Water relations and morphological development of bare-root jack pine and white spruce seedlings: seedling establishment on a boreal cut-over site

Bare-root jack pine (Pinus banksiana Lamb.) and white spruce (Picea glauca (Moench) Voss) seedlings were planted on a boreal cut-over site and subsequent growth and seedling water relation patterns were monitored over the first growing season. Comparison of morphological development between white spruce and jack pine showed jack pine seedlings had greater new root development and a lower new shoot/new root ratio, while white spruce seedlings had greater new shoot development. Seasonal water relation patterns showed white spruce seedlings to have a greater decrease in xylem pressure potential (_x) per unit increase in transpirational flux density in comparison to jack pine seedlings. These results suggest that the greater resistance to water flow through the soil-plant-atmosphere continuum in white spruce seedlings compared to jack pine seedlings may be due to the relative lack of new root development in white spruce. Stomatal response of the seedlings showed that as absolute humidity deficit between the needles and air (AHD) increased, needle conductance (gwv) decreased in both species, but at low AHD levels white spruce had gwv approximately 35% higher than jack pine. For white spruce seedlings, gwv decreased as _x became more negative in a predictable curvilinear manner, while gwv of jack pine seedlings responded to _x with a threshold closure phenomenon at approximately - 1.75 MPa. Tissue water potential components for jack pine and white spruce seedlings at the beginning and end of the growing season showed jack pine to reach turgor loss at 76% relative water content while white spruce reached turgor loss at 88% relative water content. White spruce seedlings showed osmotic adjustment over the growing season, with an osmotic potential at turgor loss of - 1.27 MPa and - 1.92 MPa at the beginning and end of the growing season, respectively. Jack pine did not show any osmotic adjustment over the growing season. The implication of morphological development on water relation patterns are discussed with reference to successful seedling establishment.     

Differences in growth and mineral nutrition of seedlings produced from ten white spruce seed orchards

To meet the needs for improved spruce seeds in the province of Quebec, Canada, 17 first-generation white spruce seed orchards (SO) were established. These SOs are located in different bioclimatic domains and contain seed trees originating from geographically and genetically distinct sources. To evaluate the influence of SO on seedling growth and morphology, seedlings produced with seeds originating from the ten most commonly used first-generation white spruce SO in Quebec were raised under similar nursery conditions. Tissue nutrient concentrations of seedlings evolved similarly among seed orchards during the second growing season. At the end of the growing season, only shoot phosphorus concentrations were significantly different. When modeled with a logistic function, there was a significant difference between height and diameter growth curve parameters of seedlings from distinct SO during the second growing season. These differences led to significant differences in the height and shoot dry mass of the seedlings at the end of their second growing season, but not in their diameter or root dry mass. The ten SOs were clustered in two groups according to the above-ground characteristics of their progeny. This limited amount of morphological diversity suggests that expanding the size of the present seed zones may be an appropriate course of action for white spruce seed production in Quebec.     

Assessment of Root Freezing Damage of Two-year-old White Spruce,Black Spruce and Jack Pine Seedlings

Whole root systems of 2-yr-old containerized white spruce [Picea glauca (Moench) Voss], black spruce [Picea mariana (Mill.) B.S.P.] and jack pine (Pinus banksiana Lamb.) seedlings, with intact root plugs, were exposed to various frost temperatures, which a preliminary test indicated would induce approximately 0 (control), 20, 40, 60, 80 and nearly 100% frost damage. Damage to root systems was evaluated using: (1) two measures of electrolyte leakage (relative conductivity and total tissue leakage after autoclaving); (2) water loss after pressurization; (3) chlorophyll fluorescence (Fv/Fm, maximal PSII photochemical efficiency) measured 4, 21 and 30 days after the beginning of seedling regrowth and (4) live root dry mass measured 21 days after the artificial frost and 60 days after the beginning of regrowth. Seedling survival and growth after the artificial frost were evaluated using live root dry mass measured after 60 days of regrowth and new shoot length, stem diameter, and root and shoot dry mass. Live root dry mass, dead tissue leakage, jack pine root water loss and fluorescence measurements were all significantly correlated with one or more of the growth variables and the number of significant correlations varied with species. Dead tissue leakage measurements appear to be the most promising method for evaluating root damage to 2-yr-old well-developed root systems of these species.     

