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Biological Invasions

, Volume 21, Issue 1, pp 37–58 | Cite as

Tall-statured grasses: a useful functional group for invasion science

  • Susan CanavanEmail author
  • Laura A. Meyerson
  • Jasmin G. Packer
  • Petr Pyšek
  • Noëlie Maurel
  • Vanessa Lozano
  • David M. Richardson
  • Giuseppe Brundu
  • Kim Canavan
  • Angela Cicatelli
  • Jan Čuda
  • Wayne Dawson
  • Franz Essl
  • Francesco Guarino
  • Wen-Yong Guo
  • Mark van Kleunen
  • Holger Kreft
  • Carla Lambertini
  • Jan Pergl
  • Hana Skálová
  • Robert J. Soreng
  • Vernon Visser
  • Maria S. Vorontsova
  • Patrick Weigelt
  • Marten Winter
  • John R. U. Wilson
Review

Abstract

Species in the grass family (Poaceae) have caused some of the most damaging invasions in natural ecosystems, but plants in this family are also among the most widely used by humans. Therefore, it is important to be able to predict their likelihood of naturalisation and impact. We explore whether plant height is of particular importance in determining naturalisation success and impact in Poaceae by comparing naturalisation of tall-statured grasses (TSGs; defined as grass species that maintain a self-supporting height of 2 m or greater) to non-TSGs using the Global Naturalised Alien Flora database. We review the competitive traits of TSGs and collate risk assessments conducted on TSGs. Of the c. 11,000 grass species globally, 929 qualify (c. 8.6%) as TSGs. 80.6% of TSGs are woody bamboos, with the remaining species scattered among 21 tribes in seven subfamilies. When all grass species were analysed, TSGs and non-TSGs did not differ significantly in the probability of naturalisation. However, when we analysed woody bamboos separately from the other grasses, the percentage of TSGs that have naturalised was 2–4 times greater than that of non-TSGs for both bamboos and non-bamboo groups. Our analyses suggest that woody bamboos should be analysed separately from other TSGs when considering naturalisation; within the ≥ 2 m height class they do not naturalise at the same rate as other TSGs. Rapid growth rate and the capacity to accumulate biomass (a function of height) give many TSGs a competitive advantage and allow them to form monospecific stands, accumulate dense and deep litter mats, reduce light availability at ground level, and alter fire and nutrient-cycling regimes, thereby driving rapid ecosystem transformation. While the height distribution in grasses is continuous (i.e. no obvious break is evident in heights), the 2 m designation for TSGs defines an important functional group in grasses that can improve predictive modelling for management and biosecurity.

Keywords

Arundo Bamboos Biological invasions Height Invasive species Miscanthus Phragmites Plant functional groups Poaceae Risk assessment 

Notes

Acknowledgements

We thank the University of Sassari, Italy, for hosting the PhragNet 2016 planning meeting and creating the space that facilitated this manuscript. SC, DMR and JRUW acknowledge support from the DST-NRF Centre of Excellence for Invasion Biology and the National Research Foundation of South Africa (Grant 85417 to DMR). SC and JRUW acknowledge support from the South African National Department of Environment Affairs through its funding of the South African National Biodiversity Institute Invasive Species Programme. PP, JP, JČ, WYG and HS were supported by long-term research development Project RVO 67985939 (The Czech Academy of Sciences), Projects No. 14-36079G, Centre of Excellence PLADIAS and No. 14-15414S (Czech Science Foundation) and PP acknowledges support by Praemium Academiae award from The Czech Academy of Sciences. MvK and MW acknowledge support from the German Research Foundation (DFG, MvK: 264740629; MW: FZT 118), and FE was supported by the Austrian Science Foundation (FWF, Grant I2086-B16). JGP acknowledges support from the Faculty of Sciences and Environment Institute (Travel Grant 13116630) of The University of Adelaide.

Supplementary material

10530_2018_1815_MOESM1_ESM.docx (49 kb)
Supplementary material 1 (DOCX 49 kb)
10530_2018_1815_MOESM2_ESM.xls (102 kb)
Supplementary material 2 (XLS 101 kb)

