An Endogenous 24-hour Rhythm in the Growth Rate of the Avena Coleoptile

The rates of growth of coleoptiles of intact Avena seedlingswere studied by means of time-lapse photography, using infra-redradiation. When the seedlings are germinated in red light and subsequentlytransferred to darkness, a growth rhythm is established in whichthe first peak in the growth-rate curve occurs about 16–17hours after the transfer, and the second peak 24 hours later.When the transfer is made sufficiently early, three peaks mayoccur before growth ceases. The occurrence of the peaks andthe emergence of the primary leaf are independent of one another. Alteration of the point in the life-history at which the seedlingsare transferred from light to darkness changes the times ofoccurrence of the peaks, but does not affect the period of therhythm. The incidence of the rhythm shows no correlation withtime of day; therefore the rhythm is not due to diurnal changesin external conditions. Interruption of the dark period by several hours' exposure tored light causes the suppression of a previously induced rhythmand the establishment of a new one which commences at the timethe seedlings are restored to darkness. When they are grownunder continuous red light no rhythm is induced. Within the range 16 to 28 C., temperature has little or noeffect on the period of the rhythm. When seedlings of Triticum are grown under the same conditionsas those which induce a rhythm in Avena, no rhythmical variationin the growth rate can be detected.     

The Effects of Indole-3-Acetic Acid and 2:4-Dichlorophenoxyacetic Acid on the Growth Rate and Endogenous Rhythm of Intact AvenaColeoptiles

The rates of elongation of the coleoptiles of Avena seedlings,subjected to intermittent immersion in solutions of IAA or 2:4-Dfor various total periods, were determined from measurementsof photographs taken every hour by infra-red radiation. Immersion in 17·5 mg./l. IAA for 1–5 hours causeda large increase in the growth rate followed by a depression.When the seedlings were immersed in 8·75 mg./l. IAA forperiods of 12 or 24 hours the depression was partially overcomeso long as the treatment was continued. Absorption of additionalIAA by the coleoptiles reduced their geotropic sensitivity. Penetration of 2:4-D (sodium salt) into the coleoptiles wasslower than that of IAA and the resulting stimulation of thegrowth rate was less, particularly in unbuffered solutions.After the treatment the growth rate declined slowly to aboutthe normal value. Results with coleoptiles were very similar to those previouslyobtained with rhizomes of Aegopodium and suggest that inhibitionof growth following stimulation by IAA may be of general occurrence.Possible causes of the inhibition are discussed and a comparisonis made between the results with intact coleoptiles and observationsmade by others on coleoptile sections. Temporary immersion of the seedlings in auxin solutions depressedthe rate of elongation of the primary leaf while it increasedthat of the coleoptile. It caused little disturbance of theendogenous rhythm induced by change from light to darkness.The suggestion that such rhythms can be explained in terms ofvariation in concentration of IAA-oxidase is not supported.     

The Occurrence of Endogenous Rhythms in the Coleoptiles in Various Cereal Genera

The rate of growth of the coleoptiles was determined from photographstaken by infra-red radiation. CO₂ output was measured by meansof an infra-red gas analyser. The rhythm of CO₂ output from the coleoptile of Avena was inducedby a change from red light to darkness. It has a period of about24 hours and agrees in timing with the growth-rate rhythm previouslyrecorded. Some degree of rhythmicity in the growth-rate was found in Triticumvulgare (var. ‘Eclipse’) and in Secale cereale (var.Petkus). Very slight indications of rhythmicity were found inTriticum spelta and in Hordeum vulgare. Negative results wereobtained with Oryza sativa and with Zea mays. Where rhythmicityin the coleoptile is less strongly developed, the peaks comecloser together, the interval being about 18–20 hours.Cereals cannot be sharply separated into two groups accordingto the presence or absence of rhythmicity in the coleoptile.Of the genera examined, the most marked endogenous rhythms occurin Avena. It is doubtful if the ability of the coleoptile toexhibit an endogenous rhythm has any beneficial effect on thedevelopment of the seedling. Under normal conditions of germinationinduction of the rhythm would not occur.     

