An Analysis of the Influence of Plant Density on the Growth of Vicia faba: I. THE INFLUENCE OF DENSITY ON THE PATTERN OF DEVELOPMENT

The competitive effects of varying the density on the developmentof Vicia faba have been studied in a series of multifactorialexperiments where the spacing both between and within rows wassimultaneously altered. Over densities ranging from 11 to 67plants per metre² seed production on an area basis tended tobe maximal at 35–45 plants per metre² in the winter typeand at the highest density for the spring type. As the densityincreased the number of pods per plant and the extent of branchingfell progressively but there was no appreciable change in eitherseed size or the number of seeds per pod: thus seed productionwas solely governed by the number of mature pods formed. Thenumber of flowers per plant was more dependent on the numberof inflorescences than on the number of flowers per inflorescence.Increasing the population diminished the number of nodes bearinginflorescences particularly in the upper part of the shoot,while the size of the inflorescence was decreased to a lesserextent. The number of flowers forming mature pods was very small(9–14 per cent.). At the top of the shoot the flowerswere infertile, while above the middle node most of the podsformed were shed while still immature. Thus the primary effectof increasing density was to depress the number of nodes onthe lower half of the stems which produced mature pods. By thetime the flowering stage was reached plant height was alreadycorrelated with density due more to a change in internode lengththan an alteration in the number of differentiated nodes; atmaturity the differences in height were smaller due to the greaternumber of nodes in the widely spaced plants. For a given density,alterations in the distance between rows had little influenceon development. The possible physiological factors responsiblefor the changing pattern of development brought about by varyingdensity are discussed.     

Auxins,ABA and gibberellin-like activity in abscising and non-abscising flowers and pods of Vicia faba L.

Abscission probability varies among floral positions within inflorescences of Vicia faba L. Flowers from proximal positions have a greater chance to develop into mature pods than flowers from more distal positions which normally abscise either as older flowers or as young pods. In three field experiments with the indeterminate single stem variety Herz-Freya, changes in the contents of extractable auxins, abscisic acid (ABA) and gibberellins in flowers and pods during their development, and their possible influence on abscission were investigated.Inflorescences at different positions along the stem were divided into the two proximal and the remaining fruits. The content of all three hormones was at a low level during flower development, increased greatly in parallel with dry matter accumulation in the young pods, and then decreased to maturity. The first hormone to increase in the fruits was auxin and this took place when abscission from the distal positions began. ABA and gibberellins at this time were still at a low level. This ontogenic course of hormone production was very similar in fruits of both positions within an inflorescence, but in flowers and young pods from proximal positions, auxin content in most inflorescences was greater than in those from the abscising distal positions. No such positional differences were observed with ABA and gibberellins. Decapitation of the plants reduced flower and pod drop from the remaining reproductive nodes. Although decapitation resulted in less abscission among distal flowers and young pods from these nodes, it did not affect the ontogenic course of auxin and ABA production in these fruits.     

Factors affecting the Abscission of Reproductive Organs in Yellow Lupins (Lupinus luteus L.): I. THE EFFECT OF DIFFERENT PATTERNS OF FLOWER REMOVAL

1. The effect of various patterns of flower removal on pod settingwas investigated in Lupinus luteus L. Four-fifths, three-fifths,or two-fifths of the flowers of the main inflorescence wereremoved according to ten different patterns. 2. All flowers could produce pods but later ones were less efficientin doing so. Developing pods had an abscission-inducing effecton later flowers, which became increasingly effective towardsthe apical part of the inflorescence. More pods were retained when flowers on each consecutive whorlwere arranged in a spiral than when the same number was arrangedvertically. Pod setting was incomplete when the number of flowers per inflorescencewas reduced well below the total number of pods normally present. 3. The number of ovules in consecutive flowers gradually decreasedfrom an average of 5.7 at the base to 4.3 at the top of theinflorescence. The ratio of seeds to ovules fluctuated irregularlybetween 65 and 94 per cent, and did not indicate a general trendin embryo abortion. 4. The growth-rate of pods at the top of the inflorescence wasmuch slower than at the bottom. Vascular differentiation wasalmost absent at the top of the inflorescence when the flowerswere fertilized, and further vascular tissue was produced onlywhen flowers produced pods.     

