<?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%">Büker, P.</style></author><author><style face="normal" font="default" size="100%">Morrissey, T.</style></author><author><style face="normal" font="default" size="100%">Briolat, A.</style></author><author><style face="normal" font="default" size="100%">Falk, R.</style></author><author><style face="normal" font="default" size="100%">Simpson, D.</style></author><author><style face="normal" font="default" size="100%">Tuovinen, J.-P.</style></author><author><style face="normal" font="default" size="100%">Alonso, R.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Baumgarten, M.</style></author><author><style face="normal" font="default" size="100%">Grulke, N.</style></author><author><style face="normal" font="default" size="100%">Karlsson, P. E.</style></author><author><style face="normal" font="default" size="100%">King, J.</style></author><author><style face="normal" font="default" size="100%">Lagergren, F.</style></author><author><style face="normal" font="default" size="100%">Matyssek, R.</style></author><author><style face="normal" font="default" size="100%">Nunn, A.</style></author><author><style face="normal" font="default" size="100%">Ogaya, R.</style></author><author><style face="normal" font="default" size="100%">Penuelas, J.</style></author><author><style face="normal" font="default" size="100%">Rhea, L.</style></author><author><style face="normal" font="default" size="100%">Schaub, M.</style></author><author><style face="normal" font="default" size="100%">Uddling, J.</style></author><author><style face="normal" font="default" size="100%">Werner, W.</style></author><author><style face="normal" font="default" size="100%">Emberson, L. D.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">DO3SE modelling of soil moisture to determine ozone flux to forest trees</style></title><secondary-title><style face="normal" font="default" size="100%">Atmospheric Chemistry and Physics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">DO3SE</style></keyword><keyword><style  face="normal" font="default" size="100%">Drought (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">Modeling</style></keyword><keyword><style  face="normal" font="default" size="100%">soil water</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal ozone ﬂux</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://www.atmos-chem-phys.net/12/5537/2012/</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">5537 - 5562</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The DO3SE (Deposition of O3 for Stomatal Exchange) model is an established tool for estimating ozone (O3) deposition, stomatal ﬂux and impacts to a variety of vegetation types across Europe. It has been embedded within the EMEP (European Monitoring and Evaluation Programme) photochemical model to provide a policy tool capable of relating the ﬂux-based risk of vegetation damage to O3 precursor emission scenarios for use in policy formulation. A key limitation of regional ﬂux-based risk assessments has been the assumption that soil water deﬁcits are not limiting O3 ﬂux due to the unavailability of evaluated methods for modelling soil water deﬁcits and their inﬂuence on stomatal conductance (gsto), and subsequent O3 ﬂux. This paper describes the development and evaluation of a method to estimate soil moisture status and its inﬂuence on gsto for a variety of forest tree species. This DO3SE soil moisture module uses the Penman-Monteith energy balance method to drive water cycling through the soil-plantatmosphere system and empirical data describing gsto relationships with pre-dawn leaf water status to estimate the biological control of transpiration. We trial four different methods to estimate this biological control of the transpiration stream, which vary from simple methods that relate soil water content or potential directly to gsto, to more complex methods that incorporate hydraulic resistance and plant capacitance that control water ﬂow through the plant system. These methods are evaluated against ﬁeld data describing a variety of soil water variables, gsto and transpiration data for Norway spruce (Picea abies), Scots pine (Pinus sylvestris), birch (Betula pendula), aspen (Populus tremuloides), beech (Fagus sylvatica) and holm oak (Quercus ilex) collected from ten sites across Europe and North America. Modelled estimates of these variables show consistency with observed data when applying the simple empirical methods, with the timing and magnitude of soil drying events being captured well across all sites and reductions in transpiration with the onset of drought being predicted with reasonable accuracy. The more complex methods, which incorporate hydraulic resistance and plant capacitance, perform less well, with predicted drying cycles consistently underestimating the rate and magnitude of water loss from the soil. A sensitivity analysis showed that model performance was strongly dependent upon the local parameterisation of key model drivers such as the maximum gsto, soil texture, root depth and leaf area index. The results suggest that the simple modelling methods that relate gsto directly to soil water content and potential provide adequate estimates of soil moisture and inﬂuence on gsto such that they are suitable to be used to assess the potential risk posed by O3 to forest trees across Europe.</style></abstract><issue><style face="normal" font="default" size="100%">12</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%">de Andrés, Juan Manuel</style></author><author><style face="normal" font="default" size="100%">Borge, Rafael</style></author><author><style face="normal" font="default" size="100%">de la Paz, David</style></author><author><style face="normal" font="default" size="100%">Lumbreras, Julio</style></author><author><style face="normal" font="default" size="100%">Rodríguez, Encarnación</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Implementation of a module for risk of ozone impacts assessment to vegetation in the Integrated Assessment Modelling system for the Iberian Peninsula. Evaluation for wheat and Holm oak.