Starch Synthesis During Dormancy Breakage in Oilseed of Corylus avellana

Dormancy in seed of Corylus avellana L. (hazel) is broken bya sustained period of cold stratification. During this timeboth cytological and metabolic changes occur. Starch was presentinitially at a low level but increased by 20% in the embryonicaxes of hazel seeds during stratification at 5 °C, whileit decreased rapidly and then remained constant in the embryonicaxes from seeds held at 20 °C. Histochemical study confirmedthis analytical result. A comparison of the developmental patternof starch level with bound and soluble ADP glucose-starch synthaseactivity at 5 and 20 °C showed that the accumulation ofstarch in the embryonic axes followed an enhanced activity ofthe granule-bound ADP glucose-starch synthase. Cold stratificationresulted in an increase in starch content, which was probablyas a result of gluconeogenesis from products of reserve lipidhydrolysis. Corylus avellana L., hazel, starch, ADP glucose-starch synthase, stratification     

A Comparison of Petiolar Growth of Isolated Hazel Cotyledons in Response to Stratification and Exogenous GA3

Following stratification seeds of Corylus avellana exhibitedtheir characteristic ability to germinate at 20 °C undermoist conditions. Stratification of the intact fruit also stimulatedelongation of the cotyledonary petiole when isolated cotyledonswere transferred to moist conditions at 20 °C. GA₃ inducedboth of these effects in non-stratified material. ABA substantiallydecreased seed germination and the response of cotyledonarypetioles to stratification and GA₃. CCC² applied to stratifiedor GA₃-pretreated cotyledons did not depress the final percentageof growing petioles. Cotyledons can clearly regulate the development of their petiolesin the absence of the embryonic axis. It is concluded that thereis at least one gibberellin-sensitive site in the cotyledonscapable of initiating petiole development independent of axiscontrol.     

Biochemical Changes in Seed of Pinus radiata D. Don during Stratification

Stratification at 0 °C accelerates subsequent germinationof seed of Pinus radiata D. Don when transferred to 25 °C;the effect of low temperature is on the megagametophyte, notthe embryo. Organic acids, sucrose, and organic phosphates accumulatein the seed during stratification but lipase and invertase havelow activities which do not increase during treatment at 0 °C.We conclude that this accumulation of metabolites underliesthe increase in rate of germination of stratified seed. Treatingseeds at 0 °C rather than 5 °C separates effects dueto stratification and growth.     

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.     

RNA Metabolism During Breakage of Seed Dormancy by Low Temperature Treatment of Fruits of Acer plataanoides(Norway Maple)

Stratification of Acer platanoides fruits at 4 °C led toan accumulation of RNA in the embryo axis and to breakage ofseed dormancy. The accumulated RNA was mainly rRNA. Storageof fruits at 17 °C led neither to an accumulation of RNAnor to breakage of dormancy. The proportion of embryo axis mRNA,as measured by poly(A) content, decreased during both fruitstorage and stratification, although levels of poly(A) wereconsistently lower in embryo axes from stored seeds. Isolatedembryos from both stored and stratified fruits were capableof incorporating [³H]uridine into embryo axis RNA. When assayedat 17–20 °C, however, this incorporation was significantlylower in embryos of stored fruits. The distribution of radioactivitybetween the different RNA species was similar in both storedand statified seeds. Acer platanoides, Norway Maple, dormancy, fruit, seed, ribonucleic acid, stratification, nucleic acid metabolism     

Field Measurements of the Gas Exchange of Woody Plant Species in Simulated Sunflecks

The photosynthetic responses of eight tree and shrub speciesto simulated sunflecks was measured in the field. The net carbonexchange (NCE) of Corylus avellana and Ulmus glabra increasedwith irradiance up to the maximum irradiance of 230 µmolm^–2 s^–1. The NCE of Fraxinux excelsior, Hedera helixand the sun and shade forms of Rhododendron ponticum saturatedat about 120 µmol m^–2 s^–1 whereas the NCEof Ilex aquifolium, Daphne laureola and Fagus sylvatica hadeffectively saturated at 27 µmol m^–2 s^–1. In all cases the quantum efficiency of NCE could be predictedfrom measurements of chlorophyll fluorescence and the maximumvalue for NCE from measurements of stomatal conductance. Therelationships were combined into a model for predicting NCE/irradiancecharacteristics. Corylus avellana L., Daphne laureola L., Fagus sylvatica L., Fraxinus excelsior L., Hedera helix L., Ilex aquifolium L., Prunus laurocerasus L., Rhododendron ponticum L., Ulmus glabra Huds., gas exchange, stomatal resistance, water use efficiency, chlorophyll fluorescence, quantum efficiency     

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     

Pentose phosphate metabolism during dormancy breakage in Corylus avellana L.

