Dormant needles from 129 Norway spruce (Picea abies (L.) H. Karst.) trees from the 2nd and 3rd topmost whorls were collected from spruce stands locating fairly close to each other. Tree height varied from 8 to 25 metres. Trees with and without visual potassium deficiency symptoms in needles were selected and analysed for nitrogen, phosphorus, potassium, magnesium, boron, copper, zinc, and 3 free polyamines putrescine, spermine and spermidine.
The concentrations of all the analysed nutrients ranged from deficient to satisfactory levels. Free putrescine, spermidine and spermine concentrations in the current needles had a wide variation between the trees. Spermidine had a positive and spermine a negative correlation with potassium. Putrescine had a strong negative correlation with potassium with statistically significant increase in putrescine starting at potassium concentrations below 5.4 mg/g dry weight. The regression between putrescine and potassium changed from a linear to a non-linear form at the potassium concentration of 4.2–4.6 mg/g dry weight representing a severe K deficiency limit. The corresponding K/P ratio was 2.6–2.7. Extremely low phosphorus concentrations (P < 1.0 mg/g) lowered putrescine concentrations, but otherwise the relationships between putrescine, spermidine or spermine and potassium concentrations were unaffected by tree nutrition. At adequate potassium levels the putrescine concentrations were only slightly lower in trees taller than 20 metres than in trees of 8–16 metres height. The results show that the needle putrescine concentration can be used quite reliably for describing potassium nutrition of Norway spruce in varying nutritional and tree size conditions.
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 purpose of this article was to collate the literature on fungal diseases that occur on seedlings in forest nurseries. It describes the symptoms of the diseases, the infection pattern of each fungus and the possibilities of controlling the diseases. As background a short introduction is given on forests and nursery practices in Finland.
The purpose of this study was to compare the Weibull distributions estimated for the entire growing stock of a stand and separately for Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) in describing the basal area diameter distributions in mixed stands. The material for this study was obtained by measuring 553 stands located in eastern Finland. The parameters of the Weibull distribution were estimated using the method of maximum likelihood. The models for these parameters were derived using regression analysis. Also, some parameter models from previous studies were compared with the measured distribution. The obtained distributions were compared using the diameter sums of the entire growing stock, diameter sums by tree species and of the sawtimber part of the growing stock. The results showed that far more accurate results were obtained when the distributions were formed using parameter models separately for the different tree species than when using parameter models for the entire growing stock. This was already true when considering the entire growing stock of the stand and especially when the results were examined by tree species. When the models for the entire growing stock were applied by tree species in relation to basal areas, the results obtained were overestimates for Norway spruce and underestimates for Scots pine. The models from earlier studies, where parameter models were estimated separately for tree species from the National Forest Inventory data, showed good fits also in regard to the data of this study.
The prefire fungal flora (polypores and corticoid fungi) of 284 dead trees, mainly fallen trunks of Norway spruce (Picea abies (L.) H. Karst.), was studied in 1991 in an old, spruce-dominated mesic forest in Southern Finland. Species diversity of the prefire fungal flora was very high, including a high proportion of locally rare species and four threatened polypore species in Finland.
In 1992 part of the study area (7.3 ha) was clear-cut and a 1.7 ha forest stand in the centre of study area was left standing with a tree volume of 150 m3/ha, and later on (June 1st) in the same year the whole area was burned. Burning was very efficient and all trees in the forest stand were dead one year after the fire. Also, the ground layer burned almost completely.
In 1993 the fungal flora of the 284 sample trees was studied again. Most of the trees had burned strongly and the fungal species diversity and the evenness in community structure had decreased considerably as compared with the prefire community. Species turnover was also great, especially in corticoid fungi. Greatest losses in the species numbers occurred in moderately and strongly decayed trees, in coniferous trees and in very strongly burned trees. Fungal flora of non-decayed and slightly decayed trees, deciduous trees and slightly burned trees seemed to have survived the fire quite well, and in these groups the species numbers had increased slightly as compared with the prefire community.
Fungal species suffering from fire (anthracophobe species) were mainly growing in moderately and strongly decayed trees before the fire, whereas species favoured by fire (anthracophile species) were growing in less decayed trees. No fruitbodies of threatened polypores or other "old-forest species" of polypores were found again after fire. Some very common and effective wood-rotting fungi (e.g. Fomitopsis pinicola, Fomes fomentarius, Antrodia serialis) survived the fire quite well (anthracoxene species). Species favoured by fire were mainly ruderal species which can utilize new, competition-free resources created by fire, and species that have their optima in dry and open places also outside forest-fire areas. Some rarities, e.g. Phanerochaete raduloides and Physisporinus rivulosus, were favoured by fire.
The horizontal and vertical stand structure of living trees was examined in a managed and in a primeval Norway spruce-dominated forest in Southern Finland. Tree size distributions (DBHs, tree height) were compared using frequency histograms. The vertical distribution of tree heights was illustrated as tree height plots and quantified as the tree height diversity (THD) using the Shannon-Weaver formula. The horizontal spatial pattern of trees was described with stem maps and quantified with Ripley's K-function. The spatial autocorrelation of tree sizes was examined with semivariogram analysis. In the managed forest the DBH and height distributions of trees were bimodal, indicating a two-layered vertical structure with a single dominant tree layer and abundant regeneration in the understory. The primeval forest had a much higher total number of trees which were rather evenly distributed in different diameter and tree height classes. The K-function summaries for trees taller than 15 m indicated that the primeval stand was close to complete random pattern. The managed stand was regular at small distances (up to 4 m). The semivariograms of tree sizes (DBH tree height) showed that the managed forest had a clear spatial dependence in tree sizes up to inter-tree distances of about 12 meters. In contrast, the primeval spruce forest had a variance peak at very short inter-tree distances (< 1 m) and only weak spatial autocorrelation at short inter-tree distances (1–5 m). Excluding the understory trees (h < 15 m) from the analysis drastically changed the spatial structure of the forest as revealed by semivariograms. ln general, the structure of the primeval forest was both horizontally and vertically more variable and heterogeneous compared to the managed forest. The applicability of the used methods in describing fine-scale forest structure i discussed.
To project the changes in wood production of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) in Finland as a result of climate change, two separate studies were made. The first study, at the Faculty of Forestry, University of Joensuu, based its projections on mathematical models; the second one, at the Finnish Forest Research Institute, based projections on measurements of wood production in two series of aged provenance experiments. The results of the two studies were similar for both species: after a 4°C increase of the annual mean temperature a drastic increase in wood production in northern Finland, but little effect, or even some decrease in the southern part of the country. However, the assumptions used in the two studies differed. One important difference was that in the models the temperature is assumed to be increasing gradually over the years, whereas in the provenance experiments, climate changed immediately when the seedlings were transferred to the planting sites. Another problem with the provenance experiments is that when material is moved in a north-south direction in Finland, not only temperature but also photoperiod changes markedly. To compare these two studies, site factors (e.g. soil type, temperature, precipitation) and silvicultural factors (e.g. plant spacing, survival, time of thinning, thinning intensity) from the provenance experiments were included a variable in the mathematical models.
A total of 1,800 3-year old seedlings of Norway spruce (Picea abies (L.) H. Karst.) from two Norwegian and one German provenance were treated with two different nitrogen levels during the 1992 growth season. The plants were kept during the following winter at two different temperature levels. In the spring of 1993, the nutrient application was resumed, and the plants were divided between three different treatments, 350 and 650 p.p.m. in open top chamber and a control plot outside the chambers. This treatment was repeated also during the following 1994 growth season.
The growth and primary production were studied by photosynthesis experiments and by non-destructive growth measurements. The result indicate that raised winter temperature may lead to increased needle loss and reduced growth the following season, particularly in northern provenances. Carbon dioxide significantly influenced growth in addition to nutrient level and winter temperature. High CO2 also seemed to cause increased photosynthesis at early season, and earlier budbreak and growth cessation than in control plants.
The effect of species mixture was studied in a mixed stand of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) by simulating around 100 different treatment schedules during the rotation in a naturally regenerated even-aged stand located on a site of medium fertility in North Karelia, Finland. Both thinning from below and thinning from above were applied. Optimum rotations were determined by maximising the net present value calculated to infinity and different treatment schedules were compared with the net present value over one rotation as per rotation applied. In the optimum treatment programme, the proportion of pines was decreased by half of the basal area in the first thinning stage and by the end of the rotation to about one third. In thinning from above, the proportion of pines can be maintained at a slightly higher level. It is economically profitable to maintain the growing stock capital at approximately the level recommended by Forest Centre Tapio, a semi-governmental forestry authority. With non-optimum species composition, the loss in net present value over one rotation can be about 10 % in thinning from below and about 20 % in thinning from above.
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.
Germination of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) pollen decreased during exposure to open air conditions. Usually more than half of the pollen remained germinative after a few days outdoors, but following more than four days outdoors the germination became very low. This study supports the opinion that pollen in the atmosphere remains viable long enough to allow for long-distance gene flow by pollen migration, as an important factor in genetic management of conifers and in evolution, maintaining diversity and potential for adaptation.
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.
Independent of genotype, increased spacing results in increased branch diameter of Scots pine (Pinus sylvestris L.), but on different levels for different genotypes. Frequency of defects like spike knots and crooked stems are under stronger genetic than silvicultural control. Simultaneous improvement of rate of growth and timber properties is feasible. Deteriorating of both factors can happen rapidly at a negative selection. A defect like stem cracking of Norway spruce (Picea abies (L.) H. Karst.) only manifests itself under drought stress when certain genetic and environmental prerequisites are present, like high fertility and wide spacing. This emphasize the fact that new silvicultural methods may reveal genetic weaknesses.
Temperature sums required for budburst in various Norway spruce (Picea abies (L.) H. Karst.) provenances were determined, and weather statistics were then used to predict the risk of potentially damaging frosts at 11 locations in Sweden. Frost risk was quantified as the probability of a frost occurring within 100 day-degrees (two weeks) after budburst. The examples provided show that a spruce seedling from central Sweden has to sustain almost twice as many frost occassions as a seedling from Belorussia, when planted in southern and central Sweden. The method presented here can be used for mapping early summer frost risk in Sweden and for supporting provenance transfer guidelines.
Seedlings of Picea abies (L.) H. Karst. full-sib families of contrasting origins were cultivated in a phytotron under different photoperiodic, light-intensity and temperature treatments during their first growth period. The effects of the treatments on juvenile growth traits – whether enhanced or delayed maturation was induces – were observed during the two subsequent growth periods. The following hypotheses were tested: (A) Enhanced maturation can be induced in the first growth period from sowing with (i) a long period of continuous light during active growth (24 weeks vs. 8 weeks); (ii) a shorter night during bud maturation (12 h vs. 16 h); high temperature (25°C vs. 20°C) during (iii) active growth, growth cessation and bud maturation; and during (iv) the latter part of growth cessation and bud maturation only. (B) Delayed maturation can be induced after (i) low light intensity during growth cessation and bud maturation (114 μmol m-2 s-1 vs. 340 μmol m-2 s-1); low temperature (15°C vs. 20°C) during (ii) active growth, growth cessation and bud maturation; and during (iii) the latter part of growth cessation and bud maturation only.
The most dramatic effect was observed after 24 weeks of continuous light during active growth. All traits showed a significantly more mature performance in the second growth period compared with the control. The effect for all but one trait was carried over to the third growth period. This is in accordance with the hypothesis that the activity of apical shoot meristems controls the maturation process. For the other treatments there was only weak or no support for the hypothesis of induction of enhanced or delayed maturation. Strong family effects were observed for all traits. Differential responses of the various latitudinal families were observed, suggesting that family effects must be considered to predict and interpret correctly how plants will respond to environmental effects.
53 genotypes of embryonal suspensor masses (ESMs) rescued from mature seeds of Norway spruce (Picea abies (L.) H. Karst.) were examined for their pattern of growth and development under standardized culture conditions in vitro. Patterns were classified according to the colour of the colonies grown in darkness, clarity of cell masses and proembryos in the mucilaginous ESM, surface boundary topology of colonies, structure of suspensors, growth rate of the ESM, and recovery of mature embryos.
Five distinctive major growth patterns were observed among ESM colonies under standardized culture conditions. The multiplication of proembryos and early embryos by cleavage and budding polyembryony was the main factor contributing to proliferation and colony growth and further determined the morphology of the colonies. Callus and teratological structures were induced from early embryos by changing the standardized culture conditions i.e. inadequate subculture, excessive dose of 2,4-D in the medium and premature exposure of the colonies to light. Results enable the selection of ESM genotypes for the predictable recovery of mature somatic embryos.
The survival of forest tree species in wildfires was examined on two burned stands. Norway spruce (Picea abies (L.) H. Karst.) and birches (Betula spp.) proved to be sensitive to the effects of wildfire; almost all individuals of these tree species were killed by the fires. Scots pine (Pinus sylvestris L.) was more tolerable to the effects of wildfire; i.e. one out of five Scots pines survived. Fire tolerance increased as tree size increased.
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Mixed linear models were constructed to describe the height development of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) advance growth after release cutting. The models related density of the overstory, time elapsed since release cutting and tree size with annual height increment. Parameters of preliminary models were estimated from a limited data set to judge the feasibility of the approach for further studies.
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Seedlings from four Norway spruce (Picea abies (L.) H. Karst.) stands originating from areas with effective temperature sums ranging from 710 d.d. to 1,150 d.d. were raised under artificial light and temperature treatment. After a 10-week growing period the hardening process was started by subjecting the seedlings to +8°C night temperature and +15°C day temperature, and increasing the night length by 1.5 hour/week. Hardiness was measured by means of artificial freezing treatment (-10°C or -15°C), followed by visual estimation of the degree of needle injury. The stem height, lignification and bud development were measured before the freezing treatment. The amount of injury increased the more southern the origin of the tested material was. Furthermore, the proportion of non-lignified part of the seedling stem was negatively correlated with the latitude of the provenances. The proportion of seedlings with clearly visible buds was more than 90% in the northernmost entry and less than 1% in the southernmost one. The overall correlation coefficient between the needle injuries and the proportion of non-lignified part of the stem was rather high, but varied considerably from 0.3 in the northernmost material to over 0.6 in the southern provenances. According to the results, it seems to be possible to use growth characteristics as an indicator of frost hardiness at the provenance level.
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The paper gives an introduction of the tree breeding program of Sweden that started in 1936 by the establishment of an association for the tree breeding. In 1967 the Institute of Forest Improvement was founded and it replaced the earlier association. The main species in the programme have been Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.), lately also birch (mainly Betula pendula Roth.) and lodgepole pine (Pinus contorta). In addition, limited breeding has been done also with hybrid aspen (Populus tremula x P. tremuloides), oak (Quercus), larch (Larix), black spruce (Picea mariana) and a few other native and exotic species. The dominating initial effort has been to select plustrees in natural stands and use them for production of reforestation material. In addition, a considerable body of tests was built. The paper lists the status of breeding material of the different tree species and introduces the medium and short-term breeding programmes.
Crown characteristics and the distribution of three years’ (1986–88) biomass production of 20 pendulous Norway spruce (Picea abies f. pendula (Lawson) Sylvén) trees with heritable narrow crown and 15 normal-growned spruces (Picea abies (L.) H. Karst.) were studied in a 19-year-old mixed stand.
The form of the crown is conical in normal-crowned trees, columnar and narrow in pendulous trees. The partitioning of aboveground biomass to stems during the studied 3-year period was significantly higher in pendulous (0.281) than in normal-crowned trees (0.255) and also the ratio between growth of stemwood and growth of needle biomass during three years was higher in pendulous trees (0.67 g g-1) than in normal-crowned trees (0.52 g g-1). The needle biomass was distributed higher in the crown in pendula than in normal-crowned trees and they had a higher needle biomass/branchwood biomass ratio than normal trees. The difference in harvest increment between the two crown types are mostly due to the significantly lower branchwood biomass values in pendulous than in normal-crowned trees. The higher needle ’efficiency’ in pendulous trees is probably connected with high partitioning of needle biomass to the upper part of the crown in pendulous trees.
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The effect of photon flux density on bud dormancy release in two-year-old seedlings of Norway spruce (Picea abies (L.) H. Karst.) was examined. The seedlings were first chilled for 0–21 weeks under natural conditions and then forced in a warm greenhouse either in low (15 μEm-2s-1) or in high (300 μEm-2s-1) photon flux density. Occurrence of bud burst was observed in the forcing conditions, and the observations were used for estimating the cumulative frequency distribution of the chilling requirement for growth competence. The estimated distribution had greater variance in the low photon flux density than in the high photon flux density forcing. This finding suggests that unnaturally low photon flux densities during forcing may yield overestimates of the genetic within-population variation in the chilling requirement for growth competence.
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Shoot losses due to maturation feeding by pine shoot beetles (Tomicus piniperda (L.) and T. minor (Hart.), Col., Scolytidae) and subsequent growth losses were studied in Scots pine (Pinus sylvestris L.) stands growing at different distances from a timber yard, where pine timber was stored during the years 1982–84. In autumn 1985, pine trees were felled at 20, 40, 80, 500 and 1,500 m distance from the timber yard, five trees in each distance class. Trees were analysed for beetle attack, needle biomass and growth. In autumn 1988, increment cores were taken from 20 trees in each distance class.
In 1985, different damage estimates showed that beetle damage was more than 10-fold in the crowns of pine trees growing close to the timber yard as compared to less damaged trees in greater distance. Crude needle biomass estimates indicated that the trees attacked most had lost more than half of the total foliage. Following three years of attack, basal area growth decreased for 2–3 years and recovered during the subsequent 3 years, the total period of loss thus being 5–6 years. The loss in volume growth during 1983–85 was ca. 70, 40, 20 and 10% at 20, 40, 80 and 500 m distance from the beetle source, respectively, compared to the stand at 1,500. Growth losses did not occur until the number of beetle-attacks, ”pegs”, exceeded ca. 200 per tree. The highest observed growth losses occurred in trees with more than 1,000 pegs per tree.
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The simulation model consists of a method to generate theoretical Norway spruce (Picea abies (L.) H. Karst.) stands, and a spatial growth model to predict the growth of these stands. The stand generation procedure first predicts the tree diameters from a few stand characteristics and from tree locations. Tree age and height are predicted using spatial models. Spatial growth models were made for both diameter growth and basal area growth. Past growth was used as a predictor in one pair of models and omitted in another pair. The stand generation method and the growth models were utilized in studying the effect of tree arrangement and thinning method on the growth of a Norway spruce stand.
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Different methods of sowing and planting of Norway spruce (Picea abies (L.) H. Karst.) were compared on fertile sites in North Karelia (62°20’N, 29°35’E, 85–120 m a.s.l.). The planting material were 4-year-old bare-rooted transplants, 2-year-old bare-rooted seedlings, and 2-year-old containerized seedlings raised in plastic greenhouse. The sowing methods were band sowing and shelter sowing. Ground vegetation was controlled during the first growing season mechanically or chemically, or the control was omitted totally.
Planting of spruce gave better results than sowing. After eight growing seasons there were sowed seedlings left in 30% of the sowing pots. The average height of them was 35 cm. Seedling survival was best with large bare-rooted transplants (91%). Survival of containerized seedlings was 79% and of small bare-rooted transplants 71%. The average height of large bare-rooted transplants was 131 cm, of containerized seedlings 86 cm and small bare-rooted seedlings 68 cm.
Sowing is not an advisable method for regeneration of spruce due to the small survival rate and slow initial development when ground vegetation is controlled only once. Also 2-year-old seedlings gave a satisfactory result in regeneration. Seedlings raised in greenhouse were more sensitive to frost damage than seedlings grown on open ground.
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The effect of three pesticides containing either dimethoate (0.5% a.i.), permitrin (0.5%) or triadimephon (0.5%) on the cone pests and flowering biology of Norway spruce (Picea abies (L.) H. Karst.) was tested in a seed orchard in mid-May or in the beginning of June. The pesticide treatments significantly reduced infestation by Laspeyresia strobiella and Kaltenbachiella strobi only. Variation in the number of cones infested by both insects and cone rusts was high between the spruce clones. Generally, the pesticides did not affect flower viability, seed quality or seed germination, but reduced drastically the germination capacity of pollen in vitro. In practice, sufficient control cannot be achieved with concentrations or methods used in the present study.
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Effect of dolomite lime and wood ash (0, 0.5, 1, 2, 4, 8 and 16 kg m-3) on the chemical composition of low humified Sphagnum peat was studied. Germination of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.) and silver birch (Betula pendula Roth) and the subsequent growth of these seedlings were investigated in a greenhouse experiment. Nutrient concentrations in shoots and roots of pine seedlings were also analysed. The pH of peat increased asymptotically from 3.8 to about 7.0 with increasing lime regimen and to about 8.0 with increasing ash regimen. Wood ash linearly increased electrical conductivity and P, K, and Ca concentrations of peat. Rate of germination, within 7 days, of pine and spruce was best at low pH (<5) while birch seeds had a slightly higher pH optimum (4–6). Germination capacity, within 21 days, was not affected by pH or application regimen of either lime or ash. Pine and spruce seedlings grew best with lime and ash doses of 0.5–2.0 kg m-3, the pH of peat being 4–5. Lime and ash treatments did not affect the growth of birch seedlings, but wood ash increased nutrient concentration of pine seedlings.
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The results of regenerating 54 and 36–38-year old strip cuttings were surveyed in the Kivalo Research Forest (N 66°20’, E 26°40’). 15 measurement plots were placed on each strip. The most common forest type was Hylocomnium-Myrtillus type. Regeneration of the strips proved to be slow. Most of the spruces growing on the strips probably originated from the time before the cutting. The average number of stems was 1,155 per ha, of which one third consisted of broadleaved trees. The average volume increment of stem wood after cutting had been about 1 m3/ha/yr, but it was increasing at the time of the inventory. Both the reforestation of the strips and the development of the emergent stands were dependent on elevation and site fertility. Site fertility was indicated by the abundance of Vaccinium myrtillus.
