A New Method To Estimate Adult Age-at-Death Using The Acetabulum
A New Method To Estimate Adult Age-at-Death Using The Acetabulum
KEY WORDS bioarchaeology; forensic anthropology; age estimation; stepwise multiple regression
ABSTRACT Rissech et al. (J Forensic Sci 51 (2006) descriptions of age categories instead of photos. Three stat-
213–229) described a method to estimate age-at-death of istically significant characteristics highly correlated with
adult males using seven traits of the fused acetabulum. age (P < 0.05) are capable of estimating age-at-death with
This study simplifies Rissech et al.’s technique and extends 81% accuracy, both sexes combined. For misidentified indi-
its application to adult females. Rissech et al.’s original viduals the tendency was to underestimate age. Results of
scoring method was applied to a sample of 100 known-aged both intraobserver error testing and inter-rater reliability
adults, three variables were selected based on stepwise demonstrated a moderate to substantial agreement in scor-
multiple regression, and ages were collapsed into three ing between observers. When estimating the degree of de-
broad ranges: young adult (17–39 years), middle adult (40– velopment of features osteophyte development of the ace-
64 years), and old adult (651 years). The revised method tabular rim was the most inconsistent between observers.
was applied to 249 new known-aged individuals from two The revised acetabular method shows promise in estimat-
other samples. To minimize observer bias, highlight the ing age for adults, particularly for those over the age of 65
most critical traits, and encompass more age-related varia- years. Am J Phys Anthropol 000:000–000, 2012. V 2012
C
Estimating age-at-death with accuracy is important in England. Using a Bayesian calculation procedure for de-
bioarchaeological and forensic investigations because it velopmental stages of seven age-related traits of the
is a component of both (1) the biological profile, which fused acetabulum, Rissech’s work produced encouraging
establishes the basic physical identity of a person, results in distinguishing stages within the senior age
including sex, stature, and ancestral background and (2) category. Because estimating the age of those over 60
the demographic profile, which helps to form the sample years is notoriously difficult for many morphological age
age distribution. It is well known that activity, genetics, estimation techniques, degeneration of the acetabulum
health, and overall lifestyle affect the rates at which has a valuable role to play in the identification of the
age-related changes are expressed in the skeleton (Is _ can, elderly. Stull and James (2010) recently evaluated
1989; Boldsen et al., 2002). Because individual growth Rougé-Maillart et al.’s (2004) original aging criteria and
rates vary, age-at-death is always reported as a range. found that although acetabular features demonstrate the
To account for variation in the aging process, continual capability to estimate age, an improved coding system
testing of skeletal age-at-death techniques is essential. and percent correct classification approach is necessary
One area of the skeleton that has frequently been used to determine accuracy and precision.
for aging adults is the os coxae. Methods using the auric- Further to the work by Stull and James (2010), a pre-
ular surface and pubic symphysis are both well docu- liminary study was conducted (Calce and Rogers, 2011)
mented (Lovejoy et al., 1985; Suchey and Katz, 1998; to test Rissech et al.’s (2006) adult age estimation
Buckberry and Chamberlain, 2002) and employed often method using the acetabulum on a sample (n 5 100) of
in skeletal aging. Recently, another area of the os coxae, males from the Grant Collection (GRO) housed at the
the acetabulum, has shown promise as an effective age University of Toronto. The objective of such preliminary
indicator (Rissech et al., 2006; Rougé-Maillart et al., research by the current author was to determine the ac-
2007; Stull and James, 2010). Due in part to its postde- curacy and repeatability of several aging criteria pro-
positional preservation in comparison to other osseous posed by Rissech et al. (2006) on a North American pop-
regions, acetabular patterns of observable degeneration ulation. Three main problems were identified. First, that
were first reported in 2004 by Rougé-Maillart et al. who the statistical software program associated with Ris-
identified four potentially age-related skeletal features:
the acetabular rim, the acetabular fossa, the lunate sur-
face, and apical activity. Rougé-Maillart et al. (2004) pro-
posed that these acetabular aging traits complemented
*Correspondence to: Stephanie Calce, Department of Anthropol-
Lovejoy et al.’s (1985) auricular surface technique to esti- ogy, University of Victoria, P.O. Box 3050, STN CSC, Victoria, BC,
mate age, both of which were tested by Rougé-Maillart Canada V8W 3P5. E-mail: scalce@uvic.ca
on a small modern sample of known age European males
(n 5 30) from Spain and France. The high correlation Received 17 February 2011; accepted 28 December 2011
between osseous changes and age-at-death led to further
research (Rissech et al., 2006, 2007) on a larger Euro- DOI 10.1002/ajpa.22026
pean sample (n 5 394) of adult males from 18th to 20th Published online in Wiley Online Library
century cemetery collections in Portugal, Spain, and (wileyonlinelibrary.com).
