Does Transport Matter? Functional Integration of the Pollen on the Fig Wasp Body in Active and Passive Pollination of...

The obligate mutualism between Ficus and its pollinating wasps provides a suitable system to investigate these dynamics because it encompasses two contrasting pollination modes: active and passive. Here we compared pollen traits in an actively pollinated fig tree, Ficus citrifolia, and a passively pollinated species, F. obtusiuscula, examining pollen both at anther presentation and after deposition on the bodies of their pollinating wasps. Pollen morphology, hydration-related behavior, cytology, and reserve composition were characterized using scanning electron microscopy (conventional and modified), light and transmission electron microscopy, histochemical assays, and viability tests. Across species, pollen traits at anthesis showed broad overlap in morphology, viability and major reserve classes, indicating that these characteristics are not consistently predicted by pollination mode alone. In both species, pollen was bicellular, harmomegathic and highly viable at presentation, consistent with resilience during transport. The main divergence emerged after pollen transfer to the pollinator. In the actively pollinated species, pollen recovered from wasp thoracic pockets exhibited pronounced intracellular remodeling, including vacuolization, starch depletion, lipid redistribution and localized cytoplasmic degradation. By contrast, pollen of the passively pollinated species retained a comparatively stable cytological organization after transport despite changes in reserve distribution. These results suggest that the more pronounced cytoplasmic reorganization observed in the pollen of the actively pollinated species after deposition on the wasp body may represent a preparatory phase for rapid germination following pollination, reflecting the stronger dependence of larval development on successful flower fertilization in actively pollinated figs. More broadly, our study provides the first comparative account of pollen structural and cytophysiological dynamics on fig-wasp bodies, linking pollen cell biology to pollinator-mediated dispersal and highlighting how different pollination strategies may impose distinct selective pressures on male gametophytes.