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AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 119:231–239 (2002)

Age Estimation From the Auricular Surface of the Ilium:


A Revised Method
J.L. Buckberry* and A.T. Chamberlain

Department of Archaeology and Prehistory, University of Sheffield, Sheffield S1 4ET, UK

KEY WORDS auricular surface; ilium; skeletal age at death; Spitalfields; forensic
anthropology; palaeodemography

ABSTRACT A revised method for estimating adult showed that the dispersion of age at death for a given
age at death using the auricular surface of the ilium has morphological stage was large, particularly after the first
been developed. It is based on the existing auricular sur- decade of adult life. Statistical analysis showed that the
face aging method of Lovejoy et al. ([1985] Am. J. Phys. age-related changes in auricular surface are not signifi-
Anthropol. 68:15–28), but the revised technique is easier cantly different for males and females. The scores from the
to apply, and has low levels of inter- and intraobserver revised method have a slightly higher correlation with age
error. The new method records age-related stages for dif- than do the Suchey-Brooks pubic symphysis stages. Con-
ferent features of the auricular surface, which are then sidering the higher survival rates of the auricular surface
combined to provide a composite score from which an compared with the pubic symphysis, this method promises
estimate of age at death is obtained. Blind tests of the to be useful for biological anthropology and forensic sci-
method were carried out on a known-age skeletal collec- ence. Am J Phys Anthropol 119:231–239, 2002.
tion from Christ Church, Spitalfields, London. These tests © 2002 Wiley-Liss, Inc.

The estimation of age at death of adult skeletal mirrored the age structure of the reference series
material is one of the more difficult tasks under- from which the methods were developed (Bocquet-
taken by physical anthropologists. Mays (1998, p. Appel and Masset, 1982), and did not allow for the
50) stated that “at present the lack of a wholly variation normal to a skeletal population (Suchey et
satisfactory technique for estimating age at death in al., 1986). When the Suchey-Brooks method (Brooks
adult skeletons from archaeological sites is one of and Suchey, 1990) was developed, this variation was
the most thorny problems facing human osteoar- made explicit by the documentation of the disper-
chaeology.” The problem arises from the fact that sion of age at death for each morphological stage of
rates of skeletal remodeling and degeneration, from the pubic symphysis.
which most methods of adult age estimation are The auricular surface method of age estimation
derived, can be highly variable between different has not been subject to the same levels of scrutiny as
individuals and populations.
pubic symphysis aging, and it is usually applied in
The life history of an individual will be an impor-
the form originally developed by Lovejoy et al.
tant determinant of the rate of skeletal aging. Fac-
tors such as endocrine status, diet, disease, physical (1985). Murray and Murray (1991) tested the auric-
activity, and cultural differences will contribute to ular surface method of Lovejoy et al. (1985) on a
the range of variation between males and females, sample of skeletons in the Terry Collection, to see
old and young, and rich and poor within a site, and how reliable the method was for use in forensic
also between populations from different sites cases. They found that the method was “unbiased
(Brothwell, 1981; Ubelaker, 1989; Schwartz, 1995; regarding race and sex” (Murray and Murray, 1991;
Hillson, 1996; Aykroyd et al., 1999). Even with a
similar biological background and environmental
Grant sponsor: Universities of Sheffield, York, and Leeds.
conditions, two individuals are likely to age at dif-
ferent rates. *Correspondence to: Miss Jo Buckberry, Research School of Archae-
Pubic symphysis age estimation was first applied ology and Archaeological Science, University of Sheffield, West Court,
to adult males (Todd, 1920), and was subsequently 2 Mappin St., Sheffield S1 4DT, UK.
redefined and tested, especially with regard to cre- E-mail: J.Buckberry@Sheffield.ac.uk
ating separate systems for females (Brooks, 1955;
Received 23 July 2001; accepted 17 April 2002.
Nemeskéri et al., 1960; Gilbert and McKern, 1973;
Suchey, 1979; Katz and Suchey, 1986; Brooks and DOI 10.1002/ajpa.10130
Suchey, 1990). These methods were found to gener- Published online in Wiley InterScience (www.interscience.wiley.
ate age distributions for different populations that com).

