Skip to main content

Three-trophic-level interactions in cattail hybrid zones

Abstract

Plant-herbivore and herbivore-parasitoid wasp interactions were examined in three hybrid zones of the cattails Typha latifolia and T. angustifolia in south-eastern Michigan over a 2-year period. Patterns of resource use by two lepidopteran species of seed-eating herbivores were studied and herbivore densities sustained by the hybrid cattail T. x glauca and its parental species were determined. Densities of the commoner seed-eating lepidopteran, Lymnaecia phragmitella, were found to be highest in seed heads of both parental species and lowest in hybrid seed heads in zones of hybridization, thus supporting the hybrid resistance hypothesis of Fritz et al. (1994). Densities of the second herbivore, Dicymolomia julianalis, on the hybrid were lower than on the parental T. latifolia, but did not differ from the mean of the combined herbivore densities of the two parental species. D. julianalis in cattails appears to fit the additive hypothesis (Fritz et al. 1994). Parasitism of L. phragmitella by four species of parasitoid wasp, Itoplectis conquisitor (Ichneumonidae), Scambus hispae (Ichneumonidae), Macrocentrus delicatus (Braconidae), and Temelucha gracilipes (Ichneumonidae), was studied to determine if rates of parasitization by these natural enemics on the different cattails were similar to the patterns of plant exploitation exhibited by their hosts. Parasitism rates of L. phragmitella were significantly higher in larvae reared on hybrid cattails. This study reveals two different patterns of hybrid utilization by two very similar herbivores. Opposite patterns of plant utilization were found for the parasitoids compared with their host (L. phragmitella) in cattail hybrid zones.

This is a preview of subscription content, access via your institution.

References

  • Abrahamson WG (1989) Plant-animal interactions: an overview. In: Abrahamson WG (ed) Plant-animal interactions. McGraw Hill, New York, pp 1–22

    Google Scholar 

  • Aguilar JM, Boecklen WJ (1992) Patterns of herbivory in Quercus grisea×Q. gambelii species complex. Oikos 64: 498–504

    Google Scholar 

  • Baker HG (1951) Hybridization and natural gene-flow between higher plants. Biol Rev 26: 302–337

    Google Scholar 

  • Barbosa P (1988) Natural enemies and herbivore-plant interactions: influence of plant allelochemics and host specificity. In Barbosa P, Letourneau DK (eds) Novel aspects of insect-plant interactions. Wiley, New York, pp 201–234

    Google Scholar 

  • Bernays EA, Graham M (1988) On the evolution of host specificity in phytophagous arthropods. Ecology 69: 886–892

    Google Scholar 

  • Boecklen WJ, Spellenberg R (1990) Structure of herbivore communities in two oak (Quercus spp.) hybrid zones. Oecologia 58: 92–100

    Google Scholar 

  • Butler HG (1933) Larval parasites of the oriental fruit moth in Roane County, Tennessee. J Econ Entomol 26: 982–987

    Google Scholar 

  • Campbell BC, Duffey SF (1979) Tomatine and parasitic wasps: potential incompatibility of plant antibiosis with biological control. Science 20: 700–702

    Google Scholar 

  • Campbell BC, Duffey SF (1981) Alleviation of a-tomatine induced toxicity to the parasitoid Hyperoster exiguae by photosterols in the diets of the host Heliothis zea. J Chem Ecol 7: 927–946

    Google Scholar 

  • Claassen PW (1921) Typha insects: their ecological relationships. Cornell Univ Agric Exp Sta Mem 47: 459–531

    Google Scholar 

  • Cole AC Jr (1931) Typha insects and their parasites. Entomol News 42: 6–11, 35–39

    Google Scholar 

  • Dasch CE (1979) Ichneumon-flies north of Mexico: 8: Subfamily Cremastinae. Am Entomol Inst Mem 29

  • Drake DW (1981a) Reproductive success of two Eucalyptus hybrid populations. I. Generalized seed output model and comparison of fruit parameters. Aust J Bot 29: 25–35

    Google Scholar 

  • Drake DW (1981b) Reproductive success of two Eucalyptus hybrid populations. II. Comparison of predispersal seed parameters. Aust J Bot 29: 37–48

