Heat damage in tree seedlings and its prevention

Tree seedlings start to suffer stem damage or tissue death when the temperature at the soil surface reaches approximately 52°C. Seedling mortality rate accelerates as temperatures increase. Resistance to heat damage increases with size as the ability of a seedling to shade its base increase. Small newly germinated seedlings are at risk in late spring and early summer, while larger nursery-grown seedlings are at risk in mid to late summer, especially on soils with low heat capacity or conductivity, or with surfaces that are dry, dark colored or covered with organic matter. Heat damage to natural and planted seedlings usually occurs on flat or south-facing sites in regions with hot dry summers and clear skies, but can also occur in wetter regions under dry clear conditions. Shading only the basal portion of the stem appears to be as effective in preventing heat damage as shadingthe entire stem and some foliage, which can also reduce transpiration. Overhead shade and shade from live plants can reduce growth and survival.     

Establishment and growth of white spruce on a boreal forest floodplain: Interactions between microclimate and mammalian herbivory

White spruce (Picea glauca (Moench) Voss) is a dominant species in late-successional ecosystems along the Tanana River, interior Alaska, and the most important commercial timber species in these boreal floodplain forests. Whereas white spruce commonly seed in on young terraces in early primary succession, the species does not become a conspicuous component of the vegetation until after 60–80 years. To address what abiotic and/or biotic factors may explain the paucity of spruce in earlier stages of succession, we examined germination and growth of planted white spruce seedlings across an environmental gradient that included variation in soil physico-chemical properties in the presence and absence of mammal browsing. The effect of browsing pressure over the first four years after planting was most noticeable on the older terraces. Likewise, direct effects of hare browsing on spruce seedling mortality were only manifested at the oldest sites. Spruce germination and survival was inversely proportional to soil cation concentrations, which was largely controlled by temperature-driven evapotranspiration. High light intensities and high air temperatures significantly reduced seedling growth, whereas variation in soil moisture only explained a significant amount of variation in seedling survival. Temperatures within the needle clusters on terminal shoots reached values that adversely affect photosynthesis (>32 °C) on multiple occasions over the growing season. We conclude that the direct (temperature) and indirect (soil chemistry) effects of high insolation are major factors constraining spruce performance on early successional terraces, and that these effects can be significantly exacerbated by mammal browsing on associated deciduous vegetation.     

Effect of thawing regime on growth and mortality of frozen-stored Norway spruce container seedlings planted in cold and warm soil

One-year-old frozen-stored Norway spruce (Picea abies (L.) Karst.) container seedlings were planted in a controlled environment providing an air temperature of 22°C and soil temperature of 9±1 or 18±1°C. At planting the root plugs were either frozen or had been thawing for 4 days at 9°C. During a 5-week growing period, in both cold and warm soil the root growth and height growth were less in frozen-planted seedlings than in thawed seedlings. In addition, frozen-planting delayed bud burst and increased mortality. Soil temperature, however, had no effect on bud burst or mortality. Low soil temperature retarded root growth of seedlings thawed before planting but resulted in both retarded root growth and height growth if root plugs were frozen when planted. These results indicate that planting Norway spruce seedlings with frozen root plugs constitutes a considerable risk for successful forest regeneration at soil temperatures normally prevailing in Fennoscandia in spring or early summer especially if the soil is dry at the time of the planting.     

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.     

Effect of planting stocktype and cultivation treatment on the establishment of Norway spruce on cutaway peatlands

