<?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%">Ramírez-Valiente, J. a</style></author><author><style face="normal" font="default" size="100%">Lorenzo, Z.</style></author><author><style face="normal" font="default" size="100%">Soto, A.</style></author><author><style face="normal" font="default" size="100%">Valladares, F.</style></author><author><style face="normal" font="default" size="100%">Gil, L.</style></author><author><style face="normal" font="default" size="100%">Aranda, I.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Natural selection on cork oak: allele frequency reveals divergent selection in cork oak populations along a temperature cline</style></title><secondary-title><style face="normal" font="default" size="100%">Evolutionary Ecology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adaptation</style></keyword><keyword><style  face="normal" font="default" size="100%">Additive effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Dominance</style></keyword><keyword><style  face="normal" font="default" size="100%">Natural selection</style></keyword><keyword><style  face="normal" font="default" size="100%">Overdominance</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2010///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/10.1007/s10682-010-9365-6</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">24</style></volume><pages><style face="normal" font="default" size="100%">1031 - 1044</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A recent study of population divergence at neutral markers and adaptive traits in cork oak has observed an association between genetic distances at locus QpZAG46 and genetic distances for leaf size and growth. In that study it was proposed that certain loci could be linked to genes encoding for adaptive traits in cork oak and, thus, could be used in adaptation studies. In order to investigate this hypothesis, here we (1) looked for associations between molecular markers and a set of adaptive traits in cork oak, and (2) explored the effects of the climate on among-population patterns in adaptive traits and molecular markers. For this purpose, we chose 9-year-old plants originating from thirteen populations spanning a broad range of climatic conditions. Plants established in a common garden site were genotyped at six nuclear microsatellites and phenotypically characterized for six functional traits potentially related to plant performance. Our results supported the proposed linkage between locus QpZAG46 and genes encoding for leaf size and growth. Temperature caused adaptive population divergence in leaf size and growth, which was expressed as differences in the frequencies of the alleles at locus QpZAG46.</style></abstract><issue><style face="normal" font="default" size="100%">5</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%">Aranda, I.</style></author><author><style face="normal" font="default" size="100%">Simón, J. Puértolas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Elevated atmospheric CO2 does not modify osmotic adjustment to light and drought in the Mediterranean oak&quot; Quercus suber L.&quot;</style></title><secondary-title><style face="normal" font="default" size="100%">Investigación agraria. Sistemas y recursos forestales</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CO2 enrichment</style></keyword><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">PV curves</style></keyword><keyword><style  face="normal" font="default" size="100%">shade</style></keyword><keyword><style  face="normal" font="default" size="100%">Water availability</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://dialnet.unirioja.es/servlet/dcart?info=link&amp;codigo=2591523&amp;orden=194238</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">3 - 9</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The current ongoing increase in the atmospheric CO2 concentration is an unquestionable fact. Thus, plants are bound to live in a more enriched CO2 world in a not far-off future. In this new framework, regeneration of forest tree species may be modified as a consequence of the change in the current patterns of seedling response to other environmental resources, such as water or light. We studied the impact of an elevated CO2 concentration on the interaction of drought and light upon the water relations of cork oak (Quercus suber L.) seedlings. In a complete factorial design of contrasting light (HL vs LL), water (WW vs S) and CO2 levels (800 ppm vs 370 ppm), we analysed the influence of each factor and its interaction in the modification of different leaf water parameters in potted seedlings after a 6 months experimental period. These parameters were derived from the construction, with leaf materials, of the P-V curves: osmotic potential at full turgor (Ψπ100), osmotic potential at zero turgor (Ψπ0), modulus of elasticity at full turgor (εmax), and the ratio dry/turgor weight (DW/TW). Doubling of the CO2 levels over the current concentration (380 ppm) did not change any of the studied leaf water parameters, while light and water availabilities had a significant influence. This result does not exclude changes in other basic physiological parameters that could modify the pattern of cork oak regeneration responding to a CO2 enriched atmosphere in the future, and under climatic conditions different to the current ones</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aranda, I.</style></author><author><style face="normal" font="default" size="100%">Castro, L.</style></author><author><style face="normal" font="default" size="100%">Pardos, M.</style></author><author><style face="normal" font="default" size="100%">Gil, L.