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Mole salamander

(Redirected from Family Ambystomatidae)

The mole salamanders (genus Ambystoma) are a group of advanced salamanders endemic to North America. The group has become famous due to the presence of the axolotl (A. mexicanum), widely used in research due to its paedomorphosis, and the tiger salamander (A. tigrinum, A. mavortium) which is the official amphibian of many US states, and often sold as a pet.

Mole salamanders
Spotted salamander (Ambystoma maculatum)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Urodela
Family: Ambystomatidae
Genus: Ambystoma
Tschudi, 1838

General description

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Ambystoma kansensis (Adams 1929) fossil

Terrestrial mole salamanders are identified by having wide, protruding eyes, prominent costal grooves, and thick arms. Most have vivid patterning on dark backgrounds, with marks ranging from deep blue spots to large yellow bars depending on the species. Terrestrial adults spend most of their lives underground in burrows, either of their own making or abandoned by other animals. Some northern species may hibernate in these burrows throughout the winter. They live alone and feed on any available invertebrate. Adults spend little time in the water, only returning to the ponds of their birth to breed.

All mole salamanders are oviparous and lay large eggs in clumps in the water. Their fully aquatic larvae are branchiate, with three pairs of external gills behind their heads and above their gill slits. Larvae have large caudal fins, which extend from the back of their heads to their tails and to their cloacae. Larvae grow limbs soon after hatching, with four toes on the fore arms, and five toes on the hind legs. Their eyes are wide-set and lack true eyelids.

The larvae of some species (especially those in the south, and tiger salamanders) can reach their adult size before undergoing metamorphosis. During metamorphosis, the gills of the larvae disappear, as do the fins. Their tails, skin, and limbs become thicker, and the eyes develop lids. Their lungs become fully developed, allowing for a fully terrestrial existence.

Some species of mole salamanders (as well as populations of normally terrestrial species) are neotenic (retaining their larval form into adulthood). The most famous example is the axolotl. They cannot produce thyroxine, so their only means of metamorphosis is mainly through the outside injection of it. This usually shortens the lifespan of the salamander.

Tiger salamander complex

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Tiger salamander (Ambystoma tigrinum)

The presence of neotenic populations near those with large larvae has made it difficult to identify mole salamander species. The tiger salamander complex was previously considered a single species ranging from Canada to Mexico, falling under the name A. tigrinum. Despite differences in coloration and larvae, tiger salamanders were found throughout their unbroken range, which made it difficult to delineate subspecies, let alone elevate any populations to species status. In morphological terms, tiger salamanders are all very similar, with large heads, small eyes, and thick bodies. This is probably because tiger salamanders have the primitive morphology of mole salamanders. They are also the largest of the mole salamanders, and have very large larvae. All populations have similar lifestyles, and their lifecycles are identical. However, when one looks at tiger salamander populations distant from each other, different species within this complex become apparent. The ranges of these potential species overlap, and hybridization occurs, blurring the lines between species.

Several subspecies of A. tigrinum were named to deal with this problem. Recently, the barred tiger salamander (A. mavortium) was elevated to species status—covering the tiger salamander populations in the western and central United States. Several distinct subspecies still exist in A. mavortium, which may be elevated to species status at some point in the future. The California tiger salamander (A. californiense) has also been elevated out of A. tigrinum, and is actually very distantly related to all other mole salamander species. The Plateau tiger salamander (A. velasci) was elevated out of A. tigrinum through genetic analysis in 1997. All accounts referring to the axolotl (A. mexicanum) as a close relative of A. tigrinum are now considered wrong, as they are now separated by both geography and many species between. Instead, it is A. velasci, which shares the axolotl's habitat, and is probably closely related to it. The Plateau tiger salamander was probably the parent of most of the neotenic species, which raises the possibility that A. velasci is paraphyletic, and may be broken up into more species in the future.