The Effects of Decapitation, Lack of Oxygen, and Low Temperature on the Endogenous 24-hour Rhythm in the Growth-rate of the Avena Coleoptile

Further work on the endogenous rhythm in the growth-rate ofthe Avena coleoptile was carried out by the methods previouslydescribed. Decapitation of the coleoptile does not prevent induction ofthe rhythm, nor does it affect the phase of a rhythm previouslyestablished. When seedlings are transferred to darkness and are simultaneouslydeprived of oxygen by replacing the surrounding air with nitrogen,a rhythm is induced, but the first peak is delayed for a periodapproximately equal to that of the nitrogen treatment. Providedthe period in nitrogen is not excessively prolonged, the retardationof the second peak is less than that of the first. This suggeststhat the rate of the time-keeping mechanism has become accelerated.Since only a part of the initial retardation in the rhythm isthus eliminated, a change in phase persists. The younger theseedlings at the time of treatment, the smaller is this persistentchange. When the nitrogen treatment is commenced some hoursafter the transfer to darkness, the retardation of the secondpeak is greater than when treatment and transfer are simultaneous.In each series the retardation increases exponentially as thelength of the period in nitrogen is extended. Retardation followedby acceleration was also observed after the seedlings had beenexposed to low temperature. It seems probable that induction of the rhythm involves thesynchronization of independent time-keeping mechanisms alreadyin existence, rather than the establishment of an entirely newsystem.     

IAA transport during the phototropic responses of intact Zea and Avena coleoptiles

Summary Transport of indolyl-3-acetic acid (IAA) was studied during the phototropic responses of intact shoots and detached coleoptiles of Zea mays L. and Avena sativa L. The use of a high specific activity [5-³H]IAA and glass micropipettes enabled asymmetric application of the IAA to be made to individual coleoptiles with minimal tissue damage.A unilateral stimulus of 2.59×10^-11 einstein cm^-2 of blue light, probably in the dose range of the first positive phototropic response, caused significant net lateral movement of radioactivity from [5-³H]IAA away from the illuminated side of intact shoots and detached coleoptile apices of both Avena and Zea. The magnitude of the net lateral movement was 15.3% in Zea seedlings and 12.3% in Avena seedlings. Chromatographic analyses indicated that the movement of radioactivity reflected that of IAA. A phototropic stimulus of 1.24×10^-7 einstein cm^-2, which was probably in the second positive dose range, caused significant lateral movement of radioactivity in intact shoots and detached coleoptiles of Zea but not of Avena.In intact Zea seedlings, neither phototropic dosage affected the longitudinal transport of IAA. In intact Avena seedlings, first positive stimulation inhibited longitudinal transport only when the IAA was applied to the illuminated side of the coleoptile, but second positive stimulation inhibited basipetal movement of IAA regardless of the side of application.Exposing the intact seedlings to red light before phototropic stimulation abolished lateral transport after a first positive stimulus in Zea and in Avena.Phototropic stimulation can thus induce a lateral transport of IAA towards the shaded side of the coleoptiles of both Zea and Avena seedlings, and can affect longitudinal movement of IAA in the coleoptile of Avena. However, since phototropic curvature was observed under certain conditions in the absence of either of these effects, the extent to which they are involved in the induction of asymmetric growth in a stimulated coleoptile has yet to be resolved.     

Physiological activity of a viridicatin derivative, 3-(4-phenylcarbostyriloxy) acetic acid

A carboxymethylene derivative (V-OCH₂COOH) of viridicatin (V-OH)promoted the root growth of rice and sesame seedlings. V-OCH₂COOHhad no known hormonal activities, per se, but did have an inhibitoryeffect on IAA and 2,4-D-induced growth of Avena coleoptile sectionsand of carrot root callus. However, inhibition by VOCH2COOHof 2,4-D-induced growth in carrot root callus was to some extentreversed by increasing the concentration of 2,4-D. V-OCH₂C0OHseemed to competitively inhibit IAA-induced elongation of Avenacoleoptile sections. (Received September 14, 1970; )     

Some Responses of Avena Coleoptiles to Ethylene

Ethylene pretreatment of intact Avena seedlings or of excisedcoleoptile sections results in an increased response of thecells to auxin. It is suggested that ethylene brings about theacceleration of hydrolytic reactions controlling the physicalproperties of cell walls and hence increases their capacityfor growth. Coleoptile elongation of intact seedlings is inhibitedby ethylene; this inhibition is concurrent with a lateral expansionof the entire coleoptile. It is suggested that under a givenset of conditions coleoptile cells are capable of attaininga finite volume and that the preferential lateral expansioninduced by ethylene is accomplished at the expense of longitudinalextension. Experiments with intact and deseeded plants indicatethat lateral expansion depends on the supply of some factorfrom the endosperm.     

