Studies on the stimulation of abscission by malformin on cuttings of Phaseolus aureus Roxb

White light irradiance required for complete and slight inhibitionof malformin-induced abscission by cuttings of Phaseolus aureuswas 13.5?10³ and 0.1?10³ ergs/cm^2. sec, respectively. Longerphotoperiods and higher irradiances were required to inhibitabscission by malformin-treated cuttings than by controls. Malforminstimulated dark abscission more rapidly, and at lower concentrations,than Ethrel or abscisic acid. The ability of light to inhibitmalformin-induced abscission diminished rapidly after 36 hrin the dark. Malformin accelerated chlorophyll and fresh anddry weight loss of leaves in the dark. The loss in fresh anddry weight, and perhaps chlorophyll, were inhibited by light.Hydroxyproline had little effect, but sucrose, hadacidin, kinetinand indoleacetic acid delayed malformin-induced abscission.Although puromycin, an inhibitor of protein synthesis, stimulatedabscission on controls, it inhibited malformin-induced abscission. (Received July 18, 1977; )     

Effect of malformin on phytochrome reactions in Vigna and Avena

The rate of destruction of the far red absorbing form of phytochrome(Pfr) in green or etiolated cuttings of Vigna radiata was slowerin the presence of malformin than in its absence. Malforminhad no effect on the accumulation of total phytochrome in thedark, or on the reaccumulation of phytochrome after destructionin red light. The amount of photoconversion of the red absorbingform of phytochrome (Pr) to Pfr or Pfr to Pr by given dosesof red or far red radiation was slightly but consistently lessin malformin-treated cuttings of V. radiata than in controls.Malformin had no effect on the rate of destruction or photoconversionof phytochrome in etiolated shoots of Avena sativa. The decreasein destruction rate of Pfr by malformin in V. radiata may contributeto the inhibition of dark abscission by malformin after lighttreatment. (Received October 3, 1979; )     

Factors Influencing Induction of Resistance to Dark Abscission by Malformin

Factors influencing induction of resistance to dark abscissionby malformin on cuttings of Vigna radiata during treatment inlight were examined. When light duration (13.5 W m^–2)increased from 0 to 48 h, the effect of malformin on subsequentdark abscission changed from stimulation only (0 to 4 h), stimulationfollowed by inhibition (8 to 12 h), to inhibition only (24 to48 h). Maximum abscission resistance occurred after 48 h whenirradiance was 6.6 W m^–2. Kinetin treatment in light reducedsubsequent dark abscission by controls but did not reduce abscissionon malformintreated cuttings. Hadacidin had no effect on inductionof abscission resistance by malformin. IAA, hydroxyproline,CaCl₂, sucrose, and NH₄NO₃ were inactive. ABA and ethephon completelyblocked induction of abscission resistance by malformin. Inhibitionof abscission induced by kinetin was also blocked by ABA. Becauseboth puromycin and malformin inhibited dark abscission followingtreatment in light, malformin may induce abscission resistanceby inhibiting protein synthesis or promoting formation of othersubstances which inhibit protein synthesis. Leaf blade removalfrom the distal end of the petioles abolished malformin-inducedabscission resistance. It is suggested that in light malformininduces formation of abscission-inhibiting compounds in leaveswhich are responsible for development of abscission resistance. (Received May 17, 1983; Accepted November 8, 1983)     

Phytochrome involvement in the induction of resistance to dark abscission by malformin

The active portion of the visible spectrum which is required for malformin to produce leaves which are resistant to dark abscission from cuttings of Phaseolus aureus is red light. Abscission resistance was partially to almost completely lost by far irradiation prior to dark incubation. Although Ethrel, an ethylene releasing compound, stimulated dark abscission of resistant and control leaves, resistance was not lost because control leaves always abscised at a greater rate. The participation of phytochrome in the induction of abscission resistance by malformin is indicated.Abbreviations Pfr far-red absorbing form of the phytochrome system - R red radiation - FR far-red radiation - D dark     

Malformin negates the Inhibition of Ethrel-induced Leaf Abscission by AgNO3

In light, malformin completely abolished the ability of Ag⁺to inhibit Ethrel-induced leaf abscission from cuttings of Vignaradiata, even though Ag⁺ was applied 24 hr before malformin.Malformin itself did not induce abscission in the light. However,Ag⁺ was active on cuttings which had been pre-treated with malforminfor 2 days in the light. No evidence was obtained to suggestreaction between malformin and Ag⁺. In the dark, Ag⁺ had noeffect on stimulation of leaf abscission by malformin. (Received March 7, 1981; Accepted May 12, 1981)     

Abscission: ethylene and light control

The role of ethylene in light control of leaf abscission im mung bean, Vigna radiata (L.) Wilczek cv Jumbo, cuttings was examined. While red light inhibits and far-red light promotes loss of break strength in abscission zones as compared with dark controls, changes in the rate of abscission could not be associated with changes in the rate of ethylene production. Reducing ethylene synthesis in tissue with aminoethoxyvinylglycine did not alter the effects of red or far-red light on abscission. Far-red light appeared to increase and red light appeared to decrease tissue sensitivity to ethylene.     

