Skip to main content

Advertisement

Log in

No Correlation Between Heterozygosity and Vegetative Fitness in the Narrow Endemic and Critically Endangered Clematis acerifolia (Ranunculaceae)

  • Published:
Biochemical Genetics Aims and scope Submit manuscript

Abstract

The relationship between heretozygosity and vegetative fitness was explored in the narrow endemic and threatened Clematis acerifolia (Ranunculaceae), both at individual and population levels. The relationships between fitness, habitat factors, and population size were also analyzed. Allozyme electrophoresis was used to quantify the levels of heterozygosity of nearly 200 surveyed individuals belonging to the nine extant populations of this species. Six parameters of vegetative fitness were measured: plant height, shrub diameter, length of the largest leaf, width of the largest leaf, mean number of leaves/stem, and total number of stems. The percentage of tree cover (light availability) was measured as an indicator of habitat quality. A principal component analysis reduced the original fitness variables to two uncorrelated principal components. None of these correlated significantly with both heterozygosity and population size, in contrast to the expected result. Nevertheless, one of the principal components showed a positive relationship with light availability, which may indicate that habitat quality may have significant effects on the performance of this species. Thus, to ensure the viability of this endangered species, maintenance of adequate habitat quality (by avoiding further fragmentation) may be more important than maximizing genetic diversity within populations.

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.

Fig. 1

Similar content being viewed by others

References

  • Allendorf FW, Leary RF (1986) Heterozygosity and fitness in natural populations of animals. In: Soulé M (ed) Conservation biology: the science of scarcity and diversity. Sinauer, Sunderland, pp 57–76

    Google Scholar 

  • Boerrigter EJM (1995) On the perspectives of populations of the rare plant species Phyteuma nigra. Ph.D. Thesis, State University of Groningen, The Netherlands

  • Booy G, Hendriks RJJ, Smulders MJM, van Groenendael JM, Vosman B (2000) Genetic diversity and the survival of populations. Plant Biol 2:379–395

    Article  Google Scholar 

  • Bosch M, Waser NM (1999) Effects of local density on pollination and reproduction in Delphinium nuttallianum and Aconitum columbianum (Ranunculaceae). Am J Bot 86:871–879

    Article  PubMed  Google Scholar 

  • Britten H B (1996) Meta-analyses of the association between multilocus heterozygosity and fitness. Evolution 50:2158–2164

    Article  Google Scholar 

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

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Clayton JW, Tretiak DN (1972) Amino-citrate buffers for pH control in starch gel electrophoresis. J Fish Res Board Can 29:1169–1172

    CAS  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 

  • Fennema F (1990) Effects of exposure to atmospheric SO2, NH3 and (NH4)2SO4 on survival and extinction of Arnica montana L. and Viola canina L, Report Research Institute for Nature Management 90/14, Arnhem, The Netherlands

  • Fischer M, Matthies D (1997) Mating structure and inbreeding and outbreeding depression in the rare plant Gentianella germanica (Gentianaceae). Am J Bot 84:1685–1692

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Frankham R (2005) Genetics and extinction. Biol Conserv 126:131–140

    Article  Google Scholar 

  • Gaston KJ, Blackburn TM, Greenwood JJD, Gregory RD, Quinn RM, Lawton JH (2000) Abundance-occupancy relationships. J Appl Ecol 37:39–59

    Article  Google Scholar 

  • Gong WZ, Long YY, Li MX (1985) Karyotype studies on Clematis from Beijing, China. J Wuhan Bot Res 3:371–379

    Google Scholar 

  • Hansson B, Westerberg L (2002) On the correlation between heterozygosity and fitness in natural populations. Mol Ecol 11:2467–2474

    Article  PubMed  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 

  • IUCN (2001) IUCN Red List Categories and Criteria: Version 3.1, UCN Species Survival Commission, Gland and Cambridge

  • Kéry M, Matthies D, Spillmann H-H (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 

  • Kimura M (1983) The neutral theory of molecular evolution. Cambridge University Press, Cambridge

    Google Scholar 

  • Knowles P, Mitton JB (1980) Genetic heterozygosity and radial growth variability in Pinus contorta. Silvae Genet 29:114–118

    Google Scholar 

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

    Article  Google Scholar 

  • Lienert J, Fischer M, Schneller J, Diemer M (2002) Isozyme variability of the wetland specialist Swertia perennis (Gentianaceae) in relation to habitat size, isolation, and plant fitness. Am J Bot 89:801–811

    Article  CAS  Google Scholar 

  • Linhart Y, Mitton JB (1985) Relationships among reproduction, growth rates, and protein heterozygosity in ponderosa pine. Am J Bot 72:181–184

    Article  Google Scholar 

  • López-Pujol J, Zhang F-M, Ge S (2005) Population genetics and conservation of the critically endangered Clematis acerifolia (Ranunculaceae). Can J Bot 83:1248–1256

    Article  CAS  Google Scholar 

  • Luijten SH, Dierick A, Oostermeijer JGB, Raijmann LEL, den Nijs HCM (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 

