Skip to main content
Log in

Relationship between population size, allozyme variation, and plant performance in the narrow endemic Cochlearia bavarica

  • Published:
Conservation Genetics Aims and scope Submit manuscript

Abstract

We studied population viability in relation topopulation size and allelic variation in thenarrowly-endemic, monocarpic perennial plantCochlearia bavarica in Bavaria. In 1996,we analysed allelic variation by allozymeelectrophoresis in 24 populations ranging from8–2000 flowering individuals. Fitness-relatedcharacters were investigated in 22 of the 24populations in the field in 1996 (reproductiveand vegetative traits) and 1998 (reproductivetraits only). Differences in allozyme patternwere large between a south-eastern and awestern population group. Genetic diversity,assessed by the Shannon-Wiener diversity index,was low within but high among populations.Small populations had fewer alleles per locus,fewer polymorphic loci, lower observedheterozygosity, and lower genetic diversitythan large populations. Environmentalvariables were not significantly correlatedwith population size or fitness with theexception of light availability, indicatingthat habitat quality was similar for large andsmall populations. Population size showedpositive correlations with number of flowers,fruit set per plant, number of seeds per fruit,and total seed output per plant. Fruit set andnumber of seeds per fruit were positivelycorrelated with the observed heterozygosity andthe proportion of polymorphic loci. We usedpath analyses to study the possible causalrelationships among population size, allelicvariation, and reproductive characters. Thesemodels showed that allelic variation had nodirect influence on reproductive characters,whereas population size did. We conclude thatat present population size reduces viabilityand also reduces allelic variation; but thereduced allelic variation may in the longerterm have negative feed-backs on bothpopulation size and viability.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Abs C (1999) Differences in the life history of two Cochlearia-species. In: Ecology of closely related plant species (eds. Marhold K, Schmid B, Krahulec F), pp. 33–45. Opulus Press, Uppsala.

    Google Scholar 

  • Ågren J (1996) Population size, pollinator limitation and seed set in the self-incompatible herb Lythrum salicaria. Ecology, 77, 1779–1790.

    Google Scholar 

  • Aizen MA, Feinsinger P (1994) Forest fragmentation, pollination and plant reproduction in a Chaco dry forest, Argentina. Ecology, 75, 330–351.

    Google Scholar 

  • Barrett SCH, Kohn JR (1991) Genetic and evolutionary consequences of small population size in plants: Implications for conservation. In: Genetics and conservation of rare plants (eds. Falk DA, Holsinger KH), pp. 3–30. Oxford University Press, Oxford.

    Google Scholar 

  • Bentler PM (1995) EQS Structural Equations. Encino, California.

  • Buza L, Young A, Thrall, P (2000) Genetic erosion, inbreeding and reduced fitness in fragmented species of the endangered tetraploid pea Swainsona recta. Biol. Conserv., 93, 177–186.

    Google Scholar 

  • Campbell DR, Halama JH (1993) Resource and pollen limitation to lifetime seed production in a natural plant population. Ecology, 74, 1043–1051.

    Google Scholar 

  • Dolan RW (1994) Patterns of allozyme variation in relation to population size, isolation and phytogeographic history in royal catchfly Silene regia: Caryophyllaceae). Am. J. Bot., 81, 965–972.

    Google Scholar 

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

    Google Scholar 

  • Falconer DS (1989) Introduction to Quantitative Genetics, 2nd edn. Longman, London.

    Google Scholar 

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

    Google Scholar 

  • Fischer M, Stöcklin J (1997) Local extinction of plants in remnants of extensively used calcareous grassland 1950–1985. Conserv. Biol., 11, 727–737.

    Google Scholar 

  • Fischer M, Matthies D (1998a) Effects of population size on performance in the rare plant Gentianella germanica. J. Ecol., 86, 195–204.

    Google Scholar 

  • Fischer M, Matthies D (1998b) RAPD variation in relation to population size and plant performance in the rare Gentianella germanica. Am. J. Bot., 85, 811–819.

    Google Scholar 

  • Fischer M, Husi R, Prati D, Peintinger M, van Kleunen M, Schmid B (2000) RAPD variation among and within small and large populations of the rare clonal plant Ranunculus reptans (Ranunculaceae). Am. J. Bot., 87, 1128–1137.

    Google Scholar 

  • Fischer M, Hock M, Paschke M (submitted) Low genetic variation reduces cross-compatibility and offspring fitness in populations of a narrow endemic self-incompatible plant.

  • Fritz AL, Nilsson A (1994) How pollinator-mediated mating varies with population size in plants. Oecologia, 100, 451–462.

    Google Scholar 

  • Gillet EM (1994) Genetic Structures from Electrophoresis Data (GSE). Version 1.1.b. Göttingen.

  • Gilpin ME, Soulé ME (1986) Minimum viable populations: Processes of extinction. In: Conservation Biology: The Science of Scarcity and Diversity (ed. Soulé ME), pp. 19–34. Sinauer, Sunderland.

