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Asexual and sexual reproductive strategies in clonal plants

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Frontiers of Biology in China

Abstract

Most plants can reproduce both sexually and asexually (or vegetatively), and the balance between the two reproductive modes may vary widely between and within species. Extensive clonal growth may affect the evolution of life history traits in many ways. First, in some clonal species, sexual reproduction and sex ratio vary largely among populations. Variation in sexual reproduction may strongly affect plant’s adaptation to local environments and the evolution of the geographic range. Second, clonal growth can increase floral display, and thus pollinator attraction, while it may impose serious constraints and evolutionary challenges on plants through geitonogamy that may strongly influence pollen dispersal. Geitonogamous pollination can bring a cost to plant fitness through both female and male functions. Some co-evolutionary interactions, therefore, may exist between the spatial structure and the mating behavior of clonal plants. Finally, a trade-off may exist between sexual reproduction and clonal growth. Resource allocation to the two reproductive modes may depend on environmental conditions, competitive dominance, life span, and genetic factors. If different reproductive modes represent adaptive strategies for plants in different environments, we expect that most of the resources should be allocated to sexual reproduction in habitats with fluctuating environmental conditions and strong competition, while clonal growth should be dominant in stable habitats. Yet we know little about the consequence of natural selection on the two reproductive modes and factors which control the balance of the two reproductive modes. Future studies should investigate the reproductive strategies of clonal plants simultaneously from both sexual and asexual perspectives.

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References

  • Abrahamson W G (1975). Reproductive strategies in dewerries. Ecology, 56: 721–726

    Article  Google Scholar 

  • Aspinwall N, Christian T (1992). Clonal structure, genotypic diversity and seed production in populations of Filipendula rubra (Rosaceae) from the north central United States. American Journal of Botany, 79: 294–299

    Article  Google Scholar 

  • Back A J, Kron P, Stewart S C (1996). Phenological regulation of opportunities for within-inflorescence geitonogamy in the clonal species, Iris versicolor (Iridaceae). American Journal of Botany, 83: 1033–1040

    Article  Google Scholar 

  • Bai W N, Zhang D Y (2004). Dichogamy. In: Zhang D Y, ed. Life History Evolution and Reproductive Ecology in Plants. Beijing: Science Press, 284–301 (in chinese)

    Google Scholar 

  • Biere A (1995). Genotypic and plastic variation in plant size: effects on fecundity and allocation patterns in Lychnis flos-cuculi along a gradient of natural soil fertility. Journal of Ecology, 83: 629–642

    Article  Google Scholar 

  • Bostock S J (1980). Variation in reproductive allocation in Tussilago farfara. Oikos, 34: 359–363

    Article  Google Scholar 

  • Bowker M A, Stark L R, McLetchie D N, Mishler B D (2000). Sex expression, skewed sex ratios, and microhabitat distribution in the dioecious desert moss Syntrichia caninervis (Pottiaceae). American Journal of Botany, 87: 517–526

    Article  PubMed  Google Scholar 

  • Byers D L (1995). Pollen quantity and quality as explanations for low seed set in small populations exemplified by Eupatorium (Asteraceae). American Journal of Botany, 82: 1000–1006

    Article  Google Scholar 

  • Charpentier A (2002). Consequences of clonal growth for plant mating. Evolutionary Ecology, 15: 521–530

    Article  Google Scholar 

  • Charpentier A, Grillas P, Thompson J D (2000). The effects of population size limitation on fecundity in mosaic populations of the clonal macrophyte Scirpus Maritimus (Cyperaceae). American Journal of Botany, 87: 502–507

    Article  PubMed  Google Scholar 

  • Cook R E (1979). Asexual reproduction: A further consideration. American Naturalist, 113: 769–772

    Article  Google Scholar 

  • Cook R E (1985). Groth and development in clonal plant population. In: Jackson J B C, Buss L W, Cook R E, eds. Population Biology and Evolution of Clonal Organisms. New Haven: Yale University Press, 259–296

    Google Scholar 

  • de Kroon H, van Groenendael J (1997). The ecology and evolution of clonal plants. Leiden: Backhuys Publishers

