The Vikings (or Norse) played a prominent role in Irish history but, despite this, their genetic legacy in Ireland, which may provide insights into the nature and scale of their immigration, is largely unexplored. Irish surnames, some of which are thought to have Norse roots, are paternally inherited in a similar manner to Y-chromosomes. The correspondence of Scandinavian patrilineal ancestry in a cohort of Irish men bearing surnames of putative Norse origin was examined using both slow mutating unique event polymorphisms and relatively rapidly changing short tandem repeat Y-chromosome markers. Irish and Scandinavian admixture proportions were explored for both systems using six different admixture estimators, allowing a parallel investigation of the impact of method and marker type in Y-chromosome admixture analysis. Admixture proportion estimates in the putative Norse surname group were highly consistent and detected little trace of Scandinavian ancestry. In addition, there is scant evidence of Scandinavian Y-chromosome introgression in a general Irish population sample. Although conclusions are largely dependent on the accurate identification of Norse surnames, the findings are consistent with a relatively small number of Norse settlers (and descendents) migrating to Ireland during the Viking period (ca. AD 800–1200) suggesting that Norse colonial settlements might have been largely composed of indigenous Irish. This observation adds to previous genetic studies that point to a flexible Viking settlement approach across North Atlantic Europe.
The Vikings or Norse have played a prominent role in Irish history. After first recorded contact in AD 795 they are credited with establishing Ireland's first true urban settlements including modern Dublin, Limerick and Cork.1, 2 It is generally agreed that present day Norway was the source of Ireland's Viking raiders and settlers but despite their apparent historical prominence, other lines of evidence, including the scarcity of Norse place names in Ireland and the paucity of word borrowing from Norse into Irish, argue against any large-scale Viking immigration.3 In addition, there also appears to have been extensive integration between the Irish and Norse leading to a fusion ‘Hiberno–Norse’ material culture in areas of Viking settlement. Nonetheless, the inhabitants of Hiberno–Norse towns were distinctively referred to as Ostmen (old Norse for ‘men of the east’) to distinguish them from the rest of Ireland.4
The genetic legacy of the Viking age is well characterised for many areas of North Atlantic Europe.5, 6, 7, 8 However, there has been relatively little investigation of their impact on the Irish gene pool. Principal component analysis (PCA) of Y-chromosome allele (haplogroup) frequencies suggested little or no Norse introgression in Ireland, whereas maximum likelihood admixture calculations indicated a substantial 34.8% Norwegian ancestry in a Dublin hinterland sample.9 However, the confidence intervals on this estimate encompassed virtually zero to total Norwegian ancestry.
Unlike many areas of the British Isles, Norse kingdoms in Ireland were limited in contiguous geographic extent1 and centred on now highly urbanised cities making it difficult to reliably identify modern potential Norse-Irish geographic populations. As an alternative approach, we used the patrilineal coinheritance of surnames and Y-chromosomes.10 Surnames were first adopted in Ireland from ca. AD 900 to 1200, roughly coinciding with the period of Viking activity. During this time, numerous Norse personal names (and nicknames) were introduced onto the island, which later passed into hereditary surnames often by the prefixing of Mac or Ó, meaning ‘son of’ and ‘grandson/descendent of’, respectively. Not every putative Norse surname must necessarily have been founded by a Norse male. However, as a group, current bearers of these surnames have a prima facie link to Viking society and may be at least enriched for such ancestry. A previous Irish Y-chromosome11 study using this approach successfully identified a distinctive paternal population history for Irish groups with surnames of exogenous (English and Scottish) origin. A group of Norman and Norse surnames showed less evidence for an unusual, Y-chromosome history though the sample size was small.
We have assembled a cohort 47 Irish men bearing surnames of putative Norse origin and characterised the Y-chromosome diversity of each through unique event polymorphism (UEP) and short tandem repeat (STR) loci. The relative proportions of Irish and Scandinavian ancestry are examined independently for UEP and STR diversity, using six different admixture estimators to examine the scale and nature of Norse settlement in Ireland and allow a parallel investigation of the impact of method and marker choice on Y-chromosome admixture estimates.
