Effects of photoperiod and temperature on the timing of bud burst in Norway spruce (Picea abies)

We examined the effects of several photoperiod and temperature regimes imposed during the winter-spring period on the timing of bud burst in rooted cuttings of Norway spruce (Picea abies (L.) Karst.) grown in a greenhouse in Finland. The treatments were initiated in November and December after the cuttings had been exposed to natural chilling and freezing events. Irrespective of the treatments applied, time to bud burst decreased with increased duration of previous exposure to natural chilling and freezing events. Fluctuating day/night temperatures and continuous lengthening of the photoperiod hastened bud burst. Shortening the photoperiod delayed bud burst, suggesting that little or no ontogenetic development toward bud burst takes place during mild periods before the winter solstice. In the case of climatic warming, this phenomenon may prevent the premature onset of growth that has been predicted by computer simulations with models that only consider temperature regulation of bud burst.     

Ectomycorrhizas and cadmium toxicity in Norway spruce seedlings

We studied the effects of ectomycorrhizal colonization by Laccaria bicolor (Maire) Orton S238 and Paxillus involutus (Batsch) Fr. 533 on cadmium (Cd) toxicity in Norway spruce seedlings (Picea abies (L.) Karst.). Both mycorrhizal and nonmycorrhizal seedlings were exposed to 0 (control), 0.5 or 5 &mgr;M CdSO(4) for 9 weeks in a sand culture system with frequent addition of nutrient solutions. In pure culture, P. involutus and L. bicolor showed similar Cd tolerance. However, in symbiosis, the Cd treatments decreased colonization by L. bicolor but not by P. involutus. Paxillus involutus ameliorated the negative effects of 0.5 &mgr;M Cd on shoot and root growth and chlorophyll content of old needles, whereas L. bicolor did not. Mycorrhizal colonization did not affect Cd concentrations of old needles and roots of seedlings. Despite differences between the ectomycorrhizal fungi in colonization and ability to alleviate Cd toxicity of seedlings, both species reduced Cd concentrations of young needles to a similar degree compared with nonmycorrhizal seedlings. However, in the 0.5 &mgr;M Cd treatment, the Cd content of needles of seedlings colonized by P. involutus was increased, whereas the Cd content of needles of seedlings colonized by L. bicolor was similar to that of needles of nonmycorrhizal seedings. When the amount of Cd translocated to needles was expressed on a root length basis to account for differences in the size of the root systems, the amount of Cd translocated to the needles was similar in seedlings mycorrhizal with P. involutus and in nonmycorrhizal seedlings. All mycorrhizal seedlings were similarly affected by 5 &mgr;M Cd, indicating that the amelioration efficiency of ectomycorrhizal fungi is dependent on the metal concentration to which the roots are exposed. Concentrations of P, K, Ca, Mg and Mn were decreased by 5 &mgr;M Cd to a similar extent in both nonmycorrhizal and mycorrhizal seedlings. In contrast to L. bicolor, P. involutus increased P uptake and altered patterns of root branching. We conclude that mycorrhizas alleviate Cd-induced reductions in growth of Picea abies seedlings. Although the two mycorrhizal fungi examined differed in their ability to alleviate Cd toxicity, these differences were not related to differences in Cd uptake or translocation to the shoot of the mycorrhizal seedlings. We suggest that amelioration of Cd toxicity by P. involutus may be a result of improved P nutrition or changes in root morphology, or both.     

Impact of elevated carbon dioxide concentration and temperature on bud burst and shoot growth of boreal Norway spruce

Effects of elevated temperature and atmospheric CO2 concentration ([CO2]) on spring phenology of mature field-grown Norway spruce (Picea abies (L.) Karst.) trees were followed for three years. Twelve whole-tree chambers (WTC) were installed around individual trees and used to expose the trees to a predicted future climate. The predicted climate scenario for the site, in the year 2100, was 700 micromol mol-1 [CO2], and an air temperature 3 degrees C higher in summer and 5 degrees C higher in winter, compared with current conditions. Four WTC treatments were imposed using combinations of ambient and elevated [CO2] and temperature. Control trees outside the WTCs were also studied. Bud development and shoot extension were monitored from early spring until the termination of elongation growth. Elevated air temperature hastened both bud development and the initiation and termination of shoot growth by two to three weeks in each study year. Elevated [CO2] had no significant effect on bud development patterns or the length of the shoot growth period. There was a good correlation between temperature sum (day degrees>or=0 degrees C) and shoot elongation, but a precise timing of bud burst could not be derived by using an accumulation of temperature sums.     

