Export citation

Export citation

Choose format for download:

Download Citation
  • Featured in Physics
  • Editors' Suggestion
  • Access by Xinjiang University

Gas flow in plant microfluidic networks controlled by capillary valves

M. Capron*, Ph. Tordjeman, and F. Charru

E. Badel and H. Cochard

  • Université de Toulouse, INPT-CNRS, Institut de Mécanique des Fluides de Toulouse, Allée du Professeur C. Soula, 31400 Toulouse, France

  • INRA, UMR 547 PIAF, 5 chemin de Beaulieu, F-63039 Clermont-Ferrand, France
  • and Clermont Université, Université Blaise Pascal, UMR A547 PIAF, F-63000 Clermont-Ferrand Cedex 2, France

  • *mcapron@imft.fr
  • philippe.tordjeman@imft.fr

Phys. Rev. E 89, 033019 – Published 28 March, 2014

DOI: https://doi.org/10.1103/PhysRevE.89.033019

Abstract

The xylem vessels of trees constitute a model natural microfluidic system. In this work, we have studied the mechanism of air flow in the Populus xylem. The vessel microstructure was characterized by optical microscopy, transmission electronic microscopy (TEM), and atomic force microscopy (AFM) at different length scales. The xylem vessels have length 15 cm and diameter 20μm. Flow from one vessel to the next occurs through 102 pits, which are grouped together at the ends of the vessels. The pits contain a thin, porous pit membrane with a thickness of 310 nm. We have measured the Young's moduli of the vessel wall and of the pits (both water-saturated and after drying) by specific nanoindentation and nanoflexion experiments with AFM. We found that both the dried and water-saturated pit membranes have Young's modulus around 0.4 MPa, in agreement with values obtained by micromolding of pits deformed by an applied pressure difference. Air injection experiments reveal that air flows through the xylem vessels when the differential pressure across a sample is larger than a critical value ΔPc=1.8 MPa. In order to model the air flow rate for ΔPΔPc, we assumed the pit membrane to be a porous medium that is strained by the applied pressure difference. Water menisci in the pit pores play the role of capillary valves, which open at ΔP=ΔPc. From the point of view of the plant physiology, this work presents a basic understanding of the physics of bordered pits.

Focus

Plant Gas Valve under the Microscope

Published 28 March, 2014

Precision measurements of plant microstructures provide new insights into how they prevent gas bubbles from disrupting water flow.

See more in Physics

Article Text

References (33)

  1. M. H. Zimmermann and A. A. Jeje, Can. J. Bot. 59, 1882 (1981).
  2. S. Jansen, B. Choat, and A. Pletsers, Am. J. Bot. 96, 409 (2009).
  3. M. T. Tyree and M. H. Zimmermann, Xylem Structure and the Ascent of Sap, 2nd ed. (Springer-Verlag, Berlin, 2001).
  4. M. T. Tyree and J. S. Sperry, Annu. Rev. Plant Phys. Mol. Biol. 40, 19 (1989).
  5. T. D. Wheeler and A. D. Stroock, Nature 455, 208 (2008).
  6. O. Vincent, P. Marmottant, P. A. Quinto-Su, and C.-D. Ohl, Phys. Rev. Lett. 108, 184502 (2012).
  7. A. D. Stroock, V. V. Pagay, M. A. Zwieniecki, and N. M. Holbrook, Annu. Rev. Fluid Mech. 46, 615 (2014).
  8. A. G. Meyra, V. A. Kuz, and G. J. Zarragoicoechea, Tree Physiol. 27, 1401 (2007).
  9. J. Lee, N. M. Holbrook, and M. A. Zwieniecki, Front. Plant Sci. 3, 55 (2012).
  10. T. C. Pesacreta, L. H. Groom, and T. G. Rials, IAWA J. 26, 397 (2005).
  11. P. G. de Gennes, F. Brochard-Wyart, and D. Quéré, Capillarity and Wetting Phenomena: Drops, Bubbles, Pearls, Waves (Springer, New York, 2004).
  12. G. Binnig, C. F. Quate, and Ch. Gerber, Phys. Rev. Lett. 56, 930 (1986).
  13. S. S. Nair, S. Wang, and D. C. Hurley, Composites 41, 624 (2010).
  14. W. C. Oliver and G. M. Pharr, J. Mater. Res. 7, 1564 (1992).
  15. O. Piétrement and M. Troyon, J. Colloid Interf. Sci. 226, 166 (2000).
  16. B. Capella and G. Dietler, Surf. Sci. Rep. J. 34, 1 (1999).
  17. J. N. Sharpe, Handbook of Experimental Solid Mechanics (Springer, Berlin, 2008).
  18. J. Crassous, E. Charlaix, H. Gayvallet, and J. L. Loubet, Langmuir 9, 1995 (1993).
  19. R. J. Jaccodine, J. Electrochem. Soc. 110, 524 (1963).
  20. E. Amitay-Sadovsky and H. D. Wagner, Polymer 39, 2387 (1998).
  21. J. G. Williams, Stress Analysis of Polymers (Ellis Horwood, Hempstead, UK, 1980).
  22. H. Cochard, P. Cruiziat, and M. T. Tyree, Plant Physiol. 100, 205 (1992).
  23. J. P. André, Organisation vasculaire des angiospermes: une vision nouvelle (Quae, Versailles, France, 2002).
  24. J. S. Sperry, U. G. Hacke, and J. K. Wheeler, Plant Cell Environ. 28, 456 (2005).
  25. J. K. Wheeler, J. S. Sperry, U. G. Hacke, and N. Hoang, Plant Cell Environ. 28, 800 (2005).
  26. S. P. Timoshenko and S. Woinowsky-Krieger, Theory of Plates and Shells, 2nd ed. (McGraw-Hill International Editions, New York, 1959).
  27. M. Eder, O. Arnould, J. W. C. Dunlop, J. Hornatowska, and L. Salmén, Wood Sci. Technol. 47, 163 (2013).
  28. D. W. Green, J. E. Winandy, and D. E. Kretschmann, in Wood Handbook: Wood as an Engineering Material, Gen. Tech. Rep. FPL-GTR-113 (U.S. Department of Agriculture, Forest Service, Forest Products Laboratory, Madison, WI, 1999), p. 463.
  29. B. Choat, S. Jansen, M. A. Zwieniecki, E. Smets, and N. M. Holbrook, J. Exp. Bot. 55, 1569 (2004).
  30. M. W. Shane, M. E. McCully, and M. J. Canny, Ann. Bot. 85, 613 (2000).
  31. B. Choat, M. Ball, J. Luly, and J. Holtum, Plant Physiol. 131, 41 (2003).
  32. E. Guyon, J. P. Hulin, L. Petit, and C. D. Mitescu, Physical Hydrodynamics (Oxford University Press, Oxford, 2001).
  33. J. Comyn, Polymer Permeability (Chapman & Hall, London, 1985).

Outline

Information

Sign In to Your Journals Account

Filter

Filter

Article Lookup

Enter a citation