The Effect of Flower Maturity and Harvest Timing on Floral Extract fromBoronia megastigma(Nees)

Development of floral organs during maturation of flower budsinto fully open boronia flowers is described. The petals andfunctional anthers attain their maximum size prior to the non-functionalanthers and the stigma. Organoleptic properties of the floralextract change with successive stages of bud development. Theconcentrations of extract and volatiles in the extract (% byf. wt) increase as buds mature, the extract concentration beinghighest in large buds and open flowers and the concentrationof volatile compounds being highest in open flowers. The rateof flower and extract development was measured. Yields of flowermaterial and floral extract per plant, and the concentrationof total volatiles including ß-ionone reach maximumlevels when 70% of flowers have reached anthesis. All measuredfactors decline after this point, except extract concentration(% of f. and d. wt) which is maintained up to 83% open flowers. Boronia megastigma(Nees); brown boronia; Rutaceae; flower development; floral extract; solvent extraction; ß-ionone; essential oils     

Emission of Volatiles From Brown Boronia Flowers: Some Comparative Observations

Extensive research has focused on the concentration of aglyconeswithin brown boronia (Boronia megastigma) flowers, however emissionof volatiles into the headspace above these flowers is not welldocumented. Using solid-phase microextraction (SPME) to trapvolatiles and GCMS analysis, we observed 23 volatiles in theheadspace above buds and flowers throughout flower maturation,above dissected floral organs and above whole plants held for36 h under either continuous light, continuous dark or 12 hlight:12 h dark:12 h light treatments. Fully-opened flowersemitted the most complex mixture of volatiles and in the greatestquantity, with a rapid decline in senescent flowers. Caryophyllene,humulene and bicyclogermacrene declined as flower buds matured;ß-ionone increased. From the individual floral organs,emission from the petaline anthers comprised 38% of total emissionsfrom the (calculated) ‘whole flower’, with 27% contributedby the petals and 10.5% by the stigma. Monoterpenes dominatedthe headspace from the calyx; dodecyl acetate, methyl jasmonateand (Z)-n-heptadec-8-ene were relatively predominant in emissionsfrom the androecium. ß-Ionone, the major floral volatilein brown boronia, dominated volatiles emitted from the stigma(87%). However, the relatively tiny petaline anthers, activein pollen production and high in carotenoids, contributed thegreatest overall amount of ß-ionone to emission fromthe whole flower. There were three different patterns in emissionof volatiles from plants in response to different light conditions:(1) emission patterns identical irrespective of light environment,with maximum emission in the ‘endogenous’ dark period,i.e. when the plant would normally have been in the dark (-pinene);(2) similar emission in all treatments, with an increase anddecline over a period of 26 h (5-acetoxy linalool, cyclic ß-ionone,dodecyl acetate and (Z)-n-heptadec-8-ene); and (3) emissionin all treatments but enhanced in the dark, with a 27.5 h periodin some cases (cyclic ß-ionone endoperoxide, dihydroß-ionone, ß-ionone, and ‘total volatiles’).Preliminary evidence is presented for endogenous control ofemission of a number of volatiles such as -pinene, with perhapsdiurnal control of others such as ß-ionone. Copyright2000 Annals of Botany Company Boronia megastigma, brown boronia, SPME, headspace, floral volatiles, ß-ionone     

Volatiles in Different Floral Organs, and Effect of Floral Characteristics on Yield of Extract fromBoronia megastigma(Nees)

The relative amounts of volatile compounds in the extract andheadspace from each floral organ were assessed in order to identifythe main organs for accumulation and emission. The mass of flowers/organs,the number/density of oil glands and yield of volatiles wereexamined for their relationship with extract yield, in clonaland non-clonal plants. Boronia flowers were divided into componentorgans and the solvent extractable product and headspace aboveeach organ type was quantified. The petals comprised 50% ofthe weight of the flowers, and the stigma 20%; however, thestigma contributed 70% of the total volatile compounds to extractfrom the whole flower. Proportionately more ß-iononeand dodecyl acetate were emitted from the stigma and anthersthan were contained in the extract, compared with other volatiles.The sexual organs are morphologically equipped for emissionof volatiles to attract pollinators. Between non-clonal plants, there was a lower coefficient ofvariation for extract yield than for values relating to extractcomposition, indicating that the former is more heritable thanthe latter. Variation between clonal plants was reduced comparedwith variation between non-clonal plants. The environment modifiesyield and quality of extract in clonal plants, indicating thatboth have relatively low heritability. No significant relationshipsbetween any floral characteristics and extract yield were found.Biosynthetic potential to accumulate extract is therefore ofprime importance, and the effect of environment on this potentialshould be the subject of future work. Boronia megastigma; brown boronia; Rutaceae; essential oils; flower; stigma; oil gland; ß-ionone     

