Sectoriality and physiological organisation in herbaceous plants: an overview

The physiological organisation of plants is considered in relation to the carbon economy of plant parts. Although assimilate is partitioned according to the relative strength of sinks, in many species there is also a very close relationship between partitioning and shoot phyllotaxy, giving rise to sectorial patterns of allocation whereby only certain sinks are supported by any source leaf. Essentially these sinks are in the same orthostichy as the source leaf. This constraint of the vascular architecture on assimilate distribution to developing sinks such as leaves, flowers and fruits is not always absolute, as following the loss of their principal source leaves these sinks can in many cases be supplied with assimilate by other leaves via new inter-orthostichy pathways. The supply of assimilate to major sinks such as developing fruits becomes more and more localised with time so that a fruit in an axillary position becomes largely supported by its subtending leaf; the reproductive node—a metamer-can thus be regarded as a relatively autonomous unit of the plant (an IPU). Similary, once established after a developmental phase of assimilate import, tiller ramets and branches in unitary plants tend to become physiologically autonomous modules. However, the functional autonomy of tillers is reversed following defoliation or shading as they are then sustained by the import of assimilate, subject to its availability, from unaffected tillers. Consequently the plant becomes physiologically integrated by the flow of assimilate from one part to another. The mainly autonomous ramets of many stoloniferous and rhizomatous species display a similar pattern of physiological integration in response to source manipulation, but in some species the ramets appear to maintain their independent functioning as a normal feature of the carbon allocation within the clone. In other clonal species, as the clone develops and becomes more structurally complex, vascular constraints start to restrict the movement of resources, and the clone becomes composed of a number of semi-autonomous IPUs. In unitary plants branches appear to remain very physiologically isolated in terms of their carbon economy once they become established, irrespective of a range of source-sink manipulations.These different patterns of physiological integration and organisation are discussed in relation to different strategies of assimilate utilisation and conservation.     

Plants as resource mosaics: a functional model for predicting patterns of within-plant resource heterogeneity to consumers based on vascular architecture and local environmental variability

Plant characteristics that determine food quantity and quality to consumers exhibit extensive within-plant heterogeneity, and this heterogeneity is an important influence on the interactions between plants and consumers (herbivores, pathogens, mutualists, soil-dwelling microorganisms). Here we present a functional model – based on plant vascular architecture and local environmental variability – that can be used to predict the patterns of within-plant resource heterogeneity. We argue that heterogeneity is generated largely by sectoriality, the restricted movement of resources along vascular traces within a plant. In essence, the combination of sectoriality and spatial variation in previous damage, nutrient, water, and light availability generates predictable patterns of within-plant heterogeneity in tissue quality. We point out that vascular architecture differs across taxa, growth habit and plant developmental stage, and suggest that certain attributes of the environment maximize the extent of heterogeneity.     

Vascular architecture and patchy nutrient availability generate within-plant heterogeneity in plant traits important to herbivores

Within-plant heterogeneity in growth, morphology, and chemistry is ubiquitous, and is commonly attributed to differences in tissue age, light availability, or previous damage by herbivores. Although these factors are important, we argue that plant vascular architecture is an underappreciated determinant of heterogeneity. Vascular architecture can restrict the transport of resources (nutrients, photosynthate, hormones, etc.) to within specific sectors of the plant: this is referred to as sectoriality. Although studies have documented sectoriality in the transport of isotopes and dyes from roots to shoots, the ecological consequences of this sectoriality remain poorly understood. We tested the hypothesis that spatial variation in belowground nutrient availability combined with sectorial transport results in localized "fertilization" of aboveground plant parts and generates heterogeneity in traits important to herbivores. Our split-root experiments with tomato (Lycopersicon esculentum Mill) clearly demonstrate that fertilization to isolated lateral roots generates heterogeneity in leaf morphology, phenolic chemistry, and side-shoot growth. Specifically, leaflets with direct connections to these lateral roots were larger and had lower levels of rutin and chlorogenic acid than did leaflets in other sectors lacking direct vascular connections. Moreover, side-shoot production was greater in the connected sectors. We discuss the implications of this heterogeneity for plant-herbivore interactions.     