© 2002 WILEY-LISS, INC.


232 J.L. BUCKBERRY AND A.T. CHAMBERLAIN

p. 1166). However, they also found that the method ricular surface area of the ilium is more durable
consistently underestimated the age of older individ- than the fragile pubic symphysis, with higher levels
uals, and overestimated the age of younger individ- of survival and recovery, particularly in archaeo-
uals in their sample. They felt that this might have logical populations (Lovejoy et al., 1985; Waldron,
been attributable to differences in age structure be- 1987). However, the separate features of the auric-
tween the Todd Collection, on which the method was ular surface described by Lovejoy et al. (1985), such
developed, and the Terry Collection (Murray and as porosity, surface texture, and marginal changes,
Murray, 1991). Murray and Murray (1991) concluded appear to develop independently of each other. The
that the method was “too unreliable to be used as a age of onset for each stage of different features of the
single aging technique for forensic science purposes.” auricular surface appears to vary, and as a conse-
However, they conceded that the method would be quence the 5-year age categories of Lovejoy et al.
useful when used in conjunction with other methods
(1985) tend to overlap. Early-appearing features
of age estimation.
still present on the auricular surfaces of older indi-
The auricular surface method was also tested on
an archaeological sample of known age at death viduals were described by Lovejoy et al. (1985) as
from Belleville, Ontario (Saunders et al., 1992). The “residual.” The fact that this variation can occur
system was found to underestimate age at death within a single auricular surface indicates that the
especially for the older portion of the sample (over 45 method of Lovejoy et al. (1985) oversimplifies the
years), although it predicted the ages of younger changes seen, and that the 5-year intervals in their
adults reliably (Saunders et al., 1992). The authors scheme of age estimation may be optimistically nar-
found that estimates of age at death for many indi- row. This problem contributes to the difficulty found
viduals did not fall into the correct modal stages, with applying the method, as it leads to uncertainty,
indicating that the method of Lovejoy et al. (1985) and in some cases confusion, in assigning individual
may not allow adequately for individual variation in auricular surfaces to a particular age stage.
skeletal aging. It was also noted that intraobserver
error was high (19.3%) (Saunders et al., 1992), and A REVISED AURICULAR SURFACE METHOD
this may be due to the difficulty found in applying OF AGE ESTIMATION
the method, especially when classifying “ambiguous
specimens . . . that cannot with certainty be as- In view of these problems, we believe that the
signed to one age category” (Saunders et al., 1992, p. auricular surface age estimation technique would
99). benefit from the same level of reanalysis that has
Bedford et al. (1993) also tested the auricular sur- been undertaken for pubic symphyseal age estima-
face method on a sample of known-age skeletons tion. A quantitative scoring system, which examines
from the Grant Collection at the University of To- each different feature of the auricular surface inde-
ronto. As with other tests of the method, there was a pendently, should not only be easier to apply but will
tendency to overestimate ages of younger adults and also accommodate the overlap often seen between
to underestimate ages in categories above 60 years different stages. Our revised system has been devel-
old. oped from that of Lovejoy et al. (1985), and utilizes
AURICULAR SURFACE METHOD OF AGE their categories of age-related change seen on the
ESTIMATION OF LOVEJOY ET AL. (1985) auricular surface. The features used were trans-
verse organization, surface texture, microporosity,
The age-related changes seen on the auricular macroporosity, and changes in morphology of the
surface of the ilium were first described by Sashin apex and retroauricular area. Each of the features
(1930). He interpreted the changes seen in the ar- seen on the auricular surface was recorded indepen-
ticular cartilage of the joint as osteoarthritic, and dently and assigned a series of numerical scores
found that they were “progressive, and increase in corresponding to successive stages of degrees of ex-
extent and intensity with the age of the individual”
pression. Although one feature might be obscured by
(Sashin, 1930, p. 909). However, the regularity of
another, the use of standardized criteria (defined
these changes was not discussed. The age-related
below) allowed them to be assessed objectively. In
changes of the auricular surface were not exploited
as a method of estimating age at death until Lovejoy preliminary analyses, the retroauricular area was
et al. (1985) developed their technique. found to be a poor estimator of age, and this led to its
Lovejoy et al. (1985) described eight modal age exclusion from the revised method.
stages (typically encompassing 5 years), into which The surface is described using the same terminol-
each auricular surface could be placed using pri- ogy employed by Lovejoy et al. (1985). Figure 1
mary aging features. An age would then be esti- shows the locations used in describing the auricular
mated from within this modal stage, using secondary surface. Table 1 gives the descriptions of each loca-
indicators of age (apical activity and retroauricular tion, as defined in Buikstra and Ubelaker (1994).
activity). Each of the features of the auricular surface is de-
Auricular surface age estimation increased the scribed in detail, with a summary description of
range of methods that were available, and the au- each stage observed given in tabular form.
REVISED AURICULAR SURFACE AGING METHOD 233
TABLE 3. Scoring system for surface texture
Score Description
1 90% or more of surface is finely granular
2 50–89% of surface is finely granular; replacement of
finely granular bone by coarsely granular bone in
some areas; no dense bone is present
3 50% or more of surface is coarsely granular, but no
dense bone is present
4 Dense bone is present, but occupies less than 50% of
surface; this may be just one small nodule of dense
bone in very early stages
5 50% or more of surface is occupied by dense bone

