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- All Subjects: Evolution & development
Description
Fundamental hypotheses about the life history, complex cognition and social dynamics of humans are rooted in feeding ecology - particularly in the experiences of young animals as they grow. However, the few existing primate developmental data are limited to only a handful of species of monkeys and apes. Without comparative data from more basal primates, such as lemurs, we are limited in the scope of our understanding of how feeding has shaped the evolution of these extraordinary aspects of primate biology. I present a developmental view of feeding ecology in the ring-tailed lemur (Lemur catta) using a mixed longitudinal sample (infant through adult) collected at the Beza Mahafaly Special Reserve in southwestern Madagascar from May 2009 to March 2010. I document the development of feeding, including weaning, the transition to solid food, and how foods are included in infant diets. Early in juvenility ring-tailed lemurs efficiently process most foods, but that hard ripe fruits and insects require more time to master. Infants and juveniles do not use many of the social learning behaviors that are common in monkeys and apes, and instead likely rely both on their own trial and error and simple local enhancement to learn appropriate foods. Juvenile ring-tailed lemurs are competent and efficient foragers, and that mitigating ecological risks may not best predict the lemur juvenile period, and that increases in social complexity and brain size may be at the root of primate juvenility. Finally, from juvenility through adulthood, females have more diverse diets than males. The early emergence of sex differences in dietary diversity in juvenility that are maintained throughout adulthood indicate that, in addition to reproductive costs incurred by females, niche partitioning is an important aspect of sex differential feeding ecology, and that ontogenetic studies of feeding are particularly valuable to understanding how selection shapes adult, species-typical diets. Overall, lemur juvenility is a time to play, build social relationships, learn about food, and where the kernels of sex-typical feeding develop. This study of the ontogeny of feeding ecology contributes an important phylogenetic perspective on the relationship between juvenility and the emergent foraging behaviors of developing animals
ContributorsO'Mara, Michael Teague (Author) / Nash, Leanne T. (Thesis advisor) / Reed, Kaye E (Committee member) / Schwartz, Gary T (Committee member) / Sauther, Michelle L (Committee member) / Arizona State University (Publisher)
Created2012
Description
Across primates, molar-emergence age is strongly correlated to life-history variables, such as age-at-first-reproduction and longevity. This relationship allows for the reconstruction of life-history parameters in fossil primates. The mechanism responsible for modulating molar-emergence age is unknown, however. This dissertation uses a biomechanical model that accurately predicts the position of molars in adults to determine whether molar emergence is constrained by chewing biomechanics throughout ontogeny. A key aspect of chewing system configuration in adults is the position of molars: the distal-most molar is constrained to avoid tensile forces at the temporomandibular joint (TMJ). Using three-dimensional data from growth samples of 1258 skulls, representing 21 primate species, this research tested the hypothesis that the location and timing of molar emergence is constrained to avoid high and potentially dangerous tensile forces at the TMJ throughout growth. Results indicate that molars emerge in a predictable position to safeguard the TMJ during chewing. Factors related to the size of the buffer zone, a safety feature that creates greater stability at the TMJ during biting, account for a large portion of both ontogenetic and interspecific variation in the position of emergence. Furthermore, the rate at which space is made available in the jaws and the duration of jaw growth both determine the timing of molar emergence. Overall, this dissertation provides a mechanical and developmental model for explaining temporal and spatial variation in molar emergence and a framework for understanding how variation in the timing of molar emergence has evolved among primates. The findings suggest that life history is related to ages at molar emergence through its influence on the rate and duration of jaw growth. This dissertation provides support for the functionally integrated nature of craniofacial growth and has implications for the study of primate life history evolution and masticatory morphology in the fossil record.
ContributorsGlowacka, Halszka (Author) / Schwartz, Gary T (Thesis advisor) / Kimbel, William H. (Committee member) / Reed, Kaye E (Committee member) / Wright, Barth W (Committee member) / Arizona State University (Publisher)
Created2017