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Japanese macaques are ideal to advance understanding of a wide‐spread pattern of recurrent developmental distress in great apes, preserved as repetitive linear enamel hypoplasia (rLEH). Not only are they numerous, unendangered, and well‐studied, but they are distributed from warm‐temperate evergreen habitats in southern Japan to cool‐temperate habitats in the north, where they are adapted behaviorally and phenotypically to winter cold and seasonal undernutrition. We provide a pilot study to determine if enamel hypoplasia exists in Japanese macaques from the north and, if temporal patterns of enamel hypoplasia are consistent with seasonal cold, undernutrition and/or exposure to secondary plant compounds. High‐resolution casts of canine teeth from 15 males obtained from Shimokita Peninsula (latitude 41.3° N) between 2012 and 2014, whose skeletons are curated at the Center for the Evolutionary Origins of Human Behavior, Kyoto University, were imaged by confocal and scanning electron microscopy. Perikymata, the surface expression of regularly deposited imbricational layers of enamel, provide an estimate of time between and within hypoplastic enamel defects. Based on histological sections from five individuals, we determined Retzius periodicity to be 7 days. Evidence for recurrence, duration, and severity of 68 LEH defects was collected from perikymata counts as well as measurements of LEH angle of onset, depth and width. Male canine teeth show four to five recurrent, evenly‐spaced enamel defects per crown with a median of 54.8 (range 18–74) perikymata between defects; lasting on average 8.7 (range 1–20) perikymata. These translate into repetitive developmental distress averaging every 1.05 years, lasting 8.7 weeks, less than local winter foraging conditions (100 days). We conclude that linear enamel hypoplasia recurs circ‐annually among high‐latitude male monkeys from Japan. The triad of cold, hunger and anti‐feedants can be differentiated in future study through recourse to provisioned and un‐provisioned populations throughout the Japanese archipelago.
Japanese macaques are ideal to advance understanding of a wide‐spread pattern of recurrent developmental distress in great apes, preserved as repetitive linear enamel hypoplasia (rLEH). Not only are they numerous, unendangered, and well‐studied, but they are distributed from warm‐temperate evergreen habitats in southern Japan to cool‐temperate habitats in the north, where they are adapted behaviorally and phenotypically to winter cold and seasonal undernutrition. We provide a pilot study to determine if enamel hypoplasia exists in Japanese macaques from the north and, if temporal patterns of enamel hypoplasia are consistent with seasonal cold, undernutrition and/or exposure to secondary plant compounds. High‐resolution casts of canine teeth from 15 males obtained from Shimokita Peninsula (latitude 41.3° N) between 2012 and 2014, whose skeletons are curated at the Center for the Evolutionary Origins of Human Behavior, Kyoto University, were imaged by confocal and scanning electron microscopy. Perikymata, the surface expression of regularly deposited imbricational layers of enamel, provide an estimate of time between and within hypoplastic enamel defects. Based on histological sections from five individuals, we determined Retzius periodicity to be 7 days. Evidence for recurrence, duration, and severity of 68 LEH defects was collected from perikymata counts as well as measurements of LEH angle of onset, depth and width. Male canine teeth show four to five recurrent, evenly‐spaced enamel defects per crown with a median of 54.8 (range 18–74) perikymata between defects; lasting on average 8.7 (range 1–20) perikymata. These translate into repetitive developmental distress averaging every 1.05 years, lasting 8.7 weeks, less than local winter foraging conditions (100 days). We conclude that linear enamel hypoplasia recurs circ‐annually among high‐latitude male monkeys from Japan. The triad of cold, hunger and anti‐feedants can be differentiated in future study through recourse to provisioned and un‐provisioned populations throughout the Japanese archipelago.
ObjectivesReconstruction of life histories for fossil and living primates draws on rate of enamel layering, termed Retzius periodicity (RP in days) expressed as surface perikymata, during dental crown formation. Disclosure of RP through thin sectioning is destructive; consequently, sample sizes are inadequate to detect the range of RPs present in discrete taxa. We propose an additional method to detect RPs at the population level based on twice‐yearly average recurrence of linear enamel hypoplasia (rLEH) in apes shown by prior studies.Materials and MethodsCasts of teeth from orangutans (Pongo pygmaeus) (n = 40) and Lufengpithecus lufengensis (n = 57) from Late Miocene Shihuiba, China, (133 and 138 LEH, respectively) were recorded with scanning electron microscope (SEM) and confocal microscopy to yield perikymata counts between episodes of LEH. Frequency distributions of aggregated perikymata counts between LEH were compared to frequency distribution of tooth‐specific ratios of perikymata counts between successive LEH (this latter step removes effects of RP differences within a sample).ResultsDrawing on prior research, two successive intervals between LEH span 1 year on average. Ratios of successive to previous intervals between LEH show that orangutans and Lufengpithecus exhibit two asymmetric intervals centered on 5.3 and 6.7 months, likely reflecting the effect of axial tilt insolation on phenology. Estimated RPs are not unimodal but show a range from 7 to 12 in Lufenpithecus and 8 to 11 in Pongo, comparable to published values.DiscussionRepetitive LEH is sufficiently regular to detect additional RPs which, in the case of Lufengpithecus, have yet to be demonstrated histologically.
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