen to develop into active, large-bodied animals.[16] Particularly in tropical swampland habitats, atmospheric oxygen is much more stable, and may have prompted a reliance of lungs rather than gills for primary oxygen uptake.[19][20] In the end, both buoyancy and breathing may have been important, and some modern physostome fishes do indeed use their bladders for both.

To function in gas exchange, lungs require a blood supply. In cartilaginous fishes and teleosts, the heart lies low in the body and pumps blood forward through the ventral aorta, which splits up in a series of paired aortic arches, each corresponding to a gill arch.[21] The aortic arches then merge above the gills to form a dorsal aorta supplying the body with oxygenated blood. In lungfishes, bowfin and bichirs, the swim bladder is supplied with blood by paired pulmonary arteries branching off from the hindmost (6th) aortic arch.[22] The same basic pattern is found in the lungfish Protopterus and in terrestrial salamanders, and was probably the pattern found in the tetrapods' immediate ancestors as well as the first tetrapods.[23] In most other bony fishes the swim bladder is supplied with blood by the dorsal aorta.[22]

The breath

In order for the lungs to allow gas exchange, the lungs first need to have gas in them. In modern tetrapods, three important breathing mechanisms are conserved from early ancestors, the first being a CO2/H+ detection system. In modern tetrapod breathing, the impulse to take a breath is triggered by a buildup of CO2 in the bloodstream and not a lack of O2.[24] A similar CO2/H+ detection system is found in all Osteichthyes, which implies that the last common ancestor of all Osteichthyes had a need of this sort of detection system.[24][25] The second mechanism for a breath is a surfactant system in the lungs to facilitate gas exchange. This is also found in all Osteichthyes, even those that are almost entirely aquatic.[26][27] The highly conserved nature of this system suggests that even aquatic Osteichthyes have some need for a surfactant system, which may seem strange as there is no gas underwater. The third mechanism for a breath is the actual motion of the breath. This mechanism predates the last common ancestor of Osteichthyes, as it can be observed in Lampetra camtshatica, the sister clade to Osteichthyes. In Lampreys, this mechanism takes the form of a "cough", where the lamprey shakes its body to allow water flow across its gills. When CO2 levels in the lamprey's blood climb too high, a signal is sent to a central pattern generator that causes the lamprey to "cough" and allow CO2 to leave its body.[28][29] This linkage between the CO2 detection system and the central pattern generator is extremely similar to the linkage between these two systems in tetrapods, which implies homology.

External and internal nares

The nostrils in most bony fish differ from those of tetrapods. Normally, bony fish have four nares (nasal openings), one naris behind the other on each side. As the fish swims, water flows into the forward pair, across the olfactory tissue, and out through the posterior openings. This is true not only of ray-finned fish but also of the coelacanth, a fish included in the Sarcopterygii, the group that also includes the tetrapods. In contrast, the tetrapods have only one pair of nares externally but also sport a pair of internal nares, called choanae, allowing them to draw air through the nose. Lungfish are also sarcopterygians with internal nostrils, but these are sufficiently different from tetrapod choanae that they have long been recognized as an independent development.[30]

The evolution of the tetrapods' internal nares was hotly debated in the 20th century. The internal nares could be one set of the external ones (usually presumed to be the posterior pair) that have migrated into the mouth, or the internal pair could be a newly evolved structure. To make way for a migration, however, the two tooth-bearing bones of the upper jaw, the maxilla and the premaxilla, would have to separate to let the nostril through and then rejoin; until recently, there was no evidence for a transitional stage, with the two bones disconnected. Such evidence is now available: a small lobe-finned fish called Kenichthys, found in China and dated at around 395 million years old, represents evolution "caught in mid-act", with the maxilla and premaxilla separated and an aperture—the incipient choana—on the lip in between the two bones.[31] Kenichthys is more closely related to tetrapods than is the coelacanth,[32] which has only external nares; it thus represents an intermediate stage in the evolution of the tetrapod condition. The reason for the evolutionary movement of the posterior nostril from the nose to lip, however, is not well understood.

Into the shallows
Devonian fishes, including an early shark Cladoselache, Eusthenopteron and other lobe-finned fishes, and the placoderm Bothriolepis (Joseph Smit, 1905).

The relatives of Kenichthys soon established themselves in the waterways and brackish estuaries and became the most numerous of the bony fishes throughout the Devonian and most of the Carboniferous. The basic anatomy of group is well known thanks to the very detailed work on Eusthenopteron by Erik Jarvik in the second half of the 20th century.[33] The bones of the skull roof were broadly similar to those of early tetrapods and the teeth had an infolding of the enamel similar to that of labyrinthodonts. The paired fins had a build with bones distinctly homologous to the humerus, ulna, and radius in the fore-fins and to the femur, tibia, and fibula in the pelvic fins.[34]

There were a number of families: Rhizodontida, Canowindridae, Elpistostegidae, Megalichthyidae, Osteolepidae and Tristichopteridae.[35] Most were open-water fishes, and some grew to very large sizes; adult specimens are several meters in length.[36] The Rhizodontid Rhizodus is estimated to have grown to 7 meters (23 feet), making it the largest freshwater fish known.[37]

While most of these were open-water fishes, one group, the Elpistostegalians, adapted to life in the shallows. They evolved flat bodies for movement in very shallow water, and the pectoral and pelvic fins took over as the main propulsion organs. Most median fins disappeared, leaving only a protocercal tailfin. Since the shallows were subject to occasional oxygen deficiency, the ability to breathe atmospheric air with the swim bladder became increasingly important.[6] The spiracle became large and prominent, enabling these fishes to draw air.