Heat damage in boxed white spruce (Picea glauca [Moench.] Voss) seedlings: Its pre-planting detection and effect on field performance

This study investigated the effects of holding 1+0 PSB313a white spruce (Picea glauca (Moench.) Voss) seedlings in storage boxes at air temperatures of 5, 10, 20, 30 and 40°C for 12, 24, 48, 72 and 96 h before planting. The ability to detect physiological damage to seedlings as a result of such treatment, before planting, was also examined. After one growing season, no needle damage or mortality >8% was found for temperature treatments up to 20°C for 4 days. At 30°C and above, seedling damage and mortality increased, while bud flush, shoot height, stem diameter and shoot dry weight decreased with increasing temperature and duration of treatment. Seedling mortality in the field was 100% after the 40°C treatment exposure for 72 h or longer. Pre-planting needle electrolyte leakage was indicative of visible needle damage 14 days after planting, whereas stem electrolyte leakage and root growth potential were more closely related to end of season plantation mortality. Despite the lack of damage observed at 20°C or below, preplanting exposure of white spruce seedlings to temperatures above 5°C, during transportation and field storage, is not recommended.     

Growth, allocation and tissue chemistry of Picea abies seedlings affected by nutrient supply during the second growing season

One-year-old Norway spruce (Picea abies (L.) Karst.) seedlings were grown hydroponically in a growth chamber to investigate the effects of low and high nutrient availability (LN; 0.25 mM N and HN; 2.50 mM N) on growth, biomass allocation and chemical composition of needles, stem and roots during the second growing season. Climatic conditions in the growth chamber simulated the mean growing season from May to early October in Flakaliden, northern Sweden. In the latter half of the growing season, biomass allocation changed in response to nutrient availability: increased root growth and decreased shoot growth led to higher root/shoot ratios in LN seedlings than in HN seedlings. At high nutrient availability, total biomass, especially stem biomass, increased, as did total nonstructural carbohydrate and nitrogen contents per seedling. Responses of stem chemistry to nutrient addition differed from those of adult trees of the same provenance. In HN seedlings, concentrations of alpha-cellulose, hemicellulose and lignin decreased in the secondary xylem. Our results illustrate the significance of retranslocation of stored nutrients to support new growth early in the season when root growth and nutrient uptake are still low. We conclude that nutrient availability alters allocation patterns, thereby influencing the success of 2-year-old Norway spruce seedlings at forest planting sites.     

Effects of Root Freezing on the Physiology and Growth of Picea glauca,Picea mariana and Pinus banksiana Seedlings Under Different Soil Moisture Regimes

The root systems of 2-yr-old Picea glauca, Picea mariana and Pinus banksiana seedlings were submitted to various frost temperatures during an artificial frost to induce different levels of root damage. Frost-damaged and control seedlings were placed in a greenhouse under high and low soil moisture regimes. Seedling growth and physiology were evaluated periodically. Seedling survival was reduced when root damage reached levels of 60-80%. Root systems of all three species showed partial to total recovery by the end of the experiment. In general, root freezing damage caused reductions in seedling growth, with these reductions becoming less significant over time. Root damage had little to no effect on black spruce and jack pine seedling physiology, while white spruce CO 2 uptake decreased with increasing root damage. Shoot nitrogen content of all three species decreased slightly with increasing root damage.     

