Paths and timings of the peopling of Polynesia inferred from genomic networks
Open accessAbstract
Genome-wide study reconstructing a serial founder expansion through Polynesia with Hawaiian settlement situated within the East Polynesian migration sequence.
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Claims the paper makes
30 of 77 cited sources checked · 6 supported · 2 flagged · accuracy not yet measured
- Findingown data
The genome-wide network dates support the radiocarbon-based short chronology of Wilmshurst et al. as corrected by Mulrooney et al., rather than the long or intermediate chronologies.
“The dates that we infer from our genome-wide network analyses support the radiocarbon-based ‘short chronology’ from the comprehensive re-analysis of Wilmshurst et al.12 as corrected by Mulrooney et al.3 (Extended Data Table 1), as opposed to the prior nearly one thousand year older ‘long chronology’2,4, and as opposed to the intermediate chronology suggested by Spriggs and Anderson13”
Quote in the paperSubstantial claim1 of 4 sources checked- cites [12] Wilmshurst, J. M., Hunt, T. L., Lipo, C. P. & Anderson, A. J. High-precision radiocarbon dating shows recent and rapid initial human colonization of East Polynesia. Proc. Natl Acad. Sci. USA 108, 1815–1820 (2011). source
- cites [3] Mulrooney, M. A., Bickler, S. H., Allen, M. S. & Ladefoged, T. N. High-precision dating of colonization and settlement in East Polynesia. Proc. Natl Acad. Sci. USA 108, E192–E194 (2011). source
- cites [2] Kirch, P. V. On the Road of the Winds (Univ. of California Press, 2017). source
- cites [4] Schmid, M. M. E. et al. How 14C dates on wood charcoal increase precision when dating colonization: the examples of Iceland and Polynesia. Quat. Geochronol. 48, 64–71 (2018). source
- Findingcitation
Many sampled individuals, including all samples from certain islands, have some non-Polynesian ancestry from European, Native American, and African sources.
“many individuals, including all samples from certain islands, have some amount of non-Polynesian ancestry: European, Native American, and African32.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [32] Wang, C. et al. Comparing spatial maps of human population-genetic variation using procrustes analysis. Stat. Appl. Genet. Mol. Biol. 9, 13 (2010). source
The Introduction discusses geographic patterns of genetic variation and compares SNP and CNV data, but does not report non-Polynesian ancestry in island samples. Searches for Polynesian ancestry and island admixture found no passage addressing the claimed European, Native American, and African sources. (LLM, conf=0.72)
Experimental — accuracy not yet measured
- Interpretationcitation
The East Asian ancestry observed in the Marquesas is likely due to post-colonial movement of Hakka immigrants from China for work in the 19th century.
“(This is likely due to the post-colonial movement to those islands of Hakka immigrants from China for work in the 19th century64.)”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [64] O’Connell, J. et al. A general approach for haplotype phasing across the full spectrum of relatedness. PLoS Genet. 10, e1004234 (2014). source
The Materials and Methods section (‘Real datasets’; page unavailable) describes cohorts in Europe and Uganda, not the Marquesas. Searches for Hakka immigration and East Asian ancestry in the Marquesas found no passage in our copy addressing the claimed explanation. (LLM, conf=0.76)
Experimental — accuracy not yet measured
- Premisecitation
The length distribution of fragments inherited from an ancestor T generations ago is exponential with decay rate λ = T.
“Hence, the distribution of the length of fragments (x) from a particular ancestor T generations ago will be exponential with λ = T decay rate97, fx=λe−λx.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [97] Botigué, L. R. et al. Gene flow from North Africa contributes to differential human genetic diversity in southern Europe. Proc. Natl Acad. Sci. USA 110, 11791–11796 (2013). source
The Results section (‘Long identical-by-descent haplotypes’; page unavailable) says that segments sharing a recent common ancestor have lengths and distributions informative of recent migration. It does not state that their lengths follow an exponential distribution or that the decay rate equals T generations. (LLM, conf=0.78)
Experimental — accuracy not yet measured
- Study design and conductcitation
Unknown distances can be imputed using the ultrametric inequality by finding the minimum over intermediate populations of the maximum of the two known distances.
“Using the ultrametric inequality, we can impute unknown distances d(i,j) simply by searching across all intermediate populations k and finding the minimum103, mink∈pops{max{di,k,dj,k}}.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [103] Deemer, W. L. Jr & Votaw, D. F. Jr Estimation of parameters of truncated or censored exponential distributions. Ann. Math. Stat. 26, 498–504 (1955). source
The Summary (p. 1) describes estimation for truncated and censored exponential distributions, and the Maximum-likelihood estimators section (pp. 2–3) develops those estimators. Searches for the ultrametric inequality and for imputing population distances through an intermediate population found no passage addressing the claimed method. (LLM, conf=0.75)
Experimental — accuracy not yet measured
- Premisecitation
The average number of pairwise differences between populations correlates more strongly with their divergence time than the outgroup-F3 statistic does.
“since πij has been shown to have higher correlation with the divergence time between two populations (i and j) than the outgroup-F3 statistic81”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [81] Peter, B. M. & Slatkin, M. The effective founder effect in a spatially expanding population. Evolution 69, 721–734 (2015). source
The Results (Range Expansion Model and Overview of Theoretical Results; page unavailable) discuss the directionality index ψ and geographic distance, not the relative correlations of πij and outgroup-F3 with divergence time. Searches for outgroup-F3, pairwise differences, and πij found no passage addressing that comparison. (LLM, conf=0.74)
Experimental — accuracy not yet measured
- Premisecitation
IBD length distributions are right-truncated at 15 cM because longer outlier segments are expected to come from recent contact less than 10 generations ago.
“The distributions are also right truncated at 15 cM, because outlier segments longer than this are expected to stem from recent contact, dating to less than 10 generations ago (18th century or later) as computed from the expected generation time (g) based on a single fragment length ℓ in Morgans, Egℓ≃32ℓ/1M, where 1M is one Morgan91.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [91] Edmonds, J. Optimum branchings. J. Res. Natl. Bur. Stand. 71B, 233–240 (1967). source
Section 4 describes an algorithm for maximum-weight branchings in directed graphs, and Section 2 discusses spanning arborescences; neither addresses genetic segments. Searches for IBD, 15 cM, centimorgans, and generation time found no passage supporting the truncation or dating claim. (LLM, conf=0.79)
Experimental — accuracy not yet measured
- Premisecitation
Identity-by-descent fragments shorter than 5 cM are prone to false positives because of insufficient SNPs.
“Fragments shorter than this length are prone to false positives due to insufficient SNPs90–92.”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [90] Chu, Y. J. & Lui, T. H. On the shortest arborescence of a directed graph. Science Sinica 14, 1396–1400 (1965).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [91] Edmonds, J. Optimum branchings. J. Res. Natl. Bur. Stand. 71B, 233–240 (1967). source
Section 3 describes an algorithm for optimum branchings in weighted graphs, and Section 9 discusses spanning arborescences; page numbers are unavailable in our copy. Searches for identity-by-descent fragments, 5 cM, SNPs, and false positives found no passage addressing the claim. (LLM, conf=0.78)
Experimental — accuracy not yet measured - cites [92] Ceballos, F. C., Joshi, P. K., Clark, D. W., Ramsay, M. & Wilson, J. F. Runs of homozygosity: windows into population history and trait architecture. Nat. Rev. Genet. 19, 220–234 (2018). source
- Findingown data
The Polynesian migration sequence was a serial founder expansion characterized by directional loss of variants.
“Our reconstruction of the branching Polynesian migration sequence reveals a serial founder expansion, characterized by directional loss of variants”
Quote in the paperSubstantial claim - Findingown data
The first two dimensions of major genomic variation do not separate Polynesian islands geographically.
“the first two dimensions of major genomic variation—even in an ancestry-specific PCA of the Polynesian individuals (Fig. 1b)—do not separate islands geographically”
Quote in the paperSubstantial claim - Findingreasoning
Polynesian islands differ widely in genetic diversity.
“the Polynesian islands differ widely in genetic diversity.”
Quote in the paperSubstantial claim - Findingreasoning
The settlement path of Polynesia can be reconstructed using the directionality-based algorithm.
“Using this more robust directionality-based algorithm (see Supplementary Discussion ‘On tree-building’), the settlement path of Polynesia can be reconstructed (Fig. 2a).”
Quote in the paperSubstantial claim - Findingown data
In ancestry-specific tSNE, western ancestral islands group on the left and more recently settled eastern islands on the right.
“In a plot of this ancestry-specific tSNE method (Fig. 1d), the islands of the ancestral west—Taiwan, Island Southeast Asia (Sumatra), Fiji, Tonga, and Samoa—are grouped on the left and the more recently settled eastern islands on the right.”
Quote in the paperSubstantial claim - Findingreasoning
Minor alleles on isolated Pacific islands were lost in a telescoping fashion following colonization order due to successive founding bottlenecks.
“We confirm this hypothesis below”
- Also stated in: § Discussion · boosted
“The modern peoples of Polynesia carry strong genetic evidence for a range expansion beginning in Samoa and propagating out across eastern Polynesia through a series of telescoping founder events from the 11th through 12th centuries.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · boosted
- Findingown data
Islands within archipelagos form neighboring clusters in ancestry-specific tSNE.
“Islands in archipelagos, for instance the Cook Islands of Mauke, Atiu, and Rarotonga, form neighboring clusters.”
Quote in the paperNot a substantial claim - Findingown data
The population of Raivavae arrived via the distant Tuamotus and Mangareva, not via the other Austral islands Tubuai and Rimatara.
“Notably, we find that the population of Raivavae in the Australs arrived via the distant Tuamotus and Mangareva, rather than via the other Austral islands of Tubuai and Rimatara (Fig. 1a and Supplementary Figs. 6, 7).”
Quote in the paperSubstantial claim - Findingcitation
Later divergence dates (1330-1360 CE) for North Marquesas (Nuku Hiva), Raivavae, and Rimatara fall within the period of greatest inter-island trade contact in eastern Polynesia.
“Our later divergence dates (1330–1360 CE) for some islands within archipelagos—North Marquesas (Nuku Hiva) in the Marquesas, Raivavae and Rimatara in the Australs—fall within the period of greatest inter-island trade contact in eastern Polynesia25.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [25] Kirch, P. V. et al. Human ecodynamics in the Mangareva Islands: a stratified sequence from Nenega-Iti Rock Shelter (site AGA-3, Agakauitai Island). Archaeol. Oceania 50, 23–42 (2015). source
- Findingown data
Five ancestries-African, European, Native American, Ni-Vanuatuan, and Remote Oceanian-were indicated within the Pacific island samples by the K = 7 ADMIXTURE clustering.
“The existence of these five ancestries within the Pacific island samples had been indicated by the K=7 unsupervised global ADMIXTURE clustering run discussed above (Supplementary Fig. 32).”
Quote in the paperSubstantial claim - Findingown data
Both masking methods, using either Taiwan or Tonga, Samoa, and Fiji as the outgroup, produced the same ordering of islands settled.
“However, both masking methods (both the Taiwan and the Tonga, Samoa, Fiji outgroup polarizations) gave the same ordering of islands settled.”
Quote in the paperNot a substantial claim - Findingown data
The modern peoples of Polynesia carry strong genetic evidence for a range expansion beginning in Samoa and propagating across eastern Polynesia through telescoping founder events from the 11th through 12th centuries.
