scholarly journals Scale-dependent effects of terrestrial habitat on genetic variation in the great crested newt (Triturus cristatus)

2021 ◽  
Author(s):  
Karen Cox ◽  
Mathieu Denoël ◽  
Hans Van Calster ◽  
Jeroen Speybroeck ◽  
Sam Van de Poel ◽  
...  
1999 ◽  
Vol 68 (3) ◽  
pp. 181-203 ◽  
Author(s):  
J.W. Arntzen ◽  
Graham P. Wallis

Within the newt genus Triturus, the large-bodied species in the T. cristatus (crested newt) superspecies show an unusual degree of variation in relative trunk length as a result of among-taxon variation in interlimb vertebral count. Here we examine the systematic value of this feature as assessed by both exterior measurement (Wolterstorff Index) and direct radiographic count of rib-bearing vertebrae, with particular reference to a number of confounding factors (sex differences, hybridisation, geographic variation, allometry, preservation effects). Using our mtDNA haplotype data, which are largely concordant with geographic distribution of species, we find that direct count ofthe rib-bearing vertebrae performs more reliably (14% misclassification) than external measurement (31% misclassification) as a species identifier. We therefore recommend this feature as a taxonomic tool, although (like external measurement) it breaks down near hybrid zones. To account for the observed biogeographicalpattern and phenotype-genotype discrepancies, a scenario is presented that combines the movement of the contact zone between taxa with asymmetric hybridisation. This scenario applies to species interactions in eastern Yugoslavia and western France.


1982 ◽  
Vol 47 (2) ◽  
pp. 139-147 ◽  
Author(s):  
Malacarne Giorgio ◽  
Cristina Giacoma ◽  
Camillo Vellano ◽  
Valdo Mazzi

2007 ◽  
Vol 76 (4) ◽  
pp. 261-278 ◽  
Author(s):  
J.W. Arntzen ◽  
G. Espregueira Themudo ◽  
B. Wielstra

Newts of the genus Triturus (Amphibia, Caudata, Salamandridae) are distributed across Europe and adjacent Asia. In spite of its prominence as a model system for evolutionary research, the phylogeny of Triturus has remained incompletely solved. Our aim was to rectify this situation, to which we employed nuclear encoded proteins (40 loci) and mitochondrial DNA-sequence data (mtDNA, 642 bp of the ND4 gene). We sampled up to four populations per species covering large parts of their ranges. Allozyme and mtDNA data were analyzed separately with parsimony, distance, likelihood and Bayesian methods of phylogenetic inference. Existing knowledge on taxonomic relationships was confirmed, including the monophyly of the genus and the groups of crested newts (four species) and marbled newts (two species). The genetic coherence of species and subspecies was also confirmed, but not always with high statistical support (depending on taxon, characters under consideration, and method of inference). In spite of our efforts we did not obtain sufficient phylogenetic signal to prefer one out of twelve potential topologies representing crested newts relationships. We hypothesize that the lack of phylogenetic resolution reflects a hard polytomy and represents the (near)-simultaneous origin of crested newt species. Using a calibration point of 24 Ma (million years before present) for the most recent common ancestor of Triturus-species, the crested newt radiation event is dated at 7-6 Ma (scenario 1) or at 11-10 Ma (scenario 2), depending on the application of an allozyme versus mtDNA molecular clock. The first biogeographical scenario involves the spread of crested newts from the central Balkans into four compass directions. This scenario cannot be brought into line with potential vicariance events for south-eastern Europe. The second scenario involves the more or less simultaneous origin of four species of crested newts through large-scale vicariance events and is supported by the paleogeographical reconstruction for the region at the end of the Middle Miocene. The subspecies Triturus carnifex macedonicus carries in one large area the mtDNA that is typical for the neighbouring species T. karelinii, which is attributed to introgression and a recent range shift. It is nevertheless a long distinct evolutionary lineage and we propose to elevate its taxonomic status to that of a species, i.e., from Triturus c. macedonicus (Karaman, 1922) to Triturus macedonicus (Karaman, 1922).


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