Materials and methods
Samples and genotyping
Norse surnames were identified according to McLysaght,12 the major general reference for individual Irish surname origins. The number of surnames with a putative Norse origin is relatively low and in some cases there are multiple possible origins for a single surname. For these reasons, the sample population of 47 men came from 26 names thus including multiple representatives of some names as follows (number): Arthur (2), Beirne (2), Bligh (1), Boland (3), Caskey (1), Coll (1), Coppinger (2), Doyle (4), Gohery (2), Hanrick (2), Harold (1), Hendrick (1), Higgins (2), Kells (2), Kettle (1), Loughlin (1), McGetrick (3), McLoughlin (3), Nelson (1), Norris (1), O’Higgins (1), Sugrue (2), Sweetnam (1), Thunder (1), Toner (3) and Tormey (3). Volunteers were recruited through personal contacts or postal request to relevant surname bearers selected from telephone directories. Most of these came from geographic areas associated with Norse activity in Ireland.
DNA was extracted using a standard phenol/chloroform protocol and each sample genotyped for 13 STR loci (DYS19, DYS388, DYS390, DYS391, DYS392, DYS393, DYS385A, DYS385B, DYS389I, DYS389II, DYS460, DYS461, and DYS462) in two multiplexes (MS1 and EBF) essentially as previously described.13 Up to six UEPs (M269, M170, M26, SRY-1532.2 (SRY10831.2), M35, YAP), which divide samples into broader haplogroups,14, 15 were also examined in a hierarchical manner using polymerase chain reaction/restriction fragment length polymorphism assays. Although STR profiles were generated for 47 samples, complete UEP typing was only possible for 43 of these. The haplogroups of the remaining four samples were inferred from their STR profiles by comparison to a database of ∼2000 Irish Y-chromosomes16, 17 typed for these STRs and UEPs.
The current data were analysed primarily in concert with published Y-chromosome data for Ireland, Scandinavia and Britain.9 Norse surname group (NSG) Y-chromosomes were divided into haplogroups as outlined by Capelli et al.9 The single nucleotide polymorphisms M173 and M17 used in the former study were not typed in the NSG. However, M269 and SRY1532.2, respectively, were taken as phylogenetic equivalents for the purposes of comparable haplogroup definition. Virtually all North-West Europe haplogroup R Y-chromosomes appear to either have the derived allele for SRY1532.2 and M17 or M173 and M269 meaning that this treatment introduces minimal error (the full Y-chromosome phylogenetic tree can be seen in Jobling and Tyler-Smith15). STR-based analysis was restricted to six marker haplotypes (DYS19, DYS388, DYS390, DYS391, DYS392 and DYS393) to allow maximum comparability between datasets.
Under the hypothesis that the NSG is an admixed Irish-Norse population, we attempted to estimate the admixture proportion (m) derived from each parental population. These estimates are generally based on allele frequencies in modern parental and hybrid populations. However, these can fluctuate after the admixture event by genetic drift, migration, mutation or selection. Sample population allele frequencies may also suffer from stochastic sampling error. Several different admixture estimation methodologies are commonly used, many of which try to incorporate some of these potential complications.18 However, no current admixture method can fully account for all of them. Six of the most commonly employed estimators were used to provide a broad-based assessment of NSG admixture proportions.
Estimates were carried out using UEP and STR diversity independently because of difficulties in combining both for some methods (see Helgason et al6). This dual approach allows an investigation of the efficacy of methods based on a small number of discrete alleles (haplogroups) versus those from a higher number of alleles (multi-STR loci haplotypes), which have a greater ‘noise’ risk from recurrent and back mutations. UEP alleles are simply represented by the 11 haplogroups defined in Capelli et al9 whereas Y-chromosome STR alleles are compound haplotypes of six STR loci. The first parental population (P1) was an Irish sample (n=119), whereas a Norwegian sample (n=201) represented the second parental population (P2).9 This data set was chosen to allow strict comparability in sample populations between UEP and STR-based admixtures estimates. A brief description of each admixture estimator examined follows:
mR19: A least-squares estimator that directly uses allele frequencies in calculations. mR was estimated using ADMIX 2.0.20, 21 Confidence intervals are given by the standard deviation over 10 000 random bootstrap samples.
mC:22, 23 A later variation on mR, mC atempts to incorporate the effects of drift in the hybrid population and stochastic sampling error in the hybrid and parental populations. mC was calculated using LEADMIX24 (‘Likelihood Estimation of Admixture’), Version 2.0 (http://zoo.cam.ac.uk/ioz/software.html).
mY20: incorporates the effect of mutation since the admixture event. The molecular relationship between alleles was defined as the number of pairwise differences for UEP haplogroups or the sum of the squared difference in allele sizes for STR haplotypes. The date of the admixture event was set at 1000 years ago applying a mutation rate of 2.2 × 10−7 per year for UEPs25 and 1.38 × 10−5 per year for six-locus STR haplotypes.26 (The use of alternative rates was not found to significantly affect the results in this case.) Computations were carried out using ADMIX 2.0.20, 21 Confidence intervals were obtained as the standard deviation of 10 000 random bootstrap samples.
