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Australian Journal of Botany Australian Journal of Botany Society
Southern hemisphere botanical ecosystems
RESEARCH ARTICLE

Female and male costs of reproduction must be equal in dioecious Cape plant genus Leucadendron (Proteaceae)

Jeremy J. Midgley A B , Adam G. West A and Michael D. Cramer A
+ Author Affiliations
- Author Affiliations

A Department of Biological Sciences, University of Cape Town, P bag Rondebosch, 7701, South Africa.

B Corresponding author. Email: Jeremy.Midgley@uct.ac.za

Australian Journal of Botany 67(7) 517-520 https://doi.org/10.1071/BT18170
Submitted: 28 August 2018  Accepted: 11 October 2019   Published: 20 December 2019

Abstract

The Cape Leucadendron genus is dioecious, with extreme vegetative dimorphism displayed in some species – females having much larger leaves and fewer branches than males – whereas other species are monomorphic. Leucadendron is ecologically diverse, with some species with canopy stored seeds (serotiny) and others with soil stored seeds. These features mean that the Cape Leucadendron is an ideal genus to study the costs of reproduction for the different sexes in plants, and to determine whether vegetative dimorphism could be due to unequal costs. Here we use the unique aspects of the fire-prone Cape environment in which leucadendrons occur to show that the costs of sex must be equal between the sexes. Leucadendron populations are single aged because they only recruit after fires that kill all adults. Therefore, because the sexes have the same lifespans, they must have the same lifetime extent of vegetative versus reproductive allocation. Also, ecologically similar hermaphrodite Proteaceae co-exist with dioecious taxa. To co-occur, dioecious and hermaphrodite taxa must have the same mean post-fire fitness. This implies that dioecious females must have double the reproductive output that a co-occurring hermaphrodite has. This is only possible if the costs of reproduction are the same for the sexes and that the sexes use the same resources for reproduction. Finally, because males and female co-occur, they must be competitively equivalent to maintain natal sex ratios. These three factors suggest male and female allocate equivalently and therefore that vegetative sexual dimorphism is unlikely to be due to differences in allocation.

Additional keywords: dioecy, Leucadendron, maternal costs, paternal costs, Proteaceae, serotiny, sexual allocation, vegetative dimorphism.


References

Barrett SCH, Hough J (2013) Sexual dimorphism in flowering plants. Journal of Experimental Biology 64, 67–82.

Hamilton WD (1967) Extraordinary sex ratios. Science 156, 477–488.
Extraordinary sex ratios.Crossref | GoogleScholarGoogle Scholar | 6021675PubMed |

Harris MS, Pannell JR (2010) Canopy seed storage is associated with sexual dimorphism in the woody dioecious genus Leucadendron. Journal of Ecology 98, 509–515.
Canopy seed storage is associated with sexual dimorphism in the woody dioecious genus Leucadendron.Crossref | GoogleScholarGoogle Scholar |

Hultine KR, Grady KC, Wood TE, Shuster SM, Stella JC, Whitham TG (2016) Climate change perils for dioecious plant species. Nature Plants 2, 16109
Climate change perils for dioecious plant species.Crossref | GoogleScholarGoogle Scholar | 28221374PubMed |

Laurie H, Mustart PJ, Cowling RM (1997) A shared niche? The case of the species pair Protea obtusifolia–Leucadendron meridianum. Oikos 79, 127–136.
A shared niche? The case of the species pair Protea obtusifolia–Leucadendron meridianum.Crossref | GoogleScholarGoogle Scholar |

Midgley JJ (2010) Causes of secondary sexual differences in plants – evidence from extreme leaf dimorphism in Leucadendron (Proteaceae). South African Journal of Botany 76, 588–592.
Causes of secondary sexual differences in plants – evidence from extreme leaf dimorphism in Leucadendron (Proteaceae).Crossref | GoogleScholarGoogle Scholar |

Mustart PJ, Cowling RM, Dunne TT (1994) Reproductive traits of two closely related species-pairs on adjacent, different soil types in South African Fynbos. Vegetatio 111, 161–171.
Reproductive traits of two closely related species-pairs on adjacent, different soil types in South African Fynbos.Crossref | GoogleScholarGoogle Scholar |

Roddy AB, van Blerk JJ, Midgley JJ, West AG (2019) Ramification has little impact on shoot hydraulic efficiency in the sexually dimorphic genus Leucadendron (Proteaceae). PeerJ 7, e6835
Ramification has little impact on shoot hydraulic efficiency in the sexually dimorphic genus Leucadendron (Proteaceae).Crossref | GoogleScholarGoogle Scholar | 31179169PubMed |

Schmeisser M, Steyn WJ, Jacobs G (2010) Regreening of involucral leaves of female Leucadendron (Proteaceae) after flowering. Australian Journal of Botany 58, 586–596.
Regreening of involucral leaves of female Leucadendron (Proteaceae) after flowering.Crossref | GoogleScholarGoogle Scholar |

Williams IJM (1972) The genus Leucadendron (Proteaceae). Contributions of Bolus Herbarium 3, 1–425.