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Geitmann, A.

Publications and source records attributed to Geitmann, A..

3 recordsLinked to original sources

Microscale geometrical features in the plant leaf epidermis confer enhanced resistance to mechanical failure

In many plant species, epidermal tissues of leaves and petals feature irregular wavy cell geometries forming jigsaw puzzle patterns. At the origin of plant tissues are simple polyhedral progenitor cells that divide and grow into a kaleidoscopic array of morphologies that underpin plant organ functionality. The wide prevalence and great diversity of the wavy cell shape in the plant kingdom point to the significance of this trait and its tunability by environmental pressures. Despite multiple attempts to explain the advent of this complex cell geometry by evolutionary relevant functionality, our understanding of this peculiar tissue patterning preserved through evolution remains lacking. Here, by combining microscopic and macroscopic fracture experiments with computational fracture mechanics, we show that wavy epidermal cells toughen the plants protective skin. Based on a multi-scale approach, we demonstrate that, biological and synthetic materials alike can be toughened through an energy-efficient patterning process. Our data reveal a ubiquitous and tunable structural-mechanical mechanism employed in the macro-scale design of plants to protect them from the detrimental effects of surface fissures and to enable and guide the direction of beneficial fractures. We expect these data to inform selective plant breeding for traits enhancing plant survival under changing environmental conditions. From a materials engineering perspective, this work exemplifies that plants hold sophisticated design principles to inspire human-made materials.

plant biology↗

Multiscale structural control of hydraulic bending in the sensitive plant Mimosa pudica

Pulvini are joint-like motor organs that power active leaf movement in many plants. Multiple structural specializations spanning subcellular, cellular, and tissue scales of pulvinus organization have been described; however, the impacts of multiscale mechanics on pulvinus physiology remain poorly understood. To investigate the influence of multiscale morphology on turgor-induced deformation, we visualized Mimosa pudica pulvinus morphology at multiple hierarchical scales of organization and used osmotic perturbations to experimentally swell pulvini in incremental states of dissection. We observed directional cellulose microfibril reinforcement, oblong, spindle-shaped primary pit fields, and flattened, disk-like cell geometries in the parenchyma of M. pudica. Consistent with these observations, isolated parenchyma tissues displayed highly anisotropic swelling behaviors indicating a high degree of mechanical anisotropy. Swelling behaviors at higher scales of pulvinus organization were also influenced by the presence of the pulvinus epidermis, which displayed oblong epidermal cells oriented transverse to the pulvinus long axis. Our findings indicate that structural specializations spread across multiple hierarchical scales of organization guide hydraulic deformation of pulvini, suggesting that multiscale mechanics are crucial to the translation of cell-level turgor variations into organ-scale pulvinus motion in vivo.

plant biology↗

Mechanical stress initiates and sustains the morphogenesis of wavy leaf epidermal cells

Plant cell morphogenesis is governed by the mechanical properties of the cell wall and the resulting cell shape is intimately related to the respective specific function. Pavement cells covering the surface of plant leaves form wavy interlocking patterns in many plants. We use computational mechanics to simulate the morphogenetic process based on experimentally assessed cell shapes, growth dynamics, and cell wall chemistry. The simulations and experimental evidence suggest a multistep process underlying the morphogenesis of pavement cells during tissue differentiation. The mechanical shaping process relies on spatially confined, feedback-augmented stiffening of the cell wall in the periclinal walls, an effect that correlates with experimentally observed deposition patterns of cellulose and de-esterified pectin. We provide evidence for mechanical buckling of the pavement cell walls that can robustly initiate patterns de novo and may precede chemical and geometrical anisotropy.\n\nHighlightsO_LIA multistep mechano-chemical morphogenetic process underlies the wavy pattern of epidermal pavement cells.\nC_LIO_LIMicrotubule polarization is preceded by an event that breaks mechanical isotropy in the cell wall.\nC_LIO_LIMechanical models simulate the formation of wavy cell shapes, predict buckling of the cell walls and spatially confined variations in the mechanical properties of leaf epidermal cells.\nC_LIO_LIStress/strain stiffening following the buckling of the cell walls constitutes a crucial element in a positive feedback loop forming interlocking pavement cells.\nC_LIO_LIPolarization of cortical microtubules, cellulose microfibrils, and de-esterified pectin occur at the necks of wavy pavement cells, matching the in silico prediction of cell wall stiffening.\nC_LI

plant biology↗