Measuring the Tibia: Trotter's Error Revisited.

In Trotter and Gleser's (Am J Phys Anthropol 1952;10:463) classic study of stature estimation, a definition of the tibia length measurement is given that agrees with the standard condylar-malleolar length. That Trotter did not in fact measure according to her definition, but rather omitted the malleolus, has been well documented by Jantz et al. (J Forensic Sci 1995;40:758). Both the Terry collection and the World War 2 (WW2) samples were affected, although questions remain about the latter that cannot be resolved directly because it is no longer available for examination. Trotter's data from hundreds of servicemen are especially important because the statures were measured by technicians, rather than based on cadaver lengths or forensic statures. The questions examined in this note are as follows: Was WW2 measured uniformly in the same way as Terry; are there differences between Terry and WW2 that could influence estimation of the adjustment; and is the 10 millimeter (mm) adjustment proposed by Jantz et al. (J Forensic Sci 1995;40:758) still appropriate. Our analysis relies on a measurement taken by Trotter that is clearly and uniquely defined, what she called "ordinary length". This measurement was used to create expectations about how Trotter measured what she called maximum length of the tibia. Results provide no evidence that WW2 was measured any differently than Terry, with the exception of one small series. They also show slight morphological differences on the distal and/or proximal end of the tibia between Terry and WW2. Despite the slight difference, the adjustment to account for the malleolus is still valid.

Error quantification of osteometric data in forensic anthropology.

This study evaluates the reliability of osteometric data commonly used in forensic case analyses, with specific reference to the measurements in Data Collection Procedures 2.0 (DCP 2.0). Four observers took a set of 99 measurements four times on a sample of 50 skeletons (each measurement was taken 200 times by each observer). Two-way mixed ANOVAs and repeated measures ANOVAs with pairwise comparisons were used to examine interobserver (between-subjects) and intraobserver (within-subjects) variability. Relative technical error of measurement (TEM) was calculated for measurements with significant ANOVA results to examine the error among a single observer repeating a measurement multiple times (e.g. repeatability or intraobserver error), as well as the variability between multiple observers (interobserver error). Two general trends emerged from these analyses: (1) maximum lengths and breadths have the lowest error across the board (TEM<0.5), and (2) maximum and minimum diameters at midshaft are more reliable than their positionally-dependent counterparts (i.e. sagittal, vertical, transverse, dorso-volar). Therefore, maxima and minima are specified for all midshaft measurements in DCP 2.0. Twenty-two measurements were flagged for excessive variability (either interobserver, intraobserver, or both); 15 of these measurements were part of the standard set of measurements in Data Collection Procedures for Forensic Skeletal Material, 3rd edition. Each measurement was examined carefully to determine the likely source of the error (e.g. data input, instrumentation, observer's method, or measurement definition). For several measurements (e.g. anterior sacral breadth, distal epiphyseal breadth of the tibia) only one observer differed significantly from the remaining observers, indicating a likely problem with the measurement definition as interpreted by that observer; these definitions were clarified in DCP 2.0 to eliminate this confusion. Other measurements were taken from landmarks that are difficult to locate consistently (e.g. pubis length, ischium length); these measurements were omitted from DCP 2.0. This manual is available for free download online (https://fac.utk.edu/wp-content/uploads/2016/03/DCP20_webversion.pdf), along with an accompanying instructional video (https://www.youtube.com/watch?v=BtkLFl3vim4).

Differential Decomposition Among Pig, Rabbit, and Human Remains.

While nonhuman animal remains are often utilized in forensic research to develop methods to estimate the postmortem interval, systematic studies that directly validate animals as proxies for human decomposition are lacking. The current project compared decomposition rates among pigs, rabbits, and humans at the University of Tennessee's Anthropology Research Facility across three seasonal trials that spanned nearly 2 years. The Total Body Score (TBS) method was applied to quantify decomposition changes and calculate the postmortem interval (PMI) in accumulated degree days (ADD). Decomposition trajectories were analyzed by comparing the estimated and actual ADD for each seasonal trial and by fuzzy cluster analysis. The cluster analysis demonstrated that the rabbits formed one group while pigs and humans, although more similar to each other than either to rabbits, still showed important differences in decomposition patterns. The decomposition trends show that neither nonhuman model captured the pattern, rate, and variability of human decomposition.

The application of amplicon length heterogeneity PCR (LH-PCR) for monitoring the dynamics of soil microbial communities associated with cadaver decomposition.

The placement of cadavers in shallow, clandestine graves may alter the microbial and geochemical composition of the underlying and adjacent soils. Using amplicon length heterogeneity-PCR (LH-PCR) the microbial community changes in these soils can be assessed. In this investigation, nine different grave sites were examined over a period of 16weeks. The results indicated that measurable changes occurred in the soil bacterial community during the decomposition process. In this study, amplicons corresponding to anaerobic bacteria, not indigenous to the soil, were shown to produce differences between grave sites and control soils. Among the bacteria linked to these amplicons are those that are most often part of the commensal flora of the intestines, mouth and skin. In addition, over the 16week sampling interval, the level of indicator organisms (i.e., nitrogen fixing bacteria) dropped as the body decomposed and after four weeks of environmental exposure they began to increase again; thus differences in the abundance of nitrogen fixing bacteria were also found to contribute to the variation between controls and grave soils. These results were verified using primers that specifically targeted the nifH gene coding for nitrogenase reductase. LH-PCR provides a fast, robust and reproducible method to measure microbial changes in soil and could be used to determine potential cadaveric contact in a given area. The results obtained with this method could ultimately provide leads to investigators in criminal or missing person scenarios and allow for further analysis using human specific DNA assays to establish the identity of the buried body.

Secular change in craniofacial morphology.

Five craniofacial variables (glabella-occipital length, basion-bregma height, maximum cranial breadth, nasion-prosthion height, and bizygomatic breadth) were used to examine secular change in morphology from the mid-19(th) century to the 1970s. The 19(th) century data were obtained from the Terry and Hamann-Todd anatomical collections, and the 20(th) century data were obtained from the forensic anthropology databank. Data were available for Blacks and Whites of both sexes. Secular change was evaluated by regressing cranial variables on year of birth. Two analyses were conducted, one using the original variables and one using size and shape. Size is defined as the geometric mean of the cranial variables, and shape is the ratio of each variable to size. The results show remarkable changes in the size and shape of the cranial vault. Vault height increases in all groups in both absolute and relative terms. The vault also becomes longer and narrower, but these changes are less pronounced. Face changes are less than the vault changes, but to the extent that they occur, the face becomes narrower and higher. Overall cranial vault size has increased, but shape changes are greater than size changes. The magnitude of secular change in vault height exceeds that for long bones over a comparable time period, but follows a similar course, which suggests that vault height and bone length respond to the same forces. Changes in vault dimensions must occur by early childhood because of the early development of the vault. Am. J. Hum. Biol. 12:327-338, 2000. Copyright 2000 Wiley-Liss, Inc.