Vascular pathways constrain 13C accumulation in large root sinks of Lycopersicon esculentum (Solanaceae)

While carbon transport and partitioning is largely determined by phloem source-sink relationships, it may be constrained by vascular connections. Tomato (Lycopersicon esculentum) plants exhibit a high degree of sectoriality, with restricted movement of nutrients from particular roots to orthostichous leaves. In this experiment we investigated the manner in which sectoriality influences source-sink phloem partitioning from shoots to roots in tomatoes and whether the size of the sink (root) modifies the pattern of carbon movement outside sectored pathways. Using (13)C, we determined that shoot-to-root carbon transport in tomatoes is sectored even from upper leaves. Sink size also influenced carbon partitioning. Specifically, when a lateral root was grown in isolation (using a split-pot technique), it grew more and acquired significantly more (13)C from an orthostichous, exposed leaf than did any other single root. Vascular constraints were evident. (13)C accumulation in a large, isolated lateral root was very low when a leaf opposite the isolated lateral root was exposed. Thus sink size did not overcome vascular constraints. Because carbon assimilates are needed for nutrient acquisition and assimilation, these vascular constraints may affect the ability of sectored plants to utilize heterogeneously distributed soil resources. If so, future studies should compare species that differ in sectoriality to determine whether vascular constraints affect competitive hierarchies when soil resource availability is patchy.     

Causes and consequences of sectoriality in the clonal herb Glechoma hederacea

The causes of sectoriality and consequences for clone behaviour are examined using data from the stoloniferous herb Glechoma hederacea. The proximal causes of physiological integration patterns are investigated using anatomical studies, acid fuchsin dye to reveal patterns of xylem continuity between ramets, and ¹⁴C as a label to reveal quantitative photoassimilate translocation patterns in the phloem. Dye movement in the xylem was acropetal and sectorial, and the sectoriality was determined by phyllotaxy. Patterns of ¹⁴C-labelled photoassimilate allocation were qualitatively similar to those of xylem based resources, although there was some basipetal movement of photoassimilate. The patterns of physiological integration and independence between ramets are shown to be governed by rules which depend on vascular continuity and discontinuity between ramets. Physiological support to stolon apices results in acquisition of relative branch autonomy (branches become semi-autonomous integrated physiological units, IPUs).This paper evaluates whether observed physiological integration patterns may be modified by altering normal source-sink relationships or by modifying environmental conditions. An experiment using different defoliation intensities, and different defoliation patterns at the same overall intensity, demonstrated that the precise positions of leaves removed from a clone had unique consequences for its subsequent development. Individual ramets of a given clone may be located in microhabitats of differing quality. An experiment in which competition was either present or absent throughout the space occupied by the clone, or patchy in distribution, showed that G. hederacea did not respond to competition at the whole clone level. Instead, connected stolons (IPUs) responded independently to local competition. Sectoriality may promote the restriction of lethal, localised environmental factors within the affected IPU. A study investigating the uptake and translocation of zinc by clones revealed that quantified patterns of zinc distribution resembled patterns of ¹⁴C movement in the phloem, and that there was no significant transport of zinc from one stolon to another.Although sectorial patterns of resource movement in G. hederacea can be modified in the short term, in the long-term, physiological integration may not allow this species to integrate the effects of environmental heterogeneity. A mobile clonal species with a high growth rate and relatively short-lived ramets, such as G. hederacea, is likely to benefit from a semi-autonomous response to patch quality at the level of the stolon, since the alternative of widespread intra-clonal support may increase the residence time of the clone in unfavourable pathches.     

