Haploid parthenogenesis in facultatively apomictic Pilosella generated polyhaploid progeny (with half the maternal chromosome set) both in natural populations and garden experiments. Production of polyhaploids varied considerably among different species, hybridogenous species and hybrids. In the field (14 localities), the highest frequency of polyhaploids exceeded 80% of the total seed progeny produced by some recent hybrids. A similar diversity in the production of polyhaploids was also recorded in garden experiments. A two-step process by which new genotypes of both P. aurantiaca (tetraploid) and P. rubra (hexaploid) were formed under garden conditions during a polyploid–polyhaploid–polyploid cycle is described. In the first step, the maternal plants generated dihaploid and trihaploid F1 progeny, respectively. Although a substantive part of this polyhaploid progeny was either non-viable or sterile, the apomictic polyhaploids occasionally doubled their genome. Consequently, the F2 progeny resulting from the second step had a double ploidy level, identical to that of the original maternal parent. The complete process was autonomous, without contribution of pollen from parent genotype. This cycle necessarily implicates increasing homozygosity in F2 progeny compared to the original maternal polyploid plant. The probabilities of particular steps of this process occurring in Pilosella and the variation in polyhaploids are estimated and described, and the ability of polyhaploid plants to survive under field conditions discussed. Probability of the complete cycle (haploid parthenogenesis followed by doubling of the genome), which occurred under garden conditions in P. rubra, is estimated to be in the order of hundredths of percent. Despite this low probability, it can result in the production of new homozygous genotypes in populations of apomicts, especially in those occurring in disturbed habitats with little competition.
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.