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Seed mass within any plant species is one of the least plastic components of plant structure. The aim of this study was to analyse the variation in the seed mass of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) in relation to three environmental factors: soil fertility, mean temperature and precipitation during seed filling period. Data published earlier on seed mass of these species on different sites and different years was used in the study.
The seed mass of both species was independent of soil fertility (forest type) but did vary between different years. It is hypothesized that if the seed-ripening summer is warmer than average, Scots pine seed mass tends to be smaller. In this study, seed mass varied independently of the amount of precipitation during the ripening summer. However, generalization of the results requires further study.
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The author first introduced the cut-block seedling production method to Finland in 1969. The aim is to raise seedlings whose lateral roots do not become deformed as a result of a restricting container or other external pressure. The seedlings are raised in a large, fairly compact substrate block where the roots can freely develop in a normal fashion. The blocks are then cut up into individual cubes, each containing a seedling. The precise positioning of the sowing point permits mechanization of the work.
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The paper continues an earlier study by Kilkki and Päivinen concerning the use of the Weibull function in modelling the diameter distribution. The data consists of spruces (Picea abies (L.) H. Karst.) measured on angle count sample points of the National Forest Inventory of Finland. First, maximum likelihood estimation method was used to derive the Weibull parameters. Then, regression models to predict the values of these parameters with stand characteristics were calculated. Several methods to describe the Weibull function by a tree sample were tested. It is more efficient to sample the trees at equal frequency intervals than at equal diameter intervals. It also pays to take separate samples for pulpwood and saw timber.
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A survey was conducted in Finland in 1988 to determine whether the pine wood nematode Bursaphelenchus mucronatus Mamiya & Enda 1979 (Nematoda: Aphelenchoididae) or the closely related species B. mucronatus would occur in Finnish forests. Dead or dying standing trees and timber of two conicer species, Pinus sylvestris L. (Scots pine) and Picea abies (L.) H. Karst. (Norway spruce) were analysed for the presence of these nematodes. Monochamus spp. pine sawyers (Coleoptera: Cerambycidae) were also collected and inspected for the presence of dispersal fourth juvenile stages (dauerlarva) of the nematodes. The species B. xylophilus was not found, but B. mucronatus appeared to be widespread in the country. Individuals of this nematode were found both from Scots pine and Norway spruce. Adults of two Monochamus species were found, M. galloprovincialis and M. sutor. Only two of the examined beetles of the former species had dauerlarvae in their body.
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Models concerning the effects of temperature on dormancy release in woody plants were tested using two-year old seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.). Chilling experiments suggest that the rest period has a distinct end point. Before the attainment of this end point high temperatures do not promote bud development towards dormancy release, and after it further chilling does not affect the subsequent bud development. A new hypothesis of dormancy release is suggested on the basis of a comparison between present and earlier findings. No difference in the proportion of growth commencing seedlings were detected between the forcing temperatures of 17°C and 22°C. The rest break of 50% of Norway spruce and Scots pine seedlings required six and eight weeks of chilling, respectively. Great variation in the chilling requirement was found, especially for Scots pine.
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Frost resistance during shoot elongation in seedlings of Norway spruce (Picea abies (L.) H. Karst.) was studied in two experiments. The aim of the first study was to evaluate the effect of varying mineral nutrition. Except for potassium, only minor differences in mineral elements concentrations were established, presumably due to low levels of irradiance and thus a low rate of dry matter production. No significant differences in frost injuries were found between the treatments in the experimental series, but the control seedlings were significantly less injured. It is assumed that poor hardiness development at the end of one growth period resulting from low levels of irradiance may decrease the frost resistance during the next shoot elongation phase. Observations from the second experiment with Norway spruce nursery stocks representing different seedling ages and production systems, support this assumption.
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Nursery grown Norway spruce (Picea abies (L.) H. Karst.) seedlings from 12 different seed orchards were tested for early autumn frost hardiness using artificial freezing tests. Seed orchards containing grafted parent clones originating from high altitudes produced seedlings showing higher damage than commercial control seed lots of the commercial controls. A seed orchard containing both German and Norwegian clones produced seedlings showing high damage. The correlation between bud-set and frost damage was high at the provenance level, but lower at the half- and full-sib-levels. Families with good growth capacity in progeny field tests showed large between-family variation in frost damage in the artificial freezing tests. This indicates the possibility to combine high growth rate with acceptable autumn frost hardiness in the selection of parent trees.
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Visible frost damage to forest trees in Sweden seldom occurs in winter but is frequent in late spring, summer and early autumn. Frosts are frequent in all seasons in various parts of Sweden, even in the southernmost part (lat. 56°, N) and temperatures may be as low as -10°C even around mid-summer. Ice crystal formation within the tissues, which in most seedlings takes place at around -2°C, causes injury, not the sub-zero temperatures themselves.
The apical meristem, the elongated zone, and the needles of seedlings of Picea abies (L.) H. Karst. in a growing phase were damaged at about -3°C and those of Pinus sylvestris L. at about -6°C. Other species of the genus Pinus were tested and most were found to be damaged at about -6°C, with some variations. Picea species tested were damaged at about -3°C to -4°C.
A method has been designed to compare the response of different species to winter desiccation, which occurs under conditions of (1) low night temperature, (2) very high irradiation and increase in needle temperature during the photoperiod, (3) frozen soil, and (4) low wind speed. There were differences in response to winter desiccation between pine and spruce species. Seedlings of Pinus contorta tolerated these winter desiccation conditions much better than those of P. sylvestris or Picea abies. Picea mariana was the least tolerant of the species tested.
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The study material consisted of 13 rather old Norway spruce (Picea abies (L.) H. Karst.) and 17 Scots pine (Pinus sylvestris L.) stands located in different parts of Finland. In each stand the seed crops, radial growth and amount of latewood were measured during a period of about ten years. Seed production reduces the radial growth of spruce and pine in the year of seed maturing. In Southern and Central Finland also the proportion of latewood is reduced. Seed production accounts for about 14% of the variation in radial growth of a spruce stand growing in Lapland, and 27% in other parts of Finland. In pine stands the seed crop explains 19% of the variation in radial growth in Lapland, and only 7% in the rest of Finland. In spruce stands an average seed crop reduces radial growth by 14% in Lapland and 5% in the rest of the country. An abundant seed production causes a reduction of about 20%. In southern parts of Finland, the proportion of latewood is reduced by 5% in an average seed year and by 24% in a good seed year. In pine stands an average seed crop decreases the width of annual ring by 5%, and a good seed crop by 15%. Outside Lapland, also the proportion of latewood is reduced: in an average seed year by 5%, and in a good seed year by 16%. The reduction in volume growth of spruce stands due to an average seed crop was estimated to be about 10% in Lapland, and 6% in other parts of Finland. A prolific seed production causes a reduction of 20%. In old pine stands the reduction is 5% in an average seed year, and 15% in a good seed year.
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The seed crop of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) is predicted with the help of mean monthly temperatures during May–August one and two years before the flowering year. The prediction models were made separately for Lapland and for the rest of Finland. The models are based on 10-year periods of seed crop measurements and climatic data. The total number of time series was 59.
In Lapland, Norway spruce flowered abundantly and produced an abundant seed crop after warm July–August and two years after cool July–August. In other parts of Finland, warm June and July produced a good flowering year, especially if these months were cool two years before the flowering year.
In Lapland, Scots pine flowered abundantly if the whole previous growing season was warm. Elsewhere in Finland, a cool June preceded prolific flowering in the coming year if the rest of the growing season was considerably warmer than the average.
The prediction models explained 37–49 % of the variation in the size of the seed crop. The occurrence of good and poor seed years was usually predicted correctly. Using the presented models, the prediction of the seed crop is obtainable 1.5 year for Norway spruce and 2.5 year for Scots pine before the year of seed fall.
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In laboratory studies the heartwood content seems to be the only natural property of a wood of different tree species influencing the decay resistance. Moistening and drying by diffusion happen quite slowly. Scots pine (Pinus sylvestris L.) sapwood takes moisture by capillary action quicker than pine heartwood and Norway spruce (Picea abies (L.) H. Karst.) wood. Swelling and shrinkage are also greatest in pine sapwood. Impregnation of pine sapwood can give it better hydrophobic and dimensional stability than that of pine heartwood.
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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 mathematical model was developed for determining the value of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.) stems on the basis of sawing and pulping. The model was based on selling prices of sawn goods, pulp and other products as well as processing costs. Sawing was applied to large-dimension parts of stems and pulping to other parts and small stems. Bark and other residues were burned. The quality of pine stems was described by the distance of the lowest dead branch. In spruce only stem size affected the quality-
According to the results, the size of stem affects considerably the value of pine stems and clearly that of spruce stems. The main reason is an increase in the productivity of frame sawing as the stem size increases. In pine another factor is the higher price of sawn goods. The effect of pulp price increases as the stem size decreases. Even in large sized stems the effect of pulp was notable as the value of chips and saw dust was determined on the basis of product values in export. The competition ability of mechanical pulp was greatly affected by the price of electricity.
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A computer model was developed for predicting knottiness of wood material of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.) and birch (Betula sp). The prediction included location of knots, their size and quality, i.e. if they are dead or living knots. The model suits best for tree species where branches are born at the base of shoots, in Finland such tree species is Scots pine.
The usefulness of the model was tested in the prediction of knots in wooden elements of joinery industry. According to the results, the shape of cross section affects the surface quality of elements. Especially useful is a quadratic cross section as it increases the probability to get a knotless surface.
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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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A method for calculation of the effect of practical fertilization for economic evaluation is presented and discussed. 55 Norway spruce (Picea abies (L.) H. Karst.) dominated stands on Oxalis-Myrtillus type sites were surveyed five to eight years after fertilization with nitrogen (90-170 kg/ha). The relationships between the fertilization effect and various stand characteristics were discussed. Fertilization increased the growth of the stands on an average by 2.2 m3/ha/year. In total the increase of tree growth during the research period was 17.5 m3/ha. This corresponds to a yield of 525–659 FIM/ha.
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Early growth of four different tree species (Pinus sylvestris L., Picea abies (L.) H. Karst., Larix sibirica Ledeb and Betula pendula Roth) 16–23 years after planting were compared in a field experiment of 16 square plots established on a stony, grove-like upland (Oxalis-Myrtillus forest type) in Southern Finland. This study gives additional results to the publication Folia Forestalia 386/1979.
At this early stage, the growth of the spruce stand was clearly slower than that of the other species for all parameters to be measured (height, diameter, and volume growth). Height growth was most rapid in the silver birch stand and diameter growth in the larch stand. No clear differences were found in the mean volume of the 100 thickest trees in the stand between the larch and silver birch.
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Especially in forest vegetation studies, the light climate below the canopy is of great interest. In extensive forest inventories, direct measurement of the light conditions is too time-consuming. Often only the standard tree stand parameters are available. The present study was undertaken with the aim to develop methods for estimation of the light climate on the basis of readily measurable tree stand characteristics. The study material includes 40 sample plots representing different kinds of more or less mature forest stands of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.).
In each forest stand, a set of hemipherical photographs was taken and standard tree stand measurements were performed. A regression approach was applied in order to elaborate linear models for predicting the canopy coverage. The total basal area of the stand explained 63% of variance in the canopy coverage computed from hemipherical photographs. A coefficient representing the relative proportion of Norway spruce in the stand increased the explanatory power into 75%. When either the stand density (stems/unit area) or dominant age of the stand was included into the model, increment of the explanatory power into 80% was achieved. By incorporating both of the preceding predictors, an explanatory power of 85% was reached.
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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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Norway spruce (Picea abies (L.) H. Karst.) boards sawn from outer layers of logs were sampled from a sawmill in Northern Finland and another in Southern Finland. Test pieces 20 mm x 20 mm x 20 mm were selected according to maximum variation in growth ring width. Volumetric and longitudinal shrinkage from a soaked to a dry condition were measured. It was found that wood density correlated positively with the volumetric shrinkage but negatively with the longitudinal shrinkage. Dry density was a better predictor than basic density. With constant density and an increase in growth ring width, there was increased shrinkage, especially in samples from Northern Finland. Besides this, when density was kept constant, the shrinkage was higher in the spruce wood from Southern Finland than from Northern Finland.
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This article reviews experiments and practical experience of forest management by the selection system in Finland. In an experiment of 25-year duration the annual growth of uneven-aged Norway spruce (Picea abies (L.) H. Karst.) stands was only about 50% of the average annual yield of even-aged stands in normal rotation on the same site.
In Finland the selection system is applicable under exceptional conditions only, viz. In intensively managed park stands and, on the other hand, on very marginal sites, e.g. on peat bogs and mountains near the tree-line. Even normal silviculture, however, may include cuttings which somewhat resemble selection system, e.g. removal of standards or restoration of mismanaged forests.
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A total of 146 Norway spruce-dominated clear-cutting areas and 140 of the sample plots included in the 7th National Forest Inventory in Finland were examined during 1974–78. The micro-organisms causing decay in Norway spruce (Picea abies (L.) H. Karst.) sample trees were identified. The most common causal agent of butt-rot was Heterbasidion annosum (Fr.) Bref. Other fungi causing decay in the spruce trees were Armillaria mellea (Vahl.) Quél, Stereum sanguinolentum (Alb. & Schw. ex Fr.), Resinicum bicolor (Alb. & Schw. ex Fr.) Parm. and Climacocystis borealis (Fr.) Kotl. & Pouz. Species of Ascocoryne were very often present in the decay. The decay caused by H. annosum was considerably more extensive than cases of decay where the fungus was not present.
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The effect of growth rate on wood basic density in even-age Norway spruce (Picea abies (L.) H. Karst.) plantations was studied on the basis of samples collected from 53 stands; 30 trees were sampled in each stand. The prediction of basic density with the help of growth rate and some other tree characteristics could be improved if the social status of the tree was taken into account. Within a stand, the smaller trees had a lower density, while taller trees had a higher density than they should have had on the basis of growth rate alone.
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Basic density and absorbed energy in impact bending were measured for 500 Norway spruce (Picea abies (L.) H. Karst.) samples from Northern and Southern Finland. Statistical analysis showed that the relationship between impact strength and basic density was significant and regression analysis showed that it was linear.
Furthermore, with constant density, the impact strength was higher in Northern than in Southern Finland. This was due to growth ring width: i.e. when density was kept constant the impact strength increased with decreasing growth ring width. In addition, when the growth ring width was kept constant, the basic density of wood was higher in Southern Finland than in Northern Finland.
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The objective of the study was to compare different reforestation methods on ploughed areas in Finnish Lapland. Four species were compared: Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.), silver birch (Betula pendula Roth) and Siberian larch (Larix sibirica Ledeb.). The experiments were established in different parts of Lapland on different types of sites in 1970–72.
In Scots pine there was a difference of 15 percentage points in survival of seedlings between the best and worst methods of regeneration. Containerized seedlings and paper pot seedlings had the best survival rates. In Norway spruce the respective difference between sowing and planting was about 20 percentage points. In favour of planting. The survival rate can be increased by about 20 percentage points by selecting the right tree species. The average height varied from 25 cm (the sowed Norway spruce) to 179 cm (the planted silver birch) after 10 growing seasons. The birch was planted at the most fertile sites only. The longer time passed from the afforestation the clearer was the effect of the local growing conditions on the development of the seedlings. The elevation of the site was one factor seemed to influence the success of the seedlings.
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A population consisting of 450 Norway spruce (Picea abies (L.) H. Karst.) samples was gathered from northern and southern Finnish wood. The static bending strength was affected greatly by the density of the wood. However, keeping the density constant, the bending strength was higher in northern than in southern Finnish wood. The reason was the effect of the growth ring width.
The basic density was affected by the growth rate. Keeping the growth ring width constant, the basic density was over 5 kg/m3 lower in northern than in southern Finnish wood. This result supports the earlier findings on the effect of latitude.
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Ultrastructure of mesophyll of second-year green needles of Picea abies (L.) H. Karst. and Pinus sylvestris (L.) has been studied in several polluted areas in Finland since 1976 (Soikkeli and Tuovinen 1979, Soikkeli 1981a). Four different types of injuries have been found. The types differ with the origin of the material:
1) In needles collected from areas pollute by S-communds the types with reduced grana and/or the with lightening of plastogobuli with simultaneous accumulation of lipid-like material are observed.
2) In needles expose to fluorides (alone or in addition to other pollutants) the type with swollen and/or that with curled thylakoids are found. Both of the latter have also stretched envelopes. In each type of the injury three stages of cell disruption have been described: slight-medium, severe and very severe. On the slight-medium stage the injuries are usually found only in chloroplasts. On severe stage other organelles show injuries, too. In very severe injury all cell organelles are badly disorganized or they disappear completely. The most abundant injuries are usually in needles collected after their second winter. The severity of cell injury depends on the closeness of emission source or on the measured concentration of SO2.
The objective of the investigation was to determine the differences between timber grown on a peatland before and after draining, in respect of compressive strength parallel to the grain, static bending strength and density. In addition, the characteristics of boundary zone between the wood formed before, and after the draining with wider growth rings was studied. 41 Scots pine (Pinus sylvestris L.) and 22 Norway spruce (Picea abies (L.) H. Karst.) trees were studied.
The compressive strength of pine usually decreased from the butt end upwards, but no trend was observed in spruce wood. In coniferous trees, wide-ringed wood formed subsequent to draining was slightly lighter than the close-ringed wood produced prior the draining. The density of pine as well as spruce increases as the width of the growth rings decrease up to a certain limit. The strength of the different kinds of wood seems to decrease from the butt end upwards.
In both species, the compressive strength parallel to the grain and the bending strength are lowest in such wood that contains exclusively wide-ringed wood formed subsequent to draining. Also, compressive and bending strength increase with decreasing width of the growth rings. The longitudinal shrinkage of compression wood in spruce was several times that of normal wood, and the bending strength was lower than that of normal wood particularly in spruce. The compressive strength parallel to the grain in dry condition was, however, higher than in normal wood both in pine and spruce.
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The crown structure and stem growth of Norway spruce (Picea abies (L.) H. Karst.) undergrowth was studied in relation to the prevailing light conditions and potential photosynthesis. Shading decreased the stem height growth more than the length increment of laterals, producing a plate-shaped crown in deep shade. Needles responded to shading by adopting a horizontal inclination in deep shade. The needles were wide and thin respectively in shade. In the open the needle cross-section was almost square. Stem radial growth and height growth were both affected by shading exhibiting a linear response to the prevailing light conditions and the potential photosynthesis. Light conditions under dominating trees were closely correlated with the basal area of the dominating trees.
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Dependence of the growth increase given by fertilization on different stand characteristics is examined in this article. The aim was to determine whether the volume growth increase can be accurately determined beforehand when fertilization is carried out on mineral soil sites at a dosage of 120 kg N/ha. The material consisted mostly on of mature stands ready for cutting, a total of 22 Scots pine (Pinus sylvestris L.) and 20 Norway spruce (Picea abies (L.) H. Karst.) stands. Increase in basal area, height quality class and basal area of the stand were found to best explain the increment and its increase in the regression equations calculated for different types of fertilizer and the control level.
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The aim of the present study was to establish whether hormone treatments would promote flowering in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) grafts under Finnish conditions. Also, an attempt was made to test the efficiency of hormones as well as the variation in response among different clones. Six Scots pine and six Norway spruce clones were selected in each seed orchard based on their flowering intensity, and treated with growth hormones (GA, NAA) of different dosages by spraying. Flowering was observed one year after the treatments.
None of the treated or untreated spruce grafts flowered. However, poor flowering in the natural stands indicated that the environmental conditions during the previous years did not favour flowering. On the other hand, a distinct increase in flowering in Scots pine was observed as a result of spraying with hormone solutions. Treatments with gibberellin had a distinct promoting effect both on male and female flowering in the Scots pine grafts, although the responses varied between the different hormones or clones. The relative effect was generally stronger in male flowering.
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In this paper the connection between seed weight and amount and duration of growth are studied at the progeny level within stands or climatically uniform areas, and at the provenance level within larger geographic areas. The material consists of materials of several experiments in the nursery of Maisala in Southern Finland in 1971–76. The origins of the plant material used in the different experiments ranged from progenies of individual Scots pine (Pinus sylvestris L.) or Norway spruce (Picea abies (L.) H. Karst.) trees to provenance selections covering almost the whole natural range of these species.
The effect of seed weight on plant height is strongest immediately after germination and subsequently decreases steadily, when the genetic growth properties of the plants themselves become effective. The effect is usually visible at least until the end of the 1st growing season. This relationship varies considerably depending on the material studied. The connections between the duration and the amount of height growth also proved to differ according to the nature of genetic variation. In wide selection of provenances, which show clear genetic differentiation in annual growth rhythm. The variation in the duration of growth accounts for most of the differences in total height growth. At the individual and family level or between provenances of a limited area, there seems to be no clear connection between the duration and the amount of growth. It seems that the duration of the annual growing period is a genetic property, which is not affected by seed weight.
The total height alone in 1-year old test material grown in a greenhouse had hardly any value in the forecasting of growth capacity. The growth differences were caused mainly by the variation in seed size and growth rate differences during the growing period.
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Cutting propagation of forest trees has recently been done in Finland mainly by the Foundation for Forest Tree Breeding. The aim has been to develop methods which could be used in forest nurseries for large scale production of rooted cuttings. Methods are being developed for tree species which seem to offer possibilities for economically profitable vegetative propagation. The most important tree species has been Norway spruce (Picea abies (L.) RH. Karst.), and also larches (Larix sp.), lodgepole pine (Pinus contorta), birches (Betula sp.), alders (Alnus sp.) and hybrid aspen (Populus tremula x P. tremuloides) are propagated. The sensitive rooting phase takes place in plastic greenhouses which have ventilation on the roof top, mist irrigation equipment and separate heating systems for the air and the ground. Methods used for cutting propagation of Norway spruce, lodgepole pine, larch species and broadleaved trees are described.
