Skip to main content
Log in

The fast mandible strike in the trap-jaw ant Odontomachus

II. Motor control

  • Original Paper
  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Abstract

Ants of the ponerine genus Odontomachus employ a trap jaw mechanism for prey catching or defense. The mandible strike is released within less than 10 ms upon stimulation of particular mechanosensory trigger hairs. It is based on the storage of mechanical energy produced by the large but slow mandible closer muscle which cocks the mandible several seconds in advance of the strike.

The strike is released from the catch by a small trigger muscle composed of tubular fibers. It features fast potentials and highly synchronized activation of all its muscle fibers only a few milliseconds in advance of the strike. The trigger muscle is supplied by two unusually large motor neurons that are enclosed in a glial sheath. The trap jaw action is thus controlled by a system composed of 2 giant sensory and 2 giant motor neurons on either side. The giant neurons are most likely monosynaptically coupled. The large axon diameter and the synaptic coupling result in high conduction velocity which underlies the very fast mandible reflex. The reflex activity is modulated by antennal and other sensory input probably converging onto the large dendritic trees of the trigger motor neurons.

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

Abbreviations

ejps :

excitatory junctional potential

SOG :

suboesophageal ganglion

References

  • Barth R (1960) Ueber den Bewegungsmechanismus der Mandibeln von Odontomachus chelifer Latr. (Hymenopt., Formicidae). An Acad Brasil Ciencias 32: 373–384

    Google Scholar 

  • Bullock TH, Horridge GA (1965) Structure and function in the nervous system of invertebrates. W.H. Freeman and Co., San Francisco

    Google Scholar 

  • Carlin NF, Gladstein DS (1989) The “bouncer” defense of Odontomachus ruginodis and other odontomachine ants (Hymenoptera: Formicidae). Psyche 96: 1–19

    Google Scholar 

  • Dejean A, Bashingwa E (1985) La predation chez Odontomachus troglodytes Santschi (Formicidae — Ponerinae). Insecte Soc 32: 23–42

    Google Scholar 

  • Eaton RC (1984) Neural mechanisms of startle behavior. Plenum, New York London

    Google Scholar 

  • Faber DS, Korn H (1978) Neurobiology of the Mauthner cell. Raven, New York

    Google Scholar 

  • Gronenberg W (1995) The fast mandible strike in the trap-jaw ant Odontomachus. I. Temporal properties and morphological characteristics. J Comp Physiol A 176: 391–398

    Google Scholar 

  • Gronenberg W, Peeters C (1993) Central projections of the sensory hairs on the gemma of the ant Diacamma: substrate for behavioral modulation? Cell Tissue Res 273: 401–415

    Google Scholar 

  • Gronenberg W, Tautz J (1994) The sensory basis for the trap-jaw mechanism in the ant Odontomachus bauri. J Comp Physiol A 174: 49–60

    Google Scholar 

  • Gronenberg W, Tautz J, Hölldobler B (1993) Fast trap jaws and giant neurons in the ant Odontomachus. Science 262: 561–563

    Google Scholar 

  • Günther J (1976) Impulse conduction in the myelinated giant fibers of the earthworm. Structure and function of the dorsal nodes in the median giant fiber. J Comp Neurol 168: 505–532

    Google Scholar 

  • Guthrie DM (1980) Neuroethology (an Introduction). Blackwell Scientific Publ. Oxford London Edinburgh Boston Melbourne, pp 53–72

    Google Scholar 

  • Hama K (1959) Some observations on the fine structure of the giant nerve fibers of the earthworm Eisenia foetida. J Biophys Biochem Cytol 6: 61–66

    Google Scholar 

  • Heuser JE, Doggenweiler CF (1966) The fine structural organization of nerve fibers, sheaths, and glial cells in the prawn, Palaemonetes vulgaris. J Cell Biol 30: 382–403

    Google Scholar 

  • Hölldobler B, Wilson EO (1990) The ants. Belknap Press of Harvard University Press, Cambridge Mass