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。     

Dry matter accumulation at specific pod positions on field bean (Vicia faba L.) plants and possible relations with indoleacetic acid and abscisic acid levels

Seed weights at specific positions within inflorescences of field bean plants (Vicia faba L.) were varied by removal of flowers. The inflorescences of two regions (nodes 3+4 and nodes 5+6, counted from the bottom of the plant) were used for manipulations and investigations. The two proximal flowers of the manipulated inflorescence were removed in order to vary the development and seed weights of distal pods (see Fig. 1). Dry matter accumulation and IAA- and ABA-concentrations in seeds were investigated during the filling period. Treatment effects in both regions were similar during two seasons. The removal of proximal flowers prevented the usually observed drop of distal pods and favoured the accumulation of dry matter and IAA in seeds, whereas the variation of ABA-concentrations partly depended on interaction with season. Whether these effects contribute to a signal leading to the establishment of processes preceeding dry matter accumulation or are a consequence of such processes is questionable.     

Density Studies on Lupins. II. Components of Seed Yield

Components of seed yield of cv. Ultra (Lupinus albus L.) andcv. Unicrop (L. angustifolius L.) were measured when grown atthree densities. The low density (10 plants m^–2) Unicropyield (34 g seed per plant) was 1.8 times that of Ultra as ithad more branches, pods and seeds per pod. Ultra seeds (310mg per seed) were heavier than Unicrop seeds (180 mg). The branchingpattern of Ultra was less dependent on plant density, henceat 93 plants m^–2 it gave a higher per plant yield (7.4vs 6.4 g) than Unicrop at lower densities (83 plants m^–2).Density had most influence on pod formation and only small effectson seeds per pod and seed weight. Yield components on the main-steminflorescence were influenced less by density than componentson branch inflorescences. Later formed, higher order generationsof inflorescences were most affected by increased inter- andintra-plant competition. Pod numbers on the main-stem were similarfor both species. Pods formed at higher flower nodes in Unicrop,but the lower flower nodes were less fertile than those in Ultra.Node position of flowers had no influence on seed set in main-stemUnicrop pods, but pods from higher nodes in Ultra formed fewerseeds. Seed weights in Unicrop were similar among main-stemnodes but in Ultra seed weights tended to increase at highernodes. Lupinus spp, lupins, seed yield, planting density     

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.     

DEMOGRAPHIC ASPECTS OF FLOWER AND FRUIT PRODUCTION IN BEAN PLANTS,PHASEOLUS VULGARIS L.

In this paper we assess the relative contributions to total pod yield of cohorts of flowers of known age. Bean plant (Phaseolus vulgaris L.) growth was monitored and 'births' of individual flowers were recorded and their fates followed. For every cohort of flowers an array of yield measures was calculated, including the mean and total cohort dry weight of fruits, and the numbers of viable and aborted seeds and completely undeveloped ovules. When mature, pods were removed from half of the plants. Plants whose mature pods were removed produced significantly greater numbers of flowers, ovules and viable seeds and a greater total weight of pods than did untreated plants. However, the proportion of ovules giving rise to viable seeds and to aborted seeds and undeveloped ovules was the same in plants of both groups. Approximately 50% of ovules of marketable pods, in all plants, yielded viable seeds. The 12 cohorts of flowers contributed markedly different amounts to plant yield. Early and later cohorts contributed much less than did middle cohorts in terms of marketable pod dry weight and numbers of fully developed seeds, aborted seeds, and undeveloped ovules. Peak productivity was therefore obtained from the middle phase of flowering in these annual bean plants. The lower pod yield of later cohorts is interpreted as a result of competition for limited resources between maturing pods and new flowers. We consider possible causes for the various fates of flowers and ovules and discuss flowers as plant modules suitable for demographic examination.     

