Relationships between long-term trends of air temperature,precipitation, nitrogen nutrition and growth of coniferous stands in Central Europe and Finland

Height growth of 19 Scots pine (Pinus sylvestris) and Norway spruce (Picea abies) stands in Germany, Austria and Finland, for which long-term records of foliar nutrient levels were available, was assessed retrospectively by stem analyses and compared with data from regionally applied yield tables as references. Gridded historical time series of monthly temperature and precipitation were used to characterise the meteorologic conditions at the sampling sites. Climate parameters were tested against height growth in period 1950–2000, and needle N content was tested against height growth for the periods where N measurements were available by means of graphical comparison, as well as simple and multiple regression analyses with the aim to get evidence for causes of possible growth acceleration. Trends of referenced height increment of six out of nine Scots pine stands in Germany were positive during the observation period, and improved N nutrition appeared to be the most important driving factor for this growth acceleration. The variation of precipitation—exhibiting no consistent and uniform long-term temporal trend during the observation period—in contrast seems to be mainly responsible for the interannual fluctuation of height growth. We were not able to detect any general statistical influence of temperature parameters on height growth, although they generally increased. The referenced height growth of three Finnish pine stands slightly decreased during the observation period and there was no indication of a significant improvement of their N supply. Among four Norway spruce stands investigated in Germany and Austria, referenced height increment also increased in three cases; there was again some evidence that improved N nutrition was the stimulating factor. At three study sites in Finland, however, referenced height growth of this species decreased at least from 1985 onwards, whereas mostly no significant trends in N nutrition or precipitation were identified. These differences observed between species and regions are discussed in detail.     

Changes of soil chemistry,stand nutrition,and stand growth at two Scots pine (<Emphasis Type="Italic">Pinus sylvestris</Emphasis> L.) sites in Central Europe during 40 years after fertilization,liming, and lupine introduction

Long-term (40 years) effects of two soil amelioration techniques [NPKMgCa fertilization + liming; combination of PKMgCa fertilization, liming, tillage, and introduction of lupine (Lupinus polyphyllus L.)] on chemical topsoil properties, stand nutrition, and stand growth at two sites in Germany (Pfaffenwinkel, Pustert) with mature Scots pine (Pinus sylvestris L.) forest were investigated. Both sites are characterized by base-poor parent material, historic N and P depletion by intense litter-raking, and recent high atmospheric N input. Such sites contribute significantly to the forested area in Central Europe. Amelioration resulted in a long-term increase of pH, base saturation, and exchangeable Ca and Mg stocks in the topsoil. Moreover, significant losses of the forest floor in organic carbon (OC) and nitrogen stocks, and a decrease of the C/N ratio in the topsoil were noticed. The concentrations and stocks of OC and N in the mineral topsoil increased; however, the increases compensated only the N, but not the OC losses of the forest floor. During the recent 40 years, the N nutrition of the stands at the control plots improved considerably, whereas the foliar P, K, and Ca concentrations decreased. The 100-fascicle weights and foliar concentrations of N, P, Mg, and Ca were increased after both amelioration procedures throughout the entire 40-year period of investigation. For both stands, considerable growth acceleration during the recent 40 years was noticed on the control plots; the amelioration resulted in an additional significant long-term growth enhancement, with the NPKMgCa fertilization liming + being more effective than the combination of PKMgCa fertilization, liming, tillage, and introduction of lupine. The comprehensive evaluation of soil, foliage, and growth data revealed a key relevance of the N and P nutrition of the stands for their growth, and a change from initial N limitation to a limitation of other growth factors (P, Mg, Ca, and water).     

Fertilization Experiments on Forest Mineral Soils: A Review of the Norwegian Results

The paper gives a brief overview of the background, history and main results of forest fertilization experiments on mineral soils in Norway. Positive results of initial phosphorus (P) fertilization on survival and growth of Norway and Sitka spruce have only been achieved in the coastal districts of western Norway. Other elements have seldom given any significant effect. In young and old stands of Norway spruce and Scots pine nitrogen (N) fertilization with 150 kg N ha -1 usually gave increment increases in the range of 1-2 m 3 ha -1 yr -1 , for a period of 6-8 yrs after application. Given individually, no other element has proved stimulating to stem growth in a similar way. In young Norway spruce stands P has often given additional growth response when given together with N. Liming has been shown to have no or negative effects on tree growth. Fertilization experiments have changed from being management orientated towards addressing the problems of possible nutrient imbalances.     

