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. 2018 Mar 8;555(7695):190-196.
doi: 10.1038/nature25738. Epub 2018 Feb 21.

The Beaker phenomenon and the genomic transformation of northwest Europe

Iñigo Olalde  1 Selina Brace  2 Morten E Allentoft  3 Ian Armit  4 Kristian Kristiansen  5 Thomas Booth  2 Nadin Rohland  1 Swapan Mallick  1   6   7 Anna Szécsényi-Nagy  8 Alissa Mittnik  9   10 Eveline Altena  11 Mark Lipson  1 Iosif Lazaridis  1   6 Thomas K Harper  12 Nick Patterson  6 Nasreen Broomandkhoshbacht  1   7 Yoan Diekmann  13 Zuzana Faltyskova  13 Daniel Fernandes  14   15   16 Matthew Ferry  1   7 Eadaoin Harney  1 Peter de Knijff  11 Megan Michel  1   7 Jonas Oppenheimer  1   7 Kristin Stewardson  1   7 Alistair Barclay  17 Kurt Werner Alt  18   19   20 Corina Liesau  21 Patricia Ríos  21 Concepción Blasco  21 Jorge Vega Miguel  22 Roberto Menduiña García  22 Azucena Avilés Fernández  23 Eszter Bánffy  24   25 Maria Bernabò-Brea  26 David Billoin  27 Clive Bonsall  28 Laura Bonsall  29 Tim Allen  30 Lindsey Büster  4 Sophie Carver  31 Laura Castells Navarro  4 Oliver E Craig  32 Gordon T Cook  33 Barry Cunliffe  34 Anthony Denaire  35 Kirsten Egging Dinwiddy  17 Natasha Dodwell  36 Michal Ernée  37 Christopher Evans  38 Milan Kuchařík  39 Joan Francès Farré  40 Chris Fowler  41 Michiel Gazenbeek  42 Rafael Garrido Pena  21 María Haber-Uriarte  23 Elżbieta Haduch  43 Gill Hey  30 Nick Jowett  44 Timothy Knowles  45 Ken Massy  46 Saskia Pfrengle  9 Philippe Lefranc  47 Olivier Lemercier  48 Arnaud Lefebvre  49   50 César Heras Martínez  51   52   53 Virginia Galera Olmo  52   53 Ana Bastida Ramírez  51 Joaquín Lomba Maurandi  23 Tona Majó  54 Jacqueline I McKinley  17 Kathleen McSweeney  28 Balázs Gusztáv Mende  8 Alessandra Modi  55 Gabriella Kulcsár  24 Viktória Kiss  24 András Czene  56 Róbert Patay  57 Anna Endrődi  58 Kitti Köhler  24 Tamás Hajdu  59   60 Tamás Szeniczey  59 János Dani  61 Zsolt Bernert  60 Maya Hoole  62 Olivia Cheronet  14   15 Denise Keating  63 Petr Velemínský  64 Miroslav Dobeš  37 Francesca Candilio  65   66   67 Fraser Brown  30 Raúl Flores Fernández  68 Ana-Mercedes Herrero-Corral  69 Sebastiano Tusa  70 Emiliano Carnieri  71 Luigi Lentini  72 Antonella Valenti  73 Alessandro Zanini  74 Clive Waddington  75 Germán Delibes  76 Elisa Guerra-Doce  76 Benjamin Neil  38 Marcus Brittain  38 Mike Luke  77 Richard Mortimer  36 Jocelyne Desideri  78 Marie Besse  78 Günter Brücken  79 Mirosław Furmanek  80 Agata Hałuszko  80 Maksym Mackiewicz  80 Artur Rapiński  81 Stephany Leach  82 Ignacio Soriano  83 Katina T Lillios  84 João Luís Cardoso  85   86 Michael Parker Pearson  87 Piotr Włodarczak  88 T Douglas Price  89 Pilar Prieto  90 Pierre-Jérôme Rey  91 Roberto Risch  83 Manuel A Rojo Guerra  92 Aurore Schmitt  93 Joël Serralongue  94 Ana Maria Silva  95 Václav Smrčka  96 Luc Vergnaud  97 João Zilhão  85   98   99 David Caramelli  55 Thomas Higham  100 Mark G Thomas  13 Douglas J Kennett  101 Harry Fokkens  102 Volker Heyd  31   103 Alison Sheridan  104 Karl-Göran Sjögren  5 Philipp W Stockhammer  46   105 Johannes Krause  105 Ron Pinhasi  14   15 Wolfgang Haak  105   106 Ian Barnes  2 Carles Lalueza-Fox  107 David Reich  1   6   7
Affiliations

The Beaker phenomenon and the genomic transformation of northwest Europe

Iñigo Olalde et al. Nature. .

