Light and Shade Effects on Abscission and C-Photoassimilate Partitioning among Reproductive Structures in Soybean

Field experiments were conducted in 1981 and 1982 to study the effects of low-irradiance supplemental light on soybean (Glycine max [L.] Merr. cv Evans) flower and pod abscission. Cool-white and red fluorescent lights illuminated the lower part of the soybean canopy during daylight hours for 3 weeks late in flowering. At the same time, flowers and young pods on half the plants were shaded with aluminum foil. Flowers were tagged at anthesis and monitored through abscission or pod maturity.

Responses to red and white lights were similar. Supplemental light tended to reduce abscission and increase seed weight per node compared to natural light. Shading flowers and pods increased abscission and reduced seed weight per node. Number of flowers produced per node, individual seed weight, and seeds per pod were not affected by light or shade treatments.

Further studies examined the effects of shading reproductive structures on their capacity to accumulate ¹⁴C-photoassimilates. Individual leaves were pulse labeled with ¹⁴CO₂ 1, 2, and 4 weeks post anthesis. Flowers and pods in the axil of the labeled leaf were covered with aluminum foil 0, 24, 72, and 120 hours before pulsing.

Shading flowers and pods resulted in a 30% reduction in the relative amount of radiolabel accumulated from the source leaf. The reduction in ¹⁴C accumulation due to shading was evident regardless of the length of the shading period and was most pronounced when the shades were applied early in reproductive development. We conclude that light perceived by soybean flowers and young pods has a role in regulating both their abscission and their capacity to accumulate photoassimilates.

     

Influence of assimilate demand on photosynthesis, diffusive resistances, translocation, and carbohydrate levels of soybean leaves

Rates of net photosynthesis and translocation, CO₂ diffusive resistances, levels of carbohydrates, total protein, chlorophyll, and inorganic phosphate, and ribulose 1,5-diphosphate carboxylase activity were measured in soybean (Glycine max L. Merrill) leaves to ascertain the effect of altered assimilate demand. To increase assimilate demand, the pods, stems, and all but one leaf (the “source leaf”) of potted plants were completely shaded for 6 or 8 days and the responses of the illuminated source leaf were monitored. Rate of net photosynthesis in the source leaf of the shaded plants was found to increase curvilinearly to a maximum on the 8th day. The source leaf of the control plants (no sink shading) maintained a constant photosynthetic rate during this period. Vapor-phase resistance to CO₂ diffusion did not vary with treatment, but mesophyll (liquid phase) resistance was significantly lower in the source leaf of the shaded plants.     

Records of Source--Sink Relations by Means of Respiration Measurements

A method for recording respiration rates of attached singlesoybean pods is described. By means of such records source-sinkrelations can be observed over an extended period of time ifphotosynthesis of leaves is recorded simultaneously. It is shownthat there are direct influences on respiration, such as changesin temperature and indirect effects which influence primarilythe assimilate influx into the pods, e.g. light and competitionbetween pods. The shading of a single leaf next to the pod has only a smalleffect because the pod is supplied by more than one leaf. Bygirdling the plants, the export-import conditions can be studiedon a single leaf as source and a single pod as sink. The resultsshow that a trifoliate fully-grown leaf produces more assimilatethan can be used by a single pod. If only one pod is growingwithin the girdled area then starch is accumulated and the photosyntheticrate of the leaf is greatly reduced. The respiration rate ofthe pod is only slightly increased, in spite of the abundantavailability of assimilates. It appears therefore, that thefilling rate of pods is determined mainly by the capacity ofthe pod to off-load the phloem, and cannot be increased beyonda certain level by additional sucrose influx. Our results show that, using this method, the source-sink relationscan be recorded qualitatively over time periods of 3–4weeks. Key words: Source-sink relations, pod respiration, Glycine max, pod filling, photosynthesis     