</style></author><author><style face="normal" font="default" size="100%">Pardos, J. a</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of the interaction between drought and shade on water relations, gas exchange and morphological traits in cork oak (Quercus suber L.) seedlings</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">Drought</style></keyword><keyword><style  face="normal" font="default" size="100%">light</style></keyword><keyword><style  face="normal" font="default" size="100%">osmotic adjustment</style></keyword><keyword><style  face="normal" font="default" size="100%">photosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">water use efficiency</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2005///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S037811270500085X</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">210</style></volume><pages><style face="normal" font="default" size="100%">117 - 129</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The combined effect of drought and light on different physiological and biochemical traits was assessed in cork oak (Quercus suber L.) seedlings grown under two levels of light availability and submitted to a long-standing drought. Watering was withdrawn after germination and seedlings were allowed to dry to a water content of ca. 50% of ﬁeld capacity. At this point, water-stressed seedlings were grown under moderate drought and two light regimes: high light (HL—50%) and low light (LL— 2%). Soil water in control plants was kept close to ﬁeld capacity (90–100%) for both light environments. Water-relations parameters derived from P–V curves, gas exchange and water status at predawn (Cpd ) were evaluated at twice during the experiment. Nitrogen and chlorophyll contents were determined in the same leaves used for the gas exchange measurements. In addition, maximum rate of carboxylation (Vcmax) and electronic transport (Jmax) were derived from A–Ci curves in well-watered seedlings. The variation on moisture availability during the experiment was the same under both light environments. In control plants, Cpd was over 0.3 MPa at the two harvests, while stressed seedlings decreased to 0.9 MPa, with no differences between light treatments. Water stress decreased osmotic potentials at full (Cp100 ) and zero turgor (Cp0 ). The regressions between both potentials and Cpd showed a higher intercept in shade grown seedlings. This fact will point out the higher osmoregulation capacity in sun seedlings whatever water availability. Nitrogen investment on a per leaf mass (Nmass ), chlorophyll content (Chlmass ) and SLA tended to show a typical pattern of sun-shade acclimation. Thus, the three parameters increased with shade. Only for Nmass there was a signiﬁcant effect of watering, since water stress increased Nmass . LL plants showed a lower photosynthetic capacity in terms of maximum net photosynthesis at saturating light (Amax), which was related to a decrease in Vcmax and Jmax . Both parameters varied with speciﬁc leaf area (SLA) in a similar way. The low-light environment brought about a higher nitrogen investment in chlorophyll, while under high-light environment the investment was higher in carboxylation (Vcmax) and electronic transport ( Fmax). Stomatal conductance to water vapour (gwv ) and Amax were lower in low-light seedlings independently of watering. In addition, there was a trend to keep higher intrinsic water use efﬁciency (IWUE) under high light environment. The increase of IWUE under water stress was higher in HL seedlings. This was as consequence of the steeper decline in gwv as Cpd decreased. The decrease of Amax with Cpd occurred in a similar way in LL and HL seedlings. Thus, the HL seedlings tended to sustain a higher ability to increase IWUE than LL seedlings when they were submitted to the same water stress.</style></abstract><issue><style face="normal" font="default" size="100%">1-3</style></issue></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%">Castro, L.</style></author><author><style face="normal" font="default" size="100%">Aranda, I.</style></author><author><style face="normal" font="default" size="100%">Gil, L.</style></author><author><style face="normal" font="default" size="100%">Pardos, J. A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Relaciones hídricas en procedencias de QUERCUS SUBER L.</style></title><secondary-title><style face="normal" font="default" size="100%">III Congreso Forestal Español Congreso</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">osmotic adjustment</style></keyword><keyword><style  face="normal" font="default" size="100%">pressure-volume curves</style></keyword><keyword><style  face="normal" font="default" size="100%">water potential</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><pages><style face="normal" font="default" size="100%">0 - 5</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Response to drought was studied in 5 provenances of cork oak, which are representative of the ecogeographic range of the species. The variation of several water parameters was analysed in 2000 from the beginning of the summer to the first rainy period. Predawn water potential (ψama) was measured on 5 dates on 6 plants per provenance. On the same plants, pressure-volume curves were carried out on twigs from the spring flushing. Several parameters related to responses to drought were estimated: osmotic potential at full turgor (ψπ 100) and at the loss turgor point (ψπ 0), relative water content at zero turgor (CHR0) and elastic modulus at maximum turgor (εmax). Afterwards osmotic and elastic adjustments were evaluated, and the response to drought was separated of the influence of other factor such as phenology. When the water parameters were analysed, there were not significant differences among provenances, meanwhile the differences among dates were highly significant. A decrease in ψπ 100 and an increase of tissue rigidity (εmax) were observed during the period of water stress. The response to drought overlapped with variations due to ontogenic factors.</style></abstract><notes><style face="normal" font="default" size="100%">The following values have no corresponding Zotero field:&lt;br/&gt;periodical: III Congreso Forestal Español Congreso</style></notes></record></records></xml>