Light and temperature control of germination in Agropyron smithii seeds

In darkness, A. smithii seeds germinated poorly at constanttemperatures but well at alternating temperatures. Prolongedperiods on the high part of the temperature cycles reduced germination;the higher the temperature the shorter was the period requiredon the high part of the temperature cycles for optimum germination.Continuous, unfiltered, incandescent illumination and intermittentfar red at 15?–25?C alternation also inhibited germination;the inhibitory effects were similar to those caused by the highintensity reaction. Far red inhibited germination when appliedafter 1 and 2 complete 15?–25?C cycles in darkness butnot after 3 cycles. Less than 20% of the seeds were under phytochromecontrol at constant 20?C. When red light was applied directlyafter far red that was applied in intermittent cycles at 15?–25?C,however, 50% of the seeds caused to germinate by the alternatingtemperature were shown to be controlled by the reversible phytochromereaction. The induced high-temperature dormancy was overcome by gibberellicacid (GA₃) plus kinetin. The hormonal treatment was much moreeffective than light for breaking dormancy. Inhibition fromprolonged illumination was alleviated or eliminated by GA₃+kinetin.The failure of red light to promote good germination at 20?Cwas also overcome with GA₃+kinetin; effects of light plus thehormone treatments were more than additive. These data suggestthat optimum alternating temperatures facilitate a proper balanceand interaction of hormones, enzymes, substrates and possiblypreexistent P_fr so that the germination of A. smithii seedscan proceed without benefit of a light treatment. (Received July 7, 1976; )     

Contrasted Effects of CO2 on the Regulation of Dormancy and Germination in Xanthium pennsylvanicum and Setaria faberi Seeds

The effects of CO₂ on dormancy and germination were examinedusing seeds of cocklebur (Xanthium pennsylvanicum Wallr.) andgiant foxtail (Setaria faberi Herrm.). The rate of germinationof the giant foxtail seeds as well as cocklebur was promotedby exogenously applied CO₂ at a concentration of 30 mmol mol^-1regardless of the sowing conditions. However, seeds which failedto germinate in the presence of CO₂, entered a secondary phaseof dormancy under unfavourable germination conditions. If CO₂was applied to seeds under conditions such as water stress imposedwith a 200 mol m^-3 mannitol solution, a hypoxic atmosphere of100 mmol mol^-1 O₂ or a treatment of 0·1 mol m^-3 ABA,development of secondary dormancy was accelerated. These contrastedeffects of CO₂ were observed in ecological studies. Under naturalfield conditions germination of buried giant foxtail seeds respondedpositively to CO₂ during a period of release from primary dormancyfrom Feb. to May, but CO₂ accelerated secondary dormancy commencingin early Jun. In other words, in the presence of CO₂, both theenvironmental conditions and the germination states of the seedsclearly showed secondary dormancy-inducing effects. Thus, itseems that CO₂ has contrasted effects on regulation of dormancyand germination of seeds depending on the germination conditions.Copyright1995, 1999 Academic Press Xanthium pennsylvanicum, cocklebur, Setaria faberi, giant foxtail, CO₂, water stress, hypoxia, ABA, germination, secondary dormancy     

Effects of Chilling, Light and Nitrogen-containing Compounds on Germination, Rate of Germination and Seed Imbibition of Clematis vitalba L.