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The study concerned with variations in the density of the wood of different provenances in provenance test series of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) RH. Karst.), established in 1931. Increment cores were collected from 10 sample trees from each sample block. The density of the pine wood was noticeably higher than that of spruce. The basic density was in average 450 kg/m3 for Scots pine, and the variation between different origins was 3–9%, while the average basic density of spruce was under 400 kg/m3 and the variation 3–10%. Statistically significant differences were found between the mean basic densities of different provenances in all sub-experiments for spruce, but only in one pine sub-experiment. However, these differences were not due to the altitude or latitude of the place of the origin. Volume growth seems to be the dominant component in the formation of dry matter yield.
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The productivity and several morphological features of Estonian Norway spruce (Picea abies L. Karst.) show significant geographical variation. This is no doubt because of differences in the climatic and soil conditions, which in spite of the small area of the country is quite large. In order to check the possible geographical variability of the gene pool, preliminary experiments were carried out in 1969, when seeds from 93 spruce stands originating from 14 forest enterprises were sowed in a nursery. After two years, the seedlings originating from south-eastern Estonia were the tallest. The seedlings from northern origins were smallest. However, it cannot be maintained that spruces from Southern Estonia are of better genotype than genotype from Northern Estonia since the genotypes are evaluated on the basis of ecological conditions under which the experiments are carried out. Another study suggests that an average shift of 7° to the east of the territory for spruces are suitable for cultivation in Estonia.
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Ecological investigations have shown that Norway spruce (Picea abies (L.) H. Karst.) reached Western Finland about 1,500–1,000 years B.C. and did not reach Åland islands before around the year 0. The species spread into Finland from the east and north-east, having survived the glaciation somewhere in the central parts of the Asian continent. Geographical variation has provided foresters with provenances of better growth and higher economic yield. In Finland, provenances, for instance, from Austria, Eastern Germany, Romania, Southern Poland and Slovakia have been planted in experiments, mostly in various parts of Southern Finland. According to the results of the experiments, it seems that for the more northern parts of Finland and Sweden the best material was to be obtained from north-east Europe.
The Scandinavian countries decided in 1975 to make a common assessment of all the provenance experiments with Norway spruce. The synthesis confirms the earlier view that provenances from the most north-eastern parts of Central Europe are of the greatest value for Finland.
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Material for this study was collected from 26 stands marked for clear cutting in Southern Finland. The volume of decayed Norway spruce (Picea abies (L.) H. Karst.) timber and pulpwood was determined by deducting the volumes of these assortments (as recorded on the measurement certificate) from the volume of the standing trees. To obtain the economic loss, the volume of decayed wood was multiplied by the difference in stumpage prices between spruce timber of pulpwood and pine pulpwood. In the 17 stands of Buyer A the loss in timber volume caused by decay was 5.84% and the loss in stumpage price 2.84 Fmk/m3 (means weighted by volume). The corresponding figures in the 9 stands of Buyer B were 10.87% and 5.50 Fmk/m3, respectively.
At the mean stumpage price level for the felling season 1977-78 the losses in the stands m.f.c. mentioned above were 2.87% per unit price in the stands of Buyer A and 5.75% in the stands of Buyer B.
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The potentials of forests in abatement of urban noise and air impurities are discussed based on literature and calculations. Excess attenuation of 6–7 dB seems to be possible in noise abatement applying Norway spruce (Picea abies (L.) H. Karst.) plantations. The potential in dust sedimentation is of 10,000–20,000 kg/ha/year and absorbtion to 7 kg/ha/yr. Forests seem also have considerable potential for control of climatic conditions in urban areas. Management of forests in urban environment is discussed.
This paper was presented in the ‘Man and the Biosphere’ programme Project 2 seminar held on August 24–25 1978 in Hyytiälä research station of University of Helsinki.
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Ashed tree samples from sound and decayed Norway spruce (Picea abies (L.) H. Karst.) were studied by means of fast neutron activation analysis, and for comparison, also by X-ray fluorescence analysis. In fast neutron activation analysis, the following elements were detected: (Na), Mg, Al, Si, K, Ca, Mn, Rb, Sr and Ba, and according to the results of the X-ray fluorescence method the elements present in the wood samples were: K, Ca, Mn, Rb, Sr and Ba. A general diminishing was revealed by both methods in most elemental concentrations studied, with exception of K and Rb, when going from a sound tree to a decayed one. The use of the ratio of the amounts of potassium to calcium as an indication of the degree of decay is therefore proposed.
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The aim of the study was to determine which kinds of insects had infected the Norway spruce (Picea abies (L.) H. Karst.) in different stands killed by flooding caused by beavers (Castor canadensis Kuhl), and if there was any danger that they would subsequently cause damage in the surrounding forests. The effect of tree diameter and certain stand characteristics on the fauna of dead trees are discussed. The occurrence of different insect combinations and qualifications for their coexistence were studied.
Pityogenes chalcographus L., Trypodendron lineatum O., Hylurgops palliatus Gyll. and Dryocetes autographus Ratz. occurred most abundantly. 20 phloem or wood boring species were observed in 5 regular succession types. Secondary species occurred in a virgin stand while Ips typographus L. was found at the edge of a felling area. Owing to the flooding, species preferring moist conditions were abundant. In this case damages had not spread to the surrounding forests which, however, might be possible under certain conditions.
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This study, comprising three experiments, aims to determine the effect of the geographical origin of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) seeds, and the duration of the time lag between the moisture treatment and subsequent irradiation on the gamma-irradiation sensitivity of seeds.
The studies showed that the greater the irradiation dose seeds were subjected to the slower the rate of germination. In general, small radiation doses (250–1,000 rad) had a stimulating effect and the final germination percentage (36–40 days) increased. However, when the level was further increased, the germination percentage decreased. Air-dry and moistened seeds withstood irradiation better than others. In a study with moistened seeds from different geographical sources, pine and spruce seeds from Northern Finland were less able to withstand irradiation than those originating from the south.
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The aim of the paper was to study the amount and distribution of rainfall in a virgin Norway spruce (Picea abies (L.) H. Karst.) stand. Special attention has been paid to the dependence of throughfall on the characteristics of the precipitation falling on an open area and the stand.
The throughfall was 62% of the precipitation in the open. The best independent variable as regards the throughfall was the amount of precipitation falling in the open. The heaviness of precipitation in the open gave no meaningful correlation. Horizontal layout of the stand was found to have some effect on the throughfall. The throughfall was also influenced by the tree species composition of the stand. Only 52% of the total variance of the amount of water caught by the rain gauges could be predicted with the characteristics of the precipitation in the open and the stand.
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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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Photosynthesis and dark respiration in five families of autochtonous Norway spruce (Picea abies (L.) H. Karst.) and in seedlings from twenty Finnish stands of Scots pine (Pinus sylvestris L.) were investigated in constant environmental conditions. Values of CO2 exchange were compared with the height growth and weight of seedlings in Norway spruce and with the weight alone in Scots pine. No statistically significant differences were found in CO2 exchange among progenies or stands. Photosynthetic efficiency and photosynthetic capacity showed a positive correlation both in spruce and in pine. Growth and net photosynthetic capacity were linearly and positively correlated in pine. Spruce and a higher light compensation point than pine. The use of an open IRGA system with several simultaneous measurements and the trap-type cuvette construction in genetic work are discussed.
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The paper deals with the relationships between macronutrients, ground vegetation and tree crop on a drained peatland area in Central Finland. The former herb-rich spruce swamp was drained in 1930s. The Norway spruce (Picea abies (L.) H. Karst.) stand was established by planting under a nurse crop of birch, which was removed later.
There was a negative correlation between the thickness of the peat layer and the volume and mean height of the growing stock. This was found to depend on the negative correlation prevailing between the potassium content of the topmost peat layer and the thickness of the peat cover. The deficiency of potassium is clearly discernible as deficiency symptoms in the needles, the intensity of which showed a strong correlation with the stand characteristics studied. Among the nutrient characteristics of the topmost peat layer, total potassium and the N/K and P/K ratios showed the closest correlation with the stand characteristics. The communities into which the ground vegetation was divided differed from each other with regard to the calcium content of the peat substrate.
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The study deals with the variation in the proportion of heartwood in Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) both within and between stems as examined on the basis of literature. Special attention is paid to an application, in which on the basis of the diameter of pulpwood bolts, efforts are made to predict the proportion of heartwood in the total volume of bolts. It is shown that the method, even when based on homogenous material of 564 Norway spruce and Scots pine bolts, easily leads to wrong conclusions concerning the proportion of heartwood.
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The study was an attempt to assess, from a theoretical viewpoint and with the techniques of measurement in mind, the usability respiration and cumulative respiration in the observation of the progress of seed germination in Norway spruce (Picea abies (L.) H. Karst.), as well as the influence of air temperature substrate moisture and the stage of physiological development of seeds on respiration. Furthermore, the reserve nutrient consumption and the possible uptake of mineral nutrients were kept under observation during the 9–11 days after seeding.
The results showed that the stage of physiological development of the seeds can be rather well described by the means of cumulative CO2 release. There was a strong interaction in the CO2 release between the moisture of the substrate and the air temperature. It seems to be to great extent due to differences in the rate of development in the early phases of germination. The CO2 release from seeds showed a close correlation with percentage germinated seeds.
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A growing stand of Norway spruce (Picea abies (L.) H. Karst.) marked for cutting was investigated in the winter of 1971–72 in Helsinki in Southern Finland in order to determine the economic loss caused by decay. Taking a sample from growing spruce trees with increment borer is not a reliable method of determining the frequency of decay. The decayed stems were twice measured for assortment cutting into lengths; the first time disregarding the decay and the second time doing the actual assortment cutting according to the grade of timber. The direct economic loss caused by decay was 13% of the price for standing timber. The indirect loss may be as great as the direct loss.
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The material comprised 12 Norway spruces (Picea abies (L.) H. Karst.) from Central Finland, with 2,118 branches. The exact location of the branches on the stems, their diameter at the thick end, their length, and the green weight of all the branches was measured on two-metre lengths of the stem.
According to the results, the diameter of a branch can be estimated very accurately from its length. The variation of branch diameter along the stem was also very regular, although there were considerable differences from one tree to another. The greatest work requirement for trimming was in the middle and upper parts of the green crown. Branch variables per tree, such as the number and cross-section area o the branches, could be satisfactorily estimated from the volume or breast-height diameter of the stem.
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The study was carried out in a Norway spruce (Picea abies (L.) H. Karst.) stand in Southern Finland which was to be clear-cut due to decay. The species composition and incidence of decay fungi were investigated from the cut surfaces of the stumps. In addition, the colour and size of the decayed spot was observed.
About 28% of the total number of trees were decayed. Fomes annosus (Heterobasidion annosum) was the most common decay fungus. It was identified from 75% of the decayed trees, and was the sole agent in 43% of these trees. Armillaria mellea was the second commonest decay fungus. It decayed trees mostly in combination with Fomes annosus. The most common colours of the decay produced by F. annosus were reddish or yellowish brown. The decay caused by A. mellea was blackish brown. The causative agent cannot be reliably identified on the basis of the colour of the decayed part.
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The paper describes the results of a fertilization experiment, in which transplants of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) were fertilized with various doses of fine-ground copper rock phosphate (33% P2O5, 4% Cu) placed direct in the planting hole. The experiment was made in northeast Finland on a clear-cut, burnt-over and furrowed moraine heath. The fertilization increased especially the survival and condition of the Scots pines and increased to some extent also the height growth of the plants. The spruce survived better than the pines.
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This article is an abstract from a lecture given in Helsinki on 2.12.1970. Physiological differences in different parts of developing primordia of micro- and macrostrobiles are manifested in the ultrastructure of the cell tissues. In electron microscopy, the study off metabolic activities can be combined with the anatomical examination of the flower primordia.
The generative cells of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) develop under the strong metabolic activity of surrounding layers of cells. Simultaneously the activity and development of the organelles in generative cells becomes hindered, and these inhibitions will exist until the fertilization. It can be concluded that the higher the gradient of sexualization of the cells in different parts of flower primordia, the weaker the metabolic activity in these cells.
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About 4,000 seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) were planted in 1965 both on a clear-cut and sheltered area in Central Finland. In the autumn of 1966 needle colour was determined by using Muncell Color Charts which allowed a quantitative measurement of three colour dimensions (hue, value, and chroma). Terminal shoot growth was recorded for two years after colour measurements. In both species, fertilization (NPK in the spring of the year of colour measurement) as well as other site factors caused differences in all three dimensions of needle colour. A regression of shoot growth on needle colour was found in both species. In most cases colour value (darkness) and, in spruce, also chroma, predicted the subsequent growth almost as well as did these two-colour variables together.
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The material of 78 damaged Norway spruce (Picea abies (L.) H. Karst.) trees was gathered in Southern Finland in order to clarify the advance of decay. The harvesting which had caused the scars had been carried out 12 years earlier and at the moment of the investigation the growing stand was 110 years old. It was noticed that the variables used could explain only a few per cent of the variation of the advance of decay. It was concluded that the only important thing in practice is whether the injuries are in roots or in stems.
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Experiments were carried out to find out the effect of fertilizer application on germination, seedling emmergnece and initial development in conifer plantations established on peat by sowing, with a special reference to Scots pine (Pinus sylvestris L.). The experiments were carried out in 1968–70 in laboratory, in greenhouse and in the field.
In the greenhouse experiments with Y fertilizer for peat soils (14% N, 18% P2O5, 10% K2O) it was shown that germination and seedling emergence decreased markedly with increased fertilizer application. Mortality among seedlings that had emerged was the higher the larger quantities of fertilizer had been applied. The effect of fertilization was the greater, the drier the substrate. Fine ground rock phosphate (33% P2O5) promoted seedling emergence on a dry substrate but not on a wet one.
The field experiments carried out in Central Finland included dry and wet sites. Y fertilizer, Oulu Saltpeter (25% N), fine-ground rock phosphate and potassium salt (50% K2O) were used. According to the results, easily soluble fertilizers decreased seedling emergence. On wet sites the effect of Y fertilizer was weaker than on drier sites. Fine-ground rock phosphate slightly increased the number of seedlings emerging. Height growth was increased during the first three growing seasons only by those fertilizers containing phosphorus.
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In the eastern parts of South-Finland the growing season of 1967 was highly favourable, which resulted in good height growth during the following year. During the summer 1968, temperature conditions were unfavourable, while the middle of summer was cold and the later part of the growing season unusually hot. The following winter had exceptionally cold spells from January to March, which caused Norway spruce (Picea abies (L.) H. Karst.) abundant winter frost damages such as dead shoots and buds, and destroyed needles.
These damages occurred particularly in stands with height of 0.5–3 m, and the occurrence of damages seemed to concentrate to the parts of saplings that had been immediately above the snow cover. Detailed observations on spruce plantations growing under a dense nurse stand of alder (Alnus sp.) indicated that explicitly the top shoots suffered from damages and not so much the laterals. When the needles of the leader suffered from minor damages, the shoot continued to grow normally. Still, sometimes a branch took over and became a new leader. If only the leader bud was killed, further stem development became dependent on one of the topmost lateral buds. When the upper part of the leaded died, one of the lateral shoots at its base usually became the new leader.
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The study was carried out in order to establish the possible influence of damage caused to the needles of Picea abies (L.) H. Karst. by the spruce spider mite, Oligonychus ununguis (Jacobi), and the growth of the damaged seedlings. The study was carried out in 1968–1970 by comparing growth of seedlings infected with spruce spider mite with that of seedlings where mites had been killed with acaricide (Eradex®). In the seedlings that had not been treated with acaricide, the number of wintering eggs were 60, 20 and 5 per shoot in the various years of the study. When the experiment was laid out, before planting and acaricide treatment, the seedlings were four years old, all seadlings were heavily infected, the number of wintering eggs being 100 per shoot. The growth of infected seedlings was 3, 20 and 15% smaller than that obtained for the seedlings which had been treated with acaricide.
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Seed development was microscopically studied after controlled pollinations. In all the interspecific crosses incompatibility occured. In the following crosses the growth of all the pollen tubes stopped before they had penetrated through the nuclear cap: Picea abies (L.) Karst. x mariana, abies x jezoensis (and the reciprocal), abies x omorika (and the reciprocal), mariana x asperata, mariana x jezoensis and Picea abies x Pinus sylvestris L.
Some of the eggs were fertilized in the crosses Picea abies x glauca (and the reciprocal) abies x asperata, abies x koyamai, abies x obovata, mariana x omorika and jezoensis x omorika. Embryo degeneration was observed in all these crosses. All the embryos died in the crosses abies x glauca (and the reciprocal) as well as jezoensis x omorika. Adequate amounts of full seed for germination test was obtained from the crosses abies x asperata, abies x koyamai and abies x obovata. In all these crosses there were seeds which were able to germinate and the hybrids are now one growth season old.
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This paper presents the results of a contest performed on behalf of the Finnish bank Kansallis-Osake-Pankki and the Central Forestry Board Tapio on growing trees on peatlands. Over 5,000 sample plots were established on drained peatlands in various parts of Finland. The aim was to achieve a best possible growth of seedling stands on peatland. The factors influencing the growth of 85 best Scots pine (Pinus sylvestris L.) and 60 best Norway spruce (Picea abies (L.) H.Karst.) sample plots were studied.
The height growth of the seedling stands decreased towards the north. Fertilization seemed not to decrease the regional differences; rather on the contrary. On the other hand, fertilization increased height growth, but evidently so that the increase obtained was greater in the southern than in the northern parts of the country. Light fertilization (50 kg/ha of K2O and 60 kg/ha of O2P5) caused a clear increase in height growth while heavy fertilization (100 g/ha of K2O and 120 kg/ha of O2P5), had same effect but to much greater extent than the former. Spruce seedling stands in particular benefitted of the heavy fertilization.
Fertilization did not eliminate the original differences in the quality of the sites in question, but these could still be seen in the height growth after fertilization. The effect of drain spacing on the height growth was not very clear. In dense seedling stands (800 seedlings/ha) the height growth of the dominant seedlings was greater than that obtained in stands of lower density. Hold-overs caused a decrease in the growth of the seedling stands.
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The aim of the study was to establish how the cold storage of cones of Norway spruce (Picea abies (L.) H. Karst.) affects the viability of the seeds and the percentage ratio in 7 days. A parallel study was made of the longevity of seed in barn-stored cones subject to weather fluctuations and the longevity of seed extracted immediately and stored in the conventional way in an air-tight container. The cones were collected near Kuopio in Central Finland and near Tampere.
The viability and germination rate of the control sample was constant throughout the storage period. This storage method proved the best. The viability of seeds kept in cones declined in cold storage after 3 ½ months. The cones collected in Tampere were damaged by Laspeyresia strobilella, which affected the viability of the seeds.
The viability of seeds stored in cones in a barn had not weakened by the end of May, however, they deteriorated during the summer, as did the seeds stored in cones in the cold storage. Viability of the seeds was still 94% in October. The germination rate was constant in each lot up to the end of May, after which it decreased to 81.7–86.1% in October.
The results show that healthy spruce cones can be stored in paper sacks in a single layer in cold storage and in an ordinary barn for several months without it affecting the viability of the seeds.
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The aim of this study was to establish the need of treatment of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) seeds to be sown in greenhouse. 3 x 100 seeds of each treatment (soaking in water, treatment with Pb3O4, treatment with tiram-containing coating substance) were sown in a glasshouse on a fertilized garden peat, and covered with peat layer of 6 mm thickness. The development of seedlings was followed for 100 days before the final measurement.
Soaking the seeds with water made germination somewhat faster. In spruce the germination percentage increased, but the opposite was observed in pine. No difference could be observed between the results from soaking with acid water from peat soil and lake water. Drying the soaked seeds for a week before sowing had no harmful influence on the germination or the early development of the seedlings. Treatment with Pb3O4 did not affect the germination speed or the seedling percentage of pine or spruce, but increased the germination percentage of spruce. Coating decreased germination and seedling percentages in pine. However, the differences between the treatments were so small that their practical significance is negligible.
Germination of both the species initiated on an average in 8 days, and 16 days after sowing 80% of the seeds had germinated. Seedling mortality was about 10% of the total number of seedlings, the most common reason being damping-off.
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In Finland the mite Nalepella is found in Norway spruce (Picea abies (L.) H. Karst.) in forests practically in every tree, and even in the nurseries. The paper reports on the occurrence of Nalepella Haarlovi var. picea-abietis Löyttyniemi in Finland in tree nurseries in Finland. The study is based on a large material, collected in connection with an investigation into spruce spider mites.
Nalepella lives vagrantly on the needles. Due to the sucking of the mites, the needles turn yellow, become dry an die. Single patches from sucking cannot be seen by the naked eye. They occur on all sides of the needles. The worst damage to spruce seedlings in nurseries is caused to the needles located in the top of the seedling. Sometimes the terminal bud dryes and the whole terminal shoot can die. However, the whole seedlings seldom die in consequence of the Nalepella mite alone. Subsequent damage to the injured needles is often caused by fungus Cladosporium herbarum.
The study shows that the mite causes economically significant damages only in the nurseries. In forests no such damages were observed in seedlings or in older trees. In 1965–68, significant damages occurred in 16 nurseries in Finland. About 600,000 four-year-old seedlings were destroyed in 1967. The damages were economically important only in the 4-year-old seedlings.
According to the study, seedlings damaged by Nalepella can be used for planting as they recover rather well after planting in the forest. Moreover, the damages end after planting, and density of the mite population decreases during the first summer.
The mite overwinters as egg on needles. The eggs hatch in Southern Finland in the end of April and in the beginning of May.
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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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This lecture discusses the problem of the annual variation in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.), and its significance. A newly constructed instrument for field measurements of diameter growth is described, also the latest of the Royal College of Forestry’s series of machines for annual ring measurement. The method of constructing an annual ring index is also mentioned.