mL27: A coalescent-based maximum likelihood method. Ancestral allele frequencies compatible with the observed data are reconstructed and the probabilities of obtaining the current frequencies in the hybrid group are calculated for different parental population contributions. mL was calculated using LEA27 (‘Likelihood-based Estimation of Admixture’) (http://www.rubic.rdg.ac.uk/~mab/software.html) with 55 000 Markov chain Monte Carlo (MCMC) iterations, the first 5000 discarded as burn-in. The median value was taken as the estimate of mL whereas the 97.5 and 2.5 percentiles provided the 95% credible interval.
mW:24 A maximum likelihood approach that emphasises the effect of genetic drift, both in terms of parental population differentiation prior to the admxiture event and subsequently in the admixed and parental populations. It also incorporates the effect of sampling error for each population. mW estimates were calculated using LEADMIX24 and are returned bounded by 95% credible intervals.
mρ:6 mρ allows for the incorporation of ‘private lineages’ (alleles not observed/sampled in either parental population possibly owing to mutation since the admixture event) by identifying the closest match (or matches) as an ancestral haplotype(s). Distances between alleles, for the identification of potential ancestor(s) of private lineages, were defined as the sum of repeat unit difference between haplotypes. Computations were implemented using software6 provided by Agnar Helgason (deCODE Genetics, Reykjavík).
The relationship of the NSG to 10 geographically defined population groupings in the North Atlantic region was also examined using a genetic distance approach. Norwegian (n=201) and Danish/North German (n=190) population samples were taken directly from Capelli et al9 while a number of British Isles subpopulations were generated from the same data by combining smaller groupings as follows (n): Ireland (119); Scottish Isles (272); Scotland (178); Wales (196); England North (231); England Midlands (205); England Southwest (125); England Southeast (256).
Once again analysis was conducted independently for UEP and STR markers using the ARLEQUIN package28 (Version 2.000). Population genetic distances, as linearised ΦST values, were calculated from the mean pairwise difference between UEP haplotypes. ΦST significance was ascertained by randomly permuting individuals across populations over 10 000 replicate analyses. The interpopulation ΦST matrix was summarised in two-dimensional space using the ALSCAL program in the SPSS package (Version 11.0, SPSS Inc.). A similar analysis was conducted for six-STR loci haplotypes using linearised RST values.
There is a generally strong correlation of Irish surnames with Y-chromosomes indicating shared recent patrilineal ancestry.17 However, this varies considerably between names, reflecting different origins (single versus multiple founders) and the impact of post-foundation male introgression. Thirty-four (13 STR) haplotypes were observed in our cohort of 47 men bearing one of 26 putative Norse surnames. Most haplotypes are either unique or found across different surnames (Genotype data can be found in Supplementary Table 1). However, there is some Y-chromosome haplotype sharing within surnames; for example, in the Arthur, Hanrick and Gohery surnames both samples from each were identical suggesting a single origin or introduction to Ireland. Conversely, all four Doyle Y-chromosomes are different to each other tentatively pointing to multiple foundations.
Previous studies have identified Y-chromosome lineages that are thought to be indicative of Viking contact and introgression. Two such UEP/STR-defined haplotypes and their one-step STR neighbours (‘+1’ those haplotypes differing by one STR repeat over all loci) are found at high frequency in Norway (representing the Viking source population) and other areas affected by Viking migrations.29 These types, termed 2.47+1 and 3.65+1, are either absent or at low frequency in the NSG (Figure 1). In contrast, the Atlantic modal haplotype (AMH+1) within haplogroup R1 × R1a (R1b3), typical of Ireland and Western Britain, is very common in the NSG. The N3 and P × R1 haplogroups also found in Norway at appreciable frequencies are absent in the British Isles (other than the Orkney Islands)9 and the NSG. Overall, of the 20 STR haplotypes found in the NSG (based on a truncated 6 STR haplotype for inter-data set comparison) only one is more common in Norway than Ireland, 12 display the converse pattern, whereas seven are unique to the NSG (Supplementary Table 2).
We also examined the occurrence of these putative Viking marker lineages in a general Irish population sample of 796 Y-chromosomes.16 However, these are not frequent (<0.5%) in the Irish population as a whole nor do they comprise a large fraction of Y-chromosomes in any of nine smaller geographic Irish subgroupings, indicating no strong regional-specific introgression.
