<?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%">García, D</style></author><author><style face="normal" font="default" size="100%">Rodríguez, J</style></author><author><style face="normal" font="default" size="100%">Sanz, J M</style></author><author><style face="normal" font="default" size="100%">Merino, J</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Response of two populations of holm oak (Quercus rotundifolia Lam.) to sulfur dioxide.</style></title><secondary-title><style face="normal" font="default" size="100%">Ecotoxicology and environmental safety</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adaptation</style></keyword><keyword><style  face="normal" font="default" size="100%">Air Pollutants</style></keyword><keyword><style  face="normal" font="default" size="100%">Air Pollutants: adverse effects</style></keyword><keyword><style  face="normal" font="default" size="100%">air pollution</style></keyword><keyword><style  face="normal" font="default" size="100%">biomass</style></keyword><keyword><style  face="normal" font="default" size="100%">Environment</style></keyword><keyword><style  face="normal" font="default" size="100%">GROWTH RATE</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Photosynthesis: physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Physiological</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Pollutants</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus rotundifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulfur Dioxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulfur Dioxide: adverse effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulphur dioxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees: drug effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees: genetics</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees: physiology</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><volume><style face="normal" font="default" size="100%">40</style></volume><pages><style face="normal" font="default" size="100%">42-48</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Experiments were carried out with seedlings of Quercus rotundifolia Lam., an evergreen schlerophyllous tree typical of the Spanish Mediterranean climate environments. Fruits were collected in two distant (800 km) populations located in the center (southern Spain) and northern border (northern Spain) of the area of distribution of the species. One-month-old potted plants were grown for 130 days in an enriched atmosphere of SO2 (0.23 ppm, 14 h/day) in controlled (growth chamber) conditions. Both northern and southern plants underwent a significant decrease in growth rate as a consequence of the treatment. Even so, plants appear to be quite resistant to SO2 compared with either more temperate or more productive species. The southern population was more sensitive to the treatment, as reflected by the bigger decrease in both growth and photosynthetic rates. Differences in resistance appear to be related to the biogeographic origin of the populations studied, which underlines the importance of biogeographic aspects in studies of resistance to air pollutants.</style></abstract><accession-num><style face="normal" font="default" size="100%">9626534</style></accession-num></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%">García, D.</style></author><author><style face="normal" font="default" size="100%">Rodríguez, J.</style></author><author><style face="normal" font="default" size="100%">Sanz, J. M.</style></author><author><style face="normal" font="default" size="100%">Merino, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Response of two populations of holm oak (Quercus rotundifolia Lam.) to sulfur dioxide.</style></title><secondary-title><style face="normal" font="default" size="100%">Ecotoxicology and environmental safety</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adaptation</style></keyword><keyword><style  face="normal" font="default" size="100%">Air Pollutants</style></keyword><keyword><style  face="normal" font="default" size="100%">Air Pollutants: adverse effects</style></keyword><keyword><style  face="normal" font="default" size="100%">air pollution</style></keyword><keyword><style  face="normal" font="default" size="100%">biomass</style></keyword><keyword><style  face="normal" font="default" size="100%">Environment</style></keyword><keyword><style  face="normal" font="default" size="100%">GROWTH RATE</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Photosynthesis: physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Physiological</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Pollutants</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus rotundifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulfur Dioxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulfur Dioxide: adverse effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Sulphur dioxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees: drug effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees: genetics</style></keyword><keyword><style  face="normal" font="default" size="100%">Trees: physiology</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.ncbi.nlm.nih.gov/pubmed/9626534</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">40</style></volume><pages><style