Effects of chilling (5 °C) period, light and applied nitrogen(N) on germination (%), rate of germination (d to 50% of totalgermination; T_50%) and seed imbibition were examined inClematisvitalba L. In the absence of chilling, light and N, germinationwas minimal (3%). When applied alone, both chilling and N increasedgermination. Chilling for 12 weeks increased germination to64%, and 2.5 mM NO^-₃or NH⁺₄increased germination to 10–12%.Light did not increase germination when applied alone, but didwhen applied in combination with chilling and/or N. Half theseed germinated when light was combined with 2.5 mM NO^-₃or NH⁺₄.The influence of chilling, light and/or N on germination wasgreater when combined, than when either factor was applied alone.Both oxidized (NO^-₃) and reduced (NH⁺₄) forms of N increasedgermination, but non-N-containing compounds did not, suggestingthe response was due to N and not ionic or osmotic effects. Without additional N, T_50%decreased from 16–20 d at zerochilling, to around 5 d at 8 and 12 weeks chilling. AlthoughT_50%was not influenced by an increase in NO^-₃or NH⁺₄from 0.5to 5.0 mM , it did increase with additional applied N thereafter.However, the magnitude of the N effect was small compared tothat of chilling. Like germination, seed imbibition increasedwith a longer chilling period, but in contrast imbibition decreasedslightly with increased applied NO^-₃or NH⁺₄. It is argued thatincreased imbibition is not directly related to an increasein total germination, but that it may be related to the rateof germination. Possible mechanisms involved in the reductionin dormancy ofC. vitalba seed are discussed. Clematis vitalba L.; germination; dormancy; imbibition; rate of germination; chilling; light; nitrate; ammonium; nitrogen; phytochrome     

Germination of Leymus arenarius and its Significance for Land Reclamation in Iceland

Leymus arenarius is used to stabilize the extensive areas oferoded volcanic sand in Iceland, both inland and on the coast.It has been reported previously to produce seeds of generallylow viability. We investigated the potential for seed dormancyand the responses of germination to temperature, light and salinity,as part of a re-assessment aimed at improving reclamation procedures. Contrary to previous reports, high rates of germination couldbe obtained under certain conditions. All caryopses were soakedin water (24 h) and stratified for 2 weeks (5 °C) beforethe subsequent germination tests. Constant temperatures or exposureto light resulted in very poor germination. Close to 100% germinationcould be obtained within 2 weeks in continuous darkness, underalternating temperatures with an amplitude of 10-20 °C ona 12 h cycle; high day temperatures appear to be important.Diurnal fluctuations in temperature of this order occurred underaverage weather conditions in the black, volcanic sands in Icelandduring the growing season (May-Sep.). The dark requirement isinterpreted as a selective response to the adverse conditionsfor establishment at the surface of the sand; the alternatingtemperature requirement may be a response to ensure dormancyunder deep burial with accreting sand, although it could havea role in gap-sensing under established canopies. Scarification,surface sterilization and treatment with n -butanol or KNO₃were all generally ineffective in promoting germination. Nearlyall caryopses that did not germinate, in all treatments, remainedviable. Caryopses of coastal populations of Leymus arenarius showedsignificantly higher total germination and more rapid germinationin 100 mmol l^-1 and 300 mmol l^-1 NaCl solutions than inlandpopulations. The inhibition of germination by salinity was anosmotically enforced dormancy effect rather than a lethal, toxicone; caryopses that had not germinated in saline solution generallywere able to germinate subsequently, when transferred to non-salineconditions.Copyright 1994, 1999 Academic Press Germination, Leymus arenarius (lymegrass), Triticeae, survival analysis, fluctuating temperature, sand stabilization, salinity tolerance, Iceland     

Germination of seeds in Jussiaea suffruticosa

Seeds of Jussiaea suffruticosa reach high germination percentagesonly when exposed to long periods of continuous illumination.The light reaction may be repeatedly reversed by short exposuresto red and far red light, thus being mediated by the phytochromesystem. Seeds also germinate at high percentages if exposedto various cycles of 1 hr light and 24 hr of darkness at 20°C.If the temperature in the periods of darkness is raised up to30°C or lowered to 10°C the promotive effect of lightis inhibited. High temperatures (35°C) during imbibitionhave a promotive effect, whereas a pure O₂ atmosphere decreasesthe response to light. KNO₃ and kinetin enhance the responseto light but do not provoke germination in the dark. Only ifseed coats are punctured or removed does germination in thedark occur. (Received January 14, 1969; )     

Low‐molecular weight carbohydrates modulate dormancy and are required for post‐germination growth in turions of Spirodela polyrhiza

