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1.
Carbon distribution in the stem of 2-year-old cork oak plants was studied by (14)CO(2) pulse labeling in late spring in order to trace the allocation of photoassimilates to tissue and biochemical stem components of cork oak. The fate of (14)C photoassimilated carbon was followed during two periods: the first 72 h (short-term study) and the first 52 weeks (long-term study) after the (14)CO(2) photosynthetic assimilation. The results showed that (14)C allocation to stem tissues was dependent on the time passed since photoassimilation and on the season of the year. In the first 3 h all (14)C was found in the polar extractives. After 3 h, it started to be allocated to other stem fractions. In 1 day, (14)C was allocated mostly to vascular cambium and, to a lesser extent, to primary phloem; no presence of (14)C was recorded for the periderm. However, translocation of (14)C to phellem was observed from 1 week after (14)CO(2) pulse labeling. The phellogen was not completely active in its entire circumference at labeling, unlike the vascular cambium; this was the tissue that accumulated most photoassimilated (14)C at the earliest sampling. The fraction of leaf-assimilated (14)C that was used by the stem peaked at 57% 1 week after (14)CO(2) plant exposure. The time lag between C photoassimilation and suberin accumulation was ～8 h, but the most active period for suberin accumulation was between 3 and 7 days. Suberin, which represented only 1.77% of the stem weight, acted as a highly effective sink for the carbon photoassimilated in late spring since suberin specific radioactivity was much higher than for any other stem component as early as only 1 week after (14)C plant labeling. This trend was maintained throughout the whole experiment. The examination of microautoradiographs taken over 1 year provided a new method for quantifying xylem growth. Using this approach it was found that there was more secondary xylem growth in late spring than in other times of the year, because the calculated average cell division time was much shorter. 相似文献
2.
海岸带沙荒风口木麻黄无性系造林效果的综合评价 总被引：2，自引：1，他引：2
以木麻黄无性系的防护效能和速生丰产性能为基础,运用多目标决策方法,对沿海沙荒风口6种木麻黄无性系造林效果进行综合评价,结果表明:在沙荒风口造林的6种木麻黄无性系中,粤501最抗风,其防护效能最高,平18次之;平18最速生丰产,粤501其次;莆20在6种无性系中无论抗风性还是速生丰产性能均最低。综合评价指标以平18最高,粤501次之,莆20最小。平18和粤501是沿海沙荒风口造林理想的木麻黄无性系。 相似文献
3.
We studied the distribution and retranslocation of N in 11-year-old Pinus contorta Dougl. trees following a winter application of N at 100 kg ha(-1) as (15)N-urea, (15)NH(4)NO(3) or NH(4) (15)NO(3). In all treatments, there was little uptake of (15)N after the first growing season although labeled N was still present in the soil. In subsequent years, (15)N in the trees was partly retranslocated, and, at the same time, it was diluted by uptake of unlabeled N from the soil. Between Years 1 and 8 after N fertilization, net retranslocation of (15)N from the lower crown (branches formed before fertilization) was 14%, and 18-25% of the (15)N in the trees was translocated to the upper and mid-crown. Overall, uptake of (15)N from nitrate was less than from urea or ammonium. However, when compared with the urea- and ammonium-N sources, (15)N from the nitrate source initially moved as rapidly into the foliage, but a greater proportion of it was retranslocated from the foliage during the second growing season. Nitrogen in foliage and wood formed in the growing season following fertilization was more highly labeled (measured as % N derived from the fertilizer) than in recently formed tissues. Labeling was substantially higher in foliage formed before fertilization than in wood of a similar age. In contrast, N in foliage formed after fertilization had only slightly higher labeling than wood of a similar age, indicating a relatively stable labeling throughout the trees once (15)N uptake had ceased. The concentrations of total and labeled N were substantially higher in foliage than in either wood or bark. There was evidence of N movement into wood tissues formed before fertilization, presumably along rays, and also of N retranslocation out of xylem cells as they matured. This study of internal N cycles was facilitated by the use of (15)N labeling because there was little uptake of labeled N after the first growing season, whereas interpretation based on total N was obscured by substantial uptake of N from the soil. We conclude that retranslocation studies based on measurements of total N content should be avoided. 相似文献
4.
