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Chordate

A chordate (/ˈkɔːrdt/) is an animal of the phylum Chordata (/kɔːrˈdtə/). All chordates possess, at some point during their larval or adult stages, five synapomorphies, or primary physical characteristics, that distinguish them from all the other taxa. These five synapomorphies include a notochord, dorsal hollow nerve cord, endostyle or thyroid, pharyngeal slits, and a post-anal tail. The name “chordate” comes from the first of these synapomorphies, the notochord, which plays a significant role in chordate structure and movement. Chordates are also bilaterally symmetric, have a coelom, possess a circulatory system, and exhibit metameric segmentation.

Chordates
Temporal range: Cambrian Stage 3Present, 518–0 Ma[1] (Possible Ediacaran record, 555 Ma[2])
Branchiostoma lanceolatumPolycarpa aurataTiger sharkSiberian tiger
Example of chordates: Branchiostoma lanceolatum (Cephalochordata), Polycarpa aurata (Tunicata), as well as a Tiger shark and a Siberian tiger (Vertebrata).
Scientific classification
Kingdom: Animalia
Subkingdom: Eumetazoa
Clade: ParaHoxozoa
Clade: Bilateria
Clade: Nephrozoa
Superphylum: Deuterostomia
Phylum: Chordata
Haeckel, 1874[3][4]
Subgroups

And see text

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 mitochondrial inner membrane protease ATP23, which are exclusively shared by all vertebrates, tunicates and cephalochordates.[5] These CSIs provide molecular means to reliably distinguish chordates from all other metazoan.

Chordates are divided into three subphyla: Craniata (fish, amphibians, reptiles, birds, and mammals); Tunicata or Urochordata (sea squirts, salps); and Cephalochordata (which includes lancelets). The Craniata and Tunicata compose the clade Olfactores, which is sister to Cephalochordata. (See diagram under Phylogeny.) Extinct taxa such as Vetulicolia and Conodonta are Chordata, 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: hemichordates and Echinodermata form the Ambulacraria, the sister phylum of the Chordates. The Chordata and Ambulacraria, together and possibly with the Xenacoelomorpha, form the superphylum Deuterostomia.

Chordate fossils have been found from as early as the Cambrian explosion, 539 million years ago.[6] Cladistically (phylogenetically), vertebrates – chordates with the notochord replaced by a vertebral column during development – are a subgroup of the clade Craniata, which consists of chordates with a skull. Of the more than 65,000 living species of chordates, about half are ray-finned fishes that are members of the class Actinopterygii and the vast majority of the rest are tetrapods (mostly birds and mammals).

Anatomy

 
The glass catfish (Kryptopterus vitreolus) is one of the few chordates with a visible backbone. The spinal cord is housed within its backbone.

Chordates form a phylum of animals that are defined by having at some stage in their lives all of the following anatomical features:[7]

  • A notochord, a stiff rod of cartilage that extends along the inside of the body. Among the vertebrate sub-group of chordates the notochord develops into the spine, and in wholly aquatic species this helps the animal to swim by flexing its tail.
  • A dorsal neural tube. In fish and other vertebrates, this develops into the spinal cord, the main communications trunk of the nervous system.
  • 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 particles of food from the water in which the animals live. In tetrapods, they are only present during embryonic stages of the development.
  • Post-anal tail. A muscular tail that extends backwards behind the anus. In some chordates such as humans, 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.[8] It also stores iodine, and may be a precursor of the vertebrate thyroid gland.[7]

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

 
1 = bulge in spinal cord ("brain")
4 = post-anal tail
5 = anus
9 = space above pharynx
11 = pharynx
12 = vestibule
13 = oral cirri
14 = mouth opening
16 = light sensor
17 = nerves
18 = metapleural fold
19 = hepatic caecum (liver-like sack)
 
Anatomy of the cephalochordate Amphioxus. Bolded items are components of all chordates at some point in their lifetimes, and distinguish them from other phyla.

Classification

The following schema is from the 2015 edition of Vertebrate Palaeontology.[11][12] The invertebrate chordate classes are from Fishes of the World.[13] While it is structured so as to reflect evolutionary relationships (similar to a cladogram), it also retains the traditional ranks used in Linnaean taxonomy.