The aquatic duckweed Spirodela polyrhiza propagates itself vegetatively by forming turions – bud‐like perennation organs – in the autumn, which spend the winter on the bottom of ponds and then germinate in the following spring and proliferate on the water surface. Newly formed turions usually require a period of cold after‐ripening and light to germinate effectively, but an ample supply of exogenous sugar can lead to germination even in the dark and independent of after‐ripening. The results of the present study indicate that the availability of readily metabolised carbohydrates is a determining factor for turion germination. Freshly harvested turions do not contain soluble, low‐molecular weight carbohydrates at a level sufficient to allow germination to take place, but after‐ripened turions do. Augmentation of the soluble carbohydrate content during after‐ripening derives from gradual breakdown of reserve starch of the turions. The long time required for any germination to be observed in turions incubated in darkness and the limited frequency of germination in the dark (about 50% of turion population), even with an ample external sugar, supply emphasise that both after‐ripening and light are essential for ensuring rapid germination and subsequent frond proliferation at an ecologically appropriate time. The carbohydrate supply required for rapid proliferation of the fronds produced at germination is provided by the rapid light‐induced breakdown of turion reserve starch.     

Ethylene, Nitrate and Nitrite Interactions in the Promotion of Dark Germination of Common Purslane Seeds

Ethylene (10 µ1^–1) caused about one-third of highlydark-dormant seeds of common purslane (Portulaca oleracea L.)to germinate in the dark. Attempts were made to increase germinationin the dark with nitrate and ethylene combinations. When applieddirectly to the seeds, KNO₃ did not stimulate germination andKNO₃ plus ethylene did not increase germination above that ofethylene alone. Pre-incubation of seeds in KNO₃ for 4 to 7 dbefore the ethylene applications significantly increased germination.The effects of the KNO₃ pre-incubation were additive at eachof four ethylene concentrations (0.1–100 µ11^–1).Potassium nitrate was effective only when ethylene followedthe KNO₃ pre-incubation period. Potassium nitrite stimulatedabout 25 per cent of the seeds to germinate without a pre-incubationperiod and without ethylene. Also, ethylene plus KNO₂ enhancedgermination above that achieved by either stimulus alone. Silvernitrate did not block the ethylene promotion of germination,but reversed the typical ethylene inhibition of seedling growthfollowing germination. The results support the views that nitrateexerted its effect via conversion to nitrite within the seedand that the rate of nitrate conversion may be a limiting factorin the dark germination of common purslane seeds. Ethylene mayfacilitate nitrite activity by increasing seed sensitivity tothe stimulus. Common purslane, Portulaca oleracea L., ethylene, nitrate, nitrite, germination, dormancy     

Glaucium flavum Seed Germination - an Ecophysiological Approach

The yellow horned-poppy Glaucium flavum Crantz shows a finaldark germination which is of characteristically ‘mediterranean’type (maximal response at the temperature range 5–15 °C),though a considerable broadening is brought about, both by ared light pulse and a stratification treatment. Seeds imbibedin darkness at 25 °C for even a few hours are induced todevelop a secondary dormancy (thermodormancy) which can be releasedby light and stratification. The well known time dependenceof light sensitivity and the gradually imposed induction oflight indifference at supraoptimal temperatures have also beenshown. Seeds imbibed under regimes simulating those met naturallyin Greece during November or April, do not germinate when illuminatedwith white light (     

Factors regulating germination of resting cysts of the spring bloom dinoflagellate Scrippsiella hangoei from the northern Baltic Sea

The role of cyst germination as a factor in bloom initiationwas investigated for the dinoflagellate Scrippsiella hangoei(Schiller) Larsen from the northern Baltic Sea. This speciesblooms in very cold, often ice-covered waters, and is responsiblefor a significant fraction of the production in that region.Dormancy, temperature, oxygen and light were studied as factorspotentially controlling the germination of S.hangoei restingcysts. Laboratory-stored and field-collected cysts began togerminate in December following a mandatory dormancy periodlasting 6 months. Germination after this maturation intervalwas maximal when temperatures were within a 0–9°C‘window’. Mandatory dormancy is therefore the primaryfactor regulating the timing of germination in this species,as temperatures in the natural environment normally fall withinthis range at the time when S.hangoei cysts deposited the precedingyear have matured. Non-optimal temperatures, darkness and lowoxygen conditions all maintain a state of quiescence in thecysts. Cysts could germinate in darkness, but the rate of excystmentwas significantly higher in the light. Likewise, excystmentwas completely inhibited in anoxic conditions and was reducedunder severe hypoxia, with normal germination under moderatehypoxic concentrations. Temporary exposure to high sulfide concentrationspermanently reduced germination potential, indicating that S.hangoeicysts have low resistance to oxygen deficiency. Prolonged periodsof anoxia at the sediment surface, as frequently occurs in thestudy area, might reduce the size of the viable cyst pool andthus, alter the magnitude of the inoculum for S.hangoei bloominitiation. Together, these internal and external regulatoryfactors play important roles in the bloom dynamics of this importantdinoflagellate.     

