<?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%">Şen, Ali</style></author><author><style face="normal" font="default" size="100%">Van den Bulcke, Jan</style></author><author><style face="normal" font="default" size="100%">Defoirdt, Nele</style></author><author><style face="normal" font="default" size="100%">Van Acker, Joris</style></author><author><style face="normal" font="default" size="100%">Pereira, Helena</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermal behaviour of cork and cork components</style></title><secondary-title><style face="normal" font="default" size="100%">Thermochimica Acta</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cork</style></keyword><keyword><style  face="normal" font="default" size="100%">DSC</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus cerris</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">suberin</style></keyword><keyword><style  face="normal" font="default" size="100%">TGA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2014///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0040603114000902</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">582</style></volume><pages><style face="normal" font="default" size="100%">94 - 100</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Thermal behaviour of cork and cork chemical components was studied with coupled differential scanning calorimetry-thermogravimetrical analysis (DSC-TGA) in order to gain insight into the role of the chemical components on the thermal degradation of cork. Cork samples of Turkey oak (Quercus cerris) and cork oak (Quercus suber) were chemically treated to selectively remove inorganic material, extractives and suberin, to allow characterization of klason lignin and methanolysis-depolymerized suberin. Since Q. cerris cork granulates contain phloemic impurities, phloem from Q. cerris bark was also subjected to the same treatments as cork. The thermal decomposition of both cork species is similar, starting above 200°C and increasing with increasing temperature until ashing at approximately 485°C. TGA curves of both corks are almost identical but a detailed view on the differential thermogravimetry (DTG) and DSC curves shows that the two materials differ from each other. Two exothermal devolatilization and char combustion reactions occur, peaking at approximately 313°C and 445°C. These peak temperatures shift to lower temperatures in suberin-free and extractive-free corks giving evidence of the heat retarding effect of suberin and extractives and possible catalytic effect of inorganics in desuberinised cork. Phloem thermal degradation is similar to that of cork although exothermal peak temperatures are higher. Phloem-containing Q. cerris cork granulates thus show clear potential for high temperature applications.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Variability of the Chemical Composition of Cork</style></title><secondary-title><style face="normal" font="default" size="100%">BioResources</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">2246-2256</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The chemical composition of cork was determined, following a sampling that covered the whole production area in Portugal (29 provenances from six regions) with samples taken at cork stripping. To analyse between population variations, a more intensive sampling was made in two locations. The overall mean chemical composition of cork was: extractives 16.2% (dichloromethane 5.8%, ethanol 5.9%, water 4.5%), suberin 42.8% (long-chain lipids 41.0%, glycerol 3.8%), and lignin 22.0% (Klason 21.1%, acid soluble 0.9%). The suberin compositional ratio of long chain lipids to glycerol, LCLip:Gly, was 11.3. The proportion of neutral sugars in the polysaccharides was: glucose 46.1%, xylose 25.1%, arabinose 18.0%, mannose 3.0%, galactose 7.3%, and rhamnose 0.5%. The range of values was large and the variation between individual trees seemed to be the major factor of the differences. Geographical location of cork production was statistically significant only in a few cases when considering site and not when considering regions. The population variation in two sites was important and the absolute difference between the site mean values was small. This research covers the natural variability of cork’s chemical composition and discusses the contribution of the structural compounds to the variation of cork properties.</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%">Aguado, Pedro L.</style></author><author><style face="normal" font="default" size="100%">Curt, M. Dolores</style></author><author><style face="normal" font="default" size="100%">Pereira, Helena</style></author><author><style face="normal" font="default" size="100%">Fernández, Jesús</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Allocation of 14C assimilated in late spring to tissue and biochemical stem components of cork oak (Quercus suber L.) over the seasons</style></title><secondary-title><style face="normal" font="default" size="100%">Tree Physiology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">C-14 labeled compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">carbon assimilation</style></keyword><keyword><style  