Planting stress in newly planted jack pine and white spruce. 1. Factors influencing water uptake

Bareroot jack pine (Pinus banksiana Lamb.) seedlings (2 + 0) and bareroot white spruce (Picea glauca (Moench) Voss) transplants (1 1/2 + 1 1/2) were taken from cold storage and planted on a clearcut forest site in northeastern Ontario on several dates between May 6 and June 5 during which period soil temperature at 15 cm depth increased from 0 to 18 degrees C. Additional cold-stored trees were transferred to a greenhouse where they were grown in pots for 0, 7 or 28 days and then placed with their roots in aerated water maintained at one of a range of constant temperatures between 0 and 22 degrees C. In both species, daytime xylem pressure potentials (Psi(x)) and needle conductances (g(wv)) decreased with decreasing soil or water temperature. At all root temperatures, g(wv) was lower, and Psi(x) higher, in jack pine than in white spruce. After 28 days in the greenhouse, g(wv) of jack pine seedlings, and Psi(x) of white spruce, was higher than in plants just removed from cold storage. In both species, water-flow resistance through the soil-plant-atmosphere continuum (RSPAC) increased as root temperature decreased. At all root temperatures, RSPAC was higher in plants just removed from cold storage than in plants grown in the greenhouse for 28 days, during which time many new unsuberized roots were formed. At root temperatures above 10 degrees C, RSPAC of both species was higher in trees newly planted in mineral soil than in trees with roots in aerated water; presumably because the roots of planted trees had limited hydraulic contact with the soil. On the day following removal from cold storage, relative plant water flow resistance increased, in both species, more rapidly with declining root temperature than could be accounted for by the change with temperature in the viscosity of water, thus indicating an effect of temperature on root permeability. The same effect was evident in jack pine seedlings, but not white spruce transplants, that had been grown for 28 days in the greenhouse after removal from cold storage.     

Carbohydrate reserve accumulation and depletion in Engelmann spruce (Picea engelmannii Parry): effects of cold storage and pre-storage CO(2) enrichment

The effects of pre-storage CO(2) enrichment on growth, non-structural carbohydrates and post-storage root growth potential of Engelmann spruce (Picea engelmannii Parry) seedlings were studied. Seedlings were grown from seed for 202 days in growth chambers with ambient (340 micro l l(-1)) or CO(2) enriched (1000 micro l l(-1)) air. Some seedlings were transferred between CO(2) treatments at 60 and 120 days. Photoperiod was reduced at 100 days to induce bud set and temperature was reduced at 180 days to promote frost hardiness development for storage at -5 degrees C for 2 or 4 months. Stored seedlings were planted in a growth chamber after thawing for one week at +5 degrees C. At 80, 120, 140 and 202 days, and at each planting time after storage, seedlings were harvested for growth measurements and analysis of starch and soluble sugar concentrations. Planted seedlings were assessed for bud break every two days and new roots > 5 mm long were counted after four weeks. Carbon dioxide enrichment increased root collar diameter and almost doubled seedling biomass, with the most obvious effects occurring after bud set. Stem height was affected only slightly and shoot/root ratios were not affected at all. Carbon dioxide enrichment increased the rate of reserve carbohydrate accumulation, but did not influence the final concentration attained before storage (accounting for 32% of seedling dry weight). Needles were the major storage organ for soluble sugars, whereas roots were the major storage organ for starch. Soluble sugars were not strongly affected by two or four months of storage, but starch was reduced by more than 50% in all plant parts. None of the CO(2) treatments had an impact on bud break or root growth potential.     

Effects of soil temperature on biomass and carbohydrate allocation in Scots pine (Pinus sylvestris) seedlings at the beginning of the growing season

We studied effects of soil temperature on shoot and root extension growth and biomass and carbohydrate allocation in Scots pine (Pinus sylvestris L.) seedlings at the beginning of the growing season. One-year-old Scots pine seedlings were grown for 9 weeks at soil temperatures of 5, 9, 13 and 17 degrees C and an air temperature of 17 degrees C. Date of bud burst, and the elongation of shoots and roots were monitored. Biomass of current and previous season roots, stem and needles was determined at 3-week intervals. Starch, sucrose, glucose, fructose, sorbitol and inositol concentrations were determined in all plant parts except new roots. The timing of both bud burst and the onset of root elongation were unaffected by soil temperature. At Week 9, height growth was reduced and root extension growth was much less at a soil temperature of 5 degrees C than at higher soil temperatures. Total seedling biomass was lowest in the 5 degrees C soil temperature treatment and highest in the 13 degrees C treatment, but there was no statistically significant difference in total biomass between seedlings grown at 13 and 17 degrees C. In response to increasing soil temperature, below-ground biomass increased markedly, resulting in a slightly higher allocation of biomass to below-ground parts. Among treatments, root length was greatest at a soil temperature of 17 degrees C. The sugar content of old roots was unaffected by soil temperature, but the sugar content of new needles increased with increasing soil temperature. The starch content of all seedling parts was lowest in seedlings grown at 17 degrees C. Otherwise, soil temperature had no effect on seedling starch content.     