“The modern peoples of Polynesia carry strong genetic evidence for a range expansion beginning in Samoa and propagating out across eastern Polynesia through a series of telescoping founder events from the 11th through 12th centuries.”
Quote in the paperSubstantial claim - Findingown data
South Marquesas, Fatu Hiva, was settled early, around 1140 CE, from Palliser.
“South Marquesas (Fatu Hiva) was, we have found, settled early (1140 CE) from Palliser.”
Quote in the paperSubstantial claim - Findingown data
The correction factors adjust the estimates by only a few percent.
“showing that these correction factors represent an adjustment of only a few percent.”
Quote in the paperNot a substantial claim - Findingown data
The F4 analysis found no significant internal cross-migration edges.
“The lack of significant internal cross-migration edges was determined by our F4 analysis above.”
Quote in the paperSubstantial claim - Findingown data
Only three branches in the settlement sequence show statistically significant deviations from the settlement model.
“Only three branches in our settlement sequence show any significant deviations”
Quote in the paperNot a substantial claim - Findingown data
Rapa Nui has the lowest heterozygosity among the islands.
“Rapa Nui also has the lowest heterozygosity (Supplementary Fig. 31)”
Quote in the paperSubstantial claim - Findingown data
Each of those significant deviations indicates a migration from Tahiti to an outlying French Polynesian island.
“each of these indicate a migration from Tahiti to an outlying French Polynesian island”
Quote in the paperSubstantial claim - Findingown data
Rapa Nui has the highest intra-island identity-by-descent.
“and the highest intra-island IBD (Supplementary Figs. 25–26)”
Quote in the paperSubstantial claim - Interpretationreasoning
The genetic composition of each remote island group is dominated by the contribution of its founders.
“that the genetic composition of each remote island group is dominated by the contribution of its founders (see Extended Data Figure 3)”
Quote in the paperSubstantial claim - Interpretationown data
After the Society Islands, the expansion reached the western Austral Islands and the Tuāmotu Archipelago in the 12th century.
“the western Austral (Tuha’a Pae) Islands and Tuāmotu Archipelago (12th century)”
Quote in the paperSubstantial claim - Premisecitation
The timing of Polynesian settlement is disputed, with different archaeological surveys differing by several centuries.
“Currently, several centuries separate the dates suggested by different archaeological surveys2–4.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [2] Kirch, P. V. On the Road of the Winds (Univ. of California Press, 2017). source
- cites [3] Mulrooney, M. A., Bickler, S. H., Allen, M. S. & Ladefoged, T. N. High-precision dating of colonization and settlement in East Polynesia. Proc. Natl Acad. Sci. USA 108, E192–E194 (2011). source
- cites [4] Schmid, M. M. E. et al. How 14C dates on wood charcoal increase precision when dating colonization: the examples of Iceland and Polynesia. Quat. Geochronol. 48, 64–71 (2018). source
- Premisecitation
The settlement sequence of Polynesian islands is difficult to resolve using comparative linguistic or cultural approaches because of rapid initial expansion and later cultural exchanges.
“The settlement sequence of Polynesian islands remains particularly difficult to unravel using comparative linguistic or cultural approaches due to the rapidity of the initial expansion and the subsequent cultural exchanges between islands7,9–11.”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [7] Kirch, P. V. & Green, R. C. Hawaiki, Ancestral Polynesia (Cambridge Univ. Press, 2001). source
- cites [9] Gray, R. D., Drummond, A. J. & Greenhill, S. J. Language phylogenies reveal expansion pulses and pauses in Pacific settlement. Science 323, 479–483 (2009). source
- cites [10] Walworth, M. Eastern Polynesian: the linguistic evidence revisited. Ocean. Linguist. 53, 256–272 (2014). source
- cites [11] Martinsson-Wallin, H., Wallin, P. & Anderson, A. Chronogeographic variation in initial East Polynesian construction of monumental ceremonial sites. J. Island Coastal Archaeol. 8, 405–421 (2013). source
- Interpretationown data
The expansion spread first through the Cook Islands, specifically Rarotonga.
“that originated in Samoa and spread first through the Cook Islands (Rarotonga)”
Quote in the paperSubstantial claim - Study design and conductnone given
The directionality-based tree-building algorithm is guaranteed to find the optimal tree in the presence of perfect data.
“is guaranteed to find the optimal tree out of the space of all possible trees in the presence of perfect data”
Quote in the paperNot a substantial claim - Interpretationown data
The serial founder expansion originated in Samoa.
“that originated in Samoa and spread first through the Cook Islands (Rarotonga)”
Quote in the paperSubstantial claim - Interpretationown data
Large-scale post-colonial admixture confounds Polynesian-focused interpretations of within- and between-island variance when admixed samples are included in PCA.
“The presence of large-scale post-colonial admixture from such divergent ancestry sources completely confounds Polynesian-focused interpretations of within-island and between-island variance when these admixed samples are included in the PCA (Supplementary Fig. 4).”
Quote in the paperSubstantial claim - Interpretationown data
Standard non-ancestry-specific analyses are confounded by recent colonial ancestry even when its proportion is small.
“standard non-ancestry specific analyses are confounded by the recent introduction of highly differentiated colonial ancestry, such as European, even when that ancestry proportion is small (Supplementary Fig. 10).”
Quote in the paperSubstantial claim - Study design and conductown data
The tSNE pattern is consistent across alternate dimensionality reduction methods, including UMAP, SOM, and genetic drift projection.
“This pattern is consistent across alternate dimensionality reduction methods (see Methods), including our ancestry-specific formulations of uniform manifold approximation (UMAP) (Supplementary Figs 6, 7) and self-organizing map (SOM) (Supplementary Fig. 8), as well as our genetic drift projection method (Supplementary Fig. 9).”
Quote in the paperNot a substantial claim - Interpretationreasoning
IBD-based divergence dates should be interpreted as terminus ante quem for settlement of each child island.
“Nevertheless, these divergence dates should be seen as the terminus ante quem for the settlement of each child island (Fig. 2A and Extended Data Table 1 and Extended Data Fig. 6).”
Quote in the paperSubstantial claim - Interpretationown data
After Rarotonga, the expansion reached the Society Islands in the 11th century.
“then to the Society (Tōtaiete mā) Islands (11th century)”
Quote in the paperSubstantial claim - Interpretationreasoning
For remote islands such as Rapa Nui with no large-scale population exchanges, IBD-based dates should closely match actual settlement dates.
“In the case of the most remote islands such as Rapa Nui, which are believed to have had no large-scale population exchanges with other islands, the IBD-based date should coincide closely with the actual date of settlement.”
Quote in the paperSubstantial claim- Rests on an assumption: Rapa Nui had no large-scale population exchanges with other islands.
- Interpretationreasoning
Among recently settled Polynesian islands, genetic drift is created mainly by founder effects rather than time.
“amongst the relatively recently settled Polynesian islands, genetic drift is created not so much by time, but by founder effects.”
Quote in the paperSubstantial claim - Interpretationreasoning
The largely un-drifted parental populations for most Polynesian islands are still extant and are the populations of the originating islands.
“Thus, the largely un-drifted (parental) populations for most of these islands are still extant: they are the populations of the originating islands.”
Quote in the paperSubstantial claim - Premisecitation
Polynesia was settled through a series of long ocean voyages across a region spanning about one third of the globe.
“Polynesia was settled in a series of extraordinary voyages across an ocean spanning one third of the planet1”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1] Low, S. Hawaiki Rising: Hōkūle‘a, Nainoa Thompson, and the Hawaiian Renaissance (Univ. of Hawaii Press, 2019).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
When Taiwan was used as the outgroup, small Ni-Vanuatuan segments within Polynesia were masked because they trace predominantly to a Papuan outgroup in New Guinea rather than to Austronesian Taiwan.
“When using Taiwan as an outgroup, we masked the small Ni-Vanuatuan segments seen within Polynesia, since these segments trace their predominant ancestral origin back to a Papuan outgroup in New Guinea, rather than to the Austronesian outgroup, Taiwan.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Averaging an individual's two haplotype vectors into one genotype frequency vector fills in much of the masked data missing from either haplotype.
“By explicitly averaging an individual’s two haplotype vectors to form a single genotype frequency vector for that individual, we are able to fill in much of the masked data that is missing from either of the two haplotypes.”
Quote in the paperSubstantial claim - Study design and conductreasoning
European, African, and Native American chromosomal segments were removed from the Pacific island samples before Polynesian ancestry-specific analyses.
“For this reason we removed European chromosomal segments, as well as African and Native American, from the Pacific island samples.”
Quote in the paperSubstantial claim - Interpretationown data
From Mangareva, the expansion reached Rapa Nui around 1210 CE.
“From Mangareva, we find that the expansion reached the easternmost inhabited Polynesian island, Rapa Nui (Easter Island), around 1210 CE.”
Quote in the paperSubstantial claim - Interpretationreasoning
The inferred dates and settlement path support the idea that expansion into eastern Polynesia was mediated by the emergence of intermediary island clusters around the turn of the last millennium.
“Thus, our inferred dates and settlement path lend support to the idea that expansion into eastern Polynesia was mediated by the birth of those intermediary island clusters at the turn of the last millennium.”
Quote in the paperSubstantial claim - Interpretationreasoning
The larger sample size from Tonga, Samoa, and Fiji compared with Taiwan allowed a more permissive bound for confirming minor alleles in the outgroup, increasing the number of markers used.
“The larger number of samples from Tonga, Samoa, and Fiji (51), as opposed to Taiwan (22), also contributed, as it allowed us to set a more permissive bound for confirming that an allele observed minor in the outgroup samples was also minor in the outgroup population.”
Quote in the paperNot a substantial claim - Interpretationreasoning
This supports the theory that Native American contact occurred while Polynesians were embarking on their easternmost and longest voyages of discovery.
“This supports the theory that that contact occurred while the Polynesians were embarking on their easternmost, and longest, voyages of discovery.”
Quote in the paperSubstantial claim - Study design and conductown data
The settlement sequence is supported by multiple marker frequency-based genetic analyses.
“This settlement sequence is also supported by our marker frequency-based genetic analyses, including ancestry-specific UMAP (Supplementary Fig. 6), drift projection (Supplementary Fig. 9), F-statistics (Supplementary Figs. 11–12), principal curve analyses (Extended Data Fig. 7 and Supplementary Fig. 17), diversity statistics (Supplementary Figs. 25–31), and ADMIXTURE clustering (Supplementary Figs”
Quote in the paperSubstantial claim - Premisereasoning
In highly related populations, including serially founded small island groups, identity-by-descent analyses are powerful for reconstructing migrations.
“In such cases, for example serially founded small island populations, IBD-based analyses become a powerful tool for reconstructing migrations.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [89] Davison, A. C. & Hinkley, D. V. Bootstrap Methods and Their Application (Cambridge Univ. Press, 1997). source
- Study design and conductreasoning
The shape of the IBD length distribution is not affected by errors in estimating each population's ancestry fraction.
“Although the total count (integral) of this distribution will be influenced by the fraction in each population of the ancestry of interest, the shape of the distribution will not be.”
Quote in the paperSubstantial claim - Interpretationreasoning
To first order, the decay rate λ measures the time since the parent and child islands split plus a constant.
“Thus, to first order the decay rate parameter λ will measure the time (T/50 with T in generations) to the split of the parent and child islands plus a constant”
Quote in the paperSubstantial claim- The authors state this as an assumption: The constant added to the parent-child split time in the decay rate λ is common across these remote islands and founder events.