</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental pollution (Barking, Essex : 1987)</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Air Pollutants</style></keyword><keyword><style  face="normal" font="default" size="100%">Air Pollutants: analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Air Pollutants: toxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Chemical</style></keyword><keyword><style  face="normal" font="default" size="100%">CMAQ WRF</style></keyword><keyword><style  face="normal" font="default" size="100%">Critical level</style></keyword><keyword><style  face="normal" font="default" size="100%">Environmental Monitoring</style></keyword><keyword><style  face="normal" font="default" size="100%">Environmental Monitoring: methods</style></keyword><keyword><style  face="normal" font="default" size="100%">iberian peninsula</style></keyword><keyword><style  face="normal" font="default" size="100%">Models</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone risk assessment</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone: analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone: toxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Portugal</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus: drug effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus: growth &amp; development</style></keyword><keyword><style  face="normal" font="default" size="100%">Risk Assessment</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">Triticum</style></keyword><keyword><style  face="normal" font="default" size="100%">Triticum: drug effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Triticum: growth &amp; development</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://www.ncbi.nlm.nih.gov/pubmed/22398018</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">165</style></volume><pages><style face="normal" font="default" size="100%">25 - 37</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A module to estimate risks of ozone damage to vegetation has been implemented in the Integrated Assessment Modelling system for the Iberian Peninsula. It was applied to compute three different indexes for wheat and Holm oak; daylight AOT40 (cumulative ozone concentration over 40 ppb), cumulative ozone exposure index according to the Directive 2008/50/EC (AOT40-D) and POD(Y) (Phytotoxic Ozone Dose over a given threshold of Y nmol m(-2) s(-1)). The use of these indexes led to remarkable differences in spatial patterns of relative ozone risks on vegetation. Ozone critical levels were exceeded in most of the modelling domain and soil moisture content was found to have a significant impact on the results. According to the outputs of the model, daylight AOT40 constitutes a more conservative index than the AOT40-D. Additionally, flux-based estimations indicate high risk areas in Portugal for both wheat and Holm oak that are not identified by AOT-based methods.</style></abstract><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;publisher: Elsevier Ltd&lt;br/&gt;accession-num: 22398018</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%">Calatayud, Vicent</style></author><author><style face="normal" font="default" size="100%">Cerveró, Júlia</style></author><author><style face="normal" font="default" size="100%">Calvo, Esperanza</style></author><author><style face="normal" font="default" size="100%">García-Breijo, Francisco-José</style></author><author><style face="normal" font="default" size="100%">Reig-Armiñana, José</style></author><author><style face="normal" font="default" size="100%">Sanz, María José</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Responses of evergreen and deciduous Quercus species to enhanced ozone levels.</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental pollution (Barking, Essex : 1987)</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Critical levels</style></keyword><keyword><style  face="normal" font="default" size="100%">Functional leaf traits</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</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.ncbi.nlm.nih.gov/pubmed/20974507</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">159</style></volume><pages><style face="normal" font="default" size="100%">55 - 63</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Plants of one evergreen oak (Quercus ilex) and three deciduous oaks (Q. faginea, with small leaves; Q. pyrenaica and Q. robur, with large leaves) were exposed both to filtered air and to enhanced ozone levels in Open-Top Chambers. Q. faginea and Q. pyrenaica were studied for the first time. Based on visible injury, gas exchange, chlorophyll content and biomass responses, Q. pyrenaica was the most sensitive species, and Q. ilex was the most tolerant, followed by Q. faginea. Functional leaf traits of the species were related to differences in sensitivity, while accumulated ozone flux via stomata (POD1.6) partly contributed to the observed differences. For risk assessment of Mediterranean vegetation, the diversity of responses detected in this study should be taken into account, applying appropriate critical levels.</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: Elsevier Ltd&lt;br/&gt;accession-num: 20974507</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-Barradas, Mari Cruz</style></author><author><style face="normal" font="default" size="100%">Zunzunegui, María</style></author><author><style face="normal" font="default" size="100%">Ain-Lhout, Fatima</style></author><author><style face="normal" font="default" size="100%">Jáuregui, Juan</style></author><author><style face="normal" font="default" size="100%">Boutaleb, Said</style></author><author><style face="normal" font="default" size="100%">Álvarez-Cansino, Leonor</style></author><author><style face="normal" font="default" size="100%">Esquivias, Mari Paz</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Seasonal physiological responses of Argania spinosa tree from Mediterranean to semi-arid climate</style></title><secondary-title><style face="normal" font="default" size="100%">Plant and Soil</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Browsing</style></keyword><keyword><style  face="normal" font="default" size="100%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf traits</style></keyword><keyword><style  face="normal" font="default" size="100%">photochemical efficiency</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">water relations</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><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/10.1007/s11104-010-0518-8</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">337</style></volume><pages><style