Typhlonectes compressicauda

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Typhlonectes compressicauda
Typhlonectes compressicauda 2.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Gymnophiona
Clade: Apoda
Family: Typhlonectidae
Genus: Typhlonectes
Species:
T. compressicauda
Binomial name
Typhlonectes compressicauda
(Duméril & Bibron, 1841)
Typhlonectes compressicauda Map.jpg
Synonyms

Typhlonectes cunhaiCascon, Lima-Verde, and Benevides Marques, 1991

Contents

Typhlonectes compressicauda, the Cayenne caecilian, is a species of amphibian in the family Typhlonectidae that lives in water. It is found in Amazonian Brazil, Peru, and Colombia as well as in Guyana and French Guiana, and likely Suriname, [2] and according to some sources, Venezuela. [1] It is an aquatic caecilian that inhabits permanent rivers and marshes mainly in the lowland forest zone. [1]

Description

The Cayenne caecilian is an elongated, dark grey, black or steely blue amphibian with no limbs. The body is flattened laterally and has a number of transverse folds, giving it a segmented appearance. A long fin runs along its back, and it grows to a length of 30 to 55 cm (12 to 22 in).[ citation needed ] It has a more highly derived morphology than some more primitive species, showing differences in lung structure, the reproductive organs, and the kidneys. [3]

Distribution

The Cayenne caecilian occurs in South America, including the Amazon basin and river systems in the Guianas. It is found at altitudes of up to 200 m (660 ft) above sea level. Because it is common and has a wide range, it is listed as of "Least Concern" in the IUCN Red List of Threatened Species. [1]

Biology

The Cayenne caecilian lives in shallow streams and rivers. It spends the day in a communal burrow, emerging at night to hunt through the sediment for small invertebrates, such as insect larvae and shrimps. It also eats small fish. It has no functional eyes and probably detects its prey by touch or by the vibrations made when the prey moves. It has slime glands all over its body and secretes copious amounts of noxious mucous if attacked. Nevertheless, it is eaten by birds, snakes, and large fish.[ citation needed ]

At breeding time, a male and female Cayenne caecilian twine around each other and the male places a spermatophore in the female's cloaca. Fertilisation is internal and the Cayenne caecilian is ovoviviparous. Six to fourteen young hatch inside the female's oviduct with gills. At first, they feed on the yolks of their eggs, but they develop rasping teeth and later consume glandular secretions produced by the lining of the oviduct. Birth takes place after about eight months and the juvenile caecilians shed their temporary teeth and develop their adult dentition.[ citation needed ]

The Cayenne caecilian is considered to have several characteristics that are more highly derived than other more primitive species. Its karyotype has been compared with that of other caecilians, and its diploid number has been found to be 28, a fact that does not support the hypothesis that, during the period of amphibian evolution, the number of chromosomes became reduced. However, many caecilians have not yet been karyotyped and the exact evolutionary relationships between the species have not yet been determined, so the hypothesis is not necessarily incorrect. [3]

Typhlonectes compressicauda was included in a study of the evolutionary origin of acoustic communication. [4]

Related Research Articles

<span class="mw-page-title-main">Amphibian</span> Class of ectothermic tetrapods

Amphibians are ectothermic, anamniotic, four-limbed vertebrate animals that constitute the class Amphibia. In its broadest sense, it is a paraphyletic group encompassing all tetrapods, excluding the amniotes. All extant (living) amphibians belong to the monophyletic subclass Lissamphibia, with three living orders: Anura (frogs), Urodela (salamanders), and Gymnophiona (caecilians). Evolved to be mostly semiaquatic, amphibians have adapted to inhabit a wide variety of habitats, with most species living in freshwater, wetland or terrestrial ecosystems. Their life cycle typically starts out as aquatic larvae with gills known as tadpoles, but some species have developed behavioural adaptations to bypass this.

<span class="mw-page-title-main">Karyotype</span> Photographic display of total chromosome complement in a cell

A karyotype is the general appearance of the complete set of chromosomes in the cells of a species or in an individual organism, mainly including their sizes, numbers, and shapes. Karyotyping is the process by which a karyotype is discerned by determining the chromosome complement of an individual, including the number of chromosomes and any abnormalities.

<span class="mw-page-title-main">Lissamphibia</span> Subclass of amphibians

The Lissamphibia is a group of tetrapods that includes all modern amphibians. Lissamphibians consist of three living groups: the Salientia, the Caudata, and the Gymnophiona.

<span class="mw-page-title-main">Caecilian</span> Order of amphibians

Caecilians are a group of limbless, vermiform (worm-shaped) or serpentine (snake-shaped) amphibians with small or sometimes nonexistent eyes. They mostly live hidden in soil or in streambeds, and this cryptic lifestyle renders caecilians among the least familiar amphibians. Modern caecilians live in the tropics of South and Central America, Africa, and southern Asia. Caecilians feed on small subterranean creatures such as earthworms. The body is cylindrical and often darkly coloured, and the skull is bullet-shaped and strongly built. Caecilian heads have several unique adaptations, including fused cranial and jaw bones, a two-part system of jaw muscles, and a chemosensory tentacle in front of the eye. The skin is slimy and bears ringlike markings or grooves and may contain scales.

