|Common name||Cheddar Man|
|Age||9th millennium BC|
|Place discovered||Gough's Cave|
Cheddar Man is a human male fossil found in Gough's Cave in Cheddar Gorge, Somerset, England. The skeletal remains date to around the mid-to-late 9th millennium BC, corresponding to the Mesolithic period, and it appears that he died a violent death. A large crater-like lesion just above the skull's right orbit suggests that the man may have also been suffering from a bone infection.
Analysis of his nuclear DNA indicates that he was a typical member of the Western European hunter-gatherer population at the time, with a most likely inferred phenotype of blue-green eyes, dark brown or black hair, and dark or dark-to-black skin, with no genetic adaption for lactase persistence into adulthood.
The near-complete skeleton, an adult male who probably died in his early twenties, was discovered in 1903 by labourers digging a drainage ditch. No grave goods have been reliably associated with the skeleton. It is likely that Cheddar Man was moved to the cave after death as part of what may have been a Mesolithic funerary practice, although it is also possible that he simply died in situ.
Cheddar Man has been directly radiocarbon dated on two separate occasions, giving calibrated dates of 8540-7990 BC and 8470-8230 BC.
Cheddar Man was relatively small compared to modern Europeans, with an estimated stature of around 1.66 metres (5 ft 5 in), and weighing around 66 kilograms (146 lb). Proportionally, he is in most respects similar to modern Europeans, and may be described as 'cold-adapted', but with a high crural index (thigh length to leg length ratio) which is much higher than the modern European average and higher even than the modern sub-Saharan African average, and a high tibia length-to-trunk height ratio similar to modern North Africans.
Nuclear DNA was extracted from the petrous part of the temporal bone by a team from the Natural History Museum in 2018. While the relevant genetic markers on the Cheddar Man genome have low sequencing coverage, limiting the accuracy of the predictions, they suggest (based on their associations in modern populations whose phenotypes are known) that he most likely had intermediate (blue-green) eye colour, dark brown or black curly or wavy hair, and dark or dark-to-black skin, with no derived allele for lactase persistence.[a] These features are typical of the Western European population of the time, now known as Western Hunter-Gatherers, another example being Loschbour man discovered in Luxembourg. This population forms about 10%, on average, of the ancestry of Britons without a recent family history of immigration. Brown eyes, lactose tolerance, and light skin are common in the modern population of the area. These genes came from later immigration, most of it ultimately from two major waves, the first of Neolithic farmers from the Near East, another of Bronze Age pastoralists, most likely speakers of Indo-European languages, from the Pontic steppe.
About 85% of his ancestry can be modelled as coming from the ~14,000–7,000-year-old Villabruna genetic cluster, and only c. 15% from the Goyet Q2 cave cluster whose genes are found in association with the Late Upper Palaeolithic Magdalenian culture. He is not closely related to the earlier Magdalenian individuals found in the same cave, whose ancestry is entirely from the Goyet cluster. The genomes of all British Mesolithic individuals sequenced to date other than Cheddar Man can be modelled as only Villabruna-related (WHG) ancestry, without additional Goyet-related admixture.
Cheddar Man's Y-DNA belonged to an ancient sister branch of modern I2-L38 (I2a2). The I2a2 subclade is still extant in males of the modern British Isles and across other parts of Europe. The mitochondrial DNA of Cheddar Man was discovered to be haplogroup U5b1 by a Natural History Museum study in 2018 using next generation sequencing. Some 65% of western European Mesolithic hunter-gatherers had haplogroup U5; today it is widely distributed, at lower frequencies, across western Eurasia and northern Africa. In 1996, Bryan Sykes of the University of Oxford first sequenced the mitochondrial DNA from one of Cheddar Man's molars as U5a using PCR testing. The difference between the older result and the 2018 Natural History Museum result was attributed to the use of older PCR technology and possible contamination.
In popular culture
Soon after the discovery of the skeleton, Cheddar Man was heralded as the 'first Englishman' with an initially proposed age of 40,000-80,000 years, and became part of a discourse of British (or English) nationalism and cultural heritage.
