Cyanide-Resistant Root Respiration and Tap Root Formation in Two Subspecies of Hypochaeris radicata

Root respiration of the tap root forming species Hypochaeris radicata L. was measured during tap root formation. A comparison was made of two subspecies: H. radicata L. ssp. radicata L., a subspecies from relatively rich soils, and H. radicata L. ssp. ericetorum Van Soest, a subspecies from poor acidic soils. Root respiration was high and to a large extent inhibited by hydroxamic acid (SHAM) before the start of the tap root formation, indicating a high activity of an alternative non-phosphorylative electron transport chain. The rate of root respiration was much lower and less sensitive to SHAM when a considerable tap root was present. However, root respiration was also cyanide-resistant when a tap root was present, indicating that the alternative pathway was still present. A decreased rate of root respiration coincided with an increase of the content of storage carbohydrates, mainly in the tap root. The level of reducing sugars was constant throughout the experimental period, and it was concluded that the activity of the alternative oxidative pathway was significant in oxidation of sugars that could not be utilized for purposes like energy production, the formation of intermediates for growth or for storage. Root respiration decreased after the formation of a tap root. This decrease could neither be attributed to a gradual disappearance of the alternative chain, nor to a decreased level of reducing sugars. No differences in respiratory metabolism between the two subspecies have been observed, suggesting that a high activity of the alternative oxidative pathway is not significant in adaptation of the present two subspecies to relatively nutrient-rich or poor soils.     

Storage of Osmotically Active Compounds in the Taproot of Daucus carota L.

The osmotic potential of cell sap from the storage root, lateralroots and shoots of carrot (Daucus carota L., cv. AmsterdamseBak) was calculated from the concentration of osmotically activecompounds in these tissues. The osmotic potential of the taprootdid not change with age prior to and during the storage of osmoticallyactive sugars, as sucrose and reducing sugars. The increased contribution of soluble sugars in the osmoticpotential was accompanied by a proportionally decreased contributionof potassium and organic acids. Before storage of soluble sugarsin the taproot occurred, potassium and organic acids contributed80% to the total osmotic value, in contrast with lateral roottissue, where potassium and nitrate were the main osmotic solutes.The concentration of osmotically active solutes was lower inlateral root tissue than in storage root tissue. Shoot tissueresembled taproot tissue before storage, in having potassiumand organic acids as the main osmotic solutes. The concentrationof osmotically active solutes was highest in shoot tissue andit increased towards the end of the experimental period. The calculated osmotic potentials were in good agreement withthe experimental values, as determined from the molecular depressionof the freezing point of cell sap. Storage of reducing sugarsand sucrose is discussed in relation to acid and neutral invertaseactivities. Key words: Daucus carota, Osmotic solutes, Sugar storage, Invertase activity     

The physiological significance of cyanide-resistant respiration in higher plants

Abstract A brief survey of the biochemistry of the alternative oxidative pathway (‘cyanide-resistant respiration’) and its occurrence in vivo is given. Several hypotheses about the physiological significance of the alternative chain are discussed. These include a role in (1) heat production, (2) fruit ripening, (3) respiration of plants that contain high levels of cyanogenic glycosides, producing HCN upon wounding, (4) oxidation of NADH that is produced by various causes in excess of that required for ATP production, (5) ion uptake, and (6) osmoregulation. In intact roots of higher plants, the activity of the alternative pathway is more active when less carbohydrate is required for assimilation of N (NH+₄ NO-₃ or N₂) and is less active in those when carbohydrates are being stored in a storage organ or when the availability of photosynthate is reduced. An increase in carbohydrate requirement for osmoregulation is also correlated with decreased alternative chain activity. It is concluded that the alternative pathway in roots plays an important role in oxidation of sugars which are not required for carbon skeletons, energy production for growth and maintenance processes, osmoregulation or storage. However, the significance of this role may vary in different tissues and physiological states.     