Skull morphology

The tetrapods have their root in the early Devonian tetrapodomorph fish.[38] Primitive tetrapods developed from an osteolepid tetrapodomorph lobe-finned fish (sarcopterygian-crossopterygian), with a two-lobed brain in a flattened skull. The coelacanth group represents marine sarcopterygians that never acquired these shallow-water adaptations. The sarcopterygians apparently took two different lines of descent and are accordingly separated into two major groups: the Actinistia (including the coelacanths) and the Rhipidistia (which include extinct lines of lobe-finned fishes that evolved into the lungfish and the tetrapodomorphs).

From fins to feet
Stalked fins like those of the bichirs can be used for terrestrial movement

The oldest known tetrapodomorph is Kenichthys from China, dated at around 395 million years old. Two of the earliest tetrapodomorphs, dating from 380 Ma, were Gogonasus and Panderichthys.[39] They had choanae and used their fins to move through tidal channels and shallow waters choked with dead branches and rotting plants.[40] Their fins could have been used to attach themselves to plants or similar while they were lying in ambush for prey. The universal tetrapod characteristics of front limbs that bend forward from the elbow and hind limbs that bend backward from the knee can plausibly be traced to early tetrapods living in shallow water. Pelvic bone fossils from Tiktaalik shows, if representative for early tetrapods in general, that hind appendages and pelvic-propelled locomotion originated in water before terrestrial adaptations.[41]

Another indication that feet and other tetrapod traits evolved while the animals were still aquatic is how they were feeding. They did not have the modifications of the skull and jaw that allowed them to swallow prey on land. Prey could be caught in the shallows, at the water's edge or on land, but had to be eaten in water where hydrodynamic forces from the expansion of their buccal cavity would force the food into their esophagus.[42]

It has been suggested that the evolution of the tetrapod limb from fins in lobe-finned fishes is related to expression of the HOXD13 gene or the loss of the proteins actinodin 1 and actinodin 2, which are involved in fish fin development.[43][44] Robot simulations suggest that the necessary nervous circuitry for walking evolved from the nerves governing swimming, utilizing the sideways oscillation of the body with the limbs primarily functioning as anchoring points and providing limited thrust.[45] This type of movement, as well as changes to the pectoral girdle are similar to those seen in the fossil record can be induced in bichirs by raising them out of water.[46]

A 2012 study using 3D reconstructions of Ichthyostega concluded that it was incapable of typical quadrupedal gaits. The limbs could not move alternately as they lacked the necessary rotary motion range. In addition, the hind limbs lacked the necessary pelvic musculature for hindlimb-driven land movement. Their most likely method of terrestrial locomotion is that of synchronous "crutching motions", similar to modern mudskippers.[47] (Viewing several videos of mudskipper "walking" shows that they move by pulling themselves forward with both pectoral fins at the same time (left & right pectoral fins move simultaneously, not alternatively). The fins are brought forward and planted; the shoulders then rotate rearward, advancing the body & dragging the tail as a third point of contact. There are no rear "limbs"/fins, and there is no significant flexure of the spine involved.)

Denizens of the swamp

The first tetrapods probably evolved in coastal and brackish marine environments, and in shallow and swampy freshwater habitats.[48] Formerly, researchers thought the timing was towards the end of the Devonian. In 2010, this belief was challenged by the discovery of the oldest known tetrapod tracks, preserved in marine sediments of the southern coast of Laurasia, now Świętokrzyskie (Holy Cross) Mountains of Poland. They were made during the Eifelian stage at the end of the Middle Devonian. The tracks, some of which show digits, date to about 395 million years ago—18 million years earlier than the oldest known tetrapod body fossils.[49] Additionally, the tracks show that the animal was capable of thrusting its arms and legs forward, a type of motion that would have been impossible in tetrapodomorph fish like Tiktaalik. The animal that produced the tracks is estimated to have been up to 2.5 metres (8.2 ft) long with footpads up to 26 centimetres (10 in) wide, although most tracks are only 15 centimetres (5.9 in) wide.[50]

The new finds suggest that the first tetrapods may have lived as opportunists on the tidal flats, feeding on marine animals that were washed up or stranded by the tide.[49] Currently, however, fish are stranded in significant numbers only at certain times of year, as in alewife spawning season; such strandings could not provide a significant supply of food for predators. There is no reason to suppose that Devonian fish were less prudent than those of today.[51] According to Melina Hale of University of Chicago, not all ancient trackways are necessarily made by early tetrapods, but could also be created by relatives of the tetrapods who used their fleshy appendages in a similar substrate-based locomotion.[52][53]

Palaeozoic tetrapods

Devonian tetrapods

Research by Jennifer A. Clack and her colleagues showed that the very earliest tetrapods, animals similar to Acanthostega, were wholly aquatic and quite unsuited to life on land. This is in contrast to the earlier view that fish had first invaded the land — either in search of prey (like modern mudskippers) or to find water when the pond they lived in dried out — and later evolved legs, lungs, etc.

By the late Devonian, land plants had stabilized freshwater habitats, allowing the first wetland ecosystems to develop, with increasingly complex food webs that afforded new opportunities. Freshwater habitats were not the only places to find water filled with organic matter and dense vegetation near the water's edge. Swampy habitats like shallow wetlands, coastal lagoons and large brackish river deltas also existed at this time, and there is much to suggest that this is the kind of environment in which the tetrapods evolved. Early fossil tetrapods have been found in marine sediments, and because fossils of primitive tetrapods in general are found scattered all around the world, they must have spread by following the coastal lines — they could not have lived in freshwater only.