Dormancy release of Norway spruce under climatic warming: testing ecophysiological models of bud burst with a whole-tree chamber experiment

Ecophysiological models predicting timing of bud burst were tested with data gathered from 40-year-old Norway spruce (Picea abies (L.) Karst.) trees growing in northern Sweden in whole-tree chambers under climatic conditions predicted to prevail in 2100. Norway spruce trees, with heights between 5 and 7 m, were enclosed in individual chambers that provided a factorial combination of ambient (365 micromol mol-1) or elevated (700 micromol mol-1) atmospheric CO2 concentration, [CO2], and ambient or elevated air temperature. Temperature elevation above ambient ranged from +2.8 degrees C in summer to +5.6 degrees C in winter. Compared with control trees, elevated air temperature hastened bud burst by 2 to 3 weeks, whereas elevated [CO2] had no effect on the timing of bud burst. A simple model based on the assumption that bud rest completion takes place on a fixed calendar day predicted timing of bud burst more accurately than two more complicated models in which bud rest completion is caused by accumulated chilling. Together with some recent studies, the results suggest that, in adult trees, some additional environmental cues besides chilling are required for bud rest completion. Although it appears that these additional factors will protect trees under predicted climatic warming conditions, increased risk of frost damage associated with earlier bud burst cannot be ruled out. Inconsistent and partially anomalous results obtained in the model fitting show that, in addition to phenological data gathered under field conditions, more specific data from growth chamber and greenhouse experiments are needed for further development and testing of the models.     

Infection of Norway spruce container seedlings by Gremmeniella abietina

First‐ and second‐year containerized Norway spruce seedlings were inoculated with conidia of type A (large tree type) and type B (small tree type) of Gremmeniella abietina var. abietina at different times during the summer. The appearance of symptoms after artificial inoculation and natural infection on spruce seedlings were recorded the following spring and compared with the disease symptoms on Scots pine seedlings. The proportion of diseased seedlings after inoculation reached as high as 80%. The susceptible period during the summer began later on the first‐year seedlings than on the second‐year seedlings, and was similar for the pine seedlings. Susceptibility of first‐year seedlings was highest in August and on second‐year seedlings in July. The accumulated temperature sum, relative humidity and height growth for first‐ and second‐year seedlings was assessed. Natural infection in 2002 caused more disease on pine than on spruce seedlings. Experimental thinning of seedlings had no effect on disease incidence. In a preliminary comparison between the ability of A and B types to cause disease in Norway spruce seedlings, type B caused more damage than type A after inoculation. However, type A caused a high disease frequency in other experiments in this study. Symptoms on Norway spruce seedlings often first occurred in the mid‐section of the shoot, and were similar to those observed on pine seedlings: needles turned brown, starting at the needle base, in the spring following inoculation. On first‐year spruce, diseased needles were shed rapidly, in contrast to a slower rate of shedding on first‐year pine seedlings. Pycnidia developed about 2 years after inoculation (on pine 1 year after inoculation). On Norway spruce seedlings the lower part of the shoot, including the lateral shoots, often remained alive. The experiments show that G. abietina can cause disease on containerized Norway spruce seedlings under nursery conditions in Finland. The coincidence of spore dispersal, seedling susceptibility and predisposing factors are important in disease development.     

Effects of repeated fertilization in young Norway spruce forests

Several studies have shown the positive effect of nitrogen fertilization on conifer growth. In young Norway spruce (Picea abies) stands, an additional effect of including a mixture of other nutrients has often, but not always, been found. We studied effects of repeated fertilization in 28 stands with young Norway spruce in central Norway. The treatments consisted of plots without nutrient addition (Control), fertilization with 150?kg?N?ha^?1 (150?N), and fertilization with 150?kg?N plus addition of P, K, Mg, B, Mn and Cu (150?N?+?mix), repeated three times with approximately eight years interval. There was a clear positive effect on volume increment of the 150?N and 150?N?+?mix treatments compared to Control, and the effect was significantly higher for 150?N?+?mix than for 150?N. Fertilization had a stronger effect in the first fertilization period than in the second, while the third period was intermediate. The effect of 150?N?+?mix was strongest at plots?>?300?m a.s.l. However, this correlation may be due to geological conditions rather than elevation. Further studies are needed to find out under which edaphic conditions a nutrient mixture will increase growth substantially in young spruce stands.     