<span class="mw-page-title-main">Lepospondyli</span> Polyphyletic group of tetrapodomorphs

Lepospondyli is a diverse taxon of early tetrapods. With the exception of one late-surviving lepospondyl from the Late Permian of Morocco, lepospondyls lived from the Early Carboniferous (Mississippian) to the Early Permian and were geographically restricted to what is now Europe and North America. Five major groups of lepospondyls are known: Adelospondyli; Aïstopoda; Lysorophia; Microsauria; and Nectridea. Lepospondyls have a diverse range of body forms and include species with newt-like, eel- or snake-like, and lizard-like forms. Various species were aquatic, semiaquatic, or terrestrial. None were large, and they are assumed to have lived in specialized ecological niches not taken by the more numerous temnospondyl amphibians that coexisted with them in the Paleozoic. Lepospondyli was named in 1888 by Karl Alfred von Zittel, who coined the name to include some tetrapods from the Paleozoic that shared some specific characteristics in the notochord and teeth. Lepospondyls have sometimes been considered to be either related or ancestral to modern amphibians or to Amniota. It has been suggested that the grouping is polyphyletic, with aïstopods being primitive stem-tetrapods, while recumbirostran microsaurs are primitive reptiles.

<i>Boulengerula taitana</i> Species of amphibian

Boulengerula taitana is a species of caecilian. It is endemic to the Taita Hills region of southeast Kenya. Boulengerula taitana are unique caecilians in appearance, fertilization type, and parental care. From their similar shape and presentation to worms, and their internalized fertilization, they set themselves apart from many other amphibians. D. taitana interactions between mothers and newly hatched young is unique in that the mother uses her own skin as a food resource for offspring. This species also has physiological adaptations in place to increase oxygen uptake and affinity to fit their underground lifestyle. The Boulengerula taitana differentiates itself from its close relatives in ways rarely documented and researched before.

<i>Boulengerula niedeni</i> Species of amphibian

Boulengerula niedeni, the Sagalla caecilian, is a worm-like amphibian first described in 2005. The species was described from a specimen discovered on Sagala Hill, an isolated mountain block of the Taita Hills in Kenya, and is not known from other areas.

<i>Atretochoana</i> Genus of amphibians

Atretochoana eiselti is a species of caecilian originally known only from two preserved specimens discovered by Sir Graham Hales in the Brazilian rainforest, while on an expedition with Sir Brian Doll in the late 1800s, but rediscovered in 2011 by engineers working on a hydroelectric dam project in Brazil. Until 1998, it was known only from the type specimen in the Naturhistorisches Museum, Vienna. Originally placed in the genus Typhlonectes in 1968, it was reclassified into its own monotypic genus, Atretochoana, in 1996. It was also found to be more closely related to the genus Potamotyphlus than Typholonectes. The species is the largest of the few known lungless tetrapods, and the only known lungless caecilian.

<i>Chthonerpeton indistinctum</i> Species of amphibian

Chthonerpeton indistinctum is a species of caecilian in the family Typhlonectidae. It is found in northeastern Argentina, Paraguay, Uruguay, and southeastern Brazil. The common name Argentine caecilian has been coined for it.

<i>Dermophis mexicanus</i> Species of amphibian

Dermophis mexicanus, also known commonly as the Mexican burrowing caecilian or the Mexican caecilian, and locally as the tapalcua or tepelcua, is a species of limbless amphibian in the family Dermophiidae. The species is native to Mexico and Central America, where it burrows under leaf litter and plant debris.

Oscaecilia zweifeli is a species of caecilian in the family Caeciliidae. It is a poorly known species only known from few specimens: the holotype from the imprecise type locality, "a small creek tributary to Río Mazaruni" in Guyana, one from similarly imprecise Cayenne in French Guiana, and another one from the Nouragues research station in French Guiana. The specific name zweifeli honors Richard G. Zweifel, an American herpetologist. Common names Zweifel's caecilian and tributary caecilian have been coined for it.

<i>Siphonops annulatus</i> Species of amphibian

Siphonops annulatus, the ringed caecilian, is a species of caecilian in the family Siphonopidae from South America. It might have the broadest known distribution among terrestrial caecilian species.

<i>Typhlonectes natans</i> Species of amphibian

Typhlonectes natans, also incorrectly called the rubber eel, is a species of caecilian in the family Typhlonectidae found in Colombia, Venezuela, and possibly Trinidad and Tobago. Its natural habitats are dry savanna, subtropical or tropical dry shrubland, subtropical or tropical moist shrubland, subtropical or tropical seasonally wet or flooded lowland grassland, and rivers. T. natans is commonly kept as an aquarium pet, and is sometimes sold as a "fish" in aquarium stores.

