Reproductive Anatomy of the Grape-vine (Vitis vinifera L.): Origin and Development of the Anlage and its Derivatives

The origin and development of anlagen (undifferentiated primordia),inflorescences, tendrils and flowers in the grape cv. Shirazhas been investigated by scanning electron microscopy. Anlagenarise terminally by bisection of the apex of the so-called latentbud. The axis of the latent bud is continued by the originalapex and anlagen are displaced laterally. Micrographs presentedhere favour the interpretation of the grape-vine shoot as amonopodium. Anlagen formed distal to the 10th node of container grown vinesformed inflorescence primordia when plants were grown at hightemperatures (33°C day-28°C night). At lower temperatures(21°C day, 16°C night or 18°Cday, 13°C night)anlagen formed distal to the 10th node grew into tendril primordia.At basal nodes anlagen gave rise to shoot primordia. Each branchof the highly-divided inflorescence primordium of Shiraz formsfive flower primordia. Flower development is discussed.     

Response of Tulip Scale Mitochondria to Temperature in Relation to Cold Treatment of the Bulbs

A uniform batch of tulip bulbs were kept in the dark eitherat 2 °C or 18 °C. Sample bulbs were withdrawn at intervalsfrom both treatments and mitochondria were isolated from thescale tissue. Arrhenius plots of succinate and NADH oxidationby the mitochondria were made. Within the range 0–36 °C,mitochondria from uncooled bulbs showed a single transitionpoint at about 16 °C, as did mitochondria from freshly formeddaughter bulbs. In contrast, mitochondria from bulbs kept for 8 weeks or longerat 2 °C showed strong indications of two discontinuitiesin the Arrhenius diagrams within a similar temperature range,one about 10 °C below the other. The results suggest thattulip bulbs are chilling-sensitive, and that alterations inthe activation energies of certain oxidative enzymes in responseto accumulated cold treatment are necessary for metabolism tobe directed towards the growth of normal flowers.     

Changes in the Endogenous Growth Regulators in Bulbous Iris in Bulb-forming and Nonbulb-forming Aspects

Bulblets of 3–4 g of Dutch iris (Iris hollandica) cv.Dominator stored at 20°C and then grown at 15°C developedonly three or four leaves and bulbs formed at the base of eachleaf, whereas when grown at 25°C, they continued to growvegetatively with the development of 10 true leaves and didnot form any new bulb. This demonstrated that bulb formationin bulbous plants can be controlled by environmental factors.The levels of both abscisic acid and auxin activities increasedduring growth under the bulb-forming condition whereas onlyauxin activity increased under the nonbulb-forming condition.The coexistence of both abscisic acid and auxin seems to beessential in the processes of bulb formation. (Received August 22, 1980; Accepted November 26, 1980)     

Flower primordium formation at the Arabidopsis shoot apex: quantitative analysis of surface geometry and growth

Geometry changes, especially surface expansion, accompanying flower primordium formation are investigated at the reproductive shoot apex of Arabidopsis with the aid of a non-invasive replica method and a 3-D reconstruction algorithm. The observed changes are characteristic enough to differentiate the early development of flower primordium in Arabidopsis into distinct stages. Primordium formation starts from the fast and anisotropic growth at the periphery of the shoot apical meristem, with the maximum extension in the meridional direction. Surprisingly, the primordium first becomes a shallow crease, and it is only later that this shape changes into a bulge. The bulge is formed from the shallow crease due to slower and less anisotropic growth than at the onset of primordium formation. It is proposed that the shallow crease is the first axil, i.e. the axil of a putative rudimentary bract subtending the flower primordium proper, while the flower primordium proper is the bulge formed at the bottom of this axil. At the adaxial side of the bulge, the second axil (a narrow and deep crease) is formed setting the boundary between the flower primordium proper and the shoot apical meristem. Surface growth, leading to the formation of the second axil, is slow and anisotropic. This is similar to the previously described growth pattern at the boundary of the leaf primordium in Anagallis.     