Development and growth of primordial shoots in Norway spruce buds before visible bud burst in relation to time and temperature in the field

The timing of bud development in ecodormancy is critical for trees in boreal and temperate regions with seasonally alternating climates. The development of vegetative buds and the growth of primordial shoots (the primordial shoot ratio) in Norway spruce were followed by the naked eye and at stereo and light microscopic levels in fresh-cut and fixed buds obtained by regular field samplings during the spring of 2007, 2008 and 2009. Buds were collected from 15 randomly selected trees (all 16 years old in 2007) of one southern Finnish half-sib family. The air temperature was recorded hourly throughout the observation period. In 2008 and 2009, initial events in the buds, seen as accumulation of lipid droplets in the cortex area, started in mid-March and were depleted in late April, simultaneously with the early development of vascular tissue and primordial needles. In mid-April 2007, however, the development of the buds was at least 10 days ahead as a result of warm spells in March and early April. Variation in the timing of different developmental phases within and among the sample trees was negligible. There was no clear one-to-one correspondence between the externally visible and the internal development of the buds. The dependence of the primordial shoot ratio on different types of temperature sum was studied by means of regression analysis. High coefficients of determination (R(2)?≈?95%) were attained with several combinations of the starting time (beginning of the year/vernal equinox), the threshold value (from -3 to +5 °C), and the time step (hour/day) used in the temperature summation, i.e., the prediction power of the primordial shoot ratio models turned out to be high, but the parameter estimate values were not unambiguous. According to our results, temperature sums describe the growth of the primordial shoot inside the bud before bud burst. Thus, the results provide a realistic interpretation for the present phenological models of bud development that are based on temperature sums and external observations of bud burst only, and they also provide new tools for improving the models.     

Seedling cold hardiness, bud set, and bud break in nine provenances of Pinus greggii Engelm.

Cold hardiness and timing of bud set and bud break are important processes that provide protection of nursery seedlings against low temperatures. Seedlings of 9 provenances of Pinus greggii from two different regions of Mexico were tested to determine cold hardiness, bud set, and bud break timing differences. Needle sections were exposed to freezing temperatures to determine an injury index of each provenance. In addition, bud set and bud break timing were recorded through the fall, winter and spring. There were significant differences in cold hardiness between seedlings from northern and southern provenances. At the maximum cold hardiness, the index of injury (LT₅₀) for northern provenances was LT₅₀ = −18 °C, compared to −12 °C for southern provenances. There was a considerable variation among the provenances in the proportion of seedlings that set terminal buds. Seedlings from northern provenances had greater proportions of seedlings that set a terminal bud than seedlings from southern provenances. There were also significant differences in the bud break timing in the following spring among the 9 provenances. Seedlings from northern provenances broke bud earlier than southern provenances. Cold hardiness, bud set, and bud break timing results may be useful to determine how far a specific seed source can be moved from its natural environment.     

Persistence of deltamethrin against Hylobius abietis on Norway spruce seedlings

Abstract

The pine weevil Hylobius abietis L. is major threat to forest regeneration in the Nordic countries. The persistence of the deltamethrin insecticide used against pine weevil on Norway spruce seedlings was studied after the seedlings were dipped or sprayed. Insecticide application was timed to occur either before or after frozen storage. Bioassays with the stems of Norway spruce seedlings were used to determine the effect of the insecticide against feeding by the pine weevil. The measures of the control effect were reduction in area of gnawed bark and the state of health of the pine weevils. The concentration of deltamethrin decreased rapidly in seedlings, especially after spraying treatment, which did not efficiently protect seedlings against the pine weevil 6 weeks after planting. There were no signs of degradation of deltamethrin or of an effect on seedling height after frozen storage. In bioassay, the amount of deltamethrin that efficiently prevented feeding by the pine weevil was 5.5 µg g^?1 fresh weight. After one growing season in the field, about 1.76–2.24 µg g^?1 (13–15% of the initial level) of dipped deltamethrin remained in the seedlings. In seedlings treated by spraying, 0.93–0.98 µg g^?1 (7–8% of the initial level) of the deltamethrin remained. According to bioassays, these amounts were no longer sufficient to protect seedlings from feeding by the pine weevil. Therefore, in the first summer, dipping was a significantly more efficient method of application for control of pine weevils.     

