Previous mitochondrial DNA analyses on ancient European remains have suggested that the current distribution of haplogroup H was modeled by the expansion of the Bell Beaker culture (ca 4,500–4,050 years BP) out of Iberia during the Chalcolithic period. However, little is known on the genetic composition of contemporaneous Iberian populations that do not carry the archaeological tool kit defining this culture. Here we have retrieved mitochondrial DNA (mtDNA) sequences from 19 individuals from a Chalcolithic sample from El Mirador cave in Spain, dated to 4,760–4,200 years BP and we have analyzed the haplogroup composition in the context of modern and ancient populations. Regarding extant African, Asian and European populations, El Mirador shows affinities with Near Eastern groups. In different analyses with other ancient samples, El Mirador clusters with Middle and Late Neolithic populations from Germany, belonging to the Rössen, the Salzmünde and the Baalberge archaeological cultures but not with contemporaneous Bell Beakers. Our analyses support the existence of a common genetic signal between Western and Central Europe during the Middle and Late Neolithic and points to a heterogeneous genetic landscape among Chalcolithic groups.
Citation: Gómez-Sánchez D, Olalde I, Pierini F, Matas-Lalueza L, Gigli E, Lari M, et al. (2014) Mitochondrial DNA from El Mirador Cave (Atapuerca, Spain) Reveals the Heterogeneity of Chalcolithic Populations. PLoS ONE 9(8): e105105. https://doi.org/10.1371/journal.pone.0105105
Editor: Michael Hofreiter, University of York, United Kingdom
Received: March 14, 2014; Accepted: July 18, 2014; Published: August 12, 2014
Copyright: © 2014 Gómez-Sánchez et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. El Mirador consensus sequences are deposited at GenBank under accession numbers KJ1866158–KJ1866180.
Funding: This work is supported by FEDER and Spanish Government Grant BFU2012-34157. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Co-authors C.L.F and D.C. are currently Editorial members of PLOS ONE; this does not alter their adherence to PLOS ONE Editorial policies and criteria.
The evolutionary history of the human settlement of Europe has been shaped by a complex pattern of migrations, driven by the appearance of new socio-economical strategies, cultural innovations and ecological changes . This has created a specific genetic landscape that can be investigated from the analysis of current European populations . However, modern-day genetic diversity provides only indirect evidence about the complex history of past populations.
Agriculture first developed in the Fertile Crescent of West Asia around 12–11,000 years ago, being afterwards developed independently over the next few thousand years in other regions of the planet . The Neolithic shift to agriculture and the domestication of animals involved major demographic changes in the prehistoric populations, facilitating extensive human population growths and subsequent migrations .
Archaeological, anthropological and paleoecological evidence supports the existence of a major demographic change that took place with the arrival of the Neolithic around 9,000 years ago and the disappearance of the hunting and gathering strategy in the European continent after only few thousands of years .
However, the scale and nature of the interactions between local Mesolithic hunter-gatherers and incoming farmers has been a subject of much debate, opinions being divided between those who argue in favour of a population expansion from the Near East into Europe [5–9, amog others], and those who think that the process of ‘neolithisation’ was mainly a spread of ideas that led to the acculturation of the indigenous population ,  with some potential regional variation –.
In recent years, several ancient DNA studies have contributed to this debate by directly analysing ancient human skeletal remains, mainly Neolithic, and comparing their mtDNA composition to those of modern populations from the same area –. The interpretation of the results, obviously quite limited in sample size, has varied from clear genetic continuity from Neolithic to modern times, arrival of new mtDNA types from the Near East and possible hunter-gatherer acculturation in central and northern Europe. In addition, the vast majority of these studies have been restricted to the retrieval by polymerase chain reaction (PCR) of short fragments, predominantly from the hypervariable region-1 (HVR-1) of the mtDNA genome.
