Action du CCC et du B 995 sur la mise à fleur d'une plante bisannuelle,l'Œnothera biennis

Summary Oenothera biennis L. is a typical biennial plant with an absolute cold requirement for subsequent floral initiation under long-day conditions. Flowering of vernalized Oe. biennis is associated with transition from a rosette habit to the formation of a long flower-bearing stem. Vernalization in Oe. biennis consists of two consecutive stages: (1) preparation for flowering; (2) preparation of stem elongation. At the end of the second stage, the level of endogenous gibberellin-like substances is sufficient to allow the stem elongation which is requisite for subsequent floral development.Applications of (2-chloroethyl)trimethylammonium chloride (CCC) via the roots, when made after the cold treatment, have no effect on internodal elongation and subsequent flowering of vernalized Oe. biennis. Relatively small amounts of CCC applied onto the apical bud of the rosette promote stem growth. However, 750 g of CCC act as a growth inhibitor and delay the beginning of stem elongation but this retardant has no effect on the number of flower buds.In contrast, N-dimethylaminosuccinamic acid (B 995), when applied after a cold treatment, delays the beginning of stem growth, this delay increasing with greater amounts of applied B 995. However, with relatively small amounts of B 995, the rate of later stem growth increases rapidly so that treated plants flower at the same time as controls.If gibberellic acid (GA₃) is applied on the apical bud just at the same time as B 995, it reverses the effects of the growth retardant, even when the amount of B 995, applied by itself, is sufficient to inhibit entirely stem elongation and flowering.B 995 is particularly effective if the preceding cold treatment was just sufficient for effective vernalization. If the cold treatment was extended beyond this time, a greater amount of retardant was required to obtain the same degree of stem growth inhibition.B 995 probably acts by interference with the metabolism of endogenous gibberellin-like substances. The delay of floral initiation in vernalized Oe. biennis by B 995 is a consequence of the retarded internode elongation; if this retardation exceeds a certain limit, the plant is devernalized and exhibits a cold requirement identical with the original one.     

INHIBITORY EFFECT OF GROWTH RETARDANTS ON THE INDUCTION OF FLOWERING IN WINTER WHEAT

1. Growth retardants, CCC, Amo-1618, Phosfon-D and B-995, appliedduring seed vernalization inhibited the ear development of winterwheat. CCC applied during green plant vernalization inhibitedflowering,but it had no appreciable effect on the final stemlength. Theinhibition by CCC was reversed by foliar applicationof gibberellin.On the other hand, CCC applied after the vernalizationperiodaffected the final stem length but not flowering.
2. Theamount of endogenous gibberellin-like substance(s) was greaterin the vernalized plant than in the non-vernalized plant. Nogibberellin-like substance was detected in the CCC-treated plant.
3. Endogenous gibberellin-like substance(s), whose biosynthesisis inhibited by some growth retardants, may play a part in thevernalization process in winter wheat.

¹Present address: National Institute of Agricultural Sciences,Nishigahara, Kitaku, Tokyo     

CONTROL OF FLOWER FORMATION BY GROWTH RETARDANTS AND GIBBERELLIN IN SAMOLUS PARVIFLORUS,A LONG-DAY PLANT

The growth retardants AMO–1618 and CCC inhibited flower formation and stem elongation in Samolus parviflorus, a long-day rosette plant, under inductive conditions. The vegetative growth of the plants, as measured by leaf formation, was affected only slightly, or not affected at all. Application of gibberellic acid (GA₃) reversed completely the inhibition both of flower formation and of stem elongation caused by AMO, but relatively larger amounts of GA were required to reverse the CCC inhibition of stem elongation than that of flower formation. When applied under short-day conditions, AMO had no effect on the level of applied GA required for flower induction. When applied following long-day treatment the retardant caused some reduction of flower formation after marginal numbers of long days, but had no effect when enough long days to cause 100% flower formation were given. Other evidence indicates that the growth retardants act by inhibiting the synthesis of endogenous gibberellin. In LD plants, at least part of the action of inductive environmental conditions consists in causing an increase of gibberellin synthesis, supporting the hypothesis that relatively high GA levels are necessary for the production of the floral stimulus in this group of plants, as in long-short-day plants. The experiments with CCC indicate that stem elongation and flower formation in Samolus can be separated, and that the effect of GA on flower formation is not necessarily dependent on its effect on stem elongation.     