In order to determine the effect of stocktype and cultivation treatment on the field performance (survival and growth) and physiological status of Picea abies in cutaway peatlands, small bare-root, large bare-root and containerised seedlings were planted in a deep ploughed and a control site. Survival after 2 years was good across all treatment (>90%) except for the large bare-root seedlings growing in the control site (84%). For all the morphological characteristics assessed in this study, there was no significant interaction between stocktype and cultivation treatment indicating that the growth response to site cultivation was not stocktype dependent. After two growing seasons, all Norway spruce seedlings performed better in the deep ploughed site and displayed also better nutritional and physiological status. Regardless of cultivation treatment, mean height, diameter and volume increment were significantly smaller for the large bare-root seedlings while the small bare-root seedlings displayed the greatest growth rates. In order to promote early height growth in container and small bare-root stock, large diameter is important. Other initial characteristics such as foliar nitrogen content may also have a strong influence on first year field performance. The physiological status of the seedlings during the first year after outplanting was assessed using chlorophyll fluorescence (CF) measurements. CF measurements detected a higher level of stress for the large-bare root stock (low Fv/Fm). On the other hand, small bare-root stock displayed highest maximum potential photochemical activity which corresponded to greatest growth rates. Container seedlings demonstrated higher capacity for photosynthetic electron transport during the first five months after planting suggesting that they recovered from planting stress quicker and optimised better light interception and utilization than bare-root stock. It can be concluded that intensive management systems including deployment of best-adapted stocktype and site cultivation can be used to enhance early height growth of Norway spruce on cutaway peatlands.     

Relationship between tree canopy height and the production of pasture species in a silvopastoral system based on alder trees

Silvopastoral systems in New Zealand that incorporate trees planted to control soil erosion on hills largely rely on the productivity of the pastoral system for financial returns. The effect on pasture productivity of increasing the tree canopy height by pruning Italian gray alder (Alnus cordata) was investigated by measuring the response of light, soil moisture, soil temperature, pasture production of major pasture species, and grazing behaviour of sheep. A split-plot design with four replicates was used. The main plot treatments were three levels of shade (81, 23, and 12% of available photosynthetic photon flux (PPF)), created by pruning 11 year old alder grown at the same density. The sub-plot treatments were four pasture mixes: perennial ryegrass (Lolium perenne), Yorkshire fog (Holcus lanatus), and cocksfoot (Dactylis glomerata), each sown with white clover (Trifolium repens), and cocksfoot sown with lotus (Lotus pedunculatus). Soil temperature was highest under light shade. Total herbage yield at 50 mm stubble height from October to May under heavy and medium shade was 60 and 80%, respectively, of the total herbage harvested under light shade. Cocksfoot had the greatest herbage yield, either with lotus or white clover. The tillering of perennial ryegrass was suppressed by shade more than for the other grass species making ryegrass unsuitable for use in this silvopastoral system. More sheep grazed in the light shade than in the heavy shade, but there was no difference in sheep preference for cocksfoot or Yorkshire fog. Lotus was grazed more frequently than white clover. Pruning of alder to increase canopy height has the potential to improve the productivity of the understorey pasture and its acceptability to sheep.     

Density-dependent effects of northern hardwood competition on selected environmental resources and young white spruce (Picea glauca) plantation growth, mineral nutrition, and stand structural development – a 5-year study

The effects of competition from red raspberry (Rubus idaeus L.) and northern hardwood tree species on white spruce (Picea glauca (Moench) Voss) seedlings were examined on a clearcut site of the boreal mixedwood forest of the Bas-Saint-Laurent region of Quebec, Canada. A controlled experiment involving a gradient of five vegetation densities on the basis of the leaf area index (LAI) was established in a completely randomized plot design with six replications. Each of the five levels of vegetation cover (including vegetation-free plots) were examined to evaluate how they affected environmental factors (quantity and quality of light reaching the spruce seedlings, and soil temperature), spruce growth (height, basal diameter, volume index, and above-ground biomass), spruce mortality, browsing damage, spruce foliar mineral nutrition, as well as the stand structural development, during the first 5 years after seedling planting.