Effetto della rimozione dei fiori sulla crescita delle piante e sul contenuto in leghemoglobina dei tubercoli radicali di pisello e fava

Abstract

Observations on vegetative growth and leghemoglobin contents of root nodules of pea and bean plants after flower bud removal. — These studies found their origin in the papers by MATTIROLO (1899) on the effect of the removal of flowers as they formed in bean plants; he observed that deflowering resulted in extraordinary plant growth, stem branching and flower buds formation as well as in a delayed root nodule senescence. In the light of modern knowledge of the leghemoglobin role in symbiotic nitrogen fixation, the aim of the present research was to ascertain any possible relation between flower bud removal and haeme pigment contents in the root nodules. The experiments were carried out during two growing seasons (1966 and 1970) using Vicia faba L. cv. Regina and Pisum sativum L. cv. Senatore during 1966 and cv. Vittoria in 1970. In both control and test plants the seasonal trends of average plant height, fresh and dry weight of vegetative portions, fresh and dry weight of root system, fresh weight of nodules, root nodule leghemoglobin concentration and total leghemoglobin content per plant, were determined. The data obtained are quoted in Table 2 and reported in Figures 1, 2, and 3. The removal of flower buds caused in both species: an increased plant growth, a marked stem branching, a longer blooming period, an increased flower number, an increased root nodule number and a certain delay in root nodule reabsorption. Deflowering did not significantly extend — at least in the species studied — life span (senescence was delayed only of one week). On the basis of these and of other Authors' results, we conclude that deflowering may actually delay senescence; the size of this delay, however, depends on the plant species considered and is fairly negligible both in pea and bean. The different effects of deflowering and of preventing floral induction on life span extension, are discussed, and these facts lead to consider floral induction as the onset of a chain of processes leading annual plants toward senescence in a more or less delayable, but definitive way. After having stressed the generally accepted importance of leghemoglobin concentration as an index of nodule nitrogen fixing ability, a correlation between biomass increase of test plants and number and total weight increase of root nodules, is put in evidence. No correlation between test plant biomass and the leghemoglobin concentration in root nodules, was however observed. Leghemoglobin concentration in root nodules is known to change in connection with various factors depending either on host plants and on Rhizobium strains and also in connection with several environmental conditions. Any prevented flower onset (ROPONEN and VIRTANEN, 1968) and deflowering (our data) however exerted no significant influence. The effects of flower bud removal were therefore the following: increased stem, leaf and root weights and increased root nodule number; no difference between control and test plants was however observed as regards size and leghemoglobin concentration of root nodules and hence probably no difference as regards their nitrogen fixing ability.     

Comparisons of Earlier- and Later-formed Pods of Chickpeas (Cicer arietinum L.)

In chickpeas (Cicer arietinum L.) flowering and pod developmentproceed acropetally. In plants grown under normal field conditionsat Hyderabad, in peninsular India, and at Hissar in north India,at successively apical nodes of the branches there was a declinein pod number per node, weight per pod, seed number per podand/or weight per seed. The percentage of nitrogen in the seedswas the same in earlier and later-formed pods at Hyderabad;at Hissar the later-formed seeds contained a higher percentage.Earlier- and later-formed flowers contained similar numbersof ovules. The decline in seed number and/or weight per seedin the later-formed pods of 28 out of 29 cultivars indicatedthat pod-filling was limited by the supply of assimilates orother nutrients. By contrast, in one exceptionally small-seededcultivar there was no decline in the number or weight of seedsin later-formed pods, indicating that yield was limited by ‘sink’size. Cicer arietinum L., chickpea, flowering, pod development, seed number, seed weight, nitrogen content     

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.

