Effect of High Temperature Stress at Anthesis on Grain Yield and Biomass of Field-grown Crops of Wheat

Spring wheat (Triticum aestivumL., ‘Chablis’) wasgrown under field conditions from sowing until harvest maturity,except for a 12-d period [70–82 days after sowing (DAS)coinciding with anthesis] during which replicated crop areaswere exposed to a range of temperatures within two pairs ofpolyethylene-covered temperature gradient tunnels. At 82 DAS,an increase in mean temperature from 16 to 25 °C duringthis treatment period had no effect on above-ground biomass,but increased ear dry weight from 223 to 327 g m^-2and, at 83DAS, reduced root biomass from 141 to 63 g m^-2. Mean temperatureover the treatment period had no effect on either above-groundbiomass or grain yield at maturity. However, the number of grainsper ear at maturity declined with increasing maximum temperaturerecorded over the mid-anthesis period (76–79 DAS) and,more significantly, with maximum temperature 1 d after 50% anthesis(78 DAS). Grain yield and harvest index also declined sharplywith maximum temperature at 78 DAS. Grain yield declined by350 g m^-2at harvest maturity with a 10 °C increase in maximumtemperature at 78 DAS and was related to a 40% reduction inthe number of grains per ear. Grain yield was also negativelyrelated to thermal time accumulated above a base temperatureof 31 °C (over 8 d of the treatment from 5 d before to 2d after 50% anthesis). Thus, grain fertilization and grain setwas most sensitive to the maximum temperature at mid-anthesis.These results confirm that wheat yields would be reduced considerablyif, as modellers suggest, high temperature extremes become morefrequent as a result of increased variability in temperatureassociated with climate change.Copyright 1998 Annals of BotanyCompany Triticum aestivum, spring wheat, temperature, grain number, grain yield, root growth.     

The Growth and Survival of Severely-shaded Tillers in Lolium perenne L.

The effect of shading a single tiller to below its compensationpoint for a period of 5 weeks in vegetative plants of Loliumperenne L. cv. S23, was studied in two different experimentseach employing two light regimes, one of which was common toboth experiments. In the first experiment tillers in the axils of the first leafwere shaded three weeks from appearance at both 40 and 70 Wm^–2. None of the shaded tillers died and they continuedto produce new leaves and increase in dry weight but at a reducedrate. In the second experiment, tillers with one emerged leafin any leaf axil position were shaded at 70 W m^–2 andin a treatment in which light was reduced to 13 W m^–2after initial growth at 70 W m^–2. As in the first experimentall shaded tillers survived at 70 W m^–2 but in the 70 13 W m^–2 transfer regime all shaded tillers died. In the second experiment shaded tillers in both light regimeswere supplied with ¹⁴C-assimilate by translocation from theremainder of the plant but in the 70 13 W m^–2 the initialsupport was withdrawn within 5 weeks of shading. The results are discussed in terms of the physiological relationshipsbetween the tillers of the grass plant. Lolium perenne L., growth of tillers, survival of tillers, effect of light     

Effects of CO2 Enrichment at Different Irradiances on Growth and Yield of Wheat: I. EFFECTS OF CULTIVAR AND OF DURATION OF CO2 ENRICHMENT

Wheat, Triticwn aestivum L., the winter cultivars Hobbit andCappelle-Desprez, and the spring cultivars Sicco and KJeiber,were grown in normal air or air enriched with CO₂ either outdoorsin a glass-roofed cage or in controlled environment rooms. Inneither the winter nor the spring wheat was growth increaseddue to enrichment with CO₂ before anthesis. Enrichment of thetwo winter wheat cultivars increased shoot dry weight significantlyat 15 d after anthesis but produced no significant increasein grain yield. With the spring cultivars there was a significantincrease in shoot dry weight by 18 d after anthesis and thegrain yield was also larger due to an increase in grain size.Shoot weight increased because the stems were larger, and therewas a diversion of assimilate from grain growth to late tillerproduction. Root tissue comprised less than 20% of the totaldry matter at anthesis (for all cultivars); effects of CO₂ enrichmenton root growth appeared to be less important than effects onshoot and ear growth. Growth and yield responses to CO₂ enrichmentwere observed (for the spring cultivars) at irradiances of both250 and 635 µE m^–2 s^–1, but the effects weregreater at the lower irradiance. Key words: CO₂ enrichment, Wheat, Cultivar     

