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. 2017 Sep 26;67(2):255–264. doi: 10.1111/ppa.12762

Table 2.

Genotypic diversity, linkage disequilibrium, frequency of MAT1‐1 and presence of HfMV1 ssRNA virus for Hymenoscyphus fraxineus sampled from three established (−E) or mixed (−M) locations and three planted (−P) locations

Subpopulationa N H No. of monomorphic SNP markers H S d P ( d) MAT1‐1 % (P χ2) HfMV1 % (no. tested)
EPW‐E 19 2.94 3 0.354 −0.0052 0.97 32 (0.3) 67 (15)
LWD‐E 13 2.56 6 0.309 0.0130 0.14 54 (0.8) 20 (10)
PND‐M 14 2.64 0 0.451 0.0523 <0.001 71 (0.3) 100 (13)
BWY‐P 10 2.30 3 0.365 0.0098 0.14 80 (0.2) 46 (13)
ISC‐P 14 2.64 7 0.343 0.0311 0.14 36 (0.5) 87 (15)
PTW‐P 20 3.00 5 0.294 0.0107 0.64 40 (0.5) 67 (24)
Total 90 4.50 0.411 0.0206 <0.001 49 (0.9) 67; = 0.0007

28 SNP markers were tested on each population.

N, sample size; H, Shannon–Wiener index; H S, Nei's gene diversity (expected heterozygosity); d, standardized index of multilocus linkage disequilibrium (Agapow & Burt, 2001); P, value for significance of d. The MAT1‐1 allele frequencies at each site were tested for deviation from a 1:1 ratio using a χ2 test with 1 degree of freedom. Homogeneity of the frequency of HfMV1 across sites was tested by a χ2 test (5 d.f.).

a

For details of subpopulations see Table S1.