<?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%">GRATANI, L.</style></author><author><style face="normal" font="default" size="100%">Bonito, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Leaf traits variation during leaf expansion in Quercus ilex L.</style></title><secondary-title><style face="normal" font="default" size="100%">Photosynthetica</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf expansion</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf morphology</style></keyword><keyword><style  face="normal" font="default" size="100%">net photosynthetic rate</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</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><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/J6N552465N18M216.pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">323 - 330</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The morphological, anatomical and physiological variations of leaf traits were analysed during Quercus ilex L. leaf expansion. The leaf water content (LWC), leaf area relative growth rate (RGRl ) and leaf dry mass relative growth rate (RGRm) were the highest (76±2 %, 0.413 cm 2 cm –2 d –1 , 0.709 mg mg –1 d –1 , respectively) at the beginning of the leaf expansion process (7 days after bud break). Leaf expansion lasted 84±2 days when air temperature ranged from 13.3±0.8 to 27.6±0.9 °C. The net photosynthetic rate (PN), stomatal conductance (gs ), and chlorophyll content per fresh mass (Chl) increased during leaf expansion, having the highest values [12.62±1.64 µmol (CO2) m –2 s –1 , 0.090 mol (H2O) m –2 s –1 , and 1.03±0.08 mg g –1 ,respectively] 56 days after bud break. Chl was directly correlated with leaf dry mass (DM) and PN. The thickness of palisade parenchyma contributed to the total leaf thickness (263.1±1.5 μm) by 47 %, spongy layer thickness 38 %, adaxial epidermis and cuticle thickness 9 %, and abaxial epidermis and cuticle thickness 6 %. Variation in leaf size during leaf expansion might be attributed to a combination of cells density and length, and it is confirmed by the significant (p&lt;0.001) correlations among these traits. Q. ilex leaves reached 90 % of their definitive structure before the most severe drought period (beginning of June – end of August). The high leaf mass area (LMA, 15.1±0.6 mg cm –2 ) at full leaf expansion was indicative of compact leaves (2028±100 cells mm –2 ). Air temperature increasing might shorten the favourable period for leaf expansion, thus changing the final amount of biomass per unit leaf area of Q. ilex.</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%">Serrano, L.</style></author><author><style face="normal" font="default" size="100%">Penuelas, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Contribution of physiological and morphological adjustments to drought resistance in two Mediterranean tree species</style></title><secondary-title><style face="normal" font="default" size="100%">Biologia Plantarum</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Drought stress</style></keyword><keyword><style  face="normal" font="default" size="100%">net photosynthetic rate</style></keyword><keyword><style  face="normal" font="default" size="100%">phillyrea latifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">plant and tissue-water relations</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</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><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/pm645l6757200722.pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">49</style></volume><pages><style face="normal" font="default" size="100%">551 - 559</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Plant water potential (ψ), its components, and gas exchange data of two Mediterranean co-occurring woody species (Quercus ilex L. and Phillyrea latifolia L.) were measured in response to seasonal changes in water availability over two consecutive years. The relative contribution of physiological and morphological adjustments to drought resistance was assessed through Principal Component Analyses. There were large adjustments in stomatal conductance (~36 % of accounted variance). Net photosynthetic rate and water use efficiency were closely tuned to water availability and accounted for ~17 % of variance. The slope of the water potential vs. relative water content (dψ/dRWC0) below zero pressure potential increased as a result of seasonal and ontogenic increases in apoplastic water fraction and accounted for ~20 % variance. This tolerance mechanism was accompanied by an increased range of positive pressure potential, suggesting a functional role of sclerophylly in these Mediterranean evergreens. Similarly, changes in the slope of dψ/dRWC in the range of positive pressure potential (~13 % of accounted variance) were associated to variations in cell wall elasticity and resulted in lower RWC at zero pressure potential. When considering the species studied separately, the results indicated the primary role of stomatal regulation in the drought resistance of Q. ilex, while increased apoplastic water fraction had a major contribution in the drought resistance of P. latifolia.</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue></record></records></xml>