<?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%">Vaz, M</style></author><author><style face="normal" font="default" size="100%">Cochard, H</style></author><author><style face="normal" font="default" size="100%">Gazarini, L</style></author><author><style face="normal" font="default" size="100%">Graça, J</style></author><author><style face="normal" font="default" size="100%">Chaves, M M</style></author><author><style face="normal" font="default" size="100%">Pereira, J S</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cork oak (Quercus suber L.) seedlings acclimate to elevated CO2 and water stress: photosynthesis, growth, wood anatomy and hydraulic conductivity</style></title><secondary-title><style face="normal" font="default" size="100%">Trees</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Growth</style></keyword><keyword><style  face="normal" font="default" size="100%">hydraulic conductivity</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaf and wood anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">Soil water stress</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><volume><style face="normal" font="default" size="100%">26</style></volume><pages><style face="normal" font="default" size="100%">1159-1160</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Leaf gas-exchange, leaf and shoot anatomy, wood density and hydraulic conductivity were investigated in seedlings of Quercus suber L. grown for 15 months either at elevated (700 lmol mol -1 ) or normal (350 lmol mol -1 ) ambient atmospheric CO2 concentrations. Plants were grown in greenhouses in a controlled environment: relative humidity 50% (±5), temperature similar to external temperature and natural light conditions. Plants were supplied with nutrients and two water regimes (WW, well watered; WS, water stress). After 6 months exposure to CO2 enrichment an increase in photosynthetic rate, a decrease in stomatal conductance and a decrease in carbon isotope discrimination (D 13 C) were observed, along with enhanced growth and an increase in the number of branches and branch diameter. Over the same period, the shoot weight ratio increased, the root weight ratio decreased and the leaf weight ratio was unaffected. The speciﬁc leaf area increased due to an increase in total leaf thickness, mainly due to the palisade parenchyma and starch. However, after 9 and 15 months of elevated CO2 exposure, the above-mentioned physiological and morphological parameters appeared to be unaffected. Elevated CO2 did not promote changes in vessel lumen diameter, vessel frequency or wood density in stems grown in greenhouse conditions. As a consequence, xylem hydraulic efﬁciency remained unchanged. Likewise, xylem vulnerability to embolism was not modiﬁed by elevated CO2. In summary, elevated CO2 had no positive effect on the ecophysiological parameters or growth of water stressed plants.</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%">Sandoval-Soto, L</style></author><author><style face="normal" font="default" size="100%">Kesselmeier, M</style></author><author><style face="normal" font="default" size="100%">Schmitt, V</style></author><author><style face="normal" font="default" size="100%">Wild, A</style></author><author><style face="normal" font="default" size="100%">Kesselmeier, J</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Observations of the uptake of carbonyl sulfide (COS) by trees under elevated atmospheric carbon dioxide concentrations</style></title><secondary-title><style face="normal" font="default" size="100%">Biogeosciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">beech (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">COS uptake</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Holm oak</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">2935-2945</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">. Global change forces ecosystems to adapt to elevated atmospheric concentrations of carbon dioxide (CO2). We understand that carbonyl sulﬁde (COS), a trace gas which is involved in building up the stratospheric sulfate aerosol layer, is taken up by vegetation with the same triad of the enzymes which are metabolizing CO2, i.e. ribulose-1,5- bisphosphate carboxylase/oxygenase (Rubisco), phosphoenolpyruvate carboxylase (PEP-Co) and carbonic anhydrase (CA). Therefore, we discuss a physiological/biochemical acclimation of these enzymes affecting the sink strength of vegetation for COS. We investigated the acclimation of two European tree species, Fagus sylvatica and Quercus ilex, grown inside chambers under elevated CO2, and determined the exchange characteristics and the content of CA after a 1–2 yr period of acclimation from 350 ppm to 800 ppm CO2. We demonstrate that a compensation point, by deﬁnition, does not exist. Instead, we propose to discuss a point of uptake afﬁnity (PUA). The results indicate that such a PUA, the CA activity and the deposition velocities may change and may cause a decrease of the COS uptake by plant ecosystems, at least as long as the enzyme acclimation to CO2 is not surpassed by an increase of atmospheric COS. As a consequence, the atmospheric COS level may rise causing an increase of the radiative forcing in the troposphere. However, this increase is counterbalanced by the stronger input of this trace gas into the stratosphere causing a stronger energy re- ﬂection by the stratospheric sulfur aerosol into space (Bruhl ¨ et al., 2012). These data are very preliminary but may trigger a discussion on COS uptake acclimation to foster measurements with modern analytical instruments.</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%">Aranjuelo, Iker</style></author><author><style face="normal" font="default" size="100%">Pintó-Marijuan, Marta</style></author><author><style face="normal" font="default" size="100%">Avice, Jean Christophe</style></author><author><style face="normal" font="default" size="100%">Fleck, Isabel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of elevated CO2 on carbon partitioning in young Quercus ilex L. during resprouting</style></title><secondary-title><style face="normal" font="default" size="100%">Rapid Communications in Mass Spectrometry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">carbon allocation</style></keyword><keyword><style  face="normal" font="default" size="100%">Cutting</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Photosynthetic activity (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">Regrowth</style></keyword><keyword><style  face="normal" font="default" size="100%">roots</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://dx.doi.org/10.1002/rcm.4715</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">25</style></volume><pages><style face="normal" font="default" size="100%">1527 - 1535</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Stored carbon (C) represents a very important C pool with residence times of years to decades in tree organic matter. With the objective of understanding C assimilation, partitioning and remobilization in 2-year-old Quercus ilex L., those trees were exposed for 7 months to different [CO2] (elevated: 700 µmol mol−1; and ambient: 350 µmol mol−1 CO2). The 13C-isotopic composition of the ambient CO2 (ca. −12.8‰) was modified (to ca. −19.2‰) under the elevated CO2 conditions in order to analyze C allocation and partitioning before aerial biomass excision, and during the following regrowth (resprouting). Although after 7 months of growth under elevated [CO2], Q. ilex plants increased dry matter production, the absence of significant differences in photosynthetic activity suggests that such an increase was lower than expected. Nitrogen availability was not involved in photosynthetic acclimation. The removal of aboveground organs did not enable the balance between C availability and C requirements to be achieved. The isotopic characterization revealed that before the cutting, C partitioning to the stem (main C sink) prevented leaf C accumulation. During regrowth the roots were the organ with more of the labelled C. Furthermore, developing leaves had more C sink strength than shoots during this period. After the cutting, the amount of C delivered from the root to the development of aboveground organs exceeded the requirements of leaves, with the consequent carbohydrate accumulation. These findings demonstrate that, despite having a new C sink, the responsiveness of those resprouts under elevated [CO2] conditions will be strongly conditioned by the plant's capacity to use the extra C present in leaves through its allocation to other organs (roots) and processes (respiration). Copyright © 2011 John Wiley &amp; Sons, Ltd.