The heterogeneity of the plasma membrane H+-ATPase response to auxin

The sensitivity of the plasma membrane H⁺-ATPase in tobacco was investigated in vitro, both at the proton translocation level and the ATPase level, according to plant development and leaf location. Both activities are stimulated by auxin in all leaves, whatever the plant age and the leaf age. However, the sensitivity to auxin was heterogeneous with respect to plant development and leaf location. In parallel experiments using the same plasma membrane samples, polypepides patterns were investigated by two-dimensional gel electrophoresis and image analysis was used to quantify the relative abundance of 110 peptides. Systematic analysis of the two kinds of data identified 8 polypeptides, the abundance of which changed in a consistent way with the sensitivity, whatever the plant developmental state and leaf location. These unknown polypeptides are proposed as potential markers of the membrane response to auxin.     

Carbon balance of a whole tomato plant and the contribution of source leaves to sink growth using the 14CO2 steady-state feeding method

To clarify the entire carbon balance of a young tomato plant and the contribution of each leaf to sink growth, the carbon balance of each leaf was quantitatively measured using the 14CO₂ steady-state feeding method to quantitatively measure the photosynthesis, translocation, distribution and respiration of newly fixed 14C. The entire carbon balance of the whole plant was calculated by adding the data of each leaf. The total amount of carbon fixed by all source leaves was 70.2 mg. Of this amount, in a 24-h period, 29% was accumulated in the sinks, 28% remained in the source leaves and 42% was respired. Of the total amount of carbon accumulated in the sinks, the proportion accumulated in the shoot apex, stem and roots were 27, 40 and 29%, respectively. The third and fourth leaves contributed about 30–40% of the total growth of the main sinks. The distribution pattern of each leaf to the shoot apex of the plant was greatest in the first leaf and decreased with decreasing leaf age, whereas it showed an opposite trend in the roots.     

How are leaves plumbed inside a branch? Differences in leaf-to-leaf hydraulic sectoriality among six temperate tree species

The transport of water, sugar, and nutrients in trees is restricted to specific vascular pathways, and thus organs may be relatively isolated from one another (i.e. sectored). Strongly sectored leaf-to-leaf pathways have been shown for the transport of sugar and signal molecules within a shoot, but not previously for water transport. The hydraulic sectoriality of leaf-to-leaf pathways was determined for current year shoots of six temperate deciduous tree species (three ring-porous: Castanea dentata, Fraxinus americana, and Quercus rubra, and three diffuse-porous: Acer saccharum, Betula papyrifera, and Liriodendron tulipifera). Hydraulic sectoriality was determined using dye staining and a hydraulic method. In the dye method, leaf blades were removed and dye was forced into the most proximal petiole. For each petiole the vascular traces that were shared with the proximal petiole were counted. For other shoots, measurements were made of the leaf-area-specific hydraulic conductivity for the leaf-to-leaf pathways (k(LL)). In five out of the six species, patterns of sectoriality reflected phyllotaxy; both the sharing of vascular bundles between leaves and k(LL) were higher for orthostichous than non-orthostichous leaf pairs. For each species, leaf-to-leaf sectoriality was determined as the proportional differences between non-orthostichous versus orthostichous leaf pairs in their staining of shared vascular bundles and in their k(LL); for the six species these two indices of sectoriality were strongly correlated (R2=0.94; P <0.002). Species varied 8-fold in their k(LL)-based sectoriality, and ring-porous species were more sectored than diffuse-porous species. Differential leaf-to-leaf sectoriality has implications for species-specific co-ordination of leaf gas exchange and water relations within a branch, especially during fluctuations in irradiance and water and nutrient availability.     

Leaf evolution: gases, genes and geochemistry

AIMS: This Botanical Briefing reviews how the integration of palaeontology, geochemistry and developmental biology is providing a new mechanistic framework for interpreting the 40- to 50-million-year gap between the origination of vascular land plants and the advent of large (megaphyll) leaves, a long-standing puzzle in evolutionary biology. SCOPE: Molecular genetics indicates that the developmental mechanisms required for leaf production in vascular plants were recruited long before the advent of large megaphylls. According to theory, this morphogenetic potential was only realized as the concentration of atmospheric CO2 declined during the late Palaeozoic. Surprisingly, plants effectively policed their own evolution since the decrease in CO2 was brought about as terrestrial floras evolved accelerating the rate of silicate rock weathering and enhancing sedimentary organic carbon burial, both of which are long-term sinks for CO2. CONCLUSIONS: The recognition that plant evolution responds to and influences CO(2) over millions of years reveals the existence of an intricate web of vegetation feedbacks regulating the long-term carbon cycle. Several of these feedbacks destabilized CO2 and climate during the late Palaeozoic but appear to have quickened the pace of terrestrial plant and animal evolution at that time.     