Fine root morphological adaptations in Scots pine, Norway spruce and silver birch along a latitudinal gradient in boreal forests

Variability in short root morphology of the three main tree species of Europe's boreal forest (Norway spruce (Picea abies L. Karst.), Scots pine (Pinus sylvestris L.) and silver birch (Betula pendula Roth)) was investigated in four stands along a latitudinal gradient from northern Finland to southern Estonia. Silver birch and Scots pine were present in three stands and Norway spruce was present in all stands. For three fertile Norway spruce stands, fine root biomass and number of root tips per stand area or unit basal area were assessed from north to south. Principal component analysis indicated that short root morphology was significantly affected by tree species and site, which together explained 34.7% of the total variability. The range of variation in mean specific root area (SRA) was 51-74, 60-70 and 84-124 m(2) kg(-1) for Norway spruce, Scots pine and silver birch, respectively, and the corresponding ranges for specific root length were 37-47, 40-48 and 87-97 m g(-1). The range of variation in root tissue density of Norway spruce, Scots pine and silver birch was 113-182, 127-158 and 81-156 kg m(-3), respectively. Sensitivity of short root morphology to site conditions decreased in the order: Norway spruce > silver birch > Scots pine. Short root SRA increased with site fertility in all species. In Norway spruce, fine root biomass and number of root tips per m(2) decreased from north to south. The differences in morphological parameters among sites were significant but smaller than the site differences in fine root biomass and number of root tips.     

Growth response of coniferous stands to whole‐tree harvesting in early thinnings

A series of 15 field experiments was established to quantify the growth response of first‐thinning stands of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst) to whole‐tree harvesting and to estimate the need for nutrient compensation. The experiments were undertaken in Finland, Norway and Sweden and represent a wide range of site conditions. The site index (H ₁₀₀) of Scots pine stands varied from 19 to 29 m, and that of Norway spruce stands from 28 to 36 m. Total amounts of biomass and nutrients removed were calculated based on data obtained from felled sample trees. During the first 5‐yr period the growth response to the removal of logging residues varied considerably in both pine and spruce stands. Regression analyses did not reveal any functions that explained the variation in results satisfactorily. In cases where whole‐tree harvesting influenced tree growth negatively, this effect was counteracted by compensatory fertilization. It was concluded that to determine the response of remaining trees to harvesting intensity reliably, the post‐harvest period analysed must be longer than 5 yrs.     

Larval performances and life cycle completion of the Siberian moth, <Emphasis Type="Italic">Dendrolimus sibiricus</Emphasis> (Lepidoptera: Lasiocampidae), on potential host plants in Europe: a laboratory study on potted trees

The Siberian moth, Dendrolimus sibiricus, Tschtv. is the most harmful defoliator of coniferous forests in North Asia. The pest has already spread over the Urals and continues moving westwards. Recently, it has been recommended for quarantine in member countries by European and Mediterranean Plant Protection Organization (EPPO). The performances of the pest on coniferous species planted in Europe were assessed on a range of potted trees corresponding to the spectrum of economically important conifers in the EU: European larch Larix decidua, Norway spruce Picea abies, Scots pine Pinus sylvestris, European black pine Pinus nigra, and the North American species: Douglas fir Pseudotsuga menziesii and grand fir Abies grandis. Larvae showed a potential to survive and complete the development on all these host tree species. Favorable hosts were grand fir, European larch, and Douglas fir that allowed higher survival, better larval development, and as a result, yielded heavier pupae and adult moths with higher longevity. Black pine was a poor host but, however, could still support larval and pupal development. Norway spruce and Scots pine had an intermediate behavior. If accidentally introduced to Europe, the Siberian moth may become especially damaging in forest stands predominated by European larch and by the North American firs. Norway spruce and especially the two-needle pines will be less prone to intensive defoliation by this species. The fact that the pest may damage the range of economically important coniferous species should be taken into account in the pest risk assessment for Europe and also for North America where the Siberian moth occurrence is considered likely.     

