Current issue: 57(2)
Under compilation: 57(3)
In this study, logistic regression and neural networks were used to predict non-industrial private forests (NIPF) landowners’ choice of forest taxation basis. The main frame of reference of the study was the Finnish capital taxation reform of 1993. As a consequence of the reform, landowners were required to choose whether to be taxed according to site-productivity or realized-income during the coming transition period of thirteen years.
The most important factor affecting the landowners’ choice of taxation basis was the harvest rate during the transition period, i.e. the chosen timber management strategy. Furthermore, the estimated personal marginal tax rate and the intention to cut timber during next three years affected the choice. The descriptive landowner variables did not have any marked effect on the choice of forest taxation basis.
On average, logistic regression predicted 71% of the choices correctly; the corresponding figure for neural networks was 63%. In both methods, the choice of site-productivity taxation was predicted more accurately than the choice of realized-income taxation. An increase in the number of model variable did not significantly improve the results of neural networks and logistic regression.
A calculation procedure is presented for calculating and analysing remeasured permanent sample plots. Data for eight different fixed and variable size plot types were simulated on the basis of two stands whose trees were mapped and measured in 1982 and 1986. The accuracy and efficiency of the plot types were assessed and compared.
The calculation procedure is based on tree-wise expansion factors and the division of tree sampled into state/measurement classes. Nine classes were required for variable size plots and six for fixed size plots. A relascope plot with basal-area factor 1 (m2/ha) proved to be most efficient for estimating basal-area at a given time and a fixed size circular plot with radius 10 m for estimating basal-area increment over a given time period.
The main problems were related to the estimation of non-measurable variables, e.g., the initial diameters of ingrowth trees, i.e., trees having passed the threshold size during the measurement period. Most problematic were cut trees belonging to the ingrowth or sample enlargement classes. It is nevertheless thought that the system is appropriate for monitoring forest changes and making sensitivity analyses with permanent sample plots.
Semiparametric models, ordinary regression models and mixed models were compared for modelling stem volume in National Forest Inventory data. MSE was lowest for the mixed model. Examination of spatial distribution of residuals showed that spatial correlation of residuals is lower for semiparametric and mixed models than for parametric models with fixed regressors. Mixed models and semiparametric models can both be used for describing the effect of geographic location on stem form.
Fill planting is a common procedure following reforestation in Finland. In 1990, 13% of the total of seedlings planted was used for fill planting. The objective of this study is (i) to survey the survival of fill-in seedlings and (ii) to estimate the spatial pattern of stands to evaluate the importance of fill-in seedlings in constituting the stocking of Scots pine (Pinus sylvestris L.) stands in Central and Northern Finland.
A survey of 63 artificially regenerated Scots pine stands was conducted in 1990. Stand densities varied from 950 to 3,925 seedlings/ha. The mean densities of originally planted, fill planted and naturally regenerated seedlings were 863, 639 and 791/ha, respectively. The survival of originally planted seedlings was 36% and that of fill-in seedlings 48%. Death rate of fill-in seedlings of Scots pine increased with longer times between original and fill planting. The survival rate of Norway spruce (Picea abies) seedlings was correlated with temperature sum. Height of the fill-in seedlings was less than that of the originally planted ones. Most stands had an even spatial distribution with the exception of sparsely populated stands, which were somewhat clustered. This indicates that dying of seedlings is not randomly spread. Because of poor survival, fill planting seems to be a risky business in most cases.
The biomass production and nutrient uptake of silver birch (Betula pendula Roth), downy birch (Betula pubescens Erhr.), grey alder (Alnus incana (L.) Moench), native willows Salix triandra L. and S. phylicifolia L. and exotic willows S. x dasyclados and S. ’Aquatica’ growing on a clay mineral soil field (Sukeva) and on two cut-away peatland areas (Piipsanneva, Valkeasuo) were investigated.
Biomass production of downy birch was greater than that of silver birch, and the biomass production of the native willows greater than that of the exotic ones. The performance of S. phylicifolia was the best of the studied willow species. Exotic willows were susceptible to frost damage and their winter hardiness was poor. The production of all species was lower on the clay mineral soil field than on the cut-away peatland areas. Fertilization of birches and alder – on the double dose given to the willows – increased biomass production. After 6 growing seasons the leafless biomass production of fertilized silver birch at Piipsanneca was 21 t ha-1 (at Valkeasuo 34 t ha-1) and of grey alder 24 t ha-1, and that of S. triandra after five growing seasons 31 t ha-1, S. phylicifolia 38 t ha-1 and of S. x dasyclados 16 t ha-1.
6-year-old stands of silver birch bound more nutrients per unit biomass than downy birch stands. Grey alder bound more N, Ca and Co but less Mn and Zn per unit biomass than silver and downy birch. On the field more P was bound in grey alder per unit biomass compared to downy birch. The willows had more K per unit biomass than the other tree species, and the exotic willow species more N than the native ones. Less N, K and Mg were bound per unit biomass of S. phylicifolia compared to the other tree species.
The effects of repeated fertilizer treatment on biomass production and nutrient status of willow (Salix ’Aquatica’) plantations established on two cut-away peatland areas in western Finland were studied over a rotation period of three years. Comparisons were made between single fertilizer applications and repeated annual fertilization.
The annually repeated fertilizer application increased the amounts of acid ammonium acetate extractable phosphorus and potassium in the soil as well as the concentrations of foliar nitrogen, phosphorus and potassium compared to single application. Depending on the fertilizer treatment and application rate, annual fertilizer application resulted in over two times higher biomass production when compared to single fertilizer application over a three-year rotation period. The effect of phosphorus fertilizer application lasted longer than that of nitrogen. The optimum fertilization regime for biomass production requires that nitrogen fertilizer should be applied annually, but the effect of phosphorus can last at least over a rotation of three years. Potassium fertilizer treatment did not increase the yield in any of the experiments during the first three years. The leafless, above-ground yield of three-year-old, annually NP-fertilized willow plantations was 9.5 t ha-1 and the total biomass, including stems, leaves, roots and the stump, averaged 17 t ha-1.
A multi-factor experimental approach and proportional odds model were used to study interactions between five environmental factors significant to Norway spruce (Picea abies (L.) H. Karst.) seed germination: prechilling (at +4.5°C), suboptimal temperatures (+12 and +16°C), osmotically induced water stress (0.3 Mpa and 0 Mpa), prolonged white light, and short-period of far-red light. Temperature and osmotic stress interacted with one another in the germination of seeds; the effect off osmotic stress being stronger at +16°C than at +12°C. In natural conditions, this interaction may prevent germination early in the summer when soil dries and temperature increases. Prolonged white light prevented germination at low temperature and low osmotic potential. Inhibitory effect was less at higher temperatures and higher osmotic potential, as well as after prechilling. Short-period far-red light did not prevent germination of unchilled seeds in darkness. Prechilling tended to make seeds sensitive to short pulses of far-red light, an effect which depended on temperature: at +12°C the effect on germination was promotive, but at +16°C, inhibitory and partly reversible by white light. It seems that Norway spruce seeds may have adapted to germinate in canopy shade light rich in far-red. The seeds may also have evolved mechanisms to inhibit germination in prolonged light.