Animal morphogenesis arises from the complex interplay between multiple mechanical and biochemical processes with mutual feedback. Developing an effective, coarse-grained description of morphogenesis is essential for understanding how these processes are coordinated across scales to form robust, functional outcomes. Here we show that the nematic order of the supra-cellular actin fibers in regenerating Hydra defines a slowlyvarying field, whose dynamics provide an effective description of the morphogenesis process. We show that topological defects in this field, which are long-lived yet display rich dynamics, act as organization centers with morphological features developing at defect sites. These observations suggest that the nematic orientation field can be considered a "mechanical morphogen" whose dynamics, in conjugation with various biochemical and mechanical signaling processes, result in the robust emergence of functional patterns during morphogenesis.Animal morphogenesis involves multiple mechanical and biochemical processes, spanning several orders of magnitude in space and time, from local dynamics at the molecular level to global, organism-scale morphology. How these numerous processes are coordinated and integrated across scales to form robust, functional outcomes remains an outstanding question [1][2][3][4] .Developing an effective, coarse-grained description of morphogenesis can provide essential insights towards addressing this important challenge. Here, we focus on whole-body regeneration in Hydra, a small fresh-water predatory animal, and provide an effective description of the morphogenesis process that is based on the dynamic organization of the supra-cellular actin fibers in regenerating tissues 5,6 .