Effect of Peeling on IAA-induced Growth in Avena Coleoptiles

The act of peeling removes the epidermis exclusively from Avenacoleoptiles. Peeling inhibits IAA-induced growth, by inhibitingthe growth of segments incubated in the presence of IAA, andpromoting that of those incubated in water. The magnitude ofthe inhibition of IAA-induced growth is proportional to theamount of epidermis removed. It is shown that neither lateralswelling, wounding, anaerobiosis, nor exposure to supraoptimalconcentrations of IAA cause the inhibition. It is concludedthat in Avena coleoptiles the epidermis regulates the rate ofexpansion of the underlying parenchyma cells and is the principaltarget of IAA-action. Avena sativa L., oat, coleoptile, indol-3-ylacetic acid, auxin, extension growth     

The Growth-time Relationships of the Auxin- induced Growth in Avena Coleoptile Sections

1. 1. The growth rate of Avena coleoptile sections in the presenceof indoleacetic acid (IAA) is constant with time over a widerange of time intervals and IAA concentrations.
2. 2. Constancyof growth rate is dependent upon the maintenanceof constantconditions in which the concentration of IAA availableto thesection remains the chief factor limiting growth rate.
3. 3.Control of the pH of the medium in which the sections aregrownis essential to the maintenance of constant growth rate,particularlyin the presence of high concentrations of IAA.
4. 4. The lagperiod in establishment of steady growth rate bysections inthe presence of IAA is less than 10 minutes andis not detectableby present methods of measurement.

     

The Effect of High Concentrations of Auxin on the Extension of Avena Coleoptile Sections

The response of Avena coleoptile sections to high concentrationsof auxin has been determined in the absence of all additivesexcept sucrose. In most experiments the growth-time curves with75 p.p.m. IAA showed two linear phases. In the first phase,which lasted for only 2–4 hours, extension was as rapidwith 75 p.p.m. IAA as with 5 p.p.m. IAA. This rapid initialexpansion phase was then succeeded by a second phase which persistedfor at least 20 hours. During this second linear phase the growth-ratewith 75 p.p.m. IAA was lower than with an auxin concentrationof 5 p.p.m. In some experiments the first phase was absent andonly the second phase was present. The response of sections to high concentrations of auxin wasnot influenced by the presence of buffers or absorbable cations.Omission of sucrose or the presence of moderate amounts of ethanolcaused the resulting growth curves to be non-linear. The rate of uptake of auxin into the tissues was dependent onthe auxin concentration and was constant for at least 24 hours.     

The Effects of Externally Applied 3-indolylacetic Acid on Phototropic Induction and Response in the Coleoptile of Avena

The effects of intermittent immersion of Avena seedlings insolutions of IAA on the response of the coleoptiles to unilateralillumination in the region of that producing the second positivecurvature were studied by means of automatic time-lapse photographywhich enabled the growth-rate and curvature to be recorded simultaneously. Phototropic induction occurred even after the coleoptiles hadabsorbed sufficient IAA from a 10^-4 M. solution to raise theirrate of elongation to about twice the normal value. Phototropiccurvature, which had been temporarily inhibited by a curvaturein the opposite direction induced by the IAA, became evidentas soon as this curvature had ceased to operate. In coleoptiles, supplied with IAA after the commencement ofa phototropic curvature, the response was temporarily suppressed.It was resumed as soon as the effects of the exogenous IAA haddisappeared. The ability of the coleoptiles to produce a slight phototropicresponse persisted even when their growth-rate had been greatlyreduced by previous removal of the endosperm. Increasing thegrowth-rate by supplying the starved seedlings with IAA or sucrose,separately or together, failed to increase the response. Decapitation did not prevent phototropic induction, but delayedthe onset of the response. Application of IAA by intermittentimmersion in a 0.1 mg./l. solution, after the decapitated coleoptileshad been exposed to unilateral illumination, increased the rateof growth but reduced the response. The results suggest that in these experiments phototropic inductionwas not mediated by any direct action of light on the displacement,inactivation, or rate of synthesis of an endogenous auxin. Theyare in agreement with the hypothesis that the stimulus causedan asymmetrical distribution of a co-factor of auxin.     

