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

Fire intensity, serotiny and seed release in 19 woody species: evidence for risk spreading among wind-dispersed and resprouting syndromes

Peter J. Clarke A B , Kirsten J. E. Knox A and Damian Butler A
+ Author Affiliations
- Author Affiliations

A Department of Botany, School of Environmental and Rural Science, University of New England, Armidale, NSW, 2351 Australia.

B Corresponding author. Email: pclarke1@une.edu.au

Australian Journal of Botany 58(8) 629-636 https://doi.org/10.1071/BT10193
Submitted: 2 August 2010  Accepted: 13 October 2010   Published: 9 December 2010

Abstract

Seed storage in woody fruits on plants has been much studied, whereas trait variation in seed release has been given scant attention. In non-Mediterranean climates, some species release seeds immediately after fire, whereas others retain seeds in open fruits/cones for longer. We expected that species with wind-dispersed seeds and those killed by fire would spread their recruitment risks by having stronger cues for fruit opening and slower seed release once fruits were open. We therefore tested whether fire intensity (heat) affected fruit opening and seed release in 19 species. We then contrasted fruit opening and seed release among (1) serotiny levels (weak, moderate, strong), (2) dispersal (wind v. unassisted) and (3) resprouting ability (killed v. resprout) traits. Only three species required heat for fruit opening. Most species, however, retained varying proportions of seeds in open fruits. Strongly and moderately serotinous species retained seeds in open fruits longer than did weakly serotinous species. Both species with wind-dispersed seeds and fire-killed species required stronger heat effects for fruits to open but retained seeds in open fruits longer than did species with alternative traits. By delaying seed release after fruits have opened, species with wind-dispersed seeds, and those that are killed by fire, maximise the ability of seeds to arrive at safe sites after fire.


References

Allen R, Wardrop AB (1964) The opening and shedding mechanism of the female cones on Pinus radiata. Australian Journal of Botany 12, 125–134.
The opening and shedding mechanism of the female cones on Pinus radiata.Crossref | GoogleScholarGoogle Scholar |

Bond WJ (1985) Canopy-stored seed reserves (serotiny) in Cape Proteaceae. South African Journal of Botany 51, 181–186.

Bond WJ, van Wilgen BW (1996) ‘Fire and plants.’ (Chapman and Hall: London)

Bradstock RA, Myerscough PJ (1981) Fire effects on seed release and the emergence and establishment of seedlings in Banksia ericifolia L. Australian Journal of Botany 29, 521–531.
Fire effects on seed release and the emergence and establishment of seedlings in Banksia ericifolia L.Crossref | GoogleScholarGoogle Scholar |

Cowling RM, Lamont BB (1985) Seed release in Banksia: the role of wet–dry cycles. Australian Journal of Ecology 10, 169–171.
Seed release in Banksia: the role of wet–dry cycles.Crossref | GoogleScholarGoogle Scholar |

Cowling RM, Lamont BB (1987) Post-fire recruitment of four co-occurring Banksia species. Journal of Applied Ecology 24, 645–658.
Post-fire recruitment of four co-occurring Banksia species.Crossref | GoogleScholarGoogle Scholar |

Cramer MD, Midgley JJ (2009) Maintenance costs of serotiny do not explain weak serotiny. Austral Ecology 34, 653–662.
Maintenance costs of serotiny do not explain weak serotiny.Crossref | GoogleScholarGoogle Scholar |

Enright NJ, Lamont BB (1989a) Seed banks, fire season, safe sites and seedling recruitment in five co-occurring Banksia species. Journal of Ecology 77, 1111–1122.
Seed banks, fire season, safe sites and seedling recruitment in five co-occurring Banksia species.Crossref | GoogleScholarGoogle Scholar |

Enright NJ, Lamont BB (1989b) Fire temperatures and follicle-opening requirements in ten Banksia species. Australian Journal of Ecology 14, 107–113.
Fire temperatures and follicle-opening requirements in ten Banksia species.Crossref | GoogleScholarGoogle Scholar |

Enright NJ, Mosner E, Miller BP, Johnson N, Lamont BB (2007) Soil vs. canopy seed storage and plant species coexistence in species-rich Australian shrublands. Ecology 80, 2292–2304.

