The Effect of Temperature on the Production and Abscission of Flowers and Pods in Snap Bean (Phaseolus vulgaris L.)

The effect of temperature on production and abscission of flowerbuds, flowers and pods was studied in a determinate snap-beancultivar (cv. Tenderette). Under moderate temperature (e.g.27/17°C) the onset of pod development was associated withcessation of flower bud production and with enhanced abscissionof flower buds. Raising night temperature from 17°C to 27°Cstrongly reduced pod production, mature pod size and seeds perpod, while an increase in day temperature from 22°C to 32°Chad smaller and less consistent effects. Pod production underhigh night temperature was not constrained by flower productionsince 27°C at night promoted branching and flower bud appearance.Under 32/27°C day/night temperature the large reductionin pod set was due to enhanced abscission of flower buds, flowersand young pods ( 3 cm). Flowers had the highest relative abscissionfollowed by young pods and flower buds. Therefore, the onsetof anthesis and of pod development were the plant stages mostsensitive to night temperature. Pods larger than 3 cm did notabscise but usually aborted and shrivelled under high nighttemperature. The effects of 32/27°C were not due to transientwater stresses and were observed even under continuous irrigationand mist-spraying. High temperature, flower production, pod set, seed set, abscission, snap bean, Phaseolus vulgaris L, Tenderette     

The Effect of Temperature on the Production and Abscission of Flowers and Pods in Snap Bean (Phaseolus vulgaris L.)

The effect of temperature on production and abscission of flowerbuds, flowers and pods was studied in a determinate snap-beancultivar (cv. Tenderette). Under moderate temperature (e.g.27/17 °C) the onset of pod development was associated withcessation of flower bud production and with enhanced abscissionof flower buds. Raising night temperature from 17 °C to27 °C strongly reduced pod production, mature pod size andseeds per pod, while an increase in day temperature from 22°C to 32 °C had smaller and less consistent effects.Pod production under high night temperature was not constrainedby flower production since 27 °C at night promoted branchingand flower bud appearance. Under 32/27 °C day/night temperaturethe large reduction in pod set was due to enhanced abscissionof flower buds, flowers and young pods (< 3 cm). Flowershad the highest relative abscission followed by young pods andflower buds. Therefore, the onset of anthesis and of pod developmentwere the plant stages most sensitive to night temperature. Podslarger than 3 cm did not abscise but usually aborted and shrivelledunder high night temperature. The effects of 32/27 °C werenot due to transient water stresses and were observed even undercontinuous irrigation and mist-spraying. High temperature, flower production, pod set, seed set, abscission, snap bean, Phaseolus vulgaris L., cv. Tenderette     

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.

     

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。     

Transmission of the Monocarpic Senescence Signal via the Xylem in Soybean

During monocarpic senescence in soybean (Glycine max [L.] Merrill cv. Anoka) there is a remobilization of nitrogen from the leaves to the seeds, and it has been hypothesized that this loss of nitrogen from the leaves induces foliar yellowing. The phloem in a small segment of the petiole between the pods and the target leaf can be inactivated with a jet of steam. When a plant is depodded except for a single pod cluster in the center of the plant, the pod cluster induces yellowing of the nearest leaf even if the petiole contains a zone of dead phloem, whereas most of the rest of the plant remains green. The nitrogen content of these leaves with a dead phloem zone in their petioles does not decrease greatly, even though the leaves turn yellow. A similar treatment of a single leaf on a fully depodded plant (leaves stay green) does not cause that leaf to turn yellow. Since nutrients would have to be withdrawn from the leaves via the phloem, the pods do not induce yellowing by pulling nutrients out of the leaf and must be able to exert their influence via the xylem.     

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.     