Nygren P 《Tree physiology》1995,15(2):71-83
An idealized model was developed to describe leaf CO(2) exchange in the leguminous tree Erythrina poeppigiana (Walpers) O.F. Cook under well-watered field conditions. Photosynthetic rate in mature leaves (p) was modeled as a rectangular hyperbolic function of photon flux density (q) and ambient CO(2) concentration (c(a)), relative photosynthetic capacity (pi) was modeled as a logistic s-function of leaf age (l(a)), metabolic dark respiration rate (r(m)) was modeled as an exponential function of leaf temperature (T(l)), and photorespiration rate (r(p)) was modeled as a hyperbolic function of c(a). Assimilation rate (a(c)) was modeled as the difference between the product of p and pi and the sum of r(m) and r(p): a(c) = p(q,c(a))pi(l(a)) - [r(m)(T(l)) + r(p)(c(a))]. The model parameters were estimated separately for five sources of E. poeppigiana (Clones 2660, 2662, 2687 and 2693 and half-sib Family 2431) from field data measured with a portable closed-loop gas exchange system at a humid tropical site in Costa Rica. The between-source differences in leaf CO(2) exchange characteristics were small, but statistically significant. Aboveground biomass production was highest in sources that maintained high relative photosynthetic capacity throughout the leaf life span. Quantum yield varied between 0.046 and 0.067, and light-saturated assimilation rate (q = 2000 micro mol m(-2) s(-1) and T(l) = 28 degrees C) at natural atmospheric c(a) (350 micro mol mol(-1)) was 16.8-19.9 micro mol m(-2) s(-1). Increasing c(a) to 1000 micro mol mol(-1) resulted in an approximate doubling of the light-saturated assimilation rate. Foliole nitrogen concentration, which was 45.3-51.2 mg g(-1) in mature leaves, was positively correlated with relative photosynthetic capacity. Foliole nitrogen concentration, quantum yield and maximum assimilation rate of E. poeppigiana are among the highest values observed in tropical woody legumes. 相似文献
5.
Göransson A 《Tree physiology》1999,19(2):111-116
Small birch plants (Betula pendula Roth) were cultivated in a hydroponic spray solution where the relative growth rate (R(G); day(-1)) was controlled by the relative supply rate of zinc (R(Zn); day(-1)). After an adjustment phase to steady-state growth, R(G) equaled R(Zn). The R(Zn) treatments were 0.05, 0.125 and 0.20 day(-1) with free access to all other nutrients. In an additional treatment, there was free access to all nutrients, including zinc (FA treatment). The pH of the nutrient solution was approximately 4.5 and conductivity was 100 &mgr;S cm(-1). The duration of each treatment depended on R(Zn) and ranged from 4 (FA treatment) to 10 weeks (at R(Zn) = 0.05 day(-1)). The plants showed persistent and typical zinc-deficiency symptoms at steady-state growth when R(G) was 0.05 and 0.125 day(-1), whereas there were few symptoms when R(G) was 0.2 day(-1). The Zn concentration of the plants ranged from 8 (at R(Zn) = 0.05 day(-1)) to 21 &mgr;g g(DM) (-1) (DM = dry mass) (at R(Zn) = 0.2 day(-1)) and was approximately 42 &mgr;g g(DM) (-1) in the FA treatment. Uptake rates of Zn, calculated per root growth rate (&mgr;mol g(DM, root) (-1)), were about 2.8 times higher at R(Zn) = 0.20 day(-1) than at R(Zn)= 0.05 day(-1). The root and stem biomass fractions were approximately constant at all supply rates of Zn, whereas the leaf biomass fraction tended to increase with increasing supply rate of Zn. Net assimilation rate was constant from FA to an R(Zn) of 0.125 day(-1) but decreased by a factor of about 2 at R(Zn) = 0.05 day(-1). Leaf area ratio and specific leaf area were smaller at low supply rates of zinc than at high supply rates. 相似文献
6.
测定了不同土壤水分条件下黄栌光合作用的CO2响应过程,采用直角双曲线修正模型对其响应过程进行拟合。结果表明:黄栌的净光合速率(Pn)对土壤水分的变化具有显著的阈值响应。维持黄栌较高光合速率的RWC在42.1%-73.6%(MWC在11.0%-19.2%)之间时,最适宜的RWC为61.7%(MWC为16.1%)左右。黄栌的羧化效率(CE)、光合能力(Pnmax)、光呼吸速率(Rp)表现为对土壤水分具有明显的阈值响应,当RWC为61.7%(MWC为16.1%)时CE、Pnmax达到最大值,当RWC为73.6%(MWC为19.2%)时Rp达到最大值。黄栌的CO2补偿点(Γ)、CO2饱和点CSP随着土壤含水量的增加表现出先下降后上升的规律。 相似文献
7.
