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An ecological comparison of Impatiens glandulifera Royle in the native and introduced range

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Abstract

Understanding the ecology of plant species in their whole range (native and introduced) can provide insights into those that become problematic weeds in the introduced range despite being benign components of the vegetative community in the native range. We studied the morphological traits of Impatiens glandulifera in the native (Indian Himalayas) and introduced (UK) range and evaluated what influences natural enemies and arbuscular mycorrhizal fungi (AMF) have on plant performance. We compared height, total leaf area, root: shoot ratio, natural enemy damage and the colonisation of AMF from individual plants within and between ranges twice in 2010 during the months of June and August. In addition, in August 2010, we estimated the number of reproductive units (expressed as the sum of flowers, seed capsule and seeds) at each site. We found that all morphological traits varied between populations and countries, though in general introduced populations, and the semi-natural population in India, showed higher performance compared to natural native populations. There was only an indication that natural enemy damage, which was significantly higher in the native range, negatively affected reproductive units. Within the introduced range, the percentage colonisation of AMF was negatively associated with plant performance indicating that I. glandulifera may associate with an incompatible AMF species incurring a cost to invasive populations. We conclude that species which are heavily regulated in the native range, though still show high levels of performance, should be considered undesirable introductions into similar ecoclimatic ranges due to the potential that these species will become highly invasive species.

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References

  • Abramoff MD, Magelhaes PJ, Ram SJ (2004) Image processing with ImageJ. Biophotonics Int 11:36–42

    Google Scholar 

  • Andrews M, Maule HG, Raven JA, Mistry A (2005) Extension growth of Impatiens glandulifera at low irradiance: importance of nitrate and potassium accumulation. Ann Bot 95:641–648

    Article  CAS  PubMed  Google Scholar 

  • Balasuriya J (1999) Shoot population density and shoot weight of clonal tea (Camellia sinensis) at different altitudes in Sri Lanka. Eur J Agron 11:123–130

    Article  Google Scholar 

  • Beerling DJ, Perrins JM (1993) Impatiens glandulifera Royle (Impatiens roylei Walp.). J Ecol 81:367–382

    Article  Google Scholar 

  • Blatter E (1927) Beautiful flowers of Kashmir. John Bale Sons and Danielsson, Ltd., London

    Google Scholar 

  • Blossey B, Nötzold R (1995) Evolution of increased competitive ability in invasive nonindigenous plants: a hypothesis. J Ecol 83:887–889

    Article  Google Scholar 

  • Caño L, Escarré J, Fleck I, Blanco-Moreno J, Sans FX (2008) Increased fitness and plasticity of an invasive species in its introduced range: A study using Senecio pterophorus. J Ecol 96:468–476

    Article  Google Scholar 

  • Cockel CP, Tanner RA (2011) Impatiens glandulifera Royle (Himalayan balsam). In: Francis RA (ed) A handbook of global freshwater invasive species. Earthscan, London, pp 67–77

    Google Scholar 

  • Crawley MJ (1987) What makes a community invisible? In: Gray AJ, Crawley MJ, Edwards PJ (eds) Colonisation succession and stability. Blackwell Scientific, Oxford, pp 429–453

    Google Scholar 

  • Ebeling SK, Hensen I, Auge H (2008) The invasive shrub Buddleja davidii performs better in its introduced range. Divers Distrib 14:225–233

    Article  Google Scholar 

  • Environment Agency (2010) Our river habitats: the state of river habitats in England, Wales and the Isles of Man: a snap shot. Environment Agency, London

    Google Scholar 

  • Erfmeier A, Bruelheide H (2004) Comparison of native and invasive Rhododendron ponticum populations: growth, reproduction and morphology under field conditions. Flora 199:120–133

    Article  Google Scholar 

  • Fowler SV, Holden ANG (1994) Classical biological control for exotic invasive weeds in riparian and aquatic habitats: practice and prospects. In: de Waal LC, Child LE, Wade PM, Brock JH (eds) Ecology and management of invasive riverside plants. Wiley, Chichester, pp 173–182

    Google Scholar 

  • Gaertner M, Breeyen A, Cang H, Richardson DM (2009) Impacts of alien plant invasions on species richness in Mediterranean-type ecosystems: a meta-analysis. Prog Phys Geogr 33:319–338

    Article  Google Scholar 

  • Harner MJ, Mummey DL, Stanford JA, Matthias CR (2010) Arbuscular mycorrhizal fungi enhance spotted knapweed growth across a riparian chronosequence. Biol Invasions 12:1481–1490