Pathway and regulation of phosphate translocation to the pods of soybean explants

We investigated the degree to which developing fruit compete directly with leaves for mineral nutrients, e.g. phosphate coming up from the roots. When soybean ( Glycine max (L.) Merrill cv. Anoka) explants cut at mid-late podfill were given a 15-min pulse of ³²Pi via the cut stem and then transferred to distilled water, 75% of the ³²P accumulated in the leaves and 21% in stem and petiole during the first hour. The amount of ³²P entering the seeds was low (1%) initially, but thereafter increased to 30% in 48 h. An accumulation of ³²P in the seed coats preceded its entry into the embryos. Disruption (with hot steam) of the phloem between the leaf and the pods after pulse labelling indicated that more than 80% of the ³²Pi pulse moved to the leaf before redistribution to the pods. Increasing "sink" size by adjusting the pod load from 1 to 2–3 did not increase the ³²P accumulated by the pods proportionally. Conversely, excision of the seeds after pulse labelling did not prevent translocation of ³²P out of the leaves. These results suggest that the rate of transport of phosphate to the pods at mid-late podfill is controlled primarily by factors in the leaves. The results are consistent with the observation that the relative size of the sink (pod load) does not regulate leaf senescence.     

Carbon Transfer and Partitioning between Vegetative and Reproductive Organs in Pisum sativum L

Assimilate partitioning was studied in the common pea (Pisum sativum L.) by feeding ¹⁴CO₂ to whole plants and measuring radioactivity in different organs 48 hours after labeling. Two experimental protocols were used. For the first, one reproductive node was darkened with an aluminum foil, to prevent photosynthesis during labeling. The aim was to study assimilate translocation among nodes. The second was carried out to assess any priority among sinks. Whole plants were shaded, during labeling, to reduce carbon assimilation. Various developmental stages between the onset of flowering and the final stage in seed abortion of the last pod were chosen for labeling. When all photosynthetic structures at the first reproductive node were darkened at any stage of development after the formation of the first flower, the first pod was supplied with assimilates from other nodes. In contrast, later developed pods, when photosynthetic structures at their node were darkened, received assimilates from other nodes only when they were beyond their final stage in seed abortion. Reducing illumination to 30% did not change distribution of assimilated carbon between vegetative and reproductive structures, nor among pods. It appears that the relative proportion of ¹⁴C allocated to any one pod, compared to other pods, depends on the dry weight of that pod as a proportion of the total reproductive dry weight. When the plant was growing actively, following the start of the reproductive phase until a few days before the end of flowering, the top of the plant (i.e., all the organs above the last opened flower) had a higher sink strength and a higher relative specific activity than pods, suggesting that it was a more competitive sink for assimilates. The pattern of assimilate distribution described here provides an explanation for pod and seed abortion.     

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     

A Flower and Pod Staging System for Soybean

Flower and pod abscission limit soybean yield. A system forquantifying flower and pod development based on the morphologicalappearance of the flower prior to and following anthesis hasbeen developed to aid in studies of pod abscission. Changesin the appearance of the corolla, primarily the banner petal,are used to distinguish the different stages of the system.External pistil dimensions have been correlated with internalfeatures for each stage of development. From anthesis to podset, pistil length and weight increase almost two- and fivefold,respectively, and ovule development progresses from unfertilizedegg cells to embryos surrounded by cellular endosperm. Pod determinedare correlated with ovule length and width and embryo cell number.Flower and pod stages can be determined in situ, thus permittingnon-destructive observation and experimental manipulation offlowers or pods without necessarily impeding their development.Stages have been identified that indicate precisely when podset occurs and when young pods cease growing and ultimatelyabscise. This system of flower and pod staging is useful instudies designed to assess effects of abiotic or biotic stressand genetic factors on pod set and abortion. Abscission, anthesis, Glycine max (L.) Merr, embryo development, pod set     

Preliminary studies on the effects of 4-chlorophenoxyacetic acid on the senescence and dehiscence of pods in oil seed rape (Brassica napus L.)