Metabolism of Glycollate by Lemna minor L. Grown on Nitrate or Ammonium as Nitrogen Source

Marques, I. A., Oberholzer, M. J. and Erismann, K. H. 1985.Metabolism of glycollate by Lemna minor L. grown on nitrateor ammonium as nitrogen source.—J. exp. Bot. 36: 1685–1697. Duckweed, Lemna minor L., grown on inorganic nutrient solutionscontaining either NH₄⁺ or NO₃^– as nitrogen source wasallowed to assimilate [1-¹⁴C]- or [2-¹⁴C]glycollate during a20 min period in darkness or in light. The incorporation ofradioactivity into water-soluble metabolites, the insolublefraction, and into the CO₂ released was measured. In additionthe extractable activity of phosphoenolpyruvate carboxylasewas determined. During the metabolism of [2-¹⁴C]glycollate in darkness, as wellas in the light, NH₄⁺ grown plants evolved more ¹⁴CO₂ than NO₃^–grown plants. Formate was labelled only from [2-¹⁴C]glycollateand in NH₄⁺ grown plants it was significantly less labelledin light than in darkness. In NO₃^– grown plants formateshowed similar radioactivity after dark and light labelling.The radioactivity in glycine was little influenced by the nitrogensource. Amounts of radioactivity in serine implied that thefurther metabolism of serine was reduced in darkness comparedwith its metabolism in the light under both nitrogen regimes.In illuminated NH₄⁺ plants, serine was labelled through a pathwaystarting from phosphoglycerate. After [1-¹⁴C]glycollate feedingNH₄⁺ grown plants contained markedly more radioactive aspartateand malate than NO₃^– plants indicating a stimulated phosphoenolpyruvatecarboxylation in plants grown on NH₄⁺. Key words: Photorespiration, glycollate, nitrogen, Lemna     

Photophysiology of turion formation and germination inSpirodela polyrhiza

Standardized laboratory techniques for the vegetative growth of the duckweedSpirodela polyrhiza (Lemnaceaé), and for formation as well as germination of their turions were described. Increasing photon fluence rates of blue or red light increased the yield of turions. A specific stimulating effect of blue light was demonstrated under autotrophic but not under mixotrophic conditions. Therefore the spectral composition of light is not important in mixotrophic formation of turions whereas in autotrophic formation light sources with a higher portion of blue light are recommended. Dark-grown (etiolated) turions showed accelerated germination and higher germination percentage in comparison with light-grown turions after induction by a single red light pulse. This difference was overcome in continuous red light by speeding up the germination response of light-grown turions. Use of Petri dishes (8 cm³ nutrient solution) instead of Erlenmeyer flasks (50 cm³ nutrient solution) retarded germination response. Especially for long term experiments the use of Erlenmeyer flasks is recommended. Storage of turions for 72 h at 25 ‡C following at 5 ‡C in darkness after-ripening resulted in a decreased lag phase of the light-induced germination both after induction by a single light pulse and in continuous light. We thank Dr. Halina Gabrys, University of Crakow, Poland for critical discussion.     

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.     