    Article  Google Scholar 

  • Harris CM, Stanford HL, Edwards C, Travis JMJ, Park KJ (2011) Integrating demographic data and a mechanistic dispersal model to predict invasion spread of Rhododendron ponticum in different habitats. Ecol Inform 6:187–195

    Article  Google Scholar 

  • Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:283–335

    Article  Google Scholar 

  • Hierro JL, Maron JL, Callaway RM (2005) A biogeographical approach to plant invasions: the importance of studying exotics in their introduced and native range. J Ecol 93:5–15

    Article  Google Scholar 

  • Hulme PE, Bremner ET (2006) Assessing the impact of Impatiens glandulifera on riparian habitats: partitioning diversity components following species removal. J Appl Ecol 43:43–50

    Article  Google Scholar 

  • Jakobs G, Weber E, Edwards PJ (2004) Introduced plants of the invasive Solidago gigantea (asteraceae) are larger and grow denser than conspecifics in the native range. Divers Distrib 10:11–19

    Article  Google Scholar 

  • Keane RM, Crawley MJ (2002) Exotic plant invasions and the enemy release hypothesis. Trends Ecol Evol 17:164–170

    Article  Google Scholar 

  • Kleunen M, Schlaepfer DR, Glaettli M, Fischer M (2011) Preadapted for invasiveness: do species traits or their plastic response to shading differ between invasive and non-invasive plant species in their native range? J Biogeogr 38:1294–1304

    Article  Google Scholar 

  • Klironomos JN (2002) Feedback with soil biota contributes to plant rarity and invasiveness in communities. Nature 417:67–70

    Article  CAS  PubMed  Google Scholar 

  • Kofidis G, Bosabalidis AM, Moustakas M (2007) Combined effects of altitude and season on leaf characteristics of Clinopodium vulgare L. (Labiatae). Environ Exp Bot 60:69–76

    Article  Google Scholar 

  • Krebs C, Gerber E, Matthies D, Schaffner U (2011) Herbivore resistance of invasive Fallopia species and their hybrids. Oecologia. doi:10.1007/s00442-011-2035-8

    Google Scholar 

  • Levine JM, Pachepsky E, Kendall BE, Yelenik SG, Lambers JH (2006) Plant–soil feedbacks and invasive spread. Ecol Lett 9:1005–1014

    Article  PubMed  Google Scholar 

  • Liu H, Stiling P (2006) Testing the enemy release hypothesis: a review and meta-analysis. Biol Invasions 8:1535–1545

    Article  Google Scholar 

  • McGonigle TP, Miller MH, Evans DG, Fairchild GL, Swan JA (1990) A new method which gives an objective measure of colonization of roots by vesicular–arbuscular mycorrhizal fungi. New Phytol 115:495–501

    Article  Google Scholar 

  • Olckers T, Hulley PE (1991) Impoverished insect herbivore faunas on the exotic bugweed Solanum mauritianum Scop. relative to indigenous Solanum species in Natal/KwaZulu and the Transkei. J Entomol Soc 54:39–50

    Google Scholar 

  • Pan H, Liu X, Cai X, Du Z, He F, Wang L, Jia C, Li M (2009) Growth and morphological responses of Fargesia angustissima to altitude in the Wolong nature reserve, southwestern China. Acta Ecol Sin 29:144–149

    Article  Google Scholar 

  • Pimentel D, McNair S, Janecka J, Wightman J, Simmonds C, O’Connell C, Wong E, Russel L, Zern J, Aquino T, Tsomondo T (2001) Economic and environmental threats of alien plant, animal, and microbe invasions. Agric Ecosyst Environ 84:1–20

    Article  Google Scholar 

  • Pimentel D, Zuniga R, Morrison D (2005) Update on the environmental and economic costs associated with alien-invasive species in the United States. Ecol Econ 52:273–288

    Article  Google Scholar 

  • Piskorz R, Klimko M (2006) The effect of Puccinia komarovii Tranzsch. infection on characters of Impatiens parviflora DC. in Galio silvatici-Carpinetum (R. Tx. 1937) Oberd. 1957 forest association. Acta Soc Bot Pol 75:51–59

    Article  Google Scholar 

  • Polunin O, Stainton A (1997) Concise flowers of the Himalaya. Oxford University Press, Oxford

    Google Scholar 

  • Prati D, Bossdorf O (2004) Allelopathic inhibition of germination by Alliaria petiolata (Brassicaceae). Am J Bot 91:285–288

    Article  PubMed  Google Scholar 

  • Pyšek P, Prach K (1995) Invasion dynamics of Impatiens glandulifera: a century of spreading reconstructed. Biol Conserv 74:41–48

    Article  Google Scholar 

  • R Development Core Team (2011) R: a language and environment for statistical computing. R foundation for statistical computing,Vienna, Austria. ISBN: 3-900051-07-01

