Effects of Drought and Defoliation on Bud Viability in Two Caespitose Grasses

Axillary bud number, bud respiratory activity, and photosyntheticcanopy re-establishment after defoliation were determined fortwo bunchgrass species, Agropyron desertorum and Agropyron spicatum,which were exposed to draughted, natural or irrigated conditions.These field treatments were repeated annually on the same plantsfor the period 1984–1986. Bud respiratory activity wasexamined using the tetrazolium test, which was validated withthe vital stain Evan's blue, at the end of the study In spring of the third year, the number of axillary buds ontillers of both species was lowest in the drought treatment.Most of these buds, and those observed immediately after defoliationin 1985, were metabolically active. These results indicate thatafter mid-season defoliation under drought, when no re-growthoccurred, the re-growth capacity was not limited by bud numberor viability. After 3 years of defoliation, tiller number andgrowth in both species were reduced in the following springunder all water regimes. This reduction was present 1 year earlierin the drought treatment than in the treatments with higherwater availability. Permanent dormancy or death of the replacementaxillary meristems can explain this plant response. Continueddefoliation of the tillers under drought would reduce the photosyntheticarea further, and probably affect the persistence of these speciesin the community Agropyron desertorum, Agropyron spicatum, crested wheatgrass, bluebunch wheatgrass, drought, defoliation, re-growth, bud viability, tetrazolium, Evan's blue     

Effect of Severity of Defoliation on the Viability of Reproductive and Vegetative Axillary Buds of Trifolium repens L.

This glasshouse experiment was performed to assess the effectsof a range of constant defoliation regimes applied to cuttingsof a single large-leaved genotype ofTrifolium repens L. on theviability of its axillary buds. Plants were established to comprisea single main stolon (axillary branches were removed) and defoliationtreatments were applied by removing the older (basal) leavesuntil leaf complements of 1·0, 1·5, 2·0,2·5, 3·0 or all leaves (control) remained. Basalleaves were subsequently removed as necessary to maintain thetarget leaf complements. Only severe defoliation (leaf complements of 1·0 and1·5) induced a loss of viability in axillary buds. Lossof viability was greatest in reproductive buds present withinthe apical bud when the treatments were first imposed. Althoughthe most severe treatment (leaf complement 1·0) resultedin death of half the plants, in plants surviving that treatment,death of vegetative axillary buds was restricted to 21% of thevegetative buds at the three youngest node positions withinthe apical bud at the time of treatment application. No othertreatment induced any loss of viability of vegetative buds.There was no loss of viability of axillary buds at nodes formedafter the treatments were imposed. The frequency of initiationof inflorescences at nodes formed after treatments were imposeddecreased as defoliation severity increased. Severe defoliation resulted in marked changes in plant morphologyindicative of a sharp decrease in availability of intraplantresources. It was concluded that under severe defoliation: (1)the potential for vegetative growth (as represented by viablevegetative axillary buds) was maintained at the expense of reproductivegrowth; and (2) that the loss of viability of axillary budswas associated with the sudden changes in physiological processesinduced by defoliation as there was no loss of viability inbuds formed after plants had adjusted their phenotype to oneof smaller size. Trifolium repens L.; white clover; defoliation; axillary buds; viability; inflorescences     

Axillary bud banks of two semiarid perennial grasses: occurrence, longevity, and contribution to population persistence