Effects of the physical properties of sphagnum peat on the nursery growth of containerized picea mariana and picea glauca seedlings

Containerized black spruce (Picea mariana [Mill.] B.S.P.) and white spruce (Picea glauca [Moench] Voss) seedlings were grown from seed in Sphagnum media at two different degrees of humification (light and moderate) and at two artificially created textural grades (with or without particles < 1.3 mm). During the 26‐week growing period, the water content in the media was maintained at 60% of container capacity. At the end of the growing period, white spruce seedlings grown in the peat media enriched in fine particles (<1.3 mm) had a greater height, diameter, and root and shoot dry mass than those grown in peats deprived of fine particles. The degree of humification per se had little influence on growth. Black spruce seedlings, on the other hand, showed only a small increase in height with the addition of fine particles. Significant (p <0.05) linear relationships were found between physical properties of the media and final morphological measurements of white spruce: between easily available water and both height (R =0.97) and shoot dry weight {R =0.98), and between air volume and stem diameter (R = —0.95). Water relations parameters of black spruce and white spruce were largely unaffected by differences in the physical properties of the peat media.     

Atmospheric CO2 enrichment and soil N fertility effects on juvenile ponderosa pine: Growth,ectomycorrhizal development,and xylem water potential

Interactive effects of elevated atmospheric CO₂ and soil N fertility on above- and below-ground growth, mycorrhizal colonization, and water relations of juvenile ponderosa pine (Pinus ponderosa Dougl. ex Laws.) were investigated. One-year-old seedlings were planted in undisturbed field soil within open-top chambers which permitted creation of atmospheres with 700 μl l⁻¹, 525 μl l⁻¹, or ambient CO₂ concentrations. High and medium soil N treatments were imposed by incorporating sufficient (NH₄)₂SO₄ to increase total N by 200 μg g⁻¹ and 100 μg g⁻¹, respectively, while unamended soil, which had a total N concentration of approximately 900 μg g⁻¹, constituted the low N treatment. Following each of two consecutive field growing seasons, whole seedlings of every combination of CO₂ and N treatment were harvested to permit assessment of shoot and root growth and quantification of ectomycorrhizal development. Late in the second growing season, a simulated drought episode was imposed by withholding irrigation during which predawn and midday xylem water potential and soil water potential were measured. The initial harvest revealed that coarse and fine root weights were increased by CO₂ enrichment during the first growing season. This result was most apparent in the 525 μl l⁻¹ CO₂ treatment and high soil N, which produced the greatest root volume as well. Shoot/root ratio decreased with increasing CO₂ at the first harvest. After two growing seasons, elevated CO₂ increased seedling diameter, shoot and root volume, and shoot and coarse root weight, again most prominently in high N. Unlike the initial results, however, stimulation of seedling growth by the 700 μl l⁻¹ CO₂ atmosphere exceeded that in 525 μl l⁻¹ CO₂ after two growing seasons, and shoot/root ratio was unaffected by either CO₂ or N. At both harvests, seedlings grown in the enriched atmospheres generally had higher mycorrhizal counts and greater percentages of colonized root length, but differences among treatments in ectomycorrhizal development were nonsignficant regardless of quantification method. During the imposed drought episode, xylem water potential of seedlings grown in elevated CO₂ descended below that of seedlings grown in the ambient atmosphere as soil water potential decreased, most notably in the predawn measurements. These results suggest that CO₂ enrichment stimulates shoot and root growth of juvenile ponderosa pine under field conditions, a response somewhat dependent on soil N availability. However, below-ground growth is not increased proportionally more than that above ground, which may predispose this species to greater stress when soil water is limited.     

Inoculation of Picea abies (L.) Karst. seedlings with vegetative inocula of ectomycorrhizal fungi Suillus bovinus (L.: Fr.) O. Kuntze and Inocybe lacera (Fr.) Kumm.