face="normal" font="default" size="100%">217 - 231</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Argania spinosa (the argan tree) is a slowgrowing tree endemic of Morocco, growing on semiarid areas where no other tree species can live. With the aim of predicting temporal changes in A. spinosa woodlands under a probable increase in aridity, we set off to investigate these questions: how do A. spinosa physiological attributes respond to variations in climatic conditions and seasonality, and which is the set of attributes that most affects tree response to environmental conditions? In three study sites, Beni Snassen (North), High-Atlas (Mountain) and Admine Forest in Agadir (Coastal), gas exchange measurements, photochemical efficiency, leaf water potential and different leaf attributes were monitored in February, July and November of 2006. The Mountain site presents the most continental climate. Trees in this site were the most stressed in summer, having the lowest midday leaf water potential values, photochemical efficiency and assimilation rates. We found a Ψmd threshold around -4 MPa, below which stomatal conductance responds linearly to Ψmd . Plants from the North area never reached this threshold during the study period. Although leaf pigments presented a clear seasonal pattern, leaves from Coastal trees exhibit the highest content for each season. The three study sites were separated by two discriminate functions obtained by canonical discriminant analysis. In summer, the Mountain population is separated from the other sites mainly by assimilation rate and Fv /Fm, while in winter transpiration rates and chlorophyll content are the main discriminant variables. Our study shows that A. spinosa trees adjust their physiological status and leaf attributes to environmental conditions allowing plants to thrive under a dry climate. Under a scenario of global change, the distribution of the argan tree likely shifts to milder areas.</style></abstract><issue><style face="normal" font="default" size="100%">1-2</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%">Cuesta, Bárbara</style></author><author><style face="normal" font="default" size="100%">Villar-Salvador, Pedro</style></author><author><style face="normal" font="default" size="100%">Puértolas, Jaime</style></author><author><style face="normal" font="default" size="100%">Jacobs, Douglass F.</style></author><author><style face="normal" font="default" size="100%">Rey Benayas, José M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Why do large, nitrogen rich seedlings better resist stressful transplanting conditions? A physiological analysis in two functionally contrasting Mediterranean forest species</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">competition</style></keyword><keyword><style  face="normal" font="default" size="100%">Nitrogen remobilization</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Pinus halepensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">Root growth</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">Survival</style></keyword><keyword><style  face="normal" font="default" size="100%">water potential</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><urls><web-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0378112710001957</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">260</style></volume><pages><style face="normal" font="default" size="100%">71 - 78</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">We analysed the physiological bases that explain why large and high nitrogen (N) concentration seedlings frequently have improved survival and growth relative to small seedlings in Mediterranean woodland plantations. Large seedlings of Aleppo pine (Pinus halepensisMill.) and holm oak (Quercus ilex L.) with high N concentration (L+), and small seedlings with either high (S+) or low (S−) N concentration, were planted on two sites of different weed competition intensity that created contrasting stress conditions. Seedling survival, growth, gas exchange, N remobilization (NR) and uptake (NU), and water potential were assessed through the ﬁrst growing season. Weeds reduced survival and growth, but seedling response to weed competition varied among phenotypes and between species. At the end of the ﬁrst growing season, L+ Aleppo pine seedlings had higher survival than both small seedling types in presence of weeds but no differences were observed in absence of weeds. Mortality differences among phenotypes occurred in spring but not in summer. L+ Aleppo pines grew more than small Aleppo pines independently of weed competition. No holm oak seedling type survived in presence of weeds and no mortality differences among phenotypes where observed in absence of weeds, although L+ holm oak seedlings grew more than small seedlings. Mortality and growth differences in Aleppo pine were linked to marked physiological differences among phenotypes while physiological differences were small among holm oak phenotypes. L+ Aleppo pines had greater root growth, gas exchange, NR, and NU than small seedlings, irrespective of their N concentration. Seedling size in Aleppo pine had a greater role in the performance of transplanted seedlings than N concentration. The functional differences among oak phenotypes were small whereas they were large in pine seedlings, which led to smaller differences in transplanting performance in holm oak than in pine. This suggests that the nursery seedling quality improvement for planting in dry sites could depend on the species-speciﬁc phenotypic plasticity and functional strategy. Improved transplanting performance in large Aleppo pine seedlings relative to small seedlings was linked to greater gas exchange, root growth and N cycling.</style></abstract><issue><style face="normal" font="default" size="100%">1</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%">Chirino, E.</style></author><author><style face="normal" font="default" size="100%">Vilagrosa, A.</style></author><author><style face="normal" font="default" size="100%">Hernández, E. I.