Models for individual-tree basal area growth were constructed for Scots pine (Pinus sylvestris L.), pubescent birch (Betula pubescens Ehrh.) and Norway spruce (Picea abies (L.) Karst.) growing in drained peatland stands. The data consisted of two separate sets of permanent sample plots forming a large sample of drained peatland stands in Finland. The dependent variable in all models was the 5-year basal area growth of a tree. The independent tree-level variables were tree dbh, tree basal area, and the sum of the basal area of trees larger than the target tree. Independent stand-level variables were stand basal area, the diameter of the tree of median basal area, and temperature sum. Categorical variables describing the site quality, as well as the condition and age of drainage, were used. Differences in tree growth were used as criteria in reclassifying the a priori site types into new yield classes by tree species. All models were constructed as mixed linear models with a random stand effect. The models were tested against the modelling data and against independent data sets.
The prescribed burning of a 7.3 ha clear-cut and a 1.7 ha partially cut forest (volume 150 m3/ha) was carried out in Evo (61 °12'N, 25°07'E) on 1 June 1992. The forest was a mesic Myrtillus site type forest dominated by Norway spruce (Picea abies (L.) H. Karst.). Practically all the trees and the above-ground parts of the understorey vegetation died in the fire, while the mor layer was thinned by an average of 1.5 cm.
A study was made on the change of germinated seedling population in time and their dependence on environmental factors. Seedlings of Norway spruce, Scots pine (Pinus sylvestris L.), silver birch (Betula pendula Roth), pubescent birch (B. pubescens Ehrh.) and rowan (Sorbus aucuparia L.) were inventoried in 1993 and in 1994 on permanent plots, four times per growing season. Autoregression models were used to compare regeneration of tree species in the burned forest with regeneration in the burnt clear-cut area, and to study the effect of distance from nearest seed source to regeneration.
The average number of seedlings germinating in 1993 was higher than in 1994, probably because of differences between these consecutive years in regard to the amount of seed rain and weather conditions. The number of Norway spruce and rowan seedling was higher inside the forest area than in the clear-cut area. The distance to the bordering forest and to the closest seed tree did not explain the result. It is suggested that the more stable microclimatic conditions under the shade of dead tree promote germination and seedling establishment in the forest area. As rowan is a bird-dispersed species, it is likely that dead trees help the dispersal of rowan seed by providing birds place to sit and defecate. The shade provided by dead trees may influence the further succession of the tree stand and vegetation composition and diversity.
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.
Refertilization with PK, about 15 years after the first fertilizer application, increased tree growth and the amount of nutrients in tree litter in Scots pine (Pinus sylvestris L.) and birch (mainly Betula pubescens Erhr.) stands on a drained fertile mire in Northern Finland (65°34 N’, 25°42’ E). The increase in growth and nutrient contents after refertilization was greatest in the mature pine stand where the application of nitrogen and micronutrients gave an additional response compared to the PK-application.
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In the model the regeneration process is derived into three subprocesses: birth, growth and mortality of seedlings. The main emphasis is on the birth process where the following phases are simulated: seed crop, quality of seeds, maturity of seeds, predation of seeds and germination. The parameters are based on data published in Finland. Part of the parameters are obtained directly from the investigations and part is proposed by the author. The model can be calibrated by changing parameter values. The simulation is made with the help of random numbers which have the same means as the estimates and the same distributions as the residuals of the equations used in simulation. The time step of the model is one year. The number of emerged seedlings in one year is obtained by multiplying the seed crop with the probabilities that the seed passes different phases of the birth process. Because of stochasticity the regeneration period is simulated several times. From the results it is possible to evaluate the risk and succeeding probability of the regeneration. The main drawbacks of the simulation method are the lack of empirical parameters and the difficulty of testing. The model could be further developed by including spatiality into the model.
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A model was developed in order to describe the peeling of veneer for determining value relationship for birch veneer logs and stems. The model was based on selling prices of veneer and other products as well as processing costs. The model was utilized for determining the effect of various input variables on the log value.