References

  1. Ahmad R, Liow P-S, Spencer DF, Jasieniuk M (2008) Molecular evidence for a single genetic clone of invasive Arundo donax in the United States. Aquat Bot 88:113–120Google Scholar
  2. Amougou N, Bertrand I, Machet J-M, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus × giganteus, as affected by harvest date and N fertilization. Plant Soil 338:83–97Google Scholar
  3. Amougou N, Bertrand I, Cadoux S, Recous S (2012) Miscanthus × giganteus leaf senescence, decomposition and C and N inputs to soil. GCB Bioenergy 4:698–707Google Scholar
  4. Angeloni NL, Jankowski KJ, Tuchman NC, Kelly JJ (2006) Effects of an invasive cattail species (Typha × glauca) on sediment nitrogen and microbial community composition in a freshwater wetland. FEMS Microbiol Lett 263:86–92Google Scholar
  5. Bai S, Zhou G, Wang Y, Liang Q, Chen J, Cheng Y, Shen R (2013) Plant species diversity and dynamics in forests invaded by Moso bamboo (Phyllostachys edulis) in Tianmu Mountain Nature Reserve. Biodivers Sci 21:288–295Google Scholar
  6. Bates D, Mächler M, Bolker B, Walker S (2015) Fitting linear mixed-effects models using lme4. J Stat Softw 67:1–48Google Scholar
  7. Belzile F, Labbe J, LeBlanc MC, Lavoie C (2010) Seeds contribute strongly to the spread of the invasive genotype of the common reed (Phragmites australis). Biol Invasions 12:2243–2250Google Scholar
  8. Blanchard R, Kumschick S, Richardson DM (2017) Biofuel plants as potential invasive species: environmental concerns and progress towards objective risk assessment. In: Ruppel OC, Dix H (eds) Roadmap for sustainable biofuels in southern Africa: regulatory frameworks for improved development?, 1st edn. Nomos Verlagsgesellschaft mbH & Co. KG, Baden-Baden, pp 47–60Google Scholar
  9. Bonnett G, Kushner J, Saltonstall K (2014) The reproductive biology of Saccharum spontaneum L.: implications for management of this invasive weed in Panama. NeoBiota 20:61Google Scholar
  10. Bossard CC, Randall JM, Hshousky MC (2000) Invasive plants of California’s wildlands. University of California, BerkeleyGoogle Scholar
  11. Bouton JH (2007) Molecular breeding of switchgrass for use as a biofuel crop. Curr Opin Genet Dev 17:553–558Google Scholar
  12. Brooks ML, D’Antonio CM, Richardson DM, Grace JB, Keeley JE, DiTomaso JM, Hobbs RJ, Pellant M, Pyke D (2004) Effects of invasive alien plants on fire regimes. Bioscience 54:677–688Google Scholar
  13. Buddenhagen CE, Chimera C, Clifford P (2009) Assessing biofuel crop invasiveness: a case study. PLoS ONE 4:e5261Google Scholar
  14. Canavan K, Paterson ID, Hill MP (2017a) Exploring the origin and genetic diversity of the giant reed, Arundo donax in South Africa. Invasive Plant Sci Manag 10:53–60Google Scholar
  15. Canavan S, Richardson DM, Visser V, Roux JJL, Vorontsova MS, Wilson JRU (2017b) The global distribution of bamboos: assessing correlates of introduction and invasion. AoB Plants 9:plw078Google Scholar
  16. Canavan S, Kumschick S, Le Roux JJ, Richardson DM, Wilson JRU (2018a) Does origin determine environmental impacts? Not for bamboos. Plants People Planet.  https://doi.org/10.1002/ppp3.5
  17. Canavan K, Paterson ID, Lambertini C, Hill MP (2018b) Expansive reed populations-alien invasion or disturbed wetlands? AoB Plants 10:ply014Google Scholar
  18. Chambers RM, Meyerson LA, Saltonstall K (1999) Expansion of Phragmites australis into tidal wetlands of North America. Aquat Bot 64:261–273Google Scholar
  19. Chen J, Shafi M, Li S, Wang Y, Wu J, Ye Z, Peng D, Yan W, Liu D (2015) Copper induced oxidative stresses, antioxidant responses and phytoremediation potential of Moso bamboo (Phyllostachys pubescens). Sci Rep 5:13554Google Scholar
  20. Coffman GC, Ambrose RF, Rundel PW (2010) Wildfire promotes dominance of invasive giant reed (Arundo donax) in riparian ecosystems. Biol Invasions 12:2723–2734Google Scholar
  21. Colautti RI, Lau JA (2015) Contemporary evolution during invasion: evidence for differentiation, natural selection, and local adaptation. Mol Ecol 24:1999–2017Google Scholar
  22. Colautti RI, Grigorovich IA, MacIsaac HJ (2006) Propagule pressure: a null model for biological invasions. Biol Invasions 8:1023–1037Google Scholar
  23. Corneli E, Dragoni F, Adessi A, De Philippis R, Bonari E, Ragaglini G (2016) Energy conversion of biomass crops and agroindustrial residues by combined biohydrogen/biomethane system and anaerobic digestion. Bioresour Technol 211:509–518Google Scholar
  24. Cosentino SL, Copani V, D’Agosta GM, Sanzone E, Mantineo M (2006) First results on evaluation of Arundo donax L. clones collected in Southern Italy. Ind Crops Prod 23:212–222Google Scholar
  25. Cousens R (2008) Risk assessment of potential biofuel species: an application for trait-based models for predicting weediness? Weed Sci 56:873–882Google Scholar
  26. Czakó M, Feng X, He Y, Liang D, Márton L (2005) Genetic modification of wetland grasses for phytoremediation. Zeitschrift für Naturforschung 60c:285Google Scholar
  27. Dansereau P (1951) Description and recording of vegetation upon a structural basis. Ecology 32:172–229Google Scholar