An architectural analysis of the elongation of field-grown sunflower root systems. Elements for modelling the effects of temperature and intercepted radiation

The effects of photosynthetic photon flux density (PPFD) andsoil temperature on root system elongation rate have been analysedby using an architectural framework. Root elongation rate wasanalysed by considering three terms, (i) the branch appearancerate, (ii) the individual elongation rates of the taproot andbranches and (iii) the proportion of branches which stop elongating.Large ranges ofPPFD and soil temperature were obtained in aseries of field and growth chamber experiments. In the field,the growth of root systems experiencing day-to-day natural fluctuationof PPFD and temperature was followed, and some of the plantsunder study were shaded. In the growth chamber, plants experiencedcontrasting and constant PPFDs and root temperatures. The directeffect of apex temperature on individual root elongation ratewas surprisingly low in the range 13–25C, except forthe first days after germination. Root elongation rate was essentiallyrelated to intercepted PPFD and to distance to the source, bothin the field and in the growth chamber. Branch appearance ratesubstantially varied among days and environmental conditions.It was essentially linked to taproot elongation rate, as theprofile of branch density along the taproot was quite stable.The length of the taproot segment carrying newly appeared brancheson a given day was equal to taproot elongation on this day,plus a 'buffering term' which transiently increased if taprootelongation rate slowed down. The proportion of branches whichstopped elongating a short distance from the taproot rangedfrom 50–80% and was, therefore, a major architecturalvariable, although it is not taken into account in current architecturalmodels. A set of equations accounting for the variabilitiesin elongation rate, branch appearance rate and proportion ofbranches which stop elongating, as a function of interceptedPPFD and apex temperature is proposed. These equations applyfor both field and growth chamber experiments. Key words: Sunflower, root system, model, temperature, radiation     

Possible Mechanism of the Detached Unripe Green Tomato Fruit Turning Red

In general, a mature green tomato will ripen and turn red on the vine or off the vine. Interestingly, an unripe green (UG) tomato also will turn red after being detached from the plant, but the mechanism behind this is unclear. Our study showed that detached UG fruits were able to become red-ripened at the room temperature (25?°C), although fruit quality was lower than that of the vine-ripened fruit. In addition, detached UG fruits exposed to light accumulated more lycopene and total soluble sugars than those incubated in darkness. When the detached UG fruits were stored at a low temperature (10?°C), the fruit-ripening process was nearly blocked, which displayed a non-ripening phenotype. At a high temperature (35?°C), the detached UG fruit showed a yellow-color on ripening, and fruit qualities such as lycopene and soluble sugars were obviously lower than those stored at 25?°C. Moreover, detaching the UG fruit from the plant evoked a rapid increase in total respiration as well as alternative pathway respiration, but ethylene production was not stimulated during the first 24 h of storage. Importantly, the application of nPG, an inhibitor of alternative pathway respiration, markedly suppressed the wound-induced rise in total respiration and delayed the ripening of detached UG fruit. These findings imply that wound-induced respiration might be a signature for launching the onset of the ripening of detached UG fruit, and the optimal conditions of light and temperature are beneficial for the color change and the ripening processes.     

Energy metabolism of Plantago lanceolata, as affected by change in root temperature

The long and short term metabolic effects of a shift in root temperature was investigated in Plantago lanceolata L. with special reference to the role of the cyanide resistant alternative pathway in root respiration. After a 10-day period of growth at a 13°C root temperature, a decrease in root as well as shoot growth was observed, compared to control plants grown continuously at 21°C. Apart from an increase in shoot soluble and insoluble sugar level, no changes in metabolism were found, neither in root respiration, shoot photosynthesis, nor in root sugar and plant protein level.
Decreasing the root temperature from 21 to 13°C gave several clear short term changes in metabolism. Within one hour a decrease in cytochrome chain activity of the roots was found together with an increase in activity of the alternative chain. After 24 h a recovery to the initial level of both chains was observed. An increase in root temperature from 13 to 21°C gave an immediate increase in activity of both respiratory chains that was still present 24 h after the switch.
It is concluded that the activity of the alternative respiratory pathway in the root is strongly affected by a sudden temperature change in the root environment. This pathway acts in a way which is described by 'the energy overflow model'. The presence of the alternative electron transport pathway should be taken into account in determinations of the respiratory Q₁₀. Moreover, the length of time between the temperature change and respiration measurements is an important factor.     

Growth, photosynthesis and respiration in Plantago coronopus as affected by salinity

Plantago coronopus was grown in a non-saline culture solution and in a culture solution containing 50 m M NaCl. The rates of dry matter accumulation in both roots and shoots were not affected by 50 m M NaCl. Photosynthesis, expressed per shoot, was also the same in both environments. Neither the rate of shoot respiration nor that of root respiration was affected by salinity. In both environments the alternative respiratory pathway contributed to the same extent in root respiration. The activity of the alternative pathway decreased with increasing age. Since the respiratory activities were the same in plants grown under both saline and non-saline conditions and since the alternative respiratory pathway was also equally active in roots under both environmental conditions, it is concluded that respiratory costs involved in growth in 50 m M NaCl are negligible in terms of the plant's total energy costings.     