外源乙烯利施用时期对花生源库形成的调控效应

为了解决源库关系不协调而限制花生产量提高的问题,在大田栽培条件下,以‘山花9号’花生为试验材料,设置花后10、20、30 d 3个喷施时期,以不喷施处理为对照,探讨不同时期喷施乙烯利对花生源库形成的调控效应。结果表明: 花后10和20 d喷施乙烯利可显著减少花生的开花数量、果针数、幼果数,提高秕果数和饱果数,而花后30 d喷施处理对开花数量、果针数和幼果数无抑制作用。喷施乙烯利可以增加花生单株叶面积,开花后10 d喷施处理的单株叶面积增幅最大,随着喷施时期的推迟增幅减小。花后10和20 d喷施乙烯利显著提高了花生叶片的光合速率,但花后30 d喷施处理只能在短期内提高光合速率,对生育后期的叶片光合速率无显著影响。从源库综合性状来看,花后20 d喷施乙烯利的源库关系最协调,有利于促进同化物向荚果的运输,提高有效果比例和荚果充实度,从而提高产量。因此,喷施乙烯利是解决花生“花多不实、果多不饱”源库失衡现象的有效措施,生产中使用乙烯利控花应选择在开花后20 d喷施。     

Changes in photosynthetic rates and gene expression of leaves during a source-sink perturbation in sugarcane

BACKGROUND AND AIMS: In crops other than sugarcane there is good evidence that the size and activity of carbon sinks influence source activity via sugar-related regulation of the enzymes of photosynthesis, an effect that is partly mediated through coarse regulation of gene expression. METHODS: In the current study, leaf shading treatments were used to perturb the source-sink balance in 12-month-old Saccharum spp. hybrid 'N19' (N19) by restricting source activity to a single mature leaf. Changes in leaf photosynthetic gas exchange variables and leaf and culm sugar concentrations were subsequently measured over a 14 d period. In addition, the changes in leaf gene response to the source-sink perturbation were measured by reverse northern hybridization analysis of an array of 128 expressed sequence tags (ESTs) related to photosynthetic and carbohydrate metabolism. KEY RESULTS: Sucrose concentrations in immature culm tissue declined significantly over the duration of the shading treatment, while a 57 and 88% increase in the assimilation rate (A) and electron transport rate (ETR), respectively, was observed in the source leaf. Several genes (27) in the leaf displayed a >2-fold change in expression level, including the upregulation of several genes associated with C(4) photosynthesis, mitochondrial metabolism and sugar transport. Changes in gene expression levels of several genes, including Rubisco (EC 4.1.1.39) and hexokinase (HXK; EC 2.7.1.1), correlated with changes in photosynthesis and tissue sugar concentrations that occurred subsequent to the source-sink perturbation. CONCLUSIONS: These results are consistent with the notion that sink demand may limit source activity through a kinase-mediated sugar signalling mechanism that correlates to a decrease in source hexose concentrations, which, in turn, correlate with increased expression of genes involved in photosynthesis and metabolite transport. The signal feedback system reporting sink sufficiency and regulating source activity may be a potentially valuable target for future genetic manipulation to increase sugarcane sucrose yield.     

Characterization of leaf senescence and pod development in soybean explants

Excised soybean (Glycine max [L.] Merrill) cv Anoka leaf discs tend to remain green even after the corresponding intact leaves have turned yello on fruiting plants. We have found that explants which include a leaf along with a stem segment (below the node) and one or more pods (maintained on distilled H₂O) show similar but accelerated leaf yellowing and abscission compared with intact plants. In podded explants excised at pre-podfill, the leaves begin to yellow after 16 days, whereas those excised at late podfill begin to yellow after only 6 days. Although stomatal resistances remain low during the first light period after excision, they subsequently increase to levels above those in leaves of intact plants. Explants taken at mid to late podfill with one or more pods per node behave like intact plants in that pod load does not affect the time lag to leaf yellowing. Explant leaf yellowing and abscission are delayed by removal of the pods or seeds or by incubation in complete mineral nutrient solution or in 4.6 micromolar zeatin. Like chorophyll breakdown, protein loss is accelerated in the explants, but minerals or especially zeatin can retard the loss. Pods on explants show rates and patterns of color change (green to yellow to brown) similar to those of pods on intact plants. These changes start earlier in explants on water than in intact plants, but they can be delayed by adding zeatin. Seed dry weight increased in explants, almost as much as in intact plants. Explants appear to be good analogs of the corresponding parts of the intact plant, and they should prove useful for analyzing pod development and mechanisms of foliar senescence. Moreover, our data suggest that the flux of minerals and cytokinin from the roots could influence foliar senescence in soybeans, but increased stomatal resistance does not seem to cause foliar senescence.     