Uptake and efflux of (36)Cl(-), (45)Ca(2+) and (42)K(+) were measured in water-infiltrated detached needles from Sitka spruce (Picea sitchensis (Bong.) Carr.) trees incubated in 1 mol m(-3) KCl or CaCl(2) or 2 mol m(-3) NaCl solutions or in artificial rain water containing mmol m(-3) amounts of these ions. Surface efflux was measured separately from leakage from the cut ends of the needles. Needles loaded with (36)Cl(-) and killed in liquid N(2) before elution displayed a rapid and extensive loss of radioisotope, indicating that mesophyll cell membranes were the limiting factor for (36)Cl(-) exchange. Data for live needles revealed a novel phase of (36)Cl(-) efflux, with an exchange halftime of about 20 min, which was faster than that for either the vacuole or the cytoplasm, but much slower than that for the free space. The novel phase was interpreted as representing diffusion of Cl(-) through the predominantly negatively charged cuticle. Killing needles loaded with (45)Ca(2+) or (42)K(+) also increased efflux relative to that from live needles, but only to a limited degree, indicating that the main factor limiting cation efflux was the cuticle. During the first hours of (45)Ca(2+) uptake, the isotherms displayed a shoulder, indicating that there was a significant Donnan free space phase in the cuticle for Ca(2+). A shoulder was absent from (42)K(+) uptake isotherms because of the preferential adsorption of divalent cations on the exchange sites. 相似文献
8.
以马来海松酸(MPA)、新戊二醇(NPG)、三羟甲基丙烷(TMP)、间苯二甲酸(IPA)、己二酸(AA)、间苯二甲酸-5-磺酸钠(5-SSIPA)为原料,采用先分步熔融后溶剂回流法制得水可分散型松香基聚酯多元醇(WDRPP)。探讨了反应时间、催化剂用量、n(—OH)∶n(—COOH)和亲水单体用量对反应的影响,并利用傅里叶红外光谱(FT-IR)和~(13) C NMR对产物进行了表征。利用热重分析(TG)研究了WDRPP的耐热性,并采用Coats-Redfem法对WDRPP的热分解动力学试验数据进行拟合分析,得到动力学参数。结果表明,当反应时间为5.5 h(熔融反应3 h,溶剂回流2.5 h),催化剂用量为0.10%,n(—OH)∶n(—COOH)为1.4∶1,亲水单体用量为2.86%时,制备的WDRPP的热稳定性和WDRPP水分散体的稳定性最佳;WDRPP的最大失重速率温度(Tmax)为406.7℃、热解反应活化能为64.65 k J/mol,且热分解动力学曲线线性良好(R~2=0.997 3),表明WDRPP热分解过程符合一级反应动力学规律;FT-IR和~(13) C NMR的分析结果表明WDRPP制备成功。 相似文献
9.
从 Madhupur 林区的不同地点采集了 Acacia auriculi-formis A. Cunn. ex Benth., A. mangium Wild., Artocarpus het-erophyllus Lamk. C., Dalbergia sissoo Roxb. ex A. P. D., Euca-lyptus camaldulensis Dehnn., Hevea brasiliensis (Wild. ex Juss) Muell. Arg., Swietenia macrophylla King. and Tectona grandis L. 8个树种的根和根际土。采用简单常规的根围土壤真菌孢子分离、形态鉴定和树木细根染色、显微镜观察等方法,进行了孟加拉国Madhupur林区内不同森林树种中丛枝菌根多样性的研究。图2表2参46。 相似文献
10.
应用田间根系分区供水方法,研究根系分区交替水分胁迫(APRD)、固定单侧水分胁迫(FPRD)与对照两侧同时供水(BPRI)对2年生草乌光合特性的影响。结果表明:1)各水分条件下,叶片蒸腾速率(Tr)随着周期的进行逐渐减小,后期随着处理水分亏缺的加重,峰值减小,峰出现时间前移;2)APRD处理下,草乌通过维持相对较低的气孔导度(Gs),在Tr降低30%的前提下,Pn比对照BPRI与FPRD处理分别提高4.16%,37.43%,反映出APRD处理对气孔的优化调节;3)各水分条件下,草乌的水分利用效率(WUE)日变化均呈双峰曲线,APRD处理可显著提高草乌的WUE,分别比对照BPRI和FPRD处理提高20.39%和10.53%,对草乌在干旱地区栽培意义重大;4)各水分条件下草乌的光合-光响应曲线变化趋势基本一致,表观量子效率(AQY)差异不显著,光饱和点(LSP)和光补偿点(LCP)协同变化表明APRD处理在一定程度上增强了草乌对光环境的适应能力;最大净光合速率(Pmax)表现为APRD处理下最高,FPRD处理略低于对照BPRI;APRD处理下,草乌叶片暗呼吸速率(Rd)最低,有利于干物质积累。根系分区交替水分胁迫通过供水调控挖掘了草乌本身的生物学节水潜力。 相似文献
11.