Translocation of leaf-fed 32P in pea plants as influenced by foliar and root applications of CCC and Phosfon

In controlled environment growth chambers, the effects of foliar and root applications of 2-chloroethyltrimethylammonium chloride (CCC) and 2,4-dichlorobenzyltributylphosphonium chloride (Phosfon) on the translocation of³²P fed to leaves, were investigated. When applied to leaves or to root, CCC had no effect on the relative amounts of³²P radioactivity retained by the fed leaf 5, 20 and 80 h after feeding. At 20 and 80 h after feeding, Phosfon concentrations of 0.01 and 0.1mg l^?1 reduced retention of the applied³²P. 80 h after³²P feeding, CCC concentration of 1 mg l^?1 applied as a foliar spray or to the root enhanced the downward movement of³²P. Phosfon at low concentrations, particularly at 0.1 mg l^?1, on the other hand, favoured an upward transport of the applied³²P. Foliar applications of CCC and Phosfon at high concentrations had no significant effect on³²P transport to the root and the shoot below the fed leaf, while root applications of CCC and of Phosfon inhibited downward transport. Root applications generally caused greater alterations in³²P distribution patterns than did foliar applications. On the basis of total active ingredient uptake, Phosfon was more effective than CCC in altering translocation patterns.     

Modification of growth habit of Majestic potato by growth regulators applied at different times

The effect of gibberellic acid, CCC (2-chloroethyltrimethylammonium chloride) and B 9 (N-dimethylaminosuccinamic acid) was studied on growth of potato plants in pots. Growth was analysed on four occasions and changes in habit defined in terms of internode lengths, leaf areas and growth of lateral branches. Soaking seed pieces for 1 hr. in GA solution caused six internodes to elongate greatly, an effect not prevented by CCC applied when the shoot emerged from the soil. The effects on internode extension were determined by the length of the interval between GA treatment and CCC treatment. Treatment at emergence with CCC shortened all internodes and more CCC applied 4 weeks later had no effect. Late application of CCC or B9 shortened the top two lateral branches, usually very long in untreated plants. The regulators affected leaf growth differently from internode growth: usually growth regulators had less effect on leaf growth. Effects on growth depended on when the regulators were applied. Treatment with GA alone inhibited bud development at higher nodes than in untreated plants; when followed by late treatment with CCC, lateral growth at higher nodes was also less. CCC retarded development of lateral branches especially when applied early. B9 had a similar effect to CCC applied late. When regulators retarded growth of lower laterals, upper laterals often grew more than in untreated plants. Treatments did not affect the number of leaves on the main stem at first but later GA hastened senescence. GA increased the number of leaves on lateral stems, and the effect was enhanced by CCC. CCC alone increased the number of first- and second-order lateral leaves. GA lengthened and CCC shortened stolons. The effect of CCC persisted throughout the life of the plant. CCC or B 9 shortened stolons whenever applied. CCC hastened tuber initiation but slowed tuber growth. CCC at first retarded formation of lateral tubers but had no effect on the ultimate numbers of lateral and terminal tubers. The value of E (net assimilation rate) did not alter with time. CCC applied at emergence increased E, probably because it hastened tuber initiation and temporarily increased sink capacity. Although tubers formed earlier with CCC, their growth was slower and their demand for carbohydrate was also less. The increase in second-order laterals in CCC-treated plants indicates that they utilize carbohydrate that would normally go to tubers. This experiment also demonstrates that crowding leaves by shortening stems did not diminish E, possibly because another over-riding process (bigger sinks) offsets the effect of shading.     

Plant resistance to Myzus persicae induced by a plant regulator and measured by aphid relative growth rate

Myzus persicae showed a reduced relative growth rate on plants given soil drenches of 1% CCC (a plant growth retardant), and a greater reduction when CCC was applied as a foliar spray. The use of the relative growth rate of aphids as a convenient measure of their performance in relation to plant resistance is discussed.