One analysis from the University of Oregon suggests no evidence for the "shrinking waterhole" theory - transitional fossils are not associated with evidence of shrinking puddles or ponds - and indicates that such animals would probably not have survived short treks between depleted waterholes.[54] The new theory suggests instead that proto-lungs and proto-limbs were useful adaptations to negotiate the environment in humid, wooded floodplains.[55]

The Devonian tetrapods went through two major bottlenecks during what is known as the Late Devonian extinction; one at the end of the Frasnian stage, and one twice as large at the end of the following Famennian stage. These events of extinctions led to the disappearance of primitive tetrapods with fish-like features like Ichthyostega and their primary more aquatic relatives.[56] When tetrapods reappear in the fossil record after the Devonian extinctions, the adult forms are all fully adapted to a terrestrial existence, with later species secondary adapted to an aquatic lifestyle.[57]

Excretion in tetrapods

The common ancestor of all present gnathostomes (jawed-vertebrates) lived in freshwater, and later migrated back to the sea. To deal with the much higher salinity in sea water, they evolved the ability to turn the nitrogen waste product ammonia into harmless urea, storing it in the body to give the blood the same osmolarity as the sea water without poisoning the organism. This is the system currently found in cartilaginous fishes. Ray-finned fishes (Actinopterygii) later returned to freshwater and lost this ability, while the fleshy-finned fishes (Sarcopterygii) retained it. Since the blood of ray-finned fishes contains more salt than freshwater, they could simply get rid of ammonia through their gills. When they finally returned to the sea again, they did not recover their old trick of turning ammonia to urea, and they had to evolve salt excreting glands instead. Lungfishes do the same when they are living in water, making ammonia and no urea, but when the water dries up and they are forced to burrow down in the mud, they switch to urea production. Like cartilaginous fishes, the coelacanth can store urea in its blood, as can the only known amphibians that can live for long periods of time in salt water (the toad Bufo marinus and the frog Rana cancrivora). These are traits they have inherited from their ancestors.

If early tetrapods lived in freshwater, and if they lost the ability to produce urea and used ammonia only, they would have to evolve it from scratch again later. Not a single species of all the ray-finned fishes living today has been able to do that, so it is not likely the tetrapods would have done so either. Terrestrial animals that can only produce ammonia would have to drink constantly, making a life on land impossible (a few exceptions exist, as some terrestrial woodlice can excrete their nitrogenous waste as ammonia gas). This probably also was a problem at the start when the tetrapods started to spend time out of water, but eventually the urea system would dominate completely. Because of this it is not likely they emerged in freshwater (unless they first migrated into freshwater habitats and then migrated onto land so shortly after that they still retained the ability to make urea), although some species never left, or returned to, the water could of course have adapted to freshwater lakes and rivers.

Lungs

It is now clear that the common ancestor of the bony fishes (Osteichthyes) had a primitive air-breathing lung—later evolved into a swim bladder in most actinopterygians (ray-finned fishes). This suggests that crossopterygians evolved in warm shallow waters, using their simple lung when the oxygen level in the water became too low.

Fleshy lobe-fins supported on bones rather than ray-stiffened fins seem to have been an ancestral trait of all bony fishes (Osteichthyes). The lobe-finned ancestors of the tetrapods evolved them further, while the ancestors of the ray-finned fishes (Actinopterygii) evolved their fins in a different direction. The most primitive group of actinopterygians, the bichirs, still have fleshy frontal fins.

Fossils of early tetrapods

Nine genera of Devonian tetrapods have been described, several known mainly or entirely from lower jaw material. All but one were from the Laurasian supercontinent, which comprised Europe, North America and Greenland. The only exception is a single Gondwanan genus, Metaxygnathus, which has been found in Australia.

The first Devonian tetrapod identified from Asia was recognized from a fossil jawbone reported in 2002. The Chinese tetrapod Sinostega pani was discovered among fossilized tropical plants and lobe-finned fish in the red sandstone sediments of the Ningxia Hui Autonomous Region of northwest China. This finding substantially extended the geographical range of these animals and has raised new questions about the worldwide distribution and great taxonomic diversity they achieved within a relatively short time.

Oldest tetrapod tracks from Zachelmie in relation to key Devonian tetrapodomorph body fossils
Eusthenopteron
Panderichthys
Tiktaalik
Acanthostega
Ichthyostega
Hynerpeton
Tulerpeton
Crassigyrinus
Diadectes

These earliest tetrapods were not terrestrial. The earliest confirmed terrestrial forms are known from the early Carboniferous deposits, some 20 million years later. Still, they may have spent very brief periods out of water and would have used their legs to paw their way through the mud.

Why they went to land in the first place is still debated. One reason could be that the small juveniles who had completed their metamorphosis had what it took to make use of what land had to offer. Already adapted to breathe air and move around in shallow waters near land as a protection (just as modern fish and amphibians often spend the first part of their life in the comparative safety of shallow waters like mangrove forests), two very different niches partially overlapped each other, with the young juveniles in the diffuse line between. One of them was overcrowded and dangerous while the other was much safer and much less crowded, offering less competition over resources. The terrestrial niche was also a much more challenging place for primarily aquatic animals, but because of the way evolution and selection pressure work, those juveniles who could take advantage of this would be rewarded. Once they gained a small foothold on land, thanks to their pre-adaptations, favourable variations in their descendants would gradually result in continuing evolution and diversification.

At this time the abundance of invertebrates crawling around on land and near water, in moist soil and wet litter, offered a food supply. Some were even big enough to eat small tetrapods, but the land was free from dangers common in the water.

