Current issue: 58(5)
A process-oriented tree and stand growth model is extended to be applicable to the analysis of timber quality, and how it is influenced by silvicultural treatments. The tree-level model is based on the carbon balance and it incorporates the dynamics of five biomass variables as well as tree height, crown base, and breast height diameter. Allocation of carbon is based on the conservation of structural relationships, in particular, the pipe model. The pipe-model relationships are extended to the whorl level, but in order to avoid a 3-dimensional model of entire crown structure, the branch module is largely stochastic and aggregated. In model construction, a top-down hierarchy is used where at each step down, the upper level sets constraints for the lower level. Some advantages of this approach are model consistency and efficiency of calculations, but probably at the cost of reduced flexibility. The detailed structure related with the branching module is preliminary and will be improved when more data becomes available. Model parameters are identified for Scots pine (Pinus sylvestris L.) in Southern Finland, and example simulations are carried out to compare the development of quality characteristics in different stocking densities.
The study based on young Scots pine (Pinus sylvestris L.) of varying density showed that number of living branches per whorl and total number of living branches per tree were negatively correlated with stand density. On the contrary, the number of dead branches increased with increasing stand density. The diameter of living and dead branches decreased with increasing stand density. Consequently, the branchiness, i.e. the share of the branch cross-sectional area from the surface area of the stem, decreased in dense stands compared with the thin stands. At the densest stands the branchiness, however, levelled of indicating a greater decrease of the radial growth at stems than at branches. The 2/3 power law described relatively well the relationship between stand density and mean squared branch diameter of living branches.
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A study based on four young Scots pines (Pinus sylvestris L.) showed that the number of needle-covered shoots per crown volume unit was independent on tree position representing a constant value of 600–700 shoots/m3. This was true, even though the total shoot number decreased with deteriorating tree position. In tree crown there were fourth-order shoots in good light conditions but only first- and second-order-shoots, when light conditions were poor. The length of shoots decreased in accordance with increasing order of the shoot.
The share of the needle biomass and growth increased, when the shoot order increased. Similarly, the share of needles increased with deteriorating tree position. This was especially true in the upper crown. On the other hand, the share of the crown from the total biomass and growth increased with improving tree position. The percentage of crown system of a dominant tree in a sparse stand was 64% of that of biomass and 83% of that of growth. The corresponding values for a suppressed tree in a dense stand were 36% and 35%. The growth of wood, bark and needles in crown systems was linearly correlated with prevailing light conditions around the branch. It is evident that the tree position and light condition within the stand control the wood, bark and needle growth in the crown system and their interrelationships.
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Empirical measurements showed that the strength of a dead branch of Scots pine (Pinus sylvestris L.) was related to the second power of the branch diameter and the third power of the basic density of branch wood. The same factors affected also the strength of living branches. Especially, the contribution of wood density was important. The significance of the results is discussed considering the natural process of self-pruning and its effect on the branchiness of the stem.
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In the study the proportion of branch samples of various diameter were studied. The branches were taken from small trees to be harvested by total tree chipping method. The material consisted of 1,056 branch samples of birch (Betula verrucosa, now B. pendula Roth, and Betula pubescens Erhr.), Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) at intervals of 20 cm along each branch.
With exception of the basic density of bark, there was a relation between all the other properties which were studied and the diameter. Even when the effect of diameter was eliminated, in many cases the effect of the distance of the samples from the stem became apparent.
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Pruning growing trees influences tree growth and value of the wood and yield of timber of the stand. Pruning living branches create open wounds on the stems that can risk the growth of tree species that are vulnerable to injuries. For instance, pruning has been shown to cause decay in Norway spruce (Picea abies (L.) H. Karst.), while Scots pine (Pinus sylvestris L.) can quickly heal over the branch scars. Pruning of living branches reduces the crown, the effect of which remains small if only the lowest branches are pruned. Pruning of dry branches has little effect on the health of the tree. The main objective of pruning is to improve the quality of timber. Knottiness decreases strength and appearance of timber. Pruning increases the yield of knot-free sapwood, which is especially valuable in veneer timber. Pruning is, therefore, at present most suitable for birch and aspen which are used in veneer industry. In both species pruning should be directed mainly to dry branches.
The PDF includes a summary in German.