A Dynamic Growth Model of Vegetative Soya Bean Plants: Model Structure and Behaviour under Varying Root Temperature and Nitrogen Concentration

A differential equation model of vegetative growth of the soyabean plant (Glycine max (L.) Merrill cv. ‘Ransom’)was developed to account for plant growth in a phytotron systemunder variation of root temperature and nitrogen concentrationin nutrient solution. The model was tested by comparing modeloutputs with data from four different experiments. Model predictionsagreed fairly well with measured plant performance over a widerange of root temperatures and over a range of nitrogen concentrationsin nutrient solution between 0.5 and 10.0 mmol in the phytotron environment. Sensitivity analyses revealedthat the model was most sensitive to changes in parameters relatingto carbohydrate concentration in the plant and nitrogen uptakerate. Key words: Glycine max (L.) Merrill, dry matter, nitrogen uptake, partitioning, photosynthesis, respiration, sensitivity analysis     

Relationships between root morphology and nitrogen availability in a recent theoretical model describing nitrogen uptake from soil

Abstract. The effect upon potential maximum nitrogen uptake rate of root morphology and nitrogen availability in soil was investigated using a simple nutrient transport model. Parameter values appropriate to an ecological or an agricultural context were introduced from the literature. The model predicted that the maximum uptake rate of nitrate was morphology-dependent only at extremely low concentrations. For ammonium, this was so for all realistic concentrations, assuming a high potential maximum uptake rate. The important concentration range for ammonium was two orders of magnitude greater than that for nitrate. With a lower potential maximum uptake rate of ammonium, root morphology was important below 15/igNg' soil, the concentration range in this case being a single order of magnitude greater than that for nitrate. The effects of root hairs were to decrease the threshold concentration for morphology-dependence, and to minimize root dry weight per unit volume of soil needed to maintain maximum nitrogen uptake rate. The effects of simultaneous mass flow of solution were negligible. The possible significance of these effects upon plant growth are discussed in relation to nitrogen availability.     

Dynamic model of the response of a vegetative grass crop to light, temperature and nitrogen

Abstract A previously described growth model of the vegetative grass crop is extended to include a simple representation of the root system, uptake of nitrogen from a soil nitrogen pool, and response to fertilizer application. The model simulates the processes of light interception, photosynthesis, partitioning of new growth, leaf area expansion, growth and maintenance respiration, ageing of plant tissues, senescence, recycling of substrates from senescing tissues, nitrogen uptake by the plant, leaching, mineralization, and fertilizer application. A principal component of the model, nitrogen uptake, is assumed to depend positively on plant carbon substrate concentration and soil nitrogen concentration, and to be inhibited by plant nitrogen substrate concentration. The dynamic responses to different levels of soil nitrogen, of shoot and root growth, nitrogen uptake and root activity, carbon and nitrogen plant substrate concentrations, and the fraction of substrate carbon used by the shoots, are examined; realistic behaviour is observed. The model predicts nitrogen fertilizer responses of yield and plant nitrogen content, which are compared directly with experimental data; good agreement is obtained.     

Modelling of the responses to nitrogen availability of two Plantago species grown at a range of exponential nutrient addition rates

Abstract. Plantago major ssp. major and P. lanceolata were grown in solution culture with exponential nutrient addition rates. Compared with P. lanceolata, P. major major showed a higher shoot weight ratio (SWR, fraction of plant dry weight in the shoot) and a higher net assimilation rate (NAR, expressed on a leaf dry weight basis) at equal plant (PNC) and shoot (SNC) nitrogen concentration, respectively. No difference was observed in shoot nitrogen ratio (SNR, fraction of plant nitrogen in the shoot) against PNC between the two species. The effect of these differences in matter partitioning and NAR on plant growth was examined by using a growth model. The model assumed (1) that the SWR and SNR are a linear function of PNC and (2) that the NAR is a rectangular hyperbolic function of SNC. Curvilinear relationships were observed between relative growth rate (RGR) and PNC. P. major major had a higher RGR at equal PNC and, thus, a higher nitrogen productivity (NP) than P. lanceolata. Steady-stale exponential growth was simulated for different nitrogen availability in the environment. P. major major had a higher RGR over the whole range of nitrogen availability but the difference attenuated with decreasing availability of nitrogen. The simulation also showed P. lanccolata having higher plasticity in the shoot/root ratio, which resulted from its higher variability in PNC.     

