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1.
Saur E  Nambiar EK  Fife DN 《Tree physiology》2000,20(16):1105-1112
We measured patterns of change in concentrations and contents of nitrogen, phosphorus, potassium, magnesium and calcium in fully expanded leaves of young Eucalyptus globulus (Labill.) trees growing in a plantation in southeastern Australia, over a 12-month period beginning at the onset of spring. There was significant net retranslocation of mobile nutrients on a seasonal basis from green leaves, coinciding with continued growth and production of foliage. There was a close positive relationship between initial nutrient content (N, P and K) of the leaf and amount retranslocated, and a tight coupling between N and P retranslocated from leaves. Net retranslocation was significantly correlated with basal area growth increments. Artificial shading of leaves resulted in senescence and reduction in leaf mass. It also induced retranslocation of N, P and K from leaves of different ages and from different position in the canopy. Although the mechanisms underlying the effects of shading intensity on these changes were not elucidated, shading provided an experimental tool for studying retranslocation. Comparison of the results with published data for Pinus radiata (D. Don) grown in the same environment indicated a similarity between the species in patterns of change in foliar nutrient contents and in factors governing foliar nutrient retranslocation, giving rise to unifying principles.  相似文献   

2.
Studies of nitrogen (N) use by plants have confirmed some winter N uptake; however, the mode of regulation of plant N use in winter is unknown. The regulation of N use by plants during winter may differ from that in the growing season, as plant growth strongly affects N use. We investigated the effects of winter buds on winter N use by Japanese red pine (Pinus densiflora), as a previous study demonstrated that N absorbed during winter contributes significantly to leaf growth in the following spring. We conducted a bud pruning experiment during winter to examine the effects of winter buds on winter N uptake and allocation among plant organs using 15N labeling. Over a three-week labeling period, the 15N content in roots increased to 0.20 ± 0.12 mg N g DW?1, which is equivalent to 1.8 ± 1.1 % of the total N content in the roots. However, this absorbed 15N rarely appeared in needles and buds. Bud pruning did not affect 15N uptake and allocation. On the other hand, significant total N retranslocation was found within the crowns of saplings without bud pruning, but N was not retranslocated in bud-pruned plants. The bud pruning experiment indicated that N was retranslocated from needles into winter buds. Since soil N availability changes dramatically and is unstable in many forest ecosystems, N contained in needles would be a more stable source of N than newly absorbed N.  相似文献   

3.
Ueda MU 《Tree physiology》2012,32(7):859-866
Nitrogen (N) retranslocation within tree canopies has been intensively studied and assumed to function as a one-way process (e.g., from older to newer leaves). However, recent studies have found that both N output and input occur in individual leaves, suggesting that 'gross' N retranslocation exists behind 'net' N retranslocation. In the present study, the amount and direction of gross N retranslocation within a canopy of deciduous oak Quercus serrata Thunb. ex. Murray saplings were investigated. Labeling was conducted with leaves of Q. serrata saplings cultivated under conditions of low-N (LN) or high-N (HN) fertility. Subsequently, N movement within the canopy was traced. Leaves at two different positions in the canopy (top and lateral) were labeled to determine the direction of gross N retranslocation. To detect seasonal differences, the leaf-labeling experiment was conducted twice during the early and late phases of the growing season. In addition, to compare the quantitative importance of gross N retranslocation and root N uptake, the latter was determined by labeling Q. serrata roots. The N-labeling experiment revealed gross N retranslocation among leaves, i.e., from top to lateral, lateral to top and lateral to lateral positions. Gross N retranslocation was quantitatively more important than root uptake, especially for plants cultivated at LN fertility. Season also affected the amount of gross N retranslocation, and these effects differed between LN and HN fertilities. These findings suggest that N allocation within a canopy is controlled dynamically by both gross N output and input. The mechanisms controlling gross N output and input likely function as key determinants of N allocation within a tree canopy.  相似文献   