</style></author><author><style face="normal" font="default" size="100%">Matos, 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%">Effects of a deep container on morpho-functional characteristics and root colonization in Quercus suber L. seedlings for reforestation in Mediterranean climate</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Forest tray</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydraulic conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">root system</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0378112708004507</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">256</style></volume><pages><style face="normal" font="default" size="100%">779 - 785</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In the last decades, reforestation and afforestation programs are being carried out mainly with containerized seedlings. Container design determines the morphological and physiological characteristics of seedlings. However, container characteristics are often the same for plant species with very different growth strategies. The most commonly used nursery containers are relatively shallow and limit tap root growth; consequently, species relying on the early development of a long tap root to escape drought, such as those of the Quercus genus, might need to be cultivated in deep containers. The aim of this paper was to compare the morphological and physiological characteristics of Quercus suber L. seedlings cultivated in shallow containers (CCS-18, depth 18 cm) with seedlings cultivated in deep containers (CCL-30, depth 30 cm). Both container types used were made of high-density polyethylene, cylindrical in shape, open-bottomed, with a diameter of 5 cm, two kinds of vertical ribs on the inside wall showing a cultivation density of 318 seedlings/m2 . At the end of nursery culture, the seedlings cultivated in the CCL-30 deep container presented a longer tap root, higher shoot and root biomass and higher Dickson Quality Index (DQI). Moreover, the CCL-30 seedlings showed a higher root growth capacity (RGC), they reached deep substrate layers faster and they presented higher root hydraulic conductance. These morpho-functional advantages improved the CCL-30 seedling water status, which was expressed by higher stomatal conductance during an imposed drought period</style></abstract><issue><style face="normal" font="default" size="100%">4</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%">Fares, S.</style></author><author><style face="normal" font="default" size="100%">Loreto, F.</style></author><author><style face="normal" font="default" size="100%">Kleist, E.</style></author><author><style face="normal" font="default" size="100%">Wildt, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stomatal uptake and stomatal deposition of ozone in isoprene and monoterpene emitting plants</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">isoprene</style></keyword><keyword><style  face="normal" font="default" size="100%">Monoterpenes</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone uptake</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">reaction chambers</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1055/s-2007-965257</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">44 - 54</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Volatile isoprenoids were reported to protect plants against ozone. To understand whether this could be the result of a direct scavenging of ozone by these molecules, the stomatal and non-stomatal uptake of ozone was estimated in plants emitting isoprene or monoterpenes. Ozone uptake by holm oak (Quercus ilex, a monoterpene emitter) and black poplar (Populus nigra, an isoprene emitter) was studied in whole plant enclosures (continuously stirred tank reactors, CSTR). The ozone uptake by plants was estimated measuring ozone concentration at the inlet and outlet of the reactors, after correcting for the uptake of the enclosure materials. Destruction of ozone at the cuticle or at the plant stems was found to be negligible compared to the ozone uptake through the stomata. For both plant species, a relationship between stomatal conductance and ozone uptake was found. For the poplar, the measured ozone losses were explained by the uptake of ozone through the stomata only, and ozone destruction by gas phase reactions with isoprene was negligible. For the oak, gas phase reactions of ozone with the monoterpenes emitted by the plants contributed significantly to ozone destruction. This was confirmed by two different experiments showing a) that in cases of high stomatal conductance but under low CO2 concentration, a reduction of monoterpene emission was still associated with reduced O3 uptake; and b) that ozone losses due to the gas phase reactions only can be measured when using the exhaust from a plant chamber to determine the gas phase reactivity in an empty reaction chamber. Monoterpenes can therefore relevantly scavenge ozone at leaf level contributing to protection against ozone.</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%">Vitale, Marcello</style></author><author><style face="normal" font="default" size="100%">Salvatori, Elisabetta</style></author><author><style face="normal" font="default" size="100%">Loreto, Francesco</style></author><author><style face="normal" font="default" size="100%">Fares, Silvano</style></author><author><style face="normal" font="default" size="100%">Manes, Fausto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Physiological responses of Quercus ilex Leaves to Water Stress and Acute Ozone Exposure Under Controlled Conditions</style></title><secondary-title><style face="normal" font="default" size="100%">Water, Air, and Soil Pollution</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Gas exchange</style></keyword><keyword><style  face="normal" font="default" size="100%">Holm oak (Quercus ilex)</style></keyword><keyword><style  face="normal" font="default" size="100%">lipoxygenase products</style></keyword><keyword><style  face="normal" font="default" size="100%">monoterpene emission</style></keyword><keyword><style  face="normal" font="default" size="100%">o3 flux</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2007///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/10.1007/s11270-007-9560-4</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">189</style></volume><pages><style face="normal" font="default" size="100%">113 - 125</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The combined effect of water stress and ozone (O3) on stomatal O3 flux, damage to photosynthesis, and detoxification by biogenic volatile organic compounds (BVOC) in Quercus ilex leaves was studied. A 4-weeks O3 exposure (250 ppb, 4 h per day) caused a reduction of photosynthesis