- Premisenone given
The normalized total length of IBD sharing between two populations is sensitive to accurate estimation of the average fraction of the ancestry of interest in each population.
“although the normalized total length of IBD sharing between two populations gives a measure of the relatedness of the populations, it is quite sensitive to an accurate estimation of the average fraction in each population of the ancestry of interest.”
Quote in the paperSubstantial claim - Interpretationreasoning
Two present-day individuals, one from a child island and one from its parent island, cannot share a common ancestor in their Polynesian ancestry segments more recently than the child island's founding date.
“A pair of present-day Pacific islanders, one from the child island and one from the parent island, cannot share a common ancestor at any site (in their Polynesian ancestry segments) more recently than the founding date of the child island.”
Quote in the paperSubstantial claim - Study design and conductreasoning
The frequency of non-productive recombination events can be corrected using a factor ρ, the average intra-island IBD proportion, applied separately to each branch of the pedigree.
“Therefore, we can correct for the frequency of these non-productive recombination events at each meiosis event. The correction factor ρ (the proportion of the genome shared on average intra-island) is specific to each island (dependent on the intra-island IBD on each island accrued through preceding founding bottlenecks) and so must be applied separately to the two branches of the pedigree”
Quote in the paperSubstantial claim - Premisecitation
Coop et al. showed that the decay rate parameter λ of the IBD length distribution is a weighted average of the distribution of times to the most recent common ancestor across genomic sites.
“Coop et. al have shown that the decay rate parameter λ of this distribution is a weighted average of the distribution of times to the most recent common ancestor across all genomic sites99.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [99] Jobling, M., Hurles, M. & Tyler-Smith, C. Human Evolutionary Genetics (Garland Science, 2013). source
- Interpretationreasoning
For dating the founding of an isolated island group, the demographic conditions make the inverse problem tractable.
“However, for our problem—dating the founding of an isolated island group—the demography is amenable.”
Quote in the paperSubstantial claim - Premisecitation
Inter-island IBD segments that lie entirely within post-colonial ancestries, or that span post-colonial and pre-colonial ancestries, must result from post-colonial inter-island contact.
“Inter-island IBD segments lying wholly within post-colonial ancestries, or spanning post-colonial and pre-colonial ancestries, are necessarily the result of post-colonial inter-island contact events and were discarded.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [65] D’Arcy, P. The Chinese Pacifics: a brief historical review. J. Pacific Hist. 49, 396–420 (2014). source
- Study design and conductreasoning
The sum of IBD lengths is not robust to errors in ancestry normalization.
“However, the sum of IBD lengths, which is the integral of the curves in Supplementary Fig. 22A, is clearly not robust to such errors in the normalization (rescaling the y-axis).”
Quote in the paperNot a substantial claim
- May combine two claims. 61
- Classified as probably not a substantial claim. 32
May combine two claims.
PremisecitationAncient DNA studies of Polynesia have sequenced only four samples from one western Polynesian island and three near-modern samples from one eastern Polynesian island, with low genotype density and limited overlap.
“Meanwhile, ancient DNA studies have sequenced only four samples from one island in western Polynesia and three near-modern samples from one island in eastern Polynesia, all with low genotype density, still lower between-sample genotype overlap, and different time frames17,18.”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [17] Skoglund, P. et al. Genomic insights into the peopling of the Southwest Pacific. Nature 538, 510–513 (2016). source
The paper’s ancient-DNA passage (section labeled Abstract; page unavailable) explicitly places its four sequenced individuals on two islands: three on Efate, Vanuatu, and one on Tongatapu, Tonga—not four on one western Polynesian island. It reports 139,461–231,944 covered SNPs per individual, but does not report three near-modern eastern Polynesian samples or the claimed between-sample genotype overlap. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured - cites [18] Posth, C. et al. Language continuity despite population replacement in Remote Oceania. Nat. Ecol. Evol. 2, 731–740 (2018). source
The Results (‘Different genetic trajectory in Polynesia’; page unavailable) report three genome-wide samples from Ra’iātea, eastern Polynesia, dated to the 18th century. The paper also reports three Tongan samples, but does not establish the claimed total of four western Polynesian samples from one island; nor does it state that all samples had low genotype density or quantify between-sample overlap. (LLM, conf=0.84)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationStandard errors for all allele-frequency-based statistics were computed using a block bootstrap with 100 replicates and a block size of 1000 markers.
“Standard errors for all allele frequency based statistics were computed using the block-bootstrap using 100 replicates and a block size of 1000 markers86.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [86] Patterson, N. et al. Reconstructing Indian population history. Nature 461, 489–494 (2009). source
The Methods Summary (page not available in our copy) says standard errors were computed using a Block Jackknife, not a block bootstrap. It does not give the claimed 100 replicates or 1,000-marker block size. (LLM, conf=0.89)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationPrevious region-wide Polynesian genetics studies were limited to globin gene polymorphisms, near Polynesia, or the Society Islands, and lacked an ancestry-specific approach.
“Previous region-wide Polynesian genetics studies have considered only globin gene polymorphisms14, or have been restricted to near (western) Polynesia15 and the Society Islands16 and lacked an ancestry-specific approach.”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [14] Hill, A. V. S. et al. Polynesian origins and affinities: globin gene variants in eastern Polynesia. Am. J. Hum. Genet. 40, 453–463 (1987).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [15] Wollstein, A. et al. Demographic history of Oceania inferred from genome-wide data. Curr. Biol. 20, 1983–1992 (2010). source
- cites [16] Hudjashov, G. et al. Investigating the origins of eastern Polynesians using genome-wide data from the Leeward Society Isles. Sci. Rep. 8, 1823 (2018). source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationGeological analyses of Polynesian trade goods, especially adzes, indicate that remote Polynesian islands remained in trade contact for several centuries.
“Geological analyses of Polynesian trade goods, particularly adzes, indicate that the remote Polynesian islands remained in trade contact with one another for several centuries25,28,29.”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites [25] Kirch, P. V. et al. Human ecodynamics in the Mangareva Islands: a stratified sequence from Nenega-Iti Rock Shelter (site AGA-3, Agakauitai Island). Archaeol. Oceania 50, 23–42 (2015). source
- cites [28] Weisler, M. I. et al. Cook Island artifact geochemistry demonstrates spatial and temporal extent of pre-European interarchipelago voyaging in East Polynesia. Proc. Natl Acad. Sci. USA 113, 8150–8155 (2016). source
- cites [29] Collerson, K. D. & Weisler, M. I. Stone adze compositions and the extent of ancient Polynesian voyaging and trade. Science 317, 1907–1911 (2007). source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPolynesians are predominantly descended from Austronesian-speaking voyagers.
“The Polynesians are predominantly descended from Austronesian-speaking voyagers17”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [17] Skoglund, P. et al. Genomic insights into the peopling of the Southwest Pacific. Nature 538, 510–513 (2016). source
The paper’s ancestry-model passage (labelled Abstract in our copy; no page given) identifies a population related to the First Remote Oceanians as the primary component in present-day Polynesians, and describes seafaring settlement of Remote Oceania. It does not establish that those ancestral voyagers spoke Austronesian languages; the Extended Data table labels some present-day sampled populations Austronesian-speaking, but not the ancient voyagers. (LLM, conf=0.82)
Experimental — accuracy not yet measured
May combine two claims.
FindingcitationThe inferred settlement date for Rapa Nui is consistent with Wilmshurst and Mulrooney and agrees closely with Hunt et al.'s 1200 CE date and recent radiocarbon dates.
“Our date for the settlement of Rapa Nui is consistent with Wilmshurst and Mulrooney and also agrees closely with the date found by Hunt et al. (1200 CE) based on analyses of pollen in lake cores and soil erosion patterns42, as well as with recent radiocarbon dates of archaeological sites43.”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [42] Anderson, A. J., Conte, E., Smith, I. & Szabo, K. New excavations at Fa’ahia (Huahine, Society Islands) and chronologies of central East Polynesian colonization. J. Pac. Arch. 10, 1–14 (2019). source
The Radiocarbon Dating Results from Fa’ahia section describes dates from Huahine, while General points discusses colonization estimates for other East Polynesian island groups. Searches for Rapa Nui or Easter Island settlement, Wilmshurst, Mulrooney, and Hunt’s 1200 CE estimate found no passage assessing the claimed agreement with Rapa Nui archaeological dates. (LLM, conf=0.74)
Experimental — accuracy not yet measured - cites [43] Hunt, T. L. & Lipo, C. P. Evidence for a shorter chronology on Rapa Nui (Easter Island). J. Island Coast. Archaeol. (2008). source
Classified as probably not a substantial claim. May combine two claims.
PremisecitationArchaeological estimates for Polynesian settlement dates are debated and have recently been revised forward across eastern Polynesia by up to a millennium.
“Meanwhile, the archaeological estimates for settlement dates remain debated, and have recently been revised forward across eastern Polynesia by up to a millennium2–4,12,13.”
Quote in the paperSubstantial claim1 of 5 sources checked- cites [2] Kirch, P. V. On the Road of the Winds (Univ. of California Press, 2017). source
- cites [3] Mulrooney, M. A., Bickler, S. H., Allen, M. S. & Ladefoged, T. N. High-precision dating of colonization and settlement in East Polynesia. Proc. Natl Acad. Sci. USA 108, E192–E194 (2011). source
- cites [4] Schmid, M. M. E. et al. How 14C dates on wood charcoal increase precision when dating colonization: the examples of Iceland and Polynesia. Quat. Geochronol. 48, 64–71 (2018). source
- cites [12] Wilmshurst, J. M., Hunt, T. L., Lipo, C. P. & Anderson, A. J. High-precision radiocarbon dating shows recent and rapid initial human colonization of East Polynesia. Proc. Natl Acad. Sci. USA 108, 1815–1820 (2011). source
The introduction says East Polynesian settlement dates remain debated, with long and short chronologies differing by 400–1,000 years. The Results and Discussion report a revised, later colonization chronology, but say it shortens the estimated age by up to 2,000 years relative to some earlier claims. Thus the stated ceiling of a millennium does not capture the full range reported by this source. (LLM, conf=0.84)
Experimental — accuracy not yet measured - cites [13] Spriggs, M. & Anderson, A. Late colonization of east Polynesia. Antiquity 67, 200–217 (1993). source
May combine two claims.
InterpretationreasoningThe matrix completion method used permits all samples, not only a reference panel, to be used for completion, which allows more accurate completion.
“Unlike earlier methods69, this method permits the use of all samples, rather than only a panel of reference samples, for the completion step; thus, far more data is used allowing for more accurate completion.”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [32] Wang, C. et al. Comparing spatial maps of human population-genetic variation using procrustes analysis. Stat. Appl. Genet. Mol. Biol. 9, 13 (2010). source
The Introduction describes Procrustes analysis for comparing spatial maps, including plots whose sample sets only partially overlap. Searches for matrix completion, reference panels, missing entries, and imputation found no passage about using all samples in a completion step or improving completion accuracy. Page numbers were not provided in our copy. (LLM, conf=0.75)
Experimental — accuracy not yet measured - cites [68] Moreno-Estrada, A. et al. The genetics of Mexico recapitulates Native American substructure and affects biomedical traits. Science 344, 1280–1285 (2014). source
The passage on reference panels (section labeled Abstract; page unavailable) concerns haplotype sharing in Mexican samples, not a matrix-completion method. Searches for matrix completion, the completion step, and missing-data imputation found no passage saying that all samples can be used for completion or that doing so improves accuracy. (LLM, conf=0.76)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationNative American ancestry entered Polynesia particularly through emigration of admixed Hispanic individuals from Chile, which annexed Rapa Nui, and African ancestry also entered.