TABLE 4. Scoring system for microporosity


Score Description
1 No microporosity is present
2 Microporosity is present on one demiface only
3 Microporosity is present on both demifaces

Fig. 1. Regions of the ilium used for auricular surface aging auricular surface is finely grained in early life, and
(redrawn after Lovejoy et al., 1985).
becoming more coarsely granular and densified in
older individuals. As with transverse organization,
TABLE 1. Definitions used to describe auricular surface this feature is scored in terms of what proportion of
(after Buikstra and Ubelaker, 1994)
the surface is covered by a particular type of texture.
Definition Description of locations Finely granular bone is defined as having grains
Apex Portion of auricular surface that predominantly less than 0.5 mm in diameter, and
articulates with posterior aspect of coarsely granular bone consists of grains predomi-
arcuate line nantly over 0.5 mm in diameter. Dense bone refers to
Superior demiface Portion of auricular area above apex surface appearance, rather than the amount of bone
Inferior demiface Portion of auricular area below apex
Retroauricular Region between auricular surface and present. It is defined as nodules or areas of bone
area posterior inferior iliac spine which are compact and smooth, with no surface
granularity. The scoring system for surface texture
is given in Table 3.
TABLE 2. Scoring system for transverse organization
Score Description Microporosity
1 90% or more of surface is transversely organized In the revised system, microporosity was defined
2 50–89% of surface is transversely organized as porosity of the surface (or perforations of sub-
3 25–49% of surface is transversely organized
4 Transverse organization is present on less than 25%
chondral bone), with the pores having a diameter of
of surface less than 1 mm. It is scored according to the presence
5 No transverse organization is present of microporosity on one or both of the two demifaces
of the auricular surface. Microporosity may be local-
ized or spread across large areas. Lovejoy et al.
Transverse organization
(1985) regarded microporosity as a secondary aging
Transverse organization refers to the horizontally feature. The scoring system for microporosity is
orientated billows and striae that run from the me- given in Table 4.
dial to the lateral margins of the auricular surface
Macroporosity
(Lovejoy et al., 1985). It was difficult to distinguish
between billows and striae and to be consistent in Macroporosity also perforates the surface of the
the recording of these features. Consequently, this bone. We define macroporosity as holes greater than
trait is scored in terms of what proportion of the 1 mm in diameter. Like microporosity, it may be
auricular surface is transversely organized. The pro- localized or spread across large areas. Lovejoy et al.
portion is estimated by eye, rather than measured, (1985) also considered macroporosity a secondary
and is assigned to 1 of 5 easily distinguishable aging feature. Macroporosity is scored according to
stages defined in terms of the percentage of surface its presence on one or both of the two demifaces of the
covered. The scoring system for transverse organi- auricular surface, in the same manner as for micro-
zation is given in Table 2. porosity. The scoring system for macroporosity is
given in Table 5.
Surface texture
Macroporosity should not be confused with corti-
This feature corresponds to that described as cal defects, which may be present at any age. Corti-
“grain” by Lovejoy et al. (1985). The texture of the cal defects are areas where the cortex of the bone is
234 J.L. BUCKBERRY AND A.T. CHAMBERLAIN
TABLE 5. Scoring system for macroporosity TABLE 8. Multiple regression of age against features
Score Description Unstandardized
Feature coefficients t P
1 No macroporosity is present
2 Macroporosity is present on one demiface only (constant) ⫺6.500 ⫺1.156 0.249
3 Macroporosity is present on both demifaces Transverse organization 4.316 2.527 0.012
Surface texture 7.105 4.115 ⬍0.001
Microporosity 5.572 3.680 ⬍0.001
TABLE 6. Scoring system for apical changes Macroporosity 4.669 2.720 0.007
Apical changes 3.282 2.675 0.008
Score Description
1 Apex is sharp and distinct; auricular surface may be
slightly raised relative to adjacent bone surface
2 Some lipping is present at apex, but shape of articular tographed were specifically chosen to illustrate the
margin is still distinct and smooth (shape of outline typical appearance seen at a particular age.
of surface at apex is a continuous arc)
3 Irregularity occurs in contours of articular surface; Blind test on a known-age sample
shape of apex is no longer a smooth arc