Nitrogen Uptake and Plant Growth II. An Empirical Model of Vegetative Growth and Partitioning

An empirical model of vegetative plant growth is presented.The model is based on experimental data on Polygonum cuspidatum,which showed (1) that the partitioning of dry matter and nitrogenamong organs was linearly related to the nitrogen concentrationof the whole plant and (2) that leaf thickness was negativelycorrelated with leaf nitrogen concentration. The model properlydescribes the behaviour of plants. Steady-state solutions ofthe model give the relative growth rate, specific leaf weight,and partitioning of dry matter and nitrogen among organs withthe net assimilation rate and the specific absorption rate asenvironmental variables. The effect of nitrogen removal on drymatter and nitrogen partitioning was examined as non-steady-statedynamic solutions of the model. The model predicted not onlyreduced leaf growth and enhanced root growth but also a fluxof nitrogen from the leaf to the root, which agreed with theexperimental results. Mathematical model, partitioning of dry matter and nitrogen, plant nitrogen, relative growth rate, shoot: root ratio, specific leaf weight     

Analysis of competition effects in mono- and mixed cultures of juvenile beech and spruce by means of the plant growth simulation model PLATHO

Inter- and intra-specific competition between plants for external resources is a critical process for plant growth in natural and managed ecosystems. We present a new approach to simulate competition for the resources light, water, and nitrogen between individual plants within a canopy. This approach was incorporated in a process-oriented plant growth simulation model. The concept of modelling competition is based on competition coefficients calculated from the overlap of occupied crown and soil volumes of each plant individual with the occupied volumes of its four nearest neighbours. The model was parameterised with data from a two-year phytotron experiment with juvenile beech and spruce trees growing in mono- and mixed cultures. For testing the model, an independent data set from this experiment and data from a second phytotron experiment with mixed cultures were used. The model was applied to analyse the consequences of start conditions and plant density on plant-plant competition. In both experiments, spruce dominated beech in mixed cultures. Based on model simulations, we postulate a large influence of start conditions and stand density on the outcome of the competition between the species. When both species have similar heights at the time of canopy closure, the model suggests a greater morphological plasticity of beech compared with spruce to be the crucial mechanism for competitiveness in mixed canopies. Similar to the experiment, in the model greater plasticity was a disadvantage for beech leading to it being outcompeted by the more persistent spruce.     

A simple model for nitrogen-limited plant growth and nitrogen allocation

BACKGROUND: and Aims In many studies of nitrogen-limited plant growth a linear relationship has been found between relative growth rate and plant nitrogen concentration, showing a negative intercept at a plant nitrogen concentration of zero. This relationship forms the basis of the nitrogen productivity theory. On the basis of empirical findings, several authors have suggested that there is also a distinctive relationship between allocation and plant nitrogen concentration. The primary aim of this paper is to develop a simple plant growth model that quantifies this relationship in mathematical terms. The model was focused on nitrogen allocation to avoid the complexity of differences in nitrogen concentrations in the different plant compartments. The secondary aim is to use the model for examining the processes that underlie the empirically based nitrogen productivity theory. METHODS: In the construction of the model we focused on the formation and degradation of biologically active nitrogen in enzymes involved in the photosynthetic process (photosynthetic nitrogen). It was assumed that, in nitrogen-limiting conditions, the formation of photosynthetic nitrogen is proportional to nitrogen uptake. Furthermore it was assumed that the degradation of photosynthetic nitrogen is governed by first-order kinetics. Model predictions of nitrogen allocation were compared with data from literature describing four studies of growth. Model predictions of whole plant growth were compared with the above-mentioned nitrogen productivity theory. KEY RESULTS: Allocation predictions agreed well with the investigated empirical data. The ratio of leaf nitrogen and plant nitrogen declines linearly with the inverse of plant nitrogen concentration. Nitrogen productivity is proportional to this ratio. Predictions for whole-plant growth were in accordance with the nitrogen productivity theory. CONCLUSIONS: The agreement between model predictions and empirical findings suggests that the derived equation for nitrogen allocation and its relationship to plant nitrogen concentration might be generally applicable. The negative intercept in the linear relationship between relative growth rate and plant nitrogen concentration is interpreted as being equal to the degradation constant of photosynthetic nitrogen.     