The occurrence, longevity, and contribution of axillary bud banks to population maintenance were investigated in a late-seral perennial grass, Bouteloua curtipendula, and a mid-seral perennial grass, Hilaria belangeri, in a semiarid oak-juniper savanna. Axillary buds of both species were evaluated over a 2-year period in communities with contrasting histories of grazing by domestic herbivores. A double staining procedure utilizing triphenyl tetrazolium chloride and Evan's blue indicated that both viable and dormant axillary buds remained attached to the base of reproductive parental tillers for 18–24 months which exceeded parental tiller longevity by approximately 12 months. Bud longevity of the late-seral species, B. curtipendula, exceeded bud longevity of the mid-seral species, H. belangeri, by approximately 6 months. Younger buds located on the distal portion of the tiller base were 3.2 and 1.4 times more likely to grow out than older proximal buds of B. curtipendula and H. belangeri, respectively. The percentage of older proximal buds, which included comparable portions of viable and dormant buds, that grew out to produce tillers following mortality of parental tillers was 6.0% for B. curtipendula and 8.4% for H. belangeri. In spite of the occurrence of relative large axillary bud banks for both species, the magnitude of proximal bud growth did not appear sufficient to maintain viable tiller populations. We found no evidence to support the hypothesis of compensatory bud growth on an individual tiller basis for either species. Grazing history of the communities from which the buds were collected did not substantially affect the number, status, longevity, or outgrowth of axillary buds on an individual tiller basis for either species. However, long-term grazing by domestic herbivores influenced axillary bud availability by modifying population structure of these two species. Bud number per square meter for B. curtipendula was 25% lower in the long-term grazed compared to the long-term ungrazed community based on a reduction in both tiller number per plant and plant number per square meter. In contrast, bud number per square meter for H. belangeri was 190% greater in the long-term grazed than in the long-term ungrazed community based on a large increase in plant density per square meter. Minimal contributions of axillary bud banks to annual maintenance of tiller populations in this mid- and late-seral species underscores the ecological importance of consistent tiller recruitment from recently developed axillary buds. Consistent tiller recruitment in grasslands and savannas characterized by intensive grazing and periodic drought implies that (1) bud differentiation and maturation must be remarkably tolerant of adverse environmental conditions and/or (2) tiller recruitment may resume from buds that mature following the cessation of severe drought and/or grazing, rather than from mature buds that survive these disturbances. These scenarios warrant additional research emphasis given the critical importance of this demographic process to tiller replacement in species populations and the maintenance of relative species abundance in grasslands and savannas. Received: 12 August 1996 / Accepted: 30 December 1996     

Role of polarity in de novo shoot bud initiation from stem disc explants of <Emphasis Type="Italic">Curculigo orchioides</Emphasis> Gaertn. and its encapsulation and storability

The occurrence of strong polarity towards shoot bud induction and the effect of cytokinin(s) on each segment of stem axis, encapsulation and storability of de novo Shoot buds of Curculigo orchioides Gaertn. (Hypoxidaceae) have been documented in the present communication. Maximum number of shoot buds arising de novo from the stem discs (cross section) explanted from proximal end on MS medium fortified with BAP and KIN 1 mg/L each. Stem discs from distal end were less efficient in shoot bud induction. A combination of two cytokinins (BAP and KIN) as a synergistic effect on shoot buds induction from each segment of stem axis. Stem discs in inverted position produced shoot buds from the lower surface, showing strong polarity within the explant. Further, storability and shoot development of sodium alginate encapsulated shoot buds of Curculigo orchioides were tested on half-strength Murashige and Skoog (MS) basal medium fortified with coconut water (10% v/v). The frequency of regeneration from encapsulated shoot buds was affected significantly by concentration of sodium alginate and the duration of exposure to calcium chloride. Shoot buds encapsulated with 2.5% sodium alginate dissolved in MS basal salts solution recorded significantly higher shoot development than other treatments. A relatively short (5 min) incubation with calcium chloride solution provided uniform encapsulation of shoot buds that gave the highest percentage (68%) of shoot development. Encapsulated shoot buds could be stored at 4°C for 50 days without reduction in viability as oppose to non-encapsulated shoot buds, which showed 9.5% viability after 20 days at 4°C. Encapsulated shoot bud developed into normal shoots. Based on the present observations an improved protocol may be developed for the rapid multiplication and conservation of the endangered species—C. orchioides.     

Trehalose 6‐phosphate is involved in triggering axillary bud outgrowth in garden pea (Pisum sativum L.)

