Perianth symmetry in sexually differentiated flowers of Akebia quinata (Lardizabalaceae)
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
40980069
PubMed Central
PMC12449860
DOI
10.7717/peerj.20060
PII: 20060
Knihovny.cz E-zdroje
- Klíčová slova
- Actinomorphy, Akebia, Floral biology, Geometric morphometrics, Monoecy, Triradial symmetry,
- MeSH
- květy * anatomie a histologie růst a vývoj fyziologie MeSH
- opylení MeSH
- Publikační typ
- časopisecké články MeSH
Sexual differentiation of monoecious plants usually involves differentiation in the size of female and male flowers produced on the same individuals. In the nectarless Akebia quinata (Houtt.) Decne (Lardizabalaceae), the trimeric, actinomorphic female flowers are larger than the males, which is explained as an adaptive trait to prevent self-pollination, as conspicuous female flowers are usually visited by pollinators earlier than smaller male flowers of the same individuals. This results in the plants being cross-pollinated rather than geitonogamously pollinated. However, it is also known that the development of the perianth in this species is genetically associated with the ontogeny of the petaloid sepals. These are thus developmentally linked to the ontogeny of the stamens. Therefore, it is possible that female flowers lacking fertile stamens also have less developmental control over the perianth ontogeny. Consequently, our study investigated whether female and male flowers of A. quinata differ in their overall shape features, in the amounts of variation among flowers, as well as in the extent of different types of asymmetry in perianth shapes. Geometric morphometric analyses of triradial perianth symmetry based on the generalised Procrustes analysis of a complete symmetry group of perianth shapes showed that female flowers were indeed significantly more variable in all different subspaces of their symmetric and asymmetric shape variation. This included the differences among individual flowers, their rotational and bilateral symmetry as well as the asymmetry among sepals within flowers. These results indicate that developmental control over perianth shape is systematically weaker in female flowers compared to male flowers of A. quinata. It is therefore likely that this phenomenon is related to the presence or absence of fertile male reproductive organs, whose development is linked to the ontogeny of the perianth and the maintenance of its trimeric symmetry.
Czech Botanical Society Prague Czech Republic
Department of Botany Faculty of Science Charles University Prague Prague Czech Republic
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Adams DC, Otárola-Castillo E. geomorph: an R package for the collection and analysis of geometric morphometric shape data. Methods in Ecology and Evolution. 2013;4:393–399. doi: 10.1111/2041-210X.12035. DOI
Barrett SCH, Hough J. Sexual dimorphism in flowering plants. Journal of Experimental Botany. 2013;64:67–82. doi: 10.1093/jxb/ers308. PubMed DOI
Bell G. On the function of flowers. Proceedings of the Royal Society B: Biological Sciences. 1985;224:223–265. doi: 10.1098/rspb.1985.0031. DOI
Berger BA, Ricigliano VA, Savriama Y, Lim A, Thompson V, Howarth DG. Geometric morphometrics reveals shifts in flower shape symmetry and size following gene knockdown of Cycloidea and Anthocyanidin synthase. BMC Plant Biology. 2017;17:205. doi: 10.1186/s12870-017-1152-x. PubMed DOI PMC
Bookstein FL. A course in morphometrics for biologists. Cambridge University Press; Cambridge: 2018.
