Parietal eye

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The parietal eye (very small grey oval between the regular eyes) of a juvenile bullfrog (Lithobates catesbeianus) Frog parietal eye.JPG
The parietal eye (very small grey oval between the regular eyes) of a juvenile bullfrog ( Lithobates catesbeianus )
Adult green anole (Anolis carolinensis) clearly showing the parietal eye (small grey/clear oval) at the top of its head Anolis carolinensis parietal eye.JPG
Adult green anole (Anolis carolinensis) clearly showing the parietal eye (small grey/clear oval) at the top of its head
Parietal eye of the Merrem's Madagascar swift (Oplurus cyclurus) is surrounded by a black-and-white spot on the skin, giving it the "three-eyed" appearance Madagascar spiny tailed iguana cropped.jpg
Parietal eye of the Merrem's Madagascar swift ( Oplurus cyclurus ) is surrounded by a black-and-white spot on the skin, giving it the "three-eyed" appearance

A parietal eye (third eye, pineal eye) is a part of the epithalamus in some vertebrates. The eye is at the top of the head; is photoreceptive; and is associated with the pineal gland, which regulates circadian rhythmicity and hormone production for thermoregulation. [1] The hole that contains the eye is known as the pineal foramen or parietal foramen, because it is often enclosed by the parietal bones.

Contents

The parietal eye was discovered by Franz Leydig, in 1872, from work with lizards. [2]

Discovery

Franz Leydig, a professor of zoology at the University of Tübingen, dissected four species of European lizards—the slow worm ( Anguis fragilis ) and three species of Lacerta . [2] in 1872; [3] He found cup-like protrusions under the middles of their brains. He believed the protrusions to be glandular and called them frontal organs (German Stirnorgan). [2]

In 1886, Walter Baldwin Spencer, an anatomist at the University of Oxford, reported the results of his dissection of 29 species of lizards; he noted the presence of the same structure that Leydig had described. Spencer called it the pineal eye or parietal eye and noticed that it was associated with the parietal foramen and the pineal stalk. [4] In 1918, Nils Holmgren, a Swedish zoologist, found the pineal eye in frogs and dogfish. [5] He noted that the structure contained sensory cells that looked like the cone cells of the retina, [6] and hypothesised that the pineal eye could be a primitive light-sensing organ (photoreceptor). The organ has become popularly known as the "third eye". [5]

Presence in various animals

The parietal eye is found in the tuatara, most lizards, frogs, salamanders, certain bony fish, sharks, and lampreys. [7] [8] [9] It is absent in mammals but was present in their closest extinct relatives, the therapsids, suggesting that it was lost during the course of the mammalian evolution due to it being useless in endothermic animals. [10] It is also absent in the ancestrally endothermic ("warm-blooded") archosaurs such as birds. The parietal eye is also lost in ectothermic ("cold-blooded") archosaurs like crocodilians, and in turtles, which may be grouped with archosaurs in Archelosauria. [11] Despite being lepidosaurs, as lizards and tuatara are, snakes lack a parietal eye. [12] [13]

Anatomy

The third eye is much smaller than the main paired eyes; in living species, it is always covered by skin, and is usually not readily visible externally. [14] The parietal eye is a part of the epithalamus, which can be divided into two major parts—the epiphysis (the pineal organ; or the pineal gland, if it is mostly endocrine) and the parapineal organ (often called the parietal eye or, if it is photoreceptive, the third eye). The structures arise as a single anterior evagination of the pineal organ or as a separate outgrowth of the roof of the diencephalon; during development, it divides into two bilaterally somewhat symmetric organs, which rotate their location to become a caudal pineal organ and a parapineal organ. In some species, the parietal eye protrudes through the skull. [15] [16] The parietal eye's way [ further explanation needed ] of detecting light differs from the use of rod cells and cone cells in a normal vertebrate eye. [17]

Many of the oldest fossil vertebrates, including ostracoderms, placoderms, crossopterygians, and early tetrapods, have in their skulls sockets that appear to have held functional third eyes. The socket remains as a foramen between the parietal bones in many living amphibians and reptiles, although it has vanished in birds and mammals.

