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Inbreeding depression in the partially self-incompatible endemic plant species Scalesia affinis (Asteraceae) from Galápagos islands

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Abstract

A previous study showed that some individuals of the tetraploid Galápagos endemic Scalesia affinis were able to produce offspring after selfing. The present study compares the fitness of self-pollinated offspring with the fitness of cross-pollinated offspring. Germination success, seedling survival, and four different growth parameters was measured. In most of the studied characters selfed offspring were significantly inferior to outcrossed progeny. The effect was very clear in germination and survival. Outcrossed embryos were 3.4 times more likely to germinate than those that were selfed-fertilized, and the mortality was 84% higher among selfed individuals. Also, there was no genetic variation in inbreeding depression. The present study is based on material from a large population on Isabela Island, Galápagos. At other localities in the archipelago, populations have been through recent dramatic bottlenecks due to the grazing of introduced mammals. Considering the significant inbreeding depression found in the large population and the presence of a partial self-incompatibility system, these small populations are likely to be highly vulnerable and their future survival critically threatened.

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References

  • Ågren J, Schemske DW (1993) Outcrossing rate and inbreeding depression in two annual monoecious herbs, Begonia hirsuta and B. semiovata. Evolution 47:125–135

    Article  Google Scholar 

  • Adsersen H (1989) The rare plants of the Galápagos Islands and their conservation. Biol Conserv 47:49–77

    Article  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • Byers DL, Meagher TR, (1992) Mate availability in small populations of plant species with homomorphic sporophytic self-incompatibility. Heredity 68:353–359

    Google Scholar 

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

    Article  Google Scholar 

  • Charlesworth B, Charlesworth D (1990) Inbreeding depression with heterozygote advantage and its effect on selection for modifiers changing the outcrossing rate Evolution 44:870–888

    Article  Google Scholar 

  • Cheptou PO (2006) The ecology of inbreeding depression. Heredity 96:110

    Article  PubMed  Google Scholar 

  • Culley TM, Weller SG, Sakai AK, Rankin AE (1999) Inbreeding depression and selfing rates in a self-compatible, hermaphroditic species, Schiedea membranacea (Caryophyllaceae). Am J Bot 86:980–987

    Article  PubMed  Google Scholar 

  • Darwin CR (1876) The effects of cross and self-fertilization in the vegetable kingdom. John Murray, London

    Google Scholar 

  • De Mauro MM (1993) Relationship of breeding system to rarity in the Lakeside Daisy (Hymenoxys acaulis var. glabra). Conserv Biol 7:542–550

    Article  Google Scholar 

  • Eliasson U (1974) Studies in Galápagos plants XIV. The genus Scalesia Arn. Opera Botanica 36:1–117

    Google Scholar 

  • Fischer M, Hock M, Paschke M (2003) Low genetic variation reduces cross-compatibility and offspring fitness in populations of a narrow endemic plant with a self-incompatibility system. Conserv Genet 4:325–336

    Article  CAS  Google Scholar 

  • Fishman L (2001) Inbreeding depression in two populations of Arenaria uniflora (Caryophyllaceae) with contrasting mating systems. Heredity 86:184–194

    Article  PubMed  CAS  Google Scholar 

  • Frankham R (1998) Inbreeding and extinction: Island populations. Conserv Biol 12:665–675

    Article  Google Scholar 

  • Frankham R, Briscoe DA, Ballou JD (2002) Introduction to conservation genetics. Cambridge University Press

  • Gigord L, Lavigne C, Shykoff JA (1998) Partial self-incompatibility and inbreeding depression in a native tree species of La Réunion (Indian Ocean). Oecologia 117:342–352

    Article  Google Scholar 

  • Hansen T (2003) Quantitative genetics of sexual allocation and inbreeding depression in hermaphroditic plants with special reference to Silene nutans (Caryophyllaceae). Ph.D. Dissertation, University of Copenhagen, p 47

  • Hilton-Taylor, C (compiler) (2000) 2000 IUCN Red List of Threatened Species. IUCN, Gland, Switzerland and Cambridge, UK

  • Holtsford TP (1996) Variation in inbreeding depression among families and populations of Clarkia tembloriensis (Onagraceae). Heredity 76:83–91

    Google Scholar 

  • Husband BC, Barrett SCH (1992) Genetic drift and the maintenance of the style length polymorphism in trystylous populations of Eichornia paniculata (Pontederiaceae). Heredity 69:440–449

    Google Scholar 

  • Husband BC, Schemske DW (1996) Evolution of the magnitude and timing of inbreeding depression in plants. Evolution 50:50–74

    Article  Google Scholar 

  • Husband BC, Schemske DW (1997) The effect of inbreeding in diploid and tetraploid populations of Epilobium angustifolium (Onagraceae): implications for the genetic basis of inbreeding depression. Evolution 51:737–746

    Article  Google Scholar 

  • Johnston MO, Schoen DJ (1996) Correlated evolution of self-fertilization and inbreeding depression: an experimental study of nine populations of Amsinckia (Boraginaceae). Evolution 50:1478–1491

    Article  Google Scholar 

  • Kalinowski ST, Hedrick PW (1999) Detecting inbreeding depression is difficult in captive endagered species. Anim Conserv 2:131–136

    Article  Google Scholar 

  • Keller LK, Waller DM (2003) Inbreeding effects in wild populations. Trends Ecol Evol 17:230–241

    Article  Google Scholar 

  • Lande R, Schemske DW (1985) The evolution of self-fertilization and inbreeding depression in plants. I. Genetic models. Evolution 39:29–40

    Article  Google Scholar 

  • Littell RC, Miliken GA, Stroup WW, Wolfinger RD (1996) SAS system for mixed models. SAS Institute Inc., Cary, North Carolina, USA