  • Richards CL, Bossdorf O, Muth NZ, Gurevitch J, Pigliucci M (2006) Jack of all trades, master of some? On the role of phenotypic plasticity in plant invasions. Ecol Lett 9:981–993

    Article  PubMed  Google Scholar 

  • Sanders IR (2002) Specificity in the arbuscular mycorrhizal symbiosis. In: van der Heijden MGA, Sanders IR (eds) Mycorrhizal ecology. Springer, Verlag, pp 415–437

    Chapter  Google Scholar 

  • Seifert EK, Bever JD, Maron JL (2009) Evidence for the evolution of reduced mycorrhizal dependence during plant invasion. Ecology 90:1055–1062

    Article  PubMed  Google Scholar 

  • Sharma BM, Jamwal PS (1988) Flora of upper liddar valleys of Kashmir Himalaya. Scientific Publishers, Jodhpur

    Google Scholar 

  • Skálová H, Havíčková V, Pyšek P (2012) Seedling traits, plasticity and local differentiation as strategies of invasive species of Impatiens in central Europe. Ann Bot 110:1429–1438

    Article  PubMed Central  PubMed  Google Scholar 

  • St. Quinton JM, Fay MF, Ingrouille M, Faull J (2011) Characterisation of Rubus niveus: a prerequisite to its biological control in oceanic islands. Biocontrol Sci Technol 21:733–752

    Article  Google Scholar 

  • Tanner RA (2012) An ecological assessment of Impatiens glandulifera in its introduced and native range and the potential for its classical biological control. Dissertation, Royal Holloway, University of London

  • Tanner R, Ellison C, Shaw R, Evans H, Gange A (2008) Losing patience with Impatiens: are natural enemies the solution? Outlook Pest Manag 19:86–91

    Article  Google Scholar 

  • Tanner RA, Varia S, Eschen E, Wood S, Murphy ST, Gange AC (2013) Impacts of an invasive non-native annual weed, Impatiens glandulifera, on above- and below-ground invertebrate communities in the United Kingdom. PLoS ONE 8(6):e67271. doi:10.1371/journal.pone.0067271

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Vierheilig H, Coughlan AP, Wyss U, Piché Y (1998) Ink and vinegar, a simple staining technique for arbuscular-mycorrhizal fungi. Appl Environ Microbiol 64:5004–5007

    CAS  PubMed Central  PubMed  Google Scholar 

  • Vilà M, Basnou C, Pyšek P, Josefsson M, Genovesi P, Gollasch S et al (2010) How well do we understand the impacts of alien species on ecosystem services? A pan-European, cross-taxa assessment. Front Ecol Environ 8:135–144

    Article  Google Scholar 

  • Vogelsang KM, Reynolds HL, Bever JD (2006) Mycorrhizal fungal identity and richness determine the diversity and productivity of a tallgrass prairie system. New Phytol 172:554–562

    Article  PubMed  Google Scholar 

  • Widmer TL, Guermache F, Dolgovskaia MY, Reznik SY (2007) Enhanced growth and seed properties in introduced vs. native populations of yellow starthistle (Centaurea solstitialis). Weed Sci 55:465–473

    Article  CAS  Google Scholar 

  • Williams F, Eschen R, Harris A, Djeddour D, Pratt C, Shaw RS, Varia S, Lamontagne-Godwin J, Thomas SE, Murphy ST (2010) The economic cost of invasive non-native species to the British economy. CABI, Wallingford, UK

  • Williamson M (1996) Biological invasions. Chapman and Hall, London

    Google Scholar 

  • Zou J, Rogers WE, Sieman E (2007) Differences in morphological and physiological traits between native and invasive populations of Sapium sebiferum. Funct Ecol 21:721–730

    Article  Google Scholar 

  • Zuppinger-Dingley D, Schmid B, Chen Y, Brandl H, Heijden MGA, Joshi J (2011) In their native range, invasive plants are held in check by negative soil-feedbacks. Ecosphere 2:1–12

    Google Scholar 

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Acknowledgments

This work was supported by the UK Department for Environment, Food and Rural Affairs (DEFRA) and the Scottish Executive. We would like to thank all landowners for allowing access to their land for this study. We would also like to thank Sonal Varia, Corin Pratt and Mool Chand Singh for providing field support.

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Correspondence to Robert A. Tanner.

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Communicated by Lara Souza.

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Tanner, R.A., Jin, L., Shaw, R. et al. An ecological comparison of Impatiens glandulifera Royle in the native and introduced range. Plant Ecol 215, 833–843 (2014). https://doi.org/10.1007/s11258-014-0335-x

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