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Floral structure and development in Rafflesiaceae with emphasis on their exceptional gynoecia
Author(s) -
Nikolov Lachezar A.,
Staedler Yannick M.,
Manickam Sugumaran,
Schönenberger Jürg,
Endress Peter K.,
Kramer Elena M.,
Davis Charles C.
Publication year - 2014
Publication title -
american journal of botany
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.218
H-Index - 151
eISSN - 1537-2197
pISSN - 0002-9122
DOI - 10.3732/ajb.1400009
Subject(s) - gynoecium , biology , apex (geometry) , synapomorphy , botany , shoot , anatomy , stamen , phylogenetics , gene , pollen , clade , biochemistry
• Premise of the study: The holoparasitic plant family Rafflesiaceae include the world's largest flowers. Despite their iconic status, relatively little is known about the morphology and development of their flowers. A recent study clarified the organization of the outer (sterile) floral organs, surprisingly revealing that their distinctive floral chambers arose via different developmental pathways in the two major genera of the family. Here, we expand that research to investigate the structure and development of the reproductive organs of Rafflesiaceae. • Methods: Serial sectioning, scanning electron microscopy, and x‐ray tomography of floral buds were employed to reconstruct the structure and development of all three Rafflesiaceae genera. • Key results: Unlike most angiosperms, which form their shoot apex from the primary morphological surface, the shoot apex of Rafflesiaceae instead forms secondarily via internal cell separation (schizogeny) along the distal boundary of the host–parasite interface. Similarly, the radially directed ovarial clefts of the gynoecium forms via schizogeny within solid tissue, and no carpels are initiated from the floral apex. • Conclusions: The development of the shoot apex and gynoecium of Rafflesiaceae are highly unusual. Although secondary formation of the morphological surface from the shoot apex has been documented in other plant groups, secondary derivation of the inner gynoecium surface is otherwise unknown. Both features are likely synapomorphies of Rafflesiaceae. The secondary derivation of the shoot apex may protect the developing floral shoot as it emerges from within dense host tissue. The secondary formation of the ovarial clefts may generate the extensive placental area necessary to produce hundreds of thousands of ovules.

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