The few attempts to produce artificial hybrids in the genus Hieracium s. str. have usually failed due to the use of polyploid parental taxa reproducing via agamospermy. Presented here for the first time are data on artificial hybridization in Hieracium s. str. which may help in understanding the microevolutionary processes resulting in the great morphological and genetic diversity in this genus. Diploid, sexually reproducing species (H. alpinum, H. pojoritense, H. transsilvanicum and two stable morphological types of H. umbellatum – of a low altitude and a high mountain type) were used as parent plants in experimental crosses. In most cases true hybrids, with intermediate morphology, were obtained. All the hybrids tested were diploid and produced a high amount of stainable pollen (65–92%). Hybrid progeny resulting from one cross exhibited a large range of morphological variation due to the combination of alleles from unrelated parental species. The percentage of welldeveloped achenes per capitulum, in capitula with at least one well-developed achene, in hybrids, ranged from 1.9 to 12.5% after free or controlled pollination, with an average of 4–5% per capitulum. Similar results (1.9–12.1%) were obtained from triple-cross hybrids. However, most of the capitula of hybrid progeny (either F1 or triple) were completely sterile after free or controlled pollination. Sterility is probably caused by genome incompatibility of unrelated parental taxa belonging to different sections. In two crosses, where strictly allogamous diploid plants of H. umbellatum (both morphotypes) were used as mother plants and F1 hybrids as pollen donors, some matroclinal progeny were obtained. This is a further example of the previously reported mentor effect. Diploid hybrids may be involved as pollen donors in gene flow as they produce uniformly sized and viable pollen. They are probably substantially less important as seed parents.
Two new apomictic triploid (2n = 3x = 51) species from the Sorbus latifolia group, S. portae-bohemicae M. Lepší, P. Lepší, P. Vít et K. Boublík and S. albensis M. Lepší, K. Boublík, P. Lepší et P. Vít, putative hybridogenous species originated from a cross between S. danubialis and S. torminalis, are distinguished and described based on a taxonomic and chorological revision of Sorbus bohemica (a hybridogenous triploid species from the same parental combination). A number of contemporary biosystematic techniques, including molecular (nuclear microsatellite markers), karyological (chromosome counts, DAPI flow cytometry) and multivariate and geometric morphometrics were used to assess the variation of the species and justify their independent taxonomic status. All three species occur sympatrically in the České středohoří Mts (NW Bohemia). Sorbus bohemica is recorded from 31 localities, based on a revision of herbarium vouchers and field research. Recent field studies failed to verify five of these localities. Sorbus portae-bohemicae is a stenoendemic in the Porta bohemica gorge (situated ca 7 km WNW of Litoměřice) where it grows in open oak forests (Luzulo-Quercetum and transition vegetation type to Melampyro nemorosi-Carpinetum) on ENE-facing slopes and rocks. The only known population of S. portae-bohemicae consists of 14 adult individuals. Sorbus albensis occurs at 12 localities W to NW of Litoměřice. The total number of individuals is estimated at 600. Most are in acidophilous oak forests (Luzulo-Quercetum and its mesic derivatives), scree forests (Aceri-Carpinetum) or shrubby slopes (Pruno-Ligustretum, Antherico-Coryletum). Populations of the new taxa show little genetic variation and are phenotypically homogenous and well separated from other Bohemian hybridogenous Sorbus species. A distribution map of the three species is provided. Photographs of the type specimens and in situ fructiferous individuals of the new species are presented.
We studied the agamic complex of Hieracium subgen. Pilosella in the Šumava/Böhmerwald, the borderland between the Czech Republic and Germany. Their DNA ploidy levels/chromosome numbers, breeding systems, chloroplast haplotypes as well as the clonal structure of apomicts were determined. The complex consists of the following basic and intermediate species and recent hybrids. Basic species: H. aurantiacum L. (tetraploid and pentaploid, both apomictic), H. caespitosum Dumort. (tetraploid, apomictic), H. lactucella Wallr. (diploid, sexual), H. pilosella L. (tetraploid, sexual); intermediate species: H. floribundum Wimm. et Grab. (tetraploid, apomictic), H. glomeratum Froel. (tetraploid and pentaploid, both apomictic), H. scandinavicum Dahlst. (tetraploid, apomictic); recent hybrids: H. floribundum × H. pilosella (partly corresponding to H. piloselliflorum – tetraploid and hexaploid; tetraploid sexual or apomictic), H. glomeratum × H.pilosella (aneuploid, 2n = 38), H. aurantiacum × H. floribundum (tetraploid, almost sterile or apomictic), H. lactucella × H. pilosella (H. schultesii, triploid sterile, tetraploid sexual), H. aurantiacum × H. pilosella (H. stoloniflorum, tetraploid, sexual), H. aurantiacum > H. pilosella (H. rubrum, hexaploid). The hexaploid hybrids between H. pilosella and H. floribundum or H. aurantiacum produced mainly polyhaploid progeny. Two trihaploid plants were found growing in the neighbourhood of their putative hexaploid maternal parent H. rubrum, which is the first record of polyhaploids of this subgenus in the field. Comparison with other mountain ranges (especially the Krušné hory/Erzgebirge, and Krkonoše) with an almost identical composition of basic species, revealed that the structure of the agamic complexes differ.
Sorbus eximia Kovanda, a hybridogenous species that originated from the parental combination S. torminalis and S. aria s.l., is thought to be an apomictic species, which includes diploid and tetraploid individuals. The present study confirmed the existence of only triploid individuals. A new tentatively apomictic triploid (2n = 3x = 51) species from the S. latifolia group: S. barrandienica P. Vít, M. Lepší et P. Lepší is described based on a revision of S. eximia. This species is assumed to have originated from a cross between S. danubialis or S. aria s.l. and S. torminalis. A wide palette of biosystematic techniques, including molecular (nuclear microsatellite markers) and karyological analyses (chromosome counts, DAPI flow cytometry) as well as multivariate morphometric and elliptic Fourier analyses, were used to assess the variation in this species and justify its independent taxonomic status. Allopatric occurrences of both species were recorded east of the town of Beroun in the Český kras, central Bohemia (Bohemian Karst). A distribution map of the two species is provided. Sorbus eximia occurs at four localities (the total number of adults and juveniles is 100 and 200, respectively) in basiphilous thermophilous oak forests (Quercion pubescenti-petraeae), mesic oak forests (Melampyro nemorosi-Carpinetum), woody margins of dry grasslands (Festucion valesiacae) and pine plantations. Sorbus barrandienica has so far been recorded at 10 localities (ca 50 adults). Recent field studies failed to verify two of these localities. It is mainly found growing on the summits of hills, usually in thermophilous open forests (Primulo veris-Carpinetum, Melampyro nemorosi-Carpinetum, Quercion pubescenti-petraeae) and woody margins of dry grassland. Its populations exhibit minimal genetic variation and are phenotypically homogeneous and well separated from other Bohemian hybridogenous Sorbus species. The epitype of S. eximia is designated here, and a photograph of the specimen is included. Photographs of the type specimens and in situ individuals, and line drawings of both species are presented.