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Micropropagation of Carnation
(Englisch)
An efficient multiplication protocol
Ajitabh Bora & Madhumita C Talukdar

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Autor/Autorin: Bora Ajitabh

Ajitabh Bora, born in 1981, did his post graduation from Assam Agricultural University, Jorhat, Assam. He initially joined ICAR as Asstt. Farm Manager and is presently working as Scientist `B´ at Defence Research Laboratory, Tezpur, Assam. He has several papers in national and international journals to his credit.

Autor/Autorin: C Talukdar Madhumita

Ajitabh Bora, born in 1981, did his post graduation from Assam Agricultural University, Jorhat, Assam. He initially joined ICAR as Asstt. Farm Manager and is presently working as Scientist `B´ at Defence Research Laboratory, Tezpur, Assam. He has several papers in national and international journals to his credit.
Carnations are commercially propagated in large scale through tissue culture. The present investigation was undertaken to optimize an efficient in vitro propagation method for three carnation cultivars viz. Malaga, Empire and Lipstick. The optimal medium for multiple-shoot proliferation from shoot-tip of cv. Malaga was found to be MS medium supplemented with 0.5 mg L-1 NAA, 0.5 mgL-1 Kinetin and 0.5 mg L-1 GA3, while in case of cv. Empire it was MS medium supplemented with 0.1 mg L-1 NAA, 0.75 mg L-1 BAP and 0.5 mg L-1 GA3 and in cv. Lipstick it was MS medium supplemented with 0.5 mg L-1 NAA, 1.5 mg L-1 Kinetin and 0.5 mg L-1 GA3 respectively. The optimal medium for multiple-shoot proliferation from nodal segment of the in vitro raised shoots was found to be MS medium supplemented with 0.5 mg L-1 NAA, 0.5 mg L-1 Kinetin and 0.5 mg L-1 GA3 for all the cultivars under study. Rooting from the in vitro raised individual shoots of the three cultivars was found to be best in MS medium supplemented with 0.5 mg L-1 IBA. High survival percentage of 90 per cent was recorded in the substrate vermiculite in all the three cultivars.
Carnations are commercially propagated in large scale through tissue culture. The present investigation was undertaken to optimize an efficient in vitro propagation method for three carnation cultivars viz. Malaga, Empire and Lipstick. The optimal medium for multiple-shoot proliferation from shoot-tip of cv. Malaga was found to be MS medium supplemented with 0.5 mg L-1 NAA, 0.5 mgL-1 Kinetin and 0.5 mg L-1 GA3, while in case of cv. Empire it was MS medium supplemented with 0.1 mg L-1 NAA, 0.75 mg L-1 BAP and 0.5 mg L-1 GA3 and in cv. Lipstick it was MS medium supplemented with 0.5 mg L-1 NAA, 1.5 mg L-1 Kinetin and 0.5 mg L-1 GA3 respectively. The optimal medium for multiple-shoot proliferation from nodal segment of the in vitro raised shoots was found to be MS medium supplemented with 0.5 mg L-1 NAA, 0.5 mg L-1 Kinetin and 0.5 mg L-1 GA3 for all the cultivars under study. Rooting from the in vitro raised individual shoots of the three cultivars was found to be best in MS medium supplemented with 0.5 mg L-1 IBA. High survival percentage of 90 per cent was recorded in the substrate vermiculite in all the three cultivars.

Über den Autor



Ajitabh Bora, nascido em 1981, fez a sua pós graduação na Universidade Agrícola de Assam, Jorhat, Assam. Inicialmente ingressou na ICAR como Asstt. Director Agrícola e trabalha actualmente como Cientista 'B' no Laboratório de Investigação em Defesa, Tezpur, Assam. Tem vários artigos em revistas nacionais e internacionais em seu crédito.


Klappentext

Carnations are commercially propagated in large scale through tissue culture. The present investigation was undertaken to optimize an efficient in vitro propagation method for three carnation cultivars viz. Malaga, Empire and Lipstick. The optimal medium for multiple-shoot proliferation from shoot-tip of cv. Malaga was found to be MS medium supplemented with 0.5 mg L-1 NAA, 0.5 mgL-1 Kinetin and 0.5 mg L-1 GA3, while in case of cv. Empire it was MS medium supplemented with 0.1 mg L-1 NAA, 0.75 mg L-1 BAP and 0.5 mg L-1 GA3 and in cv. Lipstick it was MS medium supplemented with 0.5 mg L-1 NAA, 1.5 mg L-1 Kinetin and 0.5 mg L-1 GA3 respectively. The optimal medium for multiple-shoot proliferation from nodal segment of the in vitro raised shoots was found to be MS medium supplemented with 0.5 mg L-1 NAA, 0.5 mg L-1 Kinetin and 0.5 mg L-1 GA3 for all the cultivars under study. Rooting from the in vitro raised individual shoots of the three cultivars was found to be best in MS medium supplemented with 0.5 mg L-1 IBA. High survival percentage of 90 per cent was recorded in the substrate vermiculite in all the three cultivars.



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