Petiole elongation inRumex species during submergence and ethylene exposure: The relative contributions of cell division and cell expansion

Submergence ofRumex crispus L. andR. palustris Sm. stimulates elongation of the youngest petiole. InR. palustris this response can be mimicked partially by exposure to exogenous ethylene. In both species, petiole elongation induced by ethylene and/or submergence is distributed nearly equally over the whole petiole length and is almost completely attributable to increased cell expansion. InR. acetosa L., extension of the youngest petiole is inhibited by submergence of the whole plant. The strongest growth inhibition within the youngest petiole was observed in the most distal parts and is probably the result of reduced cell expansion.     

Contrasting interactions between ethylene and abscisic acid in Rumex species differing in submergence tolerance

Complete submergence of flooding-tolerant Rumex palustris plants strongly stimulates petiole elongation. This escape response is initiated by the accumulation of ethylene inside the submerged tissue. In contrast, petioles of flooding-intolerant Rumex acetosa do not increase their elongation rate under water even though ethylene also accumulates when they are submerged. Abscisic acid (ABA) was found to be a negative regulator of enhanced petiole growth in both species. In R. palustris, accumulated ethylene stimulated elongation by inhibiting biosynthesis of ABA via a reduction of RpNCED expression and enhancing degradation of ABA to phaseic acid. Externally applied ABA inhibited petiole elongation and prevented the upregulation of gibberellin A(1) normally found in submerged R. palustris. In R. acetosa submergence did not stimulate petiole elongation nor did it depress levels of ABA. However, if ABA concentrations in R. acetosa were first artificially reduced, submergence (but not ethylene) was then able to enhance petiole elongation strongly. This result suggests that in Rumex a decrease in ABA is a prerequisite for ethylene and other stimuli to promote elongation.     

Is elongation-induced leaf emergence beneficial for submerged Rumex species?

Background and Aims

Plant species from various taxa ‘escape’ from low oxygen conditions associated with submergence by a suite of traits collectively called the low oxygen escape syndrome (LOES). The expression of these traits is associated with costs and benefits. Thus far, remarkably few studies have dealt with the expected benefits of the LOES.

Methods

Young plants were fully submerged at initial depths of 450 mm (deep) or 150–240 mm (shallow). Rumex palustris leaf tips emerged from the shallow flooding within a few days, whereas a slight lowering of shallow flooding was required to expose R. acetosa leaf tips to the atmosphere. Shoot biomass and petiole porosity were measured for all species, and treatments and data from the deep and shallow submergence treatments were compared with non-flooded controls.

Key Results

R. palustris is characterized by submergence-induced enhanced petiole elongation. R. acetosa lacked this growth response. Upon leaf tip emergence, R. palustris increased its biomass, whereas R. acetosa did not. Furthermore, petiole porosity in R. palustris was twice as high as in R. acetosa.

Conclusions

Leaf emergence restores gas exchange between roots and the atmosphere in R. palustris. This occurs to a much lesser extent in R. acetosa and is attributable to its lower petiole porosity and therefore limited internal gas transport. Leaf emergence resulting from fast petiole elongation appears to benefit biomass accumulation if these plants contain sufficient aerenchyma in petioles and roots to facilitate internal gas exchange.Key words: Submergence, emergence, enhanced shoot elongation, porosity, aerenchyma, Rumex, cost–benefit analysis, phenotypic plasticity     

Petiole elongation inRumex species during submergence and ethylene exposure: The relative contributions of cell division and cell expansion

Submergence ofRumex crispus L. andR. palustris Sm. stimulates elongation of the youngest petiole. InR. palustris this response can be mimicked partially by exposure to exogenous ethylene. In both species, petiole elongation induced by ethylene and/or submergence is distributed nearly equally over the whole petiole length and is almost completely attributable to increased cell expansion. InR. acetosa L., extension of the youngest petiole is inhibited by submergence of the whole plant. The strongest growth inhibition within the youngest petiole was observed in the most distal parts and is probably the result of reduced cell expansion.     

