Pedicel Abscission Research Articles

Identification of defense-related genes newly-associated with tomato flower abscission

The current abscission model suggests the formation of a post-abscission trans-differentiation of a protective layer as the last step of the process. The present report expands the repertoire of genes activated in the tomato flower abscission zone (AZ), which are likely to be involved in defense responses. We identified four different defense-related genes, including: Cysteine-type endopeptidase, α-Dioxygenase 1 (α-DOX1), HopW-1-1-Interacting protein2 (WIN2), and Stomatal-derived factor-2 (SDF2), that are newly-associated with the late stage of the abscission process. The late expression of these genes, induced at 8-14 h after flower removal when pedicel abscission was already in progress, was AZ-specific, and was inhibited by treatments that prevented pedicel abscission, including 1-methylcyclopropene pretreatment or IAA application. This information supports the activation of different defense responses and strategies at the late abscission stages, which may enable efficient protection of the exposed tissue toward different environmental stresses.

Microarray Analysis of the Abscission-Related Transcriptome in the Tomato Flower Abscission Zone in Response to Auxin Depletion

The abscission process is initiated by changes in the auxin gradient across the abscission zone (AZ) and is triggered by ethylene. Although changes in gene expression have been correlated with the ethylene-mediated execution of abscission, there is almost no information on the molecular and biochemical basis of the increased AZ sensitivity to ethylene. We examined transcriptome changes in the tomato (Solanum lycopersicum 'Shiran 1335') flower AZ during the rapid acquisition of ethylene sensitivity following flower removal, which depletes the AZ from auxin, with or without preexposure to 1-methylcyclopropene or application of indole-3-acetic acid after flower removal. Microarray analysis using the Affymetrix Tomato GeneChip revealed changes in expression, occurring prior to and during pedicel abscission, of many genes with possible regulatory functions. They included a range of auxin- and ethylene-related transcription factors, other transcription factors and regulatory genes that are transiently induced early, 2 h after flower removal, and a set of novel AZ-specific genes. All gene expressions initiated by flower removal and leading to pedicel abscission were inhibited by indole-3-acetic acid application, while 1-methylcyclopropene pretreatment inhibited only the ethylene-induced expressions, including those induced by wound-associated ethylene signals. These results confirm our hypothesis that acquisition of ethylene sensitivity in the AZ is associated with altered expression of auxin-regulated genes resulting from auxin depletion. Our results shed light on the regulatory control of abscission at the molecular level and further expand our knowledge of auxin-ethylene cross talk during the initial controlling stages of the process.

Sequential cell wall transformations in response to the induction of a pedicel abscission event in Euphorbia pulcherrima (poinsettia)

Alterations in the detection of cell wall polysaccharides during an induced abscission event in the pedicel of Euphorbia pulcherrima (poinsettia) have been determined using monoclonal antibodies and Fourier transform infrared (FT-IR) microspectroscopy. Concurrent with the appearance of a morphologically distinct abscission zone (AZ) on day 5 after induction, a reduction in the detection of the LM5 (1-->4)-beta-D-galactan and LM6 (1-->5)-alpha-L-arabinan epitopes in AZ cell walls was observed. Prior to AZ activation, a loss of the (1-->4)-beta-D-galactan and (1-->5)-alpha-L-arabinan epitopes was detected in cell walls distal to the AZ, i.e. in the to-be-shed organ. The earliest detected change, on day 2 after induction, was a specific loss of the LM5 (1-->4)-beta-D-galactan epitope from epidermal cells distal to the region where the AZ would form. Such alteration in the cell walls was an early, pre-AZ activation event. An AZ-associated de-esterification of homogalacturonan (HG) was detected in the AZ and distal area on day 7 after induction. The FT-IR analysis indicated that lignin and xylan were abundant in the AZ and that lower levels of cellulose, arabinose and pectin were present. Xylan and xyloglucan epitopes were detected in the cell walls of both the AZ and also the primary cell walls of the distal region at a late stage of the abscission process, on day 7 after induction. These observations indicate that the induction of an abscission event results in a temporal sequence of cell wall modifications involving the spatially regulated loss, appearance and/or remodelling of distinct sets of cell wall polymers.

Endogenous auxin regulates the sensitivity of Dendrobium (cv. Miss Teen) flower pedicel abscission to ethylene.