Trehalose 6‐phosphate (Tre6P) is a signal of sucrose availability in plants, and has been implicated in the regulation of shoot branching by the abnormal branching phenotypes of Arabidopsis (Arabidopsis thaliana) and maize (Zea mays) mutants with altered Tre6P metabolism. Decapitation of garden pea (Pisum sativum) plants has been proposed to release the dormancy of axillary buds lower down the stem due to changes in sucrose supply, and we hypothesized that this response is mediated by Tre6P. Decapitation led to a rapid and sustained rise in Tre6P levels in axillary buds, coinciding with the onset of bud outgrowth. This response was suppressed by simultaneous defoliation that restricts the supply of sucrose to axillary buds in decapitated plants. Decapitation also led to a rise in amino acid levels in buds, but a fall in phosphoenolpyruvate and 2‐oxoglutarate. Supplying sucrose to stem node explants in vitro triggered a concentration‐dependent increase in the Tre6P content of the buds that was highly correlated with their rate of outgrowth. These data show that changes in bud Tre6P levels are correlated with initiation of bud outgrowth following decapitation, suggesting that Tre6P is involved in the release of bud dormancy by sucrose. Tre6P might also be linked to a reconfiguration of carbon and nitrogen metabolism to support the subsequent growth of the bud into a new shoot.     

Fire Effects on Bud Viability and Growth of Stipa tenuis in Semiarid Argentina

Numbers of total, metabolically active, dormant or dead axillarybuds, and growth characteristics were determined before andafter controlled burnings in Stipa tenuis Phil., a native foragegrass of the Caldén District in central Argentina. One-hectareplots were burned on 25 Mar. (Burn 1) or 4 Apr. 1991 (Burn 2),or remained unburned (control). Bud metabolic activity was examinedusing the tetrazolium test and the vital stain Evans' blue. Before fire, more than 83% of the axillary buds on previous-seasonstems of S. tenuis were metabolically active in all treatments.After fire, previous-season stems that produced tiller in thecontrol and Burn 2 plots had more than 75% of the axillary budsalive, but those that did not produce them had more than 82%of their axillary buds dead in the burned areas. This high budmortality was associated with direct fire effects on the fateof buds; most dead buds showed visible signs of dehydration.Since more than 97% of the plant stem bases did not producetillers after fire, tiller number per plant was reduced (P <0·05) in the burned plots to fewer than 22% of valuesof controls. Plant mortality was 50% higher at the Burn 1 thanat the Burn 2 site probably because the first site had a 43%lower soil moisture content (P < 0·05). At the endof the growing season, however, a different set of S. tenuisplants at both burned sites had a similar tiller number anddry weight to controls. These plants were probably in areasof lighter fuel loads and exposed to a less intense fire.Copyright1993, 1999 Academic Press Stipa tenuis Phil., thin needlegrass, controlled burning, bud viability, axillary meristems, regrowth     

Bud banks of perennial savanna grasses in Botswana

Three semi‐arid savanna grasses in Botswana (Stipagrostis uniplumis, Eragrostis lehmanniana, and Aristida stipitata) were sampled to quantify their belowground bud banks during the dormant season and to estimate their relative allocation to vegetative and sexual reproduction. Bud banks of these African perennial caespitose grasses were also compared with four perennial caespitose grasses of semi‐arid North American grasslands. The three African grasses each maintained approximately two buds per tiller and showed a high percentage (88–99%) of tillers producing seed. Only E. lehmanniana produced new aerial tillers from axillary buds at elevated nodes on the stem as well as from the belowground bud bank. Compared with species of North American grasslands, these African grasses produced fewer belowground buds but showed a much higher percentage of tillers producing seed. These patterns indicate relatively greater belowground meristem limitation, lower allocation to vegetative reproduction (tillering) and higher allocation to seed reproduction in these African grasses, although studies of more species are needed to assess the generality of this pattern. The management of savannas in ways that favour the maintenance of a reserve population of belowground buds may increase the ability of grasses to respond to pulses of resource availability, increase their compensatory growth capacity following grazing or drought, and decrease the invasibility of these plant communities by exotic species, whereas maintaining allocation to sexual reproduction may be important for conserving genetic variation and enhancing their capacity to adapt to environmental change.     