Partitioning of Dry Matter and the Deposition and Use of Stem Reserves in a Semi-dwarf Wheat Crop

An experiment was carried out within a crop of spring wheat(cv. Condor) to examine dry matter partitioning between thedeveloping stem and ear, and to estimate the magnitude of carbonstored in the stem both before and after anthesis, and the subsequentutilization of these reserves during grain growth. The amount of reserve laid down and mobilized was estimatedfrom analysis of data for changes in masses of stem and leaffrom frequent harvests. The rate of change of the dry mass ofthe individual plant organs was expressed as a proportion ofthe rate of change of the total dry mass of the large culm.This value was called the Allocation Ratio (AR). It was assumedthat assimilate was transferred directly from the stem intothe growing ear, and not into other organs. This paper providesevidence for the idea that the stem intemodes of wheat are ableto accumulate and subsequently mobilize a dry matter reserve.The accumulation and subsequent mobilization of fructans inthe stem was demonstrated using ascending thinlayer chromatography.On a dry matter basis the large culms of the wheat crop accumulatedall of their stem reserves after anthesis (0–41 g perlarge culm; 98·4 g m^–1). After adjusting the lossof mass by 33% to allow for respiration, it was concluded thatpost-anthesis stem reserves may have contributed at least 21%of the final grain yield of this crop. Triticum aestivum L., semi-dwarf spring wheat, dry matter partitioning, stem reserves, fructans     

Effects of CO2 Enrichment at Different Irradiances on Growth and Yield of Wheat: II. EFFECTS ON KLEIBER SPRING WHEAT TREATED FROM ANTHESIS IN CONTROLLED ENVIRONMENTS IN RELATION TO EFFECTS ON PHOTOSYNTHESIS AND PHOTORESPI RATION

Spring wheat plants were grown in a cage with a glass roof untilthree days after anthesis and then subjected to treatments inconstant environment rooms with any one of all combinationsof four irradiances and two concentrations of carbon dioxide.The photoperiod was 16 h and day/night temperatures 19?C/14?C.Growth and yield of grain were saturated at the two brightestirradiances. Carbon dioxide enrichment from 350 to 1200 mm³dm^–3 increased shoot dry weight and grain yield at finalharvest at all irradiances, by averages of 10.5 (not significant)and 23.5 (significant) percent respectively. However, increasingthe irradiance from 150 to 613 µE m^–2 s^–1caused much larger yield increases (approximately 3-fold). Increasedgrain production by increased light was caused by both increasesin dry weight per grain and by increases in grain number perspikelet. The increase caused by CO₂ enrichment was mainly becauseof increased dry weight per grain. Increase in ear dry weightcaused by CO₂ enrichment took place between 30 and 60 d afteranthesis. The increase in shoot dry weight took place immediatelyafter exposure to increased CO₂ from 3 to 15 d after anthesis.Net photosynthesis by flag leaves on the main shoots was almostdoubled 16 d after anthesis by the CO₂ enrichment even thoughstomatal resistance was also doubled. However, this increasewas not reflected by a proportional increase in yield, probablybecause increased mutual shading by bigger stems and late tillersreduced total assimilation and because of increased respirationby the shoots. The increase in photosynthesis was not due toa decrease in photorespiration but to an increase in gross photosynthesis. Key words: CO₂enrichment, Photosynthesis, Photorespiration     

Effects of Temperature Variation at Different Times on Growth and Yield of Sugar Beet and Barley