Dendrobium flower buds and flowers have an abscission zone at the base of the pedicel (flower stalk). Ethylene treatment of cv. Miss Teen inflorescences induced high rates of abscission in flower buds but did not affect abscission once the flowers had opened. It is not known if auxin is a regulator of the abscission of floral buds and open flowers. The hypotheses that auxin is such a regulator and is responsible for the decrease in ethylene sensitivity were tested. Severed inflorescences bearing 4-8 floral buds and 4-6 open flowers were used in all tests. The auxin antagonists 2,3,5-triiodobenzoic acid (TIBA, an inhibitor of auxin transport) or 2-(4-chlorophenoxy)-2-methyl propionic acid (CMPA, an inhibitor of auxin action) were applied to the stigma of open flowers. Both chemicals induced high flower abscission rates, even if the inflorescences were not treated with ethylene. The effects of these auxin antagonists virtually disappeared when the inflorescences were treated with 1-methylcyclopropene (1-MCP), indicating that the abscission induced by the auxin antagonists was due to ethylene. Removal of the open flowers at the distal end of the pedicel hastened the time to abscission of the remaining pedicel, and also resulted in an increase in ethylene sensitivity. Indole-3-acetic acid (IAA) in lanolin, placed on the cut surface of the pedicel, replaced the effect of the removed flower. Treatments that promoted abscission of open flowers up-regulated a gene encoding a β-1,4-glucanase (Den-Cel1) in the abscission zone (AZ). The abundance of Den-Cel1 mRNA was highly correlated with β-1,4-glucanase activity in the AZ. The results show that auxin is an endogenous regulator of floral bud and flower abscission and suggest that auxin might explain, at least partially, why pedicel abscission of Dendrobium cv. Miss Teen changes from very ethylene-sensitive to ethylene-insensitive.

JOINTLESS suppresses sympodial identity in inflorescence meristems of tomato

Unlike monopodial plants, in which flowering terminates growth of a shoot, plants exhibiting sympodial shoot architecture maintain the potential for indeterminate growth even after converting to floral development. This vegetative indeterminacy is conferred by a special type of axillary meristem, the sympodial meristem, which exhibits precocious but determinate growth. The reiterative formation of sympodial meristems as the plant grows results in a shoot composed of a series of modules, each consisting of a limited number of vegetative nodes and terminated by a flower or inflorescence. To determine how sympodial meristems differ from other shoot meristems, we examined interactions between mutations that affect various shoot meristem types in tomato (Lycopersicon esculentum Mill.). Analysis of double mutant combinations of jointless, lateral suppressor, self-pruning, blind, and anantha showed that sympodial meristems share regulatory features with inflorescence meristems. Genetic studies on the jointless mutation implicated this gene in suppressing sympodial meristem fate in the inflorescence. As this mutation has a second phenotype, the elimination of the pedicel abscission zone, we examined the expression pattern of JOINTLESS to test whether pedicel development is involved in directing shoot architecture. We found that this MADS box gene is expressed in a variety of shoot meristems, including inflorescence, floral, sympodial, and axillary meristems, as well as in early staged floral organs, in sporogenous tissues of anthers, and in ovules. Lack of expression in developing pedicels indicates abscission zone development does not rely on JOINTLESS transcription in the differentiating cells. We conclude that the primary role of JOINTLESS is to suppress sympodial meristem identity in inflorescence meristems.

Involvement of Ethylene in the Pedicel in Preharvest Abscission of 'Tsugaru' Apple

The involvement of ethylene in the pedicel in preharvest fruit drop and the relationship between ethylene in the pedicel and its production in the flesh and the seed were investigated in 'Tsugaru' apple. The induction of pedicel abscission was achieved by the injection of ethylene with a syringe, whereas it was inhibited by 2, 5-norbornadiene (NBD), an antagonist of ethylene action. The injection of ethephon into the fruit core, or the spray on the bourse resulted in increasing ethylene content in the pedicel and subsequent fruit abscission. The treatment with aminoetoxy-vinylglicine (AVG) of the fruit core, the inhibitor of ethylene synthesis, reduced the fruit abscission and ethylene content in the pedicel. Ethylene production of the seed and the flesh, and its content in the pedicel in 'Tsugaru' greatly increased before the rapid increase in fruit drop. Fruit of 'Jonagold' usually do not exhibit preharvest drop, the ethylene production and ethylene content are low; they increased little before harvest. Therefore, ethylene likely originates in the flesh and seeds and is translocated to the pedicel where it acts to induce fruit abscission.

