“…Thus, the evolutionary presence or absence of secondary cartilage on the coronoid process reflects species-specific variation in functional anatomy determined by in ovo mechanical loading (Beresford, 1981; Fang and Hall, 1997; Hall, 1979; Stutzmann and Petrovic, 1975). In taxa such as humans, rats, cats, and duck, secondary cartilage forms at the jaw adductor muscle insertion (Amorim et al, 2010, 2008; Hall, 2005; Horowitz and Shapiro, 1951; Kantomaa and Rönning, 1997; Moore, 1973, 1981; Solem et al, 2011; Soni and Malloy, 1974; Vinkka, 1982; Washburn, 1947) whereas an equivalent secondary cartilage is absent in mice, guinea pigs, chick, and quail (Anthwal et al, 2008, 2015; Boyd et al, 1967; Moss and Meehan, 1970; Rot-Nikcevic et al, 2007; Shibata et al, 2003; Solem et al, 2011). Our work implies that the reason secondary cartilage forms at this location in some species and not others is due to the way embryonic motility interacts with NCM-mediated muscle pattern to create differential forces.…”