Archäologische und naturwissenschaftliche Untersuchungen zu spätantiken Gräbern in und bei den römischen Thermen von Grumentum

Die römische Stadt Grumentum liegt in Süditalien, im Innern von Lucanien, der heutigen Region Basilicata, etwa gleich weit vom ionischen und tyrrhenischen Meer entfernt, inmitten einer wunderschönen Landschaft, die zum einen durch das Agri-Tal und zum anderen durch hohe Berge gekennzeichnet ist. Diese Stadt war in der Antike ein bedeutendes Zentrum des Binnenlandes, da sie an einem wichtigen Straßenknotenpunkt lag. Von seinem wechselhaften Schicksal in der Geschichte berichten zahlreiche Schriftsteller, wie Livius von den punischen Kriegen – Hannibal stand auch hier vor den Toren – oder Appian von den Bürgerkriegen zu Beginn des ersten vorchristlichen Jahrhunderts. Außerhalb des Stadtgebietes sind vier monumentale Grabbauten, zahlreiche Grabinschriften und ein Aquaedukt gefunden worden. Von der Stadtbefestigung sind die Reste der Mauern unter üppigem Bewuchs noch verborgen. In der Stadt wurden bis jetzt das Forum, mehrere Tempel, ein Theater, ein Amphitheater und ein Wohnkomplex freigelegt. Zwischen 1999 und 2003 fanden erneut Ausgrabungen statt. Ein internationales Team unter der Leitung von Hansjörg Thaler konnte Teile der Straßen, einen weiteren Wohnkomplex und eine Thermenanlage – zunächst durch Prospektionen, dann in mehreren Grabungskampagnen – untersuchen. ..

Is amino acid racemization a useful tool for screening for ancient DNA in bone?

Many rare and valuable ancient specimens now carry the scars of ancient DNA research, as questions of population genetics and phylogeography require larger sample sets. This fuels the demand for reliable techniques to screen for DNA preservation prior to destructive sampling. Only one such technique has been widely adopted: the extent of aspartic acid racemization (AAR). The kinetics of AAR are believed to be similar to the rate of DNA depurination and therefore a good measure of the likelihood of DNA survival. Moreover, AAR analysis is only minimally destructive. We report the first comprehensive test of AAR using 91 bone and teeth samples from temperate and high-latitude sites that were analysed for DNA. While the AAR range of all specimens was low (0.02 -0.17), no correlation was found between the extent of AAR and DNA amplification success. Additional heating experiments and surveys of the literature indicated that D/L Asx is low in bones until almost all the collagen is lost. This is because aspartic acid is retained in the bone within the constrained environment of the collagen triple helix, where it cannot racemize for steric reasons. Only if the helix denatures to soluble gelatin can Asx racemize readily, but this soluble gelatine is readily lost in most burial environments. We conclude that Asx D/L is not a useful screening technique for ancient DNA from bone

Bias and accuracy of age estimation using developing teeth in 946 children

Developing teeth are used to assess maturity and estimate age in several disciplines. The aim of the study was to determine which of the most well known dental age estimation methods was best at estimating age. The target sample of dental radiographs ( N = 946, ages 3–16) was described by Maber et al. (Forensic Sci Int 159 ( 2006 ) S68–S73). Seven mandibular permanent teeth (I 1 –M 2 ) were assessed, and dental age was calculated using four dental maturity scales and fifteen methods that use data for individual teeth. The mean difference between dental age and real age was calculated (bias) as well as several other measures of accuracy (mean/median absolute difference, percentage aged to within six months and to within 10% of real age). Most methods estimated age with significant bias and standard deviation of bias ranged from 0.86 to 1.03 years. Analysis by age group showed most methods over-aged younger children, and considerably under-aged older children. The method that performed best was the dental maturity scale of Willems et al. (J Forensic Sci 46 ( 2001 ) 893–895) with bias of −0.14 ± 0.86 years ( N = 827), mean absolute difference of 0.66 years, 71% aged to 10% or less of age, and 49% aged to within six months. Two individual teeth, P 2 and M 2 , estimated age with bias not significantly different to zero for most formation stages using methods based on a large reference sample (L9a Demirjian stages) and a uniform age distribution (N25a Moorrees stages). Standard deviation of bias was least for early crown stages and most for late root stages. Methods that average ages for individual teeth improve if schedules for ‘mean age entering a stage’ are adjusted for prediction. Methods that directly calculate ‘mean age within stage’ can be improved by drawing from a uniform age distribution. Am J Phys Anthropol, 2010. © 2010 Wiley-Liss, Inc.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/78321/1/21349_ftp.pd

