Iberia: East Bell Beakers spread Indo-European languages; Celts expanded later


New paper (behind paywall), The genomic history of the Iberian Peninsula over the past 8000 years, by Olalde et al. Science (2019).

NOTE. Access to article from Reich Lab: main paper and supplementary materials.


We assembled genome-wide data from 271 ancient Iberians, of whom 176 are from the largely unsampled period after 2000 BCE, thereby providing a high-resolution time transect of the Iberian Peninsula. We document high genetic substructure between northwestern and southeastern hunter-gatherers before the spread of farming. We reveal sporadic contacts between Iberia and North Africa by ~2500 BCE and, by ~2000 BCE, the replacement of 40% of Iberia’s ancestry and nearly 100% of its Y-chromosomes by people with Steppe ancestry. We show that, in the Iron Age, Steppe ancestry had spread not only into Indo-European–speaking regions but also into non-Indo-European–speaking ones, and we reveal that present-day Basques are best described as a typical Iron Age population without the admixture events that later affected the rest of Iberia. Additionally, we document how, beginning at least in the Roman period, the ancestry of the peninsula was transformed by gene flow from North Africa and the eastern Mediterranean.

Interesting excerpts:

From the Bronze Age (~2200–900 BCE), we increase the available dataset (6, 7, 17) from 7 to 60 individuals and show how ancestry from the Pontic-Caspian steppe (Steppe ancestry) appeared throughout Iberia in this period (Fig. 1, C and D), albeit with less impact in the south (table S13). The earliest evidence is in 14 individuals dated to ~2500–2000 BCE who coexisted with local people without Steppe ancestry (Fig. 2B). These groups lived in close proximity and admixed to form the Bronze Age population after 2000 BCE with ~40% ancestry from incoming groups (Fig. 2B and fig. S6).

Y-chromosome turnover was even more pronounced (Fig. 2B), as the lineages common in Copper Age Iberia (I2, G2, and H) were almost completely replaced by one lineage, R1b-M269. These patterns point to a higher contribution of incoming males than females, also supported by a lower proportion of nonlocal ancestry on the X-chromosome (table S14 and fig. S7), a paradigm that can be exemplified by a Bronze Age tomb from Castillejo del Bonete containing a male with Steppe ancestry and a female with ancestry similar to Copper Age Iberians.


For the Iron Age, we document a consistent trend of increased ancestry related to Northern and Central European populations with respect to the preceding Bronze Age (Figs. 1, C and D, and 2B). The increase was 10 to 19% (95% confidence intervals given here and in the percentages that follow) in 15 individuals along the Mediterranean coast where non-Indo-European Iberian languages were spoken; 11 to 31% in two individuals at the Tartessian site of La Angorrilla in the southwest with uncertain language attribution; and 28 to 43% in three individuals at La Hoya in the north where Indo-European Celtiberian languages were likely spoken (fig. S6 and tables S11 and S12).

This trend documents gene flow into Iberia during the Late Bronze Age or Early Iron Age, possibly associated with the introduction of the Urnfield tradition (18). Unlike in Central or Northern Europe, where Steppe ancestry likely marked the introduction of Indo-European languages (12), our results indicate that, in Iberia, increases in Steppe ancestry were not always accompanied by switches to Indo-European languages.

I think it is obvious they are extrapolating the traditional (not that well-known) linguistic picture of Iberia during the Iron Age, believing in continuity of that picture (especially non-Indo-European languages) during the Urnfield period and earlier.

What this data shows is, as expected, the arrival of Celtic languages in Iberia after Bell Beakers and, by extension, in the rest of western Europe. Somewhat surprisingly, this may have happened during the Urnfield period, and not during the La Tène period.

Also important are the precise subclades:

We thus detect three Bronze Age males who belonged to DF27 (154, 155), confirming its presence in Bronze Age Iberia. The other Iberian Bronze Age males could belong to DF27 as well, but the extremely low recovery rate of this SNP in our dataset prevented us to study its true distribution. All the Iberian Bronze Age males with overlapping sequences at R1b-L21 were negative for this mutation. Therefore, we can rule out Britain as a plausible proximate origin since contemporaneous British males are derived for the L21 subtype.

New open access paper Survival of Late Pleistocene Hunter-Gatherer Ancestry in the Iberian Peninsula, by Villalba-Mouco et al. Cell (2019):

BAL0051 could be assigned to haplogroup I1, while BAL003 carries the C1a1a haplogroup. To the limits of our typing resolution, EN/MN individuals CHA001, CHA003, ELT002 and ELT006 share haplogroup I2a1b, which was also reported for Loschbour [73] and Motala HG [13], and other LN and Chalcolithic individuals from Iberia [7, 9], as well as Neolithic Scotland, France, England [9], and Lithuania [14]. Both C1 and I1/ I2 are considered typical European HG lineages prior to the arrival of farming. Interestingly, CHA002 was assigned to haplogroup R1b-M343, which together with an EN individual from Cova de Els Trocs (R1b1a) confirms the presence of R1b in Western Europe prior to the expansion of steppe pastoralists that established a related male lineage in Bronze Age Europe [3, 6, 9, 13, 19]. The geographical vicinity and contemporaneity of these two sites led us to run genomic kinship analysis in order to rule out any first or second degree of relatedness. Early Neolithic individual FUC003 carries the Y haplogroup G2a2a1, commonly found in other EN males from Neolithic Anatolia [13], Starçevo, LBK Hungary [18], Impressa from Croatia and Serbia Neolithic [19] and Czech Neolithic [9], but also in MN Croatia [19] and Chalcolithic Iberia [9].

