Low- to moderate-severity historical fires promoted high tree growth in a boreal Scots pine forest of Norway

Abstract

Fire is the most important ecological factor governing boreal forest stand dynamics. In low- to moderate-severity fires, the post-fire growth of the surviving trees varies according to fire frequency, intensity and site factors. Little is known about the growth responses of Scots pine (Pinus sylvestris L.) following fires in boreal forests. We quantified changes in tree growth in the years following 61 historical forest fires (between 1210 and 1866) in tree-ring series collected from fire-scarred Scots pine trees, snags and stumps in Trillemarka nature reserve in south-central Norway. Basal area increment 10 years pre-, 5 years post-, and 11–20 years post-fire were calculated for 439 fire scars in 225 wood samples. We found a slight temporary growth reduction 5 years post-fire followed by a marked growth increase 11–20 years post-fire. Beyond 20 years post-fire, the long-term tree growth declined steadily up to approximately 120 years. Our results indicate that recurring fires maintained high tree growth in remnant Scots pines, most probably due to a reduction in tree density and thus decreased competition.     

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.     

Equations for estimating above- and belowground biomass of Norway spruce,Scots pine,birch spp. and European aspen in Latvia

This study aims to derive allometric functions to estimate the above- and belowground biomass components of the most important tree species in Latvia. The study material included a total of 81 Norway spruce (Picea abies [L.] Karst), 102 Scots pine (Pinus sylvestris L.), 105 birch spp. (mainly silver birch (Betula pendula Roth)) and 84 European aspen (Populus tremula L.) trees sampled in 124 forest stands. The suitability of three mathematical models for the prediction of total aboveground biomass, stem biomass, total live and dead branch biomass, belowground biomass and small root biomass was evaluated. Our analysis revealed that the use of the Intergovernmental Panel on Climate Change mean default values for the root-to-shoot ratio recommended for temperate and boreal ecological zones leads to the overestimation of root biomass of young trees, especially Scots pine and Norway spruce. Our findings indicate that biomass functions recommended for other Baltic Sea countries are not appropriate for the assessment of the biomass stock in Latvia’s forests because these lead to biased estimates. The biomass functions derived in our study are recommended for reporting the biomass stock in Latvia.     

Growth patterns from different forest generations of Scots pine in Estonia

There is strong evidence that climate change alters tree growth in boreal forests. In Estonia, the analysis of ring measurements has been a common method to study growth changes. In this study, annual height growth data from dominant or co-dominant Scots pine (Pinus sylvestris L.) trees were used to develop a growth model for three forest generations. Stem analysis was applied and annual height growth was measured as the distance between whorls, as detected by branch knots of whorls on the split stem surface. Retrospective analysis of height growth produced comparative trends for three different age groups. Statistical analyses were used to estimate the impact of different factors on growth. Annual height growth was considered the best indicator for detecting possible trends in the growth potential of trees. Study results indicate that three generations (separated by time periods of 30–40 years) showed significant differences in growth patterns caused by shifts in climatic factors and management regimes (anthropogenic and natural disturbances).     

The effects of pine mistletoe (Viscum album subsp. austriacum) on the growth of Scots pine and Crimean pine in Turkey

In this study, the effect of pine mistletoe (Viscum album subsp. austriacum) on basal area increment of Crimean pine and Scots pine was investigated. Dendrochronological data were collected from 223 (71 uninfected and 152 infected) Crimean pines and 195 (77 uninfected and 118 infected) Scots pines located in Kastamonu province of Turkey in 2014. Infected sample trees were classified as light, moderate or severe infection levels. Growth trends and basal area increment loses were compared between uninfected and infected trees for the periods of the last 10, 20 and 30 years. In addition, infection status of forest stands was investigated using temporary sample plots; 27 plots in Crimean pine stands and 26 plots in Scots pine. Results demonstrated that basal area increments were negatively affected by pine mistletoe for both species. Mean basal area increment losses of infected trees for the last decade were determined as 24% for Scots pine and 26% for Crimean pine. Basal area increment losses varied by infection levels (light, moderate and severe) as follows: 25%, 20% and 28% for Scots pines and 20%, 32% and 9% for Crimean pines. Scots pine stands were more severely infected by pine mistletoe than Crimean pine stands. There were negative correlations between number of infected trees and stand density for both species, while positive correlation was detected between the number of infected trees and mean diameter for Scots pine. The results of this study indicate that the pine mistletoe infection has negative effect on radial growth of Scots pine and Crimean pine trees. The results can be an important contribution to the forest management and protection activities in mistletoe-infected stands.     