Examination of material from undisturbed stands in Northern Sweden has shown that the annual ring index series for pine are characterised by a relatively marked autocorrelation, which increases with latitude, implying that the annual ring index for a given calendar year is positively correlated with that for the year immediately preceding it. However, this seems not to be so in spruce, in which the annual ring index series is marked by the effect of the changes in cone production from the year to year. The annual ring index for spruce may be expressed in the form of climatic functions, according to which the index can be approximately calculated or known values of the meteorological variables contained in the function, in association with numerical expressions for the cone production. By means of a number of examples illustrating annual ring series from thinned stands. It is shown finally how the response to thinning can be presented in a more essential form from the variation in the annual rings, and how climatically corrected increment can be determined.
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This study elucidates the composition of the microfungal populations of the humus layer of tree forest types – Vaccinium type with Scots pine (Pinus sylvestris L.), Myrtillus type with Norway spruce (Picea abies (L.) H. Karst.) and Oxalis-Myrtillus type with birch (Betula sp.). The results indicate that the microfungi encountered in these sites bear close resemblances. The number of species increased but little towards the more fertile sites from VT to OMT. The main difference was limited to the quantitative relationships between the species.
The microfungal density in the humus layer was greatest in VT, and only slightly less in MT and OMT, in this order. In all the sampling areas, occurrence of the microfungi reached a maximum in the middle of summer, at a time when the maximum temperatures were registered in the humus. The quantitative abundance during the early autumn bears a relation to the yield of litter.
The microfungi most commonly encountered in all sampling areas were those of rapid growth, Mucor, Morierella and Penicillium species, along with Trichoderma, a little slower in growth, and actively decomposing cellulose. Mucor fungi, favouring moisture, were most abundant in the early summer and in the autumn. The Mortierella and Penicillium species, which survive dryness, were most abundant in the middle of the summer. The former is twice as common in MT and OMT than in VT, and the latter twice as common in VT as in OMT.
Scopulariopsis and Verticillium species were found regularly in MT and OMT. One Acremonium species was found almost exclusively in VT, and some Aspergillus and Mycogene in OMT alone. Sterilia mycelia was relatively abundant in MT and OMT in particular. Different kinds of yeast fungi were encountered generally in MT and OMT.
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The present study deals with the occurrence of the rust, Pucciniastrum padi (Kunze & Schm.) Diet., in the shoots and cones of Norway spruce (Picea abies (L.) H. Karst.) in the forest area of the training and experimental farm of Helsinki University at Viikki (60’10’ N; 25’ E). The most important task was to clarify the correlation between the occurrences of the disease in spruce and the abundance of the alternative host of the disease, bird-sherry (Prunus padus L.).
Infected shoots were encountered in a 17-year-old planted seedling stand of spruce. In this stand 8.4% of the seedlings were infected. The density of bird-cherry trees was in the stand higher than in the surrounding areas. The number of infected shoots was the greatest in those places where the density of bird-cherries was highest and already at a distance of some ten metres form the bird-cherry stands the degree of infection decreased considerably. The portion of infected cones in the whole material of this study was 19.5%.
The dependence of the frequency of disease on the abundance of bird-cherries at different distances from the spruce stand was studied by means of regression analysis. For this reason, the percentage infected cones were determined by sample plots and the abundance of bird-cherry trees from six zones (0–50, 50–100, 100–150, 150–200, 200–300, and 300–500 m) around each sample plot. The results showed that the dependence between the degree of infection of cones and the abundance of bird-cherry in the surroundings only reached the closest zone. There were also infected cones at greater distance, for instance, 200–300 m from the bird-cherries about 10% of the cones could be infected. Both the infected cones and shoots were longer than the healthy ones.
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Stand precipitation and stemflow studies became necessary in connection with hydrologic studies, for instance, to explain the deviations resulting from rains in the ratios between the water content of peat and the groundwater level, throughfall during rains of variable heaviness, and effect of stand treatment on soil moisture level. In this project the distribution of rainfall in stands differing in species composition and density was studied in Central Finland in 1963–1965 in fifteen stand precipitation sample plots. In addition, rain gauges were situated under individual Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst.) and birch (Betula sp.) trees.
The average precipitation in the open was 4.8 mm, the corresponding precipitation in the stand was 77% for birch, 71% for pine and 62% for spruce. Measurements of stemflow from individual sample trees showed that less than ¼ mm (about 1.5%) during a 15 mm rain in a pine stand. In the spruce stands stemflow is negligible. A part of the sample plots was in drained peatlands with a dense vegetation of small shrubs. The shrub layer retention was about 10% even during heavy rain. In a small forest clearing, the bordering effect of the forest was seen up to the distance of 5 metres from the edge of the forest. During the period of study, on an average 3% more precipitation was recorded in the clearing than in the open, the difference being probably due to the stronger wind effect in the open.
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The aim of this project was to investigate the cellulose decomposition rate in the soil on the ecological conditions created by different tree species, particularly birch (Betula sp.) and Norway spruce (Picea abies (L.) H. Karst.). Therefore, comparable sample plots were established in adjoining birch and spruce stands. Data on the stands, the vegetation, and the soil in the sample plots were collected. The experiment was carried out in the Ruotsinkylä Experimental Forest near Helsinki in Southern Finland.
Five pieces (3x5x0.15 cm) of cellulose (bleached sulphite pulp) were dried, weighed, and fastened in a row into a nylon bag. The bags were placed into the soil at a slant so that the upmost piece of cellulose was in the depth of 0–1.5 cm and the bottom one 6–7.5 cm. The weight losses of the pieces were measured after periods ranging from 6 to 12 months.
The results show that even within the same forest type, decomposition is much more rapid in birch stands than in spruce stands. In all the stands the decomposition rate decreased rapidly with increasing depth. The difference between birch and spruce stand, as well as the decrease with increasing depth, was probably mainly due to different thermal conditions.
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The many unsolved questions concerning fertilization makes it difficult to forecast accurately its biological and economic consequences. Some of the problems are discussed in this paper. The most common types of forests in Sweden, Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) stands on well-drained mineral soil, respond strongly to nitrogenous fertilizers, but the effect of phosphate, potash or lime is small or nil, at least within 5–10 years after application. The response of nitrogen lasts 4–5 years in pine and somewhat more in spruce.
Drained peatlands usually respond to mineral fertilization, but the improvement brought about by a PK application depends, inter alia, on the nitrogen content of the peat. Peatlands with a peat low in nitrogen need NPK fertilization. For deep peatlands, a moderate or high nitrogen content, a single PK application improves growth conditions for a very long time. Experience of fertilizing shallow peatlands and poorly-drained mineral soil is very limited, but it seems easy to get a growth response either with nitrogen alone or with NPK.
The results of fertilization at the time of planting have not, as a rule, been very good in Sweden. An exception is the afforestation of abandoned fields on drained deep peat, where PK fertilizer around the plant seems to be essential for both survival and growth.
Since 1954 studies have been carried out by the Department of Plant Pathology of Agricultural Research Centre on occurrence of low-temperature parasitic fungi in nurseries in Finland. This paper reports analysis of the damage caused by the fungus to Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) seedlings.
In Southern and southwestern Finland, scarcely any damage caused by low-temperature parasitic fungi to coniferous seedlings was found. On the other hand, in Central, Eastern and Northern Finland, considerable injuries were present in the seedlings. The extent of damage varies between different localities and in a same location from year to year. The extent of damage is mostly dependent on snow cover which is heaviest in Central and Northern Finland. Damages are largest in wooded areas and in places where snow accumulates abundantly and remains until late in the spring.
The principal cause of winter damage to spruce seedlings is Hepotricia nigra (Hartig) which causes black snow mould. Depending on the amount of infestation, the damage can be limited to scattered groups or consist of large areas of dead seedlings. The fungus is unable to infect the plants during warm months of the growing season. The most damaging parasitic fungus in Scots pine is Phacidium infestans (Karst.) causing snow blight. The infestation varies from reddish-brown patches of infected seedlings to large areas of infected plants. Also, Botrytis cinerea has been determined from one- and two-year plants of pine and spruce.
In trials of chemical control by PCNB (pentachloronitrobenzene) gave nearly complete control of low-temperature parasitic fungi in one-year spruce seedlings. In addition, a compound of zineb (Dithane Z-78) gave similar results. Chemical control of the fungi is now common in the nurseries.
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Prescribed burning has reported to avail forest regeneration, for instance, by releasing nutrients for the use of seedlings, changing the pH of the soil and decreasing competition of ground vegetation. The aim of the study was to find out if the effects could be verified. Sample plots were measured in the experimental area of Tuomarniemi, in Central Finland, both in previously burned and untreated seedling stands and young forests. The main species in the sample plots was Scots pine (Pinus sylvestris L.).
According to the results, prescribed burning prepares the soil for regeneration. Germination percentage of the seeds is higher on the burned soil. All the species, Scots pine, Norway spruce (Picea abies (L.) Karst.) and birch species (Betula sp.) grow faster. Prescribed burning increases the amount of birch seedlings by improving its regeneration compared to unburned sites. The seed trees survive burning better if they are tall and have short crown, and have thick bark. In general, prescribed burning improves regeneration in seed tree stands.
The article includes a summary in German.
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.
The article includes an abstract in German.
Silva Fennica issue 52 includes presentations held in professional development courses, arranged for foresters working in public administration in 1938. The presentations focus on practical issues in forest management and administration, especially in regional level. The education was arranged by Forest Service.
This presentation describes different types of fellings in Norway spruce (Picea abies (L.) H. Karst.) forests in different forest site types. The use of thinning from below and above, clear cutting of Norway spruce stands, and thinning of mixed forests with birch (Betula sp.) are discussed.
Silva Fennica issue 52 includes presentations held in professional development courses, arranged for foresters working in public administration in 1938. The presentations focus on practical issues in forest management and administration, especially in regional level. The education was arranged by Forest Service.
This presentation describes the state of forests in Northern Finland, and suggests that fellings are targeted at the oldest forests until the over-presented over-aged forest are harvested. The preferred regeneration method is natural regeneration in most forest types.
Silva Fennica issue 52 includes presentations held in professional development courses, arranged for foresters working in public administration in 1938. The presentations focus on practical issues in forest management and administration, especially in regional level. The education was arranged by Forest Service.
This presentation describes a study of forest management practices suitable for in Hylocomnium-Myrtillus site type forests, typical for Northern Finland. A special problem for the forest site type is poor regeneration due weak seed production of Norway spruce (Picea abies L. Karst.) and thick moss layer.
Finnish tree species have adapted differently to heavy snow loads that occur especially in fell areas in Kuusamo and Salla as well as Maanselkä area in Sotkamo and Rautavaara in Northern Finland. Norway spruce (Picea abies Karst. L) is adapted better than Scots pine (Pinus sylvestris L.). The aim of this study was to investigate how crown and stem form of Norway spruce in the snow damage area of Maanselkä area differ from other areas in the same region.
Relatively broad crown at the base of the stem, quickly tapering crown and narrow and even upper crown were typical for trees growing in the snow damaged areas. The higher the altitude is, the stronger tapering the crown is. The tapering begins usually in a height of 4-5 meters. Even the stem diameter begins to taper strongly at this height. In the areas where heavy snow does not cause snow damage, top of crown is broader. Also, in the snow damage areas the damaged trees seem to have broader crown shape than the trees with little damages.
Height of the trees decreases in the snow damage areas compared to forests in lower altitudes, which can be caused both by wind and snow load.
The article includes a German summary.
Silva Fennica issue 42 includes presentations held in professional development courses, arranged for foresters working in public administration in 1936. The presentations focus on practical issues in forest management and administration, especially in regional level. The education was arranged by Forest Service
This presentation describes the principles of reneneration felling in Norway spruce (Picea abies (L.) H. Karst) stands.
Broadcast sowing on snow was relatively new method in the beginning of the 20th century in Finland, and the experiences of regeneration were diverse. The aim of the survey was to study the success rate of regeneration in the oldest and largest areas regenerated with this sowing method in Tuomarniemi district. Scots pine (Pinus sylvestris L.) was the most common tree species, but also Norway spruce (Picea abies (L.) H. Karst.) and European larch (Larix decidua Mill.) were used in broadcast sowing on snow.
According to the study, the success of broadcast sowing on snow was as good as patch sowing and sowing in furrows in the sites typical for Tuomarniemi. The regeneration areas were often drained peatlands or paludified lands. When sowing is done using Norway spruce seeds, site preparation either by broadcast burning or scalping with hoe is recommended. Mixed sowing with pine and spruce seldom succeeded due to the differences in site requirements of the species and growth of seedlings. Sowing of Scots pine succeeded well on the drained peatlands. Sowing should be done some years after draining to let the peat dry and sink. Site preparation is needed in sites growing Polytrichum-moss. Broadcast burned areas larger than 10 hectares seemed to regenerate poorer than sites in average, possibly due to dryness of the sites. Trials with European larch were successful, and the growth of the seedlings acceptable despite the sites being relatively poor for the species.
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A Committee was appointed in 1931 to prepare a program to improve the trade of small timber and to develop Finnish fuels and their production. The low demand for small timber is caused by the reduced export of Egyptian balks, and decreased demand of fuel wood that have been replaced by the imported fuels, like coal. At the same time, the supply of small timber has grown significantly due to increased thinnings, and better transport facilities that have made timber more accessible. Also, decreasing demand of large timber has increased the supply of small timber. The demand of small timber concentrates on Norway spruce (Picea abies (L.) H. Karst.). The sales of small timber are crucial from the silvicultural point of view. Selection felling of large timber in the past has reduced the supply of logs and led to surplus of small timber.
The article discusses the uses of small timber and potential new fields, such as wood sugar as fodder or refining wood as fuel. The use of timber should be promoted especially in the domestic industry. The Committee suggests funding for an additional forestry teaching post in the University of Technology, for forest technology and forest economics research in the Forest Research Institute, for research in wood technics, and for follow-up of forest sugar and wood gas fields.
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A Commission was appointed to examine the significance of pulpwood exports from the political-economic and social point of view. A survey was made of the development of woodworking industry in Finland. The article includes a detailed review on paper industry in Finland and abroad, pulpwood resources in Finland and outlook of the industry. The export of pulpwood was significant in 1925-1927, the most important country being Germany. The commission notes that It would be more profitable to refine the wood into more expensive products. It does, however, not see it necessary to restrict export of pulpwood. If restrictions are considered necessary, prohibition of export is a better way than export duties.
The best way to promote domestic paper industry is to increase the supply of Norway spruce (Picea abies (L.) H. Karst.). Measures are suggested to increase the productivity of the forests through forest improvement. The annual increment of spruce is calculated to cover the consumption in near future, provided the export of pulpwood does not amount to 600,000 m3, and the local demand of pulpwood does not exceed 7.8 million m3 annually. The Commission proposes that state ownership of forests is increased, forest management is intensified, and restrictions of forest industry to acquire forest land are removed.
It suggests also reliefs in taxation and import duties on fields related to transport, and equipment and raw materials needed by the paper industry.
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Norway spruce (Picea abies (L.) H. Karst.) is rarely the dominant species on dry mineral soil sites in Northern Finland. These sites are, in general, too poor and dry for spruce, and suit better for Scots pine (Pinus sylvestris L.). According to the study, the natural regeneration of spruce is in Northern Finland poor. In the sample plots, cones could be found in 35% of spruce trees in the stands in natural state and 46% in the harvested stands. Compared to the spruce areas in Northern Finland, or fresh mineral soil sites in Southern Finland, cone and seed production of Norway spruce was in dry mineral soil sites very low due to scarcity of seed trees and their low cone number. There were few spruce seedlings in the sample plots, but according to the observations, spruce is able to regenerate on lichen and heath covered sites. The seedling growth was, however, poor on dry sites. Spruce seedlings were often found near fallen trees and stumps. The growing trees prevent growth of seedlings of all species. Norway spruce seems, however, to be able to spread also to the poor sites. The success depends on the vegetation and dryness of the site. For instance, spruce can spread to dry mineral soil sites from seed trees of nearby peatlands.
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The present study proposes to calculate the economic sequence of two of Finland’s three main tree species, Norway spruce (Picea abies (L.) H. Karst.) and silver birch (Betula pendula Roth) when planted on Oxalias-Myrtillus type sites where both species are equally suitable, on biological grounds. In addition, the accuracy and applicability of the present Finnish yield tables to an economic comparison is tested. Benefit/cost ratio was selected as criterion of profitableness. All future net incomes and costs were discounted into the planting time and added together. The ratio between the discounted net revenues and the discounted investment costs (later called profit ratio) was the criterion. There is no reliable method to forecast the future wood prices, therefore two price ratios, birch veneer timber to spruce pulpwood and birch cordwood to spruce pulpwood, were chosen as free variables. The economic sequence of the tree species was determined as the function of these variables.
The main conclusions are, first, that under the present price ratios spruce appears to be the better choice for the forest owner, and the most promising policy for changing the situation seems to decrease the production costs of plants in birch nurseries. Second, the present Finnish yield tables are not consistent or accurate enough to enable any sufficiently reliable economic comparisons of tree species in artificial regeneration. The possible error of difference between two rather uncertain estimates is big. More work is needed to construct a uniform system of yield tables covering all main tree species, all site types, all macro climate conditions and all types of regeneration.
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In this study an attempt was made to use manometric Warburg technique in studying the growing season variations in the respiration rates of the roots of 1–3-year-old seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.). The respiration rates in both short-roots and long-roots have also been investigated.
According to the results, respiration intensity was the greatest in Scots pine and Norway spruce short-roots but also considerable in the long-root tips at the points of elongation. When the oxygen uptake rate per weight unit in the pine short-roots is given value of 100, the rate in the long-root tips is 61 and in the basal area 36. The corresponding values for spruce are 100, 69 and 43. The relative carbon dioxide release rates are different for the basal parts of the long-roots: pine 53 and spruce 57, when the CO2 release from the short-roots is 100. The CO2 release rate in the basal parts of the long-roots is relatively greater than the oxygen uptake. The respiration rate of the root systems of pine was larger than that of spruce due to the larger size of the root system.
The respiration rate per unit weight of pine roots of the 1- to 3-year-old seedlings decreases significantly with the increasing age. In spruce, the decrease was smaller. The result could have been different if only the short-roots of the same growing season were studied from all seedlings.
During the first growing season the root respiration rate decreased from the middle of the summer towards autumn. An experiment with pine seedlings grown in the mineral soil showed a very rapid increase in respiration rate in the spring. The rate, especially oxygen uptake, is at its greatest in the roots at the time of fastest growth.
Examination of stands developed under natural conditions can be used to provide basis for comparison for study of the development and yield of stands treated with intermediate fellings. In Finland, the first investigation and the yield and the structure of natural normal stands were published in 1920. This investigation on development and yield of the natural forests of Kainuu in southeastern Northern Finland is based on 92 sample plots on three forest types; Empetrum-Vaccinium type (EVT), Empetrum-Calluna type (ECT) and Vaccinium-Myrtillus type (VMT).
The Scots pine (Pinus sylvestris L.) sample plots represented variation of age classes for construction of mean development series. The Norway spruce (Picea abies (L.) H. Karst.) of the region are so old that development series could be obtained only for dominant trees based on stem analysis.
The average development of Scots pine stand on EMT type within the region is on average more rapid and the yield in cubic volume quantitatively larger and structurally better than that on ECT type. Self-thinning during the early decades of EVT is slower. The pine stands are denser in the age of 70 in Kainuu compared to Central Northern Finland, but the development and yield are similar.
The development, yield and structure of natural Norway spruce stand on VMT proved considerably inferior to the average level of pine stands on EVT, and to a major part on ECT. The mixed pines on spruce sample plots have developed better than spruces of equal age. Spruce stands on VMT in the area developed markedly better than Geranium-Dryopteris-Myrtillus (GDMT) in Central Northern Finland.
It seems that a spruce stand seems to require more fertile site type in north than in the southern part of Finland. These fertile types are relative rare in the north. In the region, the best results are received with pine. As a rule, also the yield of birch (Betula sp.) is poor in the region.
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Growth-promoting effects of enhanced caron dioxide levels upon forest tree seedlings grown in plastic houses was studied in 1964 and 1965 in the Forest Breeding Foundation in Haapastensyrjä near Loppi in Southern Finland. In both years more vigorous height and weight growth, and development of root system was achieved when the CO2 concentration was increased to 0.2% than in the normal conditions (CO2 0.03%). The CO2 concentration was increased by burning propane in the plastic houses. Burning continued for four hours per day either at 8–10 and 14–16 a clock or 6–10 a clock. Growth was not affected by the time of the treatment, and it was equally high in 0.1% and 0.2% concentrations.
Treatment of the seedlings with 100–200 ppm gibberellic acid (GA) increased the height growth of healthy, well-rooted seedlings. Treatment with a concentrated (600 ppm) dosage, as well as treatment with a combination of GA and 1-naphtyl acetic acid (NAA) caused serious defects in grafts of Scots pine (Pinus sylvestris L.). GA treatments did not induce flower formation in pine. Red light during the night seemed to enhance growth of grafts of silver birch (Betula pendula Roth) and Norway spruce (Picea abies (L.) H. Karst.).
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Seed storing experiments with cones of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) were conducted in Oitti seed extracting plant in Southern Finland from February to December 1955. The pine cones were stores for 267 and the spruce coned for 304 days. In four of the storage methods the cones were packed in sacks and another four in wooden boxes. Sample of cones were taken once a month, seeds were extracted and the germinative capacity was tested. The remaining extracted seeds were placed in storage, and in January 1956 moved to cold seed cellar until 1962, when the viability of the seeds was tested.
According to the results, cleaned pine cones can be stores for at least nine months using almost all methods of storage which are commonly used at our seed traction plants, without hazarding the usability of the seeds. The seeds in spruce cones, however, seemed to be more sensitive to conditions during the storage. The germinative capacity of the spruce seeds began to decrease after the beginning of May. Later the seeds were infected with mould, which increased towards the end of the experiment.