Perlite-peat substrate (2:1 v:v) fumigated with Basamide was inoculated with vegetative inocula (a mixture of perlite and peat moistened with the MMN liquid medium) of ectomycorrhizal fungi Suillus bovinus (isolate TUZ 105) and Inocybe lacera (isolate X/14) immediately before seeding with Norway spruce (Picea abies [L.] Karst.) in a nursery bed. Suillus inoculum was applied at rates of 0.5; 1.0; 1.5 and 2.0 litres per m², Inocybe inoculum at rates of 0.5 and 1.5 litres per m². At the end of the first growing season, all inoculation treatments showed a significantly greater mycorrhizal infection of bareroot seedlings compared to that found in both fumigated and unfumigated controls. The ectomycorrhizal 1-year-old seedlings were transplanted into containers. At the end of the second year, ectomycorrhizal infection of the 2-year-old container-grown seedlings was considerably less than that of the 1-year-old barerooted seedlings, probably as a consequence of too high fertility and/or insufficient porosity/aeration of pure peat moss medium. There was no difference in seedling growth between inoculated and uninoculated seedlings throughout the experiment.     

Storability measures of Norway spruce and Scots pine seedlings and assessment of post-storage vitality by measuring shoot electrolyte leakage

As indoor frozen storage is increasing in forest tree nurseries it is important to have accurate methods for assessing seedling storability in autumn and methods to determine post-storage vitality. Storability of spruce (Picea abies (L.) Karst.) and pine (Pinus sylvestris L.) seedlings can be based on determination of dry matter content (DMC) of seedling shoots or by freezing shoots at –25°C and thereafter measure electrolyte leakage (SEL_diff–25). To compare these two methods we stored 1-year-old spruce and pine seedlings at different occasions during the autumn. To test if leakage of electrolytes from shoots (SEL) could indicate deteriorated vitality, we measured SEL at the end of storage. After storage seedling viability was determined in a three-week growth test, measuring shoot and root growth capacity (RGC). Determination of freezing tolerance (SEL_diff–25) before storage had a better ability to predict the outcome of storage compared to the DMC test. Measuring SEL at the end of the frozen storage period accurately indicated seedling vitality. Seedlings with SEL of 0–5% had a high survival rate whereas SEL over 10% indicated low survival and growth capacity after storage. The SEL method has a potential to become a screening test for identifying batches of seedlings that have been damaged during storage in the nursery.     

Effects of soil temperature on shoot and root growth and nutrient uptake of 5-year-old Norway spruce seedlings

Soil temperature is a main factor limiting root growth in the boreal forest. To simulate the possible soil-warming effect of future climate change, 5-year-old Norway spruce (Picea abies (L.) Karst.) seedlings were subjected to three simulated growing seasons in controlled environment rooms. The seedlings were acclimated to a soil temperature of 16 degrees C during the first (GS I) and third growing seasons (GS III), but were assigned to random soil-temperature treatments of 9, 13, 18 and 21 degrees C during the second growing season (GS II). In GS II, shoot diameter growth was lowest in the 21 degrees C treatment and root growth was lowest in the 9 degrees C treatment. In GS III, shoot height and root length growth improved in seedlings that had been kept at 9 degrees C during GS II, indicating compensatory growth in response to increased soil temperature. The temporary decrease in soil temperature had no long-lasting significant effect on seedling biomass or total nutrient uptake. At the end of GS III, fine roots of seedlings exposed to a soil temperature of 21 degrees C in GS II were distributed more evenly between the organic and mineral soil layers than roots of seedlings in the other treatments. During GS II and GS III, root growth started earlier than shoot growth, decreased during the rapid shoot elongation phase and increased again as shoot growth decreased.     

