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Chapter Eleven - Perspective

trait-mediated indirect interactions and the coevolutionary process

Published online by Cambridge University Press:  05 February 2013

Benjamin J. Ridenhour
Affiliation:
Department of Biological Sciences, University of Notre Dame
Scott L. Nuismer
Affiliation:
Department of Biological Sciences, University of Idaho
Takayuki Ohgushi
Affiliation:
Kyoto University, Japan
Oswald Schmitz
Affiliation:
Yale University, Connecticut
Robert D. Holt
Affiliation:
University of Florida
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Summary

Multispecific coevolution and the origins of coevolutionary trait-mediated indirect interactions

The notion of coevolution between interacting species can be traced at least as far back as Darwin’s writings in the Origin of Species, where he outlines a process of coadaptation between a plant and its pollinator (Darwin 1859). Although Darwin’s description of plant–pollinator coadaptation suggests a coevolutionary process, it was not until Ehrlich and Raven’s (1964) study of butterfly and plant adaptive radiation that the term ‘coevolution’ was coined. Ehrlich and Raven used the term to signify the broad concept of any evolution resulting from biotic interactions. This broad definition of coevolution persisted until 1980.

Under the broad definition put forth by Ehrlich and Raven, it is clear that trait-mediated indirect interactions (TMIIs) are part of coevolutionary thinking. TMIIs occur when a third species affects the traits involved at the phenotypic interface of an interaction between two species (Wootton 1993; Abrams 1995; Brodie 2003); this is the definition we will use throughout this chapter for TMII. Thus, using Ehrlich and Raven’s original interpretation of coevolution, TMIIs are a subset of coevolutionary interactions (assuming actual evolutionary change in trait values is occurring). TMIIs are often distinguished from density-mediated indirect interactions (DMIIs) where the third species alters the density of a species involved in another interaction and thereby alters the outcome of that interaction.

Type
Chapter
Information
Trait-Mediated Indirect Interactions
Ecological and Evolutionary Perspectives
, pp. 207 - 220
Publisher: Cambridge University Press
Print publication year: 2012