and stomatal conductance, which was fully recovered 1 week after the end of the treatment, in well-watered and water-stressed plants. Measurements of stomatal O3 flux revealed a low stomatal flux of the pollutant, which became minimal after stomatal closure caused by water stress. An induction of volatile monoterpenes, important compounds in the O3 scavenging system in Q. ilex, and a burst of lipoxygenase compounds (LOX), which are released as gaseous by-products of membrane peroxidation, was observed after 2–3 weeks of O3 fumigation. However, these compounds were also released in control leaves that were exposed to ozone only briefly, to determine stomatal O3 flux. The low stomatal flux that occurred in water stress conditions helped avoiding permanent damage to Q. ilex leaves, although during the O3 treatment photosynthesis was severely limited by stomatal closure. In well-watered plants, O3 fumigation caused a noticeable increase of nocturnal stomatal conductance. If confirmed on adult plants under field conditions, this effect can imply larger flux of O3 at night and possible detrimental effects of O3 on leaf functions in plants exposed to high nocturnal O3 levels.</style></abstract><issue><style face="normal" font="default" size="100%">1-4</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%">Alonso, R.</style></author><author><style face="normal" font="default" size="100%">Bermejo, V.</style></author><author><style face="normal" font="default" size="100%">Sanz, J.</style></author><author><style face="normal" font="default" size="100%">Valls, B.</style></author><author><style face="normal" font="default" size="100%">Elvira, S.</style></author><author><style face="normal" font="default" size="100%">Gimeno, B. S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stomatal conductance of semi-natural Mediterranean grasslands: implications for the development of ozone critical levels.</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental pollution (Barking, Essex : 1987)</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Critical levels</style></keyword><keyword><style  face="normal" font="default" size="100%">Grasslands</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone</style></keyword><keyword><style  face="normal" font="default" size="100%">Semi-natural vegetation</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2007///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/16895740</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">146</style></volume><pages><style face="normal" font="default" size="100%">692 - 698</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Intra-genus and intra-specific variation and the influence of nitrogen enrichment on net assimilation and stomatal conductance of some annual Trifolium species of Mediterranean dehesa grasslands were assessed under experimental conditions. Also gas exchange rates were compared between some Leguminosae and Poaceae species growing in the field in a dehesa ecosystem in central Spain. The results showed that the previously reported different O3 sensitivity of some Trifolium species growing in pots does not seem to be related to different maximum g(s) values. In addition, no clear differences on gas exchange rates could be attributed to Leguminosae and Poaceae families growing in the field, with intra-genus variation being more important than differences found between families. Further studies are needed to increase the database for developing a flux-based approach for setting O3 critical levels for semi-natural Mediterranean species.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;accession-num: 16895740</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%">Filella, Iolanda</style></author><author><style face="normal" font="default" size="100%">Penuelas, Josep</style></author><author><style face="normal" font="default" size="100%">Llusia, Joan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Dynamics of the enhanced emissions of monoterpenes and methyl salicylate, and decreased uptake of formaldehyde, by Quercus ilex leaves after application of jasmonic acid</style></title><secondary-title><style face="normal" font="default" size="100%">New Phytologist</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Carbon dioxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Carbon Dioxide: metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Cyclopentanes</style></keyword><keyword><style  face="normal" font="default" size="100%">Cyclopentanes: pharmacology</style></keyword><keyword><style  face="normal" font="default" size="100%">Dehydration</style></keyword><keyword><style  face="normal" font="default" size="100%">Formaldehyde</style></keyword><keyword><style  face="normal" font="default" size="100%">Formaldehyde: metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">jasmonic acid (JA)</style></keyword><keyword><style  face="normal" font="default" size="100%">light</style></keyword><keyword><style  face="normal" font="default" size="100%">methyl salicylate</style></keyword><keyword><style  face="normal" font="default" size="100%">Monoterpenes</style></keyword><keyword><style  face="normal" font="default" size="100%">Monoterpenes: metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">net photosynthetic rates</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxylipins</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant Leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant Leaves: drug effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant Leaves: metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex (holm oak)</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus: drug effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus: metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Salicylates</style></keyword><keyword><style  face="normal" font="default" size="100%">Salicylates: metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</style></keyword><keyword><style  face="normal" font="default" size="100%">VOC (volatile organic compound)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2006///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/16390425http://dx.doi.org/10.1111/j.1469-8137.2005.01570.