Jerzy Szweykowski

Conocephalum salebrosum (Marchantiopsida, Conocephalaceae) - a new Holarctic liverwort species

Detailed analysis of 270 specimens of Conocephalum conicum (L.) Dumort., mainly from the POZW Herbarium revealed some diagnostic differences between two cryptic species originally detected on the basis of isozyme studies. Several diagnostic characters were found in the structure of the archegoniophore, sporophyte and sterile thallus. The most reliable diagnostic features are size and structure of stomatal apparatus of the archegoniophore ‘heads’, type of junction of the air chamber walls with epidermal cells, and the thallus surface details. On the basis of morphological and anatomical diagnostic characters, two formerly cryptic species are recognized following the rules of formal taxonomy. The lectotype of C. conicum preserved in FI was found to possess characteristics of cryptic species C. conicum- species L. Accordingly, the species previously named as C. conicum–species L must bear the name Conocephalum conicum (L.) Dumort. No published name was related to C. conicum – species S, which is therefore described as a new species: Conocephalum salebrosum Szweykowski, Buczkowska & Odrzykoski. Both species are fully described and their diagnostic characters are illustrated. Distribution maps for both species are given.

Genetic differentiation without concordant morphological divergence in the thallose liverwort Conocephalum conicum

Allozyme variation was examined at 33 enzyme loci for 96 populations from throughout the geographical range ofConocephalum conicum (L.)Dum. (Marchantiales, Hepaticae). Variation was partitioned into five discrete groups, suggesting that this morphologically defined species is genetically heterogeneous. The degree of differentiation among these groups, as measured by genetic distance, is as large as is commonly reported between different vascular plant species, and much larger than that between conspecific populations. In Europe, two of these genetically distinct groups (S and L) occur sympatrically, but apparently do not interbreed. Geographical ranges of the other three groups (A, C, and J) are probably allopatric with the exception that the range of S, the most genetically divergent group, overlaps with group A in N. America. It is suggested that these five natural assemblages constitute different sibling species.

The hybrid origin of the polyploid liverwort Pellia borealis

Isozyme markers were used to investigate the origin of the polyploid liverwort, Pellia borealis (gametophytic n=18), which was believed to represent an autopolyploid form of Pellia epiphylla (n=9). Enzyme variation was studied in four taxa: polyploid P. borealis, two recently discovered sibling species of P. epiphylla complex, and the closely related P. neesiana (n=9). Gametophytes of the polyploid showed a complex electrophoretic phenotype for three diagnostic enzymes (DIA1, MPI1 and ACO) in contrast to simple pattern in all haploid taxa. It was postulated that the pattern found in the polyploid represents a ‘fixed heterozygous’ phenotype resulting from allopolyploidy. Alleles present in the polyploid were found (with only one exception) in the two sibling species of the P. epiphylla complex, suggesting that they are the parents of the allopolyploid. Pellia neesiana was excluded as a donor of either of the genomes. Variation in the polyploid suggests at least three separate origins of P. borealis.

Phylogeny of the European species of the genus Pellia (Hepaticae; Metzgeriales) based on the molecular data from nuclear tRNA(Leu)(CAA) intergenic sequences.

Species of the genus Pellia are similar to such an extent that their proper recognition based on morphological and anatomical features is difficult. To solve this problem isozyme methods were developed. As a result of these studies new cryptic species were recognized and new hypotheses concerning phylogenetic relationship in Pellia were formed. To examine hypotheses derived from isozyme data we decided to study species of the genus Pellia at the DNA level. Total DNA from all Polish Pellia species was isolated. The taxonomic and phylogenetic relationships in Pellia were examined using intergenic spacer sequences between nuclear tRNA(Leu) genes organised in tandem arrays. PCR (polymerase chain reaction) amplification of tRNA(Leu) gene spacers produced fragments of different sizes in all species and their restriction analysis showed species-specific patterns. PCR products were cloned and sequenced. Nucleotide sequence data were used for phylogenetic reconstruction. Sequence analysis confirmed previous results based on isozyme studies that P. endiviifolia- species A and species B as well as P. epiphylla- species S and species N (having different isozyme multilocus genotypes) are separate sibling species. Our results also confirmed the allopolyploid character of the only polyploid species in Pellia, P. borealis which was formed by hybridization of P. epiphylla- species N and P. epiphylla- species S cryptic species.