The new scoring system was then tested by one of
the authors (J.L.B.) on a known-age skeletal popu-
TABLE 7. Spearman correlations between age and feature for
auricular surface photographs of Bedford et al. (1989)
lation (n ⫽ 180) from Christ Church, Spitalfields,
London (held at the Natural History Museum, Lon-
Feature rs P don; Molleson and Cox, 1993), to assess how the
Transverse organization 0.942 ⬍0.01 features related to chronological age. Each auricular
Surface texture 0.930 ⬍0.01 surface in the collection was recorded twice, with an
Microporosity 0.654 ⬍0.01
Macroporosity 0.883 ⬍0.01
interval of 2 weeks between these analyses. Any
Apical changes 0.888 ⬍0.01 discrepancies between scores were noted, and if dis-
cordant, the surface was studied a third time. The
age and sex of the individual was not recorded on the
boxes, and care was taken that the observer did not
not complete. They are usually smooth-edged and do know this information prior to recording. While the
not cover a significant area of the auricular surface. sex of strongly dimorphic individuals would be ap-
Macroporosity may also be confused with areas of parent to the observer, it was not felt that this would
postmortem damage, which are usually sharp-edged cause bias, as the recording criteria were rigorous,
and irregular, often have paler colored bone around and applied solely to the auricular surface and not to
the edges, and may expose underlying trabecular the surrounding bone. The observer also avoided
bone that is always unremodelled. Care should be examining other parts of the skeleton, which may
taken in recording this feature, to ensure that no have given subjective clues to age at death. Color
confusion with postmortem damage has arisen. photographs were taken of every auricular surface.
Apical changes Once the study was completed, the photographs
were seriated for each feature, to check the consis-
The apex of the auricular surface can develop tency of the recording. The scores were then entered
small osteophytic growths, or lipping, which when into a computer database along with the docu-
more severe can alter the contour of the surface. This mented age and sex of each individual.
change was regarded as a secondary aging feature
by Lovejoy et al. (1985), and was described in terms RESULTS
of “activity.” The scoring system for apical changes is Although Kendall’s coefficient of concordance in-
given in Table 6. dicates a reasonable measurement of agreement
Preliminary testing among the five features (Wa ⫽ 0.691, P ⬍ 0.0005),
each feature supplies independent information
The new scoring system was initially applied to about age. This is seen in the results of a stepwise
archaeological skeletal material of unknown age at multiple regression, which indicates that all five
death from the Anglo-Norman site of Blackgate, features contribute to the prediction of age (Table 8),
Newcastle-upon-Tyne (n ⫽ 56; held at the Depart- and in the partial correlations between features af-
ment of Archaeology and Prehistory, University of ter controlling for the effect of age (Table 9). The
Sheffield), to test for ease of use and to check for partial correlations among the features are low and
reproducibility of results. The scoring system was mostly nonsignificant, confirming that the features
then applied to photographs of known-age auricular provide independent sources of information about
surfaces distributed by Bedford et al. (1989) that age.
accompany the system of Lovejoy et al. (1985), to see The combination of transverse organization, sur-
how well the individual features of the auricular face texture, microporosity, macroporosity, and api-
surface correlated with age (Table 7). Each feature cal changes was found to give the highest correlation
was found to have a high correlation with age, con- with age (rs ⫽ 0.609; P ⬍ 0.01). This “composite
sistent with the fact that the auricular surfaces pho- score,” calculated as the sum of the scores of the
REVISED AURICULAR SURFACE AGING METHOD 235
TABLE 9. Partial correlation coefficients between features TABLE 10. Independent two-tailed t-tests between males and
controlling for effects of age1 females for each composite score
TO ST MI MA AP Composite Age
score stage t df P
TO 0.381 0.136 0.217 0.040
ST ⬍0.001 0.138 0.316 0.169 5–6 I Sample size too small
MI 0.070 0.065 0.104 0.038 7–8 II ⫺0.331 4 0.757
MA 0.004 ⬍0.001 0.164 0.059 9–10 III ⫺1.825 20 0.083
AP 0.590 0.023 0.612 0.429 11–12 IV 0.373 30 0.711
13–14 V ⫺0.005 62 0.996
1
Coefficients above diagonal, p-values below, sample size n ⫽ 15–16 VI ⫺0.142 39 0.888
180. TO, transverse organization; ST, surface texture; MI, micro- 17–19 VII ⫺1.125 10 0.287
porosity; MA, macroporosity; AP, apical changes.

