<?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%">Kaplan, Hatice Coelgecen Ayse</style></author><author><style face="normal" font="default" size="100%">Buyukkartal, H Nurhan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">CALCIUM OXALATE CRYSTALS IN LEAVES OF QUERCUS CERRIS L. AND Q-ILEX L.</style></title><secondary-title><style face="normal" font="default" size="100%">BANGLADESH JOURNAL OF BOTANY</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calcium oxalate crystals</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><publisher><style face="normal" font="default" size="100%">BANGLADESH BOTANICAL SOC</style></publisher><pub-location><style face="normal" font="default" size="100%">UNIV DACCA DEPT BOTANY, 2 DHAKA, BANGLADESH</style></pub-location><volume><style face="normal" font="default" size="100%">38</style></volume><pages><style face="normal" font="default" size="100%">103-105</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Leaves of Quercus cerris L. were collected from Zonguldak, Devrek and those of Q. ilex L. samples were collected from Zonguldak, Eregli, Turkey. The leaf sections were subjected to histochemical analysis and brown-black stained calcium oxalate crystals were identified. The organic contents in the leaves were completely cleaned for polarizing microscope investigation. Calcium oxalate crystals were found to be druz and prismatic in Q. cerris and Q. ilex species. While druz crystals were localized in mesophyll, prismatic ones were localized around the leaf vessels. The amount of calcium oxalate crystals per mm(2) was determined in permanent preparations.</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%">Gratani, L</style></author><author><style face="normal" font="default" size="100%">Bonito, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Leaf traits variation during leaf expansion in Quercus ilex L.</style></title><secondary-title><style face="normal" font="default" size="100%">Photosynthetica</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf expansion</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf morphology</style></keyword><keyword><style  face="normal" font="default" size="100%">net photosynthetic rate</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">323-330</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The morphological, anatomical and physiological variations of leaf traits were analysed during Quercus ilex L. leaf expansion. The leaf water content (LWC), leaf area relative growth rate (RGRl ) and leaf dry mass relative growth rate (RGRm) were the highest (76±2 %, 0.413 cm 2 cm –2 d –1 , 0.709 mg mg –1 d –1 , respectively) at the beginning of the leaf expansion process (7 days after bud break). Leaf expansion lasted 84±2 days when air temperature ranged from 13.3±0.8 to 27.6±0.9 °C. The net photosynthetic rate (PN), stomatal conductance (gs ), and chlorophyll content per fresh mass (Chl) increased during leaf expansion, having the highest values [12.62±1.64 µmol (CO2) m –2 s –1 , 0.090 mol (H2O) m –2 s –1 , and 1.03±0.08 mg g –1 ,respectively] 56 days after bud break. Chl was directly correlated with leaf dry mass (DM) and PN. The thickness of palisade parenchyma contributed to the total leaf thickness (263.1±1.5 μm) by 47 %, spongy layer thickness 38 %, adaxial epidermis and cuticle thickness 9 %, and abaxial epidermis and cuticle thickness 6 %. Variation in leaf size during leaf expansion might be attributed to a combination of cells density and length, and it is confirmed by the significant (p&lt;0.001) correlations among these traits. Q. ilex leaves reached 90 % of their definitive structure before the most severe drought period (beginning of June – end of August). The high leaf mass area (LMA, 15.1±0.6 mg cm –2 ) at full leaf expansion was indicative of compact leaves (2028±100 cells mm –2 ). Air temperature increasing might shorten the favourable period for leaf expansion, thus changing the final amount of biomass per unit leaf area 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%">GRATANI, L.</style></author><author><style face="normal" font="default" size="100%">Bonito, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Leaf traits variation during leaf expansion in Quercus ilex L.</style></title><secondary-title><style face="normal" font="default" size="100%">Photosynthetica</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf expansion</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf morphology</style></keyword><keyword><style  face="normal" font="default" size="100%">net photosynthetic rate</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2009///</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/index/J6N552465N18M216.pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">323 - 330</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The morphological, anatomical and physiological variations of leaf traits were analysed during Quercus ilex L. leaf expansion. The leaf water content (LWC), leaf area relative growth rate (RGRl ) and leaf dry mass relative growth rate (RGRm) were the highest (76±2 %, 0.413 cm 2 cm –2 d –1 , 0.709 mg mg –1 d –1 , respectively) at the beginning of the leaf expansion process (7 days after bud break). Leaf expansion lasted 84±2 days when air temperature ranged from 13.3±0.8 to 27.6±0.9 °C. The net photosynthetic rate (PN), stomatal conductance (gs ), and chlorophyll content per fresh mass (Chl) increased during leaf expansion, having the highest values [12.62±1.64 µmol (CO2) m –2 s –1 , 0.090 mol (H2O) m –2 s –1 , and 1.03±0.08 mg g –1 ,respectively] 56 days after bud break. Chl was directly correlated with leaf dry mass (DM) and PN. The thickness of palisade parenchyma contributed to the total leaf thickness (263.1±1.5 μm) by 47 %, spongy layer thickness 38 %, adaxial epidermis and cuticle thickness 9 %, and abaxial epidermis and cuticle thickness 6 %. Variation in leaf size during leaf expansion might be attributed to a combination of cells density and length, and it is confirmed by the significant (p&lt;0.001) correlations among these traits. Q. ilex leaves reached 90 % of their definitive structure before the most severe drought period (beginning of June – end of August). The high leaf mass area (LMA, 15.1±0.6 mg cm –2 ) at full leaf expansion was indicative of compact leaves (2028±100 cells mm –2 ). Air temperature increasing might shorten the favourable period for leaf expansion, thus changing the final amount of biomass per unit leaf area of Q. ilex.</style></abstract><issue><style face="normal" font="default" size="100%">3</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%">Lersten, N. R.</style></author><author><style face="normal" font="default" size="100%">Horner, Harry T.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Crystal macropatterns in leaves of Fagaceae and Nothofagaceae: a comparative study</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Systematics and Evolution</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calcium oxalate</style></keyword><keyword><style  face="normal" font="default" size="100%">crystals</style></keyword><keyword><style  face="normal" font="default" size="100%">Fagaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">macropatterns</style></keyword><keyword><style  face="normal" font="default" size="100%">Nothofagaceae</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://www.springerlink.com/index/10.1007/s00606-007-0620-4</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">271</style></volume><pages><style face="normal" font="default" size="100%">239 - 253</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Crystal macropatterns in Fagaceae and Nothofagaceae were examined from cleared herbarium leaves (eight genera, 122 spp.) by polarizing microscopy. Prisms and druses dominate, but previously undescribed intermediate forms occur in 25 species of Fagaceae. Sixty-two species had only prisms associated with vein orders 1–4, but smallest orders 5 and 6 had few or no crystals. In mesophyll, 98 species had small druses in spongy parenchyma and larger but fewer druses in palisade parenchyma. Subfamily Fagoideae conformed closely to this macropattern, Castaneoideae less so. Six Castaneoideae species lacked vein crystals. Two Fagoideae species and seven Nothofagus species lacked mesophyll crystals. Druses with prominent cores occur throughout Fagaceae but none were seen in Nothofagaceae. Tabular presentation of results shows signiﬁcant although overlapping trends from Fagoideae to Castaneoideae to Nothofagaceae, with the latter taxon deviating most from Fagaceae.</style></abstract><issue><style face="normal" font="default" size="100%">3-4</style></issue></record></records></xml>