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     

Effects of temperature on the flowering and seed production of Stylosanthes guianensis cultivars

Seedlings of Stylosanthes guianensis var. guianensis were grown for 75 days in 16 h photoperiods and transferred to controlled environment cabinets for a further 112 cycles set at 12 h days and 18, 21, 24 or 27 OC constant temperatures. Floral initiation (FI) occurred in cv. Cook after 21 short-day cycles of 12 h and was independent of temperature. Warm temperatures delayed FI in cv. Schofield and hastened it in cv. Endeavour. Rate of node appearance was positively and the duration of the phase FI to flower appearance negatively related to temperature. Spike production and floret number per spike were maximal for Cook and Endeavour at 24°C; seed setting was independent of temperature above 18°C in Cook. Growth, flowering, and seed production of Endeavour required warm temperatures, but Cook was more versatile in its adaptation to varying temperature regimens.     

Flowering of Stylosanthes guianensis in Relation to Juvenility and the Long-Short Day Requirement

Seedlings of Stylosanthes guianensis var. guianensis were grownin long (14 h) days in five temperature regimes for varyingperiods before transfer to short (11 h) days at 30 ?C/21 ?C.The juvenile phase before seedlings responded to inductive conditionswas c. 45–50 d, 50–60 d and 60–70 d for cv.Schofield, cv. Cook and C.P.I. 34906 respectively, which ispositively related to their critical photoperiod for flowering.Temperatures favourable for growth (e.g. 30 ?C/26 ?C) reducedthe juvenile phase in C.P.I. 34906 and in Cook, which did notflower in 11 h days unless previously exposed to more than 18long days. In a second experiment cv. Cook was confirmed as a long-shortday plant. Seedlings were grown for 50 d in a glasshouse withnatural daylength extended to 13, 14, 16 or 24 h before transferto 12 h photoperiods. Cook floral development was positivelyrelated to daylength provenance before transfer and plants incontinuous 12 h did not flower. Shortening daylength after 48 cycles of 12 h to 11.75 h didnot result in continued floral development in Cook plants butcv. Graham plants were initiated or transitional by 75 d. Key words: Stylosanthes guianensis, Photoperiod, Temperature, Flowering     

Time of sowing and temperature effects on the flowering of Stylosanthes guianensis

Seedlings of Stylosanthes guianensis var. guianensis cv. Cook and of two selections of S. guianensis var. pauciflora (CIAT 1280 and CIAT 1062) were grown at day/night temperatures of 20°/25°, 30°/25°, and 35°/30°C in a naturally-lit glasshouse at latitude 27°30'S. Sowings were made in decreasing daylength at 30-day intervals from 22 January to 21 May. Cv. Cook and the CIAT 1280 selection did not flower fully if sown after 22 January and the CIAT 1062 selection did not flower if sown after 22 March. This is interpreted as a long-short day flowering response. Usually, flowers were initiated earlier and at a lower node at 25?/20°C than at the warmer temperatures. At 25?/20°C the first flowers to appear were produced predominantly at the terminal apex of the main stem in cv. Cook and the CIAT 1062 selection, but not in the CIAT 1280 selection. At the two warmer temperatures first flowers were more commonly produced at the terminal apex of primary, secondary and tertiary branches. There were more inflorescences per plant on earlier than later sown plants when measured 21 days from appearance of the first flower and the most inflorescences were produced by cv. Cook at 25?/20°C, by selection CIAT 1062 at 30°/25°C, and by CIAT 1280 at 35°/30°C.     

Development of Floral Apex After Floral Induction in Stylo (Stylosanthes guianensis (Aubl.) Sw. var. guianensis)

The apex morphology of stylo (Stylosanthes guianensis var. guianensis)is described in four developmental phases (vegetative, transitional,initiated and floral) further subdivided into a total of tenstages. The apical dome broadens and flattens as induction proceedsuntil the initiation phase when apical diameter within 0.05mm of the dome apex is 55 per cent greater than in the vegetativeapex. Changes in vegetative morphology during induction aredescribed. Stylosanthes guianensis var. guianensis, stylo, flowering, reproductive anatomy, developmental stages     

Effects of Temperature, Photoperiod and Seed Vernalization on Flowering in Faba Bean Vicia faba