face="normal" font="default" size="100%">microautoradiography</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">suberin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2012///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://treephys.oxfordjournals.org/content/32/3/313.abstract</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">32</style></volume><pages><style face="normal" font="default" size="100%">313 - 325</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Carbon distribution in the stem of 2-year-old cork oak plants was studied by 14CO2 pulse labeling in late spring in order to trace the allocation of photoassimilates to tissue and biochemical stem components of cork oak. The fate of 14C photoassimilated carbon was followed during two periods: the first 72 h (short-term study) and the first 52 weeks (long-term study) after the 14CO2 photosynthetic assimilation. The results showed that 14C allocation to stem tissues was dependent on the time passed since photoassimilation and on the season of the year. In the first 3 h all 14C was found in the polar extractives. After 3 h, it started to be allocated to other stem fractions. In 1 day, 14C was allocated mostly to vascular cambium and, to a lesser extent, to primary phloem; no presence of 14C was recorded for the periderm. However, translocation of 14C to phellem was observed from 1 week after 14CO2 pulse labeling. The phellogen was not completely active in its entire circumference at labeling, unlike the vascular cambium; this was the tissue that accumulated most photoassimilated 14C at the earliest sampling. The fraction of leaf-assimilated 14C that was used by the stem peaked at 57% 1 week after 14CO2 plant exposure. The time lag between C photoassimilation and suberin accumulation was ∼8 h, but the most active period for suberin accumulation was between 3 and 7 days. Suberin, which represented only 1.77% of the stem weight, acted as a highly effective sink for the carbon photoassimilated in late spring since suberin specific radioactivity was much higher than for any other stem component as early as only 1 week after 14C plant labeling. This trend was maintained throughout the whole experiment. The examination of microautoradiographs taken over 1 year provided a new method for quantifying xylem growth. Using this approach it was found that there was more secondary xylem growth in late spring than in other times of the year, because the calculated average cell division time was much shorter.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">10.1093/treephys/tps01210.1093/treephys/tps012</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Cellular structure and chemical composition of cork from the Chinese cork oak (Quercus variabilis)</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Wood Science</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Quercus variabilis Blume, the Chinese cork oak, is an oak species with a thick cork outer bark. The cork is exploited at a limited scale in China and considered of lower quality than the commercial cork from Quercus suber. We studied an industrial cork granulate feedstock of Q. variabilis in relation to cellular structure and chemical composition and compared it to Q. suber cork under a material’s perspective. The cork of Q.variabilis has 1.1 % ash, 9.6 % extractives, 34.8 % suberin and 19.1 % lignin. The monosaccharide composition with shows a predominance of hemicelluloses: glucose 42.8 % of total neutral sugars, xylose 27.5 %, arabinose 15.4 %, galactose 9.0 %, mannose 4.0 %, rhamnose 1.2 %. The FT-IR spectrum shows the indicative peaks of suberin. The composition is overall similar to that of Q. suber cork. Q. variabilis cork has the typical cellular characteristics of bark cork tissues with a regular and radially aligned structure of cells without intercellular voids. Solid volume fraction was estimated at approximately 16 %. Compared with Q. suber, the Q. variabilis cork cells are smaller, the cell wall undulation and the overall row alignment less homogeneous, the cell surface is irregular and the solid volume proportion higher. The characteristics of Q. variabilis cork support its use as a cellular material for sealing, insulation and energy absorption, but the overall quality is lower than that of Q. suber cork. The negative impact of the higher density and structural lower uniformity at tissue and cell level should be evaluated for processing and product performance.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Lignin monomeric composition of corks from the barks of Betula pendula, Quercus suber and Quercus cerris determined by Py–GC–MS/FID</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Analytical and Applied Pyrolysis</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier B.V.</style></publisher><pages><style face="normal" font="default" size="100%">1-7</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Samples of cork tissues separated from the barks of Betula pendula, Quercus suber and Quercus cerris were characterized by Py–GC–MS/FID in respect to composition of lignin. The pyrolysis temperature influenced the yield of pyrolysis products, and in the conditions usually applied to wood pyrolysis (550 ◦C) suberin is only partially degraded into products. The lignin composition of the three corks showed predominantly a guaiacyl-based lignin: guaiacyl (G) units represented 85.7%, 96.4% and 93.7% of lignin respectively in B. pendula, Q. suber and Q. cerris corks, while syringyl (S) units amounted respectively to 11.9%, 2.5% and 2.7% and p-hydroxyphenyl (H) units to 2.4%, 1.1% and 3.6%. Pyrolysis of the woods of these same species confirmed the GS character of their lignins in contrast to the corks G-lignin type. The influence of ferulic acid in the results and its integration in a heterogeneous cork lignin structure was discussed.