Budečević S, Manitašević Jovanović S, Vuleta A, Tucić B, Klingenberg CP. Directional asymmetry and direction-giving factors: lessons from flowers with complex symmetry. Evolution & Development. 2022;24:92–108. doi: 10.1111/ede.12402. PubMed DOI PMC
Carrive L, Domenech B, Sauquet H, Jabbour F, Damerval C, Nadot S. Insights into the ancestral flowers of Ranunculales. Botanical Journal of the Linnean Society. 2020;194:23–46. doi: 10.1093/botlinnean/boaa031. DOI
Chanderbali AS, Berger BA, Howarth DG, Soltis PS, Soltis DE. Evolving ideas on the origin and evolution of flowers: new perspectives in the genomic era. Genetics. 2016;202:1255–1265. doi: 10.1534/genetics.115.182964. PubMed DOI PMC
Christenhusz MJM. An overview of Lardizabalaceae. Curtis’s Botanical Magazine. 2012;29:235–276. doi: 10.1111/j.1467-8748.2012.01790.x. DOI
Christenhusz MJM, Rix M. Akebia quinata. Curtis’s Botanical Magazine. 2012;29:284–289. doi: 10.1111/j.1467-8748.2012.01792.x. DOI
Cronk Q. The distribution of sexual function in the flowering plant: from monoecy to dioecy. Philosophical Transactions of the Royal Society B: Biological Sciences. 2022;377:20210486. doi: 10.1098/rstb.2021.0486. PubMed DOI PMC
Delph LF. Flower size dimorphism in plants with unisexual flowers. In: Lloyd DG, Barrett SCH, editors. Floral biology. Chapman & Hall; New York: 1996. pp. 217–240. DOI
Delph LF, Galloway LF, Stanton ML. Sexual dimorphism in flower size. The American Naturalist. 1996;148:299–320. doi: 10.1086/285926. DOI
Delph LF, Touzet P, Bailey MF. Merging theory and mechanism in studies of gynodioecy. Trends in Ecology and Evolution. 2007;22:17–24. doi: 10.1016/j.tree.2006.09.013. PubMed DOI
Eckhart VM. Sexual dimorphism in flowers and inflorescences. In: Geber MA, Dawson TE, Delph LF, editors. Gender and sexual dimorphism in flowering plants. Springer; Heidelberg: 1999. pp. 123–148. DOI
Frey FM, Bukoski M. Floral symmetry is associated with flower size and pollen production but not insect visitation rates in Geranium robertianum (Geraniaceae) Plant Species Biology. 2014;29:272–280. doi: 10.1111/1442-1984.12021. DOI
Glasnović P, FišerPečnikar Ž. Akebia quinata (Houtt.) Dcne., new species for Slovenian flora, and contribution to the knowledge of the neophytic flora of Primorska region. Hladnikia. 2010;25:31–43.
Gómez JM, Perfectti F. Evolution of complex traits: the case of Erysimum corolla shape. International Journal of Plant Sciences. 2010;171:987–998. doi: 10.1086/656475. DOI
Hammer Ø, Harper DAT, Ryan PD. PAST: paleontological statistics software package for education and data analysis. Palaeontologia Electronica. 2001;4:1–9.
Karasawa MMG. Reproductive diversity of plants. Springer International Publishing; Cham: 2015.
Kawagoe T, Suzuki N. Floral sexual dimorphism and flower choice by pollinators in a nectarless monoecious vine Akebia quinata (Lardizabalaceae) Ecological Research. 2002;17:295–303. doi: 10.1046/j.1440-1703.2002.00489.x. DOI
Kawagoe T, Suzuki N. Flower-size dimorphism avoids geitonogamous pollination in a nectarless monoecious plant Akebia quinata. International Journal of Plant Sciences. 2003;164:893–897. doi: 10.1086/378659. DOI
Kawagoe T, Suzuki N. Self-pollen on a stigma interferes with outcrossed seed production in a self-incompatible monoecious plant, Akebia quinata (Lardizabalaceae) Functional Ecology. 2005;19:49–54. doi: 10.1111/j.0269-8463.2005.00950.x. DOI
Klingenberg CP. Analyzing fluctuating asymmetry with geometric morphometrics: concepts, methods, and applications. Symmetry. 2015;7:843–934. doi: 10.3390/sym7020843. DOI
Møller AP, Eriksson M. Pollinator preference for symmetrical flowers and sexual selection in plants. Oikos. 1995;73:15–22. doi: 10.2307/3545720. DOI
Møller AP, Sorci G. Insect preference for symmetrical artificial flowers. Oecologia. 1998;114:37–42. doi: 10.1007/s004420050417. PubMed DOI
Neustupa J. Gynodioecy in the common spindle tree (Euonymus europaeus L.) involves differences in the asymmetry of corolla shapes between sexually differentiated flowers. PeerJ. 2020;8:e8571. doi: 10.7717/peerj.8571. PubMed DOI PMC
Neustupa J, Woodard K. Male sterility significantly elevates shape variation and fluctuating asymmetry of zygomorphic corolla in gynodioecious Glechoma hederacea (Lamiaceae) AoB Plants. 2021;13:plab013. doi: 10.1093/aobpla/plab013. PubMed DOI PMC
Payne WW, Seago JL. The open conduplicate carpel of Akebia quinata (Berberidales: Lardizabalaceae) American Journal of Botany. 1968;55:575–581. doi: 10.1002/j.1537-2197.1968.tb07414.x. DOI
Portmann A. Neue Wege der Biologie. R. Piper & Co Verlag; München: 1960.