  28. D’Antonio CM, Vitousek PM (1992) Biological invasions by exotic grasses, the grass/fire cycle, and global change. Annu Rev Ecol Syst 23:63–87Google Scholar
  29. de Kroon H, Kalliola R (1995) Shoot dynamics of the giant grass Gynerium sagittatum in Peruvian Amazon floodplains, a clonal plant that does show self-thinning. Oecologia 101:124–131Google Scholar
  30. Dehnen-Schmutz K, Touza J, Perrings C, Williamson M (2007) A century of the ornamental plant trade and its impact on invasion success. Divers Distrib 13:527–534Google Scholar
  31. DeMalach N, Zaady E, Weiner J, Kadmon R (2016) Size asymmetry of resource competition and the structure of plant communities. J Ecol 104:899–910Google Scholar
  32. Díaz S, Cabido M (1997) Plant functional types and ecosystem function in relation to global change. J Veg Sci 8:463–474Google Scholar
  33. Domènech R, Vilà M, Gesti J, Serrasolses I (2006) Neighbourhood association of Cortaderia selloana invasion, soil properties and plant community structure in Mediterranean coastal grasslands. Acta Oecol 29:171–177Google Scholar
  34. Dougherty RF (2013) Ecology and niche characterization of the invasive ornamental grass Miscanthus sinensis. Plant Pathology, Physiology, and Weed Science. Virginia Tech, Virginia TechGoogle Scholar
  35. Drewitz JJ, DiTomaso JM (2004) Seed biology of jubatagrass (Cortaderia jubata). Weed Sci 52:525–530Google Scholar
  36. Dwire KA, Kauffman JB (2003) Fire and riparian ecosystems in landscapes of the western USA. For Ecol Manag 178:61–74Google Scholar
  37. Ecker G, Zalapa J, Auer C (2015) Switchgrass (Panicum virgatum L.) genotypes differ between coastal sites and inland road corridors in the Northeastern US. PLoS ONE 10:e0130414Google Scholar
  38. Edwards D (1983) A broad-scale structural classification of vegetation for practical purposes. Bothalia 14:705–712Google Scholar
  39. Farrelly D (1984) The book of bamboo: a comprehensive guide to this remarkable plant, its uses, and its history. Thames and Hudson Ltd, LondonGoogle Scholar
  40. Farrer EC, Goldberg DE (2009) Litter drives ecosystem and plant community changes in cattail invasion. Ecol Appl 19:398–412Google Scholar
  41. Fischer T, Byerlee D, Edmeades G (2014) Crop yields and global food security: Will yield increase continue to feed the world? In: (ACIAR) TACfIAR (ed). Grains Research & Development Corporation (GRDC), Canberra, pp xxii + 634Google Scholar
  42. Flory SL, Lorentz KA, Gordon DR, Sollenberger LE (2012) Experimental approaches for evaluating the invasion risk of biofuel crops. Environ Res Lett 7:045904Google Scholar
  43. Fournier DA, Skaug HJ, Ancheta J, Ianelli J, Magnusson A, Maunder MN, Nielsen A, Sibert J (2012) AD Model Builder: using automatic differentiation for statistical inference of highly parameterized complex nonlinear models. Optim Methods Softw 27:233–249Google Scholar
  44. Foxcroft LC, Richardson DM, Wilson JRU (2008) Ornamental plants as invasive aliens: problems and solutions in Kruger National Park, South Africa. Environ Manag 41:32–51Google Scholar
  45. Gaertner M, Biggs R, Te Beest M, Hui C, Molofsky J, Richardson DM (2014) Invasive plants as drivers of regime shifts: identifying high-priority invaders that alter feedback relationships. Divers Distrib 20:733–744Google Scholar
  46. Gallagher RV, Randall RP, Leishman MR (2015) Trait differences between naturalized and invasive plant species independent of residence time and phylogeny. Conserv Biol 29:360–369Google Scholar
  47. Garnier E, Navas M-L (2012) A trait-based approach to comparative functional plant ecology: concepts, methods and applications for agroecology. A review. Agron Sustain Dev 32:365–399Google Scholar
  48. Garnier E, Stahl U, Laporte M-A, Kattge J, Mougenot I, Kühn I, Laporte B, Amiaud B, Ahrestani FS, Bönisch G, Bunker DE, Cornelissen JHC, Díaz S, Enquist BJ, Gachet S, Jaureguiberry P, Kleyer M, Lavorel S, Maicher L, Pérez-Harguindeguy N, Poorter H, Schildhauer M, Shipley B, Violle C, Weiher E, Wirth C, Wright IJ, Klotz S (2017) Towards a thesaurus of plant characteristics: an ecological contribution. J Ecol 105:298–309Google Scholar
  49. Gordon DR, Tancig KJ, Onderdonk DA, Gantz CA (2011) Assessing the invasive potential of biofuel species proposed for Florida and the United States using the Australian Weed Risk Assessment. Biomass Bioenergy 35:74–79Google Scholar
  50. Gordon-Gray KD, Ward CJ (1971) A contribution to knowledge of Phragmites (Gramineae) in South Africa, with particular reference to Natal populations. S Afr J Sci 37:1–30Google Scholar
  51. Grace JB (1993) The adaptive significance of clonal reproduction in angiosperms: an aquatic perspective. Aquat Bot 44:159–180Google Scholar
  52. Grime JP, Hodgson JG, Hunt RJ (1988) Comparative plant ecology. A functional approach to common British species. Unwyn Hyman, LondonGoogle Scholar
  53. Hardion L, Verlaque R, Baumel A, Juin M, Vila B (2012) Revised systematics of Mediterranean Arundo (Poaceae) based on AFLP fingerprints and morphology. Taxon 61:1217–1226Google Scholar