    Google Scholar 

  • Dorken M E, Eckert C G (2001). Severely reduced sexual reproduction in northern populations of a clonal plant, Decodon verticillatus (Lythraceae). Journal of Ecology, 89: 339–350

    Article  Google Scholar 

  • Eckert C G (1999). Clonal plant research: proliferation,integration,but not much evolution. American Journal of Botany, 86: 1649–1654

    Article  Google Scholar 

  • Eckert C G (2000). Contributions of autogamy and geitonogamy to self-fertilization in a mass-flowering, clonal plant. Ecology, 81: 532–542

    Google Scholar 

  • Eckert C G (2002). The loss of sex in clonal plants. Evolutionary Ecology, 15: 501–520

    Article  Google Scholar 

  • Eckert C G, Barrett S C H (1992). Stochastic Loss of Style Morphs from Populations of Tristylous Lythrum-Salicaria and Decodon-Verticillatus (Lythraceae). Evolution, 46: 1014–1029

    Article  Google Scholar 

  • Eckert C G, Lui K, Bronson K, Corradini P, Bruneau A (2003). Population genetic consequences of extreme variation in sexual and clonal reproduction in an aquatic plant. Molecular Ecology, 12: 331–344

    Article  PubMed  Google Scholar 

  • Eriksson O (1997). Clonal life histories and the evolution of seed recruitment. In: de Kroon H, vanGroenendae J M, eds. The Ecology and Evolution of Clonal Plants. Leiden: Backhuys Publishers, 211–226

    Google Scholar 

  • Eriksson O, Jerling L (1990). Hierarchical selection and risk spreading in clonal plants. In: van-Groenendael J, de-Kroon H, eds. Clonal Growth in Plants: Regulation and Function. The Hague: SPB Academic Publishing, 79–84

    Google Scholar 

  • Gardner S N, Mangel M (1999). Modeling investments in seeds, clonal offspring, and translocation in a clonal plant. Ecology, 80: 1202–1220

    Google Scholar 

  • Hammerli A, Reusch T B H (2003a). Flexible mating: cross-pollination affects sex-expression in a marine clonal plant. Journal of Evolutionary Biology, 16: 1096–1105

    Article  PubMed  CAS  Google Scholar 

  • Hammerli A, Reusch T B H (2003b). Inbreeding depression influences genet size distribution in a marine angiosperm. Molecular Ecology, 12: 619–629

    Article  PubMed  CAS  Google Scholar 

  • Handel S N (1985). The intrusion of clonal growth patterns on plant breeding systems. American Naturalist, 125: 367–384

    Article  Google Scholar 

  • Harder L D, Barrett C H (1995). Mating cost of large floral displays in hermaphrodite plants. Nature, 373: 512–515

    Article  CAS  Google Scholar 

  • Hartemink N, Jongejans E, de Kroon H (2004). Flexible life history responses to flower and rosette bud removal in three perennial herbs. Oikos, 105: 159–167

    Article  Google Scholar 

  • Hartnett D C (1990). Size-dependent allocation to sexual and vegetative reproduction in four clonal composites. Oecologia, 84: 254–259

    Google Scholar 

  • Heywoods J S (1986). The effect of plant size variation on genetic drift in populations of annuals. American Naturalist, 127: 851–861

    Article  Google Scholar 

  • Holler L C, Abrahamson W G (1997). Seed and Vegetative Reproduction in Relation to Density in Fragaria-Virginiana (Rosaceae). American Journal of Botany, 64: 1003–1007

    Article  Google Scholar 

  • Klekowski E J J (1997). Somatic mutation theory of clonality. In: de Kroon H, van Groenenda J M, eds. The Ecology and Evolution of Clonal Plants. Leiden: Backuys Pubkisher, 227–241

    Google Scholar 

  • Liao W J (2004). Molecular markers. In: Zhang D Y, ed. Life History Evolution and Reproductive Ecology in Plants. Beijing: Science Press, 369–403 (in Chinese)

    Google Scholar 

  • Loehle C (1987). Partitioning of reproductive effort in clonal plants: a benefit-cost model. Oikos, 49: 199–208

