“…Long‐term data accumulating across great ape study sites is demonstrating considerable diversity in life history characteristics within and among species (Breuer et al, ; Robbins et al, ; Stoinski, Perdue, Breuer, & Hof, ), and in other factors such as habitat use, daily travel distance, feeding ecology, arboreality and energy intake rate, which are relevant to understanding life history strategies (e.g., Doran et al, ; Leigh & Blomquist, ; Masi, Cipolletta, & Robbins, ; Rogers et al, ; Wich et al, ; van Noordwijk & van Schaik, ; Wright et al, ). However, quantitative studies of the physical growth and development of known‐aged great apes have been overwhelmingly derived from captive environments or less well documented museum collections (e.g., Shea, ; Taylor, ), with notable exceptions [e.g., orangutan arm length (Schuppli et al, ); chimpanzee body weight, linear dimensions, brain size and tooth emergence (e.g., Machanda et al, ; Neubauer, Gunz, Schwarz, Hublin, & Boesch, ; Pusey, Oehlert, Williams, & Goodall, ; Smith & Boesch, ; Smith et al, ; Zihlman, Bolter, & Boesch, ); western gorilla body length (Breuer et al, ); mountain gorilla brain size and dental development (McFarlin et al, ; Kralick et al, 2017)]. As captive environments differ significantly from natural settings, systematic investigations of factors influencing variation in postnatal ontogeny in the wild are critical for a comprehensive understanding of socio‐ecological influences on ape life history and a more salient comparative framework for understanding human life history evolution.…”