A Comparison of the Effects of Diurnal Variation in Light Intensity with Constant Light Intensity on Growth of Chrysanthemum morifolium cv. Bright Golden Anne

Rooted cuttings were grown in controlled environment cabinetsat two daily light totals (63 and 125 J cm^–2 day^–1)with the light intensity constant throughout the day or in stepsgiving the same daily light total Plants were sampled frequentlyover a period of 83 days by which time they were in full flower.A comparison of the various growth measures derived from theprimary data on leaf area, fresh and dry weight of the plantand its parts, and morphological and floral characteristics,revealed only negligibly small differences between results forconstant and stepped regimes The results for the constant regimeswere compared with other experiments earned out simultaneouslyin order to indicate the reproducibility of growth in independentcabinets having nominally the same conditions     

Further Effects of Light Intensity, Carbon Dioxide Concentration, and Day Temperature on the Growth of Chrysanthemum morifolium cv. Bright Golden Anne in Controlled Environments

In earlier work the effects of light intensity over the range31 to 250 J cm^–2 day^–1 and carbon dioxide concentrationfrom 325 to 900 ppm with 8-h days at 18.3 °C and 16-h nightsat 15.6 °C were described. The present paper is concernedwith three further experiments with light levels up to 375 Jcm^–2 day^–1 (which corresponds to the daily totalin a glasshouse in southern England in early May or August andthe intensity is approximately that of mid-winter sunshine),carbon dioxide concentration up to 1500 ppm, and day temperaturesof 18.3 to 29.4 °C. Final plant weight was increased by light over the range 125–375J cm^–2 day^–1 and by carbon dioxide over the range325–900 ppm, with positive interaction between them; thisinteraction was increased by raising the temperature to 23.9°C and somewhat more at 29.4 °C day temperature. Leaf-arearatio and specific leaf area were reduced by increasing eitherlight or carbon dioxide but there was little effect of temperature.Leaf-weight ratios were uniform within experiments but therewere small consistent differences between one experiment andthe other two which also affected leaf-area ratios. Mean unit leaf rate was scarcely affected by day temperatureover the range investigated. There were the usual increasesdue to increased light and carbon dioxide concentration anda consistent difference in absolute value between one experimentand the other two. These differences in mean unit leaf rateare illustrated in detail in the ontogenetic trend of unit leafrate and plant size. Lower unit leaf rates were to a considerableextent compensated for by increased leaf-area ratios in theusual way. Despite the substantial differences in day temperature the specificwater contents (g water g dry weight^–1) differed little,showing in the majority of cases higher values in the highertemperature for otherwise similar treatment combinations. Flower development was somewhat delayed at 23.9 °C day temperature,and substantially so at 29.4 °C. Lateral branch length wasincreased at 23.9 °C and excessively so at 29.4 °C.This reveals quite clearly that a temperature optimum for vegetativegrowth may not be the optimum for flowering performance norproduce a desirable plant shape. Despite the marked effects of temperature on rate of flowerdevelopment, the relationship between flower development andthe ratio of flower to total weight was the same for all treatmentcombinations in all three experiments and coincident with thatreported earlier. Gasometric determinations indicated that respiratory loss bythe whole plant was a smaller proportion of net photosyntheticgain at a temperature of 29.4 °C than at 18.3 °C andwas likewise a smaller proportion at 1500 ppm carbon dioxidethan at 325 ppm. If photorespiration of leaves is assumed tobe as great as their dark respiration, the respiratory lossesare in the range of 31–50 per cent of the gross gain.Greater rates of photorespiration would increase the proportionaterespiratory loss.     

The Effects of Light Intensity and Carbon Dioxide Concentration on the Growth of Chrysanthemum morifolium cv. Bright Golden Anne