Frost damage to planted Norway spruce seedlings — influence of site preparation and seedling type

Damage to Norway spruce (Picea abies (L.) Karst.) seedlings by summer frost was monitored on 10 clear-cuttings of various ages to which slash removal and four types of site preparation had been applied. The clear-cuttings were established on two sites (5 on each) in southern Sweden from 1989 through 1993 and planted each year from the year of cutting until 1993. In total, 7680 seedlings were analysed for frost injuries during the first three years following planting. The site preparation methods evaluated were: application of herbicide to ground vegetation; mowing of ground vegetation; scarification (mounding); and control. Two seedling types, bare-rooted and containerised seedlings, were evaluated.Periods of frost susceptibility were calculated using data on bud and shoot development during 1997 together with weather data for each of the studied years and sites. The date of flushing was well correlated to the air temperature sum (+5°C threshold value) in spring. Frost damage varied considerably between sites and study years. The lowest measured minimum air temperature and the frost-day sum during the frost-susceptible period were correlated to the frequency of frost damage. Soil scarification reduced frost damage in the first growing season. Bare-rooted seedlings had a considerably lower frequency of frost injury compared with containerised ones, possibly because flushing of the former was delayed. There was no statistically significant effect of herbicide application, mowing or slash removal on the frequency of frost damage. Seedling growth was significantly reduced by frost injury, especially in cases where injuries were sustained during several years. Survival was only slightly affected by frost damage.     

Characterizing the frost sensitivity of black spruce photosynthesis during cold acclimation

We used photosynthetic light response curves to measure and model the responses of two provenances of 3-year-old black spruce (Picea mariana (Mill.) BSP) seedlings to severe artificial frost treatments applied at 2-week intervals during cold acclimation. Black spruce seedlings responded to cold acclimation with long-term suppression of photosynthetic capacity (Amax) and apparent quantum-use efficiency (alpha'). Short-term reductions in both photosynthetic parameters following frost treatments were dependent on the extent of cold acclimation of the seedlings and the severity of the frost treatments. Large reductions in Amax in response to the frost treatments were observed in seedlings that had undergone little cold acclimation and these reductions were associated with an irreversible reduction in alpha'. Such seedlings recovered only partially during the subsequent 23 days, whereas seedlings in most other treatments showed complete recovery of Amax after 13 days. The impact of frost treatments on Amax and alpha' did not vary with seedling provenance. We propose an algorithm that predicts the combined effects of cold acclimation and severe freezing temperatures on the extent of the suppression of A(max) during autumn. The algorithm is based on (1) the maximum Amax observed during the growing season, (2) the accumulation of cold degree-days, based on a minimum nocturnal temperature < 5 degrees C, and (3) the severity of freezing temperatures during autumn. The parameters developed in the algorithm showed that cold acclimation of black spruce seedlings had a greater impact on the reduction of Amax in autumn than did the severe frost treatments. Mean Amax of seedlings subjected to artificial frosts showed a strong correlation with values predicted by the algorithm (r2 = 0.91).     

Field performance of Quercus petraea seedlings grown under competitive conditions: influence of prior undercutting in the seedbed

Quercus petraea was undercut according to the following procedure: undercutting first year once (July, September, November), twice (July and November), or undercutting in two consecutive years (September of year 1 and either July, September or November of year 2). Undercutting decreased height and dry weight of the seedlings compared to uncut control seedlings. Undercutting in September and July in two consecutive years increased the number of first-order lateral roots. Field performance was evaluated by transplanting under two conditions, (a) competition with a mixture of grasses with no irrigation or fertilisation and (b) standard conditions with fertilisation and irrigation first year and no competition with grass. After two growing seasons under competitive conditions, seedlings undercut in September of year 1 had a significantly higher dry weight compared with that of uncut control seedlings. Numbers of lateral roots and field performance under competitive conditions was related when numbers of lateral roots were small, but not when high. Competitive conditions had limited effect on root growth after one growing season, whereas shoot growth was reduced. After two growing seasons both shoot and root growth were reduced in all treatments compared with standard conditions.     

