Skip to main content
Log in

The iridoid glycoside, catalpol, as a deterrent to the predatorCamponotus floridanus (Formicidae)

  • Research papers
  • Published:
CHEMOECOLOGY Aims and scope Submit manuscript

Summary

We investigated the role of the iridoid glycoside, catalpol, as a deterrent to the predator,Camponotus floridanus. Four laboratory colonies of this ant were offered buckeye caterpillars (Junonia coenia: Nymphalidae) raised on diets with and without catalpol. The same colonies were offered sugar-water solutions containing varying concentrations of catalpol, in both no-choice and choice tests. Regardless of diet, buckeye caterpillars appeared to be morphologically protected from predation by the ants, possibly because of their large spines or tough cuticle. However, buckeyes raised on diets with catalpol had high concentrations of catalpol in their hemolymph; extracts of this high-catalpol hemolymph proved to be an effective deterrent to the ants. When starved ants were not given the choice of food items, they were more likely to consume sucrose solutions that contained 5 mg catalpol/ml or 10 mg catalpol/ml than they were to consume solutions with 20 mg catalpol/ml. When they were given a choice of sugar solution or a sugar solution containing catalpol, the ants avoided solutions with catalpol at any of these concentrations. Ant colony responses to catalpol in sucrose solutions varied considerably over time and among colonies.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bernays EA (1988) Host specificity in phytophagous insects: selection pressure from generalist predators. Entomol exp appl 49:131–140

    Article  Google Scholar 

  • Bobbitt JM, Segebarth DP (1969) Iridoid glycosides and similar substances. Pp 1–145in Taylor WI, Battersby AR (eds) Cyclopentanoid Terpene Derivatives. New York: Academic Press

    Google Scholar 

  • Bowers MD (1980) Unpalatability as a defense strategy ofEuphydryas phaeton. Evolution 34:586–600

    Google Scholar 

  • Bowers MD (1984) Iridoid glycosides and hostplant specificity in larvae of the buckeye butterfly,Junoni coenia (Nymphalidae). J Chem Ecol 10:1567–1577

    Article  Google Scholar 

  • Bowers MD (1991) Iridoid glycosides. Pp 297–325in Rosenthal G, Berenbaum M (eds) Herbivores: Their Interactions with Secondary Plant Metabolites. 2nd ed. Volume I: The Chemical Participants. Orlando FL: Academic Press

    Google Scholar 

  • Bowers MD, Collinge SK (1992) Fate of iridoid glycosides in different life stages of the buckeye,Junonia coenia (Lepidoptera: Nymphalidae). J Chem Ecol 18:317–831

    Google Scholar 

  • Bowers MD, Puttick GM (1989) Iridoid glycosides and insect feeding preferences: gypsy moths (Lymantria dispar, Lymantriidae) and buckeyes (Junonia coenia, Nymphalidae). Ecol Entomol 14:247–256

    Google Scholar 

  • Bowers MD, Stamp NE (1992) Chemical variation within and between individuals ofPlantago lanceolata (Plantaginaceae). J Chem Ecol 18:985–995

    Article  Google Scholar 

  • Brower LP (1984) Chemical defense in butterflies. Pp 109–134in Vane-Wright RI, Ackery PR (eds) The Biology of Butterflies. Symp Royal Entomol Soc 11. New York: Academic Press

    Google Scholar 

  • Brower LP, Brower JVZ, Corvino JM (1967) Plant poisons in a terrestrial food chain. Proc Nat Acad Sci 57:893–898

    PubMed  Google Scholar 

  • Campbell RW, Torgersen TR, Srivastava N (1983) A suggested role for predaceous birds and ants in the population dynamics of the western spruce budworm. Forest Science 29:779–790

    Google Scholar 

  • Carlin NF, Schwartz PH (1989) Pre-imaginal experience and nestmate brood recognition in the carpenter ant,Camponotus floridanus. Anim Behav 38:89–95

    Google Scholar 

  • Carney WP (1970) Laboratory maintenance of carpenter ants. Ann Entomol Soc Am 63:333–334

    Google Scholar 

  • Cott HB (1940) Adaptive Coloration in Animals. New York: Oxford University Press