Rooted cuttings were grown in controlled-environment cabinetsat daily visible light totals of 31, 63, 125, and 250 J cm^–28-h day^–1 and carbon dioxide concentrations of 325 and600 ppm. The experiment was repeated on another occasion withthe inclusion of a further carbon dioxide level of 900 ppm.A 5-h tungsten night break was used in the first week to delayflower initiation The plants in the various treatment combinationswere sampled by frequent small harvests for leaf area and freshand dry weights of leaf, stem, root, and flower, and also forvarious morphological features. Other growth measures were obtainedby manipulation of the primary data, including the fitting ofprogress curves. Plants were respaced at intervals to minimizemutual shading. There was an increase in total dry-matter production with increasinglight and carbon dioxide, with a small positive interactionbetween them. Plants in one experiment had a somewhat higherunit leaf rate and a lower leaf-area ratio, the latter beingdue to a slightly smaller leaf-weight ratio. The effects ofadditional carbon dioxide were largely accounted for by increasedphotosynthesis. Although there were substantial differencesin specific leaf area between treatment combinations withineach experiment, the leaf-weight ratio was little altered inthe period of vegetative growth. The inverse relationship betweenspecific leaf area and unit leaf rate showed a very similartrend for all combinations of light and carbon dioxide concentration.Leaf area was a linear function of absolute leaf water contentfor all treatment combinations within an experiment, but therewas a small significant difference between occasions. Flower development was extremely delayed in the lowest lightlevel and substantially delayed at the next higher level. Thenumber of leaves below the flower decreased with increasinglight level Flower weight increased with increasing light above63 J cm^–2 8-h day^–1 and with increasing carbon dioxideconcentration, there being a positive interaction between them The initial weight and leaf area of cuttings differed for thetwo experiments, and although the results on the two occasionswere in the same direction, their magnitudes were different.Some of the discrepancy was eliminated by expressing the variousgrowth measures as functions of plant dry weight, but therewas evidently a difference in the potential for growth of thetwo batches of cuttings. The plants which were initially smallerhad a higher average unit leaf rate which, due to a higher leafwater content, was not offset by a lower leaf area ratio.     

The Variation in Response to Light Intensity and Carbon Dioxide Concentration Shown by Two Cultivars of Chrysanthemum morifolium Grown in Controlled Environments at Two Times of Year

The growth of the cultivar Golden Princess Anne (G.P.A.) wasstudied in controlled announcement cabinets in a range of lightconditions (125–375 J cm^–2 8-h day^–1) andcarbon dioxide concentrations (325–1500 ppm) in all combinationsPlants obtained in January and grown from January to April showedgreater final total dry weight and flower dry weight at bothhigher light intensity and higher carbon dioxide concentrationwith a strong positive interaction between them, whereas plantsobtained in September and grown from September to December didnot respond much to increased carbon dioxide concentration andthere was only a small positive interaction with light intensity.The plants grown from January to April had larger final leafareas, larger mean leaf-area ratios due mainly to larger specificleaf areas, and higher mean specific leaf-water contents comparedwith September–December plants. Despite the differencein specific leaf-water content, leaf area was almost the samelinear function of absolute leaf-water content at both timesof year. The other vegetative parts also had higher specificwater contents throughout the January–April experimentand the lateral branches were longer when compared with thecorresponding values for September–December Flower developmentwas slightly faster in September–December and the plantsbore on average one flowering branch less compared with January–Aprilplants. Plants in the lower light and carbon dioxide conditions hadlower unit leaf rates, but for plants of similar total dry weightthe effects of this on dry-matter increment were partially offsetby larger leaf areas at both times of year. The January–Aprilplants had greater leaf areas than September–Decemberplants of similar unit leaf rate and total dry weight. The cultivar Bright Golden Anne (B.G.A ) showed effects whichwere in the same direction but smaller in magnitude, tendingto diminish the differences between the times of year For example,the positive interaction in total plant dry weight was smallerin January–April compared with G P A , but larger in September–December.Leaf area, leaf-area ratio, specific leaf area, specific watercontent of leaf, stem, and root, and lateral branch length,were all larger for B G A in corresponding treatment-combinationsin two January–April experiments than in a September–Decemberone, although the difference between the times of year was smallerthan for G.P.A except for leaf area which was relatively butnot absolutely smaller Dry-matter increment and leaf area showedan inverse relationship for plants of the same total dry weight,as in G P A. In January–April B G.A plants of similarunit leaf rate and total dry weight also had greater leaf areasthan in September–December but the differences were notso large as for G.P.A Total dry-matter production was slightlygreater for B.G.A. in January–April and considerably greaterin September–December compared with G P A , and at bothtimes of year B.G.A. was more leafy, with higher specific watercontents for the vegetative parts. It was not possible to determine the cause of the differencesin growth obtained at the two times of year. It could have arisenbefore the cuttings were removed from the stock plants, duringpropagation, or during the course of the experiments in thegrowth cabinets.     

