Quercus dentata: Carrero, C.

Author(s):  
Keyword(s):  
2005 ◽  
Vol 250 (3-4) ◽  
pp. 231-242 ◽  
Author(s):  
M. Y. Chung ◽  
K.-J. Kim ◽  
J.-H. Pak ◽  
C.-W. Park ◽  
B.-Y. Sun ◽  
...  

2004 ◽  
Vol 34 (12) ◽  
pp. 2501-2507 ◽  
Author(s):  
Takahide A Ishida ◽  
Kouhei Hattori ◽  
Masahito T Kimura

We examined responses of phytophagous insects to hybrids between Quercus crispula Blume and Quercus dentata Thunberg in a natural population in northern Japan. The abundance of leafminers and leaf area loss by chewing insects in hybrids were intermediate between those in the parental species (additive mode), close to those of either of the parental species (dominance mode), or similar to those of both parental species (no difference). Hybrids were neither more susceptible nor resistant to the insect herbivores we monitored. In Phyllonorycter (Gracillariidae) species, which are specialized to either of the parental oak species, the mortality of sap-feeding early instar larvae did not differ between hybrids and the parental species. The abundance of four leafminer taxa was correlated with environmental conditions (i.e., distance from the coastal edge of the forest or the timing of budbreak) as well as genetic factors.


2020 ◽  
Vol 53 (1) ◽  
pp. 102-108 ◽  
Author(s):  
Eui-Joo Kim ◽  
Young-Ho Jeong ◽  
Jae-Hoon Park ◽  
Eung-Pill Lee ◽  
Seung-Yeon Lee ◽  
...  

2010 ◽  
Vol 5 (10) ◽  
pp. 1934578X1000501 ◽  
Author(s):  
Ling-Li Wang ◽  
Mei-Xiang Jiang ◽  
Sui-Xu Xu ◽  
Qi-Shi Sun ◽  
Guang-Yao Zeng ◽  
...  

Two new acylated flavonoid glycosides have been isolated from the leaves of Quercus dentata Thunb. On the basis of chemical and spectral data, the structures of the compounds have been elucidated as kaempferol 3- O-(2″, 4″-diacetyl-3″- cis-p-coumaroyl-6″- trans-p-coumaroyl)-β-D-glucopyranoside (1), and kaempferol 3- O-(2″- trans-p-coumaroyl-3″, 4″-diacetyl-6″- cis-p-coumaroyl)-β-D-glucopyranoside (2).


2005 ◽  
Vol 118 (3) ◽  
pp. 193-197 ◽  
Author(s):  
Takahide A. Ishida ◽  
Kouhei Hattori ◽  
Satoshi Shibata ◽  
Mayuko Suzuki ◽  
Masahito T. Kimura

2015 ◽  
Vol 10 (3) ◽  
pp. 1934578X1501000
Author(s):  
Yoshikazu Yazaki

A number of colored specialty woods, such as ebony, rosewood, mahogany and amboyna, and commercially important woods, such as morus, logwood, Brazilwood, Japanese yellowwood, blackwood, kwila, red beech and myrtle beech, exhibit a wide range of colors from black, violet, dark red, reddish brown, to pale yellow. These colors are not only due to colored pigments contained in extractives from those woods but also to insoluble polymers. Wood and bark from many species of both hardwood and softwood trees contain many types of flavonoid compounds. Research on flavonoids has been conducted mainly from two points of view. The first is chemotaxonomy with flavonoid compounds as taxonomic markers, and the second relates to the utilization of woods for pulp and paper and the use of tannins from bark for wood adhesives. Most chemotaxonomic studies have been conducted on flavonoids in the extracts from softwoods such as Podocarpus, Pinus, Pseudotsuga, Larix, Taxus, Libocedrus, Tsuja, Taxodium, Sequoia, Cedrus, Tsuga, Abies and Picea. Hardwood chemotaxonomic studies include those on Prunus and Eucalyptus species. Studies on flavonoids in pulp and paper production were conducted on Eucalyptus woods in Australia and woods from Douglas fir in the USA and larch in Japan. Flavonoids as tannin resources from black wattle tannin and quebracho tannin have been used commercially as wood adhesives. Flavonoids in the bark from radiata pine and southern pine, from western and eastern hemlock, southern red oak and Quercus dentata are also discussed. In addition, the distribution of flavonoids among tree species is described, as is the first isolation of rare procyanidin glycosides in nature.


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