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References

Abrams, P. A 1995 Implications of dynamically variable traits for identifying, classifying, and measuring direct and indirect effects in ecological communitiesAmerican Naturalist 146 112CrossRefGoogle Scholar
Benkman, C. W. 1999 The selection mosaic and diversifying coevolution between crossbills and lodgepole pineAmerican Naturalist 153 S75CrossRefGoogle ScholarPubMed
Benkman, C. W.Holimon, W. C.Smith, J. W. 2001 The influence of a competitor on the geographic mosaic of coevolution between crossbills and lodgepole pineEvolution 55 282CrossRefGoogle ScholarPubMed
Benkman, C. W.Parchman, T. L.Favis, A.Siepielski, A. M. 2003 Reciprocal selection causes a coevolutionary arms race between crossbills and lodgepole pineAmerican Naturalist 162 182CrossRefGoogle ScholarPubMed
Berenbaum, M. R. 1998 Chemical phenotype matching between a plant and its insect herbivoreProceedings of the National Academy of Sciences of the United States of America 95 13743CrossRefGoogle ScholarPubMed
Berenbaum, M. R.Zangerl, A. R. 2006 Parsnip webworms and host plants at home and abroad: trophic complexity in a geographic mosaicEcology 87 3070CrossRefGoogle Scholar
Brodie, E. D.Ridenhour, B. J. 2003 Reciprocal selection at the phenotypic interface of coevolutionIntegrative and Comparative Biology 43 408CrossRefGoogle ScholarPubMed
Bronstein, J. L. 1994 Conditional outcomes in mutualistic interactionsTrends in Ecology and Evolution 9 214CrossRefGoogle ScholarPubMed
Cushman, J. H.Whitham, T. G. 1989 Conditional mutualism in a membracid–ant association: temporal, age-specific, and density-dependent effectsEcology 70 1040CrossRefGoogle Scholar
Darwin, C. 1859 On the Origin of Species by Means of Natural SelectionLondonJ. MurrayGoogle Scholar
Ehrlich, P. R.Raven, P. H. 1964 Butterflies and plants: a study in coevolutionEvolution 18 586CrossRefGoogle Scholar
Fritz, R. S. 1995 Direct and indirect effects of plant genetic variation on enemy impactEcological Entomology 20 18CrossRefGoogle Scholar
Futuyma, D. J.Slatkin, M. 1983 CoevolutionSunderland, MA:Sinauer AssociatesGoogle Scholar
Gandon, S.Nuismer, S. L. 2009 Interactions between genetic drift, gene flow, and selection mosaics drive parasite local adaptationAmerican Naturalist 173 212CrossRefGoogle ScholarPubMed
Gomulkiewicz, R.Drown, D. M.Dybdahl, M. F. 2007 Dos and don’ts of testing the geographic mosaic theory of coevolutionHeredity 98 249CrossRefGoogle ScholarPubMed
Gomulkiewicz, R.Nuismer, S. L.Thompson, J. N. 2003 Coevolution in variable mutualismsAmerican Naturalist 162 S80CrossRefGoogle ScholarPubMed
Gomulkiewicz, R.Thompson, J. N.Holt, R. D.Nuismer, S. L.Hochberg, M. E. 2000 Hot spots, cold spots, and the geographic mosaic theory of coevolutionAmerican Naturalist 156 156CrossRefGoogle ScholarPubMed
Hougen-Eitzman, D.Rausher, M. D. 1994 Interactions between herbivorous insects and plant-insect coevolutionAmerican Naturalist 143 677CrossRefGoogle Scholar
Inouye, B.Stinchcombe, J. R. 2001 Relationships between ecological interaction modifications and diffuse coevolution: similarities, differences, and causal linksOikos 95 353CrossRefGoogle Scholar
Iwao, K.Rausher, M. D. 1997 Evolution of plant resistance to multiple herbivores: quantifying diffuse coevolutionAmerican Naturalist 149 316CrossRefGoogle Scholar
Janzen, D. H. 1980 When is it coevolutionEvolution 34 611CrossRefGoogle ScholarPubMed
Juenger, T.Bergelson, J. 1998 Pairwise versus diffuse natural selection and the multiple herbivores of scarlet gilia, Evolution 52 1583CrossRefGoogle Scholar
Leimu, R.Koricheva, J. 2006 A meta-analysis of genetic correlations between plant resistances to multiple enemiesAmerican Naturalist 168 E15CrossRefGoogle ScholarPubMed
Morris, W. F.Hufbauer, R. A.Agrawal, A. A. 2007 Direct and interactive effects of enemies and mutualists on plant performance: a meta-analysisEcology 88 1021CrossRefGoogle ScholarPubMed
Nuismer, S. L. 2006 Parasite local adaptation in a geographic mosaicEvolution 60 24CrossRefGoogle Scholar
