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3 - Going with the flow: plant vascular systems mediate indirect interactions between plants, insect herbivores, and hemi-parasitic plants

Published online by Cambridge University Press:  12 August 2009

Susan E. Hartley
Affiliation:
University of Sussex
Kathy A. Bass
Affiliation:
University of Sussex
Scott N. Johnson
Affiliation:
University of Reading
Takayuki Ohgushi
Affiliation:
Kyoto University, Japan
Timothy P. Craig
Affiliation:
University of Minnesota, Duluth
Peter W. Price
Affiliation:
Northern Arizona University
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Summary

Introduction

Plant-mediated indirect interactions between phytophagous insects

There is increasing interest in the consequences of indirect interactions for community structure and function (Wootton 1994). Herbivory by one phytophagous species has the potential to affect other herbivores exploiting the same plant, hence plants are able to mediate indirect interactions between organisms that exploit them, even if these organisms are spatially or temporally separated (Masters and Brown 1997). For example, root-feeding herbivores may impact on the performance of foliar feeding insects (Gange and Brown 1989, Masters and Brown 1992), while herbivores feeding early in the season affect the growth and development of those feeding later (West 1985, Harrison and Karban 1986). Many such interactions are mediated by damage-induced changes in the chemical composition of the shared host plant (Hartley and Jones 1997, Karban and Baldwin 1997), particularly increases in secondary compounds (Hartley and Lawton 1987, Haukioja et al. 1990), but there are also cases where alterations in the nutrient levels within the host explain the impact of one insect herbivore on another (McClure 1980, Denno et al. 2000). Thus both changes in nutrient and in secondary compounds have been associated with detrimental effects on other phytophagous insects and may underpin competitive indirect interactions between herbivores (Denno et al. 1995).

The importance of competitive interactions between phytophagous insects has been re-evaluated in recent years.

Type
Chapter
Information
Ecological Communities
Plant Mediation in Indirect Interaction Webs
, pp. 51 - 74
Publisher: Cambridge University Press
Print publication year: 2007