C 2012
V WILEY PERIODICALS, INC.
2 S.E. CALCE
Fig. 2. Orientation image for Variable 1, acetabular groove. To evaluate, hold the os coxae in anterio-lateral aspect and flip hori-
zontally. The acetabular rim should be viewed close-up, under a light source, and at eye level. The area of inspection includes the
lunate surface where it meets the rim, as denoted by the dotted line.
Specimens were selected from each of the GRO and tions of age were established: young adult (17–39 years),
UTen collections based on the number of usable skele- middle adult (40–64 years), and old adult (651 years).
tons (Table 1). The GRO and UTen were appropriate col- Variable descriptions for each broad category of age form
lections to evaluate the usefulness of acetabular criteria the new revised method by the author to estimate age-
to estimate age-at-death because they are made up of an at-death from the acetabulum (Figs. 2–6). Figures 2 and
adequate number of male (n 5 147) and female (n 5 87) 3 demonstrate: [1] how the os coxa was oriented for
specimens (Bedford et al., 1993; UTen Forensic Anthro- inspection of variables and [2] point to anatomical loca-
pology Centre, 2005). Seriation of the male GRO and tions where age-related characteristics were observed.
female UTen samples revealed similar age-related Figures 4–6 were used to estimate age for an unknown
changes at the acetabular rim, the anterior inferior iliac individual. Left os coxae were examined, with the right
spine, and at the apex of the posterior horn of the lunate being substituted if poor preservation precluded analysis
surface. Based on trait expression observed within the of the left. The acetabulum was morphologically
GRO and UTen collections of individuals, broad defini- inspected, focusing on the total pattern of observable
Fig. 3. Orientation image for Variables 2 and 3, osteophyte development of the acetabular rim, and apex growth. To examine
age-related characteristics, hold os coxae in anterio-lateral position. An adequate light source is favorable to distinguish features of
age-related morphological variation. Areas of examination include the superior portion of the lunate surface below the anterior infe-
rior iliac spine, and the posterior horn of the lunate surface, also known as the apex.
traits to determine whether the individual expressed Testing the revised method
similarities associated with either the young, middle, or
older age phase. Based on analogous expressions of The revised method was tested blind on two contempo-
young, middle, or older age qualities (Figs. 4–6), age-at- rary North American skeletal populations (n 5 249). The
death was estimated by reporting a range, 17–39 years, UTen collection (N 5 650), housed at the University of
40–64 years, or 651 years. Tennessee Forensic Anthropology Research Center, con-
Fig. 4. Line drawings and associated descriptions of Variables 1, 2, and 3 for the young adult age category, 17–39 years. To
assess age of an unknown individual, morphologically inspect the acetabulum and focus on the total pattern of observable traits to
determine whether the individual expresses similarities associated with the young adult age phase. Based on analogous expressions
of young adult age qualities, estimate age-at-death by reporting a range, 17–39 years.
Fig. 5. Line drawings and associated descriptions of Variables 1, 2, and 3 for the middle adult age category, 40–64 years. Mor-
phologically inspect the acetabulum and focus on the total pattern of observable traits to determine whether the individual
expresses similarities associated with the middle adult age phase. Based on analogous expressions of middle adult age qualities,
estimate age-at-death by reporting a range, 40–64 years.