Physiological Characteristics and Carbohydrate Contents of Spring-lifted Picea glauca Bareroot Seedlings Following Low-temperature Storage

This study examined the effects of low-temperature storage of white spruce [ Picea glauca (Moench) Voss] bareroot seedlings to determine whether the time between lifting and planting of spring-lifted seedlings could be extended. Seedlings were lifted from the nursery beds on May 4, 1994, and stored at- 2C (frozen storage) and 4C (cold storage) for 3, 5 and 7 weeks. Frozen storage of spring-lifted seedlings resulted in an increase in sugar levels in roots and needles that progressed with storage duration. Seedlings stored in cold storage maintained a relatively constant sugar content. Needle starch content decreased with storage duration in both frozen and cold storage. In the roots of cold-stored seedlings, starch content remained relatively constant during storage; however, in the frozen-stored seedlings, root starch levels sharply declined during the initial 3 weeks of storage. The levels of total non-structural carbohydrates (starch and sugars) decreased in both types of storage in needles, but not in roots. However, the decrease was more pronounced in the cold-stored than in the frozen-stored seedlings. Gas exchange, root growth potential and number of days to bud break were similar in frozen- and cold-stored seedlings planted in the greenhouse. However, following planting in the forest, cold-stored seedlings flushed buds earlier than did frozen-stored seedlings. The results indicate that tree nurseries could consider frozen storage of spring-lifted white spruce seedlings to facilitate lifting and planting schedules.     

Effects of cold storage and water stress on water relations and gas exchange of white spruce (Picea glauca) seedlings

To determine the effects of lifting time and storage on water-stress resistance of nursery-grown white spruce (Picea glauca (Moench) Voss) seedlings, we compared gas exchange, water relations and mortality of 3-year-old seedlings lifted in October 1991 and stored at -2 degrees C for 3 months with seedlings lifted in January 1992. The seedlings were placed in nutrient solution and subjected to -1.1 or -2.7 MPa water stress induced by polyethylene glycol 3350 for 9 days. Water stress, but not lifting time, had a significant effect on seedling net assimilation, symplastic volume and turgor loss point. In a second experiment, seedlings lifted in October 1991 were stored at -2 degrees C for 7 months and compared with seedlings lifted in May 1992. The seedlings were planted in pots, and their gas exchange and water relation parameters measured in response to gradual water stress. The results suggest that prolonged cold storage retards photosynthetic recovery of seedlings after planting. Higher rates of net assimilation in seedlings lifted in May were not directly related to their water status. Nonstomatal limitations were the primary factor influencing photosynthetic rate. We conclude that the inferior ability of cold-stored seedlings to tolerate water stress was due to poor osmotic adjustment and a lag in recovery of photosynthesis.     

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.     

Leaf water status and root system water flux of shortleaf pine (Pinus echinata Mill.) seedlings in relation to new root growth after transplanting

Water relations and root growth of shortleaf pine (Pinus echinata Mill.) were studied four weeks after seedlings from a half-sib family had been transplanted to one of three regimes of soil water availability at a root zone temperature of either 15 or 20 degrees C. About one-third of the variation in new root growth was explained by the root zone environment. The interaction between root zone temperature and soil water availability accounted for 10% of the variation in new root growth. In the most favorable root environment, new roots averaged 620 mm(2) of projected surface area. Leaf water potential increased exponentially with new root projected surface area, becoming constant at about 300 mm(2). Leaf conductance and root system water flux increased linearly with new root growth.     

