Publications des scientifiques de l'IRD

Karun A., Sajini K. K., Muralikrishna K. S., Rajesh M. K., Engelmann Florent. (2017). cryopreservation of arecanut (Areca catechu l.) pollen. Cryoletters, 38 (6), p. 463-470. ISSN 0143-2044.

Titre du document
cryopreservation of arecanut (Areca catechu l.) pollen
Année de publication
2017
Type de document
Article référencé dans le Web of Science WOS:000426409500006
Auteurs
Karun A., Sajini K. K., Muralikrishna K. S., Rajesh M. K., Engelmann Florent
Source
Cryoletters, 2017, 38 (6), p. 463-470 ISSN 0143-2044
BACKGROUND: Cryopreservation opens new avenues in the field of genetic resource conservation, especially in recalcitrant seeded palms such as arecanut for which field genebanks are exposed to pest and disease attacks and natural calamities. It is only through cryopreservation that the safety of the conserved germplasm can be assured at a relatively low cost for extended periods. OBJECTIVE: The objective of this work was to standardize various aspects of arecanut pollen cryopreservation, viz. collection and desiccation of pollen, in vitro germination, viability and fecundity studies. MATERIALS AND METHODS: Pollens of three arecanut genotypes (Sumangala, Hirehalli Dwarf and Hirehalli Dwarf x Sumangala) were collected in December 2013-February 2014. In vitro viability tests were conducted using fresh and desiccated pollen. Desiccated pollen was cryopreserved by direct immersion in liquid nitrogen and cryostored for different durations (24 hours to 2 years). Viability and fertility studies were conducted using cryopreserved pollen. RESULTS: Pollen extraction was achieved from fully opened male flowers by desiccation at room temperature (33-34 degrees C). A medium containing 2.5 g/L sucrose was found to be best for in vitro germination at room temperature. There was no significant difference in germination between desiccated and cryopreserved pollen whereas pollen tube length decreased significantly after cryopreservation. Fertility studies using HD x Sumangala pollen cryostored for various durations (1 month, 1 year and 2 years) showed the setting of 70, 43 and 62%, respectively. Normal nut set was observed using cryopreserved pollen. CONCLUSION: Pollen cryopreservation is a viable option for germplasm conservation and hybridization programmes in arecanut.
Plan de classement
Sciences du monde végétal [076] ; Biotechnologies [084]
Localisation
Fonds IRD [F B010072417]
Identifiant IRD
fdi:010072417
Contact