The auxin 4-chlorophenoxyacetic acid (4-CPA) has been found to delay the maturation and dehiscence of the pods of oil seed rape. Dipping pods in solutions of 500 gl^–1, 4-CPA, 36 and 39 days after anthesis delayed significantly the autolysis of the thin-walled parenchyma of the dehiscence zones, the senescence of the pod walls and the loss of water from the pod walls and seeds. Increases in both the fresh and dry weights of both pod walls and seeds were recorded in the treated pods as compared with controls.     

Effect of gibberellic acid on pod set in soybean

Field-grown soybean plants (Glycine max (L.) Merr. cv. Evans) were treated with gibberellic acid (GA₃; 10gl^–1) and/or (2-chloroethyl)-trimethylammonium chloride (CCC; 0.8gl^–1) in 1983 and 1984, and subsequent anthesis, pod set, seed size, seed number, and seed yield were determined at one node. The treatments were applied to five leaves in the center of each plant (typically leaves 7–11) and reproductive development at the node in the center of those leaves was monitored. Gibberellin A₃ applied Early (about 3d before anthesis of the first flower at the monitored node) had no effect on the number of flowers produced, but decreased the fraction of flowers that set pods in both experimental years (by 32% in 1983 and 76% in 1984). Seed size was slightly decreased by the GA₃ treatment in 1983 but not in 1984. The Middle GA₃ treatment (applied about 3 days after the Early treatment) slightly decreased the number of pods set; and Late treatments (9 days after) had no effect. None of the monitored parameters were affected by CCC.The Early experiments were repeated with two additional genotypes, Lincoln and T210. Genotype T210 is a single-gene, dwarf mutant of Lincoln whose stem elongation and leaf expansion are insensitive to GA₃. Gibberellin A₃ affected the reproductive parameters in Lincoln very similarly to Evans but those in T210 were unaffected. This indicates that GA₃ exerts its effect by increasing the mass of vegetative tissue and thus diverting assimilates away from the pods. However, since the mutation in T210 might affect a receptor that is in flowers as well as shoots, it is possible that GA₃ exerted its effect on the normal genotypes directly on the developing pods, rather than indirectly by diverting photoassimilates.     

The translocation of 14C photosynthate from leaves and pods in Phaseolus vulgaris

Field experiments were undertaken to study the pattern of distribution of photosynthate produced by the leaves and the pods of Phaseolus vulgaris (cv. Purley King) by means of the ¹⁴C technique. It was found that the ^UC photosynthate produced by a trifoliate leaf (38 days after anthesis) was shared almost equally between the leaf and the pod at its axil with 33–50% of the fixed ¹⁴C finding its way to the seeds in that pod. However, during the early stages of pod development (10 days after anthesis) some 13–14% of the fixed ¹⁴C was detected in the stem, indicating the inadequacy of the pod as a sink at that stage. When the pod was treated, virtually no ¹⁴C was detected in other parts of the plant. Of the ¹⁴C fixed by pod photosynthesis in the later stages (38 days after anthesis), 55–60% was translocated to the seeds within the same pod. These results indicate the importance of current photosynthesis during the pod fill stage in P. vulgaris as has been suggested in other grain legume crops.     

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.     

Distribution of 14C-sucrose applied to leaves at different nodes of okra (Abelmoschus esculentum) during flowering and early pod growth

The distribution pattern of ¹⁴C-sucrose from ¹⁴C-sucrose applied to vegetative okra plants and leaves 1–9 on separate plants during the green pod development stage were investigated in relation to duration and leaf position. Results indicated bi-directional transport of assimilates to both apical and basal portions of the stem. Within 48 h ¹⁴C moved to all plant parts; stem and leaves appeared to be strong sinks. In plants fed at the vegetative stage, 48 h after feeding, 66% of the fed activity was exported from the fed leaf. At the pod development stage, about 35% of the activity exported from the fed leaf was present in green pods and 65% in vegetative parts. In plants where leaf 1–9 was fed, irrespective of the position of the fed leaf, the subtending fruit was the strongest sink among the reproductive parts. Leaves and stems were the principal sinks.     