Effect of uninucleate Rhizoctonia on Scots pine and Norway spruce seedlings

One‐year‐old container‐grown seedlings were planted in spring on clear cut areas: the Norway spruce (Picea abies) on a moist upland site (Myrtillus‐type) and Scots pine (Pinus sylvestris) on a dryish upland site (Vaccinium‐type). While still in the nursery, half of the seedlings of each species had been inoculated during the previous summer, with a uninucleate Rhizoctonia sp., a root dieback fungus. At outplanting all the seedlings appeared healthy and had a normal apical bud, although the height of the inoculated seedlings was less than that of the uninoculated control seedlings. At the end of the first growing season after planting, the mortality of inoculated Scots pine and Norway spruce seedlings was 25 and 69%, respectively. After two growing seasons the mortality of inoculated seedlings had increased to 38% for Scots pine and 93% for Norway spruce. The mortality of control seedlings after two growing seasons in the forest was 2% for Scots pine and 13% for Norway spruce. After outplanting the annual growth of inoculated seedlings was poor compared with the growth of control seedlings. These results show that, although Rhizoctonia‐affected seedlings are alive and green in the nursery, the disease subsequently affects both their survival and growth in the forest.     

Heterobasidion annosum root rot in Picea abies: Modelling economic outcomes of stump treatment in Scandinavian coniferous forests

Abstract

The economic outcomes of stump treatment against spore infections of the root rot pathogen Heterobasiodion annosum s. l. were analysed based on simulations in four stands typical of Swedish forestry and forest management: (A) Norway spruce [Picea abies (L.) Karst.] stand on former agricultural soil (SI?=?32), (B) Norway spruce stand (SI?=?26) on forest land; (C) Mixed stand of Norway spruce and Scots pine (Pinus sylvestris L.) (SI?=?24) with only H. parviporum present, i.e. no infection of Scots pine and no possibility of interspecies spread of disease between hosts; and (D) same as C, but H. annosum s. str. (Fr.) Bref and H. parviporum Niemelä & Korhonen present, i.e. interspecies spread of disease possible. Models for disease development, growth and yield and cross-cutting were used in the simulations. The simulated decay frequency in Norway spruce trees ranged between 2 and 90%. Stump treatment at the previous final felling and in all thinning operations was profitable at interest rates 1 and 3% in stands A, B and D, but not in stand C. In stand C, no stump treatment at all or treatment in thinnings only gave the highest net future value. Implications for stump treatment in practical forestry are discussed.     

Impacts of changing climate on the productivity of Norway spruce dominant stands with a mixture of Scots pine and birch in relation to water availability in southern and northern Finland

A process-based ecosystem model was used to assess the impacts of changing climate on net photosynthesis and total stem wood growth in relation to water availability in two unmanaged Norway spruce (Picea abies) dominant stands with a mixture of Scots pine (Pinus sylvestris) and birch (Betula sp.). The mixed stands were grown over a 100-year rotation (2000-99) in southern and northern Finland with initial species shares of 50, 25 and 25% for Norway spruce, Scots pine and birch, respectively. In addition, pure Norway spruce, Scots pine and birch stands were used as a comparison to identify whether species' response is different in mixed and pure stands. Soil type and moisture conditions (moderate drought) were expected to be the same at the beginning of the simulations irrespective of site location. Regardless of tree species, both annual net canopy photosynthesis (P(nc)) and total stem wood growth (V(s)) were, on average, lower on the southern site under the changing climate compared with the current climate (difference increasing toward the end of the rotation); the opposite was the case for the northern site. Regarding the stand water budget, evapotranspiration (E(T)) was higher under the changing climate regardless of site location. Transpiration and evaporation from the canopy affected water depletion the most. Norway spruce and birch accounted for most of the water depletion in mixed stands on both sites regardless of climatic condition. The annual soil water deficit (W(d)) was higher on the southern site under the changing climate. On the northern site, the situation was the opposite. According to our results, the growth of pure Norway spruce stands in southern Finland could be even lower than the growth of Norway spruce in mixed stands under the changing climate. The opposite was found for pure Scots pine and birch stands due to lower water depletion. This indicates that in the future the management should be properly adapted to climate change in order to sustain the productivity of mixed stands dominated by Norway spruce.     

From planting to 26 years of age – actual growth and estimated volume scenarios for spruces and pines