Evaluation of competitive effects of green alder,willow and other tall shrubs on white spruce and lodgepole pine in Northern Alberta

In boreal forests of western Canada, lodgepole pine (Pinus contorta Dougl. ex. Loud.) and white spruce (Picea glauca (Moench) Voss) often grow together with numerous tall shrubs such as green alder (Alnus crispa (Ait.) Pursh) and little-tree willow (Salix spp.). In an area south of Grande Prairie, Alberta, Canada, we examined the effects of shrubs, herbs and other trees on nutrient and light availability and growth of white spruce and lodgepole pine. For white spruce the best competition measure (tested against volume increments of the past 3 years) was visually estimated % ground cover times the height of the competitor (VCHT) with light (DIFN) ranking in third place. For lodgepole pine, DIFN was the best competition measure for predicting volume increment and the best competition index was again VCHT. Taller conifers had a stronger competitive effect than tall shrubs, with their effect on white spruce being larger than that on lodgepole pine.     

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.     

Swedish lodgepole pine seed orchard crops tested in north-west Russia

Abstract

Tree vitality and height of lodgepole pine (Pinus contorta var. latifolia) originating from the six Swedish seed orchards and native Scots pine (Pinus sylvestris L.) were estimated in three 8-yr-old test plantations established in the Komi Republic (north-west Russia). A randomized row-plot design with 9–13 replicates of each entry was used. In general, the Scots pine tree vitality was better than that of lodgepole pine but these differences were significant only for seed sources of southern origins Larslund, Rumhult, and Österby. On the contrary, the lodgepole pine height growth was faster (6–21%) except for seed sources of southern origins Rumhult and Österby. In comparison with the native Scots pine, lower mean heights (4–10%) were recorded for these seed sources. Among the lodgepole pine seed sources the northern origins had better vitality, while the effect of latitude on the tree height was insignificant.     

Afforestation of low-productivity peatlands in Sweden — the potential of natural seeding

In 1971, a series of five afforestation trials were established along a north-south gradient on open peatlands in Sweden. All areas were drained, fertilized and planted with Scots pine (Pinus sylvestris). Survival and height of the planted trees as well as the amount of natural establishment, i.e. downy birch (Betula pubescens), silver birch (Betula pendula), Norway spruce (Picea abies (L.) Karst.), Scots pine (Pinus sylvestris L.), and other deciduous species: (e.g. Salix sp., Sorbus aucuparia), by seeding from nearby forests were measured 18–22 years later. The amount of naturally established trees exceeded the number of living planted trees in all five areas. Next to downy birch, Scots pine was the most common naturally established species. Large variations in both amount and height of natural establishment were found along the climatic gradient. Planted trees were taller than naturally established trees, except for the northernmost area. Number and height of naturally established trees correlated positively to closeness to nearest forest and to nearest ditch. These trees also responded positively to PK fertilization in the three southernmost areas. In the two northernmost areas no such response was found. It was concluded that natural seeding from neighbouring forests can be counted on and recommended in afforestation of low-productive peatlands in Sweden, provided that downy birch is accepted as a dominant tree species.     

Modeling individual tree height growth of Norway spruce and Scots pine from national forest inventory data in Norway

We developed individual tree height growth models for Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.) in Norway based on national forest inventory data. Potential height growth is based on existing dominant height growth models and reduced due to competition by functions developed in this study. Three spatially explicit and two spatially non-explicit competition indices were tested. Distance effects and diameter ratio effects were estimated from the data simultaneously with parameters of the potential modifier functions. Large height measurement errors in the national forest inventory data caused large residual variation of the models. However, the effects of competition on height growth were significant and plausible. The potential modifier functions show that height growth of dominant trees is largely unaffected by competition. Only at higher levels of competition, height growth is reduced as a consequence of competition. However, Scots pine also reduced height growth at very low levels of competition. Distance effects in the spatially explicit competition indices indicated that the closest neighbors are most important for height growth. However, for Scots pine also competitors at larger distance affected height growth. The five competition indices tested in this study explained similar proportions of the variation in relative height growth. Given that unbiased predictions can only be expected for the same plot size, we recommend a spatially explicit index, which describes the distance function with a negative exponential, for use in growth simulators.     