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">The cellular structure of cork from Quercus cerris var. cerris bark in a materials’ perspective</style></title><secondary-title><style face="normal" font="default" size="100%">Industrial Crops and Products</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year></dates><volume><style face="normal" font="default" size="100%">34</style></volume><pages><style face="normal" font="default" size="100%">929-936</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Cork in the outer bark of trees is among the valuable raw materials of biological origin due to properties that result mainly from its cellular structure. Large scale commercial utilization of cork has been only achieved with cork from Quercus suber. Another oak species, Quercus cerris, also contains substantial, albeit not continuous, regions of cork that are clearly visible to the naked eye but are so far considered as a waste material. Bark samples of Q. cerris var. cerris trees were collected from the Andırın province, Turkey. Cork portions were separated and their cellular structure was investigated with optical and electron scanning microscopy observations. The results were compared with Q. suber cork. Q. cerris cork has the typical features of cork tissues with a regular and radially aligned structure of suberized cells without intercellular voids, showing a ring structure and a distinction of earlycork and latecork cells. Solid volume fraction was estimated at 25% (22% in earlycork, 36% in latecork). In Q. cerris cork cells are smaller, cell wall thickness and solid volume fraction are higher, and the tissue is less homogeneous with a higher content of ligniﬁed inclusions than in Q. suber cork. These factors will negatively inﬂuence quality in regard to density and mechanical properties associated to elasticity. However, this does not impair its use for production of granulates and agglomerates, e.g. for insulation and energy absorption. Separation of the cork fraction from the bark is a step required before further processing and use.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Vessel size and number are contributors to define wood density in cork oak</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Forest Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year></dates><volume><style face="normal" font="default" size="100%">130</style></volume><pages><style face="normal" font="default" size="100%">1023-1029</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.) has a dense wood that allows high-quality uses. In the present work, we study the inﬂuence of vessel characteristics, measured through image analysis and optical microscopy, on wood density, measured using X-ray microdensitometry, on 40-year-old trees. Vessel area increases with cambial age (5403–33064 lm 2 ), while wood density decreases (1.229–0.836 g/cm 3 ). The number of vessels is relatively constant at 6 vessels/mm 2 , while vessel proportion in cross-section increases from 3.3% near the pith to 20.5% near the bark. In growth rings closest to the pith, with high wood density and low vessel area, the relationship between the two variables is linear (R 2 = -32.1%, P\0.01) but with increasing tree age and vessel size, the wood density remains rather constant, suggesting that decreases in density might compromise mechanical support of the tree at a stage when the increase in crosssectional area alone might not provide mechanical stability. Other anatomical characteristics not considered in this study, like large xylem rays that increase with cambial age, may be responsible for the constant density</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%">Teixeira, Rita Teresa</style></author><author><style face="normal" font="default" size="100%">Pereira, Helena</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Suberized Cell Walls of Cork from Cork Oak Differ from Other Species</style></title><secondary-title><style face="normal" font="default" size="100%">Microscopy and Microanalysis</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">cell wall</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork</style></keyword><keyword><style  face="normal" font="default" size="100%">lamellae</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">suberin</style></keyword><keyword><style  face="normal" font="default" size="100%">ultrastructure</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2010///</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">569 - 575</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Plants have suberized cells that act as protective interfaces with the environment or between different plant tissues. A lamellar structure of alternating dark and light bands has been found upon transmission electron microscopy (TEM) observation of cork cells and considered a typical feature of the suberized secondary wall. We observed cork cells from periderms of Quercus suber, Quercus cerris, Solanum tuberosum, and Calotropis procera by TEM after uranyl acetate and lead citrate staining. A lamellated structure was observed in S. tuberosum and C. procera but not in Q. suber and Q. cerris where the suberized cell wall showed a predominantly hyaline aspect with only a dark dotted staining. Removal of suberin from Q. suber cells left a thinner secondary wall that lost the translucent aspect. We hypothesize that the species' specific chemical composition of suberin will result in different three-dimensional macromolecular development and in a different spatial location of lignin and other aromatics. A lamellated ultrastructure is therefore not a general feature of suberized cells.