Table 2.
Results of initial polymorphic microsatellite marker screening in three populations of Tithonia diversifolia.
LC (N = 21) | YX (N = 17) | GX (N = 10) | ||||||||||
Locus | A | Ho | He | HWEa | A | Ho | He | HWEa | A | Ho | He | HWEa |
Cl3 | 3 | 0.286 | 0.643 | *** | 4 | 0.529 | 0.555 | *** | 2 | 0.600 | 0.480 | ns |
Cl12 | 2 | 0.350 | 0.489 | ns | 2 | 0.294 | 0.438 | ns | 2 | 0.300 | 0.255 | ns |
Cl23 | 2 | 0.286 | 0.444 | ns | 2 | 0.353 | 0.457 | ns | 2 | 0.500 | 0.375 | ns |
Cl28 | 2 | 0.333 | 0.459 | ns | 3 | 0.412 | 0.552 | *** | 2 | 0.200 | 0.480 | ns |
Cl42 | 2 | 0.095 | 0.363 | *** | 1 | 0.000 | 0.000 | — | 1 | 0.000 | 0.000 | — |
Cl52 | 2 | 0.143 | 0.459 | ** | 2 | 0.294 | 0.500 | ns | 2 | 0.500 | 0.495 | ns |
Cl53 | 3 | 0.143 | 0.541 | *** | 2 | 0.235 | 0.498 | * | 2 | 0.400 | 0.500 | ns |
Cl76 | 2 | 0.381 | 0.499 | ns | 3 | 0.235 | 0.443 | *** | 2 | 0.400 | 0.480 | ns |
Cl84 | 2 | 0.286 | 0.444 | ns | 2 | 0.353 | 0.498 | ns | 2 | 0.500 | 0.455 | ns |
Cl92 | 3 | 0.190 | 0.635 | *** | 2 | 0.059 | 0.251 | ** | 2 | 0.400 | 0.500 | ns |
Cl95 | 2 | 0.143 | 0.459 | ** | 2 | 0.059 | 0.493 | *** | 2 | 0.300 | 0.495 | ns |
Un1 | 2 | 0.667 | 0.444 | * | 2 | 0.824 | 0.484 | ** | 2 | 0.700 | 0.455 | ns |
Un5 | 2 | 0.190 | 0.499 | ** | 2 | 0.235 | 0.415 | ns | 2 | 0.300 | 0.495 | ns |
Un6 | 2 | 0.048 | 0.500 | *** | 2 | 0.438 | 0.482 | ns | 2 | 0.600 | 0.500 | ns |
Un21 | 2 | 0.286 | 0.472 | ns | 2 | 0.235 | 0.484 | * | 2 | 0.200 | 0.320 | ns |
Un23 | 2 | 0.476 | 0.472 | ns | 2 | 0.706 | 0.498 | ns | 2 | 0.700 | 0.495 | ns |
Note: A = number of alleles; He = expected heterozygosity; Ho = observed heterozygosity; HWE = Hardy–Weinberg equilibrium; N = sample size.
Deviations from HWE at *P < 0.05, **P < 0.01, ***P < 0.001; ns = not significant.