Anthropology · Vol. 5, No. 2 · 2022 · pp. 31–42 · e-ISSN 2473-4772

Assessing the Occipital Condyles for Age Estimation of Non-Adults

Gwyn D. Madden, Sango Otieno, Jordan Karsten

Department of Anthropology, Grand Valley State University, 1 Campus Drive, Allendale, MI 49401, USAUnited States
Department of Anthropology, Global Religions and Cultures, University of Wisconsin, Osh-Kosh 800 Algoma Blvd. Oshkosh,WI 54901, USAUnited States

DOI: https://doi.org/10.17140/antpoj-5-129 · Published 2022-05-25 · Licence: https://creativecommons.org/licenses/by/4.0 · © 2022 The Author(s)

Abstract

Objectives New methods for assessing age of non-adult remains are frequently sought to improve the ability to correctly identify individuals in for forensic and archaeological purposes. Especially when faced with comingled remains, it is helpful to have a bone appropriate tool for age estimation. Research was carried out to assess the usefulness of the occipital condyles for aging non-adult individuals using metric and morphology analyses. The research population included occipital condyles, both fused and unfused, of individuals of known age at death non-adult from the from the Hamann-Todd Collection, Museum of Natural History, Cleveland, Ohio, USA (N=69); Colecção Esqueletos Identificados, Natural History Museum, University of Coimbra, Portugal (N=113); Museu Bocage, National Museum of Natural History, Lisbon, Portugal (N=60). Length and width measurements were taken then regression was used to analyse the datasets. Three morphological factors were observed including, level of fusion at the synchondrosis intraoccipitalis anterior, presence/absence of billows and presence/absence of depressions. Results Accuracy based on the metric model ranged between 37-71%. The morphological model showed fusion present as early as 3-years of age, with all non-adults over 8-years showing 100% complete fusion. Only individuals below 13-years of age displayed billows or depressions present; presence not absence of the morphological variables can be used to estimate age with a 92% accuracy rate. Conclusion The metric model does not reach an acceptable level of accuracy for use in aging non-adults. Morphology of the occipital condyles do not follow a specific age progression but can be used as a quick age assessment guide; if these morphological features are present the individual very likely between 3-13-years of age.

Keywords: Age; Non-adult; Occipital condyle; Osteology; Skeletal; Juvenile; Aging; Forensic

Results

Accuracy based on the metric model ranged between 37-71%. The morphological model showed fusion present as early as 3-years of age, with all non-adults over 8-years showing 100% complete or depressions present; presence not absence of the morphological variables can be used to estimate age with a 92% accuracy rate.

Conclusion

The metric model does not reach an acceptable level of accuracy for use in aging non-adults. Morphology of the occipital condyles do not follow a specific age progression but can be used as a quick age assessment guide; if these morphological features are present the individual very likely between 3-13-years of age.

Keywords

Age; Non-adult; Occipital condyle; Osteology; Skeletal; Juvenile;

Introduction

he basilar portion of the occipital bone and the occipital condyles are osteological elements frequently encountered by T anthropologists in the field. Their relatively thick structures allow them to survive even in cases of poor preservation. Therefore, methods for identification of demographic variables employing this region of the skeleton would be particularly useful.

Research has been carried out on the occipital condyles 5-9 10 of adults in attempts to create sex and biological affinity based methods for use in analysis of unknown individuals. The condyles have also been used with three dimensional (3D) imaging in ascc Copyright 2022 by Madden GD. This is an open-access article distributed under Creative Commons Attribution 4.0 International License (CC BY 4.0), which fusion. Only individuals below 13-years of age displayed billows

Aging; Forensic.

sociation with the first cervical vertebra to aid in individuation in commingled situations.11

Research focusing on estimation of sex has been based 1-4 on the ranges of sizes between males and females in the occipital, 12-14 15,16 measured with hand held calipers and radiological images to calculate size and area; both of which are considered to be consistent data collection. Depending on geographic region the fo- 17 16,18 ramen magnum was included in some and excluded in other discriminant function analyses based on the “complete” crania to estimate sex. These models also require that geographic population is known prior to estimation of sex for an unidentified individual.

Few specifically included measurements of the occipital condyles 7,9,15 in their models.

Traditionally researchers estimate age for non-adult skeletal remains based on the eruption or calcification, of the dentition. In cases where teeth are absent, epiphyseal fusion and long bone lengths can be used to estimate age. Many archaeological and forensic contexts include fragmentary and comingled skeletal remains, precluding the application of these traditional methods. In situations where traditional methods cannot be employed, alternative methods are needed to assess age in non-adults. In fact, Rissech et al31 state some authors have recently highlighted the need to increase and diversify the number of growth models based on direct measurements from documented osteological material, to elaborate reference data concerning the development of each skeletal element and to deepen our understanding of the development of the different populations.

Research on the basicranium of non-adults has been studied as a potential way to estimate age for unknown individu- 3,32-34 als. It has been observed that just following birth the size of the pars lateralis increases significantly, with complete fusion of the four parts (pars lateralis, pars basilaris, squama) between 6-8-years of age, therefore by 6-8-years of age the area around the foramen magnum is close to the final adult size. A few of the studies have used archaeological samples observing the dentition or long bones to estimate age for comparison with occipital aging models. Many of these previously observed studies were individuals under 8-years of age and all were affected by small total sample sizes and for each year of life. As with studies conducted for sexing of adults, few of the studies of non-adults have included the occipital condyles specifically although there are a few exceptions. Standerwick et al observed that there is a measurable change with age in the length of the angle of the anterior aspect of the condyles but do not present a method for age estimation.

Redfield’s early research found metric change in the basicranium of non-adults that appeared stable across several samples, although sample sizes were small. Further, Redfield4 discussed the presence of morphological change occurring on the condyles calling them “condylar fossae”. The fossae do not occur where the condyles fuse together but at the canalis hypoglossi. He states that the “condylar fossae” appear with the beginning of fusion between the pars lateralis and pars basilaris, and that in most individuals over the age of 12 this area has become smooth. Although it was also noted that occasionally an adult might have a persistent fossae in this location. Furthermore, authors agree that genetic disorders4 or resource deprivation do not affect growth and develop- 37,38 ment of the basicranium. Use of the basicranium could be used in most cases where non-adults required aging.