Each spruce growth variable analyzed in this study, according to a RMANOVA procedure, followed a negative hyperbolic form of density dependence of competitive effects. Loss of growth in young white spruce plantations in competition with northern hardwoods is likely to occur with the first few competitors. In cases where higher levels of competing vegetation were maintained over time, loss of spruce growth was extremely severe, to an extent where the exponential growth character of the young trees has been lost. At the end of the fifth year, spruce growing with no interference were larger in mean total above-ground biomass by a factor of 9.7 than those growing with the highest level of vegetation cover. Spruce did not develop a strategy of shade avoidance by increasing tree height, on the contrary. Spruce mortality differed among treatments only in the fifth year, indicating that early evaluation of spruce survival is not a strong indicator of competitive effects, when compared to diameter growth. Spruce foliar N and Ca contents were significantly reduced by the first level of competing vegetation cover, while K increased with the density of the vegetation cover, and P and Mg were not affected. Nitrogen nutrition of young white spruce planted on recently disturbed sites is discussed in relation to the potential root discrimination of this species against soil nitrate, a reaction observed by Kronzucker et al. [Kronzucker, H.J., Siddiqi, M.Y., Glass, A.D.M., 1997. Conifer root discrimination against soil nitrate and the ecology of forest succession. Nature London 385, 59–61]. The effects of hardwood competition indicate a prevalence of competition for light over a competition for nutrients, as revealed by the substantial increase in the h/d ratio of white spruce. Two indicators, h/d ratio and the quantity of light received at the tree seedling level, are suggested as a basis for the management of hardwood competition in a white spruce plantation.

Analysis of the stand structural development indicates that spruce height distribution was affected only by moderate or dense cover of vegetation, while diameter distribution, when compared to competing vegetation-free plots, was affected by the lowest level of vegetation cover. This study shows that competition influenced the stand structural development in the same way as genetic and micro-site factors by aggravating the amplitude of size inequality. The impact of hardwood competition is discussed in view of reaching an equilibrium between optimal spruce plantation growth and benefits from further silvicultural treatments, and maintaining hardwood species known to improve long term site quality, within a white spruce plantation.     

Root distribution of under-planted European beech (<Emphasis Type="Italic">Fagus sylvatica</Emphasis> L.) below the canopy of a mature Norway spruce stand as a function of light

Aboveground and belowground biomass of 15-year-old under-planted European beech seedlings (Fagus sylvatica L.) in Norway spruce stand were studied along a light gradient in three plots, in the northern part of Slovenia. Differences in soil water content, aboveground and fine root biomass distribution were confirmed between studied plots. Light had significant effect on the total biomass, root-shoot ratio (0.388 ± 0.076 under canopy, 0.549 ± 0.042 in the edge, 0.656 ± 0.047 in the open), specific root length (SRL) of fine beech roots (561.9 ± 42.2 under canopy, 664.3 ± 51.2 in the edge, 618.2 ± 72.8 in the open) and specific leaf area in beech, indicating morphological adjustment to shade. However, SRL of beech fine roots indicated no change between plots. The correlation between total aboveground and root biomass and light below the mature stand canopy was higher in the case of diffuse light intensity. Most fine roots of spruce were concentrated in the top (0–20 cm) soil layer. Beech fine roots under canopy and edge conditions were also concentrated in top (0–20 cm) soil layer and exhibited shift downwards to deeper soil horizons in open plot. Root proportion between beech and spruce changed with light toward beech with increasing light intensity for both fine and coarse roots.     

3个与杉木混植木荷种源幼苗对光照响应的差异

目的]探寻不同木荷种源混交林生产力差异的光合机制。[方法]以福建建瓯、江西信丰和浙江龙泉3个木荷代表性种源1年生和2年生幼苗为试验材料,在与杉木混植条件下,设置100%(L0)、50%(L1)和25%(L2)3种光照的光环境,研究3个木荷种源幼苗的生长性状、光合生理及叶绿素荧光特性等对不同光照响应的差异。[结果]1年生和2年生木荷幼苗的苗高、地径和干质量均表现出显著的种源差异,福建建瓯种源幼苗生长优于浙江龙泉种源和江西信丰种源。随着遮阳强度的提高,1年生和2年生2个发育阶段,福建建瓯种源幼苗比叶面积和叶绿素含量等明显增加,叶绿素a/b值、光饱和点、暗呼吸速率和Fo值等均显著降低,表现出较高的形态和生理塑性;相同遮阳处理下福建建瓯种源幼苗总叶面积、叶绿素含量和Fv/Fm值等指标显著高于浙江龙泉种源和江西信丰种源,而叶绿素a/b值、光饱和点、光补偿点和暗呼吸速率则明显低于两种源;长期遮阳和混植状态下福建建瓯种源幼苗可通过较高的生物量分配塑性,增加根系在土壤中分布来响应邻株竞争,进而促进整株干物质的积累;各光环境下,3个木荷种源2年生幼苗Fo、Fm、Fv/Fm和Fv/Fo等叶绿素荧光参数均较1年生幼苗明显升高,但各光环境间差异不显著。[结论]不同木荷种源混交林生产力差异与其对光照的塑性反应能力有关,并随幼苗年龄而变化。     