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References

Abrahamson, W. G., and McCrea, K. D.. 1986. Nutrient and biomass allocation in Solidago altissima: effects of two stem gall-makers, fertilisation and ramet isolation. Oecologia 68:174–180.CrossRefGoogle Scholar
Awmack, C. S., and Leather, S. R.. 2002. Host plant quality and fecundity in herbivorous insects. Annual Review of Entomology 47:817–844.CrossRefGoogle ScholarPubMed
Bass, K. A. 2004. Resource partitioning in the multi-species interaction between a host plant, a parasitic angiosperm and an insect herbivore. Ph.D. dissertation, University of Sussex, Brighton, UK.
Bigger, D. S., and Marvier, M. A.. 1998. How different would a world without herbivory be? A search for generality in ecology. Integrative Biology 1:60–67.3.0.CO;2-Z>CrossRefGoogle Scholar
Blossey, B., and Hunt-Joshi, T. R.. 2003. Belowground herbivory by insects: influence on plants and aboveground herbivores. Annual Review of Entomology 48:521–547.CrossRefGoogle ScholarPubMed
Bonsall, M. B., and Hassell, M. P.. 1997. Apparent competition structures ecological assemblages. Nature 388:371–373.CrossRefGoogle Scholar
Bowling, D. J. F., and Dunlop, J.. 1978. Uptake of phosphate by white clover. I. Evidence for an electrogenic phosphate pump. Journal of Experimental Botany 29:1139–1146.CrossRefGoogle Scholar
Brown, V. K., and Gange, A. C.. 1992. Secondary plant succession: how is it modified by insect herbivory?Vegetatio 101:3–13.CrossRefGoogle Scholar
Carroll, C. R., and Hoffman, C. A.. 1980. Chemical feeding deterrent mobilized in response to insect herbivory and counteradaptation by Epilachna tredecimnotata. Science 209:414–416.CrossRefGoogle ScholarPubMed
Cechin, I., and Press, M. C.. 1993. Nitrogen relations of the sorghum–Striga hermonthica host–parasite association: growth and photosynthesis. Plant, Cell and Environment 16:237–247.CrossRefGoogle Scholar
Choudhury, D. 1984. Aphids and plant fitness: a test of Owen and Weigert's hypothesis. Oikos 43:401–402.CrossRefGoogle Scholar
Clay, K. 1988. Fungal endophytes of grasses: a defensive mutualism between plants and fungi. Ecology 69:10–16.CrossRefGoogle Scholar
Connor, E. F., and Taverner, M. P.. 1997. The evolution and adaptive significance of the leaf-mining habit. Oikos 79:6–25.CrossRefGoogle Scholar
Crawley, M. J. 1983. Herbivory: The Dynamics of Animal–Plant Interactions. Oxford, UK: Blackwell Science.Google Scholar
Davies, D. M., and Graves, J. D.. 2000. The impact of phosphorus on interactions of the hemi-parasitic angiosperm Rhinanthus minor and its host Lolium perenne. Oecologia 124:100–106.CrossRefGoogle Scholar
Denno, R. F., and Roderick, G. K.. 1992. Density-related dispersal in plant hoppers: effects of interspecific crowding. Ecology 73:1323–1334.CrossRefGoogle Scholar
Denno, R. F., McClure, M. S., and Ott, J. R.. 1995. Interspecific interactions in phytophagous insects: competition re-examined and resurrected. Annual Review of Entomology 40:297–331.CrossRefGoogle Scholar
Denno, R. F., Peterson, M. A., Gratton, C., Cheng, J., Langellotto, G. A., Huberty, A. F., and Finke, D. L.. 2000. Feeding-induced changes in plant quality mediate interspecific competition between sap-feeding herbivores. Ecology 81:1814–1827.CrossRefGoogle Scholar
Dixon, A. F. G. 1998. Aphid Ecology: An Optimization Approach, 2nd edn. London: Chapman and Hall.Google Scholar
Dussourd, D. E., and Denno, R. F.. 1994. Host range of generalist caterpillars: trenching permits feeding on plants with secretory canals. Ecology 75:69–78.CrossRefGoogle Scholar
Dussourd, D. E., and Eisner, T.. 1987. Vein cutting behavior: insect counterploy to the latex defense of plants. Science 237:898–901.CrossRefGoogle Scholar
Fellows, R. J., and Geiger, D. R.. 1974. Structural and physiological changes in sugar beet leaves during sink to source conversion. Plant Physiology 54:877–885.CrossRefGoogle ScholarPubMed
Fisher, A. E. I., Hartley, S. E., and Young, M.. 2000. Direct and indirect competitive effects of foliage feeding guilds on the performance of the birch leaf-miner Eriocrania. Journal of Animal Ecology 69:165–176.CrossRefGoogle Scholar