Clonal Growth of White Clover: Factors Influencing the Viability of Axillary Buds and the Outgrowth of a Viable Bud to Form a Branch

The development of an axillary bud of white clover to form abranch depends on (1) the bud being viable, vegetative and non-dormant,and (2) suitable conditions for outgrowth of the bud. Foragingtheory emphasises the second of these requirements. Glasshousestudies with white clover rarely result in a loss of bud viability.In contrast, in field populations over 50% of the buds reachingthe stage of maturity when branching can occur are not in aviable, vegetative, non-dormant condition. We examined whethernon-viability could be induced in a glasshouse experiment byapplying treatments in a factorial design. The factors were:defoliation, phosphorus supply, soil moisture status, simulatedtreading and grass competition. In addition, we measured theeffects of the treatments on the outgrowth of viable buds inorder to assess whether the same factors were determining viabilityand outgrowth. Defoliation significantly reduced bud viability(by 44%) but no other factors, either singly or in combination,had a significant effect. A greater variety of factors and combinationsof factors influenced bud outgrowth; these were defoliation,phosphorus status and interactions involving phosphorus andgrass; defoliation, phosphorus and soil moisture; and soil moisture,grass and treading. For white clover it is relevant to includethe state of the axillary meristem in any model of foraging. Trifolium repens ; white clover; axillary bud; viability; clonal growth; foraging; defoliation     

Photosynthetic leaf area modulates tiller bud outgrowth in sorghum

Shoot branches or tillers develop from axillary buds. The dormancy versus outgrowth fates of buds depends on genetic, environmental and hormonal signals. Defoliation inhibits bud outgrowth indicating the role of leaf‐derived metabolic factors such as sucrose in bud outgrowth. In this study, the sensitivity of bud outgrowth to selective defoliation was investigated. At 6 d after planting (6 DAP), the first two leaves of sorghum were fully expanded and the third was partially emerged. Therefore, the leaves were selectively defoliated at 6 DAP and the length of the bud in the first leaf axil was measured at 8 DAP. Bud outgrowth was inhibited by defoliation of only 2 cm from the tip of the second leaf blade. The expression of dormancy and sucrose‐starvation marker genes was up‐regulated and cell cycle and sucrose‐inducible genes was down‐regulated during the first 24 h post‐defoliation of the second leaf. At 48 h, the expression of these genes was similar to controls as the defoliated plant recovers. Our results demonstrate that small changes in photosynthetic leaf area affect the propensity of tiller buds for outgrowth. Therefore, variation in leaf area and photosynthetic activity should be included when integrating sucrose into models of shoot branching.     

Revisiting the fate of buds: size and position drive bud mortality and bursting in two coexisting Mediterranean Quercus species with contrasting leaf habit

Understanding the relationships between bud size and position and bud fate through time is crucial for identifying and subsequently modeling the mechanisms underlying tree architecture. However, there is a lack of information on how bud size drives crown architectural patterns in coexisting tree species. We studied bud demography in two coexisting Mediterranean oak species with contrasting leaf habit (Quercus ilex, evergreen; Q. faginea, deciduous). The main objective was to analyse the effect of bud size on the fate of buds with different positions along the shoot (apical, leaf axillary and scale-cataphyll axillary buds). The number, length and position of all buds and stems were recorded in marked branches during 4 years. Study species presented different strategies in bud production and lifespan. The evergreen species showed greater mortality rate than the deciduous one, which produced larger buds. Bud size and position were highly related since apical buds where longer than axillary ones and bud length declined basipetally along the stem. Apical buds had also higher chances of bursting than axillary ones. Within positions, longer buds presented a higher probability of bursting than shorter ones, although no absolute size threshold was found below which bud bursting was impaired. In Q. ilex, four-year-old buds were still viable and able to burst, whereas in Q. faginea practically all buds burst in their first year or died soon after. Such different bud longevities may indicate contrasting strategies in primary growth between both species. Q. ilex is able to accumulate viable buds for several ages, whereas Q. faginea seems to rely on the production of large current-year buds with high bursting probability under favourable environmental conditions.     