Carbon Partitioning and Growth of a Starchless Mutant of Nicotiana sylvestris

We have further characterized the photosynthetic carbohydrate metabolism and growth of a starchless mutant (NS 458) of Nicotiana sylvestris that is deficient in plastid phosphoglucomutase (Hanson KR, McHale NA [1988] Plant Physiol 88: 838-844). In general, the mutant had only slightly lower rates of photosynthesis under ambient conditions than the wild type. However, accumulation of soluble sugars (primarily hexose sugars) in source leaves of the mutant compensated for only about half of the carbon stored as starch in the wild type. Therefore, the export rate was slightly higher in the mutant relative to the wild type. Starch in the wild type and soluble sugars in the mutant were used to support plant growth at night. Growth of the mutant was progressively restricted, relative to wild type, when plants were grown under shortened photoperiods. When grown under short days, leaf expansion of the mutant was greater during the day, but was restricted at night relative to wild-type leaves, which expanded primarily at night. We postulate that restricted growth of the mutant on short days is the result of several factors, including slightly lower net photosynthesis and inability to synthesize starch in both source and sink tissues for use at night. In short-term experiments, increased “sink demand” on a source leaf (by shading all other source leaves) had no immediate effect on starch accumulation during the photoperiod in the wild type or on soluble sugar accumulation in the mutant. These results would be consistent with a transport limitation in N. sylvestris such that not all of the additional carbon flux into sucrose in the mutant can be exported from the leaf. Consequently, the mutant accumulates hexose sugars during the photoperiod, apparently as the result of sucrose hydrolysis within the vacuole by acid invertase.     

Alteration of C-assimilate partitioning in leaves of soybeans having increased reproductive loads at one node

The objectives of this study were to determine if the partitioning of recently fixed carbon between starch and water-soluble compounds could be altered by increasing the pod load in the leaf axil, and if the presence of source leaves acropetal to such a node would influence the partitioning of carbon within the subtending leaf. Soybeans (Glycine max L. Merr. cv Hodgson 78) were grown to full-bloom in a controlled environment chamber, and then deflowered at all nodes except the eighth. This treatment resulted in an 83% increase in the number of pods at the eighth node. At 24 days after flowering, one-half of the treated plants were girdled above the untreated node. Forty-two hours later, the eighth trifoliolate was pulsed with ¹⁴CO₂ and sampled for radiolabeled starch and water-soluble compounds (WSC) at 0.5, 2, 4, 8, 12, and 24th after labeling.

When no girdling was applied above the increased pod load at the eighth node more label was accumulated by the pod walls (+6.9%) and seeds (+6.3%) when compared to the controls. Starch accumulation was not altered in the labeled leaf of the nongirdled plants. When the stem was girdled above the eighth node, significantly less starch was retained in the labeled leaf. Girdling also resulted in an increase in label accumulation by the pod walls (+5.4%) and seeds (+6.6%). These data suggest that the plant will change the distribution patterns of assimilate to supply added sink demand before altering the partitioning of recently fixed carbon in the subtending leaf.