Cytochrome and alternative pathway respiration in white spruce (Picea glauca) roots. Effects of growth and measurement temperature

Interactions between growth temperature and measurement temperature were examined for their effects on white spruce [ Picea glauca (Moench) Voss] root respiration. Total dark respiration rates increased with measurement temperature and were unaffected by growth temperature. Partitioning of respiratory electron flow between the cytochrome and alternative pathways was also unaffected by growth temperature. The proportion of respiration mediated by the alternative pathway was constant at measurement temperatures between 4°C and 18°C, but was increased at higher temperatures. Changes in alternative pathway activity were paralleled by changes in capacity, and the alternative pathway was almost fully engaged at all temperatures. Roots grown at low temperature displayed higher carbohydrate levels than roots grown at higher temperatures, but respiration rate was unaffected. Spruce root respiration did not appear to acclimate to growth temperature, and the alternative pathway was not preferentially engaged at low temperature.     

Seasonal Changes in Molecular Forms of Acid Phosphatase and Ribonuclease of Potato Tubers and the Effects of Infection by Phytophthora erythroseptica

Sequential changes in total activity and molecular forms ofacid phosphatase and ribonuclease from potato tubers were studiedby seasonal assays and Sephadex gel filtration. Ribonucleaseand p-nitrophenyl phosphatase activity fluctuated during storageof tubers, while ß-glycerophosphatase declined toa low level coincident with initiation of sprout growth. Inrecently-lifted tubers acid phosphatase activity occurred ina single high molecular weight peak. Two new forms of lowermolecular weight appeared during ageing of stored tubers. Theinfluence of infection by a tuber-rotting fungus, Phytophthoraerythroseptica,on these seasonal changes was variable. No consistent effectson total hydrolase activities were observed, while post-infectionalchanges in molecular forms included a pronounced shift in themajor acid phosphatase peak. The possible significance of thismolecular weight change in infected samples is discussed inthe light of recent evidence concerning the sub-unit structureof acid phosphatase from potato tubers.     

Alternate Bearing Affects Nitrogen, Phosphorus, Potassium and Starch Storage Pools in Mature Pistachio Trees

The relationship between crop load and the functional storageof selected macronutrients and starch was assessed to developnutrient budgets and best management fertilization practicesin orchards. Functional storage represents the amount of nutrientsand starch redistributed from perennial tree parts in supportof the spring growth flush. Functional storage was influencedby:(a)nutrient and starch accumulation prior to dormancy; and(b)nutrientand starch demand by vegetative and reproductive organs in spring.Lightly cropping (off-year) trees stored 7, 14 and 2 times asmuch N, P and K, respectively, as heavily cropping (on-year)trees. Similar to many biennial plant species, nutrients thataccumulated during the vegetative phase in off-year trees wereused to support reproductive growth during the subsequent on-year.Soil nutrient uptake contributed more to storage pools thanleaf nutrient resorption in off-year-trees, while the reversewas true in on-year trees. Net nutrient resorption from senescingleaves accounted for all of the N and P and a third of the Kstored in on-year trees. Only between 20–33% of the N,P and K stored in perennial tissues of off-year trees couldbe attributed to leaf nutrient resorption. This is the firststudy to determine the amounts of nutrients stored in the perennialparts of mature, field-grown trees and the relative contributionsof leaf nutrient resorption and soil nutrient uptake to functionalstorage in trees.Copyright 1998 Annals of Botany Company Pistacia vera, nutrient storage, biennial bearing, crop load, leaf nutrient resorption, source-sink relationships.     

The Effect of Light Intensity and Relative Humidity on Growth Rate and Root Respiration of Plantago lanceolata and Zea mays

Plants of Plantago lanceolata L. and Zea mays L., cv. ‘Campo’were grown at two levels of light intensity. Especially in theroots, the rate of dry matter accumulation decreased at lowlight intensity. The carbohydrate content of both roots andshoots of P. lanceolata was not affected by light intensity.The relative contribution of SHAM¹-sensitive respiration, thealternative chain, to total root respiration of both P. lanceolataand Z. mays, was not affected by light intensity during thedaytime. The alternative pathway was somewhat decreased at theend of the dark period, but not in the root tips (0–5mm) where it still contributed 56% in respiration. It was, therefore,concluded that photosynthesis is not a major factor in regulationof root growth in the species investigated. To see whether the effect of light intensity on root growthrate was via transpiration, plants of Z. mays were grown atdifferent air humidities. Both high humidity and low light intensityaffected the root morphology in such a way that the distancebetween the apex and the first laterals on the primary rootaxis increased. It is suggested that this effect on root morphologyis due to transpiration and the subsequent removal of root-producedinhibitors of lateral root growth; although light intensityalso affected the rate of dry matter accumulation of roots andthe rate was not affected by the humidity of the air. It is,therefore, concluded that the effect of light intensity on therate of dry matter accumulation of roots of Z. mays is not viaan effect on transpiration.     

