Skip to main content

Hybridization-prone plant families do not generate more invasive species

Abstract

Many plant taxa are both hybrid-derived and invasive, suggesting a causal connection. However, given that hybridization is not rare in plants, we should expect some fraction of invasive taxa to be hybrids, even in the absence of an underlying causal relationship. Here, we test the hypothesis that hybridization leads to invasiveness by asking whether the number of hybrids and the numbers of naturalized, weedy, and invasive taxa are correlated across 256 vascular plant families. Data were derived from six regional floras and three global databases listing weeds and invasives. To account for phylogenetic nonindependence, we combined a supertree analysis with phylogenetically independent contrasts. After correcting for family size and phylogeny, we conclude that vascular plant families with a higher propensity for hybridization are not more likely to produce more naturalized, weedy, or invasive species than families less prone to hybridization. Instead, hybridization-prone families were in some cases associated with fewer naturalized species and invaders. We present two hypotheses for these patterns, one based on Levin’s (Syst Bot 31:8–12, 2006) ideas on reproductive interference and another based on Darwin’s naturalization hypothesis. While these results do not preclude the possibility that hybridization generates weedy and invasive taxa with some frequency, they do suggest that the signal from the hybridization-invasion process may be relatively weak and easily obscured by other processes governing plant invasions.

This is a preview of subscription content, access via your institution.

Fig. 1
Fig. 2
Fig 3

References

  • Anderson E (1949) Introgressive hybridization. Chapman & Hall, London

    Google Scholar 

  • Anderson E, Stebbins GL (1954) Hybridization as an evolutionary stimulus. Evolution 8:378–388

    Article  Google Scholar 

  • Arnold ML (1997) Natural hybridization and evolution. Oxford University Press, Oxford

    Google Scholar 

  • Baker HG (1986) Patterns of plant invasion in North America. In: Mooney HA, Drake JA (eds) Ecology of biological invasions in North America and Hawaii. Springer, New York, pp 44–57

    Google Scholar 

  • Cadotte MW, Murray BR, Lovett-Doust J (2006) Evolutionary and ecological influences of plant invader success in the flora of Ontario. Ecoscience 13:388–395

    Article  Google Scholar 

  • Campbell LG, Snow AA, Ridley CE (2006) Weed evolution after crop gene introgression: greater survival and fecundity of hybrids in a new environment. Ecol Lett 9:1198–1209

    Article  PubMed  Google Scholar 

  • Cronquist A, Holmgren SH, Holmgren NH, Reveal JL, Holmgren PK (1972–2005) Intermountain flora, vols 1, 2B, 3A, 3B, 4, 5, 6. Hafner, New York

    Google Scholar 

  • Daehler CC (1998) The taxonomic distribution of invasive angiosperm plants: ecological insights and comparison to agricultural weeds. Biol Conserv 84:167–180

    Article  Google Scholar 

  • Darwin C (1859) On the origin of species by means of natural selection, or the preservation of favoured races in the struggle for life. John Murray, London

    Google Scholar 

  • Davies TJ, Barraclough TG, Chase MW, Soltis PS, Soltis DE, Savolainen V (2004) Darwin’s abominable mystery: insights from a supertree of the angiosperms. Proc Natl Acad Sci USA 101:1904–1909

    Article  PubMed  CAS  Google Scholar 

  • Ellstrand NC, Schierenbeck KA (2000) Hybridization as a stimulus for the evolution of invasiveness in plants? Proc Natl Acad Sci USA 97:7043–7050

    Article  PubMed  CAS  Google Scholar 

  • Ellstrand NC, Whitkus R, Rieseberg LH (1996) Distribution of spontaneous plant hybrids. Proc Natl Acad Sci USA 93:5090–5093

    Article  PubMed  CAS  Google Scholar 

  • Façon B, Jarne P, Pointier JP, David P (2005) Hybridization and invasiveness in the freshwater snail Melanoides tuberculata: hybrid vigour is more important than increase in genetic variance. J Evol Biol 18:524–535

    Article  PubMed  Google Scholar 

  • Felsenstein J (1985) Phylogenies and the comparative method. Am Nat 125:1–15

    Article  Google Scholar 

  • Garland T, Dickerman AW, Janis CM, Jones JA (1993) Phylogenetic analysis of covariance by computer simulation. Syst Biol 42:265–292

    Google Scholar 

  • Garland T, Midford PE, Ives AR (1999) An introduction to phylogenetically based statistical methods, with a new method for confidence intervals on ancestral values. Am Zool 39:374–388

    Google Scholar 

  • Great Plains Flora Association (1986) Flora of the Great Plains. University Press of Kansas, Lawrence

    Google Scholar 

  • Greenwood H, O’Dowd DJ, Lake PS (2004) Willow (Salix × rubens) invasion of the riparian zone in south-eastern Australia: reduced abundance and altered composition of terrestrial arthropods. Divers Distrib 10:485–492

    Article  Google Scholar 

  • Guo QF, Qian H, Ricklefs RE, Xi WM (2006) Distributions of exotic plants in eastern Asia and North America. Ecol Lett 9:827–834

    Article  PubMed  Google Scholar 

  • Hickman JC (1993) The Jepson manual: higher plants of California. University of California Press, Berkeley

    Google Scholar 

  • ISSG (2007) Global invasive species database. Invasive Species Specialist Group, IUCN Species Survival Commission, Auckland. http://www.issg.org/database.. Accessed 2 July 2007

  • Levin DA (2006) The spatial sorting of ecological species: ghost of competition or of hybridization past? Syst Bot 31:8–12

    Article  Google Scholar 

  • Levin DA, FranciscoOrtega J, Jansen RK (1996) Hybridization and the extinction of rare plant species. Conserv Biol 10:10–16

    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 

  • Maddison WP, Maddison DR (2006) Mesquite: a modular system for evolutionary analysis. http://mesquiteproject.org

  • Magee DW, Ahles HE (1999) Flora of the Northeast: a manual of the vascular flora of New England and adjacent New York. University of Massachusetts Press, Amherst

    Google Scholar 

  • Martins EP, Garland T (1991) Phylogenetic analyses of the correlated evolution of continuous characters—a simulation study. Evolution 45:534–557

    Article  Google Scholar 

  • Midford PE, Garland T Jr, Maddison W (2002) PDAP:PDTREE package for Mesquite, version 1.00. http://mesquiteproject.org/pdap_mesquite/

  • Palmer DD (2003) Hawai’i’s ferns and fern allies. University of Hawai’i Press, Honolulu

    Google Scholar 

  • Pilson D, Prendeville HR (2004) Ecological effects of transgenic crops and the escape of transgenes into wild populations. Annu Rev Ecol Evol Syst 35:149–174

    Article  Google Scholar 

  • Pyšek P (1998) Is there a taxonomic pattern to plant invasions? Oikos 82:282–294

    Article  Google Scholar 

  • Randall RP (2002) A global compendium of weeds. R.G. and F.J. Richardson, Meredith

    Google Scholar 

  • Randall RP (2007) Plant database. Western Australian Department of Agriculture and Food. Unpublished data

  • Rattenbury JA (1962) Cyclic hybridization as a survival mechanism in New Zealand forest flora. Evolution 16:348–363

    Article  Google Scholar 

  • Rejmánek M, Randall JM (2004) The total number of naturalized species can be a reliable predictor of the number of alien pest species. Divers Distrib 10:367–369

    Article  Google Scholar 

  • Rejmánek M, Richardson DM, Higgins SI, Pitcairn MJ, Grotkopp E (2005) Ecology of invasive plants: state of the art. In: Mooney HA, Mack RN, McNeely JA, Neville LE, Schei PJ, Waage JK (eds) Invasive alien species: a new synthesis. Island Press, Washington, pp 104–161

    Google Scholar 

  • Richardson DM, Pyšek P, Rejmánek M, Barbour MG, Panetta FD, West CJ (2000) Naturalization and invasion of alien plants: concepts and definitions. Divers Distrib 6:93–107

    Article  Google Scholar 

  • Rieseberg LH, Raymond O, Rosenthal DM, Lai Z, Livingstone K, Nakazato T, Durphy JL, Schwarzbach AE, Donovan LA, Lexer C (2003) Major ecological transitions in wild sunflowers facilitated by hybridization. Science 301:1211–1216

    Article  PubMed  CAS  Google Scholar 

  • Rieseberg LH, Kim SC, Randell RA, Whitney KD, Gross BR, Lexer C, Clay K (2007) Hybridization and the colonization of novel habitats by annual sunflowers. Genetica 129:149–165

    Article  PubMed  Google Scholar 

  • SAS Institute (2003) The SAS system for windows, release 9.1. SAS Institute, Cary

    Google Scholar 

  • Smith AR, Pryer KM, Schuettpelz E, Korall P, Schneider H, Wolf PC (2006) A classification for extant ferns. Taxon 55:705–731

    Google Scholar 

  • Stace CE (1975) Hybridization and the flora of the British Isles. Academic Press, London

    Google Scholar 

  • Stace CA (1997) New flora of the British Isles, 2nd edn. Cambridge University Press, Cambridge

    Google Scholar 

  • Stebbins GL (1959) The role of hybridization in evolution. Proc Am Philos Soc 103:231–251

    Google Scholar 

  • Stebbins GL (1969) The significance of hybridization for plant taxonomy and evolution. Taxon 18:26–35

    Google Scholar 

  • Stebbins GL (1985) Polyploidy, hybridization, and the invasion of new habitats. Ann Mo Bot Gard 72:824–832

    Article  Google Scholar 

  • Stevens JE (2006) Angiosperm phylogeny website, version 7, May 2006. http://www.mobot.org/MOBOT/research/APweb/

  • Strauss SY, Webb CO, Salamin N (2006) Exotic taxa less related to native species are more invasive. Proc Natl Acad Sci USA 103:5841–5845

    Article  PubMed  CAS  Google Scholar 

  • Vilà M, Weber E, D’Antonio CM (2000) Conservation implications of invasion by plant hybridization. Biol Invasions 2:207–217

    Article  Google Scholar 

  • Wagner WL, Herbst DR, Somer SH (1999) Manual of the flowering plants of Hawai’i. University of Hawai’i Press, Honolulu

    Google Scholar 

  • Webb CO, Donoghue MJ (2005) Phylomatic: tree assembly for applied phylogenetics. Mol Ecol Notes 5:181–183

    Article  Google Scholar 

  • Webb CO, Ackerly DD, McPeek MA, Donoghue MJ (2002) Phylogenies and community ecology. Annu Rev Ecol Syst 33:475–505

    Article  Google Scholar 

  • Weber E (2003) Invasive plant species of the world: a reference guide to environmental weeds. CABI Publishing, Wallingford

    Google Scholar 

  • Whitney KD, Randell RA, Rieseberg LH (2006) Adaptive introgression of herbivore resistance traits in the weedy sunflower Helianthus annuus. Am Nat 167:794–807

    Article  Google Scholar 

Download references

Acknowledgements

We thank Kristina Schierenbeck and Debra Ayres for organizing the Botanical Society of America symposium that sparked this analysis. Norm Ellstrand, Loren Rieseberg, and Richard Whitkus kindly shared their data and methods. Many thanks to Peter Stevens for maintaining the Angiosperm Phylogeny Website and for advice on placement of genera, to Rod Randall for sharing the most current version of his weeds database, and to Luke Harmon for advice on phylogenetic correction. Prudence Sun, John Land, and Kate Boles provided assistance with data entry. Discussions with Loren Rieseberg and Jennifer Rudgers greatly improved the manuscript. This work was funded in part by a Wray-Todd Fellowship to J.R.A. and NSF DEB 0716868 to K.D.W.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kenneth D. Whitney.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Whitney, K.D., Ahern, J.R. & Campbell, L.G. Hybridization-prone plant families do not generate more invasive species. Biol Invasions 11, 1205–1215 (2009). https://doi.org/10.1007/s10530-008-9390-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10530-008-9390-3

Keywords

  • Adaptation
  • Evolution of invasiveness
  • Introgression
  • Phylogenetically independent contrasts
  • Vascular plant hybrids
  • Weeds