沙地沙棘苗冷藏造林技术研究

为了提高半干旱区沙漠化土地的造林成活率与保存率,文章对一年生沙棘苗进行了冷藏处理和造林抚育试验。试验发现:冷藏可以延长苗木的保存期,使造林得以在春季干旱多风季节之后进行,避开了干旱与大风对苗木的危害,有效地提高造林的成活率,同时也降低了造林与抚育的成本。与常规造林相比,冷藏苗造林可以节省约50%左右的费用。试验还发现沙棘苗木在冷藏过程中,适度的温度控制以及冷藏后与造林前的常态恢复训练与苗木冷藏处理后质量的好坏有着密切的联系。训练过程中要注意保持一定的湿度,训练应该选择在阴天或阴凉处进行,避免光线直射。人工开沟深坑造林技术也是提高冷藏苗造林成活率的重要技术之一。     

Effects of soil temperature and time of decapitation on sucker initiation of intact Populus tremuloides root systems

Abstract

In a growth chamber experiment, root suckering of aspen (Populus tremuloides Michx.) was assessed in relation to timing of cutting and soil temperature. Aspen seedlings were grown in large pots for 3 years before experimentation. In a 2×2 factorial experiment, 3-year-old seedlings were cut at the end of the dormant period or after leaf flush and grown at two soil temperatures (8 or 20°C) for 39 days. Root systems were evaluated for suckering response and carbohydrate reserve status. There were no differences between the two soil temperatures and times of cut in the number of sucker buds initiated on the roots, but the number of buds that developed into suckers was much greater at 20°C. Cutting the dormant seedlings delayed suckering by nearly a week, resulting in smaller suckers at the time of harvest. However, cutting the seedlings when dormant produced almost twice the number of suckers than when cutting occurred after leaf-out. Total non-structural carbohydrates (TNC) of roots declined from 35.6% of dry weight at the end of the dormant season to 21.6% at the time of leaf-out, but there were no differences between the soil temperature and timing of cut treatments. After the 39 day growth period, root systems had 7% lower root TNC in the 20°C treatment than in the 8°C treatment, likely to support the development of the emerging suckers and higher respiration demands.     

Planted conifer seedling growth under two soil thermal regimes in high-elevation forest openings in interior British Columbia

A field trial was conducted investigating the single season growth response of 1+0 313 PSB Engelmann spruce (Picea engelmannii Parry ex Engelm.) and lodgepole pine (Pinus contorta Dougl. ex Loud.) seedlings planted into two different soil thermal regimes at three high-elevation locations spanning 200 km in the Engelmann Spruce-Subalpine Fir (ESSF) biogeoclimatic zone in the Cariboo Mountains of central British Columbia. Temperature treatments represented the extremes of soil temperature commonly found in high-elevation clear-cuts. A warm soil treatment (clear day, mid-afternoon soil temperature in mid-summer of 18 to 25 °C at –10 cm) consisting of a bare mineral soil hummock (average dimensions of 100 cm × 100 cm × 40 cm) was contrasted with a cool soil treatment (clear day, mid-afternoon soil temperature in mid-summer of 10 to 13 °C at –10 cm) comprised of organic forest floor overlying mineral soil. By the end of the growing season, seedlings of both species planted into the warm treatment generally exhibited greater root, stem, foliage, and total seedling biomass than cool treatment seedlings. Measurements of root growth at 30, 60, and 90 days after planting showed that total root number and total root length were consistently greater for warm treatment seedlings than for cool treatment seedlings. Root growth was greater from the bottom rather than from the side of the root plug for all seedlings. These results suggest that the effect of low soil temperatures on outplanted styroblock conifer seedlings is pronounced and may be limiting growth performance in high-elevation plantations in British Columbia. We recommend silvicultural treatments that secure natural regeneration, ensure that warmer microsites are always planted, and utilize seedling stocktypes able to make rapid lateral root growth into warmer surface organic horizons.     

Effects of root temperature on growth and photosynthesis in conifer seedlings during shoot elongation

Growth and gas exchange characteristics were studied in pine (Pinus sylvestris L.) and spruce (Picea abies Karst.) seedlings grown in hydroponic culture in the presence of N (50 mg l(-1)) and transferred at the start of their second growing season to tap water at 5, 8, 12, 16 or 20 degrees C (air temperature between 18-20 degrees C) for 3 weeks (pine) or 5 weeks (spruce). Root growth of both species was completely inhibited at root temperatures of 5 and 8 degrees C, but increased almost exponentially as root temperature increased. Shoot growth was maximal at 12 degrees C in both pine and spruce and decreased at low root temperatures. In both species, CO(2) uptake was decreased at low root temperatures and appeared to be influenced by the pattern of nitrogen retranslocation. In pine seedlings, as root temperature increased, an increasing proportion of the total nitrogen pool was retranslocated to the new shoot, whereas in spruce seedlings nitrogen was retranslocated to the roots. Differences in the retranslocation of nitrogen in the two species were reflected in the amount of soluble protein in needles, which at the end of the experiment increased with increasing root temperature in pine, but decreased in spruce. Our data suggest that in spruce, but not pine, CO(2) uptake was limited by the amount of Rubisco.     