The relationship of the NSG group to 10 North Atlantic European geographic populations was further examined, for UEP and STR diversity separately, using genetic distances (ΦST and RST respectively). Multidimensional scaling (MDS) summaries of these pairwise genetic distance markers are shown in Figure 2. Each of the two dimensions are strongly correlated between the different marker systems (r=∼0.9) and demonstrate a significant differentiation of Norwegian and Irish Y-chromosomes and a markedly closer affinity of the NSG to Ireland. This is particularly evident within relationships based on multi-STR haplotypes, which seem to have a generally greater discriminatory power. For example, they reveal a degree of distinction between Ireland and Scotland/Wales, despite their close linkage in UEP-based analyses owing to their shared high frequency of the R1b3 haplogroup.
We next attempted to formally quantify Irish and Norwegian ancestry proportions in the NSG using six different admixture estimators, each of which considers different factors and complexities in its execution. The results of this survey are shown in Figure 3. There is good correlation between most estimators with virtually all, whether using UEP or STR markers, supporting a substantial majority contribution from Ireland to the NSG.
The unconstrained estimators (mR, mC and mY) often returned notional Irish ancestry proportions greater than 1. Interpreting these as a 100% Irish contribution, the average estimate is ∼90% Irish admixture with a standard deviation (SD) across estimates of 15.4%. The maximum likelihood mL estimate based on UEP variation is exceptional in suggesting a minority (49%) Irish ancestry in the NSG. If this outlier is excluded the average estimate increases to ∼95% and the SD more than halves to 7.3%. mL calculation based on more numerous STR-defined alleles (haplotypes) returns an estimate of 93% Irish ancestry in agreement with other methods.
In some instances, a median value of mL (reported in Figure 3) can give a poor representation of the results over the entire MCMC run.27 The complete distribution of Irish ancestry estimates over the run of 50 000 MCMC iterations is shown in Figure 4. Analysis based on UEP-defined alleles (11 haplogroups) did not converge toward a consistent estimate whereas corresponding STR-defined alleles (106 haplotypes) show an unambiguous tendency toward a high Irish ancestry proportion estimate. Substantially longer chains (up to 250 000 MCMC iterations) were not found to aid UEP estimate convergence. It appears that the majority Norwegian ancestry mL estimate is an artefact of poor LEA convergence.
We also conducted additional admixture analysis with these methods using independent parental populations data sets including a larger Irish grouping (n=221)11 and separate Norwegian (n=250),6, 30, 31 Danish (n=69)6, 32 or Swedish (n=110)30 populations. To allow comparability between data sets, this analysis was based on five STR haplotypes (DYS19, DYS390, DYS391, DYS392 and DYS393). However, all estimates, whatever the Scandinavian parental population, returned a ∼90% Irish contribution or greater. Consequently, there is no evidence of major Scandinavian ancestry in the NSG from any of our analyses.
There is little convincing evidence for substantial Scandinavian patrilineal ancestry in a cohort of Irish men bearing surnames of putative Norse origin. The absence of an appreciable legacy in both the general Irish population sample and this subgroup with a potential historical/cultural link to Norse society suggests a very limited general Norse genetic legacy in Ireland dating to the Viking period (ca. AD 800–1200). Substantial Irish ancestry in the NSG is not unexpected given historical evidence of assimilation between the native Irish and Norse settlers. However, the Norse genetic component of the distinctive hybrid Hiberno–Norse culture appears absent. It may be that the number of Norse and their descendents who settled and remained in Irish Norse colonies was small compared to their overall population; perhaps restricted to a thin, upper, stratum of these societies. The bulk of the Hiberno–Norse settlement population over the longer term may simply have been culturally adapted indigenous Irish.
Although the use of surname information to investigate historical questions is potentially powerful11, 16, 17 any inference inherently relies on the accurate assessment of surname origin. The perturbed nature of Irish surname history means that similar or identical names can have more than one source.12, 17, 33 For example, the name Sweetman can be of Norse origin or English toponymic from Swettenham.12 The presence of several haplotypes within the NSG not found in the Irish or Norwegian samples may hint at this possibility. For example, there are multiple instances of the E3b haplogroup that is more typical of England than either Ireland or Scandinavia.9 Alternatively, unique haplotypes, might indicate the action of drift over time. This could distort current allele frequencies and consequently population relationships and admixture estimates.