Carbon Economy of Carrots During Initiation of the Storage Root in Cultivars Contrasting in Shoot: Root Ratio at Maturity

Photosynthesis, respiration and growth of two cultivars of carrotwith contrasting ratios of shoot: storage root weight at maturity,were compared during initiation of the storage root at 20 °C.Partition of assimilate between shoot, roots and respirationshowed no varietal differences but distribution between storageand fibrous roots was different from the time that the storageroot could be morphologically identified. For both cultivarsover the period investigated, approximately 64% of net photosynthesiswas partitioned to the shoot with 5% lost as respiration duringthe dark and 59% used in growth. Of that exported to the rootsystem (36%), 19% (of net photosynthesis) was used in growthand 17% was lost in respiration. In the cultivar with greatershoot: storage root ratio at maturity, 4.6% was allocated tothe storage root in contrast to 7.5% in the cultivar with alesser shoot: storage ratio at maturity. It is concluded thatgreater dry matter accumulation in the storage root of the lattercultivar does not result from transient differences in respiratoryloss and is not evident in shoot to total root dry matter distributionover this period. Daucus carota L, carrot, assimilate partition, shoot, storage root, shoot: root ratio     

Root Respiration and Carbohydrate Status of Two Wheat Genotypes in Response to Hypoxia

To investigate root respiration and carbohydrate status in relationto waterlogging or hypoxia tolerance, root respiration rateand concentrations of soluble sugars in leaves and roots weredetermined for two wheat (Triticum aestivum L.) genotypes differingin waterlogging-tolerance under hypoxia (5% O₂) and subsequentresumption of full aeration. Root and shoot growth were reducedby hypoxia to a larger extent for waterlogging-sensitive Coker9835. Root respiration or oxygen consumption rate declined withhypoxia, but recovered after 7 d of resumption of aeration.Respiration rate was greater for sensitive Coker 9835 than fortolerant Jackson within 8 d after hypoxia. The concentrationsof sucrose, glucose and fructose decreased in leaves for bothgenotypes under hypoxia. The concentration of these sugars inroots, however, increased under hypoxia, to a greater degreefor Jackson. An increase in the ratio of root sugar concentrationto shoot sugar concentration was found for Jackson under hypoxicconditions, suggesting that a large amount of carbohydrate waspartitioned to roots under hypoxia. The results indicated thatroot carbohydrate supply was not a limiting factor for rootgrowth and respiration under hypoxia. Plant tolerance to waterloggingof hypoxia appeared to be associated with low root respirationor oxygen consumption rate and high sugar accumulation underhypoxic conditions.Copyright 1995, 1999 Academic Press Oxygen consumption rate, sugar accumulation, Triticum aestivum L., waterlogging tolerance     

Comparative Enzymic Studies of Sucrose Metabolism in the Taproots and Fibrous Roots of Beta vulgaris L

Comparative enzymic studies of sugar beet (Beta vulgaris L.) taproots and fibrous roots revealed differences in invertase (EC 3.2.1.26) and sucrose synthetase (EC 2.4.1.13) activity. Invertase activity of the two root forms differs with respect to specific activity, pH optimum, and enzyme solubility. Acid invertase (pH 4.5) in the taproot was restricted to the peripheral meristematic tissue which produces cells for both taproot and fibrous root growth. This finding supports the hypothesis that the enzyme regulates sucrose partitioning between the taproot and fibrous roots. A distinct alkaline invertase (pH 8.0) was detected in sucrose storage tissues of the taproot.     