Localization of jointless-2 gene in the centromeric region of tomato chromosome 12 based on high resolution genetic and physical mapping.

Abscission is a universal process whereby plants shed their organs, such as flowers, fruit and leaves. In tomato, the non-allelic mutations jointless and jointless-2 have been discovered as recessive mutations that completely suppress the formation of pedicel abscission zones. A high resolution genetic map of jointless-2 was constructed using 1,122 jointless F2 plants. Restriction fragment length polymorphism (RFLP) marker RPD140 completely co-segregated with the jointless-2 locus and mapped in a 2.4 cM interval between RFLP markers CD22 and TG618. To chromosome walk to jointless-2, all three markers were used to screen a bacterial artificial chromosome (BAC) library and contigs were developed. Intensive efforts to expand and merge the BAC contigs were unsuccessful because of the highly repetitive sequence content on the distal ends of each contig. To determine the physical distance between and the orientation of the three contigs, we used high resolution pachytene fluorescence in situ hybridization (FISH) mapping. The RPD140 contig was positioned in the centromeric region of chromosome 12 between two large pericentric heterochromatin blocks, about 50 Mb from the TG618 contig on the short arm and 10 Mb from the CD22 contig on the long arm, respectively. Based on high resolution genetic and physical mapping, we conclude that the jointless-2 gene is located within or near the chromosome 12 centromere where 1 cM is approximately 25 Mb in length.

Grapevine fruit set: Physiology of the abscission zone

Effects of ethylene and of 'anti-ethylene' compounds on the floral pedicel abscission zone in grapevines were analysed via a laboratory model consisting of isolated flowers held in Petri dishes. Our model permitted precise determination of abscission and enabled us to test a range of physiologically-active compounds including ethylene precursors, and antagonists of ethylene action. For example, a precursor of ethylene, 1-aminocyclopropane-l-carboxylic acid, had the same effect as ethylene in promoting abscission. Conversely, an inhibition of ethylene action by silver thiosulfate or an inhibition of ethylene synthesis by amino-oxyacetic acid both strongly inhibited abscission zone function. The same type of effect can be obtained by increasing the proportion of auxin with regard to ethylene. The abscission zone of the isolated flower pedicel of grapevine conforms to the classic model of hormone-mediated operation of a pre-existing abscission zone. Our definition of hormone regulation holds practical implications for viticulture and offers new possibilities for controlling berry drop.

Genetic mapping of jointless-2 to tomato chromosome 12 using RFLP and RAPD markers

Abscission zones are specialized regions in plants, usually located at the base of most plant parts, such as flowers, fruit and leaves, where organs are shed. Although a great deal of information is known about the physiological and biochemical events that lead to organ shedding, very little is known of the molecular events that lead to the formation of the abscission zone itself. In tomato, two recessive mutations have been discovered that completely suppress the formation of flower and fruit pedicel abscission zones, i.e., jointless (j) and jointless-2 (j-2), both tentatively localized to chromosome 11 about 30 cM apart. Because the study of the control of abscission zone development is important for both basic and applied research we are using a map-based cloning approach to identify the jointless genes. The first step in any positional cloning experiment is to establish segregating mapping populations for the target gene and identify closely linked molecular markers that flank the locus. In this study, bulked segregant analysis was used to identify a RAPD marker associated with the j-2 locus, RPD140. To determine the chromosome location of RPD140, we converted it to an RFLP marker that was then mapped on the Cornell reference tomato map in a marker-dense region of chromosome 12. To verify that the j-2 locus was located on tomato chromosome 12, we used nine chromosome 12 RFLP markers linked with RPD140 to map the j-2 gene in an interspecific F2 mapping population of 151 plants segregating for j-2. The j-2 gene was localized to a 3.0-cM interval between RPD140 and TG618 on tomato chromosome 12.