Mobilization of Minerals to Developing Seeds of Legumes

The mineral nutrition of fruiting plants of Pisum sativum L.,Lupinus albus L. and Lupinus angustifolius L. is examined insand cultures supplying adequate and balanced amounts of essentialnutrients. Changes in content of specific minerals in leaves,pods, seed coat, and embryo are described. P, N and Zn tendto increase precociously in an organ relative to dry matteraccumulation, other elements more or less parallel with (K,Mn, Cu, Mg and Fe) or significantly behind (Ca and Na) dry weightincrease. Some 60–90 per cent of the N, P and K is lostfrom the leaf, pod and seed coat during senescence, versus 20–60per cent of the Mg, Zn, Mn, Fe and Cu and less than 20 per centof the Na and Ca. Mobilization returns from pods are estimatedto provide 4–39 per cent of the seeds' accumulations ofspecific minerals, compared with 4–27 per cent for testatransfer to the embryo. Endosperm minerals are of only minorsignificance in embryo nutrition. Comparisons of the mineral balance of plant parts of Lupinusspp. with that of stem xylem sap and fruit tip phloem sap supportthe view that leaves and pod are principal recipients of xylem-borneminerals and that export from these organs via phloem is themajor source of minerals to the seeds. Endosperm and embryodiffer substantially in mineral compostition from phloem sap,suggesting that selective uptake occurs from the translocationstream during seed development. Considerable differences are observed between species in mineralcomposition of plant organs and in the effectiveness of transferof specific minerals to the seeds Differences between speciesrelate principally to Ca, Na and certain trace elements.     

花生衰老进程的研究

通过对鲁花11号和辐8707 2个高产花生品种的衰老进程研究表明：花生衰老具有地上部（叶片）渐进衰老和整株衰老的双重特点。花生从始花至花后60d左右为地上部（叶片）渐进衰老期：此期主茎高、侧枝长、分枝数、主茎、侧枝绿叶数、叶面积、茎、叶干重迅速增加,并接近或达到最大值,主茎及侧枝基部叶片逐渐由下向上开始衰老死亡,饱果开始出现,根系活力、固氮酶活性逐渐升高至接近最大值,始花后60－90d为整株缓衰期,此期地上部茎叶生长基因停止,逐渐开始衰老死亡,主茎、侧枝绿叶数开始减少,生殖体（荚果）干重迅速增长,根系活力、固氮酶活性缓慢降低;始花后90d以后称为整株速衰期,此期主茎、侧枝绿叶迅速减少,地上部迅速衰老死亡,生殖体（荚果）干重缓慢增长,根系活力、固氮酶活性迅速降低。地上部（叶片）渐进衰老期与开花及大量荚果形成相对应,整株缓衰期伴随着荚果迅速增重,整株速衰期与荚果缓慢增重一致。     

Effects of mixtalol and paclobutrazol on photosynthesis and yield of rape (Brassica napus)

Photosynthetic and yield effects of paclobutrazol and mixtalol sprayed, respectively, on rape at the three-leaf stage and shoot or anthesis stages were examined. They significantly increased chlorophyll content and photosynthetic rates, prolonged leaf longevity, and increased green pod area. Paclobutrazol-treated plants were shorter, more branched, and produced more seeds. Foliar sprays of mixtalol increased podding percentage, pods per plant, and seeds per pod. A high seed yield of 1809.0 kg/ha was obtained with mixtalol sprayed at anthesis, while significant yields were also achieved with treatments of mixtalol at the shoot stage and paclobutrazol at the three-leaf stage. The photosynthetic and yield effects of mixtalol or paclobutrazol were reduced when both growth regulators were applied together, and this led to yield reductions. No adverse effects from mixtalol or paclobutrazol were observed on seed oil content, erucic acid, and glucosinolate content. The total rape oil production with mixtalol sprayed at anthesis and shoot stages and paclobutrazol at the three-leaf stage increased significantly by 20.9%, 14.4%, and 13.4%, respectively, over the controls.     

