Skip to main content
Log in

Disturbance, Herbivory, and Propagule Dispersal Control Dominance of an Invasive Grass

  • Published:
Biological Invasions Aims and scope Submit manuscript

Abstract

Despite the dramatic changes invasive plants cause to ecosystems and communities, factors that control dominance of invasive species after establishment in a community are poorly understood. Most active management relies on catastrophic disturbances of invasive-dominated communities to increase richness and diversity of plant communities. This study examines the importance of propagule dispersal and deer herbivory on continued dominance of Phalaris arundinacea after a non-catastrophic, short-term disturbance to monotypic stands of this invasive grass. The disturbance caused no change in P. arundinacea cover among treatments during any year of the study and, thus, simulates disturbance intensity more likely to be encountered in unmanaged settings. Despite the small disturbance, the combinations of disturbance + seeding and disturbance + seeding + deer exclusion caused greater species richness than controls even three years after disturbance. Increased invasion of P. arundinacea stands caused few effects on the dominant, as P. arundinacea biomass was unaffected after the first year. Selective herbivory by deer of species other than P. arundinacea increased the effects of disturbance and seeding, and aided in continued dominance of the grass. The tolerance of P. arundinacea for direct anthropogenic effects, including poor water quality and hydroperiod fluctuations, and indirect effects, such as increased herbivory by historically high deer populations, indicates the complexity of determining persistence of invasive species.

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

  • Adjei MB and Pitman WD (1993) Response of the temperate perennial grass, reed canarygrass, to defoliation on a peninsular Florida spodosol. Soil Crop Science Society of Florida Proceedings 52: 1–4

    Google Scholar 

  • Anderson R (1994) Height of white-flowered trillium (Trillium grandiflorum) as an index of deer browsing intensity. Ecological Applications 4: 104–109

    Google Scholar 

  • Augustine D and Frelich LE (1998) Effects of white-tailed deer grazing intensity on populations of an understory forb in fragmented deciduous forests. Conservation Biology 12: 995–1004

    Google Scholar 

  • Augustine D and McNaughton SJ (1998) Ungulate effects on the functional species composition of plant communities: herbivore selectivity and plant tolerance. Journal of Wildlife Management 62: 1165–1183

    Google Scholar 

  • Balgooyen C and Waller DM (1995) The use of Clintonia borealis and other indicators to guage impacts of white-tailed deer on plant communities in northern Wisconsin, USA. Natural Areas Journal 15: 308–318

    Google Scholar 

  • Baskin CC and Baskin JM (1998) Seeds: Ecology, Biogeography, and Evolution of Dormancy and Germination. Academic Press, San Diego

    Google Scholar 

  • Bosy JL and Reader RJ (1995) Mechanisms underlying the suppression of forb seedling emergence by grass (Poa pratensis) litter. Functional Ecology 9: 635–639

    Google Scholar 

  • Boutin C and Keddy PA(1993) Afunctional classification of wetland plants. Journal of Vegetation Science 4: 591–600

    Google Scholar 

  • Brabec J and Pysek P (2000) Establishment and survival of three invasive taxa of the genus Reynoutria (Polygonaceae) in mesic mown meadows: a field experimental study. Folia Geobotanica 35: 27–42

    Google Scholar 

  • Britton AJ, Carey PD, Pakeman RJ and Marrs RH (2000) A comparison of regeneration dynamics following gap creation at two geographically contrasting heathland sites. Journal of Applied Ecology 37: 832–844

    Google Scholar 

  • Brown SC (1998) Remnant seed banks and vegetation as predictors of restored marsh vegetation. Canadian Journal of Botany 76: 620–629

    Google Scholar 

  • Burke MJG and Grime JP (1996) An experimental study of plant community invasibility. Ecology 77: 776–790

    Google Scholar 

  • Clark DL and Wilson MV (2001) Fire, mowing, and hand-removal of woody species in restoring a native wetland prairie in the Willamette Valley of Oregon. Wetlands 21: 135–144

    Google Scholar 

  • Conchou O and Patou G (1987) Modes of colonization of an heterogeneous alluvial area on the edge of the Garrone River by Phalaris arundinacea. Regulated Rivers 1: 37–48

    Google Scholar 

  • Connell JH and Slatyer RO (1977) Mechanism of succession in natural communities and their role in community stability and organization. American Naturalist 111: 1119–1144

    Google Scholar 

  • Cross JR (1981) The establishment of Rhododendron ponticum in the Killarney oakwoods, s.w. Ireland. Journal of Ecology 69: 807–824

    Google Scholar 

  • Duncan KW and McDaniel KC (1998) Saltcedar (Tamarix spp.) management with imazapyr. Weed Technology 12: 337–344