Redfield’s4 research described the development of the occipital for specific age ranges to use in archaeological and forensic applications. However, it was developed using a skeletal sample where the age at death was unknown. The goal of the current study was to develop a system for aging similar to Redfield with specific focus on the occipital condyles.

Observations of the occipital condyles by the authors during previous research suggested that a process of morphological change was occurring during the course of development. The condyles of non-adults display billowing, depressions, grooves, 19-22 23-26 and an even surface, changes that are similar to those observed 39 40-42 on the bones of the auricular surface, pubic symphysis, and 28-30 43,44 sternal rib ends. A similar pattern is observed during growth and development of billowing in non-adults and flattening with advancing. Thus, it was hypothesized that a relationship existed between the morphological features observed on the occipital condyles and age.

Another goal of the present study was to establish definitions for occipital condyle measurements developed specifically for unfused non-adults and fused adult/non-adult skeletal elements.

31p. 202 Previous research suggests that both metric and morphological change can be used to estimate differences in age based on the basicranium. The current research expands upon these earlier studies.

Methods

The data collection procedure was two-fold, including both mor- 3,9 phological and metric analyses. Two types of measurements, length (left occipital condyle length (LOCL)/right occipital condyle 33,34 length (ROCL)) and width (left occipital condyle width (LOCW)/ right occipital condyle width (ROCW)), were used to estimate the relationship between the size of the occipital condyles and age. Measurement descriptions for length and width of fused and unfused occipital condyles are as follows: 13,14,35,36

Adult/Fused Condyles

Maximum length of the occipital condyle-anterior to posterior margins of articular surface of the occipital condyle in the sagittal plane (Figure 1).

Figure 1. Fused (left) and Partially Fused (right) Measurements of Occipital Condyle Length/Width (A=Length, B=Width) 31,p. 208 4 Maximum width of the occipital condyle-greatest width of the condyle perpendicular to length (Figure 1).

Non-adult/Unfused Condyles

Maximum length of the occipital condyle-anterior to posterior margins of articular surface of the occipital condyle portion of pars lateralis in the sagittal plane (Figure 2).

Figure 2. Unfused Non-Adult Measurements of Occipital Condyle Length/Width (A=Length, B=Width) Maximum width of the occipital condyle-greatest width of the condyle on pars lateralis perpendicular to length (Figure 2).

When taking the width measurements, if a natural groove transected the margin medially, the medial measurement was taken from the articular edge (groove is not included; Figure 3). All measurements were carried out with digital Mitutoyo calipers to the nearest 0.05 mm. Measurements were collected when possible on the left and right sides of the occipital condyles to test for variance. The ability to use either condyle alone may be needed in forensic and bioarchaeological cases.

Figure 3. Depression Breaking Margin (black arrows) and Bifurcated Condyle (circled in black) The morphological analysis sought to develop descriptive features of the condyles based on changes in shape. This was per- formed via gross visual observation of the condyles, described as follows, Billowing-low, rolling, medio-laterally positioned bumps

(Figure 4).

Depression-low relief circular, oval, and star shapes (Figure 4), enclosed on all sides; any depression crossing the medial margin does not fit this category and is a normal variation seen in

adults and non-adults;

Grooves-low relief linear depression (Figure 4), enclosed on all sides; any groove crossing the medial margin does not fit this category and is a normal variation seen in adults and non-adults. Also excluded are the anterior suture lines on unfused condyles.

Figure 4. Occipital Condyles Showing a (A) Depression, Groove (B), and Billow (C) Nomenclature shown above describing the occipital con- dyles was purposefully similar to that used in describing the auric- 39 40-42 ular surface and pubic symphysis to simplify the descriptive terms across methods of visual observation i.e. billowing.

These morphological features were recorded as present or absent and stage of fusion was observed as absent, partial, and completed.

Condyles from three skeletal collections with known demographic information were assessed in this study. The hamann-todd collection (HTC) housed at the Cleveland Museum of Natural History provided 69 non-adults who died between 1912 and 1938.45 The Colecção Esqueletos Identificados housed at the Laboratory of Forensic Anthropology of the Life Sciences Department at the University of Coimbra Portugal, was made up of individuals that died between 1915 and 1942,46 providing 113 non-adults for observation. The Museu Bocage (MB) in Lisbon (National Museum of Natural History) provided 60 non-adults 32,47 for observation, who died between 1880 and 1984. The skeletal remains from these three collections have thorough documentation making them excellent samples to use in the creation of the method outlined in this current research. Individuals ranging from fetal age to 18-years of age were observed. This resulted in a total of 242 individuals used in the morphological portion and 224 individuals formed the metric portion of the analysis as shown in Figure 5. Sex was recorded along with age, biological affinity and stage of fusion from the files accompanying the remains to assess variability for the HTC individuals only. While Redfield4 suggested pathological change in the basicranium did not affect growth and development individuals included in the current study were observed for presence or absence of pathology in the current study for consistency.

The canonical discriminant analysis (a dimension-reduction technique related to principal components and canonical correlation) procedure in SAS 9.4 was used to obtain a set of linear

combinations of the quantitative variables (ROCL, ROCW, LOCL and LOCW). These best reveal the differences among age (classification variable), sex (female/male), and stage of fusion (fused/ unfused).

Figure 5. Number of Individuals by Age Category and Sample The approximate F-test tests the hypothesis that the giv- en canonical correlation and all smaller ones are equal to zero in the population. The first tests if either dimension is significant and the second tests if dimension 2 by itself is significant. Larger val- ues for the F statistic show better correlation, and can have similar

significance to p-values of 0.0001.

