

H E A L T H Y P L A N T S A N D M IC R O P R O P A G A T IO N
EFFECTOF
I
NVITRO
LONG-TERMSHOOTMULTIPLICATIONFOR
MASSCLONALPROPAGATIONOFBIRCHANDPOPLAR
O.S.Mashkina, T.M.Tabatskaya, L.M.Starodubtseva
Research Institute o fForest Genetics and Breeding, Russia, 394043, Voronezh,
Lomonosov str., 105. E-Mail:
ilgis@lesgen.voronezh.suUsing o f tissue culture methods opens great prospects for mass
reproduction and preservation of a valuable gene pool of broad-leaved woody
species.
We studied a regeneration capacity of
in vitro
long-term cultivated
Karelian birch with patterned wood and five productive triploid forms of P.
alba and P. canescens which are dif-ficult for propagation by traditional
methods. Plant regeneration from stem (in birch) and nodal (in poplar)
explants of adult trees was performed using our original technology (Butova,
Tabatskaya, Skrobova, 1990; Mashkina, 1995). Long-term (during 4-6 years)
repeated (once per 6 months) shoot multiplication was carried out on Boulay
(1980) medium without hormones for birch and on halfstrength MS medium
( Murashige and Skoog, 1962) for poplar
The possibility of
in vitro
all-the year-round micropropagation of birch
(during 6 years) and poplar (during 4 years) without aging symptoms and
loss of regeneration capacity is shown. The optimal duration for one cycle of
shoot multiplication of plantlets was found to be 2-3 months. During this
period each plantlet gives 4-5 nodal segments with one axillary bud in birch
and 6-10 ones in poplar. After one year (4-6 cycles of shoot multiplication) it
is possible to obtain up to 500 thousand or one million microshoots of birch
and poplar, respectively. The sprouts of long-term shoot multiplication were
characterized by good growth and high rhizogenesis
in vitro
, regardless of
the season. Plantlets showed high survival rate and adaptation to changeable
environments: laboratory, greenhouse, field. Seedlings were homogenous
on morphological properties.
Thus,
in vitro
long term shoot multiplication is one of the ways to simplify
and to intensify the clonal propagation of adult birch and poplar trees. The
method described excludes the laborious and prolonged season-dependent
initial stage of annual explantation and renewal of the starting cultures.
Besides, multiplication coefficient increases due to a ll-the year-round
propagation of plantlets and mass yield of seedlings. Rare subcultivation
(once per 6 months) with the preservation of plant regeneration gives a
possibility to keep
in vitro
the valuable genetic material of the forest tree
species and to maintain the juvenile of adult initial genotypes.
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