Tissue Culture Technology in Arecanut

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TISSUE CULTURE TECHNOLOGY

IN ARECANUT
PRESENTED BY
. SASIRA.D, 2018006039
NEED FOR TISSUE CULTURE
TECHNOLOGY IN ARECANUT
• Mass multiplication of dwarf arecanut.
( variety – Hirehalli) and it’s hybrids

• One of the major production constraints of


arecanut – devastating yellow leaf disease
( YCD).
YELLOW LEAF DISEASE. DWARF
HYBRIDS
Tissue culture seems to be the
only vegetative propagation
tool applicable to areca palm.
TISSUE CULTURE PROTOCOL AT CPCRI:

• Arecanut tissue culture protocol – standardized by


CPCRI, Kasaragod.
• Through Inflorescence explant.
• For rapid multiplication of genotypes such as
* Yellow Leaf Disease ( YCD) resistant palms.
* Dwarf hybrids development.
ESTABLISHMENT OF PROTOCOL

• More than 60 arecanut palms propagated


using this protocol, planted in different
locations.
• Their growth and reproduction are similar
to seed – borne plants.
FUTURE THRUST AREAS OF PALM:

• Strengthening of germplasm collection and characterization of


different traits for utilization in breeding programmes
• Cryopreservation of germplasm and development of molecular
markers for marker assisted selection (MAS) in
breedingprogrammes.
• Development of regeneration protocol.
FUTURE THRUST AREAS OF PALM:

• Development of theoretical ideotype forfocused crop


improvement
• Understanding the abiotic stress tolerance and screening
germplasm for tolerance to different stresses.
• Development of integrated eco friendly crop protection
PROTOCOL FOR IN VITRO
PROPAGATION IN
ARECANUT
MEDIA REQUIREMENTS FOR GROWTH:

• M.S media, White media, Branton and Blake’s (BB) media were used.
• GROWTH REGULATORS ; Auxin + Giberellins, 2,4-D were used.
• Darkening effect of activated charcoal – induced
rooting in shoot cultures.
• Synergistic action of abscissic acid and auxin –
enhanced the frequency of rooting.
OBSERVATIONS AND RESULTS:

Within 4 weeks,
• Greenish soft callus formed.
• 90% of shoots formed after 4 weeks.
After 7-8 weeks
• Darkness wounded regions of explants
. Formed callus with yellow soft, glutinous structures
OBSERVATIONS AND RESULTS:

• The embryos developed into plantlets after 10weeks


of culture on basal medium free of plantgrowth
regulators.
• After subculturing everymonth for three months the
plantlets weretransferred to containers for
acclimatization inthe green house.
• The survival rate was 24 %.
REFERENCE WEBSITES :

1. agritech.tnau.ac.in
2. https://icar.org.in
3. www.researchgate.net
THANK YOU
FOR
YOUR PATIENCE !

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