agreement with the previous conclusions of
Landolt (1986) and Les et al. (2002). The alternative explanation is that the mutation rates in
the species of this section are higher.
It is remarkable that the internal structure of
the genus Lemna evaluated by GBS is almost
identical to the structure evaluated on the basis of
morphological and phytochemical markers (Les
et al. 1997). All four sections were revealed as
monophyletic taxa and evaluated by very high
posterior probabilities. This confirms the conclusion of Les et al. (2002) which was drawn on
the basis of different PCR fragments. The high
resolution of the GBS markers in the genus
Lemna also indicates that the section levels
should be revised (Fig. 11.2). For example, to
merge L. section Alatae and L. section Biformes
or to separate L. section Lemna into several
subsections. As the number of clones investigated per species in the present study remains
small, the diversity within and between species
might have some gaps. By the same reasons, it
cannot be decided whether all ten species of the
genus Lemna outside of L. section Uninerves
should be considered as independent species.
Therefore, to finalise the revision of the sections,
we are expanding our current study by including
more clones per species.
Acknowledgements The technical assistance of Susanne
König, Ines Walde, Sandra Drießlein, and Christa Fricke
(all IPK Gatersleben, Germany) is highly acknowledged.
We also thank Ingo Schubert from IPK Gatersleben, who
had provided access to the molecular methods and Walter
Laemmler, Landolt Duckweed Collection, Zürich, for
providing some clones.
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