</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;publisher: John Wiley &amp; Sons, 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%">FARIA, T.</style></author><author><style face="normal" font="default" size="100%">Vaz, M.</style></author><author><style face="normal" font="default" size="100%">Schwanz, P.</style></author><author><style face="normal" font="default" size="100%">PolIe, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Responses of Photosynthetic and Defence Systems to High Temperature Stress in Quercus suber L Seedlings Grown under Elevated CO2</style></title><secondary-title><style face="normal" font="default" size="100%">Plant biology (Stuttgart, Germany)</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">catalase</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword><keyword><style  face="normal" font="default" size="100%">superoxide dismutase</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</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://onlinelibrary.wiley.com/doi/10.1111/j.1438-8677.1999.tb00265.x/full</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">1</style></volume><pages><style face="normal" font="default" size="100%">365 - 371</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Growth in elevated CO2 led to an increase in biomass production per plant as a result of enhanced carbon uptake and lower rates of respiration, compared to ambient C02-grown plants. No down-regulation of photosynthesis was found after six months of growth under elevated CO2. Photosynthetic rates at 15°C or 35°C were also higher in elevated than in ambient C02-grown plants, when measured at their respective CO2 growth condition. Stomata of elevated C02-grown plants were less responsive to temperature as compared to ambient CO2 plants. The after effect of a heat-shock treatment (4 h at 45°C in a chamber with 80% of relative humidity and 800—1000 tmol rn2 photon flux density) on Amax was less in elevated than in ambient C02-grown plants. At the photochemical level, the negative effect of the heat-shock treatment was slightly more pronounced in ambient than in elevated CO2-grown plants. A greater tolerance to oxidative stress caused by high temperatures in elevated C02-grown plants, in comparison to ambient CO2 plants, is suggested by the increase in superoxide dismutase activity, after 1 h at 45°C, as well as its relatively high activity after 2 and 4 h of the heat shock in the elevated C02-grown plants in contrast with the decrease to residual levels of superoxide dismutase activity in ambient C02-grown plants immediately after 1 h at 45°C. The observed increase in catalase after 1 h at 45°C in both ambient and elevated C02-grown plants, can be ascribed to the higher rates of photorespiration and respiration under this high temperature.</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%">Faria, T</style></author><author><style face="normal" font="default" size="100%">Vaz, M</style></author><author><style face="normal" font="default" size="100%">Schwanz, P</style></author><author><style face="normal" font="default" size="100%">PolIe, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Responses of Photosynthetic and Defence Systems to High Temperature Stress in Quercus suber L Seedlings Grown under Elevated CO2</style></title><secondary-title><style face="normal" font="default" size="100%">Plant biology (Stuttgart, Germany)</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">catalase</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword><keyword><style  face="normal" font="default" size="100%">superoxide dismutase</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">1</style></volume><pages><style face="normal" font="default" size="100%">365-371</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Growth in elevated CO2 led to an increase in biomass production per plant as a result of enhanced carbon uptake and lower rates of respiration, compared to ambient C02-grown plants. No down-regulation of photosynthesis was found after six months of growth under elevated CO2. Photosynthetic rates at 15°C or 35°C were also higher in elevated than in ambient C02-grown plants, when measured at their respective CO2 growth condition. Stomata of elevated C02-grown plants were less responsive to temperature as compared to ambient CO2 plants. The after effect of a heat-shock treatment (4 h at 45°C in a chamber with 80% of relative humidity and 800—1000 tmol rn2 photon flux density) on Amax was less in elevated than in ambient C02-grown plants. At the photochemical level, the negative effect of the heat-shock treatment was slightly more pronounced in ambient than in elevated CO2-grown plants. A greater tolerance to oxidative stress caused by high temperatures in elevated C02-grown plants, in comparison to ambient CO2 plants, is suggested by the increase in superoxide dismutase activity, after 1 h at 45°C, as well as its relatively high activity after 2 and 4 h of the heat shock in the elevated C02-grown plants in contrast with the decrease to residual levels of superoxide dismutase activity in ambient C02-grown plants immediately after 1 h at 45°C. The observed increase in catalase after 1 h at 45°C in both ambient and elevated C02-grown plants, can be ascribed to the higher rates of photorespiration and respiration under this high temperature.</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%">Aranda, Xavier</style></author><author><style face="normal" font="default" size="100%">Agustí, Cristina</style></author><author><style face="normal" font="default" size="100%">Joffre, Richard</style></author><author><style face="normal" font="default" size="100%">Fleck, Isabel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photosynthesis, growth and structural characteristics of holm oak resprouts originated from plants grown under elevated CO2</style></title><secondary-title><style face="normal" font="default" size="100%">Physiologia Plantarum</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Fluorescence (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">Growth</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Resprouts</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://dx.doi.org/10.1111/j.1399-3054.2006.00745.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">128</style></volume><pages><style face="normal" font="default" size="100%">302 - 312</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The physiological characteristics of holm oak (Quercus ilex L.) resprouts originated from plants grown under current CO2 concentration (350 μl l−1) (A-resprouts) were compared with those of resprouts originated from plants grown under elevated CO2 (750 μl l−1) (E-resprouts). At their respective CO2 growth concentration, no differences were observed in photosynthesis and chlorophyll fluorescence parameters between the two kinds of resprout. E-resprouts appeared earlier and showed lower stomatal conductance, higher water-use efficiency and increased growth (higher leaf, stem and root biomass and increased height). Analyses of leaf chemical composition showed the effect of elevated [CO2] on structural polysaccharide (higher cellulose content), but no accumulation of total non-structural carbohydrate on area or dry weight basis was seen. Four months after appearance, downregulation of photosynthesis and electron transport components was observed in E-resprouts: lower photosynthetic capacity, photosystem II quantum efficiency, photochemical quenching of fluorescence and relative electron transport rate. Reduction in ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCo) activity, deduced from the maximum carboxylation velocity of RuBisCo, accounts for the observed acclimation. Increased susceptibility of photosynthetic apparatus to increasing irradiance was detected in E-resprouts.