  54. Hartman JC, Nippert JB, Orozco RA, Springer CJ (2011) Potential ecological impacts of switchgrass (Panicum virgatum L.) biofuel cultivation in the Central Great Plains, USA. Biomass Bioenergy 35:3415–3421Google Scholar
  55. Haslam SM (2010) A book of reed: (Phragmites australis (Cav.) Trin. ex Steudel, formerly Phragmites communis Trin, Forrest Text, Tresaith, UKGoogle Scholar
  56. Heaton EA, Dohleman FG, Long SP (2008) Meeting US biofuel goals with less land: the potential of Miscanthus. Glob Change Biol 14:2000–2014Google Scholar
  57. Herrera AM, Dudley TL (2003) Reduction of riparian arthropod abundance and diversity as a consequence of giant reed (Arundo donax) invasion. Biol Invasions 5:167–177Google Scholar
  58. Holdredge C, Bertness MD (2011) Litter legacy increases the competitive advantage of invasive Phragmites australis in New England wetlands. Biol Invasions 13:423–433Google Scholar
  59. Holmes PM, Richardson DM, Esler KJ, Witkowski ETF, Fourie S (2005) A decision-making framework for restoring riparian zones degraded by invasive alien plants in South Africa: review article. S Afr J Sci 101:553–564Google Scholar
  60. Isagi Y, Oda T, Fukushima K, Lian C, Yokogawa M, Kaneko S (2016) Predominance of a single clone of the most widely distributed bamboo species Phyllostachys edulis in East Asia. J Plant Res 129:21–27Google Scholar
  61. IUCN (2009) Guidance on biofuels and Invasive species. IUCN, GlandGoogle Scholar
  62. Jaiswal RK, Mukherjee S, Raju KD, Saxena R (2002) Forest fire risk zone mapping from satellite imagery and GIS. Int J Appl Earth Obs Geoinf 4:1–10Google Scholar
  63. Jakob K, Zhou F (2009) Genetic improvement of C4 grasses as cellulosic biofuel feedstocks. In Vitro Cell Dev Biol Plant 45:291–305Google Scholar
  64. Jung SJ, Kim SH, Chung IM (2015) Comparison of lignin, cellulose, and hemicellulose contents for biofuels utilization among 4 types of lignocellulosic crops. Biomass Bioenergy 83:322–327Google Scholar
  65. Kettenring KM, McCormick MK, Baron HM, Whigham DF (2011) Mechanisms of Phragmites australis invasion: feedbacks among genetic diversity, nutrients, and sexual reproduction. J Appl Ecol 48:1305–1313Google Scholar
  66. Küchler AW (1949) A physiognomic classification of vegetation. Ann Assoc Am Geogr 39:201–210Google Scholar
  67. Kueffer C, Pyšek P, Richardson DM (2013) Integrative invasion science: model systems, multi-site studies, focused meta-analysis and invasion syndromes. New Phytol 200:615–633Google Scholar
  68. Lambert AM, Dudley TL, Saltonstall K (2010) Ecology and impacts of the large-statured invasive grasses Arundo donax and Phragmites australis in North America. Invasive Plant Sci Manag 3:489–494Google Scholar
  69. Lambrinos JG (2000) The impact of the invasive alien grass Cortaderia jubata (Lemoine) Stapf on an endangered mediterranean type shrubland in California. Divers Distrib 6:217–231Google Scholar
  70. Larpkern P, Moe SR, Totland Ø (2011) Bamboo dominance reduces tree regeneration in a disturbed tropical forest. Oecologia 165:161–168Google Scholar
  71. Lavergne S, Molofsky J (2007) Increased genetic variation and evolutionary potential drive the success of an invasive grass. Proc Natl Acad Sci 104:3883–3888Google Scholar
  72. Lavorel S, McIntyre S, Landsberg J, Forbes TDA (1997) Plant functional classifications: from general groups to specific groups based on response to disturbance. Trends Ecol Evol 12:474–478Google Scholar
  73. Liese W, Köhl M (2015) Bamboo: the plant and its uses. Springer, BerlinGoogle Scholar
  74. Lieurance D, Cooper A, Young AL, Gordon DR, Flory SL (2018) Running bamboo species pose a greater invasion risk than clumping bamboo species in the continental United States. J Nat Conserv 43:39–45Google Scholar
  75. Lima RAF, Rother DC, Muler AE, Lepsch IF, Rodrigues RR (2012) Bamboo overabundance alters forest structure and dynamics in the Atlantic Forest hotspot. Biol Conserv 147:32–39Google Scholar
  76. Linder HP, Lehmann CER, Archibald S, Osborne CP, Richardson DM (2018) Global grass (Poaceae) success underpinned by traits facilitating colonization, persistence and habitat transformation. Biol Rev Camb Philos Soc 93:1125–1144Google Scholar
  77. Lishawa SC, Lawrence BA, Albert DA, Tuchman NC (2015) Biomass harvest of invasive Typha promotes plant diversity in a Great Lakes coastal wetland. Restor Ecol 23:228–237Google Scholar
  78. Maceda-Veiga A, Basas H, Lanzaco G, Sala M, de Sostoa A, Serra A (2016) Impacts of the invader giant reed (Arundo donax) on riparian habitats and ground arthropod communities. Biol Invasions 18:731–749Google Scholar
  79. McCormick MK, Kettenring KM, Baron HM, Whigham DF (2010) Spread of invasive Phragmites australis in estuaries with differing degrees of development: genetic patterns, Allee effects and interpretation. J Ecol 98:1369–1378Google Scholar
  80. McWilliams JD (2004) Arundo donax. Fire effects information system U.S. Department of Agriculture. Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory, MissoulaGoogle Scholar