Lampreys have two parietal eyes, one that developed from the parapineal organ and the other from the pineal organ. These are one behind the other in the centre of the upper surface of the braincase. Because lampreys are among the most primitive of all living vertebrates, it is possible that was the original condition among vertebrates, and may have allowed bottom-dwelling species to sense threats from above. [14] Saniwa , an extinct varanid lizard, probably had two parietal eyes, one that developed from the pineal organ and the other from the parapineal organ. Saniwa is the only known jawed vertebrate to have both a pineal and a parapineal eye. In most vertebrates, the pineal organ forms the parietal eye, however, in lepidosaurs it is formed from the parapineal organ, which suggests that Saniwa re-evolved the pineal eye. [18]

Comparative anatomy

The parietal eye of amphibians and reptiles appears relatively far forward in the skull; thus it may be surprising that the human pineal gland appears far away from this position, tucked away between the corpus callosum and cerebellum. Also the parietal bones, in humans, make up a portion of the rear of the skull, far from the eyes. To understand further, note that the parietal bones formed a part of the skull lying between the eyes in sarcopterygians and basal amphibians, but have moved further back in higher vertebrates. [19] Likewise in the brain of the frog, the diencephalon, from which the pineal stalk arises, appears relatively further forward, as the cerebral hemispheres are smaller but the optic lobes are far more prominent than the human mesencephalon, which is part of the brain stem. [20] In humans the optic tract, commissure, and optic nerve bridge the substantial distance between eyes and diencephalon. Likewise the pineal stalk of Petromyzon elongates very considerably during metamorphosis. [21]

Analogs in other species

Crustaceans at the nauplius stage (first-stage larva) have a single eye atop the head. The eye has a lens and senses the direction of light but can not resolve details. More sophisticated segmented eyes develop later on the sides of their heads, but the initial eye also stays for some time. Thus it is possible to say that, at some stage of development, crustaceans also have a "third eye". Some species, like the brine shrimp, retain the primary eye throughout all stages of their life. Most arthropods have one or more simple eyes, called ocelli, between their main, compound eyes. [22]

See also

Related Research Articles

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<span class="mw-page-title-main">Pineal gland</span> Endocrine gland in the brain of most vertebrates

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<span class="mw-page-title-main">Parietal bone</span> Bone in the human skull which, when joined together, forms the sides and roof of the cranium

The parietal bones are two bones in the skull which, when joined at a fibrous joint known as a cranial suture, form the sides and roof of the neurocranium. In humans, each bone is roughly quadrilateral in form, and has two surfaces, four borders, and four angles. It is named from the Latin paries (-ietis), wall.

<span class="mw-page-title-main">Fish anatomy</span> Study of the form or morphology of fishes

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<span class="mw-page-title-main">Pinealocyte</span> Main cells contained in the pineal gland

Pinealocytes are the main cells contained in the pineal gland, located behind the third ventricle and between the two hemispheres of the brain. The primary function of the pinealocytes is the secretion of the hormone melatonin, important in the regulation of circadian rhythms. In humans, the suprachiasmatic nucleus of the hypothalamus communicates the message of darkness to the pinealocytes, and as a result, controls the day and night cycle. It has been suggested that pinealocytes are derived from photoreceptor cells. Research has also shown the decline in the number of pinealocytes by way of apoptosis as the age of the organism increases. There are two different types of pinealocytes, type I and type II, which have been classified based on certain properties including shape, presence or absence of infolding of the nuclear envelope, and composition of the cytoplasm.

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

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<span class="mw-page-title-main">Robert C. Stebbins</span> American herpetologist

Robert Cyril Stebbins was an American herpetologist and illustrator known for his field guides and popular books as well as his studies of reptiles and amphibians. His Field Guide to Western Reptiles and Amphibians, first published in 1966, is still considered the definitive reference of its kind, owing to both the quality of the illustrations and the comprehensiveness of the text. A professor of zoology at the University of California, Berkeley, for over 30 years, he was the first curator of herpetology at the Museum of Vertebrate Zoology, a 1949 Guggenheim fellow, and author of over 70 scientific articles. His discovery of the ring species phenomenon in Ensatina salamanders is now a textbook example of speciation, and he performed extensive research on the parietal eye of reptiles. He produced nature films, supported science education in primary grades, and organized conservation efforts that aided in the passing of the 1994 California Desert Protection Act. After retirement he continued to paint, collect field notes, and write books. Stebbins is commemorated in the scientific names of three species: Batrachoseps stebbinsi, the Tehachapi slender salamander; Anniella stebbinsi, a legless lizard; and Ambystoma tigrinum stebbinsi, the endangered Sonora tiger salamander.

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<i>Thliptosaurus</i> Extinct genus of dicynodonts

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The postfrontal is a paired cranial bone found in many tetrapods. It occupies an area of the skull roof between and behind the orbits, lateral to the frontal and parietal bones, and anterior to the postorbital bone.

References

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