Short-Term Stimulation of Growth Induced by the Apical Application of IAA to Intact Maize Coleoptiles

Indole-3-acetic acid (IAA), mixed with lanolin, was appliedto the surface of defined parts of the intact coleoptile ofmaize (Zea mays L.) seedlings, and the elongation growth ofthe coleoptile zone was monitored for a period of 8 h. WhenIAA was applied to a subapical region, the growth of zones locatedbelow was stimulated only temporarily, although stimulationwas continuous when IAA was applied directly to the zone thatwas monitored for growth. This short-term stimulation was observedat all concentrations tested (0.03–30 mg of IAA per gof lanolin). The duration of stimulated growth, which variedfrom 1 to 5 h, was longer as the distance from the site of IAAapplication was reduced and the concentration of IAA was increased.Growth during the post-stimulation phase after application ofa high dose of IAA could not be enhanced again by applying IAAnear the site of the first application, but it was enhancedwhen IAA was applied directly to the zone used to measure growth.These results suggest that the supply of IAA from the site ofapplication to lower zones is controlled internally such thatthe elevated concentration of IAA in these zones returns tothe concentration before IAA application. Either the feedbackregulation of auxin transport or the feedforward regulationof auxin metabolism may account for the suggested control ofIAA supply. (Received May 18, 1995; Accepted October 20, 1995)     

Sources of Free IAA in the Mesocotyl of Etiolated Maize Seedlings

Sources of free indole-3-acetic acid (IAA) for the mesocotyl of intact etiolized maize ((Zea mays L.) seedlings are evaluated. The coleoptile unit, which includes the primary leaves and the coleoptilar node, is the main source of free IAA for the mesocotyl. The seed and the roots are not immediate sources of IAA supply. Dependence of the apical growing region of the mesocotyl on the coleoptile unit as a source of free IAA is almost total. One-half or more of the supply of IAA comes from the coleoptile tip, the rest mainly from the primary leaves. Removal of the coleoptile tip results in inhibition of mesocotyl elongation. The hypothesis that growth of the mesocotyl is regulated by auxin supplied by the coleoptile is supported. Conjugated forms of IAA appear to play little part in regulating the levels of free IAA in the shoot.     

Inhibitory action of red light on the growth of the maize mesocotyl: evaluation of the auxin hypothesis

Brief irradiation of 3-d-old maize (Zea mays L.) seedlings with red light (R; 180 J m^-2) inhibits elongation of the mesocotyl (70–80% inhibition in 8 h) and reduces its indole-3-acetic acid (IAA) content. The reduction in IAA content, apparent within a few hours, is the result of a reduction in the supply of IAA from the coleoptile unit (which includes the shoot apex and primary leaves). The fluence-response relationship for the inhibition of mesocotyl growth by R and far-red light closely resemble those for the reduction of the IAA supply from the coleoptile. The relationship between the concentration of IAA (1–10 M) supplied to the cut surface of the mesocotyl of seedlings with their coleoptile removed and the growth increment of the mesocotyl, measured after 4 h, is linear. The hypothesis that R inhibits mesocotyl growth mainly by reducing the IAA supply from the coleoptile is supported. However, mesocotyl growth in seedlings from which the coleoptiles have been removed is also inhibited by R (about 25% inhibition in 8 h). This inhibition is not related to changes in the IAA level, and not relieved by applied IAA. In intact seedlings, this effect may also participate in the inhibition of mesocotyl growth by R. Inhibition of cell division by R, whose mechanism is not known, will also result in reduced mesocotyl elongation especially in the long term (e.g. 24 h).Abbreviations FR far-red light - IAA indole-3-acetic acid - P_fr phytochrome in the far-red-absorbing form - P_r phytochrome in the red-absorbing form - R red light     

Growth Regulator Interactions in the Growth of the Shoot System of Avena sativa Seedling: II. THE GROWTH OF THE FIRST LEAF AND THE COLEOPTILE1

