1991
DOI: 10.1051/gse:19910401
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Polytypic chromosomal variation in Triturus boscai (Urodela : Salamandridae)

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Cited by 4 publications
(5 citation statements)
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“…For example, Arntzen et al () found clear signs of asymmetric viability of reciprocal‐cross hybrids between Triturus cristatus (crested) and T. marmoratus (marbled) newts that likely resulted from an incompatibility between the crested X chromosome and marbled cytoplasm, as adult F1 hybrids resulting from marbled‐female versus crested‐male crosses consisted entirely of males. Herrero () reported the formation of sterile hybrids of L. boscai resulting from crosses between two groups of populations differentiated by C‐band chromosomal patterns. According to this author, the occurrence of sterile hybrids derived from abnormalities during meiosis.…”
Section: Discussionmentioning
confidence: 99%
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“…For example, Arntzen et al () found clear signs of asymmetric viability of reciprocal‐cross hybrids between Triturus cristatus (crested) and T. marmoratus (marbled) newts that likely resulted from an incompatibility between the crested X chromosome and marbled cytoplasm, as adult F1 hybrids resulting from marbled‐female versus crested‐male crosses consisted entirely of males. Herrero () reported the formation of sterile hybrids of L. boscai resulting from crosses between two groups of populations differentiated by C‐band chromosomal patterns. According to this author, the occurrence of sterile hybrids derived from abnormalities during meiosis.…”
Section: Discussionmentioning
confidence: 99%
“…According to this author, the occurrence of sterile hybrids derived from abnormalities during meiosis. Considering that all L. boscai populations studied by Herrero () belong to the LBSE lineage (Martínez‐Solano et al, ; Teixeira et al, ), evidence of this intraspecific post‐zygotic reproductive barrier is somewhat intriguing in light of the successful experimental hybridization between L. boscai and other closely related newts (Bucci‐Innocenti, Ragghianti, & Mancino, ). Whereas asymmetry in backcrosses and in the distribution of mtDNA lineages could be explained by the action of pre‐ and post‐zygotic mechanisms, further field studies on population sex ratios and common garden experiments comparing the survival of parental lineages, hybrids and backcrosses in both directions are required to test these alternative but not mutually exclusive hypotheses.…”
Section: Discussionmentioning
confidence: 99%
“…However, more sampling in (possible) transition zones and the study of nuclear genes and morphology seems required, prior to any new arrangement. The distinct clade found by Herrero (1991) also deserves further attention. Quoting Martínez-Solano et al (2006): "(…) new data from independent sources are needed to clarify the taxonomic status of these two divergent lineages, and morphological and molecular studies including data on variation in nuclear markers will be particularly helpful in this respect.…”
Section: Caudata or Urodelamentioning
confidence: 90%
“…As another plausible scenario, individuals might disperse but fail to reproduce or exhibit asymmetrical reproductive success in occupied areas due to sexual selection (Aragón et al, 2000;Gabor et al, 2000;Babik et al, 2003) or genetic barriers (e.g. Herrero, 1991). These alternative but not mutually exclusive hypotheses have yet to be empirically tested with further field and laboratory experiments, explicitly taking into account the historical, ecological and geographical contexts in which the processes are taking place, i.e.…”
Section: Nuclear Dna Phylogeography Of Lissotriton Boscaimentioning
confidence: 99%