<?xml version="1.0" encoding="UTF-8"?><xml><records><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%">JIMENEZ, J</style></author><author><style face="normal" font="default" size="100%">ALONSO BLÁZQUEZ, N</style></author><author><style face="normal" font="default" size="100%">HERNÁNDEZ, I</style></author><author><style face="normal" font="default" size="100%">CARNEROS, E</style></author><author><style face="normal" font="default" size="100%">CUENCA, B</style></author><author><style face="normal" font="default" size="100%">OCAÑA, L</style></author><author><style face="normal" font="default" size="100%">RUIZ, M</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><author><style face="normal" font="default" size="100%">J., ALEGRE</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efecto de las características del biorreactor y de su manejo sobre el desarrollo de cultivos embriogénicos de alcornoque</style></title><secondary-title><style face="normal" font="default" size="100%">V Congreso Forestal Español</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biotecnología forestal</style></keyword><keyword><style  face="normal" font="default" size="100%">embriogénesis somática</style></keyword><keyword><style  face="normal" font="default" size="100%">medio líquido</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><pub-location><style face="normal" font="default" size="100%">Avila</style></pub-location><pages><style face="normal" font="default" size="100%">1-11</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">En el marco del proyecto SEFEAL-2, liderado por TRAGSA, se aplican protocolos de embriogénesis somática (ES) para desarrollar variedades de alcornoque de alta calidad y productividad. Al mismo tiempo se mejora la técnica de ES para abaratar los costes y permitir su aplicación a escala comercial. En el alcornoque, como en otras especies, el desarrollo comercial de la embriogénesis como técnica de multiplicación masiva se basa en el uso de biorreactores y medios líquidos agitados. El diseño del biorreactor, su sistema de cierre y el nivel de agitación determinan el grado de mezclado, el estrés hidrodinámico y el intercambio gaseoso, y por ello afectan tanto al crecimiento como al desarrollo de los cultivos embriogénicos. Mediante un ensayo factorial se testaron 3 tipos de envase y tres niveles de agitación. Los efectos sobre el intercambio gaseoso se estimaron a través de la tasa de transferencia de O2 (OTR) y su coeficiente volumétrico de transferencia de masa (KLa), y los efectos sobre el nivel de mezclado mediante el “shear force index” (SFI), un indicador de estrés hidrodinámico. El tipo de envase afectó básicamente al número total de agregados embriogénicos y a la frecuencia de formación de los agregados de mayor tamaño. El nivel de agitación tuvo mayores efectos que el tipo de envase tanto sobre el número como sobre el tamaño de los agregados. Para las condiciones ensayadas, que dieron lugar a valores de KLa comprendidos entre 0,11 h-1 y 1,47 h-1, la disponibilidad de oxígeno no pareció limitante. En cualquier caso, los efectos del tipo de envase y del nivel de agitación sobre los procesos de crecimiento y desarrollo de los materiales embriogénicos de alcornoque fueron complejos resultando muy significativa la interacción tipo de envase por nivel de agitación</style></abstract></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%">HERNÁNDEZ, I</style></author><author><style face="normal" font="default" size="100%">CUENCA, B</style></author><author><style face="normal" font="default" size="100%">CARNEROS, E</style></author><author><style face="normal" font="default" size="100%">ALONSO BLÁZQUEZ, N</style></author><author><style face="normal" font="default" size="100%">RUIZ, M</style></author><author><style face="normal" font="default" size="100%">CELESTINO, C</style></author><author><style face="normal" font="default" size="100%">OCAÑA, L</style></author><author><style face="normal" font="default" size="100%">ALEGRE, J</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%">Regeneración clonal de alcornoques selectos mediante embriogénesis somática</style></title><secondary-title><style face="normal" font="default" size="100%">V Congreso Forestal Español</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biotecnología forestal</style></keyword><keyword><style  face="normal" font="default" size="100%">clonación</style></keyword><keyword><style  face="normal" font="default" size="100%">cultivo in vitro</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword><keyword><style  face="normal" font="default" size="100%">silvicultura multivarietal</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><pub-location><style face="normal" font="default" size="100%">Avila</style></pub-location><pages><style face="normal" font="default" size="100%">1-13</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Para implementar la silvicultura multivarietal se precisa disponer de una metodología de propagación vegetativa eficiente y económicamente viable. La embriogénesis somática se está asentando como la vía de clonación más adecuada para las especies forestales consideradas recalcitrantes. En el IMIDRA hemos logrado poner a punto un protocolo de inducción de embriogénesis somática en hojas de alcornoques adultos, aplicable a cualquier genotipo, que permite clonar árboles selectos. En el marco del proyecto SEFEAL-2, liderado por TRAGSA, se está aplicando este protocolo con el objetivo de clonar 70 árboles seleccionados por su calidad y productividad en procedencias extremeñas, a fin de establecer los oportunos ensayos clonales que permitan evaluar dicho material para su inclusión en el Catálogo Nacional de Materiales de Base, en la categoría controlado. Hasta el momento se ha trabajado con 59 genotipos, en 51 de ellos se han obtenido brotes epicórmicos y por tanto hojas para inducir embriogénesis, lográndose líneas embriogénicas en 44 de estos últimos. Por