Forcella, F. 1982. Why twig-girdling beetles girdle twigs. Naturwissenschaften 69:398–400.CrossRefGoogle Scholar
Fraser, L. H., and Grime, J. P.. 1999. Aphid fitness on 13 grass species: a test of plant defence theory. Canadian Journal of Botany 77:1783–1789.CrossRefGoogle Scholar
Fukui, A. 2001. Indirect interactions mediated by leaf shelters in animal–plant communities. Population Ecology 43:31–40.CrossRefGoogle Scholar
Gange, A. C., and E. Bower. 1997. Interactions between insects and mycorrhizal fungi, pp. 115–132 in Gange, A. C. and Brown, V. K. (eds.) Multitrophic Interactions in Terrestrial Systems. Oxford, UK: Blackwell Science.Google Scholar
Gange, A. C., and Brown, V. K.. 1989. Effects of root herbivory by an insect on a foliar-feeding species, mediated through changes in the host plant. Oecologia 81:38–42.CrossRefGoogle ScholarPubMed
Graves, J. D. 1995. Host-plant responses to parasitism, pp. 207–225 in Press, M. C. and Graves, J. D. (eds.) Parasitic Plants. London: Chapman and Hall.Google Scholar
Graves, J. D., Press, M. C., and Stewart, G. R.. 1989. A carbon balance model of the sorghum–Striga hermonthica host–parasite association. Plant, Cell and Environment 12:101–107.CrossRefGoogle Scholar
Graves, J. D., Wylde, A., Press, M. C., and Stewart, G. R.. 1990. Growth and carbon allocation in Pennisetum typhoides infected with the parasitic angiosperm Striga hermonthica. Plant, Cell and Environment 13:367–373.Google Scholar
Graves, J. D., Press, M. C., Smith, S., and Stewart, G. R.. 1992. The carbon economy of the association between cowpea and the parasitic angiosperm Striga gesnerioides. Plant, Cell and Environment 13:319–328.Google Scholar
Hajek, A. E., and Dahlsten, D. L.. 1986. Discriminating patterns of variation in aphid (Homoptera, Drepanosiphidae) distribution on Betula pendula. Environmental Entomology 15:1145–1148.CrossRefGoogle Scholar
Harrison, S., and Karban, R.. 1986. Effects of an early season folivorous moth on the success of a later season species, mediated by a change in quality of the shared host, Lupinus arboreus Sims. Oecologia 69:354–359.CrossRefGoogle ScholarPubMed
Hartley, S. E. 1998. The chemical composition of plant galls: are levels of nutrients and secondary compounds controlled by the gall-former?Oecologia 113:492–501.CrossRefGoogle ScholarPubMed
Hartley, S. E., and C. G. Jones. 1997. Plant chemistry and herbivory, or why the world is green, pp. 284–324 in Crawley, M. J. (ed.) Plant Ecology. Oxford, UK: Blackwell Science.Google Scholar
Hartley, S. E., and T. H. Jones. 2004. Insect herbivores, nutrient cycling and plant productivity: a review, pp. 27–52 in Weisser, W. W. and Siemann, E. (eds.) Insects and Ecosystem Function. Berlin, Germany: Springer-Verlag.Google Scholar
Hartley, S. E., and Lawton, J. H.. 1987. Effects of different types of damage on the chemistry of birch foliage, and the responses of birch feeding insects. Oecologia 74:432–437.CrossRefGoogle ScholarPubMed
Hartley, S. E., and Lawton, J. H.. 1992. Host-plant manipulation by gall insects: a test of the nutrition hypothesis. Journal of Animal Ecology 61:113–119.CrossRefGoogle Scholar
Hartley, S. E., Gardner, S. M., and Mitchell, R. J.. 2003. Indirect effects of grazing and nutrient addition on the hemipteran community of heather moorlands. Journal of Applied Ecology 40:793–803.CrossRefGoogle Scholar
Hatcher, P. E. 1995. Three-way interactions between plant pathogenic fungi, herbivorous insects and their host plants. Biological Reviews 70:639–694CrossRefGoogle Scholar
Haukioja, E., Ruohomaki, K., Senn, J., Suomela, J., and Walls, M.. 1990. Consequences of herbivory in the mountain birch (Betula pubescens ssp. tortuosa): importance of the functional organization of the tree. Oecologia 82:238–247.CrossRefGoogle ScholarPubMed
Inbar, M., Eshel, A., and Wool, D.. 1995. Interspecific competition among phloem-feeding insects mediated by induced host-plant sinks. Ecology 76:1506–1515.CrossRefGoogle Scholar
Jiang, F., Jeschke, W. D., and Hartung, W.. 2004. Solute flows from Hordeum vulgare to the hemiparasite Rhinanthus minor and the influence of infection on host and parasite nutrient relations. Functional Plant Biology 31:633–643.CrossRefGoogle Scholar
