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<records>
<record>
	<source-app name="Actavia">Actavia</source-app>
	<ref-type name="Journal Article">0</ref-type>
	<contributors>
		<authors>
			<author>Ogburia, M.N.</author>
		</authors>
		<secondary-authors></secondary-authors>
	</contributors>
	<titles><title>Somatic Embryogenesis, Plantlet Regeneration and Micropropagation of Cultivars and F&lt;sub&gt;1&lt;/sub&gt; Hybrids of Manihot esculenta</title></titles>
	<dates>
		<year>2003</year>
		<pub-dates><date>2003-11-1</date></pub-dates>
	</dates>
	<pages>429-432</pages>
	<abstract>Explants of four F&lt;sub&gt;1&lt;/sub&gt; hybrids (OMR 36-41/1, OMR 36-41/2, OMR 36-41/4 and OMR 36-41/5) and two cultivars (Rayong 1 and Rayong 60) of cassava (Manihot esculenta Crantz) were subjected to different combinations of 2,4-dichlorophenoxyacetic acid (2,4-D), 1-naphthaleneacetic acid (NAA), kinetin (KIN) and N&lt;sup&gt;6&lt;/sup&gt;-benzylaminopurine (BAP) to induce somatic embryogenesis, organogenesis and micropropagation. Shoot apices of the F&lt;sub&gt;1&lt;/sub&gt; hybrids exhibited higher frequency (62 - 74 %) of proliferation of somatic embryos than the cultivars (21 - 43 %) in Murashige and Skoog basal medium supplemented with 8 mg dm&lt;sup&gt;-3&lt;/sup&gt; 2,4-D and 0.5 mg dm&lt;sup&gt;-3&lt;/sup&gt; NAA. Nodal explants of regenerated plantlets were rapidly micropropagated with 90 % efficiency on a medium containing 0.1 mg dm&lt;sup&gt;-3&lt;/sup&gt; NAA and 0.05 mg dm&lt;sup&gt;-3&lt;/sup&gt; BAP irrespective of explant source.</abstract>
	<number>3</number>
	<volume>46</volume>
</record>
</records>
</xml>