tains donated complete skeletons predominantly made Males were tested using both the UTen and UNM
up of European-derived (White) or African-derived documented collections. Because the test for females was
(Black) persons (UTen Forensic Anthropology Centre, developed on the UTen sample, age estimation of female
2005). The UNM Documented Collection, housed at the specimens was tested on individuals belonging only to
Maxwell Museum of Anthropology at the UNM (N 5 the UNM collection. The samples were chosen on the ba-
257), contains complete skeletons from donated persons sis of high-quality preservation of skeletal elements;
and positively identified forensic cases with documented however, of 100 female and 200 male ossa coxae only 60
demographic information, representing diverse socioeco- and 189 respectively were in a condition suitable for
nomic classes and ethnic affinities (Komar and Lathrop, evaluation. In total, 51 specimens were not evaluated
2006). Age-at-death is known for 77% of individuals (n 5 because they were either: poorly preserved; altered by
698), and 79% of persons (n 5 716) are over 40 years of surgical implant at the site of the acetabular–joint; miss-
age; both robust samples, the UTen and UNM collections ing from storage box; or damaged at the rim /apex due
are appropriate models to test age estimation for older to mishandling. Eighty-five individuals were tested from
adults (UNM Maxwell Museum of Anthropology, 2003; the UTen Collection, 164 from the UNM Collection. They
UTen Forensic Anthropology Centre, 2005; Komar and range in age from 19 to 101 years, and died between
Lathrop, 2006; Grivas and Komar, 2008). 1984 and 2006 (UNM Maxwell Museum of Anthropology,
Fig. 6. Line drawings and associated descriptions of variables 1, 2, and 3 for the old adult age category, 651 years. Morphologi-
cally inspect the acetabulum and focus on the total pattern of observable traits to determine whether the individual expresses simi-
larities associated with the older adult age phase. Based on analogous expressions of older adult age qualities, estimate age-at-
death by reporting a range, 651 years.
2003; UTen Forensic Anthropology Centre, 2005). Sam- or true value) was calculated by dividing the number of
ple sizes are displayed in Table 1, and the age distribu- correct calculations by the total number of specimens. To
tion of the sample is presented in Figure 7. test for intraobserver error, 45 individuals were selected
Specimens were chosen randomly from each age cate- from the UTen and UNM samples (UTen males, n 5 25;
gory but resulted in a test population made up of largely UNM females, n 5 20) and subjected to re-examination
‘‘American Whites’’ (n 5 207, males and females com- by the author (Table 1). Intraobserver error was calcu-
bined). Asian descent is not represented in this sample lated by the difference in categorical assignment
and ‘‘American Blacks’’ only make up 7% of the total between the first and second age estimates. To quantify
sample population, whereas ‘‘Hispanic’’ persons are rep- interobserver constancy and evaluate the utility of ace-
resented by 6%. Of the 249 individuals studied, 11 per- tabular descriptions with associated line drawings, 55
sons were not identified as belonging to any ancestral ossa coxae were observed under identical conditions by
group; reasons for this may include failure to collect rele- three additional independent observers with varied
vant information on intake of body donation. Males and osteological experience.
females were examined separately to identify sex-specific An inter-rater reliability analysis using the weighted
differences or problems with the technique. Individuals Kappa statistic was performed to determine consistency
with noninflammatory osteoarthritis were not excluded among raters (Fleiss and Cohen, 1973; Landis and Koch,
because such manifestations are related to age and/or ac- 1977). Kappa assesses the proportion of agreement
tivity. Known ages for each individual were not docu- between observers corrected for chance and the standard
mented until each specimen was examined, to eliminate measure of interobserver reliability with nominal data
observer bias. If the individual’s known age fell within (e.g., young, middle, and old). Scaled on a range from 21
the estimated age class (young, middle, or old), the age- to 11, a negative kappa value indicates a poorer than
at-death calculation was recorded as correct. A measure chance agreement, zero indicates agreement totally
of accuracy (how close a measured value is to the actual by chance alone, a positive value indicates a better than
chance agreement, and 11 indicates perfect agreement
(Fleiss and Cohen, 1973; Walrath et al., 2004). Kappa
does not take into account the degree of disagreement
between observers and all disagreement is treated
equally as total disagreement. Therefore when the cate-
gories are ordered, it is preferable to use weighted
Kappa, and assign different weights wi to subjects for
whom the raters differ by i categories, so that different
levels of agreement can contribute to the value of Kappa.
Based on the assessment criteria of Landis and Koch
(1977) for the adequacy of Kappa, a weighted Kappa
score of 0.41–0.60 indicated a ‘‘moderate agreement,’’
and 0.61–0.79 was used as an indicator of ‘‘substantial
agreement’’ between observers for all traits to estimate
age (Landis and Koch, 1977). The Intraclass Correlation
Coefficient (ICC) was used to measure the reliability of
ratings and absolute agreement between three observers
Fig. 7. The sample age distribution for both UTen and UNM (Shrout and Fleiss, 1979). ICC is useful when two or
collections of individuals (males and females combined) based
more raters are used to rate the same study subjects; in
on known chronological ages. Across all age classes, age was
estimated for 249 persons. Fewer numbers of individuals are this study, the measurement of absolute agreement is
represented by the young adult age category, likely because valid because systematic differences are relevant to
older aged persons have an increased susceptibility to mortality. show consistencies (or irregularities) in scoring (Bartko,
A bell shaped curve symmetrical about the mean (60.5 years) 1976). ICC ranges from 21 to 11 where 11 indicates
represents the frequency distribution of the test population dis- identical ratings for a subject, or perfect agreement.