     

The Control of the Light Acclimation of Photosynthesis in Glycine max: Dependence on Import as Modified by Intraplant Shading

The dependence of photosynthetic capacity on imported and locally-assimilatedsupplies of carbon during leaf development under different irradianceswas investigated in Glycine max. The potential export of carbonto the developing, mainstem trifoliate leaf (source-potential)was restricted non-destructively by shading all lower, sourceleaves (source-shading), while local photosynthesis was modifiedconcurrently by exposing the young leaf to different light levelsduring development. When source-shading was applied below the2nd mainstem trifoliate leaf at the bud stage of development,photosynthetic capacity was unaffected in leaves which had developedunder moderate and low irradiances (500 and 250 µmol PARm ^–2 s^–1 respectively), but was reduced significantlyin leaves developed under a high irradiance (900 µmolPAR m ^–2 s^–1). If source-shading was applied beneaththe 2nd leaf at unfolding, the reduction of photosynthetic capacityunder the high irradiance was relatively minor. The photosyntheticcapacity attained by the 2nd leaf during development under differentirradiances was influenced by the previous light environmentof the whole plant. In contrast to the 2nd leaf, the photosyntheticcapacities of the 1st and 4th mainstem leaves were relativelyunaffected by source-shading, even under the highest light regime.While photosynthetic capacity showed a widespread insensitivityto the light level of the lower region of the canopy, source-shadingreduced final leaf size irrespective of node position or localirradiance during leaf development. These effects were not relatedto differences in daily photosynthesis by the expanding leaf,and are discussed in terms of the source/sink balance of thedeveloping leaf. Key words: Glycine max, source-shading, photosynthetic capacity     

Alterations in source-sink patterns by modifications of source strength

Bean plants, trimmed to a simplified “double source, double sink” translocation system (the paired primary leaves serving as the double source and the paired lateral leaflets of the immature first trifoliate leaf as the double sink) were used to study the magnitude and short-term time course of change in the allocation ratio (partition ratio) of assimilates translocated from the labeled primary leaf to its respective “near” and “far leaflet” sinks in response to an increase or decrease in the source strength of the opposite primary leaf (the “control” leaf). If the rates of net photosynthesis in the two primary leaves were similar, assimilates from the labeled source leaf partitioned to the leaflet sinks in the ratio of 5:1 or higher, the dominant sink being the leaflet “nearer” to the labeled source leaf. If the rate of net photosynthesis in the control leaf was increased substantially above that of the labeled source leaf, the rate of translocation from the labeled source to either the near leaflet sink or far leaflet sink remained unaffected, despite, presumably, a higher translocation rate from the control leaf, and hence a higher phloem pressure gradient (or increased cross-sectional area) in the transport pathway from the control leaf to the leaflet sinks. If the control leaf was excised, thus reducing the source leaf area by about a half, the translocation rate from the remaining source leaf rapidly doubled, the partition ratio becoming equal to unity. If the control leaf was darkened, the partition ratio adjusted to an intermediate value. Although export rates from the labeled source leaf were increased either by excising or darkening the control leaf, the rate of net photosynthesis in the labeled leaf remained constant.     

In field-grown coffee trees source-sink manipulation alters photosynthetic rates, independently of carbon metabolism, via alterations in stomatal function

Perturbations of the source-sink balances were performed in field-grown coffee (Coffea arabica) trees to investigate the possible role of carbohydrates in feedback regulation of photosynthesis. Four treatments were applied at the whole-plant level: (i) complete defruiting and maintenance of the full leaf area, (ii) the half crop load and full leaf area, (iii) the full crop load and full leaf area and (iv) the full crop load and half leaf area. Sampling and measurements were performed twice during the phase of dry matter accumulation of fruits. Gas exchange, chlorophyll a fluorescence, carbon isotope labelling and steady-state metabolite measurements were assessed in source leaves. The average rate of net photosynthetic rate (A) and stomatal conductance (g(s)) were larger (> 50%), and carbon isotope composition ratio was lower, in trees with a full crop load and half leaf area than in defruited trees, with individuals of the other two treatments showing intermediate values. However, differences in A seem unlikely to have been caused either by photochemical impairments or a direct end-product-mediated feedback down-regulation of photosynthesis. It is proposed that the decreased A in defruited coffee trees was independent of carbon metabolism and was rather directly related to a lower CO(2) availability coupled to lower g(s).     