Density-dependent regulation of ramet recruitment by the red:far-red ratio of solar radiation: a field evaluation with the bunchgrass Schizachyrium scoparium

Depressions in the red to far-red ratio (R:FR) of solar radiation arising from the selective absorption of R (600–700 nm) and scattering of FR (700–800 nm) by chlorophyll within plant canopies may function as an environmental signal directly regulating axillary bud growth and subsequent ramet recruitment in clonal plants. We tested this hypothesis in the field within a single cohort of parental ramets in established clones of the perennial bunchgrass, Schizachyrium scoparium. The R:FR was modified near leaf sheaths and axillary buds at the bases of individual ramets throughout the photoperiod without increasing photosynthetic photon flux density (PPFD) by either (1) supplementing R beneath canopies to raise the naturally low R:FR or (2) supplementing FR beneath partially defoliated canopies to suppress the natural R:FR increase following defoliation. Treatment responses were assessed by simultaneously monitoring ramet recruitment, PPFD and the R:FR beneath individual clone canopies at biweekly intervals over a 12-week period. Neither supplemental R nor FR influenced the rate or magnitude of ramet recruitment despite the occurrence of ramet recruitment in all experimental clones. In contrast, defoliation with or without supplemental FR beneath clone canopies reduced ramet recruitment 88% by the end of the experiment. The hypothesis stating that the R:FR signal directly regulates ramet recruitment is further weakened by evidence demonstrating that (1) the low R:FR-induced suppression of ramet recruitment is only one component of several architectural modifications exhibited by ramets in response to the R:FR signal (2) immature leaf blades, rather than leaf sheaths or buds, function as sites of R:FR perception on individual ramets, and (3) increases in the R:FR at clone bases following partial canopy removal are relatively transient and do not override the associated constraints on ramet recruitment resulting from defoliation. A depressed R:FR is probably of greater ecological significance as a signal of competition for light in vegetation canopies than as a density-dependent signal which directly regulates bud growth and ramet recruitment.     

Micropropagation of <Emphasis Type="Italic">Pinus massoniana</Emphasis> and mycorrhiza formation in vitro

A protocol was developed for the micropropagation of Pinus massoniana and mycorrhiza formation on rooted microshoots. Seedling explants were first cultured on Gresshoff and Doy (GD) medium supplemented with 6-benzyladenine (BA) alone or in combination with α-napthaleneacetic acid (NAA) to stimulate the formation of intercotyledonary axillary buds. The frequency of axillary bud induction was up to 97% on medium supplemented with 4.0 mg l⁻¹ BA and 0. 2 mg l⁻¹ NAA, and the average number of buds per explant reached up to 5.5 on medium with 4.0 mg l⁻¹ BA and 0.1 mg l⁻¹ NAA. Axillary buds elongated rapidly after being transferred to half-strength GD medium containing activated charcoal (0.1% w/v). Shoot proliferation was achieved by cutting elongated shoots into stem segments and subculturing on GD medium containing 2 mg l⁻¹ BA and 0.2 mg l⁻¹ NAA. Root primordia were induced in 82% of shoots when transferred to half-strength GD medium containing 0.2 mg l⁻¹ NAA. Root elongation was achieved in a hormone-free GD agar medium or a perlite substrate. Rooted plantlets were inoculated with the mycelium of ectomycorrhizal fungus Pisolithus tinctorius and the formation of ectomycorrhiza-like structures was achieved in vitro.     

Patatin and four serine proteinase inhibitor genes are differentially expressed during potato tuber development

A highly efficient and synchronousin vitro tuberization system is described. One-node stem pieces from potato (Solanum tuberosum cv. Bintje) plants grown under short day-light conditions containing an axillary bud were cultured in the dark on a tuber-inducing medium. After 5 or 6 days all axillary buds started to develop tubers. To study gene expression during tuber development, RNA isolated from tuberizing axillary buds was used for bothin vitro translation and northern blot hybridizations. The genes encoding the proteinase inhibitors I and II (PI-I and PI-II), a Kunitz-and a Bowman-Birk-type proteinase inhibitor were already expressed in uninduced axillary buds. The length of the day-light conditions differently influenced the expression level of the individual genes. In addition, the expression of each of these genes changed specifically during the development of the axillary bud to tuber. In contrast to the expression of these proteinase inhibitor genes, patatin gene expression was only detectable from the day tuberization was manifested as a radial expansion of the axillary bud.These results are discussed with respect to the regulation of the expression of the genes studied in relation to the regulation of tuber development.     