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">169</style></volume><pages><style face="normal" font="default" size="100%">135 - 144</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">* • Jasmonic acid (JA) is a signalling compound with a key role in both stress and development in plants, and is reported to elicit the emission of volatile organic compounds (VOCs). Here we studied the dynamics of such emissions and the linkage with photosynthetic rates and stomatal conductance. * • We sprayed JA on leaves of the Mediterranean tree species Quercus ilex and measured the photosynthetic rates, stomatal conductances, and emissions and uptake of VOCs using proton transfer reaction mass spectrometry and gas chromatography after a dark–light transition. * • Jasmonic acid treatment delayed the induction of photosynthesis and stomatal conductance by approx. 20 min, and decreased them 24 h after spraying. Indications were found of both stomatal and nonstomatal limitations of photosynthesis. Monoterpene emissions were enhanced (20–30%) after JA spraying. Jasmonic acid also increased methyl salicylate (MeSa) emissions (more than twofold) 1 h after treatment, although after 24 h this effect had disappeared. Formaldehyde foliar uptake decreased significantly 24 h after JA treatment. * • Both biotic and abiotic stresses can thus affect plant VOC emissions through their strong impact on JA levels. Jasmonic acid-mediated increases in monoterpene and MeSa emissions might have a protective role when confronting biotic and abiotic stresses.</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&lt;br/&gt;accession-num: 16390425</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%">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><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%">Alessio, G. A.</style></author><author><style face="normal" font="default" size="100%">Lillis, M. De</style></author><author><style face="normal" font="default" size="100%">Fanelli, M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Direct and indirect impacts of fire on isoprenoid emissions from Mediterranean vegetation</style></title><secondary-title><style face="normal" font="default" size="100%">Functional Ecology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">isoprene</style></keyword><keyword><style  face="normal" font="default" size="100%">Mediterranean plant species</style></keyword><keyword><style  face="normal" font="default" size="100%">Monoterpenes</style></keyword><keyword><style  face="normal" font="default" size="100%">Ozone</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">ﬁre ecology</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2004///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://onlinelibrary.wiley.com/doi/10.1111/j.0269-8463.2004.00833.x/full</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">18</style></volume><pages><style face="normal" font="default" size="100%">357 - 364</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">1. Fire is often associated with episodes of air pollution, possibly involving the release of biogenic isoprenoids (isoprene and monoterpenes). The direct and indirect impacts of ﬁre on isoprenoid emission by plants of the Mediterranean vegetation were studied. Leaves of Arbutus unedo, Phillyrea latifolia, Cistus incanus, Cistus mospeliensis, Pistacia lentiscus, Quercus ilex, Quercus suber, Quercus pubescens, Myrtus communis and Pinus halepensis were exposed to direct ﬁre or to the ﬁre-consequent wave of elevated temperature. 2. Half the tested plant species did not emit isoprenoids and the treatments did not induce isoprenoid emission. In contrast, isoprene was emitted by intact leaves of Q. pubescens and M. communis, while monoterpenes were emitted by intact leaves of Q. ilex, Q. suber and P. halepensis. 3. The two treatments rapidly reduced isoprene emission by isoprene-emitting species and monoterpene emission by Quercus spp. This inhibition was associated with photosynthetic inhibition, and recovery was seen in Quercus spp. within days of treatment. Recovery was also associated with the recovery of photosynthesis, suggesting that emitted isoprenoids continue to be formed predominantly from photosynthetic intermediates after a ﬁre episode. 4. In Q. pubescens leaves, however, recovery from the elevated-temperature treatment caused a sustained increase of isoprene emission which was not mirrored by a similar increase in photosynthesis. Whether this represents the induction of alternative metabolic pathways or an increase of the ﬂux of photosynthetic carbon in the isoprene pathway is not known. Isoprene-emitting species in areas surrounding ﬁre may emit a substantially larger hydrocarbon ﬂux for several days after ﬁre. 5. The elevated-temperature treatment induced the emission of α-pinene from Myrtus leaves, and the ﬁre treatment stimulated the emission of several monoterpenes from Pinus needles. The emission began to decrease within minutes in Myrtus, while it increased within the ﬁrst 100 min in Pinus, where it was detectable the day after the event although the ﬂux was smaller than in prestressed needles. 6. Exposure to ﬁre and to the associated elevated temperature may induce bursts of monoterpenes from plants that regularly do not emit these compounds and temporarily increase the load of monoterpenes in the atmosphere by pine species. These emissions may contribute to photochemical reactions involved in smog and ozone formation</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%">Mediavilla, Sonia</style></author><author><style face="normal" font="default" size="100%">Escudero, Alfonso</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stomatal responses to drought of mature trees and seedlings of two co-occurring Mediterranean oaks</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">growth stages</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf water potential</style></keyword><keyword><style  face="normal" font="default" size="100%">mediterranean quercus species</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">vapour pressure deficit</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2004///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0378112703003827</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">187</style></volume><pages><style face="normal" font="default" size="100%">281 - 294</style></pages><isbn><style face="normal" font="default" size="100%">3423294515</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">We studied stomatal responses to decreasing predawn water potential (Cpd ) and increasing