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Craig Brodersen

Publications and source records attributed to Craig Brodersen.

2 recordsLinked to original sources

Self-Buckling of Pressurized Cylindrical Tubes

We investigate the buckling of hollow cylindrical tubes subject to their own weight and internal pressure, inspired by the columnar cells of the palisade mesophyll in dicotyledon leaves which resemble pressurized cylindrical tubes. When the internal pressure in the cylinder is equal to the outside pressure, the problem is usually termed self-buckling, which has been studied extensively for solid rods, hollow cylinders, and thin cylindrical shells. Specifically, we perform FEM simulations and desktop-scale experiments to determine the instability thresholds for different geometrical parameters. We first test our models against self-buckling results without pressure for solid rods and hollow cylindrical tubes, and then proceed to determine the critical buckling pressure for a set of material and geometrical parameters. We find that positive internal pressures can stiffen cylinders that are unstable under their own weight, leading to an effective Young's modulus that we show scales linearly with the applied pressure. On the contrary, cylinders that are stable under self-weight, buckle under a negative pressure, resembling classical results on pressure-induced ring buckling. Our findings offer new insights on the interplay between gravity and pressure for the mechanical instability of hollow cylindrical tubes, which we hope will be useful for the study of both engineering and biological structures under similar loads.

cond-mat.soft

Localized growth drives spongy mesophyll morphogenesis

The spongy mesophyll is a complex, porous tissue found in plant leaves that enables carbon capture and provides mechanical stability. Unlike many other biological tissues, which remain confluent throughout development, the spongy mesophyll must develop from an initially confluent tissue into a tortuous network of cells with a large proportion of intercellular airspace. How the airspace in the spongy mesophyll develops while the cells remain mechanically stable remains unknown. Here, we used computer simulations of deformable particles to develop a purely mechanical model for the development of the spongy mesophyll tissue. By stipulating that (1) cell perimeter grows only near voids, (2) cells both form and break adhesive bonds, and (3) the tissue pressure remains constant, the computational model was able to recapitulate the developmental trajectory of the microstructure of the spongy mesophyll observed in Arabidopsis thaliana leaves. Robust generation of pore space in the spongy mesophyll requires a balance of cell growth, adhesion, stiffness and tissue pressure to ensure cell networks remain both porous yet mechanically robust. The success of this mechanical model of tissue growth and porosity evolution suggests that simple physical principles can coordinate and drive the development of complex plant tissues like the spongy mesophyll.

physics.bio-ph