Bud Structure in Relation to Shoot Morphology and Position on the Vegetative Annual Shoots of Juglans regia L. (Juglandaceae)

The length and basal diameter of all lateral and terminal budsof vegetative annual shoots of 7-year-oldJuglans regia treeswere measured. All buds were dissected and numbers of cataphylls,embryonic leaves and leaf primordia were recorded. Each axillarybud was ranked according to the position of its associated leaffrom the apex to the base of its parent shoot. Bud size andcontent were analysed in relation to bud position and were comparedwith the size and number of leaves of shoots in equivalent positionswhich extended during the following growing season. Length andbasal diameter of axillary buds varied according to their positionon the parent shoot. Terminal buds contained more embryonicleaves than any axillary bud. The number of leaves was smallerfor apical and basal axillary buds than for buds in intermediatepositions on the parent shoot only. All new extended shootswere entirely preformed in the buds that gave rise to them.Lateral shoots were formed in the median part of the parentshoot. These lateral shoots derived from buds which were largerthan both apical and basal ones. Copyright 2001 Annals of BotanyCompany Juglans regia L., Persian walnut tree, branching pattern, preformation, bud content, shoot morphology     

Branch growth and leaf numbers of red maple (Acer rubrum L.) and red oak (Quercus rubra L.): response to defoliation

Summary Branch growth and leaf formation from terminal and from lateral buds of red maple (Acer rubrum L.) and red oak (Quercus rubra L.) were measured in response to simulated insect defoliation. A single large branch representative of the crown of each tree was used for enumeration of growth and of bud numbers throughout three successive years of 0, 50, 75, and 100% leaf removal for the entire tree. Leaf number per tree for both species after the last year of defoliation was reduced in direct proportion to the severity of defoliation, in comparison to the predefoliation status of the trees. Bud number per tree for red maple, but not for red oak, was also reduced in proportion to severity of defoliation.Averaged over all defoliation treatments, defoliation reduced branch growth more than leaf production. Furthermore, the reduction in branch growth and leaf production was greater in red oak than in red maple. Three years of successive defoliation reduced the mean lateral plus terminal branch growth by 40% in red oak and by 23% in red maple, while leaf number was reduced 22% in red oak and remained unchanged in red maple. In red maple, 100% defoliation caused greater branch death than the 50 or 75% defoliation treatments, and the amount of death was greater after each successive year of defoliation. In contrast to red maple, undefoliated red oak incurred a substantial amount of branch death throughout the study which was little affected by defoliation treatment.     

Effect of Assimilate Supply on Development and Growth Potential of Axillary Buds in Roses

The effect of assimilate supply on axillary bud developmentand subsequent shoot growth was investigated in roses. Differencesin assimilate supply were imposed by differential defoliation.Fresh and dry mass of axillary buds increased with increasedassimilate supply. The growth potential of buds was studiedeither by pruning the parent shoot above the bud, by graftingthe bud or by culturing the bud in vitro. Time until bud breakwas not clearly affected by assimilate supply during bud development,Increase in assimilate supply slightly increased the numberof leaves and leaf primordia in the bud; the number of leavespreceding the flower on the shoot grown from the axillary budsubstantially increased. No difference was found in the numberof leaves preceding the flower on shoots grown from buds attachedto the parent shoot and those from buds grafted on a cutting,indicating that at the moment of release from inhibition thebud meristem became determined to produce a specific numberof leaves and to develop into a flower. Assimilate supply duringaxillary bud development increased the number of pith cells,but the final size of the pith in the subsequent shoot was largelydetermined by cell enlargement, which was dependent on assimilatesupply during shoot growth. Shoot growth after release frominhibition was affected by assimilate supply during axillarybud development only when buds sprouted attached to the parentshoot, indicating that shoot growth is, to a major extent, dependenton the assimilate supply available while growth is taking place.Copyright1994, 1999 Academic Press Assimilate supply, axillary bud, cell number, cell size, defoliation, development, growth potential, meristem programming, pith, Rosa hybrida, rose, shoot growth     

