Flowering Biology of <i>Rhododendron pulchrum</i>

Abstract

To study the flowering biology of Rhododendron pulchrum, we used scanning electron microscopy (SEM) and paraffin sectioning to observe the microstructures of its floral organs, a methyl thiazolyl tetrazolium (MTT) colorimetric assay to detect pollen viability in different periods, continuous observations to study flowering phenology, and artificial pollination and a benzidine-hydrogen peroxide method to determine stigma receptivity. R. pulchrum exhibited a centralized flowering phenology. The protogynous stigmas of R. pulchrum were able to receive pollen before flowering. The pollen grains of R. pulchrum fused into tetrads, the average ratio of the polar axis length to the equatorial axis length (P/E) was 1.05, and the pollen viability was highest in the initial flowering period, reaching 88.98%. The pollen/ovule (P/O) ratio was 266–328, and the outcrossing index (OCI) was 4; the vitality of R. pulchrum pollen remained high in the initial flowering and blooming periods. Compared with the lifespan of a single flower, pollen vitality remained high for most of the experimental period, thereby improving male fitness. The P/O ratio suggests that R. pulchrum may have a facultative outcrossing breeding system. The OCI estimation suggests that R. pulchrum is partially self-compatible, most likely requiring pollinators to complete pollination.

Keywords

• <i>Rhododendron pulchrum</i>
• flowering phenology
• pollen
• breeding system
• reproduction