Skip to main content
Log in

Facilitative interactions between two lepidopteran herbivores of Asimina

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Insect herbivores that require young foliage for successful larval development are often restricted to a single generation during a year by the scarcity of suitable food over most of the growing season. The major specialist herbivore attacking shrubs in the genus Asimina in Florida, Eurytides marcellus, requires young foliage for successful larval development. Field manipulations were used to investigate the role of the young foliage produced by Asimina in response to defoliation by the late-season feeder Omphalocera munroei, a second specialist herbivore of Asimina in Florida, in maintaining Eurytides populations during the summer months when young foliage is otherwise scarce. Defoliation by Omphalocera proved to be the major inducer of young growth during the summer because Omphalocera defoliated Asimina shrubs so frequently and severely. When compared to young leaves produced in the absence of damage, the teaves produced by Asimina in response to defoliation were equally as suitable as food for Eurytides larvae and as acceptable as oviposition sites by Eurytides females. The availability of young foliage in an Asimina population was correlated with the size of the associated Eurytides population. The combination of regular, severe defoliation by Omphalocera and lack of a defensive response to damage by Asimina lead to a positive affect of Omphalocera on Eurytides population size, and may be central to other facilitative interactions between herbivores as well.

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

  • Auerbach M, Simberloff D (1984) Responses of leaf miners to atypical leaf production patterns. Ecol Entomol 9:361–376

    Google Scholar 

  • Carroll CR, Hoffman CA (1980) Chemical feeding deterrent mobilized in response to insect herbivory and counteradaptation by Epilachna tridecemnotata. Science 209:414–416

    Google Scholar 

  • Christensen NL (1981) Fire regimes in southeastern ecosystems. In: Mooney HA, Bonnicksen TM, Christensen NL, Lotan JE, Reiners WA (eds) Fire regimes and ecosystem properties. U S Forest Serv Tech Rep WO-26, pp 112–136

  • Cole LC (1954) The population consequences of life history phenomena. Quart Rev Biol 29:103–137

    Google Scholar 

  • Coley PD (1983) Herbivory and defensive characteristics of tree species in a lowland tropical forest. Ecol Monogr 53:209–233

    Google Scholar 

  • Crawley MJ, Nachapong M (1984) Facultative defenses and specialist herbivores? Cinnabar moth (Tyria jacobaeae) on the regrowth foliage of ragwort (Senecio jacobaea). Ecol Entomol 9:389–393

    Google Scholar 

  • Damman H (1986a) The osmaterial glands of the swallowtail butterfly Eurytides marcellus as a defence against natural enemies. Ecol Entomol 11:261–265

    Google Scholar 

  • Damman H (1986b) Effects of seasonal changes in leaf quality and abundance of natural enemies on the insect herbivores of pawpaws. Ph D Thesis, Cornell University

  • Dixon AFG (1970) Quality and availability of food for a sycamore aphid population. In: Watson A (ed) Animal populations in relation to their food resources. Blackwell Scientific, Oxford, pp 271–282

    Google Scholar 

  • Faeth SH (1986) Indirect interactions between temporally separated herbivores mediated by the host plant. Ecology 67:479–494

    Google Scholar 

  • Faeth SH, Mopper S, Simberloff D (1981) Abundances and diversity of leaf-mining insects on three oak host species: effects of host-plant phenology and nitrogen content of leaves. Oikos 37:238–251

    Google Scholar 

  • Feeny P (1970) Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51:565–581

    Google Scholar 

  • Fowler SV, Lawton JH (1985) Rapidly induced defenses and talking trees: the devil's advocate position. Am Nat 126:181–195

    Google Scholar 

  • Futuyma DJ, Wasserman SS (1980) Resource concentration and herbivory in oak forests. Science 201:920–922

    Google Scholar 

  • Hairston NG, Smith FE, Slobodkin LB (1960) Community structure, population control, and competition. Am Nat 94:421–425

    Google Scholar 

  • Harrison S, Karban R (1986) Effects of an early-season folivorous moth on the success of a late-season species, mediated by a change in the quality of the shared host, Lupinus arboreus Sims. Oecologia 69:354–359

    Google Scholar 

  • Haukioja E, Niemelä P (1979) Birch leaves as a resource for herbivores: seasonal occurrence of increased resistance in foliage after mechanical damage of adjacent leaves. Oecologia 39:151–159

    Google Scholar 

  • Heichel GH, Turner NC (1976) Phenology and leaf growth of defoliated hardwood trees. In: Anderson JF, Kaya HK (eds) Perspectives in forest entomology. Academic Press, New York, pp 31–40

    Google Scholar 

  • Heinrich B (1979) Foraging strategies of caterpillars. Oecologia 42:325–337

    Google Scholar 

  • Hodson AC (1981) The response of aspen (Populus tremuloides) to artificial defoliation. Great Lakes Entomol 14:167–169