     

An Analysis of the Influence of Plant Density on the Growth of Vicia faba: II. THE SIGNIFICANCE OF COMPETITION FOR LIGHT IN RELATION TO PLANT DEVELOPMENT AT DIFFERENT DENSITIES

In a further analysis of the changing pattern of developmentinduced in Vicia faba by varying the density, it has been foundthat a reduction from a high to a low density has little influenceon the subsequent development unless such thinning is delayeduntil the flowering phase. By this time, save for widely spacedplants, the level of self shading within the population hasbecome marked. In fact, at high densities (55–65 plants/metre²)during the early-ripening phase the light intensity at groundlevel may fall to 0.03 daylight while a considerable proportionof the plant—up to 38 per cent.—may receive lessthan o-1 daylight. At low densities (11-I2 plants/metre²) theminimum intensity at ground level is 0.14 daylight and lessthan 3 per cent, of the shoot is subjected to o-1 daylight.In pot experiments, using a range of screens, it was establishedthat the compensation point is about o-I daylight. Thus, asthe density is increased the light gradient between the apexand the base becomes progressively steeper and the proportionof the leaves not actively assimilating correspondingly greater. To assess the ways in which such a light gradient operates,experiments were carried out in which either the apex or theinflorescences or leaves were removed over different sectionsof the stem or various parts of the shoot shaded and detailedrecords made of development, particularly of flower- and pod-production.Removal of the upper leaves or shading the apex primarily increasesthe rate of pod abscission after the flowers have set. Partialremoval of the inflorescences, especially at the lower nodes,has an opposite effect, while decapitation, though it augmentsthe percentage of flowers which produce immature pods, subsequentlycauses fewer pods to reach maturity. Shading of the lower nodesreduces at these nodes the number of mature pods but may resultin more pods maturing at the upper nodes. It is concluded that when the light gradient is such as to restrictthe internal supplies of substrates the growth of those organswith the least competitive ability, e.g. the newly formed pods,is arrested. It is at this phase that the factors controllingabscission come into play and that abscission is dependent upona balance between the levels of auxins and the production ofan abscission factor.     

Comparisons of Earlier- and Later-formed Pods of Pigeonpeas (Cajanus cajan (L.) Millsp.)

On branches of indeterminate cultivars of pigeonpea, floweringbegins at the basal nodes and proceeds acropetally; in morphologicallydeterminate cultivars, flowering begins on the apical racemesand proceeds basipetally. In cultivars of both types, withinthe racemes flowering proceeds acropetally. Under normal conditionsmore pods are set from earlier-formed flowers than from later-formedflowers, many of which are shed. Consequently the earlier-formedpods are found at the more basal nodes of racemes, and in indeterminatecultivars at the more basal nodes on the branches. The averageweight of earlier and later-formed pods, collected from thebasal and apical nodes of the racemes or of the branches, wassimilar; so was the number of seeds per pod, the weight perseed and the nitrogen content of the seeds. This pattern differsfrom that found in most herbaceous legumes, where later-formedpods are smaller, and indicates that pigeonpeas set fewer podsthan they are capable of filling. This behaviour may be relatedto the intrinsically perennial nature of pigeonpeas. The comparisonof the weights of earlier- and later-formed pods could providea simple screening procedure for identifying plants with anannual nature among existing cultivars or in breeders' lines. Cajanus cajan (L.) Millsp., pigeonpea, pod development, seed number, seed weight, nitrogen content     

Effects of Botrytis fabae infection and mechanical defoliation on seed yield of field beans (Vicia faba)

