Crystallization of ACP with timeTo probe the stability of the observed ACP in disordered phase with respect to the adjacent HA nanocrystals, we performed TEM analysis of the same region after a 30-day time lapse. During the 30 days, the TEM sample was stored at room temperature in a N2 environment. Figure S1a shows the initial arrangement of ACP (left) and HA nanocrystals (right), as well as the diffraction pattern inset showing the crystallinity of the HA. Figure S1b shows the same region after the 30 day incubation period; the HA nanocrystals on the right appear to have grown, confirmed by the increased (112), (211), (300) intensities in the diffraction pattern inset; we also observe the emergence of (002) reflections after one month, which further proves the formation of crystals. These results demonstrate suggest that biogenic ACP is a precursor for crystalline cHA formation in bone in the observed conditions, as similarly observed by Mahamid et al 1 . Figure S1. Time lapse micrographs of amorphous and nanocrystalline regions. Deprotonated mineral structure in disordered phase taken before (a) and after (b) a 30 day incubation at room temperature in a nitrogen environment. The electron diffraction pattern after the incubation (b, inset) shows an increase in crystallinity as evidenced by more intense HA reflections and the emergence of the (002) spots when compared to the initial diffraction pattern (a, inset).
Size Dependent Model ConstructionWe propose that the yield strength, , decreases as the probability of having a flaw (i.e. a pore) on the pillar surface increases; that is, surface flaws serve as probabilistic stress concentrators, which initiate failure during compression. This is manifested most prevalently in the larger pillars, with diameters > 500nm. At these nano and micro length scales, it is reasonable to consider bone as a fiber-