Linear regression with backward selection was also car-

Table 1. General Descriptive Statistics for all Cities, HTC, EI and MB

Variable N Mean Minimum Median Quartile Maximum

All Cities

ROCL 230 21.49 4.34 20.18 ROCW 226 9.67 2 20.73 LOCL 225 21.41 4.37 20.41 LOCW 223 10.05 1.96 19.47

Htc

ROCL 68 19.24 5.52 28.72 ROCW 67 8.71 2.19 25.12 LOCL 65 19.09 5.61 29.37 LOCW 65 9.6 2.71 28.26

Ei

ROCL 102 23.17 2.34 10.08 ROCW 101 10.42 1.77 16.95 LOCL 103 22.92 2.88 12.56 LOCW 99 10.61 1.44 13.53

Mb

ROCL 60 21.19 4.26 20.11 ROCW 58 9.47 1.65 17.42 LOCL 57 21.34 3.87 18.15 LOCW 59 9.61 1.45 15.04 HTC: Hamann-todd collection; EI: Elimination; MB: Museu bocage; ROCL: Right occipital condyle length; ROCW: Right occipital condyle width; LOCL: Left occipital condyle length; LOCW: Left occipital condyle width.

ried out using SAS 9.4 to create age estimation formulae to be used by location and variable. The R2 produced by linear regression represents the percent of variance between the dependent variable and the independent variable. Values for R2 range from 0 to 1, with larger values suggesting increased linear correlation.

Intraobserver error measurements were taken on the HTC sample by the first author four weeks apart on a randomized sample of 12 individuals. The second author observed a randomized sample of 22 individuals from the HTC population four weeks following the first author’s original measurements to assess interobserver error. The absolute technical error of measurement (TEM) and relative technical error of measurement (rTEM) were calculated to test measurement precision for intra- and interob- 6,48 server error, as they are broadly applied for measuring precision.6,48 rTEM offers a percentage of error while TEM shows the error in the same units as the original measurements; TEM values can be used as a form of standard deviation between repeated measurements.49 The coefficient of reliability (R) was also calculated for intra- and interobserver error, with an output range between 0 and 1. Values closer to 1 show excellent reliability for each measure.48

Regarding morphology, intraobserver error was observed for the HTC sample by the first author on a randomized sample of 11 individuals, while the second author observed a randomized sample of 20 individuals from the same HTC sample. McNemar’s test was used to explain the error for intra- and interobserver error for morphology change.

Measurements

Standard Coefficient Lower Deviation of Variation Quartile

6.95 19.81 22.63 24.23 27.8 1.16 8.55 9.79 10.74 19.5 6.51 19.99 22.36 24.22 28.6 3.47 8.96 10.18 11.08 21.2

6.95 14.59 21.3 23.4 26.8 1.16 7.86 9.24 9.97 12.6 6.51 14.92 21.14 23.39 27.3 3.47 8.3 9.9 10.97 21.2

16.6 21.77 23.46 24.64 27.8 6.55 9.37 10.2 11.34 19.5 13 20.9 22.91 24.96 28.6 6.87 9.58 10.62 11.4 14.5

10.2 18.33 22.23 24.14 27.4 5.44 8.17 9.69 10.58 14.5 10.6 19.86 22.26 23.43 27.6 6.11 8.48 9.83 10.52 14.1

Results And Discussion

Metrics

No pathologies on the basicranium were identified during observation of the three samples. Table 1 displays descriptive statistics for the three collections separately and the three pooled together. Results of summary dimension reduction for canonical discriminant analyses illustrating a set of linear combinations of the quantitative variables (ROCL, ROCW, LOCL and LOCW) that best reveal the

Table 2. Canonical Discriminant Analyses for All Cities, HTC/MB, EI, MB, and HTC

City Variable Dimension for RV vs LV Dimension for RV vs LV and G Dimension for RV vs LV and E Dimension RV vs LV and F Right Variables 1 2 1 ROCL 0.17 -0.19 ROCW 0.05 0.53 HTC/El/MB Left Variables and Demographics LOCL 0.17 -0.26 LOCW 0.06 0.88 Right Variables ROCL 0.18 -0.21 ROCW 0.08 0.67 HTC/MB Left Variables and Demographics LOCL 0.18 -0.30 LOCW 0.09 0.86 Right Variables

ROCL 0.56 -0.34

ROCW 0.14 0.32 El Left Variables and Demographics LOCL 0.48 -0.21 LOCW 0.24 1.18 Right Variables ROCL 0.22 -0.17 ROCW 0.03 0.92 MB Left Variables and Demographics LOCL 0.22 -0.25 LOCW 0.09 1.10 Right Variables ROCL 0.17 -0.21 0.18 ROCW 0.08 0.61 0.07 Left Variables and Demographics HTC LOCL 0.16 -0.32 0.16 LOCW 0.10 0.82 0.09 Gender 0.09 Bio. Affin.

Fused

differences among age using each of the three samples as well as the combined data are summarized in Table 2. Additional variables are also noted in Table 2 for the HTC including sex (female/ male), biological affinity (black/white), and state of fusion (fused/ unfused). A summary data reduction dimensions and canonical correlation analysis are shown in Table 3.

The current research shows that dimensions 1 and 2 are each significant for side, sex, biological affinity, and fusion. Since the p-value is equal to <0.0001, less than the standard 0.05 indica-

2 1 2 1 2 -0.21 0.17 -0.21 0.18 -0.21 0.61 0.08 0.61 0.07 0.61

-0.14 0.16 -0.27 0.15 -0.08 0.54 0.10 0.44 0.09 0.60 -1.80 -0.06 1.97 0.27 -2.11

Table 3. Data Reduction Dimensions and Canonical Correlation Analysis

Canonical Coefficient City Dimension Canonical Correlation of Variation

Cleveland 1 0.95201 0.94855 0.017102 Bio. Affin.

Cleveland 2 0.29445 0.24827 0.166744 Bio. Affin.

Cleveland 1 0.95544 0.95223 0.015909 Fused Cleveland 2 0.33136 0.29257 0.162527 Fused Cleveland 1 0.95265 0.94919 0.016881 Sex Cleveland 2 0.41223 0.38580 0.151549 Sex Cleveland 1 0.95187 0.95006 0.017150 No Demographics Cleveland 2 0.23260 . 0.172697 No Demographics Cleveland- Coimbra- 1 0.97037 0.96981 0.007732 Lisbon Cleveland- Coimbra- 2 0.18497 . 0.127921 Lisbon Cleveland- 1 0.95961 0.95858 0.011931 Lisbon Cleveland- 2 0.31742 . 0.135566 Lisbon Coimbra 1 0.91649 0.90794 0.046200

Coimbra 2 0.19360 . 0.277856

Lisbon 1 0.98607 0.98494 0.007674

Lisbon 2 0.45587 . 0.219711

tor of significance it was concluded that the canonical correlations are not zero and therefore represent linear relationships within each of the variables.