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Zusammenfassung Die Resistenz von Kohlpflanzen, die mit 1% CCC (einem Regulator des Pflanzenwachstums) behandelt worden waren, gegen Myzus persicae wurde mit Hilfe des Wachstumsquotienten der Blattläuse (g/g/Tag) gemessen. Diese Methode arbeitet rasch und ergibt eine ziemlich geringe Variabilität. Der Maßstab scheint sinnvoll und ziemlich empfindlich zu sein.Mit CCC gedüngte Pflanzen zeigten stets eine ziemlich starke Verminderung des Wachstumsquotienten von Myzus persicae. Wurde CCC auf die Pflanzen aufgesprüht, so ergab sich ein noch geringerer Wachstumsquotient der Blattläuse.

     

Über den Gibberellingehalt von Zwerg- und Normalerbsen im Rotlicht und die Wirkung von Chlorcholinchlorid auf das Wachstum der Erbsen

Zusammenfassung Keimlinge von Zwerg- und Normalerbsen wurden auf ihren Gibberellingehalt getestet. Die Normalerbsen enthalten etwa achtmal soviel wie die Zwerge von der Gibberellinfraktion I nach Kende und Lang, die auf Normalerbsen stark, auf Zwerge kaum wirkt.Beide Rassen wurden mit Chlorcholinchlorid, einem Hemmstoff der Gibberellinsynthese bei Fusarium, behandelt. Im Rotlicht werden die normalen Pflanzen verzwergt, doch im Dunkeln hat die Substanz nur einen geringen Effekt. Die Dunkelhemmung ist so groß wie die Hemmung der Zwerge in Rotlicht. Eine mögliche Erklärung für die Unwirksamkeit von CCC im Dunkeln ist, daß die Erbsen im Dunkeln zum Wachstum kein oder nur wenig Gibberellin benötigen.

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The content of gibberellin-like substances in dwarf and normal peas growing in red light, and the effect of chlorocholinchloride on growth of peas

Summary Dwarf and normal pea seedlings were extracted and their gibberellinlike substances bioassayed. The normal peas yield about 8 times as much as the dwarfs of gibberellin-fraction I after Kende and Lang, which is highly effective on normal peas but nearly without effect on dwarfs.Both cultivars were treated with the inhibitor of gibberellin-synthesis in the fungus Fusarium, chlorocholinchloride (CCC). In red light the normal plants are dwarfed, but in darkness this substance has only a weak inhibiting effect on growth. The inhibition in darkness is of the same magnitude as the effect of CCC on dwarfs growing in red light. A possible explanation for the ineffectiveness of CCC in darkness is that peas need there no gibberellin at all or only very minute amounts for growth.

     

Effect of Pot Size and Timing of Plant Growth Regulator Treatments on Growth and Tuber Yield in Greenhouse-Grown Norland and Russet Burbank Potatoes

The effects of pot size, timing of the application of paclobutrazol (PTZ) and gibberellic acid (GA₃), and the counteractive effect of these two compounds on growth and tuber yield of greenhouse-grown Norland and Russet Burbank potatoes were investigated. Plants were grown either in 1.5-liter pots (15 cm deep) or 3.0-liter pots (18 cm deep) and received a foliar application of either 1.5 mm PTZ or 9 × 10⁻³ mm GA₃ at early or late stolon initiation. Some plants that had been foliar treated with 1.5 mm PTZ at early stolon initiation were foliar treated with 9 × 10⁻³ mm GA₃ at late stolon initiation. PTZ reduced haulm length in both cultivars significantly, particularly when the treatment was applied at early stolon initiation, but the late treatment reduced haulm length only when growing in 3.0-liter pots. Irrespective of the timing of treatment, GA₃ increased haulm length in Norland growing in both pot sizes, but the treatment increased haulm length in Russet Burbank only when applied at late stolon initiation. GA₃ applied after PTZ did not overcome the growth-inhibiting effect of the PTZ treatment. The PTZ treatment effectively increased usable tuber number/plant (UTN) in Norland, but PTZ had no effect on UTN in Russet Burbank. PTZ reduced usable tuber weight/plant (UTW) only in Norland growing in 1.5-liter pots. By contrast, GA₃ increased UTN only when treated at late stolon initiation of 1.5-liter pot-grown Norland, whereas the same treatment was effective when applied only at early stolon initiation for Russet Burbank. For Norland, the increase in UTN by early applied PTZ was reduced by the subsequent application of GA₃. The use of 3.0-liter pots for minituber production in both Norland and Russet Burbank appears to have no advantage over growing in 1.5-liter pots, particularly when PTZ or GA₃ is used to enhance tuberization. Received May 30, 1997; accepted February 3, 1998     