Plant architecture, sectoriality and plant tolerance to herbivores

The evolution of tolerance is one potential plant response to selection imposed by herbivores. Plant architecture, and in turn, sectoriality may influence a plant's ability to tolerate tissue loss. However, each may either constrain or facilitate a plant's ability to compensate following herbivore attack depending on the plant part damaged and the identity of the damaging herbivore.Plants are limited in their ability to respond to localized damage by chewing insects because carbon does not flow freely from damaged to undamaged plant parts, particularly between branches. Thus, defoliation of individual branches invariably results in decreased growth and reproduction of those branches. Within branches, carbon flow via vascular connections between orthostichies may ameliorate the effects of damage restricted within an orthostichy. Local induction of secondary chemicals to spread damage by folivores throughout a plant's canopy, redistribution of resources within and between IPU's, and delaying reproductive activity until resources have been pooled may all alleviate the constraints on response of plants to grazing.In contrast to the effects of damage by grazers, the metameric construction of plants typically ensures points of regrowth from dormant buds when apical meristems are destroyed either by vertebrate browsers or galling insects. Sectoriality constrains the ability of sap-sucking insects to tap the entire resource base of a plant, thus having a positive effect on plant fitness. However, both the site and timing of attack mitigate the degree of limitation imposed by sectoriality. During peak periods of assimilation, photosynthate flow is mainly over short distances (between sources and sinks within the canopy), and thus sap-sucking insects have a small resource base to draw upon. In contrast, when sucking insects tap into vascular elements in which the flow is from roots to leaves and vice versa, resource availability to the insect (and in turn, potential resource loss from the plant) are only limited by the resources present in those vascular elements.Studies of specific traits in species which demonstrate differential tolerance would greatly add to our understanding of herbivore impacts on plant growth and reproduction. In particular, intraspecific variation in tolerance has been documented for individuals within and among populations with different grazing histories. A number of traits related to sectoriality and architecture probably contribute to such variation in tolerance, and because they are easily manipulated and easily quantified, represent potentially profitable avenues of research. These traits include distribution of leaves and buds, ability to release secondary meristems from dormancy, and the timing of resource movement both before and subsequent to damage.     

Carbon Sink-to-Source Transition Is Coordinated with Establishment of Cell-Specific Gene Expression in a C4 Plant

Plants that use the highly efficient C4 photosynthetic pathway possess two types of specialized leaf cells, the mesophyll and bundle sheath. In mature C4 leaves, the CO2 fixation enzyme ribulose-1,5-bisphosphate carboxylase (RuBPCase) is specifically compartmentalized to the bundle sheath cells. However, in very young leaves of amaranth, a dicotyledonous C4 plant, genes encoding the large subunit and small subunit of RuBPCase are initially expressed in both photosynthetic cell types. We show here that the RuBPCase mRNAs and proteins become specifically localized to leaf bundle sheath cells during the developmental transition of the leaf from carbon sink to carbon source. Bundle sheath cell-specific expression of RuBPCase genes and the sink-to-source transition began initially at the leaf apex and progressed rapidly and coordinately toward the leaf base. These findings demonstrated that two developmental transitions, the change in photoassimilate transport status and the establishment of bundle sheath cell-specific RuBPCase gene expression, are tightly coordinated during C4 leaf development. This correlation suggests that processes associated with the accumulation and transport of photosynthetic compounds may influence patterns of photosynthetic gene expression in C4 plants.     