    Google Scholar 

  • Holmes W (1942) The giant myelinated nerve fibers of the prawn. Phil Trans R Soc Lond B 231: 293–311

    Google Scholar 

  • Hoyle G (1975) The neural control of skeletal muscles. In: Usherwood PNR (ed) Insect muscle. Academic Press, London New York San Francisco, pp 501–543

    Google Scholar 

  • Hoyle G (1983) Muscles and their neural control. Wiley, New York

    Google Scholar 

  • Hudspeth AJ, Poo MM, Stuart AE (1977) Passive signal propagation and membrane properties in median photoreceptors of the giant barnacle. J Physiol Lond 272: 25–43

    Google Scholar 

  • Jaffe K, Marcuse M (1983) Nestmate recognition and territorial behaviour in the ant Odontomachus bauri Emery (Formicidae: Ponerinae). Insectes Soc 30: 466–481

    Google Scholar 

  • Josephson RK, Young D (1981) Synchronous and asynchronous muscles in cicadas. J Exp Biol 91: 219–237

    Google Scholar 

  • Kanzaki R, Arbas E, Hildebrand JG (1991) Physiology and morphology of descending neurons in pheromone-processing olfactory pathways in the male moth Manduca sexta. J Comp Physiol A 169: 1–14

    Google Scholar 

  • Kao CY, Grundfest H (1957) Postsynaptic electrogenesis in septate giant axons. I. Earthworm median giant axon. J Neurophysiol 20: 553–573

    Google Scholar 

  • Kusano K (1966) Electrical activity and structural correlates of giant nerve fibers in Kuruma shrimp (Penaeus japonicus). J Cell Physiol 68: 361–384

    Google Scholar 

  • Kusano K, La Vail MM (1971) Impulse conduction in the shrimp medullated giant fiber with special reference to the structure of functionally excitable areas. J Comp Neurol 142: 481–494

    Google Scholar 

  • McAlear JH, Milburn NS, Chapman GB (1958) The fine structure of Schwann cells, nodes of Ranvier and Schmidt-Lanterman incisures in the central nervous system of the crab, Cancer irroratus. J Ultrastruct Res 2: 171–176

    Google Scholar 

  • Milde JJ, Strausfeld NJ (1990) Cluster organization and response characteristics of the giant fiber pathwy of the blowfly Calliphora erythrocephala. J Comp Neurol 294: 59–75

    Google Scholar 

  • Nicol JAC (1948) The giant nerve-fibres in the central nervous system of Myxicola (Polychaetae, Sabellidae). Q J Microp Sci 89: 1–45

    Google Scholar 

  • Osborne MP (1975) The ultrastructure of nerve-muscle synapses. In: Usherwood PNR (ed) Insect muscle. Academic Press, London New York San Francisco, pp 151–205

    Google Scholar 

  • Rehder V (1989) Sensory pathways and motor neurons of the proboscis reflex in the suboesophageal ganglion of the honey bee. J Comp Neurol 279: 499–513

    Google Scholar 

  • Rushton WAH (1946) Reflex conduction in the giant fibres of the earthworm. Proc R Soc Lond B 133: 109–120

    Google Scholar 

  • Strausfeld NJ, Bassemir U, Singh RN, Bacon JP (1984) Organizational principles of outputs from dipteran brains. J Insect Physiol 30: 73–93

    Google Scholar 

  • Terakawa S, Hsu K (1991) Ionic currents of the nodal membrane underlying the fastest saltatory conduction in myelinated giant nerve fibers of the shrimp Penaeus japonicus. J Neurobiol 22: 324–352

    Google Scholar 

  • Wheeler WM (1900) A study on some Texan Ponerinae. Biol Bull 2: 1–31

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gronenberg, W. The fast mandible strike in the trap-jaw ant Odontomachus . J Comp Physiol A 176, 399–408 (1995). https://doi.org/10.1007/BF00219065

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00219065

Key words

Navigation