Regulation of monocarpic senescence of Brassica campestris by the developing pods

Senescence of Brassica campestris L. cv. B-9 was studied with regard to seed maturation and source-sink relationships. In normal control plants leaf senescence (as determined by the change in chlorophyll level) started and proceeded in a progressive manner from base to apex during the period of early pod setting. Complete yellowing of the leaves occurred well before the seed maturation and pod wall senescence. The pod wall always senesced before the attainment of final seed weight. In two different sets of acrocarpous plants containing 65 pods and 10 pods, respectively, leaf senescence was delayed during the pod filling period. It started non-sequentially after complete yellowing and senescence of the pod wall. The degree of leaf senescence at the post-pod filling stage was almost proportional to the number of pods present. When peduncles of the acrocarpous 10-podded plants were removed after the pod filling stage of the plant, leaf senescence was delayed compared to plants whose pedicels were removed, although the senescence pattern of the upper three leaves was nonsequential in both cases. Defruiting at an early stage of development delayed leaf senescence, although the pattern of such senescence remained unaltered (i.e. nonsequential). Defoliation hastened the seed-filling process and pod wall senescence. Plants containing fewer pods had higher average seed weight, although yield per plant was reduced.
These results suggest that the pod wall serves as a temporary as well as intermediary storage organ and that foliar senescence is not directly related to seed maturation. The possible cause of uncoupling between foliar senescence and seed development is discussed.     

遮光对蚕豆花荚形成和脱落的影响

本文旨在研究蚕豆开花前后不同时期光照强度对花荚形成和脱落的影响。产量补偿能力以及花荚形成和脱落的生理生态原因。蚕豆花前遮光,开花总数和结荚数降低,但花荚脱落率下降,粒重增加。花期和花后遮光,对开花总数没有明显影响,但花荚脱落严重,减产最多。任何时期遮光均使比叶重、遮光后期叶绿素含量、光合生产量、生殖器官干物质分配率,可溶性糖和含N量下降,但成熟期可溶性糖和含N量,营养元素吸收量不受影响。遮光导致花荚形 成和产量减少的主要原因是C／N比值下降,而不是改变营养元素的丰度所致。     

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.     

Changes in total nitrogen, soluble protein, and peroxidases in the expanding leaf zone of eastern cottonwood

Nitrogen content and soluble protein and anodal peroxidase banding in acrylamide gel changed with leaf and internode development in the expanding leaf zone of eastern cottonwood (Populus deltoides Bartr.). Nitrogen per unit leaf area was high near the apex and decreased to a constant value at the sixth node below it. Soluble protein banding was qualitatively similar for leaves and internodes in this zone, but anodal peroxidases differed between leaves and internodes. The major leaf peroxidase band was absent from the second leaf below the apex but present in the fourth and sixth leaves; its appearance and intensification seemed to parallel the development of photosynthetic activity. The major internode peroxidase band was present in the apex, second, fourth, and sixth internodes, and intensified during internodal development. It is suggested that these two “isoenzymes” may have different functions in vivo.     

The effects of developmental stage and source leaf position on integration and sectorial patterns of carbohydrate movement in an annual plant, Perilla frutescens (Lamiaceae)

A well-integrated plant shows extensive carbohydrate translocation through the plant body. Even in highly integrated plants, however, translocation patterns will be sectorial if vascular tissue restricts carbon movement to sectors along stems. Both integration and sectorial translocation patterns are sensitive to plant architecture and thus may change as a plant develops. These patterns should vary also with the position of the source leaf because leaves at each node are unique in age and vascular relationship to the rest of the plant. I measured the effects of developmental stage and location of the source leaf on integration and sectoriality in an annual plant, Perilla frutescens, by labeling plants with C at one of three leaves and four developmental stages. Stage and source leaf affected both integration and sectoriality. Most notably, integration declined and sectoriality increased during seed fill, when resource demand at each node was high. Furthermore, translocation was least extensive from the leaf supporting the largest number of seeds on its axillary branch. These results suggest that plants are not homogeneous collections of subunits; rather, the role of each leaf in a plant's carbon budget is a function of its age and location on the plant.     