Subphyla

 
Cephalochordate: Lancelet

Cephalochordata: Lancelets

Cephalochordates, one of the three subdivisions of chordates, are small, "vaguely fish-shaped" animals that lack brains, clearly defined heads and specialized sense organs.[19] These burrowing filter-feeders compose the earliest-branching chordate sub-phylum.[20][21]

Tunicata (Urochordata)

 
Tunicates: sea squirts

Most tunicates appear as adults in two major forms, known as "sea squirts" and salps, both of which are soft-bodied filter-feeders that lack the standard features of chordates. Sea squirts are sessile and consist mainly of water pumps and filter-feeding apparatus;[22] 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.[23] However, all tunicate larvae have the standard chordate features, including long, tadpole-like tails; they also have rudimentary brains, light sensors and tilt sensors.[22] The third main group of tunicates, Appendicularia (also known as Larvacea), retain tadpole-like shapes and active swimming all their lives, and were for a long time regarded as larvae of sea squirts or salps.[24] 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.[25] The term Tunicata (Lamarck 1816) is recognised as having precedence and is now more commonly used.[22]

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

Craniata (Vertebrata)

 
Craniate: Hagfish

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".[26]

Most craniates are vertebrates, in which the notochord is replaced by the vertebral column.[27] These consist 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. However hagfish have incomplete braincases and no vertebrae, and are therefore not regarded as vertebrates,[28] but as members of the craniates, the group from which vertebrates are thought to have evolved.[29] However the cladistic exclusion of hagfish from the vertebrates is controversial, as they may be degenerate vertebrates who have lost their vertebral columns.[30]

The position of lampreys is ambiguous. They have complete braincases and rudimentary vertebrae, and therefore may be regarded as vertebrates and true fish.[31] However, molecular phylogenetics, which uses biochemical features to classify organisms, has produced both results that group them with vertebrates and others that group them with hagfish.[32] 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.[33]

Phylogeny

Overview

 
Haikouichthys, from about 518 million years ago in China, may be the earliest known fish.[34]

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.[35]

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.[5]

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.

Diagram of the evolutionary relationships of chordates[8]

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.[36]

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.[37] It seems very likely the 555 million-year-old Kimberella was a member of the protostomes.[38][39] 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.[37] The Ediacaran fossil Ernietta, from about 549 to 543 million years ago, may represent a deuterostome animal.[40]

 
A skeleton of the blue whale, the largest animal, extant or extinct, ever discovered, outside the Long Marine Laboratory at the University of California, Santa Cruz. The largest blue whale ever reliably recorded measured 98ft (29.9m) long.
 
A peregrine falcon, the world's fastest animal. Peregrines use gravity and aerodynamics to achieve their top speed of around 242mph (389km/h), as opposed to locomotion.

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.[41] The Mid Cambrian fossil Rhabdotubus johanssoni has been interpreted as a pterobranch hemichordate.[42] Opinions differ about whether the Chengjiang fauna fossil Yunnanozoon, from the earlier Cambrian, was a hemichordate or chordate.[43][44] 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.[44] Haikouichthys and Myllokunmingia, also from the Chengjiang fauna, are regarded as fish.[34][45] Pikaia, discovered much earlier (1911) but from the Mid Cambrian Burgess Shale (505 Ma), is also regarded as a primitive chordate.[46] 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.[47]

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.[8] 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.[48] 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.[8][49]

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.[49] However, molecular estimates of dates often disagree with each other and with the fossil record,[49] and their assumption that the molecular clock runs at a known constant rate has been challenged.[50][51]

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.[5]

Cladogram

Phylogenetic tree of the chordate phylum. Lines of the cladogram show probable evolutionary relationships between both extinct taxa, which are denoted with a dagger (†), and extant taxa. Relatives of vertebrates are invertebrates. The positions (relationships) of the lancelets, tunicates, and craniates/vertebrates are based on the following studies:[52][53][54][55]

Chordata
Cephalochordata

Amphioxiformes (lancelets)  

Olfactores

Haikouella

Tunicata

Appendicularia (formerly Larvacea)

"Ascidiacea" (polyphyletic; sea squirts)  

Thaliacea (salps)  

Vertebrata/

Conodonta  

Pteraspidomorphi (includes †Arandaspida, †Astraspida and †Heterostraci)  

Cephalaspidomorphi (includes †Galeaspida, †Osteostraci and †Pituriaspida)  

