Chordate

Chordates Temporal range: Cambrian Stage 3–Present, 525–0 Ma[1] PreꞒ Ꞓ O S D C P T J K Pg N (Possible Ediacaran record, 555 Ma[2])
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Subkingdom:	Eumetazoa
Clade:	ParaHoxozoa
Clade:	Bilateria
Clade:	Nephrozoa
Superphylum:	Deuterostomia
Phylum:	Chordata Haeckel, 1874[3][4]
Subgroups
†Vetulocystidae?[5] †Vetulicolia? (Paraphyletic?)[6] †Yunnanozoon? †Cathaymyrus †Pikaia Cephalochordata Olfactores Tunicata Total group Vertebrata †Emmonsaspis[7] †Metaspriggina †Nuucichthys[7] †Myllokunmingiidae †Conodonta?[5] Vertebrata And see text

A chordate (/ˈkɔːrdeɪt/ KOR-dayt) is a deuterostomal bilaterian animal belonging to the phylum Chordata (/kɔːrˈdeɪtə/ kor-DAY-tə). All chordates possess, at some point during their larval or adult stages, five distinctive physical characteristics (synapomorphies) that distinguish them from other taxa. These five synapomorphies are a notochord, a hollow dorsal nerve cord, an endostyle or thyroid, pharyngeal slits, and a post-anal/post-cloacal tail.^[8]

In addition to the morphological characteristics used to define chordates, analysis of genome sequences has identified two conserved signature indels (CSIs) in their proteins: cyclophilin-like protein and inner mitochondrial membrane protease ATP23, which are exclusively shared by all vertebrates, tunicates and cephalochordates.^[9] These CSIs provide molecular means to reliably distinguish chordates from all other animals.

Chordates are divided into three subphyla: Vertebrata (fish, amphibians, reptiles, birds and mammals), whose notochords are replaced by a cartilaginous/bony axial endoskeleton (spine) and are cladistically and phylogenetically a subgroup of the clade Craniata (i.e. chordates with a skull); Tunicata or Urochordata (sea squirts, salps, and larvaceans), which only retain the synapomorphies during their larval stage; and Cephalochordata (lancelets), which resemble jawless fish but have no gills or a distinct head. The vertebrates and tunicates compose the clade Olfactores, which is sister to Cephalochordata (see diagram under Phylogeny). Extinct taxa such as the conodonts are chordates, but their internal placement is less certain. Hemichordata (which includes the acorn worms) was previously considered a fourth chordate subphylum, but now is treated as a separate phylum which are now thought to be closer to the echinoderms, and together they form the clade Ambulacraria, the sister phylum of the chordates. Chordata, Ambulacraria, and possibly Xenacoelomorpha are believed to form the superphylum Deuterostomia, although this has recently been called into doubt.^[10]

Chordata is the third-largest phylum of the animal kingdom (behind only the protostomal phyla Arthropoda and Mollusca) and is also one of the most ancient taxons. Chordate fossils have been found from as early as the Cambrian explosion over 539 million years ago.^[11] Of the more than 81,000^[12] living species of chordates, about half are ray-finned fishes (class Actinopterygii) and the vast majority of the rest are tetrapods, a terrestrial clade of lobe-finned fishes (Sarcopterygii) who evolved air-breathing using lungs.

The name "chordate" comes from the first of these synapomorphies, the notochord, which plays a significant role in chordate body plan structuring and movements. Chordates are also bilaterally symmetric, have a coelom, possess a closed circulatory system, and exhibit metameric segmentation. Although the name Chordata is attributed to William Bateson (1885), it was already in prevalent use by 1880. Ernst Haeckel described a taxon comprising tunicates, cephalochordates, and vertebrates in 1866. Though he used the German vernacular form, it is allowed under the ICZN code because of its subsequent latinization.^[4]

Chordates form a phylum of animals that are defined by having at some stage in their lives all of the following anatomical features:^[13]