Thus, preservation of the germinative capacity of the seeds of pine and spruce requires storage in different conditions. The results suggest that extraction of spruce seeds should be finished during the cold winter months. It seems that seed in the cones of pine and spruce endure storage in piles of paper or cloth sacks at least as well as in wooden boxes. Occasional warming of the storage, snow and foreign material among the cones and an over meter thick cone layer decreased the germinative capacity of spruce seeds during spring and summer. Spruce seeds that had been extracted immediately after collecting of the cones preserved their germinative capacity well during an eight years storage period.
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The aim of this work was to study, on the basis of material published earlier (Heikurainen 1959), the effect of temperature on stand increment, to find out if there is any differences between Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.), and to study the effect of site quality on the relationship between stand increment and temperature. The calculations were based on data collected from 396 sample plots on drained peatlands in different parts of Finland.
There seemed to be no differences due to tree species or site quality in the relative amounts of growth under different climatic conditions. Thus, differences in the absolute growth between poor and fertile sites are noticeably smaller in Northern Finland than in Southern Finland. The author suggests that this implies that the lasting maximal increase of growth which can be produced, for instance, by using soil-improving agents must be less in unfavourable conditions than in favourable.
The aim of this investigation was to clarify aerial infection of Fomes annosus (now Heterbasision annosum) in the cross-sections of stumps of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) in Southern Finland. In addition, an attempt was made to study possibilities to reduce an eventual aerial infection by means of spreading various protecting substances on the cross-section of the stumps immediately after cutting. The stumps were treated withs creosote, ceruse (lead white) and a product named ”Ventti”, which active constituent is copper. The effect of prescribed burning of the site on the aerial spreading of the fungus was studied.
Five sample plots were located in spruce stands and one in a pine stand. One of the spruce stands was prescribed burned. Samples were taken from the stumps 14–17 and 24–29 months after cutting. To identify the fungi, the samples were cultivated on a nutrient substrate in laboratory conditions. The results show that Heterobasidion annosum had spread by air to cross-sections of stumps of spruce. 11.5% of the samples taken from the spruce stumps 14–17 months and 17% of samples taken 24–29 months after cutting were infected. Burning of the site reduced strongly the aerial infection of stumps by the fungus. The stumps of Scots pine were not infected by Heterobasidion annosum in this study. The infection could be limited by treating the cross-sections with substances that are used to prevent growth of mould.
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Mycorrhizal association is a characteristic feature of the trees of the northern coniferous forests. The purpose of the present study was to determine what influence some fungicides and herbicides regularly used in Finnish nurseries have on formation and development mycorrhizal in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) seedlings. The results are based mainly on field experiments in nurseries. First the initiation of mycorrhiza was described in untreated seedlings.
In the first growing season mycorrhizal infection commences fairly late even under normal conditions, i.e. 6–7 weeks after seeding and 3–4 weeks after the formation of the first short roots. Soil disinfectants are commonly used in nurseries before seeding, and they are supposed to evaporate or disintegrate in a few days or 1–2 weeks. In pure culture experiments mycorrhizal fungi proved several times more sensitive than parasitic and indifferent soil moulds to herbicides and fungicides, but in field experiments the delay of mycorrhizal infection caused by them does not seem to harm the seedlings. In the second summer differences of mycorrhizal relations between treated and control plots disappeared. Accordingly, the influence of biocides on mycorrhizae, when applied in the customary concentrations, does not extend beyond the first growing season.
Methyl bromide and SMDC retarded mycorrhiza formation distinctly, while formaldehyde and allyl alcohol had no effect. Apart from not retarding mycorrhizae, formaldehyde and allyl alcohol promoted seedling growth and favoured Trichoderma viride in the soil. Trichoderma is known to be antagonistic to many fungi.
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This paper aims at studying regeneration of Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) by sowing and natural regeneration of birch (Betula sp.) in Western Finland.
Germination of spruce and pine seeds may be prevented by dryness and temperatures below the optimum for germination. In natural conditions, when temperature and moisture is insufficient for germination, the type of seedbed generally has en effect on germination result. Trenching of the seeding spots showed that root competition during the early stage of regeneration was not of decissive importance. It seemed to, however, improve the preservation of the seedlings later. It is common that it can take long before the seeds germinate, and during that time the number of viable seeds decrease strongly.
Also, the seedling stock quickly began to decrease in number after germination, especially during the first growing season and the following winter. The decrease was larger in intact vegetation than on mineral soil or in the humus layer. The emerging seedlings were destroyed by drought very easily, but their tolerance to drought improved later on.
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Prescribed burning has been used in regeneration areas in Finland as a method to treat the humus layer and creating more favourable chemical, physical and biological conditions for the seedlings. At the same time, fire clears away seedlings and shoots of unwanted trees and other vegetation. Direct sowing or planting, mostly Scots pine (Pinus sylvestris L.), seldom natural regeneration, is used. In this paper, the initial stages of the formation of a new tree generation of Scots pine and Norway spruce (Picea abies (L.) Karst.) on prescribed burned areas is studied in Central Finland in 1956–1960.
The burned area remains almost without vegetation for about two growing seasons. Conditions on a burned area which has not been tiled are very unfavourable for germination of seeds of coniferous and deciduous trees. On the other hand, shoots of deciduous trees occur soon after burning. Conditions for regeneration were found to be better 3–5 years after burning. Removal of humus layer in spots improved regeneration. However, the patches facilitated also natural regeneration of Norway spruce and especially birch (Betula sp.), which compete with Scots pine seedlings.
Continuous rainy periods improved the germination of Scots pine and Norway spruce seeds sown on the humus layer. Pine and spruce developed more rapidly on the exposed soil, however, young seedlings were easily destroyed. Seed eaters destroyed the pine and spruce seeds sown on the humus layer of newly burned areas completely or almost completely. The viability of pine seeds sown on the burned humus layer did not decrease for three weeks, but the viability greatly weakened after six or more weeks. Spruce seeds lost their viability faster than pine seeds.
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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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Compression wood of the tree species studied in this investigation, Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) Karst.) and common juniper (Juniperus communis L.), was found to be characterized in its cross section by the thick walls and rounded shape of its tracheids and the profuse occurence of spaces. Tension wood of aspen (Populus tremula L.) and alder (Alnus incana (L.) Moench) was found in microscopic examination to be characterized by the gelatinous appearance of the wood fibres, by its small cell cavities and by the thickness and buckling of the inner layer of the cecondary wall. Tracheids of the compression wood were found to have shorter length than normal on an average, while the tension wood fibres were found to be longer.
The microchemical studies suggest a higher than normal lignin content in compression wood and lower than normal lignin content in tension wood, as compared to normal wood. The reverse would be true for the cellulose contents. Volume weight of absolute dry reaction wood was distinctly higher than that of normal wood. The longitudinal shrinkage of reaction wood, particularly of compression wood, is several times that of normal wood. Transversal shrinkage of compression wood is much less than normal wood. Swelling tests revealed pushing effect of compression wood on elongation and pulling effect on tension wood on constraction. Volume shrinkage of compression wood is less than that of normal wood, in contrast to tension wood. The strength of compression wood in absolutely dry condition was nearly same as that of normal wood.
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In Finland ocular estimation of the growing stock has been made by means of volume tables based on the mean height and density class, or on the dominant height and density class of the stand. The author has observed that if the volume of a stand is estimated by employment of both tables, the results vary markedly from one another. Furthermore, volume of fully stocked stands in the dominant height tables show an approximate correspondence with the volumes of managed normal stands in Southern Finland.
The purpose of this study is therefore to develop volume tables for coniferous trees, based on the density class and the mean height; these tables should give the same volume for a stand as the dominant height tables.
Volume per hectare of 187 Scots pine (Pinus sylvestris L.) stands and 120 Norway spruce (Picea abies (L.) Karst.) stands on different forest types were estimated using the relascope method in Southern Finland. With the volume and the measured mean and dominant heights as a basis, the density classes were extracted from both mean height tables and the dominant height tables. The investigation indicates that the author estimated the dense stands too thinly, and the thin ones too densely, and that the erroneous estimation of the density can be corrected by comparison of the ocular estimations and the corresponding measurements. The density can be measured by means of crown closure, stem number per hectare or the basal area per hectare.
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Snow cover and ground frost was studied in 29 forest stands in Southern and Central Finland in 1957–1959. The tree species influenced greatly accumulation of snow on the forest floor. Norway spruce (Picea abies (L.) Karst.) retains snow in its crown. In addition, snow and water falling from the branches compress the snow cover under the trees, and the ground freezes deeper because of the shallow snow cover. In the spring, the dense crown prevents rain and radiation reaching the ground, which remains cold longer. However, ground frost may protect spruce, which has a weak root system, from wind damages.
Scots pine (Pinus sylvestris L.) has similar, but milder, effects on snow cover within the forest. The crowns of pine seedlings and young trees pass snow easily, but later the crowns intercept it considerably. The lower branches are, however, high up and the snow is evenly spread on the ground. The deciduous trees intercept little snow and in the spring the snow smelts and the frozen soil thaws early. The snow conditions of deciduous forests are, however, changed by a spruce undergrowth.
It can be assumed that the unfavourable conditions in spruce forests can be alleviated by thinning. Also, mixture of pine and deciduous trees can transform the conditions more favourable in the spruce stands.
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Since Finnish professor A.K. Cajander published his theory on forest types, there have been discussion and contradictory studies on certain forest types. This paper is a litterature review on the thick-moss type in Northern Finland and its parallel types in Kainuu and Southern Finland. First, the principles of Cajander’s theory on forest types is described and discussed. It is concluded that Cajander has described forest site types as their common, genuine variants. Borderline variants have been excluded from the description.
Second, the North Finnish thick-moss type (Hylocomnium-Myrtillus type, HMT) and its position in Cajander’s system is discussed. Concepts of this forest type have varied considerably, and it has been argued that the type does not fit Cajander’s system very well, as it arises as a result of the invasion of other forest types by Norway spruce (Picea abies (L.) Karst.) with consequent degeneration of the site.
The writer concludes findings of the results of the previous studies about MHT and its relations to the Myrtillus type. Cajander in his system included the thick-moss type in the moist upland forests as a type whose vegetation is less exacting than that of the Myrtillus type. This position seems to be the right one. Some factors point out the moist nature of HMT: the ability of Norway spruce to compete, a relatively high persipitation, the humidity of the climate in general and the rather poor water percolation capacity of the moraine soil. The HMT sites are relatively poor. It is stated that the opinion that the thick-moss type is secondary state of development of the Myrtillus type has no plant sociological, ecological, mensurational or silvicultural foundation. The type is probably Finland's most dynamic forest type, but in the natural forest its dynamics are confined to such changes as are permitted within the same forest type. HMT must be described as three series of plant association types, which differ from another to some extent.
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This paper deals with two machines designed for abrading seed wings, and their influence on the germinative capacity of seed of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.). Both machines are commonly used in Finland.
The results of the study indicate that the act of abrading may cause slight or even serious injuries to the seed. Slight injuries of about 3% are probably not easily avoided if mechanical abrading is resorted to. It must be noted, however, that even this reduction in germinative capacity causes significant yearly loss. If the reduction in germinative capacity is greater, which seems to be possible, it is advisable to test the mechanism of the machine and its method of abrading. As the clearance of the machines can affect the extent of injuries, all machines should be tested. If possible, a continual operation control should be arranged. It could, at the same time, to supply material for improving the abrading method and equipment.
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Draining transforms root systems of trees growing in peatlands towards the ones growing on mineral soil. However, even after efficient draining the root systems differ from the root systems of trees growing on mineral soil. This investigation concentrates on root systems of forests of similar mire types growing in similar draining conditions but having different tree species compositions. The peatland, situated in Pieksämäki in Southern Finland, was drained in 1937. Sample plots, measured in 1956, consisted of mixed forest of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies L. Karst.) and birch (Betula sp.) in different compositions, and were in natural condition.
The sedge pine bog studied in this investigation was shown to have larger total amount of roots and mycorrhiza than in previously studied dwarf shrub pine bogs. This reflects better growth conditions of the better site. The depth of root system was, however, similar. Root systems of birch were deeper than those of the coniferous tree species. Differences between Scots pine and Norway spruce were small. Corresponding differences between the species were found in the density and total number of mycorrhizas. The abundance of mycorrhizas in the roots of birch increased in deeper layers of peat, but decreased especially in spruce roots. In earlier studies the abundance of mycorrhizas decreased in the roots growing in deeper layers in pure Scots pine stands, but no such variation was seen in this study. The result suggest that the deep root system of birch may affect also the root systems of the coniferous trees. On the other hand, birch roots can have advantage over the coniferous trees.
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In this investigation was studied 1) Volume growth and yield of timber in managed Norway spruce (Picea abies (L.) Karst.) forests under different rotations. 2) Value growth, net forest income and soil expectation value of managed forests under different rotations, and 3) The rotations of spruce forests managed on different rotation principles. The data was collected from Oxalis-Myrtillus type forests in South-West Finland.
Two developmental series of stands were constructed for the research, one of which were of better sites than the other. Sample plots were pure, even-aged spruce stands in well-managed forests. The stands had been thinned from below. The age varied from 25-30 years to the age of final cutting.
According to the study, in the artificially regenerated spruce stands the highest mean annual volume growth, 9.7 m3/ha, and also the highest net annual income of 14,50 Finnish marks/ha (calculated from average stumpages) was reached in rotation of 70 years. In the other managed spruce forests a mean annual volume growth of 6.6-8.8 m3/ha and the net annual income of 10,500-14,500 Finnish marks/ha were reached in the rotation of 70-100 years. The rotation for the maximum mean annual volume growth varied in the different series between 67-92 years. The maximum mean annual forest rent was only achieved in series B in a rotation of about 100 years, and in a naturally normal stand in a rotation of about 120 years. The intensity of thinnings and silviculture had a greater effect on value growth and on net income than on volume growth.
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Bark beetle populations live usually in a balance in natural forests, and outbreaks occur seldom. The populations have been found to increase in managed forests. Fellings affect the structure of the forests, which influence the living conditions of the insects, and produce material for reproduction. In this study the occurrence of bark beetles was studied in a forest area in Etelä-Häme in Southern Finland using line plot survey.
The forests in the area were Norway spruce (Picea abies L. Karst.) dominated. Over third of the 140 sample plots studied were in forests which had never been cut or it was over ten years to the last logging. Bark beetles of 26 different species were found in 66 of the sample plots. The most common species was six-toothed spruce bark beetle (Pityogenes chalcographus L.), which was due to the abundance of growth material suitable for the species in the area. New species in the area were common double-eyed spruce bark beetle (Polygraphus polygraphus L.), Pityophthorus micrographus L., and Dryocetes-beetle (either Dryocetes autographus or D. hectographus). The fellings increased the occurrence of beetles. The amount and quality of logging residue affected the abundance of the insects.
The PDF includes a summary in German.
The cone crop of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) has been assessed in Finland since 1930 annually by sending a questionnaire to forest professionals around the country. Based on the result it is decided if the crop is good enough for collection of the cones next winter. This article presents the results of cone surveys in 1950-1953, and suggest improvements in the method of the investigation.
According to the survey, Scots pine crop was best in 1952, when the crop was intermediate in the whole country, and relatively abundant in the county of Lapland. Norway spruce crop was best in 1951, when the crop was better than in average in the whole country. The evaluators had variable opinions whether the crop was good enough for cone collection or not. They assessed the pine cone collection more often as profitable than the spruce cone collection. Usual reasons to regard spruce cone collection as unprofitable were seed damages and the sites being too far away. To make the results more uniform and accurate, a suggestion to change the evaluation method is presented. The evaluation should be focused on the cone crop of mature stands.
The Acta Forestalia Fennica issue 61 was published in honour of professor Eino Saari’s 60th birthday.
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Norway spruce (Picea abies (L.) Karst.) invading sites is common in Finland. The species tends to establish itself as undergrowth, and takes over when it gets space to grow. To determine whether the undergrowth is suitable as the new generation requires knowledge on the biology of spruce undergrowth. One of the issues is determining the age of the stunted trees. In this investigation, 100 undergrown spruce trees, their crown and their root systems were studied. A method was developed to determine the age of the trees.
The root system of all trees in Vaccinium sites and of stunted trees in Myrtillius sites were superficial. The root systems of older spruces were purely of adventitious origin. The longer the period of stunting growth, the younger is the root system. In addition to acropetal and general adventitious ramification there is often adventitious branching of the roots of pathological causes. Mortality among the long roots is frequent.
A stunted tree has not the same ability as a viable tree to make use of already existing branches for building assimilating surface. When comparing trees with equally large assimilating surface, a stunted tree had greater sum of roots compared to a viable tree. The root system of a stunted undergrown spruce was very superficial compared with the other trees.
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The purpose of the investigation was to study the amount, quality and distribution by layers of depth of horizontal roots in Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) stands in Southern Finland. The sample plots included stands on soil varying from sandy to stony, and stands of varying ages from seedling stands to an old stand, in Myrtillus and Vaccinium type forests.
In a Norway spruce stand, the amount of roots increases rapidly and reaches its maximum, about 450 meters/m3, at an age of 100-110 years. In a Scots pine stand the maximum, about 370 m/m3, is reached earlier, at an age of 60-70 years. The root system of pine expands more rapidly than that of spruce. The total length of the horizontal root system of pine amounts to 1,000 m soon after 40 years of growth, of spruce at the age of 60. Later the situation changes, and at the age of 110 the root systems of both species are about the same size, but older trees of spruce have more extensive root system.
Majority of horizontal roots are under 1 mm in diameter. Of the horizontal roots of spruce stands the majority lie in the humus layer and in the topmost mineral soil stratum. Over half of horizontal spruce roots are, thus, at a maximum depth of 5 cm, while majority of the roots of Scots pine lie at maximum in depth of 10 cm. At the same layer grow also the roots of the ground vegetation, which may affect the competition between the species.
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The different kinds of injuries in Norway spruce (Picea abies (L.) Karst.) stands was studied in 52 sample plots in Peräpohjola in the northernmost Finland. The age classes of the stands varied from 100 years to over 220 years. Most of the stands were unevenaged, as is usual in the area.
In the younger age classes (121-160 years) majority of the trees were of normal quality or had smaller injuries in all forest types. In age classes over 160 years the trees of merchantable quality decreased markedly in all forest types. The quality of the trees decreases with the age especially because of butt rot, braking of trees and crooks, forks and heart and top decay caused by the injuries. To ensure future quality it would be important that the stand is healthy from the beginning. When old spruce stands of the area are in large extent diseased by the root rot, it is questionable if they can be regenerated using natural regeneration. The spruce stands of the area are also relatively branchy. This could be prevented by growing the young stands dense. Changing the dominant tree species to Scots pine (Pinus sylvestris L.) in the dry upland forest sites could be a way to improve the quality of the forests in the area.
The PDF includes a summary in German.
Observatons of drying of Norway spruce (Picea abies (L.) Karst.) stands increased in 1930s in Southern Finland. The aim of the study was to analyse the advance and causes of drying. The work was begun in 1930s before the Second World War, and the damages caused to the forests by the war was used as supplemental observations in the study. A special method, drying analysis, was developed to study the process. It was used both in cases of insect and fungal diseases in the four research areas in Raivola and Ruotsinkylä. In addition, 7 observation areas were studied.
Several causes for drying of the trees were observed in the Norway spruce stands. These included European spruce bark beetle (Dendroctonus micans), root rot (Heterobasidion annosum), pine weevils (Pissodes sp.), bark beetles and honey fungus (Armillaria mellea).
The role of primary and secondary causes for drying, resistance of the trees and the drying process are discussed. Finally, the influence of forest management in drying process is analysed. Forests in natural state can be considered to be in an ideal balance. On the other hand, forest management can be used to maintain the vitality and resistance of the forests. Drying of Norway spruce stands can be taken into consideration when the stands are managed.
The PDF includes a summary in German.
The aim of the investigation was to study natural regeneration of Norway spruce (Picea abies (L.) Karst.) in drained peatlands and frost injuries in seedlings, and to compare microclimates of the regeneration areas. The experiments included peatlands in Satakunta in Western Finland. Restocking of the areas with seedlings and their survival was followed in 1935-40 at sample plots that were mainly 1 are large.
Susceptibility to freezing was shown to be dependent on the stage of development of the shoots. Shoots that have just begun to grow contain little water, and withstand better freezing temperatures than shoots in later stages of growth. Damages to the seedlings were observed when the temperatures decreased to -2.8–-4.3 °C. The most severe damage to a seedling was caused by the death of the leading shoot by spring frost.
Norway spruce regenerates easily on moist peatlands, but peatlands with dry surface tend to have little or no seedlings. The species regenerated better in marshy sites than correspondingly fertile mineral soil sites. However, it needs shelter to avoid frost damage. On clear cut spruce swamp the undergrowth spruce seedlings that were left in the site got severe frost damage. If the site had birch (Betula sp.) coppice or undergrowth, spruce seedlings survived in their shelter depending on the height and density of the birch trees. To be effective, the protective forest should have relatively even crown cover. Young spruce seedlings could grow well even under relatively dense birch stand.
The PDF includes a summary in German.
The tree canopy adsorbs part of the rainfall falling on a forest, therefore only part of it reaches the soil. This report presents results concerning interception of precipitation and groundwater level in forests of varying canopy cover. The study belongs to a larger survey on afforestation of drained treeless bogs. The rainfall was measured daily in the open fields and in the adjacent forests. The forests, mainly Norway spruce (Picea abies (L.) Karst.) dominated, were divided by the canopy cover into five classes from over dense to sparsely stocked.