Rate of Change in Dormancy Level and Light Requirement in Weed Seeds During Stratification

The rate of change in dormancy level and light requirement,induced during stratification at 3.2 °C, was investigatedin seeds ofStellaria media, Cerastium fontanum, Veronica agrestisandTaraxacumofficinale.Two stratification environments, soil and wet filterpaper in petri-dishes, were used. On nine occasions during a6 week stratification period, germination was tested under threelight conditions at 3.5/18.5 °C: (1) darkness; (2) light;and (3) short-term light exposure followed by darkness. Priorto stratification, germination in all species was 89% in lightand 53% in darkness. Within 2 weeks of stratification, germinabilityinV. agrestisandS. mediaseeds decreased in all treatments. InC.fontanumandT. officinaleseeds, germinability also decreasedafter 2 weeks but only in the dark treatment, indicating inductionof a light requirement. After two more weeks of stratification,the induced dormancy inS. mediaseeds stratified in soil becameweaker and the light requirement inT. officinaleseeds was lost.Differences between the two stratification environments and/orinteractions between light conditions, stratification environmentsand time were found for all species. These results suggest that:(1) the dormancy level and the light requirement of seeds maychange dramatically over relatively short-time periods duringstratification; and (2) germinability depends on the stratificationenvironment experienced by the seeds. Predicting the dormancylevel or light requirement in a seed batch is difficult andrequires a thorough knowledge of the effect of the stratificationconditions used.Copyright 1997 Annals of Botany Company Burial; Cerastium fontanumBaumg.; chickweed; cold stratification; common mouse-ear; dandelion; dormancy; light requirement; seed; Stellaria media(L.) Vill.; speedwell; Taraxacum officinalegroup; Veronica agrestisL.; weed     

A Model of the Effects of a Wide Range of Constant and Alternating Temperatures on Seed Germination of FourOrobanche Species

Seeds of the obligate parasitic plants, Orobanche spp., wereconditioned in water or GA₃for 2 or 12 weeks and then stimulatedto germinate by the synthetic stimulant GR24. Temperature treatmentsduring the germination tests comprised 169 different constantand alternating temperature regimes on a two-dimensional gradientplate. Optimum temperatures for germination of seeds of O. aegyptiacaand O. crenata were 18–21 °C and 18 °C, respectively.However, longer conditioning periods slightly lowered the optimain both species, and the maximum germination percentage wasalso reduced due to an induction of secondary dormancy. At agiven mean temperature, more seeds germinated at constant thanat alternating temperatures. Results were analysed in termsof characteristics of alternating temperatures that appearedto control germination, i.e. mean temperature, maximum temperature,amplitude (difference between daily maximum and minimum temperatures)and thermoperiod (the time spent at the maximum temperatureeach day). Final germination was modelled on the basis of therebeing two prerequisites for germination: a minimum mean temperaturewhich must be exceeded and a maximum temperature above whichthe seed will not germinate. These two requirements were assumedto be independent and to be normally distributed in the seedpopulation so that final germination could be described by amultiplicative probability model. Because of the response tomaximum temperature, inhibitory effects were more evident atalternating temperatures. Amplitude and thermoperiod influencedthis effect of maximum temperature. The implications of thedetrimental effect of alternating temperatures for germinationofOrobanche spp. in the field are discussed. Copyright 1999Annals of Botany Company Orobanche aegyptiaca, O. crenata, O. cernua, O. minor, broomrape, seed germination, temperature, germination model, secondary dormancy.     

Induction of Secondary Dormancy in Chenopodium bonus-henricus L. Seeds by Osmotic and High Temperature Treatments and Its Prevention by Light and Growth Regulators

Factors controlling the establishment and removal of secondary dormancy in Chenopodium bonus-henricus L. seeds were investigated. Unchilled seeds required light for germination. A moist-chilling treatment at 4 C for 28 to 30 days removed this primary dormancy. Chilled seeds now germinated in the dark. When chilled seeds were held in the dark in −8.6 bars polyethylene glycol 6000 solution at 15 C or in water at 29 C a secondary dormancy was induced which increased progressively with time as determined by subsequent germination. These seeds now failed to germinate under the condition (darkness) which previously allowed their germination. Continuous light or daily brief red light irradiations during prolonged imbibition in polyethylene glycol solution at 15 C or in water at 29 C prevented the establishment of the secondary dormancy and caused an advancement of subsequent germination. Far red irradiations immediately following red irradiation reestablished the secondary dormancy indicating phytochrome participation in “pregerminative” processes. The growth regulator combination, kinetin + ethephon + gibberellin A₄+A₇ (GA₄₊₇), and to a relatively lesser extent GA₄₊₇, was effective in preventing the establishment of the secondary dormancy and in advancing the germination or emergence time. Following the establishment of the secondary dormancy by osmotic or high temperature treatments the regulator combination was relatively more active than light or GA₄₊₇ in removing the dormancy. Prolonged dark treatment at 29 C seemed to induce changes that were partially independent of light or GA₄₊₇ control. The data presented here indicate that changes during germination preventing dark treatment determine whether the seed will germinate, show an advancement effect, or will become secondarily dormant. These changes appear to be modulated by light and hormones.     