The objective of this study was to compare the survival and volume of conifer stands at 26 years of age with their status at planting. Survival, growth and damage were studied in eight clear felled stands regenerated in 1972. Five of the areas were planted with Norway spruce (Picea abies (L.) Karst.) and three with Scots pine (Pinus sylvestris L.). The plantings were examined in 1972 and 1974. In 1974, the number of living undamaged planted seedlings was low (10–15%). However, the number of undamaged seedlings was supplemented by naturally regenerated conifer and birch seedlings. The total number of undamaged seedling in 1974 was equivalent to 20–30% of the number of seedlings planted. In 1998, the main species in three stands had changed from Norway spruce to Scots pine, and in one stand from Norway spruce to birches. Actual volume in 1998 for the stands was compared to stand volume generate according to five scenarios based on recommended and actual seedling number in 1972 and 1974. The actual volume was 64% of that expected if the recommended number of trees had been planted. Naturally regenerated Scots pine and Norway spruce increased stand density in 1998. The actual volume was 37% higher than the average volume in the surrounding county. On average, 36% of the trees were damaged. More than 50% of the total damage was caused by moose (Alces alces L.). For Scots pine, moose or other browsing animals damaged 30% of the trees. The results of this study indicate that the 1998 volume was higher than expected, considering the low number of undamaged seedlings in 1974. This was mainly due to the large amount of naturally regenerated plants. In addition, the results indicate that the volume could have been higher if the initial conditions had been better. Despite the low number of undamaged seedlings in 1974, seven of the eight studied stands produced a higher volume than the average stand for the region. In practise, high numbers of seedlings should be planted on scarified areas. In most cases there will be a supply of naturally regenerated seedlings.     

Irradiance in young stands of picea abies (L.) karst. and pinus sylvestris L. and the possibilities to prevent suckers of broad‐leaved trees

Incoming shortwave global radiation (Q _g) and photosynthetically active radiation (PAR; Q _pa as a fraction of full daylight, relative irradiance (%Q), were measured at the same time in young stands of Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.). Measurements were made on three levels above ground: 20 cm above ground and 50 and 15 % of stand height. Stands of three heights (75, 150 and 300 cm) were studied during two months. The stands were created by arranging young trees cut from natural stands, in nine quadratic spacings: 0.1, 0.2, 0.3, 0.4, 0.5, 0.7, 1.0, 1.4 and 2.0 m. The leaf area index (L) was estimated. Differences in %Q‐values for Q _pa and Q_g in the same species and at the same stand height and level of light measurements above ground were significant only in 150 and 300 cm stands. In 75 cm high stands of Scots pine, the %Q was <60% at spacings <0.2 m and in 75 cm high stands of Norway spruce, the %Q was <60% at spacings <0.3 m. Only at 0.1x0.1–0.3x0.3 m, %Q was <20% in Norway spruce stands. In 150 cm stands %Q<20% was measured at spacings <0.7 m in Norway spruce and <0.5 in Scots pine. In 300 cm stands of Norway spruce it was measured up to 1.2 and in Scots pine <1.1 m. Light extinction coefficients, K and K_g for spruce and pine stands were 0.17–0.40 and 0.16–0.31 respectively. Some practical implications of the study are presented. Lack of light (%Q<10%) as a single factor of seriously suppressed growth and development of broad‐leaved plants and suckers by competition in young stands of spruce and pine only occur in dense stands 0.3x0.3 m‐1.1xl.l m (8000–100000 stems/hectare). Competition by light on a regenerated area generally occurs in the level of 50% of tree height (150–300 cm) and higher due to the rapid growth of broad‐leaved trees (sprouts) compared with planted conifers but the light intensity at these levels %Q>10%.     

Nitrogen budgets for Scots pine and Norway spruce ecosystems 12 and 7 years after the end of long-term fertilisation

The magnitude of nitrogen storage and its temporal change in forest ecosystems are important when analysing global change. For example, the accelerated growth of European forests has been linked to increased nitrogen deposition, but the changes in the N inputs that cause long-term changes in ecosystems have not yet been identified. We used two Swedish forest optimum nutrition experiments with Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) to study the long-term fate of N applied to these forest ecosystems. In the pine experiment, in addition to fertiliser (NPK) application, soil acidity was manipulated by application of lime and dilute sulphuric acid. From the spruce experiment, we selected treatments with similar fertiliser doses as in the pine experiment and with and without lime addition.We quantified various terms in the N budget 12 years (pine) and 7 years (spruce) after the last N addition. In the pine stand the NPK-treatment was the only treatment to produce a significant increase in N in the tree biomass (97% above control), whereas in the spruce stand the N additions increased tree N in all treatment combinations (207% above control). In the pine stand the relative distribution of nitrogen between trees and soil did not vary across treatments, with trees containing around 12% of ecosystem N and humus containing around 44% of soil N. The increases in N stocks in the pine stands were mainly in the soil. In contrast, in the spruce ecosystem trees accumulated most of the added N and the increase in the soil was restricted to the humus layer.In the pine ecosystem, large losses of added N (between 254 and 738 kg ha⁻¹ out of 1040 kg ha⁻¹ added as fertiliser) occurred, whereas in the spruce ecosystem we recovered more N than could be accounted for by inputs (between 250 and 591 kg ha⁻¹). There was no clear pattern in the interaction between acidification/liming and N additions.     