The approximate F-test tests the hypothesis that the given canonical correlation and all smaller ones are equal to zero in the population. The first tests if either dimension is significant (F=145.95, 4, 408, <0.0001). The second tests if dimension 2 by itself is significant (F=29.55, 1, 205, <0.0001). Therefore, dimensions 1 and 2 are both significant. Since p≤0.0001 is less than 0.05 we can conclude that the canonical correlations are not zero and there is a linear relationship between the two groups of variables.

The squared canonical correlation for 1 and 2 combined is 0.806368. That is, approximately 80.6% of the variation in set 1 is explained by set 2, or vice versa. Hence, one could employ either set one (left) measurements or set two (right) measurements. It appears that age distribution drastically affects the squared canonical correlation for 1 and 2 combined. Note for Coimbra the squared canonical correlation is about 34%.

For HTC biological affinity, sex, and fusion the first ca-

Adjusted Approximate Squared F, Num df, Standard Canonical Eigenvalue Proportion Den df, Correlation Error Correlation p-value

20.96, 6, 52, 0.90633 9.6757 0.9903 27.8 <0.0001 1.28, 2, 27, 0.08670 0.0949 0.0097 19.5 0.2939 22.45, 6, 52, 0.91286 10.4762 0.9884 28.6 <0.0001 1.67, 2, 27, 0.10980 0.1233 0.0116 21.2 0.2080 22.62, 6, 52, 0.90754 9.8154 0.9796 26.8 <0.0001 2.76, 2, 27, 0.16994 0.2047 0.0204 12.6 0.0809 31.79, 4, 54, 0.90606 9.6457 0.9941 27.3 <0.0001 1.60, 1, 28, 0.05410 0.0572 0.0059 21.2 0.2161 86.71, 4, 108, 0.94163 16.1309 0.9978 27.8 <0.0001

1.95, 1, 55, 0.03421 0.0354 0.0022 19.5 0.1684 56.34, 4, 82, 0.92086 11.6356 0.9905 28.6 <0.0001 4.71, 1, 42, 0.10076 0.1120 0.0095 14.5 0.0358 6.97, 4, 18, 0.83996 5.2483 0.9926 27.6 0.0014 0.39, 1, 10, 0.03748 0.0389 0.0074 14.1 0.5466 28.77, 4, 20, 0.97233 35.1428 0.9926 14.1 <0.0001 2.89, 1, 11, 0.20782 0.2623 0.0074 14.1 0.1174

nonical correlation coefficients are above 0.95 with an explained variance of the correlation above 98%, eigenvalues of 10-11.2973, and p<0.0001.

A one unit increase in ROCL leads to a 0.21 unit increase in the first variate of the Right measurements (“Right1”), when ROCW is held constant and a one unit increase in LOCL leads to a 0.20 unit increase in the first variate of the Left measurements (“Left1”), when LOCW is held constant.

The first canonical correlation coefficient for HTC (without demographics) and Lisbon are over 0.91, with explained variance of correlation of 96-98%. All Cities almost reach 90% for the first canonical correlation coefficient at 0.897980 with an explained variance of the correlation of 96.65%, and a p<0.0001.

Coimbra provided a much different first canonical correlation coefficient of 0.582923, with an explained variance of the correlation of 77.47%, and a p<0.0001.

Using only Lisbon and Cleveland combined the R2 is 58%. Including Coimbra in the All Cities sample increases the

overall categorical size but decreases the R2 considerably.

The adjusted R2 for the linear combination of the measured variables (LOCW, LOCL, ROCW, ROCL) and age using backward elimination are 0.70, 0.33, and 0.43 for HTC, MB and All Cities combined respectively (Table 4). All variables were removed using backward elimination (EI) leaving the intercept only. The following are equations meant to produce estimated age using linear regression with backward selection:

All Cities: Predicting age using left and right measurements

Age=-10.05559+(0.42252*ROCL)+(0.33422*LO - CL)+(0.60259*LOCW)

Coimbra: Predicting age using left and right measurements

None with statistical significance to create an equation for prediction.

Lisbon: Predicting age using left and right measurements

Age=-8.57785+(0.98134*LOCL)

Cleveland: Predicting age using left and right measurements

Age=-12.57180+(0.87680*ROCL)+(0.49794*LOCW)

Cleveland: Predicting age using left and right measurements and

Table 4. Parameter Estimates and Fit Statistics Explaining AGE Linear Models

City Variable Estimate StdErr

Cleveland Intercept -11.81444 1.90241 (Bio. Affin.) Bio. Affin.=Black -2.62040 1.21898 n=64, Adj. R-Square=0.72, LOCL 0.84622 0.11064 RMSE=3.74 LOCW 0.71060 0.23903 Cleveland Intercept -8.15237 2.24440 (Fused) Fused=Yes 5.48057 1.72187 n=64, Adj. R-Square=0.74, LOCL 0.50296 0.15012 RMSE=3.59 LOCW 0.41729 0.22519 Cleveland Intercept -12.57180 1.91048 (No Demographics) n=65, ROCL 0.87680 0.11730 Adj. R-Square=0.70, RMSE=3.81 LOCW 0.49794 0.23671 Coimbra n=105, Adj. R-Square=0.00, RMSE=3.60 Lisbon Intercept -8.57785 4.10612 n=56, Adj. R-Square=0.33, RMSE=5.30 Cleveland/Coimbra/ Intercept -10.05559 1.81934 Lisbon ROCL 0.42252 0.15518 n=211, Adj. R-Square=0.43, LOCL 0.33422 0.14528 RMSE=4.43 LOCW 0.60259 0.18485

fused

Age=-8.15237+5.48057*Fused+0.50296*LOCL

Cleveland: Predicting age using left and right measurements and biological affinity

Age=-11.81444+-2.62040*Bio.Affinity+0.84622*LO- CL+0.71060*LOCW

TEM for intraobserver error suggested that the most reliable measurement was LOCW and the variable with the least reliability was LOCL. TEM for interobserver error showed ROCW as the most reliable measurement, while LOCL was the variable most affected by human error. Intraobserver rTEM ranged from 0.89 for ROCL to 2.36 for LOCL. Interobserver rTEM ranged from 1.07 for ROCL to 2.18 for LOCW. R2s were over 0.99 for each of the four measurements using TEM for intra- and inter-observer error. This suggests 99% of error is due to a factor other than author measurement error.