Erratum in

  • Erratum: The Beaker phenomenon and the genomic transformation of northwest Europe.
    Olalde I, Brace S, Allentoft ME, Armit I, Kristiansen K, Booth T, Rohland N, Mallick S, Szécsényi-Nagy A, Mittnik A, Altena E, Lipson M, Lazaridis I, Harper TK, Patterson N, Broomandkhoshbacht N, Diekmann Y, Faltyskova Z, Fernandes D, Ferry M, Harney E, de Knijff P, Michel M, Oppenheimer J, Stewardson K, Barclay A, Alt KW, Liesau C, Ríos P, Blasco C, Miguel JV, García RM, Fernández AA, Bánffy E, Bernabò-Brea M, Billoin D, Bonsall C, Bonsall L, Allen T, Büster L, Carver S, Navarro LC, Craig OE, Cook GT, Cunliffe B, Denaire A, Dinwiddy KE, Dodwell N, Ernée M, Evans C, Kuchařík M, Farré JF, Fowler C, Gazenbeek M, Pena RG, Haber-Uriarte M, Haduch E, Hey G, Jowett N, Knowles T, Massy K, Pfrengle S, Lefranc P, Lemercier O, Lefebvre A, Martínez CH, Olmo VG, Ramírez AB, Maurandi JL, Majó T, McKinley JI, McSweeney K, Mende BG, Modi A, Kulcsár G, Kiss V, Czene A, Patay R, Endrődi A, Köhler K, Hajdu T, Szeniczey T, Dani J, Bernert Z, Hoole M, Cheronet O, Keating D, Velemínský P, Dobeš M, Candilio F, Brown F, Fernández RF, Herrero-Corral AM, Tusa S, Carnieri E, Lentini L, Valenti A, Zanini A, Waddington C, Delibes G, Guerra-Doce E, Neil B, Brittain M, Luke M, Mortimer R, Desideri J, Besse M, … See abstract for full author list ➔ Olalde I, et al. Nature. 2018 Mar 21;555(7697):543. doi: 10.1038/nature26164. Nature. 2018. PMID: 29565364

Abstract

From around 2750 to 2500 bc, Bell Beaker pottery became widespread across western and central Europe, before it disappeared between 2200 and 1800 bc. The forces that propelled its expansion are a matter of long-standing debate, and there is support for both cultural diffusion and migration having a role in this process. Here we present genome-wide data from 400 Neolithic, Copper Age and Bronze Age Europeans, including 226 individuals associated with Beaker-complex artefacts. We detected limited genetic affinity between Beaker-complex-associated individuals from Iberia and central Europe, and thus exclude migration as an important mechanism of spread between these two regions. However, migration had a key role in the further dissemination of the Beaker complex. We document this phenomenon most clearly in Britain, where the spread of the Beaker complex introduced high levels of steppe-related ancestry and was associated with the replacement of approximately 90% of Britain's gene pool within a few hundred years, continuing the east-to-west expansion that had brought steppe-related ancestry into central and northern Europe over the previous centuries.

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Conflict of interest statement

The authors declare no competing financial interests.