Sensitivity to ethylene: the key factor in submergence-induced shoot elongation of Rumex

Rosettes of flooding-resistant Rumex palustris plants show a submergence-induced stimulation of elongation, which is confined to the petioles of young leaves. This response increases the probability of survival. It is induced by ethylene that accumulates in submerged tissues. Flooding-intolerant Rumex acetosella plants do not show this response. We investigated whether differences in shoot elongation between the species, between old and young leaves and between the petiole and leaf blade of a R. palustris plant result from differences in internal ethylene concentration or in sensitivity to the gas. Concentrations of free and conjugated ACC in petioles and leaf blades of R. palustris indicated that ethylene is synthesized throughout the submerged shoot, although production rates varied locally. Nevertheless, no differences in ethylene concentration were found between submerged leaves of various ages. In contrast, dose-response curves showed that only elongation of young petioles of R. palustris was sensitive to ethylene. In R. acetosella, elongation of all leaves was insensitive to ethylene. We conclude that variation in ethylene sensitivity rather than content explains the differences in submergence-induced shoot elongation between the two Rumex species and between leaves of R. palustris.     

Ethylene Sensitivity and Response Sensor Expression in Petioles of Rumex Species at Low O2 and High CO2 Concentrations

Rumex palustris, a flooding-tolerant plant, elongates its petioles in response to complete submergence. This response can be partly mimicked by enhanced ethylene levels and low O2 concentrations. High levels of CO2 do not markedly affect petiole elongation in R. palustris. Experiments with ethylene synthesis and action inhibitors demonstrate that treatment with low O2 concentrations enhances petiole extension by shifting sensitivity to ethylene without changing the rate of ethylene production. The expression level of the R. palustris gene coding for the putative ethylene receptor (RP-ERS1) is up-regulated by 3% O2 and increases after 20 min of exposure to a low concentration of O2, thus preceding the first significant increase in elongation observable after 40 to 50 min. In the flooding-sensitive species Rumex acetosa, submergence results in a different response pattern: petiole growth of the submerged plants is the same as for control plants. Exposure of R. acetosa to enhanced ethylene levels strongly inhibits petiole growth. This inhibitory effect of ethylene on R. acetosa can be reduced by both low levels of O2 and/or high concentrations of CO2.     

The contrasting role of auxin in submergence-induced petiole elongation in two species from frequently flooded wetlands

The involvement of auxin in the submergence-induced petiole elongation has been investigated in Rumex palustris and Ranunculus sceleratus. Both wetland species are capable of enhanced petiole elongation upon submergence or treatment with exogenous ethylene (5μl l⁻¹). Treatment of intact Rumex palustris plants with 1-naphthalene acetic acid (NAA) at 10⁻⁴ M enhanced petiole elongation, while treatment with N -1-naphthylphthalamic acid (NPA) had no effect on petiole elongation. The elongation response after NAA or NPA treatment was comparable for plants in both submerged and drained conditions. Pre-ageing of detached petioles of Rumex palustris for 3 h in light or in dark conditions had no effect on the submergence-induced elongation. In comparison to intact plants, detached petioles of Rumex palustris , with or without lamina, did not show significant differences in responsiveness to IAA between drained or submerged conditions. This was in contrast to Ranunculus sceleratus where submergence caused a clear increase in responsiveness towards IAA. Removal of the lamina, the putative source of auxin, or treatment with NPA did not hinder the submergence-induced elongation of detached Rumex palustris petioles, but severely inhibited elongation of detached Ranunculus sceleratus petioles. This inhibition could be restored by application of NAA, suggesting the specific involvement of auxin in the submergence response of Ranunculus sceleratus. It is concluded that, in contrast to Ranunculus sceleratus , auxin is probably not involved in the submergence-induced petiole elongation of Rumex palustris.     

A kinetic analysis of hyponastic growth and petiole elongation upon ethylene exposure in Rumex palustris

Background and Aims

Complete submergence is an important stress factor for many terrestrial plants, and a limited number of species have evolved mechanisms to deal with these conditions. Rumex palustris is one such species and manages to outgrow the water, and thus restore contact with the atmosphere, through upward leaf growth (hyponasty) followed by strongly enhanced petiole elongation. These responses are initiated by the gaseous plant hormone ethylene, which accumulates inside plants due to physical entrapment. This study aimed to investigate the kinetics of ethylene-induced leaf hyponasty and petiole elongation.

Methods

Leaf hyponasty and petiole elongation was studied using a computerized digital camera set-up followed by image analyses. Linear variable displacement transducers were used for fine resolution monitoring and measurement of petiole growth rates.