Hebeloma inoculation on Norway spruce seedlings in solarized and infested soil

The effect of inoculation of Hebeloma sp. on the growth of Norway spruce (Picea abies) seedlings was studied, in a controlled environment, with soil samples naturally infested by Pythium spp., Fusarium spp. and Rhizoctonia solani, and with samples of soil in which the pathogens had been controlled by solarization. The best results were obtained in solarized soil, but mycorrhizae also enhanced plant growth in the presence of the whole soil-borne mycoflora. The combined use of inoeulation of a mycorrhizal fungus and solarization is discussed.     

Impact of soil pressure and compaction on tracheids in Norway spruce seedlings

We tested the effect of soil compaction on Norway spruce seedlings in terms of the size and theoretical volume flow rate of the tracheids. The results show that soil pressure limits growth in the diameter of the lumens of tracheids in all parts of seedlings studied. The tracheids of the roots with primary xylem had larger lumens than those of the roots and shoots with secondary xylem in both unloaded and loaded seedlings. This corresponds to the higher cumulative theoretical volume flow rate of the tracheids from roots with primary xylem than those from roots and shoots with secondary xylem. Although the volume flow rate of tracheids, according to the Hagen-Poiseuille law, was directly proportional to the quadratic power of the capillary diameter (tracheid lumen), the cumulative curve of the theoretical hydraulic volume flow rate was higher or relatively comparable in loaded seedlings. An explanation for these findings is that there were higher gradients of water potential values in roots and leaves in loaded seedlings because the lengths of the conductive pathways were 27% shorter than in unloaded seedlings. We hypothesise that trees have adapted to different stresses by shortening their conductive pathways to maintain a transpiration rate similar to that of non-stressed trees. These results concerning the impact of soil compaction on tracheid diameter and volume flow rate improve our understanding of the growth and functioning of different conifer organs and the mechanisms underlying the efficiency of water transport through the root xylem to the shoot.     

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.     

Growth and biomass partitioning of nine provenances of Quillaja saponaria seedlings to water stress

Information on the morphological and physiological responses of seedlings to stressors, such as water stress, is required for successful early establishment of seedlings. We examined provenance variation in morphological and physiological traits of Quillaja saponaria Molina seeds from nine provenances representing a latitudinal transect across the species range in Chile. The seedlings were subjected to two water regimes (well-watered vs water restriction) in a nursery experiment, and growth, biomass, survival, and gas exchange traits were measured. As expected, well-watered seedlings exhibited a superior performance in all traits analysed. Provenance effects were significant for most of the morphological and physiological traits. In the growth and biomass analysis, the northernmost provenance showed the lowest survival, growth and dry biomass, whereas in the gas exchange analysis, the southern interior provenance showed the highest net photosynthesis, transpiration, stomatal conductance and water use efficiency. The interaction between water regimes and provenance was only significant for diameter and net photosynthesis. These results indicate that different provenances of Q. saponaria show a stable performance across different controlled drought conditions. This information is of relevance for sourcing seeds for the restoration of the species.     

Climatic factors controlling the productivity of Norway spruce: A model-based analysis

