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Can a seed bank provide demographic and genetic rescue in a declining population of the endangered shrub Acacia pinguifolia?

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Abstract

Many threatened species suffer reduced genetic diversity as a result of small population size and isolation. However, species with a persistent seed bank may be buffered against genetic loss as seed banks are expected to accumulate the reproductive output of many seasons. For fire-dependent species in decline, prescribed ecological burning may be a means to stimulate germination and recover genetic diversity stored in the seed bank, providing a demographic and genetic rescue effect. Here we investigated the effectiveness of this strategy in a small, isolated and inbred population of the endangered shrub, Acacia pinguifolia. We surveyed genetic diversity and structure of remnant populations of A. pinguifolia and monitored regeneration before and after burning. Germination was stimulated by fire, but seedling numbers 18 months post-fire were low and barely above the number of adults killed by the fire. Genetic diversity was marginally higher in the post-fire seedling cohort than the pre-fire adults (HE = 0.1 vs. 0.09, respectively). Outcrossing rates of open-pollinated seed from surrounding plants suggested moderately high levels of self-fertilisation (t m  = 0.65) and analysis of fine-scale genetic structure implied pollen and seed dispersal over distances of several metres, suggesting that restricted gene flow and inbreeding may act to limit genetic diversity in the seed bank. We conclude that prescribed burning has not been immediately successful as a recovery strategy for this relictual population of A. pinguifolia, though future monitoring may detect additional recruits. Alternative conservation strategies, including performing inter-population crosses, may be required to restore genetic diversity and ameliorate extinction risks.

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References

  • Armbruster P, Reed DH (2005) Inbreeding depression in benign and stressful environments. Heredity 95:235–242

    Article  PubMed  CAS  Google Scholar 

  • Ecological Associates (2007) Eyre Peninsula bushfire recovery program vegetation monitoring. Department for Environment and Heritage, Port Lincoln, South Australia

  • Auld TD (2006) Population dynamics of the shrub Acacia suaveolens (Sm.) Willd.: dispersal and the dynamics of the soil seed-bank. Aust J Ecol 11:235–254

    Google Scholar 

  • Auld TD, Denham AJ (2006) How much seed remains in the soil after a fire? Plant Ecol 187:15–24

    Article  Google Scholar 

  • Bossuyt B (2007) Genetic rescue in an isolated metapopulation of a naturally fragmented plant species, Parnassia palustris. Conserv Biol 21:832–841

    Article  PubMed  Google Scholar 

  • Bradstock RA (2008) Effects of large fires on biodiversity in south-eastern Australia: disaster or template for diversity? Int J Wildland Fire 17:809–822

    Article  Google Scholar 

  • Bradstock RA, Auld TD (1995) Soil temperatures during experimental bushfires in relation to fire intensity—consequences for legume germination and fire management in south-eastern Australia. J Appl Ecol 32:76–84

    Article  Google Scholar 

  • Bradstock RA, Bedward M, Kenny BJ, Scott J (1998) Spatially-explicit simulation of the effect of prescribed burning on fire regimes and plant extinctions in shrublands typical of south-eastern Australia. Biol Conserv 86:83–95

    Article  Google Scholar 

  • Broadhurst LM, Lowe A, Coates DJ, Cunningham SA, Mc Donald M, Vesk PA, Yates C (2008) Seed supply for broadscale restoration: maximizing evolutionary potential. Evol Appl 1:587–597

    Google Scholar 

  • Brownlie H, Playford J, Wallace H, Shapcott A (2009) Population ecology and genetics of the vulnerable Acacia attenuata (Mimosaceae) and their significance for its conservation, recovery and translocation. Aust J Bot 57:675–687

    Article  Google Scholar 

  • Byers DL, Waller DM (1999) Do plant populations purge their genetic load? Effects of population size and mating history on inbreeding depression. Annu Rev Ecol Syst 30:479–514

    Article  Google Scholar 

  • Caughley G (1994) Directions in conservation biology. J Anim Ecol 63:215–244

    Article  Google Scholar 

  • Charlesworth D, Charlesworth B (1987) Inbreeding depression and its evolutionary consequences. Annu Rev Ecol Evol S 18:237–268