The Effects of Light Intensity at Different Stages in Flower Initiation and Development of Chrysanthemum morifolium

Rooted chrysanthemum cuttings were raised in growth cabinetsat a ‘standard’, constant light level of 125 J cm^–2day^–1 and were induced to flower by giving daily cyclesof 8 h light followed by 16 h of uninterrupted darkness. Sampleswere transferred at weekly intervals to either a higher lightlevel of 375 J cm^–2 day^–1 or a lower light levelof 31 J cm^–2 day^–1 where they remained for 2 weeksbefore they were returned. It was shown that receptacle formationnormally began in the second week of inductive short-days (short-days8–14) and floret initiation in the third week (short-days15–21) when plants were grown throughout in the standardenvironment Receptacle formation was delayed and significantlymore leaves were formed below the flower if short-days 8–14were spent in low light. Transfer to high light for this periodhad no apparent effect Transfer to low light at the onset offloret formation retarded their further development and reducedthe total number of florets formed Transfer to high light atthis stage slightly increased the number of florets formed butdid not appear to affect their development. The data for stageof flower development after 11 weeks of growth reflected theseeffects of light level on the early development of the apex The total and flower dry weights of plants transferred to lowlight for 2 weeks were generally smaller than those of plantswhich had remained throughout in the standard condition Highlight only produced lasting increases in weight when the transferswere made during the later stages of growth. Most of the additionaldry matter formed at this time was accounted for in increasedflower weight The correlation between flower development andflower weight ratio previously found under constant environmentsalso applied to transferred plants except when the light levelwas changed for the last 2 weeks of growth; relatively highvalues of flower weight ratio were then obtained by transferto high light and relatively low values by transfer to low light.     

Growth Analysis of Sweet Pepper (Capsicum annuum L.): 2. Interacting Effects of Irradiance, Temperature and Plant Age in Controlled Conditions

A growth analysis was carried out with sweet pepper plants grownin a phytotron. Irradiance conditions were: 0.84 or 3.25 MJm^–2 in 8 h, 1.67 MJ m^–2 in 16 h and 2.51 MJ m^–2in 24 h. Temperatures applied were 25 or 21 °C during thephotoperiod in combination with 25, 21 and 17 or 21, 17 and13 °C respectively during the nyctoperiod. Highest values for leaf area and total dry weight were foundwhen applying 1.67 MJ m^–2 in 16 h, followed by 3.25 MJm^–2 in 8 h, irrespective of the temperature regime. Continuousirradiance ultimately resulted in leaf drop. A reduction inthe day temperature decreased leaf area and total dry weight.At a day temperature of 25 °C the dry weight increased withdecreasing night temperature when applying 3.25 MJ m^–2in 8 h. At a day temperature of 21 °C leaf area and dryweight were reduced when 17 or 13 °C were applied duringa 16 h nyctoperiod. Values for relative growth rate, net assimilation rate, leafarea ratio and leaf weight ratio strongly decreased with advancingplant age. The effects of irradiance treatment on RGR and NARwere analogous to those on total dry weight while the reversepattern was observed for the LAR. A decrease in day temperaturedecreased the RGR. The effects of night temperature exhibitedstrong interactions with day temperature and photoperiod. Theinfluence of temperature on RGR was largely mediated throughchanges in the LAR. The latter parameter was highly correlatedwith the specific leaf weight. Capsicum annuum L., sweet pepper, growth analysis, irradiance, temperature, plant age     

Effects of CO2-Enrichment on the Growth of Young Tomato Plants in Low Light

Carbon dioxide-enrichment of young tomato plants grown in controlled-environmentcabinets at low light intensity (14 cal cm^–2 day^–1,visible radiation) increased their net assimilation rates and,initially, relative growth-rates. Subsequently, the relativegrowth-rate fell to near the rate of non-enriched plants, owingto a fall in leaf-area ratio associated with an increase inleaf dry weight/area. Sowing non-enriched plants a few daysearlier to reach the same total dry weight would not have producedidentical plants. The effects of CO₂-enrichment to 1000 vpm could be simulatedby increasing light intensity by approximately one third exceptthat the plants had shorter internodes than those in extra CO₂.This was a morphogenetic effect of light since CO₂-enrichmentitself produced slightly shorter plants than controls for anequivalent total dry weight. CO₂-enrichment did not change the dry-weight distribution inthe plants and had little effect on rate of leaf produoctionor the number of flower primordia. There were no indicationsthat beneficial effects of CO₂-enrichment operated other thanthrough increased photosynthesis.     