tanto, al primer intento se ha logrado la inducción en un 86% de los genotipos ensayados. Se indujo embriogénesis en un 17 % de las hojas introducidas en cultivo, variando la frecuencia con el genotipo entre 0 y 56%. Las líneas se amplificaron por embriogénesis recurrente y los embriones, tanto madurados espontáneamente como sometidos a un tratamiento de maduración, fueron estratificados y dispuestos a germinar. Los porcentajes de conversión a plántula oscilaron en función del genotipo entre el 37 y el 75% para los embriones sometidos a un tratamiento de maduración, y entre el 9 y el 87% para los madurados espontáneamente. La supervivencia media de las vitroplantas regeneradas de embriones que maduraron espontáneamente fue del 17%, variando en función del genotipo entre 0 y 33%, mientras que las que procedieron de embriones somáticos sometidos a tratamiento de maduración fue del 26%, oscilando entre el 12 y el 52% según genotipos. Palabras</style></abstract></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%">CELESTINO, C</style></author><author><style face="normal" font="default" size="100%">HERNÁNDEZ, I</style></author><author><style face="normal" font="default" size="100%">Lopez-Vela, D</style></author><author><style face="normal" font="default" size="100%">CARNEROS, E</style></author><author><style face="normal" font="default" size="100%">ALEGRE, J</style></author><author><style face="normal" font="default" size="100%">TORIBIO, M</style></author><author><style face="normal" font="default" size="100%">Fernández-Guijarro, B</style></author><author><style face="normal" font="default" size="100%">Cardo, L</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Santamaria, JM and Desjardins, Y</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">First data from a field trial of Quercus suber plants regenerated from mature selected trees and from their half-sib progenies by somatic embryogenesis</style></title><secondary-title><style face="normal" font="default" size="100%">Proceedings of the Second International Symposium on Acclimatization and Establishment of Micropropagated Plants</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%">field establishment</style></keyword><keyword><style  face="normal" font="default" size="100%">rejuvenation</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">woody plant micro-propagation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><publisher><style face="normal" font="default" size="100%">INTERNATIONAL SOCIETY HORTICULTURAL SCIENCE</style></publisher><pub-location><style face="normal" font="default" size="100%">PO BOX 500, 3001 LEUVEN 1, BELGIUM</style></pub-location><pages><style face="normal" font="default" size="100%">215-218</style></pages><isbn><style face="normal" font="default" size="100%">978-90-6605-550-6</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Somatic embryogenesis is considered as the most suitable current regeneration technique for the conservation and genetic improvement of tree species. The ability to induce somatic embryogenesis in leaves from mature trees gives the possibility to compare the performance of the parent trees and their progenies at the same age and place of test. Somatic seedlings were regenerated from five selected cork oak trees and from young plants of their half-sib progenies. They were planted in the field conjointly with zygotic seedlings of these families, to test the comparisons somatic vs. zygotic origin and somatic from mature trees vs. somatic from juvenile seedlings. The effect of genotype and kind of progeny will be studied in a complete factorial design; therefore the field trial comprised 15 treatments arranged in five completely randomised blocks. Each experimental unit included three plants that were distributed following a row and column pattern. Fist survival and height data after six and twelve months of establishment are provided. All plants from seeds survived while almost the half of somatic seedlings died after the winter and they were replaced. Almost 70% of these plants survived after the following summer. There were no differences between somatic seedlings of mature or juvenile origin. Zygotic seedlings doubled the height of the somatic ones after one year in the field, and within these plants those of mature origin grew slightly more than those of juvenile source. Differences due to genotype and family effects were noticeable. No apparent morphological alterations were detected among the three kinds of tested progenies.</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%">Álvarez, R</style></author><author><style face="normal" font="default" size="100%">Alonso, P</style></author><author><style face="normal" font="default" size="100%">Cortizo, M</style></author><author><style face="normal" font="default" size="100%">CELESTINO, C</style></author><author><style face="normal" font="default" size="100%">HERNÁNDEZ, I</style></author><author><style face="normal" font="default" size="100%">TORIBIO, M</style></author><author><style face="normal" font="default" size="100%">Ordás, R J</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Genetic transformation of selected mature cork oak (Quercus suber L.) trees.</style></title><secondary-title><style face="normal" font="default" size="100%">Plant cell reports</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Agrobacterium</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">Fagaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Tree genetic transformation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2004</style></year></dates><volume><style face="normal" font="default" size="100%">23</style></volume><pages><style face="normal" font="default" size="100%">218-223</style></pages><isbn><style face="normal" font="default" size="100%">3498510479</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A transformation system for selected mature cork oak (Quercus suber L.) trees using Agrobacterium tumefaciens has been established. Embryos obtained from recurrent proliferating embryogenic masses were inoculated with A. tumefaciens strains EHA105, LBA4404 or AGL1 harbouring the plasmid pBINUbiGUSint [carrying the neomycin phosphotransferase II (nptII) and beta-glucuronidase (uidA) genes]. The highest transformation efficiency (4%) was obtained when freshly isolated explants were inoculated with A. tumefaciens strain AGL1. Evidence of stable transgene integration was obtained by PCR for the nptII and uidA genes, Southern blotting and expression of the uidA gene. The transgenic embryos were germinated and successfully transferred to soil.