  81. Meffin R (2013) Alien Brassica: variation in performance among and within species and locations. Lincoln University, LincolnGoogle Scholar
  82. Meyerson LA (2000) Ecosystem-level effects of invasive species: a Phragmites case study in two freshwater tidal marsh ecosystems on the Connecticut River. School of Forestry and Environmental Studies, Yale UniversityGoogle Scholar
  83. Meyerson LA (2013) Evidence for multiple introductions of Phragmites australis to North America: detection of a new non-native haplotype. Biol Invasions 15:2605–2608Google Scholar
  84. Meyerson LA, Chambers RM, Vogt KA (1999) The effects of Phragmites removal on nutrient pools in a freshwater tidal marsh ecosystem. Biol Invasions 1:129–136Google Scholar
  85. Meyerson LA, Saltonstall K, Windham L, Kiviat E, Findlay S (2000) A comparison of Phragmites australis in freshwater and brackish marsh environments in North America. Wetl Ecol Manag 8:89–103Google Scholar
  86. Meyerson LA, Viola DV, Brown RN (2010) Hybridization of invasive Phragmites australis with a native subspecies in North America. Biol Invasions 12:103–111Google Scholar
  87. Mirza N, Mahmood Q, Pervez A, Ahmad R, Farooq R, Shah MM, Azim MR (2010) Phytoremediation potential of Arundo donax in arsenic-contaminated synthetic wastewater. Bioresour Technol 101:5815–5819Google Scholar
  88. Mislevy P, Fluck RC (1992) Harvesting operations and energetics of tall grasses for biomass energy production: a case study. Biomass Bioenergy 3:381–387Google Scholar
  89. Montti L, Villagra M, Campanello PI, Gatti MG, Goldstein G (2014) Functional traits enhance invasiveness of bamboos over co-occurring tree saplings in the semideciduous Atlantic Forest. Acta Oecol Int J Ecol 54:36–44Google Scholar
  90. Moodley D, Geerts S, Richardson DM, Wilson JRU (2013) Different traits determine introduction, naturalization and invasion success in woody plants: proteaceae as a test case. PLoS ONE 8:e75078Google Scholar
  91. Novoa A, Le Roux JJ, Robertson MP, Wilson JRU, Richardson DM (2015) Introduced and invasive cactus species: a global review. AoB Plants 7:plu078Google Scholar
  92. O’Connor PJ, Covich AP, Scatena FN, Loope LL (2000) Non-indigenous bamboo along headwater streams of the Luquillo Mountains, Puerto Rico: leaf fall, aquatic leaf decay and patterns of invasion. J Trop Ecol 16:499–516Google Scholar
  93. Okada M, Ahmad R, Jasieniuk M (2007) Microsatellite variation points to local landscape plantings as sources of invasive pampas grass (Cortaderia selloana) in California. Mol Ecol 16:4956–4971Google Scholar
  94. Onimaru K, Yabe K (1996) Comparisons of nutrient recovery and specific leaf area variation between Carex lasiocarpa var. occultans and Carex thunbergii var. appendiculata with reference to nutrient conditions and shading by Phragmites australis. Ecol Res 11:139–147Google Scholar
  95. Packer JG, Meyerson LA, Richardson DM, Brundu G, Allen WJ, Bhattarai GP, Brix H, Canavan S, Castiglione S, Cicatelli A, Čuda J, Cronin JT, Eller F, Guarino F, Guo W-H, Guo X, Hierro JL, Lambertini C, Liu J, Lozano V, Mozdzer TJ, Skálová H, Villarreal D, Wang R-Q, Pyšek P (2017) Global networks for invasion science: benefits, challenges and guidelines. Biol Invasions 19:1081–1096Google Scholar
  96. Pagad S (2016) Bamboos and invasiveness- identifying which bamboo species pose a risk to the natural environment and what can be done to reduce this risk. INBAR Working Paper No.77. International Network for Bamboo and Rattan, Beijing, ChinaGoogle Scholar
  97. Pérez-Harguindeguy N, Díaz S, Garnier E, Lavorel S, Poorter H, Jaureguiberry P, Bret-Harte MS, Cornwell WK, Craine JM, Gurvich DE, Urcelay C, Veneklaas EJ, Reich PB, Poorter L, Wright IJ, Ray P, Enrico L, Pausas JG, de Vos AC, Buchmann N, Funes G, Quétier F, Hodgson JG, Thompson K, Morgan HD, ter Steege H, Sack L, Blonder B, Poschlod P, Vaieretti MV, Conti G, Staver AC, Aquino S, Cornelissen JHC (2016) Corrigendum to: new handbook for standardised measurement of plant functional traits worldwide. Aust J Bot 64:715–716Google Scholar
  98. Pokorny ML, Sheley RL, Zabinski CA, Engel RE, Svejcar TJ, Borkowski JJ (2005) Plant functional group diversity as a mechanism for invasion resistance. Restor Ecol 13:448–459Google Scholar
  99. Pyšek P, Richardson DM (2008) Traits associated with invasiveness in alien plants: Where do we stand? In: Nentwig W (ed) Biological invasions. Ecological studies (analysis and synthesis). Springer, Berlin, pp 97–125Google Scholar
  100. Pyšek P, Jarošík V, Hulme PE, Kühn I, Wild J, Arianoutsou M, Bacher S, Chiron F, Didžiulis V, Essl F, Genovesi P, Gherardi F, Hejda M, Kark S, Lambdon PW, Desprez-Loustau M-L, Nentwig W, Pergl J, Poboljšaj K, Rabitsch W, Roques A, Roy DB, Shirley S, Solarz W, Vilà M, Winter M (2010) Disentangling the role of environmental and human pressures on biological invasions across Europe. Proc Natl Acad Sci 107:12157–12162Google Scholar