Commercially obtained fruits of Corylus avellana exhibit the characteristic loss of dormancy of this seed following chilling under moist conditions. The activities of cytosolic and organellar enzymes of pentose phosphate pathway in cotyledonary tissue were assayed throughout stratification and over a similar period in damp vermiculite at 20° C. Glucose-6-phosphate dehydrogenase (G6PDH) and 6-phosphogluconic acid dehydrogenase (6PGDH) were both found in cytosolic extracts in all treatments; only 6PGDH was present in the organellar fraction.The enzyme activities monitored in seeds at 20° C remained relatively constant over the course of the investigation except in the case of cytosolic 6PGDH where it is suggested an inhibitor of the enzyme accumulated. This inhibitor was removed by the partial purification procedure. Increases in the activities of the enzymes occurred during stratification, the major increase coinciding exactly with dormancy breakage but prior to the initiation of germination. The marked increase in G6PDH and 6PGDH concurrent with the change in germination potential of the chilled seed may have considerable biochemical significance in breaking down the dormant state.Abbreviations G6P glucose-6-phosphate - G6PDH glucose-6 phosphate dehydrogenase - NADP nicotinamide adenine dinucleotide phosphate - 6 PGDH 6-phosphogluconic acid dehydrogenase - PPP pentose phosphate pathway     

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     

Low Temperature Storage of Caryopses of Triticum durum: Viability and Longevity

Germination of Triticum durum Desf. ‘Cappelli’ caryopsesstored in hermetically-sealed containers at 10°C or -20°Cwas analysed. Caryopses were maintained in laboratory conditions(20 ± 4°C) prior to controlled storage, which began5 d, 240 d and 7 years after harvesting. In addition, after9 years of storage, one 10°C stored batch of caryopses andtwo -20°C stored batches were returned to laboratory conditions.Germination over time and seed longevity were investigated.Results showed that: (1) under laboratory conditions, caryopsesin relative (primary) dormancy at the beginning of storage hadlost dormancy after 45 d and germination ability was lost bythe end of year 7. (2) When stored at 10°C, relative dormancyin caryopses was lost within 1 year, but 100% germination abilitywas retained after 23 years of storage. (3) When stored at -20°C,caryopses that were dormant at the beginning of storage (5 dafter harvesting) maintained this condition for 23 years whilecaryopses which were placed in storage 240 d after harvesting,when relative dormancy had already been broken, maintained 100%germination ability. Caryopses returned to laboratory conditionsafter 9 years of storage at 10°C or -20°C showed thesame trend as caryopses maintained exclusively in laboratoryconditions since the time of harvesting. Caryopses removed from-20°C overcame relative dormancy in 50 d and maintainedgermination ability for roughly 7 years, while those removedfrom 10°C lost the ability to germinate by the end of thefifth year. Copyright 2000 Annals of Botany Company Germination, longevity, low-temperature-storage, Triticum durum, viability     

Light-Sensitivity of Hazel Seeds with Respect to the Breaking of Dormancy

Light breaks the dormancy of hazel (Corylus avellana L.) seedswhen the testa is removed. Light, acting via phytochrome, alsopromotes the germination of hazel seeds when the embryonic axisis surgically uncovered. In such seeds with the axis uncoveredremoval of the testa is antagonistic to the light promotionof germination. (Received January 17, 1982; Accepted April 25, 1983)     

Nuclear Replication Activity During Seed Development, Dormancy Breakage and Germination in Three Tree Species: Norway Maple (Acer platanoidesL.), Sycamore (Acer pseudoplatanusL.) and Cherry (Prunus aviumL.)

Flow cytometric analyses of nuclear DNA levels were carriedout during development, stratification and germination of dormantseeds from three tree species with contrasting characteristics.Norway maple (Acer platanoides) and sycamore (Acer pseudoplatanus)have orthodox (desiccation-tolerant) and recalcitrant (desiccation-sensitive)storage behaviours, respectively, and require only a periodof cold to break dormancy, whereas, orthodox cherry (Prunusavium) seeds require an initial warm period before cold stratificationto fully stimulate germination. Whole embryos and radicle tipsof both Norway maple and sycamore were found to have stablehigh levels of 4C DNA during the latter stages of developmentand both contained nuclei arrested at the 2C and 4C levels atmaturity. Mature cherry embryos had nuclei predominantly arrestedat the 2C level. This suggests that the acquisition of desiccationtolerance is not correlated with the arrest of the cell cycleat any particular nuclear DNA level. Neither DNA replicationin radicle cells nor germination occurred when seeds were maintainedmoist at a constant 20 °C. However, in the late stages ofcold treatment during stratification, nuclear DNA levels inradicle cells changed in advance of radicle emergence in theorthodox Norway maple and cherry, whereas in the recalcitrantsycamore, change was not recorded until after radicle emergence.These results show that DNA replication has potential use asan indicator of the progress of tree seeds through stratificationtreatments used to break some types of dormancy. The ways inwhich this indicator could be exploited for seed quality andperformance testing are discussed.Copyright 1998 Annals of BotanyCompany Norway maple,Acer platanoidesL., sycamore,Acer pseudoplatanusL., cherry,Prunus aviumL., DNA replication, flow cytometry, seed dormancy, stratification     

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 (     

Modelling Temperature Effects in Breaking Rest in Red-osier Dogwood (Cornus sericea L.)