The proposed model of Viking migration is based not only on a Norse root for the surnames examined but also requires that the personal names from whence these derived were largely restricted to Hiberno–Norse settlements. There is some evidence that they had a degree of popularity in a native Irish context34 and if such exchange was common it may mean that Norse names had begun to become disassociated with Norse colonial societies by the time of widespread surname adoption. The original personal names/nicknames could also have been introduced through a Norse female or indeed any other nonpatrilineal ancestor leaving no Y-chromosome trace when these names eventually became incorporated into hereditary surnames.
Finally, there is also an expected rate of disassociation of surname from initial ancestry owing to nonpaternity, adoptions and other causes. We have previously estimated this rate at 1.6% per generation,17 which would be expected to roughly halve any initial Scandinavian ancestry fraction over ∼1000 years (∼40 generations). The presence of multiple haplotypes within some surnames may be indicative of this, although it may also represent multiple surname foundations/origins.
The foregoing possibilities are not mutually exclusive and all may contribute to the overwhelming Irish ancestry observed in the putative NSG. Under a ‘worst-case’ scenario, where all putative Norse surnames have an alternate origin, the results apply to a general albeit small Irish population sample and still indicate very little Norse migration to Ireland. However, the use of a variety of names and the inclusion of multiple bearers should help to cushion the impact of potential confounding factors (eg, some names not having a true Norse origin or the effect of subsequent nonpaternity events), allowing the identification of a grouping that is, at least, substantially enriched for Norse patrilineal ancestry.
Although open to interpretation, the limited Scandinavian admixture is a consistent and robust finding across several different admixture estimators, which encompass a range of considerations and computational frameworks. The choice of the most appropriate single estimator will depend on the expected relative importance of potential confounding factors. For example with recent admixture or UEP data, the effect of mutation is of less importance than drift. Despite the potential limitations of a relatively small number of alleles when using UEP haplogroups or the ‘noise’ from recurrent/back mutation associated with highly variable multi-STR haplotypes, both marker types generally return consistent and sensible results. UEP diversity is often favoured in population comparisons because of stability and obvious structure. However, STRs have potentially wider application in measuring diversity and finer-scale intra-haplogroup relationships. The use of a small number of STRs with moderate mutation rates that can be conveniently typed in a single multiplex may represent an under- utilised tool in macro-Y-chromosome population genetics.
The mL maximum likelihood method27 based on UEP Y-chromosome variation was a notable exception in our analysis as a median estimate indicated majority Scandinavian ancestry in the NSG. Although it performed well in STR-based analysis, where a large number of alleles are used, it appears that the method is considerably less accurate when the number of alleles is small. This observation may explain, in part at least, previous mL Y-chromosome admixture estimates indicating high (35%) Scandinavian ancestry in a Dublin hinterland sample.9 It may also be a relevant consideration in resolving the widely discrepant estimates of modern European ancestry attributed to the Neolithic or Palaeolithic periods using the same Y-chromosome data but different approaches, including mL.35, 36
Although the conclusions are predicated on the assumption that our cohort of Norse surnames largely originated in Hiberno–Norse society, they are consistent with limited Norse migration to Ireland. This observation may fit into a broader emerging picture, revealed by Y-chromosome and mitochondrial DNA, of Viking flexibility and adaptability in their settlement patterns across the North Atlantic. These included roughly equal male and female contributions through family-based migration, to secure settlements near Scandinavia and the integration of Gaelic females on frontier settlements further west, predominantly founded by Norse males.8 In Ireland successful settlement may have involved the wholesale incorporation of the indigenous Irish to create a distinctive, fusion Hiberno–Norse colonial society.
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This work was funded in part by a Health Research Board of Ireland grant (RP/2004/155) and Patrick Guinness and Joseph A Donohoe through the Trinity Trust. We are grateful to the volunteers who donated DNA samples together with Luzveminda O’Sullivan and Nessa O’Sullivan who facilitated their collection. We also thank Lounès Chikhi and Martin O’Hely (Université Paul Sabatier, Toulouse), who compiled a new version of LEA to allow more than 100 alleles at each locus, Agnar Helgason, who kindly provided the software for mρ calculations and Caitriona Murray for helpful comments on the manuscript.
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McEvoy, B., Brady, C., Moore, L. et al. The scale and nature of Viking settlement in Ireland from Y-chromosome admixture analysis. Eur J Hum Genet 14, 1288–1294 (2006). https://doi.org/10.1038/sj.ejhg.5201709
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