From water to land
Main article: Vertebrate land invasion

Initially making only tentative forays onto land, tetrapods adapted to terrestrial environments over time and spent longer periods away from the water. It is also possible that the adults started to spend some time on land (as the skeletal modifications in early tetrapods such as Ichthyostega suggests) to bask in the sun close to the water's edge, while otherwise being mostly aquatic.

Carboniferous tetrapods

Until the 1990s, there was a 30 million year gap in the fossil record between the late Devonian tetrapods and the reappearance of tetrapod fossils in recognizable mid-Carboniferous amphibian lineages. It was referred to as "Romer's Gap", which now covers the period from about 360 to 345 million years ago (the Devonian-Carboniferous transition and the early Mississippian), after the palaeontologist who recognized it.

During the "gap", tetrapod backbones developed, as did limbs with digits and other adaptations for terrestrial life. Ears, skulls and vertebral columns all underwent changes too. The number of digits on hands and feet became standardized at five, as lineages with more digits died out. Thus, those very few tetrapod fossils found in this "gap" are all the more prized by palaeontologists because they document these significant changes and clarify their history.

The transition from an aquatic, lobe-finned fish to an air-breathing amphibian was a significant and fundamental one in the evolutionary history of the vertebrates. For an organism to live in a gravity-neutral aqueous environment, then colonize one that requires an organism to support its entire weight and possess a mechanism to mitigate dehydration, required significant adaptations or exaptations within the overall body plan, both in form and in function. Eryops, an example of an animal that made such adaptations, refined many of the traits found in its fish ancestors. Sturdy limbs supported and transported its body while out of water. A thicker, stronger backbone prevented its body from sagging under its own weight. Also, through the reshaping of vestigial fish jaw bones, a rudimentary middle ear began developing to connect to the piscine inner ear, allowing Eryops to amplify, and so better sense, airborne sound.

By the Visean (mid-Carboniferous) stage, the early tetrapods had radiated into at least three or four main branches. Some of these different branches represent the ancestors to all living tetrapods. This means that the common ancestor of all living tetrapods likely lived in the Carboniferous. Under a narrow cladistic definition of Tetrapoda (also known as crown-Tetrapoda), which only includes descendants of this common ancestor, tetrapods first appeared in the Carboniferous. Recognizable early tetrapods (in the broad sense) are representative of the temnospondyls (e.g. Eryops) lepospondyls (e.g. Diplocaulus), anthracosaurs, which were the relatives and ancestors of the Amniota, and possibly the baphetids, which are thought to be related to temnospondyls and whose status as a main branch is yet unresolved. Depending on which authorities one follows, modern amphibians (frogs, salamanders and caecilians) are most probably derived from either temnospondyls or lepospondyls (or possibly both, although this is now a minority position).

The first amniotes (clade of vertebrates that today includes reptiles, mammals, and birds) are known from the early part of the Late Carboniferous. By the Triassic, this group had already radiated into the earliest mammals, turtles, and crocodiles (lizards and birds appeared in the Jurassic, and snakes in the Cretaceous). This contrasts sharply with the (possibly fourth) Carboniferous group, the baphetids, which have left no extant surviving lineages.

Carboniferous rainforest collapse

Amphibians and reptiles were strongly affected by the Carboniferous rainforest collapse (CRC), an extinction event that occurred ~307 million years ago. The Carboniferous period has long been associated with thick, steamy swamps and humid rainforests.[58] Since plants form the base of almost all of Earth's ecosystems, any changes in plant distribution have always affected animal life to some degree. The sudden collapse of the vital rainforest ecosystem profoundly affected the diversity and abundance of the major tetrapod groups that relied on it.[59] The CRC, which was a part of one of the top two most devastating plant extinctions in Earth's history, was a self-reinforcing and very rapid change of environment wherein the worldwide climate became much drier and cooler overall (although much new work is being done to better understand the fine-grained historical climate changes in the Carboniferous-Permian transition and how they arose[60]).

The ensuing worldwide plant reduction resulting from the difficulties plants encountered in adjusting to the new climate caused a progressive fragmentation and collapse of rainforest ecosystems. This reinforced and so further accelerated the collapse by sharply reducing the amount of animal life which could be supported by the shrinking ecosystems at that time. The outcome of this animal reduction was a crash in global carbon dioxide levels, which impacted the plants even more.[61] The aridity and temperature drop which resulted from this runaway plant reduction and decrease in a primary greenhouse gas caused the Earth to rapidly enter a series of intense Ice Ages.[58]

This impacted amphibians in particular in a number of ways. The enormous drop in sea level due to greater quantities of the world's water being locked into glaciers profoundly affected the distribution and size of the semiaquatic ecosystems which amphibians favored, and the significant cooling of the climate further narrowed the amount of new territory favorable to amphibians. Given that among the hallmarks of amphibians are an obligatory return to a body of water to lay eggs, a delicate skin prone to desiccation (thereby often requiring the amphibian to be relatively close to water throughout its life), and a reputation of being a bellwether species for disrupted ecosystems due to the resulting low resilience to ecological change,[62] amphibians were particularly devastated, with the Labyrinthodonts among the groups faring worst. In contrast, reptiles - whose amniotic eggs have a membrane that enables gas exchange out of water, and which thereby can be laid on land - were better adapted to the new conditions. Reptiles invaded new niches at a faster rate and began diversifying their diets, becoming herbivorous and carnivorous, rather than feeding exclusively on insects and fish.[63] Meanwhile, the severely impacted amphibians simply could not out-compete reptiles in mastering the new ecological niches,[64] and so were obligated to pass the tetrapod evolutionary torch to the increasingly successful and swiftly radiating reptiles.