Key Results

We show that submergence-induced hyponastic growth and petiole elongation in R. palustris can be mimicked by exposing plants to ethylene. The petiole elongation response to ethylene is shown to depend on the initial angle of the petiole. When petiole angles were artificially kept at 0°, rather than the natural angle of 35°, ethylene could not induce enhanced petiole elongation. This is very similar to submergence studies and confirms the idea that there are endogenous, angle-dependent signals that influence the petiole elongation response to ethylene.

Conclusions

Our data suggest that submergence and ethylene-induced hyponastic growth and enhanced petiole elongation responses in R. palustris are largely similar. However, there are some differences that may relate to the complexity of the submergence treatment as compared with an ethylene treatment.     

Growth responses of Rumex species in relation to submergence and ethylene

Abstract. Submergence stimulates growth of the petioles of Rumex palustris and Rumex crispus under field, greenhouse and laboratory conditions. Growth of Rumex acetosa petioles was hardly influenced by submergence. These growth responses under flooded conditions can be partially mimicked by exposing non-submerged Rumex plants to ethylene-air mixtures. Submergence of intact plants in a solution of AgNO₃ inhibited the elongation of all petioles of R. palustris and the youngest petiole of R. crispus and stimulated growth of the youngest petiole of R. acetosa , The ethylene-air mixture experiments, the effect of AgNO₃ and observed increase of the endogenous ethylene concentration during submergence suggest that ethylene plays a regulatory role in the growth responses of these Rumex species under submerged conditions. The three Rumex species showed a gradient in elongation responses to submergence, which correlates with the field distribution of the three species in a flooding gradient.     

Thermo- and Photoperiodicity and Involvement of Gibberellins during Day and Night Cycle on Elongation Growth of Begonia x hiemalis Fotsch

The effects of thermo- and photoperiodicity on elongation growth and on endogenous level of gibberellins (GAs) in Begonia x hiemalis during various phases of the day-night cycle have been studied. Plant tissue was harvested during the day and night cycle after temperature and photoperiodic treatments and analyzed for endogenous GAs using combined gas chromatography and mass spectrometry. Elongation growth increased when the difference between day and night temperature (DIF = DT − NT) increased from a negative value (−9.0 and −4.5°C) to zero and with increasing photoperiod from 8 to 16 h. When applied to the youngest apical leaf, gibberellins A₁, A₄, and A₉ increased the elongation of internodes and petioles. GA₄ had a stronger effect on elongation growth than GA₁ and GA₉. In relative values, the effect of these GAs decreased when DIF increased from −9 to 0°C. The time of applying the GAs during a day and night cycle had no effect on the growth responses. In general, endogenous levels of GA₁₉ and GA₂₀ were higher under negative DIF compared with zero DIF. The level of endogenous GA₁ in short day (SD)-grown plants was higher under zero DIF than under negative DIF, but this relationship did not appear in long day (LD)-grown plants. The main effects of photoperiod seem to be a higher level of GA₁₉ and GA₁ at SD compared with LD, whereas GA₂₀ and GA₉ show the opposite response to photoperiod. No significant differences in endogenous level of GA₁, GA₉, GA₁₉, and GA₂₀ were found for various time points during the diurnal day and night cycle. Endogenous GA₂₀ was higher in petiole and leaf compared with stem, whereas there were no differences of GA₁, GA₉, and GA₁₉ between plant parts. No clear relationship was found between elongation of internodes and petioles and levels of endogenous GAs. Received December 26 1996; accepted July 1, 1997     

Gibberellin Signal Transduction in Rice

Rumex acetosa L. (common sorrel) is a dioecious perennial in the family Polygonaceae. Gibberellins (GAs) of the early 13-hydroxylation pathway and the putative early 3, 13-hydroxylation pathway were previously identified in young R. acetosa inflorescences by GC-MS. In this investigation to examine the GA content of individual inflorescences ELISAs were used for quantitative analysis. Significant differences were revealed between the sexes in the GA content of young inflorescences, and GC-SRM was used to validate the observed trends. Males had higher levels of the 3, 13-hydroxylated C₂₀-GA GA₁₈ and the 2, 13-hydroxylated C₁₉-GA GA₂₉, whereas females had higher levels of the 13-hydroxylated C₂₀-GAs GA₅₃ and GA₁₉. It is suggested that the conversion from C₂₀-GAs to C₁₉-GAs is under tighter control in the inflorescences of females compared to male plants and therefore there is accumulation of the C₂₀-GAs in the females. Results from flowering bioassays using authentic GAs indicate that differences in GA content between the sexes are unlikely to be a consequence of sex determination.     

