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Simulating Herbivory: Problems and Possibilities

  • J. Hjältén
Part of the Ecological Studies book series (ECOLSTUD, volume 173)

Summary

Much of our knowledge of plant—herbivore interactions are based on results from experiments applying mechanical damage to plants. However, in recent years, the use of simulated herbivory has been criticized and several problems identified. The aim of this chapter is therefore to identify the most obvious advantages and disadvantages of using simulated insect herbivory and suggest ways to avoid some of the problems or alternative ways to conduct the experiments, e.g. by using natural herbivores caged on specific plant parts (clip cages).

It is clear from the literature that simulated herbivory often fails to induce plant responses that are important for complex biotic interaction, e.g. interactions between plants, different insect herbivore species and their predators/parasites. This strongly suggests that if the aim of a study is to identify and understand the ecological role of these complex interactions and ecosystem processes we need to use natural herbivory. Simulated herbivory may, however, still be an appropriate method for investigating simple biotic interactions, e.g. the effects of herbivory on plant growth and survival or physiological processes in plants that deter or limit further herbivory by the same herbivore. Simulated herbivory might also be a useful tool for dissecting damage into its functional parts, i.e. mechanical wounding and elicitor application.

The study of more complex biotic interactions, e.g. plant-mediated competition or interactions involving a third tropic level, requires the activity of real herbivores. Nevertheless, we should be aware that even the use of natural herbivory is associated with potential problems, e.g. clip cages can reduce radiation, increase leaf temperature, reduce leaf expansion and restrict realistic interactions with predators and parasites, and this should be taken into account when designing experiments and interpreting results.