Permian tetrapods

In the Permian period: early "amphibia" (labyrinthodonts) clades included temnospondyl and anthracosaur; while amniote clades included the Sauropsida and the Synapsida. Sauropsida would eventually evolve into today's reptiles and birds; whereas Synapsida would evolve into today's mammals. During the Permian, however, the distinction was less clear—amniote fauna being typically described as either reptile or as mammal-like reptile. The latter (synapsida) were the most important and successful Permian animals.

The end of the Permian saw a major turnover in fauna during the Permian–Triassic extinction event: probably the most severe mass extinction event of the phanerozoic. There was a protracted loss of species, due to multiple extinction pulses.[65] Many of the once large and diverse groups died out or were greatly reduced.

Mesozoic tetrapods

Life on Earth seemed to recover quickly after the Permian extinctions, though this was mostly in the form of disaster taxa such as the hardy Lystrosaurus. Specialized animals that formed complex ecosystems with high biodiversity, complex food webs, and a variety of niches, took much longer to recover.[65] Current research indicates that this long recovery was due to successive waves of extinction, which inhibited recovery, and to prolonged environmental stress to organisms that continued into the Early Triassic. Recent research indicates that recovery did not begin until the start of the mid-Triassic, 4M to 6M years after the extinction;[66] and some writers estimate that the recovery was not complete until 30M years after the P-Tr extinction, i.e. in the late Triassic.[65]

A small group of reptiles, the diapsids, began to diversify during the Triassic, notably the dinosaurs. By the late Mesozoic, the large labyrinthodont groups that first appeared during the Paleozoic such as temnospondyls and reptile-like amphibians had gone extinct. All current major groups of sauropsids evolved during the Mesozoic, with birds first appearing in the Jurassic as a derived clade of theropod dinosaurs. Many groups of synapsids such as anomodonts and therocephalians that once comprised the dominant terrestrial fauna of the Permian also became extinct during the Mesozoic; during the Triassic, however, one group (Cynodontia) gave rise to the descendant taxon Mammalia, which survived through the Mesozoic to later diversify during the Cenozoic.

Cenozoic tetrapods

The Cenozoic era began with the end of the Mesozoic era and the Cretaceous epoch; and continues to this day. The beginning of the Cenozoic was marked by the Cretaceous-Paleogene extinction event during which all non-avian dinosaurs became extinct. The Cenozoic is sometimes called the "Age of Mammals".

During the Mesozoic, the prototypical mammal was a small nocturnal insectivore something like a tree shrew. Due to their nocturnal habits, most mammals lost their color vision, and greatly improved their sense of hearing. All mammals of today are shaped by this origin. Primates later re-evolved color-vision.

During the Paleocene and Eocene, most mammals remained small (under 20 kg). Cooling climate in the Oligocene and Miocene, and the expansion of grasslands favored the evolution of larger mammalian species.

Ratites run, and penguins swim and waddle: but the majority of birds are rather small, and can fly. Some birds use their ability to fly to complete epic globe-crossing migrations, while others such as frigate birds fly over the oceans for months on end.

Bats have also taken flight, and along with cetaceans have developed echolocation or sonar.

Whales, seals, manatees, and sea otters have returned to the ocean and an aquatic lifestyle.

Vast herds of ruminant ungulates populate the grasslands and forests. Carnivores have evolved to keep the herd-animal populations in check.

Extant (living) tetrapods

Following the great faunal turnover at the end of the Mesozoic, only six major groups of tetrapods were left, all of which also include many extinct groups:

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gollark: I don't know why it said `env` at the end, but that was quite a good explanation.
gollark: It really seems like this should just be called `apply`, though.
gollark: I don't care, Codex explained it.
gollark: <@356107472269869058> Explain || I will ask Codex what it does.