    Google Scholar 

  • Dejean A (1988) Prey capture byCamponotus maculatus (Formicidae — Formicinae). Biol Behav 13:97–115

    Google Scholar 

  • Dempster JP (1984) The natural enemies of butterflies. Pp 97–104in Vane-Wright RI, Ackery PR (eds) The Biology of Butterflies. Symp Royal Entomol Soc 11. New York: Academic Press

    Google Scholar 

  • Duff R, Bacon J, Mucndie C, Farmer V, Russell J, Forrester J, Forrester A (1965) Catalpol and methylcatalpol: naturally occurring glycosides inPlantago andBuddleia species. Biochem J 96:1–5

    PubMed  Google Scholar 

  • Edmunds M (1974) Defence in Animals. GB-Essex: Longman

    Google Scholar 

  • Ford EB (1945) Butterflies. London: Collins

    Google Scholar 

  • Gardner DR, Stermitz FR (1988) Hostplant utilization and iridoid glycoside sequestration byEuphydryas anicia individuals and populations. J Chem Ecol 15:2147–2168

    Article  Google Scholar 

  • Inouye H (1991) Iridoids. Pp 99–143in Charlwood BV, Banthorpe DV (eds) Methods in Plant Biochemistry. Vol 7: Terpenoids. San Diego: Academic Press

    Google Scholar 

  • Jenson SR (1991) Plant iridoids, their biosynthesis and distribution in angiosperms. Pp 133–158in Harborne JB, Tomas-Barberan FA (eds) Ecological Chemistry and Biochemistry of Plant Terpenoids. Oxford: Clarenden Press

    Google Scholar 

  • Lanza J (1991) Response of fire ants (Formicidae:Solenopsis invicta andS. geminata) to artificial nectars with amino acids. Ecol Entomol 16:203–210

    Google Scholar 

  • Mason RR, Trogersen TR (1983) Mortality of larvae in stocked cohorts of the douglas-fir tussock moth,Orgyia pseudotsugata (Lepidoptera: Lymantriidae). Can Entomol 115:1119–1127

    Google Scholar 

  • Merck Index, Tenth Edition (1983) Windholz M, Budavari S, Blumetti RF, Otterbein ES (eds). New Jersey: Merck & Co

  • Morris RF (1972) Predation by wasps, birds, and mammals onHyphantria cunea. Can Entomol 104:1581–1591

    Google Scholar 

  • Nonacs P (1991) Less growth with more food: how insect-prey availability changes colony demographics in the ant,Camponotus floridanus. J Insect Physiol 37:891–898

    Article  Google Scholar 

  • Peterson CH, Renaud PE (1989) Analysis of feeding preference experiments. Oecologia 80:82–86

    Article  Google Scholar 

  • Puttick GM, Bowers MD (1988) Effect of quantitative variation in allelochemicals on a generalist insect: iridoid glycosides and the Southern armyworm. J Chem Ecol 14:335–351

    Article  Google Scholar 

  • Rothschild M (1985) British aposematic Lepidoptera. Pp 9–62in Heath J, Emmet AM (eds) The Moths and Butterflies of Great Britain and Ireland. GB-Essex: Harley Books

    Google Scholar 

  • Stamp NE, Bowers MD (1988) Direct and indirect effects of predatory wasps (Polistes sp: Vespidae) on gregarious caterpillars (Hemileuca lucina: Saturniidae). Oecologia 75:619–624

    Article  Google Scholar 

  • Steward VB, Smith KG, Stephen FM (1988) Predation by wasps on lepidopteran larvae in an Ozark forest canopy. Ecol Entomol 13:81–86

    Google Scholar 

  • Youngs LC (1983) Predaceous ants in biological control of insect pests of a North American forest. Bull Entomol Soc Am 29: 47–50

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

de la Fuente, MA., Dyer, L.A. & Bowers, M.D. The iridoid glycoside, catalpol, as a deterrent to the predatorCamponotus floridanus (Formicidae). Chemoecology 5, 13–18 (1994). https://doi.org/10.1007/BF01259968

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01259968

Key words

Navigation