Figures

Extended Data Figure 1
Extended Data Figure 1. Beaker complex artefacts
a, ‘All-Over-Cord’ Beaker from Bathgate, West Lothian, Scotland. Photo: ãNational Museums Scotland. b, Beaker Complex grave goods from La Sima III barrow, Soria, Spain. The set includes Beaker pots of the so-called ‘Maritime style’. Photo: Junta de Castilla y León, Archivo Museo Numantino, Alejandro Plaza.
Extended Data Figure 2
Extended Data Figure 2. Ancient individuals with previously published genome-wide data used in this study
a, Sampling locations. b, Time ranges. W/E/S/CHG, Western/Eastern/Scandinavian/Caucasus hunter-gatherers; E, Early; M, Middle; L, Late; N, Neolithic; CA, Copper Age; BA, Bronze Age. Map data from the R package maps.
Extended Data Figure 3
Extended Data Figure 3. Population structure
a, Principal component analysis of 990 present-day West Eurasian individuals (grey dots), with previously published (pale yellow) and new ancient samples projected onto the first two principal components. b, ADMIXTURE clustering analysis with k=8 showing ancient individuals. W/E/S/CHG, Western/Eastern/Scandinavian/Caucasus hunter-gatherers; E, Early; M, Middle; L, Late; N, Neolithic; CA, Copper Age; BA, Bronze Age.
Extended Data Figure 4
Extended Data Figure 4. Hunter-gatherer affinities in Neolithic/Copper Age Europe
Differential affinity to hunter-gatherer individuals (LaBraña1 from Spain and KO1 from Hungary) in European populations before the emergence of the Beaker Complex. See Supplementary Information, section 8 for mixture proportions and standard errors computed with qpAdm. E, Early; M, Middle; L, Late; N, Neolithic; CA, Copper Age; BA, Bronze Age; N_Iberia, Northern Iberia; C_Iberia, Central Iberia.
Extended Data Figure 5
Extended Data Figure 5. Modelling the relationships between Neolithic populations
a, Admixture graph fitting a Test population as a mixture of sources related to both Iberia_EN and Hungary_EN. b, Likelihood distribution for models with different proportions of the source related to Iberia_EN (green admixture edge in (a)) when Test is England_N, Scotland_N or France_MLN. E, Early; M, Middle; L, Late; N, Neolithic.
Extended Data Figure 6
Extended Data Figure 6. Genetic affinity between Beaker Complex-associated individuals from southern England and the Netherlands
a, f-statistics of the form f4(Mbuti, Test; BK_Netherlands_Tui, BK_England_SOU). Negative values indicate that Test is closer to BK_Netherlands_Tui than to BK_England_SOU, and the opposite for positive values. Error bars represent ±3 standard errors. b, Outgroup-f3 statistics of the form f3(Mbuti; BK_England_SOU, Test) measuring shared genetic drift between BK_England_SOU and other Beaker Complex-associated groups. Error bars represent ±1 standard errors. Number of individuals for each group is given in parentheses. BK_Netherlands_Tui, Beaker-associated individuals from De Tuithoorn, Oostwoud, the Netherlands; BK_England_SOU, Beaker-associated individuals from southern England. See Supplementary Table 1 for individuals associated to each population label.
Extended Data Figure 7
Extended Data Figure 7. Derived allele frequencies at three SNPs of functional importance
Error bars represent 1.9-log-likelihood support interval. The red dashed lines show allele frequencies in the 1000 Genomes GBR population (present-day people from Great Britain). Sample sizes are 50, 98, and 117 for Britain Neolithic, Britain CA-BA and Central European BC, respectively. BC, Beaker Complex; CA, Copper Age; BA, Bronze Age.
Figure 1
Figure 1. Spatial, temporal, and genetic structure of individuals in this study
a, Geographic distribution of samples with new genome-wide data. Random jitter was added for sites with multiple individuals. Map data from the R package maps. b, Approximate time ranges for samples with new genome-wide data. Sample sizes are given next to each bar. c, Principal component analysis of 990 present-day West Eurasian individuals (grey dots), with previously published (pale yellow) and new ancient samples projected onto the first two principal components. This figure is a zoom of Extended Data Fig. 3a. See Methods for abbreviations of population names.
Figure 2
Figure 2. Investigating the genetic makeup of Beaker Complex individuals
a, Proportion of Steppe-related ancestry (shown in black) in Beaker Complex-associated groups, computed with qpAdm under the model Steppe_EBA + Anatolia_N + WHG. The area of the pie is proportional to the number of individuals (shown inside the pie if more than one). Map data from the R package maps. b, f-statistics of the form f4(Mbuti, Test; Iberia_EN, LBK_EN) computed for European populations (number of individuals for each group is given in parentheses) before the emergence of the Beaker Complex (Supplementary Information section 7). Error bars represent ±1 standard errors. c, Testing different populations as a source for the Neolithic ancestry component in Beaker Complex individuals. The table shows the P-values (highlighted if >0.05) for the fit of the model: Steppe_EBA + Neolithic/Copper Age source population.
Figure 3
Figure 3. Population transformation in Britain associated with the arrival of the Beaker Complex
Modelling Neolithic, Copper and Bronze Age (including Beaker Complex-associated) individuals from Britain as a mixture of continental Beaker Complex-associated individuals (red) and the Neolithic population from Britain (blue). Each bar represents genome-wide mixture proportions for one individual. Individuals are ordered chronologically and included in the plot if represented by more than 100,000 SNPs. Circles indicate the Y-chromosome haplogroup for male individuals.

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