According to the results, the effect of tree size was important for the value of raw material. Even knottiness had an effect although only in the higher manufacturing costs of knotty veneer were taken into account. Pruning was a method to increase substantially the proportion of knotless veneer.
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The susceptibility of Betula pendula Roth and B. pubescens Ehrh. Saplings to stem spot disease caused by Godronia multispora J.W. Groves and Fusarium avenaceum (Fr.) Sacc. was studeied. B. pendula proved to be more susceptible than B. pubescens on all studied soils, especially on peat. G. multispora was more pathogenic than F. avenaceum. Inoculations with G. multispora in the spring and summer induced smaller cancers than in the autumn.
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There are great impact forces in mechanized harvesting and wood yard in the mills which can cause breaks in timber. The impact strength of timber in green condition was tested in temperatures of +18°C and -18°C using sawn pieces (20 x 20 x 300 mm) of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.), birch (Betula pendula Roth and B. pubescens Ehrh.), grey alder (Alnus incana L.) and aspen (Populus tremula L.). In addition, unbarked naturally round sticks (length 300 mm, diameter 15 and 35 mm) of the same species were tested.
The impact strength of round sticks was 1.5–4.4 times as great as that of sawn pieces. The reasons are possibly the avoidance of cell breaks at the surface as well as growth stresses. The frozen samples were clearly weaker than the unfrozen ones. As a rule, the impact bending strength increased with increased density of the species. However, the correlation varied greatly between species. If density was kept constant, an increase in the growth ring width decreased the impact strength. The reason may lie in the fracture mechanism.
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Young Norway spruce (Picea abies (L.) H. Karst.) are susceptible to early summer frost damage. Birch (Betula pubescens Ehrh.) naturally colonize rich or fairly rich drained peatlands after clear cutting, and can provide protection for developing seedlings. The report describes the development of spruce stands after various types of handing of the birch nurse crops.
Different proportions of birch and spruces did not have any influence on the spruce stand production. In cases where the nurse crop stand is removed when the spruce stand age was 20 years and height 4 m the spruce suffered badly but recovered with time, reaching the spruce stand growing under a nurse stand within the next 20 years. The height growth of spruce depends on the density of the nurse stand, especially on fertile sites. The development of diameter growth also depends on the density of the nurse trees. Removal of the nurse stand in spruce stands on the sites concerned should be done when the spruce stand is 20 years old and at the height of 4 m.
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The anatomical variation of a lateral root was compared with that of the stem of the same tree at breast height by concentrating on the intrelationships of certain anatomical features in Betula pendula and B. pubescens. The results showed that root wood has several essential features of stem wood, such as gelatinous fibres, growth eccentricity, scalariform perforation plates in the vessels and pith flecks. However, some of the anatomical differences are significant. The differences between the species were more pronounced in the root than in the stem anatomy.
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Ten trees of mountain birch (Betula tortuosa Ledeb, now Betula pubescens subsp. czerepanovii) with an average age of 39 years were sampled in northern Lapland in Finland. The average green density of wood was 589 kg/m3 and that of bark 941 kg/m3. The basic densities were 520 kg/m3 and 559 kg/m3, respectively. The basic density increased only little from the pith to the surface. In contrast, the number of bars in the perforation plates of the vessels increased considerably in the same direction. The average number of bars was 17.3.
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Downy birch (Betula pubescens Ehrh.) trees growing on a drained peatland were cut during dormancy. The properties of the one-year old shoots produced by the stumps were measured in the autumn after one growing season. The one-year old willow shoots (a mixture of Salix phylicifolia L., S. pentandra L. and S. caprea L.) were collected from an abandoned field.
The basic density of unbarked shoots was 443 kg/m3 for birch and 346 kg/m3 for willow. The basic density of the bark was much higher than that of the wood. The effect of shoot length on the properties was small with the exception of cellular proportions. The fibre percentage increased and vessel percentage decreased with increasing shoot length.