See also

Minimal Corded Ware culture impact in Scandinavia – Bell Beakers the unifying maritime elite


Chapter The Sea and Bronze Age Transformations, by Christopher Prescott, Anette Sand-Eriksen, and Knut Ivar Austvoll, In: Water and Power in Past Societies (2018), Emily Holt, Proceedings of the IEMA Postdoctoral Visiting Scholar Conference on Theories and Methods in Archaeology, Vol. 6.

NOTE. You can download the chapter draft at Academia.edu.

Abstract (emphasis mine):

Along the western Norwegian coast, in the northwestern region of the Nordic Late Neolithic and Bronze Age (2350–500 BCE) there is cultural homogeneity but variable expressions of political hierarchy. Although new ideological institutions, technology (e.g., metallurgy and boat building), intensified agro‑pastoral farming, and maritime travel were introduced throughout the region as of 2350 BCE, concentrations of expressions of Bronze Age elites are intermittently found along the coast. Four regions—Lista, Jæren, Karmøy, and Sunnmøre—are examined in an exploration of the establishment and early role of maritime practices in this Nordic region. It is argued that the expressions of power and material wealth concentrated in these four regions is based on the control of bottlenecks, channels, portages, and harbors along important maritime routes of travel. As such, this article is a study of prehistoric travel, sources of power, and maritime landscapes in the Late Neolithic and Early Bronze Age of Norway.

Interesting excerpts:

(…)The [Corded Ware culture (CWC)] in Norway (or Battle Axe Culture, 2750–2400/2350 BCE) is primarily represented in Eastern Norway, with a patchy settlement pattern along the Oslo fjord’s coast through the inland valleys to Trøndelag in Central Norway (Hinsch 1956). The CWC represents an enigmatic period in Norwegian prehistory (Hinsch 1956; Østmo 1988:227–231; Prescott and Walderhaug 1995; Shetelig 1936); however the data at the moment suggests the following patterns:

  • Migration: The CWC was the result of a small‑scale immigration, but did not trigger substantial change.
  • Eastern and limited impact: The CWC was primarily located in small settlement patches in eastern Norway.
  • Terrestrial: In terms of maritime practices, the CWC does not represent a significant break from older traditions, though it seems to have a more pronounced terrestrial bearing. It is conceivable that pastures and hunting grounds were a more important political‑economic resource than waterways.

The mid‑third millennium in Norway, around 2400 BCE, represents a significant reorientation. Bell Beaker Culture (BBC) settlements in western Denmark and Norway archaeologically mark the instigation of the Nordic LN, though much of the historical process leading from the Bell Beaker to the Late Neolithic, 2500 to 2350 BCE, remains unclear (Prescott 2012; Prescott and Melheim 2009; Prieto‑Martinez 2008:116; Sarauw 2007:66; Vandkilde 2001, 2005). Still, the outcome is the establishment of the Nordic region of interaction in the Baltic, Northern Germany, Sweden, Denmark, and Norway. The distribution of artifact materials such as Bell Beakers and flint daggers attests to the far‑flung network of regular exchange and communication. This general region of interaction was reproduced through the Late Neolithic and Bronze Age.

The Nordic region in the Late Neolithic and Bronze Age. Sites and regions discussed in the text are marked (ater Prescott and Glørstad 2015:fig. 1).

The transition from the preceding Neolithic period hunter‑gatherer societies was rapid and represents a dramatic termination of hunter‑gatherer traditions. It has been argued that the transformation is tied to initial migrations of people to the western coast of Norway from BBC areas, possibly from northern Jutland (Prescott 2011; Prescott and Walderhaug 1995:273). Bifacial tanged‑and‑barbed points, often referred to as “Bell Beaker points,” probably represent an early, short phase of the BBC‑transition around 2400 BCE. In Norway these points have a predominantly western and coastal distribution (Østmo 2012:64), underscoring the maritime nature of the initial BBC‑expansion.

Distribution routes for LN1 flint daggers type 1 suggesting communication routes and networks. (Redrawn after fig. 9, Apel 2001:17).

(…) In response to the question about what attracted people from Bell Beaker groups to western Norway, responses have hypothesized hunting products, political power, pastures, and metals. Particularly the latter has been emphasized by Lene Melheim (2012, 2015:37ff).

