RECONSTRUCTION OF THE EVOLUTION OF REPRODUCTIVE CHARACTERS IN PONTEDERIACEAE USING PHYLOGENETIC EVIDENCE FROM CHLOROPLAST DNA RESTRICTION-SITE VARIATION
Jr. Kohn et al., RECONSTRUCTION OF THE EVOLUTION OF REPRODUCTIVE CHARACTERS IN PONTEDERIACEAE USING PHYLOGENETIC EVIDENCE FROM CHLOROPLAST DNA RESTRICTION-SITE VARIATION, Evolution, 50(4), 1996, pp. 1454-1469
We reconstructed the phylogenetic history of Pontederiaceae using chlo
roplast DNA restriction-site variation from approximately two-thirds o
f the species in this family of aquatic monocotyledons. The molecular
phylogeny was used to evaluate hypotheses concerning the evolution of
reproductive characters associated with the breeding system. The famil
y has four main genera, two of which (Eichhornia and Pontederia) have
tristylous, predominantly outcrossing species, while two (Monochoria a
nd Heteranthera) have enantiostylous taxa. Self-incompatibility is res
tricted to some but not all tristylous species. In Eichhornia and Pont
ederia, predominantly selfing species with small monomorphic flowers (
homostyly) have been hypothesized to result from the multiple breakdow
n of tristyly. Restriction-site variation provided a well supported ph
ylogeny of ingroup taxa, enabling the mapping of reproductive characte
rs onto trees. Two contrasting optimization schemes were assessed, dif
fering in the relative weights assigned to shifts in character states.
The reconstructed sequence of floral character-state change was used
to assess competing hypotheses concerning the origin and breakdown of
tristyly, and the relationships between tristylous and enantiostylous
syndromes. Our results indicate that the class of optimization scheme
used was the most critical factor in reconstructing character evolutio
n. Despite some topological uncertainties and difficulty in reconstruc
ting the primitive floral form in the family, several broad conclusion
s were possible when an unordered, unequally-weighted optimization sch
eme was used: (1) tristyly originated either once or twice, while the
occurrence of enantiostyly in Monochoria and Heteranthera was always f
ound to have independent origins; (2) tristyly has repeatedly broken d
own leading to selfing, homostylous taxa; and (3) self-incompatibility
probably arose after the origin of floral trimorphism, a sequence of
events that conflicts with some evolutionary models.