Sugar-beet and barley were grown in pots outdoors (environmentN) and, for five successive 4-week periods starting at sowing,batches of plants were transferred to three growth rooms whosetemperatures were either similar to the outdoor mean (environment^M), or 3° C hotter (environment H) or 3° C colder (environmentC). Some plants were harvested immediately after treatment;others were returned to environment N and harvested when mature. At the end of period 1, sugar-beet plants from environment Mhad more dry weight and leaf area than those outdoors. Immediatelyafter spending later periods in environment M, plants had smallerleaves and similar dry weight to those continuously outdoors.These differences disappeared by maturity. Warmth in the growthrooms (i.e. the difference H—C) during periods 1, 2, and3, while leaf area was increasing, increased the number andsize of leaves and usually also dry weight; in later periodsit had no effect. The effects induced during periods 2 and 3,but not period 1, persisted to maturity to give greater totaland root dry weight and yield of sugar. The final effects ondry weight were much larger than those immediately after treatment,and were the result of differences in growth outdoors aftertreatment which depended on differences in leaf area; the efficiencyof the leaves was not affected by previous treatment. Transferring barley to environment M from N had inconsistentimmediate effects on leaf area and dry weight which disappearedby the final harvest. Transfer during periods 2 and 3, beforethe ears had started emerging, increased shoot number and delayeddevelopment. The proportion of the ears that ripened and theyield of grain were usually less for plants that had spent aperiod in environment M than for plants permanently outdoors,which also had some green ears. Warmth in the growth rooms duringperiods 1 and 2 increased dry weight and leaf area immediately,but had negligible effects at maturity because the increasesin leaf area did not persist after ear emergence. Warmth laterhastened death of leaves, decreased total dry weight immediatelyand also at maturity, but increased the proportion of ears thatripened and hence usually grain weight. Variation in leaf areaduration after ear emergence (D), determined by effects on thetime the ears emerged and the rate the leaves died, accountedfor most of the variation in grain yield, but warmth after theears emerged decreased grain yield less than proportionallyto the decrease in D. Net assimilation rate (E) of sugar-beet was greater than ofbarley, and decreased less with age. E of both species was usuallygreater in environment M than outdoors in spite of less radiation.It was only slightly affected by temperature. Nitrogen and potassium uptake were increased by treatments thatincreased dry weight. The percentage contents suggest that extrauptake was a consequence and not a cause of the increase indry weight.     

Grain Yield of Pennisetum americanum Adjusts to Nitrogen Supply by Changing Rates of Grain Filling and Root Uptake of Nitrogen

Coaldrake, P. D., Pearson, C. J. and Saffigna, P. G. 1987. Grainyield of Pennisetum americanum adjusts to nitrogen supply bychanging rates of grain filling and root uptake of nitrogen.–J.exp. Bot 38: 558–566. Pearl millet (Pennisetum americanum(L.)Leeke) was grown in containers at three constant rates of nitrogensupply or with the nitrogen supply increased from the lowestto the highest rate during panicle differentiation or at anthesis.We measured the rate and duration of nitrogen and dry weightgain by individual grains and nitrogen (¹⁵N) uptake by rootsand its distribution during grain filling. The total amountsof nitrogen and dry weight in all grain per plant at the lowestnitrogen supply were 8% and 14% respectively of plants growncontinuously at the highest rate of nitrogen. This was becauselow rates of nitrogen supply reduced grain number, mean grainweight and the nitrogen content of each individual grain. Theamino acid composition of the grain protein was affected onlyslightly by nitrogen treatments. Rates of grain growth were sensitive to nitrogen supply whereasthe duration of nitrogen movement to the grain was not. Nitrogenuptake by roots continued throughout grain filling; rates ofuptake per g root in plants given least nitrogen were one-halfthose of plants given the highest amount of nitrogen. A changefrom lowest to highest nitrogen supply at panicle differentiationincreased the uptake of nitrogen by roots and the rates of growthof individual grains, to the rates observed in plants whichhad been supplied continuously with the highest nitrogen. Whenthe change in supply was made at anthesis there was rapid movementof nitrogen into the plant but this was not translated intomore rapid grain growth. Key words: Nitrogen supply, Pennisetum americanum, grain yield, root uptake     

The duration and rate of grain growth, and harvest index, of wheat (Triticum aestivum L.) in response to temperature and CO2