Factorial combinations of three photoperiods (10, 13 and 16h), two day temperatures (18 and 28 °C) and two night temperatures(5 and 13 °C) were imposed on nodulated plants of six diversegenotypes of faba bean (Vicia faba L.). Plants were grown inpots in growth cabinets from both vernalized (1.5±0.5°C for 30 d) and non-vernalized seeds. The times from sowingto the appearance of first open flowers (f) were recorded. Seedvernalization decreased the subsequent time taken to flowerin almost all genotype x growing environment combinations (theexceptions were plants of the cv. Maris Bead grown in threecooler, short-day regimes). The influence of temperature andphotoperiod on the rate of flowering was quantified, using amodel applied previously to other long-day species of grainlegume in which positive linear relations between both temperatureand photoperiod and the rate of progress towards flowering areassumed to apply. A significant positive linear response ofrate of progress towards flowering to limited ranges of meandiurnal temperature was detected in all six genotypes, but inthree genotypes (Syrian Local Large, Aquadulce and Maris Bead)the 28 °C day temperature reduced the rate of progress towardsflowering - suggesting that the optimum temperature for floweringin these genotypes is below 28 °C. In four genotypes (MarisBead, Giza-4, Aquadulce and BPL 1722) a significant positiveresponse to photoperiod, typical of quantitative long-day plants,was observed only in plants grown from vernalized seeds. Incontrast, plants of the genotype Zeidab Local grown from bothnon-vernalized and vernalized seeds showed the same positiveresponse to photoperiod, whereas plants of the land-race SyrianLocal Large were consistently unresponsive to photoperiod. Theimplications of this range of responses amongst diverse genotypesare discussed in relation to screening germplasm. Vicia faba, faba bean, flowering, photoperiod, temperature, seed vernalization, germplasm screening     

Temperature Dependence of Viability and Dormancy of Zizania palustris var. interior Seeds Stored at High Moisture Contents

Seeds (caryopses) of North American wild rice (Zizania palustrisvar. interior), a temperate aquatic grass, have been thoughtto require storage at low temperatures and high moisture contentsto preserve viability. The seeds are also deeply dormant atmaturity and require up to 6 months of stratification to breakdormancy. We report here that wild rice seeds can retain viabilityat moisture contents 30% (f. wt. basis) for up to 6 monthsat temperatures as high as 30 °C, and for at least 1 yearat temperatures below 20 °C. Dormancy is not broken at temperaturesabove 10 °C, but subsequent stratification requirementsare unaffected by prior warm storage. Cold storage is thereforenot required to maintain viability of wild rice seeds, but isnecessary to break dormancy. Hydrated wild rice seeds can befrozen to –10 °C without damage, but dormancy is notlost at subfreezing temperatures. These results provide newoptions for long-term storage of wild rice seeds. Zizania palustris var. interior (Fassett) Dore, wild rice, seed, germination, dormancy, storage, moisture content     

Low Temperature Effects on Early Vegetative Growth, Leaf Gas Exchange and Water Potential of Chilling-sensitive and Chilling-tolerant Crop Species

Two chilling-sensitive (Phaseolus vulgaris L., Zea mays L.)and two chilling-tolerant (Pisum sativum L., Spinacia oleraceaL.) species were raised in growth chambers under warm (28/18°Cday/night cycle) and cool (18/12°C) temperature regimes.Growth analysis techniques were used to evaluate leaf area andbiomass partitioning during early autotrophic growth. Plantsacclimated to both temperatures were measured for leaf gas exchangeand water potential (     

Changes in Ultrastructure and Abscisic Acid Level, and Response to Applied Gibberellins inTaxus maireiSeeds Treated With Warm and Cold Stratification

Seeds ofTaxus maireiare known for their deep dormancy whichcan only be broken by a procedure involving warm stratificationfollowed by cold stratification. Treatments with alternatingtemperatures of 25/15 or 23/11 °C (12 h light) for 6 monthsfollowed by 5 °C for 3 months were successful in overcomingseed dormancy. After 6 months of warm stratification, cytologicalchanges observed included: enlargement of the embryo; a decreasein the number of lipid bodies; appearance of ER; and increasesin mitochondria, plastids, dictyosomes, vacuoles and microbodiesin the shoot apical meristem. Cold stratification followingthe warm treatment induced cell division, and one or two distinctnucleoli in the shoot apical meristem cells were observed. Bothwarm and cold stratification reduced endogenous ABA concentrationsfrom the original 8888 pg per freshly harvested seed to 392and 536 pg, respectively. Treatment with exogenous gibberellinsafter seeds had been warm-stratified showed that GA₄and GA₇wereeffective at promoting seed germination, but GA₃was not. Theseresults suggest that the strong seed dormancy ofT. maireicouldbe caused by a high ABA content and underdevelopment of theembryos in freshly shed seeds. We conclude that warm stratificationwith alternating temperatures increases the growth of embryosby cell expansion and enlargement and decreases ABA content,but seeds still remain ungerminated. Cold stratification mayinduce the response to GAs and initiate cell division resultingin release from physiological dormancy and subsequent germinationofT. maireiseeds.Copyright 1998 Annals of Botany Company Taxus mairei; ultrastructure; abscisic acid; gibberellin; seed dormancy; stratification; germination.     