</style></abstract><issue><style face="normal" font="default" size="100%">5</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%">Teixeira, Rita Teresa</style></author><author><style face="normal" font="default" size="100%">Pereira, Helena</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ultrastructural Observations Reveal the Presence of Channels between Cork Cells</style></title><secondary-title><style face="normal" font="default" size="100%">MICROSCOPY AND MICROANALYSIS</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calotropis procera</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork</style></keyword><keyword><style  face="normal" font="default" size="100%">phellogen</style></keyword><keyword><style  face="normal" font="default" size="100%">plasmodesmata</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">suberin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2009///</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">539 - 544</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The ultrastructure of phellem cells of Quercus Silber L. (cork oak) and Calotropis procera (Ait) R. Br. were analyzed using electron transmission microscopy to determine the presence or absence of plasmodesmata (PD). Different types of Q. Silber cork samples were studied: one year shoots; virgin cork (first periderm), reproduction cork (traumatic periderm), and wet cork. The channel structures of PD were found in all the samples crossing adjacent cell walls through the suberin layer of the secondary wait. Calotropis phellem also showed PD crossing the cell walls of adjacent cells but in fewer numbers compared to Q. suber. In one year stems of cork oak, it was possible to follow the physiologically active PD with ribosomic accumulation next to the aperture of the channel seen in the phellogen cells to the completely obstructed channels in the dead cells that characterize the phellem tissue.</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;pub-location: 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA&lt;br/&gt;publisher: CAMBRIDGE UNIV PRESS</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Ultrastructural Observations Reveal the Presence of Channels between Cork Cells</style></title><secondary-title><style face="normal" font="default" size="100%">MICROSCOPY AND MICROANALYSIS</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><publisher><style face="normal" font="default" size="100%">CAMBRIDGE UNIV PRESS</style></publisher><pub-location><style face="normal" font="default" size="100%">32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA</style></pub-location><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">539-544</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The ultrastructure of phellem cells of Quercus Silber L. (cork oak) and Calotropis procera (Ait) R. Br. were analyzed using electron transmission microscopy to determine the presence or absence of plasmodesmata (PD). Different types of Q. Silber cork samples were studied: one year shoots; virgin cork (first periderm), reproduction cork (traumatic periderm), and wet cork. The channel structures of PD were found in all the samples crossing adjacent cell walls through the suberin layer of the secondary wait. Calotropis phellem also showed PD crossing the cell walls of adjacent cells but in fewer numbers compared to Q. suber. In one year stems of cork oak, it was possible to follow the physiologically active PD with ribosomic accumulation next to the aperture of the channel seen in the phellogen cells to the completely obstructed channels in the dead cells that characterize the phellem tissue.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Radial variation of vessel size and distribution in cork oak wood (Quercus suber L.)</style></title><secondary-title><style face="normal" font="default" size="100%">Wood Science and Technology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><volume><style face="normal" font="default" size="100%">41</style></volume><pages><style face="normal" font="default" size="100%">339-350</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Quercus suber L. is an important species producing cork whose wood characteristics have not been investigated a lot. Cork oak wood vessels are a striking feature and the most abundant wood tissue largely inﬂuencing density and permeability. Vessel size and distribution were studied in approximately 40 year-old and never debarked cork oaks by continuously measuring along the radial direction in the transverse section of wood discs taken at 1.3 m of height using image analysis techniques. The vessel size increases with age from 7660 ± 2286 to 21136 ± 6119 lm 2 , the conductive area from 5.4 ± 2.2 to 11.6 ± 3.9%, and the vessel density remains approximately constant between 5.2 ± 1.5 and 7.3 ± 3.5 vessels/mm 2 . In comparison with ring-porous and some evergreen oaks, cork oaks show a similar conductive area but smaller vessels. Vessel architecture is known to play an important role on oaks tolerance to hydric stress, and these cork oak trees were growing under very harsh edaphoclimatic conditions, not tolerated by other oaks. The well-developed and deep root system allowing access to constant water supply may contribute to the cork oak’s relatively high conductive area.