Abscission: characterization of light control

Exposure of mung bean (Vigna radiata [L.] Wilczek cv Jumbo) cuttings to low level red light inhibits dark-induced leaf abscission. A 12-hour daily light requirement for maximum inhibition of abscission was equally effective as a continuous red light treatment or shorter light-dark cycles. Transfer of cuttings from dark to light stopped the abscission process at the time of transfer. The available evidence suggests a light receptor located in the leaves with an abscission inhibitor translocated from lighted leaf to the abscission zone.     

Abscission: Response to Red and Far-Red Light

Craker, L. E., Zhao, S. Y. and Decoteau, D. R. 1987. Abscission:response to red and far-red light.—J. exp. Bot. 38: 883–888. The dose-response and time relationship of red and far-red lightin the inhibition and promotion, respectively, of dark-inducedleaf abscission was quantified using cuttings of coleus (ColeusBlumei Benth.). A continuous photon flux of approximately 15nM m^–2 s^–1 of red light was sufficient to preventleaf abscission. Abscission was promoted by exposure to a photonflux of approximately 10 nM m^–2 s^–1 of far-red lightThe inhibition of abscission by red light could be reversedby treatment with far-red and the promotion of abscission byfar-red light could be reversed by treatment with red lightThe data were consistent with a phytochrome receptor systemlocated in the leaves that controlled the presence of an abscission-inhibitingsubstance in the abscission zones. Key words: Abscission, Coleus Blumei, far-red light red light     

White light requirements for stimulation of plant growth by malformin

Over a 3-day period, the minimum white fluorescent light intensity required for malformin-induced growth stimulation of etiolated and green cuttings of Phaseolus aureus was approximately 2.6 × 10³ and 0.4 × 10³ ergs/cm² · sec, respectively. High light intensities were unable to inhibit the ability of malformin to stimulate growth. Over 3 days, the minimum photoperiod for malformin-induced growth stimulation using etiolated and green cuttings and a light intensity of 13.5 × 10³ ergs/cm² · sec was 4 hours and 1 hour, respectively. Malformin must be present in the area of growth stimulation during the time of light treatment. Those changes induced by light and required for malformin-induced growth stimulation were estimated to undergo almost complete decay within 1 hour in the dark. By manipulating the experimental technique, it was possible to stimulate the growth of green cuttings with malformin with a 10-min light treatment (13.5 × 10³ ergs/cm² · sec). Although low light intensities and short photoperiods did not allow growth stimulation by malformin using etiolated cuttings, they prevented or alleviated growth inhibition induced by malformin in the dark.     

Abscission in Coleus: Light and Phytohormone Control

Light control of leaf abscission in Coleus (Coleus blumei Benthcv. Ball 2719 Red) appears to be regulated by the quantity ofendogenous auxin transported from the leaf blade to the abscissionzone. Gas chromatographic—mass spectrophotometric analysisindicated that diffusate collected from leaf tissue treatedwith red light contained significantly higher levels of auxinthan dark and far-red light-treated leaf tissue. In addition,diffusate from red light-treated tissue inhibited abscissionof leafless petioles while diffusate from far-red light-treatedtissue promoted abcission when compared with diffusate fromdark-treated tissue. The effect of red light on abscission couldbe mimicked by IAA, but not by other phytohormones. An auxintransport inhibitor, 2, 3, 5-triiodobenzoic acid (TIBA), appliedeither as a lanolin ring around the petiole or vacuum infiltratedinto tissue, could completely eliminate any red light effecton abscission. The data are consistent with a phytochrome-mediatedlight regulation of endogenous auxin level in the leaf whichthen controls abscission. Key words: Abscission, Coleus, IAA, plant hormones, red (far-red) light, TIBA     

Light Requirement for AgNO(3) Inhibition of Ethrel-Induced Leaf Abscission from Cuttings of Vigna radiata