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Length variation of fibres and vessels was studied in the branches, stems and roots of Betula pendula Roth and B. pubescense Ehrh. The cells were significantly shorter in the branches and roots than in the stems. There was no significant difference in the cell length between the upper and lower radii of the branches and roots. The length increased from the pith to the surface and decreased in the branches and stems from the base onwards. In the roots the length increased in that direction. The differences between the tree species were small although the cells of B. pubescens were a little longer.
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Variation of wood characteristics was studied in two mature trees of Betula pendula Roth and two of B. pubescens Ehrh. by stressing the interrelationships of some of the structural features, basic density and shrinkage. Correlation analysis revealed that basic density was related to some of the variables studied, viz: number of rings (age) and distance from pith, height from the ground, ring width, fibre length and double wall thickness. Multiple regression equation showed that age from pith and height from the ground explained 80% of variation of basic density in B. pendula. Two structural variables, viz: fibre wall thickness and ring width accounted for only 28% of variation of basic density in B. pubescens. No significant relations could be found between shrinkage and any of the wood parameters measured in B. pendula while some of the relationships were significant in B. pubescens. However, only 55% of variation of volumetric shrinkage was explained by two related factors, viz: basic density and moisture content while only 35% of variation of tangential shrinkage was explained by ring width and fibre width. Increase in fibre length was highly associated with the increase in fibre width, double wall thickness and vessel length in either species.
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It was concluded on the basis of the anatomical investigations of four mature trees that Betula pendula Roth can be distinguished from B. pubescens Ehrh. using the number of bars per scalariform perforation plate as an identification factor. If the average number of bars is more than 17.6, the sample is probably from B. pubescens, and if less, from B. pendula. The accuracy can be slightly improved by using the vessel frequency as another factor.
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Samples that had extensive pith flecks, caused by the larvae of Dendromyza betulae (now Phytobia betulae E.Kang), were collected from two trees of Betula pendula Roth and two B. pubescens Erhr. The age of the trees varied from 45 to 56 years. The effect of larvae injury on the rays was studied. The width of affected rays in both species was more than twice that of normal rays. The height and frequency also increased considerably. When describing the anatomy of Betula species the pith flecks should be treated with caution in order to avoid confusion and misinterpretation.
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The aim of this study was to determine under what conditions and with what premises the growing of Betula pubescens Ehrh. is an economically competitive alternative to the growing of Scots pine (Pinus sylvestris L.) in drained peatlands. The basic material consisted of all drainage projects in Ostrobothnia in Western Finland in 1937–38 and 1957–59, according to the archives of the Central Board of Forestry Tapio, including such areas that were at least moderately fertile and had birch dominated young stands or no tree cover. A total of 202 sample plots were measured.
According to the results, the discounted timber yield of the thinned B. pubescens stands is about 10% greater than that of untreated stands. The removing of birch seedlings and the subsequent growing of fully stocked Scots pine is more profitable than growing B. pubescens stands only if the establishment and subsequent development of the pine stand involve no costs. If the site in question is a fertile open drained peatland, establishment of a pine stand is obviously a better financial proposition than a naturally regenerated birch stand. However, if there is already a fully stocked young birch stand on the site, it is more economical to let it grow using a shortish rotation time.
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The study was carried out in order to find out the changes taking place in germination of seeds in certain tree species as a function of gamma irradiation, the height growth of the seedlings produced and the types of phenotypic mutants possibly found in the generation that had received radiation. The tree species studied were Pinus sylvestris L., Picea abies (L.) H. Karst., Betula verrucosa (Betula pendula Roth), B. Pubescens Ehrh., Alnus glutinosa (L.) Gaertn. and Alnus incana (L.) Moench.