    Google Scholar 

  • Gorchov DL (1988) Effects of pollen and resources on seed set and other fitness components in Amelanchier aborea (Rosaceae: Maloideae). Am. J. Bot., 75, 1275–1285.

    Google Scholar 

  • Groom MJ (1998) Allee effects limit population viability of an annual plant. Am. Nat., 151, 487–495.

    Google Scholar 

  • Hamrick JL, G odt MJW(1989) Allozyme diversity in plant species. In: Plant Population Genetics, Breeding and Genetic Resources (eds. Brown AHD, Clegg MT, Kahler AL, Weir BS), pp. 43–46. Sinauer, Sunderland.

    Google Scholar 

  • Jennersten O (1988) Pollination in Dianthus deltoides (Carophyllaceae): Effects of habitat fragmentation on visitation and seed set. Conserv. Biol., 4, 359–366.

    Google Scholar 

  • Jennersten O, Nilsson SG (1993) Insect flower visitation frequency and seed production in relation to patch size of Viscaria vulgaris (Carophyllaceae). Oikos, 68, 283–292.

    Google Scholar 

  • Karron JD (1987) A comparison of levels of genetic polymorphism and self-compatibility in geographically restricted and widespread plant congeners. Evol. Ecol., 1, 47–58.

    Google Scholar 

  • Kéry 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.

    Google Scholar 

  • Koch M, Hurka H, Huthmann M (1998) Isozymes, speciation and evolution in the polyploid complex Cochlearia L. (Brassicaceae). Bot. Acta, 111, 411–425.

    Google Scholar 

  • Kunin WE (1997) Population size and density effects in pollination: Pollinator foraging and plant reproductive success in experimental arrays of Brassica kaber. J. Ecol., 85, 225–234.

    Google Scholar 

  • Lacy RC (1987) Loss of genetic diversity from managed populations: Interacting effects of drift, mutation, immigration, selection and population subdivision. Conserv. Biol., 1, 143–158.

    Google Scholar 

  • Lammi A, Siikamaki P, Mustajarvi K. (1999) Genetic diversity, population size, and fitness in central and peripheral populations of a rare plant Lychnis viscaria. Conserv. Biol., 13, 1069–1078.

    Google Scholar 

  • Leberg PL (1996) Applications of Allozyme Electrophoresis in Conservation Biology. In: Molecular Genetic Approaches in Conservation (eds. Smith TB, Wayne RK), pp. 87–103. Oxford University Press, Oxford.

    Google Scholar 

  • Lynch M, Conery J, Bürger R (1995) Mutational meltdowns in sexual populations. Evolution, 49, 1067–1080.

    Google Scholar 

  • Manly BFJ (1991) Randomization and Monte Carlo Methods in Biology. Chapman and Hall, London.

    Google Scholar 

  • Menges ES (1990) Population viability analysis for an endangered plant. Conserv. Biol., 4, 52–62.

    Google Scholar 

  • Menges ES (1991a) The application of minimum viable population theory to plants. In: Genetic and Conservation of Rare Plants (eds. Falk DA, Holsinger KH), pp. 45–61. Oxford University Press. Oxford.

    Google Scholar 

  • Menges ES (1991b) Seed germination percentage increases with population size in a fragmented prairie species. Conserv. Biol., 5, 158–164.

    Google Scholar 

  • Morgan JW (1999) Effects of population size on seed production and germinability in an endangered, fragmented grassland plant. Conserv. Biol., 13, 266–273.

    Google Scholar 

  • Müller-Starck G (1997) Allozymes. In: Molecular Tools for screening Diversity: Plants and Animals (eds. Karp A, Isaac PG, Ingram DS), pp. 75–81. Chapman and Hall, London.

    Google Scholar 

  • Olesen JM, Jain SK (1994) Fragmented plant populations and their lost interactions. In: Conservation Genetics (eds. Loeschke V, Tomiuk J, Jain SK), pp. 417–426. Birkhäuser, Basel.

    Google Scholar 

  • O'Neil P (1994) Genetic incompatibility and offspring quality in the tristylous plant Lythrum salicaria (Lythraceae). Am. J. Bot., 81, 76–84.

    Google Scholar 

  • Oostermeijer JGB, den Nijs JCM, Raijman LEL, Menken SBJ (1992) Population biology and management of the marsh gentian Gentiana pneumonanthe L., a rare species in The Netherlands. Bot. J. Linn. Soc., 108, 117–129.

    Google Scholar 

  • Oostermeijer JGB, Van Eijck MW, Den Nijs JCM (1994) Offspring fitness in relation to population size and allelic variation in the rare perennial plant species Gentiana pneumonanthe (Gentianaceae). Oecologia, 97, 289–296.