</style></abstract><issue><style face="normal" font="default" size="100%">2</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%">Aranda, Xavier</style></author><author><style face="normal" font="default" size="100%">Agustí, Cristina</style></author><author><style face="normal" font="default" size="100%">Joffre, Richard</style></author><author><style face="normal" font="default" size="100%">Fleck, Isabel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photosynthesis, growth and structural characteristics of holm oak resprouts originated from plants grown under elevated CO2</style></title><secondary-title><style face="normal" font="default" size="100%">Physiologia Plantarum</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Fluorescence (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">Growth</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Resprouts</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2006</style></year></dates><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">128</style></volume><pages><style face="normal" font="default" size="100%">302-312</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The physiological characteristics of holm oak (Quercus ilex L.) resprouts originated from plants grown under current CO2 concentration (350 μl l−1) (A-resprouts) were compared with those of resprouts originated from plants grown under elevated CO2 (750 μl l−1) (E-resprouts). At their respective CO2 growth concentration, no differences were observed in photosynthesis and chlorophyll fluorescence parameters between the two kinds of resprout. E-resprouts appeared earlier and showed lower stomatal conductance, higher water-use efficiency and increased growth (higher leaf, stem and root biomass and increased height). Analyses of leaf chemical composition showed the effect of elevated [CO2] on structural polysaccharide (higher cellulose content), but no accumulation of total non-structural carbohydrate on area or dry weight basis was seen. Four months after appearance, downregulation of photosynthesis and electron transport components was observed in E-resprouts: lower photosynthetic capacity, photosystem II quantum efficiency, photochemical quenching of fluorescence and relative electron transport rate. Reduction in ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCo) activity, deduced from the maximum carboxylation velocity of RuBisCo, accounts for the observed acclimation. Increased susceptibility of photosynthetic apparatus to increasing irradiance was detected in E-resprouts.</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%">KREUZWIESER, JÜRGEN</style></author><author><style face="normal" font="default" size="100%">Cojocariu, Cristian</style></author><author><style face="normal" font="default" size="100%">Jüssen, Vera</style></author><author><style face="normal" font="default" size="100%">RENNENBERG, HEINZ</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Elevated atmospheric CO2 causes seasonal changes in carbonyl emissions from Quercus ilex</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%">Acetaldehyde</style></keyword><keyword><style  face="normal" font="default" size="100%">carbonyl emission</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus pubescens</style></keyword><keyword><style  face="normal" font="default" size="100%">VOC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates><publisher><style face="normal" font="default" size="100%">Blackwell Science Ltd</style></publisher><volume><style face="normal" font="default" size="100%">154</style></volume><pages><style face="normal" font="default" size="100%">327-333</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">* • The effect of elevated atmospheric CO2 on the carbonyl emissions of leaves from two Mediterranean oak species (Quercus ilex and Q. pubescens) was analyzed under field conditions. * • Physiological and meteorological parameters were determined in parallel with measurements of carbonyl emissions. Gas exchange was quantified in dynamic cuvettes combined with an infrared gas analyzer. * • Acetaldehyde and acetone emissions from leaves of Q. ilex were enhanced by elevated CO2 in the autumn (from 14–40 nmol m−2 min−1 and from 2–8 nmol m−2 min−1, respectively), but not in the summer. No significant effects were found for leaves of Q. pubescens. The effects of CO2 on Q. ilex were mainly a result of decreased emissions by control trees under ambient CO2 concentrations in the autumn; emissions from trees exposed to elevated CO2 remained at a high level. * • Elevated atmospheric CO2 causes autumnal changes in carbonyl emissions from Quercus ilex. These effects suggest that the production of acetaldehyde and acetone depend on developmental factors. It is not yet clear whether the altered carbonyl emissions are a unique feature of 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%">Blaschke, L.</style></author><author><style face="normal" font="default" size="100%">Schulte, M.</style></author><author><style face="normal" font="default" size="100%">Raschi, A.</style></author><author><style face="normal" font="default" size="100%">Slee, N.</style></author><author><style face="normal" font="default" size="100%">Rennenberg, H.</style></author><author><style face="normal" font="default" size="100%">Polle, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photosynthesis, Soluble and Structural Carbon Compounds in Two Mediterranean Oak Species (Quercus pubescens and Q. ilex) after Lifetime Growth at Naturally Elevated CO2 Concentrations</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%">Carbohydrate</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Lignin</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Rubisco</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2001///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1055/s-2001-15203</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">3</style></volume><pages><style face="normal" font="default" size="100%">288 - 298</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Abstract: To study physiological responses of mature forest trees to elevated CO2 after lifetime growth under elevated atmospheric CO2 concentrations (pCO2), photosynthesis, Rubisco content, foliar concentrations of soluble sugars and starch, sugar concentrations in transport tissues (phloem and xylem), structural biomass, and lignin in leaves and branches were investigated in 30- to 50-year-old Quercus pubescens and Q. ilex trees grown at two naturally elevated CO2 springs in Italy. Ribulose-1,5-bisphosphate carboxylase/oxygenase content was decreased in Q. pubescens grown under elevated CO2 concentrations, but not in Q. ilex. Photosynthesis was consistently higher in Q. pubescens grown at elevated CO2 as compared with “control” sites, whereas the response in Q. ilex was less pronounced. Stomatal conductance was lower in both species leading to decreased transpiration and increased instantaneous water use efficiency in Q. pubescens. Overall mean sugar + starch concentrations of the leaves were not affected by elevated pCO2, but phloem exudates contained higher concentrations of soluble sugars. This finding suggests increased transport to sinks. Qualitative changes in major carbon-bearing compounds, such as structural biomass and lignins, were only found in bark but not in other tissues. These results support the concept that the maintenance of increased rates of photosynthesis after long-term acclimation to elevated pCO2 provides a means of optimization of water relations under arid climatic conditions but does not cause an increase in aboveground carbon sequestration per unit of tissue in Mediterranean oak 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;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%">Blaschke, L</style></author><author><style face="normal" font="default" size="100%">Schulte, M</style></author><author><style face="normal" font="default" size="100%">Raschi, A</style></author><author><style