Soaked seeds that had received a rather small dose of radiation germinated usually better than storage-dry seeds, B. pubescens being an exception. The damages observed in germination, height growth and the relative number of mutants were greater the higher the irradiation doses. The LD50 dose (germination, 28 days) was as follows in the case of the different tree species (storage dry/soaked): P. Sylvestris 1,500-2,000/2500-3,000, P. abies 1,000-1,500/4,000-4,500, B. pendula 9,500-10,000/7,000-7,500, B. pubescens >10,000/7,500-8,000 and A. Glutinosa 10,000/8,500-9,000 rad. Mass production of different mutants of deciduous trees for ornamental purposes, for example, appears to be easy using gamma-irradiation. On the other hand, the possibility of increasing tree growth remains open for further study.
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The ash content has been found to correlate with the fertility of peatlands. Relationship between height of 80-year-old stands and ash content of peat in topmost 30 cm layer was examined in Lithuanian conditions. On drained peatlands with ash content of peat from 3% to 8% pine stands increase in height. Ash content of peat being about 7% Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) stands on drained sites are found to be of equal height. Ash content of peat more than 8–9% has no significant effect on growth of pine or spruce stands. Birch (Betula verrucosa (B. Pendula Roth.) and Betula pubescens Erhrh.), stands are less sensitive to ash content of peat compared with other species. Black alder (Alnus glutinosa L. Gaertn.) stands occurred in sites with ash content of peat more than 8–10%. The height of the stands become equal both in drained and undrained sites in the cases where ash content of peat is about 16–18%. Ash (Fraxinus exelsior L.) stands attain high productivity on drained sites with ash content of peat about 20%.
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The objective of this investigation was to study the influence of stand density of white birch (Betula pubescens Ehrl.) on the minimum temperatures in the stand during the growing season, and the actual minimum temperatures of the leading shoot of Norway spruce (Picea abies (L.) H. Karst.) seedlings growing in the open. The 40-year-old uniform white birch stand was situated in 142 m above the sea level in Southern Finland. The stand was treated with thinnings of three different densities in 1961.
Air temperature was recorded in four sample plots at heights of 0.1 m, 0.5 m, 1.0 m, 2 m and 4 m. In the stand of moderate density, temperatures were measured at heights of 6.0 m, and in the stand of full density at 6.0 m, 8.0 m and 10.0 m.
The temperature differences between stands of various densities proved to be rather small. Especially the thinnest stand differed very little from the open area. The soil surface has in all cases been warm compared with the higher air layers indicating meadow-fog-type by Geier (1965). On cloudy or windy weather all the temperature profiles in the various stands resembled each other. The difference between the air temperature and temperature of the spruce shoot was greatest at midnight and decreased steadily thereafter.
The problem in using shelter stands for spruce regeneration areas is that optimum shelter stand density is difficult to define. Already a thin shelter stand causes drawbacks to the young seedlings, but in order to be effective enough against early frosts, the shelter stand should be comparatively dense.
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The study is continuation of the earlier structure and growth studies of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) in Forest Research Institute. The material represents birch stands (Betula verrucosa, now B. pendula, and B. Pubescens L.) in Southern Finland. The stands were treated with different fellings, and in regard to their silvicultural condition classified as good, satisfactory and unsatisfactory. Height of the trees, height of living crown, volume, increment and volume increment and development of stem diameter series was measured.
The most characteristic difference between the silviculturally good and poor stands was that the the annual increment of the good stands concentrated into large size trees, and the increment of unsatisfactory stands into small and inferior trees.
It is concluded that if the aim of stand treatment is to produce large and high quality volume increment, the most favourable stand volume of birch stands, compared with naturally normal stand volume, seems to be 90-85% at the age of 41-55 years, and 80-70% at the age of 56-65 years. If growth of large size trees is aimed at, the maximum number of the dominant trees per hectares cannot be more than 400 at the age of 50-60 years.
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The article is based on the writer’s visits in the area in 1933 and 1939. Pyhätunturi national park was established in 1938. The fell of Pyhätunturi rises up to 540 meters above the sea level, and 357 meters above the surrounding area. The soil is predominantly stony, and the rock is quartzite. The climate is continental with low rainfall. This results in a barren area, where array of plant species is limited with the exception of few gorges with fertile river valleys. The forests have remained mostly in natural state.