• A notochord, a stiff but elastic rod of glycoprotein wrapped in two collagen helices, which extends along the central axis of the body. Among members of the subphylum Vertebrata (vertebrates), the notochord gets replaced by hyaline cartilage or osseous tissue of the spine, and notochord remnants develop into the intervertebral discs, which allow adjacent spinal vertebrae to bend and twist relative to each other. In wholly aquatic species, this helps the animal swim efficiently by flexing its tail side-to-side.
• A hollow dorsal nerve cord, also known as the neural tube, which develops into the spinal cord, the main communications trunk of the nervous system. In vertebrates, the rostral end of the neural tube enlarges into several vesicles during embryonic development, which give rise to the brain.
• Pharyngeal slits. The pharynx is the part of the throat immediately behind the mouth. In fish, the slits are modified to form gills, but in some other chordates they are part of a filter-feeding system that extracts food particles from ingested water. In tetrapods, they are only present during embryonic stages of the development.
• A tail. A muscular tail that extends backwards behind the anus or cloaca. In some chordates such as hominids, this is only present in the embryonic stage.
• An endostyle. This is a groove in the ventral wall of the pharynx. In filter-feeding species it produces mucus to gather food particles, which helps in transporting food to the esophagus.^[14] It also stores iodine, and may be a precursor of the vertebrate thyroid gland.^[13]

There are soft constraints that separate chordates from other biological lineages, but are not part of the formal definition:

• All chordates are deuterostomes. This means that, during embryonic development, the anus forms before the mouth does.
• All chordates are based on a bilateral body plan.^[15]
• All chordates are coelomates, and have a fluid-filled body cavity (coelom) with a complete serosal lining derived from mesoderm called mesothelium (see Brusca and Brusca).^[16]

1 = bulge in spinal cord ("brain")

2 = notochord

3 = dorsal nerve cord

4 = post-anal tail

5 = anus

6 = digestive canal

7 = circulatory system

8 = atriopore

9 = space above pharynx

10 = pharyngeal slit (gill)

11 = pharynx

12 = vestibule

13 = oral cirri

14 = mouth opening

15 = gonads (ovary / testicle)

16 = light sensor

17 = nerves

18 = metapleural fold

19 = hepatic caecum (liver-like sack)

Anatomy of the cephalochordate Branchiostoma lanceolatum. Bolded items are components of all chordates at some point in their lifetimes, and distinguish them from other phyla.

The following schema is from the 2015 edition of Vertebrate Palaeontology.^[17][18] The invertebrate chordate classes are from Fishes of the World.^[19] While it is structured so as to reflect evolutionary relationships (similar to a cladogram), it also retains the traditional ranks used in Linnaean taxonomy.

• Phylum Chordata
  • Subphylum Cephalochordata (Acraniata) – (lancelets; 30 species)
    • Class Leptocardii (lancelets)
  • Clade Olfactores
    • Subphylum Tunicata (Urochordata) – (tunicates; 3,000 species)
      • Class Ascidiacea (sea squirts)
      • Class Thaliacea (salps, doliolids and pyrosomes)
      • Class Appendicularia (larvaceans)
    • Subphylum Vertebrata (Craniata) (vertebrates – animals with backbones; 66,100+ species)
      • Superclass 'Agnatha' paraphyletic (jawless vertebrates; 100+ species)
        • Class Cyclostomata
          • Infraclass Myxinoidea or Myxini (hagfish; 65 species)
          • Infraclass Petromyzontida or Hyperoartia (lampreys)
        • Class †Conodonta
        • Class †Myllokunmingiida
        • Class †Pteraspidomorphi
        • Class †Thelodonti
        • Class †Anaspida
        • Class †Cephalaspidomorphi
      • Infraphylum Gnathostomata (jawed vertebrates)
        • Class †Placodermi (Paleozoic armoured forms; paraphyletic in relation to all other gnathostomes)
        • Class Chondrichthyes (cartilaginous fish; 900+ species)
        • Class †Acanthodii (Paleozoic "spiny sharks"; paraphyletic in relation to Chondrichthyes)
        • Class Osteichthyes (bony fish; 30,000+ species)
          • Subclass Actinopterygii (ray-finned fish; about 30,000 species)
          • Subclass Sarcopterygii (lobe-finned fish: 8 species)
        • Superclass Tetrapoda (four-limbed vertebrates; 35,100+ species) (The classification below follows Benton 2004, and uses a synthesis of rank-based Linnaean taxonomy and also reflects evolutionary relationships. Benton included the superclass Tetrapoda in the subclass Sarcopterygii in order to reflect the direct descent of tetrapods from lobe-finned fish, despite the former being assigned a higher taxonomic rank.)^[20]
          • Class Amphibia (amphibians; 8,100+ species)^[21]
          • Class Sauropsida (reptiles (including birds); 21,300+ species – 10,000+ species of birds and 11,300+ species of reptiles)^[22][23][24]
          • Class Synapsida (mammals; 5,700+ species)