with age (Table 11). Although the r values are rela-


tively low, all were significant at the 99% confidence
level. The scores were combined to produce a com-
posite score, which increased the correlation with
age (males, rs ⫽ 0.624; females, rs ⫽ 0.626; P ⬍ 0.01).
Several composite scores were found to have sim-
ilar ranges, distributions, and mean ages. These
scores were grouped together to produce seven au-
ricular surface stages for the purposes of age esti-
mation. The age ranges, means, and median ages for
these stages are given in Table 12. It should be noted
that the mean age for auricular surface stage is
affected by the age structure of the reference sam-
ple, which in this case is biased toward older ages
(Bocquet-Appel and Masset, 1982; Jackes, 1992). To
compensate for this, a Bayesian analysis was under-
Fig. 2. Plot of composite auricular surface scores against age taken, using uniform priors following the method of
for Spitalfields sample. Spearman’s correlation coefficient of score Chamberlain (2000) to provide posterior probabili-
against age is given for males and females. ties of age, given the auricular surface stage (Table
13).
Reliability testing
separate features, was used in all subsequent sta-
tistical tests. The method was tested for intraobserver error by
A paired t-test was calculated for all individuals one of the authors (J.L.B.). Six well-preserved auric-
with both left and right auricular surfaces present. ular surfaces were recorded twice, at an interval of 2
The results showed no significant difference for the weeks. A paired t-test showed no significant varia-
composite score between the left and right sides (t ⫽ tion (P ⬎ 0.05) between the composite scores given
0.6; df ⫽ 157; P ⫽ 0.550). Subsequently, the left side on each occasion (t ⫽ ⫺1.348; df ⫽ 5; P ⫽ 0.235). A
was used for all analyses when both sides were different group of six auricular surfaces was tested
available, and the side available was used for all for interobserver error by graduate students in os-
other individuals. teology at the University of Sheffield and members
Previous analyses had revealed no significant dif- of the British Association of Biological Anthropology
ference in age-related changes of the auricular sur- and Osteoarchaeology. Cohen’s weighted kappa
face between males and females (Lovejoy et al., measure of agreement for ordinal data indicated a
1985; Murray and Murray, 1991). The ages were low level of interobserver error (␬ ⫽ 0.66) (Agresti,
plotted against composite scores for males and fe- 1988).
males as a scatter plot, with a regression line for The Spitalfields sample was also recorded using
both data sets (Fig. 2). The regression lines indicate the Suchey-Brooks pubic symphysis method, which
that there is little difference between sexes (males, was applied using the casts for males and females
rs ⫽ 0.624, P ⬍ 0.01; females, rs ⫽ 0.626, P ⬍ 0.01). (Suchey et al., 1988; Brooks and Suchey, 1990). The
A standard (two-sample, two-tailed) t-test was also pubic symphysis was only present for 58.9% of the
carried out to test for significant differences between sample. The rank order correlation between the six
males and females for each of the score categories. Suchey-Brooks stages and age is rs ⫽ 0.58; P ⬍ 0.01.
There were no significant differences between ages This compared favorably with the correlation be-
for males and females (P ⬎ 0.05; see Table 10). tween the new seven-stage auricular surface aging
A scatter plot of score against age for each feature, method and age (rs ⫽ 0.63; P ⬍ 0.01). This shows
shown in Figure 3, reveals wide variation in the age that although the Suchey-Brooks system is thought
of appearance of the features. A Spearman’s corre- to be the most reliable skeletal indicator of age
lation coefficient was calculated for each feature (Mays, 1998), the new auricular surface aging
236 J.L. BUCKBERRY AND A.T. CHAMBERLAIN

