The persistence niche: what makes it and what breaks it for two fire-prone plant species
David A. Keith A D , Mark G. Tozer A , Tracey J. Regan B and Helen M. Regan CA NSW Department of Environment and Conservation, PO Box 1967, Hurstville, NSW 2220, Australia.
B The Ecology Centre, University of Queensland, Brisbane, Qld 4071, Australia.
C Biology Department, San Diego State University, 5500 Campanile Drive, San Diego, CA 92 181-4614, USA.
D Corresponding author. Email: david.keith@environment.nsw.gov.au
Australian Journal of Botany 55(3) 273-279 https://doi.org/10.1071/BT06018
Submitted: 1 February 2006 Accepted: 10 July 2006 Published: 18 May 2007
Abstract
Persistence niches are expected to favour qualitatively different plant life histories compared with regeneration niches. In fire-prone habitats, for example, resprouting plants may be expected to exploit persistence niches, whereas obligate-seeders by definition exploit regeneration niches. Resprouter life histories should be typified by high rates of survival, which may be offset by relatively low rates of growth and reproduction. This combination of characters is expected to result from trade-offs in resource allocation and because the longevity of individual plants should buffer their populations against the effects of recruitment failure. We asked whether two resprouting perennial shrubs, Epacris barbata Melville and Xanthorrhoea resinifera (Sol. Ex Kite) E.C.Nelson & D.J.Bedford, exhibited the life-history character combinations that are expected for species exploiting a persistence niche. We also investigated how a change in habitat suitability caused by the invasion of a root pathogen may limit the ability of these species to occupy persistence niches. Demographic censuses of several years’ duration in two populations of each species yielded estimates of vital rates that were consistent with the life-history profile expected for a persistence niche. Rates of background survival were high and rates of fire-related mortality were low in both species. As expected, these were associated with low rates of growth and seedling establishment, although rates of seed production and viability were relatively high in both species. The importance of survival was confirmed by stochastic population models, which showed that population viability was more sensitive to decreases in survival of mature plants and increases in fire mortality of established plants than to changes in other vital rates. Seedling growth rates were also relatively important in E. barbata. Populations of both species that had been infected by root rot disease, Phytophthora cinnamomi, had substantially reduced survival rates and, consequently, reduced population viability. These effects were more extreme in E. barbata than in X. resinifera. We conclude that processes that reduce survival, such as disease infection and habitat loss, rather than processes that impede seed production and recruitment mediate the persistence niche. However, we discuss the possibility that this dependency might be mitigated by high fecundity if infrequent conditions that permit large recruitment events have so far eluded detection.
Acknowledgements
We thank the many technical staff and volunteers who assisted with plant censuses. We also thank Resit Akçakaya, Mark Burgman and Mick McCarthy for discussions that assisted development of the population models.
Auld TD, Denham AJ
(2001) The impact of seed predation by mammals on post-fire seed accumulation in the endangered Grevillea caleyi (Proteaceae). Biological Conservation 97, 377–385.
| Crossref | GoogleScholarGoogle Scholar |
Bellemare J,
Motzkin G, Foster DR
(2002) Legacies of the agricultural past in the forested present: an assessment of historical land-use effects on ricj mesic forests. Journal of Biogeography 29, 1401–1420.
| Crossref | GoogleScholarGoogle Scholar |
Bond WJ, Midgley JJ
(2001) Ecology of sprouting in woody plants: the persistence niche. Trends in Ecology and Evolution 16, 45–51.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Bradstock RA, Bedward M
(1992) Simulation of the effect of season of fire on post-fire seedling emergence of two Banksia species based on long-term rainfall records. Australian Journal of Botany 40, 75–88.
| Crossref | GoogleScholarGoogle Scholar |
Bradstock RA, O’Connell M
(1988) Demography of woody plants in relation to fire: Banksia ericifolia L.f. and Petrophile pulchella (Schrad) R.Br. Australian Journal of Ecology 13, 505–518.
| Crossref | GoogleScholarGoogle Scholar |
Burgman MA, Lamont BB
(1992) A stochastic model for the viability of Banksia cuneata populations: environmental, demographic and genetic effects. Jounral of Applied Ecology 29, 719–727.