The influence of nitrogen availability on carbon and nitrogen storage in the biennial Cirsium vulgare (Savi) Ten. I. Storage capacity in relation to resource acquisition, allocation and recycling

Plants of Cirsium vulgare (Savi) Ten. were cultivated under five different nitrogen regimes in order to investigate the effects of nitrogen supply on the storage processes in a biennial species during its first year of growth. External N supply increased total biomass production without changing the relationship between ‘productive plant compartments’ (i.e. shoot plus fine roots) and ‘storage plant compartments’ (i.e. structural root dry weight, which is defined as the difference between tap root biomass and the amount of stored carbohydrates and N compounds). The amount of carbohydrates and N compounds stored per unit of structural tap root dry weight was not affected by external N availability during the season, because high rates of N supply increased the concentration of N compounds whilst decreasing the carbohydrate concentration, and low rates of N supply had the opposite effect. Mobilization of N from senescing leaves was not related to the N status of the plants. The relationship between nitrogen compounds stored in the tap root and the maximum amount of nitrogen in leaves was an increasing function with increasing nitrogen supply. We conclude that the allocation between vegetative plant growth and the growth of storage structures over a wide range of N availability seems to follow predictions from optimum allocation theory, whereas N storage responds in a rather plastic way to N availability.     

Physiological and growth responses of Centaurea maculosa (Asteraceae) to root herbivory under varying levels of interspecific plant competition and soil nitrogen availability

Summary Centaurea maculosa seedlings were grown in pots to study the effects of root herbivory by Agapeta zoegana L. (Lep.: Cochylidae) and Cyphocleonus achates Fahr. (Col.: Curculionidae), grass competition and nitrogen shortage (each present or absent), using a full factorial design. The aims of the study were to analyse the impact of root herbivory on plant growth, resource allocation and physiological processes, and to test if these plant responses to herbivory were influenced by plant competition and nitrogen availability. The two root herbivores differed markedly in their impact on plant growth. While feeding by the moth A. zoegana in the root cortex had no effect on shoot and root mass, feeding by the weevil C. achates in the central vascular tissue greatly reduced shoot mass, but not root mass, leading to a reduced shoot/root ratio. The absence of significant effects of the two herbivores on root biomass, despite considerable consumption, indicates that compensatory root growth occurred. Competition with grass affected plant growth more than herbivory and nutrient status, resulting in reduced shoot and root growth, and number of leaves. Nitrogen shortage did not affect plant growth directly but greatly influenced the compensatory capacity of Centaurea maculosa to root herbivory. Under high nitrogen conditions, shoot biomass of plants infested by the weevil was reduced by 30% compared with uninfested plants. However, under poor nitrogen conditions a 63% reduction was observed compared with corresponding controls. Root herbivory was the most important stress factor affecting plant physiology. Besides a relative increase in biomass allocation to the roots, infested plants also showed a significant increase in nitrogen concentration in the roots and a concomitant reduction in leaf nitrogen concentration, reflecting a redirection of the nitrogen to the stronger sink. The level of fructans was greatly reduced in the roots after herbivore feeding. This is thought to be a consequence of their mobilisation to support compensatory root growth. A preliminary model linking the effects of these root herbivores to the physiological processes of C. maculosa is presented.     

Equations relating growth and uptake of nitrogen by Salvinia molesta to temperature and the availability of nitrogen

Equations for predicting rates of growth, nitrogen content and rates of nitrogen uptake in Salvinia molesta Mitchell were derived from the literature and from new experiments. Equations for the effects of temperature specified zero growth below 5°C and above 43°C, with an optimum at 30°C and are applicable over a wider range than an Arrhenius model. They explained 74 and 55% of the variance in growth in numbers of leaves and weight, respectively, in a sewage lagoon where nutrients should not have been limiting. Equations for the effects of nitrogen content of the plant specified a four-fold, asymptotic increase in growth between 0.8% N and maximum growth above 5.0% N. Predictions from nitrogen contents explained 41% of the variance in growth in numbers of leaves in Papua New Guinea where temperatures fluctuated little. Top: root ratios rose from near 1.5 at 1% N to near 6.0 at 5% N. Rates of nitrogen uptake followed trends similar to rates of growth and nitrogen fixation supported a low rate of growth in the absence of nitrogen in solution.     