    Google Scholar 

  • Dunn O (1964) Multiple contrasts using rank sums. Technometrics 6: 241–252

    Google Scholar 

  • Farnsworth E and Meyerson LA (1999) Species composition and inter-annual dynamics of a freshwater tidal plant community following removal of the invasive grass, Phragmites australis. Biological Invasions 1: 115–127

    Google Scholar 

  • Frame J and Morrison MW (1991) Herbage productivity of prairie grass, reed canarygrass and phalaris. Agronomy Journal 71: 627–630

    Google Scholar 

  • Galatowitsch SM and van der Valk AG (1994) Restoring Prairie Wetlands: An Ecological Approach. Iowa State University Press, Ames, Iowa

  • Galatowitsch SM and van der Valk AG(1995) Reference revegetation during restoration of wetlands in the southern prairie pothole region of North America. In: Wheeler BD, Shaw SC, Fojt WL and Robertson RA (eds) Restoration of Temperate Wetlands, 129–142. John Wiley and Sons, Chichester, UK

    Google Scholar 

  • Galatowitsch SM and van der Valk AG (1996a) Characteristics of recently restored wetlands in the prairie pothole region. Wetlands 16: 75–83

    Google Scholar 

  • Galatowitsch SM and van der Valk AG (1996b) The vegetation of restored and reference prairie wetlands. Ecological Applications 6: 102–112

    Google Scholar 

  • Galatowitsch SM, Anderson NO and Ascher PD (1999) Invasive-ness in wetland plants in temperate North America. Wetlands 19: 733–755

    Google Scholar 

  • Galatowitsch SM, Whited DC, Lehtinen R, Husveth J and Schik K (2000) The vegetation of wet meadows in relation to their land-use. Environmental Monitoring and Assessment 60: 121–144

    Google Scholar 

  • Gaudet CL and Keddy PA (1995) Competitive performance and species distribution in shoreline plant communities: a comparative approach. Ecology 76: 280–291

    Google Scholar 

  • Gross KL (1990) A comparison of methods for estimating seed numbers in the soil. Journal of Ecology 78: 1079–1093

    Google Scholar 

  • Kalkhan MA and Stohlgren TJ (2000) Using multi-scale sampling and spatial cross-correlation to investigate patterns of plant species richness. Environmental Monitoring and Assessment 64: 591–605

    Google Scholar 

  • Kellogg CH and Bridgham SD (2002) Colonization during early succession of restored freshwater marshes. Canadian Journal of Botany 80: 176–185

    Google Scholar 

  • Kellogg CH, Bridgham SD and Leicht SA (2003) Effects of water level, shade and time on germination and growth of freshwater marsh plants along a simulated successional gradient. Journal of Ecology 91: 274–282.

    Google Scholar 

  • King SE and Grace JB (2000) The effects of gap size and disturbance type on invasion of wet pine savanna by cogongrass, Imperata cylindrica (Poaceae). American Journal of Botany 87: 1279–1286

    Google Scholar 

  • Kolar CS and Lodge DM (2001) Progress in invasion biology: predicting invaders. Trends in Ecology and Evolution 16: 199–204

    Google Scholar 

  • Lee JS, Ahn JH, Jo IH and Kim DA (1996) Effects of cutting frequency and nitrogen fertilization on dry matter yield of reed canarygrass (Phalaris arundinacea L.) in uncultivated rice paddy. American Journal of Agricultural Science 9: 737–741

    Google Scholar 

  • Levine JM(2000) Species diversity and biological invasions: relating local process to community pattern. Science 288: 852–854

    Google Scholar 

  • Lodge DM (1993) Biological invasions: lessons for ecology. Trends in Ecology and Evolution 8: 133–137

    Google Scholar 

  • Marten GC and Heath ME (1985) Reed canarygrass. In: Heath ME, Barnes RF and Metcalfe DS (eds) Forages: the Science of Grassland Agriculture, 207–216. Iowa State University Press, Ames, Iowa

    Google Scholar 

  • Marten GC, Jordan RM and Hovin AW (1976) Biological significance of reed canary grass alkaloids and associated palatability variation to grazing sheep and cattle. Agronomy Journal 68: 909–913

    Google Scholar 

  • McIntyre S, Lavorel S and Tremont RM (1995) Plant life-history attributes: their relationship to disturbance responses in herbaceous vegetation. Journal of Ecology 83: 31–44

    Google Scholar 

  • McJannet CL, Keddy PA and Pick FR (1995) Nitrogen and phosphorus tissue concentrations in 41 wetland plants: a comparison across habitats and functional groups. Functional Ecology 9: 231–238