用二次正交旋转组合设计优化马占相思增殖培养基 总被引：5，自引：0，他引：5
在马占相思组织培养初步取得成功的基础上，采用二次正交旋转组合设计对马占相思增殖培养基进行优化，建立增殖率(Y)对Ca^2 浓度(X1)、6-BA浓度(X2)及NAA浓度(X3)3个试验因子的正交回归模型：Y=2．280-0．168X1-0．259X2 0．185X1^2-0．210X2^2 0．167X3^2 0．326X1X2。从模型推知，当Ca^2 浓度为0．58倍常规MS培养基浓度(255g／L)，6BA为0．76mg／L，NAA为0．16mg／L时，增殖率达最大值为4．32，实验结果与预测值相符。 相似文献
12.
Van Den Driessche R 《Tree physiology》1991,8(3):289-295
New root growth of conifer nursery seedlings is dependent on light, but whether this is necessary only for photosynthesis, or also has some other root growth promoting effect is unknown. This question was investigated using one-year-old Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) seedlings grown at two nurseries from the same seed lot and taken from cold storage in March and April. New root production was examined in two 10-day root growth capacity (RGC) experiments. Seedlings were subjected to one of four treatments: (1) control, (2) exclusion of light, (3) low CO(2) concentration, and (4) girdling to separate the phloem connection between shoot and root. Shoots were enclosed in Plexiglas cuvettes and supplied with scrubbed air to reduce the CO(2) concentration to 11 to 22 microl l(-1) in the light. The closed system used in Experiment 1 was opened to the atmosphere briefly each day to restore O(2) to ambient, but this was unnecessary for the open system used in Experiment 2. In Experiment 1, new root production was affected by treatments in the order: control > low CO(2) concentration > dark > girdling. Greater new root production in the low CO(2) treatment compared with the dark treatment was attributed to brief increases in CO(2) to ambient concentrations when O(2) was restored each day. In Experiment 2, new root production at the low CO(2) concentration in the light was essentially the same as in darkness, but only 17% of the control value. Thus light appeared to play no part in new root production other than permitting photosynthesis. Limited production of new roots occurred in the absence of photosynthesis, which was further reduced by girdling, presumably because, after girdling, only root system reserves could be used. 相似文献
13.
Net efflux of CO(2) from attached avocado (Persea americana Mill.) fruit was measured periodically from three weeks after anthesis to fruit maturity. Net CO(2) exchange was determined in daylight (light respiration, R(l)) at a photosynthetic photon flux (PPF) greater than 600 micromol m(-1) s(-1), and in the dark (dark respiration, R(d)). Dark respiration and R(l) were highest during the early cell division stage of fruit growth (about 25 and 22 nmol CO(2) g(dw) (-1) s(-1), respectively) and decreased gradually until fruit maturity to about 1 and 0.5 nmol CO(2) nmol CO(2) g(dw) (-1) s(-1), respectively. Fruit photosynthesis, calculated from the difference between R(d) and R(l), ranged from 0.5 to 3.1 nmol CO(2) g(dw) (-1) s(-1). Net rate of CO(2) assimilation on a fruit dry weight basis was highest during the early stages of fruit growth and reached the lowest rate at fruit maturity. Net rate of CO(2) assimilation of fruit exposed to light was 0.4 to 2.5% of that for fully expanded leaves. Although the relative amount of carbon assimilated by the fruit was small compared with the total amount of carbon assimilated by the leaves, the data indicate that avocado fruit contribute to their own carbon requirement by means of CO(2) assimilated in the light. 相似文献
14.