Quantifying the effect of pine mistletoe on the growth of Scots pine

Mistletoe infection results in substantial growth losses in mistletoe‐infected forests. This study reports and evaluates the results of retrospective analyses of radial growth of Scots pine (Pinus sylvestris) in relation to the level of infection of pine mistletoe (Viscum album ssp. austriacum). A total of 43 Scots pine trees were destructively sampled from different sites. Of these trees, 14 were uninfected and 29 were infected. Infection classes were determined using six‐class dwarf mistletoe rating system (DMRS). All needle and mistletoe biomass were removed completely and weighed for each sampled tree. Subsamples from needles and all mistletoe biomass were taken to the laboratory for oven‐dried weight determinations. Five‐cm‐thick wood discs were cut from the stem at the breast height (1.3 m) to determine annual basal area increment for the last 25 years. In addition to DMRS, new infection classes were created using mistletoe‐to‐needle biomass (MB/NB) ratio. The results showed that the radial growth losses could be as much as 41% to 64% at different infection levels. The rate of growth loss in relation to DMRS and MB/NB ratio was similar, but with a larger variability in DMRS values. The results showed that both DMRS rating and MB/NB ratio seem to be important for quantifying growth loss on Scots pine trees infected with mistletoe. The results of this study can also be invaluable in modelling the effects of mistletoe on the growth of Scots pine trees.     

CLIMATE AND SILVICULTURAL IMPLICATIONS IN MODIFYING STAND COMPOSITION IN MIXED FIR-PINE STANDS

ABSTRACT

A growing concern exists over the decreasing proportion of Scots pine (Pinus sylvestris L.) trees in mixed Trojan fir (Abies nordmanniana subsp. equi-trojani [Asch. & Sint. Ex Boiss] Coode & Cullen)-Scots pine forests in northern Turkey. Given the changes in mean annual temperature and annual precipitation for the last 40 years in the region, understanding of the sensitivity of Trojan fir and Scots pine trees to changing climate seems to be critical so that better management strategies can be developed against the potential climate extremes of the future in the region. Moreover, our knowledge on the influence of current silvicultural methods on seedling density and growth in these forests is limited. Therefore, in this study, the growth response (i.e., radial growth) of Trojan fir and Scots pine trees to the changing climate were examined. In addition, the influence of current silvicultural practices on seedling growth and density in these forests was also monitored. Trojan fir appeared more sensitive to the climatic variables (i.e., temperature and precipitation) than Scots pine in the region. It was also found that the current silvicultural practices might favor Trojan fir over Scots pine in these forests. Natural dynamics and current silvicultural implications would benefit Trojan fir, however, given the species’ potential sensitivity to the changing climate, current silvicultural approaches can be modified to favor Scots pine, and to increase the resilience of these forests against climate extremes expected in the region’s future.     

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.     

Superoxide dismutase (SOD) activity in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies L. Karst.) needles in northern Finland

The superoxide dismutase (SOD EC 1.15.1.1) activity in Scots pine (Pinus sylvestris) and Norway spruce (Picea abies L. Karst.) needles in urban and rural trees of northern Finnish populations was studied. Enzyme activity was higher in pine than in spruce needles. Two pine clones from eastern Finland and Lapland revealed great differences in specific SOD enzyme activity.     

The effect of girdling on the moisture content of small-sized trees

In this study, the effect of girdling on the moisture content of small-sized trees for heat energy production was clarified. The moisture content was measured for Scots pine (Pinus sylvestris), Norway spruce (Picea abies), and Downy birch (Betula pubescens) during two growing seasons after girdling. The trees were girdled at breast height for around 30 cm by removing the bark, phloem, and cambium from around the stem. At the beginning of the growing season the mean moisture content of the living Scots pine (P. sylvestris) and Norway spruce (P. abies) was 60%, and for Downy birch (B. pubescens) it was 50%. During the first growing season the effect of girdling on the moisture content was low, but during the second growing season the moisture content decreased significantly. The moisture content of the Norway spruce (P. abies) (23%) and Downy birch (B. pubescens) (33%) was at its lowest point at 14 months after girdling. There were no significant changes in the moisture content of the Scots pine (P. sylvestris) in this study. The results of this study can be used in basic research and in the development of energy wood production.     