Effects of simulated thaw on xylem cavitation,residual embolism,spring dieback and shoot growth in yellow birch

Yellow birch seedlings (Betula alleghaniensis Britt.) that had lost more than 90% of their stem hydraulic conductivity during ambient winter temperatures were exposed to 0 and 20 days of a simulated winter thaw followed by a 48-h freezing treatment at 0, -5, -10, -20 and -30 degrees C. After measuring freezing injury to shoots and roots, the seedlings were placed in a greenhouse where recovery of xylem conductivity and new growth were measured. Shoot xylem cavitation was measured as percent loss of hydraulic conductivity. Shoot freezing injury was assessed by electrolyte leakage (EL) and root freezing injury was assessed by EL and triphenyl tetrazolium chloride reduction. Seedlings pretreated with thaw had higher stem water contents and suffered more freezing damage to roots and shoots (at -20 and -30 degrees C, respectively) than unthawed seedlings. After 3 weeks in a greenhouse, seedlings from the 0, -5 and -10 degrees C freezing treatments showed complete recovery of xylem conductivity, with substantially increased stem water contents. Poor recovery of hydraulic conductivity was observed only in seedlings that were subjected to freezing treatments at -20 and -30 degrees C, regardless of thaw treatment. Of these embolized seedlings, however, only those not previously thawed showed recovery of hydraulic conductivity or regained stem water content after 9 weeks in the greenhouse. Shoot dieback, bud burst and length of new shoots were significantly related to the extent of stem xylem cavitation and freezing injury. We conclude that (1) the simulated winter thaw predisposed yellow birch seedlings to freezing damage in shoots and roots by dehardening tissues and increasing their water content; (2) root freezing damage in turn affected the seedlings' ability to refill embolized stem xylem, resulting in considerable residual xylem embolism after spring refilling; (3) further recovery of stem xylem conductivity was attributable to growth of new vessels; (4) and the permanent residual embolism, together with root and shoot freezing injury, caused increased dieback, bud mortality and reduced growth of new shoots.     

Soil temperature limitations on gas exchange in 1‐year‐old Pinus sylvestris (L) seedlings

Effects of soil temperature on gas exchange of Scots pine seedlings were studied to evaluate the significance of reduced gas exchange in seedlings planted in cold soils. The patterns of net photosynthesis during the 3‐week period at the two constant soil temperatures (8°C and 12°C) were quite similar but at 12°C the photosynthetic rate was higher. After U days differences were no more significant. Photosynthesis at the increasing soil temperature, from 5.5°C to 13°C, decreased for the first 18 days and then recovered up to the level of other treatments. The same patterns were found for transpiration, stomatal conductance, and photosynthetic efficiency. Xylem pressure potentials and relative resistance to water flow after 3 weeks did not differ among soil temperatures. Initiation and development of current‐year needles affected all the results of gas exchange parameters.     

Effects of forest floor planting and stock type on growth and root emergence of Pinus contorta seedlings in a cold northern cutblock

A two-year field trial was conducted to determine the growth response, and root emergence pattern of interior lodgepole pine (Pinus contorta Dougl. var. latifolia Engelm.) seedlings in response to container type and forest floor removal. Seedlings were grown in Styroblocks^TM, Copperblocks^TM, or AirBlocks^TM, and were planted directly into the undisturbed forest floor or into manually prepared planting spots where the forest floor had been scraped away to expose the mineral soil. Seedlings planted into scalped planting spots exhibited marginally but significantly (7%) greater above-ground growth rates (seedling stem volume); whereas seedlings planted into the forest floor produced significantly more (11%) new roots. There were no differences in above- or below-ground biomass. Seedlings grown in Copperblock^TM containers produced a higher proportion of roots near the top of the plug when tested at lifting, however this pattern was not observed in the field. Given that scalping is more costly than forest floor planting, and that the increased shoot growth was relatively small, we recommend that forest floor planting be considered as an alternative to manual spot scalping for sites, such as the site tested here: those with cold, but well-drained soils and where competition from other plants is not a serious problem.     