Johnson, S. N., Mayhew, P. J., Douglas, A. E., and Hartley, S. E.. 2002. Insects as leaf engineers: can leaf-miners alter leaf structure for birch aphids?Functional Ecology 16:575–584.CrossRefGoogle Scholar
Johnson, S. N., Douglas, A. E., Woodward, S., and Hartley, S. E.. 2003. Microbial impacts on plant–herbivore interactions: the indirect effects of a birch pathogen on a birch aphid. Oecologia 134:388–396.CrossRefGoogle ScholarPubMed
Karban, R. 1986. Interspecific competition between folivorous insects on Erigeron glaucus. Ecology 67:1063–1072.CrossRefGoogle Scholar
Karban, R., and Baldwin, I. T.. 1997. Induced Responses to Herbivory. Chicago, IL: University of Chicago Press.CrossRefGoogle Scholar
Kennedy, J. S. 1951. Benefits to aphids from feeding on galled and virus-infected leaves. Nature 168:825–826.CrossRefGoogle ScholarPubMed
Larson, K. C., and Whitham, T. G.. 1991. The manipulation of food resources by a gall-forming aphid: the physiology of sink–source interactions. Oecologia 88:15–21.CrossRefGoogle ScholarPubMed
Larson, K. C., and Whitham, T. G.. 1997. Competition between gall aphids and natural plant sinks: plant architecture affects resistance to galling. Oecologia 109:575–582.CrossRefGoogle ScholarPubMed
Lawton, J. H., and Hassell, M. P.. 1981. Asymmetrical competition in insects. Nature 289:793–795.CrossRefGoogle Scholar
Louda, S. M., K. H. Keeler, and R. D. Holt. 1990. Herbivore influences on plant performance and competitive interactions, pp. 413–444 in Grace, J. B. and Tilman, D. (eds.) Perspectives in Plant Competition. London: Academic Press.Google Scholar
Martin, M. A., Cappuccino, N., and Ducharme, D.. 1994. Performance of Symydobius americanus (Homoptera, Aphididae) on paper birch grazed by caterpillars. Ecological Entomology 19:6–10.CrossRefGoogle Scholar
Masters, G. J., and Brown, V. K.. 1992. Host plant mediated interactions between two spatially separated insects. Functional Ecology 6:175–179.CrossRefGoogle Scholar
Masters, G. J., and V. K. Brown. 1997. Host-plant mediated interactions between spatially separated herbivores: effects on community structure, pp. 217–237 in Gange, A. C. and Brown, V. K. (eds.) Multitrophic Interactions in Terrestrial Systems. Oxford, UK: Blackwell Science.Google Scholar
Mattson, W. J. 1986. Competition for food between two principal cone insects of red pine, Pinus resinosa. Environmental Entomology 15:88–92.CrossRefGoogle Scholar
McClure, M. S. 1980. Competition between exotic species: scale insects on hemlock. Ecology 61:1391–1401.CrossRefGoogle Scholar
Meyer, G. A. 1993. A comparison of leaf and sap feeding insects on photosynthetic rates of goldenrod. Oecologia 92:480–489.CrossRefGoogle Scholar
Nakamura, M., and Ohgushi, T.. 2003. Positive and negative effects of leaf shelters on herbivorous insects: linking multiple herbivore species on willow. Oecologia 136:445–449.CrossRefGoogle ScholarPubMed
Pennings, S. C., and Callaway, R. M.. 2002. Parasitic plants: parallels and contrasts with herbivores. Oecologia 131:479–489.CrossRefGoogle ScholarPubMed
Petersen, M. K., and Sandstrom, J. P.. 2001. Outcome of indirect competition between two aphid species mediated by responses in their common host plant. Functional Ecology 15:525–534.CrossRefGoogle Scholar
Press, M. C., and Seel, W. E.. 1996. Interactions between hemiparasitic angiosperms and their hosts in the subarctic. Ecological Bulletins 45:151–158.Google Scholar
Press, M. C., J. D. Scholes, and J. R. Watling. 1998. Parasitic plants: physiological and ecological interactions with their hosts, pp. 174–197 in Press, M. C., Scholes, J. D., and Barker, M. G. (eds.) Physiological Plant Ecology. Oxford, UK: Blackwell Science.Google Scholar
Prestidge, R. A., and McNeil, S.. 1982. The role of nitrogen in the ecology of grassland Auchenorrhyncha (Homoptera). Symposium of the British Ecological Society 22:257–281.Google Scholar