Elevated CO2 and plant structure: a review

Consequences of increasing atmospheric CO₂ concentration on plant structure, an important determinant of physiological and competitive success, have not received sufficient attention in the literature. Understanding how increasing carbon input will influence plant developmental processes, and resultant form, will help bridge the gap between physiological response and ecosystem level phenomena. Growth in elevated CO₂ alters plant structure through its effects on both primary and secondary meristems of shoots and roots. Although not well established, a review of the literature suggests that cell division, cell expansion, and cell patterning may be affected, driven mainly by increased substrate (sucrose) availability and perhaps also by differential expression of genes involved in cell cycling (e.g. cyclins) or cell expansion (e.g. xyloglucan endotransglycosylase). Few studies, however, have attempted to elucidate the mechanistic basis for increased growth at the cellular level. Regardless of specific mechanisms involved, plant leaf size and anatomy are often altered by growth in elevated CO₂, but the magnitude of these changes, which often decreases as leaves mature, hinges upon plant genetic plasticity, nutrient availability, temperature, and phenology. Increased leaf growth results more often from increased cell expansion rather than increased division. Leaves of crop species exhibit greater increases in leaf thickness than do leaves of wild species. Increased mesophyll and vascular tissue cross-sectional areas, important determinates of photosynthetic rates and assimilate transport capacity, are often reported. Few studies, however, have quantified characteristics more reflective of leaf function such as spatial relationships among chlorenchyma cells (size, orientation, and surface area), intercellular spaces, and conductive tissue. Greater leaf size and/or more leaves per plant are often noted; plants grown in elevated CO₂ exhibited increased leaf area per plant in 66% of studies, compared to 28% of observations reporting no change, and 6% reported a decrease in whole plant leaf area. This resulted in an average net increase in leaf area per plant of 24%. Crop species showed the greatest average increase in whole plant leaf area (+ 37%) compared to tree species (+ 14%) and wild, nonwoody species (+ 15%). Conversely, tree species and wild, nontrees showed the greatest reduction in specific leaf area (– 14% and – 20%) compared to crop plants (– 6%). Alterations in developmental processes at the shoot apex and within the vascular cambium contributed to increased plant height, altered branching characteristics, and increased stem diameters. The ratio of internode length to node number often increased, but the length and sometimes the number of branches per node was greater, suggesting reduced apical dominance. Data concerning effects of elevated CO₂ on stem/branch anatomy, vital for understanding potential shifts in functional relationships of leaves with stems, roots with stems, and leaves with roots, are too few to make generalizations. Growth in elevated CO₂ typically leads to increased root length, diameter, and altered branching patterns. Altered branching characteristics in both shoots and roots may impact competitive relationships above and below the ground. Understanding how increased carbon assimilation affects growth processes (cell division, cell expansion, and cell patterning) will facilitate a better understanding of how plant form will change as atmospheric CO₂ increases. Knowing how basic growth processes respond to increased carbon inputs may also provide a mechanistic basis for the differential phenotypic plasticity exhibited by different plant species/functional types to elevated CO₂.     

The Influence of Leaf Position and Defoliation on the Assimilation and Translocation of Carbon in White Clover (Trifolium repens L.) 1. Carbon Distribution Patterns

The assimilation of carbon (C) by, and distribution of ¹⁴C from,leaves at each end of an unbroken sequence of ten mature leaveson the main stolon of clonal plants of white clover (Trifoliumrepens L.) were measured to identify intra-plant factors determiningthe direction of C movement from leaves. Leaves at two intermediatepositions were also measured. Localized movement of ¹⁴C to sinks at the same node as, or atthe one to two nodes immediately behind, the fed leaf accountedfor 40–50% of the total ¹⁴C exported by all measured leaves.A further 50–60% of exported ¹⁴C was therefore availablefor more-distant sinks, and the direction of translocation ofthis C was determined by the relative total strength or demand(number x size x rate of activity or growth) of sinks forwardof, or behind, the leaf in question. Thus 85% of the ¹⁴C exportedfrom the youngest measured leaf moved toward the base of thestolon, while about 60% of the ¹⁴C exported from the oldestleaf moved acropetally. Defoliating plants to leave just one mature leaf on the mainstolon (at any one of the same four positions studied in undefoliatedplants), and no leaves on branches, resulted in: (1) increasednet photosynthetic rate in all residual leaves: (2) increased%export of fixed C from one of the four leaves; (3) increasedexport to the main stolon apex from all except the eldest leaf;(4) increased export to branches from three of the four leaves;and (5) decreased export to stolon tissue and roots from allleaves, within 3 d of defoliation. These responses would seemto ensure the fastest possible replacement of lost leaf areaand, thus, restoration of homeostatic growth. The observed patternsof C assimilation and distribution in both undefoliated anddefoliated white clover plants are consistent with the generalrules of source-sink theory; the distance between sources andcompeting sinks, and relative sink strength, emerge as the mostimportant intra-plant factors governing C movement. These resultsemphasize the need to consider plant morphology, and the modularnature of plant growth, when interpreting patterns of resourceallocation in clonal plants, or plant responses to stressessuch as partial defoliation. Trifolium repens L, white clover, photosynthesis, assimilate translocation, defoliation     

