Rp. Murraymcintosh et al., TESTING MIGRATION PATTERNS AND ESTIMATING FOUNDING POPULATION-SIZE INPOLYNESIA BY USING HUMAN MTDNA SEQUENCES, Proceedings of the National Academy of Sciences of the United Statesof America, 95(15), 1998, pp. 9047-9052
The hypervariable 1 region of human mtDNA shows markedly reduced varia
bility in Polynesians, and this variability decreases from western to
eastern Polynesia. Fifty-four sequences from New Zealand Maori show th
at the mitochondrial variability with just four haplotypes is the lowe
st of any sizeable human group studied and that the frequency of haplo
types is markedly skewed, The Maori sequences, combined with 268 publi
shed sequences from the Pacific, are consistent with a series of found
er effects from small populations settling new island groups. The dist
ributions of haplotypes were used to estimate the number of females in
founding population of New Zealand Maori. The three-step simulation u
sed a randomly selected founding population from eastern Polynesia, an
expansionary phase in New Zealand, and finally the random selection o
f 54 haplotypes. The results are consistent with a founding population
that includes approximate to 70 women (between 50 and 100), and sensi
tivity analysis shows that this conclusion is robust to small changes
in haplotype frequencies. This size is too large for models postulatin
g a very small founding population of ''castaways,'' but it is consist
ent with a general understanding of Maori oral history as well as the
results of recent canoe voyages recreating early trans-oceanic voyages
.