More light shed on use of plants by Homo neanderthalensis

The ecology of Neanderthals is a pressing question in the study of hominin evolution. Diet appears to have played a prominent role in their adaptation to Eurasia. Based on isotope and zooarchaeological studies, Neanderthal diet has been reconstructed as heavily meat-based and generally similar across different environments. This image persists, despite recent studies suggesting more plant use and more variation. However, we have only a fragmentary picture of their dietary ecology, and how it may have varied among habitats, because we lack broad and environmentally representative information about their use of plants and other foods. To address the problem, we examined the plant microremains in Neanderthal dental calculus from five archaeological sites representing a variety of environments from the northern Balkans, and the western, central and eastern Mediterranean. The recovered microremains revealed the consumption of a variety of non-animal foods, including starchy plants. Using a modeling approach, we explored the relationships among microremains and environment, while controlling for chronology. In the process, we compared the effectiveness of various diversity metrics and their shortcomings for studying microbotanical remains, which are often morphologically redundant for identification. We developed Minimum Botanical Units as a new way of estimating how many plant types or parts are present in a microbotanical sample. In contrast to some previous work, we found no evidence that plant use is confined to the southern-most areas of Neanderthal distribution. Although interpreting the eco-geographic variation is limited by the incomplete preservation of dietary micro remains, it is clear that plant exploitation was a widespread and deeply rooted Neanderthal subsistence strategy, even if they were predominately game hunters. Given the limited dietary variation across Neanderthal range in time and space in both plant and animal food exploitation, we argue that vegetal consumption was a feature of a generally static dietary niche.

Dental calculus indicates widespread plant use within the stable Neanderthal dietary niche

Robert C. Power, Domingo C. Salazar-García, Mauro Rubini, Andrea Darlas, Katerina Harvati, Michael Walker, Jean-Jacques Hublin, Amanda G.Henry

DOI: 10.1016/j.jhevol.2018.02.009

The First Human Epidemic: Late Pleistocene Origin?

Current models of infectious disease in the Pleistocene tell us little about the pathogens that would have infected Neanderthals (Homo neanderthalensis). High quality Altai Neanderthal and Denisovan genomes are revealing which regions of archaic hominin DNA have persisted in the modern human genome. A number of these regions are associated with response to infection and immunity, with a suggestion that derived Neanderthal alleles found in modern Europeans and East Asians may be associated with autoimmunity. Independent sources of DNA-based evidence allow a re-evaluation of the nature and timing of the first epidemiologic transition. The paradigm of the first epidemiologic transmission, the hypothesis that epidemic disease did not occur until the transition to agriculture, with larger, denser and more sedentary populations, has been essentially unchallenged since the 1970s. Our views of the infectious disease environment of the Pleistocene period are heavily influenced by skeletal data and studies of contemporary hunter-gatherers. New genetic data – encompassing both hosts and pathogens – has the power to transform our view of the infectious disease landscape experienced by Neanderthals in Europe, and the anatomically modern humans (AMH) with whom they came into contact. The Pleistocene hominin environment cannot be thought of as free from infectious disease. It seems likely that the first epidemiologic transition, envisaged as part of the package of the Holocene farming lifestyle, may be fundamentally different in pace or scope than has previously been suggested. This paper demonstrates how high quality genomic data sets can be used to address questions arisingfrom the ecological context that shaped the co-evolutionary relationship we share with infectious diseases. We analyse the evidence for infectious disease in Neanderthals, beginning with that of infection-related skeletal pathologies in the archaeological record, and then consider the role of infection in hominin evolution. We have synthesised current models on the chronology of emergence of notable European disease packages and analyse what implications this evidence has for the classical model of the first epidemiologic transition. Using emerging data from Neanderthal palaeogenomics and combining this with fossil and archaeological information we re-examine the impact of infectious diseases on human populations from an evolutionary context. These palaeogeneticists argue that the first epidemiologic transition in Eurasia was not as tightly tied to the onset of the Holocene as has previously been assumed. There is clear evidence to suggest that this transition began before the appearance of agriculture and occurred over a timescale of tens of thousands of years. We suggest that the epidemiological transition was not, as has been thought since the 1970s, a phenomenon of the human shift to sedentary agriculture during the Holocene but a much older and more complex process that involved at least two species of humans. The origin of resistance to infectious disease has a much deeper timeframe and is highlighted by the ingression of Neanderthal DNA into modern human lineages. The transfer of pathogens between human species may also have played a role in the extinction of the Neanderthals. Our analysis of the genomes of archaic hominins provides evidence of pathogens acting as a population-level selection pressure, causing changes in genomes that were passed on to descendants and preserved in the genomes of modern Eurasians. the analysis of ancient genomes demonstrates that human behavioural patterns (in this case a shift to agricultural subsistence) should not be used as an ecological proxy to explain shifting trends in the co-evolutionary relationship between pathogens and human populations.

