期刊
FLORA
卷 298, 期 -, 页码 -出版社
ELSEVIER GMBH
DOI: 10.1016/j.flora.2022.152199
关键词
Connective teeth; Bee pollination; Evolution; Floral morphology; Hummingbird pollination; Staminal lever
Salvia (Lamiaceae) is a widely distributed genus in Asia with approximately 1000 species. The species within Salvia employ a staminal lever mechanism, which has contributed to the diversification within the genus. However, the role and evolution of ventral outgrowths or connective teeth associated with this mechanism remain unclear. In this study, we examined the function of these teeth in pollination and provided an evolutionary scenario for their development. Our findings suggest that these teeth serve as pressure points and facilitate lever movement during pollination.
Salvia (Lamiaceae) is a sub-cosmopolitan genus of about 1000 species that often employ a staminal lever mechanism that is thought to have spurred species diversification within the genus. The function and evolution of ventral outgrowths or connective teeth, associated with the lever mechanism in some species of Salvia, is often unclear despite the wealth of pollination observations across the genus and the major role that pollinators play in driving diversification within the genus. We document the role of these teeth in pollination studies of beepollinated Salvia farinacea, examine connective teeth across other bee- and hummingbird-pollinated species of New World subg. Calosphace, and provide an evolutionary scenario for the connective teeth in context of the staminal lever. Our observations show that the larger teeth function as pressure points at the floral entrance and, when pressed by a pollinator, facilitate movement of the lever. Multiple shifts in pollinator within subg. Calosphace may have resulted in further modifications of the connective and possible further losses and independent origins of connective teeth in Calosphace. Other distantly related subgenera (e.g., Sclarea, Glutinaria) display morphologically and spatially different protuberances on the connective, suggesting that connective teeth only evolved near the base of subg. Calosphace.
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