    Google Scholar 

  • Fassett NC, Calhoun BM (1952) Introgression between Typha latifolia and T. angustifolia. Evolution 6: 367–379

    Google Scholar 

  • Floate KD, Whitham TG (1993) The “hybrid bridge” hypothesis: host shifting via plant hybrid swarms. Am Nat 141: 651–662

    Google Scholar 

  • Floate KD, Kearsley MJC, Whitham TG (1993) Elevated herbivory in plant hybrid zones: Chrysomela confluens, Populus and phenological sinks. Ecology 74: 2056–2065

    Google Scholar 

  • Fox LR (1981) Detense and dynamics in plant/herbivore systems. Am Zool 21: 853–864

    Google Scholar 

  • Fox LR (1988) Diffuse coevolution within complex communities. Ecology 69: 906–907

    Google Scholar 

  • Fox LR, Eisenbach J (1992) Contrary choices: possible exploitation of enemy-free space by herbivorous insects in cultivated vs. wild crucifers. Oecologia 89: 574–579

    Google Scholar 

  • Fox LR, Morrow P (1981) Specialization: species property or local phenomenon? Science 211: 887–893

    Google Scholar 

  • Fox LR, Letourneau DK, Eisenbach J, Van Nouhuys S (1990) Parasitism rates and sex ratios of a parasitoid wasp: effects of herbivore and plant quality. Oecologia 83: 414–419

    Google Scholar 

  • Fritz RS, Nichols-Orians CM, Brunsfeld SJ (1994) Interspecific hybridization of plants and resistance to herbivores: hypotheses, genetics, and variable responses in a diverse herbivore community. Oecologia 97: 106–117

    Google Scholar 

  • Grant V (1981) Plant speciation, 2nd edn. Columbia University Press, New York

    Google Scholar 

  • Greenblatt JA, Barbosa P (1981) Effects of host's diet on two pupal parasitoids of the gypsy moth: Brachymeria intermedia (Ness) and Coccygominus turionellae (L). J Appl Ecol 18: 1–10

    Google Scholar 

  • Heiser CB Jr (1949) Natural hybridization with particular reference to introgression. Bot Rev 15: 645–687

    Google Scholar 

  • Hotchkiss N, Dozier HL (1949) Taxonomy and distribution of N. American cat-tails. Am Midland Nat 41: 237–254

    Google Scholar 

  • Jaynes HA, Drooz AT (1952) The importance of parasites in the spruce budworm infestations in New York and Maine. J Econ Entomol 45: 1057–1061

    Google Scholar 

  • Lawton JH (1986) The effects of parasitoids on phytophagous insect communities. In: Waage J, Greathead D (eds) Insect parasitoids. 13th Symposium of the Royal Entomological Society, London. Academic Press, London, pp 265–289

    Google Scholar 

  • Manley AM, Fowler DP (1969) Spruce budworm defoliation in relation to introgression in red and black spruce. For Sci 15: 365–366

    Google Scholar 

  • Moorehead JR, Taper MI, Case TJ (1993) Utilization of hybrid oak hosts by a monophagous gall wasp: how little host character is sufficient? Oecologia 95: 3385–3392

    Google Scholar 

  • Morrow PA, Whitham TG, Potts BM, Ladiges P, Ashton DH, Williams JB (1994) Gall-forming insects concentrate on hybrid phenotypes of Eucalyptus hosts. In: Price PW, Mattson WJ, Baranchikov YN (eds) The ecology and evolution of gall-forming insects (GTR NC-174). USDA Forest Service, North Central Forest Exp. STA., pp 121–134

  • Nordlund DA, Lewis WJ, Gross HR Jr (1981) Elucidation and employment of semiochemicals in the manipulation of entomaphagous insects. In: Mitchell ER (ed) Management of insect pests with semiochemicals: concepts and practice. Plenum, New York, pp 463–475

    Google Scholar 

  • Paige KN, Capman WC (1993) The effects of host-plant genotype, hybridization and environment on gall aphid attack and survival in cottonwood: the importance of genetic studies and the utility of RFLPS. Evolution 47: 36–45

    Google Scholar 

  • Penko JM (1985) Ecological studies of Typha in Minnesota: Typha-insect interactions, and the productivity of floating stands. M.S. Thesis, University of Minnesota, Minneapolis