Box plots were prepared to observe if data lumping for all cities combined could be used as a strategy to create intervals for age estimation. Figure 6 illustrates the distribution of for each age group. The data indicate that size is not associated with a specific age (1-year of age) or specific age intervals (1-3-years of age). Instead the data suggest that the raw canonical coefficients should be interpreted in a manner analogous to interpreting regression coefficients i.e., for the variable age, a one unit increase leads to a

t Value Probt LowerCL UpperCL

-6.21 <.0001 -15.61983 -8.00905 -2.15 0.0356 -5.05872 -0.18208 7.65 <.0001 0.62491 1.06753 2.97 0.0042 0.23247 1.18874 -3.63 0.0006 -12.64184 -3.66291 3.18 0.0023 2.03632 8.92481 3.35 0.0014 0.20269 0.80324 1.85 0.0688 -0.03316 0.86774 -6.58 <.0001 -16.39079 -8.75282 7.48 <.0001 0.64232 1.11127 2.10 0.0395 0.02477 0.97112

Intercept 13.83810 0.35086 39.44 <.0001 13.14234 14.53385

-2.09 0.0414 -16.81013 -0.34557

LOCL 0.98134 0.18847 5.21 <.0001 0.60349 1.35919

-5.53 <.0001 -13.64240 -6.46879 2.72 0.0070 0.11659 0.72846 2.30 0.0224 0.04780 0.62063 3.26 0.0013 0.23816 0.96701

0.1449 increase in the first canonical variate when all of the other variables are held constant.

Figure 6. LOCL Box Plot for Samples Combined by Millimeters and Age

Morphology

The model was first applied to the HTC sample where four morphological factors were found to be associated with age, including stage of fusion, presence/absence of billowing, presence/absence of depressions, and presence/absence of grooves. Grooves that break the medial condylar margin and bifurcated condyles are not factors in aging (Figure 3). Fusion was present as early as 3-years of age and all non-adults over 8-years showed 100% complete fusion. If an individual’s condyles displayed fusion but still displayed grooves, billowing or depressions there was a 92% chance that they would fit into the 3-13-year-old age range. Generally flattened condyles were observed after age 13; however, 53% of unfused non-adults under three years of age were also flat. These results do not offer a “morphological method” but provide observations of morphological features present during the growth and development period from 3-13-years of age. Of the 196 fused individuals in the combined sample, 16 did not fit the pattern of fusion and were under aged.

For the HTC, 31 females and 37 males were observed.

One female and five males did not match the presence/absence expected for morphological features associated with age resulting in 10% of the population being aged incorrectly. Thirty-females and 30 males were observed for morphology from MB; of these there were one female and one male that did not present the morphological features associated with age. Thus, 6% of the individuals would have been misidentified in terms of age for the MB non-adults. At EI 55 females and 58 males were observed for morphology; eight males did not show the morphological features associated with age and thus these eight would have been assigned an incorrect age. Misidentification of age at EI was at 7%. Combined the three samples resulted in a total of 231 individuals, with 16 fused individuals misclassified, meaning 92% were given an accurate age using the presence/absence of the morphological features

defined here.

McNemar’s test, applied to study intraobserver error resulted in one disagreement for the variable of presence/absence of 11 individuals observed. McNemar’s test statistic suggests that there is not a statistically significant difference in the proportions of features described as presence/absence (p>1.000). Application of McNemar’s test to analyze interobserver error showed no discordant pairs between the two observers.

The EI sample population did not include individuals under the age of 6-years for observation making comparisons to the other sample populations unsuitable. The squamous cell carcinoma (SCC) values from the HTC show that if sex, biological affinity, or state of fusion are known specific equations would create more accurate age estimates (Table 4).

The following examples display application of equations from Table 4 to a 12-year-old female from the HTC collection.

HTC only

Age=-12.57180+(0.87680*ROCL)+(0.49794*LOCW)= 9.57 years+/-3.81 Age=-12.57180+(0.87680*24.62)+(0.49794*11.46)

All Cities Combined

Age=-10.05559+(0.42252*ROCL)+(0.33422*LO - CL)+(0.60259*LOCW)=15.41+/-4.43

Age=-10.05559+(0.42252*24.62)+(0.33422*24.46)+ (0.60259*11.46)

The HTC equation under aged this 12-year-old individual by ~2.5-years and for the All Cities combined equation the individual was over aged by ~3.5-years. If the root mean error is applied this individual would be within the ages of 5.7569 and 13.3831-years for the HTC only equation with a range of error 7.6262-years and between the ages of 10.98292 and 19.83708 using the All Cities model with a range of error 8.85416-years. Dental eruption by comparison ranges from +/-2-months to +/-36-months, total range of 6-years possible.27 Using the humerus as an example, standard deviations of long bone lengths can vary from between 5.42-12.11-years of age.50 Using the humerus again to look at fusion an age range between 17-24-years (head, distal epiphysis, and medial epicondyle)28 is suggested.

All three samples overlap by death dates and are considered to represent individuals of low to middle socio-economic sta- 31,51-53 tus. The fact that the method does not work in the Coimbra sample is likely due to the fact that there are no individuals under six years of age present. These ages in the developmental period normally show lack of fusion.

Although the two Portuguese samples are geographically close Inskip et al5 state that for sex “there is enough variation between the European groups…to significantly impact the accuracy of sex assessment 15p. 681 13 discriminant functions”. Veroni et al used length and width of the occipital condyles to assess sex in non-adults with a 75.8% accuracy for individuals over 8-years of age. On the other hand, Cardoso et al47 make the point that methods for age estimation should be both pooled and by sex; both were calculated for the HTC. In cases where sex is unknown the pooled population is best and when sex is known there would be an increase in the accuracy of the age estimate. In this paper it is suggested that methods for estimating non-adult age from occipital condyle measurements may still require populationally specific models as the three sample populations used here are mostly comprised of individuals of Western European descent. Socioeconomic status is considered low in all three collections but variation may also be present due to other environmental factors.5 These environmental factors and human growth in general can be quite variable mak- 31,54,55 ing some authors believe age estimation methods on samples such as these should be used with caution.