Nitrogen use efficiency by a slow-growing species as affected by CO2 levels, root temperature, N source and availability

This study examines the importance of N source and concentration on plant response to distinct CO₂ concentrations and root temperatures. The experimental design of this work was a factorial combination of: CO₂ concentration, nitrogen concentration, nitrogen source and root temperature. Carob (Ceratonia siliqua L.) was assessed as a potential model of a slow growing Mediterranean species.

The results showed that: 1) biomass increment under high CO₂ varied between 13 and 100 percnt; in relation to plants grown under the same conditions but at ambient CO₂ concentrations, depending on the root temperature and nitrogen source; 2) nitrate-fed plants attained a larger increase in biomass production compared to ammonium-fed ones. This performance seems to be linked to the co-ordinated regulation of the activities of glutamine synthetase and sucrose phosphate synthase. The variations in the magnitude and nature of growth responses to elevated CO₂ observed resulted in substantial changes in the chemical composition of the plant material and consequently in plant nitrogen use efficiency.

Although performed with seedlings and under controlled conditions, this work emphasizes the importance of the nitrogen source used by the plants, a factor rarely taken into consideration when forecasting plant responses to global changes. Particularly, the results presented here, highlight the potential for uncoupling biomass accumulation from increment of air CO₂ concentration and show that more than nitrogen availability N source may offset positive plant growth responses under elevated CO₂ and root temperature.     

Carbon allocation to shoots and roots in relation to nitrogen supply is mediated by cytokinins and sucrose: Opinion

In this paper we firstly show some general responses of biomass partitioning upon nitrogen deprivation. Secondly, these responses are explained in terms of allocation of carbon and nitrogen, photosynthesis and respiration, using a simulation model. Thirdly, we present a hypothesis for the regulation of biomass partitioning to shoots and roots.Shortly after nitrogen deprivation, the relative growth rate (RGR) of the roots generally increases and thereafter decreases, whereas that of the shoot decreases immediately. The increased RGR of the root and decreased RGR of the shoot shortly after a reduction in the nitrogen supply, cause the root weight ratio (root weight per unit plant weight) to increase rapidly.We showed previously that allocation of carbon and nitrogen to shoots and roots can satisfactorily be described as a function of the internal organic plant nitrogen concentration. Using these functions in a simulation model, we analyzed why the relative growth rate of the roots increases shortly after a reduction in nitrogen supply. The model predicts that upon nitrogen deprivation, the plant nitrogen concentration and the rate of photosynthesis per unit plant weight rapidly decrease, and the allocation of recently assimilated carbon and nitrogen to roots rapidly increases. Simulations show that the increased relative growth rate of the root upon nitrogen deprivation is explained by decreased use of carbon for root respiration, due to decreased carbon costs for nitrogen uptake. The stimulation of the relative growth rate of the root is further amplified by the increased allocation of carbon and nitrogen to roots. Using the simple relation between the plant nitrogen concentration and allocation, the model describes plant responses quite realistically.Based on information in the literature and on our own experiments we hypothesize that allocation of carbon is mediated by sucrose and cytokinins. We propose that nitrogen deprivation leads to a reduced cytokinin production, a decreased rate of cytokinin export from the roots to the shoot, and decreased cytokinin concentrations. A reduced cytokinin concentration in the shoot represses cell division in leaves, whereas a low cytokinin concentration in roots neutralizes the inhibitory effect of cytokinins on cell division. A reduced rate of cell division in the leaves leads to a reduced unloading of sucrose from the phloem into the expanding cells. Consequently, the sucrose concentration in the phloem nearby the expanding cells increases, leading to an increase in turgor pressure in the phloem nearby the leaf's division zone. In the roots, cell division continues and no accumulation of sugars occurs in dividing cells, leading to only marginal changes in osmotic potential and turgor pressure in the phloem nearby the root's cell division zone. These changes in turgor pressure in the phloem of roots and sink leaves affect the turgor pressure gradients between source leaf-sink leaf and source leaf-root in such a way that relatively more carbohydrates are exported to the roots. As a consequence RWR increases after nitrogen deprivation. This hypothesis also explains the strong relationship between allocation and the plant nitrogen status.     