Spontaneous phloem exudation accompanying abscission in Lupinus mutabilis (Sweet)

Like some of the Mediterranean members of the genus Lupinus, the New World lupin, Lupinus mutabilis (Sweet; cv. Inti), exhibits prolonged (20-40 min) exudation of phloem sap from incisions made in stems, in the raceme and at the tips and sutures of developing fruits. Just prior to or immediately following abscission of flowers of L. mutabilis there was also spontaneous exudation from the proximal face of the abscission zone at the base of the pedicel. This is not a recorded feature of other lupins. Analysis of solutes in this exudate was consistent with its having been derived directly from phloem. The major solutes were sucrose (0.94±0.04 M), amino acids (188±11 mM, 45% as asparagine and 15% as glutamine), K ion (52 mM), and total phosphorus (17 mM). Microscopic examination of the proximal face of the pedicel abscission zone at or following abscission showed little or no breakage of the cells at the zone. The major solutes of spontaneous exudate were similar to those in exudates collected from incisions made in the supporting raceme, upper stem and branches, at the tips and sutures of developing fruits and in the mid- and basal stem regions. However, there were significant compositional differences among minor constituents. The spontaneous exudate had a higher level of Ca ion and, consequently, a narrower Mg/Ca ratio (2.8) than exudate from incisions in the adjacent raceme (9.3) or fruits (15.7). There were also higher concentrations of trace elements (Mn, Zn and Cu) but lower concentrations (3 ng ml -1 ) of cytokinins compared to exudates collected from incisions (20 ng ml -1 ). The relative contents of K and Na ions in exudates from incisions at different sites on the plant showed evidence of selective phloem loading and downward translocation of Na ion and selective loading and upward translocation of K ion.

Interactions between jointless and Wild-Type Tomato Tissues during Development of the Pedicel Abscission Zone and the Inflorescence Meristem

Interactions between jointless and Wild-Type Tomato Tissues during Development of the Pedicel Abscission Zone and the Inflorescence Meristem

Interactions between jointless and wild-type tomato tissues during development of the pedicel abscission zone and the inflorescence meristem.

The jointless mutation of tomato results in the formation of flower pedicels that lack an abscission zone and inflorescence meristems that revert to vegetative growth. We have analyzed periclinal chimeras and mericlinal sectors of jointless and wild-type tissue to determine how cells in different meristem layers (L1, L2, and L3) and their derivatives interact during these two developmental processes. Cells in the inner meristem layer, L3, alone determined whether the meristem maintained the inflorescence state or reverted to vegetative growth. Moreover, L3 derivatives determined whether a functional pedicel abscission zone formed. Limited and disorganized autonomous development of wild-type L2-derived cells occurred when they overlay mutant tissue. Adjacent mutant and wild-type L3-derived tissues in pedicels developed autonomously, indicating little or no lateral communication. Only the outermost L3-derived cells within the pedicel were capable of orchestrating normal pedicel development in overlying tissues, revealing the special status of those cells as coordinators of development for L1- and L2-derived cells, whereas the innermost L3-derived cells developed autonomously but did not influence the development of other cells.

Map-based cloning in crop plants: tomato as a model system II. Isolation and characterization of a set of overlapping yeast artificial chromosomes encompassing the jointless locus.

A map-based cloning technique for crop plants is being developed using tomato as a model system. The target gene jointless is a recessive mutation that completely suppresses the formation of flower and fruit pedicel abscission zones. Previously, the jointless locus was mapped to a 3 cM interval between the two molecular markers TG523 and RPD158. Physical mapping of the jointless region by pulsed-field gel electrophoresis demonstrated that TG523 and RPD158 reside on a 600 kb SmaI fragment. In this study, TG523 was used as a probe to screen a tomato yeast artificial chromosome (YAC) library. Six tomato YAC (TY) clones were isolated, ranging from 220 to 380 kb in size. Genetic mapping of YAC ends demonstrated that this set of overlapping YACs encompasses the jointless locus. Two YAC ends, TY159L (L indicates left end) and TY143R (R indicates right end), cosegregate with the jointless locus. Only one of the six YACs (TY142) contained single-copy DNA sequences at both ends that could be mapped. The two ends of TY142 were mapped to either side of the jointless locus, indicating that TY142 contains a contiguous 285 kb tomato DNA fragment that probably includes the jointless locus. Physical mapping of the TY142 clone revealed that TY159L and TY143R reside on a 55 kb SalI fragment. Southern blot hybridization analysis of the DNAs of tomato lines nearly isogenic for the jointless mutation has allowed localization of the target locus to a region of less than 50 kb within the TY142 clone.

The never ripe mutation blocks ethylene perception in tomato.