The majority of the remains in all three collections represent individuals that were deemed poorest of the poor and were not given the same burial treatment as those of higher socio-eco- 56 31 nomic status.56 Furthermore, Rissech et al31 discussed the size differences in children from Portuguese and English samples from the recent historic period with modern children and found that modern children are larger adding to an increase in temporal disparity. However, Redfield4 states that the base of the developing skull is stable and less likely to be affected even by conditions distorting the superior crania. This suggests the basicranium may not vary as other areas of the skeleton based on socioeconomic status and temporality. To better understand the effects of socio-economic status a study would need to research a sample of individuals with high socio-economic status.

TEM and R2 all show excellent precision between measurement trials for the first author and between authors indicating the measurements would be useful in future studies of non-adult occipital condyles. rTEM was only under 1% for intraobserver ROCL showing this to be the most reliable measurement. Together these show the measurements themselves are easily replicated.

Each morphological variant was distinct; presence of features were unable to be linked to “phases” or particular age ranges as seen in sternal rib ends, the auricular surface of the ilium, or pubic symphysis. While variation definitely exists in the developing occipital condyles, none of the specific changes, including billowing, depressions, and grooves, follow definable age ranges. Sixteen of the 196 fused individuals observed for morphological features did not fit into the age range 3-13, making the model 92% accurate. These observed changes do not include the medial depression that crosses the condyle’s margin or lines associated with complete or partial bifurcation of the condyles. This suggests that most of the morphological features seen on the occipital condyles are present between the ages of 3-13, encompassing the time the condyles begin and complete the fusion process. The upper age limit of 12

suggested by Redfield4 for disappearance of the “condylar fossae” fit within the method described here.

Conclusion

13p. 149-150 Measurements of length and width did not prove to be reliable methods for predicting age of the occipital condyles. As seen in prior studies total sample sizes of individuals under 6-years of age were small, only 26 at HTC and 15 at MB, where the metric method was significant. There were also no individuals represented for certain ages in this study including 2-years of age, 7 and 9-years of age for the HTC sample. To build upon the research presented here, additional data collection using documented collections focusing on increasing sample sizes, especially in certain age groups, are needed to improve our understanding of the potential for metric methods on the occipital condyles. As Standerwick et al35 observed change in the angle of the condyles during growth and development this is another area open to research potentially using 3D digitizer models.

Presence of billowing, depressions, and grooves can be used as a quick age assessment for the occipital condyles of unknown individuals to be between 3-13-years of age. Only presence, and not absence of billowing, depressions, or grooving can be used to estimate age. While morphological changes do exist on the condyles of non-adults the variation does not progress through specific morphological variables (ex. 1) billowing 2) billowing with depressions) at an identifiable pace. The changing morphology seen on the occipital condyles can age individuals between 3-13-years with 92% accuracy. The morphological changes of the occipital condyles allow researchers to meet the 80% accuracy Daubert criteria needed for forensic cases.57 Application of the morphological method should be limited to populations from similar geographic locations, the US and Southern Europe, those from the historic period to present, and those likely of lower socio-economic status. The morphological method should also be used in combination with other aging methods when possible. Even when considering the limitations, the morphological method adds a new tool to use in the age estimation of non-adult individuals in forensic cases, especially those with fragmented remains.

Instituitional Review Board Permission

Not needed.

Conflicts Of Interest

The authors declare that they have no conflicts of interest.

