Because of its presumed high levels of dioecy (separate male and female plants), study of the native Hawaiian angiosperm flora has been important in development of many hypotheses about conditions favoring the evolution of dioecy. The importance of ecological correlates with dioecy has proven difficult to assess, however, because of lack of data on the origins of dioecy in the Hawaiian Islands. Clearly, these correlations are of greater interest in taxa where dioecy evolved in the Hawaiian Islands (autochthonous evolution of dioecy) than in taxa that are the result of dioecious colonists with subsequent speciation in the Hawaiian Islands. Because the Hawaiian flora is small and extremely isolated, colonists can be identified and their breeding systems hypothesized, thus allowing inferences on the origins of dioecy. Using current taxonomic information, the incidence of dioecy in native Hawaiian angiosperm species is 14.7%, lower than previous estimates, but still the highest of any known flora worldwide. Ten percent of the colonists were sexually dimorphic (dioecious, gynodioecious, polygamodioecious, and subdioecious), and over half (55.2%) of current dimorphic species are in lineages arising from dimorphic colonists, showing that dimorphism is high in part because colonists were dimorphic. Autochthonous evolution of dimorphism occurred in at least 12 lineages (e.g., hermaphroditic colonists of Bidens (Asteraceae), the Hawaiian Alsinoideae (Caryophyllaceae), and Hedyotis (Rubiaceae) led to species—rich lineages that include many dimorphic species). One—third (31.8%) of current dimorphic species are in lineages arising from monomorphic colonists. Dioecy in the Hawaiian Islands is a result of both dimorphic colonists as well as evolution of dioecy in Hawaiian lineages from hermaphroditic colonists. The high incidence of dimorphism is not because dimorphic colonists evolved more species per colonist than monomorphic colonists. Detailed studies of individual lineages are critical to elucidate causal factors in the evolution of dioecy.
The angiosperm flora of the Hawaiian Islands, with its high incidence of dioecy, has been central in development of hypotheses about the evolution of dioecy. Based on a recent taxonomic treatment of the Hawaiian angiosperm flora, we analyzed biogeographic patterns of dioecy as well as the association of dioecy with ecological traits potentially important in the evolution of dioecy for native current species and genera. We also analyzed patterns for presumed colonists of the flora to control better for phylogenetic patterns in these traits. Dioecy is associated with woodiness, especially trees; however, this pattern does not hold for gynodioecy. Within woody species, dimorphism (dioecy, gynodioecy, subdioecy, polygamodioecy) is associated with mesic habitats and occurs more frequently in species with lowland and lowland—montane distributions. In contrast, in the endemic Hawaiian Alsinoideae (Schiedea and Alsinidendron) and in Bidens (two groups with autochthonous evolution of dimorphism), dimorphism is associated with more xeric habitats, and for the former group, with wind pollination. For the entire angiosperm flora, dimorphic species are associated with flowers that are small and green. Woody dioecious species and genera are disproportionately associated with wind pollination; hermaphroditic species are disproportionately bird pollinated primarily because of one species—rich lineage in the Campanulaceae. There was no association of dimorphism and pollinator type for colonists. Because of a few species—rich lineages, dimorphism is associated with dry fruits at the specific level, but at the generic level and for colonists, dimorphism is associated with fleshy fruits. Dioecious and gynodioecious species are found more often on older islands, a result of speciation of dimorphic colonists as well as autochthonous evolution of dimorphism. Single—island endemism is not associated with dioecy in the flora as a whole or with dimorphism within lineages evolving dimorphism autochthonously; thus Baker's law is not supported within the Hawaiian Islands. Because the Hawaiian angiosperm flora originated from a minimum of only 291 colonists, many of the associations of dimorphism with ecological traits occur because of the influence of only a few species—rich lineages. Better knowledge of phylogenetic patterns and further ecological studies, particularly within those groups evolving dioecy autochthonously, are needed to determine causality.
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