Seedlings of tomato fruit ripening mutants were screened for their ability to respond to ethylene. Ethylene induced the triple response in etiolated hypocotyls of all tomato ripening mutants tested except for one, Never ripe (Nr). Our results indicated that the lack of ripening in this mutant is caused by ethylene insensitivity. Segregation analysis indicated that Nr-associated ethylene insensitivity is a single codominant trait and is pleiotropic, blocking senescence and abscission of flowers and the epinastic response of petioles. In normal tomato flowers, petal abscission and senescence occur 4 to 5 days after the flower opens and precede fruit expansion. If fertilization does not occur, pedicel abscission occurs 5 to 8 days after petal senescence. If unfertilized, Nr flowers remained attached to the plant indefinitely, and petals remained viable and turgid more than four times longer than their normal counterparts. Fruit development in Nr plants was not preceded by petal senescence; petals and anthers remained attached until they were physically displaced by the expanding ovary. Analysis of engineered 1-aminocyclopropane-1-carboxylate (ACC) synthase-overexpressing plants indicated that they are phenotypic opposites of Nr plants. Constitutive expression of ACC synthase in tomato plants resulted in high rates of ethylene production by many tissues of the plant and induced petiole epinasty and premature senescence and abscission of flowers, usually before anthesis. There were no obvious effects on senescence in leaves of ACC synthase overexpressers, suggesting that although ethylene may be important, it is not sufficient to cause tomato leaf senescence; other signals are clearly involved.

A basic-type PR-1 promoter directs ethylene responsiveness, vascular and abscission zone-specific expression.

Pathogenesis-related (PR) proteins form a heterogeneous group of host-encoded, low-molecular-mass proteins that are secreted through the exocytic pathway. They are synthesized by the plant in response to various stimuli, including pathogen attack or exposure to certain chemicals. The PRB-1b gene of Nicotiana tabacum codes for a basic-type PR-1 protein whose transcription is regulated by ethylene. A minimal ethylene-responsive promoter element was defined by deletion analysis in transgenic tobacco plants. Promoter sequences containing 213 bp or more were sufficient to enhance a 20-fold increase of beta-glucuronidase reporter gene expression in transgenic tobacco leaves exposed to 20 microliters l-1 of ethylene, while 67 bp were not sufficient to trigger ethylene responsiveness. All the constructs that retained ethylene inducibility exhibited phloem-specific activity, which was constitutive in petiole and pedicel abscission zones. This functional study was correlated to an in vitro screening of the major nuclear proteins' binding sites present on the promoter. Gel-shift analysis using nuclear extracts from ethylene-treated and non-treated plants revealed five sequence-specific protein-DNA complexes on promoter sequences spanning -863 to -142 bp. Constitutive expression of the basic-type PR-1 genes at the leaf and petiole or flower and pedicel interfaces may represent pre-emption of plant defenses against potential pathogens, suggesting a functional similarity to pathogen-induced expression in the leaf.

Application of cytokinins to flowers to increase pod set in Lupinus angustifolius L

Exogenous application of a 2 mol m-3 buffered solution of N6 benzylaminopurine (BAP) to flowers on the main stem inflorescence of Lupinus angustifolius L, cv. Danja profoundly altered reproductive development by reducing post-anthesis abscission of flowers and small pods. The same effect of BAP was recorded for a mutant (abs-) of cv. Danja, in which organ abscission was completely absent, indicating that localized application of cytokinin enhanced reproductive development rather than reduced pedicel abscission per se in the parent line. Application to pedicel and sepals at the open flower stage completely eliminated flower abortion on the main inflorescence, compared with less than 50% pod initiation on untreated inflorescences, more than doubled final pod yield on the main inflorescence and increased the number of mature pods on the whole plant by 33%. A single dose of BAP, to an inflorescence which bore flowers ranging in their stage of development from post-anthesis to immature flower buds, significantly increased the number of pods initiated and at final harvest, measured on a per plant basis. A number of synthetic and naturally occurring cytokinins, including zeatin riboside and dihydrozeatin riboside, were also effective. BAP application induced a longer period of flowering and resulted in a considerably thickened raceme. This was most marked at the distal end which showed enhanced cambial development and secondary vascularization compared with untreated controls. The positive effects of BAP application on pod initiation were not restricted to cv. Danja but were found also for cv. Warrah and cv. Gungurru, both of which have enhanced pod set compared with Danja. Enhanced pod initiation on the main inflorescence generally reduced the number of pods developing on branch inflorescences. Additional application of BAP to flowers on branches, even at the most opportune time and at the most effective site, did not enhance pod initiation and, in some cases, significantly reduced pod set on these branches. The data indicate that it would be very difficult to exploit the positive effect of exogenous cytokinin application on pod set in field crops of lupin. However, selection or genetic engineering of plants with higher levels of endogenous cytokinins in flowers or flower parts at anthesis may provide a means by which to assess the importance of this factor in determining yield stability.