The analysis of Cheddar Man's mitochondrial DNA by Bryan Sykes in 1996 was broadcast on a regional television programme in the UK, Once Upon a Time in the West. The programme emphasised the connection between Cheddar Man and a history teacher from a local school, both of whom belonged to mitochondrial DNA haplogroup U5, although this cannot demonstrate a direct connection between Cheddar Man and this individual, and many people with the same mtDNA haplogroup could probably be found even within the local area. The programme generated coverage in national and international media, which focused mainly on the supposed relationship between Cheddar Man and the local history teacher, and failed to emphasise that mitochondrial DNA is only passed on through the mother, and makes up only a small proportion of an individual's genome.
In 2018 the publication of the genetics study by Brace et al. and subsequent facial reconstruction of a dark-skinned Cheddar Man resulted in widespread media coverage which again described Cheddar Man as the 'first Brit', and led to discussion on social media involving themes of immigration, national identity, race, and Brexit. The study was interpreted both as an anti-racist response to anti-immigration arguments and as left-wing academic propaganda. Cheddar Man's predicted dark skin colour and the expertise of the authors of the study have been disputed on social media.
- These predictions were obtained using a multinomial logistic regression model based on a panel of 36 carefully selected SNPs with a low sensitivity of 0.26 for classifying intermediate skin (compared to 0.99 and 0.90 for white and black skin, respectively). The accuracy of the model used could be further improved with "additional (but currently unknown) SNP predictors once identified via future GWAS".
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- Brace, Selina; Diekmann, Yoan; Booth, Thomas J.; Faltyskova, Zuzana; Rohland, Nadin; Mallick, Swapan; Ferry, Matthew; Michel, Megan; Oppenheimer, Jonas; Broomandkhoshbacht, Nasreen; Stewardson, Kristin; Walsh, Susan; Kayser, Manfred; Schulting, Rick; Craig, Oliver E.; Sheridan, Alison; Pearson, Mike Parker; Stringer, Chris; Reich, David; Thomas, Mark G.; Barnes, Ian (2019), "Ancient genomes indicate population replacement in Early Neolithic Britain", Nature Ecology & Evolution, 3 (5): 765–771, doi:10.1038/s41559-019-0871-9, PMC 6520225, PMID 30988490 Supplementary Material (p.18-19): "This individual has light or blue/green eye colour, it is not light blue, there are elements of brown/yellow in the eye to give a proposed perceived green colour. Better coverage at the low sequenced marker would clarify this but blue/hazel cannot be ruled out. It is certainly not a brown eyed or clear blue-eyed individual... Skin pigmentation [assumptions about missing information omitted] The following range for skin pigmentation prediction is possible for this individual with these parameters:... Intermediate 0.152 - 0.038 Dark-Black 0.848 - 0.962 Final prediction: Dark/Dark-to-Black skin If we omit the three missing alleles, our tool produces 0.752 and 0.248 probabilities for the intermediate and dark-black category respectively, changing the prediction ranges to 0.752- 0.038 and 0.248-0.962. However, note that this completely removes the locus from the prediction model; hence the prediction will not perform optimally (how the prediction model was made). It is therefore best to have some allele present to infer the most probable range for Cheddar Man and we derive the ranges above from the extreme allele constellations only. Explanation: The missing loci certainly impact on this prediction; however, utilizing the input of all ancestral alleles is the preferred option over the use of the derived alleles at these loci – hence 0.152 for intermediate and 0.848 for Dark-to-Black would be the most probable profile. That being said a broad range is present in both the intermediate and dark-black categories due to the missing loci. Also, this effect of skipping a skin pigmentation prediction category with regards probability values, tends to be observed more often in admixed individuals. What is important to note is the input of the dark-black prediction is significant on the intermediate category and therefore it is acceptable to propose a dark complexion individual over an intermediate/light prediction even though the intermediate range is present. It is unlikely that this individual has the darkest possible pigmentation, but it cannot be ruled out. Better sequencing coverage would clarify to what degree this individual has a dark complexion."
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