1. Studies have been made of the growth in culture medium of thecomponent parts of compositesegments excised from 3 to 7-day-oldAvena sativa seedlings and comprising portions of coleoptileand first leaf bases and various lengths of first internodetissue.
2. The effects of various concentrations of gibberellicacid (GA)and indole-3- acetic acid (IAA) alone and in combinationhavebeen studied on the growth of these organs.
3. Both GA andIAA stimulate the growth of coleoptile base tissuebut in combinationtheir joint effects are less than additive.No synergism occurs.
4. The growth of the first-leaf base is greatly stimulated byGAbut is inhibited by IAA. In combination, the stimulatoryeffectof GA (up to 1 0 p.p.m.) may be virtually eliminatedby evenlow concentrations of IAA (0.01 p.p.m.).
5. The inclusionof first internode tissue in the segments considerablyincreasesthe growth of first leaf base tissue but has no consistenteffecton the growth of coleoptile base tissue. The presenceof firstinternode tissue also greatly increases the degreeof growthstimulation invoked by GA but does not influence thedegreeof IAA inhibition. It is postulated that the first internodetissue is the source of an unknown growth factor necessary forGA action in the first leaf and potentiating the action of endogenousgibberellin.
6. Kinetin, adenine sulphate, glutarnine, glutarnicacid, asparagine,glycine, arginine, histidine, lysine, aneurin,and pyridoxinewill not simulate the effects of this unknowngrowth factorin the growth of leaf tissue. Like IAA, kinetinvirtually eliminatesthe GA stimulation of leaf growth.
7. Astudy of extracts of internode tissue in various solvents,analysedby paper partition chromatography and assayed by thegrowthof the first leaf base, has indicated the presence ofgrowthinhibitors and gibberellin-like substances but has failedtoisolate the postulated endogenous GA-synergist.
8. The implicationsof these results for growth correlations andthe hormone controlof shoot growth in Avena sativa seedlingsis discussed.

     

Bound indoleacetic Acid in Avena coleoptiles

When C¹⁴ carboxyl indoleacetic acid (IAA) is transported through Avena coleoptile sections a fraction of the activity becomes bound. The nature of this bound IAA has been investigated. Upon extraction with solvents and chromatography a substance having the R_F of IAA in 4 solvents was detected. No evidence could be found for the formation of indoleacetyl conjugates. In pea stem sections subjected to a similar experimental regime good evidence was obtained for the occurrence of conjugates. When IAA was supplied exogenously to coleoptile sections floating in solutions the occurrence of conjugates was shown to be dependent on the presence of the primary leaf. In its absence no conjugates could be detected.

On grinding coleoptile sections and subsequent centrifugation at 240 × g the radioactivity was found to be in the tissue fraction as opposed to the supernatant. The radioactivity cannot be removed from the tissue by extraction with water, buffer solution or treatment with ribonuclease. It is readily removed by 10% urea, crystalline trypsin and chymotrypsin. It is therefore concluded that IAA becomes bound to a protein. Bound IAA does not appear to be able to cause growth in Avena coleoptile sections.

     

The lateral transport of IAA in intact coleoptiles of Avena sativa L. and Zea mays L. during geotropic stimulation

Summary Movement of IAA was studied in excised coleoptile apices and whole seedlings of Zea mays L. and Avena sativa L. during geotropic stimulation. A micropipette technique permitted the application of [5-³H]IAA at predetermined points on the coleoptiles with minimal tissue damage.When [5-³H]IAA was applied to the upper side of a horizontal excised Zea coleoptile, about 60% of the recoverable radioactivity had moved into the lower half after 2 h. In contrast, when application was made to the lower side of a horizontal excised coleoptile, only 4% of the radioactivity migrated to the upper half. There was, thus, a net downward movement of 56%. Similar patterns of distribution were found for radioactivity in both the tissue and the basal receiver blocks. In horizontal shoot tissues of intact Zea seedlings a net downward movement of about 30% of the recoverable radioactivity occurred after 1 h of geotropic stimulation. Comparable experiments with Avena indicated a net downward movement of 6–12% in excised apices of coleoptiles and in the intact shoot. In both Zea and Avena chromatographic analyses of tissue and receiver blocks indicated that the movement of radioactivity reflected that of IAA.In Zea coleoptiles, the lateral migration of radioactivity after 2 h was 3 to 4 times greater in the apical tissues than in the basal tissues. A significant net downward movement of radioactivity was detected after 10 min of geotropic stimulation in the extreme apex of Zea coleoptiles but not in the more basal regions.These experiments show that downward lateral transport of IAA occurs in intact shoots of Zea and Avena seedlings upon geotropic stimulation. Lateral transport of IAA had previously been demonstrated only in sub-apical segments of Zea coleoptiles.     

