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Effects of population size on genetic diversity, fitness and pollinator community composition in fragmented populations of Anthericum liliago L.

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Abstract

The genetic and fitness consequences of habitat fragmentation on the dry grassland species Anthericum liliago L. (Anthericaceae) were examined. We used random amplified polymorphic DNA (RAPD) markers to determine the distribution of genetic diversity within and among 10 German A. liliago populations, ranging in size from 116 to over 2 million ramets. The genetic diversity of an A. liliago population was highly positively correlated with its population size. The overall differentiation among populations (Phi-ST = 0.41, P < 0.0001, AMOVA) was considerably higher than expected for a species with a mixed breeding system. No strong correlation (P < 0.01) was detected between fitness parameters and population size and genetic diversity. The reproductive output (seeds per ramet) was only highly correlated (P < 0.001) with the proportion of flowering ramets in a population which could be caused by a more effective pollination in large populations which are more attractive to specialized pollinators. The specialized A. liliago pollinator Merodon rufus (Syrphidae) and high abundances of solitary bees could only be found in A. liliago populations with more than 10,000 individuals. Genetic differentiation among the investigated A. liliago populations may have been caused by limited seed and pollen dispersal and a mixed mating system permitting a high selfing rate. The differentiation among the small and isolated populations lacking main pollinators seems to be caused by genetic drift.

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References

  • Allen-Wardell G, Bernhardt P, Bitner R et al (1998) The potential consequences of pollinator declines on the conservation of biodiversity and stability of food crop yields. Conserv Biol 12:8–17

    Article  Google Scholar 

  • Brys R, Jacquemyn H, Endels P et al (2004) Reduced reproductive success in small populations of the self-incompatible Primula vulgaris. J Ecol 92:5–14

    Article  Google Scholar 

  • Bussel JD (1999) The distribution of random amplified polymorphic DNA (RAPD) diversity amongst populations of Isotoma petraea (Lobeliaceae). Mol Ecol 8:775–789

    Article  Google Scholar 

  • Campbell LG, Husband BC (2007) Small populations are mate-poor but pollinator-rich in a rare, self-incompatible plant, Hymenxys herbaceae (asteraceae). New Phytol 174:915–925

    Article  PubMed  CAS  Google Scholar 

  • Culley TM, Grubb TC (2003) Genetic effects of habitat fragmentation in Viola pubescens (Violaceae), a perennial herb with chasmogamous and cleistogamous flowers. Mol Ecol 12:2919–2930

    Article  PubMed  Google Scholar 

  • Excoffier L, Smouse PE, Quattro JM (1992) Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131:479–491

    PubMed  CAS  Google Scholar 

  • Fischer M, Matthies D (1998) RAPD variation in relation to population size and plant fitness in the rare Gentianella germanica (Gentianaceae). Am J Bot 8:811–819

    Article  Google Scholar 

  • Frankham R (1996) Relationship of genetic variation to population size in wildlife. Conserv Biol 10:1500–1508

    Article  Google Scholar 

  • Gathmann A, Tscharnke T (2002) Foraging ranges of solitary bees. J Animal Ecol 71:757–764

    Article  Google Scholar 

  • Hensen I, Oberprieler C (2005) Effects of population size on genetic diversity and seed production in the rare Dictamnus albus (Rutaceae) in central Germany. Conserv Genet 6:63–73

    Article  Google Scholar 

  • Hensen I, Oberprieler C, Wesche K (2005) Genetic structure, population size, and seed production of Pulsatilla vulgaris Mill. (Ranunculaceae) in Central Germany. Flora 200:3–14

    Google Scholar 

  • Huff DR, Peakall R, Smouse PE (1993) RAPD variation within and among natural populations of outcrossing buffalograss (Buchloe dactyloides (Nutt.) Engelm.). Theor Appl Genet 86:927–934

    Article  CAS  Google Scholar 

  • Jackel AK (1999) Strategien der Pflanzenarten einer fragmentierten Trockenrasengesellschaft. J. Cramer, Berlin, Stuttgart

    Google Scholar 

  • Jacquemyn H, Van Rossum F, Brys R et al (2003) Effects of agricultural land use and fragmentation on genetics, demography and population persistence of the rare Primula vulgaris, and implications for conservation. Belg J Bot 136:5–22

    Google Scholar 

  • Jentzsch M, Köberlein T (2000) Zur Schwebfliegen-Fauna des Naturschutzgebietes "Hasenwinkel” im Landkreis Mansfelder Land mit Bemerkungen zur Biologie von Merodon rufus MEIGEN 1838 und Eumerus strigatus (FALLEN, 1817) (Dipt., Syrphidae). Entomolog Nachr Ber 44:189–192

    Google Scholar 

  • Kery M, Matthies D, Spillmann HH (2000) Reduced fecundity and offspring performance in small populations of the declining grassland plants Primula veris and Gentiana lutea. J Ecol 88:17–30

    Article  Google Scholar 

  • Kirvan AP (1997) Latitude/Longitude, NCGIA Core Curriculum in GI Science. http://www.ncgia.ucsb.edu/giscc/units/u014/u014html. Accessed 29 Nov 2005