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>3</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">SEASONAL PATTERN OF PHYSIOLOGICAL STATE IN A CORK OAK (QUERCUS SUBER L.) STAND IN HUELVA (SPAIN)</style></title><secondary-title><style face="normal" font="default" size="100%">Suberwood2005: New challenges for integration of cork oak forests and products, Scientific and Technical Conference, Huelva, Spain, 20, 21 and 22 October 2005.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><publisher><style face="normal" font="default" size="100%">Universidad de Huelva</style></publisher><pub-location><style face="normal" font="default" size="100%">Huelva</style></pub-location><pages><style face="normal" font="default" size="100%">456</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The seasonal pattern of the physiological state of Quercus suber is determined by different ecological factors, and it affects to the growth of the species. The main objective of this study is to know the seasonal pattern of water potential, photosynthesis and fluorescence in four Quercus suber L. trees and to relate these values with ecological factors during two years. In this time there were three critical periods, the first one the end of the dry period where the water potential descends to values less than -3MPa and the photosynthesis to 0.781 µmol CO2m-2 s-1Quercus suber, physiology, water potential, photosynthesis, fluorescence. . The second critical period is located in period of change of the leaf, between the months of March and May. The third critical period occurred due to the freezes and drought of the year 2005, that produced strong damages in the PSII.</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%">GONZÁLEZ-PÉREZ, ARANTZAZU</style></author><author><style face="normal" font="default" size="100%">VÁZQUEZ-PIQUÉ, JAVIER</style></author><author><style face="normal" font="default" size="100%">TAPIAS, RAÚL</style></author><author><style face="normal" font="default" size="100%">FERNÁNDEZ, MANUEL</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">VÁZQUEZ-PIQUÉ, JAVIER</style></author><author><style face="normal" font="default" size="100%">Pereira, Helena</style></author><author><style face="normal" font="default" size="100%">GONZÁLEZ-PÉREZ, ARANTZAZU</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">SEASONAL PATTERN OF PHYSIOLOGICAL STATE IN A CORK OAK (QUERCUS SUBER L.) STAND IN HUELVA (SPAIN)</style></title><secondary-title><style face="normal" font="default" size="100%">Suberwood2005: New challenges for integration of cork oak forests and products, Scientific and Technical Conference, Huelva, Spain, 20, 21 and 22 October 2005.</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">fluorescenc</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">water potential</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2005///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Universidad de Huelva</style></publisher><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The seasonal pattern of the physiological state of Quercus suber is determined by different ecological factors, and it affects to the growth of the species. The main objective of this study is to know the seasonal pattern of water potential, photosynthesis and fluorescence in four Quercus suber L. trees and to relate these values with ecological factors during two years. In this time there were three critical periods, the first one the end of the dry period where the water potential descends to values less than -3MPa and the photosynthesis to 0.781 µmol CO2m-2 s-1Quercus suber, physiology, water potential, photosynthesis, fluorescence. . The second critical period is located in period of change of the leaf, between the months of March and May. The third critical period occurred due to the freezes and drought of the year 2005, that produced strong damages in the PSII.</style></abstract><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;periodical: Suberwood2005: New challenges for integration of cork oak forests and products, Scientific and Technical Conference, Huelva, Spain, 20, 21 and 22 October 2005.