4.8 Article

Barium distributions in teeth reveal early-life dietary transitions in primates

Journal

NATURE
Volume 498, Issue 7453, Pages 216-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nature12169

Keywords

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Funding

  1. US Environmental Protection Agency [RD 83171001, RD 82670901]
  2. US National Institutes of Environmental Health Sciences [PO1 ES009605]
  3. NSF [BCS-0921978]
  4. Max Planck Institute for Evolutionary Anthropology
  5. Australian Research Council [DP120101752, LP100200254]
  6. SCU postdoctoral Fellowship grant
  7. National Institute of Environmental Health Sciences [4R00ES019597-03]
  8. NHMRC [APP1028372]
  9. Agilent Technologies
  10. Kennelec Scientific
  11. Australian Research Council [LP100200254] Funding Source: Australian Research Council

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Early-life dietary transitions reflect fundamental aspects of primate evolution and are important determinants of health in contemporary human populations(1,2). Weaning is critical to developmental and reproductive rates; early weaning can have detrimental health effects but enables shorter inter-birth intervals, which influences population growth(3). Uncovering early-life dietary history in fossils is hampered by the absence of prospectively validated biomarkers that are not modified during fossilization(4). Here we show that large dietary shifts in early life manifest as compositional variations in dental tissues. Teeth from human children and captive macaques, with prospectively recorded diet histories, demonstrate that barium (Ba) distributions accurately reflect dietary transitions from the introduction of mother's milk through the weaning process. We also document dietary transitions in a Middle Palaeolithic juvenile Neanderthal, which shows a pattern of exclusive breastfeeding for seven months, followed by seven months of supplementation. After this point, Ba levels in enamel returned to baseline prenatal levels, indicating an abrupt cessation of breastfeeding at 1.2 years of age. Integration of Ba spatial distributions and histological mapping of tooth formation enables novel studies of the evolution of human life history, dietary ontogeny in wild primates, and human health investigations through accurate reconstructions of breastfeeding history.

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