leaf-to-air water vapour pressure deﬁcit (VPD) of seedlings and mature trees of two co-occurring Mediterranean oaks with contrasting leaf habits: the evergreen Quercus rotundifolia and the deciduous Quercus faginea. Our objective was to deﬁne and to compare the stomatal strategies of both speciesfordroughtresistanceandtoidentifythepossibledifferencesbetweengrowthstagesinselecteddroughtadaptationattributes. Among the mature trees, Q. rotundifolia exhibited a water-use behaviour that was more conservative than that of Q. faginea: lower maximum stomatal conductances and greater sensitivity to VPD than the deciduous species. As a result, the leaf water potential of the evergreen species never decreased along the day and along the growth season as much as in the deciduous species; this may help to guarantee longer leaf longevity by avoiding irreversible damage during the summer drought. The seedlings of the two species showed a less conservative water-use strategy in comparison with adult trees: a relatively high stomatal conductance and lower stomatal sensitivity to soil and atmospheric drought. As a consequence, leaf water potential decreased more in the seedlings along the day than in the adults. Q. rotundifolia was the species for which the most pronounced differences between growth stages were obtained. Thus, interspeciﬁc differences in response to drought disappeared in the ﬁrst stages of the life of the trees, and the seedlings of the two species showed a common strategy, probably as a response to the competition from the herbaceous layer. A low stomatal sensitivity in beneﬁt of an increase in growth would probably be a more successful strategy under the competitive conditions that seedlings experience during their establishment.</style></abstract><issue><style face="normal" font="default" size="100%">2-3</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%">Penuelas, J.</style></author><author><style face="normal" font="default" size="100%">Filella, I.</style></author><author><style face="normal" font="default" size="100%">Llusia, J.</style></author><author><style face="normal" font="default" size="100%">Siscart, D.</style></author><author><style face="normal" font="default" size="100%">Piñol, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative field study of spring and summer leaf gas exchange and photobiology of the mediterranean trees Quercus ilex and Phillyrea latifolia</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Experimental Botany</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">intrinsic water use efficiency</style></keyword><keyword><style  face="normal" font="default" size="100%">net photosynthetic rates</style></keyword><keyword><style  face="normal" font="default" size="100%">phillyrea latifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">photochemical efficiency</style></keyword><keyword><style  face="normal" font="default" size="100%">photochemical reflectance index</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthetic radiation-use-efficiency</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">reflectance</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">summer</style></keyword><keyword><style  face="normal" font="default" size="100%">water index</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1998///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://jxb.oxfordjournals.org/content/49/319/229.abstract</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">49</style></volume><pages><style face="normal" font="default" size="100%">229 - 238</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Summer-induced changes in gas exchange, fluorescence and reflectance were measured on leaves of two co-occurring Mediterranean small trees, Quercus ilex and Phillyrea latifolia, in May, June and July 1996 in Central Catalonia (NE Spain). The humid 1996 summer only produced mild water stress conditions. However, photosynthesis (A) and stomatal conductance (gs) decreased in June and July in both species. In June P. latifolia had higher net photosynthetic rates and lower stomatal conductances than Q. ilex, thus exhibiting higher instantaneous plant water use efficiencies. In agreement with these results, the photo-chemical reflectance index (PRI, calculated as (R570-R531)/(R531+R570)) of P. latifolia was lower, suggesting a possible lower xanthophyll de-epoxidation state. However, P. latifolia had lower ΔF/F′ and therefore a lower electron transport rate (ETR). The behaviour of PRI confirmed previous studies indicating a strong relationship between PRI, ΔF/F′ , and photosynthetic radiation-use efficiency (PRUE). PRI offers a simple, portable means of assessing PRUE with the potential for remote sensing applications. Finally, the possible ecological consequences of these results on the behaviour of the two species studied under the predicted warmer and drier conditions of global change are discussed.</style></abstract><issue><style face="normal" font="default" size="100%">319</style></issue><notes><style face="normal" font="default" size="100%">10.1093/jxb/49.319.22910.1093/jxb/49.319.229</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%">Filella, I.</style></author><author><style face="normal" font="default" size="100%">Llusia, J.</style></author><author><style face="normal" font="default" size="100%">Piñol, J.</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%">Leaf gas exchange and ﬂuorescence of Phillyrea latifolia, Pistacia lentiscus and Quercus ilex saplings in severe drought and high temperature conditions</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental and Experimental Botany</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">hF/F’m</style></keyword><keyword><style  face="normal" font="default" size="100%">phillyrea latifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthetic rate</style></keyword><keyword><style  face="normal" font="default" size="100%">Pistacia lentiscus</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></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1998///</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">39</style></volume><pages><style face="normal" font="default" size="100%">213 - 220</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Saplings of Phillyrea latifolia, Pistacia lentiscus and Quercus ilex were witheld watering for 7 days, followed by reirrigation. Incident photosynthetic photon