4.
Allocation of biomass and nutrients to shoots and roots was followed for three years in fast and slow growing populations of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco), a fast growing pioneer species, and amabilis fir (Abies amabilis Dougl. ex J. Forbes), a slow growing shade-tolerant species. Seedlings were grown for three seasons in five nutrient treatments containing varying proportions of nitrogen and phosphorus (N:P). In both species, growth was greatest in the 250:20 N:P treatment followed by the 100:60 and 100:20 treatments. Vector analysis showed that, in both species, relative to the 100:20 treatment, seedlings in the 20:20 treatment were N deficient and seedlings in the 100:4 treatment were P deficient, i.e., where deficiency is defined to mean that an increase in nutrient supply increases nutrient content, nutrient concentration and plant dry weight. Seedlings in the 100:60 treatment had a higher P content than seedlings in the 100:20 treatment but the same dry weight, indicative of what Timmer and Armstrong (1987) termed luxury consumption. No nutrient retranslocation was observed in either species until the third growing season. In Douglas-fir, the greatest percentage of nutrients was exported from one-year-old shoots between May and July of the third growing season to support new growth. The total amount and percent of nutrients retranslocated was higher in Douglas-fir than in amabilis fir. Amabilis fir seedlings also exported N and P from older shoots, but this was later partially replenished. In both species, P retranslocation was greatest in treatments with a high N:P ratio. Nitrogen retranslocation was greatest in amabilis fir seedlings in treatments with a low N:P ratio, and greatest in Douglas-fir seedlings in the 250:20 and 100:60 treatments. Potassium retranslocation was correlated with seedling size. Douglas-fir retranslocated more of its shoot N reserves into new growth at the expense of older needles when soil fertility was high and sinks were strong. Otherwise, both species preferentially translocated the elements in short supply. Thus, retranslocation varied with the ecological characteristics of species, the relative availability of soil nutrients and sink strength.  相似文献   

5.
Budget studies have shown that internal cycling may contribute a large proportion of the annual nutrient supply required to support new growth in trees. Use of budgets to quantify internal cycling only quantifies the net transfer of nutrients within the plant. Differential partitioning of remobilized nutrients and current nutrient uptake could lead to errors in the interpretation of results from these studies. We have quantified the dynamic relationships among tree growth, nutrient uptake and internal cycling by labeling the current uptake of N in trees that received contrasting amounts of nutrient. Two-year-old seedlings of Sitka spruce (Picea sitchensis (Bong.) Carr.) were grown in sand culture in a greenhouse for one year. The trees received nutrients in a balanced solution at either a high (high-RAR) or a low (low-RAR) relative addition rate throughout the experiment. Current N uptake was labeled with (15)N from April 13 to July 25. Thereafter, trees were re-potted in clean sand and unlabeled N applied until November 13. Overall growth was sustained for approximately 10 weeks before treatment effects were observed. Initially, no differences in the partition of growth or remobilized N occurred, although partition of current uptake favored the roots of plants in the low-RAR treatment. After 6 weeks, the partition of both growth and remobilized N altered in favor of roots of plants in the low-RAR treatment. Nutrient supply had no effect on the amount or rate of N remobilization. No evidence was found to suggest that N taken up in the current season and partitioned to preexisting shoots or roots is remobilized late in the season to support growth of new shoots. However, some trees in the high-RAR treatment exhibited a second flush of growth later in the season that was partially sustained by remobilization of (15)N from current shoots formed earlier in the season. Use of (15)N demonstrated differential partitioning of current uptake and remobilized N. The results highlight the limitations of simple budget studies for quantifying internal cycling.  相似文献   