The Effects of Foliar Applications of (2-Chloroethyl)-trimethylammonium Chloride on Leaf Area and Dry Matter Production by the Brussels Sprout Plant

When CCC was applied as a spray to the leaves of Brassica oleraceaL. (Brussels sprout) grown in pots, plant height and mean internodelength were reduced. The effects appeared more slowly and wereless pronounced than those previously observed when CCC hadbeen applied to the soil; other differences were that root growthwas not inhibited, stem weight was only significantly reducedat the highest rate of application (2 per cent), and stomatalnumber per unit area of lower leaf epidermis was not affected.In common with soil applications, leaf thickness, stem diameter,and the percentage moisture contents of the leaves were allincreased by foliar applications.In a further experiment theprogress of wilting was observed in untreated plants and inplants treated with CCC applied either to the leaves or to thesoil. The rates of water loss and the moisture contents of theleaf laminae of the treated plants, after a period of wilting,were not significantly different from the controls. The treatedplants, however, looked less ‘wilted‘ for the changein angle of the leaf lamina to the stem was less and their leaveswere therefore held more upright.     

Effects of Chlorocholine Chloride and Water Regime on Growth, Yield, and Water Use of Spring Wheat

When CCC was applied as a spray to the leaves of Brassica oleraceaL. (Brussels sprout) grown in pots, plant height and mean internodelength were reduced. The effects appeared more slowly and wereless pronounced than those previously observed when CCC hadbeen applied to the soil; other differences were that root growthwas not inhibited, stem weight was only significantly reducedat the highest rate of application (2 per cent), and stomatalnumber per unit area of lower leaf epidermis was not affected.In common with soil applications, leaf thickness, stem diameter,and the percentage moisture contents of the leaves were allincreased by foliar applications.In a further experiment theprogress of wilting was observed in untreated plants and inplants treated with CCC applied either to the leaves or to thesoil. The rates of water loss and the moisture contents of theleaf laminae of the treated plants, after a period of wilting,were not significantly different from the controls. The treatedplants, however, looked less ‘wilted‘ for the changein angle of the leaf lamina to the stem was less and their leaveswere therefore held more upright.     

Persistent effects of seedling treatment on growth of sugar beet in pots

Further evidence is provided that the environment of sugar-beet seedlings, or growth substances applied to seedlings, continues to influence growth when the plants are later in other environments. Sugar-beet seeds were germinated at 20 °C in 8, 16 or 24 h photoperiods of constant light intensity, i.e. with different amounts of total radiation. When the seedlings had two leaves (15–18 days old) they were transferred to large pots in the glasshouse. Some seedlings were treated with (2-chloroethyltrimethylammonium chloride) either sprayed on the leaves or applied to the soil, at different times. The treatments affected areas of individual leaves throughout the growing period; plants raised in 24 h photoperiod had the largest leaves, and those in 8 h photoperiod the smallest. Consequently, 24 h plants had most dry matter and 8 h plants least. Plants given most radiation produced leaves fastest and CCC applied early increased the rate, but as the leaves were smaller, except late in 1967, and died sooner, the leaf area duration was less and so yields were less. CCC applied later did not affect leaf production. There was no interaction between amount of radiation and CCC treatment. Twenty-four hour plants had the greatest net assimilation rate (E) early. CCC decreased E early, but increased it later and more when sprayed on the leaves than when applied to the soil. Some factor, possibly pot size, eventually restricted growth and probably diminished the effect of the treatments applied to the seedlings.     

Effect of Gibberellin on Growth, Protein Secretion, and Starch Accumulation in Maize Endosperm Suspension Cells

The physiologic effect of gibberellins (GA) in seed development is poorly understood. We examined the effect of gibberellic acid (GA₃) on growth, protein secretion, and starch accumulation in cultured maize (Zea mays L.) endosperm suspension cells. GA₃ (5 and 30 μm) increased the fresh weight, dry weight, and protein content of the cultured cells, but the effect of GA₃ at 50 μm was not significantly different. However, the protein content in the culture medium was increased by these three concentrations of GA₃. The effect of GA₃ on the amount of cellular structural polysaccharides was not significant, but GA₃ had a dramatic effect on the starch content. At 5 μm, GA₃ caused an increase in the starch content, but at 50 μm the starch accumulation was reduced. Chlorocholine chloride (CCC), an inhibitor of GA biosynthesis, significantly increased the starch content and decreased the structural polysaccharide content of the cultured cells. The effects of CCC at 500 μm on the starch and polysaccharide content were partially reversed by 5 μm GA₃ applied exogenously. Based on these results we suggest that GA does not favor starch accumulation in the cell cultures and that the addition of lower concentrations of GA₃ in the medium may provide an improved balance among the endogenous GA in the cultured cells. Received October 31, 1995; accepted March 25, 1997     