Diurnal regulation of NO-3 uptake in soybean plants IV. Dependence on current photosynthesis and sugar availability to the roots

The short-term dependence of NO^–₃ uptake upon photosynthesisand sugar supply to the roots of soybean plants was investigatedin a series of experiments where CO₂ availability, light intensityor conduction of phloem sap to the roots were severely limited.Removal of CO₂ from the atmosphere or girdling of the stem equallyprevented the stimulation of NO^–₃ uptake when plants weretransferred from darkness to the light. The effect of thesetwo treatments can be reversed by CO₂ re-supply or by additionof 10 mM glucose in the nutrient solution, respectively. Glucosewas also more effective in stimulating NO^–₃ uptake byintact plants in darkness than in light. Collectively, theseobservations are interpreted as evidence that the diurnal changesin NO^–₃ uptake are due to decreased phloem transport ofphotosynthates in darkness. Accordingly, the magnitude of thesechanges was much dependent on starch accumulation in the leavesat the end of the photo-period. Shading the plants lowered thisaccumulation, and resulted in an amplification of the diurnalchanges in NO^–₃ uptake. These results are discussed inconnection with the hypothesis that the carbon-dependent plasticityof the night/day ratio of NO^–₃ uptake is an importantfeature of the co-ordination of the acquisition of N and C bythe plant. Key words: Glycine max, light/dark cycle, NO^–₃ uptake, C and N acquisition     

Recovery of Germination from Different Osmotic Conditions by Four Halophytes from Southeastern Spain

Seeds of four halophytes from southeastern Spain (the perennialsHalocnemum strobilaceum,Arthrocnemum macrostachyum and Sarcocorniafruticosa, and the annual Salicornia ramosissima) were exposedto iso-osmotic stress with NaCl, MgCl₂, MgSO₄and Na₂SO₄. Theosmotic potential that enforced dormancy in the majority ofseeds was determined. The percentage of ungerminated seeds thatrecovered when they were transferred to distilled water didnot differ significantly from the percentage germination ofseeds in distilled water controls, irrespective of the saltused to impose the stress. Therefore, the factor responsiblefor the dormancy of seeds seems to be the decrease in osmoticpotential. Such osmotic pretreatments promoted an increase inthe rate of recovery germination which, inArthrocnemum macrostachyumand Sarcocornia fruticosa, doubled their rates of germinationcompared to distilled water controls. The osmotic potentialsof the soils where the four species occur naturally were morenegative than those allowing seeds to germinate after osmoticstress. Copyright 2000 Annals of Botany Company Arthrocnemum macrostachyum, Halocnemum strobilaceum, halophytes, osmotic stimulation, recovery of seed germination, Salicornia ramosissima, Sarcocornia fruticosa.     

Germination and Dormancy in Immature and Fresh-mature Lettuce Seeds

The effects of red light, far-red light, Gibberellin A₃, andethephon were studied on the germination of lettuce seeds cv.Grand Rapids harvested at different stages of development. Seeds did not become capable of germination until 8 days afteranthesis. Red light promoted seed germination from the age of8–9 days following anthesis up to the newly mature stage.Ten or 11 days following anthesis, a large percentage of seedsbecame capable of germination in the dark and therefore couldbe considered not dormant. They were affected by far-red light,but less so than the mature seeds. The effect of light on the germination of developing seeds appearedto be similar to the known light effect on mature lettuce seedgermination. Gibberellin A₃ and ethephon had no effect on immatureand fresh seed germination. Lactuca sativa L., Lettuce, germination, dormancy, red light, far-red light, gibberellin A₃, ethephon     

Ethylene Release from Leaves of Xanthium strumarium L. and Zea mays L.