Intraspecific Variation in Oil Components ofBoronia megastigmaNees. (Rutaceae) Flowers

Intraspecific variation in the oil composition ofBoronia megastigmaNees.(Rutaceae) was examined. Boronia absolute is extracted fromblossom primarily for use as a food additive. A major componentis ß-ionone andB. megastigmais one of the commercial,natural sources of this compound. Genotypes superior in productionof ß-ionone and low in monoterpene hydrocarbons weresought from natural populations in the south west of WesternAustralia as part of a breeding programme. Flowers were collectedfrom 25 plants in each of 29 different populations. Blossomwas extracted with ethanol and analysed using a gas liquid chromatographfitted with ionisation detectors. The contents of ß-ionone,dodecyl acetate, -pinene, ß-pinene and limonene inthe oil extract were compared. Intra-population variation wasas great as inter-population variation and no distinct chemotypeswere found. Considerable variation existed in the content ofcomponents. The highest ß-ionone content was 1787mg g^-1f. wt. Some genotypes contained all five components analysed,others lacked one or more of the monoterpenes: -pinene, ß-pineneor limonene. Principle components analysis indicated that contentsof ß-ionone and dodecyl acetate were associated andthat they were distinct from the content of the monoterpenes,which were associated with each other. Natural shading was associatedwith lower levels of monoterpenes but other oils were unaffected.Young plants contained less pinenes than older plants and oldplants contained the most dodecyl acetate. Vigorous plants producedmore pinenes. Red flowers contained the least ß-iononeand dodecyl acetate.Copyright 1999 Annals of Botany Company Boronia megastigma,boronia, Rutaceae, oil, -pinene, ß-pinene, limonene, ß-ionone, dodecyl acetate, monoterpenes, chemotypes.     

Flower and Volatile Oil Ontogeny in Boronia megastigma

The volatile oils of flowers of Boronia megastigma Nees. areimportant commercially but little has been published regardingtheir localization or the dynamics of their synthesis. In thisstudy we examined the histochemistry, anatomy and volatile oilcomposition of the floral organs of plants from a native populationby SEM. Lysigenous glands occurred in all organs except the stigma andandroecium and were associated with the presence of - and ß-pineneand limonene in tissue extracts. These compounds increased inconcentration throughout fruit development. Petals, stamens,staminodes and stigmas were glandular and contained phenolicdeposits, a dense cytoplasm and prominent intercellular spaces.Extracts of these tissues contained dodecanol, ß-iononeand dodecyl acetate, the concentrations of which were greatestat the time of stigma receptivity. The location and timing oftheir synthesis together with their biological activity suggeststhat these volatile oils may have a role in pollination.Copyright1995, 1999 Academic Press Boronia megastigma Nees., Rutaceae, essential oils, volatile oils, reproductive biology, -pinene, ß-pinene, limonene, ß-ionone, dodecyl acetate, heptadecene     

Disruption of an Ice-nucleation Barrier in Cold Hardy Azalea Buds by Sublethal Heat Stress

Ice nucleating barriers of undetermined composition are knownto occur in floral buds of several cold hardy species, includingAzalea. Fluorescence microscopy indicated the presence of phenolic-nchareas within hardy Azalea flower buds, which could be ice barriers.Hardy buds were subjected to a sublethal heat stress of 45 °Cfor 2 h to disrupt barrier integrity. Two hours after treatmentthe low temperature exotherms (LTEs) of flowers were observedusing differential thermal analysis (DTA). The LTEs of budsexposed to heat stress were either fewer in number and/or occurredat higher temperatures than in controls. Visual assay of theflowers following DTA confirmed that heat-stressed flowers werekilled at higher temperatures than control flowers. Heat-stressedbuds also have lower resultant hardiness compared to controlsas demonstrated by controlled freezing experiments. Acclimation, phenolics, resistance, stress     

Influence of Genotype, Plant Growth Temperature and Anther Incubation Temperature on Microspore Embryo Production in Brassica napus ssp. oleifera