Vegetative axillary bud dormancy induced by shade and defoliation signals in the grasses

Vegetative axillary bud dormancy and outgrowth is regulated by several hormonal and environmental signals. In perennials, the dormancy induced by hormonal and environmental signals has been categorized as eco-, endo- or para-dormancy. Over the past several decades para-dormancy has primarily been investigated in eudicot annuals. Recently, we initiated a study using the monoculm phyB mutant (phyB-1) and the freely branching near isogenic wild type (WT) sorghum (Sorghum bicolor) to identify molecular mechanisms and signaling pathways regulating dormancy and outgrowth of axillary buds in the grasses. In a paper published in the January 2010 issue of Plant Cell and Environment, we reported the role of branching genes in the inhibition of bud outgrowth by phyB, shade and defoliation signals. Here we present a model that depicts the molecular mechanisms and pathways regulating axillary bud dormancy induced by shade and defoliation signals in the grasses.Key words: axillary bud, dormancy, shade, phytochrome, defoliation, shoot branching, teosinte branched1, MAX2, cell cycle, sorghumThe dormancy and outgrowth of axillary buds is regulated by several plant hormones such as auxin, cytokinins, abscisic acid and strigolactones, and by environmental factors such as light quality, quantity and duration as well as water, temperature and nutrient status.^1–3 Since the fate of an axillary bud is regulated by such diverse hormonal and environmental signals and their interactions, the type of dormancy induced varies. In perennials, three types of bud dormancy have been identified.^4,5 Dormancy mediated by factors within the bud is known as endo-dormancy; while dormancy induced by factors within the plant but outside the bud is called paradormancy or correlative inhibition; the best known example being apical dominance. Dormancy induced due to unfavorable environmental conditions is known as eco-dormancy. Although there is an indepth knowledge about para-dormancy in annuals,⁶ few studies have been conducted on eco-dormancy. Similarly, studies of endo-dormancy have largely been restricted to low-temperature mediated growth-cessation of axillary buds of perennial plants.^7,8 To understand the regulation of dormancy and outgrowth of axillary buds in monocots, we initiated a study on the molecular mechanisms inhibiting bud outgrowth by shade and defoliation signals in sorghum. Our results published in the January 2010 issue of Plant, Cell & Environment indicate that different types of dormancy may be induced in axillary buds of annual grasses by various signals and there may be overlapping and independent molecular mechanisms mediating induction of axillary bud dormancy.     

Effect of Cutting During Reproductive Development on the Regrowth and Regenerative Capacity of the Perennial Grass, Phalaris aquatica L., in a Controlled Environment

Two cultivars of phalaris (Phalaris aquatica L.), Australianand Sirolan, were cut at four stages of development in a controlledenvironment to study factors involved in the sensitivity ofphalaris to grazing during spring. Effects on tillering, regrowthafter cutting and regenerative capacity after an artificiallyimposed summer dormant period were observed. Compared with Australian,Sirolan cut after the commencement of stem elongation was characterizedby a higher degree of decapitation due to more synchronous elevationof its apices, and displayed a more severe reduction in regrowth,size of tiller bases and dormant buds and levels of carbohydratereserves in summer relative to plants cut before stem elongation.Suppressed bud activity in tillers of Sirolan decapitated atearly stem elongation, and the potential for profuse tilleringassociated with low bud dormancy after cutting at the earlyboot stage, could reduce persistence under field conditions. Relative to plants cut before stem elongation, regenerationgrowth after 'summer' by plants cut during reproductive developmentwas depressed more severely for Sirolan (56-70%; P 0·05)than Australian (28%; n.s), a result more closely related toregenerating tiller size than number. Regeneration growth didnot differ significantly with stage reproductive developmentat cutting in either cultivar. Regenerative capacity of phalariscut during reproductive development can be considered to dependon an increasing contribution from buds on bases of tillersdecapitated when cut and a contribution from buds on intacttiller bases which declines as the stage of cutting becomeslater. The balance between these source will depend on the environment.Copyright1993, 1999 Academic Press Phalaris aquatica L., phalaris, regrowth, persistence, defoliation, cutting, perennial grass, tillering     