With the next-generation sequencing (NGS) technologies it has been possible to retrieve also prehistoric European genomic data. The first of these studies was the 7x coverage genome of the exceptionally well preserved Tyrolean Ice man, Ötzi, dated to about 5,300 years BP . The second one was the partial genomic retrieval of one Neolithic farmer and four Neolithic hunter-gatherers from Scandinavia, dated between 4,400 and 5,300 years BP , , followed by the first retrieval of genomic data from two 7,000 years-old Mesolithic hunter-gatherers from La Braña-Arintero (León, Northwestern Spain) , . These and future autosomal loci studies will enlarge the possibilities of selective and demographic analyses of the European prehistoric populations.
While most of efforts have focused on the Mesolithic-Neolithic transition, more recent periods remain relatively unknown , . Nevertheless, it is likely that the first arrival of farmers was followed by a complex pattern of migrations and also regionalization episodes that can only be uncovered with the analysis of large numbers of individuals from different periods and geographical areas. At present the sequencing of nuclear genomes is a challenging task that will likely be restricted to a limited number of specimens, and thus the mtDNA can still provide valuable, additional information about these complex population processes.
To further investigate the transition between Late Neolithic to the Chalcolithic period, we have analyzed the mtDNA in a recently excavated population from El Mirador cave in Atapuerca, Spain. This site is contemporaneous to the Bell Beaker culture (BBC) but does not carry the diagnostic items of this culture that include the distinctive bell-shaped ceramics and weapons. In fact, the archaeological sites with Bell Beaker remains are very scarce in the Meseta Central of the Iberian Peninsula. It has been suggested  that the Bell Beaker culture represented a population movement from the Iberian Peninsula that could explain the genetic affinities between Central Europe’s Bell Beakers and present-day Iberians. Thus, the analysis of Iberian samples without the archaeological signature of the Bell Beaker culture such as El Mirador is of great interest to unravel the potential heterogeneity of the European Chalcolithic groups and its affinities with extant populations.
Materials and Methods
The cave of El Mirador is located on the southern side of the Sierra de Atapuerca (Burgos, Spain), at an altitude of 1,033 meters above sea level (Fig. 1). The initial archaeological work was carried out in the 1970s by the Edelweiss Speleological Group. Subsequently an area of the cave covering about 20 m2 was affected by clandestine excavators. Later, in 1999, the archaeological fieldwork was resumed, and it is still continuing .
Two different assemblages of human remains were recovered from this site.
- The first human sample was recovered from a 6 m2 survey in an area unaffected by the clandestine workers. Six individuals dated to the Early Bronze Age (4,400–4,100 cal BP) were found. These human remains had been cannibalized and abandoned as rubbish in the Early Bronze Age, being buried later in the Middle or Late Bronze Age .
- After this first survey, in 2009 the fieldwork focused on a small cavity near the wall of the cave, where a collective burial was found. There were some individuals in anatomical position, but the most superficial remains had been disturbed and mixed by the earlier actions of the clandestine excavators. The human remains are associated with pottery without decoration, antler deer tines and fluvial shells. The fieldwork on this burial site is still in progress; however, a minimum number of 22 individuals have been recovered. All of these human remains belong to the Chalcolithic period and have been dated to 4,760–4,200 years cal. BP.
The Chalcolithic samples were left uncleaned until they were sampled for the genetic analysis, to prevent exogenous DNA contamination by handling. The samples analyzed are labelled Mirador 1, 2, 3, 4, 5, 6, 8, 9, 10, 11, 12, 13, 15, 16, 17, 18, 19, 20, 22, 23, 24, 25 and 26 (Table 1) and are deposited at the Institut Català de Paleoecologia Humana i Evolució Social (IPHES) in Tarragona (Spain). No permits were required for the described study.
DNA was extracted from approximately 100 mg of dental root tips following the method described in detail in Lalueza-Fox et. al . The sample was powdered and decalcified overnight with 10 ml 0.5 M EDTA pH 8.0 at 37°C; after centrifugation, the supernatant was removed and the remaining sample was incubated overnight at 50°C with 8.5 ml of water, 1 ml 5% SDS, 0.5 ml 1 M Tris-HCl pH 8.0 and 50 µl of 1 mg/ml Proteinase K. After incubation, the digest was extracted three times, first with phenol, second with phenol-chloroform and third with chloroform, and the aqueous phase was concentrated by dialysis centrifugation using Amicon Centrifugal Filter Devices (Amicon, Millipore). Subsequent purification with silica yielded a final 30 µl extract.