Price, P. W., and Louw, S.. 1996. Resource manipulation through architectural modification of the host plant by a gall-forming weevil Urodontus scholtzi Louw (Coleoptera: Anthribidae). African Entomology 4:103–110.Google Scholar
Price, P. W., G. W. Fernandes, and R. DeClerck-Floate. 1997. Gall-inducing insect herbivores in multitrophic systems, pp. 239–255 in Gange, A. C. and Brown, V. K. (eds.) Multitrophic Interactions in Terrestrial Systems. Oxford, UK: Blackwell Science.Google Scholar
Puustinen, S., and Mutikainen, P.. 2001. Host–parasite–herbivore interactions: implications of host cyanogenesis. Ecology 82:2059–2071.Google Scholar
Puustinen, S., and Salonen, V.. 1999. The effect of host defoliation on hemiparasitic-host interactions between Rhinanthus serotinus and two Poa species. Canadian Journal of Botany 77:523–530.CrossRefGoogle Scholar
Pywell, R. F., Bullock, J. M., Walker, K. J., Coulson, S. J., Gregory, S. J., and Stevenson, M. J.. 2004. Facilitating grassland diversification using the hemiparasitic plant Rhinanthus minor. Journal of Applied Ecology 41:880–887.CrossRefGoogle Scholar
Quested, H. M., Press, M. C., Callaghan, T. V., and Cornelissen, J. H. C.. 2002. The hemiparasitic angiosperm Bartsia alpina has the potential to accelerate decomposition in sub-arctic communities. Oecologia 130:88–95.CrossRefGoogle ScholarPubMed
Ramlan, M. F., and Graves, J. D.. 1996. Estimation of the sensitivity to photoinhibition in Striga hermonthica-infected sorghum. Journal of Experimental Botany 47:71–78.CrossRefGoogle Scholar
Raven, J. A. 1983. Phytophages of xylem and phloem: a comparison of animal and plant sap-feeders. Advances in Ecological Research 13:135–234.CrossRefGoogle Scholar
Seel, W. E., and Jeschke, W. D.. 1999. Simultaneous collection of xylem sap from Rhinanthus minor and the hosts Hordeum and Trifolium: hydraulic properties, xylem sap composition and effects of attachment. New Phytologist 143:281–298.CrossRefGoogle Scholar
Seel, W. E., and Press, M. C.. 1996. Effects of repeated parasitism by Rhinanthus minor on the growth and photosynthesis of a perennial grass, Poa alpina. New Phytologist 134:495–502.CrossRefGoogle Scholar
Seel, W. E., I. Cechin, C. A. Vincent, and M. C. Press. 1992. Carbon partitioning and transport in parasitic angiosperms and their hosts, pp. 199–223 in Pollock, C. J., Farrar, J. F., and Gordon, A. J. (eds.) Carbon Partitioning within and between Organisms. Oxford, UK: Bios.Google Scholar
Shorthouse, J. D., and Rohfritsch, O. (eds.) 1992. Biology of Insect-Induced Galls. New York: Oxford University Press.Google Scholar
Strauss, S. Y., and A. R. Zangerl. 2002. Plant–insect interactions in terrestrial ecosystems, pp. 77–106 in Herrera, C. M. and Pellmyr, O. (eds.) Plant–Animal Interactions: An Evolutionary Approach. Oxford, UK: Blackwell Science.Google Scholar
Strong, D. R., Lawton, J. H., and Southwood, T. R. E.. 1984. Insects on Plants: Community Patterns and Mechanisms. Oxford, UK: Blackwell Science.Google Scholar
Voss, T. C., Kieckefer, R. W., Fuller, B. W., Mcleod, M. J., and Beck, D. A.. 1997. Yield losses in maturing spring wheat caused by cereal aphids (Homoptera: Aphididae) under laboratory conditions. Journal of Economic Entomology 90:1346–1350.CrossRefGoogle Scholar
Wangai, A. W., Plumb, R. T., and Emden, H. F.. 2000. Effects of sowing date and insecticides on cereal aphid populations and barley yellow dwarf virus on barley in Kenya. Journal of Phytopathology 148:33–37.CrossRefGoogle Scholar
West, C. 1985. Factors underlying the late seasonal appearance of the lepidopterous leaf-mining guild on oak. Ecological Entomology 10:111–120.CrossRefGoogle Scholar
White, T. C. R. 1984. The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants. Oecologia 63:90–105.CrossRefGoogle ScholarPubMed
Wool, D., Aloni, R., Ben-Zvi, O., and Wollberg, M.. 1999. A galling aphid furnishes its home with a built-in pipeline to the host food supply. Entomologia Experimentalis et Applicata 91:183–186.CrossRefGoogle Scholar
Wootton, J. T. 1994. The nature and consequences of indirect effects in ecological communities. Annual Review of Ecology and Systematics 25:443–466.CrossRefGoogle Scholar
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