<?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%">Liñán, Juana</style></author><author><style face="normal" font="default" size="100%">Cantos, Manuel</style></author><author><style face="normal" font="default" size="100%">Troncoso, Javier</style></author><author><style face="normal" font="default" size="100%">García, José L.</style></author><author><style face="normal" font="default" size="100%">Fernández, Antonio</style></author><author><style face="normal" font="default" size="100%">Troncoso, Antonio</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Some propagation methods for cloning holm oak (Quercus ilex L.) plants</style></title><secondary-title><style face="normal" font="default" size="100%">Central European Journal of Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Holm oak</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">rooting</style></keyword><keyword><style  face="normal" font="default" size="100%">seed germination</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2011///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/10.2478/s11535-011-0007-y</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">359 - 364</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Holm oak (Quercus ilex L.), a typical evergreen tree of the Mediterranean area, is very important due to its ecological and economical values. Propagation of this species is extremely difficult and traditionally carried out only by seed germination. In this work, mature acorns were germinated in vitro and in peat substrate in aseptic and non-aseptic conditions. Explants from the seedlings obtained were propagated in vitro in WPM plus 4 µM BA. Plant regeneration was achieved from hypocotyls and root segments cultured in vitro on modified Gamborg medium plus 20 µM BA and 20 µM NAA. 13.8% of the hypocotyls and approximately 30% of the root segments developed both shoots and roots after 30 days of culture. Rooting of stem segments was obtained both in vitro and ex vitro by basal dipping in IBA solutions. Within ex vitro rooting, mother plant age had major influence on the percentage of rooting of the cuttings as the younger plants showed higher ability to root. In this way, Q. ilex plants could be propagated and cloned. The procedure described here would be a very useful tool for breeding programs since vegetative propagation of selected individuals can be achieved.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><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%">Liñán, Juana</style></author><author><style face="normal" font="default" size="100%">Cantos, Manuel</style></author><author><style face="normal" font="default" size="100%">Troncoso, Javier</style></author><author><style face="normal" font="default" size="100%">García, José L</style></author><author><style face="normal" font="default" size="100%">Fernández, Antonio</style></author><author><style face="normal" font="default" size="100%">Troncoso, Antonio</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Some propagation methods for cloning holm oak (Quercus ilex L.) plants</style></title><secondary-title><style face="normal" font="default" size="100%">Central European Journal of Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Holm oak</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">rooting</style></keyword><keyword><style  face="normal" font="default" size="100%">seed germination</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">359-364</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Holm oak (Quercus ilex L.), a typical evergreen tree of the Mediterranean area, is very important due to its ecological and economical values. Propagation of this species is extremely difficult and traditionally carried out only by seed germination. In this work, mature acorns were germinated in vitro and in peat substrate in aseptic and non-aseptic conditions. Explants from the seedlings obtained were propagated in vitro in WPM plus 4 µM BA. Plant regeneration was achieved from hypocotyls and root segments cultured in vitro on modified Gamborg medium plus 20 µM BA and 20 µM NAA. 13.8% of the hypocotyls and approximately 30% of the root segments developed both shoots and roots after 30 days of culture. Rooting of stem segments was obtained both in vitro and ex vitro by basal dipping in IBA solutions. Within ex vitro rooting, mother plant age had major influence on the percentage of rooting of the cuttings as the younger plants showed higher ability to root. In this way, Q. ilex plants could be propagated and cloned. The procedure described here would be a very useful tool for breeding programs since vegetative propagation of selected individuals can be achieved.</style></abstract></record><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%">Díaz-Delgado, R.</style></author><author><style face="normal" font="default" size="100%">Lloret, F.</style></author><author><style face="normal" font="default" size="100%">Pons, X.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of fire severity on plant regeneration by means of remote sensing imagery</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Remote Sensing</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">dominant species (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">fire severity</style></keyword><keyword><style  face="normal" font="default" size="100%">NDVI</style></keyword><keyword><style  face="normal" font="default" size="100%">plant damage</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2003///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1080/01431160210144732</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">24</style></volume><pages><style face="normal" font="default" size="100%">1751 - 1763</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In this paper we analyse the interactions between fire severity (plant damage) and plant regeneration after fire by means of remote sensing imagery and a field fire severity map. A severity map was constructed over a large fire (2692 ha) occurring in July 1994 in the Barcelona province (north-east of Spain). Seven severity classes were assigned to the apparent plant