    Article  Google Scholar 

  • Coates DJ, Tischler G, McComb JA (2006) Genetic variation and the mating system in the rare Acacia sciophanes compared with its common sister species Acacia anfractuosa (Mimosaceae). Conserv Genet 7:931–944

    Article  Google Scholar 

  • Dolan RW, Quintana-Ascencio PF, Menges ES (2008) Genetic change following fire in populations of a seed-banking perennial plant. Oecologia 158:355–360

    Article  PubMed  Google Scholar 

  • Ellstrand NC, Elam DR (1993) Population genetic consequences of small population size—implications for plant conservation. Annu Rev Ecol Syst 24:217–242

    Article  Google Scholar 

  • Environmental and Biodiversity Services (2009) Prescribed burning as a management tool to stimulate the regeneration of the nationally endangered shrub Acacia pinguifolia (Fat-leaf Wattle). Final Report to Native Vegetation Research Fund, Adelaide

  • Farrell TP, Ashton DH (1978) Population studies on Acacia melanoxylon R. Br. I. Variation in seed and vegetative characteristics. Aust J Bot 26:365–379

    Article  Google Scholar 

  • Hardner CM, Potts BM, Gore PL (1998) The relationship between cross success and spatial proximity of Eucalyptus globulus ssp. globulus parents. Evolution 52:614–618

    Article  Google Scholar 

  • Hedrick PW, Kalinowski ST (2000) Inbreeding depression in conservation biology. Annu Rev Ecol Evol Syst 31:139–162

    Article  Google Scholar 

  • Hock Z, Szovenyi P, Schneller JJ, Toth Z, Urmi E (2008) Bryophyte diaspore bank: a genetic memory? Genetic structure and genetic diversity of surface populations and diaspore bank in the liverwort Mannia fragrans (Aytoniaceae). Am J Bot 95:542–548

    Article  CAS  Google Scholar 

  • Honnay O, Bossuyt B, Jacquemyn H, Shimono A, Uchiyama K (2008) Can a seed bank maintain the genetic variation in the above ground plant population? Oikos 117:1–5

    Article  Google Scholar 

  • Hufford KM, Mazer SJ (2003) Plant ecotypes: genetic differentiation in the age of ecological restoration. Trends Ecol Evol 18:147–155

    Article  Google Scholar 

  • Jessop JP, Toelken H (1986) Flora of South Australia. South Australian Government Printing Division, Adelaide

    Google Scholar 

  • Jusaitis M, Sorensen B (1994) Conservation studies on endangered plant species from South Australia’s agricultural regions. Black Hill Flora Centre, Adelaide, South Australia

    Google Scholar 

  • Lande R, Schemske DW, Schultz ST (1994) High inbreeding depression, selective interference among loci, and the threshold selfing rate for purging recessive lethal mutations. Evolution 48:965–978

    Article  Google Scholar 

  • Leimu R, Mutikainen P, Koricheva J, Fischer M (2006) How general are positive relationships between plant population size, fitness and genetic variation? J Ecol 94:942–952

    Article  Google Scholar 

  • Newman D, Tallmon DA (2001) Experimental evidence for beneficial fitness effects of gene flow in recently isolated populations. Conserv Biol 15:1054–1063

    Article  Google Scholar 

  • Obst C (2005) South Australian Murray Darling Basin threatened flora recovery plan. Report to the Threatened Species and Communities section, Australian Government Department of the Environment and Heritage, Canberra

  • Ooi MKJ, Auld TD, Whelan RJ (2004) Delayed post-fire seedling emergence linked to season: a case study with Leucopogon species (Epacridaceae). Plant Ecol 174:183–196

    Article  Google Scholar 

  • Orchard A, Wilson A (2001) Mimosaceae, Acacia part 2. ABRS/CSIRO Publishing, Melbourne

    Google Scholar 

  • Ouborg NJ, Vergeer P, Mix C (2006) The rough edges of the conservation genetics paradigm for plants. J Ecol 94:1233–1248

    Article  Google Scholar 

  • Outcalt KW, Brockway DG (2010) Structure and composition changes following restoration treatments of longleaf pine forests on the Gulf Coastal Plain of Alabama. For Ecol Manage 259:1615–1623