Short-term control of root: shoot partitioning

We present data showing that the fraction of the available photosynthatepartitioned between the root and the shoot of a barley seedlingis affected by the supply of photosynthate from the source leaf:an increased fraction of the exported photosynthate goes tothe shoot when supply is reduced. Also, if the roots are cooleda short time before reducing the supply of photosynthate, thenthe effect of a reduced supply upon partitioning is reversedwith an increased fraction then going to the root. We concludethat the distribution of available photosynthate between competingsinks is influenced by source supply as well as sink function.The reported source-sink interactions are consistant with thepredictions of a recently pro posed model of source-sink interaction(Minchin et al., 1993). The concept of marginal partitioningis introduced to describe the distribution, between all of thesinks, of a small change in photosynthate supply. Key words: Carbohydrate partitioning, shoot : root ratio, source-sink interactions     

Short and Long Term Fluctuations of the Leaf Mass Per Area of Tomato Plants--Implications for Growth Models

The leaf mass per unit leaf area (LMA) is a key variable inmany growth models, since it is often used to predict leaf areaexpansion from leaf dry weight increase, orvice versa. Influencesof source-sink balance on leaf area, leaf dry weight, LMA, andleaf content in non-structural carbohydrates were investigatedin glasshouse tomato crops. The source-sink balance was manipulatedby artificial shading, CO₂enrichment or fruit removal usingdifferent tomato cultivars. Leaf area was hardly affected bycompetition for assimilates except under extreme conditions.In contrast, leaf dry weight, and consequently LMA, underwentlarge and rapid fluctuations in response to any factor thatchanged source and sink activities. A 60% reduction of photosyntheticallyactive radiation involved a 24% decrease in LMA after 10 d.Carbon dioxide enrichment and fruit removal induced about a45% and 15% increase in LMA, respectively, on plants with twofruiting trusses, but hardly affected LMA of producing plants.No significant cultivar effect could be identified. Changesin starch and soluble sugar content in leaves accounted foronly 29% of diurnal variations in LMA, suggesting regular fluctuationsof other components. We propose that structural LMA varies betweena maximum and a minimum value according to the ratio of assimilatesupply and demand during leaf development. Leaf area is independentof the supply of assimilates when the minimum structural LMAis realised. When the maximum structural LMA is attained, astorage pool of assimilates may accumulate in leaves duringperiods of high supply and low demand. We present a model includingthese hypotheses, which predicts structural and non-structuralLMA variations of plants with different source-sink ratios.Copyright1998 Annals of Botany Company Tomato,Lycopersicon esculentumMill., SLA, SLW, leaf growth, vegetative sink strength, assimilate competition, source-sink ratio, non-structural carbohydrate, models.     

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.     

A study of several factors affecting the distribution of phosphorus-32 from the leaves ofPisum sativum

Summary 1. Distribution patterns for the movement of solutes in the phloem from leaves of pea plants were found to be relatively specific. Phosphorus-32 applied to the leaf at the first bloom node moved predominantly (to the extent of 50 to 90 per cent) to the pod at that node. Distribution of the translocate from this leaf to pods at higher nodes was negligible.2. Translocation in the phloem of phosphorus-32 from lower leaf nodes (i.e. 5th or 7th) was predominately downward with little or no accumulation in the pods.3. The stage of development of the flower markedly affected the distribution pattern of phosphorus-32 supplied to the leaf at the same node. Essentially no activity moved into either the flower or the vegetative portions of the plant before anthesis and fertilization had occurred in that flower, as compared to the same plant parts in plants 4 to 6 days past anthesis. The young developing embryos of the pod appear to control the movement of phosphorus-32 from the adjacent leaf.4. When the metabolic activity of the pod on plants bearing one pod only was lowered by cooling (to 7°C), the movement of phosphorus-32 to this pod as well as to all other parts of the plant was markedly diminished. This inhibitory effect of the low pod temperature on translocation to the uncooled parts of the plant was negated by the presence of a second pod (uncooled) on the plant. Lowering the temperature of the first pod resulted in a substantial increase in the proportion of the P³²-labelled translocate moving to the second pod.Paper No. 556 from Department of Botany and Plant Pathology, Ohio State University, Columbus 10, Ohio.