Table 2.
Population | Gene | N | Haplotypes (n) | S | h (± SD) | θs (± SD) | θπ (± SD) |
---|---|---|---|---|---|---|---|
YN | COII | 8 | 1(2), 3(2), 4(2), 5(1), 6(1) | 4 | 0.002 ± 0.002 | 1.543 ± 0.961 | 1.643 ± 1.227 |
Cytb | 13 | 1(2), 2(5), 4(3), 5(1), 6(1), 7(1) | 5 | 0.004 ± 0.003 | 1.611 ± 0.899 | 1.615 ± 1.147 | |
HNB | COII | 8 | 1(1), 8(1), 9(1), 11(1), 12(2), 13(1), 14(1) | 8 | 0.004 ± 0.002 | 2.314 ± 1.308 | 2.464 ± 1.692 |
Cytb | 12 | 1(3), 2(2), 4(1), 8(1), 10(1), 11(1), 12(1), 13(1), 14(1) | 13 | 0.006 ± 0.004 | 3.545 ± 1.655 | 2.231 ± 1.476 | |
JS | COII | 12 | 19(2), 20(10) | 1 | 0.000 ± 0.002 | 0.331 ± 0.331 | 0.303 ± 0.379 |
Cytb | 17 | 2(17) | 0 | 0.000 ± 0.000 | 0.000 ± 0.000 | 0.000 ± 0.000 | |
SC | COII | 18 | 6(3), 21(14), 22(1) | 2 | 0.001 ± 0.001 | 0.581 ± 0.435 | 0.477 ± 0.485 |
Cytb | 22 | 2(21), 4(1) | 1 | 0.000 ± 0.000 | 0.274 ± 0.274 | 0.091 ± 0.188 | |
GD | COII | 18 | 1(9), 23(1), 24(3), 25(1), 26(1), 27(1), 28(1), 29(1) | 7 | 0.002 ± 0.001 | 2.035 ± 1.006 | 1.288 ± 0.946 |
Cytb | 21 | 2(6), 4(2), 20(1), 21(2), 24(2), 26(1), 27(3), 28(1), 29(1), 30(1), 31(1) | 10 | 0.005 ± 0.003 | 2.780 ± 1.239 | 2.076 ± 1.350 | |
LN | COII | 24 | 1(4), 5(1), 7(1), 20(8), 30(1), 31(1), 32(3), 33(1), 34(1), 35(1), 36(1), 37(1) | 15 | 0.005 ± 0.002 | 4.285 ± 1.709 | 2.598 ± 1.606 |
Cytb | 27 | 2(14), 4(1), 32(1), 33(1), 34(1), 35(3), 36(1), 37(1), 38(2), 39(1), 40(1) | 9 | 0.005 ± 0.003 | 2.037 ± 0.928 | 1.926 ± 1.255 |
h is haplotype diversity, S is the number of segregating sites and θs and θπ are the estimates of nucleotide diversity. The bold haplotypes occur in more than one population and the number in parentheses indicates the frequency of the haplotype.