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How the Venus flytrap snaps

Abstract

The rapid closure of the Venus flytrap (Dionaea muscipula) leaf in about 100 ms is one of the fastest movements in the plant kingdom. This led Darwin to describe the plant as “one of the most wonderful in the world”1. The trap closure is initiated by the mechanical stimulation of trigger hairs. Previous studies2,3,4,5,6,7 have focused on the biochemical response of the trigger hairs to stimuli and quantified the propagation of action potentials in the leaves. Here we complement these studies by considering the post-stimulation mechanical aspects of Venus flytrap closure. Using high-speed video imaging, non-invasive microscopy techniques and a simple theoretical model, we show that the fast closure of the trap results from a snap-buckling instability, the onset of which is controlled actively by the plant. Our study identifies an ingenious solution to scaling up movements in non-muscular engines and provides a general framework for understanding nastic motion in plants.

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Figure 1: Dynamics of Venus flytrap closure.
Figure 2: Strain field and natural curvature.
Figure 3: Smooth–snapping transition in leaf closure.
Figure 4: Speed of closure and delay between triggering and snapping.

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References

  1. Darwin, C. Insectivorous Plants (Murray, London, 1875)

    Google Scholar 

  2. Burdon-Sanderson, J. On the electromotive properties of the leaf of dionaea in the excited and unexcited states. Phil. Trans. R. Soc. Lond. 173, 1–55 (1882)

    Article  ADS  Google Scholar 

  3. Stuhlman, O. Jr & Darder, E. B. The action potentials obtained from Venus's-flytrap. Science 111, 491–492 (1950)

    Article  ADS  Google Scholar 

  4. Hodick, D. & Sievers, A. The action potential of Dionaea muscipula Ellis. Planta 174, 8–18 (1988)

    Article  CAS  Google Scholar 

  5. Hodick, D. & Sievers, A. On the mechanism of trap closure of Venus flytrap (Dionaea muscipula Ellis). Planta 179, 32–42 (1989)

    Article  CAS  Google Scholar 

  6. Sibaoka, T. Physiology of rapid movements in higher plants. Annu. Rev. Plant Physiol. 20, 165–184 (1969)

    Article  CAS  Google Scholar 

  7. Juniper, B. E., Robins, R. J. & Joel, D. M. The Carnivorous Plants (Academic, London, 1989)

    Google Scholar 

  8. Williams, S. E. & Bennet, A. B. Leaf closure in the Venus flytrap: an acid growth response. Science 218, 1120–1122 (1982)

    Article  ADS  CAS  Google Scholar 

  9. Stuhlman, O. A physical analysis of the opening and closing movements of the lobes of Venus' flytrap. Bull. Torrey Bot. Club 7, 22–44 (1948)

    Article  Google Scholar 

  10. Ashida, J. Studies on leaf movement of Aldrovanda vesiculosa . Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B 9, 141–244 (1934)

    Google Scholar 

  11. Morillon, R., Liénard, D., Chrispeels, M. J. & Lassalles, J.-P. Rapid movements of plants organs require solute-water cotransporters or contractile proteins. Plant Physiol. 127, 720–723 (2001)

    Article  CAS  Google Scholar 

  12. Brown, W. H. The mechanism of movement and duration of the effect of stimulation in the leaves of dionaea. Am. J. Bot. 3, 68–90 (1916)

    Article  Google Scholar 

  13. Hill, B. S. & Findlay, G. P. The power of movement in plants: the role of osmotic machines. Q. Rev. Biophys. 14, 173–222 (1981)

    Article  CAS  Google Scholar 

  14. Love, A. E. H. A Treatise on the Mathematical Theory of Elasticity 4th edn (Dover, New York, 1944)

    MATH  Google Scholar 

  15. Biot, M. A. General theory of three-dimensional consolidation. J. Appl. Phys. 12, 155–165 (1941)

    Article  ADS  Google Scholar 

  16. Skotheim, J. M. & Mahadevan, L. Dynamics of poroelastic filaments. Proc. R. Soc. Lond. A 460, 1995–2020 (2004)

    Article  ADS  MathSciNet  Google Scholar 

  17. Frensch, J. & Steudle, E. Axial and radial hydraulic resistance to roots of maize (Zea mays L.). Plant Physiol. 91, 719–726 (1989)

    Article  CAS  Google Scholar 

  18. Dumais, J. & Kwiatkowska, D. Analysis of surface growth in shoot apices. Plant J. 31, 229–241 (2002)

    Article  Google Scholar 

  19. Green, P. B., Havelange, A. & Bernier, G. Floral morphogenesis in Anagallis: Scanning-electron-micrograph sequences from individual growing meristems before, during, and after the transition to flowering. Planta 185, 502–512 (1991)

    Article  CAS  Google Scholar 

  20. Mansfield, E. H. The Bending and Stretching of Plates 2nd edn (Cambridge Univ. Press, Cambridge, 1989)

    Book  Google Scholar 

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Acknowledgements

We thank F. Shindler for the illustrations in Fig. 2. We acknowledge support via the Norwegian Research Council (J.M.S.) and the Schlumberger Chair Fund (L.M.) at Cambridge University, where this work was begun and primarily done.

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Correspondence to L. Mahadevan.

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The authors declare that they have no competing financial interests.

Supplementary information

Supplementary Video

Kinematic measurements of snapping were carried out on videos filmed at 400 frames s-1. Here we show a representative video of leaf closure filmed at the slightly lower speed of 125 frames s-1 and played back at 30 frames s-1. (MOV 5597 kb)

Supplementary Methods

This section includes (a) details of the strain-field measurement technique, (b) experiments and results regarding the response of the leaf tissue to impulsive and step loads, (c) details of our poroelastic model for the dynamics of leaf closure, and (d) a summary of our notation. (DOC 68 kb)

Supplementary Figure 1

This figure presents typical measurements of the local strain field associated with leaf closure, determined using the replica technique. (PDF 2319 kb)

Supplementary Figure 2

This figure shows the response of a strip of the closed leaf to impulse and step loads. The results are consistent with the simple estimate of the inertial and relaxation times in the main text of the paper. (PDF 408 kb)

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Forterre, Y., Skotheim, J., Dumais, J. et al. How the Venus flytrap snaps. Nature 433, 421–425 (2005). https://doi.org/10.1038/nature03185

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