Cephalochordates, one of the three subdivisions of chordates, are small, "vaguely fish-shaped" animals that lack brains, clearly defined heads and specialized sense organs.^[25] These burrowing filter-feeders compose the earliest-branching chordate subphylum.^[26][27]

The tunicates have three distinct adult shapes. Each is a member of one of three monophylitic clades. All tunicate larvae have the standard chordate features, including long, tadpole-like tails. Their larva also have rudimentary brains, light sensors and tilt sensors.^[28]

The smallest of the three groups of tunicates is the Appendicularia. They retain tadpole-like shapes and active swimming all their lives, and were for a long time regarded as larvae of the other two groups.^[29]

The other two groups, the sea squirts and the salps, metamorphize into adult forms which lose the notochord, nerve cord, and post anal tail. Both are soft-bodied filter feeders with multiple gill slits. They feed on plankton which they collect in their mucus.

Sea squirts are sessile and consist mainly of water pumps and filter-feeding apparatus.^[28] Most attach firmly to the sea floor, where they remain in one place for life, feeding on plankton.

The salps float in mid-water, feeding on plankton, and have a two-generation cycle in which one generation is solitary and the next forms chain-like colonies.^[30]

The etymology of the term Urochordata (Balfour 1881) is from the ancient Greek οὐρά (oura, "tail") + Latin chorda ("cord"), because the notochord is only found in the tail.^[31] The term Tunicata (Lamarck 1816) is recognised as having precedence and is now more commonly used.^[28]

Comparison of two invertebrate chordates

A. Lancelet, B. Larval tunicate, C. Adult tunicate
--------------------------------------------------------
1. Notochord, 2. Nerve chord, 3. Buccal cirri, 4. Pharynx, 5. Gill slit, 6. Gonad, 7. Gut, 8. V-shaped muscles, 9. Anus, 10. Inhalant syphon, 11. Exhalant syphon, 12. Heart, 13. Stomach, 14. Esophagus, 15. Intestines, 16. Tail, 17. Atrium, 18. Tunic

Craniates all have distinct skulls. They include the hagfish, which have no vertebrae. Michael J. Benton commented that "craniates are characterized by their heads, just as chordates, or possibly all deuterostomes, are by their tails".^[32]

Most craniates are vertebrates, in which the notochord is replaced by the vertebral column.^[33] It consists of a series of bony or cartilaginous cylindrical vertebrae, generally with neural arches that protect the spinal cord, and with projections that link the vertebrae. Hagfishes have incomplete braincases and no vertebrae, and are therefore not regarded as vertebrates,^[34] but they are members of the craniates, the group within which vertebrates are thought to have evolved.^[35] However the cladistic exclusion of hagfish from the vertebrates is controversial, as they may instead be degenerate vertebrates who have secondarily lost their vertebral columns.^[36]

Before molecular phylogenetics, the position of lampreys was ambiguous. They have complete braincases and rudimentary vertebrae, and therefore may be regarded as vertebrates and true fish.^[37] However, molecular phylogenetics, which uses DNA to classify organisms, has produced both results that group them with vertebrates and others that group them with hagfish.^[38] If lampreys are more closely related to the hagfish than the other vertebrates, this would suggest that they form a clade, which has been named the Cyclostomata.^[39]

