Abstract
Floral key innovations play a significant role in the discussion of adaptive radiation in plants. The paper brings together a brief review of morphological key innovations in plants, elucidating their evolutionary significance in flower–pollinator interactions, and new data on Salvia, a genus being examined as an example for presumed adaptive radiation. We hypothesize that the characteristic staminal lever mechanism functions as a key innovation. It is defined as a functional unit including the modification of stamens to lever-like structures, their reversible movement, and the organization of the remaining floral structures involved in the process of pollen transfer. We follow the assumption that structure and functioning of the staminal levers play a major role in the process of pollen deposition on the pollinator's body, and that minute changes of both their proportions and their interactions with pollinators may have significant consequences for the pollination system. The functioning of the staminal lever mechanism is tested by field investigations, biomechanical experiments and pollination simulations. First results are presented, and possible modes of allopatric and sympatric speciation are discussed, based on morphometry of Salvia flowers and pollinators as well as on the operating mode of the staminal lever mechanism. Special attention is given to species-specific patterns of pollen deposition on the pollinator's body. We assume that, depending on the precision of the lever movement, sympatric Salvia species flowering during overlapping periods and sharing the same pollinating species may be either mechanically isolated from each other or able to hybridize. The latter may result in speciation, as may spontaneous mutations influencing the flower-pollinator interaction, e.g. by significant changes in morphometry of the staminal lever system and/or other flower structures. As a consequence, Salvia individuals may deposit pollen on a different part of the pollinator's body, or even adapt to a new pollinator species, both resulting in reproductive isolation from the parental population.
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