Eleven F₁ hybrid genotypes of winter rape (Brassica napus ssp.oleifera) were used in a study of induction and growth of microspore-derivedembryos. Plants of each genotype were grown in controlled environmentsat either a constant 15°C or a constant 20°C, both witha 16 h photoperiod. Equal numbers of buds, approximately 2.5mm in length, containing uninucleate microspores were harvestedfrom each genotype and either pretreated (14 d at 4°C) ordissected immediately after harvest. Anthers were cultured onliquid medium based upon that of Murashige and Skoog (1962)and containing 8% sucrose, 0.5 mg dm^–3 naphthylaceticacid and 0.05 mg dm^–3 benzylaminopurine. Anthers fromequal samples of buds were incubated at 35°C for 0, 1, 2or 3 d before transfer to 30°C (21 d) and then 25°C.After a total of 42 d incubation, cultures were scored for thepresence of macroscopic embryos (1–2 mm in length) andfor the presence of anthers containing aborted embryoids whichhad not developed further. The results showed first that bud pretreatment completely inhibitedinduction and secondly that anthers of all genotypes had anabsolute requirement for a 35°C treatment (optimal duration2 d) in order to induce embryoid formation. In the great majorityof genotypes plants grown at 15°C provided more productiveanthers than plants grown at 20°C. However, within eachtreatment there were great differences both in the frequencyof anthers showing induced embryoids and of the final yieldof embryos. There was evidence that hybrids with a common parentresponded similarly under certain treatments. This confirmedthe importance of genotypic control for some components of embryoyield. Key words: Brassica napus, Rape, Anther culture, Pollen, Haploid     

Environmental Factors Controlling Flower Opening and Closing in aPortulacaHybrid

To examine flower opening and closing of aPortulacahybrid, flowerbuds were placed in darkness for 12 h (2030–0830 h) at20 °C and then exposed to various light-temperature conditions.Flower buds exposed to light at 25, 30 or 35 °C opened within1 h, and wilted 10–14 h later. Flower buds exposed tolight at 20 °C started to open after 4 h but opened slowlyand not completely. Flower buds subjected to 25, 30 or 35 °Cin darkness also opened rapidly, but did not reach full opening.Flowers opened at 30 °C in light, and partially closed andopened repeatedly in response to cycles of a 2-h exposure to20 °C and a 2-h exposure to 30 °C at any time between1000 to 1600 h. Similar phenomena were observed when the flowersopened at 30 °C in light and then were subjected to darknessand light alternately at 30 °C, although the effect of lightwas less obvious than that of alternating temperature. Floweropening and closing were not affected by relative humidity.These results indicate that a rise in temperature is requiredfor rapid flower opening in the buds kept at 20 °C, andthat light intensifies the effect of high temperature. Exposureto light without a temperature change delayed and slowed floweropening which was never complete. The involvement of an endogenousrhythm in flower opening byPortulacais indicated. Portulacahybrid, flower opening, flower closing, temperature shift, endogenous rhythm.     

Some Effects of Light Intensity, Daylength and Temperature on Flowering and Pollen Tube Growth in the Watermelon (Citrullus lanatus)

The effects of light and temperature on flowering and pollentube growth were studied in watermelon [Citrullus lanatus(Thunb.)Matsum. and Nakai, cv. Early Yates] plants grown in controlledenvironment cabinets. All female flowers were pollinated inone group of plants; none was pollinated in the other group. Temperature increase from 25 ^°C to 35 ^°C with daylengthof 14 h and light intensity of 32 klx caused increase in flowernumber per plant, proportion of male flowers, ovary length anddiameter, ovule number per ovary, rate of pollen tube growthand percentage of penetrated ovules at 24 hand 48 h after pollination.Very few flowers were produced at 40 ^°C, but there was ahigh proportion of male flowers. Increase in daylength from14 h to 24 h at 25 ^°C with light intensity of 32 klx alsoincreased number of flowers per plant, ovary length and diameterand number of ovules per ovary but sex expression and rate ofpollen tube growth were unaffected. Reduction in daylength from14 h to 8 hat 25 °C and light intensity of 32 klx and reductionin light intensity from 32 klx to 8 klx at 25 ^°C and 14h daylength both produced an increase in the percentage of immatureovules. The presence of fruit on the vine resulted in fewerflowers per plant and in reduced ovary legnth and diameter underall conditions tested. The results are discussed in relation to the fruiting responseof the plant.     