High temperature and drought stress effects on survival of Pinus ponderosa seedlings

We studied the effects of high temperature and drought on the survival, growth and water relations of seedlings of Pinus ponderosa (Dougl.) Lawson, one of few coniferous tree species that can successfully colonize drought-prone sites with high soil surface temperatures. Temperature profiles were measured with 0.07-mm thermocouples in a sparse ponderosa pine forest in northern Idaho. The soil surface and the adjacent 5 mm of air reached maximum temperatures exceeding 75 degrees C, well above the lethal temperature threshold for most plants. Air temperatures 50 mm above the soil surface (seedling needle height) rarely exceeded 45 degrees C. Pinus ponderosa seedlings that survived maintained basal stem temperatures as much as 15 degrees C lower than the surrounding air. The apparent threshold temperature at the seedling stem surface resulting in death was approximately 63 degrees C for less than 1 min. No correlation between seedling mortality and needle temperature was found, although some needles reached temperatures as high as 60 degrees C for periods of 相似文献   

Effect of nursery storage and site preparation techniques on field performance of high-elevation Pinus contorta seedlings

After five years of growth at high-elevations (∼3000 m) in Utah, container lodgepole pine (Pinus contorta Dougl. var. latifolia Engelm.) seedlings survived well (80–95%) and grew to similar heights regardless of nursery storage method and site preparation technique. Seedlings received one of three storage treatments: (1) spring-sown in the nursery, overwintered in cooler storage and outplanted in July; (2) spring-sown, overwintered in freezer storage, and outplanted in July; or (3) winter-sown, no storage, and hot-planted in late August. We outplanted seedlings at two locations that were clearcut and had received two treatments of surface organic matter (coarse wood, logging slash, and forest floor) removal: surface organic matter (OM) piled with a bulldozer and burned or surface OM remaining in situ. Compared to adjacent uncut stands, both site preparation treatments increased total soil bulk density, but retaining surface OM in situ maintained soil OM, carbon, and nitrogen levels. After one growing season, seedlings planted where surface OM had been bulldozed were taller and had more biomass, although survival was similar (≥96%) across site preparation treatments. The height growth advantage disappeared after five growing seasons and although overall survival was good, survival was highest where site preparation involved removal of surface OM and freezer-stored seedlings were planted. Total non-structural carbohydrates tended to be higher in roots than in shoots and were also higher in hot-planted seedlings than in stored seedlings. Our results indicate that nursery and forest managers have several options for successful nursery production and outplanting of container lodgepole pine seedlings in the central Rocky Mountains. Using hot-planted seedlings allows for a faster turnaround time (from seed to plantable seedling) and maintaining surface OM may be a cost-effective alternative to dozer piling and burning.     

Growth of Eucalyptus marginata (Jarrah) seedlings in a greenhouse in response to shade and soil temperature

The effects of shade and soil temperature on growth of Eucalyptus marginata Donn ex Sm (jarrah) seedlings were studied in greenhouse experiments. Plant dry weight and that of all plant parts declined in response to shade, as did root/shoot ratio. Plant leaf area was less in unshaded plants than in plants grown in shade, and specific leaf area increased with shade. Unshaded seedlings had a higher light-saturated rate of photosynthesis, a higher light compensation point and a higher light saturation point than seedlings grown in 70% shade. The relationship between plant dry weight and leaf dry weight was independent of shading, whereas the relationship between plant dry weight and plant leaf area was dependent on shading. Therefore, leaf dry weight may be a better predictor of biomass production than leaf area in forest stands where shade is likely to affect growth significantly. Soil temperature had a significant effect on the growth of all plant parts except cotyledons. Total plant growth and shoot growth were maximal at a soil temperature of 30 degrees C, but root growth had a slightly lower temperature optimum such that the root/shoot ratio was highest at 20 degrees C. Roots grown at 15 degrees C were about 30% shorter per unit of dry weight than roots grown at 20 to 35 degrees C. We conclude that increases in irradiance and soil temperature as a result of overstory removal in the forest will cause significant increases in growth of E. marginata seedlings, but these increases represent a relatively small component of the growth response to overstory removal.     