Carbon and nitrogen dynamics in topsoils along forest conversion sequences in the Ore Mountains and the Saxonian lowland, Germany

Carbon and nitrogen stocks and their medium-term and readily decomposable fractions in topsoils were compared in relation to soil microbial biomass and activity along sequences from coniferous to deciduous stands. The study was carried out in the Ore Mountains and the Saxonian lowland, representing two typical natural regions in Saxony, Germany. In accordance with current forest conversion practices, the investigation sites represent different stands: mature conifer stands of Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) (type A); Norway Scots spruce and pine with advanced plantings of European beech (Fagus sylvatica L.) or European beech/Common oak (Quercus petreae Liebl.) (type B); and mature deciduous stands of European beech and European beech/Common oak (type C). The investigated forest sites can be grouped into three silvicultural situations according to the development from coniferous stands to advanced plantings and finally mature deciduous forests (chronosequence A–B–C). The organic layer (L, F and H horizons) and uppermost mineral soil (0–10 cm) were analysed for potential C mineralisation, microbial biomass, concentrations of total C and N (TOC and TN) and for medium-term and readily decomposable C and N fractions, obtained by hot- and cold-water extraction respectively. The results showed an increase in organic layer thickness and mass as well as TOC and TN stocks along the forest sequences in the lowland. Yet, underplanted sites with two storeys revealed higher organic layer mass as well as TOC and TN stocks as compared to coniferous and deciduous stands. Stocks of hot- and cold-water-extractable C and N in relation to microbial biomass and its activity revealed a high turnover activity in deeper organic horizons of deciduous forests compared to coniferous stands. The stand-specific differentiation is discussed in relation to microbial biomass, litter quantity and quality and forest structure, but also with respect to the site-specific climatic factors and water budget as well as liming and fly-ash impacts. Results indicate higher dynamics in deciduous stands in the lowland especially during the initial turnover phase. The elevated microbial activity in deeper organic horizons of deciduous litter-influenced sites in spring is discussed as a specific indicator for long-term C sequestration potential as besides C mineralisation organic compounds are humified and thus, can be stored in the organic layer or in deeper soil horizons. Due to liming activities, stand-specific effects on organic matter turnover dynamics have evened out today in the Ore mountain region, but will presumably occur again once base saturation decreases. Here, the stand-specific effect on microbial biomass can currently be seen again as C_mic in the L horizon increased from spruce to beech. Our study sites in the lowland revealed no significant fly-ash impact. Differences between sites were evaluated by calculating the discriminance function. TOC and TN as well as medium-term degradable C and N were defined in this study as indicators for turnover dynamics along forest conversion sites.     

The spreading of the S type of Heterobasidion annosum from Norway spruce stumps to the subsequent tree stand

The occurrence of Heterobasidion annosum in stumps and growing trees was investigated on 15 forest sites in southern Finland where the previous tree stand had been Norway spruce (Picea abies) infected by H. annosum, and the present stand was either Scots pine (Pinus sylvestris), lodgepole pine (Pinus contorta), Siberian larch (Larix siberica), silver birch (Betula pendula) or Norway spruce 8–53 years old. Out of 712 spruce stumps investigated of the previous tree stand, 26.3% were infected by the S group and 0.3% by the P group of H. annosum. The fungus was alive and the fruit bodies were active even in stumps cut 46 years ago. In the subsequent stand, the proportion of trees with root rot increased in spruce stands and decreased in stands of other tree species. On average, one S type genet spreading from an old spruce stump had infected 3.0 trees in the following spruce stand, 0.5 trees in lodgepole pine, 0.3 trees in Siberian larch, 0.05 trees in Scots pine and 0.03 trees in silver birch stand. Although silver birch generally was highly resistant to the S type of H. annosum, infected trees were found on one site that was planted with birch of a very northern provenance.     

Infection experiments with Gremmeniella abietina on seedlings of Norway spruce and Scots pine

Conidia of Gremmeniella abietina infected and caused disease symptoms in annual shoots of both Scots pine (Pinus sylvestris) and Norway spruce (Picea abies) seedlings. In Norway spruce shoots the infection remained largely latent, with only a few seedlings showing symptoms. Mycelial growth inside the shoots was faster in Scots pine than in Norway spruce and was favoured by low temperature in both hosts. The shoots of Norway spruce seedlings had higher endophyte populations than those of Scots pine, and the populations were decreased by low temperatures. Reductions in the normal epiphytic or endophytic flora by acid mist treatments seemed to favour the development of G. abietina.     