References
  1. Shubin, N. (2008). Your Inner Fish: A Journey Into the 3.5-Billion-Year History of the Human Body. New York: Pantheon Books. ISBN 978-0-375-42447-2.
  2. Clack, Jennifer A. (1997). "Devonian tetrapod trackways and trackmakers; a review of the fossils and footprints". Palaeogeography, Palaeoclimatology, Palaeoecology. 130 (1–4): 227–250. Bibcode:1997PPP...130..227C. doi:10.1016/S0031-0182(96)00142-3.CS1 maint: ref=harv (link)
  3. Laurin, M. (2010). How Vertebrates Left the Water. Berkeley, California, USA.: University of California Press. ISBN 978-0-520-26647-6.
  4. Canoville, Aurore; Laurin, Michel (2010). "Evolution of humeral microanatomy and lifestyle in amniotes, and some comments on paleobiological inferences". Biological Journal of the Linnean Society. 100 (2): 384–406. doi:10.1111/j.1095-8312.2010.01431.x.CS1 maint: ref=harv (link)
  5. Laurin, Michel; Canoville, Aurore; Quilhac, Alexandra (2009). "Use of paleontological and molecular data in supertrees for comparative studies: the example of lissamphibian femoral microanatomy". Journal of Anatomy. 215 (2): 110–123. doi:10.1111/j.1469-7580.2009.01104.x. PMC 2740958. PMID 19508493.CS1 maint: ref=harv (link)
  6. Long JA, Gordon MS (2004). "The greatest step in vertebrate history: a paleobiological review of the fish-tetrapod transition". Physiol. Biochem. Zool. 77 (5): 700–19. doi:10.1086/425183. PMID 15547790. Archived from the original on 2016-04-12. Retrieved 2014-03-09.CS1 maint: ref=harv (link) as PDF Archived 2013-10-29 at the Wayback Machine
  7. Wells, H. G. (1922). "Chapter IV: The Age of Fishes". A Short History of the World. Macmillan. ISBN 978-1-58734-075-8. Archived from the original on 2014-02-01. Retrieved 2014-03-09.CS1 maint: ref=harv (link).
  8. Colbert, Edwin H. (1969). Evolution of the Vertebrates (2nd ed.). John Wiley & Sons. pp. 49–53.
  9. Benton 2005, p. 67
  10. "Vertebrate evolution kicked off in lagoons".
  11. The nearshore cradle of early vertebrate diversification | Science
  12. The Terrestrialization Process: Modelling Complex Interactions at the Biosphere-geosphere Interface
  13. Euryhaline ecology of early tetrapods revealed by stable isotopes - Nature
  14. Steen, Johan B. (1970). "The Swim Bladder as a Hydrostatic Organ". Fish Physiology. 4. San Diego, California: Academic Press, Inc. pp. 413–443.
  15. Videler, J.J. (1993). Fish Swimming. New York: Chapman & Hall.
  16. Dahl TW, Hammarlund EU, Anbar AD, et al. (October 2010). "Devonian rise in atmospheric oxygen correlated to the radiations of terrestrial plants and large predatory fish". Proc. Natl. Acad. Sci. U.S.A. 107 (42): 17911–5. Bibcode:2010PNAS..10717911D. doi:10.1073/pnas.1011287107. PMC 2964239. PMID 20884852.CS1 maint: ref=harv (link)
  17. Vaquer-Sunyer R, Duarte CM (October 2008). "Thresholds of hypoxia for marine biodiversity". Proc. Natl. Acad. Sci. U.S.A. 105 (40): 15452–7. Bibcode:2008PNAS..10515452V. doi:10.1073/pnas.0803833105. PMC 2556360. PMID 18824689.CS1 maint: ref=harv (link)
  18. Gray, J.; Wu, R.; Or, Y. (2002). Effects of hypoxia and organic enrichment on the coastal marine environment. Marine Ecology Progress Series. 238. pp. 249–279. Bibcode:2002MEPS..238..249G. doi:10.3354/meps238249.
  19. Armbruster, Jonathan W. (1998). "Modifications of the Digestive Tract for Holding Air in Loricariid and Scoloplacid Catfishes" (PDF). Copeia. 1998 (3): 663–675. doi:10.2307/1447796. JSTOR 1447796. Archived (PDF) from the original on 2009-03-26. Retrieved 25 June 2009.CS1 maint: ref=harv (link)
  20. Long, J.A. (1990). "Heterochrony and the origin of tetrapods". Lethaia. 23 (2): 157–166. doi:10.1111/j.1502-3931.1990.tb01357.x.CS1 maint: ref=harv (link)
  21. Romer, A.S. (1949). The Vertebrate Body. Philadelphia: W.B. Saunders. (2nd ed. 1955; 3rd ed. 1962; 4th ed. 1970)
  22. Kent, G.C.; Miller, L. (1997). Comparative anatomy of the vertebrates (8th ed.). Dubuque: Wm. C. Brown Publishers. ISBN 978-0-697-24378-2.
  23. Hildebran, M.; Goslow, G. (2001). Analysis of Vertebrate Structure (5th ed.). New York: John Wiley. ISBN 978-0-471-29505-1.
  24. Fernandes, Marisa Narciso; da Cruz, André Luis; da Costa, Oscar Tadeu Ferreira; Perry, Steven Franklin (September 2012). "Morphometric partitioning of the respiratory surface area and diffusion capacity of the gills and swim bladder in juvenile Amazonian air-breathing fish, Arapaima gigas". Micron (Oxford, England: 1993). 43 (9): 961–970. doi:10.1016/j.micron.2012.03.018. ISSN 1878-4291. PMID 22512942.
  25. Brauner, C. J.; Matey, V.; Wilson, J. M.; Bernier, N. J.; Val, A. L. (2004-04-01). "Transition in organ function during the evolution of air-breathing; insights from Arapaima gigas, an obligate air-breathing teleost from the Amazon". Journal of Experimental Biology. 207 (9): 1433–1438. doi:10.1242/jeb.00887. ISSN 0022-0949. PMID 15037637.