This work is available on BioRxiv: http://dx.doi.org/10.1101/017343

Acknowledgements: Rob Foley, Marta Lahr and the members of the Human Evolutionary Science Discussion Group at the University
of Cambridge. Funding for this research was provided by King’s College Cambridge and UCL.

Gorjanović-Kramberger Hypothesis: Took 99 Years, But We Finally Tested It

You meet Homo neanderthalensis in a dark alley……………….What do you do?

Homo neanderthalensis is one of the best understood species of hominin today. One that lasted many hundreds of thousands of years throughout Europe. Despite what we know through the lens of science, there is still much that we want to know about this species of human. Interrogating the subtle pieces of evidence is the task of palaeoanthropologists, archaeologists, palaeoenvironmental scientists throughout the world. Contrary to what you may see on your average human evolution documentary, the kind of research conducted can be much more subtle. Here I will draw your attention to a difficult question. If we could fill the Great Hall of the South Kensington Museum with a few hundred individuals of our extinct cousin, what differences would we see in the upper chest and neck. The answer to that, at the beginning of 2015: We are not happy that we really know enough to give an answer.

Range_of_Homo_neanderthalensis
Range of Homo neanderthalensis

H. neanderthalensis is a well represented species of human in the fossil record, but the post-cranial anatomy is less well accounted for than the skulls. Not ideal for an investigation into the chest and abdominal regions of the human body. Nevertheless, it is vital we exhaustively examine what we have, to reveal potential clues to the kind of morphology these populations once exhibited. To that end, ten palaeobiologists from various Spanish academic institutions presented evidence that may be useful here. The mechanics of the breathing system, constrained by the rib cage and not the evolution of the species, is the focus here. Research continues to be a work in progress, new technologies arrive and they help further our understanding of the past. This research is no exception. Two year into the new millennium a new form of analysis that gauged quantity within a structure was applied to a collection of isolated ribs from an individual codenamed Shanidar 3. This individual had a more splayed lower rib cage compared to the more barrel-like form of our lower rib cage. Thus started a series of papers that suggested the lower rib cage of Homo neanderthalensis was generally less like ours. Comparatively less investigative research has been given to the upper end of the rib cage. This latest academic paper sets out to help understand just that.

Title and Authors of the Paper in Question
Title and Authors of the Paper in Question
640px-Krapina_-_Dragutin_Gorjanovic_Kramberger
Dragutin Gorjanović-Kramberger (1856 – 1936)

In 1906 and a time when ancient humans were Anti or Post Diluvian Era (Noah’s Great Flood), Dragutin Gorjanović-Kramberger suggested that the superior ribs are an important facet of an upper thoracic orchestra of components, that together control upper thoracic breathing, separate from diaphragmatic breathing. It was not until 2015 that this hypothesis was put to the test on six hominin first-ribs from the cave site of El Sidrón, Asturias, northern Spain. The six first-rib fragments may represent, at most, four individuals. The first step was to identify the bone fragments and place them in their correct anatomical position. Below is a re-organisation of the information given about the sample itself. The first-rib of Kebara 2 was found to be similar in shape space and form space (both terms used in a statistical analysis of shape, known as Procrustes Least Squares (PLS)) to SD-1767 and SD-1699, indeed H. neanderthalensis exhibits straighter first-ribs than modern day Homo sapiens. What could this mean? The scalene muscles are the ones that give your neck, its shape. They run from the Rib 1 and Rib 2 up the side of your neck attaching to the vertebrae. Alteration in shape of the first ribs, and the attached muscles will have to operate differently, but may help explain the differences we see between H. sapiens and H. neanderthalensis. The principle component analysis (PCA) reveals some overlap in the linearity of the rib shaft. Such results are reflected in analysis of the specimens of Krapina Cave, Croatia and ATD6-108 representing Homo antecessor, from Gran Dolina Cave, Atapuerca, Spain. So, the straightness of the first-ribs may affect the movement of the upper torso during breathing.