References

  1. TonevaDNikolovaSHarizanovS. Sex estimation by size and shape of the foramen magnum based on CT imaging. Leg Med (Tokyo). 2018; 35: 50-60. doi: 10.1016/j.legalmed.2018.09.00910.1016/j.legalmed.2018.09.009 https://doi.org/10.1016/j.legalmed.2018.09.009
  2. NagaokaTKawakuboYHirataK. Estimation of fetal age at death from the basilar part of the occipital bone. Int J Legal Med. 2012; 126: 703-711. doi: 10.1007/s00414-012-0718-210.1007/s00414-012-0718-2 https://doi.org/10.1007/s00414-012-0718-2
  3. Scheuer L, MacLaughlin-Black S. age estimation from the pars basilaris of the fetal and juvenile occipital bone. Int J Osteoarchaeol. 1991; 4: 377-380. doi: 10.1002/oa.1390040412 https://doi.org/10.1002/oa.1390040412
  4. RedfieldA. A new aid to aging immature skeletons: Development of the occipital bone. Am J Phys Anthropol. 1970; 33: 207- 220. doi: 10.1002/ajpa.133033020610.1002/ajpa.1330330206 https://doi.org/10.1002/ajpa.1330330206
  5. InskipSConstantinescuMBrinkmanAHooglandMSofaerJ. The effect of population variation on the accuracy of sex estimates derived from basal occipital discriminant functions. Achaeol Anthropol Sci. 2018; 10: 675-683. doi: 10.1007/s12520-016-0380-610.1007/s12520-016-0380-6 https://doi.org/10.1007/s12520-016-0380-6
  6. GapertRBlackSLastJ. Sex determination from the occipital condyle: discriminant function analysis in an eighteenth and nineteenth century british sample. Am J Phys Anthropol. 2009; 138: 384- 394. doi: 10.1002/ajpa.2094610.1002/ajpa.20946 https://doi.org/10.1002/ajpa.20946
  7. WestcottDJMoore-JansenPH. Metric variation in the human occipital bone: forensic anthropological applications. J Forensic Sci. 2001; 45: 1159-1163. doi: 10.1520/JFS15115J10.1520/jfs15115j https://doi.org/10.1520/jfs15115j
  8. WilliamsMM. Sex Determination of Fragmentary Crania by Analysis of the Cranial Base: Applications for the Study of an Arikara Skeletal Sample. [master’s thesis]. Knoxville, TN, USA: University of Tennessee; 1987
  9. HollandTD. Sex determination of fragmentary crania by analysis of the cranial base. Am J Phys Anthropol. 1986a; 70: 203-208. doi: 10.1002/ajpa.133070020710.1002/ajpa.1330700207 https://doi.org/10.1002/ajpa.1330700207
  10. HollandTD. Race determination of fragmentary crania by analysis of the cranial base. J Forensic Sci. 1986b; 31: 719-725. doi: 10.1520/JFS12305J10.1520/jfs12305j https://doi.org/10.1520/jfs12305j
  11. DudarJCCastilloER. Quantification of anatomical variation at the atlanto-occipital articulation: Morphometric resolution of commingled human remains within the repatriation documentation process. J Anat. 2016; 1-16. doi: 10.1111/joa.1256110.1111/joa.12561 https://doi.org/10.1111/joa.12561
  12. RamamoorthyBPaiMMPrabhuLVMuralimanjuBVRaiR. Assessment of craniometric traits in south indian dry skulls for sex determination. J Forensic Leg Med. 2016; 37: 8-14. doi: 10.1016/j. jflm.2015.10.00110.1016/j.jflm.2015.10.001 https://doi.org/10.1016/j.jflm.2015.10.001
  13. VeroniADejanaNSchillaciMA. Brief communication: Sexual dimorphism of the juvenile basicranium. Am J Phys Anthropol. 2010; 141: 147-151. doi: 10.1002/ajpa.2115610.1002/ajpa.21156 https://doi.org/10.1002/ajpa.21156
  14. GünayYAltmkökM. The value of the size of foramen magnum in sex determination. J Clin Forensic Med. 2000; 7: 147e9. doi: 10.1054/jcfm.2000.043010.1054/jcfm.2000.0430 https://doi.org/10.1054/jcfm.2000.0430
  15. Madadin M, Menezes RG, Al Saif HS, et al. Hamann-todd collection aging studies: Osteoporosis fracture syndrome. Am J Phys Anthropol. 1989; 80: 461-479. doi: 10.1002/ajpa.1330800406 https://doi.org/10.1002/ajpa.1330800406
  16. EkizogluOHocaogluEInciE. Assessment of sex in modern turkish population using cranial anthropometric parameters. Leg Med (Tokyo). 2016; 21: 45-52. doi: 10.1016/j.legalmed.2016.06.00110.1016/j.legalmed.2016.06.001 https://doi.org/10.1016/j.legalmed.2016.06.001
  17. KraniotiEFIşcanMYMichalodimitrakisM. Craniometric analysis of the modern cretan population. Forensic Sci Int. 2008; 180: 110.e1-110e5. doi: 10.1016/j.forsciint.2008.06.01810.1016/j.forsciint.2008.06.018 https://doi.org/10.1016/j.forsciint.2008.06.018
  18. SteynMIşcanMY. Sexual dimorphism in the crania and mandibles of south african whites. Forensic Sci Int. 1998; 98(1): 9-16. doi: 10.1016/s0379-0738(98)00120-010.1016/s0379-0738(98)00120-0 https://doi.org/10.1016/s0379-0738(98)00120-0
  19. AlQahtaniSJHectorMPLiversidgeHM. Accuracy of dental estimation charts: Schour and Massler, Ubelaker, and the London atlas. Am J Phys Anthropol. 2014; 154: 70-78. doi: 10.1002/ ajpa.22473
  20. HillsonS. Dental Anthropology. Cambridge, England: Cambridge Press; 1996
  21. UbelakerDH. Human Skeletal Remains: Excavation, Analysis, Interpretation (Aldine Manuals on Archeology). Oxford, England: Aldine Publishing Company; 1978
  22. SchourLMasslerM. The development of the human dentition. J Am Dent Assoc. 1941; 28: 1153-1160
  23. KamnikarKRHerrmanNPPlemonsAM. New approaches to juvenile age estimation in forensics: Application of transition analysis via the shackelford et al. method to a diverse modern subadult sample. Hum Biol. 2018; 90(1): 1-20. doi: 10.13110/humanbiology.90.1.0610.13110/humanbiology.90.1.06 https://doi.org/10.13110/humanbiology.90.1.06
  24. LiversidgeHM. Controversies in age estimation from developing teeth. Ann Hum Biol. 2015; 42(4): 395-404. doi: 10.3109/03014460.2015.104446810.3109/03014460.2015.1044468 https://doi.org/10.3109/03014460.2015.1044468
  25. DemirjianAGoldsteinHTannerJ. A new system of dental age assessment. Hum Biol. 1973; 45(2): 211-217
  26. MoorreesCFanningEHuntE. Age variation of formation stages for ten permanent teeth. J Dent Res. 1963; 42(6): 1490-1502. doi: 10.1177/0022034563042006270110.1177/00220345630420062701 https://doi.org/10.1177/00220345630420062701
  27. UbelakerD. Human Skeletal Remains: Excavation, Analysis, Inrd terpretation. 3 ed. Washington D.C, USA: Transaction Publishers; 1999
  28. BassW. Human Osteology: A Laboratory and Field Manual. (Special th Publication No. 2 of the Missouri Archaeological Society). 5 ed. Springfield, MO, USA: Missouri Archaeological Society; 2005