Fig. 3. Scatter plots of scores against


age at death in Spitalfields sample for each
of five features: transverse organization,
surface texture, microporosity, macroporos-
ity, and apical changes.

TABLE 11. Spearman’s correlation with age for each feature with other features into 5-year modal age stages.
and for composite score Our revised auricular surface method of age estima-
Feature rs P tion allows for a more realistic interpretation of the
changes. Although the age estimates produced by
Transverse organization 0.433 ⬍0.005
Surface texture 0.489 ⬍0.005 our method are wider, this revised method is easier
Apical changes 0.319 ⬍0.005 to apply and may be more reliable than that of
Microporosity 0.408 ⬍0.005 Lovejoy et al. (1985).
Macroporosity 0.533 ⬍0.005
Composite score 0.609 ⬍0.005 The sample size used to develop the method was
small (n ⫽ 180), with younger individuals underrep-
resented due to the age structure of the Spitalfields
Collection. The method outlined here needs to be
method has a higher correlation with age for the tested and redefined, using large, multiracial, and
Spitalfields sample.
known-age modern and, if possible, archaeological
DISCUSSION AND CONCLUSIONS populations. This will lead to the redefinition of age
ranges and standard deviations. Although Murray
Individual human skeletons show age-related
and Murray (1991) showed that the method of Love-
changes which progress at different rates. It would
joy et al. (1985) was equally applicable for different
appear that none of the current methods of skeletal
populations, this has not yet been demonstrated for
age estimation are able to provide age estimates
that are both precise (closeness of repeated mea- our revised method. Such a study is needed to de-
surements) and accurate (closeness to true value) termine if the method is universally applicable
(Sokal and Rohlf, 1995, p. 50), and that such precise across human populations, and will have important
levels of age estimation are unlikely to be developed implications for the applicability of the method to
in the foreseeable future. While precise age esti- archaeological samples.
mates are desirable and will always be sought, it is It has also been shown that there is no significant
not feasible to attempt to provide them if they are difference between sexes and sides. The lack of sys-
not a true reflection of the underlying biology. None tematic variation in the rate of aging between the
of the present age-estimation methods are able to sexes was surprising, but allows the same method
provide estimates within narrow age ranges, so con- and age estimates to be applied to both sexes, allow-
sequently age estimates need to be stated either as ing age to be assessed independently of sex.
broad ranges or as probability density functions The revised method generates scores that have a
(e.g., Jackes, 1992; Chamberlain, 2000). higher correlation with age than the Suchey-Brooks
Multiple regression shows that the features of the pubic symphysis system for the Spitalfields sample.
auricular surface age independently of each other, The age ranges produced by the revised auricular
indicating that each feature has to be interpreted surface method are similar to those given by Brooks
independently, rather than being grouped together and Suchey (1990), regarded as one of the most
REVISED AURICULAR SURFACE AGING METHOD 237
TABLE 12. Age estimates from composite scores and age stages
Composite score Auricular surface stage No. of specimens Mean age Standard deviation Median age Range
5–6 I 3 17.33 1.53 17 16–19
7–8 II 6 29.33 6.71 27 21–38
9–10 III 22 37.86 13.08 37 16–65
11–12 IV 32 51.41 14.47 52 29–81
13–14 V 64 59.94 12.95 62 29–88
15–16 VI 41 66.71 11.88 66 39–91
17–19 VII 12 72.25 12.73 73 53–92