Species mixing effect on Norway spruce response to elevated CO2 and climatic variables: root and radial growth response

A 7-year study was conducted to examine the growth (diameter and root) response of Norway spruce (Picea abies (L.) Karst.) seedlings to elevated CO₂ (CO_2ELV, 770 μmol (CO₂) mol^?1) in different mixture types (monospecific (M): a Norway spruce seedling surrounded by six spruce seedlings, group-admixture (G): a spruce seedling surrounded by three spruce and three European beech seedlings, single-admixture (S): a spruce seedling surrounded by six beech seedlings). After seven years of treatments, no significant effect from elevated CO₂ was found on the root dry mass (p?=?0.90) and radial growth (p?=?0.98) of Norway spruce. Neither did we find a significant interaction between [CO₂]?×?mixing treatments (p?=?0.56), i.e. there was not a significant effect of CO₂ concentrations [CO₂] in all the admixture types. On the contrary, spruce responses to admixture treatments were significant under CO_2AMB (p?=?0.05), which demonstrated that spruce mainly increased its growth (diameter and root) in M and neighbouring with beech was not favourable for spruce seedlings. In particular, spruce growth diminished when growing beside high proportions/numbers of European beech (S). Here, we also evaluated the association between tree-ring formation and climatic variables (precipitation and air temperature) in different admixture types under elevated and ambient CO₂ (CO_2AMB, 385 μmol (CO₂) mol^?1). Overall, our result suggests that spruce responses to climate factors can be affected by tree species mixing and CO₂ concentrations, i.e. the interaction between climatic variables?×?admixture types?×?[CO₂] could alter the response of spruce to climatic variables.

     

Root-freezing damage in the containerized nursery: impact on plantation sites – A review

Root-freezing damage frequently occurs in forest nurseries operating in cold climates. This type of damage arises because: (i) environmental cues for root cold acclimation differ from those for shoot acclimation; (ii) the root growing season is longer than shoot growing season; (iii) strong differences in root cold tolerance exist among species and provenances; (iv) root tissues are less frost tolerant than those of shoots, and young roots are less tolerant than mature ones; and (v) cultural practices can adversely affect root cold hardiness. To quantify root-freezing damage, different techniques have been tested. Electrolyte leakage is the most widely used and provides a good correlation with survival and regrowth. The impact of root-freezing damage on seedling performance has been studied under controlled and field conditions. Seedlings with root-freezing damage showed a reduction in survival and growth. Survival was reduced when root-freezing damage are severe. Growth reduction is mainly explained by a reduction in water and nitrogen uptake. The identification of a threshold in root-freezing damage below which survival and regrowth would not be affected should be determined for species most commonly used in reforestation. An erratum to this article is available at .     

Frost hardiness, bud phenology and growth of containerized Picea mariana seedlings grown at three nitrogen levels and three temperature regimes

We studied the influence of temperature and near- and sub- optimal mineral nutrition of black spruce seedlings (Picea mariana [Mill.] B.S.P.) during their second growing period on bud set, bud development, growth, mineral content and cold tolerance. Bud break and growth after bud break were also studied. Seedlings were grown for 106 d in growth chambers under three temperature regimes in combination with three concentrations of a fertilizer. They were then cold hardened for 56 d and dehardened for 66 d.Under these near- and sub-optimal N levels, bud formation occurred during the growing season. Bud formation was accelerated with decreasing fertilization, but was not affected by temperature treatments. Needles from seedlings with 0.64% N (dry mass basis) before hardening did not harden. Those with 0.87% N showed a lesser degree of hardiness than those with 1.28% N. Stem diameter increased at the beginning of the hardening period. During this acclimation period, shoot dry mass decreased with time at a constant rate and at the same rate over time for all treatments whereas root dry mass was more variable. Total number of needle primordia was low and no difference was observed among growing conditions. Bud break was similar in all treatments. Following bud break, shoot height and stem diameter increases were small but their magnitude varied with the nutritional regimes applied during the previous growing period. During hardening, nitrogen concentration of shoot tissues first increased and then decreased; phosphorus concentration first increased and then remained stable; potassium concentration remained stable. Concentration of these three elements generally decreased in the roots during this hardening.     