Winter wheat (Triticum aestivum L. cv. Hereward) was grown inthe field inside polyethylene-covered tunnels at a range oftemperatures at either 380 or 684 µmol mol^–1 CO₂.Serial harvests were taken from anthesis until harvest maturity.Grain yield was reduced by warmer temperatures, but increasedby CO₂ enrichment at all temperatures. During grain-filling,individual grain dry weight was a linear function of time fromanthesis until mass maturity (attainment of maximum grain dryweight) within each plot. The rate of progress to mass maturity(the reciprocal of time to mass maturity) was a positive linearfunction of mean temperature, but was not affected by CO₂ concentration.The rate of increase in grain dry weight per ear was 2.0 mgd^–1 greater per 1 C rise, and was 8.0 mg d^–1 greaterat 684 compared with 380 µmol mol^–1 CO₂ at a giventemperature. The rate of increase in harvest index was 1.0%d^–1 in most plots at 380 µmol mol^–1 CO₂ andin open field plots, compared with 1.18% d^–1 in all plotsat 684 µmol mol^–1 CO₂. Thus, the increased rateof grain growth observed at an elevated CO₂ concentration couldbe attributed partly to a change in the partitioning of assimilatesto the grain. In contrast, the primary effect of warmer temperatureswas to shorten the duration of grain-filling. The rate of graingrowth at a given temperature and the rate of increase in harvestindex were only independent of the number of grains per earabove a critical grain number of 23–24 grains per ear({small tilde}20 000 grains m^–2). Key words: Winter wheat, grain growth, temperature, CO₂, harvest index, critical grain number     

The Fate of the Dry Matter, Carbohydrates and 14C Lost from the Leaves and Stems of Wheat during Grain Filling

In a field study with six winter wheat genotypes losses of drymatter from the stems between 30 June and maturity averaged172 g m^–2 (range 82–236), there being significantdifferences in loss between genotypes. Respiration from thestems during the same period was estimated to amount to 106g m^–2 (range 104–225). The amount of dry mattermobilized from the stems, calculated by difference, was estimatedas 66 g m^–2. The loss of ethanol- and water-soluble carbohydratefrom the stems (170 g m^–2; range 124–215) was verysimilar to the dry weight loss. Carbon-14 labelling was used to trace the time course and theamount of the movement of assimilates from the vegetative organsto the grain. Only 14•3 per cent (range 10•3–21•0)of the products of photosynthesis over the period 21 May-20June were relocated to the grains. This relocation amountedto an average of 7 per cent (range 5•7–11•4)of the final grain weight. It was estimated that during the18 days following anthesis on 20 June photosynthesis contributed48 per cent (range 39–55) of the final grain dry weight.Of this, about half was translocated to the grain within 10days of initial assimilation. The remainder appeared to be storedtemporarily in the stems and leaves and translocated to thegrains during the period 17–29 July. In general, relocationof dry matter from the vegetative organs to the grains, assessedby carbon-14 labelling, was greatest in those genotypes (Hobbitand Sportsman) which lost most dry weight from the stems andleaves.     

Growth, Development, and Yield of Spring Wheat in Artificial Climates

Spring wheat was grown to maturity in three growth rooms providing:(a) 18 h of light at 20° C and 6 h of darkness at 15°C (hot long days, HL); (b) 18 h of light at 15° C and 6h of darkness at 15° C (cold long days, CL); (c) 14 h lightat 20° C and 10 h of darkness at 15° C (hot short days,HS). Plants were moved between environments at spikelet initiationand anthesis, so dividing the growth period into three. Meanlengths in days of these periods in the different environmentswere: Period 1: HL 16, CL 18, HS 25; Period 2: HL 42, CL andHS 61; Period3: HL 53, CL 83, HS 63. The length of periods 2and 3 also depended on previous treatments. Grain dry weight was affected by environmental differences inall periods and effects in successive periods were additive.Compared with HL, CL or HS in period I before initiation increasedgrain yield by 6 per cent by increasing grain number per ear,HS in period 2 between initiation and anthesis decreased itby 24 per cent by decreasing the number of grains per spikeletand the proportion of spikelets that contained grain; CL inperiod 2 increased it by 21 per cent by increasing the numberof ears; CL in period 3 after anthesis increased it by 16 percent because leaves died later; HS in period 3 decreased itby 14 per cent because there was less radiation and hence lessphotosynthesis. Dry weight of shoot and root at maturity wasincreased by CL or HS in periods 1 or 2, and increased by CLand decreased by HS in period 3. The effects on final yieldof treatment during periods 1 and 2 were the consequence ofsimilar effects already produced at anthesis, and shoot androot dry weight changed little during period 3. The effects of environmental differences on grain dry weightcould not be explained by differences in leaf-area durationafter anthesis (D₃), except that CL in period 3 increased bothyield and D₃ but not proportionately, so that, as with HS inthe same period, grain: leaf ratio was decreased. Environmentaldifferences in periods 1 and 2 appeared to affect grain weightby altering the capacity of the ear to accumulate carbohydrates,determined by the number of grains per ear, rather than by alteringthe supply of carbohydrates, determined by D₃. There were some interactions between environments in differentperiods which were usually small compared with the main effects.     