| Crossref |
Cohn JS, Bradstock RA
(2000) Factors affecting post-fire seedling establishment of selected mallee understorey species. Australian Journal of Botany 48, 59–70.
| Crossref | GoogleScholarGoogle Scholar |
Dreschler M,
Lamont BB,
Burgman MA,
Akçakaya HR,
Witkowski ETF, Supriyadi
(1999) Modelling the persistence of an apparently immortal Banksia species after fire and land clearing. Biological Conservation 88, 249–259.
| Crossref | GoogleScholarGoogle Scholar |
Enright NJ,
Marsula R,
Lamont BB, Wissel C
(1998) The ecological significance of canopy seed storage in fire-prone environments: a model for resprouting shrubs. Journal of Ecology 86, 960–973.
| Crossref | GoogleScholarGoogle Scholar |
Eriksson O, Froberg H
(1996) ‘Windows of opportunity’ for recruitment in long-lived clonal plants: experimental studies of seedling establishment in Vaccinium shrubs. Canadian Journal of Botany 74, 1369–1374.
Garcia D, Zamora R
(2003) Persistence, multiple demographic strategies and conservation in long-lived Mediterranean plants. Journal of Vegetation Science 14, 921–926.
| Crossref | GoogleScholarGoogle Scholar |
Gill AM, Inwerson F
(1976) Growth of Xanthorrhoea australis R.Br. in relation to fire. Journal of Applied Ecology 13, 195–203.
| Crossref |
Grubb P
(1977) The maintenance of species richness in plant communities: the importance of the regeneration niche. Biological Review 52, 107–145.
Keith DA
(1996) Fire-driven mechanisms of extinction in vascular plants: a review of empirical and theoretical evidence in Australian vegetation. Proceedings of the Linnean Society of New South Wales 116, 37–78.
Keith DA
(1997) Combined effects of heat shock, smoke and darkness on germination of Epacris stuartii Stapf, an endangered fire-prone Australian shrub. Oecologia 112, 340–344.
| Crossref | GoogleScholarGoogle Scholar |
Keith DA
(2002) Population dynamics of an endangered heathland shrub, Epacris stuartii (Epacridaceae): recruitment, establishment and survival. Austral Ecology 27, 67–76.
| Crossref | GoogleScholarGoogle Scholar |
Leigh JH, Holgate A
(1979) The responses of the understorey of forests and woodlands of southern tablelands to grazing and burning. Australian Journal of Ecology 4, 25–45.
| Crossref | GoogleScholarGoogle Scholar |
McCarthy MA, Thompson C
(2001) Expected minimum population size as a measure of threat. Animal Conservation 4, 351–355.
| Crossref | GoogleScholarGoogle Scholar |
Noble IR, Slatyer RO
(1980) The use of vital attributes to predict successional changes in plant communities subject recurrent disturbances. Vegetatio 43, 5–21.
| Crossref | GoogleScholarGoogle Scholar |
O’Dowd D, Gill AM
(1984) Predator satiation and site alteration following fire: mass reproduction of alpine ash in south-eastern Australia. Ecology 65, 1052–1066.
| Crossref | GoogleScholarGoogle Scholar |
Shearer B, Dillon M
(1995) Susceptibility of plant species in Banksia woodlands on the Swan coastal plain, Western Australia, to infection by Phytophthora cinnamomi. Australian Journal of Botany 43, 113–134.
| Crossref | GoogleScholarGoogle Scholar |
Stearns SC
(1976) Life-history tactics: a review of the ideas. The Quarterly Review of Biology 51, 3–47.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Walsh JL,
Keith DA,
McDougall KL,
Summerell BA, Whelan RJ
(2006) Phytophthora root rot: assessing the potential threat to Australia’s oldest national park. Ecological Management and Restoration 7, 55–60.
| Crossref | GoogleScholarGoogle Scholar |
Warner RR, Chesson PL
(1985) Coexistence mediated by environmental variability: a field guide to the storage effect. American Naturalist 126, 769–787.