Pedicel abscission and rachis morphology of soybean as influenced by benzylaminopurine and the presence of pods

The cytokinin 6-benzylaminopurine (BAP) increases pod set of soybean Glycine max (L.) Merr. This study was performed to determine the effect of site and method of BAP application on pedicel abscission and the accompanying changes in rachis anatomy. Spraying racemes with BAP in solution, or applying in a lanolin suspension to proximal nodes on a rachis where proximal pedicels had been excised, delayed pedicel abscission at distal nodes. Applying BAP in lanolin to distal pedicels following flower excision failed to delay their abscission. BAP caused rachis swelling only when pods were present, but BAP could delay pedicel abscission either in the presence or absence of pods. These results suggest that rachis swelling following BAP treatment does not have a causal relationship to a delay or decrease of pedicel abscission.

Pedicel abscission of soybean: cytological and ultrastructural changes induced by auxin and ethephon

Indole-3-acetic acid delayed the onset of pedicel abscission of soybean, Glycine max (L.) Merrill, by 20 h, and in some experiments, significantly reduced abscission over a 7-day treatment period. Cytological and ultrastructural development of the abscission zone could be divided into two phases: the first associated with longer cells and fewer multigrained amyloplasts in the incipient separation layer; the second with shorter cells (indicative of secondary cell division), increased numbers of amyloplasts, and significant changes in the percent volume of cytoplasm, vacuoles, and wall tissue. Middle lamella dissolution preceded cell separation. Indole-3-acetic acid delayed but did not disrupt the sequence of events leading to abscission. Ethephon treatment hastened abscission but both delayed and disrupted typical abscission events, especially secondary cell division, which occured less frequently. In addition, cellular collapse and greater swelling of cells were observed in the separation layer of ethephon-treated tissue. Key words: abscission, ethylene, Glycine max, indole-3-acetic acid, pedicel, raceme.

Screening Pepper Cultivars for Resistance to Flower Abscission: A Comparison of Techniques

In one greenhouse and two field experiments, eight or ten pepper (Capsicum annuum L.) cultivars were subjected to low-light stress by use of shade cloth (reducing light by 80%) or to foliar sprays of ethephon at 75 or 150 pi-liter-]. Both low-light stress and ethephon identified `Ace', 'Canape', and. `Belrubi' as less susceptible to flower and flower bud abscission than other cultivars in the first field experiment. In the 2nd year, air mean maxima of 32C caused severe abscission in controls and shaded plants, and complete loss of flowers in those sprayed with ethephon. Abscission of disbudded pedicels was not related to abscission susceptibility of eight cultivars when subjected to shade. While ethephon spray can serve as a satisfactory abscission screening tool under unstressed growing conditions, low-light stress imposed by shading may be used under a wider range of conditions. Chemical name used: 2-chloroethyl phosphoric acid (ethephon).

Hormonal Basis for Low Light Intensity-induced Flower Bud Abscission of Pepper

Abstract A series of field and greenhouse experiments was conducted with three cultivars of bell pepper (Capsicum annuum L.) to determine the hormonal basis for flower bud and flower abscission as induced by low light intensity (LLI). Imposition of 80% shade for 6 days increased abscission of reproductive structures by 38% and resulted in an increase in bud ethylene production. Concomitantly, bud reducing sugars and sucrose decreased and these were negatively correlated with ethylene levels and those of its precursor, ACC. Infusion of ACC into the pedicel resulted in flower bud abscission within 48 hr. The results indicate that ethylene is the primary causal agent of pepper flower bud abscission. Production of auxin by the bud plays a role in prevention of abscission. The abscission of disbudded pedicels was prevented by infusion of NAA. Although the three cultivars had similar responses to ACC, they differed in the amount of abscission under stress, bud sugar levels, and the time of onset of ACC and ethylene production. Chemical names used: 1-aminocyclopropane-1-carboxylic acid (ACC); α-napthaleneacetic acid (NAA); (2-chloro-ethyl)phosphonic acid (ethephon).