The present investigation focused to
revealed gene flow and genetic differentiation among riverine (Narmada river,
n=04), reservoir (Tighra reservoir, n=04 and hatchery raised (Fish Federation
Pond, n=07; Khatik Fish Farm, n=05) populations of Catla Catla (Hamilton,
1822) of Madhya Pradesh. Results clearly reflected as Riverine>Reservoir>Fish
Federation Pond>Khatik Fish Farm gene flow and even all parameter analyzed
for genetic divergence among the populations. Nei’s gene diversity (h) was
observed as 0.1382 in Fish Federation Pond, 0.1342 and 0.1739 in Khatik Fish
Farm and Narmada River, 0.1490 populations reflecting much higher gene
diversity in feral population. The Genetic Differentiation (GST) among the
populations was found as GST=0.2380, estimates of gene flow between population
(Nm=1.6010), intra-population heterozygosity as HS 0.2457 and total
heterozygosity as HT=0.3225 clearly reflecting less genetic differentiation as
overall when compared to other fish populations. Analyses genetic polymorphism
(P) as 38.59% in hatchery raised population was obtained which as well much
slighter as compared to wild populations since 60.30 in Narmada River and 51.63
in Tighra reservoir have been obtained. Overall research indicates that, as
compared to wild stock, the genetic changes including reduced genetic diversity
have taken place in hatched stocks. This baseline information on genetic
variation would be useful for planning intended for effective strategies for
conservation and remediation of Catla Catla freshwater fish species.
Freshwater animals
have been much greater losses than animals found in terrestrial ecosystems, and
freshwater fishes are among the world’s most endangered vertebrates. Most of
the fish used for human consumption is obtained through exploitation of wild
populations. Allelic diversity (richness) is one of the most important and
commonly used estimators of genetic diversity in populations. It strongly
depends on the effective population size and past evolutionary history.
However, the number of observed alleles and their frequency distribution also
depend on the sample size and the genetic marker system used. Thus, a practical
method for reliable estimation of genetic diversity parameters in large
populations is needed for population genetic studies and to develop
scientifically sound strategies for genetic resource conservation. RAPD
technique evaluates the genetic disparity within or between the taxa of concern
by assessing the occurrence or lack of each product, which is directed by
alteration in the DNA sequence at each locus.
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