Mitochondrial DNA variability in viviparous and ovoviviparous populations of the urodele Salamandra salamandra

Mitochondrial DNA analysis of 13 populations of S. salamandra along a transect across the North of the Iberian Peninsula showed values of divergence between haplotypes ranging from d = 0.41% to 5.91%. Phenetic and cladistic analysis grouped the isofemale lineages into two main clusters with contrast...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Dopazo, H.
Otros Autores: Boto, L., Alberch, P.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1998
Acceso en línea:Registro en Scopus
DOI
Handle
Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 09568caa a22008417a 4500
001 PAPER-3024
003 AR-BaUEN
005 20230518203230.0
008 190411s1998 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-0031921381 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JEBIE 
100 1 |a Dopazo, H. 
245 1 0 |a Mitochondrial DNA variability in viviparous and ovoviviparous populations of the urodele Salamandra salamandra 
260 |c 1998 
270 1 0 |m Dopazo, H.; Depto. Geologia, UBA. Pab. II, Cdad. Universitaria, 1428 Buenos Aires, Argentina; email: dopazo@tango.gl.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Alcobendas, M., Dopazo, H., Alberch, P., Geographic variation in allozymes of populations of Salamandra salamandra (Amphibia: Urodela) exhibiting distinct reproductive modes (1996) J. Evol. Biol., 9, pp. 83-102 
504 |a Avise, J.C., Arnold, J., Ball, R.M., Bermingham, E., Lamb, T., Neigel, J.E., Rebb, C.A., Saunders, N.C., Intraspecific phylogeography: The mitochondrial DNA bridge between population genetics and systematics (1987) Annu. Rev. Ecol. Syst., 18, pp. 489-522 
504 |a Bas, S., (1983) Estudio de La Situación Microevolutiva y de La Ecologia de La Salamandra Salamandra (L) en el N.OE. Iberico, , Thesis, Univ. Santiago. Spain 
504 |a Bas, S., Gasser, F., Polytypism of Salamandra salamandra (L.) in North-Western Iberia (1994) Mertensiella, 4, pp. 41-74 
504 |a Carr, S.M., Brothers, J.A., Wilson, A.C., Evolutionary inferences from restriction maps of mitochondrial DNA from nine taxa of Xenopus frogs (1987) Evolution, 41, pp. 176-188 
504 |a Cordonnier, A.M., Vannier, P.A., Brum, G.M., A restriction map of Xenopus laevis mitochrondrial DNA (1982) Eur. J. Bioch., 126, pp. 119-127 
504 |a Cracraft, J., The origin of evolutionary novelties: Pattern and process at different hierarchical levels (1990) Evolutionary Innovations, pp. 21-44. , Matthew H. Nitecki (Eds.), Univ. of Chicago Press, Chicago 
504 |a Debry, R.W., Slade, N.A., Cladistic analysis of restriction endonuclease cleavage maps within a maximum-likelihood framework (1985) Syst. Zool., 34, pp. 21-34 
504 |a Dopazo, H., (1995) Evolución Intraespecifica de Una Caracteristica Macroevolutiva: Viviparismo en Salamandra Salamandra, , PhD Thesis, Universidad Autónoma. Madrid. Spain 
504 |a Dopazo, H., Alberch, P., Preliminary results on optional viviparism and intrauterine siblicide in Salamandra salamandra populatins from Northern Spain (1994) Mertensiella, 4, pp. 7-23 
504 |a Dowling, T.E., Smith, G.R., Brown, W.M., Reproductive isolation and introgression between Notropis cornutus and Notropis chrysocephalus (family Cyprinidae): Comparison of morphology, allozymes, and mitochondrial DNA (1989) Evolution, 43, pp. 620-634 
504 |a Farris, J.S., Distances and statistics (1986) Cladistics, 2, pp. 144-157 
504 |a Felsenstein, J., Phylogenies from restriction sites: A maximum likelihood approach (1992) Evolution, 46, pp. 159-173 
504 |a Felsenstein, J., PHYLIP phylogeny inference package (version 3.5c) (1993) Cladistics, 5, pp. 164-166 
504 |a Gasser, F., Le polytypisme de 1 èspéce paléarctique Salamanddra salamandra (L.) (Amphibien Urodele). I. Proteines sériques et groupes sériques (1978) Arch. Zool. Exp. & Gen., 119, pp. 585-618 
504 |a Joly, J.M., Données écologiques sur la salamandre tachetée Salamandra salamandra (L.) (1968) Ann. Sci. Nat. Zool., 10, pp. 301-366 
504 |a Nei, M., (1987) Molecular Evolutionary Genetics, , Columbia Univ. Press, N. Y 
504 |a Neigel, J.E., Avise, J.C., Phylogenetic relationships of mitochondrial DNA under various demographic models of speciation (1986) Evolutionary Processes and Theory, pp. 515-534. , E. Nevo and S. Karlin (Eds), Academic Press, N. Y 
504 |a O'Farrell, P.H., Kutter, E., Nakanishi, M., A restriction map of the bacteriophage T4 genome (1980) Mol. Gen. Genet., 179, pp. 421-435 
504 |a Saitou, N., Nei, M., The neighbor-joining method: A new method for reconstructing phylogenetics trees (1987) Mol. Biol. Evol., 4, pp. 406-425 
504 |a Swofford, D.L., (1990) PAUP: Phylogenetic Analysis Using Parsimony (Version 3.0), , Illinois Natl. Hist. Surv., Champaign, IL 
504 |a Thiesmeier, B., Haker, K., Salamandra salamandra bernardezi Welterstorff, 1928 aus OviedoSpanien, nebst bemerkungen zur viviparie in der gattun Salamandra (1990) Salamandra, 26, pp. 140-154 