Vegetation is arranged in three zones: forested area, subalpine fell birch area and alpine bare top of the fell. Scots pine (Pinus sylvestris L.) forms timberline more often than Norway spruce (Picea abies (L.) H. Karst.). Coniferous forests rise up to 365 meters on the northern slopes and up to about 385 on the southern slopes of the fell. It is followed by fell birch zone (Betula tortuosa, now Betula pubescens subsp. Czerepanovii) up to about 450-475 meters on the eastern and northern slopes, and 475-490 meters on the western slopes. The most common forest site type is Empetrum-Myrtillus site type. Herb-rich spruce swamps along the rivers have highest diversity of species. The article describes the plant species found in forests, peatlands, fell birch zone and top of the fell in detail. In all 162 different vascular plant species and 16 non-indigenous species were found in the area.
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The objective of the present investigation was to clarify the profitability of pruning silver birch (Betula verrucosa, now Betula pendula Roth) in the growing of raw material for veneer industry. Calculations were made on the grade, value, and price of pruned and untreated butt logs as well as on costs of pruning and the development of pruned trees.
The grade distribution of unpruned veneer butt logs, the grade distribution of the veneer yield, and consequently, the value of veneer yield and log prices at the plant are considerably better than those of average logs. The grade, value and price increased with increasing diameter. The value and price of pruned butt logs depended primarily on the difference between the turning pruning diameters, and their increase with decreasing pruning diameter and increasing turning diameter. The value of pruned butt logs is always considerably higher than that of unpruned logs. The increase in the value correlates to the pruning and turning diameters, and is, for example, in rotary-cut logs which have been pruned when 10 cm in diameter 80–130%.
Pruning increases the stumpage in naturally regenerated silver birch stands on Oxalis-Myrtillus site by 2,000–3,000 Fmk/ha when employed at 20 years of stand age and rotary cutting at 60–80 years of age respectively. The average pruning costs on Oxalis-Myrtillus site are 51–57 Fmk/ha.
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The objective of the investigation was to determine the differences between faultless timber grown on a peatland before and after draining, in respect of compressive strength to the grain, volume weight, and shrinkage. In addition, the influence of the boundary zone between the close-ringed wood formed before draining and the wide-ringed wood produced after draining on strength of the timber was studied. The material consisted of 15 sample trees of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) Karst.), white birch (Betula pubescens Ehrh.) and silver birch (B. Pendula Roth).
The volume weight of wood of the tree species in ascending order is; spruce, pine, white birch, silver birch. The volume weight of Scots pine seems to decrease from the butt end upwards, while no trend was revealed for spruce. In the coniferous trees, the wide-ringed wood formed subsequent to draining was slightly lighter than the close-ringed wood produced prior draining. No distinct trend was seen in the birch species. The volume weight of pine and spruce increased with decreasing width of the growth rings up to a certain limit, after which the conditions inverted.
The compressive strength of the different kinds of wood seems to increase from the butt end upwards, but after height of two meters it begins to decrease considerably. In birch, this point of inversion is in somewhat greater height. In spruce timber, the compressive strength parallel to the grain is lowest for wood which contains exclusively wide-ringed wood formed after draining. The boundary zone between the woods formed before and after draining is very distinguishable, but has no remarkable influence on the compressive strength parallel to the grain. Shrinkage of close-ringed wood is higher in all three principal directions than that of wide-ringed wood. This can be explained by the variations in volume weight and fibrillar orientation of the tracheid walls.
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The investigation concerns with the strength of the eccentric growth accompanying formation of tension wood in silver birch (Betula pendula Roth.) and downy birch (Betula pubescens Ehrh.), behaviour of wood in wood-working machines and its macroscopic characteristics, its microscopic and sub-microscopic structure, chemical composition, resistance against certain chemicals, physical properties, and the strength characteristics of wood.
