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Egg clumping, host plant selection and population regulation in Cactoblastis cactorum (Lepidoptera)

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Summary

Since the successful control of prickly pear cactus by Cactoblastis cactorum in Australia, populations of plants and moths have persisted at low densities in open woodland sites. A contagious egg distribution causes overcrowding of larvae on some plants but insures low levels or no attack of other plants. This prevents extinction of plants and insects. Cactoblastis moths choose plants with characteristics which may increase the success of their larvae. Field observations and cage experiments indicate that large, green cactuses near previously attacked cactuses receive more eggs. Plants which are actively photosynthesizing are also more attractive as oviposition sites. These oviposition preferences contribute to the observed contagious egg distribution.

While open woodland Opuntia and Cactoblastis populations fluctuate around an equilibrium, pasture populations may better be described by the “hide and seek” model, with the woodland populations serving as refuges. Average plant quality and variation in quality are suggested as important components in the dynamics of this system.

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References

  • Andrewartha HG, Birch LC (1954) The Distribution and Abundance of Animals. Chicago

  • Barbosa P, Greenblatt J (1979) Effects of leaf age and position on larval preferences of the fall webworm, Hyphantria cunea (Lepidoptera: Arctiidae). Can Ent 111:381–383

    Google Scholar 

  • Birch LC (1971) The role of environmental heterogeneity in determining distribution and abundance. In: PJ den Boer and GR Gradwell (eds) Proc Adv Study Inst Dynamics Numbers Popul. p 109–128

  • Chew FS (1977) Coevolution of Pierid butterflies and their cruciferous foodplants. II. the distribution of eggs on potential foodplants Evolution 31:568–579

    Google Scholar 

  • Dixon CA, Erickson JM, Kellert DN, Rothschild M (1978) Some adaptations between Danaus plexippus and its food plant, with notes on Danaus chrysippus and Euploea core. J Zool Lond 185:437–467

    Google Scholar 

  • Dodd AP (1940) The Biological Campaign Against Prickly Pear. Commonwealth Prickly Pear Board:Brisbane

    Google Scholar 

  • Holloway JK (1964) Projects in Biological Control of Weeds. In: P de Bach (ed) Biological Control of Insect Pests and Weeds. Chapman and Hall, London pp 650–670

    Google Scholar 

  • Ives PM (1978) How discriminating are cabbage butterflies? Aust J Ecol 3:261–276

    Google Scholar 

  • Jones RE, Ives PM (1979) The adaptiveness of searching and host selection behaviour in Pieris rapae (L.) Aust J Ecol 4:75–86

    Google Scholar 

  • Krebs CJ (1972) Ecology: The Experimental Analysis of Distribution and Abundance. Harper and Row, New York

    Google Scholar 

  • Mann J (1969) The Cactus-feeding Insects and Mites. Smithsonian Institute, Washington, D.C.. Bulletin 256

    Google Scholar 

  • Mann J (1970) Cacti Naturalized in Australia and Their Control. Department of Lands, Brisbane

    Google Scholar 

  • Mattson WJ (1980) Herbivory in relation to plant nitrogen content. Ann Rev Ecol Syst 11:119–161

    Google Scholar 

  • Monro J (1967) The exploitation and conservation of resources by populations of insects. J Anim Ecol 36:531–547

    Google Scholar 

  • Monro J (1975) Environmental variation and the efficiency of biological control—Cactoblastis in the Southern Hemisphere. In: J Kikkawa, HA Nix (eds) Managing Terrestrial Ecosystems. Proc Ecol Soc Australia 9:204–212

  • Myers JH (1980) Is the insect or the plant the driving force in the cinnabar moth—tansy ragwort system? Oecologia (Berl) 47:16–21

    Google Scholar 

  • Myers JH (1976) Distribution and dispersal in populations capable of resource depletion: a simulation model. Oecologia (Berl) 23:255–269

    Google Scholar 

  • Myers JH, Post B (1981) Plant nitrogen and insect population fluctuations: a test with the cinnabar moth-tansy ragwort system. Oecologia (Berl) 48:151–156

    Google Scholar 

  • Osmond CB, Nott DL, Firth PM (1979) Carbon assimilation patterns and growth of the introduced CAM plant Opuntia inermis in eastern Australia. Oecologia (Berl) 40:331–350

    Google Scholar 

  • Osmond CB, Monro J (1981) Prickly Pear. In: DJ Carr, SM Carr (eds) Plants and Man. Academic Press, Sydney, pp 194–222

    Google Scholar 

  • Price PW (1975) Insect Ecology. John Wiley & Sons, New York

    Google Scholar 

  • Prokopy RJ (1980) Epideictic pheromones influencing spacing patterns of phytophagous insects In: DA Nordlund, RL Jones, WJ Lewis (eds) Semiochemicals: Their Role in Pest Control. Wiley Press, New York

    Google Scholar 

  • Rauscher MD (1979) Larval habitat suitability and oviposition preference in three related butterflies. Ecology 60:503–511

    Google Scholar 

  • Renwick JAA, Radke CD (1980) An oviposition deterrent associated with the frass from feeding larvae of the cabbage looper, Trichoplusia ni (Lepidoptera: Noctuidae). Environ Ent 9:318–320

    Google Scholar 

  • Ricklefs RE (1973) Ecology. Chiron Press, Portland

    Google Scholar 

  • Rothschild M, Schoonhoven LM (1977) Assessment of egg load by Pieris brassicae (Lepidoptera, Pieridae). Nature (Lond) 266:352–355

    Google Scholar 

  • White GG (1981) Current status of prickly pear control by Cactoblastis cactorum in Queensland. In E Del Fosse (ed) Proc V Int Symp Biol Cont Weeds, Canberra

  • Wicklund C (1975) The evolutionary relationship between adult oviposition preferences and larval host plant range in Papilio machaon L. Oecologia (Berl) 18:185–197

    Google Scholar 

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This paper is dedicated to the memory of our friend Mike Sabath.

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Myers, J.H., Monro, J. & Murray, N. Egg clumping, host plant selection and population regulation in Cactoblastis cactorum (Lepidoptera). Oecologia 51, 7–13 (1981). https://doi.org/10.1007/BF00344644

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  • DOI: https://doi.org/10.1007/BF00344644

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