Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-tn8tq Total loading time: 0 Render date: 2024-06-20T11:53:46.375Z Has data issue: false hasContentIssue false

4 - Using perikymata to estimate the duration of growth disruptions in fossil hominin teeth: issues of methodology and interpretation

Published online by Cambridge University Press:  12 September 2009

Debbie Guatelli-Steinberg
Affiliation:
Department of Anthropology 244 Lord Hall, 124 West 17th Avenue, The Ohio State University, Columbus, Ohio 43210, USA
Joel D. Irish
Affiliation:
University of Alaska, Fairbanks
Greg C. Nelson
Affiliation:
University of Oregon
Get access

Summary

Introduction

Enamel hypoplasias are developmental defects of tooth enamel taking the form of pits, horizontal lines, grooves, or, occasionally, altogether missing enamel (FDI DDE Index, 1982, 1992). These defects result from disturbances to ameloblasts (enamel-producing cells) during the secretory phase of enamel formation (Goodman and Rose, 1990; Ten Cate, 1994). When systemic physiological stress, such as malnutrition or illness, disturbs enamel formation, all crowns forming during the period of stress are likely to develop enamel hypoplasias (Hillson, 1996). Once formed, these defects become permanent features of the crown, unless worn away by abrasion or attrition. For these reasons, and because teeth are the most abundant of skeletal remains (Hillson, 1996), enamel hypoplasias have become one of the most important sources of information about systemic physiological stress in fossil hominins (Bailey and Hublin, 2006; Bombin, 1990; Brennan, 1991; Brunet et al., 2002; Guatelli-Steinberg 2003, 2004; Guatelli-Steinberg et al., 2004; Hutchinson et al., 1997; Moggi-Cecchi, 2000; Molnar and Molnar, 1985; Ogilvie et al., 1989; Tobias, 1991; White, 1978).