The results show that in a dense, tall Norway spruce stand, light rainfall can almost entirely be adsorbed by the canopy. The heavier the rainfall, the larger proportion of it reaches the ground. Only 30% of a 5 mm rainfall reaches the ground, while 80% of a 20 mm rainfall reaches the ground. Interception of precipitation decreases gradually when the density of the forest decreases. Canopy of Scots pine (Pinus sylvestris L.) and birch (Betula sp.) stands of corresponding density adsorb less rainfall than Norway spruce canopy. Groundwater level was higher in treeless areas than in areas covered with forest. Widescale clear cuttings should, therefore, be considered carefully in forest areas that are prone to become peaty.
Of the foreign tree species Siberian larch (Larix sibirica Ledeb.) has the biggest economical potential in Finland. In its natural distribution the species grows mostly in mixed stands in other areas than the core of its range in Siberia, where it grows also in pure stands. However, growth studies have given contradictory results about how Siberian larch can manage competition of different tree species in mixed stands. In this study two-year old Siberian larch seedlings were planted in areas previously sown with Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.). The growth of the trees was measured when the stands were 50 years old.
It appears that the stands, about 3700 larch seedlings per hectare, have originally been too been too dense. In the two thinnings done in the area, larch has probably been favoured, which has resulted in varying mix of pine and spruce. In the 50-year old stands, Siberian larch has developed faster than Scots pine and Norway spruce. Contrary to some previous studies, the results show that Siberian larch can be grown also in mixed stands, but the growth will probably be slower than in pure stands. Best growth is achieved in pure stands that have been planted thinly enough.
The PDF includes a summary in German.
The aim of the study was to investigate effect of growth conditions on germination and growth of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) seedlings in greenhouse conditions. Germination of seeds becomes markedly slower as the soil temperature decreases. It seems that low temperatures affect more Norway spruce than Scots pine. When temperature rises, the fresh weight of the seedlings increases more in pine seedlings than in spruce seedlings. Accordingly, lower temperatures affect less the weight growth of spruce seedling than that of pine seedlings.
An experiment testing how root competition affect germination showed that adjacent seedlings decrease germination of seeds more than shading with branches. The effect was strongest on pine and spruce seedlings when the shading tree species was fast growing birch (Betula sp.). On the other hand, shading affected most height growth of birch seedlings. Growing space can vary in relatively large range without it affecting greatly tree growth.
The PDF includes a summary in German.
The most important characteristics for the quality of round timber is knottiness. Knots decrease the strength of the wood in sawn goods. Knots in pulpwood obstruct the production process of ground pulp and lower the quality. A qualitative classification of saw logs has been suggested, and the abundance of knots could also be used to determine the quality of pulpwood. In this study, visual observations on the preparation of pulpwood in pulp mill were made to observe the quality of the wood. Samples of the wood was collected, and they were divided in five quality classes. To study the influence of age, forest site type and stand on knots, 140 sample trees of Norway spruce (Picea abies (L.) H. Karst.) were analyzed. The article includes detailed analysis of the abundance and position of knots in the stems of spruce, anatomical structure of the knots, microscopic structure of the fibers, and mechanical properties of the branch and knot wood.
The drained peatlands regenerate usually well, and artificial regeneration by sowing or planting has been rare. Field trials of Norway spruce (Picea abies (L.) H. Karst.) were established in northern Satakunta in Western Finland in three drained peatlands in 1934. Sowing trials of Norway spruce consisted of patch and broadcast sowed sample sites in treeless bogs and under protective forest. The seedlings of spruce were planted either under protective forest or in treeless peatland.
The results show that artificial regeneration of Norway spruce succeeds best under protective forest. The best tree species for upper storey is Betula sp. which grows fast and controls growth of ground vegetation. The peat is relatively decomposed on those peatlands that are suitable for spruce, and breaking of the surface of the peat is not recommended. In the sowing trials, breaking of the upper layer of the peat caused frost heaving, cracking of the dried surface and sticking of mud in the seedlings in the patch sown sample site. The shoot and root growth of seedlings of the broadcast sown site was better than seedlings of the patch sown site. The planted spruce seedlings seemed to be more susceptible for spring frost than the seedlings in the sown site. The plants of seed origin succeeded in general better than the planted seedlings.
The PDF includes a summary in German.
Natural regeneration has been common in Northern Finland, where forest fires have been usual, and the large areas make artificial regeneration expensive. The regeneration, and for instance tree species composition and density of the stand, cannot been controlled. In Northern Finland there is little demand for Betula sp. which is often abundant in the burnt areas. The unburned forests are generally Scots pine (Pinus sylvestris L.) or Norway spruce (Picea abies (L.) H. Karst.) dominated mixed forests with single Betula sp. trees.
The fire destroys birch for the most part in the Vaccinium site type, but the surviving trees produce enough seeds to regenerate the areas. The largest trees of Scots pine usually survive the fires. Pine has good seed years in the north only every 8th or 10th year. Spruce is totally destroyed in the forest fire and the seedlings grow poorly as primary species. The seedling stands are usually dominated by Scots pine and birch, but birch seedlings grow in batches, and do not hinder growth of pine. The drier Calluna site type stands are dominated by Scots pine. Birch seedlings may be abundant in the beginning, but most of them do not survive. Abundant emergent pine trees prevent the growth of seedlings especially in the dry site types, and they should be thinned to guarantee regeneration. Sowing results are better few years after the fire. The birch seedling should be removed from the seedling stands.
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Shifting cultivation, practiced earlier in Finland, was beneficial for grey alder (Alnus incana (L.) Moench). It can produce seeds early and the early growth of the seedlings is fast. Areas where shifting cultivation was intensive, the areas next to the fields were pure alder stands, next circle was Betula sp. dominated, beyond that could be found Scots pine (Pinus sylvestris L.), and finally Norway spruce (Picea abies (L.) H. Karst.). When shifting cultivation ended, Norway spruce became more common. Many young mixed stands had Norway spruce undergrowth and alder overgrowth. The aim of the study was to find out how the stands develop to spruce dominated stands, and how they should be managed.
The density of spruce undergrowth affects the further development of both spruce and alder. The number of alder stems decreases the faster the denser the spruce undergrowth is. Alder overgrowth slow down the early diameter and height growth of spruce compared to pure stands. Also the diameter and height growth of alder remains smaller in mixed stands. The basal area of spruce develops slowly in the beginning, increases significantly by the age of 30, and surpasses the growth of pure spruce stands in Oxalis-Myrtillus site type. Thus, Norway spruce do not suffer from growing in the undergrowth. In the first years, fast growing alder seedlings limits growth of ground vegetation and protects spruce seedlings from frost. Later thinning or removal of alder benefits spruce growth. The density of spruce undergrowth decides how much alder can be leaved in the stand. If the spruce undergrowth is thin, more alder can be left in the stand.
The PDF includes a summary in German.
Norway spruce (Picea abies (L.) H. Karst.) is a species that becomes in Finland over time the dominant species in the sites that are suitable for it. The reason that it covers only a quarter of the forest areas in Finland depends mainly on forest fires. The aim of this review was to discuss the biological factors that affect competition between Scots pine and Norway spruce.
Especially important is the ability to regenerate and grow past seedling stage. There does not seem to be significant differences in the number of good seed and seedling years of the species. Spruce regenerates better on moss covered forest floor than pine. On the other hand, pine seedlings grow faster than spruce seedlings, and tolerate better dry conditions. Consequently, one of the defining biological differences is that Norway spruce needs more humid conditions than Scots pine. Spruce is shown to have greater transpiration than pine. Spruce also has higher site requirements, however, growing as undergrowth, it seems to be better able to compete of the nutrients with the larger trees than pine. It also tolerates shading better. Spruce is less frost tolerant than pine.
The PDF includes a summary in German.
Healthy, straight, more or less free from branches and slowly tapering stems are good raw material for woodworking industry. The aim of the study was to investigate, from the stand point of forest management, the influence of stand and forest site type on the technical quality of the stems. Sample plots were measured in Norway spruce (Picea abies (L.) H. Karst.) stands in Eastern Finland. Norway spruce growing in a stand with closed crowns developed thin branches and self-pruned, if the stand was dense in the early stages. The decisive time for the stand is, therefore, when it is at seedling stage and young stand. The stems are more branchy if the stand has been planted. The adequate planting density is discussed based on earlier studies. The sufficient density seems to be achieved when the spacing is at maximum two meters. When the stems are branchless up to four meters, thinning of spruce stand does not affect knottiness or stem form. A sparsely stocked, knotty young stand does not produce good-quality timber even if the stand is later dense. Selective thinning from above can be used to improve the quality of the wood.
The PDF includes a summary in German.
The development roots of Norway spruce (Picea abies (L.) H. Karst.) seedlings was studied in sample seedlings grown in different kinds of sites. In the early stage, the seedling roots grow primarily length. The main root is usually long. If the growth of the root is hindered, the tip of the root dies, and the root system growing from the original root collar remains relatively small; in these cases, the secondary root system becomes more important. In unfavourable conditions the root branches can early on replace the main root. The main root of a germling seems to be less able to seek for free growing space than the main and side roots of older seedlings. When the growth of the root is blocked by some kind of obstacle, it does not often hinder the growth of the seedling. The type of soil influences strongly how the root system grows. In good soil and in humus the root system is regular and richly branched, while in clay and coarse sand the root system was small. Spahgnum moss was good substrate for seedlings, Dicranum undulatum moss little less good, while the seedlings grew poorly on Pleurozium Schreberi.
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The paper presents preliminary results of paleobotanical studies on vegetation in Åland, south-west Finland. The investigations concentrated on studying arrival of tree species and stratigraphy of peatlands. According to the studies, some plant fossils found in the peat (Ceratophyllum submersum, Sparagnium neglectum, Najas flexilis) indicate that climate of the region has earlier been warmer than at the present. The present forests in Åland are dominated by coniferous species, but the pollen analysis of the peat indicate that Norway spruce (Picea abies (L.) H. Karst.) became a common species in the region about by the time of Christ’s birth. The species has reached its present distribution in Åland relatively late. The pollen analyses give relatively little information about the arrival of birch (Betula sp.) and Scots pine (Pinus sylvestris L.), but it seems obvious that occurrence of birch reached its culmination just before spruce. During the warm period common alder (Alnus glutinosa (L.) Gaertn.) was the most important species, and also pollen of oak (Quercus robur L.), kinden (Tilia cordata L.) and elm (Ulmus sp.) was relatively common in the peat of some of the studied peatlands. An interesting finding was the pollen of Carpinus betulus in many sites in Åland.
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The aim of the study was to determine the effect of grazing of the cutting areas to the ground vegetation and regeneration of spruce. The cutting areas could be divided into two kinds of areas based on the vegetation. Hillocks were drier and poorer than other parts of the cutting areas. Their vegetation did suffer less from grazing than the other parts of the cutting areas. The shade-loving plant species decreased, but as the poorer sites have less edible plants, cattle caused less damage than in the better sites. The even spaces between the hillocks had both positive and negative changes. Cattle transport seeds, tile and fertilize the soil, promote paludification, and decrease competition by the primary species like large grasses. This is beneficial to new species. Grazing is directed to large grass species like Calamagrostis. Those species that cattle reject, become more abundant. Stamping damages especially shallow rooted species and perennial species, like Norway spruce (Picea abies (L.) H. Karst.). Larger tree seedlings may get injuries in the stem.
The PDF includes a summary in German.
A big storm hit Finland in 12.10.1933, and caused forest damages especially in the coasts of the Gulf of Finland and Baltic Sea, and in the eastern part of the country. In these areas the wind felled about 75,000‒85,000 m3 timber trees in the state lands. The extent of the wind damage was measured in forest area of 1,500 hectares in Lapinjärvi in Southern Finland. The wind had felled 42% of the Scots pine (Pinus sylvestris L.), 70% of the Norway spruce (Picea abies (L.) H. Karst.) and 44% of the Betula sp. trees. Thus, Norway spruce had been most susceptible for wind damage. That extensive damages in Norway spruce seed tree stands risk the regeneration in the area. Natural regeneration of Norway spruce using seed trees may, therefore, be questioned. The seed tree areas on hills, and especially hollows next to the hills were susceptible for wind damage. A denser border stand protects sparsely stocked seed tree area. The damages were also smaller in older seed tree areas, where the trees and ground vegetation had had time to recover after the felling. The felled spruce and birch trees had often stem rot.
The PDF includes a summary in German.
The abundance of Norway spruce (Picae abies (L.) H. Karst.) undergrowth is common for the state forests in Karelia near the Russian border, in Finland. In the survey, the occurrence of the undergrowth was studied. The article includes a review on the ownership of the forest, forest soils in the area, and the state of forests in the area. Scots pine (Pinus sylvestris L.) is the dominative species in 67%, Norway spruce in 27% and Betula sp. 6% of the state forests. Only 2% of the forests are 1‒20 years of age. Stands in the age group of 61‒80 years are the most common (25%). Norway spruce undergrowth is most abundant in the municipality of Salmi. The forests are typically moist forest site types or grass-herb site types. If the stands are allowed to develop naturally, even the Vaccinium sites become Norway spruce dominated. Spruce undergrowth is formed seldom under a spruce forest unless the stand is thin or has openings. Because Norway spruce is often rare in the mineral soil sites, the undergrowth is often regenerated from seeds that spread from spruce swamps. Earlier practiced shifting cultivation and its frequent fires prevented regeneration of spruce undergrowth. Similarly, the common felling method used, clear felling in strips, does not promote spruce undergrowth. Consequently, their occurrence is likely to decrease in the future.
The PDF includes a summary in German.
The height growth of Scots pine (Pinus sylvestris L.) seedlings were observed in Korkeakoski and Evo in Southern Finland in 1925-1928. The growth was slow in the beginning of the growing season, increased after that to decrease again towards the end of the growing season. The height growth begun in May, reached the fastest growth rates in June, and ended in June-July. According to the earlier studies, the length of the height growth of Scots pine is dependent on the temperature of the previous summer. This study showed that warm temperatures of the same summer promote height growth, and low temperatures slow it down. Also the daily growth fluctuates, being highest during the afternoon and slowest during the early morning. The daily growth is dependent on temperature.
Norway spruce (Picea abies (L.) H. Karst.) begin the height growth in average 9 days later than Scots pine. Compared to pine, the speed of growth in spruce decreases slower towards the late summer.
The volume 34 of Acta Forestalia Fennica is a jubileum publication of professor Aimo Kaarlo Cajander. The PDF includes a summary in German.
There is little knowledge about the value increment of the stands that are about to become mature for felling. Sample plots were measured in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) stands in the most common forest site types in Rovaniemi, in northernmost Finland. Sample trees were chosen from dominant and codominant trees of the stand.
The value increments for the stands were generally very low. The average rotation of the studied stands would be 160 years. In the better forest site type, the increments of basal-area, volume and form height decrease slowly as the diameter of the tree increases. The value increment can give valuable information for intermediate fellings. They should be targeted mainly to large codominant trees and partly also in dominant trees that do not yet give logs, because their value increment is low.
The PDF includes a summary in German.
The first proper growth and yield tables were prepared in Finland already in 1872, but they have been used little as the needs of forestry and forest sciences increased. One of the problems of the old yield tables was how the site quality classes are determined. The new growth and yield tables use the forest site type classification, which enables the use of same site types for all tree species. This makes it possible to compare the growth of different tree species in same kind of sites. The tables also use stem frequency distribution series. In the first stage, the tables were prepared for Southern and Central Finland.
The PDF includes a summary in German.
Norway spruce (Picea abies (L.) H. Karst.) forests in Northern Finland are situated mainly in the state lands. The survey is based on silvicultural surveys made in the northernmost districts of the state forests. The quality of private lands of the area was deduced based on the adjacent state lands and specific observations. A map was drawn on the distribution of productive Norway spruce forest in the study area.
The continuous Norway spruce forest areas covered 1,112,000 hectares, of which 866,000 hectares were on the state lands. Especially in the northern parts of the area also more fragmented spruce forest could be found (130,000 hectares in the state lands). The estimated total volume of the wood in the forests in the state and private lands was 57.78 million m3 in the continuous spruce forest area. The spruce forests were often situated on hill and fell areas relatively high above the sea level. In the areas north of the 66th parallel, almost half of the forests were above 300 meters above the sea level. Because spruce forests of the state lands were concentrated near watershed areas, the wood harvesting was more expensive, and reduced the value of the state forests. The spruce forests grow usually on fresh mineral soil sites. However, towards north the species was found on drier sites. The stands were mostly pure spruce stands or mixed birch-spruce stands. The older age groups were the most common, but young stands were rare.
In the first part of the study, the selected wood and fiber properties were investigated in terms of their occurrence and variation in wood, as well as their relevance for thermomechanical pulping process and related end-products. It was concluded that the most important factors were the fiber dimensions, juvenile wood content, and in some cases, the content of heartwood being associated with extremely dry wood with low permeability in spruce. The following pulpwood assortments of which pulping potential was assumed to vary were formed: wood from regeneration cuttings, first-thinnings wood, and sawmill chips.
In the experimental part of the study, the average wood and fibre characteristics and their variation were determined for the raw material groups. Subsequently, each assortment – equalling about 1,500 m3 roundwood – was pulped separately for 24 h period. The properties of obtained newsgrade thermomechanical pulps were then determined.
Thermomechanical pulping (TMP) from sawmill chips had the highest proportion of long fibres, smallest proportion of fines, and had generally the coarsest and longest fibers. TMP from first-thinned wood was the opposite, whereas that from regeneration cuttings fell in between these two. High proportion of dry heartwood in wood originating from regeneration cuttings produced a slightly elevated shives content. However, no differences were found in pulp specific energy consumption. The obtained pulp tear index was clearly the best in TMP made from sawmill chips and poorest in pulp from first-thinned wood, which had generally inferior strength properties. No big differences in any of the strength properties were found between pulp from sawmill residual wood and regeneration cuttings. Pulp optical properties were superior in TMP from first-thinnings. No noticeable differences were found in sheet density, bulk, air permeance or roughness between the three pulps.
The most important wood quality factors were the fibre length, fibre cross-sectional dimensions and percentage juvenile wood. Differences found in the quality of TMP assortments suggest that they could be segregated and pulped separately to obtain specific product characteristics and to minimize unnecessary variation in the raw material and pulp quality.
Anthesis was studied at the canopy level in 10 Norway spruce (Picea abies (L.) H. Karst.) stands from 9 localities in Finland was studied in 1963-74. Distribution of pollen catches were compared with the normal Gaussian distribution. The basis for the timing studies was the 50% point of the anthesis-fitted normal distribution. Development was characterized in calendar days, in degree days (>5°C) and in period units. The count of each unit began on March 19 (included). Male flowering in Norway spruce stands was found to have more annual variation in quantity than in Scots pine (Pinus sylvestris L.) stands studied earlier.
Anthesis in spruce in Northern Finland occurred at a later date than in the south. The heat sums needed for anthesis varied latitudinally less in spruce than in pine. The variation of pollen catches in spruce increased towards north-west as in the case of Scots pine. In the unprocessed data, calendar days were found to be the most accurate forecast of anthesis in Norway spruce. Locally, the period unit could be a more accurate parameter for the stand average. However, on a calendar day basis, when annual deviations between expected and measured heat sums were converted to days, period units were narrowly superior to days.
The geographical correlations respected to timing of flowering, calculated against distances measured along simulated post-glacial micgation routes, were stronger than purely latitudinal correlations. Effects of the reinvasion of Norway spruce into Finland are thus still visible in spruce populations just as they were in Scots pine populations.
The proportion of the average annual heat sum needed for spruce anthesis grew rapidly north of a latitude of ca. 63° and the heat sum needed for anthesis decreased only slightly towards the timberline. In light of flowering phenology, it seems probable that north-western third of Finnish Norway spruce populations are incompletely adapted to the prevailing cold climate. A moderate warming of the climate would therefore be beneficial for Norway spruce. This accords roughly with the adaptive situation in Scots pine
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A nonlinear programming algorithm was combined with two individual-tree growth simulators consisting of distance-independent diameter and height growth models and mortality models. Management questions that can be addressed by the optimization model include the timing, intensity and type of thinning, rotation age, and initial density. The results were calculated for Norway spruce (Picea abies (L.) H. Karst.) stands on Oxalis-Myrtillus site in Southern Finland, where the stand density after clearing of a seedling stand is about 2,000 trees/ha.
The optimum thinning programs were characterized by late first thinnings (at dominant height of 15–17 m) and relatively high growing stock levels. It was optimal to thin from above, unless mean annual increment was maximized instead of an economic objective. In most cases, the optimum number of thinnings was two or three. Compared to a no-thinning alternative, thinnings increased revenues by 15 –45% depending on the objective of stand management. Optimum rotation was strongly dependent on the interest rate.
Hooke and Jeeves’ direct search method was used for determining optimum solutions. The performance of the optimization algorithm was examined in terms of the number of functional evaluations and the equivalence of the objective function values of repeated optimizations.
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The present paper deals with the effects of clearcutting on soil and air temperature and the development of temperature conditions during the 12 growing seasons following clearcutting of a Norway spruce (Picea abies (L.) H. Karst.) stand on a Vaccinium-Myrtillus forest type in Kainuu, northeast Finland. The uncut control site had a growing stock of 140 m3/ha. The temperature measurements were carried out by means of thermographs, Grant measuring devices and minimum and maximum glass thermometers.
Clearcutting had no significant influence on temperatures measures at 2 m above the ground in a meteorological screen and no changes occurred in them during the period studied, while on the ground level and in the adjacent layer of air the daily maxima increased and the daily minima decreased as compared with uncut forest. The greatest difference was over 10°C between the maximum temperatures at 10 cm and almost 8°C between the minimum temperatures. Night frosts were considerably more common at 10 cm above the ground in the clearcut area than in uncut forests.
Temperature differences were smaller in the soil than close to ground level. Day temperatures were 2–3°C higher in the clearcut area than in uncut forests, and differences between night temperatures at this depth were even smaller. Correspondingly, temperatures were 3–5°C higher at depths of 50 cm and 100 cm in the clearcut area during the whole measuring period. The differences between the temperatures in the clearcut area and uncut forests did not diminish to any significant extent during the 12 years despite the stocking of the former area with seedlings.
