Plant Systematics and Evolution

, Volume 298, Issue 2, pp 511–522 | Cite as

Characterization of two chemotypes of Pinus pinaster by their terpene and acid patterns in needles

  • Carlos Arrabal
  • María Concepción García-Vallejo
  • Estrella Cadahia
  • Manuel Cortijo
  • Brigida Fernández de Simón
Original Article

Abstract

The existence of two chemotypes of Pinus pinaster, on the basis of the chemical composition of the resin acids in their needles, is known. An investigation was performed on 54 samples of needles of Spanish Pinus pinaster to study the differences between these chemotypes on the basis of monoterpene, sesquiterpene, neutral diterpene, fatty acid, and resin acid composition. One-hundred and twelve compounds were identified by GC–FID and GC–MS. Statistical analysis of the results established the existence of two groups or chemotypes, in the ratio of 5:1. In one chemotype, total acid compounds were more abundant than neutral compounds, whereas in the other the concentrations of both neutral and acid compounds were similar. Distinction of the chemotypes was based on the presence/absence of a sesquiterpene (germacrene d-4-ol acetate), neutral diterpenes (8(14),13(15)-abietadiene, anticopalol, an isomer of anticopalol, and pimarol), fatty acids (10-octadecenoic, 14-hydroxy-10-octadecenoic, and 13-hydroxy-9-octadenoic acids and an unidentified fatty acid), and resin acids (levopimaric + palustric, eperuic, and anticopalic acids, and three isomers of anticopalic acid); and on the different relative percentages of other compounds of these types. This study gives a wide view of the composition of the needles of Pinus pinaster, improving the differentiation of chemotypes on the basis of terpene and acid composition.

Keywords

Pinus pinaster Needles Chemotypes Terpenes Acids 

Notes

Acknowledgments

This work was financially supported by Project SC97-118-C2-1 from MAPA (Ministry of Agriculture, Fisheries and Food, Spain). We wish to thank Dr Duane F. Zinkel for kindly supplying authentic samples of some resin acids and Dr Ricardo Alía for his valuable assistance.

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Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Carlos Arrabal
    • 1
  • María Concepción García-Vallejo
    • 2
  • Estrella Cadahia
    • 2
  • Manuel Cortijo
    • 1
  • Brigida Fernández de Simón
    • 2
  1. 1.Departamento de Ingeniería ForestalUniversidad Politécnica de Madrid, Escuela Técnica Superior de Ingenieros de MontesMadridSpain
  2. 2.Departamento de Industrias ForestalesINIA-CIFORMadridSpain

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