Secondarily aquatic tetrapods

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Several groups of tetrapods have undergone secondary aquatic adaptation, an evolutionary transition from being purely terrestrial to living at least part of the time in water. These animals are called "secondarily aquatic" because although their ancestors lived on land for hundreds of millions of years, they all originally descended from aquatic animals (see Evolution of tetrapods). These ancestral tetrapods had never left the water, and were thus primarily aquatic, like modern fishes. Secondary aquatic adaptations tend to develop in early speciation as the animal ventures into water in order to find available food. As successive generations spend more time in the water, natural selection causes the acquisition of more adaptations. Animals of later generations may spend most their life in the water, coming ashore for mating. Finally, fully adapted animals may take to mating and birthing in water or ice.

Contents

Marine Reptiles

Mesosaurs

Restoration of a mesosaurus, the earliest group of aquatic reptiles. Mesosaurus BW.jpg
Restoration of a mesosaurus, the earliest group of aquatic reptiles.

Mesosaurs were a group of small aquatic reptiles that lived during the early Permian period (Cisuralian), roughly 299 to 270 million years ago. Mesosaurs were the first known aquatic reptiles, having returned to an aquatic lifestyle from more terrestrial ancestors. [1] Most authors consider mesosaurs to have been fully aquatic, although adult animals may have been only semiaquatic. [2]

Turtles

Archelon is a type of giant sea turtle dating from the Cretaceous Period, now long extinct. Its smaller cousins survive as the sea turtles of today.

Squamates

Restoration of Mosasaurus hoffmannii, an extinct marine lizard. Mosasaurus 21copy.jpg
Restoration of Mosasaurus hoffmannii , an extinct marine lizard.

Squamata is the largest order of reptiles, comprising lizards, snakes, and amphisbaenians (worm lizards). There are many examples of aquatic squamates, both living and extinct; a secondarily aquatic lifestyle has evolved multiple times.

Living at the same time as, but not closely related to, dinosaurs, the mosasaurs resembled crocodiles but were more strongly adapted to marine life. Scientists continue to debate on whether monitor lizards [3] or snakes [4] are the closest living relatives of mosasaurs. Mosasaurs became extinct 66 million years ago, at the same time as the dinosaurs.

A modern semi-aquatic lizard: the marine iguana Marine iguana (4202531062).jpg
A modern semi-aquatic lizard: the marine iguana

Modern squamates which have made their own adaptions to allow them to spend significant time in the ocean include marine iguanas and sea snakes. Sea snakes are extensively adapted to the marine environment, giving birth to live offspring and are largely incapable of terrestrial activity. The arc of their adaptation is evident by observing the primitive Laticauda genus, which must return to land to lay eggs.

Ichthyosaurs

These marine reptiles had ancestors who moved back into the oceans. Ichthyosaurs adapted as fully as the dolphins they superficially resemble, even giving birth to live offspring instead of laying eggs.

Crocodilomorphs

Crocodilomorphs are a group of reptiles that include crocodilians and their extinct relatives. Many though not all crocodilomorphs had an aquatic or semiaquatic lifestyle. One group, the Metriorhynchidae displayed extreme adaptions for life in the open ocean, including the transformation of limbs into flippers, the development of a tail fluke, smooth, scaleless skin, [5] and probably even live birth. [6]

Life reconstruction of Aristonectes quiriquinensis, a pleisiosaur. Aristonectes NT small.jpg
Life reconstruction of Aristonectes quiriquinensis, a pleisiosaur.

Sauropterygians

Sauropterygians developed from terrestrial ancestors soon after the end-Permian extinction and flourished during the Triassic before all except for the Plesiosauria became extinct at the end of that period. The plesiosaurs went extinct at the Cretaceous–Paleogene extinction event, the same event which killed the non-avian dinosaurs. Sauropterygians include placodonts, nothosaurs, plesiosaurs, and pliosaurs.

