Morphological and foliar terpene characters to distinguish between western and eastern white pine

1990 ◽  
Vol 68 (11) ◽  
pp. 2525-2530 ◽  
Author(s):  
R. S. Hunt ◽  
M. D. Meagher ◽  
J. F. Manville

To distinguish between western (Pinus monticola) and eastern (P. strobus) white pines, foliage, buds, and cones were examined and foliar terpenes were extracted and analyzed from representative samples. Needles of P. monticola were heavier, wider (>0.7 mm), and stiffer; buds were larger and usually nonresinous; cone scales, when viewed from the cone bottom, were arranged in five and eight spiralling rows. Needles of P. strobus were lighter, narrower (<0.7 mm), and droopy; buds were small and covered with white resin and bloom; cone scales were arranged in three and five rows. Needles and cones of P. monticola tended to be longer; cones were composed of more scales and contained more scales per centimetre and more scales per spiral row than those of P. strobus, but there was some overlap. Twig pubescence, bud apex shape, phyllotaxy, and seed wing length were not distinctive. Capillary gas-liquid chromatographic analysis of the leaf oils of white pine trees showed that bornyl acetate and β-elemene, present in P. monticola, were essentially absent in P. strobus, while α-humulene, present in P. strobus, was not found in P. monticola. In addition, the amount of β-caryophyllene could be used to differentiate between these species. However, the most obvious discriminating feature was the presence of a substantial and broad peak of unknown and decomposing compound(s) in the chromatograms for P. monticola and its complete absence in the chromatograms for P. strobus. A clone that was highly resistant to blister rust and previously classified as P. monticola is shown by terpene patterns and morphology to be P. strobus. Key words: Pinus monticola, Pinus strobus, terpene, Cronartium, morphology.

1973 ◽  
Vol 3 (4) ◽  
pp. 516-521 ◽  
Author(s):  
G. D. Sinclair ◽  
D. K. Dymond

The distribution of acetone-soluble extractives in jack pine trees of different diameters, and at different locations within a single tree was studied. The amount of extractives varied from 3% in a 10 cm diameter tree to 9.6% in a 50 cm diameter tree. Within a single tree the top had the least amount of extract, 2.7%, while the needle bearing twigs had the greatest amount, 4.6%. Gas–liquid chromatographic analysis of the extracts showed that the composition was relatively similar for all sizes of trees and within one tree except in the top and the branches. The heartwood of the tree had a much higher extractive content than the sapwood and contained a higher concentration of resin acids, pinocembrin, and pinobanksin.


1998 ◽  
Vol 28 (3) ◽  
pp. 412-417 ◽  
Author(s):  
Abul KM Ekramoddoullah ◽  
Joanne J Davidson ◽  
Doug W Taylor

A 19-kDa protein, Pin m III, was recently shown to be associated with overwintering and frost hardiness of western white pine (Pinus monticola Dougl. ex D. Don) seedlings. Here, we report that this protein is up-regulated by the fungus Cronartium ribicola Fisch, the causal agent of white pine blister rust in western white pine trees. Between 1991 and 1994, bark samples of mature western white pine trees (resistant with no stem cankers and susceptible with stem cankers) were collected in winter, spring, and fall. Proteins were extracted and analyzed by Western immunoblot utilizing specific rabbit polyclonal anti-Pin l I (a homologue of Pin m III) antibodies. During all collection dates, but particularly in the spring, susceptible trees had more Pin m III than resistant trees. In July 1995, 43 previously inoculated 7-year-old white pine seedlings were also analyzed. In all susceptible seedlings (cankered) tested, cankered tissue had high levels of Pin m III, and samples collected from the outside edge of the canker margin had low levels of Pin m III; this protein was also detected in some healthy bark of cankered trees. Since the level of Pin m III in healthy white pine trees is normally lowest in summer months, the high level Pin m III in summer samples of infected tissues is a consequence of the fungal infection.


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