face="normal" font="default" size="100%">Slee, N</style></author><author><style face="normal" font="default" size="100%">Rennenberg, H</style></author><author><style face="normal" font="default" size="100%">Polle, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photosynthesis, Soluble and Structural Carbon Compounds in Two Mediterranean Oak Species (Quercus pubescens and Q. ilex) after Lifetime Growth at Naturally Elevated CO2 Concentrations</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%">Carbohydrate</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Lignin</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Rubisco</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">3</style></volume><pages><style face="normal" font="default" size="100%">288-298</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Abstract: To study physiological responses of mature forest trees to elevated CO2 after lifetime growth under elevated atmospheric CO2 concentrations (pCO2), photosynthesis, Rubisco content, foliar concentrations of soluble sugars and starch, sugar concentrations in transport tissues (phloem and xylem), structural biomass, and lignin in leaves and branches were investigated in 30- to 50-year-old Quercus pubescens and Q. ilex trees grown at two naturally elevated CO2 springs in Italy. Ribulose-1,5-bisphosphate carboxylase/oxygenase content was decreased in Q. pubescens grown under elevated CO2 concentrations, but not in Q. ilex. Photosynthesis was consistently higher in Q. pubescens grown at elevated CO2 as compared with “control” sites, whereas the response in Q. ilex was less pronounced. Stomatal conductance was lower in both species leading to decreased transpiration and increased instantaneous water use efficiency in Q. pubescens. Overall mean sugar + starch concentrations of the leaves were not affected by elevated pCO2, but phloem exudates contained higher concentrations of soluble sugars. This finding suggests increased transport to sinks. Qualitative changes in major carbon-bearing compounds, such as structural biomass and lignins, were only found in bark but not in other tissues. These results support the concept that the maintenance of increased rates of photosynthesis after long-term acclimation to elevated pCO2 provides a means of optimization of water relations under arid climatic conditions but does not cause an increase in aboveground carbon sequestration per unit of tissue in Mediterranean oak species.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>3</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pereira, J S</style></author><author><style face="normal" font="default" size="100%">Chaves, M M</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mohren, GMJ and Kramer, K and Sabate, S</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Impacts of climate change and elevated CO2 on trees in regions with a Mediterranean type of climate</style></title><secondary-title><style face="normal" font="default" size="100%">IMPACTS OF GLOBAL CHANGE ON TREE PHYSIOLOGY AND FOREST ECOSYSTEMS</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Mediterranean</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees</style></keyword><keyword><style  face="normal" font="default" size="100%">water stress</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><publisher><style face="normal" font="default" size="100%">SPRINGER</style></publisher><pub-location><style face="normal" font="default" size="100%">PO BOX 17, 3300 AA DORDRECHT, NETHERLANDS</style></pub-location><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">213-223</style></pages><isbn><style face="normal" font="default" size="100%">0-7923-4921-0</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Research on the effects of global changes on Mediterranean trees is&lt;br/&gt;still limited. In terms of growth response to elevated CO2,&lt;br/&gt;Mediterranean trees were not different from temperate-zone trees, i.e.,&lt;br/&gt;growth enhancement seems to be short-lived, declining after the first&lt;br/&gt;growing seasons in elevated CO2. In Mediterranean landscapes important&lt;br/&gt;soil fertility gradients can be found. Such differences, mainly in soil&lt;br/&gt;nitrogen, may interact with elevated CO2, as shown by the enhancement of&lt;br/&gt;the response to high CO2 by abundant N in Fraxinus angustifolia (a&lt;br/&gt;deciduous, riparian tree) and Quercus suber (an evergreen oak). Given&lt;br/&gt;the characteristics of the regional climate, special attention in&lt;br/&gt;research was given to the interaction between elevated CO2 and the&lt;br/&gt;summer stress, i.e., heat and high irradiance stresses superimposed on&lt;br/&gt;water deficits. We discuss the possibility that elevated CO2 may&lt;br/&gt;alleviate some of the negative effects of that summer stresses, as was&lt;br/&gt;found in Quercus suber seedlings under controlled conditions or in&lt;br/&gt;Quercus ilex with a life-time exposure to elevated CO2.</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%">Miglietta, F</style></author><author><style face="normal" font="default" size="100%">Raschi, A</style></author><author><style face="normal" font="default" size="100%">Körner, C</style></author><author><style face="normal" font="default" size="100%">Vaccari, F P</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isotope discrimination and photosynthesis of vegetation growing in the Bossoleto CO 2 spring</style></title><secondary-title><style face="normal" font="default" size="100%">Chemosphere</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Grassland vegetation (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">isotopic discrimination</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthetic capacity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><volume><style face="normal" font="default" size="100%">36</style></volume><pages><style face="normal" font="default" size="100%">771-776</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The Bossoleto CO2 spring emits CO2 which has a stable carbon isotopic ratio (~5~3C = - 8%o). We determined ~3C on leaves of several individual species growing in Bossoleto and in a nearby control site at ambient CO,.. ~5t3C was 6% more negative in leaves of species collected from the grassland community of Bossoleto, indicating increased discrimination (A) against the heavy carbon isotope. No such changes were found in ruderal species growing in the same spring, suggesting that photosynthetic capacity was much less affected. A was substantially increased under elevated CO2 in leaves of Quercus pubescens but not in Quercus ilex, which also did not show any increase in non-structural carbohydrates. Gas-exchange measurements made on Plantago lanceolata, supported the view that photosynthetic capacity is decreased in plants grown under elevated CO: and on poor soils</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%">Miglietta, F.</style></author><author><style face="normal" font="default" size="100%">Raschi, A.</style></author><author><style face="normal" font="default" size="100%">Körner, C.</style></author><author><style face="normal" font="default" size="100%">Vaccari, F. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isotope discrimination and photosynthesis of vegetation growing in the Bossoleto CO 2 spring</style></title><secondary-title><style face="normal" font="default" size="100%">Chemosphere</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Grassland vegetation (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">isotopic discrimination</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthetic capacity</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://www.sciencedirect.com/science/article/pii/S0045653597101229</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">36</style></volume><pages><style face="normal" font="default" size="100%">771 - 776</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The Bossoleto CO2 spring emits CO2 which has a stable carbon isotopic ratio (~5~3C = - 8%o). We determined ~3C on leaves of several individual species growing in Bossoleto and in a nearby control site at ambient CO,.. ~5t3C was 6% more negative in leaves of species collected from the grassland community of Bossoleto, indicating increased discrimination (A) against the heavy carbon isotope. No such changes were found in ruderal species growing in the same spring, suggesting that photosynthetic capacity was much less affected. A was substantially increased under elevated CO2 in leaves of Quercus pubescens but not in Quercus ilex, which also did not show any increase in non-structural carbohydrates. Gas-exchange measurements made on Plantago lanceolata, supported the view that photosynthetic capacity is decreased in plants grown under elevated CO: and on poor soils</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%">Paoletti, E.