Gnathostomata

†"Placodermi" (paraphyletic; includes †Antiarchi, †Petalichthyida, †Ptyctodontida and †Arthrodira)  

Crown

†"Acanthodii" (paraphyletic)  

Chondrichthyes/Cartilaginous fishes (sharks, rays, rat fish)  

Euteleostomi/

Actinopterygii (ray-finned fishes)  

Sarcopterygii

Actinistia (coelacanths)  

Dipnoi (lungfishes)  

 Tetrapoda 
(four‑limbed vertebrates)
(lobe‑finned fishes)
Osteichthyes
Gnathostomata
Craniata

Closest nonchordate relatives

 
Acorn worms or Enteropneusts are example of hemichordates.

The closest relatives of the Chordates are the Hemichordates and Echinodermata, which together form the Ambulacraria. The Chordata and Ambulacraria together form the superphylum Deuterostomia.

Hemichordates

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.[56]

Echinoderms

 
A red knob sea star, Protoreaster linckii is an example of Asterozoan Echinoderm.

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 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 look rather like flowers, and use their feather-like arms to filter food particles out of the water; most live anchored to rocks, but a few can move very slowly. Other echinoderms are mobile and take a variety of body shapes, for example starfish, sea urchins and sea cucumbers.[57]

History of name

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]

See also

References

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External links

  • "Chordate" at the Encyclopedia of Life  
  • Chordate node at Tree Of Life
  • Chordate node at NCBI Taxonomy