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.     

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.     

Nursery fertilization enhances survival and physiological status in Canary Island pine (<Emphasis Type="Italic">Pinus canariensis</Emphasis>) seedlings planted in a semiarid environment

We tested the hypothesis that fertilized containerized Pinus canariensis seedlings increases survival when planted in semiarid sites through the improvement of their physiological status during the establishment phase by an increment in root growth. Seedlings were cultured under two different regimes: traditional (in non-fertilized natural soil) and alternative (in fertilized peat). Morphological attributes and nitrogen content were measured before planting. Measurements of survival and growth in the plantation were made periodically for 2 years and physiological plant responses (leaf water potential, gas exchange and chlorophyll fluorescence) during the third summer after planting were tested and finally a set of plants were excavated to measure the same parameters as before planting. Seedlings cultivated using fertilized peat achieved the highest values for all of evaluated parameters. During the third dry season, big seedlings exhibited better physiological status. Therefore, enhanced root growth can result in better water uptake during the dry period thereby increasing survival and growth in the next few years after planting. A feed-back physiological model is proposed to explain P. canariensis establishment in a semiarid environment.     

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.     

Effects of soil temperature on biomass production and allocation in seedlings of four boreal tree species

One-year old seedlings of trembling aspen (Populus tremuloides Michx.), black spruce (Picea mariana (Mill.) B.S.P.), white spruce (Picea glauca (Moench) Voss), and jack pine (Pinus banksiana Lamb.) were subject to seven soil temperatures (5, 10, 15, 20, 25, 30 and 35 °C) for 4 months. All aspen seedlings, about 40% of jack pine, 20% of white spruce and black spruce survived the 35 °C treatment. The seedlings were harvested at the end of the fourth month to determine biomass and biomass allocation. It was found that soil temperature, species and interactions between soil temperature and species significantly affected root biomass, foliage biomass, stem biomass and total mass of the seedling. The relationship between biomass and soil temperature was modeled using third-order polynomials. The model showed that the optimum soil temperature for total biomass was 22.4, 19.4, 16.0 and 13.7 °C, respectively, for jack pine, aspen, black spruce and white spruce. The optimum soil temperature was higher for leaf than for root in jack pine, aspen and black spruce, but the trend was the opposite for white spruce. Among the species, aspen was the most sensitive to soil temperature: the maximum total biomass for aspen was about 7 times of the minimum value while the corresponding values were only 2.2, 2.4 and 2.3 times, respectively, for black spruce, jack pine and white spruce. Soil temperature did not significantly affect the shoot/root (S/R) ratio, root mass ratio (RMR), leaf mass ratio (LMR), or stem mass ratio (SMR) (P>0.05) with the exception of black spruce which had much higher S/R ratios at low (5 °C) and high (30 °C) soil temperatures. There were significant differences between species in all the above ratios (P<0.05). Aspen and white spruce had the smallest S/R ratio but highest RMR while black spruce had the highest S/R but lowest RMR. Jack pine had the highest LMR but lowest SMR while aspen had the smallest LMR but highest SMR. Both LMR and SMR were significantly higher for black spruce than for white spruce.     