  29. BuikstraJEUbelakerDH. Standards for data collection from human skeletal remains. Paper presented at: The Field Museum of Natural History. Arkansas Archaeological Survey; 1994; Fayetteville, AR, USA
  30. FazekasIGKósaF. Forensic Fetal Osteology. Kiado, Budapest, Hungary: Akadémiai Kiadó; 1978
  31. RissechCLópez-CostasOTurbónD. Humeral development from neonatal period to skeletal maturity–application in age and sex assessment. Int J Legal Med. 2013; 127: 201-212. doi: 10.1007/ s00414-012-0713-7
  32. CardosoHFVGomesJCampanachoVMarinhoL. Age estimation of immature human skeletal remains using the post-nasal development of the occipital bone. Int J Legal Med. 2013; 127: 997- 1004. doi: 10.1007/s00414-013-0818-710.1007/s00414-013-0818-7 https://doi.org/10.1007/s00414-013-0818-7
  33. Alfonso-DurrutyMPThompsonJT. Basiocciput age at death estimation assessment in subadults from punta teatinos, chile. Anthropologie. 2011; XLIX(2): 125-132
  34. TocheriMWMoltoJE. Aging fetal juvenile skeletons from roman period egypt using basiocciput osteometrics. Int J Osteoarchaeol. 2002; 12: 356-363. doi: 10.1002/oa.63410.1002/oa.634 https://doi.org/10.1002/oa.634
  35. Standerwick RG, Roberts EW, Hartsfield Jr JK, Babler WJ, Katona TR. Comparison of the bolton standards to longitudinal cephalograms superimposed on the occipital condyle (I-point). J Orthod. 2009; 36: 23-35. doi: 10.1179/14653120722896 https://doi.org/10.1179/14653120722896
  36. UysalSGokharmanDKacarMTuncbilekIKosarU. Estimation of sex by 3D CT measurements of the foramen magnum. J Forensic Sci. 2005; 50: 1310-1314. doi: 10.1520/JFS200505810.1520/jfs2005058 https://doi.org/10.1520/jfs2005058
  37. CameronNDemerathE. Critical periods of growth and their relation to diseases of aging. Am J Phys Anthropol. 2002; 45: 159- 184. doi: 10.1002/ajpa.1018310.1002/ajpa.10183 https://doi.org/10.1002/ajpa.10183
  38. EllisonP. Evolutionary perspective on the fetal origins hypothesis. Am J Human Biol. 2005; 17(1): 113-118. doi: 10.1002/ ajhb.20097
  39. LovejoyCOMeindlRSPryzbeckTRMensforthRP. Chronological metamorphosis of the auricular surface of the ilium: A new method for the determination of age at death. Am J Phys Anthropol. 1985; 68: 15-28. doi: 10.1002/ajpa.133068010310.1002/ajpa.1330680103 https://doi.org/10.1002/ajpa.1330680103
  40. ToddTW. Age changes in the pubic bone. I. The male white pubis. Am J Phys Anthropol. 1921a; 3: 285-334. doi: 10.1002/ ajpa.1330030301
  41. ToddTW. Age Changes in the Pubic Bone. II: The Pubis of the Male Negro-White Hybrid, III: The Pubis of the White Female. IV: The Pubis of the Female Negro-White Hybrid. Am J Phys Anthropol. 1921b; 4: 517-549. doi: 10.1002/ajpa.133004010210.1002/ajpa.1330040102 https://doi.org/10.1002/ajpa.1330040102
  42. BrooksSSucheyJM. Skeletal age determination based on the os pubis: A comparison of the acsadi-nemeskeri and suchey-brooks methods. Hum Evol. 1990; 5: 227-238. doi: 10.1007/ BF02437238
  43. IşcanMYLothSR. Determination of age from the sternal rib in white males: A test of the phase method. J Forensic Sci. 1986a; 31: 122-132. doi: 10.1520/JFS11866J10.1520/jfs11866j https://doi.org/10.1520/jfs11866j
  44. IşcanMYLothSR. Determination of age from the sternal rib in white females: A test of the phase method. J Forensic Sci. 1986b; 31: 990-999
  45. Cleveland Museum of Natural History. Collections and Databases. http://www.cmnh.org/. Accessed February 1, 2022
  46. RochaMA. Les collections ostéologiques humaines identifiées du musée anthropologique de l’université de Comimbra. Anthropologia Portuguesa. 1995; 13: 7-38
  47. CardosoHFVAbrantesJHumphreyLT. Age estimation of immature human skeletal remains from the diaphyseal length of long bones in the postnatal period. Int J Legal Med. 2014; 128: 809- 824. doi: 10.1007/s00414-013-0925-510.1007/s00414-013-0925-5 https://doi.org/10.1007/s00414-013-0925-5
  48. JamaiyahHGeetaASafizaMN. Reliability, technical error of measurements and validity of length and weight measurements for children under two years old in Malaysia. Med J Malaysia. 2010; 65( Suppl A): 131-137
  49. StomfaiSAhrensWBammannK. Intra- and inter-observer reliability in anthropometric measurements in children. Int J Obes (Lond). 2011; 35: S45–S51. doi: 10.1038/ijo.2011.3410.1038/ijo.2011.34 https://doi.org/10.1038/ijo.2011.34
  50. JohnstonFE. Growth of the long bones of infants and young children at Indian Knoll. Am J Phys Anthropol. 1962; 20(3): 249-254. doi: 10.1002/ajpa.133020030910.1002/ajpa.1330200309 https://doi.org/10.1002/ajpa.1330200309
  51. CoqueugniotHWeaverTD. Brief communication: Infracranial maturation in the skeletal collection from coimbra, portugal: New aging standards for epiphyseal union. Am J Phys Anthropol. 2007; 134: 424-437. doi: 10.1002/ajpa.2068310.1002/ajpa.20683 https://doi.org/10.1002/ajpa.20683
  52. CardosoHFV. Brief communication: The collection of identified human skeletons housed at the Bocage Museum (National Museum of Natural History), Lisbon, Portugal. Am J Phys Anthropol. 2006; 129: 173-176. doi: 10.1002/ajpa.2022810.1002/ajpa.20228 https://doi.org/10.1002/ajpa.20228
  53. MensforthRPLatimerBM. Hamann-todd collection aging studies: Osteoporosis fracture syndrome. Am J Phys Anthropol. 1989; 80(4): 461-479. doi: 10.1002/ajpa.1330800406 de la Cova C. Patterns of trauma and violence in 19th-century-born African American and Euro-American females. Int J Paleopathol. 2012; 2(2-3): 61-68. doi: 10.1016/j.ijpp.2012.09.00910.1002/ajpa.1330800406 https://doi.org/10.1002/ajpa.1330800406
  54. LamplMJohnstonFE. Problems in the aging of skeletal juveniles: Perspectives from maturation assessments of living children. Am J Phys Anthropol. 1996; 101: 345-355. doi: 10.1002/(SICI)1096- 8644(199611)101:3<345:AID-AJPA4>3.0.CO;2-Y th10.1002/(sici)1096-8644(199611)101:3 https://doi.org/10.1002/(sici)1096-8644(199611)101:3
  55. Muller JL, Pearlstein KE, de la Cova C. Dissection and documented skeletal collections: Embodiments of legalized inequality. In: Nystrom KC, ed. The Bioarchaeology of Dissection and Autopsy in the United States, Bioarchaeology and Social Theory. New York, USA: Springer; 2017: 185-201
  56. Daubert v. Merrel dow pharmaceuticals, Inc., 509 U.S. 579. 1993. https://supreme.justia.com/cases/federal/us/509/579/. Accessed, 2022