GENETIC VARIABILITY AND DIFFERENTIATION ... - ePrints@USM
GENETIC VARIABILITY AND DIFFERENTIATION ... - ePrints@USM
GENETIC VARIABILITY AND DIFFERENTIATION ... - ePrints@USM
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LIST OF TABLES<br />
Table 2.1 Methods available for genetically characterizing<br />
individuals and populations and their applicability to each<br />
issue. Techniques with + can be used for the purpose<br />
specified, with several + indicating the technique has high<br />
utility, ? are cases where the technique is useful in only<br />
some cases, while – indicates that the technique is not<br />
useful in this context (Adapted from Frankham et al.,<br />
2002).<br />
Table 2.2 Some commonly applied molecular marker systems to<br />
detect differences among closely related populations<br />
(Adapted from O’Connell and Wright, 1997).<br />
Table 3.1 Sampling site, sample type, sample size and date of<br />
capture of Lates calcarifer.<br />
Table 3.2 List of 13 microsatellite loci used in this study. 35<br />
Table 3.3 Solutions and concentration used for the preparation of 6<br />
% non-denaturing polyacrylmide gel.<br />
Table 4.1 Summary of annealing temperature (Tm), concentration of<br />
MgCl2, size range (bp) of the alleles and number of alleles<br />
for each locus screened.<br />
Table 4.2 Detection of null allele, stutter bands and the probability<br />
(P) of deviations from Hardy-Weinberg Equilibrium in<br />
each locus for each population.<br />
Table 4.3 Allelic variability at ten microsatellite loci in Lates<br />
calcarifer.<br />
Table 4.4 Pairwise FST values for Asian sea bass feral and cultured<br />
populations sampled in Malaysia.<br />
Table 4.5 Proportion of membership (Q) of each L. calcarifer<br />
population in each of the five genetic clusters which<br />
identified by STRUCTURE. The major proportion<br />
membership of cluster in a population was indicated with<br />
bold values.<br />
Table 4.6 The table gives the probability that the observed<br />
heterozygosity is larger than the average hetrozygosity<br />
calculated by BOTTLENECK program under the Infinite<br />
allele model (IAM), Stepwise mutation model, (SMM)<br />
and Two-phase model, TPM (95% Single-step mutations,<br />
5% Multiple-step mutations) and allele frequencies<br />
distribution mode for each population.<br />
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