The current investigation reports the evaluation and identification of gene
tic diversity in P. ciliata using the RAPD assay. Eighteen random decamer p
rimers were used to assess variation within twenty five different clones, r
epresenting various provenances fi om the Himalayan region. A total of 159
amplification produces were obtained of which 111 were polymorphic while th
e remaining were monomorphic in nature, informative primers producing high
multiplex ratio were identified from the study The potential utility of the
se primers for large scale screening of germplasm and designing conservatio
n strategies in the species has been discussed. The JACCARD'S similarity co
efficient and the UPGMA clustering method were employed to construct the ph
ylogenetic tree. The dendrogram revealed a high level of variation between
the clones which was found to lie in accordance to the diversity observed u
sing morphological data. Two distinct clusters namely C1 and C2 were identi
fied.
The cluster C1 comprised of twenty three of the twenty five accessions and
was thus designated to be the major cluster while C2 consisted of only two
clones and was thus considered to be a minor cluster: The major cluster CI
was comprised of distinct sub-clusters which were found to be in concordanc
e to their geographical distribution. Highest Similarity within the major c
luster was detected between the clones Katrain and Karain Bihal while the c
lone Lidder was found to be the most distinct. Bootstrap analysis and princ
ipal coordinate (PCO) analysis was performed which supported the pattern of
clustering in the dendrogram. The clustering of the other clones in relati
on to their geographical location has been discussed.