Marine mammals

Cetacea

During the Paleocene Epoch (about 66 - 55 million years ago), the ancient whale Pakicetus began pursuing an amphibious lifestyle in rivers or shallow seas. It was the ancestor of modern whales, dolphins, and porpoises. The cetacea are extensively adapted to marine life and cannot survive on land at all. Their adaptation can be seen in many unique physiognomic characteristics such as the dorsal blowhole, baleen teeth, and the cranial 'melon' organ used for aquatic echolocation. The closest extant terrestrial relative to the whale is the hippopotamus, which spends much of its time in the water and whose name literally means "horse of the river".

Sirenians

The ancestors of the dugong and manatees first appeared in the fossil record about 45 to 50 million years ago in the ocean.

Pinnipeds

The fossil records show that phocids existed 12 to 15 million years ago, and odobenids about 14 million years ago. Their common ancestor must have existed even earlier than that.

Polar bears

Although polar bears spend most of their time on the ice rather than in the water, polar bears show the beginnings of aquatic adaptation to swimming (high levels of body fat and nostrils that are able to close), diving, and thermoregulation. Distinctly polar bear fossils can be dated to about 100,000 years ago. The polar bear has thick fur and layers of fat on its body to protect it from the cold.

Speculative theories

Humans

Proponents of the aquatic ape hypothesis believe that part of human evolution includes some aquatic adaptation, which has been said to explain human hairlessness, bipedalism, increased subcutaneous fat, descended larynx, vernix caseosa, a hooded nose and various other physiological and anatomical changes. The idea is not accepted by most scholars who study human evolution. [7]

See also

Related topics

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<span class="mw-page-title-main">Reptile</span> Group of animals including lepidosaurs, testudines, and archosaurs

Reptiles, as commonly defined, are a group of tetrapods with an ectothermic ('cold-blooded') metabolism and amniotic development. Living reptiles comprise four orders: Testudines (turtles), Crocodilia (crocodilians), Squamata, and Rhynchocephalia. As of May 2023, about 12,000 living species of reptiles are listed in the Reptile Database. The study of the traditional reptile orders, customarily in combination with the study of modern amphibians, is called herpetology.

<span class="mw-page-title-main">Tetrapod</span> Superclass of the first four-limbed vertebrates and their descendants

A tetrapod is any four-limbed vertebrate animal of the superclass Tetrapoda. Tetrapods include all extant and extinct amphibians and amniotes, with the latter in turn evolving into two major clades, the sauropsids and synapsids. Some tetrapods such as snakes, legless lizards, and caecilians had evolved to become limbless via mutations of the Hox gene, although some do still have a pair of vestigial spurs that are remnants of the hindlimbs.

<span class="mw-page-title-main">Amniote</span> Clade of tetrapods including reptiles, birds and mammals

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 amphibian ancestors during the Carboniferous period and further diverged into two groups, namely the sauropsids and synapsids. They are distinguished from the other living tetrapod clade — the non-amniote lissamphibians — by the development of three extraembryonic membranes, thicker and keratinized skin, and costal respiration.

<span class="mw-page-title-main">Squamata</span> Order of reptiles

Squamata is the largest order of reptiles, comprising lizards, snakes, and amphisbaenians, which are collectively known as squamates or scaled reptiles. With over 11,500 species, it is also the second-largest order of extant (living) vertebrates, after the perciform fish. Members of the order are distinguished by their skins, which bear horny scales or shields, and must periodically engage in molting. They also possess movable quadrate bones, making possible movement of the upper jaw relative to the neurocranium. This is particularly visible in snakes, which are able to open their mouths very wide to accommodate comparatively large prey. Squamates are the most variably sized living reptiles, ranging from the 16 mm (0.63 in) dwarf gecko to the 6.5 m (21 ft) reticulated python. The now-extinct mosasaurs reached lengths over 14 m (46 ft).

