Chromosome numbers are given for 16 taxa (and one interspecific hybrid) of Hieracium subgen. Pilosella originating from Central Europe: H. apatelium Nägeli et Peter (2n = 45), H. aurantiacum L. (2n = 36), H. bauhini Besser (2n = 36, 45, 54), H. brachiatum Bertol. ex DC. (2n = 45, 48, 63, 72), H. densiflorum Tausch (2n = 36), H. echioides Lumn. (2n = 18, 27, 36), H. floribundum Wimm. et Grab. (2n = 36, 45), H. glomeratum Froel. (2n = 36, 45), H. guthnickianum Hegetschw. (2n = 54), H. lactucella Wallr. (2n = 18), H. onegense (Norrl.) Norrl. (2n = 18), H. pilosella L. (2n = 36, 45, 54), H. piloselliflorum Nägeli et Peter (2n = 36, 45), H. piloselloides Vill. (2n = 36), H. rothianum Wallr. (2n = 36), H. schultesii F. W. Schultz (2n = 45), and the hybrid H. floribundum × H. aurantiacum (2n = 36). New chromosome numbers are reported for H. brachiatum and H. floribundum. The octoploid cytotype (2n = 72), recorded in H. brachiatum, is the highest ploidy level ever found in plants from the subgen. Pilosella originating from the field. Aneuploidy, rare in this subgenus in Europe, occurs in this hybridogenous species as well: it was recorded in one plant (2n = 48) collected in a hybrid swarm H. pilosella × H. bauhini. The breeding system in H. bauhini, H. brachiatum, H. densiflorum, H. echioides, H. pilosella, H. piloselloides, and H. rothianum was studied. The sexual reproduction of pentaploid H. pilosella is a new observation: it means an increase of diversity in possible reproduction modes of those cytotypes having odd chromosome numbers.
Chromosome numbers (ploidy levels) were recorded in the following 25 taxa of Hieracium subgen. Pilosella: H. arvicola Nägeli et Peter (2n = 45), H. aurantiacum L. (2n = 36, 45), H. bauhini Besser (2n = 36, 45), H. bifurcum M. Bieb. (2n = 45), H. brachiatum Bertol. ex DC. (2n = 36, 45), H. caespitosum Dumort. (2n = 36), H. cymosum L. (2n ~ 4x), H. densiflorum Tausch (2n = 36, ~ 4x), H. echioides Lumn. (2n = 18, 45), H. fallacinum F. W. Schultz (2n = 36, 45), H. floribundum Wimm. et Grab. (2n = 36, ~ 4x, 45,), H. glomeratum Froel. in DC. (2n = 45), H. iseranum Uechtr. (2n = 36), H. kalksburgense Wiesb. (2n ~ 5x), H. lactucella Wallr. (2n = 18), H. macranthum (Ten.) Ten. (2n = 18), H. onegense (Norrl.) Norrl. (2n = 18), H. pilosella L. (2n = 36, 45, 54), H. piloselliflorum Nägeli et Peter (2n = 45), H. pilosellinum F. W. Schultz (2n = 36, 45), H. piloselloides Vill. (2n = 27, 36, ~ 4x, 45, ~ 5x), H. pistoriense Nägeli et Peter (2n = 27), H. rothianum Wallr. (2n ~ 3x), H. schultesii F. W. Schultz (2n = 36, 45, ~ 5x), H. zizianum Tausch (2n = 27, 36, 54), and one hybrid, H. onegense × H. pilosella (2n = 36). Besides chromosome counts in root-tip meristems, flow cytometry was used to determine the DNA ploidy level in 83 samples of 9 species. The presence of a long marker chromosome was confirmed in tetraploid H. caespitosum and H. iseranum, in pentaploid H. glomeratum, and in both tetraploid and pentaploid H. floribundum. The documented mode of reproduction is sexual (H. densiflorum, H. echioides, H. piloselloides) and apomictic (H. brachiatum, H. floribundum, H. pilosellinum, H. piloselloides, H. rothianum, H. zizianum). Hieracium bifurcum and H. pistoriense are sterile. The chromosome number and/or mode of reproduction of H. bifurcum (almost sterile pentaploid), H. pilosellinum (apomictic pentaploid), H. piloselloides (apomictic triploid), H. pistoriense (sterile triploid), H. rothianum (apomictic triploid) and H. zizianum (apomictic triploid) are presented here for the first time. The sexual reproduction recorded in the pentaploid H. echioides is the second recorded case of this mode of reproduction in a pentaploid cytotype of Hieracium subgenus Pilosella. A previously unknown occurrence of H. pistoriense (H. macranthum – H. bauhini) in Slovakia is reported.