  • Mitton JB (1989) Physiological and demographic variation associated with allozyme variation. In: Soltis DE, Soltis PS (eds) Isozymes in plant biology. Dioscorides Press, Portland, pp 127–145

    Google Scholar 

  • Mitton JB (1994) Molecular approaches to population biology. Annu Rev Ecol Syst 25:45–69

    Article  Google Scholar 

  • Mitton JB, Grant MC (1984) Associations among protein heterozygosity, growth rate, and developmental homeostasis. Annu Rev Ecol Syst 15:479–499

    Article  Google Scholar 

  • Nei M (1987) Molecular evolutionary genetics. Columbia University Press, New York

    Google Scholar 

  • Noel F, Machon N, Porcher E (2007) No genetic diversity at molecular markers and strong phenotypic plasticity in populations of Ranunculus nodiflorus, an endangered plant species in France. Ann Bot 99:1203–1212

    Article  PubMed  Google Scholar 

  • Ohta R (1971) Associative overdominance caused by linked detrimental mutations. Genet Res 18:277–286

    Article  Google Scholar 

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

    Google Scholar 

  • Oostermeijer JGB, Luijten SH, Krenová ZV, den Nijs JCM (1998) Relationships between population and habitat characteristics and reproduction of the rare Gentiana pneumonanthe L. Conserv Biol 12:1042–1053

    Article  Google Scholar 

  • Oostermeijer JGB, Luijten SH, den Nijs JCM (2003) Integrating demographic and genetic approaches in plant conservation. Biol Conserv 113:389–398

    Article  Google Scholar 

  • Orellana MR, López-Pujol J, Blanché C, Bosch M (2007) Relationships between heterozygosity and fitness in the Iberian threatened larkspur Delphinium bolosii (Ranunculaceae). Flora 202:161–168

    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 

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

    Article  Google Scholar 

  • Savolainen O, Hedrick P (1995) Heterozygosity and fitness: no association in scots pine. Genetics 140:755–766

    PubMed  CAS  Google Scholar 

  • Soltis DE, Haufler H, Darrow D, Gastony J (1983) Starch gel electrophoresis of ferns: a compilation of grinding buffers, gel and electrode buffers and staining schedules. Am Fern J 73:9–27

    Article  Google Scholar 

  • Spielman D, Brook BW, Frankham R (2004) Most species are not driven to extinction before genetic factors impact them. Proc Natl Acad Sci USA 101:15261–15264

    Article  PubMed  CAS  Google Scholar 

  • Thelen GC, Allendorf FW (2001) Heterozygosity-fitness correlations in rainbow trout: effects of allozyme loci or associative overdominance? Evolution 55:1180–1187

    PubMed  CAS  Google Scholar 

  • Vergeer P, Rengelink R, Copal A, Ouborg NJ (2003) The interacting effects of genetic variation, habitat quality and population size on performance of Succisa pratensis. J Ecol 91:18–26

    Article  CAS  Google Scholar 

  • Wang W-T (2002) A revision of Clematis sect. Cheiropsis (Ranunculaceae). Acta Phytotaxon Sin 40:193–241

    Google Scholar 

  • Wendel F, Weeden NF (1989) Visualization and interpretation of plant isozymes. In: Soltis DE, Soltis PS (eds) Isozymes in plant biology. Dioscorides Press, Portland, pp 5–45

    Google Scholar 

  • Yang Q-E (2002) Cytology of ten species in Anemone, one in Anemoclema and six in Clematis (Trib. Anemoneae, Ranunculaceae) from China. Acta Phytotaxon Sin 40:396–405

    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 

  • Zouros E, Foltz DW (1987) The use of allelic isozyme variation for the study of heterosis. In: Rattazzi MC, Scandalios JG, Whitt GS (eds) Isozymes: current topics in biological and medical research, vol 13, Alan R. Liss Publisher, New York, pp 1–59

    Google Scholar 

Download references

Acknowledgments

The authors thank Jing-Hua Shi and Ding Wu for their assistance in the field work, A-Man Zhao and Guo-Qin Yu for their help in experimental work, and Prof. Wen-Tsai Wang for his valuable comments. We also thank the Chinese Academy of Sciences (KSCX2-SW-106, KSCXZ-SW-101A) for financial support. This work was also subsidized by two grants from the Spanish Ministry of Education and Science to the first author, one for a predoctoral stay of two months at the Beijing Institute of Botany (2003) and the other (EX2005-0922) for two years of postdoctoral research (2006–2007) at the same institution.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jordi López-Pujol.

Rights and permissions

Reprints and permissions

About this article

Cite this article

López-Pujol, J., Zhang, FM. & Ge, S. No Correlation Between Heterozygosity and Vegetative Fitness in the Narrow Endemic and Critically Endangered Clematis acerifolia (Ranunculaceae). Biochem Genet 46, 433–445 (2008). https://doi.org/10.1007/s10528-008-9161-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10528-008-9161-y

Keywords

Navigation