Shade shelters increase survival and photosynthetic performance of oak transplants at abandoned fields in semi-arid climates

Forest restorations conducted in semiarid, seasonally dry climates must deal with the intense drought stress that affects tree seedlings during the dry season. Although this water deficit is the most commonly invoked source of mortality for seedlings, several other environmental factors may also preclude survival of transplants. For instance, it has been widely reported that excessive light reduces the efficiency of the photosynthetic apparatus, hence decreasing plant survival, but most seedling transplants in deforested areas are conducted under these light conditions. This study is focused in determining whether excessive light affects the photosynthetic performance and survival of Quercus coccolobifolia, a Mexican oak species, when their seedlings are transplanted in semiarid deforested areas. Further, this study tests the possibility of using artificial shade shelters to improve the ecophysiological performance and survival of seedlings. Oak seedlings were transplanted under full sunlight conditions and beneath artificial shade shelters of two different colors: white and black. To reduce water stress, and hence isolate the effects of light treatments, a drip irrigation system was implemented at each experimental plot. Seedling survival was monitored weekly for 128 days and photosynthetic performance was assessed by measuring chlorophyll fluorescence at three opportunities during the experiment. Sun-exposed seedlings showed lower photosynthetic performance and survival rates than those beneath shelters of both colors. These results suggest that sunlight damage can reduce seedling survival when they are transplanted in exposed sites, and that shade shelters can improve the success of forest restoration programs in semiarid climates.     

Tradeoff between shade adaptation and mitigation of photoinhibition in leaves of Quercus mongolica and Acer mono acclimated to deep shade

We investigated susceptibility to photoinhibition in leaves acclimated to different light regimes in intermediately shade-tolerant Japanese oak (Quercus mongolica Fisch. ex Turcz. var. crispula (Blume) Ohashi) and shade-tolerant Japanese maple (Acer mono Maxim. var. glabrum (Lév. et Van't.) Hara), to elucidate adaptability to gap formation in leaves differing in shade acclimation. We hypothesized that there is a tradeoff between shade adaptation and capacity to mitigate photoinhibition associated with leaf morphology. We simultaneously measured chlorophyll fluorescence and gas exchange in seedlings that had been grown in full sunlight (open), 10% of full sun (moderate shade) and 5% of full sun (deep shade). Shade-tolerant A. mono adapted to deep shade through changes in leaf morphology, lowering its leaf mass per area (LMA), but Q. mongolica showed little change in LMA between moderate and deep shade. Photochemical quenching (qP) did not differ between species in full sunlight and moderate shade; however, in deep shade, qP of Q. mongolica was higher than that of A. mono, suggesting that Q. mongolica grown in deep shade is less susceptible to photoinhibition at gap formation. This is consistent with the finding that chronic photoinhibition 3 days after the transfer to full sunlight, indicated by the decrease in maximum photochemical efficiency, Fv/Fm, at predawn, was less in deep-shade-grown Q. mongolica than in deep shade-grown A. mono. In deep shade, the electron transport rate (ETR) of Q. mongolica was higher than that of A. mono, whereas thermal energy dissipation through photosystem II antennae, indicated by non-photochemical quenching, was lower in Q. mongolica than in A. mono. In deep shade, the greater ETR capacity in Q. mongolica in association with higher LMA and higher leaf N content could contribute to maintaining high qP and mitigating photoinhibition. These results indicate that, by maintaining a high electron transport capacity even in deep shade, the gap-dependent and intermediate-shade-tolerant Q. mongolica trades improved shade adaptation for higher growth potential when a gap event occurs.     

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.     

Seasonal and spatial mortality patterns of holm oak seedlings in a reforested soil infected with Phytophthora cinnamomi

The viability of 1-year-old holm oak (Quercus ilex) seedlings in a soil naturally infected with Phytophthora cinnamomi was studied during 2 consecutive years in a plot located in south-western Spain. In both years, total mortality during autumn and winter was not noticeable (<2.1%). In spring, mortality levels were higher (8.3–4.6%), especially the first year. A steep increase in total mortality occurred in summer, both in the first (11.4%) and second (24.2%) year, but mortality attributable to P. cinnamomi was 1.9 and 7.6%, respectively. Thus, 2 years after planting, total cumulative mortality was 43.4%, and that attributable to P. cinnamomi 9.6% (i.e. 22.1% of total mortality). Fungus-derived mortality followed a spatially aggregated pattern in the reforestation plot, suggesting a clustered distribution of the inoculum in the soil. Furthermore, mortality by P. cinnamomi was also associated with nearness of infected adult trees in the plot. Results obtained are discussed in the framework of seasonal water deficit, P. cinnamomi damage, weed competition and sanitation techniques to be used in declined holm oak stands in Spain.     

