Abstract

Pollinia of Cymbidium goeringii (Orchidaceae) were examined at a young stage (approx. 2 weeks before anthesis) and at anthesis using transmission electron microscopy, computer-assisted serial reconstruction and quantitative cytology. At the young stage, the generative cell (GC) has a spherically shaped main body with a large nucleus and 1 to 4 cytoplasmic extensions (up to 10 μm long) physically associated with a groove on one side of the vegetative nucleus (VN). By anthesis, some GCs lose their cytoplasmic extensions, becoming spherical. The GC surface becomes highly wrinkled, the distance between the GC and the VN increases and the two may separate completely. Enucleated cytoplasmic bodies (ECBs) are apparently generated by the GC, as evidenced by their similar ultrastructural appearance and distribution near the GC. ECBs are likely produced from two sites: the GC surface and the tips of cytoplasmic extensions of the GC. Vesicle-containing bodies (VCBs) may be generated from the lateral surface of the GC and may also represent a degeneration stage of ECBs, finally fusing with lipid bodies. Heritable organelles are rare and usually absent in the GC of Cymbidium: 0.176 mitochondria and 0.0042 plastids per GC were observed at the young stage and no mitochondria and 0.019 plastids at anthesis. Of 16 cellular parameters examined during GC development, all decreased with the exception of the surface area and volume of ECBs/ VCBs (which remained stable) and GC vacuoles (which increased). Significant decreases in 11 parameters presumably relate to dehydration of the pollen and male cytoplasmic diminution.

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