chordate, confused, with, cordate, chordate, ɔːr, animal, phylum, chordata, ɔːr, chordates, possess, some, point, during, their, larval, adult, stages, five, synapomorphies, primary, physical, characteristics, that, distinguish, them, from, other, taxa, these,. Not to be confused with Cordate A chordate ˈ k ɔːr d eɪ t is an animal of the phylum Chordata k ɔːr ˈ d eɪ t e All chordates possess at some point during their larval or adult stages five synapomorphies or primary physical characteristics that distinguish them from all the other taxa These five synapomorphies include a notochord dorsal hollow nerve cord endostyle or thyroid pharyngeal slits and a post anal tail The name chordate comes from the first of these synapomorphies the notochord which plays a significant role in chordate structure and movement Chordates are also bilaterally symmetric have a coelom possess a circulatory system and exhibit metameric segmentation ChordatesTemporal range Cambrian Stage 3 Present 518 0 Ma 1 PreꞒ Ꞓ O S D C P T J K Pg N Possible Ediacaran record 555 Ma 2 Example of chordates Branchiostoma lanceolatum Cephalochordata Polycarpa aurata Tunicata as well as a Tiger shark and a Siberian tiger Vertebrata Scientific classificationKingdom AnimaliaSubkingdom EumetazoaClade ParaHoxozoaClade BilateriaClade NephrozoaSuperphylum DeuterostomiaPhylum ChordataHaeckel 1874 3 4 SubgroupsCephalochordata Pikaiidae Metaspriggiidae Olfactores Tunicata Vertebrata Zhongxiniscus YunnanozoonAnd see textIn 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 mitochondrial inner membrane protease ATP23 which are exclusively shared by all vertebrates tunicates and cephalochordates 5 These CSIs provide molecular means to reliably distinguish chordates from all other metazoan Chordates are divided into three subphyla Craniata fish amphibians reptiles birds and mammals Tunicata or Urochordata sea squirts salps and Cephalochordata which includes lancelets The Craniata and Tunicata compose the clade Olfactores which is sister to Cephalochordata See diagram under Phylogeny Extinct taxa such as Vetulicolia and Conodonta are Chordata 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 hemichordates and Echinodermata form the Ambulacraria the sister phylum of the Chordates The Chordata and Ambulacraria together and possibly with the Xenacoelomorpha form the superphylum Deuterostomia Chordate fossils have been found from as early as the Cambrian explosion 539 million years ago 6 Cladistically phylogenetically vertebrates chordates with the notochord replaced by a vertebral column during development are a subgroup of the clade Craniata which consists of chordates with a skull Of the more than 65 000 living species of chordates about half are ray finned fishes that are members of the class Actinopterygii and the vast majority of the rest are tetrapods mostly birds and mammals Contents 1 Anatomy 2 Classification 3 Subphyla 3 1 Cephalochordata Lancelets 3 2 Tunicata Urochordata 3 3 Craniata Vertebrata 4 Phylogeny 4 1 Overview 4 2 Cladogram 5 Closest nonchordate relatives 5 1 Hemichordates 5 2 Echinoderms 6 History of name 7 See also 8 References 9 External linksAnatomy Edit The glass catfish Kryptopterus vitreolus is one of the few chordates with a visible backbone The spinal cord is housed within its backbone Chordates form a phylum of animals that are defined by having at some stage in their lives all of the following anatomical features 7 A notochord a stiff rod of cartilage that extends along the inside of the body Among the vertebrate sub group of chordates the notochord develops into the spine and in wholly aquatic species this helps the animal to swim by flexing its tail A dorsal neural tube In fish and other vertebrates this develops into the spinal cord the main communications trunk of the nervous system 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 particles of food from the water in which the animals live In tetrapods they are only present during embryonic stages of the development Post anal tail A muscular tail that extends backwards behind the anus In some chordates such as humans 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 8 It also stores iodine and may be a precursor of the vertebrate thyroid gland 7 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 the embryo development stage the anus forms before the mouth All chordates are based on a bilateral body plan 9 All chordates are coelomates and have a fluid filled body cavity called a coelom with a complete lining called peritoneum derived from mesoderm see Brusca and Brusca 10 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 Amphioxus Bolded items are components of all chordates at some point in their lifetimes and distinguish them from other phyla Classification EditThe following schema is from the 2015 edition of Vertebrate Palaeontology 11 12 The invertebrate chordate classes are from Fishes of the World 13 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 Class Appendicularia larvaceans Class Sorberacea 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 14 Class Amphibia amphibians 8 100 species 15 Class Sauropsida reptiles including birds 21 300 species 10 000 species of birds and 11 300 species of reptiles 16 17 18 Class Synapsida mammals 5 700 species Subphyla EditSee also List of chordate orders Cephalochordate Lancelet Cephalochordata Lancelets Edit Main article Lancelet Cephalochordates one of the three subdivisions of chordates are small vaguely fish shaped animals that lack brains clearly defined heads and specialized sense organs 19 These burrowing filter feeders compose the earliest branching chordate sub phylum 20 21 Tunicata Urochordata Edit Main article Tunicate Urochordata Tunicates sea squirts Most tunicates appear as adults in two major forms known as sea squirts and salps both of which are soft bodied filter feeders that lack the standard features of chordates Sea squirts are sessile and consist mainly of water pumps and filter feeding apparatus 22 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 23 However all tunicate larvae have the standard chordate features including long tadpole like tails they also have rudimentary brains light sensors and tilt sensors 22 The third main group of tunicates Appendicularia also known as Larvacea retain tadpole like shapes and active swimming all their lives and were for a long time regarded as larvae of sea squirts or salps 24 The etymology of the term Urochordata Balfour 1881 is from the ancient Greek oὐra oura tail Latin chorda cord because the notochord is only found in the tail 25 The term Tunicata Lamarck 1816 is recognised as having