Effects on seed yield of mechanical defoliation and inoculation with Botrytis fabae were compared using pot-grown plants of Vicia faba (cv. Maris Beagle). Treatments, which were made at the end of flowering, were applied singly and in all combinations to leaves (a) below, (b) at, and (c) above the flowering nodes (i.e. 2³ factorial). Yield was unaffected by treatments applied to leaves below the flowering nodes. Removal of leaves at flowering nodes did not reduce the number of pods but yield was reduced because there were fewer and smaller seeds. Inoculation of this zone also reduced yield; pods were lost at some nodes but it could also be shown that, irrespective of pod loss, yield at individual nodes was reduced in proportion to the severity of infection on leaves at the same nodes. Removal of leaves above flowering nodes reduced yield almost to the same extent as removal of leaves at flowering nodes but inoculation resulted in only a small amount of infection and yield was not reduced significantly. These results, taken in conjunction with recent studies on the physiology of the host plant, show that beans are exceptionally vulnerable to attack by B. fabae at the stage of flowering and early pod development. At later stages of development infection is unlikely to have a substantial effect on yield.     

Sink removal and leaf senescence in soybean : cultivar effects

Three cultivars of soybean (Glycine max [L.] Merr. cvs Harper, McCall, and Maple Amber) were grown in the field and kept continuously deflowered throughout the normal seedfill period. For all cultivars, deflowering led to delayed leaf abscission and a slower rate of chlorophyll loss. Compared to control plants, photosynthesis and ribulose 1,5-bis-phosphate carboxylase/oxygenase (Rubisco) level declined slightly faster for deflowered Harper, but for both McCall and Maple Amber, leaves of deflowered plants maintained approximately 20% of maximum photosynthesis and Rubisco level 1 month after control plants had senesced. Deflowering led to decreased leaf N remobilization and increased starch accumulation for all cultivars, but cultivars differed in that for McCall and Maple Amber, N and starch concentrations slowly but steadily declined over time whereas for Harper, N and starch concentrations remained essentially constant over time. SDS-PAGE of leaf proteins indicated that for all cultivars, deflowering led to accumulation of four polypeptides (80, 54, 29, and 27 kilodaltons). Western analysis using antisera prepared against the 29 and 27 kilodalton polypeptides verified that these polypeptides were the glycoproteins previously reported to accumulate in vacuoles of paraveinal mesophyll cells of depodded soybean plants. The results indicated that depending on the cultivar, sink removal can lead to either slightly faster or markedly slower loss of photosynthesis and Rubisco. This difference, however, was not associated with the ability to synthesize leaf storage proteins. For any particular cultivar, declines in chlorophyll, photosynthesis, and Rubisco were initiated at approximately the same time for control and deflowered plants. Thus, even though cultivars differed in rate of decay of photosynthetic rate and Rubisco level in response to sink removal, the initiation of leaf senescence was not influenced by presence or absence of developing fruits.     

Injury to oilseed rape caused by mirid bugs (Lygus) (Heteroptera: Miridae) and its effect on seed production

Injury by Lygus spp. to oilseed rape, Brassica napus L. and Brassica campestris L., was assessed based on laboratory and field studies in Alberta, Canada. The visible injuries consisted of lesions on the surfaces of stems, buds, flowers and pods similar to those described for other crops. They caused buds and flowers to abscise and seeds to collapse, and reduced the weight of healthy seeds produced per pod. The plants compensated for bud loss so that no net reduction in the number of pods occurred. However, in some situations the damage to buds resulted in a reduced seed yield that increased with the amount of injury. The plants also compensated for flower loss so that no net reduction in the number of pods occurred, but seed yield declined as injury increased. Plants did not compensate for seeds that collapsed as a result of lygus feeding. The feeding activity of lygus bugs reduced seed yield in oilseed rape.     