Responses of young trees to wind and shading: effects on root architecture

Two wind tunnels were designed to detect influences of windon the development of the root systems of young trees: Piceasitchensis and Larix decidua were grown in the first and L.decidua only in the second. In the second experiment, the taproot of each L. decidua seedling was removed in order to mimicthe formation of a shallow root-plate. Responses of shoot growthto wind stress were small, although uneven irradiance levelsresulted in asymmetric growth of both shoots and roots; thedistribution of root biomass around the tree was related spatiallyto that of shoot growth In both experiments there was an increase in the number of largewindward and leeward roots in both species. In the first experiment,the sum of the crosssectional area (     

Interactions between osmoregulation and the alternative respiratory pathway in Plantago coronopus as affected by salinity

Plantago coronopus L., a species from the coastal zone, was grown in culture solution with and without 50 mM NaCl. In addition it was transferred from a non-saline solution to a solution containing 50 mM NaCl. Short term effects of NaCl on growth and various aspects of energy metabolism, including photosynthesis, shoot dark respiration, root respiration and the contribution of the SHAM-sensitive alternative pathway to root respiration were investigated. The concentrations of soluble and insoluble non-structural carbohydrates and of sorbitol a compatible osmotic solute in Plantago, in both shoots and roots were also determined. Growth of shoots and roots was largely unaffected by addition of 50 mM NaCl. Net photosynthesis, shoot dark respiration and the concentration of non-structural carbohydrates in both shoots and roots were also unaffected by salinity. The rate of root respiration immediately decreased upon addition of 50 mM NaCl. This decrease was almost exclusively attributed to a decreased activity of the SHAM-sensitive alternative pathway. The concentration of sorbitol in the roots increased quickly after addition of 50 mM NaCl, whilst the increase in sorbitol concentration in the shoots started later. The time course of the increase of sorbitol concentration was similar to that of the decrease in activity of the alternative pathway. During the first 12 h after exposure to 50 mM NaCl, the amount of carbohydrates which was saved in respiration, due to the decreased activity of the alternative pathway, was the same as that used for sorbitol synthesis in the roots. It is concluded that the activity of the alternative pathway decreased due to increased utilization of carbohydrates for sorbitol synthesis, according to a proposed ‘energy overflow model’. After 24 h, the sorbitol concentration in the cytoplasm of the root cells of plants transferred to a saline solution reached a level that was sufficient to compensate for 50 mM NaCl, assuming a cytoplasmic volume of ca. 10% of the total cell volume. The sorbitol concentration in roots of plants grown in a saline environment for several weeks was lower than that in roots of plants transferred to a saline environment for c. 24 h. It is suggested that sorbitol accumulated in roots of Plantago coronopus as an immediate reaction upon salinity, whilst other adaptations may occur thereafter.     

Patterns of Root Respiration Associated with the Induction of Aluminium Tolerance in Phaseolus vulgaris L.

Aluminium (Al) tolerance in an Al-tolerant cultivar of Phaseolusvulgaris L. (‘Dade’) was found to be an inducibletrait. Upon exposure to 10 µM Al, the rate of root elongationwas inhibited in comparison to controls. During the following72 h, the rate of elongation returned to levels comparable tocontrols. In contrast, root elongation of an Al-sensitive cultivar(‘Romano’) did not recover after exposure to Al.In Dade, the resumption of root elongation following exposureto Al was accompanied by increased rates of root respiration,whereas respiration rates slowly declined over the 72 h treatmentperiod in Romano. When partitioned into growth and maintenanceexpenditures, a larger proportion of root respiration of Dadeexposed to Al was allocated to maintenance processes, potentiallyreflecting diversion of energy to metabolic pathways that offsetthe adverse effects of Al toxicity. Romano did not show sucha pattern and respiration associated with both growth and maintenancewas reduced after exposure to Al. Root and shoot growth of bothcultivars were also measured to determine the effects of long-term(21 d) exposure to 10 µM Al. Dade plants exposed to Alexhibited enhanced growth in comparison to controls, whereasRomano plants were characterized by reduced shoot and root growth.Modelling the time-course of root respiration and measuringthe long-term growth responses to Al is a valuable method ofelucidating respiratory costs of stress tolerance. Key words: Aluminium, differential tolerance, maintenance respiration, Phaseolus vulgaris, root respiration     

Efficiency of Root Respiration in Relation to Growth Rate, Morphology and Soil Composition

