Floral anatomy, embryology, seed, and fruit development in Cephalanthus (Naucleeae-Rubiaceae), with emphasis on C. glabratus
- PMID: 33990859
- DOI: 10.1007/s00709-021-01664-8
Floral anatomy, embryology, seed, and fruit development in Cephalanthus (Naucleeae-Rubiaceae), with emphasis on C. glabratus
Abstract
Information on the reproductive anatomy in genera of the tribe Naucleeae, particularly Cephalanthus, is scarce and fragmented. Of the six species in the genus, only the mature megagamethophyte of Cephalanthus occidentalis has been described. This study aims to provide information on embryological aspects in flowers of C. glabratus and to analyze the morphology and anatomy of the flowers, fruit, and seed in the six species of the genus. Cephalanthus glabratus have imperfect flowers: pistillate (PF) and staminate (SF). In the PF, the ovules are functional, while in the SF, they atrophy during the formation of the embryo sac. The mature ovule has a single integument, corresponds to the Phyllis type and the embryo sac is a Polygonum type, forming only in the PF. The presence of pollenkitt and secondary presentation of pollen were observed in the SF, as well as in the pollen formation previously described, whereas in the PF, they are absent, due to the collapse of the pollen grains inside the indehiscent anthers. The analysis of the ontogeny of the ovular excrescence in C. glabratus determined its funicular origin, calling it an aril. Its development is a pre-anthesis event, initiated during megasporogenesis. In seeds, the aril is a fleshy, white appendage which almost completely envelops the seeds of Cephalanthus, except for Cephalanthus natalensis where it is noticeably more reduced. Studies of the fruit in Cephalanthus species indicate that the infructescence is a dry schizocarp which separates into uni-seminated mericarps, except in C. natalensis that has fleshy indehiscent fruit.
Keywords: Aril; Embryology; Fruit; Imperfect flowers; Naucleeae.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.
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References
-
- Andronova NN (1977) On the structure of the ovule of Rubiaceae. Bot Zeitg 62:1461–1469
-
- Arbo MM, Gonzalez AM, Sede SM (2015) Phylogenetic relationship within Turneraceae based on morphological characters with emphasis on seed micromorphology. Plant Syst Evol 301(7):1907–1926
-
- Bacigalupo NM (1974) Rubiaceae. In: Burkart AE (ed) Flora Ilustrada de Entre Ríos, vol. 6 (6). Colección Científica del INTA, Buenos Aires, p 3–50
-
- Bahadur B (1968) Heterostyly in Rubiaceae: a review. Osmania Univ J Sci [Golden Jubilee Vol.] 4(1/2): 207–238. [p. 123, 124]
-
- Bell G (2008) Selection: the mechanism of evolution. Oxford University Press
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