Damage by pine weevil Hylobius abietis to conifer seedlings after shelterwood removal

Abstract

Pine weevil (Hylobius abietis L.) damage to seedlings after overstorey removal was investigated in a survey study in six shelterwoods in the south–central part of Sweden. The shelterwoods predominantly consisted of Scots pine, except at one site where the shelter trees mainly consisted of Norway spruce. Before final cutting, 10 plots were laid out at each site and measurements of shelter trees and marked seedlings were taken. The seedlings were examined during the 2 years after final cutting. The study showed that removal of shelter trees increases the risk of severe damage by pine weevil and the variable that was most strongly correlated with the risk was the seedling root collar diameter. Both Scots pine and Norway spruce seedlings were severely damaged by pine weevil, and most of the feeding occurred during the first year after cutting. The amount of debarked area was significantly larger for Scots pine than for Norway spruce seedlings. Vitality (growth of the leading shoot before final cutting) of the seedlings also affected the probability of damage. Seedlings with high vitality were less damaged by pine weevil than seedlings with low vitality. For Scots pine the shelterwood density before final cutting was correlated to the intensity of pine weevil feeding after cutting. In conclusion, after the final cutting of a pine or spruce shelterwood, pine weevils will probably invade the area. To avoid serious damage, Norway spruce and Scots pine seedlings should have reached a diameter of at least 10–12 mm.     

Relationships between insect diversity and habitat characteristics in plantation forests

A methodological approach to the identification of biodiversity indicators in commercial forest stands is illustrated by analysis of the relationships between syrphid (hoverflies) and carabid (ground beetles) community composition and diversity, and stand structure and field layer vegetation. Data were collected from 12 commercial forest sites encompassing a range of climatic conditions and different crop types (Scots pine, Sitka spruce, Norway spruce and Corsican pine) across the UK. Comparisons were also made between unmanaged semi-natural Scots pine woods and Scots pine plantations. For both syrphids and carabids, no differences in species richness and diversity were recorded between semi-natural stands and plantations; one rare syrphid considered to be restricted to semi-natural pine stands was also found in spruce. Syrphid species diversity and richness was higher in southern spruce sites than in the northern sites. Northern sites had distinctive carabid communities, as did sites in the New Forest, a large ancient woodland in southern England. Of the measured habitat variables, vertical stand structure showed the best correlation with species richness and diversity of both carabids and syrphids. Richness and diversity were less in stands with high vertical cover values for canopy layers. Stands with higher field layer cover supported greater syrphid diversity, but lower carabid diversity. Measures of stand structure could be used as potential indicators of syrphid and carabid diversity, but additional habitat parameters also need to be tested.     

The Macedonian Pine, (Pinus peuce Grisebach) in the Balkans and Great Britain

Macedonian pine is little known in Britain as a forest tree.Information comes mainly from its native range in the Balkanmountains, and from specimen trees and young forest plots inBritain. Following a visit in 1982 to Yugoslavia and Bulgaria,the author describes the site conditions and ecological relationsof this species to Scots pine, Norway spruce and Silver fir.Early growth is characteristically slow, even on favourablesites, though it improves after 6–10 years and basal areaincrement may later exceed that of other pines. Growth and behaviourin British stands (mainly 20 years old, but a few older ones)is recorded. Stands of P. peuce are typically healthy and haveexcellent form. Insect and fungal damage is minimal. Early timbertests show specific gravity and strength are low, but the woodis very stable in drying and could have a use in joinery. Seedfrom selected stands will now be used for provenance testing.     

Economics of Forest Thinnings and Rotation Periods for Finnish Conifer Cultures

In this study simultaneous optimization of thinnings and clear-cutting was investigated. The density-dependent whole-stand model was specified for all relevant Finnish Norway spruce (Picea abies (L.) Karst.] and Scots pine (Pinus sylvestris L.) site indices and solved by non-linear programming. Sensitivity analysis showed that in some cases and owing to endogenous thinnings the optimal rotation length may increase with the rate of interest and site fertility, and decrease with harvesting cost. The number of thinnings is more sensitive to changes in the rate of interest, logging conditions and site productivity for Scots pine stands than for Norway spruce stands. Economic optimization suggests that for both species the first thinning should be performed later than officially recommended. The last thinning should be heavier than officially recommended, especially at high rates of interest. This increases the optimal rotation length compared with solutions under restricted thinning intensity.