    Google Scholar 

  • Luijten S, Oostermeijer G, van Leeuwen N, den Nijs H (1996) Reproductive success and clonal genetic structure of the rare Arnica montana (Compositae) in The Netherlands. Plant Syst Evol 201:15–39

    Article  CAS  Google Scholar 

  • Masterson J (1994) Stomatal size in fossil plants: evidence for polyploidy in majority of Angiosperms. Science 264:421–424

    Article  PubMed  Google Scholar 

  • Mauchamp A (1997) Threats from alien plant species in the Galápagos Islands. Conserv Biol 11:260–263

    Article  Google Scholar 

  • Mauchamp A, Aldaz I, Edwin O, Valdebenito H (1998) Threatened species, a re-evaluation of the status of eight endemic plants of the Galápagos. Biodiversity Conserv 7:97–107

    Article  Google Scholar 

  • Nielsen LR (2004) Molecular differentiation within and among island populations of the endemic plant Scalesia affinis (Asteraceae) from the Galápagos Islands. Heredity 93:434–442

    Article  PubMed  CAS  Google Scholar 

  • Nielsen LR, Philipp M, Adsersen H, Siegismund HR (2000). Breeding system of Scalesia divisa Andersson, an endemic Asteraceae from the Galápagos Islands. Det Norske Videnskaps-Akademi. I. Mat-Naturv Klasse, Skrifter, Ny Serie 39:127–138

    Google Scholar 

  • Nielsen LR, Siegismund HR, Philipp M (2003) Partial self-incompatibility in the polyploid endemic species Scalesia affinis (Asteraceae) from the Galápagos: remnants of a self-incompatibility system? Bot J Linn Soc 142:93–101

    Article  Google Scholar 

  • Norman J, Sakai AK, Weller SG, Dawson TE (1995) Inbreeding depression in morphological and physiological traits of Schiedea lydgatei (Caryophyllaceae) in two environments. Evolution 49:297–306

    Article  Google Scholar 

  • Picó FX, Joop Ouborg N, Van Groenendael JM (2004) Evaluation of the extent of among-family variation in inbreeding depression in the perennial herb Scabiosa columbaria (Dipsacaceae). Am J Bot 91:1183–1189

    Google Scholar 

  • Reid WV, Miller KR (1989) Keeping options alive: the scientific basis for conserving biodiversity. World Resources Institute, Washington, DC

    Google Scholar 

  • Reinartz JA, Les DH (1994) Bottleneck-induced dissolution of self-incompatibility and breeding system consequences in Aster furcatus (Asteraceae). Am J Bot 81:446–455

    Article  Google Scholar 

  • Rosquist G (2001) Reproductive biology in diploid Anthericum ramosum and tetraploid A. liliago (Anthericaceae). Oikos 92:143–152

    Article  Google Scholar 

  • SAS Institute (1990) SAS user’s guide: statistics. SAS Institute, Cary, North Carolina, USA

    Google Scholar 

  • Schemske DW (1983) Breeding system and habitat effects on fitness components in three neotropical Costus (Zingiberaceae). Evolution 37:523–539

    Article  Google Scholar 

  • Schemske DW, Husband BC, Ruckelshaus MH, Goodwille C, Parker IM, Bishop JG (1994) Evaluating approaches to the conservation of rare and endangered plants. Ecology 74:584–606

    Article  Google Scholar 

  • Schoen DJ (1983) Relative fitness of selfed and outcrossed progeny in Gilia achilleifolia (Polemoniaceae). Evolution 37:292–301

    Article  Google Scholar 

  • Soltis PS, Soltis DE (2000) The role of genetic and genomic attributes in the success of polyploids. Proc Natl Acad Sci USA 97:7051–7057

    Article  PubMed  CAS  Google Scholar 

  • Stebbins GL (1947) Types of polyploids: their classification and significance. Adv Genet 1:403–429

    Article  Google Scholar 

  • Templeton AR, Read B (1983) The elimination of inbreeding depression in a captive herd of Speke’s gazelle. In: Schoenwald-Cox CM, Chambers M, MacBryde B, Thomas L (eds) Genetics and conservation: a reference for managing wild animal and plant populations. Benjamin/Cummings, London, UK, pp 241–261

    Google Scholar 

  • Therneau TM (1996) Extending the Cox Model. Technical Report # 58:1996. Technical Report Series, Section of Biostatistics, Mayo Clinic, Rochester, Minnesota. Available at URL: www.mayo.edu/hsr/techrpt/58.pdf

  • Waller DM (1993) The statistics and dynamics of mating system evolution. In: Thornhill N (ed) The Natural history of inbreeding and outbreeding. University of Chicago Press, Chicago pp 97–117

    Google Scholar 

  • Young A, Miller C, Gregory E, Langston A (2000) Sporophytic self-incompatibility in diploid and tetraploid races of Rutidosis leptorrhynchoides (Asteraceae). Aust J Bot 48:667–672

    Article  Google Scholar 

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Acknowledgements

Ole Hamann, the Botanic Garden of the University of Copenhagen, is warmly acknowledged for allowing greenhouse space to our plants and Jimmy Olsen for taking care of the seedlings of Scalesia affinis. Thure Hauser, Eline Deirdre Lorenzen and Gitte Petersen are thanked for critical comments on previous versions of the manuscript. We thank The Danish Natural Science Research Council (grant no. 9601412) and the Carlsberg Foundation (ANS 1276/20) for financial support.

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Correspondence to Lene R. Nielsen.

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Nielsen, L.R., Siegismund, H.R. & Hansen, T. Inbreeding depression in the partially self-incompatible endemic plant species Scalesia affinis (Asteraceae) from Galápagos islands. Evol Ecol 21, 1–12 (2007). https://doi.org/10.1007/s10682-006-9128-6

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