Three controlled water supply treatments were applied to 1-year-old peach trees grown in root observation boxes. The treatments were: I(0), growth medium maintained at 50% field capacity; I(1), water supplied when daily net tree stem diameter change was negative or zero for 1 day; I(3) as for I(1) except that water was applied after net daily stem diameter change was negative or zero for 3 consecutive days. Trees in treatment I(0) had the greatest mean daily first-order shoot growth rates, and trees in treatment I(3) had the lowest shoot growth rates. Because leaf production rate (apparent plastochron) of first-order shoots was unaffected by treatment, differences in shoot length were due to differences in internode extension and not to the number of internodes. Trees in treatment I(0) had a greater number of second-order shoot axes than trees in treatment I(1) or I(3). Furthermore, an increase in the rate of growth of the first-order shoot axis was associated with an increased tendency for branching (i.e., the development of sylleptic second-order shoots). Increased leaf length was also associated with more frequent watering. Trees in treatment I(0) had the greatest root lengths and dry weights, and this was attributed to a greater number of first-and second-order (lateral) root axes compared with trees in the I(1) and I(3) treatments. The extension rate and apical diameter of first-order roots were reduced by the I(3) treatment. The density of second-order roots along primary root axes was not affected by any of the treatments. 相似文献
15.
以萜烯基环氧树脂(TME)与新戊二醇(NPG)反应,合成了萜烯基环氧树脂基多元醇(T-N),再以端羟丙基聚硅氧烷(HTP)、2,4-甲苯二异氰酸酯(TDI)及2,2-二(羟甲基)丙酸(DMPA)改性T-N,制备了阴离子型聚硅氧烷改性萜烯基环氧树脂多元醇(T-N-S)水分散体,并以红外光谱(FT-IR)、核磁共振光谱(NMR)表征了多元醇的化学结构。研究了反应条件、改性剂HTP用量等对多元醇水分散体稳定性及微观结构的影响。结果表明:DMPA与TDI物质的量比为1∶2,丙酮为溶剂(用量为反应物总质量的1.5~2倍),丙酮回流温度(56℃)下反应3 h,再加入T-N及HTP,继续反应4 h,所合成的T-N-S能够较好地在水中分散。透射电子显微镜分析表明,当HTP用量为T-N质量的3%~12%时,制备的T-N-S水分散体粒子均为球形粒子,粒径范围100~300 nm。 相似文献
16.
We used 20-mm-long, Granier-type sensors to quantify the effects of tree size, azimuth and radial position in the xylem on the spatial variability in xylem sap flux in 64-year-old trees of Taxodium distichum L. Rich. growing in a flooded forest. This information was used to scale flux to the stand level to investigate variations in half-hourly and daily (24-hour) sums of sap flow, transpiration per unit of leaf area, and stand transpiration in relation to vapor pressure deficit (D) and photosynthetically active radiation (Q(o)). Measurements of xylem sap flux density (J(s)) indicated that: (1) J(s) in small diameter trees was 0.70 of that in medium and large diameter trees, but the relationship between stem diameter as a continuous variable and J(s) was not significant; (2) J(s) at 20-40 mm depth in the xylem was 0.40 of that at 0-20 mm depth; and (3) J(s) on the north side of trees was 0.64 of that in directions 120 degrees from the north. Daily transpiration was linearly related to daily daytime mean D, and reached a modest value of 1.3 mm day(-1), reflecting the low leaf area index (LAI = 2.2) of the stand. Because there was no soil water limitation, half-hourly water uptake was nearly linearly related to D at D < 0.6 kPa during both night and day, increasing to saturation during daytime at higher values of D. The positive effect of Q(o) on J(s) was significant, but relatively minor. Thus, a second-order polynomial with D explained 94% of the variation in J(s) and transpiration. An approximately 40% reduction in LAI by a hurricane resulted in decreases of about 18% in J(s) and stand transpiration, indicating partial stomatal compensation. 相似文献
17.
小蓬草鲜叶正己烷提取物化学组分分析 总被引：1，自引：0，他引：1
利用气质联用仪（GC-MS）对小蓬草（Conyza canadensis）鲜叶正己烷提取物化学组分进行了分析,结果表明其化学组分中右旋-柠檬烯相对含量（50.09%）最高,其次是（顺,顺,顺）-9,12,15-十八碳三烯-1-醇（15.71%）,再次是顺-3,7-二甲基-1,3,6-辛三烯（罗勒烯）（11.21%）。小蓬草鲜叶正己烷提取物化学组分主要是萜烯类化合物（占69.89%）,右旋-柠檬烯是小蓬草鲜叶正己烷提取物化学组分的主要特征成分之一。柠檬烯是香料,又是具有化感潜力的物质,小蓬草可以作为开发植物精油或植物源除草剂的植物资源,具有综合开发利用价值。 相似文献
18.