There is still much ongoing differential (DNA sequence based) comparison research that is trying to separate out the simplest forms of chordates. As some lineages of the 90% of species that lack a backbone or notochord might have lost these structures over time, this complicates the classification of chordates. Some chordate lineages may only be found by DNA analysis, when there is no physical trace of any chordate-like structures.^[41]

Attempts to work out the evolutionary relationships of the chordates have produced several hypotheses. The current consensus is that chordates are monophyletic, meaning that the Chordata include all and only the descendants of a single common ancestor, which is itself a chordate, and that craniates' nearest relatives are tunicates. Recent identification of two conserved signature indels (CSIs) in the proteins cyclophilin-like protein and mitochondrial inner membrane protease ATP23, which are exclusively shared by all vertebrates, tunicates and cephalochordates also provide strong evidence of the monophyly of Chordata.^[9]

All of the earliest chordate fossils have been found in the Early Cambrian Chengjiang fauna, and include two species that are regarded as fish, which implies that they are vertebrates. Because the fossil record of early chordates is poor, only molecular phylogenetics offers a reasonable prospect of dating their emergence. However, the use of molecular phylogenetics for dating evolutionary transitions is controversial.

It has also proved difficult to produce a detailed classification within the living chordates. Attempts to produce evolutionary "family trees" shows that many of the traditional classes are paraphyletic.

While this has been well known since the 19th century, an insistence on only monophyletic taxa has resulted in vertebrate classification being in a state of flux.^[42]

The majority of animals more complex than jellyfish and other cnidarians are split into two groups, the protostomes and deuterostomes, the latter of which contains chordates.^[43] It seems very likely the 555 million-year-old Kimberella was a member of the protostomes.^[44][45] If so, this means the protostome and deuterostome lineages must have split some time before Kimberella appeared—at least 558 million years ago, and hence well before the start of the Cambrian 538.8 million years ago.^[43] Three enigmatic species that are possible very early tunicates, and therefor deuterostomes, were also found from the Ediacaran period – Ausia fenestrata from the Nama Group of Namibia, the sac-like Yarnemia ascidiformis, and one from a second new Ausia-like genus from the Onega Peninsula of northern Russia, Burykhia hunti. Results of a new study have shown possible affinity of these Ediacaran organisms to the ascidians.^[46][47] Ausia and Burykhia lived in shallow coastal waters slightly more than 555 to 548 million years ago, and are believed to be the oldest evidence of the chordate lineage of metazoans.^[47] The Russian Precambrian fossil Yarnemia is identified as a tunicate only tentatively, because its fossils are nowhere near as well-preserved as those of Ausia and Burykhia, so this identification has been questioned.

Fossils of one major deuterostome group, the echinoderms (whose modern members include starfish, sea urchins and crinoids), are quite common from the start of the Cambrian, 542 million years ago.^[48] The Mid Cambrian fossil Rhabdotubus johanssoni has been interpreted as a pterobranch hemichordate.^[49] Opinions differ about whether the Chengjiang fauna fossil Yunnanozoon, from the earlier Cambrian, was a hemichordate or chordate.^[50][51] Another fossil, Haikouella lanceolata, also from the Chengjiang fauna, is interpreted as a chordate and possibly a craniate, as it shows signs of a heart, arteries, gill filaments, a tail, a neural chord with a brain at the front end, and possibly eyes—although it also had short tentacles round its mouth.^[51] Haikouichthys and Myllokunmingia, also from the Chengjiang fauna, are regarded as fish.^[40][52] Pikaia, discovered much earlier (1911) but from the Mid Cambrian Burgess Shale (505 Ma), is also regarded as a primitive chordate.^[53] On the other hand, fossils of early chordates are very rare, since invertebrate chordates have no bones or teeth, and only one has been reported for the rest of the Cambrian.^[54] The best known and earliest unequivocally identified Tunicate is Shankouclava shankouense from the Lower Cambrian Maotianshan Shale at Shankou village, Anning, near Kunming (South China).^[55]