  • Penko JM, Pratt DC (1987) Insect herbivory in Minnesota Typha stands. J Freshwater Ecol 4: 235–244

    Google Scholar 

  • Price PW (1986) Ecological aspects of host plant resistance and biological control: interactions among three trophic levels. In: Boethal DJ, Eikenbarry RD (eds) Interactions of plant resistance and parasitoids and predators of insects. Wiley, New York, pp 11–30

    Google Scholar 

  • Price PW, Bouton CE, Gross P, McPherson BA, Thompson JN, Weis AE (1980) Influence of plants on interactions between insect herbivores and natural enemies. Ann Rev Ecol Syst 11: 41–65

    Google Scholar 

  • Rieseberg LH, Wendel JF (1993) Introgression and its consequences in plants. In: Harrison RG (ed) Hybrid zones and the evolutionary process. Oxford University Press, New York, pp 70–109

    Google Scholar 

  • Sharitz RR, Wineriter SA, Smith MH, Liu EH (1980) Comparisons of isozymes among Typha spp. in the eastern USA. Am J Bot 67: 1297–1303

    Google Scholar 

  • Shay JM (1984) Vegetation dynamics in the Delta Marsh, Manitoba. In: Clamby GK, Pemble RH (eds) Proceedings of the 9th North American prairie conference. Tri-university Press, Moorehead, Minnesota, pp 65–70

    Google Scholar 

  • Shepard M, Dahlman DL (1988) Plant induced stresses as factors in natural enemy efficacy. In: Heinrichs EA (ed) Plant stressinsect interactions. Wiley, New York, pp 363–379

    Google Scholar 

  • Smith SG (1967) Experimental and natural hybrids in North American Typha (Typhaceae). Am Midland Nat 78: 257–287

    Google Scholar 

  • Smith SG (1987) Typha: Its taxonomy and the ecological significances of hybrids. Arch Hydrobiol Beih 27: 129–138

    Google Scholar 

  • Sokal RR, Rohlf J (1969) Biometry. Freeman, San Francisco

    Google Scholar 

  • Stace CA (1987) Hybridization and the plant species. In: Urbanska KM (ed) Differentiation patterns in higher plants. Academic Press, New York, pp 115–127

    Google Scholar 

  • Stebbins GL (1950) Variation and evolution in plants. Columbia University Press, New York

    Google Scholar 

  • Stebbins GL (1959) The role of hybridization in evolution. Proc Am Philos Soc 103: 231–251

    Google Scholar 

  • Valk AG van der, Davis CB (1980) The impact of a natural drawdown on the growth of four emergent species in a prairie glacial marsh. Aquat Bot 9: 301–322

    Google Scholar 

  • Vinson B, Barbosa P (1988) Interrelationships of nutritional ecology of parasitoids. In: Slansky F, Rodriguez JG (eds) Nutritional ecology of insects, mites, spiders and related invertebrates. Wiley, New York, pp 673–686

    Google Scholar 

  • Wendell JF, Stewart JM, Rettig JH (1991) Molecular evidence for homoploid reticulate evolution among Australian species of Gossypium. Evolution 45: 694–711

    Google Scholar 

  • Whilham TG (1989) Plant hybrid zones as sinks for pests. Science 244: 1490–1493

    Google Scholar 

  • Wilkes A, Coppel HC, Mathers WG (1948) Notes on the insect parasites of the spruce budworm Choristoneura fumiferana (Clem.) in British Columbia. Can Entomol 80: 138–155

    Google Scholar 

  • Williams HJ, Elzen GW, Vinson SB (1988) Parasitoid-host-plant interactions, emphasizing cotton (Gossypium) In: Barbosa P Letourneau DK (eds) Novel aspects of insect-plant interactions. Wiley, New York, pp 94–113

    Google Scholar 

Download references

Author information

Affiliations

Authors

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Eisenbach, J. Three-trophic-level interactions in cattail hybrid zones. Oecologia 105, 258–265 (1996). https://doi.org/10.1007/BF00328555

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00328555

Key words

  • Plant hybridization
  • Three-trophic-level interactions
  • Herbivores
  • Parasitoids
  • Typha