Keywords

Biotic Interaction Wild Radish Clip Cage Induce Plant Response Caterpillar Species 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Agrawal A (2000a) Specificity of induced responses in wild radish: causes and consequences for two specialist and two generalist caterpillars. Oikos 89: 493–500CrossRefGoogle Scholar
  2. Agrawal A (2000b) Benefits and costs of induced plant defence for Lepidium virginicum (Brassicaceae). Ecology 81: 1804–1813CrossRefGoogle Scholar
  3. Agrawal A (2002) Herbivory and maternal effects: mechanisms and consequences of transgenerational induced resistance. Ecology 83: 3408–3415CrossRefGoogle Scholar
  4. Bach CE (1994) Effects of herbivory on growth and survivorship of sand-dune willow (Salix cordata). Ecol Entomol 19: 303–309CrossRefGoogle Scholar
  5. Baldwin IT (1990) Herbivory simulations in ecological research. TREE 5: 91–93PubMedGoogle Scholar
  6. Baldwin IT, Preston CA (1999) The eco-physiological complexity of plant responses to insect herbivores. Planta 208: 137–145CrossRefGoogle Scholar
  7. Baldwin IT, Kessler A, Halitschke R (2002) Volatile signalling in plant–plant-interactions: what is real? Curr Opin Plant Biol 5: 1–4CrossRefGoogle Scholar
  8. Bardgett RD, Wardle DA, Yeates GW (1998) Linking above-ground and below-ground interactions: how plant responses to foliar herbivory influence soil organisms. Soil Biol Biochem 30: 1867–1878CrossRefGoogle Scholar
  9. Belowsky G, Slade JB (2000) Insect herbivory accelerates nutrient cycling and increases plant production. Proc Natl Acad Sci USA 97: 14412–14417CrossRefGoogle Scholar
  10. Belowsky G, Slade JB (2002) An ecosystem perspective on grasshopper control: possible advantages to no treatment. J Orthop Res 11: 29–35CrossRefGoogle Scholar
  11. Bergman M (2002) Can saliva from moose, Alces alces, affect growth responses in the sallow, Salix caprea? Oikos 96: 164–168CrossRefGoogle Scholar
  12. Bergström R, Danell K (1995) Effect of simulated summer browsing by moose on leaf and shoot biomass of birch, Betula pendula. Oikos 72: 132–138Google Scholar
  13. Cargill SM, Jefferies RL (1984) The effects of grazing by lesser snow geese on the vegetation of a sub-arctic salt marsh. J Appl Ecol 21: 669–686CrossRefGoogle Scholar
  14. Craft-Brandner SJ, Chu C-C (1999) Insect clip cages rapidly alters photosynthetic traits of leaves. Crop Sci 39: 1896–1899CrossRefGoogle Scholar
  15. Danell K, Huss-Danell K, Bergström R (1985) Interactions between browsing moose and two species of birch in Sweden. Ecology 66: 1867–1878CrossRefGoogle Scholar
  16. de Mazancourt C, Loreau M, Abbadie L (1998) Grazing optimization and nutrient cycling: when do herbivores enhance plant production? Ecology 79: 2242–2252CrossRefGoogle Scholar
  17. Després L (2003) Sex and pollen: the role of males in stabilising a plant–seed eater pollinating mutualism. Oecologia 135: 60–66CrossRefPubMedGoogle Scholar
  18. Dodd RL, Linhart YB (1994) Reproductive consequences of interactions between Yucca glauca (Agavaceae) and Tegeticula yuccasella ( Lepidoptera) in Colorado. Am J Bot 81: 815–825Google Scholar
  19. Escarré J, Lepart J, Sentuc JJ (1996) Effect on simulated herbivory in three old field Compositae with different inflorescence architecture. Oecologia 105: 501–508CrossRefGoogle Scholar
  20. Gomez JM, Gonzáles-Megías A (2002) Asymmetrical interactions between ungulates and phytophagous insects: being different matters. Ecology 83: 203–211CrossRefGoogle Scholar
  21. Hättenschwiler S, Vitousek PM (2002) The role of polyphenols in terrestrial ecosystem nutrient cycling. TREE 15: 238–243Google Scholar
  22. Hjältén J (1999) Interspecific variation in willow response to pruning: the effect on plant growth, survival and susceptibility to leaf-gallers. Ecoscience 6: 62–67Google Scholar
  23. Hjältén J, Price PW (1996) The effect of pruning on plant growth and sawfly population densities. Oikos 77: 549–555CrossRefGoogle Scholar
  24. Hjältén J, Danell K, Ericson L (1993) Effect of simulated herbivory and intraspecific competition on the compensatory ability of juvenile birches. Ecology 74: 1136–1142CrossRefGoogle Scholar
  25. Hobbs NT (1996) Modifications of ecosystems by ungulates. J Wildl Manage 60: 695–713CrossRefGoogle Scholar
  26. Honkanen T, Haukioja E (1994) Why does a branch suffer more after branch-wide than after tree-wide defoliation? Oikos 71: 441–450CrossRefGoogle Scholar
  27. Honkanen T, Haukioja E (1998) Intra-plant regulation of growth and plant–herbivore interactions. Ecoscience 5: 470–479CrossRefGoogle Scholar
  28. Honkanen T, Haukioja E, Kitunen V (1999) Responses of Pinus sylvestris to simulated herbivory are modified by tree sink/source dynamics and by external resources. Funct Ecol 13: 126–140CrossRefGoogle Scholar
  29. Kahl J, Siemens DH, Aerts RJ, Gaebler R, Kuehnemann F, Preston CA, Baldwin IT (2000) Herbivore-induced ethylene suppresses a direct defence but not a putative indirect defence against an adapted herbivore. Planta 210: 336–342CrossRefPubMedGoogle Scholar
  30. Kielland K, Bryant JP (1998) Moose herbivory in taiga: effects on biochemistry and vegetation dynamics in primary succession. Oikos 82: 377–383CrossRefGoogle Scholar