Effects of Carbon Dioxide Concentration on the Growth of Callistephus chinensis cultivar Johannistag

Carbon dioxide enrichment to 600 ppm increased the amount ofdry matter produced by Callistephus chinensis plants in growthcabinets with negligible mutual shading over a period of 18weeks. Further enrichment to 900 ppm showed smaller and morevariable increases. These effects were the result of a higherunit leaf rate of the treated plants. The direct effect on unitleaf rate was partly offset by a reduction in leaf-area ratio,and this was due almost entirely to the effect on specific leafarea with hardly any effect on leaf-weight ratio. Carbon dioxideaccelerated flower development by about a week at 600 ppm andsomewhat less at 900 ppm. The proportion of the total plantweight in the form of flowers showed a similar trend with timein all treatments and the relationship between flower-weightratio and dry-matter content of flowers was likewise similarfor all treatments, with the highest dry-matter contents ofabout 19 per cent associated with the highest flower-weightratios of about 0.44 for mature flowers. Carbon dioxide enrichmentsignificantly increased the dry-matter content of leaves. Theefficiency of energy conversion based on incident light anda twenty-four-hour cycle of 8 h light and 16 h dark for smallplants of 140–300 mg total dry weight (leaf areas of 50–120cm²) was about 4.7 per cent for the 325 ppm treatment, 6.3 percent for 600 ppm, and 5.5 per cent for 900 ppm. By referenceto some further experiments on the growth of C. chinensis cultivarJohannistag in glasshouse conditions, considerable adaptiveresponse to high and low light intensity was also demonstrated.     

Development and Control of the Number of Flowers per Node in Pisum sativum L.

Non-dormant flower initials are laid down in the axils of successiveleaf initials as they are formed by the apical meristem of Pisumsativum L. In cultivars with a maximum capability of two flowersper raceme, the undeveloped flower meristem divides into twoportions. One forms the first flower and the other either developsinto a small protrusion on one side of the first flower or becomesthe second flower, depending on the prevailing environment.Flower development in conditions favouring single-flowered racemeswas advanced by one plastochron. Variation in the number offlowers per raceme occurs between cultivars and between environments.The number of double flowers formed was favoured by higher lightintensity (120 Js^–1 m^–2) and carbon dioxide concentration(330 µ11^–) and lower temperature (15°C). Incultivars producing more than two flowers per raceme, lowerlight intensity (60 Js^–1 m^–2) plus higher temperature(20°C) increased the mean number of flowers per raceme.Soluble sugar levels in all varieties were higher (36.05 mgeq glucose g^–1 fresh weight) in the low temperature/highlight environment than the high temperature/low light environment(14.80 mg eq glucose g^–1 fresh weight). The flowering potential and stability of 13 cultivars have beenassessed in controlled environment and in sowing date trialsin the field. A stable variety, which consistently producedtwo flowers per raceme, was identified in controlled environmentand its stability was maintained in field trials. A linear regressionof stability of flower number in the field on stability in controlledenvironment accounted for 89.6 per cent of the variance (P<5per cent), but the flowering potential in a sowing date experimentwas not related to temperature or radiation intensity.     