Shoot Apical Meristems of Picea sitchensis Seedlings Accelerate in Growth Following Bud-set

First-year seedlings of Picea sitchensis were induced to setbuds by transferring them from long days (17 h) to short days(10 h at 20 °C, 12 h night at 12 °C). After 20 shortdays, the seedlings stopped growing in height, the shoot apicaldomes began enlarging and the transverse growth rates of theshoot apical dome tissues increased. For about 25 days thereafterprimordia were produced faster within the developing buds thanat the apices of seedlings which had been kept in long daysto prevent bud-set. Accelerated primordia production after bud-setenables the largest possible buds to be formed during the frost-freeperiod before winter. Picea sitchensis, apical meristem, bud-set     

Partitioning of [14C]sucrose and Acid Invertase Activity in Reproductive Organs of Pepper Plants in Relation to Their Abscission Under Heat Stress

The effect of heat stress on processes related to carbohydratepartitioning was investigated in young bell pepper (Capsicumannum L. cv. Maor) plants in relation to abscission of theirreproductive organs at different stages of development. None of the reproductive organs abscised after 5 d in a normalday/night temperature regime (25/18 °C). With a temperatureregime of 35 °C day, 25 °C night, abscission occurredin only a small portion of the flower buds and none of the flowersand fruitlets. However, when temperatures in the day and nightwere reversed (25/35 °C, day/night) all the buds and someof the flowers abscised during that time period. The young fruitat the first node did not abscise under any temperature regime.The abscission rate of the flower buds was reduced under heatstress if the developing fruit at the first node had been removed. High temperature during either the light or dark periods reducedthe export of [¹⁴C]sucrose from the source leaf (fed for 48h with [¹⁴C]sucrose). Both heat stress and fruit presence reduced the relative amountof [¹⁴C]sucrose which was exported to the flower buds, flowersand roots. Likewise, these treatments reduced the concentrationof reducing sugars in the reproductive organs. Concomitantly,the heat stress and fruit presence on the first node reducedthe activity of soluble acid invertase in the flower buds andthe roots, but not in young leaves. Overall, the results show that heat stress causes alternationin sucrose distribution in the plant, but may also have specificeffects on metabolic activities related to sucrose import andutilization in flower buds and flowers which in turn may enhancetheir abscission. Bell pepper, (Capsicum annuum L. cv. Maor), abscission, acid invertase, heat stress, reproductive organs, sink leaves     

Partitioning of [14C]sucrose and Acid Invertase Activity in Reproductive Organs of Pepper Plants in Relation to Their Abscission Under Heat Stress

The effect of heat stress on processes related to carbohydratepartitioning was investigated in young bell pepper (Capsicumannum L. cv. Maor) plants in relation to abscission of theirreproductive organs at different stages of development. None of the reproductive organs abscised after 5 d in a normalday/night temperature regime (25/18°C). With a temperatureregime of 35°C day, 25°C night, abscission occurredin only a small portion of the flower buds and none of the flowersand fruitlets. However, when temperatures in the day and nightwere reversed (25/35°C, day/night) all the buds and someof the flowers abscised during that time period. The young fruitat the first node did not abscise under any temperature regime.The abscission rate of the flower buds was reduced under heatstress if the developing fruit at the first node had been removed. High temperature during either the light or dark periods reducedthe export of [¹⁴C]sucrose from the source leaf (fed for 48h with [¹⁴C]sucrose). Both heat stress and fruit presence reduced the relative amountof [¹⁴C]sucrose which was exported to the flower buds, flowersand roots. Likewise, these treatments reduced the concentrationof reducing sugars in the reproductive organs. Concomitantly,the heat stress and fruit presence on the first node reducedthe activity of soluble acid invertase in the flower buds andthe roots, but not in young leaves. Overall, the results show that heat stress causes alternationin sucrose distribution in the plant, but may also have specificeffects on metabolic activities related to sucrose import andutilization in flower buds and flowers which in turn may enhancetheir abscission. Bell pepper, (Capsicum annuum L. cv. Maor), abscission, acidinvertase, heat stress, reproductive organs, sink leaves. Bell pepper, (Capsicum annuum L. cv. Maor), abscission, acid invertase, heat stress, reproductive organs, sink leaves.     

Flowering of Contrasting White Clover Varieties in Relation to Temperature in Controlled Environments

Effects of temperature on floral initiation of ten white clovervarieties growing in controlled environments are described.Plants grown under long days (16 h) were subjected to constanttemperatures of 26, 18 and 10 ^°C. Relationships betweenmorphological and physiological traits and flowering were examined. Most plants flowered at the two higher temperatures but only10 per cent of plants flowered at 10 ^°C. Larger leaved typestended to produce more reproductive buds per stolon at the highertemperatures than did smaller leaved varieties. Of the floral characters studied, floret number was least affectedby temperature. Ovule number and peduncle length were greatestat 18 ^°C. Variation in, and absolute level of nectar secretionwas greatest at the highest temperature. Trifolium repens, white clover, flowering, temperature     

The Effect of Fruit Load, Defoliation and Night Temperature on the Morphology of Pepper Flowers and on Fruit Shape