Garcillán PP (2010) Seed release without fire in Callitropsis guadalupensis, a serotinous cypress of a Mediterranean-climate oceanic island. Journal of Arid Environments 74, 512–515.
Seed release without fire in Callitropsis guadalupensis, a serotinous cypress of a Mediterranean-climate oceanic island.Crossref | GoogleScholarGoogle Scholar |

Gill AM (1981) Adaptive responses of Australian vascular plant species to fires. In ‘Fire and the Australian biota’. (Eds AM Gill, RH Groves, IR Noble) pp. 243–271. (Australian Academy of Science: Canberra)

Keeley KE, Zedler PH (1998) Life history evolution in pines. In ‘Ecology and biogeography of Pinus’. (Ed. DM Richardson) pp. 219–249. (Cambridge University Press: Cambridge, UK)

Knox KJE, Clarke PJ (2006) Fire season and intensity affect shrub recruitment in temperate sclerophyllous woodlands. Oecologia 149, 730–739.

Lamont BB (1988) Sexual versus vegetative reproduction in Banksia elegans. Botanical Gazette 149, 370–375.
Sexual versus vegetative reproduction in Banksia elegans.Crossref | GoogleScholarGoogle Scholar |

Lamont BB (1991) Canopy seed storage and release – what’s in a name? Oikos 60, 266–268.
Canopy seed storage and release – what’s in a name?Crossref | GoogleScholarGoogle Scholar |

Lamont BB, Barker MJ (1988) Seed bank dynamics of a serotinous, fire-sensitive Banksia species. Australian Journal of Botany 36, 193–203.
Seed bank dynamics of a serotinous, fire-sensitive Banksia species.Crossref | GoogleScholarGoogle Scholar |

Lamont BB, Le Maitre DC, Cowling RM, Enright NJ (1991) Canopy seed storage in woody plants. Botanical Review 57, 277–317.
Canopy seed storage in woody plants.Crossref | GoogleScholarGoogle Scholar |

Moya D, Saracino A, Salvatore R, Lovreglio R, de Las Heras J, Leone V (2008) Anatomic basis and insulation of serotinous cones in Pinus halepensis Mill. Trees 22, 511–519.
Anatomic basis and insulation of serotinous cones in Pinus halepensis Mill.Crossref | GoogleScholarGoogle Scholar |

Peters EM, Martorell C, Ezcurra E (2009) The adaptive value of cued seed dispersal in desert plants: seed retention and release in Mammillaria pectinifera, a small globose cactus. American Journal of Botany 96, 537–541.
The adaptive value of cued seed dispersal in desert plants: seed retention and release in Mammillaria pectinifera, a small globose cactus.Crossref | GoogleScholarGoogle Scholar |

Quinn GP, Keogh MJ (2002) ‘Experimental design and data analysis for biologists.’ (Cambridge University Press: Cambridge, UK)

Reyes O, Casal M (2002) Effect of high temperature on cone opening and on the release and viability of Pinus pinaster and Pinus radiata seeds in NW Spain. Annals of Forest Science 59, 327–334.
Effect of high temperature on cone opening and on the release and viability of Pinus pinaster and Pinus radiata seeds in NW Spain.Crossref | GoogleScholarGoogle Scholar |

Thanos CA (2004) Bradychory – The coining of a new term. In ‘Proceedings of the 10th MEDECOS conference, 25 April – 1 May, Rhodes, Greece’. pp. 1–6. (Millpress: Rotterdam, The Netherlands)

Whelan RJ, de Jong NH, Von der Burg S (1998) Variation in bradyspory and seedling recruitment without fire among populations of Banksias serrata (Proteaceae). Australian Journal of Ecology 23, 121–128.
Variation in bradyspory and seedling recruitment without fire among populations of Banksias serrata (Proteaceae).Crossref | GoogleScholarGoogle Scholar |

Zammit CA, Westoby M (1987) Seedling recruitment strategies in obligate-seeding and resprouting Banksia shrubs. Ecology 68, 1984–1992.
Seedling recruitment strategies in obligate-seeding and resprouting Banksia shrubs.Crossref | GoogleScholarGoogle Scholar |