The Effect of Storage Temperature on Shoot Growth, Flowering, and Carbohydrate Metabolism in Tulip Bulbs

Dry bulbs of the cvs. ‘Apeldoorn’ and ‘Paul Richter’ at stage G of flower development were stored at 5° or 21°C for 2, 4, 6, 8, 10, 12, and 14 weeks, respectively before being planted and forced at 18°C. Samples from each treatment were taken for carbohydrate analysis. The low temperature treatment (5°C) was necessary to obtain satisfactory shoot growth and flowering after planting. The rate of shoot growth and the percentage of flowering bulbs increased with increasing duration of the 5°C treatment. Time of flowering was also precipitated. 12–14 weeks of low temperature treatment seemed optimal. High temperature (21°C), or a short period at 5°C (2–6 weeks), resulted in many non-flowering bulbs, and a very slow shoot elongation when flowering occurred. In the latter case the tips or large areas of the perianths became white, the red pigmentation being prevented. Paper chromatographic analysis of oligosaccharides revealed a substantially increased content of sucrose and fructosyl sucrose (DP ≤ 5) during the first 2–4 weeks of cooling. At the end of 12 weeks at 5°C, the content of oligosaccharides decreased. The increase in the oligosaccharide content was accompanied by a corresponding starch decrease. High temperature storage (21°) led to comparatively slight changes in the sucrose and fructosyl sucrose content of the bulbs. The significance of carbohydrate metabolism in relation to shoot elongation and flowering is discussed.     

The role of ethylene in the flowering response of bulbous plants

Ethylene induces the flower formation and stimulates the flower-bud development of some bulbous plants exposed to the gas when the apex is in the vegetative state. For iris bulbs cv. Ideal maximum responses have been found after exposure to 5 ppm for 8 h; lower concentrations, shorter exposure periods and, depending on seasonal conditions, low temperatures during gas treatment, gave intermediate responses. The effects are opposite to the ethylene induced flower-bud blasting which occurs when bulbous plants are exposed to the gas after completion of the flower formation. Dry storage of the bulbs in atmospheres containing 5% CO₂ reduces the temperature-enhanced flower formation, suggesting a possible effect of endogenous ethylene. Presented at the International Symposium “Plant Growth Regulators” held on June 18–22 1984 at Liblice, Czechoslovakia.     

Temperature dependence of seedling establishment of a perennial, Dioscorea tokoro

The temperature dependence of seed germination and seedling growth was analyzed in Dioscorea tokoro, an East Asian summer-green perennial. Seeds were able to germinate fully only at 11°–20°C. At around 17°–20°C the first leaf petiole of the seedling elongated and quickly set the first leaf blade at a position enabling photosynthesis. At temperatures higher than 20°C petiole elongation was retarded, and seedlings formed a rhizome and established as a perennial. The rhizome size increased with temperature up to 29°C. Thus, during growth immediately after germination, temperature appears to be a key factor in determining whether the plant establishes as a perennial or grows rapidly without rhizome thickening. Received: April 6, 2001 / Accepted: September 14, 2001     

Sucrose-Modulated Morphogenesis in Anagallis arvensis L.

Sucrose was found to have a modulating effect on the morphogenesisof Anagallis arvensis L. leaves cultured in a Murashige-Skoogmedium. Root formation and growth seem to be more independentthan other morphogenetic expressions. Roots formed without exogenoussugars at 25°C but sucrose seemed to be necessary at 32and 35°C. Sucrose at 3% improved shoot formation at 25°Cand had an inhibitory effect at 6%concentration and 35°C.Shoot growth (internode length) is inhibited by sucrose concentrationshigher than 3%. Sucrose could also replace light irradiancein regulating shoot and leaf growth. A higher sucrose concentration,than that required for roots and shoots formation, is necessaryfor flower and fruit formation, but sucrose could not replacethe photoperiod requirement for flowering in culture medium. (Received June 17, 1985; Accepted December 24, 1985)     

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.     

