Skip to main content

Fragmentation and the Role of Seed Banks in Promoting Persistence in Isolated Populations of Collinsia verna

  • Chapter
Book cover Conservation in Highly Fragmented Landscapes

Abstract

Plant species that inhabit environments characterized by environmental stochasticity and/or catastrophe have evolved two common bet-hedging strategies: one based on seed dispersal attributes and one on dormancy attributes, which lead to the formation of a soil seed bank. The environmental conditions that select for the evolution of spatial versus temporal dispersal will depend on both the magnitude of the environmental variance and the spatial array of suitable habitat patches. In species that normally are connected as a metapopulation, repeated local extinction occurs, and recolonization of the available habitat patches is accomplished by seed dispersal. In a metapopulation structure, individuals are distributed among a series of subpopulations that are connected to one another by dispersal. The number of individuals in each subpopulation fluctuates according to local demogrpahic conditions, and subpopulations can fluctuate largely independently. These fluctuations in numbers of individuals may periodically extirpate a subpopulation, but persistence of a species in such a subpopulation is enhanced because dispersing individuals from other subpopulations can recolonize an extirpated area. Thus metapopulation structure and function enhances the regional persistence of species in spatially and temporally variable environments (Hanski and Gilpin 1991). Spatiotemporal variability in subpopulation size and persistence probability favors the evolution of high dispersal rates among subpopulations (Gadgil 1971, Cohen and Levin 1991, den Boer 1987, McPeek and Holt 1992). High dispersal rates will enhance the persistence of the entire metapopulation by increasing the recolonization rate of extinct subpopulations (Hanski and Gilpin 1991, den Boer 1987, McPeek and Holt 1992, Ebenhard 1991, Verboom and Lankester 1991, Hanski 1991). However, if the distance among subpopulations exceeds the dispersal capacity of the organism and the probability of successful recolonization is low, the evolution of dormancy will be favored.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Bennington, C.C., J.B. McGraw, and M.C. Vavrek. 1991. Ecological genetic variation in seed banks. II. Phenotypic and genetic differences between young and old subpopulations of Luzula parviflora. Journal of Ecology 79: 627–643.

    Google Scholar 

  • Binder, B.J., and D.M. Anderson. 1990. Biochemical composition and metabolic activity of Scrippsiella trochoidea (Dinophyceae) resting cysts. Journal of Phycology, 26: 289–298.

    Article  Google Scholar 

  • Brown, J.S., and D.L. Venable. 1986. Evolutionary ecology of seed-bank annuals in temporally varying environments. American Naturalist 127 (1): 31–47.

    Article  Google Scholar 

  • Chesson, P.L. 1983. Coexistence of competitors in a stochastic environment: the storage effect. In H.I. Freedman, and C. Strobeck, eds. Population Biology. Lecture Notes in Biomathematics no. 52, Springer-Verlag, Berlin, 188–198.

    Google Scholar 

  • Chesson, P.L. 1984. The storage effect in stochastic population models. In S.A. Levin, and T.G. Hallum, eds. Mathematical Ecology. Lecture Notes in Biomathematics no. 54. Springer-Verlag, Berlin, 76–89.

    Google Scholar 

  • Chesson, P.L. 1985. Coexistence of competitors in spatially and temporally varying environments: A look at the combined effects of different sorts of variability. Theoretical Population Biology 28: 263–287.

    Article  Google Scholar 

  • Cohen, D. 1966. Optimizing reproduction in a randomly varying environment. Journal of Theoretical Biology 12: 119–129.

    Article  Google Scholar 

  • Cohen, D. 1967. Optimizing reproduction in a randomly varying environment when a correlation exists between the conditions at the time a choice has to be made and the subsequent outcome. Journal of Theoretical Biology 16: 1–14.

    Article  Google Scholar 

  • Cohen, D., and S.A. Levin. 1991. Dispersal in patchy environments: The effects of temporal and spatial structure. Theoretical Population Biology 39: 63–99.

    Article  Google Scholar 

  • De Mauro, M.M. 1993. Relationship of breeding system to rarity in the lakeside daisy (Hymenoxys acaulis var. glabra). Conservation Biology 7: 542–550.

    Article  Google Scholar 

  • Del Castillo, R.F. 1994. Factors influencing the genetic structure of Phacelia dubia, a species with a seed bank and large fluctuations in population size. Heredity 72: 446–458.

    Article  Google Scholar 

  • den Boer, P.J. 1987. Spreading the risk and stabilization of animal numbers. Acta Biotheoretica 18: 165–194.