TABLE 13. Posterior probability of age, given auricular surface sexes and potentially to different populations
stage, assuming uniform prior probability of age (Konigsberg and Frankenberg, 1992), and shows
Age I II III IV V VI VII older age-related changes than the pubic symphysis
15–24 0.86 0.33 0.27 0.00 0.00 0.00 0.00 (Lovejoy et al., 1985).
25–34 0.14 0.42 0.18 0.17 0.03 0.00 0.00
35–44 0.00 0.21 0.20 0.07 0.19 0.02 0.00
45–54 0.00 0.04 0.12 0.16 0.20 0.04 0.27 ACKNOWLEDGMENTS
55–64 0.00 0.00 0.07 0.20 0.18 0.11 0.00
65–74 0.00 0.00 0.02 0.14 0.26 0.10 0.24
75–84 0.00 0.00 0.04 0.20 0.07 0.27 0.49 We thank Dr. Louise Humphrey of the Natural
85–94 0.00 0.00 0.09 0.07 0.06 0.46 0.00 History Museum, London, for granting us access
to the Christ Church Spitalfields skeletal sample.
Comments by Dr. Humphrey and Dr. Pia Nystrom
important and reliable aging methods used at
of the Department of Archaeology and Prehistory,
present. This suggests that wide age estimates are
more realistic. Narrow age estimates will always University of Sheffield, on previous drafts of this
remain desirable, but by their nature do not allow paper and the suggestions made by anonymous
for the variation in age-related changes demon- referees are greatly appreciated. We also thank
strated by this study. By using narrower age esti- the osteology students and delegates of the British
mates, many individuals could be aged incorrectly, Association of Biological Anthropology and Osteo-
which may hinder identification in forensics cases. archaeology for taking part in the interobserver
This aging technique is important, because the error tests, and Alex Norman for drawing the il-
auricular surface is resistant to decay (Waldron, lustration. J.L.B. is currently funded by a White
1987), especially when compared with the fragile Rose Studentship from the Universities of Shef-
pubic symphysis. It is universally applicable to both field, York, and Leeds.