Evaluation of Lamendin’s age-at-death estimation method in a documented osteological collection (La Plata, Argentina)

Age estimation is one of the main biological parameters to be determined for constructing an individual biologicalprofile. In contexts where bones are poorly preserved, the use of teeth becomes relevant. Translucency of dentine has become relevant in recent decades, since the publication of the method proposed by Lamendin et al. (1992). In the local context, studies validating age-estimation methods from the permanent dentition are lacking. For this reason, it was decided to evaluate the performance of the age-estimation method proposed by Lamendin et al. (1992) in a sample of adult individuals with documented age belonging to the Lambre collection from the Municipal Cemetery of the city of La Plata. It was found that estimated age according to Lamendin et al.?s (1992) method varies by tooth type and age, being age the one that influences the estimates the most. On the other hand, sex has no influence in the estimation of age. The results showed no differences in the estimation in individuals between 35?50 years old, whileexhibiting a tendency to overestimate age in young adults and to underestimate it in older ones.Fil: Garizoain, Gonzalo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Petrone, Selene. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Plischuk, Marcos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Inda, Ana María. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas; ArgentinaFil: García, Marcela Nilda. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentin

A genome-wide association scan implicates <i>DCHS2, RUNX2, GLI3, PAX1</i> and <i>EDAR</i> in human facial variation

We report a genome-wide association scan for facial features in ∼6,000 Latin Americans. We evaluated 14 traits on an ordinal scale and found significant association (P values−8) at single-nucleotide polymorphisms (SNPs) in four genomic regions for three nose-related traits: columella inclination (4q31), nose bridge breadth (6p21) and nose wing breadth (7p13 and 20p11). In a subsample of ∼3,000 individuals we obtained quantitative traits related to 9 of the ordinal phenotypes and, also, a measure of nasion position. Quantitative analyses confirmed the ordinal-based associations, identified SNPs in 2q12 associated to chin protrusion, and replicated the reported association of nasion position with SNPs in PAX3. Strongest association in 2q12, 4q31, 6p21 and 7p13 was observed for SNPs in the EDAR, DCHS2, RUNX2 and GLI3 genes, respectively. Associated SNPs in 20p11 extend to PAX1. Consistent with the effect of EDAR on chin protrusion, we documented alterations of mandible length in mice with modified Edar function

The persistence of epiphyseal scars in the distal radius in adult individuals

The use of radiographic imaging in the estimation of chronological age facilitates the analysis of structures not visible on gross morphological inspection. Following the completion of epiphyseal fusion, a thin radio-opaque band, the epiphyseal scar, may be observed at the locus of the former growth plate. The obliteration of this feature has previously been interpreted as the final stage of skeletal maturation and consequently has been included as a criterion in several methods of age estimation, particularly from the distal radius. Due to the recommendations relating to age estimation in living individuals, accurate assessment of age from the distal radius is of great importance in human identification; however, the validity of the interpretation of the obliteration of the epiphyseal scar as an age-related process has not been tested. A study was undertaken to assess the persistence of epiphyseal scars in adults between 20 and 50 years of age through the assessment of 616 radiographs of left and right distal radii from a cross-sectional population. This study found that 86 % of females and 78 % of males retained some remnant of the epiphyseal scar in the distal radius. The relationships between chronological age, biological sex and the persistence of the epiphyseal scar were not statistically significant. The findings of this study indicate that the epiphyseal scars may persist in adult individuals until at least 50 years of age. No maximum age should therefore be applied to the persistence of an epiphyseal scar in the distal radius