“Native American ancestry, particularly from emigration of admixed Hispanic individuals from Chile, which annexed Rapa Nui (Easter Island), and African ancestry also entered32.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [32] Wang, C. et al. Comparing spatial maps of human population-genetic variation using procrustes analysis. Stat. Appl. Genet. Mol. Biol. 9, 13 (2010). source
The Introduction discusses comparisons of genetic-variation maps and CNV datasets, but does not address ancestry entering Polynesia. Searches for Rapa Nui, Chilean migration, Native American ancestry, and African admixture found no passage supporting the claim in our copy. (LLM, conf=0.76)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationThe block bootstrap gives better variance estimates than the jackknife for these pairwise allele frequency comparisons.
“This gives better variance estimates than the jackknife for these pairwise allele frequency comparisons34.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [34] Novembre, J. et al. Genes mirror geography within Europe. Nature 456, 98–101 (2008). source
The Methods Summary describes leave-one-out cross-validation, and the Methods describe SNP filtering and association simulations. Neither those passages nor searches for “block bootstrap,” “jackknife,” and “variance estimates” address a comparison of the two methods for pairwise allele-frequency comparisons. (LLM, conf=0.75)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataRequiring a minor allele frequency of 0.1 or lower in the merged Tonga, Samoa, and Fiji outgroup yielded 228,262 SNPs, whereas requiring minor alleles to be fixed in the Taiwan outgroup yielded 137,383 SNPs.
“(A 0.1 or lower minor allele frequency was required in the merged Tonga, Samoa, Fiji outgroup samples, yielding 228,262 SNPs, as opposed to the more stringent requirement of minor alleles being fixed in the Taiwan outgroup samples, following the procedure of Zhan et. al37, which yielded only 137,383 SNPs.)”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [37] Peter, B. M. & Slatkin, M. Detecting range expansions from genetic data. Evolution 67, 3274–3289 (2013). source
The Results > Application section describes an analysis of human populations using several hundred thousand loci, but gives neither of the claimed SNP counts. Searches for the Tonga–Samoa–Fiji and Taiwan outgroups, the two counts, and the stated allele-frequency criteria found no passage addressing those filters. (LLM, conf=0.76)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationEuropean ancestries entered Polynesia during the colonial period, beginning with Magellan in the 16th century and with significant immigration starting in the early 19th century.
“European ancestries entered Polynesia during the colonial period with the first European explorer (Magellan) arriving in the 16th century and significant immigration commencing in the early 19th century64.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [64] O’Connell, J. et al. A general approach for haplotype phasing across the full spectrum of relatedness. PLoS Genet. 10, e1004234 (2014). source
The Materials and Methods section (‘Real datasets’; page unavailable) describes cohorts in Europe and Uganda, while the other retrieved passages concern haplotype phasing or references. Searches for Polynesia, Magellan, colonial-era European ancestry, and 19th-century immigration found no passage in our copy addressing the claim. (LLM, conf=0.77)
Experimental — accuracy not yet measured
May combine two claims.
Interpretationown dataThe Tuamotu Archipelago served as a regional voyaging hub from which settlers moved north to the Marquesas and south to the Gambier Islands beginning in the mid-1100s CE.
“Stretching across central eastern Polynesia, the Tuamotu Archipelago was previously hypothesized to have served as a regional voyaging hub20,25,28, and our analysis indicates that it was from this hub that settlers made their way north to the Marquesas Islands (Nuku Hiva and Fatu Hiva in our dataset) and south to the Gambier Islands (Mangareva in our dataset) beginning in the mid-1100s CE.”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [20] Emory, K. P. The Tuamotuan creation charts by Paiore. J. Polynesian Soc. 48, 1–29 (1939).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [25] Kirch, P. V. et al. Human ecodynamics in the Mangareva Islands: a stratified sequence from Nenega-Iti Rock Shelter (site AGA-3, Agakauitai Island). Archaeol. Oceania 50, 23–42 (2015). source
- cites [28] Weisler, M. I. et al. Cook Island artifact geochemistry demonstrates spatial and temporal extent of pre-European interarchipelago voyaging in East Polynesia. Proc. Natl Acad. Sci. USA 113, 8150–8155 (2016). source
May combine two claims.
FindingcitationPre-colonial Native American genetic contact is identified only on islands inferred to have been settled via the Tuamotus, and its timing corresponds closely with voyaging dates for the region.
“It is also notable that it is only on islands that we infer were settled via the Tuamotus that pre-colonial Native American genetic contact has been identified, and its timing corresponds closely with our voyaging dates for this region32.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [32] Wang, C. et al. Comparing spatial maps of human population-genetic variation using procrustes analysis. Stat. Appl. Genet. Mol. Biol. 9, 13 (2010). source
The Introduction compares worldwide genetic and geographic maps using Procrustes analysis; it does not discuss settlement through the Tuamotus. Searches for Native American genetic contact, Polynesian islands, and voyaging dates found no passage addressing the claimed locations or timing. (LLM, conf=0.78)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationAdmixture between Papuan and Austronesian source populations occurred on Vanuatu and other Melanesian islands in the thousand years before Polynesian settlement and was carried into Polynesia during settlement.
“(Admixture between populations stemming from these two sources occurred on Vanuatu and other Melanesian islands in the thousand years before the settlement of Polynesia and was carried into Polynesia during its settlement17,79.)”
Quote in the paperSubstantial claim2 of 2 sources checked- cites [17] Skoglund, P. et al. Genomic insights into the peopling of the Southwest Pacific. Nature 538, 510–513 (2016). source
The paper’s Abstract (page unavailable) dates Papuan–First Remote Oceanian mixture to roughly 1,500–2,300 years before present and finds Papuan ancestry in present-day Polynesians. It does not locate that mixture on Vanuatu or other Melanesian islands, or establish that an already admixed population carried it into Polynesia during settlement. Instead, the ancient Vanuatu and Tongan individuals had little or no Papuan ancestry, and the paper infers later movements into Remote Oceania. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [79] Wittek, P., Gao, S. C., Lim, I. S. & Zhao, L. Somoclu: an efficient parallel library for self-organizing maps. J. Stat. Softw. 78, https://doi.org/10.18637/jss.v078.i09 (2017). source
The Introduction (pp. 1–2) discusses self-organizing maps, not population history. Searches for admixture on Vanuatu and other Melanesian islands, and for Papuan–Austronesian ancestry and Polynesian settlement, found no passage in our copy addressing the claim. (LLM, conf=0.78)
Experimental — accuracy not yet measured
Classified as probably not a substantial claim.
PremisecitationThe model of IBD segment independence holds only when population size N is much greater than the number of generations T.
“In addition, the model of IBD segment independence holds only for (N >> T) with N the population size and T the number of generations97.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [97] Botigué, L. R. et al. Gene flow from North Africa contributes to differential human genetic diversity in southern Europe. Proc. Natl Acad. Sci. USA 110, 11791–11796 (2013). source
The Results section discusses detecting and comparing IBD segments, and Materials and Methods describes a sample-size correction. Neither states when IBD segments can be treated as independent; searches for segment independence and the N >> T condition found no supporting passage. Page numbers were not available in our copy. (LLM, conf=0.73)
Experimental — accuracy not yet measured
May combine two claims.
PremisereasoningFor IBD segments shared by two present-day individuals from a common ancestor, the decay rate λ is 2T, or T/50 when lengths are measured in centimorgans.
“If we are considering recombination segments shared between two present day individuals stemming from the same common ancestor, that is IBD segments, we must adjust the rate for the number of recombination events per unit length that have occurred down both sides of the pedigree from this common ancestor, which gives a λ of 2T total92,95,98.”
Quote in the paperSubstantial claim2 of 3 sources checked- cites [92] Ceballos, F. C., Joshi, P. K., Clark, D. W., Ramsay, M. & Wilson, J. F. Runs of homozygosity: windows into population history and trait architecture. Nat. Rev. Genet. 19, 220–234 (2018). source
- cites [95] Gusev, A. et al. Whole population, genome-wide mapping of hidden relatedness. Genome Res. 19, 318–326 (2009). source
- cites [98] Atzmon, G. et al. Abraham’s children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern ancestry. Am. J. Hum. Genet. 86, 850–859 (2010). source
May combine two claims.
PremisecitationThe recursive method for constructing the branching settlement path is an instance of the Chu-Liu-Edmonds algorithm, which guarantees a minimum spanning tree for a directed acyclic graph.
“This recursive algorithm for building the branching settlement path of the Pacific islands is a form of the Chu-Liu-Edmonds algorithm, which is guaranteed to produce the minimum spanning tree of a directed acyclic graph (see Supplementary Discussion ‘On tree-building’)87,88.”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [87] Bhatia, G., Patterson, N., Sankararaman, S. & Price, A. L. Estimating and interpreting FST: the impact of rare variants. Genome Res. 23, 1514–1521 (2013). source
The Methods section on Nei’s FST and the Results sections on SNP ascertainment and FST estimators discuss population-genetic estimates, not settlement-path construction. Searches for the Chu-Liu-Edmonds algorithm, Pacific Islands tree-building, and directed graphs found no passage in our copy addressing the claim. (LLM, conf=0.78)
Experimental — accuracy not yet measured - cites [88] Nei, M. & Roychoudhury, A. K. Sampling variances of heterozygosity and genetic distance. Genetics 76, 379–390 (1974). source
May combine two claims.
Findingown dataThe inferred dates differ from archaeological dates only for the Marquesas Island group and the Southern Cook Islands, where they are earlier.
“Only in the settlement of the Marquesas Island group, dated by Mulrooney to the late 1100s CE, and the Southern Cook Islands, dated even later by Wilmshurst to the mid-1200s CE, do we find different (earlier) dates.”
Quote in the paperSubstantial claimMay combine two claims.
FindingreasoningOriginating islands have much greater genetic diversity and dominate the first principal component when included in PCA.
“Because the originating islands have much greater diversity (as discussed below), they dominate the first principal component when included in the PCA (Supplementary Fig. 3).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataPolynesian population structure exhibits high dimensionality and is not reflective of geography.
“we find that Polynesian population structure exhibits high dimensionality (Supplementary Fig. 1) not at all reflective of geography (Fig. 1a)”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataRarotonga and Palliser appear at the center of eastern Polynesian islands, with other eastern islands radiating out from them.
“Rarotonga and Palliser appear at the center of the eastern Polynesian islands with the other eastern islands radiating out from them.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
FindingcitationProjections onto fewer dimensions gave similar results, with some clusters beginning to disappear between 12 and 15 dimensions, as predicted by the Tracy-Widom analysis.
“(Projections onto fewer dimensions yielded similar results, with some clusters beginning to disappear in the range 12–15 dimensions, as predicted by the Tracy-Widom analysis.)”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Findingown dataFiltering sites not located in Polynesian segments for any individual removed 60,377 SNPs, or 8.75% of 689,899 SNPs, leaving 629,522 SNPs for population allele frequency statistics.
“This filtering resulted in the loss of 60,377 SNPs (8.75% of the total 689,899 SNPs), leaving 629,522 SNPs across all populations for computation of population allele frequency statistics.”
Quote in the paperSubstantial claimMay combine two claims.