    Article  Google Scholar 

  • DeStasio, B.T. 1989. The seed bank of a freshwater crustacean: copepodology for the plant ecologist. Ecology 70: 1377–1389.

    Article  Google Scholar 

  • Dingle, H. 1978. Migration and diapause in tropical, temperate, and island milkweed bugs. In H. Dingle, ed. Evolution of Insect Migration and Diapause. Springer, New York.

    Chapter  Google Scholar 

  • Edenhard, T. 1991. Colonization in metapopulations: A review of theory and observations. Biological Journal of the Linnean Society 42: 105–121.

    Article  Google Scholar 

  • Ellner, S. 1985a. ESS germination strategies in randomly varying environments. I. Logistic-type models. Theoretical Population Biology 28: 50–79.

    Article  Google Scholar 

  • Ellner, S. 1985b. ESS germination strategies in randomly varying environments. II. Reciprocal yield-law models. Theoretical Population Biology 28: 80–116.

    Article  Google Scholar 

  • Ellner, S., and N.G. Hairston. 1994. Role of overlapping generations in maintaining genetic variation in a fluctuating environment. American Naturalist 143: 403–417.

    Article  Google Scholar 

  • Epling, C., H. Lewis, and F.M. Ball. 1960. The breeding group and seed storage: A study in population dynamics. Evolution 14: 238–255.

    Article  Google Scholar 

  • Falconer, D.S. 1989. Introduction to Quantitative Genetics. 3rd ed. Longman, New York.

    Google Scholar 

  • Gabriel, W., and R. Burger. 1992. Survival of small populations under demographic stochasticity. Theoretical Population Biology 41: 44–71.

    Article  Google Scholar 

  • Gadgil, M. 1971. Dispersal: population consequences and evolution. Ecology 52: 253–261.

    Article  Google Scholar 

  • Gomulkiewicz, R., and R.D. Holt. 1995. When does evolution by natural selection prevent extinction? Evolution 49 (1): 201–207.

    Article  Google Scholar 

  • Gottlieb, L.D. 1974. Genetic stability in a peripheral isolate of Stephanomeria exigua spp. coronaria that fluctuates in population size. Genetics 76: 551–556.

    Google Scholar 

  • Greenlee, J.K., and K.S. Rai. 1986. Population differentiation in Collinsia verna. Nuttal (Scrophulariaceae): A multifaceted approach. Genetica 71:51–61.

    Google Scholar 

  • Greenlee, J.K., K.S. Rai, and A.D. Floyd. 1984. Intraspecific variation in nuclear DNA content in Collinsia verna Nutt. (Scrophulariaceae). Heredity 52: 235–242.

    Article  Google Scholar 

  • Hairston, N.G., Jr. and B.T. De Stasio, Jr. 1988. Rate of evolution slowed by a dormant propagule pool. Nature 336: 239–242.

    Article  Google Scholar 

  • Hanski, I., and M. Gilpin. 1991. Metapopulation dynamics: Brief history and conceptual domain. Biological Journal of the Linnean Society 42: 3–16.

    Article  Google Scholar 

  • Hanski, I. 1991. Single species metapopulation dynamics: concepts, models and observations. Biological Journal of the Linnean Society 42: 17–38.

    Article  Google Scholar 

  • Holsinger, K.S. 1993. The evolutionary dynamics of fragmented plant populations. In P.M. Kareiva, J.G. Kingsolver, and R.B. Huey, eds. Biotic Interactions and Global Change. Sinauer Associates, Sunderland, Mass., 198–216.

    Google Scholar 

  • Huntly, N., and P.L. Chesson. 1989. Short-term instabilities and long-term community dynamics. Trends in Ecology and Evolution 4: 293–298.

    Article  Google Scholar 

  • Kalisz, S. 1991. Experimental determination of seed bank age structure in the winter annual Collinsia verna. Ecology 72 (2): 575–585.

    Google Scholar 

  • Kalisz, S., and M.A. McPeek. 1992. Demography of an age structured annual: Resampled projection matrices, elasticity analyses and seed bank effects. Ecology 73: 1082–1093.

    Article  Google Scholar 

  • Kalisz, S., and M.A. McPeek. 1993. Extinction dynamics, population growth and seed banks. An example using an age-structured annual. Oecologia 95: 314–320.

    Article  Google Scholar 

  • Klinkhamer, P.G.L., T.J. DeJong, J.A. Metz, and J.Val. 1987. Life history tactics of annual organisms: The joint effects of dispersal and delayed germination. Theoretical Population Biology 32: 127–156.