Effetti Morfologici,Anatomici Ed Ultrastrutturali Indotti Dai Ritardanti Di Crescita Su Plantule Di Pisum Sativum L. Var. « Gloria Di Quimper » Cultivate in Soluzione Nutritizia

Abstract

The effect of the growth retardants on the structure of Pea seedlings coltured in nutritive solution. – The addition of CCC (2-Chloro-ethyltrimethyl ammonium chloride) and AMO 1618 (4-Hydroxyl-5-isopropyl-2 methyl-phenyl-trimethylammonium chloride. 1-piperidine carboxylate) to Pea seedlings (Pisum sativum L. var. Gloria di Quimper) promotes the usual modifications induced by growth retardants on higher plants. CCC appears less effective than AMO 1618; CCC inhibits growth only at 10²-M. concentration, on the contrary 5×10-⁵M. AMO 1618 inhibits strongly the growth of the seedlings both in the light and in darkness. CCC and AMO 1618 operate similarly as far as the inhibition of expansion growth, the increase of the stem diameter, and the decrease of the apical dominance are concerned. 10-²M. CCC stimulates both the growth of roots and the secondary roots formation, on the contrary 2,5×10-⁴M. AMO 1618 inhibits strongly the growth of the roots. AMO 1618 affects more strongly than CCC the expantion growth of the leaves. Leaves of the AMO 1618 treated plants are greener than the control plants. Plants treated with CCC and AMO 1618 are smaller because these chemicals inhibit the expantion growth of the cells. The increase of the stem diameter induced by CCC and AMO 1618 is due to the stimulation of the mitotic activity of the cambium. AMO and CCC induce a decrease of the size of the vessels and the sieve tubes. In the sieve tubes of the treated plants and slime plugs appear near to the sieve plates many slime bodies. AMO and CCC did not affect the mitotic activity of the apical meristems; in fact the plants grown in the presence of the growth retardants, show a normal primary body. AMO and CCC delay the lignification process. Chloroplasts of this Pisum sativum variety show prolamellary bodies associated to a good lamellar system. Starch granules are always present. Starch was never found in the chloroplasts of the treated plants. The general picture of the effects induced by growth retardants in Pea seedlings show so many modifications that it is very difficult to believe, like some Authors suggest, that all the effects produced by growth retardants are due to the inhibition of gibberellin biosynthesis.     

Uptake and translocation of root-fed32P in response to foliar and root applications of CCC and phosfon inPisum sativum

The uptake and translocation of³²P applied to nutrient solutions, as influenced by (2-chloroethyl) trimethylammonium chloride (CCC) and 2, 4-dichlorobenzyltributylphosphonium chloride (Phosfon), were investigated in growth chambers. Specific effects depended on the “Retardin”, the method of application, and the concentration. Foliar applications of CCC had no significant effect on³²P uptake 5 h after feeding. At 20 and 80h after feeding, CCC at 100 and at 1 000 mg l^?1 decreased P uptake. With root applications of CCC the same concentrations decreased P uptake as early as 5h after feeding, while the 1 mg l^?1 concentration enhanced P uptake by 40% after 20h. Both the foliar and the root applications of Phosfon influenced P uptake 5h after feeding. With foliar applications the low Phosfon concentration of 0.01 mg l^?1 increased P uptake throughout the experimental period of 80h, but the magnitudes of enhancement declined from 109% at 5h to 63% at 80h. Similarly, the enhancement of P uptake due to the 0.1 mg l^?1 foliar treatment declined from 132% at 5h to 80% at 80h. 100 mg l^?1 CCC enhanced P translocation to the shoot in 5h, with magnitudes of 29% (foliar application) and 64% (root application). At 20 and 80h the stimulations were nullified. The highest concentrations (100 mg l^?1 CCC; 10 mg l^?1 Phosfon) enhanced P translocation 80h after feeding. There were thus general enhancements of P uptake at low concentrations and suppressions at high concentrations, but these effects diminished with time, indicating transitory influences.     