A Quantitative Model of Reproductive Development in Cowpea [Vigna unguiculata (L) Walp.] in relation to Photoperiod and Temperature, and Implications for Screening Germplasm

Factorial combinations of four photoperiods (10 h, 11 h 40 min,13 h 20 min and 15 h) and three night temperatures (14, 19 and24 °C) combined with a single day temperature (30 °C)were imposed on nodulated plants of 11 cowpea accessions [Vignaunguiculata (L) Walp.] grown in pots in growth cabinets. Thetimes to first appearance of flower buds, open flowers and maturepods were recorded. Linear relationships were established betweenthe reciprocal of the times taken to flower and both mean diurnaltemperature and photoperiod. When the equations describing thesetwo responses are solved, the time to flower in any given photothermalregime is predicted by whichever solution calls for the greaterdelay in flowering. Thus in different circumstances floweringis controlled exclusively by either mean temperature or photoperiod.The value of the critical photoperiod is temperature-dependentand a further equation, derived from the first two, predictsthis relationship. Considered together as a quantitative modelthese relationships suggest simple field methods for screeninggenotypes to determine photo-thermal response surfaces. Vigna unguiculata (L) Walp., cowpea, reproductive development, photoperiod, temperature, germplasm     

Effects of Photoperiod, Nitrogen Nutrition and Temperature on Inflorescence Initiation and Development in Onion (Allium cepa L.)

The effects of photoperiod, nitrogen nutrition and temperatureon inflorescence initiation and development in onion cv. Rijnsburgerand cv. Senshyu Semi-globe Yellow were studied in controlledenvironments. Rates of inflorescence initiation were estimatedusing the data for leaf numbers formed prior to flower formationand the rates of leaf initiation. At 9 °C inflorescenceinitiation was accelerated by long photoperiods particularlyfor cv. Rijnsburger where the average time for initiation was86 days in 8 h and 38 days in 20 h photoperiods. Initiationwas as rapid at 12 °C as at 9 °C but was slower at 6°C. A reduction in the nitrate concentration in the nutrientsolution from 0.012 to 0.0018 M greatly accelerated inflorescenceinitiation particularly in photoperiods and temperatures notconducive to rapid initiation. Cv. Senshyu initiated more slowlythan cv. Rijnsburger and was less sensitive to photoperiod andnitrogen level. The development rate of inflorescences afterinitiation was accelerated by long photoperiods and increasesin temperature from 6 to 12 °C but was retarded by the lowernitrogen level. Allium cepa L., onion, flower initiation, inflorescence development, photoperiod, nitrogen nutrition, temperature, vernalization     

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     

Influence of temperature on growth, reproduction and longevity of Moina salina Daday, 1888 (Cladocera, Moinidae)

This paper presents the results of a study of the effects oftemperature on the growth, reproduction and longevity of thecladoceran Moina salina, a species of potential use as livefood in marine aquaculture. The growth rate of M.salina increasedwith increasing temperature. Some parameters of development,such as length at death and the number of adult instars, werealso positively related to temperature. Other parameters (durationof juvenile and adult instars) decreased with increasing temperature,while the number of juvenile instars was unaffected. An increasein temperature resulted in a reduction in age at maturity anda decrease in the number of days between broods. The numberof young per female, the number of broods per female, the numberof youngper day of reproductive life, and the number of youngper brood, increased up to a temperature of 25°C. At 15and 20°C. substantial degeneration of eggs and/or embryosoccurred. Likewise, temperature affected the type of reproductioncarried out by sexual females. Temperature and longevity wereinversely correlated. It was concluded that temperature actsas a very important factor regulating the life cycle of M.salina.Temperature >30°C may correspond to sublethal levels,while a temperature of 15°C is considered to impose stress.The range 20–25°C is optimal for the development andreproduction of this species.     

The Influence of Root Temperature, Rhizobium Strain and Host Selection on the Structure and Nitrogen-fixing Efficiency of the Root Nodules of Trifolium subterraneum