    Article  Google Scholar 

  • Peakall R, Smouse PE (2006) GenAlEx 6: Genetic analysis in Excel. Population genetic software for teaching and research. Mol Ecol Notes 6:288–295

    Article  Google Scholar 

  • Penman TD, Towerton AL (2008) Soil temperatures during autumn prescribed burning: implications for the germination of fire responsive species? Int J Wildland Fire 17:572–578

    Article  Google Scholar 

  • Pobke K (2007) Draft recovery plan for 23 threatened flora taxa on Eyre Peninsula, South Australia 2007–2012. Department for Environment and Heritage, Adelaide, South Australia

    Google Scholar 

  • Reed DH (2005) Relationship between population size and fitness. Conserv Biol 19:563–568

    Article  Google Scholar 

  • Reed DH, Frankham R (2003) Correlation between fitness and genetic diversity. Conserv Biol 17(1):230–237

    Article  Google Scholar 

  • Richardson DM, Kluge RL (2008) Seed banks of invasive Australian Acacia species in South Africa: role in invasiveness and options for management. Perspect Plant Ecol Evol Syst 10:161–177

    Article  Google Scholar 

  • Ritland K (2002) Extensions of models for the estimation of mating systems using n independent loci. Heredity 88:221–228

    Article  PubMed  Google Scholar 

  • Sabiiti EN, Wein RW (1987) Fire and Acacia seeds—a hypothesis of colonization success. J Ecol 75:937–946

    Article  Google Scholar 

  • Stone GN, Raine NE, Prescott M, Willmer PG (2003) Pollination ecology of acacias (Fabaceae, Mimosoideae). Aust Syst Bot 16:103–118

    Article  Google Scholar 

  • Storfer A (1999) Gene flow and endangered species translocations: a topic revisited. Biol Conserv 87:173–180

    Article  Google Scholar 

  • Templeton AR, Levin DA (1979) Evolutionary consequences of seed pools. Am Nat 114:232–249

    Article  Google Scholar 

  • Vos P, Hogers R, Bleeker M, Reijans M, van de Lee T, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M, Zabeau M (1995) AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414

    Article  PubMed  CAS  Google Scholar 

  • Wang JL (2004) Application of the one-migrant-per-generation rule to conservation and management. Conserv Biol 18:332–343

    Article  Google Scholar 

  • Willi Y, Van Kleunen M, Dietrich S, Fischer M (2007) Genetic rescue persists beyond first-generation outbreeding in small populations of a rare plant. Proc R Soc B-Biol Sci 274:2357–2364

    Article  Google Scholar 

  • Yates CJ, Broadhurst LM (2002) Assessing limitations on population growth in two critically endangered Acacia taxa. Biol Conserv 108:13–26

    Article  Google Scholar 

  • Young A, Boyle T, Brown T (1996) The population genetic consequences of habitat fragmentation for plants. Trends Ecol Evol 11:413–418

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We are indebted to Chris Obst (Environmental Biodiversity Services) for preparing, organising and managing the prescribed burn at Finniss. We thank Lynton Arney for access to the SteamRanger population and to the Department for Environment and Heritage and the Country Fire Service fire crews for conducting the prescribed burn. We are grateful to Kylie Moritz, Jo Spencer and Tanja Chapman for their help with monitoring and data analysis, and to Phil Ainsley and Manfred Jusaitis for their expert advice and discussion on this manuscript. We are also grateful to two anonymous reviewers whose comments improved this manuscript. Finally, we would also like to thank Katrina Pobke, Ben White and Louisa Halliday for providing Eyre Peninsula A. pinguifolia leaf material. This work was financially supported by a Native Vegetation Council Grant to K. Ottewell, D. Bickerton and C. Obst.

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Correspondence to Kym M. Ottewell.

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Ottewell, K.M., Bickerton, D. & Lowe, A.J. Can a seed bank provide demographic and genetic rescue in a declining population of the endangered shrub Acacia pinguifolia?. Conserv Genet 12, 669–678 (2011). https://doi.org/10.1007/s10592-010-0173-x

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