Hybrid all-female populations

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Unisexual (all-female) populations of ambystomatid salamanders are widely distributed across the Great Lakes region and northeastern North America. The females require sperm from a co‑occurring, related species to fertilize their eggs and initiate development. Usually[1] the eggs then discard the sperm genome and develop asexually (i.e., gynogenesis, with premeiotic doubling); however, they may incorporate the genome from the sperm into the resulting offspring.[2] Sperm incorporation commonly[1] takes the form of genome addition (resulting in ploidy elevation in the offspring), or genome replacement, wherein one of the maternal genomes is discarded. This unique mode of reproduction has been termed kleptogenesis by Bogart and colleagues.[2] This is in contrast to hybridogenesis, where the maternal genomes are passed hemiclonally and the paternal genome is discarded every generation before the egg matures and reacquired from the sperm of another species.

The nuclear DNA of the unisexuals generally comprises genomes from up to five species:[3] the blue-spotted salamander (A. laterale), Jefferson salamander (A. jeffersonianum), small-mouthed salamander (A. texanum), streamside salamander (A. barbouri), and tiger salamander (A. tigrinum), denoted respectively as L, J, Tx, B, and Ti. This flexibility results in a large number of possible nuclear biotypes (genome combinations) in the unisexuals. For example, an LJJ individual would be a triploid with one A. laterale genome and two A. jeffersonianum genomes, while an LTxJTi individual would be a tetraploid with genomes from four species. Because they have hybrid genomes, unisexual salamanders are a cryptic species with morphology similar to coexisting species. For example, LLJs look like blue-spotted salamanders and LJJs look like Jefferson salamanders. Silvery salamanders LJJ (A. platineum), Tremblay's salamanders LLJ (A. tremblayi), and Kelly's Island salamanders LTxTx and LTxTi (A. nothagenes) were initially described as species. Species names were later dropped for all unisexual salamanders because of the complexity of their genomes. The offspring of a single mother may have different genome complements;[2] for example, a single egg mass may have both LLJJ and LJJ larvae.

Despite the complexity of the nuclear genome, all unisexuals form a monophyletic group based on their mitochondrial DNA. The maternal ancestor of the unisexual ambystomatids was most closely related to the streamside salamander, with the original hybridization likely occurring 2.4~3.9 million years ago,[2] making it the oldest known lineage of all-female vertebrates.[4] The hybridization was most probably with an A. laterale. All known unisexuals have at least one A. laterale genome[3] and this is thought to be essential for unisexuality. However, the A. laterale genome has been replaced several times, independently, in each of the lineages by matings with A. laterale.

Limb regeneration

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Ambystoma mexicanum, a neotenic salamander with exceptional regenerative capabilities is one of the principal models for studying limb regeneration.[5] Limb regeneration involves the propagation of a mass of low differentiated and highly proliferative cells termed the blastema.[5][6] During limb regeneration, blastema cells experience DNA double-strand breaks and thus require homologous recombination, a form of DNA repair that deals with double-strand breaks.[6]

Taxonomy

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Phylogenetic tree showing relations among Ambystoma species and outgroups: For example, the sister taxon to Ambystoma macrodactylum is Ambystoma laterale, meaning they share a single common ancestor and are each other's closest living relatives.

Rhyacosiredon was previously considered a separate genus within the family Ambystomatidae. However, cladistic analysis of the mole salamanders found the existence of Rhyacosiredon makes Ambystoma paraphyletic, since the species are more closely related to some Ambystoma species than those species are to others in Ambystoma. The stream-type morphology of these salamanders (which includes larvae and neotenes with short gills and thicker gular folds) may have led to their misclassification as a different genus.

The genus name Ambystoma was given by Johann Jakob von Tschudi in 1839,[7] and is traditionally translated as "cup-mouth",[citation needed]. Tschudi did not provide a derivation for the name, and many thought that he intended the name Amblystoma, "blunt-mouth." Occasionally, old specimens and documents use the name Amblystoma. Writing in 1907, Leonhard Stejneger offered a derivation of Ambystoma based on the contraction of a Greek phrase meaning "to cram into the mouth,"[8][9] but others have not found this explanation convincing.[10] In the absence of clear evidence that Tschudi committed a lapsus, the name given in 1839 stands.

Species

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This genus contains 32 species, listed below, the newest being A. bishopi. Some Ambystoma species are Terrestrial, others are neotenic, and some species have established populations of both neotenic and terrestrial forms.