    Google Scholar 

  • Hough JA, Pimentel D (1978) Influences of host foliage on development, survival, and fecundity of the gypsy moth. Environ Entomol 7:97–102

    Google Scholar 

  • Jones EW (1959) Biological flora of the British Isles: Quercus L. J Ecol 47:169–222

    Google Scholar 

  • Kalisz PJ, Stone EL (1984) The longleaf pine islands of the Ocala National Forest, Florida: a soil study. Ecology 65:1743–1754

    Google Scholar 

  • Kral R (1960) A revision of Asimina and Deeringothamnus (Annonaceae). Brittonia 12:233–278

    Google Scholar 

  • Lawton JH, Strong DR (1981) Community patterns and competition in folivorous insects. Am Nat 118:317–338

    Google Scholar 

  • Lowman MD (1982a) Effects of different rates and methods of leaf area removal on rain forest seedlings of coachwood (Ceratopetalum apetalum). Austral J Bot 30:477–483

    Google Scholar 

  • Lowman MD (1982b) Seasonal variation in insect abundance among three Australian rain forests, with particular reference to phytophagous types. Austral J Ecol 7:353–361

    Google Scholar 

  • Macauley BJ, Fox LR (1980) Variation in total phenols and condensed tannins in Eucalyptus: leaf phenology and insect grazing. Austral J Zool 5:31–35

    Google Scholar 

  • Nagy M (1979) The effect of Lepidoptera larvae consumption on the leaf production of Quercus petraea (Matt.) Liebl. Acta Bot Acad Sci Hungaricae 27:141–150

    Google Scholar 

  • Niemelä P, Haukioja E (1982) Seasonal patterns in species richness of herbivores: macrolepidoptera larvae on Finnish deciduous trees. Ecol Entomol 7:169–175

    Google Scholar 

  • Opler PA (1974) Biology, ecology, and host specificity of Microlepidoptera associated with Quercus agrifolia (Fagaceae). Univ Calif Publ Entomol 75:1–83

    Google Scholar 

  • Rathcke B (1983) Competition and facilitation among plants for pollination. In: Real L (ed) Pollination biology. Academic Press, New York, pp 305–329

    Google Scholar 

  • Rausher MD (1981) Host plant selection by Battus philenor butterflies: the roles of predation, nutrition, and plant chemistry. Ecol Monogr 51:1–20

    Google Scholar 

  • Reichle DE, Goldstein RA, Van Hook RI, Dodson GJ (1973) Analysis of food consumption in a forest canopy. Ecology 54:1076–1084

    Google Scholar 

  • Rhoades DF (1985) Offensive-defensive interactions between herbivores and plants: their relevance in herbivore population dynamics and ecological theory. Am Nat 125:205–238

    Google Scholar 

  • Rockwood LL (1974) Seasonal changes in the susceptibility of Crescentia alata leaves to the flea beetle, Oedionychus sp. Ecology 55:142–148

    Google Scholar 

  • Schoener TW (1983) Field experiments on interspecific competition. Am Nat 122:240–285

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. WH Freeman & Company, San Francisco

    Google Scholar 

  • South R (1961) The Moths of the British Isles. Frederick Warne & Co, Ltd

  • Springett BP (1978) On the ecological role of insects in Australian eucalypt forests. Austral J Ecol 3:129–139

    Google Scholar 

  • Stearns SC (1976) Life history tactics: a review of the ideas. Quart Rev Biol 51:3–47

    Google Scholar 

  • Washburn JO, Cornell HV (1981) Parasitoids, patches, and phenology: their possible role in the local extinction of a cynipid gall wasp population. Ecology 62:1597–1607

    Google Scholar 

  • Watanabe M (1981) Population dynamics of the swallowtail butterfly, Papilio xuthus L., in a deforested area. Res Popul Ecol 23:74–93

    Google Scholar 

  • Watanabe M (1982) Leaf structure of Zanthoxylum ailanthoides Sieb et Zucc. (Rutales: Rutaceae) affecting the mortality of a swallowtail butterfly, Papilio xuthus L. (Lepidoptera: Papilionidae). Appl Ent Zool 17:151–159

    Google Scholar 

  • Webber HJ (1935) The Florida scrub, a fire-fighting association. Am J Bot 22:344–361

    Google Scholar 

  • West C (1985) Factors underlying the late seasonal appearance of the lepidopteran leaf-mining guild on oak. Ecol Entomol 10:111–120

    Google Scholar 

  • Williams KS, Myers JH (1984) Previous herbivore attack of red alder may improve food quality for fall webworm larvae. Oecologia 63:166–170

    Google Scholar 

  • Wolda H (1978) Seasonal fluctuations in rainfall, food and abundance for tropical insects. J Anim Ecol 47:369–381

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Damman, H. Facilitative interactions between two lepidopteran herbivores of Asimina . Oecologia 78, 214–219 (1989). https://doi.org/10.1007/BF00377158

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00377158

Key words

Navigation