  101. Pyšek P, Jarošík V, Hulme PE, Pergl J, Hejda M, Schaffner U, Vilà M (2012) A global assessment of invasive plant impacts on resident species, communities and ecosystems: the interaction of impact measures, invading species’ traits and environment. Glob Change Biol 18:1725–1737Google Scholar
  102. Pyšek P, Skálová H, Čuda J, Guo W-Y, Suda J, Doležal J, Kauzál O, Lambertini C, Lučanová M, Mandáková T, Moravcová L, Pyšková K, Brix H, Meyerson LA (2018) Small genome separates native and invasive populations in an ecologically important cosmopolitan grass. Ecology 99:79–90Google Scholar
  103. Quinn LD, Allen DJ, Stewart JR (2010) Invasiveness potential of Miscanthus sinensis: implications for bioenergy production in the United States. GCB Bioenergy 2:310–320Google Scholar
  104. Razanajatovo M, Maurel N, Dawson W, Essl F, Kreft H, Pergl J, Pyšek P, Weigelt P, Winter M, van Kleunen M (2016) Plants capable of selfing are more likely to become naturalized. Nat Commun 7:13313Google Scholar
  105. Richardson DM, Blanchard R (2011) Learning from our mistakes: minimizing problems with invasive biofuel plants. Curr Opin Environ Sustain 3:36–42Google Scholar
  106. Richardson DM, Holmes PM, Esler KJ, Galatowitsch SM, Stromberg JC, Kirkman SP, Pyšek P, Hobbs RJ (2007a) Riparian vegetation: degradation, alien plant invasions, and restoration prospects. Divers Distrib 13:126–139Google Scholar
  107. Richardson DM, Rundel PW, Jackson ST, Teskey RO, Aronson J, Bytnerowicz A, Wingfield MJ, Proches S (2007b) Human impacts in pine forests: past, present, and future. Annu Rev Ecol Evol Syst 38:275–297Google Scholar
  108. Rieger JP, Kreager DA (1989) Giant reed (Arundo donax): a climax community of the riparian zone. Protection, management, and restoration for the 1990’s. In: Proceedings of the California riparian systems conference. US Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station, Berkeley, California, pp 222–225Google Scholar
  109. Rohani S, Dullo B, Woudwijk W, de Hoop P, Kooijman A, Grootjans AP (2014) Accumulation rates of soil organic matter in wet dune slacks on the Dutch Wadden Sea islands. Plant Soil 380:181–191Google Scholar
  110. Rossiter NA, Setterfield SA, Douglas M, Hutley LB (2003) Testing the grass-fire cycle: alien grass invasion in the tropical savannas of northern Australia. Divers Distrib 9:169–176Google Scholar
  111. Rossiter-Rachor NA, Setterfield SA, Douglas MM, Hutley LB, Cook GD, Schmidt S (2009) Invasive (gamba grass) is an ecosystem transformer of nitrogen relations in Australian savanna. Ecol Appl 19(6):1546–1560Google Scholar
  112. Rother DC, Rodrigues RR, Pizo MA (2016) Bamboo thickets alter the demographic structure of Euterpe edulis population: a keystone, threatened palm species of the Atlantic forest. Acta Oecol 70:96–102Google Scholar
  113. Saltonstall K (2002) Cryptic invasion by a non-native genotype of the common reed, Phragmites australis, into North America. Proc Natl Acad Sci USA 99:2445–2449Google Scholar
  114. Saltonstall K, Lambert A, Meyerson LA (2010) Genetics and reproduction of common (Phragmites australis) and giant reed (Arundo donax). Invasive Plant Sci Manag 3:495–505Google Scholar
  115. Schnitzler A, Essl F (2015) From horticulture and biofuel to invasion: the spread of Miscanthus taxa in the USA and Europe. Weed Res 55:221–225Google Scholar
  116. Scurlock JMO, Dayton DC, Hames B (2000) Bamboo: an overlooked biomass resource? Biomass Bioenergy 19:229–244Google Scholar
  117. SFAPRC (2006) Statistics of forest resources in China (1999–2003). State Forestry Administration, China. http://www.forestry.gov.cn/portal/main/s/65/content-90.html (In Chinese)
  118. Sheley RL, James J (2010) Resistance of native plant functional groups to invasion by medusahead (Taeniatherum caput-medusae). Invasive Plant Sci Manag 3:294–300Google Scholar
  119. Singh AN, Singh JS (1999) Biomass, net primary production and impact of bamboo plantation on soil redevelopment in a dry tropical region. For Ecol Manag 119:195–207Google Scholar
  120. Smith MD, van Wilgen BW, Burns CE, Govender N, Potgieter ALF, Andelman S, Biggs HC, Botha J, Trollope WSW (2013) Long-term effects of fire frequency and season on herbaceous vegetation in savannas of the Kruger National Park, South Africa. J Plant Ecol 6:71–83Google Scholar
  121. Smith LL, Tekiela DR, Barney JN (2015) Predicting biofuel invasiveness: a relative comparison to crops and weeds. Invasive Plant Sci Manag 8:323–333Google Scholar
  122. Soderstrom TR, Calderon CE (1979) A commentary on the bamboos (Poaceae: Bambusoideae). Biotropica 11:161–172Google Scholar
  123. Soltis PS, Soltis DE (2000) The role of genetic and genomic attributes in the success of polyploids. Proc Natl Acad Sci USA 97:7051–7057Google Scholar
  124. Song Q-n LuH, Liu J, Yang J, G-y Yang, Q-p Yang (2017) Accessing the impacts of bamboo expansion on NPP and N cycling in evergreen broadleaved forest in subtropical China. Sci Rep 7:40383Google Scholar
  125. Soreng RJ, Peterson PM, Romaschenko K, Davidse G, Zuloaga FO, Judziewicz EJ, Filgueiras TS, Davis JI, Morrone O (2015) A worldwide phylogenetic classification of the Poaceae (Gramineae). J Syst Evol 53(2):117–137Google Scholar
