Genetic improvements in the mechanical properties of wood are important in forestry species used for lumber, such as Picea. The within-tree radial and among-family variations for the modulus of elasticity (MOE), modulus of rupture (MOR), and their related traits [i.e., microfibril angle (MFA) of the S2 layer in latewood tracheid and air-dry density (AD)] were evaluated in nine open-pollinated families of Picea glehnii (F. Schmidt) Mast. The radial variation in MOR was mainly affected by AD, whereas MOE was affected by MFA and AD. Higher F-values obtained by analysis of variance and coefficient of variation were observed for all properties at the 6th–15th annual ring, except for AD at the 6th–10th annual ring. This result suggests that the contribution of genetic effect is larger in these highly variable regions. In addition, positive correlation coefficients were obtained between wood properties at the 6th–15th annual ring and mean values of these properties. Therefore, genetic improvements for MOE, MOR, and their related traits in P. glehnii is likely to be more effective in juvenile wood, specifically at the 6th–15th annual ring from the pith.
We designed a streamlined timber growth and quality model that aims at the effect of stand management on the efficiency of wood resource use. Applying the R based module toolbox to experimental plots of Douglas fir (Pseudotsuga menziesii [Mirb.] Franco) we analysed essential model features for reflecting the influence of planting density on board strength. The current version realistically predicted a significant increase of centre board bending strength at tree age 40 with initial stand density. Model performance gained clear advantage from a) parameterisation of height to diameter allometry as dependent on planting density b) consideration of cambial age and cross‑sectional knot area in board strength computation. Crown shape was less decisive. The model produced a significant effect of planting density even after a whole rotation period of 70 years as well as a realistic spectrum of board bending strength.
The objective of this study was to investigate basic density and its within-stem variation by studying 84 European aspen stems from 28 forest stands in Latvia. The studied forest stands covered all age classes from young stands to matured forests in representative growth conditions of European aspen. The densities of 2722 wood and 1022 bark specimens were measured from the sampled trees. Only the knot-free wood specimens without obvious wood defects were chosen for analyses. A map of basic density summarizing its radial and axial variations was constructed to show species-specific, within-stem variability and the relationships between density and tree and stand variables were examined. Stem wood and bark of the European aspen show different patterns of basic density variation along the tree stem. Wood density increases from pith to bark up to certain dimensions and shows a slight decrease afterwards. The weighted basic density of bark (446 ± 39.6 kg m–3) was higher than stem wood density (393 ± 30.4 kg m–3). Our results suggest that wood and bark density measurements obtained at breast height can be used for reliable estimation of the densities of whole-tree stem components, while tree parameters such as diameter at breast height (DBH), tree height and social status or stand parameters, including number of trees, basal area and age, are weak predictors in this context.
Estimates of individual heritability and genetic correlation are presented for a set of 10 growth and quality traits based on data from 16 Scots pine (Pinus sylvestris L.) progeny trials in Finland. Seven of the traits (tree height, stem diameter, crown width, Pilodyn value, branch diameter, branch angle and branch number) were objectively measured, whereas three traits (stem straightness, branching score and overall score) were assessed visually. The genetic correlations were mostly moderate or low, and favourable from the tree breeder's point of view. All variables related to tree size correlated relatively strongly and positively. Tree height exhibited a more favourable genetic relationship with the crown form traits than diameter, the latter showing positive correlation with branch diameter. Except for the slight negative correlation between branch angle and branch diameter, the branching traits were not notably correlated. The pilodyn value was positively correlated with stem diameter, reflecting negative correlation between diameter growth and wood density. The highest genetic correlations occurred among the two visually evaluated quality scores and branch diameter. All of the heritabilities were less than 0.4. Overall score, Pilodyn, branch angle, branching score and tree height showed the highest heritability.
Ring width at breast height is presented as a function of stem radius at breast height, the ratio between the diameter of a tree and the basal area median diameter, site index, and density of stand. By means of a conversion model ring width at stump height can be estimated as a function of ring width at breast height.
According to previous studies substantially better wood quality can be expected if mean width near the pith at stump height decreases from 3 to 2 mm. According to the present study only on the poorest sites suitable for Scots pine (Pinus sylvestris L.) planting (poor Vaccinium type) the ring width is less than 3 mm at stump height even in the thickest trees. On more fertile sites a substantial increase in the recommended planting density is required, if the mean ring width is aimed to be less than 3 mm. On the best sites it is impossible to reach mean ring width of less than 2 mm, when the density is less than 4,000 stems/ha. Only the thinnest trees on the poorest sites can have a mean ring width less than 2mm.
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