Extraction procedures were performed in an isolated pre-PCR area, adopting the standard precautions of ancient DNA studies –. Multiple extraction and amplification negative controls to monitor for contamination in the reagents were added to each PCR reaction. No amplification products were obtained in these blank PCR controls along the study.
Besides standard precautions in ancient DNA outlined, we followed several additional strategies to support the authenticity of our results. 1) we retrieved endogenous DNA sequences from an animal bone (wolf) from the same site, to ensure that the cave environment was favourable indeed to DNA preservation, 2) we retrieved the same mtDNA haplotype from two teeth belonging to the same individual, 3) we replicated mtDNA sequences of an individual that shares the same mtDNA haplotype with two of the molecular researchers in an independent laboratory (Florence) after sending an additional sample directly from the archaeological institution, and 4) we repeated the amplification and sequencing of potentially rare haplotypes.
In Barcelona, the mtDNA hypervariable region 1 (HVR1) was amplified by polymerase chain reaction (PCR) in two overlapping fragments (L16055-H16218 and L16185-H16378 primers), following a two-steps protocol (27 and 33 cycles of PCR, respectively), in which primers are limited in the first PCR step to avoid the generation of unspecific primer-primer artifacts . In Florence the HVR1 was retrieved in three overlapping fragments (L16995-H16132, L16107-H16247 and L16222-H16327).
In both laboratories, PCR products were subsequently visualized under UV lights in a low-melting point agarose gel. The appropriate bands were excised from the gel, melted at 65° for 20 min, and purified with a silica-based method. Subsequently, the amplification products were cloned in bacteria (TOPO-TA cloning kit, Invitrogen). Resulting white colonies were picked up, amplified with M13 universal primers and sequenced in an ABI3730 capillary sequencer (Applied Biosystems).
The haplogroup frequencies data were classified as described in Brandt et al.  to allow comparison with their results and analysed with R (version 3.1.0). Principal component analyses (PCA) were performed with prcomp function using mtDNA haplogroup diversity (Table S1, S2 and S3) to determine population affinities between El Mirador and prehistoric/present-day European populations. Manhattan distances and 10,000 bootstrap replicates were used to perform hierarchical Ward clustering with pvclust function .
Results and Discussion
From the analysis of 757 clone sequences (Figure S1), we have obtained the mtDNA HVR1 in 19 individuals, accounting for different mtDNA haplogroups and sub-haplogroups previously described in Europe (Table 1). This success rate is remarkably high and could be attributed to the thermal stability favoured by the cave environment, as opposed for instance to open field sites. Other sites at Atapuerca, including Sima de los Huesos, dated to about 400,000 years ago, have yielded endogenous DNA . El Mirador consensus sequences are deposited at GenBank under accession numbers KJ1866158–KJ1866171, KJ1866173–KJ1866176 and KJ1866179–KJ1866180. To differentiate between endogenous substitutions and potential postmortem damage or background contamination (the latter most frequently will emerge as CRS sequences, the most common haplotype in Europeans today) we have replicated at least twice most of the mtDNA fragments, as recommended in Hofreiter et al. . Three samples (Mir17, Mir23 and Mir24) yielded mixed haplotypes in different PCRs and were discarded for subsequent analyses.
Despite the recent retrieval of partial or complete Mesolithic and Neolithic genomes –, the analysis of the mtDNA lineages remains the most widely used marker for reconstructing the human matrilineal population affinities. Recent analyses of partial and complete ancient mtDNA genomes have revealed different events associated to the distribution and diversity of these lineages in modern Europeans , . The analysis of the mtDNA composition along time detected a previously unrecognised major genetic transition between the Early Neolithic and posterior Middle and Late Neolithic periods . While many H haplogroup (the most common in modern Europeans, with frequencies around 40%) lineages were established by the Middle Neolithic period, a subsequent migration movement in the Late Neolithic associated to the Bell Beaker culture added further genetic complexity to the present-day populations. The genetic signature of H haplogroups increased up to 48.3% during the Bell Beaker period with respect to previous European cultures, suggesting a population expansion from Iberia to Central Europe .