face="normal" font="default" size="100%">42 - 48</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Experiments were carried out with seedlings of Quercus rotundifolia Lam., an evergreen schlerophyllous tree typical of the Spanish Mediterranean climate environments. Fruits were collected in two distant (800 km) populations located in the center (southern Spain) and northern border (northern Spain) of the area of distribution of the species. One-month-old potted plants were grown for 130 days in an enriched atmosphere of SO2 (0.23 ppm, 14 h/day) in controlled (growth chamber) conditions. Both northern and southern plants underwent a significant decrease in growth rate as a consequence of the treatment. Even so, plants appear to be quite resistant to SO2 compared with either more temperate or more productive species. The southern population was more sensitive to the treatment, as reflected by the bigger decrease in both growth and photosynthetic rates. Differences in resistance appear to be related to the biogeographic origin of the populations studied, which underlines the importance of biogeographic aspects in studies of resistance to air pollutants.</style></abstract><issue><style face="normal" font="default" size="100%">1-2</style></issue><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;accession-num: 9626534</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%">Kesselmeier, J</style></author><author><style face="normal" font="default" size="100%">Bode, K</style></author><author><style face="normal" font="default" size="100%">Hofmann, U</style></author><author><style face="normal" font="default" size="100%">Mtjller, H</style></author><author><style face="normal" font="default" size="100%">Schafer, L</style></author><author><style face="normal" font="default" size="100%">Wolf, A</style></author><author><style face="normal" font="default" size="100%">Ciccioli, P</style></author><author><style face="normal" font="default" size="100%">Cecinato, A</style></author><author><style face="normal" font="default" size="100%">Frattoni, M</style></author><author><style face="normal" font="default" size="100%">Foster, P</style></author><author><style face="normal" font="default" size="100%">Dutaur, L</style></author><author><style face="normal" font="default" size="100%">Torreq, L</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">EMISSION OF SHORT CHAINED ORGANIC ACIDS , ALDEHYDES AND MONOTERPENES FROM QUERCUS ILEX L . AND PINUS PINEA L . IN RELATION TO PHYSIOLOGICAL ACTIVITIES , CARBON BUDGET AND EMISSION ALGORITHMS</style></title><secondary-title><style face="normal" font="default" size="100%">Atmospheric Environment</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">aldehydes</style></keyword><keyword><style  face="normal" font="default" size="100%">carbon budget</style></keyword><keyword><style  face="normal" font="default" size="100%">coniferous</style></keyword><keyword><style  face="normal" font="default" size="100%">deciduous</style></keyword><keyword><style  face="normal" font="default" size="100%">light</style></keyword><keyword><style  face="normal" font="default" size="100%">Monoterpenes</style></keyword><keyword><style  face="normal" font="default" size="100%">oak</style></keyword><keyword><style  face="normal" font="default" size="100%">organic acids</style></keyword><keyword><style  face="normal" font="default" size="100%">pine</style></keyword><keyword><style  face="normal" font="default" size="100%">Pinus pinea L</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex L</style></keyword><keyword><style  face="normal" font="default" size="100%">Temperature</style></keyword><keyword><style  face="normal" font="default" size="100%">Volatile Organic Compounds</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1997</style></year></dates><volume><style face="normal" font="default" size="100%">31</style></volume><pages><style face="normal" font="default" size="100%">119-133</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">We report on the emission of monoterpenes, short-chained organic acids and aldehydes from Mediterranean oak (Quercus ilex L.) and pine (Pinus pinea L.). All studies were done with dynamic cuvettes enclosing intact branches at the top of the canopy flushed with ambient air. Daily trends are compared with the photosynthetic active radiation (PAR), leaf temperature and the physiological activities of the enclosed branches, i.e. assimilation and transpiration, with special attention on the carbon budget. Oak emits monoterpenes in high amounts, up to 2% of the assimilated carbon. As compared with monoterpenes, short-chained organic acids and aldehydes are of minor importance for oak. However, on a leaf dry-weight basis equal amounts of acids and aldehydes are released from oak and pine. As pine emitted only low amounts of terpenes (below 0.2% of the assimilated carbon) the release of terpenes and oxygenated compounds is of equal importance for this species. A comparison of a modelled light and temperature driven emission with the observed volatile organic compounds (VOC) emissions showed good agreement for monoterpenes as well as for organic acids emitted in the case of oak. For pine only the release of acids showed an adequate relation to the algorithm data, whereas the terpene emissions seemed to be dominated by