Effects of Manipulations of Source and Sink on the Carbon Exchange Rate and Some Enzymes of Sucrose Metabolism in Leaves of Soybean [Glycine max (L.) Merr.]

Soybean plants [Glycine max (L.) Merr. cv. AGS129], two andthree weeks after depodding and defoliation, respectively, wereused to examine the possibility of end-product regulation onthe carbon exchange rate and activities of enzymes involvedin sucrose metabolism in leaves. Removal of one and two lateralleaflets per trifoliate leaf reduced the total leaf area by20% and 47%, respectively. Removal of one pod per node reducedthe total pod number by 23% per plant. Dry weights of roots,stems and petioles decreased with reductions in leaf area. Bycontrast, removal of pods resulted in an increase in these parameters.The carbon exchange rate and transpiration rate of leaves increasedwith defoliation and decreased with depodding. The intercellularconcentration of CO₂ in leaves was reduced by defoliation andincreased by depodding. Furthermore, defoliation increased thelevel of leaf chlorophyll in leaves while depodding decreasedit. Removal of pods decreased the activities of sucrose-phosphatesynthase and -amylase but increased that of sucrose synthase.A significant positive correlation was found between the activityof leaf sucrose-phosphate synthase and both the carbon exchangerate and the sucrose content of leaves. Thus, manipulation ofthe sink and source in soybean plants influenced the relationshipbetween sucrose metabolism and the carbon exchange rate in intactleaves. ³Faculty of Agriculture, Okayama University, Tsusimanaka Okayama,700 Japan ⁴Faculty of Agriculture, Saga University, Honjo-machi, Saga,840 Japan ¹Present address: Faculty of Agriculture, Sriwijaya University,J1 Raya Indralaya, OK1 30662, Indonesia ²Present address: Faculty of Agriculture, Saga University, Honjo-machi,Saga, 840 Japan     

Some effects of environmental stress on seed yield of cowpea (Vigna unguiculata (L.) walp.) cv. Prima

Summary Separate experiments examined nodulation and seed yield of cowpea cv. Prima after (a) changes in the level of combined nitrogen from 25 to 0 or 60 ppm N, (b) cycles of wilting and rehydration, and (c) shading to ca 50% full daylight. Plants were grown in the simulated tropical environment of a plastics bubble house and experienced these changes over the growth stages: emergence to first flower, first flower to mid pod-fill or mid pod-fill to maturity.Seed yields of nodulated plants were unaffected by combined nitrogen supply and almost double those of non-nodulated plants (100 g cf 56 g per plant)-due mainly to increases in pod number per plant and mean seed weight. Reducing the nitrogen level from 25 to 0 ppm N, especially between mid pod-fill and maturity, reduced seed yields of non-nodulated plants to 36 g per plant. At the first flowering stage, plants grown without combined nitrogen had nitrogenase activities less than 10% of those supplied with 25 ppm N; 60 ppm N at any stage of development more than halved nitrogenase activity when compared with plants supplied with 25 ppm.Repeated wilting prior to flowering markedly reduced seed yields compared with the unstressed controls (41 g cf 76 g per plant)-mainly by decreasing subsequent pod production. Nodule weight and nitrogenase activity per plant were also much reduced. Wilting after flowering did not reduce yield, and nitrogenase activity was less affected.Shading throughout, or from first flower onwards, reduced seed yield by about 25% because fewer pods were produced. All shading treatments significantly increased mean seed weight compared with unshaded controls (116–121 mg cf 105 mg).One of a series of papers describing work undertaken in a collaborative project with the International Institute of Tropical Agriculture, Nigeria, sponsored by the U.K. Ministry of Overseas Development.Soil Microbiology Department, Rothamsted Experimental Station, Harpenden, Herts.Soil Microbiology Department, Rothamsted Experimental Station, Harpenden, Herts.