  • Kolseth AK, Lonn M, Svensson BM (2005) Genetic structure in two meadow varieties of Euphrasia stricta on the Baltic Island of Gotland (Sweden) and implications for conservation. Folia Geobot 40:163–176

    Article  Google Scholar 

  • Kwak MM, Velterop O, van Andel J (1998) Pollen and gene flow in fragmented habitats. Appl Veg Sci 1:37–54

    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 

  • Llorens TM, Ayre DJ, Whelan RJ (2004) Evidence for ancient genetic subdivision among recently fragmented populations of the endangered shrub Grevillea caleyi (Proteaceae). Heredity 92:519–526

    Article  PubMed  CAS  Google Scholar 

  • Luijten SH, Dierick A, Gerard J et al (2000) Population size, genetic variation, and reproductive success in a rapidly declining, self-incompatible perennial (Arnica montana) in the Netherlands. Conserv Biol 14:1776–1787

    Article  Google Scholar 

  • Lynch M, Milligan BG (1994) Analysis of population genetic structure with RAPD markers. Mol Ecol 3:91–99

    Article  PubMed  CAS  Google Scholar 

  • Matthies D, Brauer I, Maibom W et al (2004) Population size and the risk of local extinction: empirical evidence from rare plants. Oikos 105:481–488

    Article  Google Scholar 

  • Mavraganis K, Eckert CG (2001) Effects of population size and isolation on reproductive output in Aquilegia canadensis (Ranunculaceae). Oikos 95:300–310

    Article  Google Scholar 

  • Monaghan BG, Halloran GM (1996) RAPD variation within and between natural populations of morama [Tylosema esculentum (Burchell) Schreiber] in Southern Africa. South African J Bot 62:287–291

    Google Scholar 

  • Müller-Schärer H, Fischer M (2001) Genetic structure of the annual weed Senecio vulgaris in relation to habitat type and population size. Mol Ecol 10:17–28

    Article  PubMed  Google Scholar 

  • Nybom H, Bartish IV (2000) Effects of life history traits and sampling strategies on genetic diversity estimates obtained with RAPD markers in plants. Perspectives Plant Ecol Evol Syst 3:93–114

    Article  Google Scholar 

  • Paschke M, Abs C, Schmid B (2002) Relationship between population size, allozyme variation, and plant performance in the narrow endemic Cochlearia bavarica. Conserv Genet 3:131–144

    Article  CAS  Google Scholar 

  • Peterson A, Bartish IV, Peterson J (2002) Genetic structure detected in a small population of the endangered plant Anthericum liliago (Anthericaceae) by RAPD analysis. Ecography 25:677–684

    Article  Google Scholar 

  • Reisch C, Poschlod P, Wingender R (2003) Genetic differentiation among populations of Sesleria albicans Kit. ex Schultes (Poaceae) from ecologically different habitats in central Europe. Heredity 91:519–527

    Article  PubMed  CAS  Google Scholar 

  • Rennwald E (ed) (2000) Verzeichnis und Rote Liste der Pflanzengesellschaften Deutschlands. Schriftenreihe für Vegetationskunde 35. Bonn-Bad Godesberg

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

    Article  Google Scholar 

  • Rosquist G, Prentice HC (2002) Genetic variation in Scandinavian Anthericum liliago (Anthericaceae): allopolyploidy, hybridization and immigration history. Plant Syst Evol 236:55–72

    Article  CAS  Google Scholar 

  • Schneider S, Roessli D, Excoffier L (2000) ARLEQUIN: a software for population genetics data analysis.Version 2.000. University of Geneva, Geneva, Switzerland

  • Steffan-Dewenter I, Tscharntke T (1999) Effects of habitat isolation on pollinator communities and seed set. Oecologia 12:432–440

    Article  Google Scholar 

  • Williams JGK, Kubelik AR, Livak KJ et al (1990) DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucl Acids Res 18:6531–6535

    Article  PubMed  CAS  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  Google Scholar 

Download references

Acknowledgements

We are grateful to Martin Trost for creation of Fig. 1, Matthias Jentzsch and Eckart Stolle for the determination of M. rufus and Tobias Meitzel for the determination of solitary bees.

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Authors and Affiliations

  1. Biozentrum, Martin-Luther-University of Halle-Wittenberg, Weinbergweg 22, 06120, Halle/Saale, Germany

    Angela Peterson

  2. Université de Rennes 1 Unité Mixte de Recherche CNRS 6553 « Ecobio »: Ecosystèmes – Biodiversité – Evolution, Campus de Beaulieu, Bâtiment 14A, 263 Avenue du Général Leclerc, 35042, Rennes Cedex, France

    Igor V. Bartish

  3. State Office for Environmental Protection of Saxony-Anhalt, Reideburger Str. 47, 06116, Halle/Saale, Germany

    Jens Peterson

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  1. Angela Peterson
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  2. Igor V. Bartish
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  3. Jens Peterson
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Correspondence to Angela Peterson.

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Peterson, A., Bartish, I.V. & Peterson, J. Effects of population size on genetic diversity, fitness and pollinator community composition in fragmented populations of Anthericum liliago L.. Plant Ecol 198, 101–110 (2008). https://doi.org/10.1007/s11258-007-9388-4

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  • DOI: https://doi.org/10.1007/s11258-007-9388-4

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