    Google Scholar 

  • Meyer AH and Schmid B (1999) Experimental demography of rhizome populations of establishing clones of Solidago altissima. Journal of Ecology 87: 42–54

    Google Scholar 

  • Morrison SL and Molofsky J (1999) Environmental and genetic effects on the early survival and growth of the invasive grass Phalaris arundinacea. Canadian Journal of Botany 77: 1447–1453

    Google Scholar 

  • Paveglio FL and Kilbride KM (2000) Response of vegetation to control of reed canarygrass in seasonally managed wetlands of southwestern Washington. Wildlife Society Bulletin 28: 730–740

    Google Scholar 

  • Pierce SM and Cowling RM (1991) Dynamics of soil-stored seed banks of six shrubs in fire-prone dune fynbos. Journal of Ecology 79: 731–747

    Google Scholar 

  • Reinartz JA and Warne EL (1993) Development of vegetation in small created wetlands in southeastern Wisconsin. Wetlands 13: 153–164

    Google Scholar 

  • Riemenschneider V, Cordell TB and Allison B (1995) Impact of white-tailed deer on plant cover and biomass in Potato Creek State Park, St. Joseph County, Indiana. Proceedings of the Indiana Academy of Science 104: 35–41

    Google Scholar 

  • Rooney T (1997) Escaping herbivory: refuge effects on the morphology and hoot demography of the forest clonal herb Maianthe-um canadense. Journal of the Torrey Botanical Society 124: 280–285

    Google Scholar 

  • Schmitz DC and Simberloff D (1997) Biological invasions: a growing threat. Issues in Science and Technology 13: 33–40

    Google Scholar 

  • Simberloff D and Von Holle B (1999) Positive interactions of non-indigenous species: pinvasional meltdown? Biological Invasions 1: 1–32

    Google Scholar 

  • Stadler J, Trefflich A, Klotz S and Brandl R (2000) Exotic plant species invade diversity hot spots: the alien flora of northwestern Kenya. Ecography 23: 169–176

    Google Scholar 

  • Stone CP (1985) Alien animals in Hawaii's native ecosystems: toward controlling the adverse effects of introduced vertebrates. In: Stone CP and Scott JM (eds) Hawaii's Terrestrial Ecosystems: Preservation and Management, 251–297. University of Hawaii, Honolulu, Hawaii

  • Symstad A (2000) A test of the effects of functional group richness and composition on grassland invasibility. Ecology 81: 99–109

    Google Scholar 

  • Tilman D (1993) Species richness of experimental productivity gradients: how important is colonization limitation? Ecology 74: 2179–2191

    Google Scholar 

  • Tilman D (1997) Community invasibility, recruitment limitation, and grassland biodiversity. Ecology 78: 81–92

    Google Scholar 

  • Ussery JG and Krannitz PG (1998) Control of Scot's broom (Cytisus scoparius (L.) Link.): the relative conservation merits of pulling versus cutting. Northwest Science 72: 268–273

    Google Scholar 

  • van der Valk AG, Bremholm TL and Gordon E (1999) The restoration of sedge meadows: seed viability, seed germination requirements, and seedling growth of Carex species. Wetlands 19: 756–764

    Google Scholar 

  • Vitousek PM (1990) Biological invasions and ecosystem processes: towards an integration of population biology and ecosystem studies. Oikos 57: 7–13

    Google Scholar 

  • Vitousek PM, D'Antonio CM, Loope LL and Westbrooks R (1996) Biological invasions as global environmental change. American Scientist 84: 468–478

    Google Scholar 

  • Voss E (1972) Michigan Flora: Part I. Cranbrook Press, Bloomfield Hills, Michigan

    Google Scholar 

  • Voss E (1985) Michigan Flora: Part II. Cranbrook Press, Bloomfield Hills, Michigan

    Google Scholar 

  • Voss E (1996) Michigan Flora: Part III. Cranbrook Press, Bloomfield Hills, Michigan

    Google Scholar 

  • Williamson M (1996) Biological Invasions. T.J. Press, Padstow, UK

    Google Scholar 

  • Zar J (1999) Biostatistical Analysis. 4th edn. Prentice-Hall, Upper Saddle River, New Jersey

    Google Scholar 

  • Zeiders KE and Sherwood RT (1985) Environmental interactions among reed canarygrass genotypes for nutritive value, height and disease severity. Agronomy Journal 77: 94–98

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Chev H. Kellogg.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kellogg, C.H., Bridgham, S.D. Disturbance, Herbivory, and Propagule Dispersal Control Dominance of an Invasive Grass. Biological Invasions 6, 319–329 (2004). https://doi.org/10.1023/B:BINV.0000034606.84830.d5

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:BINV.0000034606.84830.d5

Navigation