Stem Form and Taper Changes After Thinning and Nitrogen Fertilization in Picea abies and Pinus sylvestris Stands

Stem form and taper changes after thinning and thinning combined with N fertilization were studied in 23 Norway spruce [Picea abies (L.) Karst.] and 46 Scots pine (Pinus sylvestris L.) stands in Sweden observed for 5-28 yrs. Average taper was calculated for the stem section 1.3-6.0 m above ground level and as the ratio between the diameter at breast height and total tree height for periods of 5-10 yrs. At the start of the experiment, before the first thinning, the dominant height was 12-15 m. Once 65% of the basal area had been removed in a single thinning from below, the remaining trees showed a strong increase in taper compared with trees in unthinned stands. Stems in stands treated with heavily recurrent thinnings from below also increased in taper, although the increases were not always statistically significant. Trees in thinned, N-fertilized Scots pine stands in middle and northern Sweden developed a more pronounced taper compared with stems in equally thinned, unfertilized stands.     

Growth and productivity of black spruce in even- and uneven-aged stands at the limit of the closed boreal forest

The increasing commercial interest and advancing exploitation of new remote territories of the boreal forest require deeper knowledge of the productivity of these ecosystems. Canadian boreal forests are commonly assumed to be evenly aged, but recent studies show that frequent small-scale disturbances can lead to uneven-aged class distributions. However, how age distribution affects tree growth and stand productivity at high latitudes remains an unanswered question. Dynamics of tree growth in even- and uneven-aged stands at the limit of the closed black spruce (Picea mariana) forest in Quebec (Canada) were assessed on 18 plots with ages ranging from 77 to 340 years. Height, diameter and age of all trees were measured. Stem analysis was performed on the 10 dominant trees of each plot by measuring tree-ring widths on discs collected each meter from the stem, and the growth dynamics in height, diameter and volume were estimated according to tree age. Although growth followed a sigmoid pattern with similar shapes and asymptotes in even- and uneven-aged stands, trees in the latter showed curves more flattened and with increases delayed in time. Growth rates in even-aged plots were at least twice those of uneven-aged plots. The vigorous growth rates occurred earlier in trees of even-aged plots with a culmination of the mean annual increment in height, diameter and volume estimated at 40–80 years, 90–110 years earlier than in uneven-aged plots. Stand volume ranged between 30 and 238 m³ ha⁻¹ with 75% of stands showing values lower than 120 m³ ha⁻¹ and higher volumes occurring at greater dominant heights and stand densities. Results demonstrated the different growth dynamics of black spruce in single- and multi-cohort stands and suggested the need for information on the stand structure when estimating the effective or potential growth performance for forest management of this species.     

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%.     

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.     

Assessment of bias due to random measurement errors in stem volume growth estimation by the Swedish National Forest Inventory

Abstract

We evaluated the performance of two methods for estimating stem volume increment at individual tree level with respect to bias due to random measurement errors. Here, growth is either predicted as the difference between two consecutive volume estimates where single-tree volume functions are applied to data from repeated measurements or by a regression model that is applied to data from a single survey and includes radial increment. In national forest inventories (NFIs), the first method is typically used for permanent plots, the second for temporary plots. The Swedish NFI combines estimates from both plot types to assess growth at national and regional scales and it is, therefore, important that the two methods provide similar results. The accuracy of these estimates is affected by random measurement errors in the independent variables, which may lead to systematic errors in predicted variables due to model non-linearity. Using Taylor series expansion and empirical data from the Swedish NFI we compared the expected bias in stem volume growth estimates for different diameter classes of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.). Our results indicate that both methods are fairly insensitive to random measurement errors of the size that occur in the Swedish NFI. The empirical comparison between the two methods showed greater differences for large diameter trees of both pine and spruce. A likely explanation is that the regressions are uncertain because few large trees were available for developing the models.