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Coconut (Cocos nucifera L.)
Coconut Plantlets from Leaf Tissue Culture
Scientific Name: cocos nucifera Linn. |
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Family: Palmaceae
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Origin |
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Comparatively little is known about the origin and early distribution
of the coconut palm, probably because it was so widely spread throughout
the tropical areas of the world so many years ago. It has variously
been thought to be native to the Malay Archipelago, the South Pacific
and tropical America.
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Distribution |
The coconut is widespread throughout the tropics, typically being found
along sandy shorelines. It has been spread largely by man but also by
natural means. The fruit can float for long distance and still germinate
to form new trees after being washed ashore. Commercial plantings are
confined to the tropical lowlands, but it will also fruit in a few warmer
subtropical areas.
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Uses |
The meat of immature coconuts can be eaten with a spoon or be scooped
out and made into ice cream. Coconut milk, abundant in unripe nuts,
is a refreshing and nutritious drink. The most important economic product
is obtained by drying the meat into copra which is pressed to produce
coconut oil, primarily used in making soap. Coconut oil is also used
for cooking and making margarine. The husk fiber is combed out and sold
as coir, a material for making rope and coconut matting. The trunks
may be used for building timbers and the leaves used for house thatching.
The coconut palm has little commercial importance in Florida but is
highly valued as an ornamental. It gives a tropical effect to the Florida
landscape and provides fruit for home use.
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Explants |
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Use the lower most 10cm segment of tender leaves, from two year
old nursery grown coconut seedlings as explant.
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Surface sterilize the tender leaf by dipping in 70% alcohol for
2-3 seconds.
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Cut the sterilized leaf into 5 mm long explants. The entire operation
is to be done in surface-sterilized (absolute alcohol) inoculation
hood (portable).
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Inoculate these explants on sterile culture medium
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Media & Culture conditions |
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Divide the media into 8 groups with a total of 22
sub groups. The 23 group stocks and 2 blanks: and prepare A1-3,B1-3,C1-3,D1-3,E1-5,F1-6,G
and H.
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Add agar and charcoal into all 2430 combinations after
adjusting the pH to5.8.
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Dispense the media in culture tubes and autoclave
it and check for contamination.
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All cultures should be incubated at 29 ± 1oC at a
photoperiod of 16 h light from white fluorescent lamps.
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Subculture every 4-5 weeks.Reduce the sucrose concentration
to 30g/l
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Plantlet
Regeneration |
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Observe the somatic embryogenesis with an incubation period of 16
weeks.
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Germinated embryos (with two leaves and primary root, almost four
months after inoculation) are transferred to liquid rooting medium.
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Subculture on -same medium every 4-5 weeks. Transfer to wide-mouth
and longer tubes whenever necessary.
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Plantlets with well-developed secondary and tertiary root and shoot
system (3-4 leaves, 20-25 cm height, 5-6 ml root volume) are ready
for transfer to small pots.
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Potting mixture consists of autoclave-sterilized soil: sand: decomposed
coir dust (1:1:1).
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Pre-treat the plantlets with Carbendazim (Ig/L) and IBA (1000 ppm)
for 1 hour each and transfer to the pots.
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Acclimatization |
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Cover the plantlets with polyethylene bags for 2-3 weeks and keep
them indoor at room temperature with artificial light.
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Supply Hoagland's solution once every 15 days.
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Irrigate to keep potting mixture moist.
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After three weeks, harden the plantlets by gradually perforating
the polyethylene bags and remove the bags at night for two weeks.
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After two weeks, remove the polythene bags completely and keep
plantlets indoor for one week.
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Transfer plantlets to bigger pots and keep them in net house with
50% shade.
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After 3-4 months, transfer the plantlets to big polythene bags containing
-soil and organic manure and keep them in a net house with 50% shade.
(Total duration from pot to polybag is 5-6 months). Irrigate regularly
and apply recommended dose of fertilizer whenever necessary.
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After 4-5 months, plantlets can be transferred to the field.
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Practical
Utility |
This protocol could be applied for rapid multiplication of elite genotype
and basic studies not only in coconut but also in other palms
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