</style></author><author><style face="normal" font="default" size="100%">Nourrisson, G.</style></author><author><style face="normal" font="default" size="100%">Garrec, J. P.</style></author><author><style face="normal" font="default" size="100%">Raschi, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Modifications of the leaf surface structures of Quercus ilex L. in open, naturally CO2-enriched environments</style></title><secondary-title><style face="normal" font="default" size="100%">Plant, Cell &amp; Environment</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf wettability</style></keyword><keyword><style  face="normal" font="default" size="100%">natural CO2 spring</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">stomatal frequency</style></keyword><keyword><style  face="normal" font="default" size="100%">wax amount</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://dx.doi.org/10.1046/j.1365-3040.1998.00358.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">1071 - 1075</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Two Italian CO2 springs allowed us to study the long-term effect of a 350–2600 μmol mol–1 increase in CO2 concentrations on the surface structures of leaves of Quercus ilex L. Carbon dioxide increased the quantity of cuticular waxes, above an apparent threshold of 750 μmol mol–1 CO2. Leaf wettability was not modified by CO2 concentrations. Reduction in stomatal frequency was observable up to 750 μmol mol–1 CO2, the slope being almost the same as that estimated for the increase in CO2 concentration from pre-industrial times to the present. At higher concentrations, CO2 seemed to exert no more impact on stomatal frequency.</style></abstract><issue><style face="normal" font="default" size="100%">10</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%">Paoletti, E</style></author><author><style face="normal" font="default" size="100%">Nourrisson, G</style></author><author><style face="normal" font="default" size="100%">Garrec, J P</style></author><author><style face="normal" font="default" size="100%">Raschi, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Modifications of the leaf surface structures of Quercus ilex L. in open, naturally CO2-enriched environments</style></title><secondary-title><style face="normal" font="default" size="100%">Plant, Cell &amp; Environment</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf wettability</style></keyword><keyword><style  face="normal" font="default" size="100%">natural CO2 spring</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">stomatal frequency</style></keyword><keyword><style  face="normal" font="default" size="100%">wax amount</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">1071-1075</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Two Italian CO2 springs allowed us to study the long-term effect of a 350–2600 μmol mol–1 increase in CO2 concentrations on the surface structures of leaves of Quercus ilex L. Carbon dioxide increased the quantity of cuticular waxes, above an apparent threshold of 750 μmol mol–1 CO2. Leaf wettability was not modified by CO2 concentrations. Reduction in stomatal frequency was observable up to 750 μmol mol–1 CO2, the slope being almost the same as that estimated for the increase in CO2 concentration from pre-industrial times to the present. At higher concentrations, CO2 seemed to exert no more impact on stomatal frequency.</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%">FARIA, T.</style></author><author><style face="normal" font="default" size="100%">Cerasoli, S.</style></author><author><style face="normal" font="default" size="100%">García-Plazaola, J. I.</style></author><author><style face="normal" font="default" size="100%">Guimaraes, M. P.</style></author><author><style face="normal" font="default" size="100%">Abadia, A.</style></author><author><style face="normal" font="default" size="100%">Raschi, A.</style></author><author><style face="normal" font="default" size="100%">Miglietta, F.</style></author><author><style face="normal" font="default" size="100%">Pereira, J. S.</style></author><author><style face="normal" font="default" size="100%">Chaves, M. M.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mohren, GMJ and Kramer</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Photochemical response to summer drought in Quercus ilex trees growing in a naturally CO2 enriched site</style></title><secondary-title><style face="normal" font="default" size="100%">IMPACTS OF GLOBAL CHANGE ON TREE PHYSIOLOGY AND FOREST ECOSYSTEMS</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">water stress</style></keyword><keyword><style  face="normal" font="default" size="100%">xanthophylls</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><publisher><style face="normal" font="default" size="100%">SPRINGER</style></publisher><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">119 - 124</style></pages><isbn><style face="normal" font="default" size="100%">0-7923-4921-0</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The effect of the interaction between water stress and growth at elevated CO2 on the leaf photochemistry were studied in Quercus ilex trees, growing in a naturally CO2 enriched site (the Bossoleto, Italy). Those plants were compared with plants growing nearby in similar soils but at ambient CO2 concentration. Our data indicate that down-regulation of photosynthesis is lower in non-watered trees from the enriched site than in non-watered trees from the ambient-CO2 site This may be associated to the higher carbon availability for the consumption of the excess absorbed light energy or to an increased protection of the photochemical apparatus against oxidative stress in plants grown under elevated CO2.</style></abstract><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;periodical: IMPACTS OF GLOBAL CHANGE ON TREE PHYSIOLOGY AND FOREST ECOSYSTEMS&lt;br/&gt;pub-location: PO BOX 17, 3300 AA DORDRECHT, NETHERLANDS</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>3</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Faria, T</style></author><author><style face="normal" font="default" size="100%">Cerasoli, S</style></author><author><style face="normal" font="default" size="100%">Garcia-Plazaola, J I</style></author><author><style face="normal" font="default" size="100%">Guimaraes, M P</style></author><author><style face="normal" font="default" size="100%">Abadía, A</style></author><author><style face="normal" font="default" size="100%">Raschi, A</style></author><author><style face="normal" font="default" size="100%">Miglietta, F</style></author><author><style face="normal" font="default" size="100%">Pereira, J S</style></author><author><style face="normal" font="default" size="100%">Chaves, M M</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mohren, GMJ and Kramer, K and Sabate, S</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Photochemical response to summer drought in Quercus ilex trees growing in a naturally CO2 enriched site</style></title><secondary-title><style face="normal" font="default" size="100%">IMPACTS OF GLOBAL CHANGE ON TREE PHYSIOLOGY AND FOREST ECOSYSTEMS</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">water stress</style></keyword><keyword><style  face="normal" font="default" size="100%">xanthophylls</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><publisher><style face="normal" font="default" size="100%">SPRINGER</style></publisher><pub-location><style face="normal" font="default" size="100%">PO BOX 17, 3300 AA DORDRECHT, NETHERLANDS</style></pub-location><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">119-124</style></pages><isbn><style face="normal" font="default" size="100%">0-7923-4921-0</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The effect of the interaction between water stress and growth at elevated CO2 on the leaf photochemistry were studied in Quercus ilex trees, growing in a naturally CO2 enriched site (the Bossoleto, Italy). Those plants were compared with plants growing nearby in similar soils but at ambient CO2 concentration. Our data indicate that down-regulation of photosynthesis is lower in non-watered trees from the enriched site than in non-watered trees from the ambient-CO2 site This may be associated to the higher carbon availability for the consumption of the excess absorbed light energy or to an increased protection of the photochemical apparatus against oxidative stress in plants grown under elevated CO2.