<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">El Kbiach, Mohamed L'bachir</style></author><author><style face="normal" font="default" size="100%">Lamarti, Ahmed</style></author><author><style face="normal" font="default" size="100%">Abdali, Abdeslam</style></author><author><style face="normal" font="default" size="100%">Badoc, Alain</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Micropropagation du Chêne-liège (Quercus suber L.) par culture d'apex issus d'axes embryonnaires</style></title><secondary-title><style face="normal" font="default" size="100%">Acta Botanica Gallica</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">embryonic axis</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro culture</style></keyword><keyword><style  face="normal" font="default" size="100%">organogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2004</style></year></dates><publisher><style face="normal" font="default" size="100%">Taylor &amp; Francis</style></publisher><volume><style face="normal" font="default" size="100%">151</style></volume><pages><style face="normal" font="default" size="100%">401-413</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Abstract To improve the in vitro germination and development of cork oak embryonic axes, several mineral media were tested; Durzan medium modified 1/2 supplemented with 400 mg/l glutamine and 3% sucrose gave the best results. The action of BA alone or combined with other growth regulators was also studied. A low concentration (0.44 ?M) was found to give an acceptable percentage of plantlets. When combined with NAA, callogenesis was observed. The transfer of cultures in conditions of low luminosity led to the formation of several axillary buds. These buds were multiplied on a solid medium supplemented with GA3 at low concentration. The buds were elongated, then rooted on a growth regulator-free medium after brief dipping in an auxinic solution. The rooted plants were potted on horticultural substrate.</style></abstract><notes><style face="normal" font="default" size="100%">doi: 10.1080/12538078.2004.10515443</style></notes><research-notes><style face="normal" font="default" size="100%">doi: 10.1080/12538078.2004.10515443</style></research-notes></record></records></xml>