The Effect of High Temperature at Different Stages of Ripening on Grain Set, Grain Weight and Grain Dimensions in the Semi-dwarf Wheat 'Banks'

Grain number in the wheat cultivar Banks was reduced by up to11 % with a rise in temperature from 21/16 °C to 30/25 °Cover a 10-d period immediately following first anthesis in general,the upper ‘d’ and ‘c’ florets were moreaffected by high temperature than the basal ‘a’and ‘b’ florets within a spikelet and florets fromthe upper spikelets were more sensitive than those lower onthe ear Grain weight and grain length at maturity were most affectedby a 10 d period of high temperature commencing 7–10 dafter anthesis However, if dry-matter accumulation between thestart of a treatment and grain maturity was used as a base forcomparison, the response was more uniform throughout development,with a peak in sensitivity 25 d after anthesis Although grainposition within an ear did not have a large effect on the responseto temperature, grains from the basal spikelets were more sensitivethan those from the apex, and the upper floret grains of a spikeletwere more sensitive to high temperature than those at the base There is a need to obtain, for a range of cultivars, more comprehensivedata on the effect of the timing and degree of temperature stressfollowing anthesis, for use in interpreting the response torising temperatures late in the development of the crop in thefield Triticum aestivum L, wheat, temperature, grain development     

The effect of tiller removal and tiller defoliation on competition between the main shoot and tillers of spring barley

In glasshouse and field experiments the source-sink relations of the main shoot of plants of spring barley were modified by tiller removal and tiller defoliation. Decreasing competition by tiller removal promoted the growth of the residual main shoot and its component parts, and the earlier tillers were removed the greater was the effect. Stem dry weight was increased four-fold in the glasshouse by early tiller removal and was doubled in the field experiment. The grain yield of the main shoot ear was increased by 26 – 30% by tiller removal compared with tillering control plants and this was due to larger grains in all spikelet positions. On the other hand increasing competition by regular tiller defoliation had relatively little effect on the growth and development of the main shoot in the glasshouse study, but in the field the main shoot grain yield was reduced by 10% compared with the control. The main effect of tiller defoliation was on the development of tillers. In the glasshouse tillers survived repeated defoliation, continued to be produced, and the majority produced grain but with fewer and smaller grains per ear than in control plants. Tiller growth was supported by the import of assimilate from the main shoot and this was accompanied by an increase in the photosynthetic rate of the main shoot leaves. In the field all defoliated tillers died within 4 wk. These responses are discussed in terms of the physiological interrelations between the main shoot and tillers.     

Effect of the Duration of the Vegetative Phase on Shoot Growth, Development and Yield in Pearl Millet (Pennisetum americanum (L.) Leeke)

Craufurd, P. Q. and Bidinger, F. R. 1988. Effect of the durationof the vegetative phase on shoot growth, development and yieldin pearl millet (Pennisetum americanum (L.) Leeke).–J.exp. Bot. 38: 124–139 The duration of the vegetative phase (DVP) in millet, whichis the major cause of variation in the crop duration, has markedeffects on the number of productive tillers per plant and onmainshoot (MS) and tiller grain yield. Daylength extensionswere used to vary the DVP and the effect on factors affectingpanicle (tiller) number per plant and panicle yield examinedin millet hybrid 841A x J104, grown in the field at Hyderabad,India. Tiller appearance, shoot leaf appearance and leaf area,and stem and panicle growth, in both MS and primary tillers(PTs), were monitored at frequent intervals over the season.At maturity grain yield per shoot was measured The concept of thermal time was used to describe shoot development.The rates of tiller appearance and shoot leaf appearance werelinearly related to thermal time and were not affected by DVPtreatments. The duration of the growth phase from panicle initiationto flowering (GS2) and from flowering to maturity (GS3) was320 and 390 degree days (°Cd), respectively. There was nodifference in rates of leaf or tiller appearance or developmentbetween MS and PTs. Tiller appearance, tiller leaf appearanceand tiller apical development all ceased at the same time inthe later initiated PTs, approximately 550 °Cd from sowing,shortly after rapid stem growth had begun. Tillers that didnot survive were all vegetative or in the early stages of reproductivedevelopment at this time The rate of accumulation of dry matter per plant was similarin all DVP treatments, but in the longer DVP treatments a greaterproportion of the dry matter was partitioned to the MS. Mainshootstem and panicle growth rates were increased by a longer DVP,as was grain yield on the MS, and these were related to increasedMS leaf area. Concurrently, growth rates and yields in laterinitiated tillers were reduced in relation to their leaf areas.Stem growth rate was proportionately increased more than paniclegrowth rate in the longer DVP treatments and this, combinedwith a longer duration of stem growth, resulted in greater stemdry matter at maturity and, therefore, in reduced harvest index.     