</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%">Tognetti, Roberto</style></author><author><style face="normal" font="default" size="100%">Johnson, J. D.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Response of foliar metabolism in mature trees of Quercus pubescens and Quercus ilex to long-term elevated CO 2</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%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Gas exchange</style></keyword><keyword><style  face="normal" font="default" size="100%">natural CO2 springs</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary compounds</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://www.sciencedirect.com/science/article/pii/S0098847298000136</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">39</style></volume><pages><style face="normal" font="default" size="100%">233 - 245</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Long-term effects on and adaptations of the carbon physiology of long-lived trees exposed to increasing atmospheric levels of CO2 are unknown. We compared two indigenous Quercus species, Q. ilex and Q. pubescens, growing in a natural CO2 spring located in central Italy and at a nearby control site. In May, 1995 photosynthetic rate at least doubled when measured with supplemental CO2 in both species and sites. Dark respiration was much higher at the CO2 spring site in both species. Foliar sugar and starch concentrations in Q. ilex exhibited signiﬁcant site and diurnal differences (May and September). In July, 1995 there was little difference in the water potential values of the measured trees at the different sites over the diurnal period. Photosynthetic rate was higher for both species in the CO2 spring, particularly in the early morning and late afternoon. Mid-day stomatal closure reduced photosynthesis to similar levels. In the morning leaf conductance and transpiration were generally lower in the CO2 spring trees, contributing to higher instantaneous water use efﬁciency for both species. Isoprene emission rates were higher in Q. pubescens trees growing in the CO2 spring. The maximum difference between control and CO2 spring trees occurred in late afternoon. In contrast, Q. ilex exhibited isoprene emission near background level. Foliage and branch carbon and nitrogen status showed increased concentrations of starch and tannins in Q. ilex and of soluble sugars in Q. pubescens in the elevated CO2 environment, while nitrogen concentration decreased in both species. Wood gravity increased 6 and 3% in Q. ilex and Q. pubescens, respectively, growing in the CO2 spring. Q. ilex exhibited afternoon recovery of water potential compared to Q. pubescens which had better night-time recovery. Q. ilex and Q. pubescens exposed to elevated CO2 for prolonged periods exhibit different mechanisms for dealing with additional reduced carbon and do maintain an altered carbon physiology, even in midst of the region’s characteristic summer drought</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%">Tognetti, Roberto</style></author><author><style face="normal" font="default" size="100%">Johnson, J D</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Response of foliar metabolism in mature trees of Quercus pubescens and Quercus ilex to long-term elevated CO 2</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%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Gas exchange</style></keyword><keyword><style  face="normal" font="default" size="100%">natural CO2 springs</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary compounds</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><volume><style face="normal" font="default" size="100%">39</style></volume><pages><style face="normal" font="default" size="100%">233-245</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Long-term effects on and adaptations of the carbon physiology of long-lived trees exposed to increasing atmospheric levels of CO2 are unknown. We compared two indigenous Quercus species, Q. ilex and Q. pubescens, growing in a natural CO2 spring located in central Italy and at a nearby control site. In May, 1995 photosynthetic rate at least doubled when measured with supplemental CO2 in both species and sites. Dark respiration was much higher at the CO2 spring site in both species. Foliar sugar and starch concentrations in Q. ilex exhibited signiﬁcant site and diurnal differences (May and September). In July, 1995 there was little difference in the water potential values of the measured trees at the different sites over the diurnal period. Photosynthetic rate was higher for both species in the CO2 spring, particularly in the early morning and late afternoon. Mid-day stomatal closure reduced photosynthesis to similar levels. In the morning leaf conductance and transpiration were generally lower in the CO2 spring trees, contributing to higher instantaneous water use efﬁciency for both species. Isoprene emission rates were higher in Q. pubescens trees growing in the CO2 spring. The maximum difference between control and CO2 spring trees occurred in late afternoon. In contrast, Q. ilex exhibited isoprene emission near background level. Foliage and branch carbon and nitrogen status showed increased concentrations of starch and tannins in Q. ilex and of soluble sugars in Q. pubescens in the elevated CO2 environment, while nitrogen concentration decreased in both species. Wood gravity increased 6 and 3% in Q. ilex and Q. pubescens, respectively, growing in the CO2 spring. Q. ilex exhibited afternoon recovery of water potential compared to Q. pubescens which had better night-time recovery. Q. ilex and Q. pubescens exposed to elevated CO2 for prolonged periods exhibit different mechanisms for dealing with additional reduced carbon and do maintain an altered carbon physiology, even in midst of the region’s characteristic summer drought</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>7</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Scarascia-Mugnozza, Giuseppe E</style></author><author><style face="normal" font="default" size="100%">Angelis, Paolo De</style></author><author><style face="normal" font="default" size="100%">Matteucci, Giorgio</style></author><author><style face="normal" font="default" size="100%">Kuzminsky, Elena</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Fakhri A. Bazzaz BT - Carbon Dioxide and Communities, Populations</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">14 - Carbon Metabolism and Plant Growth under Elevated CO2 in a Natural Quercus ilex L. “Macchia” Stand</style></title><secondary-title><style face="normal" font="default" size="100%">Carbon Dioxide, Populations, and Communities</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">acclimation processes (PG)</style></keyword><keyword><style  face="normal" font="default" size="100%">biomass allocation</style></keyword><keyword><style  face="normal" font="default" size="100%">carbon metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">long-term exposure</style></keyword><keyword><style  face="normal" font="default" size="100%">mediterranean macchia</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1996</style></year></dates><publisher><style