The most detrimental properties of tension wood used in wood working industry are high longitudinal shrinkage, warping, twisting and checking. The wooliness of the cut is unwanted, for instance, in plywood and furniture. In pulp industry tension wood is better raw material than normal wood because it yields more and purer cellulose than normal wood. However, it has poorer strength properties.
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Birch wood is used widely in wooden structures where mechanical strength is needed. The aim of the research was to study the influence of the relative share of mechanically weak tracheids, and length of the wood fibers on specific gravity and bending strength of downy birch (Betula pubescens Ehrh.) wood. According to the results, the strength of wood is strongly dependent on the relative share of tracheids, and length of the libriform cells. The strength of the wood increases when the share of tracheids decreases and the length of libriform cells increases. The specific gravity can be used as an indication of the strength of wood, especially if it is possible to analyze the structure of the wood.
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The subarctic-subalpine mountain birch forest zone discerns Fennoscandia from other northern regions. The zone offers protection against wind to animal life, protects soil from evaporation and increases humidity. The article reviews distribution of vertebrate and butterfly species in the birch forest zone. There are no vertebrates that occur solely in the birch forest zone, and only few live mostly in the zone. Many species live either both on the birch forest zone and the treeless fell area above it, or in the birch forest zone and coniferous zone below it. Similarly, no butterflies occur only in the birch forest zone, but the zone is the main habitat for some species. Consequently, the subarctic-subalpine birch forest zone cannot be considered to be an independent ecozone but a transitional zone between regio silvatica and regio arctica that is nearer to the northern coniferous zone than the fell region
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In South-West Finland the usual method to make leaf fodder for cattle has been to cut the branches and collect the new sprouts again next year. According to this review, the most common tree species to be topped is Betula sp. Downy Birch (Betula pubescens Ehrh.) grows shoots easier than silver birch (B. pendula Roth). The topped forests are usually small and situated near the settlements, next to the fields and meadows. The birch trees are typically cut when they are 15-20 years old. Regularly topped birch rots easily and seldom exceeds 50 years. The capacity to grow shoots depends on the age of the tree, site and time of the cutting. The risk for rotting can be decreased by removing only part of the shoots and cutting the shoots a short distance from the base of the shoot. Collecting leaf fodder decreased in Finland, and was common only in the South-West Finland and Åland.
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Male flowering was studied at the canopy level in 10 silver birch (Betula pendula Roth) stands from 8 localities and 14 downy birch (B. pubescens Ehrh.) stands from 10 localities in Finland in 1963–73. Distribution of cumulative pollen catches was compared to the normal Gaussian distribution. The basis for timing of flowering was the 50% point of the anthesis-fitted normal distribution. To eliminate effects of background pollen, only the central, normally distributed part of the cumulative distribution was used. Development was measured and tested in calendar days, in degree days (> 5°C) and in period units. The count of the parameters began in March 19.
Male flowering in silver birch occurred from late April to late June depending on latitude, and flowering in downy birch took place from early May to early July. The heat sums needed for male flowering varied in downy birch stands latitudinally but there was practically no latitudinal variation in silver birch flowering. The amount of male flowering in stands of the both species were found to have a large annual variation but without any clear periodicity.
The between years pollen catch variation in stands of either birch species did not show any significant latitudinal correlation in contrast to Norway spruce stands. The period unit heat sum gave the most accurate forecast of the timing of flowering for 60% of the silver birch stands and for 78.6% of the downy birch stands. Silver birch seems to have a local inclination for a more fixed flowering date compared to downy birch, which could mean a considerable photoperiodic influence on flowering time of silver birch. The species had different geographical correlations.
Frequent hybridization of the birch species occurs more often in Northern Finland than in more southerly latitudes. The different timing in the flowering causes increasing scatter in flowering times in the north, especially in the case of downy birch. Thus, the change of simultaneous flowering of the species increases northwards due to a more variable climate and higher altitudinal variation. Compared with conifers, the reproduction cycles of the two birch species were found to be well protected from damage by frost.