The release of ethylene into sealed Erlenmeyer flasks by intactleaves and leaf discs of Xanthium strumarium L. a C₃ plant andZea mays L. a C₄ plant were compared both in white light andin darkness. The effects of the presence or absence of addedCO₂ (in the form of sodium bicarbonate) the photosynthetic inhibitor3-[3,4-dichlorophenyl]-l, l-dimethyl urea (DCMU) and 1-aminocyclopropane-1-carboxylicacid (ACC), the precursor of ethylene in higher plants, werealso investigated. The rate of ethylene release from leaf tissue of Xanthium inthe absence of added CO₂ was markedly reduced in the light (i.e.at the CO₂ compensation point). Treatments that would enhancethe CO₂ availability to the tissue (i.e. added bicarbonate,darkness, treatment with DCMU) allowed higher levels of ethylenerelease. Incubation of the tissue with ACC considerably enhancedthe release of ethylene compared to that from the correspondingcontrol tissue without ACC. However, the pattern of ethylenerelease induced by the various treatments was similar with orwithout added ACC. When tissue, in the absence of added CO₂, was transferred fromlight to darkness, and back to light for 90 min periods, theethylene release rates Increased during the interposed darkperiod but resumed the lower rate during the final light period.The addition of CO₂ in the light resulted in a similar rateof ethylene release to that found in the dark. The overall pattern of ethylene release from Zea leaf tissuesubjected to light and dark in the presence or absence of addedCO₂ was similar to that of Xanthium. However, two or three timesmore ethylene was released from maize leaves in the light whenCO² was added compared to that generated in the dark. This isin marked contrast to Xanthium, where, under the light conditionsused, the ethylene release rate in the dark equalled or exceededthat occurring in the light, even in the presence of high levelsof CO₂. A very low rate of ethylene release was observed atthe CO₂ compensation point of maize. A speculative model is presented to explain how photosyntheticactivity might act as a key factor in regulating ethylene evolutionfrom leaf tissue in these experiments. It invokes the conceptof an inhibition by CO₂ of ethylene retention or breakdown thuspermitting more ethylene to be released from the leaves.     

Diurnal regulation of NO3- uptake in soybean plants III. Implication of the Dijkshoorn-Ben Zioni model in relation with the diurnal changes in NO3- assimilation

According to the Dijkshoorn-Ben Zioni model, NO₃^– uptakein the roots is stimulated by NO₃^– assimilation in theshoots, through downward phloem transport of malate synthesizedin response to reduction of NO₂^– to NH³. In this paper,one hypothesis resulting from this model was tested, i.e. thatthe diurnal changes in NO₃^– uptake are due to the lightdependence of NO₃^– reduction in the leaves. This dependencewas studied in detached leaves transferred to deionized wateror supplied via the transpiration stream with similar amountsof ¹⁵NO₃^– in light or darkness. In the dark, the reductionof previously stored NO₃^– or xylem-borne ¹⁵NO₃^–was generally about 40–50% of that measured in the light.Glucose supply to the detached leaves stimulated NO₃^–reduction in the dark, but not enough to increase it up to thesame rate as in the light. Nitrite reduction in detached leaveswas much less affected by darkness, and could be maintainedat a high level by exogenous supply of substrate. Advantagewas taken from this last observation to sustain NO₂^–reductionin attached darkened shoots at the same rate as in the light,by ensuring an appropriate delivery of NO₂^– from the xylem.Although this was assumed to restore the light level of theassociated synthesis of malate, it led to a marked inhibitionof NO₃^– uptake. In addition, the direct supply of malateto the shoots or to the roots failed to prevent the decreaseof NO₃^– uptake in darkness. Thus, our conclusion is thatthe mechanisms evoked in the Dijkshoorn-Ben Zioni model do notplay an important role in the diurnal variations of NO₃^–uptake in soybean plants. Key words: Glycine max, light/dark cycle, malate synthesis, NO₃^– reduction, NO₃^– uptake