The shape and regularity of bell pepper (Capsicum annuumL.)fruit are known to be determined at a very early stage of flowerdevelopment. Small, flattened fruit which are commonly parthenocarpicdevelop under low-temperatures (below 16 °C) from flowerswith enlarged ovaries. In such flowers self-pollination is notefficient because of the large distance between the stigma andstamens. Flower deformation of this kind is common during thewinter season. In the present study it was found that deformationsof flowers, similar to those found under low temperatures, wereinduced in 15 d by complete removal of fruit from plants growingunder night-time temperatures of 18 °C. Only flowers whichwere at the pre-anthesis stage at the time of fruit removalwere deformed by this treatment. Removal of leaves from thelower part of the plant (source leaves) partially reduced theeffect of fruit removal on the shape of the flowers and on subsequentfruit morphology. Fruit removal induced significant increasesin the concentrations of starch and reducing sugars, but notsucrose, in the flower buds. Likewise, flower buds of plantswhich grew under a night-time temperature of 12 °C containedmore carbohydrate than those which grew at 18 °C. Theseresults suggest that flower morphology in pepper is at leastpartly controlled by source-sink relationships. Assimilateswhich are normally transferred to developing fruit may be transported,upon fruit removal, to the flower buds which subsequently swell.A similar increase in assimilate translocation to flower budsmay occur under low temperatures, subsequently causing deformationof fruit.Copyright 1999 Annals of Botany Company Pepper, (Capsicum annuumL), flower shape, low temperatures, source-sink relationship, fruit shape, seeds, reducing sugars, sucrose, starch.     

Studies on the Fragmented Shoot Apex of Grapevine: III. A SCANNING ELECTRON MICROSCOPE STUDY OF ADVENTITIOUS BUD FORMATION IN VITRO

Scanning electron microscopy (SEM) was used to provide directevidence that shoots produced in vitro from fragmented shootapices of grapevine were adventitious in origin. The effectof temperature on the formation of the adventitious buds wasalso examined using SEM. At 27°C, shoot buds were initiatedby 31 d following fragmentation of the apex, while at 35°Cshoot initiation and multiplication were already well-advancedat only 18 d after the start of culture. At 38°C, apicalfragments quickly browned and died. After 25 d at 35°C,structures resembling inflorescence primordia were also visible.These did not occur in cultures at 27°C. The primordia laterdeveloped into multiple-branched tendrils, structures whichappear to be intermediate between tendrils and inflorescencesand have not been previously described.     

Development of Meristems of Weigela florida Variety 'Bristol Ruby' Following Reproductive Induction in Long Days

Weigela florida variety ‘Bristol Ruby’ has longday requirements for its growth and, in general, for its flowering.Vegetative development, floral initiation and floral organogenesisare described using scanning electron microscopy during photoperiodictreatment in long days, under controlled conditions. Flowering of axillary buds of cuttings has been studied. Theapex of Weigela at the vegetative phase is characterized bya very small hollow meristem. After 9 long days, the meristemenlarges and, after 12 long days, early axillary buds are initiatedin the axils of the leaves, which become bracts. When the numberof long days was increased, flowers were initiated in the budson the induced branches; first at the proximal part of the branchwhere development afterwards slowed down, then on the medianparts of the branch where development was accelerated. Two bracteoles are differentiated soon after floral initiation;first initiation of the calyx required 18 long days. Petals,stamens and ovary were rapidly initiated after that. Weigelaflowers are clustered; the inflorescence ceased growth by abortionof the terminal meristem or by formation of a terminal flower.In axillary buds of the fifth node the formation of the clusterwas completed about 20 days after the beginning of floral induction. Weigela florida ‘Bristol Ruby’, scanning electron microscopic analysis, vegetative meristem, floral development stages, long days induction     

Day and Night Temperature Control of Floral Induction in Stylosanthes guianensis var. guianensis cv. Schofield

Floral initiation in seedlings of Stylosanthes guianensis var.guianensis cv. Schofield grown at a photoperiod marginal forflowering (12–11.75 h) was promoted by a combination oflow day (25 °C) and low night (16 or 21 °C) temperatures,and completely inhibited by a 35 °C day temperature. Additionally,earliness of floral initiation under naturally decreasing daylengthwas negatively related to temperature regime over the range35/30 to 20/15 °C (day/night). Stylosanthes guianensis var, guianensis, flowering, temperature, photoperiod, short-day plant     

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     

Floral initiation of Pharbitis nil, a short-day plant, under continuous high-intensity light

Pharbitis nil, a short-day plant, initiated floral buds undercontinuous illumination at 23°C, provided that the lightintensity was kept at 16,000 lux or above. Stem elongation ofthe plants was strongly inhibited but leaves developed normallyunder this condition. (Received November 26, 1971; )     

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.