    Article  Google Scholar 

  • Lopez F, Fungairino S, de la Heras P, Serrano J, Acosta F (2001). Age changes in the vegetative vs. reproductive allocation by module demographic strategies in a perennial plant. Plant Ecology, 157: 13–21

    Article  Google Scholar 

  • Lopez-Almansa J C, Pannell J R, Gil L (2003). Female sterility in Ulmus minor (Ulmaceae): a hypothesis invoking the cost of sex in a clonal plant. American Journal of Botany, 90: 603–609

    Google Scholar 

  • Lovett Doust, L L (1981). Population dynamics and local specialization in a clonal plant Tanunculus repens I. The dynamics of ramets in contrasting habitats. Journal of Ecology, 69: 743–755

    Article  Google Scholar 

  • Mclellan A J, Prati D, Kaltz O, Schmid B (1997). Structure and analysis of phenotypic and genetic variation in clonal plants. In: de Kroon H, van Groenenda J M, eds. The Ecology and Evolution of Clonal Plants. Leiden: Backhuys Publishers, 185–210

    Google Scholar 

  • McLetchie D N, Garcia-Ramos G, Crowley P H (2002). The local ratio dynamics: a model for the dioecious liverwort Marchantia inflexa. Evolutionary Ecology, 15: 231–254

    Article  Google Scholar 

  • Mendez M, Obeso J R (1993). Size-dependent reproductive and vegetative allocation in Arum italicum(Araceae). Candian Journal of Botany, 71: 309–314

    Article  Google Scholar 

  • Molau U, Prentice H C (1992). Repriductive system and population structure in three arctic Saxifraga spp. Jorunal of Ecology, 80: 149–161

    Article  Google Scholar 

  • Nishitami S, Takada T, Kachi N (1999). Optimal resource allocation to seeds and vegetative propagules under density-dependent regulation in Syneilesis palmata (Compositae). Plant Ecology, 141: 179–189

    Article  Google Scholar 

  • Oborny B, Bartha S (1995). Clonality in plant communities—an overview. Abstracta Botanica, 19: 115–127

    Google Scholar 

  • Pan J J, Price J S (2002). Fitness and evolution in clonal plants: the impact of clonal growth. Evolutionary Ecology, 15: 583–600

    Article  Google Scholar 

  • Philbrick C T, Les D H (1996). Evolution of aquatic angiosperm reproductive systems. Bioscience, 46: 813–826

    Article  Google Scholar 

  • Prati D, Schmid B (2000). Genetic differentiation of life-history traits within populations of the clonal plant Ranunculus reptans. Oikos, 90: 442–456

    Article  Google Scholar 

  • Rautiainen P, Koivula K, Hyvarinen M (2004). The effect of within-genet and between-genet competition on sexual reproduction and vegetative spread in Potentilla anserina ssp egedii. Journal of Ecology, 92: 505–511

    Article  Google Scholar 

  • Reekie E G (1991). Cost of seed versus rhizome production in Agropyron repens. Candian Journal of Botany, 69: 2678–2683

    Google Scholar 

  • Reekie E G (1999). Resource allocation, trade-offs, and reproductive effort in plants. In: Vuorisalo T O, Mutikainen P K, eds. Life History Evolution in Plants. Dordrecht: Kluwer Academic, 173–193

    Google Scholar 

  • Reusch T B H, Hukriede W, Stam W T, Olsen J L (1999). Differentiating between clonal growth and limited gene flow using spatial autocorrelation of microsatellites. Heredity, 2: 120–126

    Article  Google Scholar 

  • Reznick D (1985). Costs of reproduction: an evaluation of the empirical evidence. Oikos, 44: 257–267

    Article  Google Scholar 

  • Roff D A (1992). The evolution of life histories: theory and analysis. New York: Chapman and Hall

    Google Scholar 

  • Ronsheim M L, Bever J D (2000). Genetic variation and evolutionary trade-offs for sexual and asexual reproductive modes in Allium vineale(Liliaceae). American Journal of Botany, 87: 1769–1777

    Article  PubMed  Google Scholar 

  • Sakai S (1995). Optimal Resource-Allocation to Vegetative and Sexual Reproduction of a Plant-Growing in a Spatially Varying Environment. Journal of Theoretical Biology, 175: 271–282

