Michael Tabor
Contact
- (520) 621-4664
- ADMINISTRATION, Rm. 601
- TUCSON, AZ 85721-0066
- tabor@arizona.edu
Bio
No activities entered.
Interests
No activities entered.
Courses
No activities entered.
Scholarly Contributions
Journals/Publications
- Tabor, M., Goriely, A., & Tabor, M. -. (2006). Estimates of biomechanical forces in Magnaporthe grisea. Mycological research, 110(Pt 7).More infoThe mechanical actions of the fungus Magnaporthe grisea raise many intriguing questions concerning the forces involved. These include: (1) the material properties of the appressorial wall; (2) the strength of the adhesive that keeps the appressorium anchored to the rice leaf surface; and (3) the forces involved in the penetration process whereby a peg is driven through the host cell wall. In this paper we give order of magnitude estimates for all three of these quantities. A simple Young-Laplace law type argument is used to show that the appressorial wall elastic modulus is of order 10-100 MPa; and an adaptation of standard adhesion theory indicates a lower bound on the strength of the appressorial adhesive to be of the order 500 J/m(2). Drawing on ideas from plasticity theory and ballistics, estimates of the penetration force raise interesting questions about experiments performed on the penetration of inert substrates by the fungus.
- Tabor, M., Tongen, A., Goriely, A., & Tabor, M. -. (2006). Biomechanical model for appressorial design in Magnaporthe grisea. Journal of theoretical biology, 240(1).More infoThe fungus Magnaporthe grisea, commonly referred to as the rice blast fungus, is responsible for destroying from 10% to 30% of the world's rice crop each year. The fungus attaches to the rice leaf and forms a dome-shaped structure, the appressorium, in which enormous pressures are generated that are used to blast a penetration peg through the rice cell walls and infect the plant. We develop a model of the appressorial design in terms of a bioelastic shell that can explain the shape of the appressorium, and its ability to maintain that shape under the enormous increases in turgor pressure that can occur during the penetration phase.
- Tabor, M., Goriely, A., Károlyi, G., & Tabor, M. -. (2005). Growth induced curve dynamics for filamentary micro-organisms. Journal of mathematical biology, 51(3).More infoThe growth of filamentary micro-organisms is described in terms of the geometry of evolving planar curves in which the dynamics is determined by an underlying growth process. Steadily propagating tip shapes in two and three dimensions are found that are consistent with experimentally observed growth sequences.
- Tabor, M., Goriely, A., & Tabor, M. -. (2003). Biomechanical models of hyphal growth in actinomycetes. Journal of theoretical biology, 222(2).More infoThe tip growth of filamentary actinomycetes is investigated within the framework of large deformation membrane theory in which the cell wall is represented as a growing elastic membrane with geometry-dependent elastic properties. The model exhibits realistic hyphal shapes and indicates a self-similar tip growth mechanism consistent with that observed in experiments. It also demonstrates a simple mechanism for hyphal swelling and beading that is observed in the presence of a lysing agent.
- Tabor, M., Goriely, A., & Tabor, M. -. (2003). Self-similar tip growth in filamentary organisms. Physical review letters, 90(10).More infoThe growth of a family of filamentary microorganisms is described in terms of self-similar growth at the tip which is driven by pressure and sustained by a wall-building growth process. The cell wall is modeled biomechanically as a stretchable elastic membrane using large-deformation elasticity theory. Incorporation of geometry dependent elastic moduli and a self-similar ansatz shows how these equations can generate realistic tip shapes corresponding to a self-similar expansion process.