face="normal" font="default" size="100%">Academic Press</style></publisher><pub-location><style face="normal" font="default" size="100%">San Diego</style></pub-location><pages><style face="normal" font="default" size="100%">209-230</style></pages><isbn><style face="normal" font="default" size="100%">978-0-12-420870-4</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Publisher Summary This chapter examines the impact of long-term exposure to elevated CO2 concentration in a natural Mediterranean community dominated by Quercus ilex (high &quot;macchia&quot;). The research emphasizes on measurements of carbon metabolism and light energy utilization by the leaves to assess the physiological responses that subtend growth rather than just measuring short-term biomass increments at the tree level alone. Given the relevance of the Mediterranean woodland communities from an economical and environmental perspective, it is critical to be able to predict the possible effects of global change on these ecosystems and to eventually adopt adequate mitigation strategies. The interaction between carbon metabolism and biomass partitioning in woody plants is also regulated by nutrient availability. In the nutrient-limited Mediterranean environment, a CO2 increase may in part relieve this limitation by a greater efficiency of nutrient utilization, especially in tree species, characterized by a large proportion of their biomass allocated to components with low nutrient cost. These limitations are likely to moderate the responses of plants and communities to a global change, particularly to increases in atmospheric CO2 and biosphere warming. After a three-year period, the community responses to elevated CO2 indicate a wide range of acclimation processes by tree and shrub species in relation to their different ecological strategies.</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%">FARIA, T.</style></author><author><style face="normal" font="default" size="100%">Wilkins, D.</style></author><author><style face="normal" font="default" size="100%">Besford, R. T.</style></author><author><style face="normal" font="default" size="100%">Vaz, M.</style></author><author><style face="normal" font="default" size="100%">Pereira, J. S.</style></author><author><style face="normal" font="default" size="100%">Chaves, M. M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Growth at elevated CO2 leads to down-regulation of photosynthesis and altered response to high temperature in Quercus suber L. seedlings</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%">acclimation</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">photo- synthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</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://jxb.oxfordjournals.org/content/47/11/1755.abstract</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">1755 - 1761</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The effects of growth at elevated CO2 on the response to high temperatures in terms of carbon assimilation (net photosynthesis, stomatal conductance, amount and activity of Rubisco, and concentrations of total soluble sugars and starch) and of photochemistry (for example, the efficiency of excitation energy captured by open photosystem II reaction centres) were studied in cork oak (Quercus suber L.). Plants grown in elevated CO2 (700 ppm) showed a down-regulation of photosynthesis and had lower amounts and activity of Rubisco than plants grown at ambient CO2 (350 ppm), after 14 months in the greenhouse. At that time plants were subjected to a heat-shock treatment (4 h at 45°C in a chamber with 80% relative humidity and 800–1000 µmol m−2 s−1 photon flux density). Growth in a CO2-enriched atmosphere seems to protect cork oak leaves from the short-term effects of high temperature. Elevated CO2 plants had positive net carbon uptake rates during the heat shock treatment whereas plants grown at ambient CO2 showed negative rates. Moreover, recovery was faster in high CO2-grown plants which, after 30 min at 25°C, exhibited higher net carbon uptake rates and lower decreases in photosynthetic capacity (Amax as well as in the efficiency of excitation energy captured by open photosystem II reaction centres (FvJFm than plants grown at ambient CO2. The stomata of elevated CO2 plants were also less responsive when exposed to high temperature.</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><notes><style face="normal" font="default" size="100%">10.1093/jxb/47.11.175510.1093/jxb/47.11.1755</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%">Faria, T</style></author><author><style face="normal" font="default" size="100%">Wilkins, D</style></author><author><style face="normal" font="default" size="100%">Besford, R T</style></author><author><style face="normal" font="default" size="100%">Vaz, M</style></author><author><style face="normal" font="default" size="100%">Pereira, J S</style></author><author><style face="normal" font="default" size="100%">Chaves, M M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Growth at elevated CO2 leads to down-regulation of photosynthesis and altered response to high temperature in Quercus suber L. seedlings</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%">acclimation</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">photo- synthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1996</style></year></dates><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">1755-1761</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The effects of growth at elevated CO2 on the response to high temperatures in terms of carbon assimilation (net photosynthesis, stomatal conductance, amount and activity of Rubisco, and concentrations of total soluble sugars and starch) and of photochemistry (for example, the efficiency of excitation energy captured by open photosystem II reaction centres) were studied in cork oak (Quercus suber L.). Plants grown in elevated CO2 (700 ppm) showed a down-regulation of photosynthesis and had lower amounts and activity of Rubisco than plants grown at ambient CO2 (350 ppm), after 14 months in the greenhouse. At that time plants were subjected to a heat-shock treatment (4 h at 45°C in a chamber with 80% relative humidity and 800–1000 µmol m−2 s−1 photon flux density). Growth in a CO2-enriched atmosphere seems to protect cork oak leaves from the short-term effects of high temperature. Elevated CO2 plants had positive net carbon uptake rates during the heat shock treatment whereas plants grown at ambient CO2 showed negative rates. Moreover, recovery was faster in high CO2-grown plants which, after 30 min at 25°C, exhibited higher net carbon uptake rates and lower decreases in photosynthetic capacity (Amax as well as in the efficiency of excitation energy captured by open photosystem II reaction centres (FvJFm than plants grown at ambient CO2. The stomata of elevated CO2 plants were also less responsive when exposed to high temperature.</style></abstract><notes><style face="normal" font="default" size="100%">10.1093/jxb/47.11.1755</style></notes><research-notes><style face="normal" font="default" size="100%">10.1093/jxb/47.11.1755</style></research-notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tognetti, R</style></author><author><style face="normal" font="default" size="100%">Giovannelli, A</style></author><author><style face="normal" font="default" size="100%">Longobucco, A</style></author><author><style face="normal" font="default" size="100%">Miglietta, F</style></author><author><style face="normal" font="default" size="100%">Raschi, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Water relations of oak species growing in the natural CO2 spring of Rapolano (central Italy)</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%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">embolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus pubescens</style></keyword><keyword><style  face="normal" font="default" size="100%">sap flow</style></keyword><keyword><style  face="normal" font="default" size="100%">water relations</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1996</style></year></dates><volume><style face="normal" font="default" size="100%">53</style></volume><pages><style face="normal" font="default" size="100%">475-485</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The effect of elevated atmospheric carbon dioxide on water relations was examined on downy oak (Quercus pubescens) and holm oak (Q ilex) trees. The study was conducted on trees growing in a naturally enriched CO2 spring. Sap velocity and sap flow were measured by the heat pulse technique. On the same trees, daily courses of xylem water potential, leaf conductance and transpiration were monitored. Plant water relations were evaluated by pressure-volume analysis method on shoots; on the same branches, relative conductivity of xylem was measured. Both species exhibited increased osmotic potential and decreased symplasmic fraction of water in trees adapted to increased CO2. Downy oak showed lower stomatal conductance under elevated CO2, but holm oak did not. Both species displayed higher sap flow in control trees. In both species, increased carbon dioxide did not influence xylem embolism 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%">Chaves, M. M.