Dormancy and Flowering in Anemone coronaria L. as Affected by Photoperiod and Temperature

The effects of day-length and temperature on flowering and dormancyinduction were studied in Anemone coronaria L., with plantsraised either from corms or achenes. An Israeli hybrid sourcewas used (de Caen cv. Hollandia x Israeli wild type). Dormancy onset is characterized by the cessation of foliageleaf production, the appearance of leaf scales protecting theperennating bud, and leaf senescence. Dormancy was induced byhigh temperature and long days but increasing temperatures (from17/12 °C to 32/12 °C) induced earlier dormancy thanprolonging the photoperiod (range 8–16 h). A significant(P = 0.01) interaction was found between these factors, withsmaller photoperiodic effects the higher the temperature. At22/17 °C the critical day-length for dormancy inductionwas between 11 and 12 h. The transition from the vegetative to the reproductive stageappears to be an autonomous process that occurs with developmentin plants raised from either corms or achenes and does not requireenvironmental induction. Photo- and thermoperiodic effects onflowering were indirect, being mediated through their influenceon dormancy induction. Anemone coronaria L., dormancy, flowering, photoperiod, thermoperiod     

Effects of Irradiance and Temperature on Flowering of Chrysanthemum morifolium Ramat. in Continuous Light

The short-day plant Chrysanthemum morifolium cv. Polaris initiatedflower buds in all irradiances of continuous light from 7.5to 120 W m^–2. As the irradiance increased, the transitionto reproductive development began earlier and the number ofleaves initiated before the flower bud was reduced. The autumn-floweringcultivars Polaris and Bright Golden Anne, and the summer-floweringGolden Stardust were also grown in continuous light at differenttemperatures; all initiated flower buds at temperatures from10 to 28 °C but only the buds of Golden Stardust developedto anthesis and then only at 10 and 16°C. Flower initiationbegan earliest at 16–22 °C, and the number of leavesformed before the flower bud was increased at 28°C. GoldenStardust was exceptional in that the number of leaves formedwas also increased at 10 °C. Axillary meristems adjacentto the terminal meristem initiated flower buds rapidly at 10°C but not at 28 °C in all three cultivars. These resultsare discussed in relation to the autonomous induction of flowerinitiation and the effects of the natural environment on floweringof chrysanthemum. Chrysanthemum morifolium Ramat, flowering, irradiance, temperature     

Thermosensitivity in Spring White Lupin

Spring morphotypes of white lupin (Lupinus albus L.) are veryresponsive to cool temperatures during seedling developmentas expressed in a number of subsequent developmental characters.Thermosensitivity was examined in a number of studies whereseedlings were incubated at various stages of development andat differing temperatures. Plants were scored for thermosensitivity,as expressed by the number of mainstem and first order lateralvegetative nodes, at flowering. The stages of radicle emergenceand split seed coat were observed to be the developmental stageswhen mainstem and first-order lateral meristems were most sensitiveto incubation temperature. These data show that the optimumwindow for cold treating spring lupin seed is very narrow andoccurs prior to seedling emergence. Seedlings at radicle emergencestage were incubated at temperatures ranging from 1 to 27 °Cfor 0 to 14 d in 2 d increments. For temperatures less than12 °C, mainstem node number decreased curvilinearly withduration of incubation. For temperatures between 12 and 17 °C,mainstem node number decreased linearly with duration of incubation.However, mainstem node number increased linearly with durationof incubation at temperatures greater than 17 °C. The datashow that 'warm' temperatures during early seedling developmenthave a profound influence on subsequent plant morphology. Responseto 'warm' temperatures is greater than to 'cool' temperaturesand it is suggested that the differential response to warm vs.cold incubation temperatures could account for morphologicaland phenological differences observed within genotypes in fieldstudies among sites and years. The lack of temperature responsein one genotype, 'Start' may indicate thermoneutrality in thisgenotype.Copyright 1995, 1999 Academic Press Lupinus albus L., lupin, vernalization, thermosensitivity, vegetative development     