<span class="mw-page-title-main">Ophidia</span> Group of squamate reptiles

Ophidia is a group of squamate reptiles including modern snakes and reptiles more closely related to snakes than to other living groups of lizards.

<span class="mw-page-title-main">Marine reptile</span> Aquatically secondarily adapted reptiles

Marine reptiles are reptiles which have become secondarily adapted for an aquatic or semiaquatic life in a marine environment.

<span class="mw-page-title-main">Mosasaur</span> Extinct marine lizards of the Late Cretaceous

Mosasaurs comprise a group of extinct, large marine reptiles from the Late Cretaceous. Their first fossil remains were discovered in a limestone quarry at Maastricht on the Meuse in 1764. They belong to the order Squamata, which includes lizards and snakes.

<span class="mw-page-title-main">Sauropterygia</span> Group of Mesozoic aquatic reptiles

Sauropterygia is an extinct taxon of diverse, aquatic reptiles that developed from terrestrial ancestors soon after the end-Permian extinction and flourished during the Triassic before all except for the Plesiosauria became extinct at the end of that period. The plesiosaurs would continue to diversify until the end of the Mesozoic. Sauropterygians are united by a radical adaptation of their pectoral girdle, adapted to support powerful flipper strokes. Some later sauropterygians, such as the pliosaurs, developed a similar mechanism in their pelvis.

<span class="mw-page-title-main">Pythonomorpha</span> Clade of lizards

Pythonomorpha was originally proposed by paleontologist Edward Drinker Cope (1869) as a reptilian order comprising mosasaurs, which he believed to be close relatives of Ophidia (snakes). The etymology of the term Pythonomorpha comes from the Greek Python and morphe ("form"), and refers to the generally serpentine body plan of members of the group. Cope wrote, "In the mosasauroids, we almost realize the fictions of snake-like dragons and sea-serpents, in which men have been ever prone to indulge. On account of the ophidian part of their affinities, I have called this order Pythonomorpha." Cope incorporated two families, the Clidastidae and the Mosasauridae.

<span class="mw-page-title-main">Metriorhynchidae</span> Extinct family of reptiles

Metriorhynchidae is an extinct family of specialized, aquatic metriorhynchoid crocodyliforms from the Middle Jurassic to the Early Cretaceous period of Europe, North America and South America. The name Metriorhynchidae was coined by the Austrian zoologist Leopold Fitzinger in 1843. The group contains two subfamilies, the Metriorhynchinae and the Geosaurinae. They represent the most marine adapted of all archosaurs.

<i>Mesosaurus</i> Extinct genus of reptile from the early Permian of South Africa

Mesosaurus is an extinct genus of reptile from the Early Permian of southern Africa and South America. Along with it, the genera Brazilosaurus and Stereosternum, it is a member of the family Mesosauridae and the order Mesosauria. Mesosaurus was long thought to have been one of the first marine reptiles, although new data suggests that at least those of Uruguay inhabited a hypersaline water body, rather than a typical marine environment. In any case, it had many adaptations to a fully aquatic lifestyle. It is usually considered to have been anapsid, although Friedrich von Huene considered it to be a synapsid. Recent study of Mesosauridae phylogeny places the group as either the basal most clade within Parareptilia or the basal most clade within Sauropsida despite the skull of Mesosaurus possessing the "Synapsid condition" of one temporal fenestra.

<i>Dinilysia</i> Extinct genus of snakes

Dinilysia is an extinct genus of snake from the Late Cretaceous (Coniacian) of South America. Dinilysia was a relatively large ambush predator, measuring approximately 2 m (6.6 ft) long. The skull morphology of Dinilysia is similar to boids, suggesting that it was able to consume large prey. Living in a desert-like environment, Dinilysia is likely a terrestrial or a semi-fossorial animal.