damage as a function of burning intensity. Several Landsat TM and MSS images from dates immediately before and after the fire were employed to monitor plant regeneration processes as well as to evaluate the relationship with fire severity observed in situ . Plant regeneration was monitored using NDVI measurements (average class values standardized with neighbour unburned control plots). Pre-fire NDVI measurements were extracted for every plant cover category (7), field fire severity class (7), and spatial cross-tabulation of both layers (33) and compared to post-fire values. NDVI decline due to fire was positively correlated with field fire severity class. Results show different patterns of recovery for each dominant species, severity class and combination of both factors. For all cases a significant negative correlation was found between damage and regeneration ability. This work leads to a better understanding of the influence of severity, a major fire regime parameter on plant regeneration, and may aid to manage restoration on areas burned under different fire severity levels.</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1080/01431160210144732doi: 10.1080/01431160210144732The following values have no corresponding Zotero field:&lt;br/&gt;publisher: Taylor &amp; Francis</style></notes></record><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%">Díaz-Delgado, R</style></author><author><style face="normal" font="default" size="100%">Lloret, F</style></author><author><style face="normal" font="default" size="100%">Pons, X</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of fire severity on plant regeneration by means of remote sensing imagery</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Remote Sensing</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">dominant species (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">fire severity</style></keyword><keyword><style  face="normal" font="default" size="100%">NDVI</style></keyword><keyword><style  face="normal" font="default" size="100%">plant damage</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year></dates><publisher><style face="normal" font="default" size="100%">Taylor &amp; Francis</style></publisher><volume><style face="normal" font="default" size="100%">24</style></volume><pages><style face="normal" font="default" size="100%">1751-1763</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In this paper we analyse the interactions between fire severity (plant damage) and plant regeneration after fire by means of remote sensing imagery and a field fire severity map. A severity map was constructed over a large fire (2692 ha) occurring in July 1994 in the Barcelona province (north-east of Spain). Seven severity classes were assigned to the apparent plant damage as a function of burning intensity. Several Landsat TM and MSS images from dates immediately before and after the fire were employed to monitor plant regeneration processes as well as to evaluate the relationship with fire severity observed in situ . Plant regeneration was monitored using NDVI measurements (average class values standardized with neighbour unburned control plots). Pre-fire NDVI measurements were extracted for every plant cover category (7), field fire severity class (7), and spatial cross-tabulation of both layers (33) and compared to post-fire values. NDVI decline due to fire was positively correlated with field fire severity class. Results show different patterns of recovery for each dominant species, severity class and combination of both factors. For all cases a significant negative correlation was found between damage and regeneration ability. This work leads to a better understanding of the influence of severity, a major fire regime parameter on plant regeneration, and may aid to manage restoration on areas burned under different fire severity levels.</style></abstract><notes><style face="normal" font="default" size="100%">doi: 10.1080/01431160210144732</style></notes><research-notes><style face="normal" font="default" size="100%">doi: 10.1080/01431160210144732</style></research-notes></record><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%">Fernández-Guijarro, Bárbara</style></author><author><style face="normal" font="default" size="100%">Celestino, Cristina</style></author><author><style face="normal" font="default" size="100%">Toribio, Mariano</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of external factors on secondary embryogenesis and germination in somatic embryos from leaves of Quercus suber</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Cell, Tissue and Organ Culture</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%">culture media</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">recurrent embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">repetitive embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1995</style></year></dates><volume><style face="normal" font="default" size="100%">41</style></volume><pages><style face="normal" font="default" size="100%">99-106</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Somatic embryogenesis was obtained in cultures of leaves from young seedlings of Quercus suber L. A two- stage process, in which benzyladenine and naphthaleneacetic acid were added first at high and then at low concentrations, was required to initiate the process. Somatic embryos arose when the explants were subsequently placed on medium lacking plant growth regulators. The embryogenic lines remained productive, by means of secondary embryogenesis, on medium without growth regulators. However, this repetitive induction was influenced by the macronutrient composition of the culture medium. Both low total nitrogen content and high reduced nitrogen concentration decreased the percentage of somatic embryos that showed secondary embryogenesis. Our results suggest that alternate culture on medium that increases embryo proliferation and a low salt medium prohibiting embryo formation will partially synchronize embryo development. Chilling slightly reduced secondary embryogenesis but gave a modest increase in germination. Maturation under light followed by storage at 4 °C for at least 30 days gave the best results in switching embryos from an embryogenic pathway to a germinative one. Under these conditions 15% of embryos showed coordinated root and shoot growth and 35% formed either shoots or mostly roots. These percentages were higher than those of embryos matured in darkness. This result indicates that a specific treatment is required after maturation and before chilling to activate the switch from secondary embryo formation to germination.