The Interdependence of Tillers in Lolium multiflorum Lam.--a Quantitative Assessment

Experiments were made to determine the extent of reciprocaltransfer of products (derived from the assimilation of ¹⁴CO₂)between various parts of the young vegetative grass plant (Loliummultiflorum Lam.). When individual laminae on different tillerswere supplied with ¹⁴CO₂, 47–64 per cent of the fixedcarbon was exported after 24 h. The principal sinks were theroot system and the shoot or tiller to which the fed leaf wasattached. Other tillers also received significant quantitiesof radiocarbon. When whole tillers were supplied with ¹⁴CO₂the percentage of fixed radiocarbon exported within 24 h rangedfrom 14–31 per cent. Of this, 50–74 per cent wasrecovered from the root system (except in the case of exportfrom the youngest tiller) but exchange of material between tillersalso occurred.A reciprocity diagram is presented and it is concludedthat despite the magnitude of the exchange no tiller showedan over-all net gain or loss. The main shoot and the tillersdiffered in the extent of their carbon exchange and in theirdegree of independence. The oldest daughter tiller of the mainshoot was the most independent and the main shoot most interdependent.     

Abscisic Acid Translocation and Influence of Water Stress on Grain Abscisic Acid Content

The movement of foliar applied [1-¹⁴C]abscisic acid (ABA) inwheat plants (Triticum aestivum L., cv. Kolibri) was investigatedat two stages of grain development (1000 grains, weight 19 and24 g dry matter). [1–¹⁴C]ABA seemed to be readily translocated within 12h into the developing grains as well as in other plant parts.A subsequent rapid metabolism took place leading to a decreasedactivity of the ABA-containing chromatogram fraction in theyounger plants 48 h after application. The metabolism seemodto be less intensive in the older grains, where the activityrunning with the ABA increased over 64 h. Treating the leaves of barley plants (Hordeum vulgare, L., cv.Union) 2 weeks after anthesis with a gentle stream of warm air(36° C) resulted in a significant increase in the ABA contentof all parts of the ear. The results mentioned above indicatethat this may be partially due to translocation from other partsof the plant such as the leaves.     

Effects of Ear Removal on Photosynthesis, Carbohydrate Accumulation and on the Distribution of Assimilated 14C in Wheat

Removal of an ear from a tiller of a wheat plant growing inthe field did not result in any marked change in the net photosyntheticrate of the subtending flag leaf, even during the period whenthe ear would normally have received large amounts of assimilatefrom the flag leaf. Following ear removal, there was an increasein the amount of ethanol-soluble and ethanol-insoluble carbohydratesin the remaining organs of the tiller. ¹⁴C labelling studiesshowed that a new pattern of translocation was established within2–3 days of ear removal, and the tiller exported assimilateto other tillers on the plant, and possibly to the roots.     

Effect of Salinity on Growth, Nodulation and Nitrogen Yield of Chickpea (Cicer arietinum L.)

Chickpea cultivar ILC 482 was inoculated with salt-tolerantRhizobium strain Ch191 in solution culture with different saltconcentrations added either immediately with inoculation or5 d later. The inhibitory effect of salinity on nodulation ofchickpea occurred at 40 dS m^–1 (34.2 mol m^–3 NaCl)and nodulation was completely inhibited at 7 dS m^–1 (61.6mol m^–3 NaCl); the plants died at 8 dS m^–1 (71.8mol m^–3 NaCl). Chickpea cultivar ILC 482 inoculated with Rhizobium strain Ch191^spcstrwas grown in two pot experiments and irrigated with saline water.Salinity (NaCl equivalent to 1–4 dS m^–1) significantlydecreased shoot and root dry weight, total nodule number perplant, nodule weight and average nodule weight. The resultsindicate that Rhizobium strain Ch191 forms an infective andeffective symbiosis with chickpea under saline and non-salineconditions; this legume was more salt-sensitive compared tothe rhizobia, the roots were more sensitive than the shoots,and N₂ fixation was more sensitive to salinity than plant growth. Key words: Cicer arietinum, nodulation, N₂ fixation, Rhizobium, salinity     