&lt;br/&gt;pub-location: Huelva</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">The periderm development in Quercus suber</style></title><secondary-title><style face="normal" font="default" size="100%">IAWA Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year></dates><volume><style face="normal" font="default" size="100%">25</style></volume><pages><style face="normal" font="default" size="100%">325-335</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In the cork oak (Quercus suber L.), the phellogen differentiates during the first year of growth in the cell layer immediately under the epidermis and divides to form 3–6 suberized phellem cells. Division of the phellogen only occurs after suberization of the previous divided cell. During the first four years of growth, the phellem cells have tannin-filled lumens and it is only in the 5th to 7th years that they acquire the characteristics of ʻadultʼ cork cells with empty lumens and thin suberized walls. The len- ticels are formed by the lenticular phellogen, which differentiates under the stomata and has a high meristematic activity. In this region, the cells are unsuberized, with a loose arrangement and intercellular voids, consti- tuting the filling or complementary tissue. After three years, the lenticels appear as small protuberances that soon become conspicuous. Inclusions of sclerenchymatous nodules and isolated sclereids occur occasionally mostly in the vicinity of, or in, the lenticels.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Methanolysis of bark suberins: analysis of glycerol and acid monomers</style></title><secondary-title><style face="normal" font="default" size="100%">Phytochemical Analysis</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2000</style></year></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">45-51</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The depolymerization and subsequent analysis of cork suberins from the outer barks of Pseudotsuga menziesii and Quercus suber was performed using a simpliﬁed methanolysis procedure. The amount of sodium methoxide catalyst was maintained at 20–30 mM and the methanolysis mixture was submitted to trimethylsilyl derivatisation and used directly for gas chromatographic analysis, allowing simultaneous quantiﬁcation of glycerol and long-chain monomers. Response factors for glycerol, ferulic acid and one saturated homologue representing each of the suberinic families (i.e. the 1-alkanols, 1-alkanoic acids, vhydroxyacids and a,v-diacids) were determined. Effective depolymerization of suberin was checked using the infrared specta of the residues after methanolysis. Glycerol is a major constituent of the suberins from P. menziesii (26% of total) and from Q. suber (14%). In both suberins, a,v-diacids are dominant, i.e. 54% of the long-chain monomers in P. menziesii (mostly saturated C16-C22 homologues and the C18 unsaturated diacid), and 53% in Q. suber (mostly the C18 unsaturated diacid and mid-chain oxygenated (epoxide and vic-diol) derivatives). In P. menziesii epoxyacids are absent. The importance of glycerol and a,v-diacids as suberin monomers supports a polymeric structure based on their successive esteriﬁcation.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">Cork Suberin: A Glyceryl Based Polyester</style></title><secondary-title><style face="normal" font="default" size="100%">Holzforschung - International Journal of the Biology, Chemistry, Physics and Technology of Wood</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1997</style></year></dates><volume><style face="normal" font="default" size="100%">51</style></volume><pages><style face="normal" font="default" size="100%">225-234</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Total depolymerization of cork from the cork oak (Quercus suber L.) by using a sodium methoxide catalysed methanolysis solubilized 53.2 % of the material, including 5.2 % of glycerol, 48,0 % of suberinic fatty acids and alcohols and minor amounts of ferulic acid. A very mild depolymerization using calcium oxide treated methanol, which solubilized only 2.0% of the cork material was studied by GC-MS. In the solubilized material, the total amount of aliphatic acids was 43.8 % (including alkanoic acids 4.0%. ω-hydroxyacids 13.2% and α,ω-diacids 26.6%), of 1-alkanols 2.1 % and of monoacylglycenols 32.1%. It was possible to identify 1-monoacylglycerols and 2-monoacylglycerols of alkanoic acids (1,2%), ω-hydroxyacids (3.7 %) and α,ω-diacids (22.8 %). It is proposed that suberin is a glyceryl based polymer and that its insoluble character is given, at least in part, by the cross-linking of dicarboxylic fatty acids with glycerol. The term suberin should be used for this aliphatic polyester component of the cell wall.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors></contributors><titles><title><style face="normal" font="default" size="100%">THE CELLULAR STRUCTURE OF CORK FROM QUERCUS SUBER L</style></title><secondary-title><style face="normal" font="default" size="100%">IAWA Bulletin</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1987</style></year></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">213-218</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The main characteristics of the cellular struc- ture of cork from Quercus suber L. are review- ed and comph;mented with new observations of virgin and reproduction cork by scanning electron microscopy. Particular emphasis is given to cell geometry and topology and to the corrugations that are observed in the cell walls. The effect of the growth season in these fea- tures is described. Large variations in cell size, wall thickness ajld corrugations are reported. Key words: Quercus SIlber, cork, cell gcometry, topology, cell wall corrugations.</style></abstract></record></records></xml>