  126. Stueffer JF, De Kroon H, During HJ (1996) Exploitation of environmental hetergeneity by spatial division of labor in a clonal plant. Funct Ecol 10:328–334Google Scholar
  127. Suzaki T, Nakatsubo T (2001) Impact of the bamboo Phyllostachys bambusoides on the light environment and plant communities on riverbanks. J For Res 6:81–86Google Scholar
  128. Tang Y, Washitani I, Tsuchiya T, Iwaki H (1990) Growth analysis of Quercus serrata seedlings within Miscanthus sinensis grass canopies differing in light availability. Ecol Res 5:367–376Google Scholar
  129. Teixeira JS, Oatham MP (2001) An investigation into the effect of bamboo on the surrounding vegetation in the arena forest reserve. The living world. J Trinidad Tobago Field Nat Club 13–20Google Scholar
  130. Thompson K, Hodgson JG, Tim CGR (1995) Native and alien invasive plants: more of the same? Ecography 18:390–402Google Scholar
  131. Thomson FJ, Moles AT, Auld TD, Kingsford RT (2011) Seed dispersal distance is more strongly correlated with plant height than with seed mass. J Ecol 99:1299–1307Google Scholar
  132. Tilman D (1982) Resource competition and community structure. Princeton University Press, PrincetonGoogle Scholar
  133. Tilman D, Knops J, Wedin D, Reich P, Ritchie M, Siemann E (1997) The influence of functional diversity and composition on ecosystem processes. Science 277:1300–1302Google Scholar
  134. Van Doninck K, Schon I, De Bruyn L, Martens K (2002) A general purpose genotype in an ancient asexual. Oecologia 132:205–212Google Scholar
  135. van Kleunen M, Stuefer JF (1999) Quantifying the effects of reciprocal assimilate and water translocation in a clonal plant by the use of steam-girdling. Oikos 85:135–145Google Scholar
  136. van Kleunen M, Johnson SD, Fischer M (2007) Predicting naturalization of southern African Iridaceae in other regions. J Appl Ecol 44:594–603Google Scholar
  137. van Kleunen M, Dawson W, Essl F, Pergl J, Winter M, Weber E, Kreft H, Weigelt P, Kartesz J, Nishino M, Antonova LA, Barcelona JF, Cabezas FJ, Cardenas D, Cardenas-Toro J, Castano N, Chacon E, Chatelain C, Ebel AL, Figueiredo E, Fuentes N, Groom QJ, Henderson L, Inderjit Kupriyanov A, Masciadri S, Meerman J, Morozova O, Moser D, Nickrent DL, Patzelt A, Pelser PB, Baptiste MP, Poopath M, Schulze M, Seebens H, Shu WS, Thomas J, Velayos M, Wieringa JJ, Pysek P (2015) Global exchange and accumulation of non-native plants. Nature 525:100–103Google Scholar
  138. van Kleunen M, Essl F, Perg J, Brundu G, Carboni M, Dullinger S, Early R, González-Moreno P, Groom QJ, Hulme PE, Kueffer C, Kühn I, Máguas C, Maurel N, Novoa A, Parepa M, Pyšek P, Seebens H, Tanner R, Touza J, Verbrugge L, Weber E, Dawson W, Kreft H, Weigelt P, Winter M, Klonner G, Talluto MV, Dehnen-Schmutz K (2018) The changing role of ornamental horticulture in alien plant invasions. Biol Rev 93(3):1421–1437Google Scholar
  139. Vilà M, Pujadas J (2001) Land-use and socio-economic correlates of plant invasions in European and North African countries. Biol Conserv 100:397–401Google Scholar
  140. Visser V, Wilson JRU, Fish L, Brown C, Cook GD, Richardson DM (2016) Much more give than take: South Africa as a major donor but infrequent recipient of invasive non-native grasses. Global Ecol Biogeogr 25:679–692Google Scholar
  141. Vorontsova MS, Clark LG, Dransfield J, Govaerts R, Baker WJ (2016) World checklist of bamboos and rattans. INBAR Technical Report No. 37. International Network of Bamboo & Rattan, Beijing, ChinaGoogle Scholar
  142. Wang J, Ge Y, Zhang CB, Bai Y, Du ZK (2013) Dominant functional group effects on the invasion resistance at different resource levels. PLoS ONE 8:e77220Google Scholar
  143. Wang Y, Bai S, Binkley D, Zhou G, Fang F (2016) The independence of clonal shoot’s growth from light availability supports moso bamboo invasion of closed-canopy forest. For Ecol Manag 368:105–110Google Scholar
  144. Wang Y-J, Müller-Schärer H, van Kleunen M, Cai A-M, Zhang P, Yan R, Dong B-C, Yu F-H (2017) Invasive alien plants benefit more from clonal integration in heterogeneous environments than natives. New Phytol 216:1072–1078Google Scholar
  145. Welker JM, Briske DD (1992) Clonal biology of the temperate, caespitose, Graminoid Schizachyrium scoparium: a synthesis with reference to climate change. Oikos 63:357–365Google Scholar
  146. Westoby M, Falster DS, Moles AT, Vesk PA, Wright IJ (2002) Plant ecological strategies: some leading dimensions of variation between species. Annu Rev Ecol Syst 33:125–159Google Scholar
  147. Xu Q-F, Jiang P-K, Wu J-S, Zhou G-M, Shen R-F, Fuhrmann JJ (2014) Bamboo invasion of native broadleaf forest modified soil microbial communities and diversity. Biol Invasions 17:433–444Google Scholar
  148. Young SL, Barney JN, Kyser GB, Jones TS, DiTomaso JM (2009) Functionally similar species confer greater resistance to invasion: implications for grassland restoration. Restor Ecol 17:884–892Google Scholar