</style></author><author><style face="normal" font="default" size="100%">Pereira, J. S.</style></author><author><style face="normal" font="default" size="100%">Cerasoli, S.</style></author><author><style face="normal" font="default" size="100%">CliftonBrown, J.</style></author><author><style face="normal" font="default" size="100%">Miglietta, F.</style></author><author><style face="normal" font="default" size="100%">Raschi, A.</style></author><author><style face="normal" font="default" size="100%">Chaves J. S. ;Cerasoli, S. ;Clifton Brown</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Leaf metabolism during summer drought in Quercus ilex trees with lifetime exposure to elevated CO2</style></title><secondary-title><style face="normal" font="default" size="100%">JOURNAL OF BIOGEOGRAPHY</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Fisiologia - CO2 elevado</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">long-term acclimation</style></keyword><keyword><style  face="normal" font="default" size="100%">stomata</style></keyword><keyword><style  face="normal" font="default" size="100%">sugars</style></keyword><keyword><style  face="normal" font="default" size="100%">water deficits</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1995</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1995///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">&lt;GotoISI&gt;://WOS:A1995TR05500013</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">22</style></volume><pages><style face="normal" font="default" size="100%">255 - 259</style></pages><isbn><style face="normal" font="default" size="100%">0305-0270</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A marginal improvement in the response of Quercus ilex adult trees to drought appears to occur under a long-term natural CO2 enrichment. This is expressed, for example, by the absence of midday stomatal closure in trees growing under elevated CO2. Some protection against high irradiance and high temperature seems also to occur at the photochemical level, presumably as a result of more carbon available to the consumption of excess light energy. This would allow a better performance of the plants grown under elevated CO2 during the warmer hours of the day and therefore playing an important adaptation role under drought conditions. A marginal increase in the concentration of soluble sugars and starch was observed in the leaves of trees growing at elevated CO2 as compared with plants at ambient CO2, mainly during the midday hours. We may speculate that this will be advantageous both in terms of carbohydrate reserves for growth (e.g. more roots) and osmotic adjustment.</style></abstract><issue><style face="normal" font="default" size="100%">02-Mar</style></issue><notes><style face="normal" font="default" size="100%">From Duplicate 2 (Leaf metabolism during summer drought in Quercus ilex trees with lifetime exposure to elevated CO2 - Chaves, M M; Pereira, J S; Cerasoli, S; CliftonBrown, J; Miglietta, F; Raschi, A)From Duplicate 2 (Leaf metabolism during summer drought in Quercus ilex trees with lifetime exposure to elevated CO2 - Chaves, M M; Pereira, J S; Cerasoli, S; CliftonBrown, J; Miglietta, F; Raschi, A)The following values have no corresponding Zotero field:&lt;br/&gt;pub-location: OSNEY MEAD, OXFORD, OXON, ENGLAND OX2 0EL&lt;br/&gt;publisher: BLACKWELL SCIENCE LTD&lt;br/&gt;label: Fisiologia - CO2 elevado</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%">Chaves, M M</style></author><author><style face="normal" font="default" size="100%">Pereira, J S</style></author><author><style face="normal" font="default" size="100%">Cerasoli, S</style></author><author><style face="normal" font="default" size="100%">CliftonBrown, J</style></author><author><style face="normal" font="default" size="100%">Miglietta, F</style></author><author><style face="normal" font="default" size="100%">Raschi, A</style></author><author><style face="normal" font="default" size="100%">Chaves J. S.;Cerasoli,S.;Clifton Brown,J.;Miglietta,F.;Raschi,A., M M ;Pereira</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Leaf metabolism during summer drought in Quercus ilex trees with lifetime exposure to elevated CO2</style></title><secondary-title><style face="normal" font="default" size="100%">JOURNAL OF BIOGEOGRAPHY</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elevated CO2</style></keyword><keyword><style  face="normal" font="default" size="100%">Fisiologia - CO2 elevado</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">long-term acclimation</style></keyword><keyword><style  face="normal" font="default" size="100%">stomata</style></keyword><keyword><style  face="normal" font="default" size="100%">sugars</style></keyword><keyword><style  face="normal" font="default" size="100%">water deficits</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1995</style></year></dates><publisher><style face="normal" font="default" size="100%">BLACKWELL SCIENCE LTD</style></publisher><pub-location><style face="normal" font="default" size="100%">OSNEY MEAD, OXFORD, OXON, ENGLAND OX2 0EL</style></pub-location><volume><style face="normal" font="default" size="100%">22</style></volume><pages><style face="normal" font="default" size="100%">255-259</style></pages><isbn><style face="normal" font="default" size="100%">0305-0270</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A marginal improvement in the response of Quercus ilex adult trees to drought appears to occur under a long-term natural CO2 enrichment. This is expressed, for example, by the absence of midday stomatal closure in trees growing under elevated CO2. Some protection against high irradiance and high temperature seems also to occur at the photochemical level, presumably as a result of more carbon available to the consumption of excess light energy. This would allow a better performance of the plants grown under elevated CO2 during the warmer hours of the day and therefore playing an important adaptation role under drought conditions. A marginal increase in the concentration of soluble sugars and starch was observed in the leaves of trees growing at elevated CO2 as compared with plants at ambient CO2, mainly during the midday hours. We may speculate that this will be advantageous both in terms of carbohydrate reserves for growth (e.g. more roots) and osmotic adjustment.</style></abstract><notes><style face="normal" font="default" size="100%">From Duplicate 2 (Leaf metabolism during summer drought in Quercus ilex trees with lifetime exposure to elevated CO2 - Chaves, M M; Pereira, J S; Cerasoli, S; CliftonBrown, J; Miglietta, F; Raschi, A)</style></notes><research-notes><style face="normal" font="default" size="100%">From Duplicate 2 (Leaf metabolism during summer drought in Quercus ilex trees with lifetime exposure to elevated CO2 - Chaves, M M; Pereira, J S; Cerasoli, S; CliftonBrown, J; Miglietta, F; Raschi, A)</style></research-notes><label><style face="normal" font="default" size="100%">Fisiologia - CO2 elevado</style></label></record></records></xml>