temperature effects</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%">Kesselmeier, J</style></author><author><style face="normal" font="default" size="100%">Fer, L S C H</style></author><author><style face="normal" font="default" size="100%">Ciccioli, P</style></author><author><style face="normal" font="default" size="100%">Brancaleoni, E</style></author><author><style face="normal" font="default" size="100%">Cecinato, A</style></author><author><style face="normal" font="default" size="100%">Frattoni, M</style></author><author><style face="normal" font="default" size="100%">Foster, I P</style></author><author><style face="normal" font="default" size="100%">Jacob, V</style></author><author><style face="normal" font="default" size="100%">Denis, J</style></author><author><style face="normal" font="default" size="100%">Fugit, J L</style></author><author><style face="normal" font="default" size="100%">Dutaur, L</style></author><author><style face="normal" font="default" size="100%">Torres, L</style></author><author><style face="normal" font="default" size="100%">Mainz, D-</style></author><author><style face="normal" font="default" size="100%">Salaria, Via</style></author><author><style face="normal" font="default" size="100%">Scalo, Monterotondo</style></author><author><style face="normal" font="default" size="100%">De, Institut Universitaire</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">EMISSION OF MONOTERPENES AND ISOPRENE FROM A MEDITERRANEAN OAK SPECIES QUERCUS ILEX L. MEASURED WITHIN THE BEMA (BIOGENIC EMISSIONS IN THE MEDITERRANEAN AREA) PROJECT EMISSIONS IN THE M E D I T E</style></title><secondary-title><style face="normal" font="default" size="100%">Atmospheric Environment</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biogenic emission</style></keyword><keyword><style  face="normal" font="default" size="100%">isoprene</style></keyword><keyword><style  face="normal" font="default" size="100%">light</style></keyword><keyword><style  face="normal" font="default" size="100%">Monoterpenes</style></keyword><keyword><style  face="normal" font="default" size="100%">non-methane hydrocarbons</style></keyword><keyword><style  face="normal" font="default" size="100%">oak</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">VOC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1996</style></year></dates><volume><style face="normal" font="default" size="100%">30</style></volume><pages><style face="normal" font="default" size="100%">1841-1850</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">We report on some results of our studies of monoterpene and isoprene emissions and the physiological activities of an oak species (Quercus ilex L.) under the Mediterranean climatic conditions found at Castel Porziano (Rome) in June 1993. The oak species Quercus ilex L. was found to emit mainly monoterpenes in high amounts. Isoprene emissions were negligible. Diel cycles of monoterpene emissions showed correlation with light and the diel behaviour of photosynthetic CO2 assimilation, transpiration and stomatal corductance. Temperature dependence seemed to be of minor importance.</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%">VIGNES, D</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">GASEOUS EXCHANGES AND THEIR REGULATION IN 2 SPECIES OF EVERGREEN OAK (QUERCUS ILEX AND QUERCUS SUBER)</style></title><secondary-title><style face="normal" font="default" size="100%">BULLETIN DE LA SOCIETE BOTANIQUE DE FRANCE-ACTUALITES BOTANIQUES</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">hydric potential</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthetic production</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant physiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal conductance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1988</style></year></dates><publisher><style face="normal" font="default" size="100%">SOC BOTANIQUE FRANCE</style></publisher><pub-location><style face="normal" font="default" size="100%">RUE J B CLEMENT, 92296 CHATENAY-MALABRY CEDEX, FRANCE</style></pub-location><volume><style face="normal" font="default" size="100%">135</style></volume><pages><style face="normal" font="default" size="100%">99-108</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">This article presents a comparison on the physiology (hyrdic potential, stomatal resistances, transpiration, net photosynthesis) of young plants of Quercus ilex and Quercus suber submitted to different temperatures, light environment and water supply. Relative to temperature and light, the two species present similar reactions, although gaseous exchanges are more important on Quercus ilex. On the contrary, they present distinctive differences on water absorption. Quercus ilex have an important transpiration when water supply is not limited, but presents also a good tolerance to low hydric potentials and sufficient stomatal conductance according to photosynthetic production. On Quercus suber, survival seems more important than production : water consumption is relatively reduced at high water potential as good as at low water potential.</style></abstract><notes><style face="normal" font="default" size="100%">APS</style></notes><research-notes><style face="normal" font="default" size="100%">APS</style></research-notes></record></records></xml>