This paper analyzes indicators of developmental stress in relation to known individual pathologies and developmental patterns in the cranium, vertebrae, and long bones; it presents its analysis using the lenses of ontogeny and life-course to incorporate information about individual histories and study the origins of those developmental patterns.
Skeletal indicators of developmental stress are commonly used to assess health, disease, and patterns of morbidity and mortality in past populations. Incorporating information about individual life history, such as adverse life events, allows for a more thorough understanding of their etiology. This paper adopts the double lens of ontogeny and the life course to analyze indicators of developmental stress in relation to known individual pathologies and developmental patterns of the cranium, vertebrae, and long bones. Six skeletal indicators were collected on CT scans or virtual skeletal reconstructions of 1033 contemporary deceased male and female individuals aged between 0 and 20 years from New Mexico: cribra orbitalia, porotic hyperostosis, Harris lines, stunting, vertebral neural canal diameters, and bone mineral density. Autopsy reports provided information on age, sex, disease type, and duration. Polychoric and polyserial correlations, boxplots, balloon plots, factor analyses of mixed data, and cluster analyses were used to explore patterns among indicators, ontogeny, sex, and disease. The presence and prevalence of indicators varied depending on age and disease: Harris lines, stunted growth, and cribra orbitalia were common in younger age groups and in cases of long-term or respiratory illnesses, while porotic hyperostosis was more prevalent in adolescent and young adult males. Skeletal indicators of developmental stress are most likely associated with the timing of adverse life events in relation to the corresponding ontogenetic patterns, developmental sensitivity to stressors, and developmental plasticity/canalization of the different skeletal elements that bear them. (Published Abstract Provided)