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Barriers to invasive infilling by Brachypodium sylvaticum in Pacific Northwest forests

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Abstract

The success of invasive plants is often dependent on continued natural and anthropogenic habitat perturbations but it is less clear whether invasive species are capable of infiltrating undisturbed plant communities (range infilling). We studied the ecology of Brachypodium sylvaticum (slender false brome), a Eurasian bunchgrass that forms dense and expansive monocultures in forests of Oregon’s Willamette Valley with the objective of assessing its potential to infill undisturbed forests near the edge of its expanding range. Observations suggest that B. sylvaticum may be associated with sites that have a history of disturbance, but infestations appear to be spreading in forest understory habitats. We assessed the effects of leaf litter depth and texture (proportions of coniferous and deciduous litter) on seedling recruitment in the field and in a controlled experiment. Coniferous litter facilitated the establishment and growth while the presence of deciduous litter severely reduced B. sylvaticum recruitment. Survival and growth of established B. sylvaticum seedlings was highest in the coniferous litter. Leaf litter treatments contributed to the retention of soil moisture and seedlings had increased biomass and more tillering with deeper litter. Field surveys partially corroborated these results; recruitment occurs at the edge of existing B. sylvaticum populations where leaf litter depth is moderate, but B. sylvaticum is absent from regions of the understory characterized by deeper and less dense leaf litter. These results suggest that B. sylvaticum has the potential to invade native understory communities, but the progress of invasion will depend on the frequency and intensity of perturbations of the accumulated leaf litter.

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References

  • Ahlgren CE, Ahlgren IF (1981) Some effects of different forest litters on seed germination and growth. Can J For Res 11:710–714

    Article  Google Scholar 

  • Amatangelo KL, Dukes JS, Field CB (2008) Responses of a California annual grassland to litter manipulation. J Veg Sci 19:605–612

    Article  Google Scholar 

  • Baker AC, Murray BR (2010) Relationships between leaf-litter traits and the emergence and early growth of invasive Pinus radiata seedlings. Weed Res 50:586–596

  • Barbour MG, Burk JH, Pitts WD, Gilliam FS, Schwartz MW (1998) Terrestrial plant ecology. Benjamin/Cummings, Menlo Park

    Google Scholar 

  • Bartuszevige AM, Hrenko RL, Gorchov DL (2007) Effects of leaf litter on establishment, growth and survival of invasive plant seedlings in a deciduous forest. Am Midl Nat 158:472–477

    Article  Google Scholar 

  • Borchert MI, Davis FW, Michaelsen J, Oyler LD (1989) Interactions of factors affecting seedling recruitment of blue oak (Quercus douglasii) in California. Ecology 70:389–404

    Article  Google Scholar 

  • Brown DJ, Nowlin WH, Ozel E, Mali I, Episcopo D, Jones MC, Forstner MRJ (2014) Comparison of short term low, moderate, and high severity fire impacts to aquatic and terrestrial ecosystem components of a southern USA mixed pine/hardwood forest. For Ecol Manag 312:179–192

    Article  Google Scholar 

  • Cano L, Escarre J, Blanco-Moreno JM, Sans FX (2008) Assessing the effect of inbreeding and long-distance gene flow on the invasive potential of Senecio pterophorus (Asteraceae). Aust J Bot 56:539–549

    Article  Google Scholar 

  • Connell JH (1979) Intermediate disturbance hypothesis. Science 204:1345

    Article  CAS  PubMed  Google Scholar 

  • Davis MA, Grime JP, Thompson K (2000) Fluctuating resources in plant communities: a general theory of invasibility. J Ecol 88:528–534

    Article  Google Scholar 

  • Deutsch ES, Bork EW, Willms WD (2010) Separation of grassland litter and ecosite influences on seasonal soil moisture and plant growth dynamics. Plant Ecol 209:135–145

    Article  Google Scholar 

  • Dietz H, Edwards PJ (2006) Recognition that causal processes change during plant invasion helps explain conflicts in evidence. Ecology 87:1359–1367

    Article  PubMed  Google Scholar 

  • Drake JM, Lodge DM (2006) Allee effects, propagule pressure and the probability of establishment: risk analysis for biological invasions. Biol Invasions 8:365–375

    Article  Google Scholar 

  • Facelli JM, Pickett STA (1991) Plant litter—its dynamics and effects on plant community structure. Bot Rev 57:1–32

    Article  Google Scholar 

  • Fowler NL (1986) Microsite requirements for germination and establishment of 3 grass species. Am Midl Nat 115:131–145

    Article  Google Scholar 

  • Fowler NL (1988) What is a safe site—neighbor, litter, germination date, and patch effects. Ecology 69:947–961