Linear enamel hypoplasia (LEH) is the most common type of hypoplastic defect, taking the form of “furrows” on the enamel surface (Hillson and Bond, 1997). Of the different types of hypoplastic defects, LEH has the greatest potential to reveal information about the duration of enamel growth disturbances. This potential resides in several crucial facts about enamel formation and in the nature of LEH defects themselves.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aiello, L. and Dean, M. C. (2002). An Introduction to Human Evolutionary Anatomy. London: Academic PressGoogle Scholar
Bailey, S. E. and Hublin, J.-J. (2006). Dental remains from the Grotte du Renne at Arcy-sur-Cure (Yonne). Journal of Human Evolution, 50, 485–508CrossRefGoogle Scholar
Blakey, M. L., Leslie, T. E., and Reidy, J. P. (1994). Frequency and chronological distribution of dental enamel hypoplasia in enslaved African Americans: a test of the weaning hypothesis. American Journal of Physical Anthropology, 95, 371–84CrossRefGoogle ScholarPubMed
Beynon, D. and Dean, M. C. (1988). Distinct dental development patterns in early fossil hominids. Nature, 335, 509–14CrossRefGoogle ScholarPubMed
Bombin, M. (1990). Transverse enamel hypoplasia on teeth of South African Plio-Pleistocene hominids. Naturwissenschaften, 77, 128–9CrossRefGoogle ScholarPubMed
Bocherens, H., Billiou, D., Mariotti, A.et al. (1999). Paleoenvironmental and paleodietary implications of isotopic biogeochemistry of last interglacial Neanderthal and mammal bones in Scladina Cave (Belgium). Journal of Archaeological Science, 26, 599–607CrossRefGoogle Scholar
Brennan, M. (1991). Health and Disease in the Middle and Upper Paleolithic of Southwestern France: A Bioarchaeological Study. Ph. D. Dissertation, New York UniversityGoogle Scholar
Bromage, T. G. (1991). Enamel incremental periodicity in the pig-tailed macaque: a polychrome fluorescent labeling study of dental hard tissues. American Journal of Physical Anthropology, 86, 205–14CrossRefGoogle Scholar
Bromage, T. G. and Dean, M. C. (1985). Re-evaluation of the age at death of immature fossil hominids. Nature, 317, 525–7CrossRefGoogle ScholarPubMed
Brunet, M., Fronty, P., Sapanet, M., Bonis, L., and Viriot, L (2002). Enamel hypoplasia in a Pliocene Hominid from Chad. Connective Tissue Research, 43, 94–7CrossRefGoogle Scholar
Dean, M. C. and Reid, D. J. (2001a). Perikymata spacing and distribution on hominid anterior teeth. American Journal of Physical Anthropology, 116, 209–15CrossRefGoogle Scholar
Dean, M. C. and Reid, D. J. (2001b). Anterior tooth formation in Australopithecus and Paranthropus. In Dental Morphology, ed. Brook, A.. Sheffield: University of Sheffield, pp. 135–43Google Scholar
Dean, M. C., Leakey, M. G., Reid, D. J.et al. (2001). Growth processes in teeth distinguish modern humans from Homo erectus and earlier hominins. Nature, 414, 628–31CrossRefGoogle ScholarPubMed
Ensor, B. E. and Irish, J. D. (1995). Hypoplastic area method for analyzing dental enamel hypoplasia. American Journal of Physical Anthropology, 98, 507–18CrossRefGoogle ScholarPubMed
Fédération Dentaire Internationale (1982). An epidemiological index of developmental defects of dental enamel (DDE). International Dental Journal, 32, 159–67
Fédération Dentaire Internationale (1992). A review of the developmental defects of enamel index (DDE Index). International Dental Journal, 42, 411–26
Fitzgerald, C. M. (1998). Do enamel microstructures have regular time dependency? Journal of Human Evolution, 35, 371–86CrossRefGoogle ScholarPubMed
Goodman, A. H. and Rose, J. C. (1990). Assessment of physiological perturbations from dental enamel hypoplasia and associated histological structures. Yearbook of Physical Anthropology, 33, 59–110CrossRefGoogle Scholar
Grine, F. E. (1986). Dental evidence for dietary differences in Australopithecus and Paranthropus: a quantitative analysis of permanent molar microwear. Journal of Human Evolution, 15, 783–822CrossRefGoogle Scholar
Grine, F. E. and Kay, R. F. (1988). Early hominid diets from quantitative image analysis of dental microwear. Nature, 333, 765–8CrossRefGoogle ScholarPubMed
Guatelli-Steinberg, D. (2000). Linear enamel hypoplasia in gibbons (Hylobates lar carpenteri). American Journal of Physical Anthropology, 112, 395–4103.0.CO;2-H>CrossRefGoogle Scholar
Guatelli-Steinberg, D. (2003). Macroscopic and microscopic analyses of linear enamel hypoplasia in Plio-Pleistocene South African hominins with respect to aspects of enamel development and morphology. American Journal of Physical Anthropology, 120, 309–22CrossRefGoogle ScholarPubMed
Guatelli-Steinberg, D. (2004). Analysis and significance of linear enamel hypoplasia in Plio-Pleistocene hominins. American Journal of Physical Anthropology, 123, 199–215CrossRefGoogle ScholarPubMed
Guatelli-Steinberg, D., Larsen, C. S., and Hutchinson, D. L. (2004). Prevalence and duration of linear enamel hypoplasia: a comparative study of Neanderthals and Inuit foragers. Journal of Human Evolution, 47, 65–84CrossRefGoogle Scholar
Guatelli-Steinberg, D., Reid, D. J., Bishop, T. A., and Larsen, C. S. (in press). Imbricational enamel formation in Neandertals and recent modern humans. In Dental Perspectives on Human Evolution: State of the Art Research in Dental Anthropology, ed. Bailey, S. and Hublin, J.-J.. New York: Springer-VerlagGoogle Scholar