APPENDIX. Age and feature scores for known-age females (n ⫽ 94) and males (n ⫽ 86)
Age TO ST MI MA AP Age TO ST MI MA AP
Females 50 4 3 3 1 2
16 1 1 1 1 2 50 4 4 3 2 1
17 2 1 1 1 1 50 4 4 3 2 2
19 1 2 1 1 1 52 4 3 2 2 2
23 3 2 2 1 2 52 4 4 3 3 2
27 1 1 3 1 1 52 5 3 3 2 2
27 2 2 2 1 1 53 2 2 3 1 1
29 4 3 3 1 2 53 4 3 3 2 2
29 2 3 3 1 2 53 4 2 3 1 1
30 3 3 2 1 2 53 5 5 3 3 2
34 4 3 3 1 2 53 2 3 2 1 2
35 2 2 3 1 1 55 3 3 1 2 2
35 2 3 3 1 2 55 4 4 2 1 2
37 3 3 3 1 1 55 4 4 3 2 2
37 3 2 1 1 1 56 4 4 3 1 2
38 2 3 3 1 1 56 3 3 3 1 2
39 3 2 2 1 1 56 4 4 3 1 2
39 5 3 3 2 3 57 4 3 3 1 2
41 2 3 3 1 2 57 4 3 3 1 2
43 4 3 3 1 2 57 2 3 3 2 2
44 3 3 3 1 2 58 4 4 3 2 2
45 2 3 2 1 3 59 4 4 3 2 2
45 4 3 3 2 2 60 4 3 2 2 2
46 4 3 3 1 2 61 4 3 3 3 2
47 4 3 3 2 2 61 4 3 3 2 2
47 4 4 3 1 2 61 3 3 3 1 1
48 2 3 2 1 2 62 4 3 2 1 2
49 4 3 2 3 3 63 4 4 2 2 2
49 4 3 3 1 2 64 3 4 3 2 2
(continued)
238 J.L. BUCKBERRY AND A.T. CHAMBERLAIN
APPENDIX. Age and feature scores for known-age females (n ⫽ 94) and males (n ⫽ 86) (Continued)
Age TO ST MI MA AP Age TO ST MI MA AP
65 2 3 2 1 2 46 3 3 2 1 2
65 4 4 3 2 2 47 3 2 3 1 3
65 4 3 3 1 2 47 4 3 2 1 2
65 4 3 3 2 2 48 4 4 2 2 2
65 4 3 3 2 2 49 5 3 2 1 3
67 3 3 3 2 1 50 4 3 3 2 3
67 4 3 3 1 1 51 4 3 1 1 1
67 4 4 3 2 2 51 4 3 3 1 1
68 3 4 3 1 2 52 2 3 3 3 2
68 4 3 3 1 1 52 4 3 3 2 2
68 5 4 3 3 1 53 4 3 3 1 1
68 4 3 3 2 2 53 5 4 3 3 2
70 4 3 3 3 1 54 4 3 3 1 2
70 3 3 3 2 3 56 5 4 3 1 2
71 4 3 2 2 3 57 4 4 3 2 2
72 3 4 3 3 2 58 4 4 2 1 2
73 4 2 3 2 2 58 4 3 3 1 2
73 3 3 3 3 2 58 4 3 3 1 2
74 4 4 3 3 2 58 3 3 3 1 2
76 4 3 3 2 3 58 2 3 2 1 2
76 4 3 3 2 1 60 3 4 3 2 1
76 4 3 2 2 2 60 4 4 3 2 2
77 5 5 3 3 1 60 4 4 3 3 2
77 5 3 2 1 2 61 4 4 3 3 2
78 5 5 3 3 3 61 4 4 3 2 2
78 4 4 3 3 3 62 4 2 3 1 1
79 5 4 3 2 2 63 3 3 3 2 2
79 4 4 3 2 2 63 4 3 3 2 2
80 4 4 3 3 2 63 3 3 3 2 1
80 4 3 3 1 2 63 3 4 3 1 3
81 5 4 3 2 2 63 5 4 3 3 2
83 4 4 3 3 2 64 5 4 3 2 2
85 4 4 3 3 3 64 4 4 3 3 3
85 5 4 3 2 2 64 4 4 3 2 3
87 4 4 3 3 3 65 4 3 3 1 2
87 3 3 3 3 2 66 5 3 3 2 2
89 4 4 3 3 2 66 4 3 2 2 2
Males 66 4 4 3 1 3
16 2 2 1 1 3 67 4 3 3 1 2
18 4 3 1 1 1 67 5 4 3 2 2
21 2 3 1 1 1 68 4 3 3 3 2
22 3 3 2 1 1 68 5 5 3 3 2
25 2 3 1 1 2 69 4 4 3 1 2
26 2 1 3 1 1 69 5 4 3 3 2
27 3 2 1 1 2 69 3 4 3 2 2
32 3 3 3 1 2 70 4 3 3 1 3
32 4 3 3 2 2 70 4 3 3 2 2
32 5 3 2 1 2 70 4 3 3 2 2
34 2 2 2 1 2 71 5 3 3 3 1
34 3 3 2 1 1 71 4 3 3 1 2
34 4 2 3 1 2 71 4 4 3 2 2
34 4 3 2 1 1 72 4 4 3 2 3
36 3 2 3 1 1 72 4 3 3 2 2
36 2 3 1 1 2 75 3 3 3 2 2
37 2 4 3 1 2 76 2 3 3 1 3
38 2 2 2 1 1 77 4 3 1 1 2
39 2 2 3 1 2 78 5 4 3 2 2
39 2 3 3 1 1 79 4 3 3 3 2
39 4 3 3 1 2 81 3 3 3 1 2
40 4 3 2 1 1 88 4 3 3 1 2
44 2 3 3 1 1 91 4 4 3 1 3
45 5 3 3 2 1 92 4 4 3 3 3

Abbreviations as in Table 9.

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