Effect of CO2 Concentration on Growth of Sugar-beet, Barley, Kale, and Maize

Increasing the concentration of CO₂ in the air from the usual300 ppm to 1, 000 ppm in growth rooms with temperatures of 20°C during the 16-h light period and 15° C during the 8-hdark period increased the total dry weight of sugar-beet, barley,and kale by about 5o per cent. A further increase in CO, concentrationto 3, 300 ppm increased dry weight slightly more. These effectsoccurred with light intensities ranging from 3.7 to II.6 caldm–² min–¹ of visible radiation supplied by a mixtureof fluorescent and tungsten lamps, and were only slightly greaterwith the brighter light. Extra CO₂ also increased leaf area,though relatively less than dry weight, and the number of barleyshoots but not of sugar-beet or kale leaves; it decreased leaf-arearatio, specific leaf area, and the ratio of tops to roots. Maizewas taller with extra CO₂. Net assimilation rates in 1, 000 and 3, 300 ppm CO₂ were about20 and 30 per cent respectively greater than in 300 ppm. Uptakeof CO₂ in the light by complete tops and single leaves alsoincreased with increase in CO₂ concentration. Photosynthesisof leaves of plants recently transferred to a new CO₂ concentrationdepended only on that concentration and not on the originalone. Doubling the light intensity from 3.7 to 7.7 cal dm–²min–¹ affected dry weight, leaf area, net assimilationrate, etc., similarly to a tenfold increase in CO₂ concentration.     

Effect of Photoperiod on Growth of Sugar Beet

Sugar beet grown in controlled environments were given similardaily amounts of visible radiation during three different photoperiodtreatments. Plants were given (a) 115 W m^–2 visible irradiancefrom fluorescent and tungsten lamps for 12 h; (b) 88 W m^–2of the same light for 16 h or (c) 115 W m^–2 from fluorescentand tungsten lamps for 12 h extended to 16 h with low intensity(3 W m^–2) incandescent light from the tungsten lamps only.Plant growth was increased similarly in both long day treatments[(b) and (c)] and dry weights were 25 per cent greater thanin the 12 h photoperiod (a) after 6 weeks. Leaf area was increasedby 18 per cent and net assimilation rate by 10 per cent in the16 h photoperiod at 88 W ^m–2 (b). By contrast, extendingthe photoperiod with 4 h of incandescent light (c) triggereda photomorphogenic increase in leaf expansion which increasedleaf area per plant by 47 per cent and leaf-area ratio by 12per cent.     

Carbon Dioxide Exchange of Spring-wheat in Relation to Age and Photon-flux Density at Different Growth Temperatures

CO₂-exchange rates (CER) of the sixth and the flag leaves oftwo spring-wheat varieties, Kolibri and Famos, were comparedusing an open-circuit infrared gas analysing system. Measurementswere repeated every two weeks starting when leaf blades werefully expanded. Single plants were grown in a controlled environmenthaving a photopuiod of 15 h and a day/night temperature of 24/19°C(H), 18/13 °C (M), and 12/7 °C (L) respectively untilapprox. 2 weeks after anthesis and at 18/13 °C until maturity.The photosynthetic photon-flux density (PPFD) at the top ofthe plants was 500 µE m^–2 sec^–1. During themeasurements PPFD was gradually reduced from 2000 to 0 µEm^–2 sec^–1 whereas the temperature was maintainedat the respctive growth-temperatures during the light period.The CER of the sixth leaf declined fairly similarly for bothvarieties, except for Kolibri where a faster decline was observedduring the first two weeks after full leaf expansion. The CERof the flag leaf declined more slowly than that of the sixthleaf. With the flag leaf of Famos, the decline was nearly linear,whereas with Kolibri it was very slow during the first few weeksbut rapid as the leaves further senesced. This pattern becamemore pronounced as the growth temperature decreased. The declinein relation to leaf age was much smaller at low PPFD than athigh PPFD during the same period. At full leaf expansion Kolibrireached higher maximum CER than Famos except at H. As the PPFDwas reduced the difference became smaller and at very low PPFDsuch as 50 µE m^–2 sec^–1 was reversed for thesixth leaf. Under optimum growth conditions maximum values ofCER were greater than 50mg CO₂ dm^–2h^–1 and PPFDfor light saturation was close to 2000 µE m^–2 sec^–1.A comparison between the actual CER and a fitted curve widelyused, PN=(a+b/l)^–1–DR, showed that the goodnessof fit strongly depends on cultivar, treatment and leaf ageas well as on the number and the level of PPFD from which datafor calculations are taken. Triticum aestivum, L., wheat, photosynthesis, photon-flux density, light response, carbon, dioxide exchange     

Acclimation of Tomato Leaves to Changes in Light Intensity; Effects on the Function of the Thylakoid Membrane

