<?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%">Guidi, Lucia</style></author><author><style face="normal" font="default" size="100%">Calatayud, Angeles</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Non-invasive tools to estimate stress-induced changes in photosynthetic performance in plants inhabiting Mediterranean areas</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%">Abiotic stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Chlorophyll a fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">climate change</style></keyword><keyword><style  face="normal" font="default" size="100%">Gas exchange</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2013///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.envexpbot.2013.12.007http://www.sciencedirect.com/science/article/pii/S0098847213002189</style></url></web-urls></urls><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In Mediterranean areas, plants are concomitantly exposed to various abiotic stresses such as light intensity, water deficit, extremes in air temperature, air pollutants, etc. These environmental pressures adversely affect plant development. Changes in photosystem activity are an early response of plants to abiotic stresses. Therefore, chlorophyll (Chl) fluorescence and gas exchange, two non-invasive, rapid and inexpensive techniques for measuring photosynthesis in leaves, have been widely used by plant ecophysiologists to analyse plant responses to stressful conditions. Chl a fluorescence and gas exchange parameters can be indeed used to evaluate changes in photochemical and non-photochemical processes in photosystems associated with electron transport, CO2 fixation, and heat dissipation. In this review, we focus our analysis on the effects of different abiotic stresses on the photochemistry of Mediterranean plants using Chl a fluorescence and gas exchange measurements. Since changes in photosynthetic parameters are observed in the absence of visual injuries, these methodologies constitute fundamental tools to predict and evaluate the extent to which abiotic stresses damage photosynthesis.</style></abstract><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;publisher: Elsevier B.V.</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%">Andivia, Enrique</style></author><author><style face="normal" font="default" size="100%">Márquez-García, Belén</style></author><author><style face="normal" font="default" size="100%">VÁZQUEZ-PIQUÉ, JAVIER</style></author><author><style face="normal" font="default" size="100%">Córdoba, Francisco</style></author><author><style face="normal" font="default" size="100%">FERNÁNDEZ, MANUEL</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Autumn fertilization with nitrogen improves nutritional status, cold hardiness and the oxidative stress response of Holm oak (Quercus ilex ssp. ballota [Desf.] Samp) nursery seedlings</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%">Frost tolerance</style></keyword><keyword><style  face="normal" font="default" size="100%">Holm oak</style></keyword><keyword><style  face="normal" font="default" size="100%">Mineral nutrients</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">water stress</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2011///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/10.1007/s00468-011-0593-3</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">26</style></volume><pages><style face="normal" font="default" size="100%">311 - 320</style></pages><isbn><style face="normal" font="default" size="100%">0046801105933</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Holm oak (Quercus ilex ssp. ballota [Desf.] Samp) is one of the most important species in forest communities of the western Mediterranean Basin, but is very vulnerable to environmental stress during the ﬁrst years of its life. In particular, summer drought and winter frosts limit the distribution, survival, and growth of Holm oak. These two stress factors can lead to plasmolysis and/or oxidative stress. We hypothesized that autumn fertilization with nitrogen (N) can improve plant tolerance to these abiotic stress factors and improve plant quality and therefore reforestation success. A 12-week autumn application of 30 or 60 mg N (plus 70 mg N applied to both treatments during the previous 28 weeks in the nursery, i.e. 100 and 130 mg N in total, respectively) improved overall growth, root growth capacity, frost tolerance, and nutritional status of plants relative to plants given 0.0 and 1.5 mg autumnal N, and had no negative effect on seedling response to water stress. A very small increment in N doses during the autumn (1.5 vs. 0.0 mg N) improved some morphological parameters, such as stem diameter (D) and shoot dry weight, and physiological parameters, such as total antioxidant activity. The highest autumnal N dose (60 mg) increased leaf nutrient content without decreasing the concentration, but had a tendency to reduce frost tolerance relative to seedlings given a lower autumnal N dose (30 mg).</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record></records></xml>