Low root temperature greatly affected the structure and N2-fixingefficiency of root nodules. More nodule tissue was formed perplant at 11 and 15 °C than at 7 and 19 °C. Low roottemperatures either prevented or slowed bacteroid differentiation;the differentiation zone was 19 per cent of the total noduletissue at 7 °C but only 5 per cent at 19 °C. The amount of bacteroid tissue formed at the different roottemperatures by the two fully effective strains TAi and SU297reflected the environment from which they originated. Both formedthe same amount at 15 and 19 °C but only TAI, which originatedfrom a cold environment formed bacteroids at 7 °C. At 7°C a bacteroid-filled cell did not degenerate until after20 days, cf. less than 10 days at 19 °C. At 7 and 11 °Call strains formed more bacteroids in the abundantly nodulatingthan in the sparse host independently of nodule number. Strain0403 was most sensitive to both temperature and host; it formedbacteroids in nodules on the sparse host at 19 °C only,but formed bacteroids in the abundant host between 7–19°C. The amount of bacteroid tissue formed by TAI and SU297 dependeddirectly on nodule number and was approximately constant between20–40 days only at 19 °C when nodule formation hadalmost stopped. The optimum temperature for maximum fixation of nitrogen wasnot necessarily that for maximum efficiency of fixation, whichfor these experiments was 51 ug N mm-3 bacteroid tissue perday.     

Root Growth of Bulbous Species during Winter

Bulbs of Allium moly, Scilla siberica, Triteleia uniflora, Tulipakaufmanniana and Narcissus lobularis were planted in a rhizotronand root growth was monitored weekly for an 18 week period.All the genera produced roots until the soil temperature droppedto 3 °C. Root outgrowth from the bulbs and growth of emergedroots then ceased or was strongly inhibited in N. lobularis,S. siberica and T. uniflora but not in the other genera. Mostbulbs resumed root elongation when the soil temperature hadwarmed to 4 °C. Root emergence and continued growth occurredfor a longer period during the winter than has generally beenassumed. Allium moly, Scilla siberica, Triteleia uniflora, Tulipa kaufmanniana, Narcissus lobularis, rhizotron, bulb, root growth     

Growth of Trifolium subterraneum L. Selected for Sparse and Abundant Nodulation as Affected by Root Temperature and Rhizobium Strain

Root temperature greatly affected plant growth whether or notplants depended on symbiotic nitrogen fixation. The two plantselections responded differently to the three strains of Rhizobiumand this response was differentially affected by root temperature. Plant yield was significantly decreased by each fall of 4 °Cin temperature from 19 to 7 °C by amounts that dependedboth on the host and Rhizobium strain. Symbiosis with strainTA1, originally isolated from a cold environment, was most tolerantof a root temperature of 11 °C; TA1 produced as much ormore plant material of the abundantly nodulating host in 40days growth at 7 and 11 °C as did the uninoculated plantsgiven KNO³. Root temperature affected the number, rate of formation, anddistribution of nodules on the root system. At 7 °C fewernodules formed than between 11 and 19 °C. At 7 °C nodulesdid not form on secondary roots by 40 days but at 11 °Cthe secondary roots nodulated rapidly between 30 and 40 days.Nodule formation at 19 °C was almost completed at 20 days,when secondary root nodules accounted for 60 per cent of thetotal. Within the range 15 to 19 °C, at which the originalselections for sparse and abundant nodulation were made, plantsnodulated true to selection, but not at 11 °C. At 7 and11 °C plants nodulated with TA1 yielded more with increasingnumber of nodules.     

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     

绵枣儿花芽分化的形态解剖学研究

为探明绵枣儿(Barnardia japonica)在哈尔滨地区的年生长节律以及花芽分化进程,该文以从长白山引种至东北林业大学花卉研究所苗圃内的绵枣儿为材料,采用田间观察法研究绵枣儿的年生长节律,并采用石蜡切片法观察其花芽分化各阶段的形态解剖学特征。结果表明:(1)绵枣儿在哈尔滨地区的生长节律大致可以分为四个时期,即花芽分化与发育期、开花期、结实期、休眠期。(2)绵枣儿花芽分化进程可以分为七个阶段,即4月中上旬,由于土壤温度较低,鳞茎仍处于未分化期; 4月下旬进入花序原基分化期; 5月上旬苞片原基分化; 5月下旬为小花原基分化期; 5月末至6月初花被片原基分化; 6月上旬进入雄蕊原基分化期; 6月下旬为雌蕊原基分化期。该研究明确了绵枣儿在哈尔滨地区的年生长节律和花芽分化各阶段的解剖学特性,为园林应用和新品种的选育提供了一定的科学依据。     

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.