The process-based growth model, BIOMASS, was modified to incorporate low-temperature effects on photosynthetic production in Norway spruce (Picea abies) stands growing in northern Sweden. The low-temperature features incorporated in BIOMASS made it possible to simulate and estimate the reduction in photosynthetic rates caused by boreal conditions. The following four simulation-scenarios were used: (i) ‘potential' photosynthesis without boreal restrictions; (ii) reduction caused by a frozen soil; (iii) reduction caused by incomplete recovery of photosynthetic capacity during spring as a result of damage caused by low winter temperatures; and (iv) reduction as an effect of frost-induced autumn decline. Annual photosynthetic production (or gross primary production (GPP)) was simulated for three calendar years, 1990–1992, for stands with low (control) and high (irrigated and fertilized) nutrient availability. The reduction of ‘potential' GPP, caused by the low-temperature effects, ranged from 35–44% for control (C) and from 34–42% for irrigated-fertilised (IL) stands, respectively. The most pronounced loss of ‘potential' GPP originated from reduced photosynthetic capacity, in spring and early summer, which led to losses of 21–28% for C and 19–26% for IL stands. The variation between years differed mainly as an effect of differences in spring temperatures, which resulted in different rates of recovery of photosynthetic capacity. Reductions caused by frozen soil and low photosynthetic capacity during winter were similar in C and IL stands (12–13%), as were the losses resulting from severe autumn frosts (3–4%). It is concluded that, unless the effects of frozen soils and reduced photosynthetic capacity during spring and early summer are considered, large errors (ca. 40%) will be introduced into estimates of the annual photosynthetic production of boreal conifer forests.     

Photosynthesis in Norway spruce seedlings infected by the needle rust Chrysomyxa rhododendri

Chrysomyxa rhododendri (DC.) De Bary is a needle rust with a host shift between Rhododendron sp. and Norway spruce (Picea abies (L.) Karst.), penetrating only the new developing flushes of the conifer. Because little is known about its effects on trees, we investigated several parameters related to photosynthesis in artificially infected 3-year-old Norway spruce seedlings. The potential efficiency of photosystem II (PSII; derived from chlorophyll fluorescence measurements) was reduced in infected current-year needles as soon as disease symptoms were visible, about three weeks after inoculation. Two weeks later, photosynthetic O(2) evolution (P(max)) of infected needles was less than 20% of control needles, whereas respiratory O(2) uptake (R(D)) was about three times higher than that of control needles. Nonstructural carbohydrate concentrations were about 60% of control values in all parts of the shoots of infected trees. Photosynthetic inhibition was associated with marked decreases in chlorophyll concentration and chlorophyll a/b ratio but only a small reduction in carotenoid concentration. In infected trees, P(max) of noninfected 1-year-old and 2-year-old needles was 50 and 80% higher than in the corresponding age class of needles of control trees. Estimation of potential daily net dry mass production, based on P(max), R(D), specific leaf area, carbon content and needle biomass, indicated that seedlings infected once were able to produce 60%, and those infected twice only 25%, of the dry mass of controls. We conclude that afforestation and regeneration of Norway spruce is seriously impaired in regions where seedlings are frequently attacked by Chrysomyxa.     

Comparison of the virulence of Armillaria cepistipes and Armillaria ostoyae on four Norway spruce provenances

The basidiomycetes Armillaria cepistipes and Armillaria ostoyae frequently occur in the same forest stand. In this study, we determined the virulence of 20 isolates of A. cepistipes and 16 isolates of A. ostoyae on four different provenances of 2‐year‐old Norway spruce (Picea abies). Within 30 months after inoculation, 1.1 and 19.1% of the seedlings inoculated with A. cepistipes and A. ostoyae, respectively, had died or were dying. The incidence of dead and dying seedlings varied between 3 and 49% among the A. ostoyae isolates. The virulence of an isolate was positively correlated to its ability to produce rhizomorphs. One Norway spruce provenance showed significantly lower susceptibility to A. ostoyae than the other three. Rhizomorphs of both Armillaria species were attached to the root surface. The attached rhizomorphs of A. ostoyae, however, were associated with significantly more lesions. The virulence of the isolates was not correlated with their wood‐degrading capability for either of the Armillaria species.     

Influence of nutrient supply on spring frost hardiness and time of bud break in Norway spruce (Picea abies (L.) Karst.) seedlings

When spring frosts occur on recently planted forest sites, severe damage may occur to the seedlings. The aim of the present study was to test how different low levels of nutrient concentrations in Norway spruce (Picea abies (L.) Karst.) seedlings affected spring frost hardiness and time of bud break. Seedlings were grown in a greenhouse for one season and supplied with fertiliser containing 22, 43 and 72 mg N l^–1, respectively. The treatments resulted in needle nitrogen concentrations ranging from 0.9 to 1.8% in autumn. After winter storage at 0 °C, bud break was recorded on seedlings growing in the greenhouse, outdoors and in growth chambers at 12 °C and at 17 °C. Freezing tests were performed on seedlings directly removed from winter storage and following one week growth in the greenhouse. Seedlings receiving fertiliser with 43 mg N l^–1 had less freezing injury than the two other fertilisation treatments in the present study. The earliest bud break occurred in seedlings receiving 72 mg N l^–1.     