    Article  Google Scholar 

  • Samson D A, Werk K S (1986). Size-dependent effects in the analysis of reproductive effort in plants. American Naturalist, 127: 667–680

    Article  Google Scholar 

  • Sato T (2002). Size-dependent resource allocation among vegetative propagules and male and female functions in the forest herb Laportea bulbifera. Oikos, 96: 453–462

    Article  Google Scholar 

  • Schmid B, Bazzaz F A (1995). Size dependency of sexual reproduction and of clonal growth in two perennial plants. Canadian Journal of Botany, 73: 1831–1837

    Article  Google Scholar 

  • Silander J A (1985). Microevolution in clonal plants. In: Jackson J B C, Buss L W, Cook R E, eds. Population Biology and Evolution of Clonal Organisms. London: Yale University Press, 107–152

    Google Scholar 

  • Stearns S C (1992). The evolution of life histories. Oxford: Oxford University Press

    Google Scholar 

  • Stebbins G L (1950). Variation and evolution in plants. New York: Columbia University Press

    Google Scholar 

  • Stuefer J F, Erschbamer B, Huber H, Suzuki J I (2002). The ecology and evolutionary biology of clonal plants: an introduction to the proceedings of Clone-2000. Evolutionary Ecology, 15: 223–230

    Article  Google Scholar 

  • Thompson F L, Eckert C G (2004). Trade-offs between sexual and clonal reproduction in an aquatic plant: experimental manipulations vs. phenotypic correlations. Journal of Evolution Biology, 17: 581–592

    Article  CAS  Google Scholar 

  • Thompson J D (2001). How do visitation patterns vary among pollinators in relation to floral display and floral design in a generalist pollination system? Oecologia, 126: 386–394

    Article  Google Scholar 

  • Ushimaru A, Kikuzawa K (1999). Variation of breeding system, floral rewards, and reproductive success in clonal Calystegia species (Convolvulaceae). American Journal of Botany, 86: 436–446

    Article  PubMed  Google Scholar 

  • Van Kleunen M, Fischer M (2001). Adaptive evolution of plastic foraging responses in a clonal plant. Ecology, 82: 3309–3319

    Article  Google Scholar 

  • Van Kleunen M, Fischer M, Schmid B (2001). Effects of intraspecific competition on size variation and reproductive allocation in a clonal plant. Oikos, 94: 515–524

    Article  Google Scholar 

  • Vange V (2002). Breeding system and inbreeding depression in the clonal plant species Knautia arvensis (Dipsacaceae): implications for survival in abandoned grassland. Biological Conservation, 108: 59–67

    Article  Google Scholar 

  • Watson A M, Casper B B (1984). Morphogenetic constraints on patterns of carbon distribution on plants. Annual Review of Ecology and Systematics, 15: 233–258

    Article  Google Scholar 

  • Westley L C (1993). The effect of inflorescence bud removal on tuber production in Helianthus tuberosus L.(Asteraceae). Ecology, 74: 2136–2144

    Article  Google Scholar 

  • Wilcock C C, Jennings S B (1999). Partner limitation and restoration of sexual reproduction in the clonal dwarf shrub Linnea borealis L.(Caprifoliaceae). Protoplasma, 208: 76–86

    Article  Google Scholar 

  • Williams G C (1966). Natural selection, the cost of reproduction and refinement of lacks of principle. American Naturalist, 100: 687–690

    Article  Google Scholar 

  • Winkler E, Fischer M (2001). The role of vegetative spread and seed dispersal for optimal life histories of clonal plants: a simulation study. Evolutionary Ecology, 15: 281–301

    Article  Google Scholar 

  • Wolf A T, Harrison S P (2001). Effects of habitat size and patch isolation on reproductive success of the serpentine morning glory. Conservation Biology, 15: 111–121

    Article  Google Scholar 

Download references

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Correspondence to Zhang Dayong.

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Translated from Acta Phytoecologica Sinica, 2006, 20(1): 174–183 [译自: 植物生态学报]

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Zhang, Y., Zhang, D. Asexual and sexual reproductive strategies in clonal plants. Front. Biol. China 2, 256–262 (2007). https://doi.org/10.1007/s11515-007-0036-0

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