Foliage, fine-root, woody-tissue and stand respiration in Pinus radiata in relation to nitrogen status 总被引：1，自引：0，他引：1
We measured respiration of 20-year-old Pinus radiata D. Don trees growing in control (C), irrigated (I), and irrigated + fertilized (IL) stands in the Biology of Forest Growth experimental plantation near Canberra, Australia. Respiration was measured on fully expanded foliage, live branches, boles, and fine and coarse roots to determine the relationship between CO(2) efflux, tissue temperature, and biomass or nitrogen (N) content of individual tissues. Efflux of CO(2) from foliage (dark respiration at night) and fine roots was linearly related to biomass and N content, but N was a better predictor of CO(2) efflux than biomass. Respiration (assumed to be maintenance) per unit N at 15 degrees C and a CO(2) concentration of 400 micro mol mol(-1) was 1.71 micro mol s(-1) mol(-1) N for foliage and 11.2 micro mol s(-1) mol(-1) N for fine roots. Efflux of CO(2) from stems, coarse roots and branches was linearly related to sapwood volume (stems) or total volume (branches + coarse roots) and growth, with rates for maintenance respiration at 15 degrees C ranging from 18 to 104 micro mol m(-3) s(-1). Among woody components, branches in the upper canopy and small diameter coarse roots had the highest respiration rates. Stem maintenance respiration per unit sapwood volume did not differ among treatments. Annual C flux was estimated by summing (1) dry matter production and respiration of aboveground components, (2) annual soil CO(2) efflux minus aboveground litterfall, and (3) the annual increment in coarse root biomass. Annual C flux was 24.4, 25.3 and 34.4 Mg ha(-1) year(-1) for the C, I and IL treatments, respectively. Total belowground C allocation, estimated as the sum of (2) and (3) above, was equal to the sum of root respiration and estimated root production in the IL treatment, whereas in the nutrient-limited C and I treatments, total belowground C allocation was greater than the sum of root respiration and estimated root production, suggesting higher fine root turnover or increased allocation to mycorrhizae and root exudation. Carbon use efficiency, the ratio of net primary production to assimilation, was similar among treatments for aboveground tissues (0.43-0.50). Therefore, the proportion of assimilation used for construction and maintenance respiration on an annual basis was also similar among treatments. 相似文献
19.
根据与核桃早实性状连锁的RAPD标记OPB-08958序列,设计SEA-F/SEA-R和SEB-F/SEB-R2对SCAR引物。在亲本、杂交后代和栽培品种(系)中的检测结果表明:SEA-F/SEA-R引物对在早实亲本‘绿园’中能稳定扩增出SCAR-SEA958特异标记;在‘绿园’ב绿丰’杂交F1后代群体中,SCAR-SEA958标记与核桃早实性状共分离,与核桃早实性状间的遗传距离为1.99cM;用晚实优系‘T-12’和栽培品种‘元丰’及‘T-12’ב元丰’杂交F1后代,检测SCAR-SEA958标记的分离情况,SCAR-SEA958与核桃早实性状共分离;在9个核桃栽培品种(系)中,SCAR-SEA958在8个供试品种的7个早实品种上出现,在1个早实品种‘鲁光’和1个晚实优系‘T-12’上没有扩增出条带。SCAR-SEA958标记在不同遗传背景下有较高的稳定性。 相似文献
20.
Growth of a single sugi (Cryptomeria japonica (L.f.) D. Don.) tree was analyzed on the basis of a dry matter budget. The aboveground net production rate and death rate were defined as the anabolic rate and catabolic rate, respectively. Growth rate of aboveground tree weight, v(w) (kg(dw) year(-1)), was defined as follows: v(w) = v(p) - v(d) (1) where v(p) (kg(dw) year(-1)) is the aboveground net production rate and v(d) (kg(dw) year(-1)) is the aboveground death rate. The value of v(d) is obtained by measuring the monthly clippings of new dead leaves and branches attached to a sample tree. The value of v(w) was calculated as the annual difference in the estimated aboveground tree weight, w(T) (kg(dw)). Finally, the value of v(p) was estimated as the sum of the values of v(d) and v(w). The following allometric relationships were found between v(p) and w(T) and between v(d) and w(T): v(p) = aw(T) (alpha), v(d) = bw(T) (beta) (2). Combining Equations 1 and 2 gives a growth equation, Bertalanffy's equation, of the sample tree. dw(T)/dt = v(w) = aw(T) (alpha) - bw(T) (beta) (3). Because the growth curve of w(T) was derived from Equation 3, the analysis of the growth of w(T) is based on direct measurement of the dry matter budget. 相似文献