played in 10-year age classes; the sample population is normally Four separate scores for weighted Kappa and ICC were
distributed. Above each bar, the number of individuals in each generated to assess interobserver reliability: (1) the over-
10-year age class (n) is also reported. all ability to estimate age-at-death based on the combi-
TABLE 2. Results of stepwise-multiple-regression for seven variables as defined by Rissech et al. (2006)
Standard R2 R2 other Probability Pct change
In Variable coefficient increment X’s T-Value level Sqrt (MSE)
Yes v1 (groove) 0.2523 0.041516 0.348036 2.6006 0.010776 2.9279
Yes v3 (rim porosity) 0.2790 0.036181 0.535084 2.4278 0.017056 2.4916
Yes v4 (apex activity) 0.2444 0.037373 0.374115 2.4674 0.015379 2.5893
No v2 (rim shape) 0.004172 0.659325 0.8231 0.412540 0.1684
No v5 (outer edge of fossa) 0.002102 0.309018 0.5831 0.561199 0.3455
No v6 (fossa activity) 0.004254 0.256713 0.8311 0.408011 0.1615
No v7 (fossa porosity) 0.005560 0.340952 0.9513 0.343878 0.0496
TABLE 4. Interobserver reliability using the Intraclass Correlation Coefficient (ICC) (P < 0.001) for (1) the overall age-at-death esti-
mate and (2) for each individually assessed trait
# of subjects # of raters Single measure of ICCa 95% confidence interval
Age-at-death estimate 55 3 0.701 0.569–0.796
Trait 1 (acetabular groove) 55 3 0.725 0.583–0.826
Trait 2 (osteophyte development at rim) 55 3 0.543 0.388–0.681
Trait 3 (apex growth) 55 3 0.760 0.654–0.843
a
Intraclass correlation coefficient, ICC: 0.5–0.6 5 moderate agreement; 0.7–0.8 5 strong agreement; and [0.8 5 almost perfect
agreement (Portney and Watkins, 2000).
nation of three observable traits, i.e., which individuals bles (Figs. 2–6). Forty-three out of 45 individuals were
were classified as young, middle, or old adults and (2) aged the same when subjected to re-examination by the
how each of the three individual traits (acetabular author (error in scoring 5 4.4%). When estimating age,
groove, osteophyte development of the acetabular rim, the average inter-rater reliability was Kappa 5 0.569
and apical growth) were scored by independent observers (95% CI 0.407–0.732, SE 0.08) and ICC 5 0.701 (95% CI
as being young, middle or old. 0.569–0.796), indicating a moderate to substantial agree-
Box plots, Spearman’s Rank correlation, and the Krus- ment between observers (Tables 3 and 4). Despite their
kal–Wallis test were used to compare and analyze popu- varied osteological experience, observers were able to
lation distributions between young, middle, and older identify acetabular variables consistently and use them
age categories to detect differences and associations to accurately estimate age. Among all traits, apical activ-
between trait expression and known chronological age. ity was the easiest to differentiate (Kappa 5 0.660; ICC
Statistical analyses were performed using SPSS for Win- 5 0.905); osteophyte development of the acetabular rim
dows release 19.0.0 (1 August 2010) and MedCalc for proved the most difficult (K 5 0.424; ICC 5 0.780;
Windows, version 11.6.1.0 (MedCalc Software, Maria- Tables 3 and 4). Age dependence of individual traits is
kerke, Belgium). presented in Table 5 where the correlation between esti-
mated trait scoring and actual age is given by three
RESULTS independent observers. Experience of the observer and
familiarity with defined character traits can improve
Stepwise multiple regression analysis of data using interobserver reliability. Results of both intra- and inter-
Rissech et al.’s (2006) original variables on 100 male observer error testing demonstrate a reasonable degree
skeletons from the GRO (Calce and Rogers, 2011) indi- of reproducibility indicating that only a modest amount
cates that there are three statistically significant varia- of error exists when estimating the degree of develop-
bles highly correlated with age: Variable 1, acetabular ment of features. Investigators should be aware that del-
groove (P-value 0.01); Variable 3, acetabular rim porosity icate features of the acetabulum are more difficult to dis-
(P-value 0.017); and Variable 4, apex activity (P-value tinguish on greasy bone, and specimens may appear
0.015). Note that Variable 3, as defined by Rissech et al. younger in these cases.