Light intensity, gibberellin content and the resolution of shoot growth in Brassica

The role of gibberellins (GAs) in the regulation of shoot elongation is well established but the phytohormonal control of dry-matter production is poorly understood. In the present study, shoot elongation and dry-matter production were resolved by growing Brassica napus L. seedlings under five light intensities (photon flux densities) ranging from 25 to 500 μmol m⁻² s⁻¹. Under low light, plants were tall but produced little dry weight; as light intensity was increased, plants were progressively shorter but had increasing dry weights. Endogenous GAs in stems of 16- and 17-d-old plants were analyzed by gas chromatography-selected ion monitoring with [²H₂] internal standards. The contents of GAs increased dramatically with decreasing light intensity: GA₁, GA₃, GA₈ and GA₂₀ were 62, 15, 16 and 32 times higher, respectively, under the lowest versus highest light intensities. Gibberellin A₁₉ was not measured at 25 μmol m⁻² s⁻¹ but was 9␣times greater in the 75 compared to 500 μmol m⁻² s⁻¹ treatment. Shoot and hypocotyl lengths were closely positively correlated with (log) GA concentration (for example: r ² = 0.93 for GA₁ and hypocotyl length) but shoot dry matter was negatively correlated with GA concentration. The application of gibberellic acid (GA₃) produced elongation of plants grown under high light, indication that their low level of endogenous GA was limiting shoot elongation. Although endogenous GA₂₀ showed the greatest influence of light treatment, metabolism of [³H]GA₂₀ and of [³H]GA₁ was only slightly influenced by light intensity, suggesting that neither 2β- nor 3β-hydroxylation were points of metabolic regulation. The results of this study indicate that GAs control shoot elongation but are not directly involved in the regulation of shoot dry weight in Brassica. The study also suggests a role of GAs in photomorphogenesis, serving as an intermediate between light condition and shoot elongation response. Received: 18 June 1998 / Accepted: 29 July 1998     

Narrow-band light regulation of ethylene and gibberellin levels in hydroponically-grown <Emphasis Type="Italic">Helianthus annuus</Emphasis> hypocotyls and roots

Both hypocotyl and root growth of sunflower (Helianthus annuus) were examined in response to a range of narrow-band width light treatments. Changes in two growth-regulating hormones, ethylene and gibberellins (GAs) were followed in an attempt to better understand the interaction of light and hormonal signaling in the growth of these two important plant organs. Hydroponically-grown 6-day-old sunflower seedlings had significantly elongated hypocotyls and primary roots when grown under far-red (FR) light produced by light emitting diodes (LEDs), compared to narrow-band red (R) and blue (B) light. However, hypocotyl and primary root lengths of seedlings given FR light were still shorter than was seen for dark-grown seedlings. Light treatment in general (compared to dark) increased lateral root formation and FR light induced massive lateral root formation, relative to treatment with R or B light. Levels of ethylene evolution (roots and hypocotyls) and concentrations of endogenous GAs (hypocotyls) were assessed from both 6-day-old sunflower plants either grown in the dark, or treated with FR, R or B light. Both R and B light had similar effects on hypocotyl and root growth as well as on ethylene and on hypocotyl GA levels. Dark treatment resulted in the highest ethylene levels, whereas FR treatment significantly reduced ethylene evolution for both hypocotyls and roots. R- and B-light treatments elevated ethylene evolution relative to FR light. Endogenous GA₅₃ and GA₁₉ levels in hypocotyls were significantly higher and GA₄₄, GA₂₀ and GA₁ levels significantly lower, for dark and FR light treatments compared to R and B light-treatments. The patterns seen for changes in GA concentrations indicate FR-, R- and B-light-mediated effects [differences] in the metabolism of the early C₂₀ GAs, GA₅₃ → GA₄₄ → GA_19. Surprisingly, GA₂₀, GA₁ and GA₈ levels in hypocotyls were very much reduced by treatment of the plants with FR light, relative to B and R-light treatments, e.g. the increased hypocotyl elongation induced by FR light was correlated with reduced levels of all three of the downstream C₁₉ GAs. The best explanation, albeit speculative, is that a more rapid metabolism, i.e. GA₂₀ → GA₁ → GA₈ → GA₈ conjugates occurs under FR light. Although this study provided no evidence that elevated ethylene evolution by roots or hypocotyls of sunflower is controlling growth via endogenous GA biosynthesis, there are differences between soil-grown and hydroponically-grown sunflower seedlings with regard to trends seen for hypocotyl GA concentrations and both root and hypocotyl ethylene evolution in response to narrow band width R and FR light signaling.     