</style></abstract><accession-num><style face="normal" font="default" size="100%">15185122</style></accession-num></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%">HERNÁNDEZ, I</style></author><author><style face="normal" font="default" size="100%">CELESTINO, C</style></author><author><style face="normal" font="default" size="100%">ALEGRE, J</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%">Vegetative propagation of Quercus suber L. by somatic embryogenesis. II. Plant regeneration from selected cork oak trees.</style></title><secondary-title><style face="normal" font="default" size="100%">Plant cell reports</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Clonal propagation</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">Selected trees</style></keyword><keyword><style  face="normal" font="default" size="100%">Somatic embryogenesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year></dates><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">765-770</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The regeneration of somatic seedlings from selected 100-year-old cork oak trees is reported. The induction of somatic embryogenesis from leaves of epicormic shoots was significantly affected by genotype, harvesting time and their interaction. Leaves from all five selected trees produced somatic embryos when the segments of branches used as sources of epicormic shoots were collected in May. Genotype, but not the level of photosynthetically active radiation, affected the proliferation of the embryogenic lines and the number of detachable embryos that could be obtained from them. Genotype also affected several steps leading to conversion of somatic embryos, from germination to complete acclimatisation of somatic seedlings. Almost 40% of the somatic embryos from all lines germinated, showing coordinated root and shoot growth. Although the mean percentage of recovery for the whole process was low, plants could be regenerated from four of the five trees tested.</style></abstract><accession-num><style face="normal" font="default" size="100%">12789520</style></accession-num></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%">HERNÁNDEZ, I</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%">Vegetative propagation of Quercus suber L. by somatic embryogenesis. I. Factors affecting the induction in leaves from mature cork oak trees.</style></title><secondary-title><style face="normal" font="default" size="100%">Plant cell reports</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Clonal propagation</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork oak</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></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year></dates><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">759-764</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Somatic embryogenesis was induced in expanding leaves from epicormic shoots forced to sprout from segments of branches collected from several hundred-year-old cork oak trees. Following a basic protocol previously defined for leaves taken from seedlings of this species, several factors were studied to improve the response. The induction frequency was significantly higher when the length of exposure to growth regulators was increased from 7 to 30 days. The combined application of NAA and BAP was essential for induction. Although both regulators had a very significant influence, their interaction was not significant, suggesting independent roles. Leaf size had a crucial effect, because beyond a certain threshold, embryogenesis could not be obtained. Embryogenic lines were maintained via repetitive embryogenesis on hormone-free medium for more than 2 years.</style></abstract><accession-num><style face="normal" font="default" size="100%">12789519</style></accession-num></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%">HERNÁNDEZ, I</style></author><author><style face="normal" font="default" size="100%">Gallardo, J F</style></author><author><style face="normal" font="default" size="100%">Regina, I Santa</style></author><author><style face="normal" font="default" size="100%">Quilchano, C</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Decomposition rate of Quercus rotundifolia leaves in an evergreen oak forest of the Duero Basin (Province of Zamora, Spain)</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%">forest ecosystems</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf decomposition</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1992</style></year></dates><volume><style face="normal" font="default" size="100%">99-100</style></volume><pages><style face="normal" font="default" size="100%">259-262</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Experimental litter decomposition of Quercus rotundifolia leaves in an evergreen oak forest of the semiarid area of the Duero Basin has been carried out. The loss of weight of the decomposing oak leaves was 623, j, after 24 months. In general, it is physical factors (mainly precipitation) which limit the decompo- sition of the evergreen oak leaves. Different patterns of bioelement losses were observed, increasing the relative content of N and P, and decreasing the amounts of Mg, K and Na in the decomposing leaves.</style></abstract></record></records></xml>