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In six 42-chromosomes taxa belonging to genus Orchis s. l. heterochromatin location and distribution and staining properties were analysed by means of C-banding and of the fluorochromes 4’-6-diamidino-2-phenylindole-2HCl (DAPI) and Hoechst 33258. Most species could be distinguished on the basis of heterochromatin amounts and distribution. In the species O. mascula and O. provincialis most DAPI-positive sites did not co-localize with C-bands. DAPI revealed bright fluorescence at telomeric or subtelomeric regions of numerous chromosomes of O. mascula and particularly large/bright blocks at the telomeres of O. provincialis. In O. x penzigiana (Orchis mascula ssp. ichnusae x O. provincialis) overall heterochromatin distribution followed that of the parental species. In Neotinea group all DAPI positive bands co-localize with C-bands, but have different distribution in the taxa analysed. Present and literature data indicate a high level of plasticity of heterochromatin organization in Orchis s. l., and suggest evolutionary pathways in agreement with recent molecular data.

Heterochromatin distribution in selected taxa of the 42-chromosomes Orchis s. l. (Orchidaceae)