Image Species and author Common name Distribution Lifestyle IUCN status
  A. altamirani

Dugès, 1895

Mountain stream salamander, Achoque Central Mexico, west and south of the Valley of Mexico Terrestrial and neotenic  
A. amblycephalum

Taylor, 1940

Blunt-headed salamander West-central Mexico (Michoacán state), near Morelia Terrestrial and neotenic  
  A. andersoni

(Brandon and Krebs, 1984)

Anderson's salamander West-central Mexico (Michoacán state), Laguna de Zacapu Neotenic  
  A. annulatum

Cope, 1886

Ringed salamander South-central United States (Arkansas, Illinois, Missouri, Oklahoma), Ozark Plateau and Ouachita Mountains Terrestrial  
  A. barbouri

Kraus & Petranka, 1989

Streamside salamander South-midwest United States (Indiana, Kentucky, Ohio, Tennessee, West Virginia) Terrestrial  
A. bishopi

Pauly, Piskurek & Shaffer, 2007

Reticulated flatwoods salamander Southeast United States (Florida Panhandle and southernmost Georgia), west of the Apalachicola-Flint River Terrestrial  
A. bombypellum

(Taylor, 1940)

Delicate-skinned salamander Central Mexico (State of Mexico) near Jilotepec Terrestrial  
  A. californiense

Gray, 1853

California tiger salamander Central Valley of California Terrestrial  
  A. cingulatum

Cope, 1868

Frosted flatwoods salamander Southeast United States (southern South Carolina and Georgia south to northern Florida) Terrestrial  
  A. dumerilii

(Dugès, 1870)

Lake Pátzcuaro salamander, Achoque West-central Mexico (Michoacán state), Lake Pátzcuaro Neotenic  
  A. flavipiperatum

Dixon, 1963

Yellow-peppered salamander, Ajolote de Chapala West-central Mexico (Jalisco) Terrestrial  
  A. gracile

(Baird, 1859)

Northwestern salamander Northwest North America (southernmost Alaska to northern California) Terrestrial  
A. granulosum

Taylor, 1944

Granular salamander, Ajolote Central Mexico (State of Mexico) near Toluca Terrestrial  
  A. jeffersonianum

(Green, 1827)

Jefferson salamander Northeastern North America (Ontario south to Virginia and west to Illinois) Terrestrial  
  A. laterale

Hallowell, 1856

Blue-spotted salamander Northeastern North America (Nova Scotia west to Manitoba and Minnesota and south to Indiana and New Jersey) Terrestrial  
  A. leorae

Taylor, 1943

Leora's stream salamander, Ajolote Central Mexico (Mexico state - Puebla border), Mount Tlaloc Terrestrial  
A. lermaense

(Taylor, 1940)

Lake Lerma salamander Central Mexico (State of Mexico), Lake Lerma near Toluca Terrestrial and neotenic  
  A. mabeei

Bishop, 1928

Mabee's salamander Coastal southeast United States (southeast Virginia to South Carolina) Terrestrial  
  A. macrodactylum

Baird, 1950

Long-toed salamander Northwest North America (Alaska south to northern California and east to Alberta and Montana) Terrestrial  
  A. maculatum

(Shaw, 1802)

Spotted salamander Eastern North America (Nova Scotia west to Wisconsin and south to eastern Texas and Georgia) Terrestrial  
  A. mavortium

Baird, 1850

Barred tiger salamander Western North America (Manitoba south to Texas and west to Washington and California) Terrestrial and neotenic  
  A. mexicanum

(Shaw and Nodder, 1798)

Axolotl Central Mexico (State of Mexico), Lake Xochimilco Neotenic  
  A. opacum

(Gravenhorst, 1807)

Marbled salamander Eastern United States (New Hampshire south to northern Florida and east to Missouri and Texas) Terrestrial  
A. ordinarium

Taylor, 1940

Puerto Hondo stream salamander West-central Mexico (Michoacán state), Puerto Hondo stream Terrestrial and neotenic  
  A. rivulare

Taylor, 1940

Michoacan stream salamander Central Mexico (western State of Mexico) Terrestrial and neotenic  
  A. rosaceum

Taylor, 1941

Tarahumara salamander Northwest Mexico, Sierra Madre Occidental Terrestrial and neotenic  
A. silvense

Webb, 2004

Durango salamander Northwest Mexico (Durango and Chihuahua), Sierra Madre Occidental Terrestrial and neotenic  
  A. talpoideum