To obtain information regarding the antiethylene properties and binding site of Ag⁺, studies were initiated to define conditions under which Ag⁺ does or does not inhibit ethylene action. AgNO₃, applied as a leaf spray, inhibited 2-chloroethylphosphonic acid (Ethrel)-induced leaf abscission from green cuttings of Vigna radiata in white light but lost considerable activity in the dark. In the absence of Ethrel, AgNO₃ stimulated abscission in the dark. When cuttings were dark-aged for 24 hours prior to treatment with AgNO₃ and aged for an additional 24 hours in the dark after treatment, good inhibition of subsequent Ethrel-induced abscission was restored by returning the cuttings to light. However, when dark aging was preceded by far-red irradiation, considerably less inhibition of Ethrel-induced abscission was restored in the light. AgNO₃ was completely inactive on cuttings aged in the dark and treated with Ethrel in the dark. Light is required for the antiethylene activity of AgNO₃ with regard to leaf abscission of Vigna.     

Detection and Characterization of Abscission-Inhibiting Substances in Leaves of Malformin-Treated Cuttings

Malformin, which induces resistance to dark leaf abscissionfollowing treatment in the light, did not alter the course ofdark aging (loss of chlorophyll, wet and dry weight) in Vigna.Peroxydisulfate, which destroys IAA, did not influence malformininducedabscission resistance. Leaf blades from cuttings treated withmalformin in the light contained higher levels of abscissioninhibitors, which could be divided into ethanolsoluble and water-solublefractions. The inhibitors appeared to be heat stable anionsthat are insoluble in ether. Although malformin also increasedthe amount of abscission inhibitors in leaves when applied inthe dark, where malformin stimulates abscission, a parallelincrease in abscission stimulators may explain the failure ofthese inhibitors to function in the dark. (Received June 25, 1984; Accepted August 20, 1984)     

Mediation of a plant response to malformin by ethylene

Malformin and ethylene stimulate abscission of the primary leaves of Phaseolus aureus Roxb. in the dark, and abscission stimulation by both compounds is inhibited by indeleacetic acid and CO₂. Ethylene production by malformin-treated buds is stimulated within 4 hours. and up to 8 days, after treatment. Malformin-induced growth disturbances in P. vulgaris L. and abscission in P. aureus are considered mediated by ethylene. Although root curvatures of Zea mays L. are induced by both malformin and ethylene, and malformin is inhibited by CO₂, ethylene production is not stimulated by malformin. A role of ethylene in root curvatures induced by malformin is neither proposed nor disproved.     

Effect of Peroxydisulfate on Vigna radiata Abscission

K₂S₂O₈, applied to the basal end of cuttings of Vigna radiatastimulated leaf abscission in the light or dark. Because inhibitionof leaf sbscission in the dark by IAA was completely abolishedby K₂S₂O₈, and IAA decreased stimulation of abscission by K₂S₂O₈,destruction of IAA in the cuttings by K₂S₂O₈ is indicated. K₂S₂O₈had no effect on leaf abscission when applied as a foliar sprayor when roots of undisturbed seedlings were treated. When appliedproximally or distally to leafless explants, K₂S₂O₈ inhibitedpetiole abscission, and neither IAA nor ethylene had an effecton the inhibition. Although K₂S₂O₈ destroyed IAA in vitro, ithad no effect on abscission inhibitors in macerates of Vignaleaves and corn roots, nor did it destroy the biological activityof IAA added to such macerates. Substances liberated by macerationmay interfere with the ability of K₂S₂O₈ to destroy IAA. (Received May 2, 1981; Accepted August 24, 1981)     

An explanation for the light requirement of AgNO3 to inhibit ethylene-induced abscission

The loss of the antiethylene activity of Ag⁺ on leaf abscission by incubation in the dark was investigated. When primary leaves were removed from cuttings of Vigna radiata previously sprayed with AgNO₃, dark-induced abscission of the petioles was inhibited, compared to untreated leafless controls, in the presence or absence of ethephon, an ethylene-releasing compound. Malformin did not negate inhibition of petiole abscission induced by Ag⁺. Although leaf removal restored the antiethylene activity of Ag⁺ in the dark, macerates of leaves from dark-aged cuttings did not negate the ability of Ag⁺ to inhibit petiole abscission in the dark. Abscisic acid completely abolished the ability of Ag⁺ to counteract ethephon-induced leaf abscission in the light, and almost completely abolished the Ag⁺-induced inhibition of petiole abscission from explants in the dark. It is proposed that the phytochrome requirement for the antiethylene activity of Ag⁺ on ethephon-induced leaf abscission involves prevention of the formation, accumulation, or transport of a substance in leaves in the dark which negates Ag⁺ activity. This substance may be abscisic acid or another substance with similar biological activity.     

