Skip to main content
Log in

The alkaloidal responses of wild tobacco to real and simulated herbivory

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

Summary

I compared the induced alkaloidal response in undamaged leaves of plants subjected to herbivory by the larvae of Manduca sexta and to different simulations of this herbivory; all herbivory treatments removed similar amounts of leaf mass. Although larval feeding induced a significant increase (2.2x) in alkaloid concentrations compared to undamaged plants, the alkaloid responses to larval feeding were significantly lower than the responses to an herbivory simulation (4x controls) which involved removing the same amount of leaf area from the same positions on the leaf, over a similar time period. Moreover, another herbivory simulation, identical in amount of leaf mass removed and duration of damage to the larval feeding, but without regard to spatial array of leaf damage, resulted in an alkaloidal response (5.5x controls) higher still than the previous herbivory simulation. In a second experiment the importance of leaf vein damage on the induced alkaloidal response was examined. Here, leaf removal that involved cutting leaf tissues from between secondary veins before removing the midrib, resulted in alkaloidal responses that were significantly lower (1.7x controls) than responses from leaf removal that involved cutting both veins and midribs along with the intervein tissues (2.6x controls). Vein damage alone did not produce a significant response. These results indicate that herbivory is difficult to simulate: that how a leaf is damaged can be as important as the magnitude of leaf damage in determining a plant's response to damage.

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

  • Baldwin IT (1988a) Damage-induced alkaloids in tobacco: potbound plants are not inducible. J Chem Ecol 14:1113–1120

    Google Scholar 

  • Baldwin IT (1988b) Short-term damage induced alkaloids protect plants. Oecologia 75:367–370

    Google Scholar 

  • Baldwin IT (1988c) The mechanism of damage-induced alkaloids in wild tobacco. J Chem Ecol (in press)

  • Baldwin IT, Schultz JC (1983) Rapid changes in tree leaf chemistry induced by damage: evidence for communication between plants. Science 221:277–279

    Google Scholar 

  • Capinera JL, Roltsch WJ (1980) Response of wheat seedlings to actual and simulated migratory grasshopper defoliation. J Econ Entomol 73:258–261

    Google Scholar 

  • Caswell H, Reed FC (1975) Indigestibility of C4 bundle sheath cells by the grasshopper Melanoplus confusus. Ann Entomol Soc Am 68:686–688

    Google Scholar 

  • Caswell H, Reed FC (1976) Plant herbivory interactions. The indigestibility of C4 bundle sheath cells by grasshoppers. Oecologia (Berlin) 26:151–156

    Google Scholar 

  • Chew V (1977) Comparison among treatment means in an analysis of variance. USDA Publication ARS/H

  • Hagen RH, Chabot JF (1986) Leaf anatomy of maples (Acer) and host use by Lepidoptera larvae. Oikos 47:335–345

    Google Scholar 

  • Harvell CD (1986) The ecology and evolution of inducible defenses in a marine bryozoan: cues, costs and consequences. Am Nat 128:810–823

    Google Scholar 

  • Haukioja E, Neuvonen S (1985) Induced long-term resistance of birch foliage against defoliators: defense or incidental? Ecology 66:1303–1308

    Google Scholar 

  • Heinrich B (1971) The effect of leaf geometry on the feeding behavior of the caterpillar of Manduca sexta (Sphingidae). Anim Behav 19:119–127

    Google Scholar 

  • Hori K (1976) Plant growth-regulating factor in the salivary gland of several heteropterous insects. Comp Biochem Physiol 53B:435–438

    Google Scholar 

  • McFadden MW (1968) Observations on feeding and movement of tobacco hornworm larvae. J Econ Entomol 61:352–356

    Google Scholar 

  • Madden AH (1945) Biology of the tobacco hornworm in the southern cigar-tobacco district. U.S.D.A. Tech Bull 896

  • Miles PW, Lloyd J (1967) Synthesis of a plant hormone by the salivary apparatus of plant-sucking Hemiptera. Nature 213:801–802

    Google Scholar 

  • Rosa N (1973) Sampling of NIcotiana tabacum leaf lamina to surmount the problem of non-uniform distribution of total alkaloids. Can J Bot 51:289–291

    Google Scholar 

  • Rossiter M, Schultz JC, Baldwin IT (1988) Relationships among defoliators, red oak phenolics, and gypsy moth growth and reproduction. Ecology 69:267–277

    Google Scholar 

  • Ryan CA, Green TR (1974) Proteinase inhibitors in natural plant protection. Rec Adv Phytochem 18:123–140

    Google Scholar 

  • Ryan TA Jr, Joiner BL, Ryan BF (1982) Minitab reference manual. Minitab Inc., State College, PA

    Google Scholar 

  • Ryan CA, Bishop PD, Graham JS, Broadway RM, Duffey SS (1986) Plant and fungal cell wall fragments activate expression of proteinase inhibitor genes for plant defense. J Chem Ecol 12:1025–1036

    Google Scholar 

  • Zeringue HJ (1987) Changes in cotton leaf chemistry induced by volatile elicitors. Phytochemistry 26:1357–1360

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Baldwin, I.T. The alkaloidal responses of wild tobacco to real and simulated herbivory. Oecologia 77, 378–381 (1988). https://doi.org/10.1007/BF00378046

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00378046

Key words

Navigation