Robustezza Strutturale e Marcatori di Stress Muscoloscheletrico a confronto in un campione dell'Eta del Bronzo

Parte della ricerca antropologica, negli ultimi trent'anni, si è impegnata in indagini volte alla ricostruzione dello stile di vita e delle abitudini delle popolazioni del passato e questo settore è in continua espansione. Gran parte delle pubblicazioni affronta l'argomento attraverso gli indicatori scheletrici di stress muscoloscheletrico (MSM) che si riferiscono alle zone dove muscoli e tendini si attaccano sull'osso. Gli MSM hanno ricevuto molte critiche da studi recenti (Stirland 1998; Weiss 2003, 2007; Zumwalt 2006) e la loro validità come indicatori di robustezza è stata messa in discussione. Questa ricerca vuole tentare di definire i rapporti tra MSM e robustezza strutturale delle ossa e valutare così l'utilità o meno degli MSM nella ricostruzione dei pattern di attività. Per fare ciò sono stati studiati gli omeri e i radii di 17 uomini (sepolti con armi) e 15 donne della necropoli dell'Età del Bronzo “l'Olmo di Nogara”. Su questo materiale è stato effettuato uno studio della geometria delle sezioni i cui risultati sono stati confrontati con i dati sugli MSM ottenuti attraverso due metodi diversi (uno quantitativo e uno qualitativo). Il primo di questi metodi è risultato inconclusivo, mentre il secondo ha mantenuto la sua validità. Inoltre, tentando di ricostruire le possibili attività degli individui esaminati (riguardanti per i maschi, in modo specifico, il tipo di armamento usato), è risultata molto utile l'applicazione della geometria delle sezioni congiuntamente agli MSM. In conclusione, lo studio ha confermato l'esistenza di una correlazione significativa fra stress muscolare e robustezza diafisaria e ha mostrato che l'integrazione tra i due metodi permette di ottenere informazioni non raggiungibili altrimenti

Environmental influence on the phenotype: Morphological variation in human dentition

This work is about the role that environment plays in the production of evolutionary significant variations. It starts with an historical introduction about the concept of variation and the role of environment in its production. Then, I show how a lack of attention to these topics may lead to serious mistakes in data interpretation. A statistical re-analysis of published data on the effects of malnutrition on dental eruption, shows that what has been interpreted as an increase in the mean value, is actually linked to increase of variability. In Chapter 3 I present the topic of development as a link between variability and environmental influence, giving a review of the possible mechanisms by which development influences evolutionary dynamics. Chapter 4 is the core chapter of the thesis; I investigated the role of environment in the development of dental morphology. I used dental hypoplasia as a marker of stress, characterizing two groups. Comparing the morphology of upper molars in the two groups, three major results came out: (i) there is a significant effect of environmental stressors on the overall morphology of upper molars; (ii) the developmental response increases morphological variability of the stressed population; (iii) increase of variability is directional: stressed individuals have increased cusps dimensions and number. I also hypothesized the molecular mechanisms that could be responsible of the observed effects. In Chapter 5, I present future perspectives for developing this research. The direction of dental development response is the same direction of the trend in mammalian dental evolution. Since malnutrition triggers the developmental response, and this particular kind of stressor must have been very common in our class evolutionary history, I propose the possibility that environmental stress actively influenced mammals evolution. Moreover, I discuss the possibility of reconsidering the role of natural selection in the evolution of dental morphology

At the upper Palaeolithic – Mesolithic boundary : revision of the human remains from Riparo Fredian (Molazzana, Lucca, Italy)

Abstract: Pleistocene and early Holocene human fossils in Tuscany are very few and poorly described. Any new information is thus an important contribution to our knowledge of the peopling of this region. Here we present a revision of the human fossil remains from the Riparo Fredian, a site located in Garfagnana and first published by Boschian et al., (1995). The authors described the human remains of the site pointing out the presence of 39 isolated human teeth (19 maxillary and 20 mandibular) and “fragments of one adult humerus, of a child's femur and of a youngster’s ulna”, considered as belonging to six individuals at least. A reanalysis of the human remains indicated that several specimens were incorrectly identified. It was thus deemed important to revise the identification of each fossil and their interpretation. The revision of human remains from Riparo Fredian has led to several changes in their anatomical identification with respect to the original publications. Of the 39 teeth previously described, the analysis revealed that two of them belonged to non-human animals, and 18 were mistakenly identified. A new, correct identification is provided for each of them. Also, two human teeth not described in the original papers have been identified. The anatomical identification of the post-cranial remains has been confirmed for two out of the three specimens. The minimum number of individuals, based on the dental remains, is confirmed as at least 5, but most probably 6, although with a different allocation of teeth to individual specimens. The age at death of the six individuals has also been reassessed, indicating the presence of two infants, two young adults and two mature adults