    Article  Google Scholar 

  • Fox BJ, Fox MD, Taylor JE, Jackson GP, Simpson J, Higgs P, Rebec L, Avery R (1996) Comparison of regeneration following burning, clearing or mineral sand mining at Tomago, NSW.1. Structure and growth of the vegetation. Aust J Ecol 21:184–199

    Article  Google Scholar 

  • Harper JL (1967) A Darwinian approach to plant ecology. J Ecol 55:247–270

    Article  Google Scholar 

  • Holmes SE, Roy BA, Reed JP, Johnson BJ (2010) Context-dependent pattern and process: the distribution and competitive dynamics of an invasive grass Brachypodium sylvaticum. Biol Invasions 12:2302–2318

    Article  Google Scholar 

  • Hull AJC (1974) Species for seeding mountain rangelands in Southeastern Idaho, Northeastern Utah, and Western Wyoming. J Range Manag 27:150–153

    Article  Google Scholar 

  • Johnstone IM (1986) Plant invasion windows: a time-based classification of invasion potential. Biol Rev 61:369–394

    Article  Google Scholar 

  • Kaye T (2003) Invasive plant alert: false brome (Brachypodium sylvaticum). Institute for Applied Ecology, False Brome Working Group, Corvallis

    Google Scholar 

  • Kaye TN, Blakeley-Smith M (2006) False-brome (Brachypodium sylvaticum). In: Boersma PD, Reichard SE, van Buren AN (eds) Invasive species in the Pacific Northwest. University of Washington Press, Seattle, pp 80–81

    Google Scholar 

  • Knapp AK, Seastedt TR (1986) Detritus accumulation limits productivity of tallgrass prairie. Bioscience 36:662–668

    Article  Google Scholar 

  • Kotanen PM, Bergelson J, Hazlett DL (1998) Habitats of native and exotic plants in Colorado shortgrass steppe: a comparative approach. Can J Bot 76:664–672

    Google Scholar 

  • Kumar R, Shahabuddin G (2005) Effects of biomass extraction on vegetation structure, diversity and composition of forests in Sariska Tiger Reserve India. Environ Conserv 32:248–259

    Article  Google Scholar 

  • Larson BMH, Catling PM, Waldron GE (2007) The biology of Canadian weeds. 135. Lonicera japonica Thunb. Can J Plant Sci 87:423–438

    Article  Google Scholar 

  • Lavergne S, Molofsky J (2004) Reed canary grass (Phalaris arundinacea) as a biological model in the study of plant invasions. Crit Rev Plant Sci 23:415–429

    Article  Google Scholar 

  • Lockwood JL, Cassey P, Blackburn T (2005) The role of propagule pressure in explaining species invasions. Trends Ecol Evol 20:223–228

    Article  PubMed  Google Scholar 

  • Miller NP, Matlack GR (2010) Population expansion in an invasive grass, Microstegium vimineum: a test of the channelled diffusion model. Divers Distrib 16:816–826

    Article  Google Scholar 

  • Mitchell CE, Agrawal AA, Bever JD, Gilbert GS, Hufbauer RA, Klironomos JN, Maron JL, Morris WF, Parker IM, Power AG, Seabloom EW, Torchin ME, Vazquez DP (2006) Biotic interactions and plant invasions. Ecol Lett 9:726–740

    Article  PubMed  Google Scholar 

  • Moloney KA, Knaus F, Dietz H (2009) Evidence for a shift in life-history strategy during the secondary phase of a plant invasion. Biol Invasions 11:625–634

    Article  Google Scholar 

  • Motzkin G, Wilson P, Foster DR, Allen A (1999) Vegetation patterns in heterogeneous landscapes: the importance of history and environment. J Veg Sci 10:903–920

    Article  Google Scholar 

  • Murchie EH, Horton P (1997) Acclimation of photosynthesis to irradiance and spectral quality in British plant species: chlorophyll content, photosynthetic capacity and habitat preference. Plant, Cell Environ 20:438–448

    Article  Google Scholar 

  • Oregonstateparks.org (2014) In http://www.oregonstateparks.org/index.cfm?do=parkPage.dsp_parkHistory&parkId=102

  • Ramakrishnan AP, Musial T, Cruzan MB (2010) Shifting dispersal modes at an expanding species’ range margin. Mol Ecol 19:1134–1146

  • Rosenthal DM, Ramakrishnan AP, Cruzan MB (2008) Evidence for multiple sources and intraspecific hybridization at early stages of the invasion of Brachypodium sylvaticum (Hudson) Beauv. in North America. Mol Ecol 17:4657–4669

    Article  PubMed  Google Scholar 

  • Roy BA (2010) Brachypodium sylvaticum invasive species compendium. CABI, Wellingford

