Ceratobranchial Bone

Branchial arches, or gill arches, are a series of bony "loops" present in fish, which support the gills. As gills are the primitive condition of vertebrates, all vertebrate embryos develop pharyngeal arches, though the eventual fate of these arches varies between taxa. In jawed fish, the first arch develops into the jaws, the second into the hyomandibular complex, with the posterior arches supporting gills. In amphibians and reptiles, many elements are lost including the gill arches, resulting in only the oral jaws and a hyoid apparatus remaining. In mammals and birds, the hyoid is still more simplified.

All basal vertebrates breathe with gills. The gills are carried right behind the head, bordering the posterior margins of a series of openings from the esophagus to the exterior. Each gill is supported by a cartilaginous or bony gill arch. Bony fish have four pairs of arches, cartilaginous fish have five to seven pairs, and primitive jawless fish have seven. The vertebrate ancestor no doubt had more arches, as some of their chordate relatives have more than 50 pairs of gills.Romer, A.S. (1949): ''The Vertebrate Body.'' W.B. Saunders, Philadelphia. (2nd ed. 1955; 3rd ed. 1962; 4th ed. 1970)

In amphibians and some primitive bony fish, the larvae bear external gills, branching off from the gill arches. These are reduced in adulthood, their function taken over by the gills proper in fish and by lungs in most amphibians. Some amphibians retain the external larval gills in adulthood, the complex internal gill system as seen in fish apparently being irrevocably lost very early in the evolution of tetrapods.Clack, J. A. (2002): Gaining ground: the origin and evolution of tetrapods. ''Indiana University Press'', Bloomington, Indiana. 369 pp

Function

The branchial system is typically used for respiration and/or feeding. Many fish have modified posterior gill arches into pharyngeal jaws, often equipped with specialized pharyngeal teeth for handling particular prey items (long, sharp teeth in carnivorous moray eels compared to broad, crushing teeth in durophagous black carp). In amphibians and reptiles, the hyoid arch is modified for similar reasons. It is often used in buccal pumping and often plays a role in tongue protrusion for prey capture. In species with highly specialized ballistic tongue movements such as chameleons or some plethodontid salamanders, the hyoid system is highly modified for this purpose, while it is often hypertrophied in species which use suction feeding. Species such as snakes and monitor lizards, whose tongue has evolved into a purely sensory organ, often have very reduced hyoid systems.

Components

The primitive arrangement is 7 (possibly 8) arches, each consisting of the same series of paired (left and right) elements. In order from dorsal-most to ventral-most, these elements are the pharyngobranchial, epibranchial, ceratobranchial, hypobranchial, and basibranchial. The pharyngobranchials may articulate with the neurocranium, while the left and right basibranchials connect to each other (often fusing into a single bone). When part of the hyoid system, the names of the bones are altered by replacing "-branchial" with "-hyal", thus "ceratobranchial" becomes "ceratohyal".

* The Basihyal and Basibranchials lie at the midline of the lower edge of the throat. Almost all modern chondrichthyans have a single midline basihyal, as do many teleosts, lungfish, and tetrapodomorphs. In tetrapods, the basihyal is known as the hyoid bone. Basibranchials, which are most common in osteichthyans, have the form of one or more rod-like bones projecting backwards along the throat.
* The Ceratohyals and Ceratobranchials lie above their respective basi- components, slanting backwards and upwards. They are often the largest bony components of the gill system, as well as the most essential and abundant components. Small connecting bones known as Hypophyals or Hypobranchials may link the basi- and cerato- components. Paired hypophyals are characteristic of living osteichthyans. Living chondrichthyans lack hypohyals, though several extinct forms are known to have had them.
* The Epihyals and Epibranchials lie above their respective cerato- components, slanting forwards, upwards, and often inwards. They are also essential components of the gill system, found in every fish. The epihyal is more commonly known as the hyomandibula, which is homologous to the stapes (sometimes known as the columnella) of tetrapods. In filter-feeding fish, the epibranchials often host gill rakers, specialized spines projecting backwards to trap plankton.
* The Pharhyngobranchials are the most dorsal bony elements of the gill system, connecting to the upper extent of the epibranchials. Living chondrichthyans have large pharyngobranchials which lean backwards and upwards. Osteichthyans, on the other hand, have two different types of pharyngobranchials: Suprapharyngobranchials are toothless structures similar to those of chondrichthyans, while Infrapharyngobranchials often possess teeth and lean inwards and forwards, forming the roof of the throat. A hyoid equivalent of the pharyngobranchial, the Pharyngohyal, is only found in living holocephalans, also known as chimaeras.

Amniotes

Amniotes do not have gills. The gill arches form as pharyngeal arches during embryogenesis, and lay the basis of essential structures such as jaws, the thyroid gland, the larynx, the ''columella'' (corresponding to the stapes in mammals) and in mammals the malleus and incus.

References

External links

The Gill Arches: Overview
'' Palaeos''. Retrieved 30 November 2014.

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Fish anatomy