Human deciduous teeth from the Middle Stone Age layers of Sibudu Cave (South Africa)

Abstract: In the African Pleistocene, the fossil evidence for early Homo sapiens populations is still relatively limited. Here we present two additional specimens (two deciduous teeth) recovered from the Middle Stone Age (MSA) deposits of Sibudu Cave (KwaZulu‐Natal, South Africa). We describe their morphology and metrics, using three‐dimensional models of the teeth obtained from high‐resolution micro‐CT images. The first specimen is a Ldm1 (HUM. TO 1) recovered in the BS5 layer dated 77.3 ± 2.7 ka, and associated with stone tools assigned to the “pre‐Still Bay” assemblage. The other specimen is a Rdi1 (HUM. TO 2) coming from the Pinkish Grey Sand (PGS) layer, dated 64.7±2.3 ka, and associated with a Howieson’s Poort industry. Both teeth are well preserved, with minor post mortem cracks not affecting the overall morphology, and they comprise the intact, worn crown and the remnants of the roots, naturally resorbed. A large carious lesion occupies most of the distal face and part of the occlusal surface in the Ldm1; also a chip of enamel is missing from the disto‐buccal corner. In the Rdi1 average enamel thickness and relative enamel thickness values have been measured. For both teeth, we compared mesiodistal (MD) and bucco‐lingual (BL) diameters with those of other Late Pleistocene deciduous teeth and extant Homo sapiens. The analysis has shown that the teeth are comparable in size with the other MSA specimens described in the literature

Ancient genomes reveal a high diversity of Mycobacterium leprae in medieval Europe.

Studying ancient DNA allows us to retrace the evolutionary history of human pathogens, such as Mycobacterium leprae, the main causative agent of leprosy. Leprosy is one of the oldest recorded and most stigmatizing diseases in human history. The disease was prevalent in Europe until the 16th century and is still endemic in many countries with over 200,000 new cases reported annually. Previous worldwide studies on modern and European medieval M. leprae genomes revealed that they cluster into several distinct branches of which two were present in medieval Northwestern Europe. In this study, we analyzed 10 new medieval M. leprae genomes including the so far oldest M. leprae genome from one of the earliest known cases of leprosy in the United Kingdom-a skeleton from the Great Chesterford cemetery with a calibrated age of 415-545 C.E. This dataset provides a genetic time transect of M. leprae diversity in Europe over the past 1500 years. We find M. leprae strains from four distinct branches to be present in the Early Medieval Period, and strains from three different branches were detected within a single cemetery from the High Medieval Period. Altogether these findings suggest a higher genetic diversity of M. leprae strains in medieval Europe at various time points than previously assumed. The resulting more complex picture of the past phylogeography of leprosy in Europe impacts current phylogeographical models of M. leprae dissemination. It suggests alternative models for the past spread of leprosy such as a wide spread prevalence of strains from different branches in Eurasia already in Antiquity or maybe even an origin in Western Eurasia. Furthermore, these results highlight how studying ancient M. leprae strains improves understanding the history of leprosy worldwide

Ancient genomes reveal a high diversity of Mycobacterium leprae in medieval Europe.

Studying ancient DNA allows us to retrace the evolutionary history of human pathogens, such as Mycobacterium leprae, the main causative agent of leprosy. Leprosy is one of the oldest recorded and most stigmatizing diseases in human history. The disease was prevalent in Europe until the 16th century and is still endemic in many countries with over 200,000 new cases reported annually. Previous worldwide studies on modern and European medieval M. leprae genomes revealed that they cluster into several distinct branches of which two were present in medieval Northwestern Europe. In this study, we analyzed 10 new medieval M. leprae genomes including the so far oldest M. leprae genome from one of the earliest known cases of leprosy in the United Kingdom-a skeleton from the Great Chesterford cemetery with a calibrated age of 415-545 C.E. This dataset provides a genetic time transect of M. leprae diversity in Europe over the past 1500 years. We find M. leprae strains from four distinct branches to be present in the Early Medieval Period, and strains from three different branches were detected within a single cemetery from the High Medieval Period. Altogether these findings suggest a higher genetic diversity of M. leprae strains in medieval Europe at various time points than previously assumed. The resulting more complex picture of the past phylogeography of leprosy in Europe impacts current phylogeographical models of M. leprae dissemination. It suggests alternative models for the past spread of leprosy such as a wide spread prevalence of strains from different branches in Eurasia already in Antiquity or maybe even an origin in Western Eurasia. Furthermore, these results highlight how studying ancient M. leprae strains improves understanding the history of leprosy worldwide