Translocation of labelled assimilates following photosynthesis of 14CO2 by the field bean, Vicia faba

When whole plants were exposed to ¹⁴CO₂, almost the same amount of radioactivity was taken up initially by each leaf regardless of its position on the stem and of the presence of beans at that node. Thus, although developing beans are a powerful sink for assimilated carbon, they do not increase the CO₂ uptake by adjoining leaves.
The distribution of labelled assimilates 6 hours after feeding ¹⁴CO₂ to a single leaf for 1 hour varied with both the position of the treated leaf and the stage of development of the plant. Before any flowers were set most of the radioactivity from all expanded leaves moved downwards to the roots and the stem below the treated leaf (lower stem). Later, during pod-fill, the upper leaves maintained this supply to the roots and lower stem, whilst most of the carbon translocated from the lower and mid-stem leaves went to the beans. However, we found no exclusive relationship between a leaf and the supply to beans developing on the same node.
The amount of radioactivity moving out of a source leaf at a fruiting node increased over successive samplings up to 48 h; the pattern of distribution of the ¹⁴CO₂ however remained virtually unchanged.     

On plant sectoriality, or how to combine the benefits of autonomy and integration

Plant sectoriality implies physiological subdivision of physically coherent plant structures. It is largely determined by vascular structure. Sectorial transport of carbon assimilates, mineral nutrients, water or hormones may be an essential component of plant phenotype in ecological interactions. Most studies of sectoriality have focussed on its effects on plant growth, resource allocation and herbivory. Since sectoriality allows semiautonomous reactions to environmental stimuli to be displayed by different plant parts, it also needs to be considered in discussions of selfishness vs. altruism of plant parts. Future lines of research should include analysis of the genetic basis of sectoriality, investigations into root sectoriality and its effects, studies of the impacts of sectoriality on plant life histories, and analyses of intra- and interpopulation variation in traits related to sectoriality.     

Alfalfa physiological response to potato leafhopper injury depends on leafhopper and alfalfa developmental stage

We examined the effects of potato leafhopper (Empoasca fabae) developmental stage and alfalfa (Medicago sativa) developmental stage on the physiological response of the plant to injury. We used radioactive carbon dioxide to label the photoassimilate stream and evaluate the phloem health of alfalfa. In one experiment, six first instar, four fourth instar, and three adult leafhoppers were caged by stage on single alfalfa stems for approximately one day. Only fourth instar nymphs significantly reduced the amount of label transported to injured tissues above the source of the labeled assimilate. First instar nymphs had no effect and adults reduced assimilate transport to stem tips, but this trend was not significant possibly because of confounding variables. However, injury by both first instar nymphs and adults resulted in greater concentration of labeled assimilate in portions of the stem below the feeding site. In another experiment, the developmental stage of alfalfa stems was central to the physiological response of alfalfa to leafhopper injury. A 20 h exposure to three adult leafhoppers significantly reduced the amount of label translocated to the tip and crown tissues of early vegetative plants, and to the crown tissue only of late vegetative plants. In reproductive plants, assimilate translocation was not affected by leafhopper injury. In a final experiment, we found no evidence of an effect on the photosynthesis of leaves of similar age and position to those used as source leaves in our translocation studies. Our findings contribute to our understanding of the physiological response of plants to injury by sap-feeding insects, and suggest the need for greater refinement of economic injury levels based on leafhopper and plant developmental stage.     