6.
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.  相似文献   

7.
The effectiveness of spraying foliage with urea to provide nitrogen (N) to augment the seasonal internal cycling of N in young nectarine trees (Prunus persica (L.) Batsch var. nectarina (Ait. f. Maxim.), cv. Stark Red Gold) was studied. One-year-old trees were grown with contrasting N supplies during the summer and foliage was sprayed with a 2% urea solution labeled with (15)N just before leaf senescence started. After leaf abscission had finished, the trees were repotted in sand and given no further N. Remobilization of both labeled and unlabeled N for leaf growth the following spring was quantified. Leaves absorbed between 58 and 69% of the (15)N intercepted by the canopy irrespective of tree N status. During leaf senescence, the majority of (15)N was withdrawn from the leaves into the shoot and roots. Remobilization of (15)N the following spring was also unaffected by tree N status. About 38-46% of (15)N in the trees was recovered in the new growth. More unlabeled N (derived from root uptake) was remobilized for leaf growth in the spring than was withdrawn from leaves during canopy senescence the previous autumn. Therefore, soil-applied N augmented N storage pools directly, and contributed more to N remobilization the following spring than did foliar-absorbed (15)N.  相似文献   

8.
Cycling of soluble non-protein N compounds is thought to be indicative of the N-nutritional status of trees. We determined the major N forms in bark, wood and foliage and estimated the dependence of prevalent N forms on N availability in Pinus sylvestris L. trees from northern Sweden. Trees subjected to severe N limitation and trees that had been fertilized with an average 64 kg N ha(-1) year(-1) for 25 years were analyzed. Bark and wood samples were collected by tangentially cryo-sectioning the trunk into 30-microm thick sections, from the bark to the functional xylem. Soluble amino compounds were extracted from the sections for analysis. Sap samples from twigs were obtained by centrifugation, and bark samples from twigs were obtained by tissue extraction. In both needles and bark, arginine dominated the amino-N pool. Because arginine concentrations in needles increased with N fertilization, arginine dominance of the amino-N pool in needles was higher in N-fertilized trees than in control trees. In bark, N fertilization resulted in a large increase in glutamine concentration, so that glutamine accounted for a larger proportion of the amino-N pool in bark in N-fertilized trees than in control trees. Glutamine dominated the amino-N pool in wood of control trees. Nitrogen fertilization resulted in an increased proportion of arginine in the wood amino-N pool. We conclude that the composition of the amino-N pools in bark, wood and foliage is highly sensitive to N supply. The composition of the amino-N pools can contribute to the regulation of tree N-nutritional status, which is mediated by shoot to root signalling by long-distance transport of amino compounds.  相似文献   

9.
Rufat J  DeJong TM 《Tree physiology》2001,21(15):1133-1140
The PEACH computer simulation model of reproductive and vegetative growth of peach trees (Grossman and DeJong 1994) was adapted to estimate seasonal nitrogen (N) dynamics in organs of mature peach (Prunus persica (L.) Batsch cv. O'Henry) trees grown with high and low soil N availability. Seasonal N accumulation patterns of fruits, leaves, stems, branches, trunk and roots of mature, cropping peach trees were modeled by combining model predictions of organ dry mass accumulation from the PEACH model with measured seasonal organ N concentrations of trees that had been fertilized with either zero or 200 kg N ha(-1) in April. The results provided a comparison of the N use of perennial and annual organs during the growing season for trees growing under both low and high N availability. Nitrogen fertilization increased tree N content by increasing organ dry masses and N concentrations during the fruit growing season. Dry mass of current-year vegetative growth was most affected by N fertilization. Whole-tree N content of fertilized trees was almost twice that of non-fertilized trees. Although N use was higher in fertilized trees, calculated seasonal N accumulation patterns were similar for trees in both treatments. Annual organs exhibited greater responses to N fertilization than perennial organs. Estimated mean daily N use per tree remained nearly constant from 40 days after anthesis to harvest. The calculations indicated that fertilized trees accumulated about 1 g N tree(-1) day(-1), twice that accumulated by non-fertilized trees. Daily N use by the fertilized orchard was calculated to be approximately 1 kg N ha(-1), whereas it was approximately 0.5 kg N ha(-1) for the non-fertilized trees. During the first 25-30 days of the growing season, all N use by growing tissues was apparently supplied by storage organs. Nitrogen release from storage organs for current growth continued until about 75 days after anthesis in both N treatments.  相似文献   

10.
Seasonal changes in above ground dry-matter, nitrogen (N), and phosphorus (P) accumulation were measured following application of N and P in autumn or spring to 1-year-old Pinus radiata (D. Don). Dry-matter production and nutrient accumulation were measured eight times over two years following fertilization.