Structural root growth of young Veronese poplars on erodible slopes in the southern North Island,New Zealand

In New Zealand poplars are commonly planted on moist, unstable pastoral hill country to prevent or reduce soil erosion, thereby maintaining hillslope integrity and pasture production. Mechanical reinforcement by poplar root systems aids slope stabilisation. Root mass and distribution were determined for three Populus deltoides × nigra ‘Veronese’ trees aged 5, 7 and 9.5 year planted as 3 m poles at 8 m × 8 m spacing on a hillslope near Palmerston North in the southern North Island. Most of the structural roots (≥2 mm diameter) were distributed in the top 40 cm of soil. Vertical roots penetrated to about 1.0 m, being the depth of the soil above a fragipan. Total structural root dry masses (excluding root crown) were 0.57, 7.8 and 17.90 kg for the trees aged 5, 7 and 9.5 year, respectively. Total structural root length was 79.4 m for the 5 year tree and 663.5 m for the 9.5 year tree. Surrounding trees were estimated to increase root mass density to 3 times and root length density to 4–5 times the contribution of the single tree at 9.5 year. The study indicated that root development of wide-spaced poplar trees on hillslopes was minimal in the first 5 years but then increased rapidly. These results suggest that poplar trees established from poles may take at least 5 years to develop a structural root network that will effectively bind soil.     

Soil temperature and plant growth stage influence nitrogen uptake and amino acid concentration of apple during early spring growth

In spring, nitrogen (N) uptake by apple roots begins about 3 weeks after bud break. We used 1-year-old 'Fuji' Malus domestica Borkh on M26 bare-root apple trees to determine whether the onset of N uptake in spring is dependent solely on the growth stage of the plant or is a function of soil temperature. Five times during early season growth, N uptake and total amino acid concentration were measured in trees growing at aboveground day/night temperatures of 23/15 degrees C and belowground temperatures of 8, 12, 16 or 20 degrees C. We used (15NH4)(15NO3) to measure total N uptake and rate of uptake and found that both were significantly influenced by both soil temperature and plant growth stage. Rate of uptake of 15N increased with increasing soil temperature and changed with plant growth stage. Before bud break, 15N was not detected in trees growing in the 8 degrees C soil treatment, whereas 15N uptake increased with increasing soil temperatures between 12 and 20 degrees C. Ten days after bud break, 15N was still not detected in trees growing in the 8 degrees C soil treatment, although total 15N uptake and uptake rate continued to increase with increasing soil temperatures between 12 and 20 degrees C. Twenty-one days after bud break, trees in all temperature treatments were able to acquire 15N from the soil, although the amount of uptake increased with increasing soil temperature. Distribution of 15N in trees changed as plants grew. Most of the 15N absorbed by trees before bud break (approximately 5% of 15N supplied per tree) remained in the roots. Forty-six days after bud break, approximately one-third of the 15N absorbed by the trees in the 12-20 degrees C soil temperature treatments remained in the roots, whereas the shank, stem and new growth contained about two-thirds of the 15N taken up by the roots. Total amino acid concentration and distribution of amino acids in trees changed with plant growth stage, but only the amino acid concentration in new growth and roots was affected by soil temperature. We conclude that a combination of low soil temperature and plant developmental stage influences the ability of apple trees to take up and use N from the soil in the spring. Thus, early fertilizer application in the spring when soil temperatures are low or when the aboveground portion of the tree is not actively growing may be ineffective in promoting N uptake.     

Influence of different nursery container media on rooting of Scots pine and silver birch seedlings after transplanting

Scots pine (Pinus sylvestris L.) and silver birch (Betula pendula Roth.) seedlings were grown in containers filled with growth media based on medium-textured sphagnum peat, coarse perlite and fine sand. The seedlings were then planted into fine and coarse sandy soils in 2.2 l pots, which were subjected to two water-content treatments (only one for birch). After the seedlings had grown five weeks in a greenhouse, rooting into the surrounding soil and shoot growth were measured. Addition of perlite and sand to peat medium slightly affected rooting; thus suggesting minor effects on seedling establishment. However, nitrogen concentration of the seedlings varied between growth media and correlated positively with rooting into the soil. The particle size and water content of the soil affected considerably rooting of the seedlings. Seedling height at the time of planting did not affect rooting or shoot growth. The fact that the fewest out-grown roots occurred in the dry fine sandy soil, suggests that dry soil together with high strength and resistance to root penetration reduce rooting and water uptake by container seedlings most and may thus cause water and nutrient stresses to seedlings after outplanting.