FindingreasoningUsing Tonga, Samoa, and Fiji as an outgroup reduced standard errors for the range expansion statistic on eastern Polynesian islands, while the general ordering of islands was the same as with the Taiwan outgroup.
“The latter calculation reduced the standard errors for the range expansion statistic on islands settled subsequent to western Polynesia, i.e. the eastern Polynesian islands; nevertheless, the general ordering of islands in the range expansion was the same for both calculations (see comparison Supplementary Fig. 14).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataModern Pacific islanders are often admixed, carrying European ancestry and occasionally Native American and African ancestries.
“As discussed above, modern Pacific islanders are often admixed, possessing European and occasionally Native American and African ancestries (Supplementary Fig. 32).”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationThe inferred settlement dates for Fatu Hiva (1140 CE) and the Tuamotus (1110 CE) agree with genealogical oral histories.
“our settlement dates (1140 CE on Fatu Hiva in the Marquesas, or 28.4 generations before 1989) agree with the genealogical oral histories of many Pacific islanders themselves (1005 CE, or 29 generations before 1875, on Fatu Hiva) 27. In the Tuamotus our dates (1110 CE, or 29.3 generations before 1989) agree even more closely with island’s oral histories (1125 CE, or 28 generations before 1965)44.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] Handy, E. S. C. The Native Culture in the Marquesas (The Bishop Museum, 1923).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [44] Mulrooney, M. A. An island-wide assessment of the chronology of settlement and land use on Rapa Nui (Easter Island) based on radiocarbon data. J. Archaeol. Sci. 40, 4377–4399 (2013). source
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataA few Pacific island individuals, especially in the Marquesas, had more than 5% East Asian ancestry in the ADMIXTURE results.
“A few Pacific island individuals, particularly in the Marquesas, were found to also have >5% East Asian ancestry in the ADMIXTURE results.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataF4 tests found deviations from the settlement tree only for three branches: Mangareva-Raivavae with migration from Tahiti, Mangareva-Palliser with migration from Tahiti, and North Marquesas-Palliser with migration from Tahiti and also from the Cooks.
“We find deviations from our settlement tree only for 3 of its branches: Mangareva – Raivavae (migration from Tahiti), Mangareva – Palliser (migration from Tahiti), and North Marquesas – Palliser (migration from Tahiti and also from the Cooks).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataCross-validation error showed an elbow at K = 7 ancestry clusters, with larger numbers of clusters giving little improvement.
“An elbow61 was found in the cross-validation error plot at K = 7 clusters, with larger numbers of clusters delivering little improvement (Supplementary Fig. 32).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe terminal islands in the settlement sequence have high levels of homozygosity and significant IBD.
“We have shown that these particular islands also have high levels of homozygosity (Supplementary Figs. 25–27), which should increase the power to detect trait associations, and significant IBD, enabling IBD mapping, another useful approach51.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [51] Buck Te Rangi Hīroa, P. H. Vikings of the Sunrise (J. B. Lippincott, 1938).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Findingown dataThe genotype frequency matrix had 14 significant dimensions, determined using a Tracy-Widom distribution and verified with a scree plot.
“The number of significant (p > 0.05) dimensions for the genotype frequency matrix, described above, was determined (n = 14) using a Tracy-Widom distribution57 and verified via a scree plot70.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe estimated λ values confirm the drift statistics: Mangareva is the most recently connected island to Rapa Nui, and Samoa is the most archaic connection.
“The pattern confirms the results of our drift statistics; Mangareva is the island most recently connected to Rapa Nui, while Samoa, the root of the expansion into remote Polynesia, is the most archaic connection.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataIBD sharing tends to increase along the inferred settlement chain, but the signal contains substantial noise.
“Trends of increasing IBD sharing along the course of the inferred settlement chain (see the map in Extended Data Fig. 5) are evident, but there is significant noise.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingreasoningRemoving outlier inter-island IBD segments does not significantly change the estimated island settlement dates but increases the standard error.
“Not removing these outliers does not change our island settlement dates significantly, but, by distorting the tail of the exponential decay distributions, does increase our standard error”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataRapa Nui has the largest ψ value, indicating it has the most potential parent islands and is terminal in the range expansion.
“Begin with the island with the most potential parents (at the end of the range expansion) (Fig. 2B) or in other words the largest ψ, Rapa Nui.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataRemoving λ entries with standard errors above 0.07 yields a more precise generation matrix but leaves some missing entries.
“Removing all entries corresponding to λ values that have standard errors above .07 (representing errors larger than 15% of the average λ value), creates a matrix of more precise generation values, but with some missing entries.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataUsing the outgroup-F3 metric instead of the pairwise difference metric yields the same settlement sequence.
“although the same settlement sequence is also returned when using the latter metric instead (Supplementary Fig. 12)”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataThe expansion finally reached the Marquesas, Raivavae, and Easter Island, with Easter Island settled around 1200 CE via Mangareva.
“finally to the widely separated, but genetically connected, megalithic statue-building cultures of the Marquesas (Te Henua ‘Enana) Islands in the north, Raivavae in the south, and Easter Island (Rapa Nui), the easternmost of the Polynesian islands, settled in approximately 1200 CE via Mangareva.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe Austronesian-speaking settlers of Fiji, Tonga, and Samoa populated the widely dispersed islands to their east through long voyages.
“The Austronesian-speaking settlers of the western Pacific (Fiji, Tonga, and Samoa) went on to people the widely dispersed islands in the vast ocean to their east through extraordinary voyages of exploration and settlement2,20.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [2] Kirch, P. V. On the Road of the Winds (Univ. of California Press, 2017). source
- cites [20] Emory, K. P. The Tuamotuan creation charts by Paiore. J. Polynesian Soc. 48, 1–29 (1939).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAustronesian linguistic origins trace to Taiwan.
“who trace their linguistic origins to Taiwan9”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [9] Gray, R. D., Drummond, A. J. & Greenhill, S. J. Language phylogenies reveal expansion pulses and pauses in Pacific settlement. Science 323, 479–483 (2009). source
May combine two claims.
Study design and conductreasoningRecent inter-island movement can introduce longer IBD segments and shift divergence time estimates toward the present, so a truncated exponential was fitted.
“Recent movement between islands, such as post-settlement trade contact, can introduce small numbers of longer, inter-island IBD segments, shifting the estimated divergence time towards the present, so we fit a truncated exponential.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataEach successive principal component captures genetic drift of a particular island or island group, indicating that genetic variance between islands is dominated by founder effects rather than diffusion clines or migration gradients.
“Instead, each successive principal component captures the genetic drift of a particular island or island group (Fig. 1b, c and Supplementary Fig. 2), illustrating that genetic variance between these islands is dominated by their founder effects, not by diffusion clines or migration gradients.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningThe dataset contains both terminal and internal nodes of the population tree, and their hierarchy is known from the ψ-statistic.
“When constructing a population tree, this means that our dataset contains not only the terminal (leaf) nodes, but also the internal nodes, and we know their hierarchy from the ψ-statistic.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductown dataQuality control filters removed individuals with more than 1% missing genotypes, sites missing in more than 1% of individuals, and 18 SNPs with extreme Hardy-Weinberg equilibrium deviations.
“Quality control filters were applied across all sampled individuals using the Plink 1.9 package53, removing individuals with >1% of genotyped sites missing (mind .01), removing genotyped sites missing in >1% of individuals (geno .01), and removing sites (18 SNPs) with extreme deviations from Hardy-Weinberg equilibrium (p-value less than 10e-110).”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductown dataIndividuals with a kinship coefficient greater than 0.2, indicating first-degree relatives, were iteratively removed.
“REAP55 was used to determine kinship coefficients using the ADMIXTURE clustering results discussed below; individuals with a kinship coefficient of >.2 (first degree relatives) were iteratively removed.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThe final leg to Rapa Nui had been suggested by linguistic similarities between Mangarevan and Rapanui and by similarities in traditional stone ceremonial platforms.
“This final leg had been suggested by some based on similarities between the Mangarevan and Rapanui languages48, and by similarities in their traditional stone ceremonial platforms49.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Interpretationown dataSettlers fanned out from Rarotonga northeast to the Society Islands around 1050 CE, and thence to the Tuamotu Archipelago by 1110 CE.
“Settlers also fanned out from Rarotonga northeast to the Society Islands (represented by Tahiti in our dataset but also containing the culturally significant island Raʻiātea) around 1050 CE, thence northeast to the Tuamotu Archipelago (represented by Mataiva in the Palliser group in our dataset) by 1110 CE.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenLocal approvals for engagement with the Rapa Nui community were obtained from the mayor of Easter Island, and the study was registered with CONADI under indigenous law No. 19.253.
“Local approvals for engagement with the Rapa Nui community were obtained from the mayor (Pedro Pablo Edmunds Paoa) of the municipality of Easter Island, and the study was registered with the National Corporation for Indigenous Development (CONADI), in accordance with the indigenous law No. 19.253.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenThe UNESCO International Declaration on Human Genetic Data and the Declaration of Helsinki were followed throughout the study.
“The guidelines of the UNESCO International Declaration on Human Genetic Data and the Declaration of Helsinki were followed throughout the study.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningThe reconstruction of the settlement path is independent of the date estimates and is more robust to later sporadic contact than IBD distributions.
“Note that our reconstruction of the settlement path is independent of these date estimates, which are overlaid upon it, and is more robust to later sporadic contact than IBD distributions are”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenNo statistical methods were used to predetermine sample size.
“No statistical methods were used to predetermine sample size.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataThe study was approved by the Council of Polynesian Elders for the Rapa Nui community and by local educational institutions.
“This study was also approved by the Council of Polynesian Elders for the community of Rapa Nui, along with local educational institutions, including the Lyceum Hoŋa’a o te Mana and the Lorenzo Baeza school for adults.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe Tuamotu hub and other critical atolls had only recently emerged above falling sea levels (900 CE) and finished solidifying topsoil and forests.
“At this time the widely scattered Tuamotu hub and other critical atolls in the expansion path (e.g. Nororotu in the Austral group), would have only recently emerged above falling sea levels (900 CE) and finished solidifying their topsoil and forests44,47”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [44] Mulrooney, M. A. An island-wide assessment of the chronology of settlement and land use on Rapa Nui (Easter Island) based on radiocarbon data. J. Archaeol. Sci. 40, 4377–4399 (2013). source
- cites [47] Walworth, M. The Language of Rapa Iti (Univ. Hawaii, 2015).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Interpretationown dataFrom Rarotonga, settlers continued south around 1190 CE to Rapa Iti and separately east to the smaller Cook Islands (Mauke and Atiu).
“From this base, we find that settlers continued south around 1190 CE to Rapa Iti (a branch recently hypothesized from linguistic evidence46) and, separately, east to the smaller Cook Islands (Mauke and Atiu in our dataset).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [46] Di Piazza, A., Di Piazza, P. & Pearthree, E. Sailing virtual canoes across Oceania: revisiting island accessibility. J. Archaeol. Sci. 34, 1219–1225 (2007). source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationRarotonga's clouds made it visible from long distances and probably facilitated its discovery.
“These clouds on its prominent mountain make the island visible for long distances at sea and probably facilitated its discovery45.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Pirazzoli, P. A. & Montaggioni, L. F. Late Holocene sea-level changes in the northwest Tuamotu islands, French Polynesia. Quat. Res. 25, 350–368 (1986). source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenAfter merging reference and sample genotype data, unambiguous strand inconsistencies were flipped and ambiguous SNPs were removed, leaving 689,899 SNP sites.