    Article  Google Scholar 

  • Kuno, E. 1981. Dispersal and the persistence of populations in unstable habitats: A theoretical note. Oecologia (Berlin) 49: 123–126.

    Google Scholar 

  • Lande, R. 1993. Risks of population extinction from demographic and environmental stochasticity and random catastrophes. American Naturalist 142: 911–927.

    Article  Google Scholar 

  • Leberg, P.L. 1992. Effects of population bottlenecks on genetic diversity as measured by allozyme electrophoresis. Evolution 46 (2): 477–494.

    Article  Google Scholar 

  • Leck, M.A., V.T. Parker, and R.L. Simpson. 1989. Ecology of Soil Seed Banks. Academic Press, San Diego, 462.

    Google Scholar 

  • Levin, D.A. 1990. The seed bank as a source of genetic novelty in plants. American Naturalist 135: 563–572.

    Article  Google Scholar 

  • Levin, S.A., Cohen, D., and Hastings, A. 1984. Dispersal strategies in patchy environments. Theoretical Population Biology 26: 165–191.

    Article  Google Scholar 

  • Levins, R. 1969. Dormancy as an adaptive strategy. Symposia of the Society for Experimental Biology 23: 1–10.

    Google Scholar 

  • Linhart, Y.B., and A.C. Premoli. 1994. Genetic variation in central and disjunct populations of Lilium parryi. Canadian Journal of Botany 72: 79–85.

    Article  Google Scholar 

  • Lynch, M., and R.S. Lande. 1993. Evolution and extinction in response to environmental change. In P.M. Kareiva, J.G. Kingsolver, and R.B. Huey, eds. Biotic Interactions and Global Change. Sinauer Associates, Sunderland, Mass., 234–250.

    Google Scholar 

  • McCauley, D.E. 1993. Genetic consequences of extinction and recolonization in fragmented habitats. In P.M. Kareiva, J.G. Kingsolver, and R.B. Huey, eds. Biotic Interactions and Global Change. Sinauer Associates, Sunderland, Mass., 217–233.

    Google Scholar 

  • MacDonald, N., and A.R. Watkinson. 1981. Models of an annual plant population with a seed bank. Journal of Theoretical Biology 93: 643–653.

    Article  Google Scholar 

  • McPeek, M.A. 1989. Differential dispersal tendencies among Enallagma damselflies (Odo-nata: Coenagrionidae) inhabiting different habitats. Oikos 56: 187–195.

    Article  Google Scholar 

  • McPeek, M.A., and R.D. Holt. 1992. The evolution of dispersal in spatially and temporally varying environments. American Naturalist 140: 1010–1027.

    Article  Google Scholar 

  • Mangel, M., and C. Tier. 1993a. Dynamics of metapopulations with demographic stochasticity and environmental catastrophes. Theoretical Population Biology 44: 1–31.

    Article  Google Scholar 

  • Mangel, M., and C. Tier. 1993b. A simple direct method for finding persistence times of populations and application to conservation problems. Proceedings of the National Academy of Science of the United States of America 90: 1083–1086.

    Article  Google Scholar 

  • Mangel, M., and C. Tier. 1994. Four facts every conservation biologist should know about persistence. Ecology 75: 607–614.

    Article  Google Scholar 

  • Meffe, G.K., and C.R. Carroll. 1994. Principles of Conservation Biology. Sinauer Associates, Sunderland, Mass.

    Google Scholar 

  • Menges, E.S. 1990. Population viability analysis for an endangered plant. Conservation Biology 4: 52–62.

    Article  Google Scholar 

  • Menges, E.S. 1992. Stochastic modeling of extinction in plant populations. In P.L. Fiedler, and S.K. Jain, eds. Conservation biology: the theory and practice of nature conservation, preservation and management. Chapman and Hall, New York, 253–276.

    Google Scholar 

  • Olesen, J.M., and S.K. Jain. 1994. D: Fragmented plant populations and their lost interactions. In V. Loeschcke, J. Tomiuk and S.K. Jain eds. Conservation Genetics. Birkhauser Verlag, Basel, 417–426.

    Chapter  Google Scholar 

  • Oliviere, I., D. Couvet, and P.H. Gouyon. 1990. The genetics of transient populations: Research at the metapopulation level. Trends in Ecology and Evolution 5 (7): 207–210.

