Plants constantly undergo external mechanical loads such as wind or touch and respond to these stimuli by acclimating their growth processes. A fascinating feature of this mechanicalinduced growth response is that it can occur rapidly and at long distance from the initial site of stimulation, suggesting the existence of a fast signal that propagates across the whole plant. The nature and origin of the signal is still not understood, but it has been recently suggested that it could be purely mechanical and originate from the coupling between the local deformation of the tissues (bending) and the water pressure in the plant vascular system. Here, we address the physical origin of this hydromechanical coupling using a biomimetic strategy. We designed soft artificial branches perforated with longitudinal liquid-filled channels that mimic the basic features of natural stems and branches. In response to bending, a strong overpressure is generated in the channels that varies quadratically with the bending curvature. A model based on a mechanism analogous to the ovalization of hollow tubes enables us to predict quantitatively this nonlinear poroelastic response and identify the key physical parameters that control the generation of the pressure pulse. Further experiments conducted on natural tree branches reveal the same phenomenology. Once rescaled by the model prediction, both the biomimetic and natural branches fall on the same master curve, enlightening the universality of our poroelastic mechanism for the generation of hydraulic signals in plants.plant biomechanics | biomimetism | long-distance signaling | poroelasticity | nonlinear beams S ince Darwin and Knight (1, 2), scientists have known that plants are able to perceive external mechanical perturbation and respond to these stimuli by modifying their growth, a process called thigmomorphogenesis (3-6). In response to mechanical stress, plants tend to decrease their elongation growth and, for plants having secondary growth like trees, increase the diameter of their organs. Over the past decades, reports have refined our understanding of thigmomorphogenesis at the biomechanical, physiological, and molecular levels (4, 7-12). A remarkable feature of this mechanically induced response is that it can be local and also nonlocal. When a shoot is bent, a sudden arrest of the elongation growth is observed far away from the perturbed area (13) within minutes (8). These experiments demonstrate that plants can carry mechanosensing information over a long distance (from centimeters to meters) very rapidly throughout the whole organ. Among the different hypotheses for this long-distance signaling [hormones transport and electrical signals (14-16)], it has long been argued that hydraulic pulses could provide a unique way for rapid communication in plants, thanks to their highly connected hydraulic network that brings water from the roots to the leaves (16-18). Propagating hydraulic waves were first mentioned by Ricca in the 1920s during his study of the sensitive plant Mimosa ...