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   <subfield code="a">New basal media for half-anther culture of Anthurium andreanum Linden ex André cv. Tropical</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Budi Winarto, F. Rachmawati, Jaime Teixeira da Silva]</subfield>
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   <subfield code="a">A successful protocol for high frequency callus induction and plant regeneration from Anthurium andreanum Linden ex André cv. Tropical half-anthers is described. Different variables using Winarto and Teixeira and Murashige and Skoog basal media supplemented with several plant growth regulators [2,4-dichlorophenoxy acetic acid (0.1-1.0mg/l), α-naphthalene acetic acid (0.01-0.2mg/l), thidiazuron (0.5-2.0mg/l), 6-benzylaminopurine (0.5-1.0mg/l), and kinetin (0.5-1.0mg/l)] were tested for their ability to induce high frequency callusing in half-anthers, indirect regeneration and rooting of shoots. Basal medium, as well as the combination and concentration of hormones applied, had a significant effect on callus formation, shoot regeneration and adventitious root formation. Winarto and Teixeira-1, an original basal medium containing 0.01mg/l α-naphthalene acetic acid, 0.5mg/l thidiazuron and 1.0mg/l 6-benzylaminopurine was suitable for callus formation while an improved basal medium i.e., New Winarto-Teixeira-3 supplemented with 0.25mg/l 2,4-dichlorophenoxy acetic acid, 0.02mg/l α-naphthalene acetic acid, 1.5mg/l thidiazuron and 0.75mg/l 6-benzylaminopurine enhanced callus formation. High shoot regeneration and multiplication was also possible on New Winarto-Teixeira-3. Shoots formed a strong adventitious root system on New Winarto-Teixeira-3 containing 0.2mg/l α-naphthalene acetic acid and 1.0mg/l kinetin. Plantlets that varied in size and performance were successfully acclimatized and adapted to ex vitro conditions. Cytological analysis of 180 acclimatized-plantlets ex vitro revealed that 34 were haploid (n=14-18), 15 aneuploid (n=20-26), 126 diploid (n=28-34) and 5 triploid (n=45-57). The potential use of this protocol for developing half-anther culture of other Anthurium species or cultivars is discussed.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2011</subfield>
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   <subfield code="a">Basal medium</subfield>
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   <subfield code="a">Anther culture</subfield>
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   <subfield code="a">Anthurium andreanum</subfield>
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   <subfield code="a">Linden ex André cv. Tropical</subfield>
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   <subfield code="a">Tissue culture</subfield>
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   <subfield code="a">Acclimatization</subfield>
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   <subfield code="a">Winarto</subfield>
   <subfield code="D">Budi</subfield>
   <subfield code="u">Tissue Culture Laboratory, Indonesian Ornamental Crops Research Institute, Sindanglaya, P.O. Box 8, 43253, Pacet-Cianjur, West Java, Indonesia</subfield>
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   <subfield code="a">Rachmawati</subfield>
   <subfield code="D">F.</subfield>
   <subfield code="u">Tissue Culture Laboratory, Indonesian Ornamental Crops Research Institute, Sindanglaya, P.O. Box 8, 43253, Pacet-Cianjur, West Java, Indonesia</subfield>
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   <subfield code="a">Teixeira da Silva</subfield>
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   <subfield code="t">Plant Growth Regulation</subfield>
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   <subfield code="g">65/3(2011-12-01), 513-529</subfield>
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