Hillson, S. (1992). Impression and replica methods for studying hypoplasia and perikymata on human tooth crown surfaces from archaeological sites. International Journal of Osteoarchaeology, 2, 65–78CrossRefGoogle Scholar
Hillson, S. (1996). Dental Anthropology. Cambridge: Cambridge University PressCrossRefGoogle Scholar
Hillson, S. and Bond, S. (1997). The relationship of enamel hypoplasia to the pattern of tooth crown growth: a discussion. American Journal of Physical Anthropology, 104, 89–1033.0.CO;2-8>CrossRefGoogle ScholarPubMed
Hillson, S. and Jones, B. K. (1989). Instruments for measuring surface profiles: an application in the study of ancient human tooth crown surfaces. Journal of Archaeological Science, 16, 95–105CrossRefGoogle Scholar
Hutchinson, D. L., Larsen, C. S., and Choi, I. (1997). Stressed to the max? Physiological perturbation in the Krapina Neandertals. Current Anthropology, 38, 904–14CrossRefGoogle Scholar
Jelinek, A. J. (1994). Hominids, energy, environment, and behavior in the Late Pleistocene. In Origins of Anatomically Modern Humans, ed. Nitecki, M. H. and Nitecki, D. V.. New York: Plenum Press, pp. 67–92CrossRefGoogle Scholar
King, T., Hillson, S. W., and Humphrey, L. T. (2002). A detailed study of enamel hypoplasia in a post-medieval adolescent of known age and sex. Archives of Oral Biology, 47, 29–39CrossRefGoogle Scholar
Larsen, H. and Rainey, F. (1948). Ipiutak and the Arctic whale hunting culture. Anthropological Papers of the American Museum of Natural History, 42, 1–276Google Scholar
Moggi-Cecchi, J. (2000). Enamel hypoplasia in South African early hominids: A reappraisal. American Journal of Physical Anthropology, 30, 230–1 (abstract)Google Scholar
Molnar, S. and Molnar, I. M. (1985). The prevalence of enamel hypoplasia among the Krapina Neandertals. American Journal of Physical Anthropology, 87, 536–49CrossRefGoogle Scholar
Ogilvie, M. D., Curran, B. K., and Trinkaus, E. (1989). Prevalence and patterning of dental enamel hypoplasia among the Neandertals. American Journal of Physical Anthropology, 79, 25–41CrossRefGoogle ScholarPubMed
Reid, D. J. and Dean, M. C. (2000). Brief communication: the timing of linear hypoplasias on human anterior teeth. American Journal of Physical Anthropology, 113, 135–93.0.CO;2-A>CrossRefGoogle ScholarPubMed
Reid, D. J. and Dean, M. C. (2006). Population variation in human enamel formation. Journal of Human Evolution, 50, 329–46CrossRefGoogle Scholar
Richards, M. P., Petit, P. B., Trinkaus, E.et al. (2000). Neanderthal diet at Vindija and Neanderthal predation: the evidence from stable isotopes. Proceedings of the National Academy of Sciences, 97, 7663–6CrossRefGoogle ScholarPubMed
Rink, W. J., Schwartz, H. P., Smith, F. H., and Radovčić, J. (1995). ESR ages for Krapina hominids. Nature, 378, 24CrossRefGoogle ScholarPubMed
Schwartz, J. H. and Tattersall, I. (2002). The Human Fossil Record. Vol. 1. New York: Wiley-LissGoogle Scholar
Schwartz, J. H., Brauer, J., and Gordon-Larsen, P. (1995). Brief communication: Tigaran (Point Hope, Alaska) tooth drilling. American Journal of Physical Anthropology, 97, 77–82CrossRefGoogle ScholarPubMed
Scott, R. S., Ungar, P. S., Bergstrom, T. S.et al. (2005). Dental microwear texture analysis shows within-species dietary variability in fossil hominins. Nature, 436, 693–5CrossRefGoogle ScholarPubMed
Skinner, M. (1996). Developmental stress in immature hominins from Late Pleistocene Eurasia: Evidence from enamel hypoplasia. Journal of Archaeological Science, 23, 833–52CrossRefGoogle Scholar
Smith, T., Reid, D. J., Dean, M. C. et al. (in press). New perspectives on chimpanzee and human molar development. In Dental Perspectives on Human Evolution: State of the Art Research in Dental Anthropology, ed. Bailey, S. and Hublin, J.-J.. New York: Springer-VerlagGoogle Scholar
Soffer, O. (1994). Ancestral lifeways in Eurasia: The Middle and Upper Paleolithic records. In Origins of Anatomically Modern Humans, ed. Nitecki, M. H. and Nitecki, D. V.. New York: Plenum Press, pp. 84–109CrossRefGoogle Scholar
Sorensen, M. V. and Leonard, W. R. (2001). Neandertal energetics and foraging efficiency. Journal of Human Evolution, 40, 483–95CrossRefGoogle ScholarPubMed
Sponheimer, M. and Lee-Thorp, J. A. (1999). Isotopic evidence for the diet of an early hominid, Australopithecus africanus. Science, 283, 368–370Google ScholarPubMed
Ten, Cate A. R. (1994). Oral Histology: Development, Structure, and Function, 4th edn. St. Louis: CV MosbyGoogle Scholar
Tobias, P. V. (1991). Olduvai Gorge Vol. 4: The Skulls, Endocasts, and Teeth of Homo habilis. Cambridge: Cambridge University PressGoogle Scholar
Trinkaus, E. (1986). The Neandertals and modern human origins. Annual Review of Anthropology, 15, 193–218CrossRefGoogle Scholar
Trinkaus, E. (1989). The Upper Pleistocene transition. In The Emergence of Modern Humans: Biocultural Adaptation in the Later Pleistocene, ed. Trinkaus, E.. New York: Cambridge University Press, pp. 42–6Google Scholar
White, T. D. (1978). Early hominid enamel hypoplasia. American Journal of Physical Anthropology, 49, 79–84CrossRefGoogle ScholarPubMed
Wood, J. W., Harpending, H. C., Weiss, K. M., and Milner, G. R. (1992). The osteological paradox: Problems of inferring prehistoric health from skeletal samples. Current Anthropology, 33, 343–70CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×