    Google Scholar 

  • Roy BA, Güsewell S, Coulson T, Blaser W, Policha T, Stewart J, Blaisdell K (2011) Population regulation by enemies of the grass Brachypodium sylvaticum: demography in native and invaded ranges Ecology. Ecology 92:665–675

    Article  PubMed  Google Scholar 

  • SAS (2007) SAS/STAT user’s guide version 9.02. SAS institute, Carey

    Google Scholar 

  • Sayer EJ (2006) Using experimental manipulation to assess the roles of leaf litter in the functioning of forest ecosystems. Biol Rev 81:1–31

    Article  PubMed  Google Scholar 

  • Schramm JW, Ehrenfeld JG (2010) Leaf litter and understory canopy shade limit the establishment, growth and reproduction of Microstegium vimineum. Biol Invasions 12:3195–3204

    Article  Google Scholar 

  • Sloop CM, Ayres DR, Strong DR (2011) Spatial and temporal genetic structure in a hybrid cordgrass invasion. Heredity 106:547–556

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Spence LA, Ross JV, Wiser SK, Allen RB, Coomes DA (2011) Disturbance affects short-term facilitation, but not long-term saturation, of exotic plant invasion in New Zealand forest. Proc R Soc Lond Ser B Biol Sci 278:1457–1466

    Article  Google Scholar 

  • Stout JC (2007) Reproductive biology of the invasive exotic shrub, Rhododendron ponticum L. (Ericaceae). Bot J Linn Soc 155:373–381

    Article  Google Scholar 

  • Suarez ER, Fahey TJ, Yavitt JB, Groffman PM, Bohlen PJ (2006) Patterns of litter disappearance in a northern hardwood forest invaded by exotic earthworms. Ecol Appl 16:154–165

    Article  PubMed  Google Scholar 

  • Suehs CM, Affre L, Medail F (2004) Invasion dynamics of two alien Carpobrotus (Aizoaceae) taxa on a Mediterranean island: II. Reproductive strategies. Heredity 92:550–556

    Article  CAS  PubMed  Google Scholar 

  • Sydes C, Grime JP (1981a) Effects of tree leaf litter on herbaceous vegetation in deciduous woodland. 2. An experimental investigation. J Ecol 69:249–262

    Article  Google Scholar 

  • Sydes C, Grime JP (1981b) Effects of tree leaf litter on herbaceous vegetation in deciduous woodland. 1. Field investigations. J Ecol 69:237–248

    Article  Google Scholar 

  • Tanentzap AJ, Bazely DR, Lafortezza R (2010) Diversity-invasibility relationships across multiple scales in disturbed forest understoreys. Biol Invasions 12:2105–2116

    Article  Google Scholar 

  • Taylor LAV, Cruzan MB (2015) Propagule pressure and disturbance drive the invasion of perennial false brome (Brachypodium sylvaticum). Invasive Plant Sci Manag (in press)

  • Wangen SR, Webster CR (2006) Potential for multiple lag phases during biotic invasions: reconstructing an invasion of the exotic tree Acer platanoides. J Appl Ecol 43:258–268

    Article  Google Scholar 

  • Warren RJ, Ursell T, Keiser AD, Bradford MA (2013) Habitat, dispersal and propagule pressure control exotic plant infilling within an invaded range. Ecosphere. doi:10.1890/ES12-00393.1

    Google Scholar 

  • Weaver JE, Rowland NW (1952) Effects of excessive natural mulch on development, yield, and structure of native grassland. Bot Gaz 114:1–19

    Article  Google Scholar 

  • Xiong SJ, Nilsson C (1999) The effects of plant litter on vegetation: a meta-analysis. J Ecol 87:984–994

    Article  Google Scholar 

Download references

Acknowledgments

We thank the biology senior capstone students from the summer of 2010 (Emma Bell, James Choban, James Dunn, Ganaji Ganesh, Nina Jiminez, Naomi Scott, Jennifer Wetzold, Bianca Nettles, and Bram Stone) and 2012 (Emily Blue, Ryan Castro, Steven Heckethorn, Ashley Howell, Keeley Jensen, Roman Kondratyev, Caitlin Maraist, Kevin McWhirter, and Michelle Williamson) for assistance with data collection in the field. We also thank the staff and administrators of Milo McIver State Park for access to the property. Tanya Cheeke, Caitlin Lee, Rachael Workman, and two anonymous reviewers provided helpful feedback on a previous draft the manuscript.

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Correspondence to Mitchell B. Cruzan.

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Taylor, L.A.V., Hasenkopf, E.A. & Cruzan, M.B. Barriers to invasive infilling by Brachypodium sylvaticum in Pacific Northwest forests. Biol Invasions 17, 2247–2260 (2015). https://doi.org/10.1007/s10530-015-0871-x

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