All trees produced dry-matter throughout the year, but during the summer, fertilized trees produced more dry-matter than unfertilized trees. In contrast to dry-matter production, nutrient accumulation showed a distinctly seasonal pattern with maximum accumulation of N and P occurring in winter and spring, when rainfall and soil moisture were highest. Accumulation of N and P either slowed markedly or ceased during summer depending on fertilizer treatment. Continued dry-matter production during summer, when nutrient accumulation was low, resulted in the decline of N and P concentrations in needles, branches and stems of all trees. This indicated that nutrients required for new growth during summer were mobilized from existing foliage and wood. Fertilization increased the concentrations of N and P in foliage and wood, and these higher concentrations persisted through summer. Spring fertilization increased N accumulation to a greater extent than autumn fertilization, this effect lasting two years. The greater dry-matter production by fertilized trees during summer indicated that growth during summer was limited by nutrient supply.  相似文献   


11.
Soil nitrogen can alter storage and remobilization of carbon and nitrogen in forest trees and affect growth responses to elevated carbon dioxide concentration ([CO(2)]). We investigated these effects in oak saplings (Quercus robur L.) exposed for two years to ambient or twice ambient [CO(2)] in combination with low- (LN, 0.6 mmol N l(-1)) or high-nitrogen (HN, 6.1 mmol N l(-1)) fertilization. Autumn N retranslocation efficiency from senescing leaves was less in HN saplings than in LN saplings, but about 15% of sapling N was lost to the litter. During the dormant season, nonstructural carbohydrates made up 20 to 30% of the dry mass of perennial organs. Starch was stored mainly in large roots where it represented 35-46% of dry mass. Accumulation of starch increased in large roots in response to LN but was unaffected by elevated [CO(2)]. The HN treatment resulted in high concentrations of N-soluble compounds, and this effect was reduced by elevated [CO(2)], which decreased soluble protein N (-17%) and amino acid N (-37%) concentrations in the HN saplings. Carbon and N reserves were labeled with (13)C and (15)N, respectively, at the end of the first year. In the second year, about 20% of labeled C and 50% of labeled N was remobilized for spring growth in all treatments. At the end of leaf expansion, 50-60% of C in HN saplings originated from assimilation versus only 10-20% in LN saplings. In HN saplings only, N uptake occurred, and some newly assimilated N was allocated to new shoots. Through effects on the C and N content of perennial organs, elevated [CO(2)] and HN increased remobilization capacity, thereby supporting multiple shoot flushes, which increased leaf area and subsequent C acquisition in a positive feedback loop.  相似文献   

12.
Three-year-old clonal cuttings of Picea sitchensis (Bong.) Carr. were grown for two years (1988-1989) in sand irrigated with a nutrient solution containing either 1.0 mol N m(-3) (low N) or 6.0 mol N m(-3) (high N) NH(4)NO(3). In 1988, all the N provided was enriched with (15)N to 4.95 atom % (labeled N). In 1989, N was supplied with (15)N at natural abundance (unlabeled N). The recovery of unlabeled and labeled N in new foliage was used to quantify the internal cycling of N. In the high-N treatment, trees had two flushes of shoot growth and a period of rapid root growth, which coincided with the second flush of shoot growth in August. The timing of root growth and the first flush of shoot growth was similar in the low-N treatment, but there was no second flush of shoot growth and a greater proportion of biomass was recovered in roots. By November 1989, the root/needle dry matter ratio was 1.95 for the low-N trees and 1.36 for the high-N trees. Nitrogen was stored overwinter in roots and current-year needles. During the first six weeks of growth in the spring of 1989, stored N was remobilized for new foliage growth. Subsequent growth depended on root uptake of N. Remobilization of stored N was apparently not affected by the current N supply, because the amount of unlabeled N recovered in foliage produced in 1988 was the same for both N treatments. During 1989, the proportion of (15)N remobilized from roots relative to that from leaves produced in 1988 was greater in low-N trees than in high-N trees. In the autumn of both years, there was rapid uptake of N into roots and current-year needles. The effects of N supply on tree growth and nitrogen use efficiency are discussed in terms of the capacity for both N storage and internal cycling.  相似文献   