“After merging reference sequence data with sample genotyped data, strand inconsistencies were flipped when unambiguous, while ambiguous SNPs were removed, leaving 689,899 SNP sites.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataResearch ethics approval and permits were obtained from Stanford University IRB, Oxford University Tropical Research Ethics Committee, and the Scientific Ethics Committee of the Catholic University of Chile.
“research/ethics approval and permits were obtained from the following institutions: Stanford University Institutional Review Board (IRB approval No. 20839), Oxford University Tropical Research Ethics Committee (reference No. 537–14), and the Scientific Ethics Committee of the Catholic University of Chile (reference No. 1971092).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThe average genotype call rate was 98.5% for all newly genotyped samples.
“The average call rate was 98.5% for all newly genotyped samples.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataWritten informed consent was obtained from every participant in the study.
“Written informed consent was obtained from all participants”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenCommunity engagement, including pre-participation presentations and post-participation return of results, was conducted throughout the project.
“Community engagement, including pre-participation presentations and post-participation return of results, were conducted throughout the project.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningBecause allele frequencies drifted during settlement, some alleles minor in Taiwan became major by western Polynesia, so repolarizing with Tonga, Samoa, and Fiji increased resolution and reduced standard errors for downstream islands.
“Because allele frequencies drifted during the Pacific island settlement process, some minor alleles in Taiwan would have become major alleles by the time the settlers reached western Polynesia (see Supplementary Discussion ‘On psi‘), so the intermediate repolarization using Tonga, Samoa, and Fiji as an outgroup increased the resolution of the range expansion statistic (reduced standard errors) for”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningA genome-wide haplotype vector assembled by concatenating chromosomes switches phase arbitrarily at chromosome boundaries and is therefore already a mixture of an individual's two true parental haplotypes.
“Thus, a genome-wide haplotype vector constructed by assembling all chromosomes sequentially into a single row vector will switch phase arbitrarily across chromosome boundaries and so is already a mixture of an individual’s two true parental haplotypes.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationAncestries introduced through colonial settlement did not necessarily follow the same island settlement process, founder sizes, or dates as original Polynesian settlement, so they must be distinguished from Polynesian ancestry.
“Because ancestries fully (or partially) introduced via colonial settlement did not necessarily follow the same island settlement process (or founder sizes and dates) as the original Polynesian settlement, such ancestries need to be distinguished, necessitating an ancestry-specific approach65, cf. Supplementary Figs. 10, 20.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [65] D’Arcy, P. The Chinese Pacifics: a brief historical review. J. Pacific Hist. 49, 396–420 (2014). source
May combine two claims.
Interpretationown dataRaivavae, North and South Marquesas, and Rapa Nui share a common genetic source in the Tuamotu archipelago and had monumental stone statue traditions.
“Together with even more distant North and South Marquesas and Rapa Nui, each also with inferred settlement stemming from the Tuamotus, Raivavae had an ancient tradition of carving monumental anthropomorphic statues in stone. No other Austral island had these50; indeed, such immense sculptures are found only on those far-flung islands that we now, however, show to had a common genetic source in the”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [50] Flenley, J. & Bahn, P. The Enigmas of Easter Island (Oxford Univ. Press, 2003).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Interpretationown dataFrom western Polynesia, voyagers reached Rarotonga around 830 CE, passing from Samoa along a route shared with Fiji and Tonga.
“From western Polynesia, Polynesian voyagers reached Rarotonga in the Cook Islands around 830 CE, having passed from Samoa along a route shared with the settlement of Fiji and Tonga.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationreasoningBecause drift is independent among separated small island populations, some deviation from Hardy-Weinberg equilibrium is expected in Polynesia, so a typical Hardy-Weinberg threshold was not applied.
“The independence of drift between these separated, small island populations leads us to expect some deviation from Hardy-Weinberg in Polynesia, so we do not apply a typical threshold here.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenThe experiments were not randomized and investigators were not blinded to allocation during experiments and outcome assessment.
“The experiments were not randomized and the investigators were not blinded to allocation during experiments and outcome assessment.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataThe dataset has T values of 25-30 generations and N values in the thousands, so it avoids the problematic regimes for the IBD model.
“Fortunately, our dataset has T values of 25–30 generations and N values in the thousands21, so we do not fall into these problematic regimes.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [21] Hunt, T. & Lipo, C. The Statues that Walked (Free Press, 2011).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
Interpretationown dataThe Tahiti migrations align with Tahiti's recent role as the capital of French Polynesia.
“consistent with Tahiti’s recent role as the capital of French Polynesia.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Premisenone givenThe per-generation recombination rate is constant over time, so the distance from an ancestral population to any sampled contemporary descendant is the same when measured by segment length distributions.
“This works because the per generation recombination rate is constant over time, so the distance from an ancestral population to any of its sampled contemporary descendants is the same when measured by segment length distributions.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisereasoningThe decay rate of the IBD length distribution changes steadily each generation and does not depend on unknown fluctuations in historical population sizes.
“In addition, the shape of the IBD length distribution (decay rate) changes steadily each generation. It does not depend, as genetic drift does, on the fluctuations, which are generally unknown, of the historical population sizes.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationThe Poisson process model of recombination holds for small IBD segments (T > 5), but for more recent relatedness the finite size of chromosomes must be considered.
“The model of a Poisson process of recombination events along a continuous genome holds for small IBD segment lengths, viz. T > 5, but for more recent relatedness, leading to very long IBD segments, one must consider the finite size of the chromosomes themselves when computing the IBD length distribution101.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [101] Palamara, P. F., Lencz, T., Darvasi, A. & Pe'er, I. Length distributions of identity by descent reveal fine-scale demographic history. Am. J. Hum. Genet. 91, 809–822 (2012). source
May combine two claims.
Study design and conductown dataChanging the ancestry normalization factor alters the amplitude but not the decay rate λ of the exponential IBD length distribution, showing that λ is robust to ancestry normalization errors.
“This alters the amplitude, but not the decay rate shape parameter λ, of the exponential in Supplementary Fig. 22A, or, equivalently, the intercept, but not the slope of the lines in Supplementary Fig. 22B; thus demonstrating graphically that λ is robust to noise (errors) in ancestry normalization.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataFounding bottlenecks create some intra-island IBD, causing some recombination events to be non-productive.
“However, because of the founding bottlenecks for each island, there is some intra-island IBD shared between pairs of individuals on the island (Supplementary Figs. 25, 26), so some recombination events will be non-productive.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningThe ultrametric inequality holds because all samples are contemporary and are leaf nodes of the ancestry tree dating to the present.
“This holds in our case because all samples were taken from contemporary populations, and so all are leaf nodes of the ancestry tree dating to the same period (the present).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationMarkers were bootstrapped together as long contiguous blocks to preserve the effects of linkage on the variance of the estimates.
“The markers are bootstrapped together as long contiguous blocks to preserve the effects of linkage on the variance of the estimates35.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [35] Nei, M. & Kumar, S. Molecular Evolution and Phylogenetics (Oxford Univ. Press, 2000). source
May combine two claims.
Study design and conductreasoningThe migration graph is acyclic, a result derived from the formal definition of ψ.
“That our graph is acyclic can be shown (proof derived in Supplementary Discussion ‘On the acyclicity of psi’) from the formal definition of ψ, which defines our edge directionality.”
Quote in the paperSubstantial claim
The paper relies on this without support.
The order in which Polynesian islands were settled was unknown before this study.
“but the sequences of islands settled remain unknown and their timings disputed.”
The paper relies on this without support.
Little was known about the human genetic structure of Polynesia before this study.
“little is known about the human genetic structure of this oceanic expanse”
The paper relies on this without support.
Rapa Nui had no large-scale population exchanges with other islands.
“which are believed to have had no large-scale population exchanges with other islands”
The paper relies on this without support.
The sampled individuals are representative of their island populations.
“using genome-wide data from merely 430 contemporary individuals from 21 key Pacific island populations”
The authors state this as an assumption.
Recombination occurs without interference.
“Assuming no interference, recombination can be modeled as a Poisson process occurring along the genome at a rate of one recombination break per generation per unit of genomic length (measured in Morgans) 96.”
The authors state this as an assumption.
The constant added to the parent-child split time in the decay rate λ is common across these remote islands and founder events.
“which we assume is common for these remote islands and founder events and calibrate empirically, see Extended Data Table 1”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The ancient individuals remained most closely related to present-day Rapanui even when a broader set of Oceanian reference individuals was considered.
“Concordantly, the ancient individuals remained most closely related to present-day Rapanui even when we considered a broader set of Oceanian reference individuals7,39 (Supplementary Fig. 12, Supplementary Table 5 and Supplementary Information section 7).”
From Ancient Rapanui genomes reveal resilience and pre-European contact with the Americas (2024) · cites this paper as [39]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Stated F4 calculation does not include one of its four populations
MinorThe printed formula for F4(A,B;C,D) contains no frequency for population D. As written, changing D cannot change the statistic, despite the paper's stated use of it to test whether A and B form a separate clade from C and D.
“the F4 statistic was computed for each site using the formula of Patterson et al.35 F^4A,B;C,D=p~A−p~Cp~B−p~C”
“The F4 statistic is expected to be zero unless groups A, B do not form a separate clade from C, D within the actual population tree.”
Expansion period excludes the stated arrival at Rarotonga
MinorThe discussion places the expansion from Samoa to Rarotonga around 830 CE, in the ninth century. That falls outside the later description of the expansion as occurring from the eleventh through twelfth centuries.
“a range expansion beginning in Samoa and propagating out across eastern Polynesia through a series of telescoping founder events from the 11th through 12th centuries.”
“From western Polynesia, Polynesian voyagers reached Rarotonga in the Cook Islands around 830 CE, having passed from Samoa along a route shared with the settlement of Fiji and Tonga.”
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Gene flow from North Africa contributes to differential human genetic diversity in southern Europe
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Self-citationNative American gene flow into Polynesia predating Easter Island settlement
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Self-citationThe Great Migration and African-American Genomic Diversity
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Self-citationPacific Atoll Living: How Long Already and Until When
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Eastern Polynesian: The Linguistic Evidence Revisited
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Identification of Pedigree Relationship from Genome Sharing
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Cited by
Sorted by citations
Greenacre, M. J., Groenen, P. J. F., Hastie, T. J., D’Enza, A. I., Markos, A., & Tuzhilina, E. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00184-w · Cited by 1,936 · see citing works
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“…profiles of Polynesian, Rapa Nui, and Maori population samples to those of Taiwanese populations are further examples of the capacity of HLA data to detect these sequential, long-range migration patterns as previously noted (Friedlaender et al., 2008; Riccio et al., 2013; Ioannidis et al., 2021).”
BackgroundThe Role of Genome Sequencing in Neonatal Intensive Care Units
Kingsmore, S. F., & Cole, F. S. (2022) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-120921-103442 · Cited by 95 · see citing works
A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes
Bastard, P., Hsiao, K., Zhang, Q., Choin, J., Best, E., Chen, J., Gervais, A., Bizien, L., Materna, M., Harmant, C., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20220028 · Cited by 70 · see citing works
“However, the variant was present in the Austral Islands ( n = 211, AF = 0.00474), the Society Islands ( n = 764, AF = 0.000654), the Marquesas Islands ( n = 199, AF = 0.00251), the Cook Islands ( n = 70, AF = 0.0143), and Fiji ( n = 24, AF = 0.0208; Fig.”
