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   <subfield code="a">Micrografting of Protea cynaroides</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[H. Wu, E. du Toit, C. Reinhardt]</subfield>
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   <subfield code="a">The inability to induce rooting of in vitro-established Protea cynaroides microshoots has prevented the production of complete plantlets. A successful shoot-tip micrografting technique was developed using in vitro-germinated P. cynaroides seedlings as rootstocks and axenic microshoots established from pot plants as microscions. Thirty-day old seedlings, germinated on growth-regulator-free, half-strength Murashige and Skoog medium, were decapitated and a vertical incision made from the top end. The bottom ends of microshoots established on modified Murashige and Skoog medium were cut into a wedge (‘V') shape, and placed into the incision. The micrografted explants were cultured in a growth chamber with the temperature adjusted to 25±2°C, with a 12-h photoperiod. Best results were obtained by placing the microscions directly onto the rootstock without any pre-treatments. Dipping the explants in anti-oxidant solution or placing a layer of medium around the graft area led to the blackening of the microscion.</subfield>
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   <subfield code="a">Grafting</subfield>
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   <subfield code="a">King Protea</subfield>
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   <subfield code="a">Micropropagation</subfield>
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   <subfield code="a">EDTA : Ethylenediaminetetraacetate</subfield>
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   <subfield code="a">BAP : 6-Benzylaminopurine</subfield>
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   <subfield code="a">GA3 : Gibberellic acid</subfield>
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   <subfield code="a">PAR : Photosynthetic active radiation</subfield>
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   <subfield code="u">Department of Plant Production and Soil Science, Faculty of Natural and Agricultural Sciences, University of Pretoria, 0002, Pretoria, South Africa</subfield>
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   <subfield code="a">du Toit</subfield>
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