A model for nutrient and water flow and their uptake by plants grown in a soilless culture

The objective of this study was to develop a sensitive means of control to optimize nutrient concentrations in the root zone of a soilless system, considering plant water and nutrient uptake, and solution circulation rates. A model is proposed to simulate ornamental plants growth in a channel with a non-interacting soilless substrate, irrigated by point sources with constant discharge rates, spaced uniformly along the channel. The model accounts for compensation for transpiration water losses and consequent salinity buildup, and its interactions with plant growth and nutrient uptake. The added water may contain given concentrations of nutrients and/or toxic (saline) compounds, which would cause salinity buildup. Uptake of each solute is specific, according to a Michaelis–Menten kinetics mechanism, but passive uptake by the transpiration stream is also accounted for. Plant growth is affected by time/age and ionic balance in the solution. The model was calibrated with lettuce (Lactuca sativa L.) plants grown in volcanic ash. Simulation of potassium concentration change as a result of discharge rate and emitter spacing revealed that the two parameters could compensate one for the other, once a target lower limit is set. Potassium appeared to be most sensitive to sodium accumulation in the growth medium; this accumulation changed ionic concentration balance, which affected pH and bicarbonate concentration. Passive uptake of calcium by the transpiration stream is highly affected by the root fraction involved, but its calculated contribution is below published values is highly affected by the root fraction involved, but its calculated contribution is below published values.     

Growth and maintenance respiration of roots of clonal Eucalyptus cuttings: scaling to stand-level

Root respiration consumes an important part of the daily assimilated carbon but the magnitude of this component of forest net ecosystem exchange and its partitioning among the different energy demanding processes in roots are still poorly documented. 5-month old Eucalyptus cuttings were grown in a greenhouse in pot filled with coarse sand. They were fertilized with three different amounts of a slow-release fertilizer with the doses of 8, 24 and 48 g of nitrogen per plant. Root respiration was measured using an infrared gas analyser by perfusing air through the pot on 9 plants per treatment on three dates 14 days apart. Measure of root respiration of the three treatments over time was made in order to obtain a large range of growth and nutrient uptake. Root respiration normalized at 22°C ranged from 0.09 to 0.23 g_C d^?1 for the three treatments during all the experiment. It was well predicted with a model that includes root growth rate and root nitrogen content.The nitrogen related maintenance coefficient was negatively correlated to the root nitrogen concentration suggesting a decrease in protein turnover with increasing fertility. Growth rate of fine root in a virtual stand was simulated using age-related allometric equations and further used to estimate root respiration in the field. Simulated root respiration increased over time from 0.39 to 3.14 g_C m^?2 d^?1 between 6 and 126 months assuming a turnover of 2 yr^?1 for fine roots. The major fraction of simulated root respiration in the field (78–92%) was used for the maintenance of the existing biomass.     

A model relating the maximum nitrate inflow of lettuce (Lactuca satvia L.) to the growth of roots and shoots

The net inflow of nitrate can be calculated from the nitrate concentration at the root surface by means of the Michaelis-Menten equation. Because of maximum inflow (Imax) is not constant but varies with plant age and growing conditions, a model for calculating Imax during plant growth was derived. Lettuce was grown in nutrient solution. Variations in temperature, radiation and plant age were used to vary growth rates and N-demand of plants. There was a linear relationship between relative growth rates (RGR) and maximum nitrate inflow (Imax), that could be described by the following regression function: Imax = 0.24 + 6.57 RGR. A residual analysis showed a further influence on Imax from the root:shoot-ratio (RSR), the effects of which could be accounted for by including an e-function in the relationship: Imax = (0.27 + 10.63 RGR) e^{(–0.0017 RSR)}. This model for calculating Imax was validated in two further experiments.     

