Subgenome analysis of two southern hemisphere allotriploid species in Sphagnum (Sphagnaceae)

Abstract

Sphagnum ×australe s.l. and S. ×falcatulum s.l. are both cryptic species complexes of gametophytically allodiploid and allotriploid cytotypes, with the allodiploid cytotype being one parent of the respective allotriploid cytotype. Phylogenetic analyses of S. ×australe s.l. and S. ×falcatulum s.l. were undertaken using sequences from two plastid loci and cloned sequences from three nuclear loci. Subgenomes from three subgenera were detected in allotriploid S. ×australe. The haploid parent of allotriploid S. ×australe was S. fimbriatum (subg. Acutifolia). One of the two subgenomes contributed by allodiploid S. australe was associated with S. strictum (subg. Rigida); the parental species associated with the other subgenome could not be identified, either at the species level or in terms of subgenus association. It may represent an early diverging lineage of subg. Sphagnum or a previously undetected subgenus. Allotriploid S. ×falcatulum has subgenomes from two subgenera. This study confirms prior findings that S. cuspidatum (subg. Cuspidata) was the haploid parent of allotriploid S. ×falcatulum. One of the two subgenomes contributed by allodiploid S. ×falcatulum was associated with subg. Cuspidata (species unidentified) and the second was associated with subg. Subsecunda (species unidentified). Recurrent allopolyploidy appears to have been associated with the complex evolutionary processes (inter-subgeneric hybridization, interploidal hybridization, double allopolyploidy) which resulted in each of these two allotriploids. The highest level of divergence detected among the subgenomes in each of these Sphagnum allotriploids is comparable to the average genetic divergence reported for angiosperm allopolyploids.

Keywords:

• Allopolyploidy
• Interploidal hybridization
• Inter-subgeneric hybrids
• Recurrent allopolyploidy
• Sphagnum ×australe
• S. ×falcatulum

Acknowledgements

Genetic laboratory work was undertaken at the Duke Bryology Laboratory. I thank Sandra Boles for her assistance in the laboratory and Dr. A. Jonathan Shaw for access to the laboratory. The feedback from the revicwers was much appreciated. Funding for the project was provided by Ramapo College. The laboratory work was accomplished while the author was on sabbatical from Ramapo College. Taxonomic Additions and Changes: Nil.