<span class="mw-page-title-main">Marine vertebrate</span> Marine animals with a vertebrate column

Marine vertebrates are vertebrates that live in marine environments. These are the marine fish and the marine tetrapods. Vertebrates are a subphylum of chordates that have a vertebral column (backbone). The vertebral column provides the central support structure for an internal skeleton. The internal skeleton gives shape, support, and protection to the body and can provide a means of anchoring fins or limbs to the body. The vertebral column also serves to house and protect the spinal cord that lies within the column.

<i>Palaeopleurosaurus</i> Extinct genus of reptiles

Palaeopleurosaurus is an extinct genus of diapsid reptiles belonging to the group Sphenodontia.

<span class="mw-page-title-main">Evolution of reptiles</span> Origin and diversification of reptiles through geologic time

Reptiles arose about 320 million years ago during the Carboniferous period. Reptiles, in the traditional sense of the term, are defined as animals that have scales or scutes, lay land-based hard-shelled eggs, and possess ectothermic metabolisms. So defined, the group is paraphyletic, excluding endothermic animals like birds that are descended from early traditionally-defined reptiles. A definition in accordance with phylogenetic nomenclature, which rejects paraphyletic groups, includes birds while excluding mammals and their synapsid ancestors. So defined, Reptilia is identical to Sauropsida.

<span class="mw-page-title-main">Evolution of tetrapods</span> Evolution of four legged vertebrates and their derivatives

The evolution of tetrapods began about 400 million years ago in the Devonian Period with the earliest tetrapods evolved from lobe-finned fishes. Tetrapods 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. The specific aquatic ancestors of the tetrapods, and the process by which land colonization occurred, remain unclear. They are areas of active research and debate among palaeontologists at present.

<i>Megachirella</i> Extinct genus of reptiles

Megachirella is an extinct genus of lepidosaur, possibly a stem-squamate that lived about 240 million years ago during the Middle Triassic and contains only one known species, Megachirella wachtleri. It is known from a partial skeleton discovered in the Dolomites of Northern Italy and was described in 2003.

<i>Tetrapodophis</i> Extinct genus of lizard

Tetrapodophis is an extinct genus of lizard from the Early Cretaceous (Aptian) aged Crato Formation of Brazil. It has an elongate snake-like body, with four limbs. Tetrapodophis has been considered by some authors to be one of the oldest members of Ophidia. However, this classification has been disputed by some other authors, who identify Tetrapodophis as a dolichosaurid much less closely related to snakes.

<span class="mw-page-title-main">Dolichosauridae</span> Extinct family of lizards

Dolichosauridae is a family of Cretaceous aquatic ophidiomorphan lizards closely related to the snakes and mosasaurs.

References

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  2. Pablo Nuñez Demarco et al. Was Mesosaurus a Fully Aquatic Reptile? Front. Ecol. Evol, published online July 27, 2018; doi: 10.3389/fevo.2018.00109
  3. John J. Wiens; Caitlin A. Kuczynski; Ted Townsend; Tod W. Reeder; Daniel G. Mulcahy; Jack W. Sites Jr. (2012). "Combining Phylogenomics and Fossils in Higher-Level Squamate Reptile Phylogeny: Molecular Data Change the Placement of Fossil Taxa" (PDF). Systematic Biology. 59 (6): 674–88. doi:10.1093/sysbio/syq048. PMID   20930035.
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  5. Spindler, Frederik; Lauer, René; Tischlinger, Helmut; Mäuser, Matthias (2021-07-05). "The integument of pelagic crocodylomorphs (Thalattosuchia: Metriorhynchidae)". Palaeontologia Electronica. 24 (2): 1–41. doi: 10.26879/1099 . ISSN   1094-8074.
  6. Herrera, Y.; Fernandez, M.S.; Lamas, S.G.; Campos, L.; Talevi, M.; Gasparini, Z. (2017). "Morphology of the sacral region and reproductive strategies of Metriorhynchidae: a counter-inductive approach". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 106 (4): 247–255. doi: 10.1017/S1755691016000165 .
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