A recent study by Melheim and Prescott (2016) integrated maritime exploration with metal prospecting to explain initial excursions of BBC‑people along the western coast and into the fjords. Building on the archaeological concept of traveling metal prospectors as an element in the expansion of the Bell Beaker phenomenon, in combination with anthropological perspectives on prospecting, the article explores how prospecting for metal would have adjusted to the landscapes of western Scandinavia. Generally speaking, prospecting seldom leads to successful metal production, and it is difficult to study archaeologically. However, it will often create links between the prospectors’ society and indigenous groups, opening new territories, and have a significant transformative impact—on both the external and indigenous actors and societies.

While the text echoes the traditional idea that Corded Ware spread Indo-European languages, Prescott (since Prescott and Walderhaug 1995) is a supporter of the formation of a Nordic community and a Nordic (i.e. Pre-Germanic) language with the arrival of Bell Beakers.

An identification of the Corded Ware language as of a previous Proto-Indo-European stage is possible, as I have previously said (although my preference is Uralic-related languages).

This CWC language would thus still form the common substrate to both Germanic and Balto-Slavic, both being North-West Indo-European dialects, which spread with Bell Beakers over previous Corded Ware territory.

NOTE. This pre-LPIE nature could be in turn related to Kortlandt’s controversial proposal of an ealier PIE dative *-mus shared by both branches. However, that would paradoxically be against Kortlandt’s own assumption that the substrate was in fact of a non-Indo-European nature

See also:

Yleaf: software for human Y-chromosomal haplogroup inference from next generation sequencing data


Brief communication (behind paywall) Yleaf: software for human Y-chromosomal haplogroup inference from next generation sequencing data, by Arwin Ralf, Diego Montiel González, Kaiyin Zhong, and Manfred Kayser, Mol Biol Evol (2018), msy032.


Next generation sequencing (NGS) technologies offer immense possibilities given the large genomic data they simultaneously deliver. The human Y chromosome serves as good example how NGS benefits various applications in evolution, anthropology, genealogy and forensics. Prior to NGS, the Y-chromosome phylogenetic tree consisted of a few hundred branches, based on NGS data it now contains many thousands. The complexity of both, Y tree and NGS data provide challenges for haplogroup assignment. For effective analysis and interpretation of Y-chromosome NGS data, we present Yleaf, a publically available, automated, user-friendly software for high-resolution Y-chromosome haplogroup inference independently of library and sequencing methods.

Here is a link to the software Yleaf’s website, from the Department of Genetic Identification, at the University of Erasmus Medical Center.

Summary of NGS datasets used for automated NRY haplogrouping with Yleaf


In the time of NGS (or massively parallel sequencing, MPS), the amount of genomic data produced and made publically available is rapidly expanding, providing valuable resources for many areas of research and applications. Due to its haploid nature and male-specific inheritance, the non-recombining part of the human Y-chromosome (NRY) is highly suitable for phylogenetic studies and for addressing questions in evolution, anthropology, population history, genealogy and forensics (Jobling & Tyler-Smith, 2017). Over recent years, NGS data allowed the phylogenetic NRY tree to dramatically increase in size and complexity (Hallast et al. 2014; Poznik et al. 2016). The two most comprehensive tree versions ISOGG (http://www.isogg.org/tree) and Yfull (https://www.yfull.com/tree) currently contain thousands of branches. However, the complexity of both, Y tree and NGS data provide immense challenges for NRY haplogroup assignment, which reflects a key element in many NRY applications. Here we introduce Yleaf, a Phyton-based, easy-to-use, publically-available software tool for effective NRY single nucleotide polymorphism (SNP) calling and subsequent NRY haplogroup inference from NGS data. By comparative whole genome data analysis, we demonstrate high concordance of Yleaf in NRY-SNP calling compared to well-established tools such as SAMtools/BCFtools (Li et al. 2009), and GATK (McKenna, et al. 2010) as well as improved performance of Yleaf in NRY haplogroup assignment relative to previously developed tools such as clean_tree (Ralf et al. 2015), AMY-tree (Van Geystelen et al. 2015), and yHaplo (Poznik, 2016).

Yleaf allows analyzing NRY sequence data from many types of NGS libraries i.e., whole genomes, whole exomes, large genomic regions, and large numbers of targeted amplicons. Several modifications relative to our previously developed clean_tree tool (Ralf et al. 2015) were implemented to optimize the performance especially relevant for extremely large NGS datasets such as whole genomes. For instance, Yleaf extracts the Y-chromosomal reads prior to further processing and uses multi-threading, a batch option is included too. Importantly, Yleaf provides drastically increased haplogroup resolution i.e., from Downloaded from 530 positions defining 432 NRY haplogroups with clean_tree (Ralf et al. 2015) to over 41,000 positions defining 5353 haplogroups with Yleaf. For a detailed method description see the supplementary material.

Featured image: From Martiniano et al. (2017).