(2006) becomes Variable 2 (osteophyte development Males (n 5 189) and females (n 5 60) were examined
of the acetabular rim) in the revised method. R2 and separately; no significant sex-specific differences were
P-value coefficients for data collected on the GRO for found. In this early stage, it appears the method is not
each of Rissech et al.’s (2006) seven variables are pro- dependent on sex, although further testing on a larger
vided in Table 2. female sample is favorable to support these preliminary
results. The three traits identified in this analysis are
Testing the revised method highly correlated with age (P \ 0.05), and together are
capable of estimating age-at-death with 81% accuracy,
Each observer was able to score traits effectively using both sexes combined. Of the percentage wrong (19%),
only the information given in the descriptions of varia- the tendency was to underestimate age by one age cate-
age related traits is propitious, so far, methods using the TABLE 8. Sample age distribution for males and females
acetabulum to estimate age have not employed Bayes’ in the UTen and UNM collections
theorem to correct this problem.
Age class Males (n) Females (n)
A component system was not used because numerical
scoring of qualitative variables requires more rigid 16–20 2 0
descriptions of progressive biological phenomena (Meindl 21–30 8 2
et al., 1985). Component scoring systems fail to capture 31–40 23 2
age-related variability and can be problematic if the in- 41–50 31 3
51–60 42 8
vestigator does not understand descriptions distinguish- 61–70 34 13
ing key features. For example, differentiating between 71–80 28 15
what classifies a trait as ‘‘1’’ from ‘‘2’’ or ‘‘2’’ from ‘‘3,’’ etc. 81–90 18 12
For these reasons, biological assessment is based on a 91–99 3 4
basic sequence of modal changes that allows for full inte- 100–109 0 1
gration of all age-related variables and reduces intra- TOTAL 189 60
and interobserver error (Lovejoy et al., 1985; Brooks and Young adult (19–39) 30 4
Suchey, 1990; Meindl et al., 1990). To employ the Middle adult (40–64) 91 14
author’s new method effectively, all three traits of the Old adult (651) 68 42
TOTAL 189 60
acetabulum for each individual must be in good condi-
tion for evaluation: that is, not altered by surgical
implant at the site of the acetabular–joint or damaged at
the rim /apex. Additional research is necessary to deter- the smallest number of individuals belong to this age
mine which trait (1, 2, or 3) is most accurate to estimate category (n 5 34; Table 6), but may also reflect less vari-
age in adult samples. For now, investigators should ation and absolute change to pristine morphology com-
examine the total pattern of observable traits and select monly observed in early adulthood. Larger error was
the age category that most closely resembles the acetab- observed for middle and older aged adults (17% and 22%
ular region of the unknown specimen (Lovejoy et al., respectively). The author considers two explanations for
1985; Meindl et al., 1990; Suchey and Katz, 1998; Rog- this result. First, large inaccuracies are merely a statis-
ers, 2009). For use with ordinal categorical variables, tical artifact of the sample, because the largest propor-
modal phase analysis is favorable over the more compli- tion of UTen and UNM individuals for whom age was
cated component scoring system because it incorporates estimated (86% of total sample) belong to these age
both early and late phases of development into one age classes (Tables 6 and 8). Second, age-related morphologi-
class (Rogers, 2009). A more robust age class, as is used cal changes are highly variable for individuals 401
in this study, is necessary to provide a more accurate years, where further research into specific degenerative
representation of the variation associated with acetabu- modifications targeting middle-aged and elderly persons
lar morphology (Franklin, 2010). Doing so in a forensic is required (Calce and Rogers, 2011).
context avoids excluding decedents based on chronologi- Issues of donor-based and forensic skeletal collections
cal age and instead, preserves attributes of physiology are a current topic of debate in physical anthropology.