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     

The Effects of Light Intensity and External Potassium Level on Root/Shoot Ratio and Rates of Potassium Uptake in Perennial Ryegrass (Lolium perenne L.)

Loliun perenne L. (cv.S. 23) was grown on vermiculite in winterin a heated greenhouse for 8 weeks under factorial combinationsof two potassium regimes (nominally 6 parts/10⁶ and 156 parts/10⁶in Hewitt's solution) and three densities of artificially supplementedvisible radiation flux (36.1, 7.3, and 2.2 W m^–2). Growthand potassium uptake were studied through the calculation ofvarious growth functions from fitted curves. There was little effect of potassium treatment but the experimentalmaterial responded markedly to light. Leaf-area ratio in thethree treatments showed extreme plasticity in increasing from2–3 x 10^–2 through 6 x 10^–2 to 8–9 x10^–2 m² g^–1 as light intensity decreased. Correspondingdecreases in unit leaf rate, however, caused over-all reductionsin relative growth rate. Specific absorption rates for potassium (A_K, dry-weight basis)were strongly reduced at the lower light intensities but alsodisplayed complex ontogenetic drifts. Values of the allometricconstant, k (the ratio of root and shoot relative growth rates),decreased from c. 0.7 at 36.1 W m^–2 through c. 0.3 at7.3 W m^–2 to a value not significantly different fromzero (P < 0.05) at 2.2 W m^–2. In material grown under the two higher light intensities a constantinverse relationship was found between the mass ratio of rootand shoot and the corresponding activity ratio. The resultsconform to this model: Mass ratio = –0.001+45.0 (1/activityratio) where activity ratio is expressed as specific absorptionrate for potassium (in µg g root^–1 h^–1)/unitshoot rate (rate of increase of whole-plant dry weight per unitshoot dry weight, in mg g shoot^–1 h^–1). The implicationsof this relationship are discussed.     

The Uptake of Phosphate by Plants from Flowing Nutrient Solution: III. EFFECT OF CHANGED PHOSPHATE CONCENTRATIONS ON THE GROWTH AND DISTRIBUTION OF PHOSPHATE WITHIN PLANTS OF LOLIUM PERENNE L.

Perennial ryegrass (Lolium perenne L.) was grown from seed for29 d in flowing solution culture containing 0.1, 0.4 or 6.4mmol m^–3 P before the concentrations were changed (0.1and 0.4 raised to 6.4; 6.4 lowered to 0.4; controls unchanged)for an experimental period of two weeks to test the hypothesisthat after the seedling stage, the maximum rate of plant growthcould be sustained by a lower concentration of phosphate atthe root/solution interface than was necessary for the maximumrate of seedling growth. During the 29 d seedling period growthwas greatest on 6.4 mmol m^–3 P achieving 179 mg per plantdry weight compared with 122 and 26 mg on 0.4 and 0.1 mmol m^–3P respectively. During the experimental period growth on thetreatment 6.4 lowered to 0.4 mmol m^–3 P continued at thesame rate as the 6.4 control achieving 981 and 983 mg per plantdry weight respectively. Similarly growth of the treatment 0.4raised to 6.4 mol m^–3 P was unaffected by the change inconcentration and was comparable with the 0.4 control. Bothresults support the hypothesis for seedlings exceeding about100 mg per plant dry weight. In contrast the small plants ofthe treatment 0.1 raised to 6.4 mmol m^–3 P behaved similarlyto seedlings and responded rapidly to the increased concentrationof phosphate in solution, achieving high rates of phosphateuptake and increasing the growth of shoot more than the growthof root so that the ratio of root: shoot declined from 065 to0.34, a value similar to that for the seedlings grown on 6.4mmol m^–3 P. Key words: Lolium perenne L, Phosphate concentration, Seedling growth