<i>Ichthyophis glutinosus</i> Species of amphibian

Ichthyophis glutinosus, the Ceylon caecilian or common yellow-banded caecilian, is a species of caecilian in the family Ichthyophiidae endemic to Sri Lanka. Its natural habitats are moist tropical and subtropical forests and pastures.

<span class="mw-page-title-main">Koh Tao Island caecilian</span> Species of amphibian

The Koh Tao Island caecilian is a species of amphibian in the family Ichthyophiidae found in Cambodia, Laos, Myanmar, Thailand, and Vietnam. Also known as the Ichthyophis bannanicus, the Banna caecilian, it is also found in southern China.

Rhinatrema nigrum, the black caecilian, is a species of caecilian in the family Rhinatrematidae found in Guyana, Venezuela, and possibly Brazil. Its natural habitats are subtropical or tropical moist lowland forests, subtropical or tropical moist montane forests, rivers, and intermittent rivers.

Rhinatrema is a genus of caecilians in the family Rhinatrematidae. Their common name is two-lined caecilians. The genus is known from the Guyanas and adjacent Brazil. Most Rhinatrema are known to inhabit and live in areas of tropical forests where there is an abundance of dense, dead vegetation matter.

<i>Gerobatrachus</i> Extinct genus of amphibians

Gerobatrachus is an extinct genus of amphibamid temnospondyl that lived in the Early Permian, approximately 290 million years ago (Ma), in the area that is now Baylor County, Texas. When it was first described in 2008, Gerobatrachus was announced to be the closest relative of Batrachia, the group that includes modern frogs and salamanders. It possesses a mixture of characteristics from both groups, including a large frog-like head and a salamander-like tail. These features have led to it being dubbed a frogamander by the press. Some more recent studies place Gerobatrachus as the closest relative of Lissamphibia, the group that contains all modern amphibians including frogs, salamanders, and caecilians, or place modern amphibians far from Gerobatrachus within a group called Lepospondyli.

<i>Rhynchonkos</i> Extinct genus of tetrapods

Rhynchonkos is an extinct genus of rhynchonkid microsaur. Originally known as Goniorhynchus, it was renamed in 1981 because the name had already been given to another genus; the family, likewise, was originally named Goniorhynchidae but renamed in 1988. The type and only known species is R. stovalli, found from the Early Permian Fairmont Shale in Cleveland County, Oklahoma. Rhynchonkos shares many similarities with Eocaecilia, an early caecilian from the Early Jurassic of Arizona. Similarities between Rhynchonkos and Eocaecilia have been taken as evidence that caecilians are descendants of microsaurs. However, such a relationship is no longer widely accepted.

<span class="mw-page-title-main">Salientia</span> Order of amphibians

The Salientia are a total group of amphibians that includes the order Anura, the frogs and toads, and various extinct proto-frogs that are more closely related to the frogs than they are to the Urodela, the salamanders and newts. The oldest fossil "proto-frog" appeared in the early Triassic of Madagascar, but molecular clock dating suggests their origins may extend further back to the Permian, 265 million years ago.

References

  1. 1 2 3 4 Enrique La Marca, Claudia Azevedo-Ramos, Marinus Hoogmoed, Mark Wilkinson, John Measey (2010). "Typhlonectes compressicauda". IUCN Red List of Threatened Species . 2010: e.T59599A11959503. doi: 10.2305/IUCN.UK.2010-2.RLTS.T59599A11959503.en . Retrieved 12 November 2021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. Frost, Darrel R. (2014). "Typhlonectes compressicauda (Duméril and Bibron, 1841)". Amphibian Species of the World: an Online Reference. Version 6.0. American Museum of Natural History. Retrieved 30 January 2015.
  3. 1 2 M.H. Wake; J.C. Hafner; M. S. Hafner; L.L. Klosterman; J. L. Patton (1980). "The karyotype of Typhlonectes compressicauda (Amphibia: Gymnophiona) with comments on chromosome evolution in caecilians" (PDF). Experientia. 36 (2): 171–172. doi:10.1007/bf01953713. PMID   7371747. S2CID   20808756.
  4. Jorgewich-Cohen, Gabriel; Townsend, Simon William; Padovese, Linilson Rodrigues; Klein, Nicole; Praschag, Peter; Ferrara, Camila R.; Ettmar, Stephan; Menezes, Sabrina; Varani, Arthur Pinatti; Serano, Jaren; Sánchez-Villagra, Marcelo R. (2022-10-25). "Common evolutionary origin of acoustic communication in choanate vertebrates". Nature Communications. 13 (1): 6089. doi:10.1038/s41467-022-33741-8. ISSN   2041-1723. PMC   9596459 . PMID   36284092.