Effects of Low Temperature on Growth and Nutrient Accumulation in Rye (Secale cereale) and Wheat (Triticum aestivum)

Rye (Secale cereale cv. Rheidol) and wheat (Triticum aestivumcv. Mardler) were grown at shoot/root temperatures of 20/20°C (warm grown, WG plants), 8/8 °C (cold grown, CG plants)and 20/8 °C (differential grown, DG plants). Plants fromcontrasting growth temperature regimes were standardized andcompared using a developmental timescale based on accumulatedthermal time (°C d) at the shoot meristem. Accumulationof dry matter, nitrogen and potassium were exponential overthe time period studied (150–550 °C d). In rye, therates of plant dry matter and f. wt accumulation were linearlyrelated to the temperature of the shoot meristem. However, inwheat, although the rates of plant dry matter and f. wt accumulationwere temperature dependent, the linear relationship with shootmeristem temperature was weaker than in rye. The shoot/rootratio of rye was stable irrespective of growth temperature treatment,but the shoot/root ratio of wheat varied with growth temperaturetreatment. The shoot/root ratio of DG wheat was 50% greaterthan WG wheat. In both cereals, nutrient concentrations anddry matter content tended to be greater in organs exposed directlyto low temperatures. The mean specific absorption rates of nutrientswere calculated for the whole period studied for each species/temperaturecombination and were positively correlated with both plant shoot/rootratio and relative growth rate. The data suggest that nutrientuptake rates were influenced primarily by plant demand, withno indication of specific nutrient limitations at low temperatures. Nutrient accumulation, relative growth rate (RGR), rye, Secale cereale cv. Rheidol, temperature, thermal time, Triticum aestivum cv. Mardler, wheat     

Photothermal Time for Flowering in Faba Bean (Vicia faba) and the Analysis of Potential Vernalization Responses

One cultivar and one land-race of faba bean were subjected to18 potentially vernalizing pre-treatments (constant temperaturesof 1, 5 or 9 °C factorially combined with photoperiods of8 or 16 h d^–1 for 10, 30 or 60 d), and then transferredinto four different growing regimes (‘day’/‘night’temperatures of 18/5 °C or 24/13 °C factorially combinedwith photoperiods of 11 or 16 h d–1). Control plants weregrown entirely in the latter four regimes. The times from sowingto appearance of first open flowers were recorded for all plants.Control plants of the land-race Zeidab Local flowered soonerin long days and in the warmer regime. Pre-treatment reducedthe subsequent time to flower in the four growing-on regimesbut most of the variation in the total time to first flowerfor the pre-treated plants was accounted for by differencesin the combined photothermal time accumulated in the two successiveenvironments - which was predicted by a simple photothermalmodel. Thus, there was neither a specific low-temperature nora short-day vernalization response in this accession. Similarly,no true low-temperature or short-day vernalization responsewas detected in the cv. Maris Bead. However, this UK cultivarflowered later than predicted in the 24/13 °C regime, indicatingthat the 24 °C ‘day’ temperature was supraoptimal.Delays to flowering at 24/13 °C were, however, less evidentwhen plants were grown in long days or following prolonged (30–60d) pre-treatments at cool temperatures. Viciafaba faba, bean, flowering, photoperiodism, vernalization, photothermal time, screening germplasm.     

Effects of Temperature and Photoperiod on Phenological Development in Three Genotypes of Bambara Groundnut (Vigna subterranea)