</style></abstract></record><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%">Fernández-Guijarro, Bárbara</style></author><author><style face="normal" font="default" size="100%">Celestino, Cristina</style></author><author><style face="normal" font="default" size="100%">Toribio, Mariano</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of external factors on secondary embryogenesis and germination in somatic embryos from leaves of Quercus suber</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Cell, Tissue and Organ Culture</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%">culture media</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">recurrent embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">repetitive embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1995</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1995///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/10.1007/BF00051578</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">41</style></volume><pages><style face="normal" font="default" size="100%">99 - 106</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Somatic embryogenesis was obtained in cultures of leaves from young seedlings of Quercus suber L. A two- stage process, in which benzyladenine and naphthaleneacetic acid were added first at high and then at low concentrations, was required to initiate the process. Somatic embryos arose when the explants were subsequently placed on medium lacking plant growth regulators. The embryogenic lines remained productive, by means of secondary embryogenesis, on medium without growth regulators. However, this repetitive induction was influenced by the macronutrient composition of the culture medium. Both low total nitrogen content and high reduced nitrogen concentration decreased the percentage of somatic embryos that showed secondary embryogenesis. Our results suggest that alternate culture on medium that increases embryo proliferation and a low salt medium prohibiting embryo formation will partially synchronize embryo development. Chilling slightly reduced secondary embryogenesis but gave a modest increase in germination. Maturation under light followed by storage at 4 °C for at least 30 days gave the best results in switching embryos from an embryogenic pathway to a germinative one. Under these conditions 15% of embryos showed coordinated root and shoot growth and 35% formed either shoots or mostly roots. These percentages were higher than those of embryos matured in darkness. This result indicates that a specific treatment is required after maturation and before chilling to activate the switch from secondary embryo formation to germination.</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>3</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fernández Guijarro, B</style></author><author><style face="normal" font="default" size="100%">CELESTINO, C</style></author><author><style face="normal" font="default" size="100%">TORIBIO, M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">OBTENCION DE PLANTAS A PARTIR DE EMBRIONES SOMATICOS DE QUERCUS SUBER L</style></title><secondary-title><style face="normal" font="default" size="100%">Congreso Forestal Español, Lourizán - Pontevedra. 1993</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">adventive embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">culture media</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">secondary embryogenesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1993</style></year></dates><pages><style face="normal" font="default" size="100%">337-341</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">This paper gives a procedure to regenerate plants of cork oak through somatic embryogenesis. The somatic embryos were obtained in leaves from young seedlings and cotyledonary fragments from mature acorns of cork oak. The explants were cultured in three stage process in wich BA and NAA concentration were decreasing. Different methods were used to germinate the embryos. Dessication and culture in low salt concentration medium were chosen to give the best results</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fernández Guijarro, B.</style></author><author><style face="normal" font="default" size="100%">Celestino, C.</style></author><author><style face="normal" font="default" size="100%">Toribio, M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">OBTENCION DE PLANTAS A PARTIR DE EMBRIONES SOMATICOS DE QUERCUS SUBER L</style></title><secondary-title><style face="normal" font="default" size="100%">Congreso Forestal Español, Lourizán - Pontevedra. 1993</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">adventive embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">culture media</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">secondary embryogenesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1993</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1993///</style></date></pub-dates></dates><pages><style face="normal" font="default" size="100%">337 - 341</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">This paper gives a procedure to regenerate plants of cork oak through somatic embryogenesis. The somatic embryos were obtained in leaves from young seedlings and cotyledonary fragments from mature acorns of cork oak. The explants were cultured in three stage process in wich BA and NAA concentration were decreasing. Different methods were used to germinate the embryos. Dessication and culture in low salt concentration medium were chosen to give the best results</style></abstract><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;periodical: Congreso Forestal Español, Lourizán - Pontevedra. 