Temperature requirements for bud development after a rest period(breaking rest) from maximum rest to end of rest were determinedto develop an empirical model for predicting rest developmentin terminal vegetative buds of red-osier dogwood (Cornus sericeaL.). One-year-old plants at maximum rest were exposed to temperaturesfrom 5 to 20 °C a 12 h photoperiod (SD) in growth chambers.Depth of rest was measured by days to bud break in either 16h photoperiod (LD) or natural daylength at 20/15 °C/nighttemperature. Developmental stages during rest development wereexpressed by degree growth stage (°GS). Chilling was effective breaking rest after plants attained maximumrest (270 °GS). Development during rest (breaking rest)increased with decreasing temperature. No significant developmentoccurred at 20 °C. Rate of rest development (°GS h^–1)at all temperatures varied during the breaking rest period anddepended on developmental stage (°GS). A °GS model describedand quantified rest development (°GS). Using temperatureand developmental stage, the model predicted end of rest (315°GS)within 3 days and daily rest development (°GS) in both years. Cornus sericea L, Cornus stolonifera Michx, dogwood, bud development, dormancy, temperature effects, chilling, degree growth stage     

Dormancy in Rice Seed: IV. VARIETAL RESPONSES TO STORAGE AND GERMINATION TEMPERATURES

Serial germination tests were carried out on dormant seeds ofsix rice varieties (four varieties of Oryza sativa L. and twovarieties of O. glaberrima Steud.) stored at several differentconstant temperatures within the range 27° C to 57°C. Probit analyses of the results were carried out to determmethe mean dormancy period for each variety at each temperature.Regression lines fitted to these data showed that there is adirect negative relationship between storage temperature andlog mean dormancy period over the range 27° C to 47°C, thus confirming a previous result obtained on a single variety.At 7° C there were indications of a slight departure fromthis relationship in that the mean dormancy periods at thistemperature were slightly longer than would have been predictedby extrapolation of the regressions calculated from the resultsobtained at lower temperatures. In all cases where the resultswere unambiguous (i.e. in all the sativa varieties and one ofthe glaberrima varieties) a constant Q₁₀ of 3.13 was shown forthe rate of loss of dormancy over the range of storage temperaturesfrom 27° C to 47° C. In the remaining glaberrima variety,where the results were less reliable, a Q₁₀ of 2.54 was found. Germination tests on all varieties were carried out at 32°C, but in the case of one sativa variety germination tests forall storage treatments were also duplicated at 27° C. Thisinvestigation showed that, in contrast to the effect of storagetemperature, the higher temperature during the germination testconsistently resulted in a lower percentage germination. Inaddition the results demonstrated that there is no interactionbetween storage temperature and germination temperature: consequentlythe storage-temperature coefficient has the same value irrespectiveof germination temperature. Some theoretical implications ofthe results are discussed.     

Water Relations of Seed Development and Germination in Muskmelon (Cucumis melo L.): VII. INFLUENCE OF AFTER-RIPENING AND AGEING ON GERMINATION RESPONSES TO TEMPERATURE AND WATER POTENTIAL

The effects of storage conditions on the germination of developingmuskmelon (Cucumis melo L.) seeds were tested to determine whetherafter-ripening is required to obtain maximum seed vigour. Seedswere harvested at 5 d intervals from 35 (immature) to 60 (fullymature) days after anthesis (DAA), washed, dried, and storedat water contents of 3·3 to 19% (dry weight basis) at6, 20, or 30°C for up to one year. Germination was testedin water and in polyethylene glycol 8000 solutions ( –0·2to –1·2 MPa osmotic potential) at 15, 20, 25 or30°C. Germination percentages and rates (inverse of meantimes to radicle emergence) were compared to those of newlyharvested, washed and dried seeds. For 40 and 60 DAA seeds,one year of storage at 20°C and water contents <6·5%significantly increased germination percentages and rates at20°C, but had little effect on germination at 25 and 30°C.Storage reduced the estimated base temperature (T_b) and meanbase water potential (_b) for germination of both 40 and 60 DAAseeds by approximately 5°C and 0·3 MPa, respectively.Immature 35 DAA seeds showed the greatest benefit from storageat 3 to 5% water content and 30°C, as germination percentagesand rates increased at all water potentials (). Storage underthese same conditions had little effect on the germination ofmature seeds in water, but increased germination percentagesand rates at reduced 's. Accelerated ageing for one month at30°C and water contents from 15 to 19° increased germinationrates and percentages of mature seeds at reduced 's, but longerdurations resulted in sharp declines in both parameters. Immatureseeds lost viability within one month under accelerated ageingconditions. An after-ripening period is required at all stagesof muskmelon seed development to expand the temperature andwater potential ranges allowing germination and to achieve maximumgerminability and vigour. Post-harvest dormancy is deepest atthe point of maximum seed dry weight accumulation and declinesthereafter, both in situ within the ripening fruit and duringdry storage. Key words: Muskmelon, Cucumis melo L., seed, development, dormancy, germination, vigour, after-ripening     