Factorial combinations of four photoperiods (10, 11·33,12·66 and 16 h d^-1) and three mean diurnal temperatures(20·2, 24·1 and 28·1°C) were imposedon nodulated plants of three Nigerian bambara groundnut genotypes[Vigna subterranea (L.) Verdc., syn. Voandzeia subterranea (L.)Thouars] grown in glasshouses in The Netherlands. The photothermalresponse of the onset of flowering and the onset of poddingwere determined. The time from sowing to first flower (f) wasdetermined by noting the day on which the first open flowerappeared. The time from sowing to the onset of podding (p) wasestimated from linear regressions of pod dry weight againsttime from sowing. Developmental rates were derived from thereciprocals of f and p. In two genotypes, 'Ankpa 2' and 'Yola',flowering occurred irrespective of photoperiod and 1/f was controlledby temperature only, occurring sooner at 28·1 than at20·2°C. The third genotype, 'Ankpa 4', was sensitiveto temperature and photoperiod and f was increased by coolertemperatures and photoperiods > 12·66 h d^-1 at 20·2°Cand > 11·33 h d^-1 at 24·1 and 28·1°C.In contrast, p was affected by temperature and photoperiod inall three genotypes. In bambara groundnut photoperiod-sensitivitytherefore increases between the onset of flowering and the onsetof podding. The most photoperiod-sensitive genotype with respectto p was 'Ankpa 4', followed by 'Yola' and 'Ankpa 2'. Therewas also variation in temperature-sensitivity between the genotypesinvestigated. Evaluation of bambara groundnut genotypes foradaptation to different photothermal environments will thereforerequire screening for flowering and podding responses.Copyright1994, 1999 Academic Press Vigna subterranea (L.) Verdc., Voandzeia subterranea (L.) Thouars, bambara groundnut, phenology, photoperiod, daylength, temperature, flowering, podding     

Temperature and photoperiodic control of developmental responses in climatic races of Mimulus

Two strongly differentiated climatic races of the Mimulus cardinalis-lewisiicomplex were grown at a variety of temperatures (3–27°C)and photoperiods (8 and 16 hr) under controlled environmentalconditions. M. cardinalis (the lowland race, 400 m) and M. lewisii(the sub-alpine race, 3200 m) were found to differ in theirphysiological responses to the varied environments in severalsignificant ways: 1) At 27°C (16 hrphotoperiod), M. lewisiisustained 100% mortality in contrast to the substantial growthand flowering of M. cardinalis under these conditions; 2) In8 hr photoperiods at all temperatures, there was little growthand no flowering in M. lewisii whereas there was considerablegrowth at all temperatures, and flowering at 23 and 27°Cin M. cardinalis; 3) At low temperatures (7–15°C),16 hr photoperiods, flowering occurred a week or two earlierin M. lewisii than in M. cardinalis. The lowland race has asignificantly wider temperature and photoperiodic tolerancethan has the sub-alpine race. Applications of gibberellic acidto rosette Mimulus plants under non-inductive conditions (15°C,8 hr photoperiod) promoted vigorous stem elongation withoutflowering. The application of steroids, other hormones and metaboliteshad no observable effects. ¹Present address: Faculty of Botany, Ohio State University,Columbus, Ohio, U.S.A. (Received March 16, 1970; )     

Seed Viability Constants for Lettuce

Seeds of two lettuce cultivars (Lactuca sativa L., cv. Meikoninginand cv. Grand Rapids) were hermetically stored with constantmoisture contents ranging between 3.6 and 17.9 per cent (freshweight basis) at constant temperatures ranging between 5 and75 °C. The decline with time in percentage germination andpercentage normal seedlings was determined for each storagetreatment. The data were fitted to an equation which containsthe constants: K₁, the probit of the initial percentage germinationor normal seedlings; K_E, a species constant; C_W, the constantof a logarithmic moisture term; C_H, the constant of a lineartemperature term and C_Q, the constant of a quadratic temperatureterm. Regression analysis of data from storage periods up to5.5 years at temperatures of 5–75 °C and seed moisturecontents of 3.6–13.6 per cent yielded the following values:K_E= 8.218, C_W=4.797±0.163, C_H=0.0489±0.0050 andC_Q=0.000365±0.000056. Although this equation consistentlyprovided a better fit, simplified equations, assuming eithera log-linear relationship between seed longevity and temperature,or a log-linear relationship between seed longevity and bothmoisture content and temperature, accounted for more than 94per cent of the variation at the restricted temperature rangeof 5–40 °C. Longevity of the same seed lots at sub-zero temperatures (–5,–10 and –20 °C) was studied in separate tests.Freezing damage, resulting in abnormal seedlings in the germinationtest, occurred at –20 °C when the moisture contentof the seeds exceeded 12 per cent. No decline in percentagenormal seedlings was observed after a storage period of 18 monthsor longer at –20 °C, provided the seed moisture contentdid not exceed 9.5 per cent. For seeds stored at –5 and–10 °C with 9.6–12.5 per cent moisture content,the observed rate of decline of percentage normal seedlingswas adequately predicted by the viability equation, using theabove values for the constants. This suggests that for low moisturecontents the viability equation can be applied to estimate longevityat sub-zero temperatures. Lettuce, Lactuca sativa (L.), seed longevity, seed storage, viability constants, storage conditions     