Chlorophyll fluorescence,root growth potential,and stomatal conductance as estimates of field performance potential in conifer seedlings

After cold storage, conifer seedlings in British Columbia are tested for field growth potential before planting. We compared three tests of performance potential using container-grown seedlings of Douglas-fir, interior spruce, lodgepole pine, and western larch (14 seedlots total). On several autumn dates, seedlings were lifted and stored at −2°C. The following spring we tested stored seedlings for root growth potential (RGP), chlorophyll fluorescence (CF), and stomatal conductance (Gs), and then planted seedlings in nursery beds. We assessed survival and shoot dry weight (SDW) after one growing season. Performance test results were significantly correlated with each other (r ≥ 0.47) but showed different relationships with field performance, which varied with lift date. The best performance predictor was the sum of CF and RGP (R ² = 0.79 for 78 seedlot by lift-date combinations), which minimized the risk of planting poor seedlings and not planting good seedlings. A sum of 83 for CF (Fv/Fm %) and RGP (new roots >1 cm) provided a threshold above which survival and growth were good. For evergreen conifers, Gs was a good performance predictor, but required extra time to measure leaf area. We recommend a combination of CF and RGP to assess vigor of shoot and root systems before planting. Wolfgang D. Binder––Scientist Emeritus.     

Site preparation: Water relations and growth of newly planted jack pine and white spruce

Bareroot jack pine (Pinus banksiana Lamb.) and white spruce (Picea glauca (Moench) Voss) were planted near Elliot Lake, Ontario, on a boreal reforestation site. Site preparation treatments were mixed, mineral and undisturbed (i.e., control) soil. Seedling water relations and growth were examined during the first field season. During the first 28 days after planting, jack pine base (i.e., predawn) and minimum xylem water potential readings were more negative in the control site preparation treatment. White spruce, during the first 10 days, in all site preparation treatments had base and minimum xylem water potential readings more negative than –1.7 MPa. By day 28 base xylem water potentials of white spruce had increased to approximately –1.0 MPa in all site preparation treatments. As the growing season progressed, white spruce minimum xylem water potential readings ceased exceeding the measured turgor loss point first in the mixed followed by the mineral and then control site preparation treatment. Jack pine minimum xylem water potential readings, in all site preparation treatments, almost never exceeded the measured turgor loss point. Water stress and stomatal optimization integrals, day 28 and 125, for both species showed least water stress and greater stomatal optimization in the mixed, mineral and control site preparation treatments, respectively. Both species had less new root growth in the field during the first 28 days after planting compared to seedlings grown for 28 days in a greenhouse for root growth capacity testing. Root growth at 28 days and both shoot and root development at the end of the growing season, were greatest to least in mixed, mineral, and control site preparation treatments, respectively.     

Shoot and root sensitivity of containerized black spruce,white spruce and jack pine seedlings to late fall freezing

Damage to containerized forest seedlings due to freezing can occur in the fall or early winter in Canadian forest nurseries. The following spring, damage to shoots and impairment of growth is observed. The objectives of this experiment were to measure the impact of late fall low temperatures (0° to --30°C) on whole seedlings of the three most common species used for reforestation in Quebec: black spruce (BS), white spruce (WS) and jack pine (JP). Impacts of freezing temperatures on (i) whole seedling and apical bud mortality, (ii) shoot growth and root mortality, (iii) stem electrical resistance, (iv) shoot and root water relations, (v) concentrations of N, P, K, Ca, Mg, and total sugars in shoots were assessed. JP showed the highest rate of whole seedling mortality while WS showed the highest rate of apical bud mortality. JP was the most severely affected: destruction of the root system at low temperatures as well as a reduction of shoot growth and stem diameter and a decrease (more negative) in shoot and root water potential. WS showed a reduction of shoot growth despite no apparent damage to the root system at low temperatures. BS was not affected by temperatures as low as --30°C. Nutrient and sugar concentrations were not affected by low temperature treatments.