Copyright information

© Springer Nature Switzerland AG 2018

Authors and Affiliations

  1. 1.Centre for Invasion Biology, Department of Botany and ZoologyStellenbosch UniversityMatielandSouth Africa
  2. 2.South African National Biodiversity InstituteKirstenbosch Research CentreClaremontSouth Africa
  3. 3.Department of Natural Resources ScienceThe University of Rhode IslandKingstonUSA
  4. 4.Environment InstituteThe University of AdelaideAdelaideAustralia
  5. 5.Department of Invasion Ecology, Institute of BotanyThe Czech Academy of SciencesPrůhoniceCzech Republic
  6. 6.Department of Ecology, Faculty of ScienceCharles UniversityPragueCzech Republic
  7. 7.Ecology, Department of BiologyUniversity of KonstanzConstanceGermany
  8. 8.Department of AgricultureUniversity of SassariSassariItaly
  9. 9.Department of Zoology and EntomologyRhodes UniversityGrahamstownSouth Africa
  10. 10.Department of Chemistry and Biology ‘‘A. Zambelli’’University of SalernoFiscianoItaly
  11. 11.Department of BiosciencesDurham UniversityDurhamUK
  12. 12.Division of Conservation, Vegetation and Landscape EcologyUniversity of ViennaViennaAustria
  13. 13.Zhejiang Provincial Key Laboratory of Plant Evolutionary Ecology and ConservationTaizhou UniversityTaizhouChina
  14. 14.Biodiversity, Macroecology and BiogeographyUniversity of GöttingenGöttingenGermany
  15. 15.Centre of Biodiversity and Sustainable Land Use (CBL)University of GöttingenGöttingenGermany
  16. 16.Department of BioscienceAarhus UniversityAarhus CDenmark
  17. 17.Department of Botany, National Museum of Natural HistorySmithsonian InstitutionWashingtonUSA
  18. 18.Department of Statistical Sciences, Statistics in Ecology, Environment and ConservationUniversity of Cape TownRondeboschSouth Africa
  19. 19.African Climate and Development InitiativeUniversity of Cape TownCape Town, RondeboschSouth Africa
  20. 20.Comparative Plant and Fungal BiologyRoyal Botanic Gardens, KewRichmond, SurreyUK
  21. 21.German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-LeipzigLeipzigGermany
  22. 22.Leipzig UniversityLeipzigGermany

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