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determine sex with a high degree of accuracy (Bass 1987). The sexual
dimorphism of the pelvis is primarily the result of reproductive mechanics, and is
not readily apparent until adolescence. Beginning in adolescence, the female
pelvis expands relative to its height, while the male pelvis continues along
trajectories established at birth (Buikstra and Ubelaker 1994:16). Holcomb and
Konigsberg (1995:113) have reported a greater than 66 percent accuracy utilizing
the greater sciatic notch of the ilium to determine the sex of known infant
skeletons, and these authors have suggested that genetic morphological traits
such as these may offer further avenues of research for the sexing of immature
skeletons.
Adolescent characters can begin to develop as early as nine years of age.
Detection of female aspects in a very young os coxae would indicate a high
probability of accuracy (Coleman 1969). Conversely, male patterns observed in
an adolescent os coxae are to be considered inconclusive, as the remains may
represent a female as yet undeveloped (Buikstra and Ubelaker 1994:16). In
such cases, additional corroborative evidence must be sought to make a firm
determination of sex. In addition, male crania may retain a gracile, female form
during early adolescence. Hence, detection of male characters in adolescent
skeletal material is suggestive of its masculinity (Buikstra and Ubelaker 1994:16).
Other metrically dimorphic attributes include the maximum diameter of the femur
head and the maximum facial breadth (Buikstra and Ubelaker 1994:16). This
form of variation is often continuous in nature, with males being longer or larger
than females. Discriminant function formulae are used to segregate individuals
based upon patterns of sexually dimorphic growth and musculature (e.g., Snow
et al. 1978; Stewart 1979; Richman et al. 1979; Kelley 1979; Steele 1980). The
formulae are typically applied with the most success to the long bones. Muscular
development is also sometimes evaluated through these formulae, but accurate
measurement of such development is problematic (Workshop of European
Anthropologists 1980; Brothwell 1981; Isan and Miller-Shaivitz 1984; St.Hoyme
and Isan 1989).
An abbreviated listing of the metrical and morphological characters utilized in
sexing the skeletal material is presented in Table 2. A complete list of all
characters recorded and the organization of analytic methods is presented in
Appendix A (Stewart 1979; Brothwell 1981; Isan and Loth 1986; Isan and
Miller-Shaivitz 1986; Bass 1987; Bennett 1988; Ubelaker 1989).
Estimation of Age at Death
The determination of age relies on the assessment of the physiological age of the
skeleton, as opposed to the chronological age of the individual.
The
physiological age is based upon relative growth patterns, and is hoped to give an
accurate estimate of chronological age, but environmental, nutritional, and
disease stresses often cause changes in the skeleton which will mask the true
age of the individual. In addition, the accuracy with which age can be estimated
varies inversely with the age of the individual at death. In younger years, with
age being estimated primarily upon observed developmental changes, more
precise estimates are possible, whereas in older individuals, age estimates are
more often accomplished via the observation of degenerative changes, which
offer less accuracy.
Age determination can be accomplished through many means, and a holistic
analysis of all possible age-related attributes is best for an overall estimate.
Some of the more typically utilized attributes include:
1.
2.
3.
4.
5.
6.
7.
8.