Developing Inflorescences of Male and Female <Emphasis Type="Italic">Rumex acetosa</Emphasis> L. Show Differences in Gibberellin Content

Rumex acetosa L. (common sorrel) is a dioecious perennial in the family Polygonaceae. Gibberellins (GAs) of the early 13-hydroxylation pathway and the putative early 3, 13-hydroxylation pathway were previously identified in young R. acetosa inflorescences by GC-MS. In this investigation to examine the GA content of individual inflorescences ELISAs were used for quantitative analysis. Significant differences were revealed between the sexes in the GA content of young inflorescences, and GC-SRM was used to validate the observed trends. Males had higher levels of the 3, 13-hydroxylated C₂₀-GA GA₁₈ and the 2, 13-hydroxylated C₁₉-GA GA₂₉, whereas females had higher levels of the 13-hydroxylated C₂₀-GAs GA₅₃ and GA₁₉. It is suggested that the conversion from C₂₀-GAs to C₁₉-GAs is under tighter control in the inflorescences of females compared to male plants and therefore there is accumulation of the C₂₀-GAs in the females. Results from flowering bioassays using authentic GAs indicate that differences in GA content between the sexes are unlikely to be a consequence of sex determination.     

Gibberellin-ethylene interaction controls radial expansion in citrus roots

The involvement of gibberellins (GAs) and ethylene in the process of root radial expansion was studied in young seedlings of Carrizo citrange [Citrus sinensis (L.) Osb. × Poncirus trifoliata (L.) Raf.]. The GA inhibitors cycocel, paclobutrazol, and tetcyclacis enhanced radial expansion of the root tip (up to 2.3-fold) as a result of increases in stele diameter and inner cortex width. The GA deficiency increased cell number and width, and changed the polarity of growth, generating wider and shorter cortical cells in the elongation zone. In the presence or absence of GA inhibitors, GA₃ decreased root tip width and reduced all parameters related to radial expansion. The ethylene inhibitors (aminooxyacetic acid; cobalt ions, CoCl₂; silver thiosulfate) suppressed swelling induced by GA deficiency, generating thinner cells just as GA₃ did. In contrast to GA₃, ethylene inhibitors produced longer cells strongly resembling those of the untreated seedlings. Ethylene released by ethephon did not modify root tip width in control plants, while root diameter behind the root tip was increased. In the presence of low and ineffective concentrations of cycocel, the ethylene precursor 1-aminocyclopropane-1-carboxylic acid increased radial expansion of root tips (1.3-fold) and changed the polarity of growth, producing wider and shorter inner cortical cells as GA inhibitors did. These observations imply, first, that ethylene is the hormonal effector of the process of root radial expansion and, second, that the endogenous GAs modulate the promotive response of ethylene. Received: 4 October 1996 / Accepted: 25 December 1996     

Genomic fingerprinting of Frankia strains by PCR-based techniques. Assessment of a primer based on the sequence of 16S rRNA gene of Escherichia coli

Submergence stimulates elongation of the leaves of Rumex palustris and under laboratory conditions the maximum final leaf length (of plants up to 7 weeks old) was obtained within a 9 day period. This elongation response, mainly determined by petiole elongation, depends on the availability of storage compounds and developmental stage of a leaf. A starch accumulating tap root and mature leaves and petioles were found to supply elongating leaves with substrates for polysaccharide synthesis in expanding cell walls. Changes in the composition of cell wall polysaccharides of elongated petioles suggest a substantial cell wall metabolism during cell extension. Reduced starch levels or removal of mature leaves caused a substantial limitation of submerged leaf growth. From the 5th leaf onward enough reserves were available to perform submerged leaf growth from early developmental stages. Very young petioles had a limited capacity to elongate. In slightly older petioles submergence resulted in the longest final leaf lengths and these values gradually decreased when submergence was started at more mature developmental stages. Submerged leaf growth is mainly a matter of petiole elongation in which cell elongation has a concurrent synthesis of xylem elements in the vascular tissue. Mature petioles still elongated (when submerged) by cell and tissue elongation only: the annular tracheary elements stretched enabling up to 70% petiole elongation.     