Induction of callose in roots of Norway spruce seedlings after short-term exposure to aluminum

Callose (1,3-beta-glucan) is a suggested physiological indicator of aluminum (Al) toxicity in crop plants. It is not known if callose serves a similar function in forest trees, because quantitative data on callose formation in tree roots are limited, particularly under controlled conditions. To evaluate callose as a physiological indicator of Al toxicity in tree roots, we quantified callose formation in roots of Norway spruce (Picea abies (L.) Karst.) seedlings. Seedlings were grown in simulated soil solutions in the presence or absence (control) of Al under controlled conditions. In seedlings grown in solutions containing 280 microM Al, callose concentrations in roots were twice as high as control values after 6 h of Al treatment and 5 times higher than control values after 1 day. Thereafter, root callose concentrations gradually decreased and were only twice as high as control values after 7 days. The presence of various Al concentrations in the simulated soil solutions indicated that callose was induced by a relatively low Al concentration (84 microM). We conclude that callose in tree roots is an indicator of Al toxicity.     

Effects of compost additive in sphagnum peat growing medium on Norway spruce container seedlings

Sphagnum peat has been the most commonly used growing medium in containers in tree nurseries worldwide for its good growing properties. As a result of increasing costs and environmental incentives, seedling-growers are seeking more local growing medium components such as composts. Composts are, however, diverse products with varying chemical, physical, and hygienic properties and therefore require thorough testing before real-world use. In this study, a commonly used compost (raw materials: sewage sludge, biowaste, peat, wood chips) was tested for feasibility as a component (0–30 vol.%) of a sphagnum peat container medium for growing Norway spruce (Picea abies (L.) Karst.) container seedlings in a forest-tree nursery. In proportions of up to 30% in peat, the compost additive used was shown to be a feasible material for seedling growing in forest nurseries. On average, the seedlings grew best in pure peat, but the compost additions to peat showed no marked reduction in seedling growth in greenhouses, nor were there any effect on seedling growth in the first summer after outplanting. However, a slightly elevated risk of seed non-germination and of seedling mortality was observed when the growing media contained compost in proportions of 20% or more. The compost additive in peat also changed the bulk density, structure, and chemical properties of the medium during nursery growing. The results suggest that seedling watering and fertilisation should be adjusted for each growing medium mix separately to achieve correct water, oxygen, and nutrient availability in containers during nursery growing.     

Effects of pre- and post-planting shading on growth of container Norway spruce seedlings

Norway spruce (Picea abies (L.) Karst.) is shade-tolerant and sensitive to high irradiance, summer frosts and winter desiccation, which can impair its reforestation success. In this study, artificial pre- and post-planting shading was examined to determine their effects on post-planting shoot and root growth as well as the vigor of one- and two-year-old Norway spruce seedlings. Three planting experiments were carried out on open nursery fields (Exp. 1, 2) and on a mounded forest clearcut in central Finland (Exp. 3). Before planting, the seedlings were stored over winter either in a freezer or on open fields under snow cover. For two weeks prior to planting, half of the seedlings were placed in the open and the other half under a horizontal shade netting (light transmittance 56 %) (Exp. 1, 2). All seedlings were planted with or without a vertical post-planting shade, which was located on the southern side. Post-planting shading enhanced shoot growth and reduced damage (better visual vigor and needle color and less pine-weevil damage) on Norway spruce seedlings for at least two years after planting (Exp. 2, 3). Those seedlings, that had been stored over winter in the open and kept in shade prior to planting seemed to benefit most from post-planting shading (Exp. 2). However, post-planting shading may give variable results, depending on the seedling quality and weather conditions after planting, and may even reduce shoot growth if no pre-planting shading is used (Exp. 1). Shoot growth may also be improved at the expense of root growth (Exp. 3). The costs of manufacturing and installing post-planting shades may limit their use in practice, for example, to selected regeneration sites where there is high risk of frost damage but where no alternative silvicultural procedure (shelterwood or nurse crop) has been used.