precedence and is now more commonly used 22 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 Craniata Vertebrata Edit Main articles Craniata and Vertebrata Craniate Hagfish 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 26 Most craniates are vertebrates in which the notochord is replaced by the vertebral column 27 These consist 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 However hagfish have incomplete braincases and no vertebrae and are therefore not regarded as vertebrates 28 but as members of the craniates the group from which vertebrates are thought to have evolved 29 However the cladistic exclusion of hagfish from the vertebrates is controversial as they may be degenerate vertebrates who have lost their vertebral columns 30 The position of lampreys is ambiguous They have complete braincases and rudimentary vertebrae and therefore may be regarded as vertebrates and true fish 31 However molecular phylogenetics which uses biochemical features to classify organisms has produced both results that group them with vertebrates and others that group them with hagfish 32 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 33 Phylogeny EditOverview Edit Haikouichthys from about 518 million years ago in China may be the earliest known fish 34 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 35 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 5 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 Deuterostomes Ambulacraria Hemichordates Echinoderms Chordates Cephalochordates Olfactores Tunicates Craniates vertebrates Diagram of the evolutionary relationships of chordates 8 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 36 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 37 It seems very likely the 555 million year old Kimberella was a member of the protostomes 38 39 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 37 The Ediacaran fossil Ernietta from about 549 to 543 million years ago may represent a deuterostome animal 40 A skeleton of the blue whale the largest animal extant or extinct ever discovered outside the Long Marine Laboratory at the University of California Santa Cruz The largest blue whale ever reliably recorded measured 98ft 29 9m long A peregrine falcon the world s fastest animal Peregrines use gravity and aerodynamics to achieve their top speed of around 242mph 389km h as opposed to locomotion 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 41 The Mid Cambrian fossil Rhabdotubus johanssoni has been interpreted as a pterobranch hemichordate 42 Opinions differ about whether the Chengjiang fauna fossil Yunnanozoon from the earlier Cambrian was a hemichordate or chordate 43 44 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 44 Haikouichthys and Myllokunmingia also from the Chengjiang fauna are regarded as fish 34 45 Pikaia discovered much earlier 1911 but from the Mid Cambrian Burgess Shale 505 Ma is also regarded as a primitive chordate 46 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 47 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 8 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 48 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 8 49 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 49 However molecular estimates of dates often disagree with each other and with the fossil record 49 and their assumption that the molecular clock runs at a known constant rate has been challenged 50 51 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 5 Cladogram Edit Phylogenetic tree of the chordate phylum Lines of the cladogram show probable evolutionary relationships between both extinct taxa which are denoted with a dagger and extant taxa Relatives of vertebrates are invertebrates The positions relationships of the lancelets tunicates and craniates vertebrates are based on the following studies 52 53 54 55 Chordata Cephalochordata Amphioxiformes lancelets Olfactores HaikouellaTunicata Appendicularia formerly Larvacea Ascidiacea polyphyletic sea squirts Thaliacea salps Vertebrata Cyclostomata Myxini hagfishes Hyperoartia Petromyzontida lampreys Agnathans Conodonta Pteraspidomorphi includes Arandaspida Astraspida and Heterostraci Cephalaspidomorphi includes Galeaspida Osteostraci and Pituriaspida Gnathostomata Placodermi paraphyletic includes Antiarchi Petalichthyida Ptyctodontida and Arthrodira Crown Acanthodii paraphyletic Chondrichthyes Cartilaginous fishes sharks rays rat fish Euteleostomi Actinopterygii ray finned fishes Sarcopterygii Actinistia coelacanths Dipnoi lungfishes Tetrapoda Amphibia Amniota Synapsida Mammalia Sauropsida Lepidosauromorpha lizards snakes tuatara and their extinct relatives Archosauromorpha crocodiles birds and their extinct relatives Testudinata turtles and their extinct relatives four limbed vertebrates lobe finned fishes OsteichthyesGnathostomataCraniataClosest nonchordate relatives Edit Acorn worms or Enteropneusts are example of hemichordates The closest relatives of the Chordates are the Hemichordates and Echinodermata which together form the Ambulacraria The Chordata and Ambulacraria together form the superphylum Deuterostomia Hemichordates Edit Main article Hemichordate 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 56 Echinoderms Edit A red knob sea star Protoreaster linckii is an example of Asterozoan Echinoderm Main article Echinoderm 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 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 look rather like flowers and use their feather like arms to filter food particles out of the water most live anchored to rocks but a few can move very slowly Other echinoderms are mobile and take a variety of body shapes for example starfish sea urchins and sea cucumbers 57 History of name EditAlthough 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 See also EditChordate genomics List of chordate orders All the classes and orders of phylum ChordataReferences Edit Yang Chuan Li Xian Hua Zhu Maoyan Condon Daniel J Chen Junyuan 2018 Geochronological constraint on the Cambrian Chengjiang biota South China PDF Journal of the Geological Society 175 4 659 666 Bibcode 2018JGSoc 175 659Y doi 10 1144 jgs2017 103 ISSN 0016 7649 S2CID 135091168 Archived PDF from the original on 9 October 2022 Fedonkin M A Vickers Rich P Swalla B J Trusler P Hall M 2012 A new metazoan from the Vendian of the White Sea Russia with possible affinities to the ascidians Paleontological Journal 46 1 11 doi 10 1134 S0031030112010042 S2CID 128415270 Haeckel E 1874 Anthropogenie oder Entwicklungsgeschichte des Menschen Leipzig Engelmann a b Nielsen C 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