Fig. 1.

Overview of the experimental workflow from left to right: a A section was cut from the midshaft of a human femur and stained with rhodamine before embedding. b A 2D overview image of whole specimen was made using confocal laser scanning microscopy (CLSM) in order to identify ordinary osteons and osteon-in-osteons. 3D image stacks of the selected osteons were taken using CLSM. c The cement line (red 3D surface) and Haversian canal (blue 3D surface) in each osteon were marked as boundaries for the computational models. Both surfaces appear as areas and not as lines due to the considered depth of the image. d The 3D CLSM images were converted into networks consisting of edges (lines representing the canaliculi) and nodes (spheres where canaliculi intersect). A fluid flow analysis was then performed on these networks. Colors of spheres in d represent the node pressure, while the darkness of the lines represents the canalicular fluid flow velocity