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The premises of several models obtained from literature on bud dormancy release in trees from cool and temperate regions differs from each other with respect to responses to air temperature during the rest period of the buds. The predicted timing of bud burst in natural conditions varied among the models, as did the prediction of the models for the outcome of a chilling experiment.
Experimental results with two-year old seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) did not agree with any of the models. The experimental results also deviated from abundand earlier findings, which also disagreed with any of the models. This finding suggests that Finnish provenances of Scots pine and Norway spruce differ from more southern provenances with respect to temperature regulation of bud dormancy release.
A synthesis model for the effects of air temperature on bud dormancy release in trees was developed on the basis of the previous models and the experimental results of both the present and previous studies. The synthesis model contains part of the original models as special cases. The parameters of the synthesis model represent several aspects of the bud dormancy release of trees that should be addressed separately with each species and provenance in experimental studies. Further aspects of dormancy release were discussed, in order to facilitate further development of the models.
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The aim of the present study was to evaluate and develop the use of natural regeneration of Norway spruce (Picea abies (L.) H. Karst.) in private forestry. The study was carried out using a line-plot survey with permanent circular sample plots. In total 40 regeneration sites were measured. The study includes results from three successive inventories: prior to the shelterwood cutting, in the summer after the cutting, and one year after the cutting. Regression and logistic regression analyses were used to construct models describing the effect of various factors on the restocking of the stands.
The standing volume prior to the shelterwood cutting was on average 236 m3/ha (ranging from 80 to 428 m3/ha) and after the cutting 120 m3/ha (39–220 m3/ha). The average number of stems per hectare decreased from 435 to 186. Prior to the shelterwood cutting 22% of the stands were satisfactorily restocked. After the cutting and one year later these percentages were 6 and 29%, respectively. Prior to the shelterwood cutting the number of acceptable seedlings was 1,440/ha, in the summer and year later 1,308/ha and 1,546/ha, respectively. Prior to the shelterwood cutting the characteristics of the mother stands did not correlate well with the number of seedlings. The change in the number of seedlings during the initial stage of shelterwood method depended on height of the seedling stand, amount of logging waste and number of germlings prior to the cutting. The risk to fail in regeneration was highest in the poorly restocked, sparse shelterwood stands, where a fast expansion of grass vegetation took place.
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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.
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The paper concerns relationship between climatic factors and annual ring indices mainly in Southern Finland. The studied index series were from papers of different authors and from different localities. The monthly mean temperatures and precipitation sums were derived from the measurements of meteorological stations. Effective temperature sums for different periods of the year were calculated from the monthly mean temperatures.
The autocorrelation functions were estimated for each index series. The autocorrelations at lag I were significant except for one series. Altogether the differences in the structures of the index series were noticeable, especially between the Scots pine (Pinus sylvestris L.) index series. The influence of climatic factors on the annual ring index variation was studied using cross correlation analysis, simple distributed lag models and transfer function-noise models.
The decisive factor for the annual ring index variation of Norway spruce (Picea abies (L.) H. Karst.) appears to be the effective temperature sum of the growing season. Warm periods during latter parts of previous summer had a negative effect on indices. For the variation of the Scots pine indices the most important climatic factors were the effective temperature sum of the latter part of the growing season and, especially on the arid sites, the precipitation sum during May-July.
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The paper is the final report of a study on the estimation of value increment and inherent variables of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) stands. The main aim was to obtain improved criteria for decision-making concerning the priority of stands for regeneration.
The construction of various estimation models and their reliability are discussed in detail. The study, together with some previous papers, has resulted in a system which on the basis of a number of easily assessed stand variables gives for the stands concerned the volume of stems, percentages of timber assortments, stumpage value, volume increment and value increment.
The following examples are given with regard to the practical application of the results, in addition to the determination of the relative maturity of stands: 1) The study of various trends in stand development; the comparison between the volume and value variables. 2) The estimation of timber assortments needed for a cutting budget, trees marked for felling etc. 3) The calculation of the value of forests.
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Variation in the radial growth of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) was studied in 10 localities in Southern Finland. The aim of the study was to utilize the information on variation in the growth indices for growth estimation, and to evaluate the relative accuracy of growth estimation based on the data from increment boring, in comparison to other methods.
The climatic variation in periodic growth (5-year-period) in Southern Finland is about 11% of the normal level. The results suggest that the data from 10 localities can be used in the computation of the index series for Southern Finland and that the data from 10 relascope plots are required in the study of the climatic variation in tree growth in a given locality. The standard error of the estimate in actual growth estimation for past and future periods by the stand function method is about 23%, the errors of the method involving increment boring being 6% and 16% respectively in past and future growth estimation. The respective methods yield about 20% and 13% error in average growth estimation. With aid of the average growth indices for Southern Finland in local growth estimation the accuracy is distinctly improved, the error being equal to 12% only, while the accuracy in other cases is slightly improved.
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The paper concerns the estimation of the increment of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) stands in the southern half of Finland. For the methods based on stand tables, tree functions forecasting the annual increment of diameter and height during the next 5-year period are presented. The main results of the study, however, are the functions for the volume increment percentage of pine and spruce stands. The independent variables are: forest site type, tree species, stand age and volume, and mean diameter. The standard error of estimate is about 17% in the best functions. Calculations were made also with regard to the application of the results in growth estimation of large forest areas.
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The net photosynthetic rate per unit of foliage was studied in two-year old cuttings of Norway spruce (Picea abies (L.) H. Karst.), representing four clones, at varying temperature and soil moisture. The CO2 compensation point (Γ), photorespiration, dark respiration, and water balance were also investigated. All these characteristics indicated differences among the clones. A correlation between CO2 exchange and transpiration suggested that stomatal control determined at least a part of this variation during a favourable water balance. An inverse relationship existed between Γ and net photosynthetic rate, and the same curvilinear model explained this variation in unstressed as well as stressed plants at a given temperature. An increase in Γ seems to be a normal result of water stress, particularly at high temperature, indicating an increase in mesophyll resistance to CO2 diffusion. This result was in agreement with calculated values of mesophyll resistance. It also supported our earlier conclusions about the significance of mesophyll resistance during water stress.
The aim of the study was to identify the microbes which reach the cut surface of Norway spruce (Picea abies (L.) Karst.) stumps during the first year after felling by means of air born spores, determine their occurrence frequency and the combinations in which they occur, investigate the colour changes in the wood caused by microbes and identify the microbial species isolated from the sap- and heart-wood.
The material consisted of 360 spruce stumps. 300 of the stumps were innoculated with five different fungi (Phlebia gigantea, Botrytis cinerea, Gliocladium deliquescens, Trichoderma viride, Verticicladiella procera) in order to inhibit air-born attack by Heterobasidion annosum. 60 stumps were left untreated as controls.
The cultural characteristics of the following fungi isolated from the stumps have been described e.g.: Ceraceomerulius serpens, Chondrostereum purpureum, Cylindrobasidium evolvens, Peniophora pithya, Phlebia gigantea (Phlebiopsis gigantea) , P. subserialis, Sistotrema brinhmannii, Bjerkandera adusta, Coriolellus serialis, Trametes zonata, Armillariella mellea, Panellus mitis, Nectria fucheliana (microconidial-stage), Ascocoryne cylichnium (conidial-stage), Leptographium lundbergii, Acremonium butyri, Gliocladium deliquescens, Verticicladiella procera.
The proportion of Basidiomycotina fungi out of the whole material was 53 %, Ascomycotina and Deuteromycotina fungi 37,6 % and bacteria 7,3 %.
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The paper is a continuation of an earlier report by the author on the same subject (Acta Forestalia Fennica 133, 1973). Norway spruce (Picea abies (L.) H. Karst.) wounds were inoculated with Peniophora gigantea (Phlebiopsis gigantea) and the discolorations starting from the wounds were investigated three years after the wounding. Fomes annosus (Heterobasidion annosum) had infected 17 % of the total number of wounded trees. If no microbes were growing at the furthest point of the discoloration that had started from the wound, the discoloration advanced upward from wounds made at breast height at a rate of 61 cm/year in the dominant and 36 cm/year in the suppressed trees. In the dominant trees, a year after the wound was inflicted the discoloration had advanced at a rate of 50 cm/year and after three years the rate was 61 cm/year. This difference is not significant. Where microbes were present at the furthest point of discoloration, the discoloration had advanced 27 cm/year in one year and 42 cm/year in three years. Also, this difference is not significant.
A microbe was isolated from the furthest point of discoloration in only 13 out of 42 possible cases. The most common microbe was Stereum sanguinolentum. Bacteria showed the fastest rate of advance.
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The purpose of this study was that of providing a long-term timber production model (Kilkki and Pökkälä 1975) with growing stock models. The paper is divided into two parts; the first is concerned with generation of the stand data through Monte-Carlo simulation. The growing stock of each stand was described by a DBH-height distribution. The necessary information on the relationships between the stand characteristics was derived from sample plots measured in the national forest inventory of Finland. A total of 1,500 Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) H. Karst), and birch (Betula sp.) stands, each comprising 100 trees were provided by simulation.
In the second part, models predicting the form factor, timber assortment distribution, and value of the growing stock were derived through regression analysis for each species of tree. The predicting variables included the form factor of the basal area median tree, basal area median diameter, and height in the form factor models. In the timber assortment and value models, the only predicting variable was the volume of the basal area median tree. The Matchcurve-technique (Jensen 1973) was employed in derivation of the regression models.
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Water extracts of six common soil lichens, Cladonia alpestris, C. rangiferina, C. arbuscula (sylvatica), C. pleurota, Cetraria islandica, Stereocaulon paschale, inhibited growth of ectomycorrhizae of Pinus sylvestris (L.). Of 17 fungi (12 mycorrhizal) tested, many were inhibited while others were scarcely influenced or even occasionally stimulated by the extracts. Cladonia alpestris extract inhibited most fungi while C. rangiferina showed much less influence.
In pure culture synthesis experiments, 32P uptake of Pinus sylvestris was significantly reduced by C. alpestris extract. Different species of fungi showed widely variant abilities to pick up 32 P. in nursery experiments, much more vigorous growth of P. sylvestris and Picea abies (L.) H. Karst. was obtained on plots without C. alpestris than on paired plots covered with it. Betula verrucosa (B. pendula Roth) showed no difference. Under natural forest conditions, P. sylvestris seedlings grow much more rapidly where C. alpestris had been eliminated by road building or reindeer grazing than do seedlings only one meter distant under undisturbed C. alpestris cover. It is suggested that by properly controlled reindeer grazing, establishment and early growth of P. sylvestris on Cladonia sites can be much enhanced. By the time that C. alpestris could become re-established the pine seedlings would have grown large enough to suffer little from reindeer grazing. This study shows the continuity of the major components of the forest tundra biome – the dependence of pines, mycorrhizae, lichens, and reindeer and their predators (human or otherwise) upon each other for a healthy existence.
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In 1972, all Norway spruce (Picea abies (L.) H. Karst.) trees of a minimum 7 cm diameter at breast height growing in the sample plots of the Sixth National Forest Inventory were examined on the main island of Aland, Finland. The soundness of standing trees was estimated by means of external characteristics and increment borer chips. The trees were then felled and measured. They were cut into lengths, and the type and extent of decay were studied.
30% of the trees examined was affected by butt rot, ca. 3% by wound decay. A comparison of the results with those of the Sixth National Forest Inventory justifies the estimate that in Aland 23% of spruce trees exceeding 7 cm in diameter at 1.3 m had butt rot.
The proportion of decayed trees in the cubic volume was 31%. Decayed wood material accounted for 5% of the volume including bark. Butt rot increased towards the mature stands. The reduction in the number of timber trees due to decay was 14.5%, in their volume 21.5%, and in the volume of sulphite pulpwood 12%. The share of sulphate pulpwood increased from 1 to 10%. The total reduction in usable wood was 6.3%. The stumpage price of the trees fell by 10.3%. As the degree of decay increased the increment percentage of the trees decreased. The most common cause of butt rot was Fomes annosus (Heterobasidion annosum) found in 46% of the number of decayed trees. Armillaria mellea was found in 16%. Bacteria were found in 50% of the decayed trees.
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The purpose of the present study was to investigate the success of infecting Norway spruce (Picea abies) wounds with a mycelial suspension of Peniophora gigantea (now Phlebiopsis gigantea). In an approximately 100-year old spruce stand on Myrtillus type soil in Southern Finland, two dominant and two suppressed spruce trees were wounded each month during one year, and infected with P. gigantea. Control trees were only wounded. One year after wounding the trees were sawn into discs near the wound. Samples of the discs were cultured to identify the microbes.
In the suppressed trees, the P. Gigantea infection had been successful in 75 % of the wounds extending into heartwood. For dominant trees, the percentage was 50. In sapwood wounds the infection was considerably less successful. In two wounds of the control trees were noted airborne P. gigantea infection, and in four Fomes annosus (now Heterobasidion annosum).
Discoloration starting from the wounds was not a reliable proof that microbes were present. According to the variance analysis, the upward advance of discoloration without microbes showed a greater correlation with the crown class than with the type and site of the wounds. The downward advance depended more on the type of the wounds than the crown class.
A total of 37 fungi were identified by species or family, from the damaged trees. A large number of bacteria were also found. The most common fungi were the Penicillium species, and they had most often advanced farthest above and below the wound. Of the actual decay fungi, Stereum sanguinolentum showed the highest incidence and fastest growth. Coryne cylichnium and Cephalosporium species were also relatively common.
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The incidence of the conidiophores of Fomes annosus (Heterobasision annosum) was investigated in Helsinki in 1967–71 in a Norway spruce (Picea abies (L.) H. Karst.) stand growing on a site of Oxalis-Myrtillus type. The investigation comprised stump surfaces of spruce and pieces of wood, decayed by F. annosus, placed on the ground.
Conidiophores and conidia were seen during a few weeks in May-June on the surfaces of stumps covered by spruce branches. Conidiophores were sometimes seen on the stump surfaces even later in the summer and autumn, but by that time they were only very few. Their occurrence on the stumps that had not been covered was extremely rare, and the conidiophores were always very few in number. Surfaces of trees felled the year before showed no conidiophores. Conidiophores were also found below the pieces of decayed wood lying on the ground.
When spruce trees decayed by F. Annosus were felled in the summer and autumn, the surfaces of stumps covered with spruce branches showed the first conidiophores one week after the felling. The occurrence continued almost uninterruptedly until the winter.
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The present study is an attempt to establish the response to drainage of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) on some peatland sites, and to determine the revival of the trees and continuance of the growth after drainage. Growth of trees in four types of peatland types of drained peatlands drained between 1908-1918 were studied, and the results were compared with corresponding mineral soil sites
In pine the response to drainage was faster than in spruce in all age classes. Even the oldest groups of trees showed as good growth as trees of the same size growing on mineral soils. The rapidity of revival and the radial growth maximum are affected by the age of the tree at the time of ditching and the site fertility. The size of the trees, too, is of importance for the magnitude of post-drainage radial growth; the influence is similar in different sites. The basal area growth of trees growing on peat usually showed an unbroken increase during the entire post-drainage period. Neither the height growth indicates a decline in growth over time.
In the light of the results from sample tree analysis, it seems that tree growth gradually rises even after the revival period in peatlands originally covered by forest. The are some errors in the comparisons made, but it can be observed that aging of drainage areas as such does not mean that growth conditions become poorer.
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The influence of various environmental factors on the diameter growth of trees has been studied based on data collected by following daily increment of trees and various environmental factors during the growing season in 1964–1967. The field work was carried out in two experimental stands, a Scots pine (Pinus sylvestris L.) stand and a mixed stands growing birch (Betula sp.), Norway spruce (Picea abies (L.) H. Karst.) and Scots pine, in Southern Finland.
The results show that the temperature sums preceding the beginning of diameter growth were of the same magnitude in the years studied, which indicates dependence in the relationship. Formation of new xylem cells took place in the pine stem ca. every third day when the diameter growth was most active. No summer growth inhibition was detected in diameter growth.
None of the cumulative temperature sums tried determined the time of cessation of diameter growth. In several cases, positive correlation was found between the length of the growing season and the width of the annual ring formed. When studying the relationships between the diameter increment and the environmental factors, it was found that diameter increment was totally masked in the records by the hydrostatic changes in the stem. Relationships between the diameter increment and the environmental factors of the second day preceding growth were found to be poor. In studying the deviations of the recorded daily increments from the regression surface, no clear general trend was seen for pine and spruce, but clear diminishing trend toward the end og the growing season could be seen for birch in 1967.
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.
Disturbances caused by the European spruce bark beetle (SBB; Ips typographus L.) on Norway spruce (Picea abies (L.) H. Karst.), have increased immensely across Central and Northern Europe, and are expected to increase further as a result of climate change. While this trend has been noted in Finland, so far limited research has been published. To support proper SBB risk management in Finland, we compared stand properties between salvage loggings due to SBB damage during 2012–2020 (4691 cases) and spruce stands free of SBB damage. Also, we explored the role of landscape attributes as drivers of SBB damage. We considered the forest stand attributes of site fertility class, stand development class, soil type, stand mean diameter at breast height and mean stand age. Considered forest landscape attributes were the distance from SBB-damaged stands to the closest clear-cut, to previous-year SBB-damaged stands and to the previous-year wind-damaged stand. We used nationwide forest logging and forest stock data, and analysed forest stand attributes using chi-squared and Mann-Whitney U tests and landscape attributes using generalised linear mixed models. Based on our findings, the SBB didn’t damage stands randomly, but prevailed in mature stands (high age and high mean diameter at breast height), in herb-rich heath forest site types and in semi-coarse or coarse heath forest soil soils. We found correlation between the landscape variables and the number of salvage loggings, with a higher number of loggings due to SBB damage close to clear-cuts. Our results help to find risk areas of SBB damage.
We developed tree level biomass (dry weight) models for Norway spruce (Picea abies [L.] H. Karst.), silver birch (Betula pendula Roth), rowan (Sorbus aucuparia L.) and aspen (Populus tremula L.) growing in young spruce dominated seedling stands with high mixture of broadleaves. The study material was collected from three planted Norway spruce seedling stands located on mineral soil in southern Finland. Biomass models were estimated by individual tree component (stem, living branches, foliage, stump, and roots with diameter of 2 mm) by using a multi-response approach (seemingly unrelated regression), which estimated the parameters of the sub-models (tree component) simultaneously. Even though the application and generalization of the developed models can be restricted by the limited material, they provide new information of seedling biomass allocation and more reliable biomass predictions for spruce and birch growing in young seedling stand compared with those of the commonly applied biomass models (Repola 2008, 2009) in Finland. Repola’s models (2008, 2009) tended to produce biased predictions for crown and below-ground biomasses of seedlings by allocating too much biomass to roots and too little to needle and branches. In addition, this study provides biomass models for aspen and rowan, which were not previously available.
After a decades-long increasing trend, the recent results of the National Forest Inventory (NFI) reported a decline of forest growth in North Finland. The aim of this study was to assess climatic and reproduction influences behind the growth decline. We used tree-ring data that had been collected by NFI using systematic sampling. The tree-ring width series were detrended using the regional curve standardisation (RCS) removing age-related trends. The resulting tree-ring indices of Scots pine (Pinus sylvestris L.) showed decadal variations with low increment in the 1990s, and high increment in the 1980s and the early years of the current century. Thereafter, a prolonged growth reduction for pine started both on the mineral soil sites and peatlands. The tree-ring indices of Norway spruce (Picea abies (L.) Karst.) had less pronounced decadal variations and no trend-like reduction over the last 15 years. High spring and summer temperatures were found to enhance radial growth, but high winter temperatures were related to low growth for pine and spruce in the following summer. Temperature variation, accompanied by variables indicating years of drought and intensive flowering, accounted for 34% annual growth variance of pine and 21–44% for spruce. Thus, the results imply that climatic factors may have to some extent contributed to the recent growth reduction of pine. Due to its ecological and economic consequences growth decline needs to be further monitored and investigated. Moreover, analyses of stand and age structure, potentially affecting the growth decline, were beyond the scope of this paper, but also warrant further investigation.
Models that predict forest development are essential for sustainable forest management. Constructing growth models via regression analysis or fitting a family of sigmoid equations to construct compatible growth and yield models are two ways these models can be developed. In this study, four species-specific models were developed and compared. A compatible growth and yield stand basal area model and a five-year stand basal area growth model were developed for Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.). The models were developed using data from permanent inventory plots from the Swedish national forest inventory and long-term experiments. The species-specific models were compared, using independent data from long-term experiments, with a stand basal area growth model currently used in the Swedish forest planning system Heureka (Elfving model). All new models had a good, relatively unbiased fit. There were no apparent differences between the models in their ability to predict basal area development, except for the slightly worse predictions for the Norway spruce growth model. The lack of difference in the model comparison showed that despite the simplicity of the compatible growth and yield models, these models could be recommended, especially when data availability is limited. Also, despite using more and newer data for model development in this study, the currently used Elfving model was equally good at predicting basal area. The lack of model difference indicate that future studies should instead focus on model development for heterogeneous forests which are common but lack in growth and yield modelling research.
Pathogenic wood decay fungi such as species of Heterobasidion are some of the most serious forest pathogens in Europe, causing rot of tree boles and loss of growth, with estimated economic losses of eight hundred million euros per year. In conifers with low resinous heartwood such as species of Picea and Abies, these fungi are commonly confined to heartwood and thus external infection signs on the bark or foliage of trees are normally absent. Consequently, determining the extent of disease presence in a forest stand with field surveys is not practical for guiding forest management decisions such as optimal rotation time. Remote sensing technologies such as airborne laser scanning and aerial imagery are already used to reduce the reliance on fieldwork in forest inventories. This study aimed to use remote sensing to detect rot in spruce (Picea abies L. Karst.) forests in Norway. An airborne hyperspectral imager provided information for classifying the presence or absence of rot in a single-tree-based framework. Ground reference data showing the presence of rot were collected by harvest machine operators during the harvest of forest stands. Random forest and support vector machine algorithms were used to classify the presence and absence of rot. Results indicate a 64% overall classification accuracy for presence-absence classification of rot, although additional work remains to make the classifications usable for practical forest management.