Induction of resistance to dark abscission by malformin in white light

When cuttings or seedlings of Phaseolus aureus were treated proximally with malformin for 2 days in continuous white light, resistance to subsequent leaf abscission in the dark resulted. The amount of resistance diminished as the concentration of malformin decreased from 10 to 0.1 micromolar. Resistance to dark abscission persisted for 7 days in continuous light. Little resistance was obtained when cuttings were taken from seedlings grown under low irradiance and short photoperiods, but resistance gradually increased as the photoperiod increased. Resistance to dark abscission induced by malformin in light differs from inhibition of abscission by indoleacetic acid because when malformin is applied in the dark it stimulates abscission after distal or proximal application. Malformin induces resistance only in conjunction with light treatment.     

Phytochrome involvement in stimulation and alleviation of inhibition of plant growth by malformin

Stimulation of stem elongation on green cuttings of Phaseolus aureus by malformin occurred only in red light and was specifically reversible by subsequent treatment with far red radiation. Inhibition of stem elongation of etiolated cuttings by malformin in the dark was alleviated by red light and was repeatedly reversible with far red irradiation. A direct or indirect effect of malformin on phytochrome action was suggested.     

Factors Influencing Adventitious Root Production in Cuttings of Griselinia littoralis and Griselinia lucida

Griselinia littoralis roots quickly and vigorously from cuttingsof seedlings and mature plants and also forms roots on detachedleaves. Cuttings root in the dark but leaves must be present.In contrast G. lucida roots vigorously only from cuttings takenfrom seedlings. Light is essential for root formation on oldermaterial. Detached leaves will not root. Although callus formationat the cut base commonly occurs in both species it is not directlyassociated with root formation. Griselinia littoralis Raoul Choix, Griselinia lucida Forst. f. Prodr., adventitious roots, stem cuttings, leaf cuttings, woody plants     

Effect of malformin on adventitious root formation and metabolism of indoleacetic acid-2-14C by Phaseolus vulgaris

Malformin inhibited rooting on cuttings of Phaseolus vulgaris.IAA antagonized malformin-induced inhibition of rooting, butmalformin inhibited IAA-induced swelling on the base of thecuttings. It was suggested that IAA-induced swelling was mediatedby ethylene. Malformin did not inhibit transport of root-promotingsubstances from upper portions of the cuttings or polar transportof IAA-2-¹⁴C, nor did it alter the melting point of DNA or thebinding of DNA to histone. Although malformin appeared to alterthe metabolism of IAA-2-¹⁴C, the effect may have been the resultof a marked and selective stimulation of efflux of IAA-2-¹⁴Cmetabolites by malformin. Efflux of IAA or its metabolites maycontribute toward inhibition of rooting by malformin. ¹ Journal Paper No. 4688 of the Purdue Agricultural ExperimentStation. Supported in part by grant GB-7158 from the NationalScience Foundation. ² Present address: Botanisches Institut der Technischen UniversitätBraunschweig, 3300 Braunschweig, Humboldtstraße 1. (Received March 9, 1972; )     

Modes of control by the circadian oscillator and the hourglass mechanism of the activities of cytoplasmic and chloroplast glyceraldehyde 3-phosphate dehydrogenases in Lemna gibba G3

Two types of clocks, i.e., the circadian oscillator and thehourglass mechanism, which under continuous light and darknessrespectively control the mutually inverse temporal changes inthe activities of Cyt-NAD-GPD and Chl-NADP-GPD of Lemna gibbaG3, were studied. Both clocks controlled the apparent Km values,not the Vmax values, of the GPD reactions for their substrateand coenzymes. A red light pulse inserted 3 hr after the onsetof the dark period eliminated the sigmoidal changes in darkness,but evoked rhythmical changes which otherwise did not occurin continuous darkness. Thus, the photosynthetic rhythm, ifpresent, would not sustain the GPD rhythms. This effect of ared light pulse was not nullified by a subsequent far red lightpulse. A far red light pulse given at the 3rd hour of an extendeddark period made conspicuous the sigmoidal changes in activityof GPDs in the dark period, and its effect was nullified bya subsequent red light pulse, suggesting that phytochrome isinvolved in the hourglass mechanism. (Received September 26, 1978; )