A Natural Programmable Metamaterial Controls 3D Curvature of Compound Eyes
The panoramic vision of the convex compound eyes, common to insects and crustaceans, relies on micrometer-scale curvature variations1. These variations create specialized visual zones adapted to specific tasks, including detecting prey, mates, or predators2,3. However, the mechanisms by which such fine-scale curvature is encoded during development remain unknown. Here we show that the developing eye of Drosophila melanogaster functions as a natural metamaterial that programs the organs precise 3D curvature. We discover a supracellular triangular mesh in the basal retina with a specific pattern of triangles sizes. Computational simulations demonstrate its role directing the small scale curvature variations of the eye. Genetic disruption of this micropattern prevents local curvature establishment. Furthermore, the presence of a homologous mesh-curvature relationship in Drosophila mauritiana indicates evolutionary conservation of this mechanism. These results reveal a novel mechanism of morphogenesis control in which the supracellular 2D patterning give rise to a biological programmable metamaterial that encodes 3D curvature with great precision4. Our in vivo finding offers a novel framework for the design of shape-programmable 3D biological surfaces with broad implications from synthetic morphogenesis to clinical applications.