The evolutionary relationships between the chordate groups and between chordates as a whole and their closest deuterostome relatives have been debated since 1890. Studies based on anatomical, embryological, and paleontological data have produced different "family trees". Some closely linked chordates and hemichordates, but that idea is now rejected.^[14] Combining such analyses with data from a small set of ribosome RNA genes eliminated some older ideas, but opened up the possibility that tunicates (urochordates) are "basal deuterostomes", surviving members of the group from which echinoderms, hemichordates and chordates evolved.^[56] Some researchers believe that, within the chordates, craniates are most closely related to cephalochordates, but there are also reasons for regarding tunicates (urochordates) as craniates' closest relatives.^[14][57]

Since early chordates have left a poor fossil record, attempts have been made to calculate the key dates in their evolution by molecular phylogenetics techniques—by analyzing biochemical differences, mainly in RNA. One such study suggested that deuterostomes arose before 900 million years ago and the earliest chordates around 896 million years ago.^[57] However, molecular estimates of dates often disagree with each other and with the fossil record,^[57] and their assumption that the molecular clock runs at a known constant rate has been challenged.^[58][59]

Traditionally, Cephalochordata and Craniata were grouped into the proposed clade "Euchordata", which would have been the sister group to Tunicata/Urochordata. More recently, Cephalochordata has been thought of as a sister group to the "Olfactores", which includes the craniates and tunicates. The matter is not yet settled.

A specific relationship between vertebrates and tunicates is also strongly supported by two CSIs found in the proteins predicted exosome complex RRP44 and serine palmitoyltransferase, that are exclusively shared by species from these two subphyla but not cephalochordates, indicating vertebrates are more closely related to tunicates than cephalochordates.^[9]

Below is a phylogenetic tree of the phylum. Lines of the cladogram show probable evolutionary relationships between both extinct taxa, which are denoted with a dagger (†), and extant taxa.^{[60][61][62][63][64]}

The closest relatives of the chordates are believed to be the hemichordates and Echinodermata, which together form the Ambulacraria. The Chordata and Ambulacraria together form the superphylum Deuterostomia.

Hemichordates ("half chordates") have some features similar to those of chordates: branchial openings that open into the pharynx and look rather like gill slits; stomochords, similar in composition to notochords, but running in a circle round the "collar", which is ahead of the mouth; and a dorsal nerve cord—but also a smaller ventral nerve cord.

There are two living groups of hemichordates. The solitary enteropneusts, commonly known as "acorn worms", have long proboscises and worm-like bodies with up to 200 branchial slits, are up to 2.5 metres (8.2 ft) long, and burrow though seafloor sediments. Pterobranchs are colonial animals, often less than 1 millimetre (0.039 in) long individually, whose dwellings are interconnected. Each filter feeds by means of a pair of branched tentacles, and has a short, shield-shaped proboscis. The extinct graptolites, colonial animals whose fossils look like tiny hacksaw blades, lived in tubes similar to those of pterobranchs.^[65]

Echinoderms differ from chordates and their other relatives in three conspicuous ways: they possess bilateral symmetry only as larvae – in adulthood they have radial symmetry, meaning that their body pattern is shaped like a wheel; they have tube feet; and their bodies are supported by dermal skeletons made of calcite, a material not used by chordates. Their hard, calcified shells keep their bodies well protected from the environment, and these skeletons enclose their bodies, but are also covered by thin skins. The feet are powered by another unique feature of echinoderms, a water vascular system of canals that also functions as a "lung" and surrounded by muscles that act as pumps. Crinoids are typically sessile and look rather like flowers (hence the common name "sea lilies"), and use their feather-like arms to filter food particles out of the water; most live anchored to rocks, but a few species can move very slowly. Other echinoderms are mobile and take a variety of body shapes, for example starfish and brittle stars, sea urchins and sea cucumbers.^[66]

• Chordate genomics
• List of chordate orders – All the classes and orders of phylum Chordata

Wikispecies has information related to Chordata.

The Wikibook Dichotomous Key has a page on the topic of: Chordata

• "Chordate". The Encyclopedia of Life.
• Chordate on GlobalTwitcher.com
• Chordate node at Tree Of Life
• Chordate node at NCBI Taxonomy