    Google Scholar 

  • Oostermeijer JGB, Van Eijck MW, Van Leeuwen NC, Den Nijs JCM (1995) Analysis of the relationship between allozyme heterozygosity and fitness in the rare Gentiana pneumonanthe L. J. Evol. Biol., 8, 739–759.

    Google Scholar 

  • Oostermeijer JGB, Berholz A, Poschlod P (1996) Genetic aspects of fragmented plant populations. In: Species Survival in Fragmented Landscapes (eds. Settele CR, Poschlod P, Henle K), pp. 93–101. Kluwer Academic Publishers, Amsterdam.

    Google Scholar 

  • Ouborg NJ, Van Treuren R (1994) The significance of genetic erosion in the process of extinction IV: Inbreeding load and heterosis in relation to population size in the mint Salvia pratensis. Evolution, 48, 996–1008.

    Google Scholar 

  • Payne RW (1993) Genstat 5, Version 3. Reference Manual. Clarendon Press, Oxford.

    Google Scholar 

  • Pitelka LF, Stanton DS, Peckenham MO (1980) Effects of light and density on resource allocation in a forest herb, Aster acuminatus (Compositae). Am. J. Bot., 67, 942–948.

    Google Scholar 

  • Raijmann LLE, Van Leeuwen NC, Kersten R, Oostermeijer JGB, Den Nijs HCM, Menken SBJ (1994) Allelic variation and outcrossing rate in relation to population size in Gentiana pneumonanthe. Conserv. Biol., 8, 1014–1026.

    Google Scholar 

  • Rajora OP, Mosseler A, Major JE (2000) Indicators of population viability in red spruce, Picea rubens. II. Genetic diversity, population structure, and mating behavior. Can. J. Bot., 78, 941–956.

    Google Scholar 

  • Roger DL (1997) Inheritance of allozymes from seed tissues of the hexaploid gymnosperm Sequoia sempervirens (Coast redwood). Heredity, 78, 166–175.

    Google Scholar 

  • Savolainen O, Henrick P (1995) Heterozygotes and fitness: No association in scots pine. Genetics, 140, 755–766.

    Google Scholar 

  • Schmidt K, Jensen K (2000). Genetic structure and AFLP variation of remnant populations in the rare plant Pedicularis palustris (Scrophulariaceae) and its relation to population size and reproductive components. Am. J. Bot., 87, 678–689.

    Google Scholar 

  • Shannon CE, Wiener W (1949) The Mathematical Theory of Communication. University of Illinois Press, Urbana.

    Google Scholar 

  • Shaffer ML (1981) Minimal population sizes for species conservation. BioScience, 31, 131–134.

    Google Scholar 

  • Sobrevila C (1988) Effects of distance between pollen donor and pollen recipient on fitness components in Espeletia schultzii. Am. J. Bot., 75, 701–724.

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. Freeman, San Francisco, California.

    Google Scholar 

  • Stebbins GL (1980) Polyploidy in plants: Unsolved problems and prospects. In: Polyploidy: Biological Relevance (ed. Lewis WH), pp. 495–520. New York.

  • Sun M (1996) Effects of population size, mating system, and evolutionary origin on genetic diversity in Spiranthes sinensis and S. hongkongensis. Conserv. Biol., 10, 785–795.

    Google Scholar 

  • Van Treuren R, Bijlsma R, Ouborg NJ, Van Delden W (1991) The significance of genetic erosion in the process of extinction: I. Genetic differentiation in Salvia pratensis L. and Scabiosa columbaria L. in relation to population size. Heredity, 66, 181–189.

    Google Scholar 

  • Van Treuren R, Bijlsma R, Ouborg NJ, Van Delden W (1993) The significance of genetic erosion in the process of extinction. IV. Inbreeding depression and heterosis effects caused by selfing and outcrossing in Scabiosa columbaria. Evolution, 47, 1669–1680.

    Google Scholar 

  • Vogt R (1985) Die Cochlearia pyrenaica-Gruppe in Zentraleuropa. Ber. Bayer. Bot. Ges., 59, 133–135.

    Google Scholar 

  • Washitani I, Osawa R, Namai H, Niwa M (1994) Patterns of female fertility in heterostylous Primula sieboldii under severe pollinator limitation. J. Ecol., 82, 571–579.

    Google Scholar 

  • Williamson PS, Werth CR (1999) Levels and patterns of allelic variation in the endangerd species Abronia macrocarpa (Nyctaginaceae). Am. J. Bot., 86, 293–301.

    Google Scholar 

  • Wolfe LM (1995) The genetics and ecology of seed size variation in a biennial plant, Hydrophyllum appendiculatum (Hydrophyllaceae). Oecologia, 101, 343–352.

    Google Scholar 

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

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Melanie Paschke.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Paschke, M., Abs, C. & Schmid, B. Relationship between population size, allozyme variation, and plant performance in the narrow endemic Cochlearia bavarica . Conservation Genetics 3, 131–144 (2002). https://doi.org/10.1023/A:1015293530776

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1015293530776

Navigation