Amir Ben Dov (Israel)
Mars Muusse (Netherlands)
armenicus 2cy Jan
armenicus 3cy Jan
armenicus sub-ad Jan
armenicus adult Jan
Phenotypic characterization, taxonomic rank and phylogenetic relationships of Armenian Gull Larus armenicus
Dorit Liebers & Andreas J. Helbig
published: Limicola 13-6, 1999 (in German, with English summary)
Fig 24: Reconstruction of geneology tree for armenicus and michahellis.
results on mitochondrial DNA in armenicus
The reconstructed genealogy (the evolutionary ancestry tree) of the michahellis/armenicus-haplotypes shows two distinct clusters. One cluster (Cluster II) consists of 9 haplotypes that were only found in armenicus at Tuz and Van Golu. The other cluster (Cluster I) consists of 11 haplotypes which all can be found in michahellis from the E Mediterranean but were also found at Tuz Golu (2 haplotypes) and at Beysehir Golu (one haplotype).
The frequency of occurrence of these two cluster of haplotype-groups over the colonies is represented in Fig. 25 (Cluster I is white; Cluster II is black). It is immediately obvious that there were no armenicus haplotypes found in michahellis breeding along the coast of the Mediterranean or the Black Sea (but more study east of Crete and larger sample sizes are needed). The reverse is obvious as well: michahellis haplotypes do occur in colonies in interior Turkey, even in the phenotypically ‘pure’ armenicus colony of Tuz Golu (14% of the examined birds from this population show michahellis-type haplotypes). In the phenotypically mixed colony of Beysehir, even 62% of the birds have michahellis-type haplotypes. At Van Golu, where 30 birds (chicks from different nests) were examined, no such haplotypes were found (but this does not completely exclude the possibility of occurrence at this site; a larger sample size should reveal this).
Phylogenetically, Armenian Gull was found to be most closely related to michahellis to the exclusion of taymirensis, barabensis and cachinnans (Fig. 24). Michahellis and armenicus are represented by two distinct clusters in the mitochondrial haplotype phylogeny, but introgression (unidirectional geneflow) was evident with two michahellis haplotypes (shaded in cluster I, Fig. 24) having invaded the armenicus population at Tuz Golu. These and a third michahellis haplotype were found in 62% of the birds in Beysehir, 14% at Tuz and 0% at Van Golu (Fig. 25). This indicates that hybridization does occur, hybrids are fertile and backcross at least with armenicus in central Anatolia. Whether geneflow in the other direction (into the michahellis population of the E Mediterranean) also occurs requires further study. Notwithstanding the ongoing introgression, the phenotypically “pure” armenicus population at Tuz and Van Golu was genetically significantly differentiated from michahellis (AMOVA: ФST = 0.7857; p < 0.0001). The genetic divergence of the two haplotype clusters (average 2,05% at 420 nucleotides of control domain I, Fig. 26) indicates a relatively ancient separation and long independent evolution between michahellis and armenicus, but this has so far not resulted in full reproductive isolation.