Respiratory rates in the cladoceran Ceriodaphnia dubia in Lake Rotongaio, a monomictic lake

The experimentally measured oxygen consumption rate by the cladoceran,Ceriodaphnia dubia, showed a linear increase between 5 and 20°C.Oxygen consumption rates of C. dubia were estimated in situfrom respiratory electron transport system (ETS) activity inLake Rotongaio during summer stratification and winter mixing.Oxygen consumption was 0.002 µl O₂ animal^–1 h^–1in the hypolimnion and 0.076 µl O₂ animal^–1 h^–1in the epilimnion during stratification. Implications of respiredoxygen for metabolic carbon requirements are discussed.     

Mechanisms Involved in Delayed Germination of Quercus nigra L. Seeds

Neither the pericarp nor the seed coat impose significant barriersto passage of water in Quercus nigra seeds. The pericarp eventuallybecomes limiting to continued swelling due to its mechanicalstrength. During stratification trapped gasses escape and continuedswelling of the cotyledons causes expansion of the pericarp.Vigorous acorns need around 105 days of combined stratificationand germination time to reach maximum germination. This additivityphenomenon is true for stratification times between 4 and 10weeks. Delayed germination is caused by at least three factors:(1) Mechanical strength of the pericarp, which was constantduring the observation period of 13 weeks; (2) Chemical inhibitionby the pericarp, which was alleviated by stratification forapproximately 4 weeks; (3) Slowly increasing capacity to imbibewater required for pericarp rupture. This component was apparentlynot dependent on temperature within the range of 5 to 30 °C,and operates during the entire stratification and germinationperiod. Quercus nigra L, water oak, seed germination, pericarp, stratification, dormancy     

The Structure and Cytochemistry of the Stigma-style Complex ofCorylus avellanaL. 'Tonda Gentile delle Langhe' (Corylaceae)

Structural and cytochemical aspects of the stigma-style complexofCorylus avellanawere studied. In cross section the stigmaticstyle consists of papillae, one or two layers of sub-epidermalcells and a central transmitting tissue. The papillae coverthe style for about 80% of its length, are unicellular and arecoated with a cuticle-pellicle. During development, the cellwalls of the papillae increase in thickness and between them,below the cuticle, lipid bodies are observed. The sub-epidermalcells are similar in cell content to the papillae. The centraltransmitting tissue consists of highly vacuolated cells andthe intercellular spaces are filled with a proteic and polysaccharidicsubstance. Both the transverse and longitudinal walls containplasmodesmata.Copyright 1998 Annals of Botany Company cytochemistry, stigma and style, ultrastructure,Corylus avellana     

The Role of ABA in the Control of Apple Seed Dormancy Re-appraised by Combined Gas Chromatography-Mass Spectrometry

Measured by GC—MS²—SIR³, endogenous ABA⁴ in embryonicaxes of seeds of Malus pumila L. cv. Golden Delicious decreased8-fold and cotyledon ABA by only 60%, during 10–50 d ofstratification at 5 ?C, after ABA leaching during an initial24 h soaking. During stratification, the percentage germinationof embryos transferred to 17?C showed a significant linear dependenceon log_e of ABA levels in the axes at transfer. Between 50 and70 d, ABA levels increased markedly in axes and testa both ofstratified seeds and seeds allowed to re-dry at 17 ?C afterinitial soaking. The ability of fully stratified axes with elevatedendogenous ABA to germinate indicated that stratification haddecreased their ABA sensitivity. Changes in cotyledon ABA couldnot account for the promotory effect of cotyledons on germinationduring the first 30 d of stratification. Loss of testa inhibitionof germination during stratification was not linked with changesin testa ABA. Stratification markedly increased the sequestrationin the axes of exogenous ABA supplied via the cotyledons. Changesboth in axis ABA levels and sensitivity were thus correlatedwith dormancy release, but subject to modifying control by thecotyledons and testa not involving ABA. Rehydration of driedseeds affected axis ABA later during storage via mechanismsunconnected with dormancy. Key words: ABA, seed dormancy, stratification