Morphometric and cytological data were used to test the variation within the apomictic hybrid Sorbus meinichii from its type locality, in the Moster area, Bømlo in Sunnhordland, Norway. A lectotype is selected for the name. A total of 36 morphological characters were measured on leaves, stomata, flowers, pollen, fruits and seeds, from randomly selected S. meinichii individuals. In the field the material was classified into two groups, one including individuals of generally larger dimensions of leaves and fruits than the other. The preliminary classification was subsequently tested by a multivariate analysis of several characters, substantiating the existence of two morphs in the population at the type locality of S. meinichii, one corresponding to the selected lectotype. Assessment of the nature and taxonomic rank of these two morphs must await further studies. Cytological studies showed both forms of S. meinichii to be triploid, with 2n=51 chromosomes. The taxonomic separation of S. teodorii from S. meinichii on the basis of ploidy level is therefore not corroborated. Sorbus meinichii s. lat. was shown to be intermediate between its supposed parents, S. aucuparia and S. hybrida, in several leaf characters. All of the variation within the S. aucuparia×S. hybrida‐complex in Fennoscandia is better included in one aggregate species Sorbus meinichii according to the present state of knowledge.
Rosa spinosissima is an endangered species in Norway, found only within a limited area on the southwestern coast. Presumed hybrid forms between R. spinosissima and rose species within R. sect. Caninae have been recorded from this area since the late 19th century. Here, analyses of such hybrid plants and selected populations of the tentative parent species were performed using AFLP markers, nuclear DNA content, pollen viability and seed germination rates, in addition to classic morphometric analysis. It is established that the hybrid rose represents a single hybrid taxon, viz Rosa sabinii, formed by recurrent asymmetrical hybridization events between R. spinosissima and R. mollis, with the latter being the obligate ovule donor. The evidence presented does not indicate hybridization with other co-occurring rose species, or of introgression from R. mollis into R. spinosissima through backcrossing with R. sabinii.
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