Effect of ascochyta blight (Mycosphaerella pinodes) on yield components of single pea (Pisum sativum) plants under field conditions

Field studies were made in 1992 and 1993 to examine the yield components of pea inoculated with Mycosphaerella pinodes and those of healthy pea (sprayed with a mixture of flutriafol + chlorothalonil), in a split-plot design with the cv. Solara sown at different plant densities. Ascochyta blight was severe on leaves and on internodes of the basal part of the plants; pods had few lesions. The number and length of stems per plant were the same for diseased and healthy plants. The number of reproductive nodes and pods per stem were affected by disease only in 1993. In 1992 and 1993 respectively, disease caused reductions in the number of seeds per stem of 18% and 25%, and in seed size of 13.5% and 16.7%, compared with healthy plants. The harvest index and total biomass were lower in diseased than in healthy plants and seed yield was reduced by 40% in diseased plots. These results show a high relationship between the disease parameters (disease mean on stipules/nodes 8–18/ and on internodes/nodes 5–15/, percentages of stipules or internodes with a disease score 4, and percentage of stems encircled by lesions), plant density and yield reduction.     

The Influence of Genes ar and n on Senescence in Pisum sativum L.

The effect of genes ar (violet flowers, small hilum) and n (thick,fleshy pod wall) on whole plant in senescence peas was examinedby comparing Ar- with arar and N- with nn plants in segregatingprogenies. Homozygosity for ar or n significantly delayed the time whenthe plants were ready for harvest of their entire seed crop.These genes did not delay either the onset of reproduction orthe onset of apical arrest in the first instance. However, whereasAr- N- plants almost invariably senesced and died as the firstseed crop matured, the majority of arar and/or nn plants entereda period of secondary growth and a further fruiting cycle. Comparedwith Ar- plants, arar plants had over twice as many pods andseeds but individual seeds were 58 per cent lighter and totalseed yield (wt) was 19 per cent less. Pod length was unaffected.Compared with N-plants, nn plants had shorter pods (16 per cent),fewer seeds per pod (21 per cent), smaller seeds (20 per cent)and a lower total seed yield (wt 14 per cent less). It appearsthat ar and n impose a lower metabolic drain per reproductivenode as a consequence of their effects on hilum anatomy andpod morphology, respectively. These mutants disrupt the normalpattern of monocarpic senescence by breaking the coordinationbetween apical arrest and subsequent events. The developingseed crop delimited by the first arrest fails to cause plantdeath, possibly because sink size is less than in normal counterparts. Pisum sativum L, garden pea, senescence, hilum, pod, seed size, genetics     

Yield components and cultivar, sowing date and density in field beans (Viciafaba)

Delay in sowing the cultivars Ostlers (Viciafaba var. equina) and Herz Freya (V.faba var. minor) beyond late February depressed yield. Densities of at least sixty plants per m² were required to ensure that yield was not limited by sowing rate. Differences in yield in response to changes in density were reflected particularly in changes in numbers of pod-bearing nodes per plant, but also to a lesser extent in numbers of pods per pod-bearing node. The inherently larger seed weight of cv. Ostlers compared with cv. Herz Freya did not confer any yield advantage, differences in number of beans per pod and number of pods per pod-bearing node tending to equalize the yield of the two cultivars. The most stable component of yield throughout was number of beans per pod, and the least stable was number of pod-bearing nodes per plant.     

Synthesis and degradation of a 28-kDa pod storage protein in French bean (Phaseolus vulgaris) plants

Pod storage protein (PSP) accumulated in developing pods of French bean (Phaseolus vulgaris L.) plants, and increasing the PSP mRNA level by pod removal resulted in the enhancement of PSP accumulation in pods that formed later. Pod storage protein was detected in flowers, young leaves and young stem internodes in addition to pods. Accumulation of PSP and its mRNA was induced by sink-removal in an organ-specific manner. In addition, wounding induced PSP accumulation systemically in leaves. Methyl jasmonate did not induce PSP synthesis but enhanced the synthesis that was induced by wounding. In senescing pods, PSP was degraded, and degradation products with molecular masses of 20 and 17 kDa were detected in the pods. The amount of 20-kDa degradation product was greater than that of the 17 kDa product. Received: 26 May 1999 / Accepted: 24 June 1999