<?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%">Daas, C</style></author><author><style face="normal" font="default" size="100%">Montpied, P</style></author><author><style face="normal" font="default" size="100%">Hanchi, B</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%">Responses of photosynthesis to high temperatures in oak saplings assessed by chlorophyll-a fluorescence: inter-specific diversity and temperature-induced plasticity</style></title><secondary-title><style face="normal" font="default" size="100%">Annals of forest science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">optimal temperature</style></keyword><keyword><style  face="normal" font="default" size="100%">Photochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">quantum yield</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus canariensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus coccifera</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus petraea</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus robur</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">65</style></volume><pages><style face="normal" font="default" size="100%">305</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">• The sensitivity of photosynthesis to high temperature was investigated in greenhouse-grown saplings of three Mediterranean (Quercus canariensis Willd., Q. coccifera L. and Q. suber L.) and two temperate European oak species (Q. robur L. and Q. petraea Matt. Liebl.). The sensitivity to high temperature was inferred from F0T curves producing the critical temperature (Tc ) at which a rapid rise in ground chlorophyll a ﬂuorescence (F0) occurs. Tc is known to acclimate to moderately increased ambient temperature by displaying signiﬁcant increases. • We ﬁrst checked whether acclimation of Tc was paralleled by an increase in optimal temperature for light driven electron ﬂux (Topt ,), recorded by measuring quantum yield of photochemistry under saturating CO2 and moderate irradiance. Saplings of Q. suber and Q. canariensis were submitted to four, ﬁve days long ambient temperature steps (15, 25, 35 and 15 ◦ C again). Tc was usually largely above 45 ◦ C while Topt was around 30–35 ◦ C. Both increased with ambient temperature in the two species, and decreased again when temperature returned to the initial values. This recovery was nevertheless not complete after a week at 15 ◦ C. • A second experiment tested whether the plasticity of Tc was of the same extent in the ﬁve species. A signiﬁcant increase of Tc followed by a decrease was detected in all species. Only small inter-speciﬁc diﬀerences were detected in Tc , and temperature induced plasticity was similar in the diﬀerent species: Tc increased by about 4–5 ◦ C while ambient temperature was increased from 15 to 35 ◦ C. Mediterranean and European oaks did not diﬀer in this respect. • This result does not support the hypothesis that oak species from warmer regions would display a larger plasticity of Tc in response to increasing temperatures.</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></dates><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></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%">Epron, D</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%">Stomatal and non stomatal limitation of photosynthesis by leaf water deficits in three oak species: a comparison of gas exchange and chlorophyll a fluorescence data</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 a fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">oak</style></keyword><keyword><style  face="normal" font="default" size="100%">photoinhibition</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%">water stress</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1990</style></year></dates><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">435-450</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Net CO2 assimilation (A), stomatal conductance for CO2 (g), intercellular mole fraction of CO2 (Ci), kinetics of chlorophyll a fluorescence, and their half decay time (t1/2), their ratio of fluorescence decrease (Rfd), and their adaptive index (Ap) have been monitored on potted trees from 3 oak species (Quercus petraea, Q pubescens and Q ilex) grown in a climate chamber and submitted to drought. Use of A vs Ci representations for photosynthesis data revealed an apparent impairment of mesophyll photosynthesis, together with reduced CO2 supply to mesophyll due to stomatal closure. But in all species chlorophyll a fluorescence kinetics displayed very similar shapes, constant t1/2 and stable Rfd and Ap values until predawn leaf water potential dropped below -4.0 MPa. These observations led to the conclusion that photochemical energy conversion and photosynthetic carbon reduction cycle could be very resistant to leaf water deficits, and that observed decreases in mesophyll photosynthesis had to be attributed to a possible artefact in Ci calculation. On the other hand, the susceptibility of leaves to photoinhibition increased as a consequence of water shortage, especially in Q petraea and Q pubescens. Differences in drought adaptation between the studied species could probably be related to susceptibility to photoinhibition rather than to a direct sensitivity of photosynthesis to leaf water deficits, at least in the range of stress intensities of ecophysiological significance.</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%">Dreyer, E</style></author><author><style face="normal" font="default" size="100%">Bousquet, F</style></author><author><style face="normal" font="default" size="100%">Ducrey, M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Use of pressure volume curves in water relation analysis on woody shoots: influence of rehydration and comparison of four European oak species</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%">pressure-volume curve</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus sp</style></keyword><keyword><style  face="normal" font="default" size="100%">turgor</style></keyword><keyword><style  face="normal" font="default" size="100%">water potential</style></keyword><keyword><style  face="normal" font="default" size="100%">water relations</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1990</style></year></dates><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">285-297</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Pressure volume analyses were undertaken on leafy shoots of 4 European oak species (Quercus robur, Q petraea, Q pubescens and Q ilex) in order to determine the relationship between leaf water potential, average osmotic potential and volume averaged turgor. Some technical limitations of pressure volume analysis, as shown by the influence of the resaturation method on computed turgor, were overcome by accounting for losses of intercellular water during the first stages of dehydration. Variations in leaf to stem ratio, which are very important between large leaved oaks and small leaved evergreens, surprisingly did not influence the relative symplasmic volume of our samples. Differences in mean osmotic potential at full turgor (&amp;Pi0) were related to species, with higher values in drought adapted species, and to leaf age and growing conditions. Values of volumetric modulus of elasticity (ε o) did not significantly influence the relations between leaf water potential (Ψw) and turgor (P) in different species. This relationship was mostly related to &amp;Pi0. Finally, tolerance to drought appeared to be related more to the ability to osmotically adjust in response to changes in environment rather than to the absolute values of &amp;Pi0.</style></abstract></record></records></xml>