Nuismer, S. L.Doebeli, M. 2004 Genetic correlations and the coevolutionary dynamics of three-species systemsEvolution 58 1165CrossRefGoogle ScholarPubMed
Nuismer, S. L.Gandon, S. 2008 Moving beyond common-garden and transplant designs: insight into the causes of local adaptation in species interactionsAmerican Naturalist 171 658Google ScholarPubMed
Nuismer, S. L.Thompson, J. N.Gomulkiewicz, R. 1999 Gene flow and geographically structured coevolutionProceedings of the Royal Society of London, Series B 266 605CrossRefGoogle Scholar
Nuismer, S. L.Thompson, J. N.Gomulkiewicz, R. 2000 Coevolutionary clines across selection mosaicsEvolution 54 1102CrossRefGoogle ScholarPubMed
Peacor, S. D.Werner, E. E. 1997 Trait-mediated indirect interactions in a simple aquatic food webEcology 78 1146CrossRefGoogle Scholar
Pellmyr, O.Thompson, J. N.Brown, J. M.Harrison, R. G. 1996 Evolution of pollination and mutualism in the yucca moth lineageAmerican Naturalist 148 827CrossRefGoogle Scholar
Pilson, D. 1996 Two herbivores and constraints on selection for resistance in Evolution 50 1492CrossRefGoogle Scholar
Rausher, M. 1996 Genetic analysis of coevolution between plants and their natural enemiesTrends in Genetics 12 212CrossRefGoogle ScholarPubMed
Ridenhour, B. J. 2005 Identification of selective sources: partitioning selection based on interactionsAmerican Naturalist 166 12CrossRefGoogle ScholarPubMed
Ridenhour, B. J.Nuismer, S. L. 2007 Polygenic traits and parasite local adaptationEvolution 61 368CrossRefGoogle ScholarPubMed
Stanton, M. L. 2003 Interacting guilds: moving beyond the pairwise perspective on mutualismsAmerican Naturalist 162 S10CrossRefGoogle ScholarPubMed
Stinchcombe, J. R.Rausher, M. D. 2001 Diffuse selection on resistance to deer herbivory in the ivyleaf morning glory, American Naturalist 158 376CrossRefGoogle Scholar
Stinchcombe, J. R.Rausher, M. D. 2002 The evolution of tolerance to deer herbivory: Modifications caused by the abundance of insect herbivoresProceedings of the Royal Society of London, Series B 269 1241CrossRefGoogle ScholarPubMed
Strauss, S. Y. 1991 Direct, indirect, and cumulative effects of three native herbivores on a shared host plantEcology 72 543CrossRefGoogle Scholar
Strauss, S. Y.Irwin, R. E. 2004 Ecological and evolutionary consequences of multispecies plant-animal interactionsAnnual Review of Ecology, Evolution, and Systematics 35 435CrossRefGoogle Scholar
Strauss, S. Y.Sahli, H.Conner, J. K. 2005 Toward a more trait-centered approach to diffuse (co)evolutionNew Phytologist 165 81CrossRefGoogle Scholar
Thompson, J. N. 1982 Interaction and CoevolutionNew YorkWileyCrossRefGoogle Scholar
Thompson, J. N. 1988 Variation in interspecific interactionsAnnual Review of Ecology and Systematics 19 65CrossRefGoogle Scholar
Thompson, J. N. 1994 The Coevolutionary ProcessChicago, ILUniversity of Chicago PressCrossRefGoogle Scholar
Thompson, J. N. 1998 The population biology of coevolutionResearches on Population Ecology 40 159CrossRefGoogle Scholar
Thompson, J. N. 2005 The Geographic Mosaic of CoevolutionChicago, ILUniversity of Chicago PressGoogle Scholar
Thompson, J. N.Cunningham, B. M. 2002 Geographic structure and dynamics of coevolutionary selectionNature 417 735CrossRefGoogle ScholarPubMed
Thompson, J. N.Pellmyr, O. 1992 Mutualism with pollinating seed parasites amid co-pollinators: constraints on specializationEcology 73 1780CrossRefGoogle Scholar
Werner, E. E.Peacor, S. D. 2003 A review of trait-mediated indirect interactions in ecological communitiesEcology 84 1083CrossRefGoogle Scholar
Wise, M. J.Sacchi, C. F. 1996 Impact of two specialist insect herbivores on reproduction of horse nettle, Oecologia 108 328CrossRefGoogle Scholar
Wootton, J. T. 1993 Indirect effects and habitat use in an intertidal community – interaction chains and interaction modificationsAmerican Naturalist 141 71CrossRefGoogle Scholar
Zangerl, A. R.Berenbaum, M. R. 2003 Phenotype matching in wild parsnip and parsnip webworms: causes and consequencesEvolution 57 806CrossRefGoogle ScholarPubMed

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