Chromosome numbers were determined for 97 samples of 95 sedge taxa (Carex) from the following countries: Austria (6 records), Bulgaria (1), the Canary Islands (Spain, 1), Cape Verde (1), the Czech Republic (51), Hungary (1), Italy (2), Norway (8), Russia (15), Slovakia (1), Sweden (1) and 9 North American plants cultivated in Czech botanical gardens. Chromosome numbers for Carex argunensis, C. callitrichos, C. campylorhina, C. flavocuspis subsp. krascheninnikovii, C. paniculata subsp. hansenii, C. pallida, C. quadriflora and C. xiphium are reported here for the first time. The first reports are presented for the European portion of the distribution area of Carex obtusata and for the Central European portion of the distributional areas of C. chordorrhiza, C. otrubae, C. rhizina and C. strigosa. New counts for the Czech Republic fill the gaps in the karyological data for this genus in relation to the Flora project in the Czech Republic.
Pollen viability was analysed causally between and within Central European Cirsium species and their hybrids to determine (i) how frequently hybrids are fertile and produce viable pollen; (ii) how the pollen viability of hybrids and their parents are related and how this is affected by the genetic distance between parents; (iii) how species promiscuity relates to species pollen viability; (iv) to what extent the pollen viability of a hybrid may predetermine its frequency in nature; (v) how the pollen viability of a hybrid and sympatricity of its parental species are related; and (vii) how the frequency of females in populations of gynodioecious species may affect the observed pollen viability. Altogether, the viability of 656,363 pollen grains was analysed using Alexander’s staining (1185 flowers from 301 plants from 67 field populations of 13 pure species and 1693 flowers from 345 plants from 96 field populations of 16 natural hybrids). The particular characters potentially related with pollen viability were estimated using following methods: natural hybrid frequency and species interfertility (by herbarium data), genetic distance (by AFLP), sympatricity (in local scale based on herbaria and literature data; on a global scale using the similarity between digitized maps of natural ranges). The strengths of pre- or postzygotic isolation were estimated for hybridizing species pairs using geographical data and pollen viability analyses. All hermaphrodite plants of the Cirsium hybrids had viable pollen, generally at lower levels than those found in pure species. The pollen viability of a hybrid generally decreased with increasing genetic distance between the parents and when the parental species had lower pollen viability. The pollen viability was decreased in frequently hybridizing species where occasionally individuals of pure species morphology may show decreased pollen viability. In some instances these might represent some unrecognized hybrid backcrosses. In populations of gynodioecious species where females co-occurred, pollen viability (in hermaphrodites)was also lower, indicating some degree of inbreeding depression. Hybrids between sympatric species exhibited higher post-pollination isolation (decrease of pollen viability), which suggests that the reproductive isolation had been increased by natural selection (effect similar to the Wallace effect). The strength of the postzygotic barrier (based on pollen viability) was generally stronger than that of the prezygotic barrier (based on distribution overlap) in studied hybridizing species pairs.
This paper reviews recent use of flow cytometry in studies on apomictic plant taxa. The most of apomictic angiosperms are polyploid, often differing in ploidy level from their sexual counterparts within the agamic complex. Flow cytometry is widely used for screening the ploidy levels of mature plants and their seed generated both in the field and in experiments. Routine ploidy screening often accompanied by molecular markers distinguishing individual genotypes are used to reveal novel insights into the biosystematics and population biology of apomictic taxa. Apomixis (asexual seed formation) is mostly facultative, operating together with other less frequent reproductive pathways within the same individual. The diversity in modes of reproduction in apomicts is commonly reflected in the ploidy structure of their progeny in mixed-cytotype populations. Thus, flow cytometry facilitates the detection and quantification of particular progeny classes generated by different reproductive pathways. The specific embryo/endosperm ploidy ratios, typical of the different reproductive pathways, result from modifications of double fertilization in sexual/apomictic angiosperms.Thus, the reproductive origin of seed can be identified, including autonomous or pseudogamous apomixis, haploid parthenogenesis and sexual reproduction, involving either reduced or unreduced gametes. Collectively, flow cytometry has been used to address the following research topics: (i) assessing the variation in ploidy levels and genome sizes in agamic complexes, (ii) detection and quantification of different reproductive modes in facultative apomicts, (iii) elucidation of processes in populations with coexisting sexual and apomictic biotypes, (iv) evolution of agamic complexes, and (v) genetic basis of apomixis. The last topic is of paramount importance to crop breeding: the search for candidate gene(s) responsible for apomixis is the main objective of many research programmes. A list of the angiosperm taxa that could provide model systems for such research is provided.