  31. Krupnick GA, Avila G, Brown KM, Stephenson AG (2000) Effects of herbivory on ethyl- ene production and sex expression in Curcurbita texana. Funct Ecol 14: 215–225CrossRefGoogle Scholar
  32. McCloud ES, Baldwin IT (1997) Herbivory and caterpillar regurgitants amplify the wound-induced increase in jasmonic acid but not nicotine in Nicotiana sylvestris. Planta 203: 430–435CrossRefGoogle Scholar
  33. Moore JP, Taylor JE, Pual ND, Whittaker JB (2003) The use of clip cages to restrain insects reduces leaf expansion systematically in Rumex obtusifolius. Ecol Entomol 28: 239–242CrossRefGoogle Scholar
  34. Musser RO, Hum-Musser SM, Eichenseer H, Peiffer M, Erwin G, Murphy JB, Felton GW (2002) Caterpillar saliva beats plant defenses. Nature 416: 599–600CrossRefPubMedGoogle Scholar
  35. Nefdt RJC, Compton SG (1996) Regulation of seed and pollinator production in the fig wasp mutualism. J Anim Ecol 65: 170–182CrossRefGoogle Scholar
  36. Obeso JR, Grubb PJ (1994) Interactive effects of the extent and timing of defoliation and nutrient supply on reproduction in a chemically defended annual Senecio vulgaris. Oikos 71: 506–514CrossRefGoogle Scholar
  37. Oesterheld M, McNaughton SJ (1991) Effect of stress and time for recovery on the amount of compensatory growth after grazing. Oecologia 85: 305–313CrossRefGoogle Scholar
  38. Orians CM, Griffiths M, Roche B, Fritz R (2000) Phenolic glucosides and condensed tannins in Salix sericea, S. eriocephala and their F1 hybrids: not all hybrids are created equal. Biochem Syst Ecol 28: 619–632CrossRefPubMedGoogle Scholar
  39. Paige KN, Whitham TG (1987) Overcompensation in response to mammalian herbivory–the advantage of being eaten.Am Nat 129: 407–416Google Scholar
  40. Pastor J, Dewey B, Naiman RJ, McInnes PF, Cohen Y (1993) Moose browsing and soil fertility in the boreal forest of Isle Royale National Park. Ecology 74: 467–480CrossRefGoogle Scholar
  41. Persson I-L (2003) Moose density and habitat productivity as drivers of ecosystem processes in northern boreal forests. PhD Thesis, Swedish University of Agricultural Sciences, UmeåGoogle Scholar
  42. Pilson D, Decker KL (2002) Compensation for herbivory in wild sunflower: response to simulated damage by the head-clipping weevil. Ecology 83: 3097–3107CrossRefGoogle Scholar
  43. Price PW, Clancy KM, Roininen H (1994) Comparative population dynamics of the galling sawflies. In: Price PW, Mattson WJ, Baranchikov YN (eds) The ecology and evolution of gall-forming insects. North Central Forest Experiment Station General Tech Rep NC-174. US Department of Agriculture, Forest Service, St Paul, Minnesota, pp 1–11Google Scholar
  44. Rand TA (1999) Effect of environmental context on the susceptibility of Atriplex patula to attack by herbivorous beetles. Oecologia 121: 39–46CrossRefGoogle Scholar
  45. Reynolds BC, Hunter MD (2001) Responses of soil respirations, soil nutrients and litter decomposition to inputs from canopy herbivores. Soil Biol Biochem 33: 1641–1652CrossRefGoogle Scholar
  46. Sadras VO (1998) Herbivory tolerance of cottons expressing insecticidal proteins from Bacillus thuringiensis: response to damage caused by Helicoverpa spp. and to manual bud removal. Field Crop Res 56: 287–299CrossRefGoogle Scholar
  47. Schmitz OJ (2003) Top predator control of plant biodiversity and productivity in an old-field ecosystem. Ecol Lett 6: 156–163CrossRefGoogle Scholar
  48. Snyder WE, Wise DH (2001) Contrasting trophic cascades generated by a community of generalist predators. Ecology 82: 1571–1583CrossRefGoogle Scholar
  49. Strauss SY (199 1) Direct, indirect, and cumulative effects of three native herbivores on a shared host plant. Ecology 72:543–558Google Scholar
  50. Thaler JS, Fidantsef AL, Bostock RM (2002) Antagonism between jasmonate-and salicylate-mediated induced plant resistance: effects of concentration and timing of elicitation on defense-related proteins, herbivores, and pathogen performance in tomato. J Chem Ecol 28: 1131–1159CrossRefPubMedGoogle Scholar
  51. Tiffin P (2002) Competition and time of damage affect the pattern of selection acting on plant defence against herbivores. Ecology 83: 1981–1990CrossRefGoogle Scholar
  52. Tiffin P, Inouye BD (2000) Measuring tolerance to herbivory: accuracy and precision of estimates made using natural versus imposed damage. Evolution 54: 1024–1029CrossRefPubMedGoogle Scholar
  53. Tolvanen A, Laine K, Pakonen T, Saari E, Havas P (1993) Effect of habitat and time of clipping on the recovery of the bilberry ( Vaccinium myrtillus ). Ann Bot Fenn 30: 15–20Google Scholar
  54. Tscharntke T, Thiessen S, Dolch R, Boland W (2001) Herbivory induced resistance and interplant signal transfer in Alnus glutinosa. Biochem Syst Ecol 29: 1025–1047CrossRefGoogle Scholar
  55. Turlings TCJ, Lengwiler UB, Bernasconi ML, Wechsler D (1998) Timing of volatile emission in maize seedlings. Planta 207: 146–152CrossRefGoogle Scholar
  56. Waltz AM, Whitham TG (1997) Plant development affects arthropod communities: opposing impact on species removal. Ecology 78: 2133–2144CrossRefGoogle Scholar

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© Springer-Verlag Berlin Heidelberg 2008

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  • J. Hjältén

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