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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Karuppusamy, S | - |
| dc.contributor.author | Aruna, V | - |
| dc.contributor.author | Kiranmai, C | - |
| dc.contributor.author | Pullaiah, T | - |
| dc.date.accessioned | 2009-07-23T11:07:27Z | - |
| dc.date.available | 2009-07-23T11:07:27Z | - |
| dc.date.issued | 2007-10 | - |
| dc.identifier.issn | 0975-0967 (Online); 0972-5849 (Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/5532 | - |
| dc.description | 541-544 | en_US |
| dc.description.abstract | A protocol for in vitro propagation of Hydrocotyle conferta Wight (Apiaceae) through axillary bud multiplication was established. Murashige and Skoog (MS) medium with 6.66 M N6-benzyladenine (BA) and 5.37 M -naphthalenacetic acid (NAA) was best suited for axillary bud multiplication including a mean of 21 shoots/node. Excision and culture of the nodal segments from the in vitro shoots on fresh medium with same concentrations of BA and NAA facilitated development of more than 25 shoots/node. Subsequent cultures enhanced the rate of shoot proliferation. The developed shoots rooted best on half strength MS medium with 0.54 M NAA. Plantlets established in pots exhibited 95% survival. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int. Cl.8 A01H4/00 | en_US |
| dc.source | IJBT Vol.6(4) [October 2007] | en_US |
| dc.subject | axillary bud multiplication | en_US |
| dc.subject | Hydrocotyle conferta | en_US |
| dc.subject | endemic umbellifer | en_US |
| dc.title | In vitro propagation of an endemic umbellifer, Hydrocotyle conferta | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJBT Vol.06(4) [October 2007] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJBT 6(4) 541-544.pdf | 266.13 kB | Adobe PDF | View/Open |
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M N6-benzyladenine (BA) and 5.37
-naphthalenacetic acid (NAA) was best suited for axillary bud multiplication including a mean of 21 shoots/node. Excision and culture of the nodal segments from the in vitro shoots on fresh medium with same concentrations of BA and NAA facilitated development of more than 25 shoots/node. Subsequent cultures enhanced the rate of shoot proliferation. The developed shoots rooted best on half strength MS medium with 0.54