(Suchey and Katz, 1998; Cunha et al., 2009). In compari- Multiple biases of sample distributions must be consid-
son to the pubic symphyseal and auricular surface aging ered to determine whether these populations are repre-
methods, the acetabulum technique performs better at sentative of normal variation both in living and decedent
reducing broad categories of age for estimates of groups (Usher, 2002; Grivas and Komar, 2008). The
unknown individuals, particularly for those over 50 research design of this project focused on maximizing
years (Suchey and Katz, 1998; Buckberry and Chamber- the sample size to include as many usable specimens as
lain, 2002). Unlike other areas of the skeleton, continued was possible. With respect to sex ratio, males are overre-
age-related changes are observed in the acetabulum presented in the test sample accounting for 76% of all
beyond the sixth decade; ‘‘the acetabulum in the future, age estimates. Due to the limited number of females
may in the end be the most reliable for 60-year-old or comprised in the entire UNM collection (38.2%), this
older individuals’’ (Cunha et al., 2009: 5). The next (and result is not considered unusual (Grivas and Komar,
ongoing) step of this research is to develop more narrow 2008). Although no significant sex-specific differences
age categories from morphological descriptions particu- were found, the sample of female specimens used in this
larly for individuals over 65 years. investigation was small and should be increased. The
author suggests expanding the research to focus more
Directions for future research specifically on the female expression of age-related ace-
tabular traits to determine whether differences in carry-
Assignment to an incorrect age group was low (19% ing capacity at the femoroacetabular joint produce vari-
across all age classes; Table 6). Percentage wrong esti- able morphology between sexes.
mates for each age category varied with the smallest Although the number of individuals in the middle and
error occurring for younger persons (15%), likely because older age categories are consistent (Table 8), younger
adults (17–39 years) are underrepresented (n 5 34, 14% tons. In: Hoppa RD, Vaupel JW, editors. Paleodemography:
of total sample; Table 6). As a person ages, they become age distributions from skeletal samples. Cambridge: Cam-
more susceptible to mortality which explains the large bridge University Press. p 73–106.
number of individuals in the documented UTen and Brooks SP, Suchey JM. 1990. Skeletal age determination based
on the os pubis: a comparison of the Ascádi–Nemeskéri and
UNM skeletal collections over 40 years of age, resulting
Suchey–Brooks methods. J Hum Evol 5:227–238.
in an inevitably smaller sample size for persons less Buckberry JL, Chamberlain AT. 2002. Age estimation from the
than 39 years. Even though the sample size for young auricular surface of the ilium: a revised method. Am J Phys
adults (males and females combined) is not as sizeable Anthropol 119:231–239.
as the middle and older age categories, young traits of Calce SE, Rogers TL. 2011. Evaluation of age estimation tech-
the acetabulum are more easily discernible due to the nique: Testing traits of the acetabulum. J Forensic Sci 56:
density, general smoothness, robusticity, and minimal 302–311.
porosity. Young adult females (n 5 4) are largely under- Cunha E, Baccino E, Martrille L, Ramsthaler F, Prieto J, Schu-
represented in the test sample (Table 8), which is attrib- liar Y, Lynnerup N, Cattaneo C. 2009. The problem of aging
uted to a general lack in available female specimens for human remains and living individuals: a review. Forensic Sci
Int 193:1–13.
study in modern late 20th century samples (Marks,
Fleiss JL, Cohen J. 1973. The equivalence of weighted kappa
1995; Grivas and Komar, 2008). That said, skeletal col- and the intraclass correlation coefficient as measures of reli-
lections with a large percentage of female specimens, ability. Educ Psychol Meas 33:613–619.
such as Hamann-Todd or Robert J. Terry would also be Franklin D. 2010. Forensic age estimation in human skeletal
appropriate. remains: current concepts and future directions. Legal Med
Applicability of this method to nonwhite populations 12:1–7.
must be explored. The investigator plans to test this Grivas CR, Komar DA. 2008. Kumho, Daubert, and the nature
method on available collections of various geographical of scientific inquiry: implications for forensic anthropology.
origins and encourages other researchers to do the same. J Forensic Sci 53:771–776.