Morphological and photosynthetic alterations in the Yellow-ipe, <Emphasis Type="Italic">Tabebuia chrysotricha</Emphasis> (Mart. Ex DC.) Standl., under nursery shading and gas exchange after being transferred to full sunlight

The objective of this study was to evaluate the effect of nursery shading on the Yellow-ipe seedling (Tabebuia chrysotricha) growth, photosynthesis, and photosynthetic acclimation after being transferred into direct sunlight. The Yellow-ipe seedlings were grown under 0, 50, 70 and 95% shade. At the 134th day of sowing, leaf gas exchange and chlorophyll were measured under current growth shading, after exposure to 15 min and two day full sunlight. With the increase of shading, the Yellow-ipe seedlings allocated more biomass to the stem and leaves and less to the roots, and there was an increase in the leaf area ratio and specific leaf area. In relation to 0% of shading there was a increase of 211% in stem, 116% in leaf, and a reduction of 200% in roots biomass when seedling were grown under 95% of shading. The total biomass accumulation had a high correlation with collar diameter (r = 0.96). More than 70% of the shading reduced the photosynthesis, and after transferring the seedlings into full sunlight, more than 50% of the shading induced a reduction in chlorophyll, stomatal conductance, photosynthesis and instantaneous carboxylation efficiency, suggesting the presence of a photoinhibition process. The Yellow-ipe seedling growth under nursery conditions should not be done under more than 50% shading, which may result in the lower seedling quality and poorer acclimation to transplantation, particularly to severe degraded areas with direct sunlight. The species can be used for recovering from totally devastated forest areas to initial recovery when full canopy are forming.     

Effects of seed water content and storage temperature on the germination parameters of white spruce, black spruce and lodgepole pine seed

The effect of seed water content (WC) (2–3, 5–6 and 22–25%, on a fresh weight basis), storage temperature (+4, −20, −80 and −196°C) and storage duration (6, 12, 24, 48 and 60 months) on the germination of white spruce (Picea glauca (Moench) Voss), black spruce (Picea mariana (Mill.) B.S.P.) and lodgepole pine (Pinus contorta Dougl. ex Loud. var. latifolia Engelm.) seed was investigated. Germination of white spruce control (untreated) seeds and seeds adjusted to 2–3% and 5–6% WC declined after 48 months of storage at −80 and −196°C, with a further decline at 60 months at −20, −80, −196°C. Germination remained high when control white spruce seeds and seeds with 2–3, 5–6% WC were stored at +4°C, over all storage durations. Generally, black spruce and lodgepole pine exhibited high germination at all storage temperatures at 2–3% and 5–6% WC as well as the control (untreated) seed, for up to 60 months in storage. Germination declined for all three species when seed was conditioned to 22–25% WC. This loss in germination was partially recovered in white spruce seed stored at +4, −20 and −80°C after storage durations of 24, 12 and 48 months, respectively, and in black spruce seeds stored at −20 and −196°C after storage durations of 24 months. Mean germination time (MGT) was relatively constant for all species, under all conditions, except for seed conditioned to 22–25% WC, where MGT increased for white spruce seed stored 48 months at −80 and −196°C, and for black spruce seed stored 24 months at +4 and −80°C and 60 months at −196°C. These results show that the optimal storage temperatures are 4°C for white spruce, and 4, −20, −80, and −196°C for black spruce and lodgepole pine, and 2–6% water content is optimal for all 3 species at these temperatures.