BackgroundMethodInfluentialSelf-citationGenomic perspectives on human dispersals during the Holocene
Stoneking, M., Arias, L., Liu, D., Oliveira, S., Pugach, I., & Rodriguez, J. J. R. B. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2209475119 · Cited by 35 · see citing works
“Other studies suggested back migrations from Polynesia (121) and native American ancestry that arrived in Polynesia before European contact (122), although the latter relies on analyses of modern samples and so far has not received any support from ancient DNA (123).”
Rye: genetic ancestry inference at biobank scale
Conley, A. B., Rishishwar, L., Ahmad, M., Sharma, S., Norris, E. T., Jordan, I. K., & Mariño‐Ramírez, L. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad149 · Cited by 28 · see citing works
Deep history of cultural and linguistic evolution among Central African hunter-gatherers
Padilla‐Iglesias, C., Blanco-Portillo, J., Pricop, B., Ioannidis, A. G., Bickel, B., Manica, A., Vinicius, L., & Migliano, A. B. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01891-y · Cited by 40 · see citing works
“24,82, reference panels for each ancestry cluster were created by selecting unadmixed agriculturalist and CAHG individuals (with >98% agriculturalist-or CAHG-associated ancestry) indicated by the unsupervised global ADMIXTURE K = 2 (ref.”
InfluentialSelf-citationHyperuricaemia and gout in the Pacific
Gérard, B., Leask, M., Merriman, T. R., Bardin, T., Oehler, E., Lawrence, A., Viali, S., Ofanoa, S., Karu, L. T., Stamp, L. K., et al. (2025) · Nature Reviews Rheumatology · doi:10.1038/s41584-025-01228-7 · Cited by 35 · see citing works
“Subsequent studies suggest serial migrations expanding between unoccupied archipelagos, with a final expansion to Rapa Nui (Easter Island) and Aotearoa New Zealand approximately 800 years ago 72–74 .”
SALAI-Net: species-agnostic local ancestry inference network
Sàbat, B. O., Montserrat, D. M., Giró-i-Nieto, X., & Ioannidis, A. G. (2022) · Bioinformatics · doi:10.1093/bioinformatics/btac464 · Cited by 22 · see citing works
Self-citationAncient Rapanui genomes reveal resilience and pre-European contact with the Americas
Moreno-Mayar, J. V., Sousa da Mota, B., Higham, T., Klemm, S., Gorman Edmunds, M., Stenderup, J., Iraeta-Orbegozo, M., Laborde, V., Heyer, E., Torres Hochstetter, F., et al. (2024) · Nature · doi:10.1038/s41586-024-07881-4 · Cited by 20 · see citing works
“Concordantly, the ancient individuals remained most closely related to present-day Rapanui even when we considered a broader set of Oceanian reference individuals 7,39 (Supplementary Fig.”
Chassagne, F., Butaud, J., Torrente, F., Conte, E., Ho, R., & Raharivelomanana, P. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115186 · Cited by 20 · see citing works
The genetic legacy of the Manila galleon trade in Mexico
Rodríguez-Rodríguez, J. E., Ioannidis, A. G., Medina-Muñoz, S. G., Barberena-Jonas, C., Blanco-Portillo, J., Quinto-Cortés, C. D., & Moreno‐Estrada, A. (2022) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2020.0419 · Cited by 11 · see citing works
“Population genetics studies have shed light on past historical events and demographic dynamics that in turn are associated with cultural influences [1,2].”
BackgroundSelf-citationTriumph of the Commons: Sustainable Community Practices on Rapa Nui (Easter Island)
DiNapoli, R. J., Lipo, C. P., & Hunt, T. L. (2021) · Sustainability · doi:10.3390/su132112118 · Cited by 12 · see citing works
Allen, M. S., Lewis, T., & Porch, N. (2022) · PLoS ONE · doi:10.1371/journal.pone.0265224 · Cited by 10 · see citing works
Boundary Effects Cause False Signals of Range Expansions in Population Genomic Data
Kemppainen, P., Schembri, R., & Momigliano, P. (2024) · Molecular Biology and Evolution · doi:10.1093/molbev/msae091 · Cited by 7 · see citing works
“Consistent with the literature (Peter and Slatkin 2013, 2015; He et al. 2017; Ioannidis et al. 2021), ψ and clines thereof were more sensitive to REs than statistics based on genetic diversity, yet in most cases, they remained highly correlated in equilibrium and nonequilibrium meta-populations…”
InfluentialUnderstanding the human settlement of the Pacific – Are we there yet?
Matisoo-Smith, E. A., & Gosling, A. L. (2025) · Journal of Archaeological Science · doi:10.1016/j.jas.2025.106307 · Cited by 9 · see citing works
Unravelling the determinants of human health in French Polynesia: the MATAEA project
Teiti, I., Aubry, M., Fernandes‐Pellerin, S., et al. (2023) · Frontiers in Epidemiology · doi:10.3389/fepid.2023.1201038 · Cited by 8 · see citing works
“Although archaeological and 89 linguistic data have provided evidence for the geographical and temporal origin of the populations of 90 the Eastern Pacific islands, the sequence and timings of settlement of the Polynesian islands are still 91 debated (3).”
BackgroundCultural Evolution of Central African hunter-gatherers reflects a deep history of interconnectivityPreprint
Padilla‐Iglesias, C., Blanco-Portillo, J., Ioannidis, A. G., Manica, A., Vinicius, L., & Migliano, A. B. (2022) · Research Square · doi:10.21203/rs.3.rs-2205369/v1 · Cited by 7 · see citing works
Self-citationLabuda, D., Harding, T., Milot, E., & Vézina, H. (2022) · PLoS ONE · doi:10.1371/journal.pone.0266079 · Cited by 7 · see citing works
“Likewise, the first arrivals from the Asiatic mainland to isolated Polynesian islands have experienced rapid initial growth, continued through a succession of founding bottlenecks, with resulting populations dominated by the genetic contribution of their founders [84].”
Wares, J. P., Thiel, M., Munizaga, M., et al. (2022) · Journal of Crustacean Biology · doi:10.1093/jcbiol/ruac054 · Cited by 7 · see citing works
Lynch, R., Loehr, J., Lummaa, V., Honkola, T., Pettay, J. E., & Vesakoski, O. (2022) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2021.2298 · Cited by 8 · see citing works
Ecological dynamics of moa extinctions reveal convergent refugia that today harbour flightless birds
Tomlinson, S., Lomolino, M. V., Wood, J. R., Anderson, A., Brown, S. C., Haythorne, S., Perry, G. L. W., Wilmshurst, J. M., Austin, J. J., & Fordham, D. A. (2024) · Nature Ecology & Evolution · doi:10.1038/s41559-024-02449-x · Cited by 6 · see citing works
“This rapid expansion of people across a third of the Earth’s surface 10 caused wide-scale population declines and extinctions of native insular biotas, disproportionately impacting endemic species, including hundreds of species of flightless birds 11 .”
The loss of biodiversity in Madagascar is contemporaneous with major demographic events
Alva, O., Leroy, A., Heiske, M., Pereda‐Loth, V., Tisseyre, L., Boland, A., Deleuze, J., Rocha, J., Schlebusch, C. M., Fortes‐Lima, C., et al. (2022) · Current Biology · doi:10.1016/j.cub.2022.09.060 · Cited by 7 · see citing works
Modern Polynesian genomes offer clues to early eastward migrations
Kirch, P. V. (2021) · Nature · doi:10.1038/d41586-021-01719-z · Cited by 6 · see citing works
Reciprocity, Risk, and Rivalry: Variability in Central East Polynesian Exchange Networks
Allen, M. S. (2025) · Journal of World Prehistory · doi:10.1007/s10963-025-09189-1 · Cited by 5 · see citing works
Modelling the impact of large-scale hydroclimate change on prehistoric Polynesian island life
Hipkiss, C. V., Sheffield, J., Langdon, P. G., & Sear, D. (2025) · Quaternary Environments and Humans · doi:10.1016/j.qeh.2025.100074 · Cited by 5 · see citing works
Native Hawaiian and Pacific Islander populations in genomic research
Ha, E. K., Shriner, D., Callier, S., Riley, L., Adeyemo, A., Rotimi, C. N., & Bentley, A. R. (2024) · npj Genomic Medicine · doi:10.1038/s41525-024-00428-6 · Cited by 6 · see citing works
“This migration history is characterized by directional loss of genetic variants along the branching routes in this vast network of islands 59 .”
BackgroundMonuments, Place Names and Black Lives Matter: Memorialising Captain James Cook
Moreton‐Robinson, A. (2022) · Legalities · doi:10.3366/legal.2022.0029 · Cited by 5 · see citing works
Leveraging known Pacific colonisation times to test models for the ancestry of Southeast Asians
Almeida, M., Gandini, F., Rito, T., Foody, M. G. B., Brandão, A., Oliveira, M., Olivieri, A., Fichera, A., Oteo‐García, G., Zainuddin, Z., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-20856-3 · Cited by 5 · see citing works
Pan-African model explains Homo sapiens genetic and morphological evolutionPreprint
Padilla‐Iglesias, C., Xue, Z., Leonardi, M., Perez, M. F., Paijmans, J. L. A., Colucci, M., Hovhannisyan, A., Delser, P. M., Blanco-Portillo, J., Ioannidis, A. G., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.22.655514 · Cited by 6 · see citing works
Self-citationDeep history of cultural and linguistic evolution among Central African hunter-gatherersPreprint
Padilla‐Iglesias, C., Blanco-Portillo, J., Pricop, B., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2666234/v1 · Cited by 4 · see citing works
Self-citationValentí Rull, A. (2023) · Plants · doi:10.3390/plants12112089 · Cited by 4 · see citing works
“Some recent studies point to a much later colonization wave (900–1200 CE) from western Polynesia (Samoa, Tonga) [97,112], and the topic is now under discussion [113].”
BackgroundInfluentialThe Oxford Handbook of Archaeology and Language
(2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.001.0001 · Cited by 4 · see citing works
Dallaire, X., Normandeau, É., Brazier, T., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.11.628006 · Cited by 3 · see citing works
Ancient DNA reveals rapid natural selection during the Black Death
Enard, D. (2022) · Nature · doi:10.1038/d41586-022-03160-2 · Cited by 3 · see citing works
Ocean variability drives a millennial-scale shift in South Pacific hydroclimate
Peaple, M. D., Skinner, D. T., Inglis, G. N., Joshi, M., Langdon, P. G., Matthews, A. J., Osborn, T. J., & Sear, D. (2025) · Communications Earth & Environment · doi:10.1038/s43247-025-02676-5 · Cited by 2 · see citing works
“The fi nal expansion by humans into Eastern Polynesia around 1000 years BP followed an ~1700-year pause during which distinct Poly-nesianculturedevelopedintheislandsofSamoaandTonga 44 .”
