Technical note: Error in Olivier and Pineau's regression formulae for calculation of stature and lunar age from radial diaphyseal length in forensic fetal remains

Stewart ([1979] Essentials of Forensic Anthropology, pp. 128–131) cites five regression formulae presented by Olivier and Pineau ([1960] Ann. Méd. Lég. 40:141–144) for estimation of fetal stature from diaphyseal length. Of these formulae, one appears problematic: the formula for calculation of stature from the radius yields values which suggest the fetus has a much greater crown-heel (CH) length than do the remaining formulae for the diaphyses of other long bones. Moreover, when this stature estimate, so derived, is then inserted into these authors' earlier general formula for estimation of lunar age (Olivier and Pineau [1958] Arch. Anat. 6:21–28) the error is compounded. A fetus is now indicated to be nearly a trimester older than when the CH lengths obtained by the other long bone formulae are used. Accordingly, we believe this particular formula, unlike the others, is incorrect and should not be used to estimate lunar age from fetal remains. © 1996 Wiley-Liss, Inc.     

An elusive paleodemography? A comparison of two methods for estimating the adult age distribution of deaths at late Classic Copan,Honduras

Comparison of different adult age estimation methods on the same skeletal sample with unknown ages could forward paleodemographic inference, while researchers sort out various controversies. The original aging method for the auricular surface (Lovejoy et al., 1985a) assigned an age estimation based on several separate characteristics. Researchers have found this original method hard to apply. It is usually forgotten that before assigning an age, there was a seriation, an ordering of all available individuals from youngest to oldest. Thus, age estimation reflected the place of an individual within its sample. A recent article (Buckberry and Chamberlain, 2002) proposed a revised method that scores theses various characteristics into age stages, which can then be used with a Bayesian method to estimate an adult age distribution for the sample. Both methods were applied to the adult auricular surfaces of a Pre-Columbian Maya skeletal population from Copan, Honduras and resulted in age distributions with significant numbers of older adults. However, contrary to the usual paleodemographic distribution, one Bayesian estimation based on uniform prior probabilities yielded a population with 57% of the ages at death over 65, while another based on a high mortality life table still had 12% of the individuals aged over 75 years. The seriation method yielded an age distribution more similar to that known from preindustrial historical situations, without excessive longevity of adults. Paleodemography must still wrestle with its elusive goal of accurate adult age estimation from skeletons, a necessary base for demographic study of past populations.     

Lead exposure in italy: 800 BC-700 AD

Certain social and industrial activities that were common among Imperial Age Romans have been suggested to have caused lead poisoning whose sociological consequences may have afflicted many members of the aristocratic social stratum. Evaluation of this suggestion has awaited quantitative data. This study reports the skeletal lead content of twenty Italian archaeological populations. Imperial Age populations demonstrated up to ten-fold more bone lead than their predecessors or successors.     

Age estimation from dental eruption in infant and juvenile baboons (Papio sp.)

Two regression methods are proposed for estimating age in nonhuman primates from deciduous dental eruption data. The first method consists of step-wise multiple regression using dental eruption state (present/absent) of each tooth as independent variables. The second method uses the total number of teeth erupted as an independent variable in an exponential model. We applied both methods to a sample of 175 well nourished infant and juvenile baboons (Papio sp.), housed in an outdoor breeding corral, and ranging in age from birth to 763 days. From this sample, 129 animals were used to compute the regression formulae, and 46 animals were used for cross validation. Both models show good overall fits and high predictive accuracy with the independent cross validation sample.     

Changes in life-cycle strategies of Carabus problematicus over a range of altitudes in Northern England

ABSTRACT.

• 1 Mandible tip length has been used to estimate the age of individual C.problematicus Herbst caught over an altitude range of more than 700 m in northern England.
• 2 At 100 m the great majority of females laid eggs in the summer of their emergence as adults. The female life-cycle is predominantly annual and 24% only of the egg-bearing individuals were in their second year.
• 3 Above 250 m, most females did not reproduce until the summer of the year following emergence, giving a biennial life-cycle. 96% of egg-bearing females caught above 830 m were in their second year.
• 4 All the males caught during the breeding season at 100 m had emerged within that calendar year and it is concluded that the male life-cycle is annual at this altitude.
• 5 Above 250 m, 83% of the males caught during the breeding season were in their first calendar year, suggesting that recently emerged males may inseminate second year females and also that the male life-cycle is predominantly annual over the whole altitude range studied.
• 6 At the higher temperatures of the lowland site females not only produce eggs in the year of emergence, they also produce more eggs per individual than at the higher sites. Egg production depends on food intake which involves mandible wear and individuals at the lowland site have significantly higher rate of mandible wear than at the sites above 250 m.

     

Skeletal and dental growth and development in chimpanzees of the Taï National Park, Côte D'Ivoire

An extraordinary collection of 22 immature skeletons from Taï National Park, Côte d'Ivoire, has provided a rare opportunity to establish the timing of dental eruption and its correlation with skeletal fusion and morphometrics in wild chimpanzees of known chronological ages. Comparison of the immature Taï chimpanzees Pan troglodytes verus with adults from the same population show that sex differences in skeletal maturation apparently appear during the Juvenile II stage, about age 8. A few skeletons from other chimpanzee field sites conform to the dental and skeletal growth in Taï chimpanzees. The tempo of wild chimpanzee growth contrasts sharply with the rate demonstrated for captive individuals. Captive chimpanzees may mature as much as 3 years earlier. The ability to link physical development with field observations of immature chimpanzees increases our understanding of their life-history stages. These data provide an improved dataset for comparing the rates of growth among chimpanzees, Homo sapiens and fossil hominids.     

On estimating mortalities from osteological age data

A statistical method (based on the maximum likelihood principle) for estimating mortalities of skeletal populations is presented. The method can be applied both when osteological age groups are not overlapping as well as when they are. The results are presented as point estimates and as confidence intervals around these. The method is applied to two series from the Middle Ages: Westerhus and Helgeandsholmen.