The exploration of the origin and diversification of angiosperms has entered an exciting new era. Fresh insights and new results are rapidly accumulating from paleobotany and a wide spectrum of botanical disciplines, and an increasing number of phylogenetic models for seed plant and angiosperm relationships are being developed. Current phylogenetic hypotheses broadly support previous views that the most basal angiosperm taxa fall within a grade of organization corresponding to the subclass Magnoliidae; however, there are divergent views on the resolution of relationships within the magnoliid grade. In part, discrepancies among the results from different analyses reflect difficulties in the polarization of critical reproductive characters, which arise because of the substantial morphological gap between angiosperms and other seed plants and the absence of important angiosperm features (e.g., carpel) in their closest seed plant relatives. These problems are also compounded by the extreme floral diversity among extant Magnoliidae, which ranges from the minute and naked, unisexual, unistaminate/unicarpellate flowers of Hedyosmum (Chloranthaceae) to the large bisexual and multipartite flowers of Magnolia (Magnoliaceae).Despite uncertainties in resolving relationships at the base of the angiosperm phylogenetic tree some consensus on patterns of character evolution is beginning to emerge. In particular there are strong indications from the study of fossil material that small, simple flowers may be basic in angiosperms, rather than larger multipartite floral structures similar to those of the woody Magnoliaceae [1][2][3][4]. This result is broadly congruent with several recent phylogenetic analyses of extant angiosperms based on comparative morphology [5][6][7], as well as phylogenetic analyses of molecular data [8][9][10]. Several authors now support the