When young tomato plants grown in high light (400 µmolquanta m^–2s^–1 PAR) were transferred to low light(100 µmol quanta m^–2s^–1 PAR), non-cyclic electrontransport capacity was decreased and the rate of dark re-oxidationof Q^–, the first quinone electron acceptor of photosystemII, was decreased within 1–2 d. In contrast, the amountof coupling factor CF₁, assayed by its ATPase activity, decreasedmore gradually over several days. The total chlorophyll contentper unit leaf area remained relatively constant, although thechlorophyll a/chlorophyll b ratio declined. When young tomato plants grown in low light were transferredto high light, the ATPase activity of isolated thylakoids increasedmarkedly within 1 d of transfer. This increase occurred morerapidly than changes in chlorophyll content per leaf area. Inaddition, in vivo chlorophyll fluorescence induction curvesindicate that forward electron transfer from Q^– occurredmore readily. The functional implications of these changes arediscussed. Key words: Tomato, leaves, light intensity, thylakoid membrane     

Density Studies on Lupins: I. Flower Development

In an August-sown experiment the pattern of flower developmentwas followed for cv. Ultra (Lupinus albus L.) and cv. Unicrop(L. angustifolius L.) grown at low (10 plants m^–2) andhigh (93 and 83 plants m^–2, Ultra and Unicrop respectively)densities. Dry weight increase of flowers on the main-stem inflorescenceand first lateral below the main-stem were compared at differentfloral stages. Maximum flower weight was reached just priorto the open flower stage and remained constant or declined untila pod formed or abscission occurred. The time period betweenmaximum flower weight and pod formation or abscission was upto 10 days. Emergence of the inflorescence was earlier and thefirst flower of Ultra opened 10 days before Unicrop. Developmentof each terminal raceme (inflorescence) was acropetal, withpods having formed on lower flower nodes when terminal flowerswere still quite immature. Laterals forming the next generationof inflorescences grew from axillary leaf buds below an inflorescencewhile it was in full flower. Sources of competition from connectedreproductive and vegetative metabolic sinks are discussed. Lupinus spp., lupins, flower development, planting density     

Studies on the Expansion of the Leaf Surface: II. THE INFLUENCE OF LIGHT INTENSITY AND DAYLENGTH

The parts played by constant amounts of visible radiation perday and its two components—daylength and intensity—ininfluencing the growth of Cucumis sativus have been investigated.The amount of radiation per day had a far greater influencethan either of its components per se. Nevertheless, small significanteffects of photoperiod were found, leaf expansion and dry weightincrease being greatest at daylengths between 10 and 15 hr.rather than with longer days which, with similar daily totals,would be expected to give the greatest amounts of assimilation. Rates of leaf production and appearance were greatest with thehighest amounts of radiation, but the rates of expansion ofindividual leaves and their maximum areas were greatest withintermediate amounts of radiation. This response resulted inan optimum curve relating the leaf surface and the dry weightattained after a given period to radiation. The amount of radiationgiving the maximum leaf surface and dry weight decreased withage and with external nutrient supply, but at any one age washigher for increase in dry weight than for increase in leafsurface; stem and root tissues responded more to high radiationthan did the leaf surface. The net assimilation rate was a linearfunction of visible radiation over the range of 15–120cal. cm.^-2 day^-1 explored, the highest value of radiation usedrepresenting the intensity at which photosynthesis would beexpected to be maximal over a 12–15 hr. day. The inhibitory effect of high radiation on leaf expansion andthe resultant influence on the growth of the plant are explainedin terms of the number and intensity of ‘sinks’for carbohydrate and mineral nutrients within the plant.     

Effect of Nitrogen Supply on the Grass and Clover Components of Simulated Mixed Swards Grown under Favourable Environmental Conditions I. Carbon Assimilation and Utilization