Constant, Fluctuating and Effective Temperature and Seed Longevity: a Tomato (Lycopersicon esculentum Mill.) Exemplar

Tomato seeds with a moisture content of 16.4% were stored hermeticallyat one of five constant temperatures (10, 20, 30, 40, 50 °C)or in one of nine alternating temperature (24 h/24 h) regimes(10/30, 10/40, 10/50, 20/30, 20/40, 20/50, 30/40, 30/50, 40/50°C) for up to 224 d. In each regime, seed survival conformedto cumulative negative normal distributions and all 14 survivalcurves could be constrained to a common origin. Estimates ofthe constants C_Hand C_Qof the viability equation determined atconstant temperatures were 0.0346 (s.e. 0.0058) and 0.000401(s.e. 0.000096), respectively. The effective temperature forseed survival of each alternating temperature regime was alwaysmuch higher than the mean. Tomato seeds were also stored hermeticallyat 15.9% moisture content at 40 °C for 0, 7, 14, 21 or 28d before transfer to 50 °C. This investigation showed thatthe standard deviation of the subsequent survival curves at50 °C was unaffected by the duration of previous storageat 40 °C. The results of both investigations were consistentwith the hypothesis that loss in probit viability is solelya function of the current storage environment, with no effectof change in temperature per se. The application of the viabilityequation to seed survival in fluctuating environments was validatedagainst independent observations for rice in uncontrolled storageconditions. Copyright 2001 Annals of Botany Company Temperature, seed storage, longevity, moisture content, viability equation, tomato, rice     

Photothermal Responses of Flowering in Rice (Oryza sativa)

Durations from sowing to panicle emergence in 16 diverse genotypesof rice (Oryza sativa L.) were recorded in 13 different photothermalregimes, comprising constant and diurnally alternating temperaturesbetween 16 and 32 °C and photoperiods between 10.5 and 15.0h d^–1—all provided by controlled-environment growthcabinets. In 11.5 h days and at sub-optimal temperatures, relationsbetween the rate of progress towards panicle emergence and meantemperature were linear in all genotypes, and amongst thesethe base temperature at that photoperiod varied between 6.6and 11.9 °C. In most cases progress was most rapid at 24–26°C, i.e. the optimum temperature was much cooler than expectedfrom previously published values of times to panicle emergencein a less extensive range of photothermal regimes. Only in threecultivars was it warmer than 28 °C, and in these there weresufficient data to establish that relations between rates ofprogress to panicle emergence and photoperiod in the diurnallyalternating temperature regime of 28–20 °C are alsolinear. Also, the responses of these three cultivars provideno evidence of any interaction between the effects of photoperiodand temperature. We conclude, then, that the model in whichrate of development is a linear function of both temperatureand photoperiod with no interaction, which has been shown tobe common to many other species, also applies to rice. Differencesamong genotypes in relative sensitivity of rate of progresstowards panicle emergence to both temperature and to photoperiodwere considerable; japonica cultivars tended to be more sensitiveto temperature and less sensitive to photoperiod than indicacultivars. Four indica cultivars bred and selected at The InternationalRice Research Institute (IRRI) in the Philippines did not differ(P > 0.10) in their relations between rate of progress towardspanicle emergence and sub-optimal temperatures in a daylengthof 11.5 h, but the optimum temperature for cv. IR 36 was appreciablywarmer than that for the cvs IR 5, IR 8 and IR 42. Oryza sativa, rice, flowering, temperature, photoperiod, photothermal responses     

Restoration of Seed Germination at Supraoptimal Temperatures by Fluridone, an Inhibitor of Abscisic Acid Biosynthesis

Fluridone, an inhibitor of ABA biosynthesis, restored the seedgermination of lettuce (Lactuca sativa L. cv. Grand Rapids)and many other plant species at supra-optimal temperatures.ABA content in lettuce seeds after imbibition quickly decreasedat 23°C, but not at 33°C (a supraoptimal temperature).Fluridone caused a decrease in ABA content at 33°C, whichsuggests that the maintenance of high ABA content could be responsiblefor high-temperature inhibition of germination of lettuce seeds.This probably results from an increase in the rate of ABA biosynthesisat the higher temperature. The present study indicates thatABA plays a decisive role in the regulation of seed germinationat supraoptimal temperatures. ¹ Corresponding author: fax 81-22-717-8834; e-mail yoshi@bios.tohoku.ac.jp