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Table 3 Diversity indicators obtained from the nuclear SSR markers

From: High levels of gene flow and genetic diversity in Irish populations of Salix capreaL. inferred from chloroplast and nuclear SSR markers

Locus

N

Pred

Size

N A

N E

I

H O

H E

HW

F IS

F IT

F ST

G ST

D est

SB24

362

109-245

124-182

16

2.8

1.57

0.62

0.64

NS

−0.09NS

0.03

0.11**

0.05**

0.09**

SB38

364

105-161

106-156

15

9.0

2.34

0.86

0.89

NS

−0.09NS

0.03

0.11**

0.06**

0.33**

SB85

362

81-87

79-85

3

1.1

0.11

0.04

0.04

NS

−0.12NS

−0.02

0.09*

0.04*

0.002*

SB93

336

159-185

150-168

7

2.1

0.92

0.07

0.53

S

0.85NS

0.88

0.23*

0.12*

0.13*

SB194

362

105-152

108-130

11

5.9

1.95

0.75

0.83

S

−0.04NS

0.09

0.13**

0.07**

0.27**

SB199

212

102-140

98-126

8

2.4

1.20

0.10

0.58

S

0.71NS

0.79

0.28*

/

/

Mean1

333

  

10

3.9

1.35

0.41

0.58

 

0.08NS

0.30

0.16**

0.07**

0.10**

SE

24.6

  

2

1.2

0.32

0.15

0.12

      
  1. N = Sample Size, Pred = Predicted product size (bp) from Barker [10], Size = Allele size range (bp), N A  = No. of Obtained Alleles, N E  = No. of Effective Alleles, I = Shannon's Information Index, H O  = Observed Heterozygosity, H E  = Expected Heterozygosity, HW = exact test of Hardy-Weinberg equilibrium with a significance at p = 0.01, F IS  = Inbreeding coefficient within individuals in each subpopulation, F IT  = Inbreeding coefficient of an individual relative to the total population, F ST  = Genetic differentiation among populations, G ST  = Analog of F ST , D est  = Jost’s estimate of differentiation. 1Mean over loci rather than the arithmetic average, NSnon significant, *P < 0.05; **P < 0.001 Probability values are based on 999 permutations.