Simulated mixed swards of Perennial Ryegrass (Lolium perenneL.) cv. S23 and White clover (Trifolium repens L.) cv. S100were grown from seed under a constant 20 °C day/15 °Cnight temperature regime and their growth and carbon economyexamined. The swards received a nutrient solution daily, whichcontained either High (220 mg l^–1) or Low (10 mg l^–1)nitrate N. Rates of canopy photosynthesis and respiration, and final drymatter yields were similar in the two treatments although theproportions of grass and clover differed greatly. The Low-Nswards were made up largely of clover. The grass plants in theseswards had high root: shoot ratios and low relative photosyntheticrates – both signs of N deficiency – and were clearlyunable to compete with the vigorously growing Low-N clover plants.These had higher relative growth rates and dry matter yieldsthan their High-N counterparts. In the High-N swards clovercontributed around 50 per cent to the sward dry weight throughoutthe measurement period despite having a smaller proportion ofits dry weight in photosynthetic tissue (laminae) than grassover much of it. The latter was compensated for, initially bya higher specific leaf area than grass, and later by a higherphotosynthetic rate per unit leaf weight. The results are discussedin relation to observed declines in the clover content of swardsafter the addition of nitrogen fertilizer in the field. Trifolium repens, white clover, Lolium perenne, perennial ryegrass, nitrogen, photosynthesis, carbon balance     

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     

Bl?tenbildung bei Lemna paucicostata 6746 durch kombinierte Anwendung von Abscisins?ure und GCG

To a certain extent the flowering of Lemna paucicostata 6746is evoked in continuous light by application of abscisic acid(ABA) and CCC. Moreover, the action of the combined substancesappears in two separate concentration ranges. In the range ofABA 2?10^–9 M/CCC 10^–7–10^–6 M floweringis initiated without inhibition of vegetative growth and proceedsonly in the presence of high intensity light and sucrose. Acombination of ABA 2?10^–5 M/CCC 10^–3M simultaneouslycauses a strong inhibition of frond multiplication. Here theeffect can be observed also under low intensity light conditionsand without sucrose in the medium. A range with flower inhibitingactivity lies between the two flower promoting concentrationranges. (Received November 16, 1972; )     

Frond and flower production in Lemna gibba G 3 in presence of respiratory inhibitors

Effects of respiratory inhibitors on frond and flower productionin light culture of a long-day duckweed, Lemna gibba G 3, wereinvestigated. The inhibitors examined could be divided into3 groups based on their specific actions: (A) 2,4-Dinitrophenol(10^–6M), arsenate (10^–4M), malonate (10^–2M),o-phenanthroline (10^–6M), ,'-dipyridyl (10^–5M) andazide (10^–6M) inhibited flower production by suppressingthe rate of flower production without affecting the inductionperiod. Frond production, however, was promoted by these reagents.Effective time of application came one day after the end ofthe induction period. (B) Iodoacetate (10^–6M) and fluoride(10^–4M) inhibited both flower production and, less significantly,frond production. Reduced rate of flower production was responsiblefor the inhibition of flowering. Effective time of applicationpreceded by one day that of A group inhibitors. (C) Salicylaldoxime(10^–6M), diethyldithiocarbamate (10^–6M) and 8-hydroxyquinoline(10^–7M) enhanced flower production by reducing the lengthof the induction period, and simultaneously slightly inhibitedfrond production. Effective time of application was the latterhalf of the induction period. The implications of these findingsare discussed with special reference to the component processesinvolved in photoperiodic induction of flowering in duckweed. (Received March 27, 1969; )     

The Growth and Development of the Wheat Apex: The Effects of Photoperiod on Spikelet Production and Sucrose Concentration in the Apex

Spring wheat (Triticum aestivum cv. Warimba) plants were grownin a controlled environment (20°C) in two photoperiods (8or 16 h). In the first instance, plants were maintained in eachof the photoperiods from germination onwards at the same irradiance(375 µE m^–2 s^–1). In the second case, allplants were grown in a long photoperiod until 4 days after double-ridgeinitiation when half the plants were transferred to a shortphotoperiod with double the irradiance (16 h photoperiod at225 or 8 h at 475 µE ^–2 s^–1). The rates of growth and development of the apices were promotedby the longer photoperiod in both experiments. Shoot dry weightgain was proportional to the total light energy received perday whereas the dry weight of the shoot apex increased withincreasing photoperiod even when the total daily irradiancewas constant. The principal soluble carbohydrate present in the shoot apexwas sucrose, although low concentrations of glucose and fructosewere found in the apices of long photoperiod plants late indevelopment. Sucrose concentration was invariably greater inthe slow-growing apices of short photoperiod plants, but roseto approach this level in the long photoperiod plants when theterminal spikelet had been initiated. Triticum aestivum, wheat, apex, spikelet initiation, photoperiod, flower initiation