Nutrient uptake and allocation at steady-state nutrition

Ingestad, T. and Ågren, G. I. 1988. Nutrient uptake and allocation at steady-state nutrition. - Physiol. Plant. 72: 450–459. Net nutrient uptake and translocation rates are discussed for conditions of steady-state nutrition and growth. Under these conditions, the relative uptake rate is equal to the relative growth rate, for whole plants as well as for plant parts, since the root/shoot ratio and internal concentrations remain stable. The nutrient productivity and the minimum internal concentration are parameters characteristic for the plant and the nutrient. A conceptual, mathematical model, based on these two fundamental parameters is used for calculation and prediction of the net nutrient uptake rate, which is required to maintain steady-state nutrition at a specified internal nutrient concentration or relative growth rate. When uptake rate is expressed on the basis of the root growth rate, there is, up to optimum, a strong linear relationship between uptake rate and the internal concentration of the limiting nutrient. More complicated and less consistent relationships are obtained when uptake rate is related to root biomass. The limiting factor for suboptimum uptake is the amount of nutrients becoming available at the root surface. When replenishment is efficient, e.g. with vigorous stirring, the concentration requirement at the root surface appears to be extremely low, even at optimum. In the suboptimum range of nutrition, the effect of nutrient status on root growth rate is a critical factor with a strong feed-back on nutrition, growth and allocation. At supraoptimum conditions, the uptake mechanism is interpreted as a protection against too high uptake rates and internal concentrations at high external concentration. In birch (Betula pendula Roth.), the allocation of nitrogen to the shoots is high compared to that of potassium and also to that of phosphorus at low nitrogen or phosphorus status. With decreasing stress, phosphorus allocation becomes more and more similar to nitrogen allocation. The formulation of a mathematical model for calculation of allocation of biomass and nutrients requires more exact information on the quantitative dependence of the growth-regulating processes on nutrition.     

The model symbiotic association between Medicago truncatula cv. Jemalong and Rhizobium meliloti strain 2011 leads to N-stressed plants when symbiotic N2 fixation is the main N source for plant growth

A better knowledge of the nitrogen nutrition of Medicago truncatula at the whole plant level and its modulation by environmental factors is a crucial step to reach a complete understanding of legume nitrogen nutrition. This study was based on the symbiotic system that is the most commonly used by the research community (M. truncatula cv. Jemalong A17 x Rhizobium meliloti strain 2011). Plant nitrogen nutrition was analysed in relation to carbon nutrition, under a range of nitrate concentrations in the nutrient solution and different light conditions. This study shows that this 'model symbiotic association' does not allow the plant to meet its nitrogen requirements, when dinitrogen fixation is the main nitrogen source for plant growth. A strong interaction between nitrogen and carbon nutrition was shown: when plant nitrogen requirements were not sustained, plant leaf area was much affected whereas photosynthesis per unit leaf area remained relatively stable. Both total nitrogen uptake and leaf area increased with increasing nitrate concentration in the nutrient solution; the magnitude of these responses varied according to the light conditions. Interestingly, the plant nitrogen nutrition level remained nearly unaffected by the light conditions. The observed nitrogen-limitation in this 'model symbiotic association' is an important finding for the research community. Based on practical recommendations regarding both the experimental conditions and the phenotypic traits to consider, a methodological framework was proposed to (i) help genomicists to assess plant nitrogen nutrition better, and (ii) assist in the detection of new genetic variants affected for nitrogen uptake in large-scale phenotyping studies.     