13.
Nitrogen cycling was studied for four years (1983–1987) in an N-deficient 10-year-old stand of Pinus radiata growing on a yellow podzolic soil which had a low water-holding capacity. Trees were subjected to combinations of irrigation of N-fertilization resulting in a wide range of N uptake and tree growth. Net mineralization, plant uptake and leaching of soil N was monitored using a sequential coring and in-situ incubation technique. Nitrogen concentrations were measuredd monthly in live needles and litterfall. Average rates of weight loss and release of N from decomposing litter were estimated over a 3-year period using a budgeting approach.

Trees responded only to N (not to P, and there was no N×P interaction), but there was a large positive interaction between N supply and water availability. Response to fertilizer averaged + 24% over a 4-year period, but was zero during a growing-season which contained a 4-month drought. Irrigation alone increased growth by 60%, but in combination with high N availability growth increased 2–3 fold. Annual uptake of N ranged from <10 (irrigated plots in years 2 and 3 after enhanced mineralization during the initial year) to 166 kg ha−1 (during a wet growing season following heavy N fertilization). Although soil mineral-N concentrations were elevated for only about 1 year after fertilization, fertilization enhanced rates of N mineralization throughout the soil N mineralization may have resulted from re-mineralization of the large quantity (147 kg soil N mineralization may have resulted from re-mineralization of the large quantity (147 kg ha−1) of fertilizer N immobilized by the soil during the initial 8 months after fertilization, or the N released from decomposition of fine roots having higher N content. Nitrification was negligible in unfertilized soils, but increased markedly 50–100 days after fertilization and resulted in the leaching of about 60 kg N ha−1 during autumn and winter of the first year after fertilization. Fertilized soils have continued to nitrify readily. Irrigation increased rates of weight loss and N release from decomposing litter.

The rate of N uptake by trees markedly affected the concentrations of N in newly emerging and older needles, and the concentration of N in needlefall. The weighted mean concentration of N in annual needlefall ranged from 0.42% in the irrigated-only plot (most N-stressed) to 0.94% in the heavily fertilized plot during the first year after treatment. These weighted concentrations are a useful index of N uptake from the soil and of growth rate where water supply is not limiting. Except for the initial year after heavy N fertilization, annual uptake of N was equivalent to annual soil N mineralization, and N uptake was positively linearly correlated with annual basal-area increment of trees.  相似文献   