However, another recent study based on the analysis of 629,443 single nucleotide polymorphisms (SNPs) from 934 individuals belonging to 53 human populations has uncovered a previously unrecognized signature of Northern European genes into the Iberian Peninsula . Based on the length distribution of the linkage-disequilibrium blocks, it has been possible to date this admixture event to about 4,000 years BP, a figure roughly coincident with the spread of the Bell Beaker culture . They interpret this signal as the result of a reverse migration from central Europe into Iberia after an initial Bell Beaker culture expansion from Iberia. This has been previously hypothesized from archaeological data  but so far has not been observed with ancient genetic data due to the current lack of genetic information from Iberian Bell Beaker groups.
The mtDNA composition of El Mirador is quite unique, and different to that found in other contemporaneous Bell Beaker populations and to present-day Iberians (Figure 2 and 3). This Chalcolithic population displays different mtDNA haplogroups that are currently present at higher frequency in the Near East populations than in continental Europe (e.g., X2, K, T2b); this could explain the clustering of El Mirador with Near Eastern populations in the PCA of modern populations (Figure 3). The Near East signature found here could correspond to the major genetic transition detected by Brandt et al.  between the Early and Late Neolithic and could indicate a subsequent migratory movement into Europe from the Near East, maybe associated to cultural transitions such as Megalithism.
This study: El Mirador (MIR). Published prehistoric cultures : Hunter-gatherer central (HGC), Linear Pottery culture (LBK), Rössen culture (RSC), Schöningen group (SCG), Baalberge culture (BAC), Salzmünde culture (SMC), Bernburg culture (BEC), Corded Ware culture (CWC), Bell Beaker culture (BBC), Unetice culture (UC), Funnel Beaker culture (FBC), Pitted Ware culture (PWC), Hunter-Gatherer south (HGS), (Epi) Cardial (CAR), Neolithic Portugal (NPO), Neolithic Basque Country and Navarre (NBQ), Treilles culture (TRE), Hunter-gatherer east (HGE), Bronze Age Siberia (BAS), Bronze Age Kazakhstan (BAK).
Principal component analysis (PCA) based on mitochondrial haplogroup frequencies of El Mirador (MIR, yellow) and published present-day populations : African/Asian (in blue, from darker to lighter North Africa, Southwest Asia, Central Asia, North Asia and Southwest Asia) and European (in green, from darker to lighter, Central, East, North, South, Southwest and West). For further information about populations, abbreviation and frequencies, see Table S1. The first three principal components display the 54.5% of the total variance.
The clustering of the El Mirador sample with a Salzmünde culture (5,400-5,100/5,025 years BP) population from Germany and the roughly contemporaneous Treilles culture population from France in the PCA of ancient populations (Figure 4 and Figure S2) as well as with the previous Rössen and Baalberge cultures from Germany in the hierarchical Ward clustering (Figure 5) supports the existence of a common genetic signal among Western and Central Europe during the Middle and Late Neolithic. In this context, El Mirador mitochondrial composition may correspond to a previous genetic substratum with a substantial contribution of lineages from the Near East that was not influenced by the expansion of Iberian Bell Beakers, despite being in the same range. Under a chronological perspective (Figure S3) El Mirador supports the continuity of the previous Middle Neolithic genetic composition into the Chalcolithic, at least in non-Bell Beaker groups.
