Non-structural carbohydrates in silver birch (Betula pendula Roth) wood were analysed in a 7-yearold clone and in five mature stems. The analysis was conducted to obtain more detailed information on seasonal fluctuation of these components and of the tree-totree variation and within stem variation. The sugars were analysed by GLC-MS. The smallest total soluble sugar amounts (consisting of sucrose, fructose, glucose, raffinose and myo-inositol) in young trees were measured during mid-summer (ca. 0.3%) and the largest while in dormancy (ca. 1.6% on wood dry weight basis). Raffinose was detected in autumn as a minor component. The proportion of monosaccharides and the amount of myoinositol were largest during growth. Compared to other studies silver birch showed more evident seasonal fluctuation in soluble sugars than evergreen tree species. The sugar amount in mature stems was approximately at the same level as in young trees that had the same felling time. Tree-to-tree variation in the non-structural carbohydrates in the mature wood was fairly large. However, the amount of total soluble sugars, sucrose and glucose showed significant variation within the stem. The amount of these sugars was largest in samples that were taken close to the cambium. Starch was also detected close to pith. According to the heartwood definition and starch measurement results in this paper, it could be stated that silver birch does not form heartwood.
Three-year old Betula pendula Roth clones were grown at two nutrient levels in a field experiment to investigate the responses and recovery in growth and wood properties to a range of defoliation levels (0100%). No general threshold value of defoliation level for negative effects in growth was found, since the sensitivity of saplings to defoliation varied according to plant traits studied. However, responses were related to defoliation intensity. Saplings compensated for 25% defoliation in terms of height growth and number of current branches and were able to tolerate 50% defoliation without effects on diameter growth 1 year after the defoliation. Nutrient availability was significant only in determining how total biomass responded to defoliation. Fertilized saplings were able to tolerate 25% defoliation without reduction in total biomass, but nonfertilized saplings were not. The interaction between defoliation and fertilization disappeared in the second growing season after the defoliation. Saplings were not able to compensate for 75% defoliation in terms of total biomass or for 100% defoliation in terms of growth and branching even in 2 years' recovery time. In stemwood, complete defoliation reduced growth ring width and vessel diameter simultaneously and also induced a narrow zone of secondary xylem with defects. Our results suggest that defoliation level and recovery time played a crucial role in compensatory growth of birch saplings, while nutrient availability had a minor role.
Variations in the concentration and composition of triacylglycerols, free fatty acids and phospholipids were analyzed in Scots pine (Pinus sylvestris L.) trees at five sites. Disks were taken at breast height or at a height of 4 m from the stems of 81 trees differing in diameter and growth rate. The mean concentration of triacylglycerols in sapwood was 26 mg g(-1) dry mass; however, variation among trees was large (16-51 mg g(dm)(-1)). The concentration of triacylglycerols was slightly larger at 4 m height in the stem than at breast height. Concentrations of triacylglycerols did not differ between the sapwood of young and small-diameter stems (DBH < 12 cm) and the sapwood of old stems (DBH > 36 cm). Concentrations of free fatty acids were negligible in the outer sapwood, but ranged between 5 and 18 mg g(dm)(-1) in the heartwood. The most abundant fatty acids of triacylglycerols were oleic (18:1), linoleic (18:2omega6, 18:2Delta5,9), linolenic (pinolenic, 18:3Delta5,9,12 and 18:3omega3) and eicosatrienoic acid (20:3Delta5,11,14 and 20:3omega6). The concentration of linoleic acid comprised 39-46% of the triacylglycerol fatty acids and the concentration was higher in the slow-growing stem from northern Finland than in the stems from southern Finland. Major phospholipids were detected only in sapwood, and only traces of lipid phosphorus were detected in heartwood.
This study focused on wood density and annual ring width in Norway spruce (Picea abies (L.) Karst.) grown in uneven-aged stands (UAS). In total, 96 trees were harvested from five UAS that had been managed by single-tree selection for decades. A data set of 27 trees from even-aged stands (EAS) was used for comparison. In the UAS trees, high density and narrow annual rings were found in the juvenile wood near the pith. Thereafter, wood density rapidly decreased until the 20th annual ring, followed by an increase toward the bark. In the outermost rings, wood density again slightly decreased. The trends in wood density in the UAS trees correspond with those reported for naturally regenerated, even-aged Norway spruce stands, with the exception of the decrease in the outermost rings. A mixed linear model with ring width, cambial age, and canopy position as fixed parameters accounted for 53% of the variation in wood density of the UAS trees. In contrast to UAS trees, EAS trees showed increased wood density in the outer rings as a result of decreasing growth rate. The abrupt change in wood density of UAS trees may affect the properties of timber sawn close to the pith.
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