The role of oxygen in submergence-induced petiole elongation in Rumex palustris: in situ measurements of oxygen in petioles of intact plants using micro-electrodes

In a study on the mechanism of stimulated petiole elongation in submerged plants, oxygen concentrations in petioles of the flood-tolerant plant Rumex palustris were measured with micro-electrodes. Short-term submergence lowered petiole partial oxygen pressure to c . 19 kPa whereas prolonged submergence under continuous illumination depressed oxygen levels to c . 8–12 kPa after 24 h. Oxygen levels in petioles depended on the presence of the lamina, even in submerged conditions, and on available light. In darkness, petiole oxygen levels in submerged plants dropped quickly to values as low as 0.5–4 kPa. It is hypothesized that prolonged submergence in the light is accompanied by a decrease in carbon dioxide in the petiole. Submergence-enhanced petiolar elongation rate was compared with emergent plants. Peak daily elongation rates occurred at the end of the dark period in emergent plants, but in the middle of the light period in submerged plants. We suggest that this shift in daily elongation pattern is induced by dependence of growth on photosynthetically derived oxygen in submerged plants. Implications of reduced oxygen for ethylene production are raised. Levels of 1- aminocyclopropane-1-carboxylic acid synthase and 1-aminocyclopropane-1-carboxylic acid oxidase and ethylene sensitivity are cited as potential factors in hypoxia-induced ethylene release.     

The role of gibberellins A1 and A3 in fruit growth of Pisum sativum L. and the identification of gibberellins A4 and A7 in young seeds

Gibberellins A₁ and A₃ are the major physiologically active gibberellins (GAs) present in young fruit of pea (Pisum sativum L.). The relative importance of these GAs in controlling fruit growth and their biosynthetic origins were investigated in cv. Alaska. In addition, the non-13-hydroxylated active GAs, GA₄ and GA₇, were identified for the first time in young seeds harvested 4 d after anthesis, although they are minor components and are not expected to play major physiological roles. The GA₁ content is maximal in seeds and pods at 6 d after anthesis, the time of highest growth-rate of the pod (Garcia-Martinez et al. 1991, Planta 184: 53–60), whereas gibberellic acid (GA₃), which is present at high levels in seeds 4–8 d after anthesis, has very low abundance in pods. Gibberellins A₁₉, A₂₀ and A₂₉ are most concentrated in seeds at, or shortly after, anthesis and their abundance declines rapidly with development, concomitant with the sharp increase in GA₁ and GA₃ content. Application of GA₁ or GA₃ to the leaf subtending an emasculated flower stimulated parthenocarpic fruit development. Measurement of the GA content of the pods at 4 d after anthesis indicated that only 0.002–0.5% of the applied GA was transported to the fruit, depending on dose. There was a linear relationship between GA₁ content and pod weight up to about 2 ng · (g FW)⁻¹, whereas no such correlation existed for GA₃ content. The concentration of endogenous GA₁ in pods from pollinated ovaries is just sufficient to give the maximum growth response. It is concluded that GA₁, but not GA₃, controls pod growth in pea; GA₃ may be involved in early seed development. The distribution of GAs within the seeds at 4 d post anthesis was also investigated. Most of the GA₁, GA₈, GA₁₉, GA₂₀ and GA₂₉ was present in the testa, whereas GA₃ was distributed equally between testa and endosperm and GA₄ was localised mainly in the endosperm. Of the GAs analysed, only GA₃ and GA₂₀ were detected in the embryo. Metabolism experiments with intact tissues and cell-free fractions indicated compartmentation of GA biosynthesis within the seed. Using ¹⁴C-labelled GA₁₂, GA₉, 2,3-didehydroGA₉ and GA₂₀ as substrates, the testa was shown to contain 13-hydroxylase and 20-oxidase activities, the endosperm, 3β-hydroxylase and 20-oxidase activities. Both tissues also produced 16,17-dihydrodiols. However, GA₁ and GA₃ were not obtained as products and it is unlikely that they are formed via the early 13-hydroxylation pathway. [¹⁴C]gibberellin A₁₂, applied to the inside surface of pods in situ, was metabolised to GA₁₉, GA₂₀, GA₂₉, GA₂₉-catabolite, GA₈₁ and GA₉₇, but GA₁ was not detected. Gibberellin A₂₀ was metabolised by this tissue to GA₂₉ and GA₂₉-catabolite. Received: 23 July 1996 / Accepted: 2 September 1996