At the beginning of the investigation period the total biomass of the Scots pine (Pinus sylvestris L.) stands on the ordinary sedge pine mire was 48 t/ha. The biomass of the mixed stands of Scots pine and birch (Betula pubescens Erhr.) on the herbrich sedge pine mire was 91 t/ha, out of which 60% was from pine. The biomass of the Norway spruce (Picea abies (L.) H. Karst.) on the Vaccinium-Myrtillus spruce mire was 148 t/ha. The average annual net increment of the stand biomass was 5.8 t/ha in the unfertilized pine stand and 6.7 t/ha in the NPK and micronutrient fertilized one during the six-year investigation period. The corresponding figures in the mixed stand were 7.2 t/ha and 7.6 t/ha. The net increment of the biomass in the unfertilized spruce stand was 6.9 t/ha and in the fertilized 8.4 t/ha. A considerable proportion of the net increment was lost to the ground as litter in all stands.
The nitrogen, phosphorus, potassium, magnesium, iron, manganese, zinc, copper and boron cycles were investigated. The annual nitrogen uptake from the soil was 26–42 kg/ha, that of phosphorus 2.5–3.4 kg/ha, potassium 4.5–12 kg/ha, calcium 12–29 kg/ha, magnesium 2–4 kg/ha, iron 1.4–6.6 kg/ha, manganese less than 2 kg/ha and the other nutrients only some grams. Only part of the fertilized nutrients was fixed in the stand.
The PDF includes a summary in Finnish.
Mixed forests are known for their ability to provide a wide range of ecosystem services. Such forests have higher biodiversity compared to monocultures, are resilient against disturbances and may mitigate the effects of climate change. Despite well-known benefits, there is still little information on how these forests should be established and managed. The aim of this study was to describe the early growth dynamics of current boreal young mixed stands of planted Norway spruces (Picea abies (L.) Karst.) and naturally regenerated birches (Betula spp.). We collected data from 9 stands planted for spruce 8–14 years ago in Southern and Central Finland. Stem analysis was conducted to 144 spruces and to 144 birches to determine previous growth. We modelled the height and diameter development of individual trees in relation to tree age at stump height using non-linear mixed Chapman-Richards model. There were no significant differences between spruce and seed-origin birch in diameter growth at stump height, but the initial height increments of natural birches were larger than those of planted spruces. However, planted spruces were able to keep up with the height development of birches, if spruces received a head start over naturally regenerated seed-origin birch for two growing seasons. Thus, naturally regenerated birch admixture can be utilized to establish single-storied spruce-birch mixtures, and the admixture should be retained during the early cleaning of planted spruce stands.
Timber production and profitability were evaluated for spontaneously-regenerated mixtures on two formerly clearcut areas. The abandoned areas developed into birch-dominated (Betula pendula Roth and Betula pubescens Ehrh.) stands with successional ingrowth of Norway spruce (Picea abies (L.) H. Karst.). An experiment with randomized treatments within blocks was established, using three management strategies and one unthinned control, resulting in variation in optimal rotation age, merchantable volume and species composition. The management strategies were evaluated based on total production (volume) by using measured growth data 42 years after clearcutting and the modelled future stand development. The long-term effects of spontaneous regeneration and management strategies were evaluated based on land expectation value (LEV) and compared with a fifth management strategy using artificial regeneration and intense thinnings. 12 years after treatment, at a stand age of 42 years, the unthinned control had produced the highest total stem volume. At interest rates of 2% or higher, the unmanaged forest was an economically viable strategy, even compared to an intensive management strategy with a preferred merchantable timber species. Interest rates clearly impacted the profitability of the different management strategies. This study shows that when spontaneous regeneration is successful and dense, the first competition release can have a high impact on the development of future crop trees and on the species mixture.