A dynamical model of environmental effects on allocation to carbon-based secondary compounds in juvenile trees

BACKGROUND AND AIMS: Patterns and variations in concentration of carbon-based secondary compounds in plant tissues have been explained by means of different complementary and, in some cases, contradictory plant defence hypotheses for more than 20 years. These hypotheses are conceptual models which consider environmental impacts on plant internal demands. In the present study, a mathematical model is presented, which converts and integrates the concepts of the 'Growth-Differentiation Balance' hypothesis and the 'Protein Competition' model into a dynamic plant growth model, that was tested with concentration data of polyphenols in leaves of juvenile apple, beech and spruce trees. The modelling approach is part of the plant growth model PLATHO that considers simultaneously different environmental impacts on the most important physiological processes of plants. METHODS: The modelling approach for plant internal resource allocation is based on a priority scheme assuming that growth processes have priority over allocation to secondary compounds and that growth-related metabolism is more strongly affected by nitrogen deficiency than defence-related secondary metabolism. KEY RESULTS: It is shown that the model can reproduce the effect of nitrogen fertilization on allocation patterns in apple trees and the effects of elevated CO(2) and competition in juvenile beech and spruce trees. The analysis of model behaviour reveals that large fluctuations in plant internal availability of carbon and nitrogen are possible within a single vegetation period. Furthermore, the model displays a non-linear allocation behaviour to carbon-based secondary compounds. CONCLUSIONS: The simulation results corroborate the underlying assumptions of the presented modelling approach for resource partitioning between growth-related primary metabolism and defence-related secondary metabolism. Thus, the dynamical modelling approach, which considers variable source and sink strengths of plant internal resources within different phenological growth stages, presents a successful translation of existing concepts into a dynamic mathematical model.     

硝态氮（NO3^—）对水稻侧根生长及其氮吸收的影响

侧根是植物吸收利用土壤养分的重要器官 ,其生长发育受内部遗传因子和外部环境矿质养分的影响。通过琼脂分层培养发现 :局部供应NO-3 可以诱导水稻 (OryzasativaL .)主根或不定根上侧根的生长。为研究旱种条件下NO-3 对水稻侧根发育及其N吸收的影响 ,设置了 3个蛭石培养实验 :分根处理、全株缺N、全株供N处理。分根处理 (一半根系供应 3mmol/LKNO3,另一半根系供应 3mmol/LKCl)结果表明 :局部供应NO-3 能够促进水稻侧根生长。而在全株处理下 ,N饥饿诱导了侧根的伸长。水稻根系对NO-3 的这两种反应都存在着显著的基因型差异。同时对地上部N浓度、可溶性总糖含量及N含量分析表明 ,这些生理指标在分根处理与全株加N处理中的差异均不显著 ,表明分根处理也能基本满足植株正常生长对N的需求。在分根处理中 ,水稻的N含量与分根处理中供N一侧的平均侧根长度存在显著正相关 ,这表明在养分不均一的介质中 ,侧根长度对水稻N素吸收具有十分重要的作用。而在N素充足的条件下 ,两者之间的相关性并不显著 ,这暗示在养分充足的环境下 ,侧根长度可能并不是决定根系吸收N素的主要因素     

局部根区水分胁迫下氮形态与供给部位对玉米幼苗生长的影响

通过向玉米幼苗分根装置一侧根室的营养液中加入聚乙二醇(PEG 6000)来模拟植物水分胁迫,并设3种供氮形态(硝态氮、铵态氮、两者各占50%的混合氮),且只加入到一侧根室(当氮加入到和PEG同侧时为水氮异区,加入到无PEG一侧时为水氮同区),测定各处理的光合、生理指标,以研究局部根区水分胁迫下氮形态与供给部位对玉米幼苗生长的影响.结果表明:同一氮形态供给下水氮同区植株的光合速率(Pn)、最大净光合速率(Pmax)、光饱和点(LSP)、CO2饱和点(CSP)、叶绿素a、b及叶绿素总含量、根系活力、氮含量和生物量高于水氮异区,光呼吸速率(Rp)、CO2补偿点(CCP)、木质部汁液脱落酸(ABA)浓度、氮利用效率、水分利用效率低于水氮异区;供混合氮和硝态氮的植株Pn、Pmax、LSP、CSP、氮含量和生物量高于供铵态氮的植株,而CCP、Rp、木质部汁液ABA浓度、氮利用效率、水分利用效率变化趋势则相反.可见,同一供氮形态下,水氮同区比水氮异区更利于植物生长,而水氮利用效率在水氮异区下较高;混合氮和硝态氮对植物生长的促进作用优于单一供给铵态氮,但铵态氮更有利于提高水氮利用效率.