Principal component analysis (PCA) based on mitochondrial haplogroup frequencies of El Mirador (MIR) and 20 published prehistoric cultures : Hunter-gatherer central (HGC), Linear Pottery culture (LBK), Rössen culture (RSC), Schöningen group (SCG), Baalberge culture (BAC), Salzmünde culture (SMC), Bernburg culture (BEC), Corded Ware culture (CWC), Bell Beaker culture (BBC), Unetice culture (UC), Funnel Beaker culture (FBC), Pitted Ware culture (PWC), Hunter-Gatherer south (HGS), (Epi) Cardial (CAR), Neolithic Portugal (NPO), Neolithic Basque Country and Navarre (NBQ), Treilles culture (TRE), Hunter-gatherer east (HGE), Bronze Age Siberia (BAS), Bronze Age Kazakhstan (BAK). Symbols indicate populations from Central Europe (circles), southern Scandinavia (triangles), the Iberian Peninsula (diamonds), and East Europe/Asia (squares). Colour indicates hunter-gatherer (grey), Early Neolithic (brown), Middle Neolithic (orange), and Late Neolithic/EBA (yellow) samples. For further information, see Table S2. The first two components display the 32.1% of the total variance.
Haplogroup frequencies of El Mirador (MIR), hunter-gatherer central (HGC), and nine Mittelelbe-Saale (Saxony-Anhalt region in Germany) cultures  have been used to generate a hierarchical Ward clustering. Linear Pottery culture (LBK), Rössen culture (RSC), Schöningen group (SCG), Baalberge culture (BAC), Salzmünde culture (SMC), Bernburg culture (BEC), Corded Ware culture (CWC), Bell Beaker culture (BBC), Unetice culture (UC), present-day Central European metapopulation (CEM) (N = 500). For further information, see Table S3. The p-values of the clusters are given in percentage of reproduced clusters based on 10,000 bootstrap replicates.
To explore the genetic signal of these population affinities, we have estimated the correlation coefficient between haplogroups and PCA dimensions and performed a significance test (Table 2). K, T2, J, X and also N1a are the haplogroups that clearly influence the separation of the Early/Middle Neolithic cultures from Germany -including also El Mirador- along the first dimension, as opposed to U4 and U5a haplogroups. U and U5b explain the separation of the hunter-gatherers groups along the second dimension.
In none of the analyses El Mirador sample shows close genetic affinities with a contemporaneous Bell Beaker population of 29 specimens gathered from three sites in Germany. The Bell Beaker mtDNA signal is characterized by high frequencies (around 50%) of H haplogroup that in El Mirador only reaches 26%. This heterogeneity in the genetic composition of geographically close populations adds further complexity to future reconstructions of these ancient expansions and correlates with the existence of contemporaneous groups with and without the typical Bell Beaker burial kit.
The generation of complete genomes with the new sequencing technologies will likely contribute to provide a more detailed picture of the complex population movements and affinities along the European prehistory and would eventually explain the dynamics of pan-European Chalcolithic migrations.
mtDNA clone sequences of the El Mirador samples. Samples with potentially conflicting haplotypes or with substitutions that could be attributed to postmortem damage were repeatedly amplified to generate a consensus sequence. Some CRS clones attributable to background contamination have been suppressed for clarity.
Boxplot grouped by geography of El Mirador principal components and other prehistoric cultures. PC1 and PC2 show the differentiation between geographical distributions of ancient cultures. El Mirador population (in yellow) shows affinities with prehistoric Central European cultures despite its location in Spain.
Boxplot grouped by chronology of El Mirador principal components and other prehistoric cultures. PC1 shows the differentiation between hunter-gatherer, Early/Middle Neolithic and Late Neolithic/EBA, whereas PC2 gives information for all the periods. El Mirador population (yellow) have traits of the Early/Middle Neolithic period in these components despite its Chalcolithic attribution.
Details and haplogroup frequencies of El Mirador and present-day populations used in principal component analysis. Relative haplogroup frequencies of El Mirador and previously published populations  were used for principal component analysis. Haplogroups were classified into 23 groups.
Details and haplogroup frequencies of El Mirador and prehistoric cultures used in principal component analysis. Relative haplogroup frequencies of El Mirador and previously published cultures  were used for principal component analysis. Haplogroups were classified into 22 groups.
Details and haplogroup frequencies of El Mirador, Central European metapopulation and prehistoric cultures used in Ward’s hierarchical clustering. Relative haplogroup frequencies of El Mirador and previously published populations  were used for hierarchical Ward clustering. Haplogroups were classified into 20 groups.