The aim of this study was to develop individual-tree diameter and height growth models for Scots pine, Norway spruce, and pubescent birch growing in drained peatlands in Finland. Trees growing in peatland sites have growth patterns that deviate from that of trees growing in mineral soil sites. Five-year growth was explained by tree diameter, different tree and stand level competition measures, management operations and site characteristics. The drainage status of the site was influencing growth directly or in interaction with other variables. Site quality had a direct impact but was also commonly related to current site drainage status (need for ditch maintenance). Recent thinning increased growth of all species and former PK fertilization increased growth of pine and birch. Temperature sum was a significant predictor in all models and altitude for spruce and birch. The data were a subsample of the 7th National Forest Inventory (NFI) sample plots representing northern and southern Finland and followed by repeated measurements for 15–20 yrs. Growth levels predicted by the models were calibrated using NFI11 data to remove bias originating from the sample of the modelling data. The mixed linear models technique was used in model estimation. The models will be incorporated into the MOTTI stand simulator to replace the current peatlands growth models.
The main aim of the current study was to estimate the annual net nitrogen mineralization (NNM) flux in stands of different tree species growing on drained peatlands, as well as to clarify the effect of tree species, soil properties and litter on annual NNM dynamics. Three study sites were set up in May 2014: a downy birch (Betula pubescens Ehrh.) stand and a Norway spruce (Picea abies (L.) Karst.) stand in Oxalis full-drained swamp (ODS) and a Scots pine (Pinus sylvestris L.) stand in Myrtillus full-drained swamp (MDS). The NNM flux was estimated using the in situ method with incubated polyethylene bags. The highest value of NNM was found in stands that were growing on fertile ODS: 127.5 kg N ha–1 yr–1 and 87.7 kg N ha–1 yr–1, in the downy birch stand and in the Norway spruce stand, respectively. A significantly lower annual NNM flux (11.8 kg N ha–1 yr–1) occurred in the Scots pine stand growing in MDS. Nitrification was highest at fertile ODS sites and ammonification was the highest at the low fertility MDS site. For all study sites, positive correlation was found between soil temperature and NNM intensity. The difference in annual NNM between the downy birch stand and the Norway spruce stand growing on similar drained fertile peatlands was due to litter quality. The annual N input into the soil through leaf litter was the highest at the downy birch site where also the C/N ratio of litter was the lowest. The second highest N input into the soil was found in the spruce stand and the lowest in the pine stand.
Downy birch (Betula pubescens Ehrh.) stands on drained peatlands are often considered useless because they typically do not yield good-quality sawn timber. However, covering an area of ca. 0.5 million hectares and with total yields of up to 250 m3 ha–1, downy birch stands on peatlands in Finland have a potential for pulpwood and/or energy wood production. We examined the financial performance of alternative management regimes (with or without thinnings, different thinning intensities, several rotation lengths) combined with alternative harvesting methods (pulpwood, energy wood, or integrated, energy wood being delimbed stems or whole trees). We used data from 19 experimental stands, monitored for 20–30 years. For harvesting removals we considered both actual thinning removals and final-cutting removals with alternative timings that were based on the monitoring data. We assessed the profitability as a combination of the net present value of the birch generation and the bare land value of future generations of Norway spruce (Picea abies (L.) Karst.). The most profitable management was growing without thinnings until whole-tree final cutting at the stand age of 40–45 years with an advanced multi-tree harvesting method. In contrast, the standard method in whole-tree final cutting resulted in the lowest profitability, and an integrated method with the energy wood as delimbed stems was the best of the standard methods. Thinnings were unprofitable especially when aiming to produce energy wood, whereas aiming for pulpwood, light precommercial thinning was competitive. Commercial thinning at the traditional “pulpwood stage” had little effect on profitability. The best stand age for final cutting was 40–65 years – earlier for very dense stands and whole-tree energy wood harvesting with advanced method, later for precommercially thinned stands and pulpwood harvesting.