1993</style></notes></record><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%">FERRAN, A.</style></author><author><style face="normal" font="default" size="100%">Vallejo, V. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Litter dynamics in post-fire successional forests of Quercus ilex</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Ecology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">C/N ratio</style></keyword><keyword><style  face="normal" font="default" size="100%">Decay coefficient</style></keyword><keyword><style  face="normal" font="default" size="100%">Holm oak</style></keyword><keyword><style  face="normal" font="default" size="100%">mediterranean forest</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1992</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1992///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/p30r4492qt193p64.pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">99-100</style></volume><pages><style face="normal" font="default" size="100%">239 - 246</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Forest floor regeneration after fire in a holm oak forest was studied in a chronosequence in Catalonia (NE Spain). The sampled area represented situations of high fire disturbance because of the frequency of wildfires and the high impact of erosive processes. Forest floor bulk samples from the L, F and H layers were taken in 5 burned plots, aging from 0 to 35 years. They were analyzed for dry standing weight, and organic carbon and N content. Plant cover reached almost 100°o two years after the fire. During the first 20 years, shrubs and herbs had the highest surface covering, and thereafter, holm oaks became dominant. Holm oak litterfall stabilized by the fourth year after burning. The major shrub species which were present in the chronosequence had two different patterns with respect to nitrogen: 1) a low litter C/N ratio (i.e. nitrogen fixing species); 2) a high litter C/N ratio. The litter decay coefficients were relatively high, allowing for a rapid structuration and formation of the L and F layers after the fire. Indeed, 95 ° o of the maximum steady standing weight accumulates in 8-9 years. The pattern of cover in the different strata influenced the lateral distribution and variable accumulation of the forest floor layers and determined different turnover rates.</style></abstract></record><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%">Bueno, M. A.</style></author><author><style face="normal" font="default" size="100%">Astorga, R.</style></author><author><style face="normal" font="default" size="100%">Manzanera, J. A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Plant regeneration through somatic embryogenesis in Quercus suber</style></title><secondary-title><style face="normal" font="default" size="100%">Physiologia Plantarum</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%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">tissue culture</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1992</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1992///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1399-3054.1992.tb05259.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">85</style></volume><pages><style face="normal" font="default" size="100%">30 - 34</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Cork oak (Quercus suber L.) zygotic embryos, endosperm and ovules were treated with different concentrations of 2,4-D for induction of somatic embryos. Plant material was collected during the embryo development season, from June to September. Immature embryos proved to be the most reactive initial explant. Callus and somatic embryos developed a few weeks after the beginning of the 2,4-D treatment. For embryo development experiments, different growth regulators and cold and desiccation treatments were tested. Cold storage of somatic embryos matured in vitro at 5°C was the best treatment for breaking dormancy.</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;publisher: Blackwell Publishing Ltd</style></notes></record><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%">TORIBIO, M</style></author><author><style face="normal" font="default" size="100%">CELESTINO, C</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cultivo in vitro del alcornoque</style></title><secondary-title><style face="normal" font="default" size="100%">Scientia gerundensis</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%">micropropagation</style></keyword><keyword><style  face="normal" font="default" size="100%">plant regeneration</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">tissue culture</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1989</style></year></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">11-21</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Vegetative plant propagation is mainly used in the operational line of Forest Tree Improvement Programs to capture all the genetic potential, including the non-additive component of the genetic variance. In the case of genus Quercus, it could be also used to avoid the problems derived from installation and yielding of seed orchards. The tissue culture based micropropagation arises as an alternative technique to solve the problems of space and time associated with the classical techniques of asexual propagation. This article reviews the work done with cork-oak in this field. Up to date there are few papers dealing with in vitro culture of Quercus suher L. Embryo culture has been tryed to determine the minimum requeriments of the species and its morphogenic potential. Plantlet regeneration has been obtained following axillary budding on nodal segments from juvenile and rejuvenated tissues, elongation and rooting of microcuttings. Main problems arise on transplanting soil the neoformed plants. Callus culture has been achieved from cotyledons and epicotyl segments from young seedlings. In booth cases also somatic embryogenesis has been reported. This fact opens a new way for micropropagating cork-oak, which is discussed.</style></abstract></record></records></xml>