A Critical Study of the Auxin Theory of Growth Regulation in the Mesocotyl of Avena sativa

A method of growing Avena seedlings is described, which allowsthem to be handled individually in darkness. Mesocotyls of seedlinge from which the tip of the coleoptileis repeatedly removed are as long as those of control plantsnot so decapitated. Mesocotyls of seedlings which are deseeded on the 3rd day ofgrowth, followed by decapitation of the cleoptile tip on the4th day, are, at 7 days old, as long as those of controls notso decapitated. When deseeded plants are decapitated, regeneration of auxinproduction occurs at the tip of the coleoptile stump. Where a reduction in the length of the mesocotyl results fromdecapitation, a wound reaction is probably concerned in additionto any auxin changes. Removal of the coleoptilar node causes a sharp decrease in thefinal length of the mesocotyl. Heating intact seedlings at 40° C. for 3 hours causes areduction in the length of the mesocotyl but not of the coleoptile.The effect of heating is not reversed by subsequent treatmentat low temperature, which instead appears to augment these effects. When seedlings are exposed to the action of KCN, iodoacetate,or anaerobic conditions, and illuminated while so exposed, perceptionof light takes place, resulting in a reduction in the lengthof the mesocotyl. Perception of light takes place in seedlings germinated at normaltemperatures, but maintained at low temprature during illuminationand also in seedlings grown for 6 weeks at 2° C. withoutany previous growth at normal temperature. Light perception takes place in embryos excised from dry grainand grown on a culture medium. No difference in free amino-acid content is apparent betweendark grown and illuminated seedlings. The effects of illumination survive a period of drying downand become apparent upon subsequent germination of the grainin darkness. The drying process itself causes an additionalreduction in mesocotyl length. It is concluded that auxin itself is not the primary reactantin the perception process, and that the growth of the mesocotylis probably controlled by the coleoptilar node and plumulargrowing point, rather than by auxin diffusing downward fromthe tip of the coleoptile.     

The Geoelectric Effect in Plant Shoots: III. DEPENDENCE UPON AUXIN CONCENTRATION GRADIENTS AND AEROBIC METABOLISM

The development of the geoelectric effect has been followedin Zea coleoptiles with a flowing-solution electrode system,and its dependence upon auxin concentration gradients and aerobicmetabolism assessed. A symmetrical source of IAA can effectively replace the coleoptiletip in allowing the geo-electric potential to occur. The diffusatefrom coleoptile tips, when applied asymmetrically to the apexof a vertical decapitated coleoptile, generates a potentialdifference across the coleoptile indistinguishable from thatinduced by the asymmetrical application of IAA. Asymmetricalapplication of IAA to vertical Avena and Zea coleoptiles andHelianthus hypocotyls induces closely similar responses. Neither the geoelectric effect nor a geotropic response developswhen intact Zea coleoptiles are placed horizontally after beingdeprived of oxygen, but they both occur when an aerobic atmosphereis restored. The lateral potential difference induced by theasymmetrical application of IAA to the apex of a vertical coleoptiledoes not occur under anoxic conditions. With a static-drop electrode system and a decapitated Zea coleoptile,a potential difference develops immediately after reorientationof the coleoptile into the horizontal position, and attainsa maximum value after about 10 min. This potential differencecan be further increased by the asymmetrical application ofIAA to the lower half of the apical cut surface of the coleoptile. Our data support the view that both the geoelectric potentialand the geotropic response are due to the IAA concentrationgradient which arises from the lateral transport of this substancefrom the upper to the lower half of the horizontal shoot. Theyalso bear out our previous conclusions that the ‘geoelectricpotential’ observed with static-drop electrodes and anintact shoot, is the resultant of two processes. The first isa physical phenomenon arising in the electrodes, or betweenthe electrodes and the plant tissue, and the second arises inthe living tissues of the shoot as the result of gravity-inducedchanges in auxin distribution.     

A growth inhibitor fromCastanea sativa Mill. cuttings

The effect on growth of an aliphatic acid isolated fromCastanea sativa cuttings was studied as well as its interaction with IAA. TheAvena coleoptile straight growth test was used. A growth inhibition was observed in a wide range of concentrations. The compound lowered or suppressed the IAA induced elongation of theAvena coleoptilo growth sections.