  26. Daniels, Christopher B.; Orgeig, Sandra; Sullivan, Lucy C.; Ling, Nicholas; Bennett, Michael B.; Schürch, Samuel; Val, Adalberto Luis; Brauner, Colin J. (September 2004). "The origin and evolution of the surfactant system in fish: insights into the evolution of lungs and swim bladders". Physiological and Biochemical Zoology. 77 (5): 732–749. CiteSeerX 10.1.1.385.9019. doi:10.1086/422058. ISSN 1522-2152. PMID 15547792.
  27. Orgeig, Sandra; Morrison, Janna L.; Daniels, Christopher B. (2011-08-31). "Prenatal development of the pulmonary surfactant system and the influence of hypoxia". Respiratory Physiology & Neurobiology. 178 (1): 129–145. doi:10.1016/j.resp.2011.05.015. ISSN 1878-1519. PMID 21642020.
  28. Hsia, Connie C. W.; Schmitz, Anke; Lambertz, Markus; Perry, Steven F.; Maina, John N. (April 2013). "Evolution of Air Breathing: Oxygen Homeostasis and the Transitions from Water to Land and Sky". Comprehensive Physiology. 3 (2): 849–915. doi:10.1002/cphy.c120003. ISSN 2040-4603. PMC 3926130. PMID 23720333.
  29. Hoffman, M.; Taylor, B. E.; Harris, M. B. (April 2016). "Evolution of lung breathing from a lungless primitive vertebrate". Respiratory Physiology & Neurobiology. 224: 11–16. doi:10.1016/j.resp.2015.09.016. ISSN 1878-1519. PMC 5138057. PMID 26476056.
  30. Panchen, A. L. (1967). "The nostrils of choanate fishes and early tetrapods". Biol. Rev. 42 (3): 374–419. doi:10.1111/j.1469-185X.1967.tb01478.x. PMID 4864366.CS1 maint: ref=harv (link)
  31. Zhu, Min; Ahlberg, Per E. (2004). "The origin of the internal nostril of tetrapods". Nature. 432 (7013): 94–7. Bibcode:2004Natur.432...94Z. doi:10.1038/nature02843. PMID 15525987. Lay summary – innovations-report (November 4, 2004).CS1 maint: ref=harv (link)
  32. Coates, Michael I.; Jeffery, Jonathan E.; Ruta, Marcella (2002). "Fins to limbs: what the fossils say" (PDF). Evolution and Development. 4 (5): 390–401. doi:10.1046/j.1525-142X.2002.02026.x. PMID 12356269. Archived (PDF) from the original on 2010-06-10. Retrieved February 18, 2013.CS1 maint: ref=harv (link)
  33. Geological Survey of Canada (2008-02-07). "Past lives: Chronicles of Canadian Paleontology: Eusthenopteron - the Prince of Miguasha". Archived from the original on 2004-12-11. Retrieved 2009-02-10.
  34. Meunier, François J.; Laurin, Michel (January 2012). "A microanatomical and histological study of the fin long bones of the Devonian sarcopterygian Eusthenopteron foordi". Acta Zoologica. 93 (1): 88–97. doi:10.1111/j.1463-6395.2010.00489.x.CS1 maint: ref=harv (link)
  35. Ahlberg, P. E.; Johanson, Z. (1998). "Osteolepiforms and the ancestry of tetrapods" (PDF). Nature. 395 (6704): 792–794. Bibcode:1998Natur.395..792A. doi:10.1038/27421. Archived from the original (PDF) on 2014-11-24. Retrieved 2014-03-09.CS1 maint: ref=harv (link)
  36. Moy-Thomas, J. A. (1971). Palaeozoic fishes (2d ed., extensively rev. ed.). Philadelphia: Saunders. ISBN 978-0-7216-6573-3.
  37. Andrews, S. M. (January 1985). "Rhizodont crossopterygian fish from the Dinantian of Foulden, Berwickshire, Scotland, with a re-evaluation of this group". Transactions of the Royal Society of Edinburgh: Earth Sciences. 76 (1): 67–95. doi:10.1017/S0263593300010324.CS1 maint: ref=harv (link)
  38. Ruta, Marcello; Jeffery, Jonathan E.; Coates, Michael I. (2003). "A supertree of early tetrapods". Proceedings of the Royal Society B. 270 (1532): 2507–16. doi:10.1098/rspb.2003.2524. PMC 1691537. PMID 14667343.CS1 maint: ref=harv (link)
  39. Monash University. "West Australian Fossil Find Rewrites Land Mammal Evolution Archived 2017-08-21 at the Wayback Machine." ScienceDaily 19 October 2006. Accessed 11 March 2009
  40. "Tetrapoda". Palaeos website. Archived from the original on 2013-03-29. Retrieved 11 October 2012. Even closer related was Panderichthys, who even had a choana. These fishes used their fins as paddles in shallow-water habitats choked with plants and detritus.
  41. "375 million-year-old Fish Fossil Sheds Light on Evolution From Fins to Limbs". 2014-01-14. Archived from the original on 2014-04-07. Retrieved 2014-05-31.
  42. Ashley-Ross, M. A.; Hsieh, S. T.; Gibb, A. C.; Blob, R. W. (2013). "Vertebrate Land Invasions—Past, Present, and Future: An Introduction to the Symposium". Integrative and Comparative Biology. 53 (2): 192–196. doi:10.1093/icb/ict048. PMID 23660589. Archived from the original on 2014-10-13. Retrieved 2014-05-31.
  43. Schneider, Igor; Shubin, Neil H. (December 2012). "Making Limbs from Fins". Developmental Cell. 23 (6): 1121–1122. doi:10.1016/j.devcel.2012.11.011. PMID 23237946.
  44. Zhang, J.; Wagh, P.; Guay, D.; Sanchez-Pulido, L.; Padhi, B. K.; Korzh, V.; Andrade-Navarro, M. A.; Akimenko, M. A. (2010). "Loss of fish actinotrichia proteins and the fin-to-limb transition". Nature. 466 (7303): 234–237. Bibcode:2010Natur.466..234Z. doi:10.1038/nature09137. PMID 20574421.
  45. Ijspeert, A. J.; Crespi, A.; Ryczko, D.; Cabelguen, J.-M. (9 March 2007). "From Swimming to Walking with a Salamander Robot Driven by a Spinal Cord Model". Science. 315 (5817): 1416–1420. Bibcode:2007Sci...315.1416I. doi:10.1126/science.1138353. PMID 17347441.CS1 maint: ref=harv (link)
