Background <p>Cryptic dioecy is a sexual system in which individuals of at least one sex are morphologically hermaphroditic but functionally unisexual. The presence of non-functional reproductive organs may represent an intermediate stage during the evolutionary transition from hermaphroditism to dioecy. The ancestral hypothesis suggests that sterile sex organs may persist as vestiges of an ancestral bisexual state, potentially due to their low resource cost or absence of significant conflict with fertile organs, yet this has rarely been tested. All <i>Actinidia</i> species exhibit cryptic dioecy with morphological androdioecy, providing an ideal system for testing this hypothesis.</p> Methods <p>This study investigated floral traits and biomass allocation of floral organs across nine <i>Actinidia</i> taxa, and used phylogenetic independent contrasts (PIC) across 28 taxa to examine correlations among floral traits. The aims were to reveal the resource investment in sterile sex organs and their relationships with other floral structures, and to test the ancestral hypothesis.</p> Results <p>Although functionally female flowers of <i>Actinidia</i> are morphologically perfect, their pollen grains are sterile. Stamen number exhibited high interspecific variation in both floral morphs. The biomass allocation proportion to sterile stamens in functionally female flowers was significantly lower compared to that allocated to fertile stamens in male flowers. Furthermore, significantly positive correlations were observed between sterile and fertile sex organs across multiple traits in functionally female flowers, at both species and genus levels.</p> Conclusions <p>These results suggest that floral traits in <i>Actinidia</i> have evolved into a highly integrated modular structure. Sterile stamens in functionally female flowers have low resource costs and exhibit a synergistic effect during development or resource allocation with female organs. This study provides support for the ancestral hypothesis.</p>