Root growth respiration and root maintenance respiration rate of the following species were determined: Hypochaeris radicata L. ssp. radicata L., H. radicata ssp. ericetorum Van Soest, Plantago lanceolata L., P. major L. ssp. major, P. major ssp. pleiosperma Pilgcr, P. maritime L., Senecio viscosus L., S. vulgaris L. and Urtica dioica L. A high root growth respiration (i.e. the amount of oxygen consumed for synthesis of a given weight of root material) implied a high maintenance respiration rate (i.e. the amount of oxygen consumed per unit of time and dry weight, but not connected with growth). High values of both components reflect a low efficiency of root respiratory processes. The efficiency of root respiration, as determined by the values for root growth respiration and root maintenance respiration rate could not be demonstrated to be of advantage in adaptation to soil conditions, as e.g. nitrogen content, moisture content and pH. It is concluded that (he degree of ‘wasteful utilization of sugars’ in roots, i.e. such consumption of sugars as cannot be related to structural growth, storage of carbohydrates or maintenance processes, depends on imbalance of transport of sugars from the shoot to the roots with utilization of sugars for synthesis of root material. The results are discussed in relation to Brouwer's explanation for the equilibrium between the growth of shoots and of roots. Root growth rate in the present species appears limited by a factor produced in the shoot under light conditions, and which factor is distinct from carbohydrates. The evidence presented shows that relatively inefficient root respiration does not imply a low growth rate. In regulation of plant growth the growth rate itself and also the shoot to-root ratio may be more important than the regulation of the efficiency of energy metabolism.     

Respiration in postharvest sugarbeet roots is not limited by respiratory capacity or adenylates

Control of respiration has largely been studied with growing and/or photosynthetic tissues or organs, but has rarely been examined in harvested and stored plant products. As nongrowing, heterotrophic organs that are reliant on respiration to provide all of their metabolic needs, harvested plant products differ dramatically in their metabolism and respiratory needs from growing and photosynthetically active plant organs, and it cannot be assumed that the same mechanism controls respiration in both actively growing and harvested plant organs. To elucidate mechanisms of respiratory control for a harvested and stored plant product, sugarbeet (Beta vulgaris L.) root respiration was characterized with respect to respiratory capacity, adenylate levels and cellular energy status in roots whose respiration was altered by wounding or cold treatment (1 degrees C) and in response to potential effectors of respiration. Respiration rate was induced by wounding in roots stored at 10 degrees C and by cold temperature in roots stored at 1 degrees C for 11-13d. Alterations in respiration rate due to wounding or storage temperature were unrelated to changes in total respiratory capacity, the capacities of the cytochrome c oxidase (COX) or alternative oxidase (AOX) pathways, adenylate concentrations or cellular energy status, measured by the ATP:ADP ratio. In root tissue, respiration was induced by exogenous NADH indicating that respiratory capacity was capable of oxidizing additional electrons fed into the electron transport chain via an external NADH dehydrogenase. Respiration was not induced by addition of ADP or a respiratory uncoupler. These results suggest that respiration rate in stored sugarbeet roots is not limited by respiratory capacity, ADP availability or cellular energy status. Since respiration in plants can be regulated by substrate availability, respiratory capacity or energy status, it is likely that a substrate, other than ADP, limits respiration in stored sugarbeet roots.     

MassFlowDyn I: A Carbon Transport and Partitioning Model for Root System Architecture

Carbon partitioning is important for understanding root developmentbut little is known about its regulation. Existing models suggestthat partitioning is controlled by the potential sink strength.They cannot, however, simulate hierarchical uptake other thanby using absolute priorities. Moreover, they cannot explainthat the changes in photoassimilate partitioning result fromchanges in photosynthesis. In this paper we present a modelof phloem sieve circulation, based on the model of Minchin etal. (Journal of Experimental Botany44: 947–955, 1993).The root system was represented by a network of segments towhich meristems were connected. The properties of the segmentswere determined by the differentiation stage. Photoassimilateimport from each organ was assumed to be limited by a metabolicprocess and driven by Michaelis–Menten kinetics. The axialgrowth was proportional to meristem respiration, which drivesthe flux of new cells required for root elongation. We usedthe model to look at trophic apical dominance, determinate andindeterminate root growth, the effect of the activity of a rooton competition with its neighbours, and the effect of photoassimilateavailability on changes in partitioning. The simulated phloemmass flow yielded results of the same order of magnitude asthose generally reported in the literature. For the main wellvascularized axis, the model predicted that one single apicalmeristem larger than its neighbouring laterals, was enough togenerate a taprooted system. Conversely, when the meristem oflaterals close to the collar had a volume similar to that ofthe taproot, the predicted network became fibrous. The modelpredicted a hierarchical priority for organ photoassimilateuptake, similar to that described in the literature, duringthe decline in photosynthetic activity. Our model suggests thatdeterminate growth of the first laterals resulted from a localshortage of photoassimilate at their meristem, as a result ofthe limited transport properties of the developed roots. Copyright2000 Annals of Botany Company Münch theory, phloem transport model, photoassimilate-partitioning, root growth, root system architecture, translocation