A genealogy-based approach for revealing ancestry-specific structures in admixed populations
Tang, J., & Chiang, C. W. K. (2025) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2025.06.016 · Cited by 2 · see citing works
McIvor, I. H., Hogg, A., Roa, T., Waitoki, W., Boswijk, G., Gumbley, W., Anderson, A., & McBride, R. (2025) · Archaeometry · doi:10.1111/arcm.13074 · Cited by 2 · see citing works
Computational analysis reveals historical trajectory of East Polynesian lunar calendars
Valério, M., Tamburini, F., & Corazza, M. (2026) · PLoS ONE · doi:10.1371/journal.pone.0353287 · Cited by 1 · see citing works
Historical comparative linguistics and language classification
Barlow, R., & Campbell, L. R. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.3 · Cited by 2 · see citing works
Bayesian phylogenetics for language prehistory— and archaeology
Heggarty, P., & Powell, A. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.11 · Cited by 2 · see citing works
Archaeolinguistics of the languages of the Andes
Urban, M., Barbieri, C., & Rademaker, K. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.33 · Cited by 1 · see citing works
Niger-Congo archaeolinguistics, including Bantu
Bostoen, K. A. G., Coutros, P. R., & Schlebusch, C. M. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.30 · Cited by 3 · see citing works
Archaeolinguistics of Papuan languages
Schapper, A., Gaffney, D., & Brucato, N. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.26 · Cited by 2 · see citing works
Indo-European archaeolinguistics
Lubotsky, A., & Pronk, T. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.18 · Cited by 1 · see citing works
Austronesian archaeolinguistics
Spriggs, M., Geraghty, P., & Liu, Y.-C. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.25 · Cited by 1 · see citing works
Vesakoski, O., Salmela, E., & Piezonka, H. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.19 · Cited by 2 · see citing works
A genealogy-based approach for revealing ancestry-specific structures in admixed populationsPreprint
Tang, J., & Chiang, C. W. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.10.632475 · Cited by 1 · see citing works
“The appropriate use of UMAP on human data is continually being explore (Diaz-Papkovich et al. 2023), and it may be more suitable in the context of exploring isolated islands where significant drift may occur, for instance (Ioannidis et al. 2021).”
Role of Genomics in Neonatal Care and Research—A Narrative Review
Kar, S. S., Dube, R., George, B. T., & Jhancy, M. (2024) · OBM Genetics · doi:10.21926/obm.genet.2404276 · Cited by 1 · see citing works
Galbraith, D. (2024) · Genealogy · doi:10.3390/genealogy8040129 · Cited by 1 · see citing works
“They allege—contrary to mainstream academic historical, archeological, and genetic studies (Bunbury et al. 2022; Wilmshurst et al. 2011; Ioannidis et al. 2021; Knapp et al. 2012)—that the Hotu arrived in Aotearoa during the 200s B.C., predating the first Polynesian arrivals by well over 1000 years.”
The Archaeology of East Polynesia
Kirch, P. V., & Molle, G. (2024) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780197607770.013.28 · Cited by 1 · see citing works
Alelyani, T. (2024) · Research Square · doi:10.21203/rs.3.rs-3741717/v1 · Cited by 1 · see citing works
Boundary effects cause false signals of range expansions in population genomic dataPreprint
Kemppainen, P., Schembri, R., & Momigliano, P. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.06.570483 · Cited by 1 · see citing works
Insights from ancient human DNA into the colonization of Oceania
Stoneking, M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99931-1.00144-6 · Cited by 1 · see citing works
Rull, V. (2023) · Preprints.org · doi:10.20944/preprints202304.1192.v1 · Cited by 1 · see citing works
Modelling speciation: Problems and implications
Bard, J. (2022) · In Silico Biology · doi:10.3233/isb-220253 · Cited by 2 · see citing works
“These methodologies, as applied to human mitochondrial DNA and other sequence data, have allowed us, for example, to discover details of the travels of H. sapiens over the past ∼ 65 Ky when early founder groups left Africa to populate the modern world (e.g. [89], for review, see [1]).”
MethodSobre el origen del poblamiento de Canarias
Delgado, J. A. D. (2026) · Gerión Revista de Historia Antigua · doi:10.5209/geri.106209
Interaction of migration and frequency dependence in cultural populations
Alvarez, N. P., Fogarty, L., & Kandler, A. (2026) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2026.112516
Revisiting Founder Populations in an Age of Global Biobanks
Caggiano, C., Shemirani, R., & Kenny, E. E. (2026) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-020525-034901
Benchmarking genetic birth prevalence estimates against newborn screening data
Sierant, M. C., Knoblauch, N., Witt, E., Gaffney, D. J., Pulit, S. L., & Wüster, A. (2026) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2026.04.002
“54,55 Fifth, those self-identified as “Hispanic,” “Latino,” “Native American,” or “American Indian” were matched to the AMR group in gnomAD.”
Hipkiss, C. V., Langdon, P. E., Sheffield, J., Leng, M. J., Temple-Brown, C., & Sear, D. (2026) · Quaternary Science Reviews · doi:10.1016/j.quascirev.2026.110006
A Tsallis-Entropy Lens on Genetic Variation
Geleta, M., Montserrat, D. M., & Ioannidis, A. G. (2026) · doi:10.1109/icassp55912.2026.11461540
“1) Polynesia: The consensus peopling model for East Poly-nesia (Cook Islands, French Polynesia) features rapid, late settlement following a serial founder expansion from West Polynesia (Samoa, Tonga) [22], [23].”
Self-citationMatisoo-Smith, E. A., Whitelaw, B., Collins, C., & Gosling, A. L. (2026) · Journal of Pacific Archaeology · doi:10.70460/jpa.v16i2.396
New insights from old DNA into the colonization of the Pacific: Two case studies
Stoneking, M. (2026) · Human Population Genetics and Genomics · doi:10.47248/hpgg2606010003
Alyokhin, A. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-28846-3.00010-5 · Cited by 1 · see citing works
Sierant, M. C., Knoblauch, N., Witt, E., et al. (2025) · medRxiv · doi:10.1101/2025.10.11.25337773
Coalescent theory of the ψ directionality index
Lappo, E., & Rosenberg, N. A. (2025) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkaf202 · Cited by 1 · see citing works
“Ioannidis et al. (2021) similarly used pairwise values of ψ be-tween pairs of human populations of different Pacific islands to understand sequences of events in the human settlement of the region.”
Robbeets, M. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.1
Guo, J., Fan, Z., Yang, W., & Wang, C. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.24
Iversen, R., & Riede, F. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.35
Palaeosiberian archaeolinguistics
Potter, B. A., & Vajda, E. J. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.21
Prehistoric language change in social context
Bakker, P. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.8
Pagel, M. D. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.2
Archaeolinguistics and the languages of hunter-gatherers
Evans, N. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.13 · Cited by 1 · see citing works
Transeurasian archaeolinguistics
Robbeets, M., Hudson, M. J., & Ning, C. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.20
Robbeets, M., & Hudson, M. J. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.37
The relationship between genetics, language, and culture
Mace, R. H. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.12
Epps, P. L., & Khanina, O. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.5
Evans, B. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.4
Archaeology and language change in the Bronze Age
Hudson, M. J., Bjørn, R., & Spengler, R. N. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.15
Dunn, M. G. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.7 · Cited by 1 · see citing works
Wichmann, S. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.6 · Cited by 2 · see citing works
Archaeology and language dynamics in the medieval and early modern eras
Hudson, M. J., Harland, J. M., & Crowther, A. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.17
Nilo-Saharan archaeolinguistics
Dimmendaal, G. J., & Babiker, H. M. A. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.29
Farming and language dispersals consequent upon the oldest developments of food production
Bellwood, P. S. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.14
Advances in population genetics and language history
Barbieri, C., & Widmer, P. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.36
Ancient states and the rise of writing
Haicheng, W. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.16
Sino-Tibetan archaeolinguistics
Bradley, D. T. C., Li, L., Ning, C., & Martello, R. D. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.22 · Cited by 3 · see citing works
The archaeolinguistics of Kalahari Basin area languages
Güldemann, T., Smith, A. B., & Bajić, V. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.31
Archaeolinguistics of language families and contact areas of Amazonia
van Gijn, R., Arias, L., & de Souza, J. G. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.34
Ehret, C., Schoenbrun, D. L., Brandt, S., & Keita, S. O. Y. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.28
Bowern, C., Llamas, B., Miceli, L., Tobler, R., & Veth, P. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.27 · Cited by 1 · see citing works
Wollen, J. T., El-Desoky, R., Rosario, N., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-7048958/v1
From ritual spaces to monumental expressions: rethinking East Polynesian ritual practices
Wallin, P., & Martinsson‐Wallin, H. (2025) · Antiquity · doi:10.15184/aqy.2025.10096 · Cited by 1 · see citing works
From ritual spaces to monumental expressions: rethinking East Polynesian ritual practices
Wallin, P., & Martinsson‐Wallin, H. (2025) · Antiquity · doi:10.15184/aqy.2025.96
(2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.002.0006
(2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.002.0011
Robbeets, M., & Hudson, M. J. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.002.0009
(2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.002.0004
(2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.002.0007
- Authors
- Ioannidis, A. G., Blanco-Portillo, J., Sandoval, K., Hagelberg, E., Barberena-Jonas, C., Hill, A. V. S., Rodríguez-Rodríguez, J. E., Fox, K., Robson, K., Haoa-Cardinali, S., Quinto-Cortés, C. D., Miquel-Poblete, J. F., Auckland, K., Parks, T., Sofro, A. S. M., Ávila-Arcos, M. C., Sockell, A., Homburger, J. R., Eng, C., Huntsman, S., Burchard, E. G., Gignoux, C. R., Verdugo, R. A., Moraga, M., Bustamante, C. D., Mentzer, A. J., & Moreno-Estrada, A.
- Affiliations
- Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (MX)
- University of Oslo (NO)
- Centre for Human Genetics (GB)
- University of California San Diego (US)
- University of Oxford (GB)
- Yarsi University (ID)
- Stanford University (US)
- University of California, San Francisco (US)
- University of Colorado Denver (US)
- University of Chile (CL)
- Corresponding author
- Ioannidis, Alexander G.
- ORCID
- Ioannidis, Alexander G.
- Blanco-Portillo, Javier
- Sandoval, Karla
- Hagelberg, Erika
- Barberena-Jonas, Carmina
- Hill, Adrian V. S.
- Rodríguez-Rodríguez, Juan Esteban
- Fox, Keolu
- Robson, Kathryn
- Quinto-Cortés, Consuelo D.
- Auckland, Kathryn
- Parks, Tom
- Sockell, Alexandra
- Homburger, Julian R.
- Eng, Celeste
- Huntsman, Scott
- Burchard, Esteban G.
- Gignoux, Christopher R.
- Verdugo, Ricardo A.
- Moraga, Mauricio
- Bustamante, Carlos D.
- Mentzer, Alexander J.
- Moreno-Estrada, Andrés
- Venue
- Nature
- Published
- 2021-09-22
- Volume
- 597
- Issue
- 7877
- Pages
- 522-526
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC9710236
- OpenAlex
- W3201145195
- Cited by
- 124
- References
- 116
- Citations by year
- 2026: 11 · 2025: 55 · 2024: 12 · 2023: 27 · 2022: 17 · 2021: 2
- FWCI
- 8.18
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Wellcome Trust (106289/Z/14/Z)
- National Institute for Health and Care Research (CL-2018-13-007)
- U.S. National Library of Medicine (T15LM007033)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Forensic and Genetic Research
- Social Sciences › Geography, Planning and Development › Pacific and Southeast Asian Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Keywords
- gene networks, Marquesas Islands, Raivavae, Easter Island, Mangareva, Cook Islands, Society Islands, Tuamotu Archipelago, Pacific Island populations, megalithic culture
- MeSH terms
- Pacific Island People, Female, Humans, Male, Polynesia, Genome, Human, Genomics, History, Medieval, Human Migration
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