14.
Seasonal changes in concentrations of total nitrogen, free amino acids, chlorophyll, starch and sugar were measured in foliage from fertilized and unfertilized conifer forests in New Mexico and Oregon. In the New Mexico Douglas-fir (Pseudotsuga menziesii var glauca (Beissn.) Franco) forest, fertilization resulted in elevated foliar nitrogen concentrations on all dates, from an average of 9 mg g(-1) in unfertilized trees to 14 mg g(-1) in fertilized trees. In the Oregon western hemlock (Tsuga heterophylla (Raf.) Sarg.) forest, fertilization increased total N by only 15%, from 13 mg g(-1) in unfertilized trees to 15 mg g(-1) in fertilized trees. Foliar nitrogen concentrations on a weight basis were lowest in winter and spring, but did not vary seasonally when expressed on a leaf area basis. Chlorophyll concentrations increased with fertilization and had greater seasonal variation than did total nitrogen concentrations. Chlorophyll concentrations were significantly higher during the growing season than in the winter and spring months. Fertilization did not result in major changes in the proportion of total nitrogen in chlorophyll at either the Oregon or the New Mexico site. Concentrations of free amino acids varied with date and fertilization treatment; in New Mexico, amino acids were highest in the winter sample, whereas in Oregon, they were lowest in winter and spring. At both sites, amino acid concentrations were significantly higher in fertilized trees than in control trees on most dates and the ratios of amino acid-N to total N were also significantly higher in fertilized trees. For both sites, starch concentrations were nearly zero for most of the year, but increased sharply just before bud break and initiation of new growth in the spring. Although fertilization resulted in increased nitrogen concentrations in foliage at both sites, the response in New Mexico was much greater than in Oregon. These results are in agreement with forest productivity data that suggest that growth in the New Mexico site is limited by nitrogen, whereas in the Oregon site it is not.  相似文献   

15.
Seedlings of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) and western red cedar (Thuja plicata J. Donn ex D. Don) were grown at high (250 mg l(-1)) and low (20 mg l(-1)) nitrogen (N) supply for a year. Before the second growing season, half of the seedlings in each nutrient treatment were allocated to the other treatment. Half of the seedlings in each nutrient treatment then had all growing points removed. Biomass and N, phosphorus (P) and potassium (K) concentrations of old and new shoots and roots were measured three times in the second year to test the interaction of current-year and previous-year nutrient supply on biomass and nutrient allocation in these two species with different growth habits. Pruned seedlings served as controls. Unpruned seedlings of both species increased in height throughout the second growing season, except for Douglas-fir in the N250 --> N20 treatment. Repeated pruning did not prevent new shoot growth, but resulted in a 12 to 52% reduction in biomass of new shoots and new and old roots. Seedlings receiving a low N supply in the first growing season were more severely affected by pruning than seedings receiving a high N supply. Growth was reduced more by pruning in western red cedar than in Douglas-fir. Concentrations of N, P and K were higher in pruned seedlings than in unpruned seedlings. Although dry weights of all plant parts in all treatments increased throughout the second growing season, some retranslocation of N, P and K was observed from old shoots of both species in the N250 --> N20 and N20 --> N20 treatments after August. Quantities of N, P and K retranslocated were greatest in seedlings grown the previous year in the high-N treatment.  相似文献   

16.
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.  相似文献   

17.
Five soil treatments in a 4-year-old clearcut in southern Sweden affected biomass increase and net nitrogen uptake by planted Norway spruce (Picea abies (L.) Karst.) seedlings through their on net mineralisation and root growth. The patch soil treatments studied were: (i) soil inversion in an old clearcut; (ii) mineral soil from the clearcut remaining, (iii) mineral soil from the clearcut with fertiliser application during the first season; (iv) mineral soil from a nearby uncut forest replacing the clearcut mineral soil; and (v) an untreated control. Growth increased in seedlings in treatments (i) and (iii), but growth in soil treatments with humus removal was not better than that of seedlings in untreated soil. High N uptake early in the first growing season resulted in increased growth during this season in contrast to late N uptake that resulted in a high N concentration in the seedlings after the first growing season. This in turn led to a high growth rate during the next growing season. Generally, both root growth and net N mineralisation were positively correlated to N uptake in the soil treatments. Therefore, a combination of low net N mineralisation and poor root growth as a result of high soil density appears to explain the low N uptake in seedlings in undisturbed soil. The importance of competition with field vegetation for N and water was not clear. Net mineralisation was larger in soil treatments where the humus layer was retained than where it was removed. Net N mineralisation in soil from old clearcuts was the same as in soil from fresh clearcuts.  相似文献   

