A taxonomic study of the Pilosella alpicola group growing in the Carpathians revealed the presence of two morphologically distinguishable taxa: P. ullepitschii (Błocki) Szeląg and P. rhodopea (Griseb.) Szeląg. While P. ullepitschii is endemic to the Carpathians, P. rhodopea is a Balkan subendemic with two isolated localities in the Southern Carpathians (Mt Cozia and Mt Zmeuretu). The core area of distribution of P. ullepitchii is the natural subalpine and alpine meadows of the Western Carpathians (the Vysoké and Západné Tatry Mts in Slovakia and Poland). In addition, only three isolated localities are known from the Nemira Mts (Romanian Eastern Carpathians) and one from the Bucegi Mts (Romanian Southern Carpathians). Interestingly, the Romanian populations occur in man-made habitats (secondary pastures). Karyological and flow cytometric analyses of 305 plants from 13 populations of P. ullepitschii revealed only diploid plants (2n = 2x = 18). One Carpathian population of P. rhodopea from Mt Cozia is also diploid. This is the first report of diploidy in this species. However, the populations from the main part of the distribution of this taxon in the Balkan mountains include other cytotypes. Detailed morphological descriptions and distributions for both taxa are given.
Four European taxa of the Tortula muralis complex (T. lingulata, T. muralis var. aestiva, T. muralis var. muralis, T. obtusifolia) were evaluated using multivariate analysis of morphological characters, a cultivation experiment and cytological screening (flow cytometry, chromosome counts). This study revealed that only T. lingulata is morphologically well defined within the complex and several new sporophytic characters that can be used to distinguish this taxon from the superficially most similar T. obtusifolia. The traditionally recognized taxa T. muralis var. muralis, T. muralis var. aestiva and T. obtusifolia showed continuous variation, with frequent intermediate plants. However, the main character of the gametophyte used for determination (costa excurrency) proved to be stable in cultivation, indicating that this character is under genetic control. Additionally, rather complex and only partly species-specific patterns of ploidy variation were found within the complex. Tortula lingulata and T. obtusifolia appear to be cytologically homogeneous; plants of T. lingulata were found to be diploid, whereas plants tentatively named as T. obtusifolia were haploid. In contrast, both haploid and diploid cytotypes were found in both varieties of T. muralis, with a marked predominance of diploids in var. aestiva and less marked predominance of diploids in var. muralis. Current varietal level of the evaluated infraspecific taxa of T. muralis was thus found to be warranted. It is suggested that plants previously recognized as T. obtusifolia should be treated as a subspecies of T. muralis.
Perennial grasses belonging to the genus Molinia are widespread in most of Europe and consist of a polyploid complex of closely related taxa with a confusing taxonomy. Based on extensive sampling at 241 localities in Europe, four cytotypes were identified based on chromosome counts and results of flow cytometry: tetraploids (2n = 36), hexaploids (2n = 54), octoploids (2n = 72) and dodecaploids (2n = 108). While tetra- and dodecaploids were commonly recorded, octoploids were less common and only two hexaploid individuals were identified. Previously reported decaploid counts (2n = 90) from central Europe are probably erroneous and refer to 2n = 108. The tetraploid cytotype is distributed throughout Europe and broadly sympatric with other cytotypes. Octo- and dodecaploids were spatially separated with dodecaploids occurring in the western, central and south-central part of Europe and octoploids in the east-central and southeastern part of Europe. All quantitative characters measured (lengths of lemmas, anthers, caryopses and stomata, lengths of the longest hair on the callus and diameter of the culm below the panicle) showed a linear trend across ploidy levels. Tetra-, octo- and dodecaploid cytotypes formed almost non-overlapping groupings in principal component and discriminant analyses of morphological characters. The following taxonomic concept of this complex is proposed: Molinia caerulea (L.) Moench is a predominantly tetraploid taxon incorporating very rarely reported hexaploid and perhaps also diploid plants; higher cytotypes (2n = 8x, 12x) are considered to be M. arundinacea Schrank, consisting of two subspecies: a dodecaploid subspecies occurring in the southern and western part of central Europe and the octoploid Molinia arundinacea subsp. freyi Dančák in east-central and southeastern Europe.
As a result of inconsistencies in morphological characters, Cerastium pumilum and C. glutinosum have been misunderstood or confused in many European floras since the 1960s. In the second volume of the Flora Nordica, a revised treatment of C. pumilum s.l. is provided and this concept is tested here for eastern Central European populations. The cytometric and morphological part of the study is based on living plants from 85 populations in the Czech Republic, Slovakia, Poland, Austria and Hungary. Flow cytometric analyses of the samples revealed two groups differing in ploidy level and corresponding to two cytotypes (a known octoploid, 2n ≈ 72, for C. glutinosum and yet unknown dodecaploid, 2n ≈ 108, for C. pumilum). Eleven morphological characters were scored or measured in plants of known ploidy level and the data set analysed using multivariate statistics (principal component analysis and canonical discriminant analysis); the two morphologically well-separated groups were identical with the two cytotype groups detected by flow cytometry. Based on these results, we suggest treating the detected cyto-morphotypes as the species C. pumilum and C. glutinosum. Our analysis further revealed that the traditionally used characters (glabrous vs. hairy adaxial surface and presence vs. absence of a scarious margin to the tip of the lowermost bracts) are not taxonomically informative. The characters best differentiating the species include indument on the lowermost vernal internodium, length of mature stylodia, length of glandular hairs on sepals and maximum diameter of mature seed. A key for identification of both species is also provided. A revision of almost 1600 specimens deposited in 16 Central European herbaria revealed that the species show different distribution patterns in Central Europe and partial habitat segregation. Specimens from the Czech Republic previously assigned to C. litigiosum were identified as C. pumilum; consequently, C. litigiosum must be removed from the Czech flora.
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.