Thekopsora areolata (Fr.) Magnus is a serious cone pathogen that reduces seed crop of Picea abies (L.) Karst. and other Picea spp. Natural sporulation of T. areolata was investigated in nine Norway spruce seed orchards suffering from severe successive T. areolata epidemics in Finland. Habitats occupied by Vaccinium myrtillus L., V. vitis-idaea L., Empetrum nigrum L. and Calluna vulgaris (L.) Hull, and a number of other wild species belonging to ground flora were investigated for Thekopsora areolata uredinia 9–10 times in May–September 2018–2019. Occurrence of Thekopsora uredinia was estimated in current-year leaves of the plants in ca. 25 sample plots of 1 m2 in each seed orchard. A sample of plant leaves with rust uredinia or necrotic pustules were collected from each plot. No rust fruiting stages of T. areolata were found on any of the test species of ground flora. However, rust uredinia were observed regularly on leaves of V. myrtillus and V. vitis-idaea in all seed orchards between mid-July and the end of September. Rust sporulation started on V. myrtillus in July and on V. vitis-idaea in August. Based on symptoms, uredinia and spore morphology, the rust on both V. myrtillus and V. vitis-idaea was identified as blueberry rust, Naohidemyces vaccinii (Jørst.) S. Sato, Katsuya & Y. Hirats. ex Vanderwegen & Fraiture. The uredinial stage of the rust on Vaccinium spp. were described. No evidence of natural sporulation of T. areolata on wild plant species other than Prunus was observed in Finnish Norway spruce seed orchards.
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.
Forests and forestry will encounter several changes of unknown magnitude within the coming decades. In the Nordic, long rotations complicate any anticipation to the upcoming changes. Tree breeding can contribute to coping with these changes. The time span of implementing breeding results in practice may be shortened through vegetative propagation. Introducing vegetative propagation to forest regeneration may phase several challenges before adopted by the industry, some of which are related to perceptions about new technology. Firstly, private forest owners are in a key role in implementing the technology in practice; although they do not represent the overall public, they are the decision makers in their own estates regarding forestry and forest regeneration. Secondly, the professionals related to the production of forest regeneration material and plants from forest species are in a key role when it comes to practically introducing the new technology to the forest owners. In this survey, perceptions of forest owners and professionals towards tree breeding and vegetative propagation were investigated. Additionally, the respondents were asked which traits they considered important to be improved by breeding, and their willingness to pay for these improved traits. The respondents valued the most: improved pest and pathogen resistance, improved resilience of forest in changing climate, and securing the species’ gene pool. Responses indicated that forest owners would be willing to pay more for the improved traits in forest regeneration material. The current novel study provides a foundation to concern public awareness regarding tree breeding and vegetative propagation in the future.
The alternate host range of cherry-spruce rust is poorly studied although such information could be important in protecting spruce seed orchards from infections. Pathogenicity of cherry-spruce rust, Thekopsora areolata (Fr.) Magnus, was investigated on potential alternate host species in a greenhouse and in a laboratory in Finland. Five common species of Ericaceae, Vaccinium myrtillus L., V. uliginosum L., V. vitis-idaea L., Empetrum nigrum L. and Arctostaphylos uva-ursi (L.) Spreng, were inoculated in the greenhouse using aeciospores from seven Norway spruce [Picea abies (L.) H. Karst.] seed orchards suffering from T. areolata in 2018. In addition, young detached leaves of Vaccinium spp. and 17 other plant species of ground vegetation from eight Norway spruce seed orchards were inoculated with aeciospores from six seed orchards in the laboratory in 2019. Also, young leaves of Prunus padus L. trees growing within the seed orchards or close to them were inoculated as controls. None of the inoculated leaves of the potential alternate hosts formed uredinia either in the greenhouse or in the laboratory. In contrast, leaves of P. padus from the seed orchards were infected by the six spore sources from six seed orchards and produced uredinia. As T. areolata spores were able to infect only P. padus, but not the other tested species belonging to ground flora, it was concluded that T. areolata disperses only via Prunus spp. in Finnish seed orchards.
Cherry-spruce rust caused by Thekopsora areolata (Fr.) Magnus is a serious cone pathogen of Norway spruce [Picea abies (L.) Karst.]. The rust causes great economical losses in seed orchards specialized in the production of high quality seeds. Germination range of T. areolata aeciospores from rust populations (spore sources) in seven Finnish Norway spruce seed orchards was tested on water agar and malt agar at nine temperatures varying between 6–30 °C. The temperature range of spore germination was high varying between 6 °C and 27 °C, while germination was retarded at 30 °C. The peak in germination rate of all spore sources occurred between 15–24 °C. In a model with fixed effects of agar media, temperature and spore source, temperature had the most significant effect on germination. Spore source had a less significant effect, while agar media had a non-significant effect on germination. The rust was able to germinate at low temperatures corresponding to temperatures when the thermal growing season starts at 5 °C in the spring. As spores from cones from both the spruce canopy and the ground showed very similar germination ranges, it indicated the great capacity of all spores of the rust to germinate early in the spring. Hot temperatures with over 30 °C drastically reduced germination of the rust.
In Nordic countries, tree planting of seedlings is mainly performed during spring and early summer. Interest has increased in extending the planting window throughout the unfrozen growing season. This study compared the success of one-year-old spring, summer and autumn plantings in practical forestry in Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) in southern and central Finland. Planting success was based on the number of viable seedlings per hectare relative to a species-specific target density. The influence of different factors to poor planting results were determined, including quality of site preparation and planting, and sources of natural damage. Overall, in Norway spruce, 85, 69 and 84% and in Scots pine 53, 55 and 40% of spring, summer and autumn plantings succeeded. In Norway spruce, the planting results were consistent between the southern and central regions, whereas in Scots pine, the success was slightly lower in the south. The poor work quality and a low density of appropriate planting spots, contributed to poor planting results, regardless of planting season, region or tree species. Considering different damages, especially mammal damage contributed to the failure of Scots pine spring plantings, whereas in summer plantings, corresponding single failure reason could not be identified. Based on our findings, extending the planting season of Norway spruce could be recommended in both regions. For Scots pine, there is still significant uncertainty about the success of summer and autumn plantings, partially due to the limited number of plantings available for analyses.
Based on data from long-term experimental fields with Norway spruce (Picea abies (L.) H. Karst.), we developed new stem taper and bark functions for Norway. Data was collected from 477 trees in stands across Norway. Three candidate functions which have shown good performance in previous studies (Kozak 02, Kozak 97 and Bi) were fitted to the data as fixed-effects models. The function with the smallest Akaike Information Criterion (AIC) was then chosen for additional analyses, fitting 1) site index-dependent and 2) age-dependent versions of the model, and 3) fitting a mixed-effects model with tree-specific random parameters. Kozak 97 was found to be the function with the smallest AIC, but all three tested taper functions resulted in fairly similar predictions of stem taper. The site index-dependent function reduced AIC and residual standard error and showed that the effect of site index on stem taper is different in small and large trees. The predictions of the age-independent and age-dependent models were very close to each other. Adding tree-specific random parameters to the model clearly reduced AIC and residual variation. However, the results suggest that the mixed-effects model should be used only when it is possible to calibrate it for each tree, otherwise the fixed-effects Kozak 97 model should be used. A model for double bark thickness was also fitted as fixed-effects Kozak 97 model. The model behaved logically, predicting larger relative but smaller absolute bark thickness for small trees.
Progenies from open pollinated cones collected in natural populations of Norway spruce (Picea abies (L.) Karst.) distributed along two altitudinal transects in Mid-Norway were tested in the nursery, in short term tests and in long-term field trials. The populations showed clinal variation related to the mean annual temperatures of the populations, with the earliest bud flush and cessation of shoot elongation and lowest height at age nine years for the high altitude populations. Within population variation was considerable as the narrow sense heritability for these traits was 0.67, 0.31 and 0.09 in one transect and 0.55, 0.18 and 0.14 in the other transect, respectively. Lammas shoots occurred in the short term trials with large variation in frequency between years. There was significant family variation for this trait, but also interactions between populations and year. The variance within populations was considerably larger in the populations from low altitude compared to the high-altitude populations. Significant genetic correlations between height and phenology traits and damage scores indicate that families flushing early and ceasing growth late were taller. Taller families also had higher frequencies of damages. Selection of the top 20% families for height growth in short term tests at age nine years gave a simulated gain of 11% increased height growth at age 18 years in long term trials at altitudes similar to those of origin of the populations. The gain was negative when high altitude populations were selected based on testing in the lowland.
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.
The mean temperature during the potential growing season (April–September) may increase by 1 °C by 2030, and by 4 °C, or even more, by 2100, accompanied by an increase in atmospheric CO2 concentrations of 536–807 ppm, compared to the current climate of 1981–2010, in which atmospheric CO2 is at about 350 ppm. This may affect both the growth and frost hardiness of boreal trees. In this work, we studied the responses of height and autumn frost hardiness development in 22 half-sib genotypes of one-year-old Norway spruce (Picea abies (L.) Karst.) seedlings to elevated temperatures and atmospheric CO2 concentration under greenhouse conditions. The three climate treatments used were: T+1 °C above ambient and ambient CO2; T+4 °C above ambient and ambient CO2; and T+4 °C above ambient and elevated CO2 (700 ppm). The height growth rate and final height were both higher under T+4 °C compared to T+1 °C. Temperature increase also delayed the onset, and shortened the duration, of autumn frost hardiness development. Elevated CO2 did not affect the development of height or frost hardiness, when compared to the results without CO2 elevation under the same temperature treatment. Higher temperatures resulted in greater variation in height and frost hardiness development among genotypes. Three genotypes with different genetic backgrounds showed superior height growth, regardless of climate treatment; however, none showed a superior development of autumn frost hardiness. In future studies, clonal or full-sib genetic material should be used to study the details of autumn frost hardiness development among different genotypes.
Adult pine weevils (Hylobius abietis (L.)) feed on the tender bark of branches and roots of mature conifer trees and on the stem bark of conifer seedlings. Their feeding on mature trees does not cause any economic damage, but their feeding on planted seedlings is so devastating that the pine weevil is considered one of the most important forest pest insects in Europe. We asked whether the pine weevil prefers seedlings over other regularly utilized food sources. This question is of particular interest because new approaches to seedling protection are based on decreasing any preference for seedlings by using less palatable plants or by enhancing their defence (by genetic selection or by methyl jasmonate treatment). In a laboratory choice experiment we tested pine weevil feeding preferences for seedlings compared with branches and roots from mature trees (separately for Norway spruce and Scots pine). Pine weevils preferred roots, but not branches, of Norway spruce over seedlings of the same species. With Scots pine there were no clear preferences, but the weevils showed a tendency to prefer roots over seedlings. These results provide support for seedling protection approaches that attempt to redirect pine feeding from planted seedlings to other food sources.
Genetically improved Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) are extensively used in operational Swedish forestry plantations. However, relatively little is known about the stem slenderness (height-diameter ratio) of genetically improved material. Thus, in this study we investigated effects of plus-tree selection on stem slenderness of Norway spruce and Scots pine in Sweden by evaluating both the plus-tree selection and a large number of progeny trials. Species-specific models for predicting the height-diameter ratio were estimated using regression and mixed model approach. Our results show that phenotypic plus-tree selection promoted less slender Norway spruce trees and more slender Scots pine trees compared to neighboring trees. Similar results were also found for the progeny trials which indicated that genetics played a prominent role in the phenotypic appearance. Compared to the progeny of neighboring trees, Norway spruce plus-tree progenies had a 5.3% lower height-diameter ratio, while Scots pine plus-tree progenies had a 1.5% greater height-diameter ratio. The narrow sense heritability for height-diameter ratio was 0.19 for Norway spruce and 0.11 for Scots pine, indicating that it is possible to modify the height-diameter ratio by breeding. Correlation coefficients between breeding values for height-diameter ratio and diameter were negative for Scots pine (–0.71) and Norway spruce (–0.85), indicating that selection for diameter only would result in less slender stems of both species. Similar correlations were also found between breeding values for height-diameter ratio and height of Scots pine (–0.34) and Norway spruce (–0.74).
Short day (SD) treatment is used as a dormancy induction in forest tree seedling nurseries in the boreal forest zone. However, SD treatment has caused early bud burst in the following spring, which may expose the seedlings to spring frosts. Because the mechanisms affecting earlier bud burst in SD treated seedlings are not fully understood yet, here we have studied the effect of SD treatment on the structure of buds in Norway spruce [Picea abies (L.) Karst.] seedlings. Seedlings were exposed to SD treatments or natural (CTRL) light and photoperiod in July in a nursery in Central Finland. The experiments included two lots of seedlings over two summers and the analyses were done under a stereo microscope. SD treatment advanced initiation of bud scales and formation of needle primordia, and thus the formation period was shorter in CTRL seedlings. In mature buds, no differences in primordial shoots were found between the treatments, whereas notable differences were found in bud scales. The SD buds had fewer and shorter bud scales than the CTRL buds. This led to significantly shorter bud scale complex and, consequently, to shorter buds in SD than in CTRL seedlings. Buds and needles matured earlier in SD treated seedlings. In the following spring, the primordial shoots started to elongate in both treatments around mid-May, when the SD buds started to break down, whereas CTRL buds started to break down in late May. The fewer number and shorter height of protective bud scales may expose buds to harsh winter temperatures and early loss of scales may predispose the SD buds to spring frosts.
The reach of different tree species’ crowns and the velocity of gap closure during the occupation of canopy gaps resulting from mortality and thinning during stand development determine species-specific competition and productivity within forest stands. However, classical dendrometric methods are rather inaccurate or even incapable of time- and cost-effectively measuring 3D tree structure, crown dynamics and space occupation non-destructively. Therefore, we applied terrestrial laser scanning (TLS) in order to measure the structural dynamics at tree and stand level from gap cutting in 2006 until 2012 in pure and mixed stands of Norway spruce (Picea abies [L.] Karst.) and European beech (Fagus sylvatica L.). In conclusion, our results suggest that Norway spruce invests newly available above-ground resources primarily into DBH as well as biomass growth and indicate a stronger resilience against loss of crown mass induced by mechanical damage. European beech showed a vastly different reaction, investing gains from additional above-ground resources primarily into faster occupation of canopy space. Whether our sample trees were located in pure or mixed groups around the gaps had no significant impact on their behavior during the years after gap cutting.
Crown dimensions are correlated to growth of other parts of a tree and often used as predictors in growth models. The crown-to-bole diameter ratio (CDBDR), which is a ratio of maximum crown width to diameter at breast height (DBH), was modelled using data from permanent sample plots located on Norway spruce (Picea abies (L.) Karst.) and European beech (Fagus sylvatica L.) stands in different parts of the Czech Republic. Among various tree and stand-level measures evaluated, DBH, height to crown base (HCB), dominant height (HDOM), basal area of trees larger in diameter than a subject tree (BAL), basal area proportion of the species of interest (BAPOR), and Hegyi’s competition index (CI) were found to be significant predictors in the CDBDR model. Random effects were included using the mixed-effects modelling to describe sample plot-level variation. For each species, the mixed-effects model described a larger part of the variation of the CDBDR than nonlinear ordinary least squares model with no trend in the residuals. The spatially explicit mixed-effects model showed more attractive fit statistics [conditional R2 ≈ 0.73 (spruce), 0.78 (beech)] than its spatially inexplicit counterpart [conditional R2 ≈ 0.71 (spruce), 0.76 (beech)]. The model showed that CDBDR increased with increasing HDOM – a measure that combines the stand development stage and site quality – but decreased with increasing HCB and competition (increasing BAL and CI), and decreasing proportions of the species of interest (increasing BAPOR). For both species, the spatially explicit mixed-effects model should be a preferred choice for a precise prediction of the CDBDR. The CDBDR model will have various management implications such as determination of spacing, stand basal area, stocking, and planning of appropriate species mixture.
Genetically improved Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) are used extensively in operational Swedish forestry plantations to increase production. Depending on the genetic status of the plant material, the current estimated genetic gain in growth is in the range 10–20% for these species and this is expected to increase further in the near future. However, growth models derived solely from data relating to genetically improved material in Sweden are still lacking. In this study we investigated whether an individual tree growth model based on data from unimproved material could be used to predict the height increment in young trials of genetically improved Norway spruce and Scots pine. Data from 11 genetic experiments with large genetic variation, ranging from offspring of plus-trees selected in the late 1940s to highly improved clonal materials selected from well performing provenances were used. The data set included initial heights at the age of 7–15 years and 5-year increments for almost 2000 genetic entries and more than 20 000 trees. The evaluation indicated that the model based on unimproved trees predicted height development relatively well for genetically improved Norway spruce and there was no need to incorporate a genetic component. However, for Scots pine, the model needed to be modified. A genetic component was developed based on the genetic difference recorded within each trial, using mixed linear models and methods from quantitative genetics. By incorporating the genetic component, the prediction errors were significantly reduced for Scots pine. This study provides the first step to incorporate genetic gains into Swedish growth models and forest management planning systems.
The ongoing climate change may have a distinct effect on Norway spruce growth, one of the most important tree species in European forest management. Therefore, the understanding and assessment of climate-growth relationship can help to reveal relevant patterns in temporal variability that may result in lower tree vitality and decline. The main objective of our study was to evaluate the long-term climate-growth variability of Norway spruce in south-eastern Norway, at the northern edge of the temperate zone. We sampled in total 270 dominant and co-dominant trees from 18 plots in south-eastern Norway. We analysed stem cores and evaluated crown condition parameters to assess the retrospective tree growth and vitality. Despite considerable differences in the crown parameters, high similarity among tree-ring width (TRW) series allowed compiling the regional tree-ring width chronology. Correlations between TRW and climate parameters showed temporal instability in their relationship during the period 1915–2012. While we did not detect any significant relationships between TRW and climate parameters in the first half of the study period (1915–1963), a significant correlation between TRW and spring precipitation was observed for the period 1964–2012. This shift appeared concurrent with temperatures reaching above-average values compared to the average of the climate normal period 1961–1990.
Stump wood is a possible alternative to fossil fuel. Its harvesting, however, disturbs the ground and this has not yet been quantified at stump level. Such disturbance is likely to be dependent on stump size, type of soil and timing of stump harvesting. Therefore, we measured ground disturbance and root breakage diameter at two Norway spruce sites with sandy glacial till soil. The sites were harvested with a fork type head, 6 and 18 months after clear cutting. Measurements were made within 2 weeks of harvest. No difference was found between the two sites. The mean area of disturbed ground was 6.06 (std 3.14) m2 per stump and increased exponentially with stump size. A regression function modelling the relationship was constructed. Unexpectedly, many fine roots where extracted in the harvest. The arithmetic and basal area weighted mean root breakage diameter was 4.6 (std 2.2) and 29.5 (std 17.9) mm, respectively. There seems to be a limited increase in root breakage diameter with increased stump size. The small root breakage diameter is associated with reduced fuel quality and greater nutrient removal. It appears that much of the ground disturbance is associated with the creation of ruts rather than stump harvest per se. Stump harvesting disturbs a larger percentage of the area of a harvested site than mounding. Postponing stump harvest by one year did not decrease the ground disturbance or increase the root breakage diameter. To achieve less disturbance and larger root breakage diameter, probably new stump harvesting technology is required.
The boreal timber- and tree-line forests grow in harsh environmental conditions in their outermost distribution limit. Here even small environmental changes may cause dramatic changes in the distribution of tree species. We examined changes of the forest lines of Norway spruce (Picea abies (L.) H. Karst.) and Scots pine (Pinus sylvestris L.) in Finnish Lapland five times during 1983–2009. We monitored the number of stems and the volume of the growing stock in thirteen different locations in forest-line areas. The linear temporal trends and the variations of these response variables were used as indicators of a possible change during the study period. Spruce showed a significant increase both in the volume of the growing stock (up to 40% increase) and in the total stem number (up to 100% increase). A significant increase in the volume of the growing stock was observed in the pine data as well (up to 70% increase), whereas the stem number stagnated or even decreased. The results suggest that spruce needs favourable conditions to have an abundant regeneration, but after the establishment the seedlings seem to be more resistant against biotic and abiotic disturbances than pine seedlings. The increasing stand volume might result in a climate-related northward and upward extension of forests in the future. However, our results show that responses in the boreal forest line are species and location specific and a more favourable climate does not necessarily lead to an advance of the coniferous forest line.
The density of Picea abies [L.] Karst. regeneration on different microsites, the quantity and quality of woody microsites, and seedling occurrence probability on stumps and fallen deadwood were studied in a subalpine forest that has been under protection for approximately 30–40 years (Gorce Mountains in the western Carpathians). Thirty percent of seedlings and 29% of saplings grew on stumps and fallen deadwood, while the remaining regeneration occurred on soil surface and mounds created by uprooted trees. The occurrence probability of Picea seedlings on fallen deadwood increased with deadwood diameter and decay stage and with the volume of living trees, and decreased with increased density of living trees, sapling density, and land slope. Furthermore, seedlings were more likely to grow on stumps with a greater diameter and in plots with higher sapling density, but less likely to grow on higher stumps. Stumps and fallen deadwood covered about 4% of the forest floor, but the material that is most important for promoting regeneration (strongly decomposed logs and those of a diameter exceeding 30 cm) took up only about 22 m2 ha-1. We have concluded that in a subalpine forest that has been protected for 30–40 years regeneration processes take place mostly on soil surface and stumps. The role of fallen deadwood increases over time as a greater number of suitable logs (in terms of size and decay stage) become available.