18.
Potassium (K) and magnesium (Mg) are essential macro-nutrients, but little is known about how they are cycled within plants. Stable isotope studies have shown that the internal cycling of nitrogen (N) is independent of current nutrient supply in temperate tree species. This is ecologically significant because it allows trees to produce rapid shoot growth in spring independent of current soil N uptake. We used stable isotopes to quantify N, K and Mg in new shoots of Sitka spruce (Picea sitchensis (Bong.) Carr.) seedlings and to compare the relative contributions from current uptake and internal cycling. Two-year-old Sitka spruce seedlings were labeled with (15)N, (41)K and (26)Mg in an abundant or a limited supply for one growing season. The trees were repotted in the subsequent dormant season to prevent further root uptake of enriched isotopes and provided with an abundant or a limited supply of unlabeled nutrients until they were harvested in early summer of the following year. The supply was switched for half the trees in the second year to create four nutrient regimes. Enrichment of (15)N, (41)K and (26)Mg in current-year growth was attributed to internally cycled N, K and Mg uptake from the previous year. The internal cycling of N, K and Mg in new growth was significantly affected by the first-year nutrient treatments. The second-year nutrient supply affected the growth rates of the trees, but had no effect on the amounts of N, K or Mg contributed from internal cycling. Thus, internal cycling of K and Mg in Sitka spruce are, like that of N, independent of current nutrient supply.  相似文献   

19.
Seasonal changes in the N and P content of foliage in a young forest of Fagus sylvatica were measured. Leaves from branches of the upper and lower crown of dominant trees and from suppressed trees were compared. Nutrient retranslocation rates during senescence differed considerably between trees. This variation appeared not to be related to any differences in environmental factors or tree vigour, and was probably genetically induced. In dominant trees the most efficient retranslocation of N was recorded in the upper crown and probably resulted from higher leaf temperatures and a longer senescent period in the sun leaves than in the shade leaves. Phosphorus retranslocation efficiency was higher in suppressed trees than in dominant ones, but no such tendency was observed with N. The most obvious difference between leaves at different crown levels concerned the time at which P translocation began; an outflow of P from leaves in the lower crown began in June, while in the upper crown this outflow did not begin until September/October.  相似文献   

20.
Early season leaf growth depends largely on nitrogen (N) provided by remobilization from storage, and many studies have tested the effect of N availability to roots on the amount of N provided for new leaf development by remobilization. Although it is well known that the light regime experienced by a leaf influences the amount of N per unit leaf area (LA), the effect of the local light regime on the amount of N derived either directly from root uptake or from remobilization for early season leaf growth has never been tested at an intra- canopy scale. The objective of this study was to quantify the relative importance of (1) N availability to roots, (2) local light regime experienced by the foliage (at the shoot scale) and (3) leaf rank along the shoot, on the total amount of N allocated to leaves and on the proportions of N provided by remobilization and root uptake. To quantify the importance of N uptake and remobilization as sources of leaf N, potted hybrid walnut trees (Juglans nigra L. x regia L.) were grown outdoors in sand and fed with a labeled ((15)N) nutrient solution. By removing the apical bud, the trees were manipulated to produce only two shoots. The experimental design had two factors: (1) high (HN; 8 mol N m(-3)) and low (LN; 2 mol N m(-3)) N availability; and (2) high (HL; 90% of incident photosynthetically active photon flux (PPF)) and low (LL; 10% of incident PPF) light. Total leaf N per tree was unaffected by either N availability or irradiance. The HN treatment increased the amount of leaf N derived from root uptake at the whole-tree scale (typically around 8 and 2% in the HN and LN treatments, respectively). Nitrogen allocation within foliage of individual trees was controlled by the local light regime, which strongly affected individual leaf characteristics as leaf mass per unit LA and area- based amount of leaf (N(a)). Decreasing the light availability to a branch decreased the amount of N allocated to it, benefiting the less shaded branches. In contrast, shading of the lower branch did not affect the fraction of total leaf N remobilized for either the lower, shaded branch or the upper, unshaded branch. The relevance of these findings for tree growth modeling is discussed.  相似文献   

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