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DC Field | Value | Language |
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dc.contributor.author | Seran, T.H. | |
dc.contributor.author | Hirimburegama, Kshanika | |
dc.contributor.author | Hirimburegama, W.K. | |
dc.contributor.author | Shanmugarajah, V. | |
dc.date.accessioned | 2012-05-15T03:50:47Z | |
dc.date.available | 2012-05-15T03:50:47Z | |
dc.date.issued | 1999 | |
dc.identifier.citation | Journal of National Science Foundation Sri Lanka 1999 27l3i. | en_US |
dc.identifier.uri | http://archive.cmb.ac.lk:8080/xmlui/handle/70130/2473 | - |
dc.description.abstract | This study was carried out to regenerate haploids from cultured anthers of lea clones. M o r p h o l o g i c a l and histological studies on t h e a n t h e r callus development revealed that nuclei of numerous microspores began to d i v i d e unequally, forming multicellular structures during the first week of culture and anther lobes swelled gradually until bursting. The rate of callus induction was rapid d u r i n g fi-10 weeks and compact greenish c a l l i were formed from anthers. C a l l i hecamc more heterogeneous with time in culture. The determination of ploidy levels in anther callus showed that two levels of ploidy were present i n callus. In the callus, the percentage of haploid cells was more (68%) than that of diploid (6%). The study on comparison of callus growth i n anthers of different clones indicated that the survival of anthers of three clones TRI 2043, T R I 2023 and TRI 2025 was high (highest was 98%, the lowest.78%) and calli were produced in anthers of all clones used i n this t r i a l . TRI 2043 exhibited relatively more callus formation (76.2 mg) from anther c u l t u r e d i n half M u r a s h i g e and Skoog (MS) medium - w i t h 2,4 D a nd B A P grown in l i g h t , followed by T R I 2023, T R I 2024, TRI 2025 and TRI 777. In the dark, significant callus growth was observed in four clones (TRI 2025, TRI 2024, TRI 2023 and TRI 777). Calli that formed in light turned dark green, meristemoid like structures after transfer to the same medium without 2,4 D. However, plantlcts could not be regenerated. | |
dc.language.iso | en | en_US |
dc.title | Callus formation in anther culture of tea clones, camellia sinensis (l.) O.kuntze | en_US |
dc.type | Journal abstract | en_US |
Appears in Collections: | Department of Plant Sciences |
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2-1-1-14.pdf | 41.12 kB | Adobe PDF | View/Open |
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