Changes in Nonstructural Carbohydrates in Different Parts of Soybean (Glycine max [L.] Merr.) Plants during a Light/Dark Cycle and in Extended Darkness

Diurnal patterns of nonstructural carbohydrate (starch, sucrose, and hexose sugars) concentration were characterized in different parts (leaves, petioles, stems, and roots) of vegetative soybean (Glycine max [L.] Merr.) plants. Pronounced changes in all carbohydrate pools were observed in all plant parts during the normal photosynthetic period; however, starch accumulation within leaves accounted for more than 80% of the nonstructural carbohydrate accumulated by the plant during the light period. Efficiency of utilization of starch and sucrose during the normal dark period differed among organs, with leaves being most efficient in mobilizing starch reserves and roots being most efficient in utilizing sucrose reserves. The vast majority (about 85%) of the whole plant carbohydrate reserves present at the end of the photosynthetic period were utilized during the normal dark period. Sink leaf expansion ceased in plants transferred to extended darkness and the cessation in leaf expansion corresponded with carbohydrate depletion in the subtending source leaf and the remainder of the plant. Collectively, the results indicated that under the conditions employed, leaves are the whole plant's primary source of carbon at night as well as during the day.     

Physiological integration in the clonal perennial herb Trifolium repens L.

Summary Translocation of ¹⁴C-labelled carbohydrates between the parent stolon and branches, and among branches, of Trifolium repens plants was investigated in two glasshouse experiments to determine patterns of physiological organisation in this clonal species. Differential defoliation treatments were applied to the parent stolon and/or branches to test the sensitivity of translocation to the short-term carbon needs of defoliated sinks. Strong reciprocal exchange of carbohydrate between the parent stolon and branches was observed, with 18 41% of the ¹⁴C exported from leaves on the parent stolon moving to branches, while branches simulta-neously exported 25% (for old source branches) to 54% (for young source branches) of the ¹⁴C they assimilated to the parent plant, including translocation to other branches. Branch-to-branch translocation occurred both acropetally and basipetally. Parent-to-branch, branch-to-parent and branch-to-branch carbon fluxes all increased in response to defoliation of the sink, at the expense of carbon supply to stolon tissue or roots of the source module. Reduced export to stolon tissue of the parent axis played a major role in facilitating C reallocation from leaves on the parent stolon to defoliated branches. The observed patterns of C allocation and translocation could be adequately explained by accepted source-sink theory, and are consistent with a high degree of intra-plant physiological integration in resource supply and utilisation. This information provides mechanistic explanations for aspects of the growth dynamics and ecological interactions of T. repens in the patchy environment of a grazed pasture.     

Effects of irradiation level on leaf growth of sunflower

Sunflower, Helianthus annuus L. cv. INRA 6501, plants were grown in a gravel culture subirrigated with Hoagland nutrient solution, at photosynthetically active radiation levels of 15, 30 and 60 W m^-2 at a daylength of 16 h, a temperature of 20°C and a relative humidity of 60% throughout. Development of the plant and growth of the leaves were measured. High irradiance accelerated development proportionally in all phases from germination, through leaf initiation, primordial flower formation and the maturation of all plant organs until anthesis. High irradiance levels stimulated the expansion of the growing shoot, which produced more and larger primordia. Under constant conditions the ratio between leaf initiation rate and mature length of a leaf remained constant, although the growth patterns [relationship between relative growth rate (RGR) and organ age] of successive leaves were not similar. Consequently, it may be assumed that, as in poplar, the increasing size of the growing shoot reflects the increase of the vascular system of sunflower. The growth patterns of the leaves depend on the developmental stage of the plant and, in the young primordial stage, also on irradiance level. In the linear phase of growth the growth pattern is independent of irradiance level.