Conceived and designed the experiments: CL-F. Performed the experiments: DG-S IO FP LM-L EG M. Lari OR. Analyzed the data: DG-S IO OR SC. Contributed reagents/materials/analysis tools: M. Lari JMV DC. Contributed to the writing of the manuscript: DG-S IO CL-F. Provided archaeological and anthropological information: M. Lozano JMV.
- 1. Whittle AWR (1996) Europe in the Neolithic: The Creation of New Worlds. Cambridge, U.K.: Cambridge University Press.
- 2. Soares P, Achilli A, Semino O, Davies W, Macaulay V, et al. (2010) The Archaeogenetics of Europe. Curr Biol 20: R174–R183.
- 3. Diamond J, Bellwood P (2003) Farmers and their languages: the first expansions. Science 300: 597–603.
- 4. Pinhasi R, Thomas MG, Hofreiter M, Currat M, Burger J (2012) The genetic history of Europeans. Trends Genet 28: 496–505.
- 5. Ammerman AJ, Cavalli-Sforza LL (1984) The Neolithic transition and the Genetics of Population in Europe. Princeton, New Jersey: Princeton University Press.
- 6. Renfrew C, Bahn PG (1991) Archaeology: Theories, methods, and practice. New York, N.Y.: Thames and Hudson.
- 7. Cavalli-Sforza LL, Menozzi P, Piazza A (1994) The history and geography of human genes. Princeton, New Jersey: Princeton University Press.
- 8. Chikhi L, Destro-Bisol G, Bertorelle G, Pascali V, Barbujani G (1998) Clines of nuclear DNA markers suggest a largely neolithic ancestry of the European gene pool. Proc Natl Acad Sci U S A 95: 9053–9058.
- 9. Renfrew C, Boyle K V (2000) Archaeogenetics: DNA and the Population Prehistory of Europe. Cambridge, U.K.: McDonald Institute for Archaeological Research.
- 10. Richards M, Macaulay V, Hickey E, Vega E, Sykes B, et al. (2000) Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet 67: 1251–1276.
- 11. Richards M (2003) The Neolithic Invasion of Europe. Annu Rev Anthropol 32: 135–162.
- 12. Bellwood PS, Renfrew C (2002) Examining the farming/language dispersal hypothesis. Cambridge, U.K.: McDonald Institute for Archaeological Research.
- 13. Haak W, Balanovsky O, Sanchez JJ, Koshel S, Zaporozhchenko V, et al. (2010) Ancient DNA from European Early Neolithic Farmers Reveals Their Near Eastern Affinities. PLoS Biol 8: e1000536.
- 14. Sampietro ML, Lao O, Caramelli D, Lari M, Pou R, et al. (2007) Palaeogenetic evidence supports a dual model of Neolithic spreading into Europe. Proc R Soc B Biol Sci 274: 2161–2167.
- 15. Bramanti B, Thomas MG, Haak W, Unterlaender M, Jores P, et al. (2009) Genetic discontinuity between local hunter-gatherers and central Europe’s first farmers. Science 326: 137–140.
- 16. Malmström H, Gilbert MTP, Thomas MG, Brandström M, Storå J, et al. (2009) Ancient DNA Reveals Lack of Continuity between Neolithic Hunter-Gatherers and Contemporary Scandinavians. Curr Biol 19: 1758–1762.
- 17. Lacan M, Keyser C, Ricaut F-X, Brucato N, Duranthon F, et al. (2011) Ancient DNA reveals male diffusion through the Neolithic Mediterranean route. Proc Natl Acad Sci 108: 9788–9791.
- 18. Gamba C, Fernández E, Tirado M, Deguilloux MF, Pemonge MH, et al. (2012) Ancient DNA from an Early Neolithic Iberian population supports a pioneer colonization by first farmers. Mol Ecol 21: 45–56.
- 19. Deguilloux M-F, Leahy R, Pemonge M-H, Rottier S (2012) European neolithization and ancient DNA: an assessment. Evol Anthropol 21: 24–37.