R Development Core Team R: a language and environment for statistical computing. https://cran.r-project.org/bin/windows/base/old/4.4.1/ [29 March 2025];2024
Renner SS. The relative and absolute frequencies of angiosperm sexual systems: dioecy, monoecy, gynodioecy, and an updated online database. American Journal of Botany. 2014;101:1588–1596. doi: 10.3732/ajb.1400196. PubMed DOI
Rohlf FJ. The tps series of software. Hystrix Italian Journal of Mammalogy. 2015;26:912. doi: 10.4404/hystrix-26.1-11264. DOI
Savriama Y. A step-by-step guide for geometric morphometrics of floral symmetry. Frontiers in Plant Science. 2018;9:1433. doi: 10.3389/fpls.2018.01433. PubMed DOI PMC
Savriama Y, Gerber S. Geometric morphometrics of nested symmetries unravels hierarchical inter- and intra-individual variation in biological shapes. Scientific Reports. 2018;8:18055. doi: 10.1038/s41598-018-36147-z. PubMed DOI PMC
Savriama Y, Klingenberg CP. Beyond bilateral symmetry: geometric morphometric methods for any type of symmetry. BMC Evolutionary Biology. 2011;11:280. doi: 10.1186/1471-2148-11-280. PubMed DOI PMC
Savriama Y, Neustupa J, Klingenberg CP. Geometric morphometrics of symmetry and allometry in Micrasterias rotata (Zygnematophyceae, Viridiplantae) Nova Hedwigia Beihefte. 2010;136:43–54. doi: 10.1127/1438. DOI
Schaefer K, Lauc T, Mitteroecker P, Gunz P, Bookstein FL. Dental arch asymmetry in an isolated Adriatic community. American Journal of Physical Anthropology. 2006;129:132–142. doi: 10.1002/ajpa.20224. PubMed DOI
Shan H, Su K, Lu W, Kong H, Chen Z, Meng Z. Conservation and divergence of candidate class B genes in Akebia trifoliata (Lardizabalaceae) Development, Genes and Evolution. 2006;216:785–795. doi: 10.1007/s00427-006-0107-2. PubMed DOI
Sobral R, Costa MMR. Role of floral organ identity genes in the development of unisexual flowers of Quercus suber L. Scientific Reports. 2017;7:10368. doi: 10.1038/s41598-017-10732-0. PubMed DOI PMC
Tucić B, Budečević S, Manitašević Jovanović S, Vuleta A, Klingenberg CP. Phenotypic plasticity in response to environmental heterogeneity contributes to fluctuating asymmetry in plants: first empirical evidence. Journal of Evolutionary Biology. 2018;31:197–210. doi: 10.1111/jeb.13207. PubMed DOI
Wang C, Zou T, Liu W, Wang X. The influence of self-pollen deposition on female reproductive success in a self-incompatible plant, Akebia quinata. Frontiers in Plant Science. 2022;13:935217. doi: 10.3389/fpls.2022.935217. PubMed DOI PMC
Zhang X, Pan L, Guo W, Li Y, Wang W. A convergent mechanism of sex determination in dioecious plants: distinct sex-determining genes display converged regulation on floral B-class genes. Frontiers in Plant Science. 2022;13:953445. doi: 10.3389/fpls.2022.953445. PubMed DOI PMC
Zhang X, Ren Y. Comparative floral development in Lardizabalaceae (Ranunculales) Botanical Journal of the Linnean Society. 2011;166:171–184. doi: 10.1111/j.1095-8339.2011.01144.x. DOI