Figures 1–6 may serve as datasheets in the estimation Haglund WD. 1997. Dogs and coyotes: postmortem involvement
with human remains. In: Haglund WD, Sorg MH, editors.
of age for an unknown individual. Morphological fea-
Forensic taphonomy: the postmortem fate of human remains.
tures of the acetabulum can be used as an effective age Boca Raton: CRC Press LLC. p 367–381.
indicator. The acetabulum is a durable part of skeleton, Hintze J. 2006. NCSS, PASS and GESS. NCSS. Kaysville, Utah.
which survives well in postdepositional environments Hoppa RD, Vaupel JW. 2002. The Rostock manifesto for paleode-
(Haglund, 1997), making the os coxae an important mography: the way from stage to age. In: Hoppa RD, Vaupel
region of study for methods of personal identification. In- JW, editors. Paleodemography: age distributions from skeletal
vestigator confidence using the author’s method is high, samples. Cambridge: Cambridge University Press. p 1–8.
but whenever possible should be combined with multiple _ can MY. 1989. Age markers in the human skeleton. Spring-
Is
age indicators for the most precise estimation of age-at- field, IL: Charles C. Thomas.
death. The present technique produces encouraging Komar DA, Lathrop S. 2006. Frequencies of morphological char-
acteristics in two contemporary forensic collections: implica-
results, can be completed on a small budget, and within
tions for identification. J Forensic Sci 51:974–978.
a reasonable amount of time. Consistency in scoring, Konigsberg LW, Herrmann NP, Wescott DJ, Kimmerle EH.
reduction in data collection time, and low error rates are 2008. Estimation and evidence in forensic anthropology: age-
significant advantages to using the technique, which is at-death. J Forensic Sci 53:541–557.
flexible and useful in forensic and bioarchaeological anal- Landis JR, Koch GG. 1977. The measurement of observer agree-
yses of human remains. ment for categorical data. Biometrics 33:159–174.
Lin LI-K. 1989. A concordance correlation coefficient to evaluate
ACKNOWLEDGMENTS reproducibility. Biometrics 45:255–268.
Lovejoy CO, Meindl RS, Pryzbeck TR, Mensforth RP. 1985.
The author thanks the following people: Drs. Helen K. Chronological metamorphosis of the auricular surface of the
Kurki, Tracy L. Rogers, and Michael Schillaci for critical ilium: a new method of determination of adult skeletal age at
review of the study proposal and/or editorial suggestions death. Am J Phys Anthropol 68:15–28.
of the manuscript; Joyce Hui, biomedical communications Lucy D, Aykroyd RD, Pollard AM, Solheim T. 1996. A Bayesian
approach to adult human age estimation from dental obser-
artist, for producing acetabular renderings; Drs. Heather
vations by Johanson’s age changes. J Forensic Sci 41:189–
J. Edgar and Lee Meadows Jantz for granting access to 194.
skeletal collections; graduate students Catherine Merritt, Manly BFJ. 2005. Multivariate statistical methods: a primer,
Lelia Watamaniuk, and Johanna Kelly for collaborating in 3rd ed. Boca Raton: Chapman and Hall.
testing observational consistency of the variables; and Dr. Marks J. 1995. Human biodiversity: genes, race, and history.
Christopher Ruff as well as three anonymous reviewers New York: Aldine de Gruyter.
for helpful comments on the manuscript. Meindl RS, Lovejoy CO, Mensforth RP, Walker RA. 1985. A re-
vised method of age determination using the os pubis, with a
review and tests of accuracy of other current methods of pubic
symphyseal aging. Am J Phys Anthropol 68:29–45.
LITERATURE CITED Meindl RS, Russell KF, Lovejoy CO. 1990. Reliability of age at
death in the Hamann–Todd collection: validity of subselection
Bartko JJ. 1976. On various intraclass correlation reliability procedures used in blind test of the summary age technique.
coefficients. Psychol Bull 83:762–765. Am J Phys Anthropol 83:349–357.
Bocquet-Appel JP, Masset C. 1982. Farewell to paleodemogra- Portney LG, Watkins MP. 2000. Foundations of clinical
phy. J Hum Evol 12:321–333. research: applications to practice, 2nd ed. Upper Saddle River,
Bedford ME, Russell KF, Lovejoy CO, Meindl RS, Simpson SW, NJ: Prentice-Hall.
Stuart-Macadam PL. 1993. Test of the multifactorial aging Rissech C, Estabrook GF, Cunha E, Malgosa A. 2006. Using the
method using skeletons with known ages-at-death from the acetabulum to estimate age-at-death of adult males. J Foren-
Grant Collection. Am J Phys Anthropol 91:287–297. sic Sci 51:213–229.
Boldsen JL, Milner GR, Konigsberg LW, Wood JW. 2002. Transi- Rissech C, Estabrook GF, Cunha E, Malgosa A. 2007. Estima-
tion analysis: a new method for estimating age from skele- tion of age-at-death for adult males using the acetabulum,