Suppression of sorghum axillary bud outgrowth by shade, phyB and defoliation signalling pathways

In recent years, several genetic components of vegetative axillary bud development have been defined in both monocots and eudicots, but our understanding of environmental inputs on branching remains limited. Recent work in sorghum ( Sorghum bicolor ) has revealed a role for phytochrome B (phyB) in the control of axillary bud outgrowth through the regulation of Teosinte Branched1 ( TB1 ) gene. In maize ( Zea mays ), TB1 is a dosage-dependent inhibitor of axillary meristem progression, and the expression level of TB1 is a sensitive measure of axillary branch development. To further explore the mechanistic basis of branching, the expression of branching and cell cycle-related genes were examined in phyB-1 and wild-type sorghum axillary buds following treatment with low-red : far-red light and defoliation. Although defoliation inhibited bud outgrowth, it did not influence the expression of sorghum TB1 ( SbTB1 ), whereas changes in SbMAX2 expression, a homolog of the Arabidopsis ( Arabidopsis thaliana ) branching inhibitor MAX2 , were associated with the regulation of bud outgrowth by both light and defoliation. The expression of several cell cycle-related genes was also decreased dramatically in buds repressed by defoliation, but not by phyB deficiency. The data suggest that there are at least two distinct molecular pathways that respond to light and endogenous signals to regulate axillary bud outgrowth.     

Effect of plant growth substances on the growth of axillary buds in cultured stem segments of Phaseolus vulgaris L.

The hormonal control of axillary bud growth was investigated in cultured stem segments of Phaseolus vulgaris L. When the stem explants were excised and implanted with their apical end in a solid nutrient medium, outgrowth of the axillary buds-located at the midline of the segment-was induced. However, if indoleacetic acid (IAA) or naphthaleneacetic acid (NAA) was included in the medium, bud growth was inhibited. The exposure of the apical end to IAA also caused bud abscission and prevented the appearance of new lateral buds.In contrast to apically inserted segments, those implanted in the control medium with their basal end showed much less bud growth. In these segments, the auxin added to the medium either had no effect or caused a slight stimulation of bud growth.The IAA transport inhibitor N-1-naphthylphthalamic acid (NPA) relieved bud growth inhibition by IAA. This suggests that the effect of IAA applied at the apical end requires the transport of IAA itself rather than a second factor. With the apical end of the segment inserted into the IAA-containing medium, simultaneous basal application of IAA relieved to some extent the inhibitory effect of the apical IAA treatment. These results, together with data presented in a related article [Lim R and Tamas I (1989) Plant Growth Regul 8: 151–164], show that the polarity of IAA transport is a critical factor in the control of axillary bud growth.Of the IAA conjugates tested for their effect on axillary bud growth, indoleacetyl alanine, indoleacetic acid ethyl ester, indoleacetyl-myo-inositol and indoleacetyl glucopyranose were strongly inhibitory when they were applied to the apical end of the stem explants. There was a modest reduction of growth by indoleacetyl glycine and indoleacetyl phenylalanine. Indoleacetyl aspartic acid and indoleglyoxylic acid had no effect.In addition to IAA and its conjugates, a number of other plant growth substances also affected axillary bud growth when applied to the apical end of stem segments. Myo-inositol caused some increase in the rate of growth, but it slightly enhanced the inhibitory effect of IAA when the two substances were added together. Gibberellic acid (GA₃) caused some stimulation of bud growth when the explants were from younger, rather than older plants. The presence of abscisic acid (ABA) in the medium had no effect on axillary bud growth. Both kinetin and zeatin caused some inhibition of axillary buds from younger plants but had the opposite effect on buds from older ones. Kinetin also enhanced the inhibitory effect of IAA when the two were applied together.In conclusion, axillary buds of cultured stem segments showed great sensitivity to auxins and certain other substances. Their growth responded to polarity effects and the interaction among different substances. Therefore, the use of cultured stem segments seems to offer a convenient, sensitive and versatile test system for the study of axillary bud growth regulation.