Juvenile 1: SD-2148 (Right) and SD-2172 (Left)

Juvenile 2: SD-417 (Left) and SD-1225 (Right)

Large Adolescent / Small Adult: SD-1767 (Left)

Large Adult: SD-1699 (Right)

Looking at the juveniles, it is important to understand costal cartilage development. Understanding adult H. neanderthalensis individuals is easier, as there are more post-cranial fossils, but the El Sidrón hominins will be useful in understanding the ontogeny of costal cartilage in future fossil ribs of  juveniles. The El Sidrón juveniles confirm a tighter upper chest for H. neanderthalensis. The first-ribs are smaller, but feature larger attachments at the rib heads, whereas the lower ribs have smaller attachment points. Therefore, a H. neanderthalensis individual, exhibited a smaller upper torso, which was further from the cranium thanks to the slightly longer neck vertebrae. First-ribs that are straighter would have to project out from the skeleton more and Gorjanović-Kramberger proposed that the rest of the rib-cage would project outward, just as much. The scientific team added to this, that a change in the first ribs would in turn affect the rest of the rib-cage, because the ribs are latched together with intercostal muscle, preventing individual ribs from varying in shape, that ultimately allows coordination of muscle, chest wall and breathing action. Upper ribs connect directly with the sternum and so, result in distinctive rib shape compared with the lower thorax.

Association of Intercostal Muscle and Rib Bone
Association of Intercostal Muscle and Rib Bone

To summarise, the first ribs appear to determine the shape of the upper thorax ribs, but straightness of the first rib is linked with the straightness of the upper ribs. Together, this suggests the existence of different rib shape and functions between the upper and lower thorax. When you look at a particular fossil specimen, it is important you are aware of what bones, muscles, cartilage was associated with it. They all interact in subtle ways which we are piecing together in hominins, with the variety in body forms available going back 7 million years. In examination of the monophyly of Paranthropus, cladistical statistics showed us that the skeletal points used, should not be linked with eachother. An example of that, would be the masticatory system in Paranthropus comprising numerous points, all interacting with one another. This is a shame because the crania and mandibles are predominantly all we have of that genus. Currently, most are happy that Paranthropus boisei, Paranthropus aethiopicus and Paranthropus robustus are part of the same family – they are monophyletic. The rib cage, is similar to the masticatory system but it is a single unit with two functions, one  is upper thoracic respiration and the other is diaphragmatic respiration. H. neanderthalensis evolved a more restrictive respiratory system and highly developed arm muscles, evolutionarily more important for the condition in which it lived. So, if you were to meet our ancient ancestor in a dark alley, what should you do? It would have been prone to breathlessness, but could rearrange your face easier. Moral of the story, RUN!

The costal remains of the El Sidrón Neanderthal site (Asturias, northern Spain) and their importance for understanding Neanderthal thorax morphology

Social Media Destinations:

Facebook

Twitter

Google+

Academia.edu

SoundCloud

The Stunning Architecture of the Leaning Tower of Pisa, Italy

At nearly 56 metres high, the Leaning Tower of Pisa, Italy is the most famous tourist attraction in Tuscany. At the top it currently leans nearly 4 metres from the upright position.

Timeline:
A.D. 1173, the foundations of the tower were laid.

A.D. 1178 work halted at the 2nd floor at which point it began to lean.

A.D. 1272: work resumed at the tower until A.D. 1284

A.D. 1319: Work resumed at the tower to the 7th floor until the final completion of the Bell Chamber in A.D. 1372.