ﬂux density (PPFD), leaf temperature, net photosynthetic rates, stomatal conductance, and photochemical efﬁciency of the photosystem II (DF:F’m) were measured three times during the day. The watered plants had higher photosynthetic rates, stomatal conductances, DF:F’m and ETR than non-watered plants. However, watered plants were mildly water stressed as shown by low ratio of variable to maximal ﬂuorescence (Fv:Fm) and high non-photochemical ﬂuorescence quenching (qN). Their DF:F%m was low in the morning and increased in the evening, following the variations in PPFD. Watered plants of Q. ilex had lower photosynthetic activity, stomatal conductance and photosynthetic radiation use efﬁciency than Ph. latifolia and P. lentiscus, and, conversely, reached the highest DF:F%m and ETR. This seems to indicate a different relationship between photosynthetic activity and electron transport rate in Q. ilex compared to the other two species. Ph. latifolia and P. lentiscus appeared to be better adapted to severe drought than Q. ilex.</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%">Roupsard, O.</style></author><author><style face="normal" font="default" size="100%">Gross, P.</style></author><author><style face="normal" font="default" size="100%">Dreyer, E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Limitation of photosynthetic activity by CO2 availability in the chloroplasts of oak leaves from different species and during drought</style></title><secondary-title><style face="normal" font="default" size="100%">Ann. For. Sci.</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">chlorophyll fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">chloroplasts</style></keyword><keyword><style  face="normal" font="default" size="100%">CO2 diffusion</style></keyword><keyword><style  face="normal" font="default" size="100%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">mesophyll conductance</style></keyword><keyword><style  face="normal" font="default" size="100%">oaks</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1996</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1996///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1051/forest:19960207</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">53</style></volume><pages><style face="normal" font="default" size="100%">243 - 254</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">It has recently been suggested that the low photosynthesis rates in tree species as compared to highly productive crops is at least partly due to resistances opposing the CO 2 fluxes in the mesophyll of tree leaves. To validate this assertion, values of CO2 mole fractions in the chloroplasts of leaves from Quercus petraea, Q robur, Q ilex and Populus sp were estimated on the basis of the analysis of the partitioning of light driven electron flow between fractions used for the carboxylation or the oxygenation of RuBP by Rubisco. The procedure used included: i) a measure of total light driven electron flows derived from the chlorophyll a fluorescence ratio ΔF/Fm', which is proportional to the photochemical efficiency of PS II, multiplied by incident irradiance and a calibration coefficient; ii) an estimation of the electron flux devoted to carboxylation obtained from net CO2 assimilation and respiration rate measurement, and using the known electron requirements (four electrons for CO2 or O2 fixation); iii) the derivation of the CO2 mole fraction in the chloroplasts from the specificity factor of Rubisco, and the ratio of carboxylation/oxygenation of RuBP. Results showed that in the absence of drought stress, the mole fraction of CO2 in the chloroplasts (35-45% of the atmospheric one) was much lower than the calculated substomatal one (60-70% of the atmospheric) in all species. Moreover, lowest values were recorded in the species with lowest assimilation rates, suggesting that the differences in the net CO 2 assimilation rate between species are linked to the CO2 availability in the chloroplasts. Finally, the CO2 availability decreased with increasing drought in the soil, stressing the importance of reduced influx of CO2 as an important factor for drought-induced declines of photosynthesis. These results are discussed with respect to the occurrence of significant resistances in the leaf mesophyll, in addition to the stomatal resistances.</style></abstract><issue><style face="normal" font="default" size="100%">2-3</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%">Acherar, M.</style></author><author><style face="normal" font="default" size="100%">Rambal, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative water relations of four Mediterranean oak species</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%">mediterranean species</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus</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><keyword><style  face="normal" font="default" size="100%">water-stress</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/h7524hw511346775.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%">177 - 184</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The water relations and responses of two evergreen (Quercus ilex L. and Q. suber L.) and two decidu- ous (S. afares Pomel. and Q. faginea Will.) Quercus species were studied under experimental conditions. Two-year old seedlings grown in 30 1. pots were subjected to a drying period during which stomatal conductance, pre-dawn potential and minimum foliar potential were measured. The results shows that, for all species, the daily course of stomatal conductance agrees with the patterns proposed by Hinckley et al. (1978 &amp; 1983). Concurrent with the species responses to short-term variation in water availability, it was found that pre-dawn leaf water potential controlled the maximum daily leaf conductance. There was a strong correlation between pre-dawn leaf potential and maximum daily conductance as described by the reciprocal function g ........ = ( -0.47 + 2.61.~bp) 1 for the evergreen oaks and g ......... (-1.94+7.39.~bp) 1 for the deciduous species. These differences between the two groups may partialy explain their geograhic distributions, and suggest general questions concerning the mechanisms which optimize water-use efficiency in Mediterranean oak species.</style></abstract><issue><style face="normal" font="default" size="100%">1930</style></issue></record></records></xml>