Holbrook, 1838

Mole salamander Southeast United States (Virginia west to Oklahoma and south to northern Florida) Terrestrial and neotenic  
  A. taylori

Brandon, Maruska, and Rumph, 1982

Taylor's salamander Southeast Mexico (Puebla), Laguna Alchichica Neotenic  
  A. texanum

Matthes, 1855

Small-mouth salamander South-central United States (Ohio west to Nebraska and south to Texas and Alabama) Terrestrial  
  A. tigrinum

(Green, 1825)

Eastern tiger salamander Eastern North America (New York northwest to Manitoba and south to Texas and northern Florida) Terrestrial and neotenic  
  A. velasci

(Dugès, 1888)

Plateau tiger salamander Mexican Plateau Terrestrial and neotenic  

In addition, two groups of unisexual hybrid populations are sometimes named under their own species:

See also

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References

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  1. ^ a b Bi, Ke; Bogart, James P.; Fu, Jinzhong (2008). "The prevalence of genome replacement in unisexual salamanders of the genus Ambystoma (Amphibia, Caudata) revealed by nuclear gene genealogy". BMC Evolutionary Biology. 8 (1): 158. Bibcode:2008BMCEE...8..158B. doi:10.1186/1471-2148-8-158. ISSN 1471-2148. PMC 2413238. PMID 18498635.
  2. ^ a b c d Bogart, James P.; Bi, Ke; Jinzong Fu; Noble, Daniel W.A.; Niedzwiecki, John (February 2007). "Unisexual salamanders (genus Ambystoma) present a new reproductive mode for eukaryotes". Genome. 50 (2): 119–136. doi:10.1139/g06-152. ISSN 0831-2796. PMID 17546077.
  3. ^ a b Bogart, J.P.; Bartoszek, J.; Noble, D.W.A.; Bi, K. (29 July 2009). "Sex in unisexual salamanders: discovery of a new sperm donor with ancient affinities". Heredity. 103 (6): 483–493. doi:10.1038/hdy.2009.83. ISSN 0018-067X. PMID 19639004.
  4. ^ Bi, Ke; Bogart, James P. (2010). "Time and time again: Unisexual salamanders (genus Ambystoma) are the oldest unisexual vertebrates". BMC Evolutionary Biology. 10 (1): 238. Bibcode:2010BMCEE..10..238B. doi:10.1186/1471-2148-10-238. ISSN 1471-2148. PMC 3020632. PMID 20682056.
  5. ^ a b García-Lepe UO, Cruz-Ramírez A, Bermúdez-Cruz RM. DNA repair during regeneration in Ambystoma mexicanum. Dev Dyn. 2021 Jun;250(6):788-799. doi: 10.1002/dvdy.276. Epub 2020 Dec 17. PMID 33295131
  6. ^ a b García-Lepe UO, Torres-Dimas E, Espinal-Centeno A, Cruz-Ramírez A, Bermúdez-Cruz RM. Evidence of requirement for homologous-mediated DNA repair during Ambystoma mexicanum limb regeneration. Dev Dyn. 2022 Jun;251(6):1035-1053. doi: 10.1002/dvdy.455. Epub 2022 Jan 25. PMID 35040539
  7. ^ Tschudi, Johann Jakob (1839). "Classification der Batrachier, mit Berucksichtigung der Fossilen Thiere dieser Abtheilung der Reptilien". Mémoires de la Société des Sciences Naturelles de Neuchatel. 2 (4): 57, 92.
  8. ^ Stejneger, Leonhard (1907). "Herpetology of Japan and Adjacent Territory". Bulletin of the United States National Museum. 58: 24. hdl:2027/mdp.39015006820313.
  9. ^ Lyon Jr., M. W. (30 June 1916). "Ambystoma not Amblystoma". Science. 43 (1122): 929–930. doi:10.1126/science.43.1122.929-a. JSTOR 1639383. PMID 17793100.
  10. ^ Scott, Charles P. G. (1 September 1916). "Amblystoma not Ambystoma". Science. 44 (1131): 309–311. doi:10.1126/science.44.1131.309-a. JSTOR 1642899. PMID 17840073. S2CID 5490505.
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