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   <subfield code="a">In Vitro Propagation Of Four Watsonia Species</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Glendon Ascough, John Erwin, Johannes van Staden]</subfield>
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   <subfield code="a">The genus Watsonia has a number of species with potential to be developed as new ornamental crop plants, but to date there are no reports on in vitro propagation of any member of this genus. Seeds from four Watsonia species, Watsonia gladioloides, Watsonia lepida, Watsonia laccata, and Watsonia vanderspuyiae were decontaminated and germinated on one-tenth strength MS media without hormones or sucrose. Shoots were induced from seedling hypocotyl segments when both an auxin [α-naphthaleneacetic acid (NAA)] and cytokinin [N6−benzylaminopurine (BA)] were present in the medium, while root and leaf explants failed to produce shoots. Multiplication of axillary shoots was greatest when only BA (0.5mgl−1) was added to the medium. Shoot explants propagated in a ‘liquid-shake' culture exhibited greater growth rates than those on agar-solidified medium, but shoot production varied between species. Meristemoids were induced in all species, but no significant trend was found between growth index (GI) and meristemoid formation, suggesting that reduction in GI may not necessarily be a prerequisite for producing meristemoids. Corm formation was inconsistent and storage organs could only be induced in one of the four species, W. vanderspuyiae. This occurred best at 25°C with 3% sucrose and an agar level of 15%. Indole-3-acetic acid (IAA) and NAA at 1mgl−1 significantly increased mean number of roots per shoot explant on all four species, while indole-3-butyric acid (IBA) was more effective when applied at 0.1mgl−1. Plantlet survival ex vitro was negatively affected when NAA and 2,4-dichlorophenoxyacetic acid (2,4-D) were used to root shoot explants for all species. In W. laccata, all auxin treatments [IAA, IBA, NAA, phenylacetic acid (PAA), and 2,4-D] at a concentration of 1mgl−1 significantly reduced ex vitro survival of plantlets. Successful micropropagation of Watsonia is an important step in the further development of this genus as a horticultural crop.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2006</subfield>
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   <subfield code="a">Acclimatization</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Corm formation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Iridaceae</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Liquid culture</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">rooting</subfield>
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   <subfield code="a">2,4-D : 2,4-dichlorophenoxyacetic acid</subfield>
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   <subfield code="a">AC : activated charcoal</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">ANOVA : analysis of variance</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">BA : N6-benzylaminopurine</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">GI : growth index</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">IAA : indole-3-acetic acid</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">IBA : indol-3-butyric acid</subfield>
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   <subfield code="a">MS : Murashige and Skoog basal medium</subfield>
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   <subfield code="a">NAA : α-naphthaleneacetic acid</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">PAA : phenylacetic acid</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">PP3 : paclobutrazol</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Ascough</subfield>
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   <subfield code="a">Erwin</subfield>
   <subfield code="D">John</subfield>
   <subfield code="u">Department of Horticultural Science, University of Minnesota, 1970 Folwell Ave., 55108, St Paul, MN, USA</subfield>
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   <subfield code="a">van Staden</subfield>
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   <subfield code="u">Research Centre for Plant Growth and Development, School of Biological and Conservation Sciences, University of KwaZulu-Natal, Private Bag X01, 3209, Pietermaritzburg, Scottsville, South Africa</subfield>
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   <subfield code="t">Plant Cell, Tissue and Organ Culture</subfield>
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   <subfield code="g">88/2(2007-02-01), 135-145</subfield>
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