  46. Standen, Emily M.; Du, Trina Y.; Larsson, Hans C. E. (27 August 2014). "Developmental plasticity and the origin of tetrapods". Nature. 513 (7516): 54–58. Bibcode:2014Natur.513...54S. doi:10.1038/nature13708. PMID 25162530.
  47. Stephanie E. Pierce; Jennifer A. Clack; John R. Hutchinson (2012). "Three-dimensional limb joint mobility in the early tetrapod Ichthyostega". Nature. 486 (7404): 524–527. Bibcode:2012Natur.486..523P. doi:10.1038/nature11124. PMID 22722854.CS1 maint: ref=harv (link)
  48. Clack 2002, pp. 86–7
  49. Grzegorz Niedźwiedzki; Piotr Szrek; Katarzyna Narkiewicz; Marek Narkiewicz; Per E. Ahlberg (2010). "Tetrapod trackways from the early Middle Devonian period of Poland". Nature. 463 (7277): 43–8. Bibcode:2010Natur.463...43N. doi:10.1038/nature08623. PMID 20054388.CS1 maint: ref=harv (link)
  50. Rex Dalton (January 6, 2010). "Discovery pushes back date of first four-legged animal". Nature News. Archived from the original on 2010-01-14. Retrieved January 8, 2010.
  51. Clack 2012, p. 140
  52. "A Small Step for Lungfish, a Big Step for the Evolution of Walking". Archived from the original on 2017-07-03. Retrieved 2018-02-28.
  53. King, H. M.; Shubin, N. H.; Coates, M. I.; Hale, M. E. (2011). "Behavioral evidence for the evolution of walking and bounding before terrestriality in sarcopterygian fishes". Proceedings of the National Academy of Sciences. 108 (52): 21146–21151. Bibcode:2011PNAS..10821146K. doi:10.1073/pnas.1118669109. PMC 3248479. PMID 22160688. Archived from the original on 2014-05-30. Retrieved 2014-03-09.
  54. Retallack, Gregory (May 2011). "Woodland Hypothesis for Devonian Tetrapod Evolution" (PDF). Journal of Geology. University of Chicago Press. 119 (3): 235–258. Bibcode:2011JG....119..235R. doi:10.1086/659144. Archived (PDF) from the original on 2013-05-17. Retrieved January 1, 2012.CS1 maint: ref=harv (link)
  55. "A New Theory Emerges for Where Some Fish Became 4-limbed Creatures". ScienceNewsline. December 28, 2011. Archived from the original on 2016-03-04. Retrieved January 17, 2013.
  56. When the Invasion of Land Failed: The Legacy of the Devonian Extinctions
  57. "Research project: The Mid-Palaeozoic biotic crisis: Setting the trajectory of Tetrapod evolution". Archived from the original on 2013-12-12. Retrieved 2014-05-31.
  58. Dimichele, William A.; Cecil, C. Blaine; Montañez, Isabel P.; Falcon-Lang, Howard J. (2010). "Cyclic changes in Pennsylvanian paleoclimate and effects on floristic dynamics in tropical Pangaea". International Journal of Coal Geology. 83 (2–3): 329–344. doi:10.1016/j.coal.2010.01.007.
  59. Davies, Neil S.; Gibling, Martin R. (2013). "The sedimentary record of Carboniferous rivers: Continuing influence of land plant evolution on alluvial processes and Palaeozoic ecosystems". Earth-Science Reviews. 120: 40–79. Bibcode:2013ESRv..120...40D. doi:10.1016/j.earscirev.2013.02.004.
  60. Tabor, Neil J.; Poulsen, Christopher J. (2008). "Palaeoclimate across the Late Pennsylvanian–Early Permian tropical palaeolatitudes: A review of climate indicators, their distribution, and relation to palaeophysiographic climate factors". Palaeogeography, Palaeoclimatology, Palaeoecology. 268 (3–4): 293–310. Bibcode:2008PPP...268..293T. doi:10.1016/j.palaeo.2008.03.052.
  61. Gibling, M.R.; Davies, N.S.; Falcon-Lang, H.J.; Bashforth, A.R.; Dimichele, W.A.; Rygel, M.C.; Ielpi, A. (2014). "Palaeozoic co-evolution of rivers and vegetation: a synthesis of current knowledge". Proceedings of the Geologists' Association. 125 (5–6): 524–533. doi:10.1016/j.pgeola.2013.12.003.
  62. Purves, William K.; Orians, Gordon H.; Heller, H. Craig (1995). Life, The Science of Biology (4th ed.). Sunderland, MA, USA: Sinauer Associates. pp. 622–625. ISBN 978-0-7167-2629-6.
  63. Sahney, S.; Benton, M.J.; Falcon-Lang, H.J. (2010). "Rainforest collapse triggered Pennsylvanian tetrapod diversification in Euramerica". Geology. 38 (12): 1079–1082. Bibcode:2010Geo....38.1079S. doi:10.1130/G31182.1.CS1 maint: ref=harv (link)
  64. Pearson, Marianne R.; Benson, Roger B.J.; Upchurch, Paul; Fröbisch, Jörg; Kammerer, Christian F. (2013). "Reconstructing the diversity of early terrestrial herbivorous tetrapods". Palaeogeography, Palaeoclimatology, Palaeoecology. 372: 42–49. Bibcode:2013PPP...372...42P. doi:10.1016/j.palaeo.2012.11.008.
  65. Sahney, S.; Benton, M.J. (2008). "Recovery from the most profound mass extinction of all time" (PDF). Proceedings of the Royal Society B: Biological Sciences. 275 (1636): 759–65. doi:10.1098/rspb.2007.1370. PMC 2596898. PMID 18198148.CS1 maint: ref=harv (link)
  66. Lehrmann, D.J.; Ramezan, J.; Bowring, S.A.; et al. (December 2006). "Timing of recovery from the end-Permian extinction: Geochronologic and biostratigraphic constraints from south China". Geology. 34 (12): 1053–6. Bibcode:2006Geo....34.1053L. doi:10.1130/G22827A.1.CS1 maint: ref=harv (link)
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