    Article  Google Scholar 

  • Ouburg, N.J. 1993. Isolation, population size and extinction-the classical and metapopula-tional approach applied to vascular plants along the Dutch Rhine-system. Oikos 66: 298308.

    Google Scholar 

  • Phillipi, T. 1993. Bet-hedging germination of desert annuals: Beyond the first year. American Naturalist 142: 474–487.

    Article  Google Scholar 

  • Philippi, T., and J. Seger. 1989. Hedging one’s evolutionary bets, revisited. Trends in Ecology and Evolution 4: 41–44.

    Article  Google Scholar 

  • Rathcke, B. 1983. Competition and facilitation among plants for pollination. In L. Real, ed. Pollination Biology. Academic Press, Orlando, 305–329.

    Google Scholar 

  • Reese, M. 1994. Delayed germination of seeds: A look at the effects of adult longevity, the timing of reproduction and population age/stage structure. American Naturalist 144: 43–64.

    Article  Google Scholar 

  • Ricket, W.H. 1966. Wild Flowers of the United States. Vol. 1. Part 2. McGraw-Hill, New York, 401–402.

    Google Scholar 

  • Schneller, J.J. 1988. Spore bank. Dark germination and gender determination in Athyrium and Dryopteris: Results and implications for population biology of pteridophyta. Botanica Helvetica 98: 77–86.

    Google Scholar 

  • Schneller, J.J., C.H. Haufler, and T.A. Ranker. 1990. Antheridiogen and natural gametophyte populations. American Fern Journal 80: 143–152.

    Article  Google Scholar 

  • Seger, J., and H.J. Brockmann. 1987. What is bet hedging? Oxford Surveys in Evolutionary Biology 4: 182–211.

    Google Scholar 

  • Shaffer, M.L. 1981. Minimum population sizes for species conservation. BioScience 31: 131–134.

    Article  Google Scholar 

  • Silvertown, J. 1988. The demographic and evolutionary consequences of seed dormancy. In A.J. Davy, M.J. Hutchings, and A.R. Watkinson, eds. Plant Population Ecology. Blackwell Scientific Publications, Oxford.

    Google Scholar 

  • Templeton, A.R., and D.A. Levin. 1979. Evolutionary consequences of seed pools. American Naturalist 114: 232–249.

    Article  Google Scholar 

  • Thiede, D.A. 1996. An Empirical Examination of Evolutionary Models of Maternal Effects. Ph.D. thesis. Michigan State University.

    Google Scholar 

  • Tonsor, S.J., S. Kalisz, J. Fisher, and T.P. Holtsford. 1993. A life-history based study of population genetic structure: Seed bank to adults in Plantago lanceolata. Evolution 47: 833–843.

    Article  Google Scholar 

  • Tscharntke, T. 1992. Fragmentation of Phragmites habitats, minimum viable population size, habitat suitability, and local extinction of moths, midges, flies, aphids, and birds. Conservation Biology 6 (4): 530–535.

    Article  Google Scholar 

  • Tuljapurkar, S.D. 1989. An uncertain life: Demography in random environments. Theoretical Population Biology 35: 227–294.

    Article  Google Scholar 

  • Vavrek, M.C., J.B. McGraw and C.C. Bennington. 1991. Ecological genetic variation in seed banks. III. Phenotypic and genetic differences between young and old seed populations of Carex bigelowii. Journal of Ecology 79: 645–662.

    Google Scholar 

  • Venable, D.L. 1985. The evolutionary ecology of seed heteromorphism. American Naturalist 126: 577–595.

    Article  Google Scholar 

  • Venable, D.L., and L. Lawlor. 1980. Delayed germination and escape in desert annuals: Escape in space and time. Oecologia 46: 272–282.

    Article  Google Scholar 

  • Verboom, J., and K. Lankester. 1991. Linking local and regional dynamics in stochastic metapopulation models. Biological Journal of the Linnean Society 42: 39–55.

    Article  Google Scholar 

  • Westoby, M. 1981. How diversified seed germination behavior is selected. American Naturalist 118: 882–885.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1997 Chapman & Hall

About this chapter

Cite this chapter

Kalisz, S., Horth, L., Mcpeek, M.A. (1997). Fragmentation and the Role of Seed Banks in Promoting Persistence in Isolated Populations of Collinsia verna . In: Schwartz, M.W. (eds) Conservation in Highly Fragmented Landscapes. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-0656-7_13

Download citation

  • DOI: https://doi.org/10.1007/978-1-4757-0656-7_13

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-0658-1

  • Online ISBN: 978-1-4757-0656-7

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics