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19 - Effects of natural enemies on tropical woody-plant invasions

Published online by Cambridge University Press:  25 August 2009

Saara J. Dewalt
Affiliation:
Rice University
David Burslem
Affiliation:
University of Aberdeen
Michelle Pinard
Affiliation:
University of Aberdeen
Sue Hartley
Affiliation:
University of Sussex
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Summary

Plant invasions pose a current and increasing threat to species diversity and composition of forests worldwide. Biological invasions are natural ecological processes and the movement of plants across geographic barriers has always occurred (Sauer 1988), but humans have greatly accelerated the rate of introductions and moved plants across barriers that probably would not have been spanned naturally. Many of these plant introductions, whether deliberate or accidental, have had negative effects in the areas of introduction. Plant invasions have led to native species loss, altered ecosystem-level processes and caused enormous economic and environmental damage in various ecosystems, including tropical forests (Vitousek et al. 1987; Gordon 1998; Parker et al. 1999; Mack et al. 2000). Remote tropical islands and fragmented landscapes are particularly vulnerable to invasion by non-native plants (Laurance et al. 2002; Denslow 2003), but continental species-rich tropical rainforests also are invasible (Usher 1991; Rejmánek 1996a), particularly following natural or human disturbance (Whitmore 1991). Because of such negative impacts, species invasions are seen as one of the primary agents of global change (Vitousek et al. 1996), and tropical forests are unlikely to be immune (Fine 2002).

This chapter explores how biotic interactions, particularly herbivory and pathogen attack, may affect the abundance and distribution of invasive woody species in tropical rainforests. Specifically, I examine whether herbivores and fungal pathogens (natural enemies) are important determinants of species' abundance and distribution in their native ranges and whether the absence or reduced impact of these natural enemies may explain why certain introduced woody plants are successful invaders in tropical rainforests.

Type
Chapter
Information
Biotic Interactions in the Tropics
Their Role in the Maintenance of Species Diversity
, pp. 459 - 483
Publisher: Cambridge University Press
Print publication year: 2005

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References

Agrawal, A. A. & Kotanen, P. M. (2003) Herbivores and the success of exotic plants: a phylogenetically controlled experiment. Ecology Letters, 6, 712–715CrossRefGoogle Scholar
Alvarez-Buylla, E. R. (1994) Density dependence and patch dynamics in tropical rain forests: matrix models and applications to a tree species. American Naturalist, 143, 155–191CrossRefGoogle Scholar
Amsellem, L., Noyer, J. L., Bourgeois, T. & Hossaert-McKey, M. (2000) Comparison of genetic diversity of the invasive weed Rubus alceifolius Poir. (Rosaceae) in its native range and in areas of introduction, using amplified fragment length polymorphism (AFLP) markers. Molecular Ecology, 9, 443–455CrossRefGoogle ScholarPubMed
Augspurger, C. K. (1983) Seed dispersal of the tropical tree Platypodium elegans and the escape of its seedlings from fungal pathogens. Journal of Ecology, 71, 759–772CrossRefGoogle Scholar
Augspurger, C. K. (1984) Seedling survival of tropical tree species: interactions of dispersal distance, light-gaps, and pathogens. Ecology, 65, 1705–1712CrossRefGoogle Scholar
Augspurger, C. K. & Kelly, C. K. (1984) Pathogen mortality of tropical tree seedlings: experimental studies of effects of dispersal distance, seedling density, and light conditions. Oecologia, 61, 211–217CrossRefGoogle ScholarPubMed
Baruch, Z., Pattison, R. R. & Goldstein, G. (2000) Responses to light and water availability of four invasive Melastomataceae in the Hawaiian Islands. International Journal of Plant Sciences, 161, 107–118CrossRefGoogle ScholarPubMed
Beckstead, J. & Parker, I. M. (2003) Invasiveness of Ammophila arenaria: release from soil-borne pathogens?Ecology, 84, 2824–2831CrossRefGoogle Scholar
Binggeli, P., Hall, J. B. & Healey, J. R. (1998) A review of invasive woody plants in the tropics. School of Agricultural and Forest Sciences Publication Number 13. Bangor: University of WalesGoogle Scholar
Blaney, C. S. & Kotanen, P. M. (2001a) Effects of fungal pathogens on seeds of native and exotic plants: a test using congeneric pairs. Journal of Applied Ecology, 38, 1104–1113CrossRefGoogle Scholar
Blaney, C. S. & Kotanen, P. M. (2001b) Post-dispersal losses to seed predators: an experimental comparison of native and exotic old field plants. Canadian Journal of Botany, 79, 284–292CrossRefGoogle Scholar
Blossey, B. & Kamil, J. (1996) What determines the increased competitive ability of invasive non-indigenous plants? In IX International Symposium on Biological Control (ed. , V. C. Moran & , J. H. Hoffmann), Stellenbosch, South Africa: University of Cape Town, pp. 3–9Google Scholar
Blossey, B. & Nötzold, R. (1995) Evolution of increased competitive ability in invasive nonindigenous plants: a hypothesis. Journal of Ecology, 83, 887–889CrossRefGoogle Scholar
Bossard, C. C. & Rejmánek, M. (1994) Herbivory, growth, seed production, and resprouting of an exotic invasive shrub. Biological Conservation, 67, 193–200CrossRefGoogle Scholar
Buckley, Y. M., Downey, P., Fowler, S. V.et al. (2003) Are invasives bigger? A global study of seed size variation in two invasive shrubs. Ecology, 84, 1434–1440CrossRefGoogle Scholar
Carlquist, S. (1974) Island Biology. New York: Columbia University PressCrossRefGoogle Scholar
Carson, W. P. & Root, R. B. (2000) Herbivory and plant species coexistence: community regulation by an outbreaking phytophagous insect. Ecological Monographs, 70, 73–99CrossRefGoogle Scholar
Caswell, H. (2001) Matrix Population Models: Construction, Analysis, and Interpretation, 2nd edn. Sunderland, MA: SinauerGoogle Scholar
Coley, P. D. & Barone, J. A. (1996) Herbivory and plant defenses in tropical forests. Annual Review of Ecology and Systematics, 27, 305–335CrossRefGoogle Scholar
Connell, J. H. (1971) On the role of natural enemies in preventing competitive exclusion in some marine animals and in rain forest trees. In Advanced Study Institute on Dynamics of Numbers in Populations (ed. , P. J. Den Boer & , G. Gradwell). Wageningen: Centre for Agricultural Publishing and Documentation, pp. 298–312Google Scholar
Crawley, M. J. (1987) What makes a community invasible? In Colonization, Succession, and Stability (ed. , A. J. Gray, , M. J. Crawley & , P. J. Edwards). Oxford: Blackwell, pp. 429–453Google Scholar
Daehler, C. C. (2001) Darwin's naturalization hypothesis revisited. American Naturalist, 158, 324–330CrossRefGoogle ScholarPubMed
Darwin, C. (1859) The Origin of Species. Oxford: Oxford University PressGoogle Scholar
Davis, M. A., Grime, J. P. & Thompson, K. (2000) Fluctuating resources in plant communities: a general theory of invasibility. Journal of Ecology, 88, 528–534CrossRefGoogle Scholar
Kroon, H., Plaisier, A., Groenendael, J. & Caswell, H. (1986) Elasticity: the relative contributions of demographic parameters to population growth rate. Ecology, 67, 1427–1431CrossRefGoogle Scholar
Debach, P. & Rosen, D. (1991) Biological Control by Natural Enemies. Cambridge: Cambridge University PressGoogle Scholar
Denoth, M., Frid, L. & Myers, J. H. (2002) Multiple agents in biological control: improving the odds?Biological Control, 24, 20–30CrossRefGoogle Scholar
Denslow, J. S. (2003) Weeds in paradise: thoughts on the invasibility of tropical islands. Annals of the Missouri Botanical Garden, 90, 119–127CrossRefGoogle Scholar
DeWalt, S. J. (2003) The invasive tropical shrub Clidemia hirta (Melastomataceae) in its native and introduced ranges: tests of hypotheses of invasion. Unpublished Ph.D. dissertation, Louisiana State University
DeWalt, S. J., Denslow, J. S. & Hamrick, J. L. (2004a) Biomass allocation, growth, and photosynthesis of genotypes from the native and introduced ranges of the tropical shrub Clidemia hirta. Oecologia, 138, 521–531CrossRefGoogle Scholar
DeWalt, S. J., Denslow, J. S. & Ickes, K. (2004b) Natural-enemy release facilitates habitat expansion of the invasive tropical shrub Clidemia hirta. Ecology, 85, 471–483CrossRefGoogle Scholar
DeWalt, S. J. & Hamrick, J. L. (2004) Genetic variation of introduced Hawaiian and native Costa Rican populations of an invasive tropical shrub, Clidemia hirta (Melastomataceae). American Journal of Botany, 91, 1155–1163CrossRefGoogle Scholar
Duncan, R. P. & Williams, P. A. (2002) Darwin's naturalization hypothesis challenged. Nature, 417, 608–609CrossRefGoogle ScholarPubMed
Elton, C. S. (1958) The Ecology of Invasions of Animals and Plants. London: MethuenCrossRefGoogle Scholar
Fenner, M. & Lee, W. G. (2001) Lack of pre-dispersal seed predators in introduced Asteraceae in New Zealand. New Zealand Journal of Ecology, 25, 95–99Google Scholar
Fine, P. V. A. (2002) The invasibility of tropical forests by exotic plants. Journal of Tropical Ecology, 18, 687–705CrossRefGoogle Scholar
Fowler, S. V., Harman, H. M., Memmott, J. et al. (1996) Comparing the population dynamics of broom, Cytisus scoparius, as a native plant in the United Kingdom and France and as an invasive alien weed in Australia and New Zealand. In IX International Symposium on Biological Control (ed. , V. C. Moran & , J. H. Hoffmann) Stellenbosch: University of Cape Town, pp. 19–26Google Scholar
Fryer, G. (1991) Biological invasions into tropical nature reserves. In Ecology of Biological Invasions in the Tropics (ed. , P. S. Ramakrishnan). New Delhi: International Scientific Publications, pp. 87–101Google Scholar
Gagné, B. H., Loope, L. L., Medeiros, A. C. & Anderson, S. J. (1992) Miconia calvescens: a threat to native forests of the Hawaiian Islands. Pacific Science, 46, 390–391Google Scholar
Gaskin, J. F. & Schaal, B. A. (2002) Hybrid Tamarix widespread in US invasion and undetected in native Asian range. Proceedings of the National Academy of Sciences, 99, 11256–11259CrossRefGoogle Scholar
Gilbert, G. S. & DeSteven, D. (1996) A canker disease of seedlings and saplings of Tetragastris panamensis (Burseraceae) caused by Botryosphaeria dothidea in a lowland tropical forest. Plant Disease, 80, 684–687CrossRefGoogle Scholar
Gordon, D. (1998) Effects of invasive, non-indigenous plant species on ecosystem processes: lessons from Florida. Ecological Applications, 8, 975–989CrossRefGoogle Scholar
Hammond, D. S. & Brown, V. K. (1998) Disturbance, phenology and life-history characteristics: factors influencing distance/density-dependent attack on tropical seeds and seedlings. In Dynamics of Tropical Communities (ed. , D. M. Newbery, , H. H. T. Prins & , N. D. Brown). Oxford: Blackwell, pp. 51–78Google Scholar
Harper, J. L. (1969) The role of predation in vegetational diversity. Brookhaven Symposia in Biology, 22, 48–62Google ScholarPubMed
Herbold, B. & Moyle, P. B. (1986) Introduced species and vacant niches. American Naturalist, 128, 751–760CrossRefGoogle Scholar
HilleRisLambers, J., Clark, J. S. & Beckage, B. (2002) Density-dependent mortality and the latitudinal gradient in species diversity. Nature, 417, 732–735CrossRefGoogle Scholar
Hoffmann, J. H., Impson, F. A. C. & Volchansky, C. R. (2002) Biological control of cactus weeds: implications of hybridization between control agent biotypes. Journal of Applied Ecology, 39, 900–908CrossRefGoogle Scholar
Horvitz, C. C. & Schemske, D. W. (1995) Spatiotemporal variation in demographic transitions of a tropical understorey herb: projection matrix analysis. Ecological Monographs, 65, 155–192CrossRefGoogle Scholar
Howarth, F. G. (1991) Environmental impacts of classical biological control. Annual Review of Entomology, 36, 485–509CrossRefGoogle Scholar
Huffaker, C. B. & Kennett, C. E. (1959) A ten-year study of vegetational changes associated with biological control of Klamath weed. Journal of Range Management, 12, 69–82CrossRefGoogle Scholar
Janzen, D. H. (1970) Herbivores and the number of tree species in tropical forests. American Naturalist, 104, 501–528CrossRefGoogle Scholar
Keane, R. M. & Crawley, M. J. (2002) Exotic plant invasions and the enemy release hypothesis. Trends in Ecology and Evolution, 17, 164–170CrossRefGoogle Scholar
Kitajima, K. (1994) Relative importance of photosynthetic traits and allocation patterns as correlates of seedling shade tolerance of 13 tropical trees. Oecologia, 98, 419–428CrossRefGoogle ScholarPubMed
Klironomos, J. N. (2002) Feedback with soil biota contributes to plant rarity and invasiveness in communities. Nature, 417, 67–70CrossRefGoogle ScholarPubMed
Laurance, W. F., Lovejoy, T. E., Vasconcelos, H. L.et al. (2002) Ecosystem decay of Amazonian forest fragments: a 22-year investigation. Conservation Biology, 16, 605–618CrossRefGoogle Scholar
Leger, E. A. & Rice, K. J. (2003) Invasive California poppies (Eschscholzia californica Cham.) grow larger than native individuals under reduced competition. Ecology Letters, 6, 257–264CrossRefGoogle Scholar
Levine, J. M. & d'Antonio, C. M. (1999) Elton revisited: a review of evidence linking diversity and invasibility. Oikos, 87, 15–26CrossRefGoogle Scholar
Lonsdale, W. M. (1999) Global patterns of plant invasions and the concept of invasibility. Ecology, 80, 1522–1536CrossRefGoogle Scholar
Louda, S. M., Dixon, P. M. & Huntly, N. J. (1987) Herbivory in sun versus shade at a natural meadow-woodland ecotone in the Rocky Mountains. Vegetatio, 72, 141–149Google Scholar
Louda, S. M. & Potvin, M. A. (1995) Effect of inflorescence-feeding insects in the demography and lifetime fitness of a native plant. Ecology, 76, 229–245CrossRefGoogle Scholar
Louda, S. M. & Rodman, J. E. (1996) Insect herbivory as a major factor in the shade distribution of a native crucifer (Cardamine cordifolia A. Gray, bittercress). Journal of Ecology, 84, 229–237CrossRefGoogle Scholar
Lym, R. G. & Carlson, R. B. (2002) Effect of leafy spurge (Euphorbia esula) genotype on feeding damage and reproduction of Aphthona spp.: implications for biological weed control. Biological Control, 23, 127–133CrossRefGoogle Scholar
Mack, R. N. (1996) Biotic barriers to plant naturalization. In IX International Symposium on Biological Control (ed. , V. C. Moran & , J. H. Hoffmann) Stellenbosch: University of Cape Town, pp. 39–46Google Scholar
Mack, R. N., Simberloff, D., Lonsdale, W. M., Evans, H., Clout, M. & Bazzaz, F. A. (2000) Biotic invasions: causes, epidemiology, global consequences, and control. Ecological Applications, 10, 689–710CrossRefGoogle Scholar
McEvoy, P. B. & Coombs, E. M. (1999) Biological control of plant invaders: regional patterns, field experiments, and structured population models. Ecological Applications, 9, 387–401CrossRefGoogle Scholar
McEvoy, P. B., Cox, C. & Coombs, E. (1991) Successful biological control of ragwort, Senecio jacobaea, by introduced insects in Oregon. Ecological Applications, 1, 430–442CrossRefGoogle ScholarPubMed
McFadyen, R. E. C. (1998) Biological control of weeds. Annual Review of Entomology, 43, 369–393CrossRefGoogle ScholarPubMed
McNaughton, S. J. (1983) Compensatory plant growth as a response to herbivory. Oikos, 40, 329–336CrossRefGoogle Scholar
Memmott, J., Fowler, S. V., Paynter, Q., Sheppard, A. W. & Syrett, P. (2000) The invertebrate fauna on broom, Cytisus scoparius, in two native and two exotic habitats. Acta Oecologica, 21, 213–222CrossRefGoogle Scholar
Meyer, J.-Y. (1996) Status of Miconia calvescens (Melastomataceae), a dominant invasive tree in the Society Islands (French Polynesia). Pacific Science, 50, 66–76Google Scholar
Mitchell, C. E. & Power, A. G. (2003) Release of invasive plants from fungal and viral pathogens. Nature, 421, 625–627CrossRefGoogle ScholarPubMed
Muller-Landau, H. C., Levin, S. A. & Keymer, J. E. (2003) Theoretical perspectives on evolution of long-distance dispersal and the example of specialized pests. Ecology, 84, 1957–1967CrossRefGoogle Scholar
Naeem, S., Knops, J. M. H., Tilman, D., Howe, K. M., Kennedy, T. & Gale, S. (2000) Plant diversity increases resistance to invasion in the absence of covarying extrinsic factors. Oikos, 91, 97–108CrossRefGoogle Scholar
Noble, I. R. (1989). Attributes of invaders and the invading process: terrestrial and vascular plants. In Biological Invasions: A Global Perspective (ed. , J. A. Drake, , F. DiCastri, , R. H. Groves, et al.) New York: Wiley, pp. 301–313Google Scholar
Novak, S. J. & Mack, R. N. (2001) Tracing plant introduction and spread: genetic evidence from Bromus tectorum (Cheatgrass). Bioscience, 51, 114–122CrossRefGoogle Scholar
Packer, A. & Clay, K. (2000) Soil pathogens and spatial patterns of seedling mortality in a temperate tree. Nature, 404, 278–281CrossRefGoogle Scholar
Packer, A. & Clay, K. (2003) Soil pathogens and Prunus serotina seedling and sapling growth near conspecific trees. Ecology, 84, 108–119CrossRefGoogle Scholar
Parker, I. M. (2000) Invasion dynamics of Cytisus scoparius: a matrix model approach. Ecological Applications, 10, 726–743CrossRefGoogle Scholar
Parker, I. M., Simberloff, D., Lonsdale, W. M.et al. (1999) Toward a framework for understanding the ecological effects of invaders. Biological Invasions, 1, 3–19CrossRefGoogle Scholar
Paynter, Q., Fowler, S. V., Hinz, H. L. et al. (1996) Are seed-feeding insects of use for the biological control of broom? In IX International Symposium on Biological Control (ed. , V. C. Moran & , J. H. Hoffmann) Stellenbosch: University of Cape Town, pp. 495–501Google Scholar
Pimentel, D., Lach, L., Zuniga, R. & Morrison, D. (2000) Environmental and economic costs of nonindigenous species in the United States. BioScience, 50, 53–65CrossRefGoogle Scholar
Pinard, M. (1993) Impacts of stem harvesting on populations of Iriartea deltoidea (Palmae) in an extractive reserve in Acre, Brazil. Biotropica, 25, 2–14CrossRefGoogle Scholar
Prieur-Richard, A.-H., Lavorel, S., Grigulis, K. & Dos Santos, A. (2000) Plant community diversity and invasibility by exotics: invasion of Mediterranean old fields by Conzya bonariensis and Conzya canadensis. Ecology Letters, 3, 412–422CrossRefGoogle Scholar
Prieur-Richard, A.-H., Lavorel, S., Linhart, Y. B. & Dos Santos, A. (2002) Plant diversity, herbivory and resistance of a plant community to invasion in Mediterranean annual communities. Oecologia, 130, 96–104CrossRefGoogle ScholarPubMed
Pritchard, T. (1960). Race formation in weedy species with special reference to Euphorbia cyparissias L. and Hypericum perforatum L. In The Biology of Weeds: A Symposium of the British Ecological Society, Oxford, 2–4 April 1959 (ed. , J. L. Harper). Oxford: Blackwell, pp. 61–66Google Scholar
Reimer, N. J. & Beardsley, J. W. Jr (1989) Effectiveness of Liothrips urichi (Thysanoptera: Phlaeothripidae) introduced for biological control of Clidemia hirta in Hawaii. Environmental Entomology, 18, 1141–1146CrossRefGoogle Scholar
Reinhart, K. O., Packer, A., Putten, W. H. & Clay, K. (2003) Plant-soil biota interactions and spatial distribution of black cherry in its native and invasive ranges. Ecology Letters, 6, 1046–1050CrossRefGoogle Scholar
Rejmánek, M. (1996a) Species richness and resistance to invasions. In Biodiversity and Ecosystem Processes in Tropical Forests (ed. , G. Orians, , R. Dirzo & , J. H. Cushman), Vol. 122. New York: Springer, pp. 153–172Google Scholar
Rejmánek, M. (1996b) A theory of seed plant invasiveness: the first sketch. Biological Conservation, 78, 171–181CrossRefGoogle Scholar
Rejmánek, M. (1999) Invasive plant species and invasible ecosystems. In Invasive Species and Biodiversity Management (ed. , O. T. Sandlund, , P. J. Schei & , A. Viken). Dordrecht: Kluwer, pp. 79–102Google Scholar
Richardson, D. M., Allsopp, N., d'Antonio, C. M., Milton, S. J. & Rejmánek, M. (2000) Plant invasions – the role of mutualisms. Biological Reviews, 75, 65–93CrossRefGoogle ScholarPubMed
Root, R. B. (1996) Herbivore pressure on goldenrods (Solidago altissima): its variation and cumulative effects. Ecology, 77, 1074–1087CrossRefGoogle Scholar
Sagers, C. L. & Coley, P. D. (1995) Benefits and costs of defense in a neotropical shrub. Ecology, 76, 1835–1843CrossRefGoogle Scholar
Sauer, J. D. (1988) Plant Migration: The Dynamics of Geographic Patterning in Seed Plant Species. Berkeley, CA: University of California PressGoogle Scholar
Schaal, B. A., Gaskin, J. F. & Caicedo, A. L. (2003) Phylogeography, haplotype trees, and invasive plant species. Journal of Heredity, 94, 197–204CrossRefGoogle ScholarPubMed
Schierenbeck, K. A., Mack, R. N. & Sharitz, R. R. (1994) Effects of herbivory on growth and biomass allocation in native and introduced species of Lonicera. Ecology, 75, 1661–1672CrossRefGoogle Scholar
Shea, K. & Kelly, D. (1998) Estimating biocontrol agent impact with matrix models: Carduus nutans in New Zealand. Ecological Applications, 8, 824–832CrossRefGoogle Scholar
Sheil, D., Jennings, S. & Savill, P. (2000) Long-term permanent plot observations of vegetation dynamics in Bundongo, a Ugandan rain forest. Journal of Tropical Ecology, 16, 765–800CrossRefGoogle Scholar
Siemann, E. & Rogers, W. E. (2001) Genetic differences in growth of an invasive tree species. Ecology Letters, 4, 514–518CrossRefGoogle Scholar
Siemann, E. & Rogers, W. E. (2003a) Herbivory, disease, recruitment limitation, and success of alien and native tree species. Ecology, 84, 1489–1505CrossRefGoogle Scholar
Siemann, E. & Rogers, W. E. (2003b) Increased competitive ability of an invasive tree may be limited by an invasive beetle. Ecological Applications, 13, 1503–1507CrossRefGoogle Scholar
Siemann, E. & Rogers, W. E. (2003c) Reduced resistance of invasive varieties of the alien tree Sapium sebiferum to a generalist herbivore. Oecologia, 135, 451–457CrossRefGoogle Scholar
Siemann, E., Tilman, D., Haarstad, J. & Ritchie, M. (1998) Experimental tests of the dependence of arthropod diversity on plant diversity. American Naturalist, 152, 738–750CrossRefGoogle ScholarPubMed
Simberloff, D., Brown, B. J. & Lowrie, S. (1978) Isopod and insect root borers may benefit Florida mangroves. Science, 201, 630–632CrossRefGoogle ScholarPubMed
Smith, M. D. & Knapp, A. K. (1999) Exotic plant species in a C4-dominated grassland: invasibility, disturbance, and community structure. Oecologia, 120, 605–612CrossRefGoogle Scholar
Stanosz, G. R. (1994) Benomyl and acephate applications increase survival of sugar maple seedlings during their first growing season in northern Pennsylvania. Canadian Journal of Forest Research, 24, 1107–1111CrossRefGoogle Scholar
Stohlgren, T. J., Binkley, D., Chong, G. W.et al. (1999) Exotic plant species invade hot spots of native plant diversity. Ecological Monographs, 69, 25–46CrossRefGoogle Scholar
, Symstad A. J. (2000) A test of the effects of functional group richness and composition on grassland invasibility. Ecology 81, 99–109CrossRefGoogle Scholar
Tilman, D. (1997) Community invasibility, recruitment limitation, and grassland biodiversity. Ecology, 78, 81–92CrossRefGoogle Scholar
Torchin, M. E., Lafferty, K. D., Dobson, A. P., McKenzie, V. J. & Kuris, A. M. (2003) Introduced species and their missing parasites. Nature, 412, 628–630CrossRefGoogle Scholar
Usher, M. B. (1991) Biological invasions into tropical nature reserves. In Ecology of Biological Invasions in the Tropics (ed. , P. S. Ramakrishnan). New Delhi: International Scientific Publications, pp. 21–34Google Scholar
Putten, W. H. & Peters, B. A. M. (1997) How soil-borne pathogens may affect plant competition. Ecology, 78, 1785–1795CrossRefGoogle Scholar
Kleunen, M. & Schmid, B. (2003) No evidence for an evolutionary increased competitive ability in an invasive plant. Ecology, 84, 2816–2823CrossRefGoogle Scholar
Vilà, M., Gómez, A. & Maron, J. L. (2003) Are alien plants more competitive than their native conspecifics? A test using Hypericum perforatum L. Oecologia, 137, 211–215CrossRefGoogle ScholarPubMed
Vitousek, P. M., D'Antonio, C. M., Loope, L. L. & Westbrooks, R. (1996) Biological invasions as global environmental change. American Scientist, 84, 468–478Google Scholar
Vitousek, P. M., Walker, L. R., Whiteaker, L. D., Mueller-Dombois, D. & Matson, P. A. (1987) Biological invasion by Myrica faya alters ecosystem development in Hawaii. Science, 238, 802–804CrossRefGoogle ScholarPubMed
Waloff, N. & Richards, O. W. (1977) The effect of insect fauna on growth, mortality and natality of broom, Sarothamnus scoparius. Journal of Applied Ecology, 14, 787–798CrossRefGoogle Scholar
Wester, L. L. & Wood, H. B. (1977) Koster's curse (Clidemia hirta), a weed pest in Hawaiian forests. Environmental Conservation, 4, 35–41CrossRefGoogle Scholar
Whitham, T. G., Maschinski, J., Larson, K. C. & Paige, K. N. (1991) Plant responses to herbivory: the continuum from negative to positive and underlying physiological mechanisms. In Plant–Animal Interactions: Evolutionary Ecology in Tropical and Temperate Regions (ed. , P. W. Price, , T. M. Lewinsohn, , G. W. Fernandes & , W. W. Benson). New York, NY: Wiley, pp. 227–256Google Scholar
Whitmore, T. C. (1991) Invasive woody plants in perhumid tropical climates. In Ecology of Biological Invasions in the Tropics (ed. , P. S. Ramakrishnan). New Delhi: International Scientific Publications, pp. 35–40Google Scholar
Williamson, M. & Fitter, A. (1996) The characters of successful invaders. Biological Conservation, 78, 163–170CrossRefGoogle Scholar
Willis, A. J., Memmott, J. & Forrester, R. I. (2000) Is there evidence for the post-invasion evolution of increased size among invasive plant species?Ecology Letters, 3, 275–283CrossRefGoogle Scholar
Wolfe, L. M. (2002) Why alien invaders succeed: support for the escape-from-enemy hypothesis. American Naturalist, 160, 705–711Google ScholarPubMed
Zimmermann, H. G. & Moran, V. C. (1982) Ecology and management of cactus weeds in South Africa. South African Journal of Science, 78, 314–320Google Scholar

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