Effect of gibberellins and the growth retardant CCC on the nodulation of soya

Summary The effect of exogenous applications of gibberellins (GAs) or the growth retardant -chloroethyltrimethylammonium chloride (CCC) on root nodule formation and activity (C₂H₂-reduction) in soya was studied. Daily foliar application of GA₃ (2.89×10^–6 M) delayed the formation of nodule initials and reduced the numbers mass nodule^–1 and specific activity of nodules by 43%, 31% and 47% respectively, without affecting plant growth. Similar effects on nodulation were produced by foliar application of GA₄ (3.01×10^–5 M) or GA₇ (3.03×10^–5 M), or by the addition of GA₃ (2.89×10^–6 M) to the rooting medium. GA effectiveness in reducing nodule numbers was decreased by delaying its application until after the initial infection process had occurred, but the nodules formed were smaller and less active than those of the untreated control plants. The GA effect on nodulation and nodule activity was not associated with alterations in root exudate or due to a direct inhibitory effect of the hormone on the nitrogenase system. When the endogenous root content of GA-like substances was reduced (86% decrease) by foliar application of CCC (6.30×10^–5 M), nodule numbers were increased by 56%, but nodule size and total nodule activity were similar to those of control plants. The GA and CCC treatments had no effect on rhizobial growth in liquid culture nor on root colonisation by rhizobia.The results suggest that the endogenous content of root GA may have a regulatory role in both the infection process and in subsequent nodule morphogenesis, thus controlling both the number and effectiveness of the root nodules formed.     

Interaction of Growth Retardants and Temperature in Growth, Flowering, Regeneration, and Auxin Activity of Begonia × cheimantha Everett

Soil application of CCC reduced stem and leaf growth in Begonia plants. This effect was evident with all concentrations tested at 18°C, whereas at 21 and 24°C no growth–retarding effect was observed with 2 × 10^?2 M CCC, and with 5 × 10^?3 M growth was even stimulated. Flowering was promoted by CCC in long day and neur–critical temperature, particularly under low light intensity in the winter. The formation of adventitious buds in leaves of plants grown at 21 and 24°C was stimulated when the plants received 5 × 10^?2 and 2 × 10^?2 M CCC, while 8 7times; 10^?2 M was inhibitory. In plants grown at 18°C bud formation was inhibited by all CCC concentrations. Root formation in the the leaves was usually stimulated by high CCC concentrations, while root elongation was reduced. The level of ether–extractable. acidic auxin (presumably IAA) in the leaves was lowered by CCC treatment of the plants, hut this required higher CCC concentrations at higt than at low temperature. When applied to detached leaves CCC stimulated bud formation at concentrations ranging from 10^?4 to 10^?2 M in leaves planted at 18 and 21°C. At 24°C budding was inhibited by 10^?2 M CCC, the lower concentrations being stimulatory also at this temperature. Root formation and growth were not much affected by CCC treatment of the leaves, but increased with the temperature. Soil application of Phosfon (4 × 10^?4 M) had no effect on growth and flowering, nov did it affect the subsequent regeneration of buds and roots in the leaves. In detached leaves Phosfon stimulated bud formation with au optimum at 10^?6 M. Root formation was stimulated by Phosfon at all temperatures, the optimal concentration being 10^?5 M, whereas root length was conversely affected. Foliar application of B-995 to intact plants and treatment of detached leaves greatly inhibited the formation of buds and had little effect on root formation. B-99D reduced the growth and delayed flowering in the plants.     

Effect of two plant growth retardants on steviol glycosides content and antioxidant capacity in Stevia (Stevia rebaudiana Bertoni)

