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Article 0015 Hybrid Ambystomids

Introduction


In the wild, unisexual hybrids occur throughout the Great Lakes region to New England and the Maritime Provinces of Canada (Petranka, 122). In this region, forms are typically polyploid chromosomes), female, and can consist of varying combinations of genetic material from A. laterale, A. jeffersonianum, A. texanun, and A. tigrinum. Most hybrid combinations are triploid, however, tetraploid and pentaploid individuals occasionally occur in some populations (Bogart, 1989; Bogard and Licht 1986; Kraus 1985). Diploid unisexual individuals possessing genomes from A. laterale and A. texanum are common in northwestern Ohio and southeastern Michigan (Petranka, 122).     

Some unisexual biotypes have been given names, A. nothagenes, A. platineum, and A. tremblayi. However, most hybrids are referred to by their genomic compliments (see following).   

J  - A. jeffersonianum

L  - A. laterale

T  - A. texanum

Ti - A. tigrinum

These initials are used to describe the ploidy of a given hybrid. For example, "JLL" describes a hybrid with one set of genes from A. jeffersonianum, and two sets of genes from A. laterale. Positively identified combinations include: JL, LT, JJL, JLL, JLT, JLTi, LLT, LTT, LTTi, TTT, JJLT, JLLL, LLLL, LLLT, LLTT, LTTT, LTTi, and JLLLL (Bogart and Licht 1986; Bogart et al. 1985, 1987; Downs 1978; Kraus et al. 1991; Licht and Bogart 1987, 1989; Lowcock and murphy 1991; Lowcock eta al. 1991, 1992; Morris and Brandon 1984; Uzzel 1964).   

The "Ambystoma jeffersonianum Complex" consists of the two bisexual diploid species A. jeffersonianum (JJ), A. laterale (LL), and two unisexual triploids, A. platineum (JJL) and A. tremblayi (JLL). JJL and JLL are unisexual females, as genetic material from the male only stimulates egg development (however, there are rare cases of male hybrids). It is though that the "Ambystoma jeffersonianum Complex" arose as a result of one ore more hybridizations between JJ and LL, followed by 'backcrossing' with the diploid parents, which resulted in unisexual triploids. Unisexuals produce unreduced ova that are stimulated to divide when a sperm of a diploid male penetrates the egg membrane. In other words, fertilization does not ensue, so the males genes do not contribute to the resulting embryo (Petranka, 123). This would mean that unisexuals are sexually dependent upon bisexual diploids (Macgregor and Uzzell, 1964). A. jeffersnonianum males breed with A. platineum females, and A. laterale males breed with A. tremblayi females (Behler 291-292). JJL and JLL have larger cells and nuclei, larger eggs, and smaller clutches than JJ and LL.  

Morris and Brandon (1984) documented the unisexual polyploid JJLT in Illinois.  JLT and JLTi unisexuals have been found on Kelly's Island in Lake Erie (Kraus, 1985). Specimens from Kelly's Island, A. nothagenes, have been documented as being diploid, triploid, and tetraploid types with A. laterale, A. texanum, and A. tigrinum genomes.

References

Bogart, J. P. 1989. A mechanism for interspecific gene exchange via all-female salamander hybrids. New York State Museum Bulletin 466: 170-179.

Bogart, J. P., and L. E. Licht. 1986. Reproduction and the origin of polyploids in hybrid salamanders of the genus Ambystoma. Canadian Journal of Genetics and Cytology 60: 848-855.

Downs, F. L. 1978. Unisexual Ambystoma from the Bass Islands of Lake Erie. Occasional Papers of the Museum of Zoology, University of Michigan 685: 1-36.

Kraus, F. 1988. An empirical evaluation of the use of the ontogeny polarization criterion in phylogenetic inference. Systematic Zoology 37: 106-141.

Kraus, F. 1985. Unisexual salamander lineages in northwestern Ohio and southeastern Michigan: A study of the Consequences of Hybridization. Copeia 1985: 309-324.

Kraus, F., and James Petranka. 1989. A new sibling species of Ambystoma from the Ohio River drainage. Copeia 1989: 94-110.

Kraus, F., P.K Ducey, P. Moler, and M. M. Miyamoto. 1991. Two new triparental unisexual Ambystoma from Ohio and Michigan. Herpetologica 47: 429-439.

Larson, Allan. 1984. Neontological inferences of evolutionary pattern and process in the salamander family Plethodontidae. Evolutionary Biology 17: 119-217.

Larson, Allan. 1991. A molecular perspective on the evolutionary relationships of the salamander families. Evolutionary Biology 25: 211-277.

Larson, A., and W. W. Dimmick. 1993. Phylogenetic relationships of the salamander families: A analysis of congruence among morphological and molecular characters. Herpetological Monographs 7: 77-93.

Larson, A., D. B. Wake, L. R. Maxson and R. Highton. 1981. A molecular phylogenetic perspective on the origins of morphological novelties in the salamanders of the tribe Plethodontini (Amphibia, Plethodontidae). Evolution 35: 405-422.

Licht, L. E., and J. P. Bogart. 1987. Ploidy and developmental rate in the salamander hybrid complex (genus Ambystoma). Evolution 41: 918-920.

Lowcock, L. A. 1994. Biotype, genomotype, and genotype: variable effects of polyploidy and hybridity on ecological partitioning in a bisexual-unisexual community of salamanders. Canadian Journal of Zoology 72: 104-117.

Lowcock, L. A., and R. W. Murphy. 1991. Pentaploidy in hybrid salamanders demonstrates enhanced tolerance of multiple chromosome sets. Experientia 47: 490-493.

Lowcock, L. A., H. Griffith, and R. W. Murphy. 1991. The Ambystoma laterale-jeffersonianum complex in central Ontario: ploidy structure, sex ration and breeding dynamics in bisexual-unisexual communities. Copeia 1991: 87-105.

Morris, M. A., and R. A. Brandon. 1984. Gynogenesis and hybridization between Ambystoma platineum and Ambystoma texanum in Illinois. Copeia 1984: 324-337.

Petranka, James W. Salamanders of the United States and Canada. Smithsonian Institution Press, 1998.

Uzzel, T. M., Jr. 1964. Relations of the diploid and triploid species of the Ambystoma jeffersonianum complex (Amphibia, Caudata). Copeia 1964: 257-300.
 

 

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