- 20. Brotherton P, Haak W, Templeton J, Brandt G, Soubrier J, et al. (2013) Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans. Nat Commun 4: 1764.
- 21. Brandt G, Haak W, Adler CJ, Roth C, Szécsényi-Nagy A, et al. (2013) Ancient DNA reveals key stages in the formation of central European mitochondrial genetic diversity. Science 342: 257–261.
- 22. Hervella M, Izagirre N, Alonso S, Fregel R, Alonso A, et al. (2012) Ancient DNA from hunter-gatherer and farmer groups from Northern Spain supports a random dispersion model for the Neolithic expansion into Europe. PLoS One 7: e34417.
- 23. Keller A, Graefen A, Ball M, Matzas M, Boisguerin V, et al. (2012) New insights into the Tyrolean Iceman’s origin and phenotype as inferred by whole-genome sequencing. Nat Commun 3: 698.
- 24. Skoglund P, Malmström H, Raghavan M, Storå J, Hall P, et al. (2012) Origins and genetic legacy of Neolithic farmers and hunter-gatherers in Europe. Science 336: 466–469.
- 25. Skoglund P, Northoff BH, Shunkov M V, Derevianko a P, Paabo S, et al. (2014) Separating endogenous ancient DNA from modern day contamination in a Siberian Neandertal. Proc Natl Acad Sci U S A 111: 2229–2234.
- 26. Sánchez-Quinto F, Schroeder H, Ramirez O, Avila-Arcos MC, Pybus M, et al. (2012) Genomic Affinities of Two 7,000-Year-Old Iberian Hunter-Gatherers. Curr Biol 22: 1494–1499.
- 27. Olalde I, Allentoft ME, Sanchez-Quinto F, Santpere G, Chiang CWK, et al. (2014) Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European. Nature 507: 225–228.
- 28. Vergès J, Allué E, Angelucci D, Cebrià A, Díez C, et al. (2002) La sierra de Atapuerca durante el Holoceno: datos preliminares sobre las ocupaciones de la Edad del Bronce en la Cueva de El Mirador (Ibeas de Juarros, Burgos). Trab Prehist 59: 107–126.
- 29. Cáceres I, Lozano M, Saladié P (2007) Evidence for bronze age cannibalism in El Mirador Cave (Sierra de Atapuerca, Burgos, Spain). Am J Phys Anthropol 133: 899–917.
- 30. Lalueza-Fox C, Rosas A, Estalrrich A, Gigli E, Campos PF, et al. (2011) Genetic evidence for patrilocal mating behavior among Neandertal groups. Proc Natl Acad Sci U S A 108: 250–253.
- 31. Cooper A, Poinar HN (2000) Ancient DNA: Do It Right or Not at All. Science 289: 1139.
- 32. Hofreiter M, Jaenicke V, Serre D, von Haeseler A, Pääbo S (2001) DNA sequences from multiple amplifications reveal artifacts induced by cytosine deamination in ancient DNA. Nucleic Acids Res 29: 4793–4799.
- 33. Pääbo S, Poinar H, Serre D, Jaenicke-Després V, Hebler J, et al. (2004) Genetic analyses from ancient DNA. Annu Rev Genet 38: 645–679.
- 34. Suzuki R, Shimodaira H (2006) Pvclust: an R package for assessing the uncertainty in hierarchical clustering. Bioinformatics 22: 1540–1542.
- 35. Meyer M, Fu Q, Aximu-Petri A, Glocke I, Nickel B, et al. (2013) A mitochondrial genome sequence of a hominin from Sima de los Huesos. Nature 505: 403–406.
- 36. Patterson N, Moorjani P, Luo Y, Mallick S, Rohland N, et al. (2012) Ancient Admixture in Human History. Genetics 192: 1065–1093.
- 37. Czebreszuk J (2003) Bell beakers from west to east, Vol. 8000. In: Bogucki PI, Crabtree PJ, editors. Ancient Europe 8000 B.C. - A.D 1000: An encyclopedia of the barbarian world, Vol. 2. Charles Scribner’s Sons, New York. 476–485.