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1. (Article ID: 12333)
Laitinen M-L, Julkunen-Tiitto R, Rousi M
Variation in phenolic compounds within a birch (Betula pendula) population
Journal of Chemical Ecology 26(7) (2000)
1609-1622
In previous studies, the qualitative and quantitative variation found in defense chemistry among birch populations and even among individual clones has been considerable. However, information about variation among adult, naturally regenerated birch trees from natural populations is still lacking. In this study, the phenolic composition of leaves of 30 naturally regenerated 20-year-old birch (Betula pendula) trees was analyzed for two successive years in order to characterize the chemical composition of individual trees, analyze the annual variation, and determine chemical similarities among individual trees within a population. The main phenolic compounds were flavonoid glycosides, myricetin, and quercetin derivatives. Annual variation in concentration among leaves was large. In most trees, concentrations were markedly higher in 1998 than in 1997; for certain compounds, the detected increase was as much as a 50%. However, for some individual trees, there were no differences between years in chemical quantity. Thus, when selection or grouping of trees is based on secondary chemistry, quantitative variation should be considered carefully. With the qualitative UPGMA method of classification, four chemotypes were found. The grouping was similar for both years, and qualitatively the results of an individual tree seem to be independent of sampling year. The stability in chemical profile of individual trees suggests that quality is tightly controlled by genotype, which provides a recognition tool for chemotaxonomy. The high within-population variation found in leaf defense chemistry may provide protection against different types of insects (generalists or specialists) and, thus, have positive effects on population survival.
variation, population, chemotype, phenolic compounds, birch, Betulaceae, Betula pendula
Publication DOI: 10.1023/A:1005582611863Journal NLM ID: 7505563Publisher: Springer
Correspondence: mllaitin

cc.joensuu.fi
Institutions: Finnish Forest Research Institute, Punkaharju Research Station, Punkaharju, Finland, Department of Biology, University of Joensuu, Joensuu, Finland
The publication contains the following compound(s):
- Compound ID: 19181
Structure type: monomer
Trivial name: miquelianin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
43105, CBank-STR:1426
- Compound ID: 21438
Structure type: monomer
Trivial name: isoquercitrin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
49965, CBank-STR:953
- Compound ID: 21989
Structure type: monomer
Trivial name: hyperoside, hyperin, hyperoside, hyperin, baohuoside-II, quercetin 3-galactoside, vulgarsaponin B
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside, flavanone glycoside
Reference(s) to other database(s): CCSD:
49969, CBank-STR:1983
- Compound ID: 22453
Structure type: monomer
C21H20O11
Trivial name: quercitrin, baohuoside-II, quercetin 3-rhamnoside, quercetin 3-O-rhamnoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49971, CBank-STR:599
- Compound ID: 22462
Structure type: monomer
Trivial name: avicularin, foeniculin, guaijaverin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49972, CBank-STR:524
- Compound ID: 27277
Structure type: monomer
C21H20O12
Trivial name: myricitrin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49968, CBank-STR:384
- Compound ID: 31447
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31837
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31912
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32002
|
b-D-Glcp-(1-3)-Subst
Subst = DHPP = SMILES O{54}C1=CC=C(C(C{3}CO)=O)C=C1 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32003
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
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