Ps. Soltis et al., MOLECULAR PHYLOGENETIC ANALYSIS OF THE HAWAIIAN ENDEMICS SCHIEDEA ANDALSINIDENDRON (CARYOPHYLLACEAE), Systematic botany, 21(3), 1996, pp. 365-379
Schiedea and Alsinidendron (Caryophyllaceae), which represent the fift
h or sixth largest endemic radiation of species in the angiosperm flor
a of the Hawaiian Islands, exhibit striking diversity in morphology, b
reeding system, and habitat. To gain a historical perspective on this
diversity, we conducted a phylogenetic analysis using restriction site
variation in chloroplast DNA and nuclear ribosomal DNA. In addition,
we compared, and ultimately combined, the molecular data with a recent
ly published morphological data set. Within the Schieden-Alsinidendron
lineage, DNA variation is limited, and relationships are generally po
orly resolved. These results raise the possibility that, following the
initial colonization of the Hawaiian archipelago and the early divers
ification of the complex, much of the complex radiated rapidly and rel
atively recently. Phylogenetic analyses of DNA data revealed three cla
des within the complex (the S. membranacea, S. nuttallii, and S. adama
ntis clades), in agreement with results of a morphologically-based ana
lysis. Molecular data do not, however, support the S. globosa clade, a
weakly-supported clade based on morphology. A combined analysis of mo
rphological and molecular data provided both greater resolution and st
ronger internal support than either data set did individually. The mol
ecular and combined topologies suggest nearly identical patterns of th
e evolution of sexual dimorphism, habitat shifts, and biogeography wit
hin the complex. However, the greater resolution in trees derived from
the combined analysis suggests simpler patterns of breeding-system ev
olution and habitat shifts. Sexual dimorphism may have evolved twice i
n the complex, with a single reversal to hermaphroditism in one specie
s, or perhaps only once, with three reversals to hermaphroditism. Alth
ough the habitat occupied by the ancestor of the complex remains uncer
tain, it appears that a single shift to dry habitats more or less acco
mpanied the evolution of dimorphic breeding systems, followed by a sin
gle shift back to a mesic environment in one species. Alternatively, t
wo parallel shifts to dry habitats may have occurred. Molecular data a
re consistent with an origin on Kaua'i of the S. membranacea, S. adama
ntis, and S. nuttallii clades, as suggested by previous morphological
analyses. However, both the molecular and combined trees suggest it is
equally likely that the complex originated on O'ahu.