Two greenhouse experiments were conducted to study the effect of two plant growth retardants, Chlorocholine chloride (CCC) and Paclobutrazol (PBZ), on growth, Steviol glycosides (SVglys) content and antioxidant capacity in Stevia (Stevia rebaudiana Bertoni). Five concentrations of CCC (0, 250, 500, 750 and 1,000 ppm) and PBZ (0, 6, 12, 18 and 24 ppm) with three replications were applied to Stevia plants as treatments based on completely randomized design. CCC was sprayed on Stevia shoots, but PBZ was applied as a drench. The obtained results showed that CCC reduced plant height but improved leaf and stem dry weight, especially with 750 ppm concentration. Total SVgly content and consequently SVglys yield were significantly reduced by CCC application, and 1,000 ppm of CCC concentration was more effective than other treatments. PBZ had no effect on Stevia height while it significantly enhanced stem and dry weight at 12 ppm. Moreover, PBZ remarkably increased total SVglys contents, SVglys yield, and Rebaudioside A/Stevioside ratio. Total antioxidant capacity significantly varied with CCC and PBZ and the highest activity was obtained with 1,000 and 12 ppm of CCC and PBZ, respectively. The results of these experiments indicated that, although CCC and PBZ are plant growth retardants and act as anti-gibberellins, only CCC reduced plant height and SVglys production in Stevia. On the contrary, PBZ at 12 ppm concentration, improved Stevia growth, SVglys production, and antioxidant capacity.     

The Interaction of (2-Chloroethyl) trimethylammonium Chloride and Gibberellic Acid in Strawberry

Applications of (2-chloroethyl) trimethylammonium chloride (CCC), by foliar spray or to the soil, shortened petioles and decreased top and root growth of strawberry plants. Application of gibberellic acid increased petiole length and fresh weights of tops but not of roots. Applied together gibberellic acid overcame the depression of growth in weight of tops induced by CCC and countered the depression in petiole lengths. Gibberellic acid induced elongation of internodes of the vegetative stem and the elongation was increased substantially by concurrent application of CCC. This synergism in stem growth indicates a lack of antagonism between CCC and exogenous gibberellic acid in strawberry. The implications are discussed.     

Effects of leaf nitrogen availability and leaf position on nitrogen allocation patterns in Vaccinium vitis-idaea and Vaccinium uliginosum

Summary Nitrogen allocation patterns from leaves of Vaccinium vitis-idaea (evergreen) and Vaccinium uliginosum (deciduous) were assessed using a foliar application of ¹⁵N labeled ammonium sulfate. These are wild perennial shrubs inhabiting arctic and subarctic regions. More label was transported from labeled leaves of Vaccinium uliginosum then Vaccinium vitis-idaea. In Vaccinium uliginosum, the amount of label transported from the labeled leaf increased as the concentration of nitrogen in the label increased. Current growth in Vaccinium uliginosum was a strong sink for nitrogen because most of the ¹⁵N transported from the labeled leaf was contained in this region. In addition, when greater quantities of nitrogen were applied, larger quantities were retained in current growth. Current growth of Vaccinium vitis-idaea, on the other hand, was not as strong a sink because regardless of the nitrogen available thru various label concentrations, the enrichment of current growth was not affected and was not significantly different from older stems or leaves. Yet, in both species, nitrogen was transported freely from leaves of all positions along the stem to all parts of the plant including roots and rhizomes. The position of the leaf along the stem had no effect on the patterns of allocation to other organs.     

CCC and Prohexadione-Ca Enhance Rhizome Growth and Lateral Bud Production in Rhubarb (<Emphasis Type="Italic">Rheum rhabarbarum</Emphasis> L.)

Accelerating rhizome growth is crucial to enhancing propagule production in rhubarb (Rheum rhabarbarum L.) because the crop is propagated through rhizome divisions. This can be achieved through manipulating source-sink activity. This study tested the hypothesis that synthetic plant growth retardants Prohexadione-Ca and CCC enhance rhizome growth in rhubarb. Two different concentrations of these plant growth retardants and GA₃ (positive control) were foliarly applied on the cultivar German Wine at three stages of shoot growth under greenhouse conditions. Both Prohexadione-Ca and CCC favorably enhanced rhizome growth through suppressing shoot growth. CCC at 3000 mg L⁻¹ produced the best results and the effect was apparent when applied at 12 weeks after shoot emergence. The rhizome diameter, fresh weight, and the number of viable buds were enhanced significantly in plants sprayed with CCC 3000 mg L⁻¹. Both Prohexadione-Ca and CCC were equally effective in enhancing dry mass and starch allocation preferentially toward the rhizome. Prohexadione-Ca- and CCC-induced rhizome growth enhancement could possibly be due to their known role as GA biosynthesis inhibitors or through increasing photosynthetic efficiency and preferentially reallocating carbohydrates to the rhizome.