504 |a Thorn, R., Les salamandres d'europe, d'asie et d'afrique du nord (1968) Paul Lechevalier, 35. , Paris 
504 |a Wake, M.H., (1982) Diversity Within a Framework of Constraints. Amphibia Reproductive Modes. Environment Adaptation and Evolution, , D. Massakowski and G. Roth (Eds.). Gustav Fischer Stuttgart, N. Y 
504 |a Wake, M.H., Evolution of oviductal gestation in Amphibians (1993) Jour. Exp. Zool., 266, pp. 394-413 
504 |a Walles, G.P., Mitochondrial DNA insertion polymorphism and germ line heteroplasmy in the Trituras cristatus complex (1987) Heredity, 58, pp. 229-238 
504 |a Wallis, G.P., Artzen, J.W., Mitochondrial DNA variation in the crested newt superspecies: Limited cytoplasmic gene flow among species (1989) Evolution, 43, pp. 88-104 
504 |a Wolterstorff, W., Vollmolch-gebärende Feuer-salamander aus Oviedo (1928) Bl. Aquar. Terrar. Kde., 39, pp. 132-133 
504 |a Zink, R.M., Dittmann, D.L., Gene flow, refugia and evolution of geographic variation in the song sparrow (Melospiza melodia) (1993) Evolution, 47, pp. 717-729 
520 3 |a Mitochondrial DNA analysis of 13 populations of S. salamandra along a transect across the North of the Iberian Peninsula showed values of divergence between haplotypes ranging from d = 0.41% to 5.91%. Phenetic and cladistic analysis grouped the isofemale lineages into two main clusters with contrasting phylogeographic patterns. The first group encompasses populations located at each extreme of the Iberian Peninsula. Despite the large geographic distance separating these populations, they exhibit only a minor degree of divergence among haplotypes. In contrast, much higher diversification, in both number of distinct haplotypes, and overall genetic divergence, was observed in the second group of phylogenetically related populations. Surprisingly, this process of radiation and divergence in mtDNA haplotypes occurred in populations in close geographic proximity. All populations sampled in this group are located within a 300 km range, in the central part of our transect across the Northern edge of the Peninsula. Most populations in the central range of our transect exhibit viviparous reproduction-which is derived and highly unusual among urodeles. The genetic distances measured among Asturian (central portion of our transect), viviparous populations are higher than the distances measured between the two main taxonomic clusters. A viviparous population showing an unusual level of mtDNA heterogeneity is reported and the potential implications of this focus of localized variability are discussed. The dynamics of isofemale lineages among the two reproductive modes was further explored in combination with the previous allozyme data. Several nuclear markers suggest that major mtDNA divergences could be explained by long-term extrinsic barriers to gene flow. Isofemale lineages indicate a narrow secondary contact zone among populations with different reproductive patterns. The existence of viviparous and ovovivparous populations sharing a common haplotype suggests that reproductive transition in S. salamandra could have arisen in absence of genetic mtDNA differentiation. We finally outline a genetic model system where the acquisition of water independence from a primitively aquatic dependent amphibian life cycle can be analyzed from a microevolutionary perspective.  |l eng 
593 |a Depto. Geologla, UBA. Pab. II, Cdad. Universitaria, 1428 Buenos Aires, Argentina 
593 |a Dpto. Biodiversidad y Biol. E., Museo Nacional de Ciencias Naturales, J. Gutierrez Abascal 2, E-28006 Madrid, Spain 
593 |a Lab. de Sist. y Evol. Molecular, Museo Nacional de Ciencias Naturales, J. Gutierrez Abascal 2, E-28006 Madrid, Spain 
690 1 0 |a MITOCHONDRIAL DNA 
690 1 0 |a S. SALAMANDRA 
690 1 0 |a SECONDARY CONTACT ZONES 
690 1 0 |a URODELES 
690 1 0 |a VIVIPARISM 
690 1 0 |a GENETIC DIVERSITY 
690 1 0 |a MITOCHONDRIAL DNA 
690 1 0 |a OVOVIVIPARY 
690 1 0 |a URODELE 
690 1 0 |a VIVIPARY 
690 1 0 |a SPAIN 
690 1 0 |a SALAMANDRA SALAMANDRA 
700 1 |a Boto, L. 
700 1 |a Alberch, P. 
773 0 |d 1998  |g v. 11  |h pp. 365-378  |k n. 3  |p J. Evol. Biol.  |x 1010061X  |w (AR-BaUEN)CENRE-5565  |t Journal of Evolutionary Biology 
856 4 1 |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-0031921381&doi=10.1007%2fs000360050093&partnerID=40&md5=967d10775d6b03a9a8f13fdb17d72792  |y Registro en Scopus 
856 4 0 |u https://doi.org/10.1007/s000360050093  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_1010061X_v11_n3_p365_Dopazo  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1010061X_v11_n3_p365_Dopazo  |y Registro en la Biblioteca Digital 
961 |a paper_1010061X_v11_n3_p365_Dopazo  |b paper  |c PE 
962 |a info:eu-repo/semantics/article  |a info:ar-repo/semantics/artículo  |b info:eu-repo/semantics/publishedVersion 
963 |a VARI 
999 |c 63977